CRISPRimmunity

Overview of predicted results

Overview of the results

Contig_ID	Contig_def	CRISPR array number	Contig Signature genes	Self targeting spacer number	Target MGE spacer number	Prophage number	Anti-CRISPR protein number
NZ_LN831776	Paenibacillus riograndensis SBR5 isolate SBR5(T) chromosome I	80 crisprs	RT,PrimPol,cas14j,Cas14u_CAS-V,WYL,csa3,DEDDh,cmr1gr7,cas10,cmr3gr5,cmr4gr7,cmr5gr11,cmr6gr7,PD-DExK,cas3,cas5,cas8c,cas7,cas4,cas1,cas2,DinG,cas14k	27	56	6	0

1. NZ_LN831776

CRISPR-Cas detection and classification

Crispr_ID: NZ_LN831776_1

• CRISPR_ID: NZ_LN831776_1
• CRISPR_location: 114326-114399
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: RT

Consensus repeat of NZ_LN831776_1

Consensus_repeat	Method
AATTAGTTACCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_1

>1.1|114349|28|NZ_LN831776|CRISPRCasFinder
AACCTGCGGAGAACAGGAGATTCGGGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_1

CRISPR arrays

The CRISPR arrays of NZ_LN831776_1

>merge|NZ_LN831776|1|114326-114399|CRISPRCasFinder
AATTAGTTACCCTTTTTCCACTTAACCTGCGGAGAACAGGAGATTCGGGCAAATTAGTTATCCTTTTTCCACTT

>NZ_LN831776|1|1|114326-114399|CRISPRCasFinder
AATTAGTTACCCTTTTTCCACTT	AACCTGCGGAGAACAGGAGATTCGGGCA
AATTAGTTATCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020425576.1|117137_117581_+|DUF1934-domain-containing-protein	unknown	unknown	gnl|CDD|378129
NZ_LN831776.1|WP_020425641.1|103448_104243_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425643.1|106404_106911_+|hypothetical-protein	unknown	unknown	gnl|CDD|378039
NZ_LN831776.1|WP_020425642.1|104287_106300_-|M1-family-metallopeptidase	unknown	unknown	gnl|CDD|341067
NZ_LN831776.1|WP_020428183.1|124106_124493_+|response-regulator	unknown	unknown	gnl|CDD|381105
NZ_LN831776.1|WP_046506230.1|102605_103034_-|C40-family-peptidase	unknown	unknown	gnl|CDD|366353
NZ_LN831776.1|WP_020428181.1|121354_121918_+|DNA-directed-RNA-polymerase-subunit-delta	unknown	unknown	gnl|CDD|275360
NZ_LN831776.1|WP_020425647.1|110852_112040_+|hypothetical-protein	unknown	unknown	gnl|CDD|372469
NZ_LN831776.1|WP_020425575.1|117577_119263_+|arginine--tRNA-ligase	unknown	unknown	gnl|CDD|234964
NZ_LN831776.1|WP_020428182.1|122191_123799_+|CTP-synthase	unknown	unknown	gnl|CDD|235437
NZ_LN831776.1|WP_020425644.1|107037_107511_-|hypothetical-protein	unknown	unknown	gnl|CDD|224913
NZ_LN831776.1|WP_020425579.1|114771_115629_+|carbon-nitrogen-hydrolase-family-protein	unknown	unknown	gnl|CDD|143598
NZ_LN831776.1|WP_020425639.1|101580_102072_-|C40-family-peptidase	unknown	unknown	gnl|CDD|366353
NZ_LN831776.1|WP_046500833.1|115644_116313_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831776.1|WP_046500837.1|119782_120952_-|S8-family-peptidase	unknown	unknown	gnl|CDD|173803
NZ_LN831776.1|WP_020425577.1|116355_117024_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425645.1|107748_108432_-|DNA-3-methyladenine-glycosylase	unknown	unknown	gnl|CDD|187726
NZ_LN831776.1|WP_020428184.1|124687_125542_+|class-II-fructose-1,6-bisphosphate-aldolase	unknown	unknown	gnl|CDD|181501
NZ_LN831776.1|WP_020425999.1|112670_113963_+|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	gnl|CDD|275209
NZ_LN831776.1|WP_020425646.1|108534_110607_-|PBP1A-family-penicillin-binding-protein	unknown	unknown	gnl|CDD|273955

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831776.1|WP_020425999.1|112670_113963_+|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	9.8e-52	170.3	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020425576.1|117137_117581_+|DUF1934-domain-containing-protein	gnl|CDD|378129	pfam09148, DUF1934, Domain of unknown function (DUF1934). Members of this family are found in a set of hypothetical bacterial proteins. Their precise function has not, as yet, been defined.	1.16923e-24
NZ_LN831776.1|WP_020425643.1|106404_106911_+|hypothetical-protein	gnl|CDD|378039	pfam08741, YwhD, YwhD family. This family of proteins are currently uncharacterized. They are around 170 amino acids in length.	3.97176e-94
NZ_LN831776.1|WP_020425642.1|104287_106300_-|M1-family-metallopeptidase	gnl|CDD|341067	cd09604, M1_APN_like, Peptidase M1 family similar to aminopeptidase N catalytic domain. This family contains bacterial M1 peptidases with smilarity to the catalytic domain of aminopeptidase N (APN; CD13; alanyl aminopeptidase; EC 3.4.11.2), a type II integral membrane protease belonging to the M1 gluzincin family. APN preferentially cleaves neutral amino acids from the N-terminus of oligopeptides and, in higher eukaryotes, is present in a variety of human tissues and cell types (leukocyte, fibroblast, endothelial and epithelial cells). APN expression is dysregulated in inflammatory diseases such as chronic pain, rheumatoid arthritis, multiple sclerosis, systemic sclerosis, systemic lupus erythematosus, polymyositis/dermatomyosytis and pulmonary sarcoidosis, and is enhanced in tumor cells such as melanoma, renal, prostate, pancreas, colon, gastric and thyroid cancers. It is predominantly expressed on stem cells and on cells of the granulocytic and monocytic lineages at distinct stages of differentiation, thus considered a marker of differentiation. Thus, APN inhibition may lead to the development of anti-cancer and anti-inflammatory drugs. APNs are also present in many pathogenic bacteria and represent potential drug targets. Some APNs have been used commercially, such as one from Lactococcus lactis used in the food industry. APN also serves as a receptor for coronaviruses, although the virus receptor interaction site seems to be distinct from the enzymatic site and aminopeptidase activity is not necessary for viral infection. APNs have also been extensively studied as putative Cry toxin receptors. Cry1 proteins are pore-forming toxins that bind to the midgut epithelial cell membrane of susceptible insect larvae, causing extensive damage. Several different toxins, including Cry1Aa, Cry1Ab, Cry1Ac, Cry1Ba, Cry1Ca and Cry1Fa, have been shown to bind to APNs; however, a direct role of APN in cytotoxicity has been yet to be firmly established.	7.09405e-150
NZ_LN831776.1|WP_020428183.1|124106_124493_+|response-regulator	gnl|CDD|381105	cd17553, REC_Spo0F-like, phosphoacceptor receiver (REC) domain of Spo0F and similar domains. Spo0F, a stand-alone response regulator containing only a REC domain with no output/effector domain, controls sporulation in Bacillus subtilis through the exchange of a phosphoryl group. Bacillus subtilis forms spores when conditions for growth become unfavorable. The initiation of sporulation is controlled by a phosphorelay (an expanded version of the two-component system) that consists of four main components: a histidine kinase (KinA), a secondary messenger (Spo0F), a phosphotransferase (Spo0B), and a transcription factor (Spo0A). REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	1.21587e-63
NZ_LN831776.1|WP_046506230.1|102605_103034_-|C40-family-peptidase	gnl|CDD|366353	pfam00877, NLPC_P60, NlpC/P60 family. The function of this domain is unknown. It is found in several lipoproteins.	1.98158e-38
NZ_LN831776.1|WP_020428181.1|121354_121918_+|DNA-directed-RNA-polymerase-subunit-delta	gnl|CDD|275360	TIGR04567, DNA-directed_RNA_polymerase_subunit_delta, DNA-directed RNA polymerase delta subunit. Members of this family are the RNA polymerase delta subunit, as found in the Firmicutes and the Mollicutes. All members of the seed alignment have an extended C-terminal low-complexity region, consisting largely of Asp and Glu, that is not included in the model. Proteins giving borderline scores should be checked to confirm a similar acidic C-terminal domain. [Transcription, DNA-dependent RNA polymerase].	1.03023e-31
NZ_LN831776.1|WP_020425647.1|110852_112040_+|hypothetical-protein	gnl|CDD|372469	pfam13088, BNR_2, BNR repeat-like domain. This family of proteins contains BNR-like repeats suggesting these proteins may act as sialidases.	1.53822e-05
NZ_LN831776.1|WP_020425575.1|117577_119263_+|arginine--tRNA-ligase	gnl|CDD|234964	PRK01611, argS, arginyl-tRNA synthetase; Reviewed.	0
NZ_LN831776.1|WP_020428182.1|122191_123799_+|CTP-synthase	gnl|CDD|235437	PRK05380, pyrG, CTP synthetase; Validated.	0
NZ_LN831776.1|WP_020425644.1|107037_107511_-|hypothetical-protein	gnl|CDD|224913	COG2002, AbrB, Regulators of stationary/sporulation gene expression [Transcription].	1.79281e-10
NZ_LN831776.1|WP_020425579.1|114771_115629_+|carbon-nitrogen-hydrolase-family-protein	gnl|CDD|143598	cd07574, nitrilase_Rim1_like, Uncharacterized subgroup of the nitrilase superfamily; some members of this subgroup have an N-terminal RimI domain (class 12 nitrilases). Some members of this subgroup are implicated in post-translational modification, as they contain an N-terminal GCN5-related N-acetyltransferase (GNAT) protein RimI family domain. The nitrilase superfamily is comprised of nitrile- or amide-hydrolyzing enzymes and amide-condensing enzymes, which depend on a Glu-Lys-Cys catalytic triad. This superfamily has been classified in the literature based on global and structure based sequence analysis into thirteen different enzyme classes (referred to as 1-13), this subgroup corresponds to class 12. Members of this superfamily generally form homomeric complexes, the basic building block of which is a homodimer.	1.42822e-141
NZ_LN831776.1|WP_020425639.1|101580_102072_-|C40-family-peptidase	gnl|CDD|366353	pfam00877, NLPC_P60, NlpC/P60 family. The function of this domain is unknown. It is found in several lipoproteins.	3.04325e-36
NZ_LN831776.1|WP_046500833.1|115644_116313_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	8.23775e-08
NZ_LN831776.1|WP_046500837.1|119782_120952_-|S8-family-peptidase	gnl|CDD|173803	cd07477, Peptidases_S8_Subtilisin_subset, Peptidase S8 family domain in Subtilisin proteins. This group is composed of many different subtilisins: Pro-TK-subtilisin, subtilisin Carlsberg, serine protease Pb92 subtilisin, and BPN subtilisins just to name a few. Pro-TK-subtilisin is a serine protease from the hyperthermophilic archaeon Thermococcus kodakaraensis and consists of a signal peptide, a propeptide, and a mature domain. TK-subtilisin is matured from pro-TK-subtilisin upon autoprocessing and degradation of the propeptide. Unlike other subtilisins though, the folding of the unprocessed form of pro-TK-subtilisin is induced by Ca2+ binding which is almost completed prior to autoprocessing. Ca2+ is required for activity unlike the bacterial subtilisins. The propeptide is not required for folding of the mature domain unlike the bacterial subtilases because of the stability produced from Ca2+ binding. Subtilisin Carlsberg is extremely similar in structure to subtilisin BPN'/Novo thought it has a 30% difference in amino acid sequence. The substrate binding regions are also similar and 2 possible Ca2+ binding sites have been identified recently. Subtilisin Carlsberg possesses the highest commercial importance as a proteolytic additive for detergents. Serine protease Pb92, the serine protease from the alkalophilic Bacillus strain PB92, also contains two calcium ions and the overall folding of the polypeptide chain closely resembles that of the subtilisins. Members of the peptidases S8 and S35 clan include endopeptidases, exopeptidases and also a tripeptidyl-peptidase. The S8 family has an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure and are not homologous to trypsin. The S53 family contains a catalytic triad Glu/Asp/Ser. The stability of these enzymes may be enhanced by calcium, some members have been shown to bind up to 4 ions via binding sites with different affinity. Some members of this clan contain disulfide bonds. These enzymes can be intra- and extracellular, some function at extreme temperatures and pH values.	1.26582e-99
NZ_LN831776.1|WP_020428184.1|124687_125542_+|class-II-fructose-1,6-bisphosphate-aldolase	gnl|CDD|181501	PRK08610, PRK08610, fructose-bisphosphate aldolase; Reviewed.	5.25773e-169
NZ_LN831776.1|WP_020425645.1|107748_108432_-|DNA-3-methyladenine-glycosylase	gnl|CDD|187726	cd00540, AAG, Alkyladenine DNA glycosylase catalyzes the first step in base excision repair. Alkyladenine DNA glycosylase (AAG), also known as 3-methyladenine DNA glycosylase, catalyzes the first step in base excision repair (BER) by cleaving damaged DNA bases within double-stranded DNA to produce an abasic site. AAG bends DNA by intercalating between the base pairs, causing the damaged base to flip out of the double helix and into the enzyme active site for cleavage. Although AAG represents one of six DNA glycosylase classes, it lacks the helix-hairpin-helix active site motif associated with other BER glycosylases and is structurally distinct from them.	5.69127e-88
NZ_LN831776.1|WP_020425999.1|112670_113963_+|group-II-intron-reverse-transcriptase/maturase	gnl|CDD|275209	TIGR04416, hypothetical_protein, group II intron reverse transcriptase/maturase. Members of this protein family are multifunctional proteins encoded in most examples of bacterial group II introns. These group II introns are mobile selfish genetic elements, often with multiple highly identical copies per genome. Member proteins have an N-terminal reverse transcriptase (RNA-directed DNA polymerase) domain (pfam00078) followed by an RNA-binding maturase domain (pfam08388). Some members of this family may have an additional C-terminal DNA endonuclease domain that this model does not cover. A region of the group II intron ribozyme structure should be detectable nearby on the genome by Rfam model RF00029. [Mobile and extrachromosomal element functions, Other].	0
NZ_LN831776.1|WP_020425646.1|108534_110607_-|PBP1A-family-penicillin-binding-protein	gnl|CDD|273955	TIGR02074, Includes:_Penicillin-insensitive_transglycosylase, penicillin-binding protein, 1A family. Bacterial that synthesize a cell wall of peptidoglycan (murein) generally have several transglycosylases and transpeptidases for the task. This family consists of bifunctional transglycosylase/transpeptidase penicillin-binding proteins (PBP). In the Proteobacteria, this family includes PBP 1A but not the paralogous PBP 1B (TIGR02071). This family also includes related proteins, often designated PBP 1A, from other bacterial lineages. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan].	0

Protein sequences

>NZ_LN831776.1|WP_020425999.1|112670_113963_+|group-II-intron-reverse-transcriptase/maturase
MNAKGLTTPKEKVQELQEKLGHAAKENKKRKFHALYDKVYRPDVLCEAWKRVKANKGAAGVDAVTLADIEERGETNFLKTCERELKEGSYHPQPVRRHYIPKKDGKPRPLGIPTVRDRVIQMATKLVIEPIFEADFEEVSFGFRPKRSAKGALERIRKACNRKGNWVVDVDIQGYFDNINQEKLMKLVQMRINDRRILKLIRKWLQAGVMEEGNVRRSDLGTPQGGVISPLLANIYLNYFDRLWEKHGSGLGELTRYADDFVVVCKTKKDAEHAYELISRIMERLELTLHPTKTRIVGLWTGDEGFDFLGMHHRKTKAETSQGKVYYTTQQWLTKKAEERIRGVVKERLAPPSMRSRTLAEQVEWLNPKIQGWRNYYYTNYSQKRLAKLDWYILQRLTRWYAKKRQRGRWMRSRSEVKYLTIQYGLKTLL
>NZ_LN831776.1|WP_020425647.1|110852_112040_+|hypothetical-protein
MNWTKKIYQGPLALLSAVLLAASAWGLSAPPAQAAAAQAAVPACSTGDHGLLKGLQAEHAASGTAPLNFSDIQFLNADTGRAAGNGFMIGTSDGGCHFQEIYKGQWSFRQIDFPDNVHGWALASVKGTAAAYLIATADGGSTWKRLTDTATVFDRIDFKDNKQGFGYSLASTYYTKDGGRTWRLIPTPANTRSAEFTSASSGYAVVVAPGAGYRIMKTSDGGATWSLSLKSAFAYPESGRVYANGDQVYALLYGGSGMSQTSYSLYASSNKGKSWSRVIAQNTAGGGPAPGNGAAQLTTGPASGKPGNMQLVGSSAAFLFGFSPAAEKVAVGRTYNGGKKWTNLPAIPGYDGLISFTGVTEGWMAVRGQNASSLYATEDGGSTWKLKFAFKGTEQ
>NZ_LN831776.1|WP_020425646.1|108534_110607_-|PBP1A-family-penicillin-binding-protein
MPREPVAPPKPKHRLRRLSRLLAVMGVLYVLAAGGLLGYLYHKDLPPIADDIRSKLLDSRGNVLTTFTTDGRSREPVTLNQISPLLIQATLAVEDRKFYKHSGFDVKGMGRAVLANLESGDRTQGASTLTQQLARNLYLSHEKTWTRKAKEALYTMQLEMKYSKDEILNMYLNQIYYGHGAYGIEAASQMYFGKAAADLDLAESAILAGIPKGPTYYSPYTHMDNAKKRQRIILAAMTEVGDITEAQATAARLETLSFKPQGEKNTLAAAPYFRDYVRSLATDTLHISSEELDQGGLNVYTTLDPDMQQAAEDAVEKGMDPSGDLETALVSIDPRTGYIKAMVGGKNYRTNQFNHALATTRQPGSSFKPIMYLTALSSKSMTGLSVFNSQPTLFHYDNDRKTYQPKNFGDKYLGEINMRQAIAASDNIYAVNTIMKVGADKVADMAAKMGIDSPLQTVPSLALGTSPVSPLEMASAFAVIGGGGVKLPVTAILKITDANGKLLYEAPQTQGEKVVEPAAAYVLTRLMEGVFESGGTGNRVASMIKRPVAGKTGTTDTDGWMVGFTPELSTAVWVGYDKGRDIATADGRRAAPIFAQFTEKALENVPPKIFPIPDGVVSVYVNPQSGKLATAACPEKVLETFISGTEPKEYCDQHGAGGAVSPPDGSGEPPAEDIKEEHSLWKDIKRWWLN
>NZ_LN831776.1|WP_020425645.1|107748_108432_-|DNA-3-methyladenine-glycosylase
MNLKNNSDGREGPPSRNLLSPDLYKLTALQAGPLLLGQHLVRRTEDGEIRCRIVETESYGGAEDKGSHAYGGRRTARTEVMFSAGGTAYVYLIYGMYHCVNVVTAAEHDPHAVLIRAVEPLTSTDAARMAAYRGITVKKPSSLSGGPGKLCRALRIDKSLNGCRLDDPLGPLWLEQGDSPEHLDIAAAPRINIPYAEEYAPLPWRFYLRGNPYVSVIDKQAEPFSLS
>NZ_LN831776.1|WP_020425644.1|107037_107511_-|hypothetical-protein
MKDTGMIRSLDSLGRIVVPVEIRMTRNIDIGDPIEFFILDEEIIVLRKYTSTECTFCRSLDHVSYYKDQFICNSCLKELGNPDRTADEAVQLQSPAEITPEPGRGGRRSKTEEMSQRLEKAIEDHPYANQKELAEVLGISQARVSQLKRKLNLLSRS
>NZ_LN831776.1|WP_020425643.1|106404_106911_+|hypothetical-protein
MDNNQPEGKKPMALNIVNAKSKHKGFGAGSIDLNNVSPVIIDGGEAVIDIGAMHAKSKVEKGIKFSPNREDVPNGRQVWVVWVAVDRTPEGQSYGGVTACEMWIDTEARRGWKILADHVNKLDSALKRRVILEGLGAADKAALKALLIAHNAEWWDASTAELKAALSE
>NZ_LN831776.1|WP_020425642.1|104287_106300_-|M1-family-metallopeptidase
MKPLSFRYTLIFAALATLALLGGGIWALSGHNPAVQTAAAPKEAKSPAAVQIKAPQPVLPESRPLPVSEALSQRVTEYHLEAQLLPSTGSLTASETVTWTHPGRKPVQDLYFHLYPNAFASKDTTFMKESGGKLRGDTMPANGYGSMTLTDLRTSDGISLMQRLQYVQPDDGNVHDKTLVKVHLPQPVNGGESVTLKLKFTVALPKIFARMGVSGNFIMAGQWFPKISVYEPAGTRGVKQEGWNLHQYHGTSEFYSDFGIYNVTLSVPSNYTVAATGFPVKTAKLKQGQKIYKFYADDVHDFAWAASPDFLVAEEAFSSSEVPGVRIKLYLDPLHKDLQERYFQAAKAALNTFSKWYGPYPYSTLSIVVPPKEGSGAGGMEYPTLVTASSASENVPGTQLERTIIHEIGHQFFYGMVASNEFEEAWLDESFTSYAEDRLMEQEYGVASNLPLQASLVPSAQPLTLETWKYTGDDAYTRNIYIRGKLVLKDIEHQVGTKTMDAILAAYARKYRFRHPSTADFQRTVEKVTKKSWQTYFDHYVYSGGAPDFAINHIANTISKAGADNEDSRYESSVNVSNKGSWYGDVPVKFTFSDGYTVQRYWNGESKQTTFQLSYKAPLLSAEIDPEHSVLLESKHLNNFRLAELEPDTLSRWTLSMTNLIENLLGTLVW
>NZ_LN831776.1|WP_020425641.1|103448_104243_-|hypothetical-protein
MKEQLYILILLFIYRLFWGYFMYKFVKSAVVPVLLRYPDQHAGGSGLGRLLYYVEGQFALGSDPAVQHWLWMLLALSAARLLVSPFIRAGLLHELHQERKGERGMFFFPGMRLYGLPVMLFSLIEWVLAALPLYWLFPKMYNLLLSGILDYRQLLKLVPYVLAWLVYLFFIRKLLLYMQFGYTAGTGILPSLLVCLKVIVPSVGLSLVLGACGLVMMLICGATALLSPGLPAFLLRQFSPLPTTLFKMWGIAAQYHLWRSKTFP
>NZ_LN831776.1|WP_046506230.1|102605_103034_-|C40-family-peptidase
MVFTFGAGSAFADSKMDTVIAKTIGTTYKFGGTSTSGFDCSGFTRYVFKNVGLTLPRTSKAQFSVGTPVSRNNLRSGDLVFFNTFGSGVSHVGIYVGNGKFAQSSSSRGVTITSLSQAYWANRYVGAKRVMSTTAYQAVAYD
>NZ_LN831776.1|WP_020425639.1|101580_102072_-|C40-family-peptidase
MKKKLASALLSFSIILTIGAGSAFADSKMDQVIDKAIGTRYVSGGISTNGFDCSGFTMYVFDKIGINLPHQSGSQYQMGTAISRDNIRPGDLVFFNTSGNGVSHVGIYVGEGKFAHASSKRGVTVSSLNDSYYVNRYVGAKRIMSTDAYQNVASDSQDNDDVQ
>NZ_LN831776.1|WP_020425579.1|114771_115629_+|carbon-nitrogen-hydrolase-family-protein
MAFRVSAVQYHLHTISSFGEFAAECEHYIKTAGEYGAEFILFPEFLTTQLMSIGDEQGKALTIEDLPQFTDRYRELFAGYAQKYAVHIIGGTHVLRRNGKLYNVAHLFYPDGRIAEQAKLHITPAEVEGWNMGAGEGLEVFQTDKGTIAMLTCYDIEFPEIVRMARAKGADVIFCPSCTDDRHGFHRVRYTSHARAVENQVYVVLTGTVGSLPTVDLMRANFGQAAVITPNDIPFPPQGLLAEGEINSDMIITADLDLELLYRVRERGSVTTWRDRRTDLYTDWT
>NZ_LN831776.1|WP_046500833.1|115644_116313_+|GNAT-family-N-acetyltransferase
MYYKSFYAFDGKIPVPAVIRSYTEADFTELITIQSEAFPPPYPAELWWNREQLLNHVTLFPEGALCVEVNGELAGSVTGLKIRFDPKAPALQHTWSEVTADGYITTHQPDGNTLYIADLCVRPKYRKLGLGKELVQSLYHAVVEQKLERLLGAGRMPGYHLQASRMSAEEYLAGVVAGKWSDPVITFLLRCGRSPVGVVADYLEDEESGNYAALMEWRNPFL
>NZ_LN831776.1|WP_020425577.1|116355_117024_+|hypothetical-protein
MEYSRITSVADPLFRQVHNLLSEVFPPEEVLEYSLWKEPLEDPGIRVFAAVHEGSVVGTTEYRYYSDWNVAMTDFTIIGREGLGVGRFLAQHRLKDLQKLAADNGKELFGMFAEIYDPYRVEHAFGGIKPMDPFVRREVLSHLGYKRLDFPYVHPSWQGDGEAVAGLDLCFMPGDENLEQIEAALVAGFLTRYYAVLADKPEAWTSMVEQLKGRDAVSLLPL
>NZ_LN831776.1|WP_020425576.1|117137_117581_+|DUF1934-domain-containing-protein
MTESESDKYGVSVTLESVQGGERNVVRAAGEVITRGNQLYLRYEETQPGPKDEAVSVRTTVKITDNGLKLIRHGGVQSEQSFEPGQRLPGFYRSPYTQFNLSTDTRKLDVKRAGKSLAVAWEYDLYVYGELSGQFAISLHIQEEPQS
>NZ_LN831776.1|WP_020425575.1|117577_119263_+|arginine--tRNA-ligase
MTQSQNPLRLANERLREAVAGAIIAAGLVTREELPAIVLEVPKDKAHGDLATNAAMQLTKIAKRNPRQIAEAIIGHLDKNAASIEKAEIAGPGFINFTLSKSYLYPVIALVAEQGDNYGRIDAGQGQRVEMEFVSANPTGSLHLGHARGAAVGDALCNVLDFAGYEVTREYYINDAGNQVANLCKSIEARYLQELGQPAEMPEDGYHGEDIKGFAKELVAEKGDALLSMTPGDRAAFFRTYGLTKELDKIKRDLTRFRVGFDIWFSETSLYENGEVLRSLDELRERGEVYEQDGATWLQTTKYGDDKDRVLIKNDGTYTYLTPDIAYHNDKYGRGYDTMINIWGADHHGYIPRMKAAMSALGNDPEKLVVLIAQMVSLFQNGEKVKMSKRTGKAVTMEDLMDEVGIDAIRYFFTMRSMDSHLDFDMDLAISTSNENPVFYVQYAHARICSIFRQAEEQGIVLPDVAEIDYAKLTAEHEYALLRKIGELPAEIGIAASSYAPHRLIRYVYDLASLFHSYYKAERVITEDAAQTLARLALLGAARTTIANVLRLVGVTAPDRM
>NZ_LN831776.1|WP_046500837.1|119782_120952_-|S8-family-peptidase
MDYYRFWQILLNEISAAPKNADRRIVTFKDARQYAGALSEWKSLKAKTPGLRRVQMSPLIRAFFVPAAGAGKLLQTFEDALCIEEDARIQVHAAAPEKSGASLMPWGVKAIHAPQAWSRSTGVHVKIGVIDTGADYRHPDLKHSLASGVNLLYRGMLPFDDNGHGTHIAGTLAAAGGTRGMMGVAPRAQLYPVKAFDHNGSAYVSDIVLGIDWCVQNRIDIINMSFGMKTRSKALHDVVIKAYRAGIAIIASSGNDGKRGGDYPARYPETIAVGALDRRHRVAAFSNRGPYIDVYGPGESVTSCWLKEGYKEMSGTSMATSHVTGAAALLLALRPGLSPRELKLLLRRTASPVRLRKGQRRAALGGGAADALRLLRAGARAKRAAAAKA
>NZ_LN831776.1|WP_020428181.1|121354_121918_+|DNA-directed-RNA-polymerase-subunit-delta
MSTPLNLKLDPEKVKEMPMVDLAFLVLKAANTPYYYRDLMVEVAKLRGMTEEQTNDTIAQLYTEINIDGRFACVGTNLWGLKRWYPLERSDDPVGNSKRPRIINDEDDDLEDDDFAEEEDNYAAEEEDFDAIDEDRDDLYSDDDSEEEVDEDVVIDEDDIDEDDVDDEDSEDGDDEDADDEDENDNY
>NZ_LN831776.1|WP_020428182.1|122191_123799_+|CTP-synthase
MTKYIFVTGGVVSSLGKGITAASLGRLLKNRGLKVTIQKFDPYINVDPGTMSPYQHGEVFVTDDGAETDLDLGHYERFIDINLSKNSNVTTGKIYSSVISKERRGEYLGGTVQVIPHITNEIKERVFRAGRETGSDVVITEIGGTVGDIESLPFLEAIRQIKSDIGRENVMYIHVTLIPYIKAAGEVKTKPTQHSVKELRSIGIQPNVIVCRTEYALSDDMKAKIALFCDIDANAVVECRDASTLYEVPLNLRDEGLDEIVVNHLKLTTPAPDMREWENMLGRIQKLERTVEIAIVGKYVALHDAYLSVVESLSHAGFAANAEVKVRWVDAELVTDENVGELLGGIGGILVPGGFGDRGIEGKISAIRYAREQSIPFFGICLGMQVSVIEYGRSILGLAGANSSEIDPATLHPLIDLLPEQKDIEDMGGTMRLGLYPCKLLPESLAMSCYDDELVYERHRHRYEFNNAYRDEIEKAGLVISGTSPDGRLVEIVELPGHPWFLSVQFHPEFTSRPNRPQPLFREFVKASLTHSEQL
>NZ_LN831776.1|WP_020428183.1|124106_124493_+|response-regulator
MEKKKVLIVDDQNGIRILLMEVFNSEGYATFQAANGKLALDIVRSESPDLVLLDMKIPGMDGLEILKHLKEINPAIKVIMMTAYGELDMIKEATKLGALMHFTKPFDIDEMRIAVNMHLNNKSIDQCS
>NZ_LN831776.1|WP_020428184.1|124687_125542_+|class-II-fructose-1,6-bisphosphate-aldolase
MPLVSMTDMLNKALQGKYAVGQYNINNLEWTQAILGAAEEEKSPVILGVSEGAARHMGGFYTVVKMVEGLIHDMKITVPVAIHLDHGSSFDKCKEAIDAGFTSVMIDGSHHPIDENIEMTKKVVDYAHAKGVSVEAEVGTVGGQEDDVIGGIQYADLNECVRIVKETGIDTLAPALGSVHGPYHGEPNLGFKEMEEIRDAVKLPLVLHGGTGIPEHDIKKSISLGTSKINVNTENQIAFAKVVREVLAAKPDAYDPRTFIAPGREAIKQTVIGKIREFGSSNKA

Crispr_ID: NZ_LN831776_2

• CRISPR_ID: NZ_LN831776_2
• CRISPR_location: 134095-134169
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: RT

Consensus repeat of NZ_LN831776_2

Consensus_repeat	Method
AATTAGTGTCCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_2

>2.1|134118|29|NZ_LN831776|CRISPRCasFinder
CATCTGCCCGAGGATAGGGTACTCCGGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_2

CRISPR arrays

The CRISPR arrays of NZ_LN831776_2

>merge|NZ_LN831776|2|134095-134169|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTTCATCTGCCCGAGGATAGGGTACTCCGGCAAATTAGTGTCCCTTTTTCCACTT

>NZ_LN831776|2|2|134095-134169|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTT	CATCTGCCCGAGGATAGGGTACTCCGGCA
AATTAGTGTCCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020425530.1|147733_148672_+|HPr-kinase/phosphorylase	unknown	unknown	gnl|CDD|235459
NZ_LN831776.1|WP_082118058.1|143283_144684_+|hypothetical-protein	unknown	unknown	gnl|CDD|377437
NZ_LN831776.1|WP_020426415.1|132597_132909_+|YbaB/EbfC-family-nucleoid-associated-protein	unknown	unknown	gnl|CDD|234669
NZ_LN831776.1|WP_020428182.1|122191_123799_+|CTP-synthase	unknown	unknown	gnl|CDD|235437
NZ_LN831776.1|WP_020425531.1|148684_149716_+|prolipoprotein-diacylglyceryl-transferase	unknown	unknown	gnl|CDD|183527
NZ_LN831776.1|WP_020425532.1|149723_150377_+|pyrophosphatase-PpaX	unknown	unknown	gnl|CDD|237336
NZ_LN831776.1|WP_020426332.1|134718_134985_+|hypothetical-protein	unknown	unknown	gnl|CDD|377835
NZ_LN831776.1|WP_020428183.1|124106_124493_+|response-regulator	unknown	unknown	gnl|CDD|381105
NZ_LN831776.1|WP_020426412.1|128662_129940_+|radical-SAM-protein	unknown	unknown	gnl|CDD|100105
NZ_LN831776.1|WP_020425533.1|150373_150898_+|acyltransferase	unknown	unknown	gnl|CDD|100053
NZ_LN831776.1|WP_020428184.1|124687_125542_+|class-II-fructose-1,6-bisphosphate-aldolase	unknown	unknown	gnl|CDD|181501
NZ_LN831776.1|WP_020426416.1|132945_133545_+|recombination-protein-RecR	unknown	unknown	gnl|CDD|234616
NZ_LN831776.1|WP_020425999.1|141953_143246_+|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	gnl|CDD|275209
NZ_LN831776.1|WP_020426333.1|134438_134687_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426413.1|130059_130257_+|50S-ribosomal-protein-L31	unknown	unknown	gnl|CDD|376487
NZ_LN831776.1|WP_025709140.1|146279_147401_+|sn-glycerol-3-phosphate-ABC-transporter-ATP-binding-protein-UgpC	unknown	unknown	gnl|CDD|236947
NZ_LN831776.1|WP_020428185.1|125857_127111_+|UDP-N-acetylglucosamine-1-carboxyvinyltransferase	unknown	unknown	gnl|CDD|183779
NZ_LN831776.1|WP_020426414.1|130775_132551_+|DNA-polymerase-III-subunit-gamma/tau	unknown	unknown	gnl|CDD|235505
NZ_LN831776.1|WP_046500839.1|127279_128638_+|transcription-termination-factor-Rho	unknown	unknown	gnl|CDD|236490
NZ_LN831776.1|WP_020426165.1|145075_146170_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|379258

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831776.1|WP_020425999.1|141953_143246_+|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	9.8e-52	170.3	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_082118058.1|143283_144684_+|hypothetical-protein	gnl|CDD|377437	pfam04986, Y2_Tnp, Putative transposase. Transposases are needed for efficient transposition of the insertion sequence or transposon DNA. This family includes transposases IS1294 and IS801. This is a rolling-circle transposase.	1.43425e-38
NZ_LN831776.1|WP_025709140.1|146279_147401_+|sn-glycerol-3-phosphate-ABC-transporter-ATP-binding-protein-UgpC	gnl|CDD|236947	PRK11650, ugpC, sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC.	8.93183e-180
NZ_LN831776.1|WP_020428182.1|122191_123799_+|CTP-synthase	gnl|CDD|235437	PRK05380, pyrG, CTP synthetase; Validated.	0
NZ_LN831776.1|WP_020425531.1|148684_149716_+|prolipoprotein-diacylglyceryl-transferase	gnl|CDD|183527	PRK12437, PRK12437, prolipoprotein diacylglyceryl transferase; Reviewed.	6.07072e-103
NZ_LN831776.1|WP_020425532.1|149723_150377_+|pyrophosphatase-PpaX	gnl|CDD|237336	PRK13288, PRK13288, pyrophosphatase PpaX; Provisional.	2.06881e-81
NZ_LN831776.1|WP_020426332.1|134718_134985_+|hypothetical-protein	gnl|CDD|377835	pfam07441, BofA, SigmaK-factor processing regulatory protein BofA. This family contains the sigmaK-factor processing regulatory protein BofA (Bypass-of-forespore protein A) (approximately 80 residues long). During sporulation in Bacillus subtilis, transcription is controlled in the developing sporangium by a cascade of sporulation-specific transcription factors (sigma factors). Following engulfment, processing of sigmaK is inhibited by BofA. It has been suggested that this effect is exerted by alteration of the level of the SpoIVFA protein.	0.00198006
NZ_LN831776.1|WP_020428183.1|124106_124493_+|response-regulator	gnl|CDD|381105	cd17553, REC_Spo0F-like, phosphoacceptor receiver (REC) domain of Spo0F and similar domains. Spo0F, a stand-alone response regulator containing only a REC domain with no output/effector domain, controls sporulation in Bacillus subtilis through the exchange of a phosphoryl group. Bacillus subtilis forms spores when conditions for growth become unfavorable. The initiation of sporulation is controlled by a phosphorelay (an expanded version of the two-component system) that consists of four main components: a histidine kinase (KinA), a secondary messenger (Spo0F), a phosphotransferase (Spo0B), and a transcription factor (Spo0A). REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	1.21587e-63
NZ_LN831776.1|WP_020426412.1|128662_129940_+|radical-SAM-protein	gnl|CDD|100105	cd01335, Radical_SAM, Radical SAM superfamily. Enzymes of this family generate radicals by combining a 4Fe-4S cluster and S-adenosylmethionine (SAM) in close proximity. They are characterized by a conserved CxxxCxxC motif, which coordinates the conserved iron-sulfur cluster. Mechanistically, they share the transfer of a single electron from the iron-sulfur cluster to SAM, which leads to its reductive cleavage to methionine and a 5'-deoxyadenosyl radical, which, in turn, abstracts a hydrogen from the appropriately positioned carbon atom. Depending on the enzyme, SAM is consumed during this process or it is restored and reused. Radical SAM enzymes catalyze steps in metabolism, DNA repair, the biosynthesis of vitamins and coenzymes, and the biosynthesis of many antibiotics. Examples are biotin synthase (BioB), lipoyl synthase (LipA), pyruvate formate-lyase (PFL), coproporphyrinogen oxidase (HemN), lysine 2,3-aminomutase (LAM), anaerobic ribonucleotide reductase (ARR), and MoaA, an enzyme of the biosynthesis of molybdopterin.	9.21946e-12
NZ_LN831776.1|WP_020425533.1|150373_150898_+|acyltransferase	gnl|CDD|100053	cd04647, LbH_MAT_like, Maltose O-acyltransferase (MAT)-like: This family is composed of maltose O-acetyltransferase, galactoside O-acetyltransferase (GAT), xenobiotic acyltransferase (XAT) and similar proteins. MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively while GAT specifically acetylates galactopyranosides. XAT catalyzes the CoA-dependent acetylation of a variety of hydroxyl-bearing acceptors such as chloramphenicol and streptogramin, among others. XATs are implicated in inactivating xenobiotics leading to xenobiotic resistance in patients. Members of this family contain a a left-handed parallel beta-helix (LbH) domain with at least 5 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X). They are trimeric in their active form.	2.07236e-28
NZ_LN831776.1|WP_020428184.1|124687_125542_+|class-II-fructose-1,6-bisphosphate-aldolase	gnl|CDD|181501	PRK08610, PRK08610, fructose-bisphosphate aldolase; Reviewed.	5.25773e-169
NZ_LN831776.1|WP_020426416.1|132945_133545_+|recombination-protein-RecR	gnl|CDD|234616	PRK00076, recR, recombination protein RecR; Reviewed.	1.35097e-125
NZ_LN831776.1|WP_020425999.1|141953_143246_+|group-II-intron-reverse-transcriptase/maturase	gnl|CDD|275209	TIGR04416, hypothetical_protein, group II intron reverse transcriptase/maturase. Members of this protein family are multifunctional proteins encoded in most examples of bacterial group II introns. These group II introns are mobile selfish genetic elements, often with multiple highly identical copies per genome. Member proteins have an N-terminal reverse transcriptase (RNA-directed DNA polymerase) domain (pfam00078) followed by an RNA-binding maturase domain (pfam08388). Some members of this family may have an additional C-terminal DNA endonuclease domain that this model does not cover. A region of the group II intron ribozyme structure should be detectable nearby on the genome by Rfam model RF00029. [Mobile and extrachromosomal element functions, Other].	0
NZ_LN831776.1|WP_020426415.1|132597_132909_+|YbaB/EbfC-family-nucleoid-associated-protein	gnl|CDD|234669	PRK00153, PRK00153, YbaB/EbfC family nucleoid-associated protein.	3.75454e-43
NZ_LN831776.1|WP_020426413.1|130059_130257_+|50S-ribosomal-protein-L31	gnl|CDD|376487	pfam01197, Ribosomal_L31, Ribosomal protein L31.	1.97216e-34
NZ_LN831776.1|WP_020425530.1|147733_148672_+|HPr-kinase/phosphorylase	gnl|CDD|235459	PRK05428, PRK05428, HPr kinase/phosphorylase; Provisional.	8.29272e-171
NZ_LN831776.1|WP_020428185.1|125857_127111_+|UDP-N-acetylglucosamine-1-carboxyvinyltransferase	gnl|CDD|183779	PRK12830, PRK12830, UDP-N-acetylglucosamine 1-carboxyvinyltransferase; Reviewed.	0
NZ_LN831776.1|WP_020426414.1|130775_132551_+|DNA-polymerase-III-subunit-gamma/tau	gnl|CDD|235505	PRK05563, PRK05563, DNA polymerase III subunits gamma and tau; Validated.	0
NZ_LN831776.1|WP_046500839.1|127279_128638_+|transcription-termination-factor-Rho	gnl|CDD|236490	PRK09376, rho, transcription termination factor Rho; Provisional.	0
NZ_LN831776.1|WP_020426165.1|145075_146170_+|helix-turn-helix-domain-containing-protein	gnl|CDD|379258	pfam13556, HTH_30, PucR C-terminal helix-turn-helix domain. This helix-turn-helix domain is often found at the C-terminus of PucR-like transcriptional regulators such as Bacillus subtilis pucR and is likely to be DNA-binding.	1.28232e-17

Protein sequences

>NZ_LN831776.1|WP_020426416.1|132945_133545_+|recombination-protein-RecR
MYYPEPLAKLIEAFTRLPGIGPKSATRLAFHVLNMKEDEVIDFAKALVSVKRNLHYCSVCCNITDTDPCRICQDKTRDASVICVVQDSKDLVAIERTKEFDGYYHVLQGAISPMEGIGPDDIRLKELLTRLSDERVKELIMATNPNIEGEATAMYISRLVRPFEIKITRIAHGLPVGGDLEYADEVTLSKALEGRRELF
>NZ_LN831776.1|WP_020426415.1|132597_132909_+|YbaB/EbfC-family-nucleoid-associated-protein
MNNMNQMMKQVKKMQEQMLKAQEELGSKTIEGSSGGGVVTVQVNGHKKLLSIQIKPEAVDPDDIEMLQDLVITAVNDALTQAEELANNDMGKFTGGMKIPGLF
>NZ_LN831776.1|WP_020426414.1|130775_132551_+|DNA-polymerase-III-subunit-gamma/tau
MEHIALYRAWRPQSFHDMVGQQHIIQTLQNAIREQRVSHAYLFSGPRGTGKTSAAKVLAKAVNCERSEGAEPCNECPSCLRITAGNVMDVQEIDAASNRGVEEIRDLRDKVKYAPTEVRRKVYIIDEVHMLTTEAFNALLKTLEEPPPHVMFILATTEPHKLPATIISRCQRFDFRRVSLEEQTAHLTAICQKEGISADSDALQYIARLSDGGMRDALSILDQISSFTDGQVTYQQVLGMTGGIPSEQFARLATAILEGDMGLLLELVEQLMHEGKSADKCLENLLYYFRDLLMIKMVPGADQLTDRVLNPADFRDMAAAFTRDRLFLIVETLTRYLGEMKYATHPQTLFEVALMKLCSLQQQEGSPHGTTPQAASSHVVGGNAAAVDSGELEHLKRQIAALEKKLEQAMQSGAMSGGGRGEQGNQGRQPAQAPAPRVSSPSKLPPQLDKFIAGKDSPDFAEVYKKWSVVLQGVKEEKVTVHAWFVDGEPVAVMEDAVLVAFKNTIHRDTTEKPANRQVIENVFAARLGKPYRLVTMMLRDWNEAATKTAAQTSTEELQLEHEHETGDTRTEPWIDEAIQLFGEDLVVIKE
>NZ_LN831776.1|WP_020426413.1|130059_130257_+|50S-ribosomal-protein-L31
MQSAIQPKYNVTKVTCACGNTFETGSVKAELRVEICSSCHPFFTGKQKFMDAGGRVDKFKKKYGI
>NZ_LN831776.1|WP_020426412.1|128662_129940_+|radical-SAM-protein
MYLVYADEQGNVYDHSELYGLARSGDMIVEMLEEELIPLPEGATLVGLPNTRAVGMNPKTGEMLPLPEGSQAVGALLPQGFTRLCLPGYVKTDKSYKLPLFGYSAVVWKDGGFYVAADLTDDPEQWNPLNCDREDVEAGVGSLTAKYPGNRLYGHLSNCALGYECLTSSNTFLGRWEGAVPVSYSCNAGCFGCISEQPDDSGFVSPQTRMNFRPTVNEISEVMLEHLKTPQSIISFGQGCEGEPSTQAKLIIEAIREVRSITDMGYININTNAGLSDHIRGIVDAGLDLMRVSTISALDDHYNAYYKPRGYTLANVEKSLKYAASQGVYTSINYLIFPGVTDREEEIEAMVEFVRRTDLKLIQMRNLNIDPESYLELIPPAQGEILGMKTMLEIFREELPDVVIGSYTHVPPADLARAKQRRVKI
>NZ_LN831776.1|WP_046500839.1|127279_128638_+|transcription-termination-factor-Rho
MDLQISDLEEMKLTDLYKLAKKYQIPYYGTLKKRELIFAILRAQAEQSGLMFMEGVLEILPEGYGFLRPINYLPSAEDIYISASQIRKFDLRSGDLVSGKCRTPKENERYFGLLQVNAVNGENPASAAERLHFPALTPLYPQDKLPLETSPTQLSTRIMDLLAPVGLGQRGLIVAPPKAGKTLLLKEIANSISTNNPEIALFVLLIDERPEEVTDMQRSVKGEVVASTFDELPENHIKVAELVLQRALRLVEHKKDVVILLDSITRLARAYNLVVPPSGRTLSGGIDPAAFHRPKRFFGSARNVEEGGSLTILATALIDTGSRMDDIIYEEFKGTGNMELHLDRKLAERRIFPAIDIRRSGTRREEVLLSKEELDTIWAIRKNMNESYDFVEGFLKKLRDSKTNAEFLASFDVAGNKESSSPSGTASNGGTSNSGSSARRTSRPKTPSVPTT
>NZ_LN831776.1|WP_020428185.1|125857_127111_+|UDP-N-acetylglucosamine-1-carboxyvinyltransferase
MEKLMIGGGRPLEGVVTISGAKNSAIALIPAAILAESEVVLDNLPSLSDVAVYSEILEELGATVSWTGSQMRINPSRIVSIPMPNGPVKKLRASYYMMGALLGRFKEATIGLPGGCNFEPRPIDQHIKGFEALGATVTNDHGSIHLYAKELRGAKIYLDVSSVGATINIMLAASRAKGSTIIENAAKEPEIIDVATLLNSMGAVIKGAGTETIRIEGVTEMHGCRHSIIPDRIQAGTYMIAAAATRGNVLIDNVIPKHLEALTAKLLEMGVNIEELDESIRVIGQGKYEHADVKALIYPGFATDLQSPMTSMLTQAEGVSVLSDFVYSNRFKHVPELVRMGAKIRVEGRSAIIEGSRLNAAKVKAADLRAGAALVIAGLTVEEGITEVTGVEFIDRGYDNLVSNLRNLGADVWRENE
>NZ_LN831776.1|WP_020428184.1|124687_125542_+|class-II-fructose-1,6-bisphosphate-aldolase
MPLVSMTDMLNKALQGKYAVGQYNINNLEWTQAILGAAEEEKSPVILGVSEGAARHMGGFYTVVKMVEGLIHDMKITVPVAIHLDHGSSFDKCKEAIDAGFTSVMIDGSHHPIDENIEMTKKVVDYAHAKGVSVEAEVGTVGGQEDDVIGGIQYADLNECVRIVKETGIDTLAPALGSVHGPYHGEPNLGFKEMEEIRDAVKLPLVLHGGTGIPEHDIKKSISLGTSKINVNTENQIAFAKVVREVLAAKPDAYDPRTFIAPGREAIKQTVIGKIREFGSSNKA
>NZ_LN831776.1|WP_020428183.1|124106_124493_+|response-regulator
MEKKKVLIVDDQNGIRILLMEVFNSEGYATFQAANGKLALDIVRSESPDLVLLDMKIPGMDGLEILKHLKEINPAIKVIMMTAYGELDMIKEATKLGALMHFTKPFDIDEMRIAVNMHLNNKSIDQCS
>NZ_LN831776.1|WP_020428182.1|122191_123799_+|CTP-synthase
MTKYIFVTGGVVSSLGKGITAASLGRLLKNRGLKVTIQKFDPYINVDPGTMSPYQHGEVFVTDDGAETDLDLGHYERFIDINLSKNSNVTTGKIYSSVISKERRGEYLGGTVQVIPHITNEIKERVFRAGRETGSDVVITEIGGTVGDIESLPFLEAIRQIKSDIGRENVMYIHVTLIPYIKAAGEVKTKPTQHSVKELRSIGIQPNVIVCRTEYALSDDMKAKIALFCDIDANAVVECRDASTLYEVPLNLRDEGLDEIVVNHLKLTTPAPDMREWENMLGRIQKLERTVEIAIVGKYVALHDAYLSVVESLSHAGFAANAEVKVRWVDAELVTDENVGELLGGIGGILVPGGFGDRGIEGKISAIRYAREQSIPFFGICLGMQVSVIEYGRSILGLAGANSSEIDPATLHPLIDLLPEQKDIEDMGGTMRLGLYPCKLLPESLAMSCYDDELVYERHRHRYEFNNAYRDEIEKAGLVISGTSPDGRLVEIVELPGHPWFLSVQFHPEFTSRPNRPQPLFREFVKASLTHSEQL
>NZ_LN831776.1|WP_020426333.1|134438_134687_+|hypothetical-protein
MGWWSIRRQADGEQKRIDDDHWNVFLEVQQAHSEWERAYLMFDEAKGQDQIDYAIYILEAAERKYQIHLKHAKSLGLNRAQL
>NZ_LN831776.1|WP_020426332.1|134718_134985_+|hypothetical-protein
MLRMAALAVLVLSGLLLLLIVFKKKLGWAWLSLFGTHLLLAALGIYIVNFSGLLTDIYIPLNPATIGAVTVLGLPGVLMLMGLKLTLF
>NZ_LN831776.1|WP_020425999.1|141953_143246_+|group-II-intron-reverse-transcriptase/maturase
MNAKGLTTPKEKVQELQEKLGHAAKENKKRKFHALYDKVYRPDVLCEAWKRVKANKGAAGVDAVTLADIEERGETNFLKTCERELKEGSYHPQPVRRHYIPKKDGKPRPLGIPTVRDRVIQMATKLVIEPIFEADFEEVSFGFRPKRSAKGALERIRKACNRKGNWVVDVDIQGYFDNINQEKLMKLVQMRINDRRILKLIRKWLQAGVMEEGNVRRSDLGTPQGGVISPLLANIYLNYFDRLWEKHGSGLGELTRYADDFVVVCKTKKDAEHAYELISRIMERLELTLHPTKTRIVGLWTGDEGFDFLGMHHRKTKAETSQGKVYYTTQQWLTKKAEERIRGVVKERLAPPSMRSRTLAEQVEWLNPKIQGWRNYYYTNYSQKRLAKLDWYILQRLTRWYAKKRQRGRWMRSRSEVKYLTIQYGLKTLL
>NZ_LN831776.1|WP_082118058.1|143283_144684_+|hypothetical-protein
MRENLTYGLMRRGWVAPALYSEIMQCKKMWITPMKKVGGMNVKNQETWKKRGIIRQILKDHFHGFMEMHGHHLPKGLHSSITETVNKAIRCGTRDMGYARYECKGCTKGAPEPVFICFTCKSRFCHGCGKKYTDEWAEKQQERILNVPHRHMVFTVPQELRKVFFQDRHKLNELSKQVAKVIQYYYRRKNKSKKYEVGVITVIHTFGRDLKFNPHIHTLITEGALEQNKEWKKVEYISYEYLRKAWQKLLLDLMMKWYPKEEWIKGLVNELYQRYPQGFYVNAEQRMKDARGAAKYIGRYLARPAIAEYRVVSYDYHKVHYWYKDHRTGKRVDVVSPVMKFIYDLVQHIPPKHFRMVGRYGLYSRGKNKESQKVINLWRFMVHKQIEMTFPAEERKKKSYRQRMLESYGRDPMRCPCCKHRMLLVVIWHAEYGRIYYYDEEREYANQKKWGMRKGGKSTRTKERTG
>NZ_LN831776.1|WP_020426165.1|145075_146170_+|helix-turn-helix-domain-containing-protein
MDSEVLRQKLEQLTGKRTGIKQLGRQHSASLFGMGAEDQDQPVVHEGRLWVPLYENDGRVTAIWLELDGLTPMEVQLVNYAARNFAIALKATGLKEEGEIEARQLSGWLNAQLEQEKNEAEIPDEMTLKGRLVGEMIPFLLVSENVHNPQVTYRSLMKLLRSYFENEILLIPLQEKEWLILARKELLTGGDDKEDEEESADDLLAQTCMGLHELIASEWVGVFHLAVAPAIIPVKGLTGAVALLRETIILGRIFQVGDYIHLPWELHMERLVNSIPDERRRQLLGQIGDYSPVLADKEMLLTLETFFEMDCNVSETAKKLYIHRNTLLYRLDKIKQETGADVRSFGDAAIVKLAMLLYKVTKRK
>NZ_LN831776.1|WP_025709140.1|146279_147401_+|sn-glycerol-3-phosphate-ABC-transporter-ATP-binding-protein-UgpC
MAGVRLEHIFKKYPGSDKATVIDINLDIKDKEFLVLVGPSGCGKSTTLRMIAGLEEISEGKMYIGDRVVNDVAPKDRDIAMVFQSYALYPHMSVYQNMAFGLKLRKVKKEEIDKKVREAAKILDIEHLLDRKPKALSGGQRQRVALGRAIVRDPQVFLMDEPLSNLDAKLRGQMRAEITKLVKRLETTCIYVTHDQTEAMTMGDRIVVMYDGIIQQAASPEELYNEPTNLFVAGFIGSPTMNFINGTLSDVGGAVRFRAENLDVEVPGGKATLLRNKGYIGKEVIMGVRPEDIHEEPVFLEASPNTIFTSLVDVTENLGHEMLLYLSGLGAGTVIARVDGRSTTREGSKPKLAIDMNKIHIFDKESELNVLLG
>NZ_LN831776.1|WP_020425530.1|147733_148672_+|HPr-kinase/phosphorylase
MAKKVKVSELVQNFQLEVVSGHEGLKRPITVDDLNRPGLEMAGYFEYYPEERVQLLGKTELAFFSMLPDEERKSRIRGICNDNTPCIVITRALDVPQELIDISNEKGLPVLRSSMATTIFSSRLTSFLEGRLAPTATIHGVLCDVYGVGMLITGSSGIGKSETALELVKRGHRLIADDAVEIRQTSDNQLHGTAPELIRHLLEIRGVGIINVMTLFGAGAIRNHKRITLVVRLEAWQQDKQYDRLGLDEETTRIIDTDVPLVTIPVRPGRNLAVIIEVAAMNYRLKQMGFNAALQFTNKLTATISEDMDDLD
>NZ_LN831776.1|WP_020425531.1|148684_149716_+|prolipoprotein-diacylglyceryl-transferase
MFFSLAIDPIVFSIGSLPVHWYGLILGVGALAGLFLAIQEGKRFNIPQEFFMDMLLLGVPSAIIGARIYFVAFKWEDYKDNLIDVFKIWNGGIAIYGALIGAIICGIIYFRYKGYAFWRIADICAPGLLAGQMIGRWGNFVNQEAYGGVVEESFLRDKLHLPDFIVNQMYIGDAFHHPTFLYESLWSLLGILLLMVLRRQKFVRAGEIFLSYFIWYSIGRFFIEALRTDSLAFKGNSGLASFLNGLWSPMKWLGFEQGYLDPAYGNIRSSQLLALLTILAAIILIIVRRVTGQPKDHYSDPIVSTKAAAADAVVPESAAHTPQSAPQVRQPEPEKTPDELPKE
>NZ_LN831776.1|WP_020425532.1|149723_150377_+|pyrophosphatase-PpaX
MIECILFDLDGTIVNTNELIINSFMHTLKENNLPPLTREQIIPYMGTTLHQQLSAFSGLEDTSALELSYRSYNYAHHDELIGSFPHVNEIMEELAGRGIKLGIVTTKIRPTTIKALEMFDLLKYMETIVTVNDVVQPKPHAEPVLKAVSNLGVDPRRTLMVGDSPVDIQSAKAAGVCVAAVAWSLKGEDVLRKYEPDYIIHDMKDIFGIVDQGTMEP
>NZ_LN831776.1|WP_020425533.1|150373_150898_+|acyltransferase
MRRVTRYPVEGHNSLWYIYRTVSPWKGVRNFIFIQIARYCPILPVKNWIYRNVLGMKVGKHTAFGLMAMVDVFFPEKITVGENSVIGYNTTILAHEYLIKEYRLGEVIIGENVLIGANTTILPGVIIGDGAVIAAGSVVHKDVAAGSFVGGNPLRELRPSARNDRDDSEDNDVM

Crispr_ID: NZ_LN831776_3

• CRISPR_ID: NZ_LN831776_3
• CRISPR_location: 194997-195072
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_3

Consensus_repeat	Method
AATTAGTGATCCTTTTTCCAACTT	CRISPRCasFinder

spacers of NZ_LN831776_3

>3.1|195021|28|NZ_LN831776|CRISPRCasFinder
AGGCTGCGGAGACCGGGGTGTTCAAGCC

CRISPR arrays and Neighbor proteins around NZ_LN831776_3

CRISPR arrays

The CRISPR arrays of NZ_LN831776_3

>merge|NZ_LN831776|3|194997-195072|CRISPRCasFinder
AATTAGTGATCCTTTTTCCAACTTAGGCTGCGGAGACCGGGGTGTTCAAGCCAATTAGTGATCCTTTTTCCACTTG

>NZ_LN831776|3|3|194997-195072|CRISPRCasFinder
AATTAGTGATCCTTTTTCCAACTT	AGGCTGCGGAGACCGGGGTGTTCAAGCC
AATTAGTGATCCTTTTTCCACTTG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020425588.1|183629_184682_+|central-glycolytic-genes-regulator	unknown	unknown	gnl|CDD|367868
NZ_LN831776.1|WP_020427772.1|196346_197891_-|recombinase-family-protein	unknown	unknown	gnl|CDD|214861
NZ_LN831776.1|WP_020425581.1|191291_191525_+|preprotein-translocase-subunit-SecG	unknown	unknown	gnl|CDD|235881
NZ_LN831776.1|WP_020426309.1|199106_199271_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425585.1|187135_187891_+|triose-phosphate-isomerase	unknown	unknown	gnl|CDD|234589
NZ_LN831776.1|WP_020425587.1|184798_185809_+|type-I-glyceraldehyde-3-phosphate-dehydrogenase	unknown	unknown	gnl|CDD|273675
NZ_LN831776.1|WP_020425589.1|182432_183029_-|ATP-dependent-Clp-endopeptidase-proteolytic-subunit-ClpP	unknown	unknown	gnl|CDD|178955
NZ_LN831776.1|WP_020425584.1|187893_189438_+|2,3-bisphosphoglycerate-independent-phosphoglycerate-mutase	unknown	unknown	gnl|CDD|235463
NZ_LN831776.1|WP_052741400.1|197914_198505_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|238045
NZ_LN831776.1|WP_020426304.1|201144_201507_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426311.1|198782_198986_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197775
NZ_LN831776.1|WP_020427771.1|195351_195831_+|SsrA-binding-protein-SmpB	unknown	unknown	gnl|CDD|376590
NZ_LN831776.1|WP_020425583.1|189485_190772_+|phosphopyruvate-hydratase	unknown	unknown	gnl|CDD|234617
NZ_LN831776.1|WP_020426306.1|200182_200881_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425586.1|185920_187102_+|phosphoglycerate-kinase	unknown	unknown	gnl|CDD|234613
NZ_LN831776.1|WP_046506247.1|191776_194626_+|ribonuclease-R	unknown	unknown	gnl|CDD|273947
NZ_LN831776.1|WP_081487068.1|190882_191149_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426307.1|199845_200118_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426305.1|200896_201148_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426308.1|199267_199819_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020425588.1|183629_184682_+|central-glycolytic-genes-regulator	gnl|CDD|367868	pfam04198, Sugar-bind, Putative sugar-binding domain. This probable domain is found in bacterial transcriptional regulators such as DeoR and SorC. These proteins have an amino-terminal helix-turn-helix pfam00325 that binds to DNA. This domain is probably the ligand regulator binding region. SorC is regulated by sorbose and other members of this family are likely to be regulated by other sugar substrates.	2.24691e-63
NZ_LN831776.1|WP_020427772.1|196346_197891_-|recombinase-family-protein	gnl|CDD|214861	smart00857, Resolvase, Resolvase, N terminal domain. The N-terminal domain of the resolvase family contains the active site and the dimer interface. The extended arm at the C-terminus of this domain connects to the C-terminal helix-turn-helix domain of resolvase.	6.35067e-36
NZ_LN831776.1|WP_020425581.1|191291_191525_+|preprotein-translocase-subunit-SecG	gnl|CDD|235881	PRK06870, secG, preprotein translocase subunit SecG; Reviewed.	9.65683e-11
NZ_LN831776.1|WP_020425585.1|187135_187891_+|triose-phosphate-isomerase	gnl|CDD|234589	PRK00042, tpiA, triosephosphate isomerase; Provisional.	5.3851e-146
NZ_LN831776.1|WP_020425587.1|184798_185809_+|type-I-glyceraldehyde-3-phosphate-dehydrogenase	gnl|CDD|273675	TIGR01534, Glyceraldehyde-3-phosphate_dehydrogenase, glyceraldehyde-3-phosphate dehydrogenase, type I. This model represents glyceraldehyde-3-phosphate dehydrogenase (GAPDH), the enzyme responsible for the interconversion of 1,3-diphosphoglycerate and glyceraldehyde-3-phosphate, a central step in glycolysis and gluconeogenesis. Forms exist which utilize NAD (EC 1.2.1.12), NADP (EC 1.2.1.13) or either (1.2.1.59). In some species, NAD- and NADP- utilizing forms exist, generally being responsible for reactions in the anabolic and catabolic directions respectively. Two Pfam models cover the two functional domains of this protein; pfam00044 represents the N-terminal NAD(P)-binding domain and pfam02800 represents the C-terminal catalytic domain. An additional form of gap gene is found in gamma proteobacteria and is responsible for the conversion of erythrose-4-phosphate (E4P) to 4-phospho-erythronate in the biosynthesis of pyridoxine. This pathway of pyridoxine biosynthesis appears to be limited, however, to a relatively small number of bacterial species although it is prevalent among the gamma-proteobacteria. This enzyme is described by TIGR001532. These sequences generally score between trusted and noise to this GAPDH model due to the close evolutionary relationship. There exists the possiblity that some forms of GAPDH may be bifunctional and act on E4P in species which make pyridoxine and via hydroxythreonine and lack a separate E4PDH enzyme (for instance, the GAPDH from Bacillus stearothermophilus has been shown to posess a limited E4PD activity as well as a robust GAPDH activity). There are a great number of sequences in the databases which score between trusted and noise to this model, nearly all of them due to fragmentary sequences. It seems that study of this gene has been carried out in many species utilizing PCR probes which exclude the extreme ends of the consenses used to define this model. The noise level is set relative not to E4PD, but the next closest outliers, the class II GAPDH's (found in archaea, TIGR01546) and aspartate semialdehyde dehydrogenase (ASADH, TIGR01296) both of which have highest-scoring hits around -225 to the prior model. [Energy metabolism, Glycolysis/gluconeogenesis].	0
NZ_LN831776.1|WP_020425589.1|182432_183029_-|ATP-dependent-Clp-endopeptidase-proteolytic-subunit-ClpP	gnl|CDD|178955	PRK00277, clpP, ATP-dependent Clp protease proteolytic subunit; Reviewed.	3.11476e-150
NZ_LN831776.1|WP_020425584.1|187893_189438_+|2,3-bisphosphoglycerate-independent-phosphoglycerate-mutase	gnl|CDD|235463	PRK05434, PRK05434, 2,3-bisphosphoglycerate-independent phosphoglycerate mutase.	0
NZ_LN831776.1|WP_052741400.1|197914_198505_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	5.23089e-08
NZ_LN831776.1|WP_020426311.1|198782_198986_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|197775	smart00530, HTH_XRE, Helix-turn-helix XRE-family like proteins.	2.23255e-05
NZ_LN831776.1|WP_020427771.1|195351_195831_+|SsrA-binding-protein-SmpB	gnl|CDD|376590	pfam01668, SmpB, SmpB protein.	1.62148e-86
NZ_LN831776.1|WP_020425583.1|189485_190772_+|phosphopyruvate-hydratase	gnl|CDD|234617	PRK00077, eno, enolase; Provisional.	0
NZ_LN831776.1|WP_020425586.1|185920_187102_+|phosphoglycerate-kinase	gnl|CDD|234613	PRK00073, pgk, phosphoglycerate kinase; Provisional.	0
NZ_LN831776.1|WP_046506247.1|191776_194626_+|ribonuclease-R	gnl|CDD|273947	TIGR02063, Ribonuclease_R, ribonuclease R. This family consists of an exoribonuclease, ribonuclease R, also called VacB. It is one of the eight exoribonucleases reported in E. coli and is broadly distributed throughout the bacteria. In E. coli, double mutants of this protein and polynucleotide phosphorylase are not viable. Scoring between trusted and noise cutoffs to the model are shorter, divergent forms from the Chlamydiae, and divergent forms from the Campylobacterales (including Helicobacter pylori) and Leptospira interrogans. [Transcription, Degradation of RNA].	0

Protein sequences

>NZ_LN831776.1|WP_046506247.1|191776_194626_+|ribonuclease-R
MITQEQLLDFMRETAYKPLTYDELVSHFALEDSESFKAFEELLLALEQDGRMILTRNARYGVPERMDLVRGRVQAHAKGFAFLIPDDRDHPDIYMNANDLKGAMNGDIVLVRITSRSPSGGRMEGEVVRIVKRGVLQTVGVFQSLENYGFVLPDDKRINRDIFIPKQSFKGAVDGEKVVVRIVNYPEGRAAAEGEIIEILGHKDDPGVDILSVIRKHQLPEAFPAEVMREAEQAPDSITEEEIIQQGRRDLRGLNIVTIDGADAKDLDDAVNVSRLENGHYKLGVHIADVGYYVREGSELDKEAFDRGCSVYLVDRVIPMLPHRLSNGICSLNPKVDRLTMSCEMEFDEHMKVVKHDVFTSVIRTKERMTYSDVRKIVEDEDPELLERYSPLIEDFRLMKELAMKLRGARMRRGAVDFDFEESKIIVDENGKAIDIVKRERSVAEQIIEEFMLAANETVAEHFHWLKVPFLYRIHEDPDPEKLQNFMAFAANFGYHVKGRGNSVHPRALQDLLEQIQGTKEQTVISTMMLRSMKQAKYDAESTGHFGLAAEFYSHFTSPIRRYPDLVIHRVMREVIENGGALTEKRHEYLASRMPEIAQQSSERERVAVEAERDTEQLKKAEFMQDKVGEEFDAMVSSVTSFGMFIELENTVEGLIRLSALSDDYYHFDEAHMALIGERTSKVFRIGDEVKIRVAKVNMDDHTIDFELVDMKPRAAGEHRSFGGRGGKGGRAGGGFAKPFGSKAGGKGRAGGKGKPGSAAGRGKAGGAAHAGKGKSGAAARAGEAPRAAEEASGGAPAGGRGKRGGGGPAEAARRAFAAVNRGEAGGAGTPRERDRSGGRGRGGEAGGSAGGRGISFGFGSGKGGYGAPAGEQISELRGVDASTRFRSREDLGSGAAANGGGGKSRRKKNKKGGVFISPSVTPGNVERSDKSGNPEGSGRRKKKKKTQE
>NZ_LN831776.1|WP_020425581.1|191291_191525_+|preprotein-translocase-subunit-SecG
MDIFLKVLLLIFSVGLIAVVLLQKGKSAGLSGAISGGAEHLFGKTKARGMELVLQRVTVGLAAGFFIMSILVAVLVD
>NZ_LN831776.1|WP_081487068.1|190882_191149_+|hypothetical-protein
MMNAIISGIGVGMLLVLISWLLSRRGGQMKGFIFYPGLVGLIGGAILLVCSFSVIGGWEGMGYAFFSVPVIVISMLLLLFLGSFRRQT
>NZ_LN831776.1|WP_020425583.1|189485_190772_+|phosphopyruvate-hydratase
MTIISDVYAREVLDSRGNPTVEVDVYLESGAKGRAIVPSGASTGAHEAVELRDEDKNRYLGKGVLKAVENVNEIIAPEVIGMDALDQLGIDKLMITLDGTHNKGKLGANAILAVSMAVARAAAAALDVPLYVYLGGFNAKQLPVPMMNIVNGGAHADNNVDVQEFMVLPVGAPSFKEALRTGAEIFHALKSVLKGKGLNTAVGDEGGFAPNFTSNEDALSSIMEAIEKAGYKPGVDVFLGMDVASTEFFKDGKYHLEGEGKSFTPAEFVDLLTSWADKYPIITIEDGCSEDDWEGWKLLTEKLGNRIQLVGDDLFVTNTERLNKGIEEGIGNSILIKVNQIGTLTETFDAIEMAKRAGYTAVISHRSGESEDSTIADIAVATNAGQIKTGAPSRTDRIAKYNQLLRIEDELGELAQYNGLKSFYNLKR
>NZ_LN831776.1|WP_020425584.1|187893_189438_+|2,3-bisphosphoglycerate-independent-phosphoglycerate-mutase
MSAPKPVALIIMDGFGLRNTTEGNAVAQANKPNYDRYLKQYPNTTLTACGEAVGLPEGQMGNSEVGHLNIGAGRIVYQDLTRIDKSIREGEFFENETLVAAVRSAKSTGKKLHLYALVSDGGVHSHINHLFAMLDLAKKEDMHDVYIHAFMDGRDVPPDSGQKFIKDLIAKIEEVGVGKIATVSGRYFAMDRDKRWERVEKAYRAMVYGEGPKYTDALQAITASYQNSVYDEFVEPSVIVDSEGKPTATVESGDSVVFLNFRPDRAIQLSQVFTNSDFRGFDRGPLFPQNLHFVCLTTFSETVQGYVAYSPKNLDNTLGEVLVQQNKKQLRIAETEKYPHVTFFFSGGRDEELPGETRILINSPKVATYDLKPEMSAYEVAAACVAEIEADRQDAIILNFANPDMVGHSGMLEPTIKAVEVTDECVGKVVDAVVAKGGVAIIIADHGNADMVFDEQGRPFTAHTTNPVPFIVTTENVVLRESGILADVAPTILDLMGLPQPAEMTGQSMIASRK
>NZ_LN831776.1|WP_020425585.1|187135_187891_+|triose-phosphate-isomerase
MSRTPIIAGNWKMFKTVSEAEGFFAEVKGRAEVEGVETVICAPFTNLPALVAAAKGTSIKIGAQNLHFEDNGAYTGEISGVMLKDLGVDYVIIGHSERRAYFGETDEIVNKKMHAAFRHGITPIVCVGEKLEEREADQTKAVCKVQTEGAFAGLSAEQAASVVIAYEPIWAIGTGKSSTSQDANEVIAYIRTLVKDLYDQATAEAVRIQYGGSVKPENVTEYMSQSDIDGALVGGASLQPASFVSLVEGAK
>NZ_LN831776.1|WP_020425586.1|185920_187102_+|phosphoglycerate-kinase
MNKKSVRDVEVKGKRVFVRVDFNVPVEDGKITDDTRIRETLPTIKYLIENGAKVILASHMGRPKGQFVDSMRLTVAAVRLSELLGKPVAKADEAIGEAVKAKIAELKDGDVLVLENVRFYPGEEKNDPELAKQFAELADLFVNDAFGAAHRAHASTEGIAHFLPAVSGLLMEKELNVLGKALSNPERPFTAIIGGSKVKDKIDVIDNLLTLADNVLIGGGLSYTFTKAQGYEIGNSLVDNDKIDAALGFIEKAKKLGKNFVLPVDVVVADKFGADANTKVVDVTDIPAGWEGLDIGPKTREIYADIIKNSKLVVWNGPMGVFEIDIFAEGTLAVAKACATTEGYTVIGGGDSAAAAEKFHLADQMDHISTGGGASLEFMEGKALPGVEALNDK
>NZ_LN831776.1|WP_020425587.1|184798_185809_+|type-I-glyceraldehyde-3-phosphate-dehydrogenase
MSVKVGINGFGRIGRLAFRRIQNVEGIEVVAINDLTDAKMLAHLLKYDTTQGKFQGEVEVHDGFFKVNGKEVKVLANRNPEELPWGDLGVDIVLECTGFFTTKEAAEKHLKGGAKKVVISAPATGDMKTVVYNVNHDVLDGTETVISGASCTTNCLAPMAKVLNDKFGIVEGLMTTIHAYTGDQNTLDAPHAKGDFRRARAAAENIVPNTTGAAKAIGLVIPALKGKLDGAAQRVPVATGSLTELVTVLEKNVTVEELNAAMKAASDPDTYGYTEDEIVSSDIKGMTFGSLFDATQTKVMTVGDKQLVKTVAWYDNEMSYTAQLVRTLEHFAKLAK
>NZ_LN831776.1|WP_020425588.1|183629_184682_+|central-glycolytic-genes-regulator
MRNLLEIQKQLLPDLMETLKRRYTILHQIMLSDIIGRRTLAASLDMTERVLRAETDLLKSQGLIEIESVGMRVSDAGRRLLDLLEPIAKSLFGLDDLEEKIRTTYGLNKVIVVPGDCETSPFTKRELGRAGAKALLGVLRSEDTVAVTGGSTLAEMADQLTLPIPLSYKNAWVVPARGGLGESMEIQANTIASTMAKRIGANYRLLHVPDLLSEDAYQSLALDFNIGEIVQIIRRSRIIVHGIGDAMEMTRRRKLDEATIAEIQEEGAVAESFGYYFNEEGQVVHTMLTMGLRLEDIIRTEVVIGIAGGKRKAKAIHAMLRFGQEDILVTDEAAAVEIGKEIDNQNHTVL
>NZ_LN831776.1|WP_020425589.1|182432_183029_-|ATP-dependent-Clp-endopeptidase-proteolytic-subunit-ClpP
MSYIPMVVEQSNRGERAYDIYSRLLKDRIIFLGTEVNDVVANSIIAQMLFLAAEDPDKDIHLYVNSPGGSITAGMAIFDTMQYIKPDVSTICVGMAASMGAFLLNAGAKGKRFALPNSEIMIHQPLGGAQGQATDIEIRARRILKLRDKLNHILAERTGQPLERIEKDTDRDYFMSAVDAAEYGIVDKVIEKTLPSGV
>NZ_LN831776.1|WP_020427771.1|195351_195831_+|SsrA-binding-protein-SmpB
MGKKADGKVLAQNKKASHDYFIEDTYEAGLVLTGTEIKSLRNGRANIGDAFATIRNGEIHVHNMHISPFEQGNRNNPSDPTRTRKLLMHKVQIHKLLGQSKQEGYSIVPLKIYVRNGYAKLLIGLGKGKKQYDKRDTAAKKDAQRDIQRALREKQKIAR
>NZ_LN831776.1|WP_020427772.1|196346_197891_-|recombinase-family-protein
MPSTNKLIRAVAYPRYSSDNQREESIVAQMRAIEAYCQQKGYVLVNAYPDEEKTATTDRRPNFQRMIEDSNKKLFDVVIVHKLDRFARNRYDSAHYKRVLKRNGVRVESVLEHLDNSPESVILESVLEGMAEYYSLNLSREVRKGLRENAEQGTHTGGRPPYGLKVNPVTRMLEIDEQTYKAVQIYFDGIEADLSNDQIAAILNEKGYRTLNDRSFTSSSFATWGHNRKYKGDYTYDVSAPKDEDGKRNTNNKKPQEEQVLHEGRIPAIISSEQWDRVYRKLQDRKRKPGRMKAKVNYLLTGKIYCGACGALYSGNSYTNKKSSEGTVLTYYKCQDKCGNTSVRKDDIEAMVIQRLIEVCFSGEGIQEIIDKVQELYQKEKQQSVNDIEPIKRELAELEGKLKNWIEALGAGIKTVIENIKQAEQRKEALEYELDRAEVMQRVAVLDDTQIRSIIEMKKNLLLSGNEDEKKQVLQEYVDRVVIQPSSDINRFEAEITYRVFTNGAEGSRTPVRR
>NZ_LN831776.1|WP_052741400.1|197914_198505_-|helix-turn-helix-transcriptional-regulator
MEIVDNIKNLCYKNGTTIPKLEKELGFGNGTIYNWIKSSPSLEKLQKVASYFKVTIDDLVGWGHIYDLGSYIEDEREAQNVSLEDLSTAIQISPESLSQIENNKIPLTSELLGNITRYLGMTVQEFLIKYEMYEGAITQYYKGDINAYLDYLKHEEETVQINKPNIDEEDWTDKELEELKRFKEFLRMKRDHNTEK
>NZ_LN831776.1|WP_020426311.1|198782_198986_+|helix-turn-helix-transcriptional-regulator
MTHYSEFGAEARKVMLQKKIKMKDVASELGVSVTYVSEIFKGTRPGERQKPLIAKMLGMESEVVHES
>NZ_LN831776.1|WP_020426309.1|199106_199271_+|hypothetical-protein
MTINQQAESADHVWRRLELRRRRWQLLNGRLIVDEPEAAVWWLDKEIAEMEAGQ
>NZ_LN831776.1|WP_020426308.1|199267_199819_+|hypothetical-protein
MKTLHFTYDPLRLVRIVLQRHVEETIQGRFYKAKQFACYEYLAKLSDEGLENLLQEYTKRHELEAITLADWRKDGKLIFDIIFEQPEYQQLEIDFKKRGYGITGLGVLDVESNTFYECGFAHHWQAIQNIIEKSYPRFHEPLQRMYFDETLTEHDGLTREELENFIMTNFELYGGTKPLQEYL
>NZ_LN831776.1|WP_020426307.1|199845_200118_+|hypothetical-protein
MNEPVTKPLGWGMVAVMIDNPVVGGKQLHLFEAESTMSGAYVPPKQIKIDEVEKLRDFLIEQMPPDDLVNLLSTLEKAIHEKDDPSAATV
>NZ_LN831776.1|WP_020426306.1|200182_200881_+|hypothetical-protein
MGCDIHLFVEKRINGVWQVERGVNEPEIEEVRGFIDKSKERGESSAYWERLLEELRQGTMDYIYDGRHYLLFEVLAGVRAAHDLKPVSNPKGLPEDISPEAGESAESWGGDGHSHSWLTAAELLAYNWDQTITREGWVGVEQFKKYLEDGEPSMWSGGVGGGGTKYISNKEMKEGIRDGFLFGDPRQYYTLIHWNKSLRDALGKWCSWSLPKLAELAGDDPESARIVFWFDN
>NZ_LN831776.1|WP_020426305.1|200896_201148_+|hypothetical-protein
MENQVKRKSIGEVLATIDPEKVNLQLVKPALMEVARSNTKRSGFLKIAVDDDVAVDCFQAMPDKIRFIISIDREDWNRAVVSE
>NZ_LN831776.1|WP_020426304.1|201144_201507_+|hypothetical-protein
MKAYDFQKAKLLIEQDREQIQEAALGMYEDWFWTAEEVFNDQEGFVRDLETVELIGGINESSWATPCLRITYRDGNESCIGCFKDDGSPSERGFVMPLGVLSGPAQDRMPPLTSKEGRHD

Crispr_ID: NZ_LN831776_4

• CRISPR_ID: NZ_LN831776_4
• CRISPR_location: 399007-399081
• CRISPR_type: Unclear
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: Cas14u_CAS-V

Consensus repeat of NZ_LN831776_4

Consensus_repeat	Method
AATTAGTGTCCATTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_4

>4.1|399030|29|NZ_LN831776|CRISPRCasFinder
CATCTGCTCGAGGATAGGGTACTCCGGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_4

CRISPR arrays

The CRISPR arrays of NZ_LN831776_4

>merge|NZ_LN831776|4|399007-399081|CRISPRCasFinder
AATTAGTGTCCATTTTTCCACTTCATCTGCTCGAGGATAGGGTACTCCGGCAAATTAGTGTCCCTTTTTCCACTT

>NZ_LN831776|4|4|399007-399081|CRISPRCasFinder
AATTAGTGTCCATTTTTCCACTT	CATCTGCTCGAGGATAGGGTACTCCGGCA
AATTAGTGTCCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020427985.1|404025_405297_-|GTPase-HflX	unknown	unknown	gnl|CDD|274455
NZ_LN831776.1|WP_020427988.1|399342_401070_+|hypothetical-protein	unknown	unknown	gnl|CDD|366376
NZ_LN831776.1|WP_046500972.1|405366_405597_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_039790964.1|411576_413892_+|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_020427212.1|391990_392884_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_081487100.1|385971_387447_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270451
NZ_LN831776.1|WP_144412147.1|388371_390591_+|collagen-like-protein	unknown	unknown	gnl|CDD|236140
NZ_LN831776.1|WP_020427987.1|401059_402124_+|hypothetical-protein	unknown	unknown	gnl|CDD|226678
NZ_LN831776.1|WP_020426497.1|380769_382389_-|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_020426495.1|384434_385391_-|IS200/IS605-family-element-transposase-accessory-protein-TnpB	Cas14u_CAS-V	-	gnl|CDD|223747
NZ_LN831776.1|WP_046500978.1|409748_411395_-|hypothetical-protein	unknown	unknown	gnl|CDD|227059
NZ_LN831776.1|WP_020427213.1|392940_394482_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|378792
NZ_LN831776.1|WP_020426496.1|382363_384217_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_020427984.1|405900_406695_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426494.1|385396_385795_-|IS200/IS605-family-transposase	unknown	unknown	gnl|CDD|376616
NZ_LN831776.1|WP_046500975.1|406722_409752_-|DEAD/DEAH-box-helicase	unknown	unknown	gnl|CDD|223627
NZ_LN831776.1|WP_085981682.1|414084_415080_+|tripartite-tricarboxylate-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270234
NZ_LN831776.1|WP_020427211.1|390805_391792_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_LN831776.1|WP_046500969.1|394650_398169_+|hypothetical-protein	unknown	unknown	gnl|CDD|271147
NZ_LN831776.1|WP_020427986.1|402169_403888_+|hypothetical-protein	unknown	unknown	unknown

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831776.1|WP_020426495.1|384434_385391_-|IS200/IS605-family-element-transposase-accessory-protein-TnpB	Cas14u_CAS-V	-	2.3e-43	143.7	6.4

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020427985.1|404025_405297_-|GTPase-HflX	gnl|CDD|274455	TIGR03156, GTP_HflX, GTP-binding protein HflX. This protein family is one of a number of homologous small, well-conserved GTP-binding proteins with pleiotropic effects. Bacterial members are designated HflX, following the naming convention in Escherichia coli where HflX is encoded immediately downstream of the RNA chaperone Hfq, and immediately upstream of HflKC, a membrane-associated protease pair with an important housekeeping function. Over large numbers of other bacterial genomes, the pairing with hfq is more significant than with hflK and hlfC. The gene from Homo sapiens in this family has been named PGPL (pseudoautosomal GTP-binding protein-like). [Unknown function, General].	1.35204e-169
NZ_LN831776.1|WP_020427988.1|399342_401070_+|hypothetical-protein	gnl|CDD|366376	pfam00933, Glyco_hydro_3, Glycosyl hydrolase family 3 N terminal domain.	1.18537e-58
NZ_LN831776.1|WP_020427212.1|391990_392884_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	7.20054e-61
NZ_LN831776.1|WP_081487100.1|385971_387447_+|extracellular-solute-binding-protein	gnl|CDD|270451	cd14748, PBP2_UgpB, The periplasmic-binding component of ABC transport system specific for sn-glycerol-3-phosphate; possesses type 2 periplasmic binding fold. This group includes the periplasmic component of an ABC transport system specific for sn-glycerol-3-phosphate (G3P) and closely related proteins from archaea and bacteria. Under phophate starvation conditions, Escherichia coli can utilize G3P as phosphate source when exclusively imported by an ATP-binding cassette (ABC) transporter composed of the periplasmic binding protein, UgpB, the transmembrane subunits, UgpA and UgpE, and a homodimer of the nucleotide binding subunit, UgpC. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	8.28033e-44
NZ_LN831776.1|WP_144412147.1|388371_390591_+|collagen-like-protein	gnl|CDD|236140	PRK08026, PRK08026, FliC/FljB family flagellin.	8.17346e-06
NZ_LN831776.1|WP_020427987.1|401059_402124_+|hypothetical-protein	gnl|CDD|226678	COG4225, COG4225, Predicted unsaturated glucuronyl hydrolase involved in regulation of bacterial surface properties, and related proteins [General function prediction only].	9.74818e-68
NZ_LN831776.1|WP_020426497.1|380769_382389_-|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.20885e-46
NZ_LN831776.1|WP_020426495.1|384434_385391_-|IS200/IS605-family-element-transposase-accessory-protein-TnpB	gnl|CDD|223747	COG0675, COG0675, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	1.06499e-26
NZ_LN831776.1|WP_046500978.1|409748_411395_-|hypothetical-protein	gnl|CDD|227059	COG4715, COG4715, Uncharacterized conserved protein [Function unknown].	1.83315e-05
NZ_LN831776.1|WP_020427213.1|392940_394482_+|ABC-transporter-substrate-binding-protein	gnl|CDD|378792	pfam12010, DUF3502, Domain of unknown function (DUF3502). This presumed domain is functionally uncharacterized. This domain is found in bacteria. This domain is about 140 amino acids in length. This domain is found associated with pfam01547.	9.70836e-47
NZ_LN831776.1|WP_020426496.1|382363_384217_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	1.39799e-59
NZ_LN831776.1|WP_039790964.1|411576_413892_+|AraC-family-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	7.9581e-25
NZ_LN831776.1|WP_020426494.1|385396_385795_-|IS200/IS605-family-transposase	gnl|CDD|376616	pfam01797, Y1_Tnp, Transposase IS200 like. Transposases are needed for efficient transposition of the insertion sequence or transposon DNA. This family includes transposases for IS200 from E. coli.	6.68313e-48
NZ_LN831776.1|WP_046500975.1|406722_409752_-|DEAD/DEAH-box-helicase	gnl|CDD|223627	COG0553, HepA, Superfamily II DNA/RNA helicases, SNF2 family [Transcription / DNA replication, recombination, and repair].	6.23623e-116
NZ_LN831776.1|WP_085981682.1|414084_415080_+|tripartite-tricarboxylate-transporter-substrate-binding-protein	gnl|CDD|270234	cd07012, PBP2_Bug_TTT, Bug (Bordetella uptake gene) protein family of periplasmic solute-binding receptors; contains the type 2 periplasmic binding fold. The Bug (Bordetella uptake gene) protein family is a large family of periplasmic solute-binding (PBP) proteins present in a number of bacterial species, but mainly in proteobacteria. In eubacteria, at least three families of periplasmic binding-protein dependent transporters are known: the ATP-binding cassette (ABC) transporters, the tripartite ATP-independent periplasmic transporters, and the tripartite tricarboxylate transporters (TTT). Bug proteins are the PBP components of the TTT. Their expansive expansion in proteobacteria indicates a large functional diversity. The best studied examples are Bordetella pertussis BugD, which is an aspartic acid transporter, and BugE, which is glutamate transporter.	1.97795e-102
NZ_LN831776.1|WP_020427211.1|390805_391792_+|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	1.20008e-121
NZ_LN831776.1|WP_046500969.1|394650_398169_+|hypothetical-protein	gnl|CDD|271147	cd04081, CBM35_galactosidase-like, Carbohydrate Binding Module family 35 (CBM35); appended mainly to enzymes that bind alpha-D-galactose (CBM35-Gal), including glycoside hydrolase (GH) families GH27 and GH43. This family includes carbohydrate binding module family 35 (CBM35); these are non-catalytic carbohydrate binding domains that are appended mainly to enzymes that bind alpha-D-galactose (CBM35-Gal), including glycoside hydrolase (GH) families GH27 and GH43. Examples of proteins which contain CBM35s belonging to this family includes the CBM35 of an exo-beta-1,3-galactanase from Phanerochaete chrysosporium 9 (Pc1,3Gal43A) which is appended to a GH43 domain, and the CBM35 domain of two bifunctional proteins with beta-L-arabinopyranosidase/alpha-D-galactopyranosidase activities from Fusarium oxysporum 12S, Foap1 and Foap2 (Fo/AP1 and Fo/AP2), that are appended to GH27 domains. CBM35s are unique in that they display conserved specificity through extensive sequence similarity but divergent function through their appended catalytic modules. They are known to bind alpha-D-galactose (Gal), mannan (Man), xylan, glucuronic acid (GlcA), a beta-polymer of mannose, and possibly glucans, forming four subfamilies based on general ligand specificities (galacto, urono, manno, and gluco configurations). Some CBM35s bind their ligands in a calcium-dependent manner. In contrast to most CBMs that are generally rigid proteins, CBM35 undergoes significant conformational change upon ligand binding. GH43 includes beta-xylosidases and beta-xylanases, using aryl-glycosides as substrates, while family GH27 includes alpha-galactosidases, alpha-N-acetylgalactosaminidases, and isomaltodextranases.	9.06136e-11

Protein sequences

>NZ_LN831776.1|WP_046500969.1|394650_398169_+|hypothetical-protein
MIKKTAVLLTLLCVLMTVLMPGGRIVSADPPGTAAGKQETSMTSKHAKSEGPVTRPVSAALLPGTVATATYDPPGLLWQVGTADNSSAEFTVYNNVYSNLTLPLPAGSWNTVSKGMKADVNGTVNLTFDLTAVPEHGMEFSFKVIDASTAIPQLAVFTNGLMSGLIQITGLNNGEAALENTWKQTYRLYIPKEQLHTGQNELKLMVDRGLYADPQAPGYDGDQYLWFEWDYFKLKSLEEQAEEPIHGRYVHLGTTLAAATFRYDENAIRHLAPMTKWMGIAYSGNWMRASFWSDTSAGWDPQGRNYLETLRDLNLEPMVNIIGGNWKNNADLVGGTISTALRNYYSAFVSKFGDLYQYAESGNEPGLFRWSQQSVLAIHELMDQERQTNNQPYLKIVAPGWAYWPYNGIPDGWERDAAQRKEIEALSDVTNGHSYGGTGVQPLPGGSLYENLQVYGEADEGFGKEMAMSETGSNDNHSDNTKYGTYAHRFASAFDRELRGDIGYVDHIMQHAAFFNDGTEFGLFNSGINWNTHRFEDTAAVAANTNEPGETRLKTFRRLAAAYATHGRPLSYEILNPLDLNGKKAYFRAVDTSALGTSVIGASADKILLNFVNFETGPVTMQVRVKMPECGEYTGERFGPGDTYAAAHSKVQLTATPDLTLTVTLGAGETVQYILDELETEAPSAPTSPAAVAVSHEQVKVTWNAATDNDSVVTYNVYRDGGTEPVMTIPGRITFYNDYTVTPETVYSYRIQAVDDSGNVSPLSTAVSATTLPMPITPHVPGDPTKFEAEAAAFAAPLKIGHYSIASGGRVVEQTHAGGLTVQGFYSENGGSYTLTIAYASNQESKKNILINGVKQTTVTLPSTGSWNSNFTARQYGITLQPGYNMISFTSAGNGANLDYFKLEEGAYVPVSAWYTVEHDHPYIDYTGFTTASNGVSHVTYAPDATAVFNFKGIGVRWRSDIKSDMGSADVYVDGQYRETIVIPQAGLEGDNKIVYELTGLEYGLHRIEIRGTDGLVMVHGFEFESYEPILPAPLPDLTVTDIGWNIVNSDGTPSSHTIPQLGDSLIFWAKVKNIGVRPTPLNTSTGLGQITGGAFSVNGGVVSWTDTNNTVIQPGEEITLTANSSAQGTPRWAVPTIGDFTIGFFVNDIWRYEEMNKENNKLSETLSINLN
>NZ_LN831776.1|WP_020427213.1|392940_394482_+|ABC-transporter-substrate-binding-protein
MAGKKGTGLLLSFVLLIGLSLSGCGGSNSNNEVAPTGTQADSTAAPAASDKAVATEKTNELEQVELSLYLPGGPDKDVASVEQAINEYLKDKINATIKINQLSWDKPADKVNLMIQSGEVFDMVYTWNFMTNAAKGAYLPLEELLDTYAKETKAQINPAYLQAATVNGHLYAVPTEKELGQSVGFAFDKAIVDKYGFDVNSIKKLEDIEPMLKTIKEKEPAITPLFMNHTDSLNWFTVYPDSEDLDGSNEIPTLLDYKTMKVFNEYDTPEILARLKLIREWYKAGYINKNGATDKTELKDAVKSGKAWFTYGNMNPTSTNDWTRLAEKPMVIKTLLPVQVSTKSLQGSMLAISRTSKNPERAMMFINLIHTDPVLYNLLTFGIEGKHYKKVGDNTVEFIPDSGYNSVSSWMIGNVLLNYLNKDEDPKRVQLYTDWNKNSKVSPVIGFVFDSTKVQSQIGALINITKQYKNTLYSGEKDPEPILKEMNSKLKAAGLDAVISEIQSQMDAFLAAK
>NZ_LN831776.1|WP_020427212.1|391990_392884_+|carbohydrate-ABC-transporter-permease
MTNNEISRPTNIILHIIFIILSITCLLPIVLVFMISITDYDSIVLNGYQFIPEKLSLEAYAYIFKDYAVIVKAYGVSIFVTVAGTLLSVFISSLYAYPISRADFKYKGFFAFLIFFTMLFGGGLVPWYMVYTQVLDLKNSIWALIVPMLLSPFNVLIMKTYFQMSVPPALIEASKIDGAGELRTFFRIVFPLSLPVFATIGLFNTLHYWNDWFNSMIFITDTDLYSLQYLMYKMISQADYLSRNGALIQGSATELAKLPGETIRMAMALIGIGPIVLAYPFFQRYFIKGLTLGSIKG
>NZ_LN831776.1|WP_020427211.1|390805_391792_+|sugar-ABC-transporter-permease
MITHEKRNALDTRLHLPVRLHPKRSSMLRHLLKHKVLLLMLLPGVVFLLINNYLPMFGIIIAFKNINYVDGILGSPWVGLDNFKFLFATSDAWIITRNTVLYNFVFIILNLVIAVSIAIALNELKNKLAAKFYQSVMFFPYFLSMVVVSYLVFAFLNVEYGFINKGILAMFGLNELNWYSEPKYWPFILPLINLWKGVGYGCVIYLAAIIGIDSEYYEAALIDGASKWKQILHITIPLIRPVIIITTILAIGGIFRSDFGLFYQTTLNSGALYPTTLVIDTYVYNALINMGNLGMSAAAGLYQSIVGFFLVLGSNWIVRKVDKDQAVF
>NZ_LN831776.1|WP_144412147.1|388371_390591_+|collagen-like-protein
MDAFEFIITTASPSPADDPVQVSLWGKSSTGQLVTAHRLVSAELLGETPGATGATGATGATGATGETGATGVGVTGATGETGATGVTGATGATGETGATGVTGATGATGETGATGATGVTGATGETGATGVTGVTGATGETGATGVTGATGATGETGATGATGATGATGETGATGVTGVTGVTGVTGATGETGATGATGATGATGETGATGVTGATGATGETGATGATGATGATGETGATGATGATGATGETGATGATGVTGATGETGATGATGATGATGETGATGATGVTGATGETGATGVTGVTGATGETGATGVTGATGATGETGATGATGATGATGETGATGVTGVTGVTGATGETGATGVTGATGATGETGATGVTGATGATGETGATGATGATGATGETGATGVTGVTGATGETGATGVTGVTGATGETGATGVTGVTGATGETGATGVTGATGETGATGATGATGATGETGATGVTGATGATGETGATGVTGTTGATGETGATGVTGATGATGETGATGVTGVTGATGETGATGATGVTGATGETGATGVTGATGATGETGATGATGATGPNVAAEGFSAFLPTLSASASTQLAGWTVTSPYYDSTSFDETTGNYTVPVTGRYSFEATINYSTTAAISVALGAGVNPAFVIRRTSPTTLDLVNGLFPLLNVNIALVLTLRTILGNGTVTLTGEFDLTAGDVIGLFYEADGLTVPLDLGGTSSGVVWSVHRFI
>NZ_LN831776.1|WP_081487100.1|385971_387447_+|extracellular-solute-binding-protein
MMKRLLFYIIGLSLCGLIVYALAYDRPLLVEFSPEPVPKAVPKIQVRIALNDWTENLEVKNAIRQFNESNPDHIEIVMVNLSADTYNDMLNMLMTSGQGPDVFSVDNGWLATYVNKGYLTNLNAYLGPADLNRFPEWARDYAHSSLFKGGVYFMPSSIETVRLIYNKQLFRSAGLDPEQPPVTFAEVKQAAARISRAGVGVNKYGFALAAGDSQDSLQTGLEMSNTYSGVYLYNYRTGRYNLSVYAPWLQLLLDMKAESSLYPGETLLKRDSALRQFADGNIGMMYATSKDYVKLQEYMPKDDWGVALPPVTSSASRGSGALMVIPHSPLAVNSSAPDQEAAVKVWKFLQSEAFLNILFQQALALPVVDGITDLPGQVPGLGHFKEFYPTAEESIYPLPPQIMDQYDPNTVSVEPRDSGDRPRMQLYLQILSGGVSAGEGLRAESDRLNQMLDIAATGYSFKHEEYIYPDFNPRAPLKAESLESRLNSGQE
>NZ_LN831776.1|WP_020426494.1|385396_385795_-|IS200/IS605-family-transposase
MGQEYRRTTTTVSLINYHFIFCPRYRRKVLSGQVEVRFKELVQELCTQNDWHIAVIEVMPDHVHLFLNVLPTDSPADIMGKLKGATSRDLRQEFIHLNHLPSLWTRSYFVSTAGNVSSETIKRYVEEQKTRG
>NZ_LN831776.1|WP_020426495.1|384434_385391_-|IS200/IS605-family-element-transposase-accessory-protein-TnpB
MSQTLTIKIKLLPTREQASMVKNQAIKDAKSVFKKAKKSKFTIVPVLKKPVCIWNNQNYSFDFTHISMPLMMNGKVAKTPIRALLIDKDNRNLGLLKHKSGTLRITQKSEKWIAQISVTVPTSEKTGTKIMGVDLGLKVPAVAVTDDDQTCFFGNERQNKYIRRKFQSKRKKLGQRKKLNAIVKLDDKEQRYMKDQDHKISRAIVQFAVEHQISVIRLEQLANIRQTARTSRKNEKSIHMWSFYRLSQFIEYKAKLAGVKVEYVNPAHTSRTCPKCSEKNKAQDRKYICSCGFETHRDRVGAMNIRYAPVIDGNSQSA
>NZ_LN831776.1|WP_020426496.1|382363_384217_-|sensor-histidine-kinase
MKKLFDTLSKTLFLYNFSIRSRLILYFLFLVLLPTTIISVTVYNKSADIITRNVHTSIENNLNLVQDNLAQRFAAADNAMISLYLNTEFADLISSNRPTDSTGIINELAALNKILETFSGSGTAGGSFVPMLYMLNRPEYTQYNFSRRVFNIDLISLKPWYLGIPARSDFTVVGLSSLDSRFTLKFAKRLFGIRHAQLPYVGLLTIDIPVTEFDNLLDHYKPTAGSRIYIADQTGTIAISPDAALLGQNISTQDYYSQMKTAEGGGTLHSFRQVIQGGNMLVSYIKIPETGWTILSFSPVKELNGELASFQRVMYIAISICMLISLMMALLLSENISAPIRKFIQSMSHAESGNFNIIIRYRRKDEFSYLFNRYNKLLQQIKALIDKLYVTELRKKEAELKTLQAQINPHFLYNTLDSINWIAINHDIPEISNMVTSLSDFFRYSLSKGRNIIPLRDELRQVDSYLQIQQFRFQDKLEYELEETDPKVLEECLVVKLSLQPLVENAIIHGIQKRRGKGKIRIRVVRSQDILCVSVFDDGVGADPERLNQLLTDKQPGNESYGIRNVHTRIQQFFGEAYGIRYYANDEEQRGLLAVVRFPVVTTWNEVMEDADDDRGR
>NZ_LN831776.1|WP_020426497.1|380769_382389_-|response-regulator
MLTMIVADDEPFIRRSLIQVFNWQEEFGIEIIGEASDGQEAYELCMELQPDILFTDIMMPMLGGLEVAEKLKAGQCRTRIIIISGAQDFSYAQSALKVNAEGYILKPVKLPELREVFQEVVSRLRGEKDQQMNVEQLRRQVQTHMPLIREKFLQNWAAGLYRDEGELWEKIGYFQLPFRPGDVLTAGVLQLDDYQSAVDKFSEDDKQLLYFSIQNIISECLEHPPGGVSFAASENEFMIIFGPDEGASPGEGAIAGFCEKIIGSIHKYLRLDASIGVGRACTRVSELEDSYKDALAALVHTFYTGSRSILHIRDIQPGTETLQSAFFYKFHARLMNELKAGHTEQVMELLEKLFDRLTAPKLQIDYVQSICAEMIFTSARALYELDEDIERVLQDRLTIMDTLYRHKNLSGLKAYVLSLFYDLSAYMAGKNSSRNSKTINRIRAIVQEGYAQELSIARIAEEVFLTPNYISLIFKKETGETLTDYITRIRIDKAKELLSTTDLKVMEISGLVGYENPHYFSTVFKKSVGVHPLKYRSGK
>NZ_LN831776.1|WP_020427988.1|399342_401070_+|hypothetical-protein
MHRPLTREEQDWVERTLTSMSLREKIGQTMQDHAGRLPFKGNDEEALAAYLKTYPVGSFFIGGEVIQKAAGKAEEYRDWAEQLQRISKYPLLFSGDLEFGAGSAVKSLTAFPPLLGLAAADDEALAYEYGKFTALEGRAAGFTWALAPGTDLLLNWMNPVITTRCLGDDARRAARLAGAVMRGMQDHGLAACAKHFPGDGVDYRDQHIVTTINGLSEEEWFAAYGQVSQHMIDQGVLSYMTGHIALPWLEGGTQEEKPVPATVSERITTGLLRERMGFAGVVLSDALDMGGFLAWGSYEKRMVDCFNSGTDVLLWPGVEYFGVMEQAVSEGTVLMERLDASVRRVLELKALLGVHRVDQKGRDPQAVPLLNDRLPPKLDLEARQLSRTIAERCITLVRNRGGILPLDPQTTRRVLVVLLNKVTEGRKYERMNVFVELLRARGLQVDILDEFEPLGTLRKWELSGIRWDAAFAPYFLPLHGMMNTARPVGEAAKAIWAMQHAETIRPIGISFATPYLLQDMPFLDALINAYSLHEETVELTVKALFGEVPFQGQSPVKADPLDGSPDLKGVHHHEH
>NZ_LN831776.1|WP_020427987.1|401059_402124_+|hypothetical-protein
MNTERKLAETLDLLFRYMILEEHKGHWGMDIDHWDWVPGVGVISLMEYATASGRGEVLDYLLQWVNRNKRKAEGAKVINALAPFALFPELYRQTGDPWFLQKAMSTADWMLNAAPVTREGALEHTVTENVDFPEQVWADTVYMAVLFLARLGGLTGEPRLADAAVQQTLLHLQLLQDPESGLLYHGWNSRAGNHMSAVHWARANAWITLAVPQIVAELREAVAIPEELYSRYRLLAAGLLSCQAGNGLWHTVLNRPDFVQETSGSAGIACGFIKGVEQGLLESSYLDGARQTVQGILPLIAENGEVQGVSGGTPVMPSADAYNTIEIYPTLYGQGLVLQLFTQAPDLLSGTRSA
>NZ_LN831776.1|WP_020427986.1|402169_403888_+|hypothetical-protein
MKKTAEQLNKHEAIDHQRMLIRKMQSLGSRYNPELRMLQSPFSSPGYHTTLRGVEFIHSTRDSLSYALGLLDTELAEHEPRAFGIIAQVVSLQDTDRSRDTFGIWPWFYEEPLAQMAPPDWNWADFCGSRLIQALKRHGNRFPEALRKAVADSVSYACEAIIKRNVGPDYTNIAILGAFVTRIAGEQLERGDFADYGLKRLQKLYDYTMKRGAFQEYNSPVYTYIAILELSKLHSETMDDQVRGLTRELIDLTWRSVAGYYHPATGQWSGPHSRSYETLLNNQSKAFLQVATRGTVMFFGWEELPYEEEWYKSGFECPAACLEAFSVPRTQEIRQLYEGDETDGTGKWAVTYMTPRVSIGSFTNSDLWNQRRPLLVYADNNGLPVYMQLRCLHDGYDFCSARFKSKQEQGQVLFGIDFITDGGDTHPNLDLTGGAIEAGDLRLRLEIGGQLKGVAAKSTAEGASIRVGEAHCVLTTWFAAFTGHSGAGRDWTWEVHETGDRILVELILYSGPRKRIDLHALQQAAMVFSLDMEKPPGSSGPQIEVAEGKLRVSASGEEAEAFSLRLRPGQAE
>NZ_LN831776.1|WP_020427985.1|404025_405297_-|GTPase-HflX
METVHQKAVIVGVQLQNDKDFAYSMEELRNLAAACELEVVGELSQKSSRINPAHYIGTGKIGELEALLEALEAPIVIFNDELSPSQIRNLESALDRQVIDRTVLILNIFAERAKTKEAQLQVEVAQLQYMLPRLAGMRESLGRQGGGAGLKNRGAGETKLELDRRRIEERITALQLELQTQVARRQVQRKQRRKNEVPVVCLVGYTNTGKSSLMNTIMETYHPGSQKGVLAKDMLFATLETSVRSIELPDRKTFLLTDTVGFVSQLPHHLVKAFRSTLEEVTEADLLIHVADISDPQVGQHIAVTEETLKALGADGIPAIKAYNKADLTELPYPVVKENTVTLSAKQKSGIAELIDLVRQHVFNDYIRCEILVPFDRGSVVSYFNDHADVQEVSYEEQGTRLKLECRAADYERFKSDFVVISQ
>NZ_LN831776.1|WP_046500972.1|405366_405597_-|hypothetical-protein
MNQTSGGQIVTPASPLGILAAPSGNHNEPPRRQVQQLAVLPGRRIFLHTFIVAMEMPKKGLGECRFLRWPYSVVLY
>NZ_LN831776.1|WP_020427984.1|405900_406695_+|hypothetical-protein
MPYLTTNTLTSRPTRGLGTISQVIIKTVNNGSSKAVVYITGLNNDVTPETLFAQELFEVNYREVVTRIYNITQTYFQFNAVYSQEQTQIQIFLVDSAGVLSQVALEQLEVSRITSEFRENIAVTASDFALISFRRNTAVVIPEAVAAEIKPDSLEILASTPIRYKIVGGGTVNGTFVNFPTPTTAISATETALQVNYTCTAVTGGRVITQGIGSGIAGAYQNVAANLTSQQLLYNLTDEIITLVVSSLAGSDNLAAVFRMSEEW
>NZ_LN831776.1|WP_046500975.1|406722_409752_-|DEAD/DEAH-box-helicase
MSMHTRTITVQLALSQYGDALIYGINERDDYVSGLLLKQQLFAWHEESFYGTELTTQNADGVELVILPAEQVIPFFADLKVLQHIGWSWEGNAALVTALAPVLAALLDEKQYVPSFSAFREGQLRWDWDGQALAGAVRGSRTAAEALRGLQERSTLAEGLQAAFSAAVFQRYYSTEAEAGDLRSEFPLLFSRSGLAAAGMDADSWLMSIGWKADSAPFRPALQLLEPDGDSSWRLQLLLQDKRDESALVPLRLSDDGEPHGRWPAPWAEHVRERAAGWLSRLRDSLPGGHIGRGRDVLGESLSDEVAWRFLTVDSRRLLEAGWQVLLPAWWEAASRKKPRLRAKISAGEGSRGGRSLFGLDALVDFDWRISIGDADLSEAEFAELVARGERLVKFRGQWIPLDPALLAQIQRAMAGMDKSQGLSFQDVLQLHLLGSSEDEAAEAAAEQAEEDAARFRLEVELNAHLVKLIGQLGQRDRWPQPAVPAGLHAELRSYQQEGFAWLAFLRRFGLGAVLADDMGLGKTVQLIAYLLHLKELEEAAEADPAAGRVRQTDPPGWPSLIICPTSVLGNWQKELQRFAPSLKVMLHYGSKRLDAGYFYGVASQADVVLTSYATAALDQELLKQFTWAAVCLDEAQNIKNAGTKQSSAVRSFPALHRIALTGTPIENRLSELWSIYDFITPGYLGSAKSFQDRFANAIEKERDAKRTADLQKMVKPFMLRRKKKDPAIQLDLPDKNEMKTYVHLTAEQAALYDQNVNGLLERMQKLEGIERKGAILAALTSLKQLCDHPLLLSKDALPEAESEGRVDTAALIERSAKLERLLAMVRELREENERCLIFTQYVGMGRMLQAVLSQELQEPVLYLNGSTPKSARDRMIEQFQTPAPPPGEVPPAGGRTQSDQPNVFILSLKAGGVGLNLTAANHVFHFDRWWNPAVENQATDRAYRMGQTKDVQVHKFISLGTLEEKIDEMLESKQQLSDDVISSSESWITELSTDALKDLFTLRREWVG
>NZ_LN831776.1|WP_046500978.1|409748_411395_-|hypothetical-protein
MQPKTMINDAEWDKLISDVAYYFDDLTLKRGFQYYKQNRVRSFRMISSRRVMAVVEGREDYAVSMELDSLTDSHCDCPVQGPCKHMAAVLMSVAESQERSVNMLANAKAVIDRKKAEALEASSAAGVSGSRREQAKKLAGLIPGATVAEWRDYMALLTAPLAQTVRNPQYAERALSAIAQAKADLPPAAELLFQLNAHLFILESLITPGGLHNAGALSSPGYALGYYTAIAVSELQEAIIRLMKRSLPLASEPEAWPRLKDTLAYVQLEMLTESRDRLREQPYFSFCYDQLWQRWIAPNASDPALYLEELEALRDRAGGLGAAVNRSALLLAESRMYFYLSDDKAAWERLAAASERPGLHPDELLGCLEPLAEAGHWSRLAAWLETTGPLLNSRLYNLHSYAGYWEEVVRRLPEAEPRMWSTLSAMLPLSGGIYEDKLLDHGKWRDWMDYQLSSGKVPSDFRVSDLQPVEKHAPELLLPFYHQAAERFVLEKNRHSYKAAVKLLKRLAKLYKKMKREERWGEFLDAFTTRHSRLRALQEELRKGKLIP
>NZ_LN831776.1|WP_039790964.1|411576_413892_+|AraC-family-transcriptional-regulator
MLRFKLKYLLNNKQNRLILMLTVSVSLLIILIGLFSYREYRNALDTELNTPNIELLQINLDVTNRAFRESDNKAVDLSFHQAVLKYMDADTEDAGFAAGLQDVLKTLVTEPDIHAISVIKFKDHSVISSGYGYKASWEEAPEHAWTPWIGQIKEKPLLIKRRVYTGTDPRLSATELLSLARPIVRNGEVAGAVWIDLDYDMLFSKMYSHLSSYQFVYDLEGELIYPKLNLPFPLAEMDKVLKEIDVSPFAHVKIEGKAYMANQTFSNVTGWRMLSLVPMEQLLKNVTTARNMMLMLSLISIAVGCSAIYYYNFAAFRPLKRINKLLTPDMAAAGQGNLYDLEPVIGKLVGDFQSKSLVADWSLPELRSKYVNDLISRSMGTQEMRTKWEHYFSDWREGSFQLLIISIDRYSQWAASFVEEDQMLLKYAMNNIVLEYFEPAWRVVTTAPQRDSLAVLLQPREQEERELKEEAVRLVVLLQEVLKISVSIGAGSTASGVAQAARSYDESMHALSCRLYEGYSLVHAYPEAESKYTESFGAADEAWRQEVLHALKSSDGETALKRVRRGTGEIRKLGIQPQKVFRSINDLLEEIMSIATAGGYPLPAELADYTWHQVTTMDLAEIEDMLCRIVIHMADVLGAHRQSKEYLLVQNLIAYMESHLQENIGLQDIAAHVNMGVSSVSTIFKEETGSTVYDYLTNLRIDKACGLLQDSGLKIADIALQVGYQNENSFIRAFRKIKSTTPGKFRESSKYASGYADRPKPRRSGVSEDSE
>NZ_LN831776.1|WP_085981682.1|414084_415080_+|tripartite-tricarboxylate-transporter-substrate-binding-protein
MRIGIWTASLLAVVILLFIVSRITDDRSHKGDNADFPGKPITLIVPYAAGGGTDATARALAKAAEKVLGQPVIVVNRTGGGGSVGLMEGAGAKGDGYTVTFLPAELTILPHLGLLPITYEKFKPIAQTNFDPSAITVRQGAPWQTVNEFLGFAKAHPGELKMGNAGTGSIWHLAAITLERETGVKFAHIPFEGAGPAVSALMDGFVDAVPVSPAEVKKYVDEGKLRTLAVNADERSDALPGVPTLEELTGIHVNFTGTWRGLAVPKDTPDAIADILAGAFIKGTEDKAFREYMNVNGLGLLVKDGKAFSRQLKESDDTFAKMIPELGLSRR

Crispr_ID: NZ_LN831776_5

• CRISPR_ID: NZ_LN831776_5
• CRISPR_location: 548553-548732
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 3 spacers

Consensus repeat of NZ_LN831776_5

Consensus_repeat	Method
TTTGTTGTACAGAATGCAGGATTTC	CRISPRCasFinder

spacers of NZ_LN831776_5

>5.1|548578|26|NZ_LN831776|CRISPRCasFinder
TATCGTTTAAGGCGCCAAGAACATTA
>5.2|548629|27|NZ_LN831776|CRISPRCasFinder
AGCCTGTCCAGCCTGTTCAACACTCAC
>5.3|548681|27|NZ_LN831776|CRISPRCasFinder
CACCTAGTTGGCTTAATCAGCACTCAT

CRISPR arrays and Neighbor proteins around NZ_LN831776_5

CRISPR arrays

The CRISPR arrays of NZ_LN831776_5

>merge|NZ_LN831776|5|548553-548732|CRISPRCasFinder
TTTGTTGTACAGAATGCAGGATTTCTATCGTTTAAGGCGCCAAGAACATTATTTGTTGTACAAAATGCAGGATTTCAGCCTGTCCAGCCTGTTCAACACTCACGTTGTTGCATAATGTGCAGGATTTCCACCTAGTTGGCTTAATCAGCACTCATATTGTTGTAAAATGTGCAGAATTAC

>NZ_LN831776|5|5|548553-548732|CRISPRCasFinder
TTTGTTGTACAGAATGCAGGATTTC	TATCGTTTAAGGCGCCAAGAACATTA
TTTGTTGTACAAAATGCAGGATTTC	AGCCTGTCCAGCCTGTTCAACACTCAC
GTTGTTGCATAATGTGCAGGATTTC	CACCTAGTTGGCTTAATCAGCACTCAT
ATTGTTGTAAAATGTGCAGAATTAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_025705674.1|560345_560558_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020430829.1|533783_536045_-|TPM-domain-containing-protein	unknown	unknown	gnl|CDD|377378
NZ_LN831776.1|WP_020425847.1|548746_549178_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020430824.1|541583_543008_+|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|225307
NZ_LN831776.1|WP_046501039.1|549994_551287_-|2-oxoglutarate-dehydrogenase-complex-dihydrolipoyllysine-residue-succinyltransferase	unknown	unknown	gnl|CDD|235571
NZ_LN831776.1|WP_141639064.1|554802_554925_+|DNA-binding-anti-repressor-SinI	unknown	unknown	gnl|CDD|370051
NZ_LN831776.1|WP_020430828.1|536199_536343_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425845.1|546108_546837_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225818
NZ_LN831776.1|WP_020427230.1|556300_556888_-|signal-peptidase-I	unknown	unknown	gnl|CDD|131283
NZ_LN831776.1|WP_020427231.1|555606_556215_-|hypothetical-protein	unknown	unknown	gnl|CDD|372085
NZ_LN831776.1|WP_046501041.1|551337_554208_-|2-oxoglutarate-dehydrogenase-E1-component	unknown	unknown	gnl|CDD|236499
NZ_LN831776.1|WP_039785219.1|544468_546112_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225814
NZ_LN831776.1|WP_020427232.1|555018_555363_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|238045
NZ_LN831776.1|WP_020425846.1|546961_548236_+|OFA-family-MFS-transporter	unknown	unknown	gnl|CDD|340911
NZ_LN831776.1|WP_020430825.1|539828_540923_-|GGDEF-domain-containing-protein	unknown	unknown	gnl|CDD|143635
NZ_LN831776.1|WP_020430827.1|536593_539728_+|EAL-domain-containing-protein	unknown	unknown	gnl|CDD|236645
NZ_LN831776.1|WP_020427228.1|559316_560294_-|aldo/keto-reductase	unknown	unknown	gnl|CDD|381318
NZ_LN831776.1|WP_081487078.1|543669_544194_-|nucleotidyltransferase-family-protein	unknown	unknown	gnl|CDD|377593
NZ_LN831776.1|WP_039790235.1|532223_533408_-|acetyl-CoA-C-acetyltransferase	unknown	unknown	gnl|CDD|180261
NZ_LN831776.1|WP_020425848.1|549189_549351_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020430829.1|533783_536045_-|TPM-domain-containing-protein	gnl|CDD|377378	pfam04536, TPM_phosphatase, TPM domain. This family was first named TPM domain after its founding proteins: TLP18.3, Psb32 and MOLO-1. In Arabidopsis, this domain is called the thylakoid acid phosphatase -TAP - domain and has a Rossmann-like fold. In plants, the family resides in the thylakoid lumen attached to the outer membrane of the chloroplast/plastid. It is active in the photosystem II.	3.74148e-15
NZ_LN831776.1|WP_020427228.1|559316_560294_-|aldo/keto-reductase	gnl|CDD|381318	cd19092, AKR_BsYcsN_EcYdhF-like, Bacillus subtilis YcsN, Escherichia coli YdhF and similar proteins. Bacillus subtilis YcsN and Escherichia coli YdhF are prototypes of this family. They are uncharacterized aldo/keto reductase family oxidoreductases.	2.25322e-138
NZ_LN831776.1|WP_046501041.1|551337_554208_-|2-oxoglutarate-dehydrogenase-E1-component	gnl|CDD|236499	PRK09404, sucA, 2-oxoglutarate dehydrogenase E1 component; Reviewed.	0
NZ_LN831776.1|WP_046501039.1|549994_551287_-|2-oxoglutarate-dehydrogenase-complex-dihydrolipoyllysine-residue-succinyltransferase	gnl|CDD|235571	PRK05704, PRK05704, 2-oxoglutarate dehydrogenase complex dihydrolipoyllysine-residue succinyltransferase.	0
NZ_LN831776.1|WP_141639064.1|554802_554925_+|DNA-binding-anti-repressor-SinI	gnl|CDD|370051	pfam08671, SinI, Anti-repressor SinI. SinR is a pleiotropic regulator of several late growth processes. It is a tetrameric DNA binding protein whose activity is down-regulated thorough the formation of a SinI:SinR protein complex. When complexed with SinI, the SinR tetramer is disrupted such that is no longer able to bind DNA.	2.94186e-05
NZ_LN831776.1|WP_020425845.1|546108_546837_+|response-regulator-transcription-factor	gnl|CDD|225818	COG3279, LytT, Response regulator of the LytR/AlgR family [Transcription / Signal transduction mechanisms].	7.11881e-65
NZ_LN831776.1|WP_020427230.1|556300_556888_-|signal-peptidase-I	gnl|CDD|131283	TIGR02228, Signal_peptidase_I_W, signal peptidase I, archaeal type. This model represents signal peptidase I from most archaea, a subunit of the eukaryotic endoplasmic reticulum signal peptidase I complex, and an apparent signal peptidase I from a small number of bacteria. It is related to but does not overlap in hits with TIGR02227, the bacterial and mitochondrial signal peptidase I.	6.78517e-38
NZ_LN831776.1|WP_020427231.1|555606_556215_-|hypothetical-protein	gnl|CDD|372085	pfam12389, Peptidase_M73, Camelysin metallo-endopeptidase.	1.35368e-82
NZ_LN831776.1|WP_039785219.1|544468_546112_+|sensor-histidine-kinase	gnl|CDD|225814	COG3275, LytS, Putative regulator of cell autolysis [Signal transduction mechanisms].	0
NZ_LN831776.1|WP_020425846.1|546961_548236_+|OFA-family-MFS-transporter	gnl|CDD|340911	cd17353, MFS_OFA_like, Oxalate:formate antiporter (OFA) and similar proteins of the Major Facilitator Superfamily of transporters. This subfamily is composed of Oxalobacter formigenes oxalate:formate antiporter (OFA or OxlT) and similar proteins. O. formigenes, a commensal found in the gut of animals and humans, plays an important role in clearing dietary oxalate from the intestinal tract, which is carried out by OFA/OxlT, an anion transporter that facilitates the exchange of divalent oxalate with monovalent formate, the product of oxalate decarboxylation. This exchange generates an electrochemical proton gradient and is the source of energy for ATP synthesis in this cell. The OFA-like subfamily belongs to the Monocarboxylate transporter -like (MCT-like) family of the Major Facilitator Superfamily (MFS) of membrane transport proteins. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.50783e-107
NZ_LN831776.1|WP_020430825.1|539828_540923_-|GGDEF-domain-containing-protein	gnl|CDD|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	2.97979e-50
NZ_LN831776.1|WP_020430824.1|541583_543008_+|NAD(P)/FAD-dependent-oxidoreductase	gnl|CDD|225307	COG2509, COG2509, Uncharacterized FAD-dependent dehydrogenases [General function prediction only].	0
NZ_LN831776.1|WP_081487078.1|543669_544194_-|nucleotidyltransferase-family-protein	gnl|CDD|377593	pfam06042, NTP_transf_6, Nucleotidyltransferase. This family consists of several hypothetical bacterial proteins of unknown function. This family was recently identified as belonging to the nucleotidyltransferase superfamily.	3.43756e-76
NZ_LN831776.1|WP_020430827.1|536593_539728_+|EAL-domain-containing-protein	gnl|CDD|236645	PRK10060, PRK10060, cyclic di-GMP phosphodiesterase.	5.51497e-103
NZ_LN831776.1|WP_039790235.1|532223_533408_-|acetyl-CoA-C-acetyltransferase	gnl|CDD|180261	PRK05790, PRK05790, putative acyltransferase; Provisional.	0
NZ_LN831776.1|WP_020427232.1|555018_555363_-|helix-turn-helix-domain-containing-protein	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	4.81227e-14

Protein sequences

>NZ_LN831776.1|WP_020425846.1|546961_548236_+|OFA-family-MFS-transporter
MTTIAGSKRWLIVLGTVIMQMGLGTIYTWSLFNAQLVSKFGWELSSVSITFSITSFALAFATLFAGKLQDRLGLRRLTAAAGIMLGLGLIFSSQARSLPMLYLLAGVVVGYADGTAYITSLSNLIKWFPKNKGLISGVSVGAYGTGSLLFKYINGSLIDSAGVSNAFLYWGLMVMAMIVIGSMLVREAPVAVQVQAAPGSAAPSTAGVSGAAVSAAAKDYTVKEMLRTKEAYLLFVVFFTACMSGLYLIGVVKDIGVQLAGLNIATAANAVAMIAIFNTAGRLILGALSDRMSRLKLVSATLLVTAIATLTLSYATLSYGLFFTCVAAIAFCFGGNITVFPAIVGDFFGLANHSKNYGIVYQGFGIGALSGSFVAAFLGGFKPTFTVIGLLCILACILAVSLKPPVQKQAREKGISLKPSRRTA
>NZ_LN831776.1|WP_020425845.1|546108_546837_+|response-regulator-transcription-factor
MRAIIVEDEVLARQELAFLIGANSAIRIAGEFEDGLDALKYLQTEEVDVIFLDINIPSIDGVLLAQNISRFSVKPYIVFITAYKEHAAEAFEIEAFDYILKPYSETRIKAMLHKLEVAFAARGHQGEEEHVKLSDKVNLWKNEKIIVVDADEIYYASAQEKTTSVITKGEEYNMALSISEFHSRLPQDRFFRCHRSYLVNLSKIKEIIPWFNNTYLLRLRDLDFEVPVSRSKVKEFRQIMRI
>NZ_LN831776.1|WP_039785219.1|544468_546112_+|sensor-histidine-kinase
MLLQLFERAALLLMCLFVLTRVPRFKEIFVQGAYAPQELAMVTVIFSLFAIFGTYTGINVEGSLVNVRIIAIVAGGILFGPWVGLITGVISGVHRFLIDIGGITSVPCLITSIAAGMVSGVIYRRTSAEHRWIAGILAGMACEALTMVLILVMANPASLGVDIVSKIAFPMIAGQISVGLIVLLVQSVEGEKERIAAKQSKLALDIANKTLPYFRSITPQSLRIICGIIKEDIGADAVAITDTRYIRAYVGVGEEYYAETNEIISEETKMTLRSGEITIRDDDTEYMNRAIRSLIIIPLKEKGEVTGALKIYYTKAHKITYSLQAMAVGLSQIISTLMEVSRVEDIKEMANKAELKALQTSINPHFLFNALNAIISSIRIDPDKARELIVNLSGYMRYNLELTDEFIDIRRELQQVQQYVEIEKARFGSRLAVEYEIDELEVRIPSLIIQPLVENAIVHGILKVRGQGTVTISVKDLGSAVRIGITDTGIGISEETIGKVYSGNMPDHKIGLYNVHQRVKLIYGKGLTIHRLDQGTEIYFDVTKEQR
>NZ_LN831776.1|WP_081487078.1|543669_544194_-|nucleotidyltransferase-family-protein
MMNILAAVRDLHLPDSWVCAGFVRSKVWDVQHGFTERTPLGDVDVIYYDPDDIREEVEKSWEAQLRSTAPSVPWSVKNQARMHTVNGLAPYSSSTDGMSKFPETATALGLAMDEYGELRLAAPHGVSDALELTVRPSPHFRANSQLHPIYEARVAGKNWQAVWDQLQVLSVREN
>NZ_LN831776.1|WP_020430824.1|541583_543008_+|NAD(P)/FAD-dependent-oxidoreductase
MSKYDVIVVGAGPAGIFACYELTRKAPELKVLLVDKGHDIYRRNCPILEEKIKLCPPASGRKEFAGCLPACSITAGFGGAGAYSDGKFNITTEFGGWMTDYLAPSKVLELIQYVDAINLEHGATPVITDPTTESIRGIEQRGYAAGLKLLRAQVRHLGTEQNLEILKSIYEYLRVRIDMLFKTEVQDIVTVKEEGKHRVTGITLKNGESYAADKVMIAPGRDGSAWLTDVLKKRRLKMYNNQVDVGVRVETSDVVMREINEHLYEGKFIFNTSVGTRVRTFCSNPSGHVVVENHSGVMAANGHSYKDPALGSMNTNFALLVSHTFTEPFDKPNEYAREICKRANDLSSGGVIVQKYGDILRGRRSTETRIKEGFLEPTLKEAVPGDLGLVLPYNTMKSLIEMVEALEKVTPGIASEHTLFYGVEAKFYSARPKLTENLETEISGLYCGGDGAGITRGLAQAGAAGVWIARGMLG
>NZ_LN831776.1|WP_020430825.1|539828_540923_-|GGDEF-domain-containing-protein
MHIPPPAPRQTYWNRMILNAFWLVLLVHLLTQTVISLSMQGDDPRLSGKSYLFGNVLLPDIMILGTLLVLEAIYKWRPLLSEISNVAASHLIAIVMILNLSDVFYVKPLIMLIPLLVSMLYLRSTYLKATSILCVTYMILLLLDTSVYDNSLRIQNMIIAFILTGTALAGFALIARGRDLMQSLESSLKSEQDLRIQNIIMDRLSKVDPLTELYNHKTFHEYLGWLIEHQQSNPFPMQLAVLDIDNFKKVNDQYGHWVGDIVLRQVAGIVLKHIGADDFAARYGGEEFVVILTAKPLEDSRRIMTQILHGIAALPVAEMDGNSVTVSIGMHDYAGTDSKSSTFQQADDALYEAKKTGKNKIVVV
>NZ_LN831776.1|WP_020430827.1|536593_539728_+|EAL-domain-containing-protein
MKRCQLLLLISIVFMLAPPASAHAERQEIRYQAELGYPPYKYLQNGYLTGFDIDLTSMIFEKQSYLIHYSTGEWEGTYKRLTRGEIDTTGLMAVTEERKKDTLFSKPVFKSYISVYSRQALQEEIKLSTLKNYKVGVGKKQYSETVLRNQTDVSQYIQYATVPQALEALKKGEIDLLFENQEVVDYLIVEQGLTGNIVRRLSNLYPQDVAYGISKSEPQLVTYINARLDRLQQSGAFEELYQQYFFTHSENYTSMIRGRVISGIVIGLFLLVTVIAALRIYIRHLRRTIHSEQAFFRDVIEHSGMIVWAVHADKRIIRFNQYAASMTGLKEKDVLGANLDEIPGLSGGAAALRELLVRAVYQDYVSNVELKLPDHSPEARYFSFRTALIQGMDTQAEDIFVLVGMDVEECKQNELKLQHSYQELEATYEELAATEEELQEQFNKLEASERRFRLASEGSGAYMWELDWESGMYNLSERWYEVMGYTKEEINSFEDGVLSIIHPDDQEPARQARQEHLAGLTPIYEIEYRMRTKDNRYVWFEVRGKAIVDPKDKIVLFLGSLIDISKRKQAEFQLGNSYQELEATYEQLTATQEELVGQYDMLLENQKNMHRLAYMDSLSSLPNRILLLDTMESYFHRPGGKAALLFVDTDNFKYINDTLGHKSGDILIRQASERLQSVMREGDMLSRLGGDEFVVFIKDVEDRAEVLNLAESILRSFRRSFLIGESNLYISVSIGISFYPEDGETTEEILMNADVAMYRAKEEGKNTFVVYDKSMHMSFNERMNIEKHLRSAMNNNEFELHYQPQVEIKTGLITGFEALIRWNSPVLGFVSPLSFIKIAEDSRLIIYIGEWVLREASAFMKSMNDRTGLPYKISVNISIIQLLQDDFVDIVLDSLEESGLAPNCLELEITESIFMESFENTVSKLEFLKSRGIRIALDDFGTGYSSLSYLQQLPISTLKMDKIFIDSLADQGYSQSFVQTIIILGHKMGLDVVAEGVEDADQLAFLKEADCDKVQGYLISRPVPQRGVIELLEPQRRHGPGYSQ
>NZ_LN831776.1|WP_020430828.1|536199_536343_-|hypothetical-protein
MNAATTRTALKVDDYLDLLNLAVKVGDLKWQKEIKSRLQYILCLETR
>NZ_LN831776.1|WP_020430829.1|533783_536045_-|TPM-domain-containing-protein
MKKTFVLFLMFSLLWMPDMYAAGIPARQGIVTDEASLLTKQETAAIAAIAEGDRYTIQVLTVDSLDGAESGAYATDVYDSWDLTPRDVLLLISAGDQKVELNFNNPGLQGYINSWSQAQGGALDTAAITGLLDTYFNPYAREGDFAGGIRSMIQKLHSFGGTGSGATSGGGTVGTTDSGAAGRSSSSPGLLKMAGIVIGIALLAFMLYVLFTGLRRRGQLRSQQEQLAGLLVRANRALESLQPFQGIVQGKTGEMVEGISKRLSAQLVEISALQSSQSSQPPFYRLKALRAASSQLQQTETAFRSTLEEEEQRIAVISDADRNVKQQITELKKEAPELNLQLQSAVKETGYELQEIAGDLKELAEETAKADELELFDPIAAQDMTGEAQEKQAQIEQDLQDVDTYDDKLNGFPGILAAARSTIAAVIEQNSLHNMKVKPYENLEQASAAAATLEAPLRSGDMDEVRKIAARMDTLLGDAIAMTERQALIRQNNLRDLDTVRSRWSGLSQRRNELHSRIAEARSRFAEHHLAPLEEVLETAGTELRQGAGEVPQIETWTSDQRGEYDNARNSLDQLLKLQEETARKFDNAGESLDMLSQRLANVTRLLSEGQERVDAAQRRLQSKGIASISQFQLSLLPEYGELEQLLSLRPYNLDELEAAAHAYESQISSFVEEANRLIRQKEEEGRLAQLAILREQQRREEARKRTSSSGGFGGGRSSGGSSWGGGGRSSGGSSWGGGGGKSGGNSSGGSKW
>NZ_LN831776.1|WP_039790235.1|532223_533408_-|acetyl-CoA-C-acetyltransferase
MKKVALVSPLRTAVGSFNNGLSTLSATELGADVMTACLQQSRLEPALIDQIYLGNVLQAGIGQNPARQAALKAGIPIDVPASTINTVCGSGLHAVALAYNSILAEQGSVLLAGGMESMSNAPYVLKNARNGYKLGNGELIDSVVADGLTCPINKYHMGITAENIAAKYNISRLEQDEFAYGSQIKAREAKNKQVFAEQIVPVLTKTKKAEIWFSEDEHVRADTSKEKLSNLKPVFKENGSVTAGNASGINDGAAAVLVMSEDKCKEHAVQPLAYIKGYSLVGVDPAYMGMGPVKAISSLLREQGIPLEAIDLFEINEAFAAQALAVLKELGINPEKVNVNGGAIAIGHPVGASGARILVTLVHEMVRRSSRYGIASLCIGTGMGIAMLVENALI
>NZ_LN831776.1|WP_020425847.1|548746_549178_+|hypothetical-protein
MAAYYPYEWKLMDFAKSGEQIAYYFRGEPLSERSGSLLQFAYKEQRITDYSAYPRYPTKAELDSSPFYRQTLSELIDEAKQDQKRNLLFMKAVPWTEAVGVQAKYTRQGAFIDLSATLLHGGEVQVYQEPGNKPEKLKVEGGI
>NZ_LN831776.1|WP_020425848.1|549189_549351_+|hypothetical-protein
MDRPDIKPGFSYHYLNWYNEAQDAYYTLTTHGDRILTKEQLLKLAGELMKGGL
>NZ_LN831776.1|WP_046501039.1|549994_551287_-|2-oxoglutarate-dehydrogenase-complex-dihydrolipoyllysine-residue-succinyltransferase
MSEIKVPDLGESISEGTIYKWLVKEGDTVGQGDVLAELETDKVNLEISAEEDGVISSLLRQAGENVAVGETIGIIGSGAGTAGAAAPQAADGGQPEAAAVGSNAPAAAAPVVPAAPEGAAAGTAALASPGARKLARERGIDLGEVSARDPIGRIAAADVKDHGAARPEAAAPSAPPAAVKPAPAKPAAAGSAPQEDGKAVERKRMSRRRLTIASRLVEAQQTAAMLTTFNEVDMTAILDLRKRRKDAFKEKHDVGLGFMSFFTKAVIGALKAYPLLNAEIDGEDLLIKKYYDIGIAVSAKEGLVVPVVRDADRLSFPEIERRIGELASKARANTLSLPELQGGTFTITNGGVFGSLMSTPILNTPQVGILGMHKIQLRPIALDEERTVNRPMMYIALSYDHRIVDGSEAVSFLVKVKELLEDPEALLLEG
>NZ_LN831776.1|WP_046501041.1|551337_554208_-|2-oxoglutarate-dehydrogenase-E1-component
MAVKEPYNESIWSKYHGPNLGYIQEKYEQFVKDPSSVEHHYRDLFTVSGPPPLAPDAVPAPQPALSGGTEWLRKAVRASKLIANIRIYGHMAANIDPLEQGNNPMAKWLDYETYDLTREDLIAMPASLIWENAPADVHTAWDAVHRMLQAYTQTIAYEFGHVHDEQELRWLNSQAESTSSPAPLNNAERKELLNRLIQVEQFETFLHKTFVGQKRFSLEGNDALVPMLDEIVRAAAHDGAEHILMGMAHRGRLNVLAHILGKPYDIIFSEFHHSPNKELFPSEGSMGINYGWTGDVKYHLGADRAVREGETVRTRITLANNPSHLEFVNPVVEGFARAAQEDRNSPGLPQLDTNKAMAVLMHGDAAFPGEGIVAETLNIGKLKGYSNGGTVHIIVNNRIGFTTESEDSRSTHYASDLAKGYEIPIVHVNADDPEACIAAVRLASAYRSQFKKDFVIDLIGYRRHGHNEMDDPETTQPIVYSKVRNHPTVYRVYAERLQRDNIIKADDVKQMNLEAEKVLQQAYDLMKDGKHKNGETKTSVPVQSEASQPQSTAVQLEQLQRINRELLTVPDGFKVYPKLERILQRRKDALNDGERIDWALAETLAFATILKDGTPIRLSGQDSQRGTFAHRHLVLHDSETGGLFSPLHQLSDAKASFGVYNSPLSEASVLGYEYGYNVFAPETLVIWEAQYGDFANAAQVIFDQFIAAGRAKWTQRSNLTILLPHGYEGQGPEHSSARLERYLQLSAEENWTVANLSSAAQYFHLLRRQAALCGKSDARPLVIMAPKSLIRNPRSTSSGAELASGEFQPVLPEPLLGGNPGGVKRLVVCSGKVTLDLQTELEAGKDQDWSWLHILRLEQLYPFPERELAAHLSALGSLTEIVWVQEEPKNMGGWSYAEPRLRAIAPQNVKVQYIGRPERSSPASGYADVHTFEQRRIVTEALKLNSQVQAAVPSSR
>NZ_LN831776.1|WP_141639064.1|554802_554925_+|DNA-binding-anti-repressor-SinI
MLTGDLDLEWVYLLMSAKKAGIEADEIRRFLNEKTALQAM
>NZ_LN831776.1|WP_020427232.1|555018_555363_-|helix-turn-helix-domain-containing-protein
MPDNMGSRIHHLRLEKGWSLSELADKADVAKSYLSNVERNIQSNPSIQFIEKIADALQVSIHSLLYGEPSDADESSLDGEWFRLVQEAMASGISKREFKEFLDYQKWRLEQKDQ
>NZ_LN831776.1|WP_020427231.1|555606_556215_-|hypothetical-protein
MGIKKTLGLGIASAALGLSLIGGGTFAYFSDTATSTATFAAGTLDLNSDPSVIVDIQNLKPGDTVTKTFKLKNDGTLDIGSILLKTTTEVTDTLGDNNGVDLSKFIKVKFLKNNDKGTIISPEVVVYETTLDALKGQTPDLVKNTGWDQILTEADGIKAQSSDSFSVKFEFVDTGEAQNYFQKDKLKLTWNFEAKQGPKKDY
>NZ_LN831776.1|WP_020427230.1|556300_556888_-|signal-peptidase-I
MLIKKILSHTLSAVMVLIFVVLAAAVVVSRASGGEPALFGYEIKTVLSGSMEPGIQTGSIVALKPGGDMTRFKKGDVITFMSEDNILITHRIVDASAKNAAGEVVYRTKGDNNDAVDMTPVSSGNVVAEYTGVTVPYIGYAMNFAASKAGSVVLMIVPGLLLLLYALYSSWKALSALEKKNTALPQAPPGTDIQS
>NZ_LN831776.1|WP_020427228.1|559316_560294_-|aldo/keto-reductase
MLKTLPLNKRSIPASRIALGCMGLGGGWDHEPVTAENVKQGHEAVEAALAIGINFFDHADIYTRGKAEKVFGQIFKERPGLRDEIILQSKCGIKLMEPGDRSNVFDFSKEHILNSVDGTLTRLGTEYIDILLLHRPDPLMDPEEVAEALHQLKAAGKVRHFGVSNMSAAQIKLLQAYCDEPFIVNQLHMSLAKISWVDAVISVNREPWKDITFPEGTIEHCRAENIQLQAWGPLAQGIFSGRPLEGQPENIVNTASMVKTLAEEKNTTPEAIVLSWLMTHPAAIQPVIGTVNPGRIAACRDAGKLELSRREWYDLYVSSRGEKLP
>NZ_LN831776.1|WP_025705674.1|560345_560558_-|hypothetical-protein
MDKDNKLQGDKRDHPEQYPTENPSLFDLDESERNVDPIPVEDLNLEKQEEKDKEGTKHRSSSDKKYHTGF

Crispr_ID: NZ_LN831776_6

• CRISPR_ID: NZ_LN831776_6
• CRISPR_location: 557096-557166
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_6

Consensus_repeat	Method
CAGGTGAAGCTTCCGGTGTGGCT	CRISPRCasFinder

spacers of NZ_LN831776_6

>6.1|557119|25|NZ_LN831776|CRISPRCasFinder
TCCGGTGTGGCTATAGGAGTTGGTT

CRISPR arrays and Neighbor proteins around NZ_LN831776_6

CRISPR arrays

The CRISPR arrays of NZ_LN831776_6

>merge|NZ_LN831776|6|557096-557166|CRISPRCasFinder
CAGGAGTAGCTTCAGGTGAAGCTTCCGGTGTGGCTATAGGAGTTGGTTTAAGTGCAGCCTCCGGTGTGCTC

>NZ_LN831776|6|6|557096-557166|CRISPRCasFinder
CAGGAGTAGCTTCAGGTGAAGCT	TCCGGTGTGGCTATAGGAGTTGGTT
TAAGTGCAGCCTCCGGTGTGCTC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_025705674.1|560345_560558_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427226.1|560766_561327_-|PadR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224609
NZ_LN831776.1|WP_020425847.1|548746_549178_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046501041.1|551337_554208_-|2-oxoglutarate-dehydrogenase-E1-component	unknown	unknown	gnl|CDD|236499
NZ_LN831776.1|WP_046501039.1|549994_551287_-|2-oxoglutarate-dehydrogenase-complex-dihydrolipoyllysine-residue-succinyltransferase	unknown	unknown	gnl|CDD|235571
NZ_LN831776.1|WP_141639064.1|554802_554925_+|DNA-binding-anti-repressor-SinI	unknown	unknown	gnl|CDD|370051
NZ_LN831776.1|WP_020425845.1|546108_546837_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225818
NZ_LN831776.1|WP_020427230.1|556300_556888_-|signal-peptidase-I	unknown	unknown	gnl|CDD|131283
NZ_LN831776.1|WP_020427231.1|555606_556215_-|hypothetical-protein	unknown	unknown	gnl|CDD|372085
NZ_LN831776.1|WP_020427222.1|565596_565797_+|heavy-metal-associated-domain-containing-protein	unknown	unknown	gnl|CDD|225328
NZ_LN831776.1|WP_082118064.1|569120_569774_+|RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|274357
NZ_LN831776.1|WP_020427225.1|561333_562854_-|MFS-transporter	unknown	unknown	gnl|CDD|341045
NZ_LN831776.1|WP_020425846.1|546961_548236_+|OFA-family-MFS-transporter	unknown	unknown	gnl|CDD|340911
NZ_LN831776.1|WP_020427232.1|555018_555363_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|238045
NZ_LN831776.1|WP_020426809.1|569734_570910_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427221.1|565909_568363_+|copper-translocating-P-type-ATPase	unknown	unknown	gnl|CDD|319783
NZ_LN831776.1|WP_020427228.1|559316_560294_-|aldo/keto-reductase	unknown	unknown	gnl|CDD|381318
NZ_LN831776.1|WP_020427223.1|565134_565482_+|metal-sensing-transcriptional-repressor	unknown	unknown	gnl|CDD|197387
NZ_LN831776.1|WP_046501044.1|563066_564860_-|diguanylate-cyclase	unknown	unknown	gnl|CDD|225116
NZ_LN831776.1|WP_020425848.1|549189_549351_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020427226.1|560766_561327_-|PadR-family-transcriptional-regulator	gnl|CDD|224609	COG1695, COG1695, Predicted transcriptional regulators [Transcription].	2.95533e-08
NZ_LN831776.1|WP_046501041.1|551337_554208_-|2-oxoglutarate-dehydrogenase-E1-component	gnl|CDD|236499	PRK09404, sucA, 2-oxoglutarate dehydrogenase E1 component; Reviewed.	0
NZ_LN831776.1|WP_046501039.1|549994_551287_-|2-oxoglutarate-dehydrogenase-complex-dihydrolipoyllysine-residue-succinyltransferase	gnl|CDD|235571	PRK05704, PRK05704, 2-oxoglutarate dehydrogenase complex dihydrolipoyllysine-residue succinyltransferase.	0
NZ_LN831776.1|WP_141639064.1|554802_554925_+|DNA-binding-anti-repressor-SinI	gnl|CDD|370051	pfam08671, SinI, Anti-repressor SinI. SinR is a pleiotropic regulator of several late growth processes. It is a tetrameric DNA binding protein whose activity is down-regulated thorough the formation of a SinI:SinR protein complex. When complexed with SinI, the SinR tetramer is disrupted such that is no longer able to bind DNA.	2.94186e-05
NZ_LN831776.1|WP_020425845.1|546108_546837_+|response-regulator-transcription-factor	gnl|CDD|225818	COG3279, LytT, Response regulator of the LytR/AlgR family [Transcription / Signal transduction mechanisms].	7.11881e-65
NZ_LN831776.1|WP_020427230.1|556300_556888_-|signal-peptidase-I	gnl|CDD|131283	TIGR02228, Signal_peptidase_I_W, signal peptidase I, archaeal type. This model represents signal peptidase I from most archaea, a subunit of the eukaryotic endoplasmic reticulum signal peptidase I complex, and an apparent signal peptidase I from a small number of bacteria. It is related to but does not overlap in hits with TIGR02227, the bacterial and mitochondrial signal peptidase I.	6.78517e-38
NZ_LN831776.1|WP_020427231.1|555606_556215_-|hypothetical-protein	gnl|CDD|372085	pfam12389, Peptidase_M73, Camelysin metallo-endopeptidase.	1.35368e-82
NZ_LN831776.1|WP_020427222.1|565596_565797_+|heavy-metal-associated-domain-containing-protein	gnl|CDD|225328	COG2608, CopZ, Copper chaperone [Inorganic ion transport and metabolism].	1.97144e-15
NZ_LN831776.1|WP_082118064.1|569120_569774_+|RNA-polymerase-sigma-factor	gnl|CDD|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	2.59765e-33
NZ_LN831776.1|WP_020427225.1|561333_562854_-|MFS-transporter	gnl|CDD|341045	cd17502, MFS_Azr1_MDR_like, Saccharomyces cerevisiae Azole resistance protein 1 (Azr1p), and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This subfamily is composed of multidrug resistance (MDR) transporters including various Saccharomyces cerevisiae proteins such as azole resistance protein 1 (Azr1p), vacuolar basic amino acid transporter 1 (Vba1p), vacuolar basic amino acid transporter 5 (Vba5p), and Sge1p (also known as Nor1p, 10-N-nonyl acridine orange resistance protein, and crystal violet resistance protein). MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. This subfamily belongs to the Methylenomycin A resistance protein (also called MMR peptide) and similar multidrug resistance (MDR) transporters (MMR-like MDR transporter) family of the Major Facilitator Superfamily (MFS) of transporters. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.03231e-72
NZ_LN831776.1|WP_020425846.1|546961_548236_+|OFA-family-MFS-transporter	gnl|CDD|340911	cd17353, MFS_OFA_like, Oxalate:formate antiporter (OFA) and similar proteins of the Major Facilitator Superfamily of transporters. This subfamily is composed of Oxalobacter formigenes oxalate:formate antiporter (OFA or OxlT) and similar proteins. O. formigenes, a commensal found in the gut of animals and humans, plays an important role in clearing dietary oxalate from the intestinal tract, which is carried out by OFA/OxlT, an anion transporter that facilitates the exchange of divalent oxalate with monovalent formate, the product of oxalate decarboxylation. This exchange generates an electrochemical proton gradient and is the source of energy for ATP synthesis in this cell. The OFA-like subfamily belongs to the Monocarboxylate transporter -like (MCT-like) family of the Major Facilitator Superfamily (MFS) of membrane transport proteins. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.50783e-107
NZ_LN831776.1|WP_020427232.1|555018_555363_-|helix-turn-helix-domain-containing-protein	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	4.81227e-14
NZ_LN831776.1|WP_020427221.1|565909_568363_+|copper-translocating-P-type-ATPase	gnl|CDD|319783	cd02094, P-type_ATPase_Cu-like, P-type heavy metal-transporting ATPase, similar to human copper-transporting ATPases, ATP7A and ATP7B. The mammalian copper-transporting P-type ATPases, ATP7A and ATP7B are key molecules required for the regulation and maintenance of copper homeostasis. Menkes and Wilson diseases are caused by mutation in ATP7A and ATP7B respectively. This subfamily includes other copper-transporting ATPases such as: Bacillus subtilis CopA , Archeaoglobus fulgidus CopA, and Saccharomyces cerevisiae Ccc2p. This subclass of P-type ATPase is also referred to as CPx-type ATPases because their amino acid sequences contain a characteristic CPC or CPH motif associated with a stretch of hydrophobic amino acids and N-terminal ion-binding sequences. This subfamily belongs to the P-type ATPases, a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids, and are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle.	0
NZ_LN831776.1|WP_020427228.1|559316_560294_-|aldo/keto-reductase	gnl|CDD|381318	cd19092, AKR_BsYcsN_EcYdhF-like, Bacillus subtilis YcsN, Escherichia coli YdhF and similar proteins. Bacillus subtilis YcsN and Escherichia coli YdhF are prototypes of this family. They are uncharacterized aldo/keto reductase family oxidoreductases.	2.25322e-138
NZ_LN831776.1|WP_020427223.1|565134_565482_+|metal-sensing-transcriptional-repressor	gnl|CDD|197387	cd10152, SaCsoR-like_DUF156, Staphylococcus aureus copper-sensitive operon repressor (CsoR), and related domains; this family was previously known as part of DUF156. This domain family includes Staphylococcus aureus CsoR (SaCsoR). SaCsoR is Cu(I)-inducible, and regulates the expression of genes involved in copper homeostasis; it represses a genetically unlinked copA-copZ operon. copA encodes a copper efflux P-type ATPase, and copZ, a copper chaperone. This family belongs to a larger superfamily that contains various transcriptional regulators that respond to different stressors such as Cu(I), Ni(I), sulfite, and formaldehyde, and includes Mycobacterium tuberculosis CsoR (MtCsoR), Bacillus subtilis CsoR, and Thermus thermophilus CsoR. The latter three proteins do not belong to this family. CsoRs form homotetramers (dimer of dimers). In MtCsoR, within each dimer, two Cys residues on opposite subunits, along with a His residue, bind the Cu(I) ion (forming a triagonal S2N coordination complex, C-H-C). These residues are conserved in the majority of members of this superfamily, including this family, and a conserved Tyr and a Glu residue that facilitate allosteric regulation of DNA binding for CsoRs are also well conserved.	7.97913e-40
NZ_LN831776.1|WP_046501044.1|563066_564860_-|diguanylate-cyclase	gnl|CDD|225116	COG2206, COG2206, c-di-GMP phosphodiesterase class II (HD-GYP domain) [Signal transduction mechanisms].	8.24243e-53

Protein sequences

>NZ_LN831776.1|WP_020427230.1|556300_556888_-|signal-peptidase-I
MLIKKILSHTLSAVMVLIFVVLAAAVVVSRASGGEPALFGYEIKTVLSGSMEPGIQTGSIVALKPGGDMTRFKKGDVITFMSEDNILITHRIVDASAKNAAGEVVYRTKGDNNDAVDMTPVSSGNVVAEYTGVTVPYIGYAMNFAASKAGSVVLMIVPGLLLLLYALYSSWKALSALEKKNTALPQAPPGTDIQS
>NZ_LN831776.1|WP_020427231.1|555606_556215_-|hypothetical-protein
MGIKKTLGLGIASAALGLSLIGGGTFAYFSDTATSTATFAAGTLDLNSDPSVIVDIQNLKPGDTVTKTFKLKNDGTLDIGSILLKTTTEVTDTLGDNNGVDLSKFIKVKFLKNNDKGTIISPEVVVYETTLDALKGQTPDLVKNTGWDQILTEADGIKAQSSDSFSVKFEFVDTGEAQNYFQKDKLKLTWNFEAKQGPKKDY
>NZ_LN831776.1|WP_020427232.1|555018_555363_-|helix-turn-helix-domain-containing-protein
MPDNMGSRIHHLRLEKGWSLSELADKADVAKSYLSNVERNIQSNPSIQFIEKIADALQVSIHSLLYGEPSDADESSLDGEWFRLVQEAMASGISKREFKEFLDYQKWRLEQKDQ
>NZ_LN831776.1|WP_141639064.1|554802_554925_+|DNA-binding-anti-repressor-SinI
MLTGDLDLEWVYLLMSAKKAGIEADEIRRFLNEKTALQAM
>NZ_LN831776.1|WP_046501041.1|551337_554208_-|2-oxoglutarate-dehydrogenase-E1-component
MAVKEPYNESIWSKYHGPNLGYIQEKYEQFVKDPSSVEHHYRDLFTVSGPPPLAPDAVPAPQPALSGGTEWLRKAVRASKLIANIRIYGHMAANIDPLEQGNNPMAKWLDYETYDLTREDLIAMPASLIWENAPADVHTAWDAVHRMLQAYTQTIAYEFGHVHDEQELRWLNSQAESTSSPAPLNNAERKELLNRLIQVEQFETFLHKTFVGQKRFSLEGNDALVPMLDEIVRAAAHDGAEHILMGMAHRGRLNVLAHILGKPYDIIFSEFHHSPNKELFPSEGSMGINYGWTGDVKYHLGADRAVREGETVRTRITLANNPSHLEFVNPVVEGFARAAQEDRNSPGLPQLDTNKAMAVLMHGDAAFPGEGIVAETLNIGKLKGYSNGGTVHIIVNNRIGFTTESEDSRSTHYASDLAKGYEIPIVHVNADDPEACIAAVRLASAYRSQFKKDFVIDLIGYRRHGHNEMDDPETTQPIVYSKVRNHPTVYRVYAERLQRDNIIKADDVKQMNLEAEKVLQQAYDLMKDGKHKNGETKTSVPVQSEASQPQSTAVQLEQLQRINRELLTVPDGFKVYPKLERILQRRKDALNDGERIDWALAETLAFATILKDGTPIRLSGQDSQRGTFAHRHLVLHDSETGGLFSPLHQLSDAKASFGVYNSPLSEASVLGYEYGYNVFAPETLVIWEAQYGDFANAAQVIFDQFIAAGRAKWTQRSNLTILLPHGYEGQGPEHSSARLERYLQLSAEENWTVANLSSAAQYFHLLRRQAALCGKSDARPLVIMAPKSLIRNPRSTSSGAELASGEFQPVLPEPLLGGNPGGVKRLVVCSGKVTLDLQTELEAGKDQDWSWLHILRLEQLYPFPERELAAHLSALGSLTEIVWVQEEPKNMGGWSYAEPRLRAIAPQNVKVQYIGRPERSSPASGYADVHTFEQRRIVTEALKLNSQVQAAVPSSR
>NZ_LN831776.1|WP_046501039.1|549994_551287_-|2-oxoglutarate-dehydrogenase-complex-dihydrolipoyllysine-residue-succinyltransferase
MSEIKVPDLGESISEGTIYKWLVKEGDTVGQGDVLAELETDKVNLEISAEEDGVISSLLRQAGENVAVGETIGIIGSGAGTAGAAAPQAADGGQPEAAAVGSNAPAAAAPVVPAAPEGAAAGTAALASPGARKLARERGIDLGEVSARDPIGRIAAADVKDHGAARPEAAAPSAPPAAVKPAPAKPAAAGSAPQEDGKAVERKRMSRRRLTIASRLVEAQQTAAMLTTFNEVDMTAILDLRKRRKDAFKEKHDVGLGFMSFFTKAVIGALKAYPLLNAEIDGEDLLIKKYYDIGIAVSAKEGLVVPVVRDADRLSFPEIERRIGELASKARANTLSLPELQGGTFTITNGGVFGSLMSTPILNTPQVGILGMHKIQLRPIALDEERTVNRPMMYIALSYDHRIVDGSEAVSFLVKVKELLEDPEALLLEG
>NZ_LN831776.1|WP_020425848.1|549189_549351_+|hypothetical-protein
MDRPDIKPGFSYHYLNWYNEAQDAYYTLTTHGDRILTKEQLLKLAGELMKGGL
>NZ_LN831776.1|WP_020425847.1|548746_549178_+|hypothetical-protein
MAAYYPYEWKLMDFAKSGEQIAYYFRGEPLSERSGSLLQFAYKEQRITDYSAYPRYPTKAELDSSPFYRQTLSELIDEAKQDQKRNLLFMKAVPWTEAVGVQAKYTRQGAFIDLSATLLHGGEVQVYQEPGNKPEKLKVEGGI
>NZ_LN831776.1|WP_020425846.1|546961_548236_+|OFA-family-MFS-transporter
MTTIAGSKRWLIVLGTVIMQMGLGTIYTWSLFNAQLVSKFGWELSSVSITFSITSFALAFATLFAGKLQDRLGLRRLTAAAGIMLGLGLIFSSQARSLPMLYLLAGVVVGYADGTAYITSLSNLIKWFPKNKGLISGVSVGAYGTGSLLFKYINGSLIDSAGVSNAFLYWGLMVMAMIVIGSMLVREAPVAVQVQAAPGSAAPSTAGVSGAAVSAAAKDYTVKEMLRTKEAYLLFVVFFTACMSGLYLIGVVKDIGVQLAGLNIATAANAVAMIAIFNTAGRLILGALSDRMSRLKLVSATLLVTAIATLTLSYATLSYGLFFTCVAAIAFCFGGNITVFPAIVGDFFGLANHSKNYGIVYQGFGIGALSGSFVAAFLGGFKPTFTVIGLLCILACILAVSLKPPVQKQAREKGISLKPSRRTA
>NZ_LN831776.1|WP_020425845.1|546108_546837_+|response-regulator-transcription-factor
MRAIIVEDEVLARQELAFLIGANSAIRIAGEFEDGLDALKYLQTEEVDVIFLDINIPSIDGVLLAQNISRFSVKPYIVFITAYKEHAAEAFEIEAFDYILKPYSETRIKAMLHKLEVAFAARGHQGEEEHVKLSDKVNLWKNEKIIVVDADEIYYASAQEKTTSVITKGEEYNMALSISEFHSRLPQDRFFRCHRSYLVNLSKIKEIIPWFNNTYLLRLRDLDFEVPVSRSKVKEFRQIMRI
>NZ_LN831776.1|WP_020427228.1|559316_560294_-|aldo/keto-reductase
MLKTLPLNKRSIPASRIALGCMGLGGGWDHEPVTAENVKQGHEAVEAALAIGINFFDHADIYTRGKAEKVFGQIFKERPGLRDEIILQSKCGIKLMEPGDRSNVFDFSKEHILNSVDGTLTRLGTEYIDILLLHRPDPLMDPEEVAEALHQLKAAGKVRHFGVSNMSAAQIKLLQAYCDEPFIVNQLHMSLAKISWVDAVISVNREPWKDITFPEGTIEHCRAENIQLQAWGPLAQGIFSGRPLEGQPENIVNTASMVKTLAEEKNTTPEAIVLSWLMTHPAAIQPVIGTVNPGRIAACRDAGKLELSRREWYDLYVSSRGEKLP
>NZ_LN831776.1|WP_025705674.1|560345_560558_-|hypothetical-protein
MDKDNKLQGDKRDHPEQYPTENPSLFDLDESERNVDPIPVEDLNLEKQEEKDKEGTKHRSSSDKKYHTGF
>NZ_LN831776.1|WP_020427226.1|560766_561327_-|PadR-family-transcriptional-regulator
MSMKMVILGLLLERNMHPYEIKLVMKERTMDRNMKLQMGSLYYAVDKLAQEDHIEAVEVIRSSDRPDKTIYRITDKGKTLFEQLVLQQIKKNDLIFHPFYTTLAFSRHIDPSKVEKLLEERIRETEHQVNYAYQVYEEHIPTVPRSSLHMMYGKYEHSLTELKWLKRLYEDVSARKLNDIGTPLDL
>NZ_LN831776.1|WP_020427225.1|561333_562854_-|MFS-transporter
MHSKESNLKLVVVGLLLGILMSAMDNTIVASAMGTIVSELGGLDKIVWVTSAYMVMVMAGTPIFGKLSDMYGRKRFFIFGLIVFLAGSALCGTATSITQLSIYRAIQGIGGGALMPIAFTIMFDIYPPEKRGKLTGLFGAVFGISSVVGPLLGAYITDYVGWQWVFYINLPIGVIAFILVTLSYKESVTHSKQRIDWGGAFTLVGAVICLMFALELGGNQYAWDSAQIMGLFGGFAVLLIVFLFIERVAPEAVISFSMFRNRLFATSSILALFYGSAFIVATVYIPIYVQGVYGGSATNSGLVLMPMMIGSVIGSQTGGLLTTKTSFRNIMLLSAVCFVAGVFSLSTLAPDTSRLMLNMFMALTGFGVGFSFSVLSMSSIHHFDMRQRGSATSTSTFMRSLGMTLGITIFGIIQRNSFTNGLSDAFGAGADTSSFGDPRAALTPEARAQIPAPVLEKITNALSGSIAHTFLWALVPAVLGFVFVLLMPGDRLTVRSKKQQPADGQR
>NZ_LN831776.1|WP_046501044.1|563066_564860_-|diguanylate-cyclase
MYSFIICLIGLGLFVIYSEGSFLHFSFSAWGWITAMAGAAVILTVFTFQLPPQGNGLSLDSSVYLACIFIFGLSFTLMVLLLSSLVLLLLEWGSTAGKHINNFSIYCIMIASASFIFTALGGMQGPLLSSHLEAYVSAMAVYFILNTLLIGFYYYVVFHKNLYNTLKGMLTDTILAYACTLVLSLVLTILLYHNHMVGLGLFLCLSILISYSFKRLFSMYRDIEERFNRDPRTGLFTHSYFEQALEEEMSSSKISGTALSLAMIDIDDFKKYNDHFGHLKGDGLIVFLAELLKRETENTNIIVSRYGGEEFTLLMPGYDAAAARNFMESLRRTLNHSRFEGSEIFPQGCLAFSAGIAAYQPDVHFKSELVDHADQALYYAKKQGKNLVHTYGSQSLLEQDIDFSQDVRDIEQQLNLFMYKDLETFKHSKRVFRYAMDISELLNLDTLSKRQFTLGALIHDIGKLEIPWGILNKKDKLSLEEWEMVKWHVTWGKEMALTNEKFKDLAPYIELHHERYDGKGYPYGFKGDEIPRLCRMLTIIDSFDAMTTERPYQPTKSFKEAVVELRACAGSQFDPELTELFIRYIEKREVCGSEAAI
>NZ_LN831776.1|WP_020427223.1|565134_565482_+|metal-sensing-transcriptional-repressor
MSTNEKEHAGHSCGDDCHTSAPGVRKSHHSAEFKSGLTTRLNRIEGQIRGVKGMIERDTYCDDVLNQLAAVQAALNSVGKLLLEGHMKSCIIERIEAGEHEVIDELLVTVNKLMK
>NZ_LN831776.1|WP_020427222.1|565596_565797_+|heavy-metal-associated-domain-containing-protein
MSNVTLNVEGMSCGHCVSAVEKAVSGVGAAAKVDLQAKTVAVDYDENKVSLSTIKAAIEDQGYDVV
>NZ_LN831776.1|WP_020427221.1|565909_568363_+|copper-translocating-P-type-ATPase
MEKTAETPLQQTTLQITGMTCSACAARIEKGLSRMEGVSKANVNLALEQATVGYDPAVAGVPQIEEKIRSLGYDTRKESADFDISGMTCAACSARIEKVLGRTPGIAAVNVNLALETAHVEYAPGSIGVSEIMEKVSSIGYKATLKQDRKEQADQRGQEIRHKRNKWIISAILSFPLLWAMAGHFSFTEWIWTPELLMNPWFQLALATPVQFIIGWKFYVGAYKAVRNGSANMDVLVVLGTSAAYFYSLYLTIDSLSMSGMSHTVDMYYETSAVLITLILVGKWSEALAKGRSSDAIRSLMGLQAKTALVVRDGAELSIPVEEVIPGDIVLVKPGTKVPVDGEVVEGLSSVDESMLTGESIPVEKKPGDSVIGGTLNKNGMLRIKARKVGRDTALAQIIRVVEEAQGSKAPIQRIADVISGIFVPIVVGIAAVTFVIWFLWGAPGQFAEALENAIAVLVIACPCALGLATPTSIMAGSGRAAEFGILFKGGEHLEAAQGIQVVVLDKTGTVTSGKPVLTDILTTTGIAAHGKETAENRLLALTAAAEKLSEHPLADAIVAGAAARGLELPEAGEFRAVPGRGITAVVGGQTVSVGTRRMMEEGGAEPGPWAPLMTKLEQEGKTAMLVSVEGVIAGVVAVADTIKETSRAAVAKLHDMGIEVVMITGDNRITAQAIAEQAGIRTVLAEVLPEGKAAEIRRLQSGGVKVAMVGDGINDAPALATADTGMAIGTGTDVAMEAADITLMRGDLMSIPDAVMMSRRTMRNIKQNLFWALAYNTIGIPIAALGFLAPWLAGAAMAFSSVSVVLNALRLQRVKL
>NZ_LN831776.1|WP_082118064.1|569120_569774_+|RNA-polymerase-sigma-factor
MSRFQERRCYIWRRGGRRESVNSIESIETKIARIQAGEVYIFADIIDTYQNRIYKYCLRLLSNREEAEDAVQDIMLKVFEKVRYYQPKGSFTSWLYKVAYNHCLNLLRRRKLQRQVSRLFGREAAAESAELAAEDTMFSEPLASALEMLTVEERNLLILRIFEDKSFEEIGEILGKNMEAVKKRYGRIRHKLKAFMELSEKEEGECTKASTLQKNKI
>NZ_LN831776.1|WP_020426809.1|569734_570910_+|hypothetical-protein
MHKSQHTAEEQNLRSYDASGDAKAIDVRQRVMNIITEKYGNVKADAVPPGAGESSEVMQRIEESPARAVRKRLIFHSRTLAVSVSLLAVLFLGSTYYWYADIHNQTADIPYTVKDYEEIEDPVTQFRIQLKETPVQPGVVQPEEDVKTRKYQEAKKWVEQQLLPGETGVFLVGKDLSANPSTGSAVNPLHYDSYSDFRVKSTEQEDPVLPEPEYVPKGYAFSGGEIIPETDIALLLANPSKTTSGDKSESGVEAYLRLKEEMSVMKAIDLGEGYKLVWKRFHAAGASSVKVSYTTTEGQSINIQATDLLRLGTAQFNTYGMEKYENVVVAGKEMIYMKPLAEGGHKYTQRLVWLDSVQGQGAYYSLSDSKDSPLSRQELINVAASMLHSKK

Crispr_ID: NZ_LN831776_7

• CRISPR_ID: NZ_LN831776_7
• CRISPR_location: 568639-568713
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_7

Consensus_repeat	Method
AAATTAGTTATCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_7

>7.1|568663|27|NZ_LN831776|CRISPRCasFinder
AACCTGCGGAGAACAAGGTGTTTGAGC

CRISPR arrays and Neighbor proteins around NZ_LN831776_7

CRISPR arrays

The CRISPR arrays of NZ_LN831776_7

>merge|NZ_LN831776|7|568639-568713|CRISPRCasFinder
AAATTAGTTATCCTTTTTCCACTTAACCTGCGGAGAACAAGGTGTTTGAGCAAATTAGTTATCCTTTTTCCACTT

>NZ_LN831776|7|7|568639-568713|CRISPRCasFinder
AAATTAGTTATCCTTTTTCCACTT	AACCTGCGGAGAACAAGGTGTTTGAGC
AAATTAGTTATCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020427226.1|560766_561327_-|PadR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224609
NZ_LN831776.1|WP_039786295.1|576501_577239_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|378925
NZ_LN831776.1|WP_025705674.1|560345_560558_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426802.1|577245_578397_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|226951
NZ_LN831776.1|WP_020427221.1|565909_568363_+|copper-translocating-P-type-ATPase	unknown	unknown	gnl|CDD|319783
NZ_LN831776.1|WP_020427230.1|556300_556888_-|signal-peptidase-I	unknown	unknown	gnl|CDD|131283
NZ_LN831776.1|WP_020427231.1|555606_556215_-|hypothetical-protein	unknown	unknown	gnl|CDD|372085
NZ_LN831776.1|WP_020426804.1|575590_576502_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224054
NZ_LN831776.1|WP_020426805.1|574623_575376_+|oxygen-insensitive-NADPH-nitroreductase	unknown	unknown	gnl|CDD|380322
NZ_LN831776.1|WP_046501044.1|563066_564860_-|diguanylate-cyclase	unknown	unknown	gnl|CDD|225116
NZ_LN831776.1|WP_020426808.1|571013_571862_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_082118064.1|569120_569774_+|RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|274357
NZ_LN831776.1|WP_020427225.1|561333_562854_-|MFS-transporter	unknown	unknown	gnl|CDD|341045
NZ_LN831776.1|WP_020426806.1|573200_574544_+|PLP-dependent-aminotransferase-family-protein	unknown	unknown	gnl|CDD|224089
NZ_LN831776.1|WP_020426807.1|572043_572997_-|DMT-family-transporter	unknown	unknown	gnl|CDD|307170
NZ_LN831776.1|WP_020426809.1|569734_570910_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427228.1|559316_560294_-|aldo/keto-reductase	unknown	unknown	gnl|CDD|381318
NZ_LN831776.1|WP_020427223.1|565134_565482_+|metal-sensing-transcriptional-repressor	unknown	unknown	gnl|CDD|197387
NZ_LN831776.1|WP_020427222.1|565596_565797_+|heavy-metal-associated-domain-containing-protein	unknown	unknown	gnl|CDD|225328
NZ_LN831776.1|WP_020426801.1|578393_578996_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225107

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020427226.1|560766_561327_-|PadR-family-transcriptional-regulator	gnl|CDD|224609	COG1695, COG1695, Predicted transcriptional regulators [Transcription].	2.95533e-08
NZ_LN831776.1|WP_039786295.1|576501_577239_+|ABC-transporter-permease	gnl|CDD|378925	pfam12698, ABC2_membrane_3, ABC-2 family transporter protein. This family is related to the ABC-2 membrane transporter family pfam01061.	2.60845e-13
NZ_LN831776.1|WP_020427221.1|565909_568363_+|copper-translocating-P-type-ATPase	gnl|CDD|319783	cd02094, P-type_ATPase_Cu-like, P-type heavy metal-transporting ATPase, similar to human copper-transporting ATPases, ATP7A and ATP7B. The mammalian copper-transporting P-type ATPases, ATP7A and ATP7B are key molecules required for the regulation and maintenance of copper homeostasis. Menkes and Wilson diseases are caused by mutation in ATP7A and ATP7B respectively. This subfamily includes other copper-transporting ATPases such as: Bacillus subtilis CopA , Archeaoglobus fulgidus CopA, and Saccharomyces cerevisiae Ccc2p. This subclass of P-type ATPase is also referred to as CPx-type ATPases because their amino acid sequences contain a characteristic CPC or CPH motif associated with a stretch of hydrophobic amino acids and N-terminal ion-binding sequences. This subfamily belongs to the P-type ATPases, a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids, and are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle.	0
NZ_LN831776.1|WP_020427230.1|556300_556888_-|signal-peptidase-I	gnl|CDD|131283	TIGR02228, Signal_peptidase_I_W, signal peptidase I, archaeal type. This model represents signal peptidase I from most archaea, a subunit of the eukaryotic endoplasmic reticulum signal peptidase I complex, and an apparent signal peptidase I from a small number of bacteria. It is related to but does not overlap in hits with TIGR02227, the bacterial and mitochondrial signal peptidase I.	6.78517e-38
NZ_LN831776.1|WP_020427231.1|555606_556215_-|hypothetical-protein	gnl|CDD|372085	pfam12389, Peptidase_M73, Camelysin metallo-endopeptidase.	1.35368e-82
NZ_LN831776.1|WP_020426804.1|575590_576502_+|ABC-transporter-ATP-binding-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	6.00744e-84
NZ_LN831776.1|WP_046501044.1|563066_564860_-|diguanylate-cyclase	gnl|CDD|225116	COG2206, COG2206, c-di-GMP phosphodiesterase class II (HD-GYP domain) [Signal transduction mechanisms].	8.24243e-53
NZ_LN831776.1|WP_020426802.1|577245_578397_+|sensor-histidine-kinase	gnl|CDD|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	2.86874e-54
NZ_LN831776.1|WP_082118064.1|569120_569774_+|RNA-polymerase-sigma-factor	gnl|CDD|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	2.59765e-33
NZ_LN831776.1|WP_020427225.1|561333_562854_-|MFS-transporter	gnl|CDD|341045	cd17502, MFS_Azr1_MDR_like, Saccharomyces cerevisiae Azole resistance protein 1 (Azr1p), and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This subfamily is composed of multidrug resistance (MDR) transporters including various Saccharomyces cerevisiae proteins such as azole resistance protein 1 (Azr1p), vacuolar basic amino acid transporter 1 (Vba1p), vacuolar basic amino acid transporter 5 (Vba5p), and Sge1p (also known as Nor1p, 10-N-nonyl acridine orange resistance protein, and crystal violet resistance protein). MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. This subfamily belongs to the Methylenomycin A resistance protein (also called MMR peptide) and similar multidrug resistance (MDR) transporters (MMR-like MDR transporter) family of the Major Facilitator Superfamily (MFS) of transporters. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.03231e-72
NZ_LN831776.1|WP_020426806.1|573200_574544_+|PLP-dependent-aminotransferase-family-protein	gnl|CDD|224089	COG1167, ARO8, Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs [Transcription / Amino acid transport and metabolism].	1.54065e-112
NZ_LN831776.1|WP_020426807.1|572043_572997_-|DMT-family-transporter	gnl|CDD|307170	pfam00892, EamA, EamA-like transporter family. This family includes many hypothetical membrane proteins of unknown function. Many of the proteins contain two copies of the aligned region. The family used to be known as DUF6. Members of this family usually carry 5+5 transmembrane domains, and this domain attempts to model five of these.	6.33605e-13
NZ_LN831776.1|WP_020426805.1|574623_575376_+|oxygen-insensitive-NADPH-nitroreductase	gnl|CDD|380322	cd02146, NfsA-like, nitroreductase similar to Escherichia coli NfsA. This family contains NADPH-dependent flavin reductase and oxygen-insensitive nitroreductase. These enzymes are homodimeric flavoproteins that contain one FMN per monomer as a cofactor. Flavin reductase catalyzes the reduction of flavin by using NADPH as an electron donor. Oxygen-insensitive nitroreductase, such as NfsA protein in Escherichia coli, catalyzes reduction of nitrocompounds using NADPH as electron donor.	6.353e-110
NZ_LN831776.1|WP_020427228.1|559316_560294_-|aldo/keto-reductase	gnl|CDD|381318	cd19092, AKR_BsYcsN_EcYdhF-like, Bacillus subtilis YcsN, Escherichia coli YdhF and similar proteins. Bacillus subtilis YcsN and Escherichia coli YdhF are prototypes of this family. They are uncharacterized aldo/keto reductase family oxidoreductases.	2.25322e-138
NZ_LN831776.1|WP_020427223.1|565134_565482_+|metal-sensing-transcriptional-repressor	gnl|CDD|197387	cd10152, SaCsoR-like_DUF156, Staphylococcus aureus copper-sensitive operon repressor (CsoR), and related domains; this family was previously known as part of DUF156. This domain family includes Staphylococcus aureus CsoR (SaCsoR). SaCsoR is Cu(I)-inducible, and regulates the expression of genes involved in copper homeostasis; it represses a genetically unlinked copA-copZ operon. copA encodes a copper efflux P-type ATPase, and copZ, a copper chaperone. This family belongs to a larger superfamily that contains various transcriptional regulators that respond to different stressors such as Cu(I), Ni(I), sulfite, and formaldehyde, and includes Mycobacterium tuberculosis CsoR (MtCsoR), Bacillus subtilis CsoR, and Thermus thermophilus CsoR. The latter three proteins do not belong to this family. CsoRs form homotetramers (dimer of dimers). In MtCsoR, within each dimer, two Cys residues on opposite subunits, along with a His residue, bind the Cu(I) ion (forming a triagonal S2N coordination complex, C-H-C). These residues are conserved in the majority of members of this superfamily, including this family, and a conserved Tyr and a Glu residue that facilitate allosteric regulation of DNA binding for CsoRs are also well conserved.	7.97913e-40
NZ_LN831776.1|WP_020427222.1|565596_565797_+|heavy-metal-associated-domain-containing-protein	gnl|CDD|225328	COG2608, CopZ, Copper chaperone [Inorganic ion transport and metabolism].	1.97144e-15
NZ_LN831776.1|WP_020426801.1|578393_578996_+|response-regulator-transcription-factor	gnl|CDD|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	2.38596e-64

Protein sequences

>NZ_LN831776.1|WP_020427221.1|565909_568363_+|copper-translocating-P-type-ATPase
MEKTAETPLQQTTLQITGMTCSACAARIEKGLSRMEGVSKANVNLALEQATVGYDPAVAGVPQIEEKIRSLGYDTRKESADFDISGMTCAACSARIEKVLGRTPGIAAVNVNLALETAHVEYAPGSIGVSEIMEKVSSIGYKATLKQDRKEQADQRGQEIRHKRNKWIISAILSFPLLWAMAGHFSFTEWIWTPELLMNPWFQLALATPVQFIIGWKFYVGAYKAVRNGSANMDVLVVLGTSAAYFYSLYLTIDSLSMSGMSHTVDMYYETSAVLITLILVGKWSEALAKGRSSDAIRSLMGLQAKTALVVRDGAELSIPVEEVIPGDIVLVKPGTKVPVDGEVVEGLSSVDESMLTGESIPVEKKPGDSVIGGTLNKNGMLRIKARKVGRDTALAQIIRVVEEAQGSKAPIQRIADVISGIFVPIVVGIAAVTFVIWFLWGAPGQFAEALENAIAVLVIACPCALGLATPTSIMAGSGRAAEFGILFKGGEHLEAAQGIQVVVLDKTGTVTSGKPVLTDILTTTGIAAHGKETAENRLLALTAAAEKLSEHPLADAIVAGAAARGLELPEAGEFRAVPGRGITAVVGGQTVSVGTRRMMEEGGAEPGPWAPLMTKLEQEGKTAMLVSVEGVIAGVVAVADTIKETSRAAVAKLHDMGIEVVMITGDNRITAQAIAEQAGIRTVLAEVLPEGKAAEIRRLQSGGVKVAMVGDGINDAPALATADTGMAIGTGTDVAMEAADITLMRGDLMSIPDAVMMSRRTMRNIKQNLFWALAYNTIGIPIAALGFLAPWLAGAAMAFSSVSVVLNALRLQRVKL
>NZ_LN831776.1|WP_020427222.1|565596_565797_+|heavy-metal-associated-domain-containing-protein
MSNVTLNVEGMSCGHCVSAVEKAVSGVGAAAKVDLQAKTVAVDYDENKVSLSTIKAAIEDQGYDVV
>NZ_LN831776.1|WP_020427223.1|565134_565482_+|metal-sensing-transcriptional-repressor
MSTNEKEHAGHSCGDDCHTSAPGVRKSHHSAEFKSGLTTRLNRIEGQIRGVKGMIERDTYCDDVLNQLAAVQAALNSVGKLLLEGHMKSCIIERIEAGEHEVIDELLVTVNKLMK
>NZ_LN831776.1|WP_046501044.1|563066_564860_-|diguanylate-cyclase
MYSFIICLIGLGLFVIYSEGSFLHFSFSAWGWITAMAGAAVILTVFTFQLPPQGNGLSLDSSVYLACIFIFGLSFTLMVLLLSSLVLLLLEWGSTAGKHINNFSIYCIMIASASFIFTALGGMQGPLLSSHLEAYVSAMAVYFILNTLLIGFYYYVVFHKNLYNTLKGMLTDTILAYACTLVLSLVLTILLYHNHMVGLGLFLCLSILISYSFKRLFSMYRDIEERFNRDPRTGLFTHSYFEQALEEEMSSSKISGTALSLAMIDIDDFKKYNDHFGHLKGDGLIVFLAELLKRETENTNIIVSRYGGEEFTLLMPGYDAAAARNFMESLRRTLNHSRFEGSEIFPQGCLAFSAGIAAYQPDVHFKSELVDHADQALYYAKKQGKNLVHTYGSQSLLEQDIDFSQDVRDIEQQLNLFMYKDLETFKHSKRVFRYAMDISELLNLDTLSKRQFTLGALIHDIGKLEIPWGILNKKDKLSLEEWEMVKWHVTWGKEMALTNEKFKDLAPYIELHHERYDGKGYPYGFKGDEIPRLCRMLTIIDSFDAMTTERPYQPTKSFKEAVVELRACAGSQFDPELTELFIRYIEKREVCGSEAAI
>NZ_LN831776.1|WP_020427225.1|561333_562854_-|MFS-transporter
MHSKESNLKLVVVGLLLGILMSAMDNTIVASAMGTIVSELGGLDKIVWVTSAYMVMVMAGTPIFGKLSDMYGRKRFFIFGLIVFLAGSALCGTATSITQLSIYRAIQGIGGGALMPIAFTIMFDIYPPEKRGKLTGLFGAVFGISSVVGPLLGAYITDYVGWQWVFYINLPIGVIAFILVTLSYKESVTHSKQRIDWGGAFTLVGAVICLMFALELGGNQYAWDSAQIMGLFGGFAVLLIVFLFIERVAPEAVISFSMFRNRLFATSSILALFYGSAFIVATVYIPIYVQGVYGGSATNSGLVLMPMMIGSVIGSQTGGLLTTKTSFRNIMLLSAVCFVAGVFSLSTLAPDTSRLMLNMFMALTGFGVGFSFSVLSMSSIHHFDMRQRGSATSTSTFMRSLGMTLGITIFGIIQRNSFTNGLSDAFGAGADTSSFGDPRAALTPEARAQIPAPVLEKITNALSGSIAHTFLWALVPAVLGFVFVLLMPGDRLTVRSKKQQPADGQR
>NZ_LN831776.1|WP_020427226.1|560766_561327_-|PadR-family-transcriptional-regulator
MSMKMVILGLLLERNMHPYEIKLVMKERTMDRNMKLQMGSLYYAVDKLAQEDHIEAVEVIRSSDRPDKTIYRITDKGKTLFEQLVLQQIKKNDLIFHPFYTTLAFSRHIDPSKVEKLLEERIRETEHQVNYAYQVYEEHIPTVPRSSLHMMYGKYEHSLTELKWLKRLYEDVSARKLNDIGTPLDL
>NZ_LN831776.1|WP_025705674.1|560345_560558_-|hypothetical-protein
MDKDNKLQGDKRDHPEQYPTENPSLFDLDESERNVDPIPVEDLNLEKQEEKDKEGTKHRSSSDKKYHTGF
>NZ_LN831776.1|WP_020427228.1|559316_560294_-|aldo/keto-reductase
MLKTLPLNKRSIPASRIALGCMGLGGGWDHEPVTAENVKQGHEAVEAALAIGINFFDHADIYTRGKAEKVFGQIFKERPGLRDEIILQSKCGIKLMEPGDRSNVFDFSKEHILNSVDGTLTRLGTEYIDILLLHRPDPLMDPEEVAEALHQLKAAGKVRHFGVSNMSAAQIKLLQAYCDEPFIVNQLHMSLAKISWVDAVISVNREPWKDITFPEGTIEHCRAENIQLQAWGPLAQGIFSGRPLEGQPENIVNTASMVKTLAEEKNTTPEAIVLSWLMTHPAAIQPVIGTVNPGRIAACRDAGKLELSRREWYDLYVSSRGEKLP
>NZ_LN831776.1|WP_020427230.1|556300_556888_-|signal-peptidase-I
MLIKKILSHTLSAVMVLIFVVLAAAVVVSRASGGEPALFGYEIKTVLSGSMEPGIQTGSIVALKPGGDMTRFKKGDVITFMSEDNILITHRIVDASAKNAAGEVVYRTKGDNNDAVDMTPVSSGNVVAEYTGVTVPYIGYAMNFAASKAGSVVLMIVPGLLLLLYALYSSWKALSALEKKNTALPQAPPGTDIQS
>NZ_LN831776.1|WP_020427231.1|555606_556215_-|hypothetical-protein
MGIKKTLGLGIASAALGLSLIGGGTFAYFSDTATSTATFAAGTLDLNSDPSVIVDIQNLKPGDTVTKTFKLKNDGTLDIGSILLKTTTEVTDTLGDNNGVDLSKFIKVKFLKNNDKGTIISPEVVVYETTLDALKGQTPDLVKNTGWDQILTEADGIKAQSSDSFSVKFEFVDTGEAQNYFQKDKLKLTWNFEAKQGPKKDY
>NZ_LN831776.1|WP_082118064.1|569120_569774_+|RNA-polymerase-sigma-factor
MSRFQERRCYIWRRGGRRESVNSIESIETKIARIQAGEVYIFADIIDTYQNRIYKYCLRLLSNREEAEDAVQDIMLKVFEKVRYYQPKGSFTSWLYKVAYNHCLNLLRRRKLQRQVSRLFGREAAAESAELAAEDTMFSEPLASALEMLTVEERNLLILRIFEDKSFEEIGEILGKNMEAVKKRYGRIRHKLKAFMELSEKEEGECTKASTLQKNKI
>NZ_LN831776.1|WP_020426809.1|569734_570910_+|hypothetical-protein
MHKSQHTAEEQNLRSYDASGDAKAIDVRQRVMNIITEKYGNVKADAVPPGAGESSEVMQRIEESPARAVRKRLIFHSRTLAVSVSLLAVLFLGSTYYWYADIHNQTADIPYTVKDYEEIEDPVTQFRIQLKETPVQPGVVQPEEDVKTRKYQEAKKWVEQQLLPGETGVFLVGKDLSANPSTGSAVNPLHYDSYSDFRVKSTEQEDPVLPEPEYVPKGYAFSGGEIIPETDIALLLANPSKTTSGDKSESGVEAYLRLKEEMSVMKAIDLGEGYKLVWKRFHAAGASSVKVSYTTTEGQSINIQATDLLRLGTAQFNTYGMEKYENVVVAGKEMIYMKPLAEGGHKYTQRLVWLDSVQGQGAYYSLSDSKDSPLSRQELINVAASMLHSKK
>NZ_LN831776.1|WP_020426808.1|571013_571862_+|hypothetical-protein
MRFQKSAIALASLALLLGSAYGSASAASGSKSSTKSAAAASSQQTTKKIQAQVDAIRLQTKKPGEIYYVYVNDKKYNPGGVSYQAFSYGLPFKNYQEYVQKAQVLKTPFLQLEQAPEDFQFKSAYLSAFKPKPDSIEGQKLSEQIVAEGKASGKTVFVKKMTDKRWSVTLTYHGSEGSRQAGAFLSITAEPAGTLDSSIEYVPSLAEPEKLSVEGQDLTYKAGDALKYKTANSPGVNNSQDAQYLEWTDSRTKISYTIYVSKGKITKEALVSLAEQIITGQS
>NZ_LN831776.1|WP_020426807.1|572043_572997_-|DMT-family-transporter
MQQQGLKLAYIFAVLNAVIIGFSFLFTKVALGHAGPLDTLTYRFAASFVVMSVPVAFGWVKVSYRGKPIGRALLLAAMYPLGFFTLQVFGLQHATSAEGGILYSFTPVVTMIIASVFLKETTTLLQKLCIFLSVFGVVFIFVMKGSSIQLSNMTGIVLLFLTCLAFAGYSVLARSLSRHFSPAELSYLLMGIGFATFLILSLTGHAASGTLGGFLSPLKSGTFILSAVYLGVIASLVTTLTSTYILSKIEASLMSVFSNLSTIVSIAAGALFLGEEITVYHWIGSFLIIAGVIGTNRLGRKKTEARPGGDRTVPVSR
>NZ_LN831776.1|WP_020426806.1|573200_574544_+|PLP-dependent-aminotransferase-family-protein
MKKYLEVLSDMEKRIKGGQYSPGQKLPSVRSAAEFYSCSVSTVLRAYGELERTHAIYSVPQSGYYMVEQSEEPGPGGGSGIVDFASASPDLNVFPYLDFQHCLNKAIDRYKYHLFTYGDALGLDTLRHTLVSHLAEYQVFAKVERIIITSGIQQALEILARMPFPNGRTEILVEQPGYDIYLRYLEAEGLPVSGIARSAAGIDLRELEAQFASGRFKFFYTMPRYHNPLGTSYSTEERKAIARLAGKYDVYIVEDDYMADLGAEQRFDPIFAYEQTSHTVYLKSFSKIIFPGLRLGAAVVPEPLLEAFRAYKGYTDTSLLSQAALEVYIKNGMYGHHRHKIKAMYAERIQAVYEALARHNTEGLIEVSAASSGVYLQFKLPVAVNLERLVKRLAERKISVVSGNGFYLSGYRNREKFLRISISRARLDQIDEGVRTIAQEAARGSGW
>NZ_LN831776.1|WP_020426805.1|574623_575376_+|oxygen-insensitive-NADPH-nitroreductase
MKPNNETLELLNRHTSVRQFQDKPVSDEQLAAIIGAGQMASTSSNVQAYTVIAVTEPDLKAQLSKLSGNQAYIEQCPVFLVWCADLYRLREISGPHLQGAASYVGSTENLIVATVDVALAAQNAAVAAESLGLGIVYIGGVRNNIAELSELLGLPELVYPVFGMCLGYPAGVNGIRPRLPLQAVLHHNGYQADASVEQVKVYDEVTRDYMRERTGGQKDTPWSEMMAGRLAQPSRLQMKEFLLQKGFMQK
>NZ_LN831776.1|WP_020426804.1|575590_576502_+|ABC-transporter-ATP-binding-protein
MSHVIEMNRVSKIFNDKKAVDGISFTIGKGSITAVLGPNGAGKTTMLSMLLGLLAPTEGTVKVFGLSPKDVKVRERSGAMLQEVSVMDRLKVREIIALIRSYYPQPMDMEFLVRATGLAPADLNRYAEKLSGGQKRSLAFALALAGNPQLLFLDEPTVGLDTTARRHFWDTVRELAAGGTTILFTTHYLQEAEEIADRILLFSQGTLVADGSPEEIKARMVKQSLSFLPAGDAATLRGQLLKLAPVIDCYDKDGRIHVATENTDEALRAIFTGGLAVKNVRIHQGSLDEAFEQLTRNHEEDMK
>NZ_LN831776.1|WP_039786295.1|576501_577239_+|ABC-transporter-permease
MRLIAMQCKAEMLRIFRNPYYVFWSLLMPILFYFIFTRVVNTGTDDVSKWQAHYLMSMAAFSVMGSAIMTLGIRLVQERTQGWNTFIRITPLPSSVYFAGKMFGQTIMHLFSVLCIFVAGYLINGVALTPGQWVLSGLWILAGSLPFLALGTLVGFMKRADTASGVSNVLYMGLAVAGGMWMPLEILPKVMQRIGHWLPSYNYGEGAWEIVGGGYPQWSNILILLGYLAVFMLLSVYIRKKQEAV
>NZ_LN831776.1|WP_020426802.1|577245_578397_+|sensor-histidine-kinase
MARRQFRLFPQRFGFFPYMWLIYLLFPVINLQEEHGIKLVFGAAMLALFAVTYRQLYWATGRAFTLWLAVQMLIIVILSAAYTPYDLFMGFFTANFIGWYTGEKHYKMAYAVFAAMVLVLLITATWGMALEDLLFLYPFMIIMLVSPFGIRSLHRKRMLEKELDQANEVIKELVKREERMRIARDLHDTLGHTLSLITLKSQLVEKLAAKDAGRTQAEAREIQRISRAALRQVRELVSEMRAVSVAEELAEVGEMLRTADIAMEVEGDAALEGVSDLTQNILSLCIKEAVTNIVKHSGADRCRIALAVTEGEVQISIEDNGVGLHPQEQEGHGRSKGNGMKGMAERLSLIDGSLKLSSGEKGGTVLAVAIPRVVKERKDGVTA
>NZ_LN831776.1|WP_020426801.1|578393_578996_+|response-regulator-transcription-factor
MIRIVIAEDQRLLRGAMASLLDLEDDIEVAGEAGDGAEALAVIERLQPDVCLMDIEMPYKSGLEVAETLKAKGSATKVIILTTFARPGYLERGVKAGIQGYLLKDEPVDKLADAIRRVMDGHREVSPELVFGSLREENPLTDREREILKLAGGGQSAGEIAAVLHLSYGTVRNYISEILNKLEVKSRIEAVRLAEEKGWI

Crispr_ID: NZ_LN831776_8

• CRISPR_ID: NZ_LN831776_8
• CRISPR_location: 670854-670927
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_8

Consensus_repeat	Method
AATTAGTTACCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_8

>8.1|670877|28|NZ_LN831776|CRISPRCasFinder
AACCTGCGGAGAACAGGAGATTCGGGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_8

CRISPR arrays

The CRISPR arrays of NZ_LN831776_8

>merge|NZ_LN831776|8|670854-670927|CRISPRCasFinder
AATTAGTTACCCTTTTTCCACTTAACCTGCGGAGAACAGGAGATTCGGGCAAATTAGTTATCCTTTTTCCACTT

>NZ_LN831776|8|8|670854-670927|CRISPRCasFinder
AATTAGTTACCCTTTTTCCACTT	AACCTGCGGAGAACAGGAGATTCGGGCA
AATTAGTTATCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020425680.1|665907_667893_-|anaerobic-ribonucleoside-triphosphate-reductase	unknown	unknown	gnl|CDD|235937
NZ_LN831776.1|WP_020431575.1|673814_674675_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_020425678.1|668757_669066_+|MTH1187-family-thiamine-binding-protein	unknown	unknown	gnl|CDD|376658
NZ_LN831776.1|WP_020426417.1|659575_660130_+|NADPH-dependent-FMN-reductase	unknown	unknown	gnl|CDD|274653
NZ_LN831776.1|WP_020425685.1|661023_661281_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425682.1|662946_665280_-|ribonucleoside-diphosphate-reductase-subunit-alpha	unknown	unknown	gnl|CDD|181700
NZ_LN831776.1|WP_020431559.1|682257_682680_+|ASCH-domain-containing-protein	unknown	unknown	gnl|CDD|119346
NZ_LN831776.1|WP_020431561.1|681779_682088_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426418.1|657880_659176_-|serine--tRNA-ligase	unknown	unknown	gnl|CDD|235461
NZ_LN831776.1|WP_020426419.1|652001_657599_-|hypothetical-protein	unknown	unknown	gnl|CDD|236505
NZ_LN831776.1|WP_020431563.1|677339_679139_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_020425681.1|665395_665911_-|anaerobic-ribonucleoside-triphosphate-reductase-activating-protein	unknown	unknown	gnl|CDD|274161
NZ_LN831776.1|WP_020425677.1|669102_669876_+|sugar-phosphate-isomerase/epimerase	unknown	unknown	gnl|CDD|224007
NZ_LN831776.1|WP_020431572.1|675853_677368_-|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_020425684.1|661407_662439_-|ribonucleotide-diphosphate-reductase-subunit-beta	unknown	unknown	gnl|CDD|236591
NZ_LN831776.1|WP_020431574.1|674668_675625_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_LN831776.1|WP_063850472.1|672204_673737_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270298
NZ_LN831776.1|WP_020431562.1|679278_681579_-|FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|378963
NZ_LN831776.1|WP_144412084.1|684031_686191_+|choice-of-anchor-A-family-protein	unknown	unknown	gnl|CDD|275059
NZ_LN831776.1|WP_046501083.1|671398_671851_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020425680.1|665907_667893_-|anaerobic-ribonucleoside-triphosphate-reductase	gnl|CDD|235937	PRK07111, PRK07111, anaerobic ribonucleoside triphosphate reductase; Provisional.	0
NZ_LN831776.1|WP_020431575.1|673814_674675_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.1421e-68
NZ_LN831776.1|WP_020425678.1|668757_669066_+|MTH1187-family-thiamine-binding-protein	gnl|CDD|376658	pfam01910, Thiamine_BP, Thiamine-binding protein. The crystal structure of two of these members shows that this domain has a ferredoxin like fold and is likely to exists as at least homodimers. Sulphate ions are are located at the dimer interfaces, which are thought to confer additional stability. Although the function of this domain remains to be identified, its structure suggests a role in protein-protein interactions possibly regulated by the binding of small-molecule ligands. Solution of the structure of the hyperthermophilic anaerobic Thermotoga maritima sequence, UniProtKB:Q9WYV6, shows that this has a beta-alpha-beta-beta-alpha-beta ferredoxin-like fold and assembles as a homotetramer. It was possible to identify a pocket in each monmer that bound an unidentified ligand. It was also found that it bound charged thiamine though not hydroxymethyl pyrimidine. It is proposed that it is transporting charged thiamine around the cytoplasm. Under oxidative conditions this bacterium is under stress, and the transcriiptional unit within which this protein is expressed is up-regulated in these conditions, suggesting that the chelation of cytoplasmic thaimine is part of the response mechanism to such oxidatvie stress, which is mediated by this family.	2.8672e-34
NZ_LN831776.1|WP_020426417.1|659575_660130_+|NADPH-dependent-FMN-reductase	gnl|CDD|274653	TIGR03567, FMN_reductase_NADPH, FMN reductase, SsuE family. Members of this protein family use NAD(P)H to reduce FMN and regenerate FMNH2. Members include the homodimeric, NAD(P)H-dependent enzyme SsuE from Escherichia coli, which serves as a partner to an FMNH2-dependent alkanesulfonate monooxygenase. It is induced by sulfate starvation. The NADH-dependent enzyme MsuE from Pseudomonas aeruginosa is outside the scope of this model (see model TIGR03566). [Central intermediary metabolism, Sulfur metabolism].	2.35672e-69
NZ_LN831776.1|WP_020431572.1|675853_677368_-|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	1.79034e-51
NZ_LN831776.1|WP_020425682.1|662946_665280_-|ribonucleoside-diphosphate-reductase-subunit-alpha	gnl|CDD|181700	PRK09209, PRK09209, ribonucleoside-diphosphate reductase subunit alpha.	0
NZ_LN831776.1|WP_020431559.1|682257_682680_+|ASCH-domain-containing-protein	gnl|CDD|119346	cd06554, ASCH_ASC-1_like, ASC-1 homology domain, ASC-1-like subfamily. The ASCH domain, a small beta-barrel domain found in all three kingdoms of life, resembles the RNA-binding PUA domain and may also interact with RNA. ASCH has been proposed to function as an RNA-binding domain during coactivation, RNA-processing and the regulation of prokaryotic translation. The domain has been named after the ASC-1 protein, the activating signal cointegrator 1 or thyroid hormone receptor interactor protein 4 (TRIP4). ASC-1 is conserved in many eukaryotes and has been suggested to participate in a protein complex that interacts with RNA. It has been shown that ASC-1 mediates the interaction between various transciption factors and the basal transcriptional machinery.	1.06353e-25
NZ_LN831776.1|WP_020426418.1|657880_659176_-|serine--tRNA-ligase	gnl|CDD|235461	PRK05431, PRK05431, seryl-tRNA synthetase; Provisional.	0
NZ_LN831776.1|WP_020426419.1|652001_657599_-|hypothetical-protein	gnl|CDD|236505	PRK09419, PRK09419, multifunctional 2',3'-cyclic-nucleotide 2'-phosphodiesterase/3'-nucleotidase/5'-nucleotidase.	3.34082e-110
NZ_LN831776.1|WP_020431563.1|677339_679139_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	6.19311e-46
NZ_LN831776.1|WP_020425681.1|665395_665911_-|anaerobic-ribonucleoside-triphosphate-reductase-activating-protein	gnl|CDD|274161	TIGR02491, Anaerobic_ribonucleoside-triphosphate_reductase, anaerobic ribonucleoside-triphosphate reductase activating protein. This enzyme is a member of the radical-SAM family (pfam04055) and utilizes S-adenosyl methionine, an iron-sulfur cluster and a reductant (dihydroflavodoxin) to produce a glycine-centered radical in the class III (anaerobic) ribonucleotide triphosphate reductase (NrdD, TIGR02487). The two components form an alpha-2/beta-2 heterodimer. [Purines, pyrimidines, nucleosides, and nucleotides, 2'-Deoxyribonucleotide metabolism, Protein fate, Protein modification and repair].	1.99538e-68
NZ_LN831776.1|WP_020425677.1|669102_669876_+|sugar-phosphate-isomerase/epimerase	gnl|CDD|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	8.0311e-23
NZ_LN831776.1|WP_020425684.1|661407_662439_-|ribonucleotide-diphosphate-reductase-subunit-beta	gnl|CDD|236591	PRK09614, nrdF, ribonucleotide-diphosphate reductase subunit beta; Reviewed.	5.923e-100
NZ_LN831776.1|WP_020431574.1|674668_675625_-|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	5.09569e-117
NZ_LN831776.1|WP_063850472.1|672204_673737_-|extracellular-solute-binding-protein	gnl|CDD|270298	cd13580, PBP2_AlgQ_like_1, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	4.59467e-93
NZ_LN831776.1|WP_020431562.1|679278_681579_-|FAD-dependent-oxidoreductase	gnl|CDD|378963	pfam12831, FAD_oxidored, FAD dependent oxidoreductase. This family of proteins contains FAD dependent oxidoreductases and related proteins.	3.93322e-105
NZ_LN831776.1|WP_144412084.1|684031_686191_+|choice-of-anchor-A-family-protein	gnl|CDD|275059	TIGR04215, conserved_hypothetical_protein, choice-of-anchor A domain. This domain may occur as essentially the full length of a protein, except for an N-terminal sequence and a C-terminal protein-sorting signal such as PEP-CTERM or LPXTG. Most often, the putative surface protein is longer and contains repetitive sequence regions. This is one of very few domains for which both anchoring domains occur, and designated choice-of-anchor A domain. The best characterized member is Bacillus anthracis protein BA0871, a collagen-binding protein with five CNA-family protein B-type repeats toward the C-terminus and an LPXTG cell wall attachment motif.	3.45981e-53

Protein sequences

>NZ_LN831776.1|WP_020425677.1|669102_669876_+|sugar-phosphate-isomerase/epimerase
MAAIKQQIGIQMYTLRDRAEKDFLGTLRKVAEIGYKSVEFAGYFGVSAAELRKTLDELGLSAPSAHVGLDFSSLENMQSALSREIEYAREVGLEYLITPSAPLPEQPALDDVLALIPFFEKASELVRAAGLKYGYHNHDFEFKQVNGQAVIDIWLERIPAEHMVAEFDLGWVHVGGAVPAEYISRYAGRVPLVHIKDFGAGHEEADLGKGQVDFDSVFKAADEAGIQHYIVEQEVFASSSLESARLALDYFRKRGML
>NZ_LN831776.1|WP_020425678.1|668757_669066_+|MTH1187-family-thiamine-binding-protein
MAIGEVTVIPIGTGSTSLSSYVADMQRVLETVEGITYELTSMGTIIEGPLARILAAVEALHESPFTAGAQRVSTSLKIDDRRDKPSTSRSKLESVERKLQAD
>NZ_LN831776.1|WP_020425680.1|665907_667893_-|anaerobic-ribonucleoside-triphosphate-reductase
MTLLEKRYNGGQAAQEVLLEEVIHLGRDIIDSRDLDLLRENANLNGESFSGKMSKFGSEYSKWYARNFTMPPQLVQATLDNVVYVHDLDQYAIGTTNCIFIPFEQLLREGFNTGNGSVRPPNSIMTAMSLVAIIFQSQQNAQYGGVSANKLDFDLAPYVTKSFAKLFRKGLEYFEEGTAGEIGGEVTMSRSDLAEQYPRAFRFALKETESETLQAAESMIHNLNTMSSRSGGQIPFTSINYGTCTSPEGQLVISSLLMATMNGLGSGETPVFPIQIFKCKQGVNQQQGDPNYELFLKAAECSARRLYPNFANLDAPLNLQYYDPADPDTEFATMGCRTRVLGDRFGRNHCSGKGNLSFNTLNLVRLGLAYGIATGRRLAADEEGFYDDLNHYMDIALEGLLHRFRIQASQKAKASDFMMREGVWEGGKALAPEDSVGELLKHGSLSIGFIGMAECMKAMYGKHHGEDMEIHAKALAIVRHMREYCDRKSEELNLNITLFATPAEGLSGKFTKVDRKVIGSIPGVTDREYYTNSFHIPVYYELSAAQKISLEAPFHEYCNAGAISYVELNGNARSNPAAFVKIIRYALEQQVSYFSINHPIDRCSDCGYEGVIGTNCPSCGAHENDVHIRRLRRVTGYLTGDYQTRFNAAKQAEVRDRVKHL
>NZ_LN831776.1|WP_020425681.1|665395_665911_-|anaerobic-ribonucleoside-triphosphate-reductase-activating-protein
MNICGYYPESINEGEGMRAVLFLSGCRHRCPGCFNPKTWNFNYGEPFTLERQREIIAEMAANPLLDGLTLAGGDPFFSAEEAAGFIQELRSVLPDYSVWIYTGYTYEELTAAPGSPEWNLLALCQVVIDGRFVEELKDTTLPYRGSSNQRIIDIQASLAGTEIVHWQPAVL
>NZ_LN831776.1|WP_020425682.1|662946_665280_-|ribonucleoside-diphosphate-reductase-subunit-alpha
MPQLVVKPDNRQLAFDEIRLSVYADRILKGLDHLSKETLLRGVQSKLRREEVSGEEISNAFTMSALELVTKEEPDWKFAAARSLLTSLYKKAAVNRRYKAYPDEPYGELYPLITDLVKKGIYREELLSHYTKEQIEELGGCIDYTRDLLFDYIGLLTLSDRYLAHDFDGRVMELPQERYMIIAMFLMHTEPEEKRLELVKEAYWAMSNIYMTAATPTMSNAGKKVAGQLSSCFIDTVDDSLEGIFDSNTDVARLSKMGGGIGVYLGKVRARGSDIRGHKNTSSGVIPWIRQLNNTAVSVDQLGTRKGAVAVYLDVFHKDILAFLDLKLNNGDERMRAHDVFHGVCLPDLFMEAVEARGHWNLFCPHEVKKVMGWKDAKGRALGLEDFYDEQLGQGSFREKYAEATANLELSRITVPAIDIMKRIMKSQLETGTPYMFYRDTVNRSNPNRHQGMVFSSNLCTEIMQNQSATVIESEELVTKDGQTRIVISKVPGDFVVCNLNSIHLARAIPAGVLERLVPIQVRMLDNVIDINNIEVLQAQYTNSQYRAVGLGTFGLHHLLALEGIRWESDEAVEYNNHLYEHINYLVVRSSMELAREKGRYPKFAGSDWETGAYFTSRGYTSGEQEGKYVTTEQWRELQEQVAADGVRNAWMFAIAPNGSTSIIAGSTASIDPLYELLSYEEKTTYKIANPAPDLSEKTIWYYKTAFLIDQNWSIRMASARQRHVDQGQSFNLYVTPDIKATDFLNLHLNAWKGGLKSTYYVRSRALTIEECESCAS
>NZ_LN831776.1|WP_020425684.1|661407_662439_-|ribonucleotide-diphosphate-reductase-subunit-beta
MQLQKIFNTEAPNQSTRIIDGECSGILNWNDIRMPHMYKLYKVLLLNHWIADEIPMSKDAQQFPLLEAEEQRVFKINIGLLAVLDSMQTMFVGDVKRYFTDSSLEAISAIIGQQEVVHNQSYSYVLSSIVSESEQKEIFEYWKHDPVLLERNQFISDIYQEFRDAPSKETFFRAMVADLILEGIFFYSTFAFFYNLARDQKMMATSQMISYIQRDENQHCYFFAEVFKQLLVDFPELNTKENMDYVYRTIDRAVELETNWGYYTLTNVRGIDMNELSDYIKYTANKRLTLMGLEKAYSGVDVNCMPWIKPFSDEALNATKTDFFEAKSRNYGKVGDDNGFDDL
>NZ_LN831776.1|WP_020425685.1|661023_661281_+|hypothetical-protein
MAVRIFSVIIRVQLGPALISFIAFCAAESPLGVLEINSIAHCAAECGGYASKVPFGENLLHEIQRIAFLCRNWANLLYEIQQIVF
>NZ_LN831776.1|WP_020426417.1|659575_660130_+|NADPH-dependent-FMN-reductase
MAKIVVINGTPSLVSRVNAVIEYAEANLRGRGFEVERINVAELPAEDLIHTKFESEAIVKANGLVAEADAVIVVSPVYKASYTGVLKTFLDLIPEKGLAGKILLPLFMGGSLAHLLTIEYALKPVLSVLGARHILGGVYAVDSQAVRNDQGAVELADELRLRLDSVLAELAEETSHKAARKSAE
>NZ_LN831776.1|WP_020426418.1|657880_659176_-|serine--tRNA-ligase
MLDMNWIRDNEELMRNTAVWKKVDFPLEDLLEWDDKRRELRRETERRRAERNGLTKEVERLLRQGEAAAGEAAKAQVREINAHLTKLEADLTEAEQRCSELLLLAPNPVSADTPIGADDSGNVELRRNGTLPDFGFTARDHVELGELHSIIDIPRGVKAGGPRSYVLKGAGLYLHLAVQRLALDVLAERGFTVMDVPVIVRPEALERTGFFPGGMDQTYELNGEKRWLAGTSEVSLVSLYSDEIVEAEVPLRLAGMSACFRREVGSAGRDVRGLYRVHQFSKIEQVVICKNDPAESEQMLQEILANAEHILQLLELPYRVVAVCSGDMALKTHKQYDIETWMPSRGAYGETHSASNLLDFQARRSGIRFRDKDGRLQYCHTLNNTAVATPRILIPLLENHQQEDGSIYIPKALRKYMDGQEFLHAAVTAAE
>NZ_LN831776.1|WP_020426419.1|652001_657599_-|hypothetical-protein
MNIPSRRTKWWSAALSLVLITDTALPAAPMASAAADNSAPVISQVYGGGGNSGAKYKNDFIELYNPTDTDIDLTGWKVRYASASGSFGDNAKSFTPLSGSVPAGGYFLVQEAAGTGGTDALPAPNLIAEGDAVLSMSGTNGKVELLDASGTRVDLVGYGSASEYEGTPGIEGSGPAPALSNTTAAVRKSSSLLPDGNRGLDTDRNLSDFAVQAPEPRSSGTDSTKAPAVSASIASGQTVPKGTKLSLSTSSVTASVYYSVYVDGSTSAVEDFALYKTPILLQDDTVLIKAYSAEEGKTDSGISQFSYTTKEAISGLTIPKIQGTVQSSTYAGQLVKDVAGIVTYTSGSTFYIQTATPDSDPRTSEAIMVYLPGNKVKAADSVLVDGWVKEYKESGYADATDLLTTEIAATQATVLSSNNPLPAPTVIGTGGRTIPATTISVGLDKELDPAKYALDFYESLEGMRVQLITPKIIGPFDYEIPVTVNNGASTTEVSSPAGGLVLTGADFNPQRILIAAQPGTPVRTGQVFKGNITGVLGYDYGNFKVHPEGALPEVDKGTSIERETTPLKAGADKLTVASFNVENFSLKSGSTKIENIAKAIVTNLNTPDILGLLEVQDNDGDTNSGTVDATDSYKALIDAIKKQGGPTYAFTDIAPVNNMDGGAPGGNIRAGFIYNTERVQLAEGTKGDATTAVAYTKDGGLSLNPGRIDPTNPAFANSRKPLAAEFIFNNKKVMVIANHFNSKTGDSALYGGIQPPVLPSEAQRAEIATVVNGFVSDVLAKSPDANLVVLGDLNDFQFSNTLKILKGSALTNLVDTLPLGERYSYVYQGNSQTLDHMLVNNKLATRSALDIVHINADFDEKEGRVSDHDPLLTQIDFGTENFNLRVLHTNDTHGHLENITKRTSAISSERTGNAVLLDAGDVFSGTLYFTQFKGQADIEFMNNIGYDAMTFGNHEFDLNAKEPEVLKNFVTAAKFPFTSANIDFTTKGSELAELYHDAIGMLETDETKSTAKDGHIYPSVIKDVYGEKVGIFGLTTEDTVGLSSPGEQISFKDHVESAKKTVAMLEAQGINKIIAVTHLGYTVDQELAKAVPGIDIIVGGHSHTKIDNPPAPIVNAGTGKNVLIVQTGEYSQFLGELNVTFDKDGEILAYNGKLLDVNLFGEDSTAKKLLAPYDAKLAIVRNTVVGYSDVDLYTNRMIDGKSVRVVRQEETPIGNMIADSIAEKVRELMPNFVSASDLASIKGVVAIQNGGGIRAAIDKGDITMGEVLTTLPFGNSLAALKVTGAEIISSLENSVSGLSSDQGRFAQVSGMKYTYDSTKKPEIVDSLTGQVTQAGERIVSVEIRQTDGSYLPIDPNAYYLLSTNSFMAGGGDFYRALAGAKADGRYYELGLPDFEVLLSYLKLHHPINSKVEGRITDLKGTTPGPAPTPSTTPTPTATPTPTPTSTSSSGGGGGTPATAAPTPTPGATASALAPPQVTTITAADLTSKLAALPGGTSELVIPLNASSGGAQVVLPGSVLVQQAASNPAAVLTFTVPGGASYSLPLRVLNGTALAAQLGTSDFTVTVSLLQASASTLSSLNQALAAQGGPLTLAAPVMEFTVTAQAGSSSVSLNNFGSTYVKRTLTAPGVLNPQGSTAVSFDPATGKLSFVPSVFTGKPDGTTEVAIKRNSNSFYTVVKSGRTFGDITGHWAKASIDLLASKLIITGTSATAFQPSQMVTRAEFAALITRSLGLASMSSGVTFSDVGANAWYTDAVKTAAAAGLITGYTDGSFKPASPITRQEMAAIMAKAMRYTGKSLNVGPAALAKFSDASVIPAWSREAIAGIAAEGIIQGRPDGSFAPQALATRAEAATMLEKTLKSLQFIN
>NZ_LN831776.1|WP_046501083.1|671398_671851_+|hypothetical-protein
MRNYRIRFSLTGFLLYALQLLPNIIWMLVPPVNDVLTGNSSAYKTLNIIEGLFGVLTVTLMIFLLNKAEGRNRNFYIGLAVLFLAGYYISWIFYYNGVVAPWLLILGIACMPPLYFFFAGLWMKNYVLLVPCAIFGVTHILITCMNYLGA
>NZ_LN831776.1|WP_063850472.1|672204_673737_-|extracellular-solute-binding-protein
MRKKNRVMAWTALAMTVALFSGCGGGSNTPKTAEGDASAKSAAGPVDIEAAEISWGTSLPADDFIKKALDEQVGVNLKLTLVGDQNDYENQMNVRAASGNLPDLLMATSKAHLQKLAQSGSLLDLTPYLDKLPEYTKFVGDEVLKKGILDSKQYALPKTGQSVSYTYWIRKDWLDNLQLQPPATVDELLEVAKAFTTNDPDKNGKNDTFGLTGTNFQTFDPIFGAYGLTNIFDTSQLFVRDGKVVSTFYQPEMKEALTTIKGFLDAGVVDPEIVSNKGTMAIDKAFQGKVGIINTEWAQIMKDDKVAVWKGANPKAEWIQLAPPKGPTGIANANSLNIGASSGLWVIPKKLESEPEKLNKVLELLNYVSTKEGNRLVQYGVENTHYTLEGDTVKITDKGRSDASFTWLYQFTGRPETDYLKSKFSNLAAYIDFEANLPRIQTLDGFVTSPPGYNPADANRFIEEEMIKFVYGKAKIDSYSKFLETLENTFSYKNYLDTAISQLNELGYGK
>NZ_LN831776.1|WP_020431575.1|673814_674675_-|carbohydrate-ABC-transporter-permease
MVNAKSDKLFNTVVYLLLAAVAVVAIFPLLYVISMSLTPYSEVIKNGGFVVIPRSISFEAYQRILADPALGRSMLVTVFVTVTGTAINMILTTMAAYPLSRRNLRGRTFFLLFIVITMLFNGGLIPTYLVVRSLGMLDTLWSLIIPGAIATFNVLIMKSFFENLPEELFESAKIDGAKEFRILWQIVIPLSIPSIMTVGLFYMVGHWNSFFSAILYITDVKLHPLQVVIRNMLLLTQSNELQAEVTVPTAAMQMAAVIAGSLPIIVVYPFIQKHFTKGMLLGAIKG
>NZ_LN831776.1|WP_020431574.1|674668_675625_-|sugar-ABC-transporter-permease
MEESIGMTRNKTAESPLRQAWIRIWGMRALYLMLLPCLIWYFVFKYLPMYGVIISFKDYSFTDGILHSPWADPWYKYFKMFFDSPYFLQLMSNTLLISLYKLVFGMLPSIILAILFHECRVMWLKRWVQTLSYMPHFLSWIIIYGISVAFFSETTGLVNRWITEAGGSSISFLGSTEWFRSMLVSTEIWKDIGWGAIVYLAAISGIDPTLFEAARVDGASRLRMIWHITLPGIRNVIILLLILKIGSIMDAGFEQIYVFYNPRVYEVGDIIDTWVYRTGLEQMNFSLATTVGLFKSAIGFVLVLGANKLAKRWGGGIW
>NZ_LN831776.1|WP_020431572.1|675853_677368_-|response-regulator
MWKILLVEDEPFVRRSIRQSIRWEEHGFSITGEATHGQEALELMDRLQPDIVITDIFMPYMDGLELIQAARAKGFEGSFIMLTCAGEFEYARLALEYGASSYILKLSMSDEELLQALNKARAKLMKRVEQQDRLEDQLFREAAGYMWRSLWGKELHQDETDKFEDFRRRAANSPGLLLISVLGGTRMLSKADLPSLLPAEAGQAARCHLFRYMGQSTFWVWLERSPALRPEVFIYDGLPAVRRLGSAADAGLGAWRMNLEVLGRYYYGCARGENGVTAEADTAPVHPLPVPWEQEREIIGRFERLDVGDCAAKLEQLWQFMAAVRMPMAAVKETAERLDKLFARIAGKPAEPPGALLDAVRHPELLEQTVARMRTYAKGLGGQRPQETDHPEINTMIRYLLHHYDEDISLQAMAQYVNMDENYLSGLFKKKTGETFINYLQHIRVNEARFYLEQTDLTVAEIGERVGFANPSYFFKIFKRWTKLTPNEYRQQCKGKAGTEPPAP
>NZ_LN831776.1|WP_020431563.1|677339_679139_-|sensor-histidine-kinase
MGKLKWLWPSSMKNRLVLSILLFVLIPSAFLQIRNITQLETMMKDNISQQNAAQLNFLKNNIESLKFGVLGAMLQLERDPDLREQLGRTGENMPEKNMFIKNELLLVKQRLMNAIVPVHLTLVDDKGEVYNTLEEGMAVPAVSGAELLQQPEFVKLRQGAEAYYWTVHEPDYLLANALPGSQLFSLFSKLQGTDGHTFAYLRISLDMKTWLNSITGGFQVKQTYYLLDGGGQPILMGRNDRSAQALGGMLATFKSNPARYFTDDKDLFIFNGTYLPNMDWYLVSRFPLEALSGNILAMKREVMLSFLVTCIIFAGIMYAIVSSTVRPLHNLQKKMSELVDKNLNVSIPERKYKGELLRLARAFNLMTGDIRKLIERLQMEERQKEAIRFQMLMSQMNPHFLLNTLNTIKWNARNHGDMGTSEICQNLGKLLESGLNSDADLVFLKEEIELIRAYVYIQSFRYDHSFNVEYMIGDGLEYALIPKFSLQPLVENAIYHGLVHMKAGGKITILIAGAGGRLRVEIGDNGQGLERSGSASGKRRKGIGLSNLRERIMLLYKGRGELLLLPLPQGTVAVLDIPLLNSLPYDKEERNVENTSGRG
>NZ_LN831776.1|WP_020431562.1|679278_681579_-|FAD-dependent-oxidoreductase
MKMRQEVYDVVVCGGGLAGVCAAVAAARQGAGVCIIQDRPVLGGNSSSEIRVTPHGAAQFHAYARETGIISELLIEERALNHEPILENGWTNSVWDMVLYNLAVSTPNLTLHLNSTVTEVHKNAERHISSVTVRVAGAETQIAIEGRVFIDCTGDGVVADLAGCEWRWGSEGREEFSEPHAPLAASGDTMGSSIHFKAKDMGRPVPFAAPDWAVRHEDPAFFYDQGRHFYDLAAGYWWIEIGIPWNTIYDNEHIRHELTRHTLGIWDWIKNRDPLLKEKAANYALDWIGQVPGKRESRRVLGRYFMTEHDPAGRTIFPDEIAYGGWFIDLHSTGGLLAPTAEPSSAEGYAETSEYAIKSYCGPYGIPLRILMSKDIDNLLLAGRNVSVSHAALGTVRVMATTALLGQAAGTAAAVALRQGREACSLDFADIREVQQILLREGCFLPNCRNEDPGDVARSARVQASSSARVHGVGPESRDYTGGFGGTRLPDKEPLTHRRGQWIAAGTEEIRSLAVCLSNESGTEQTIEASLVPVDSIWDYECGAKQPLARQQLAVPPGRMQWVAWEAGLTAADGLRSGGYVRLELAANPQVEWHKGGTVIPGHTSAYEMGPSKMRRYGDGGTLSFRIEPPQACYEPSNVLTGIARPYDYTNMWRSDPAGPLPQRLELEWETEECIGTVELAFPGQLFREYHRYPPFYRDPQCPRDYSIDAWTGVGWTTVASVTGNYQTRRRHPLSEAVKTDKLRVTVHATNGDPSACIAEIRCYRS
>NZ_LN831776.1|WP_020431561.1|681779_682088_+|hypothetical-protein
MSNLRNKYIFIFTFTCFAAFLLLFLQPALVHAADAGTMVDSGTKERLMEQYGLEPPKPSFSMGWTGMDGGMSTPLQVFLAICGLAASPYLVVIWNFILLRFS
>NZ_LN831776.1|WP_020431559.1|682257_682680_+|ASCH-domain-containing-protein
MKCLTIRQPWATLIALGEKQLETRSWQTAYRGELAIHAGMGIDTTACRQEPFKSALARHGFTVDNLPRGAIIATSRLAGCYEVTQAAADEGWPGGNELVFGDYAPGRYAWKLEDVTALARPIPAKGRLSFWEYPVLEGEQ
>NZ_LN831776.1|WP_144412084.1|684031_686191_+|choice-of-anchor-A-family-protein
MKKRSLKAAALILTGVLALSSTVTWGWNVKAAGNMPYIPTPVLGVAGNFNAFIFGDFTQSYDQIHGRLAAEGNITLQGYGVSKDAPGGDVLVAGKNLTLTDGTIYGAAVYGGTISTTRADLKETPRQGTPIDFAAEEQFLVRRSDELAALTQTQPFVKEYGKMTINAPDAYNVIHLAAADLADANGLQFNIAGDATVIINVGGSAVKIPNFQFWGGKPRKVLFNFYEAASVNIGNTTIEGTILAPHASVFYDHAELHGTLIAKAFSGYVQMHHYPYEGSEPPATPTPTPSATATPTPSATATPAPSATATPAPSATATPTPSATATPTPSATVTPTPSATATPTPTPSATPTPSGTATPAPSATATPMPSATATPTPSATVTPTPSATATPTPTPSATPTPSATATPTPSATATPAPSATATPTPSATATPMPSATATPTPSATATPTPSATATPTPSATPTPSATVTPTPSATATPTPTPSATPTPSATATPMPSATPTPSATATPTPSATATPMPSATATPTPSATATPTPTPTSSTTPVPTSSVTPTPTSSALPSATASATPTSSTAPTPTSEVTPAPSTATPTPDTTVIYVPVTFPTPTPSSVIGTIVDDTLINDDPLPLGPVSTVAPVQPTAPIQPTASIEPTPAPAPAPTVTPEPEEIVITDDEIPAGSVDTPDKLPQTGEASPAPYYIAGLGIAGLGLLLSRTARNSGKRKR

Crispr_ID: NZ_LN831776_9

• CRISPR_ID: NZ_LN831776_9
• CRISPR_location: 727111-727249
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_LN831776_9

Consensus_repeat	Method
ATTAGTGGTACAAATTCCACTTAGCA	CRISPRCasFinder

spacers of NZ_LN831776_9

>9.1|727137|36|NZ_LN831776|CRISPRCasFinder
TTGCTGAAAACTGCGGATGGACGCGGTTTTGGCTGA
>9.2|727199|25|NZ_LN831776|CRISPRCasFinder
GTCTCAGCAGCGGGTTTGCAGTAAG

CRISPR arrays and Neighbor proteins around NZ_LN831776_9

CRISPR arrays

The CRISPR arrays of NZ_LN831776_9

>merge|NZ_LN831776|9|727111-727249|CRISPRCasFinder
ATTAGTGGGAAAAAGTACACTTAATTTTGCTGAAAACTGCGGATGGACGCGGTTTTGGCTGAATTAGTGGTACAAATTCCACTTAGCAGTCTCAGCAGCGGGTTTGCAGTAAGATTAGTGGTAGAAATTCCACTTAGCA

>NZ_LN831776|9|9|727111-727249|CRISPRCasFinder
ATTAGTGGGAAAAAGTACACTTAATT	TTGCTGAAAACTGCGGATGGACGCGGTTTTGGCTGA
ATTAGTGGTACAAATTCCACTTAGCA	GTCTCAGCAGCGGGTTTGCAGTAAG
ATTAGTGGTAGAAATTCCACTTAGCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020427301.1|726519_726846_+|cytochrome-c-oxidase-subunit-IV	unknown	unknown	gnl|CDD|131954
NZ_LN831776.1|WP_046506362.1|724045_725884_+|cytochrome-c-oxidase-subunit-I	unknown	unknown	gnl|CDD|238832
NZ_LN831776.1|WP_020427144.1|717116_717893_+|zinc-ribbon-domain-containing-protein	unknown	unknown	gnl|CDD|379090
NZ_LN831776.1|WP_046501106.1|727452_728379_+|cytochrome-c-oxidase-assembly-factor-CtaG	unknown	unknown	gnl|CDD|131784
NZ_LN831776.1|WP_020427298.1|722866_723916_+|cytochrome-c-oxidase-subunit-II	unknown	unknown	gnl|CDD|224537
NZ_LN831776.1|WP_020427307.1|731192_732125_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224054
NZ_LN831776.1|WP_020427300.1|725890_726517_+|cytochrome-(ubi)quinol-oxidase-subunit-III	unknown	unknown	gnl|CDD|239214
NZ_LN831776.1|WP_039835617.1|719182_719776_+|xanthine-phosphoribosyltransferase	unknown	unknown	gnl|CDD|181705
NZ_LN831776.1|WP_052741407.1|735179_735947_+|hypothetical-protein	unknown	unknown	gnl|CDD|367466
NZ_LN831776.1|WP_081487276.1|736036_736273_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_019913840.1|722275_722464_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427306.1|730780_731176_+|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224639
NZ_LN831776.1|WP_020427304.1|728977_729760_-|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|293798
NZ_LN831776.1|WP_039833127.1|732129_733032_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|226631
NZ_LN831776.1|WP_020427297.1|721271_721610_-|hypothetical-protein	unknown	unknown	gnl|CDD|227155
NZ_LN831776.1|WP_046501104.1|720127_721069_-|diacylglycerol-kinase-family-lipid-kinase	unknown	unknown	gnl|CDD|224513
NZ_LN831776.1|WP_020426612.1|733024_734323_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|224582
NZ_LN831776.1|WP_020427305.1|729991_730720_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427146.1|718832_719138_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427303.1|728405_728870_+|DUF420-domain-containing-protein	unknown	unknown	gnl|CDD|377257

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020427301.1|726519_726846_+|cytochrome-c-oxidase-subunit-IV	gnl|CDD|131954	TIGR02908, Cytochrome_c_oxidase_subunit_4B, cytochrome c oxidase, subunit IVB. This model represents a small clade of cytochrome oxidase subunit IV's found in the Bacilli. [Energy metabolism, Electron transport].	1.00758e-15
NZ_LN831776.1|WP_046506362.1|724045_725884_+|cytochrome-c-oxidase-subunit-I	gnl|CDD|238832	cd01662, Ubiquinol_Oxidase_I, Ubiquinol oxidase subunit I. Ubiquinol oxidase, the terminal oxidase in the respiratory chains of aerobic bacteria, is a multi-chain transmembrane protein located in the cell membrane. It catalyzes the reduction of O2 and simultaneously pumps protons across the membrane. The number of subunits in ubiquinol oxidase varies from two to five. Subunit I contains a heme-copper binuclear center (the active site where O2 is reduced to water) formed by a high-spin heme and a copper ion. It also contains a low-spin heme, believed to participate in the transfer of electrons from ubiquinol to the binuclear center. For every reduction of an O2 molecule, eight protons are taken from the inside aqueous compartment and four electrons are taken from ubiquinol on the opposite side of the membrane. The four electrons and four of the protons are used in the reduction of O2; the four remaining protons are pumped across the membrane. This charge separation of four charges contributes to the electrochemical gradient used for ATP synthesis. Two proton channels, the D-pathway and K-pathway, leading to the binuclear center have been identified in subunit I. It is generally believed that the channels contain water molecules that act as 'proton wires' to transfer the protons. A well-defined pathway for the transfer of pumped protons beyond the binuclear center has not been identified. Electrons are believed to be transferred directly from ubiquinol (the electron donor) to the low-spin heme, and directly from the low-spin heme to the binuclear center.	0
NZ_LN831776.1|WP_020427144.1|717116_717893_+|zinc-ribbon-domain-containing-protein	gnl|CDD|379090	pfam13248, zf-ribbon_3, zinc-ribbon domain. This family consists of a single zinc ribbon domain, ie half of a pair as in family DZR. pfam12773.	0.00275727
NZ_LN831776.1|WP_046501106.1|727452_728379_+|cytochrome-c-oxidase-assembly-factor-CtaG	gnl|CDD|131784	TIGR02737, Protein_CtaG, cytochrome c oxidase assembly factor CtaG. Members of this family are the CtaG protein required for assembly of active cytochrome c oxidase of the caa3 type, as in Bacillus subtilis.	2.55635e-95
NZ_LN831776.1|WP_020427298.1|722866_723916_+|cytochrome-c-oxidase-subunit-II	gnl|CDD|224537	COG1622, CyoA, Heme/copper-type cytochrome/quinol oxidases, subunit 2 [Energy production and conversion].	4.32523e-75
NZ_LN831776.1|WP_020427307.1|731192_732125_+|ABC-transporter-ATP-binding-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	2.10728e-58
NZ_LN831776.1|WP_020427300.1|725890_726517_+|cytochrome-(ubi)quinol-oxidase-subunit-III	gnl|CDD|239214	cd02863, Ubiquinol_oxidase_III, Ubiquinol oxidase subunit III subfamily. Ubiquinol oxidase, the terminal oxidase in the respiratory chains of aerobic bacteria, is a multi-chain transmembrane protein located in the cell membrane. It catalyzes the reduction of O2 and simultaneously pumps protons across the membrane. Ubiquinol oxidases feature four subunits in contrast to the 13 subunit bovine cytochrome c oxidase (CcO). Subunits I, II, and III of bovine CcO are encoded within the mitochondrial genome and the remaining 10 subunits are encoded within the nuclear genome. Subunits I, II and III of ubiquinol oxidase are homologous to the corresponding subunits in bovine CcO. Although not required for catalytic activity, subunit III appears to be involved in assembly of the multimer complex.	1.17866e-75
NZ_LN831776.1|WP_039835617.1|719182_719776_+|xanthine-phosphoribosyltransferase	gnl|CDD|181705	PRK09219, PRK09219, xanthine phosphoribosyltransferase; Validated.	3.22884e-114
NZ_LN831776.1|WP_052741407.1|735179_735947_+|hypothetical-protein	gnl|CDD|367466	pfam03370, CBM_21, Carbohydrate/starch-binding module (family 21). This family consists of several eukaryotic proteins that are thought to be involved in the regulation of glycogen metabolism. For instance, the mouse PTG protein has been shown to interact with glycogen synthase, phosphorylase kinase, phosphorylase a: these three enzymes have key roles in the regulation of glycogen metabolism. PTG also binds the catalytic subunit of protein phosphatase 1 (PP1C) and localizes it to glycogen. Subsets of similar interactions have been observed with several other members of this family, such as the yeast PIG1, PIG2, GAC1 and GIP2 proteins. While the precise function of these proteins is not known, they may serve a scaffold function, bringing together the key enzymes in glycogen metabolism. This family is a carbohydrate binding domain.	4.173e-18
NZ_LN831776.1|WP_020427304.1|728977_729760_-|MBL-fold-metallo-hydrolase	gnl|CDD|293798	cd07712, MBLAC2-like_MBL-fold, uncharacterized human metallo-beta-lactamase domain-containing protein 2 and related proteins; MBL-fold metallo hydrolase domain. Includes the MBL-fold metallo hydrolase domain of uncharacterized human MBLAC2 and related proteins. Members of this subgroup belong to the MBL-fold metallo-hydrolase superfamily which is comprised mainly of hydrolytic enzymes which carry out a variety of biological functions.	1.51127e-54
NZ_LN831776.1|WP_020427306.1|730780_731176_+|GntR-family-transcriptional-regulator	gnl|CDD|224639	COG1725, COG1725, Predicted transcriptional regulators [Transcription].	1.76029e-31
NZ_LN831776.1|WP_039833127.1|732129_733032_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|226631	COG4152, COG4152, ABC-type uncharacterized transport system, ATPase component [General function prediction only].	6.76346e-126
NZ_LN831776.1|WP_020427297.1|721271_721610_-|hypothetical-protein	gnl|CDD|227155	COG4818, COG4818, Predicted membrane protein [Function unknown].	2.98592e-26
NZ_LN831776.1|WP_046501104.1|720127_721069_-|diacylglycerol-kinase-family-lipid-kinase	gnl|CDD|224513	COG1597, LCB5, Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase [Lipid metabolism / General function prediction only].	2.48264e-64
NZ_LN831776.1|WP_020426612.1|733024_734323_+|ABC-transporter-permease	gnl|CDD|224582	COG1668, NatB, ABC-type Na+ efflux pump, permease component [Energy production and conversion / Inorganic ion transport and metabolism].	4.35736e-42
NZ_LN831776.1|WP_020427303.1|728405_728870_+|DUF420-domain-containing-protein	gnl|CDD|377257	pfam04238, DUF420, Protein of unknown function (DUF420). Predicted membrane protein with four transmembrane helices.	2.06536e-40

Protein sequences

>NZ_LN831776.1|WP_020427301.1|726519_726846_+|cytochrome-c-oxidase-subunit-IV
MATEQHSASSGAVKHRHRQEGPQRHIVVFAFSVVLTLIAFAAVAAGGVNATFAVILLLVMAVLQVFLQMGFWMHLKDKGHLLPIIFMLGGFFIAGTCIVMALYWVWWD
>NZ_LN831776.1|WP_020427300.1|725890_726517_+|cytochrome-(ubi)quinol-oxidase-subunit-III
MTTAHAESAAGNLPHEPEKATLEGRNKVLAFWLFLGGESVLFGTLFATFLALRNQTNEGPSANDLFHLPLVAAATFLLLVSSLTSVFAIQAMHRGKVAVLRNWLLVTVFLGLCFLVLEIYEFSVYVRHEEFGMTTSAFSSAFYTLVGFHGAHVAFGILWISVLIGQLARKGLTVVTAPKIYVSAMYWHFIDVVWVFIFTVVYLLGKVG
>NZ_LN831776.1|WP_046506362.1|724045_725884_+|cytochrome-c-oxidase-subunit-I
MDWITTVDHKKIAILYLWAGGLFFGIGGLEAILIRIQLIKPMNTFLDAQTFNELITMHGTTMIFLGVMPVIFALMNAVIPLQIGARDVAFPFLNALGFWTFLFGGVLLNLSWIMGGAPDAGWTSYTPLSTTQYSGTHGVDFYTIGLQIAGLGTLIGGINFLATIITMRAPGMSFMRMPMFVWASFITSAIILFAFPAITVGLVLLTFDRILEANFFDTSAGGNSVLWQHIFWIFGHPEVYILILPAFGIISEVIPTFARKRLFGYSSMVFATILIAFLGFMVWAHHMFTTGLGPVANALFSVSTMLIAVPTGIKIFNWLFTMWGGQVRFTSPNLFAVGFIPTFTMGGVTGVMLASAPADFQFHDTYFVVAHFHYVIVGGLVSGLFAGLHYWWPKMFGRMLSETLGKWTFWTFIIGFHLTFFVQHFLGLMGMQRRVFTYLPNQQFDLLNLISTIGAGLMGVGVLIFLTNIFLTSRKPADAPDDPWEDGRTLEWTISSPPPEYNFKQTPLVRGLDAFWKEKTSGHKTMTPAEPVGPIHMPSATILPFLMSVGIFIAGLGFMFSRDDFGNAFMGFLFNNYLVTAIGLVITFGSMLLRSLYDDHGWHIEPEELEGR
>NZ_LN831776.1|WP_020427298.1|722866_723916_+|cytochrome-c-oxidase-subunit-II
MMKTWQAGKRLLPMTAALGLILAGCGREDLSVLRPQGPAAESSFDLMKLSITIMIVVLLIVFSIAAYVLVRFRRKPDQREMPEQVEGSFKLEVLWTVIPLVLVVVLAVPTVKAVFAAGNDHSSDKNAIKVKVTGHQYWWEFEYTDYGVTTAQDLVIPAGKDIAFELSTKDVLHSFWVPSLSGKMDTNPDGTTNRFSFSAPNEGVYRGKCAELCGPSHGFMEFKVKSVSEAAFEKWVNSMKAPAVLPEDPALAEKFKSQCLTCHAVGDMPDLSSAPNLTGIGSRESVAGILLNDDTGVDGAPVLENLKTWLHDTAGVKPGNKMPDPKKDMGLSDEEIDGIAEFLAGYTLD
>NZ_LN831776.1|WP_019913840.1|722275_722464_+|hypothetical-protein
MASKGHNEVKESLREMTRIFRPKDPKKFVKEYVRKYRITGGYEEELTMVVEHELVRMNSSVS
>NZ_LN831776.1|WP_020427297.1|721271_721610_-|hypothetical-protein
MSPIRSSTGIPDHIAAALCYFFPFIGGIVFLALEKRSRFVLFHALQSLIAFGALMVAHVLCGFIPLLGPLAAPIISLCSFAVWLLMIYHALGGRWYRLPWAGDIAERQLRQL
>NZ_LN831776.1|WP_046501104.1|720127_721069_-|diacylglycerol-kinase-family-lipid-kinase
MYLLIINPRSGGGAGGRTWHAVEAMLQARGTAYEALFTQSADSAESQVLHALARREDWRAAIVVGGDGTVHSVLGALRRRGVALAVIPAGSGNDTARGFGIPLAAGAALDAALQDRCLEADLLSGADGLTLTAVASGFDAQVAVNVNRSRYKRLCNAIGAGRLAYLIGILHTLMTFKPCRVSVTCDGKEQAFEKAWLVSVCNLPSYGGGLLICPQAKAGDGLLDVCVVHGLSRGQLLRLLPTVVKGKHTQLPFVTMLSGRSAAVRFAEPRQAIGDGESLGTVPQAVRCEPGALRVLSPLASAQGAARPCSASG
>NZ_LN831776.1|WP_039835617.1|719182_719776_+|xanthine-phosphoribosyltransferase
MELLRHKVISEGIVLGQGVLKVDSFLNHQMDPFLMREVGREFTRRFAGEGVTKVLTIESSGIAPGIMTALELEVPLIFARKQKSLTLTEDIFVEKVYSFTKKESNEITVSKKFIAPGERVLIVDDFLANGEAAFGLARIVEQAGGTVAGIGIVIEKAFQPGNRLLKEAGYRVESLVRIASLDEGVISFVEDEAEPAD
>NZ_LN831776.1|WP_020427146.1|718832_719138_+|hypothetical-protein
MECIVHFEVDHTEGVKPLRGLLFLDEGQTPGEQELIDMFKDMKFAVRLDDREKLIFKPVNPGENYSQIRITGFDSGKPNSKEDHELKSLVGNLLPQKPTGL
>NZ_LN831776.1|WP_020427144.1|717116_717893_+|zinc-ribbon-domain-containing-protein
MNFLQRLKDGASRVSEKAQSSVEIGKLNGQISDIEREMEIEFMKMGKLFYEGYRSRDMSVAEGKMVELSRGCFKYQEQIDELRARIAELKNERLCACGHVVALDANFCPHCGRKLEELSPRKEAAAVNVHTVHKHEVEEDEFYGEDELTEAEKELAMRHEHRAVYTEVLPEEEELPLENYAGTAQAEERSRREADQLERERERQLELDRRIRDWKASEPEEAAVSEDGGVRDIVKCQICRADLPKGSMWCPRCGSEQI
>NZ_LN831776.1|WP_046501106.1|727452_728379_+|cytochrome-c-oxidase-assembly-factor-CtaG
MLGLSYFSFAELWSPLFLAVMLLLTAGYFVLIGPLSGRFQGSSQVPLWRRFSFIFGMLALYLAQGGPLSLLGHILFSFHMASMAFSYLVAVPLIMLGIPDWCWRALLKGLLRPLRRVSFLAHPVVAALLFNGLFSLYHIPVIHDYVMLHFAVHRLYYAVLFLTSALMWWNLINPLPELRSINGLGQIGFIFLNMVLLTPACGLIIFAGEPLYATYSDPQTWARAMGYCVSGSPAELLQAFGGPSFFGWLSPKVDQQVGGIAMKFIQEFIFASMLAYVFYHWYKKENGQDDAEVPAPSSELEERVLTRV
>NZ_LN831776.1|WP_020427303.1|728405_728870_+|DUF420-domain-containing-protein
MDIFTVFPTISTSFIVISAVLVAIGWRLIIKGKREAHKKTMIAAAIAAVLFFIVYMSRTVFVGNTSWGGPEDLSLLYHIFLIFHIVLATVAAVFGITTLTLGFKAKYAKHRKWGRVTSVIWFITAITGVAVYVLLYIFYPGGHTKPVWEVILGA
>NZ_LN831776.1|WP_020427304.1|728977_729760_-|MBL-fold-metallo-hydrolase
MINDPWFTVQQIDETTFAISEYGHWEKVHSFLLLGQERAALIDTGLGIGNIRTITDQLTNLPIDVLTTHVHTDHIGSHGEYERIFVHEGDLDWLVHGIKGLSLEQIRRDIGRDISQPVPEGFDPQTYRPFQGEPAGLLRDGDTVELGGRALAVYHTPGHSPGHLVFWDTLNGYLFTGDLLYDGTPVYAFYPSTSPVDLVASLERIAEIDGVQRIYGSHNTLGLHPQILSEVKHAVQLLRRNDLVKFGTGLHTFNGFSIQF
>NZ_LN831776.1|WP_020427305.1|729991_730720_+|hypothetical-protein
MTTIKDAWVIVRSDFRADKLKLLRALIFAVLFTVYMSIFSEMIIGDVLESGDGKVLADFLLISMTPMLGFTFSRRTMKYFSEDSYTRMLAYMRSLPVPAAVVLCKRKLHTVFSFTLNGVLYFGLIYAMSGQLRSELSIPAYLAFALTWVGFALVLTGLYIFIELMVSGKTYCWLLLLITLLCLGVALLVGEAGGNLFLYSIWYAKEWGLASPLMWATLLLGTVSVQLFSKWTIYRLKSRDLV
>NZ_LN831776.1|WP_020427306.1|730780_731176_+|GntR-family-transcriptional-regulator
MWIPIQINENSAEPLYHQIETQLKSLIISGVITEGTLLPSIREFAGDLKCSVITVRRVYQDLENEGLLRTRQGTGTFVSHVGEGAMEGYKKEAIRKALENAVDVGLSVQCSEAELTELFTEIVKHKYGTQT
>NZ_LN831776.1|WP_020427307.1|731192_732125_+|ABC-transporter-ATP-binding-protein
MVQQAIELRNVSKKRRQGKTIGPLNLNLPQGYITALVGQNGSGKSTMLHMLLQLTFPDEGEIRWFEHSYADGLPLALRQRIAYVPENPQAEEKYWSAAEAAEFRRHWYPAWDQDFFEALLAKFEVPEDAKLGKMSKGERRKFEIAAALAARPQLLLLDEPSSGLDPFAWKAMIETLRKYMDESGATVVISTHIVEEVRRLADYIVLMHHGQLLGMAEKDSLFGSWSEIWVQVENEEELGELAQELPGALHFAIDTPGVASFITPQAQQNEKRVQDLGVKVIKSRILELDEILSLWTQGHRPALIDQERGD
>NZ_LN831776.1|WP_039833127.1|732129_733032_+|ATP-binding-cassette-domain-containing-protein
MEALKLEQVMKQYGDKTAVNGISLKVEPGEIYGLLGANGAGKTTTMRMVLGLIYPDGGKILYNGKPFSDELQHMMGYLPEERGLYPKVKVSDQIIYLARLRGMSAGDAEKSLRFWLERFDVPEYYNKKIEELSKGNQQKMGFIAAVVHKPQILILDEAFSGLDPVNVELLKDTVKELRDQGTSILFSTHRMEHVEELCRNITILDRSNTVVQGDIREIKKGYPREEVALRTAGELSGLDKIPGVSAVQKQERGYLLSISEIGAAQRILQHAMAAGEVEHFEIKEPTLNQIFIRAVGESNE
>NZ_LN831776.1|WP_020426612.1|733024_734323_+|ABC-transporter-permease
MNKMGTIISFTFKNKVRTKSFLITTLILILLISIGMNIPYFIKVFQGDDGAKNTQIGVVAEQGNRAAELLLAYAPPAAADADEDTDTVAFTAFASADDAALKQGLDDDKIEGYLTFDAKGSEGVPPVTYHSKDGELDKDLKTYLQGALQQINTQLIAGDKLTQEQVAAMFAPVSIGTQQLSTDGKDGAATDESKPAINYVIVYVLLILFFMSITMTGNMISAEVTSEKSSRIMEILITSASPLTQMFGKVIGIFLVGLMQIAIISGSIAVNLMLPHNASILTDFDLDLGQLNYGILVYGFILYVLGYFLYALMYAAVGSIVSRTEDLGQALMPVMMCTFVAFYIPLFSISAPDTMLIKVASFVPITSPLSMVLRIGVGEVAFWEIAVSLVILLATTFGLGWLAAKIYRTGVLMYGKRPSIKEIRKAMKAYKI
>NZ_LN831776.1|WP_052741407.1|735179_735947_+|hypothetical-protein
MKAMKKLFAGLMMFTLIFGVSFVGSAFASGDEVKLIDSDISVMYKNGYVGFSGNIDVANLGPVKNVTVHYTTDDTNWYDTTATYVGPTDVNREKWHFGISRTDGSKDHLELKDPKFIKFAIKYEVNNQIYWDNNGGANYYNEVNSSYPLSSVILGAPNVLNDKSTLSNGEFSGYIFVKNLNPTKTVKVVYTTDNWATTHEVFAAYGGSVNNFNSVESWKYSINVPGATNVKYAISYTTGGQTYWDNNYGHNYEVN
>NZ_LN831776.1|WP_081487276.1|736036_736273_-|hypothetical-protein
MEKENDSNIISDREFLTLLQAAKRKDPAATLQLVNLFKEDILKVSRYIHLPVEDAVSMITLEFLELIQGENHEPMLPE

Crispr_ID: NZ_LN831776_10

• CRISPR_ID: NZ_LN831776_10
• CRISPR_location: 772493-772581
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_10

Consensus_repeat	Method
AAGTTTTGTGAGCTTAAGCATCA	CRISPRCasFinder

spacers of NZ_LN831776_10

>10.1|772516|43|NZ_LN831776|CRISPRCasFinder
CCCGAACCGCTACGTACAAAACTTGCTTCGGAAGCATAGGCTT

CRISPR arrays and Neighbor proteins around NZ_LN831776_10

CRISPR arrays

The CRISPR arrays of NZ_LN831776_10

>merge|NZ_LN831776|10|772493-772581|CRISPRCasFinder
AAGTTTTGTGAGCTTAAGCATCACCCGAACCGCTACGTACAAAACTTGCTTCGGAAGCATAGGCTTAAGTTTTGTGAGCTTAAGCAACA

>NZ_LN831776|10|10|772493-772581|CRISPRCasFinder
AAGTTTTGTGAGCTTAAGCATCA	CCCGAACCGCTACGTACAAAACTTGCTTCGGAAGCATAGGCTT
AAGTTTTGTGAGCTTAAGCAACA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020428250.1|772675_774235_-|HAMP-domain-containing-sensor-histidine-kinase	unknown	unknown	gnl|CDD|274368
NZ_LN831776.1|WP_046501117.1|768726_769659_+|UTP--glucose-1-phosphate-uridylyltransferase-GalU	unknown	unknown	gnl|CDD|224131
NZ_LN831776.1|WP_020427457.1|760877_761984_+|endospore-germination-permease	unknown	unknown	gnl|CDD|273333
NZ_LN831776.1|WP_020427458.1|762115_762742_+|alpha/beta-hydrolase	unknown	unknown	unknown
NZ_LN831776.1|WP_020427460.1|763092_763896_+|phosphotransferase	unknown	unknown	gnl|CDD|162743
NZ_LN831776.1|WP_020428251.1|771909_772476_-|FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|273540
NZ_LN831776.1|WP_046501115.1|765448_767629_+|glycosyltransferase-family-39-protein	unknown	unknown	gnl|CDD|224720
NZ_LN831776.1|WP_020428245.1|780280_780763_-|GAF-domain-containing-protein	unknown	unknown	gnl|CDD|224867
NZ_LN831776.1|WP_020427459.1|762781_763078_+|antibiotic-biosynthesis-monooxygenase	unknown	unknown	gnl|CDD|225209
NZ_LN831776.1|WP_020427463.1|767719_768706_+|glycosyltransferase-family-2-protein	unknown	unknown	gnl|CDD|133030
NZ_LN831776.1|WP_020428248.1|775387_776551_+|glucose-1-phosphate-adenylyltransferase	unknown	unknown	gnl|CDD|179997
NZ_LN831776.1|WP_020428244.1|781003_781303_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427461.1|763952_764498_+|DUF1697-domain-containing-protein	unknown	unknown	gnl|CDD|377954
NZ_LN831776.1|WP_020428246.1|777726_780159_+|glycogen/starch/alpha-glucan-phosphorylase	unknown	unknown	gnl|CDD|340853
NZ_LN831776.1|WP_020428240.1|783707_784175_-|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_LN831776.1|WP_046501121.1|769980_771435_+|transposase	unknown	unknown	gnl|CDD|372705
NZ_LN831776.1|WP_082118065.1|782048_783566_+|MFS-transporter	unknown	unknown	gnl|CDD|341045
NZ_LN831776.1|WP_020428247.1|776575_777679_+|glucose-1-phosphate-adenylyltransferase-subunit-GlgD	unknown	unknown	gnl|CDD|273966
NZ_LN831776.1|WP_020428243.1|781461_782013_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|224584
NZ_LN831776.1|WP_020428249.1|774231_774918_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020428250.1|772675_774235_-|HAMP-domain-containing-sensor-histidine-kinase	gnl|CDD|274368	TIGR02966, Phosphate_regulon_sensor_protein_PhoR, phosphate regulon sensor kinase PhoR. Members of this protein family are the regulatory histidine kinase PhoR associated with the phosphate ABC transporter in most Proteobacteria. Related proteins from Gram-positive organisms are not included in this model. The phoR gene usually is adjacent to the response regulator phoB gene (TIGR02154). [Signal transduction, Two-component systems].	7.57016e-67
NZ_LN831776.1|WP_046501117.1|768726_769659_+|UTP--glucose-1-phosphate-uridylyltransferase-GalU	gnl|CDD|224131	COG1210, GalU, UDP-glucose pyrophosphorylase [Cell envelope biogenesis, outer membrane].	1.34254e-167
NZ_LN831776.1|WP_020427457.1|760877_761984_+|endospore-germination-permease	gnl|CDD|273333	TIGR00912, Spore_germination_protein_A2, spore germination protein (amino acid permease). This model describes spore germination protein GerKB and paralogs from Bacillus subtilis, Clostridium tetani, and other known or predicted endospore-forming members of the Firmicutes (low-GC Gram positive bacteria). Members show some similarity to amino acid permeases. [Transport and binding proteins, Amino acids, peptides and amines].	2.56094e-44
NZ_LN831776.1|WP_046501121.1|769980_771435_+|transposase	gnl|CDD|372705	pfam13751, DDE_Tnp_1_6, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis.	1.42559e-13
NZ_LN831776.1|WP_020427460.1|763092_763896_+|phosphotransferase	gnl|CDD|162743	TIGR02172, Fb_sc_TIGR02172, Fibrobacter succinogenes paralogous family TIGR02172. This model describes a paralogous family of five proteins, likely to be enzymes, in the rumen bacterium Fibrobacter succinogenes S85. Members show homology to proteins described by pfam01636, a phosphotransferase enzyme family associated with resistance to aminoglycoside antibiotics.	2.4143e-26
NZ_LN831776.1|WP_020428251.1|771909_772476_-|FAD-dependent-oxidoreductase	gnl|CDD|273540	TIGR01292, Thioredoxin_reductase, thioredoxin-disulfide reductase. This model describes thioredoxin-disulfide reductase, a member of the pyridine nucleotide-disulphide oxidoreductases (pfam00070). [Energy metabolism, Electron transport].	5.64363e-20
NZ_LN831776.1|WP_046501115.1|765448_767629_+|glycosyltransferase-family-39-protein	gnl|CDD|224720	COG1807, ArnT, 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family [Cell envelope biogenesis, outer membrane].	1.53509e-38
NZ_LN831776.1|WP_020428245.1|780280_780763_-|GAF-domain-containing-protein	gnl|CDD|224867	COG1956, COG1956, GAF domain-containing protein [Signal transduction mechanisms].	9.9556e-84
NZ_LN831776.1|WP_020427459.1|762781_763078_+|antibiotic-biosynthesis-monooxygenase	gnl|CDD|225209	COG2329, COG2329, Uncharacterized enzyme involved in biosynthesis of extracellular polysaccharides [General function prediction only].	9.96974e-21
NZ_LN831776.1|WP_020427463.1|767719_768706_+|glycosyltransferase-family-2-protein	gnl|CDD|133030	cd04187, DPM1_like_bac, Bacterial DPM1_like enzymes are related to eukaryotic DPM1. A family of bacterial enzymes related to eukaryotic DPM1; Although the mechanism of eukaryotic enzyme is well studied, the mechanism of the bacterial enzymes is not well understood. The eukaryotic DPM1 is the catalytic subunit of eukaryotic Dolichol-phosphate mannose (DPM) synthase. DPM synthase is required for synthesis of the glycosylphosphatidylinositol (GPI) anchor, N-glycan precursor, protein O-mannose, and C-mannose. The enzyme has three subunits, DPM1, DPM2 and DPM3. DPM is synthesized from dolichol phosphate and GDP-Man on the cytosolic surface of the ER membrane by DPM synthase and then is flipped onto the luminal side and used as a donor substrate. This protein family belongs to Glycosyltransferase 2 superfamily.	4.47119e-92
NZ_LN831776.1|WP_020428248.1|775387_776551_+|glucose-1-phosphate-adenylyltransferase	gnl|CDD|179997	PRK05293, glgC, glucose-1-phosphate adenylyltransferase; Provisional.	0
NZ_LN831776.1|WP_020427461.1|763952_764498_+|DUF1697-domain-containing-protein	gnl|CDD|377954	pfam08002, DUF1697, Protein of unknown function (DUF1697). This family contains many hypothetical bacterial proteins.	7.16224e-61
NZ_LN831776.1|WP_020428246.1|777726_780159_+|glycogen/starch/alpha-glucan-phosphorylase	gnl|CDD|340853	cd04300, GT35_Glycogen_Phosphorylase, glycogen phosphorylase and similar proteins. This is a family of oligosaccharide phosphorylases. It includes yeast and mammalian glycogen phosphorylases, plant starch/glucan phosphorylase, as well as the maltodextrin phosphorylases of bacteria. The members of this family catalyze the breakdown of oligosaccharides into glucose-1-phosphate units. They are important allosteric enzymes in carbohydrate metabolism. The allosteric control mechanisms of yeast and mammalian members of this family are different from that of bacterial members. The members of this family belong to the GT-B structural superfamily of glycoslytransferases, which have characteristic N- and C-terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility.	0
NZ_LN831776.1|WP_020428240.1|783707_784175_-|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	7.96754e-24
NZ_LN831776.1|WP_020428249.1|774231_774918_-|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	7.0001e-78
NZ_LN831776.1|WP_020428247.1|776575_777679_+|glucose-1-phosphate-adenylyltransferase-subunit-GlgD	gnl|CDD|273966	TIGR02092, Glycogen_biosynthesis_protein_GlgD, glucose-1-phosphate adenylyltransferase, GlgD subunit. This family is GlgD, an apparent regulatory protein that appears in an alpha2/beta2 heterotetramer with GlgC (glucose-1-phosphate adenylyltransferase, TIGR02091) in a subset of bacteria that use GlgC for glycogen biosynthesis. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	7.27357e-128
NZ_LN831776.1|WP_082118065.1|782048_783566_+|MFS-transporter	gnl|CDD|341045	cd17502, MFS_Azr1_MDR_like, Saccharomyces cerevisiae Azole resistance protein 1 (Azr1p), and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This subfamily is composed of multidrug resistance (MDR) transporters including various Saccharomyces cerevisiae proteins such as azole resistance protein 1 (Azr1p), vacuolar basic amino acid transporter 1 (Vba1p), vacuolar basic amino acid transporter 5 (Vba5p), and Sge1p (also known as Nor1p, 10-N-nonyl acridine orange resistance protein, and crystal violet resistance protein). MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. This subfamily belongs to the Methylenomycin A resistance protein (also called MMR peptide) and similar multidrug resistance (MDR) transporters (MMR-like MDR transporter) family of the Major Facilitator Superfamily (MFS) of transporters. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	5.82228e-72
NZ_LN831776.1|WP_020428243.1|781461_782013_+|GNAT-family-N-acetyltransferase	gnl|CDD|224584	COG1670, RimL, Acetyltransferases, including N-acetylases of ribosomal proteins [Translation, ribosomal structure and biogenesis].	1.86328e-36

Protein sequences

>NZ_LN831776.1|WP_020428251.1|771909_772476_-|FAD-dependent-oxidoreductase
MYEIAIIGAGPAGASAALFAAKAGKKTLLIDNDKGMTRRGWYENYYGIAEIGGPELVETGHKQAVKFGAELVADQAVNLTAKGEGFVIESESGAAYEAKHVILATGVMTDLAAKAGVETKDGTEPRIKTVVAVNAEGRTNIAGIWAAGTVAGVSVHAIITAGDGAKVAINIISELNGARYVDHDLLKA
>NZ_LN831776.1|WP_046501121.1|769980_771435_+|transposase
MYSIRQEELFSFEDLLLMRPEDKYSQIFEHLNLAPVLHALGKKNNRGRPEELNVPAMIYSLLIAKMEGIEFVSALVRRLRFSEEFRVQCRFTGSNRIPSEASYSRLIHVLEQTGMLEDLQDTLVLSALEEEFVTGMHLALDSSIVEAWDSLFSEAASKRRAARRAKKPSDAPVAQQLQLELTEPESEPVDERPKKPVYPPGRPSAEEKERRRKEREAYEESLGPFEKTIEQMLPYTYDELLAALPRHAARCDKKNAKGRLTSYYGFKANLLVDADCQYILSGLWSSANLNDQRMAVILLKGLLLKFPRLNVKHVLGDKGYDSAAIYQLIHSLGAYPTIPMIHHKEPPKGMNSDYNPVCSQGHTYRYDSFDAKYETLKYTQPSQCKDCPLSGSGCQKVFKIRIQTDLRKHTYPARGSESFTELYKKRTAVERVFAYLKEYFGMKRTRHRGVRARVDFQLSTLAYNLSKFALDKLNQRLRNSQQVA
>NZ_LN831776.1|WP_046501117.1|768726_769659_+|UTP--glucose-1-phosphate-uridylyltransferase-GalU
MKIRKAVIPAAGLGTRFLPATKAQPKEMLPIVDKPAIQYIVEEAVRSGIESIIIVTGRNKKSIEDHFDKSVELEQTLLEKEKLDLLREVQAISGLAGIHYIRQKEPLGLGHAISCAEQFIGGEPFAVLLGDDIMVSEPPALLQMMKLYEQSEQTIVGVQPVPRAEVSKYGIIASGGAVRGVHVVSGLVEKPSPQAAPSTNAIMGRYILKPSIFSVLSKLERGAGGEYQLTDALHEVCRNEGLLALDLQGKRYDIGDKFGYIQATLEMGLEREELRPQLVPYLRGLLGSLEDGTESLCVPQTQSGLSLLNQ
>NZ_LN831776.1|WP_020427463.1|767719_768706_+|glycosyltransferase-family-2-protein
MSTHVRYSVIIPMYNEEAVIQETYRRIKKVMGTTGEAYELLFVNDGSTDNCAQMIEEYTYWDESVKLIDLSRNFGHQIAITAGMDYSLGDAVVIIDADLQDPPELILDMIREWKNGYEVVYAKRIKRNGESLFKKWTASLFYRVLRYSTDISIPVDTGDFRLIDRKVCEELKRLPEKNRFVRGLVSWVGFRQKAIEYERDERLAGETKYPLKRMIKLSLDGITSFSYKPLKLAGYLGGLLSGAGFLYLMYVLYLALFTDAAVKGWASMIGITLTFNGFVLIILGILGEYVGRIYDETKGRPLYIVQEFYSGRKQQSAAEQRVAQLNKS
>NZ_LN831776.1|WP_046501115.1|765448_767629_+|glycosyltransferase-family-39-protein
MKWVKKLGSDVILLGVLLLAAFLYGYGIWNDQYANTYYTTAVGSMLQSFHNFFFASLDSAGSVTVDKPPVTFWIQTLSALIFGLHGWSVILPQVIGGMGSVLLVYLLVKPTFGRAAARLAALAMATTPVAAAVSRTNNIDAMLVFTLLLAAWFLFKGTKRNTTGSLLAAFALIGVGFNEKMLQAYMVLPAFYLFYLLAAKVNWKKKTGVLAACTAVLLVVSLSWAVIVDSIPASKRPYMGSSGTNSVLNLAFGYNGVARLTGDRSTGGSGGGGFPGGGGGGMIGGGEMPFWNGGEMPAMNGTGGQDGRGGTGTMNGTDGQAQGQLPGGAGGEQADGGPDGRGQASGGGGMQGQMPGGRADGEGGQGGDRQFNFGQGGRGGMNGGGMFNTGTAGPLRLFQSALSGQASWLLPFLLFGCIGIFASLRRRNFTQEHKEAIFWLAWLVPVMGFFSIAGFFHQYYLIMMAPPIAALAGSGWLRLWTYYKERAVWLSWLLPVATLATAVFQWYIIHPYDSTVGSGWSIGVLAGGIAVTVLLLALRIFKGQRQRFVHASAVLGLLVLLVGPLYWALTPITYGSNSMTPAAGPDSRSGFGGMGGGGRNGTTGVNEKLLAYLKEHNTGEKYLFAAMDYGTAGPYIIDNNEPVVILNGFNNSDVPYTTETLKALVASGKVKYFLVTTGGMGGGGGRGGNSEITNWITENGTAVPAEEWQGTVTGGNEGTLYEVTVQ
>NZ_LN831776.1|WP_020427461.1|763952_764498_+|DUF1697-domain-containing-protein
MNTYIALLRGINVGGNKIIKMQALKAMFESLGYSRVRTYIQSGNVVFESNEAQAAELEAVISAAIKETFGFDVSVMIRTLEELEAAIAGNPFEPPAEEGYKRLYISFLAEAPSKEALEKLRPYEEGADKLHVAGKEMYTLYEVSASQSPLFKVQLDKLLGTSITARNWNTVNKLAAMGREQ
>NZ_LN831776.1|WP_020427460.1|763092_763896_+|phosphotransferase
MTGKRIGEGRTAEVQEYGTGKILKLYRADIPAEYVEHEYEVSKYVHKQGIQTPQPIELVTLGERKGILFQQIHGSSMLRLIGEKPWRLGEYARQLASLHHDLHKLQGPEAFGKQKESLRSSIVAAPMLTMEEKTPVLEKLEQLPEGDRLLHGDFHPDNVLIDGQAWTIDWMTGMSGNPAGDAARSVMMFSMGALPPGASLSTRLVTGFIRQRLTKGYIREYLRLSGLSYAEVNAWVLPVASARLTEGIPLAEKEQLVREIRRRLRSK
>NZ_LN831776.1|WP_020427459.1|762781_763078_+|antibiotic-biosynthesis-monooxygenase
MILEAAMLQIRPGLTSQFEQSFKAASVLISSIEGYLGHELQHCLEDDHKYLLLVKWRNLEDHTIGFRESSQYQEWKAMLHHYYSPFPVVEHFTRINLA
>NZ_LN831776.1|WP_020427458.1|762115_762742_+|alpha/beta-hydrolase
MSVSSIVMSSHWGREVRHKYITQESKALAVVFPGKNYSAERSLLDYAAKLAREYGCDILLLEYGYQSARTELKRDEIDIIAEECKAAISSLPEYEQLLFISKSMGAVIAGRVAAELNLSQKTSHLYLTPVADSLPLLRQSRGSIIYGGSDPTFTEQHAAGLNGQKNLRVYRIDDANNALEVGSVNESLAVLLVIINFYHEFFRDALTG
>NZ_LN831776.1|WP_020427457.1|760877_761984_+|endospore-germination-permease
MSKEIIPAGQAISISVLFIIGTSLFMGSSGQSGNSSWIALILAAALAVPLMLIYARLHGLFPGKDLYDMLILVFGAVAGRMLSCLYIWYALHLGSMVLRNFGEFSKTVALTSTPMLAPMLVIGLLCVWVVKAGMEVLGRSAKFLLLFTIMVIAVIELLSIPKYQYHHLLPVLDSGWKLVLSDTIGSFTFPFAEIVVFLGAFNVLPKKGSAAKVLVSSTMIAGVIILVVTLRNLMVLGPDILSSLYFPSYVAVGRINIGDFLTRIEGSSAIIFVTALFIKVSLCLYAASNGMAKVFKLDSYRSVVLQLGLIMVYLAVFIYKDIMQMQYFAYHIYKIYALPFQVAIPVILWVTAEILAWRRSGKKTAAQQ
>NZ_LN831776.1|WP_020428250.1|772675_774235_-|HAMP-domain-containing-sensor-histidine-kinase
MIARITGFFGSLPAPHSLRKQLLVISLLILSGLLLLIGVLQYVLMRDFIYSNRAESMETQIRSVPREIFSSPPAWGAGGIDASGMSSGEAGSPDTGSPGNRPPGNLRNTGRRPLLLDAHTTIAVYSADGGFKDFQEETLSDSPAPRLTDAEYNDLLKHTTDKANGGYRLMAAPDGSEHLAVFMNLGKPQEARMLLQMSVSTGPLKDVIMQQLLIFAALSVVALLAGLLLYLPALRKTLVPLSNMGEAAEIIDAGNLSERFPVHQGQTEIDKLSRSFNGMLERLEISFHNEREAKEQMRRFAADASHELRTPLTSIHGFLEVLLRGAADNREQLMGALTSMHGESKRINKLVEDLLLLARMDGAPQLNIKGMMLGEIIAEMQPQLLMLAGDRRVTFDISPGIRGMYDPDKLKQVILNLFQNAVQHTDAHKGTIHISLTARGTEAELAVQDNGSGIAAEHIPHVFERFYRSDSSRTRKYGGSGLGLSITKSIVDAHHGGIRVESRPGEGTTFRVTLPRSVE
>NZ_LN831776.1|WP_020428249.1|774231_774918_-|response-regulator-transcription-factor
MKAAQGVKLLLVDDEPHILQFLELGLINEGFEVRTAPDGASAIAVAADFKPHVAILDVMMPGMDGFELCRYLRSEESELAVIMLTAKDEVDDRVKGLSIGADDYMVKPFSFDELLARIQARLRNQFPGLLGEVRCGPFRIDGRRKEIRHKDEVLELSPTEYELLQYLVINHGLVLSKPMILDKVWGYDFGGEENIVEVYIRSLREKLGDKDHRIIRTLRGAGYRVDLV
>NZ_LN831776.1|WP_020428248.1|775387_776551_+|glucose-1-phosphate-adenylyltransferase
MKKKEMVAMLLAGGQGKRLKGLTKSLAKPAVYFGGTYRIIDFPLSNCSNSGIDTVGVLTQYEPLVLHSYIGVGSDWDLNRKDGGVFVLPPHERENGSSWYRGTADAIYRNLKFVDQFDPEHVLILSGDHIYKMDYHAMLQYHKARNADCTISVIDVPLEEASRFGILNTEEDLKIYEFDEKPAKPKSTLASMGVYIFKWEVLRKHLLEDGENSGSSHDFGKDIIPLMLADGQSLYAYPFEGYWRDVGTVASLWEANMDLLSDTPPLNLNDPDWRIFTRNPNQPAQYVAPGAKVSGCIINEGCIVHGEVKHSVLFYGVEVGEGSVITDSVIMPKVKIGKNVKIHKAIISENTVIEDYMEIGIERENEDEILLIDNRSKKRQSVAAKTI
>NZ_LN831776.1|WP_020428247.1|776575_777679_+|glucose-1-phosphate-adenylyltransferase-subunit-GlgD
MKELMGVINLDHELDQLNELTYFRCGAAVPFASRYRLIDFVLSNMMRAELESVGLFVRRKYRSLMDHLGDGKSWDMNRKHGGLFILPPDWNDPTDTSLGDLQHYHNNLDFFKRASAKYIVFSGSQHINTADLQEVYQYHLEKGADVTLVYKKIEELQPEHDPCLRVEVDEDSNVTEIHQEKDHPNVYLDIFIMEKKLFLEQVEYCIAHGESYFFRDAIQKNRHKFKIAAYEYTGYHAVINSLESYYKNSLNLLQQDNYFGLFKENPVQTKIKYEAPTRYLDSAEVSNSLVANGCIIAGTVENSVIFRGVQIRKGARIVNSVIMQKCVIEENAVIENVIMDKDVHLSRERILVGDSKRPFVIAKSSKI
>NZ_LN831776.1|WP_020428246.1|777726_780159_+|glycogen/starch/alpha-glucan-phosphorylase
MFNDKETFKEVFRKTLIGKLGKPLEEASNADIYNILGNMIREDVGKNWAETNQKFKADKDKQVYYFSMEFLIGRLLGNNLLNMGVLEVVRDGLAELGFSLRDVEEEEADAGLGNGGLGRLAACFLDSLASLQYAGHGCGIRYKYGLFEQKIVDGYQVELPDYWLQNDNVWEVRREDKQVEVRFWGHVETDEVNGELVFEHKDYEAVRAVPYDVPIIGADRRHVNTLRNWSAESITQPSRMFGSLAGSDYHKFLEYKRSVESISEFLYPDDSQYEGKLLRLKQQYFLCSAGVQSILRTFSKTGLGIESLPDKVALHINDTHPTLVIPELMRILMDVNGLGWDQAWSMTTRMVSYTNHTILSEALEKWPIGMVRELLPRIFLIIEEINARFCGELMSKYPGDQNRINQMAIIHDDQVRMAHLAIVASHSVNGVAALHTEILQKREMRLFNEMYPHRFNNKTNGITHRRWLLHANPELAGLINESIGTRWVHHPQEMIGLIKYSEDASFQQQVAGIKRRNKQRLGEYIFSKHGIQVDPDSIFDVQVKRLHAYKRQLLNVLHIMHLYNQLKDNPSMDMVPRTFIFGAKAAPSYHLAKRIIKLINTVADVVNKDPEIKGKIRIFFLENYSVSLAEKIIPAADVSEQISTASKEASGTGNMKFMMNGALTIGTMDGANVEMHEMVGDNNMFLFGLRAEQVMDYYQYGGYHARDIYNGDGRVKEVLDQLVTPGPICCNTQEFDTLYQSLIDNNDEFFVLKDFASYVETHVNIDLAYRNQKEWLKKSIINIGHSGKFSSDNTIARYASEIWNINPVQL
>NZ_LN831776.1|WP_020428245.1|780280_780763_-|GAF-domain-containing-protein
MFQAMPYDGTRSERYESVLSQLGALMEGEPNAIANLANASALLKFSLPDTNWAGFYLFDGKELVLGPFQGLPACIRIPLGKGVCGTAASERRTLVVGDVHAFPGHIACDEASNSEIVVPLVQGDRLLGVLDIDSPIKHRFDDEERRFLERFAGMVAEVIR
>NZ_LN831776.1|WP_020428244.1|781003_781303_+|hypothetical-protein
MRADVQNLFIGIHMLYHAHEKDLTLTEMLPELENLGYRVAEREVKQELERLSQENFLTAHGEAYSLTGTGIEEFKAIQDKLKVLCTEVLKPVKAAGASG
>NZ_LN831776.1|WP_020428243.1|781461_782013_+|GNAT-family-N-acetyltransferase
MYVSGGVIPDLPGKKVKLRPLEAGHAAALYSVWSHPQVNRWLAAPLLSSPEEAEQLIAVLLQMSREEESLRWSIIGPEGGVIGSCGYNSWQLQGAYRGEIGCELLPDYWGLGYMREALELLLDYGFAVMGLNRIEAFCHPDNLRAQRLFQSLGFQREGLLREYRHTDAGFQDVVLYALLRGSR
>NZ_LN831776.1|WP_082118065.1|782048_783566_+|MFS-transporter
MDSLISPGTKERKLILTGVLLATFLAAIEGTVTGPAGPAIVGDFQGMQWLSWIFTAYLLAMAVTTPIFGKLSDLMGRKPVFIGGVAVFLLGSLLCGVAQSMEQLIVFRGLQGIGAGALIPMTFTIIGDIYSIQERAKTQGLLSSVWGISSLVGPLLGGYVVDYLSWRWVFVFNLPFGLLSIVFISRFLKEENVRRKAKLDLPGVLLFAAGMGALLFGLTTGGQNLPWTSPLLLFLLAASVAVLVIFWRVERRASEPMLPLGLFSIRNITVSTGANLLVSTLIIGLTTYVPLWVQGVSGGSAALSGLLLAPMSVGWVLGSFAGGRMILRSGSRQTGVLGLSLIVLGAGGLIFMTAESPQLLLLGLMLACGVGFGYASIVFTIIAQSSVEHSQRGASTALNTFTRSLGQTVGVAIFGSWLNLNVKWQLDGAPGSAEAGTDINQLLHPQGESALSSEAWGSLKSALEGGLHSLFIVMAVFAVLSLLITMGLRKGLPSLKEEPAAQKEA
>NZ_LN831776.1|WP_020428240.1|783707_784175_-|MarR-family-transcriptional-regulator
MIQSYERDTQLTLHLYRVFAKSFKSINEHAVTGSKIEGFNPTAFAVMEVLYYKGPQPIQQIGAKLLLQSGNVTYVIDKLEERGYLQRKPCPSDRRVIFAELTSEGERLMNEMYPKYSERLHLAFSGLSDEEKEQMITLLKKMGLQAEKLSPLPRK

Crispr_ID: NZ_LN831776_11

• CRISPR_ID: NZ_LN831776_11
• CRISPR_location: 796021-796162
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_11

Consensus_repeat	Method
CTTGTTCAGTGCCGCTGGCACCTCAAACGGGCAGCCTGCTGTGGACGGCGGC	CRISPRCasFinder

spacers of NZ_LN831776_11

>11.1|796073|38|NZ_LN831776|CRISPRCasFinder
TCTATAGAGCCGTTTGCGGACGGCAACGGCAATCCCAG

CRISPR arrays and Neighbor proteins around NZ_LN831776_11

CRISPR arrays

The CRISPR arrays of NZ_LN831776_11

>merge|NZ_LN831776|11|796021-796162|CRISPRCasFinder
CTTGTTCAGTGCCGCTGGCACCTCAAACGGGCAGCCTGCTGTGGACGGCGGCTCTATAGAGCCGTTTGCGGACGGCAACGGCAATCCCAGCTTGTTCAGTGCCGCTGGCACCTCAAACGGGCAGCCTGCTGTGGACGGCGGC

>NZ_LN831776|11|11|796021-796162|CRISPRCasFinder
CTTGTTCAGTGCCGCTGGCACCTCAAACGGGCAGCCTGCTGTGGACGGCGGC	TCTATAGAGCCGTTTGCGGACGGCAACGGCAATCCCAG
CTTGTTCAGTGCCGCTGGCACCTCAAACGGGCAGCCTGCTGTGGACGGCGGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020428237.1|786694_787945_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|377581
NZ_LN831776.1|WP_020428238.1|785924_786698_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|224054
NZ_LN831776.1|WP_020428239.1|784507_785806_+|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_LN831776.1|WP_020430616.1|801658_802837_-|DUF2935-domain-containing-protein	unknown	unknown	gnl|CDD|223678
NZ_LN831776.1|WP_020430611.1|798035_798455_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831776.1|WP_039790050.1|805198_806077_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_020428232.1|792943_793762_-|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|225176
NZ_LN831776.1|WP_020430614.1|800653_800905_+|YneF-family-protein	unknown	unknown	gnl|CDD|367606
NZ_LN831776.1|WP_020428236.1|788180_789452_-|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|367519
NZ_LN831776.1|WP_020428231.1|794286_794685_+|holo-ACP-synthase	unknown	unknown	gnl|CDD|234610
NZ_LN831776.1|WP_020428233.1|792062_792872_+|ammonia-dependent-NAD(+)-synthetase	unknown	unknown	gnl|CDD|234831
NZ_LN831776.1|WP_020430613.1|799332_800550_+|tRNA-epoxyqueuosine(34)-reductase-QueG	unknown	unknown	gnl|CDD|272993
NZ_LN831776.1|WP_020428240.1|783707_784175_-|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_LN831776.1|WP_020430610.1|796838_797447_-|superoxide-dismutase	unknown	unknown	gnl|CDD|223678
NZ_LN831776.1|WP_020430612.1|798696_799314_+|signal-peptidase-I	unknown	unknown	gnl|CDD|274044
NZ_LN831776.1|WP_020430617.1|802918_805165_-|hypothetical-protein	unknown	unknown	gnl|CDD|283786
NZ_LN831776.1|WP_020428234.1|791506_791941_+|BrxA/BrxB-family-bacilliredoxin	unknown	unknown	gnl|CDD|377667
NZ_LN831776.1|WP_020430620.1|806094_806985_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_LN831776.1|WP_020430615.1|800955_801549_+|GTP-cyclohydrolase-I-FolE	unknown	unknown	gnl|CDD|236472
NZ_LN831776.1|WP_167345578.1|789698_791378_+|PAS-domain-containing-sensor-histidine-kinase	unknown	unknown	gnl|CDD|236901

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020428237.1|786694_787945_+|ABC-transporter-permease	gnl|CDD|377581	pfam05975, EcsB, Bacterial ABC transporter protein EcsB. This family consists of several bacterial ABC transporter proteins which are homologous to the EcsB protein of Bacillus subtilis. EcsB is thought to encode a hydrophobic protein with six membrane-spanning helices in a pattern found in other hydrophobic components of ABC transporters.	1.01663e-55
NZ_LN831776.1|WP_020428238.1|785924_786698_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	2.24152e-71
NZ_LN831776.1|WP_020428239.1|784507_785806_+|MFS-transporter	gnl|CDD|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	9.07094e-60
NZ_LN831776.1|WP_020430616.1|801658_802837_-|DUF2935-domain-containing-protein	gnl|CDD|223678	COG0605, SodA, Superoxide dismutase [Inorganic ion transport and metabolism].	4.02427e-98
NZ_LN831776.1|WP_020430611.1|798035_798455_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	2.43815e-19
NZ_LN831776.1|WP_039790050.1|805198_806077_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	5.2004e-57
NZ_LN831776.1|WP_020428232.1|792943_793762_-|alpha/beta-hydrolase	gnl|CDD|225176	COG2267, PldB, Lysophospholipase [Lipid metabolism].	9.143e-07
NZ_LN831776.1|WP_020430614.1|800653_800905_+|YneF-family-protein	gnl|CDD|367606	pfam03672, UPF0154, Uncharacterized protein family (UPF0154). This family contains a set of short bacterial proteins of unknown function.	9.03456e-11
NZ_LN831776.1|WP_020428236.1|788180_789452_-|NAD(P)/FAD-dependent-oxidoreductase	gnl|CDD|367519	pfam03486, HI0933_like, HI0933-like protein.	0
NZ_LN831776.1|WP_020428231.1|794286_794685_+|holo-ACP-synthase	gnl|CDD|234610	PRK00070, acpS, 4'-phosphopantetheinyl transferase; Provisional.	1.43168e-44
NZ_LN831776.1|WP_020428233.1|792062_792872_+|ammonia-dependent-NAD(+)-synthetase	gnl|CDD|234831	PRK00768, nadE, ammonia-dependent NAD(+) synthetase.	1.52727e-114
NZ_LN831776.1|WP_020430613.1|799332_800550_+|tRNA-epoxyqueuosine(34)-reductase-QueG	gnl|CDD|272993	TIGR00276, iron-sulfur_cluster-binding_protein, epoxyqueuosine reductase. This model was rebuilt to exclude archaeal homologs, now that there is new information that bacterial members are epoxyqueuosine reductase, QueG, involved in queuosine biosynthesis for tRNA maturation. [Protein synthesis, tRNA and rRNA base modification].	7.98332e-173
NZ_LN831776.1|WP_020428240.1|783707_784175_-|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	7.96754e-24
NZ_LN831776.1|WP_020430610.1|796838_797447_-|superoxide-dismutase	gnl|CDD|223678	COG0605, SodA, Superoxide dismutase [Inorganic ion transport and metabolism].	4.49134e-111
NZ_LN831776.1|WP_020430612.1|798696_799314_+|signal-peptidase-I	gnl|CDD|274044	TIGR02227, Inactive_signal_peptidase_IA., signal peptidase I, bacterial type. This model represents signal peptidase I from most bacteria. Eukaryotic sequences are likely organellar. Several bacteria have multiple paralogs, but these represent isozymes of signal peptidase I. Virtually all known bacteria may be presumed to A related model finds a simlar protein in many archaea and a few bacteria, as well as a microsomal (endoplasmic reticulum) protein in eukaryotes. [Protein fate, Protein and peptide secretion and trafficking].	3.08885e-49
NZ_LN831776.1|WP_020430617.1|802918_805165_-|hypothetical-protein	gnl|CDD|283786	pfam06202, GDE_C, Amylo-alpha-1,6-glucosidase. This family includes human glycogen branching enzyme AGL. This enzyme contains a number of distinct catalytic activities. It has been shown for the yeast homolog GDB1 that mutations in this region disrupt the enzymes Amylo-alpha-1,6-glucosidase (EC:3.2.1.33).	7.09693e-83
NZ_LN831776.1|WP_020428234.1|791506_791941_+|BrxA/BrxB-family-bacilliredoxin	gnl|CDD|377667	pfam06491, Disulph_isomer, Disulphide isomerase. This family of proteins has disulphide isomerase activity, EC:5.3.4.1. It has a similar fold to thioredoxin, with an alpha-beta-alpha-beta-alpha-beta-beta-alpha topology. It has a conserved CGC motif in the loop immediately downstream of the first beta strand. This motif is essential for activity.	4.85624e-89
NZ_LN831776.1|WP_020430620.1|806094_806985_-|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	4.79663e-113
NZ_LN831776.1|WP_020430615.1|800955_801549_+|GTP-cyclohydrolase-I-FolE	gnl|CDD|236472	PRK09347, folE, GTP cyclohydrolase I; Provisional.	3.29825e-108
NZ_LN831776.1|WP_167345578.1|789698_791378_+|PAS-domain-containing-sensor-histidine-kinase	gnl|CDD|236901	PRK11360, PRK11360, two-component system sensor histidine kinase AtoS.	2.63819e-56

Protein sequences

>NZ_LN831776.1|WP_020428231.1|794286_794685_+|holo-ACP-synthase
MIYGIGHDVLEIGRVAGIANGSLGSRFTRRILTAQELVLAAGKGGKAAEFIAGRFSAKEAVVKALGCGIGHTVGFQDIEILPDALGKPVASLSAEAWSRLRLPEQEYTIHLTITHSRGLASAFAVVERLRGY
>NZ_LN831776.1|WP_020428232.1|792943_793762_-|alpha/beta-hydrolase
MPRNFELPAGEDAVLRCSHFPAQGEAKSLVVVAHGYKGFKDWGMFPYVAEALSDEHEVISFNFSHAGIGEDLQNFTELEKFARNTYQREIKDMEILLSYLSQHHRFGSLPVFLLGHSRGGGDCLLYALDHPAELAGVISWNGTTNLDLFTEEQKREMRETGRTHVLNGRTGQQMPLDAIIIEDLEQQAERYNILERMKQAAFPAVLIQGSEDGERLRRGSEQLIRFRPDIEWIQIPGGNHTFGTVHPFTGTTPQLEQAISASRDFITRVLEE
>NZ_LN831776.1|WP_020428233.1|792062_792872_+|ammonia-dependent-NAD(+)-synthetase
MSMQSEIIAALGVKPSIDVEAEVRKRVDFLKAYVLEAGAGGLLIAISGGVDSAVAAGLCKRATDELTAEEGKDYMTLGVFQPYGEQEDIEHSYAVAEAFGLTHRAETNIEEAVNEIALEVEHSLKSLGQHRHITHQGKGNVKARTRMVMQYALAFENNLLVVGTDHASEAITGFYTKWGDGAVDITPLSSLNKRQVRQLAAFLGVPADIVTKAPTAGLWPGQTDEAELGITYEENSDYLEGKTVSPEAAKKLENFYRRTAHKRNVIPGI
>NZ_LN831776.1|WP_020428234.1|791506_791941_+|BrxA/BrxB-family-bacilliredoxin
MSMSFNQYMKDSIQPMRDDLTSIGFKELLTPEEVEAVLPDSKGTTLVVVNSVCGCAAGQCRPGVAQALQNEILPDHLYTVFAGQEKEATAKAREYFAPYPPSSPSIALMKDGQLVHFIERHGVEDRSAAEIAAELKDVFNRLCQ
>NZ_LN831776.1|WP_167345578.1|789698_791378_+|PAS-domain-containing-sensor-histidine-kinase
MFKWWIDQGHIVRRNGKFPDDQSFLILSCALSIVFCMFLSTTLFGAIYLNLAMIPAYIGILYAGFRSGISLAVFFILCTALFSEPPGLSNLVLNTGVLLYPLLFGMAKPFKSENIMGKIFILWSVLFPSMMFIVLAPKMYGPSLYDTSPKEMAVALFYLLVPVILGGSLLYFIETAWDRQQTQEKMKGISEKFERESEKLQQITNVVPVSIMLLDDMGYVTEINDCMLDLFRQHEPGITREAIVGQQAERLLLQEINGEALKRMKDSGFSKQRYNEKVQYDSRTYNVFSAPLQQGLGGGSGGRVLIVQDLTEEEKFRSELDNVERLTLVGQMAAGITHEIRNPMAVVRGFLQLMREKSPGEMDSYYQIVIEELDRANGIINDFLSLAQSRISDKEPVQLHHIIKELAPLLWADANLRGQSVELRLCPSLPLLQLNPREIKQLILNLARNGMEAMEPKGELLLETHFNENKVELIIQDTGSGIPQSQLEKLFVPFYTTKNQGTGLGLPLCLSIAERHHGSIRVESQVGKGTAFIVSFPYVQEGRQQAAATKEHSDSPPQP
>NZ_LN831776.1|WP_020428236.1|788180_789452_-|NAD(P)/FAD-dependent-oxidoreductase
MSGNYDVIIIGGGPSGLMASVAAAEHGAAVLLVDKGSRLGRKLGISGGGRCNVTNAKETAELISHIPGNGRFLYSAFDHFNNLDIIRFFENLGIALKEEDNGRMFPVSDKASSVVSALIGKVRSLGVQMITDSPVAEVLYGNGSVKGVRLTTGRTLSASAVVIATGGKSVPQTGSTGDGYPWAEAAGHTITELFPTEVPILSREGWIKSGELQGLSLRDVTLTVWNPKGKRVIAHRGDMIFTHFGLSGPIALRCSQFLRQVQRKSGTDTVELSIDLFPDLNPQEMEEQLQNKLELEPKKALRNSLKGLLLERMIPLLLAKAELDGDTTGHHLPKSGLQALAALLKRLPVQVYGTRSLEEAFVTGGGVNLKEINPRTMESKLMPGLFFCGEILDIHGYTGGYNITAAFSTGYTAGKHAAEQYRK
>NZ_LN831776.1|WP_020428237.1|786694_787945_+|ABC-transporter-permease
MSREAFAFPTAPKLFKRRLFSHFREQSAIIRTAADWTVLLYIIIPGGLLGGRFYYGFWNHELPAWTAALPFALILALLAILIANGGLVLLLQEGDLLFLRQRENWIRTIVLRGTIYSLAVTSLKMAAVYAILLPFIVRGYGVSPAAAWALLVLTLACSWCVKLLGHIVKVQRQGFRRWLWLIPAVTVPCGIYIRAGLFWKDSPSLLLLVAAVLAAVTVWAIRYRLRLSGTFMNDVREDYKQRMRIAALLLRGVLDKPRPTRYKPWIFRKSQPLLKSKTPESRFTAAAIKALVRNPAHLKLYLSFTGVGLIAVFIVPSLLKWLIFALLVALMAYWLSSFWLLFSGDDYIGILPFTKEQKAVAGSKTLPLLLLPFSLLCSAVICTQLYGWLGLVLFIPVGGIAGYLIANMFSAFRFAR
>NZ_LN831776.1|WP_020428238.1|785924_786698_+|ATP-binding-cassette-domain-containing-protein
MEETEAPQGPELEATGDSEQESAERDTVLDVYIEEAGYEAGDRRISNISFQVQQGQLLGLIGPNGAGKSTTIKTLLGLLKHAKARVKLGGANKSYAYVPEQPVFYEDLTLWEHLDLAAAAYGLSYETFGATAEKLLSQFGMEQVRNDLPAGFSKGMKQKMMLMLGFLVQPDIYIVDEPFIGLDPRATKDFLRLLEAERRRGAGVLMSTHVLDTAEKICDSFVLISGGRMTATGTLEDIRAQAGLPEASLFDCFDELT
>NZ_LN831776.1|WP_020428239.1|784507_785806_+|MFS-transporter
MKENQENVTTAVKLTSNKPFVLLITAQLVSNIGDWLHILALLTMVGLKWQASPWEITAVSLCMAVPMLLGGPFAGYLSDKVDRKGIMIGSDLVRAGIVACLVFAGSLWQVYVLLLAKGVMDVLFSPAKSGKLKELVPPGQMDQAVALSSSIEQITKIIGPALGGLLVAAVGISACYFIDSVSYIASAVILLGLPRVGMFKTGRPNEDGDTARPSFRKEAGAGLRLIGSMPVVLSGVVMIVAALLVLQIADSQTVTLFREIPGVNADLLGWCVAASGFGTLLSALAVGRLGSGKHPLVFMGTGTLLMGSVFAGAALVTVTGQAGFWMDTMLFGSFVLAGVGAGFVIIPFNSMLQRRTPEAYTGRVFGIVGSLTSAAVILGPVAGGALVTASGPATAFLVSGVLSALLGAAVLFLRTGIENRDQAAQELQQSAA
>NZ_LN831776.1|WP_020428240.1|783707_784175_-|MarR-family-transcriptional-regulator
MIQSYERDTQLTLHLYRVFAKSFKSINEHAVTGSKIEGFNPTAFAVMEVLYYKGPQPIQQIGAKLLLQSGNVTYVIDKLEERGYLQRKPCPSDRRVIFAELTSEGERLMNEMYPKYSERLHLAFSGLSDEEKEQMITLLKKMGLQAEKLSPLPRK
>NZ_LN831776.1|WP_020430610.1|796838_797447_-|superoxide-dismutase
MAFQLPALPYPNNALEPHIDALTMEIHHDRHHNTYVTNLNAALEKAPELQGKSIEELLTDLNAVPEAIRTAVRNNGGGHANHTLFWEVIGPNGGGAPTGALAAAIDSELGGFDKFKEDFATAATTRFGSGWAWLVVKDGKLAVTSTPNQDNPISEGATPILGLDVWEHAYYLNYQNKRPDYIKAFWNVVNWEEVGKRYESAK
>NZ_LN831776.1|WP_020430611.1|798035_798455_+|GNAT-family-N-acetyltransferase
MHVRSFQLSDVTSVTELLQTALSEECFESTIEPFSRQLSWDSDLIVVAEDEGEIVGALIGTIEKNHGCYFRIAVHPEYRRRGIGRGLVSAMEHKFQARKVSGIYVAVDEHNSFALPLYEAMGYNENQIFKSVRKLSIVG
>NZ_LN831776.1|WP_020430612.1|798696_799314_+|signal-peptidase-I
MNRELEEDFMRSRKHRYRSVTHRRTGSLSGTGWVRDLRDWLVTAAIVFALMSLLNIFVFNVSTVIGQSMQPTLFEGEKLIISKISLTFASPRRSDVVVLHDPSTGPDRKEYLVKRVIGIPGDRIEVRNHKLYVNGKLIGESYVDTEIQDPDFAELTVKQGTYFVMGDNRHAGASKDSRYFGAVPQNRIVGKAAYIWWPLSKANAL
>NZ_LN831776.1|WP_020430613.1|799332_800550_+|tRNA-epoxyqueuosine(34)-reductase-QueG
MNNNIQTAYAPPPSKWEGLKAEIKAAAPGIGIDDIGFATAEPFLYLKNILQEHRDNGYDSGFEEPDLDKRTIPALQSGGQPQSIIAIAVAYPSKMENPPKSEPGARRGILARASWGRDYHHVLREALAKLEAFIRERVPGAELESMVDTGVLVDRAVAERAGIGFSGKNCSIISPEWGSWIYLGEMVTNIPFPPDTPVEEGCGSCTKCIDACPTGALVGPGQLNAQACISYLTQTKGFLSEEYMTKIGNRLYGCDTCQIVCPKNRGKNWNHRPELLPDPEVVKPLLLPILELSNREFKEQFGSSSAAWRGKKPIQRNAVIALGNFKEAGAVPKLTEIVLKETRPELRGSAAWALGRIGGAEALAAVKLALHKEEDATVREMLERAQGKLLERGEAEGQDGASGQG
>NZ_LN831776.1|WP_020430614.1|800653_800905_+|YneF-family-protein
MNIALPIITLVVGLVGGFFIGVYYLRRQMTAMQNDPEMLQKVAKQMGYNLNGKQMQRAQQMMKNGNQPGRAPAAGKRQGRKGK
>NZ_LN831776.1|WP_020430615.1|800955_801549_+|GTP-cyclohydrolase-I-FolE
MGGVKDYMNGKVAANREQIEYHVEKILQLIGEDPGREGLLETPARVTRMYEEIFGGYSIDPREALGVTFDESHEELVIVKDIVYYSQCEHHMAPFFGKVHIGYIPSGRIAGLSKLARLVEAVSRRLQVQERITAQIADIMTEVLNPHGVMVVVEGEHLCMCARGVKKPGSKTVTMAARGTFREDAAARAEFLALIKE
>NZ_LN831776.1|WP_020430616.1|801658_802837_-|DUF2935-domain-containing-protein
MPDQYGQVLPVRILEEIAFWKKQEQEHTEVIKGVVPQLEKPYVKLLDEWAVVFEATGAATRQLMEASRASSPAELAAGTEQLLQVACSQSREFIRQQHALMEESAAVKAQPLAGAVLLHIIRESEYVEALLNTLSVPGIAPGWTRESAAPLPETADELNARDKKAKHEPQAPMASPLSGQQEPGTVPIGGHTLPPLPYAYNALEPYIDEKTMRIHHDKHHQSYVDGLNKAENKLAEARKTKDFDLVKHWERELAFNGAGHYLHTIFWNVMSPQGGGRPTGPLLDAIEHSFGSYDAFKEQFTEAANKVEGGGWAILVWSPRSRRLEILTAEKHQNLSQWDVVPLLALDVWEHAYYLKHQNNRADYIKDWWKVVHWPYVSERFNAARKLVWQPF
>NZ_LN831776.1|WP_020430617.1|802918_805165_-|hypothetical-protein
MKLSTNTAGQTSGILDDMKIFVSRDENRGISFTNKEAAYYYTQSHLNDHVEHAYFAGLNISKSRIFSGYTLIADQQKLDNQEAEVCVYPYKMVRMHGSLTEELWMFDYKNVLEISLTGAQETIGIEILGEQLNLLNSRDGIAFFNSIEGGWVIAVGAAGNQPVEVKNHTVYSAANAGGFYIAVGKTVAEAADMIHDTRRDAVSMKHERMKRMEDFLQKNVYIASSSDSLALSLNWLNITMDQLVTRQQGDGIYAGLPWFNEYWGRDQFIALPGAVLVTGQFETAKNILLSFAKFQNTDAASKYFGRVPNILALKNVDYHTTDGTPRFIIQLQDYVKYSGDTAVITELYPAVQNSIEGSIKHWVDDKGYLMHDDNETWMDARDANLKSYSPRDTRANDIQALWYNQLQAGVYFAEYMGDSGSAKKWGNIASKLKRNFAADFRDQTHPYLADRLNPEDEPEFSLRPNQLFALDMIDDDSFKCEVIKTAWEELVYPWGVASLDQKHPFFHPFHLTSLYHKDEAYHNGTVWLWLNGIAMQRMIEAGQEETAYKLFKNMNWQALNLGVVGGLSENMDAYPQEGQSWAKLTGAYLQAWSNAEQLRVWYQYFLGFRPDMIHQALTLAPRIPEEIRDLQARVKIGSGTIDFTYTATAATEQTYLYGFKGIGLTAVIDISPFKILQIEAEKDCELKITRTELKLTAVLSDKTGTTGKEIIVSRLPLREEQQLNVKQVFQHVKFAEPMGLENHPVTKR
>NZ_LN831776.1|WP_039790050.1|805198_806077_-|carbohydrate-ABC-transporter-permease
MYTHSVKSRIADTIIWILVLAFTLSCLIPLINLVAISFSDNAAASANMVSIFPVNFTLSSYEKLVSDSQFWRSFMISVERVVLGLIVNMMLMILAAYPLSKSSKQFRAQKVYMNIVIFAMLFSGGLIPTFMVVKGLHLLDSIWALILPGAVPIANVILLMNAFRAVPKSLEEAATIDGASQWRILSTIYVPVVLPTLATVTLFTIVGHWNDYFSALVYINKTSNYPLQTYIQQLSVDVQNITDPQKLIEYSKISNRTLNAAKIVISTLPLLLIYPFMQKYFVTGIVVGSVKE
>NZ_LN831776.1|WP_020430620.1|806094_806985_-|sugar-ABC-transporter-permease
MNNKKDQAAFHLMLAPSIVFLIIFSFIPMFGIVMAFQNYIPAKGISDSAWVGLDNFKFMFQIPDSRQILVNTIVIALWKIIVGTIVSIVFALLLNEIRVRFAKKFMQTVVYLPNFLSWAVLATVVMNIFSYEGPVNAFLGWLGIDPVLFMASNHWFRPMLVLTDVWKGFGYGSIIYLASLTAIDPGLYEASSIDGANRFKQLWHITLPGLMPTILLVTTLNLPNVLNAGFDQIFNLYNPLVYATSDIIDTYVYRVGLVERQYSLGTAIGLLRSVVGIVLILSANKLAQKLTDYRIF

Crispr_ID: NZ_LN831776_12

• CRISPR_ID: NZ_LN831776_12
• CRISPR_location: 819847-819923
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_12

Consensus_repeat	Method
TAAGTGGAAAAAGGGAACTTAAATTC	CRISPRCasFinder

spacers of NZ_LN831776_12

>12.1|819873|25|NZ_LN831776|CRISPRCasFinder
CTCAGAAATCAACAATTGTGAGGTT

CRISPR arrays and Neighbor proteins around NZ_LN831776_12

CRISPR arrays

The CRISPR arrays of NZ_LN831776_12

>merge|NZ_LN831776|12|819847-819923|CRISPRCasFinder
TAAGTGGAAAAAGGGAACTTAAATTCCTCAGAAATCAACAATTGTGAGGTTTAAGTGGAAAAAGGGAACTTAATTCA

>NZ_LN831776|12|12|819847-819923|CRISPRCasFinder
TAAGTGGAAAAAGGGAACTTAAATTC	CTCAGAAATCAACAATTGTGAGGTT
TAAGTGGAAAAAGGGAACTTAATTCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020430639.1|825215_825485_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020430638.1|824313_825198_+|inositol-monophosphatase	unknown	unknown	gnl|CDD|238817
NZ_LN831776.1|WP_020430648.1|828492_829113_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020430620.1|806094_806985_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_LN831776.1|WP_020430636.1|822777_823095_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046501134.1|813528_814272_+|IclR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224332
NZ_LN831776.1|WP_039790050.1|805198_806077_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_046501132.1|808991_810512_+|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_039790066.1|826936_827545_+|peptide-deformylase	unknown	unknown	gnl|CDD|234668
NZ_LN831776.1|WP_141639159.1|816242_816605_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197715
NZ_LN831776.1|WP_046501137.1|825582_826878_+|copper-amine-oxidase	unknown	unknown	gnl|CDD|377924
NZ_LN831776.1|WP_020430633.1|816771_819516_-|aconitate-hydratase-AcnA	unknown	unknown	gnl|CDD|236445
NZ_LN831776.1|WP_020430637.1|823091_824099_+|UV-DNA-damage-repair-endonuclease-UvsE	unknown	unknown	gnl|CDD|235029
NZ_LN831776.1|WP_039790056.1|812283_813252_-|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|224423
NZ_LN831776.1|WP_020430625.1|810533_812243_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_020430650.1|829228_830545_-|glutamate-1-semialdehyde-2,1-aminomutase	unknown	unknown	gnl|CDD|183493
NZ_LN831776.1|WP_039790060.1|820589_821618_+|amidase-domain-containing-protein	unknown	unknown	gnl|CDD|378910
NZ_LN831776.1|WP_020430621.1|807004_808723_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270298
NZ_LN831776.1|WP_020430635.1|821637_822729_+|D-alanine--D-alanine-ligase	unknown	unknown	gnl|CDD|234993
NZ_LN831776.1|WP_020430617.1|802918_805165_-|hypothetical-protein	unknown	unknown	gnl|CDD|283786

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020430638.1|824313_825198_+|inositol-monophosphatase	gnl|CDD|238817	cd01639, IMPase, IMPase, inositol monophosphatase and related domains. A family of Mg++ dependent phosphatases, inhibited by lithium, many of which may act on inositol monophosphate substrate. They dephosphorylate inositol phosphate to generate inositol, which may be recycled into inositol lipids; in eukaryotes IMPase plays a vital role in intracellular signaling. IMPase is one of the proposed targets of Li+ therapy in manic-depressive illness. This family contains some bacterial members of the inositol monophosphatase family classified as SuhB-like. E. coli SuhB has been suggested to participate in posstranscriptional control of gene expression, and its inositol monophosphatase activity doesn't appear to be sufficient for its cellular function. It has been proposed, that SuhB plays a role in the biosynthesis of phosphatidylinositol in mycobacteria.	1.02382e-107
NZ_LN831776.1|WP_020430620.1|806094_806985_-|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	4.79663e-113
NZ_LN831776.1|WP_046501134.1|813528_814272_+|IclR-family-transcriptional-regulator	gnl|CDD|224332	COG1414, IclR, Transcriptional regulator [Transcription].	1.1397e-54
NZ_LN831776.1|WP_039790050.1|805198_806077_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	5.2004e-57
NZ_LN831776.1|WP_046501132.1|808991_810512_+|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	9.1375e-46
NZ_LN831776.1|WP_039790066.1|826936_827545_+|peptide-deformylase	gnl|CDD|234668	PRK00150, def, peptide deformylase; Reviewed.	4.70083e-57
NZ_LN831776.1|WP_141639159.1|816242_816605_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|197715	smart00421, HTH_LUXR, helix_turn_helix, Lux Regulon. lux regulon (activates the bioluminescence operon.	2.40013e-20
NZ_LN831776.1|WP_046501137.1|825582_826878_+|copper-amine-oxidase	gnl|CDD|377924	pfam07833, Cu_amine_oxidN1, Copper amine oxidase N-terminal domain. Copper amine oxidases catalyze the oxidative deamination of primary amines to the corresponding aldehydes, while reducing molecular oxygen to hydrogen peroxide. These enzymes are dimers of identical subunits, each comprising four domains. The N-terminal domain, which is absent in some amine oxidases, consists of a five-stranded antiparallel beta sheet twisted around an alpha helix. The D1 domains from the two subunits comprise the 'stalk' of the mushroom-shaped dimer, and interact with each other but do not pack tightly against each other.	1.07641e-20
NZ_LN831776.1|WP_020430633.1|816771_819516_-|aconitate-hydratase-AcnA	gnl|CDD|236445	PRK09277, PRK09277, aconitate hydratase AcnA.	0
NZ_LN831776.1|WP_020430637.1|823091_824099_+|UV-DNA-damage-repair-endonuclease-UvsE	gnl|CDD|235029	PRK02308, uvsE, putative UV damage endonuclease; Provisional.	1.60943e-126
NZ_LN831776.1|WP_039790056.1|812283_813252_-|alpha/beta-fold-hydrolase	gnl|CDD|224423	COG1506, DAP2, Dipeptidyl aminopeptidases/acylaminoacyl-peptidases [Amino acid transport and metabolism].	1.14189e-11
NZ_LN831776.1|WP_020430625.1|810533_812243_+|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	2.64273e-50
NZ_LN831776.1|WP_020430650.1|829228_830545_-|glutamate-1-semialdehyde-2,1-aminomutase	gnl|CDD|183493	PRK12389, PRK12389, glutamate-1-semialdehyde aminotransferase; Provisional.	0
NZ_LN831776.1|WP_039790060.1|820589_821618_+|amidase-domain-containing-protein	gnl|CDD|378910	pfam12671, Amidase_6, Putative amidase domain.	8.24074e-39
NZ_LN831776.1|WP_020430621.1|807004_808723_-|extracellular-solute-binding-protein	gnl|CDD|270298	cd13580, PBP2_AlgQ_like_1, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	5.56046e-106
NZ_LN831776.1|WP_020430635.1|821637_822729_+|D-alanine--D-alanine-ligase	gnl|CDD|234993	PRK01966, ddl, D-alanine--D-alanine ligase.	1.05043e-168
NZ_LN831776.1|WP_020430617.1|802918_805165_-|hypothetical-protein	gnl|CDD|283786	pfam06202, GDE_C, Amylo-alpha-1,6-glucosidase. This family includes human glycogen branching enzyme AGL. This enzyme contains a number of distinct catalytic activities. It has been shown for the yeast homolog GDB1 that mutations in this region disrupt the enzymes Amylo-alpha-1,6-glucosidase (EC:3.2.1.33).	7.09693e-83

Protein sequences

>NZ_LN831776.1|WP_020430633.1|816771_819516_-|aconitate-hydratase-AcnA
MPSKDHFSLARTLESGGKSYRYYHLNSLEEQGAGDISSLPFSIKVLLEAAVRQYDGRAITEEHVKQLAGWSGGIDRNKEIPFIPARIVLQDFTGVPVVVDLAAMRDTVKKAGGDPKKINPLVPVDLVIDHSVMVDAFGTADALEYNMNVEFERNEERYRFLRWAQTAFNNFRAVPPATGIVHQVNLEYLASVAATKTSDGETVVYPDSLVGTDSHTTMINGLGVVGWGVGGIEAEAGMLGQPLYFVTPDVVGFKLTGSLVEGATATDLALTVTQMLRKKGVVGKFVEFYGPGLANISLADRATVANMAPEYGATIGFFPVDDETLAYLRSTGRPDELVELVGDYYKAQGMFRTSDTPDPTFTDTIELDLASVVPSLAGPKRPQDRVELTHMKENFEGIIRTPVDKGGYGLSDDKINEVVEVQHKNGTTSKLSTGAVVIAAITSCTNTSNPSVMLGAGLLAKKAVERGLTKPGYVKSSLTPGSLVVTEYLEKADLLKPLEALGFYLAGYGCATCIGNSGPLPDEVSQAITDNDMTVAAVISGNRNFEGRVHAQVKANYLASPPLVVAYALAGTVNIDLKTEPLGYDPQGEPVYLADIWPTSAEIREAIGLSLSPEMFRRKYENVFTANERWNSIPVPEGELYEWDDNSTYIQNPPFFENLADGVGDIKDIRNARVLALLADSVTTDHISPAGNISTSGPAGEYLRSHGVERADFNSYGSRRGNHEVMMRGTFANIRIRNAVAPGTEGGVTTFLPSEEVMSIYDASMLYQSAGQNLIVIAGKEYGTGSSRDWAAKGTLLLGVKAVIAESFERIHRSNLVGMGVLPLQFQEGHGWSSLGLTGRETFNITGLGNDVQPGQELAVTATREDGTQFEFPVIARLDSTVDIDYYRNGGILQTVLRQMLADATTSDSALPVE
>NZ_LN831776.1|WP_141639159.1|816242_816605_+|helix-turn-helix-transcriptional-regulator
MVCNVQAAINEELLASFQSFILSRSGDQQQEQAVSPGKLLNSAALKSPKEEWGISPREEEVLELIILGKTNKEIASALFISEHTVKNHLSRIFNKMNVTDRSQIIALIYKRILNSEGLEI
>NZ_LN831776.1|WP_046501134.1|813528_814272_+|IclR-family-transcriptional-regulator
MEDRKLTVRAVERALDILLCFTQENDLSLTEIASKISLHKSTVHRLLTTLEEKGFLLRNEATEKYRLGIRIWELSTHLPTLDEPAALLLPAMEKLRDRLGETVSLYLRDDLERVRIQAVQSRQAIRRVAQIGARLPLSVGASSKVLAAYAPQEVQTRLLADPNWPEAVDKGAYLGQLQEIIRRGYATSFEEREPGAAAVAVPIVGRAGTVAAALSLSGPVSRLSREMLEDYAVVLAENAAEMGLMMG
>NZ_LN831776.1|WP_039790056.1|812283_813252_-|alpha/beta-fold-hydrolase
MPGEHKPNAAPKLSLRMIRVKHIIVALLLSVFFFFVFCFIALHGYIAWVLSNPTVAPLYSNPSMAKGLDYEDITFPALDGSRMMQGWYIPSKGSSKTIVFSHGYGANREETWVPMYDLAHYAHSLNFNVVMFDYGFASKTNKDIATGGKKESQQLLGAIRYAKEHGAKEIVVWGFSMGAGTALQAGLVTKDVDAMILDSTFLLEPDTLYHNIKQNIDLPRQPSLEIMELLFPVLNGTGLNQIPYTKVKAEDYPFPTLFLHGTNDDKAPYPIAEELAANQSNPYSDSWIVKGSHHELLFREHPREYLRRVSAFLGNVQLAKAR
>NZ_LN831776.1|WP_020430625.1|810533_812243_+|sensor-histidine-kinase
MQTWKAFKQKIGDFRFQTKIKLSFLLVSMIPVIVLGSFCFSETRSLLVQQSKADLNATLQQSVLAVNNQLDVYNKVMNFLSFNQEIVNAANTTYTSAYEMYDQLNNVIDQNFFTARYLNTGVKQIILYTGTNLPPHGNTVRPIDEIKEASWYPHVMKSVDVLWFSSGRSVYSARRILSTKQENPKDNILFALVDYDALFKTFEPLESHGAEIVITDSNGNSIYSSGADRTNSGIPISDKEADELHWSGKNYTVLQSSIPITGWKVYLYKPTSLITKSAWWIALTVLLMIAACIAAVVVAGTLFSRKIMLPIHRLHKNMKLIGEGNLEIKVFSDSKDEIGDLIRGFGSMLGRTKTLIDTVYVGEIARKEYEMKALQAQINPHFLYNSLSLINWRAIRIHATDISEMAQLLSTFYRTTLNKGENLISVSDEILNVQSYINIQLIMHSNSFEIDYQIDDSILSCRMPNLMLQPLIENAIIHGIENREDGGGIIHLSGKKEDQSIVFLITDNGIGVEQERLALLLKSQSKGYGLKNVNDRAVVMYGEQYGLTINSIPGEGTQVLLKIPYDEHN
>NZ_LN831776.1|WP_046501132.1|808991_810512_+|response-regulator
MLTILIADDQREEREGIEFLIRELGFFLHIETAENGRKALEYLEKNPVDILFTDVRMPIMDGLQLTTEALTLQPKLKVILFSGFAEFEYAKTAISLGVSEYLLKPINVEAFRNTMQKVIAQLTDQEQEHIAAQIKLEYVKKHVLFNLVNGLGIPPSMKEISFELPDRYHGMFLLEFDKNFFENAGPEFEEFILSLLEDPVDYVNLNGCQSLLLFPGLPAVSSCSFRDLGAHLHDSILDKYKVHCYLAINDEFTMLQDLSAALIQLDQLMEYRFFSPDHFVFEVKKDVYFANDMLPGLSDYELLDHIRNNLKERDIFSLRANTDLLYQKYANQAQFSQLYVKYMFSSLYQEIMTYSAPISEMELSHGIEKIYKSEELKEIKEIIIAGITLLDREYNSSEFLNRDIAAVKQYIEDHYGEDLSLDLLAAKIHLSPHYLSSIFKKNTGCGLNKYIKNVRMNIAKDMLQQTHLKVSDICYSVGFQNVSYFCQNFRDFFGQTPEKFRQYNQK
>NZ_LN831776.1|WP_020430621.1|807004_808723_-|extracellular-solute-binding-protein
MSSKITKSCSIVLTALLAVSVAGCQSSNSNNDSAKSPAVDSNDPAWKEAQTSPYTPYPETVTYSIGQVASNFSALAGTPYEKDNATDNVWTRYFKEKLNVQNKVAFEANDGTDYNQKVSMAIVGGTIPDIMVVPDLSTLQQLYENDLIADLTDAYNQCASDQIKEIYDSYKGRVLDTARFDGKLMALPTTEISHGPGVLWLRKDWMDKLGLAEPKTMEDVENIITQFVEKDPGGNGAGNTVGLVVDNENTAGVSGGQYELNNIFTLYGAFPKQWMDDGSGKAVYGSVQPEMKPALAKLADMYKKGLIDKQFAVRTADDRKALLTSGKSGSFMDNWWGSWTVADSIKLNPNAKWVSYVAPQSEDGSVTMFTGNPSSSYLVVRKGFEHPEAAIKISSLQFDYQRYQEKDEAVLKKFEDYASLNVGGSPIAINIDYYDAFYRNVGIMEEALKTGDSSKLLTSNDRNAYRSYKKYLDNVKNGEKLDSNGWAGYTSSITTANLVKNSKIKEVNPVFFGTTPSMALKWPTLTKMELEMFLKIITGEQSPDAFDSFVSSWKKTGGDTITNEVNEAITSK
>NZ_LN831776.1|WP_020430620.1|806094_806985_-|sugar-ABC-transporter-permease
MNNKKDQAAFHLMLAPSIVFLIIFSFIPMFGIVMAFQNYIPAKGISDSAWVGLDNFKFMFQIPDSRQILVNTIVIALWKIIVGTIVSIVFALLLNEIRVRFAKKFMQTVVYLPNFLSWAVLATVVMNIFSYEGPVNAFLGWLGIDPVLFMASNHWFRPMLVLTDVWKGFGYGSIIYLASLTAIDPGLYEASSIDGANRFKQLWHITLPGLMPTILLVTTLNLPNVLNAGFDQIFNLYNPLVYATSDIIDTYVYRVGLVERQYSLGTAIGLLRSVVGIVLILSANKLAQKLTDYRIF
>NZ_LN831776.1|WP_039790050.1|805198_806077_-|carbohydrate-ABC-transporter-permease
MYTHSVKSRIADTIIWILVLAFTLSCLIPLINLVAISFSDNAAASANMVSIFPVNFTLSSYEKLVSDSQFWRSFMISVERVVLGLIVNMMLMILAAYPLSKSSKQFRAQKVYMNIVIFAMLFSGGLIPTFMVVKGLHLLDSIWALILPGAVPIANVILLMNAFRAVPKSLEEAATIDGASQWRILSTIYVPVVLPTLATVTLFTIVGHWNDYFSALVYINKTSNYPLQTYIQQLSVDVQNITDPQKLIEYSKISNRTLNAAKIVISTLPLLLIYPFMQKYFVTGIVVGSVKE
>NZ_LN831776.1|WP_020430617.1|802918_805165_-|hypothetical-protein
MKLSTNTAGQTSGILDDMKIFVSRDENRGISFTNKEAAYYYTQSHLNDHVEHAYFAGLNISKSRIFSGYTLIADQQKLDNQEAEVCVYPYKMVRMHGSLTEELWMFDYKNVLEISLTGAQETIGIEILGEQLNLLNSRDGIAFFNSIEGGWVIAVGAAGNQPVEVKNHTVYSAANAGGFYIAVGKTVAEAADMIHDTRRDAVSMKHERMKRMEDFLQKNVYIASSSDSLALSLNWLNITMDQLVTRQQGDGIYAGLPWFNEYWGRDQFIALPGAVLVTGQFETAKNILLSFAKFQNTDAASKYFGRVPNILALKNVDYHTTDGTPRFIIQLQDYVKYSGDTAVITELYPAVQNSIEGSIKHWVDDKGYLMHDDNETWMDARDANLKSYSPRDTRANDIQALWYNQLQAGVYFAEYMGDSGSAKKWGNIASKLKRNFAADFRDQTHPYLADRLNPEDEPEFSLRPNQLFALDMIDDDSFKCEVIKTAWEELVYPWGVASLDQKHPFFHPFHLTSLYHKDEAYHNGTVWLWLNGIAMQRMIEAGQEETAYKLFKNMNWQALNLGVVGGLSENMDAYPQEGQSWAKLTGAYLQAWSNAEQLRVWYQYFLGFRPDMIHQALTLAPRIPEEIRDLQARVKIGSGTIDFTYTATAATEQTYLYGFKGIGLTAVIDISPFKILQIEAEKDCELKITRTELKLTAVLSDKTGTTGKEIIVSRLPLREEQQLNVKQVFQHVKFAEPMGLENHPVTKR
>NZ_LN831776.1|WP_039790060.1|820589_821618_+|amidase-domain-containing-protein
MEQQWKQSLYGYVDQVNKGRVAPGAEQQRSTVRDPRFLLEQGERSRRLTQWYERRGITPLRSETGVRTLRTIRQNPSEVVADVALHNALYYEKGGITHREDVIESERLTFVLEGSTWEIAAVERSVPERNSMGRVAEAEPALRLSKWGEALPVPQPSQPLLNKDILRSITGSKEVRYRREDAAAYADRWWKDGNPEFEVFDVDCTNYVSQCLFAGGAPINYTGKRETGWWYKGYNGAQEWWSFSWAVSDSLQRYLSAGRSSGLRAETVERADQLMLGDIIQYDWDGNGHYQHSTIVTAFDAAGQPLVNARTVSSRHRFWDYRDSYAWTDRTAYRFFHINDYL
>NZ_LN831776.1|WP_020430635.1|821637_822729_+|D-alanine--D-alanine-ligase
MGDTKITVGLVYGGKSGEHEVSLQTAFAVMNAFDYAKYEIIPFYISKQGLWKVGAAMDAPFGTIQELKLGGEAGDMSMALNAVFSGLTGGDQLIDVMFPLLHGTNGEDGTIQGLFEMANIPYIGAGVLASSAGMDKVVMKKLFGEAGLDQCEYCYFNISAWKRKSHELIISLEDKLGYPVFVKPANLGSSVGISKAVDKESLIKAVEVAFRYDTKVIIEEFVDAREVEVSVLGNEEPEASVPGEIVSSGEYYDYAAKYTDGKSQMLIPAPVDPEVADRLRESAIQAFRAIEGSGITRADFFLRKSDGKILINEVNTMPGFTPYSMYPLLWRETGVSYQALLDRMIELALERYHFKQNLKYDNE
>NZ_LN831776.1|WP_020430636.1|822777_823095_+|hypothetical-protein
MGFQSEFNSVCKFKNDQELYELLEYGRTKMVKQGFRVYPTGQKVIAYTPENVAIAIVKISASIAEINFQGNEVTAVEMDLVRKLNEEESRVQTALASEMFFGEEG
>NZ_LN831776.1|WP_020430637.1|823091_824099_+|UV-DNA-damage-repair-endonuclease-UvsE
MIVRFGYVAMSTVIPDCSPSKTMTMASFNKLNDREAGLRRLEAIARGNLHNTLRLLKHNVGSDIRVYRLTSKLIPLATHPDLQDWNPFEALAADFAEAGSYVKKHGLRVSFHPDHFTVLSTPRPEVLASSVRDLQHHVDMLNAMDLPATAKNNIHIGGAYGDKPAAAARFLEHFAELPLDLQERTTLENDDKTFNAPETLEVSRRLGVPMVLDIHHQWVNNEGELPWELWPEIMKTWQTPLALKDVLPGETLPPKIHVSSPRSPSDPRSHADGVEPAPLLAFLKRIAADTPAVDAMIEAKAKDGALFGLMEALKELAEAGNGITVLDGASVNIEP
>NZ_LN831776.1|WP_020430638.1|824313_825198_+|inositol-monophosphatase
MNPTNSDNRNDREPYVVTSKGHTAAAINAAAKAGEWIKNRQGRVKELGSKTSAQDLVTEVDKGVEQMIRRLILTHYPDHAILGEESVQPGADALTAALEEGRKHEYLWIVDPIDGTTNFVHGFPFYCVSIALVVKGELTVGVIYDPIRDEMFVAEKGKGAYMHGIPTSVSAEADPGSSLVAMGFPPDRTFAQPANMAGLQQILPQIRGIRAGGSAALHLAYVAAGRVDGYWEVGLSPWDCAAGVLLVLESGGKVTDTLGNPYDIGTRHVVASNGRIHDFLLASLGEAEATGYNK
>NZ_LN831776.1|WP_020430639.1|825215_825485_+|hypothetical-protein
MSEKDDLERKLSELLEDGELEEADRTAKEIRQISPKYEIRIQTTLDPIVEETLRYRKIGHELDDRYDKYLERAKKDHGSEDKDNTKQSF
>NZ_LN831776.1|WP_046501137.1|825582_826878_+|copper-amine-oxidase
MLNAWKKMYAAGTSSLLLFTLWISAGAGSASAAEAAAAVQGSEQEVFRIVALGDSITAGYEPGMTDPNVKPYGYAERLLEQGWYHGRSALSNYGILGLTTAGLLNYTAAIKDGAAATADGIQAGLPDPRINQFAALTPQIKTELSEADLITLTIGGNDVSSLLVTAKDLTEEAFKAQLDQLLASYSSNVKAALENIRAVNAKATILLADQYQPAPKIAVSSSYLKLMSAAQQFTATAESVAASLNQPDAPVKVAHVAESFAGVEASRTHIISAGAADFHPTQLGYETIAKVFAETYWGEYRVPSVSAWTAASAPMSIVVKGVELDTPNKPILKNGQNFLALKDILNAVGATGKWDNKTQSATIVYGGKTVVITIGSQTIKVNGAAAAIDTPAFLQKVGNEDKTYLPLAALATGLGFDVNYSSKLRTAFINP
>NZ_LN831776.1|WP_039790066.1|826936_827545_+|peptide-deformylase
MLLSSAKFKAEYTITMDDIVREGASVLRTVAEPVPIPLQAEDQEALQCMMQFLKNSQDPEVAAKYKLRSGVGLSANQIGLQKRMFVMYLRDEKGNMVEHAWVNPKVISHSVAMIYLPESEGCLSVDRPVHGFVPRYESVKVKGYNMTGKEVVMKFKGYQAIVVQHEIDHLDGIMFYDRINEENPFKLPQGVEIRSLYEQKSR
>NZ_LN831776.1|WP_020430648.1|828492_829113_+|hypothetical-protein
MGWSRVPIRGMQNVYNDEAKQIDEQILELFRQRKAVSGGKGLFPDTETIEEWATRFELQPDEITFILSSLNEARPRRKFWEEPGVLRGVLPIMQTTLQDDVEYTLTHALQHEKLSIVTLEIKYLKETVGQVSINPLLTLAVVGDTDYEIDGYGARGGGAHFHMQFMVWPPLPEDLSFVEFSLVPASNRFMCPIREEVFLDKQIDFH
>NZ_LN831776.1|WP_020430650.1|829228_830545_-|glutamate-1-semialdehyde-2,1-aminomutase
MNRTTSEHLYEEALQHIVGGVNSPSRSFKAVGGGAPVFMKRAGGSRFWDEDGNEYIDYLAAYGPIITGHAHPHITAAITQAAENGLLYGTPTQLEIKLAKMLKEAIPSMDKVRFVNSGTEAVMTTIRVARAYTKRSKIVKFAGCYHGHSDLVLVAAGSGPSTLGIPDSAGVPASIAQEVITVPFNDLDALREALDKWGADVAAVMVEPIVGNFGMVMPQPGFLEGLCKQAHDNGSLVIYDEVITAFRFHYGSTQTYAGLDHHEDIIPDLTALGKIIGGGLPIGAYGGRKHVMEQVAPLGPAYQAGTMAGNPASISAGIACLEVLAAEGVYDEMERLAIRLTEGLQASADRHGIPLTINRIRGAFSTHFCNHPVTNYDEAQDTDGGLFASFFRHMLNRGINLAPSKYEAWFLTTAHTDADIDATLEAAEASFRAMAAEK

Crispr_ID: NZ_LN831776_13

• CRISPR_ID: NZ_LN831776_13
• CRISPR_location: 828102-828179
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: WYL

Consensus repeat of NZ_LN831776_13

Consensus_repeat	Method
GAGCAGAATTAGTTAACCTTTTTCCAC	CRISPRCasFinder

spacers of NZ_LN831776_13

>13.1|828129|24|NZ_LN831776|CRISPRCasFinder
CTAATCTTCGGAGAACAGGGTTTT

CRISPR arrays and Neighbor proteins around NZ_LN831776_13

CRISPR arrays

The CRISPR arrays of NZ_LN831776_13

>merge|NZ_LN831776|13|828102-828179|CRISPRCasFinder
GAGCAGAATTAGTTAACCTTTTTCCACCTAATCTTCGGAGAACAGGGTTTTGGAGCAAATTAGTTAACCTTTTTCCAC

>NZ_LN831776|13|13|828102-828179|CRISPRCasFinder
GAGCAGAATTAGTTAACCTTTTTCCAC	CTAATCTTCGGAGAACAGGGTTTT
GGAGCAAATTAGTTAACCTTTTTCCAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020430639.1|825215_825485_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020430651.1|830709_831762_-|LCP-family-protein	unknown	unknown	gnl|CDD|224235
NZ_LN831776.1|WP_020430635.1|821637_822729_+|D-alanine--D-alanine-ligase	unknown	unknown	gnl|CDD|234993
NZ_LN831776.1|WP_020430636.1|822777_823095_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020430658.1|837790_838246_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_LN831776.1|WP_020430638.1|824313_825198_+|inositol-monophosphatase	unknown	unknown	gnl|CDD|238817
NZ_LN831776.1|WP_141639159.1|816242_816605_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197715
NZ_LN831776.1|WP_020430653.1|831864_832332_+|thioredoxin-dependent-thiol-peroxidase	unknown	unknown	gnl|CDD|224146
NZ_LN831776.1|WP_020430661.1|839985_840924_-|YafY-family-transcriptional-regulator	WYL	COG2378_WYL_CAS-I:CAS-III	gnl|CDD|225253
NZ_LN831776.1|WP_046501137.1|825582_826878_+|copper-amine-oxidase	unknown	unknown	gnl|CDD|377924
NZ_LN831776.1|WP_051010671.1|832451_836747_+|2-hydroxyacyl-CoA-dehydratase	unknown	unknown	gnl|CDD|224835
NZ_LN831776.1|WP_020430637.1|823091_824099_+|UV-DNA-damage-repair-endonuclease-UvsE	unknown	unknown	gnl|CDD|235029
NZ_LN831776.1|WP_020430657.1|836862_837549_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046501140.1|838242_839772_+|DHA2-family-efflux-MFS-transporter-permease-subunit	unknown	unknown	gnl|CDD|129794
NZ_LN831776.1|WP_020430650.1|829228_830545_-|glutamate-1-semialdehyde-2,1-aminomutase	unknown	unknown	gnl|CDD|183493
NZ_LN831776.1|WP_039790060.1|820589_821618_+|amidase-domain-containing-protein	unknown	unknown	gnl|CDD|378910
NZ_LN831776.1|WP_039790066.1|826936_827545_+|peptide-deformylase	unknown	unknown	gnl|CDD|234668
NZ_LN831776.1|WP_039790075.1|841076_842360_+|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_LN831776.1|WP_020430648.1|828492_829113_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020430633.1|816771_819516_-|aconitate-hydratase-AcnA	unknown	unknown	gnl|CDD|236445

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831776.1|WP_020430661.1|839985_840924_-|YafY-family-transcriptional-regulator	WYL	COG2378_WYL_CAS-I:CAS-III	9.1e-69	227.0	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020430651.1|830709_831762_-|LCP-family-protein	gnl|CDD|224235	COG1316, LytR, Transcriptional regulator [Transcription].	3.63078e-59
NZ_LN831776.1|WP_020430635.1|821637_822729_+|D-alanine--D-alanine-ligase	gnl|CDD|234993	PRK01966, ddl, D-alanine--D-alanine ligase.	1.05043e-168
NZ_LN831776.1|WP_020430638.1|824313_825198_+|inositol-monophosphatase	gnl|CDD|238817	cd01639, IMPase, IMPase, inositol monophosphatase and related domains. A family of Mg++ dependent phosphatases, inhibited by lithium, many of which may act on inositol monophosphate substrate. They dephosphorylate inositol phosphate to generate inositol, which may be recycled into inositol lipids; in eukaryotes IMPase plays a vital role in intracellular signaling. IMPase is one of the proposed targets of Li+ therapy in manic-depressive illness. This family contains some bacterial members of the inositol monophosphatase family classified as SuhB-like. E. coli SuhB has been suggested to participate in posstranscriptional control of gene expression, and its inositol monophosphatase activity doesn't appear to be sufficient for its cellular function. It has been proposed, that SuhB plays a role in the biosynthesis of phosphatidylinositol in mycobacteria.	1.02382e-107
NZ_LN831776.1|WP_141639159.1|816242_816605_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|197715	smart00421, HTH_LUXR, helix_turn_helix, Lux Regulon. lux regulon (activates the bioluminescence operon.	2.40013e-20
NZ_LN831776.1|WP_020430653.1|831864_832332_+|thioredoxin-dependent-thiol-peroxidase	gnl|CDD|224146	COG1225, Bcp, Peroxiredoxin [Posttranslational modification, protein turnover, chaperones].	1.6906e-82
NZ_LN831776.1|WP_020430661.1|839985_840924_-|YafY-family-transcriptional-regulator	gnl|CDD|225253	COG2378, COG2378, Predicted transcriptional regulator [Transcription].	5.72605e-68
NZ_LN831776.1|WP_046501137.1|825582_826878_+|copper-amine-oxidase	gnl|CDD|377924	pfam07833, Cu_amine_oxidN1, Copper amine oxidase N-terminal domain. Copper amine oxidases catalyze the oxidative deamination of primary amines to the corresponding aldehydes, while reducing molecular oxygen to hydrogen peroxide. These enzymes are dimers of identical subunits, each comprising four domains. The N-terminal domain, which is absent in some amine oxidases, consists of a five-stranded antiparallel beta sheet twisted around an alpha helix. The D1 domains from the two subunits comprise the 'stalk' of the mushroom-shaped dimer, and interact with each other but do not pack tightly against each other.	1.07641e-20
NZ_LN831776.1|WP_051010671.1|832451_836747_+|2-hydroxyacyl-CoA-dehydratase	gnl|CDD|224835	COG1924, COG1924, Activator of 2-hydroxyglutaryl-CoA dehydratase (HSP70-class ATPase domain) [Lipid metabolism].	7.15309e-143
NZ_LN831776.1|WP_020430637.1|823091_824099_+|UV-DNA-damage-repair-endonuclease-UvsE	gnl|CDD|235029	PRK02308, uvsE, putative UV damage endonuclease; Provisional.	1.60943e-126
NZ_LN831776.1|WP_020430658.1|837790_838246_+|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	1.03074e-16
NZ_LN831776.1|WP_046501140.1|838242_839772_+|DHA2-family-efflux-MFS-transporter-permease-subunit	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	1.84016e-113
NZ_LN831776.1|WP_020430650.1|829228_830545_-|glutamate-1-semialdehyde-2,1-aminomutase	gnl|CDD|183493	PRK12389, PRK12389, glutamate-1-semialdehyde aminotransferase; Provisional.	0
NZ_LN831776.1|WP_039790060.1|820589_821618_+|amidase-domain-containing-protein	gnl|CDD|378910	pfam12671, Amidase_6, Putative amidase domain.	8.24074e-39
NZ_LN831776.1|WP_020430633.1|816771_819516_-|aconitate-hydratase-AcnA	gnl|CDD|236445	PRK09277, PRK09277, aconitate hydratase AcnA.	0
NZ_LN831776.1|WP_039790075.1|841076_842360_+|MFS-transporter	gnl|CDD|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	8.47034e-42
NZ_LN831776.1|WP_039790066.1|826936_827545_+|peptide-deformylase	gnl|CDD|234668	PRK00150, def, peptide deformylase; Reviewed.	4.70083e-57

Protein sequences

>NZ_LN831776.1|WP_039790066.1|826936_827545_+|peptide-deformylase
MLLSSAKFKAEYTITMDDIVREGASVLRTVAEPVPIPLQAEDQEALQCMMQFLKNSQDPEVAAKYKLRSGVGLSANQIGLQKRMFVMYLRDEKGNMVEHAWVNPKVISHSVAMIYLPESEGCLSVDRPVHGFVPRYESVKVKGYNMTGKEVVMKFKGYQAIVVQHEIDHLDGIMFYDRINEENPFKLPQGVEIRSLYEQKSR
>NZ_LN831776.1|WP_046501137.1|825582_826878_+|copper-amine-oxidase
MLNAWKKMYAAGTSSLLLFTLWISAGAGSASAAEAAAAVQGSEQEVFRIVALGDSITAGYEPGMTDPNVKPYGYAERLLEQGWYHGRSALSNYGILGLTTAGLLNYTAAIKDGAAATADGIQAGLPDPRINQFAALTPQIKTELSEADLITLTIGGNDVSSLLVTAKDLTEEAFKAQLDQLLASYSSNVKAALENIRAVNAKATILLADQYQPAPKIAVSSSYLKLMSAAQQFTATAESVAASLNQPDAPVKVAHVAESFAGVEASRTHIISAGAADFHPTQLGYETIAKVFAETYWGEYRVPSVSAWTAASAPMSIVVKGVELDTPNKPILKNGQNFLALKDILNAVGATGKWDNKTQSATIVYGGKTVVITIGSQTIKVNGAAAAIDTPAFLQKVGNEDKTYLPLAALATGLGFDVNYSSKLRTAFINP
>NZ_LN831776.1|WP_020430639.1|825215_825485_+|hypothetical-protein
MSEKDDLERKLSELLEDGELEEADRTAKEIRQISPKYEIRIQTTLDPIVEETLRYRKIGHELDDRYDKYLERAKKDHGSEDKDNTKQSF
>NZ_LN831776.1|WP_020430638.1|824313_825198_+|inositol-monophosphatase
MNPTNSDNRNDREPYVVTSKGHTAAAINAAAKAGEWIKNRQGRVKELGSKTSAQDLVTEVDKGVEQMIRRLILTHYPDHAILGEESVQPGADALTAALEEGRKHEYLWIVDPIDGTTNFVHGFPFYCVSIALVVKGELTVGVIYDPIRDEMFVAEKGKGAYMHGIPTSVSAEADPGSSLVAMGFPPDRTFAQPANMAGLQQILPQIRGIRAGGSAALHLAYVAAGRVDGYWEVGLSPWDCAAGVLLVLESGGKVTDTLGNPYDIGTRHVVASNGRIHDFLLASLGEAEATGYNK
>NZ_LN831776.1|WP_020430637.1|823091_824099_+|UV-DNA-damage-repair-endonuclease-UvsE
MIVRFGYVAMSTVIPDCSPSKTMTMASFNKLNDREAGLRRLEAIARGNLHNTLRLLKHNVGSDIRVYRLTSKLIPLATHPDLQDWNPFEALAADFAEAGSYVKKHGLRVSFHPDHFTVLSTPRPEVLASSVRDLQHHVDMLNAMDLPATAKNNIHIGGAYGDKPAAAARFLEHFAELPLDLQERTTLENDDKTFNAPETLEVSRRLGVPMVLDIHHQWVNNEGELPWELWPEIMKTWQTPLALKDVLPGETLPPKIHVSSPRSPSDPRSHADGVEPAPLLAFLKRIAADTPAVDAMIEAKAKDGALFGLMEALKELAEAGNGITVLDGASVNIEP
>NZ_LN831776.1|WP_020430636.1|822777_823095_+|hypothetical-protein
MGFQSEFNSVCKFKNDQELYELLEYGRTKMVKQGFRVYPTGQKVIAYTPENVAIAIVKISASIAEINFQGNEVTAVEMDLVRKLNEEESRVQTALASEMFFGEEG
>NZ_LN831776.1|WP_020430635.1|821637_822729_+|D-alanine--D-alanine-ligase
MGDTKITVGLVYGGKSGEHEVSLQTAFAVMNAFDYAKYEIIPFYISKQGLWKVGAAMDAPFGTIQELKLGGEAGDMSMALNAVFSGLTGGDQLIDVMFPLLHGTNGEDGTIQGLFEMANIPYIGAGVLASSAGMDKVVMKKLFGEAGLDQCEYCYFNISAWKRKSHELIISLEDKLGYPVFVKPANLGSSVGISKAVDKESLIKAVEVAFRYDTKVIIEEFVDAREVEVSVLGNEEPEASVPGEIVSSGEYYDYAAKYTDGKSQMLIPAPVDPEVADRLRESAIQAFRAIEGSGITRADFFLRKSDGKILINEVNTMPGFTPYSMYPLLWRETGVSYQALLDRMIELALERYHFKQNLKYDNE
>NZ_LN831776.1|WP_039790060.1|820589_821618_+|amidase-domain-containing-protein
MEQQWKQSLYGYVDQVNKGRVAPGAEQQRSTVRDPRFLLEQGERSRRLTQWYERRGITPLRSETGVRTLRTIRQNPSEVVADVALHNALYYEKGGITHREDVIESERLTFVLEGSTWEIAAVERSVPERNSMGRVAEAEPALRLSKWGEALPVPQPSQPLLNKDILRSITGSKEVRYRREDAAAYADRWWKDGNPEFEVFDVDCTNYVSQCLFAGGAPINYTGKRETGWWYKGYNGAQEWWSFSWAVSDSLQRYLSAGRSSGLRAETVERADQLMLGDIIQYDWDGNGHYQHSTIVTAFDAAGQPLVNARTVSSRHRFWDYRDSYAWTDRTAYRFFHINDYL
>NZ_LN831776.1|WP_020430633.1|816771_819516_-|aconitate-hydratase-AcnA
MPSKDHFSLARTLESGGKSYRYYHLNSLEEQGAGDISSLPFSIKVLLEAAVRQYDGRAITEEHVKQLAGWSGGIDRNKEIPFIPARIVLQDFTGVPVVVDLAAMRDTVKKAGGDPKKINPLVPVDLVIDHSVMVDAFGTADALEYNMNVEFERNEERYRFLRWAQTAFNNFRAVPPATGIVHQVNLEYLASVAATKTSDGETVVYPDSLVGTDSHTTMINGLGVVGWGVGGIEAEAGMLGQPLYFVTPDVVGFKLTGSLVEGATATDLALTVTQMLRKKGVVGKFVEFYGPGLANISLADRATVANMAPEYGATIGFFPVDDETLAYLRSTGRPDELVELVGDYYKAQGMFRTSDTPDPTFTDTIELDLASVVPSLAGPKRPQDRVELTHMKENFEGIIRTPVDKGGYGLSDDKINEVVEVQHKNGTTSKLSTGAVVIAAITSCTNTSNPSVMLGAGLLAKKAVERGLTKPGYVKSSLTPGSLVVTEYLEKADLLKPLEALGFYLAGYGCATCIGNSGPLPDEVSQAITDNDMTVAAVISGNRNFEGRVHAQVKANYLASPPLVVAYALAGTVNIDLKTEPLGYDPQGEPVYLADIWPTSAEIREAIGLSLSPEMFRRKYENVFTANERWNSIPVPEGELYEWDDNSTYIQNPPFFENLADGVGDIKDIRNARVLALLADSVTTDHISPAGNISTSGPAGEYLRSHGVERADFNSYGSRRGNHEVMMRGTFANIRIRNAVAPGTEGGVTTFLPSEEVMSIYDASMLYQSAGQNLIVIAGKEYGTGSSRDWAAKGTLLLGVKAVIAESFERIHRSNLVGMGVLPLQFQEGHGWSSLGLTGRETFNITGLGNDVQPGQELAVTATREDGTQFEFPVIARLDSTVDIDYYRNGGILQTVLRQMLADATTSDSALPVE
>NZ_LN831776.1|WP_141639159.1|816242_816605_+|helix-turn-helix-transcriptional-regulator
MVCNVQAAINEELLASFQSFILSRSGDQQQEQAVSPGKLLNSAALKSPKEEWGISPREEEVLELIILGKTNKEIASALFISEHTVKNHLSRIFNKMNVTDRSQIIALIYKRILNSEGLEI
>NZ_LN831776.1|WP_020430648.1|828492_829113_+|hypothetical-protein
MGWSRVPIRGMQNVYNDEAKQIDEQILELFRQRKAVSGGKGLFPDTETIEEWATRFELQPDEITFILSSLNEARPRRKFWEEPGVLRGVLPIMQTTLQDDVEYTLTHALQHEKLSIVTLEIKYLKETVGQVSINPLLTLAVVGDTDYEIDGYGARGGGAHFHMQFMVWPPLPEDLSFVEFSLVPASNRFMCPIREEVFLDKQIDFH
>NZ_LN831776.1|WP_020430650.1|829228_830545_-|glutamate-1-semialdehyde-2,1-aminomutase
MNRTTSEHLYEEALQHIVGGVNSPSRSFKAVGGGAPVFMKRAGGSRFWDEDGNEYIDYLAAYGPIITGHAHPHITAAITQAAENGLLYGTPTQLEIKLAKMLKEAIPSMDKVRFVNSGTEAVMTTIRVARAYTKRSKIVKFAGCYHGHSDLVLVAAGSGPSTLGIPDSAGVPASIAQEVITVPFNDLDALREALDKWGADVAAVMVEPIVGNFGMVMPQPGFLEGLCKQAHDNGSLVIYDEVITAFRFHYGSTQTYAGLDHHEDIIPDLTALGKIIGGGLPIGAYGGRKHVMEQVAPLGPAYQAGTMAGNPASISAGIACLEVLAAEGVYDEMERLAIRLTEGLQASADRHGIPLTINRIRGAFSTHFCNHPVTNYDEAQDTDGGLFASFFRHMLNRGINLAPSKYEAWFLTTAHTDADIDATLEAAEASFRAMAAEK
>NZ_LN831776.1|WP_020430651.1|830709_831762_-|LCP-family-protein
MPPRKKRHAKAGKSKKKPLLWTLAIILLLIIGGIVYYFAEIYNQMDNLHKTGEDSPFAAIPSPSAETVQPPKWEGTEPVNILLMGVDARGVKKGEVPRSDTMLVASLDPVKKKFYVFSILRDTYVSIPEHGKERINTAITHGPNTAMQTVSELLGIPIQYYVYTDFQGFIKLVDAVGGVDYEVEKDMVYKTKADGPEYDIDLKKGFQHLDGSMALQYVRFRHDATSDFTRTERQRGFLKAVADKVISTTSIIKLPNILSQVTPYIDTNLDVNDMWKLATVGYDSSMGGSAQIPPMNLLTEEKTSGGSAVLGISSENKLKKFVQDTLAGPEPSPSPDASPGSSPSASAGSK
>NZ_LN831776.1|WP_020430653.1|831864_832332_+|thioredoxin-dependent-thiol-peroxidase
MNKIEVGQEVPDFTLPASTGQNISLSDYRGRKVVLYFYPKNMTPACTQEACDFRDAGDPIARGNAVVLGISPDSLSSHAKFIEKHSLPFPLLSDEDHTVSQLFGVWQLKKLYGKEFMGIVRSTFLIDEQGILVKEWRKVRVKGHVEALLGEIMNK
>NZ_LN831776.1|WP_051010671.1|832451_836747_+|2-hydroxyacyl-CoA-dehydratase
MMMLRIGLDVGSTTAKLVVMEHDVIVYQDYVRHFSDIKKAALSLLSDVRDRFPDREAALTVSGSSGLSLSKLGEVPFVQEVIACTKAISELIPQCDTAIELGGEDAKIIYLSGGIEQRMNTACAGGTGAFIDQMASLLQTDPAGLNVLAEQHERIYPIASRCGVFAKSDVQPLLNEGARREDVAASIFQSIVNQTISGLACGRPIRGRVAFLGGPLTFLPALRERFAETLGLSDSDVLFPEHSQYFVAIGSALSQTDPLVLPLSGWMARLDAVDFSADRAEDAELQPLFASPEALEQFRLRHSRAAAPRSELDTYQGPCYLGIDAGSTTTKLVITGAADEILYTFYGSNKGNPLQSVSDALKEIYRILPEGCHIAGAYATGYGEGLVKAALRTDGGEVETVAHYKAASKFMPEVDFILDIGGQDMKCIKIRGGAIDSLMLNEACSAGCGSFLESFASALGLGIGEFAAAALESAQPVNLGSRCTVFMNSKVKQVQKEGATLADLSAGLAYSVIKNALQKVIKIRNADDLGRNIIVQGGTFYNEAVLRAFELLTGRTVVRPDIAGVMGAYGCALLAREHAGFDGVSTLLGPEELEAFKYEVSPGRCRLCANNCALTISRFPDKSFHVTGNRCERGAGGKKEKNNLPNLMQYKYERFFDYEGLPVEQAERGTVGIPRTMNMFENYPFWHTFFTTLRYRTVLSPKSSKKLYESGMDTIPSESICYPAKMAHGHVQSLLGKGVDFIFYPAVVYEKKEDDAAQNHFNCPVVASYPEVIRNNMDGLKEKNIPLVSPFLTFDDIPALTRVLVKTFMDIPKEEIAAAVQTGLAEAERAKADLRNKGEETLEFLTHSGTKGILLCGHPYHADPEINHGIAEMITGMGLAVLTEDSICHLDRSEGEVGVVNQWTYHARMYRAARLAASRNDLELVQLTSFGCGIDAITCDAVQEILERNNKVYTLIKIDEISNLGAARIRLRSLLAAMREREKGDVKPQLLYKTQANMPFTKEMKETYTILAPQMSPIHFELFERVFRDAGYRLKILESTGPKETEEGLRYVNNDACYPAIVTIGQMLSALKSGDYDPDRTAVIMSQTGGGCRATNYISLLRKALKDSGLGQIPVISLNASGMENQPGFRISLRLANRLIAAACYGDLMMRLLHRFRPYEVIPGSAQALFRKGMDRCKSSLSTFSFREYKRLTREIVAEFVQLPVIKTVKPQVGIVGEILIKFHPDANNHIIEMIEAEGGEAVMPDFLDFIFYCVYNPIYKAEQFGKSKKLGFFNPMLISYLEIYRKPVKAALEEAGLAKGRENIYGLAEKASRLVSVGNQMGEGWFLTAEMMDLLDNGVNNIACIQPFACLPNHITGRGMIKGLKDLYPGANIAAIDYDAGVSVVNQANRIKLMMSIASGLTSSTPSSGAKVKRGSAIKPVVVGSVRSDL
>NZ_LN831776.1|WP_020430657.1|836862_837549_-|hypothetical-protein
MSLEARKIWNAIHQQLTRIITKPEEHANAVALFLELHDCLYASNGNNPEQTNYEDELLKDLREQTMRSYPVHTANSNNSIVWHIWHSARIEDITMNILTADRDQILHSGHYADKLHTPFIHSGNGMSGQEIAEFSAAVDLEALLEYRQAVAAGTRSIIAGLQPGQFRNKPRSTQISRISAEGAVKETEQWLIDYWGGKTIAGLVLMPATRHNFVHLNKAMRVKLKLQK
>NZ_LN831776.1|WP_020430658.1|837790_838246_+|MarR-family-transcriptional-regulator
MLEDREQQLDDIFSSFRCIIHNFQQLMWKDAEKLNITSTQLMVLRKLEAHPDVGITELADLLHLGNSAASGVVDRMVKAGLITRQRSESDRRIFKLAMTDKGREIREQSKQSLRSHLEPLVNIPPEDARELLRLHREIITILEQGRENNKL
>NZ_LN831776.1|WP_046501140.1|838242_839772_+|DHA2-family-efflux-MFS-transporter-permease-subunit
MSTVTANAAGPSKTIRRGPIIAALLIGAFVALLNQTLMNVALPKMMEDLKIAANTAQWLTTGFMLVNGVLIPISAYLVEKFTTRQLFTTAMMLFSIGTLVCAIGTGFEMIMVGRVIQAVGAGILMPLMNIVFLRIFPIEERGKAMGLMAVAMIFAPAVGPTLSGWVVQNYSWRVLFYIVLPLAVFSTLLGMKTMQNVGKLTSPRLDKMGVVLSTLAFGGLLYGFSDAGTDGWNSATVYACLILGVVALALFVWRELKTDKPLLEFRIFRYNMYSLTTVINIIVTMALYSGMILLPIYLQTIRGFTPMESGLMLLPGAILMGVMSPITGIIFDKIGARWLSVIGLIITTITTWEFSQITHTTTYTHLILTYTARMFGMSMLMMPIVTAGLNQLPQRLASHGTAMSNTLRTVGGALGMALFVSLMTNRTKSDITEAVMSGSVSQTDKAAMLKLTQDATINGITHAFTVATWVTVVALVLALFIKKTSPQPDFLQTEDTEPVQPSKVKSQQA
>NZ_LN831776.1|WP_020430661.1|839985_840924_-|YafY-family-transcriptional-regulator
MKIDRLLSIVILLMNRPLVQAKELADMFEVSVRTIYRDIDSINGAGIPVVTYQGANGGIGLMEGYRLDRNVLTERELADIFTALQSVSSYGAGEHNLLMEKITSVIPPSKSHAFRSKTTQLIVDFSPWGLQGPLEERLSLLKEALDESTAVAFDYVNADGQISHRIVEPYTLVHKGAGWYLYGFCIQRQDFRLFKLLRMKSLVKEARSFERLDIPLQDLPWTEGWKEPLNTQTVVLHFSAEGRYLAEDYFDCEELEADGNGGYIVRLAYAENNWLYGFLLSFGTVVEVLEPEPVRRRLAGLAAEIAAKYKLL
>NZ_LN831776.1|WP_039790075.1|841076_842360_+|MFS-transporter
MNITENGPTEVLKRRSKGYSRLFAAGLVNGIGDRFSSVAMLALILQVTGSGMAVGISLGMRVLPFLFMAPLGGMLAGRLPRKTIMMAVDLLRVPVALSFLLVDGAGRLWLLYAGSFIMAAGEALYSPVRKSSIPLLAGPDSLHKINSLEQLMTGCVLILGAFTGGLVSLWWGPEMAFVANAASFLLAALLIWGISFPAAVSSGTELLEDSVPAKPVIQDSLKRTGRWQSLRVLIGGSQVLQIILAYELLVPVINGWDNVLISVYAVQVFHAGDVGVGAFYAALGTGLSLSFFAGRLLKRRLLGIALGGLLLEGILLMCISGSRHFGVAFVLYILLSLCGGIGSACLDTLVMRETPAAQQPVIFGILSALGGSLIGLSMFSAGWLLEVMEPRALGFGGGAGFAGAALLLGVLAWLLRYRRKMPRELRQ

Crispr_ID: NZ_LN831776_14

• CRISPR_ID: NZ_LN831776_14
• CRISPR_location: 1028380-1028456
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_14

Consensus_repeat	Method
AAACAACGGTAGAAATGCCGTTGTTG	CRISPRCasFinder

spacers of NZ_LN831776_14

>14.1|1028406|25|NZ_LN831776|CRISPRCasFinder
GAGCGCTGAAGGCCGGTTCGCCCGG

CRISPR arrays and Neighbor proteins around NZ_LN831776_14

CRISPR arrays

The CRISPR arrays of NZ_LN831776_14

>merge|NZ_LN831776|14|1028380-1028456|CRISPRCasFinder
AAACAACGGTAGAAATGCCGTTGTTGGAGCGCTGAAGGCCGGTTCGCCCGGAAACAACGGTAGAAATGCCGTTGTTG

>NZ_LN831776|14|14|1028380-1028456|CRISPRCasFinder
AAACAACGGTAGAAATGCCGTTGTTG	GAGCGCTGAAGGCCGGTTCGCCCGG
AAACAACGGTAGAAATGCCGTTGTTG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020430451.1|1041118_1042159_+|NAD(P)-dependent-alcohol-dehydrogenase	unknown	unknown	gnl|CDD|176188
NZ_LN831776.1|WP_167345579.1|1034657_1035848_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020430472.1|1025704_1026592_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_020430453.1|1039769_1040897_+|ROK-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224851
NZ_LN831776.1|WP_020430464.1|1028868_1029810_-|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_020430454.1|1039252_1039696_-|acetyltransferase	unknown	unknown	gnl|CDD|182510
NZ_LN831776.1|WP_020430487.1|1020241_1020610_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224647
NZ_LN831776.1|WP_020430448.1|1042742_1043381_+|glycoside-hydrolase-family-11-protein	unknown	unknown	gnl|CDD|366111
NZ_LN831776.1|WP_020430485.1|1020793_1022389_+|response-regulator	unknown	unknown	gnl|CDD|227095
NZ_LN831776.1|WP_081487245.1|1026648_1027419_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_039789981.1|1027459_1028341_+|family-43-glycosylhydrolase	unknown	unknown	gnl|CDD|350148
NZ_LN831776.1|WP_020430461.1|1031220_1033056_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020430459.1|1033031_1034591_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|275228
NZ_LN831776.1|WP_020430491.1|1018249_1019416_+|DUF4317-domain-containing-protein	unknown	unknown	gnl|CDD|379500
NZ_LN831776.1|WP_020430488.1|1019516_1020050_-|NAD(P)H-dependent-oxidoreductase	unknown	unknown	gnl|CDD|376808
NZ_LN831776.1|WP_020430483.1|1022391_1024152_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_020430492.1|1017120_1017855_+|hypothetical-protein	unknown	unknown	gnl|CDD|180688
NZ_LN831776.1|WP_020430463.1|1030005_1031037_+|rhamnogalacturonyl-hydrolase	unknown	unknown	gnl|CDD|226678
NZ_LN831776.1|WP_020430481.1|1024278_1025691_+|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_LN831776.1|WP_020430456.1|1035892_1039258_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020430451.1|1041118_1042159_+|NAD(P)-dependent-alcohol-dehydrogenase	gnl|CDD|176188	cd05285, sorbitol_DH, Sorbitol dehydrogenase. Sorbitol and aldose reductase are NAD(+) binding proteins of the polyol pathway, which interconverts glucose and fructose. Sorbitol dehydrogenase is tetrameric and has a single catalytic zinc per subunit. Aldose reductase catalyzes the NADP(H)-dependent conversion of glucose to sorbital, and SDH uses NAD(H) in the conversion of sorbitol to fructose. NAD(P)(H)-dependent oxidoreductases are the major enzymes in the interconversion of alcohols and aldehydes, or ketones. The medium chain alcohol dehydrogenase family (MDR) have a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The N-terminal region typically has an all-beta catalytic domain. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit.	1.11617e-175
NZ_LN831776.1|WP_020430472.1|1025704_1026592_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	4.90539e-83
NZ_LN831776.1|WP_020430453.1|1039769_1040897_+|ROK-family-transcriptional-regulator	gnl|CDD|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	1.34248e-44
NZ_LN831776.1|WP_020430464.1|1028868_1029810_-|AraC-family-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	7.61858e-27
NZ_LN831776.1|WP_020430454.1|1039252_1039696_-|acetyltransferase	gnl|CDD|182510	PRK10514, PRK10514, putative acetyltransferase; Provisional.	1.27512e-43
NZ_LN831776.1|WP_020430487.1|1020241_1020610_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	2.97536e-39
NZ_LN831776.1|WP_020430448.1|1042742_1043381_+|glycoside-hydrolase-family-11-protein	gnl|CDD|366111	pfam00457, Glyco_hydro_11, Glycosyl hydrolases family 11.	4.12496e-88
NZ_LN831776.1|WP_020430485.1|1020793_1022389_+|response-regulator	gnl|CDD|227095	COG4753, COG4753, Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain [Signal transduction mechanisms].	3.93718e-62
NZ_LN831776.1|WP_081487245.1|1026648_1027419_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	8.70272e-72
NZ_LN831776.1|WP_039789981.1|1027459_1028341_+|family-43-glycosylhydrolase	gnl|CDD|350148	cd18827, GH43_XlnD-like, Glycosyl hydrolase family 43 protein such as Aspergillus niger DMS1957 xylanase D (XlnD); includes mostly xylanases. This glycosyl hydrolase family 43 (GH43) subgroup includes enzymes that have mostly been annotated as xylanases (endo-alpha-L-arabinanase, EC 3.2.1.8). It belongs to the GH43_bXyl-like subgroup of the glycosyl hydrolase clan F (according to carbohydrate-active enzymes database (CAZY)) which includes family 43 (GH43) and 62 (GH62) families. The GH43_bXyl-like subgroup includes enzymes that have been annotated as xylan-digesting beta-xylosidases (EC 3.2.1.37) and xylanases, as well the Bacteroides thetaiotaomicron VPI-5482 alpha-L-arabinofuranosidases (EC 3.2.1.55) (BT3675;BT_3675) and (BT3662;BT_3662). GH43 are inverting enzymes (i.e. they invert the stereochemistry of the anomeric carbon atom of the substrate) that have an aspartate as the catalytic general base, a glutamate as the catalytic general acid and another aspartate that is responsible for pKa modulation and orienting the catalytic acid. Many GH43 enzymes display both alpha-L-arabinofuranosidase and beta-D-xylosidase activity using aryl-glycosides as substrates. A common structural feature of GH43 enzymes is a 5-bladed beta-propeller domain that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	3.96603e-172
NZ_LN831776.1|WP_020430459.1|1033031_1034591_+|AAA-family-ATPase	gnl|CDD|275228	TIGR04435, ABC_transporter, restriction system-associated AAA family ATPase. Members of this family are AAA family ATPases by homology. They occur regularly in a conserved gene neighborhood with the restriction (R), modification (M), and specificity (S) proteins of an apparent type I restriction enzyme system, plus one additional uncharacterized protein. It is not clear whether members of this family contribute to restriction per se, or to another process such as transfer of mobile elements.	3.01892e-14
NZ_LN831776.1|WP_020430491.1|1018249_1019416_+|DUF4317-domain-containing-protein	gnl|CDD|379500	pfam14199, DUF4317, Domain of unknown function (DUF4317). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 225 and 451 amino acids in length. There is a single completely conserved residue P that may be functionally important.	4.50849e-138
NZ_LN831776.1|WP_020430488.1|1019516_1020050_-|NAD(P)H-dependent-oxidoreductase	gnl|CDD|376808	pfam02525, Flavodoxin_2, Flavodoxin-like fold. This family consists of a domain with a flavodoxin-like fold. The family includes bacterial and eukaryotic NAD(P)H dehydrogenase (quinone) EC:1.6.99.2. These enzymes catalyze the NAD(P)H-dependent two-electron reductions of quinones and protect cells against damage by free radicals and reactive oxygen species. This enzyme uses a FAD co-factor. The equation for this reaction is:- NAD(P)H + acceptor <=> NAD(P)(+) + reduced acceptor. This enzyme is also involved in the bioactivation of prodrugs used in chemotherapy. The family also includes acyl carrier protein phosphodiesterase EC:3.1.4.14. This enzyme converts holo-ACP to apo-ACP by hydrolytic cleavage of the phosphopantetheine residue from ACP. This family is related to pfam03358 and pfam00258.	2.02786e-51
NZ_LN831776.1|WP_020430483.1|1022391_1024152_+|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	1.53871e-50
NZ_LN831776.1|WP_020430492.1|1017120_1017855_+|hypothetical-protein	gnl|CDD|180688	PRK06771, PRK06771, hypothetical protein; Provisional.	9.00342e-06
NZ_LN831776.1|WP_020430463.1|1030005_1031037_+|rhamnogalacturonyl-hydrolase	gnl|CDD|226678	COG4225, COG4225, Predicted unsaturated glucuronyl hydrolase involved in regulation of bacterial surface properties, and related proteins [General function prediction only].	1.27325e-96
NZ_LN831776.1|WP_020430481.1|1024278_1025691_+|sugar-ABC-transporter-substrate-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.1485e-76

Protein sequences

>NZ_LN831776.1|WP_039789981.1|1027459_1028341_+|family-43-glycosylhydrolase
MTNPVIPGWYADPEARTYQGRHWIYATRSFTEYTQQMNLDAFSSVDLIHWNKHDSIIEMKDFPWIWRAVWAPTQIEHQGRHYLVFASNDIQKDGEAGGLEIAVADSPEGPYRGYLGKPLIDRFIHGAQPIDAHLFKDDDGAVYLFYGGWGHCNVARMNEDMTGFVAFSDGQTVRSITPPGYVEGPCMIRKDGLYYLMWSMGGWTNGTYRVAYGVSASPLGPFANEGTILERQEPVAEGPGHHGYLHLPDEDEWLIVYHRRIIGDKEPGNRVLCIDRMEFEAGRIKPVIMTDRW
>NZ_LN831776.1|WP_081487245.1|1026648_1027419_+|carbohydrate-ABC-transporter-permease
MFIIPFVWLVRSSLMNLSQIFTMPPEWIPAPFQWSNFQRALTALPFDTFFKNTLIIVVSVLVGTVITSTIGAFGFSRIQWKGRDTVFAILMTSMMLPAAVTMIPSFLGWQALGFYDTLYPLIIPAYFGGGIFNIFLLRQFYLTIPRDFDEAAFVDGASYWQIYTRIIFPLSRSAVIVVALFSFLASWNDFMGPLIYLKSDSLFTLALGLQMFQGSYTAQWDLLMAASATVVLPCVIVFLAGQRYFLEGITLTGLKG
>NZ_LN831776.1|WP_020430472.1|1025704_1026592_+|sugar-ABC-transporter-permease
MRKGMFYGLLFTAPAILGFAVFTLGPMIASLVLSLTDYNVFKEQTSFTGLDHYIRLFSGEDELFYQSLGATFYFVVLRVPAVIILSFAVALLLNLNVKGRAIFRTIIYLPSIVPAVASAMIWMWLLNPDLGLINSLLSRLHLPTSGWLYSEESVIPSVVLTTLWGIGSTVIIFLAGLSGIPRQYYEAIEVDGGGWFHRLRHVTIPMVTPTIFFNTIMTIIGSFQVFNEAYILTQGGPNNKSLFYVFYLWRTGFRDADMGYASALAWILFVIILFFTVIVFRTSKSWVYYEGGERS
>NZ_LN831776.1|WP_020430481.1|1024278_1025691_+|sugar-ABC-transporter-substrate-binding-protein
MLRQRKSLFTVMALVLMLAAVLSACSKSGSESSNTSASSGSSGNSGSKEKITLRMTVWGSPEEVAPYKKAIQRFEDKFPNIKVELQHIAADYDTKLTTMVAGNDVPDVAMMESGTIAFPLAEQGKFYNLQEFLDHDADISPDTLVPNIIYSLEPGNVIGIGPGPESFGLFYNEDIFKEAGIAPPPSNVADAWTWDEFVETAKKLTVDTNGKTAADPDFDPRKIKQYGVNASTWWGVYSNFIYSNGGDFISADGKSFGLNQPEAVEAIQKISDLMNVYHVSPSPVQSKNIPATNVALQTKKVAMTIDGQWASAGLAQSKFNFNVGVMPVLKEPVTTVVCAMFSIFKSTEHPQEAWELMKALVDPEASIDMITAGTWMPSLKDWYTDPALLAKWTENLEARPSGYKEAIVDVILTKGHQTPTGYVKNFNNIMDIVNPALDKVWLGQQSAQEAMDSIAAKVQAQIKGRRDIKE
>NZ_LN831776.1|WP_020430483.1|1022391_1024152_+|sensor-histidine-kinase
MTFRYRLLASYIFLITIPLLVLGTLFYRTSLQIITEQAQKNVYELVKKNNEVMDTKLRIVDQNSMSLFLDKDLFRIFNQLDPANEAGLFEADRQVTAILGKYFSQNQDIYAYQLWTSYFTFGQTLPQGDPTQSDIYEMALQAGGKLVWVPTYDFVSMFHQPYLQSGNLEFRYLFSATRVLDFTYLGNTKLEKMNARAERPVLAISFKSEVLKSLYADSISGSARYMVLDPHDKVVASSEPGAVARTSKEAWLDELKQERSGARRMTLDGEAVIVCFDRSEVTGWMSVVWIPEAGLLSSFVPVIRTSITVLAVVLGIAAFILAFFIAGKITKPIKRLLSAMRSVGEGDFQTRVEVVTNDEFGMLTKRFNRMNDRIHLLVTENYEIKLKEKEAEIQALTMQMHPHFLYNTLNVMNWTAIENGQQELSRMLVCLSNMLHYTSRKTWDAVHLSEEMNWMDNYFYIMSIRFEDKFTVEYAIDPQLYEYDVPRLLFQPFVENAILHGFNQTESGGMIRIRGWIAEGTRFYEVADNGRGMSQETVQAILYQKSSSVGIKNTIDRIQIAYGTLYGVSIVSAPGEGTRVVITLPV
>NZ_LN831776.1|WP_020430485.1|1020793_1022389_+|response-regulator
MRILIVDDEPRHLRGMVNLIHRLRPEDQVAVAKDGLAAMELAKSHRPEAILTDIRMPGMDGLEFLEWLKLEGIKAKVVMVSAYNLFEYAQTAVRHGAYDYLLKPVDVQKIEEVLSRIDVQLNAERKQRREAEALERRLQLSSCAYRNRLILAWLNGSATVPELEELNRYEWLRESGVVVYSELESFREGAQPQDSDQLVSRLEQVWSQWGEALTVPLSGTLEDGRQAAVTLVSLRRLDGEQREKGRALAAALASDWAHTGRLAHGIGPASPSLLAGAPQAYLSARMAYSYNFYEGWKGLVFLDEISSSPLAASPDWGRLYEALKGDDAALVLHVCGEIFTQLAGGGHAVPMLLKEKASLMLLQIRSDNQDILDRKAGQMLADTATRLIRSCSSYKELMARLAKALQEVQLALSLSRQDQGEVVITECLSWIREHTKEEVTLERAADYFHFNPSYFSTLFKSRTGRTFSEHVTAVRMKRAKELLAEDKLRIYEISVECGFQDPKYFCRVFKKYHSMSPKTYKHVLSQRKREA
>NZ_LN831776.1|WP_020430487.1|1020241_1020610_+|helix-turn-helix-transcriptional-regulator
MKQYHLGIEATLEIIGGKWKALIICLLMSGAKRTSELQRNIHGISQKVLIQQLRELEEDGLVRRHVYQQMPPKVEYSLTEYGVTANKIVDIMCTWGKENIKMRQSQGEDIVLLEDESPEDFE
>NZ_LN831776.1|WP_020430488.1|1019516_1020050_-|NAD(P)H-dependent-oxidoreductase
MKTLIILAHPNLEASRVNQRWKEELRQYPNDITVHELYKEYPDGNIDVPREQNLLEGYHHIILQFPLYWYSYPPLLKKWFDEVWTYGWAYGSKGDKLKGKRLGLAISIGDKQENYQPEGSVSFTVDEVIAPFKASAGHVGAVALPYFAVFGASFQASDEDINHSAKEYINYILKHQQ
>NZ_LN831776.1|WP_020430491.1|1018249_1019416_+|DUF4317-domain-containing-protein
MNKKEVAHIRKQFKLDHDLMNIYDILNVYIMKETSEIYHWERLPFGLVDREKQELYMGNFKKLLTGELDHKLFELKFQEEAEEPARVMLHQGLVTGDPEEWQDLMMMLVDKMLVDAKYEKDMVVTFVRGQYYRPTKARNEEAEESGKDEMFAHPFILCSVNSTEQQRKNLMFDYVEREFKYNIIVDPIIKLSSPEQGFFYPSVTDNYSDVNRVLYCTGKSNYPDPQFIEQVLNAERSVTALEERSFFEDIVKELAGEQLDTTTLAQVYEEIQQVIESGEGEEEPPKLDYKDVERVLASSGVENVTAEKVERAFETVIDDKYYEMKASSVIPKYTTKSIKIETKVATISVSPQDLRYVKQVNYQGKRCIMIEVDEEVVIEGFTLNTETL
>NZ_LN831776.1|WP_020430492.1|1017120_1017855_+|hypothetical-protein
MKKNAKVLLFVFLFAATMVLLFGWVLPAVLQAYLHNDYIRGLTLLVVFSIVVLAKRFTWNRNIVYVIAVFTLFSMMIDTAGNPIFNKPLEWIVSPVGELQVMQDVNNYAPGEYAITDHITILKQSGEVLELSTAWLYLYRFVQYLALYSIAGTLLGAVIGMLPQHSLPLIQTAEEFLTEEQEQKAAAEMKRRGEAGNGRQIPPEDIQASVRQLKKDGKLIPAIKLVRQHTDLSLGEAKQYVEKL
>NZ_LN831776.1|WP_020430464.1|1028868_1029810_-|AraC-family-transcriptional-regulator
MPRKKKPVIEYRHYSLPIDFPVLLLSGERWKISDIRSEHLHFHNHLEIGICYSDSGIMEIKGEAVPFTAGDVTFIPRYLPHTTYSSPDTASLWSYLFFSPEDLFQHSFKSAYSSFEPNLWAVTGKNCILNKEQYPKVYTLATSVVEELKQQKPYYQENAYGLLLSLYIELLRIHSTNEMLAEQEAEHSLKGDFVISPALEHITKNYMTPITIDSIAGLCHLSTTHFRRKFHEIMGVAPLDFLSRTRIEEACKQLKSTDHSILSISGQVGFHSISSFNRCFSRLMGESPKQWRKGAQAEAQSAKASILEFTGWV
>NZ_LN831776.1|WP_020430463.1|1030005_1031037_+|rhamnogalacturonyl-hydrolase
MLQLKVDREEILSIIDRVTRKTLAMDLTWEWPCGVAYYGVSRAYQTTGNKEYLDRLVQWTDEYIGLGLPDWTVNTCAMGHMLITLYEETGNQKYWDIVMSKVDYIRNDALRFGDKVLQHTVSVSNDFPEQAWADTLFMAAFFLLRAGSKINDQDLIQDALNQYYWHIKYLQDPGSGFWFHGYNHVQQDHMSGLFWGRANAWGAYTMSQVKPLLKDWYLYPQCMDVECSLRDQLAALKLVQTENGLWRTVLDDEESYEEVSASCGIAAAMINNGNPLHTKYVQKALQGILQNISEDGRVLGVSGGTAVMKDREGYRNIPKDWIQGWGQGLALAFLSDMLKQRNE
>NZ_LN831776.1|WP_020430461.1|1031220_1033056_+|hypothetical-protein
MTEETTRLSKEIRNMIDIVYSGTNNALAVADQLTFFWSVFLLAADGPISLKYPYKMRTSYTWGELVDAEDDAYEVIQIKVLPELLKGHPGYLPKRMASGGLKLTVTETQCYSLITIIDSIYKKLDGVPAFRISLLALYDYMLDILFKGSIEGEDEWMSGESVDFIVSLVDSHLRVEGRGDSIHIHDAHCRSGQLLTASYRELPFIDPRKSLISGRSLSPIMTRISTFRFLLSGIHRFSVLNRDPLVYPSRSFSKAARKNIADRMDVNEIVYILPPRSITFDSRELSDPGLIEQSDHAGVELSYLLYGLNSCAPGGWAFAVLPDELLKTEGVSILEKIETIAQIHSIVRLPKESSRMNIGKNSSLVVILKEPLGIRQQLDDIRRYELSGYRKDDIKLFFTEYEQKAGQTSGSNLTGFIEVRKPKQVKAELEEKLLERISKFEGQLSNLKDPLSIEQKLFSWQTDLYDLGSKQGIALAWQHLIHDNRINTVLSKEGEVVYELNQAGEKRDGYVSIELSGILSPQQWQLYIAISLSESPIAIHKARQRLSMEDRSVFTIQQAVETVQMLARMGMVECIYESVNRGAASPADNEWIDLWMRVPEGGRQWKFTASR
>NZ_LN831776.1|WP_020430459.1|1033031_1034591_+|AAA-family-ATPase
MEIHSLSLENYKHFQTFNGAFGQNDEELSKLSIKFLVGNNGSGKTSVLQAIGLIFTRAMNDESPGFVYELVYSIISGHKRVYVLLSNNSQRYPLTERLYIQMAESLEGIKNGPVVRERYSEQVNLHPRRIISFASGPNNSFEDVLVNSPLGAINSDIYDELKREGRNSGKLEYLQQLQRRLLYEPNCINLNGENAAFILAAIVLAEPVGVEMEGYRTKKNRLFQMVRNIRAELISFELDEVKCRQLEASPLNKMRYESLLVNFLQRGARRIKVVHSLDGTMPKAIRILTIPAGDILSSNPMEFLTMLVTAQRFGYLLNVNLFYKNEDSEHLLDHNSLSDGEFFWLSRMALIILSQQEYDENTLFLFDEPDVFLNENWTMQFISMLHDFAKMDLPGGESSEPRYNRQEYWIATHSTLILTDAFPDQTFKIESHSGVPGEFQAISLDIPTFGADRGEISALLFMDHERIGDFAKQVIDKALDEQKPYSNGRIQKMLDKVGPGYERFRLEEYLHARKQLRSD
>NZ_LN831776.1|WP_167345579.1|1034657_1035848_+|hypothetical-protein
MKLAGECMVALIKYCNTYGITDGQFDEKSFLKLRSHKMYKHCCLMKHPGAMRHRMKELFSTLPVTAIPFFISCLEEDLRFNLNHHQETYHFPGFLNTVFQGILTVDETKKAIDQLPKIFEKFYSDFFDHKESHTLKTNRDRFKDEYIRLNSSKENICPACLGQMHMGKAQLDHYFPKSLFPALVIHPFNIVPICMECNSSVGKKQDRGKGNRVPAWPEDGEAINEPGCLNGVFLPYIRSGQQKFKSRIDGTPGNRVIKVEPLSTAASDEAERIRRHVDTFNLEKAWTNRIPFHFNVLMQRTLSEFARVYTDRVAIGGTVTKEEVGDFLWNKLVLNTEDTLYEVGYQFEFVSYVISMATTPECFHPFYKELLKRMEIRTRKAMPTVPHIYDSFSTTC
>NZ_LN831776.1|WP_020430456.1|1035892_1039258_+|hypothetical-protein
MIFRKDPLDKKSLLKELDSLGYSDRIKKIAVLGRDHRGSTEYSGLLSSLLEDGAYEGRLALAGAEVTKDANVVLSALRHPMASVRNTAAGLLAKVASDTDIERELPHLSQDCRRKLLRSVSFMNRQELAERLLPVVYARWGAEEAVIVLPACRKDTVSQWLTEIGYALKDWNKLAGRHPDAVAEYFKTTLANTPFREQGYVWWRFSSAFEILCRTKAEVVLECAANHGPMGILHPALKKQLSTLTRTNPDAVYRLLTRKESRSDLISQGIPDGVLKRRSYLSLDQWMELAKLLADRPVHIAKILQHLAPSSRKAVFDAVYEEGKRQERIFPEKLLYVLPHALRDKEAARMLGLREVSDDRDRMLRITACRSIHHSREKLEQAAQVSNADERATALMQLIRSTVLSRQGMHETLVYLDRIKNDQDPVRGAVFKELSDSPASAFTDAHVQDLTLLVDSVMDARDTSYGTRFSVQQLAFAILRHNASHPHGELFKFSLNTIQKLAKQSGQLALPSLEKNVPRGIEGILFDAIYTLAAQANRREDYNLVLSLANSFGKRGYGIIKLQQLLKEATRAKTDSTAIQAARHWLAPHDTRDERVGELLALDKSFITIYEVFQHLHRKRQEWLDPYISGAVIKGRFLSGKTIYPVPAADGFNRWLPRQQQSLSSLLGKIAFDAKRSLSERSRVIRIMGSMPDLGPDQLLELIHDKEVPVAEAALHALSLKEEPEKALPVLLENLDGDRARVAMYSIPRCIRRVNPVLLASMLKELLHRDKLKVTVRKEAIRLLGAYRSSDSIPLLLEEFEKPNAHKDVIIAIGHAARQLLDDERSWTILSAMAASLERDIAVSLLSQRPNDLPLDYRPRYLALIIEIAGHPDTFVGSFAFSSMMQWTNGNEEVIAAATAQAITDLEDSNRWKFAMNTLIETCRDGKVNEAVIGVCQKLANTVISDEWNATATRDLPHRQRLMQLINELIALPKNTRIHLVPLYMGLIDCLAYDETLHQVVMRLYIAAIDWNNVEGSVAYLHRMVDCITNQPQLLSDAYKQITHNLQDSTGYWNPETLLEIVDLLGAERGYEHQYIGLSVLEAAGSALLWSPECAGRLRLYRNHTNIAVRSLALNIWTHKL
>NZ_LN831776.1|WP_020430454.1|1039252_1039696_-|acetyltransferase
MNPIHRITDRNEEVSHQLLYIWETAVRATHLFLTEQNIAALSPLVIQGIRQIPHLLAYTDSDHYLGFIGVQDTKIEMLFVNPAVRGRGIGKQLVTYAIQTLNVLYVDVNEQNPQAIGFYEHLGFRVFDRSERDEQGQPFPILHMKLS
>NZ_LN831776.1|WP_020430453.1|1039769_1040897_+|ROK-family-transcriptional-regulator
MATHRLNSMEVKKMNRNAIYRYLYHREATSIQEIAQALNLSLPTVTQNIKELQERELIVETGLFQSTGGRKAKSMACNSVAGYAIGLDVTRNHVGIVIIDLRGTIIKHVRNHFPFANTEVYFKSVGKLVDDCVEESRIDSSKILGVGIALPAILSDDRQTVNYATVIDFKGGSIRRFAEFIRYPCILSNDANAAGFTELWGEKDIHNVVYLSLNNSVGGSIIVNNQIYTGQNHRGGEFGHMTIMPEGRTCYCGQKGCVDAYCSARILSDSTQGSISEFFRRLREGHEPQKAIWQEYIGYLVITVNNLRMLYDCDVILGGYAGAYMEEYIDTLQGLAAQKNTFERDGTYLRVCKYKLEATAVGAALELVTEFIDSI
>NZ_LN831776.1|WP_020430451.1|1041118_1042159_+|NAD(P)-dependent-alcohol-dehydrogenase
MKNRAFYMTDLKKLEMNEIGMPKAKEGEVIVKLEYVGICGSDVHYLEHGRIGDFVVEGDFILGHECAGAVVELGPGVKNLKVGDRVALEPGVTCGQCEFCKSGKYNLCPDVKFLATPPYHGCLMDYIAFPENMAFKLPDNVSSEEGALVEPLAVGLHAAAQGGIKLGDRVVILGAGCIGLVTLLACKAYGATDIVVVDIIEKRLEAAKRLGATRVINAKQENVRDVISLLTDGQGMDKVIETAGSEHTVKQTPYLVKRGGTIVLVGLAAKDIIDFDFMQIMFKEADIKSVFRYRNLYPAAIGAIADGKIDVKGIVTHEFSFEDTQKAFDYVIDNKQEVVKAVIRMG
>NZ_LN831776.1|WP_020430448.1|1042742_1043381_+|glycoside-hydrolase-family-11-protein
MFKFNKKIMTLVMAVSMSCTALFAATASAATDYWQNWTDGGGTVNAVNGSGGNYSVNWSNTGNFVVGKGWTVGSPDRTINYNAGVWAPSGNGYLTLYGWTRNSLIEYYVVDSWGTYRPTGTYKGTVTSDGGTYDIYTTMRYNAPSIDGIQTFQQFWSVRQTKRPTGSNATITFANHVKAWASKGMNLGSSWSYQVLATEGYQSSGSSNVTVW

Crispr_ID: NZ_LN831776_15

• CRISPR_ID: NZ_LN831776_15
• CRISPR_location: 1250088-1250161
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_15

Consensus_repeat	Method
AATTAGTTGCCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_15

>15.1|1250111|28|NZ_LN831776|CRISPRCasFinder
CACCGACGGAGAACAGGGGAATTGAGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_15

CRISPR arrays

The CRISPR arrays of NZ_LN831776_15

>merge|NZ_LN831776|15|1250088-1250161|CRISPRCasFinder
AATTAGTTGCCCTTTTTCCACTTCACCGACGGAGAACAGGGGAATTGAGCAAATTAGTTGCCCTTTTTCCACTT

>NZ_LN831776|15|15|1250088-1250161|CRISPRCasFinder
AATTAGTTGCCCTTTTTCCACTT	CACCGACGGAGAACAGGGGAATTGAGCA
AATTAGTTGCCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_039788164.1|1242597_1243314_-|FAD-dependent-thymidylate-synthase	unknown	unknown	gnl|CDD|376804
NZ_LN831776.1|WP_020427105.1|1258351_1260142_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020428405.1|1246735_1247326_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_LN831776.1|WP_020427107.1|1261114_1261267_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426975.1|1252271_1253882_-|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_020426976.1|1253862_1255698_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_020428399.1|1241116_1242451_+|GntP-family-permease	unknown	unknown	gnl|CDD|225330
NZ_LN831776.1|WP_020428403.1|1244772_1245267_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379326
NZ_LN831776.1|WP_046501348.1|1243980_1244730_+|WecB/TagA/CpsF-family-glycosyltransferase	unknown	unknown	gnl|CDD|377136
NZ_LN831776.1|WP_020427106.1|1260198_1261128_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_039786613.1|1261610_1263389_+|VWA-domain-containing-protein	unknown	unknown	gnl|CDD|365868
NZ_LN831776.1|WP_020428406.1|1247381_1248281_-|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|236841
NZ_LN831776.1|WP_020428407.1|1248567_1249710_+|3-dehydroquinate-synthase	unknown	unknown	gnl|CDD|341474
NZ_LN831776.1|WP_020428398.1|1240286_1241063_+|3-hydroxybutyrate-dehydrogenase	unknown	unknown	gnl|CDD|237100
NZ_LN831776.1|WP_167345584.1|1243480_1243984_+|NUDIX-domain-containing-protein	unknown	unknown	gnl|CDD|239519
NZ_LN831776.1|WP_020426978.1|1256808_1257681_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_046501352.1|1245356_1246559_-|MFS-transporter	unknown	unknown	gnl|CDD|340882
NZ_LN831776.1|WP_020427109.1|1263401_1266791_+|hypothetical-protein	unknown	unknown	gnl|CDD|372732
NZ_LN831776.1|WP_046501356.1|1250485_1252168_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270298
NZ_LN831776.1|WP_020426977.1|1255842_1256793_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_039788164.1|1242597_1243314_-|FAD-dependent-thymidylate-synthase	gnl|CDD|376804	pfam02511, Thy1, Thymidylate synthase complementing protein. Thymidylate synthase complementing protein (Thy1) complements the thymidine growth requirement of the organisms in which it is found, but shows no homology to thymidylate synthase. The bacterial members of this family at least are flavin-dependent thymidylate synthases.	3.48363e-42
NZ_LN831776.1|WP_020428405.1|1246735_1247326_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.05642e-11
NZ_LN831776.1|WP_020426975.1|1252271_1253882_-|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.97173e-49
NZ_LN831776.1|WP_020426976.1|1253862_1255698_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	7.55522e-44
NZ_LN831776.1|WP_020428399.1|1241116_1242451_+|GntP-family-permease	gnl|CDD|225330	COG2610, GntT, H+/gluconate symporter and related permeases [Carbohydrate transport and metabolism / Amino acid transport and metabolism].	2.39199e-57
NZ_LN831776.1|WP_020428403.1|1244772_1245267_+|GNAT-family-N-acetyltransferase	gnl|CDD|379326	pfam13673, Acetyltransf_10, Acetyltransferase (GNAT) domain. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	1.49457e-11
NZ_LN831776.1|WP_046501348.1|1243980_1244730_+|WecB/TagA/CpsF-family-glycosyltransferase	gnl|CDD|377136	pfam03808, Glyco_tran_WecB, Glycosyl transferase WecB/TagA/CpsF family.	2.56115e-71
NZ_LN831776.1|WP_039786613.1|1261610_1263389_+|VWA-domain-containing-protein	gnl|CDD|365868	pfam00092, VWA, von Willebrand factor type A domain.	7.63834e-17
NZ_LN831776.1|WP_020428406.1|1247381_1248281_-|methyltransferase-domain-containing-protein	gnl|CDD|236841	PRK11088, rrmA, 23S rRNA methyltransferase A; Provisional.	1.66232e-38
NZ_LN831776.1|WP_020428407.1|1248567_1249710_+|3-dehydroquinate-synthase	gnl|CDD|341474	cd08195, DHQS, Dehydroquinate synthase (DHQS) catalyzes the conversion of DAHP to DHQ in shikimate pathway for aromatic compounds synthesis. Dehydroquinate synthase (DHQS) catalyzes the conversion of 3-deoxy-D-arabino-heptulosonate-7-phosphate (DAHP) to dehydroquinate (DHQ) in the second step of the shikimate pathway. This pathway, which involves seven sequential enzymatic steps in the conversion of erythrose 4-phosphate and phosphoenolpyruvate into chorismate for subsequent synthesis of aromatic compounds, is found in bacteria, microbial eukaryotes, and plants, but not in mammals. Therefore, enzymes of this pathway are attractive targets for the development of non-toxic antimicrobial compounds, herbicides and anti-parasitic agents. The activity of DHQS requires nicotinamide adenine dinucleotide (NAD) as cofactor. A single active site in DHQS catalyzes five sequential reactions involving alcohol oxidation, phosphate elimination, carbonyl reduction, ring opening, and intramolecular aldol condensation. The binding of substrates and ligands induces domain conformational changes. In some fungi and protozoa, this domain is fused with the other four domains in shikimate pathway and forms a penta-domain AROM protein, which catalyzes steps 2-6 in the shikimate pathway.	6.33322e-150
NZ_LN831776.1|WP_020428398.1|1240286_1241063_+|3-hydroxybutyrate-dehydrogenase	gnl|CDD|237100	PRK12429, PRK12429, 3-hydroxybutyrate dehydrogenase; Provisional.	1.79328e-153
NZ_LN831776.1|WP_167345584.1|1243480_1243984_+|NUDIX-domain-containing-protein	gnl|CDD|239519	cd03427, MTH1, MutT homolog-1 (MTH1) is a member of the Nudix hydrolase superfamily. MTH1, the mammalian counterpart of MutT, hydrolyzes oxidized purine nucleoside triphosphates, such as 8-oxo-dGTP and 2-hydroxy-ATP, to monophosphates, thereby preventing the incorporation of such oxygen radicals during replication. This is an important step in the repair mechanism in genomic and mitochondrial DNA. Like other members of the Nudix family, it requires a divalent cation, such as Mg2+ or Mn2+, for activity, and contain the Nudix motif, a highly conserved 23-residue block (GX5EX7REUXEEXGU, where U = I, L or V), that functions as a metal binding and catalytic site. MTH1 is predominantly localized in the cytoplasm and mitochondria. Structurally, this enzyme adopts a similar fold to MutT despite low sequence similarity outside the conserved nudix motif. The most distinctive structural difference between MutT and MTH1 is the presence of a beta-hairpin, which is absent in MutT. This results in a much deeper and narrower substrate binding pocket. Mechanistically, MTH1 contains dual specificity for nucleotides that contain 2-OH-adenine bases and those that contain 8-oxo-guanine bases.	1.73717e-12
NZ_LN831776.1|WP_020426978.1|1256808_1257681_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.00872e-58
NZ_LN831776.1|WP_046501352.1|1245356_1246559_-|MFS-transporter	gnl|CDD|340882	cd17324, MFS_NepI_like, Purine ribonucleoside efflux pump NepI and similar transporters of the Major Facilitator Superfamily. This family is composed of purine efflux pumps such as Escherichia coli NepI and Bacillus subtilis PbuE, sugar efflux transporters such as Corynebacterium glutamicum arabinose efflux permease, multidrug resistance (MDR) transporters such as Streptomyces lividans chloramphenicol resistance protein (CmlR), and similar proteins. NepI and PbuE are involved in the efflux of purine ribonucleosides such as guanosine, adenosine and inosine, as well as purine bases like guanine, adenine, and hypoxanthine, and purine base analogs. They play a role in the maintenance of cellular purine base pools, as well as in protecting the cells and conferring resistance against toxic purine base analogs such as 6-mercaptopurine. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. The NepI-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	4.44108e-61
NZ_LN831776.1|WP_020427109.1|1263401_1266791_+|hypothetical-protein	gnl|CDD|372732	pfam13809, Tubulin_2, Tubulin like. Many of the residues conserved in Tubulin, pfam00091, are also highly conserved in this family.	3.25123e-83
NZ_LN831776.1|WP_046501356.1|1250485_1252168_-|extracellular-solute-binding-protein	gnl|CDD|270298	cd13580, PBP2_AlgQ_like_1, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	3.55934e-102
NZ_LN831776.1|WP_020426977.1|1255842_1256793_+|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	2.11217e-118

Protein sequences

>NZ_LN831776.1|WP_020428407.1|1248567_1249710_+|3-dehydroquinate-synthase
MSRTFQVMLKKVVDDSYAIEIGEQLFDSLIADLQQGLVPNVSKYAIITDSTVEPLYGRPLLERLRQNGFAAELFSFPAGEASKTRETKALLEDQLLSRAYGRDSCIIAVGGGAVTDLAGFLAGTFGRGVPSLNYATTLLAAADASVGGKTGVNTPVATNLIGLFHQPRKVYIDLAAWRTLPAREFRSGLAETIRHACLGDADFFSYLEENMGKVISDRGQLVLDAGVCEHIALANCRIKYEVVEQDERESNLRQILNLGHTAGRALEALSGYTLLHGEAVAIGLVVQAKLGVKRGYMTEDQAERLIALLKKAGLPTEMPASIPNRQLVDKMYTDKKVRSGRIRFVFQDGIGAMKRFADGSYSIPVEEADILAALEEMPRV
>NZ_LN831776.1|WP_020428406.1|1247381_1248281_-|methyltransferase-domain-containing-protein
MSTTTKKMILAGLMAANPRLFCCPLCASPMSLTEYKSLICSNHHCFDLARNGYINLLSRPAGGKYGKELFASRKAIVNGGFFEPVDTYISGLIAGRKLAGNGPHRILDAGCGEGSHLAAIQELAAAGPHQSLLGVGLDISKEGIALAAKNNNASTLWCVGDLAHSPFGSGQFHTILNILSPSNYAEFQRLLTADGRVIKVIPGQNYLQELRELLYGRSSRQQPNADSEIRERFSETFEITEARHFQYKVSLQPPLLQQLVRMTPLSWAAAQNKLQTVLQLNELEISVDLSVLEGRKLPS
>NZ_LN831776.1|WP_020428405.1|1246735_1247326_+|TetR/AcrR-family-transcriptional-regulator
MVRPREFDEEKALHAAMQIFWEKGYEATSLSDLTATMGIQRPSIYSAFGDKKGLFEAALRMYTKSHAASVRASLHKKASVKAAFRAFFEHLVEEEYREEGSNKGCFCINTMVELSPHDAKFEILTREHQMYLAVIFQETLERGIQSGELDSGTDAKGLAHSLVIALIGLTVMMKCRPERNFMDQAVYSMLSSNGLY
>NZ_LN831776.1|WP_046501352.1|1245356_1246559_-|MFS-transporter
MLFRSEQQLIPSISQKTALLFAAASGLSVANIYFAQPLLDAIAAEFGIRHSAVGIIITLTQICYAAGLLLLVPLGDLLNRRRLITGQMLLSVLALLIVGTASSGTMLSIGIAGIGLLAVAAQTLVAFAASLASPAERGRVVGLVTSGIVIGILLARTFAGLLTDVAGWRAVYLASAGMTLLMAAALYKVLPSVETAKKSLSYLNLIHSVFLLFAHEQILRVRAVLAFLIFTAFSILWTPLVLPLSAPPYSLSHTAIGAFGLAGAAGALGAAKAGRLADRGFGQHTTVIALGLLLLSWLPISRAEHSLFILAIGIIVLDLAVQAVHVTNQSLIFKVRPEARSRLTAGYMIFYSLGSATGSIASTRVYGYAGWNGVCLLGTLVSALALVFALCSSRIRKDSR
>NZ_LN831776.1|WP_020428403.1|1244772_1245267_+|GNAT-family-N-acetyltransferase
MIRLCEKKDEENMYRIINDAAKAYQGVIPGDRYHEPYMSRDELVHEIQHGVVFWGFEDNGELCGVMGIQDKGEVSLIRHAYVRTAQRQGGIGSKLLKHLIERTSKPILIGTWEAAEWAISFYIKNGFKLVPAGEKRNLLSKYWNIPERQIETSVVLSNLGRPGR
>NZ_LN831776.1|WP_046501348.1|1243980_1244730_+|WecB/TagA/CpsF-family-glycosyltransferase
MNGTVSILGVRFSKLTLEETVLHLAEQIENKRDKLFHLITANPEITLASQSDELLQRIIQSADMVVPDGIGIVLAARRQGNPIPERVTGYDLLLKLLEQGNERTWSFYFLGTDEETSRQAVEKITHSYPKVRIAGRHHGFFDAAEEPEIIAGIQQSRPDILILAMGAPYSDKWLHKHKDELAGVKLVFGVGGSLDVISGKVKPTPPVWKKLNLEWAHRLLFSPVAKGQKSRWRRQSALPKFVYRTMIRR
>NZ_LN831776.1|WP_167345584.1|1243480_1243984_+|NUDIX-domain-containing-protein
MAVAFIFNEHREVLFLQKKPTSAFLPGMLVPIGGHMESGEISDPKRACLREIQEETGLGEHELAGLELRYIVHRMKDEREIRIQYIFTGEAAAGSKLVESKEGRLLWVDCSTVSSRHVSASTEEAMRHFLETGIHNHKTYIGTMHGMQGQAVMNWAVLEDWESRVNL
>NZ_LN831776.1|WP_039788164.1|1242597_1243314_-|FAD-dependent-thymidylate-synthase
MILHINVLDKGYVRLVNHMGSDLTVVNAARVSYAKQSEALTEKDIRLIQFLAREGHTSPFRHAVIQLEIYAPLMVARQWWKYVVGSAHYEGTGDSLEAWNESSRRYITEEPAFYIPSAGQWRGAPENSKQGSGGLVAWELGEKYTRELMEYTQLGIQKYEAALADGICAEQARLFLAAYGLYVRWYWTASLQSVTHFLNQRLEHDAQQEIQDYAKAILNIVKTLFPVATEELLTRQQT
>NZ_LN831776.1|WP_020428399.1|1241116_1242451_+|GntP-family-permease
MEIIGSIGIILGVIAIILFALKEIHITVAAPLATLIVVLLNQMDIVTFMLGSESGNFMGALGNYIVKFFAIFLLGAVLAKFMEESGATISIADFILKKFGTQNPYRVLVAIFIVAVILTYGGISLFVVMFAVIPLARTLFKKLDIAWNLIQIPVWLGIGTVTMTILPGTPAIQNVIPIQFLGTSLVAAAIPSIAGALGCTAFGLFYMKYCLNKSLKAGETYATYADDVEESRAERELPGFFASILPLVTLIIIAVLGSTFGNEFVRKNVIYVALIVAILLAVVLFNKHIPDKIRTLSIGASGSIAPIFATASAVAFGSVLMAAPGFEFFSNLITSIPGDPLISLTVLTACISAITGSSSGTLGIVMPNFTDFYLNAGIHPELIHRVAAIASNITTLVPQSGVLLTFLALTKLNHKNGFKEAFITVTVGCAIAVVIVIVLGKFML
>NZ_LN831776.1|WP_020428398.1|1240286_1241063_+|3-hydroxybutyrate-dehydrogenase
MEETKVVFVTGAASGIGKQIGETFLKQGSKVVFSDINDEILQEMVNVLKNEGFDCHGIKCDVTKEDEINSAIDETVEKYGRLDVLINNAGLQHVSLIEDFPTHKFEFMLKVMLVAPFIATKRAFPIMKKQGFGRIINMASINGVIGFAGKSAYNSAKHGVIGLTKVTALEAANSGITVNAICPGYVDTPLVRGQFEDLSKTRNIPLENVLEEVLYPLVPQKRLIDVQEIADYAVFLASEQAKGITGQACLIDGGYTAQ
>NZ_LN831776.1|WP_046501356.1|1250485_1252168_-|extracellular-solute-binding-protein
MVKLNKLGSFLMITALVTLTACSGASNENASKGNAASNSSASTSEADAAFAKGKYDPPIEISSVLMPKKYVHGDTKENNVHDRWMLETLGIKHKDTWYPANDDQYRQKLQLAISSGEKLPDFVSVPTNAVLTNQLIDSGQFIPIDELFDKYANKILKDHAAAHPELWYPFMRDGKKYNMPILEYTDNDDTLLWLREDWMEKLKLEAPKTIADLENIMDKFKNQNPDGLAPKDVYPLAISLKNKTNTWMGSLDWLFGAYGTIEEQWNKDANGNLEYGSVNPGAKQALAKLKEWMDKGYIHADSALWDEGKSAESWTKGTAGILPGANWVPDWPAPDLLKNVKGSKYKAYPIPAGPDGLIGTKWQNSGVNASIMINKDAKHPEAIFLYYNYLLDNMANPTAGSPYEYGFAKGYDWDIIDGQPTSDKEKIKDFSNEFPFLTGPARIPDLYMKTLVKLANGEKPVTPYEKQMAEFRKPENWAAAKIVMSQQNIRKQNYFTGAATPTMVSKWNLLRQSEMETFNKIIYGKLPVDAFDEFVTNWKANGGDQITKEVNDWYKSVSAK
>NZ_LN831776.1|WP_020426975.1|1252271_1253882_-|response-regulator
MQMIIVDDEAHWVDNLSMTKPWHTLGIEQVHKAYSASEALQIIETHPIDIVISDIQMPEMTGLELMERIRRRDKKIKCIILSGHSEFEFAKSAIQHSAVDYLLKPPTDSELLGAVQTAIAQLNAEWELISSLERTQYTLRENLPLLRGQLLLSALQGQRMPADEWERKLENYGLPFRNGDCALMLVRLEEEFGQYKNNGQPLIEYAVINMAEEIIGECMEVWGVKEEHGYLVFLLQLKEKAADLGTDGLLEQLSVQLQYKVKQFLKGSLSIVITEWFRFPDQLPEQFRQASAYFRQIVGDEREFVMRVSDLHEPSEQGPLDALYTPPSLINLLESGHWEAAGAKLMDVCAELDEKWPESWEHCMEAGFLITAAFSNLAHRNGHTLAKLLGTDIEELQSGEAFTSINKLRVWSLSVLGKLKEGTSSEIKDIRSLYVKKIQEFTDKNLHLDVSLRVLADHVNLHPTHLSKIYKIETGEGISEYISRLRMDRACHMLKTTGKKVYEISNDIGYMDPAYFIKVFKRQFGVTPQEYRDGKK
>NZ_LN831776.1|WP_020426976.1|1253862_1255698_-|sensor-histidine-kinase
MGFSQAFMFVKERSWSRFSLFAKMNSLIIVLFVPIIIVYTYSNNVTFDVVSKELQESNTKQLTFLSSQIDSRINQMMDFSVVFSKDPNVRKFNGLGIWEDRYDRMQTRFVIQEKMMLQSGLTDVWPSRYAVYSQQNKDVISNYDKPTGYDENYLIQNMSGKWTYSDDGTGSSSSSKAFYWFHSDSIAPQGTLTGSDLVVEASFSSENIQNMLDTYKTGGQGDPFLYHKGETPILNRTADQKLTADLIRYLDKHSPDSSTQHVISLGHKNYLVSSVKSSYLEWYLVDVVPLDRILGPISVSRNLFYVSMLLLFVVGISASILLYQNVQRPIKKLIKGLRRVQRGDYSVRLHSEDHNEFSFLFYRFNDMSHQIQDLIENVFNEKIRAREATLKQLQAQINPHFLYNCLGFIINMAQMKDEEAVVSMAYNLSAYYRYTTRMERDTATLDDEVRLLVNYLDIQKLRNGRIEYHIDIPQEMLSYSIPRLLLQPIVENSVIHGVGKSYSSGEIRISGECSGGCCRVYIDDDGPGLSPEQQEALNRKMREPLQEEMGCGLWNTNQRLIHQFGNHSALHFTESPLGGFRTEIVWEIPAQEEQPLPTNLQGDTSYANDHC
>NZ_LN831776.1|WP_020426977.1|1255842_1256793_+|sugar-ABC-transporter-permease
MEANTIQQVNPGKPLRQSRKKKVKQPWMLHLMVLPAAVMVFIFSYIPMGGILMAFQDYKPKPGLFGSPWVGLKHFEYMWQNDYFLQITWNTLFFAGTKIIMNLIIPFFFALLLNEVRKMALKRTIQTLVYLPHFLSWVTLSGILIDMLAQTGLINQFISSVFGIKPIFFLGDGSWFRFTIIFSDVWKEFGFNMIIFLAALSGISPSLYEAAEVDGAGRWKQTIYITIPALIPIAIVVATLALGNVLNANFDQVFNLYSPLIYQQGDIIDTFVYREGLLSGQFSFATAVNLFKSAISLILIVISYRLAYRFAGYRIF
>NZ_LN831776.1|WP_020426978.1|1256808_1257681_+|carbohydrate-ABC-transporter-permease
MYHKTVSYRVFSVFNNVFLTLISVLCLLPLFHLLMVSLSSTAPANAGLVTFWPIGFTLEAYAKTFDNANFLSSLWVSVQRTVLGTALALVVNTIAAYALSKETHVFRARNIYLWYFVITMLFSGGLIPGYILILKLGLMDSLLALILPGLVGVFNIILLLNFFRTVPKDLEEAAFIDGAGQFRTFYSIYLPVSMPVLATVSLFIMVGHWNAYFDGIIYIKDASKLPLATFMQTIIVQADMTKLDPAAVANLSQRTIRASQIFISALPILLVYPFLQRYFVTGIVVGAVKE
>NZ_LN831776.1|WP_020427105.1|1258351_1260142_-|hypothetical-protein
MTIKQALSLRNIMIILCILMLVLLGQKGIRLHSKIGAVREAGRLYAAGDLVAAENQYRLAQANASFHYKEAEIAARLQELAPITAIRSGLGLLKLKIEDQLITKDFSGFMESYASLLSLKSQYMKSGGPYESYYRQLSADSGVSGQLGTGFQQFKAQFLAELAAGRSGSSNAVNDGDSFKWNLLRIPDVYLGGTDAKKKLLASEFKAYDTARLKALAAAGSFSPMLDYALSLADAYSSHSYTAPWIASQIEKSAKLILSKDIDGDQIAAFSAHAAAYRKYAASAGLASSKVLSLIDSTSAKLLRSAARLVRSGGYAEAIQRYNDLAPLQDTTAEIAAAQLAWNIAEPARLLPGGETPGKYVLTTSVSGKYGARLAVAGTDSSGQLYYADMGENGAVTTRTGEIIPGFEKLIRLAFDDQLSALAGFPVVVAEGSREDQRTSFAAYTIKPDGISLLFSFAGSSYKLQPDDASIRVANADLRDGSEGQTAIYRQTNGVYQFAEIYQEYPLIDASELELHPLETVNLQVDIYIDSTGRPVAAAGGRYLALQGNVGTVTGPALATGQFQYGYDYAGTDAGEEYVPVFIVESLGSMNPIPNP
>NZ_LN831776.1|WP_020427106.1|1260198_1261128_-|hypothetical-protein
MPVNNKKPVTFRPFKTPRYAYDKLRICRRCGRYTALSEDRCGQCGRAALTAVEQHAAALAGRKMHTRLLFILLLTLAAVYFGQSLQQMALCGAGGIVLAGLLFLTQRKVRQNENLYSLNALLGRSIDSIRDGLEINRQEAVSVLRENDVLAYEKLREISILLRGDRVSRQRIALLHGFQLRKDMQLELEQLLLKDFEPLLAEYIGEIAKVRPELIKDRTLRYVKTYEVQILQMDKGAAILTAVAGAAVRLKRYALLYSGMIGRYVAELPKDRFLRLSRMIDASPYEAWNGLDLKVAEVREAKYRWDPDF
>NZ_LN831776.1|WP_020427107.1|1261114_1261267_-|hypothetical-protein
MISYAILGISFLYAVIQILIYASRQRKPLTRDDIDERLLAALNGGDHARQ
>NZ_LN831776.1|WP_039786613.1|1261610_1263389_+|VWA-domain-containing-protein
MRPIVLLLLVLCISAAPFAGGTASAASPAPSHIDAVLLIDVSNSMNKSDKNNIAGEAMKMFIDMLSAQGDKVGIVAYTDKVQREKALLQIGSAADKQDLKDFIDGLDRGAYTDIAVGMEEAVKVLENGSDPGHEPMIVMLADGNNDLNEATGRTQSQSDQELDAAVETAKQKGYPVYTIGLNADGKLNKEILAGLSNKTSGKAFITDSADDLPQILSEIFADHLKLKVVPVQSITANGSYQEVTVNVPNSSVLEANISIMSAKPVTAKLTDPSGKEVAIPSDDVLLSKSSTYSLIKLLSPEQGDWKLQVKGVPKDKIDINLVFNYDLELKLDALQSKTYKKGDTVEISSHLYSNGAKVTLNNLYQDMKAVLLATDTDTGKVQELPMDNTGAVFKGSFEIAESHNYELKVRAEESSFYRESDVLTINAKTGAVATSTSKPAGAGGTEPAQDKSSSKTLYYIIGGIVLVLAAAVVLWLLRQKSNRGFVGQMVVEVLDGNTGEKTYPQYKKLAAFRGKFTLHQLLQLAPELKESEKLVFTPGKNDRLMLRGSEEISVERSGRVVDTARGLELKSGDRISVALQTVDKTILLEYLI
>NZ_LN831776.1|WP_020427109.1|1263401_1266791_+|hypothetical-protein
MKPVVREHIQQLDVSLGGGIVSDKIRVDTIDNPILIIGLGGTGIDALLRLKYQINRRFKLPEDPLSKKKRDKPDNVEFLAFETNEQDRGKKYKGIGLDPQNEFVLLANAEIGGLLQNRSILEPYITDWLSPELSITDGMNGAAGVRQAGRLLLFTKINQVVSAIDKKIKTLSVGTSKKLMVFLLTGLSGGTGSGSFLDIAYIVRGIIERDYGSAGIDRVNTLGYLFTPDVNLSNKSLSEHTREYIRKNGYAALKELDYWMNVDSRGERFRQQYGNILTVNSPLPPFNLCHLISATNTEGKLLENAYDYCMNVTAENITNFMASEEKQSGEEFAIHDYISNIRTNIAQMNKTYPANYEYNIIGASSAVLPIEEMTTYLAFRLFDKMDKMFQQAPGQEDVEKLARKLGIDLDSMIKTFESRVPEPLPGYENSERLNHSNVIKHQVVDMDTELEQNFLARAREEYIKSKKQLPGEITGRFGEELERIFLHPEQGPFYVSRLLYTEKGFCILKLIQSYIEALRESLLRLPRDIETAQDSAQEKLGDARSAFVSKEKKKNAYIEAKINEYWLHADVERTEQMIEFYEDLFELLNEENNRIYGVFTEILSALSTIFEKNGDILINGEEQADHKGNKTYYWNIVNVPDIASTISKVMDQKDGDDLIRDFTREMLKHSGRWVKEQEIDIVRSISEFLSDKFGDLITRSMEEFLVMKYGREEPLDKFVERIIAGRLDEDAVPIFHLSNSSGSLHFPSWGFVSVPVKAPGILKGIRNYQNNALGKSQFTIKESQVKNRIFWLNTRNGVPLFVYTPLRVYEENYERTILDKEGIGRHLVMTDKNNWTYLPSPIPEKSWGDTYVNNRVREYNARVRADFARALENGVIVEKGLDENTSSRFSVILTKPFDVDKMLSGYDLQLGNSRPNLGEVKKAADELKSLRASGLEREGAKDIFGSINKEMGQENLIRSPQLIARVREELAKYDALAAKAAELEGLLHQYLDEDKWIDQFIEALYTDTITKKGALYVYDRDEDEDAWEPFANLMKERSYVEYAVYRHFRGLDEKSRSVLLRKAARRAGEMTAAEDVTPLLYKLEGLYVSFLEARDSLEYERVEHADGDEMYSFYQSLTGKLGSIRRKLK

Crispr_ID: NZ_LN831776_16

• CRISPR_ID: NZ_LN831776_16
• CRISPR_location: 1258205-1258279
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_16

Consensus_repeat	Method
AATTAGTTAACCTTTTTCCACTTA	CRISPRCasFinder

spacers of NZ_LN831776_16

>16.1|1258229|27|NZ_LN831776|CRISPRCasFinder
ACCTGCGGAGAACAGGGTACCCGGGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_16

CRISPR arrays

The CRISPR arrays of NZ_LN831776_16

>merge|NZ_LN831776|16|1258205-1258279|CRISPRCasFinder
AATTAGTTAACCTTTTTCCACTTAACCTGCGGAGAACAGGGTACCCGGGCAAATTAGTTATCCTTTTTCCACTTA

>NZ_LN831776|16|16|1258205-1258279|CRISPRCasFinder
AATTAGTTAACCTTTTTCCACTTA	ACCTGCGGAGAACAGGGTACCCGGGCA
AATTAGTTATCCTTTTTCCACTTA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020426978.1|1256808_1257681_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_020427112.1|1271144_1271780_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427110.1|1266795_1269231_+|hypothetical-protein	unknown	unknown	gnl|CDD|274008
NZ_LN831776.1|WP_020427107.1|1261114_1261267_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426975.1|1252271_1253882_-|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_020426976.1|1253862_1255698_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_046501356.1|1250485_1252168_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270298
NZ_LN831776.1|WP_020428405.1|1246735_1247326_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_LN831776.1|WP_052741416.1|1273711_1276825_+|hypothetical-protein	unknown	unknown	gnl|CDD|236090
NZ_LN831776.1|WP_020427113.1|1272452_1273715_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046501352.1|1245356_1246559_-|MFS-transporter	unknown	unknown	gnl|CDD|340882
NZ_LN831776.1|WP_039786613.1|1261610_1263389_+|VWA-domain-containing-protein	unknown	unknown	gnl|CDD|365868
NZ_LN831776.1|WP_020428406.1|1247381_1248281_-|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|236841
NZ_LN831776.1|WP_020426977.1|1255842_1256793_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_LN831776.1|WP_020428403.1|1244772_1245267_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379326
NZ_LN831776.1|WP_020427105.1|1258351_1260142_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427111.1|1269691_1270969_+|VWA-domain-containing-protein	unknown	unknown	gnl|CDD|238119
NZ_LN831776.1|WP_020427106.1|1260198_1261128_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427109.1|1263401_1266791_+|hypothetical-protein	unknown	unknown	gnl|CDD|372732
NZ_LN831776.1|WP_020428407.1|1248567_1249710_+|3-dehydroquinate-synthase	unknown	unknown	gnl|CDD|341474

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020426978.1|1256808_1257681_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.00872e-58
NZ_LN831776.1|WP_020427110.1|1266795_1269231_+|hypothetical-protein	gnl|CDD|274008	TIGR02168, Chromosome_partition_protein_Smc, chromosome segregation protein SMC, common bacterial type. SMC (structural maintenance of chromosomes) proteins bind DNA and act in organizing and segregating chromosomes for partition. SMC proteins are found in bacteria, archaea, and eukaryotes. This family represents the SMC protein of most bacteria. The smc gene is often associated with scpB (TIGR00281) and scpA genes, where scp stands for segregation and condensation protein. SMC was shown (in Caulobacter crescentus) to be induced early in S phase but present and bound to DNA throughout the cell cycle. [Cellular processes, Cell division, DNA metabolism, Chromosome-associated proteins].	0.0015607
NZ_LN831776.1|WP_020426975.1|1252271_1253882_-|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.97173e-49
NZ_LN831776.1|WP_020426976.1|1253862_1255698_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	7.55522e-44
NZ_LN831776.1|WP_046501356.1|1250485_1252168_-|extracellular-solute-binding-protein	gnl|CDD|270298	cd13580, PBP2_AlgQ_like_1, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	3.55934e-102
NZ_LN831776.1|WP_020428405.1|1246735_1247326_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.05642e-11
NZ_LN831776.1|WP_052741416.1|1273711_1276825_+|hypothetical-protein	gnl|CDD|236090	PRK07764, PRK07764, DNA polymerase III subunits gamma and tau; Validated.	1.276e-07
NZ_LN831776.1|WP_046501352.1|1245356_1246559_-|MFS-transporter	gnl|CDD|340882	cd17324, MFS_NepI_like, Purine ribonucleoside efflux pump NepI and similar transporters of the Major Facilitator Superfamily. This family is composed of purine efflux pumps such as Escherichia coli NepI and Bacillus subtilis PbuE, sugar efflux transporters such as Corynebacterium glutamicum arabinose efflux permease, multidrug resistance (MDR) transporters such as Streptomyces lividans chloramphenicol resistance protein (CmlR), and similar proteins. NepI and PbuE are involved in the efflux of purine ribonucleosides such as guanosine, adenosine and inosine, as well as purine bases like guanine, adenine, and hypoxanthine, and purine base analogs. They play a role in the maintenance of cellular purine base pools, as well as in protecting the cells and conferring resistance against toxic purine base analogs such as 6-mercaptopurine. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. The NepI-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	4.44108e-61
NZ_LN831776.1|WP_039786613.1|1261610_1263389_+|VWA-domain-containing-protein	gnl|CDD|365868	pfam00092, VWA, von Willebrand factor type A domain.	7.63834e-17
NZ_LN831776.1|WP_020428406.1|1247381_1248281_-|methyltransferase-domain-containing-protein	gnl|CDD|236841	PRK11088, rrmA, 23S rRNA methyltransferase A; Provisional.	1.66232e-38
NZ_LN831776.1|WP_020426977.1|1255842_1256793_+|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	2.11217e-118
NZ_LN831776.1|WP_020428403.1|1244772_1245267_+|GNAT-family-N-acetyltransferase	gnl|CDD|379326	pfam13673, Acetyltransf_10, Acetyltransferase (GNAT) domain. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	1.49457e-11
NZ_LN831776.1|WP_020427111.1|1269691_1270969_+|VWA-domain-containing-protein	gnl|CDD|238119	cd00198, vWFA, Von Willebrand factor type A (vWA) domain was originally found in the blood coagulation protein von Willebrand factor (vWF). Typically, the vWA domain is made up of approximately 200 amino acid residues folded into a classic a/b para-rossmann type of fold. The vWA domain, since its discovery, has drawn great interest because of its widespread occurrence and its involvement in a wide variety of important cellular functions. These include basal membrane formation, cell migration, cell differentiation, adhesion, haemostasis, signaling, chromosomal stability, malignant transformation and in immune defenses In integrins these domains form heterodimers while in vWF it forms multimers. There are different interaction surfaces of this domain as seen by the various molecules it complexes with. Ligand binding in most cases is mediated by the presence of a metal ion dependent adhesion site termed as the MIDAS motif that is a characteristic feature of most, if not all A domains.	1.73484e-20
NZ_LN831776.1|WP_020427109.1|1263401_1266791_+|hypothetical-protein	gnl|CDD|372732	pfam13809, Tubulin_2, Tubulin like. Many of the residues conserved in Tubulin, pfam00091, are also highly conserved in this family.	3.25123e-83
NZ_LN831776.1|WP_020428407.1|1248567_1249710_+|3-dehydroquinate-synthase	gnl|CDD|341474	cd08195, DHQS, Dehydroquinate synthase (DHQS) catalyzes the conversion of DAHP to DHQ in shikimate pathway for aromatic compounds synthesis. Dehydroquinate synthase (DHQS) catalyzes the conversion of 3-deoxy-D-arabino-heptulosonate-7-phosphate (DAHP) to dehydroquinate (DHQ) in the second step of the shikimate pathway. This pathway, which involves seven sequential enzymatic steps in the conversion of erythrose 4-phosphate and phosphoenolpyruvate into chorismate for subsequent synthesis of aromatic compounds, is found in bacteria, microbial eukaryotes, and plants, but not in mammals. Therefore, enzymes of this pathway are attractive targets for the development of non-toxic antimicrobial compounds, herbicides and anti-parasitic agents. The activity of DHQS requires nicotinamide adenine dinucleotide (NAD) as cofactor. A single active site in DHQS catalyzes five sequential reactions involving alcohol oxidation, phosphate elimination, carbonyl reduction, ring opening, and intramolecular aldol condensation. The binding of substrates and ligands induces domain conformational changes. In some fungi and protozoa, this domain is fused with the other four domains in shikimate pathway and forms a penta-domain AROM protein, which catalyzes steps 2-6 in the shikimate pathway.	6.33322e-150

Protein sequences

>NZ_LN831776.1|WP_020426978.1|1256808_1257681_+|carbohydrate-ABC-transporter-permease
MYHKTVSYRVFSVFNNVFLTLISVLCLLPLFHLLMVSLSSTAPANAGLVTFWPIGFTLEAYAKTFDNANFLSSLWVSVQRTVLGTALALVVNTIAAYALSKETHVFRARNIYLWYFVITMLFSGGLIPGYILILKLGLMDSLLALILPGLVGVFNIILLLNFFRTVPKDLEEAAFIDGAGQFRTFYSIYLPVSMPVLATVSLFIMVGHWNAYFDGIIYIKDASKLPLATFMQTIIVQADMTKLDPAAVANLSQRTIRASQIFISALPILLVYPFLQRYFVTGIVVGAVKE
>NZ_LN831776.1|WP_020426977.1|1255842_1256793_+|sugar-ABC-transporter-permease
MEANTIQQVNPGKPLRQSRKKKVKQPWMLHLMVLPAAVMVFIFSYIPMGGILMAFQDYKPKPGLFGSPWVGLKHFEYMWQNDYFLQITWNTLFFAGTKIIMNLIIPFFFALLLNEVRKMALKRTIQTLVYLPHFLSWVTLSGILIDMLAQTGLINQFISSVFGIKPIFFLGDGSWFRFTIIFSDVWKEFGFNMIIFLAALSGISPSLYEAAEVDGAGRWKQTIYITIPALIPIAIVVATLALGNVLNANFDQVFNLYSPLIYQQGDIIDTFVYREGLLSGQFSFATAVNLFKSAISLILIVISYRLAYRFAGYRIF
>NZ_LN831776.1|WP_020426976.1|1253862_1255698_-|sensor-histidine-kinase
MGFSQAFMFVKERSWSRFSLFAKMNSLIIVLFVPIIIVYTYSNNVTFDVVSKELQESNTKQLTFLSSQIDSRINQMMDFSVVFSKDPNVRKFNGLGIWEDRYDRMQTRFVIQEKMMLQSGLTDVWPSRYAVYSQQNKDVISNYDKPTGYDENYLIQNMSGKWTYSDDGTGSSSSSKAFYWFHSDSIAPQGTLTGSDLVVEASFSSENIQNMLDTYKTGGQGDPFLYHKGETPILNRTADQKLTADLIRYLDKHSPDSSTQHVISLGHKNYLVSSVKSSYLEWYLVDVVPLDRILGPISVSRNLFYVSMLLLFVVGISASILLYQNVQRPIKKLIKGLRRVQRGDYSVRLHSEDHNEFSFLFYRFNDMSHQIQDLIENVFNEKIRAREATLKQLQAQINPHFLYNCLGFIINMAQMKDEEAVVSMAYNLSAYYRYTTRMERDTATLDDEVRLLVNYLDIQKLRNGRIEYHIDIPQEMLSYSIPRLLLQPIVENSVIHGVGKSYSSGEIRISGECSGGCCRVYIDDDGPGLSPEQQEALNRKMREPLQEEMGCGLWNTNQRLIHQFGNHSALHFTESPLGGFRTEIVWEIPAQEEQPLPTNLQGDTSYANDHC
>NZ_LN831776.1|WP_020426975.1|1252271_1253882_-|response-regulator
MQMIIVDDEAHWVDNLSMTKPWHTLGIEQVHKAYSASEALQIIETHPIDIVISDIQMPEMTGLELMERIRRRDKKIKCIILSGHSEFEFAKSAIQHSAVDYLLKPPTDSELLGAVQTAIAQLNAEWELISSLERTQYTLRENLPLLRGQLLLSALQGQRMPADEWERKLENYGLPFRNGDCALMLVRLEEEFGQYKNNGQPLIEYAVINMAEEIIGECMEVWGVKEEHGYLVFLLQLKEKAADLGTDGLLEQLSVQLQYKVKQFLKGSLSIVITEWFRFPDQLPEQFRQASAYFRQIVGDEREFVMRVSDLHEPSEQGPLDALYTPPSLINLLESGHWEAAGAKLMDVCAELDEKWPESWEHCMEAGFLITAAFSNLAHRNGHTLAKLLGTDIEELQSGEAFTSINKLRVWSLSVLGKLKEGTSSEIKDIRSLYVKKIQEFTDKNLHLDVSLRVLADHVNLHPTHLSKIYKIETGEGISEYISRLRMDRACHMLKTTGKKVYEISNDIGYMDPAYFIKVFKRQFGVTPQEYRDGKK
>NZ_LN831776.1|WP_046501356.1|1250485_1252168_-|extracellular-solute-binding-protein
MVKLNKLGSFLMITALVTLTACSGASNENASKGNAASNSSASTSEADAAFAKGKYDPPIEISSVLMPKKYVHGDTKENNVHDRWMLETLGIKHKDTWYPANDDQYRQKLQLAISSGEKLPDFVSVPTNAVLTNQLIDSGQFIPIDELFDKYANKILKDHAAAHPELWYPFMRDGKKYNMPILEYTDNDDTLLWLREDWMEKLKLEAPKTIADLENIMDKFKNQNPDGLAPKDVYPLAISLKNKTNTWMGSLDWLFGAYGTIEEQWNKDANGNLEYGSVNPGAKQALAKLKEWMDKGYIHADSALWDEGKSAESWTKGTAGILPGANWVPDWPAPDLLKNVKGSKYKAYPIPAGPDGLIGTKWQNSGVNASIMINKDAKHPEAIFLYYNYLLDNMANPTAGSPYEYGFAKGYDWDIIDGQPTSDKEKIKDFSNEFPFLTGPARIPDLYMKTLVKLANGEKPVTPYEKQMAEFRKPENWAAAKIVMSQQNIRKQNYFTGAATPTMVSKWNLLRQSEMETFNKIIYGKLPVDAFDEFVTNWKANGGDQITKEVNDWYKSVSAK
>NZ_LN831776.1|WP_020428407.1|1248567_1249710_+|3-dehydroquinate-synthase
MSRTFQVMLKKVVDDSYAIEIGEQLFDSLIADLQQGLVPNVSKYAIITDSTVEPLYGRPLLERLRQNGFAAELFSFPAGEASKTRETKALLEDQLLSRAYGRDSCIIAVGGGAVTDLAGFLAGTFGRGVPSLNYATTLLAAADASVGGKTGVNTPVATNLIGLFHQPRKVYIDLAAWRTLPAREFRSGLAETIRHACLGDADFFSYLEENMGKVISDRGQLVLDAGVCEHIALANCRIKYEVVEQDERESNLRQILNLGHTAGRALEALSGYTLLHGEAVAIGLVVQAKLGVKRGYMTEDQAERLIALLKKAGLPTEMPASIPNRQLVDKMYTDKKVRSGRIRFVFQDGIGAMKRFADGSYSIPVEEADILAALEEMPRV
>NZ_LN831776.1|WP_020428406.1|1247381_1248281_-|methyltransferase-domain-containing-protein
MSTTTKKMILAGLMAANPRLFCCPLCASPMSLTEYKSLICSNHHCFDLARNGYINLLSRPAGGKYGKELFASRKAIVNGGFFEPVDTYISGLIAGRKLAGNGPHRILDAGCGEGSHLAAIQELAAAGPHQSLLGVGLDISKEGIALAAKNNNASTLWCVGDLAHSPFGSGQFHTILNILSPSNYAEFQRLLTADGRVIKVIPGQNYLQELRELLYGRSSRQQPNADSEIRERFSETFEITEARHFQYKVSLQPPLLQQLVRMTPLSWAAAQNKLQTVLQLNELEISVDLSVLEGRKLPS
>NZ_LN831776.1|WP_020428405.1|1246735_1247326_+|TetR/AcrR-family-transcriptional-regulator
MVRPREFDEEKALHAAMQIFWEKGYEATSLSDLTATMGIQRPSIYSAFGDKKGLFEAALRMYTKSHAASVRASLHKKASVKAAFRAFFEHLVEEEYREEGSNKGCFCINTMVELSPHDAKFEILTREHQMYLAVIFQETLERGIQSGELDSGTDAKGLAHSLVIALIGLTVMMKCRPERNFMDQAVYSMLSSNGLY
>NZ_LN831776.1|WP_046501352.1|1245356_1246559_-|MFS-transporter
MLFRSEQQLIPSISQKTALLFAAASGLSVANIYFAQPLLDAIAAEFGIRHSAVGIIITLTQICYAAGLLLLVPLGDLLNRRRLITGQMLLSVLALLIVGTASSGTMLSIGIAGIGLLAVAAQTLVAFAASLASPAERGRVVGLVTSGIVIGILLARTFAGLLTDVAGWRAVYLASAGMTLLMAAALYKVLPSVETAKKSLSYLNLIHSVFLLFAHEQILRVRAVLAFLIFTAFSILWTPLVLPLSAPPYSLSHTAIGAFGLAGAAGALGAAKAGRLADRGFGQHTTVIALGLLLLSWLPISRAEHSLFILAIGIIVLDLAVQAVHVTNQSLIFKVRPEARSRLTAGYMIFYSLGSATGSIASTRVYGYAGWNGVCLLGTLVSALALVFALCSSRIRKDSR
>NZ_LN831776.1|WP_020428403.1|1244772_1245267_+|GNAT-family-N-acetyltransferase
MIRLCEKKDEENMYRIINDAAKAYQGVIPGDRYHEPYMSRDELVHEIQHGVVFWGFEDNGELCGVMGIQDKGEVSLIRHAYVRTAQRQGGIGSKLLKHLIERTSKPILIGTWEAAEWAISFYIKNGFKLVPAGEKRNLLSKYWNIPERQIETSVVLSNLGRPGR
>NZ_LN831776.1|WP_020427105.1|1258351_1260142_-|hypothetical-protein
MTIKQALSLRNIMIILCILMLVLLGQKGIRLHSKIGAVREAGRLYAAGDLVAAENQYRLAQANASFHYKEAEIAARLQELAPITAIRSGLGLLKLKIEDQLITKDFSGFMESYASLLSLKSQYMKSGGPYESYYRQLSADSGVSGQLGTGFQQFKAQFLAELAAGRSGSSNAVNDGDSFKWNLLRIPDVYLGGTDAKKKLLASEFKAYDTARLKALAAAGSFSPMLDYALSLADAYSSHSYTAPWIASQIEKSAKLILSKDIDGDQIAAFSAHAAAYRKYAASAGLASSKVLSLIDSTSAKLLRSAARLVRSGGYAEAIQRYNDLAPLQDTTAEIAAAQLAWNIAEPARLLPGGETPGKYVLTTSVSGKYGARLAVAGTDSSGQLYYADMGENGAVTTRTGEIIPGFEKLIRLAFDDQLSALAGFPVVVAEGSREDQRTSFAAYTIKPDGISLLFSFAGSSYKLQPDDASIRVANADLRDGSEGQTAIYRQTNGVYQFAEIYQEYPLIDASELELHPLETVNLQVDIYIDSTGRPVAAAGGRYLALQGNVGTVTGPALATGQFQYGYDYAGTDAGEEYVPVFIVESLGSMNPIPNP
>NZ_LN831776.1|WP_020427106.1|1260198_1261128_-|hypothetical-protein
MPVNNKKPVTFRPFKTPRYAYDKLRICRRCGRYTALSEDRCGQCGRAALTAVEQHAAALAGRKMHTRLLFILLLTLAAVYFGQSLQQMALCGAGGIVLAGLLFLTQRKVRQNENLYSLNALLGRSIDSIRDGLEINRQEAVSVLRENDVLAYEKLREISILLRGDRVSRQRIALLHGFQLRKDMQLELEQLLLKDFEPLLAEYIGEIAKVRPELIKDRTLRYVKTYEVQILQMDKGAAILTAVAGAAVRLKRYALLYSGMIGRYVAELPKDRFLRLSRMIDASPYEAWNGLDLKVAEVREAKYRWDPDF
>NZ_LN831776.1|WP_020427107.1|1261114_1261267_-|hypothetical-protein
MISYAILGISFLYAVIQILIYASRQRKPLTRDDIDERLLAALNGGDHARQ
>NZ_LN831776.1|WP_039786613.1|1261610_1263389_+|VWA-domain-containing-protein
MRPIVLLLLVLCISAAPFAGGTASAASPAPSHIDAVLLIDVSNSMNKSDKNNIAGEAMKMFIDMLSAQGDKVGIVAYTDKVQREKALLQIGSAADKQDLKDFIDGLDRGAYTDIAVGMEEAVKVLENGSDPGHEPMIVMLADGNNDLNEATGRTQSQSDQELDAAVETAKQKGYPVYTIGLNADGKLNKEILAGLSNKTSGKAFITDSADDLPQILSEIFADHLKLKVVPVQSITANGSYQEVTVNVPNSSVLEANISIMSAKPVTAKLTDPSGKEVAIPSDDVLLSKSSTYSLIKLLSPEQGDWKLQVKGVPKDKIDINLVFNYDLELKLDALQSKTYKKGDTVEISSHLYSNGAKVTLNNLYQDMKAVLLATDTDTGKVQELPMDNTGAVFKGSFEIAESHNYELKVRAEESSFYRESDVLTINAKTGAVATSTSKPAGAGGTEPAQDKSSSKTLYYIIGGIVLVLAAAVVLWLLRQKSNRGFVGQMVVEVLDGNTGEKTYPQYKKLAAFRGKFTLHQLLQLAPELKESEKLVFTPGKNDRLMLRGSEEISVERSGRVVDTARGLELKSGDRISVALQTVDKTILLEYLI
>NZ_LN831776.1|WP_020427109.1|1263401_1266791_+|hypothetical-protein
MKPVVREHIQQLDVSLGGGIVSDKIRVDTIDNPILIIGLGGTGIDALLRLKYQINRRFKLPEDPLSKKKRDKPDNVEFLAFETNEQDRGKKYKGIGLDPQNEFVLLANAEIGGLLQNRSILEPYITDWLSPELSITDGMNGAAGVRQAGRLLLFTKINQVVSAIDKKIKTLSVGTSKKLMVFLLTGLSGGTGSGSFLDIAYIVRGIIERDYGSAGIDRVNTLGYLFTPDVNLSNKSLSEHTREYIRKNGYAALKELDYWMNVDSRGERFRQQYGNILTVNSPLPPFNLCHLISATNTEGKLLENAYDYCMNVTAENITNFMASEEKQSGEEFAIHDYISNIRTNIAQMNKTYPANYEYNIIGASSAVLPIEEMTTYLAFRLFDKMDKMFQQAPGQEDVEKLARKLGIDLDSMIKTFESRVPEPLPGYENSERLNHSNVIKHQVVDMDTELEQNFLARAREEYIKSKKQLPGEITGRFGEELERIFLHPEQGPFYVSRLLYTEKGFCILKLIQSYIEALRESLLRLPRDIETAQDSAQEKLGDARSAFVSKEKKKNAYIEAKINEYWLHADVERTEQMIEFYEDLFELLNEENNRIYGVFTEILSALSTIFEKNGDILINGEEQADHKGNKTYYWNIVNVPDIASTISKVMDQKDGDDLIRDFTREMLKHSGRWVKEQEIDIVRSISEFLSDKFGDLITRSMEEFLVMKYGREEPLDKFVERIIAGRLDEDAVPIFHLSNSSGSLHFPSWGFVSVPVKAPGILKGIRNYQNNALGKSQFTIKESQVKNRIFWLNTRNGVPLFVYTPLRVYEENYERTILDKEGIGRHLVMTDKNNWTYLPSPIPEKSWGDTYVNNRVREYNARVRADFARALENGVIVEKGLDENTSSRFSVILTKPFDVDKMLSGYDLQLGNSRPNLGEVKKAADELKSLRASGLEREGAKDIFGSINKEMGQENLIRSPQLIARVREELAKYDALAAKAAELEGLLHQYLDEDKWIDQFIEALYTDTITKKGALYVYDRDEDEDAWEPFANLMKERSYVEYAVYRHFRGLDEKSRSVLLRKAARRAGEMTAAEDVTPLLYKLEGLYVSFLEARDSLEYERVEHADGDEMYSFYQSLTGKLGSIRRKLK
>NZ_LN831776.1|WP_020427110.1|1266795_1269231_+|hypothetical-protein
MIKAQALTYAEQYAAQEEAQRSKGDGRSSIHYPALFLFLGDKVASAIGPVLDGCERKWDNAGGIMALHAASAGSEQAGDGSQPQPEYAGSRNRAQAEGSRRERVLGMALPETAGRDPRTVRQDLYREFHEDSRFLSGMNRSLRRLSNSIADYGRLYSSFDVIHLSIITRVDDPLNVLLPEVALLARAVLSQSFKSVQTDLYVLINEREQGDNFGYSSSVGLAFLRELDGMQQSDYTLSAPLLVTEDGLSIPVAHGPSALFDLVYLLSDKNERGMMSPHGMDDNYEIIAHISLLKNRVRPATDTATGHGGYNNMTFKSGIRGSSGRQGYASAGFSAVRRPNRQIALAVLYHAFHYLAAKLQEGGALSLRERQALLGLSTDSLRERAAALLPDEAGLEEMTGLMSHGRPSYSELKPLSLREAETLLFGDGGQAYFRSNFAEVSARRVADTDPAREWAAVLAAQEKAVPPLTFYQLAEWTAEQPGGGSVLHALRQHMAGLRAAIASAQEELEQLYAESVERQPFQRVPLLDKRTVRNFIHYLFAQVYSRKYELLRMESELALCLRYDAALEQLHAESKAKVQTMEALEEELHSLALASIGRTSETVDQNIMEYYRNVAEEVMRDIEARRGPGIFFSDRFLGSVSELLRQGGAVVAERLIELCRRELLAAEAFALPFEEELLRRANVAAAYDNREIVSREELFKRLYRSLEDEACINVRLFEYTQEHRHEEKYFFGDSSSEFLRYAFGADETTRIYRLGFVHEQRRSGIEKLNLMGGFHLEDLLYYRNGKVYYETYATSGYRLHGIAEEQLPELR
>NZ_LN831776.1|WP_020427111.1|1269691_1270969_+|VWA-domain-containing-protein
MQRKINLLLLLFSLLGGGAAFVLGELLLDQRPYDLPSIVLVGIYFAIVALGVGLGCLLAEMISPKLNGLSWKQRYLGFSWKMLPLTLVLLFAVGSVMEFVYELNFGGVKPVKDVVMVIDDSGSMMQSDPGNSRYKAAESLVQRMDEDNMVAVVTFSQDATVVQPLIPLSSSANREQVTSVINSLQTTDGGTNISGALTEAMGVINSDNQSGRGAMVILLSDGFSQFDTSKELTEYVNRGIAVNTIGLALDDPSGSALLQDIATTTGGQYYDVTNADLLGDVFQQIYDRLGDRTLLTVRSDYTADSPYYAGVRILALLLVGTALGIGLGIVFDNRHLARSFGVGGAVSGLFAGLILEFGLDGHAFGDAMTRLLALLVLAAIIALFTFVIPFGEGRLSRKRGRSADTAAPSSAGFPSPRRNRGSKGF
>NZ_LN831776.1|WP_020427112.1|1271144_1271780_+|hypothetical-protein
MRYAEVDSSTPVITEVSSRVEDRFCTLRWRWPDGVQAVCIHKAPAEAADSGELPPSGMKLYTREEYKANNGYRDRLDDIGLVAYTVYARLADGTDTLLVRQRDGANRTLVSAGKARIYYSIQQKKSLFGKQKTVHMTITAEVPVSKEVLCYVKKRGGFPASKEDGVLFPFVQDFAAGRNILPPIEIGKEDAVRIFFTDGRKYGIFYELVPE
>NZ_LN831776.1|WP_020427113.1|1272452_1273715_+|hypothetical-protein
MSFFNRFKKKNQPQARPLFYDIVCPYCFTRFEPEDVVFRAMHSREDDENYALGEDDALNKYRERFGLDTVDDMEAILNPADIPEEYHHYTDNVLTGLTDRYGVLTRRRLCPSCHNELPVTAGKVPSNIISIIGASQVGKSVYMTSLIHTLQHTTAGHFDAACMPLNAEISRKFRTLYEEPLFERGDLLASTQKEKMQEPFIFQFVFKDESKPPLTLVFFDVAGEGMVDQDYLGLHGQHIKNSAGILFMVDPLQIRSIREKIRINFGDRPGEWVSQYDEPRDVVLTMFGDFIAYQEKSKTDIPTAVVLAKSDMLHSLKDEDGDYIKSNSNVFNNYVHRKTLNLDEFHNIDGEIRRFIEKVDRPFKDTMDVYFANTGYFAVSALGSNPVNQKVEGVVSPIRVDEPFIWLLHKLNYIEGSDGP
>NZ_LN831776.1|WP_052741416.1|1273711_1276825_+|hypothetical-protein
MNRFSGSMIAQQMYTRERRGVYRATEGFDTVAKSESLDNNFVKKILHPFCLYDAPAELAARGEKNEELYPAALHLFHTETNDTVIGQSRYLAADFTGQRSAFFAHNFVVPPIRSEEILEGYGDWLHADFAGSYAGELGGTLPELSAIPVSQREQKPHPLSILRGLGITEELFKTLLQAVMISVAGKKKLYIALDVPIGELSRRAVELTEVLFRALPYDFRRRLGVITYANEPKSRKYIHLTFVEKGSLRPGDRSIEKDFVFDLAAGRVLGADFGDTQQPFAELAWKTLQEPERGLEDFARFADSLLPGESVERKLSLALYNELAVFYEIEQGNESLYTGNKQAVLGGLLAYLKPEGALEARVRLNDMFLERFDREYDLIRQKGVPVPEIMERFVEYFALKGHNYRVKIVDYFINGMLNAQSAGREDALAAAYGIIESNDELSASFFKRVLAQPVFRRALLEPYMESRLSAAASPADILRFVTHWGRFLPEALQQSFVRDTVKEYLLEKLQQSPNPVGEVAAIHDSVDKAEKERRRGSGMYPEVLLLLEELMTASDRFLLNRVSLEELTQEQLLDISFLRYRDAADWQPPLDSITRRKANALRAAYRWFGEEKPTEEIFAGLSPRELDDVQLLGRRWLKESRSIEPFERLPLAFYHSSERQDGPLDYETLMELVKRKAGDNKETVYRFLAWSQGNPLFSISNKKLWPGYRRAILKYFQSSDREAFKSRDFRKSYAAAAGPALQNVYNEARSQLASPLARWVSRSRFQILISGCILGIVLIGAIIAISLLRPDPADTAKPAGSALPSATGGAGALAPAAVRLGGGDTGSGLVFTFAAAADCSAFKPAEISVVSSGDVTEDYQVTGTTSNCLVASGEAAAGTAAAGPDTGADASAPVGSDSGADAAAGAKGAKASAPAGTDGAAAGAGDGSEDGADAGAVTQGPVGGNAGGATPSPAAGGTAPEAPGASGAVPEAPAYEVTVQLEAGAKLVAGDMVIAGEYKLTLQPASGAAASNPPGAGVDASPSPEPSPTATGDTTTE

Crispr_ID: NZ_LN831776_17

• CRISPR_ID: NZ_LN831776_17
• CRISPR_location: 1269249-1269492
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 4 spacers

Consensus repeat of NZ_LN831776_17

Consensus_repeat	Method
ATTCTGTTGCAGAAAGTGCAGCAGAAT	CRISPRCasFinder

spacers of NZ_LN831776_17

>17.1|1269276|25|NZ_LN831776|CRISPRCasFinder
GGCCGGAAATCCGCAGCCAGTGGGT
>17.2|1269328|25|NZ_LN831776|CRISPRCasFinder
GGCTGGAAATCCGCTGTGAGCGTGC
>17.3|1269380|35|NZ_LN831776|CRISPRCasFinder
TCGAAGGATTCGCTTGAATGTGGCTTTTCTTGCAT
>17.4|1269442|24|NZ_LN831776|CRISPRCasFinder
GGGAGTATAGCCTCTTTTGGAGCC

CRISPR arrays and Neighbor proteins around NZ_LN831776_17

CRISPR arrays

The CRISPR arrays of NZ_LN831776_17

>merge|NZ_LN831776|17|1269249-1269492|CRISPRCasFinder
ATTCTGCTGCAGAAAGTGCAGCAGAATGGCCGGAAATCCGCAGCCAGTGGGTATTCTGTTGCAGAAAGTGCAGCAGAATGGCTGGAAATCCGCTGTGAGCGTGCATTCTGCTGCAGAAAGTGCAGCAGAATTCGAAGGATTCGCTTGAATGTGGCTTTTCTTGCATATTCTATTGCAGGAAATGCAATAGAATGGGAGTATAGCCTCTTTTGGAGCCATTCTGCTGCATTACATACACTAGAAT

>NZ_LN831776|17|17|1269249-1269492|CRISPRCasFinder
ATTCTGCTGCAGAAAGTGCAGCAGAAT	GGCCGGAAATCCGCAGCCAGTGGGT
ATTCTGTTGCAGAAAGTGCAGCAGAAT	GGCTGGAAATCCGCTGTGAGCGTGC
ATTCTGCTGCAGAAAGTGCAGCAGAAT	TCGAAGGATTCGCTTGAATGTGGCTTTTCTTGCAT
ATTCTATTGCAGGAAATGCAATAGAAT	GGGAGTATAGCCTCTTTTGGAGCC
ATTCTGCTGCATTACATACACTAGAAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020426978.1|1256808_1257681_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_020427112.1|1271144_1271780_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427110.1|1266795_1269231_+|hypothetical-protein	unknown	unknown	gnl|CDD|274008
NZ_LN831776.1|WP_046501370.1|1284640_1285579_+|DUF4430-domain-containing-protein	unknown	unknown	gnl|CDD|379618
NZ_LN831776.1|WP_020426975.1|1252271_1253882_-|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_020426976.1|1253862_1255698_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_020433224.1|1285575_1286520_+|energy-coupling-factor-transporter-transmembrane-protein-EcfT	unknown	unknown	gnl|CDD|223692
NZ_LN831776.1|WP_052741416.1|1273711_1276825_+|hypothetical-protein	unknown	unknown	gnl|CDD|236090
NZ_LN831776.1|WP_046501367.1|1283853_1284054_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427113.1|1272452_1273715_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427107.1|1261114_1261267_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_039786613.1|1261610_1263389_+|VWA-domain-containing-protein	unknown	unknown	gnl|CDD|365868
NZ_LN831776.1|WP_167345585.1|1277203_1277659_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427106.1|1260198_1261128_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020433225.1|1286435_1288118_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213192
NZ_LN831776.1|WP_020426977.1|1255842_1256793_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_LN831776.1|WP_052741417.1|1278755_1283372_+|DUF4430-domain-containing-protein	unknown	unknown	gnl|CDD|379618
NZ_LN831776.1|WP_020427105.1|1258351_1260142_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427111.1|1269691_1270969_+|VWA-domain-containing-protein	unknown	unknown	gnl|CDD|238119
NZ_LN831776.1|WP_020427109.1|1263401_1266791_+|hypothetical-protein	unknown	unknown	gnl|CDD|372732

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020426978.1|1256808_1257681_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.00872e-58
NZ_LN831776.1|WP_046501370.1|1284640_1285579_+|DUF4430-domain-containing-protein	gnl|CDD|379618	pfam14478, DUF4430, Domain of unknown function (DUF4430). Although this family has overlaps with SLBB, the majority of its sequences are unique. Several family members, eg UniProtKB:A0RGA8, that do not overlap have an LPXTG-cell wall anchor at their C-terminus, a SSF_Family 10_polysaccharide_lyase or Glycosyltransferase structure associated with them in the middle region, as shown by InterPro, as well as this domain at the N-terminus.	1.03865e-19
NZ_LN831776.1|WP_020427110.1|1266795_1269231_+|hypothetical-protein	gnl|CDD|274008	TIGR02168, Chromosome_partition_protein_Smc, chromosome segregation protein SMC, common bacterial type. SMC (structural maintenance of chromosomes) proteins bind DNA and act in organizing and segregating chromosomes for partition. SMC proteins are found in bacteria, archaea, and eukaryotes. This family represents the SMC protein of most bacteria. The smc gene is often associated with scpB (TIGR00281) and scpA genes, where scp stands for segregation and condensation protein. SMC was shown (in Caulobacter crescentus) to be induced early in S phase but present and bound to DNA throughout the cell cycle. [Cellular processes, Cell division, DNA metabolism, Chromosome-associated proteins].	0.0015607
NZ_LN831776.1|WP_020426975.1|1252271_1253882_-|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.97173e-49
NZ_LN831776.1|WP_020426976.1|1253862_1255698_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	7.55522e-44
NZ_LN831776.1|WP_020433224.1|1285575_1286520_+|energy-coupling-factor-transporter-transmembrane-protein-EcfT	gnl|CDD|223692	COG0619, CbiQ, ABC-type cobalt transport system, permease component CbiQ and related transporters [Inorganic ion transport and metabolism].	2.43318e-11
NZ_LN831776.1|WP_052741416.1|1273711_1276825_+|hypothetical-protein	gnl|CDD|236090	PRK07764, PRK07764, DNA polymerase III subunits gamma and tau; Validated.	1.276e-07
NZ_LN831776.1|WP_039786613.1|1261610_1263389_+|VWA-domain-containing-protein	gnl|CDD|365868	pfam00092, VWA, von Willebrand factor type A domain.	7.63834e-17
NZ_LN831776.1|WP_020433225.1|1286435_1288118_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|213192	cd03225, ABC_cobalt_CbiO_domain1, First domain of the ATP-binding cassette component of cobalt transport system. Domain I of the ABC component of a cobalt transport family found in bacteria, archaea, and eukaryota. The transition metal cobalt is an essential component of many enzymes and must be transported into cells in appropriate amounts when needed. This ABC transport system of the CbiMNQO family is involved in cobalt transport in association with the cobalamin (vitamin B12) biosynthetic pathways. Most of cobalt (Cbi) transport systems possess a separate CbiN component, the cobalt-binding periplasmic protein, and they are encoded by the conserved gene cluster cbiMNQO. Both the CbiM and CbiQ proteins are integral cytoplasmic membrane proteins, and the CbiO protein has the linker peptide and the Walker A and B motifs commonly found in the ATPase components of the ABC-type transport systems.	6.14226e-84
NZ_LN831776.1|WP_020426977.1|1255842_1256793_+|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	2.11217e-118
NZ_LN831776.1|WP_052741417.1|1278755_1283372_+|DUF4430-domain-containing-protein	gnl|CDD|379618	pfam14478, DUF4430, Domain of unknown function (DUF4430). Although this family has overlaps with SLBB, the majority of its sequences are unique. Several family members, eg UniProtKB:A0RGA8, that do not overlap have an LPXTG-cell wall anchor at their C-terminus, a SSF_Family 10_polysaccharide_lyase or Glycosyltransferase structure associated with them in the middle region, as shown by InterPro, as well as this domain at the N-terminus.	2.12575e-14
NZ_LN831776.1|WP_020427111.1|1269691_1270969_+|VWA-domain-containing-protein	gnl|CDD|238119	cd00198, vWFA, Von Willebrand factor type A (vWA) domain was originally found in the blood coagulation protein von Willebrand factor (vWF). Typically, the vWA domain is made up of approximately 200 amino acid residues folded into a classic a/b para-rossmann type of fold. The vWA domain, since its discovery, has drawn great interest because of its widespread occurrence and its involvement in a wide variety of important cellular functions. These include basal membrane formation, cell migration, cell differentiation, adhesion, haemostasis, signaling, chromosomal stability, malignant transformation and in immune defenses In integrins these domains form heterodimers while in vWF it forms multimers. There are different interaction surfaces of this domain as seen by the various molecules it complexes with. Ligand binding in most cases is mediated by the presence of a metal ion dependent adhesion site termed as the MIDAS motif that is a characteristic feature of most, if not all A domains.	1.73484e-20
NZ_LN831776.1|WP_020427109.1|1263401_1266791_+|hypothetical-protein	gnl|CDD|372732	pfam13809, Tubulin_2, Tubulin like. Many of the residues conserved in Tubulin, pfam00091, are also highly conserved in this family.	3.25123e-83

Protein sequences

>NZ_LN831776.1|WP_020427110.1|1266795_1269231_+|hypothetical-protein
MIKAQALTYAEQYAAQEEAQRSKGDGRSSIHYPALFLFLGDKVASAIGPVLDGCERKWDNAGGIMALHAASAGSEQAGDGSQPQPEYAGSRNRAQAEGSRRERVLGMALPETAGRDPRTVRQDLYREFHEDSRFLSGMNRSLRRLSNSIADYGRLYSSFDVIHLSIITRVDDPLNVLLPEVALLARAVLSQSFKSVQTDLYVLINEREQGDNFGYSSSVGLAFLRELDGMQQSDYTLSAPLLVTEDGLSIPVAHGPSALFDLVYLLSDKNERGMMSPHGMDDNYEIIAHISLLKNRVRPATDTATGHGGYNNMTFKSGIRGSSGRQGYASAGFSAVRRPNRQIALAVLYHAFHYLAAKLQEGGALSLRERQALLGLSTDSLRERAAALLPDEAGLEEMTGLMSHGRPSYSELKPLSLREAETLLFGDGGQAYFRSNFAEVSARRVADTDPAREWAAVLAAQEKAVPPLTFYQLAEWTAEQPGGGSVLHALRQHMAGLRAAIASAQEELEQLYAESVERQPFQRVPLLDKRTVRNFIHYLFAQVYSRKYELLRMESELALCLRYDAALEQLHAESKAKVQTMEALEEELHSLALASIGRTSETVDQNIMEYYRNVAEEVMRDIEARRGPGIFFSDRFLGSVSELLRQGGAVVAERLIELCRRELLAAEAFALPFEEELLRRANVAAAYDNREIVSREELFKRLYRSLEDEACINVRLFEYTQEHRHEEKYFFGDSSSEFLRYAFGADETTRIYRLGFVHEQRRSGIEKLNLMGGFHLEDLLYYRNGKVYYETYATSGYRLHGIAEEQLPELR
>NZ_LN831776.1|WP_020427109.1|1263401_1266791_+|hypothetical-protein
MKPVVREHIQQLDVSLGGGIVSDKIRVDTIDNPILIIGLGGTGIDALLRLKYQINRRFKLPEDPLSKKKRDKPDNVEFLAFETNEQDRGKKYKGIGLDPQNEFVLLANAEIGGLLQNRSILEPYITDWLSPELSITDGMNGAAGVRQAGRLLLFTKINQVVSAIDKKIKTLSVGTSKKLMVFLLTGLSGGTGSGSFLDIAYIVRGIIERDYGSAGIDRVNTLGYLFTPDVNLSNKSLSEHTREYIRKNGYAALKELDYWMNVDSRGERFRQQYGNILTVNSPLPPFNLCHLISATNTEGKLLENAYDYCMNVTAENITNFMASEEKQSGEEFAIHDYISNIRTNIAQMNKTYPANYEYNIIGASSAVLPIEEMTTYLAFRLFDKMDKMFQQAPGQEDVEKLARKLGIDLDSMIKTFESRVPEPLPGYENSERLNHSNVIKHQVVDMDTELEQNFLARAREEYIKSKKQLPGEITGRFGEELERIFLHPEQGPFYVSRLLYTEKGFCILKLIQSYIEALRESLLRLPRDIETAQDSAQEKLGDARSAFVSKEKKKNAYIEAKINEYWLHADVERTEQMIEFYEDLFELLNEENNRIYGVFTEILSALSTIFEKNGDILINGEEQADHKGNKTYYWNIVNVPDIASTISKVMDQKDGDDLIRDFTREMLKHSGRWVKEQEIDIVRSISEFLSDKFGDLITRSMEEFLVMKYGREEPLDKFVERIIAGRLDEDAVPIFHLSNSSGSLHFPSWGFVSVPVKAPGILKGIRNYQNNALGKSQFTIKESQVKNRIFWLNTRNGVPLFVYTPLRVYEENYERTILDKEGIGRHLVMTDKNNWTYLPSPIPEKSWGDTYVNNRVREYNARVRADFARALENGVIVEKGLDENTSSRFSVILTKPFDVDKMLSGYDLQLGNSRPNLGEVKKAADELKSLRASGLEREGAKDIFGSINKEMGQENLIRSPQLIARVREELAKYDALAAKAAELEGLLHQYLDEDKWIDQFIEALYTDTITKKGALYVYDRDEDEDAWEPFANLMKERSYVEYAVYRHFRGLDEKSRSVLLRKAARRAGEMTAAEDVTPLLYKLEGLYVSFLEARDSLEYERVEHADGDEMYSFYQSLTGKLGSIRRKLK
>NZ_LN831776.1|WP_039786613.1|1261610_1263389_+|VWA-domain-containing-protein
MRPIVLLLLVLCISAAPFAGGTASAASPAPSHIDAVLLIDVSNSMNKSDKNNIAGEAMKMFIDMLSAQGDKVGIVAYTDKVQREKALLQIGSAADKQDLKDFIDGLDRGAYTDIAVGMEEAVKVLENGSDPGHEPMIVMLADGNNDLNEATGRTQSQSDQELDAAVETAKQKGYPVYTIGLNADGKLNKEILAGLSNKTSGKAFITDSADDLPQILSEIFADHLKLKVVPVQSITANGSYQEVTVNVPNSSVLEANISIMSAKPVTAKLTDPSGKEVAIPSDDVLLSKSSTYSLIKLLSPEQGDWKLQVKGVPKDKIDINLVFNYDLELKLDALQSKTYKKGDTVEISSHLYSNGAKVTLNNLYQDMKAVLLATDTDTGKVQELPMDNTGAVFKGSFEIAESHNYELKVRAEESSFYRESDVLTINAKTGAVATSTSKPAGAGGTEPAQDKSSSKTLYYIIGGIVLVLAAAVVLWLLRQKSNRGFVGQMVVEVLDGNTGEKTYPQYKKLAAFRGKFTLHQLLQLAPELKESEKLVFTPGKNDRLMLRGSEEISVERSGRVVDTARGLELKSGDRISVALQTVDKTILLEYLI
>NZ_LN831776.1|WP_020427107.1|1261114_1261267_-|hypothetical-protein
MISYAILGISFLYAVIQILIYASRQRKPLTRDDIDERLLAALNGGDHARQ
>NZ_LN831776.1|WP_020427106.1|1260198_1261128_-|hypothetical-protein
MPVNNKKPVTFRPFKTPRYAYDKLRICRRCGRYTALSEDRCGQCGRAALTAVEQHAAALAGRKMHTRLLFILLLTLAAVYFGQSLQQMALCGAGGIVLAGLLFLTQRKVRQNENLYSLNALLGRSIDSIRDGLEINRQEAVSVLRENDVLAYEKLREISILLRGDRVSRQRIALLHGFQLRKDMQLELEQLLLKDFEPLLAEYIGEIAKVRPELIKDRTLRYVKTYEVQILQMDKGAAILTAVAGAAVRLKRYALLYSGMIGRYVAELPKDRFLRLSRMIDASPYEAWNGLDLKVAEVREAKYRWDPDF
>NZ_LN831776.1|WP_020427105.1|1258351_1260142_-|hypothetical-protein
MTIKQALSLRNIMIILCILMLVLLGQKGIRLHSKIGAVREAGRLYAAGDLVAAENQYRLAQANASFHYKEAEIAARLQELAPITAIRSGLGLLKLKIEDQLITKDFSGFMESYASLLSLKSQYMKSGGPYESYYRQLSADSGVSGQLGTGFQQFKAQFLAELAAGRSGSSNAVNDGDSFKWNLLRIPDVYLGGTDAKKKLLASEFKAYDTARLKALAAAGSFSPMLDYALSLADAYSSHSYTAPWIASQIEKSAKLILSKDIDGDQIAAFSAHAAAYRKYAASAGLASSKVLSLIDSTSAKLLRSAARLVRSGGYAEAIQRYNDLAPLQDTTAEIAAAQLAWNIAEPARLLPGGETPGKYVLTTSVSGKYGARLAVAGTDSSGQLYYADMGENGAVTTRTGEIIPGFEKLIRLAFDDQLSALAGFPVVVAEGSREDQRTSFAAYTIKPDGISLLFSFAGSSYKLQPDDASIRVANADLRDGSEGQTAIYRQTNGVYQFAEIYQEYPLIDASELELHPLETVNLQVDIYIDSTGRPVAAAGGRYLALQGNVGTVTGPALATGQFQYGYDYAGTDAGEEYVPVFIVESLGSMNPIPNP
>NZ_LN831776.1|WP_020426978.1|1256808_1257681_+|carbohydrate-ABC-transporter-permease
MYHKTVSYRVFSVFNNVFLTLISVLCLLPLFHLLMVSLSSTAPANAGLVTFWPIGFTLEAYAKTFDNANFLSSLWVSVQRTVLGTALALVVNTIAAYALSKETHVFRARNIYLWYFVITMLFSGGLIPGYILILKLGLMDSLLALILPGLVGVFNIILLLNFFRTVPKDLEEAAFIDGAGQFRTFYSIYLPVSMPVLATVSLFIMVGHWNAYFDGIIYIKDASKLPLATFMQTIIVQADMTKLDPAAVANLSQRTIRASQIFISALPILLVYPFLQRYFVTGIVVGAVKE
>NZ_LN831776.1|WP_020426977.1|1255842_1256793_+|sugar-ABC-transporter-permease
MEANTIQQVNPGKPLRQSRKKKVKQPWMLHLMVLPAAVMVFIFSYIPMGGILMAFQDYKPKPGLFGSPWVGLKHFEYMWQNDYFLQITWNTLFFAGTKIIMNLIIPFFFALLLNEVRKMALKRTIQTLVYLPHFLSWVTLSGILIDMLAQTGLINQFISSVFGIKPIFFLGDGSWFRFTIIFSDVWKEFGFNMIIFLAALSGISPSLYEAAEVDGAGRWKQTIYITIPALIPIAIVVATLALGNVLNANFDQVFNLYSPLIYQQGDIIDTFVYREGLLSGQFSFATAVNLFKSAISLILIVISYRLAYRFAGYRIF
>NZ_LN831776.1|WP_020426976.1|1253862_1255698_-|sensor-histidine-kinase
MGFSQAFMFVKERSWSRFSLFAKMNSLIIVLFVPIIIVYTYSNNVTFDVVSKELQESNTKQLTFLSSQIDSRINQMMDFSVVFSKDPNVRKFNGLGIWEDRYDRMQTRFVIQEKMMLQSGLTDVWPSRYAVYSQQNKDVISNYDKPTGYDENYLIQNMSGKWTYSDDGTGSSSSSKAFYWFHSDSIAPQGTLTGSDLVVEASFSSENIQNMLDTYKTGGQGDPFLYHKGETPILNRTADQKLTADLIRYLDKHSPDSSTQHVISLGHKNYLVSSVKSSYLEWYLVDVVPLDRILGPISVSRNLFYVSMLLLFVVGISASILLYQNVQRPIKKLIKGLRRVQRGDYSVRLHSEDHNEFSFLFYRFNDMSHQIQDLIENVFNEKIRAREATLKQLQAQINPHFLYNCLGFIINMAQMKDEEAVVSMAYNLSAYYRYTTRMERDTATLDDEVRLLVNYLDIQKLRNGRIEYHIDIPQEMLSYSIPRLLLQPIVENSVIHGVGKSYSSGEIRISGECSGGCCRVYIDDDGPGLSPEQQEALNRKMREPLQEEMGCGLWNTNQRLIHQFGNHSALHFTESPLGGFRTEIVWEIPAQEEQPLPTNLQGDTSYANDHC
>NZ_LN831776.1|WP_020426975.1|1252271_1253882_-|response-regulator
MQMIIVDDEAHWVDNLSMTKPWHTLGIEQVHKAYSASEALQIIETHPIDIVISDIQMPEMTGLELMERIRRRDKKIKCIILSGHSEFEFAKSAIQHSAVDYLLKPPTDSELLGAVQTAIAQLNAEWELISSLERTQYTLRENLPLLRGQLLLSALQGQRMPADEWERKLENYGLPFRNGDCALMLVRLEEEFGQYKNNGQPLIEYAVINMAEEIIGECMEVWGVKEEHGYLVFLLQLKEKAADLGTDGLLEQLSVQLQYKVKQFLKGSLSIVITEWFRFPDQLPEQFRQASAYFRQIVGDEREFVMRVSDLHEPSEQGPLDALYTPPSLINLLESGHWEAAGAKLMDVCAELDEKWPESWEHCMEAGFLITAAFSNLAHRNGHTLAKLLGTDIEELQSGEAFTSINKLRVWSLSVLGKLKEGTSSEIKDIRSLYVKKIQEFTDKNLHLDVSLRVLADHVNLHPTHLSKIYKIETGEGISEYISRLRMDRACHMLKTTGKKVYEISNDIGYMDPAYFIKVFKRQFGVTPQEYRDGKK
>NZ_LN831776.1|WP_020427111.1|1269691_1270969_+|VWA-domain-containing-protein
MQRKINLLLLLFSLLGGGAAFVLGELLLDQRPYDLPSIVLVGIYFAIVALGVGLGCLLAEMISPKLNGLSWKQRYLGFSWKMLPLTLVLLFAVGSVMEFVYELNFGGVKPVKDVVMVIDDSGSMMQSDPGNSRYKAAESLVQRMDEDNMVAVVTFSQDATVVQPLIPLSSSANREQVTSVINSLQTTDGGTNISGALTEAMGVINSDNQSGRGAMVILLSDGFSQFDTSKELTEYVNRGIAVNTIGLALDDPSGSALLQDIATTTGGQYYDVTNADLLGDVFQQIYDRLGDRTLLTVRSDYTADSPYYAGVRILALLLVGTALGIGLGIVFDNRHLARSFGVGGAVSGLFAGLILEFGLDGHAFGDAMTRLLALLVLAAIIALFTFVIPFGEGRLSRKRGRSADTAAPSSAGFPSPRRNRGSKGF
>NZ_LN831776.1|WP_020427112.1|1271144_1271780_+|hypothetical-protein
MRYAEVDSSTPVITEVSSRVEDRFCTLRWRWPDGVQAVCIHKAPAEAADSGELPPSGMKLYTREEYKANNGYRDRLDDIGLVAYTVYARLADGTDTLLVRQRDGANRTLVSAGKARIYYSIQQKKSLFGKQKTVHMTITAEVPVSKEVLCYVKKRGGFPASKEDGVLFPFVQDFAAGRNILPPIEIGKEDAVRIFFTDGRKYGIFYELVPE
>NZ_LN831776.1|WP_020427113.1|1272452_1273715_+|hypothetical-protein
MSFFNRFKKKNQPQARPLFYDIVCPYCFTRFEPEDVVFRAMHSREDDENYALGEDDALNKYRERFGLDTVDDMEAILNPADIPEEYHHYTDNVLTGLTDRYGVLTRRRLCPSCHNELPVTAGKVPSNIISIIGASQVGKSVYMTSLIHTLQHTTAGHFDAACMPLNAEISRKFRTLYEEPLFERGDLLASTQKEKMQEPFIFQFVFKDESKPPLTLVFFDVAGEGMVDQDYLGLHGQHIKNSAGILFMVDPLQIRSIREKIRINFGDRPGEWVSQYDEPRDVVLTMFGDFIAYQEKSKTDIPTAVVLAKSDMLHSLKDEDGDYIKSNSNVFNNYVHRKTLNLDEFHNIDGEIRRFIEKVDRPFKDTMDVYFANTGYFAVSALGSNPVNQKVEGVVSPIRVDEPFIWLLHKLNYIEGSDGP
>NZ_LN831776.1|WP_052741416.1|1273711_1276825_+|hypothetical-protein
MNRFSGSMIAQQMYTRERRGVYRATEGFDTVAKSESLDNNFVKKILHPFCLYDAPAELAARGEKNEELYPAALHLFHTETNDTVIGQSRYLAADFTGQRSAFFAHNFVVPPIRSEEILEGYGDWLHADFAGSYAGELGGTLPELSAIPVSQREQKPHPLSILRGLGITEELFKTLLQAVMISVAGKKKLYIALDVPIGELSRRAVELTEVLFRALPYDFRRRLGVITYANEPKSRKYIHLTFVEKGSLRPGDRSIEKDFVFDLAAGRVLGADFGDTQQPFAELAWKTLQEPERGLEDFARFADSLLPGESVERKLSLALYNELAVFYEIEQGNESLYTGNKQAVLGGLLAYLKPEGALEARVRLNDMFLERFDREYDLIRQKGVPVPEIMERFVEYFALKGHNYRVKIVDYFINGMLNAQSAGREDALAAAYGIIESNDELSASFFKRVLAQPVFRRALLEPYMESRLSAAASPADILRFVTHWGRFLPEALQQSFVRDTVKEYLLEKLQQSPNPVGEVAAIHDSVDKAEKERRRGSGMYPEVLLLLEELMTASDRFLLNRVSLEELTQEQLLDISFLRYRDAADWQPPLDSITRRKANALRAAYRWFGEEKPTEEIFAGLSPRELDDVQLLGRRWLKESRSIEPFERLPLAFYHSSERQDGPLDYETLMELVKRKAGDNKETVYRFLAWSQGNPLFSISNKKLWPGYRRAILKYFQSSDREAFKSRDFRKSYAAAAGPALQNVYNEARSQLASPLARWVSRSRFQILISGCILGIVLIGAIIAISLLRPDPADTAKPAGSALPSATGGAGALAPAAVRLGGGDTGSGLVFTFAAAADCSAFKPAEISVVSSGDVTEDYQVTGTTSNCLVASGEAAAGTAAAGPDTGADASAPVGSDSGADAAAGAKGAKASAPAGTDGAAAGAGDGSEDGADAGAVTQGPVGGNAGGATPSPAAGGTAPEAPGASGAVPEAPAYEVTVQLEAGAKLVAGDMVIAGEYKLTLQPASGAAASNPPGAGVDASPSPEPSPTATGDTTTE
>NZ_LN831776.1|WP_167345585.1|1277203_1277659_+|hypothetical-protein
MLETTAEMPLLGAPSLEMLETTAEMPLLGAPSLEMLETTAEMPLLCTPSLEMLETTAEMPLLGAPSLEMLETTAEKPLLGALSLELLETTAEMPLLGAPSLEMLETTVEMPLLCTPSLEMLETTAEMPLLCAPRPKLVDTTAEIPLLPPLL
>NZ_LN831776.1|WP_052741417.1|1278755_1283372_+|DUF4430-domain-containing-protein
MKTFYSAKSFVLGLVLLLVISVTGTAVVPAGQAFAAAEATVNTGTDSVTDAVYAADTFAEGKAGASLAAADNGGQVTVSQATYSAAEYILSGGVTSEWQAIGLAQAGYRVPDSYVQSLAKKVQTAGGSFPNVTDYARIVLAVRAVGGDPANFAGSGSEAGFNLLERIYNSDNISGQPLNAPVYALLALDSGSYTIPGDAKWNQTSLLSEILSKQNSDGGFALFTGASDPDMTAIVLTALAAHKNDPAVATAGQKAVAWLAAKQDSSGGYGDSSESAAQAIIGLSSFGVDPASGEFTKNETGLLNRLLSFRLASGAFAHNQGGSANALATEQGLQALVAYNLFSGGTNGKLYDFSKPVAQNPLVYVPLTIEGPEQTLGQGSAYAGNVLEALEKVAAANSLPITNPSGAYVTGIGSIYAGATGGYDGWMYAVSRGGEWASVDVGMKDFKLKESDRVLVYYAGSATQLVDKVALSNAQPREGEAFTVTVTQKTWVWDGSASNPVTSRAAGVQVTIGGKTATTDKDGKAEFPEGFAAEDYTLAVTGYVAEKAPKIAKYTQTLKVAPLNVKATVSVEGPQGPIAEGTLEASDALDALKKLAASGNIPLDITESSFGSYVSGINGIQSGTYDGYWSFVVSRGGEWIYPSVGMGAFVLQPSDHVLVYYGGGATQVVNSVTLSAAQPKPGEAFTVNVAQKQWVWNDKTYTSDPVVTPAAGVQVTIGSTTVTTDQKGAATIDNGLPAGAYKIAVTGYVADSTPKIVRYTQPLTISDPVVVPQPASATISVIGDSAKGTILSSTTVALNAGETAYSLLIRQLGSRVTATTSGGSMYVVAIDGLKEFDRGPKSGWKYSVNGSDPGFSAGDYKLNNGDVLVWYYTTDYDIPSAGTGGLSGNTGSTGGAGSVGIAVDNTLPLNQVGQTTAVTNSGAPMTASEAAALGQKLTANTAAFEQEVTSGAGAALKDSGGEVQLLIPAGAVSGTVKISMKESSSSRGELVSGLYTFGPDGTKFVKPVDLSITVPVKSGNPANLALAWLDPATGRWIPVPSVLDAKTGIITGKISHFTDYAVVDRSKWEPQPEKLKSDIAATAKGITAAEELSDWQAVGLARSGHAVPAAYLEGVKEQLSASKGQLRKVTDYERLVLGVAAAGADPQNFGGYNLIEKIYNNDNMTSQGSNGLIFALIALDSGSYTVPSGAKWTKERLVQALLEVQSKDGGFPLTSGGAADPDITAMAVTALSAHASQTTVAAAVDKAIAWLSQQQQEDGGFKQANVENSESTAQVIIALAAAGIGPNDSRFVKTKGGLLSHLASFRQADGGYAHTQGQPANSVATEQALLALTAYNRYLTGEANLFSISPTGVNGGVVFTDENLISPWALEAVHQAYGKKLMEGISGNSLVFAPKQKITRAEFAALLLRLTHNEPSVANSAPVFSDVKTGTWYYGVVRKAKELGIADGITDTTFNPNGVISRQDMAVMISRALKLENTASAAAPQAAKFTDEGRISSYAVSAVRTVTELGYMTGFGGTFDPSSAVTREMAAVVAVRLP
>NZ_LN831776.1|WP_046501367.1|1283853_1284054_+|hypothetical-protein
MISKSAEKWNLLHSVQQIQAKKALLTPNQEISARNAAECDLPQTAQFSIVVQSAIKQKVYELNWRT
>NZ_LN831776.1|WP_046501370.1|1284640_1285579_+|DUF4430-domain-containing-protein
MSKSIQQWLFTPLLLLSAAVLLAGCAAGADTAGGAQSPAAGTAAVQSPQPKTPASPLPGDAATPVPSAAADGTAPPSGAEPAAGTQKGAAVSAPPASSGAAAKPAPSAAAVTEPASVTASAAPATAKASAGPAKPAAGAKPTASTKPAAGAKPTASTKPTAGAQPAAGTKPAATAKPAATAQAPAAASAAPAKPAGAVNTVTLSIVGDKEHGTIFAAAAVDIKSGESALELLKRITRSNKIQMEYQGAKSFAYVEGIDNLYEFDQGPESGWIYKVNGEVPGKGAGSYILQPGDTVEWLYTLDMGKDVGAEVQ
>NZ_LN831776.1|WP_020433224.1|1285575_1286520_+|energy-coupling-factor-transporter-transmembrane-protein-EcfT
MSSGFRAMHPSAALLYYAGLLLFATLLFHPLFLATELAGLILLLVLQGQGRQLLRGLPFFLLMAVSVAVLNPLFSHRGAHILFYFMDQPVTLEAVLYGLMMMAVLLTVCILFISYSYTVTTDKFMYLFAAAAPRATLLTLMALRFVPLFQRRLRQITMIQRIRGVDAGKGSVRSRMRDGMTLVKVLLTWSLEEALQTADSMKARGYGIRKRSVYGIYRLDLQDKAILLLLAASGLVPLFFWMKGYGVLEIYPRMKPMHFGWADAAMYASFCLFVLTPPALEGKEKWLWRSSRRSVYPSAIPRKTGTRFMSSHLR
>NZ_LN831776.1|WP_020433225.1|1286435_1288118_+|ATP-binding-cassette-domain-containing-protein
MEILAAERLSFSYPEEDRDSLHELSFTVEEGEFVVLLGPSGGGKTTLLRHLKRELAPVGKAGGKIAYKGQPLSGLPAELAAAEIGMVFQNPDAQIVMDTVWHELAFSMENMGYPPAVMRSRLAEIAGLFGLEPLLYKSVHELSGGQKQLLNLASVLMLQPKLLLLDEPTSQLDPVAAREFLQTLHRLNEEMSVTVIISEHRLEEVLPLADRVLLLEEGELRFQGTPRDFVRGAGLALHAPHMAYLPTAARLFLALEPDAVQAPREAIPLTVREGKRWLHSLAERGPGMGEAAADTGASRLSAPVTSSDLLLSCREVTFRYSKDGAEVLKKLSLSLYRGELLAVMGGNGAGKSTLLHILNGLLKPQRGKVTLAKGETSGFLAQNPLLYFSYDTVQEELQQMAEYAGLSKEEADREIARLLAIFQLEDLLLSHPHDISGGQQQKLALAMVMLLGPGILLLDEPTKGLDPGAKERLAALLGDLRRQGVSILLVTHDVEFAARYASRCAMLFDGGITSEGTPAEFFSSNYFYTTAVNRMARELLPQALTIEDVMNAWSAFASRS

Crispr_ID: NZ_LN831776_18

• CRISPR_ID: NZ_LN831776_18
• CRISPR_location: 1296088-1296161
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_18

Consensus_repeat	Method
AATTAGTGTCCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_18

>18.1|1296111|28|NZ_LN831776|CRISPRCasFinder
CATCTGCCCGAGGGTAGGTACTTCGACA

CRISPR arrays and Neighbor proteins around NZ_LN831776_18

CRISPR arrays

The CRISPR arrays of NZ_LN831776_18

>merge|NZ_LN831776|18|1296088-1296161|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTTCATCTGCCCGAGGGTAGGTACTTCGACAAATTAGTGTCCCTTTTTCCACTT

>NZ_LN831776|18|18|1296088-1296161|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTT	CATCTGCCCGAGGGTAGGTACTTCGACA
AATTAGTGTCCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020433227.1|1288090_1288777_+|ECF-transporter-S-component	unknown	unknown	gnl|CDD|377783
NZ_LN831776.1|WP_046501370.1|1284640_1285579_+|DUF4430-domain-containing-protein	unknown	unknown	gnl|CDD|379618
NZ_LN831776.1|WP_020433231.1|1291102_1291423_+|PadR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224609
NZ_LN831776.1|WP_167345586.1|1306067_1308128_+|hypothetical-protein	unknown	unknown	gnl|CDD|223912
NZ_LN831776.1|WP_039789491.1|1296280_1296571_-|cytochrome-aa3-quinol-oxidase-subunit-IV	unknown	unknown	gnl|CDD|200218
NZ_LN831776.1|WP_020433224.1|1285575_1286520_+|energy-coupling-factor-transporter-transmembrane-protein-EcfT	unknown	unknown	gnl|CDD|223692
NZ_LN831776.1|WP_020429753.1|1296575_1297172_-|cytochrome-(ubi)quinol-oxidase-subunit-III	unknown	unknown	gnl|CDD|239214
NZ_LN831776.1|WP_020429748.1|1302186_1302804_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_LN831776.1|WP_020433233.1|1291419_1291977_+|DUF1700-domain-containing-protein	unknown	unknown	gnl|CDD|285278
NZ_LN831776.1|WP_085981603.1|1301010_1301811_+|polysaccharide-deacetylase	unknown	unknown	gnl|CDD|200569
NZ_LN831776.1|WP_020429743.1|1305199_1306102_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224054
NZ_LN831776.1|WP_020433225.1|1286435_1288118_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213192
NZ_LN831776.1|WP_046501377.1|1293862_1295497_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020429752.1|1297168_1299115_-|cytochrome-aa3-quinol-oxidase-subunit-I	unknown	unknown	gnl|CDD|131928
NZ_LN831776.1|WP_020433234.1|1291973_1292918_+|DUF4097-family-beta-strand-repeat-protein	unknown	unknown	gnl|CDD|372574
NZ_LN831776.1|WP_046501383.1|1302975_1304673_+|MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_LN831776.1|WP_020429750.1|1299154_1300174_-|cytochrome-aa3-quinol-oxidase-subunit-II	unknown	unknown	gnl|CDD|273621
NZ_LN831776.1|WP_020429744.1|1304816_1305197_+|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224639
NZ_LN831776.1|WP_020433229.1|1289211_1290723_+|methyl-accepting-chemotaxis-protein	unknown	unknown	gnl|CDD|378936
NZ_LN831776.1|WP_039790900.1|1292987_1293866_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213231

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020433227.1|1288090_1288777_+|ECF-transporter-S-component	gnl|CDD|377783	pfam07155, ECF-ribofla_trS, ECF-type riboflavin transporter, S component. This family is the substrate-binding component (S component) of the energy coupling-factor (ECF)-type riboflavin transporter. It is a transmembrane protein which binds riboflavin, and is responsible for riboflavin-uptake by cells.	1.88639e-08
NZ_LN831776.1|WP_046501370.1|1284640_1285579_+|DUF4430-domain-containing-protein	gnl|CDD|379618	pfam14478, DUF4430, Domain of unknown function (DUF4430). Although this family has overlaps with SLBB, the majority of its sequences are unique. Several family members, eg UniProtKB:A0RGA8, that do not overlap have an LPXTG-cell wall anchor at their C-terminus, a SSF_Family 10_polysaccharide_lyase or Glycosyltransferase structure associated with them in the middle region, as shown by InterPro, as well as this domain at the N-terminus.	1.03865e-19
NZ_LN831776.1|WP_020433231.1|1291102_1291423_+|PadR-family-transcriptional-regulator	gnl|CDD|224609	COG1695, COG1695, Predicted transcriptional regulators [Transcription].	1.17192e-21
NZ_LN831776.1|WP_167345586.1|1306067_1308128_+|hypothetical-protein	gnl|CDD|223912	COG0842, COG0842, ABC-type multidrug transport system, permease component [Defense mechanisms].	0.0033281
NZ_LN831776.1|WP_039789491.1|1296280_1296571_-|cytochrome-aa3-quinol-oxidase-subunit-IV	gnl|CDD|200218	TIGR02901, cytochrome_aa3_quinol_oxidase_subunit_IV, cytochrome aa3 quinol oxidase, subunit IV. This family (QoxD) encodes subunit IV of the aa3-type quinone oxidase, one of several bacterial terminal oxidases. This complex couples oxidation of reduced quinones with the reduction of molecular oxygen to water and the pumping of protons to form a proton gradient utilized for ATP production. aa3-type oxidases contain two heme a cofactors as well as copper atoms in the active site. [Energy metabolism, Electron transport].	1.83976e-23
NZ_LN831776.1|WP_020433224.1|1285575_1286520_+|energy-coupling-factor-transporter-transmembrane-protein-EcfT	gnl|CDD|223692	COG0619, CbiQ, ABC-type cobalt transport system, permease component CbiQ and related transporters [Inorganic ion transport and metabolism].	2.43318e-11
NZ_LN831776.1|WP_020429753.1|1296575_1297172_-|cytochrome-(ubi)quinol-oxidase-subunit-III	gnl|CDD|239214	cd02863, Ubiquinol_oxidase_III, Ubiquinol oxidase subunit III subfamily. Ubiquinol oxidase, the terminal oxidase in the respiratory chains of aerobic bacteria, is a multi-chain transmembrane protein located in the cell membrane. It catalyzes the reduction of O2 and simultaneously pumps protons across the membrane. Ubiquinol oxidases feature four subunits in contrast to the 13 subunit bovine cytochrome c oxidase (CcO). Subunits I, II, and III of bovine CcO are encoded within the mitochondrial genome and the remaining 10 subunits are encoded within the nuclear genome. Subunits I, II and III of ubiquinol oxidase are homologous to the corresponding subunits in bovine CcO. Although not required for catalytic activity, subunit III appears to be involved in assembly of the multimer complex.	2.03863e-79
NZ_LN831776.1|WP_020433233.1|1291419_1291977_+|DUF1700-domain-containing-protein	gnl|CDD|285278	pfam08006, DUF1700, Protein of unknown function (DUF1700). This family contains many hypothetical bacterial proteins and putative membrane proteins.	7.09715e-40
NZ_LN831776.1|WP_085981603.1|1301010_1301811_+|polysaccharide-deacetylase	gnl|CDD|200569	cd10944, CE4_SmPgdA_like, Catalytic NodB homology domain of Streptococcus mutans polysaccharide deacetylase PgdA, Bacillus subtilis YheN, and similar proteins. This family is represented by a putative polysaccharide deacetylase PgdA from the oral pathogen Streptococcus mutans (SmPgdA) and Bacillus subtilis YheN (BsYheN), which are members of the carbohydrate esterase 4 (CE4) superfamily. SmPgdA is an extracellular metal-dependent polysaccharide deacetylase with a typical CE4 fold, with metal bound to a His-His-Asp triad. It possesses de-N-acetylase activity toward a hexamer of chitooligosaccharide N-acetylglucosamine, but not shorter chitooligosaccharides or a synthetic peptidoglycan tetrasaccharide. SmPgdA plays a role in tuning cell surface properties and in interactions with (salivary) agglutinin, an essential component of the innate immune system, most likely through deacetylation of an as-yet-unidentified polysaccharide. SmPgdA shows significant homology to the catalytic domains of peptidoglycan deacetylases from Streptococcus pneumoniae (SpPgdA) and Listeria monocytogenes (LmPgdA), both of which are involved in the bacterial defense mechanism against human mucosal lysozyme. The Bacillus subtilis genome contains six polysaccharide deacetylase gene homologs: pdaA, pdaB (previously known as ybaN), yheN, yjeA, yxkH and ylxY. The biological function of BsYheN is still unknown. This family also includes many uncharacterized polysaccharide deacetylases mainly found in bacteria.	6.10627e-87
NZ_LN831776.1|WP_020429743.1|1305199_1306102_+|ABC-transporter-ATP-binding-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	3.93658e-73
NZ_LN831776.1|WP_020433225.1|1286435_1288118_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|213192	cd03225, ABC_cobalt_CbiO_domain1, First domain of the ATP-binding cassette component of cobalt transport system. Domain I of the ABC component of a cobalt transport family found in bacteria, archaea, and eukaryota. The transition metal cobalt is an essential component of many enzymes and must be transported into cells in appropriate amounts when needed. This ABC transport system of the CbiMNQO family is involved in cobalt transport in association with the cobalamin (vitamin B12) biosynthetic pathways. Most of cobalt (Cbi) transport systems possess a separate CbiN component, the cobalt-binding periplasmic protein, and they are encoded by the conserved gene cluster cbiMNQO. Both the CbiM and CbiQ proteins are integral cytoplasmic membrane proteins, and the CbiO protein has the linker peptide and the Walker A and B motifs commonly found in the ATPase components of the ABC-type transport systems.	6.14226e-84
NZ_LN831776.1|WP_020429748.1|1302186_1302804_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	8.9535e-13
NZ_LN831776.1|WP_020429752.1|1297168_1299115_-|cytochrome-aa3-quinol-oxidase-subunit-I	gnl|CDD|131928	TIGR02882, cytochrome_aa3_quinol_oxidase_subunit_I, cytochrome aa3 quinol oxidase, subunit I. This family (QoxB) encodes subunit I of the aa3-type quinone oxidase, one of several bacterial terminal oxidases. This complex couples oxidation of reduced quinones with the reduction of molecular oxygen to water and the pumping of protons to form a proton gradient utilized for ATP production. aa3-type oxidases contain two heme a cofactors as well as copper atoms in the active site. [Energy metabolism, Electron transport].	0
NZ_LN831776.1|WP_020433234.1|1291973_1292918_+|DUF4097-family-beta-strand-repeat-protein	gnl|CDD|372574	pfam13349, DUF4097, Putative adhesin. This has a putative all-beta structure with a twenty-residue repeat with a highly conserved repeating GD, gly-asp, motif. It may form part of a bacterial adhesin.	5.06618e-17
NZ_LN831776.1|WP_046501383.1|1302975_1304673_+|MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	7.70478e-69
NZ_LN831776.1|WP_020429750.1|1299154_1300174_-|cytochrome-aa3-quinol-oxidase-subunit-II	gnl|CDD|273621	TIGR01432, AA3-600_quinol_oxidase_subunit_II, cytochrome aa3 quinol oxidase, subunit II. This enzyme catalyzes the oxidation of quinol with the concomitant reduction of molecular oxygen to water. This acts as the terminal electron acceptor in the respiratory chain. This subunit contains two transmembrane helices and a large external domain responsible for the binding and oxidation of quinol. QuoX is (presently) only found in gram positive bacteria of the Bacillus/Staphylococcus group. Like CyoA, the ubiquinol oxidase found in proteobacteria, the residues responsible for the ligation of Cu(a) and cytochrome c (found in the related cyt. c oxidases) are absent. Unlike CyoA, QoxA is in complex with a subunit I which contains cytochromes a similar to the cyt. c oxidases (as opposed to cytochromes b). [Energy metabolism, Electron transport].	1.68195e-87
NZ_LN831776.1|WP_020429744.1|1304816_1305197_+|GntR-family-transcriptional-regulator	gnl|CDD|224639	COG1725, COG1725, Predicted transcriptional regulators [Transcription].	3.89665e-37
NZ_LN831776.1|WP_020433229.1|1289211_1290723_+|methyl-accepting-chemotaxis-protein	gnl|CDD|378936	pfam12729, 4HB_MCP_1, Four helix bundle sensory module for signal transduction. This family is a four helix bundle that operates as a ubiquitous sensory module in prokaryotic signal-transduction. The 4HB_MCP is always found between two predicted transmembrane helices indicating that it detects only extracellular signals. In many cases the domain is associated with a cytoplasmic HAMP domain suggesting that most proteins carrying the bundle might share the mechanism of transmembrane signalling which is well-characterized in E coli chemoreceptors.	1.54259e-22
NZ_LN831776.1|WP_039790900.1|1292987_1293866_+|ABC-transporter-ATP-binding-protein	gnl|CDD|213231	cd03264, ABC_drug_resistance_like, ABC-type multidrug transport system, ATPase component. The biological function of this family is not well characterized, but display ABC domains similar to members of ABCA subfamily. ABC transporters are a large family of proteins involved in the transport of a wide variety of different compounds, like sugars, ions, peptides, and more complex organic molecules. The nucleotide binding domain shows the highest similarity between all members of the family. ABC transporters are a subset of nucleotide hydrolases that contain a signature motif, Q-loop, and H-loop/switch region, in addition to, the Walker A motif/P-loop and Walker B motif commonly found in a number of ATP- and GTP-binding and hydrolyzing proteins.	3.42194e-110

Protein sequences

>NZ_LN831776.1|WP_046501377.1|1293862_1295497_+|hypothetical-protein
MSKVHTIYHLARADFLERTRRYSFFVTAVLAVFAAYLFVPPADSNYVTFYLGNYRGVYNSAWVGGTVAVSTTMFLTLVGFFLVKNSIDRDLRTRVGFIISGTPLKKRHYLLGKALSNFAVLSVIAFLMMVVALLMQLIRGEDMTIHILDIVLPFLIVVFPQLAVVAALAVVFESRTLLRGAAGNLIYLALFIATVTISINNGNLSTGIISGQMQNDLKQINPAYDGEFGQGIMFLDKPLSLFQWHGMHWSGSIVGMQLLLFAAALALCLLAALLFKGFAELPASRQGQAYSRRSRRAGPEKKAVSPLSGESEQSQQAAANAPGLPAAALTPVVYRFRFMALVKAELGLMLKGSSWLWFAVGAALNILCLLLPLDNSFSFFWPLAWIWPLTLWSAMGCREVMHGTHLFLAASPKLIARQLPAIWAAGYIVTAAAGGGILVRLLIEGDMVHALYWLLGSLFIPTLALVSGVITHSKKLFEVLYMLLWYIGPFNQAPGVNFLGTDLPARSLGQAGFSAWLPLAVCFALTVVLLISAFVGRRRLAAVH
>NZ_LN831776.1|WP_039790900.1|1292987_1293866_+|ABC-transporter-ATP-binding-protein
MVLVIEKVGKRYNKNFWGIKDINLELKEGIIGLLGPNGAGKSTLMRILATISQPTQGRVTWNGRDLAAHPDELRRVLGYLPQDFGVYPNLTAVEFLQYMAAVKGLDGSRANRRIDELLELLNLNGARKRKIGGYSGGMKQRIGIAQALLNDPKVLIVDEPTVGLDPEERMRFRNLLADLSQGRIILFSTHIVSDIEATADRIVILAKSRLLADAPPSQLLKLAEGKVWSTVIPENQLQEARSKWLISGSVRIGEGVRVRMVAGEAPAPDAVQVAPDLEDAYLFLRSGLGDSQ
>NZ_LN831776.1|WP_020433234.1|1291973_1292918_+|DUF4097-family-beta-strand-repeat-protein
MKKWIITAVVLFVVGLIGVTATMWNEGGFSLGSVEVNQEQAVAADGVKDVVLSLNSINVTMVKGTANEIKASLAGRVSKKMVESTKLNLIREGDTVKIGVDSNRWTVGFSVFDVQVRVELPQQQYESFVFNSGTGDMNIAGVSARSVRVEADSGTVKLEGMKAGKISLELGSGDIEVNNVAADTLELNGDSTDVFLGKLAAQKVKLKTGGGNIRMKDVEAELELEADTGEVEAEMTDITHPINITTGSGEVILNTAERPSSAAIRFSHGSGELHNQWEGTAQTTAHEGDDIVFGDGSVAVNVKTGSGDLTLGKR
>NZ_LN831776.1|WP_020433233.1|1291419_1291977_+|DUF1700-domain-containing-protein
MTQEQFLTQLRELMNPIPEPLRSEWIFDYEEHFRQAVEEGLREEQITEELGDPRQLAKEMVLAYRVNQAESSNGRLAPVSRVVFAMVGLGLFNLVFVLAPYIMLLAVLLVCWTSAAASGLVALTAIYEGVIGDAFTPVQGVFVAVMLLGAGMLLGAFSRWLTMAVSRMTLRYLKFNSKVMRVKGS
>NZ_LN831776.1|WP_020433231.1|1291102_1291423_+|PadR-family-transcriptional-regulator
MNIQFKKGVLDLCVLALTAREDRYGYELAVAISSKFEVAVGSVYPLLNRLTLEGYFSTYLRESREGPPRKYYKLTALGQNHLEELILEWRSFTVSVDQLIKEGVEG
>NZ_LN831776.1|WP_020433229.1|1289211_1290723_+|methyl-accepting-chemotaxis-protein
MRHLKVRHKMLLLVTVFIIMLIGTGAVGIITTKQMATGSGKSYSQNLQPMYLITEIRGNNRAIESLLLESLITKNDGKSQEHTAAIGEYININNELITQLKAISFSNKDVSNKINEYLSLLPDYRAQRDSIVQLAGKKLKNEGYQIFSGSVFSKSREIMVSLLEDTAKLLVQDARNNNETNQQDAQRSLTLIILLIIAALVLSIGISILISRMITKPLKELQVLMKDAESGNLTASAAYSSRDETGQLHRSFNAMIQSLKTMMQGVSESTGLLSASSQEMSASAEQAAQASQFIAESSSAIAAGIGVQVETVDRAAHSVQAMAEEIAAARQSTHEISGLMAAAAASADHGAAAVEVILAQLKEIAEATGKSSLQITDLLTQIQSQTEEAVQSIIRDSQLVSQGLSQSGAVPRVFAEIQESIRTAARQTAELREAIGHVSGQALTVSQAMGQASEASRKSAEDVQNLSRASEEQVTAMGEMLMSSRYLAALAENLHMNLARFKL
>NZ_LN831776.1|WP_020433227.1|1288090_1288777_+|ECF-transporter-S-component
MVRFRFPLLIALGLFVAGLALTSALKDRHYMLLSLVLLAVALLPLFIRLERRPLESRELVLLAVLSAVAAVSRIPFAALPSVKPVSAIVILSAYVFGAEAGFIIGAVAALVSNIYFGQGPWTPWQMFAWGMVGLTAGWLRNTWWMKKKGGMLAFGFVWGFLFGWIMNIWYLISLPDAFSWGLVAAAYASSFYLDLAHALSNVFFLAVLAGGWTKVLKRFRKKYGLLQE
>NZ_LN831776.1|WP_020433225.1|1286435_1288118_+|ATP-binding-cassette-domain-containing-protein
MEILAAERLSFSYPEEDRDSLHELSFTVEEGEFVVLLGPSGGGKTTLLRHLKRELAPVGKAGGKIAYKGQPLSGLPAELAAAEIGMVFQNPDAQIVMDTVWHELAFSMENMGYPPAVMRSRLAEIAGLFGLEPLLYKSVHELSGGQKQLLNLASVLMLQPKLLLLDEPTSQLDPVAAREFLQTLHRLNEEMSVTVIISEHRLEEVLPLADRVLLLEEGELRFQGTPRDFVRGAGLALHAPHMAYLPTAARLFLALEPDAVQAPREAIPLTVREGKRWLHSLAERGPGMGEAAADTGASRLSAPVTSSDLLLSCREVTFRYSKDGAEVLKKLSLSLYRGELLAVMGGNGAGKSTLLHILNGLLKPQRGKVTLAKGETSGFLAQNPLLYFSYDTVQEELQQMAEYAGLSKEEADREIARLLAIFQLEDLLLSHPHDISGGQQQKLALAMVMLLGPGILLLDEPTKGLDPGAKERLAALLGDLRRQGVSILLVTHDVEFAARYASRCAMLFDGGITSEGTPAEFFSSNYFYTTAVNRMARELLPQALTIEDVMNAWSAFASRS
>NZ_LN831776.1|WP_020433224.1|1285575_1286520_+|energy-coupling-factor-transporter-transmembrane-protein-EcfT
MSSGFRAMHPSAALLYYAGLLLFATLLFHPLFLATELAGLILLLVLQGQGRQLLRGLPFFLLMAVSVAVLNPLFSHRGAHILFYFMDQPVTLEAVLYGLMMMAVLLTVCILFISYSYTVTTDKFMYLFAAAAPRATLLTLMALRFVPLFQRRLRQITMIQRIRGVDAGKGSVRSRMRDGMTLVKVLLTWSLEEALQTADSMKARGYGIRKRSVYGIYRLDLQDKAILLLLAASGLVPLFFWMKGYGVLEIYPRMKPMHFGWADAAMYASFCLFVLTPPALEGKEKWLWRSSRRSVYPSAIPRKTGTRFMSSHLR
>NZ_LN831776.1|WP_046501370.1|1284640_1285579_+|DUF4430-domain-containing-protein
MSKSIQQWLFTPLLLLSAAVLLAGCAAGADTAGGAQSPAAGTAAVQSPQPKTPASPLPGDAATPVPSAAADGTAPPSGAEPAAGTQKGAAVSAPPASSGAAAKPAPSAAAVTEPASVTASAAPATAKASAGPAKPAAGAKPTASTKPAAGAKPTASTKPTAGAQPAAGTKPAATAKPAATAQAPAAASAAPAKPAGAVNTVTLSIVGDKEHGTIFAAAAVDIKSGESALELLKRITRSNKIQMEYQGAKSFAYVEGIDNLYEFDQGPESGWIYKVNGEVPGKGAGSYILQPGDTVEWLYTLDMGKDVGAEVQ
>NZ_LN831776.1|WP_039789491.1|1296280_1296571_-|cytochrome-aa3-quinol-oxidase-subunit-IV
MKQLFPIRHVMGYLASLVLSAAALIVIYGDLSKGANMAVLLVTAIIQASLQLFVFMHIGEAADTKKELYINIAYALFVGLVTIFGTLYIFVWGWYA
>NZ_LN831776.1|WP_020429753.1|1296575_1297172_-|cytochrome-(ubi)quinol-oxidase-subunit-III
MKIDASKPLEYSTEENSNKIFGFWVFLGAEIPLFATLFTVYFVMVDRFASGPSGSELFEIGPVLIETFLLLTSSFTIGLAVHAMRLGYKKAMMVLMAITLLMGLGFIGIEIDEFFTYVHEGATLQTSGFLSSLFVLLGTHGAHVSFGFLWGTAIMIQVWRQGINPATANKAFIFSLFWHFLDVVWIFIFSFVYLKGLM
>NZ_LN831776.1|WP_020429752.1|1297168_1299115_-|cytochrome-aa3-quinol-oxidase-subunit-I
MDLDKFKVHGEPLIYGAMVSIALATIGILVGLTYFKKWGYLWREWLTTVDHKKIGVMYILAALLMLFRGGVDAIMMRLQTAAPEMKFLDAQHYNEVFTTHGLIMILFMAMPFIIGLMNVIVPLQIGARDVAFPRLNAVSFWLFFFGAMLLNISFVIGGSPDAGWSAYFPLASLEFSPTVGNNYYSLALQISGIGTLITGVNFIVTILKMRAPGMKLMKMPMFTWSVLITNVIIVFAFPVLTVALALMMFDRLFGSQFFTMANGGMDMLWANLFWVWGHPEVYIVILPAFGIYSEIIATFSKKNLYGYTSMVFSMLIISLLSFLVWAHHFYTMGQGAMVNSFFSITTMAIAVPTGVKIFNWLFTLRKGRITFTTPMLYTLAFIPIFTIGGVTGVMLAMASADYQYHNTMFLVAHFHYVLIPGAVFAVIAGFHYWFPKVFGFRLNERLGKHSFWWIVISFNVTFFPLFFLGLMGMTRRMYTYSEESGFGPLNMLSFVGAVGLAIGFVLLVYNIYWSTRYMPRDTTSDPWDGRTLEWATHSPMPVYNFAVVPKVQTRDAFWSAKQDNMPLFEDKITKIHMPSNTGKPFILGVIFFFLGFFLVFSMWIPAIVAGVGVLIMLAAMSFDRDHGYYISVDEVMATEKKLMRGETV
>NZ_LN831776.1|WP_020429750.1|1299154_1300174_-|cytochrome-aa3-quinol-oxidase-subunit-II
MKKKGPLYALFLSLILLLPGCSSLTVLNPKGPSARTLSDTIILSILVMLGVLAVVYILYIFVLVKYRAKKSNEGYIPEHEEGNKVLETIWIVIPIIIVAFLSVVTVKTTNAVENQAVEYKDQTPLVIYAASSNWKWHFSYPEEGIETVNYVNMPVHRAVEFRMYSFGSITSLWIPQLAGQKYAMSDMLTTLHLSADTEGSYMGRNANFSGKGFAHMEFEALVMSSKDYDDWVKEVKETAPKLTEKEFKGLLATDYLGRKTYSSTHLEFSPPPGEHSEHMSGGGKEMDMDNGSMEHQDNKEIHPSPEPSSETEFDSKPNPEVEQPLPSSPVDEHTHDSNS
>NZ_LN831776.1|WP_085981603.1|1301010_1301811_+|polysaccharide-deacetylase
MVPLKISAYLGYRISFEPDKYLLRVQDGSAALDDTAFVSKYKNELAPPAPAEPAQNPPAAKPGKTLYLTFDDGPSATTPELLDILNKYGVKATFFMLGPNMNRYPSQVKRIAEEGNGLGLHGMTHRKEKFYASASAALAEMNGDNDVLRKITGTGTTLIRPPYGSKPYFTKAFRDKVLGQGYHLWDWNVDSDDWKYKEDSVTIYNTVMGQVHKLQKSKTNPVILMHDQKATLKVLPRLLESLKKEGYTFGIITKDMEPVNFWKDKR
>NZ_LN831776.1|WP_020429748.1|1302186_1302804_-|TetR/AcrR-family-transcriptional-regulator
MSDMEDKIRTPRQERSIRTREAIVQAAMKQFSDKGFHQTNTKQIAAAAGVSTGSFYSYFVDKRAVFIEVLKNYGTDLLARIDASMSEINFLTIDRSELIMHLVDTLLISHEAFIGYHRELTIMYHSDEEIKQLMDAQYEAGRIRTLEYLQMGQDELKTEDMEAASVIVFETVSAIVDVISFSQQRIATERLKSELVHMIVSYLYK
>NZ_LN831776.1|WP_046501383.1|1302975_1304673_+|MFS-transporter
MSVRMRRALSFTAIVLGFFMALLDTTIINIALPEMTRHFGGSVSRISWVMNGYNLAFAVFILTASRLADQFGRKKVFICGVALFTLTSLLAGFATSLGMLILLRVIQGLAGAIIVPVTIPLTTTTFPKEMHGLIIGIWGAVSGVAAASGPALGGILTQNLSWEWIFFVNVPLGVLSIVLTAVFIQESRDDTAGRSIDYGGTLGITGAMFFITYALIKVQDYGWSSGKTLALLGAGVVFLLLFILTQWKGKEPMLPLSLMRIRTFNSASLTLLIVGAALMNLSLLTSFFLTRMMGMTELKAGLVLSMVAVGSIVSSAVSGPLSAKYGSHLFAAAGIVVTGGAMYSMSGLHADSAVAEVVVRLLVAGVGIGLTMAPVMSSAVRNVPEDKVGISSGVTNMAKSLGSVIGVAIIVTVLQHNMDSELGKAGNHLSEAIQADVKLQPIVKTVLAETAASISKEGAAPMGGTSGKADPAAAVAHAVELAAAKLPPAEQKAFAADSANQLREAKLLLSQAGNGMQQAAVEGFRRTFVFAGLLMIPGILFALLSDKRRKPEEPVAVAEPAVLER
>NZ_LN831776.1|WP_020429744.1|1304816_1305197_+|GntR-family-transcriptional-regulator
MFELDVRSRKPIYEQLNDKVKELIMHGILRADEQLPSVRTLSSQLTVNPNTIQKAYRELEREGYIYSLQGKGSFVAPLQQGQNESKKAELREELLRLMAEAVYLGFTENEIGALYRQVLEQREKGE
>NZ_LN831776.1|WP_020429743.1|1305199_1306102_+|ABC-transporter-ATP-binding-protein
MIEIRGVSKSFQGEKAVDSLSLTVHKGAIYGLLGSNGAGKTTLLKTLAGIYRSEEGTVKIGGQPVFENPQVKQSLIFMPDSPYFFPQASLKTMAAFYRSVYPGFSDKRFEELGTVFRLDMGRKLSRFSKGMQRQAAFWLALSCRPDVLIMDEPIDGLDPVMRRQIKNLLFQEVAERELTVLISSHNLREIEDLCDHVGIMHHGRMLVEKDLDDLKADTHKVQVAFRDERHADALAAKLQILHQERRGSVDLYIVKGDRERISKVIHVYEPYVFDLLPLTLEEIFIYEMGDAGYDAQPILL
>NZ_LN831776.1|WP_167345586.1|1306067_1308128_+|hypothetical-protein
MPGMTRSQYFFNSSVIRQCLRQHGWIGIIYTLGLLFSLPLQLFMSRYPGAEPQKIDTLFRVGGNIQMLFIISLPVAAGLFLFRYLQSRMASDLWHSLPLRREHLLTAHLASGLGLLLLPVWLTAAVTAMVTPMNGNMYIYQGSDIWSWCLTVSILTLFLFVFSIFVGICTGQTVLQGIIIYILLLLPAVLMELVNLHLNRYLYGYPEWFGLNNDRLVWSPLLHLIVLAEEPYSTGELWAYSGLSLVFIVFSYILYRKRSAEKSGQAIAFTYFNPLFKAGVMLCAMLLAGTYFAAVKPHQVGWILCSHFAGALLGYIAAEMIIRKTWHILSRRVPLEFAVYGVLLGLLIYIPVSGLTGYESRVPAAEHITGVYAGSNYRMYNDDSYNRYASGEVAKVSSGSRVPFSGGQQYVEAVRNLHQTLVTMRPDKNAFPLEGYTRGSRMFTLAYQLDNGRKMVREYRIPAQGFEPEMKAVMGNEDFKRAEYDIQALNTEIESFRLSSRNRVVRITEPEDVQEFKDILIREKLNMSYEDQNEGQLPIAYIQPINKPADEEEGSGRAMVTVTRNYEWLPSYKELGNWMEQKGYADKIRTTAQDVKSAEIIKDDYKGKLSPEKIYNVELHMALARQQKLSVVTRDKKLIEGILENQREYAGKNGMYAAKLEYTDGDTQYVSLDGKGLEPALKQLLP

Crispr_ID: NZ_LN831776_19

• CRISPR_ID: NZ_LN831776_19
• CRISPR_location: 1507963-1508057
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_19

Consensus_repeat	Method
AAGTTTTGTAAGCGAAACTCCCGTGAATCC	CRISPRCasFinder

spacers of NZ_LN831776_19

>19.1|1507993|35|NZ_LN831776|CRISPRCasFinder
TGCTTCGTACAAAACTTACTTCGTAAGCATAAGCT

CRISPR arrays and Neighbor proteins around NZ_LN831776_19

CRISPR arrays

The CRISPR arrays of NZ_LN831776_19

>merge|NZ_LN831776|19|1507963-1508057|CRISPRCasFinder
AAGTTTTGTAAGCGAAACTCCCGTGAATCCTGCTTCGTACAAAACTTACTTCGTAAGCATAAGCTAAGTTTTGTGAGCGAAACTCCCGTGAATCC

>NZ_LN831776|19|19|1507963-1508057|CRISPRCasFinder
AAGTTTTGTAAGCGAAACTCCCGTGAATCC	TGCTTCGTACAAAACTTACTTCGTAAGCATAAGCT
AAGTTTTGTGAGCGAAACTCCCGTGAATCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020429787.1|1504591_1505422_+|hypothetical-protein	unknown	unknown	gnl|CDD|270317
NZ_LN831776.1|WP_039789535.1|1517120_1517852_+|glutamine-amidotransferase	unknown	unknown	gnl|CDD|227150
NZ_LN831776.1|WP_020429782.1|1501330_1502239_+|GGDEF-domain-containing-protein	unknown	unknown	gnl|CDD|143635
NZ_LN831776.1|WP_020429788.1|1505446_1506259_+|pyrroline-5-carboxylate-reductase	unknown	unknown	gnl|CDD|223422
NZ_LN831776.1|WP_020429804.1|1514713_1515661_+|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_046501550.1|1499564_1500842_+|IS91-family-transposase	unknown	unknown	gnl|CDD|377437
NZ_LN831776.1|WP_020429805.1|1515668_1516745_+|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_LN831776.1|WP_020429792.1|1507350_1507947_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046501561.1|1510739_1511606_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_039789526.1|1509921_1510740_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_039789524.1|1503524_1504262_-|glycerophosphodiester-phosphodiesterase	unknown	unknown	gnl|CDD|176506
NZ_LN831776.1|WP_020429811.1|1519337_1519847_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831776.1|WP_020425919.1|1498171_1498756_+|histidine-phosphatase-family-protein	unknown	unknown	gnl|CDD|366010
NZ_LN831776.1|WP_020429809.1|1517852_1518821_+|sugar-phosphate-isomerase/epimerase	unknown	unknown	gnl|CDD|224007
NZ_LN831776.1|WP_020429800.1|1511697_1512960_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270452
NZ_LN831776.1|WP_046501545.1|1498761_1499061_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046501557.1|1502263_1503520_-|SLC45-family-MFS-transporter	unknown	unknown	gnl|CDD|340871
NZ_LN831776.1|WP_020429790.1|1506255_1507038_+|VOC-family-protein	unknown	unknown	gnl|CDD|379203
NZ_LN831776.1|WP_020429802.1|1513161_1514166_-|substrate-binding-domain-containing-protein	unknown	unknown	gnl|CDD|380630
NZ_LN831776.1|WP_020429794.1|1508190_1509879_-|alpha-glucosidase	unknown	unknown	gnl|CDD|200472

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020429787.1|1504591_1505422_+|hypothetical-protein	gnl|CDD|270317	cd13599, PBP2_lipoprotein_Gna1946, The membrane-associated lipoprotein Gna1946 from Neisseria meningitidis; the type 2 periplasmic binding protein fold. Gna1946 shares significant structural and sequence homology with the periplasmic substrate-binding domain of ATP-binding cassette (ABC) transporter involved in uptake of methionine (MetQ). The members of the MetQ-like family include the 32-kilodalton lipoprotein (Tp32) from Treponema pallidum, the membrane-associated lipoprotein-9 GmpC from Staphylococcus aureus, and Toll-like receptor 2-activating lipoprotein IlpA from Vibrio vulnificus. They all function as a receptor for methionine. This substrate-binding domain belongs to the type 2 periplasmic binding fold protein superfamily (PBP2). The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea.	2.02406e-77
NZ_LN831776.1|WP_039789535.1|1517120_1517852_+|glutamine-amidotransferase	gnl|CDD|227150	COG4813, ThuA, Trehalose utilization protein [Carbohydrate transport and metabolism].	5.47088e-133
NZ_LN831776.1|WP_020429782.1|1501330_1502239_+|GGDEF-domain-containing-protein	gnl|CDD|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	3.83083e-47
NZ_LN831776.1|WP_020429804.1|1514713_1515661_+|AraC-family-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.11944e-26
NZ_LN831776.1|WP_046501550.1|1499564_1500842_+|IS91-family-transposase	gnl|CDD|377437	pfam04986, Y2_Tnp, Putative transposase. Transposases are needed for efficient transposition of the insertion sequence or transposon DNA. This family includes transposases IS1294 and IS801. This is a rolling-circle transposase.	8.32556e-38
NZ_LN831776.1|WP_020429805.1|1515668_1516745_+|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	5.72191e-77
NZ_LN831776.1|WP_039789524.1|1503524_1504262_-|glycerophosphodiester-phosphodiesterase	gnl|CDD|176506	cd08563, GDPD_TtGDE_like, Glycerophosphodiester phosphodiesterase domain of Thermoanaerobacter tengcongensis and similar proteins. This subfamily corresponds to the glycerophosphodiester phosphodiesterase domain (GDPD) present in Thermoanaerobacter tengcongensis glycerophosphodiester phosphodiesterase (TtGDE, EC 3.1.4.46) and its uncharacterized homologs. Members in this family show high sequence similarity to Escherichia coli GP-GDE, which catalyzes the degradation of glycerophosphodiesters to produce sn-glycerol-3-phosphate (G3P) and the corresponding alcohols. Despite the fact that most of GDPD family members exist as the monomer, TtGDE can function as a dimeric unit. Its catalytic mechanism is based on the general base-acid catalysis, which is similar to that of phosphoinositide-specific phospholipases C (PI-PLCs, EC 3.1.4.11). A divalent metal cation is required for the enzyme activity of TtGDE.	1.49201e-115
NZ_LN831776.1|WP_046501561.1|1510739_1511606_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.42472e-74
NZ_LN831776.1|WP_039789526.1|1509921_1510740_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	3.33287e-64
NZ_LN831776.1|WP_020429788.1|1505446_1506259_+|pyrroline-5-carboxylate-reductase	gnl|CDD|223422	COG0345, ProC, Pyrroline-5-carboxylate reductase [Amino acid transport and metabolism].	4.37281e-67
NZ_LN831776.1|WP_020429811.1|1519337_1519847_-|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	1.51615e-17
NZ_LN831776.1|WP_020425919.1|1498171_1498756_+|histidine-phosphatase-family-protein	gnl|CDD|366010	pfam00300, His_Phos_1, Histidine phosphatase superfamily (branch 1). The histidine phosphatase superfamily is so named because catalysis centers on a conserved His residue that is transiently phosphorylated during the catalytic cycle. Other conserved residues contribute to a 'phosphate pocket' and interact with the phospho group of substrate before, during and after its transfer to the His residue. Structure and sequence analyses show that different families contribute different additional residues to the 'phosphate pocket' and, more surprisingly, differ in the position, in sequence and in three dimensions, of a catalytically essential acidic residue. The superfamily may be divided into two main branches. The larger branch 1 contains a wide variety of catalytic functions, the best known being fructose 2,6-bisphosphatase (found in a bifunctional protein with 2-phosphofructokinase) and cofactor-dependent phosphoglycerate mutase. The latter is an unusual example of a mutase activity in the superfamily: the vast majority of members appear to be phosphatases. The bacterial regulatory protein phosphatase SixA is also in branch 1 and has a minimal, and possible ancestral-like structure, lacking the large domain insertions that contribute to binding of small molecules in branch 1 members.	3.15449e-58
NZ_LN831776.1|WP_020429809.1|1517852_1518821_+|sugar-phosphate-isomerase/epimerase	gnl|CDD|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	3.11862e-47
NZ_LN831776.1|WP_020429800.1|1511697_1512960_-|extracellular-solute-binding-protein	gnl|CDD|270452	cd14749, PBP2_XBP1_like, The periplasmic-binding component of ABC transport systems specific for xylo-oligosaccharides; possesses type 2 periplasmic binding fold. This group represents the periplasmic component of an ABC transport system XBP1 that shows preference for xylo-oligosaccharides in the order of xylotriose > xylobiose > xylotetraose. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	9.49267e-49
NZ_LN831776.1|WP_046501557.1|1502263_1503520_-|SLC45-family-MFS-transporter	gnl|CDD|340871	cd17313, MFS_SLC45_SUC, Solute carrier family 45 and similar sugar transporters of the Major Facilitator Superfamily of transporters. This group includes the solute carrier 45 (SLC45) family as well as plant sucrose transporters (SUCs or SUTs) and similar proteins such as Schizosaccharomyces pombe general alpha-glucoside permease. the SLC45 family is composed of four (A1-A4) vertebrate proteins as well as related insect proteins such as Drosophila sucrose transporter SCRT or Slc45-1. Members of this group transport sucrose and other sugars like maltose into the cell, with the concomitant uptake of protons (symport system). Plant sucrose transporters are crucial to carbon partitioning, playing a key role in phloem loading/unloading. They play a key role in loading and unloading of sucrose into the phloem and as a result, they control sucrose distribution throughout the whole plant and drive the osmotic flow system in the phloem. They also play a role in the exchange of sucrose between beneficial symbionts (mycorrhiza and Rhizobium) as well as pathogens such as nematodes and parasitic fungi. There are nine sucrose transporter genes in Arabidopsis and five in rice. Vertebrate SLC45 family proteins have been implicated in the regulation of glucose homoeostasis in the brain (SLC45A1), with skin and hair pigmentation (SLC45A2), and with prostate cancer and myelination (SLC45A3). Mutations in SLC45A2, also called MATP (membrane-associated transporter protein) or melanoma antigen AIM1, cause oculocutaneous albinism type 4 (OCA4), an autosomal recessive disorder of melanin biosynthesis that results in congenital hypopigmentation of ocular and cutaneous tissues. The SLC45 family and related sugar transporters belong to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.49927e-104
NZ_LN831776.1|WP_020429790.1|1506255_1507038_+|VOC-family-protein	gnl|CDD|379203	pfam13468, Glyoxalase_3, Glyoxalase-like domain. This domain is related to the Glyoxalase domain pfam00903.	6.07661e-38
NZ_LN831776.1|WP_020429802.1|1513161_1514166_-|substrate-binding-domain-containing-protein	gnl|CDD|380630	cd19975, PBP1_CcpA-like, ligand-binding domain of putative DNA transcription regulators highly similar to that of the catabolite control protein A (CcpA), which functions as the major transcriptional regulator of carbon catabolite repression/regulation. This group includes the ligand-binding domain of uncharacterized DNA transcription repressors highly similar to that of the catabolite control protein A (CcpA), which functions as the major transcriptional regulator of carbon catabolite repression/regulation (CCR), a process in which enzymes necessary for the metabolism of alternative sugars are inhibited in the presence of glucose. In gram-positive bacteria, CCR is controlled by HPr, a phosphoenolpyruvate:sugar phsophotrasnferase system (PTS) and a transcriptional regulator CcpA. Moreover, CcpA can regulate sporulation and antibiotic resistance as well as play a role in virulence development of certain pathogens such as the group A streptococcus. The ligand binding domain of CcpA is a member of the LacI-GalR family of bacterial transcription regulators.	2.90767e-131
NZ_LN831776.1|WP_020429794.1|1508190_1509879_-|alpha-glucosidase	gnl|CDD|200472	cd11333, AmyAc_SI_OligoGlu_DGase, Alpha amylase catalytic domain found in Sucrose isomerases, oligo-1,6-glucosidase (also called isomaltase; sucrase-isomaltase; alpha-limit dextrinase), dextran glucosidase (also called glucan 1,6-alpha-glucosidase), and related proteins. The sucrose isomerases (SIs) Isomaltulose synthase (EC 5.4.99.11) and Trehalose synthase (EC 5.4.99.16) catalyze the isomerization of sucrose and maltose to produce isomaltulose and trehalulose, respectively. Oligo-1,6-glucosidase (EC 3.2.1.10) hydrolyzes the alpha-1,6-glucosidic linkage of isomaltooligosaccharides, pannose, and dextran. Unlike alpha-1,4-glucosidases (EC 3.2.1.20), it fails to hydrolyze the alpha-1,4-glucosidic bonds of maltosaccharides. Dextran glucosidase (DGase, EC 3.2.1.70) hydrolyzes alpha-1,6-glucosidic linkages at the non-reducing end of panose, isomaltooligosaccharides and dextran to produce alpha-glucose.The common reaction chemistry of the alpha-amylase family enzymes is based on a two-step acid catalytic mechanism that requires two critical carboxylates: one acting as a general acid/base (Glu) and the other as a nucleophile (Asp). Both hydrolysis and transglycosylation proceed via the nucleophilic substitution reaction between the anomeric carbon, C1 and a nucleophile. Both enzymes contain the three catalytic residues (Asp, Glu and Asp) common to the alpha-amylase family as well as two histidine residues which are predicted to be critical to binding the glucose residue adjacent to the scissile bond in the substrates. The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase.	0

Protein sequences

>NZ_LN831776.1|WP_020429792.1|1507350_1507947_-|hypothetical-protein
MLNFLMYLFALLGVSLLLAAGILQIKLSSASSARNKPASGLTPFNYNFTEQYITPDKSHIIALDEKGKQMAVGFCNPASPEAASPAMFPFEHILGSEIVEKALTLTKVSKTSRITTSPARQTPGAAPSGTTAINLDTDHAEEITELTLIIYLNSADTPVLSIPFLPGLTPAKKSDSQYSQALCTARQVHEMIRGIVSA
>NZ_LN831776.1|WP_020429790.1|1506255_1507038_+|VOC-family-protein
MSSLQWDHTVHYINDLEQAVQTFTDNGLAAFPGGSHKLWGTHNALSYFGLNYVEFLAVENRELAESADTANLVVKDAVKLLPEHEGFSRVAIRTDDIEQTAALLQQQGLKLSPIMDGRRLNKQGQWIEWRMLTIGGHFQGLVYPFVIQWKGTDGQRQQELRTAGIIRPHPAGAVEVRAAVFSVTDPAATAAHWSQVIGLPFQNHRSAADGSVSLAIGNKAFVFRQGNGEQMQELLLATDAPGLAGRRIRFGQADYVFTAL
>NZ_LN831776.1|WP_020429788.1|1505446_1506259_+|pyrroline-5-carboxylate-reductase
MAAKRIHFIGGGQMAEAIIRAVIGKGAYKAEQISVADVNEERNLYLKNTYGIHAAVSQAAELGEAELIIIAVRPQDDLAAVGRLIAEHAAGQAAVLSIVAGVSIARLGGYAGAERPIIRVIPNTLTDTGLGYSGAALNGFADKAQVDDFLNAFGKVLYLEEAQIDIFTGYGVAGPNYVYYFIESLADAGVLAGLPREQAWQVALENVEGAVAMLRHSGKHPRQLLDINNSPGGVGIHALYELNNSDFAAGLQRSVKAAVKRTTELGQVHP
>NZ_LN831776.1|WP_020429787.1|1504591_1505422_+|hypothetical-protein
MKIRTLAAAALVGMSVVLGACGNKEAAGADKKDIVVGFGVGTYEEQFRLGIVPILEKEGYKVMIKTFSQNMQVNPAMKEGSIDASIFQSTAYMEGINKEIGADMAVLNFVPSAPQGLYSEKHKSLDEVKDGSVIAIPNDPVNQERAVRILEELGWVKVKPGAGTTDFNLSSVEPDKYQLKLEALDSAQILVSLADVDYGVVNGNYIANAKRQITEALKIENTPEQHRVTVTVNKDDLDTQWAKDLKAAYESKEFEEYIHAQDKYDGFILPDAWANN
>NZ_LN831776.1|WP_039789524.1|1503524_1504262_-|glycerophosphodiester-phosphodiesterase
MNNTINFAHRGASAVCPENTMAAFRKGLELGATGIETDVQMTLDGRLILIHDESLNRTTNRSGLVKDMTLSEVLKADAGSWFGAEFAGERIPVLEELLDLLQGRDTILNIELKNGTYLYPGMEEKVIAAVREYGMSERIVLSSFNHYSLAYCKSLAPEIRTGILYGEGLYRPWDYAASLQADALHAYHLAVLPEFVAGAAEHGVVYHPWTVNDPERMKYLIEAGVAGIITDVPDVLAGLLASRGV
>NZ_LN831776.1|WP_046501557.1|1502263_1503520_-|SLC45-family-MFS-transporter
MKKVWLLGFGFFSISITWSLYNAFVPFFLEKYVHSVALISFMMTIDNYFALFLQPWIGNRSDRTATRFGRRMPYLMIGMPLAAVLTMLIPFHSGLFTLLLFMMLMNLAMSLYRSPTVALMPDITPEHQRTKANGLINFMGGAGSILAFGAGSYLYDSSPVLPFVAAGLITLLCLFIVSRFIKEGRDGVNTAAANAPAGPAADRALQPGELVLPLSRPARVSLKKQLDRTTVWLLAAIFFWFVAYQGVETLFTLYGKHHLGLSEQAASFSLTFFSLAFVIFAIPSGWLGGRFGKKPVIILGVCGLMAVFALVGFAENVLLLRGLLLLGGIFWACININSYPFVVATGNEESIGTRTGIYYLVSSLAAITSPPLLGLLIDLTDYSTLFYAATASMAFALVCLLLMKGRARAVNTVHSNKA
>NZ_LN831776.1|WP_020429782.1|1501330_1502239_+|GGDEF-domain-containing-protein
MEARNYMLALSSVLIAALTIYSIYYLSPKFGGKHQKARAIRAVFMILIAGAGLSVMHLLGMQTLSEYAPDSESLFLPLTLYVLTLAGMLFLFSRLRQLLAEREQLKELAYRDSLTGLLNKNGMDHFWDHCKPNEQLAVLFLDLNRFKAINDTLGHHVGDLLLKAVGTTLSQFSSKGKRHIFRIGGDEFVIIAKRCSRKDAEQLALRILEKTTRNYKLEKHELFVSASIGITMSHGRIDRQKLLKEADSAMYNAKQLGSGRYSLHKQGQSASPSNPAGGSASLLHSSASSTNRLGDKQNSMRA
>NZ_LN831776.1|WP_046501550.1|1499564_1500842_+|IS91-family-transposase
MKNQETWKKRGIIRQILKDHFHGFMEMHGHHLPKGLHSSITETVNKAIRCGTRDMGYARYECKGCTKGAPEPVFICFTCKSRFCHGCGKKYTDEWAEKQQERILNVPHRHMVFTVPQELRKVFFQDRHKLNELSKQVAKVIQYYYRRKNKSKKYEVGVITVIHTFGRDLKFNPHIHTLITEGALEQNKEWKKVEYISYEYLRKAWQKLLLDLMMKWYPKEEWIKGLVNELYQRYPQGFYVNAEQRMKDARGASKYIGRYLARPAIAEYRVVSYDYHKVHYWYKDHRTGKRVDVVSPVMKFIYDLVQHIPPKHFRMVGRYGLYSRGKNKESQKVINLWRFMVHKQIEMTFPAEERKKKSYRQRMLESYGRDPMRCPCCKHRMLLVVIWHAEYGRIYYYDEEREYANQKKWGMRKGGKSTRTKERTG
>NZ_LN831776.1|WP_046501545.1|1498761_1499061_+|hypothetical-protein
MHRAVRAELRAAGMKALRAERLAVGGRIKGRNTFELARLAVGGRIKGKNTFELARLAVGGRIKGKNTFELARLAYRLATEIKDANPSIHRTDFLDQLLV
>NZ_LN831776.1|WP_020425919.1|1498171_1498756_+|histidine-phosphatase-family-protein
MTTIGLIRHGSTAWNKEGRIQGHTDNPLDEEGLQQAAAIAERLSGEQWDYIYSSDLLRAVQTAEVISKRLGIPIAGQVPGVREMNGGLIEGTTEDERVQRWGSGWKSMDMGLESDESGQQRGSRAIEEIAARHPGKRILIVSHGAILRSSLRKLVPGLDVGELLKNTSITHIVKDNSGWTCALYNCVAHMEAER
>NZ_LN831776.1|WP_020429794.1|1508190_1509879_-|alpha-glucosidase
MNKQWWKESVVYQIYPRSFQDSNGDGIGDLQGIISRLDYLEQLGINVVWLCPVYQSPNDDNGYDISNYQSIMNDFGTLADWEELLAGLHARGMKLIMDLVVNHSSDEHAWFAESRKSPDSPYRDYYIWRAGKDGHEPNNWGSFFSGPAWEYDAQTDEYFLHLFSRKQPDLNWDNPKLRREIYDMMTWWLDKGIDGFRMDVINLISKVPELPSVVKDQEDGERSYHFGGEYFVNGPRVHEYMQEMNREVLSKYDIMTVGEAIGVTPEEAALYVGEDRNELHMLFHFELMEVDSGPRGKWDVRPWKLADIKSIFSKWQTALHGKGWNSLYLNNHDQPRMLSRFGDDKHYPKESAKMLATLLHTLQGTPYIYQGEEIGMTNVKFDSISEYKDIEILNMYKEYRAAGHAEEEIMNSIYIKGRDNGRTPMQWSAEPQAGFTTGTPWLAVNPNYTEINVEQALADPDSIFHYYKKLIELRKSHDIFVYGDYAILAEEHEQVYAYLRTLGEERLLVMLNFFGRPAAFELPACVVFQDKTLVIANYGVQPEEDIRSLSLRPYEARVYRLR
>NZ_LN831776.1|WP_039789526.1|1509921_1510740_-|carbohydrate-ABC-transporter-permease
MKKTTNWPVTVIIALCSLLILFPLYMTIAIALKNPEEMARSIFSLPTGLHFENFANAIKATNFFNALGNSATITVTAVIFILLTNSMVAYAIARNMNKRFFKTLYFYFISAMFIPFQIIMLPVVKVTTDLHMNNIPGLIILYIVYGLAFNVFVYVGYIRSIPYELEEAATVDGASTWGTFWRIIFPLLAPVNATIGILSCLSTWNDFMLPLILLGNQDSYTLPLVQYVFQGQFSTDFNLAFASYLLALSPMLIIYLFAQKWIIGGLTQGSIK
>NZ_LN831776.1|WP_046501561.1|1510739_1511606_-|sugar-ABC-transporter-permease
MAKRRAAFYLMTIPALLLFFAFHTFPALQGIYYAFTNWDGYSNSFDYVGFKNFINIFKDENVLNSYLFTFKYAIATTVLINIISLLIALGLNAKIKAKNFFRGVYFLPNILSVLIVGFIFNYLFSNVFPVWGEKLGSDFLSQNILGNSDWAWIGIVIVAVWQGIAYNTILYLAGLQTIPHDLYEASNLDGASRWREFWSITFPLLASFFTINMVLAMKGGLMVFDQIIALTGGGPGRSTQSIALLIYTGGFQGGEFAYQSANAVIYFIVIVVISALQLKFLQKREMDL
>NZ_LN831776.1|WP_020429800.1|1511697_1512960_-|extracellular-solute-binding-protein
MKKTMKPVTVSLLAMSLLSACGNNSGSNAATDDGGNAASGEKVKIEFFQNKTEAKATFDKLVAQFNAANPDIVVSQINPPDAETVLKTRAAKQDLPDVIGLGATDTYKTLSASGLFEDFTGDPLVSSIQPAYVKMLNDLTGSSELNGIPFSANASGVIYNKAMFKEADVAVPTTWDEFIAAAQKFKDSGKYAFYLTLKDSWTSLTPFNSLEPSILGTDFFKKRTEGSVTFSDSFREIAEKQLKLTEFAQKDIFGKGYNDGNTAFAKGESAMYLQGVWAIPEIMKANPSLELGVFPFPATNDPAKNKVISGVDTLLTISKDSKHKEEAKKFVEFLLQPENVTAYITEQKAFPAVKGVTQNDPSTDGFKEAFTSGNLADFADHYIPGAMKVDTIIQSFLNKKDIDAYLKQLDTEWDKVANRK
>NZ_LN831776.1|WP_020429802.1|1513161_1514166_-|substrate-binding-domain-containing-protein
MNPTIKDVAQKANVSIATVSRVLNNLTGYSDKTKQKVNQAIKELGYQPNAIARGLINKRTQTIGVMFPKVSSAFSSDLLHGIDEFAHDSNYSVVVCNTDNDGKRTMKYLQLLREKQVDGIIFSSEVLSKEYYEVLESMKIPVVLVSSQTDFAKVPYVKVDDYQAVYDAIQFLISKGHRKIAMISGTKGDPIAGTPRVQGYRKALEANGIAFDSSRLVYGDFSFESGSRAMEALLRKAGEVTAVFAASDEMAIGALSSALKHGLNVPEDISIMGYDDLKPAQMVTPPLTTVRQPLYEMGKIASEKLIGMIETGEIAANRIMAHSIVERQTVRTLA
>NZ_LN831776.1|WP_020429804.1|1514713_1515661_+|AraC-family-transcriptional-regulator
MSIYLELPDVDKHFPFRSLICGGDELCYPHWHKEIEIIYVTKGRLNLGINDTPIRMEQGEVQFINGGDVHYFLASPESERVVIQFDLNLFQEVAALGSSGYSLRDLFTEMEHSSPSWPEAATAKVISLIESIYEEDTQRREGYAYLIKARMFELLTVILREIPKNRTQRQPKFSEDTLTQSRETMERLERIFAYVELHYQKSISLNEVARYMGFSPYYFTKLFKRNTGMTFVAFLNEYRLNKAKWILLNEDLPMSAVAEAAGFGSVKTFHHFFKEATGISPLKYHKTIFRNNTARMQEESAGADLYDRDIKTSGG
>NZ_LN831776.1|WP_020429805.1|1515668_1516745_+|Gfo/Idh/MocA-family-oxidoreductase
MTLKIGIIGCGGIANGKHMPALQKVEGAVMVAFCDIVPERAEKAKAEFGNESAAVYNDYKELLKDASIDVIHVCTPNISHAEISIAAMEAGKHVMCEKPMAKTTAEAQAMIDASVRTGKKLTIGYQNRFRADSAYLHTVCENNGLGEIYYARAKAIRRRAVPTWGVFLDEEAQGGGPLIDIGTHALDLTLWMMDNYKPKYAVGNAYHKLSGRKNAANAWGPWDPEKFTVEDSAIGFITMENGATIVLEASWALNTLDVGEARTVLCGTEGGADMEKGLRINGEEYGKTYEKHIGLDAAGVDFYDGAGDDPAVAEAKQWIESIVNNTEPVVKPEQALVVTRILEAIYKSSETGMPVFFD
>NZ_LN831776.1|WP_039789535.1|1517120_1517852_+|glutamine-amidotransferase
MTRVTVWNEYRHERQEERIREVYPQGIHAQLASFLSEAGLDTATATLDEPEHGLTEEVLNNTDVLVWWGHVAHQEVSDEIVNRVHQRVLQGMGLVVLHSGHMSKIFMKLMGTSCDLKWREAGEKERLWVMDPSHPIAEGIGEYIDLEQEEMYGAHFDVPAPESLIFVGWFEGGNVFPSGSTYRRGSGKIFYFQPGHESYPTYYNKEIQQVIINGVNWCAPAKRDYPVYGHSEALEPIREKVGV
>NZ_LN831776.1|WP_020429809.1|1517852_1518821_+|sugar-phosphate-isomerase/epimerase
MKLGVFDPVFGSLSLDEMLDKIAAAGLNAVEIGSGGNPGNPHCPTDELLASEAARKAYLEKFTKRGIMISAFSCHNNPISPDQEEARQGDEILRKSIKLASLMGVAVVNTFSGTAGDSDEAKAPNWPVTPWPTVYSDILTWQWEHKLIPYWKEIAQLAEEHGVKIGIELHGGFLCHTPYTILKLREATGPAIGANLDPSHLWWQGIDPVGAIKILGKAGAIHHFHAKDTYLDQDNINMYGLTDMQPYGDVQTRAWTFRSVGCGHSLSEWSNIMSALRTYGYDYVVSIEHEDPLMSVDEGFYRAVTNLQSILIREQPLDMWWA
>NZ_LN831776.1|WP_020429811.1|1519337_1519847_-|GNAT-family-N-acetyltransferase
MNHEITIKRLEELQPEIIQQLNTLIIDVVADGASIGFLSPLAAEEAEAYWRGVLAPGVLLWVAQEGDSIVGTVQLHPESKPNSPHRAEIAKLMVHPEHRRKGIARMLMETAEQAAVAGGRTLLVLDTREGDPSNLLYQSRGFVEVGKIPDYVINSDGEMSATVIYYKHQ

Crispr_ID: NZ_LN831776_20

• CRISPR_ID: NZ_LN831776_20
• CRISPR_location: 1558481-1558554
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_20

Consensus_repeat	Method
AATTAGTGACCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_20

>20.1|1558504|28|NZ_LN831776|CRISPRCasFinder
AACCTGCGAAGAATAGGGTGTTCAGGTA

CRISPR arrays and Neighbor proteins around NZ_LN831776_20

CRISPR arrays

The CRISPR arrays of NZ_LN831776_20

>merge|NZ_LN831776|20|1558481-1558554|CRISPRCasFinder
AATTAGTGACCCTTTTTCCACTTAACCTGCGAAGAATAGGGTGTTCAGGTAAATTAGTGACCCTTTTTCCACTT

>NZ_LN831776|20|20|1558481-1558554|CRISPRCasFinder
AATTAGTGACCCTTTTTCCACTT	AACCTGCGAAGAATAGGGTGTTCAGGTA
AATTAGTGACCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020427627.1|1566963_1568145_+|alanine-racemase	unknown	unknown	gnl|CDD|143481
NZ_LN831776.1|WP_020427641.1|1553071_1554352_+|B12-binding-domain-containing-radical-SAM-protein	unknown	unknown	gnl|CDD|223963
NZ_LN831776.1|WP_081487155.1|1562585_1562915_+|DUF4367-domain-containing-protein	unknown	unknown	gnl|CDD|379540
NZ_LN831776.1|WP_020427632.1|1561184_1562417_+|MFS-transporter	unknown	unknown	gnl|CDD|340882
NZ_LN831776.1|WP_020427635.1|1559289_1560048_+|DUF3600-domain-containing-protein	unknown	unknown	gnl|CDD|289015
NZ_LN831776.1|WP_020427636.1|1558715_1559300_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|183582
NZ_LN831776.1|WP_020427639.1|1555196_1556330_-|copper-amine-oxidase-N-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|377924
NZ_LN831776.1|WP_020427637.1|1557478_1558150_+|O-methyltransferase	unknown	unknown	gnl|CDD|226607
NZ_LN831776.1|WP_020427628.1|1565654_1566740_+|outer-membrane-lipoprotein-carrier-protein-LolA	unknown	unknown	gnl|CDD|225390
NZ_LN831776.1|WP_020427634.1|1560215_1560395_+|aspartyl-phosphate-phosphatase-Spo0E-family-protein	unknown	unknown	gnl|CDD|378175
NZ_LN831776.1|WP_020427644.1|1549555_1550710_+|winged-helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|294013
NZ_LN831776.1|WP_020427640.1|1554412_1555192_-|TatD-family-hydrolase	unknown	unknown	gnl|CDD|238635
NZ_LN831776.1|WP_020427630.1|1562971_1565029_-|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|223910
NZ_LN831776.1|WP_052741420.1|1541707_1547593_+|hypothetical-protein	unknown	unknown	gnl|CDD|377038
NZ_LN831776.1|WP_167345588.1|1562428_1562605_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427642.1|1552448_1553033_+|histidine-phosphatase-family-protein	unknown	unknown	gnl|CDD|366010
NZ_LN831776.1|WP_020427633.1|1560368_1560944_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|379883
NZ_LN831776.1|WP_039787249.1|1556459_1557356_-|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223656
NZ_LN831776.1|WP_046501584.1|1550795_1552070_+|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_LN831776.1|WP_020427645.1|1548763_1549510_+|YjgB-family-protein	unknown	unknown	gnl|CDD|372945

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020427627.1|1566963_1568145_+|alanine-racemase	gnl|CDD|143481	cd00430, PLPDE_III_AR, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzyme Alanine Racemase. This family includes predominantly bacterial alanine racemases (AR), some serine racemases (SerRac), and putative bifunctional enzymes containing N-terminal UDP-N-acetylmuramoyl-tripeptide:D-alanyl-D-alanine ligase (murF) and C-terminal AR domains. These proteins are fold type III PLP-dependent enzymes that play essential roles in peptidoglycan biosynthesis. AR catalyzes the interconversion between L- and D-alanine, which is an essential component of the peptidoglycan layer of bacterial cell walls. SerRac converts L-serine into its D-enantiomer (D-serine) for peptidoglycan synthesis. murF catalyzes the addition of D-Ala-D-Ala to UDPMurNAc-tripeptide, the final step in the synthesis of the cytoplasmic precursor of bacterial cell wall peptidoglycan. Members of this family contain an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain. They exist as homodimers with active sites that lie at the interface between the TIM barrel domain of one subunit and the beta-sandwich domain of the other subunit. AR and other members of this family require dimer formation and the presence of the PLP cofactor for catalytic activity. Fungal ARs and eukaryotic serine racemases, which are fold types I and II PLP-dependent enzymes respectively, are excluded from this family.	4.62613e-176
NZ_LN831776.1|WP_020427641.1|1553071_1554352_+|B12-binding-domain-containing-radical-SAM-protein	gnl|CDD|223963	COG1032, COG1032, Fe-S oxidoreductase [Energy production and conversion].	2.47618e-40
NZ_LN831776.1|WP_081487155.1|1562585_1562915_+|DUF4367-domain-containing-protein	gnl|CDD|379540	pfam14285, DUF4367, Domain of unknown function (DUF4367). This family of proteins is found in bacteria, archaea and eukaryotes. Proteins in this family are typically between 229 and 435 amino acids in length.	1.73834e-08
NZ_LN831776.1|WP_020427632.1|1561184_1562417_+|MFS-transporter	gnl|CDD|340882	cd17324, MFS_NepI_like, Purine ribonucleoside efflux pump NepI and similar transporters of the Major Facilitator Superfamily. This family is composed of purine efflux pumps such as Escherichia coli NepI and Bacillus subtilis PbuE, sugar efflux transporters such as Corynebacterium glutamicum arabinose efflux permease, multidrug resistance (MDR) transporters such as Streptomyces lividans chloramphenicol resistance protein (CmlR), and similar proteins. NepI and PbuE are involved in the efflux of purine ribonucleosides such as guanosine, adenosine and inosine, as well as purine bases like guanine, adenine, and hypoxanthine, and purine base analogs. They play a role in the maintenance of cellular purine base pools, as well as in protecting the cells and conferring resistance against toxic purine base analogs such as 6-mercaptopurine. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. The NepI-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.4634e-67
NZ_LN831776.1|WP_020427635.1|1559289_1560048_+|DUF3600-domain-containing-protein	gnl|CDD|289015	pfam12207, DUF3600, Domain of unknown function (DUF3600). This family of proteins is found in bacteria. Proteins in this family are approximately 230 amino acids in length. This domain is the C terminal of the putative ecf-type sigma factor negative effector.	9.89562e-11
NZ_LN831776.1|WP_020427636.1|1558715_1559300_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|183582	PRK12543, PRK12543, RNA polymerase sigma factor; Provisional.	1.19186e-58
NZ_LN831776.1|WP_020427639.1|1555196_1556330_-|copper-amine-oxidase-N-terminal-domain-containing-protein	gnl|CDD|377924	pfam07833, Cu_amine_oxidN1, Copper amine oxidase N-terminal domain. Copper amine oxidases catalyze the oxidative deamination of primary amines to the corresponding aldehydes, while reducing molecular oxygen to hydrogen peroxide. These enzymes are dimers of identical subunits, each comprising four domains. The N-terminal domain, which is absent in some amine oxidases, consists of a five-stranded antiparallel beta sheet twisted around an alpha helix. The D1 domains from the two subunits comprise the 'stalk' of the mushroom-shaped dimer, and interact with each other but do not pack tightly against each other.	3.55272e-08
NZ_LN831776.1|WP_020427637.1|1557478_1558150_+|O-methyltransferase	gnl|CDD|226607	COG4122, COG4122, Predicted O-methyltransferase [General function prediction only].	5.58082e-56
NZ_LN831776.1|WP_020427628.1|1565654_1566740_+|outer-membrane-lipoprotein-carrier-protein-LolA	gnl|CDD|225390	COG2834, LolA, Outer membrane lipoprotein-sorting protein [Cell envelope biogenesis, outer membrane].	5.14762e-24
NZ_LN831776.1|WP_020427634.1|1560215_1560395_+|aspartyl-phosphate-phosphatase-Spo0E-family-protein	gnl|CDD|378175	pfam09388, SpoOE-like, Spo0E like sporulation regulatory protein. Spore formation is an extreme response to starvation and can also be a component of disease transmission. Sporulation is controlled by an expanded two-component system where starvation signals result in sensor kinase activation and phosphorylation of the master sporulation response regulator Spo0A. Phosphatases such as Spo0E dephosphorylate Spo0A thereby inhibiting sporulation. This is a family of Spo0E-like phosphatases. The structure of a Bacillus anthracis member of this family has revealed an anti-parallel alpha-helical structure.	8.31708e-07
NZ_LN831776.1|WP_020427644.1|1549555_1550710_+|winged-helix-turn-helix-transcriptional-regulator	gnl|CDD|294013	cd00383, trans_reg_C, DNA-binding effector domain of two-component system response regulators. Bacteria and some eukaryotes use two-component signal transduction systems to detect and respond to changes in the environment. The systems consists of a sensor histidine kinase and a response regulator. The former autophosphorylates a histidine residue on detecting an external stimulus. The phosphate is then transferred to an invariant aspartate residue in a highly conserved receiver domain of the response regulator. Phosphorylation activates a variable effector domain of the response regulator, which triggers the cellular response. This C-terminal effector domain belongs to the winged helix-turn-helix family of transcriptional regulators and contains DNA and RNA polymerase binding sites. Several dimers or monomers bind head to tail to small tandem repeats upstream of the genes. The RNA polymerase binding sites interact with the alpha or sigma subunit of RNA polymerase.	1.53892e-26
NZ_LN831776.1|WP_020427640.1|1554412_1555192_-|TatD-family-hydrolase	gnl|CDD|238635	cd01310, TatD_DNAse, TatD like proteins; E.coli TatD is a cytoplasmic protein, shown to have magnesium dependent DNase activity.	2.55317e-53
NZ_LN831776.1|WP_020427630.1|1562971_1565029_-|HAMP-domain-containing-protein	gnl|CDD|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	1.09781e-53
NZ_LN831776.1|WP_052741420.1|1541707_1547593_+|hypothetical-protein	gnl|CDD|377038	pfam03442, CBM_X2, Carbohydrate binding domain X2. This domain binds to cellulose and to bacterial cell walls. It is found in glycosyl hydrolases and in scaffolding proteins of cellulosomes (multiprotein glycosyl hydrolase complexes). In the cellulosome it may aid cellulose degradation by anchoring the cellulosome to the bacterial cell wall and by binding it to its substrate. This domain has an Ig-like fold.	1.06716e-28
NZ_LN831776.1|WP_020427642.1|1552448_1553033_+|histidine-phosphatase-family-protein	gnl|CDD|366010	pfam00300, His_Phos_1, Histidine phosphatase superfamily (branch 1). The histidine phosphatase superfamily is so named because catalysis centers on a conserved His residue that is transiently phosphorylated during the catalytic cycle. Other conserved residues contribute to a 'phosphate pocket' and interact with the phospho group of substrate before, during and after its transfer to the His residue. Structure and sequence analyses show that different families contribute different additional residues to the 'phosphate pocket' and, more surprisingly, differ in the position, in sequence and in three dimensions, of a catalytically essential acidic residue. The superfamily may be divided into two main branches. The larger branch 1 contains a wide variety of catalytic functions, the best known being fructose 2,6-bisphosphatase (found in a bifunctional protein with 2-phosphofructokinase) and cofactor-dependent phosphoglycerate mutase. The latter is an unusual example of a mutase activity in the superfamily: the vast majority of members appear to be phosphatases. The bacterial regulatory protein phosphatase SixA is also in branch 1 and has a minimal, and possible ancestral-like structure, lacking the large domain insertions that contribute to binding of small molecules in branch 1 members.	3.21334e-34
NZ_LN831776.1|WP_020427633.1|1560368_1560944_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|379883	pfam16859, TetR_C_11, Bacterial transcriptional repressor C-terminal. This family of bacterial transcriptional repressors is characterized by the short approximately 50 amino acid stretch of residues constituting the helix-turn-helix DNA binding motif, around the YRFhY motif. The target proteins that are repressed are involved in the transcriptional control of multi-drug efflux pumps, pathways for the biosynthesis of antibiotics, response to osmotic stress and toxic chemicals, control of catabolic pathways, differentiation processes, and pathogenicity. Another target protein is BetI, an osmoprotectant which controls the choline-glycine betaine pathway in E.coli.	2.42145e-29
NZ_LN831776.1|WP_039787249.1|1556459_1557356_-|LysR-family-transcriptional-regulator	gnl|CDD|223656	COG0583, LysR, Transcriptional regulator [Transcription].	3.00304e-53
NZ_LN831776.1|WP_046501584.1|1550795_1552070_+|MFS-transporter	gnl|CDD|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.80538e-46
NZ_LN831776.1|WP_020427645.1|1548763_1549510_+|YjgB-family-protein	gnl|CDD|372945	pfam14172, DUF4309, Domain of unknown function (DUF4309). This family includes the B. subtilis YjgB protein, which is functionally uncharacterized. This is not a homolog of E. coli YjgB. Expression of B. subtilis YjgB is regulated by the alternative transcription factor sigma-B. This family is found in bacteria, and is approximately 140 amino acids in length.	6.47437e-55

Protein sequences

>NZ_LN831776.1|WP_020427637.1|1557478_1558150_+|O-methyltransferase
MGEMNTWSEVDGYFNSRLLPADPVLDTVLDANAGAGLPAIDVAPNQGKLLYLLAKMKGAANILEIGTLGGYSTIWLARALPEAGRLVSLEYEHKHVVVALDNLRLAGLADKTEIIEGPALESLAALEARGAAPFDFIFIDADKPNNPHYLKWALKLACPGAVIVADNVVRGGEVVQADSKDDRVQGIRQFIDLLAAEPRVEATALQTVGSKGYDGFVLGVISG
>NZ_LN831776.1|WP_039787249.1|1556459_1557356_-|LysR-family-transcriptional-regulator
MNIHALRLFYYVAETGSVTKAAARLNISQPAVTSQIKKFEKDLGLPLFNPSGRGVSLTPFGIELAKQAGNFFTYEEQIDEFVEDYRHGRKGKLRIAATYLPANFLVPGWAARFKAGYPEIEMEITTTNSQQAFEQLKRHEADVAFYGGGAQDRPEDIDWLELFEDELWFVVSPSHPYAGRTVSLQEMMLEPFIMREEGSSTRARLVSLCVTYGLKPPQVTLQFSGLGEAIRSVMAGYGANFISSLAVREYVEQKRLSRVQVEGIQLSNHIAICTRSHESVPPALQQFIDICRSFPPEL
>NZ_LN831776.1|WP_020427639.1|1555196_1556330_-|copper-amine-oxidase-N-terminal-domain-containing-protein
MKKILTASALALLIAGCAAAPTIDSVSAAAPLTLSVDGQSVLPKLRPFYSGELLYVPARALLEYYPVELKWDNAHKKLSLTTNSSRSVLSPGSSAMQVQYTQTDGGYVDKLEGPVLLKEGHVYVSAGTVSLLTGAEAKPAASGNTVSITSGDVSTSVRVLKEPLAIAAGSSGKAKLYTARKQGSTYKGFMLEVNGRKHSFNWESPRLVSYPPELHYADVDDDGKPEAIVILSLGTGTGISQEELHVVKPEVWKELAVPTAEKAASAAVSSRITLDNSDVVVRLELAGAAPSKVTLRLPGRAGDGGLDHFGTEAGIGAVTHYKVVNGKLKAETSVNAGIGESMGTLMLDYKAGNGGMVLDTIRFQPHDTTEQYVEKEQ
>NZ_LN831776.1|WP_020427640.1|1554412_1555192_-|TatD-family-hydrolase
MIDAHIHLEQYEDSELQAMLPGLLEQDIQSLVAVSMNLDSCIRTQEIAARYPGRVKPAYGFHPEQPAPTESELAALLKWISQHAGEMVAVGEIGLPYYSRAEALARGEAFEQEPYLRVLDNLLALAARLNKPVVLHAVYEDAITACNLLEKHGIARAHFHWFKGPEEAVTRMIERGYHISFTPDIVYEPEIRELARRYPPGLVMAETDGPWPFEGPFAGRPTRPAMVHDVAAAWAELHGYSAAQAKAMLTANTARFYQL
>NZ_LN831776.1|WP_020427641.1|1553071_1554352_+|B12-binding-domain-containing-radical-SAM-protein
MKKSILLIQPENQKINSFRRKQFNNFVQITMPYLAGFIDEAKYKITLVDEYQQQIPYTRKFDLVAITVNTPNSGHCYKMAEKFQAAGAKVVMGGPHATLLPAEVSEHCDIIVIGEAEATWPQLLEDFYQGKYQTEYRSDAIPELTNLPLPRWDLLHRNPLMKGAVISTRGCPYNCSYCNLKQIYHNRFRTRPVSEVIHEISLMKSRFFVFWDDNFFADKAHAIEVMEQLRPLRKKWAAQVTLADCNNDELLEKASAAGCLYLFVGLESFSPAALRGVNKGMNRVDAYRDIIGKLHRHNIMIQAGIVFGFDEDTPDSFRQTLEGCEALGIDGVTVSLLTPLPRTPIYARMKREQRLLHEDWSLYNGKTDVVFHPAGMTSEQLYEGYLDFRRRFYSLPSFIRRMRVSGTHPVYNFVMNLGYRLAIKRG
>NZ_LN831776.1|WP_020427642.1|1552448_1553033_+|histidine-phosphatase-family-protein
MTTTTYIYMVRHGDSLKTSGNERSRFLSAQGEKDAQRVTQRLLGEGIDALYSSPYTRAVDTIAGLAGALGKEIHKVEDLKEKCWTEDDRTLQDPELYPFLEQMFAEPDFVLEDGGESNRVCKERAVKALKEILRNHPGERIVIGTHGMVMTLMMNEFAEEYGLDFLLQTRKPDIYRMEMKDGLLSHVQRMPLDD
>NZ_LN831776.1|WP_046501584.1|1550795_1552070_+|MFS-transporter
MEASVKQGNSLLHNKVYMRVYSAYATAAFGDWFDSLAIQVLVGYRWHASPLMLALIPVAVALPSVLLGSVAGVAADRLNKLKLMRMCDLLTAFLTVLVLFAPNMVWLLPLLALRSALSTLNVPAQQSMTRSIVREDQLLQATSLNGIVNQGSKIAGPLLGGVALTLLSPQWCILLNAIFRVGSYLLLLSVKNIHTGDEHPAAEVQEERVPLRKMWAEGWSFMLRSRLLLHTMLFGLTGALAIQIIDFQFTSLFRVISPANESLLGWMVAASGVGAVSVILLLGKLKPGTSYGLRLGMGYVLIGGSVGGLGLLQPGASVIWVLLFGLILGLGNGSFFVAFNYCLQKETPPHMTGRIFGIQSSILGLVMITAPLLGGWLVQVAGPGRIFMNFGMVQVLLGLVGVLFGRVLWPEAKRESVQPMVEHS
>NZ_LN831776.1|WP_020427644.1|1549555_1550710_+|winged-helix-turn-helix-transcriptional-regulator
MHLELNNSEYKVMADGITITLLPKEFALLQFLYRNVGRTFSREQLLDHVWPLEYPVERTVDDHIYRLRKKLHVLSGLDIKTVRGFGYSLAVPGTPAGVALNPAMNDPELRETMRSVFSKFHVYGQGKSMVTLARQQDILGYELDSVYSMVIHFVQGDLEWLLHTDEVPLKERLFYLMIFYFLSGDPKERLAYCEQVIELKLVYPNYQLELEILTILDLFTLAGQPERALERLKRSHQVIAELGYDNFIPVTLITELFVHLTAGTGDEELKRMDEAIGVILQEKPFLREIGSYKVVKGLWSLRLEQWREAENLLSEGLQVLEMSGFIPLRLYSLYRIVHFCRMFPPPKALQHKYEEIFVAELEQSGLNRFSQSLEDTMQQVLKSL
>NZ_LN831776.1|WP_020427645.1|1548763_1549510_+|YjgB-family-protein
MTNSLKTITGILILAGMLGLTGCSSGSNNEATASPAALQPGASSSGSNDAATASPAAASATEAPTAPQPGASSSSAPSAAPAEASATASPSAPGGGASSAAAPQDSSKLLEELLQLAREGKVPGVEYAAHTGLIDDVEAAWGEPDTKETAGKGIYATYSKQHVVIGFNKGSRIFDVRSSAADLQKLTLKEIEAVLGEPEKTAVNGGDKIYMYQAGKQYELKFIIPEASGTVDHISVFSEQDSINNMAG
>NZ_LN831776.1|WP_052741420.1|1541707_1547593_+|hypothetical-protein
MKRSFKHSRHSLIGMFLLGIAVFFCLRPADLYAAGPTPDSFTTTSYSSLPSNAMSAMAYGNNVYIAVGYYGAIIKSADAETWVNVKTKADINYTGVTAPGSFTFNGAAYGNGLFVVTGSEGVILTSPDGNTWTQRSSGVTSGIWSTEFLTFNGSSAFYATTQGKLLTSPDGINWTSIVPTGVDSSLTLTKVTVGNGGTRLAVGGANGRIYSTTNGTAWTSAQPSTAEGQSIGTNMVTWMNDRYYISDPRAYIWTSTDLSTFTLLGPPFKQNASQHNNQMFNGFYDGTKYYMFGYESPNYGAVYTSTNGTTWTMQPFKNYFVTQNARYLNGKYFRLGNEGMLVSSDGADWRYKWGGAFTEIVHGSGSQYVAVGKTGGDGAIWNSADLAHWNEVTLSPRTTGFNAAAYGNNTYVAVGETNQTTTALATSPDGTTWTLRSGINDSTTLSDIAFGNGKFVAVGSGAGGPKIKTSEDGVSWHEPALPVQSIDAVYSIAYTNNQFIALGYGYSDEGYLNAASIWTSADGETWSNRSGAYPNQTDGFNNLLYDGSKYVLTGYDSSTYEVFSRSSEDLTTWSSPTLTGTYTYFSSSAMLGQKGNNLYMLAYDSSNTPVVYYTADHGSTWQNAGVDMSSIDPNAIYSLMEADEKVLLSGNSQLVMTTTGTLAQAEAPTANPAGGAVAPGTTVALSSATSGAAIHYTLDGSVPTSSSPVYSGPIPVTSAVTIKAIAVKAGMTDSAVMSEAYTIMAQVEAPTANPAGGAVAPGTTVALSSATSGAAIHYTLDGSVPTSSSPVYSGPIPVTSAVTIKAIAVKAGMTDSAVMSEAYTIMAQVEAPTANPAGGAVASGTTVALSSATSGAAIHYTLDGSVPTSSSPVYSGPIPVTGAVTIKAIAVKAGMTDSAVMSEAYTIMAQVEAPTANPAGGAVAPGTTVALSSATSGAAIHYTLDSSVPTSSSPVYSGPIPVTGAVTIKAIAVKAGMTDSAVVSEAYTIMAQVEAPIANPAGGAVAPGTTVVLSSATSGAVIHYTLDGSVPTSSSTEYSGPIPVTGSVTIKAIAVKAGMTDSAVVSEAYTIMAQVEAPTANPAGGAVAPGTTVTLSSATSGAAIHYTLDGSVPTSSSPVYSGPIPVTGSVTIKAIAVKAGMTDSAVVSEAYTIMAQVEAPTANPAGGAVAPGTTVTLSSATSGAAIHYTLDGSVPTSSSPVYSGPIPVTGAVTIKAIAVKAGMTDSAVMSEAYTLSTEPELDSIISPVSAAFDKKQTQQADVTIELTLNGNTLIGISNGIANLTAGTDYTLSGSTVTISKTYLASLAAGTTSLTFRFSAGAAQTLDITITDTTVPIPGVPLLQSAVFGNAQVQLIWTPVEGSTGYKIFQRLADTEYGSEIATVSGSVYSYNAVNLLNGTTYYFVVKAANAEGDSAASNELSATPKTAPGAPTNVTAVSGNGQAVVSFTAPDSDGGSPITGYEVISSPGNIVAYGTASPITVTGLTNGTAYTFTVKAINSAGSSTTSALSNTVTPIAPSSGGGDTPPSVPVAPATPATPAAPPPAVTGFNVLVNGKVENAGTITTATVNGQTALTVAIDQAKLEEKLAAEGQGAVVTIPVTVKSDIVIAELNGQMVKDMEDKQAVLELKSENATYTLPAGQINMDAIRSQFGTAAALGDIKVKLEIAAPAEDTLKTVENSAVQGGFTLVAPPLNFVVRAEYGGQTVEISKFSAYVERQIALPDGVDPNKITTAIVVEPNGSVRHVPTRVTTMDQKYYAKVNSLTNSTYSIIWHPLEFKDVAGHWAKDIVNNMGSRMIIDGTGNGLFDPDADITRAEFAAVIVRGLGLKLDSSAASFADVKAGAWYSSAVQTAYAYHLINGFEDGTFRPADKITREQAMAIIAKAMKLTSLKDKLPVQSSAELLSPFKDASKISQWAQSGAADSIEAGIVSGRSASELAPQAYITRAEVAAIVQRLLQKSNLI
>NZ_LN831776.1|WP_020427636.1|1558715_1559300_+|sigma-70-family-RNA-polymerase-sigma-factor
MEDQTEYSQLITRTLAGSREAYGELYEATIRDVYRTVHFLVSEPSDADDVVQDIYLELHRSLKQYNESRAFRPWLMGLVMRQVHAYRRKGWRQLRISKKAEHTSEIQDADVAGEVIDRLSSRMLMDKVNSLPYKLRQVIVLHYLQEYSQEEAAAILGIPLGTVKSRIHAALQKLRRKQKADTIRIGKVEDLHES
>NZ_LN831776.1|WP_020427635.1|1559289_1560048_+|DUF3600-domain-containing-protein
MSLEENLRRTLQAETEGWSAPPELKGKILDRIEPGKGGRRMKKWLIATILAASLVIPAGAYAGYHYLSDSMYGSQDNFVQNGGTLEQYEQVEAKLQQAKQSLSEEDFNTMISLLHKLGSFNLQIADASGMLHPEKLSAKDRERYNRLGAELEPYFSKLKNPKKPQQPVEQVDPDAFWDQQLAKAQKTFSGGELDEVQRLIGELKVLNAKVTDPDGSIHMDRLTQADQSSQDRLIEELNPYLKKLGVQLKPSS
>NZ_LN831776.1|WP_020427634.1|1560215_1560395_+|aspartyl-phosphate-phosphatase-Spo0E-family-protein
MNKLEAIQQRIEAERRKLNEMETTYGLLHPKVIRQSMKLDTLINEYTKELSLRSNPFES
>NZ_LN831776.1|WP_020427633.1|1560368_1560944_-|TetR/AcrR-family-transcriptional-regulator
MDKKRGRPRNNEAEAAILAASYDLLLETGFGAVTVEKIAERAKVSKATIYKWWPNKAAVVIDGYLSAATARLPVPDTGSVKEDIRIHATNLAAFLYSREGKVITEMIGEGQFDAGLAEAYRTRFFAPRRQEARQLLERGVMRGELKKDLDVNCSIDLMYGPIFYRLLITGDTLNGEFVEKLLALAFEGIRA
>NZ_LN831776.1|WP_020427632.1|1561184_1562417_+|MFS-transporter
MNQVNQASRGMNVKHAQASAASKAVPGWITFLLAASCGLIVANLYYAQTLVGPISAATHLSSGAAGLIVTLTQIGYVIGLLFVVPLSDIIENRRLTVTSLAVVVAALAAATLAPNAPLFLAASLFIGLGSVAAQILVPYASYLAAEEHRGRVVGNVMSGLLLGIMFARPLASFVSGLWGWHAIFAISAVIIALLTILLSRVLPKRQPIPTMNYGGLIRSLGTLLKTTPVLRRRALYQASLFGTFSLFWTTVSLRLADTYHLSQQGIALFALAGVAGAVAAPIAGRLADRGWTRPLTGLAFVLAAAAFLIAYLFQSDSKVTLGLLVVGAIILDMGVSGNLVLGQRAIYSLGNEARGRLNGLFMAIFFIGGAIGSSLGGWAYAYGGWGLTTLIGLALPVLAFLYYLTEKKQA
>NZ_LN831776.1|WP_167345588.1|1562428_1562605_+|hypothetical-protein
MLKRLLSGLDQPALESGLFFLYENTKQQKVQHNPHTAEKQTMILEGIRKICKAAEVST
>NZ_LN831776.1|WP_081487155.1|1562585_1562915_+|DUF4367-domain-containing-protein
MPKYLPEGFAFDHGEFSKGEQGVNGKYLDLIFTSEKIGQKLSMQFRYSDEETAYEMSTSGKMEKVQVNGADAVMMDDRSLHWEADGVLYAMNTCGLERSEVLKIAESIR
>NZ_LN831776.1|WP_020427630.1|1562971_1565029_-|HAMP-domain-containing-protein
MWKADNVSPKISNISLKVKLPVLLSLLVAVVLLATSVTVYLFSSDLLLRKSKDEINANSDRIGEGLWTAMQLEEQIAYVISVHNTFKELLELREQGTLSDQAFFSPDNPLFSKANTILQDSLQGGNDSLLVLDSQGTIVAGTNKESLGQSRVDREYFTEAFKGKSFISDAIVSKSNNKLLLVFSQPVKSADGKVLGVLAMTVASDFFLDKLGNININAKGKIEVLSRGGIVLYNSSDPARIGQDVGDDPGIKPLLETRATDELEIQTTELGTEYLRINKIPKADLTISVIDSYDDIERPIQDMLMKILIVTVIALLVAIGFGLLLSRSITKPVVTLTSRFKTLATGDLTVTADGSYKSEFKDLADSFNTMVQQNKALITNMNDSITILKTSTHELEETSKQAARSVNETSVTSMGIAQAMELQSNDTEQIVNKFYGFSEKFAGMNDNAQAVRQRAEEITQVFHTSNQVVEGLIEISSKNEQEVQKISAITVKLQDSSNSISNITGAINQIAAQTNLLALNASIEAARAGEHGRGFAVVASEIRKLAEQSSRQSNEIYEIIQQNLAFVAENNDSVMEINQISAQQDELVGQTQTAFQTILDKITEITVQIQSMADEIAHMQKDKDEVLDSAQSLSATGEEVSASVEEVTATMMEQSSAVDQLAEMVGTIDQLSKSLAEAASKFRIE
>NZ_LN831776.1|WP_020427628.1|1565654_1566740_+|outer-membrane-lipoprotein-carrier-protein-LolA
MRRITWVLAIIMSVALVLAGCGKKDAASVVKDLNNVSDKLESKQGAYQGSGTMTLYTGEQPQEYKVEVWYKNPSYYRISLSNVQKDVTQIVLRNDEGVFVLTPSLGKSFRFQSDWPDNQGQVYLYQTLLRGIVSDNNRQFAEDGDNYVFEVAANYQSSALVRQKIWLAKKTYEPKQVQVSDSEAKVVVNVKFDSFKFDPEFTKDSFDMQKNMATGSASESTLAEVDENGNPVAAPENARQEGQTAAAEPGDFGIIEPGYIPAGVQLKDSNKLEDSKDHSVLLRYDGTYQYTIIESRPLDRAVSLAPATLIDLGFTAGALTGDEQKTLTWMSDGVQYRITSANLPVNEMMQIAASMEEQSGK
>NZ_LN831776.1|WP_020427627.1|1566963_1568145_+|alanine-racemase
MQASYRPTVAEINLDDLRANYEAFRKALPAETKFMGCVKGNAYGHGAVEVTRELERLGADYVSVAFLDEALELRQAGILIPILVLGYTSPEGIPVAWKNHVTVTLFTPEVLEAVRQLPVDPEHRLKVHIKIDSGMGRLGLLPADAPDFIAEVHSVAQAELEGMFTHFAKADESNKSYTLMQYRRFMSVAETLRDRDIHIPIIHTGNSATAIDTPLLSSNMVRVGISLYGFYPSTEVNRELVALHPVMTLKTQAVYVKTLPPDWGISYGTRYFTDSEEIIATLPVGYADGYSRMLTGKAEVLIRGRRVPVVGTICMDQCMVTLKSFAEEAEQIKAGEEVVLIGRQGAVSITADELALHLGTIHYEVICMLAHRVPRVYVREGAAPNLVNPLLQT

Crispr_ID: NZ_LN831776_21

• CRISPR_ID: NZ_LN831776_21
• CRISPR_location: 1592755-1594917
• CRISPR_type: TypeIII
• Repeat_type: I-C
• Spacer_info: 32 spacers
• Cas_protein_info: cmr1gr7,cas10,cmr3gr5,cmr4gr7,cmr5gr11,cmr6gr7,PD-DExK,cas3,cas5,cas8c

Consensus repeat of NZ_LN831776_21

Consensus_repeat	Method
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	PILER-CR
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CRISPRCasFinder
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CRT

spacers of NZ_LN831776_21

>21.1|1592787|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
TTTTGGTTTTTAAAGATGGAAGAGTTGTAGAGAA
>21.2|1592853|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
AAGGCACAAGAGAGCAGCCGAGCTACAGAACGCC
>21.3|1592919|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
AGGGCCTTATCCATTATGACTACATCATATTTTC
>21.4|1592985|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ATGCTCTGTTTATCCTTGCTTCCGGGCCAAAAAT
>21.5|1593051|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CAATTGGCGGACGAACAGCAGTGGGGTTGGGTGG
>21.6|1593117|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CGAAACTGCCGGAAGTCGTGAAACAAATGTCCAAG
>21.7|1593184|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CCTAATCACTGCTACAAGCCGCGCAAGACTATGC
>21.8|1593250|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CGGGCGTTGTACCAGTCCAAGAAATCACCATGTAG
>21.9|1593317|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ATTTGAAGCTGCACAGGAAGCCGTCCGCAGGCTCTG
>21.10|1593385|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ATATGGAGCAATCAAGCCTTTATCAAAATCACGAAA
>21.11|1593453|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ACTGAAACAGTCAAAGAACTCAAAGAGGCCGTCAAG
>21.12|1593521|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CTGGTAGTCCATTGTTCACTCCAGCGGGATTATC
>21.13|1593587|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CAGATCAATTTAACATCGTCCATACTCGCACGGT
>21.14|1593653|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
TATATACCGTGGATCATTATCGTGATGCTCATTTT
>21.15|1593720|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CATAAGATCATCCAGGATCTTGTCCTGCTTATTC
>21.16|1593786|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
TTGCTGACAAGTGGCGAGTCTGTCATCCGCAGCACA
>21.17|1593854|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
TGAATTCTTGCCGGATCTGATAAACCTCTTGTAT
>21.18|1593920|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
TATTTTCACCTCTGCGGTAATTGTGCCGATCCGGG
>21.19|1593987|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CCCATCGCCCTCGTTGATTAGTTTTTTACTTCA
>21.20|1594052|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CTCCGCGCTCATTACACTATTTAACTCATGTTGC
>21.21|1594118|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
AATGAGCATGACTGCCAATAGGCTGTTCACATAG
>21.22|1594184|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
GCCTTGTCCCTGCATTTTGGATTTTGGCACCAAT
>21.23|1594250|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CAACTACTACAAAACCCCACTCGAACAATGGATT
>21.24|1594316|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ACTCTCTAAAGCCTCGATGTGCCATTCCTGCAATC
>21.25|1594383|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CGGGTGATCGGAGGAGACGAATAATGGCAGTAGA
>21.26|1594449|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
TGCGACCTCTGACGCAAATGCAGCAGCCGGAGAAA
>21.27|1594516|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CGAATCATATTTTTAAGAATGATGGCGTGCTGCT
>21.28|1594582|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
AGCCGCAACTGTAGCTCCTTGGGCTTACCATAGCT
>21.29|1594649|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
TTGGACTGTTGGGTTATAGATTTGTTTGCTCATTT
>21.30|1594716|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ATAAGCAGGCACATCAGGTACAGGGGGTTTAACTGA
>21.31|1594784|34|NZ_LN831776|CRISPRCasFinder,CRT
GCCTGCTTGGTGCTGAAGACAGCGGTAAGACTTC
>21.32|1594850|36|NZ_LN831776|CRISPRCasFinder
AATCACAGAATTTGTTACAGAATTAATCTGCTGATA

CRISPR arrays and Neighbor proteins around NZ_LN831776_21

CRISPR arrays

The CRISPR arrays of NZ_LN831776_21

>merge|NZ_LN831776|21|1592755-1594917|PILER-CR,CRISPRCasFinder,CRT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAATTTTTGGTTTTTAAAGATGGAAGAGTTGTAGAGAAGTCGCTCCTTATGTGGGAGCGTGGATTGAAATAAGGCACAAGAGAGCAGCCGAGCTACAGAACGCCGTCGCTCCTTATGTGGGAGCGTGGATTGAAATAGGGCCTTATCCATTATGACTACATCATATTTTCGTCGCTCCTTATGTGGGAGCGTGGATTGAAATATGCTCTGTTTATCCTTGCTTCCGGGCCAAAAATGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCAATTGGCGGACGAACAGCAGTGGGGTTGGGTGGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCGAAACTGCCGGAAGTCGTGAAACAAATGTCCAAGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCCTAATCACTGCTACAAGCCGCGCAAGACTATGCGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCGGGCGTTGTACCAGTCCAAGAAATCACCATGTAGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATATTTGAAGCTGCACAGGAAGCCGTCCGCAGGCTCTGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATATATGGAGCAATCAAGCCTTTATCAAAATCACGAAAGTCGCTCCTTATGTGGGAGCGTGGATTGAAATACTGAAACAGTCAAAGAACTCAAAGAGGCCGTCAAGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCTGGTAGTCCATTGTTCACTCCAGCGGGATTATCGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCAGATCAATTTAACATCGTCCATACTCGCACGGTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATTATATACCGTGGATCATTATCGTGATGCTCATTTTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCATAAGATCATCCAGGATCTTGTCCTGCTTATTCGTCGCTCCTTATGTGGGAGCGTGGATTGAAATTTGCTGACAAGTGGCGAGTCTGTCATCCGCAGCACAGTCGCTCCTTATGTGGGAGCGTGGATTGAAATTGAATTCTTGCCGGATCTGATAAACCTCTTGTATGTCGCTCCTTATGTGGGAGCGTGGATTGAAATTATTTTCACCTCTGCGGTAATTGTGCCGATCCGGGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCCCATCGCCCTCGTTGATTAGTTTTTTACTTCAGTCGCTCCTTATGTTGGAGCGTGGATTGAAATCTCCGCGCTCATTACACTATTTAACTCATGTTGCGTCGCTCCTTATGTGGGAGCGTGGATTGAAATAATGAGCATGACTGCCAATAGGCTGTTCACATAGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATGCCTTGTCCCTGCATTTTGGATTTTGGCACCAATGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCAACTACTACAAAACCCCACTCGAACAATGGATTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATACTCTCTAAAGCCTCGATGTGCCATTCCTGCAATCGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCGGGTGATCGGAGGAGACGAATAATGGCAGTAGAGTCGCTCCTTATGTGGGAGCGTGGATTGAAATTGCGACCTCTGACGCAAATGCAGCAGCCGGAGAAAGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCGAATCATATTTTTAAGAATGATGGCGTGCTGCTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATAGCCGCAACTGTAGCTCCTTGGGCTTACCATAGCTGTCGCTCCTTATGCGGGAGCGTGGATTGAAATTTGGACTGTTGGGTTATAGATTTGTTTGCTCATTTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATATAAGCAGGCACATCAGGTACAGGGGGTTTAACTGAGTCGCTCCCTATGTGGGAGCGTGGATTGAAATGCCTGCTTGGTGCTGAAGACAGCGGTAAGACTTCGTCGCTTCCTATGTGGAAGCGTGGATTGAAATAATCACAGAATTTGTTACAGAATTAATCTGCTGATAGTCGCCCCCTACGCGGGAACGTGTACCAAAAT

>NZ_LN831776|21|1|1592755-1594783|PILER-CR
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TTTTGGTTTTTAAAGATGGAAGAGTTGTAGAGAA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AAGGCACAAGAGAGCAGCCGAGCTACAGAACGCC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGGGCCTTATCCATTATGACTACATCATATTTTC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATGCTCTGTTTATCCTTGCTTCCGGGCCAAAAAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CAATTGGCGGACGAACAGCAGTGGGGTTGGGTGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGAAACTGCCGGAAGTCGTGAAACAAATGTCCAAG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCTAATCACTGCTACAAGCCGCGCAAGACTATGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGGGCGTTGTACCAGTCCAAGAAATCACCATGTAG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATTTGAAGCTGCACAGGAAGCCGTCCGCAGGCTCTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATATGGAGCAATCAAGCCTTTATCAAAATCACGAAA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACTGAAACAGTCAAAGAACTCAAAGAGGCCGTCAAG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CTGGTAGTCCATTGTTCACTCCAGCGGGATTATC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CAGATCAATTTAACATCGTCCATACTCGCACGGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TATATACCGTGGATCATTATCGTGATGCTCATTTT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CATAAGATCATCCAGGATCTTGTCCTGCTTATTC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TTGCTGACAAGTGGCGAGTCTGTCATCCGCAGCACA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TGAATTCTTGCCGGATCTGATAAACCTCTTGTAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TATTTTCACCTCTGCGGTAATTGTGCCGATCCGGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCCATCGCCCTCGTTGATTAGTTTTTTACTTCA
GTCGCTCCTTATGTTGGAGCGTGGATTGAAAT	CTCCGCGCTCATTACACTATTTAACTCATGTTGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AATGAGCATGACTGCCAATAGGCTGTTCACATAG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GCCTTGTCCCTGCATTTTGGATTTTGGCACCAAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CAACTACTACAAAACCCCACTCGAACAATGGATT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACTCTCTAAAGCCTCGATGTGCCATTCCTGCAATC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGGGTGATCGGAGGAGACGAATAATGGCAGTAGA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TGCGACCTCTGACGCAAATGCAGCAGCCGGAGAAA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGAATCATATTTTTAAGAATGATGGCGTGCTGCT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGCCGCAACTGTAGCTCCTTGGGCTTACCATAGCT
GTCGCTCCTTATGCGGGAGCGTGGATTGAAAT	TTGGACTGTTGGGTTATAGATTTGTTTGCTCATTT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATAAGCAGGCACATCAGGTACAGGGGGTTTAACTGA
GTCGCTCCCTATGTGGGAGCGTGGATTGAAAT

>NZ_LN831776|21|21|1592755-1594917|CRISPRCasFinder
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TTTTGGTTTTTAAAGATGGAAGAGTTGTAGAGAA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AAGGCACAAGAGAGCAGCCGAGCTACAGAACGCC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGGGCCTTATCCATTATGACTACATCATATTTTC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATGCTCTGTTTATCCTTGCTTCCGGGCCAAAAAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CAATTGGCGGACGAACAGCAGTGGGGTTGGGTGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGAAACTGCCGGAAGTCGTGAAACAAATGTCCAAG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCTAATCACTGCTACAAGCCGCGCAAGACTATGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGGGCGTTGTACCAGTCCAAGAAATCACCATGTAG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATTTGAAGCTGCACAGGAAGCCGTCCGCAGGCTCTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATATGGAGCAATCAAGCCTTTATCAAAATCACGAAA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACTGAAACAGTCAAAGAACTCAAAGAGGCCGTCAAG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CTGGTAGTCCATTGTTCACTCCAGCGGGATTATC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CAGATCAATTTAACATCGTCCATACTCGCACGGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TATATACCGTGGATCATTATCGTGATGCTCATTTT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CATAAGATCATCCAGGATCTTGTCCTGCTTATTC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TTGCTGACAAGTGGCGAGTCTGTCATCCGCAGCACA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TGAATTCTTGCCGGATCTGATAAACCTCTTGTAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TATTTTCACCTCTGCGGTAATTGTGCCGATCCGGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCCATCGCCCTCGTTGATTAGTTTTTTACTTCA
GTCGCTCCTTATGTTGGAGCGTGGATTGAAAT	CTCCGCGCTCATTACACTATTTAACTCATGTTGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AATGAGCATGACTGCCAATAGGCTGTTCACATAG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GCCTTGTCCCTGCATTTTGGATTTTGGCACCAAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CAACTACTACAAAACCCCACTCGAACAATGGATT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACTCTCTAAAGCCTCGATGTGCCATTCCTGCAATC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGGGTGATCGGAGGAGACGAATAATGGCAGTAGA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TGCGACCTCTGACGCAAATGCAGCAGCCGGAGAAA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGAATCATATTTTTAAGAATGATGGCGTGCTGCT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGCCGCAACTGTAGCTCCTTGGGCTTACCATAGCT
GTCGCTCCTTATGCGGGAGCGTGGATTGAAAT	TTGGACTGTTGGGTTATAGATTTGTTTGCTCATTT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATAAGCAGGCACATCAGGTACAGGGGGTTTAACTGA
GTCGCTCCCTATGTGGGAGCGTGGATTGAAAT	GCCTGCTTGGTGCTGAAGACAGCGGTAAGACTTC
GTCGCTTCCTATGTGGAAGCGTGGATTGAAAT	AATCACAGAATTTGTTACAGAATTAATCTGCTGATA
GTCGCCCCCTACGCGGGAACGTGTACCAAAAT

>NZ_LN831776|21|1|1592755-1594849|CRT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TTTTGGTTTTTAAAGATGGAAGAGTTGTAGAGAA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AAGGCACAAGAGAGCAGCCGAGCTACAGAACGCC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGGGCCTTATCCATTATGACTACATCATATTTTC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATGCTCTGTTTATCCTTGCTTCCGGGCCAAAAAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CAATTGGCGGACGAACAGCAGTGGGGTTGGGTGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGAAACTGCCGGAAGTCGTGAAACAAATGTCCAAG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCTAATCACTGCTACAAGCCGCGCAAGACTATGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGGGCGTTGTACCAGTCCAAGAAATCACCATGTAG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATTTGAAGCTGCACAGGAAGCCGTCCGCAGGCTCTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATATGGAGCAATCAAGCCTTTATCAAAATCACGAAA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACTGAAACAGTCAAAGAACTCAAAGAGGCCGTCAAG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CTGGTAGTCCATTGTTCACTCCAGCGGGATTATC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CAGATCAATTTAACATCGTCCATACTCGCACGGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TATATACCGTGGATCATTATCGTGATGCTCATTTT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CATAAGATCATCCAGGATCTTGTCCTGCTTATTC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TTGCTGACAAGTGGCGAGTCTGTCATCCGCAGCACA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TGAATTCTTGCCGGATCTGATAAACCTCTTGTAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TATTTTCACCTCTGCGGTAATTGTGCCGATCCGGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCCATCGCCCTCGTTGATTAGTTTTTTACTTCA
GTCGCTCCTTATGTTGGAGCGTGGATTGAAAT	CTCCGCGCTCATTACACTATTTAACTCATGTTGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AATGAGCATGACTGCCAATAGGCTGTTCACATAG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GCCTTGTCCCTGCATTTTGGATTTTGGCACCAAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CAACTACTACAAAACCCCACTCGAACAATGGATT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACTCTCTAAAGCCTCGATGTGCCATTCCTGCAATC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGGGTGATCGGAGGAGACGAATAATGGCAGTAGA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TGCGACCTCTGACGCAAATGCAGCAGCCGGAGAAA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGAATCATATTTTTAAGAATGATGGCGTGCTGCT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGCCGCAACTGTAGCTCCTTGGGCTTACCATAGCT
GTCGCTCCTTATGCGGGAGCGTGGATTGAAAT	TTGGACTGTTGGGTTATAGATTTGTTTGCTCATTT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATAAGCAGGCACATCAGGTACAGGGGGTTTAACTGA
GTCGCTCCCTATGTGGGAGCGTGGATTGAAAT	GCCTGCTTGGTGCTGAAGACAGCGGTAAGACTTC
GTCGCTTCCTATGTGGAAGCGTGGATTGAAAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_039787082.1|1579384_1581607_+|RNA-binding-transcriptional-accessory-protein	unknown	unknown	gnl|CDD|225094
NZ_LN831776.1|WP_052741421.1|1601927_1602917_+|hypothetical-protein	PD-DExK	mkCas0090_PD-DExK_CAS-I:CAS-III	unknown
NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	gnl|CDD|273847
NZ_LN831776.1|WP_020427474.1|1578061_1579288_+|tetracycline-resistance-MFS-efflux-pump	unknown	unknown	gnl|CDD|340883
NZ_LN831776.1|WP_020427479.1|1586271_1587297_-|hypothetical-protein	unknown	unknown	gnl|CDD|226355
NZ_LN831776.1|WP_046501621.1|1590447_1592427_+|TetM/TetW/TetO/TetS-family-tetracycline-resistance-ribosomal-protection-protein	unknown	unknown	gnl|CDD|223556
NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	gnl|CDD|224124
NZ_LN831776.1|WP_020431432.1|1596667_1598527_+|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	cas10	cls000742_cas10_CAS-III	gnl|CDD|274208
NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	gnl|CDD|187887
NZ_LN831776.1|WP_020427617.1|1576832_1577441_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_LN831776.1|WP_020427476.1|1582654_1583527_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831776.1|WP_046501615.1|1587521_1588331_+|hypothetical-protein	unknown	unknown	gnl|CDD|237030
NZ_LN831776.1|WP_081487144.1|1583674_1585027_+|GntP-family-permease	unknown	unknown	gnl|CDD|225330
NZ_LN831776.1|WP_020427482.1|1588762_1589755_-|S-layer-homology-domain-containing-protein	unknown	unknown	gnl|CDD|306825
NZ_LN831776.1|WP_020431435.1|1600719_1601094_+|type-III-B-CRISPR-module-associated-protein-Cmr5	cmr5gr11	COG3337_cmr5gr11_CAS-III-B	gnl|CDD|378242
NZ_LN831776.1|WP_020431433.1|1598495_1599794_+|type-III-B-CRISPR-module-associated-protein-Cmr3	cmr3gr5	pfam09700_cmr3gr5_CAS-III-B	gnl|CDD|370625
NZ_LN831776.1|WP_020431434.1|1599790_1600720_+|type-III-B-CRISPR-module-RAMP-protein-Cmr4	cmr4gr7	cd09682_cmr4gr7_CAS-III-B	gnl|CDD|274210
NZ_LN831776.1|WP_039787092.1|1585062_1586211_+|glycerate-kinase	unknown	unknown	gnl|CDD|376844
NZ_LN831776.1|WP_167345589.1|1595246_1596710_+|type-III-B-CRISPR-module-RAMP-protein-Cmr1	cmr1gr7	COG1367_cmr1gr7_CAS-III-B	gnl|CDD|224286
NZ_LN831776.1|WP_020431436.1|1601115_1601931_+|type-III-B-CRISPR-module-RAMP-protein-Cmr6	cmr6gr7	COG1604_cmr6gr7_CAS-III-B	gnl|CDD|224520

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831776.1|WP_020431435.1|1600719_1601094_+|type-III-B-CRISPR-module-associated-protein-Cmr5	cmr5gr11	COG3337_cmr5gr11_CAS-III-B	4.9e-21	69.9	0.0
NZ_LN831776.1|WP_020431436.1|1601115_1601931_+|type-III-B-CRISPR-module-RAMP-protein-Cmr6	cmr6gr7	COG1604_cmr6gr7_CAS-III-B	1.3e-50	167.1	0.0
NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	1e-60	199.7	0.0
NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	7.7e-161	531.0	1.6
NZ_LN831776.1|WP_052741421.1|1601927_1602917_+|hypothetical-protein	PD-DExK	mkCas0090_PD-DExK_CAS-I:CAS-III	8.9e-27	87.9	0.3
NZ_LN831776.1|WP_020431433.1|1598495_1599794_+|type-III-B-CRISPR-module-associated-protein-Cmr3	cmr3gr5	pfam09700_cmr3gr5_CAS-III-B	1.3e-72	240.0	0.0
NZ_LN831776.1|WP_020431434.1|1599790_1600720_+|type-III-B-CRISPR-module-RAMP-protein-Cmr4	cmr4gr7	cd09682_cmr4gr7_CAS-III-B	1.9e-74	245.5	0.0
NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	3.3e-85	281.5	7.6
NZ_LN831776.1|WP_167345589.1|1595246_1596710_+|type-III-B-CRISPR-module-RAMP-protein-Cmr1	cmr1gr7	COG1367_cmr1gr7_CAS-III-B	1.7e-65	216.2	0.0
NZ_LN831776.1|WP_020431432.1|1596667_1598527_+|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	cas10	cls000742_cas10_CAS-III	1.2e-78	259.7	4.1

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_039787082.1|1579384_1581607_+|RNA-binding-transcriptional-accessory-protein	gnl|CDD|225094	COG2183, Tex, Transcriptional accessory protein [Transcription].	0
NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3	gnl|CDD|224124	COG1203, COG1203, CRISPR-associated helicase Cas3 [Defense mechanisms].	7.24875e-69
NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5	gnl|CDD|273847	TIGR01876, cas_Cas5d, CRISPR-associated protein Cas5, subtype I-C/DVULG. CRISPR is a term for Clustered, Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This small Cas family is represented by CT1134 of Chlorobium tepidum. This family belongs to a set of several Cas protein families, one each for a number of different CRISPR/Cas subtypes, that share a region of N-terminal sequence similarity modeled by TIGR02593. This family represents the Dvulg subtype of CRISPR/Cas locus.	3.09357e-90
NZ_LN831776.1|WP_020427474.1|1578061_1579288_+|tetracycline-resistance-MFS-efflux-pump	gnl|CDD|340883	cd17325, MFS_MdtG_SLC18_like, bacterial MdtG-like and eukaryotic solute carrier 18 (SLC18) family of the Major Facilitator Superfamily of transporters. This family is composed of eukaryotic solute carrier 18 (SLC18) family transporters and related bacterial multidrug resistance (MDR) transporters including several proteins from Escherichia coli such as multidrug resistance protein MdtG, from Bacillus subtilis such as multidrug resistance proteins 1 (Bmr1) and 2 (Bmr2), and from Staphylococcus aureus such as quinolone resistance protein NorA. The family also includes Escherichia coli arabinose efflux transporters YfcJ and YhhS. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. The SLC18 transporter family includes vesicular monoamine transporters (VAT1 and VAT2), vesicular acetylcholine transporter (VAChT), and SLC18B1, which is proposed to be a vesicular polyamine transporter (VPAT). The MdtG/SLC18 family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.00212e-73
NZ_LN831776.1|WP_020427479.1|1586271_1587297_-|hypothetical-protein	gnl|CDD|226355	COG3835, CdaR, Sugar diacid utilization regulator [Transcription / Signal transduction mechanisms].	2.96607e-75
NZ_LN831776.1|WP_046501621.1|1590447_1592427_+|TetM/TetW/TetO/TetS-family-tetracycline-resistance-ribosomal-protection-protein	gnl|CDD|223556	COG0480, FusA, Translation elongation factors (GTPases) [Translation, ribosomal structure and biogenesis].	1.92368e-170
NZ_LN831776.1|WP_020431432.1|1596667_1598527_+|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	gnl|CDD|274208	TIGR02577, thermophile-specific_DNA_repair_system, CRISPR-associated protein Cas10/Cmr2, subtype III-B. This model represent a Crm2 family of the CRISPR-associated RAMP module, a set of six genes recurring found together in prokaryotic genomes. This gene cluster is found only in species with CRISPR repeats, usually near the repeats themselves. Because most of the six (but not this family) contain RAMP domains, and because its appearance in a genome appears to depend on other CRISPR-associated Cas genes, the set is designated the CRISPR RAMP module. This protein, typified by TM1794 from Thermotoga maritima, is designated Crm2, for CRISPR RAMP Module protein 2.	1.72839e-72
NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	gnl|CDD|187887	cd09757, Cas8c_I-C, CRISPR/Cas system-associated protein Cas8c. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Zn-finger domain containing protein, distant homologs of Cas8 proteins; signature gene for I-C subtype; also known as Csd1 family.	2.89947e-169
NZ_LN831776.1|WP_020427617.1|1576832_1577441_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	9.02096e-18
NZ_LN831776.1|WP_020427476.1|1582654_1583527_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	1.57991e-13
NZ_LN831776.1|WP_046501615.1|1587521_1588331_+|hypothetical-protein	gnl|CDD|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	1.69539e-09
NZ_LN831776.1|WP_081487144.1|1583674_1585027_+|GntP-family-permease	gnl|CDD|225330	COG2610, GntT, H+/gluconate symporter and related permeases [Carbohydrate transport and metabolism / Amino acid transport and metabolism].	3.05901e-55
NZ_LN831776.1|WP_020427482.1|1588762_1589755_-|S-layer-homology-domain-containing-protein	gnl|CDD|306825	pfam00395, SLH, S-layer homology domain.	9.58091e-06
NZ_LN831776.1|WP_020431435.1|1600719_1601094_+|type-III-B-CRISPR-module-associated-protein-Cmr5	gnl|CDD|378242	pfam09701, Cas_Cmr5, CRISPR-associated protein (Cas_Cmr5). CRISPR is a term for Clustered, Regularly Interspaced Short Palindromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This family, represented by TM1791.1 of Thermotoga maritima, is found in both archaeal and bacterial species.	2.24088e-19
NZ_LN831776.1|WP_020431433.1|1598495_1599794_+|type-III-B-CRISPR-module-associated-protein-Cmr3	gnl|CDD|370625	pfam09700, Cas_Cmr3, CRISPR-associated protein (Cas_Cmr3). CRISPR is a term for Clustered Regularly Interspaced Short Palindromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR associated) proteins. This highly divergent family, found in at least ten different archaeal and bacterial species, is represented by TM1793 from Thermotoga maritima.	9.36311e-74
NZ_LN831776.1|WP_020431434.1|1599790_1600720_+|type-III-B-CRISPR-module-RAMP-protein-Cmr4	gnl|CDD|274210	TIGR02580, putative_CRISPR-associated_protein, CRISPR type III-B/RAMP module RAMP protein Cmr4. This model represents a CRISPR-associated protein from the family that includes TM1792 of Thermotoga maritima. This family is part of the broad RAMP superfamily (pfam03787) collection of CRISPR-associated proteins. It is the fourth of a recurring set of six proteins, four of are in the RAMP superfamily, that we designate the CRISPR RAMP module.	6.03973e-78
NZ_LN831776.1|WP_039787092.1|1585062_1586211_+|glycerate-kinase	gnl|CDD|376844	pfam02595, Gly_kinase, Glycerate kinase family. This is family of Glycerate kinases.	0
NZ_LN831776.1|WP_167345589.1|1595246_1596710_+|type-III-B-CRISPR-module-RAMP-protein-Cmr1	gnl|CDD|224286	COG1367, COG1367, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	1.88045e-53
NZ_LN831776.1|WP_020431436.1|1601115_1601931_+|type-III-B-CRISPR-module-RAMP-protein-Cmr6	gnl|CDD|224520	COG1604, COG1604, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	6.42086e-57

Protein sequences

>NZ_LN831776.1|WP_046501621.1|1590447_1592427_+|TetM/TetW/TetO/TetS-family-tetracycline-resistance-ribosomal-protection-protein
MVQQQGMERINVGIFAHVDAGKTTTTEHILYESGRIKAVDSVDSGTALTDSMEVERQRGISVRAALASFEWRGVQVNLVDTPGHVDFLSEVERSLRVMDCAVLILSAVEGVQAQSEMIWNALRKLGIPTLVFLNKMDRTGADPEAVLVQARTYLSGDILPVQQALGQEQEYAGAVDLWAEAADPAARIELLEALAERDEALLETYMSDTPLDLTAWKEQLKAGAAAGRWFPLVYGVAAKGLGITQLLDAMTDYFPRAGGNPQLPVSGIVYSIQRDKTMGRMAYVRLYQGMVRNRDTVMNYTQDVQGKVTQIRKVEGGRTEDVGTLEAGDIAVVYGLSGVKIGDVLGVPDAVPQEAKLAVPLLTVRVHWDAAVDEHKVIGAFQELADEDPLLDTQWLQDERELHIKVMGPIQLEILDSVLESRYGLKVTFGQPSVIYRETPSRAGEGYVAYLMPKPCWAILRFRIEPGPPGSGLRYESLVRSSDLLPQYQNETARRVPEALMQGLYGWEVTDLKVTLTEGQHHVWHTHPLDFAVATPMAIMDGLNRVGTKLLEPILQVRIVVPEENGGRVMNDLVQMRGTFEPPVLQGERMIIEGRLPLATSLDYPVSLSSYTKGRSTFTSFFAGYEECPPDVRAERTRRGVNPLDQARYILSVRKALQG
>NZ_LN831776.1|WP_020427482.1|1588762_1589755_-|S-layer-homology-domain-containing-protein
MNKYSFQMSAKKITIACGILAASVSFGASAFAFSDIKGDPAESKINALHNKGVVNGVTTDRFAPKSKVTFAQGIQFIVNGLQLSPKASGGGSTVTSSVYFDKVKDKAWYASAFLIAKQNGLTLDKSVDPNAAMTRIQFAHLLTQALQSKGNFPVTLMYADISDGSKLSNAEMNSLQILVNTHLVTLEKNNTFRPNDAVTRAEAAVWIYDAAEFAQTVITPEVTPPDEGTAAPAQLYEGSITLEKAGQGVNKVTLTVNDLPNPGYGLAINRIEFGKDKTAVIYFSVTKPDPGKMYPMVITKGTAVTYLPEGYTATAKSLTAAPSSSGSSVR
>NZ_LN831776.1|WP_046501615.1|1587521_1588331_+|hypothetical-protein
MITVKKILGHSALAALLLVLAACNSASEAEPQQTQGSPSPSASASAAPSASASAAPSASASAAPSTSASAVPSAPASAAPASSEPAESQVPQASGAPEEGTPPTAMEAATTVLRALSRGNMETLASWAHPDKGVRFSPYAHVDTATDLVFTRDQLEGLMKDSKPYVWGKFAGSGEAIKLTFAEYFKRFVYDADFMNKAETALNKGLGQGTTLNNINEVYPKDSYDFVEYHIAGVDPANEGMDWRSLRLVFEKMGEDRALVGIVHDQWTP
>NZ_LN831776.1|WP_020427479.1|1586271_1587297_-|hypothetical-protein
MFQLSENQAQEIVDKMMTDIPYNINIMNADGIIIGSGRRERIGTVHQGAVQALSTGRMVEVWEDSRFEKKGTNEPIVIGHTRVGVIGISGNPDEVRPFCNIVRTTVSLLIEQRNSLETLAHEANRKKAFLELLLNHQGAYSQKLRKEAAPYQIDLLLKTVVLYIKHFNAEADPDKLLLRYPSFAIDEETQLLILQESGDPGPLIRELLRGQPQVLIAAGKQEASIAESYRQARSAMNILLALKPAAQVIAFENVEFLVKLSHASLAPLNTAAKLEDAVDMIETLRSFINHNCSVSHTADDLNIHRNTLQYRLKRIQALTGKDPRNLLQLFELTHGLLALYK
>NZ_LN831776.1|WP_039787092.1|1585062_1586211_+|glycerate-kinase
MKGKEKTFVLAPDSFKESMTAKEVCIAMEKGLRKVYPAAHYIHVPMADGGEGTVQSLVDASGGEIHYKEVNGPLGQKVTAKYGILGGGQTAAIEMASASGIHLVPKETRNPLITTTYGTGELIRECLDRGIRKIIIGIGGSATNDGGAGMAEALGARFLDESGAELPRGGGSLDRLASIDISALDERLQHVQMIVACDVTNPLCGEQGASRVFGPQKGATPEMVQKLDANLAHYAAVVKQQLHKDVRDLPGAGAAGGLGAGLLIFTQAVLQKGIEIVIEYTGLKEKLAGADVVFTGEGGIDFQTKFGKTPYGVARAAKAGGQKVIAVAGYIGEGIDALYEEGFTAIFGIVPGASGLEKLLAEGPQNVERTCENIARILKLSE
>NZ_LN831776.1|WP_081487144.1|1583674_1585027_+|GntP-family-permease
MRPAFILKACSTRVIGGCTMEGLTIGWYGALAGLALAIILILRKLNPVYSLFLGAIAGALIGGANLEQTVSVLVSGTQSVMGTVLRVLAAGVLAGVMMESGAAETIAQAIVKKFGGSKAILALALATMIITAVGVFIPVAVLIVAPIALSVGNKMGISKMALLLALSGGGKAGNIISPNPNTIAAARGFDLDLSHVMLAGFIPAVCGLIVTVIVASLLKNKGVRVLDGEAVYNEIDTSKYPPLGKAIVAPLVAVILLMINPIGSLTGIDALSRIKVDALYILPVAGIIGLLAMGQGNKILAFTSSGLNKMTATVLILIGAGGIAGLIAASDLSVQIVSLIQAAGISGTFLAPISGILMAAATGSTSTGVILATGSFGQAILNMGTAPLAAAVMVHTGATVIDSLPQGNYFHVTADSMKMSIKQRMGLIPYEAVVGGTMAVAATVIYGFLL
>NZ_LN831776.1|WP_020427476.1|1582654_1583527_+|GNAT-family-N-acetyltransferase
MAALGEFYQVVTASGPVIFWWVGEEENYENVLCAFEGNQMVAKGQVGVFNVIPNESTAENKHRIFINLKVVPGREEDVELLNGVYERLLARAVAVKETLPEGHGTLLCVGNYSTETGYHRYFQEQQGYQYLHSLYSLQRDLTQPVVEMPLTEGLDWIHWGMETREEQNQYMKLESEVWPDAPIGAERLAEYRAHPLWTAIIAREAGTRVASVMVWQEDAGGVIEDVFVREAWRRRGIARFLLAEALKYLQGHGLETASLITGTDNHSAQALYQSVGFHIESEEIRYYIEL
>NZ_LN831776.1|WP_039787082.1|1579384_1581607_+|RNA-binding-transcriptional-accessory-protein
MDTNQAGPAAEEALARQEQETITQAIAKELGISVKQVRTTVGLLDEGNTIPFIARYRKEMTGELDENVLRDIEERLSYLRNLGDRKKDVLRSIEEQGKLTKELQEQILKAVKLQEVEDLYRPFRQKRKTRASAAKEKGLEPLADWVMEQRRQGQPLEEAAKYIDADKGVESAELALQGAMDIIAENIADDPAVRSWVRQYTASQGILVSEAKDAEQESVYENYYNYREPVHKMPPHRILAINRGERENVLKVGIEVTADKIHAFILRKLVKGPSPVKELLEAVTEDAYKRLIAPSVEREVRGEMTEKGETQAIAIFSGNLRSLLLQPPVKGRNVLGVDPAYRTGCKLAVVDDTGKLLEVAVTYPTPPNNKKKEAAAKFKELIAKYGIQLIVIGNGTGSRETEQFTAEVIAEIGDPGLAYLIVNEAGASVYSASKLAQEEFPDLDVAERSAASIARRVQDPLAELVKIDPKAIGVGQYQHDVSQKHLEESLKGVVESAVNHVGVDVNTASASLLSYVAGVNSTIAKNIVKFREENGKFTTRKQLQKVPRLGAKSYEQCIGFLRIPGGDNTLDRTPIHPESYPVVDRLFRELGLDVASLGSKEVAEQLQAQDAAELAVKLDVGVPTLRDILESLQRPGRDPREELPPPIFRTDVLKIEDLVPGMEMQGTVRNVIDFGAFVDIGIKNDGLVHISQLSGSYVKHPMDVVSVGDNVTVWVMGVDLKKGRVSLTMRPPRDNNGGAK
>NZ_LN831776.1|WP_020427474.1|1578061_1579288_+|tetracycline-resistance-MFS-efflux-pump
MTLLLRNRGAMLLLMLNIFLAFTGIGLVVPIMPTYMNELGIGGSIVGLLVAAFSLTQLILSPLAGGLSDRMGRKKIIVGGLVVFALSELLFGLAESSWLLFASRMLGGAGAAMIMPAVMAYVADTTSMEERAKGMGLINAAITTGFIIGPGLGGYLAELGIRVPFFAAAGAAAFVAVMTLFVLPESRSSAELGAAKSTQENKDSKDSLITQLVRSYREPYFFGLVIVFVLSFGLANYETVFGLFVDHKFGFTPKDIAFVITFGSISGAVIQVTAFSWILNRFGENKVISASLLVSGLSILLTLFVHGYWAIVTVTFIVFLAMDILRPAVGTQLSKMASESQQGFVMGMNSAYTSLGNIAGPIVAGVLFDLDINLPYTVAALVLMLCFIMSLGSRKRMNRPDLQAKQAD
>NZ_LN831776.1|WP_020427617.1|1576832_1577441_+|TetR/AcrR-family-transcriptional-regulator
MIRIKGRSDGEETKKRIVQKAAQLFVQKGYGAVTMNEVCSAAKVSKGSLYHHFPSKDELFLYVVEDDTEQWLSQWAEKSRSISGLEERFYALGEHYANDFQNPLIRALEEYARARPHSDEVHQRLAQLYESASEACRNLLQEGMDSGYLVKGDLDNYVIVVSGLLEGVARVSEIMAAAKAPEDIMQYYREAIGLLLQGIRAR
>NZ_LN831776.1|WP_167345589.1|1595246_1596710_+|type-III-B-CRISPR-module-RAMP-protein-Cmr1
MDPKKEIKPPTLDLVIKDIQESRKKVPEDRFNITIVTPMFGGGSKPGFTDSAFPIRSASIRGHLRFWWRATRGAAFESVTELRQREVEIFGDSHSPSRVKISVHIFNKTEPEKGKEHSASINNETPKRTVRLPRYAVFPFDKNNPGSNMQQFELTIRYTPRLPKQADTLENGSKPFLNVEQLRKEITPALWAWINFGGLGSRTRRGCGSLYCKDFAPERTSTHPKYEDWFHGKVADYELELDTQLEKKEWPTLSRSVIIQEYERDMISAWNDVIKLYHNFRSQPNNTYIYSKPPKYERSLWPEADSLRRVTGMSEEDHKKPSPFKKQEFFSFPRAQLGLPIIFQFKQDEYLKKRYSNFREPYNMQLAPKDKSRLASPLITKALARSDKRGVGIIVKLNQPRLSELELKVIENKEDKRKRSPRDFAHIESIEELVAHKPIREKDIYKELSYPGSPMKQGQKSAIQAFLESEEVKEWKRTSYRPNPKQK
>NZ_LN831776.1|WP_020431432.1|1596667_1598527_+|type-III-B-CRISPR-associated-protein-Cas10/Cmr2
MEENFLQAEPQTEVVMLISIGPVQEFIAQARKTRDLWFGSHLLSEISKEAARRLAEAHNARMIFPYIHKEKIAYGLDDLKVANKVLAIVPTNDPKAVALDVRRAVVTKWLGYANKAKEELGSGIIGPMWERQVKDFIEFYAVWSELESEEKYAEVLQQTEQLMAARKTLRDFRPNEPADLFGDDKSGLDSGRESVLKPSQYMSYAGFGIKHKETLDAISLVKRLSRFTVDKKEFKSVCDVAFQQFRDELGASRNQWMKTAVDEYYRDLKHKYGTALKLTGSDLQSYKSEMFYTSRVEEAVVELAAEMKKPINRVKQLEITQNILTSLEELYGKILKEPTPYYALVVGDGDRMGDALRKMKTPAEHQSFTEHLSGFASEVERIVFKDDIKGQMIYSGGDDLMALLPVHRCLAAAQEIRQAFTNTMTLALPDEDQRPTLSVGIAIVHMFEPLEDSLLIARAAEALAKVRRDELAIHFQKRSGSEEMRVSLPFSENPVNTIVKLQSLYRNRYISTSFAYGLRQLHAEYLDLKAHGSLQNEGMGELLYFEIRRLLLLKKPEFKSKDEIIKEVLSVFKGLEQTDSDRVKDPLVLLNRLAEQCVIAVTLEKVGGAYGTNDTNSTS
>NZ_LN831776.1|WP_020431433.1|1598495_1599794_+|type-III-B-CRISPR-module-associated-protein-Cmr3
MERTIQIQPLDPLMIRDGRPFGNTPGARAHTLGTVTPGVVAGTLRTLMQKNNTAGTFGTTTKDAEREGKPSTVAKVDIRGPLYMLNDRLFLPMPYDLDLYEPGLQEDPASIHVNVRRPIEPAKNTPTHLHGFLGTGKTSLHEDKLWPVSMDTEIRKPLKSAPAYISAEWMIKWLCDNLQPEQWSAAIAEWRSKPEDKVHFIAPFVKEVRTHTAIQAETSTVQDKALFSTESLVIPPDVSLIASASIGSDVKWEGTISGIHSFGGKRRLAHFREIDDQEIQDNIWKCPEAIAQAVAENPRYLRMVLATSAYFSKGWLPGWLDGDLRSTDRFDKQLQIELCWACLPRWEGISGWSYRHNQPKAVRRMVAAGSVYFFKVISGDPVEFVRRNWLTSMSDEDRRKAFFDKQDGYGLATWGVWTPYGHHKGMDKGDIR
>NZ_LN831776.1|WP_020431434.1|1599790_1600720_+|type-III-B-CRISPR-module-RAMP-protein-Cmr4
MTNNRLYYVHCMSSVHIGTGQGVGIIDMPMIREKVTEWPYLPGSSMKGVHRVFFKSGIHKQPEKWLNSAFGKASNKGTNFNSDDGFELDDGNAGALVMSDAKILAFPVASRYGTFAYVTCPLVLKRFRRDTVAAGVDMPEFDWAALESVVNSGVVMLHTDSKLDKNNEVFVDEFTSGAVKDEAFAKWTDWLAGQIFVKDELSETMLKERMLLVSDEAFQYFVSMCSEVVPRIRIGLETGSVEPGALWNEEYLPVESILYGVIWSDGISVKTLENRGLLDIFPEEAFLQIGGNATVGKGRIRCRYVKGGA
>NZ_LN831776.1|WP_020431435.1|1600719_1601094_+|type-III-B-CRISPR-module-associated-protein-Cmr5
MKSAAHTYAEKAMQSIRSVEADPDCNNKDYGRLCLLFPSMVQVNGLRLTVAFFQSKGKSQKTLHQRYLQDLAAAVGSAAWETGLSTNDMMDYRDLTRHVLQAAVWFKRYAEAILKVEAADGLDS
>NZ_LN831776.1|WP_020431436.1|1601115_1601931_+|type-III-B-CRISPR-module-RAMP-protein-Cmr6
MNAYLAITKQEASNKGSKLYRVVNGDLQNTKGEFYRQLIKEYQADWKQSCIWYEQRYEHYSTKLHDTLGDSRCIEFEMASISPLLIGHGGVSALETSLMLHRIYGVPYIPGSAIKGVTANYCHCMLGAENPAFLSDGEYYEALFGSQDQAGYINYEDAWVTPATAESALIDDVMTPHHQNYNSIQLQRTDQQKASAPRDDDDPVPLPFLAVNASFRFLLTCPSDRVEKEDARQWLNIAQEIVSHALQYEGIGGKTNAGYGRMLQADRRERE
>NZ_LN831776.1|WP_052741421.1|1601927_1602917_+|hypothetical-protein
MKDKQPSSEQELEEMRKAAPKIIQQIAQNYIHLEESITSQLRMAAGSHHVTSGTFREDIWKSLFEQIIPRKFSIEQSVFIIDSHGLVSKEVDLAIFDEQYTPYIFRLGRIKYIPIEAVAVVVQCKSNNIHGRNKRENLRTWSKSITNLKTSLKSVARIHTGIAKGEYDYILDKDGQLRIEPEKLEKSDRDKLAQTSTRPIQILCHTKDTSSSKYDDLFDIVIHPEGERLRVEMKPDLKDLPSWYDSLNHKQDPRYEHIVKPFDTKEPSEDFQKALQVDNYKVYKDKARTKEIGLLSLTFQLNQLLMLINNPILFPHMAYVDMFNTNISK
>NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3
MEYIAHIRESDMKVQTVTEHLLEVRTLAEKYGKKLGIKYMAGLAGMLHDLGKYTEEFRNYIVQAVYHPEAPPSRGSVDHSTAGGKLLFERFHRVPADLSNKEAHINKMILAEVVGNAILSHHSYLQDFLNPDSESNFLNRVQDKCLPEFERAKDSFFELVMNETEFHLYVDKAVEELSDYLKVDSSSTTELKLMFLTKYVFSALIDADRTNTRCFEENQPDPSYNPQQLFSAYYTKLMTKIDSFHNHKHAHSAINQLRQGMSEQCEQFAAEPSGIYTLSIPTGGGKTLASLRYALKHALLKEKKHIIYVVPYTTIIEQNANEIRSILKDDEHILEHHSNVVEEETQDDEHEDGSLSLRQKLKLAKDNWDAPIIFTTMVQFLNVFYADGSRNIRRLHNLSESVIVFDEVQKVPVRCVSLFNQALNFLKSYAHSSIVLCTATQPELDYVRLKLEIEPEAEMIHNLDHVIEAFRRVEIVDRATNEHFDNDTLTEFVITQMREVSSVLVILNTKSVVQALYRSLNERNLSVPIYHLSTSMCAAHRNQILDKVKALLEDKEPVICISTQLIEAGVDVSFQCVIRSLAGLDSIAQAAGRCNRHGEDLIRQVYVIDHIEENLKHLKEIKIGKEISRKILIDLSRDASLHGGHILSIQAMEKYFKEFYTELATSLNYSIPKLGQEMTTLLSGPRKNNAYYQAYLSKHRAALPLFLLNSYKTAAENFQVIDNLTTTVVVPFGDGPEEGKDIIAELNGQQSIPDLTRLLRKAQQYTINIYSYEKDLLSKNGSLVPYLDGKILALKEGAYHPEYGLNLENDSPLDMYMF
>NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5
MRNSIEFKVYGKYALFTDPLTKLGGEKLTYSVPTYQALKGIVESIYWKPTIHIIVEEVRIMNAIRMESKGIRPMDYGGGNTLANYTYLKDVCYEVRAHFEFNMNRPDLEHDRNEHKHHNLLKRSLQAGGRRDIFLGARECQAYVEPCVFGVERGFYNDYGDIHLGSMVHGINYPDETGRDEMEVRLWSPVMRDGIIRFIRPEECTQVRRIAEMKPKSFNETNLQTAEELLAQIEAEEKA
>NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1
MSWLLNLYETYQSNQDCVGVIETRYNDREYTLLPVSHTTQNAHIEVNVTEDGEFHSASVLDKSESSTLIPCTEDSASRAGSKVAPYPLHDKLSYVAGDFLAYGGKIKKEEPFAAYIKQLGGWADSPYACPKVKSIHSYLSKRRLIQDLVSHSILFLDADHQLIEKWDKKYEALHGEKPLIFSAVAGEQESAFIRFNVYSPDKELTKVWKDPEMYDSFMQYYSHLLGQEDYCYVTGRMLPSTDRHANKIRNAADKAKLISSNDTSGFTFRGRFTQSSDAASISYEVSQKAHNALKWLINRQGKIVDQRVFLVWGNDDLNIPDPTEDFFSFDLEPAVARERKSYTHKEYAGEIAKAMDGYRNKLASEYKSDVNILVLDSATTGRLAVLYYRNMDKQLYLDKLVHWHSTCSWLHRYRKNTQDEWVEFYGASATKDIAFAAYGPKANEKIVKGVMERLLPCIVDGHNIPQDIVRSAFYRASNPVSMEKWEWEKTLSITCALINAKEEMNVALDTEIDDRSYLFGRLLAIADVLERRALDSDEKRSTNAIRYMNAFSQHPERTWNTIQQSIQPHQARLGTKLRYYSSLIDEVASKIPLDQFNNKPLSGKYLLGFYSQRHELYQKKDKNNDSIQASENGER

Crispr_ID: NZ_LN831776_22

• CRISPR_ID: NZ_LN831776_22
• CRISPR_location: 1603409-1605507
• CRISPR_type: TypeIII
• Repeat_type: I-C
• Spacer_info: 31 spacers
• Cas_protein_info: PD-DExK,cmr6gr7,cmr5gr11,cmr4gr7,cmr3gr5,cas10,cmr1gr7,cas3,cas5,cas8c,cas7,cas4,cas1,cas2

Consensus repeat of NZ_LN831776_22

Consensus_repeat	Method
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	PILER-CR
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CRISPRCasFinder
GTCGCTCTCTATATGGGAGCGTGGATTGAAATN	CRT

spacers of NZ_LN831776_22

>22.1|1603441|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ATTTCCAAGGCTACCATACATCCCAAAATCAGTAA
>22.2|1603508|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ACCAATCTTGATAAAGATCAGAAATACAAACTTG
>22.3|1603574|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
TGTGATCCGGGAGCAGGGCGCTTTGTGTTCAGC
>22.4|1603639|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CCTATCGGGCAAAATTGTAGGCCCGGATGCTGCCA
>22.5|1603706|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CAATGGACGAATTAGAGCTTCTGCTAGAAAAAT
>22.6|1603771|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ATTTTACTACCATCCTTTCCCATGAAGTATGTTA
>22.7|1603837|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
GCCCTCTATTGGGCCGGCTTAGATGAAGAAGAGGAA
>22.8|1603905|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CTGTATACTCTCGAACAAAATTATTGATGCTAT
>22.9|1603970|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CACAACGATTCAATCTTTTGGTTGATCTCCCCGGC
>22.10|1604037|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
GGTATCAACGCCAAGATCGTTCATCAACGATTTAAC
>22.11|1604105|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
AAAGGTACCAACGGCCAGAATGCTGCCTTTTCGT
>22.12|1604171|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
TTGAAATCTTGATACTCTACTCCGGCGGCCTTAT
>22.13|1604237|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ACCGACCTTTGCGATGTCGGATGCTGATTGAGGC
>22.14|1604303|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
AATACGGTTATGAGATTGCTATCTATAGAACCTC
>22.15|1604369|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
GGCGGGATGGCCCAGGATATTAACAACTGGTCGAA
>22.16|1604436|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
GATTACGTCCAGCCGATTCGCATCATCTACTTTGG
>22.17|1604503|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
TATCACACCGGGAACGGTTTGAATTTAGAGTATAT
>22.18|1604570|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CAGGAACGAAGGAGTATGCAGATTATCAGAAGCGC
>22.19|1604637|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CCGCTGATTGGGTAAGGTACTTTTTATCAAATGATG
>22.20|1604705|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CTCTTTGGAGGGCTTATTTGTGGCTCCTATGCTGTT
>22.21|1604773|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CACCAGGGACGCCAGGAAGGCCGTCCGCACCTGGG
>22.22|1604840|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ACTGGGAGTGTTGCACCATTTGGTTATAGAAAAA
>22.23|1604906|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CACTACCTGCTGCTCATTGAGCATCCGGGGGATTG
>22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
AGGTTGTCGGTGACGTTACGGTCAAAGATGACTT
>22.25|1605039|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
GACCTTCCAGGCGCCGCCGTCTGCCTCGATCAGGG
>22.26|1605106|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ATAATGCGGCTACAGTCACCCGAGGCGACAAAGG
>22.27|1605172|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
AGTTGATGATCGAGGAACAGCATTTACCAGTATCAA
>22.28|1605240|35|NZ_LN831776|CRISPRCasFinder,CRT
TTGGCAGCATTAACATATCCACGATTAGCACTTGT
>22.29|1605307|33|NZ_LN831776|CRISPRCasFinder,CRT
CCTCCTGGAGTTTCGCTTGATATTCCAAATCAC
>22.30|1605372|37|NZ_LN831776|CRISPRCasFinder,CRT
CAAGGCAAGCGCTATCGCCTTGGTAAACGGGTTGATA
>22.31|1605441|35|NZ_LN831776|CRT
CGTTTGAGCTCGGCGTTGCTCCATTCCTTTACTTG

CRISPR arrays and Neighbor proteins around NZ_LN831776_22

CRISPR arrays

The CRISPR arrays of NZ_LN831776_22

>merge|NZ_LN831776|22|1603409-1605507|PILER-CR,CRISPRCasFinder,CRT
GTCGCTCTCTATATGGGAGCGTGGATTGAAATATTTCCAAGGCTACCATACATCCCAAAATCAGTAAGTCGCTCTCTATATGGGAGCGTGGATTGAAATACCAATCTTGATAAAGATCAGAAATACAAACTTGGTCGCTCTCTATATGGGAGCGTGGATTGAAATTGTGATCCGGGAGCAGGGCGCTTTGTGTTCAGCGTCGCTCTCTATATGGGAGCGTGGATTGAAATCCTATCGGGCAAAATTGTAGGCCCGGATGCTGCCAGTCGCTCTCTATATGGGAGCGTGGATTGAAATCAATGGACGAATTAGAGCTTCTGCTAGAAAAATGTCGCTCTCTATATGGGAGCGTGGATTGAAATATTTTACTACCATCCTTTCCCATGAAGTATGTTAGTCGCTCTCTATATGGGAGCGTGGATTGAAATGCCCTCTATTGGGCCGGCTTAGATGAAGAAGAGGAAGTCGCTCTCTATATGGGAGCGTGGATTGAAATCTGTATACTCTCGAACAAAATTATTGATGCTATGTCGCTCTCTATATGGGAGCGTGGATTGAAATCACAACGATTCAATCTTTTGGTTGATCTCCCCGGCGTCGCTCTCTATATGGGAGCGTGGATTGAAATGGTATCAACGCCAAGATCGTTCATCAACGATTTAACGTCGCTCTCTATATGGGAGCGTGGATTGAAATAAAGGTACCAACGGCCAGAATGCTGCCTTTTCGTGTCGCTCTCTATATGGGAGCGTGGATTGAAATTTGAAATCTTGATACTCTACTCCGGCGGCCTTATGTCGCTCTCTATATGGGAGCGTGGATTGAAATACCGACCTTTGCGATGTCGGATGCTGATTGAGGCGTCGCTCTCTATATGGGAGCGTGGATTGAAATAATACGGTTATGAGATTGCTATCTATAGAACCTCGTCGCTCTCTATATGGGAGCGTGGATTGAAATGGCGGGATGGCCCAGGATATTAACAACTGGTCGAAGTCGCTCTCTATATGGGAGCGTGGATTGAAATGATTACGTCCAGCCGATTCGCATCATCTACTTTGGGTCGCTCTCTATATGGGAGCGTGGATTGAAATTATCACACCGGGAACGGTTTGAATTTAGAGTATATGTCGCTCTCTATATGGGAGCGTGGATTGAAATCAGGAACGAAGGAGTATGCAGATTATCAGAAGCGCGTCGCTCTCTATATGGGAGCGTGGATTGAAATCCGCTGATTGGGTAAGGTACTTTTTATCAAATGATGGTCGCTCTCTATATGGGAGCGTGGATTGAAATCTCTTTGGAGGGCTTATTTGTGGCTCCTATGCTGTTGTCGCTCTCTATATGGGAGCGTGGATTGAAATCACCAGGGACGCCAGGAAGGCCGTCCGCACCTGGGGTCGCTCTCTATATGGGAGCGTGGATTGAAATACTGGGAGTGTTGCACCATTTGGTTATAGAAAAAGTCGCTCTTTATGTGGGAGCGTGGATTGAAATCACTACCTGCTGCTCATTGAGCATCCGGGGGATTGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATAGGTTGTCGGTGACGTTACGGTCAAAGATGACTTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATGACCTTCCAGGCGCCGCCGTCTGCCTCGATCAGGGGGCGCTCCCTATATGGGAGCGTGGATTGAAATATAATGCGGCTACAGTCACCCGAGGCGACAAAGGGTCGCTCTCTATATGGGAGCGTGGATTGAAATAGTTGATGATCGAGGAACAGCATTTACCAGTATCAAGTCGCTCTCTATATGGGAGCGTGGATTGAAATTTGGCAGCATTAACATATCCACGATTAGCACTTGTGTCGCTCCCTATGTGGGAGCGTGGATTGAAATCCTCCTGGAGTTTCGCTTGATATTCCAAATCACGTCGCTCCATATATGGGAGCATGGATTGAAATCAAGGCAAGCGCTATCGCCTTGGTAAACGGGTTGATAGTCGCTCCCTCTATGGGAGCGTGGATTGAAATCGTTTGAGCTCGGCGTTGCTCCATTCCTTTACTTGGTCGCTCCCCATGCAGGAGATAGATTGAACTA

>NZ_LN831776|22|2|1603409-1605239|PILER-CR
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ATTTCCAAGGCTACCATACATCCCAAAATCAGTAA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ACCAATCTTGATAAAGATCAGAAATACAAACTTG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	TGTGATCCGGGAGCAGGGCGCTTTGTGTTCAGC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CCTATCGGGCAAAATTGTAGGCCCGGATGCTGCCA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CAATGGACGAATTAGAGCTTCTGCTAGAAAAAT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ATTTTACTACCATCCTTTCCCATGAAGTATGTTA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	GCCCTCTATTGGGCCGGCTTAGATGAAGAAGAGGAA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CTGTATACTCTCGAACAAAATTATTGATGCTAT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CACAACGATTCAATCTTTTGGTTGATCTCCCCGGC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	GGTATCAACGCCAAGATCGTTCATCAACGATTTAAC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	AAAGGTACCAACGGCCAGAATGCTGCCTTTTCGT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	TTGAAATCTTGATACTCTACTCCGGCGGCCTTAT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ACCGACCTTTGCGATGTCGGATGCTGATTGAGGC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	AATACGGTTATGAGATTGCTATCTATAGAACCTC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	GGCGGGATGGCCCAGGATATTAACAACTGGTCGAA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	GATTACGTCCAGCCGATTCGCATCATCTACTTTGG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	TATCACACCGGGAACGGTTTGAATTTAGAGTATAT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CAGGAACGAAGGAGTATGCAGATTATCAGAAGCGC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CCGCTGATTGGGTAAGGTACTTTTTATCAAATGATG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CTCTTTGGAGGGCTTATTTGTGGCTCCTATGCTGTT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CACCAGGGACGCCAGGAAGGCCGTCCGCACCTGGG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ACTGGGAGTGTTGCACCATTTGGTTATAGAAAAA
GTCGCTCTTTATGTGGGAGCGTGGATTGAAAT	CACTACCTGCTGCTCATTGAGCATCCGGGGGATTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGGTTGTCGGTGACGTTACGGTCAAAGATGACTT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GACCTTCCAGGCGCCGCCGTCTGCCTCGATCAGGG
GGCGCTCCCTATATGGGAGCGTGGATTGAAAT	ATAATGCGGCTACAGTCACCCGAGGCGACAAAGG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	AGTTGATGATCGAGGAACAGCATTTACCAGTATCAA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT

>NZ_LN831776|22|22|1603409-1605440|CRISPRCasFinder
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ATTTCCAAGGCTACCATACATCCCAAAATCAGTAA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ACCAATCTTGATAAAGATCAGAAATACAAACTTG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	TGTGATCCGGGAGCAGGGCGCTTTGTGTTCAGC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CCTATCGGGCAAAATTGTAGGCCCGGATGCTGCCA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CAATGGACGAATTAGAGCTTCTGCTAGAAAAAT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ATTTTACTACCATCCTTTCCCATGAAGTATGTTA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	GCCCTCTATTGGGCCGGCTTAGATGAAGAAGAGGAA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CTGTATACTCTCGAACAAAATTATTGATGCTAT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CACAACGATTCAATCTTTTGGTTGATCTCCCCGGC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	GGTATCAACGCCAAGATCGTTCATCAACGATTTAAC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	AAAGGTACCAACGGCCAGAATGCTGCCTTTTCGT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	TTGAAATCTTGATACTCTACTCCGGCGGCCTTAT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ACCGACCTTTGCGATGTCGGATGCTGATTGAGGC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	AATACGGTTATGAGATTGCTATCTATAGAACCTC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	GGCGGGATGGCCCAGGATATTAACAACTGGTCGAA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	GATTACGTCCAGCCGATTCGCATCATCTACTTTGG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	TATCACACCGGGAACGGTTTGAATTTAGAGTATAT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CAGGAACGAAGGAGTATGCAGATTATCAGAAGCGC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CCGCTGATTGGGTAAGGTACTTTTTATCAAATGATG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CTCTTTGGAGGGCTTATTTGTGGCTCCTATGCTGTT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CACCAGGGACGCCAGGAAGGCCGTCCGCACCTGGG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ACTGGGAGTGTTGCACCATTTGGTTATAGAAAAA
GTCGCTCTTTATGTGGGAGCGTGGATTGAAAT	CACTACCTGCTGCTCATTGAGCATCCGGGGGATTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGGTTGTCGGTGACGTTACGGTCAAAGATGACTT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GACCTTCCAGGCGCCGCCGTCTGCCTCGATCAGGG
GGCGCTCCCTATATGGGAGCGTGGATTGAAAT	ATAATGCGGCTACAGTCACCCGAGGCGACAAAGG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	AGTTGATGATCGAGGAACAGCATTTACCAGTATCAA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	TTGGCAGCATTAACATATCCACGATTAGCACTTGT
GTCGCTCCCTATGTGGGAGCGTGGATTGAAAT	CCTCCTGGAGTTTCGCTTGATATTCCAAATCAC
GTCGCTCCATATATGGGAGCATGGATTGAAAT	CAAGGCAAGCGCTATCGCCTTGGTAAACGGGTTGATA
GTCGCTCCCTCTATGGGAGCGTGGATTGAAAT

>NZ_LN831776|22|2|1603409-1605507|CRT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ATTTCCAAGGCTACCATACATCCCAAAATCAGTAA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ACCAATCTTGATAAAGATCAGAAATACAAACTTG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	TGTGATCCGGGAGCAGGGCGCTTTGTGTTCAGC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CCTATCGGGCAAAATTGTAGGCCCGGATGCTGCCA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CAATGGACGAATTAGAGCTTCTGCTAGAAAAAT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ATTTTACTACCATCCTTTCCCATGAAGTATGTTA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	GCCCTCTATTGGGCCGGCTTAGATGAAGAAGAGGAA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CTGTATACTCTCGAACAAAATTATTGATGCTAT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CACAACGATTCAATCTTTTGGTTGATCTCCCCGGC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	GGTATCAACGCCAAGATCGTTCATCAACGATTTAAC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	AAAGGTACCAACGGCCAGAATGCTGCCTTTTCGT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	TTGAAATCTTGATACTCTACTCCGGCGGCCTTAT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ACCGACCTTTGCGATGTCGGATGCTGATTGAGGC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	AATACGGTTATGAGATTGCTATCTATAGAACCTC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	GGCGGGATGGCCCAGGATATTAACAACTGGTCGAA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	GATTACGTCCAGCCGATTCGCATCATCTACTTTGG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	TATCACACCGGGAACGGTTTGAATTTAGAGTATAT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CAGGAACGAAGGAGTATGCAGATTATCAGAAGCGC
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CCGCTGATTGGGTAAGGTACTTTTTATCAAATGATG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CTCTTTGGAGGGCTTATTTGTGGCTCCTATGCTGTT
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	CACCAGGGACGCCAGGAAGGCCGTCCGCACCTGGG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	ACTGGGAGTGTTGCACCATTTGGTTATAGAAAAA
GTCGCTCTTTATGTGGGAGCGTGGATTGAAAT	CACTACCTGCTGCTCATTGAGCATCCGGGGGATTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGGTTGTCGGTGACGTTACGGTCAAAGATGACTT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GACCTTCCAGGCGCCGCCGTCTGCCTCGATCAGGG
GGCGCTCCCTATATGGGAGCGTGGATTGAAAT	ATAATGCGGCTACAGTCACCCGAGGCGACAAAGG
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	AGTTGATGATCGAGGAACAGCATTTACCAGTATCAA
GTCGCTCTCTATATGGGAGCGTGGATTGAAAT	TTGGCAGCATTAACATATCCACGATTAGCACTTGT
GTCGCTCCCTATGTGGGAGCGTGGATTGAAAT	CCTCCTGGAGTTTCGCTTGATATTCCAAATCAC
GTCGCTCCATATATGGGAGCATGGATTGAAAT	CAAGGCAAGCGCTATCGCCTTGGTAAACGGGTTGATA
GTCGCTCCCTCTATGGGAGCGTGGATTGAAAT	CGTTTGAGCTCGGCGTTGCTCCATTCCTTTACTTG
GTCGCTCCCCATGCAGGAGATAGATTGAACTA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_046501633.1|1618215_1619322_-|linear-amide-C-N-hydrolase	unknown	unknown	gnl|CDD|367486
NZ_LN831776.1|WP_020431435.1|1600719_1601094_+|type-III-B-CRISPR-module-associated-protein-Cmr5	cmr5gr11	COG3337_cmr5gr11_CAS-III-B	gnl|CDD|378242
NZ_LN831776.1|WP_020431504.1|1610922_1611783_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	COG3649_cas7_CAS-I-C	gnl|CDD|187820
NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	gnl|CDD|273847
NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	gnl|CDD|187887
NZ_LN831776.1|WP_020431433.1|1598495_1599794_+|type-III-B-CRISPR-module-associated-protein-Cmr3	cmr3gr5	pfam09700_cmr3gr5_CAS-III-B	gnl|CDD|370625
NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	gnl|CDD|224124
NZ_LN831776.1|WP_046501621.1|1590447_1592427_+|TetM/TetW/TetO/TetS-family-tetracycline-resistance-ribosomal-protection-protein	unknown	unknown	gnl|CDD|223556
NZ_LN831776.1|WP_020431498.1|1613466_1613757_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl|CDD|187856
NZ_LN831776.1|WP_020431500.1|1612425_1613457_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	gnl|CDD|188360
NZ_LN831776.1|WP_020426229.1|1622135_1623242_+|GGDEF-domain-containing-protein	unknown	unknown	gnl|CDD|143635
NZ_LN831776.1|WP_020431436.1|1601115_1601931_+|type-III-B-CRISPR-module-RAMP-protein-Cmr6	cmr6gr7	COG1604_cmr6gr7_CAS-III-B	gnl|CDD|224520
NZ_LN831776.1|WP_020431502.1|1611772_1612429_+|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl|CDD|224385
NZ_LN831776.1|WP_020427482.1|1588762_1589755_-|S-layer-homology-domain-containing-protein	unknown	unknown	gnl|CDD|306825
NZ_LN831776.1|WP_046501630.1|1617329_1618190_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|197666
NZ_LN831776.1|WP_052741421.1|1601927_1602917_+|hypothetical-protein	PD-DExK	mkCas0090_PD-DExK_CAS-I:CAS-III	unknown
NZ_LN831776.1|WP_020431432.1|1596667_1598527_+|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	cas10	cls000742_cas10_CAS-III	gnl|CDD|274208
NZ_LN831776.1|WP_020431434.1|1599790_1600720_+|type-III-B-CRISPR-module-RAMP-protein-Cmr4	cmr4gr7	cd09682_cmr4gr7_CAS-III-B	gnl|CDD|274210
NZ_LN831776.1|WP_167345589.1|1595246_1596710_+|type-III-B-CRISPR-module-RAMP-protein-Cmr1	cmr1gr7	COG1367_cmr1gr7_CAS-III-B	gnl|CDD|224286
NZ_LN831776.1|WP_046501615.1|1587521_1588331_+|hypothetical-protein	unknown	unknown	gnl|CDD|237030

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831776.1|WP_020431435.1|1600719_1601094_+|type-III-B-CRISPR-module-associated-protein-Cmr5	cmr5gr11	COG3337_cmr5gr11_CAS-III-B	4.9e-21	69.9	0.0
NZ_LN831776.1|WP_020431504.1|1610922_1611783_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	COG3649_cas7_CAS-I-C	2.3e-127	418.8	0.8
NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	1e-60	199.7	0.0
NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	7.7e-161	531.0	1.6
NZ_LN831776.1|WP_020431433.1|1598495_1599794_+|type-III-B-CRISPR-module-associated-protein-Cmr3	cmr3gr5	pfam09700_cmr3gr5_CAS-III-B	1.3e-72	240.0	0.0
NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	3.3e-85	281.5	7.6
NZ_LN831776.1|WP_020431432.1|1596667_1598527_+|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	cas10	cls000742_cas10_CAS-III	1.2e-78	259.7	4.1
NZ_LN831776.1|WP_020431498.1|1613466_1613757_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	1.1e-31	103.6	1.1
NZ_LN831776.1|WP_020431500.1|1612425_1613457_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	3.4e-146	481.3	0.2
NZ_LN831776.1|WP_020431436.1|1601115_1601931_+|type-III-B-CRISPR-module-RAMP-protein-Cmr6	cmr6gr7	COG1604_cmr6gr7_CAS-III-B	1.3e-50	167.1	0.0
NZ_LN831776.1|WP_020431502.1|1611772_1612429_+|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	9.6e-35	114.8	1.6
NZ_LN831776.1|WP_052741421.1|1601927_1602917_+|hypothetical-protein	PD-DExK	mkCas0090_PD-DExK_CAS-I:CAS-III	8.9e-27	87.9	0.3
NZ_LN831776.1|WP_020431434.1|1599790_1600720_+|type-III-B-CRISPR-module-RAMP-protein-Cmr4	cmr4gr7	cd09682_cmr4gr7_CAS-III-B	1.9e-74	245.5	0.0
NZ_LN831776.1|WP_167345589.1|1595246_1596710_+|type-III-B-CRISPR-module-RAMP-protein-Cmr1	cmr1gr7	COG1367_cmr1gr7_CAS-III-B	1.7e-65	216.2	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_046501633.1|1618215_1619322_-|linear-amide-C-N-hydrolase	gnl|CDD|367486	pfam03417, AAT, Acyl-coenzyme A:6-aminopenicillanic acid acyl-transferase.	1.24319e-30
NZ_LN831776.1|WP_020431435.1|1600719_1601094_+|type-III-B-CRISPR-module-associated-protein-Cmr5	gnl|CDD|378242	pfam09701, Cas_Cmr5, CRISPR-associated protein (Cas_Cmr5). CRISPR is a term for Clustered, Regularly Interspaced Short Palindromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This family, represented by TM1791.1 of Thermotoga maritima, is found in both archaeal and bacterial species.	2.24088e-19
NZ_LN831776.1|WP_020431504.1|1610922_1611783_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	gnl|CDD|187820	cd09689, Cas7_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas7. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas7 is a RAMP superfamily protein; Subunit of the Cascade complex; also known as Csd2 family.	9.02891e-134
NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5	gnl|CDD|273847	TIGR01876, cas_Cas5d, CRISPR-associated protein Cas5, subtype I-C/DVULG. CRISPR is a term for Clustered, Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This small Cas family is represented by CT1134 of Chlorobium tepidum. This family belongs to a set of several Cas protein families, one each for a number of different CRISPR/Cas subtypes, that share a region of N-terminal sequence similarity modeled by TIGR02593. This family represents the Dvulg subtype of CRISPR/Cas locus.	3.09357e-90
NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	gnl|CDD|187887	cd09757, Cas8c_I-C, CRISPR/Cas system-associated protein Cas8c. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Zn-finger domain containing protein, distant homologs of Cas8 proteins; signature gene for I-C subtype; also known as Csd1 family.	2.89947e-169
NZ_LN831776.1|WP_020431433.1|1598495_1599794_+|type-III-B-CRISPR-module-associated-protein-Cmr3	gnl|CDD|370625	pfam09700, Cas_Cmr3, CRISPR-associated protein (Cas_Cmr3). CRISPR is a term for Clustered Regularly Interspaced Short Palindromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR associated) proteins. This highly divergent family, found in at least ten different archaeal and bacterial species, is represented by TM1793 from Thermotoga maritima.	9.36311e-74
NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3	gnl|CDD|224124	COG1203, COG1203, CRISPR-associated helicase Cas3 [Defense mechanisms].	7.24875e-69
NZ_LN831776.1|WP_046501621.1|1590447_1592427_+|TetM/TetW/TetO/TetS-family-tetracycline-resistance-ribosomal-protection-protein	gnl|CDD|223556	COG0480, FusA, Translation elongation factors (GTPases) [Translation, ribosomal structure and biogenesis].	1.92368e-170
NZ_LN831776.1|WP_020431498.1|1613466_1613757_+|CRISPR-associated-endonuclease-Cas2	gnl|CDD|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	1.93294e-34
NZ_LN831776.1|WP_020431500.1|1612425_1613457_+|type-I-C-CRISPR-associated-endonuclease-Cas1	gnl|CDD|188360	TIGR03640, cas1_DVULG, CRISPR-associated endonuclease Cas1, subtype I-C/DVULG. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes the Cas1 protein particular to the DVULG subtype of CRISPR/Cas system.	0
NZ_LN831776.1|WP_020426229.1|1622135_1623242_+|GGDEF-domain-containing-protein	gnl|CDD|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	2.76115e-51
NZ_LN831776.1|WP_020431436.1|1601115_1601931_+|type-III-B-CRISPR-module-RAMP-protein-Cmr6	gnl|CDD|224520	COG1604, COG1604, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	6.42086e-57
NZ_LN831776.1|WP_020431502.1|1611772_1612429_+|CRISPR-associated-protein-Cas4	gnl|CDD|224385	COG1468, COG1468, CRISPR-associated protein Cas4 (RecB family exonuclease) [Defense mechanisms].	1.41191e-27
NZ_LN831776.1|WP_020427482.1|1588762_1589755_-|S-layer-homology-domain-containing-protein	gnl|CDD|306825	pfam00395, SLH, S-layer homology domain.	9.58091e-06
NZ_LN831776.1|WP_046501630.1|1617329_1618190_-|helix-turn-helix-domain-containing-protein	gnl|CDD|197666	smart00342, HTH_ARAC, helix_turn_helix, arabinose operon control protein.	5.79213e-25
NZ_LN831776.1|WP_020431432.1|1596667_1598527_+|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	gnl|CDD|274208	TIGR02577, thermophile-specific_DNA_repair_system, CRISPR-associated protein Cas10/Cmr2, subtype III-B. This model represent a Crm2 family of the CRISPR-associated RAMP module, a set of six genes recurring found together in prokaryotic genomes. This gene cluster is found only in species with CRISPR repeats, usually near the repeats themselves. Because most of the six (but not this family) contain RAMP domains, and because its appearance in a genome appears to depend on other CRISPR-associated Cas genes, the set is designated the CRISPR RAMP module. This protein, typified by TM1794 from Thermotoga maritima, is designated Crm2, for CRISPR RAMP Module protein 2.	1.72839e-72
NZ_LN831776.1|WP_020431434.1|1599790_1600720_+|type-III-B-CRISPR-module-RAMP-protein-Cmr4	gnl|CDD|274210	TIGR02580, putative_CRISPR-associated_protein, CRISPR type III-B/RAMP module RAMP protein Cmr4. This model represents a CRISPR-associated protein from the family that includes TM1792 of Thermotoga maritima. This family is part of the broad RAMP superfamily (pfam03787) collection of CRISPR-associated proteins. It is the fourth of a recurring set of six proteins, four of are in the RAMP superfamily, that we designate the CRISPR RAMP module.	6.03973e-78
NZ_LN831776.1|WP_167345589.1|1595246_1596710_+|type-III-B-CRISPR-module-RAMP-protein-Cmr1	gnl|CDD|224286	COG1367, COG1367, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	1.88045e-53
NZ_LN831776.1|WP_046501615.1|1587521_1588331_+|hypothetical-protein	gnl|CDD|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	1.69539e-09

Protein sequences

>NZ_LN831776.1|WP_052741421.1|1601927_1602917_+|hypothetical-protein
MKDKQPSSEQELEEMRKAAPKIIQQIAQNYIHLEESITSQLRMAAGSHHVTSGTFREDIWKSLFEQIIPRKFSIEQSVFIIDSHGLVSKEVDLAIFDEQYTPYIFRLGRIKYIPIEAVAVVVQCKSNNIHGRNKRENLRTWSKSITNLKTSLKSVARIHTGIAKGEYDYILDKDGQLRIEPEKLEKSDRDKLAQTSTRPIQILCHTKDTSSSKYDDLFDIVIHPEGERLRVEMKPDLKDLPSWYDSLNHKQDPRYEHIVKPFDTKEPSEDFQKALQVDNYKVYKDKARTKEIGLLSLTFQLNQLLMLINNPILFPHMAYVDMFNTNISK
>NZ_LN831776.1|WP_020431436.1|1601115_1601931_+|type-III-B-CRISPR-module-RAMP-protein-Cmr6
MNAYLAITKQEASNKGSKLYRVVNGDLQNTKGEFYRQLIKEYQADWKQSCIWYEQRYEHYSTKLHDTLGDSRCIEFEMASISPLLIGHGGVSALETSLMLHRIYGVPYIPGSAIKGVTANYCHCMLGAENPAFLSDGEYYEALFGSQDQAGYINYEDAWVTPATAESALIDDVMTPHHQNYNSIQLQRTDQQKASAPRDDDDPVPLPFLAVNASFRFLLTCPSDRVEKEDARQWLNIAQEIVSHALQYEGIGGKTNAGYGRMLQADRRERE
>NZ_LN831776.1|WP_020431435.1|1600719_1601094_+|type-III-B-CRISPR-module-associated-protein-Cmr5
MKSAAHTYAEKAMQSIRSVEADPDCNNKDYGRLCLLFPSMVQVNGLRLTVAFFQSKGKSQKTLHQRYLQDLAAAVGSAAWETGLSTNDMMDYRDLTRHVLQAAVWFKRYAEAILKVEAADGLDS
>NZ_LN831776.1|WP_020431434.1|1599790_1600720_+|type-III-B-CRISPR-module-RAMP-protein-Cmr4
MTNNRLYYVHCMSSVHIGTGQGVGIIDMPMIREKVTEWPYLPGSSMKGVHRVFFKSGIHKQPEKWLNSAFGKASNKGTNFNSDDGFELDDGNAGALVMSDAKILAFPVASRYGTFAYVTCPLVLKRFRRDTVAAGVDMPEFDWAALESVVNSGVVMLHTDSKLDKNNEVFVDEFTSGAVKDEAFAKWTDWLAGQIFVKDELSETMLKERMLLVSDEAFQYFVSMCSEVVPRIRIGLETGSVEPGALWNEEYLPVESILYGVIWSDGISVKTLENRGLLDIFPEEAFLQIGGNATVGKGRIRCRYVKGGA
>NZ_LN831776.1|WP_020431433.1|1598495_1599794_+|type-III-B-CRISPR-module-associated-protein-Cmr3
MERTIQIQPLDPLMIRDGRPFGNTPGARAHTLGTVTPGVVAGTLRTLMQKNNTAGTFGTTTKDAEREGKPSTVAKVDIRGPLYMLNDRLFLPMPYDLDLYEPGLQEDPASIHVNVRRPIEPAKNTPTHLHGFLGTGKTSLHEDKLWPVSMDTEIRKPLKSAPAYISAEWMIKWLCDNLQPEQWSAAIAEWRSKPEDKVHFIAPFVKEVRTHTAIQAETSTVQDKALFSTESLVIPPDVSLIASASIGSDVKWEGTISGIHSFGGKRRLAHFREIDDQEIQDNIWKCPEAIAQAVAENPRYLRMVLATSAYFSKGWLPGWLDGDLRSTDRFDKQLQIELCWACLPRWEGISGWSYRHNQPKAVRRMVAAGSVYFFKVISGDPVEFVRRNWLTSMSDEDRRKAFFDKQDGYGLATWGVWTPYGHHKGMDKGDIR
>NZ_LN831776.1|WP_020431432.1|1596667_1598527_+|type-III-B-CRISPR-associated-protein-Cas10/Cmr2
MEENFLQAEPQTEVVMLISIGPVQEFIAQARKTRDLWFGSHLLSEISKEAARRLAEAHNARMIFPYIHKEKIAYGLDDLKVANKVLAIVPTNDPKAVALDVRRAVVTKWLGYANKAKEELGSGIIGPMWERQVKDFIEFYAVWSELESEEKYAEVLQQTEQLMAARKTLRDFRPNEPADLFGDDKSGLDSGRESVLKPSQYMSYAGFGIKHKETLDAISLVKRLSRFTVDKKEFKSVCDVAFQQFRDELGASRNQWMKTAVDEYYRDLKHKYGTALKLTGSDLQSYKSEMFYTSRVEEAVVELAAEMKKPINRVKQLEITQNILTSLEELYGKILKEPTPYYALVVGDGDRMGDALRKMKTPAEHQSFTEHLSGFASEVERIVFKDDIKGQMIYSGGDDLMALLPVHRCLAAAQEIRQAFTNTMTLALPDEDQRPTLSVGIAIVHMFEPLEDSLLIARAAEALAKVRRDELAIHFQKRSGSEEMRVSLPFSENPVNTIVKLQSLYRNRYISTSFAYGLRQLHAEYLDLKAHGSLQNEGMGELLYFEIRRLLLLKKPEFKSKDEIIKEVLSVFKGLEQTDSDRVKDPLVLLNRLAEQCVIAVTLEKVGGAYGTNDTNSTS
>NZ_LN831776.1|WP_167345589.1|1595246_1596710_+|type-III-B-CRISPR-module-RAMP-protein-Cmr1
MDPKKEIKPPTLDLVIKDIQESRKKVPEDRFNITIVTPMFGGGSKPGFTDSAFPIRSASIRGHLRFWWRATRGAAFESVTELRQREVEIFGDSHSPSRVKISVHIFNKTEPEKGKEHSASINNETPKRTVRLPRYAVFPFDKNNPGSNMQQFELTIRYTPRLPKQADTLENGSKPFLNVEQLRKEITPALWAWINFGGLGSRTRRGCGSLYCKDFAPERTSTHPKYEDWFHGKVADYELELDTQLEKKEWPTLSRSVIIQEYERDMISAWNDVIKLYHNFRSQPNNTYIYSKPPKYERSLWPEADSLRRVTGMSEEDHKKPSPFKKQEFFSFPRAQLGLPIIFQFKQDEYLKKRYSNFREPYNMQLAPKDKSRLASPLITKALARSDKRGVGIIVKLNQPRLSELELKVIENKEDKRKRSPRDFAHIESIEELVAHKPIREKDIYKELSYPGSPMKQGQKSAIQAFLESEEVKEWKRTSYRPNPKQK
>NZ_LN831776.1|WP_046501621.1|1590447_1592427_+|TetM/TetW/TetO/TetS-family-tetracycline-resistance-ribosomal-protection-protein
MVQQQGMERINVGIFAHVDAGKTTTTEHILYESGRIKAVDSVDSGTALTDSMEVERQRGISVRAALASFEWRGVQVNLVDTPGHVDFLSEVERSLRVMDCAVLILSAVEGVQAQSEMIWNALRKLGIPTLVFLNKMDRTGADPEAVLVQARTYLSGDILPVQQALGQEQEYAGAVDLWAEAADPAARIELLEALAERDEALLETYMSDTPLDLTAWKEQLKAGAAAGRWFPLVYGVAAKGLGITQLLDAMTDYFPRAGGNPQLPVSGIVYSIQRDKTMGRMAYVRLYQGMVRNRDTVMNYTQDVQGKVTQIRKVEGGRTEDVGTLEAGDIAVVYGLSGVKIGDVLGVPDAVPQEAKLAVPLLTVRVHWDAAVDEHKVIGAFQELADEDPLLDTQWLQDERELHIKVMGPIQLEILDSVLESRYGLKVTFGQPSVIYRETPSRAGEGYVAYLMPKPCWAILRFRIEPGPPGSGLRYESLVRSSDLLPQYQNETARRVPEALMQGLYGWEVTDLKVTLTEGQHHVWHTHPLDFAVATPMAIMDGLNRVGTKLLEPILQVRIVVPEENGGRVMNDLVQMRGTFEPPVLQGERMIIEGRLPLATSLDYPVSLSSYTKGRSTFTSFFAGYEECPPDVRAERTRRGVNPLDQARYILSVRKALQG
>NZ_LN831776.1|WP_020427482.1|1588762_1589755_-|S-layer-homology-domain-containing-protein
MNKYSFQMSAKKITIACGILAASVSFGASAFAFSDIKGDPAESKINALHNKGVVNGVTTDRFAPKSKVTFAQGIQFIVNGLQLSPKASGGGSTVTSSVYFDKVKDKAWYASAFLIAKQNGLTLDKSVDPNAAMTRIQFAHLLTQALQSKGNFPVTLMYADISDGSKLSNAEMNSLQILVNTHLVTLEKNNTFRPNDAVTRAEAAVWIYDAAEFAQTVITPEVTPPDEGTAAPAQLYEGSITLEKAGQGVNKVTLTVNDLPNPGYGLAINRIEFGKDKTAVIYFSVTKPDPGKMYPMVITKGTAVTYLPEGYTATAKSLTAAPSSSGSSVR
>NZ_LN831776.1|WP_046501615.1|1587521_1588331_+|hypothetical-protein
MITVKKILGHSALAALLLVLAACNSASEAEPQQTQGSPSPSASASAAPSASASAAPSASASAAPSTSASAVPSAPASAAPASSEPAESQVPQASGAPEEGTPPTAMEAATTVLRALSRGNMETLASWAHPDKGVRFSPYAHVDTATDLVFTRDQLEGLMKDSKPYVWGKFAGSGEAIKLTFAEYFKRFVYDADFMNKAETALNKGLGQGTTLNNINEVYPKDSYDFVEYHIAGVDPANEGMDWRSLRLVFEKMGEDRALVGIVHDQWTP
>NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3
MEYIAHIRESDMKVQTVTEHLLEVRTLAEKYGKKLGIKYMAGLAGMLHDLGKYTEEFRNYIVQAVYHPEAPPSRGSVDHSTAGGKLLFERFHRVPADLSNKEAHINKMILAEVVGNAILSHHSYLQDFLNPDSESNFLNRVQDKCLPEFERAKDSFFELVMNETEFHLYVDKAVEELSDYLKVDSSSTTELKLMFLTKYVFSALIDADRTNTRCFEENQPDPSYNPQQLFSAYYTKLMTKIDSFHNHKHAHSAINQLRQGMSEQCEQFAAEPSGIYTLSIPTGGGKTLASLRYALKHALLKEKKHIIYVVPYTTIIEQNANEIRSILKDDEHILEHHSNVVEEETQDDEHEDGSLSLRQKLKLAKDNWDAPIIFTTMVQFLNVFYADGSRNIRRLHNLSESVIVFDEVQKVPVRCVSLFNQALNFLKSYAHSSIVLCTATQPELDYVRLKLEIEPEAEMIHNLDHVIEAFRRVEIVDRATNEHFDNDTLTEFVITQMREVSSVLVILNTKSVVQALYRSLNERNLSVPIYHLSTSMCAAHRNQILDKVKALLEDKEPVICISTQLIEAGVDVSFQCVIRSLAGLDSIAQAAGRCNRHGEDLIRQVYVIDHIEENLKHLKEIKIGKEISRKILIDLSRDASLHGGHILSIQAMEKYFKEFYTELATSLNYSIPKLGQEMTTLLSGPRKNNAYYQAYLSKHRAALPLFLLNSYKTAAENFQVIDNLTTTVVVPFGDGPEEGKDIIAELNGQQSIPDLTRLLRKAQQYTINIYSYEKDLLSKNGSLVPYLDGKILALKEGAYHPEYGLNLENDSPLDMYMF
>NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5
MRNSIEFKVYGKYALFTDPLTKLGGEKLTYSVPTYQALKGIVESIYWKPTIHIIVEEVRIMNAIRMESKGIRPMDYGGGNTLANYTYLKDVCYEVRAHFEFNMNRPDLEHDRNEHKHHNLLKRSLQAGGRRDIFLGARECQAYVEPCVFGVERGFYNDYGDIHLGSMVHGINYPDETGRDEMEVRLWSPVMRDGIIRFIRPEECTQVRRIAEMKPKSFNETNLQTAEELLAQIEAEEKA
>NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1
MSWLLNLYETYQSNQDCVGVIETRYNDREYTLLPVSHTTQNAHIEVNVTEDGEFHSASVLDKSESSTLIPCTEDSASRAGSKVAPYPLHDKLSYVAGDFLAYGGKIKKEEPFAAYIKQLGGWADSPYACPKVKSIHSYLSKRRLIQDLVSHSILFLDADHQLIEKWDKKYEALHGEKPLIFSAVAGEQESAFIRFNVYSPDKELTKVWKDPEMYDSFMQYYSHLLGQEDYCYVTGRMLPSTDRHANKIRNAADKAKLISSNDTSGFTFRGRFTQSSDAASISYEVSQKAHNALKWLINRQGKIVDQRVFLVWGNDDLNIPDPTEDFFSFDLEPAVARERKSYTHKEYAGEIAKAMDGYRNKLASEYKSDVNILVLDSATTGRLAVLYYRNMDKQLYLDKLVHWHSTCSWLHRYRKNTQDEWVEFYGASATKDIAFAAYGPKANEKIVKGVMERLLPCIVDGHNIPQDIVRSAFYRASNPVSMEKWEWEKTLSITCALINAKEEMNVALDTEIDDRSYLFGRLLAIADVLERRALDSDEKRSTNAIRYMNAFSQHPERTWNTIQQSIQPHQARLGTKLRYYSSLIDEVASKIPLDQFNNKPLSGKYLLGFYSQRHELYQKKDKNNDSIQASENGER
>NZ_LN831776.1|WP_020431504.1|1610922_1611783_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2
MTILDHKIDFAVIVSVTKANPNGDPLNGNRPRQNYDGYGEISDVALKRKIRNRLQDMGESIFVQSNDRKSDSYNSLRERADANAELDKILKAKGSSNEEFARIACQEWLDVRSFGQVFAFKADKGAGVSVGVRGPVSIHTATSVSPIDITSMQITKSVNSEPGKDRGSDTMGMKHRVDFGVYVFYGSINTQLAEKTGFSNEDAEKIKQVLVTLFENDASAARPDGSMEVHKVYWWEHNSKLGQYSSAKVHRSLVVRPKVDDPKTIADYEIVVSEMEGLKAEVIDGI
>NZ_LN831776.1|WP_020431502.1|1611772_1612429_+|CRISPR-associated-protein-Cas4
MEYDDEDELMLSGIQHFHFCKRQWALIHIEQQWEENVRTIEGQHLHRNADQPLIREKRVDKIIVRAMPVKSRELNISGICDVVEFIRDDSGVEINGADGKYAAYPVEYKRGKPKREDEDILQLAAQAMCLEEMLLCEVSTGYIFYNEIKHRIEVPLTAELKANVKAIVEVMQSYYHRRHTPKVKTGPFCKSCSLQHICLPKLMNKQSVKSYVEGKIRE
>NZ_LN831776.1|WP_020431500.1|1612425_1613457_+|type-I-C-CRISPR-associated-endonuclease-Cas1
MKKLLNTLYITQPSVYLSLDGDNVVLLKEEEKLGRFPLHNLESIVTFGYTGASPALMGYCADSNISLLFLTMNGRYLARVTGQSRGNVVLRKKQYNLSEDEVRSAKIARNFIIGKIYNHKWMLERMTRDYPLRVNVELFKETSQQLSSLILEVRACEQLDRLRGLEGQAAATYYSQFNQMILQQKEDFYFHSRTRRPPLDNVNAMLSLAYTLLTHDTASALEAVGLDAYVGFLHRDRPGRVSLALDVMEELRGVFADKFVLTLINKKLISKADFLKKENGAVIMTDEARKKFLAAWQSKKQETITHPYLGEKISWGLVPHAQALLLARHLRNDLDEYPPFLWK
>NZ_LN831776.1|WP_020431498.1|1613466_1613757_+|CRISPR-associated-endonuclease-Cas2
MLVVITYDVSTLSGEGQSRLRKVSKICQNYGQRVQNSVFECVVDAAQFAELKIKLKTIIDDDEDSIRFYQLGNNHKNKVEHVGIKKSIDLEGPLIL
>NZ_LN831776.1|WP_046501630.1|1617329_1618190_-|helix-turn-helix-domain-containing-protein
MINNRAIGEAIVFIENSLYEPIAACDVAKAVSYSYYHFHRYFQAIMGETIGSYIRTRRLTQAAWDLVHSEKKILDIGVSLYFETAESFTRAFKDRYGMTPTEYRKNGIDVLIGNRPPAQISDNIVHPYADLSPQIVTVPETYTMGIRFITTISRNESIAMWQLFNQQIPDTFAGTRYGIFEAGETCAADVFNPQSETTAFVGIEFPKEQPILRGMERKTIRGGKYARFIHKGIVKDLMQTYHYIWGVWFPKSGYELDNRDDFECYTERFAGENIESSEIDIYFPIK
>NZ_LN831776.1|WP_046501633.1|1618215_1619322_-|linear-amide-C-N-hydrolase
MEKTKVYFKNFIGTSYEVGTEIGQWVLSTPSLLKQVLLPPNAYPNDKFTKITDLLDRYCQGINEEIKGFADTIGVSSEQALFYTMTYLERGCSLMAVLPSKSKSGHTLMARNYDFNNEMEEMCFAFTNIKGKYRYIGSTLNLFGRCDGMNEHGLAVCKASNGVPVGNFEGGQKAGATGFSFWVVVRSILENCKTVQEAIEWTMSAPIGYNMNLMLADSSNKIALLQCMDGHKSYKLLDEYSEEAFLSVTNHAVLEDIKPYQKMIIENSVVRNNKIVEVFTGKKQLSKKDMKTLLSTSYPDGLCCHYYKEFFGTLRSMIFDVNDKTIEMTFGSPQVNEWQTFSVGALEMQEVEVLLPQEKARPDFYKIS
>NZ_LN831776.1|WP_020426229.1|1622135_1623242_+|GGDEF-domain-containing-protein
MSPSGTSAYRQAKWIKRFLQTYWLVIALHFLAQLAAYTFLPYERGAHEFYYGVLLYPTLLMGAVVGIAQWIDRRASKYSFISLFMAGTIIAMIIIHLNMDIRIIGALMLLPIFASAIFYRLDLTFFTFALQAVAFFVMYRWDYWFKYFFSSFDLIAIPIFLVVGTLVASIMIINGRELVSDLEASLMAKQDLLIENAVMRKLSTTDALTDLYNHISFHEFYDKALEYGDQGAPFHLALIDIDNFKLINDKYGHRAGDIILARVAKVIRDLISSADIAARYGGEEFAILFFEKTFEEAEAIADKIRLRLSGTPHEEMDGAAVTVSIGLKSYSQGTTKEQLFEEVDALLYAAKHEGKNKVRTPYSSTVFT

Crispr_ID: NZ_LN831776_23

• CRISPR_ID: NZ_LN831776_23
• CRISPR_location: 1613926-1617063
• CRISPR_type: TypeIII
• Repeat_type: NA:I-C
• Spacer_info: 47 spacers
• Cas_protein_info: cas2,cas1,cas4,cas7,cas8c,cas5,cas3,PD-DExK,cmr6gr7,cmr5gr11

Consensus repeat of NZ_LN831776_23

Consensus_repeat	Method
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	PILER-CR
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CRISPRCasFinder
GTCGCTCCTTANGTNGGAGCGTGGATTGAAATN	CRT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	PILER-CR
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CRISPRCasFinder

spacers of NZ_LN831776_23

>23.1|1613958|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
AAACGCTGCACTTAAAGACTTGGCAAAAGTGGAGT
>23.2|1614025|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
TCCATATGAAATGTACCGCGCATATGGTGTTTATGG
>23.3|1614093|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CCGTTGGCAATCGGCGCAGAAGCAAGGTCATTG
>23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ATCATGACGCGCTGGCACGAGGATGATTTAATC
>23.5|1614223|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
AAAGTCCGAGACGTCGAAATCATCGTTCTTGCT
>23.6|1614288|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CCGATTGAAGGAAACATCTGGGGAAAAGGATTTATG
>23.7|1614356|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ATGATGGATTGTACAAGGATAGCCGCCATGGTGAGT
>23.8|1614424|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CACTTATGGTACTACTGAAAAGGCGTTGAGTGGAA
>23.9|1614491|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ATTGCCAATGTCCTCTTGAAGCTTCTCATAGCGC
>23.10|1614557|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ACATGGCACCGTTTGTCCGGTGCTGTCTATGTGTA
>23.11|1614624|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
AGCATCATCCGCCCGTATCTTCTCTGCTTCACGC
>23.12|1614690|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ACCCCATCCATTTGTAACTATGGGCTGTGACATG
>23.13|1614756|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CTCAGTTAAATGTGGGTACTTTGTGAATAAGTCCTG
>23.14|1614824|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CGTCAACTATCACACACTCGCGTCAATCCGTCAC
>23.15|1614890|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ATTAGTTGAATAACCCCTTGACCTGATGTGCGATA
>23.16|1614957|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
AGCAGCAGTCTAATCATATAGATTTAGAGTATCC
>23.17|1615023|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
TCAGTTTCCGCAGCCTTTGCATTTTCGGCTTTAT
>23.18|1615089|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CACTGCCTAAGACGGAGCGAGCCGCAGCGAAAT
>23.19|1615154|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
ATAAACTCAACCTGTTTGACTCACACAGCTTTG
>23.20|1615219|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
CAGCACCCGATCAAAATCCAGTCCACCCAGGAGT
>23.21|1615285|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
GGAAGTAGAGAGCCTTACGAGCCACAAGACACACT
>23.22|1615352|32|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
GGCACGGGACAAACTGGATGATTTATTGCTGG
>23.23|1615416|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT
AGGCTTGCCTAATTGTAATAATTTGTCGTAAATA
>23.24|1615482|34|NZ_LN831776|CRISPRCasFinder,CRT
AAATTGCTATTAATAATGCAAATATTGCAGCAAG
>23.25|1615548|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
CTATCCGTGAAGACCTTTTCCCACGGCCCCCAAT
>23.26|1615614|36|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
AGGAGATCCGGATCAGCGCGCAGCTGCTTCGTATCT
>23.27|1615682|35|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
ACAATATTGGAATGCAAAACCTGTTTTCACATCCC
>23.28|1615749|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
TTGTTTGCAATTTAATTAATGAATACTTATGTAT
>23.29|1615815|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
TCTCATAACCAGAGATGGTACCATTAGAAACTCC
>23.30|1615881|33|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
TAAAATACAAAAACATTACCGAACCAACAATTG
>23.31|1615946|33|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
CTGGCGTCCCTGGTGGAATACCTGAAAGGCCTG
>23.32|1616011|33|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
GTGGACCGGGAAGGGAGGGCGTGGGCTGCTAAA
>23.33|1616076|35|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
TCCTTATCGATCCGAACGGATATCATGGCATATAT
>23.34|1616143|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
ATCCGAGAGTTATCACAGCGGGCCGTTTTGCATG
>23.35|1616209|33|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
ATCCTGACAGGCATCAAGGATAAGAAGTTGCAA
>23.36|1616274|34|NZ_LN831776|CRT,PILER-CR
TTCGCCTGGATGAGTGGGACACCTTTCTGTGCGA
>23.37|1616340|32|NZ_LN831776|CRT
TCTTCCCCACGTTGGCTTTGCCAATGTGATTG
>23.38|1616404|33|NZ_LN831776|CRT,CRISPRCasFinder
AGTGCGATTTCCGTATTTACATCGTCCAGGCGA
>23.39|1616469|33|NZ_LN831776|CRT,CRISPRCasFinder
GCTTTACCATTACGAGGGACATTACGGACCTCT
>23.40|1616534|35|NZ_LN831776|CRT,CRISPRCasFinder
TGAAGGATCTCAAAGAAGTATGGGAAAATATACTG
>23.41|1616601|33|NZ_LN831776|CRT,CRISPRCasFinder
CCACGCGTTTGGGAATTTGCTTTCTCAGCCCTC
>23.42|1616666|33|NZ_LN831776|CRT,CRISPRCasFinder
ACCAGCAATAGAACGGTGTTGGCGATACTGATT
>23.43|1616731|36|NZ_LN831776|CRT,CRISPRCasFinder
TGAACAGGGCGACCATTAGCCCGATAGCCATCAATA
>23.44|1616799|35|NZ_LN831776|CRT,CRISPRCasFinder
CCTTCAATGTCAAAAAAGTTCTGTAGGAAGCCAAT
>23.45|1616866|35|NZ_LN831776|CRT,CRISPRCasFinder
AATTCAATAGACGAAGGGCTTTAACCTTGGAGGCC
>23.46|1616933|33|NZ_LN831776|CRT,CRISPRCasFinder
ATTACTCGGGCCTGTGATACGTACCGATCAGTG
>23.47|1616998|34|NZ_LN831776|CRT,CRISPRCasFinder
CTCCAAAGGTGCCTCACGTTCGGCCCAAAATAGA
>23.48|1616340|33|NZ_LN831776|PILER-CR
TTCTTCCCCACGTTGGCTTTGCCAATGTGATTG
>23.49|1616405|33|NZ_LN831776|PILER-CR
AGTGCGATTTCCGTATTTACATCGTCCAGGCGA
>23.50|1616470|33|NZ_LN831776|PILER-CR
GCTTTACCATTACGAGGGACATTACGGACCTCT
>23.51|1616535|35|NZ_LN831776|PILER-CR
TGAAGGATCTCAAAGAAGTATGGGAAAATATACTG
>23.52|1616602|33|NZ_LN831776|PILER-CR
CCACGCGTTTGGGAATTTGCTTTCTCAGCCCTC
>23.53|1616667|33|NZ_LN831776|PILER-CR
ACCAGCAATAGAACGGTGTTGGCGATACTGATT
>23.54|1616732|36|NZ_LN831776|PILER-CR
TGAACAGGGCGACCATTAGCCCGATAGCCATCAATA

CRISPR arrays and Neighbor proteins around NZ_LN831776_23

CRISPR arrays

The CRISPR arrays of NZ_LN831776_23

>merge|NZ_LN831776|23|1613926-1617063|PILER-CR,CRISPRCasFinder,CRT,PILER-CR,CRISPRCasFinder
GTCGCTCCTTATGTGGGAGCGTGGATTGAAATAAACGCTGCACTTAAAGACTTGGCAAAAGTGGAGTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATTCCATATGAAATGTACCGCGCATATGGTGTTTATGGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCCGTTGGCAATCGGCGCAGAAGCAAGGTCATTGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATATCATGACGCGCTGGCACGAGGATGATTTAATCGTCGCTCCTTATGTGGGAGCGTGGATTGAAATAAAGTCCGAGACGTCGAAATCATCGTTCTTGCTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCCGATTGAAGGAAACATCTGGGGAAAAGGATTTATGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATATGATGGATTGTACAAGGATAGCCGCCATGGTGAGTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCACTTATGGTACTACTGAAAAGGCGTTGAGTGGAAGTCGCTCCTTATGTGGGAGCGTGGATTGAAATATTGCCAATGTCCTCTTGAAGCTTCTCATAGCGCGTCGCTCCTTATGTGGGAGCGTGGATTGAAATACATGGCACCGTTTGTCCGGTGCTGTCTATGTGTAGTCGCTCCTTATGTGGGAGCGTGGATTGAAATAGCATCATCCGCCCGTATCTTCTCTGCTTCACGCGTCGCTCCTTATGTGGGAGCGTGGATTGAAATACCCCATCCATTTGTAACTATGGGCTGTGACATGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCTCAGTTAAATGTGGGTACTTTGTGAATAAGTCCTGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCGTCAACTATCACACACTCGCGTCAATCCGTCACGTCGCTCCTTATGTGGGAGCGTGGATTGAAATATTAGTTGAATAACCCCTTGACCTGATGTGCGATAGTCGCTCCTTATGTGGGAGCGTGGATTGAAATAGCAGCAGTCTAATCATATAGATTTAGAGTATCCGTCGCTCCTTATGTGGGAGCGTGGATTGAAATTCAGTTTCCGCAGCCTTTGCATTTTCGGCTTTATGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCACTGCCTAAGACGGAGCGAGCCGCAGCGAAATGTCGCTCCTTATGTGGGAGCGTGGATTGAAATATAAACTCAACCTGTTTGACTCACACAGCTTTGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCAGCACCCGATCAAAATCCAGTCCACCCAGGAGTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATGGAAGTAGAGAGCCTTACGAGCCACAAGACACACTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATGGCACGGGACAAACTGGATGATTTATTGCTGGGTCGCTCCTTATGTGGGAGCGTGGATTGAAATAGGCTTGCCTAATTGTAATAATTTGTCGTAAATAGTCGCTCCTTATGTGGGAGCGTGGATTGAAATAAATTGCTATTAATAATGCAAATATTGCAGCAAGGTCGCTCCTTACGTAGGGGCGTGGATTGAAATCTATCCGTGAAGACCTTTTCCCACGGCCCCCAATGTCGCTCCTTACGTAGGGGCGTGGATTGAAATAGGAGATCCGGATCAGCGCGCAGCTGCTTCGTATCTGTCGCTCCTTACGTAGGGGCGTGGATTGAAATACAATATTGGAATGCAAAACCTGTTTTCACATCCCGTCGCTCCTTACGTAGGGGCGTGGATTGAAATTTGTTTGCAATTTAATTAATGAATACTTATGTATGTCGCTCCTTACGTAGGGGCGTGGATTGAAATTCTCATAACCAGAGATGGTACCATTAGAAACTCCGTCGCTCCTTACGTAGGGGCGTGGATTGAAATTAAAATACAAAAACATTACCGAACCAACAATTGGTCGCTCCTTACGTAGGGGCGTGGATTGAAATCTGGCGTCCCTGGTGGAATACCTGAAAGGCCTGGTCGCTCCTTACGTAGGGGCGTGGATTGAAATGTGGACCGGGAAGGGAGGGCGTGGGCTGCTAAAGTCGCTCCTTACGTAGGGGAGTGGATTGAAATTCCTTATCGATCCGAACGGATATCATGGCATATATGTCGCTTCTTACGTAGGGGCGTGGATTGAAATATCCGAGAGTTATCACAGCGGGCCGTTTTGCATGGTCGCTCCTTACGTAGGGGCGTGGATTGAAATATCCTGACAGGCATCAAGGATAAGAAGTTGCAAGTCGCTCCTTACGTAGGGGCGTGGATTGAAATTTCGCCTGGATGAGTGGGACACCTTTCTGTGCGAGTCGCTCCTTACGAGGGGCGTGGATTGAAATTTCTTCCCCACGTTGGCTTTGCCAATGTGATTGGTCGCTCCTTATGTAGGAGCGTGGATTGAAATAGTGCGATTTCCGTATTTACATCGTCCAGGCGAGTCGCTCCTTATGTAGGAGCGTGGATTGAAATGCTTTACCATTACGAGGGACATTACGGACCTCTGTCGCTCCTTATGTAGGAGCGTGGATTGAAATTGAAGGATCTCAAAGAAGTATGGGAAAATATACTGGTCGCTCCTTACGGAGGAGCGTGGATTGAAATCCACGCGTTTGGGAATTTGCTTTCTCAGCCCTCGTCGCTCCTTACGTAGGAGCGTGGATTGAAATACCAGCAATAGAACGGTGTTGGCGATACTGATTGTCGCTCCTTATGTAGGAGCGTGGATTGAAATTGAACAGGGCGACCATTAGCCCGATAGCCATCAATAGTCGCTCCTTATGTAGGAGCGTGGATTGAAATCCTTCAATGTCAAAAAAGTTCTGTAGGAAGCCAATGTCGCTCCTTATGTAGGAGCGTGGATTGAAATAATTCAATAGACGAAGGGCTTTAACCTTGGAGGCCGTCGCTCCTTATATAGGAGTGTGGATTGAAATATTACTCGGGCCTGTGATACGTACCGATCAGTGGTCGCTCCTTACGGAGGAGCGTGGATTGAAATCTCCAAAGGTGCCTCACGTTCGGCCCAAAATAGAGCCGCTCCTTACATAGGAACGTACATCTAAAT

>NZ_LN831776|23|3|1613926-1615481|PILER-CR
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AAACGCTGCACTTAAAGACTTGGCAAAAGTGGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TCCATATGAAATGTACCGCGCATATGGTGTTTATGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCGTTGGCAATCGGCGCAGAAGCAAGGTCATTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATCATGACGCGCTGGCACGAGGATGATTTAATC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AAAGTCCGAGACGTCGAAATCATCGTTCTTGCT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCGATTGAAGGAAACATCTGGGGAAAAGGATTTATG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATGATGGATTGTACAAGGATAGCCGCCATGGTGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CACTTATGGTACTACTGAAAAGGCGTTGAGTGGAA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATTGCCAATGTCCTCTTGAAGCTTCTCATAGCGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACATGGCACCGTTTGTCCGGTGCTGTCTATGTGTA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGCATCATCCGCCCGTATCTTCTCTGCTTCACGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACCCCATCCATTTGTAACTATGGGCTGTGACATG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CTCAGTTAAATGTGGGTACTTTGTGAATAAGTCCTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGTCAACTATCACACACTCGCGTCAATCCGTCAC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATTAGTTGAATAACCCCTTGACCTGATGTGCGATA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGCAGCAGTCTAATCATATAGATTTAGAGTATCC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TCAGTTTCCGCAGCCTTTGCATTTTCGGCTTTAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CACTGCCTAAGACGGAGCGAGCCGCAGCGAAAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATAAACTCAACCTGTTTGACTCACACAGCTTTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CAGCACCCGATCAAAATCCAGTCCACCCAGGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GGAAGTAGAGAGCCTTACGAGCCACAAGACACACT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GGCACGGGACAAACTGGATGATTTATTGCTGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGGCTTGCCTAATTGTAATAATTTGTCGTAAATA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAATAAATTGCTATTAATAATGCAAATATTGCAGCAAGGTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	CTATCCGTGAAGACCTTTTCCCACGGCCCCCAAT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	AGGAGATCCGGATCAGCGCGCAGCTGCTTCGTATCT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	ACAATATTGGAATGCAAAACCTGTTTTCACATCCC
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TTGTTTGCAATTTAATTAATGAATACTTATGTAT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TCTCATAACCAGAGATGGTACCATTAGAAACTCC
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TAAAATACAAAAACATTACCGAACCAACAATTG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	CTGGCGTCCCTGGTGGAATACCTGAAAGGCCTG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	GTGGACCGGGAAGGGAGGGCGTGGGCTGCTAAA
GTCGCTCCTTACGTAGGGGAGTGGATTGAAAT	TCCTTATCGATCCGAACGGATATCATGGCATATAT
GTCGCTTCTTACGTAGGGGCGTGGATTGAAAT	ATCCGAGAGTTATCACAGCGGGCCGTTTTGCATG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	ATCCTGACAGGCATCAAGGATAAGAAGTTGCAA
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TTCGCCTGGATGAGTGGGACACCTTTCTGTGCGA
GTCGCTCCTTACGAGGGGCGTGGATTGAAATT	TCTTCCCCACGTTGGCTTTGCCAATGTGATTGG
TCGCTCCTTATGTAGGAGCGTGGATTGAAATA	GTGCGATTTCCGTATTTACATCGTCCAGGCGAG
TCGCTCCTTATGTAGGAGCGTGGATTGAAATG	CTTTACCATTACGAGGGACATTACGGACCTCTG
TCGCTCCTTATGTAGGAGCGTGGATTGAAATT	GAAGGATCTCAAAGAAGTATGGGAAAATATACTGG
TCGCTCCTTACGGAGGAGCGTGGATTGAAATC	CACGCGTTTGGGAATTTGCTTTCTCAGCCCTCG
TCGCTCCTTACGTAGGAGCGTGGATTGAAATA	CCAGCAATAGAACGGTGTTGGCGATACTGATTG
TCGCTCCTTATGTAGGAGCGTGGATTGAAATT	GAACAGGGCGACCATTAGCCCGATAGCCATCAATAG


>NZ_LN831776|23|23|1613926-1616274|CRISPRCasFinder
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AAACGCTGCACTTAAAGACTTGGCAAAAGTGGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TCCATATGAAATGTACCGCGCATATGGTGTTTATGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCGTTGGCAATCGGCGCAGAAGCAAGGTCATTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATCATGACGCGCTGGCACGAGGATGATTTAATC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AAAGTCCGAGACGTCGAAATCATCGTTCTTGCT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCGATTGAAGGAAACATCTGGGGAAAAGGATTTATG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATGATGGATTGTACAAGGATAGCCGCCATGGTGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CACTTATGGTACTACTGAAAAGGCGTTGAGTGGAA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATTGCCAATGTCCTCTTGAAGCTTCTCATAGCGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACATGGCACCGTTTGTCCGGTGCTGTCTATGTGTA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGCATCATCCGCCCGTATCTTCTCTGCTTCACGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACCCCATCCATTTGTAACTATGGGCTGTGACATG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CTCAGTTAAATGTGGGTACTTTGTGAATAAGTCCTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGTCAACTATCACACACTCGCGTCAATCCGTCAC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATTAGTTGAATAACCCCTTGACCTGATGTGCGATA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGCAGCAGTCTAATCATATAGATTTAGAGTATCC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TCAGTTTCCGCAGCCTTTGCATTTTCGGCTTTAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CACTGCCTAAGACGGAGCGAGCCGCAGCGAAAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATAAACTCAACCTGTTTGACTCACACAGCTTTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CAGCACCCGATCAAAATCCAGTCCACCCAGGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GGAAGTAGAGAGCCTTACGAGCCACAAGACACACT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GGCACGGGACAAACTGGATGATTTATTGCTGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGGCTTGCCTAATTGTAATAATTTGTCGTAAATA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AAATTGCTATTAATAATGCAAATATTGCAGCAAG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	CTATCCGTGAAGACCTTTTCCCACGGCCCCCAAT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	AGGAGATCCGGATCAGCGCGCAGCTGCTTCGTATCT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	ACAATATTGGAATGCAAAACCTGTTTTCACATCCC
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TTGTTTGCAATTTAATTAATGAATACTTATGTAT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TCTCATAACCAGAGATGGTACCATTAGAAACTCC
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TAAAATACAAAAACATTACCGAACCAACAATTG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	CTGGCGTCCCTGGTGGAATACCTGAAAGGCCTG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	GTGGACCGGGAAGGGAGGGCGTGGGCTGCTAAA
GTCGCTCCTTACGTAGGGGAGTGGATTGAAAT	TCCTTATCGATCCGAACGGATATCATGGCATATAT
GTCGCTTCTTACGTAGGGGCGTGGATTGAAAT	ATCCGAGAGTTATCACAGCGGGCCGTTTTGCATG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	ATCCTGACAGGCATCAAGGATAAGAAGTTGCAA
GTCGCTCCTTACGTAGGGGCGTGGATTGAAATTTCGCCTGGATGAGTGGGACACCTTTCTGTGCGAGTCGCTCCTTACGAGGGGCGTGGATTGAAATTTCTTCCCCACGTTGGCTTTGCCAATGTGATTGGTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	AGTGCGATTTCCGTATTTACATCGTCCAGGCGA
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	GCTTTACCATTACGAGGGACATTACGGACCTCT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	TGAAGGATCTCAAAGAAGTATGGGAAAATATACTG
GTCGCTCCTTACGGAGGAGCGTGGATTGAAAT	CCACGCGTTTGGGAATTTGCTTTCTCAGCCCTC
GTCGCTCCTTACGTAGGAGCGTGGATTGAAAT	ACCAGCAATAGAACGGTGTTGGCGATACTGATT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	TGAACAGGGCGACCATTAGCCCGATAGCCATCAATA
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	CCTTCAATGTCAAAAAAGTTCTGTAGGAAGCCAAT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	AATTCAATAGACGAAGGGCTTTAACCTTGGAGGCC
GTCGCTCCTTATATAGGAGTGTGGATTGAAAT	ATTACTCGGGCCTGTGATACGTACCGATCAGTG
GTCGCTCCTTACGGAGGAGCGTGGATTGAAAT	CTCCAAAGGTGCCTCACGTTCGGCCCAAAATAGA


>NZ_LN831776|23|3|1613926-1617063|CRT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AAACGCTGCACTTAAAGACTTGGCAAAAGTGGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TCCATATGAAATGTACCGCGCATATGGTGTTTATGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCGTTGGCAATCGGCGCAGAAGCAAGGTCATTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATCATGACGCGCTGGCACGAGGATGATTTAATC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AAAGTCCGAGACGTCGAAATCATCGTTCTTGCT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCGATTGAAGGAAACATCTGGGGAAAAGGATTTATG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATGATGGATTGTACAAGGATAGCCGCCATGGTGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CACTTATGGTACTACTGAAAAGGCGTTGAGTGGAA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATTGCCAATGTCCTCTTGAAGCTTCTCATAGCGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACATGGCACCGTTTGTCCGGTGCTGTCTATGTGTA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGCATCATCCGCCCGTATCTTCTCTGCTTCACGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACCCCATCCATTTGTAACTATGGGCTGTGACATG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CTCAGTTAAATGTGGGTACTTTGTGAATAAGTCCTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGTCAACTATCACACACTCGCGTCAATCCGTCAC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATTAGTTGAATAACCCCTTGACCTGATGTGCGATA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGCAGCAGTCTAATCATATAGATTTAGAGTATCC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TCAGTTTCCGCAGCCTTTGCATTTTCGGCTTTAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CACTGCCTAAGACGGAGCGAGCCGCAGCGAAAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATAAACTCAACCTGTTTGACTCACACAGCTTTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CAGCACCCGATCAAAATCCAGTCCACCCAGGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GGAAGTAGAGAGCCTTACGAGCCACAAGACACACT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GGCACGGGACAAACTGGATGATTTATTGCTGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGGCTTGCCTAATTGTAATAATTTGTCGTAAATA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AAATTGCTATTAATAATGCAAATATTGCAGCAAG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	CTATCCGTGAAGACCTTTTCCCACGGCCCCCAAT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	AGGAGATCCGGATCAGCGCGCAGCTGCTTCGTATCT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	ACAATATTGGAATGCAAAACCTGTTTTCACATCCC
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TTGTTTGCAATTTAATTAATGAATACTTATGTAT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TCTCATAACCAGAGATGGTACCATTAGAAACTCC
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TAAAATACAAAAACATTACCGAACCAACAATTG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	CTGGCGTCCCTGGTGGAATACCTGAAAGGCCTG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	GTGGACCGGGAAGGGAGGGCGTGGGCTGCTAAA
GTCGCTCCTTACGTAGGGGAGTGGATTGAAAT	TCCTTATCGATCCGAACGGATATCATGGCATATAT
GTCGCTTCTTACGTAGGGGCGTGGATTGAAAT	ATCCGAGAGTTATCACAGCGGGCCGTTTTGCATG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	ATCCTGACAGGCATCAAGGATAAGAAGTTGCAA
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TTCGCCTGGATGAGTGGGACACCTTTCTGTGCGA
GTCGCTCCTTACGAGGGGCGTGGATTGAAATT	TCTTCCCCACGTTGGCTTTGCCAATGTGATTG
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	AGTGCGATTTCCGTATTTACATCGTCCAGGCGA
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	GCTTTACCATTACGAGGGACATTACGGACCTCT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	TGAAGGATCTCAAAGAAGTATGGGAAAATATACTG
GTCGCTCCTTACGGAGGAGCGTGGATTGAAAT	CCACGCGTTTGGGAATTTGCTTTCTCAGCCCTC
GTCGCTCCTTACGTAGGAGCGTGGATTGAAAT	ACCAGCAATAGAACGGTGTTGGCGATACTGATT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	TGAACAGGGCGACCATTAGCCCGATAGCCATCAATA
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	CCTTCAATGTCAAAAAAGTTCTGTAGGAAGCCAAT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	AATTCAATAGACGAAGGGCTTTAACCTTGGAGGCC
GTCGCTCCTTATATAGGAGTGTGGATTGAAAT	ATTACTCGGGCCTGTGATACGTACCGATCAGTG
GTCGCTCCTTACGGAGGAGCGTGGATTGAAAT	CTCCAAAGGTGCCTCACGTTCGGCCCAAAATAGA
GCCGCTCCTTACATAGGAACGTACATCTAAAT

>NZ_LN831776|23|4|1615516-1616798|PILER-CR
	AAACGCTGCACTTAAAGACTTGGCAAAAGTGGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TCCATATGAAATGTACCGCGCATATGGTGTTTATGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCGTTGGCAATCGGCGCAGAAGCAAGGTCATTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATCATGACGCGCTGGCACGAGGATGATTTAATC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AAAGTCCGAGACGTCGAAATCATCGTTCTTGCT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCGATTGAAGGAAACATCTGGGGAAAAGGATTTATG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATGATGGATTGTACAAGGATAGCCGCCATGGTGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CACTTATGGTACTACTGAAAAGGCGTTGAGTGGAA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATTGCCAATGTCCTCTTGAAGCTTCTCATAGCGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACATGGCACCGTTTGTCCGGTGCTGTCTATGTGTA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGCATCATCCGCCCGTATCTTCTCTGCTTCACGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACCCCATCCATTTGTAACTATGGGCTGTGACATG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CTCAGTTAAATGTGGGTACTTTGTGAATAAGTCCTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGTCAACTATCACACACTCGCGTCAATCCGTCAC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATTAGTTGAATAACCCCTTGACCTGATGTGCGATA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGCAGCAGTCTAATCATATAGATTTAGAGTATCC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TCAGTTTCCGCAGCCTTTGCATTTTCGGCTTTAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CACTGCCTAAGACGGAGCGAGCCGCAGCGAAAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATAAACTCAACCTGTTTGACTCACACAGCTTTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CAGCACCCGATCAAAATCCAGTCCACCCAGGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GGAAGTAGAGAGCCTTACGAGCCACAAGACACACT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GGCACGGGACAAACTGGATGATTTATTGCTGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGGCTTGCCTAATTGTAATAATTTGTCGTAAATA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAATAAATTGCTATTAATAATGCAAATATTGCAGCAAGGTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	CTATCCGTGAAGACCTTTTCCCACGGCCCCCAAT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	AGGAGATCCGGATCAGCGCGCAGCTGCTTCGTATCT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	ACAATATTGGAATGCAAAACCTGTTTTCACATCCC
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TTGTTTGCAATTTAATTAATGAATACTTATGTAT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TCTCATAACCAGAGATGGTACCATTAGAAACTCC
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TAAAATACAAAAACATTACCGAACCAACAATTG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	CTGGCGTCCCTGGTGGAATACCTGAAAGGCCTG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	GTGGACCGGGAAGGGAGGGCGTGGGCTGCTAAA
GTCGCTCCTTACGTAGGGGAGTGGATTGAAAT	TCCTTATCGATCCGAACGGATATCATGGCATATAT
GTCGCTTCTTACGTAGGGGCGTGGATTGAAAT	ATCCGAGAGTTATCACAGCGGGCCGTTTTGCATG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	ATCCTGACAGGCATCAAGGATAAGAAGTTGCAA
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TTCGCCTGGATGAGTGGGACACCTTTCTGTGCGA
GTCGCTCCTTACGAGGGGCGTGGATTGAAATT	TCTTCCCCACGTTGGCTTTGCCAATGTGATTGG
TCGCTCCTTATGTAGGAGCGTGGATTGAAATA	GTGCGATTTCCGTATTTACATCGTCCAGGCGAG
TCGCTCCTTATGTAGGAGCGTGGATTGAAATG	CTTTACCATTACGAGGGACATTACGGACCTCTG
TCGCTCCTTATGTAGGAGCGTGGATTGAAATT	GAAGGATCTCAAAGAAGTATGGGAAAATATACTGG
TCGCTCCTTACGGAGGAGCGTGGATTGAAATC	CACGCGTTTGGGAATTTGCTTTCTCAGCCCTCG
TCGCTCCTTACGTAGGAGCGTGGATTGAAATA	CCAGCAATAGAACGGTGTTGGCGATACTGATTG
TCGCTCCTTATGTAGGAGCGTGGATTGAAATT	GAACAGGGCGACCATTAGCCCGATAGCCATCAATAG
TCGCTCCTTATGTAGGAGCGTGGATTGAAAT

>NZ_LN831776|23|24|1616372-1617063|CRISPRCasFinder
	AAACGCTGCACTTAAAGACTTGGCAAAAGTGGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TCCATATGAAATGTACCGCGCATATGGTGTTTATGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCGTTGGCAATCGGCGCAGAAGCAAGGTCATTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATCATGACGCGCTGGCACGAGGATGATTTAATC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AAAGTCCGAGACGTCGAAATCATCGTTCTTGCT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CCGATTGAAGGAAACATCTGGGGAAAAGGATTTATG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATGATGGATTGTACAAGGATAGCCGCCATGGTGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CACTTATGGTACTACTGAAAAGGCGTTGAGTGGAA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATTGCCAATGTCCTCTTGAAGCTTCTCATAGCGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACATGGCACCGTTTGTCCGGTGCTGTCTATGTGTA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGCATCATCCGCCCGTATCTTCTCTGCTTCACGC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ACCCCATCCATTTGTAACTATGGGCTGTGACATG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CTCAGTTAAATGTGGGTACTTTGTGAATAAGTCCTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGTCAACTATCACACACTCGCGTCAATCCGTCAC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATTAGTTGAATAACCCCTTGACCTGATGTGCGATA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGCAGCAGTCTAATCATATAGATTTAGAGTATCC
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	TCAGTTTCCGCAGCCTTTGCATTTTCGGCTTTAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CACTGCCTAAGACGGAGCGAGCCGCAGCGAAAT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATAAACTCAACCTGTTTGACTCACACAGCTTTG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CAGCACCCGATCAAAATCCAGTCCACCCAGGAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GGAAGTAGAGAGCCTTACGAGCCACAAGACACACT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	GGCACGGGACAAACTGGATGATTTATTGCTGG
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AGGCTTGCCTAATTGTAATAATTTGTCGTAAATA
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	AAATTGCTATTAATAATGCAAATATTGCAGCAAG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	CTATCCGTGAAGACCTTTTCCCACGGCCCCCAAT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	AGGAGATCCGGATCAGCGCGCAGCTGCTTCGTATCT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	ACAATATTGGAATGCAAAACCTGTTTTCACATCCC
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TTGTTTGCAATTTAATTAATGAATACTTATGTAT
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TCTCATAACCAGAGATGGTACCATTAGAAACTCC
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	TAAAATACAAAAACATTACCGAACCAACAATTG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	CTGGCGTCCCTGGTGGAATACCTGAAAGGCCTG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	GTGGACCGGGAAGGGAGGGCGTGGGCTGCTAAA
GTCGCTCCTTACGTAGGGGAGTGGATTGAAAT	TCCTTATCGATCCGAACGGATATCATGGCATATAT
GTCGCTTCTTACGTAGGGGCGTGGATTGAAAT	ATCCGAGAGTTATCACAGCGGGCCGTTTTGCATG
GTCGCTCCTTACGTAGGGGCGTGGATTGAAAT	ATCCTGACAGGCATCAAGGATAAGAAGTTGCAA
GTCGCTCCTTACGTAGGGGCGTGGATTGAAATTTCGCCTGGATGAGTGGGACACCTTTCTGTGCGAGTCGCTCCTTACGAGGGGCGTGGATTGAAATTTCTTCCCCACGTTGGCTTTGCCAATGTGATTGGTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	AGTGCGATTTCCGTATTTACATCGTCCAGGCGA
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	GCTTTACCATTACGAGGGACATTACGGACCTCT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	TGAAGGATCTCAAAGAAGTATGGGAAAATATACTG
GTCGCTCCTTACGGAGGAGCGTGGATTGAAAT	CCACGCGTTTGGGAATTTGCTTTCTCAGCCCTC
GTCGCTCCTTACGTAGGAGCGTGGATTGAAAT	ACCAGCAATAGAACGGTGTTGGCGATACTGATT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	TGAACAGGGCGACCATTAGCCCGATAGCCATCAATA
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	CCTTCAATGTCAAAAAAGTTCTGTAGGAAGCCAAT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	AATTCAATAGACGAAGGGCTTTAACCTTGGAGGCC
GTCGCTCCTTATATAGGAGTGTGGATTGAAAT	ATTACTCGGGCCTGTGATACGTACCGATCAGTG
GTCGCTCCTTACGGAGGAGCGTGGATTGAAAT	CTCCAAAGGTGCCTCACGTTCGGCCCAAAATAGA
GCCGCTCCTTACATAGGAACGTACATCTAAAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020426227.1|1624132_1624627_+|DinB-family-protein	unknown	unknown	gnl|CDD|378981
NZ_LN831776.1|WP_052741421.1|1601927_1602917_+|hypothetical-protein	PD-DExK	mkCas0090_PD-DExK_CAS-I:CAS-III	unknown
NZ_LN831776.1|WP_020431504.1|1610922_1611783_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	COG3649_cas7_CAS-I-C	gnl|CDD|187820
NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	gnl|CDD|273847
NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	gnl|CDD|187887
NZ_LN831776.1|WP_020426224.1|1625250_1625610_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_167330838.1|1624773_1624944_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	gnl|CDD|224124
NZ_LN831776.1|WP_020426223.1|1625730_1626216_+|SprT-family-protein	unknown	unknown	gnl|CDD|235290
NZ_LN831776.1|WP_046501636.1|1623299_1623869_-|CGNR-zinc-finger-domain-containing-protein	unknown	unknown	gnl|CDD|378696
NZ_LN831776.1|WP_020431498.1|1613466_1613757_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl|CDD|187856
NZ_LN831776.1|WP_020431500.1|1612425_1613457_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	gnl|CDD|188360
NZ_LN831776.1|WP_020431436.1|1601115_1601931_+|type-III-B-CRISPR-module-RAMP-protein-Cmr6	cmr6gr7	COG1604_cmr6gr7_CAS-III-B	gnl|CDD|224520
NZ_LN831776.1|WP_020431502.1|1611772_1612429_+|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl|CDD|224385
NZ_LN831776.1|WP_046501630.1|1617329_1618190_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|197666
NZ_LN831776.1|WP_020431435.1|1600719_1601094_+|type-III-B-CRISPR-module-associated-protein-Cmr5	cmr5gr11	COG3337_cmr5gr11_CAS-III-B	gnl|CDD|378242
NZ_LN831776.1|WP_020426222.1|1626224_1626878_-|pentapeptide-repeat-containing-protein	unknown	unknown	gnl|CDD|224276
NZ_LN831776.1|WP_020426225.1|1625027_1625165_-|cortex-morphogenetic-protein-CmpA	unknown	unknown	gnl|CDD|380221
NZ_LN831776.1|WP_020426229.1|1622135_1623242_+|GGDEF-domain-containing-protein	unknown	unknown	gnl|CDD|143635
NZ_LN831776.1|WP_046501633.1|1618215_1619322_-|linear-amide-C-N-hydrolase	unknown	unknown	gnl|CDD|367486

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831776.1|WP_020431498.1|1613466_1613757_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	1.1e-31	103.6	1.1
NZ_LN831776.1|WP_020431500.1|1612425_1613457_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	3.4e-146	481.3	0.2
NZ_LN831776.1|WP_020431436.1|1601115_1601931_+|type-III-B-CRISPR-module-RAMP-protein-Cmr6	cmr6gr7	COG1604_cmr6gr7_CAS-III-B	1.3e-50	167.1	0.0
NZ_LN831776.1|WP_052741421.1|1601927_1602917_+|hypothetical-protein	PD-DExK	mkCas0090_PD-DExK_CAS-I:CAS-III	8.9e-27	87.9	0.3
NZ_LN831776.1|WP_020431504.1|1610922_1611783_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	COG3649_cas7_CAS-I-C	2.3e-127	418.8	0.8
NZ_LN831776.1|WP_020431502.1|1611772_1612429_+|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	9.6e-35	114.8	1.6
NZ_LN831776.1|WP_020431435.1|1600719_1601094_+|type-III-B-CRISPR-module-associated-protein-Cmr5	cmr5gr11	COG3337_cmr5gr11_CAS-III-B	4.9e-21	69.9	0.0
NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	7.7e-161	531.0	1.6
NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	3.3e-85	281.5	7.6
NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	1e-60	199.7	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020426227.1|1624132_1624627_+|DinB-family-protein	gnl|CDD|378981	pfam12867, DinB_2, DinB superfamily. The DinB family are an uncharacterized family of potential enzymes. The structure of these proteins is composed of a four helix bundle.	3.53876e-08
NZ_LN831776.1|WP_020431435.1|1600719_1601094_+|type-III-B-CRISPR-module-associated-protein-Cmr5	gnl|CDD|378242	pfam09701, Cas_Cmr5, CRISPR-associated protein (Cas_Cmr5). CRISPR is a term for Clustered, Regularly Interspaced Short Palindromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This family, represented by TM1791.1 of Thermotoga maritima, is found in both archaeal and bacterial species.	2.24088e-19
NZ_LN831776.1|WP_046501633.1|1618215_1619322_-|linear-amide-C-N-hydrolase	gnl|CDD|367486	pfam03417, AAT, Acyl-coenzyme A:6-aminopenicillanic acid acyl-transferase.	1.24319e-30
NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5	gnl|CDD|273847	TIGR01876, cas_Cas5d, CRISPR-associated protein Cas5, subtype I-C/DVULG. CRISPR is a term for Clustered, Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This small Cas family is represented by CT1134 of Chlorobium tepidum. This family belongs to a set of several Cas protein families, one each for a number of different CRISPR/Cas subtypes, that share a region of N-terminal sequence similarity modeled by TIGR02593. This family represents the Dvulg subtype of CRISPR/Cas locus.	3.09357e-90
NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	gnl|CDD|187887	cd09757, Cas8c_I-C, CRISPR/Cas system-associated protein Cas8c. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Zn-finger domain containing protein, distant homologs of Cas8 proteins; signature gene for I-C subtype; also known as Csd1 family.	2.89947e-169
NZ_LN831776.1|WP_020426222.1|1626224_1626878_-|pentapeptide-repeat-containing-protein	gnl|CDD|224276	COG1357, COG1357, Pentapeptide repeats containing protein [Function unknown].	2.22208e-16
NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3	gnl|CDD|224124	COG1203, COG1203, CRISPR-associated helicase Cas3 [Defense mechanisms].	7.24875e-69
NZ_LN831776.1|WP_020426223.1|1625730_1626216_+|SprT-family-protein	gnl|CDD|235290	PRK04351, PRK04351, SprT family protein.	4.70474e-78
NZ_LN831776.1|WP_046501636.1|1623299_1623869_-|CGNR-zinc-finger-domain-containing-protein	gnl|CDD|378696	pfam11706, zf-CGNR, CGNR zinc finger. This family consists of a C-terminal zinc finger domain. It seems likely to be DNA-binding given the conservation of many positively charged residues. The domain is named after a highly conserved motif found in many members of the family.	1.66574e-19
NZ_LN831776.1|WP_020431498.1|1613466_1613757_+|CRISPR-associated-endonuclease-Cas2	gnl|CDD|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	1.93294e-34
NZ_LN831776.1|WP_020431500.1|1612425_1613457_+|type-I-C-CRISPR-associated-endonuclease-Cas1	gnl|CDD|188360	TIGR03640, cas1_DVULG, CRISPR-associated endonuclease Cas1, subtype I-C/DVULG. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes the Cas1 protein particular to the DVULG subtype of CRISPR/Cas system.	0
NZ_LN831776.1|WP_020431436.1|1601115_1601931_+|type-III-B-CRISPR-module-RAMP-protein-Cmr6	gnl|CDD|224520	COG1604, COG1604, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	6.42086e-57
NZ_LN831776.1|WP_020431502.1|1611772_1612429_+|CRISPR-associated-protein-Cas4	gnl|CDD|224385	COG1468, COG1468, CRISPR-associated protein Cas4 (RecB family exonuclease) [Defense mechanisms].	1.41191e-27
NZ_LN831776.1|WP_046501630.1|1617329_1618190_-|helix-turn-helix-domain-containing-protein	gnl|CDD|197666	smart00342, HTH_ARAC, helix_turn_helix, arabinose operon control protein.	5.79213e-25
NZ_LN831776.1|WP_020426225.1|1625027_1625165_-|cortex-morphogenetic-protein-CmpA	gnl|CDD|380221	NF033225, spore_CmpA, cortex morphogenetic protein CmpA. Members of this family are CmpA (cortex morphogenetic protein A), a small protein (37 amino acids) involved in endospore formation and frequently missed during genome annotation.	1.76744e-17
NZ_LN831776.1|WP_020426229.1|1622135_1623242_+|GGDEF-domain-containing-protein	gnl|CDD|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	2.76115e-51
NZ_LN831776.1|WP_020431504.1|1610922_1611783_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	gnl|CDD|187820	cd09689, Cas7_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas7. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas7 is a RAMP superfamily protein; Subunit of the Cascade complex; also known as Csd2 family.	9.02891e-134

Protein sequences

>NZ_LN831776.1|WP_020431498.1|1613466_1613757_+|CRISPR-associated-endonuclease-Cas2
MLVVITYDVSTLSGEGQSRLRKVSKICQNYGQRVQNSVFECVVDAAQFAELKIKLKTIIDDDEDSIRFYQLGNNHKNKVEHVGIKKSIDLEGPLIL
>NZ_LN831776.1|WP_020431500.1|1612425_1613457_+|type-I-C-CRISPR-associated-endonuclease-Cas1
MKKLLNTLYITQPSVYLSLDGDNVVLLKEEEKLGRFPLHNLESIVTFGYTGASPALMGYCADSNISLLFLTMNGRYLARVTGQSRGNVVLRKKQYNLSEDEVRSAKIARNFIIGKIYNHKWMLERMTRDYPLRVNVELFKETSQQLSSLILEVRACEQLDRLRGLEGQAAATYYSQFNQMILQQKEDFYFHSRTRRPPLDNVNAMLSLAYTLLTHDTASALEAVGLDAYVGFLHRDRPGRVSLALDVMEELRGVFADKFVLTLINKKLISKADFLKKENGAVIMTDEARKKFLAAWQSKKQETITHPYLGEKISWGLVPHAQALLLARHLRNDLDEYPPFLWK
>NZ_LN831776.1|WP_020431502.1|1611772_1612429_+|CRISPR-associated-protein-Cas4
MEYDDEDELMLSGIQHFHFCKRQWALIHIEQQWEENVRTIEGQHLHRNADQPLIREKRVDKIIVRAMPVKSRELNISGICDVVEFIRDDSGVEINGADGKYAAYPVEYKRGKPKREDEDILQLAAQAMCLEEMLLCEVSTGYIFYNEIKHRIEVPLTAELKANVKAIVEVMQSYYHRRHTPKVKTGPFCKSCSLQHICLPKLMNKQSVKSYVEGKIRE
>NZ_LN831776.1|WP_020431504.1|1610922_1611783_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2
MTILDHKIDFAVIVSVTKANPNGDPLNGNRPRQNYDGYGEISDVALKRKIRNRLQDMGESIFVQSNDRKSDSYNSLRERADANAELDKILKAKGSSNEEFARIACQEWLDVRSFGQVFAFKADKGAGVSVGVRGPVSIHTATSVSPIDITSMQITKSVNSEPGKDRGSDTMGMKHRVDFGVYVFYGSINTQLAEKTGFSNEDAEKIKQVLVTLFENDASAARPDGSMEVHKVYWWEHNSKLGQYSSAKVHRSLVVRPKVDDPKTIADYEIVVSEMEGLKAEVIDGI
>NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1
MSWLLNLYETYQSNQDCVGVIETRYNDREYTLLPVSHTTQNAHIEVNVTEDGEFHSASVLDKSESSTLIPCTEDSASRAGSKVAPYPLHDKLSYVAGDFLAYGGKIKKEEPFAAYIKQLGGWADSPYACPKVKSIHSYLSKRRLIQDLVSHSILFLDADHQLIEKWDKKYEALHGEKPLIFSAVAGEQESAFIRFNVYSPDKELTKVWKDPEMYDSFMQYYSHLLGQEDYCYVTGRMLPSTDRHANKIRNAADKAKLISSNDTSGFTFRGRFTQSSDAASISYEVSQKAHNALKWLINRQGKIVDQRVFLVWGNDDLNIPDPTEDFFSFDLEPAVARERKSYTHKEYAGEIAKAMDGYRNKLASEYKSDVNILVLDSATTGRLAVLYYRNMDKQLYLDKLVHWHSTCSWLHRYRKNTQDEWVEFYGASATKDIAFAAYGPKANEKIVKGVMERLLPCIVDGHNIPQDIVRSAFYRASNPVSMEKWEWEKTLSITCALINAKEEMNVALDTEIDDRSYLFGRLLAIADVLERRALDSDEKRSTNAIRYMNAFSQHPERTWNTIQQSIQPHQARLGTKLRYYSSLIDEVASKIPLDQFNNKPLSGKYLLGFYSQRHELYQKKDKNNDSIQASENGER
>NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5
MRNSIEFKVYGKYALFTDPLTKLGGEKLTYSVPTYQALKGIVESIYWKPTIHIIVEEVRIMNAIRMESKGIRPMDYGGGNTLANYTYLKDVCYEVRAHFEFNMNRPDLEHDRNEHKHHNLLKRSLQAGGRRDIFLGARECQAYVEPCVFGVERGFYNDYGDIHLGSMVHGINYPDETGRDEMEVRLWSPVMRDGIIRFIRPEECTQVRRIAEMKPKSFNETNLQTAEELLAQIEAEEKA
>NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3
MEYIAHIRESDMKVQTVTEHLLEVRTLAEKYGKKLGIKYMAGLAGMLHDLGKYTEEFRNYIVQAVYHPEAPPSRGSVDHSTAGGKLLFERFHRVPADLSNKEAHINKMILAEVVGNAILSHHSYLQDFLNPDSESNFLNRVQDKCLPEFERAKDSFFELVMNETEFHLYVDKAVEELSDYLKVDSSSTTELKLMFLTKYVFSALIDADRTNTRCFEENQPDPSYNPQQLFSAYYTKLMTKIDSFHNHKHAHSAINQLRQGMSEQCEQFAAEPSGIYTLSIPTGGGKTLASLRYALKHALLKEKKHIIYVVPYTTIIEQNANEIRSILKDDEHILEHHSNVVEEETQDDEHEDGSLSLRQKLKLAKDNWDAPIIFTTMVQFLNVFYADGSRNIRRLHNLSESVIVFDEVQKVPVRCVSLFNQALNFLKSYAHSSIVLCTATQPELDYVRLKLEIEPEAEMIHNLDHVIEAFRRVEIVDRATNEHFDNDTLTEFVITQMREVSSVLVILNTKSVVQALYRSLNERNLSVPIYHLSTSMCAAHRNQILDKVKALLEDKEPVICISTQLIEAGVDVSFQCVIRSLAGLDSIAQAAGRCNRHGEDLIRQVYVIDHIEENLKHLKEIKIGKEISRKILIDLSRDASLHGGHILSIQAMEKYFKEFYTELATSLNYSIPKLGQEMTTLLSGPRKNNAYYQAYLSKHRAALPLFLLNSYKTAAENFQVIDNLTTTVVVPFGDGPEEGKDIIAELNGQQSIPDLTRLLRKAQQYTINIYSYEKDLLSKNGSLVPYLDGKILALKEGAYHPEYGLNLENDSPLDMYMF
>NZ_LN831776.1|WP_052741421.1|1601927_1602917_+|hypothetical-protein
MKDKQPSSEQELEEMRKAAPKIIQQIAQNYIHLEESITSQLRMAAGSHHVTSGTFREDIWKSLFEQIIPRKFSIEQSVFIIDSHGLVSKEVDLAIFDEQYTPYIFRLGRIKYIPIEAVAVVVQCKSNNIHGRNKRENLRTWSKSITNLKTSLKSVARIHTGIAKGEYDYILDKDGQLRIEPEKLEKSDRDKLAQTSTRPIQILCHTKDTSSSKYDDLFDIVIHPEGERLRVEMKPDLKDLPSWYDSLNHKQDPRYEHIVKPFDTKEPSEDFQKALQVDNYKVYKDKARTKEIGLLSLTFQLNQLLMLINNPILFPHMAYVDMFNTNISK
>NZ_LN831776.1|WP_020431436.1|1601115_1601931_+|type-III-B-CRISPR-module-RAMP-protein-Cmr6
MNAYLAITKQEASNKGSKLYRVVNGDLQNTKGEFYRQLIKEYQADWKQSCIWYEQRYEHYSTKLHDTLGDSRCIEFEMASISPLLIGHGGVSALETSLMLHRIYGVPYIPGSAIKGVTANYCHCMLGAENPAFLSDGEYYEALFGSQDQAGYINYEDAWVTPATAESALIDDVMTPHHQNYNSIQLQRTDQQKASAPRDDDDPVPLPFLAVNASFRFLLTCPSDRVEKEDARQWLNIAQEIVSHALQYEGIGGKTNAGYGRMLQADRRERE
>NZ_LN831776.1|WP_020431435.1|1600719_1601094_+|type-III-B-CRISPR-module-associated-protein-Cmr5
MKSAAHTYAEKAMQSIRSVEADPDCNNKDYGRLCLLFPSMVQVNGLRLTVAFFQSKGKSQKTLHQRYLQDLAAAVGSAAWETGLSTNDMMDYRDLTRHVLQAAVWFKRYAEAILKVEAADGLDS
>NZ_LN831776.1|WP_046501630.1|1617329_1618190_-|helix-turn-helix-domain-containing-protein
MINNRAIGEAIVFIENSLYEPIAACDVAKAVSYSYYHFHRYFQAIMGETIGSYIRTRRLTQAAWDLVHSEKKILDIGVSLYFETAESFTRAFKDRYGMTPTEYRKNGIDVLIGNRPPAQISDNIVHPYADLSPQIVTVPETYTMGIRFITTISRNESIAMWQLFNQQIPDTFAGTRYGIFEAGETCAADVFNPQSETTAFVGIEFPKEQPILRGMERKTIRGGKYARFIHKGIVKDLMQTYHYIWGVWFPKSGYELDNRDDFECYTERFAGENIESSEIDIYFPIK
>NZ_LN831776.1|WP_046501633.1|1618215_1619322_-|linear-amide-C-N-hydrolase
MEKTKVYFKNFIGTSYEVGTEIGQWVLSTPSLLKQVLLPPNAYPNDKFTKITDLLDRYCQGINEEIKGFADTIGVSSEQALFYTMTYLERGCSLMAVLPSKSKSGHTLMARNYDFNNEMEEMCFAFTNIKGKYRYIGSTLNLFGRCDGMNEHGLAVCKASNGVPVGNFEGGQKAGATGFSFWVVVRSILENCKTVQEAIEWTMSAPIGYNMNLMLADSSNKIALLQCMDGHKSYKLLDEYSEEAFLSVTNHAVLEDIKPYQKMIIENSVVRNNKIVEVFTGKKQLSKKDMKTLLSTSYPDGLCCHYYKEFFGTLRSMIFDVNDKTIEMTFGSPQVNEWQTFSVGALEMQEVEVLLPQEKARPDFYKIS
>NZ_LN831776.1|WP_020426229.1|1622135_1623242_+|GGDEF-domain-containing-protein
MSPSGTSAYRQAKWIKRFLQTYWLVIALHFLAQLAAYTFLPYERGAHEFYYGVLLYPTLLMGAVVGIAQWIDRRASKYSFISLFMAGTIIAMIIIHLNMDIRIIGALMLLPIFASAIFYRLDLTFFTFALQAVAFFVMYRWDYWFKYFFSSFDLIAIPIFLVVGTLVASIMIINGRELVSDLEASLMAKQDLLIENAVMRKLSTTDALTDLYNHISFHEFYDKALEYGDQGAPFHLALIDIDNFKLINDKYGHRAGDIILARVAKVIRDLISSADIAARYGGEEFAILFFEKTFEEAEAIADKIRLRLSGTPHEEMDGAAVTVSIGLKSYSQGTTKEQLFEEVDALLYAAKHEGKNKVRTPYSSTVFT
>NZ_LN831776.1|WP_046501636.1|1623299_1623869_-|CGNR-zinc-finger-domain-containing-protein
MLWDDFINSYWRDWRTGDRSKDKDKLQDQEWLAVWLEQHSLRAELPPEPKELEQLQQLRSLLREAVQKLVQDCPPDGDLLERLNGYMLMGPVIRQVVQSVEGKVKISFQPQRPDWEQVMAEIASSFAAALVEKDTSRFRICENPDCLWVYYDDTRNRSKRYCDDKMCGNLMKVRRFRARKKAGMEGNSE
>NZ_LN831776.1|WP_020426227.1|1624132_1624627_+|DinB-family-protein
MQNKISDVLLQNWDYVMDIEDWAPPLSAALEGVTSEQAVWKPQGEAGNSIWETVNHLTYYKERLLIKLKGLPKLPEAESNDATFTVTESGEEAWGHAVAKLKQVHASLREVIEALEEGAYDWGGSGHAPGEEVMSLILHDSYHTGQIVLVRKLQGSWPTNRSFN
>NZ_LN831776.1|WP_167330838.1|1624773_1624944_+|hypothetical-protein
MMEPNYKDRSVEVERTEVQKKSDSSVVASTFIKYAAYLIIFFGLLFFLVKYVFPLF
>NZ_LN831776.1|WP_020426225.1|1625027_1625165_-|cortex-morphogenetic-protein-CmpA
MPQWLCHQLMKAYYKKDRRQIKLLNECWFFYRNSAEARDSIQREV
>NZ_LN831776.1|WP_020426224.1|1625250_1625610_-|hypothetical-protein
MPKMRYVILQQHQELQFVEMPEEYAYQLSALNLRLNKEIDKLTADNVPDLPLAIAECDSLELLREEHSLESGLAYINRLESAFSSIQESNYPLISLLTEIRALQAQLEQWYEEEEEGVH
>NZ_LN831776.1|WP_020426223.1|1625730_1626216_+|SprT-family-protein
MSNEELQQWIEQVSQDSFGVPFRHKASFNSRLSTTGGRYFIKSHNIEINPMQLEMFGREETERIIKHELCHYHLHLSKRGYMHRDADFKKLLAMVGGSRFCQTLPGAKARKPLPYRYKLVCTACATEYPRKRKADPKRYRCGNCAGKLKLVALEESRGKAK
>NZ_LN831776.1|WP_020426222.1|1626224_1626878_-|pentapeptide-repeat-containing-protein
MSNKIDPPKITEENALLPQQIHTLQSKEEISHCLISDSLIEYQEADRVSFDKVIFRNVTVTESTLHAIELTDVIFENCDLSNVNFSDAFVHRTEFRNCKLIGTDFSRGRFQNVRIVDCIGDFASFRFGKFKGTVFTNCRLVSSDYYQAELTHIGFSECDIDQATFAGCRLKEIDLSDCSFTGLHVDIEDLAGCIISAEQAASFAGLLGLVIKTDTEL

Crispr_ID: NZ_LN831776_24

• CRISPR_ID: NZ_LN831776_24
• CRISPR_location: 1619873-1622026
• CRISPR_type: TypeI
• Repeat_type: NA:I-C
• Spacer_info: 32 spacers
• Cas_protein_info: cas2,cas1,cas4,cas7,cas8c,cas5,cas3,PD-DExK

Consensus repeat of NZ_LN831776_24

Consensus_repeat	Method
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CRISPRCasFinder
GTCGCTCCTTATNNAGGAGCGTGGATTGAAAT	CRT
AGTCGCTCCTTATACAGGAGCGTGGATTGAAATATATTC	PILER-CR
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	PILER-CR
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	PILER-CR
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CRISPRCasFinder

spacers of NZ_LN831776_24

>24.1|1619905|33|NZ_LN831776|CRISPRCasFinder,CRT
CATTCGAAAATTTTTTTGAAGCGGAGTGTCTTT
>24.2|1619970|35|NZ_LN831776|CRISPRCasFinder,CRT
ATCACGTTTGCGACCGTTAGCTGCGTGTGCTGATC
>24.3|1620037|34|NZ_LN831776|CRISPRCasFinder,CRT
ATTTTCCCGGCATCCATAGCAAACCTCCTGAATA
>24.4|1620103|34|NZ_LN831776|CRISPRCasFinder,CRT
TTACTGTGAATAAACGGTATGTCAACCCTATGGA
>24.5|1620169|35|NZ_LN831776|CRISPRCasFinder,CRT
ATATTCAGATTGTTCCTTCGCAAATTTCTCCCGCT
>24.6|1620236|34|NZ_LN831776|CRISPRCasFinder,CRT
ATCGTCAGCAGCATCCACAATCGTAGATGGTCTT
>24.7|1620302|36|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
TCCACGTTGCCCCATCCGTGATACGGAGACTTACCG
>24.8|1620370|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
TAACGCCGGGTGCAGCAACACGCTGCGGGTACAT
>24.9|1620436|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
GCCGTTTATGCTGATATACGTGTCGATTGCTTAC
>24.10|1620502|35|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
ACATTCTTCCCGGGATGCAGCAGCGTGCCGGTGTG
>24.11|1620569|33|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
TACATCTCTTTCTTGGTCAGGCCCGAAAACAAT
>24.12|1620634|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
CAGAGGATATAATCGATCTGCACTAGACGGTCGT
>24.13|1620700|33|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
CCTCCTACGTATGCTGGGGGGCTAATCTGTACA
>24.14|1620765|35|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
CCCTGGAGGATGTGAACAAGTTTTTGGACATTCGC
>24.15|1620832|35|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
GCGATTACATAATACTGCCGTACTTAGAGGAGATG
>24.16|1620899|35|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
TTATCCCTCCCGTGTATGCTCGCCGGTATTTAAGC
>24.17|1620966|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
ACAGTATGCAGTGATAGAAAGTAGCCCAACCGCC
>24.18|1621032|35|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
TGATAAAAGTCACATTCAAAGCCAGCTGCCTTCAG
>24.19|1621099|36|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
CATGACAAGGATGGACTTGCCGCGTCCGGATCGCGC
>24.20|1621167|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
AGTGATATTACCATACTCATCGCGGGCACGTAAA
>24.21|1621233|35|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
GCTCGATTAACGCCATCTGCGCCGTAATCCGTAGC
>24.22|1621300|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR
AAAACTCGGGTTTAGTGCAGACCAGATGTTTGAT
>24.23|1621366|35|NZ_LN831776|CRISPRCasFinder,CRT
AATACAAACAACATCATTGAGAAAAGGTTAATTCC
>24.24|1621433|35|NZ_LN831776|CRISPRCasFinder,CRT
AAGCTGATCGTCAGTAGCCTCCTGCACAGCACTGA
>24.25|1621500|36|NZ_LN831776|CRISPRCasFinder,CRT
CCCTTAACTAGAGACGTTATGCGCACAGAGATCAGT
>24.26|1621568|34|NZ_LN831776|CRT
CGCTGGCGATTTTAGCGGCCTCCAGATCAATCTT
>24.27|1621634|32|NZ_LN831776|CRT
CAAGGACCGGGAAGGAAAAGCCGTCGCGGAAG
>24.28|1621698|35|NZ_LN831776|CRT,PILER-CR,CRISPRCasFinder
CCTGTGTCGTCCTTTGCTAGTGCGGAAGATTGGAC
>24.29|1621765|32|NZ_LN831776|CRT,PILER-CR,CRISPRCasFinder
ATTGCAACGATCTCTACGATGCTCGGTCCGTA
>24.30|1621829|33|NZ_LN831776|CRT,PILER-CR,CRISPRCasFinder
AAGGACAAACTGTTTGAACGCGATTTGCGAGAT
>24.31|1621894|35|NZ_LN831776|CRT,PILER-CR,CRISPRCasFinder
GGATATCTTTAGAGAAGCAGCGAGGTCTCGATTAT
>24.32|1621961|34|NZ_LN831776|CRT,PILER-CR,CRISPRCasFinder
TTTAATGACTCACGACTAAATGAAATGTGGGCTT
>24.33|1620044|27|NZ_LN831776|PILER-CR
CCGGCATCCATAGCAAACCTCCTGAAT
>24.34|1620110|33|NZ_LN831776|PILER-CR
TTACTGTGAATAAACGGTATGTCAACCCTATGG

CRISPR arrays and Neighbor proteins around NZ_LN831776_24

CRISPR arrays

The CRISPR arrays of NZ_LN831776_24

>merge|NZ_LN831776|24|1619873-1622026|CRISPRCasFinder,CRT,PILER-CR,PILER-CR,PILER-CR,CRISPRCasFinder
GTCGCTCCTTATGTGGGAGCGTGGATTGAAATCATTCGAAAATTTTTTTGAAGCGGAGTGTCTTTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATATCACGTTTGCGACCGTTAGCTGCGTGTGCTGATCGTCGCTCCTTATACAGGAGCGTGGATTGAAATATTTTCCCGGCATCCATAGCAAACCTCCTGAATAGTCGCTCCTTATACAGGAGCGTGGATTGAAATTTACTGTGAATAAACGGTATGTCAACCCTATGGAGTCGCTCCTTATACAGGAGCGTGGATTGAAATATATTCAGATTGTTCCTTCGCAAATTTCTCCCGCTGTCGCTCCTTATACAGGAGCGTGGATTGAAATATCGTCAGCAGCATCCACAATCGTAGATGGTCTTGTCGCTCCTTATACAGGAGCGTGGATTGAAATTCCACGTTGCCCCATCCGTGATACGGAGACTTACCGGTCGCTCCTTATACAGGAGCGTGGATTGAAATTAACGCCGGGTGCAGCAACACGCTGCGGGTACATGTCGCTCCTTATACAGGAGCGTGGATTGAAATGCCGTTTATGCTGATATACGTGTCGATTGCTTACGTCGCTCCTTATACAGGAGCGTGGATTGAAATACATTCTTCCCGGGATGCAGCAGCGTGCCGGTGTGGTCGCTCCTTATACAGGAGCGTGGATTGAAATTACATCTCTTTCTTGGTCAGGCCCGAAAACAATGTCGCTCCTTATACAGGAGCGTGGATTGAAATCAGAGGATATAATCGATCTGCACTAGACGGTCGTGTCGCTCCTTATACAGGAGCGTGGATTGAAATCCTCCTACGTATGCTGGGGGGCTAATCTGTACAGTCGCTCCTTATACAGGAGCGTGGATTGAAATCCCTGGAGGATGTGAACAAGTTTTTGGACATTCGCGTCGCTCCTTATACAGGAGCGTGGATTGAAATGCGATTACATAATACTGCCGTACTTAGAGGAGATGGTCGCTCCTTATACAGGAGCGTGGATTGAAATTTATCCCTCCCGTGTATGCTCGCCGGTATTTAAGCGTCGCTCCTTATACAGGAGCGTGGATTGAAATACAGTATGCAGTGATAGAAAGTAGCCCAACCGCCGTCGCTCCTTATACAGGAGCGTGGATTGAAATTGATAAAAGTCACATTCAAAGCCAGCTGCCTTCAGGTCGCTCCTTATACAGGAGCGTGGATTGAAATCATGACAAGGATGGACTTGCCGCGTCCGGATCGCGCGTCGCTCCTTATACAGGAGCGTGGATTGAAATAGTGATATTACCATACTCATCGCGGGCACGTAAAGTCGCTCCTTATACAGGAGCGTGGATTGAAATGCTCGATTAACGCCATCTGCGCCGTAATCCGTAGCGTTGCTCCTTATACAGGAGCGTGGATTGAAATAAAACTCGGGTTTAGTGCAGACCAGATGTTTGATGTCGCTTCTTATGTAGGAGCGTGGATTGAAATAATACAAACAACATCATTGAGAAAAGGTTAATTCCGTCGCTCCTTATGCAGGAGCGTGGATTGAAATAAGCTGATCGTCAGTAGCCTCCTGCACAGCACTGAGTCGCTCCTTATGTGGGGGCGTGGATCGAAATCCCTTAACTAGAGACGTTATGCGCACAGAGATCAGTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCGCTGGCGATTTTAGCGGCCTCCAGATCAATCTTGTCGCTCCTTATGTAGAGCGTGGATTAAATGGCAAGGACCGGGAAGGAAAAGCCGTCGCGGAAGGTCGCTCCTTATGTAGGAGCGTGGATTGAAATCCTGTGTCGTCCTTTGCTAGTGCGGAAGATTGGACGTCGCTCCTTATGTAGGAGCGTGGATTGAAATATTGCAACGATCTCTACGATGCTCGGTCCGTAGTCGCTCCTTATGCAGGAGCGTGGATTGAAATAAGGACAAACTGTTTGAACGCGATTTGCGAGATGTCGCTCTTTATGTAGGAGCGTGGATTGAAATGGATATCTTTAGAGAAGCAGCGAGGTCTCGATTATGTCGCTCCTTATGTAGGAGCGTGGATTGAAATTTTAATGACTCACGACTAAATGAAATGTGGGCTTGTCGCTCCTTATGTAGGAGCGTGGATTGAAAT

>NZ_LN831776|24|25|1619873-1621568|CRISPRCasFinder
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CATTCGAAAATTTTTTTGAAGCGGAGTGTCTTT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATCACGTTTGCGACCGTTAGCTGCGTGTGCTGATC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ATTTTCCCGGCATCCATAGCAAACCTCCTGAATA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TTACTGTGAATAAACGGTATGTCAACCCTATGGA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ATATTCAGATTGTTCCTTCGCAAATTTCTCCCGCT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ATCGTCAGCAGCATCCACAATCGTAGATGGTCTT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TCCACGTTGCCCCATCCGTGATACGGAGACTTACCG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TAACGCCGGGTGCAGCAACACGCTGCGGGTACAT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCCGTTTATGCTGATATACGTGTCGATTGCTTAC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ACATTCTTCCCGGGATGCAGCAGCGTGCCGGTGTG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TACATCTCTTTCTTGGTCAGGCCCGAAAACAAT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CAGAGGATATAATCGATCTGCACTAGACGGTCGT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CCTCCTACGTATGCTGGGGGGCTAATCTGTACA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CCCTGGAGGATGTGAACAAGTTTTTGGACATTCGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCGATTACATAATACTGCCGTACTTAGAGGAGATG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TTATCCCTCCCGTGTATGCTCGCCGGTATTTAAGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ACAGTATGCAGTGATAGAAAGTAGCCCAACCGCC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TGATAAAAGTCACATTCAAAGCCAGCTGCCTTCAG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CATGACAAGGATGGACTTGCCGCGTCCGGATCGCGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	AGTGATATTACCATACTCATCGCGGGCACGTAAA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCTCGATTAACGCCATCTGCGCCGTAATCCGTAGC
GTTGCTCCTTATACAGGAGCGTGGATTGAAAT	AAAACTCGGGTTTAGTGCAGACCAGATGTTTGAT
GTCGCTTCTTATGTAGGAGCGTGGATTGAAAT	AATACAAACAACATCATTGAGAAAAGGTTAATTCC
GTCGCTCCTTATGCAGGAGCGTGGATTGAAAT	AAGCTGATCGTCAGTAGCCTCCTGCACAGCACTGA
GTCGCTCCTTATGTGGGGGCGTGGATCGAAAT	CCCTTAACTAGAGACGTTATGCGCACAGAGATCAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAATCGCTGGCGATTTTAGCGGCCTCCAGATCAATCTTGTCGCTCCTTATGTAGAGCGTGGATTAAATGGCAAGGACCGGGAAGGAAAAGCCGTCGCGGAAGGTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	CCTGTGTCGTCCTTTGCTAGTGCGGAAGATTGGAC
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	ATTGCAACGATCTCTACGATGCTCGGTCCGTA
GTCGCTCCTTATGCAGGAGCGTGGATTGAAAT	AAGGACAAACTGTTTGAACGCGATTTGCGAGAT
GTCGCTCTTTATGTAGGAGCGTGGATTGAAAT	GGATATCTTTAGAGAAGCAGCGAGGTCTCGATTAT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	TTTAATGACTCACGACTAAATGAAATGTGGGCTT


>NZ_LN831776|24|4|1619873-1622026|CRT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CATTCGAAAATTTTTTTGAAGCGGAGTGTCTTT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATCACGTTTGCGACCGTTAGCTGCGTGTGCTGATC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ATTTTCCCGGCATCCATAGCAAACCTCCTGAATA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TTACTGTGAATAAACGGTATGTCAACCCTATGGA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ATATTCAGATTGTTCCTTCGCAAATTTCTCCCGCT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ATCGTCAGCAGCATCCACAATCGTAGATGGTCTT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TCCACGTTGCCCCATCCGTGATACGGAGACTTACCG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TAACGCCGGGTGCAGCAACACGCTGCGGGTACAT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCCGTTTATGCTGATATACGTGTCGATTGCTTAC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ACATTCTTCCCGGGATGCAGCAGCGTGCCGGTGTG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TACATCTCTTTCTTGGTCAGGCCCGAAAACAAT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CAGAGGATATAATCGATCTGCACTAGACGGTCGT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CCTCCTACGTATGCTGGGGGGCTAATCTGTACA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CCCTGGAGGATGTGAACAAGTTTTTGGACATTCGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCGATTACATAATACTGCCGTACTTAGAGGAGATG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TTATCCCTCCCGTGTATGCTCGCCGGTATTTAAGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ACAGTATGCAGTGATAGAAAGTAGCCCAACCGCC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TGATAAAAGTCACATTCAAAGCCAGCTGCCTTCAG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CATGACAAGGATGGACTTGCCGCGTCCGGATCGCGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	AGTGATATTACCATACTCATCGCGGGCACGTAAA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCTCGATTAACGCCATCTGCGCCGTAATCCGTAGC
GTTGCTCCTTATACAGGAGCGTGGATTGAAAT	AAAACTCGGGTTTAGTGCAGACCAGATGTTTGAT
GTCGCTTCTTATGTAGGAGCGTGGATTGAAAT	AATACAAACAACATCATTGAGAAAAGGTTAATTCC
GTCGCTCCTTATGCAGGAGCGTGGATTGAAAT	AAGCTGATCGTCAGTAGCCTCCTGCACAGCACTGA
GTCGCTCCTTATGTGGGGGCGTGGATCGAAAT	CCCTTAACTAGAGACGTTATGCGCACAGAGATCAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	CGCTGGCGATTTTAGCGGCCTCCAGATCAATCTT
GTCGCTCCTTATGTAGAGCGTGGATTAAATGG	CAAGGACCGGGAAGGAAAAGCCGTCGCGGAAG
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	CCTGTGTCGTCCTTTGCTAGTGCGGAAGATTGGAC
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	ATTGCAACGATCTCTACGATGCTCGGTCCGTA
GTCGCTCCTTATGCAGGAGCGTGGATTGAAAT	AAGGACAAACTGTTTGAACGCGATTTGCGAGAT
GTCGCTCTTTATGTAGGAGCGTGGATTGAAAT	GGATATCTTTAGAGAAGCAGCGAGGTCTCGATTAT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	TTTAATGACTCACGACTAAATGAAATGTGGGCTT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT

>NZ_LN831776|24|5|1620005-1620174|PILER-CR
GTCGCTCCTTATACAGGAGCGTGGATTGAAATATTTTCC	CGGCATCCATAGCAAACCTCCTGAATA
GTCGCTCCTTATACAGGAGCGTGGATTGAAATTTACTGT	GAATAAACGGTATGTCAACCCTATGGAGTCGCT
CCTTATACAGGAGCGTGGATTGAAATATATTCAGATTGTTCCTTCGCAAATTTCTCCCGCTGTCGCTCCTTATACAGGAGCGTGGATTGAAATATCGTCAGCAGCATCCACAATCGTAGATGGTCTTGTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TCCACGTTGCCCCATCCGTGATACGGAGACTTACCG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TAACGCCGGGTGCAGCAACACGCTGCGGGTACAT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCCGTTTATGCTGATATACGTGTCGATTGCTTAC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ACATTCTTCCCGGGATGCAGCAGCGTGCCGGTGTG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TACATCTCTTTCTTGGTCAGGCCCGAAAACAAT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CAGAGGATATAATCGATCTGCACTAGACGGTCGT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CCTCCTACGTATGCTGGGGGGCTAATCTGTACA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CCCTGGAGGATGTGAACAAGTTTTTGGACATTCGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCGATTACATAATACTGCCGTACTTAGAGGAGATG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TTATCCCTCCCGTGTATGCTCGCCGGTATTTAAGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ACAGTATGCAGTGATAGAAAGTAGCCCAACCGCC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TGATAAAAGTCACATTCAAAGCCAGCTGCCTTCAG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CATGACAAGGATGGACTTGCCGCGTCCGGATCGCGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	AGTGATATTACCATACTCATCGCGGGCACGTAAA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCTCGATTAACGCCATCTGCGCCGTAATCCGTAGC
GTTGCTCCTTATACAGGAGCGTGGATTGAAAT	AAAACTCGGGTTTAGTGCAGACCAGATGTTTGAT
GTCGCTTCTTATGTAGGAGCGTGGATTGAAATAATACAAACAACATCATTGAGAAAAGGTTAATTCCGTCGCTCCTTATGCAGGAGCGTGGATTGAAATAAGCTGATCGTCAGTAGCCTCCTGCACAGCACTGAGTCGCTCCTTATGTGGGGGCGTGGATCGAAATCCCTTAACTAGAGACGTTATGCGCACAGAGATCAGTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCGCTGGCGATTTTAGCGGCCTCCAGATCAATCTTGTCGCTCCTTATGTAGAGCGTGGATTAAATGGCAAGGACCGGGAAGGAAAAGCCGTCGCGGAAGGTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	CCTGTGTCGTCCTTTGCTAGTGCGGAAGATTGGAC
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	ATTGCAACGATCTCTACGATGCTCGGTCCGTA
GTCGCTCCTTATGCAGGAGCGTGGATTGAAAT	AAGGACAAACTGTTTGAACGCGATTTGCGAGAT
GTCGCTCTTTATGTAGGAGCGTGGATTGAAAT	GGATATCTTTAGAGAAGCAGCGAGGTCTCGATTAT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	TTTAATGACTCACGACTAAATGAAATGTGGGCTT


>NZ_LN831776|24|6|1620270-1621365|PILER-CR
	CGGCATCCATAGCAAACCTCCTGAATA
GTCGCTCCTTATACAGGAGCGTGGATTGAAATTTACTGT	GAATAAACGGTATGTCAACCCTATGGAGTCGCT
CCTTATACAGGAGCGTGGATTGAAATATATTCAGATTGTTCCTTCGCAAATTTCTCCCGCTGTCGCTCCTTATACAGGAGCGTGGATTGAAATATCGTCAGCAGCATCCACAATCGTAGATGGTCTTGTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TCCACGTTGCCCCATCCGTGATACGGAGACTTACCG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TAACGCCGGGTGCAGCAACACGCTGCGGGTACAT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCCGTTTATGCTGATATACGTGTCGATTGCTTAC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ACATTCTTCCCGGGATGCAGCAGCGTGCCGGTGTG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TACATCTCTTTCTTGGTCAGGCCCGAAAACAAT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CAGAGGATATAATCGATCTGCACTAGACGGTCGT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CCTCCTACGTATGCTGGGGGGCTAATCTGTACA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CCCTGGAGGATGTGAACAAGTTTTTGGACATTCGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCGATTACATAATACTGCCGTACTTAGAGGAGATG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TTATCCCTCCCGTGTATGCTCGCCGGTATTTAAGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ACAGTATGCAGTGATAGAAAGTAGCCCAACCGCC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TGATAAAAGTCACATTCAAAGCCAGCTGCCTTCAG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CATGACAAGGATGGACTTGCCGCGTCCGGATCGCGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	AGTGATATTACCATACTCATCGCGGGCACGTAAA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCTCGATTAACGCCATCTGCGCCGTAATCCGTAGC
GTTGCTCCTTATACAGGAGCGTGGATTGAAAT	AAAACTCGGGTTTAGTGCAGACCAGATGTTTGAT
GTCGCTTCTTATGTAGGAGCGTGGATTGAAATAATACAAACAACATCATTGAGAAAAGGTTAATTCCGTCGCTCCTTATGCAGGAGCGTGGATTGAAATAAGCTGATCGTCAGTAGCCTCCTGCACAGCACTGAGTCGCTCCTTATGTGGGGGCGTGGATCGAAATCCCTTAACTAGAGACGTTATGCGCACAGAGATCAGTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCGCTGGCGATTTTAGCGGCCTCCAGATCAATCTTGTCGCTCCTTATGTAGAGCGTGGATTAAATGGCAAGGACCGGGAAGGAAAAGCCGTCGCGGAAGGTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	CCTGTGTCGTCCTTTGCTAGTGCGGAAGATTGGAC
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	ATTGCAACGATCTCTACGATGCTCGGTCCGTA
GTCGCTCCTTATGCAGGAGCGTGGATTGAAAT	AAGGACAAACTGTTTGAACGCGATTTGCGAGAT
GTCGCTCTTTATGTAGGAGCGTGGATTGAAAT	GGATATCTTTAGAGAAGCAGCGAGGTCTCGATTAT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	TTTAATGACTCACGACTAAATGAAATGTGGGCTT


>NZ_LN831776|24|7|1621666-1622026|PILER-CR
	CGGCATCCATAGCAAACCTCCTGAATA
GTCGCTCCTTATACAGGAGCGTGGATTGAAATTTACTGT	GAATAAACGGTATGTCAACCCTATGGAGTCGCT
CCTTATACAGGAGCGTGGATTGAAATATATTCAGATTGTTCCTTCGCAAATTTCTCCCGCTGTCGCTCCTTATACAGGAGCGTGGATTGAAATATCGTCAGCAGCATCCACAATCGTAGATGGTCTTGTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TCCACGTTGCCCCATCCGTGATACGGAGACTTACCG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TAACGCCGGGTGCAGCAACACGCTGCGGGTACAT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCCGTTTATGCTGATATACGTGTCGATTGCTTAC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ACATTCTTCCCGGGATGCAGCAGCGTGCCGGTGTG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TACATCTCTTTCTTGGTCAGGCCCGAAAACAAT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CAGAGGATATAATCGATCTGCACTAGACGGTCGT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CCTCCTACGTATGCTGGGGGGCTAATCTGTACA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CCCTGGAGGATGTGAACAAGTTTTTGGACATTCGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCGATTACATAATACTGCCGTACTTAGAGGAGATG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TTATCCCTCCCGTGTATGCTCGCCGGTATTTAAGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ACAGTATGCAGTGATAGAAAGTAGCCCAACCGCC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TGATAAAAGTCACATTCAAAGCCAGCTGCCTTCAG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CATGACAAGGATGGACTTGCCGCGTCCGGATCGCGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	AGTGATATTACCATACTCATCGCGGGCACGTAAA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCTCGATTAACGCCATCTGCGCCGTAATCCGTAGC
GTTGCTCCTTATACAGGAGCGTGGATTGAAAT	AAAACTCGGGTTTAGTGCAGACCAGATGTTTGAT
GTCGCTTCTTATGTAGGAGCGTGGATTGAAATAATACAAACAACATCATTGAGAAAAGGTTAATTCCGTCGCTCCTTATGCAGGAGCGTGGATTGAAATAAGCTGATCGTCAGTAGCCTCCTGCACAGCACTGAGTCGCTCCTTATGTGGGGGCGTGGATCGAAATCCCTTAACTAGAGACGTTATGCGCACAGAGATCAGTGTCGCTCCTTATGTGGGAGCGTGGATTGAAATCGCTGGCGATTTTAGCGGCCTCCAGATCAATCTTGTCGCTCCTTATGTAGAGCGTGGATTAAATGGCAAGGACCGGGAAGGAAAAGCCGTCGCGGAAGGTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	CCTGTGTCGTCCTTTGCTAGTGCGGAAGATTGGAC
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	ATTGCAACGATCTCTACGATGCTCGGTCCGTA
GTCGCTCCTTATGCAGGAGCGTGGATTGAAAT	AAGGACAAACTGTTTGAACGCGATTTGCGAGAT
GTCGCTCTTTATGTAGGAGCGTGGATTGAAAT	GGATATCTTTAGAGAAGCAGCGAGGTCTCGATTAT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	TTTAATGACTCACGACTAAATGAAATGTGGGCTT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT

>NZ_LN831776|24|26|1621666-1622026|CRISPRCasFinder
	CATTCGAAAATTTTTTTGAAGCGGAGTGTCTTT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAAT	ATCACGTTTGCGACCGTTAGCTGCGTGTGCTGATC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ATTTTCCCGGCATCCATAGCAAACCTCCTGAATA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TTACTGTGAATAAACGGTATGTCAACCCTATGGA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ATATTCAGATTGTTCCTTCGCAAATTTCTCCCGCT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ATCGTCAGCAGCATCCACAATCGTAGATGGTCTT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TCCACGTTGCCCCATCCGTGATACGGAGACTTACCG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TAACGCCGGGTGCAGCAACACGCTGCGGGTACAT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCCGTTTATGCTGATATACGTGTCGATTGCTTAC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ACATTCTTCCCGGGATGCAGCAGCGTGCCGGTGTG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TACATCTCTTTCTTGGTCAGGCCCGAAAACAAT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CAGAGGATATAATCGATCTGCACTAGACGGTCGT
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CCTCCTACGTATGCTGGGGGGCTAATCTGTACA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CCCTGGAGGATGTGAACAAGTTTTTGGACATTCGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCGATTACATAATACTGCCGTACTTAGAGGAGATG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TTATCCCTCCCGTGTATGCTCGCCGGTATTTAAGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	ACAGTATGCAGTGATAGAAAGTAGCCCAACCGCC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	TGATAAAAGTCACATTCAAAGCCAGCTGCCTTCAG
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	CATGACAAGGATGGACTTGCCGCGTCCGGATCGCGC
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	AGTGATATTACCATACTCATCGCGGGCACGTAAA
GTCGCTCCTTATACAGGAGCGTGGATTGAAAT	GCTCGATTAACGCCATCTGCGCCGTAATCCGTAGC
GTTGCTCCTTATACAGGAGCGTGGATTGAAAT	AAAACTCGGGTTTAGTGCAGACCAGATGTTTGAT
GTCGCTTCTTATGTAGGAGCGTGGATTGAAAT	AATACAAACAACATCATTGAGAAAAGGTTAATTCC
GTCGCTCCTTATGCAGGAGCGTGGATTGAAAT	AAGCTGATCGTCAGTAGCCTCCTGCACAGCACTGA
GTCGCTCCTTATGTGGGGGCGTGGATCGAAAT	CCCTTAACTAGAGACGTTATGCGCACAGAGATCAGT
GTCGCTCCTTATGTGGGAGCGTGGATTGAAATCGCTGGCGATTTTAGCGGCCTCCAGATCAATCTTGTCGCTCCTTATGTAGAGCGTGGATTAAATGGCAAGGACCGGGAAGGAAAAGCCGTCGCGGAAGGTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	CCTGTGTCGTCCTTTGCTAGTGCGGAAGATTGGAC
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	ATTGCAACGATCTCTACGATGCTCGGTCCGTA
GTCGCTCCTTATGCAGGAGCGTGGATTGAAAT	AAGGACAAACTGTTTGAACGCGATTTGCGAGAT
GTCGCTCTTTATGTAGGAGCGTGGATTGAAAT	GGATATCTTTAGAGAAGCAGCGAGGTCTCGATTAT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT	TTTAATGACTCACGACTAAATGAAATGTGGGCTT
GTCGCTCCTTATGTAGGAGCGTGGATTGAAAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020426227.1|1624132_1624627_+|DinB-family-protein	unknown	unknown	gnl|CDD|378981
NZ_LN831776.1|WP_039785559.1|1627470_1628223_+|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|225130
NZ_LN831776.1|WP_052741421.1|1601927_1602917_+|hypothetical-protein	PD-DExK	mkCas0090_PD-DExK_CAS-I:CAS-III	unknown
NZ_LN831776.1|WP_046501633.1|1618215_1619322_-|linear-amide-C-N-hydrolase	unknown	unknown	gnl|CDD|367486
NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	gnl|CDD|273847
NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	gnl|CDD|187887
NZ_LN831776.1|WP_020426224.1|1625250_1625610_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_167330838.1|1624773_1624944_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	gnl|CDD|224124
NZ_LN831776.1|WP_020426223.1|1625730_1626216_+|SprT-family-protein	unknown	unknown	gnl|CDD|235290
NZ_LN831776.1|WP_020431498.1|1613466_1613757_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl|CDD|187856
NZ_LN831776.1|WP_020431500.1|1612425_1613457_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	gnl|CDD|188360
NZ_LN831776.1|WP_039785553.1|1626910_1627339_-|Lrp/AsnC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224439
NZ_LN831776.1|WP_046501636.1|1623299_1623869_-|CGNR-zinc-finger-domain-containing-protein	unknown	unknown	gnl|CDD|378696
NZ_LN831776.1|WP_020431502.1|1611772_1612429_+|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl|CDD|224385
NZ_LN831776.1|WP_046501630.1|1617329_1618190_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|197666
NZ_LN831776.1|WP_020426225.1|1625027_1625165_-|cortex-morphogenetic-protein-CmpA	unknown	unknown	gnl|CDD|380221
NZ_LN831776.1|WP_020426222.1|1626224_1626878_-|pentapeptide-repeat-containing-protein	unknown	unknown	gnl|CDD|224276
NZ_LN831776.1|WP_020426229.1|1622135_1623242_+|GGDEF-domain-containing-protein	unknown	unknown	gnl|CDD|143635
NZ_LN831776.1|WP_020431504.1|1610922_1611783_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	COG3649_cas7_CAS-I-C	gnl|CDD|187820

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831776.1|WP_020431498.1|1613466_1613757_+|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	1.1e-31	103.6	1.1
NZ_LN831776.1|WP_020431500.1|1612425_1613457_+|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	3.4e-146	481.3	0.2
NZ_LN831776.1|WP_052741421.1|1601927_1602917_+|hypothetical-protein	PD-DExK	mkCas0090_PD-DExK_CAS-I:CAS-III	8.9e-27	87.9	0.3
NZ_LN831776.1|WP_020431504.1|1610922_1611783_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	COG3649_cas7_CAS-I-C	2.3e-127	418.8	0.8
NZ_LN831776.1|WP_020431502.1|1611772_1612429_+|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	9.6e-35	114.8	1.6
NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	7.7e-161	531.0	1.6
NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	3.3e-85	281.5	7.6
NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	1e-60	199.7	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020426227.1|1624132_1624627_+|DinB-family-protein	gnl|CDD|378981	pfam12867, DinB_2, DinB superfamily. The DinB family are an uncharacterized family of potential enzymes. The structure of these proteins is composed of a four helix bundle.	3.53876e-08
NZ_LN831776.1|WP_039785559.1|1627470_1628223_+|MBL-fold-metallo-hydrolase	gnl|CDD|225130	COG2220, COG2220, Predicted Zn-dependent hydrolases of the beta-lactamase fold [General function prediction only].	6.536e-13
NZ_LN831776.1|WP_020426225.1|1625027_1625165_-|cortex-morphogenetic-protein-CmpA	gnl|CDD|380221	NF033225, spore_CmpA, cortex morphogenetic protein CmpA. Members of this family are CmpA (cortex morphogenetic protein A), a small protein (37 amino acids) involved in endospore formation and frequently missed during genome annotation.	1.76744e-17
NZ_LN831776.1|WP_046501633.1|1618215_1619322_-|linear-amide-C-N-hydrolase	gnl|CDD|367486	pfam03417, AAT, Acyl-coenzyme A:6-aminopenicillanic acid acyl-transferase.	1.24319e-30
NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5	gnl|CDD|273847	TIGR01876, cas_Cas5d, CRISPR-associated protein Cas5, subtype I-C/DVULG. CRISPR is a term for Clustered, Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This small Cas family is represented by CT1134 of Chlorobium tepidum. This family belongs to a set of several Cas protein families, one each for a number of different CRISPR/Cas subtypes, that share a region of N-terminal sequence similarity modeled by TIGR02593. This family represents the Dvulg subtype of CRISPR/Cas locus.	3.09357e-90
NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	gnl|CDD|187887	cd09757, Cas8c_I-C, CRISPR/Cas system-associated protein Cas8c. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Zn-finger domain containing protein, distant homologs of Cas8 proteins; signature gene for I-C subtype; also known as Csd1 family.	2.89947e-169
NZ_LN831776.1|WP_020426222.1|1626224_1626878_-|pentapeptide-repeat-containing-protein	gnl|CDD|224276	COG1357, COG1357, Pentapeptide repeats containing protein [Function unknown].	2.22208e-16
NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3	gnl|CDD|224124	COG1203, COG1203, CRISPR-associated helicase Cas3 [Defense mechanisms].	7.24875e-69
NZ_LN831776.1|WP_020426223.1|1625730_1626216_+|SprT-family-protein	gnl|CDD|235290	PRK04351, PRK04351, SprT family protein.	4.70474e-78
NZ_LN831776.1|WP_020431498.1|1613466_1613757_+|CRISPR-associated-endonuclease-Cas2	gnl|CDD|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	1.93294e-34
NZ_LN831776.1|WP_020431500.1|1612425_1613457_+|type-I-C-CRISPR-associated-endonuclease-Cas1	gnl|CDD|188360	TIGR03640, cas1_DVULG, CRISPR-associated endonuclease Cas1, subtype I-C/DVULG. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes the Cas1 protein particular to the DVULG subtype of CRISPR/Cas system.	0
NZ_LN831776.1|WP_039785553.1|1626910_1627339_-|Lrp/AsnC-family-transcriptional-regulator	gnl|CDD|224439	COG1522, Lrp, Transcriptional regulators [Transcription].	4.58678e-26
NZ_LN831776.1|WP_020426229.1|1622135_1623242_+|GGDEF-domain-containing-protein	gnl|CDD|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	2.76115e-51
NZ_LN831776.1|WP_020431502.1|1611772_1612429_+|CRISPR-associated-protein-Cas4	gnl|CDD|224385	COG1468, COG1468, CRISPR-associated protein Cas4 (RecB family exonuclease) [Defense mechanisms].	1.41191e-27
NZ_LN831776.1|WP_046501630.1|1617329_1618190_-|helix-turn-helix-domain-containing-protein	gnl|CDD|197666	smart00342, HTH_ARAC, helix_turn_helix, arabinose operon control protein.	5.79213e-25
NZ_LN831776.1|WP_046501636.1|1623299_1623869_-|CGNR-zinc-finger-domain-containing-protein	gnl|CDD|378696	pfam11706, zf-CGNR, CGNR zinc finger. This family consists of a C-terminal zinc finger domain. It seems likely to be DNA-binding given the conservation of many positively charged residues. The domain is named after a highly conserved motif found in many members of the family.	1.66574e-19
NZ_LN831776.1|WP_020431504.1|1610922_1611783_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2	gnl|CDD|187820	cd09689, Cas7_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas7. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas7 is a RAMP superfamily protein; Subunit of the Cascade complex; also known as Csd2 family.	9.02891e-134

Protein sequences

>NZ_LN831776.1|WP_046501633.1|1618215_1619322_-|linear-amide-C-N-hydrolase
MEKTKVYFKNFIGTSYEVGTEIGQWVLSTPSLLKQVLLPPNAYPNDKFTKITDLLDRYCQGINEEIKGFADTIGVSSEQALFYTMTYLERGCSLMAVLPSKSKSGHTLMARNYDFNNEMEEMCFAFTNIKGKYRYIGSTLNLFGRCDGMNEHGLAVCKASNGVPVGNFEGGQKAGATGFSFWVVVRSILENCKTVQEAIEWTMSAPIGYNMNLMLADSSNKIALLQCMDGHKSYKLLDEYSEEAFLSVTNHAVLEDIKPYQKMIIENSVVRNNKIVEVFTGKKQLSKKDMKTLLSTSYPDGLCCHYYKEFFGTLRSMIFDVNDKTIEMTFGSPQVNEWQTFSVGALEMQEVEVLLPQEKARPDFYKIS
>NZ_LN831776.1|WP_046501630.1|1617329_1618190_-|helix-turn-helix-domain-containing-protein
MINNRAIGEAIVFIENSLYEPIAACDVAKAVSYSYYHFHRYFQAIMGETIGSYIRTRRLTQAAWDLVHSEKKILDIGVSLYFETAESFTRAFKDRYGMTPTEYRKNGIDVLIGNRPPAQISDNIVHPYADLSPQIVTVPETYTMGIRFITTISRNESIAMWQLFNQQIPDTFAGTRYGIFEAGETCAADVFNPQSETTAFVGIEFPKEQPILRGMERKTIRGGKYARFIHKGIVKDLMQTYHYIWGVWFPKSGYELDNRDDFECYTERFAGENIESSEIDIYFPIK
>NZ_LN831776.1|WP_020431498.1|1613466_1613757_+|CRISPR-associated-endonuclease-Cas2
MLVVITYDVSTLSGEGQSRLRKVSKICQNYGQRVQNSVFECVVDAAQFAELKIKLKTIIDDDEDSIRFYQLGNNHKNKVEHVGIKKSIDLEGPLIL
>NZ_LN831776.1|WP_020431500.1|1612425_1613457_+|type-I-C-CRISPR-associated-endonuclease-Cas1
MKKLLNTLYITQPSVYLSLDGDNVVLLKEEEKLGRFPLHNLESIVTFGYTGASPALMGYCADSNISLLFLTMNGRYLARVTGQSRGNVVLRKKQYNLSEDEVRSAKIARNFIIGKIYNHKWMLERMTRDYPLRVNVELFKETSQQLSSLILEVRACEQLDRLRGLEGQAAATYYSQFNQMILQQKEDFYFHSRTRRPPLDNVNAMLSLAYTLLTHDTASALEAVGLDAYVGFLHRDRPGRVSLALDVMEELRGVFADKFVLTLINKKLISKADFLKKENGAVIMTDEARKKFLAAWQSKKQETITHPYLGEKISWGLVPHAQALLLARHLRNDLDEYPPFLWK
>NZ_LN831776.1|WP_020431502.1|1611772_1612429_+|CRISPR-associated-protein-Cas4
MEYDDEDELMLSGIQHFHFCKRQWALIHIEQQWEENVRTIEGQHLHRNADQPLIREKRVDKIIVRAMPVKSRELNISGICDVVEFIRDDSGVEINGADGKYAAYPVEYKRGKPKREDEDILQLAAQAMCLEEMLLCEVSTGYIFYNEIKHRIEVPLTAELKANVKAIVEVMQSYYHRRHTPKVKTGPFCKSCSLQHICLPKLMNKQSVKSYVEGKIRE
>NZ_LN831776.1|WP_020431504.1|1610922_1611783_+|type-I-C-CRISPR-associated-protein-Cas7/Csd2
MTILDHKIDFAVIVSVTKANPNGDPLNGNRPRQNYDGYGEISDVALKRKIRNRLQDMGESIFVQSNDRKSDSYNSLRERADANAELDKILKAKGSSNEEFARIACQEWLDVRSFGQVFAFKADKGAGVSVGVRGPVSIHTATSVSPIDITSMQITKSVNSEPGKDRGSDTMGMKHRVDFGVYVFYGSINTQLAEKTGFSNEDAEKIKQVLVTLFENDASAARPDGSMEVHKVYWWEHNSKLGQYSSAKVHRSLVVRPKVDDPKTIADYEIVVSEMEGLKAEVIDGI
>NZ_LN831776.1|WP_020431505.1|1609011_1610919_+|type-I-C-CRISPR-associated-protein-Cas8c/Csd1
MSWLLNLYETYQSNQDCVGVIETRYNDREYTLLPVSHTTQNAHIEVNVTEDGEFHSASVLDKSESSTLIPCTEDSASRAGSKVAPYPLHDKLSYVAGDFLAYGGKIKKEEPFAAYIKQLGGWADSPYACPKVKSIHSYLSKRRLIQDLVSHSILFLDADHQLIEKWDKKYEALHGEKPLIFSAVAGEQESAFIRFNVYSPDKELTKVWKDPEMYDSFMQYYSHLLGQEDYCYVTGRMLPSTDRHANKIRNAADKAKLISSNDTSGFTFRGRFTQSSDAASISYEVSQKAHNALKWLINRQGKIVDQRVFLVWGNDDLNIPDPTEDFFSFDLEPAVARERKSYTHKEYAGEIAKAMDGYRNKLASEYKSDVNILVLDSATTGRLAVLYYRNMDKQLYLDKLVHWHSTCSWLHRYRKNTQDEWVEFYGASATKDIAFAAYGPKANEKIVKGVMERLLPCIVDGHNIPQDIVRSAFYRASNPVSMEKWEWEKTLSITCALINAKEEMNVALDTEIDDRSYLFGRLLAIADVLERRALDSDEKRSTNAIRYMNAFSQHPERTWNTIQQSIQPHQARLGTKLRYYSSLIDEVASKIPLDQFNNKPLSGKYLLGFYSQRHELYQKKDKNNDSIQASENGER
>NZ_LN831776.1|WP_020431506.1|1608295_1609015_+|type-I-C-CRISPR-associated-protein-Cas5
MRNSIEFKVYGKYALFTDPLTKLGGEKLTYSVPTYQALKGIVESIYWKPTIHIIVEEVRIMNAIRMESKGIRPMDYGGGNTLANYTYLKDVCYEVRAHFEFNMNRPDLEHDRNEHKHHNLLKRSLQAGGRRDIFLGARECQAYVEPCVFGVERGFYNDYGDIHLGSMVHGINYPDETGRDEMEVRLWSPVMRDGIIRFIRPEECTQVRRIAEMKPKSFNETNLQTAEELLAQIEAEEKA
>NZ_LN831776.1|WP_020431507.1|1605728_1608185_+|CRISPR-associated-helicase/endonuclease-Cas3
MEYIAHIRESDMKVQTVTEHLLEVRTLAEKYGKKLGIKYMAGLAGMLHDLGKYTEEFRNYIVQAVYHPEAPPSRGSVDHSTAGGKLLFERFHRVPADLSNKEAHINKMILAEVVGNAILSHHSYLQDFLNPDSESNFLNRVQDKCLPEFERAKDSFFELVMNETEFHLYVDKAVEELSDYLKVDSSSTTELKLMFLTKYVFSALIDADRTNTRCFEENQPDPSYNPQQLFSAYYTKLMTKIDSFHNHKHAHSAINQLRQGMSEQCEQFAAEPSGIYTLSIPTGGGKTLASLRYALKHALLKEKKHIIYVVPYTTIIEQNANEIRSILKDDEHILEHHSNVVEEETQDDEHEDGSLSLRQKLKLAKDNWDAPIIFTTMVQFLNVFYADGSRNIRRLHNLSESVIVFDEVQKVPVRCVSLFNQALNFLKSYAHSSIVLCTATQPELDYVRLKLEIEPEAEMIHNLDHVIEAFRRVEIVDRATNEHFDNDTLTEFVITQMREVSSVLVILNTKSVVQALYRSLNERNLSVPIYHLSTSMCAAHRNQILDKVKALLEDKEPVICISTQLIEAGVDVSFQCVIRSLAGLDSIAQAAGRCNRHGEDLIRQVYVIDHIEENLKHLKEIKIGKEISRKILIDLSRDASLHGGHILSIQAMEKYFKEFYTELATSLNYSIPKLGQEMTTLLSGPRKNNAYYQAYLSKHRAALPLFLLNSYKTAAENFQVIDNLTTTVVVPFGDGPEEGKDIIAELNGQQSIPDLTRLLRKAQQYTINIYSYEKDLLSKNGSLVPYLDGKILALKEGAYHPEYGLNLENDSPLDMYMF
>NZ_LN831776.1|WP_052741421.1|1601927_1602917_+|hypothetical-protein
MKDKQPSSEQELEEMRKAAPKIIQQIAQNYIHLEESITSQLRMAAGSHHVTSGTFREDIWKSLFEQIIPRKFSIEQSVFIIDSHGLVSKEVDLAIFDEQYTPYIFRLGRIKYIPIEAVAVVVQCKSNNIHGRNKRENLRTWSKSITNLKTSLKSVARIHTGIAKGEYDYILDKDGQLRIEPEKLEKSDRDKLAQTSTRPIQILCHTKDTSSSKYDDLFDIVIHPEGERLRVEMKPDLKDLPSWYDSLNHKQDPRYEHIVKPFDTKEPSEDFQKALQVDNYKVYKDKARTKEIGLLSLTFQLNQLLMLINNPILFPHMAYVDMFNTNISK
>NZ_LN831776.1|WP_020426229.1|1622135_1623242_+|GGDEF-domain-containing-protein
MSPSGTSAYRQAKWIKRFLQTYWLVIALHFLAQLAAYTFLPYERGAHEFYYGVLLYPTLLMGAVVGIAQWIDRRASKYSFISLFMAGTIIAMIIIHLNMDIRIIGALMLLPIFASAIFYRLDLTFFTFALQAVAFFVMYRWDYWFKYFFSSFDLIAIPIFLVVGTLVASIMIINGRELVSDLEASLMAKQDLLIENAVMRKLSTTDALTDLYNHISFHEFYDKALEYGDQGAPFHLALIDIDNFKLINDKYGHRAGDIILARVAKVIRDLISSADIAARYGGEEFAILFFEKTFEEAEAIADKIRLRLSGTPHEEMDGAAVTVSIGLKSYSQGTTKEQLFEEVDALLYAAKHEGKNKVRTPYSSTVFT
>NZ_LN831776.1|WP_046501636.1|1623299_1623869_-|CGNR-zinc-finger-domain-containing-protein
MLWDDFINSYWRDWRTGDRSKDKDKLQDQEWLAVWLEQHSLRAELPPEPKELEQLQQLRSLLREAVQKLVQDCPPDGDLLERLNGYMLMGPVIRQVVQSVEGKVKISFQPQRPDWEQVMAEIASSFAAALVEKDTSRFRICENPDCLWVYYDDTRNRSKRYCDDKMCGNLMKVRRFRARKKAGMEGNSE
>NZ_LN831776.1|WP_020426227.1|1624132_1624627_+|DinB-family-protein
MQNKISDVLLQNWDYVMDIEDWAPPLSAALEGVTSEQAVWKPQGEAGNSIWETVNHLTYYKERLLIKLKGLPKLPEAESNDATFTVTESGEEAWGHAVAKLKQVHASLREVIEALEEGAYDWGGSGHAPGEEVMSLILHDSYHTGQIVLVRKLQGSWPTNRSFN
>NZ_LN831776.1|WP_167330838.1|1624773_1624944_+|hypothetical-protein
MMEPNYKDRSVEVERTEVQKKSDSSVVASTFIKYAAYLIIFFGLLFFLVKYVFPLF
>NZ_LN831776.1|WP_020426225.1|1625027_1625165_-|cortex-morphogenetic-protein-CmpA
MPQWLCHQLMKAYYKKDRRQIKLLNECWFFYRNSAEARDSIQREV
>NZ_LN831776.1|WP_020426224.1|1625250_1625610_-|hypothetical-protein
MPKMRYVILQQHQELQFVEMPEEYAYQLSALNLRLNKEIDKLTADNVPDLPLAIAECDSLELLREEHSLESGLAYINRLESAFSSIQESNYPLISLLTEIRALQAQLEQWYEEEEEGVH
>NZ_LN831776.1|WP_020426223.1|1625730_1626216_+|SprT-family-protein
MSNEELQQWIEQVSQDSFGVPFRHKASFNSRLSTTGGRYFIKSHNIEINPMQLEMFGREETERIIKHELCHYHLHLSKRGYMHRDADFKKLLAMVGGSRFCQTLPGAKARKPLPYRYKLVCTACATEYPRKRKADPKRYRCGNCAGKLKLVALEESRGKAK
>NZ_LN831776.1|WP_020426222.1|1626224_1626878_-|pentapeptide-repeat-containing-protein
MSNKIDPPKITEENALLPQQIHTLQSKEEISHCLISDSLIEYQEADRVSFDKVIFRNVTVTESTLHAIELTDVIFENCDLSNVNFSDAFVHRTEFRNCKLIGTDFSRGRFQNVRIVDCIGDFASFRFGKFKGTVFTNCRLVSSDYYQAELTHIGFSECDIDQATFAGCRLKEIDLSDCSFTGLHVDIEDLAGCIISAEQAASFAGLLGLVIKTDTEL
>NZ_LN831776.1|WP_039785553.1|1626910_1627339_-|Lrp/AsnC-family-transcriptional-regulator
MENYAIDDIDYRILHYIIEDSRLSHKEIGEKIHMTGQAVGARIRRMRELEIIEGYTVRWNPQKLGQNIHALITVFLSSNKAHPLFQKFALEHGSVAELHRVSGEGCYWMRVYAKDHDELATFLDQLLEFGNYRVNLGMGQLK
>NZ_LN831776.1|WP_039785559.1|1627470_1628223_+|MBL-fold-metallo-hydrolase
MKIQLIRNAALWLEYGGITFLVDPMLSEQEANPPIPNSPNARRNPLVPLPGPVQQWLAPDAVLVTHLHQDHWDEAAVSLLPHELPVLCQDGDEGTLSAQGFGHVSVVEDHAAKNFRGVTLKRTGGRHGTGEIGELMGKVSGFVFRAEGEPVLYVAGDTIWCDEVKVALDEHKPEVIIVNAGGAQFLTGGHITMNEQDIIELCRYAPEASVIAVHMEAINHCLVTREQLAARLEQEGLLGRVKIPADGEWC

Crispr_ID: NZ_LN831776_25

• CRISPR_ID: NZ_LN831776_25
• CRISPR_location: 1703430-1703506
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_25

Consensus_repeat	Method
GAGCTGAATTAGTGATCCTTTTTCCA	CRISPRCasFinder

spacers of NZ_LN831776_25

>25.1|1703456|25|NZ_LN831776|CRISPRCasFinder
CTTCGCCTGGGGAGTACAGGGTGTT

CRISPR arrays and Neighbor proteins around NZ_LN831776_25

CRISPR arrays

The CRISPR arrays of NZ_LN831776_25

>merge|NZ_LN831776|25|1703430-1703506|CRISPRCasFinder
GAGCTGAATTAGTGATCCTTTTTCCACTTCGCCTGGGGAGTACAGGGTGTTCGAGCGAATTAGTGATCCTTTTTCCA

>NZ_LN831776|25|27|1703430-1703506|CRISPRCasFinder
GAGCTGAATTAGTGATCCTTTTTCCA	CTTCGCCTGGGGAGTACAGGGTGTT
CGAGCGAATTAGTGATCCTTTTTCCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_039788062.1|1708910_1710038_+|iron-containing-alcohol-dehydrogenase-family-protein	unknown	unknown	gnl|CDD|341451
NZ_LN831776.1|WP_020428301.1|1710034_1710754_+|5'-methylthioadenosine/adenosylhomocysteine-nucleosidase	unknown	unknown	gnl|CDD|350159
NZ_LN831776.1|WP_020428314.1|1697540_1697942_-|YjbQ-family-protein	unknown	unknown	gnl|CDD|376651
NZ_LN831776.1|WP_020428305.1|1706002_1707217_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl|CDD|181219
NZ_LN831776.1|WP_020428317.1|1694667_1696023_+|glucose-6-phosphate-isomerase	unknown	unknown	gnl|CDD|184504
NZ_LN831776.1|WP_020428315.1|1696786_1697368_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_LN831776.1|WP_020428312.1|1698940_1699738_+|sulfate-ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|226665
NZ_LN831776.1|WP_020428318.1|1693515_1694418_-|NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|224995
NZ_LN831776.1|WP_039788078.1|1696150_1696783_+|YigZ-family-protein	unknown	unknown	gnl|CDD|224653
NZ_LN831776.1|WP_020428300.1|1711002_1711587_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379112
NZ_LN831776.1|WP_020428311.1|1699739_1700801_+|sulfate-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|226361
NZ_LN831776.1|WP_046501698.1|1707209_1708229_+|methionine-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|236863
NZ_LN831776.1|WP_020428306.1|1705060_1705912_+|methionine-binding-protein	unknown	unknown	gnl|CDD|270317
NZ_LN831776.1|WP_039788070.1|1700821_1701889_+|sulfate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270226
NZ_LN831776.1|WP_020428307.1|1704420_1704876_-|S-ribosylhomocysteine-lyase	unknown	unknown	gnl|CDD|179399
NZ_LN831776.1|WP_020428308.1|1703628_1704399_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|235546
NZ_LN831776.1|WP_052741422.1|1711655_1712201_+|DUF5071-domain-containing-protein	unknown	unknown	gnl|CDD|213039
NZ_LN831776.1|WP_020428309.1|1702440_1703223_+|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|293837
NZ_LN831776.1|WP_039788072.1|1698128_1698944_+|sulfate-ABC-transporter-permease-subunit-CysT	unknown	unknown	gnl|CDD|131194
NZ_LN831776.1|WP_020428303.1|1708229_1708889_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|224922

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_039788062.1|1708910_1710038_+|iron-containing-alcohol-dehydrogenase-family-protein	gnl|CDD|341451	cd08172, GlyDH-like, Glycerol_dehydrogenase-like. This family contains glycerol dehydrogenase (GlyDH)-like proteins that have yet to be characterized, but show sequence homology with glycerol dehydrogenase. Glycerol dehydrogenases (GlyDH) is a key enzyme in the glycerol dissimilation pathway. In anaerobic conditions, many microorganisms utilize glycerol as a source of carbon through coupled oxidative and reductive pathways. One of the pathways involves the oxidation of glycerol to dihydroxyacetone with the reduction of NAD+ to NADH catalyzed by glycerol dehydrogenases. Dihydroxyacetone is then phosphorylated by dihydroxyacetone kinase and enters the glycolytic pathway for further degradation. The activity of GlyDH is zinc-dependent; the zinc ion plays a role in stabilizing an alkoxide intermediate at the active site.	1.70921e-176
NZ_LN831776.1|WP_020428301.1|1710034_1710754_+|5'-methylthioadenosine/adenosylhomocysteine-nucleosidase	gnl|CDD|350159	cd09008, MTAN, 5'-methylthioadenosine/S-adenosylhomocysteine nucleosidases. This subfamily includes both bacterial and plant 5'-methylthioadenosine/S-adenosylhomocysteine (MTA/SAH) nucleosidases (MTANs): bacterial MTANs show comparable efficiency in hydrolyzing MTA and SAH, while plant enzymes are highly specific for MTA and are unable to metabolize SAH or show significantly reduced activity towards SAH. MTAN is involved in methionine and S-adenosyl-methionine recycling, polyamine biosynthesis, and bacterial quorum sensing. This subfamily belongs to the nucleoside phosphorylase-I (NP-I) family, whose members accept a range of purine nucleosides as well as the pyrimidine nucleoside uridine. The NP-1 family includes phosphorolytic nucleosidases, such as purine nucleoside phosphorylase (PNPs, EC. 2.4.2.1), uridine phosphorylase (UP, EC 2.4.2.3), and 5'-deoxy-5'-methylthioadenosine phosphorylase (MTAP, EC 2.4.2.28), and hydrolytic nucleosidases, such as AMP nucleosidase (AMN, EC 3.2.2.4), and 5'-methylthioadenosine/S-adenosylhomocysteine (MTA/SAH) nucleosidase (MTAN, EC 3.2.2.16). The NP-I family is distinct from nucleoside phosphorylase-II, which belongs to a different structural family.	1.03946e-97
NZ_LN831776.1|WP_020428314.1|1697540_1697942_-|YjbQ-family-protein	gnl|CDD|376651	pfam01894, UPF0047, Uncharacterized protein family UPF0047. This family has no known function. The alignment contains a conserved aspartate and histidine that may be functionally important.	2.25719e-61
NZ_LN831776.1|WP_020428305.1|1706002_1707217_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl|CDD|181219	PRK08068, PRK08068, transaminase; Reviewed.	0
NZ_LN831776.1|WP_020428317.1|1694667_1696023_+|glucose-6-phosphate-isomerase	gnl|CDD|184504	PRK14097, pgi, glucose-6-phosphate isomerase; Provisional.	0
NZ_LN831776.1|WP_020428315.1|1696786_1697368_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	9.55652e-17
NZ_LN831776.1|WP_020428312.1|1698940_1699738_+|sulfate-ABC-transporter-permease-subunit	gnl|CDD|226665	COG4208, CysW, ABC-type sulfate transport system, permease component [Inorganic ion transport and metabolism].	5.40082e-79
NZ_LN831776.1|WP_020428318.1|1693515_1694418_-|NAD(P)-dependent-oxidoreductase	gnl|CDD|224995	COG2084, MmsB, 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases [Lipid metabolism].	6.27542e-105
NZ_LN831776.1|WP_039788078.1|1696150_1696783_+|YigZ-family-protein	gnl|CDD|224653	COG1739, COG1739, Uncharacterized conserved protein [Function unknown].	4.91659e-68
NZ_LN831776.1|WP_020428300.1|1711002_1711587_+|GNAT-family-N-acetyltransferase	gnl|CDD|379112	pfam13302, Acetyltransf_3, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	3.93164e-25
NZ_LN831776.1|WP_020428311.1|1699739_1700801_+|sulfate-ABC-transporter-ATP-binding-protein	gnl|CDD|226361	COG3842, PotA, ABC-type spermidine/putrescine transport systems, ATPase components [Amino acid transport and metabolism].	1.42713e-132
NZ_LN831776.1|WP_046501698.1|1707209_1708229_+|methionine-ABC-transporter-ATP-binding-protein	gnl|CDD|236863	PRK11153, metN, DL-methionine transporter ATP-binding subunit; Provisional.	0
NZ_LN831776.1|WP_020428306.1|1705060_1705912_+|methionine-binding-protein	gnl|CDD|270317	cd13599, PBP2_lipoprotein_Gna1946, The membrane-associated lipoprotein Gna1946 from Neisseria meningitidis; the type 2 periplasmic binding protein fold. Gna1946 shares significant structural and sequence homology with the periplasmic substrate-binding domain of ATP-binding cassette (ABC) transporter involved in uptake of methionine (MetQ). The members of the MetQ-like family include the 32-kilodalton lipoprotein (Tp32) from Treponema pallidum, the membrane-associated lipoprotein-9 GmpC from Staphylococcus aureus, and Toll-like receptor 2-activating lipoprotein IlpA from Vibrio vulnificus. They all function as a receptor for methionine. This substrate-binding domain belongs to the type 2 periplasmic binding fold protein superfamily (PBP2). The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea.	1.0012e-136
NZ_LN831776.1|WP_039788070.1|1700821_1701889_+|sulfate-ABC-transporter-substrate-binding-protein	gnl|CDD|270226	cd01005, PBP2_CysP, Substrate binding domain of an active sulfate transporter, a member of the type 2 periplasmic binding fold superfamily. This family contains sulfate binding domain of CysP proteins that serve as initial receptors in the ABC transport of sulfate and thiosulfate in eubacteria. After binding the ligand, CysP interacts with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The CysP proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	2.78418e-118
NZ_LN831776.1|WP_020428307.1|1704420_1704876_-|S-ribosylhomocysteine-lyase	gnl|CDD|179399	PRK02260, PRK02260, S-ribosylhomocysteine lyase.	2.90689e-85
NZ_LN831776.1|WP_020428308.1|1703628_1704399_-|SDR-family-oxidoreductase	gnl|CDD|235546	PRK05653, fabG, 3-oxoacyl-ACP reductase FabG.	1.48919e-79
NZ_LN831776.1|WP_052741422.1|1711655_1712201_+|DUF5071-domain-containing-protein	gnl|CDD|213039	cd11743, Cthe_2751_like, Uncharacterized protein domain similar to Clostridium thermocellum 2751. Cthe_2751 has been found to form homodimers. Based on structural similarity to other families, a role in processing nucleic acids was suggested, though interactions with DNA could not be demonstrated.	1.86856e-32
NZ_LN831776.1|WP_020428309.1|1702440_1703223_+|MBL-fold-metallo-hydrolase	gnl|CDD|293837	cd16279, metallo-hydrolase-like_MBL-fold, uncharacterized subgroup of the MBL-fold_metallo-hydrolase superfamily; MBL-fold metallo. Members of the MBL-fold metallohydrolase superfamily are mainly hydrolytic enzymes which carry out a variety of biological functions. The class B metal beta-lactamases (MBLs) for which this fold was named perform only a small fraction of the activities included in this superfamily.Activities carried out by superfamily members include class B beta-lactamases, hydroxyacylglutathione hydrolases, AHL (acyl homoserine lactone) lactonases, persulfide dioxygenases, flavodiiron proteins, cleavage and polyadenylation specificity factors such as the Int9 and Int11 subunits of Integrator, Sdsa1-like and AtsA-like arylsulfatases, 5'-exonucleases human SNM1A and yeast Pso2p, ribonuclease J and ribonuclease Z, cyclic nucleotide phosphodiesterases, insecticide hydrolases, and proteins required for natural transformation competence. Classical members of the superfamily are di-, or less commonly mono-, zinc-ion-dependent hydrolases, however the diversity of biological roles is reflected in variations in the active site metallo-chemistry. Some members of this subgroup are named as octanoyltransferase (also known as lipoate-protein ligase B).	2.07578e-54
NZ_LN831776.1|WP_039788072.1|1698128_1698944_+|sulfate-ABC-transporter-permease-subunit-CysT	gnl|CDD|131194	TIGR02139, permease_CysT, sulfate ABC transporter, permease protein CysT. This model represents CysT, one of two homologous, tandem permeases in the sulfate ABC transporter system; the other is CysW (TIGR02140). The sulfate transporter has been described in E. coli as transporting sulfate, thiosulfate, selenate, and selenite. Sulfate transporters may also transport molybdate ion if a specific molybdate transporter is not present. [Transport and binding proteins, Anions].	1.48068e-80
NZ_LN831776.1|WP_020428303.1|1708229_1708889_+|ABC-transporter-permease	gnl|CDD|224922	COG2011, AbcD, ABC-type metal ion transport system, permease component [Inorganic ion transport and metabolism].	1.20174e-89

Protein sequences

>NZ_LN831776.1|WP_020428309.1|1702440_1703223_+|MBL-fold-metallo-hydrolase
MDTLVFLGTGDAMGVPRVYCSCETCMEARSSGDNARLRSSVLIDNGSDFWVIDCGPDWRRQMELQGRRGMHRLLVTHPHFDHIGGLPEWADSCRWMGYRGELYAPAEVIPVIQRQYPWLGGQIDMIPCDDGLELDGWQIRTWRVNHGKNGYSYAYRLEKDGYTWVYCPDSISLGPEETKHMHGADLLVLGTSFYYESAELSTRSVYDMTEAAELLDIVQPVRAVYTHMSHDVDMRKDYILPGNVTLAVTGLKLRLGHAEG
>NZ_LN831776.1|WP_039788070.1|1700821_1701889_+|sulfate-ABC-transporter-substrate-binding-protein
MRLFKRSRQLHGWLAALMLAVLALAVAGCGNGKESTAAEKPQQGDLTLVVGAYSVAKDAMGEILPLFAAAWKAKTGQTLTFQQSYEASGTQARAIAGGFEADVTLLAMEGDVDKLVKAGLVEADWKDRGVNGMVTRSVVALGTREGNPKGIHDFADLAKPGVKVLYPNPKTSGGAQWDINAIYGAGLKLSEEQEGAKDPAAAKAFLESVHANVESLDKSGRASMAAFEYGVGDVIVTYENELLARIAQGVKYEVIIPRNTILIENPAAVVNKYAEEHGTSEAAQALVDYLTTPEAQQVFAKYGFRPVDEQVYAENEGRYPVPAGLFDISYLGGWDKVRTTLYSKRGIWYQVLAGI
>NZ_LN831776.1|WP_020428311.1|1699739_1700801_+|sulfate-ABC-transporter-ATP-binding-protein
MHVEVRGLNKHFGDFHAVKDVNFGITKGHLIGLLGPSGGGKTSILRMLAGLETPDSGEIVFHGRTVNNLPPQEREIGFVFQNYALFKHMTVYENIAFGLKVKKANKHTIQNRVAELVELTGLKGFEKRYPHQLSGGQRQRVAFARALAPEPQLLLLDEPFAAIDAKIRQELRSWLRELIERVGITSIFVTHDQDEAIEVADEIMIINQGRLEQKGTPWDIYKEPKTPFVATFIGESTLIESAAELKGFHNTGGKPTKALIRPEYIEVGHLNEFKMASATEQGIVKHLHFRGSEWLVEVEVNGHKLVTYRSLEKETLTPGQEIAVLVHRAYLFNDERSWIQENGLKEDPMPVFI
>NZ_LN831776.1|WP_020428312.1|1698940_1699738_+|sulfate-ABC-transporter-permease-subunit
MRKLWIGLTYLVFFLLIAAPLGKMTIGAFSEGFDGFWNALTRPEALHALMMTGFVVVVVTLLNTLFGIMMALYLVRASWLGSRVKGLLNSIVDLPYAVSPVIGGLMIVLLLGPESALGAVFEQIGLKIVYAFPGMVIATLFVTFPLMVREIMPVLQEIGSQQEEAASTLGAYGWTTFWKVTWPSIRWAVIYGVILTVARSLGEFGAVLVVSGNIMNKTQTATTLVYQDVENFNVTAAGGIALVLAAFSAGLLLLMEWSKRRKEVH
>NZ_LN831776.1|WP_039788072.1|1698128_1698944_+|sulfate-ABC-transporter-permease-subunit-CysT
MNTLLRHKGWTWGFRTTILLYFVVLIVLPILGVYYNSFSLGFSNFAESISDPIAWKSVLLTLKLAVMATVINVLLGTMIAWVLIRYQFPGKALLNSLVDLPFALPTAVGGLMILLLLGPGSLIGGMAEALGFEIVFHQPAIVIAMVFVTFPFVIRAVQPLLEELDASEEEAAYTMGATRSRVFRQVILPSMAPGMIGGGMLAFSRALAEFGAVVLVAGNIPGRTLVSSVFIFGEVESDNPVGAAAVSVILLTLSFLILWLINLLQMRGRRA
>NZ_LN831776.1|WP_020428314.1|1697540_1697942_-|YjbQ-family-protein
MLHTMEISTSKRDELRDITREVISYVKKSGVQNGIIIVYCPHTTAGIAINENADPDVKHDVLMRLDEVYPWEHPKYRHAEGNTASHLKSITVGPSQSIIIHEGALLLGRWQGIYFCEFDGPRRRQCYLKIIEG
>NZ_LN831776.1|WP_020428315.1|1696786_1697368_+|TetR/AcrR-family-transcriptional-regulator
MARRAVEQELSRERILEAARHLFITKGYRAISMRSIGQHLGYSHGSLYYHFKEKAELFYAIVVEDFNHVATLLNQVMHTPPEPGMTRVEQLILEFIRFGLDHPYQYEIMFMIRDEELLAYCRAEQGRCFELFASIVRSHMKEEGYVSEDWQSIPLTLFLSAHGFISYYIQDKVSFEDVRQAAVMHVKVLSRSL
>NZ_LN831776.1|WP_039788078.1|1696150_1696783_+|YigZ-family-protein
MLEQYRTVRSPGSREVVIRKSRFIGHVMPVETEEEAVQFIENIKKQHWNATHNCSAYMIGERDEIQRQSDDGEPSGTAGKPILEVIRSQNVKNVAIVVTRYFGGIMLGAGGLIRAYTDGAVLALEAGEVITRVLRREVFVEIDYTWLGKVENELRGRGIQTGETLFTDKVTLLCLPRNDEGDAFMAWITDLTQGQALVTEGRRLYYSEGE
>NZ_LN831776.1|WP_020428317.1|1694667_1696023_+|glucose-6-phosphate-isomerase
MSKKINFDYTKALSFFSQHEIDYFAAPVKLAHEQLHNKSGAGSDYLGWIDLPKAYDKEEFARIQQAAKKIQSDSDVLIVIGIGGSYLGARAAIEALSHSFYNNLSKDKRKTPEVYFAGNNISSTYITHLLDLVEGKDFSVNVISKSGTTTEPAIAFRIFRAALEKKYGKEEARKRIYATTDKEKGALKKLANEEGYESFIIPDDVGGRYSVLTPVGLLPIAVAGINIEEMMQGAAAAADEFNNPDVATNQSYQYAAVRNALYRKGKTTEILVNYEPSLHFVSEWWKQLYGESEGKDFKGIYPSSVDFSTDLHSMGQFIQEGNRNIFETVIQVEKVQHEISIENDPDDLDGLNFLTGKTMDFVNKKAFQGTMLAHTDGQVPNLIVTIPDQTPYTFGYLVYFFEKACGISGYLLGVNPFDQPGVEAYKKNMFALLGKPGYEKQKAELEARLTE
>NZ_LN831776.1|WP_020428318.1|1693515_1694418_-|NAD(P)-dependent-oxidoreductase
MKQIGFIGLGTMGAPMASNLLRSGFEVTVYNRTASRSEPLRAEGARVAATPQHAAEGKDVIITMISNDDSIREVFYGTGGILAVLKPGTTVVDSSTISPGLAKEIAAAVEERGGSFLDAPVTGSKPAAIEGTLVFMVGGSAGVIDQHRDIFDSMGRLLLHMGGNGSGAVAKLAHNAMVGIHNVALAEGFSIAVKSGVPADKFLELVKNGSAGSKQAELKGQKIIDNDFSNQFSLALMLKDLKLASSLSDSAGVPSPMLGVAKSMFQAGYNHGYGDEDLSAVVKSYEEWIGQKIGGDAAKE
>NZ_LN831776.1|WP_020428308.1|1703628_1704399_-|SDR-family-oxidoreductase
MLNIDFAGKTLVVTGGLTGIGKGITDLFLKAGANVAIGDIACRPGLERIHDRLVQIQMDVTISADAARLIDAAVEAFGGVDFLVNNSGTSTMDYAVDIREEDWDKVMDINAKGVYLVSQAGARQMLRQGRGGRIINIASQAGKNGYRCMGNYVASKHAVLGFTKVMALELAQAQILVNAVCPGIVETDMKRRERVEGAALRGMQPEDILAEDRSQVPLGRTAEPEDVANVVLFLASPLSSYMTGQAINVTGGMTMN
>NZ_LN831776.1|WP_020428307.1|1704420_1704876_-|S-ribosylhomocysteine-lyase
MAKVESFQLDHTKVKAPYVRVAGTEKNEKGSTVQKYDLRLLQPNADALPTAAVHTLEHLLATYLRDELEGIIDISPMGCRTGFYLIIWDEHEPADVAAALTKVLHKVLETEHVPAVSALECGNYKDHSLFSAKEYARLVLEAGISDDPFRS
>NZ_LN831776.1|WP_020428306.1|1705060_1705912_+|methionine-binding-protein
MKKKWIHSTLLVVAVALFTAGCGNDKEASGAGSDSSAQEKKTLKISFNPGPYSDQFKNGVAPYLEKKGYTITYKEFTDGIQPNVAVANGEIDANVFQHSLYLQSINEREKIDLVGVVQVPTPPMGLYSKKHNSLDEVKDGDQVNLPNEPVNMLRALNVLKDVGWITLKDNIDPLQTSLADVTSNPHNLKFIATEPAQGPRALEDVDYAAIQGNFAVSNNIKLTTALQLEKMTDPFTNIVAVDSKNKDAQFVKDIIEGYHSDEFQKYIKSNPDYEGYKLPAYFK
>NZ_LN831776.1|WP_020428305.1|1706002_1707217_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MDFIPSRIVTELPGNYFNAMKAKIALYRSRGIDVIDLASGNPDQPTPEHIVAALKEAVDKPENQGYPPFYGKSATLEAIAAFYQREYGVGLDPETEVAVFSGSGIGVVGIPQSLLNPGDLLLTVDPAYPAYHAAAALAGARVHTIPAYEAEGFLPDYGTVPEELARQVKLLMLNYPNNPTGAVATAEFFERTLAFAARYGFPVLNDFAYGAFGFDGHKPVSLLQQPGGKEYGIETYTASKTFNMAGWRFGFAVGNASIIAALKHYHTQAYSTVFGAVQDAAAAALLGPQEGVAELGRLYERRRDVLVAGLRELGWEIKAPQGTFFAWFRVPEGYTAASFAACLLDEAQVAVAEGGGFGVQGREYVRVSLVNSEDKLNEAVDRIAAAGIFKRIKLSAGQEAVRYD
>NZ_LN831776.1|WP_046501698.1|1707209_1708229_+|methionine-ABC-transporter-ATP-binding-protein
MIEIKNVYKTFERKGQSIEALRGVSLSIARGDIYGVIGYSGAGKSTLIRLVNALERPTAGEVLVEGQDLAGYNPAELRQAKKNIGMIFQHFNLLESKTVFDNIAIPLVLLKRSKQEIRERVTELLKFTGLGDKANSYPKELSGGQKQRVGIARALASNPSILLCDEATSALDPQTTKSILELLQKINEEYNITIMIITHEMAVIQQICNKVAVMERGEIIEQGNVLDVFGSPHHPTTQSFVQTVIHNSVPQSVLHTLKAENGRRLFKLKFVGGAASEPIINSLIRRYEVDVNILFANMTEIQNTTLGNMILQMHGDHAVIDRAADFITSQGVEITEVEA
>NZ_LN831776.1|WP_020428303.1|1708229_1708889_+|ABC-transporter-permease
MFDSVITSEQLFQALRETVVMVGVSLFFGALLGIPVGIILVITRPGGVLENRFVFAVLNPVINIIRSLPFIILLVAIIPFTRLLVHTSIGTSAAIVPLVVYVAPYIARLVENSLLEVSPGIMEAAEAMGATTFQVIWHFLLPEAFGSLILTMTTATIGLIGATAMAGTVGGGGIGDLAISYGYQRFDTFVMIVTVAILIIFVQGIQSAGNRLARKARRD
>NZ_LN831776.1|WP_039788062.1|1708910_1710038_+|iron-containing-alcohol-dehydrogenase-family-protein
MPVEPQIIVRAAPQEFICRPGSWGSLEQHLQRRGIRRVLVVRGNRSWTAAAPYWPELKETEVHYHVYSGECSYRERDAIAGYASEHQLEAVIAVGGGKITDLVKSAAATLNLPAIILPTLAATCAAWSSLSVMYDERGAFIRFEVFPRSNALVLLDPVVIAASPPELLAAGIGDTLAKWYEADVIIRHLEAPPVEVELAWDAARKCRENLLRYSSAALAAVRSGELNEALTRTAETIIMVAGLVGGFGEDYGRTAGAHSVHDALTAIPETHGLLHGSKVAYGVLVQLALEGNWPEIDGLLPFYEELGLPSSLRAMGLGHLTREELLKLGERAAVPEASIHMMPGVITAEAVADAVAELEEYITAGQNQTKGEGIL
>NZ_LN831776.1|WP_020428301.1|1710034_1710754_+|5'-methylthioadenosine/adenosylhomocysteine-nucleosidase
MSIAVIGAMEEEVAPLLPKLRDVRSLKAGGGKLYAGVLDGQEVVLLQSGIGKVNAAVTTTLLLERFHCELIINTGAAGGLAADLKVGDVVIAEELVYSDVDATAFSYAFGQVPQMPQRYPVAAGLLAQARKLVRRGVRQEQIVTGLITTADSFISDPERAVSIVSRFPEAKATDMEGAAIAQTAYQFGVPFLAVRAISDIAGSDAAGLFKSHLELAAANSAEVVLEILSQYKPPESFEI
>NZ_LN831776.1|WP_020428300.1|1711002_1711587_+|GNAT-family-N-acetyltransferase
MKSDPFIPVLFDFPEFFETERLLVRAPQWGDGRAVNEAIRESLEELKPWMPFAQSMPALEESEIYVRDSRLKFLNRTVLNMLIFHKTEGTFLGCTGLHHIDWETRCFEAGYWLRTTCTGKGYITEAVNGITRFAIQELAANRIEIRCSGLNTRSAAVAERAGFLLDGTLRLNTLGLDGEMHDSKVYAKVRGAEF
>NZ_LN831776.1|WP_052741422.1|1711655_1712201_+|DUF5071-domain-containing-protein
MNHNVLPKNKQNFKSVEALARLERSMIIPLLPELLEWLQEMNWPIAAEIVDLLSKYKSETIPHIKTVFSQSDSIWIYNILAYLINKWDTDLVSILSSSLGELAHTIDIYEDTDLLSIEILWKVMFSELENERLHILNTDIGQIVNYCERNNKLLMQKDQYQNSLRRYEEIEATIRSISAFT

Crispr_ID: NZ_LN831776_26

• CRISPR_ID: NZ_LN831776_26
• CRISPR_location: 1861317-1861391
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: RT,DEDDh

Consensus repeat of NZ_LN831776_26

Consensus_repeat	Method
AATTAGTGTCCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_26

>26.1|1861340|29|NZ_LN831776|CRISPRCasFinder
CATCTGCCCGAGGATAGGGTACTTCGGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_26

CRISPR arrays

The CRISPR arrays of NZ_LN831776_26

>merge|NZ_LN831776|26|1861317-1861391|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTTCATCTGCCCGAGGATAGGGTACTTCGGCAAATTAGTGTCCCTTATTCCACTT

>NZ_LN831776|26|28|1861317-1861391|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTT	CATCTGCCCGAGGATAGGGTACTTCGGCA
AATTAGTGTCCCTTATTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020425999.1|1852581_1853874_+|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	gnl|CDD|275209
NZ_LN831776.1|WP_020431243.1|1850167_1851973_+|adenine-deaminase	unknown	unknown	gnl|CDD|223933
NZ_LN831776.1|WP_020426001.1|1867503_1868478_+|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|380514
NZ_LN831776.1|WP_039785360.1|1863052_1863937_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_039835926.1|1854230_1854683_+|IDEAL-domain-containing-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046501819.1|1864944_1865907_+|carbohydrate-kinase	unknown	unknown	gnl|CDD|238572
NZ_LN831776.1|WP_020425991.1|1859697_1860654_+|HD-domain-containing-protein	unknown	unknown	gnl|CDD|237394
NZ_LN831776.1|WP_020425993.1|1855548_1856565_-|ferrochelatase	unknown	unknown	gnl|CDD|234585
NZ_LN831776.1|WP_020425992.1|1857062_1859459_+|FMN-binding-protein	unknown	unknown	gnl|CDD|223021
NZ_LN831776.1|WP_020426002.1|1865920_1867387_+|sucrose-phosphorylase	unknown	unknown	gnl|CDD|200492
NZ_LN831776.1|WP_020426006.1|1861662_1862985_+|carbohydrate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|224567
NZ_LN831776.1|WP_020430942.1|1871757_1872651_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223656
NZ_LN831776.1|WP_144412091.1|1854906_1855332_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046501814.1|1847199_1848483_+|Zn-dependent-hydrolase	unknown	unknown	gnl|CDD|236456
NZ_LN831776.1|WP_020431238.1|1845808_1847203_+|allantoinase	unknown	unknown	gnl|CDD|235732
NZ_LN831776.1|WP_020426004.1|1863936_1864764_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_082118076.1|1869674_1870940_+|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_LN831776.1|WP_020426000.1|1868621_1869311_-|3'-5'-exonuclease	DEDDh	cd06127_DEDDh_CAS-I	gnl|CDD|99834
NZ_LN831776.1|WP_020430944.1|1870891_1871476_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831776.1|WP_020431241.1|1848505_1849729_+|alanine--glyoxylate-aminotransferase-family-protein	unknown	unknown	gnl|CDD|223153

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831776.1|WP_020425999.1|1852581_1853874_+|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	9.8e-52	170.3	0.0
NZ_LN831776.1|WP_020426000.1|1868621_1869311_-|3'-5'-exonuclease	DEDDh	cd06127_DEDDh_CAS-I	6.6e-32	105.6	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020425999.1|1852581_1853874_+|group-II-intron-reverse-transcriptase/maturase	gnl|CDD|275209	TIGR04416, hypothetical_protein, group II intron reverse transcriptase/maturase. Members of this protein family are multifunctional proteins encoded in most examples of bacterial group II introns. These group II introns are mobile selfish genetic elements, often with multiple highly identical copies per genome. Member proteins have an N-terminal reverse transcriptase (RNA-directed DNA polymerase) domain (pfam00078) followed by an RNA-binding maturase domain (pfam08388). Some members of this family may have an additional C-terminal DNA endonuclease domain that this model does not cover. A region of the group II intron ribozyme structure should be detectable nearby on the genome by Rfam model RF00029. [Mobile and extrachromosomal element functions, Other].	0
NZ_LN831776.1|WP_020426001.1|1867503_1868478_+|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|380514	cd06291, PBP1_Qymf-like, ligand binding domain of the lacI-like transcription regulator from a novel metal-reducing bacterium Alkaliphilus Metalliredigens (strain Qymf) and its close homologs. This group includes the ligand binding domain of the lacI-like transcription regulator from a novel metal-reducing bacterium Alkaliphilus metalliredigens (strain Qymf) and its close homologs. Qymf is a strict anaerobe that could be grown in the presence of borax and its cells are straight rods that produce endospores. This group is a member of the LacI-GalR family repressors that are composed of two functional domains: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal ligand-binding domain, which is homologous to the sugar-binding domain of ABC-type transport systems that contain the type 1 periplasmic binding protein-like fold. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcription repressor undergoes a conformational change upon ligand binding which in turn changes the DNA binding affinity of the repressor.	5.19734e-116
NZ_LN831776.1|WP_039785360.1|1863052_1863937_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	2.05887e-72
NZ_LN831776.1|WP_020431241.1|1848505_1849729_+|alanine--glyoxylate-aminotransferase-family-protein	gnl|CDD|223153	COG0075, COG0075, Serine-pyruvate aminotransferase/archaeal aspartate aminotransferase [Amino acid transport and metabolism].	8.40537e-156
NZ_LN831776.1|WP_046501819.1|1864944_1865907_+|carbohydrate-kinase	gnl|CDD|238572	cd01167, bac_FRK, Fructokinases (FRKs) mainly from bacteria and plants are enzymes with high specificity for fructose, as are all FRKs, but they catalyzes the conversion of fructose to fructose-6-phosphate, which is an entry point into glycolysis via conversion into glucose-6-phosphate. This is in contrast to FRKs [or ketohexokinases (KHKs)] from mammalia and halophilic archaebacteria, which phosphorylate fructose to fructose-1-phosphate.	7.25565e-67
NZ_LN831776.1|WP_020425991.1|1859697_1860654_+|HD-domain-containing-protein	gnl|CDD|237394	PRK13480, PRK13480, 3'-5' exoribonuclease YhaM; Provisional.	1.04848e-90
NZ_LN831776.1|WP_020425993.1|1855548_1856565_-|ferrochelatase	gnl|CDD|234585	PRK00035, hemH, ferrochelatase; Reviewed.	4.02438e-123
NZ_LN831776.1|WP_020425992.1|1857062_1859459_+|FMN-binding-protein	gnl|CDD|223021	PHA03247, PHA03247, large tegument protein UL36; Provisional.	1.1768e-12
NZ_LN831776.1|WP_020426002.1|1865920_1867387_+|sucrose-phosphorylase	gnl|CDD|200492	cd11355, AmyAc_Sucrose_phosphorylase, Alpha amylase catalytic domain found in sucrose phosphorylase (also called sucrose glucosyltransferase, disaccharide glucosyltransferase, and sucrose-phosphate alpha-D glucosyltransferase). Sucrose phosphorylase is a bacterial enzyme that catalyzes the phosphorolysis of sucrose to yield glucose-1-phosphate and fructose. These enzymes do not have the conserved calcium ion present in other alpha amylase family enzymes. The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues (Asp, Glu and Asp) performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase.	0
NZ_LN831776.1|WP_020426006.1|1861662_1862985_+|carbohydrate-ABC-transporter-substrate-binding-protein	gnl|CDD|224567	COG1653, UgpB, ABC-type sugar transport system, periplasmic component [Carbohydrate transport and metabolism].	1.92952e-29
NZ_LN831776.1|WP_020430942.1|1871757_1872651_+|LysR-family-transcriptional-regulator	gnl|CDD|223656	COG0583, LysR, Transcriptional regulator [Transcription].	9.57631e-49
NZ_LN831776.1|WP_020431243.1|1850167_1851973_+|adenine-deaminase	gnl|CDD|223933	COG1001, AdeC, Adenine deaminase [Nucleotide transport and metabolism].	0
NZ_LN831776.1|WP_046501814.1|1847199_1848483_+|Zn-dependent-hydrolase	gnl|CDD|236456	PRK09290, PRK09290, allantoate amidohydrolase; Reviewed.	5.85191e-170
NZ_LN831776.1|WP_020431238.1|1845808_1847203_+|allantoinase	gnl|CDD|235732	PRK06189, PRK06189, allantoinase; Provisional.	0
NZ_LN831776.1|WP_020426004.1|1863936_1864764_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.94588e-67
NZ_LN831776.1|WP_082118076.1|1869674_1870940_+|MFS-transporter	gnl|CDD|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	7.1511e-58
NZ_LN831776.1|WP_020426000.1|1868621_1869311_-|3'-5'-exonuclease	gnl|CDD|99834	cd06130, DNA_pol_III_epsilon_like, an uncharacterized bacterial subgroup of the DEDDh 3'-5' exonuclease domain family with similarity to the epsilon subunit of DNA polymerase III. This subfamily is composed of uncharacterized bacterial proteins with similarity to the epsilon subunit of DNA polymerase III (Pol III), a multisubunit polymerase which is the main DNA replicating enzyme in bacteria, functioning as the chromosomal replicase. The Pol III holoenzyme is a complex of ten different subunits, three of which (alpha, epsilon, and theta) compose the catalytic core. The Pol III epsilon subunit, encoded by the dnaQ gene, is a DEDDh-type 3'-5' exonuclease which is responsible for the proofreading activity of the polymerase, increasing the fidelity of DNA synthesis. It contains three conserved sequence motifs termed ExoI, ExoII and ExoIII, with a specific Hx(4)D conserved pattern at ExoIII. These motifs are clustered around the active site and contain four conserved acidic residues that serve as ligands for the two metal ions required for catalysis. The epsilon subunit of Pol III also functions as a stabilizer of the holoenzyme complex.	5.9656e-86
NZ_LN831776.1|WP_020430944.1|1870891_1871476_-|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	2.22823e-11

Protein sequences

>NZ_LN831776.1|WP_020425991.1|1859697_1860654_+|HD-domain-containing-protein
MTLIKQLSPQDEFVGFYLLRELAIKQTNGTPPKDYFDIVLGDSSGQISAKYWDASTTDKETFFPMALVKIRGIAHTYREKLQVKITKIRLANDGDNVSLTDFIRSAPIRPVDLIHTIKGVMASITDPEIATIVSFCVGKVEKKLMHYPAAKTHHHAYFAGLAYHMVRMLEIGEFLCKQRPFLNPDLMKAGIILHDIAKPEEMISQFGIVSDYSVQGKLIGHISMASNWITEAAIRSGIDLESEKVLGLQHLVLSHHNLGEWGSPVQPQTAEAVALHHIDALDAKLQMVEDALDTTPETEEWTPFIRGLENKAVYRMKI
>NZ_LN831776.1|WP_020425992.1|1857062_1859459_+|FMN-binding-protein
MKKLISLTVSAALLLAPLAYTINAPALNLKVDAVSAASEEAPAATAKPAEPKPAAKPTAKPTAKPTVKPKPTVKPTPKPTAKPTPKTTAKPAATAKATAKPAATAKPTATANPSATAKPVATAKPGSTVKPTATAAPAVTAEPTATAAPAVTVEPAATIAPAAAAKPVTVKQNVYQDGVYTAYGNAYSKGTEGAKVTIKDGKITDIELLRTSPKLIDRNARENYSGVWVAYKLMKDRLLGQTRDSAAAVDAVSGATRSSNGWKLSVDRAFERALKVKPADAVYFAGDHMGVDPEGKYAVFASYDANKLTAVKLYPLNAAGDFVDEKTYTAEQTAAIAAITPVLLANGSSAQPVAGFEAESKAAIKAFWDAEQNASINNTSAYIDGFYSSYGTARNVGVERADVVIRNGRLVDVKLYRLGTNLIDRGATAYAEVVKANAPMTAKLLANGSYIANYNEKVDGISGATESSHGWNQAVERAFGKALKAPAAGRYFDGKFAGVDNASRIFILVDVAADQVTSIKLSLFGTDGKLIADDKLTAEQKTLVEQLTAGLLDKGVQIADVTGQEALTAAARAALTDALTNASKEQGAYKDGTFTAYGDAYDKGTNKADVTLRNGKIVNVALSRVGMNMVDLGKNAYAEVQKALPQLTANFFAAGTREGVQQVDAVSGATSSSNALKAAVDRAYGKAEVVEAGKAAYFNGTFIGVSTDKTVNVMVTVKYNVPVTMVVYYLDAAGKVKAYDQLTEAEKAVKAEIENTSSGNGLHKYGYRAAAFGSNDAEKEVSAKAVEAIKAALEAAGK
>NZ_LN831776.1|WP_020425993.1|1855548_1856565_-|ferrochelatase
MLPPAPIGVILAQIGTPEAPTAKAVRPYLRRFLSDRRIIDYPPFFWQPLLRGIILRIRPRRSALLYSQIWQKDGSPLLLHSLDQRAGLQRLLGNRYLVELGLAYSAPSMEQAMGKLEAAGATRVVVVPLFPQYSSTTTASVYDAASFAALGRRSASGPVTKRFVPALRFMEAYYNEPGYIWAMKEHLMQQISRLSTPPDYYVLSFHGIPRRYADTGDPYPLQCLETARLLAEAMGWETGCWQAAFQSRFGREEWIGPSTSEVLKELAGRGIRRPMIFSPGLTTDCLETLHELAIEGREHFAAGGGQPENLFAAPCLNDNEEWLSFLAELVERNALGWI
>NZ_LN831776.1|WP_144412091.1|1854906_1855332_+|hypothetical-protein
MSEMRGRNTFDSARSGQLSEMRGRNTFDLARSGQLSEMRGKSTFDLARSGQLSEIRGINTFDLARSGRLSEMRGRNTFDLVRSGQLSEMRGKSTFDLARSEHRAGSLLSGVVIQGIPLPDQAPNPGAQLTLRHLKRWNRPD
>NZ_LN831776.1|WP_039835926.1|1854230_1854683_+|IDEAL-domain-containing-protein
MMRLDTQDIVNITRKQIAAIFKIEPVELRFVNDFQGEQYLLTNDKLHLSNQHYWAKVMDCVFDSHTRPVLMCEVLYFLRSEFLESDIKLRFSYDFAEGANGAATAWAEVSFNDSPELQPEEIAELIDFALSLQDKQWFEELTAKYKQLTV
>NZ_LN831776.1|WP_020425999.1|1852581_1853874_+|group-II-intron-reverse-transcriptase/maturase
MNAKGLTTPKEKVQELQEKLGHAAKENKKRKFHALYDKVYRPDVLCEAWKRVKANKGAAGVDAVTLADIEERGETNFLKTCERELKEGSYHPQPVRRHYIPKKDGKPRPLGIPTVRDRVIQMATKLVIEPIFEADFEEVSFGFRPKRSAKGALERIRKACNRKGNWVVDVDIQGYFDNINQEKLMKLVQMRINDRRILKLIRKWLQAGVMEEGNVRRSDLGTPQGGVISPLLANIYLNYFDRLWEKHGSGLGELTRYADDFVVVCKTKKDAEHAYELISRIMERLELTLHPTKTRIVGLWTGDEGFDFLGMHHRKTKAETSQGKVYYTTQQWLTKKAEERIRGVVKERLAPPSMRSRTLAEQVEWLNPKIQGWRNYYYTNYSQKRLAKLDWYILQRLTRWYAKKRQRGRWMRSRSEVKYLTIQYGLKTLL
>NZ_LN831776.1|WP_020431243.1|1850167_1851973_+|adenine-deaminase
MSFTRKPLADCVPELVATARGDLPATLVITGGKLVNVCSGEILEGMSVAVQGGRIAYVGKDVSHMIGEGTRVIEAAGRYIAPGMLDGHCHIESTQLTVTEFARAVLPLGTTGGFFDAHEIANVFGLKGIRLMLEEMRGTPLAAYMQVASCVPSAGPEFETTGASIGPEEVAEAYTWGEDVIALGEVMNFPGVVYGDSKMLGEIQATLRAGRVVDGHFTWPADDWRLPVYAAAGVTGDHECVTAEDVIERVRLGMYAQMRRGSAWHDVAKTITAHTEHGLDPRRMLLVTDDRSSESLRDEGHMDFVVRHAISQGVKPVTAFQMATINTAERFGVARDIGSITPGSCADIILLDGNLADVHVVMTIAAGVVVAENGIMTASLAPYAYPGEVLASVHLPQLPVAEDFVIRAPIESGSVLTRVIRVIENHVETEELILDLPVSEGRLQVGNGLCKIAVLERHKGTGNKSVGVAAGIGFHEPAAIAMTVAHDSHNVLVIGNDDGLMAQAAGAVAEAQGGVAVITGTGTTLFPLAIAGLMSVEPFEMAAAKSAAVSKALYDSGCTLNYAFMTLSLLALAVIPTLRISDKGLVRISPEEGIKLVSLFV
>NZ_LN831776.1|WP_020431241.1|1848505_1849729_+|alanine--glyoxylate-aminotransferase-family-protein
MKRYEDLSPALRCIMTPGPVEVDPRVLRAMSFPVLGQFDPEFTDIMNETMGMLRELFATGNQWAFPVDGTSRSGIEAVMVSLIAPGDRVLIPIFGRFGHLLHEIAERCGAEVFTIETAWGSVFAPEEVIAAIRSFNPDVVAMVHGETSTGRVQPLAEIGRACRGHDALLIVDAVATIGGVPVETDAWMLDAVIGGTQKCLSVPSGMAPVTYNERAEAKLMKRKQVERGLRTGGAARSELPVVGSNYFDLGMLQDYWSEQRLNHHTEMTSMLYALREGLRLVLEEGLEKRYARHVLHERALTAGLAAMGLKLYGDPESKLTVVTCVLIPEGVDGESVRAMLLERFGIEIASSFGPLKGLIWRIGTMGFSCRENNVLRLLGALEAVLLRHGYAVPCGLGVQAALDVYEA
>NZ_LN831776.1|WP_046501814.1|1847199_1848483_+|Zn-dependent-hydrolase
MMKPVIQVPAAAMLELLQELTAFSAPGPGVTRLLYTPEWSGAQHFLQEKMAGLGLEVHTDSVGNVFGRLNGSEPSSSVILTGSHIDTVVNGGKYDGAYGVAAAVTALHYLAETFGPPLRTLEVVAFCEEEGSRFPLAFWGSGNVTGLYNGWVADSIADPEGVTLMEAMNACGLGTGGSRIDSEESSGRGADSARREDIGMYVELHIEQGILLEQSAEQIGVVQAIAGQRRFTVKVTGTANHAGTTPMGLRRDALAGTAEMLCALERSAAKAGAPLVATAGRLEVIPGTPNVIPGEVQFTLDIRHSEAARLESFCAALAAAFGEIAARRGLALELVPTLATSPAPMNQALCGALEQICLEQGRSFRRMVSGAGHDAQLFAPKCPAAMIFVPSRAGISHSPEEYSSPEELAAGLNVLTALLYKLAYEAS
>NZ_LN831776.1|WP_020431238.1|1845808_1847203_+|allantoinase
MEEAYELIIRNGDVVLPGEVRKLDVGVQDGKIAALGQGLQAAAATTVIDAEGQYVLPGMIDMHVHFNEPAFGHWEGFRSGSAALAAGGCTCYADMPLNGNPPTVNRAALQLKAEAASGNSAVDYMLWGGLVPGNLAELEGLAAAGVTGFKAFISNPGGEGEGRFREVDDGTLFLGMQKIAALGGILALHAESEDITAMLSAGAVRSGRTGARDFAASRPAMAELEAVSRALLYSERTGCRLHFVHISTAAAVEMIHAAKRRGLDVTAETCPHYLVLNEDSMEQLGPVAKCAPPLRSTQEQQELWKVLAEGRIDLIASDHSPCPPELKFDPGLTFFEAWGGISGAQSSLELMFHEGVHMRGLPVTQVSALLSGQPARRFGLDHRKGSIAPGLDADLVLLNPKAGYTLAAGDLLYRHKHSPYIGMTLSCKVTTTVCRGNVVYTAEQGVVSADKGEWLQIYNAQQAP
>NZ_LN831776.1|WP_020426006.1|1861662_1862985_+|carbohydrate-ABC-transporter-substrate-binding-protein
MKGFKKVSLTALTLILSASLSACGSSDSKSTTSSDKSGTDKSVKITLLNSKGEIQTQLEDAAKSFHEAYPDITLEVQQVPSGTSPFERASTLYASGNQPTMIMLDTGDVAKFKDHILDLSDAKWNGDAIDSALDLTTFDGKNYAFPLAVEGYGLIYNKAVLDKAVGGNFDPASINTTSSLEELFKKIEASGKKALTISPMDWSLGAHYLSLAYGGQSKDSKEVAGFISSLRAGTVDLSSNKVFNGLMDTFDVMMKYNMDQASPLSPTYEKGPEVLGKGEVGIWFMGNWAWPQISGFDTADKQYGFLPVPVSNNPDDYGNTQISAAVSKRIVVDKEKTTPEQQAAAKKFFDWIVYEQAGQDFLVNKANIVPAFKNITMETPDPLGKSIQTYLAAGKVEPSLSDLPADHWTKVGASMQKYLSKAGDRATLAKEIQDYWKTVK
>NZ_LN831776.1|WP_039785360.1|1863052_1863937_+|sugar-ABC-transporter-permease
MTGEKGFWNRLRLRLLFTGPTLFAFLTVMIIPFVYGIYLTFTSWDGISVGHTLVGFRNYGSVFADSEFWSSFGLTLKYVLFTVVLTNVLAFMLAYALTKRVRGQNVFRAGFFMPNLVGGIVLGFIWQFIFNNVLVYLGQKASIGIFSASWLAEPGKAFWTLVIVTVWQYAGYMMVIYVAGLTGVPADIQEAASIDGANSWQKLTRMTIPMMVPSFIVCLFLSLQRGFMVYDLNLTLTKGGPFGSTQLVSMHVYQKAFLSRDYGVGQAEAFVLFLLVAVITLLQVYFSKKMEVEA
>NZ_LN831776.1|WP_020426004.1|1863936_1864764_+|carbohydrate-ABC-transporter-permease
MRVQRQLGSAAKFVVLAILLVLFLVPFLLLMLNSLKENAMITSNPLALPTSFKFANYSYAFKQMNYVDAFTNTIIITALSVILIGICGAMTAHYFVRNPSRLNQNTFLFMVASMIIPFQAIMIPLVKIYGSLDMLNSKTSLIFMYLGFGSSLAVFIYHGFIKSIPKELEEAAMIDGCSRIRMFFQIVFPVLVPTTVTIGILNVLWIWNDFLLPSLVLVEAGQRTLPLSTYSFYGTYTVDYGPLMASLMLTILPVVIVYLFAQKYIIQGVMQGSVK
>NZ_LN831776.1|WP_046501819.1|1864944_1865907_+|carbohydrate-kinase
MVFKLDERIKLPADREYDVLSAGEMLVDFISEEDQNTAGQGTYHPFFGGAPSNIAMNISRLGIRPIVASAVGNDRLGFFLVESLKKAGIDTKCVQIVEDSTSLVLITKSTSTPVPIFYRAADYQLAYTPELEQAVLKAGFVHFSCWPISMEPSRQTINRVIEAAKRRGIPVCFDPNYHPQVWRKGEDGTAYVKKIISQADIVKPSEDDAERLFGRDTPENQVQKYIALGAGLVIMTLGKDGAIVSNGQETARFETLAHEVVDTTGAGDAFWSGFYTALVRGATVREALRSGFAVSAFKLKYTGAVVPLPDLNIIQAEYGC
>NZ_LN831776.1|WP_020426002.1|1865920_1867387_+|sucrose-phosphorylase
MVKNQVQLITYPDSLGGDLKSLHHALDVYFPDVFKGGVHILPPFPSSGDRGFAPLTYLEIEPAFGDWADIRAIGERHDVLVDLMVNHISRQSPYFQDVLQHGRQSRYADLFLTLDKIWADGQPVQADIDKMFLRRSKPYSTFTIQDTGEELQVWTTFGKNDPSEQIDLDIRSEKVKQLFIQFFTCFKENNIKIVRLDAVGYVIKKLGTSCFFVEPEIYGFLDWIKELADSLDIELLPEVHSHYSIQYKLAEHGCWIYDFILPYRILDTLLNKDSRGLREYLRTRPAKQFTMLDCHDGVPVKPDLDDLIDTKDAQKIVDICVERGANLSLILSDEHKAPDGFDVHQIRCSYYSVLNCDDDAYLAARAIQFFAPGIPQVYYVGLLAGENDLERVRETGEGREINRRNYTLPEIGQSLEKEVVQRLLKLIRFRNEYEAFNGDFTVEEAAADEIRLSWKKGEFRCTLYINLDTMRSEIEYTDGEGVLAQLEV
>NZ_LN831776.1|WP_020426001.1|1867503_1868478_+|LacI-family-DNA-binding-transcriptional-regulator
MATINDVAEQAGVSVTTVSRVLNNRGYISEKTRQKVYQVMDELNYQPNELARSLLRKHSNVLGLIIPSVAHPFFGELANAIESVAYQHGFKLLLCNSQLDSAKEREYVDMMRRNRVDGMILGSHTLEIGDYTHLNYPLVTIDRRIGDIPFVASDNENGGALAARLLIAKGCRKIGHLSGNMKLDMLSNLRTTGFEREARQGGVKFVTYQTELDVFDEQIYNEIIRKMFTEHPDIDGVFATSDLMALFVMKWCRTFGKEVPRDVRIIGYDDIDAASWYMPGLSTIKQPIKDMARRAVELLLEQMDDKTVERETVLPVELVEREST
>NZ_LN831776.1|WP_020426000.1|1868621_1869311_-|3'-5'-exonuclease
MNFTAIDFETANSSRSSACALGLVQVREGVVSAEHVWLIDPQQRFDGMNIAIHGITPSMVEGKPTFDELWPTLEPLLQGEVVIAHNAAFDMSVLRYCLDRTAYSYPEFQYMCTYLLGKKMLQELPSHKLNVVSQHFGISLKHHDALDDARAAAAILLKLMEREQHTDPLLLAGSQGYKAGTMYAGGYTPFKSPPKKPAKKAAAKKSTPPPSSRPAKSTSGSSSALGNFF
>NZ_LN831776.1|WP_082118076.1|1869674_1870940_+|MFS-transporter
MEEGNEFGILIQEDFMIPNKQISKSISKPTSKSISKNTVCMFLTYFFSSLGAYIFDIGIIVELYKISGSTIAVGGFFIVQFIPSLILTPIAGALIDRLNQKYILLFVNILRGAAVALLLVHLSIETIYIVAVILGICDETSSSTISSIIPQTTPSEDISKINSVLSTTDSVNMIFGPAIAGLLITLAGINGSISAVIFTFILAGLMILFIEYKYEKAVNEKSKHFITEIKEGLEIVTKSKLVKKIILIWGFLLIGVGATGSLIVIMLSDYMHLPTESYGWIMTAEGIGLVIGSVVIIRKKKPYHHYDLIVAGMILLGVSLMITSFADNLFVVLGAYLFVGLGAASAPNGIRTTLQTELPVEILGRVFTTTRFIINTLRTLSIAIASILSKFMSLRMIFFIAACFILYGAFSSRGLKRLERV
>NZ_LN831776.1|WP_020430944.1|1870891_1871476_-|GNAT-family-N-acetyltransferase
MSNSKEILIRNAADSDRDAIAKVLLEAYGQYAAELPEPFWAEYRRSILDSVHGTAPYARIVAEIDNRIVGSVLLFLSSEEAYGRPELGIRSPIIRLLAVSPSVRGRGIAVLLIREAARRSIGLGAATLNLHTSDMMASAVKLYERLGFQRAYETDIMNGDTLVKGYCLDLGAFSLPHALQTLSRRFKPLDEKAP
>NZ_LN831776.1|WP_020430942.1|1871757_1872651_+|LysR-family-transcriptional-regulator
MNIENIEAFVYINHYGSFNKAADVLYISQPTVTARIHSLERELDCRVFDRVGKQINLTDKGRQFLPYAQQILQVYQSGKHQVQSKGLVPDELRIGSTISVSNYLMPQLLVHLKGAYPNLNIKLTTAPTEVLIDKLKAKDIDLAFIRKVVNPAIQAYPFCEDPISLYVYEGHPLAQARRASIQDIRRETLVFFECGSLDWLRLHRVFESMEQPPDIVYQVDNLETAKKLVLRKAGIAFLPALSVQEEVAAGTLTRVEIAETEGISLRTSLISLNGEYAGFIQTLLELGTGNQLNRLIV

Crispr_ID: NZ_LN831776_27

• CRISPR_ID: NZ_LN831776_27
• CRISPR_location: 2153697-2153771
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_27

Consensus_repeat	Method
AATTAGTGTCCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_27

>27.1|2153720|29|NZ_LN831776|CRISPRCasFinder
CATCTGCCCGAGGGTAGGGTACTTCGGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_27

CRISPR arrays

The CRISPR arrays of NZ_LN831776_27

>merge|NZ_LN831776|27|2153697-2153771|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTTCATCTGCCCGAGGGTAGGGTACTTCGGCAAATTAATGTCCCTTTTTCCACTT

>NZ_LN831776|27|29|2153697-2153771|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTT	CATCTGCCCGAGGGTAGGGTACTTCGGCA
AATTAATGTCCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020428886.1|2155850_2156729_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_046501924.1|2154450_2155776_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_LN831776.1|WP_020434149.1|2152050_2153163_+|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_020434152.1|2146670_2148965_-|alpha-galactosidase	unknown	unknown	gnl|CDD|225882
NZ_LN831776.1|WP_052741430.1|2162889_2163993_+|hypothetical-protein	unknown	unknown	gnl|CDD|99882
NZ_LN831776.1|WP_020427649.1|2164441_2165620_+|glycosyltransferase-family-4-protein	unknown	unknown	gnl|CDD|340831
NZ_LN831776.1|WP_020434153.1|2144801_2146154_-|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl|CDD|199834
NZ_LN831776.1|WP_020434155.1|2142586_2143720_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020428888.1|2156752_2157595_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_020427653.1|2159475_2160387_-|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_LN831776.1|WP_046501919.1|2149056_2150046_-|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|380486
NZ_LN831776.1|WP_020434154.1|2143812_2144685_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427652.1|2161747_2162887_+|DUF1611-domain-containing-protein	unknown	unknown	gnl|CDD|225902
NZ_LN831776.1|WP_046501913.1|2136990_2138019_+|hypothetical-protein	unknown	unknown	gnl|CDD|379597
NZ_LN831776.1|WP_046501914.1|2138111_2141702_-|hypothetical-protein	unknown	unknown	gnl|CDD|349463
NZ_LN831776.1|WP_046501931.1|2160585_2161728_+|DUF1611-domain-containing-protein	unknown	unknown	gnl|CDD|225902
NZ_LN831776.1|WP_020427650.1|2163985_2164420_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020434150.1|2150234_2152073_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_046501928.1|2158161_2159427_-|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_LN831776.1|WP_020434156.1|2141987_2142605_+|RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|274357

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020428886.1|2155850_2156729_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	6.9019e-74
NZ_LN831776.1|WP_046501924.1|2154450_2155776_+|extracellular-solute-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	6.19049e-31
NZ_LN831776.1|WP_020434149.1|2152050_2153163_+|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	4.41137e-54
NZ_LN831776.1|WP_020434152.1|2146670_2148965_-|alpha-galactosidase	gnl|CDD|225882	COG3345, GalA, Alpha-galactosidase [Carbohydrate transport and metabolism].	0
NZ_LN831776.1|WP_052741430.1|2162889_2163993_+|hypothetical-protein	gnl|CDD|99882	cd05807, CBM20_CGTase, CGTase, C-terminal CBM20 (carbohydrate-binding module, family 20) domain. CGTase, also known as cyclodextrin glycosyltransferase and cyclodextrin glucanotransferase, catalyzes the formation of various cyclodextrins (alpha-1,4-glucans) from starch. CGTase has, in addition to its C-terminal CBM20 domain, an N-terminal catalytic domain belonging to glycosyl hydrolase family 13 and an IPT domain of unknown function. The CBM20 domain is found in a large number of starch degrading enzymes including alpha-amylase, beta-amylase, glucoamylase, and CGTase (cyclodextrin glucanotransferase). CBM20 is also present in proteins that have a regulatory role in starch metabolism in plants (e.g. alpha-amylase) or glycogen metabolism in mammals (e.g. laforin). CBM20 folds as an antiparallel beta-barrel structure with two starch binding sites. These two sites are thought to differ functionally with site 1 acting as the initial starch recognition site and site 2 involved in the specific recognition of appropriate regions of starch.	3.00084e-33
NZ_LN831776.1|WP_020427649.1|2164441_2165620_+|glycosyltransferase-family-4-protein	gnl|CDD|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	9.60982e-90
NZ_LN831776.1|WP_020434153.1|2144801_2146154_-|PQQ-binding-like-beta-propeller-repeat-protein	gnl|CDD|199834	cd10276, BamB_YfgL, Beta-barrel assembly machinery (Bam) complex component B and related proteins. BamB (YflG) is a non-essential component of the beta-barrel assembly machinery (Bam), a multi-subunit complex that inserts proteins with beta-barrel topology into the outer membrane. BamB has been found to interact with BamA, which in turn binds and stabilizes pre-folded beta-barrel proteins; it has been suggested that BamB participates in the stabilization.	1.99631e-17
NZ_LN831776.1|WP_046501928.1|2158161_2159427_-|MFS-transporter	gnl|CDD|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	4.7907e-55
NZ_LN831776.1|WP_020428888.1|2156752_2157595_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	4.36676e-77
NZ_LN831776.1|WP_020427653.1|2159475_2160387_-|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	2.10752e-29
NZ_LN831776.1|WP_046501919.1|2149056_2150046_-|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|380486	cd01544, PBP1_GalR, ligand-binding domain of DNA transcription repressor GalR which is one of two regulatory proteins involved in galactose transport and metabolism. Ligand-binding domain of DNA transcription repressor GalR which is one of two regulatory proteins involved in galactose transport and metabolism. Transcription of the galactose regulon genes is regulated by Gal iso-repressor (GalS) and Gal repressor (GalR) in different ways, but both repressors recognize the same DNA binding site in the absence of D-galactose. GalR is a dimeric protein like GalS and is exclusively involved in the regulation of galactose permease, the low-affinity galactose transporter. GalS is involved in regulating expression of the high-affinity galactose transporter encoded by the mgl operon. GalS and GalR are members of the LacI-GalR family of transcription regulators and both contain the type 1 periplasmic binding protein-like fold. Hence, they are structurally homologous to the periplasmic sugar binding of ABC-type transport systems.	1.90118e-110
NZ_LN831776.1|WP_020427652.1|2161747_2162887_+|DUF1611-domain-containing-protein	gnl|CDD|225902	COG3367, COG3367, Uncharacterized conserved protein [Function unknown].	1.80276e-14
NZ_LN831776.1|WP_046501913.1|2136990_2138019_+|hypothetical-protein	gnl|CDD|379597	pfam14399, BtrH_N, Butirosin biosynthesis protein H, N-terminal. BtrH_N is the N-terminus of the acyl carrier protein:aminoglycoside acyltransferase BtrH. Alternatively it can be referred to as butirosin biosynthesis protein H. BtrH transfers the unique (S)-4-amino-2-hydroxybutyrate (AHBA) side chain, which protects the antibiotic butirosin from several common resistance mechanisms. Butirosin, an aminoglycoside antibiotic produced by Bacillus circulans, exhibits improved antibiotic properties over its parent molecule and retains bactericidal activity toward many aminoglycoside-resistant strains. Butirosin is unique in carrying the AHBA side-chain. BtrH transfers the AHBA from the acyl carrier protein BtrI to the parent aminoglycoside ribostamycin as a gamma-glutamylated dipeptide.	5.95308e-05
NZ_LN831776.1|WP_046501914.1|2138111_2141702_-|hypothetical-protein	gnl|CDD|349463	cd06244, M14-like, Peptidase M14-like domain; uncharacterized subgroup. Peptidase M14-like domain of a functionally uncharacterized subgroup of the M14 family of metallocarboxypeptidases (MCPs). The M14 family are zinc-binding carboxypeptidases (CPs) which hydrolyze single, C-terminal amino acids from polypeptide chains, and have a recognition site for the free C-terminal carboxyl group, which is a key determinant of specificity. Two major subfamilies of the M14 family, defined based on sequence and structural homology, are the A/B and N/E subfamilies. Enzymes belonging to the A/B subfamily are normally synthesized as inactive precursors containing preceding signal peptide, followed by an N-terminal pro-region linked to the enzyme; these proenzymes are called procarboxypeptidases. The A/B enzymes can be further divided based on their substrate specificity; Carboxypeptidase A-like (CPA-like) enzymes favor hydrophobic residues while carboxypeptidase B-like (CPB-like) enzymes only cleave the basic residues lysine or arginine. The A forms have slightly different specificities, with Carboxypeptidase A1 (CPA1) preferring aliphatic and small aromatic residues, and CPA2 preferring the bulky aromatic side chains. Enzymes belonging to the N/E subfamily enzymes are not produced as inactive precursors and instead rely on their substrate specificity and subcellular compartmentalization to prevent inappropriate cleavages. They contain an extra C-terminal transthyretin-like domain, thought to be involved in folding or formation of oligomers. MCPs can also be classified based on their involvement in specific physiological processes; the pancreatic MCPs participate only in alimentary digestion and include carboxypeptidase A and B (A/B subfamily), while others, namely regulatory MCPs or the N/E subfamily, are involved in more selective reactions, mainly in non-digestive tissues and fluids, acting on blood coagulation/fibrinolysis, inflammation and local anaphylaxis, pro-hormone and neuropeptide processing, cellular response and others. Another MCP subfamily, is that of succinylglutamate desuccinylase /aspartoacylase, which hydrolyzes N-acetyl-L-aspartate (NAA), and deficiency in which is the established cause of Canavan disease. Another subfamily (referred to as subfamily C) includes an exceptional type of activity in the MCP family, that of dipeptidyl-peptidase activity of gamma-glutamyl-(L)-meso-diaminopimelate peptidase I which is involved in bacterial cell wall metabolism.	5.23584e-89
NZ_LN831776.1|WP_046501931.1|2160585_2161728_+|DUF1611-domain-containing-protein	gnl|CDD|225902	COG3367, COG3367, Uncharacterized conserved protein [Function unknown].	9.57061e-12
NZ_LN831776.1|WP_020434150.1|2150234_2152073_+|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	2.47824e-56
NZ_LN831776.1|WP_020434156.1|2141987_2142605_+|RNA-polymerase-sigma-factor	gnl|CDD|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	9.53793e-32

Protein sequences

>NZ_LN831776.1|WP_020434149.1|2152050_2153163_+|response-regulator
MYKVMIVDDEPLFRDYLRLKMDWQRHGFRVCCEARNGREALLEAEKHQPHLALVDINMPFMDGIELAVKLKERFERVVIVFISGHNEFEYLQKAVRTGVQDYLLKPFNEEEMSAMLARIRPKLPQLPREREAEQEGAEGNGPGASPAGQEAPDLSSIRDVIVLGLRMKDADILDEVRKAIRQLRGCKWGSEYADAMMMGLVSLVLTFAGERGFSYSRVWDSEGDKSPFERLKACGSWEGAEEWLTALYRRVIQLTEDVKPTKASNLFAAAIQYIEQHYADAELSAEQVAGGVYVDPSYLRRVFRKESGYSIVDHITHIRMKKARVLLLEGNRKLADISESVGYADPNYFSKSFKKRFGVTPTEYEQLVRK
>NZ_LN831776.1|WP_020434150.1|2150234_2152073_+|sensor-histidine-kinase
MKFTALIRRWFGRLRFKSKVIAIFLPLLILSLLILGALSSHLFSRSLIERTTRNVADESQLILSRTDYILRSAETAANIMVTNINRLYESYPAVQAVPLEQFRFANLMQSRLSIDLSIFREVDAAVFVGKDGTVYTSYTSGGEEEAKGIAASGMLNTVREAGSYGYSHWFGMEKRSYLTSNPDSPVLTLGKMVINIDTGEPLGTLFLIVREEQLSAFLQSSDPAASKAYYFVDEHRRVVAAADKSSLLQPLEPSMAARIGDRERADRAASFSYKDDGNLVTVSRFGRMDWELINVVSLKLLTADVQQNVRLTALVGALCLIFSLFGASFLSRMVASPLERLTRAMRQVVSGDLRPVAAARTEDEIGTIAEAFNFMVGRVRELLKKVTEEQKRKREYELALISAQIKPHFLYNTLDTIYVLNELDRNEEARDTTKALADFYRMVLNKGRELIILEKEARITDDYLAIMQIRYPDVFRYEIDIPAELSGTPIPKLSLQPLVENAIYHGLKKKGSKGFIRIQACSTGGKVLVQVTDNGIGMDEERIEAIMSGYSPEEETRSIGTYSVQQRLNLYFGEPYGLTVRSVVDEGTVVELSLPMLGTEKRDEQDVQGDDR
>NZ_LN831776.1|WP_046501919.1|2149056_2150046_-|LacI-family-DNA-binding-transcriptional-regulator
MPTIKDIAREAGVSAATVSRVLNNDLSLAVSEVTRTRVFAVAEQLGYKPARLKQLKRDTERSGKTVSLLLRCSVEEERDDPYYGSIRRGIELRAEELGIVLGQTLRGHGQLPALRACDGLIVVGGFDPRELESLHADPSTIVLVDQYGEQTDYDSVRTHFRQAVEQALGHLMALGHRDIAFIGGGGDGERRAHHFERIMLERGWFDDRLVRTGGWSSADGYRMMNELLAGAKRPTACFAASDPLAVGALRALHGQGVRVPEEMAIVGFDDIEMAAYVQPPLTTVRAYPEQMGKAAVQLLVERFEGREAPSHTITGTKLIVRESCGGTPD
>NZ_LN831776.1|WP_020434152.1|2146670_2148965_-|alpha-galactosidase
MNIYADETLGLFHLQSKDTSYIIQLVEGYPSHVYWGARLRHDNSLAGVLELRERSSFSPIPLLTNPSLSLDALPQEYPQYGTSDFRRPAYQVLLADGTRTTELKYAGYRITSGKPALEGLPALYTEADHEAKTLELTLNDDYTGLTVKLLYTVFADHSAIARSVRFEHNGQAPLRLEQALSASVDFADSAYDTLHLSGAWARERHVQRRRLSAGAAVSLESRRGSSSHQANPFLALLRPGADEDQGDVYGFSLVYSGSFAAVAEVEQFNQTRVSIGINPFDFSWLLEPGQSFQTPEAVLVYSGEGLGGMSRTYHRLYRTRLCRGVHRDKTRPILVNNWEATYFDFDADKIAAIAKEAGPLGIELFVLDDGWFGKRDSDNSSLGDWFEDRRKLPGGLADLAGRVNAEGLQFGLWVEPEMVSPESELYRKQPDWCLHAAGRRRTEARNQLILDLSRPEVCDYLYETLSAVFASAPITYVKWDMNRNMTEIASASASPERQKETAHRYMLGLYDLMERLTSRFPDILFESCSGGGGRFDPGMLFYMPQTWTSDNTDAIERLAIQYGTSMVYPASSMGAHVSAVPNHQVERITSLAIRGDVAMSGNFGYELDLTAFTGAEKRLAARQIAQYKEIRELVQQGDMYRLLSPFEGSGETAWMFVSEDKTEAFVAYFRVLAKPNAPISRLPLKGLDPELDYVIETGAASDDGAADHSGAEGSASAGASGSAFQEGFGGTLHGGDRLMRIGLVVSDLHGDFASCTYRLRAARR
>NZ_LN831776.1|WP_020434153.1|2144801_2146154_-|PQQ-binding-like-beta-propeller-repeat-protein
MGKGQILKTLSGAICAALMLPLGVGGGTAQAEEAAVSIRNPYYQQVEATVVQPAWSLPVAKPKVVNNLEPVTAVAENGKVFMLQPNGKLAALNAASGAKLWEYGSQLAQRMVYNNGAIYGMTTAGALYKVKEDNGSKVWSAALGYGTADSITVTGGTVYVTQGQKMAAVDAATGKVKWRIAEDPNNYYYGSKALEAEGVVVRNYAVSGAITVSLVAVYDKTTGTKLWEASRQQAPLAIKDGVLYSERELFMLDDDPVNRKIQIAAFNLRTGALKGERTYSWTDKAATDGVYHGGGSYSSAFLNGNDLYIHQGQRLVLYDFWNYVSGAEPVKKWAQESYDQRNPLNLVHQDRIYFTDEHSHGLIAMKLANGQYTRFDQGENNTVQAAIFGKGVYVGQSDGLLHAYDLISSKPVFTVRTGSPEFAPLLKTGGMLLVQSGGKLHGIKLPASLK
>NZ_LN831776.1|WP_020434154.1|2143812_2144685_+|hypothetical-protein
MHYRKTLIAMASTALLFGLGYTPAGEAAADNSSAPSAARPAIKAGFKTIALTGEASAKAKTEQEMKKFKNLKDMEKKALSETLKPGEIRYVYINDKEYQASSAGSSTSSAKYSIRYNTYNEYAEKYAAGNTAIPLRLQQQPEGYNLWVAEIAPYLSQKEEAKIYNQVIAEGKASGKKIYVKKLQEKRTTVNLIYNMPSEKNGKRGVLGIVAEPAGPNDKTVESEPATAQSEKLDVGGQEVMYTAIDKMEYKSVAWMNPQTRVNYIIRETRGHLTKEALLALAGQIIEASA
>NZ_LN831776.1|WP_020434155.1|2142586_2143720_+|hypothetical-protein
MCKDELTSEELFLKEGDHSDQLPLVDVHDSVMEAIGLGNNRLMMEHASQLQAGNTSDIMQSMEPVVEAERYRKRTLRRQAGRWAAALVLIASLGGGYFLFVEGPGQAAKFQFEVLPYQPLVVTEEGGKVVRSNRPVSPSEEKVPQIQESKEEKLFRAKYSEAYKAVEKLLLPGEFASYVLRQEKAGGEPPMIGVVNRMMLFKDYSSYVAKAKKYTAPDLKQPEYMPEGYVFDQAVIQPYFEIKEKELLALTGGIKLEGGFRVPWRKEPLDSINFDNSGLSYKKGQTKVDISVKRLKEKTGIIESLLWTKNTSMENILVNGTQLIFMDHSKNGEVKLGYKYKLVWADPENNMLYNLTTTPESSLTKEEVIHIAAGMMN
>NZ_LN831776.1|WP_020434156.1|2141987_2142605_+|RNA-polymerase-sigma-factor
MSRNRRLKCYTCIDSRKETVVDSIEEKIKRIQAGEVYLFSDVIRLYQQRIYVYCFRLLNSREEAEDAVQDIFIKAYQNIWDFKLQANFTSWLYRVSYHHCLNQLRRQKFQNQLRRLLRQDVTAKSAEQVVENRLFSESVAAALQKLSIEERNLVILRIFEDKSFAEIAEILGKSTVTVRKRYERTRSKLRESIVRREKQLCARTN
>NZ_LN831776.1|WP_046501914.1|2138111_2141702_-|hypothetical-protein
MMSKKLLSLLIALTLTLSGILPAAYAGEVAAEAQPQVQTAPASAASGASSTVTAEVYQPAAPTVSTEVYQASMTEARTLPITLALPEGVTANQLTWNFGRTAEEMKPLAQWKKWNNASSVRAYTGDPFIKVSYEPASPSTVTALVYFDMPFGGNLSISGIRAEYVKLAGTYNLTATAPDGHVLVQQQVKLNPYDTYHTYDEIKPAIDRITADSNNKYGRYVEYQQIGTSTQGRAIHFSIVAKDKASVDQYLNETLPLMNNDPAALQEMIKNGQLQNYKVPIWLNNIHADEANGVDVIIKFLDTLMTQKIVNYDTTDAKGNVVPVALDIDKALDNVIFLLDYVENPDGRALNTRATSTLLDPNRDNSYQTQPETQAVTAQIAKWTPLSFLDMHGFVSGFLIEPCTPPHDPNIEYDLVLDNMLEQATAMGNAGIANTKYNAYHIPYLEAEKLKNDPNYANPYGNATGWDDASPAYTAVYAMHQGALGHTIEVPELNEDSLDAFYYAALAATHYVQNNKEKLFLNQLEIFKRGMNNEDHKEVDKYLVNAKYESIGRKRATEATNFFPEYYVLPVAKDLQKNELETYKMVQYLLRNGVKVEQTTTPVTVDGVTYPSGTYVVNMHQAKRGYANLVLYDGLDVSDFNEMYSDTVQNFADMRGFDRYISRTAGAFTGKTQQVSSVVIPTTDLNQYRFEQNYVIRNSNNDAIKAVNELLANKKAVTLLSNGGPGYEQGSFLVSRSNLKTVASKYLLDLVPFSASADKTGKLLKPANVGIAGAPSFILADLGFKVTTDTAVADVLVNAGTSLIAGGKPFIGYGRTMLSSIKSLKILPGLDYSNPVNKSNNPAAHEGLFKATVSQDSVITAPYADNEYLYTVSAAYITAVPEGAEVLAKYGTGEDFFKAGWWPNSDAAKGQVLALNYQKDNIHVTLFANDLLNKYHPQNQFRLLANAIYASSPAATEADGMDNGALEPEPASPSNPGSGAPAATATPAPTATPAPTGAPASPQPTATAAPAPAVHFTDLGRVAWAVSAIEELTAKGILNGVGGNAFAPLKEVTRAEFITMIVRAFDLQTENASATFSDVSAADWSYSYIAAGVSNGLINGVGNGKFEPKRSITREEMAIIAANALTKFKGKSVTNADAALANFKDKSSIAPYGKNAVALLTQEGIVKGMTVSTFAPKGIANRAQAAVIISNIINLQ
>NZ_LN831776.1|WP_046501913.1|2136990_2138019_+|hypothetical-protein
MKSRILPMYEPKLSTYNVYAALFSIIAKDEGYLPWYYSNFISIGINTCDDTLYFTDHFTFFEYGEGSTSCPWLEVYKPPHKTIYSQYSFNIKEVLTGYLNQNQYIWLYLDQYYIPQSTCYQKMHKEHSVLVYGYDEAASVFYIADNLDNGKFIQTVISYQQLIKAWESDICEHFRRLFRVLNSKQGEYTLSATHLRNQIEGYLSSKPIDQGIYWDQIPVDGPHAYVQNIQYWIFGHEVYSYIQQLNKQVQEMKGTKSLDIRIPHLLWEHKKCMAERMHYLNLGKYDLASEYEKVVKHSLTIRNLSIKYNITKNDSILDEIDTRMNEVVHTEDIVLRKLAGLL
>NZ_LN831776.1|WP_046501924.1|2154450_2155776_+|extracellular-solute-binding-protein
MKIEHKRLSALMIAFSMVLALSACGGGNGNTASDQNQDPAAAADSGKVKLKVYAQHFDEDTKGPFDYAVEELKKEMPDVEIELDSAVQDGNQKLKTYAATGNMPDVYFTDWPTLQTFAKSKNVELLDDYESTAQYKQNLNPGVESRLIAPDGHVYAYPDTGIEFQLIYYNKSIFDKVGIAVPIKTIDGLAEAAKKLKAAGYIPMSIFGKEKWISAAFYNGLVTREQAAGFGALEAQGVTELPQAFVTAAEQMKQLQEAGLFDANATNTNYDQASSQFYQGKSAMFVNGQWEIYSSEEKLGDQVDWMYWPAKDEATYEQSKYNIDGAGSPQGYAVSPGSKNKETAVKVAAFLAAKSAEYKYSKLGSPIISPKTDKPIAADVPVMMQRIATELLPNAKEYAKLLSNTQIQNAINDNTQNLLVDGFATENFITNLNRALGKENQ
>NZ_LN831776.1|WP_020428886.1|2155850_2156729_+|sugar-ABC-transporter-permease
MNKYLGNKSALALFLLPALLLYSVILIYPVLQTVVRSFYDWDGLSTAAFSGIANYRELFNDPLLSTSLKNGLIFALVLAGFQIGLGTVLALVCANPRTRGRKLLKTAYFIPVVLSVTVVCQLWIAMYDPTNGLVNKLFELLNIPYRQNWLSSPTQSIIAIAFVNAWQFMGYQFSLLYAGVKAVPEDYFEAATIDGCGKWRAHWHVTLPLMRETYKFCFTIAITSGIGAFVQMLIMTNGGPGTTNYTMTFMIYRYAFMESNYGYACAVSVLLVLISLIATVVINKVFDRGQNA
>NZ_LN831776.1|WP_020428888.1|2156752_2157595_+|carbohydrate-ABC-transporter-permease
MSPKTFRSIGQFLLQIPLWLYFAVSIYPLFWMISYSLKNNDEIFVTNPFGLPTHFRFENYINAWTQFNIPRYFWNSFVVSIISTVFILLLALMFAFAVARMQWRFRSAVRTYMLVGMFMPLQVIMIPLALLVRDFHLTNTYGALIIPYIAIGLPFSTMVFYGFLVSIPREIEEAACIDGASIYRLFLGVILPLALPAIATIAIFQFLNNWNEFTLAYILISDENMKTLPLGLLFFQGSYSTDWGAMGAVMTIASLPMVLVYLLLSDQVERAMTVGSAVKG
>NZ_LN831776.1|WP_046501928.1|2158161_2159427_-|MFS-transporter
MTEPVIASQAAPAVHSYPKLWANKKFMLLLCSFSISLFGNTFHSIALSLWVLQTTGSAKLVAVLTIINLLLSSLLGSIGGTFADRTNRRKIMLITDLVSCSLVVTLALVLSVPSASFIIVAVLTALTTVSALFQSPAYQSSIVTVVGKEHVQQAVGMLNLSENICRTVGFSVGGIFVAAFGAADAILFDGATFLVSFLLVLAVRSLPMPARANPEPQQKKKFIQDLGEGIRYIWKFPFAKAVIIMLPTLTLFFMPSMMLTQVMAVNVWKSSPFQFGLMEACIPLGYMVGSGLIMILGSKIRRRGLLIMTGLLCLGPMYILLSFITSAAAAIPVVLLIGFMFSFCTLLINIVLRLEISEEIQGRVFGVLGSIMSVAPSIGLSVVSYLSDHFSPGPVMGSIGLLLLLFALYTSTKLKIIRGYR
>NZ_LN831776.1|WP_020427653.1|2159475_2160387_-|LacI-family-DNA-binding-transcriptional-regulator
MKKTTMKDIAIRANVSVATVSYVLNRVDNQTIPEKTRRQILQLAEELHYIPNLAARSLANQKTGLVGVLVHRSRQLPYWKLHAQLAFIHTLEQRLTAAGYHTLLYSLDTGNPSLDIIVERKLEAVFLIDAQDASFYSISRHFVEGIPLILIDSMIEDKLFKQVVYNYRSALEKALPDDLSQVCLIMESFNNSLLTRYIRSCVPLSDDAVFEIRELQDLLSATAHHRFKQAIVINEFIGSYVEKSGDFEHLTVICTCNSPQMLGERVEKILFQGDKAEVAFELMQELLYHPDYSEQENNCYYVD
>NZ_LN831776.1|WP_046501931.1|2160585_2161728_+|DUF1611-domain-containing-protein
MDNVVLYPFNKITQGIIRFRDLTDFTVRAVIDFVLHKGKDAAELVEGQAAGIPITDNFEEMFGIADTLILNDPGTSFGNNEGVYGEHNLSQLWRLLVASAHEHKLRIISVHEIIDRPTLDWLLKNGITIEILPQIPASLQHRLHTEYIFPSPGDEVATYLSYFDIDAQITAYNRNICKVGIFATRGCLGKFTAQMSLFRALRQAGEKVQAIITEPTAALFNQPGGDIMKFIAHNPLNQYPYYIHAAVREAESTGCDYVLLSGQGSLLPNENFVIAATKVSYLRALQPDLTILIAGYDDDEQIRDSLDILRIYGNASRPFAILIPDKYEVDFGEYISKTPEEIEQRKEEIRSRFDAAHVESVLDIGRLAGKLANYKKTVRL
>NZ_LN831776.1|WP_020427652.1|2161747_2162887_+|DUF1611-domain-containing-protein
MKRVVLYPFNKITQGLLRFRDLLDVEIVSVIDFVEEDGQDAGAQVDGKHSGILIHSSMADGLKDADTLILNDPGTTFGGNSSVFAEHDLAGLWRELVLYASGRGLKVVSVHEIYDRATLDWMAEQQIQIDVVHSPREQLFQEMDKRYGTGGTDIERYLEQFEKEALMFSRPRSIKRVGIFATRGCIGKFTVQMNLYRQFAAEGIPATAFITEPTGFLFGQPEGDIFKFLAQRPLEQYPYYIDTVIHHAQDSGSDWIIMAGQSSILPTMNIAFNSLRYAMLRAFDPEYVLLIADYDDDGAIHDAIEMLRIYSRRPLALLLPDKLETSYGQYEIYPHERRMARKLELEQKFQIHVLFIEQAEAALNLLLEEADAIPAGSGK
>NZ_LN831776.1|WP_052741430.1|2162889_2163993_+|hypothetical-protein
MLHPGECIYQIVTDRFCEGNPAGLPVVYYGTEQYMSGGDDPHNRAMMSSFSRETTAYRLVAQLNRLRACNLAIGYGSTKLLYVNSGVLVFERSCKRDVALILINQEDNAQILPSLATSLPQGAYSSLLKDIYPDHPAVAGAEGDMQNVMLAPRSAFVYSYESDLEKPAAVHVYPKAAAPGSEFIIRGRHLGDTGCLTVGGCEAAVISWQSGKIVARVPAVPAGVHPVQGLSEGGQKFRLPEELKVWTGMLVTVRLVLKNVHTDFDTRVYVTGNVYELGAWQAERAAGPFYNQIVYRYPTWYCDISLPADSRIEFKIMLRSGSGMMRLEQGEAHCFHTPAEGVSEIIAEWQGACQESFQLSEGDAAYG
>NZ_LN831776.1|WP_020427650.1|2163985_2164420_+|hypothetical-protein
MDERLQFDGTHLTFQTALDEERRRLIAWHFKSSWLELQQAVRLTTLSSENKFAQFLFPVDRPLGQTLEMRVPRPGSRYYYADLGIIKKVQTFVPILRSNVLFICDDGSPMYSDWFSFQRDHASPPLLEQNTWWEFFTGYSLSAH
>NZ_LN831776.1|WP_020427649.1|2164441_2165620_+|glycosyltransferase-family-4-protein
MQSSTSVLILSWEYPPVVIGGMAPHVYELSRHLACGPAEVHVITNSAPGRPVLEVENGVYVHRVNSYENLTDFEDWVLEFNLAIVDYVASRLSGNVRLDLIHAHDWLVGYAALLLHQRLGLPLVTTIHATEFGRNQGLFTPQQHMIHAIEHELVTSSDKVIVCSMHMQREVCTVHGLDKSRTEIIPNGIDLCSLELIPAHSFRREHYAQDGGKIVLFIGRLVKEKGVQVLLQSIHEVLREFPHCTCIIAGRGPMSAELEDRAAELGTSIRFTGFVDSQEKSFLLQLADVCVFPSLYEPFGIVALEAMGSGTPVIVSEAGGLAEIVEHGRTGLTSMSGDPGMLAARILQLLRDPDEGSLLAEAARREVLLRYDWQPIADRTGEVYSTLSGVRL

Crispr_ID: NZ_LN831776_28

• CRISPR_ID: NZ_LN831776_28
• CRISPR_location: 2168753-2168827
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_28

Consensus_repeat	Method
AATTAGTGTCCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_28

>28.1|2168776|29|NZ_LN831776|CRISPRCasFinder
CATCTGCCCGAGGATAGGGTACTCCGGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_28

CRISPR arrays

The CRISPR arrays of NZ_LN831776_28

>merge|NZ_LN831776|28|2168753-2168827|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTTCATCTGCCCGAGGATAGGGTACTCCGGCAAATTAGTGTCCCTTTTTCCACTT

>NZ_LN831776|28|30|2168753-2168827|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTT	CATCTGCCCGAGGATAGGGTACTCCGGCA
AATTAGTGTCCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020427649.1|2164441_2165620_+|glycosyltransferase-family-4-protein	unknown	unknown	gnl|CDD|340831
NZ_LN831776.1|WP_046501935.1|2165637_2166876_+|4Fe-4S-binding-protein	unknown	unknown	gnl|CDD|223966
NZ_LN831776.1|WP_020432016.1|2171639_2173211_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270298
NZ_LN831776.1|WP_020432451.1|2182380_2183349_-|alginate-lyase-family-protein	unknown	unknown	gnl|CDD|377511
NZ_LN831776.1|WP_020432015.1|2173234_2174134_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_LN831776.1|WP_020427647.1|2166832_2168203_+|3-phosphoshikimate-1-carboxyvinyltransferase	unknown	unknown	gnl|CDD|235037
NZ_LN831776.1|WP_020427653.1|2159475_2160387_-|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_LN831776.1|WP_167345595.1|2169007_2171335_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_046501940.1|2175092_2179619_+|hypothetical-protein	unknown	unknown	gnl|CDD|379079
NZ_LN831776.1|WP_052741431.1|2179720_2180629_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379240
NZ_LN831776.1|WP_020427652.1|2161747_2162887_+|DUF1611-domain-containing-protein	unknown	unknown	gnl|CDD|225902
NZ_LN831776.1|WP_046501928.1|2158161_2159427_-|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_LN831776.1|WP_020428888.1|2156752_2157595_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_082118085.1|2183385_2184516_-|glucuronyl-hydrolase	unknown	unknown	gnl|CDD|369381
NZ_LN831776.1|WP_020432458.1|2180833_2181826_-|YiiG-family-protein	unknown	unknown	gnl|CDD|372366
NZ_LN831776.1|WP_046501931.1|2160585_2161728_+|DUF1611-domain-containing-protein	unknown	unknown	gnl|CDD|225902
NZ_LN831776.1|WP_020432444.1|2184633_2185518_+|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_052741430.1|2162889_2163993_+|hypothetical-protein	unknown	unknown	gnl|CDD|99882
NZ_LN831776.1|WP_020432009.1|2174153_2175023_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_020427650.1|2163985_2164420_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020427649.1|2164441_2165620_+|glycosyltransferase-family-4-protein	gnl|CDD|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	9.60982e-90
NZ_LN831776.1|WP_046501935.1|2165637_2166876_+|4Fe-4S-binding-protein	gnl|CDD|223966	COG1035, FrhB, Coenzyme F420-reducing hydrogenase, beta subunit [Energy production and conversion].	7.65462e-43
NZ_LN831776.1|WP_020432016.1|2171639_2173211_+|extracellular-solute-binding-protein	gnl|CDD|270298	cd13580, PBP2_AlgQ_like_1, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	2.49871e-121
NZ_LN831776.1|WP_020432451.1|2182380_2183349_-|alginate-lyase-family-protein	gnl|CDD|377511	pfam05426, Alginate_lyase, Alginate lyase. This family contains several bacterial alginate lyase proteins. Alginate is a family of 1-4-linked copolymers of beta -D-mannuronic acid (M) and alpha -L-guluronic acid (G). It is produced by brown algae and by some bacteria belonging to the genera Azotobacter and Pseudomonas. Alginate lyases catalyze the depolymerization of alginates by beta -elimination, generating a molecule containing 4-deoxy-L-erythro-hex-4-enepyranosyluronate at the nonreducing end. This family adopts an all alpha fold.	6.39382e-37
NZ_LN831776.1|WP_020432015.1|2173234_2174134_+|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	8.96972e-116
NZ_LN831776.1|WP_020427647.1|2166832_2168203_+|3-phosphoshikimate-1-carboxyvinyltransferase	gnl|CDD|235037	PRK02427, PRK02427, 3-phosphoshikimate 1-carboxyvinyltransferase; Provisional.	1.80296e-129
NZ_LN831776.1|WP_020427653.1|2159475_2160387_-|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	2.10752e-29
NZ_LN831776.1|WP_167345595.1|2169007_2171335_-|helix-turn-helix-domain-containing-protein	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	8.11768e-27
NZ_LN831776.1|WP_046501940.1|2175092_2179619_+|hypothetical-protein	gnl|CDD|379079	pfam13229, Beta_helix, Right handed beta helix region. This region contains a parallel beta helix region that shares some similarity with Pectate lyases.	1.1014e-10
NZ_LN831776.1|WP_052741431.1|2179720_2180629_-|GNAT-family-N-acetyltransferase	gnl|CDD|379240	pfam13527, Acetyltransf_9, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	2.76753e-12
NZ_LN831776.1|WP_020427652.1|2161747_2162887_+|DUF1611-domain-containing-protein	gnl|CDD|225902	COG3367, COG3367, Uncharacterized conserved protein [Function unknown].	1.80276e-14
NZ_LN831776.1|WP_046501928.1|2158161_2159427_-|MFS-transporter	gnl|CDD|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	4.7907e-55
NZ_LN831776.1|WP_020428888.1|2156752_2157595_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	4.36676e-77
NZ_LN831776.1|WP_020432458.1|2180833_2181826_-|YiiG-family-protein	gnl|CDD|372366	pfam12889, DUF3829, Protein of unknown function (DUF3829). This is a small family of proteins from several bacterial species, whose function is not known. It may, however, be related to the GvpL_GvpF family of proteins, pfam06386.	1.82687e-67
NZ_LN831776.1|WP_046501931.1|2160585_2161728_+|DUF1611-domain-containing-protein	gnl|CDD|225902	COG3367, COG3367, Uncharacterized conserved protein [Function unknown].	9.57061e-12
NZ_LN831776.1|WP_020432444.1|2184633_2185518_+|AraC-family-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	6.99974e-27
NZ_LN831776.1|WP_052741430.1|2162889_2163993_+|hypothetical-protein	gnl|CDD|99882	cd05807, CBM20_CGTase, CGTase, C-terminal CBM20 (carbohydrate-binding module, family 20) domain. CGTase, also known as cyclodextrin glycosyltransferase and cyclodextrin glucanotransferase, catalyzes the formation of various cyclodextrins (alpha-1,4-glucans) from starch. CGTase has, in addition to its C-terminal CBM20 domain, an N-terminal catalytic domain belonging to glycosyl hydrolase family 13 and an IPT domain of unknown function. The CBM20 domain is found in a large number of starch degrading enzymes including alpha-amylase, beta-amylase, glucoamylase, and CGTase (cyclodextrin glucanotransferase). CBM20 is also present in proteins that have a regulatory role in starch metabolism in plants (e.g. alpha-amylase) or glycogen metabolism in mammals (e.g. laforin). CBM20 folds as an antiparallel beta-barrel structure with two starch binding sites. These two sites are thought to differ functionally with site 1 acting as the initial starch recognition site and site 2 involved in the specific recognition of appropriate regions of starch.	3.00084e-33
NZ_LN831776.1|WP_020432009.1|2174153_2175023_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	3.1907e-59
NZ_LN831776.1|WP_082118085.1|2183385_2184516_-|glucuronyl-hydrolase	gnl|CDD|369381	pfam07470, Glyco_hydro_88, Glycosyl Hydrolase Family 88. Unsaturated glucuronyl hydrolase catalyzes the hydrolytic release of unsaturated glucuronic acids from oligosaccharides (EC:3.2.1.-) produced by the reactions of polysaccharide lyases.	4.71938e-32

Protein sequences

>NZ_LN831776.1|WP_020427647.1|2166832_2168203_+|3-phosphoshikimate-1-carboxyvinyltransferase
MGLVRNRVGLPAKCDLQIKAKREVCSFEFHSVPGDKSISQRAIVLNAIAEGQGTVYNVLRSRDIESCITILRQLGVRIAWNGDELSVHGQGLRGLQAPAGRLEVGNTATSARLMLSVLAGQSFAAELGGNALLSARPMDWVVQPLTDMGAVIEYLGAKGCLPLRIQGASPLSPIDMEATVFSAQEKSALLFAGLYAEGITRYRQRCQSRDHTERLMHYFGIDIHSDNDVTFLKGGNAFCAKDVMVPGDMSSAAFLLAAYAIRGVDRKGSLLIKQVGVNPTRSGFIRLLAEMGLHLTLQAEAELISGEPVADIYCTPGTRLSSVLAEGNGRIQSLIDEVPLLAAVSAFAEGNTVIRDCGELRDKDTNRIQTTAGVLKAFGVETSCSDDEMVIHGGRPLSPAIVNSCGDHRIAMTAAVLASSLDEPSIIRNCGCINVSYPGFVEDLSQFAHIDVLPAE
>NZ_LN831776.1|WP_046501935.1|2165637_2166876_+|4Fe-4S-binding-protein
MTSFITLKEEIIDLSLCASCGLCAAVCPQGLLAMNGDSVSLPVFQGLESQAEDTCGSCNLCSEVCPGYDTGVMESERRIFGRNRSELERWTGIYLSTHQFSAADPEILGRAAAGGAGTILAVTALEEKLADAVIVVGRDEERPWVPKAYLADSVERIIECAQTSYCITPNLDLLQDDRYDKIGIIGVPCQIQGIHKLLNLPEHLPSSVLADKVAFTIELGCASSTSLGGTEHLITEILGIELADVAVMRYREGQYPGQFMVKTRQGQEHYLPFYRLVEEFKKFKTFRCLACPDWWSGIADISISDGDPNIFDSSKEGISAKASSTVMVRTKTGARLLELAVRRNAARLVDYTFDNNLGLERKRQRYRSYAAMGDRRIPLAPGRDMDYSQILSDDEVIRIGIGPKQGRPAGQM
>NZ_LN831776.1|WP_020427649.1|2164441_2165620_+|glycosyltransferase-family-4-protein
MQSSTSVLILSWEYPPVVIGGMAPHVYELSRHLACGPAEVHVITNSAPGRPVLEVENGVYVHRVNSYENLTDFEDWVLEFNLAIVDYVASRLSGNVRLDLIHAHDWLVGYAALLLHQRLGLPLVTTIHATEFGRNQGLFTPQQHMIHAIEHELVTSSDKVIVCSMHMQREVCTVHGLDKSRTEIIPNGIDLCSLELIPAHSFRREHYAQDGGKIVLFIGRLVKEKGVQVLLQSIHEVLREFPHCTCIIAGRGPMSAELEDRAAELGTSIRFTGFVDSQEKSFLLQLADVCVFPSLYEPFGIVALEAMGSGTPVIVSEAGGLAEIVEHGRTGLTSMSGDPGMLAARILQLLRDPDEGSLLAEAARREVLLRYDWQPIADRTGEVYSTLSGVRL
>NZ_LN831776.1|WP_020427650.1|2163985_2164420_+|hypothetical-protein
MDERLQFDGTHLTFQTALDEERRRLIAWHFKSSWLELQQAVRLTTLSSENKFAQFLFPVDRPLGQTLEMRVPRPGSRYYYADLGIIKKVQTFVPILRSNVLFICDDGSPMYSDWFSFQRDHASPPLLEQNTWWEFFTGYSLSAH
>NZ_LN831776.1|WP_052741430.1|2162889_2163993_+|hypothetical-protein
MLHPGECIYQIVTDRFCEGNPAGLPVVYYGTEQYMSGGDDPHNRAMMSSFSRETTAYRLVAQLNRLRACNLAIGYGSTKLLYVNSGVLVFERSCKRDVALILINQEDNAQILPSLATSLPQGAYSSLLKDIYPDHPAVAGAEGDMQNVMLAPRSAFVYSYESDLEKPAAVHVYPKAAAPGSEFIIRGRHLGDTGCLTVGGCEAAVISWQSGKIVARVPAVPAGVHPVQGLSEGGQKFRLPEELKVWTGMLVTVRLVLKNVHTDFDTRVYVTGNVYELGAWQAERAAGPFYNQIVYRYPTWYCDISLPADSRIEFKIMLRSGSGMMRLEQGEAHCFHTPAEGVSEIIAEWQGACQESFQLSEGDAAYG
>NZ_LN831776.1|WP_020427652.1|2161747_2162887_+|DUF1611-domain-containing-protein
MKRVVLYPFNKITQGLLRFRDLLDVEIVSVIDFVEEDGQDAGAQVDGKHSGILIHSSMADGLKDADTLILNDPGTTFGGNSSVFAEHDLAGLWRELVLYASGRGLKVVSVHEIYDRATLDWMAEQQIQIDVVHSPREQLFQEMDKRYGTGGTDIERYLEQFEKEALMFSRPRSIKRVGIFATRGCIGKFTVQMNLYRQFAAEGIPATAFITEPTGFLFGQPEGDIFKFLAQRPLEQYPYYIDTVIHHAQDSGSDWIIMAGQSSILPTMNIAFNSLRYAMLRAFDPEYVLLIADYDDDGAIHDAIEMLRIYSRRPLALLLPDKLETSYGQYEIYPHERRMARKLELEQKFQIHVLFIEQAEAALNLLLEEADAIPAGSGK
>NZ_LN831776.1|WP_046501931.1|2160585_2161728_+|DUF1611-domain-containing-protein
MDNVVLYPFNKITQGIIRFRDLTDFTVRAVIDFVLHKGKDAAELVEGQAAGIPITDNFEEMFGIADTLILNDPGTSFGNNEGVYGEHNLSQLWRLLVASAHEHKLRIISVHEIIDRPTLDWLLKNGITIEILPQIPASLQHRLHTEYIFPSPGDEVATYLSYFDIDAQITAYNRNICKVGIFATRGCLGKFTAQMSLFRALRQAGEKVQAIITEPTAALFNQPGGDIMKFIAHNPLNQYPYYIHAAVREAESTGCDYVLLSGQGSLLPNENFVIAATKVSYLRALQPDLTILIAGYDDDEQIRDSLDILRIYGNASRPFAILIPDKYEVDFGEYISKTPEEIEQRKEEIRSRFDAAHVESVLDIGRLAGKLANYKKTVRL
>NZ_LN831776.1|WP_020427653.1|2159475_2160387_-|LacI-family-DNA-binding-transcriptional-regulator
MKKTTMKDIAIRANVSVATVSYVLNRVDNQTIPEKTRRQILQLAEELHYIPNLAARSLANQKTGLVGVLVHRSRQLPYWKLHAQLAFIHTLEQRLTAAGYHTLLYSLDTGNPSLDIIVERKLEAVFLIDAQDASFYSISRHFVEGIPLILIDSMIEDKLFKQVVYNYRSALEKALPDDLSQVCLIMESFNNSLLTRYIRSCVPLSDDAVFEIRELQDLLSATAHHRFKQAIVINEFIGSYVEKSGDFEHLTVICTCNSPQMLGERVEKILFQGDKAEVAFELMQELLYHPDYSEQENNCYYVD
>NZ_LN831776.1|WP_046501928.1|2158161_2159427_-|MFS-transporter
MTEPVIASQAAPAVHSYPKLWANKKFMLLLCSFSISLFGNTFHSIALSLWVLQTTGSAKLVAVLTIINLLLSSLLGSIGGTFADRTNRRKIMLITDLVSCSLVVTLALVLSVPSASFIIVAVLTALTTVSALFQSPAYQSSIVTVVGKEHVQQAVGMLNLSENICRTVGFSVGGIFVAAFGAADAILFDGATFLVSFLLVLAVRSLPMPARANPEPQQKKKFIQDLGEGIRYIWKFPFAKAVIIMLPTLTLFFMPSMMLTQVMAVNVWKSSPFQFGLMEACIPLGYMVGSGLIMILGSKIRRRGLLIMTGLLCLGPMYILLSFITSAAAAIPVVLLIGFMFSFCTLLINIVLRLEISEEIQGRVFGVLGSIMSVAPSIGLSVVSYLSDHFSPGPVMGSIGLLLLLFALYTSTKLKIIRGYR
>NZ_LN831776.1|WP_020428888.1|2156752_2157595_+|carbohydrate-ABC-transporter-permease
MSPKTFRSIGQFLLQIPLWLYFAVSIYPLFWMISYSLKNNDEIFVTNPFGLPTHFRFENYINAWTQFNIPRYFWNSFVVSIISTVFILLLALMFAFAVARMQWRFRSAVRTYMLVGMFMPLQVIMIPLALLVRDFHLTNTYGALIIPYIAIGLPFSTMVFYGFLVSIPREIEEAACIDGASIYRLFLGVILPLALPAIATIAIFQFLNNWNEFTLAYILISDENMKTLPLGLLFFQGSYSTDWGAMGAVMTIASLPMVLVYLLLSDQVERAMTVGSAVKG
>NZ_LN831776.1|WP_167345595.1|2169007_2171335_-|helix-turn-helix-domain-containing-protein
MSALPGYRSIKHNTMFVKLLLSLTAIAVITVILISTVTYSISADNSIQNAIAYNESILTQQQELIHKELTAIKYAASGMITTQSYLYHTNGSGKLSVSSMIDLSNFVEAQKKISPYIDSIYLYYAPLELVLTSRPEIRTSPISTFADRSWLEVWKQQSDNRTLWLTGRMDGFEPDQPAASLLQKMPLIGQVNGAIVMNLKLQLLFDDYLSHYHNKKGATLVLGPHSELLYSDSADGDSLLAQLDPARLTGGSGYYMDDSDRIVSYTTSELTGWRFVDITKRSSLLQGMDRIKFIVVTVAATYLTVAFAISFYLSRRLYRPLQSVISYIGGSEAGQRGGSGSPLPAGDEAGFIRHIYDQLVRNWETLMTEKRKVDSLLTDNHTAIKEKYLNGLIQGDSTDQAAELLGLRLDFTRFAVLTLELEEPYPVKGPDGIQFYLFRYGLMEELGADIDGEIFAKDDKRTVILLNVPAEEDDFPLEQAKRLKQLLLTRYSLNVTIAVSRNYSGEQSVCSAYEDTLEALNLKMYIGKGEILPYGILGDWKSQEEAYYYPYELETKLLQALLQTDKEQCFGAIRQITRTAIDRKLGKANIQQLFFQLSGEIMKTLVQTRGDMSAVFGDRPAYADVLSRAETLPDMEECLLDMCGRIIAYHKEKRSKMTDVTLQLATDYMDVNFNKNISVDTVAEHVQRSSSYLSRIFKESTGMTINDYLIQLRIKRAMELLQLDLTIEEICRDVGYANVSYFNKIFKARTGQTPGQYRQQQAADRLLSQRKEQAE
>NZ_LN831776.1|WP_020432016.1|2171639_2173211_+|extracellular-solute-binding-protein
MQMKLKKFSKTLLPAMLTAGLLAGCGGNGGNNAAAPDASAGANAGTKAEAPMEITWGIHLQAPGVVENSQVQKWLEEKFNVKIKPVKVTDASIASGEVPDIFMLGDPANVTAYQNQGVLMNLDQNMLKEKMPEYYADIEKNNALFQTVTIDDKLWAIPMFIDLKPYDLGMLWRKDWLDKVGITKAPETLDEFEKAIYAFAQKDPDGNGQKDTYGLTGTATSTWSSGFYSIFGAFGVEPTMWHEKNGEIMNGSVMPETKEALAKLRQWFADGVIDPEFITDTQDSYRKKLYNNRIGVIEEQIAKGALPDAATVTEMKSLNPSAELVFTKNPKGPGGDGSWDWGVKSNFIVISNKVKDQPEKLNKLFEILRAESTDEETINMTSLGVKGTHWDFTESGATSGATQFKAGFEKAEERDQAGIRLFSLGNITTQAYREKYSNPALNEAIKTYSSAPRQTDALLFSALPSDGKYKNDLTSLMQKYFAQIISGEIPLEDFDKFVAEWKSRGGDELTKEANEMYQAQFKK
>NZ_LN831776.1|WP_020432015.1|2173234_2174134_+|sugar-ABC-transporter-permease
MKTIRKHGELLALFLFAFAFFIVFKYGPLYGVVIAFKDFKVVDGIWGSPWVGFQHFQELFQSSDFYRLLKNTLLLNFYQLVFAFPAPIILAILLNEVRSRYFQRFIQTTMYLPHFVSWVIMSGLLIYFLSPTTGIMADIMGWFGKEPIFFMGKKEYFRSIVVGSSILKDLGWGSIIYFAALSGINPEIQESAIIDGANRWQRIIRINVPSIMPTISIMFILSLGGFLSANFEQIINLLNPVTFETGDVIDTYVYRVGLQQFQYSYTAAIGLFKSLVGLVLILGANLTVKKLSKGENGLW
>NZ_LN831776.1|WP_020432009.1|2174153_2175023_+|carbohydrate-ABC-transporter-permease
MKTRKWQDLITPAIIYLVLSLLALIVVYPFIHVTAVSFSGRGEALRSGFHFFPRDFEWRAYRELLEYPFIWSGYANTVFRMVVGTLLTLLVTVCAAYPLSRPDFPMKRVLIMLILFTMIFEGGIVPNYLLIKELHLLNSRWVYVLPTAANAFQVLVMLSFFRSIPDALIEAARIDGARDMRILFRIVLPLSIPSLVTIGLWSLVHHINAFMDNLLYVTDQSKYVLQQVVRQILIENKLDPFTTATNLTPPAPESLKMASVIVCSLPVLVLYPFLLKYFEKGTMIGSVKG
>NZ_LN831776.1|WP_046501940.1|2175092_2179619_+|hypothetical-protein
MKKRTFIVLSIIALIVGCFPAAAIQAEESHSSEAVYYVSENGSDSNSGTKDKPFLTLEKARDAIRQLKQGAGLPDGGVTVYLRGGTYNRTGSFLLEEQDSGTADKPVTYKAYPGESVRLSGGRQLQKGWFTPVTDPSVLNRIISTDARSKVLQADLKGHGITDYGVMSRHGYYKANDVSQTPPMELYIEGEGMTLARWPNKGTVQMGNIIDPGPTRKDADLQTRGGTFTYTYERPDLWTQADDIWLDGIFGYSWEWSYNKIASIDTQNKSITLAYGEMSGLFKNWYPDFHFAQNLLEEIDMPGEYYIDRSKGKLYFMPTAAFQAANPEITVSMLKTPMISTLNTSFVTFEDLILENGRDSGAVIMGGDSVRLVHCEIRNFTEGGVRINTQSRWLYNDFAKGTGVNHAIVSTHIHHVGGTGVILNGGDRLTLAPGNNVVENSHIHDFAYYHKAYNPAVILTGAGNRISHNEIHDAPHPGILIFGNDQVVEYNNIYDVCKTFSDLGAIYMNLGAAPQERGSVIRGNYFHHIGESKAGVQGVYPDNFTMGMTIEQNIFYRMGNSAILNNGGSHIRTKNNLFIDAKVPYEYSDMYLGDGPEQQINKNYMQPWHALFEKYNNFAGMPHLTKYPELADFFTENRYYPDTNTFQNNVIYNPTKTRGPNLNENGAYDKLKLVQYANNWVTDRDPGFVNLAGGDLNLKANAEVFQQIPGFQTVPFSEMGIIGKAGPYLAPDVIPVKGVVLYEDAVTLGIGKTYSLYSAVLPWNATNNKLQYTSSDPSVVKVDADGKLKGVNLGNAVITAASADNPLLKDEVQVTVEVGDGIMDETTFENGRNSWPMDANRTIVETDGGNHMYKLLKGATTLNENDFSNYELTFKLKTPPVIPESATLYVFDRLNPGGSGGRIGYKKLADGTSSWILYNAAWGTVKQNTLATQDLLPDTVYTMKIIVKGHEISVYLDGKLKLKGTDPTSNPSGKVGFYAGGFDYLLFDDIKFTVPTKDVAGLLLDKSSVNMVMNEQQQLQVQFDPSDAENRAVVWKSSHPEIASVDGNGTVTALGTGEAVVTVASAVNPSASASARIVVSNILHFTDYDTGANGWPVDPNRSIVTVNGNKMYKILKGASALHPKLFTDYDLTFKLKTPADMPEAGTFYVYDRTASGNSGKIAYKKLADGTSQWILYSPNWTVLQTKNFAAADLQPDTEYNIRVLAEGSSIRVYVNGELRLDGTDSAHNPSGTVGFYVGGFSAMWIDDVKFTMIDRAAPVTTAVMTPALPDGSDGWYTHPVTVELKASDTDSGVTDTVYSVNGGTDWLPYQGPVTFSRDGRYSVQYRSVDSAGNTGDIQTLSFKLDGSAPELTVAEPAARAYAGAETLTLSWTAADVISGVADGKTAALLDSEAVEQGASVPLYTLDLGSHTLAVSASDGAGNTQERTVTFSTYADVHSLKALVSLFRQKSWIDNHGIANSLSTKLDHGQVEAFIHQVQAQNGKHIQSEAASYLLRDANDILGRVGTQD
>NZ_LN831776.1|WP_052741431.1|2179720_2180629_-|GNAT-family-N-acetyltransferase
MFSNENIDIDEIDLINDYKDRKVYRDSFNDLASLVFDLNFEDWYQKGFWDDRYICHSFIREDVVIANVSVSKMDLLINGSNKKAIQIGTVMTHPDFRGKGLSGKLMRHVLDIYEHDCDIFFLFANSTVIDFYPKYGFKSVGESQLKLKYYPTPHADTTLRKLNCSNKEDLAFIKKMVLSRRPVSDQFGVSNNQGLFMFYAIKVFPESIYYSQEDEAIIVYQQEDHVLNLYDVVSQSYVNLNRLINRIANEQTGYIHFHFTPDPFTDKVPYEWMDNNGDVLFIKSNFTLDKNSKFCVPLLAHA
>NZ_LN831776.1|WP_020432458.1|2180833_2181826_-|YiiG-family-protein
MRKLSFVIAVILLGAMLSACSAITSTVDQAPAGVTSGERKEIDKYNAYVGLNNLMTGRINEVLVHYFEKFGVDTQPVIEKNFSFIMLDVAETEREVVDKANGYTASQPAFADADPLVIKLTPVIKDLLSVLDDMKAYYDTRGYVDDDFAKGKQLHTKVVSANIAYETVANQYFTALQKLGNEQRLAELQKLKDADQQIRYNALKFMIDAEATAIEMDEQGITAGNVLQLDMTKFKAKYDIMTADLSALMTILKDKERIQKEGINSFSIESYVHSATEAKAAASKIIERINKKEPVSDSDLNGQFLNTTDGTPENFNYLLSKAVERYNEMN
>NZ_LN831776.1|WP_020432451.1|2182380_2183349_-|alginate-lyase-family-protein
MNTQPALQQLLQVANDSMSVSCHAVPAWDIPGFYFDMAGHQAAKRLMEEDAQAACTTALAFGHTGRAEYADKALELIDGWAAINKVLTGDDGPLVSAYLGTGLIQAAGLLQGYSGWRKENQDQFIAWMTGVCLPEWDRIPLRNNWWSWSLYAQLSLFRLMGDQARFAEEVANLKEHIDSSLETSGLIPEETTRGSNAVWYHYFSLAPLTAAIKLVADTTGENLFHWTSPGGKSVKKALDTFFYYADGRIAEWPYGDAQKFPAPLASDTWPLDLYEAMSRIYSDPEYERFVSPYRPITGNKNINSGYYQSYAWIFPELQFTPG
>NZ_LN831776.1|WP_082118085.1|2183385_2184516_-|glucuronyl-hydrolase
MWAQAIEDALRVVSHNIERFGDKFPVTSTQGDRIYRLTPGNDWTEGFWTGMLWLSYEYSRDPRFRTAAMTTLDNFRERLEHRVGLEHHDIGFLYSPSIKAHWILERDESSRSAALQAADVLLERWREIPGILQAWGPKNDPENGGRIIIDCLMNLPLLHWAYQQTGREAYRQAAEQQTAMSRRFLVRGDDSTYHTFYFDPVTGDSIRGGTHQGSRDGSTWTRGQAWGIYGFALAYRYMRQPGLLETSKRLARYFVDRLPEDSVVFWDFDVPQIPETKRDSSAAAIAASGMLELVELLPEHDADREWLAQAARRIVASLAANYSTKGEPDAQGLLNRGSYAVRLDISPDDYVIWGDYFYLEALMRLERGVPGYWYER
>NZ_LN831776.1|WP_020432444.1|2184633_2185518_+|AraC-family-transcriptional-regulator
MASHIEHVDPGHSSFFLAFRDELQEDHFHKFHAHQGLELLFIHEGQGIVEVEGRTYELQGGSLFCFQPYQLHKVEIPAPRDARDVRYVRTNLTFEPRYLEPFLAPYPKLEAFLRFLSRGTLSSPRFAVDDSRLMGAVESHVQAVLEPGEGQEEARILFLISLLRYLQLAVISGEELPPEGWSVKTTAHIESVMDWIEDHFRQPFSLELLAGELHLSSYYVSHLFKQYTGVSLTDYVTARRIREACVLLGSSGQSVQRIAREVGGLSAPYFCKLFKKHKGMTPLDYRSALHHTAK

Crispr_ID: NZ_LN831776_29

• CRISPR_ID: NZ_LN831776_29
• CRISPR_location: 2204223-2204297
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_29

Consensus_repeat	Method
AATTAGTGTCCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_29

>29.1|2204246|29|NZ_LN831776|CRISPRCasFinder
CATCTGCCCGAGGGTAGGGTACTCCCGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_29

CRISPR arrays

The CRISPR arrays of NZ_LN831776_29

>merge|NZ_LN831776|29|2204223-2204297|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTTCATCTGCCCGAGGGTAGGGTACTCCCGCAAATTAGTGTACCTTTTTCCACTT

>NZ_LN831776|29|31|2204223-2204297|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTT	CATCTGCCCGAGGGTAGGGTACTCCCGCA
AATTAGTGTACCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020432424.1|2198781_2199669_+|ROK-family-protein	unknown	unknown	gnl|CDD|366120
NZ_LN831776.1|WP_020432426.1|2197280_2198777_+|glycoside-hydrolase-family-32-protein	unknown	unknown	gnl|CDD|350134
NZ_LN831776.1|WP_020426318.1|2206863_2207640_+|NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|223528
NZ_LN831776.1|WP_020426315.1|2209738_2211004_-|carbohydrate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|224567
NZ_LN831776.1|WP_020426314.1|2211042_2211882_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_020432430.1|2194694_2195576_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_046501952.1|2208560_2209373_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_039790753.1|2191546_2192107_+|sugar-O-acetyltransferase	unknown	unknown	gnl|CDD|100047
NZ_LN831776.1|WP_046501949.1|2207657_2208437_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224044
NZ_LN831776.1|WP_039785655.1|2211881_2212763_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_020432439.1|2190437_2191469_+|ROK-family-protein	unknown	unknown	gnl|CDD|224851
NZ_LN831776.1|WP_039790754.1|2188629_2189763_+|serine-hydrolase	unknown	unknown	gnl|CDD|365903
NZ_LN831776.1|WP_167345596.1|2213807_2214299_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426319.1|2206147_2206732_+|TetR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|379534
NZ_LN831776.1|WP_020432435.1|2192265_2193312_-|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|380629
NZ_LN831776.1|WP_085979245.1|2193708_2194677_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_LN831776.1|WP_081487091.1|2204417_2205944_-|DHA2-family-efflux-MFS-transporter-permease-subunit	unknown	unknown	gnl|CDD|129794
NZ_LN831776.1|WP_039790751.1|2195629_2197249_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270299
NZ_LN831776.1|WP_020426312.1|2213088_2213769_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_052741432.1|2199993_2203848_+|DUF1080-domain-containing-protein	unknown	unknown	gnl|CDD|350134

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020432424.1|2198781_2199669_+|ROK-family-protein	gnl|CDD|366120	pfam00480, ROK, ROK family.	1.10495e-78
NZ_LN831776.1|WP_020432426.1|2197280_2198777_+|glycoside-hydrolase-family-32-protein	gnl|CDD|350134	cd18622, GH32_Inu-like, glycoside hydrolase family 32 protein such as Aspergillus ficuum endo-inulinase (Inu2). This subfamily of glycosyl hydrolase family GH32 includes endo-inulinase (inu2, EC 3.2.1.7), exo-inulinase (Inu1, EC 3.2.1.80), invertase (EC 3.2.1.26), and levan fructotransferase (LftA, EC 4.2.2.16), among others. These enzymes cleave sucrose into fructose and glucose via beta-fructofuranosidase activity, producing invert sugar that is a mixture of dextrorotatory D-glucose and levorotatory D-fructose, thus named invertase (EC 3.2.1.26). These retaining enzymes (i.e. they retain the configuration at anomeric carbon atom of the substrate) catalyze hydrolysis in two steps involving a covalent glycosyl enzyme intermediate: an aspartate located close to the N-terminus acts as the catalytic nucleophile and a glutamate acts as the general acid/base; a conserved aspartate residue in the Arg-Asp-Pro (RDP) motif stabilizes the transition state. These enzymes are predicted to display a 5-fold beta-propeller fold as found for GH43 and CH68. The breakdown of sucrose is widely used as a carbon or energy source by bacteria, fungi, and plants. Invertase is used commercially in the confectionery industry, since fructose has a sweeter taste than sucrose and a lower tendency to crystallize. A common structural feature of all these enzymes is a 5-bladed beta-propeller domain, similar to GH43, that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	6.064e-161
NZ_LN831776.1|WP_020426318.1|2206863_2207640_+|NAD(P)-dependent-oxidoreductase	gnl|CDD|223528	COG0451, WcaG, Nucleoside-diphosphate-sugar epimerases [Cell envelope biogenesis, outer membrane / Carbohydrate transport and metabolism].	2.71474e-22
NZ_LN831776.1|WP_020426315.1|2209738_2211004_-|carbohydrate-ABC-transporter-substrate-binding-protein	gnl|CDD|224567	COG1653, UgpB, ABC-type sugar transport system, periplasmic component [Carbohydrate transport and metabolism].	2.58021e-51
NZ_LN831776.1|WP_020426314.1|2211042_2211882_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	2.07883e-75
NZ_LN831776.1|WP_020432430.1|2194694_2195576_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	5.45402e-63
NZ_LN831776.1|WP_046501952.1|2208560_2209373_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	3.32476e-24
NZ_LN831776.1|WP_039790753.1|2191546_2192107_+|sugar-O-acetyltransferase	gnl|CDD|100047	cd03357, LbH_MAT_GAT, Maltose O-acetyltransferase (MAT) and Galactoside O-acetyltransferase (GAT): MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively at the C6 position of the nonreducing end glucosyl moiety. GAT specifically acetylates galactopyranosides. Furthermore, MAT shows higher affinity toward artificial substrates containing an alkyl or hydrophobic chain as well as a glucosyl unit. Active MAT and GAT are homotrimers, with each subunit consisting of an N-terminal alpha-helical region and a C-terminal left-handed parallel alpha-helix (LbH) subdomain with 6 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X).	4.33624e-103
NZ_LN831776.1|WP_046501949.1|2207657_2208437_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224044	COG1119, ModF, ABC-type molybdenum transport system, ATPase component/photorepair protein PhrA [Inorganic ion transport and metabolism].	1.85313e-92
NZ_LN831776.1|WP_039785655.1|2211881_2212763_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	3.89297e-69
NZ_LN831776.1|WP_020432439.1|2190437_2191469_+|ROK-family-protein	gnl|CDD|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	4.44044e-15
NZ_LN831776.1|WP_039790754.1|2188629_2189763_+|serine-hydrolase	gnl|CDD|365903	pfam00144, Beta-lactamase, Beta-lactamase. This family appears to be distantly related to pfam00905 and PF00768 D-alanyl-D-alanine carboxypeptidase.	1.21834e-52
NZ_LN831776.1|WP_020426319.1|2206147_2206732_+|TetR-family-transcriptional-regulator	gnl|CDD|379534	pfam14278, TetR_C_8, Transcriptional regulator C-terminal region. This domain is a tetracycline repressor, domain 2, or C-terminus.	4.60005e-18
NZ_LN831776.1|WP_020432435.1|2192265_2193312_-|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|380629	cd19974, PBP1_LacI-like, ligand-binding domain of uncharacterized DNA-binding regulatory proteins that are members of the LacI-GalR family of bacterial transcription repressors. This group includes the ligand-binding domain of uncharacterized DNA-binding regulatory proteins that are members of the LacI-GalR family of bacterial transcription repressors. The LacI-GalR family repressors are composed of two functional domains: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal ligand-binding domain, which is homologous to the sugar-binding domain of ABC-type transport systems that contain the type 1 periplasmic binding protein-like fold. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcription repressor undergoes a conformational change upon ligand binding which in turn changes the DNA binding affinity of the repressor.	3.02963e-90
NZ_LN831776.1|WP_085979245.1|2193708_2194677_+|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	1.62907e-120
NZ_LN831776.1|WP_081487091.1|2204417_2205944_-|DHA2-family-efflux-MFS-transporter-permease-subunit	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	2.0123e-108
NZ_LN831776.1|WP_039790751.1|2195629_2197249_+|extracellular-solute-binding-protein	gnl|CDD|270299	cd13581, PBP2_AlgQ_like_2, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	4.39173e-179
NZ_LN831776.1|WP_052741432.1|2199993_2203848_+|DUF1080-domain-containing-protein	gnl|CDD|350134	cd18622, GH32_Inu-like, glycoside hydrolase family 32 protein such as Aspergillus ficuum endo-inulinase (Inu2). This subfamily of glycosyl hydrolase family GH32 includes endo-inulinase (inu2, EC 3.2.1.7), exo-inulinase (Inu1, EC 3.2.1.80), invertase (EC 3.2.1.26), and levan fructotransferase (LftA, EC 4.2.2.16), among others. These enzymes cleave sucrose into fructose and glucose via beta-fructofuranosidase activity, producing invert sugar that is a mixture of dextrorotatory D-glucose and levorotatory D-fructose, thus named invertase (EC 3.2.1.26). These retaining enzymes (i.e. they retain the configuration at anomeric carbon atom of the substrate) catalyze hydrolysis in two steps involving a covalent glycosyl enzyme intermediate: an aspartate located close to the N-terminus acts as the catalytic nucleophile and a glutamate acts as the general acid/base; a conserved aspartate residue in the Arg-Asp-Pro (RDP) motif stabilizes the transition state. These enzymes are predicted to display a 5-fold beta-propeller fold as found for GH43 and CH68. The breakdown of sucrose is widely used as a carbon or energy source by bacteria, fungi, and plants. Invertase is used commercially in the confectionery industry, since fructose has a sweeter taste than sucrose and a lower tendency to crystallize. A common structural feature of all these enzymes is a 5-bladed beta-propeller domain, similar to GH43, that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	1.92076e-117

Protein sequences

>NZ_LN831776.1|WP_052741432.1|2199993_2203848_+|DUF1080-domain-containing-protein
MKKKFRTVLCFLLVIGTVMASSGLYAVNPATGWAAPADQGTGEPDKEGLAINENAAKVITNLTGWQVKGKGEMKNTAEGLLLTSDPQQNVMAVSETAAEDFLYEADVMLKELKADTSLIFRSDDDGKNSYMLQLAPGSGVIRLKDAAGGAGKLYEERQVSLKEGEIYHLKVKAEGTSLKVYWGNQYKPVIEIQDSTYRSGRLGLHVRDGSALFQNITVSDLKGNLGPVLMNKGQWQPDLRGQKGTSANGSKAQRIYSRQAADLVYEGTISLGSNAAAALAFRSSADGVRGYEAVLAREGDQVGVKLAKADGTVVASSEHLYPSRTGAKHHVEIKAKGSRIQVFLDGYTPAAIDIQDTAYSTGHAGLVVKTGNAYFQETYLTDADSYYNETFRPRYHYSPVRGSASDPNGLVYFEGEYHLFHQDGGTWAHAVSKDMLNWKRLPIALPWNDYGHIWSGAAVADAANASGLFTDSGGKGLIAYYTSYNPDGPNGNQRIGLAYSKDKGRTWEYAKDRPIVIENPGKNGEDPGGWDFRDPKVVRDDGNNRWVMVVSGGDHIRFFTSTNLLDWTLTDNWGYGDYVRGGVWECPDLFPLTVQGTSQKKWVLMISTGANPATGGSDSEYFVGSLTAEGKFVNDNPAGKVLRTDFGKEYYASMSFSDMPDGRRVMLAWMSNWDYPFAFPTSGWKGELTVPREVTLVMTPEGLRLAQSPVKEIEQLRSRLFTAADKRVNSSSPNLLKGLVAGAYEIEAELEIPDGSTATEFGFNVREGADQKTVVGYKVGESQLFVDRSASGVTDFSSLFSTRHEAAMTAENKRIKLRILVDESSVEVFGNGGKAVFSEVIFPDPASRAMSFYSQGGMVKVISLKVNKLGPVWNSDSSAATRIAMDTADRELETGDSVTLQAAVENGPGNGVHPLKWKSSNEEVAGISAADFSQATLQAKKAGEAVITVSTPNGKASASLVVKVYGGEFHTNLSGWTQDLSMASWIATGDGIRGKYSSDANHMAQEQAGNFTYEADMKLGESGGAGSLLFRASGDGRSGYYLNLDPNMKSVRLFYKLDGRFEERQVLAKYPAFILPGQTYNIKIQAEGPRIIVYMGGRQIMDLKDGTFAEGHFGLHVFGGEASFQNVKVTGGAPADLMTSSLVNTASGKSLYTDSLTNGEAVKVRNANEATDQKWVFVPTGDEAGSYSIRTTAGQALDLDTGQNRIQLYSYLGYNNQRWIIQKNEDGSAAIISAHQHLALAISGDGSKLTLEEYRTDEMRQKWRINPDSHGSFKGTEEIRPSAE
>NZ_LN831776.1|WP_020432424.1|2198781_2199669_+|ROK-family-protein
MRIGAIEAGGTKFVLGIGDEKGEILDRLSLPTGHPDQTLPQVIEYFQDKEVEAIGVGSFGPIDINPESPTYGCVTSTPKPGWENYDMLGTLRHAFPVPFGWDTDVNAAAYGEAKWGAAQGLSSCLYYTVGTGVGVGVYSEGTIIHGLVHPEGGHVLTRRHPEDKFAGVCPYHGDCLEGMAAGPAIEARWGKKGHELPLDHAAWEMEAFYIAQSITSAILLLSPHKIILGGGVMQQQQLFPLIRQAVLRNLNGYVRSSSLLDHMDEYIVPPGLGPQAGLYGALALGLAAWKHEAAK
>NZ_LN831776.1|WP_020432426.1|2197280_2198777_+|glycoside-hydrolase-family-32-protein
MPASTKQNYRGVYHFSPQAKWMNDPNGMVYFEGEYHLFFQHHPDGMTMGAMHWGHAVSKDLVTWEELPVALFPDELGMIFSGSAVVDWNNTTGFFADKPGLVAIFTHHLDMPEGQPPVQRQSLAYSHDNGRTWTKYEGNPVLEDDAFIDFRDPKVFWNRETGKWVMIVACGQTVCLYHSPDLIHWTFASEFGKGIGSHDGVWECPDLFPLHVDGDTSNIKWVMLVSIGADPAFAEGSRTQYFTGDFDGNVFTPDEDSRTIRWLDYGRDNYAGVSWSDVPEADGRRLFIGWMSNWMYAQQTPAEEFRGAMTLPRELYLESREGNILLVQKPAQELEAARIPVLSLKDVTVQEVNASLAGLQLDAYEIAAKLPRGMSAGFKVRVGAGEETVTGIDAQTGELYVDRAASGLTGFHERYPGRHSAALQAPGEIHDLHIYVDRTSVEVFGNGGQAVITDLIFPKPESAGIAAFAEHEETPFLSLEVYKLALPAAIGDDRQSEG
>NZ_LN831776.1|WP_039790751.1|2195629_2197249_+|extracellular-solute-binding-protein
MSMKKTTKSKVVTKAASASVLASLMFLSACSGGGGGSAASKEQDPSGKVTLNFITQSSPLAPADPNDKLINKRLEEKTNVHINWKNFTKDVFVEKRNLAVASGDLPDAIFNADYSDYELLKLAKDGTIIPLNDLIEKNMPNFKKVLEEAPEYKSMITAPDGNIYAFPWIEELGNGKERIQAVDSMPWINVEWLKKLGLEMPKTTDELKKVLIAFKTQDPNGNGQADEIPLSFINKPGAEDLAFLFASFGLGENPDHAVVSDDGKVIFTAAEEGYKNAISFINELYKEGLIDIEAYTQDWSTYLAKGKEQRYGLYFSWDKANISGANDAYDVMPPLAGPDGEVNVTRTNGLGLGRGKMVVTSANKNLETTAKWVDQLYDPLQSVQDNWGTYGDETQQNIFELDEAKGMLKHLPLEGAAPVELREKTSIGGPLAVLDSYYGKYTTMPDDAKGRMDIIKNIMAPKMKAENVMPSVFNSIEELDRLTTIETDLFAYVLRMRTEWYQNGKVNEQWGEYLKELDRLGLQEWLKIKQDGYDRATKK
>NZ_LN831776.1|WP_020432430.1|2194694_2195576_+|carbohydrate-ABC-transporter-permease
MFIKHSRLDRFILALNATFLTLAVLVVVLPLVYVVIASFMDPSVLLSHGLSFKISDWSLDGYKMILTNPAMIRGFGNAVFYSVAFAILTVLVSICAGYALSDDRLKGRGFFMTLFIITMFFGGGLVPTYLLVKNLGLLDTVWAVIIPGAVNVWNIILSRTFFKGVPNELREAANVDGASEWRIFIGIVLPLSKPIIFVLALYAFVGQWNSYFDAMIYLDNPNLHPLQLVLRSILIQNQVDPGMISDQLAMAEMKRLSEIIKYAAIVVSSLPLIIMYPFFQKYFEKGVMLGSLK
>NZ_LN831776.1|WP_085979245.1|2193708_2194677_+|sugar-ABC-transporter-permease
MEAKALQNTIKANAGSTVPRSSGSLLNFVKKHYFLYLMLAPALILTLIFKYGPMYGAIIAFKDFSPIKGILGSEWVGFYNFNKFLSSPNFEVIFMNTLKLSFFGLILSFPVPILLALMLNQVRKSAIKKNIQLFLYAPNFISVVVVVGMLFIFLSPTGPINQLLTWATGEPVMFMSRPEYFRWIYILSDIWTSAGWASIIYVAALANVDPELHNAANLDGANLLQRIRHIDLPTIRPIMAIVFILAAGGIMSIGFEKAYLMQTATNLPTSEIIPTYVYKIGLQSGDYAYSAAVGLFNSLINVVLLITVNFIVKKLNEGDGLY
>NZ_LN831776.1|WP_020432435.1|2192265_2193312_-|LacI-family-DNA-binding-transcriptional-regulator
MARDRVTIQDIADALGISRNTASKALNGVDSIPAETRDKVIKKAVELKYKQFSYMETTIGTSEKQGNIALLTCNLPNGSHFGSLLISGLEKEISTKGYTLSIYFVRENDINGMTLPGNFEPSSVDGIICIEMFNKAYSKLITDLGIPTIFIDCAADMVYPELKADLVLMENEHSTYSVTRKLIDHGYTSFGFVGDYNHCKSFNERWTGFNRALTECGITLDPAHNIVAPDRNFNINMEENWMGHQLDALEAWPSVFICANDFIAISVMKSLKNKGIKVPEEVAVCGFDDASESRVVEPHLTTVHIYSSQMGIISAEILLSRIKDNTKPYQVTHVATDMIFRGSTPALN
>NZ_LN831776.1|WP_039790753.1|2191546_2192107_+|sugar-O-acetyltransferase
MKTEKQKMLNGELYMGWDPELTRERAYARRMTRIYNQTTELDDELRVQILKELMGSTGENLGMEPNIRVDYGYNIHVGEHFYANFDCTILDVCEVRIGNNCLFGPGVQVYTATHPVDPSERIKGPEYGKPVTIGNNVWVGGQAIINPGVTIGDNVVIASGAVVTKDVPDNVIVGGNPAKVIKKIDL
>NZ_LN831776.1|WP_020432439.1|2190437_2191469_+|ROK-family-protein
MNPITNNTMRVKKMNKELVRQALKTMKQGTKSMLAQATGLSVATCGNILNELIDTGELLELDMEESSGGRPARLYRYNVNFSYIACIIIRAGVKTHSLTYTVANLAGEAIKEGYQETDRMEPDMIEKLVDQLIGEFPQIRAVGIGVPGAVNQGIINVSDIKELINVPLEASIRDKHGVEVIMDNDMNLTVYGFYQKQGYDEEKSVAVVTFIEGCFPGAGMMVDGHILRGSTRFAGEIAFLPFGMSHEEQFRQLHERTTFYSLAGRAVSSLIAIMNPETIALTGSLVEPADVELIRQECLKYIPEMHMPQLMLLENPHENYMYGLITMTLESLSYSLQLIEKRR
>NZ_LN831776.1|WP_039790754.1|2188629_2189763_+|serine-hydrolase
MNFEPLSSFIDRITSWRIPWAEVLVMHRNEPVYRYRNGYASLEEKTPIDDGRIINLYSLTKIMTCTAALQLLEKGAFLLNDRLSDYLPEYTEMNVKKRLPGGELAFERAVNPITVRDLFTMSAGFSYDLELPSIKEAVSRTGGKMPTRAIAEALAKEPLQFEPGTRWNYSLCHDVLAALVEAVDGRRFGTYIREEITGPLGMTDTGFDLPDGKRSRLAPQYEYSDELGKPVRKDGNGFRLGTEYESGGAGLLSTVTDYAQFLNTLTNLGTSPDGVRILSPASVELMRTEQLTESMRGDFSWEQLKGYSYGLGVRTHISQARSGSLSPLGEFGWSGAAGCLAVIDPASQLTVMYAQHMLNNQEPFVHPRLRNIVYACL
>NZ_LN831776.1|WP_081487091.1|2204417_2205944_-|DHA2-family-efflux-MFS-transporter-permease-subunit
MIGDLKGWSGVSNKTEAISSSVKKGPILFIMILGAFLATLNQTVMSVATPELMHDFNITAATAQWLTTGYMLVNGVLIPITAFLMQRFTTRELFQSSMFIFLAGTVVSALATSFPILLTGRMIQAAGAGIIMPLLTNVILTLFPREKRGAAMGMVGLAIIFAPAIGPTLAGYILEHYSWETMFYGMLPLTAIVIICGFIYLKNVAERSYPKIDLASVILSTVGFGTLLYGFSRAASAGWSSAEVIATLAAGVLSLGLFTWRQLASSSPLLDLRVFKYNMFSLTTIINIAVTIIMYADMMLLPLYLQNARGYTAMESGLLLLPGALVMGLLMPVTGKLFDRFGAKWLAVTGLLITIVTTLSFVNLTDSTNYTYLVLMSTGRRIGMALLLMPIQTLGLNQLPSKLNAHGTAISNTIRQVAGAVGTSLLVTVMTSRTTTHLMDMMAAGGAKGASKEHMIMEASIQGINDAYLVIVGIGIIGLLLAFFIKRVGQASDQEPGAQLKQAIAEKA
>NZ_LN831776.1|WP_020426319.1|2206147_2206732_+|TetR-family-transcriptional-regulator
MNHTTPRTDPRVVRTRELLKDAVVELMEEMNVQKISVNRIAERAKINRVTFYLHYKDIPDMLEKMADEMVEDITRVVNSNAAGNSEPGEHEDWPVLENLLKYIAENARFYKTVLTSRRSSIFSDRLFNLIADMIAARVERGVSAADTSQVSIQKDIATWYGSAALIGTIIAWLRNDMPYTPSYLAKQITSLRSK
>NZ_LN831776.1|WP_020426318.1|2206863_2207640_+|NAD(P)-dependent-oxidoreductase
MKRKLLITGAAGRIGNVIYRGLQEDGRYDVAGADIQADESQGIVQMDVADEARLAELTQGVDTVLHFAWIKDNEDFLGKVLPGNVSGAYKLFEAAVQNGVRRMVFASSNHATGFYKTDEKTEPTDPYRPDSFYGLSKCYIELLGRLYSDQGKISSFNIRIGNFPGDDRPHSERAGHIWISERDMLQLIVCCIEADEGLKYLNLYGTSANSDNYYNIGYLEDLIGYRPQDDATKLLEQAKAAGREVRQDETVYQGGQEL
>NZ_LN831776.1|WP_046501949.1|2207657_2208437_-|ABC-transporter-ATP-binding-protein
MIIDLHDVTWTQGIHTLLNGVNWTVRPGEHWALLGLNGSGKTTLLNMITGYLWPTTGSISVLGERYGEVDLREMRKSIGWVSSSLQEKLYGTDRTQNVVISGKHATIGLYDHLTEQDTVRAGELMKQLGCFHLWDREYRTCSQGEKQKLLIARALMADPRVLILDEPCNGLDLFSRERLLDSIRELALSKEMPTLIYVTHHTEEILPVFSHTLLLRRGQVVQSGLTSEVLTAGVLSDFFESEVIVERHGERVYVRAAQN
>NZ_LN831776.1|WP_046501952.1|2208560_2209373_+|helix-turn-helix-transcriptional-regulator
MEINLLTDTFELWKGKNGFANTPHAHADWYQVTLPVQGTCDLLQNRQTYLLQPGEGLLQHPGTEHSFQVGALSAVIVIKFRGSLLNHKAPGDSQEYRLARDFNPKEITALFRSWSYELLGNETDSLMVQQMEFQVQLYLERLLQGEGESDRPGLQNSVSRPYTSDPHMTRVLDYLHSCYMTAVDIESMAAIALQSRYHFIRSFKQLTQFTPYQYVLRLRINEAGKRLRLSEESVTDISFSLGFSSVTQFYRTFLRLKGMTPTQYRKRTSI
>NZ_LN831776.1|WP_020426315.1|2209738_2211004_-|carbohydrate-ABC-transporter-substrate-binding-protein
MRKIRGLLLACSLLLAALTAGCGRGTDEAGGIKTVHIYQFKVEISEALAKLKTEFEKEHPDIRLEIQSVGGGSDYGASLRAKFSSGDEPDIFTIGGNNERDMWLEYLEDLSGEAWAKDVKPLAAEQMTVNGKLYGMPMNLEGYGFIYNKDLFKQAGITQKPLTLTALREAAEKLKAAGITPFANGYQEWFVLGNHNVNVAFAQQPDPESFIAGLTDGSKHFAGDPVFSKWLDLLDLTVEYGNKNPLSTDYNTQVTMVASGEAAMMQQGNWTQGQIDGIDPDLNLGILPMPIDDTPEDNDKLYVGVPSNWVVNKFSPVKEEAKVFLDWLVTSETGKKYITKEFQFIPALDSIQGTKEDLGALGSEVLEYTDKDQALTWNWSRLPNGMPQELSSNIQGYLGGKLTKEGMLKEFQVNWDNLSVQ
>NZ_LN831776.1|WP_020426314.1|2211042_2211882_-|carbohydrate-ABC-transporter-permease
METTAKKFNVPLLLTELLMILLALVFLVPFYFLLANSVKSYSEILSDSSALPTVFQWNNYAEAWKATDFPHAFLNSLVVTVTSNVLLAFLCSMCAYKMVRNNSRYNRILYVALVAAMVIPFQAIMIPLVQIVSRLGVMDSTAGLILAYLGFGAPMTVFLLHGFVKSVPIDIEEASRVDGSSPYGTFFRVVLPLMQPIIVTVIILNTLWIWNDYLMPSLILQSPALRTIPIATYTFFGQYTKQWDLALPGLVLGITPVVLFFLLMQKYIIEGIAQGSVKG
>NZ_LN831776.1|WP_039785655.1|2211881_2212763_-|sugar-ABC-transporter-permease
MDLKRRSRLMQQFIFVGPTSLFFFVIVLIPFFLGLYYSFTSWNGISRHVGWTGLRNYIHIFTKDPSFLNSFWFTAKFTFFGLVLTNLLGFMLAYVLTRKLFTRNVLRTVFFVPHVIGGLLLGFIWQFIFVRGFASVGQATGWSFFNLPWLGTGATSFWAIVIVFVWQNAGYLMVIYISAINNVPQSLIEASKVDGAGRMQALRHVTIPLVMPAVTVCLFLSISWSFKLFDLNLSLTKGGPFKATESVALNIYNEAYTISRFGMGSAKAMIFFVIVAVISLLQVRATKKREVEL
>NZ_LN831776.1|WP_020426312.1|2213088_2213769_+|hypothetical-protein
MGFAEEHQKWLDSHKKRRTGERLDRLVRGHGHGEKMFVERVWWPIFGHMDDLHPEYEVSDWRGRPYFVDLVWKPGQVKFAIEIKGYGPHVQQTDRTRYRQELNRETYLQIAGYRVVAVPYDDLEAAPELTISLFKSLLAPCMLKNAEGEGRPYTRLESDILRLAARWNGSIRPVDLVNELGVNPRTVKKLMNSLCVKGRFRPILAPGSNRVCRYEYIHSFMEDELW
>NZ_LN831776.1|WP_167345596.1|2213807_2214299_+|hypothetical-protein
MRGENTSDLPATGQRGEMRGKNTSDPPATGQRSRMRGKNTSDLPRIGLGGRMRGKNTSDLPRIGQLSRMRGKNTSDLPRIGQRSKMRGKNTSDPPATGQRGRMRGKNTSDLPRIGQRSKMRGINTSDPSATGLRSRMRGKNTSDLPATGLPPRLDSLFIVQVW

Crispr_ID: NZ_LN831776_30

• CRISPR_ID: NZ_LN831776_30
• CRISPR_location: 2307510-2307586
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_30

Consensus_repeat	Method
TTAGGTGGAAAAAGGTTAACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_30

>30.1|2307535|27|NZ_LN831776|CRISPRCasFinder
TACTCAAGCATCATGCTTCTCCGCAAT

CRISPR arrays and Neighbor proteins around NZ_LN831776_30

CRISPR arrays

The CRISPR arrays of NZ_LN831776_30

>merge|NZ_LN831776|30|2307510-2307586|CRISPRCasFinder
TTAGGTGGAAAAAGGTTAACTAATTTACTCAAGCATCATGCTTCTCCGCAATTTAAGTGGAAAAAGGTTAACTAATT

>NZ_LN831776|30|32|2307510-2307586|CRISPRCasFinder
TTAGGTGGAAAAAGGTTAACTAATT	TACTCAAGCATCATGCTTCTCCGCAAT
TTAAGTGGAAAAAGGTTAACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_046502033.1|2319309_2320935_+|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_046506666.1|2298300_2298759_+|DUF3888-domain-containing-protein	unknown	unknown	gnl|CDD|379024
NZ_LN831776.1|WP_020429622.1|2311374_2312376_+|glycosidase	unknown	unknown	gnl|CDD|350107
NZ_LN831776.1|WP_020429616.1|2321063_2322488_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_LN831776.1|WP_046502018.1|2298987_2299974_+|aminoglycoside-phosphotransferase-family-protein	unknown	unknown	gnl|CDD|366736
NZ_LN831776.1|WP_020429618.1|2317568_2319308_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_020429623.1|2310415_2311252_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_039789361.1|2303891_2305721_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_046502015.1|2295456_2296854_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197775
NZ_LN831776.1|WP_020429624.1|2309499_2310402_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_020429628.1|2302836_2303502_+|SGNH/GDSL-hydrolase-family-protein	unknown	unknown	gnl|CDD|238872
NZ_LN831776.1|WP_052741436.1|2316322_2317348_+|CapA-family-protein	unknown	unknown	gnl|CDD|378215
NZ_LN831776.1|WP_046502024.1|2305707_2307333_+|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_020426871.1|2297179_2297653_+|IS200/IS605-family-transposase	unknown	unknown	gnl|CDD|376616
NZ_LN831776.1|WP_020426871.1|2300223_2300697_+|IS200/IS605-family-transposase	unknown	unknown	gnl|CDD|376616
NZ_LN831776.1|WP_167345599.1|2312408_2315636_+|hypothetical-protein	unknown	unknown	gnl|CDD|375009
NZ_LN831776.1|WP_046502021.1|2301323_2302664_+|erythromycin-esterase-family-protein	unknown	unknown	gnl|CDD|350610
NZ_LN831776.1|WP_046502013.1|2292628_2295307_+|YhgE/Pip-domain-containing-protein	unknown	unknown	gnl|CDD|224428
NZ_LN831776.1|WP_020429615.1|2322559_2323459_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_020429625.1|2307992_2309390_+|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270303

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_046502033.1|2319309_2320935_+|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	9.46328e-50
NZ_LN831776.1|WP_046506666.1|2298300_2298759_+|DUF3888-domain-containing-protein	gnl|CDD|379024	pfam13027, DUF3888, Protein of unknown function (DUF3888). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 111 and 149 amino acids in length.	1.61293e-20
NZ_LN831776.1|WP_020429622.1|2311374_2312376_+|glycosidase	gnl|CDD|350107	cd08993, GH130, Glycosyl hydrolase family 130. This subfamily contains glycosyl hydrolase family 130 (GH130) proteins, as classified by the carbohydrate-active enzymes database (CAZY), are phosphorylases and hydrolases for beta-mannosides, and include beta-1,4-mannosylglucose phosphorylase (EC 2.4.1.281), beta-1,4-mannooligosaccharide phosphorylase (EC 2.4.1.319), among others that have yet to be characterized. They possess 5-bladed beta-propeller domains similar to families 32, 43, 62, 68, 117 (GH32, GH43, GH62, GH68, GH117). GH130 enzymes are involved in the bacterial utilization of mannans or N-linked glycans. Beta-1,4-mannosylglucose phosphorylase is involved in degradation of beta-1,4-D-mannosyl-N-acetyl-D-glucosamine linkages in the core of N-glycans; it produces alpha-mannose 1-phosphate and glucose from 4-O-beta-D-mannosyl-D-glucose and inorganic phosphate, using a critical catalytic Asp as a proton donor. This family includes Ruminococcus albus 4-O-beta-D-mannosyl-D-glucose phosphorylase (RaMP1) and beta-(1,4)-mannooligosaccharide phosphorylase (RaMP2), enzymes that phosphorolyze beta-mannosidic linkages at the non-reducing ends of their substrates, and have substantially diverse substrate specificity that are determined by three loop regions.	2.21929e-143
NZ_LN831776.1|WP_020429616.1|2321063_2322488_+|extracellular-solute-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	3.10035e-50
NZ_LN831776.1|WP_046502018.1|2298987_2299974_+|aminoglycoside-phosphotransferase-family-protein	gnl|CDD|366736	pfam01636, APH, Phosphotransferase enzyme family. This family consists of bacterial antibiotic resistance proteins, which confer resistance to various aminoglycosides they include: aminoglycoside 3'-phosphotransferase or kanamycin kinase / neomycin-kanamycin phosphotransferase and streptomycin 3''-kinase or streptomycin 3''-phosphotransferase. The aminoglycoside phosphotransferases inactivate aminoglycoside antibiotics via phosphorylation. This family also includes homoserine kinase. This family is related to fructosamine kinase pfam03881.	4.31313e-14
NZ_LN831776.1|WP_020429618.1|2317568_2319308_+|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	8.1837e-49
NZ_LN831776.1|WP_020429623.1|2310415_2311252_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	8.86234e-66
NZ_LN831776.1|WP_039789361.1|2303891_2305721_+|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	4.5731e-56
NZ_LN831776.1|WP_046502015.1|2295456_2296854_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|197775	smart00530, HTH_XRE, Helix-turn-helix XRE-family like proteins.	0.000383706
NZ_LN831776.1|WP_020429624.1|2309499_2310402_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.13681e-77
NZ_LN831776.1|WP_020429628.1|2302836_2303502_+|SGNH/GDSL-hydrolase-family-protein	gnl|CDD|238872	cd01834, SGNH_hydrolase_like_2, SGNH_hydrolase subfamily. SGNH hydrolases are a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the Ser-His-Asp(Glu) triad found in other serine hydrolases.	1.05891e-42
NZ_LN831776.1|WP_052741436.1|2316322_2317348_+|CapA-family-protein	gnl|CDD|378215	pfam09587, PGA_cap, Bacterial capsule synthesis protein PGA_cap. This protein is a putative poly-gamma-glutamate capsule biosynthesis protein found in bacteria. Poly-gamma-glutamate is a natural polymer that may be involved in virulence and may help bacteria survive in high salt concentrations. It is a surface-associated protein.	2.14803e-99
NZ_LN831776.1|WP_046502024.1|2305707_2307333_+|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.65757e-51
NZ_LN831776.1|WP_020426871.1|2297179_2297653_+|IS200/IS605-family-transposase	gnl|CDD|376616	pfam01797, Y1_Tnp, Transposase IS200 like. Transposases are needed for efficient transposition of the insertion sequence or transposon DNA. This family includes transposases for IS200 from E. coli.	2.86221e-44
NZ_LN831776.1|WP_020426871.1|2300223_2300697_+|IS200/IS605-family-transposase	gnl|CDD|376616	pfam01797, Y1_Tnp, Transposase IS200 like. Transposases are needed for efficient transposition of the insertion sequence or transposon DNA. This family includes transposases for IS200 from E. coli.	2.86221e-44
NZ_LN831776.1|WP_167345599.1|2312408_2315636_+|hypothetical-protein	gnl|CDD|375009	pfam17132, Glyco_hydro_106, alpha-L-rhamnosidase.	1.48726e-07
NZ_LN831776.1|WP_046502021.1|2301323_2302664_+|erythromycin-esterase-family-protein	gnl|CDD|350610	cd14728, Ere-like, Erythromycin esterase and succinoglycan biosynthesis related proteins. This group contains erythromycin esterase, which shares conserved active site residues of the Tiki/TraB family. Erythromycin esterases (EreA and EreB) disrupt erythromycin via the hydrolysis of the macrolactone ring. A critical catalytic histidine acts as a general base in the activation of a water molecule. Macrolides act by inhibiting bacterial protein synthesis by binding at the exit tunnel of ribosomal subunit 50s, blocking the translation of the polypeptide. Erythromycin esterase, typically found in integrons and transposons, confers antibiotic resistance through the disruption of the drug ring structure. EreB substrate profile is substantially broader than that for EreA, being able to also metabolize semisynthetic derivatives such as azalide azithromycin.	2.53203e-100
NZ_LN831776.1|WP_046502013.1|2292628_2295307_+|YhgE/Pip-domain-containing-protein	gnl|CDD|224428	COG1511, COG1511, Predicted membrane protein [Function unknown].	1.25025e-117
NZ_LN831776.1|WP_020429615.1|2322559_2323459_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	3.88712e-76
NZ_LN831776.1|WP_020429625.1|2307992_2309390_+|sugar-ABC-transporter-substrate-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	2.04019e-53

Protein sequences

>NZ_LN831776.1|WP_046502024.1|2305707_2307333_+|response-regulator
MEYPEVKPVKICVIDDIKSVVDMITRKPQWQEYGIEVAGTALDGEEGLQMVREMKPDIVLTDIRMPRMDGLEMTRAILEFAPHCKIIILSAYSEFSYAQQAIRLGAMDFVKKPFSLEEIVNVVLKAKALCLQEREEQEKIMAMQAQIKESLPILRQEYLTFLMQHRTTEPSAKARWEYLGIPLAQKNFTVFIVEIDHFAEKYGRQPVQEIELIRFSLQNILEETIHAWTQGVIFREATNRYVCIINGGDPHAAGLITEACCANVSRYSRCTVSIGVGLCVAAIHELADSYAQALSALAYHFYTGGNAVYSYASIVHKPRAASHYSVTAEQEFLFALRSGNREKSRLVLQQIFDELLQLDPLPAPQYVENIGYELSFKICRVMLELFPYEKVQPLEQQVNQLKNRLHPSLQEIRSLLEGLCAEACRWIEEERSVESTRIIQQAKAYICANLHTSLTLEQVAKQISLSQGYFSNLFKKVSGISFQQFVMHEKMEKAKTMLIEGMQVQEIAMELGYEHRRYFSEVFKKYTDMTPSEFKISYLGR
>NZ_LN831776.1|WP_039789361.1|2303891_2305721_+|sensor-histidine-kinase
MKLLRQWGGLIWSKWSERFYQVSIKQRVLISFIVLITLSISAMGVLTYRIAGKEIQNNAFDTSKETVDKTLQLLDYRLNDVAMSVQSLMLSDAYRQMMIDVQAHDVTNYYVHLSEMQYVLSQATFNEPMIENVLIATPIGDFYSTTQVRAQDNSFYGSELYDNSKKSPGGYWAKGHYDRLFTGSQRVVSFVVRGIYENTPITNVFIVVNLRENKIASLLGQGTSGNDRKYLLLNTEGETVVQTGWPAKGEPPKDPEFLQDSTADSEGNFFYPFEGENYLVNYKQSAVAPNWILAGMQSKDQVLGQLKGVQRAVLYVILVFLLTTWFFSNKLTAALLRPLFKLSRLMRRVEENQLSVSFESKYNDEIAQVGFQFNRMMTEIKTLIEDVRQKEKDKRHAEIRALTAQMEPHFLYNTLNTIYCKSVMGENDDVNEMILALSQMFQLGLGGGQDLITLEDELSHVQQYCAIQQKCYENLFEYHAEAEEEELLSFPIPKILLQPLVENSIQHGFSDRRSGGCIQVRISLEQSMLHIVVEDNGKGMDAAKVEQGMAKREISKKGYALVNIRHRLQLYYGDEARMELSGQAGVGSRTDLWIPLSPLREEGGNYGIS
>NZ_LN831776.1|WP_020429628.1|2302836_2303502_+|SGNH/GDSL-hydrolase-family-protein
MSTFSGKSKVFLFQGDSITDGNRGRDEDPNHILGHSYAYIIGGRLGNELAEQKPVFYNRGISGDRISDLYARWNEDAIYLKPDVLSILIGVNDLWRIMKGEPSGVTDRFERAYRHVLVETREVLPQTKLVLCEPFILRTGAPAEAWDEWSKHMAHYQQVVRALAEEFGALHVPLQAAFDAAASRADAAYWLWDGVHPTHAGHDLIANEWLSAAGKSGILHG
>NZ_LN831776.1|WP_046502021.1|2301323_2302664_+|erythromycin-esterase-family-protein
MKKKMGIAIAASIITLTSFTGGTYASSKAEVSVTAPYNTNQIAEQIKWLEEHAMPLKTTDPTASLQDLSPLKNMIGSATIVGLGEATHGAHEVFTMKHRIVNYLVHEMGFKALVLEEGWDRALELDRYVLTGKGDPSQYLNPVFNTKEIVDLLQWIRQYNADPKHKSKIRIIGMDIQNVNESVYNNILVYVKKYDSKLATRFEQKMKGLIPVTKDLDTFGGLKKEKKEQYISDAKQIGALLEQNKSKLNGKSPEFAWIKQNARIIEQFTTMVAAYPDNLKDFYLKHDIAMYENAKWTEEHVGKTIVWGHNGHVSKTNMIPFVYPKVAGQYLAEHYGKRYVSIGTSVYEGRYNVYNSKQEFGPFGTLKLDDPSSFNYSFGQVHYDQFFVDLRKASGVTKTWLNEQHPIFAGITTVGPDIPTTIDLSLGKTFDIIVQIQKVNPSQLNR
>NZ_LN831776.1|WP_020426871.1|2300223_2300697_+|IS200/IS605-family-transposase
MANKSYSLAHTKWMCKYHIVFTPKYRRKEIYNQVRKDLIEIFKRLCKYKGVDIIEGHMMPDHVHMLVAIPPKISVSSFMGYLKGKSSLMIFEKHASLKYKYGNRKFWAEGYYVSTVGLNEATVAKYIREQEAHDQAIDKLSVKEYEDPFSRNSSKKK
>NZ_LN831776.1|WP_046502018.1|2298987_2299974_+|aminoglycoside-phosphotransferase-family-protein
MKDSARLFDFQAVNEDMVRRLFSAFDPKASITQVSPLTKGMSTSNYALRTDSGSRYVLRIYPANNDHSGIEAAAYQYAKTKIRTPEIFFFDDSKQIISFSYLIMVFIEGSTLGDFIAENEGCPDHVVHRIGSSLALLHQTKYSHMALLDEHLQIAGQLESFASQYYTLLNGLAGTHIQPSTKEKCMQFLADHAELVERIADKHVFSHGDFIFSNIMVTPSLEPCFIDYEYCFAAPVFYDIGKFFRTRTQVERYIGADTIAAFEEGYNRNAREPLPGEWYALSKLADISTMLHLINKSQIPDGWGSAINGEIEKNLKLLAGEAEPLLDK
>NZ_LN831776.1|WP_046506666.1|2298300_2298759_+|DUF3888-domain-containing-protein
MIRVIIAVVLTVTLSLSSPLQSNAEASYRVPQEDSEELRLQDMLLNFLTPYINDAVRDYYRRLLVEPPLVYPYFVNVVDSMRINEFRGFNLSITLDVTPVVGPHISVGEDRLTFQISVGPEVKLVNYIHLKSYELPPHWQNIVKNMLTGNKS
>NZ_LN831776.1|WP_020426871.1|2297179_2297653_+|IS200/IS605-family-transposase
MANKSYSLAHTKWMCKYHIVFTPKYRRKEIYNQVRKDLIEIFKRLCKYKGVDIIEGHMMPDHVHMLVAIPPKISVSSFMGYLKGKSSLMIFEKHASLKYKYGNRKFWAEGYYVSTVGLNEATVAKYIREQEAHDQAIDKLSVKEYEDPFSRNSSKKK
>NZ_LN831776.1|WP_046502015.1|2295456_2296854_+|helix-turn-helix-transcriptional-regulator
MQFKNTIQAKLDAYLKREGITINQFAGISGVNSGTLSSIINGNRPVAVKQLDRITAGMGLPEGEWYELYIDEYVVNSTPDWRRLGPFLQRCAELDKLECIRQVVRTIMDNISYAQAVFEMGEEWFGQGKRQAAALLYEGVAESEKYQHSERLALCQYRLFKIALGQDQEANLRAAMHFEYFVERLDEADQLNALKDLANIYASLHRWDTVDSLAEKMGHKASIQYHNKYHKVSRRAAQKETARPLCFYILYSHLLRSAVCAEHGDYGQALHYVSRYSDFSWVQERTEEARQIMEQFREWAEANTYLYRLMSGETAVLAGYVDFISTRENEIIPGLTKIMQAANRFGLNVDSIIERFEPHAGLKEQRTLMGKRNMQVTEDQYAVLLFELSVYYLKTQRVHRGLAYLLQNLDLSVRMNSDSAIVGCVALFEQYRHLSSVEDRERYKILIGEVQKTDEKKSGSAAGNR
>NZ_LN831776.1|WP_046502013.1|2292628_2295307_+|YhgE/Pip-domain-containing-protein
MAAVWRIYKKDWLGLFKAPVALLLIAALALLPSVYDWVNVAAVWDPYSNTSGIPIAVASVDQGASVGGKSFNIGDEVLESLRSNKSLGWRFTDVKSAERGVQRGDYYASIVIPAEFSQRMAGVLEGELVKPEVDYTVNEKINAIAPKITAKGASTITAQISERFTETLSSTVLTALSAIDREFQAELPVIRKVEQGLFQLEAGLPEIEQAGRLVLKLQQDWPQLADSAGRIAALADKLPEVEQAGKAAELLDEHWGQISDAAGRLQELQGRLPDLARAKELLSGLDADFSRVGEVLDRASDRLEEAGKVVAAAARALPQTDRIAAAGPAFGQELLQYLAQNRAAFTAVPQVLQQNLHLLQQNADSAALLASQLAEGTAPPDAAAASRLQLAADRLTAGSGALQHTAALFAAVNTLAPGTVPGSELRALTGARASWAAGAAQAARLAAGLRDGGGLDPAALAQLGGDSAKGAAALGGILARYSAEGQSALQGTLQQLTSVAGTAATALQQAPQRLAALSAVLDEAGTAIQYGQTGLAALRDKLPAAAGEVSAAAAGISGRLAAFTGFVTDVLPRIQNGLPAAGEHIHAAAEFARKDLPGAEEKFRRASEWITAGLPRADRGVNRAAELVRNDLPALEHAVRRAADTVRKVKREVNLEEIAQLLGGDIKGTSDFLASPVVLKEKALYPIPNYGSAMTPFYVVLSLWVGGTLLISLLRIGVDTGGIPYRRHQLYFGRLLTFLTVGIFQALIAVLGNMYLLKCYVADKLWFVLFAVLISIVFVTIVFTLVYVFGNLGKGIAIVFMVLQFSSSGGTFPISTTGRFFQILNPFMPFTYAISLLREAVGGILPEVAVRDALYLVLFGMLALVLALTLQKPLERFIRRAAEQAEASRLIS
>NZ_LN831776.1|WP_020429625.1|2307992_2309390_+|sugar-ABC-transporter-substrate-binding-protein
MKKQLLLTSLSAVLAFGLAACGNSNTAENSGEASNAGKTSDAGAASGEKTKITYWTGDRHDAEFVKEKVAEFNKTNTDGIEVELVVKGDDFDTALDLSFQTSDSPDVIRVKENTIGTFYKKEYLAPIDEYLSDDMKAKFPEMTDLNIFDGKRYSLPNYGTTMRLIYNKDLFAKAGVTNPPTTLQELVDTAKKLTAAGKADGAYGFAQNFKSPASAFGRSARVIAEMSGFGGFGYDFKTARFDFSGFKPIIEAFKQIRDDGSMLPGVESLDIDPLRAQFAEGKIGMYLSYSSEPGVYSTQFPAKIDWAAAPAPTIDGKVKGASGFLGGQWLALSSKSKHKDAAWKFMEYMYSDQMLTTYQEKGFGISMVPSISAAAKTPEVNGIEGFLPNQYDGVWPVYPSVAPEGMKSDDAFFKYMLNGGDLDATISDLNKRYNAALDDAIKNDGLKAEPDPSFDPAALAGKFAK
>NZ_LN831776.1|WP_020429624.1|2309499_2310402_+|sugar-ABC-transporter-permease
MNKSKNAAFAYSFLLPSALLTLVLGIYPIAWAFRYMFYNYKGYGTARFIGLDNFSRILRDTEFWNSVVNTFVYAGGKLLLSIPLSLLLAAILNRKIRGRQLLRAVFFMPTVISTAVMAVVFFTIFNSYNGILNQFLIKFNISSSGIDWLGPKHAMLTVILVAVWGAVGNYMLLFLAGLQNIPEDVYESSSLDGANKIQQFRFITLPMLGPVLQMVIMLAIINALKGYESIMVLTEGGPAGKTEVMFLYLYKLFFPVGGSAASTQVQEFGYGSAVAFVSAVIVGMISLIYFYASRRMNRID
>NZ_LN831776.1|WP_020429623.1|2310415_2311252_+|carbohydrate-ABC-transporter-permease
MRTKEITGKTVLWIFLLAFAFITLIPVVITILGSFKTNSELTTGATFLPSKWHFSNYAEAWDQANFSTYTVNSLIVSLSTVAGTLLVASMAAYVVDRMDFFGKKIYVGIQSFTMFVAVGAVVLRPQFDLMVKLHLHSSLWGVILILISAHASIFFILLSFMRGIPRELDEAARIDGSSLGRTFWTIILPLLGPGLGVGALFTFRGAWNEYLLPLVFTMTKPELQTLTVGLANLKYGISAASQTHYMMAGACLSILPILIAYVFANKSFMQMTAGSLKG
>NZ_LN831776.1|WP_020429622.1|2311374_2312376_+|glycosidase
MTVQVPAILTSSPVIHRYEGNPVLDASKVPYNTALVFNAGVTKFKGKYVMVFRNDYGSLADQTIEPHHTTDLGIAFSDDGIHWEASPKKCFKLHDEEIIRAYDPRLTVIGDRCYMCFAVDTRHGIRGGIAVTDDFEEFEILSLSSPDLRNMVLFPEKIGGNYVRLERPFTVYSRGGKDRFDTWISESPDLKYWGNSDLLLAVEHVPFANDKVGPAAPPVKTDKGWLTTFHAVDIDPSRGKHGWEPAWKKRYTAGIMLLDLDNPKKILGMYKQPLLAPETSYEIDGGFRNNVIFPGGMILEDNGEVKIYYGSADTIECLATAHVDDLVSLCLKG
>NZ_LN831776.1|WP_167345599.1|2312408_2315636_+|hypothetical-protein
MTNRETNRILNPWDTLKNPPAAYRSVPLWSWNDLLEKEELERQIEEMHRAGIGGFFMHARGGLQTPYMGEEWMEAIRTSIEKSRELGMNAWFYDENGWPSGFADGKVPAKGLDYQQKRLVCEQAPFEDVPAERIIGWYAAGPDGGADYRLLPPGEEARADLRISYDVNPYYTDTLSSMAVKEFIDSTYERYWKQFGEKYGGELSGIFTDEPQFGRGALPWSFELEDMFIRRHGGNVKEVLPALFLDTMGASRARYAYWETVTFMFTQAYAKQIGDWCAGKGWSATGHVVDEQELMHQVTSVGDPMAFYEHLQIPGCDWLGRFVGNDAMVPKQVSSVARQLGKKRAITESFGCSGWNVSFADLKRIGEWQFVHGINLLCQHLQGYSLRGLRKRDYPPSLFYQQPWWSEYKNFNDYFARLSLLLSEGAAQAEVLLLHPVRTAWTLQRGGDYSAVIPYHEAFARLTRWLCQSLIEHDYGSEGIIAGHGRVSGGSFIVGEAAYRVVIVPPSVTVDRRTAELLREFSAQGGTLIAFEPYPVLVDGQEDAEFARFMEAAVLPEWSCEALCRAVSAGAGPSLQISGGNGEPVAADTLNVRTLELAGSILHYVVNSGTEFYPLLNIQLTRQGTVSLVDLETGEIRPLEQKLLGRDLMELEPLERDQMEQELLEQELPEQEQVQAGQKQMGQKLQPQGVRLQLPLHPGQSYMLKVDPFTGSAPITGDYGSVREQSDNQERSPVELAADWEIVHADLNSLTLDNARLRVDGGEWSELQPVIFIQEQLLAYGRTVTAELEFAFAVGFDTARQRELYLVIERPEELEVELNGARVETAGSGWWRDISFRTIDISGLAAAGRNTLVLRMEFHSSQEIADRLARAKAFEAEGNKLTIDQELESIYLLGDFGVHSGSGFTDGERRAVCTEGPFQLMEPARQVQTGDLTRQGFPFFSGSLRLRQTLELDAARASGAQWFFQSPPDAIVTKLFINGAEVRSFLWEPYDADISSFLHSGSNVIELELTGSCRNLLGPHHHIKGEVYKVGPDSYKDKPGWTDKDLDKDTHVYQTRYAFVKFGLAASPLIYVEQA
>NZ_LN831776.1|WP_052741436.1|2316322_2317348_+|CapA-family-protein
MTEIQIAAVGDLMVKRYIISEARRSDGTHSFDALFAKVAPYLKQADLTIGNLETTFAGNGPNSRRTLRSSGPIFKCPDELAPALKKAGFDVLVTANNHCMDYGTPGLIRTLQVLDRNGISHTGTSRSLEESKQVLIKNVKGIKIGILSYTAGTNRIPVPANRPWLVNRIETGKISREIRKLKKKVDLVLLYLHFGNEYHYTPNKRQKQLVNLFFKHGANIILGSHPHVLQPMESRGKKKFVIYSLGNFVSTKLMNIPYTQSGIILNLTIQKDQKGNTNITNVNYIPTGVDRRMASGSTMTEVVPIRDALKTGVPDRTGRRNHLNRMLNHTESILKREKRRH
>NZ_LN831776.1|WP_020429618.1|2317568_2319308_+|sensor-histidine-kinase
MDYLRRQSFRSKLKIAFLAVILLSVLMTGGLSYYISAATLEKNALKLTQDTVVRSAQIVDEKLNKLMLIMMTFMISQPFHDMLKDAAAGDTSRYYTHLNDLDNVFSQARIAEPLIQSIYVSTPIGEFYPSSMNRNRLTSFKDTFLYGRIEQEQKNIWVEGHEDMLFSGKDRVISLILEPIFDTPVSGVYIVVNIREDGFRKLVQGDTGAGAASFLLNAEGKTVYPVKEPLVRQAVDGGNLSGMMKSPEGNQSFDLDGKTYLLNYAHLGIADWTMTTIQSQASVLKDMVYVKWLIGAVALAAFTVTTLISGAFTGYLLVPLQGLMKVMKRVESNDLSARFESGSGDELAQVGFRFNRMLEQIVVLIGEVTEAETHKRSAEIKALSAQMDPHFLYNTLNTIYWKLNLKQVEPSQKMVLSLSRLFQLGLNKGQEITTLSKELEHVRQYLELQSSCYEGLFHYEIHVREPELAALSIPRIILQPLVENSILHGFRDLESGGRIEIEIAGDGERWVLAVRDNGSGMEEDQVRALFWQESEKGYAVSNLIRRLQLYYGDSAEFYVDSAAGRGTEVRISVPKKGEH
>NZ_LN831776.1|WP_046502033.1|2319309_2320935_+|response-regulator
MYNHETVSLCIIDDIKSVVDGLTAMSWEDQGIQVAGVSGNGEEGLKLITEVRPDLVITDIRMPRMDGLSMLRAVLEDNRSCKVILISGYADFEYAQQAVQLGAFDFVVKPFSEEDIMAAVLRAKAEILEERSRRLSLREMEIKLRESMPVLRQEYFTLLVSHRTSWEQAAGRWEFLNIELNPRGFVVMLIEIDRFQEQVAELSIREVELIRFSLLNITQETIAEYAGCAVFRARHNRYLAVMNDTGPVSPIEIAEQCCRNIERYTKFTVSVGVGGRVEETSELPDSYRQAHRALAHHLFTEGNAAIMYDDLHQTGSQEPLALEYKDELLLALRSGNAGRADAILSAIAETLHPLISRQNPDYLLSLYDELAASAIRTFYELVPYRDIQPLIQKFRAVQGTAGLPLASLQRQLLALCTEGAGLVRQNSLSEGQKVIYEAIDYIKSRLPEDITVGECAAHVHLSASYFSSLFKKVTGMTVTQFTTSERIQKAKALLVEGAQVQEVASAVGYEERRYFSEMFKKITGQTPTEFRAGYHPDQPER
>NZ_LN831776.1|WP_020429616.1|2321063_2322488_+|extracellular-solute-binding-protein
MQKKWLGLSLSLMLAAGIAGCGGNGNNSGNSGAANGAAGGSTASPSAEAGGNTAKSGPVQLKYWTDDRHDQEYIKELINKFNETNSDNIQVELTVMSENYTQSVDIAFSSNQAPDVLRLKSANTSEFVKKGYLAPVDSYLTDDMKTKFSSLMLDNVNRFDGKLYSLPNTGLTMRLVYNKDIFAKAGIQNPPVSLQEMVDDAKKITEAGKSEGIYGFALNFKNPKQAFDRSIREILSLSGYQGLGFDLKTGQFDFAPYSQVIEYFKQMYKDGSVLPGAETLDIDPLRAQFAAGKIGMYLSFSTEPGVYKDQFPTEINWAGALAPTLDGQIKGTSEIVSAGTWLGISAKSANQDAAWKFMQYMYGDEVLKTYHEKGFGIAVVPSIVEQAKNPDIKGMEGFLVGEHDSLWPATPSVTPEGSNYADAFFKYILTGGDAKAITEDLNTRYNAALSKAVEKGEVKVTPDPAFDPTKPQGE
>NZ_LN831776.1|WP_020429615.1|2322559_2323459_+|sugar-ABC-transporter-permease
MSIKWKRLGENSLFLIPSIILTVALGIYPLFWMLRYMFYDYAGYGDALFVGLDNFRRLMRDSLFWESVGNTFIFAGGKLLLTLPLSLLLAVILNGRLRGGNLLRGIYFMPTVISTAVISVVFYNIFNSYNGMVNTVLMKLHLVSQPVDWLGPKHAMLTVILVAVWGAVGNYMLLFLAGLQSIPQDLYESAAIDGANAGRRFWNITLPMLAPVAQMVIMLAIIASLKGYESIMVITEGGPIGKTEVMYLYLYKLLFPVSTGSPVAQQLGYGSAVGFASAVIVGAITGLYFFLSRKMNKVY

Crispr_ID: NZ_LN831776_31

• CRISPR_ID: NZ_LN831776_31
• CRISPR_location: 2507447-2507520
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_31

Consensus_repeat	Method
AATTAGTGATCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_31

>31.1|2507470|28|NZ_LN831776|CRISPRCasFinder
AAGCTGCGGAGATCGGTGTGCTGGGGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_31

CRISPR arrays

The CRISPR arrays of NZ_LN831776_31

>merge|NZ_LN831776|31|2507447-2507520|CRISPRCasFinder
AATTAGTGATCCTTTTTCCACTTAAGCTGCGGAGATCGGTGTGCTGGGGCAAATTAGTGATCCTTTTTCCGCTT

>NZ_LN831776|31|33|2507447-2507520|CRISPRCasFinder
AATTAGTGATCCTTTTTCCACTT	AAGCTGCGGAGATCGGTGTGCTGGGGCA
AATTAGTGATCCTTTTTCCGCTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020432752.1|2502305_2504753_+|phenylalanine--tRNA-ligase-subunit-beta	unknown	unknown	gnl|CDD|234804
NZ_LN831776.1|WP_046502162.1|2510052_2512419_+|endonuclease-MutS2	unknown	unknown	gnl|CDD|234750
NZ_LN831776.1|WP_020432739.1|2512450_2512870_+|DUF350-domain-containing-protein	unknown	unknown	gnl|CDD|226289
NZ_LN831776.1|WP_046502156.1|2493645_2495358_+|phosphoenolpyruvate--protein-phosphotransferase	unknown	unknown	gnl|CDD|224006
NZ_LN831776.1|WP_052741438.1|2498289_2499894_-|diguanylate-cyclase	unknown	unknown	gnl|CDD|143635
NZ_LN831776.1|WP_020432774.1|2491214_2493278_+|PTS-transporter-subunit-EIIC	unknown	unknown	gnl|CDD|273923
NZ_LN831776.1|WP_046502153.1|2490021_2490891_+|PRD-domain-containing-protein	unknown	unknown	gnl|CDD|170086
NZ_LN831776.1|WP_046502169.1|2513616_2514831_+|MFS-transporter	unknown	unknown	gnl|CDD|349949
NZ_LN831776.1|WP_020432733.1|2517890_2519423_+|flavocytochrome-c	unknown	unknown	gnl|CDD|180584
NZ_LN831776.1|WP_167345604.1|2488260_2489886_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020432735.1|2514863_2516474_+|two-component-system-sensor-histidine-kinase-DcuS	unknown	unknown	gnl|CDD|236839
NZ_LN831776.1|WP_020432734.1|2516463_2517180_+|response-regulator	unknown	unknown	gnl|CDD|226931
NZ_LN831776.1|WP_020432757.1|2500930_2501965_+|phenylalanine--tRNA-ligase-subunit-alpha	unknown	unknown	gnl|CDD|234780
NZ_LN831776.1|WP_046502166.1|2513000_2513546_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020432771.1|2495754_2498151_+|type-I-pullulanase	unknown	unknown	gnl|CDD|273975
NZ_LN831776.1|WP_020432741.1|2509551_2509899_-|phage-holin-family-protein	unknown	unknown	gnl|CDD|377198
NZ_LN831776.1|WP_020432745.1|2504947_2507119_+|hypothetical-protein	unknown	unknown	gnl|CDD|274008
NZ_LN831776.1|WP_039790804.1|2493377_2493653_+|HPr-family-phosphocarrier-protein	unknown	unknown	gnl|CDD|237503
NZ_LN831776.1|WP_052741439.1|2508385_2509471_+|GGDEF-domain-containing-protein	unknown	unknown	gnl|CDD|143635
NZ_LN831776.1|WP_020432744.1|2507732_2508125_-|hypothetical-protein	unknown	unknown	gnl|CDD|224537

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020432752.1|2502305_2504753_+|phenylalanine--tRNA-ligase-subunit-beta	gnl|CDD|234804	PRK00629, pheT, phenylalanyl-tRNA synthetase subunit beta; Reviewed.	0
NZ_LN831776.1|WP_046502162.1|2510052_2512419_+|endonuclease-MutS2	gnl|CDD|234750	PRK00409, PRK00409, recombination and DNA strand exchange inhibitor protein; Reviewed.	0
NZ_LN831776.1|WP_020432739.1|2512450_2512870_+|DUF350-domain-containing-protein	gnl|CDD|226289	COG3766, COG3766, Predicted membrane protein [Function unknown].	1.28496e-31
NZ_LN831776.1|WP_046502156.1|2493645_2495358_+|phosphoenolpyruvate--protein-phosphotransferase	gnl|CDD|224006	COG1080, PtsA, Phosphoenolpyruvate-protein kinase (PTS system EI component in bacteria) [Carbohydrate transport and metabolism].	0
NZ_LN831776.1|WP_052741438.1|2498289_2499894_-|diguanylate-cyclase	gnl|CDD|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	2.80711e-51
NZ_LN831776.1|WP_020432774.1|2491214_2493278_+|PTS-transporter-subunit-EIIC	gnl|CDD|273923	TIGR02002, PTS_system_glucose-specific_IIABC_component, PTS system, glucose-specific IIBC component. This model represents the combined B and C domains of the PTS transport system enzyme II specific for glucose transport. Many of the genes in this family also include an A domain as part of the same polypeptide and thus should be given the name "PTS system, glucose-specific IIABC component" while the B. subtilus enzyme also contains an enzyme III domain which appears to act independently of the enzyme II domains. This family is most closely related to the N-acetylglucosamine-specific PTS enzymes (TIGR01998). [Transport and binding proteins, Carbohydrates, organic alcohols, and acids].	0
NZ_LN831776.1|WP_046502153.1|2490021_2490891_+|PRD-domain-containing-protein	gnl|CDD|170086	PRK09772, PRK09772, transcriptional antiterminator BglG; Provisional.	1.45171e-46
NZ_LN831776.1|WP_046502169.1|2513616_2514831_+|MFS-transporter	gnl|CDD|349949	cd06174, MFS, Major Facilitator Superfamily. The Major Facilitator Superfamily (MFS) is a large and diverse group of secondary transporters that includes uniporters, symporters, and antiporters. MFS proteins facilitate the transport across cytoplasmic or internal membranes of a variety of substrates including ions, sugar phosphates, drugs, neurotransmitters, nucleosides, amino acids, and peptides. They do so using the electrochemical potential of the transported substrates. Uniporters transport a single substrate, while symporters and antiporters transport two substrates in the same or in opposite directions, respectively, across membranes. MFS proteins are typically 400 to 600 amino acids in length, and the majority contain 12 transmembrane alpha helices (TMs) connected by hydrophilic loops. The N- and C-terminal halves of these proteins display weak similarity and may be the result of a gene duplication/fusion event. Based on kinetic studies and the structures of a few bacterial superfamily members, GlpT (glycerol-3-phosphate transporter), LacY (lactose permease), and EmrD (multidrug transporter), MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement. Bacterial members function primarily for nutrient uptake, and as drug-efflux pumps to confer antibiotic resistance. Some MFS proteins have medical significance in humans such as the glucose transporter Glut4, which is impaired in type II diabetes, and glucose-6-phosphate transporter (G6PT), which causes glycogen storage disease when mutated.	2.82684e-08
NZ_LN831776.1|WP_020432733.1|2517890_2519423_+|flavocytochrome-c	gnl|CDD|180584	PRK06481, PRK06481, flavocytochrome c.	0
NZ_LN831776.1|WP_020432771.1|2495754_2498151_+|type-I-pullulanase	gnl|CDD|273975	TIGR02104, pulA_typeI, pullulanase, type I. Pullulan is an unusual, industrially important polysaccharide in which short alpha-1,4 chains (maltotriose) are connected in alpha-1,6 linkages. Enzymes that cleave alpha-1,6 linkages in pullulan and release maltotriose are called pullulanases although pullulan itself may not be the natural substrate. This family consists of pullulanases related to the subfamilies described in TIGR02102 and TIGR02103 but having a different domain architecture with shorter sequences. Members are called type I pullulanases.	0
NZ_LN831776.1|WP_020432735.1|2514863_2516474_+|two-component-system-sensor-histidine-kinase-DcuS	gnl|CDD|236839	PRK11086, PRK11086, sensory histidine kinase DcuS; Provisional.	0
NZ_LN831776.1|WP_020432734.1|2516463_2517180_+|response-regulator	gnl|CDD|226931	COG4565, CitB, Response regulator of citrate/malate metabolism [Transcription / Signal transduction mechanisms].	2.28421e-82
NZ_LN831776.1|WP_020432757.1|2500930_2501965_+|phenylalanine--tRNA-ligase-subunit-alpha	gnl|CDD|234780	PRK00488, pheS, phenylalanyl-tRNA synthetase subunit alpha; Validated.	0
NZ_LN831776.1|WP_020432744.1|2507732_2508125_-|hypothetical-protein	gnl|CDD|224537	COG1622, CyoA, Heme/copper-type cytochrome/quinol oxidases, subunit 2 [Energy production and conversion].	1.08378e-11
NZ_LN831776.1|WP_020432741.1|2509551_2509899_-|phage-holin-family-protein	gnl|CDD|377198	pfam04020, Phage_holin_4_2, Mycobacterial 4 TMS phage holin, superfamily IV. These proteins are predicted transmembrane proteins with probably four transmembrane spans. The 1.E.40 is represented by the mycobacterial 4 phage holin, but it also contains many cyanobacterial. proteobacterial and firmicute proteins. Holins are encoded within the genomes of Gram-positive and Gram-negative bacteria as well as in those of the bacteriophage of these organisms. The primary function of holins appears to be transport of murein hydrolases across the cytoplasmic membrane to the cell wall where these enzymes hydrolyze the cell wall polymer as a prelude to cell lysis. When chromosomally encoded the enzymes are therefore autolysins. Holins may also facilitate leakage of electrolytes and nutrients from the cell cytoplasm, thereby promoting cell death. Some may catalyze export of nucleases.	1.18695e-11
NZ_LN831776.1|WP_020432745.1|2504947_2507119_+|hypothetical-protein	gnl|CDD|274008	TIGR02168, Chromosome_partition_protein_Smc, chromosome segregation protein SMC, common bacterial type. SMC (structural maintenance of chromosomes) proteins bind DNA and act in organizing and segregating chromosomes for partition. SMC proteins are found in bacteria, archaea, and eukaryotes. This family represents the SMC protein of most bacteria. The smc gene is often associated with scpB (TIGR00281) and scpA genes, where scp stands for segregation and condensation protein. SMC was shown (in Caulobacter crescentus) to be induced early in S phase but present and bound to DNA throughout the cell cycle. [Cellular processes, Cell division, DNA metabolism, Chromosome-associated proteins].	1.42606e-14
NZ_LN831776.1|WP_039790804.1|2493377_2493653_+|HPr-family-phosphocarrier-protein	gnl|CDD|237503	PRK13780, PRK13780, phosphocarrier protein HPr; Provisional.	3.2335e-29
NZ_LN831776.1|WP_052741439.1|2508385_2509471_+|GGDEF-domain-containing-protein	gnl|CDD|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	3.26378e-53

Protein sequences

>NZ_LN831776.1|WP_020432745.1|2504947_2507119_+|hypothetical-protein
MAMDRTRVAVEIYGTSYKLVGSSTEYMKQVARYVDEHMRAISKSHTRLDTPRIAVLAAVHMAEQAIQVQDFKNELNMLTGERTELRVEVARLTEAQKERQEEYERLEAAAREEAARLAAEAEEERRRHLEIQEQERKLHAEALLEAETAAAAAREQLAEELKAREAELKSLRERYEQEQAAGRESHRQELAAAEAARLQQLEELKAAHQQELEHLRETLDKEKAESLSRLQEELAETRDSLGGEIVEIRSALSKELADTKSTLEKELAEEREALQKELAKNKELRQSQGTQEHRHKQQMQEMEKQIGELRGGTGQLQSRLRAAEAGLKSEREGRLTLLAQYEAVLKREEQLTEELRAAAEQGTLRQEELEALRQRYEAVQQEAAGLKESLRGTAENLSRVETELHSANELGDLLSDELEELRQRHSRKQEEAAVLHQSLEETKSSLHQLEGELAQAASEAAAWHELADKHMEDIGELEMKLLEAEEKSSALQTEIDTLRGQADGMVQQLDRESGLRAEAEAESRQYRAEAEAARKELAALRGRYEELIAQYDEVLQDGEQLKERYELLEAEGEETARRLEELYEAGREAAAAAAEQQEALRETREVEASWKRKYEELLQSQQEWSETEAQLREEIEIWEQEASKAEAEAESMNREHSQVQQQLDEIGESYELVQGQLRLLQAQSEMRQGELDKLSQEHQSLQAEYAKLQREYNEWIQLIEQDS
>NZ_LN831776.1|WP_020432752.1|2502305_2504753_+|phenylalanine--tRNA-ligase-subunit-beta
MKVSTSWLADYISLEGVTAAELADRITTAGIEIDGVERRNKGLSGIVVGYVKSKEKHPDADKLNVCIVDAGQGEDLQIVCGAKNVAAGQKVPVALVGAKLPGLEIKKAKLRGVLSQGMICSAKELGLNDKLLPKELQEGILVLPENTEIGQDILKVLGLNDEILDFDLTPNRSDCLSMIGAAYEVSAILGRDLKLPDPAADLVEAGGLASDSISVKIENEEYCRHYSVRYISGVKPAPSPLWIQNRLMAAGVRPINNIVDITNYVMLEYGQPLHAFDGDKVEGGVLGVRFAREGELLTTLDGQERKLEPQMLVIADGAGKAVALAGVMGGLETEVTEATVNLVLESAKFDGGTVRKTSRQLGLRSEASLRFEKEVDPNAVIPALNRAAALIARYAGGTVHTGIVQAGTAAAEEKVLTLSLEKLNRYLGTDLSLLEVKTLLTRLHFKCGDADQGLVEVQVPTRRGDISYDVDLIEEVARLYGYDNIPTTLIEGVTTPGALTSRQFQRRELRRLLADGGFQEVMGYSFIQPEQSKLFPALADGLLPVKLAMPMSEERSVLRTSLIPQLLDIARYNTNRRQSDLALFEIGNVFFTDEEQLTRQPRELPVLGLLLSGSRASKQWNVEEQPVDFFDLKGALETVFNYLGLGDSVSYEGDAPENYHPGRSASIYLQGPEGRVKLGTLGQLHPELQRELDLEDTYVAELLLQPLYSAARTNLQYTELQRFPGIERDIAVVVDSAVPAGHLLASIRENGGTLLQNVQVFDVYTGGKMESGKKSIAISLLYRHTDHTLTDEEVVEVHDKVVSALQQTFGAELRK
>NZ_LN831776.1|WP_020432757.1|2500930_2501965_+|phenylalanine--tRNA-ligase-subunit-alpha
MKEKLEALKVEALAKLQEVTDPQLLNDLRVKYLGKKGELTEVLRGMGGLSAEERPVIGQVANLVRSAIEEIISTKQEAFQQQETLNRLNAEKVDVTLPGRRLPQGGIHPVSRVVREIEDIFIGMGYRVAEGPEVETDYYNFEALNLPKNHPARDMQDSFYLTEDILMRTQTSPVQIRTMQAMKGETPVKIICPGKVFRRDDDDATHSFQFHQIEGLVIGRHIRMSDLKGTLQQFVQEMFGPNTGIRLRPSFFPFTEPSVEVDVSCFKCGGHGCRLCKQSGWLEILGAGMVHPNVLEKGGYDPAEYSGFAFGMGVERIAMLKYGIDDIRYFYTNDMAFVKQFKGI
>NZ_LN831776.1|WP_052741438.1|2498289_2499894_-|diguanylate-cyclase
MAGFPEIKNTRRLILLFTAISVLLVGISVASLLYLNHTMNKLSDSLYSDVYQNSQLILNADRDLYQASLAFHTAMNGNLTSGEYSRLSRDFQENNAQAERRLRMASDNINSVKNPFSEMRQSELLLSKLRETLGSIDAPFQIWKDTGTNLMARRVRSGWNPESYSALEANVLLKNVREPLDNSERLIDGYARQVTQEFRDQKSSLFALYSLFLFLLVLVIIYLCRKLIDLQNEMLEEKSLYQLIGETMSDFIILTDSNGQILYASPSHSSLLGYLPGRGTPLTNYIREAEITWVKLKSVVQSTPRISELRMRAGDGHWVWLETKVTPIKGGGAVPAQFMLVSREITERKQHEERLHKLAFYDHLTAIPNRAHFKMYMENLISQPEERKQEIALALLDCDRFKQLNDTLGHLAGDEFLQLLSRELQQTVKGTGQAFRIGGDEFAVVLHRFASPEMLDEILDRLLQLFNKSWSVNKGSSFHTSASIGVALYPQHGSSINELLRAADLAMYRSKKHGGNEANLYSELVDEEYKDQPK
>NZ_LN831776.1|WP_020432771.1|2495754_2498151_+|type-I-pullulanase
MNSNYINTEKEIEIYTGKDLGLTYTADYSLFKVWVPTAFTVSLVLYQTDGNNIEGMVSGYRDSGRIVNMQRQEGGIWQARLHEDLKGMYYMYRAVFEDGTLNEAADPYAKAVSANGVRSAIVDLQDTDPEGWDRDVSPALPHPADAVIYELHVRDFSAAADSGMRYKGKFKAFTEFGLKNSAGQAIGVDHLAELGITHVHLMPVADFQTVNELGVNSERSAEPFFTEYNWGYDPQHYNVPEGSYSTNPSDPGTRIREMKEMVQALHSKGISVIMDVVYNHTYSVEKGPFQPLVPDYFYRHDYTGRLSNGSGVGNELATERPMVRKYIKDSLAYWASEYHIDGFRFDLMGLMDSVTMREIAEELRLEVNSDLLLYGEPWTGGDSPLATKTLKGVQKGKGYAVFNDNFRSAVKGDSDGWGKGFATGEYGKEGAVASGIKGAIHEFTDSPVETVNYVTAHDNLNLWDKVLATQGLRQAARLPELENGRLKYGGSVEAAVAAADPYIGMDPDDILGNETVRRTLLANGIILTSQGIPFLQAGDELLRSKYGDHNSYRSPDAVNAIRWENKGKFLPVFEYYKGLIALRSGHPAFRLHGRQEIERSLEFLRCDSGVVAYLLKNNAGGDVWNNIVVIFNANPGPVSQRLPETDSCWNIVVDHTAARTDAFRSVQDPEVQIEGLSMMVLYDKYGQPEPRSKVIEIRYERPDGDYRGWNLWVWGTGIQDGQHDFRQMEDGGAVARIEVLPETSSVGYILRLNDWEEKDSAGDRFIDCSGSREGVKVTIRDREQENSGDKNDPLQMTS
>NZ_LN831776.1|WP_046502156.1|2493645_2495358_+|phosphoenolpyruvate--protein-phosphotransferase
MSKISGIAASAGIAVARAFILEHPDYTITKTAAADVEAEIAKLTDALEKSKAELQSIKERTLAELGEKKAEIFESHLLILDDPELISPVMDKIREEMVNADYALNEVATQFIEMFENMKSAYLQERAADMRDVTKRVLNHLLGIHYVSPAEISEEVIVIAQDLTPSDTAQLNRNFVKGFTTNIGGRTSHSAIMARSLEIPAVVGTKNVLSEVKAGDLVIVDGLSGDVLINPSDAEVAEYKAKQAAYDLQIAEWKKLRDEPTVSADGKHVELAANIGTPNDVNGVIDNGGEGVGLYRTEFLYMGRDKLPSEEIQYNAYRTVLENMKGKPVVVRTLDIGGDKELPYLDLPKEMNPFLGFRAIRLCLDRQDIFRTQLRALLRASAHGDLRIMFPMIATLGEFRAARDLLLEEKAKLREEGKEVSDSIQLGIMVEIPSTAVLADQFAKEVDFFSIGTNDLIQYTMAADRMNERVSYLYQPYNPAILRLVKTVIDAAHAEGKWAGMCGEMAGDSTAIPLLLGLGLDEFSMSATSILPARSQISKLSAAEMKEMAAKALQLSTAEEVAALVQSSVK
>NZ_LN831776.1|WP_039790804.1|2493377_2493653_+|HPr-family-phosphocarrier-protein
MQKTFRIIDEDGIHARPATALVNTATKFKGTESFAEAKGKKVTLKSILGVLSLGLEAGDTLTLITEGSEEAEALSALQEVMVKEGLGELHE
>NZ_LN831776.1|WP_020432774.1|2491214_2493278_+|PTS-transporter-subunit-EIIC
MFKKLFGVLQRVGKALMLPVAILPAAGLLLGIGNMLVNPDFLQYVPALENDVVQAVATVLMNSGQIVFDNLSLLFAVGVAIGLAGGEGVAGLAAIIGFLVMNVTMGTVVGVNAYVLSWKDYAYSSVLGIPTLQTGVFGGILVGILASAMYKRFFRIELPSYLGFFAGKRFVPIMTAVTSLLLGLLLTLIWPPIQHGLNYVSQSMINTNLTLSAFIFGVIERSLIPFGLHHIFYSPFWYEFGSYVDKAGDLIRGDQRIFMQQLRDGVEFTAGTFTTGKYPFMMFGLPAAALAIYHEARPENKRVVGSLMISAALTSFLTGITEPLEFSFLFVAPLLFAVHAVFAGLSFMTMHILNVKIGMTFSGGFIDYMLFGVIPNRTAWWLVIPVGLVLAVIYYFGFRFVIRKFNLRTPGREDPSDDVEETDTENVSRSGDDLPRNILSALGGKENITHLDACITRLRVEVKDKAGVDKNRLKKLGASGVLEVGNNVQAIFGTRSDTIKSQIQDVMDGRTPAASPAAAAPQPELEKQAGEEGAAIIPEDIVSPVNGELLDITQVPDAVFSQKMTGDGFAFLSDDGKIASPVYGKVFNVFPSKHAVGIMSDGGKEVLVHIGVNTVKLKGKGFTVLVEEGDLVAAGQPIMEVDLEYVKANAPSVISPVIFSNLPEGSAVTLKKPGKVVIGDKDIISIM
>NZ_LN831776.1|WP_046502153.1|2490021_2490891_+|PRD-domain-containing-protein
MSSITVAKVLNNNVIIAQHPQYAEVVVIGKGIGFNRKVRDMINLSSVEKMFILRNQEEQEQYKQLVPQVDEKLIEVVQEIVLHILQNSRQPLNEHIHIALTDHISFAIRRNEQNIAIHNPFLYETKEIYPEEYSLAEYAVGRINEAMGVKLPSDEIGFVALHIVSALSNRHISEVKEHSLLIGDLVNLVEDHLEYHIPRDSLDYSRLVTHLRFVLERLRRGETVRETSSLDGLMKREYPEMYMLAWKLTKVIEKRVRIPVYAAEVSYLTIHLQRLAQKKEDEADMQQPD
>NZ_LN831776.1|WP_167345604.1|2488260_2489886_+|hypothetical-protein
MAAMISTLNTIMKIRGASGANRLLYYFGRLPLIGKLMNDNVYSKASLKKTFTIAVLILKMIWGFLSKFAYLGLVVYLPVQLAVKELPIAEQYDLYLYILVLLSFGVGAVSNAIILEPKRDKYICVKLMRLPADKYMHAVMALRALTFFVYFIPAMVVFARAYGAPLWQGLLLSLLLSLWRIAGEALHLWIFDRKEIVLVKKNGLVWTVIGAGYLLAYVPLYMGSSLLDMDNMLFSLPLSLALVVLGAVSAWYIARYAGYRNAVDAVTKIDDPLLDMGRMMKEASMKQVETKEKDFSAEKLRPGQFAGKSGFAYLNAIFFSRHKRFLIQPIQRRLVIIGALSAAGLLAMFAAPDAFSKLARYLISSLPVLVIAMNFTSIGERVCKAMFFNCDLSLLRYGFYRERSAILSNFRTRLLRISGLNLIPAAAICVGVNLLLFLSGEHWGVGEALIVSCAILGLSLFFSVHHLFMYYIFQPYSTELNVKNPFFSIVNSIVLAVGVVCMQFQSSPARFAMVVLLAAAAYMLIALFLVYKYSSRTFRVK
>NZ_LN831776.1|WP_020432744.1|2507732_2508125_-|hypothetical-protein
MIRRFAMLLSIGSLLILAACGGTGNNTGTASNKDGAAETGLTADEELIISATNYSFDQKEYHLKKGVPVNIVFKNESGNHGILVPELNLRLDGKDSSQVIVPEEAGTFEMTCAIMCGSGHSSMSAKVIVE
>NZ_LN831776.1|WP_052741439.1|2508385_2509471_+|GGDEF-domain-containing-protein
MTGYWIIVFCMLVAQLLYVLSNHVIEVRSILLPSKGHLFIGCNLMIVIAMATAEMWLRSTSLYHKQAVVVCGFAVSYLMYFVLEPFVDGAQMTLMMPIMISLVYFDQRLLNALGAFSLLFYAAIYLGLEQRLLDKPLLEFLMVECVFIVFVVMAQAVIIRAREVREHLEQLTKSEQELMVERAISDKLLKIDALTGLYNHKTFHEYLVSLLEQCESNGLRLQLALFDIDNFKRVNDTYGHWVGDLVLKEVAAKVGGLIGLNDFAARYGGEEFAVIFTDKSIHEAYAAAEELRLKIAAMEHPYAGGKPITVSIGLCDYQLGDGKEKLFRKTDHALYAAKHSGKNAVVTASAAHDDDNILSYA
>NZ_LN831776.1|WP_020432741.1|2509551_2509899_-|phage-holin-family-protein
MRFLGHVVRFIVAAIVLMVVGWIVPQFTVGGFWSALVLALVIALLGWVIEGIFGKKTTPFGRGIVGFLVSALVIWIAQFIVSGVSVTVLGALLAALVIGIIDLFLPVSTPFEAGK
>NZ_LN831776.1|WP_046502162.1|2510052_2512419_+|endonuclease-MutS2
MDDKILHTLEYRKILNKLTQYTQTPMGRLEAESLKPSGDFEGVKKLLQATDEAANVDRLKGIPSFGGVTDIKMALKRASIGGLLGTSELLSVGNTIGGARRVKRFLAAMHEDENIPLLFAQSDLLSEQKHVEDAIRACIDENADVLDTASPELAAIRRELRGGETRIREKLDSMIRSSSVAKMLQDQLVTIRGDRFVIPVKAEYRAHFGGIVHDQSGSGATLFIEPESIVAMNNKLRETRLREEREIEIILHRLTALVGDIAEEMAYDVDILGELDFIFAKARLARDMKATQPRMNDRGYLKLRKGRHPLIPAEQVVPLDVELGNQYSSIIVTGPNTGGKTVTLKTIGLLSLMSMSGLFIPAEEGSQMCVFDAIYADIGDEQSIEQSLSTFSSHMTNIISILRRMTPKSLILLDEVGAGTDPAEGSALAIAILENIHRTECRMVATTHYSELKAYAYERKGVINASMEFDVQTLSPTYRLLVGVPGRSNAFAIAERLGLPNEILEHARGEVKEEDLRVEHMIASLEENRLGAENERERAEAVRREAEEFRKRQQLELEKLESQRDKRLEKAEKDASAILDKARKEAEQIISDLRRLALEEGASVKEHKLIEARRRLDEAEPAPRKKTAARSSVKAPRKIQPGDEVKVQNVNQKGYVVELSGPKEAIVQFGIMKMKVNLEDLEFLASAPDSPPPALRRATTVKRTRDENIRSELDLRGTNLEEAIMETDRFIDEAFLGNLGQISIIHGKGTGVLRTGIQEYLRKHKHVKSYRLGNYNEGGAGVTVAELQ
>NZ_LN831776.1|WP_020432739.1|2512450_2512870_+|DUF350-domain-containing-protein
MQENIDLLLDHPLGALLGYFTVAILGLVVFLSFFEMVTKYNCWEEIRKGNVAVAMATGGKIFGICNILRFSISAGVSIYETMKWSVVGFLLLILAYFLFEFLTPVFSIDDEIAKDNRAVGLTAMMISVSLSYVIGAAIF
>NZ_LN831776.1|WP_046502166.1|2513000_2513546_+|hypothetical-protein
METTVCPWCHTEIVWDEEFGPEDTCPHCNNELSGYRTVTLGIDDLEDEDEPEMAGEPDQDPVSDENLWNDEDKESVVPIFNTLVQFGEDYDLKHYESKVAAILAAQLEAPECPQCHELMLLSGTQKVEGFEPSSPDELGGPVLQPPFALNLFVCPSCFHVQHSLAQEDRIQLVRNLSIGAK
>NZ_LN831776.1|WP_046502169.1|2513616_2514831_+|MFS-transporter
MKDSAHKQEVLLLAVNGLCSLASVLAGTFLNVYLWKNQQNFAMIGWFTVAQQVTVGLSFWLGGKWVKEHNKMNALRLGLAVSGLFYLLVLWLGNRAVHYIWPLGLVLGIAIGLFWLAYNIVYFEITDAGNRDFFNGWMGLLGSFTGILGPWVSGWIISALHGERGYRLVFLLSLSIYGLAVVLSFFLKKRKSEGAYLWMEPWRELHRKSSAWRPAAAALVFQGLREGVFSFLIGLLVYIAAKQESKLGQFALITSAVALVSYWAAGKWFTPKLRSGGMLVGGILLVAVITPLLWKVSYGTLLIMGIGTSLFLPLYMLPMTSSVFDLMGESKESAGKRVELVVLRELCLMCGRMLGIFVFIAVLSVNDSPRVITWLLLLLGAAPLGSWAALHHLLKRKAAASLPQ
>NZ_LN831776.1|WP_020432735.1|2514863_2516474_+|two-component-system-sensor-histidine-kinase-DcuS
MVKTKDYGLRTKVTIMVSAVVMLVMLVLYIIFRNQIIPQTRHALEDKATAIARTIALIPLVSEGLNEGRSKEIQAYTSKITRRNDIMFVVVIDMHSIRYSHPDPSRIGKPFVGGGQKAALHGEESISEGEGLLGKSLRAFVPVYNNRGSQVGVVVVGLSMERVHLLIRQNEWTIIAILLSGAVLGAAGAMVLARKIKQMMFGMEPADISKLLQERSAMLQSTREGIIAVDHAARISMINREAERLLGTAGITGNGMTRHIADYWPELRLEQVLSSGESRQDQELELNGITLLVSSVPIQVNGRIAGAIATFRDKTELAVLAERLSGISVYADALRAGAHEYMNKLHVIMGMTHMGLFDELQEYISGTVSNYQNEIGSITRQIKDPVMAGFLLGKLSRAREAGIELQLAEDSYLPESADPQVIHQLITIVGNLLDNAMEVLEGQHMKEIELSFQYERGRLICTVRDNGPGIPEPLREQIFVQGFSTKGEQRGMGLYLVRKSVEKLQGQLKMIPGREPGTIFMADVPYAVKGDETNDH
>NZ_LN831776.1|WP_020432734.1|2516463_2517180_+|response-regulator
MTIKVLIVEDDPMVAKFNRHYVEQVQGFEFAGWAASVDEARKLLAGLKVDLILLDIYMPRTSGLQLLSSLREQGSVVDIIVISAASDNASIRKALQLGAVDYLIKPFEFARFQAALSAYQEDYMLMKHREHLSQEQLDKLLRHSTGTEEDKSGALPKGLTEGTLESIWSTIQKLESPVFSTEEITAEAPISRISVRKYLTFLTEAGVLEMEISYGAVGRPVYMYTVTASGHEIIAAYI
>NZ_LN831776.1|WP_020432733.1|2517890_2519423_+|flavocytochrome-c
MKKKTGAALILILSVMLVIAGCGSNGNSNSAGNKSKDNEAKKETTEAVSGASEASYTPYDQLKDKYDIIIVGAGGAGMSAALEAKAKGMNPVILEKMPVAGGNTTKSSSGMNASQTKFQKEQGIEDSNDLFYEETLKGGHDTNDKELLRFFVDNSAGAIDWLDSIGIRLNNITITGGMKEKRTHRPEDGSAVGQYLVKGLVKNVQEQGIPLFVNADVKEITEKDGKVTGVKVLFNQADEKTITGSAVIVTTGGFGANKEMIAEVRPDLEGLVTTNQVGSTGDGIKMIEKLGGTTVDMDQIQVHPTVQQEKSYLIGEAVRGEGAILVSSEGKRFTNEMDTRDHVTAAINKLPEKAAILVFDSGVKSRVKAIEQYEKMGFVLTSDSIEGLAKEMNVPADELQKTMDTWNSAVKNKKDAEFGRTTGMDNDLSGAPFYAIKIGPGIHYTMGGVKINTNTEVLNKEGQPITGLFAAGEVVGGLHGQNRIGGNSVAEIIIFGRQAGIKSAEFVKAQ

Crispr_ID: NZ_LN831776_32

• CRISPR_ID: NZ_LN831776_32
• CRISPR_location: 2606655-2606729
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_32

Consensus_repeat	Method
AATAACGGCAGAAATGCCGTTGTT	CRISPRCasFinder

spacers of NZ_LN831776_32

>32.1|2606679|27|NZ_LN831776|CRISPRCasFinder
GAAGCGCCGAAGGCTGGTTTGACCATA

CRISPR arrays and Neighbor proteins around NZ_LN831776_32

CRISPR arrays

The CRISPR arrays of NZ_LN831776_32

>merge|NZ_LN831776|32|2606655-2606729|CRISPRCasFinder
AATAACGGCAGAAATGCCGTTGTTGAAGCGCCGAAGGCTGGTTTGACCATAAATAACGGCAGAAATACCGTTGTT

>NZ_LN831776|32|34|2606655-2606729|CRISPRCasFinder
AATAACGGCAGAAATGCCGTTGTT	GAAGCGCCGAAGGCTGGTTTGACCATA
AATAACGGCAGAAATACCGTTGTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020428040.1|2603321_2603729_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020433720.1|2614790_2617175_-|transglutaminase-domain-containing-protein	unknown	unknown	gnl|CDD|376628
NZ_LN831776.1|WP_020433725.1|2610208_2612104_+|PrkA-family-serine-protein-kinase	unknown	unknown	gnl|CDD|225357
NZ_LN831776.1|WP_020428039.1|2602257_2603325_-|phosphodiester-glycosidase-family-protein	unknown	unknown	gnl|CDD|378342
NZ_LN831776.1|WP_020433717.1|2617671_2619066_-|SpoVR-family-protein	unknown	unknown	gnl|CDD|377285
NZ_LN831776.1|WP_046502227.1|2609184_2610033_-|hypothetical-protein	unknown	unknown	gnl|CDD|227769
NZ_LN831776.1|WP_020433715.1|2619535_2620549_-|bifunctional-glycosyltransferase-family-2/GtrA-family-protein	unknown	unknown	gnl|CDD|133022
NZ_LN831776.1|WP_039790642.1|2607618_2608314_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224054
NZ_LN831776.1|WP_020428036.1|2600909_2601374_+|tRNA-(uridine(34)/cytosine(34)/5--carboxymethylaminomethyluridine(34)-2'-O)--methyltransferase-TrmL	unknown	unknown	gnl|CDD|349967
NZ_LN831776.1|WP_020428035.1|2599688_2600777_+|3-phosphoserine/phosphohydroxythreonine-transaminase	unknown	unknown	gnl|CDD|235428
NZ_LN831776.1|WP_039787771.1|2598694_2599579_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020428042.1|2604734_2605952_+|PLP-dependent-aminotransferase-family-protein	unknown	unknown	gnl|CDD|224089
NZ_LN831776.1|WP_020428041.1|2604009_2604666_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225107
NZ_LN831776.1|WP_020428037.1|2601497_2601752_+|AbrB/MazE/SpoVT-family-DNA-binding-domain-containing-protein	unknown	unknown	gnl|CDD|131898
NZ_LN831776.1|WP_046502224.1|2608339_2609113_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020433723.1|2613103_2613592_-|DinB-family-protein	unknown	unknown	gnl|CDD|378981
NZ_LN831776.1|WP_020432627.1|2592894_2594319_+|type-I-glutamate--ammonia-ligase	unknown	unknown	gnl|CDD|273198
NZ_LN831776.1|WP_046506726.1|2595573_2598309_+|cellobiose-phosphorylase	unknown	unknown	gnl|CDD|213065
NZ_LN831776.1|WP_046502232.1|2613783_2614677_+|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|226231
NZ_LN831776.1|WP_167345605.1|2612248_2612806_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020433720.1|2614790_2617175_-|transglutaminase-domain-containing-protein	gnl|CDD|376628	pfam01841, Transglut_core, Transglutaminase-like superfamily. This family includes animal transglutaminases and other bacterial proteins of unknown function. Sequence conservation in this superfamily primarily involves three motifs that centre around conserved cysteine, histidine, and aspartate residues that form the catalytic triad in the structurally characterized transglutaminase, the human blood clotting factor XIIIa'. On the basis of the experimentally demonstrated activity of the Methanobacterium phage pseudomurein endoisopeptidase, it is proposed that many, if not all, microbial homologs of the transglutaminases are proteases and that the eukaryotic transglutaminases have evolved from an ancestral protease.	1.48913e-09
NZ_LN831776.1|WP_020433725.1|2610208_2612104_+|PrkA-family-serine-protein-kinase	gnl|CDD|225357	COG2766, PrkA, Putative Ser protein kinase [Signal transduction mechanisms].	0
NZ_LN831776.1|WP_020428039.1|2602257_2603325_-|phosphodiester-glycosidase-family-protein	gnl|CDD|378342	pfam09992, NAGPA, Phosphodiester glycosidase. This is a family conserved from bacteria to humans. The structure of a member from Bacteroides has been crystallized and modelled onto the luminal region of the human member of the family, the transmembrane glycoprotein N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase. There is some conservation of potentially functional residues, implying that in the bacterial members this family acts in some way as a phosphodiester glycosidase. The human protein is also present, so the eukaryotic members are likely to be catalyzing the second step in the formation of the mannose 6-phosphate targeting signal on lysosomal enzyme oligosaccharides.	5.36241e-32
NZ_LN831776.1|WP_020433717.1|2617671_2619066_-|SpoVR-family-protein	gnl|CDD|377285	pfam04293, SpoVR, SpoVR like protein. Bacillus subtilis stage V sporulation protein R is involved in spore cortex formation. Little is known about cortex biosynthesis, except that it depends on several sigma E controlled genes, including spoVR.	0
NZ_LN831776.1|WP_046502227.1|2609184_2610033_-|hypothetical-protein	gnl|CDD|227769	COG5482, COG5482, Uncharacterized conserved protein [Function unknown].	3.63892e-51
NZ_LN831776.1|WP_020433715.1|2619535_2620549_-|bifunctional-glycosyltransferase-family-2/GtrA-family-protein	gnl|CDD|133022	cd04179, DPM_DPG-synthase_like, DPM_DPG-synthase_like is a member of the Glycosyltransferase 2 superfamily. DPM1 is the catalytic subunit of eukaryotic dolichol-phosphate mannose (DPM) synthase. DPM synthase is required for synthesis of the glycosylphosphatidylinositol (GPI) anchor, N-glycan precursor, protein O-mannose, and C-mannose. In higher eukaryotes,the enzyme has three subunits, DPM1, DPM2 and DPM3. DPM is synthesized from dolichol phosphate and GDP-Man on the cytosolic surface of the ER membrane by DPM synthase and then is flipped onto the luminal side and used as a donor substrate. In lower eukaryotes, such as Saccharomyces cerevisiae and Trypanosoma brucei, DPM synthase consists of a single component (Dpm1p and TbDpm1, respectively) that possesses one predicted transmembrane region near the C terminus for anchoring to the ER membrane. In contrast, the Dpm1 homologues of higher eukaryotes, namely fission yeast, fungi, and animals, have no transmembrane region, suggesting the existence of adapter molecules for membrane anchoring. This family also includes bacteria and archaea DPM1_like enzymes. However, the enzyme structure and mechanism of function are not well understood. The UDP-glucose:dolichyl-phosphate glucosyltransferase (DPG_synthase) is a transmembrane-bound enzyme of the endoplasmic reticulum involved in protein N-linked glycosylation. This enzyme catalyzes the transfer of glucose from UDP-glucose to dolichyl phosphate. This protein family belongs to Glycosyltransferase 2 superfamily.	6.23937e-33
NZ_LN831776.1|WP_039790642.1|2607618_2608314_+|ABC-transporter-ATP-binding-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	2.69559e-66
NZ_LN831776.1|WP_020428036.1|2600909_2601374_+|tRNA-(uridine(34)/cytosine(34)/5--carboxymethylaminomethyluridine(34)-2'-O)--methyltransferase-TrmL	gnl|CDD|349967	cd18094, SpoU-like_TrmL, SAM-dependent tRNA methylase related to TrmL. tRNA (Um34/Cm34) methyltransferase TrmL catalyzes the methyl transfer from S-adenosyl-L-methionine (AdoMet) to the 2'-OH at position 34 in both tRNA(Leu)(CmAA) and tRNA(Leu)(cmnm5UmAA). It is part of the SpoU family of MTases, a subfamily of the SPOUT methyltransferase superfamily. The SPOUT methyltransferase superfamily is a large class of S-adenosyl-L-methionine (AdoMet or SAM)-dependent RNA MTases which are structurally characterized by a deep trefoil knot.	6.64314e-88
NZ_LN831776.1|WP_020428035.1|2599688_2600777_+|3-phosphoserine/phosphohydroxythreonine-transaminase	gnl|CDD|235428	PRK05355, PRK05355, 3-phosphoserine/phosphohydroxythreonine transaminase.	0
NZ_LN831776.1|WP_020428042.1|2604734_2605952_+|PLP-dependent-aminotransferase-family-protein	gnl|CDD|224089	COG1167, ARO8, Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs [Transcription / Amino acid transport and metabolism].	4.11538e-103
NZ_LN831776.1|WP_020428041.1|2604009_2604666_+|response-regulator-transcription-factor	gnl|CDD|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	5.49316e-30
NZ_LN831776.1|WP_020428037.1|2601497_2601752_+|AbrB/MazE/SpoVT-family-DNA-binding-domain-containing-protein	gnl|CDD|131898	TIGR02851, stage_V_sporulation_protein_T, stage V sporulation protein T. Members of this protein family are the stage V sporulation protein T (SpoVT), a protein of the sporulation/germination program in Bacillus subtilis and related species. The amino-terminal 50 amino acids are nearly perfectly conserved across all endospore-forming bacteria. SpoVT is a DNA-binding transcriptional regulator related to AbrB (See pfam04014). [Regulatory functions, DNA interactions, Cellular processes, Sporulation and germination].	7.9209e-12
NZ_LN831776.1|WP_020432627.1|2592894_2594319_+|type-I-glutamate--ammonia-ligase	gnl|CDD|273198	TIGR00653, Glutamine_synthetase, glutamine synthetase, type I. Alternate name: glutamate--ammonia ligase. This model represents the dodecameric form, which can be subdivided into 1-alpha and 1-beta forms. The phylogeny of the 1-alpha and 1-beta forms appears polyphyletic. E. coli, Synechocystis PCC6803, Aquifex aeolicus, and the crenarcheon Sulfolobus acidocaldarius have form 1-beta, while Bacillus subtilis, Thermotoga maritima, and various euryarchaea has form 1-alpha. The 1-beta dodecamer from the crenarcheon Sulfolobus acidocaldarius differs from that in E. coli in that it is not regulated by adenylylation. [Amino acid biosynthesis, Glutamate family].	0
NZ_LN831776.1|WP_046506726.1|2595573_2598309_+|cellobiose-phosphorylase	gnl|CDD|213065	cd11749, GH94N_LBP_like, N-terminal-like domain of Paenibacillus sp. YM-1 Laminaribiose Phosphorylase and similar proteins. The glycoside hydrolase family 94 (previously known as glycosyltransferase family 36) includes bacterial laminaribiose phosphorylase. This N-terminal domain is involved in oligomerization and may play a role in catalysis, but it is separate from the catalytic domain [an (alpha/alpha)(6) barrel]. Bacterial laminaribiose phosphorylase phosphorolyzes laminaribiose into alpha-glucose 1-phosphate and glucose, but does not phosphorolyze other glucobioses; it slightly phosphorolyzed laminaritriose and higher laminarioligosaccharides. The GH64N domain, as represented by this model, is also found at the N-terminus of GH94 members with uncharacterized specificities.	1.42707e-124
NZ_LN831776.1|WP_046502232.1|2613783_2614677_+|AraC-family-transcriptional-regulator	gnl|CDD|226231	COG3708, COG3708, Uncharacterized protein conserved in bacteria [Function unknown].	1.14341e-32
NZ_LN831776.1|WP_020433723.1|2613103_2613592_-|DinB-family-protein	gnl|CDD|378981	pfam12867, DinB_2, DinB superfamily. The DinB family are an uncharacterized family of potential enzymes. The structure of these proteins is composed of a four helix bundle.	3.74466e-07

Protein sequences

>NZ_LN831776.1|WP_020428042.1|2604734_2605952_+|PLP-dependent-aminotransferase-family-protein
MKYEFSARAHTLHSSTLLSIRTETRRGTLISLAEELPAEELFPLSLLAETASTVISADAGALQYGDPEGYGPLREWLTGDWLKAKGVAVAAGGVLLTTGSQQAIDLLSRVYIDPGDRVLVENPTSPGILQALRMQGAVIIPVKGDQDGLLPEHLRTQIRLHRPKMLFATPSFTNPSGILWSLARRKEVLELCTTHNLLIVEDDSYGDLHFQRYTEHPSVKYPSLYALENVSEGGHVLYIGSFSKTVAPALRTGWAAGSRELIGMMAAAKQMADWQSSSLNQRLLHHLLDVTAFDLREHIALLNREYNTRLKLMAELLKRPAWKSSSYCLPAGGMFLWVTLPEGLDAMALLKASLAKGVAFLPGPLCSVSGGSGRIRLNFSHPGRDELLLGMNLMSEAVTEFTARS
>NZ_LN831776.1|WP_020428041.1|2604009_2604666_+|response-regulator-transcription-factor
MMKVWRVIIVGCHPTSMLGTKLILEESKEIEVVGMFSNWSEGVHTVQQQQPDLVLTDYQMPEGNVEGALVEMKQSSKSTHFIIMTEEEDKELFQPLIELGASGVLSKGASPRQLLQMISGLREGFLSIPLEWAQDGFRPVASSRGLDGVLQLTQTEMFIMERIVQGITYDKIALEIEVSRRSIDNYLRKIYVKLEVSTRAQAIEKFALFSRQNKQMYA
>NZ_LN831776.1|WP_020428040.1|2603321_2603729_-|hypothetical-protein
MQPLAESTPVHSRRTSARNGSSVKWFLLFWIVMIGLGFYAVYSYTNHLKEQVLSSLSTQSQQQLTVLKTDYESRIGVLSQQVKELQSTVDTFNELLTFTKDNASNKTDNSNKLYTQLNEVRKQLAALQKEMDLLK
>NZ_LN831776.1|WP_020428039.1|2602257_2603325_-|phosphodiester-glycosidase-family-protein
MMTPVKRVNRFFMLLTAPFLGLLLCLWWYQPPLDLNLDVGQFAAEPGPIKETAELQSALTTAQAAASYTIHSISASAKLYNQTTNAMNALVQMAKTQAARPELIYNRRISSRLGIPADVARSDRITIELYRLNPGNYTAYAMKIKLKDPSAMKMSLAGDGKGGAETTLQAANRYGATAGINAGGFADRAGKRYPLSTTVIGGEYLYGFESTYKDLSFVGLNASGQLIGGKFYSRTQLDQLQPVFGATFVPVLLKNSVKVPIPAKWQLSPKRAPRTVIGKYKDDQLLVMVADGYNENGNSGATLEELQNKLSNMGVIDAYNLDGGGSSSLIFNGRVINKPSDGNLRKVPTNFLFFK
>NZ_LN831776.1|WP_020428037.1|2601497_2601752_+|AbrB/MazE/SpoVT-family-DNA-binding-domain-containing-protein
MKPAGVVRKVDQLGRIVLPKSLRKRYQMNEGDPVEILVQGDHIILERYRPKCVFCGSMEGVSEYKDRYICADCLTEMTQLSRHA
>NZ_LN831776.1|WP_020428036.1|2600909_2601374_+|tRNA-(uridine(34)/cytosine(34)/5--carboxymethylaminomethyluridine(34)-2'-O)--methyltransferase-TrmL
MALHIVLVEPEIPANTGNIARTCAATGTHLHLVRPLGFRTDDATLKRAGLDYWHAVHIEYHDSFGEVLEKYAEGRFFYATTKADKRYTDFTFRDGDFFVFGKETKGLSAEILEAGKETVMRMPMSEAVRSLNLSNSAAIIVYEALRQLNFPQLF
>NZ_LN831776.1|WP_020428035.1|2599688_2600777_+|3-phosphoserine/phosphohydroxythreonine-transaminase
MSKRAYNFNAGPAALPLTVLERAQAEFVDFRESGMSIMEMSHRGAIYESVHNEAQERLLSLLGNPQGYKVLFIQGGASTQFAMIPMNFVTEGKVGSYVMTGSWAEKAFKEAKLVGGAHAAASSEDKKFLAIPELSSIKAADNAAYLHVTSNETIEGTQFAEYPDAGSIPLIADMSSDILSRSFDVNQFELIYAGAQKNLGPSGVTVVIVKEELIAKSPSNIPTILRYDTHLKNNSLYNTPPSFSVYMVNEVLKWIEEQGGLAGIEVKNRDKAALLYDHIDGSGGFYRGVAEAGSRSIMNVTFRMQSEELEKQFVKAAEQEGFVGLKGHRSVGGLRASIYNAVPYESIKALSDFMKHFQQTQG
>NZ_LN831776.1|WP_039787771.1|2598694_2599579_+|hypothetical-protein
MAYSLSNGILQIDIADVGEYSGTRFDWTGFITGVTLLEGGHTYCVPESLVPGHGSGGMGLCNEFGISRAIGYEEAAAGEWFPKLGVGLLQKVSDEPYDFFGNYPLIPFKIEEERSAQSVTYTVQPMECRGYSIRLTKKITLLEDRLNISYLLENMGDKPLHTEEYIHNFVGINGASVGPDYELGIPAGLRVEDPESFYTADLLAVSGNSLTWKAEPERPFYCKLGIWNKMDDGCFWELRHKPSGAGVRESGDFAAERMALWGEKHVISPEVFVNISILPRHSKHWSRSYQFFTL
>NZ_LN831776.1|WP_046506726.1|2595573_2598309_+|cellobiose-phosphorylase
MNQSKTGWVFTGSNGDFRLKQPDRSSFLYFPLVNEGGMMSSVSPKLHGQVTSGHNTFLTPPLSVEDLHNSRASRNFWVYVDGKGAWSAAGNSARQNAGMYGEEAEDSELEAGLLWHRVTRESREFGIKAEITSFVPAGNDKVELMKVVLTNISAEELTVTPTAAVPLYARSADDLRDHRHVTSLLNRIYTSAHGVEVQPALSFDERGHRVNHTSYGVFGAAEGGGKPTGFFPVQEKFIGEGGSLDWPEAVVLNREPQTGAGGGVHREGYEALGGLRFAAAALQPGHSISYVLVLAIGDERIDVAALMDKYGSVRAFDAMLRENKSFWADKVNTVEFHTSDPVADQWMKWVTLQPVLRRLYGNSFLPYHDYGRGGRGWRDLWQDCLALLIMEPGDVRSLLLNNYAGVRIDGSNATIIGQQPGEFIADRNNIPRVWMDHGAWPFLTTMLYLDRSGDLDFLLEQQSYFRDSFMARCRERDASWDASAGSTLQTADGASYTGTILEHILLQNLVPFFNVGEHNNILLEGADWNDGLDMASQRGESVTFTSFYASNLLDLSRLLRILKERKGLETLELAEEMTLLLDSLHDAVDYESVAAKRGLLDRYYAAAPNKVSGVRSELTLDRIADDLARKAEWLVDHLRRNEWIQGNQGDGWFNGYYNNDGERVEGEAGGNIRMTLTGQVFPLLGHAAAPEQIPQIIAAVERNLYDGKIGYRLNTDFGGIQQNLGRAFGFAFGHKENGAMFSHMTVMYGNALYKRGYVKEGRKVLDSLYSLSVNFELSRMYPGIPEYINEQGRGMYTYLTGSASWLLLTMVTEVFGVKGKLGDLLLQPKLMKDQFDQDGKASIRTIFAERGLDVVYTAASGAEYGDYQIHSVTLNGAEVTLQRVSEGVLIPRSVLAALPEEGFHLLQVVLA
>NZ_LN831776.1|WP_020432627.1|2592894_2594319_+|type-I-glutamate--ammonia-ligase
MSVEKVLQTIKENNIEWVDFRFVDLGGRAHHISLPASAVDEETFVNGVAFDGSSITGFRGIEESDMVMMPDPGTIYIDPFTAHPTLNIMCDIFTPDGERYERDPRGIAVKAEEFLQASGVGTAAFFAPESEFFIFDDVRYESGMNSSSYFVDSEEAVWNTNRKDEGGNLAFKVGVKGGYVPVAPVDSQQDIRSEMCRLLSEAGLEIERHHHEVATAGQAEINFRFDTLKKTADNLLTYKYIVQNTARQYGKVATFMPKPLFGDNGSGMHVHQSIFNGDSPLFYEKGAYANLSEMALNYIGGILYHAPALIALTNPSTNSFKRLVPGYEAPVNLVFSKGNRSAAVRIPVAAVTPKGCRIEFRTPDSTANPYLAFSAMLMAGLDGIKKKINPVELGYGPLDKNIYELADEDKEKIRSVPGTLEEALDSLEADYEFLTEGGVFTKDFIDNYIALKRSEAQAVAIRVHPHEYSLYFDV
>NZ_LN831776.1|WP_039790642.1|2607618_2608314_+|ABC-transporter-ATP-binding-protein
MENVLECSNLTKRYGKKVALDNLNLTLPKGRIVGLLGPNGAGKTTLMKLIVSLLRDYRGSITVCGRRPGLDTKKIVSYLPDREFLYPWMTIEECIAFFRNSFADFQLDMAYAMIEELGLDPNEKVKNLSKGMQERVSISLVFARKAKLYVLDEPLAAVDPSTRDKIMRIILEHFDPESSILLSTHLIHDVESLFTDIAVVNEGRVQLYGGIGELQRDYGMPIEEIFKQLVG
>NZ_LN831776.1|WP_046502224.1|2608339_2609113_+|hypothetical-protein
MVQLNQFKLECRKHCAVFAAFTGISVLTNLYFLFSQDQDLSFVFLLVNMVIGILLPVYIYLDYYREFFTGTMPINHLLPLRTSALFGVKSAVFMLGLILVWLPSLLDVFVNPVGLYHQRIMHSDNPALSIAYLVLSKLCSIPAGLAVMGLALAAAKRLRKPLLSHLCIALVMVLVVGIQFALVVRNSWHWSIGTSAAETFKQYANLLTVSPVSRVQPADINESIQWSSVGMNLLVALVAGAIGRYLFNSRKYEILGK
>NZ_LN831776.1|WP_046502227.1|2609184_2610033_-|hypothetical-protein
MAVKHETELYAPLKSFFEKQGYDIKGEVRTCDLVGLRGNEEQPLIVEMKKSFNLALLLQGVERLRLSPNVYLAVERVRDKKGAVNQRWGELTGLCRRLGLGLVTVVFYKTKAPLVEVLAEPGDAPPQVRSGARRRERLLYEFRERSGDYNTGGSTRVKLVTAYREKALRVALALQAAEAEAAEAAGRRAARSGAPGADAAAAGAAASAGGPAAAPGRAEAARGVTPAELRKRSGVPGAAAFLQKNYYGWFFRVGRGRYTLTAAGTAALIEYAAIAEISAGKL
>NZ_LN831776.1|WP_020433725.1|2610208_2612104_+|PrkA-family-serine-protein-kinase
MDIFERIASYRAENDRLAWSGTFKEYIELLKKDPSPAKTAHSRVYDMIKSHGVEDINGRKRYKFFEQEIFGLDRAVEKLVEEYFHSAARRLDVRKRILLLMGPVSGGKSTLVTLLKRGLEQYSRTDEGAVYAIEGCPMHEDPLHLIPLELRPEIERELGVRIEGNLCPSCQMRLKNEYHGDIEQVKVVRVLLSEEERVGIGTFSPSDPKSQDIADLTGSIDFSTITEFGSESDPRAYRFDGELNKANRGLMEFQEMLKCDEKFLWNLLSLTQEGNFKAGRFALISADEMIIAHTNETEYKSFISNKKNEALQSRMIVMPVPYNLRVSEEEKIYAKLIAQSDMKHVHIAPHALRAAAIFSILTRLKESKKQGMDLIKKLRMYDGEEVEGYKEADLKEMQTEYLDEGMSGIDPRYVINRISSALIKNDLKCMNALDVLRAIKDGLDQHPSITKEERERYLNFISIARKEYDILAKSEVQKAFVYSFEESAKTLFENYLDNIEAFCNWTKIRDPLTDEEMEPDERLMRSIEEQIGISENAKKAFREEILIRISAYSRKGKKFEYNNHDRLREAIEKKLFADLKDIVKITTSSKTPDESQLKRINEVSRRLIDEHGYCPICANELLKYVGSLLNR
>NZ_LN831776.1|WP_167345605.1|2612248_2612806_-|hypothetical-protein
MNANVGSGQGVHVNTGGEVGGKHGIGLDAGGSLAHNGAGMHASGHMGAPAYGIHAQGNTHLNTSQGLGINAEAQALGKYGVAAQAKTQLGGGQGAGFQTGAQLGGEYGLQASAEGHLGLSQGAGFNTGLQLGGDNGLGAKAKAQLGGGQGAGLGVAGQVGKYNGQFGFNIGGKDKESKGAEQSED
>NZ_LN831776.1|WP_020433723.1|2613103_2613592_-|DinB-family-protein
MAAKTNEQLVFEFQSLIPYIQSLATLEDADWETPVAAGKWTLKEMLCHITQWDKYFYEEAFAKIQNGQPLTSRHQNFDEFNARAIEYAKSLTTQAAIGQFVLYRTKILESTAGLSDEEFTKIYLDGDGKKFSIRGYLRDFIPHDKHHKRQMEQYLKTMRSSK
>NZ_LN831776.1|WP_046502232.1|2613783_2614677_+|AraC-family-transcriptional-regulator
MNYSKDIERCVEYIEVNIKRNLTAEEIAAEAGYSLYHFSRVFSLCKGMSVMEYVRSRKLSLAAVELFSGKRIIDIALDYGFETQSGFTKAFRKAFGYSPSQYAARMEGFLQMGSKIDIGGYMMNPVIVQKPAFKVAGYGIETNVAEGNYTKDIASFWSHYEGENLESKMYDILNPPKHGEVGLCVPAFDSGNAVYLLGVIVEDFSRVTDEMITVDVPEAEYAVFTTPPVDTSEGKDQEEFVQTIKSTWKYIFEEWFPGSGYVYDEGKLNFEFYDERCHSRVDTVMEIYVPVKKRAGK
>NZ_LN831776.1|WP_020433720.1|2614790_2617175_-|transglutaminase-domain-containing-protein
MKVKQLVMVMLIMCVVLTGCMGGSSEAGPEPSPAPQASAAAETKQPSGNPPPEASQTVYDLKQKYDTDNNPGIMPMYNVDQDMEFIFRFNTDLGSEAIGHTLSVHTDIKALPESKVGTLEDSQLVDGKSVYSIKPLGFGVLASDSLREAGSSSWGNAPVYYIRLNYDLDAATPTPLKQPIIIPFTVKSDLPVPNLQADISPDGRLALVWSEVPGAESYNIYNASHITMENTNEALSGAEQGYADQRPLLIATVPGTSYNDFMKDGRGALGIVDETITSLQNNNVQGEYYVTAVQGDKESKFSASVDTVALSKQLPRTVASEDNLNLKLFKSAGELPKTVPVQYIDGSKAPGTVIYDTDSITIQQSGPTDVQFSIQGTALKGYVQVEKLTDADIASLAAAQSKGANQGYVEPQNNTDYVPAPDVPTIIDNNGNAGESGDNVIDQQKENTRSKVDEGNKQAVPAPTIPADLIHADSALEEYLALNLISGKTEISLQAFPEAQNARTLVDEVEKVIYQNPLILGFRGYSYDYKTLTLHTEFDDPAEVILSKQLKILAEADKVIAAAIKDGMSADEKQMAIYNYLNDNTTYDDAALENAKQQQFKSVDAKFNDSFSTYGILVKKVGVCMSYAHTFQLLSDLVQVPSMVVTGTMDGVNHAWNKVKIGGEWVNVDATNNETNSGLPYLLYNSNDATAANVDYVMDNSSWLDHELSLFQATSNAHDYYVTHGLEADSLEAYKTKLAEQLKQGKTLIVLRVLADTDSAELTQKTAEVIKQYDASKLANAGMIELGSYVAIQL
>NZ_LN831776.1|WP_020433717.1|2617671_2619066_-|SpoVR-family-protein
MPGDEIQALERAIAEITEIASGFGLDFYPMRYEICPADIIYTFGAYGMPTRFGHWSFGKNFHRMKSQYDFGLSKIYELVINSNPCYAFLLDGNSLVQNKLIVAHVLAHCDFFKNNMRFSMSNRDMVESMSATADRIADYSVTYGIDTVESFIDSVLAVQEHIDPSLIQPRKLGKTHLLEAKMKERKDAPPGGSSPANPYEELWDLENSKTAGPEPETAGKRKFPPEPEKDMVWFIQQYSTALEDWQRDIMTMLRDEMLYFWPQMETKIMNEGWASYWHQRIMRELDLTPEETVEYAKLNSSVVQPSRQSLNPYYLGLKIFEDIERRWDRDKMFEVRELDSDISFIRSYLSKQLVNDLDLYVFEKKGPEWKITDKAWENVRDQLVLARVNGGSPYLVVQDADYERNGELLIVHRYESIELDLKYLERTLPHIYALWGRTVHLQTVVEDKKALFTYDGKKVQRRFM
>NZ_LN831776.1|WP_020433715.1|2619535_2620549_-|bifunctional-glycosyltransferase-family-2/GtrA-family-protein
MTILIPAYEPDERLLDLIEQLCDYQLGPIVLVDDGSGPAYQGIFNIAAAFGCTVLTHPVNFGKGLALKTGLRYIREAGLPGYVVCADSDGQHLPHDIKRIAGVLQNQTTPGIVLGSRRFSGTVPLRSRFGNSVTRVVFSLTTGTKIYDTQTGLRGFSPQMLDWLCQIPGERFEYEMNMLLTAHREGYTVTEEFIDTVYLEDNQSSHFRPLADSFRIYLPLLMFSTSSLVSALLDFTLLFLFQRLTHNLFLSVAAARLCSSIFNYSMNRRYVFTGGKMSKLQQSLPKYFALVLLVLLFNYGLLYFYNEKLIIPLAAAKLLTEASIFLFSYWAQRRFVY

Crispr_ID: NZ_LN831776_33

• CRISPR_ID: NZ_LN831776_33
• CRISPR_location: 2627281-2627477
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 3 spacers

Consensus repeat of NZ_LN831776_33

Consensus_repeat	Method
TAAGTGGAAAAAGTAAACTTAAT	CRISPRCasFinder

spacers of NZ_LN831776_33

>33.1|2627304|28|NZ_LN831776|CRISPRCasFinder
CCAGCAAAATATGCAGAAAACCGTGAGT
>33.2|2627355|49|NZ_LN831776|CRISPRCasFinder
TCATTCAGGAATGGAGCATTGGGGCTATAATTGGATATTTGTTAATATG
>33.3|2627427|28|NZ_LN831776|CRISPRCasFinder
TTCTAAAAAAGAACAAAATAGTGAAAAT

CRISPR arrays and Neighbor proteins around NZ_LN831776_33

CRISPR arrays

The CRISPR arrays of NZ_LN831776_33

>merge|NZ_LN831776|33|2627281-2627477|CRISPRCasFinder
TAAGTGGAAAAAGTAAACTTAATCCAGCAAAATATGCAGAAAACCGTGAGTTAGGTGGAAAAAGTAAACTTAATTCATTCAGGAATGGAGCATTGGGGCTATAATTGGATATTTGTTAATATGTAAGTGGATACATTCCACCTAAATTCTAAAAAAGAACAAAATAGTGAAAATTAGGTGGAGAAAATCCACTTAGC

>NZ_LN831776|33|35|2627281-2627477|CRISPRCasFinder
TAAGTGGAAAAAGTAAACTTAAT	CCAGCAAAATATGCAGAAAACCGTGAGT
TAGGTGGAAAAAGTAAACTTAAT	TCATTCAGGAATGGAGCATTGGGGCTATAATTGGATATTTGTTAATATG
TAAGTGGATACATTCCACCTAAA	TTCTAAAAAAGAACAAAATAGTGAAAAT
TAGGTGGAGAAAATCCACTTAGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020433720.1|2614790_2617175_-|transglutaminase-domain-containing-protein	unknown	unknown	gnl|CDD|376628
NZ_LN831776.1|WP_046502253.1|2636530_2644282_+|pullulanase	unknown	unknown	gnl|CDD|273973
NZ_LN831776.1|WP_020433711.1|2621659_2622388_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_LN831776.1|WP_020433717.1|2617671_2619066_-|SpoVR-family-protein	unknown	unknown	gnl|CDD|377285
NZ_LN831776.1|WP_020428210.1|2644720_2646466_-|alpha-glycosidase	unknown	unknown	gnl|CDD|200477
NZ_LN831776.1|WP_039834632.1|2634159_2634822_-|beta-phosphoglucomutase	unknown	unknown	gnl|CDD|213672
NZ_LN831776.1|WP_052741440.1|2625352_2627026_+|PAS-domain-containing-protein	unknown	unknown	gnl|CDD|274362
NZ_LN831776.1|WP_020428212.1|2648731_2650045_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_020428205.1|2631671_2633990_-|glycoside-hydrolase-family-65-protein	unknown	unknown	gnl|CDD|237517
NZ_LN831776.1|WP_020428207.1|2635094_2636132_-|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_LN831776.1|WP_020428211.1|2647283_2648618_+|maltose-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270304
NZ_LN831776.1|WP_046502236.1|2620545_2621517_-|phosphodiester-glycosidase-family-protein	unknown	unknown	gnl|CDD|378342
NZ_LN831776.1|WP_020428197.1|2624372_2625071_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|378937
NZ_LN831776.1|WP_046502240.1|2623462_2624380_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213235
NZ_LN831776.1|WP_020428204.1|2629669_2631358_-|alpha-glucosidase	unknown	unknown	gnl|CDD|200472
NZ_LN831776.1|WP_046502247.1|2628658_2629528_-|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|226231
NZ_LN831776.1|WP_020433715.1|2619535_2620549_-|bifunctional-glycosyltransferase-family-2/GtrA-family-protein	unknown	unknown	gnl|CDD|133022
NZ_LN831776.1|WP_046502232.1|2613783_2614677_+|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|226231
NZ_LN831776.1|WP_020433709.1|2622384_2623320_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|340423
NZ_LN831776.1|WP_046502243.1|2627638_2628484_-|DegV-family-protein	unknown	unknown	gnl|CDD|273257

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020433720.1|2614790_2617175_-|transglutaminase-domain-containing-protein	gnl|CDD|376628	pfam01841, Transglut_core, Transglutaminase-like superfamily. This family includes animal transglutaminases and other bacterial proteins of unknown function. Sequence conservation in this superfamily primarily involves three motifs that centre around conserved cysteine, histidine, and aspartate residues that form the catalytic triad in the structurally characterized transglutaminase, the human blood clotting factor XIIIa'. On the basis of the experimentally demonstrated activity of the Methanobacterium phage pseudomurein endoisopeptidase, it is proposed that many, if not all, microbial homologs of the transglutaminases are proteases and that the eukaryotic transglutaminases have evolved from an ancestral protease.	1.48913e-09
NZ_LN831776.1|WP_046502253.1|2636530_2644282_+|pullulanase	gnl|CDD|273973	TIGR02102, alkaline_amylopullulanase, pullulanase, extracellular, Gram-positive. Pullulan is an unusual, industrially important polysaccharide in which short alpha-1,4 chains (maltotriose) are connected in alpha-1,6 linkages. Enzymes that cleave alpha-1,6 linkages in pullulan and release maltotriose are called pullulanases although pullulan itself may not be the natural substrate. In contrast, a glycogen debranching enzyme such GlgX, homologous to this family, can release glucose at alpha,1-6 linkages from glycogen first subjected to limit degradation by phosphorylase. Characterized members of this family include a surface-located pullulanase from Streptococcus pneumoniae () and an extracellular bifunctional amylase/pullulanase with C-terminal pullulanase activity (.	0
NZ_LN831776.1|WP_020433711.1|2621659_2622388_+|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	1.35808e-87
NZ_LN831776.1|WP_020433717.1|2617671_2619066_-|SpoVR-family-protein	gnl|CDD|377285	pfam04293, SpoVR, SpoVR like protein. Bacillus subtilis stage V sporulation protein R is involved in spore cortex formation. Little is known about cortex biosynthesis, except that it depends on several sigma E controlled genes, including spoVR.	0
NZ_LN831776.1|WP_020428210.1|2644720_2646466_-|alpha-glycosidase	gnl|CDD|200477	cd11338, AmyAc_CMD, Alpha amylase catalytic domain found in cyclomaltodextrinases and related proteins. Cyclomaltodextrinase (CDase; EC3.2.1.54), neopullulanase (NPase; EC 3.2.1.135), and maltogenic amylase (MA; EC 3.2.1.133) catalyze the hydrolysis of alpha-(1,4) glycosidic linkages on a number of substrates including cyclomaltodextrins (CDs), pullulan, and starch. These enzymes hydrolyze CDs and starch to maltose and pullulan to panose by cleavage of alpha-1,4 glycosidic bonds whereas alpha-amylases essentially lack activity on CDs and pullulan. They also catalyze transglycosylation of oligosaccharides to the C3-, C4- or C6-hydroxyl groups of various acceptor sugar molecules. Since these proteins are nearly indistinguishable from each other, they are referred to as cyclomaltodextrinases (CMDs). The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues (Asp, Glu and Asp) performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase.	0
NZ_LN831776.1|WP_039834632.1|2634159_2634822_-|beta-phosphoglucomutase	gnl|CDD|213672	TIGR01990, bPGM, beta-phosphoglucomutase. This model represents the beta-phosphoglucomutase enzyme which catalyzes the interconverison of beta-D-glucose-1-phosphate and beta-D-glucose-6-phosphate. The 6-phosphate is capable of non-enzymatic anomerization (alpha <-> beta) while the 1-phosphate is not. A separate enzyme is responsible for the isomerization of the alpha anomers. Beta-D-glucose-1-phosphate results from the phosphorylysis of maltose (2.4.1.8), trehalose (2.4.1.64) or trehalose-6-phosphate (2.4.1.216). Alternatively, these reactions can be run in the synthetic direction to create the disaccharides. All sequenced genomes which contain a member of this family also appear to contain at least one putative maltose or trehalose phosphorylase. Three species, Lactococcus, Enterococcus and Neisseria appear to contain a pair of paralogous beta-PGM's. Beta-phosphoglucomutase is a member of the haloacid dehalogenase superfamily of hydrolase enzymes. These enzymes are characterized by a series of three catalytic motifs positioned within an alpha-beta (Rossman) fold. beta-PGM contains an inserted alpha helical domain in between the first and second conserved motifs and thus is a member of subfamily IA of the superfamily. The third catalytic motif comes in three variants, the third of which, containing a conserved DD or ED, is the only one found here as well as in several other related enzymes (TIGR01509). The enzyme from L. lactis has been extensively characterized including a remarkable crystal structure which traps the pentacoordinate transition state. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	1.30737e-77
NZ_LN831776.1|WP_052741440.1|2625352_2627026_+|PAS-domain-containing-protein	gnl|CDD|274362	TIGR02956, sensor_protein_TorS, TMAO reductase sytem sensor TorS. This protein, TorS, is part of a regulatory system for the torCAD operon that encodes the pterin molybdenum cofactor-containing enzyme trimethylamine-N-oxide (TMAO) reductase (TorA), a cognate chaperone (TorD), and a penta-haem cytochrome (TorC). TorS works together with the inducer-binding protein TorT and the response regulator TorR. TorS contains histidine kinase ATPase (pfam02518), HAMP (pfam00672), phosphoacceptor (pfam00512), and phosphotransfer (pfam01627) domains and a response regulator receiver domain (pfam00072). [Signal transduction, Two-component systems].	2.41653e-81
NZ_LN831776.1|WP_020428212.1|2648731_2650045_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	3.04194e-68
NZ_LN831776.1|WP_020428205.1|2631671_2633990_-|glycoside-hydrolase-family-65-protein	gnl|CDD|237517	PRK13807, PRK13807, maltose phosphorylase; Provisional.	0
NZ_LN831776.1|WP_020428207.1|2635094_2636132_-|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	4.20211e-123
NZ_LN831776.1|WP_020428211.1|2647283_2648618_+|maltose-ABC-transporter-substrate-binding-protein	gnl|CDD|270304	cd13586, PBP2_Maltose_binding_like, The periplasmic-binding component of ABC transport systems specific for maltose and related polysaccharides; possess type 2 periplasmic binding fold. This subfamily represents the periplasmic binding component of ABC transport systems involved in uptake of polysaccharides including maltose, maltodextrin, and cyclodextrin. Members of this family belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	4.75893e-126
NZ_LN831776.1|WP_046502236.1|2620545_2621517_-|phosphodiester-glycosidase-family-protein	gnl|CDD|378342	pfam09992, NAGPA, Phosphodiester glycosidase. This is a family conserved from bacteria to humans. The structure of a member from Bacteroides has been crystallized and modelled onto the luminal region of the human member of the family, the transmembrane glycoprotein N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase. There is some conservation of potentially functional residues, implying that in the bacterial members this family acts in some way as a phosphodiester glycosidase. The human protein is also present, so the eukaryotic members are likely to be catalyzing the second step in the formation of the mannose 6-phosphate targeting signal on lysosomal enzyme oligosaccharides.	1.75716e-44
NZ_LN831776.1|WP_020428197.1|2624372_2625071_+|ABC-transporter-permease-subunit	gnl|CDD|378937	pfam12730, ABC2_membrane_4, ABC-2 family transporter protein. This family is related to the ABC-2 membrane transporter family pfam01061.	1.02587e-05
NZ_LN831776.1|WP_046502240.1|2623462_2624380_+|ABC-transporter-ATP-binding-protein	gnl|CDD|213235	cd03268, ABC_BcrA_bacitracin_resist, ATP-binding cassette domain of the bacitracin-resistance transporter. The BcrA subfamily represents ABC transporters involved in peptide antibiotic resistance. Bacitracin is a dodecapeptide antibiotic produced by B. licheniformis and B. subtilis. The synthesis of bacitracin is non-ribosomally catalyzed by a multi-enzyme complex BcrABC. Bacitracin has potent antibiotic activity against gram-positive bacteria. The inhibition of peptidoglycan biosynthesis is the best characterized bacterial effect of bacitracin. The bacitracin resistance of B. licheniformis is mediated by the ABC transporter Bcr which is composed of two identical BcrA ATP-binding subunits and one each of the integral membrane proteins, BcrB and BcrC. B. subtilis cells carrying bcr genes on high-copy number plasmids develop collateral detergent sensitivity, a similar phenomenon in human cells with overexpressed multi-drug resistance P-glycoprotein.	3.82377e-97
NZ_LN831776.1|WP_020428204.1|2629669_2631358_-|alpha-glucosidase	gnl|CDD|200472	cd11333, AmyAc_SI_OligoGlu_DGase, Alpha amylase catalytic domain found in Sucrose isomerases, oligo-1,6-glucosidase (also called isomaltase; sucrase-isomaltase; alpha-limit dextrinase), dextran glucosidase (also called glucan 1,6-alpha-glucosidase), and related proteins. The sucrose isomerases (SIs) Isomaltulose synthase (EC 5.4.99.11) and Trehalose synthase (EC 5.4.99.16) catalyze the isomerization of sucrose and maltose to produce isomaltulose and trehalulose, respectively. Oligo-1,6-glucosidase (EC 3.2.1.10) hydrolyzes the alpha-1,6-glucosidic linkage of isomaltooligosaccharides, pannose, and dextran. Unlike alpha-1,4-glucosidases (EC 3.2.1.20), it fails to hydrolyze the alpha-1,4-glucosidic bonds of maltosaccharides. Dextran glucosidase (DGase, EC 3.2.1.70) hydrolyzes alpha-1,6-glucosidic linkages at the non-reducing end of panose, isomaltooligosaccharides and dextran to produce alpha-glucose.The common reaction chemistry of the alpha-amylase family enzymes is based on a two-step acid catalytic mechanism that requires two critical carboxylates: one acting as a general acid/base (Glu) and the other as a nucleophile (Asp). Both hydrolysis and transglycosylation proceed via the nucleophilic substitution reaction between the anomeric carbon, C1 and a nucleophile. Both enzymes contain the three catalytic residues (Asp, Glu and Asp) common to the alpha-amylase family as well as two histidine residues which are predicted to be critical to binding the glucose residue adjacent to the scissile bond in the substrates. The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase.	0
NZ_LN831776.1|WP_046502247.1|2628658_2629528_-|AraC-family-transcriptional-regulator	gnl|CDD|226231	COG3708, COG3708, Uncharacterized protein conserved in bacteria [Function unknown].	3.04718e-39
NZ_LN831776.1|WP_020433715.1|2619535_2620549_-|bifunctional-glycosyltransferase-family-2/GtrA-family-protein	gnl|CDD|133022	cd04179, DPM_DPG-synthase_like, DPM_DPG-synthase_like is a member of the Glycosyltransferase 2 superfamily. DPM1 is the catalytic subunit of eukaryotic dolichol-phosphate mannose (DPM) synthase. DPM synthase is required for synthesis of the glycosylphosphatidylinositol (GPI) anchor, N-glycan precursor, protein O-mannose, and C-mannose. In higher eukaryotes,the enzyme has three subunits, DPM1, DPM2 and DPM3. DPM is synthesized from dolichol phosphate and GDP-Man on the cytosolic surface of the ER membrane by DPM synthase and then is flipped onto the luminal side and used as a donor substrate. In lower eukaryotes, such as Saccharomyces cerevisiae and Trypanosoma brucei, DPM synthase consists of a single component (Dpm1p and TbDpm1, respectively) that possesses one predicted transmembrane region near the C terminus for anchoring to the ER membrane. In contrast, the Dpm1 homologues of higher eukaryotes, namely fission yeast, fungi, and animals, have no transmembrane region, suggesting the existence of adapter molecules for membrane anchoring. This family also includes bacteria and archaea DPM1_like enzymes. However, the enzyme structure and mechanism of function are not well understood. The UDP-glucose:dolichyl-phosphate glucosyltransferase (DPG_synthase) is a transmembrane-bound enzyme of the endoplasmic reticulum involved in protein N-linked glycosylation. This enzyme catalyzes the transfer of glucose from UDP-glucose to dolichyl phosphate. This protein family belongs to Glycosyltransferase 2 superfamily.	6.23937e-33
NZ_LN831776.1|WP_046502232.1|2613783_2614677_+|AraC-family-transcriptional-regulator	gnl|CDD|226231	COG3708, COG3708, Uncharacterized protein conserved in bacteria [Function unknown].	1.14341e-32
NZ_LN831776.1|WP_020433709.1|2622384_2623320_+|sensor-histidine-kinase	gnl|CDD|340423	cd16947, HATPase_YcbM-like, Histidine kinase-like ATPase domain of two-component sensor histidine kinases similar to Bacillus subtilis YcbM. This family includes the histidine kinase-like ATPase (HATPase) domains of various two-component sensor histidine kinase (HKs) such as Bacillus subtilis YcbM, a HK of the two-component system YcbM-YcbL. Proteins having this HATPase domain also contain a histidine kinase dimerization and phosphoacceptor domain (HisKA).	4.17892e-57
NZ_LN831776.1|WP_046502243.1|2627638_2628484_-|DegV-family-protein	gnl|CDD|273257	TIGR00762, DegV, EDD domain protein, DegV family. This family of proteins is related to DegV of Bacillus subtilis and includes paralogous sets in several species (B. subtilis, Deinococcus radiodurans, Mycoplasma pneumoniae) that are closer in percent identity to each than to most homologs from other species. This suggests both recent paralogy and diversity of function. DegV itself is encoded immediately downstream of DegU, a transcriptional regulator of degradation, but is itself uncharacterized. Crystallography suggested a lipid-binding site, while comparison of the crystal structure to dihydroxyacetone kinase and to a mannose transporter EIIA domain suggests a conserved domain, EDD, with phosphotransferase activity. [Unknown function, General].	3.36406e-111

Protein sequences

>NZ_LN831776.1|WP_052741440.1|2625352_2627026_+|PAS-domain-containing-protein
MPIKWSSILDRVLSGEGAYKALYDHHPDLIIVLDRQGYYVESNRAFEAVAGAKAKAEAELHEPLSCSRPQPPGEEHFAAALGGIGSRVELPVEEGSGSSPAAITYVPIQAEEGIAGVFAIIHYGQSCGLPLEVEKWLGSLITREEPPPEWTDDRAPGHEEMLAAIGAAAEQQQAELVPGMSEDKHLGLILNSVAAGIFGLDTQGRIFFINREGADMLGYAPAELIGRTFAGQVHHIHGDGSRYQKIESPIAQTLQDGRTRSKGDEIFWRKDGTSFFVSCRIAPLMHKGMICGVVGSFSDITNEREILRAKETAEQAAQAKADFLAMMSHEIRTPMNGMIGMADLLLETELEEEQRTYAEILRSSSHSLLKILNDILDFSKMEAGKMPLLSEKFDLREMMESVIDLFTPKAEEKKLALRWWADTSVPSMVTTDPSRLRQIIVNLVGNALKFTERGSVTLSVKNIQLPASPEYLLEFSVRDTGVGIADSKLNLLFQSFSQLHPFINRKYGGTGLGLAICKQLVELMGGTIFVESEEGRGSTFRFMLPFIKEEMEADITP
>NZ_LN831776.1|WP_020428197.1|2624372_2625071_+|ABC-transporter-permease-subunit
MLKLIQLEIRKNKLTGMLKGVAIAVLMILGFMLLLTYVDAEDGSGRGEFKTYADMFEGLYVIVKVTFVVFASVVLSKLVIDEYKNNTITLLFMYPISRKKLLGAKIIIVFLFTLLSVFISDILISALLIGINSFTHVIPEQLDWAGIPGELLRMGMDAIFAAGIGLIPLYIGMRKKSVPATIVTAVLFVSVSSSDFGGFRMSNLVGISIFLSLVGVAIAYLSIRNIEQKDIA
>NZ_LN831776.1|WP_046502240.1|2623462_2624380_+|ABC-transporter-ATP-binding-protein
MTTILRTWDLTKEYQGKEAVSGVNMSVKQGEIYGFLGPNGAGKTTVMKMITNLVKPTAGNIEFFGESITDHSYEMLKRMGCIIEYPVFYDKLTARENLQLHGEYMGYYDARAMEEALELVKLKGVDKKPVKQFSLGMKQRLGIARAVMTKPELLILDEPINGLDPMGIKEMREVFRMLSREYGMTLLISSHLLGEVEQVADTIGVIRDGILLEEVAMDMIRSQNTQYIELITGESSKAVYVLEHKLGLTNFKVLDPRTIRIYDAVQQLELNKALVEAGVELESLSKKNHSLEDHFVELMGGEGIA
>NZ_LN831776.1|WP_020433709.1|2622384_2623320_+|sensor-histidine-kinase
MIAFWSVAVLLLLLVILWQYLRLREHSRRLEYIHTKLTDIMDRDSHERLLLFNSDPHLQKLLTDLNRLLDVNHRGAVELAKLEKSMRSMLANISHDLKTPLTVVLGYIETVLQDQTMPMEEQEKILRMIHAKAEEVIRLMNSFFDLAKLESGDKDIPLSRVELGEVCRRNILSFYEILNAKGSEVDIELPDEALYIMGNEEALDRVLSNLLSNAIKYGDAGGVLGLRLYSDGDQVCIEVWDRGKGITEGDQDKVFERLYTLEDSRNRDYQGSGLGLTITKRLTEQMNGSITLRSKPHVKTAFTLSFRRQTF
>NZ_LN831776.1|WP_020433711.1|2621659_2622388_+|response-regulator-transcription-factor
MPQRVLLIEDDEAISEMVRSYLVKEGYEVETAFDGDAAERLFHHGGAYDLVLLDLMLPKRSGSDVLQTIRRDSLVPVLIMSAKDSDVDKALGLGFGADDYITKPFSMIELAARVKAAIRRAGYAAVGSSGQEAAPAQEKANIISLRGLTVDLDNFSVLKNGEEVKLTAKEFQILGMFASSPGRVYTKAQIYKSVWEDDYYGDENVINVHMRRLREKIEDDPSKPEYIKTLWGIGYKLGDVLE
>NZ_LN831776.1|WP_046502236.1|2620545_2621517_-|phosphodiester-glycosidase-family-protein
MKNLRTRQAWSFKRKLLVVMIVVLLGLGTVIYSLADRYLIEHVEVAVADDAAAAGSSENAAATAAEVNAAADDWNYSSDDIQIRIDQVQTGSGPDQITYFVADVVLKDTSSLRAAFADNSFGTNITEDTSEIASSNNAIFAINGDYYGFRNDGVIIRNGTLYRDDPVRDAMALFKDGTMQTYSEEEVSSSDLLAQGAANTLSFGPILIQDGKIASDFSNVKIDTNFGNRSIQNANPRTAVGMIAPNHYVFVVVDGRSEGYSRGMTLTELANVMSDLGATEAYNLDGGGSSTMYFMGRVVNNPQGKNQERGVSDILYIKEGATS
>NZ_LN831776.1|WP_020433715.1|2619535_2620549_-|bifunctional-glycosyltransferase-family-2/GtrA-family-protein
MTILIPAYEPDERLLDLIEQLCDYQLGPIVLVDDGSGPAYQGIFNIAAAFGCTVLTHPVNFGKGLALKTGLRYIREAGLPGYVVCADSDGQHLPHDIKRIAGVLQNQTTPGIVLGSRRFSGTVPLRSRFGNSVTRVVFSLTTGTKIYDTQTGLRGFSPQMLDWLCQIPGERFEYEMNMLLTAHREGYTVTEEFIDTVYLEDNQSSHFRPLADSFRIYLPLLMFSTSSLVSALLDFTLLFLFQRLTHNLFLSVAAARLCSSIFNYSMNRRYVFTGGKMSKLQQSLPKYFALVLLVLLFNYGLLYFYNEKLIIPLAAAKLLTEASIFLFSYWAQRRFVY
>NZ_LN831776.1|WP_020433717.1|2617671_2619066_-|SpoVR-family-protein
MPGDEIQALERAIAEITEIASGFGLDFYPMRYEICPADIIYTFGAYGMPTRFGHWSFGKNFHRMKSQYDFGLSKIYELVINSNPCYAFLLDGNSLVQNKLIVAHVLAHCDFFKNNMRFSMSNRDMVESMSATADRIADYSVTYGIDTVESFIDSVLAVQEHIDPSLIQPRKLGKTHLLEAKMKERKDAPPGGSSPANPYEELWDLENSKTAGPEPETAGKRKFPPEPEKDMVWFIQQYSTALEDWQRDIMTMLRDEMLYFWPQMETKIMNEGWASYWHQRIMRELDLTPEETVEYAKLNSSVVQPSRQSLNPYYLGLKIFEDIERRWDRDKMFEVRELDSDISFIRSYLSKQLVNDLDLYVFEKKGPEWKITDKAWENVRDQLVLARVNGGSPYLVVQDADYERNGELLIVHRYESIELDLKYLERTLPHIYALWGRTVHLQTVVEDKKALFTYDGKKVQRRFM
>NZ_LN831776.1|WP_020433720.1|2614790_2617175_-|transglutaminase-domain-containing-protein
MKVKQLVMVMLIMCVVLTGCMGGSSEAGPEPSPAPQASAAAETKQPSGNPPPEASQTVYDLKQKYDTDNNPGIMPMYNVDQDMEFIFRFNTDLGSEAIGHTLSVHTDIKALPESKVGTLEDSQLVDGKSVYSIKPLGFGVLASDSLREAGSSSWGNAPVYYIRLNYDLDAATPTPLKQPIIIPFTVKSDLPVPNLQADISPDGRLALVWSEVPGAESYNIYNASHITMENTNEALSGAEQGYADQRPLLIATVPGTSYNDFMKDGRGALGIVDETITSLQNNNVQGEYYVTAVQGDKESKFSASVDTVALSKQLPRTVASEDNLNLKLFKSAGELPKTVPVQYIDGSKAPGTVIYDTDSITIQQSGPTDVQFSIQGTALKGYVQVEKLTDADIASLAAAQSKGANQGYVEPQNNTDYVPAPDVPTIIDNNGNAGESGDNVIDQQKENTRSKVDEGNKQAVPAPTIPADLIHADSALEEYLALNLISGKTEISLQAFPEAQNARTLVDEVEKVIYQNPLILGFRGYSYDYKTLTLHTEFDDPAEVILSKQLKILAEADKVIAAAIKDGMSADEKQMAIYNYLNDNTTYDDAALENAKQQQFKSVDAKFNDSFSTYGILVKKVGVCMSYAHTFQLLSDLVQVPSMVVTGTMDGVNHAWNKVKIGGEWVNVDATNNETNSGLPYLLYNSNDATAANVDYVMDNSSWLDHELSLFQATSNAHDYYVTHGLEADSLEAYKTKLAEQLKQGKTLIVLRVLADTDSAELTQKTAEVIKQYDASKLANAGMIELGSYVAIQL
>NZ_LN831776.1|WP_046502232.1|2613783_2614677_+|AraC-family-transcriptional-regulator
MNYSKDIERCVEYIEVNIKRNLTAEEIAAEAGYSLYHFSRVFSLCKGMSVMEYVRSRKLSLAAVELFSGKRIIDIALDYGFETQSGFTKAFRKAFGYSPSQYAARMEGFLQMGSKIDIGGYMMNPVIVQKPAFKVAGYGIETNVAEGNYTKDIASFWSHYEGENLESKMYDILNPPKHGEVGLCVPAFDSGNAVYLLGVIVEDFSRVTDEMITVDVPEAEYAVFTTPPVDTSEGKDQEEFVQTIKSTWKYIFEEWFPGSGYVYDEGKLNFEFYDERCHSRVDTVMEIYVPVKKRAGK
>NZ_LN831776.1|WP_046502243.1|2627638_2628484_-|DegV-family-protein
MSIVKIFSDSTSDLPQGWKETYDIGIIPLYVVFEDATYRDGVDITPEEVYRRVAAQGALPKTAAPSPADFMAAFEPVIRSGGDVVYISLSSALSSTYQNALLAAVEFPEGRVHVVDSETLCGGIALLVMKAARAAARGQSAPEIAAMVKECRSQVQTEFVVDTLDYLYMGGRCSGMQNFIGSLLKIRPVLRLIDGAIVPVSKIRGKKEKAIEQMLHHALEHAGTIDKELIIVAHTLAEEDAKYLEKALREQTGSGEIAIIHAGCVIGSHCGPGTVGLMYMH
>NZ_LN831776.1|WP_046502247.1|2628658_2629528_-|AraC-family-transcriptional-regulator
MADLEWLIRMKDALDFMESRMTEPLRIEDVAKVAHVSPFHFQRMFAMLTGVTVADYIRKRRLTLAAQELAISKIRVLDVALKYGYESPEAFAKAFRKAHGLTPSAAREPGVQLKAFPRLTFHLSLKGDQEMEYKIVEKPAFTVIGKSMEVTTRDGENLRRIPEFWNECNADGTSDELIEIGKGKDWLGICMSMDMEKELLSYWIGVEGTPETDPQGYETAVVPAASWAVFTSAGPMPHAIQKVWQRIFQEWFPGTGYEHTGGPEFELYPPGDTGAEDYVCEVWIPVQKK
>NZ_LN831776.1|WP_020428204.1|2629669_2631358_-|alpha-glucosidase
MNRTFWKEAVVYQIYPRSFQDSNGDGIGDLQGIISRLDYLHKLGVDVVWLSPVYKSPNDDNGYDISDYEDIMDEFGTLDDWEELLDGLHARGIKLMMDLVINHSSDEHAWFVESRSSKDNPYRDYYIWRPGGPDGELPNNWSSIFSGPAWELDEKTGEYYLHLFSRKQPDLNWENPELREALYKMMAFWLDKGVDGLRMDVINMISKVEGLPSAHYEGLAPGELAGGGEYYMNGPRVHEYLQEMNRKVLSKYNVMTVGETPGATVEDAILYTAEDRNELQMVFQFEHMDVDSGPGGKWNVTPWNLTKLRDILHKWQVGLADRGWNSLYLNNHDQPRMVSRFGNDREYRVISAKMLATLLHTLKGTPYIYQGEEIGMTNVQFPQLEDYKDIEIHNMYKEKVTVGGGDHEAILKAIHIKGRDNARTPMQWDSSPNAGFTEGTPWLKLNPRYEEINVEQALADPDSVFYYYQKLIRLRKNHPVMVYGDYELLLPEHEYIYAYTRTLEGERWLILLNFCDTPQTVDLLEELNAVTETIISNYPEEQPAMDRETLRPYEARVCRLGG
>NZ_LN831776.1|WP_020428205.1|2631671_2633990_-|glycoside-hydrolase-family-65-protein
MKQYLKIDEWSIIEESFDPQTQEISESVFSIGNGYMGGRANFEEQYSGHSLQGSYMAGVYYPDKTRVGWWKNGYPEYFAKVLNSTNWIGINIDIDGTPLDLAACTVTDFRRELNMKEGTLSRSFTAVTADGKEVRVDSLRIVSMARREIGAIRYSVSPVNFAGELTITPYLDGDIKNKDANYDEKFWNEVEKKSGPDGGHLTLKTKKLDFHVTSAYLFDILLNGEKLTREAVTLEEEKYVASRVSFPVKSGDQVVIYKYAANVTSRNHGLGQLVEAAETALHSAREAGFAALLTEQAEAWKDKWKESDIIIEGDVSAQQAIRFNIFQLNQTYTGEDDRLNIGPKGFTGEKYGGSTYWDTEAYCVPFYLSTADSSIARNLLIYRYKHLEKAKENARKLGFKKGALYPMVTMNGEECHNEWEITFEEIHRNGAIAYAIYNYVNYTGDQAYLGQYGLEVLVEISRFWEERVHYVPHKDKYVMLGVTGPNEYENNVNNNWYTNRMASWTMEYTLEALAYLQENEAARYAELVDKLELAEDETAKWNDIIAKMYYAADEELGIFLQQDGFLDKEIIQVKDVLPENLPLNQKWSWDRILRSCFIKQADVLQGLYFLGDRYDLETKKRNFDFYEPITVHESSLSPCIHAILACELGYKEKAYEMYLRTSRLDLDNYNNDTEDGCHTTSMAGTWMSIVHGFGGLRVQADRLILNPSNPGHWTAYSFKIMFRGSRLKVSVTDVQVTVVNETDIPASITIYGKDYTVNGLSSVTAEGSSVTV
>NZ_LN831776.1|WP_039834632.1|2634159_2634822_-|beta-phosphoglucomutase
MSEIKACLFDLDGVLVDTAKYHYIAWRELAEQLGFVFTEKDNERLKGVSRTASLNILLEIGGLTLDETRKAELAEQKNNRYVEYIAKMDSSEILPGALDFLKECRAQGIKTALGSASKNAMLILNNTGLTPYFDAIIDGTHTSAAKPDPEVFLLGARATYTEPGQCVVFEDAEAGITAAIRAGMRSVGIGSPETLGAANLVVPSLAHISVAALRESFAGV
>NZ_LN831776.1|WP_020428207.1|2635094_2636132_-|LacI-family-DNA-binding-transcriptional-regulator
MTVTIKDVAKKAGVSPSTVSRVLSGHPRISLETSRKVKEIMEEMGYTPNMMAKSLVSKTTNSICIILPKPAEELFSNLFFMELIRGIVTQSSRSGYDVLISSGANEKEELESVSRLLKGRRVDGVILLYSRKDDAVIDFLESGGYPFVLVGRSDRYEDILSVDNDNIMASFDATNHLISMGHERIGFVSGPPNLIVSRDRLEGYRKAMANSGLEMRAEWIVEGEFLQDSGYRAMSFFMNLPNRPTALVAVDDMVSFGVLRGLNELNYKVPEDLAIVSFNNIPLSELSSPPISSIDIGIYHLGYTASQVLIQSIQKPDNHDGYTNRFVIPHRLIVRESSMHSPVKK
>NZ_LN831776.1|WP_046502253.1|2636530_2644282_+|pullulanase
MKWALWGKKAFSVSMIVVLVCSYFSFYPGSVVNAAASKVVLVGSLQSELSTEAEPAGDWDPAASVTEMTYVDNGLYKFTGRLPAGVYEYKIALNGSWEESYGYGNYTNSAGVNKDGNIQISLAAETSVTFYYNDLTKKIADSTYYTPVEADKLPRLTGTLQTELGDARDSSPADAKATLSDPDLDGVYERSAELPAGEYAYRVYVPGDTPDTDMFYPGGEQKLNLPAASKVTFTYNAQDHGVKASFTVPNAPGAAVPVPEGQLRIHYSRTAGDYAGLGLWMWDDVAAPSAGWPSGATPFPEGQTDAYGAYVDVPLKAGAKKVSFLVVNRSTEAKDGGNKLFMINTPQTNEVWVKEGSDTVTPYEPVVLPADTVRVHYARADSNWSQYGLWLWDEVASEPVTWPGDALPFLAEHTDAYGAYVDVPLKTDAQKIGFLVVNRSSGDKDGGDKTFRLLDRYNQLWIKQGDDHVYVSPFGEQPVSLVSAEILSTRKILLTFTLTDGLDAAGLKSLITVTDKEGTPVPVNAAAIKSTTSVEVDTAAFALEKAPLSVAYSGKNVSASAGWRMIDEMYNYTGDDLGATYHPADQSATLKLWAPMASSVVANVYSKTDAAQQVGQVSLTLGDKGVWSAELKPSDLSKAAAAEDVRGYYYQYEVTNNGVTKPVLDPYAKSMAVFTVDSTGAAGPDGDTVGKAAIVDLSGTNPPDYRAGDIPGYEKREDAVIYEVHVRDFTSDVSIESELGGERWGSYAAFAKKLDYIKSLGITHIQLMPVMAWYNGDETRMTHRESGYSTQNNEYNWGYDPHSYFSPDGAYSQQPADPEERIKELKGLIDAVHEAGMGVILDVVYTHMAKKDFLDDIVPNYYAFQDANGNFVGGFGNNLATSHKMAEKLMVDSVKYWFSEYKIDGMRWDMMGDATYDAVQAAYDAAEAINPKALFIGEGWKTFAGDASDPALAGKGADQAWMDKTDSVGVFSDEFRNELKSGYGSEGEPRFITGGARSIAAIFNNITARPSNIPADDPGDVVPYIEAHDNLTLHDVIAQTIKKDPSIPANELEIQQRIRLGNLLEMTSQGTAFIQAGQEYGRTKQWKAAGVPEQKYTEMKDANGQSFGYFIHDSYDSSDAVNMFDWAKATDEVNYPVQNTTRAYTSGLIQLRKSTDAFRLGDKSLVDTNVNLITAPEIKATDLVIGYKNKATDGTGLYYVFMNGDDAARTLTLSEDLTGGQVLVDNDQAGVTAIPAESQSGFTLTSTSITLDPLTAVVIRKDAAAAVLASLGTDSTGYALQAGSTHQTAVTAKYDDGSARTVTNAAAYISSNPAVAAVTSKGLVKGVKPGTATITITYGGLSAKVNVEVTKEPVDTKRYVQITYVRDDKDYADWNLWVWNTGVKNDQIDFTTFKDGKASVLIEVAPNATSVGFVLRKGTDWNTGKQDYPDDRVIPLTAGEAFTKVNVTSMVKELDIKPVINGPVMKDGTITFRYRDDALFRTDQQETISGVKVKVNGKEYPMAYEAAEEWFSYKLQDVQEGTYKYSFLVTKDGVTEELTDPKNTVNGESVVVYHIPKVAITAEVQPEAINSNENAVVTVKAASEEQVSYVDGYMDLSALGGPEAVKLDTELLQQTVAVKNSVPAGLKSIPITLLDQYGNTHKGTAQIEVKARTYTGGQLDFDWDEARIYFALTDRFKDGDATNNADVDTTHPEAYHGGDFRGMIDSLDYLQKLGINTLWITPVVDNIDFNKGADFGGTQYGYHGYWAKDFTQLDEHLGDMATFKELIEKAHDKGIKIMVDVVLNHAGYGLKAEDNYPGVTAEDKARFDGMLRKDGVSADTDPIKGELAGLPDFKTEDPAVRQTLIGWQTGWLDNARTERGDTIDYFRVDTVKHVDSTTWKAFKNALTAIDPAFKLTGEYFGGTLDNDGGNLHSGQMDGLLDFGFKNAAKDFTDGKISAVDTYLQHREAQMDNTGMMAQFLSSHDENGFLSNYVDGDKSKLKIAAALQITAKGQPVIYYGEELGRSGANSGDLSKGEFSENRGDMPWDQLSAEQGLHDHYQKLLNIRAKYSQIYSKGIRTKLAGSDELGYLAFDKQYDGANIVTAINTKAEAVSVSLPVPFAAQAAVVDEYSGKTYTVSGDQKVRVELPGRGDGGTVILAVVPKVTPTPTPTATASPTPTATPTPTPTATPTPTPEPGNGSGWNPVVTATATPAADTQLINGDSLKNGKDGKVTVELASGKQAALLPLQAAAMLGTNDLVLTMSGLSITLPVQVLRTVQGTLTGADAEGAQILLGAAPLASNAASALVAGLSKDNMSVTAASELYEFRLEVIRKDGKRVPVTSFAEPVKLAFQLKGNPDKALLGVYYLGDNSSLQYAGGSQQGDIITAGVTHFSTYAALVINKAYSDVPAAYWAETAIKSLSAKQVITGVTASEFKPGNPVTRAEFTALLVRALSLQTEGQAASQDVRAGEQSGFTDVKAGEQNGFTDVKEDAWYASYVSAAVRQGVVTGRSNGLFAPDAVISREEMAVMIIRALELKQGKKLEPANGGLRFADASSISSWAAEYVSAAAEQGLLQGRAANKFAPEAWMTRAEAAQVIYRLLGK
>NZ_LN831776.1|WP_020428210.1|2644720_2646466_-|alpha-glycosidase
MLLEAVYHRPRLNWSYAYDHETIHLRLRAKKGDLTEVFAWAGDKYAWDATKELIPMTLFTSDAMFDYWECSSVPPYRRLKYGFLLQKGHERIWMTESEFVTERPANPNRLFEFPYINRGDVFTPPAWVKDAVFYQIFPERFANGDPSRNPADVQPWGETPTPENFFGGDLQGVIDHLDHLSELGITGIYFTPIFTATTNHKYDTEDYMSVDPHFGDVETLKKLVAACHERGIRVLLDAVFNHSGRTFAPFVDVLEKGEASPFKDWFHVREFPLQVVDNIPTYDAFAFEPLMPKLNTENPAVKEYLLKVAEYWITEVGIDGWRLDVANEVDFEFWRDFRKVVKRANPDAYILGEIWHESSPWLEGDKFDAVMNYPFTDAVLDFFVYGTLDAEGFANAIGKQLSRYPLQASEVAFNLLDSHDTPRLLTLAGGDKNKQKLAALFQFTFMGTPCIYYGDEIGMDGEGDPGCRKCMEWNPEHQDLDLFSFYRKLIEIRSSHPELRTGTFTFLEAGPQGSKLAYERRLGDNLILVLVNTEETAQTFSLDVEDRNWENLFTGDTLRAERSKLSIKLPAYGYAVLKALL
>NZ_LN831776.1|WP_020428211.1|2647283_2648618_+|maltose-ABC-transporter-substrate-binding-protein
MELKKLMVLTAAFSMAVSITACSSNNNGNNGENAAATTAPADNATATDAANSGNATAAGDIKPEEGASLLVWESKEERVFAEEIAKQFTAKYNVPVKIEEVAPPDQVGKLTQDGPSGLAADVVLIPHDNLGKAASASLLLPNDIFAEQTKAANTEASIVGSSYDGELYGYPRAAETYALYYNKSLVKEAPKTFDDVIAFGKTFTDKAKNKYGIMWEVGNMYFGYPFIATTGGYLFGKDGTDKDDIGLNNEGAIEGLKTFVKLKEVLPIKSGDINSDIKRSLFSSGDVAMDMTGPWELAAYKQALGDKLGVAPVPTVDGKTAITFSGIKIFAVNAYTQYPNAAKLYAEFASSKESQLELNKLVGSIPTNNEALKDPQITGDPYISAFAEQAKNSQPMPSIPEMGNVWSPVNAALPEIWDNNADPKAAMDKAVQQIKDLNNGAAAK
>NZ_LN831776.1|WP_020428212.1|2648731_2650045_+|sugar-ABC-transporter-permease
MQRHRTRAAILSTIFMGLGQIYNRQFIKGLIFIAVEAGALVYFIANLGEAFWGITTLGDSPSHLEKVKGIAKMVPGDHSIVILIQSLITLMFFVLFLIAWYMNIRDAHKTGEERETGRPSNTFKQSVRYILDYKFAQSFLLLPGIGILFFTIMPIIFMIMLAFTNYAAPDHIPPAKLVDWVGFETFRNLLVLKSWSHTFYGVLTWTIIWAVLSTITTYFGGMLVALLINQKGIRFKGLWRLILIVPYAIPQMISLLLMRNLFNGQFGPINQYLGYFGLGGLPWLTDPFWAKVTVIMVNMWVGIPVSMLLIMGVLTTIPRDMYEAAEVDGATNYQKFRIVTLPMILFSTAPTLIMQFAGNINNFNAIYLLTQGNPVNGNYQYAGSTDLLVTWLYKLTLDQNKNNMASAIGIILFIIVAGFSLYNYRRTKSFQEEDMIQ

Crispr_ID: NZ_LN831776_34

• CRISPR_ID: NZ_LN831776_34
• CRISPR_location: 2668181-2668256
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_34

Consensus_repeat	Method
GCAGAAATACCGTTGTAGAAGAGCC	CRISPRCasFinder

spacers of NZ_LN831776_34

>34.1|2668206|26|NZ_LN831776|CRISPRCasFinder
AGCGGCCGGGTTGCCCAGAAACAACA

CRISPR arrays and Neighbor proteins around NZ_LN831776_34

CRISPR arrays

The CRISPR arrays of NZ_LN831776_34

>merge|NZ_LN831776|34|2668181-2668256|CRISPRCasFinder
GCAGAAATACCGTTGTAGAAGAGCCAGCGGCCGGGTTGCCCAGAAACAACAGCAGAAATGCCGTTGTAGAAGAGCC

>NZ_LN831776|34|36|2668181-2668256|CRISPRCasFinder
GCAGAAATACCGTTGTAGAAGAGCC	AGCGGCCGGGTTGCCCAGAAACAACA
GCAGAAATGCCGTTGTAGAAGAGCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_144412097.1|2658996_2665719_-|DUF11-domain-containing-protein	unknown	unknown	gnl|CDD|273634
NZ_LN831776.1|WP_046506732.1|2656051_2657212_-|sporulation-protein-YhbH	unknown	unknown	gnl|CDD|274336
NZ_LN831776.1|WP_020428212.1|2648731_2650045_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_020428220.1|2657323_2659000_-|DUF11-domain-containing-protein	unknown	unknown	gnl|CDD|273634
NZ_LN831776.1|WP_020428227.1|2668919_2669297_+|DUF423-domain-containing-protein	unknown	unknown	gnl|CDD|225238
NZ_LN831776.1|WP_039787967.1|2653242_2654184_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_046502261.1|2666712_2667627_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046506735.1|2665869_2666508_-|hypothetical-protein	unknown	unknown	gnl|CDD|369777
NZ_LN831776.1|WP_020428213.1|2650041_2650890_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226354
NZ_LN831776.1|WP_020426760.1|2674119_2675346_+|cysteine-desulfurase	unknown	unknown	gnl|CDD|131034
NZ_LN831776.1|WP_020426762.1|2672011_2672794_+|Fe-S-cluster-assembly-ATPase-SufC	unknown	unknown	gnl|CDD|223473
NZ_LN831776.1|WP_020426759.1|2675332_2675773_+|SUF-system-NifU-family-Fe-S-cluster-assembly-protein	unknown	unknown	gnl|CDD|273918
NZ_LN831776.1|WP_020428214.1|2650990_2653045_+|methyl-accepting-chemotaxis-protein	unknown	unknown	gnl|CDD|223910
NZ_LN831776.1|WP_020426763.1|2671269_2671731_+|DNA-starvation/stationary-phase-protection-protein	unknown	unknown	gnl|CDD|153102
NZ_LN831776.1|WP_020426758.1|2675792_2677190_+|Fe-S-cluster-assembly-protein-SufB	unknown	unknown	gnl|CDD|131035
NZ_LN831776.1|WP_020428216.1|2654292_2655798_+|alpha-glucosidase/alpha-galactosidase	unknown	unknown	gnl|CDD|185035
NZ_LN831776.1|WP_020428228.1|2669392_2669917_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020428229.1|2670140_2670443_+|DUF1805-domain-containing-protein	unknown	unknown	gnl|CDD|225912
NZ_LN831776.1|WP_020428226.1|2668289_2668748_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426761.1|2672821_2674123_+|Fe-S-cluster-assembly-protein-SufD	unknown	unknown	gnl|CDD|223791

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_144412097.1|2658996_2665719_-|DUF11-domain-containing-protein	gnl|CDD|273634	TIGR01451, unnamed_protein_product, conserved repeat domain. This model represents the conserved region of about 53 amino acids shared between regions, usually repeated, of proteins from a small number of phylogenetically distant prokaryotes. Examples include a 132-residue region found repeated in three of the five longest proteins of Bacillus anthracis, a 131-residue repeat in a cell wall-anchored protein of Enterococcus faecalis, and a 120-residue repeat in Methanobacterium thermoautotrophicum. A similar region is found in some Chlamydial outer membrane proteins.	7.51932e-09
NZ_LN831776.1|WP_046506732.1|2656051_2657212_-|sporulation-protein-YhbH	gnl|CDD|274336	TIGR02877, Stress_response_UPF0229_protein_YhbH, sporulation protein YhbH. This protein family, typified by YhbH in Bacillus subtilis, is found in nearly every endospore-forming bacterium and in no other genome (but note that the trusted cutoff score is set high to exclude a single high-scoring sequence from Nitrosococcus oceani ATCC 19707, which is classified in the Gammaproteobacteria). The gene in Bacillus subtilis was shown to be in the regulon of the sporulation sigma factor, sigma-E, and its mutation was shown to create a sporulation defect. [Cellular processes, Sporulation and germination].	0
NZ_LN831776.1|WP_020428212.1|2648731_2650045_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	3.04194e-68
NZ_LN831776.1|WP_020428220.1|2657323_2659000_-|DUF11-domain-containing-protein	gnl|CDD|273634	TIGR01451, unnamed_protein_product, conserved repeat domain. This model represents the conserved region of about 53 amino acids shared between regions, usually repeated, of proteins from a small number of phylogenetically distant prokaryotes. Examples include a 132-residue region found repeated in three of the five longest proteins of Bacillus anthracis, a 131-residue repeat in a cell wall-anchored protein of Enterococcus faecalis, and a 120-residue repeat in Methanobacterium thermoautotrophicum. A similar region is found in some Chlamydial outer membrane proteins.	1.44429e-08
NZ_LN831776.1|WP_039787967.1|2653242_2654184_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	4.52473e-28
NZ_LN831776.1|WP_020428213.1|2650041_2650890_+|sugar-ABC-transporter-permease	gnl|CDD|226354	COG3833, MalG, ABC-type maltose transport systems, permease component [Carbohydrate transport and metabolism].	3.22067e-106
NZ_LN831776.1|WP_046506735.1|2665869_2666508_-|hypothetical-protein	gnl|CDD|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	2.08425e-09
NZ_LN831776.1|WP_020428227.1|2668919_2669297_+|DUF423-domain-containing-protein	gnl|CDD|225238	COG2363, COG2363, Uncharacterized small membrane protein [Function unknown].	2.36573e-33
NZ_LN831776.1|WP_020426760.1|2674119_2675346_+|cysteine-desulfurase	gnl|CDD|131034	TIGR01979, Probable_cysteine_desulfurase, cysteine desulfurases, SufSfamily. This model represents a subfamily of NifS-related cysteine desulfurases involved in FeS cluster formation needed for nitrogen fixation among other vital functions. Many cysteine desulfurases are also active as selenocysteine lyase and/or cysteine sulfinate desulfinase. This subfamily is associated with the six-gene SUF system described in E. coli and Erwinia as an FeS cluster formation system during oxidative stress. The active site Cys is this subfamily resembles GHHC with one or both His conserved. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	0
NZ_LN831776.1|WP_020426762.1|2672011_2672794_+|Fe-S-cluster-assembly-ATPase-SufC	gnl|CDD|223473	COG0396, sufC, Cysteine desulfurase activator ATPase [Posttranslational modification, protein turnover, chaperones].	1.33464e-143
NZ_LN831776.1|WP_020426759.1|2675332_2675773_+|SUF-system-NifU-family-Fe-S-cluster-assembly-protein	gnl|CDD|273918	TIGR01994, Iron-sulfur_cluster_assembly_scaffold_protein_IscU, SUF system FeS assembly protein, NifU family. Three iron-sulfur cluster assembly systems are known so far. ISC is broadly distributed while NIF tends to be associated with nitrogenase in nitrogen-fixing bacteria. The most recently described is SUF, believed to be important to maintain the function during aerobic stress of enzymes with labile Fe-S clusters. It is fairly widely distributed. This family represents one of two different proteins proposed to act as a scaffold on which the Fe-S cluster is built and from which it is transferred. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	3.75353e-67
NZ_LN831776.1|WP_020428214.1|2650990_2653045_+|methyl-accepting-chemotaxis-protein	gnl|CDD|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	1.67324e-41
NZ_LN831776.1|WP_020426763.1|2671269_2671731_+|DNA-starvation/stationary-phase-protection-protein	gnl|CDD|153102	cd01043, DPS, DPS protein, ferritin-like diiron-binding domain. DPS (DNA Protecting protein under Starved conditions) domain is a member of a broad superfamily of ferritin-like diiron-carboxylate proteins. Some DPS proteins nonspecifically bind DNA, protecting it from cleavage caused by reactive oxygen species such as the hydroxyl radicals produced during oxidation of Fe(II) by hydrogen peroxide. These proteins assemble into dodecameric structures, some form DPS-DNA co-crystalline complexes, and possess iron and H2O2 detoxification capabilities. Expression of DPS is induced by oxidative or nutritional stress, including metal ion starvation. Members of the DPS family are homopolymers formed by 12 four-helix bundle subunits that assemble with 23 symmetry into a hollow shell. The DPS ferroxidase site is unusual in that it is not located in a four-helix bundle as in ferritin, but is shared by 2-fold symmetry-related subunits providing the iron ligands. Many DPS sequences (e.g., E. coli) display an N-terminal extension of variable length that contains two or three positively charged lysine residues that extends into the solvent and is thought to play an important role in the stabilization of the complex with DNA. DPS Listeria Flp, Bacillus anthracis Dlp-1 and Dlp-2, and Helicobacter pylori HP-NAP which lack the N-terminal extension, do not bind DNA. DPS proteins from Helicobacter pylori, Treponema pallidum, and Borrelia burgdorferi are highly immunogenic.	4.37088e-57
NZ_LN831776.1|WP_020428216.1|2654292_2655798_+|alpha-glucosidase/alpha-galactosidase	gnl|CDD|185035	PRK15076, PRK15076, alpha-galactosidase; Provisional.	0
NZ_LN831776.1|WP_020426758.1|2675792_2677190_+|Fe-S-cluster-assembly-protein-SufB	gnl|CDD|131035	TIGR01980, UPF0051_protein_slr0074, FeS assembly protein SufB. This protein, SufB, forms a cytosolic complex SufBCD. This complex enhances the cysteine desulfurase of SufSE. The system, together with SufA, is believed to act in iron-sulfur cluster formation during oxidative stress. Note that SufC belongs to the family of ABC transporter ATP binding proteins, so this protein, encoded by an adjacent gene, has often been annotated as a transporter component. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	0
NZ_LN831776.1|WP_020428229.1|2670140_2670443_+|DUF1805-domain-containing-protein	gnl|CDD|225912	COG3377, COG3377, Uncharacterized conserved protein [Function unknown].	1.1922e-29
NZ_LN831776.1|WP_020426761.1|2672821_2674123_+|Fe-S-cluster-assembly-protein-SufD	gnl|CDD|223791	COG0719, SufB, Cysteine desulfurase activator SufB [Posttranslational modification, protein turnover, chaperones].	1.32713e-125

Protein sequences

>NZ_LN831776.1|WP_046502261.1|2666712_2667627_+|hypothetical-protein
MKSQRKLPVLAAIAVLMLAITACGGNTPAEAPGEPSPTASPSPAESAASPSPSPAAQPSSSPAEESQVIQGTGIYVGQIDNHSVEIKTEEGATSFELGTGLEEAPEALSMDDPVVFEYVERSVEGDSSVLQRVLSKLEKSADSGSAAPSQAALPKSKSFSLTLEGMKEEKTAALAAGNGYSLYVFDIFTFDAKTGRLAMKVDPEYYAEITKLPSDFDLDSLKQEGEKELSSTGKVTALDQKERDRRMSGIRLYLTAMGNGLTREYAVKEIAGQGYVIRLNIPQREASEGFGPHVYTSLDSLVSQ
>NZ_LN831776.1|WP_046506735.1|2665869_2666508_-|hypothetical-protein
MKIDIGCGSGKETGYLGIDRTAWPGVDIICDINEGIPLPDNTAEFVMASRVLPYVNNLFAVMAEIYRISIHKAVICILAPYAHSFPHLSNPLFKQKFDEYTPRYFTGSFFQPAAGAVSPEIPDYPAPVPPFDYRLLRMELFYQYPFDDTLYEAEELEILKTLQSNVVHEIMYHFVVVKKPVTLEELADMSRKTYPEPQALLKRRRHTQNRQV
>NZ_LN831776.1|WP_144412097.1|2658996_2665719_-|DUF11-domain-containing-protein
MKIIPLVVRATINATGAITFTGNTLGLSRSDTTGVPGTQDSIGAFATVNTASVFGTYPAGTTSLYQNNSSSAILTIPSGSTVLYAELIWGGSYINGSVNLSSAINNPVSFTTPAGTTSSVSPDSATSNSVDLGNGALAYVRSANVTSIIQAGGAGTYTTGGVVGTIVITGDSTANHAGWTLGVIYQNPSLPFRNMSLRAGAVLVQASSAPVATTITGFATPVSGALGGRILFSAQEGDANRSGDQALFGPTSNTQVALSGPNNFANNFFASQINNDTGALNTTGTFGTRNQTNGSPGTNIIGGRQGWDITNVDVSARLVNNQSSALLTLTTSGDAYVVNGNALQIDINAPKISLTKGSNVAGTVVGDTVTYTVTVSNTGTASATSAVLSDTLPAGLTFVNRSVVVAGVYRPSYDITAGVPLGTLTLGTSATVTYQATVTSLPAPQTVANTANVAFTFQSVAGGPIVTGVIPSNTDTLPVYSPVLGIVKSASTANATVGDQITYTLQITNTGNIGAATVITDNIPAGSSYVPGSFTVNGTPTAGNPSTGISIGTVPAGGSTTVQFQVQVNSLPSPPQLVDQATAAYTFLVPDGRTLAGTAASNTLTIPVALPNVAVVKSAGFTDAAVGDILLYTSVISNNGIAPVTNVVLSDPVPAGSSFVPESVSVAGAARPSADPATGITVGTVAAGTSVTVTFQVNVTSVPSPAQLSNRSSASYSSGVFTGISQSNTTVTPVYQPVITIVKSASTASATVGGNVLYTLRVQNTGNLAAAVVLSDNIPAGSAFVAGSVTVNGVARPSDSPTGGIALGAVAAGAAVTVTFLTAVQSLPSPPVLNNQGSSSYTYQLPSGRSLSGASLSNTVSLPVSAPGITLLKNASLASMAVGENLTYTVAVSNPSGVSVNNVILSDPVPAGASFVAGSVTVNGASLPSANPGAGISLGTIAAGATSTVAFQVNAALLPNPAVFTNKASASFTAGAFSGTALSNTVSTSVYIPVINLVKSANAAQASVGSSLSFTILVSNTGNIAAVLNLTDALPPQAVFETNSVSIGGTPLPGYSPAAGIPVGPLAPGDSVPVSFLVTVTALPPNQQLLNSAAASFTFTLPDGRQLGGNAASNTLAVPVSAPNVSIVKSVNAIDAVTGDILTFTSVLTNNSIAAVSHIILSDPLPENAAFIPGTVIVGGVSQPLSVPSAGIPIGSLGPEASVAVTFEVRITMPIPSQINNQSTVSFTSGVFSGSSSSNITSTPVIQPQISLVKSANALNATVGDTVIYTVAVSNAGNLAANVTLTDNIPAGTVFDPNSVIVGGFPQPGTAPDTGITVGTVAPGASIPVSFTVIIVSLPSPQQLVNQAASTFTYTPPDGRLLTGTAVSNTVTVAVSAPNVAVVKSTTATAAALGDTIPFSVNITNTDAEPVNSVQLSDPTPPGTTFVTGSVSVNGVPFTNANPATGVSVGTIAPGASANVTYNVTVTSAPASAAINNQATVTYTSGVAFSGSTISNTVSVPFYQPVLSAVKSASTANATVGDTVTYTLTVSNTGNYPAALTVKDTIPAGTAFQPNSVLINGLPLPQADPAAGIAAGTIAAGATVAVVFSVVITSLPSPQLLVNQGTAAYSFTLPDGRTLNGSVLSNTVTIPVTNPNLAVVKTTATTATTLGDTIVYSVTLTNNGIAAVNNVVFTDALPSGTAFVPGSVLVNGVARPAASPSTGITIGSIAPGASVTVAFSVTVNSLPGSGLLNNQSSVSFTSGALSSVAFSNIVTTPVYQPVIGAAKSASTVKATVGDTIIYTVNVSNTGNYPATATLTDTIPAGSTLVPNSVLINGFPSPGANPATGIALGTIAAGTTLAVTFSVVIDTLPVSQQLSNQATVSFAFTLPDGRTFNQAAVSNINQISVSAPNVQVVKSSPATDAVIGDTVTYSITVTNNGIEAITNAVLSDPVPAGASFASSSVVVDGTPLPGANPANGIALGTIAPGASSLVTFSILVNALPASGTLSNQASVSFTSGAFSGASYSNTFVTPVYQPFINIVKGADTANATVGDTVTYSLKVTNTGNLAANVTITDSIPAGAVFIPNSVLVNGVPQPGADPASGLNIGTVAPGATITVTITLQVTVASLPSPQQLVNQAAATFTFSPPDGRLLSGSSESNVLVIPVSSPDVTAVKSTPAVDAVVGDIITYTIAVTNNGIESVNNVVLVDPIPAGSQFVAGSVTVDGVPRTGANPAAGIVIGTITPGDSVTVTFQVQVIAV
>NZ_LN831776.1|WP_020428220.1|2657323_2659000_-|DUF11-domain-containing-protein
MIRDSRLQPVVSNQSMVLYSSAAGADVITYSNTVNTPVVGPVLTLVKSADHTSASLGETLVYTLIARNEGNAPALTTLVDALPSGVSFVANSVLRDGVPLPGVSPFSGILLGAVAPQTEVRIAFQVIVVSLPPSLELGNRARAVYSFTTPEGRHVEGEVFSNQITVSLLAYKLSILLASSTPTTFVGDAVTFTLRVRNEGTRLMSGILTTLPVPEGAIFLPGSVISGGIYSPDADPDKGIPLPPLDPGKTADISFQVRVVSVPALTAQAVVTYDADGDTDGTKSNTVTVAVIQSGLSVSLKVDKYSAAPGDRLGYRFTIRNSGKLAVDAMLAGAIPSGTLFVWDSVHIDGIPQRGVHPGEGIPLGTIRAGSAAVVDLLVSIPAEADILQMPAIQNQGSVEYTFTLPDGRNVRERVRSNTVTTLLFSPVISIEMTGEPPMVEPGGIAEFNIAVTNSGNYPAEVSVIQIIPQGCTLETGKVTISVHTVPESKYSGIVSLGVMDPGQTAQLSYLVRVHPGYMGSALQGSSTALYLYTIDGRRYSGEARSNSYKLMIEEISE
>NZ_LN831776.1|WP_046506732.1|2656051_2657212_-|sporulation-protein-YhbH
MPQSSGHSAFVVSKEDWSLHRKGHQDQERHQQKVREAIKDNLPDLVTEENIIMSDGKQIVKVPIRSLDEYRIIYNFRKQKHVGQGDGESQVGDVLGRDSQSAHPGKGDKAGDQPGQDTVEAEVDLEDLEDILFEDMELPHLAPKTQEEIEVKSIVFNDIRKKGMMSNIDKKRTLLENLRRNASRGKPGIHSISPDDLRYKTWDDITVPHSNAVIIAMMDTSGSMGTFEKYCARSFFFWMTRFLRRQYEKVEIVFLAHHTEAKEVSEHDFFTRGESGGTICSSAYQKALDIIDSRYPPAKYNIYPFHFSDGDNLTSDNERCVKLIGELLKRSNMFGYGEVNQYNRSSTLMSAYRHLKQEQFMHYVIKDKKEVYQALKTFFGKREAVK
>NZ_LN831776.1|WP_020428216.1|2654292_2655798_+|alpha-glucosidase/alpha-galactosidase
MSFKVAFIGAGSIGFTRGLLRDLLTVAEFKEIEVSFMDINPHNLQMVNELCQRDIRENGLKIVISATTDRKEALKDAKYVFCTIRMGGLEAFATDVDIPLKYGVDQCVGDTLCAGGIMYGQRGIAEMLEICRDIREAAAPDVLLLNYSNPMAMLTWACNKYGGVRTIGLCHGVQHGHQQIAEVYGLEKSEVDIICAGINHQTWYISAKHKGRDLTGGLLEAFEKHPEFSRTEKVRIDMLRRFGYYSTESNGHLSEYVPWYRKRSGEIMDWIDLGSWINGETGGYLRVCTEGRNWFETDFPNWMKDPALEYTSEHRGEEHGSYIIEGLETGRVYRGHFNTVNNGIITNLPDDAVIEAPGYVDHNGISMPVVGDLPLGPAAVCNVSISVQRLAVEAAVHGDDKLLRQAFMMDPLVGAVCNPKEIWQMVDEMLVAGEAWLPQYSAAIAEAKVRLASGDLVPTLADNAGAARLKVKSVDEMMQDREAANKNAGESDKGKDREKVR
>NZ_LN831776.1|WP_039787967.1|2653242_2654184_+|helix-turn-helix-transcriptional-regulator
MNGSLFQQALLDGEYGPHFFAYYYKQWNPYTMAFHQHNSTEIMYLISGSCVVEVRQEPDEEERFRLKRGELIMLDANVPHRLIVEEGTSCRMLNVEFGFTAASGAVPSIARLAEAEADLAGLLREPFRSLVLPDPEEVFHVLKSLVLELDQHGVEGEGQGKGRGSIMTGLLFSELLLRLSRLRREQLQASQQPAQLYVRRAVEFLHQNYDRSIQVKEVAAEVSLHPGYLHRIFRAHTGRTLTGYLNMLRIEKARMLLGQSEIPVAEIADYVGISSRQYFHLLFKKYTRCTPVEYRNSLERFSWSDAQPDIQDR
>NZ_LN831776.1|WP_020428214.1|2650990_2653045_+|methyl-accepting-chemotaxis-protein
MKQPRNSRFRSVGMKLFVILFCTIVLLSSVLGLTSYYAAKGIITDQVAAASSQSIVQAADKLDFLFAEYEALSRQFAVDSILKADMETVSRPGAATVAKVEAEDRIRRKLDSVKGSDERLLGIRLVSKSLVDAESYKSTGISSVRSAEGIQARVKQLDAAKGNPVWFPVRAKGFFDMYDQSSLTMGRLLRNMQHPEAEYYMLIEIKGQALTDILSNLHIGLTGEIRILDPDGNIVYGADNKLLGEPSYIHPAAEPAEGQQQSFTASNEQGTSQLVVYQPLDTAKWTLMGYAPVSDFTKSADRLLYITLSVVLAAAVIALVIGYVLVRLIGRPLGKLAGLMEEGEQGNLQVRTHFKGQDEIGRLGHSFNKMMEQISLLAGQSNRSAAQVLATSEQLVNASSITSTHAREVAAATGEIAHGAASLALEAESSNRNVERMNLQITEVKEINSAMDASAEKVITVSDQGAELMKTLVAQSESTVQMMELIQENSMKLRESAHLIRSILTPMIAVNKQTNILALNASIEAVRAGAAGRGFAVIANEIRGLADESNQSIAMVSKITEEISSRIENTVQVVGDTAPLFREQISSVRESSSIFEGVRAEMEQFIGYLNESSASITELMEYQHQLGESMASVHAVVQQTSASTEEVASMSSQQFTVSEELVALSGKLEKLAEELKQSLVSFHG
>NZ_LN831776.1|WP_020428213.1|2650041_2650890_+|sugar-ABC-transporter-permease
MIIGRKLANFFRLGFSYIILIALAVAAIYPALWILLSSFRPGKSLYSKTLIPEHFTLDHYKELFTSPVYMFGTWYANTLKIAVFSMLIGVVLTLLTSYALSRFRFKTRKTTMSVLLILGMFPGFMSMIAIYLLLKEFNLLDTHLALIIVYAAGAPLGGTLIAKGFLDTVPRSLDEAARIDGASNFGIFARIILPLSRPMITYMALTQFVGPWVDFIFAKLILRTKDNWTVAVGMWDMVNTMQNSNFTLFAAGAVLISVPIMILFAFLQRLLVDGLTAGASKG
>NZ_LN831776.1|WP_020428212.1|2648731_2650045_+|sugar-ABC-transporter-permease
MQRHRTRAAILSTIFMGLGQIYNRQFIKGLIFIAVEAGALVYFIANLGEAFWGITTLGDSPSHLEKVKGIAKMVPGDHSIVILIQSLITLMFFVLFLIAWYMNIRDAHKTGEERETGRPSNTFKQSVRYILDYKFAQSFLLLPGIGILFFTIMPIIFMIMLAFTNYAAPDHIPPAKLVDWVGFETFRNLLVLKSWSHTFYGVLTWTIIWAVLSTITTYFGGMLVALLINQKGIRFKGLWRLILIVPYAIPQMISLLLMRNLFNGQFGPINQYLGYFGLGGLPWLTDPFWAKVTVIMVNMWVGIPVSMLLIMGVLTTIPRDMYEAAEVDGATNYQKFRIVTLPMILFSTAPTLIMQFAGNINNFNAIYLLTQGNPVNGNYQYAGSTDLLVTWLYKLTLDQNKNNMASAIGIILFIIVAGFSLYNYRRTKSFQEEDMIQ
>NZ_LN831776.1|WP_020428226.1|2668289_2668748_-|hypothetical-protein
MDDYSTPHTDPSSPRPQSTVPETGLPPQQHAMYEENKRDFKHSGPGIASFIIALITLIGYIIAFVVVGVRSSSLVNGSDSFIADSAEAIFYLGISVLILAAFNVIGGVLGIIGLTLRKRRKVFGIIGTIINAVFLLLFMLIISTVLVNAGSV
>NZ_LN831776.1|WP_020428227.1|2668919_2669297_+|DUF423-domain-containing-protein
MQRRFMAWGALLAMLSVGIGAFGAHLLKPVISEDYLKVYETGVHYHMIHALGLILIGLAAGQWGERSRLRWAGRLLILGIILFSGSLYALSITGIKVLGAITPLGGVCFLAGWLCLAWEALSRNK
>NZ_LN831776.1|WP_020428228.1|2669392_2669917_-|hypothetical-protein
MDKKLQHTDGNYLFNVDILINARTNPLALQYLLEILNSNDKITDFNINSGLELGRTIDHLLRSAKLALKHESAAAVQVPVKLPVKPTDKQAGKPVSGSIPADAPGETPADAYGKIRLYIQNNQLVRLRANRHGKQVSMPCRILNFDEAANSISVYHVDEKQVYTFKLNEIDEFS
>NZ_LN831776.1|WP_020428229.1|2670140_2670443_+|DUF1805-domain-containing-protein
MVTMEPVNVGGHILVGVEVKLPKTTLLSISTGKGYIMCGALDVGLLNETLSDRGIIAARAVGVRTLPQLLAAPLESVTIEAEKLGIVPGMTGADALLHML
>NZ_LN831776.1|WP_020426763.1|2671269_2671731_+|DNA-starvation/stationary-phase-protection-protein
MAKASNKVTTTSLEQVLNREVANLNVLYVKIHNYHWYVKGEQFFSLHVKFEELYDDVTLKMDEVAERLLSIKGSPAATMKEYLELATIQEATGKEDTRGMVQTLIEDFATVAEELTEGIELAEQVSDQPTADLFIKIRSDLEKNQWMLRSFLG
>NZ_LN831776.1|WP_020426762.1|2672011_2672794_+|Fe-S-cluster-assembly-ATPase-SufC
MAADFVIEGLKATIEGKEILKGINLQMKGGEIHAIMGPNGTGKSTLASALMGHPKYEVTEGTAVLEGEDLLEMAVDERARAGLFLAMQYPSEISGVTNSDFLRSAINSRREEGNEISLIRFIRQMEAKMKELDMNPEFLHRYLNEGFSGGEKKRNEILQMMMLDPKIVILDEIDSGLDIDALKIVAEGVNSMRSPERGFLVITHYQRLLNYIKPDFVHVMMQGRIVKSGGPELAERLEAEGYEWVKEELGIEDETVGQEA
>NZ_LN831776.1|WP_020426761.1|2672821_2674123_+|Fe-S-cluster-assembly-protein-SufD
MTTQTILPVDAQLLTDWSQSSGEPGWLKDSRLNALTLAAGLALPKLEKTRIDRWNVNNYGTYKAGQTITALSEAPASVAALIKDQEEGSLIIQRNSGAIYVRLAPELAAQGVIFTDLQTAVKEHGDLVQRYLHKAVLPDEHSLAALHAALWNGGVFLYVPKNVVVETPLQAVLLTDDAEAAFVPHILIVADTNSSVTYVDNYVSDKTEAGLHNGAVEVFVGAGAKVRYATVHQLGEDTTDVTYRRAVVENDGTIEWIVGEMNYGDTASDTKSVLKGNGASSDAKVIAVGSGSQKLNYTTQAQHFGKNTPSDMITRAVMRDAATSIINGITKIEKGATRADGQQTEKVLMLSPQARGDANPILLIDEDDVTAGHAASVGQVNYEQVYYLMSRGISRHDAETLIIYGFLAPVVSQIPLEGLRNQLQSLVERKLGQ
>NZ_LN831776.1|WP_020426760.1|2674119_2675346_+|cysteine-desulfurase
MISSAIREQFPILNQTINGHPLVYLDSAATSQKPRQVIEAVKSYYEWDNSNVHRGVHTLGSRATDAYEGAREKLAKFINARSTKEIIFTRGTTTALNIVASSYGPGNVGEGDEIVITQMEHHSNFIPWQQLAKKTGATLKFIPLQKDGSITLEDAEQTITDKTKIVAIAYVSNVMGISHPVKELAAIAHRHGAVIVVDGAQSTPHMKVDVQDLDCDFYALSGHKMLAPTGIGALYGKKALLEAMEPVEFGGEMIDDVGLYDSTWKELPWKFEGGTPIIAGAVGLGAAIDFLQEIGLDEIHRHEMELAAYAEQRLSEVDGLTIYGPRNRKVGVVTFNLGDVHPHDVATVLDAEGVAVRAGHHCCQPLMRWLQVSSTARASFYLYNSEQDVDALVQALIKAKEYFGYELG
>NZ_LN831776.1|WP_020426759.1|2675332_2675773_+|SUF-system-NifU-family-Fe-S-cluster-assembly-protein
MNLDDLYRRVIMDHYKNPRNRGSFADDALKIELNNPTCGDRITLQLKVEDGVVKDARYSGEGCSISMSSASMMTEAVKGQTVEHALELADRFSSLMKGEAVDFEDYEDIEALSGVNKFPARIKCATLAWNALRKGIDVEEEHHQEH
>NZ_LN831776.1|WP_020426758.1|2675792_2677190_+|Fe-S-cluster-assembly-protein-SufB
MAKKAPDMEEYQYGFRDEHKSIFQSGKGLTAEIVKEISAIKNEPEWMLDFRLKALEQFYKMPMPKWGGNLDELDFDDIQYYVRPSEKQGKTWEEVPSEIKETFDKLGIPEAEQKFLAGVSAQYESEVVYHSMQKNLEDQGVIFTDTDTALREHPELFKKFFGTIIPPADNKFAALNSAVWSGGSFIYVPKGVKCEVPLQAYFRINSENMGQFERTLILADEDSFVHYVEGCTAPIYSTNSLHSAVVEILCMKNARVRYTTIQNWAPNIYNLVTKRAVAEENATMEWVDGNIGSKLTMKYPAVVLKGRGAKGSVLSIAVAGKDQHQDAGAKMIHLAPDTTSTIVSKSISKHGGKVTYRGLASFGRKAEGAKSNIKCDTLILDNQSTSDTIPYNEIMNDNIVLEHEATVSKVSEEQLFYLMSRGLTEAEATQMIVMGFIEPFTKELPMEYAVEMNRLIKFEMEGSIG

Crispr_ID: NZ_LN831776_35

• CRISPR_ID: NZ_LN831776_35
• CRISPR_location: 2670857-2670931
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_35

Consensus_repeat	Method
AATTAGTGTCCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_35

>35.1|2670880|29|NZ_LN831776|CRISPRCasFinder
CATCTACCCGAGGGTAGGGTACTCCGGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_35

CRISPR arrays

The CRISPR arrays of NZ_LN831776_35

>merge|NZ_LN831776|35|2670857-2670931|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTTCATCTACCCGAGGGTAGGGTACTCCGGCAAATTAGTGTCCCTTTTTCCACTT

>NZ_LN831776|35|37|2670857-2670931|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTT	CATCTACCCGAGGGTAGGGTACTCCGGCA
AATTAGTGTCCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_144412097.1|2658996_2665719_-|DUF11-domain-containing-protein	unknown	unknown	gnl|CDD|273634
NZ_LN831776.1|WP_046506732.1|2656051_2657212_-|sporulation-protein-YhbH	unknown	unknown	gnl|CDD|274336
NZ_LN831776.1|WP_020426760.1|2674119_2675346_+|cysteine-desulfurase	unknown	unknown	gnl|CDD|131034
NZ_LN831776.1|WP_020428220.1|2657323_2659000_-|DUF11-domain-containing-protein	unknown	unknown	gnl|CDD|273634
NZ_LN831776.1|WP_046502276.1|2679283_2680750_+|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_LN831776.1|WP_081487111.1|2678518_2678629_+|divergent-PAP2-family-protein	unknown	unknown	gnl|CDD|376897
NZ_LN831776.1|WP_046502261.1|2666712_2667627_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046506735.1|2665869_2666508_-|hypothetical-protein	unknown	unknown	gnl|CDD|369777
NZ_LN831776.1|WP_020428227.1|2668919_2669297_+|DUF423-domain-containing-protein	unknown	unknown	gnl|CDD|225238
NZ_LN831776.1|WP_020426762.1|2672011_2672794_+|Fe-S-cluster-assembly-ATPase-SufC	unknown	unknown	gnl|CDD|223473
NZ_LN831776.1|WP_020426759.1|2675332_2675773_+|SUF-system-NifU-family-Fe-S-cluster-assembly-protein	unknown	unknown	gnl|CDD|273918
NZ_LN831776.1|WP_020426758.1|2675792_2677190_+|Fe-S-cluster-assembly-protein-SufB	unknown	unknown	gnl|CDD|131035
NZ_LN831776.1|WP_167345606.1|2677670_2677931_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426763.1|2671269_2671731_+|DNA-starvation/stationary-phase-protection-protein	unknown	unknown	gnl|CDD|153102
NZ_LN831776.1|WP_020426753.1|2680746_2681436_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_LN831776.1|WP_020428216.1|2654292_2655798_+|alpha-glucosidase/alpha-galactosidase	unknown	unknown	gnl|CDD|185035
NZ_LN831776.1|WP_020428228.1|2669392_2669917_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020428229.1|2670140_2670443_+|DUF1805-domain-containing-protein	unknown	unknown	gnl|CDD|225912
NZ_LN831776.1|WP_020428226.1|2668289_2668748_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426761.1|2672821_2674123_+|Fe-S-cluster-assembly-protein-SufD	unknown	unknown	gnl|CDD|223791

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_144412097.1|2658996_2665719_-|DUF11-domain-containing-protein	gnl|CDD|273634	TIGR01451, unnamed_protein_product, conserved repeat domain. This model represents the conserved region of about 53 amino acids shared between regions, usually repeated, of proteins from a small number of phylogenetically distant prokaryotes. Examples include a 132-residue region found repeated in three of the five longest proteins of Bacillus anthracis, a 131-residue repeat in a cell wall-anchored protein of Enterococcus faecalis, and a 120-residue repeat in Methanobacterium thermoautotrophicum. A similar region is found in some Chlamydial outer membrane proteins.	7.51932e-09
NZ_LN831776.1|WP_046506732.1|2656051_2657212_-|sporulation-protein-YhbH	gnl|CDD|274336	TIGR02877, Stress_response_UPF0229_protein_YhbH, sporulation protein YhbH. This protein family, typified by YhbH in Bacillus subtilis, is found in nearly every endospore-forming bacterium and in no other genome (but note that the trusted cutoff score is set high to exclude a single high-scoring sequence from Nitrosococcus oceani ATCC 19707, which is classified in the Gammaproteobacteria). The gene in Bacillus subtilis was shown to be in the regulon of the sporulation sigma factor, sigma-E, and its mutation was shown to create a sporulation defect. [Cellular processes, Sporulation and germination].	0
NZ_LN831776.1|WP_020428220.1|2657323_2659000_-|DUF11-domain-containing-protein	gnl|CDD|273634	TIGR01451, unnamed_protein_product, conserved repeat domain. This model represents the conserved region of about 53 amino acids shared between regions, usually repeated, of proteins from a small number of phylogenetically distant prokaryotes. Examples include a 132-residue region found repeated in three of the five longest proteins of Bacillus anthracis, a 131-residue repeat in a cell wall-anchored protein of Enterococcus faecalis, and a 120-residue repeat in Methanobacterium thermoautotrophicum. A similar region is found in some Chlamydial outer membrane proteins.	1.44429e-08
NZ_LN831776.1|WP_081487111.1|2678518_2678629_+|divergent-PAP2-family-protein	gnl|CDD|376897	pfam02681, DUF212, Divergent PAP2 family. This family is related to the pfam01569 family (personal obs: C Yeats).	4.73952e-10
NZ_LN831776.1|WP_046506735.1|2665869_2666508_-|hypothetical-protein	gnl|CDD|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	2.08425e-09
NZ_LN831776.1|WP_020428229.1|2670140_2670443_+|DUF1805-domain-containing-protein	gnl|CDD|225912	COG3377, COG3377, Uncharacterized conserved protein [Function unknown].	1.1922e-29
NZ_LN831776.1|WP_020428227.1|2668919_2669297_+|DUF423-domain-containing-protein	gnl|CDD|225238	COG2363, COG2363, Uncharacterized small membrane protein [Function unknown].	2.36573e-33
NZ_LN831776.1|WP_020426762.1|2672011_2672794_+|Fe-S-cluster-assembly-ATPase-SufC	gnl|CDD|223473	COG0396, sufC, Cysteine desulfurase activator ATPase [Posttranslational modification, protein turnover, chaperones].	1.33464e-143
NZ_LN831776.1|WP_020426759.1|2675332_2675773_+|SUF-system-NifU-family-Fe-S-cluster-assembly-protein	gnl|CDD|273918	TIGR01994, Iron-sulfur_cluster_assembly_scaffold_protein_IscU, SUF system FeS assembly protein, NifU family. Three iron-sulfur cluster assembly systems are known so far. ISC is broadly distributed while NIF tends to be associated with nitrogenase in nitrogen-fixing bacteria. The most recently described is SUF, believed to be important to maintain the function during aerobic stress of enzymes with labile Fe-S clusters. It is fairly widely distributed. This family represents one of two different proteins proposed to act as a scaffold on which the Fe-S cluster is built and from which it is transferred. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	3.75353e-67
NZ_LN831776.1|WP_046502276.1|2679283_2680750_+|HAMP-domain-containing-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	4.95437e-55
NZ_LN831776.1|WP_020426763.1|2671269_2671731_+|DNA-starvation/stationary-phase-protection-protein	gnl|CDD|153102	cd01043, DPS, DPS protein, ferritin-like diiron-binding domain. DPS (DNA Protecting protein under Starved conditions) domain is a member of a broad superfamily of ferritin-like diiron-carboxylate proteins. Some DPS proteins nonspecifically bind DNA, protecting it from cleavage caused by reactive oxygen species such as the hydroxyl radicals produced during oxidation of Fe(II) by hydrogen peroxide. These proteins assemble into dodecameric structures, some form DPS-DNA co-crystalline complexes, and possess iron and H2O2 detoxification capabilities. Expression of DPS is induced by oxidative or nutritional stress, including metal ion starvation. Members of the DPS family are homopolymers formed by 12 four-helix bundle subunits that assemble with 23 symmetry into a hollow shell. The DPS ferroxidase site is unusual in that it is not located in a four-helix bundle as in ferritin, but is shared by 2-fold symmetry-related subunits providing the iron ligands. Many DPS sequences (e.g., E. coli) display an N-terminal extension of variable length that contains two or three positively charged lysine residues that extends into the solvent and is thought to play an important role in the stabilization of the complex with DNA. DPS Listeria Flp, Bacillus anthracis Dlp-1 and Dlp-2, and Helicobacter pylori HP-NAP which lack the N-terminal extension, do not bind DNA. DPS proteins from Helicobacter pylori, Treponema pallidum, and Borrelia burgdorferi are highly immunogenic.	4.37088e-57
NZ_LN831776.1|WP_020426753.1|2680746_2681436_+|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	4.77846e-87
NZ_LN831776.1|WP_020428216.1|2654292_2655798_+|alpha-glucosidase/alpha-galactosidase	gnl|CDD|185035	PRK15076, PRK15076, alpha-galactosidase; Provisional.	0
NZ_LN831776.1|WP_020426758.1|2675792_2677190_+|Fe-S-cluster-assembly-protein-SufB	gnl|CDD|131035	TIGR01980, UPF0051_protein_slr0074, FeS assembly protein SufB. This protein, SufB, forms a cytosolic complex SufBCD. This complex enhances the cysteine desulfurase of SufSE. The system, together with SufA, is believed to act in iron-sulfur cluster formation during oxidative stress. Note that SufC belongs to the family of ABC transporter ATP binding proteins, so this protein, encoded by an adjacent gene, has often been annotated as a transporter component. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	0
NZ_LN831776.1|WP_020426760.1|2674119_2675346_+|cysteine-desulfurase	gnl|CDD|131034	TIGR01979, Probable_cysteine_desulfurase, cysteine desulfurases, SufSfamily. This model represents a subfamily of NifS-related cysteine desulfurases involved in FeS cluster formation needed for nitrogen fixation among other vital functions. Many cysteine desulfurases are also active as selenocysteine lyase and/or cysteine sulfinate desulfinase. This subfamily is associated with the six-gene SUF system described in E. coli and Erwinia as an FeS cluster formation system during oxidative stress. The active site Cys is this subfamily resembles GHHC with one or both His conserved. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	0
NZ_LN831776.1|WP_020426761.1|2672821_2674123_+|Fe-S-cluster-assembly-protein-SufD	gnl|CDD|223791	COG0719, SufB, Cysteine desulfurase activator SufB [Posttranslational modification, protein turnover, chaperones].	1.32713e-125

Protein sequences

>NZ_LN831776.1|WP_020428229.1|2670140_2670443_+|DUF1805-domain-containing-protein
MVTMEPVNVGGHILVGVEVKLPKTTLLSISTGKGYIMCGALDVGLLNETLSDRGIIAARAVGVRTLPQLLAAPLESVTIEAEKLGIVPGMTGADALLHML
>NZ_LN831776.1|WP_020428228.1|2669392_2669917_-|hypothetical-protein
MDKKLQHTDGNYLFNVDILINARTNPLALQYLLEILNSNDKITDFNINSGLELGRTIDHLLRSAKLALKHESAAAVQVPVKLPVKPTDKQAGKPVSGSIPADAPGETPADAYGKIRLYIQNNQLVRLRANRHGKQVSMPCRILNFDEAANSISVYHVDEKQVYTFKLNEIDEFS
>NZ_LN831776.1|WP_020428227.1|2668919_2669297_+|DUF423-domain-containing-protein
MQRRFMAWGALLAMLSVGIGAFGAHLLKPVISEDYLKVYETGVHYHMIHALGLILIGLAAGQWGERSRLRWAGRLLILGIILFSGSLYALSITGIKVLGAITPLGGVCFLAGWLCLAWEALSRNK
>NZ_LN831776.1|WP_020428226.1|2668289_2668748_-|hypothetical-protein
MDDYSTPHTDPSSPRPQSTVPETGLPPQQHAMYEENKRDFKHSGPGIASFIIALITLIGYIIAFVVVGVRSSSLVNGSDSFIADSAEAIFYLGISVLILAAFNVIGGVLGIIGLTLRKRRKVFGIIGTIINAVFLLLFMLIISTVLVNAGSV
>NZ_LN831776.1|WP_046502261.1|2666712_2667627_+|hypothetical-protein
MKSQRKLPVLAAIAVLMLAITACGGNTPAEAPGEPSPTASPSPAESAASPSPSPAAQPSSSPAEESQVIQGTGIYVGQIDNHSVEIKTEEGATSFELGTGLEEAPEALSMDDPVVFEYVERSVEGDSSVLQRVLSKLEKSADSGSAAPSQAALPKSKSFSLTLEGMKEEKTAALAAGNGYSLYVFDIFTFDAKTGRLAMKVDPEYYAEITKLPSDFDLDSLKQEGEKELSSTGKVTALDQKERDRRMSGIRLYLTAMGNGLTREYAVKEIAGQGYVIRLNIPQREASEGFGPHVYTSLDSLVSQ
>NZ_LN831776.1|WP_046506735.1|2665869_2666508_-|hypothetical-protein
MKIDIGCGSGKETGYLGIDRTAWPGVDIICDINEGIPLPDNTAEFVMASRVLPYVNNLFAVMAEIYRISIHKAVICILAPYAHSFPHLSNPLFKQKFDEYTPRYFTGSFFQPAAGAVSPEIPDYPAPVPPFDYRLLRMELFYQYPFDDTLYEAEELEILKTLQSNVVHEIMYHFVVVKKPVTLEELADMSRKTYPEPQALLKRRRHTQNRQV
>NZ_LN831776.1|WP_144412097.1|2658996_2665719_-|DUF11-domain-containing-protein
MKIIPLVVRATINATGAITFTGNTLGLSRSDTTGVPGTQDSIGAFATVNTASVFGTYPAGTTSLYQNNSSSAILTIPSGSTVLYAELIWGGSYINGSVNLSSAINNPVSFTTPAGTTSSVSPDSATSNSVDLGNGALAYVRSANVTSIIQAGGAGTYTTGGVVGTIVITGDSTANHAGWTLGVIYQNPSLPFRNMSLRAGAVLVQASSAPVATTITGFATPVSGALGGRILFSAQEGDANRSGDQALFGPTSNTQVALSGPNNFANNFFASQINNDTGALNTTGTFGTRNQTNGSPGTNIIGGRQGWDITNVDVSARLVNNQSSALLTLTTSGDAYVVNGNALQIDINAPKISLTKGSNVAGTVVGDTVTYTVTVSNTGTASATSAVLSDTLPAGLTFVNRSVVVAGVYRPSYDITAGVPLGTLTLGTSATVTYQATVTSLPAPQTVANTANVAFTFQSVAGGPIVTGVIPSNTDTLPVYSPVLGIVKSASTANATVGDQITYTLQITNTGNIGAATVITDNIPAGSSYVPGSFTVNGTPTAGNPSTGISIGTVPAGGSTTVQFQVQVNSLPSPPQLVDQATAAYTFLVPDGRTLAGTAASNTLTIPVALPNVAVVKSAGFTDAAVGDILLYTSVISNNGIAPVTNVVLSDPVPAGSSFVPESVSVAGAARPSADPATGITVGTVAAGTSVTVTFQVNVTSVPSPAQLSNRSSASYSSGVFTGISQSNTTVTPVYQPVITIVKSASTASATVGGNVLYTLRVQNTGNLAAAVVLSDNIPAGSAFVAGSVTVNGVARPSDSPTGGIALGAVAAGAAVTVTFLTAVQSLPSPPVLNNQGSSSYTYQLPSGRSLSGASLSNTVSLPVSAPGITLLKNASLASMAVGENLTYTVAVSNPSGVSVNNVILSDPVPAGASFVAGSVTVNGASLPSANPGAGISLGTIAAGATSTVAFQVNAALLPNPAVFTNKASASFTAGAFSGTALSNTVSTSVYIPVINLVKSANAAQASVGSSLSFTILVSNTGNIAAVLNLTDALPPQAVFETNSVSIGGTPLPGYSPAAGIPVGPLAPGDSVPVSFLVTVTALPPNQQLLNSAAASFTFTLPDGRQLGGNAASNTLAVPVSAPNVSIVKSVNAIDAVTGDILTFTSVLTNNSIAAVSHIILSDPLPENAAFIPGTVIVGGVSQPLSVPSAGIPIGSLGPEASVAVTFEVRITMPIPSQINNQSTVSFTSGVFSGSSSSNITSTPVIQPQISLVKSANALNATVGDTVIYTVAVSNAGNLAANVTLTDNIPAGTVFDPNSVIVGGFPQPGTAPDTGITVGTVAPGASIPVSFTVIIVSLPSPQQLVNQAASTFTYTPPDGRLLTGTAVSNTVTVAVSAPNVAVVKSTTATAAALGDTIPFSVNITNTDAEPVNSVQLSDPTPPGTTFVTGSVSVNGVPFTNANPATGVSVGTIAPGASANVTYNVTVTSAPASAAINNQATVTYTSGVAFSGSTISNTVSVPFYQPVLSAVKSASTANATVGDTVTYTLTVSNTGNYPAALTVKDTIPAGTAFQPNSVLINGLPLPQADPAAGIAAGTIAAGATVAVVFSVVITSLPSPQLLVNQGTAAYSFTLPDGRTLNGSVLSNTVTIPVTNPNLAVVKTTATTATTLGDTIVYSVTLTNNGIAAVNNVVFTDALPSGTAFVPGSVLVNGVARPAASPSTGITIGSIAPGASVTVAFSVTVNSLPGSGLLNNQSSVSFTSGALSSVAFSNIVTTPVYQPVIGAAKSASTVKATVGDTIIYTVNVSNTGNYPATATLTDTIPAGSTLVPNSVLINGFPSPGANPATGIALGTIAAGTTLAVTFSVVIDTLPVSQQLSNQATVSFAFTLPDGRTFNQAAVSNINQISVSAPNVQVVKSSPATDAVIGDTVTYSITVTNNGIEAITNAVLSDPVPAGASFASSSVVVDGTPLPGANPANGIALGTIAPGASSLVTFSILVNALPASGTLSNQASVSFTSGAFSGASYSNTFVTPVYQPFINIVKGADTANATVGDTVTYSLKVTNTGNLAANVTITDSIPAGAVFIPNSVLVNGVPQPGADPASGLNIGTVAPGATITVTITLQVTVASLPSPQQLVNQAAATFTFSPPDGRLLSGSSESNVLVIPVSSPDVTAVKSTPAVDAVVGDIITYTIAVTNNGIESVNNVVLVDPIPAGSQFVAGSVTVDGVPRTGANPAAGIVIGTITPGDSVTVTFQVQVIAV
>NZ_LN831776.1|WP_020428220.1|2657323_2659000_-|DUF11-domain-containing-protein
MIRDSRLQPVVSNQSMVLYSSAAGADVITYSNTVNTPVVGPVLTLVKSADHTSASLGETLVYTLIARNEGNAPALTTLVDALPSGVSFVANSVLRDGVPLPGVSPFSGILLGAVAPQTEVRIAFQVIVVSLPPSLELGNRARAVYSFTTPEGRHVEGEVFSNQITVSLLAYKLSILLASSTPTTFVGDAVTFTLRVRNEGTRLMSGILTTLPVPEGAIFLPGSVISGGIYSPDADPDKGIPLPPLDPGKTADISFQVRVVSVPALTAQAVVTYDADGDTDGTKSNTVTVAVIQSGLSVSLKVDKYSAAPGDRLGYRFTIRNSGKLAVDAMLAGAIPSGTLFVWDSVHIDGIPQRGVHPGEGIPLGTIRAGSAAVVDLLVSIPAEADILQMPAIQNQGSVEYTFTLPDGRNVRERVRSNTVTTLLFSPVISIEMTGEPPMVEPGGIAEFNIAVTNSGNYPAEVSVIQIIPQGCTLETGKVTISVHTVPESKYSGIVSLGVMDPGQTAQLSYLVRVHPGYMGSALQGSSTALYLYTIDGRRYSGEARSNSYKLMIEEISE
>NZ_LN831776.1|WP_046506732.1|2656051_2657212_-|sporulation-protein-YhbH
MPQSSGHSAFVVSKEDWSLHRKGHQDQERHQQKVREAIKDNLPDLVTEENIIMSDGKQIVKVPIRSLDEYRIIYNFRKQKHVGQGDGESQVGDVLGRDSQSAHPGKGDKAGDQPGQDTVEAEVDLEDLEDILFEDMELPHLAPKTQEEIEVKSIVFNDIRKKGMMSNIDKKRTLLENLRRNASRGKPGIHSISPDDLRYKTWDDITVPHSNAVIIAMMDTSGSMGTFEKYCARSFFFWMTRFLRRQYEKVEIVFLAHHTEAKEVSEHDFFTRGESGGTICSSAYQKALDIIDSRYPPAKYNIYPFHFSDGDNLTSDNERCVKLIGELLKRSNMFGYGEVNQYNRSSTLMSAYRHLKQEQFMHYVIKDKKEVYQALKTFFGKREAVK
>NZ_LN831776.1|WP_020428216.1|2654292_2655798_+|alpha-glucosidase/alpha-galactosidase
MSFKVAFIGAGSIGFTRGLLRDLLTVAEFKEIEVSFMDINPHNLQMVNELCQRDIRENGLKIVISATTDRKEALKDAKYVFCTIRMGGLEAFATDVDIPLKYGVDQCVGDTLCAGGIMYGQRGIAEMLEICRDIREAAAPDVLLLNYSNPMAMLTWACNKYGGVRTIGLCHGVQHGHQQIAEVYGLEKSEVDIICAGINHQTWYISAKHKGRDLTGGLLEAFEKHPEFSRTEKVRIDMLRRFGYYSTESNGHLSEYVPWYRKRSGEIMDWIDLGSWINGETGGYLRVCTEGRNWFETDFPNWMKDPALEYTSEHRGEEHGSYIIEGLETGRVYRGHFNTVNNGIITNLPDDAVIEAPGYVDHNGISMPVVGDLPLGPAAVCNVSISVQRLAVEAAVHGDDKLLRQAFMMDPLVGAVCNPKEIWQMVDEMLVAGEAWLPQYSAAIAEAKVRLASGDLVPTLADNAGAARLKVKSVDEMMQDREAANKNAGESDKGKDREKVR
>NZ_LN831776.1|WP_020426763.1|2671269_2671731_+|DNA-starvation/stationary-phase-protection-protein
MAKASNKVTTTSLEQVLNREVANLNVLYVKIHNYHWYVKGEQFFSLHVKFEELYDDVTLKMDEVAERLLSIKGSPAATMKEYLELATIQEATGKEDTRGMVQTLIEDFATVAEELTEGIELAEQVSDQPTADLFIKIRSDLEKNQWMLRSFLG
>NZ_LN831776.1|WP_020426762.1|2672011_2672794_+|Fe-S-cluster-assembly-ATPase-SufC
MAADFVIEGLKATIEGKEILKGINLQMKGGEIHAIMGPNGTGKSTLASALMGHPKYEVTEGTAVLEGEDLLEMAVDERARAGLFLAMQYPSEISGVTNSDFLRSAINSRREEGNEISLIRFIRQMEAKMKELDMNPEFLHRYLNEGFSGGEKKRNEILQMMMLDPKIVILDEIDSGLDIDALKIVAEGVNSMRSPERGFLVITHYQRLLNYIKPDFVHVMMQGRIVKSGGPELAERLEAEGYEWVKEELGIEDETVGQEA
>NZ_LN831776.1|WP_020426761.1|2672821_2674123_+|Fe-S-cluster-assembly-protein-SufD
MTTQTILPVDAQLLTDWSQSSGEPGWLKDSRLNALTLAAGLALPKLEKTRIDRWNVNNYGTYKAGQTITALSEAPASVAALIKDQEEGSLIIQRNSGAIYVRLAPELAAQGVIFTDLQTAVKEHGDLVQRYLHKAVLPDEHSLAALHAALWNGGVFLYVPKNVVVETPLQAVLLTDDAEAAFVPHILIVADTNSSVTYVDNYVSDKTEAGLHNGAVEVFVGAGAKVRYATVHQLGEDTTDVTYRRAVVENDGTIEWIVGEMNYGDTASDTKSVLKGNGASSDAKVIAVGSGSQKLNYTTQAQHFGKNTPSDMITRAVMRDAATSIINGITKIEKGATRADGQQTEKVLMLSPQARGDANPILLIDEDDVTAGHAASVGQVNYEQVYYLMSRGISRHDAETLIIYGFLAPVVSQIPLEGLRNQLQSLVERKLGQ
>NZ_LN831776.1|WP_020426760.1|2674119_2675346_+|cysteine-desulfurase
MISSAIREQFPILNQTINGHPLVYLDSAATSQKPRQVIEAVKSYYEWDNSNVHRGVHTLGSRATDAYEGAREKLAKFINARSTKEIIFTRGTTTALNIVASSYGPGNVGEGDEIVITQMEHHSNFIPWQQLAKKTGATLKFIPLQKDGSITLEDAEQTITDKTKIVAIAYVSNVMGISHPVKELAAIAHRHGAVIVVDGAQSTPHMKVDVQDLDCDFYALSGHKMLAPTGIGALYGKKALLEAMEPVEFGGEMIDDVGLYDSTWKELPWKFEGGTPIIAGAVGLGAAIDFLQEIGLDEIHRHEMELAAYAEQRLSEVDGLTIYGPRNRKVGVVTFNLGDVHPHDVATVLDAEGVAVRAGHHCCQPLMRWLQVSSTARASFYLYNSEQDVDALVQALIKAKEYFGYELG
>NZ_LN831776.1|WP_020426759.1|2675332_2675773_+|SUF-system-NifU-family-Fe-S-cluster-assembly-protein
MNLDDLYRRVIMDHYKNPRNRGSFADDALKIELNNPTCGDRITLQLKVEDGVVKDARYSGEGCSISMSSASMMTEAVKGQTVEHALELADRFSSLMKGEAVDFEDYEDIEALSGVNKFPARIKCATLAWNALRKGIDVEEEHHQEH
>NZ_LN831776.1|WP_020426758.1|2675792_2677190_+|Fe-S-cluster-assembly-protein-SufB
MAKKAPDMEEYQYGFRDEHKSIFQSGKGLTAEIVKEISAIKNEPEWMLDFRLKALEQFYKMPMPKWGGNLDELDFDDIQYYVRPSEKQGKTWEEVPSEIKETFDKLGIPEAEQKFLAGVSAQYESEVVYHSMQKNLEDQGVIFTDTDTALREHPELFKKFFGTIIPPADNKFAALNSAVWSGGSFIYVPKGVKCEVPLQAYFRINSENMGQFERTLILADEDSFVHYVEGCTAPIYSTNSLHSAVVEILCMKNARVRYTTIQNWAPNIYNLVTKRAVAEENATMEWVDGNIGSKLTMKYPAVVLKGRGAKGSVLSIAVAGKDQHQDAGAKMIHLAPDTTSTIVSKSISKHGGKVTYRGLASFGRKAEGAKSNIKCDTLILDNQSTSDTIPYNEIMNDNIVLEHEATVSKVSEEQLFYLMSRGLTEAEATQMIVMGFIEPFTKELPMEYAVEMNRLIKFEMEGSIG
>NZ_LN831776.1|WP_167345606.1|2677670_2677931_+|hypothetical-protein
MTTPQFIQWLESKMEEHGHKKVIPNDAVLQSKLQDEAKQILRQRLAQKLLTEAGFENQFETALGVLSEAVGEYSELLRETPLLTIT
>NZ_LN831776.1|WP_081487111.1|2678518_2678629_+|divergent-PAP2-family-protein
MYDAAGIRRHAGMHAALLNQISNNFSQITKGEAPAV
>NZ_LN831776.1|WP_046502276.1|2679283_2680750_+|HAMP-domain-containing-histidine-kinase
MSIRLKFLLSYAAMLIVPLLLLLLTASLLTIVYHGDVQSLKSAYENKFEGMEERDTRNLIKHTFMQNTDLLTDTVFLDDLSADMLKKNTSLFIRSDQKTMYASKGLLLEQGLLDELPAFKNAGVHEEPFRKKYNNNWYQIAQFDLLSKASEPVSIFLISKTDPLVHFVRTFFPILFLSTVVVLLLTHTLLTTYMSRKIIHPLLELREAAGLVTEGNLDFRVKIDSKDELGQLGMAFEEMRSRLQQSLLMQQQYESNRKELITNISHDLKTPITAIKGYVDGILEGVADSPEKNEKYMRTIAAKAGEMDHLIDELFLFSKLDMQKLPFSFESVPILPFLKDWAEELEVELEKQQVDLQIDMNGGEAARISVDRDSFKRVLGNIIQNSLKYMDKPEKRITVQTLVEGKNFTLAIGDNGPGIPPEAAGHIFERFYRAEQSRNTNTGGSGLGLAIARQIILEHGGTIHADSKEGEGTEIRIVLPIEEGGAGE
>NZ_LN831776.1|WP_020426753.1|2680746_2681436_+|response-regulator-transcription-factor
MKRTILIVEDEPSIAELQRDYLEMNGYQTEIAVNGEQGLELSLSGKFELIVLDVMLPKLNGFEVCKRIRGELDIPILMVTARREDIDIVRGLGLGADDYMTKPFKPAELVARVKAHLSRYDRLKGRGSSTSELEIRGLRLNPDSRRAFIRDEEVSLTTKEFDLLYFLAQHPNHVFSKDQLFERLWGVDSLGDTQTVTVHIRKLREKIEEDSANPLYIETLWGAGYRFRS

Crispr_ID: NZ_LN831776_36

• CRISPR_ID: NZ_LN831776_36
• CRISPR_location: 2809420-2809494
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: RT

Consensus repeat of NZ_LN831776_36

Consensus_repeat	Method
AATTAGTGTCCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_36

>36.1|2809443|29|NZ_LN831776|CRISPRCasFinder
CATCTGCTCGAGGATAGGGTACTCCGGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_36

CRISPR arrays

The CRISPR arrays of NZ_LN831776_36

>merge|NZ_LN831776|36|2809420-2809494|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTTCATCTGCTCGAGGATAGGGTACTCCGGCAAATTAGTGTCCCTTTTTCCACTT

>NZ_LN831776|36|38|2809420-2809494|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTT	CATCTGCTCGAGGATAGGGTACTCCGGCA
AATTAGTGTCCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_046502372.1|2809912_2810356_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046506771.1|2805512_2807297_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_085981582.1|2797953_2798637_+|HAD-hydrolase-like-protein	unknown	unknown	gnl|CDD|136007
NZ_LN831776.1|WP_020429211.1|2823186_2824752_+|glycoside-hydrolase-family-43-protein	unknown	unknown	gnl|CDD|350129
NZ_LN831776.1|WP_020428784.1|2807293_2808613_+|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_LN831776.1|WP_046502378.1|2815553_2816438_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_046502375.1|2812753_2813767_+|glycosyltransferase	unknown	unknown	gnl|CDD|340832
NZ_LN831776.1|WP_046502367.1|2802567_2804712_+|hydantoinase/oxoprolinase-family-protein	unknown	unknown	gnl|CDD|223223
NZ_LN831776.1|WP_020428765.1|2794988_2797085_+|alpha-galactosidase	unknown	unknown	gnl|CDD|269892
NZ_LN831776.1|WP_081487232.1|2810909_2811995_-|YheC/YheD-family-protein	unknown	unknown	gnl|CDD|373047
NZ_LN831776.1|WP_020427294.1|2818410_2819745_+|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	gnl|CDD|275209
NZ_LN831776.1|WP_020428774.1|2799749_2801099_+|FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|378963
NZ_LN831776.1|WP_141639110.1|2804724_2805396_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_144412099.1|2801214_2802507_+|TRAP-transporter-large-permease-subunit	unknown	unknown	gnl|CDD|225407
NZ_LN831776.1|WP_039788503.1|2797486_2797744_+|AbrB/MazE/SpoVT-family-DNA-binding-domain-containing-protein	unknown	unknown	gnl|CDD|131898
NZ_LN831776.1|WP_046502384.1|2820751_2822986_-|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_020427290.1|2813881_2815414_-|DUF3502-domain-containing-protein	unknown	unknown	gnl|CDD|378792
NZ_LN831776.1|WP_020427293.1|2816450_2817431_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_LN831776.1|WP_020428772.1|2798988_2799735_+|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_046502381.1|2820192_2820495_+|hypothetical-protein	unknown	unknown	unknown

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831776.1|WP_020427294.1|2818410_2819745_+|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	1.8e-45	149.8	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_046506771.1|2805512_2807297_+|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	1.25003e-51
NZ_LN831776.1|WP_085981582.1|2797953_2798637_+|HAD-hydrolase-like-protein	gnl|CDD|136007	PRK06698, PRK06698, bifunctional 5'-methylthioadenosine/S-adenosylhomocysteine nucleosidase/phosphatase; Validated.	1.25997e-38
NZ_LN831776.1|WP_020429211.1|2823186_2824752_+|glycoside-hydrolase-family-43-protein	gnl|CDD|350129	cd18617, GH43_XynB-like, Glycosyl hydrolase family 43, such as Bacteroides ovatus alpha-L-arabinofuranosidase (BoGH43, XynB). This glycosyl hydrolase family 43 (GH43) subgroup includes enzymes that have been characterized to have alpha-L-arabinofuranosidase (EC 3.2.1.55) and beta-1,4-xylosidase (beta-D-xylosidase;xylan 1,4-beta-xylosidase; EC 3.2.1.37) activities. Beta-1,4-xylosidases are part of an array of hemicellulases that are involved in the final breakdown of plant cell-wall whereby they degrade xylan. They hydrolyze beta-1,4 glycosidic bonds between two xylose units in short xylooligosaccharides. These are inverting enzymes (i.e. they invert the stereochemistry of the anomeric carbon atom of the substrate) that have an aspartate as the catalytic general base, a glutamate as the catalytic general acid and another aspartate that is responsible for pKa modulation and orienting the catalytic acid. Also included in this subfamily are Bacteroides ovatus alpha-L-arabinofuranosidases, BoGH43A and BoGH43B, both having a two-domain architecture, consisting of an N-terminal 5-bladed beta-propeller domain harboring the catalytic active site, and a C-terminal beta-sandwich domain. However, despite significant functional overlap between these two enzymes, BoGH43A and BoGH43B share just 41% sequence identity. The latter appears to be significantly less active on the same substrates, suggesting that these paralogs may play subtly different roles during the degradation of xyloglucans from different sources, or may function most optimally at different stages in the catabolism of xyloglucan oligosaccharides (XyGOs), for example before or after hydrolysis of certain side-chain moieties. It also includes Phanerochaete chrysosporium BKM-F-1767 Xyl, a bifunctional xylosidase/arabinofuranosidase. A common structural feature of GH43 enzymes is a 5-bladed beta-propeller domain that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	7.70028e-172
NZ_LN831776.1|WP_020428784.1|2807293_2808613_+|sugar-ABC-transporter-substrate-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	4.68956e-75
NZ_LN831776.1|WP_046502378.1|2815553_2816438_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.44639e-52
NZ_LN831776.1|WP_046502375.1|2812753_2813767_+|glycosyltransferase	gnl|CDD|340832	cd03802, GT4_AviGT4-like, UDP-Glc:tetrahydrobiopterin alpha-glucosyltransferase and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. aviGT4 in Streptomyces viridochromogenes has been shown to be involved in biosynthesis of oligosaccharide antibiotic avilamycin A. Inactivation of aviGT4 resulted in a mutant that accumulated a novel avilamycin derivative lacking the terminal eurekanate residue.	1.96648e-77
NZ_LN831776.1|WP_046502367.1|2802567_2804712_+|hydantoinase/oxoprolinase-family-protein	gnl|CDD|223223	COG0145, HyuA, N-methylhydantoinase A/acetone carboxylase, beta subunit [Amino acid transport and metabolism / Secondary metabolites biosynthesis, transport, and catabolism].	7.39344e-68
NZ_LN831776.1|WP_020428765.1|2794988_2797085_+|alpha-galactosidase	gnl|CDD|269892	cd14791, GH36, glycosyl hydrolase family 36 (GH36). GH36 enzymes occur in prokaryotes, eukaryotes, and archaea with a wide range of hydrolytic activities, including alpha-galactosidase, alpha-N-acetylgalactosaminidase, stachyose synthase, and raffinose synthase. All GH36 enzymes cleave a terminal carbohydrate moiety from a substrate that varies considerably in size, depending on the enzyme, and may be either a starch or a glycoprotein. GH36 members are retaining enzymes that cleave their substrates via an acid/base-catalyzed, double-displacement mechanism involving a covalent glycosyl-enzyme intermediate. Two aspartic acid residues have been identified as the catalytic nucleophile and the acid/base, respectively.	1.557e-90
NZ_LN831776.1|WP_081487232.1|2810909_2811995_-|YheC/YheD-family-protein	gnl|CDD|373047	pfam14398, ATPgrasp_YheCD, YheC/D like ATP-grasp. A member of the ATP-grasp fold predicted to be involved in the modification/biosynthesis of spore-wall and capsular proteins.	1.79065e-94
NZ_LN831776.1|WP_020427294.1|2818410_2819745_+|group-II-intron-reverse-transcriptase/maturase	gnl|CDD|275209	TIGR04416, hypothetical_protein, group II intron reverse transcriptase/maturase. Members of this protein family are multifunctional proteins encoded in most examples of bacterial group II introns. These group II introns are mobile selfish genetic elements, often with multiple highly identical copies per genome. Member proteins have an N-terminal reverse transcriptase (RNA-directed DNA polymerase) domain (pfam00078) followed by an RNA-binding maturase domain (pfam08388). Some members of this family may have an additional C-terminal DNA endonuclease domain that this model does not cover. A region of the group II intron ribozyme structure should be detectable nearby on the genome by Rfam model RF00029. [Mobile and extrachromosomal element functions, Other].	2.99651e-138
NZ_LN831776.1|WP_020428774.1|2799749_2801099_+|FAD-dependent-oxidoreductase	gnl|CDD|378963	pfam12831, FAD_oxidored, FAD dependent oxidoreductase. This family of proteins contains FAD dependent oxidoreductases and related proteins.	2.78015e-146
NZ_LN831776.1|WP_144412099.1|2801214_2802507_+|TRAP-transporter-large-permease-subunit	gnl|CDD|225407	COG2851, CitM, H+/citrate symporter [Energy production and conversion].	0.000755683
NZ_LN831776.1|WP_039788503.1|2797486_2797744_+|AbrB/MazE/SpoVT-family-DNA-binding-domain-containing-protein	gnl|CDD|131898	TIGR02851, stage_V_sporulation_protein_T, stage V sporulation protein T. Members of this protein family are the stage V sporulation protein T (SpoVT), a protein of the sporulation/germination program in Bacillus subtilis and related species. The amino-terminal 50 amino acids are nearly perfectly conserved across all endospore-forming bacteria. SpoVT is a DNA-binding transcriptional regulator related to AbrB (See pfam04014). [Regulatory functions, DNA interactions, Cellular processes, Sporulation and germination].	5.76599e-16
NZ_LN831776.1|WP_046502384.1|2820751_2822986_-|AraC-family-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	4.7019e-24
NZ_LN831776.1|WP_020427290.1|2813881_2815414_-|DUF3502-domain-containing-protein	gnl|CDD|378792	pfam12010, DUF3502, Domain of unknown function (DUF3502). This presumed domain is functionally uncharacterized. This domain is found in bacteria. This domain is about 140 amino acids in length. This domain is found associated with pfam01547.	1.19543e-33
NZ_LN831776.1|WP_020427293.1|2816450_2817431_-|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	2.21951e-95
NZ_LN831776.1|WP_020428772.1|2798988_2799735_+|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	5.89073e-57

Protein sequences

>NZ_LN831776.1|WP_020428784.1|2807293_2808613_+|sugar-ABC-transporter-substrate-binding-protein
MKMRTWLLGLIFAVLLAGGCSTGAGNGTHGPEAGAGGRSDGAAAAQEPVKLKFSIWGNDAQKAMYESLIGKFEQLHPGTEVEIMTIPFADYQQKLSIMLASRTAPDAGWLAERMIPQLLESGQLVDIAAEVKDDPGYNYPDIYPSTLDIFNRGGSLYGIPFSTPPVLIYYNKDLFRSKGLKTPTELYKEGHWNYDEFLKAARSITNPQQGIYGVKLVRDWNNWSDALLPLFWSHGAELFDSDGSAFALNSPEGREALQLYSDLMFKDKVHPLPGDELSFDSGQIGMYTDRYSYTSKARAVTDFEWDIAPMPAGIKGTGTSLGYAGVSVFETRHPAEAAEFLKFITSAESMSVTAQYFVPSRKSVLESDVFLRAAAKPSPESIQLAVLDQMADARIAPGHKNWQQIDTKIQMLLDELYTQSATANEVLGKMEVEVNRLMK
>NZ_LN831776.1|WP_046506771.1|2805512_2807297_+|sensor-histidine-kinase
MSKKSIYVPLRTKFIVLFCLLITVPFLVIGAISYKKYTAGVERSTVELSYQVVNQININLEHYIKELDRLTLMPLYDEDVMHILQSHSGSGSASTYLTTDETLKMNLFISSLAFDRGEIESILVFTNDGGIFSNLDQSVRKRWDRSMAEWMGSVKQEDGGLAIIPPHNAAYYTEPKQGIISVARVIREPYTNKMLGIVKVDLTPQGFGSILSTVRLGGSGLLQITGKDQVMLYSAAAGLPDSSESYITASAQSAYTGLKVTSLIPRTQLREDARELTNSTLIVSIIALMAAYAAAILLSNRLIKPIAHLQSKMRQVKRGLFRERATVTTNDEIGQLTEGFNTMIGEIDRLVKEVYETRLKEREAELLALQSQIHPHFLYNTLEMVNMLALQGSTRELSGVVTSLGKLLRYTVGRQDPMVYVLDEVKFVEAYLKIQGMRLGDKLQAVIHMDSSFDYCLVPKLILQPLIENVIEHAMGPDTVHLALTAAVQEDDLILSVKDDGIGISGERMKELEEQLYRDKSRSVPESEPGGFGRIRKGFALRNVHQRLRLLYGEPYGLYIDNTAERGVTISLRLPMHWEALNNAEPAGERQEGA
>NZ_LN831776.1|WP_141639110.1|2804724_2805396_+|hypothetical-protein
MMKTATRTLPSDQVLGYAELKNDLLFHRIPSSKRRYYVERPLAIGREKALEYKARYGTDVGAICRDRGIRVSLNERQGTIGQIRFRAQIELSSQERVITLYKSSMEELRQCAGVLLPGRSFSLQEVTDIHLAHELFHDLEFTELGYTNKRLDDISSLSLGPLRIRASVAKTSEIAAHAFSCHLLGLPCLPNLLDFAYMIHSGTLTAAEFWQEMERCSEALENG
>NZ_LN831776.1|WP_046502367.1|2802567_2804712_+|hydantoinase/oxoprolinase-family-protein
MGNKQIRIGIDVGGTFTDAVAIDNETFEVLSKVKMPTTHHDERGVASGIVQIIQRIMSENGIQPEDIKFIAHGTTQATNALLEGDVARVGILGMGTGLDARSARSETNVANIELAAGKYLTTYHKFIDSKELTREAIDDAIEQLLAEGAEVIVASEAYSVDDPANELRVIEAARSRGVYATGGHEISQLYGLKTRTRTAVVNASLIPKMMETANMTEQAVKEAGITSQLMIMRCDGGVMSIDEVRKRPILTMLSGLAAGVAGALMYEKISDGIFFEVGGTSVDISVIKNGKVMIENAQVGGHKTYLRSLDVRTLAVAGGSMIQIGAGKITDVGPRSAHIAGLEYECFTGKENLQQPSIGLVSPRKGDPDYVTVRGAEGHEYALTLAGAANLLNHVPDEDYARGNMESTRIAWEALGAHLGMSAEEAARAAMDIAIRKVMAVVNQMISDYELDTGFITLVGGGGSGAVLVPAMAAKEGFKHQIANNAPYISTIGVGMAMVREQIEKTVVGATERDIKLIRAEIMEKIVQSGANESTVDVTIEIDSQRNILRAIATGSTELRSKDLASREVPVNELVLTAAEALGQPAERTELKAASGRWFLFESSEVKKSMFGLVKKKLSHVGVLDREGVVRFKKTNAYHLAFLKKNIDDRFASFLEENTVYSDANATIPKTFIFYKEKMLDLTGMQTKEQLFSILEVETQLLEDNSEMLAVVYQ
>NZ_LN831776.1|WP_144412099.1|2801214_2802507_+|TRAP-transporter-large-permease-subunit
METVQIIGILLVFIVFVGLMMTRKLTTLLALPMMAILLAAIAGIPLLSDNPDTFTITKGVLAGGAMKLSTAIAGLIFGAWFGQILNKVGITKTIIRKAAELAGDKPLAIAIIFFLAASVIFSAANGLGMVILVGTIAIPIMLTAGLKPFVSGLVVLLANAVGVVFNVSTWAIYTDVLKVPTDTIASYSLICAVPLIVIALIMIVYYTRKDGKVRRAWAMPLKQEFQNQDTKNVRSIALLSPLVPVLLVFFLKVDIVSAVFMGALVTLLLATPKRPIHVLSSALVEGIQDVAGALGLMIGIGMLLSAVTAPQVASLIQPLIEGMIPTSPLMYILVFTLLSPLAIYRGPLNVWGLGSGIAALIVAGGMAPVAAMLALRIVSNLQAVSDPTNSHNVWISDYTKTDIIETLRKTLPWMFVAVLISMVIAGLVAF
>NZ_LN831776.1|WP_020428774.1|2799749_2801099_+|FAD-dependent-oxidoreductase
MRKYDVVVAGGGVSGSIAGIAAARAGAKTLIVEAGGFLGGTLTAAGVGPMMTFHAGHKQAIQGITDELVQRLRALGKSPGHIADATNYTYSVTPFDAEAMKLELDLMLQESGGEVLYHTMLAGAEVSDRRIRSLTLCNKAGLSRITADVFIDATGDGDLAVWSGVPFTKGREADEQSQPMTLKMKMRGVDTGKIKAYIREHREDFPRMNLDITVMDSAARLSVIGFDKQFREAKVRGEISIPREDVLFFETSNPGEIIMNTTRILGKDSTDPWSLSEAEIEGRKQCRELEIFLKKYIPGFEEAVVVSTGPSIGVRGSRQIKGVYTLTAQDILAKRPFEDVIAHSGYPIDIHSPDGEGTATEHLEWGAMYGIPYRCLITNEIDNLIVVGRCLSATFEAQAAVRTTPTVGAIGQAGGTAAALAAKGGVPVQEVDTGRLQQTLVAHGAYLEL
>NZ_LN831776.1|WP_020428772.1|2798988_2799735_+|response-regulator
MHKLFLVEDEALIRSGLKHLVEEVIGGFKVVGEAENGRLALEALKSIKPDVLITDIRMNEMNGLEMIRRIRDQYPDLYILILSGYADFEYAKQAIKYGISDYLLKPVDRTELAQALGEFKRKHGSGGDISDSTGEGGTDNKGRQLIRKVKELVAQRLDQEISLQYMAEQVHLNHQYLSVLFKSETGQNFTDYVSQCRMNRAKQLLKETNLKIYEVAKLSGYLSSKHFMAVFKDYTGRTPSQFREDKTY
>NZ_LN831776.1|WP_085981582.1|2797953_2798637_+|HAD-hydrolase-like-protein
MSTKLKKPEAIIFDMDGTLFQTESLLLPAYHKMFDILRAEGLYAGPTPPEERILSSLGMLLSQIWKNVMPDADEAVHRRADELLLQLEVEGLEAGGTLLYPKVTETLVALHERGVKLFVASNGLEDYIHSIVVVHELKELFDGLYSAGGQGTATKTELLRILLDEHGIKEAWMVGDRSSDVEAGKGNGQTVIGCAYAGFGRQDELKGSDVIISSFDELIGLYDNSTV
>NZ_LN831776.1|WP_039788503.1|2797486_2797744_+|AbrB/MazE/SpoVT-family-DNA-binding-domain-containing-protein
MMKATGIVRKVDELGRIVIPIELRRTMGIDIKDPLEIFVDGEKIILRKYEPTCIFSGSAENLINFKGKMVSKDVLDELIASFDRV
>NZ_LN831776.1|WP_020428765.1|2794988_2797085_+|alpha-galactosidase
MDSKRIDIAENGLYLTIEITGEQDVRLLHFGAAPLQDGSIAEKNKPGFRLLELQLSGEDRDEYHGRTHRASYPGLRMVYGGHSDSVNALGRKLEITLTDPVTGITAVQHLQFYTGVQTVRCWTVLKNTGTGEAAVEYVSTFALTGVDKEGSGDRNDKIEVTIAHSGWQSELQWRTYRLPELGMSHLADRGSKRIAASNTGSWSAAELLPMAVLHNKESGTSLFWQIEHNGSWHWELTDQYDQLTLLVSGPTEHDNHWWLKLAPGEEFTSVPVAVGAVQGGFQGAAEQLTAYRRMIRRPNEDNELLRIIFNDYMNCLWGSPTTGKLLPLIDAAADVGCEYFCIDAGWYAPGEWWDGVGQWEPSAERFPEGIKYVLDYIRSKGMIPGLWLELEVMGINSPKLTETDDSWFFMRHGKRVKDRSRYQLDYRNPKVIAHADGVISRLVEQYGVGYIKMDYNINAGIGTETDADSFGDGLLQHNRAYLAWLDSIFARYPNLVIENCSSGGMRMDYAMLSRHSIQSTSDQEDYVQYAAIAAGSPAALTPEQSAVWSYPLREGDDEEVIFNMVNALLLRVHQSGHLAELEPRRRELVKEALDYYKSIRAHIPQATAFWPLGLPDSEGEWVSFGLRHGDTRYLAVWRIAGEAAAVKLPIPELQGQAAGVSCAYPQRHHSDWSWNPSEGVLTVSIPQGKTARLFEIHA
>NZ_LN831776.1|WP_046502372.1|2809912_2810356_+|hypothetical-protein
MKSIKTVLQAILYVLLAVGLHLILIYFLKIRIEGWGTELLKYSFKVYFVPLLLCFINSFLCIRTKRLKYHVNWFLVTMIPSFLLILFFKAIQGVGDSEYGVVVSIEFFPKYQVEMLFLLPWSISIIQFILTLYYLIKIRKEVNRLKV
>NZ_LN831776.1|WP_081487232.1|2810909_2811995_-|YheC/YheD-family-protein
MHFHVNKIKSRLSRSYIHVYNERVIVFTPGDVHVSKDQIHALVYDVKSGTWSRKWRSFPNMIYDRCRIQRSKRFEQLLRFRARYGHLTFLNRPLRNKWTVYQTFLQKSRFRQHMPETLLYQSSADLHRILKSSPVVYIKPASGTGGRGILRIERLKEGKSLYDIQGRRLSRQIIAPRKVPLTRLESIVHQWCLGGRFLVQQGIPLRLSSGRYHDYRMLVQKNGQGVWELTGMAGRVGAARSVTSNLHGGGHAIRAEILLKQWLGSQEKAEKAMKTAEKLGLDAAAYLEESFGTLCELALDLAINREGQIYVLEVNPKPAREVFSRSGDSSTYRKALTRPLEYAMWVYKNKNAPSPAKVVGD
>NZ_LN831776.1|WP_046502375.1|2812753_2813767_+|glycosyltransferase
MKKLIKLPESRKLTIAQVISNYPNAQPVPSIKGGTEKIVYELTEELVRRGHKVYLFAALGSRSRAKLITYPKGLRHESIARFVLKKLPERVDIIHDHTFRSALGVTNPKVPTVCTVHIPVKRRIKYPVYVSKRARRLMGNNKGFCVYNGINTREYEFSTEKHLYLLYIGRIIRNKGVMQAIQVAEKTGKRLIIAGPVKASRFFEREVKPRIRNNPNIQYVGPVGGKMKQQLLKHAECVLFPTLWEEPFGLVLIESLGCGTPVLALRNGAVPEILSGFPNLICNNISEMAVKVRQKRYPSPHLLRAYVQKHFTNKQMTDSYLRIYHEVIQRESGRKKF
>NZ_LN831776.1|WP_020427290.1|2813881_2815414_-|DUF3502-domain-containing-protein
MKKKKGWLSLLLAAGFLVGGCSQGNNESAAPSSGSGNEGTPSVTDNGSKDGSPLAPAKLKIVLYGDESNRMKELAKTEFYDVIKKEINAEVEFHFLPWTEYGGGKTDLMLSTGEDFATYTDANYMVKSVAKGLYADLTPYVSAAADLSKNVDEASFKAFQLDGKQYAIPVGNKPNSAEFYSALVRQDLLEEAGMTQVTSLKELEQFYDKVHAIHPELIGYANTDARRILQYDYTDKNLYWQNDFIALDESAKDDKIISWFETEEFKKYANLMRGWYEKGIIPKYAATNVPQLQSDWNSGKAMFWAGTAARPFEGAATISQAVPEAKLVNYFLGSGRPKISRGTYSTAFFVSTAAKDPERYVMFFNLLQKNQELYDLFAYGIKGTDYTVDENGRLTKINTDSLIPDWLLMNKNFIRFDNTVPDEFIAEYKAWDDGAIISKGAGFNFDNTPVKNEETKLNGVFTEYLAPIGSGFSDYDTAFPKALDRLKAAGIDKYIAEYQKQFSEWYAKQK
>NZ_LN831776.1|WP_046502378.1|2815553_2816438_-|carbohydrate-ABC-transporter-permease
MQTTENKGLLIFFYCCIAIFSAICLVPFILAVSGSLSTESRIAAEGYSFWPRGFTFETYEFLFGSKAQQILRAYSMSVIVTVLGTVSAVLVTTAYAYVISVKSFRLKNFFAFFAYFTMLFSGGTLPWYLLSTKYYHLGDTLIGLFIPYVLSVFLMFLMANYFRSIPHEIVESAQIDGAGHLRIFFSIMIPLGRVGLVTISLFYALQFWNDFYLPLMLVTDQKLYTIQYLMYNMMANIQFLASGNAAQVGGAIIAPPLETAKMAMTCLTVLPIAILYPFLQRFFVKGIIVGSVKG
>NZ_LN831776.1|WP_020427293.1|2816450_2817431_-|sugar-ABC-transporter-permease
MMQEATPETQGRLSPGIRTARAKSFRKSLKKDSTLYLLALPGIVILILFAYLPMSGLILVFKNYNFNDGIFGSPWAGFSNFEFFFSSMEDSLRATRNTVMLNALYMLTGTFFSVAIAIILNELRSKWFIKITQSVMFFPYFISWIIIGAILFSLLDYDKGIMNQLLQTLGISQVDWYSSPWLFVIILVLANIWKSAGYGAIIYYAVLQGIDTSYYEAAKIDGASRWQIITRITVPMLIPSIILMTLLGIGGMLKGDLSMIMGVTFLNPLLLPTTDIIDVYVYRTAIRSGEFGFASAITLYQSVFGFLLVLVANKLAGWYDKDSKLF
>NZ_LN831776.1|WP_020427294.1|2818410_2819745_+|group-II-intron-reverse-transcriptase/maturase
MDTKLSRIAEVARNRPKERMTSLVHLLDKQRLWDCHLEMQGDKAAGVDGVTKAEYERELESNLEDLLSRMKRQAYKPKPSRRTYIPKENGNKRPLGIPSYEDKLVQKAMSQILNAIYEEKFLPCSYGFRPGRSQHQALQALDRLIMKQGVRYIVDVDIKGFFNYVDHEWLRQFLEHDIADPNFLRLIGRFLKGGVMEEGFYQETEEGTPQGGNLSPLLGNVYLHYVLDLWFEIEIKGKRCRGKAGMVRFADDFVCGFEREEEAKAFYEALEERMGKFNLTIAEEKTKLIRFGYGAEVDCKRAGLTKPATFDFLGFRHIWGRGKSGKYRLLRKTSPKKFRLRVKEITQWARQNRHQPEGMFVDSVRRKLRGHYQYYGVSDNWHGISRYYSLVLNAIWKWRNRRSQKRTFTLEKFKAFLARNPLPKPRITVNLYATVNGNLKSRMP
>NZ_LN831776.1|WP_046502381.1|2820192_2820495_+|hypothetical-protein
MDEFLTNSGRNAVVEEPKAGLAINNGRNTVVRVAKVGLAINSGRYTVLEAAGSVWPYPENYKAEESAALDFLIPTSACSPASSQALVGKRELIFPKIKKS
>NZ_LN831776.1|WP_046502384.1|2820751_2822986_-|AraC-family-transcriptional-regulator
MGKRKKLYTRFFMSLTAISVCCILVLAVVIFYWYRNITIDNVNKANQNVLVNTETVFINYKEIVQNYAMDFYRNPNINALMMNGDTSWSDQLYSALSQIRGALVVNQYMENAYIMGVNEPVAMFENLPLSPESKLELFSRMRNNVIVESPFLWKATLNNGTPITLLTVFYNDRAFADSEYYGAVALTVNLGKLQNNLFTQKEGEITRYAVLDGNASVLMHSALSGTPLEEDMLKQVVASSPERGSFVYRGSGEPQLITYVYSAADKLWFVSETSYKDSIRDISNARTLMTGLCLALIIAAALTANLISRRMYKPIGRLFGNIVHLSGNEEALKTGGDFDTVSQELEQIGVKLEQLKKESDDSALMRWLLSPRGTPENSSTPMMSIAASGGAYCVCVLTLLESGQSEGSGQTFGEGIEQIELAFSELAAVQSFRPHQGTAVLILSELRSGSFDDYALFRGKWEDIAARLQHSDVSCALGISGLTDDLHLLRAKYNEAADSLQYIKFHVQQNIIFADDTIHLNSSPMPDSALEPVLQAVRQTELSGHIPQAVERLLAVACSYRAESATIALARLAFELSRTAELNADVQQSGFLDNYQRIWQLQSYDKLLHWIVDSCYTALKRIASMSAVQTKSIAVEAICYIRDHYDDSRLSLNALADKLSLSPAYLSRLIADEVNCSFPDFVNLLRLEQAQMLLVTELDLDIREIAEKVGYNSSTYFTTQFKKRFGITPSKWRMNHILQKQESS
>NZ_LN831776.1|WP_020429211.1|2823186_2824752_+|glycoside-hydrolase-family-43-protein
MRTFRNPVLPGFYPDPSAIRVGEDYYLVTSSFEFFPGVPIFHSKDLVNWRQLGHVLDRPSQLNLDHTIPSMGIWAPTLRYHEGVFYMITTYVDNDKNQHNFYVTATDPAGDWSDPVWLEDAPGIDSSLFFDDDGKVYYTGNRVPPEGQDYPKHMDIWLQEIDLSQGRLIGPKHSIWQGALKVAHAQEGPHIYKIGAWYYVLIAEGGTGHTHAITIARSKSVTGPYEGHKANPILTHRHLGRAYPIVNVGHGELVETQHGDWWMFCLASRTCGGYYRNLGRETFLTPVIWENEWPVVNPGKGVLELETPAPDLPETRWPELPARDEFTGSELGLIWNFLRTPRGEFWSLTEKPGFLRLHLKAERLSEIANPSFIGRRQQHLSFRAAADMTFRPAAEGEVAGLVLLQNADYHFRYEYGLEAGERVLQLIQRKGGSEQLLASVPYPQDQVQLKVEARGQEYSFYYRSSEAAKWTAFFERADGRVLSTDLAGGFTGAYIGMYTSSQGAESESYADFDWFSYEGLE

Crispr_ID: NZ_LN831776_37

• CRISPR_ID: NZ_LN831776_37
• CRISPR_location: 2868027-2868102
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_37

Consensus_repeat	Method
AAATTAGTTACCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_37

>37.1|2868051|28|NZ_LN831776|CRISPRCasFinder
AACCTGCGGGAGAACAGGGTAATCGGGC

CRISPR arrays and Neighbor proteins around NZ_LN831776_37

CRISPR arrays

The CRISPR arrays of NZ_LN831776_37

>merge|NZ_LN831776|37|2868027-2868102|CRISPRCasFinder
AAATTAGTTACCCTTTTTCCACTTAACCTGCGGGAGAACAGGGTAATCGGGCAAATTAGTTGCCCTTTTTCCACTT

>NZ_LN831776|37|39|2868027-2868102|CRISPRCasFinder
AAATTAGTTACCCTTTTTCCACTT	AACCTGCGGGAGAACAGGGTAATCGGGC
AAATTAGTTGCCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020427952.1|2881676_2882405_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_LN831776.1|WP_046502436.1|2876152_2879194_+|alpha-amylase	unknown	unknown	gnl|CDD|200459
NZ_LN831776.1|WP_167345609.1|2860774_2861218_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020428507.1|2861558_2862674_-|sporulation-integral-membrane-protein-YtvI	unknown	unknown	gnl|CDD|274334
NZ_LN831776.1|WP_020427955.1|2872794_2873436_-|5'-deoxynucleotidase	unknown	unknown	gnl|CDD|378993
NZ_LN831776.1|WP_039839884.1|2866766_2867192_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427960.1|2868599_2869469_+|glucose-1-dehydrogenase	unknown	unknown	gnl|CDD|235853
NZ_LN831776.1|WP_025707777.1|2860325_2860724_+|FxsA-family-protein	unknown	unknown	gnl|CDD|236913
NZ_LN831776.1|WP_020427959.1|2869871_2870474_+|thiamine-phosphate-synthase	unknown	unknown	gnl|CDD|181086
NZ_LN831776.1|WP_020428512.1|2859795_2860329_+|acyl-CoA-thioesterase	unknown	unknown	gnl|CDD|223894
NZ_LN831776.1|WP_046502429.1|2871644_2872757_+|2-iminoacetate-synthase-ThiH	unknown	unknown	gnl|CDD|236425
NZ_LN831776.1|WP_020428504.1|2865703_2866645_+|malate-dehydrogenase	unknown	unknown	gnl|CDD|180477
NZ_LN831776.1|WP_020428517.1|2857692_2858436_-|hypothetical-protein	unknown	unknown	gnl|CDD|240449
NZ_LN831776.1|WP_020428514.1|2858554_2859736_+|MFS-transporter	unknown	unknown	gnl|CDD|340893
NZ_LN831776.1|WP_020428505.1|2864317_2865613_+|NADP-dependent-isocitrate-dehydrogenase	unknown	unknown	gnl|CDD|180792
NZ_LN831776.1|WP_020428506.1|2863063_2864176_+|citrate-synthase	unknown	unknown	gnl|CDD|184467
NZ_LN831776.1|WP_039787644.1|2879522_2881316_+|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|380161
NZ_LN831776.1|WP_020427957.1|2870849_2871614_+|thiazole-synthase	unknown	unknown	gnl|CDD|234687
NZ_LN831776.1|WP_020427954.1|2873539_2875213_+|fumarate-hydratase	unknown	unknown	gnl|CDD|377546
NZ_LN831776.1|WP_020427958.1|2870540_2870744_+|sulfur-carrier-protein-ThiS	unknown	unknown	gnl|CDD|169065

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020427952.1|2881676_2882405_+|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	1.07233e-85
NZ_LN831776.1|WP_046502436.1|2876152_2879194_+|alpha-amylase	gnl|CDD|200459	cd11320, AmyAc_AmyMalt_CGTase_like, Alpha amylase catalytic domain found in maltogenic amylases, cyclodextrin glycosyltransferase, and related proteins. Enzymes such as amylases, cyclomaltodextrinase (CDase), and cyclodextrin glycosyltransferase (CGTase) degrade starch to smaller oligosaccharides by hydrolyzing the alpha-D-(1,4) linkages between glucose residues. In the case of CGTases, an additional cyclization reaction is catalyzed yielding mixtures of cyclic oligosaccharides which are referred to as alpha-, beta-, or gamma-cyclodextrins (CDs), consisting of six, seven, or eight glucose residues, respectively. CGTases are characterized depending on the major product of the cyclization reaction. Besides having similar catalytic site residues, amylases and CGTases contain carbohydrate binding domains that are distant from the active site and are implicated in attaching the enzyme to raw starch granules and in guiding the amylose chain into the active site. The maltogenic alpha-amylase from Bacillus is a five-domain structure, unlike most alpha-amylases, but similar to that of cyclodextrin glycosyltransferase. In addition to the A, B, and C domains, they have a domain D and a starch-binding domain E. Maltogenic amylase is an endo-acting amylase that has activity on cyclodextrins, terminally modified linear maltodextrins, and amylose. The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues (Asp, Glu and Asp) performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase.	4.43757e-158
NZ_LN831776.1|WP_020428507.1|2861558_2862674_-|sporulation-integral-membrane-protein-YtvI	gnl|CDD|274334	TIGR02872, UPF0118_membrane_protein_YtvI, sporulation integral membrane protein YtvI. Three lines of evidence show this protein to be involved in sporulation. First, it is under control of a sporulation-specific sigma factor, sigma-E. Second, mutation leads to a sporulation defect. Third, it if found in exactly those genomes whose bacteria are capable of sporulation, except for being absent in Clostridium acetobutylicum ATCC824. This protein has extensive hydrophobic regions and is likely an integral membrane protein. [Cellular processes, Sporulation and germination].	7.04855e-72
NZ_LN831776.1|WP_020427955.1|2872794_2873436_-|5'-deoxynucleotidase	gnl|CDD|378993	pfam12917, HD_2, HD containing hydrolase-like enzyme. This is a family of bacterial and archaeal hydrolases.	5.36765e-93
NZ_LN831776.1|WP_020427957.1|2870849_2871614_+|thiazole-synthase	gnl|CDD|234687	PRK00208, thiG, thiazole synthase; Reviewed.	4.90298e-142
NZ_LN831776.1|WP_020427960.1|2868599_2869469_+|glucose-1-dehydrogenase	gnl|CDD|235853	PRK06701, PRK06701, short chain dehydrogenase; Provisional.	0
NZ_LN831776.1|WP_025707777.1|2860325_2860724_+|FxsA-family-protein	gnl|CDD|236913	PRK11463, fxsA, phage T7 F exclusion suppressor FxsA; Reviewed.	1.8946e-33
NZ_LN831776.1|WP_020427959.1|2869871_2870474_+|thiamine-phosphate-synthase	gnl|CDD|181086	PRK07695, PRK07695, thiazole tautomerase TenI.	1.3797e-76
NZ_LN831776.1|WP_020428512.1|2859795_2860329_+|acyl-CoA-thioesterase	gnl|CDD|223894	COG0824, FcbC, Predicted thioesterase [General function prediction only].	2.24597e-35
NZ_LN831776.1|WP_046502429.1|2871644_2872757_+|2-iminoacetate-synthase-ThiH	gnl|CDD|236425	PRK09240, thiH, 2-iminoacetate synthase ThiH.	0
NZ_LN831776.1|WP_020428504.1|2865703_2866645_+|malate-dehydrogenase	gnl|CDD|180477	PRK06223, PRK06223, malate dehydrogenase; Reviewed.	0
NZ_LN831776.1|WP_020428517.1|2857692_2858436_-|hypothetical-protein	gnl|CDD|240449	cd13426, Peptidase_G1, Peptidases of the G1 family, including scytalidoglutamic peptidase and aspergillopepsin. Some members of this family had been classified earlier as carboxyl peptidases insensitive to pepstatin, and the family has also been called the eqolisin family, due to the fact that the conserved catalytic dyad of the family consists of a glutamate (E) and glutamine (Q) residue. The family is found in fungi and bacteria.	1.22316e-49
NZ_LN831776.1|WP_020428514.1|2858554_2859736_+|MFS-transporter	gnl|CDD|340893	cd17335, MFS_MFSD6, Major facilitator superfamily domain-containing protein 6. Human Major facilitator superfamily domain-containing protein 6 (MFSD6) is also called macrophage MHC class I receptor 2 homolog (MMR2). It has been postulated as a possible receptor for human leukocyte antigen (HLA)-B62. MFSD6 is conserved through evolution and appeared before bilateral animals. It belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.9038e-47
NZ_LN831776.1|WP_020428505.1|2864317_2865613_+|NADP-dependent-isocitrate-dehydrogenase	gnl|CDD|180792	PRK07006, PRK07006, isocitrate dehydrogenase; Reviewed.	0
NZ_LN831776.1|WP_020428506.1|2863063_2864176_+|citrate-synthase	gnl|CDD|184467	PRK14034, PRK14034, citrate synthase; Provisional.	0
NZ_LN831776.1|WP_039787644.1|2879522_2881316_+|HAMP-domain-containing-protein	gnl|CDD|380161	NF033092, HK_WalK, cell wall metabolism sensor histidine kinase WalK. This model describes WalK as found in Staphylococcus aureus (sp|Q2G2U4.1|WALK_STAA8). A shorter version, as found in Streptococcus pneumoniae, called WalK(Spn) or VicK, is not included. WalK is part of a two-component system and works with partner protein WalR.	6.4132e-107
NZ_LN831776.1|WP_020427954.1|2873539_2875213_+|fumarate-hydratase	gnl|CDD|377546	pfam05681, Fumerase, Fumarate hydratase (Fumerase). This family consists of several bacterial fumarate hydratase proteins FumA and FumB. Fumarase, or fumarate hydratase (EC 4.2.1.2), is a component of the citric acid cycle. In facultative anaerobes such as Escherichia coli, fumarase also engages in the reductive pathway from oxaloacetate to succinate during anaerobic growth. Three fumarases, FumA, FumB, and FumC, have been reported in E. coli. fumA and fumB genes are homologous and encode products of identical sizes which form thermolabile dimers of Mr 120,000. FumA and FumB are class I enzymes and are members of the iron-dependent hydrolases, which include aconitase and malate hydratase. The active FumA contains a 4Fe-4S centre, and it can be inactivated upon oxidation to give a 3Fe-4S centre.	5.57798e-92
NZ_LN831776.1|WP_020427958.1|2870540_2870744_+|sulfur-carrier-protein-ThiS	gnl|CDD|169065	PRK07696, PRK07696, thiamine biosynthesis protein ThiS.	7.20915e-22

Protein sequences

>NZ_LN831776.1|WP_039839884.1|2866766_2867192_+|hypothetical-protein
MDRIFFFLHMIGTLALGFYLVLPFILSGTAKLSASAKEGTLSAIGGFNRFAQYGLVIQLLTGGYMISQGDYTVAWMVVVVVLLLAMFALGGIMGKPLRLAAAGMRENRDVSGHTAKLRTLSLLLMVVLIVMMFFMVYRHII
>NZ_LN831776.1|WP_020428504.1|2865703_2866645_+|malate-dehydrogenase
MAIKRNKITVVGAGFTGSTTALMLAQKELGDVVLLDIPQLENPTKGKVLDMLEAGPVLKFDARITGTSSYEDAADSDIVIITAGIARKPGMSRDDLVNTNAGIVKSVCENVKRVAPESIVIILSNPVDAMTYVAFKTLGFPKNRVIGQSGVLDTARYCTFIAEELNVSVEDVRGFVLGGHGDDMVPLVRYSSVGGIPIETLIPAERIAEIVQRTRVGGGEIVSLLGNGSAYYAPAASLVQMTEAVLKDKKRILPVIALLEGEYGYDGLFMGIPALLGAEGIEKIFELELTAEEKAALDKSADSVRSVTSVVTI
>NZ_LN831776.1|WP_020428505.1|2864317_2865613_+|NADP-dependent-isocitrate-dehydrogenase
MLKLEKYDLPTEGEQITIEDGKLLVPDHPIIPFIEGDGTGRDIWKASKRVLDAAVAKAYGGKKQIAWYEVFAGEKAFNTYGEWLPNDTLEAIREYIVAIKGPLTTPIGGGIRSLNVALRQELDLYVCLRPVRYFDGVPSPVKHPELVDMVIFRENTEDIYAGIEYKEGSAEVKKVIEFLQNELGVNKIRFPETSGIGIKPVSSEGSKRLVRSAVEYAIKHGRKSVTLVHKGNIMKFTEGAFKNWGYEVAEQEFGDKVFTWNQYDAIKEKSGEAAANAAQKEAEASGKIIIKDAIADIALQQVLTRPTDFDVIATLNLNGDYLSDALAAQIGGIGIAPGANINYVTGHAIFEATHGTAPKYADKDVVNPGSVILSGVMLLEHLGWQEAADLIYKGMSTAINNKTVTYDFARQMEGATELKCSAFADEIISHL
>NZ_LN831776.1|WP_020428506.1|2863063_2864176_+|citrate-synthase
MTATKGLEGIVATTSSISSIVDGVLTYRGYDIDDLAEHATFEETAYLLWFGNLPTTPELQALQRDLSAFAPIPEQVIAQMKLYPKEANTMAALRSAVSSLALYDEAADDMSREANEIKAVKLQAQIPTVVAALARIRKGLEPVAPKEGLSLAENFLYMLWGKQPDIVSVKALDAALVLHADHELNASTFAGRVTVATLSDIYSGVTSAIGALKGPLHGGANEAVMKMLEEIGTLDAVEPYIQGKLERREKIMGFGHRVYKNGDPRAKHLMKMSHELGLMKNDTALYDMSVKVEELITSKKGLKPNVDFYSASVYTQLGIERELFTPIFAISRTSGWTAHILEQYEDNRIIRPRAEYTGMSEQKYVPVDER
>NZ_LN831776.1|WP_020428507.1|2861558_2862674_-|sporulation-integral-membrane-protein-YtvI
MDTLVLKRVLRGLWVVLAAALLLLGVYVLLPLVYPLLLAYLLAYLMHPLVLILRGFKLPRWLAVSLSLLFYVGGTALVLTALITRLVKELIGLLQTFDLHTDQWRELLLSISRNASIQNIINQINQFYHDNPDYHATIDSNISRTTETVGQAVTELITGFFNMVLKLISALPSMGSILIVIMLSAFFLSTGWERHNAKLRALVPVPLRRPVSEIWHDLRNALFGYLRAQLVLISITAIIVIAGLLLLGVNSAFAIGLTIGLVDLVPYLGVGIVLLPWAIYSYMTGNLALGIGLSVLYAVILITRQILEPKVLASSIGLDPLAMLIGVFAGLQLFGMPGLLLGPVLLVVLDAFHRAGVFRALHSYIVSGRLH
>NZ_LN831776.1|WP_167345609.1|2860774_2861218_+|hypothetical-protein
MRGKSTFELARCVLNGEMRGKSTSELARCVLNGEMRGKSTFELAGCVLNGEMRGKSTFELAGCALNGEMRGKSTFELAGCAQNGEMRGKSTFELAGCLQGGFVCLGLPKRVSITDSALEEAKLTLINAAPFVDSCTYQACGDTATGI
>NZ_LN831776.1|WP_025707777.1|2860325_2860724_+|FxsA-family-protein
MIRNKWLWAALFVIPAVELFGFIYVAGFLGAPKTLLLMLASSVIGFLMMRFEGKKVLLDSRTHMQEGRVPGKTMLDGLCIFFGGLLLILPGFVTDIVGFSLVFPLTRPLYRVFLLKWIEKKMKNGTFTFYRR
>NZ_LN831776.1|WP_020428512.1|2859795_2860329_+|acyl-CoA-thioesterase
MKSRNPVLTSRWHGTTFRVRYQETDQMGVVYHANYLSWFESGRTEMFRELGFAYRSLENMGVLLPVTTADLQFKSPARYDDLVAVYARLTTFSALRVVYEYEIRRLAGTETGDPEAFGLAGGSAPADVEQLPGELLVTGSTSHVWLNTDWKPVRLDRVLPELFLAITMALREEGGAV
>NZ_LN831776.1|WP_020428514.1|2858554_2859736_+|MFS-transporter
MKKLLKLRGFYLFLGLAGGSFGSYLTLLLKQGGLDSGRIGMLMATGTLIAICIQPLWGVISDRYNQARLVLILSVAVPAVLAVFYQSEYFIVLLVVYTLSTIFSSTQAPIADSYAIVAANKAGSTYGSIRMMLSIGAAVGAYAGSQYVSHFSVSTIWVPFLLLSSVAVVFALTLPKQAEENRMMSQSFSKGIKTLLGNKIFLAFLGGSFLVNQTMTAFGTYFVLAFQSVGGSTSHAGIALFIASFTNFPSMLYASKVIKKLGRERTLLLGALIYVLRWGIQFAFPTPGVMIGVQVLHGLSFGLFYVAAVEYVSHITLPEMQATGQSVFNIVFSGFAGILGNLLNGILLREGGVWLMNLSCMLSSALGVLLIFYVSRSTRKRILIPVASERASL
>NZ_LN831776.1|WP_020428517.1|2857692_2858436_-|hypothetical-protein
MNRADLSKRTRPCVTDKVHSGKAQSTGFGWTSGNWSGYAISGKKGAFQRITGEWIVPLVKPTSNPTYSSAWIGIDGFKNSSLIQTGTGHESTKGVVHYYAWWEILPAAETVIPLPVSPGDHMKASIVKLGSGKWSITLSNLSKSWTFRTFQRYTGPQTSAEWIMEAPQVGGTIGKLAQVSATRFFRCRVNGRSPKLTPADGGIMVQKKITVSVPGSPNASGDAFIVKRVYRKGKPLIHSRSPIIVRS
>NZ_LN831776.1|WP_020427960.1|2868599_2869469_+|glucose-1-dehydrogenase
MPDNKQSTKTLPPQVQDRQPGIESEMKPRPEFETSSYKAAGKLLGKAALITGGDSGIGRAVAVHFAKEGADVVISYLNEHADAEETKRQVEQEGRKCILVAGDIGVEAFCQDLINKTVEGLGKLDILINNAAEQHPQDKIEDITSEQLERTFRTNIFSMFYLTKAAMPHLKKGSTIINTTSITAYRGSPQLLDYSSTKGAILSFTRSLSMNLAEKGIRVNAVAPGPIWTPLIPSTFDAKKVSEFGGTQPMKRPGQPEELAPAYVYLASEDSSYVSGQVMHVNGGEIVNG
>NZ_LN831776.1|WP_020427959.1|2869871_2870474_+|thiamine-phosphate-synthase
MAEIHLISDGKLEPGRFINLAAAVYPLVDYIHLREKHRPALELLDMAKQLLLAGVPASSLVINDRLDVALAAGAGAVQLAWNSLPPASARAAAPGLRLGRSVHSAAEAAEAGRHGADYGLFGHVFPTACKPGQQERGLGLLAEAVRRSRMPLIAIGGIEPGNAAQVIRQGAAGIAVMSGICSTEDPVAAARAYRLAVREA
>NZ_LN831776.1|WP_020427958.1|2870540_2870744_+|sulfur-carrier-protein-ThiS
MNLIINGKALEIAEDCRTVADLLSRPEWSGRLVIVERNGEIVNREHYAGTSFSEGDRLELVHFVGGG
>NZ_LN831776.1|WP_020427957.1|2870849_2871614_+|thiazole-synthase
MLDPLVIGGITLSSRLFIGTGKYSRNTLIPEVVASSGSQVITVALRRVDPESRDNIVSHIPPHMTLLPNTSGARTAGEAVRIARLARAAGLGNWVKIEVINDQKYLLPDNLETIRATEILAAEGFVVLPYMSPDLSAAIRMKEAGAAAIMPLGSPIGSNRGLRTKELLRILISEVDLPVIVDAGIGRPSEAAEAMELGAAAVLLNTAIATARDPLLMAEAFREAVSSGRKAYLAGLGPVEENAVASSPLTGFLK
>NZ_LN831776.1|WP_046502429.1|2871644_2872757_+|2-iminoacetate-synthase-ThiH
MSFYESLTRLEQLPYESLWQQFQVEDVKRALCKDRLDESDLLALLSPAAEPCLEEIARRAQRLTRTHFGHVMQLFTPMYLADFCVNHCTYCSFSSIYDFPRKRLTPEEVRQEAIAIASTGLRHLLVLTGESRSASPASYVKECVEILHEYFPSVSIEVNPLSTAEYRELREAGVDGLTLYQEVYHQETYRKLHVKGPKRVFRNRLDAPERGCQAGFRAVNIGALLGMYDWRQEAFMTAMHARYLQDKYPECEIGLSAPRFRPYLGEFNPDSDVTDRALVQIILAYRLFLPRSGITLSTREPAPLRNHLIHLGITKMSAGVSTEVGGHTQDGGTPQFEISDERSVEEITDMLQANGLQPVFKDWDLLGLQA
>NZ_LN831776.1|WP_020427955.1|2872794_2873436_-|5'-deoxynucleotidase
MNYHFSAYLYRLQYIQRWSLMRSTAPENVAQHSFQVALLSHMLCSIGNVHFARSLNADRAAAMALFHDATEVFTGDIATPVKHNNPRLLSSFRDMERIAAERLIGMIPPELSSVYAPLLQPQDSPSGSEDARLLRYVKAADHLDAYLKCVWEVAAGNREFAAAKVQTAAKLRGLEMPEMEYFLAHMAPGFELSLDELSAGAGGGQALEDEGTP
>NZ_LN831776.1|WP_020427954.1|2873539_2875213_+|fumarate-hydratase
MQHFEDSVYDLIVETSTNLPGDVRRAVAKGRALEDRATRSGLALTTIAQNIGMAELQVSPICQDTGMPTFIIHTPVGVNQIEMKKDIHNAIIRATINGKLRPNSVDSLTGENSGNNLGAGTPVIHFEQWEETGVDVRLILKGGGCENKNIQYSLPAELEGLGKAGRDLDGIRKCILHSVYQAQGQGCSAGFIGVGIGGDRTTGYELAKKQLFREVEDVNPNDDLAKLEEYIMENANKLGIGTMGFGGEVTLLGCKIGVMNRLPASFFVSVAYNCWAFRRQGILVDPSTGHIQEWLYESGTGISVGAEDGAAPAAVLEAVSAAAEGADCGVVSEDAAIPAAPAVLSAAEAEAKLAGKPAEAAAGESREVRLTTPVSEEDIRSLRVGDVVILSGEMHTGRDALHKYLMDHEAPVDLNGAVIYHCGPVMLKDEEGWHVKAAGPTTSIREEPYQGDIIKKFGIRAVIGKGGMGPKTLKALQEHGGVYLNAIGGAAQYYAECIKKVNGVDFMEFGIPEAMWHLQVDGFAAIVTMDAHGNSLHADVEKDSAAKLAQFREPVFK
>NZ_LN831776.1|WP_046502436.1|2876152_2879194_+|alpha-amylase
MKRKLWLIPALITSIVLSITANLFVLPPTQVEAASIGTVTENDTIYQIMVDRFNDGDTSNNATGAAIRYGENSEEDFRYMKGGDWQGVIDKLPYIHNMGYTAIWISPVAEPQVTSRDNNGTGKNTAYHGYNVKNPNAANPYFGTKEKLKELVDSAHALGIKVIIDVVPNHIGDYMLGSQAYYDIPGLQPAAPFNNPAWYHHNGDINWSLADGRYDQWAQDYMENHDLGGLDDLDLDVPAAKQAIFNSIKGWFDYTGADGARVDAAKLIKPTDIGELQNLLGVNTFGENFDGNAEFVSRWVGPNKEWGMLDFPLFFSVLNSFAYGQSFDSNIKSTLAQDSYYNGNANHMVTFIDNHDRNRFLTEAGGNVDKMQNALSFIFTVRGTPVVFQGTEQNKGNGNGQIMTGGIADTWNRWSMVKRDAGGNVLENYFNENTSTYKHIAKLNDIRKNNPALRTGTQREMWSAQNLYAFSRRIDSGTNVGQEVISVFSNASGGSQTVTIPLRAESSLTAGTVLINQLNTSDKVTVQAGGTTGKQITVTVGANSAKIYSKTQPVVDTEAPSVPSNVTATVQNASSVLVNWTASTDNVGVTGYEIYRNGVKVGTSATTSYTDNTVASQTNYSYTVKAFDAAGNLSAFSAAALVTTPAGNNVTIYYKQGYTTPYIHYRPVGGTWTAAPGVAMPAAEVSGYNKITINIGSATQLEAAFNNGSGTWDSNGGSNYLFGTGTWTYTPTGNIKSGGPVTPTTTPTPTPTATPTPTPTATPTATPTPTPTATPTPTPTATPTATPTPTATPTATPTATPTVTPTVTPTATPVGNSVTIYYKNTAFTNSYIHYKLDGSTVWTTSPGEQMQASSYSGYKAATIQLGSAAGLTAAFNNGSGAWDNNGSSNYHFGAGTWSLVNGSIAAGEPQADSVTFRVSVPGTTPANGPLYLTGSFNSWNAADPAYQLTKGSDGVYSVTVSLPAGTAVQYKITRGGWDTVETSSSGADIANRTLTPAGGAQTVNLTVQRWKDQ
>NZ_LN831776.1|WP_039787644.1|2879522_2881316_+|HAMP-domain-containing-protein
MRPFRIRLTFILMALIGISMIGAGITMAKLFKDSHISALEENMSREINLLSGTFQFTDTDSPGAVSYYTEQAEHIAKLTNSRITFITKDGKVIGDSEKNPLEMDNHSTREEEVLAAKEGIGRAIRYSDTLNREMLYVAGAVVSDQGFDGYIRLSMALDAVTEGLNRAWMVMAGGLVLLFIAATFVSYKVASGMTSPLEQITRVARRITDLDYDARVPMNRRDEIGQLATAINAMADSLQAQLKTIRDNEDLLQSVLDNMTGGIVMINAEGEIALLNRAAEQLLDVKNSEMAGHSFKELKHHYELSRLIEEGVSRNEAVHEERSIYNPTERIVRLDGVPMIQDGSNRGMLFLLQEVTEIRRLEKMRSEFVANVSHELKTPVAAVKGFAETLLGGGVKDEKTARSFLQIIYDENERLNRLIGDILELSKIESKRAQLECSPVHLIEFFDSLLETLSKVAEKKNISLNASVPEELFMEGDEDKLRQIFINLISNAINYTQDGGSVNVNVVNGQKADGTETVVFTVRDTGMGIPRKDLPRIFERFYRVDKARSRSSGGTGLGLSIVKHLVELHHGSISVESDLGIGSSFILELPLLQDEPH
>NZ_LN831776.1|WP_020427952.1|2881676_2882405_+|response-regulator-transcription-factor
MAQRLLVIEDEPTLSRLLSYNLTQEGYEVTVEDHGTAGYDRAAREPFDLIVLDLMLPGMNGIDILDKLRSQGIRTPVIVLTAKNAEEDVVRGLKSGADDYITKPFGVSELLARVSAVLRRISGLAEEVQPEAAVSASTIILGQLEIYPERYEVSLGGQSINLRPKEFEVLLYLARKPGVVLTRDDLMNAVWGFDYIGGQRTVDVHVSSLRKKLELDPESVHIDSIRGVGYKLVVNKKRTPVI

Crispr_ID: NZ_LN831776_38

• CRISPR_ID: NZ_LN831776_38
• CRISPR_location: 3064863-3064937
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_38

Consensus_repeat	Method
AATTAGTGTCCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_38

>38.1|3064886|29|NZ_LN831776|CRISPRCasFinder
CATCTGCCCGAGGATAGGGTACTCCGGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_38

CRISPR arrays

The CRISPR arrays of NZ_LN831776_38

>merge|NZ_LN831776|38|3064863-3064937|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTTCATCTGCCCGAGGATAGGGTACTCCGGCAAATTAGTGTCCCTTTTTCCACTT

>NZ_LN831776|38|40|3064863-3064937|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTT	CATCTGCCCGAGGATAGGGTACTCCGGCA
AATTAGTGTCCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020427491.1|3071950_3073090_-|class-I-SAM-dependent-RNA-methyltransferase	unknown	unknown	gnl|CDD|223194
NZ_LN831776.1|WP_020428153.1|3058932_3059373_+|DUF86-domain-containing-protein	unknown	unknown	gnl|CDD|225293
NZ_LN831776.1|WP_046502585.1|3061990_3063199_+|LysM-peptidoglycan-binding-domain-containing-protein	unknown	unknown	gnl|CDD|349448
NZ_LN831776.1|WP_020427496.1|3066765_3067872_-|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_LN831776.1|WP_081487145.1|3067871_3068660_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_LN831776.1|WP_020427489.1|3073936_3075154_-|MFS-transporter	unknown	unknown	gnl|CDD|340949
NZ_LN831776.1|WP_020426768.1|3063701_3064004_+|heme-biosynthesis-protein-HemY	unknown	unknown	gnl|CDD|223393
NZ_LN831776.1|WP_020428152.1|3059465_3060128_+|transcriptional-regulator	unknown	unknown	gnl|CDD|225222
NZ_LN831776.1|WP_020427497.1|3065787_3066612_+|aldo/keto-reductase	unknown	unknown	gnl|CDD|381383
NZ_LN831776.1|WP_046502602.1|3065453_3065771_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046502589.1|3063324_3063576_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020428150.1|3060945_3061752_+|glutamate-racemase	unknown	unknown	gnl|CDD|234851
NZ_LN831776.1|WP_046502609.1|3068791_3069667_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213231
NZ_LN831776.1|WP_020428156.1|3057642_3058227_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197775
NZ_LN831776.1|WP_052741444.1|3069663_3071259_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020428151.1|3060230_3060707_+|YtxH-domain-containing-protein	unknown	unknown	gnl|CDD|378938
NZ_LN831776.1|WP_020428155.1|3058425_3058713_+|Dabb-family-protein	unknown	unknown	gnl|CDD|214884
NZ_LN831776.1|WP_020427490.1|3073286_3073916_+|O-methyltransferase	unknown	unknown	gnl|CDD|226607
NZ_LN831776.1|WP_020427492.1|3071255_3071870_+|DUF4097-family-beta-strand-repeat-protein	unknown	unknown	gnl|CDD|226123
NZ_LN831776.1|WP_020426769.1|3064045_3064285_+|DUF1450-domain-containing-protein	unknown	unknown	gnl|CDD|377806

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020427491.1|3071950_3073090_-|class-I-SAM-dependent-RNA-methyltransferase	gnl|CDD|223194	COG0116, COG0116, Predicted N6-adenine-specific DNA methylase [DNA replication, recombination, and repair].	1.46232e-155
NZ_LN831776.1|WP_020428153.1|3058932_3059373_+|DUF86-domain-containing-protein	gnl|CDD|225293	COG2445, COG2445, Uncharacterized conserved protein [Function unknown].	3.09439e-15
NZ_LN831776.1|WP_046502585.1|3061990_3063199_+|LysM-peptidoglycan-binding-domain-containing-protein	gnl|CDD|349448	cd06229, M14_Endopeptidase_I, Peptidase M14 carboxypeptidase family-like domain of Endopeptidase I. Peptidase M14-like domain of Gamma-D-glutamyl-L-diamino acid endopeptidase 1 (also known as Gamma-D-glutamyl-meso-diaminopimelate peptidase I, and Endopeptidase I (ENP1); EC 3.4.19.11). ENP1 is a member of the M14 family of metallocarboxypeptidases (MCPs), and is classified as belonging to subfamily C. However it has an exceptional type of activity of hydrolyzing the gamma-D-Glu-(L)meso-diaminopimelic acid (gamma-D-Glu-Dap) bond of L-Ala-gamma-D-Glu-(L)meso-diaminopimelic acid and L-Ala-gamma-D-Glu-(L)meso-diaminopimelic acid(L)-D-Ala peptides. ENP1 has a different substrate specificity and cellular role than MpaA (MpaA does not belong to this group). ENP1 hydrolyzes the gamma-D-Glu-Dap bond of MurNAc-tripeptide and MurNAc-tetrapeptide, as well as the amide bond of free tripeptide and tetrapeptide. ENP1 is active on spore cortex peptidoglycan, and is produced at stage IV of sporulation in forespore and spore integuments.	1.358e-97
NZ_LN831776.1|WP_020427497.1|3065787_3066612_+|aldo/keto-reductase	gnl|CDD|381383	cd19157, AKR_AKR5G1-3, AKR5G family of aldo-keto reductase (AKR). Bacillus subtilis glyoxal reductase (GR), uncharacterized oxidoreductase YtbE, and Bacillus aryabhattai aldo-keto reductase are founding members of aldo-keto reductase family 5 member G1-3 (AKR5G1-3), respectively. GR (YvgN, EC 1.1.1.283), also called methylglyoxal reductase, reduces glyoxal and methylglyoxal (2-oxopropanal). It is not involved in vitamin B6 biosynthesis.	4.35516e-159
NZ_LN831776.1|WP_081487145.1|3067871_3068660_-|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	1.52834e-73
NZ_LN831776.1|WP_020427489.1|3073936_3075154_-|MFS-transporter	gnl|CDD|340949	cd17391, MFS_MdtG_MDR_like, Multidrug resistance protein MdtG and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This subfamily is composed of Escherichia coli multidrug resistance protein MdtG, Streptococcus pneumoniae multidrug resistance efflux pump PmrA, and similar multidrug resistance (MDR) transporters from bacteria. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. MdtG confers resistance to fosfomycin and deoxycholate. PmrA serves as an efflux pump for various substrates and is associated with fluoroquinolone resistance. MdtG-like MDR transporters belong to the bacterial MdtG-like and eukaryotic solute carrier 18 (SLC18) family of the Major Facilitator Superfamily (MFS) of transporters. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.476e-127
NZ_LN831776.1|WP_020426768.1|3063701_3064004_+|heme-biosynthesis-protein-HemY	gnl|CDD|223393	COG0316, sufA, Fe-S cluster assembly scaffold protein [Posttranslational modification, protein turnover, chaperones].	1.98251e-12
NZ_LN831776.1|WP_020428152.1|3059465_3060128_+|transcriptional-regulator	gnl|CDD|225222	COG2345, COG2345, Predicted transcriptional regulator [Transcription].	6.64182e-58
NZ_LN831776.1|WP_020427496.1|3066765_3067872_-|HAMP-domain-containing-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	2.86899e-48
NZ_LN831776.1|WP_020428150.1|3060945_3061752_+|glutamate-racemase	gnl|CDD|234851	PRK00865, PRK00865, glutamate racemase; Provisional.	1.17818e-124
NZ_LN831776.1|WP_046502609.1|3068791_3069667_+|ABC-transporter-ATP-binding-protein	gnl|CDD|213231	cd03264, ABC_drug_resistance_like, ABC-type multidrug transport system, ATPase component. The biological function of this family is not well characterized, but display ABC domains similar to members of ABCA subfamily. ABC transporters are a large family of proteins involved in the transport of a wide variety of different compounds, like sugars, ions, peptides, and more complex organic molecules. The nucleotide binding domain shows the highest similarity between all members of the family. ABC transporters are a subset of nucleotide hydrolases that contain a signature motif, Q-loop, and H-loop/switch region, in addition to, the Walker A motif/P-loop and Walker B motif commonly found in a number of ATP- and GTP-binding and hydrolyzing proteins.	1.16646e-109
NZ_LN831776.1|WP_020428156.1|3057642_3058227_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|197775	smart00530, HTH_XRE, Helix-turn-helix XRE-family like proteins.	0.000425234
NZ_LN831776.1|WP_020427492.1|3071255_3071870_+|DUF4097-family-beta-strand-repeat-protein	gnl|CDD|226123	COG3595, COG3595, Uncharacterized conserved protein [Function unknown].	0.00124221
NZ_LN831776.1|WP_020428151.1|3060230_3060707_+|YtxH-domain-containing-protein	gnl|CDD|378938	pfam12732, YtxH, YtxH-like protein. This family of proteins is found in bacteria. Proteins in this family are typically between 100 and 143 amino acids in length. The N-terminal region is the most conserved. Proteins is this family are functionally uncharacterized.	6.39795e-11
NZ_LN831776.1|WP_020428155.1|3058425_3058713_+|Dabb-family-protein	gnl|CDD|214884	smart00886, Dabb, Stress responsive A/B Barrel Domain. The function of this domain is unknown, but it is upregulated in response to salt stress in Populus balsamifera (balsam poplar). It is also found at the C-terminus of a fructose 1,6-bisphosphate aldolase from Hydrogenophilus thermoluteolus.It is found in the pA01 plasmid, which encodes genes for molybdopterin uptake and degradation of plant alkaloid nicotine. The structure of one has been solved and the domain forms an alpha-beta barrel dimer. Although there is a clear duplication within the domain it is not obviously detectable in the sequence.	4.06817e-24
NZ_LN831776.1|WP_020427490.1|3073286_3073916_+|O-methyltransferase	gnl|CDD|226607	COG4122, COG4122, Predicted O-methyltransferase [General function prediction only].	3.12504e-47
NZ_LN831776.1|WP_020426769.1|3064045_3064285_+|DUF1450-domain-containing-protein	gnl|CDD|377806	pfam07293, DUF1450, Protein of unknown function (DUF1450). This family consists of several hypothetical bacterial proteins of around 80 residues in length. Members of this family contain four highly conserved cysteine residues. The function of this family is unknown.	4.05839e-08

Protein sequences

>NZ_LN831776.1|WP_020426769.1|3064045_3064285_+|DUF1450-domain-containing-protein
MANDIRICDECNHIKMKSILPKLRKMAPDAEIKTGCISYCGPCGKRPFVYINGRYVSGPTEDEVLAKAEAFVKRPVAKE
>NZ_LN831776.1|WP_020426768.1|3063701_3064004_+|heme-biosynthesis-protein-HemY
MNVKITRNAAKVIKKTMELEGNSELKLRVAITHAHGDHAHYGLDLDTPKENDIVVSTDKEIDVILDPNQPLLDGVKIDYLYFPEEGFVITNPSKGNHGDH
>NZ_LN831776.1|WP_046502589.1|3063324_3063576_+|hypothetical-protein
MKLKKLLSLKQWSHIFRNSWQFVISPQVAMADKLLFTIPVILYWVLPDFMPFLPIDDIGVTMLLTGWFVSRMERKYPALRTGR
>NZ_LN831776.1|WP_046502585.1|3061990_3063199_+|LysM-peptidoglycan-binding-domain-containing-protein
MQQYIARRGDTVSRIAARHGLTPEHVIQGNPWAGRQPYLVPGQILFLPSAPRKRYAVQPGDDAWSIAALFGVDVNELEKLNPGVGSAYGCTPGKMLVIPPAAPHKVVHLRGEYGPAEVEEDIVRLLDQYPFLQHETIGSSVLGKPLHLLRIGSGPHQLHVNAALHANEWLTSPCLLSFVEQYAAAYAEGKGWNGHNPNKWYSNWTVWAVPMANPDGVELVQEGTLPGDPYYDELMAWNGGRRSFRHWKANIRGVDLGDQFPAHWEEEQARRGVPGPGPRDYSGTAALSEPEAAALAQLAERVPGDAAVSLHSQGGEIYWNYRGYEPPESRALAAQLAAASGYRAVELTGSDAGYKDWFIQRFRKPGFTVELGVGKNPLPLADFEDMALETGLILAAILSNFK
>NZ_LN831776.1|WP_020428150.1|3060945_3061752_+|glutamate-racemase
MQQAIAILDSGVGGLTVVKEVMRQLPREKIIYFGDTARAPYGPRSTEEVKMFTEQIVDYLIQFNPKMIVIACNTATAAALDYISAKVSIPVIGVIHPGARAAISATKTGQVGVIGTIGTIKSGAYTAALKQLSPFVQVVSQACPALVPFVEQGMFRSEESHIAVAESLNGIKYEPIDTLILGCTHYPFLVEPIGKVMGPGVKLISSADETAREISTILYDKGKLASGDESPIHQFFCSGDAEMFQRIARDWLGEQIKRTPVVWQVSSL
>NZ_LN831776.1|WP_020428151.1|3060230_3060707_+|YtxH-domain-containing-protein
MKKDTKSLLWGILAGSVVGSVTALLFAPKAGKELRKDIAEGTAEAAHKVQEIAGAASDKGTELYSKAKDAVESVVIEVKEWGRQYTGTDEKKAVEVSGIAAGGDTAEATEANETAETAVEEAAEAVPDEAEARSGAVTGADTVAEEDTANGKAGSGIA
>NZ_LN831776.1|WP_020428152.1|3059465_3060128_+|transcriptional-regulator
MKKGQESGSTRRMIMTLLKMKGPLTIGALAEELGITEMGVRRHVLQLEQEALAKTKVVRQAMGRPLHVYSLTERAEDHFPKSYHNLALELLRELDHGSGQEAVNVLFEGRRKRMLAQYAPMMEKRNLEERVAELSSIQNAGGYMAEWNQEEDGSYVMQEYNCPIRQVATQYRKACQCEQALFEELLGAKVTRTECMAEGGQSCRYAITPRKKDKSPELSV
>NZ_LN831776.1|WP_020428153.1|3058932_3059373_+|DUF86-domain-containing-protein
MYYVNRKQIEIILGQIPDINKGLRAAAASWDGGTFTGLVQERCLHLAIEVVTDVGSSLIDGFIMRDAGSYEDIISIIHEEKVFEGSSLYGLLIQLVALRKPLVQDYYAWDRTSLHPLTAKLPEALEQFAAAVQSYLDQELGTQASV
>NZ_LN831776.1|WP_020428155.1|3058425_3058713_+|Dabb-family-protein
MIKHIVFFKLKDRAPEKVQETVAVLRNMEGKIPQLLSIEVGADIIRSERSFDIALVTVVASLDDLQAYQVHPEHKKVIAHINEVKEVSYAVDYEI
>NZ_LN831776.1|WP_020428156.1|3057642_3058227_-|helix-turn-helix-transcriptional-regulator
MPNNQQEPHKIQAWSLINRKYLGQGVRVKRFRRPKRSQIRNRVLLAVLMAKDIKLSRLAEELSVSSRSVSAWVYEGRIPSRTNLDKVCRTLGYPSHILFNEALLRQSPIVCQPTPSRFMKRANARSPHSNVILTGLCMVYDFSVTDVSIWIGVHPGTFRKWLHQCHLPTLALQEKAENFFHIPRHILFADCELH
>NZ_LN831776.1|WP_046502602.1|3065453_3065771_+|hypothetical-protein
MDQLHFLQLIVSISAEKLNLLYSVHQKMREKQCGPEIPEINCMKYNRRGFKALLLKFCCTKCNHIVCLSGPCPSADFFVYPGAPESWGCAETHGIIEKFSTSEDT
>NZ_LN831776.1|WP_020427497.1|3065787_3066612_+|aldo/keto-reductase
MKHIADVTILNNGIAMPRFGLGTYKAEGEEVARAVATALELGYRSIDTAAVYGNEEEVGRSIAASGVPRDSLFVTTKVWNSDQGYDETLRAFETSSKKLGLDVIDLYLIHWPGMDKYKATWRALERLYAEGRVRAIGVSNFQIHHLEELRKDSETVPAVNQVELHPRFIQKELHDYCASRQIQIEAWAPLMKGRLQDNELLHGIAGKHGKTVSQVILRWGLQNGIVIIPKSVTASRIKENSEIFDFELSAEELSAISGLDAGERIGSDPDKLLF
>NZ_LN831776.1|WP_020427496.1|3066765_3067872_-|HAMP-domain-containing-histidine-kinase
MKTGLRFSVHFVIGLIAWMLGLGITMMISVEVLFPQLGLLEGQEHYDLYILAVFGLNITACSVLFGWYFGSPLRFMMSWIASLSGRNFEPPPALQGIFKRNGKLKFRYRLYGELIVHIESLSAGLKQAELERRKLEDNKKDWVAGISHDLKTPLTYVTGYSALLLNEEYSWNADEQRTFLQEIHAKGRHIEELISDINLSFQMNEDHASLPMQLGTVELIGFLQRLTADVGNDPRAVSHLLSLDAETGPLELVADEKLLYRALQNVLMNAVLHTPAGTAIHVTVRREGDESVNITVSDNGTGMDEDTLNNLFQKYYRGAKNGSPNLGTGLGMAIVKSLILAHGGFLTVESEVSKGTAFHISLPVRQHK
>NZ_LN831776.1|WP_081487145.1|3067871_3068660_-|response-regulator-transcription-factor
MLNLEGTYALRGGTPLLNDHTNAEKILLVDDEKGILTLLEITLKKERYHNISSCTTGEQALFFIKNHTYDLILLDVMLGDANGFELCREIRKHTDTPIFFITSCASDFDKLTGLGIGGDDYITKPFNPLEVIARIKALFRRQSLTQASSSGNPEGAGNKEYNYGRFILRPADASLIVNGESVECTAKELELLSFFCRNPNRIYTTSQIYELVWGSPGYGYEKTVTIHISKIRKKLDDNPKAPELIINLRGIGYKFVPPVKEA
>NZ_LN831776.1|WP_046502609.1|3068791_3069667_+|ABC-transporter-ATP-binding-protein
MELQIEQVSKSYGAKHALSGITLKLKPGVTGLLGPNGAGKSTLMRMLATIEKPTQGRIAWNGVDIAGQPQVLRKELGYLPQDFGVYPNLTPLEFLEYIAAMKGLSARSARTRINELLEILNLANDRKRLLGGFSGGMRQRVGIAQSLLNDPSLLIVDEPTVGLDPGERIGFRNLLSSLSGDRIIILSTHIVTDIESIAPTIALMAKGRLVKYAAPENLIQSVEQKVWNCILPTASLPEMQAKYTVSSAIQRSDGIHTRIVSDLRPSANATLLPASLEDAYLYTVSSLGVQP
>NZ_LN831776.1|WP_052741444.1|3069663_3071259_+|hypothetical-protein
MMRSLSAYFYLIKSNLVSQMRSYSFLFVIGISVFAGYACVPDAAAGYEIFYIGGVRGIYNSAWLGGLAAMLTTMLLWLFGFFMLRSQISGDARLKLGPLIASAPVRKIRYITAKAAANFVVLLVIGAVLLVAFMAMQLLRGESSQLRLTDYMAPFFFVTFPSLFLLGSLTVLFDVFPGLKGVLGNVLFFCLWIAVGVVSIAAPSDWWDLFGVSGILNTMAHSAAEHYPALSSLEGGGSFGYYQTQGQIPTFVWQGAAWDSSLVPVRLVWIAVGIGGIILSALLFRRFEHLEGSAKAHPLAPGREKAPALPLAAMEHSGSLQLSPAVRVKGARLPGRVKAELKLMLKGMSLWWTLPAIILIAAPLLVTANSVNSLLPFIMIWPLALWSQMGTRDQHYFTTGLTLSCSSPLAKWWTEWLSGVFITLLFSAGAIIRFIAEDQMPALLAWGTGLLFIPTLALALGTLGGSKKLFEVIYLLWWYMGPLNHVPSLDFLGVSDRNPVLYLMFTVVLFAAGSAVRLWQTGNLSIRRRTI
>NZ_LN831776.1|WP_020427492.1|3071255_3071870_+|DUF4097-family-beta-strand-repeat-protein
MTKYIRRTWLILIPAAFVMLILAGCGDKAVEKTASFEGSKVQQIEVKTDGQSIQVSRSKDSDVKLRMKTEGELPAVLKAGVLTVSAEPASGFIHLKNETLYLELPEQSYESIRLATASGNITFEDGQAKTILLDADSGNITVTGFAGEIDAATQSGTIHSEVQASAEIQTGGGGQSLKGKVGAESAENSTLSVHSASGNITLEK
>NZ_LN831776.1|WP_020427491.1|3071950_3073090_-|class-I-SAM-dependent-RNA-methyltransferase
MGKLTLIATAPMGLEAVVARELNELGYETAIENGRVLFSGDYIDICRCNLWLRTSDRVLVKMGQFPARTFDELFEGVKAIEWQDWIPENGEFPVEGRSHKSQLTSVPACQGIVKKAIVEKLKLSYRTEWFPENGPRYVVEVILLNDTALITLDTTGPALHKRGYRRQATEAPLKETMAAALIQLSRWNGHRPLYDPCCGSGTLLIEAAMIAWNIAPGLRRSFPSEHWPEIPQRLWEEAREEAFDAVRDDYPLQLTGTDIDPAAIEIAEANAKSAGLAGEITFQAIAAAKARPQGEYGCIITNPPYGERISNDKEVEKLTRQFGEMMLYLPTWSFFAISPYKEFEQYYGRKADKRRKLYNGRIECQYYQYLGPLPPRKPQ
>NZ_LN831776.1|WP_020427490.1|3073286_3073916_+|O-methyltransferase
MPNQEEYSEQLYTEDALLLKVKQAIKDSGMPEVSIAPGYGRLLTMLVAASRSTRILEIGALGGYSGICLCRGLSKAGRLTSLELKAEYAELAGRHLEEAGFGEAVEYKLGPALDSLKLLEAEGRTFDFFFIDADKENYPNYLEYAIKLAAPGAVIAGDNIFLRGRTLNAEKNGPAVQAMRRFNEMIANDERLTSTLLPAYDGLALAVVK
>NZ_LN831776.1|WP_020427489.1|3073936_3075154_-|MFS-transporter
MKNWETWKVNLIVLWFGQFLVNAGMTMITPFLTLYLAKDLGVQGDAIGLWAGLIFAANFMTSFLFQPLWGKLADKYGRKIMLLRSSFGMALVIVLMGFAQTPWQLLLLRLLNGTISGFNPASIALVSGNTPKARMGFAMGLMQSGSVAGTILGPLIGGALADWIGYRPIFYIVGALLFAASLLALFLVKEKFDRAEAAQVPQISVLEGFKELAKVPQLPALFGVTFLLQFAMIAPMTLLPLYVEKLHGSAVDIAFWAGVVSAVTGVSNMLASPVLGKLSDKVGAHRILTYALIGAALFIIPQAFVTSVWQLIIVRFLMGVFMGGLLPSVNALIRSYTPDGKESRAFGFNSSMLALGNMLGAVIGGFLSGFIGIEGLFLISGGFLLINTVWVRLKLYKGAAPRLFR

Crispr_ID: NZ_LN831776_39

• CRISPR_ID: NZ_LN831776_39
• CRISPR_location: 3315087-3315161
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_39

Consensus_repeat	Method
AATTAGTGTCCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_39

>39.1|3315110|29|NZ_LN831776|CRISPRCasFinder
CATCTGCCCGAGGGTAGGGTACTCCGGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_39

CRISPR arrays

The CRISPR arrays of NZ_LN831776_39

>merge|NZ_LN831776|39|3315087-3315161|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTTCATCTGCCCGAGGGTAGGGTACTCCGGCAAATTAGTGTACCTTTTTCCACTT

>NZ_LN831776|39|41|3315087-3315161|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTT	CATCTGCCCGAGGGTAGGGTACTCCGGCA
AATTAGTGTACCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_046502935.1|3323201_3323468_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020434066.1|3310350_3310476_+|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|235546
NZ_LN831776.1|WP_020434069.1|3311924_3313520_+|GGDEF-domain-containing-protein	unknown	unknown	gnl|CDD|143635
NZ_LN831776.1|WP_020427573.1|3319208_3319754_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|168472
NZ_LN831776.1|WP_020434068.1|3310826_3311693_-|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|223669
NZ_LN831776.1|WP_046502938.1|3323813_3324362_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_LN831776.1|WP_020427571.1|3320308_3321100_-|hypothetical-protein	unknown	unknown	gnl|CDD|253605
NZ_LN831776.1|WP_020434062.1|3307203_3307941_+|GTP-pyrophosphokinase-family-protein	unknown	unknown	gnl|CDD|225232
NZ_LN831776.1|WP_157764282.1|3305743_3305896_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046502916.1|3313748_3314486_+|cupin-domain-containing-protein	unknown	unknown	gnl|CDD|380440
NZ_LN831776.1|WP_052741450.1|3321972_3322881_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213234
NZ_LN831776.1|WP_046502912.1|3307998_3309624_+|glycoside-hydrolase	unknown	unknown	gnl|CDD|376383
NZ_LN831776.1|WP_020434065.1|3309652_3310354_+|HAD-family-hydrolase	unknown	unknown	gnl|CDD|223943
NZ_LN831776.1|WP_020434061.1|3306027_3307059_+|HD-domain-containing-protein	unknown	unknown	gnl|CDD|225116
NZ_LN831776.1|WP_046502925.1|3319780_3320224_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831776.1|WP_020427575.1|3316980_3317577_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_LN831776.1|WP_020427574.1|3317686_3319096_+|NAD-dependent-malic-enzyme	unknown	unknown	gnl|CDD|223358
NZ_LN831776.1|WP_020434067.1|3310472_3310610_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046502929.1|3321108_3321939_-|hypothetical-protein	unknown	unknown	gnl|CDD|226953
NZ_LN831776.1|WP_046502922.1|3315867_3316860_-|acryloyl-CoA-reductase	unknown	unknown	gnl|CDD|176249

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020434066.1|3310350_3310476_+|SDR-family-NAD(P)-dependent-oxidoreductase	gnl|CDD|235546	PRK05653, fabG, 3-oxoacyl-ACP reductase FabG.	8.12105e-08
NZ_LN831776.1|WP_020434069.1|3311924_3313520_+|GGDEF-domain-containing-protein	gnl|CDD|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	2.0656e-65
NZ_LN831776.1|WP_020427573.1|3319208_3319754_+|AAA-family-ATPase	gnl|CDD|168472	PRK06217, PRK06217, hypothetical protein; Validated.	5.004e-79
NZ_LN831776.1|WP_020434068.1|3310826_3311693_-|alpha/beta-hydrolase	gnl|CDD|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	4.93132e-11
NZ_LN831776.1|WP_046502938.1|3323813_3324362_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.75481e-08
NZ_LN831776.1|WP_020427571.1|3320308_3321100_-|hypothetical-protein	gnl|CDD|253605	pfam06182, ABC2_membrane_6, ABC-2 family transporter protein. This family acts as the transmembrane domain (TMD) of ABC transporters. The family includes proteins responsible for the transport of herbicides.	5.89779e-28
NZ_LN831776.1|WP_020434062.1|3307203_3307941_+|GTP-pyrophosphokinase-family-protein	gnl|CDD|225232	COG2357, COG2357, PpGpp synthetase catalytic domain [General function prediction only].	6.65125e-88
NZ_LN831776.1|WP_020427574.1|3317686_3319096_+|NAD-dependent-malic-enzyme	gnl|CDD|223358	COG0281, SfcA, Malic enzyme [Energy production and conversion].	0
NZ_LN831776.1|WP_046502916.1|3313748_3314486_+|cupin-domain-containing-protein	gnl|CDD|380440	cd20306, cupin_OxDC-like, Oxalate decarboxylase (OxDC)-like cupin domain. This subfamily contains bacterial and eukaryotic cupin domains of proteins homologous to oxalate decarboxylase (OxDC; EC 4.1.1.2) such as MSMEG_2254, a putative OxDC from Mycobacterium smegmatis. OxDC is a manganese-dependent bicupin that catalyzes the conversion of oxalate to formate and carbon dioxide, utilizing dioxygen as a cofactor. It is evolutionarily related to oxalate oxidase (OxOx or germin; EC 1.2.3.4) which, in contrast, converts oxalate and dioxygen to carbon dioxide and hydrogen peroxide. OxDC is classified as a bicupin because it contains two cupin folds with each domain containing one manganese binding site, with four manganese binding residues (three histidines and one glutamate) conserved as well as a number of hydrophobic residues.	8.56122e-52
NZ_LN831776.1|WP_052741450.1|3321972_3322881_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|213234	cd03267, ABC_NatA_like, ATP-binding cassette domain of an uncharacterized transporter similar in sequence to NatA. NatA is the ATPase component of a bacterial ABC-type Na+ transport system called NatAB, which catalyzes ATP-dependent electrogenic Na+ extrusion without mechanically coupled to proton or K+ uptake. NatB possess six putative membrane spanning regions at its C-terminus. In B. subtilis, NatAB is inducible by agents such as ethanol and protonophores, which lower the proton-motive force across the membrane. The closest sequence similarity to NatA is exhibited by DrrA of the two-component daunorubicin- and doxorubicin-efflux system. Hence, the functional NatAB is presumably assembled with two copies of the single ATP-binding protein and the single integral membrane protein.	4.55328e-126
NZ_LN831776.1|WP_046502912.1|3307998_3309624_+|glycoside-hydrolase	gnl|CDD|376383	pfam00759, Glyco_hydro_9, Glycosyl hydrolase family 9.	3.40754e-58
NZ_LN831776.1|WP_020434065.1|3309652_3310354_+|HAD-family-hydrolase	gnl|CDD|223943	COG1011, COG1011, Predicted hydrolase (HAD superfamily) [General function prediction only].	6.28826e-23
NZ_LN831776.1|WP_020434061.1|3306027_3307059_+|HD-domain-containing-protein	gnl|CDD|225116	COG2206, COG2206, c-di-GMP phosphodiesterase class II (HD-GYP domain) [Signal transduction mechanisms].	6.90225e-44
NZ_LN831776.1|WP_046502925.1|3319780_3320224_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	7.4528e-13
NZ_LN831776.1|WP_020427575.1|3316980_3317577_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	5.26656e-14
NZ_LN831776.1|WP_046502929.1|3321108_3321939_-|hypothetical-protein	gnl|CDD|226953	COG4587, COG4587, ABC-type uncharacterized transport system, permease component [General function prediction only].	5.94444e-13
NZ_LN831776.1|WP_046502922.1|3315867_3316860_-|acryloyl-CoA-reductase	gnl|CDD|176249	cd08289, MDR_yhfp_like, Yhfp putative quinone oxidoreductases. yhfp putative quinone oxidoreductases (QOR). QOR catalyzes the conversion of a quinone + NAD(P)H to a hydroquinone + NAD(P)+. Quinones are cyclic diones derived from aromatic compounds. Membrane bound QOR actin the respiratory chains of bacteria and mitochondria, while soluble QOR acts to protect from toxic quinones (e.g. DT-diaphorase) or as a soluble eye-lens protein in some vertebrates (e.g. zeta-crystalin). QOR reduces quinones through a semi-quinone intermediate via a NAD(P)H-dependent single electron transfer. QOR is a member of the medium chain dehydrogenase/reductase family, but lacks the zinc-binding sites of the prototypical alcohol dehydrogenases of this group. NAD(P)(H)-dependent oxidoreductases are the major enzymes in the interconversion of alcohols and aldehydes, or ketones. Alcohol dehydrogenase in the liver converts ethanol and NAD+ to acetaldehyde and NADH, while in yeast and some other microorganisms ADH catalyzes the conversion acetaldehyde to ethanol in alcoholic fermentation. ADH is a member of the medium chain alcohol dehydrogenase family (MDR), which has a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The NAD(H)-binding region is comprised of 2 structurally similar halves, each of which contacts a mononucleotide. A GxGxxG motif after the first mononucleotide contact half allows the close contact of the coenzyme with the ADH backbone. The N-terminal catalytic domain has a distant homology to GroES. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit, a catalytic zinc at the active site, and a structural zinc in a lobe of the catalytic domain. NAD(H) binding occurs in the cleft between the catalytic and coenzyme-binding domains at the active site, and coenzyme binding induces a conformational closing of this cleft. Coenzyme binding typically precedes and contributes to substrate binding. In human ADH catalysis, the zinc ion helps coordinate the alcohol, followed by deprotonation of a histidine, the ribose of NAD, a serine, then the alcohol, which allows the transfer of a hydride to NAD+, creating NADH and a zinc-bound aldehyde or ketone. In yeast and some bacteria, the active site zinc binds an aldehyde, polarizing it, and leading to the reverse reaction.	4.47174e-177

Protein sequences

>NZ_LN831776.1|WP_046502916.1|3313748_3314486_+|cupin-domain-containing-protein
MDYKSPTTQFSFDVNSNTTFKKDDCNYINTLSVKELNTLENTSLLDIFLSRSNVVEPHYHQNSAELVYCISGAAVVSLINPFTNELLHFPITPGQVANVPQGWWHYEVATVDCTHLLAIFNAPVPEVILGSDLLTITPANVLAHTYCLNEAQVKDTLAPVKPGTFIGPPADCCEPGKTGGANAAHPNNMAPHPYPQSPQMLQPLGYQPSPMHGYYGQPYVQQYHGQPYVQPYPGLQPAVDPAGNV
>NZ_LN831776.1|WP_020434069.1|3311924_3313520_+|GGDEF-domain-containing-protein
MPRLGGAGQRPQKKLSLTLLLIGLVTLVVLLTSTILLTASYHSKKKSLIETTLNLNLANAERMSRTMDSLFRSMRSSMEYSADKLSKLHELSPGQVNDYLELMRKSSTYFNSILLVGADGIVRNTSPATLGMEGKPVMSPWAVEALRLKKPYLSEPYTALSTGRMIVFMSEPVYDPDKHYLGQLGGTIYLQDNNILNMIFGNTNDIDASGSYYYIVSSSGHLLFHPDKERINEDVSSSEVVQELMKGNSGQREAFNIRGVRMLAGYSSVQANGWGIVAVSPVSFIQEELWSQLRITLAYTLIPFVILLLLAVLLSHQLAQPFVMLADLMSRVGKGKAELPELKPHWNREADLLTKAVTIAWSNIQKHTDQLTQAAMTDLLTGLANRRSLELTMNQWIAAQFSFSVIVLDVDKFKFVNDTYGHLAGDEVLKQVADILKMSIRPGDVCCRYGGEEFVVLLPRTKASDAYTVAERIRKTLETSVVSQTVKVTSSQGIAHYPSHGSSLEELLQQADRAMYKAKGLGRNRTVIAEE
>NZ_LN831776.1|WP_020434068.1|3310826_3311693_-|alpha/beta-hydrolase
MKWIRNKTLPTLAIFMAFLVLLTALPFGGAAAEASALKSKPAPSGALTFVLVHGAWVDASFWDGIAAELRKMGHTVYTPEYAGHGADPDKNVTHEQETQSVVDFIKQKDLHHIILLAHSFGGTVIQKTAEQVPDRLKRLVFFDAFAPLDGQSAADQFPPPAAELFLGLSKASGNNTIMLPFDLFRDTFVNTATLEQAKLLYKKVIPEPAGPLFQKLDLKKFYSLKTPKSYLYLTEDIAMPELPSYGWHPVQSGHLGVYRFIEGTGDHMAAPHYAPKEIADKIVQASRD
>NZ_LN831776.1|WP_020434067.1|3310472_3310610_+|hypothetical-protein
MKHKHTGARVLPAVADPGNEQGCDRMVEQFPEALRADGGWVRSVF
>NZ_LN831776.1|WP_020434066.1|3310350_3310476_+|SDR-family-NAD(P)-dependent-oxidoreductase
MIVTGSAGAIGRAIAEVLLREGAEVLINGRSEDKVNAVVQD
>NZ_LN831776.1|WP_020434065.1|3309652_3310354_+|HAD-family-hydrolase
MNPYQVISLDMFQTLVNIEGRRNHIWRPILQQDFSEARALELGQALLTHYFAQAAAIRDAGSFCTSQEIYRRGFEKVFQEHLLSFDCHEAVDILFAEHRLSGLYADTVPFLQKISEAYQICIVSDTDTLMLPDFYKEYPIKLFTSEDYGSYKNDGRNRMFTEVIAYYGVQPEEILHIGDSASDVLGAARAGIRSCWINRTGSSWKHTVQPDYTVSNLEELYPILEPGAPAEPA
>NZ_LN831776.1|WP_046502912.1|3307998_3309624_+|glycoside-hydrolase
MSTPDLRSITVNQIGYSTEGVKIAVINGEGQNFRVIHEETGTVVYAGKSGAAVLDKPSGAKAQTADFSEVRTAGRYYVEGEDGAVSASFVIANKPYQELQQGLLKAFYYFRCGVELTGEYAGPWAHGPCHTAEGIVHGQPEKRLDCCGGWHDAGDYGKYSGPGAKAIADLLLAYELYPAAFAAAVPLPESDGRTPDVLLECRVELDWLLKMQEAGTGGVYHKLTTLSFPGLDVMPEDDTAELYISPVSAAATGDFAGVMAMAARVYEPYDQAYARRCLAAAQAAWTWLEQHPGVSGFTNPPGITTGEYGDGNDQDERFWAAAELYRATGREVYHEAAQALAKQPFPKYSLGWADMGGYGTLAYLLSGESAAQTALYASLKQGLLAEADRLVRLSRDDGYRISLREEDYIWGSNMLVMNNAMLLLAAEHFSGNIAYADCALDHLHYLMGRNVLDISYVTGFGDRPVMHPHHRPSVGDGVADPVPGMVSGGPDRGLHDEYVALHLQGKPAAQCFADHDLSYSTNEVTIYWNSPAVFVTARFNV
>NZ_LN831776.1|WP_020434062.1|3307203_3307941_+|GTP-pyrophosphokinase-family-protein
MSTQDQIEKFKQLKYELTRFMMIYKFALEEMETKIEILKQEFQMLHDYSPIEHTKSRIKSPESIMNKMLRKNNELSLPAIRATIKDIAGLRITCSFISDIYQVSAMLQKQDDLKVLGVKDYIKHPKPNGYQSLHLLVEVPVFLSDCQEHVCVEVQIRTIAMDFWASLEHKIFYKYSQSVPEHLTRELKNAADKAYELDLQMERLHREIKEIKDAQGDDTDVELRRIMINNQQFNLPANFIKLLGE
>NZ_LN831776.1|WP_020434061.1|3306027_3307059_+|HD-domain-containing-protein
MKVHVTDLKHGDCLLTDTFNSVGLHVLPKRTVVQREEITILLRHKIEYVDIEPRTASHAEDSGLGHSLNDNFDHAIQNYESIFLEALAQGTFTQSMVDDTLQPLLETLDTQKDVVSLLLLLERDDIDTYHHSLQVGLLSYYIAAWMGHSKEERYEISRAGYLHDIGKSQVPLSILNKAGILTPAEEEELKRHTTFGYEIIRGSKMDEKTALVALQHHEFEDGTGYPNQILKSGIHPYTEIVTVANIYMGLTTSRLNQPKQGLVAVLRKVHEMGFGKLNGTVVQALTGHLLPGFVGKNVQLSNGEIGTIVMNNPLDMFRPLVKVDNVFKDLSRERSLSVEEIIM
>NZ_LN831776.1|WP_157764282.1|3305743_3305896_+|hypothetical-protein
MGIKPIGNRIVPIRLSFRFIDDREQAMKQLTRWAEENRVKLTYKRFVKWM
>NZ_LN831776.1|WP_046502922.1|3315867_3316860_-|acryloyl-CoA-reductase
MTETFKALVVDKGETFSVAVQPLSLEKLPAGEVLIRVAYSSVNYKDGLASIPNGNIVRNYPFIPGIDLSGTVVSSADPRFHEGQAVIATGYGIGVSHYGGFSEYARIPAGWVMPLPAGLSLREAMIYGTAGFTAAMSIQALEAHGAAPDKGKVLVTGATGGVGGTAVAMLAKKGYQVTASTGQADADSYLKTLGAAEIISREEVSGGSGKPLDKQLWQAAVDSVGGAPLAALLSKIAYGGSVAASGLTAGTAVPATVLPFILRGVSLLGIDTVACPIEQRIQIWERMASDLKPERLDALVDREVTLTELPAALEDILTSNTRGRVLVRLS
>NZ_LN831776.1|WP_020427575.1|3316980_3317577_+|TetR/AcrR-family-transcriptional-regulator
MVRYKKSEEKRKQILFAAFQALSELGYDSVTLQTIADHAEVSKGVVHYYFDNKEAVLVELLEWLTAKISAKEQAAVQEQQTAAGKLKAYIDSAFPGPAKNRSFYRVYLDFLARASRIPVYREINQRFYDNCARISTEVLTLGQKEGIFAKELAPDTTAPVIRAIIDGCLIQWLMKDDDELHAAYKEMCYEAVMKVLRV
>NZ_LN831776.1|WP_020427574.1|3317686_3319096_+|NAD-dependent-malic-enzyme
MSIATTMIIRLEIRKSVATFGDVASRLAAVGGDIVAIDVIRAGKDVTTRDITVNVQDAANEEIITVLKDMPGIKVINISDRTFLAHIGGKIEITPKIPIKNREDLSLVYTPGVARVCMAIAEDPGRAYSLTMKRNTVAVVTDGTAVLGLGDIGPEAAMPVMEGKAMLFKQLADIDAFPLCLGTKDPEEIIRVVKAVTAGLGGINLEDISSPRCFEIERRLSAELDIPVFHDDQHGTAVVALAGLLNALKVVGKRLEDCRIVVVGIGAAGVSICRLLLAAGARKVYAVDRAGILHKGQTYDNAEWSWLAEATNPEGLTGGLTEAMQGADVFIGVSSGGILSEDHLKSMAEDNIVFAMANPTPEIEPELAESYARVVATGRSDYPNQINNVLCFPGIFRGALDCRAKVVNLEMKLAAAQAIASVVHPDELNEQYIIPSIFNEKVVEGVREAVIRAAIATGMARRLPPDISE
>NZ_LN831776.1|WP_020427573.1|3319208_3319754_+|AAA-family-ATPase
MYSRIHIMGASGAGTSTLGRALAGHLPHVHLDSDDYFWEHKYTQQTELTERLRTIQRDLDQQEPYILSGAVCGWGDGLRPRFDLVVFLWIPPEIRLERLRMRENERYGADSLPGGSMYQEVQTFMEWAALYDTAGPEVRSRVLHEEWMSHLQCPVLRLEEDMTVAARVEAVLREYAAKITQ
>NZ_LN831776.1|WP_046502925.1|3319780_3320224_+|GNAT-family-N-acetyltransferase
MVTIKEIEFESLGALNRLYDELIGGPTDPQKLEAAFQSVKADSRYILLGAFVDGELLGSMMGIICQDLVGDCRPFMVIENVVVSSRARRQGLGKKLIAALEAIAHERDCYYIMFVSGEKRKEAHIFYEAMGYREEKVEGYRKHLSSH
>NZ_LN831776.1|WP_020427571.1|3320308_3321100_-|hypothetical-protein
MIAESKIYFKYLRMHLLSGMEYKGWWLMLIQVLVVVISDPIATVLLFSRFGNIGEWTVAHIILVYALAVASFGLAESLCRGFDYFPWQMLRSGDFDRLLLRPRSLFVQVAASRFHLHRLVRPVTGICAMGWALSELGVSLTPGKLLVLAMALAGGCVMYCGVFVLTSGLAFFTIKGLDWIYLLTNASYQITRCPEPYMPRALKSMFSFVLPMLFISFYPAATVCGWDYPQWLGYLALPAGAAFLGFSLLVWRFGVRHYKSTGS
>NZ_LN831776.1|WP_046502929.1|3321108_3321939_-|hypothetical-protein
MNFRSTFKACISLFRIRMAEGLQYRASAISGVFVSVFWGLLECVLFTVFYTYSDNGAWNNNGLALPQTISYVWLAQGLFVLQTMSIDSEIMGKINNGDVGVELCRPLNLYTHWFVKSSAGKLGTSWLRSLATILTGLLMPAGYALGAPASALGFACFLLSVVMAFVLCSSFAMFVTAIRLNITWGDGPTYMLLLFSGILSGTYLPLRLWPDFMQTFLYLQPFGGFADIPVQLYVGSLMPSAALPAIGLQFFWSAVFIAAGRTIMNHKLRSIIVQGG
>NZ_LN831776.1|WP_052741450.1|3321972_3322881_-|ATP-binding-cassette-domain-containing-protein
MLLGWNHGRENAILSQRPVNVMIFCTKEVHQMQIVLKDICKTFRVYKRPEGKWGLLRGAFMRNVTHVEALAGIGFEIAEGELVGYIGPNGAGKSTTVKVMSGILTPDSGECTIMGKVPWKNRVEHVSKIGVVFGQRSQLWWDVPVADSFDVLKDIYAIPAGDYKTRLTELTATLGVEALLKTPVRQLSLGQRMRCELVAALLHRPKILFLDEPTIGLDAVSKLALRTFLKEENRNYGVTMVLTTHDMDDIEALCERVMVIGHGQLLYDGRLGGLQEKYAPEVITKVNTDAMIAAMYNDLSLV
>NZ_LN831776.1|WP_046502935.1|3323201_3323468_+|hypothetical-protein
MRGRNTFDFGADRLCGRMRGKNTFDFGVDRPYGEMRGKNTFDFGADRLCGRMRGKNTFDFGVDRPYGEMRGKNTFDFGVDYPIWRNER
>NZ_LN831776.1|WP_046502938.1|3323813_3324362_-|TetR/AcrR-family-transcriptional-regulator
MKKQPETTEKTRQMFIDVFCELYSQKPIEKISIQELANKSGYNRSTFYQYFSDIYELLDFVENNLLSYIKEELANKELSMHTVQNALHCLDKREYLSILSALLGDYGSTRFLERLKREITLDSLEFNSPQNHSITPYLIEFYLSTSLSLFRLWLRREKDLSSEEFFRLVDNLYTKGIAPYSK

Crispr_ID: NZ_LN831776_40

• CRISPR_ID: NZ_LN831776_40
• CRISPR_location: 3575971-3576251
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 5 spacers

Consensus repeat of NZ_LN831776_40

Consensus_repeat	Method
AATGAGAGGTAAAANTNCCNTTGANT	CRT

spacers of NZ_LN831776_40

>40.1|3575997|25|NZ_LN831776|CRT
TTGGAGCAAACGGGTAAAAGGGAGG
>40.2|3576048|25|NZ_LN831776|CRT
TGTCCAAAAGCGGGCAGCTGAAGGA
>40.3|3576099|25|NZ_LN831776|CRT
TTGAAGCAAACGGGTAAAAGGGGGG
>40.4|3576150|25|NZ_LN831776|CRT
TGTCCAAAAGTGGGCTACGGTGTGA
>40.5|3576201|25|NZ_LN831776|CRT
CTGGCGCAAGCGGGCTGATGAGCGG

CRISPR arrays and Neighbor proteins around NZ_LN831776_40

CRISPR arrays

The CRISPR arrays of NZ_LN831776_40

>merge|NZ_LN831776|40|3575971-3576251|CRT
AATGAGAGGTAAAAATGCCTTTGAATTTGGAGCAAACGGGTAAAAGGGAGGAATGAGAGGTAAAAGTACCCTTGATTTGTCCAAAAGCGGGCAGCTGAAGGAAATGAGAGGTAAAAATGCCTTTGAATTTGAAGCAAACGGGTAAAAGGGGGGAATGAGAGGTAAAAGTACCCTTGATTTGTCCAAAAGTGGGCTACGGTGTGAATTAAGAGGTAAAAGTGCTTTTGAATCTGGCGCAAGCGGGCTGATGAGCGGAATGAGAGGTAAAAGTGCCTTTTGAC

>NZ_LN831776|40|5|3575971-3576251|CRT
AATGAGAGGTAAAAATGCCTTTGAAT	TTGGAGCAAACGGGTAAAAGGGAGG
AATGAGAGGTAAAAGTACCCTTGATT	TGTCCAAAAGCGGGCAGCTGAAGGA
AATGAGAGGTAAAAATGCCTTTGAAT	TTGAAGCAAACGGGTAAAAGGGGGG
AATGAGAGGTAAAAGTACCCTTGATT	TGTCCAAAAGTGGGCTACGGTGTGA
ATTAAGAGGTAAAAGTGCTTTTGAAT	CTGGCGCAAGCGGGCTGATGAGCGG
AATGAGAGGTAAAAGTGCCTTTTGAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020431823.1|3573275_3573752_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831776.1|WP_167345698.1|3581955_3582630_-|tetratricopeptide-repeat-protein	unknown	unknown	gnl|CDD|379646
NZ_LN831776.1|WP_020431845.1|3584404_3584617_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020431821.1|3572657_3573218_+|hypothetical-protein	unknown	unknown	gnl|CDD|394878
NZ_LN831776.1|WP_144412152.1|3585444_3586536_+|fibronectin-type-III-domain-containing-protein	unknown	unknown	gnl|CDD|236940
NZ_LN831776.1|WP_167345622.1|3574685_3575213_+|VanZ-family-protein	unknown	unknown	gnl|CDD|377417
NZ_LN831776.1|WP_020431841.1|3582924_3583926_+|aldo/keto-reductase	unknown	unknown	gnl|CDD|381319
NZ_LN831776.1|WP_020431819.1|3571326_3571974_-|fructose-6-phosphate-aldolase	unknown	unknown	gnl|CDD|234947
NZ_LN831776.1|WP_020431843.1|3584132_3584291_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_167345697.1|3574036_3574717_+|ribose-5-phosphate-isomerase-RpiA	unknown	unknown	gnl|CDD|234816
NZ_LN831776.1|WP_020431817.1|3570705_3571149_-|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_LN831776.1|WP_020431831.1|3576444_3576897_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_LN831776.1|WP_020431824.1|3573760_3573958_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020434002.1|3586887_3588249_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_LN831776.1|WP_020431820.1|3572206_3572674_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046503185.1|3580242_3580776_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|213752
NZ_LN831776.1|WP_046503189.1|3580772_3581882_+|DUF4179-domain-containing-protein	unknown	unknown	gnl|CDD|379369
NZ_LN831776.1|WP_020431828.1|3575275_3575716_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379228
NZ_LN831776.1|WP_046503181.1|3576893_3580052_+|MMPL-family-transporter	unknown	unknown	gnl|CDD|225272
NZ_LN831776.1|WP_167345623.1|3575726_3575939_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020431823.1|3573275_3573752_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	1.10363e-20
NZ_LN831776.1|WP_167345698.1|3581955_3582630_-|tetratricopeptide-repeat-protein	gnl|CDD|379646	pfam14559, TPR_19, Tetratricopeptide repeat.	3.08085e-05
NZ_LN831776.1|WP_020431821.1|3572657_3573218_+|hypothetical-protein	gnl|CDD|394878	cd02908, Macro_OAADPr_deacetylase, macrodomain, O-acetyl-ADP-ribose (OAADPr) family. Macrodomains are found in a variety of proteins with diverse cellular functions, as a stand-alone domain or in combination with other domains like in histone macroH2A and some PARPs (poly ADP-ribose polymerases). Macrodomains can recognize ADP-ribose (ADPr) in both its free and protein-linked forms, in related ligands, such as O-acyl-ADP-ribose (OAADPr), and even in ligands unrelated to ADPr. This family includes eukaryotic macrodomain proteins such as human MacroD1 and MacroD2, and bacterial proteins such as Escherichia coli YmdB; these have been shown to be O-acetyl-ADP-ribose (OAADPr) deacetylases that efficiently catalyze the hydrolysis of OAADPr to produce ADP-ribose and free acetate. OAADPr is a sirtuin reaction product generated from the NAD+-dependent protein deacetylation reactions and has been implicated as a signaling molecule. By acting on mono-ADP-ribosylated substrates, OAADPr deacteylases may reverse cellular ADP-ribosylation.	4.34991e-69
NZ_LN831776.1|WP_144412152.1|3585444_3586536_+|fibronectin-type-III-domain-containing-protein	gnl|CDD|236940	PRK11633, PRK11633, cell division protein DedD; Provisional.	9.53104e-09
NZ_LN831776.1|WP_046503185.1|3580242_3580776_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|213752	TIGR02954, RNA_polymerase_ECF-type_sigma_factor, RNA polymerase sigma-70 factor, TIGR02954 family. This group of sigma factors are members of the sigma-70 family (TIGR02937). They and appear by homology, tree building, bidirectional best hits and one-to-a-genome distribution, to represent a conserved family. This family is found in certain Bacillus and Clostridium species.	6.93861e-37
NZ_LN831776.1|WP_020431819.1|3571326_3571974_-|fructose-6-phosphate-aldolase	gnl|CDD|234947	PRK01362, PRK01362, fructose-6-phosphate aldolase.	9.58789e-142
NZ_LN831776.1|WP_020434002.1|3586887_3588249_+|extracellular-solute-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	3.37829e-42
NZ_LN831776.1|WP_046503189.1|3580772_3581882_+|DUF4179-domain-containing-protein	gnl|CDD|379369	pfam13786, DUF4179, Domain of unknown function (DUF4179).	5.65257e-13
NZ_LN831776.1|WP_020431817.1|3570705_3571149_-|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	1.49011e-17
NZ_LN831776.1|WP_020431831.1|3576444_3576897_+|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	3.03391e-24
NZ_LN831776.1|WP_020431841.1|3582924_3583926_+|aldo/keto-reductase	gnl|CDD|381319	cd19093, AKR_AtPLR-like, Arabidopsis thaliana pyridoxal reductase (PLR) and similar proteins. Arabidopsis thaliana PLR (EC 1.1.1.65) is the prototype of this family. It catalyzes the reduction of pyridoxal (PL) with NADPH and oxidation of pyridoxine (PN) with NADP(+), and is involved in the PLP salvage pathway.	1.46965e-97
NZ_LN831776.1|WP_046503181.1|3576893_3580052_+|MMPL-family-transporter	gnl|CDD|225272	COG2409, COG2409, Predicted drug exporters of the RND superfamily [General function prediction only].	1.33505e-90
NZ_LN831776.1|WP_167345697.1|3574036_3574717_+|ribose-5-phosphate-isomerase-RpiA	gnl|CDD|234816	PRK00702, PRK00702, ribose-5-phosphate isomerase RpiA.	1.15629e-113
NZ_LN831776.1|WP_020431828.1|3575275_3575716_+|GNAT-family-N-acetyltransferase	gnl|CDD|379228	pfam13508, Acetyltransf_7, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	8.17885e-11
NZ_LN831776.1|WP_167345622.1|3574685_3575213_+|VanZ-family-protein	gnl|CDD|377417	pfam04892, VanZ, VanZ like family. This family contains several examples of the VanZ protein, but also contains examples of phosphotransbutyrylases.	2.09955e-21

Protein sequences

>NZ_LN831776.1|WP_167345623.1|3575726_3575939_+|hypothetical-protein
MNVLRAQRQHQVQAISHCYNAGWLFLSDSTKGRMQTGNNGRNAFVEALKAGMFLLMETIQCKKKRILKAG
>NZ_LN831776.1|WP_020431828.1|3575275_3575716_+|GNAT-family-N-acetyltransferase
MLVDLKQRTDTDEVKELLAYAVIDEPDALWRTSVEYGSKAALQLFGWEEEGLLIGLVGFEETEDGSLEIRHIAVLPENRGKGYARGIILELLAARNPRYLLAETEDEIAADFYRNLGFMVYSLGESPAGIEMFRCVYEVEEDEDED
>NZ_LN831776.1|WP_167345622.1|3574685_3575213_+|VanZ-family-protein
MKLLSVNTASNRQKQGNPRPRSGKRHTPAQPGRLGRAMLLILLIAYSAALVYWMFIGFGRSVHTDGPFRYNLEPLRTIKLYFDLDNGVSFPRRLINLLGNVIVFVPFGVLLPLLRKSLRSVLALLFVSALGILLLETMQMLLRVGSFDIDDLLLNLAGVLCGYILLWSVFLKGKR
>NZ_LN831776.1|WP_167345697.1|3574036_3574717_+|ribose-5-phosphate-isomerase-RpiA
MNVKQLAAEKAVEYVVDGMKVGLGTGSTAYWAIRKLGERVQEGLKITAVATSVASEEQARELGIPLVSFGDIDGLDLTIDGADELNHDLELIKGGGGALLREKIVARGSKRMIVVADESKAVGMLGQFPLPVEIVPFAWEWTVADLAKLGCTVELRRSGDGLYKTDNGNYIADCRFGTIASASELAASLQNITGVVEHGLFIGIAALAIIGKQDGSIEIIEREHGE
>NZ_LN831776.1|WP_020431824.1|3573760_3573958_-|hypothetical-protein
MRTEQQIQSKINELTLQKRSLESRLAPLPGGSPQREPLNAQLTRLEDMLLMLEWVLDAPAGKYHA
>NZ_LN831776.1|WP_020431823.1|3573275_3573752_+|GNAT-family-N-acetyltransferase
MISKSEVNFVVVEPENRELRALIDRLDDELKARYPHETIYVVDFSDPKVREMTFVVAYAGDKPVGCGGLRPLDPDSSVMELKRFFVDPDTRKQGIANRMLLDLEQKARAAGCREIRLETGIKQPEAIALYEKHGYRPIDLFGPYIGDPDSLCYGKSLS
>NZ_LN831776.1|WP_020431821.1|3572657_3573218_+|hypothetical-protein
MPIFINQVAISACQGDITSWQGDMIVNASNSGLFGGGGVDGAIHRAGGPQIAEECAAIRRKQGGILPGEAAVTCAGKLPLLGIIHTVGPIWKGGGAGEIATLARCYLNSLDAACTQGARSIAFPNISTGVYNFPKALACQTALKTVVDYVKERGPGGHPLERIEFICFEKDNADLYEETLKRYSDI
>NZ_LN831776.1|WP_020431820.1|3572206_3572674_+|hypothetical-protein
MFMVFAGVIVFLLFAAGVMAYQNSRLIAQQEASDSAGRISSLMYSVYYQAFSYNEERPEAVPLFQFTVRARTEGQPASGEVDKTIALCRVPAGSGEMALSDAQNWMLGSIRQSALRGESIFPASFQDKAASKGEQELILRLETAVKEETGHANLH
>NZ_LN831776.1|WP_020431819.1|3571326_3571974_-|fructose-6-phosphate-aldolase
MKFFLDTGNIEEIKRITRLGLVDGVTTNPSLIAKEGRLFKDVIKEIVAIVPGPVSAEVIGLKAEEMLKEAYEIAEWAPNVVIKLPMTEDGLEACYELTKKGIKTNVTLIFSAAQGLMAAKAGATYISPFVGRLDDIGVDGMKLISDLKTILTNYGLQSEIIAASIRNIAHVEQAAIAGAHIATIPGSLLPSLWKHPLTDNGIERFLKDWEKVPQA
>NZ_LN831776.1|WP_020431817.1|3570705_3571149_-|MarR-family-transcriptional-regulator
MPLTSPQEFLGFLLGSTHRRISNAFARVLKPYDITPEQWSILLMICDREGINQKEVAAAAAKDQPTTARIVELLQKKGFIHKTMSPTDRRAFQLYATETGKSLIKRTVSLEQQTIAAAVNGLRPEQIEDLRSMLELIYHNTGNTHQE
>NZ_LN831776.1|WP_020431831.1|3576444_3576897_+|MarR-family-transcriptional-regulator
MKGEPQHWIDRYIDAYMGVTRQINAQIKDNMAECLTNDQFLIMRLINSQEPCTSTFLAEAVAVGKSSITAIINRLAEAGFIERTRDENDRRQVYLSLTEKGKSTYHAAEKQVQEVISPYFSHFEEQDIEKFITMFEKLALLMQETGGRNN
>NZ_LN831776.1|WP_046503181.1|3576893_3580052_+|MMPL-family-transporter
MKTVLKARWAIIAVWLAAAVVLFMTAPGMSDLVREKGQISVPDGYTSTRAAEIMKEVADAKGGETLHQVALVFNKPDGLAAEDTESIKQGVEKLAAEKEALKIDSITDPFSQAELKDTLIAKDGKTIMVALMVNGGEEAVKQLPDQVDKLLSGVSADHYLTSEGLITEDTIVSSEAGLKKSEYITVIFILLILFVVFRSFVAPFVPLLTVGLSYIVSQSIVAFLVDRFDFPLSTFTQIFMVAVMFGIGTDYCILLISRFKEELATAEDTRSAIISTYRKAGGTVFYSGLAVFVGFLAIGLSKFMLYRSAVAVAVGIAVMLLALVTVVPFFMAVLGKKLFWPSSSKLEHSESGIWGAAGSFSLKRPWAALLIVAVVVVPFLLTYSGKLSFNSMDEIGPGYASVKGFNIISDSFGPGESMPGKIVIKNDDRMDTSEYMGLAEKISRELEKVDGVKAVRSMSRPTGEQINDFLIPTQVAALTDGLSQSNEGLTKIQSGLEEASKQLKGNEPKLNEAVSGSAKLTEGTAELKKGIDALGDGLSRIERGIKSGSSGAGEIKAGLAQAAASAKQLADANAALLAGYQKIGAGLTALNGGLGQLQTQLQGVASALAGLDASFTGLENAHPDLLQDVNYQTIKGTVTQSGTGAAKLAGGLGQISGQLKGAAAGLNEANAGYAKAAAGQTALAQGLDKLVAGIGQLQSGLNQAAAGQGQIVDKIPSISSGLNQLQGGQQQLADGFGQLTGQIGKLTDGLSDSADGLKQITGGLNSAQDYLKQIQDAKDDELSGFLVPEEALKEGGIQQVFDNYLSSDRKVMTLDVVYAANPYSAKAIDSMGDIQAAVDRAVKGTKLENAETAISGVSSTYSDLQKISNEDYTRTVVLMLGGIFIILVVLLRSIIMPLYLIVSLLITYFTALGVTEAIFVHVLDYSGITWTTPFFSFVMLIALGVDYSIFLMDRFNENKTWDVREAILHAMRNMGTVILSAVVILGGTFASMYPSGVLSMMQIATVVLSGLALYALVFLPFFVPVMVRMFGRANWWPFSGSASADTPKTLDM
>NZ_LN831776.1|WP_046503185.1|3580242_3580776_+|sigma-70-family-RNA-polymerase-sigma-factor
MDNRLEKRVRRAQKGDNEAFIELIQEMELQMYQMAKSIVRKDEDCADAMQESTLKAFKAISTLKQPEFFRTWLFRILINECNMILRRRVQTVTIAETPVTPDERLSMAERMDLRTAVHQLEEIPRTLVILHYYQGFPLQHIADLLEMSEGAVKTRLHRARKTLYEWLADPVEREMNG
>NZ_LN831776.1|WP_046503189.1|3580772_3581882_+|DUF4179-domain-containing-protein
MNPKQLDQELDGLRGDKAEEVPELVRSRMNSVYQELKGSGEKVTPGRRRRSWWQRLLITAACAAVAVLLTIGLGFISPAMAETLKQLPFMKSVFQLAGDSGLKQASITGVTSGVQQSVTHGDLTLSISELMYDGSRLSLVLTKKESDGGNPSFYEWWNTRDMQLGPANNIDFYINGELANTAWGMAPGGTASPESVIVTALESPNLHVPEAFNFKMVVFIPDIGQTFSFELPVKKKTLESIVLRPEAAKTFDHINLHIKRLEISQTTIRLITEVKGAPGQDIKALQEAIPDKYKIYGSLNLLFDLQNDQGQTATMIGGNGNGQGNALSSSSSYEPFAAMPKSVVIKPYIWTQDSSKLYIPELEMTIPVQ
>NZ_LN831776.1|WP_167345698.1|3581955_3582630_-|tetratricopeptide-repeat-protein
MMLKFFGFLLLYRLVGNPFLALIILLVILYFLDRRYVGILPSFTKPFRRSRQISKLRTTISLNPNDVSAKFDLARLLIERKRYSESKELLEQIADRYEQSAEYWVELGYANLKLGHLPEGEAQMLQGLEINRKAQYGQPYLRLAEVFRNIDHNKALQYVTQFQEIQSSSSEAYYLAGSMYKALGRKEDAKRAFNESTAVYRSLPKYKKRQERGWALRSYFAKMR
>NZ_LN831776.1|WP_020431841.1|3582924_3583926_+|aldo/keto-reductase
MESAMAAAGLRPLGQSTLSVSPLGLGCWQFSRGKGIVGKYWGNLEDADILEIVRVSLEGGMNWVDTAEIYGGGKSEEALAYVLDQLKREGRPYATPLIATKWWPLFRTANSITSTIDERIRCLGGRDIDLYQIHQPFSLSTIASEMKAMAGLVQAGKIRNVGVSNYSAKQMTEAHHLLRQYGLNLVSNQVKYNLLDRKIDRNGTMEAAKALGISIIAYSPLQQGILTGRFHKDPAQIRAVSRVRRIQSGLDDKSLARSKPLIDSLTVLADKYGATPGQIALNWLIHYNGETVVAIPGASKVRHAQENIGALGFRLEKDELEHLNDVSWSALKS
>NZ_LN831776.1|WP_020431843.1|3584132_3584291_+|hypothetical-protein
MSMTVHNLMAFNHQYFRPQPVTDPKPQRSDDTTLSFQEILNEKLKAHSGMKK
>NZ_LN831776.1|WP_020431845.1|3584404_3584617_-|hypothetical-protein
MPINRPLLTDSDFQEAVDRKLPVRVFEDDHLVNSGATVIRFTDSDVVIQSRVSDLAYYSRSTCQFYEVRP
>NZ_LN831776.1|WP_144412152.1|3585444_3586536_+|fibronectin-type-III-domain-containing-protein
MQGVAVPEGSTVSATGKINAGRTTNLAIDGDINTYWNSAGFSDTLVILFPKEIDLNFIQLASVATPSNASVSYTISGYQSGTWIKISDTITKKINNVNKDYAVLEPINVKMGNYSGIKIEASSNKSTWIAIAEVTLGTEFIQDLIATAGDSQVSLNWSAVEIADSYTVKYGTESGEYTQSAIATKDEYGNFVIPGLTNGTTYYFVVSAMVNGVATDYSNEASATPIAPEPTPTATPTVTPEPTIEPTPTATPSPKPTATPSPTPSPTPSPTPSPTPSPTPEQPTGDRAILVVTMNTGLEKEFDLSMDEVNAFIAWYENKQGGTGTASYAINKHDNNKGPFTSRKDYIIFDKILTFSVDEYSAK
>NZ_LN831776.1|WP_020434002.1|3586887_3588249_+|extracellular-solute-binding-protein
MRKAKHLAVSLAAVLLVGSLAGCGGSNNAGKDNTTKENSGNNAASTNAPATDKAADPAEKIELSFWTLGNVNYEELANAYTKEHPNVTIKIQNTGDQTAHHNNLTTALSAGSGAPDIFQLEIGFMERFLSAQDKFYNLNDYGAKDIQANYLDWKWKQASSVDGSFQLGLPTDIGPTVVYYRTDLAKKAGLPEDPDGFGAAIDTWDKFATVAKAYKDKIGKPFVDLTDLTYNALRDQSNDEIYFSKADGKFIGDTNPQVKKAYDFTVKGIQEGWISNFMLWSPEWGQGMNDGSFAVIMGPAWMAGNIKSNAPDTSGKWKIAQLPEGAGNWGGSFITLPKEGKHPKEAYDFIQWLVNKDNQLESFKTKGLMPSIPALYEDPAFKDFKDDFFGGQQTAVEFGKSANRVKPVYYGPLHDQTDTFFKNALKNVLEKKADPAKEWDEAVKQAKTLAERG

Crispr_ID: NZ_LN831776_41

• CRISPR_ID: NZ_LN831776_41
• CRISPR_location: 3669445-3669519
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_41

Consensus_repeat	Method
AATTAGTGTCCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_41

>41.1|3669468|29|NZ_LN831776|CRISPRCasFinder
CATCTGCCCGAGGATAGGGTACTCCGGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_41

CRISPR arrays

The CRISPR arrays of NZ_LN831776_41

>merge|NZ_LN831776|41|3669445-3669519|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTTCATCTGCCCGAGGATAGGGTACTCCGGCAAATTAGTGACCCTTTTTCCACTT

>NZ_LN831776|41|42|3669445-3669519|CRISPRCasFinder
AATTAGTGTCCCTTTTTCCACTT	CATCTGCCCGAGGATAGGGTACTCCGGCA
AATTAGTGACCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_052741461.1|3664865_3665276_+|hypothetical-protein	unknown	unknown	gnl|CDD|237855
NZ_LN831776.1|WP_020433247.1|3673854_3674754_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_046503294.1|3675665_3676658_+|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_LN831776.1|WP_020433258.1|3679300_3682687_+|hypothetical-protein	unknown	unknown	gnl|CDD|225990
NZ_LN831776.1|WP_046503272.1|3661484_3662948_-|serine-hydrolase	unknown	unknown	gnl|CDD|224594
NZ_LN831776.1|WP_039786833.1|3666140_3667484_+|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_LN831776.1|WP_020427274.1|3660643_3661420_+|exodeoxyribonuclease-III	unknown	unknown	gnl|CDD|197321
NZ_LN831776.1|WP_020433255.1|3676803_3678969_+|beta-glucosidase-BglX	unknown	unknown	gnl|CDD|185053
NZ_LN831776.1|WP_020427275.1|3660187_3660475_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020433259.1|3683117_3683369_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046503289.1|3672477_3673722_+|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270450
NZ_LN831776.1|WP_020433249.1|3674797_3675622_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_039786834.1|3665426_3666140_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_LN831776.1|WP_020427276.1|3658760_3659879_+|citrate-synthase/methylcitrate-synthase	unknown	unknown	gnl|CDD|99862
NZ_LN831776.1|WP_046503281.1|3670287_3671424_+|DUF4179-domain-containing-protein	unknown	unknown	gnl|CDD|379369
NZ_LN831776.1|WP_020428465.1|3669761_3670298_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|213752
NZ_LN831776.1|WP_046503278.1|3664400_3664748_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427266.1|3667620_3668853_+|aminopeptidase	unknown	unknown	gnl|CDD|376723
NZ_LN831776.1|WP_046503285.1|3671486_3672041_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|227915
NZ_LN831776.1|WP_046503275.1|3663048_3664182_-|VanZ-family-protein	unknown	unknown	gnl|CDD|377417

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_052741461.1|3664865_3665276_+|hypothetical-protein	gnl|CDD|237855	PRK14900, valS, valyl-tRNA synthetase; Provisional.	0.000230158
NZ_LN831776.1|WP_020433247.1|3673854_3674754_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	5.61527e-81
NZ_LN831776.1|WP_046503294.1|3675665_3676658_+|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	2.56268e-112
NZ_LN831776.1|WP_046503272.1|3661484_3662948_-|serine-hydrolase	gnl|CDD|224594	COG1680, AmpC, Beta-lactamase class C and other penicillin binding proteins [Defense mechanisms].	3.99486e-32
NZ_LN831776.1|WP_039786833.1|3666140_3667484_+|HAMP-domain-containing-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	2.18896e-47
NZ_LN831776.1|WP_020427274.1|3660643_3661420_+|exodeoxyribonuclease-III	gnl|CDD|197321	cd09087, Ape1-like_AP-endo, Human Ape1-like subfamily of the ExoIII family apurinic/apyrimidinic (AP) endonucleases. This subfamily includes human Ape1 (also known as Apex, Hap1, or Ref-1) and related proteins. These are Escherichia coli exonuclease III (ExoIII)-like AP endonucleases and they belong to the large EEP (exonuclease/endonuclease/phosphatase) superfamily that contains functionally diverse enzymes that share a common catalytic mechanism of cleaving phosphodiester bonds. AP endonucleases participate in the DNA base excision repair (BER) pathway. AP sites are one of the most common lesions in cellular DNA. During BER, the damaged DNA is first recognized by DNA glycosylase. AP endonucleases then catalyze the hydrolytic cleavage of the phosphodiester bond 5' to the AP site, and this is followed by the coordinated actions of DNA polymerase, deoxyribose phosphatase, and DNA ligase. If left unrepaired, AP sites block DNA replication, and have both mutagenic and cytotoxic effects. AP endonucleases can carry out a variety of excision and incision reactions on DNA, including 3'-5' exonuclease, 3'-deoxyribose phosphodiesterase, 3'-phosphatase, and occasionally, nonspecific DNase activities. Different AP endonuclease enzymes catalyze the different reactions with different efficiences. Many organisms have two AP endonucleases, usually one is the dominant AP endonuclease, the other has weak AP endonuclease activity; for example, Ape1 and Ape2 in humans. Ape1 is found in this subfamily, it exhibits strong AP-endonuclease activity but shows weak 3'-5' exonuclease and 3'-phosphodiesterase activities. Class II AP endonucleases have been classified into two families, designated ExoIII and EndoIV, based on their homology to the Escherichia coli enzymes exonuclease III (ExoIII) and endonuclease IV (EndoIV). This subfamily belongs to the ExoIII family; the EndoIV family belongs to a different superfamily.	1.66238e-154
NZ_LN831776.1|WP_020433258.1|3679300_3682687_+|hypothetical-protein	gnl|CDD|225990	COG3459, COG3459, Cellobiose phosphorylase [Carbohydrate transport and metabolism].	0
NZ_LN831776.1|WP_020433255.1|3676803_3678969_+|beta-glucosidase-BglX	gnl|CDD|185053	PRK15098, PRK15098, beta-glucosidase BglX.	0
NZ_LN831776.1|WP_046503289.1|3672477_3673722_+|sugar-ABC-transporter-substrate-binding-protein	gnl|CDD|270450	cd14747, PBP2_MalE, Maltose-binding protein MalE; possesses type 2 periplasmic binding fold. This group includes the periplasmic maltose-binding component of an ABC transport system from the phytopathogen Xanthomonas citri and its related bacterial proteins. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	2.25764e-121
NZ_LN831776.1|WP_020433249.1|3674797_3675622_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	8.64871e-84
NZ_LN831776.1|WP_039786834.1|3665426_3666140_+|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	1.11984e-72
NZ_LN831776.1|WP_020427276.1|3658760_3659879_+|citrate-synthase/methylcitrate-synthase	gnl|CDD|99862	cd06109, BsCS-I_like, Bacillus subtilis (Bs) citrate synthase CS-I_like. CS catalyzes the condensation of acetyl coenzyme A (AcCoA) and oxalacetate (OAA) to form citrate and coenzyme A (CoA), the first step in the citric acid cycle (TCA or Krebs cycle). 2MCS catalyzes the condensation of propionyl-coenzyme A (PrCoA) and OAA to form 2-methylcitrate and coenzyme A (CoA) during propionate metabolism. The overall CS reaction is thought to proceed through three partial reactions and involves both closed and open conformational forms of the enzyme: a) the carbanion or equivalent is generated from AcCoA by base abstraction of a proton, b) the nucleophilic attack of this carbanion on OAA to generate citryl-CoA, and c) the hydrolysis of citryl-CoA to produce citrate and CoA. This group contains proteins similar to BsCS-I, one of two CS isozymes in the gram-positive B. subtilis. The majority of CS activity in B. subtilis is provided by the other isozyme, BsCS-II (not included in this group). BsCS-I has a lower catalytic activity than BsCS-II, and has a Glu in place of a key catalytic Asp residue. This change is conserved in other members of this group. For E. coli CS (not included in this group), site directed mutagenesis of the key Asp residue to a Glu converts the enzyme into citryl-CoA lyase which cleaves citryl-CoA to AcCoA and OAA. A null mutation in the gene encoding BsCS-I (citA) had little effect on B. subtilis CS activity or on sporulation. However, disruption of the citA gene in a strain null for the gene encoding BsCS-II resulted in a sporulation deficiency, a characteristic of strains defective in the Krebs cycle. This group contains proteins which functions exclusively as either a CS or a 2MCS, as well as those with relaxed specificity which have dual functions as both a CS and a 2MCS. Many of the gram-negative species represented in this group have a second CS isozyme which is in another group.	1.14402e-162
NZ_LN831776.1|WP_046503281.1|3670287_3671424_+|DUF4179-domain-containing-protein	gnl|CDD|379369	pfam13786, DUF4179, Domain of unknown function (DUF4179).	1.33399e-07
NZ_LN831776.1|WP_020428465.1|3669761_3670298_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|213752	TIGR02954, RNA_polymerase_ECF-type_sigma_factor, RNA polymerase sigma-70 factor, TIGR02954 family. This group of sigma factors are members of the sigma-70 family (TIGR02937). They and appear by homology, tree building, bidirectional best hits and one-to-a-genome distribution, to represent a conserved family. This family is found in certain Bacillus and Clostridium species.	8.30583e-44
NZ_LN831776.1|WP_020427266.1|3667620_3668853_+|aminopeptidase	gnl|CDD|376723	pfam02073, Peptidase_M29, Thermophilic metalloprotease (M29).	0
NZ_LN831776.1|WP_046503285.1|3671486_3672041_-|GNAT-family-N-acetyltransferase	gnl|CDD|227915	COG5628, COG5628, Predicted acetyltransferase [General function prediction only].	4.81188e-18
NZ_LN831776.1|WP_046503275.1|3663048_3664182_-|VanZ-family-protein	gnl|CDD|377417	pfam04892, VanZ, VanZ like family. This family contains several examples of the VanZ protein, but also contains examples of phosphotransbutyrylases.	3.41694e-17

Protein sequences

>NZ_LN831776.1|WP_020427266.1|3667620_3668853_+|aminopeptidase
MLDFDVMLEKYADLVVRVGVNVQPGQVLMIHSPLETAELTRLIVGKAYEAGAKYVLVDWDDEKVTRIRYEKAADDSFGYYPQWQADMLEGFAEEGGAILHIKVPDPELFRGIDSSKVSTAVKAAAVARKKYQNYTRNNKISWSLIKAPTKAWADKVYAGLPEEERVAAMWEAVFQMNRVGSGDPVAAWREHIADLKKSQDRMNAKRYKSLHYRAPGTDLHVELPEGHLWRGGGGENASGVYFVANMPTEEVYTMPHRKGVNGTVSSTLPLNLNGRLVDGITITFTDGKVTAYDAESGREHLTSLLETDEGASYLGEVALVPHDSPISRLNTVFYNTGIDENASCHFALGSAYPSNIEGGTSLSSEELLERGANVSLTHVDFMVGSAELDIDGELADGTVEPVFRKGNWVL
>NZ_LN831776.1|WP_039786833.1|3666140_3667484_+|HAMP-domain-containing-histidine-kinase
MRTIRGKMLLSFFLALVVTVGITVALFVRLIDDILVNQVKTQLHGQAEKAEKILQDSDISRLNNTEFKYVVKGMMLNADYLILDANNKIIDANEDQGVGTTLHYALSERQGIAVLHGKKILYTKERLSGRPYSIFIYAPLSSLRALYGSLMRTTLLAIGFSFFMILAIGLLTVSRVVRPLNRLKEAVSRYEPYRSQDAVFPVDDTTEIGELITTFQSMSERIQQHQRNQVEFLQNVSHELKTPLMSIHGFVFAIQDQVVTQETGLDVIMNQSLRLIDMVDKLLQLSRLEAVDEHWPISEIDLRTMAEEAALLLMPAANARGVALKVEGESLLTVAAGEQLFQVLVNLLQNAVRHTSSQIRVQIEAGYPGAGWAIHIDDDGNGLSEAEREAVFQRFYTGPNGVTGLGLAICRQIAANLDGELTYSSSPLGGARFSFIKYEGRLAGTGG
>NZ_LN831776.1|WP_039786834.1|3665426_3666140_+|response-regulator-transcription-factor
MGTIVVVDDDLFILQLLSEYLRKEAYEVTSFSSGANLVEYVRSEEPECLILDIMMPGIDGLSLLTELRSFTEIPIIMISARGEESDRIHGLELGCSDFLSKPFNPRELVGRVKAMLRLYRMGNGASGDSAAPIKPDHICHAGNLKIYADYRRVTVDGTDISLTSREFELLLFLASHIERPFGREQLIQHVWNYDFFGDVRVVDDLVKRIRKKLAEHGSTLLINTVWGFGYKAAVSKI
>NZ_LN831776.1|WP_052741461.1|3664865_3665276_+|hypothetical-protein
MNNKWTRKAIALLAVMSVVGGSASAFAASAPAPVKTTIASKAAAPAAKTLTAAPAVKHSTPVVKHSAPAVTASTSGKTTAKPAVSKTTAKATKPATKKTTVKAATKPASKKTAVKAAAKPAAKATAAAPAVKSKKK
>NZ_LN831776.1|WP_046503278.1|3664400_3664748_+|hypothetical-protein
MEKKVQQYYKLKAKHKEMEKELSGLRQDILAYCTEKGEADSEIGGYRVKLITQNRKEYDDEKLFQTLADPEVWRLISKADPAKIASLAKLNIIDEDKIAHTYVLKTITILQVDKK
>NZ_LN831776.1|WP_046503275.1|3663048_3664182_-|VanZ-family-protein
MFQSYLFPISNAFMSFPVAALVFTLPFLVVQYRRHGYINKVRAVVLYLLLLYLLNAFYLIMLPMPASRHNAAPVGSIIQHVPLQFIQEIRRNSNIDPGNFLSYFSIFRQPDFLLAAFNVVLTVPFGLFLGYYFRTRWVMCILLSFGLSLLFEVTQITGIYGFFDHPYRIFDVDDLITNTLGGVLGYRIALWISALLPRIEQLDSKVDYSAKRVTYTRRGIAWMLDLPIWMIPFLTLHSWGMQGAYWITTAVYFVLLPCCTGGRTFGKWVVRISISGQDGRSRLWGLIVRYVLQYGVLIGANVFLTTPSTLTSLPSPWTGIPYSLVMLLDFMFLIHLIIRVFKRNPVLVYEQLSKTQSRITWPDKQQTSAENLVEDSI
>NZ_LN831776.1|WP_046503272.1|3661484_3662948_-|serine-hydrolase
MENLITRPLPRSLPEAQGISSAAISAFLKHMEKQRLGLHSFMLLRHGAVVAEAWWSPYRPELPHSLYSLSKSFTSTAIGLAVAEGLLTVEDKVVSFFPEDAPADISPNLANMNISHLLMMGTGHTEDTTSFMENSEDGNWVKAFLQLPVGKTPGTHFLYNTGATYMLSAILQKVSGLTLLEYLEPRLFAPLGIHNPAWTSCPRGINKGGYGLSVTTEDIAAFGQLYLQQGVWNNRQLLPKEWVAAAASKQIDNNDGSPGASSSDWSKGYGYQFWRCRHNAYRGDGAFGQFCIVMPEQDAVIAITSGGSDMQSILNGVWDILLPGMSMEPEAVESDPAAHAELAQLLAHLSIQPVQLQKASTLEETLNGKVYRLKDHPQQLASLALSFTATEAVLTLQGRYGEQTVKLGRGEWAESSAKILDHKNNLIMSSFTWTDENKLKMTLLLVETPFCLTFEVSVREDSIVLKQQFNVSMSAEDLEAEFIGRLA
>NZ_LN831776.1|WP_020427274.1|3660643_3661420_+|exodeoxyribonuclease-III
MTKLVSWNVNGLRACVSKGFMNYFKEAEADIFCVQETKLQEGQILLDLGEAYEQYWNYAVKKGYSGTAVFTKIKPLSVRYGMEVDSEPEGRMITLEFNGFYLVNVYTPNAKRDLTRLDYRMEWEDRFRSYLQELDKRKPVLVCGDLNVAHQEIDLKNAKANRGNSGFTDEERGKMTELLESGFIDSFRHLHPDQEGAYTWWSYMPKIRERNVGWRIDYFLASSRLAPQLKMAGIECNVMGSDHCPVVLQLEDTPQLSV
>NZ_LN831776.1|WP_020427275.1|3660187_3660475_-|hypothetical-protein
MSILLPQQFFNLAPSVGKSYYENLDGILNGAVIVNNASTFPVDLVIYRVNAPSVTYSIPALNSLSITVNALQVAALISTAAGAVFGTIEIATSDF
>NZ_LN831776.1|WP_020427276.1|3658760_3659879_+|citrate-synthase/methylcitrate-synthase
MAKVTGLEGVVAGETDIGLVDGERGYLVYRGYWAKELAVTRCYEEVAFLLWNGYLPSAEELEQLKNEMAASRKLPEYIRRIIELLPASVPMMLVLQSTVAALGEQGNAAWPPAQGEAVRLAAILPTIIAYRYRTLNGLTPLEPLPELGHAANYLYMLTGEKPTEAHVKALSAYQILCMEHGMNASTFAARVVLSTESDMYASVAGAIGAMKGPLHGGAPYEVISMLEAIGTKERAEPWLRNALENGNKLMGFGHRIYKTKDPRAEALQIATQEMIGTDPSFDLALHVEAAAIRLLEEYKPGRRLFTNVEFYAAAILKALELSPDIFTPTFTAGRIIGWTAHIIEQAANNRIFRPQSIYTGPMPRNEFYIERT
>NZ_LN831776.1|WP_020428465.1|3669761_3670298_+|sigma-70-family-RNA-polymerase-sigma-factor
MVSPNAEMKKLTGAVPREDNAFYDAVMEHSDQLYHIAYSYLRNRSDALEAVQEATCRAWIKRATLKDPQAFKPWIIRILIYVCIDEQRRRKRSVPTPEAAMREPVMQDSSSKLEMLWAVEQVKPKYRHVLLLKYYNDMTLTEIADLLGKPEGTIKTWQHKGLKQLRTIMKNRGEWNDQ
>NZ_LN831776.1|WP_046503281.1|3670287_3671424_+|DUF4179-domain-containing-protein
MISSSEEQALLADAVYMQGEPDKDVGSAALRSAVQTGMERGQQRMKNRVFSRGMGFSVMAAVAAAAVLFILPYLHSAPQPVSTRQSVDWGELEVFKGNAVSSLDQPTLDSAIQNGYIQMVNQKAEAEGYSITLNAITADENKIMYLYTAATDDKQEIYSINSAKLKDSATDRYLNATGQVGGNVTVPEPEKNHVFYGRGVVELDRTEPFPQQLEAEFRIASVNPGKLADRRTGTIMADMHYSPVLKVRFALDPKFQEYKTQIVKPNLPFTLNGHEVVLSQVEMSPLLIRARVALKNPAENGWETREDIFENTLFQGITSKVQRESVQLSPVSGNGTEDGFEYSFASNWLNNPESLVLKIKERNSFDKADIQLEIYNKK
>NZ_LN831776.1|WP_046503285.1|3671486_3672041_-|GNAT-family-N-acetyltransferase
MNIETTLTTLKDAYIIKNMYPLYLHDLSGHYGLTDGPVLNEHGIFEDSPEVRTLAEQYDVQNIWWEKPGCLYPFLIRADGRPAGFALVATPPHCAKGVDYFMNDFFVLQPYRGQGYAQQAALQVFGRFAGVWELFTNPAAKNVIGQKFWRKTVSDYTNGIYEEKAGDTFDGYKLSFRFNNAKIK
>NZ_LN831776.1|WP_046503289.1|3672477_3673722_+|sugar-ABC-transporter-substrate-binding-protein
MKKKTGLVITSALLGFSLVAAGCGSSKNESASSDNKTLKVWFMGTADTVTPIAKMYEEKNPGIKVEVQAIPWDNAHDKLLTAVASKNGPDVVQMGTTWIPEFAAAGALKDMAPYIEKYPSMKAENFFDGAVQTTKYQDKTVAIPFYVETRAMFYRTDLLGEVGYPEGPKTWDELKDASKKLVAKGGAGHYALPIEAKDSIYTAIFAWQNGSELIDSNRKPQFNQPAYVETINFLKSFYDEGLSPKGTDLDTVAAFKDGTMGMFISGPWMIQTVKEKAPEIDGKWAVTTLPAKKTNTSSIGGADLSIFNYSKNPDEAAKFIAFMAEQDAQLKFYETSNSMPALKAAWENDALKDPMIQAFGKQLENSRPAPMVTEYEEIAKAAMASFEQITVGGADTQTELDKLNAKANELLGNK
>NZ_LN831776.1|WP_020433247.1|3673854_3674754_+|sugar-ABC-transporter-permease
MSSFVKQWHKNKYPYMFIAPAVILLTLFSIIPIIIALFISFTDMDLVGLADYSNISSAGFANYINIFKDPVFLKSMYNTMIYVVIGVPLVVVASMGVALLLNYGTGWLFKSFRVIYYMPSITNIVAVAVVWGYLYNGSYGLFNYILSIFGLPAQQWLQDPTLAKLSLILLAFWKSIGLNMIIFLAALQGIPRSYYEAAEIDGATGWKKLRFITVPLLGFATFFVTITTLIGWIQFFEEPLVMTKGGPLNATMSMALFIYNNGFQLSKFGYAAAGSFVLFIIIIIVTLIQFAVKKKEVEY
>NZ_LN831776.1|WP_020433249.1|3674797_3675622_+|carbohydrate-ABC-transporter-permease
MALRTKHIEKGLMIALLIIGGLLMMVPFIWMIGSSFKPENEFTVIPPTLFPSHPTFSNYRDLFVKMDFVIYLKNTLIIVLCSFVGLFLNAMAGYAFAKFDFPGKNKFFYIILATMMIPGQVTMIPTYLIINQLHLVNTMAGIVLPGLVGAFAIFLFRQFMTTIPIDLLEAARLDGAGELRIFFQLMVPIVKPVFAVQGILTFIGAWNSFLWPLIIANDERLYTLSVGLSLLKGQYGTEFGLQMAGAAFMVVPIIIIFIFFQKHIIEGYTISGIK
>NZ_LN831776.1|WP_046503294.1|3675665_3676658_+|LacI-family-DNA-binding-transcriptional-regulator
MATIKDVAKLAGVALSTASYAMSGDSKVSAKTREKVLEAARQLNYQKNGFAMDLKRSRTNTIALILTDLSGPYYSELIRSIQDVALSNSYDLIACSSMGGKDSTAVRFLLEKRVDGAIVLAHNITDEILQAAGSSRFPIVVMDRLIAGEGLINVVVDGELGGYSATRYLIDKGHQHIAYISGPANSYDNALRYKGFMRAMHEAGLEEKAKWKLNGGFIREGGYKSTKMMLMQGELPSAIFYANDEMAVGGMKALEEGGISVPEDISVIGFDDIQLAEYIQPPLTTIRQPMYESGSLASHLLFQMLNGDTVNDFYKLKIELVERQSVLPQK
>NZ_LN831776.1|WP_020433255.1|3676803_3678969_+|beta-glucosidase-BglX
MTEHLYHKYVKHMTLEEKIAQLLQLAAPFYDEPGDESEITGPMEELGIKYDTKRAVGSVLGIAGAKKMMAVQKEHLAGSRLGIPLLFMADIVHGFKTIFPIPLAIGCSWDPELAEQSAGIAARESAVSGLHVTFAPMVDLVRDARWGRVMESTGEDPYLNAVFAKAFVQGFQGDNLKDDVSRVAACVKHFAAYGLVEGGREYNTVDLSERQLREYYLPAYKAAVDAGVEMVMTSFNTVNGIPATGNRSLMRGLLRDEWGFDGVVISDWAAIKEIIAHGAAEDEKEAAFKAISSGVDIDMMTTSYVNHLPELVAEGLVDEALIDEAVLRILVLKEKLGLFENPMRGADPELEQQIVYSQEHRKVAQRLAEKSSVLLKNDGVLPLQAGQRVALIGPFAASGDILGWWSWQGSQETAVQLGESMQKVSGDPGHVLISEGCSIDTITEAGLAEAVKAAAAADIIVLALGESSEMSGEGGSRSDIRLPEAQLELVREMKKLGKPVVAVLFNGRPLDLHGVYDVADAVLEAWFPGSEGGAALADILYGKVNPSGRLSMSFPYSAGQIPVYYNAYNTGRPKPVEHTDNRYISQYIDIPNEPLLPFGFGLSYTTFAFEGFSLSSDCLSADRPLEARVTVTNTGSMAGTETVQLYIRDMSGETVRPVKELKDFRQVQLLPGESRDVVFQIEESLLRYHHSDLTFSSDPGMFTVYVGANSRDTQSATFRLI
>NZ_LN831776.1|WP_020433258.1|3679300_3682687_+|hypothetical-protein
MTTAPSTKLSIQKGDLTFTFLESGDLYQAFGGKMMINQLLSSSVDGAPGNLYARLHLSGGIQAFPLLGVKSASRFRQDGERLLWQGEIAADQAGTVLDKTIRYQVVFSMADNGVWFWDVTIDGAGVPLDVIYTQDVGIASPGAVTSNEAYLSQYIDHTVFEDTAKGYVVCSRQNQPQDGKFPYLQQGLLNGAAGFSTDGFQFFGLSYKESNEPEALSRAKLANEVYQYEFAFTALQSPQVQLDGQARFTFYGLFREDHPSAITELEYAASVQEAWQQVQSFGSISAEGEWLSPVSVNSRIGAPLQTLPLTEAELDALFPHKFQEERAGGKLLAFFTEGYEHVVLKDKELLVERPHGHILMSGDNARLNPEVITTTSYMYGIFNSQVVIGNTNFNKMMSNARSALNIFKTSGQRIYVYTDDQYHLLTMPSLYEIGFNYVRWYYKTASDTLVITNYTTMDEPEIRLHVRSAGNIAYRFLVTNQITMNVAEYEVPYEVSQDAAEGTLTFRAAKSGTSAEVYPELAYRMHLNGAVYRLGDESILVDGPAQGSASLVVMELEASKEWTLTLQGMLEGKERTLNPVSFETEAARYREFLAGVMNGFKLTQSGGGEGELFKVNALAWWYTHNMLVHYSVPHGLEQYGGAAWGTRDVCQGPVEYFLATHKYEQVREILLTVFAHQYEDDGSWPQWFMFDKYTHIQQEESHGDIIVWPLKVLGDYLRATQDYAVLEVLLPYTRKHSFDFTEQTASLREHALKELNYIKTNFLHDTYLSSYGDGDWDDTLQPANAQLKQYMVSSWTVALTYQTVLGLSNVLENVDAAWSGELRQLAEGIKGDFNRYMLGTDVIPGFLYFEDPADAKLLLHPEDKETGIQYRLLPMTRSMIGELLTPEQMEEHYKLIQEQFLCPDGVRLMNHPAQYAGGVSLHFKRAEQAANFGREIGLQYVHAHIRFVEAMAKTGKRDQVWKGLAVINPIGIRDAVPNAELRQSNAYFSSSDGKFANRYEAQERFAGLHDGSVPVKGGWRIYSSGPGIYMNQLISNVLGIREDGGDLIIDPVLPDELDGTRLDFDYAGAPAAFVYHCSQGVLSHVKVNGQEVQAERLNNPYRLGGLRIKRADFDRLRSAEGTVVDIYM
>NZ_LN831776.1|WP_020433259.1|3683117_3683369_-|hypothetical-protein
MLTLPGLAVFLQENNCDCERIAHETPIRSALDAKQYFDLTKAALDNRLLSMDYIYGGSGDELHTLKIAPAEVVRLNRILAFVV

Crispr_ID: NZ_LN831776_42

• CRISPR_ID: NZ_LN831776_42
• CRISPR_location: 3996200-3996275
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_42

Consensus_repeat	Method
AAATTAGTTACCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_42

>42.1|3996224|28|NZ_LN831776|CRISPRCasFinder
AACCTGCGAGAGAACAGGGGAATCGGGC

CRISPR arrays and Neighbor proteins around NZ_LN831776_42

CRISPR arrays

The CRISPR arrays of NZ_LN831776_42

>merge|NZ_LN831776|42|3996200-3996275|CRISPRCasFinder
AAATTAGTTACCCTTTTTCCACTTAACCTGCGAGAGAACAGGGGAATCGGGCAAATTAGTTGCCCTTTTTCCACTT

>NZ_LN831776|42|43|3996200-3996275|CRISPRCasFinder
AAATTAGTTACCCTTTTTCCACTT	AACCTGCGAGAGAACAGGGGAATCGGGC
AAATTAGTTGCCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_046503595.1|3989887_3990892_+|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_LN831776.1|WP_020426255.1|3988644_3989760_+|5-methyltetrahydropteroyltriglutamate---homocysteine-S-methyltransferase	unknown	unknown	gnl|CDD|180601
NZ_LN831776.1|WP_082118116.1|3984203_3984686_+|SMI1/KNR4-family-protein	unknown	unknown	gnl|CDD|378155
NZ_LN831776.1|WP_020431277.1|3997145_3997580_+|NUDIX-domain-containing-protein	unknown	unknown	gnl|CDD|240039
NZ_LN831776.1|WP_039790537.1|3999961_4000348_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831776.1|WP_020431274.1|4000350_4001523_+|alanyl-tRNA-editing-protein	unknown	unknown	gnl|CDD|225427
NZ_LN831776.1|WP_020426256.1|3987696_3988629_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223656
NZ_LN831776.1|WP_020431278.1|3996817_3996997_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426249.1|3993375_3994929_+|lysine--tRNA-ligase	unknown	unknown	gnl|CDD|234829
NZ_LN831776.1|WP_046501121.1|4002026_4003481_+|transposase	unknown	unknown	gnl|CDD|372705
NZ_LN831776.1|WP_046503591.1|3984978_3985530_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020431276.1|3999120_3999885_+|TSUP-family-transporter	unknown	unknown	gnl|CDD|182593
NZ_LN831776.1|WP_020428381.1|4005809_4006943_+|copper-amine-oxidase-N-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|377924
NZ_LN831776.1|WP_020428383.1|4003996_4005100_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426248.1|3995022_3995742_+|YebC/PmpR-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|237084
NZ_LN831776.1|WP_082118117.1|4007154_4009788_+|hypothetical-protein	unknown	unknown	gnl|CDD|284995
NZ_LN831776.1|WP_046503604.1|3991853_3992948_+|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_LN831776.1|WP_020428382.1|4005103_4005679_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831776.1|WP_046503599.1|3990893_3991841_+|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_039785603.1|3986419_3987538_+|phosphodiester-glycosidase-family-protein	unknown	unknown	gnl|CDD|378342

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_046503595.1|3989887_3990892_+|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	1.10064e-52
NZ_LN831776.1|WP_020426255.1|3988644_3989760_+|5-methyltetrahydropteroyltriglutamate---homocysteine-S-methyltransferase	gnl|CDD|180601	PRK06520, PRK06520, 5-methyltetrahydropteroyltriglutamate--homocysteine S-methyltransferase.	0
NZ_LN831776.1|WP_082118116.1|3984203_3984686_+|SMI1/KNR4-family-protein	gnl|CDD|378155	pfam09346, SMI1_KNR4, SMI1 / KNR4 family (SUKH-1). Proteins in this family are involved in the regulation of 1,3-beta-glucan synthase activity and cell-wall formation. Genome contextual information showed that SMI1 are primary immunity proteins in bacterial toxin systems.	1.95e-05
NZ_LN831776.1|WP_046503604.1|3991853_3992948_+|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	6.01578e-83
NZ_LN831776.1|WP_039790537.1|3999961_4000348_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	6.55112e-11
NZ_LN831776.1|WP_020431274.1|4000350_4001523_+|alanyl-tRNA-editing-protein	gnl|CDD|225427	COG2872, COG2872, Predicted metal-dependent hydrolases related to alanyl-tRNA synthetase HxxxH domain [General function prediction only].	3.4101e-67
NZ_LN831776.1|WP_020426256.1|3987696_3988629_+|LysR-family-transcriptional-regulator	gnl|CDD|223656	COG0583, LysR, Transcriptional regulator [Transcription].	5.21882e-36
NZ_LN831776.1|WP_020428382.1|4005103_4005679_-|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	4.06565e-05
NZ_LN831776.1|WP_020426249.1|3993375_3994929_+|lysine--tRNA-ligase	gnl|CDD|234829	PRK00750, lysK, lysyl-tRNA synthetase; Reviewed.	6.05708e-172
NZ_LN831776.1|WP_046501121.1|4002026_4003481_+|transposase	gnl|CDD|372705	pfam13751, DDE_Tnp_1_6, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis.	1.42559e-13
NZ_LN831776.1|WP_020431276.1|3999120_3999885_+|TSUP-family-transporter	gnl|CDD|182593	PRK10621, PRK10621, hypothetical protein; Provisional.	1.26017e-48
NZ_LN831776.1|WP_020428381.1|4005809_4006943_+|copper-amine-oxidase-N-terminal-domain-containing-protein	gnl|CDD|377924	pfam07833, Cu_amine_oxidN1, Copper amine oxidase N-terminal domain. Copper amine oxidases catalyze the oxidative deamination of primary amines to the corresponding aldehydes, while reducing molecular oxygen to hydrogen peroxide. These enzymes are dimers of identical subunits, each comprising four domains. The N-terminal domain, which is absent in some amine oxidases, consists of a five-stranded antiparallel beta sheet twisted around an alpha helix. The D1 domains from the two subunits comprise the 'stalk' of the mushroom-shaped dimer, and interact with each other but do not pack tightly against each other.	1.59332e-14
NZ_LN831776.1|WP_020426248.1|3995022_3995742_+|YebC/PmpR-family-DNA-binding-transcriptional-regulator	gnl|CDD|237084	PRK12378, PRK12378, YebC/PmpR family DNA-binding transcriptional regulator.	1.33967e-134
NZ_LN831776.1|WP_082118117.1|4007154_4009788_+|hypothetical-protein	gnl|CDD|284995	pfam07693, KAP_NTPase, KAP family P-loop domain. The KAP (after Kidins220/ARMS and PifA) family of predicted NTPases are sporadically distributed across a wide phylogenetic range in bacteria and in animals. Many of the prokaryotic KAP NTPases are encoded in plasmids and tend to undergo disruption to form pseudogenes. A unique feature of all eukaryotic and certain bacterial KAP NTPases is the presence of two or four transmembrane helices inserted into the P-loop NTPase domain. These transmembrane helices anchor KAP NTPases in the membrane such that the P-loop domain is located on the intracellular side.	1.10669e-34
NZ_LN831776.1|WP_020431277.1|3997145_3997580_+|NUDIX-domain-containing-protein	gnl|CDD|240039	cd04683, Nudix_Hydrolase_24, Members of the Nudix hydrolase superfamily catalyze the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+, for their activity and contain a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which functions as a metal binding and catalytic site. Substrates of nudix hydrolases include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance & "house-cleaning" enzymes. Substrate specificity is used to define families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required.	9.23756e-41
NZ_LN831776.1|WP_046503599.1|3990893_3991841_+|AraC-family-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	7.42892e-20
NZ_LN831776.1|WP_039785603.1|3986419_3987538_+|phosphodiester-glycosidase-family-protein	gnl|CDD|378342	pfam09992, NAGPA, Phosphodiester glycosidase. This is a family conserved from bacteria to humans. The structure of a member from Bacteroides has been crystallized and modelled onto the luminal region of the human member of the family, the transmembrane glycoprotein N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase. There is some conservation of potentially functional residues, implying that in the bacterial members this family acts in some way as a phosphodiester glycosidase. The human protein is also present, so the eukaryotic members are likely to be catalyzing the second step in the formation of the mannose 6-phosphate targeting signal on lysosomal enzyme oligosaccharides.	3.21918e-49

Protein sequences

>NZ_LN831776.1|WP_020426248.1|3995022_3995742_+|YebC/PmpR-family-DNA-binding-transcriptional-regulator
MGRKWNNIKEKKASKDANTSKVYAKFGVEIYVAAKKGEPDPESNRALKVVLERAKTYNVPKAIIDRALDKAKGSGDENYVELRYEGFGPSGSMIIIDALTNNVNRTAPLVRSAFSKNGGNMGVSGSVTYMFEPTAVIGLEGKTADEVMELLIEADVDVRDVLEEDEAVIVYAEPDQFHAVQEVFRSAGITDFTVAELTMLPQNYVTLPEDAEAQFEKLIDALEELDDVQQVYHNVDSEE
>NZ_LN831776.1|WP_020426249.1|3993375_3994929_+|lysine--tRNA-ligase
MHWSEKIANRLIESHPEQQTFVCASGISPSGHIHIGNFREIVTTYFVSRALEKAGKQVRFIFSWDDFDRFRKVPLQVDPSFEQYIGRPYTQVPCPYGCHTSYAEHFEQEFEEALQSFGIRPEFIYQSKEYQSRRYAPGILHALRSRGEIYDILMSFKTGEASEADRAAFYPVSIYCGDCGKDSTTVHSFDEDKELLTYSCTCGHHSSLSIPEADNIKLQWKIDWPMRWNLEQVLFEPGGRDHSSETGSYNVASVISERIFGSAPPMYEPYEFIRIKGSFAKMSSSSGNNYTPDDLLKVYAPENILFLFAKYQPGAAFHIGMDEDVLRNYTEFERYRKAYGSLTLTDDIRAALELSLIHPLDEKAPGFGPIAGLLPLIHFDRKLLLEIMTRNGEEVDVQGLEQTAERAEYWIRHWMPQKLVTVNTRRNNSLYETLEAHEQEWLAAFCRLLRTGGMEDEPLMKAIYAICYDEDKKSMKNNQKRLFTLIYQLVLGQETGPRIPVLIQAVGIEKLLALLDF
>NZ_LN831776.1|WP_046503604.1|3991853_3992948_+|Gfo/Idh/MocA-family-oxidoreductase
MSTTYRIGIIGCGGIANGKHLPSLSKLQNVELAAFCDIIEERAEEARQKYGSAEAKVYTQYTELLKDGSLDIVHVLTPNISHAEISIAALEAGKHVMCEKPMAKTAAEAKAMLEAAKRTGKKLTIGYNNRFREDSLYLKQLCEAGELGSIYFAKAHAIRRRAVPTWGVFLDEEKQGGGPLIDIGTHALDLTLWMMDNYQPKVVLGTTHHELSRRENAANAWGPWDPKQFSVEDSAFGMIVMENGATIMLESSWALNSLDVDEAKCSLSGTEAGADMKQGLRINGEKLGRLYTNEIELSAGGVAFYEGRQESAPDTEMRQWIEAIDQDKEPVVTPEQAYVVSRILEALYESSRTGKAIYLNEQGS
>NZ_LN831776.1|WP_046503599.1|3990893_3991841_+|AraC-family-transcriptional-regulator
MIREGAVWSRCSFEKMFEKQDMLERLDICIEWGHYEIKVLRFHLTSFPAGKVIDFHKHAEFEFHFIPRGRGKVILSGQQYSLSEGMLYLTGPGVIHYQEADAGEAMDELCLHVDITAKERKGVDPWEAAEAEETMVKLRALPVVPAYDYHRAMYCFLEAYEACDGKLLGYYTSIKQLVISILLKTIRAYDSGDNRAEAPVRNMAAYRYEYAVQYMEANHKTPVTLDNVAEKLHISSRQLQRIFKQVQPERPFSRILEEIRLQAVCRALEENLSSIEQIAQDSGFTNANYLHAVFRKRLGMTPAAFRALRQQSNSK
>NZ_LN831776.1|WP_046503595.1|3989887_3990892_+|Gfo/Idh/MocA-family-oxidoreductase
MTLRIGVLSLWHVHAWDYIKQVQEHEDTVIAAVWDEDPVRGQAAAGQLNVPFYASLADLLAEDDIDGVIVDAPTRMHTEVLTAAAKAGKHIFTEKVIAATLKEANAILSEVSKQGVTLTVSLPRLYDGYTLAIQEVLRQGLLGTVTYVRVRLSHDGAIAGWLPAHFYNLEDCQGGALIDLGCHPMYLTRLFLGQAVTGVSASFGYVTGKEVEDNAVATLSTDSGAIGVVEAGFVNSHSPFAIEVHGTEGTLLYGTPDQKLLIRTKAAGDFYQEWTEWPLPAPEESAFRQWVAHIQANTFAEDNVQTALELTRLMEAANLAAREGRTILLKALID
>NZ_LN831776.1|WP_020426255.1|3988644_3989760_+|5-methyltetrahydropteroyltriglutamate---homocysteine-S-methyltransferase
MISPVHGSKRNTPPFRYDIVGSFLRPEALKAARSLHLQGEITDGQLHEIENAEISKLLEQEKALGLKAVTDGEFRRSWWHLDFFLGVAGTQKISLDQGRSAKEAVQRAESFRIVGKIAFGDHPMVSQFVELQQMAGDTLAKMTIPSPALFHFVESYNGNEVYPDREALFRDIIQVYQDAIRAFYEAGCRYLQLDDTTWGTLCSGRHRAHLRSRGIDPDQLAQDYVRLINESIAGRPADMTIALHVCRGNFRSTWFAAGGYEPVAEVLFGQAEVDAFFLEYDNERSGDFAPLRFIRDQQVVLGLVTTKHGGLESKEQIIARIEEAARIVPIDQLCLSAQCGFASTEEGNMLTEEEQWDKLRLIIETADEVWV
>NZ_LN831776.1|WP_020426256.1|3987696_3988629_+|LysR-family-transcriptional-regulator
MTLQQLRYAIEIANSGSMNEAAKRLFVSQPSLSNAIKELENELGITIFERNNRGISISAEGVEFLGYARQIIEQTEFMENRYTGKKRSPIYFSVSTQHYPFVVDAFVKLMKENKVTEYNFSLRETQTYEIIEDVRTLRSDLGILYINEGNYKVMNKLFSDGNLKFTPLFNTNPHVYVRAGHMLAGKELITLEDILPYPYITFEQGENNSLHFSEEMLSFTQIEKNIQVTDRATLTHLLLGSDSYTVGTGIMDAELNGDGLVTIPFDSPEMFTVGWIAHKDRKPGEMMSAYIDILNDLVTRNNFDLKSFLL
>NZ_LN831776.1|WP_039785603.1|3986419_3987538_+|phosphodiester-glycosidase-family-protein
MNSSSLPQRSTVRKKKPVRKRKKKSFFRTLFRVFLFGIFLLLAAGGWLYFAPSAQNTRYLIADTLITTQHRYLAKYIIGEEELKERVTAYNQRFEHMGDEKDTHVIKEPAAEEQNKPLVEVEKVSGSGYTGYVMTVNDPTKVRLGVPNKIGSGEKVTSMVARTGAIAGVNGGGFADPNWKGNGFKPIGLVISQGKLFYNGLGGKKSTQIVGLDKQGKMIAGNYTLDELSKMGVQEAVTFQPRIIVNGKGLIKNAAEGWGIAPRTAMGQRADGALLFVVIDGRQPGYSIGANLYDVQQIMLKHGAVIAANLDGGSSTVLVKDNEIVNKPSSQYGERYLPTAFLVFEHPEQAKIRNIWEGLDPSKIDAGKKRSQ
>NZ_LN831776.1|WP_046503591.1|3984978_3985530_+|hypothetical-protein
MITAKDFLEEWKKETYGLVDFDKKVIELFSLTKETKDFLIEAGLPESSPPFLTFESSINGGGVRLTDKYVNVEEVYSKFIYVGYTGSGAPICIDEENDEVIYIDNENDNEEIFINSSISQLAESLIVYVDFIEKIKNVKGKKAYFERNATKELLSWIANRLQKIDSDSLVQGSFWEEELSTFN
>NZ_LN831776.1|WP_082118116.1|3984203_3984686_+|SMI1/KNR4-family-protein
MIKIGENCVLKYGDSKFEQEVIYKSLELSPCTDKNGFNAFDSFFGFDGGLDDVSHKINQYYERIPSFLIPIADDGKGNLICIGVKDGFNEKIYFWYHENELIANVMLNEKKYGNIGLDDYWDNVFLVSDSFVERKRSYLINKDRIDFRTLPFNMEKGCID
>NZ_LN831776.1|WP_020431278.1|3996817_3996997_+|hypothetical-protein
MENHTKPDKNLINTVEELDRVAVTSQEAQQMEQKKLDIRKESLRDDKTTYKKNEQNTYK
>NZ_LN831776.1|WP_020431277.1|3997145_3997580_+|NUDIX-domain-containing-protein
MPEFRLLSVVHTVLISDQQILLLRRCNTGHDDGFYGLPSGRLDGGEQLDEAAARELQEECGAAVHLKDLKMLGVMHIKTFDDERVDFFFTANRWQGEIVNAEPDKCDDLRWFPIDQLPGNMIPFVKQALEHYREGVWFSSHGWE
>NZ_LN831776.1|WP_020431276.1|3999120_3999885_+|TSUP-family-transporter
MEHGSMAMIAILVICGFLAGVIDSVVGGGGLIAIPALLSAGIPLPLLLGSNKLAGTLCSFTSTASFVRSGKINFGLVKFLIPFSIVGAVGGSLTVRQVPSEFLKPLVIVMLIVITVYTLFKKSWGDVSTFSADSRKTLLTGMGIALVIGFYDGFFGPGTGSFLIFAFLMLGFEFVTAAGNAKVLNFASNIASLLTFAAVGSVSLYYGLLLGVPMVIGAIVGSRIAIHKGASYIRPLFITVTVILIGKQIWDTMH
>NZ_LN831776.1|WP_039790537.1|3999961_4000348_+|GNAT-family-N-acetyltransferase
MWPERELDYVKLDDDDDGVHYGLFDGDRLVSAVSLFIVGKEAQFRKFATRTEQQGQGYGSRLLQHVLDEAEQTGVNRIYCNARSHKAAFYKKFGLAEVPGTAFTKGGKEYIIMEKHFGSAGDRNRKEP
>NZ_LN831776.1|WP_020431274.1|4000350_4001523_+|alanyl-tRNA-editing-protein
MTKKLYYESAYLKDWHTSVSQVVEREDGLYLILEETAFYPHGGGQPCDAGTIGGIPVLDVILEENVVLHKVESLPAGSQVSCQLDWNRRFDHMQQHSGQHLLSAVFRELFQAMTLSFHLGNDYATIDLELRELTPDQLAAAEQEVNRQVVLDRNIVSYFVTPEEMASLPLVKLPKVTENIRIVEIEGVEHNACGGTHVSSTGAIGMIKLLRAEKQKGNIRITFKCGGRALDEANDNQRILSALSAKFNTGKDEILDRIGKWEAEQKQLQAEMAVLREQNDIYMAKELLSGLEPETRVVAHIFADKSLKDLQSLATKLTANTELPVLLLTAMENKAVLACSGSAGLSCGAFFKAHLGEFQGKGGGSDKMAQAGFPAWDEVLKFYEFAKVNL
>NZ_LN831776.1|WP_046501121.1|4002026_4003481_+|transposase
MYSIRQEELFSFEDLLLMRPEDKYSQIFEHLNLAPVLHALGKKNNRGRPEELNVPAMIYSLLIAKMEGIEFVSALVRRLRFSEEFRVQCRFTGSNRIPSEASYSRLIHVLEQTGMLEDLQDTLVLSALEEEFVTGMHLALDSSIVEAWDSLFSEAASKRRAARRAKKPSDAPVAQQLQLELTEPESEPVDERPKKPVYPPGRPSAEEKERRRKEREAYEESLGPFEKTIEQMLPYTYDELLAALPRHAARCDKKNAKGRLTSYYGFKANLLVDADCQYILSGLWSSANLNDQRMAVILLKGLLLKFPRLNVKHVLGDKGYDSAAIYQLIHSLGAYPTIPMIHHKEPPKGMNSDYNPVCSQGHTYRYDSFDAKYETLKYTQPSQCKDCPLSGSGCQKVFKIRIQTDLRKHTYPARGSESFTELYKKRTAVERVFAYLKEYFGMKRTRHRGVRARVDFQLSTLAYNLSKFALDKLNQRLRNSQQVA
>NZ_LN831776.1|WP_020428383.1|4003996_4005100_-|hypothetical-protein
MTINILPFPDLVPNPGKLAAIQAIKGTGKDAVSLLALDQNSDLWRIDLHTGRAAMLLHVDIPGLELQEPVQIIVSADERFAAVSGRFGQYAALYDLQDFKLIMLLSRGDYHYDVCTFPLAFAEHEGRTLLIHGSEWNRLDLLDVRSGENMSARQSPSFADGQYPEHSLDYFHGKIHISPQGDWIIDTGWIWHPIASIRSWSLSAWLSNCWESEDGATLRKLGQLMEDWDQPVVWLDPSTLAVWGQLAIDMYEEEEMKDYGEHLSSHFLAIFDVQTGAQKGLFIPVPAYRTKPLINGSMYYPQGQIAAVNGRVVMWGPENGLSILNPDTGETEFSDEKLCPDFYHPYANVFLEIDESGRFAGKQLTFT
>NZ_LN831776.1|WP_020428382.1|4005103_4005679_-|GNAT-family-N-acetyltransferase
MTLEFKTYDKWDDALWAAMEPLYREAFPHGAKPVGILHAMLDKQIAWLHTGYQDGKLAAMAVTGLSGPAGERMLIIDYMAVDAGLRGQGLGRQFLELIRDWAVQKYDIQAVLIEVEAGHTEEDAARVHFWEHCGCIATEYVHQYIWIPEPYRAMVMPLTRDFAITDDGQALFRRITDFHRKSFRKSGDTGV
>NZ_LN831776.1|WP_020428381.1|4005809_4006943_+|copper-amine-oxidase-N-terminal-domain-containing-protein
MRKWKQSLAVFAAIWFALSAGTVHARENGIVLNDKHTPMGSSQIIVEGATWVPLKELADSMGYALSWNQKTATAQLVRPGREVTFTAKSKKVKTNDSLITLPKAPNILKGKVYVPLVSSVSILGGEIWTDKGSGNIMLVDEPRFTSAAIQSRTYWVSQKSGEIFLSASAGSKPESIGTFPLGETPYSLWLQIKSAGNGSDLLLLIDKHYAMFNDFSNGYQALIKNGKVLKQMDYHYIIVSYPHAAEIPTKQLYMTDGKNVQYINADGSLGKLFELEKSTGRSGDFTVEYAAEDIALVRNLEHTELFAVNTRSGETTNLSAKLISSADRKDWDKADGRDPYVVTKMLVLKKREGNVLTFNYTGMMDEKVHQVVYTITK
>NZ_LN831776.1|WP_082118117.1|4007154_4009788_+|hypothetical-protein
MKVVYSQIKWLWGKLLPPMFCVVIAYIVLLILRIYAPSVFSQDYIGYEKQLIILAYIIAALAICWRGLGGFRGAGSGIKNPLQDRFFLLMNGVAAAVVIDHQSNDRNKDWSGPLFSDLYEITFIICLSVLVLLGITLLFTIYRKFRRKVDDNNSTTQHELNFRTESSLGKEGRDALNREAFAGHVAATIEKHTAKTNEGALTIGLYGPWGSGKTSIFDLMEREFDKSKSNPVIVRFQPWFFGKDYMNLIPEFLNKLIDSIKEHSRAYDAGLIRDLKAYRKFLTPISLRPPGLIINFKDLPVNTEFSKEYMDAEDMRKQIVERLKLADIKLIVLIDDLDRLDNKEIQMVFKLVRMIADFPKTTYIIAMDEEIVTNSLAQMYSKDFVRDVGKEYLEKFIQIPLYIPACDPVLLANLGWEMLEPILKAEEILVTPIQVKDILMQMEISPRNLQRLSNLYRLYLPLLHRDVFPLDLLSLLLIKVSKPGLFEFILKHSDFFLGKLKEDKMRTELMDKLKAAYAPYVAPLKKMFPSINYKEIKTEWIIQKRIGTPEHFWTYFMYSMPYQKLSEADMDSFYLALEQGFMEAEKQQSYLVNKTSPHEFHKKLGEKIDLSTDGRNLLLFAYLFTTFNKEYNKERSYSYSYERKTIISLFARLYGSPEEQSALKILFNDNETNLSLLGMIYDQKVGGEGLKQQIKNYLSVHFSYPVLMEHHEEDIERIFTAWSETAEEHQKRKILKAWSMEYGVGATIRFLMIDQPYEDKVLLNSYITVLQYVPIFVIREELGKMEPITSRKMMNEEFKKDSDPYLIILNYMDNTVYDYAIKELTEIYNNNGTPEYSFSQAIEDLCEFGDSERIRDIRSLHTQIQLQNHIQENQIDH

Crispr_ID: NZ_LN831776_43

• CRISPR_ID: NZ_LN831776_43
• CRISPR_location: 4328519-4328593
• CRISPR_type: Unclear
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_43

Consensus_repeat	Method
AAGTGGAATAAGGGACACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_43

>43.1|4328542|29|NZ_LN831776|CRISPRCasFinder
TGCCGAAGTACCCTACCCTCGGGCAGATG

CRISPR arrays and Neighbor proteins around NZ_LN831776_43

CRISPR arrays

The CRISPR arrays of NZ_LN831776_43

>merge|NZ_LN831776|43|4328519-4328593|CRISPRCasFinder
AAGTGGAATAAGGGACACTAATTTGCCGAAGTACCCTACCCTCGGGCAGATGAAGTGGAAAAAGGGACACTAATT

>NZ_LN831776|43|44|4328519-4328593|CRISPRCasFinder
AAGTGGAATAAGGGACACTAATT	TGCCGAAGTACCCTACCCTCGGGCAGATG
AAGTGGAAAAAGGGACACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020432276.1|4331324_4332221_-|phosphate-ABC-transporter-permease-PstA	unknown	unknown	gnl|CDD|223654
NZ_LN831776.1|WP_020431079.1|4324294_4324468_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020432259.1|4338730_4339453_-|7-carboxy-7-deazaguanine-synthase-QueE	unknown	unknown	gnl|CDD|274545
NZ_LN831776.1|WP_020431088.1|4326850_4327864_+|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|223669
NZ_LN831776.1|WP_052741484.1|4334496_4335393_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223656
NZ_LN831776.1|WP_046507097.1|4319749_4321033_+|ATP-synthase-subunit-J	unknown	unknown	gnl|CDD|273349
NZ_LN831776.1|WP_020431090.1|4327806_4328343_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020432274.1|4332217_4333120_-|phosphate-ABC-transporter-permease-subunit-PstC	unknown	unknown	gnl|CDD|223646
NZ_LN831776.1|WP_052741485.1|4337524_4338052_-|cysteine-hydrolase	unknown	unknown	gnl|CDD|238496
NZ_LN831776.1|WP_020432278.1|4330510_4331287_-|phosphate-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224042
NZ_LN831776.1|WP_020431085.1|4325901_4326621_-|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|293807
NZ_LN831776.1|WP_020431078.1|4322836_4324066_+|aminopeptidase	unknown	unknown	gnl|CDD|376723
NZ_LN831776.1|WP_020431081.1|4324587_4325277_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_039790394.1|4325315_4325900_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|379115
NZ_LN831776.1|WP_020432265.1|4335469_4336324_-|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|379312
NZ_LN831776.1|WP_046503974.1|4321567_4322800_+|aminopeptidase	unknown	unknown	gnl|CDD|376723
NZ_LN831776.1|WP_046503980.1|4333218_4334181_-|phosphate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270371
NZ_LN831776.1|WP_020432257.1|4339445_4339928_-|6-carboxytetrahydropterin-synthase	unknown	unknown	gnl|CDD|376501
NZ_LN831776.1|WP_046507102.1|4336355_4337231_-|DMT-family-transporter	unknown	unknown	gnl|CDD|273359
NZ_LN831776.1|WP_039836816.1|4321134_4321422_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020432276.1|4331324_4332221_-|phosphate-ABC-transporter-permease-PstA	gnl|CDD|223654	COG0581, PstA, ABC-type phosphate transport system, permease component [Inorganic ion transport and metabolism].	1.64452e-93
NZ_LN831776.1|WP_020432259.1|4338730_4339453_-|7-carboxy-7-deazaguanine-synthase-QueE	gnl|CDD|274545	TIGR03365, Bsubt_queE, 7-cyano-7-deazaguanosine (preQ0) biosynthesis protein QueE. This uncharacterized enzyme, designated QueE, participates in the biosynthesis, from GTP, of 7-cyano-7-deazaguanosine, also called preQ0 because in many species it is a precursor of queuosine. In most Archaea, it is instead the precursor of a different tRNA modified base, archaeosine. [Protein synthesis, tRNA and rRNA base modification].	3.65589e-132
NZ_LN831776.1|WP_020431088.1|4326850_4327864_+|alpha/beta-hydrolase	gnl|CDD|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	9.30767e-21
NZ_LN831776.1|WP_020432265.1|4335469_4336324_-|class-I-SAM-dependent-methyltransferase	gnl|CDD|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	3.10805e-07
NZ_LN831776.1|WP_046507097.1|4319749_4321033_+|ATP-synthase-subunit-J	gnl|CDD|273349	TIGR00933, Trk_system_potassium_uptake_protein_trkH., potassium uptake protein, TrkH family. The proteins of the Trk family are derived from Gram-negative and Gram-positive bacteria, yeast and wheat. The proteins of E. coli K12 TrkH and TrkG as well as several yeast proteins have been functionally characterized.The E. coli TrkH and TrkG proteins are complexed to two peripheral membrane proteins, TrkA, an NAD-binding protein, and TrkE, an ATP-binding protein. This complex forms the potassium uptake system. [Transport and binding proteins, Cations and iron carrying compounds].	3.7515e-98
NZ_LN831776.1|WP_020432274.1|4332217_4333120_-|phosphate-ABC-transporter-permease-subunit-PstC	gnl|CDD|223646	COG0573, PstC, ABC-type phosphate transport system, permease component [Inorganic ion transport and metabolism].	6.08669e-95
NZ_LN831776.1|WP_052741485.1|4337524_4338052_-|cysteine-hydrolase	gnl|CDD|238496	cd01014, nicotinamidase_related, Nicotinamidase_ related amidohydrolases. Cysteine hydrolases of unknown function that share the catalytic triad with other amidohydrolases, like nicotinamidase, which converts nicotinamide to nicotinic acid and ammonia.	2.23448e-51
NZ_LN831776.1|WP_020432278.1|4330510_4331287_-|phosphate-ABC-transporter-ATP-binding-protein	gnl|CDD|224042	COG1117, PstB, ABC-type phosphate transport system, ATPase component [Inorganic ion transport and metabolism].	1.36485e-168
NZ_LN831776.1|WP_020431085.1|4325901_4326621_-|MBL-fold-metallo-hydrolase	gnl|CDD|293807	cd07721, yflN-like_MBL-fold, uncharacterized subgroup which includes Bacillus subtilis yflN; MBL-fold metallo hydrolase domain. This subgroup includes the uncharacterized Bacillus subtilis yflN protein. Members of this subgroup belong to the MBL-fold metallo-hydrolase superfamily which is comprised mainly of hydrolytic enzymes which carry out a variety of biological functions. The class B metal beta-lactamases (MBLs) from which this fold was named are only a small fraction of the activities which are included in this superfamily. Activities carried out by superfamily members include class B beta-lactamases, hydroxyacylglutathione hydrolases, AHL (acyl homoserine lactone) lactonases, persulfide dioxygenases, flavodiiron proteins, cleavage and polyadenylation specificity factors such as the Int9 and Int11 subunits of Integrator, Sdsa1-like and AtsA-like arylsulfatases, 5'-exonucleases human SNM1A and yeast Pso2p, ribonuclease J and ribonuclease Z, cyclic nucleotide phosphodiesterases, insecticide hydrolases, and proteins required for natural transformation competence. Classical members of the superfamily are di-, or less commonly mono-, zinc-ion-dependent hydrolases, however the diversity of biological roles is reflected in variations in the active site metallo-chemistry.	4.94663e-71
NZ_LN831776.1|WP_020431078.1|4322836_4324066_+|aminopeptidase	gnl|CDD|376723	pfam02073, Peptidase_M29, Thermophilic metalloprotease (M29).	0
NZ_LN831776.1|WP_052741484.1|4334496_4335393_+|LysR-family-transcriptional-regulator	gnl|CDD|223656	COG0583, LysR, Transcriptional regulator [Transcription].	6.75679e-44
NZ_LN831776.1|WP_039790394.1|4325315_4325900_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|379115	pfam13305, WHG, WHG domain. This presumed domain is around 80 amino acids in length. It is found to the C-terminus of a DNA-binding helix-turn-helix domain. This domain may be involved in binding to an as yet unknown ligand that allows a transcriptional regulation response to that molecule. The domain is named WHG after three conserved residues near the C-terminus of the domain.	1.16775e-22
NZ_LN831776.1|WP_046503974.1|4321567_4322800_+|aminopeptidase	gnl|CDD|376723	pfam02073, Peptidase_M29, Thermophilic metalloprotease (M29).	0
NZ_LN831776.1|WP_046503980.1|4333218_4334181_-|phosphate-ABC-transporter-substrate-binding-protein	gnl|CDD|270371	cd13653, PBP2_phosphate_like_1, Substrate binding domain of putative ABC-type phosphate transporter, a member of the type 2 periplasmic binding fold superfamily. This subfamily contains uncharacterized phosphate binding domains found in PstS proteins that serve as initial receptors in the ABC transport of phosphate in eubacteria and archaea. After binding the ligand, PstS interacts with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The PstS proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	3.40553e-92
NZ_LN831776.1|WP_020432257.1|4339445_4339928_-|6-carboxytetrahydropterin-synthase	gnl|CDD|376501	pfam01242, PTPS, 6-pyruvoyl tetrahydropterin synthase. 6-Pyruvoyl tetrahydrobiopterin synthase catalyzes the conversion of dihydroneopterin triphosphate to 6-pyruvoyl tetrahydropterin, the second of three enzymatic steps in the synthesis of tetrahydrobiopterin from GTP. The functional enzyme is a hexamer of identical subunits.	1.61993e-36
NZ_LN831776.1|WP_046507102.1|4336355_4337231_-|DMT-family-transporter	gnl|CDD|273359	TIGR00950, Uncharacterized_inner_membrane_transporter_YicL, Carboxylate/Amino Acid/Amine Transporter. [Transport and binding proteins, Amino acids, peptides and amines].	6.64322e-16

Protein sequences

>NZ_LN831776.1|WP_020431090.1|4327806_4328343_-|hypothetical-protein
MSSWALTSGMELHSYEQHPLERASYSSCGDCSARRIMSDKSYVGGDLNVLNFERVKWGGIRLNHLLYCMLDLELLSREEEFSVSREDLAILERMVAAVESCGPDNTARKLEKRWRDLLPANQHERDVIMEIWGYAGILVPQEEPRKGRGRVAIITPLPTDYFCFNKLSIVSITSSGWS
>NZ_LN831776.1|WP_020431088.1|4326850_4327864_+|alpha/beta-hydrolase
MNQVKSEKKSSKRIWKKLLLIVLSAIILLIGSGFLYEAIASNAAKKQYPAPGKLVDAGGFKLHIHKQGTGSPTIILESGSGETSLSWRDIPDQLAKSATVVSYDRAGYAWSESSPNERTGANIVRELHNALMNEGLPGPYLVVGHSLGGMYARLFTQTYRDDVMGLVLVDARPENDERETAAILKAEKFAGNPSAAILAILKRSGVMRLFQDSLLEGMVAKEDRGKFINVISTPSYFTAKEQEGKLATSTEDAIRGQNFGALPVRIIARGLPQDYASFGFSEAGGKQLEAIWQAGQRSMLQLSTDSKLTIAEKSGHMIIHDQPELVIETILSLLKQK
>NZ_LN831776.1|WP_020431085.1|4325901_4326621_-|MBL-fold-metallo-hydrolase
MRLTQEGQLLQLTWLPRLFPVNCYLVEEKEGLTLIDAAMSFSVQGILDTAAKLNKPINRIILTHAHGDHVGALDELKQRLPSAQVYISERDAALLRGDRSLREGEPQTPIKGSVPTKITTVPDILLQEGDAVGSLTAIATPGHTPGSMSFLDERTGALIAGDALQTFRRTAVAGTVVPFFPFPAMATWNKASALESAVKLLKLSPKVLAVGHGNLLHAPIEHMKYAVEQAEQLQKKAGN
>NZ_LN831776.1|WP_039790394.1|4325315_4325900_-|TetR/AcrR-family-transcriptional-regulator
MSPREGLDTHTLVLAAAEIADEQGIEEVTLAAIAARLGVRSPSLYNHINGLQGLRSLLAVHGLELLNAAIAAASEGLKGDAAIHAMGQAYVDFARKHPGLYETTLRAPEEGNSELVRASEQVLSLIIRLLSCYELDAEDELHAVRGLRSLLHGFAALENKGGFGMPLDTNISLNWLISAFIAGIRSKSSSTGTG
>NZ_LN831776.1|WP_020431081.1|4324587_4325277_-|hypothetical-protein
MSSMEEHGMVTTYEEMKAVIDQLGIVPLAVLIPGHPSVNGLTKAENWHTDTELDPWAWRARFPGEGLAAYGKFIRKKAVLVAREWFPAYAAAAGSTQSLEERYDSGLCSREALTLLQIIRDNQGIETRELRKLADMKAKEKKTAFDNAVTELQGTLDIVISGVKERHNAEGEKNGWNSTSFETAGHWMAENHIPEFKGTRDEAIVWLRNRMEGKWSPASVSWLGKVLSW
>NZ_LN831776.1|WP_020431079.1|4324294_4324468_+|hypothetical-protein
MKESFSHDLDTVKPDRKETDAPTDSSIAASNAIKYTAYIMLLFGFLYFLIAYLAPML
>NZ_LN831776.1|WP_020431078.1|4322836_4324066_+|aminopeptidase
MLSFTQKLENYALLTVKIGINIQPGQTLVVNADIASAELVRLVVRKAYEAGAKLVKVNYTDELVTRTRYELAPSESFLEPPKWQADELEDLAKNGAAFLSVISTNPDLLNGIDPVRIADNQRTAGQAMMPYRELLMGNHVSWSLVAYPSPVWAAKVFPDAPPEQQVELLWDAIFKAVRADQENPVEAWSLHLAGLKQRCDILNAKKYRKLHYTAPGTDLMLELPEGHIWCQAGAVNGRGVPFLANIPTEEVFTAPLKTGANGTVSSTKPLSYSGNIIDRFTLTLENGKVTDFTAEVGQDALASLLAMDEGSAYFGEVALVPYHSPISESGILYFTTLYDENASCHLALGAAYAFTLEQGTAMTKEQLAEHGMNQSLTHVDFMMGSADMNIDGITDEGLAEPIFRNGNWA
>NZ_LN831776.1|WP_046503974.1|4321567_4322800_+|aminopeptidase
MPQLQAQLSKYADLAVRIGVNVQPGQTLIVSAPISAAEFVRLITAKAYAIGASQVKVNWSDEFITRQLFEHAAPEVFTKPPTWFAGEITEFAENGAAFLHVIAEDPDALKGIDSERIANYQKTRGEALTKYRELQMSDKVSWSIVAIPSQAWADKVFPDVPADERVDKLWEAIFHTVRLDREDPVAAWQEHLDTLEQKANVLNAKKYKSLHYIAPGTDLSIELPEGHLWAQGDSINAKGHSFVANMPTEEVFTAPLKTGVNGTVKATKPLSYGGNIIDGFSITFEQGRIVSVAAEQGQEALEYLIGLDEGAKYLGEVALVPHKSPISESNILYFNTLFDENASNHLAIGTAYAFCLEGGKEMNKDELIAHGLNTSVTHVDFMIGSAEMDIYGITVDGTREPVFLKGNWAF
>NZ_LN831776.1|WP_039836816.1|4321134_4321422_-|hypothetical-protein
MNVEIIKAEMKREEDRSFIGRTVFTLENHNSPYEITFFSKRGTEWDYSLSFAGEPGSEEQFLETDSLLENDDDVYNLLLDAALDTQELTEEVEEE
>NZ_LN831776.1|WP_046507097.1|4319749_4321033_+|ATP-synthase-subunit-J
MVLIAAGTILLCLPAASTGARISFIDALFMATSATCVTGLAVIDTGTQLTVFGQIVLLVLFQFGGLGFVTMATLITLVLNKRISLKERLLLQESMNQNSMQGIVRLIQRVLIYSLVIQLSGAILLAARFTVDMSFGKAVYYGLFHSISIFNNAGFDLFGDIHGPFSGLTRYAEDPIVNITSMLLIFLGGIGFIVLSDLIDYPKRKRLTLHSKVVLSASAVLILGGAAVFFWLELNATLKPLHAGGKVMASFLQAITPRSGGVTTIEIPLLRESTQFLMILLMFIGAAPGSTGGGIKITTFAILVVTAYTKIRGKEDIVMFRHRISKENVYRAITMTLLSLMLVVSATMLLSVTESADFLTVLFEAVSAFGTSGITMGLTPNLTTIGKVLVIILMFVGRTGPLTLAYALKPKNSKELYRYPEGNITIG
>NZ_LN831776.1|WP_020432278.1|4330510_4331287_-|phosphate-ABC-transporter-ATP-binding-protein
MGIAEPVVRESFQTEDLSIFYGTYEAVKGISLPFAQNTVTALIGPSGCGKSTFLRSLNRMNDEISGSTTKGSIWIDGVDINAPGTDVIKLRQKIGMVWQKPNPFYKSIYDNIAFGPKYHGIKGKAALDEIVESSLRRAALWDEVKDRLKDSALALSGGQQQRLCIARALSVNPQILLLDEPASALDPVSTGKVEELIKELKEELRIVIVTHNMQQAARISDFTAYFYLGSLVEYDKTEKVFSNPENQMTQEYIMGRFG
>NZ_LN831776.1|WP_020432276.1|4331324_4332221_-|phosphate-ABC-transporter-permease-PstA
MKPRTADKIATALIVFFALLIVAILIGLLGYILVRGLNHISWDFLTSAPQKIRAGGGVGPQLFNSIYLLVLTLIITVPLGLGAGIFMAEYARPGKLTNFIRLIVEVLSSFPSIVVGLFGLLLIVNTFDLGFSLVSGALALTFFNLPLMVRITEQAFRTVPKQQKEAGFALGLSKWKIVTNVLFPVALPTIITGTILSAGRVFGEAAALMFTAGMSSPRLDFSNWNPSSPTSPLNPFRPAETLAVHIWKINSEGLAPDAAQIAAGASAVLVITVLIFNLAARYFGRVIYRKLTASKRMS
>NZ_LN831776.1|WP_020432274.1|4332217_4333120_-|phosphate-ABC-transporter-permease-subunit-PstC
MRVEPKKNKIEKHHLEDFVGRAYMSFCVLLLIVIIVSMVYFVASKGISTFTSGDVKITEFLFGTKWSPEGDAPSYGAFPFIAGSFLVTLIAALIASPLSICAALFMTEIVPGWGKKLLQPVIELLSGIPSVVYGFVGLSVIVPFLRNTFPGQGIGVAAGALVLSVMILPTITSVAADALASLPQNLKESSFALGATRWQTIARVILPTTFPAIMTGVVLGMARAFGEALAVQMVIGNAPFVPKSLFESASTLTSVITLSMGNTTMGSPQNNALWSMALVLMLMTFVFVLLVRMLERRNKI
>NZ_LN831776.1|WP_046503980.1|4333218_4334181_-|phosphate-ABC-transporter-substrate-binding-protein
MQFRKTWVMALALTSVVALSACGSNNGGNNAATNNGGANATATTAPTETSSGADLSGSILASGSTALQPLVEQVAEKFMETNKDVDIQVQGGGSGTGLTQVAEKQVDIGNSDVFAEEKLKDADAEKAKALVDHQVAVVAIAAVSHPDAGVDSLTKQQLVDIFTGKVTNWKEVGGKDQKIQIINRPSSSGTRATFEGFALGTKTEDLQGSIQEDSSGTVKKMIGETPGAIGYLALSYLDDSVKTLKYDGVEPSVDNVVSGKYPVWAYEHMYTNGEPNEIVKAFLDYIMTPEVQTGDVVELGYIPASQMQVSRDVAGTVTKK
>NZ_LN831776.1|WP_052741484.1|4334496_4335393_+|LysR-family-transcriptional-regulator
MNIVKLQIVVLIEKYKKVTDVAAEMGLKQPTVSFHMKSLESELGTPLFQYRSGRVLLTDAGRTLYQYAARIVALTADAERSMKQYSTLASGHLQVEAGYVPGTYLLPKTVSQFVRQYPDLDISLTVQPETAIRERLRSREIQLAVLHSTEGQDSSFETRSLARNEAVLVFAPGHSFGEIKNLSAELLVLEPWIQHEPASFLRGIADEWAQLNGVRVWGHAVLNSPEAIKGMIREGSGVGLFPKAGIKAEAASGSLRYLPLPGIQPDHGEFVLAWRKDHPLTPLQQAFVELAAAPAEEK
>NZ_LN831776.1|WP_020432265.1|4335469_4336324_-|class-I-SAM-dependent-methyltransferase
MNEHEQASNASLPADQAEKQPVVPSSEELWNEDTYTAWTTRFGSPAEAAAKLMKDPAAKLYPLLNYLGEIRGKKIMNLMGSNGMKAVALGLLGAEASVADFSEANARYAGELAEAAGVPLAYTVSDVLKLPEELLNHTYDIVFAEMGIVHYFTDLAPFMDTVCQLLTPGGRFVLRDFHPVTTKLISSKGSTAKVRKHKVSGDYFDTALEEKKVSYSKYLPSSGGAEGAGRHSVVHWRRWTLGEIVTAAAGSGLVIRELAEEPNLSSDIYDKGIPKTFALVAETV
>NZ_LN831776.1|WP_046507102.1|4336355_4337231_-|DMT-family-transporter
MVVGIVAISFSAIFIKWSAAPASVQGMYRLLFTSLLMLPFARPYSGAAFALRRKDWLLLGASGVLLALHFLLWMGSLKYTSVASSTMIMALEPVFIMLGAYILYKDRSTGAAILGLAIAIFGVVLIGWGDIGLSSDNLKGDLLSVGGTVTVAGHLLIGQKLVARMPSYLYSLIVFITAAVVFAIYNLLAGIPFLDYPPREWGIFVLLAVVPTVFGHILFNWLLQFTSATTVSMNILGEPVGASILAFLLLGEQLTGLQWTGGVLVLGGLAVYLLSGRKKAVKVNESLQSAS
>NZ_LN831776.1|WP_052741485.1|4337524_4338052_-|cysteine-hydrolase
MAEPSTALIIIDVQEAMFSYPDMRLHDEEGVMDRIISLLHKARTAGTPVVYIQHTEDQEYTKGTPTWEISSHVTPQEGELIIEKPTWDAFHLTRLHDELQKRGITDLVICGMQSEFCVDTTTRRAFSMGYSSVLVEDAHSTFDNGSLSGGEIVKYHNSVLGGRFAKLRTAQEVEF
>NZ_LN831776.1|WP_020432259.1|4338730_4339453_-|7-carboxy-7-deazaguanine-synthase-QueE
MSKLPVIEIFGPTIQGEGAVIGVKTMFVRTYGCDYRCSWCDSAFTWDGSAKDKVRMLAPEEIMDELAALAGGNFDCVTLSGGNPALIGEGMGRLIQLLHERGIQAAVETQGSRWQNWFYAVDVLTVSPKPPSSGMETDWNMLDGIMDKMKAHGRATHSLKVVVFNDEDYQYAKRVHSRYPGVPFFLQPGNEDVTEEGDISVRLLARLEWLFNLVIADPEMNKARVLPQLHALIWHNKRGK
>NZ_LN831776.1|WP_020432257.1|4339445_4339928_-|6-carboxytetrahydropterin-synthase
MLGEVSVCKIFTFDSAHQLVGHKGKCSNLHGHTYKLEVVLKGKPLAEEGHSDEGFVADFSDIKATVQESLLDHLDHAFLAMGNEPVLETLKNTGSKIALLSFRTTVENMSAYIAYKLIQASLPLYSVKLWETPTSWAEVLAADIPAEGPAYRLYGGCDCE

Crispr_ID: NZ_LN831776_44

• CRISPR_ID: NZ_LN831776_44
• CRISPR_location: 4559930-4560004
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_44

Consensus_repeat	Method
AAATGGAAAAAGGGACACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_44

>44.1|4559953|29|NZ_LN831776|CRISPRCasFinder
TGCCGGAATACCCTATCCTCGGGCAGATG

CRISPR arrays and Neighbor proteins around NZ_LN831776_44

CRISPR arrays

The CRISPR arrays of NZ_LN831776_44

>merge|NZ_LN831776|44|4559930-4560004|CRISPRCasFinder
AAATGGAAAAAGGGACACTAATTTGCCGGAATACCCTATCCTCGGGCAGATGAAGTGGAAAAAGGGACACTAATT

>NZ_LN831776|44|45|4559930-4560004|CRISPRCasFinder
AAATGGAAAAAGGGACACTAATT	TGCCGGAATACCCTATCCTCGGGCAGATG
AAGTGGAAAAAGGGACACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020429376.1|4550739_4551096_-|hypothetical-protein	unknown	unknown	gnl|CDD|238315
NZ_LN831776.1|WP_046507168.1|4563695_4565303_-|tRNA-(N6-isopentenyl-adenosine(37)-C2)-methylthiotransferase-MiaB	unknown	unknown	gnl|CDD|184624
NZ_LN831776.1|WP_046504172.1|4553293_4554322_-|ROK-family-protein	unknown	unknown	gnl|CDD|224851
NZ_LN831776.1|WP_020431774.1|4565519_4566614_-|NADH:flavin-oxidoreductase	unknown	unknown	gnl|CDD|240095
NZ_LN831776.1|WP_020429386.1|4558225_4559455_-|beta-glucanase	unknown	unknown	gnl|CDD|366548
NZ_LN831776.1|WP_020429374.1|4549832_4550711_-|nitrogenase-iron-protein	unknown	unknown	gnl|CDD|273538
NZ_LN831776.1|WP_020429377.1|4551482_4552085_-|DUF1349-domain-containing-protein	unknown	unknown	gnl|CDD|377771
NZ_LN831776.1|WP_020431783.1|4560354_4561827_-|nicotinate-phosphoribosyltransferase	unknown	unknown	gnl|CDD|236426
NZ_LN831776.1|WP_046504184.1|4570528_4571680_-|iron-containing-alcohol-dehydrogenase	unknown	unknown	gnl|CDD|341467
NZ_LN831776.1|WP_020431782.1|4561842_4562385_-|cysteine-hydrolase	unknown	unknown	gnl|CDD|238245
NZ_LN831776.1|WP_052741493.1|4548484_4549831_-|nitrogenase-cofactor-biosynthesis-protein-NifB	unknown	unknown	gnl|CDD|273539
NZ_LN831776.1|WP_020431766.1|4567688_4568945_-|L-rhamnose-isomerase	unknown	unknown	gnl|CDD|179217
NZ_LN831776.1|WP_020431779.1|4563218_4563671_-|membrane-protein	unknown	unknown	gnl|CDD|226923
NZ_LN831776.1|WP_020429385.1|4556794_4557805_-|4Fe-4S-dicluster-domain-containing-protein	unknown	unknown	gnl|CDD|274014
NZ_LN831776.1|WP_020429379.1|4552081_4553281_-|MFS-transporter	unknown	unknown	gnl|CDD|340891
NZ_LN831776.1|WP_046504180.1|4569046_4570501_-|rhamnulokinase	unknown	unknown	gnl|CDD|198349
NZ_LN831776.1|WP_039790629.1|4562397_4563171_-|NUDIX-hydrolase	unknown	unknown	gnl|CDD|223979
NZ_LN831776.1|WP_046504167.1|4547144_4548464_-|O-acetylhomoserine-aminocarboxypropyltransferase/cysteine-synthase	unknown	unknown	gnl|CDD|225428
NZ_LN831776.1|WP_046504175.1|4554461_4556768_-|pyruvate-synthase	unknown	unknown	gnl|CDD|239471
NZ_LN831776.1|WP_020431772.1|4566790_4567636_-|rhamnulose-1-phosphate-aldolase	unknown	unknown	gnl|CDD|131673

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020429376.1|4550739_4551096_-|hypothetical-protein	gnl|CDD|238315	cd00562, NifX_NifB, This CD represents a family of iron-molybdenum cluster-binding proteins that includes NifB, NifX, and NifY, all of which are involved in the synthesis of an iron-molybdenum cofactor (FeMo-co) that binds the active site of the dinitrogenase enzyme. This domain is a predicted small-molecule-binding domain (SMBD) with an alpha/beta fold that is present either as a stand-alone domain (e.g. NifX and NifY) or fused to another conserved domain (e.g. NifB) however, its function is still undetermined.The SCOP database suggests that this domain is most similar to structures within the ribonuclease H superfamily. This conserved domain is represented in two of the three major divisions of life (bacteria and archaea).	9.10796e-21
NZ_LN831776.1|WP_046507168.1|4563695_4565303_-|tRNA-(N6-isopentenyl-adenosine(37)-C2)-methylthiotransferase-MiaB	gnl|CDD|184624	PRK14327, PRK14327, (dimethylallyl)adenosine tRNA methylthiotransferase; Provisional.	0
NZ_LN831776.1|WP_046504172.1|4553293_4554322_-|ROK-family-protein	gnl|CDD|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	6.66884e-18
NZ_LN831776.1|WP_020431774.1|4565519_4566614_-|NADH:flavin-oxidoreductase	gnl|CDD|240095	cd04747, OYE_like_5_FMN, Old yellow enzyme (OYE)-related FMN binding domain, group 5. Each monomer of OYE contains FMN as a non-covalently bound cofactor, uses NADPH as a reducing agent with oxygens, quinones, and alpha,beta-unsaturated aldehydes and ketones, and can act as electron acceptors in the catalytic reaction. Other members of OYE family include trimethylamine dehydrogenase, 2,4-dienoyl-CoA reductase, enoate reductase, pentaerythriol tetranitrate reductase, xenobiotic reductase, and morphinone reductase.	0
NZ_LN831776.1|WP_020429386.1|4558225_4559455_-|beta-glucanase	gnl|CDD|366548	pfam01270, Glyco_hydro_8, Glycosyl hydrolases family 8.	2.12466e-22
NZ_LN831776.1|WP_020429374.1|4549832_4550711_-|nitrogenase-iron-protein	gnl|CDD|273538	TIGR01287, Nitrogenase_iron_protein_2, nitrogenase iron protein. This model describes nitrogenase (EC 1.18.6.1) iron protein, also called nitrogenase reductase or nitrogenase component II. This model includes molybdenum-iron nitrogenase reductase (nifH), vanadium-iron nitrogenase reductase (vnfH), and iron-iron nitrogenase reductase (anfH). The model excludes the homologous protein from the light-independent protochlorophyllide reductase. [Central intermediary metabolism, Nitrogen fixation].	3.67372e-158
NZ_LN831776.1|WP_020429377.1|4551482_4552085_-|DUF1349-domain-containing-protein	gnl|CDD|377771	pfam07081, DUF1349, Protein of unknown function (DUF1349). This family consists of several hypothetical bacterial proteins but contains one sequence from Saccharomyces cerevisiae. Members of this family are typically around 200 residues in length. The function of this family is unknown.	6.41351e-67
NZ_LN831776.1|WP_020431783.1|4560354_4561827_-|nicotinate-phosphoribosyltransferase	gnl|CDD|236426	PRK09243, PRK09243, nicotinate phosphoribosyltransferase; Validated.	0
NZ_LN831776.1|WP_046504184.1|4570528_4571680_-|iron-containing-alcohol-dehydrogenase	gnl|CDD|341467	cd08188, PDDH, 1,3-Propanediol (1,3-PD) dehydrogenase. This family includes 1,3-propanediol (1,3-PD) dehydrogenase, a key enzyme in the microbial production of 1,3-PD that has been previously characterized as the product of dhaT gene in Klebsiella pneumoniae. 1,3-PD dehydrogenase is a member of the family III metal-dependent polyol dehydrogenases, which are shown to require a divalent metal ion for catalysis. However, some members of this family showed a dependence on Fe(2+) or Zn(2+) for activity.	0
NZ_LN831776.1|WP_020431782.1|4561842_4562385_-|cysteine-hydrolase	gnl|CDD|238245	cd00431, cysteine_hydrolases, Cysteine hydrolases; This family contains amidohydrolases, like CSHase (N-carbamoylsarcosine amidohydrolase), involved in creatine metabolism and nicotinamidase, converting nicotinamide to nicotinic acid and ammonia in the pyridine nucleotide cycle. It also contains isochorismatase, an enzyme that catalyzes the conversion of isochorismate to 2,3-dihydroxybenzoate and pyruvate, via the hydrolysis of the vinyl ether bond, and other related enzymes with unknown function.	2.04575e-48
NZ_LN831776.1|WP_052741493.1|4548484_4549831_-|nitrogenase-cofactor-biosynthesis-protein-NifB	gnl|CDD|273539	TIGR01290, FeMo_cofactor_biosynthesis_protein_NifB, nitrogenase cofactor biosynthesis protein NifB. This model describes NifB, a protein required for the biosynthesis of the iron-molybdenum (or iron-vanadium) cofactor used by the nitrogen-fixing enzyme nitrogenase. NifB belongs to the radical SAM family, and the FeMo cluster biosynthesis process requires S-adenosylmethionine. Archaeal homologs lack the most C-terminal region and score between the trusted and noise cutoffs of this model. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other, Central intermediary metabolism, Nitrogen fixation].	2.1632e-174
NZ_LN831776.1|WP_020431766.1|4567688_4568945_-|L-rhamnose-isomerase	gnl|CDD|179217	PRK01076, PRK01076, L-rhamnose isomerase; Provisional.	0
NZ_LN831776.1|WP_020431779.1|4563218_4563671_-|membrane-protein	gnl|CDD|226923	COG4550, COG4550, Predicted membrane protein [Function unknown].	4.61803e-20
NZ_LN831776.1|WP_020429385.1|4556794_4557805_-|4Fe-4S-dicluster-domain-containing-protein	gnl|CDD|274014	TIGR02175, Pyruvate_synthase_subunit_PorC, 2-oxoacid:acceptor oxidoreductase, gamma subunit, pyruvate/2-ketoisovalerate family. A number of anaerobic and microaerophilic species lack pyruvate dehydrogenase and have instead a four subunit, oxygen-sensitive pyruvate oxidoreductase, with either ferredoxins or flavodoxins (H. pylori) used as the acceptor. Several related four-subunit enzymes may exist in the same species. This model describes the gamma subunit. In Pyrococcus furious, enzymes active on pyruvate and 2-ketoisovalerate share a common gamma subunit.	3.66818e-36
NZ_LN831776.1|WP_020429379.1|4552081_4553281_-|MFS-transporter	gnl|CDD|340891	cd17333, MFS_FucP_MFSD4_like, Bacterial fucose permease, eukaryotic Major facilitator superfamily domain-containing protein 4, and similar proteins. This family is composed of bacterial L-fucose permease (FucP), eukaryotic Major facilitator superfamily domain-containing protein 4 (MFSD4) proteins, and similar proteins. L-fucose permease facilitates the uptake of L-fucose across the boundary membrane with the concomitant transport of protons into the cell; it can also transport L-galactose and D-arabinose. The MFSD4 subfamily consists of two vertebrate members: MFSD4A and MFSD4B. The function of MFSD4A is unknown. MFSD4B is more commonly know as Sodium-dependent glucose transporter 1 (NaGLT1), a primary fructose transporter in rat renal brush-border membranes that also facilitates sodium-independent urea uptake. The FucP/MFSD4 family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	3.98066e-45
NZ_LN831776.1|WP_046504180.1|4569046_4570501_-|rhamnulokinase	gnl|CDD|198349	cd07771, FGGY_RhuK, L-rhamnulose kinases; a subfamily of the FGGY family of carbohydrate kinases. This subfamily is predominantly composed of bacterial L-rhamnulose kinases (RhuK, also known as rhamnulokinase; EC 2.7.1.5), which are encoded by the rhaB gene and catalyze the ATP-dependent phosphorylation of L-rhamnulose to produce L-rhamnulose-1-phosphate and ADP. Some uncharacterized homologous sequences are also included in this subfamily. The prototypical member of this subfamily is Escherichia coli RhuK, which exists as a monomer composed of two large domains. The ATP binding site is located in the cleft between the two domains. This model includes both the N-terminal domain, which adopts a ribonuclease H-like fold, and the structurally related C-terminal domain. The presence of divalent Mg2+ or Mn2+ is required for catalysis. Although an intramolecular disulfide bridge is present in Rhuk, disulfide formation is not important to the regulation of RhuK enzymatic activity. Members of this subfamily belong to the FGGY family of carbohydrate kinases.	0
NZ_LN831776.1|WP_039790629.1|4562397_4563171_-|NUDIX-hydrolase	gnl|CDD|223979	COG1051, COG1051, ADP-ribose pyrophosphatase [Nucleotide transport and metabolism].	4.8023e-36
NZ_LN831776.1|WP_046504167.1|4547144_4548464_-|O-acetylhomoserine-aminocarboxypropyltransferase/cysteine-synthase	gnl|CDD|225428	COG2873, MET17, O-acetylhomoserine sulfhydrylase [Amino acid transport and metabolism].	0
NZ_LN831776.1|WP_046504175.1|4554461_4556768_-|pyruvate-synthase	gnl|CDD|239471	cd03376, TPP_PFOR_porB_like, Thiamine pyrophosphate (TPP family), PFOR porB-like subfamily, TPP-binding module; composed of proteins similar to the beta subunit (porB) of the Helicobacter pylori four-subunit pyruvate ferredoxin oxidoreductase (PFOR), which are also found in archaea and some hyperthermophilic bacteria. PFOR catalyzes the oxidative decarboxylation of pyruvate to form acetyl-CoA, a crucial step in many metabolic pathways. Archaea, anaerobic bacteria and eukaryotes that lack mitochondria (and therefore pyruvate dehydrogenase) use PFOR to oxidatively decarboxylate pyruvate, with ferredoxin or flavodoxin as the electron acceptor. The 36-kDa porB subunit contains the binding sites for the cofactors, TPP and a divalent metal cation, which are required for activity.	5.39504e-103
NZ_LN831776.1|WP_020431772.1|4566790_4567636_-|rhamnulose-1-phosphate-aldolase	gnl|CDD|131673	TIGR02624, Rhamnulose-1-phosphate_aldolase, rhamnulose-1-phosphate aldolase. Members of this family are the enzyme RhaD, rhamnulose-1-phosphate aldolase.	1.99873e-150

Protein sequences

>NZ_LN831776.1|WP_020429386.1|4558225_4559455_-|beta-glucanase
MKNQGKRMWHWKSFVLLCLAIFILPAGSAFAAVNKPFPQHTAYTSGTIKPDNVTQTVMDNAVKTKWDAWKAAYLKPAGTGKYYVKYNSAGETVSEAHGYGMLFTVLMAGYDSNAQTYYNGLYNYYTAHPSSIDPYLMSWKQNSSFQNIEGEDSATDGDMDIAFSLLLAHKQWGSSGTVNYLQAANNIINAIMDNEINQSQWTIRLGDWANSGTYNTATRPSDFMLNHLKAFQAATGDSRWQNVTDKTYTIINSLYSGYSSSTGLLPDFVVYSGGVYKPAAAGFLEDANDGNYNYNSCRTPWRIATDYLLTGDNRALNQLNQMNNWIKTKVNSTPGNIKDGYKLNGSTFGSYNSGAFYAPFGVSAMTSSSNQAWLNSLWSHTSGSAAEDYYEDSIKLFSMIVMSGNWWTY
>NZ_LN831776.1|WP_020429385.1|4556794_4557805_-|4Fe-4S-dicluster-domain-containing-protein
MVQLPIVNDLGFFEIRLESIGGLGANLAGKMLAEAGVVGAGLNGVSFSSYGSEKKGSAVKAHIRFCDLNTPIRDTSPVERPHVVGVFHEALAKTVNVTSGILEHSTVLVNSAKSPAELKELLKMKAGTIAVIDATSIALKEKNRVNMAMLGALFRLCPFLDTETMKGVIEKSLGKKYPQAVQSAISTFERGYNEVEFMQFELAAGDSMPEYVRSDIGVLGYDTQPMGGSIINPGSTFLKNLSISRSGMLPAFDLEACIHCAQCDTVCPDQCFVWEERVDRKGRSQMYLTGIDYQYCKGCLKCVGACPTSALSSQREKEGYADSHTVHHQFDLVTQA
>NZ_LN831776.1|WP_046504175.1|4554461_4556768_-|pyruvate-synthase
MAIDYEKEVGSAKVEQKFLYESGNEMAAYAAHQINYHVMGYFPISPSTEVAQFLDTMKASGQHDIMLVPSDGEHSSAGICYGASTAGGRVFNATSAQGYMFMLEQMPVQAGTRMPMVMNLICRSISGPLNIHGDHSDLYFALNTGWPILMCRDPQSVYDMNLMALKLAEHAKVRLPVMVASDGYFTSHQKRRVQAFAHREDVHKFVGEQPPVGFTDTLDRNNPVTVGPYMNEPDYINNRYQQSVAMYNAGEVFEEIAQEFAELTGRYYPMIEQYRMEDADVAVFLMNSASEIIKDVVDQLRLQGIKAGAISPNMIRPFPQKQIAEALKNVKAITVGDRADSVGGHGGNMVNEIKAALFTYGNTTTKVISRIYGLGGKDFYAEDGHHFFQLAMDAVAADRVDIPFDYYGHNPGTPDKAPKRLLKPMSFESLKTGLITVKQNEETGKLSVRVPPVRSLMKKPRRLSPGHGACPGCGIFSGLELFFKGIEGDIVALYHTGCAMVTTTGYPYSAHKSTFIHNLFQNGAATLSGVVEMFWERKRRGELDGLGLKEDFTFVMVTGDGGMDIGMGPAIGAALRGHKMIIVEYDNEGYMNTGAQQSYSTPLGHRTSTSSIGKTQQGKVTQHKDTAQIMAATNIPYVFTGCEAYPQDLLKKAAKAQWYAQNEGLVYGKILIACPLNWMSEDKDGTDIVSLAVESCFFPLYEVEQGTTTITYNPEDKDKRVEVSAWLKTMGKTRHLLKPENEPALRAFESEVQRRWTRLKAKHEHPDL
>NZ_LN831776.1|WP_046504172.1|4553293_4554322_-|ROK-family-protein
MKNIGGNALVIKEVNINLVRRVLKERKQATKRQIAEDTGLSIVTAGSVLEVLVRQNEVLAAGQISSSGGRPARQYIYNDEHALALILFPFEERGGICIRCTVVTLFGRCLYEVNRPVEQVDLACFEAIIDELLNRYPAIQAIGFGLPGAEAGGRLVLSDYEALRGIPVAEHFRERYQKRVIIENDVNAAAIGYHSRTGRAAAASAVYLYFPDRFPPGAGIIINGKLHRGKSGFAGEVANIPLGISWSGSEWQSSPAGLMEAIARLTATVSSVLNPDAVVLYGSFLQVDHLSGIMEQCAGLLPPGAAPQIVLSTDFAADYLDGMIVSTLATLETGLQLTKFEA
>NZ_LN831776.1|WP_020429379.1|4552081_4553281_-|MFS-transporter
MATVFLIIIYLAFISLGLPDSMIGAAWPMMRPDFGAPVDAAGLLSMIVVAGTIVSSLASSVVLNKLGTGKVTFISVAVTAVALLGFSYSPSILWLAVLSFPLGLGAGSIDAGLNNYVATHYKAHHMSWLHCFWGVGAMLGPIIMSRYIAAGDSWRQGFLTVSLIQFALVILLFMALPLWKRAEPADQVPDGQIQQEIISPQVPGTGVLRIKGVKLALTTFLFYCGVEATLGLWGSSFLVNVKELSAATAAGWVSLYYGGITVGRLITGFVTFRFNNRQLIRTGILVSLLGALLLVLPLPAIFSLFGFILVGLGSAPIFPCMLHETPARFGKEHSQKIMGYQMAMAYTGGAFLPPMLGWIAARSSFMILPFMLVGYIIVMLISSEKINAVMKNRKEEVSM
>NZ_LN831776.1|WP_020429377.1|4551482_4552085_-|DUF1349-domain-containing-protein
MRKTVNWQSGVWSNEPVSAKVLDGAFIVEAAEGSDYWEQTMYGFQHDNGHALLASWEDSEAVEVSFSLQGFTELYDQAGIMLWHSSTEWIKAGIELNDGVPHIGAVVTDGYSDWSLSPVPEWTGGVVTIRASRLNDAVVIRARADNHPWRTIRVARFPYETGKKAGPFVCAPTRAGLQVTFTRWAYTAPDKDIHVDPPTD
>NZ_LN831776.1|WP_020429376.1|4550739_4551096_-|hypothetical-protein
MSWRIAVGSADGYAINEHFGRCGRFLIYEIEQDGTYSQIENRSCEWRRGQDGHDVNHLQTAATVLADCAFVLVGQIGPGARAVLYDNGIQAMAVQSPIELALARLALFLISGRESILH
>NZ_LN831776.1|WP_020429374.1|4549832_4550711_-|nitrogenase-iron-protein
MTKKIKQIAIYGKGGIGKSTTTSNISAALSVAGYKVMQFGCDPKSDSTNTLRGGEYIPTVLDTLRDNHAVRAQDVIFEGFNGIYCVEAGGPAPGVGCAGRGIITSVSLLKQQRIFEELDLDFVIYDVLGDVVCGGFAVPVREGIAEHVYTVTSADFMAIYAANNLFKGIQKYSQDGGALLGGVIANSINAPYAKDIVDDFVKRTDTQVVEYVPRSVTVTQSELQGKTTIEAAPDSEQAKVYRNLARKIADHTVSKVPAPLDTQELRQWAAEWGKQLVALESGLVAPAAVGNL
>NZ_LN831776.1|WP_052741493.1|4548484_4549831_-|nitrogenase-cofactor-biosynthesis-protein-NifB
MQVLEGGSAMQDIHRHPCYDELAHEVFARMHVAVAPKCNINCNYCNIKYDCVSESRPGVVSRVLSPGEAYRQVQDTLKVLPQLTVVGIAGPGDPLANPVQTFETFRLLSREMPDLQLCLSTNGLKLPDYLEEIKECGIRHVTVTMNAVDPVIGGLIYHSIYYRGKAYRGKDAAEILISRQLEGIRAVAALGIKVKVNSVLIPGINDGHLLEVSRVVKAAGAFSHNIMPLIISPGSRFERDGRQPPDPELTLKVQEDSSRVLPVMRHCRQCRADAVGLLGEDRSGGVLSALPVYTLEERENELQKLDNELQVRRDRRQNGTAPGSGGIRIAVASRGGGKVNQHFGHAREFLVYEVKAESARLLGVRRIQAYCNGTAACAGEEQGAGILKETVEMLRDCRLLLCAGIGPVPQEVLHRAEITVIVTKDAIESSLVKYGRLLSYFTPGAVPQ
>NZ_LN831776.1|WP_046504167.1|4547144_4548464_-|O-acetylhomoserine-aminocarboxypropyltransferase/cysteine-synthase
MTDKKLGFDTLKVRAGYDSREHNYAVAVPIYQTASYDLGSVERGEKLFGMEEPGYLYTRIGNPTVAVLEQRLTALDKGTGAVAVASGMAAVTYALLNLAEGGGRILTTPRLYGGTFDALKHLYPKFGVHVDFVEDSDDPEAFRRDIGPDTKAILVESISNPNSTVLDIEAIAEAAHDNGIPLVIDNTFGTPYLFDSFAHGADIVIYSATKAIGGHGTTLGGVILENGNFNWANGRFPHFEEPQYLLREAETGRERSILEVFPDAPFTARVRLNYLAYFGAVLGPFDAFLLLQGIETLSERISKQVANALRIVDYLQKHDQVSWVSHPVAEGNPYKGLADKYFPKGAGSIFTFGFNGSEEQSRIFLNAVKLFSYHANVGDARSLIINSPKTTHGELNPEDQKAAGIAPETIRLSIGLEDADDLIRDLEQAFATAFVESLV
>NZ_LN831776.1|WP_020431783.1|4560354_4561827_-|nicotinate-phosphoribosyltransferase
MRRELALHTDKYQINMMYAHWVNGSHKRRAVFEAYFRKLPFGNGFAVFAGLERITQYISELRFTEEDIRYLSEQEENYAPAFLEELLQFHFQGSIYSMKEGALVFPDEPLVRVEGTIMEAQLVETAILNFMNYQTLIATKASRIKQVAPKDTLLEFGTRRAQEADAAVWGARAAYISGFHATSNMLAGKKFGIPTKGTHAHSWVQSFASEQEAFDAYAKVMPDGVTLLVDTFDTLRSGVPHAINTAKMLEAAGKRMNAIRLDSGDLAYLSIQARKMLDEAGLDYVKIVASNDLDENTIMNLKSQGAAIDTWGVGTQLITASDQPSLGGVYKLVEIESPNGEMVPTIKISSNPEKVSTPGKKEVFRIVGPKGKALADYISFPGEQEPRSGRRLKLFNPLHPYLQKYVEKYEAVSMLEPIFVNGFQVYKLPVLDEIRRYHQEQIDLFWPEYLRKLNPEVYRVNLSELVWTRKQQLIAEHMMTDLNDGPNSEI
>NZ_LN831776.1|WP_020431782.1|4561842_4562385_-|cysteine-hydrolase
MRALIVIDFTNDFVDGSLPVGQPAIDIAPRISGLTQAFVDSGDYVVMAVDLHEENDPYHPEAKLFPPHNLRGTAGRELYGSLKDVYEQNRDSIYWMDKTRYSAFCGTDLTLKLRERGITELHLAGVCTDICVLHTAVDAYNKGFSIVVHQDAVASFNPEGHLWALGHFSGSLGAKVVRVE
>NZ_LN831776.1|WP_039790629.1|4562397_4563171_-|NUDIX-hydrolase
MVSENEEQTYNVKKYRTPDGVPADIVMFTLTKRERKTVTKTLPLRELKVMLVKRKKWPYAGMWALPGGFCQEDESIYDAATRELKEETGVDGGHLEYLGVYSKPGRDPRGWIISHAFFALVEEWMLEHRQASDDAGEVGLFTLQEALEELELAFDHHDIITDAYLRIQQQMLQTTIARQFLPHHFTLSELYQVIQTVVPEFKEPNFIRKITSTRSRQGILKEVRDEAGNPVSSNQYSQRPAQLYMFTDHEPLLSIYT
>NZ_LN831776.1|WP_020431779.1|4563218_4563671_-|membrane-protein
MSQEEPRLNDYGMQTYNTRDLIVREDIMGKAKELASLISTSEEVKHFQQAEQKIQNHERVQSLIAAIKKKQKEIVAFESFKNKEMVAKIEREIEVLQDEIDEIPVVNEFQQSQSDINYLLQLVISVIRDTVSEKINVEAGTEAPPSTCGD
>NZ_LN831776.1|WP_046507168.1|4563695_4565303_-|tRNA-(N6-isopentenyl-adenosine(37)-C2)-methylthiotransferase-MiaB
MTRENNSPDLKSGKGGSKDYSKYFDFSDAKVISEEEGKTTYRIKGRTVQINSNPDYKEGKRRGKQDIEVIDFDNAETNKIMEEFREINRHKQHYYSIATYGCQMNEHDTETMKGLLEQMGYLGTEDRNMADIILLNTCAIRENAEDKVFGELGHLKNLKLEKPGLLLGVCGCMSQEEGVVNRIMSKHGFVDMIFGTHNIHRLPQLVKEAYFSKELVVEVWSKEGDIIENLPKKREGMRAWVNIMYGCDKFCTYCIVPFTRGKERSRRPEDVIAEMRELARQGFKEVTLLGQNVNAYGKDFTDIDYTFGDLMDDMRKIDIPRIRFMTSHPRDFDDRLIEVLGKGGNLTEHIHLPVQSGSTAVLKKMSRKYSRETYLELVRKIKASVPDAVLTTDIIVGFPGETEEQFEETLSLVREVGYDMAYTFIYSPREGTPAASMEDNVPPEVKSERLQRLNDLIKEQSRVSNDRMLGETVEVLVEGESKNNPNVLSGRSRANKLVHFEGPKELIGTFVQVRITDTKTWYIKGDCVAEAVSIL
>NZ_LN831776.1|WP_020431774.1|4565519_4566614_-|NADH:flavin-oxidoreductase
MNTDKLFAPFRAGSLTLANRIVMAPMTRVFSPDGVPGEDVAAYYRRRAEGGVGLIVTEGTAINHPSAVSHQNIPNIHGEASLKGWAKVVEEVHAAGGKIVPQLWHVGMARTIGELPNADALPVGPSGLNLAGEQITEPMTKEEISGIVAAFAQAAADAKAVGFDGIELHGAHGYLIDQFFWEKTNKRTDEYGGDLEARTTFAVEIIDACRRAVGPDFPIILRFSQWKAGDYAAKLAQTPEELARFLTPLSNAGVDIFHCSTRRFWLPEFEGSELNLAGWTKKITGKPTITVGSVGLSSEFGSAVTEQNEEDNLDRLMEKLEKAEFDLVAVGRALISDPAWPAKVQSGRKDEIIAFTPEATRTLY
>NZ_LN831776.1|WP_020431772.1|4566790_4567636_-|rhamnulose-1-phosphate-aldolase
MSTSVIESKGYIASVEAPFIREMSEITHHMWSLGWDELNGGNVSCLLDEEEVAKYISIREPLRTIKLTFPVQELAGKYFIVTGSGKYFRNVIKDPEANLGVLRVSGSGESVEVLWGLRDGAVPTSELASHFMSHIERLKVDPSHRIVLHTHATNVIAMTFTHDLDELKFTKTLWEMCTECLVVFPDGVSVIPWMVPGSSDIGRATADKMKDYRVVVWPQHGIFVTGATMDATFGLVETIEKAATVYNLIGGRAIRQKITDRQLADLAAAFRVTPRAGILEG
>NZ_LN831776.1|WP_020431766.1|4567688_4568945_-|L-rhamnose-isomerase
MDQSIINSYNEAKKVYAAHGIHVDEVLEKLAQIKISLHCWQGDDVKGFLFKDKELSGGIAVTGSYPGRAGTPDELRKDLEKALSLIPGKHKVNLHAIYADTDEQVDLDELEPRHFAPWVEWAKEQGLGLDFNPTCFSHPKAADGFTLSHADGEIRSFWIQHCKASRRIAEYFGRELGQPCVTNFWVPDGYKDTPVDRLAPRMRLKDSLDEVFSEEIDPKFNIDAVESKLFGIGSESYVVGSHEFYMGYGLTRGKAICLDAGHFHPTEVISNKLSSILMFSEQLLLHVSRPVRWDSDHVVTLDDELLEIARELVRGDLLGRTNIGLDFFDGSINHIAAWVIGARNTIKALLRAMLEPVAELKAVELAGDYTSRLALTEEFKSYPFGAVWDYYCAQQNTPVREQWLVEVKRYEQEVLAAR
>NZ_LN831776.1|WP_046504180.1|4569046_4570501_-|rhamnulokinase
MNKHIAVDIGASSGRLVVGTLQEGKLSLEEIHRFSNGFKERGGSCFWDIDYLLDQIIVGLRQAKALGITECTLGIDTWAVDYVLLDAAGSRIQEVYAYRDRRTEGVMEEVAAILPPDTVYAKTGIQQLTFNTLYQLYAHDRKELAQADQILLVPDYLYYRLGGRKINEVTNASTTQLLNLQTGDFDSGLLSFLHLRREQFAPLTAPGESLGFVQDSLVRQYDLPRCQLICVATHDTASAVLGVPVQKGRSAAYISSGTWSLLGVELDQPINNPQAMAANYTNEWGAYGTYRFLKNIMGLWLIQEVRRLDGERYSFAGLARLAGEAEGFRSLIPCNATRFLNPGNMIEEIRSACAESGQPVPETPGQLARCIFDSLALSYRSYLQELEELTGTAVEVLQIVGGGANNGLLCQLTADVAGREVLAGPTESTALGNLAVQLIHAGSVANISEARAIIGNSFPMASYTPRPVPQLEELLDRWEALHHH
>NZ_LN831776.1|WP_046504184.1|4570528_4571680_-|iron-containing-alcohol-dehydrogenase
MSTHVYYVPSTNIMGKGCLKEIGPYIQELKLKKALVVTDKFLVKSGIAGKLLAVLDEAGIQYALYDEVKPNPTCKNVHDGLAFLNAQGCDYLISIGGGSPQDTAKAIGIIATNGGHIKDYEGVHKSKNKSLPIVAVNTTAGTSAEVTINYVITDEERKVKMVMVDKNSIATISVNDPELMIDKPAALTAATGMDALTHAIEALVTPGAYPVTDATALAAVELIFANLARTVKNGHDIEAREQMVYAIFLGGLAFNNAGLGYVHAMAHQLGGVYDLPHGVCNAMLLPYVEEENAKHVPEKFRSIAKAIGLQIEGKSDLECADFVIESIKALSKEVGIPSKLSELGVTEVDLDLLAENSMKDACAPGNPFIPTKEEVITLFRKIL

Crispr_ID: NZ_LN831776_45

• CRISPR_ID: NZ_LN831776_45
• CRISPR_location: 4568962-4569048
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_45

Consensus_repeat	Method
AGTTTTGTGAGCATCTGCTCCCT	CRISPRCasFinder

spacers of NZ_LN831776_45

>45.1|4568985|41|NZ_LN831776|CRISPRCasFinder
GATTTGACTACGTTCAAAACTCGCTTCGAAAGCATCCACTT

CRISPR arrays and Neighbor proteins around NZ_LN831776_45

CRISPR arrays

The CRISPR arrays of NZ_LN831776_45

>merge|NZ_LN831776|45|4568962-4569048|CRISPRCasFinder
AGTTTTGTGAGCATCTGCTCCCTGATTTGACTACGTTCAAAACTCGCTTCGAAAGCATCCACTTAGTTTGGTGAGCATCTGCTCCCT

>NZ_LN831776|45|46|4568962-4569048|CRISPRCasFinder
AGTTTTGTGAGCATCTGCTCCCT	GATTTGACTACGTTCAAAACTCGCTTCGAAAGCATCCACTT
AGTTTGGTGAGCATCTGCTCCCT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020431744.1|4578339_4579653_-|[FeFe]-hydrogenase-H-cluster-maturation-GTPase-HydF	unknown	unknown	gnl|CDD|274853
NZ_LN831776.1|WP_046504191.1|4576411_4577827_+|[FeFe]-hydrogenase-H-cluster-radical-SAM-maturase-HydG	unknown	unknown	gnl|CDD|236590
NZ_LN831776.1|WP_046504184.1|4570528_4571680_-|iron-containing-alcohol-dehydrogenase	unknown	unknown	gnl|CDD|341467
NZ_LN831776.1|WP_020429386.1|4558225_4559455_-|beta-glucanase	unknown	unknown	gnl|CDD|366548
NZ_LN831776.1|WP_020431774.1|4565519_4566614_-|NADH:flavin-oxidoreductase	unknown	unknown	gnl|CDD|240095
NZ_LN831776.1|WP_020431741.1|4579649_4581104_-|aspartate-ammonia-lyase	unknown	unknown	gnl|CDD|237031
NZ_LN831776.1|WP_046507168.1|4563695_4565303_-|tRNA-(N6-isopentenyl-adenosine(37)-C2)-methylthiotransferase-MiaB	unknown	unknown	gnl|CDD|184624
NZ_LN831776.1|WP_020431783.1|4560354_4561827_-|nicotinate-phosphoribosyltransferase	unknown	unknown	gnl|CDD|236426
NZ_LN831776.1|WP_020431754.1|4572848_4574135_-|serine-dehydratase-subunit-alpha-family-protein	unknown	unknown	gnl|CDD|226206
NZ_LN831776.1|WP_020431782.1|4561842_4562385_-|cysteine-hydrolase	unknown	unknown	gnl|CDD|238245
NZ_LN831776.1|WP_020429385.1|4556794_4557805_-|4Fe-4S-dicluster-domain-containing-protein	unknown	unknown	gnl|CDD|274014
NZ_LN831776.1|WP_039835841.1|4572032_4572788_+|DeoR/GlpR-transcriptional-regulator	unknown	unknown	gnl|CDD|224268
NZ_LN831776.1|WP_081487287.1|4575317_4576370_+|[FeFe]-hydrogenase-H-cluster-radical-SAM-maturase-HydE	unknown	unknown	gnl|CDD|274880
NZ_LN831776.1|WP_020431779.1|4563218_4563671_-|membrane-protein	unknown	unknown	gnl|CDD|226923
NZ_LN831776.1|WP_020431772.1|4566790_4567636_-|rhamnulose-1-phosphate-aldolase	unknown	unknown	gnl|CDD|131673
NZ_LN831776.1|WP_020431739.1|4581110_4582175_-|GTP-3',8-cyclase-MoaA	unknown	unknown	gnl|CDD|274250
NZ_LN831776.1|WP_039790629.1|4562397_4563171_-|NUDIX-hydrolase	unknown	unknown	gnl|CDD|223979
NZ_LN831776.1|WP_020431753.1|4574372_4575191_+|formate-dehydrogenase-accessory-sulfurtransferase-FdhD	unknown	unknown	gnl|CDD|234823
NZ_LN831776.1|WP_020431737.1|4582207_4582792_-|4Fe-4S-dicluster-domain-containing-protein	unknown	unknown	gnl|CDD|319876
NZ_LN831776.1|WP_020431766.1|4567688_4568945_-|L-rhamnose-isomerase	unknown	unknown	gnl|CDD|179217

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020431744.1|4578339_4579653_-|[FeFe]-hydrogenase-H-cluster-maturation-GTPase-HydF	gnl|CDD|274853	TIGR03918, hydrogenase_maturation_GTPase_HydF, [FeFe] hydrogenase H-cluster maturation GTPase HydF. This model describes the family of the [Fe] hydrogenase maturation protein HypF as characterized in Chlamydomonas reinhardtii and found, in an operon with radical SAM proteins HydE and HydG, in numerous bacteria. It has GTPase activity, can bind an 4Fe-4S cluster, and is essential for hydrogenase activity. [Protein fate, Protein modification and repair].	0
NZ_LN831776.1|WP_046504191.1|4576411_4577827_+|[FeFe]-hydrogenase-H-cluster-radical-SAM-maturase-HydG	gnl|CDD|236590	PRK09613, thiH, thiamine biosynthesis protein ThiH; Reviewed.	0
NZ_LN831776.1|WP_046504184.1|4570528_4571680_-|iron-containing-alcohol-dehydrogenase	gnl|CDD|341467	cd08188, PDDH, 1,3-Propanediol (1,3-PD) dehydrogenase. This family includes 1,3-propanediol (1,3-PD) dehydrogenase, a key enzyme in the microbial production of 1,3-PD that has been previously characterized as the product of dhaT gene in Klebsiella pneumoniae. 1,3-PD dehydrogenase is a member of the family III metal-dependent polyol dehydrogenases, which are shown to require a divalent metal ion for catalysis. However, some members of this family showed a dependence on Fe(2+) or Zn(2+) for activity.	0
NZ_LN831776.1|WP_020429386.1|4558225_4559455_-|beta-glucanase	gnl|CDD|366548	pfam01270, Glyco_hydro_8, Glycosyl hydrolases family 8.	2.12466e-22
NZ_LN831776.1|WP_020431774.1|4565519_4566614_-|NADH:flavin-oxidoreductase	gnl|CDD|240095	cd04747, OYE_like_5_FMN, Old yellow enzyme (OYE)-related FMN binding domain, group 5. Each monomer of OYE contains FMN as a non-covalently bound cofactor, uses NADPH as a reducing agent with oxygens, quinones, and alpha,beta-unsaturated aldehydes and ketones, and can act as electron acceptors in the catalytic reaction. Other members of OYE family include trimethylamine dehydrogenase, 2,4-dienoyl-CoA reductase, enoate reductase, pentaerythriol tetranitrate reductase, xenobiotic reductase, and morphinone reductase.	0
NZ_LN831776.1|WP_020431741.1|4579649_4581104_-|aspartate-ammonia-lyase	gnl|CDD|237031	PRK12273, aspA, aspartate ammonia-lyase; Provisional.	0
NZ_LN831776.1|WP_046507168.1|4563695_4565303_-|tRNA-(N6-isopentenyl-adenosine(37)-C2)-methylthiotransferase-MiaB	gnl|CDD|184624	PRK14327, PRK14327, (dimethylallyl)adenosine tRNA methylthiotransferase; Provisional.	0
NZ_LN831776.1|WP_020431783.1|4560354_4561827_-|nicotinate-phosphoribosyltransferase	gnl|CDD|236426	PRK09243, PRK09243, nicotinate phosphoribosyltransferase; Validated.	0
NZ_LN831776.1|WP_020431754.1|4572848_4574135_-|serine-dehydratase-subunit-alpha-family-protein	gnl|CDD|226206	COG3681, COG3681, L-cysteine desulfidase [Amino acid transport and metabolism].	3.17089e-115
NZ_LN831776.1|WP_020431782.1|4561842_4562385_-|cysteine-hydrolase	gnl|CDD|238245	cd00431, cysteine_hydrolases, Cysteine hydrolases; This family contains amidohydrolases, like CSHase (N-carbamoylsarcosine amidohydrolase), involved in creatine metabolism and nicotinamidase, converting nicotinamide to nicotinic acid and ammonia in the pyridine nucleotide cycle. It also contains isochorismatase, an enzyme that catalyzes the conversion of isochorismate to 2,3-dihydroxybenzoate and pyruvate, via the hydrolysis of the vinyl ether bond, and other related enzymes with unknown function.	2.04575e-48
NZ_LN831776.1|WP_020429385.1|4556794_4557805_-|4Fe-4S-dicluster-domain-containing-protein	gnl|CDD|274014	TIGR02175, Pyruvate_synthase_subunit_PorC, 2-oxoacid:acceptor oxidoreductase, gamma subunit, pyruvate/2-ketoisovalerate family. A number of anaerobic and microaerophilic species lack pyruvate dehydrogenase and have instead a four subunit, oxygen-sensitive pyruvate oxidoreductase, with either ferredoxins or flavodoxins (H. pylori) used as the acceptor. Several related four-subunit enzymes may exist in the same species. This model describes the gamma subunit. In Pyrococcus furious, enzymes active on pyruvate and 2-ketoisovalerate share a common gamma subunit.	3.66818e-36
NZ_LN831776.1|WP_039835841.1|4572032_4572788_+|DeoR/GlpR-transcriptional-regulator	gnl|CDD|224268	COG1349, GlpR, Transcriptional regulators of sugar metabolism [Transcription / Carbohydrate transport and metabolism].	6.97541e-91
NZ_LN831776.1|WP_081487287.1|4575317_4576370_+|[FeFe]-hydrogenase-H-cluster-radical-SAM-maturase-HydE	gnl|CDD|274880	TIGR03956, iron-only_hydrogenase_maturation_rSAM_protein_HydE, [FeFe] hydrogenase H-cluster radical SAM maturase HydE. This model describes the radical SAM protein HydE, one of a pair of radical SAM proteins, along with GTP-binding protein HydF, for maturation of [Fe] hydrogenase in Chlamydomonas reinhardtii and numerous bacteria. [Protein fate, Protein modification and repair].	0
NZ_LN831776.1|WP_020431779.1|4563218_4563671_-|membrane-protein	gnl|CDD|226923	COG4550, COG4550, Predicted membrane protein [Function unknown].	4.61803e-20
NZ_LN831776.1|WP_020431772.1|4566790_4567636_-|rhamnulose-1-phosphate-aldolase	gnl|CDD|131673	TIGR02624, Rhamnulose-1-phosphate_aldolase, rhamnulose-1-phosphate aldolase. Members of this family are the enzyme RhaD, rhamnulose-1-phosphate aldolase.	1.99873e-150
NZ_LN831776.1|WP_020431739.1|4581110_4582175_-|GTP-3',8-cyclase-MoaA	gnl|CDD|274250	TIGR02666, Cyclic_pyranopterin_monophosphate_synthase, molybdenum cofactor biosynthesis protein A, bacterial. The model for this family describes molybdenum cofactor biosynthesis protein A, or MoaA, as found in bacteria. It does not include the family of probable functional equivalent proteins from the archaea. MoaA works together with MoaC to synthesize precursor Z from guanine. [Biosynthesis of cofactors, prosthetic groups, and carriers, Molybdopterin].	2.85854e-138
NZ_LN831776.1|WP_039790629.1|4562397_4563171_-|NUDIX-hydrolase	gnl|CDD|223979	COG1051, COG1051, ADP-ribose pyrophosphatase [Nucleotide transport and metabolism].	4.8023e-36
NZ_LN831776.1|WP_020431753.1|4574372_4575191_+|formate-dehydrogenase-accessory-sulfurtransferase-FdhD	gnl|CDD|234823	PRK00724, PRK00724, formate dehydrogenase accessory sulfurtransferase FdhD.	3.82001e-116
NZ_LN831776.1|WP_020431737.1|4582207_4582792_-|4Fe-4S-dicluster-domain-containing-protein	gnl|CDD|319876	cd10554, HycB_like, HycB, HydN and similar proteins. This family includes HycB, the FeS subunit of a membrane-associated formate hydrogenlyase system (FHL-1) in Escherichia coli that breaks down formate, produced during anaerobic fermentation, to H2 and CO2. FHL-1 consists of formate dehydrogenase H (FDH-H) and the hydrogenase 3 complex (Hyd-3). HycB is thought to code for the [4Fe-4S] ferredoxin subunit of hydrogenase 3, which functions as an intermediate electron carrier protein between hydrogenase 3 and formate dehydrogenase. HydN codes for the [4Fe-4S] ferredoxin subunit of FDH-H; a hydN in-frame deletion mutation causes only weak reduction in hydrogenase activity, but loss of more than 60% of FDH-H activity. This pathway is only active at low pH and high formate concentrations, and is thought to provide a detoxification/de-acidification system countering the buildup of formate during fermentation.	7.03866e-68
NZ_LN831776.1|WP_020431766.1|4567688_4568945_-|L-rhamnose-isomerase	gnl|CDD|179217	PRK01076, PRK01076, L-rhamnose isomerase; Provisional.	0

Protein sequences

>NZ_LN831776.1|WP_020431766.1|4567688_4568945_-|L-rhamnose-isomerase
MDQSIINSYNEAKKVYAAHGIHVDEVLEKLAQIKISLHCWQGDDVKGFLFKDKELSGGIAVTGSYPGRAGTPDELRKDLEKALSLIPGKHKVNLHAIYADTDEQVDLDELEPRHFAPWVEWAKEQGLGLDFNPTCFSHPKAADGFTLSHADGEIRSFWIQHCKASRRIAEYFGRELGQPCVTNFWVPDGYKDTPVDRLAPRMRLKDSLDEVFSEEIDPKFNIDAVESKLFGIGSESYVVGSHEFYMGYGLTRGKAICLDAGHFHPTEVISNKLSSILMFSEQLLLHVSRPVRWDSDHVVTLDDELLEIARELVRGDLLGRTNIGLDFFDGSINHIAAWVIGARNTIKALLRAMLEPVAELKAVELAGDYTSRLALTEEFKSYPFGAVWDYYCAQQNTPVREQWLVEVKRYEQEVLAAR
>NZ_LN831776.1|WP_020431772.1|4566790_4567636_-|rhamnulose-1-phosphate-aldolase
MSTSVIESKGYIASVEAPFIREMSEITHHMWSLGWDELNGGNVSCLLDEEEVAKYISIREPLRTIKLTFPVQELAGKYFIVTGSGKYFRNVIKDPEANLGVLRVSGSGESVEVLWGLRDGAVPTSELASHFMSHIERLKVDPSHRIVLHTHATNVIAMTFTHDLDELKFTKTLWEMCTECLVVFPDGVSVIPWMVPGSSDIGRATADKMKDYRVVVWPQHGIFVTGATMDATFGLVETIEKAATVYNLIGGRAIRQKITDRQLADLAAAFRVTPRAGILEG
>NZ_LN831776.1|WP_020431774.1|4565519_4566614_-|NADH:flavin-oxidoreductase
MNTDKLFAPFRAGSLTLANRIVMAPMTRVFSPDGVPGEDVAAYYRRRAEGGVGLIVTEGTAINHPSAVSHQNIPNIHGEASLKGWAKVVEEVHAAGGKIVPQLWHVGMARTIGELPNADALPVGPSGLNLAGEQITEPMTKEEISGIVAAFAQAAADAKAVGFDGIELHGAHGYLIDQFFWEKTNKRTDEYGGDLEARTTFAVEIIDACRRAVGPDFPIILRFSQWKAGDYAAKLAQTPEELARFLTPLSNAGVDIFHCSTRRFWLPEFEGSELNLAGWTKKITGKPTITVGSVGLSSEFGSAVTEQNEEDNLDRLMEKLEKAEFDLVAVGRALISDPAWPAKVQSGRKDEIIAFTPEATRTLY
>NZ_LN831776.1|WP_046507168.1|4563695_4565303_-|tRNA-(N6-isopentenyl-adenosine(37)-C2)-methylthiotransferase-MiaB
MTRENNSPDLKSGKGGSKDYSKYFDFSDAKVISEEEGKTTYRIKGRTVQINSNPDYKEGKRRGKQDIEVIDFDNAETNKIMEEFREINRHKQHYYSIATYGCQMNEHDTETMKGLLEQMGYLGTEDRNMADIILLNTCAIRENAEDKVFGELGHLKNLKLEKPGLLLGVCGCMSQEEGVVNRIMSKHGFVDMIFGTHNIHRLPQLVKEAYFSKELVVEVWSKEGDIIENLPKKREGMRAWVNIMYGCDKFCTYCIVPFTRGKERSRRPEDVIAEMRELARQGFKEVTLLGQNVNAYGKDFTDIDYTFGDLMDDMRKIDIPRIRFMTSHPRDFDDRLIEVLGKGGNLTEHIHLPVQSGSTAVLKKMSRKYSRETYLELVRKIKASVPDAVLTTDIIVGFPGETEEQFEETLSLVREVGYDMAYTFIYSPREGTPAASMEDNVPPEVKSERLQRLNDLIKEQSRVSNDRMLGETVEVLVEGESKNNPNVLSGRSRANKLVHFEGPKELIGTFVQVRITDTKTWYIKGDCVAEAVSIL
>NZ_LN831776.1|WP_020431779.1|4563218_4563671_-|membrane-protein
MSQEEPRLNDYGMQTYNTRDLIVREDIMGKAKELASLISTSEEVKHFQQAEQKIQNHERVQSLIAAIKKKQKEIVAFESFKNKEMVAKIEREIEVLQDEIDEIPVVNEFQQSQSDINYLLQLVISVIRDTVSEKINVEAGTEAPPSTCGD
>NZ_LN831776.1|WP_039790629.1|4562397_4563171_-|NUDIX-hydrolase
MVSENEEQTYNVKKYRTPDGVPADIVMFTLTKRERKTVTKTLPLRELKVMLVKRKKWPYAGMWALPGGFCQEDESIYDAATRELKEETGVDGGHLEYLGVYSKPGRDPRGWIISHAFFALVEEWMLEHRQASDDAGEVGLFTLQEALEELELAFDHHDIITDAYLRIQQQMLQTTIARQFLPHHFTLSELYQVIQTVVPEFKEPNFIRKITSTRSRQGILKEVRDEAGNPVSSNQYSQRPAQLYMFTDHEPLLSIYT
>NZ_LN831776.1|WP_020431782.1|4561842_4562385_-|cysteine-hydrolase
MRALIVIDFTNDFVDGSLPVGQPAIDIAPRISGLTQAFVDSGDYVVMAVDLHEENDPYHPEAKLFPPHNLRGTAGRELYGSLKDVYEQNRDSIYWMDKTRYSAFCGTDLTLKLRERGITELHLAGVCTDICVLHTAVDAYNKGFSIVVHQDAVASFNPEGHLWALGHFSGSLGAKVVRVE
>NZ_LN831776.1|WP_020431783.1|4560354_4561827_-|nicotinate-phosphoribosyltransferase
MRRELALHTDKYQINMMYAHWVNGSHKRRAVFEAYFRKLPFGNGFAVFAGLERITQYISELRFTEEDIRYLSEQEENYAPAFLEELLQFHFQGSIYSMKEGALVFPDEPLVRVEGTIMEAQLVETAILNFMNYQTLIATKASRIKQVAPKDTLLEFGTRRAQEADAAVWGARAAYISGFHATSNMLAGKKFGIPTKGTHAHSWVQSFASEQEAFDAYAKVMPDGVTLLVDTFDTLRSGVPHAINTAKMLEAAGKRMNAIRLDSGDLAYLSIQARKMLDEAGLDYVKIVASNDLDENTIMNLKSQGAAIDTWGVGTQLITASDQPSLGGVYKLVEIESPNGEMVPTIKISSNPEKVSTPGKKEVFRIVGPKGKALADYISFPGEQEPRSGRRLKLFNPLHPYLQKYVEKYEAVSMLEPIFVNGFQVYKLPVLDEIRRYHQEQIDLFWPEYLRKLNPEVYRVNLSELVWTRKQQLIAEHMMTDLNDGPNSEI
>NZ_LN831776.1|WP_020429386.1|4558225_4559455_-|beta-glucanase
MKNQGKRMWHWKSFVLLCLAIFILPAGSAFAAVNKPFPQHTAYTSGTIKPDNVTQTVMDNAVKTKWDAWKAAYLKPAGTGKYYVKYNSAGETVSEAHGYGMLFTVLMAGYDSNAQTYYNGLYNYYTAHPSSIDPYLMSWKQNSSFQNIEGEDSATDGDMDIAFSLLLAHKQWGSSGTVNYLQAANNIINAIMDNEINQSQWTIRLGDWANSGTYNTATRPSDFMLNHLKAFQAATGDSRWQNVTDKTYTIINSLYSGYSSSTGLLPDFVVYSGGVYKPAAAGFLEDANDGNYNYNSCRTPWRIATDYLLTGDNRALNQLNQMNNWIKTKVNSTPGNIKDGYKLNGSTFGSYNSGAFYAPFGVSAMTSSSNQAWLNSLWSHTSGSAAEDYYEDSIKLFSMIVMSGNWWTY
>NZ_LN831776.1|WP_020429385.1|4556794_4557805_-|4Fe-4S-dicluster-domain-containing-protein
MVQLPIVNDLGFFEIRLESIGGLGANLAGKMLAEAGVVGAGLNGVSFSSYGSEKKGSAVKAHIRFCDLNTPIRDTSPVERPHVVGVFHEALAKTVNVTSGILEHSTVLVNSAKSPAELKELLKMKAGTIAVIDATSIALKEKNRVNMAMLGALFRLCPFLDTETMKGVIEKSLGKKYPQAVQSAISTFERGYNEVEFMQFELAAGDSMPEYVRSDIGVLGYDTQPMGGSIINPGSTFLKNLSISRSGMLPAFDLEACIHCAQCDTVCPDQCFVWEERVDRKGRSQMYLTGIDYQYCKGCLKCVGACPTSALSSQREKEGYADSHTVHHQFDLVTQA
>NZ_LN831776.1|WP_046504184.1|4570528_4571680_-|iron-containing-alcohol-dehydrogenase
MSTHVYYVPSTNIMGKGCLKEIGPYIQELKLKKALVVTDKFLVKSGIAGKLLAVLDEAGIQYALYDEVKPNPTCKNVHDGLAFLNAQGCDYLISIGGGSPQDTAKAIGIIATNGGHIKDYEGVHKSKNKSLPIVAVNTTAGTSAEVTINYVITDEERKVKMVMVDKNSIATISVNDPELMIDKPAALTAATGMDALTHAIEALVTPGAYPVTDATALAAVELIFANLARTVKNGHDIEAREQMVYAIFLGGLAFNNAGLGYVHAMAHQLGGVYDLPHGVCNAMLLPYVEEENAKHVPEKFRSIAKAIGLQIEGKSDLECADFVIESIKALSKEVGIPSKLSELGVTEVDLDLLAENSMKDACAPGNPFIPTKEEVITLFRKIL
>NZ_LN831776.1|WP_039835841.1|4572032_4572788_+|DeoR/GlpR-transcriptional-regulator
MLAAERRKKIIDLVHQDKRVLVSDLSRMFEVTEETIRRDLEKLEKDGILSRTYGGAMLNRHTNEDLPFVTRNALNTDMKRNIALKALDLINDGDTLMVDPSSTAFEFLKLLGNKNNLTVITNSINILHEFASSGMNIISSGGSLRHRSLSLVGPVAHDTIRRYNVDTAVISCKGIDMERGVTDSNEPECELKKYMLRQAQKVVLLADHTKFDKTAFTRLVELSSIDVLITDRRPAESWLTRLAEENIEVLY
>NZ_LN831776.1|WP_020431754.1|4572848_4574135_-|serine-dehydratase-subunit-alpha-family-protein
MLSLLEILHKEVVPAEGCTEPIAVAYAVSLAAELLEEEITSIRLQLSGNIIKNAMGVGIPGTGQTGLPIAAALGAVVGRSHKELEILSNLTPAELKQANSLLDRGLLEVELKDTPEKLYIEAKVYSRNHLATAIIAGEHTHIEFLALDGEKITPPKSKADCGKPGRADSGYAGSVDRIFEFIHTVPFGDLSFLLEGARMNKAISDEGLRGNYGLQVGKKMSQQSAVNLFGNDVASRIIAATAAASDARMDGSAMPVMTTAGSGNQGIACTLPVIALAELLGKDEEKLARALALSNLVTVHIKHYIGRLSPLCGSGIAGGVGANSGIIYLMGGSLAQIKHGIQNTIASLSGMICDGAKSTCALKISTSTNAAIQAATLAMNNIAPTTKDGVIFEEVEDTIRNMERLVQEGLADTDTAILNIMLSKGGAV
>NZ_LN831776.1|WP_020431753.1|4574372_4575191_+|formate-dehydrogenase-accessory-sulfurtransferase-FdhD
MEQHSEQHGSIIRYRSGQLSREEDSIVAEQPVTIKINGEEFVTLVCTPEYIEDMVVGYLASEGIIRGMQDIRQLWTQEEEGFVHVTTDRWNPLHRQLFAKRYVTSCCGSSRHGFVYVNDARTAKSITGVHTLLTFDDCFRLMDEVLSGAELFHRTGGVHCAALCNPEGIVLSRSDIGRHNALDKIYGHCLRTGIDPGNQIIAFSGRISSEILLKAAKIGCEIILSKSAPTGLAVELAEQLGITAVGFIRQNSCNVYSHPERISDLGPLEMKR
>NZ_LN831776.1|WP_081487287.1|4575317_4576370_+|[FeFe]-hydrogenase-H-cluster-radical-SAM-maturase-HydE
MLEQLASGGSVSQQNLADLISHLEGALRRRLYDLAHKARITAYGTAVYLRGLIEFSNICKQNCLYCGLRSGNRTLSRYRLQPEEILDCCREGYTLGYRTFVLQSGEDDWYTTDKLVQLITSVKQQFPDAALTLSVGERDDESYTRLYAAGADRFLLRHETASASLYRALHPTMEYADRRDRLRALQRIGYQVGAGFMVGLPGQSAADLADDLLYLQELQPDMIGIGPFLPHRDTPLRDEQPGTVENTLDMIALARLMVPDALIPATTAMGTAHPNGRERALQAGANVLMPNLSPMSVRAKYMLYNNKICTGDESAQCRFCLEQRVKSAGFHVDMGRGDSLKHLSRSLQEH
>NZ_LN831776.1|WP_046504191.1|4576411_4577827_+|[FeFe]-hydrogenase-H-cluster-radical-SAM-maturase-HydG
MSKVSERRPADFIQDEEIMEALRYGSEAAADPQIIAAILEKAKACKGLSSREAAVLLHVEDKETLEQLYQVSRSIKEQIYGNRIVLFAPLYVSNYCVNNCVYCGYKHSNSEFARSRLNAAEIAEEVKVLQALGHKRLVLEAGEDPRNCSIDYIIDCIRTIYDTKLDNGSIRRINVNIAATTEEDYRRLAAAGIGTYILFQETYHRPSYRNFHPEGPKHDYDWHTTAMDRAMAAGIDDVGIGVLYGLYDHKYDTIAMLKHAEHLEQAFGCGPHTISVPRLRAAENVNLDNYPHLVSDADFARIVAVLRMAVPYTGMILSTREDSEFRDQIIRLGISQISAGSATGVGAYSVNKNKEDTPQFTVGDHRSPMEIIKSLCKDGYVPSYCTACYREGRTGDRFMQLAKSGQIHNVCQPNSLMTFQEYLLDYADEEMRAIGEQTIRENLERIPREGVRKATREQLQRIHAGERDLRF
>NZ_LN831776.1|WP_020431744.1|4578339_4579653_-|[FeFe]-hydrogenase-H-cluster-maturation-GTPase-HydF
MSVNDTPRGERAHIAVFGRRNAGKSSLINAFCGQEVSIVSPVSGTTTDPVYRPMELLPAGPVVLIDTAGLDDTGELGEQRIRQTLQVLKKTDLALLVVDAEAGAGEFERELLQRLAAAGTNVMIVLNKIDKITSDPPSLEERCSQLALRLEAGSSIRLFPVSTMSGSGIGALKRAAADRLAQEEQRFRLVGDLLSPGDVAVLVVPIDKAAPKGRLILPQQQAIRDIMECDALAVVTKEQELSHTLSRLTGKPRIVITDSQVFLKVQADTPPDVPLTSFSILFARYKGDLPRLVSGARSITRLKDGDRVLIAEACTHHRQSDDIGSVKIPRWLREITGRQLLIDHAAGSDFPADLEQYSLIIHCGACMLNRRAMLRRLDEAEAAGVPIVNYGVFIAYVQGVFPRAIEMFPSAMLAWENGGSGNARQSRRPDTMPLPIV
>NZ_LN831776.1|WP_020431741.1|4579649_4581104_-|aspartate-ammonia-lyase
MTDDSAYRMERDALGSLPVPQDAYYGIHTARAKENFAAGGRPANRKLMHAIARVKQAAAKVNGRNHALPQQKVQAILAACEEILDGCLDAHLIVDAYQGGAGTSSNMNVNEVIANRAIELLGGSKGDYSIVHPIDDVNLHQSTNDVYPTALRIAVIPLLRQLAEELASLQEVFQVKEHEYADLLRLGRTQLMDALPILAGQSFGAYAKAAARDRWRLYKAEERLREINIGGTAVGTGMNAPLTYIYTIADELRELTGLGLCRSDFPMDGTQNMDVFVEVSGLLKAAAVNLLKISNDFRLLSSGPAGGIGEYILPAVQAGSSIMPGKVNPVIAEMLGSVAMRVIADDTAVTLAAASGQLELNAFTPVLAEALLESLELLLHGIPLFRERCLSGLKLDEHRCREHVDRSGVLAAATITYLGYDNAAALAKAAAASGRPLEQLLVEGGWMTEKQIQEVLHPLEVTKPGIPGRSGQSGAEHGRRLIPE
>NZ_LN831776.1|WP_020431739.1|4581110_4582175_-|GTP-3',8-cyclase-MoaA
MSDAQALADSFGRIHNYVRISVTDRCNLSCEYCRPDQADAAFSPEPLTFDEIATVVSVLADMGVTKVRLTGGEPLLRPHLEELVARLHAVSGIERIGLTTNGILLASKARVLREAGLTDVNISLDSLQPERFARITGGGDVGRVLHAIGSSLNAGFERVKVNMVVMKGINDDEIESFLQLTLKYPLDIRFIEYMPIGRGTEGWQAGYMPLGGILERCSRAGWAYEPVCSDDPGHGAAPGRDVTMDTTDSGPARYYRIKGAAGQFGLIDPVSRHFCMTCNRLRITASGHIKPCLYWNDEWNVRPYIGEAELLKQLFLRSLEHKPGRHDMPDRLKESGVVRPVQENTVRQMSQIGG
>NZ_LN831776.1|WP_020431737.1|4582207_4582792_-|4Fe-4S-dicluster-domain-containing-protein
MNSFVIADPGLCIGCHTCEVACVSAHSTENMFLQQEENPDFYPRLRVTETDQVTAPVQCRQCEDAPCANVCPNGSITNIGSSISINQDTCIGCKTCMLVCPFGAIAMVPEFRGGQKQVQPGLRSNANGVWARKERLVASKCDLCEESGNGPACVQICPTHALQLVVPDDVSMDTAAKRAASAQTLQQFGGLIRL

Crispr_ID: NZ_LN831776_46

• CRISPR_ID: NZ_LN831776_46
• CRISPR_location: 4598850-4598942
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_46

Consensus_repeat	Method
TCAACTATAGTTATCGCTCACCC	CRISPRCasFinder

spacers of NZ_LN831776_46

>46.1|4598873|47|NZ_LN831776|CRISPRCasFinder
AGTCCCACGAACTCAACTATAGTTATCACTCATCCAATCTCACGAGC

CRISPR arrays and Neighbor proteins around NZ_LN831776_46

CRISPR arrays

The CRISPR arrays of NZ_LN831776_46

>merge|NZ_LN831776|46|4598850-4598942|CRISPRCasFinder
TCAACTATAGTTATCGCTCACCCAGTCCCACGAACTCAACTATAGTTATCACTCATCCAATCTCACGAGCTCAACTATAGTTATCGCTCATCC

>NZ_LN831776|46|47|4598850-4598942|CRISPRCasFinder
TCAACTATAGTTATCGCTCACCC	AGTCCCACGAACTCAACTATAGTTATCACTCATCCAATCTCACGAGC
TCAACTATAGTTATCGCTCATCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020431685.1|4602323_4603160_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_167345642.1|4601234_4602170_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|197666
NZ_LN831776.1|WP_020431713.1|4590782_4591097_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224647
NZ_LN831776.1|WP_020431697.1|4597585_4597945_-|DUF4180-domain-containing-protein	unknown	unknown	gnl|CDD|379371
NZ_LN831776.1|WP_046504210.1|4593024_4593882_+|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_046504213.1|4595578_4596685_+|glycosyl-hydrolase	unknown	unknown	gnl|CDD|369381
NZ_LN831776.1|WP_052741494.1|4607322_4609071_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_046504227.1|4609106_4610705_-|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_046504205.1|4584853_4586998_-|formate-dehydrogenase-subunit-alpha	unknown	unknown	gnl|CDD|130652
NZ_LN831776.1|WP_020431684.1|4603161_4604094_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_020431678.1|4611014_4612775_-|glycoside-hydrolase-family-2	unknown	unknown	gnl|CDD|225789
NZ_LN831776.1|WP_020431683.1|4604179_4605535_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270452
NZ_LN831776.1|WP_020431720.1|4587130_4587481_-|DUF2294-family-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020431677.1|4612832_4613639_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_046504216.1|4597960_4598452_-|PadR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224609
NZ_LN831776.1|WP_020431702.1|4593887_4595330_-|hypothetical-protein	unknown	unknown	gnl|CDD|366008
NZ_LN831776.1|WP_020431682.1|4605894_4607223_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|224567
NZ_LN831776.1|WP_020431711.1|4591303_4592887_-|glycoside-hydrolase-family-43-protein	unknown	unknown	gnl|CDD|350114
NZ_LN831776.1|WP_046504219.1|4598964_4601079_-|beta-xylosidase	unknown	unknown	gnl|CDD|367535
NZ_LN831776.1|WP_020431717.1|4588112_4589009_-|decarboxylating-6-phosphogluconate-dehydrogenase	unknown	unknown	gnl|CDD|236582

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020431685.1|4602323_4603160_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	6.01936e-73
NZ_LN831776.1|WP_020431678.1|4611014_4612775_-|glycoside-hydrolase-family-2	gnl|CDD|225789	COG3250, LacZ, Beta-galactosidase/beta-glucuronidase [Carbohydrate transport and metabolism].	3.02816e-43
NZ_LN831776.1|WP_020431713.1|4590782_4591097_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	3.72791e-34
NZ_LN831776.1|WP_020431697.1|4597585_4597945_-|DUF4180-domain-containing-protein	gnl|CDD|379371	pfam13788, DUF4180, Domain of unknown function (DUF4180).	2.26714e-33
NZ_LN831776.1|WP_046504210.1|4593024_4593882_+|AraC-family-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	4.78282e-27
NZ_LN831776.1|WP_046504213.1|4595578_4596685_+|glycosyl-hydrolase	gnl|CDD|369381	pfam07470, Glyco_hydro_88, Glycosyl Hydrolase Family 88. Unsaturated glucuronyl hydrolase catalyzes the hydrolytic release of unsaturated glucuronic acids from oligosaccharides (EC:3.2.1.-) produced by the reactions of polysaccharide lyases.	6.84727e-17
NZ_LN831776.1|WP_052741494.1|4607322_4609071_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	7.54654e-48
NZ_LN831776.1|WP_046504227.1|4609106_4610705_-|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.96799e-50
NZ_LN831776.1|WP_046504205.1|4584853_4586998_-|formate-dehydrogenase-subunit-alpha	gnl|CDD|130652	TIGR01591, Formate_dehydrogenase_subunit_alpha, formate dehydrogenase, alpha subunit, archaeal-type. This model describes a subset of formate dehydrogenase alpha chains found mainly archaea but also in alpha and gamma proteobacteria and a small number of gram positive bacteria. The alpha chain contains domains for molybdopterin dinucleotide binding and molybdopterin oxidoreductase (pfam01568 and pfam00384, respectively). The holo-enzyme also contains beta and gamma subunits. The enzyme catalyzes the oxidation of formate (produced from pyruvate during anaerobic growth) to carbon dioxide with the concomitant release of two electrons and two protons. The enzyme's purpose is to allow growth on formate in some circumstances and, in the case of FdhH in gamma proteobacteria, to pass electrons to hydrogenase (by which process acid is neutralized). This model is well-defined, with only a single fragmentary sequence falling between trusted and noise. The alpha subunit of a version of nitrate reductase is closely related.	0
NZ_LN831776.1|WP_020431684.1|4603161_4604094_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	4.62281e-91
NZ_LN831776.1|WP_020431683.1|4604179_4605535_-|extracellular-solute-binding-protein	gnl|CDD|270452	cd14749, PBP2_XBP1_like, The periplasmic-binding component of ABC transport systems specific for xylo-oligosaccharides; possesses type 2 periplasmic binding fold. This group represents the periplasmic component of an ABC transport system XBP1 that shows preference for xylo-oligosaccharides in the order of xylotriose > xylobiose > xylotetraose. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	2.55927e-32
NZ_LN831776.1|WP_167345642.1|4601234_4602170_+|helix-turn-helix-domain-containing-protein	gnl|CDD|197666	smart00342, HTH_ARAC, helix_turn_helix, arabinose operon control protein.	1.26182e-24
NZ_LN831776.1|WP_020431677.1|4612832_4613639_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	4.98348e-70
NZ_LN831776.1|WP_046504216.1|4597960_4598452_-|PadR-family-transcriptional-regulator	gnl|CDD|224609	COG1695, COG1695, Predicted transcriptional regulators [Transcription].	3.85464e-10
NZ_LN831776.1|WP_020431702.1|4593887_4595330_-|hypothetical-protein	gnl|CDD|366008	pfam00295, Glyco_hydro_28, Glycosyl hydrolases family 28. Glycosyl hydrolase family 28 includes polygalacturonase EC:3.2.1.15 as well as rhamnogalacturonase A(RGase A), EC:3.2.1.-. These enzymes are important in cell wall metabolism.	4.83405e-09
NZ_LN831776.1|WP_020431682.1|4605894_4607223_-|extracellular-solute-binding-protein	gnl|CDD|224567	COG1653, UgpB, ABC-type sugar transport system, periplasmic component [Carbohydrate transport and metabolism].	4.30898e-29
NZ_LN831776.1|WP_020431711.1|4591303_4592887_-|glycoside-hydrolase-family-43-protein	gnl|CDD|350114	cd09000, GH43_SXA-like, Glycosyl hydrolase family 43, such as Selenomonas ruminantium beta-D-xylosidase SXA. This glycosyl hydrolase family 43 (GH43) includes enzymes that have been characterized to mainly have beta-1,4-xylosidase (beta-D-xylosidase;xylan 1,4-beta-xylosidase; EC 3.2.1.37) activity, including Selenomonas ruminantium (Xsa;Sxa;SXA), Bifidobacterium adolescentis ATCC 15703 (XylC;XynB;BAD_0428) and Bacillus sp. KK-1 XylB. They are part of an array of hemicellulases that are involved in the final breakdown of plant cell-wall whereby they degrade xylan. They hydrolyze beta-1,4 glycosidic bonds between two xylose units in short xylooligosaccharides. These are inverting enzymes (i.e. they invert the stereochemistry of the anomeric carbon atom of the substrate) that have an aspartate as the catalytic general base, a glutamate as the catalytic general acid and another aspartate that is responsible for pKa modulation and orienting the catalytic acid. These enzymes possess an additional C-terminal beta-sandwich domain that restricts access for substrates to a portion of the active site to form a pocket. The active-site pockets comprise of two subsites, with binding capacity for two monosaccharide moieties and a single route of access for small molecules such as substrate. A common structural feature of GH43 enzymes is a 5-bladed beta-propeller domain that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	0
NZ_LN831776.1|WP_046504219.1|4598964_4601079_-|beta-xylosidase	gnl|CDD|367535	pfam03512, Glyco_hydro_52, Glycosyl hydrolase family 52.	0
NZ_LN831776.1|WP_020431717.1|4588112_4589009_-|decarboxylating-6-phosphogluconate-dehydrogenase	gnl|CDD|236582	PRK09599, PRK09599, NADP-dependent phosphogluconate dehydrogenase.	0

Protein sequences

>NZ_LN831776.1|WP_046504216.1|4597960_4598452_-|PadR-family-transcriptional-regulator
MTGYDLKKLIQESSFLYWSGNNNQIYKALVELLNAGFVTNEVRHQDSSPSKKIYTITSSGLAELRKWVVAPPEPPEFKKTFLIQLAWADQLSPDELNVLLAGYEQEVRTQLLLLKGQAGIGNYVNEGNAKGINLWKLIHSNLISTYNNELTWLAELRHELDLT
>NZ_LN831776.1|WP_020431697.1|4597585_4597945_-|DUF4180-domain-containing-protein
MKIESIQKEGQAYVLCRPDDQPLRTEQDVLDLISGCFEHNSYKLLLQEGTLSDEFYNLRTGLAGTTLQKLINYHVKAAAVIHTEEATQGRFKELLTELNKGEDFRVFGSETEALDWLLG
>NZ_LN831776.1|WP_046504213.1|4595578_4596685_+|glycosyl-hydrolase
MSTAYWQEIMDKLDTKVTRMAEQIGGKCPHYAGADGKYDDMASDWWTTGFWPGLLWIMHDMTGKELYKEAAWHWDATLEEWFVKPTVELHHDVGFQFLPTAVIKHTLTGDEDGLRRGIEAANFLAARYNPAGKFIRAWNEDKYGWVIIDCMLNISLLFWASKVTGDPRYKHIAVSHAETTMQYGIREDGSTKHILSFDAETGAYIENFGGQGYSPESCWSRGAAWGLYGFFNTYRHTGDERFLNTAKRIAHYFIAALPDDQVPYWDFRTGDDGRKYKDSSAAAIAASGLLELADVVPPGEKSLYANAAARILRSLTDNYATWDQPEHEAVLTKGTGSGDSFIEVSLIYADYYYIEAVAKLNGWKHRIF
>NZ_LN831776.1|WP_020431702.1|4593887_4595330_-|hypothetical-protein
MNQLQVYEAPNHIPGREDYQVKVRTAGGGWQPLFVYEVKVDMHEVRPASMALFDMEGEAEVEIICLYTEIENVNISPASRSVECSHDRHKISFRLNGPQKLSVEINGGRFRNLHLFANPMEVGAPQPDGAGVHLVQPGIHRSPDLLALMKRTEDQGTGLPQTLYFAPGTHYIEETVFAVPSGTVIYLAGGAAFVGSLSCDRVEDVEIRGRGVVYLAEFHRFSAFRGVRIVFSRRIRVEGITVIDPPHYSIFIGQSTDIAVTNFKSFSTRGWSDGIDIMSSSEVAIRDVFMRNSDDCIAIYGSRWDYFGDSRNISVRDSVLWADVAHPLMIGTHGDYRRGGDIIENIVYENIDILEHHEPQENYWGALAINAGDGNTVRNVLYSNIRVERIEQGQLFDLRVVMNKDYNPEPGKGIEKVTFRNVSFNGGGVHPSRIYGYDEDRGVNGVEFINLQIGGEWVENTRTDLILLNAYAHNVVFKRE
>NZ_LN831776.1|WP_046504210.1|4593024_4593882_+|AraC-family-transcriptional-regulator
MKQLFEPVIFTDRKSLIWDYQIYTDDHYKGYYHWHQCCEVMYVHSGQGNVVVNQQMYDIRSGMLFFFQPYQLHRIYSEVSRECPFVRTIFYIDPHTAENLLSGFAKRKAIFSALWQGRNTYCGFDLSSSAGAVDWIYKNYNLCRNSTMEEDSEDITIMLLQLLSCLGTGENSLIQPEERRNLRYSEQIMSWIEEHYQEEVNLEQLAAETHLSKSYVSRVFHQETGGRLVDYLTARRIKQACRLLSTTDMPVEQIGIAVGFPNASYFNQLFKRVLGTTPLKYRKNN
>NZ_LN831776.1|WP_020431711.1|4591303_4592887_-|glycoside-hydrolase-family-43-protein
MAPTIVNPVLKGFHPDPSFLRVGDDYYIATSTFEWFPGVEIHHSRDLVHWRPLTRVLTESSQVDLRGNSSSGSIWAPALSYDNGIYYLLFTDVKSRKSAYKDLHNYLITAADILGPWSDPVRLNGSGFDPFLFHDADGTQWLLNMRWDFRKQHSNFSGIIMQQYDPKSRSLTGPVHELYKGTPAGVTEGPQLYQRNGYYYLLVAEGGTGINHMVTLARSRSRTGPYETDPDYPVMTTAHDLAFAFQQAGHGSLVETQSGEWYMAHLCTRPIPGTGTMNPLGRETAIQRVVWTDDGWLRLAHGGKLPALAVEGPDLEPHPFPEWPERDDFDYDTLGYPYQSLRVPFDPSWVSLTERPGFLRLRGRESLASLHDQSLIGRPIQHFACTVSTCLEFEPDTFLQMAGLVLYYDDSDYYYLRVTADEIRGVSLGVVMCRAGKYDEITSMQISVKAWDRYYLKAAIDGRDIMFYASPDGEIWTAMCTPLDFGTLSDEYGGKLGFTGAYAGICVQDLDQQAKKAYFDYFEYRAD
>NZ_LN831776.1|WP_020431713.1|4590782_4591097_+|helix-turn-helix-transcriptional-regulator
MIEDVKSLLAGAEHVHQIIGKKWVSLIIHVLNDGPKRFSELNTMIPDLSKRMLNERLKELEEYGLLIRVVIPDRPVRTEYSLTAKGQELGEALGHVEAWALKWL
>NZ_LN831776.1|WP_020431717.1|4588112_4589009_-|decarboxylating-6-phosphogluconate-dehydrogenase
MKVGLIGLGKMGANLGRNLLDHGHEVVAFDVNREAVSELESKGAAGADSLAGLVSKLGVPRIAWIMVPHAFVDSVIEELAPLLSKGDIIIEAGNSQYKESIRRHGELAQQGIYFLDAGTSGGMEGARNGACYMVGGDEEAWAVAEPLFRDTAVQDGYLFAGKPGSGHFLKMVHNGIEYGMMAAIGEGFEVLEKSGFDYNFEQVARVWNNGSVIRSWLMELVERAFSKDAKLDEIKGVMHSSGEGRWTLETAFDLQAATPVIAMALLMRYRSLETDTFTGKVVAALRNEFGGHAVETKD
>NZ_LN831776.1|WP_020431720.1|4587130_4587481_-|DUF2294-family-protein
MSEADFEYQEKIRRLAVKIVKHYRGKGPENVKVKLDNESQITIEIRGILSSLSEILLKEGAADLVAEYWKVLKPYLERGFMEELIETVGCRFSYSWRLCDQYHEGRSVIIQLNKSV
>NZ_LN831776.1|WP_046504205.1|4584853_4586998_-|formate-dehydrogenase-subunit-alpha
MENKVLTVCPYCGSGCQLYLLVENGQVVGAEPADGRTNEGNLCLKGHYGWDFLNDPQLLTSRLRKPMIRKEGVLQEVSWEEAIGFTAEKLNAIKEKYGPDAIMGTGSARGPGNEANYVMQKFMRAVIGTNNIDHCARVCHGPSVAGLTYSLGDGAMSNSIPEIENTDLLLIFGYNAAVTHPIVARRIVKAKQKGAVLIVADPRKTESARIADTWLPLKGGTNMALVNAFGHVLIEEELYDKDYVSNFVQGFDEYKANVEKYTPEYAERITGVRAADIRKVMRQYAKSGKAMILYGMGVCQFAQAVDVVKGLASLALLTGHFGRESVGIGPVRGQNNVQGSCDMGALPNVYPGYQSVEDAKIRKKFEKAWGTSLPDKTGYRLTEVPHLILKENKIKAYYIFGEDPVQSDPNAAELREALDQLELVIVQDIFMNKTALHADVILPATSWGEHDGVYSSADRGFQRIRKAIDPPGDVKPDWQIISEVSTAMGYPMAYKNSEEIWDEMRKLCPSFAGASYSKMEALGGVQWPCPSEDHPGTPYLYQGNRFTTPSGKGQLFACEWRAPLEQPDAEYPLTLSTVREVGHYSVRTMTGNCRALSQLSDEPGNIQISLEDAAEHGIADGQLVQVYSRRGHIMARAQVSGRIKKGATYMTYHFWIGACNELTVDYLDPVSKTPEFKYCAVRIEAISDQAQAEALVRKQYAELRKQMLVGAVPE
>NZ_LN831776.1|WP_046504219.1|4598964_4601079_-|beta-xylosidase
MPKNQFFNAHHSPIGAFASFTLGFKGAAGGFDLEAGKPPRQSIFIGLARKDGNGYDTLPFHEQGGDDESKRYDIENPDPNPDKPRILHPFADEEITRNFSLSVDSWSAGDLTFRIYSPVRAVPDPETASEEELKQILLPALLVELEVDNTASPSARRAFFGFQGNDPYSAMRRLDDMQSGLTGVGQGRFLAIAAEQGTGVKSALHFTMEDILLAELEENWTFGLGHVGAQVIEVPPGVKQCYRFAVCFHRSGFVTTGMDASYYYNRYFSNVESVAEYALAHFAEIKQQAVQANAMLEDSGLSEDQTFMLAHAIRSYYGSTQLLDYNQKPFWIVNEGEYRMMNTFDLTVDQLFYELRMNPWTVRNELDMFVERYSYTDTVRFPGDETDYPGGISFTHDMGVANAVSRAGYSAYEMYGIDGCFSHMTHEQLVNWVLSSAVYLEHTGDRSWMERNLGVLEDCLTSMVNRDHPEPGQRNGVMGLDSSRTMGGAEITTYDSLDVSLGQARNNIYLAGKCWAAYLAMEKIFREAGKPELSATAGDQAERCAATIVVSVTEDGYIPAVIGEGNDSKIIPAIEGLVFPYFTGCREALERDGRFAGYMAALERHLQAVLVKGVCLFEDGGWKISSTSNNSWLSKIYLSQFIARQILGLEWTESGSEADRAHVEWLTHPELSVWSWSDQIISGEITGSKYYPRGVTAILWLDEQ
>NZ_LN831776.1|WP_167345642.1|4601234_4602170_+|helix-turn-helix-domain-containing-protein
MKKRTLMNVNFPGIEHSLDGRMSPDLQAAFHIYAAHWRKVNAQWQYPEHTHPMFEINLVLQGRQHMTVGGQAYLQECGDILFIRPGVRHASLGADAAGDMTYYCLHFDIDDLSLRRTLLTMDAVSLSGESPVLLAIRSALDVMIRTAILTEAEDAQRNRLVRLNASLQLFAALSAWVLSETPAATRSAQPGVTENTVALANAVEGLLQESVFTAAATGSRGGGIEDIAARLGYSPNHCNRAFRHIYGMSPRQYLSGLIIRHAKLMLLDNSLSVEAIAHRLGYRDVSHFSKQFKRWTGLPPMAYRQLTAESK
>NZ_LN831776.1|WP_020431685.1|4602323_4603160_-|carbohydrate-ABC-transporter-permease
MTLQAKKRWGEVALLAVTVLLAVIFFFPIFFNLMSAFKSNAEIMKDAIAFPKGLYLDSFKYLLTETDFPRAIVNSLILTLVSIVAQVLIIPMAGYAIERRDTRWTKMVFLYFLAGMMIPFQAYMIPLFKELRVFGLYGSLAGPILVYVAGAVGFGCLLYTSFVKGIPKEIEEAAEIDGCSRYGIFWKIVFPLLGPVTASMVVLNGLGIWNDFLMPMLVLPSGEPKTMVVEIYRYIGEFSSRWDMIFAGTAMSVVPVLIVFIALQKYFVKGIASGATKG
>NZ_LN831776.1|WP_020431684.1|4603161_4604094_-|sugar-ABC-transporter-permease
MATAAERTDKPLTAAIPQKKRKWQSYALLFILPSFLIYTLFVIVPTVGSIYLSFTSWDGISEDVRYIGFANFAEIWQSPRVHNALKNTLVMTVSLVLLENIAAILLAVLVDKVRWFRNLFRSVFYFPTLLSGIVMGFVWAMILNYNFGVFNQILDAIGLGSWVVDWLGNPKYAMISIILSTVWKGAGYYMIIYLAGLQGIPAELNEAASIDGASGFQQFRHITFPLLAGSMTVCLVLSMISALKIFDQIAVMTDGGPGFETETLTYIIYKVGFGELRQGFGTALAMVLFLIIMLITVIQVKFLRKREVQM
>NZ_LN831776.1|WP_020431683.1|4604179_4605535_-|extracellular-solute-binding-protein
MQKKTITKLSVLLLAATTVLSACGSSNNNSNASGTSGNAAGSPSPDAAATDAKKEVSFSIGYAAGDPATKKAIAATVEAFMKANPNVKIKDISETTSSAYLDWLKTKDAVGEFPDLVEMRDTEVFADAGKIVELPSDLLELFKDPPQVNGKVWNAPMSVNVPQGIIYSKKAYADAGITGLPKTYDEFIAIQEKLKTSGITPIVVGGKDIFHMGFWVNKFLIDEVYTKDPDWNSKRTAKTVSFTDPNVVQAMTDFKDLFTNYVDKGWLSTGDNQTASILVSGKAAQLFSGTWMFSQIQEADPNFEFGFYAVPDREGKVNVIGLPSPAGWSLSAEAAKDADKTQAIKDFIRFFFAPEQYASYLASINAIPSTKENVTYETGEQMQTALDLIADPNVTKSLAINNWWGDNLIPPQFRNWYYKLLQDLVVKNGDVADYMKQADTEYDAQVKANAQ
>NZ_LN831776.1|WP_020431682.1|4605894_4607223_-|extracellular-solute-binding-protein
MQKKKWMRLQAVLLVLLAAILFLTACRDSGTGNSSVTAGGAGAHKEVHFSIAYAAGDPATKQAIAATIEAFMQAHPDIIIQDSSELSSSAYLDWLKIKDAVGEFPDLVEIRDTDAFASAGKIVELPSGLLELFGNLPQVNGKVWNAPLFVSAPQGIIYSKQAYARAGITRLPQTYGEFLDIQEKLKAGGMTPLVVGAKDIFHLGFWVNKFLIDEVYARDPDWNAKRTAKQVSFMDRNVVQAMTDFKELFLTDVNEGWLGTNDNQTASMLTSGNAAQLYSGTWMFSQIEEADPDFEYGFYALPDRRGKRNVVGLPSPTGWSLSAEAAKDTEKTEAIQEFIRFFFAPEPYSKFLASINGLPSTKEKVTYDTGEQMQEALKLMADPDVTKSLMINNWWGDNLIPPDFRNWFYKLLEEMILTDGDVSEYMKRADREYDRQVQDNQL
>NZ_LN831776.1|WP_052741494.1|4607322_4609071_-|sensor-histidine-kinase
MLIWGRRSKSIFVKFSASFLLVGLIPLLALSFFSVKTFSGYVERYTTSNLQQMVLYMSYNLNSAFNQYNEISKLMYTGRYEGFIDSYKQDQTANVNELEQINTIPIDSFLKTVLFSDPYISSAVFVRQSDGKLYSQEKENRSLDTNSFPAAEWLETMAPKPSAVAIFPTHTDQYFFRSNRKVFTIGRSLIDTSGKVTQAPKVVGTLFLDIDISLFEQFFRELSLGAKDELYLLDGEGHVYFSNQNLPEGAVAAAVQTNREMIGLSEDIPFLNGRVIARIHRGSLFEQLLSVRAAVYIAIMICAFVMVVMGAWFSRRLAAPIREIIRQMTVVESGRLDTRLSVNTNDEMGRLAHGFNRMVERLQIHIDEAYVAQIKQKQTELNALKSQIRPHYLYNTLEVIRMNAVDKEAGEVADMILALSNELKYVIDYGEDRASIRSELEHLQNYFYIISVRFENRYELVLDIAPEVQLDWPILKLSLQPIVENAVQHGLRQQGKGTVGITVEKKDRVLAVTIYDDGVGMSREALARITRTLEEPEAPSKNVGLKNVHERIRSTFGEAYGLSINSREHVGTSITLLFPVID
>NZ_LN831776.1|WP_046504227.1|4609106_4610705_-|response-regulator
MNRSIRVLLADDEPVILRGLKKLISWDTLGLDIVGEARDGIELKAMIDTCAPDLVISDISMPGFSGIDIIRDIHESGRPVKVVFISAYQEFSYARQAIQYGALDYIVKPVNTGQLEQVVGRAVAMIRQESEEERNKEMLKSYERKHHSITVEELLERLTDGNKGAASTLARMGNIAITRYASVCVLETDEYTGQTSRWEERERKLVEFALSNIIKETVETAGNGYVFRKGERFAVLLQHEQETEPEQIMLDLHHKINSYLKLQVSIGIGRPVSGMEEAGESYRSALKALKTRYFTGLNRVLRDQAGNQETTVAVSEWAAAQAALTEALKSLDKEQVPVLAARLLETVRLLSGDSRNQAVTHVYNSILQLEQELAGFGVDAGLVDPEDQPLLEKLADAPTFDALKQLFEGVLKRLAGQLTCKLNGKEMPQLLQVKAFVEEHYAENITLESMAALVYMNPYYFSSFFKKHTGQNFKNYVTETRMGHALRLLLQSDLMIYEIAERVGYNNARHFSDMFKKHFGKLPHEYKQTVKH
>NZ_LN831776.1|WP_020431678.1|4611014_4612775_-|glycoside-hydrolase-family-2
MTTKSYIPNYPRPQFVRNEWLDLDGEWNFSFDDANSGEAEAWYATFPEARKITVPFTYETAASGIGIPEFHPNVWYERTLELPAENAGKRAILHFQGVDYRAKCWVNGSYVGQHEGGYAAFSFDITPFVTFGAANRIVLKAEDSMDRTQPRGKQRWISDSFECFYVQTTGIWKSVWLECVSETRIDSVKMTPDVDRHMIRFDFRIAGLREGLELTLDTLISLKGRQVKRFSLGIDRDLVSLEVDVLHEAAGPWLQCLWSPEAPNLFDVEFTLLSGEESVDHVNSYFGMRKISIDNGQILLNNRPLYQRLILDQGYWTDSHLTPPDEQALIDDIDWIAEMGYNGLRKHMKIEDARFLYWCDVKGMLVWSEMAATYEFNDLAVERFTREWLEVVPQQYNHPCIITWVPFNESWGIPAIAKDVRQQKFTEGIYHLTKAIDPYRPVVTNDGWEHTVSDILTLHDYVEAGEQFLGTYADQNSIVNNGVSFNNYKFAWAEGYAYKGQPVIISEFGGIAFQTDSGWGYGNQVKTEQDFLERFQAITAAIKATPYISGYCYTQVSDVQQEVNGLLTEDRKPKVPLSKIREINLG
>NZ_LN831776.1|WP_020431677.1|4612832_4613639_-|carbohydrate-ABC-transporter-permease
MKWVYRLVSLFMAVLFAGPLVWMLFVSVKEEGMKIITVTDWFTPPYSFAVYQEILSGTKLTNWIGNSLLVAVFVTVLTVAAAALAGFALSKIPFRYRTLMFFVVLAGLLIPGEATIIPLYQVAKDMNLLNSYQGLIIPALASPVAVIVLKSFFDSIPNDLLESVQIDGGGSWRIFTRIMLPLCRPALASMAILTFIGSWNNFLWPFLSITDDNLFTLPMGIPTLISQYSEDYVKPMVVNAIASIPIIVLFVIFERQIVKGISMSGIKG

Crispr_ID: NZ_LN831776_47

• CRISPR_ID: NZ_LN831776_47
• CRISPR_location: 4775698-4775772
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_47

Consensus_repeat	Method
AAGTGGAAAAAGGGACACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_47

>47.1|4775721|29|NZ_LN831776|CRISPRCasFinder
TGCCGGAGTACCCTATCCTCGGGCAGATG

CRISPR arrays and Neighbor proteins around NZ_LN831776_47

CRISPR arrays

The CRISPR arrays of NZ_LN831776_47

>merge|NZ_LN831776|47|4775698-4775772|CRISPRCasFinder
AAGTGGAAAAAGGGACACTAATTTGCCGGAGTACCCTATCCTCGGGCAGATGAAGTGGAAAAAGGGACACTAATT

>NZ_LN831776|47|48|4775698-4775772|CRISPRCasFinder
AAGTGGAAAAAGGGACACTAATT	TGCCGGAGTACCCTATCCTCGGGCAGATG
AAGTGGAAAAAGGGACACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_081487167.1|4775274_4775577_+|YxcD-family-protein	unknown	unknown	gnl|CDD|313933
NZ_LN831776.1|WP_020432319.1|4769637_4769994_-|putative-DNA-binding-protein	unknown	unknown	gnl|CDD|234647
NZ_LN831776.1|WP_020432173.1|4781921_4782761_-|DegV-family-protein	unknown	unknown	gnl|CDD|273257
NZ_LN831776.1|WP_141639191.1|4778116_4778470_-|Asp23/Gls24-family-envelope-stress-response-protein	unknown	unknown	gnl|CDD|377129
NZ_LN831776.1|WP_020432321.1|4767368_4767599_-|KH-domain-containing-protein	unknown	unknown	gnl|CDD|224750
NZ_LN831776.1|WP_046504355.1|4774043_4774610_+|carbonic-anhydrase	unknown	unknown	gnl|CDD|239474
NZ_LN831776.1|WP_020427991.1|4772816_4773542_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020432171.1|4781043_4781748_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_LN831776.1|WP_020427989.1|4770367_4771015_-|hemolysin-III-family-protein	unknown	unknown	gnl|CDD|185044
NZ_LN831776.1|WP_039787707.1|4774859_4775288_+|membrane-protein	unknown	unknown	gnl|CDD|226830
NZ_LN831776.1|WP_020430738.1|4783897_4785649_-|hydantoinase-B/oxoprolinase-family-protein	unknown	unknown	gnl|CDD|376810
NZ_LN831776.1|WP_020432175.1|4782926_4783142_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046504358.1|4777691_4778036_-|hypothetical-protein	unknown	unknown	gnl|CDD|212474
NZ_LN831776.1|WP_052741498.1|4785632_4787153_-|hypothetical-protein	unknown	unknown	gnl|CDD|376810
NZ_LN831776.1|WP_020432167.1|4778503_4779610_-|AI-2E-family-transporter	unknown	unknown	gnl|CDD|223701
NZ_LN831776.1|WP_019910363.1|4767621_4767894_-|30S-ribosomal-protein-S16	unknown	unknown	gnl|CDD|234588
NZ_LN831776.1|WP_020432169.1|4779644_4781066_-|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_LN831776.1|WP_020427990.1|4771107_4772625_-|carboxypeptidase-M32	unknown	unknown	gnl|CDD|341054
NZ_LN831776.1|WP_020432320.1|4768230_4769616_-|signal-recognition-particle-protein	unknown	unknown	gnl|CDD|236780
NZ_LN831776.1|WP_020432156.1|4776587_4777541_-|LD-carboxypeptidase	unknown	unknown	gnl|CDD|132883

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_081487167.1|4775274_4775577_+|YxcD-family-protein	gnl|CDD|313933	pfam10850, DUF2653, Protein of unknown function (DUF2653). This family of proteins with unknown function appears to be restricted to Bacillus spp.	7.40799e-38
NZ_LN831776.1|WP_020432319.1|4769637_4769994_-|putative-DNA-binding-protein	gnl|CDD|234647	PRK00118, PRK00118, putative DNA-binding protein; Validated.	5.66674e-35
NZ_LN831776.1|WP_020432173.1|4781921_4782761_-|DegV-family-protein	gnl|CDD|273257	TIGR00762, DegV, EDD domain protein, DegV family. This family of proteins is related to DegV of Bacillus subtilis and includes paralogous sets in several species (B. subtilis, Deinococcus radiodurans, Mycoplasma pneumoniae) that are closer in percent identity to each than to most homologs from other species. This suggests both recent paralogy and diversity of function. DegV itself is encoded immediately downstream of DegU, a transcriptional regulator of degradation, but is itself uncharacterized. Crystallography suggested a lipid-binding site, while comparison of the crystal structure to dihydroxyacetone kinase and to a mannose transporter EIIA domain suggests a conserved domain, EDD, with phosphotransferase activity. [Unknown function, General].	5.83788e-90
NZ_LN831776.1|WP_141639191.1|4778116_4778470_-|Asp23/Gls24-family-envelope-stress-response-protein	gnl|CDD|377129	pfam03780, Asp23, Asp23 family, cell envelope-related function. The alkaline shock protein Asp23 was identified as an alkaline shock protein that was expressed in a sigmaB-dependent manner in Staphylococcus aureus. Following an alkaline shock Asp23 accumulates in the soluble protein fraction of the S. aureus cell. Asp23 is one of the most abundant proteins in the cytosolic protein fraction of stationary S. aureus cells, with a copy-number of >25000 per cell. A second Asp23-family protein, AmaP, which is encoded within the asp23-operon, is required to localize Asp23 to the cell membrane. The overall function for the family is thus a cell envelope-related one in Gram-positive bacteria.	1.51612e-25
NZ_LN831776.1|WP_020432321.1|4767368_4767599_-|KH-domain-containing-protein	gnl|CDD|224750	COG1837, COG1837, Predicted RNA-binding protein (contains KH domain) [General function prediction only].	8.93423e-25
NZ_LN831776.1|WP_046504355.1|4774043_4774610_+|carbonic-anhydrase	gnl|CDD|239474	cd03379, beta_CA_cladeD, Carbonic anhydrases (CA) are zinc-containing enzymes that catalyze the reversible hydration of carbon dioxide in a two-step mechanism in which the nucleophilic attack of a zinc-bound hydroxide ion on carbon dioxide is followed by the regeneration of an active site by ionization of the zinc-bound water molecule and removal of a proton from the active site. CAs are ubiquitous enzymes involved in fundamental processes like photosynthesis, respiration, pH homeostasis and ion transport. There are three evolutionarily distinct families of CAs (the alpha-, beta-, and gamma-CAs) which show no significant sequence identity or structural similarity. Within the beta-CA family there are four evolutionarily distinct clades (A through D). The beta-CAs are multimeric enzymes (forming dimers,tetramers,hexamers and octamers) which are present in higher plants, algae, fungi, archaea and prokaryotes.	3.52806e-58
NZ_LN831776.1|WP_020432169.1|4779644_4781066_-|HAMP-domain-containing-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	9.85725e-54
NZ_LN831776.1|WP_020432171.1|4781043_4781748_-|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	1.23423e-81
NZ_LN831776.1|WP_020427989.1|4770367_4771015_-|hemolysin-III-family-protein	gnl|CDD|185044	PRK15087, PRK15087, hemolysin; Provisional.	3.78189e-68
NZ_LN831776.1|WP_039787707.1|4774859_4775288_+|membrane-protein	gnl|CDD|226830	COG4395, COG4395, Uncharacterized protein conserved in bacteria [Function unknown].	2.63703e-06
NZ_LN831776.1|WP_020430738.1|4783897_4785649_-|hydantoinase-B/oxoprolinase-family-protein	gnl|CDD|376810	pfam02538, Hydantoinase_B, Hydantoinase B/oxoprolinase. This family includes N-methylhydaintoinase B which converts hydantoin to N-carbamyl-amino acids, and 5-oxoprolinase EC:3.5.2.9 which catalyzes the formation of L-glutamate from 5-oxo-L-proline. These enzymes are part of the oxoprolinase family and are related to pfam01968.	2.27392e-175
NZ_LN831776.1|WP_046504358.1|4777691_4778036_-|hypothetical-protein	gnl|CDD|212474	cd01727, LSm8, Like-Sm protein 8. The eukaryotic LSm proteins (LSm2-8 or LSm1-7) assemble into a hetero-heptameric ring around the 3'-terminus uridylation tag of the gamma-methyl triphosphate (gamma-m-P3) capped U6 snRNA. LSm2-8 form the core of the snRNP particle that, in turn, assembles with other components onto the pre-mRNA to form the spliceosome which is responsible for the excision of introns and the ligation of exons. LSm1-7 is involved in recognition of the 3' uridylation tag and recruitment of the decapping machinery. LSm657 is believed to be an assembly intermediate for both the LSm1-7 and LSm2-8 rings. Members of this family share a highly conserved Sm fold containing an N-terminal helix followed by a strongly bent five-stranded antiparallel beta-sheet.	0.00571786
NZ_LN831776.1|WP_052741498.1|4785632_4787153_-|hypothetical-protein	gnl|CDD|376810	pfam02538, Hydantoinase_B, Hydantoinase B/oxoprolinase. This family includes N-methylhydaintoinase B which converts hydantoin to N-carbamyl-amino acids, and 5-oxoprolinase EC:3.5.2.9 which catalyzes the formation of L-glutamate from 5-oxo-L-proline. These enzymes are part of the oxoprolinase family and are related to pfam01968.	1.10283e-71
NZ_LN831776.1|WP_020432167.1|4778503_4779610_-|AI-2E-family-transporter	gnl|CDD|223701	COG0628, yhhT, Predicted permease, member of the PurR regulon [General function prediction only].	3.43272e-50
NZ_LN831776.1|WP_019910363.1|4767621_4767894_-|30S-ribosomal-protein-S16	gnl|CDD|234588	PRK00040, rpsP, 30S ribosomal protein S16; Reviewed.	3.17024e-43
NZ_LN831776.1|WP_020427990.1|4771107_4772625_-|carboxypeptidase-M32	gnl|CDD|341054	cd06460, M32_Taq, Peptidase family M32, which includes thermostable carboxypeptidases TaqCP, PfuCP and FisCP. Peptidase family M32 is a subclass of metallocarboxypeptidases, distributed mainly in bacteria and archaea, whose members contain a HEXXH motif that participates in coordinating a divalent cation such as Zn2+ or Co2+. It includes the thermostable carboxypeptidases (E.C. 3.4.17.19) from Thermus aquaticus (TaqCP) and Pyrococcus furiosus (PfuCP), which have broad specificities toward a wide range of C-terminal substrates that include basic, aromatic, neutral and polar amino acids. These enzymes have a similar fold to the M3 peptidases such as neurolysin and the M2 angiotensin converting enzyme (ACE). The keratin-degrading extremophilic eubacterium Fervidobacterium islandicum M32 carboxypeptidase (FisCP) plays an important role in cellular metabolism, and significantly enhances the degradation of native chicken feathers. It has been shown to mainly cleave the C-termini of peptides with a basic amino acid sequence. Novel M32 peptidases from some eukaryotes: protozoa Trypanosoma cruzi, a causative agent of Chagas' disease, and Leishmania major, a parasite that causes leishmaniasis, have been identified, thus making these enzymes an attractive potential target for drug development against these organisms.	0
NZ_LN831776.1|WP_020432320.1|4768230_4769616_-|signal-recognition-particle-protein	gnl|CDD|236780	PRK10867, PRK10867, signal recognition particle protein; Provisional.	0
NZ_LN831776.1|WP_020432156.1|4776587_4777541_-|LD-carboxypeptidase	gnl|CDD|132883	cd07062, Peptidase_S66_mccF_like, Microcin C7 self-immunity protein determines resistance to exogenous microcin C7. Microcin C7 self-immunity protein (mccF): MccF, a homolog of the LD-carboxypeptidase family, mediates resistance against exogenously added microcin C7 (MccC7), a ribosomally-encoded peptide antibiotic that contains a phosphoramidate linkage to adenosine monophosphate at its C-terminus. The plasmid-encoded mccF gene is transcribed in the opposite direction to the other five genes (mccA-E) and is required for the full expression of immunity but not for production. The catalytic triad residues (Ser, His, Glu) of LD-carboxypeptidase are also conserved in MccF, strongly suggesting that MccF shares the hydrolytic activity with LD-carboxypeptidases. Substrates of MccF have not been deduced, but could likely be microcin C7 precursors. The possible role of MccF is to defend producer cells against exogenous microcin from re-entering after having been exported. It is suggested that MccF is involved in microcin degradation or sequestration in the periplasm.	1.78144e-102

Protein sequences

>NZ_LN831776.1|WP_081487167.1|4775274_4775577_+|YxcD-family-protein
MADTNMALTVLSMDEIINAICLHMAERKGVRVQEVQVELSWEEDTGYTAEVWVQGRSQYLVESNMIEAILRYLDGEYGIRAYREDVRLELDEEITAVVNT
>NZ_LN831776.1|WP_039787707.1|4774859_4775288_+|membrane-protein
MKRVMMILMAFTLFFAVTAPDFADARRGGGGFKSGTRGYTTTPKKSTTNNVKQSDSSTGTKAGTAAKANRGFFSGGSLMKGLMIGGIAGFLFGSMFAGMGAFGNLLGFAVNMLAIYLVVMLIMSFFRRRKERRRLQERDGRY
>NZ_LN831776.1|WP_046504355.1|4774043_4774610_+|carbonic-anhydrase
MSQITDILEFNKKFVEQKEYEAYLTSRFPDKKMLIITCMDTRLVELLPKAMNFKNGDVKIIKNAGAVISQPFGSVMRSVMVALYELDADEVIVVGHYECGMASLNADRMINSIKERGVSDEVLSTLENSGIKLTKWLRGFDNVEEGVIQTVELIKRHPLLPPNVPIHGMIIDPATGALELVSDGYAEN
>NZ_LN831776.1|WP_020427991.1|4772816_4773542_-|hypothetical-protein
MKKFVIGFVSGAVLFGGISAFAASGLVGQKVQSVVMIEKSGVKIADGAVINGAIYAPIQALAKATGTTVTIKDKKVTIGSPSASTANSTSSSSRSNPTDIGKTVNFNYKNGGYSGTVAVTQVLRGAEAWEAAKEQYNDFASEPDAGYEYLFAKIKVSILKVDKAGATADLNQFDYKLISTSGTEYGADIVLSPEPSISTKVYAGSSHEGWVGYKVKTDDASPLIAFSRNYDGTGGVWFKTK
>NZ_LN831776.1|WP_020427990.1|4771107_4772625_-|carboxypeptidase-M32
MEQLVKEEWEKFSGLLSKLSGYTEAIGLLHWDLRTGAPRKGVETRSNTIGLLSGEIFRLHTSTEMGEFTQFFSRPEVMNQLSDVQNKIVKDCRKEYERSQSIPAKSYEEYSVLTAHAQTIWEEAKESGDFNSFAPYLSKIVAFTQEFIDHWGVKDSRYDTLLDMYEPDLTVEKLDDIFGRLRSRLVPLVEAISASPNKPDKEFLAQVFPKEQQEKFGLFILGQMGFDFEAGRLDESVHPFATGLNPGDVRITTNYLPDNVTSAVFSSLHEGGHALYEQNISKELVGTPLAQGASMGIHESQSRLWENMIGRSRAFWHRYYGDLQQHFPEQLAGVGVEDFYRAINSVANSFIRIEADELTYNLHIIIRYEIEKLIFNEGLEVKDLPGVWNAKYQECLGITPPSNALGVLQDVHWSGGDFGYFASYSLGNMYAAQILNTLRQELPEFEDLIAAGNLLPIKDWLTEKIYRYGQSLTPSQIIEQVTGEPLNPDYLADYLEAKYTELYQL
>NZ_LN831776.1|WP_020427989.1|4770367_4771015_-|hemolysin-III-family-protein
MANTHTYSRKEEVANAVTHGIGVLLSIAALVLLVVFAAQNGTAWHVVSFSIYGATMLLLYINSTMVHSLKEGKAKDFFEFLDHSSIYLFIAGTYTPFMLVAIRGTLGWTLFGVAWGVAVFGVFFKAFFVKRFLFMSTIFYIAMGWMIVIAWNPLSAVLADGGMTLLLAGGLLYTLGTVFYVWRGFPYHHAIWHLFVLGGTVAHFFVVLLYVLPIH
>NZ_LN831776.1|WP_020432319.1|4769637_4769994_-|putative-DNA-binding-protein
MSQENRLEKTNRINLLFAFYERLLTDKQQTFLKYYFHDDFSLGEIAAEFEISRQAVYEHIKRAEQVLENYEEKLGLLEKHESRSKYLEELRRLPENGMLPEQYTLRFTELVDRLQRLE
>NZ_LN831776.1|WP_020432320.1|4768230_4769616_-|signal-recognition-particle-protein
MAFEGLTGRLQNVFSKLRGKGKVSEDDVNEAMREVRLALLEADVNFKVVKEFVSKVKEKSIGKEVMDSFTPGMVIIDIVNKELTELMGGSQAKLAKSNKPPTVIMMAGLQGAGKTTTSGKLAKLLQKGNHRPLLVAGDIYRPAAIKQLQILGEQIKVPVFTLGDQTSPVEIARQAVQHAKDNNLDYVIIDTAGRLHIDEELMEELKQIHTVTNPDEVLLVVDAMTGQDAVNVADSFNKQLELTGVVLTKLDGDTRGGAALSVKAVTGCPIKFAALGEKIDALEPFHPERMASRILGMGDMLSLIEKAQANIDTEKAKEMERKMRNAEFTFDDFLEQMDQVKKLGPIDQILDMLPGMNKAKGMKDLKVDDKQMGRVEAIVHSMTKAEKAQPEIINHNRRKRIAAGSGTNVAEVNRLIKQFDEMRKMMKQFSGMMGGGGKGGKKNAMKQLKGLGGKGMKFPFR
>NZ_LN831776.1|WP_019910363.1|4767621_4767894_-|30S-ribosomal-protein-S16
MAVRIRLKRMGAHKAPFYRVVVSDSRSPRDGRFIEEIGYYNPIEVPAVVKIDEEKALKWLQTGAQASDTVRNLLSKAGVMKKFHELKQQK
>NZ_LN831776.1|WP_020432321.1|4767368_4767599_-|KH-domain-containing-protein
MEELVGVIAKALVDHPEDVAVRTVEKDHLIVYELSVHPDDVGKVIGKQGRIAKALRTVVTSAAVKSDKRVTVDILS
>NZ_LN831776.1|WP_020432156.1|4776587_4777541_-|LD-carboxypeptidase
MITYPVIKKGAAIGVTAASAGVGPQSVELFGQAITRMEEKGYHVLCGDTVFRHDKAKSASGLVRGKEFNQMMSSDEVDLILPPWGGELLIEMLEHIDFSQVKNKWIMGFSDISLLLLVITLRTGIATAHGPSLGDLRGEVIDKTTAKWETVLSTASGESVIQRSSPTDWKTVSGEAVTLQGRLLGGCIDVIRHIIGTPYGDVRHFQENFIHQEPILWYLENCELNTADLRRSLVQMKLAGWFDNCSGVMFGRSGSNTPMENYTAEDVYRELTEELQVPVVYDLDYGHIPPQMTLINGAYAEVKVSGGAGTITQYFYE
>NZ_LN831776.1|WP_046504358.1|4777691_4778036_-|hypothetical-protein
MSFYQSGQPATVIYQADPAVVQHLHGVRESLHHSCMPYLNHKVSVKTIDGQVHEGTIAGMDNKHMYLMVECPTDMGRGYYNPYYNPYPYPYPYPYPNNAILPLVLFELLAIFLI
>NZ_LN831776.1|WP_141639191.1|4778116_4778470_-|Asp23/Gls24-family-envelope-stress-response-protein
MGMEQDSHKGLVNISDRVISAIIGYAVMDTPGIAGMSGSTVTGNLAKRLGGKISKKGLSVEVTEEDVAIHLQVIINYGYAIQEVCKSVQQNVRSAVENMLGLTLGVVNIRVEKLALP
>NZ_LN831776.1|WP_020432167.1|4778503_4779610_-|AI-2E-family-transporter
MAKLNLFIRICIAVLLVLGIIYLGTQVKFIFTPVLSLFRVVIVPLMLAVFFFYLLRPLINWLESRKLNRTAAILLVYLSIAVLLLAFSVGVWPSLKSQLVNLGNNMPNVFNALGEQLTKLEDSKLLSSLIPADMNPAGQLMNYLNKGFSLLSNSMSELFSFVSNFAVVLFTFPILLFYMLKEGGKFGVKVVSFFPKRFHKEGEGVVADIDEAMSNFIVGRVLVNLALGVLMYLGFLLIGLPYALLLTVVAVLMNFIPFIGAILSTVPIFIIGLMESPSTAIWSIVVVLVAQQIQDNLVAPYIFGKSLDIHPLTTIILVLAGGDFGGIIGILLIIPVYMMLKIITVKLHQLYMRQRWPEEPQLSADAVD
>NZ_LN831776.1|WP_020432169.1|4779644_4781066_-|HAMP-domain-containing-histidine-kinase
MKHPWKSRDNRPLQTSLTLDFLLFNCMLLLLVLGVYLFIQKDITHMILDKRLTDPNLPVEAGQYLEELGEGPRSAQLLHSGGWLELLDSNKQVIRVVGDKEDQIRSYDEDRLFLGLENRKDQPYYYSIAKIEGDGQAAWLLLKIPRDVIKVSIDNELLVSYLNHSVFFYVFLVSGLILLLIFVYSYWVTRRIKKPLRVLNLGLKQMMEGHYSTRIALYAETEFLRIGESFNYMADVIEKTTEEKRRAEKSKQRLMVDLSHDLKTPITSIQGYAQALMEGRGTDPERQTKYLNYIYSKSVQVTKLIQHMLELLKLDSPDFILRTERLELGDHLREIVADTYGEIEQKDFQLQLQVPEEEMYAHYDPELFASVVNNLISNALAYNPNGTHLRVSVFPEDTEIRIEIADNGVGIPKELWSTIFDPFVRGDEARSTASGGTGLGLSIAKKNAEKMGGSLELASREGEPTVFTIRVPK
>NZ_LN831776.1|WP_020432171.1|4781043_4781748_-|response-regulator-transcription-factor
MYTILIADDELEIVELLQLYLEKEYNILQAQNGNEALKLMQSHTVDLAILDIMMPGMDGLQLLKRIRENDHFPVLFLSAKSQYHDKILGLELGADDYISKPFNPLEIVARVGSMLRRVHEFDAPAVQEKKKEQIVLGRLLLDRSSCQVEVDGEPVALTSTEYKILELLMEQPGRVFTRKKIYEAVWEDFYVYEDNSIMVHISNIRDKIERDSKKPEYLKTIRGLGYKIEAPVEK
>NZ_LN831776.1|WP_020432173.1|4781921_4782761_-|DegV-family-protein
MPIKIITDSGSDLPLEYAEKYNVDIVHLPVHFGHELMPEDADTQAFYAKMRESKELPKTASPSPQVFLNKFKQVEPGTDIMVVCMSSNISSTYQAAVIAKDLYEEEGHSNAIEIIDSKNFSGGLSLIVAFTAKWSLTCSSLAELKQMVLDKIGEVNAYFTLDTLENVIKGGRLNRLSGAVASVLNIKLLLKISDEGTVEVVEKTRGLPKALSHLLAKLEHKQHDYEKAVIAIVHSNCEKLAQEIKERILEKHPFKEILFSSMGPVMGTYAGEGGIGVAF
>NZ_LN831776.1|WP_020432175.1|4782926_4783142_+|hypothetical-protein
MSKGRVWNKGKHNGRGLSKKNIAAEVTDNKSQPAPAPEESFIPRIDTVKPMNRSNWVTRPARVVPKEPENK
>NZ_LN831776.1|WP_020430738.1|4783897_4785649_-|hydantoinase-B/oxoprolinase-family-protein
MARKVDDWLLSQIVGGTLDSVAEEMSAVVTRTARSPIFNEAHDFTTGVFDFTRSSTRLVAQAPGCTLHLYAIVSAVDQLMEAFKNDLHPGDVLLVNDPYHGGSHSLDWTIVMPVFHGRRPILLPAVRSHMGDNGGPVAGGYNPRSRDIWHDGLRIPPIKLYARGEKRRDVFEMILANNRLEHWLEGDLDAMIGACKMAAERIGQLLERYGPPSVIGAIEQRIEYTERRVREEISSWPDGTYTAETFADHDFQGNRDIKIRATVKVEGSGLEIDFTGSSPQVAGFINSPLSNTTSFAFVAVSTCCDESIPINEGYMNPVKVTAPEGTVVNPRLPAPCGHATACVGAEIAEAVLLAISQCAPERAGVNAHKLPLAYTNGTYEDGRPWVNLNFFGYTGGAGGAFETDGWGLYPPVMTGVILPSIEMNELQYPSRVLKHEYAADYTGAGQYRGAPGLEVKIQHLEPSYTSVMMAGVRNTTRGLCGGGDAPANLVVLGDGQSAPLEVRETAFHVHMEPGGIITFHRAGGGGWGNPLLREPGKVLEDVLNGIVSVEGAEREYGVGIVRVDGGFAVDDRKTAELRQLKQG
>NZ_LN831776.1|WP_052741498.1|4785632_4787153_-|hypothetical-protein
MPPVHSIEDQIIYGKIAAVSRHAGEQLQRISRSPLIAESRAFAAGIVTEAAGLVHQIQGEAEHLYALRASTRAMYDHFAYDLEEGDVLISADVYKGGTKGQMLTMVLPFFLEGELTLSPVIRVQLTDLAGEYPGGYHPEAFEMWQESMRITPVKLYSGGKLQRDVQRFVLANSRTPGLLASDLDALRASLLQAQTGLRSIIQAYGLSKVARAIGQMKAHTQEQVLNLLPEGRKEWCGAADFSASKVSGRVQVRMQREGNLWKADFTGSASQVEAPFNCSEATTSACAVVAILAEHLESLPVNDGLLDVFDFKLPAGSIVNPAYPSATALGYHTAGQAVAAAVTHALNGSDNNEGKFPAVHGAAPLTVLYSPIGSQKQTVPVFLELGYTASAGGWGPPVLHSGRSLASAEELEWRSGLRMTQRELAGDEGMEVRVELLDGSWEACIFVPDQADSSGLSVAVESCGEVWKGTVTGLPISAGATIHYTFARNGGGRPAEKEVGLHGKKG

Crispr_ID: NZ_LN831776_48

• CRISPR_ID: NZ_LN831776_48
• CRISPR_location: 4912651-4912736
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_48

Consensus_repeat	Method
GATCATCTGATGTTGCACTATGTCTGATCT	CRISPRCasFinder

spacers of NZ_LN831776_48

>48.1|4912681|26|NZ_LN831776|CRISPRCasFinder
ATAAAAGATTAAGATCAAAACACCTC

CRISPR arrays and Neighbor proteins around NZ_LN831776_48

CRISPR arrays

The CRISPR arrays of NZ_LN831776_48

>merge|NZ_LN831776|48|4912651-4912736|CRISPRCasFinder
GATCATCTGATGTTGCACTATGTCTGATCTATAAAAGATTAAGATCAAAACACCTCGATCCTCTGATGTTGCACTATGTCTGATCT

>NZ_LN831776|48|49|4912651-4912736|CRISPRCasFinder
GATCATCTGATGTTGCACTATGTCTGATCT	ATAAAAGATTAAGATCAAAACACCTC
GATCCTCTGATGTTGCACTATGTCTGATCT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020433665.1|4911670_4912423_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224059
NZ_LN831776.1|WP_020433670.1|4914665_4915004_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020433674.1|4917291_4918623_+|hypothetical-protein	unknown	unknown	gnl|CDD|176469
NZ_LN831776.1|WP_141639231.1|4918682_4919594_-|hypothetical-protein	unknown	unknown	gnl|CDD|237468
NZ_LN831776.1|WP_046504490.1|4898177_4898981_-|undecaprenyl-diphosphate-phosphatase	unknown	unknown	gnl|CDD|234712
NZ_LN831776.1|WP_020433667.1|4912816_4913821_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|340424
NZ_LN831776.1|WP_020433669.1|4913817_4914507_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_LN831776.1|WP_020433659.1|4903394_4904402_-|zinc-binding-alcohol-dehydrogenase	unknown	unknown	gnl|CDD|176217
NZ_LN831776.1|WP_082118130.1|4905285_4906245_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_LN831776.1|WP_039791001.1|4906283_4907870_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270301
NZ_LN831776.1|WP_020433680.1|4922042_4922633_-|isochorismatase-family-protein	unknown	unknown	gnl|CDD|183137
NZ_LN831776.1|WP_020433679.1|4921087_4921852_-|glucose-1-dehydrogenase	unknown	unknown	gnl|CDD|235816
NZ_LN831776.1|WP_046504501.1|4915195_4917070_+|LTA-synthase-family-protein	unknown	unknown	gnl|CDD|224287
NZ_LN831776.1|WP_020433664.1|4909736_4911674_-|ABC-transporter-permease	unknown	unknown	unknown
NZ_LN831776.1|WP_020433660.1|4904428_4905292_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_167345647.1|4919715_4920156_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020433663.1|4908151_4909522_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_LN831776.1|WP_020433654.1|4897347_4898199_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_167345648.1|4920214_4920793_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020433656.1|4899239_4900049_+|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|379312

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020433665.1|4911670_4912423_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224059	COG1136, SalX, ABC-type antimicrobial peptide transport system, ATPase component [Defense mechanisms].	2.55888e-107
NZ_LN831776.1|WP_020433674.1|4917291_4918623_+|hypothetical-protein	gnl|CDD|176469	cd01597, pCLME, prokaryotic 3-carboxy-cis,cis-muconate cycloisomerase (CMLE)_like. This subgroup contains pCLME and related proteins, and belongs to the Lyase class I family. Members of this family for the most part catalyze similar beta-elimination reactions in which a C-N or C-O bond is cleaved with the release of fumarate as one of the products. These proteins are active as tetramers. The four active sites of the homotetrameric enzyme are each formed by residues from three different subunits. CMLE catalyzes the cyclization of 3-carboxy-cis,cis-muconate (3CM) to 4-carboxy-muconolactone in the beta-ketoadipate pathway. This pathway is responsible for the catabolism of a variety of aromatic compounds into intermediates of the citric cycle in prokaryotic and eukaryotic micro-organisms.	0.00237209
NZ_LN831776.1|WP_141639231.1|4918682_4919594_-|hypothetical-protein	gnl|CDD|237468	PRK13684, PRK13684, photosynthesis system II assembly factor Ycf48.	1.0889e-08
NZ_LN831776.1|WP_046504490.1|4898177_4898981_-|undecaprenyl-diphosphate-phosphatase	gnl|CDD|234712	PRK00281, PRK00281, undecaprenyl-diphosphate phosphatase.	1.47568e-97
NZ_LN831776.1|WP_020433667.1|4912816_4913821_-|sensor-histidine-kinase	gnl|CDD|340424	cd16948, HATPase_BceS-YxdK-YvcQ-like, Histidine kinase-like ATPase domain of two-component sensor histidine kinases similar to Bacillus subtilis BceS, YxdK, and Bacillus thuringiensis YvcQ. This family includes the histidine kinase-like ATPase (HATPase) domains of various two-component sensor histidine kinase (HKs) such as Bacillus subtilis BceS and Bacillus thuringiensis YvcQ, the HKs of the two-component regulatory system (TCSs) BceS-BceR and YvcQ-YvcP, repsectively, which are both involved in regulating bacitracin resistance. It also includes the HATPase domain of YxdK, the HK of YxdK-YxdJ TCS involved in sensing antimicrobial compounds.	3.10867e-47
NZ_LN831776.1|WP_020433659.1|4903394_4904402_-|zinc-binding-alcohol-dehydrogenase	gnl|CDD|176217	cd08255, 2-desacetyl-2-hydroxyethyl_bacteriochlorophyllide_like, 2-desacetyl-2-hydroxyethyl bacteriochlorophyllide and other MDR family members. This subgroup of the medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family has members identified as 2-desacetyl-2-hydroxyethyl bacteriochlorophyllide A dehydrogenase and alcohol dehydrogenases. The medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family, which contains the zinc-dependent alcohol dehydrogenase (ADH-Zn) and related proteins, is a diverse group of proteins related to the first identified member, class I mammalian ADH. MDRs display a broad range of activities and are distinguished from the smaller short chain dehydrogenases (~ 250 amino acids vs. the ~ 350 amino acids of the MDR). The MDR proteins have 2 domains: a C-terminal NAD(P) binding-Rossmann fold domain of a beta-alpha form and an N-terminal catalytic domain with distant homology to GroES. The MDR group contains a host of activities, including the founding alcohol dehydrogenase (ADH), quinone reductase, sorbitol dehydrogenase, formaldehyde dehydrogenase, butanediol DH, ketose reductase, cinnamyl reductase, and numerous others. The zinc-dependent alcohol dehydrogenases (ADHs) catalyze the NAD(P)(H)-dependent interconversion of alcohols to aldehydes or ketones. Active site zinc has a catalytic role, while structural zinc aids in stability.	1.16575e-73
NZ_LN831776.1|WP_082118130.1|4905285_4906245_-|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	1.24992e-132
NZ_LN831776.1|WP_020433680.1|4922042_4922633_-|isochorismatase-family-protein	gnl|CDD|183137	PRK11440, PRK11440, putative hydrolase; Provisional.	6.61021e-65
NZ_LN831776.1|WP_020433679.1|4921087_4921852_-|glucose-1-dehydrogenase	gnl|CDD|235816	PRK06500, PRK06500, SDR family oxidoreductase.	1.80587e-82
NZ_LN831776.1|WP_046504501.1|4915195_4917070_+|LTA-synthase-family-protein	gnl|CDD|224287	COG1368, MdoB, Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily [Cell envelope biogenesis, outer membrane].	9.937e-102
NZ_LN831776.1|WP_039791001.1|4906283_4907870_-|extracellular-solute-binding-protein	gnl|CDD|270301	cd13583, PBP2_AlgQ_like_4, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	3.06002e-110
NZ_LN831776.1|WP_020433660.1|4904428_4905292_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	4.80027e-66
NZ_LN831776.1|WP_020433663.1|4908151_4909522_-|extracellular-solute-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.18447e-31
NZ_LN831776.1|WP_020433669.1|4913817_4914507_-|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	1.62349e-60
NZ_LN831776.1|WP_020433656.1|4899239_4900049_+|class-I-SAM-dependent-methyltransferase	gnl|CDD|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	3.81647e-18

Protein sequences

>NZ_LN831776.1|WP_020433665.1|4911670_4912423_-|ABC-transporter-ATP-binding-protein
MILEANKIYKTYGNKFNRQEVLKGIDLQVSKGEFVGIMGASGSGKTTLLNVLSSIDRVSQGTIEIEGKEFTRMKEKQLAEFRKQHLGFIFQEYNLLDTLTVKENVLLPLSITGISRREAHQKFEQVAGELGIYELKDKYPAEISGGQKQRTSAARAFIHDPSIIFADEPTGALDSKSASDLLNKLADMNTKRQATIVMVTHDAIAASYCSRVVFIRDGQIYTQLNKGDEARQSFFNDIMKTQSVLGGVQQ
>NZ_LN831776.1|WP_020433664.1|4909736_4911674_-|ABC-transporter-permease
MSINYIILLNLRKNIKNYYLYVFALVFGVALYFSFVTLKYDPSLDIVAGSIKGGAALGASSVLLVAIVAIFLLYANTIFIKRRSREIGLFQLIGLTKGKIFKLLSAENLILYFGSMLLGIGAGFAVSRLILMILFKILAIESVAKLRFSMEALQQTVIVFAGIYLLIMLMNYTFIKAQSILSLFKVSSTAQERIRKMPLWEIVLGLLGIGCIASGYYLSTLLFSGKLDDMTRLMTSMIVILGLVIIGTYLFYKGTVSFVFNAIRKSKQGYLTINEVLSLSSIMFRMKSNALLLTIITTVSALAIGLLSLSYIAYYSAGATAKDNSPDDFGFAQVEAKERFVQALDKAHIKYSEVHMQPIPMEVDGSQIMEQGSRNTVISTLVVSDSSVEGVDLKPGEARIMGYYNNVLSSYMTLKESGGVGFKTMNGTIEQQLTGISGKTIMPYFYSKGAGVFVVDETVYEELAQGQDPKLRSAKGAAAADYFGIELADRSQLKDANQIFTDQKPGEMSISQYEYKMNHRSGMGLIMFIVGFLGLTFLITSGCILYFKQMDEGEEEKAGYTILRKLGFTQGDLLRGIQFKQLFNFGIPLVVGLSHSYFAVKSGWFFFGTEMLTPMIMVMLLYTVLYSVFGFLSVLYYKRVISESL
>NZ_LN831776.1|WP_020433663.1|4908151_4909522_-|extracellular-solute-binding-protein
MAKIDRHTFQTKTRHMSADLKQKINSGAYSPGEYLPSELALTELYKLSKNSVRYVLDELVQEGLIIKIPRVGTQVAKSIAKETIRFGVYPSLYKEAGMEELIRRFHETHPHIHVETIELPYVSSDSIANLIKLGIVDVLTVNLQDMYQFKERNSLDLFAGQDRHDNIYPFLTTYFEKEPGVVAAQPFVYSPVILCYNKEHLKEKRLGEPNSSWSWDELATLLRELKAPHRYSIAFQLFSMNRWPIFWMQNEDDPASADYNPSQDGTSLPTEGLRWLRDLVTEEGIFPLALAQGEFEAEKLFREQKVSVMLTTYYMLNELKNADFSFDIAQLPHFKNDKTLLLSTGIALSAESGHKEPAACFVNYLTSDEAQTYIRQHTYSLPASRYITETVSVDMINKPSRLELHRDYSSKYTTYHDLSMSIETLIRFGESLKQYMSYLTDEEGLAEVLLPAKSLN
>NZ_LN831776.1|WP_039791001.1|4906283_4907870_-|extracellular-solute-binding-protein
MLKKRISIMLAATLFSSILAACGSSTDKSGSAALPSQEPGQYGDTGTLTLPLVDKPTTITYMLPSNAKDLGPGKLVVQELEKRTGIKVDFQTYSPQTYQDKLKVIVASGKLPDIFTGLKPAELKKIGKQNGVVAINKYADQLPNFKKLYMEENDWVLKSFGDEAGDIYTWPIYNLNRKVNHGFMFRKDIFDELGIKEWTNTDEFYEALKKVKAAYPDSYPYASKSLANIFRDWAFGWGLGNTDQYPAYYDEKDGTWKYAAVQQAHKDMLDFMKKLYNEKLLDPEFLTDTQDSWTTKMTTDKSFVTFDWIGRLDLFYNQIKEQNPDYDLRYANPVGPTGNVRTLPEVSDFSVAVAKNKNTEASLKLLDYLTSPSGSELMTIGVEGVNFEWGEDGFPVYPELKDLPLVDITVLEDRYAMWLEGAYLRPDHRSIYYRFSEKEQEAQDKIVKEDRFEPLDPILNFTDEETSKIAELQTSLQKSAEEFNAKYILDAGYGEAQWADFQTKLSRSGVEELMSIYNEAQKRYDESK
>NZ_LN831776.1|WP_082118130.1|4905285_4906245_-|sugar-ABC-transporter-permease
MEHPAANQTMHKKSSRSRLGTTWNHIKRDRQLLLLFLPCILFYVVFRYGPLYGLIIAFKDYSVFSGVLGSEWVGFEHFITFFTNHDFWMLFRNTLLLGLYTLIFGFPFPIMLALLLNEVRNKWLKKSVQTFSYFPAFLSVVIISSMIIDFLSPNHGILNQMLAAFGFEKKYFLVDPGWFRPIYVISEIWANMGYESIIYLAAIAGISPTLYEAAKVDGASRFHMIRHITLPGLFPTMLIMFILKTGSMIRVGYEKVLLLYNPMTYDVADVFSTYVYRKGLLESNYSYAAAVGLFEALVAMVMLLSANAVSKRLGGNGLW
>NZ_LN831776.1|WP_020433660.1|4904428_4905292_-|carbohydrate-ABC-transporter-permease
MVGERKISWFGVINTLILTLVAVATLYPIVYITAISLSDTVSVVQGKVFLFPKGFNFEAYGEVLKNDTIPRAYLNSVFYTALGTFLNLLFTAVAAYPLSQKGFFGRKFFMTAIVLTMFLNPGIIPTYVVVQQLGLTDSVWALVLPNAIWTMELIILKSFYENMSSQIREAALIDGASEYRILFNIVIPLSKPALASIGLFYFMGHWNSFFLPLIYLNDADKYPLQVVLRDMLIYSAENDAGLVDRSALAPQSIKNATIVLSMIPVLLIYPFAQKYFAKGVMLGSEKG
>NZ_LN831776.1|WP_020433659.1|4903394_4904402_-|zinc-binding-alcohol-dehydrogenase
MRIVAAKEGKVAILQAAIPELNKRHVQVRTEYSGISPGTELSSIKRSGLSPVSLGYSAVGIVEQTGSEVRDIHPGDRVACYGVPYVRHAEVISVPTNLVTKVPHHVNPEEAAFTGLGAIAIHALRTADVRFGDKVLVVGLGILGNLVAQIASAAACHTAAYDLSEDRVQLLQGQMGITSGFSSEEEVEHFVMNETGGAGFDSILLCAGGPGEVLINKSLEWLRDLGKIVIVGDLSMEFSRDLMFRKEAQILISRAGGPGRYDMRYEEDNQDYPIGFVRWTEGRNMDEYVRLLAEKRITVSPAITHRFALEEAPAAYGIYQSGPAQGALATLIKYV
>NZ_LN831776.1|WP_020433656.1|4899239_4900049_+|class-I-SAM-dependent-methyltransferase
MDNNTVRTNIIGAGEVGRAISADMDKNAIHKTNSSFWDTKGTEILGATALPLYGAFVSEEQCRLFGDIAGKKLLEIGCGSGQSLQYMGERKAAELWGTDISEKQIEKTGQLLKSCGLSATLICSPMEEECGIPEDYFDFVYSVYAIGWTTDLEATFGRIASYLKKDGIFIFSWSHPIHKCVGAENNMLVFKKSYFDESWYSVSLEESTLTLSDRKLSTYVNALSKAGFVIEQMVEESDEEIMQSRNDNSDFAKKAKMLPVTFVFKARKL
>NZ_LN831776.1|WP_046504490.1|4898177_4898981_-|undecaprenyl-diphosphate-phosphatase
MTDVIKAIILGIIEGLTEFLPVSSTGHLILAGDLLSFEGDAAITFKIVIQLGAVMAVLILYWRRYLAIGANLIRMDFSKSKGLNVIHMILAMLPALILYLLFKDIIKSRLFGPTPVLIGLVAGGLLMILAARSRKTNTADTIDGINYKQAFGIGLFQCLALWPGFSRSGSTISGGLLLGTSQKAAADFTFLISVPVMFGASLLDLYDSRDLLNSDDLILMLIGFTTSFLVAMIAVVTFIKLIKRLRLEWFALYRFALAALFYLIVIL
>NZ_LN831776.1|WP_020433654.1|4897347_4898199_+|hypothetical-protein
MILILVILVGITVGVMIFFHIPYSRTKAEFLRLADNGLSAAAASNDVFTSEDWKALPSPVQKYFETSGWTGTPKMSSMKAVFKGVDFILSPKKPAIQIDYTQYNFSQRPARIALIETSMYGIPFQGLDTYVEGKGSMKGVLAKLFTLFNQQGREMDQACLVTFLSESLLLPSAAIQSCITWEPIDDTHARAVIACYGITAGGIFSFNDNGECLSFTTDDRTAVGMDGSKQRVRWSALMKDYKQIDGVRQPTRLQAVWHYDSGDLVYFDSRNFRVEYSYRMTIK
>NZ_LN831776.1|WP_020433667.1|4912816_4913821_-|sensor-histidine-kinase
MIRKYIKEKLSWLLLLGGLQIIFLFVAYVDSSIPFLSVLYIVVLNIMVCTTFVFLRYHKETRFYQRMGAWDEVYDLSTFKEANSPFERMVQEAVNAQTERYRRESSANFQLLEQEKDDLLSWIHEVKTPLTAMQLMIERLTDETLKPKLMYEWLRVHHLLDQQLHQKRIPFMRNDLYIEMIRLEPVLNKEIQALKSWCIPKGIGFDVDLAVEAVLTDGKWLGFILRQLLTNAVKYSENSDILIQSREKAGHTVLIIEDHGRGIDPKDLPRIYDKGFTSTTGRQEGAATGMGLYLTKQVAEPLQIGIHADSMLGEGTTFTLTFPRKNDFLRITGM
>NZ_LN831776.1|WP_020433669.1|4913817_4914507_-|response-regulator-transcription-factor
MFKIMLIEDDVTLFGEIKERLSQWSYEVYGISDFGKVLQEFTAAKPELVIVDIQLPQFDGFHWCRILRAHSNVPIIVLSSRDHPSDMVMSMQFGADDFIQKPFHFEVLIAKIQATLRRVYNYSTERTELKTWRGATIEYVKNTITLEHESALLTKNEMLILKILVESKDRIVEREELIRKLWDNEHFVSDNTLTVNVNRLRKKLEPLGLDAYIETKVGQGYMATEEALV
>NZ_LN831776.1|WP_020433670.1|4914665_4915004_-|hypothetical-protein
MKIKGLEGLTWETLEQEVGQGGKFVVYTFCISILIMTFWRSSSIYYIAPGMGAVGTGLKFTVFSVLFGWWGIPWGPIYTIGALITNFKGGRDMTVEVLNSLAEQRGPQQQIG
>NZ_LN831776.1|WP_046504501.1|4915195_4917070_+|LTA-synthase-family-protein
MRLKEPRTLSKRSILFFSLIMLAKSYFAWYYLFEDGPTWTTWLKEIPFILLIFCLIEWFATKRKIAIYMIVNLLITVLFFSLIVYHNHFGIIATSQVIGQAKQVGAVKKSIFSVLHPQYMLIFLDIIIISLVMFSRKKAVAWKKAMSRRSNRKAVAALFCISLIICMMNIFPNQASMNETVQAEQMGILNYEAYALLAEHKEEQIELSQITQAAIDQKKGIQEQSNPALFGAAKGKNLIIIQMESFQNFLINLSIDGQEITPNMNKLAAGNFYFPRFYQQVGQGNTSDAEFIVNTSFYVPPDGPATDIYAPKELPSLPKLLQAQGYDTATFHTNEVDFWNRGELYKALGFDRYYDKAFFGEDDKVFYGASDEILYKKTSAELARMDQRSQPFYSHVISMSSHNPFTIPEDKYKMALPERFEGTLVGNYIRAQNYADYALGQFIDELKQNGVWDNSLIMLYGDHRGLPIFSLKEEDHVLLEEILNHKYTERDLINIPLIIASPGLTTPSVKEQLGGQVDILPTVSNLLGVSLDSHIHFGQDLLNQSAYNLLPQRYYLPTGSFVNNEELFLSGSGFKDGQHYTLSGDGMKPLQATEDEFNRALELLHLSDSYVTQLPDREVKGEEN
>NZ_LN831776.1|WP_020433674.1|4917291_4918623_+|hypothetical-protein
MRKSISVISTLAVTMLFSSQLAFAEEAVLPANNILPQTESQEIAQKADIKVIDLLDQSNSVDTGQKAIPSQQAASLLPPQLQAASNYNFSPRDFGYSIVQTSDGGYVYTGSTTVNGNEDIIFAKTDAALTLQWAYAYGGTGAESGAEVRATSDGGYMIAGTSNASGSSDVILVKTDASGTVQWSKTYGGPVKEEAQAMELGTDGGYIVVGTKESSSNSNDAYMLKVDANGNIQWTRTFGKDNLEDRFYGVAVTPDGGYVAVGYKTLSEIINPGTAQRMYGLMVKVNGSGNTVFESTLDRYSMLNGVAATSSGYVAAGSINNVDLPNNSQLYNIFVTKVSTSGSQSWSRQFHATNGDFANDIKLAKDGNFIVTGFITPAVYKEDLLMLKIDGSGNTQWSNTYSFGDTGEIGRSVAAASDGGYVVTGSYLANNDYDVLLLKFGSD
>NZ_LN831776.1|WP_141639231.1|4918682_4919594_-|hypothetical-protein
MMWKGLLLKTHWIAAVVLMALAGIWGSGISEGSGSKIKPGTVYTRNSAGEQVIAYNAGHLYTLDKDGHVMISYNNGKTKVKAPLTLNPGYDEESGMTADGSGFFISTDKTAIVYGGSRAIPVQVLITNDQGKTWNTYPVTKEVTGTTKNIGFINKNDGWMILSSFKGMGSEDHYLYKTRDGGKTWNEVKGNANEVYARVLTGAGFANDKIGFMGFRYETDFQPAVCWTQDGGKSWTKLHLKLPGGFEEYSLTPLSPVFDGARGQFPVQLSKDGASNVVGTIYLTSSNYGKTWKYQKLVRNLNP
>NZ_LN831776.1|WP_167345647.1|4919715_4920156_-|hypothetical-protein
MSLLVPLLILLPNLLFFQLEPQNMPDKTTRNRFFTGAEFIGRMGVIIVPLFYSLHMQNGLEVLALIVMLLSLGIYYYGWGRYFRNGRPYRLLFTPLMGIPVPLALSPVLYFLSASVILHSGYLLIFSLILGAGHIPASLSDYRRNV
>NZ_LN831776.1|WP_167345648.1|4920214_4920793_-|hypothetical-protein
MTSEQAGKLITANINETSSRNGTAHWTDITPPDIWEQTGHQLFKNIEETSSWDTFAVSDGKAVQIGIGFGGYGVTSAVPYDVNKDGTADIVYAYSFGSGIHRSVIEWLDLQDFTEHVVSNKPEAKEFRQEDLILKIENENIAVYRIEGMDNNKASFDVLRTYPTTKDIEKMTLVKEGELVWENSEFFNIPEK
>NZ_LN831776.1|WP_020433679.1|4921087_4921852_-|glucose-1-dehydrogenase
MGKLEGKVAFITGGNSGIGLATAKLFVNEGAKVVITGRNQDTLNAAVEELGAASALGVQADTTDPASLEQAVAAAVERFGTLDVVFANAGISGYTPVGGTELSLFEKVLRTNVTGVFFTVQAAVPHLKEGASVILNSSVLAEAGSPGTSAYAASKGAVSSMARVLVSELAPRGIRVNTISPGATRTPIWGNAEGLAAKEAVLTRSVPLKRLGEPEEIAQVAVFLASDAASYVNGADIGVDGGSGSSPFGAPIYK
>NZ_LN831776.1|WP_020433680.1|4922042_4922633_-|isochorismatase-family-protein
MGNVKEPEELNAATTALVVIDLQNGIASTGRELHPYPVEQVIRNADNLVKAFTEKGAFVVLVRVSTLDGKDMLKPKTDLQVNPPQYPEGWDQIVPELAKYQGTYTLAKHQWGAFFGTDLDLQLRRRGIRTIVLCGISTSIGVDTTAREAYQLGYDQVFAEDAMGASSREEHEFVCKTIFSRIGRIRTSAEAAASLT

Crispr_ID: NZ_LN831776_49

• CRISPR_ID: NZ_LN831776_49
• CRISPR_location: 5036105-5036188
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: RT

Consensus repeat of NZ_LN831776_49

Consensus_repeat	Method
TCCCGGGCAAATCAAAGGTATTTATA	CRISPRCasFinder

spacers of NZ_LN831776_49

>49.1|5036131|32|NZ_LN831776|CRISPRCasFinder
ATTTATACCTCTGATTTCGCCAAACAGACCGG

CRISPR arrays and Neighbor proteins around NZ_LN831776_49

CRISPR arrays

The CRISPR arrays of NZ_LN831776_49

>merge|NZ_LN831776|49|5036105-5036188|CRISPRCasFinder
TCCCGGGCAAATCAAAGGTATTTATAATTTATACCTCTGATTTCGCCAAACAGACCGGTCCCGGGCAAATCAAAGGTATTTATA

>NZ_LN831776|49|50|5036105-5036188|CRISPRCasFinder
TCCCGGGCAAATCAAAGGTATTTATA	ATTTATACCTCTGATTTCGCCAAACAGACCGG
TCCCGGGCAAATCAAAGGTATTTATA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020430722.1|5034451_5035882_-|PAS-domain-S-box-protein	unknown	unknown	gnl|CDD|214624
NZ_LN831776.1|WP_020430720.1|5034043_5034436_-|ATP-binding-protein	unknown	unknown	gnl|CDD|379279
NZ_LN831776.1|WP_020430717.1|5032003_5034022_-|methyl-accepting-chemotaxis-protein	unknown	unknown	gnl|CDD|223910
NZ_LN831776.1|WP_046507238.1|5031732_5031990_-|STAS-domain-containing-protein	unknown	unknown	gnl|CDD|132914
NZ_LN831776.1|WP_020430726.1|5037279_5039004_-|assimilatory-sulfite-reductase-(NADPH)-hemoprotein-subunit	unknown	unknown	gnl|CDD|237402
NZ_LN831776.1|WP_020430706.1|5026494_5027400_+|sugar-phosphate-isomerase/epimerase	unknown	unknown	gnl|CDD|224007
NZ_LN831776.1|WP_039790096.1|5028041_5031164_+|response-regulator	unknown	unknown	gnl|CDD|274362
NZ_LN831776.1|WP_020425999.1|5045612_5046905_-|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	gnl|CDD|275209
NZ_LN831776.1|WP_020430730.1|5041873_5043043_+|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|366166
NZ_LN831776.1|WP_020426813.1|5048715_5051970_-|PAS-domain-containing-protein	unknown	unknown	gnl|CDD|380161
NZ_LN831776.1|WP_039790103.1|5039042_5040902_-|assimilatory-sulfite-reductase-(NADPH)-flavoprotein-subunit	unknown	unknown	gnl|CDD|273882
NZ_LN831776.1|WP_020430712.1|5031249_5031654_+|CBS-domain-containing-protein	unknown	unknown	gnl|CDD|341404
NZ_LN831776.1|WP_020430708.1|5027472_5027907_+|VOC-family-protein	unknown	unknown	gnl|CDD|319899
NZ_LN831776.1|WP_020426812.1|5047655_5048630_-|aldo/keto-reductase	unknown	unknown	gnl|CDD|381313
NZ_LN831776.1|WP_020430724.1|5036358_5037105_-|type-I-methionyl-aminopeptidase	unknown	unknown	gnl|CDD|235576
NZ_LN831776.1|WP_020430729.1|5041127_5041721_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_LN831776.1|WP_020430732.1|5043058_5043517_-|signal-peptidase-II	unknown	unknown	gnl|CDD|376504
NZ_LN831776.1|WP_020430702.1|5023021_5024827_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_020430733.1|5043710_5044415_+|DUF421-domain-containing-protein	unknown	unknown	gnl|CDD|225205
NZ_LN831776.1|WP_020430704.1|5024813_5026433_+|response-regulator	unknown	unknown	gnl|CDD|381091

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831776.1|WP_020425999.1|5045612_5046905_-|group-II-intron-reverse-transcriptase/maturase	RT	pfam00078_RT_CAS-I:CAS-III	9.8e-52	170.3	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020430722.1|5034451_5035882_-|PAS-domain-S-box-protein	gnl|CDD|214624	smart00331, PP2C_SIG, Sigma factor PP2C-like phosphatases.	7.0951e-22
NZ_LN831776.1|WP_020430720.1|5034043_5034436_-|ATP-binding-protein	gnl|CDD|379279	pfam13581, HATPase_c_2, Histidine kinase-like ATPase domain.	1.14031e-17
NZ_LN831776.1|WP_020430717.1|5032003_5034022_-|methyl-accepting-chemotaxis-protein	gnl|CDD|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	1.06421e-51
NZ_LN831776.1|WP_046507238.1|5031732_5031990_-|STAS-domain-containing-protein	gnl|CDD|132914	cd07043, STAS_anti-anti-sigma_factors, Sulphate Transporter and Anti-Sigma factor antagonist) domain of anti-anti-sigma factors, key regulators of anti-sigma factors by phosphorylation. Anti-anti-sigma factors play an important role in the regulation of several sigma factors and their corresponding anti-sigma factors. Upon dephosphorylation they bind the anti-sigma factor and induce the release of the sigma factor from the anti-sigma factor. In a feedback mechanism the anti-anti-sigma factor can be inactivated via phosphorylation by the anti-sigma factor. Well studied examples from Bacillus subtilis are SpoIIAA (regulating sigmaF and sigmaC which play an important role in sporulation) and RsbV (regulating sigmaB involved in the general stress response). The STAS domain is also found in the C- terminal region of sulphate transporters and stressosomes.	1.16426e-22
NZ_LN831776.1|WP_020430726.1|5037279_5039004_-|assimilatory-sulfite-reductase-(NADPH)-hemoprotein-subunit	gnl|CDD|237402	PRK13504, PRK13504, NADPH-dependent assimilatory sulfite reductase hemoprotein subunit.	0
NZ_LN831776.1|WP_020430706.1|5026494_5027400_+|sugar-phosphate-isomerase/epimerase	gnl|CDD|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	0.000125263
NZ_LN831776.1|WP_039790096.1|5028041_5031164_+|response-regulator	gnl|CDD|274362	TIGR02956, sensor_protein_TorS, TMAO reductase sytem sensor TorS. This protein, TorS, is part of a regulatory system for the torCAD operon that encodes the pterin molybdenum cofactor-containing enzyme trimethylamine-N-oxide (TMAO) reductase (TorA), a cognate chaperone (TorD), and a penta-haem cytochrome (TorC). TorS works together with the inducer-binding protein TorT and the response regulator TorR. TorS contains histidine kinase ATPase (pfam02518), HAMP (pfam00672), phosphoacceptor (pfam00512), and phosphotransfer (pfam01627) domains and a response regulator receiver domain (pfam00072). [Signal transduction, Two-component systems].	2.4442e-53
NZ_LN831776.1|WP_020425999.1|5045612_5046905_-|group-II-intron-reverse-transcriptase/maturase	gnl|CDD|275209	TIGR04416, hypothetical_protein, group II intron reverse transcriptase/maturase. Members of this protein family are multifunctional proteins encoded in most examples of bacterial group II introns. These group II introns are mobile selfish genetic elements, often with multiple highly identical copies per genome. Member proteins have an N-terminal reverse transcriptase (RNA-directed DNA polymerase) domain (pfam00078) followed by an RNA-binding maturase domain (pfam08388). Some members of this family may have an additional C-terminal DNA endonuclease domain that this model does not cover. A region of the group II intron ribozyme structure should be detectable nearby on the genome by Rfam model RF00029. [Mobile and extrachromosomal element functions, Other].	0
NZ_LN831776.1|WP_020430730.1|5041873_5043043_+|alpha/beta-fold-hydrolase	gnl|CDD|366166	pfam00561, Abhydrolase_1, alpha/beta hydrolase fold. This catalytic domain is found in a very wide range of enzymes.	4.94306e-10
NZ_LN831776.1|WP_020426813.1|5048715_5051970_-|PAS-domain-containing-protein	gnl|CDD|380161	NF033092, HK_WalK, cell wall metabolism sensor histidine kinase WalK. This model describes WalK as found in Staphylococcus aureus (sp|Q2G2U4.1|WALK_STAA8). A shorter version, as found in Streptococcus pneumoniae, called WalK(Spn) or VicK, is not included. WalK is part of a two-component system and works with partner protein WalR.	1.76692e-59
NZ_LN831776.1|WP_039790103.1|5039042_5040902_-|assimilatory-sulfite-reductase-(NADPH)-flavoprotein-subunit	gnl|CDD|273882	TIGR01931, Sulfite_reductase_flavoprotein_alpha-component, sulfite reductase [NADPH] flavoprotein, alpha-component. This model describes an NADPH-dependent sulfite reductase flavoprotein subunit. Most members of this family are found in Cys biosynthesis gene clusters. The closest homologs below the trusted cutoff are designated as subunits nitrate reductase.	0
NZ_LN831776.1|WP_020430712.1|5031249_5031654_+|CBS-domain-containing-protein	gnl|CDD|341404	cd09834, CBS_pair_bac, Two tandem repeats of the cystathionine beta-synthase (CBS pair) domains present in bacteria. The CBS domain, named after human CBS, is a small domain originally identified in cystathionine beta-synthase and is subsequently found in a wide range of different proteins. CBS domains usually occur in tandem repeats. They associate to form a so-called Bateman domain or a CBS pair based on crystallographic studies in bacteria. The CBS pair was used as a basis for this cd hierarchy since the human CBS proteins can adopt the typical core structure and form an intramolecular CBS pair. The interface between the two CBS domains forms a cleft that is a potential ligand binding site. The CBS pair coexists with a variety of other functional domains and this has been used to help in its classification here. It has been proposed that the CBS domain may play a regulatory role, although its exact function is unknown. Mutations of conserved residues within this domain are associated with a variety of human hereditary diseases, including congenital myotonia, idiopathic generalized epilepsy, hypercalciuric nephrolithiasis, and classic Bartter syndrome (CLC chloride channel family members), Wolff-Parkinson-White syndrome (gamma 2 subunit of AMP-activated protein kinase), retinitis pigmentosa (IMP dehydrogenase-1), and homocystinuria (cystathionine beta-synthase).	1.16941e-56
NZ_LN831776.1|WP_020430708.1|5027472_5027907_+|VOC-family-protein	gnl|CDD|319899	cd06588, PhnB_like, Escherichia coli PhnB and similar proteins. The Escherichia coli phnB gene is found next to an operon of fourteen genes (phnC-to-phnP) related to the cleavage of carbon-phosphorus (C-P) bonds in unactivated alkylphosphonates, supporting bacterial growth on alkylphosphonates as the sole phosphorus source. It was originally considered part of that operon. PhnB appears to play no direct catalytic role in the usage of alkylphosphonate. Although many of the proteins in this family have been annotated as 3-demethylubiquinone-9 3-methyltransferase enzymes by automatic annotation programs, the experimental evidence for this assignment is lacking. In Escherichia coli, the gene coding 3-demethylubiquinone-9 3-methyltransferase enzyme is ubiG, which belongs to the AdoMet-MTase protein family. PhnB-like proteins adopt a structural fold similar to bleomycin resistance proteins, glyoxalase I, and type I extradiol dioxygenases.	1.76372e-47
NZ_LN831776.1|WP_020426812.1|5047655_5048630_-|aldo/keto-reductase	gnl|CDD|381313	cd19087, AKR_AKR12A1_B1_C1, AKR12A, AKR12B, AKR12C families of aldo-keto reductase (AKR). Streptomyces fradiae TylCII, Saccharopolyspora erythraea EryBII, and Streptomyces avermitilis aveBVIII are founding members of aldo-keto reductase family 12 member A1 (AKR12A1), B1 (AKR12B1), and C1(AKR12C1), respectively. TylCII acts as a NDP-hexose 2,3-enoyl reductase. EryBII is a mycarose/desosamine reductase involved in L-mycarose and D-desosamine production. aveBVIII functions as a dTDP-4-keto-6-deoxy-L-hexose-2,3-reductase.	6.59671e-173
NZ_LN831776.1|WP_020430724.1|5036358_5037105_-|type-I-methionyl-aminopeptidase	gnl|CDD|235576	PRK05716, PRK05716, methionine aminopeptidase; Validated.	8.87635e-146
NZ_LN831776.1|WP_020430729.1|5041127_5041721_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.42832e-11
NZ_LN831776.1|WP_020430732.1|5043058_5043517_-|signal-peptidase-II	gnl|CDD|376504	pfam01252, Peptidase_A8, Signal peptidase (SPase) II.	2.5025e-32
NZ_LN831776.1|WP_020430702.1|5023021_5024827_+|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	1.01813e-40
NZ_LN831776.1|WP_020430733.1|5043710_5044415_+|DUF421-domain-containing-protein	gnl|CDD|225205	COG2323, COG2323, Predicted membrane protein [Function unknown].	1.0592e-57
NZ_LN831776.1|WP_020430704.1|5024813_5026433_+|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.36794e-37

Protein sequences

>NZ_LN831776.1|WP_020430722.1|5034451_5035882_-|PAS-domain-S-box-protein
MAVDKQCKNLFRSPSPAQCMEHYGCIYENNHLITLLVDPADGSITDANRAACEFYGYPLRIFRKLHITDLQADQTSGMVKFIEHGMPGGEHGRNRVFMDKHLLAGGQQIDVEIHTGMMSMLGKSCIYTVIHDISERVRSEQRLRESEERYRDLVELCPEAILVYSGGMILFANKQSEKMFGKKKKEMIGQRIEAFFSEEYLKSAKYKKLMTWGSTAKERFRIEQRLIRYDNRIFDVEISGVPIIYEEEKALQLVLRDITESKKEVERAVKLQNHRHTVVFPLEDKAELEKLYIPARTLSGDFFIFHKIDEERVIGMIGDVTGKGITAALNISALRVLFADCLEVTVDPLQAIKELNQKAMLHLGEDYIAGCCFQLDFGAGVLKAAGAGINEFIYVPKDQESQCLTVRGAPLGMFGNSEFEEITVPFSSGDRFCFYSDGMELLFDTQELSRSYEYLTDKIAEASLQDDCTWLNLSIK
>NZ_LN831776.1|WP_020430720.1|5034043_5034436_-|ATP-binding-protein
MNAVQKEIRLYGLEQHQRIIDGIIQELGLEDYAFDIRLILIEAITNAYYHGNLSDCTKPIIIRYLLSGKRLELQVEDSGEGTGSLVFPETISGDELLDEGGRGLYLIRCFSDKAEMIRNTMYISKCVCPS
>NZ_LN831776.1|WP_020430717.1|5032003_5034022_-|methyl-accepting-chemotaxis-protein
MKLSLKVKISILLFLIISVPLAISGLISHNLASNALQQTIEEELRDTTASAAKAVDSELEAVESYLSIASKNDTLAAFAANPAGEAAKKLAHTYISGIQQDHAKLLESLIIAGTDGQVLLTSSPENPGLDVRDQDYFQQALQGKEAVSEVLFSKESNQHVVAIARPLEHDGHITGVLIGTVVFNSLSSPVAEVKIGDSGYGYMTDRTGLIVYHPDQGKILKETLDGNSNKELNALVQVMKSGKASDGFYTYEGVHKYMSFQPAGNWVVATTANVQDYMAPATEIRNTTLIIVIAFILIALLVAYFFTTRNIVHPIIKLEQAMSRAGEGNLTVHTSIRSGDELQELSEAFNTMIDKQKAIIEKVRAGSVSLTSMSEEMAASSEEISASIQEISSSTQEIAAGAENNNQSVVNASQVLVQLSSLVQMAQSKAAATSGNADVTNQAAQRGRAQVMDTVQAMNTISSSTQETEEQLQAVSELSDQVSTIIGTINAIAQQTNLLALNAAIEAARAGEHGRGFSVVAEEVRKLSDETHKQATEISALVSDMVSRITQAVDSMRGATEAVEGGVRVVTETDHAFVHIINSVELITGSVKEILDITQDEVATSDQIIKLIDSMGSISELAAINSENVSSATEEQAATVTNFAASAQEVSAMANELEILVEKFIIRGEQVE
>NZ_LN831776.1|WP_046507238.1|5031732_5031990_-|STAS-domain-containing-protein
MPEMFSVEEASEFREKIRGHIDGGFSSFVLDFGGCAFIDSTGLGVIVSSYKKCVENGGTIKLKALNANVLKIFELTRLTHVFEIL
>NZ_LN831776.1|WP_020430712.1|5031249_5031654_+|CBS-domain-containing-protein
MEISAFLLPKDQVSYITSSISMLEALEQLEHHYYSAIPIINEEGKYVGTLSEGDLLWKFKNTAGLNFENMREVTVSEIQQHVHNESVEIHAQMEDMLTLAADQNFVPVVDDKGIFLGIIRRKDIIEYYTRNITD
>NZ_LN831776.1|WP_039790096.1|5028041_5031164_+|response-regulator
MMKKPFTFFLKNIVIVLLYLAVLSAIRYLWFTTYVAPEHPQAVQGVLDLRSFQIGDSRSIPLDGEWEFYPDELLTHKDFPQPDTRRHYAMVPGDWRNGFPEKGHASFGTGTYKLRILTGTPLDEPYGFWIQRIQAASEIEINGQKEPSVGRLAESKEDYIPDAPSYTATYIAGDHREIELLVRVSNFDHPQKGGIVRSIRFGTQAAIDTERWYSIGFQLVAFIILLLHALYAGILYCFNRQNVFLLFFLLLVAVGISIISDNDILLRLWLPINYTWLLKIKLLSYMWLSYFMLQLSQSFSGRRRPHTGILFRSYAAVLGLYSAFIVVMPAEIIFQTILLFSILYLLPVAGVVWKIVQMVLGKQEDAVFLLFAAVAILSSVLWGVVESRGNTSNFFYPVDIIAAIIGFSAYWFKRYFRNSEENIKLNRQLQENDRLKDQFLANTSHELRTPLHGIISIAQTVAAKEHSVMDSKSVQDMDLLLTISRRMSHLLNDLLDVTRLQDKRIELQREPLSIQSLVSGVIDMFEFMTEGRALTLKNNIADSLPPVFADEKRLVQILFNLLHNAVKYTIEGSIAVSAETQGKEMLIHVADTGAGMNEETLSRIFKRYEQGQQGINDGGGIGLGLSICKQLVELHHGTLTVRSQPGQGSEFTFTLPLAKGTDQPASALSSQEMPKNTEPARPSVPAHSPLADLSAIWSAAHSGESEGAGRRIHILAVDDDSVNLKVLASILSSENYNIRTALGAHEALNLLGTEQWDLLIADVMMPHISGYELTRIVRERFSLSELPILLLTARTQPEDIYTGFLSGANDYLVKPVDGLELKYRVRSLTGLKQSIDEMLRMEAAYLQAQIQPHFLFNTLNSIMALSEIDTAKMRDLSEAFSSYLRISFDYMNSHQRVALSHELELVRAYVYIEQARFEERLAVEWDIEDGINTALPPLTLQPLVENAVRHGLLSRSRGGLLTIRIRSSGGFTFFEVRDNGKGMTQEQVSHLLDHSRKVSGGIGLLNTNRRLTQLYGRGLSIQSEPEQGTSVSFTIPDPGK
>NZ_LN831776.1|WP_020430708.1|5027472_5027907_+|VOC-family-protein
MAINVYFNFNGNAREAVEFYAEVFGTEAPRIMTFGEAPPDPSHPLPEEAKHLVMHAMLFIDGSPVMFSDVFPGMPYVEGNNVNLTLTNDDAGKIKDWFNKLKEGGNVIMELQETFWSKCYGSLKDKFGIIWQLSHDNGQGAGNA
>NZ_LN831776.1|WP_020430706.1|5026494_5027400_+|sugar-phosphate-isomerase/epimerase
MHQFMIGQYGGFDSHKYHRDFKAAFYGIEACSFPGDEDCRLLMEESKSKGFRVGVHFPFRANGSAIRDALFLSSDPGEREAAFEQIRTELEYLTVLKPEYVLFHYPKPVILDDRVDWKLWRFGDRREYIFESECTLSGLIERSESLFEWLDLRSREYHFTPILEFDALNRYVYEHDFFENLLLKYPQIQLCLDTARLHLQDKLDPRFDAKAVLRKYAKYAGLIHLSTVQVNQAVQNSHYPVLPELSVQDGWAPIAEYLQIIRGENSRVKIMFEHRSDLITEDQLQQCYDWVDAIVNGSVYL
>NZ_LN831776.1|WP_020430704.1|5024813_5026433_+|response-regulator
MNHYKVVLVEDEIPARTVFRHFIEERGDLFTLVGEAEDGQDGLELFLKHKPELIVTDITMPGMNGLEMLREIEKSGERPPQIIILTCHQDFHYAQQAIHLKAASYLIKDDCLSDPGLLTRTMEQLASQVHSIDETREKQLQLEQQVRLSEVEIEQSLFLDMLLNPAAEAKWLRTLEESQLPVQEGRFKVLLLELDRGSLRFPIGQIEELKLWQFAGVNVLKELLGGIGAHKVIALDKGRFLAVYTDALKLERPGFLEQVLESFAANLKMKCFALQCRFEQGLRGRPEALKRLASAPYPFFYRSDESIAIEEWEQFAFFQRIPEPVSRFWSKVLKKALLEPHLSAAALEQERSSLFRQAIEHGWEPEQIKSLYLRVFLDMSHTVIGAEGGAELEAALRKKLELCQTFGSVHDTTCAYFHKLQQLQEGGKKIDSSISRIIQHMREDLSYPYKLEELAASMNYSVPYFSSMFKKAVGESFVQYLTRLRIEKAKLLLLTTDHKTFEISESIGFENYRSFNRIFKKETGVSPSDYRRNGAAMSR
>NZ_LN831776.1|WP_020430702.1|5023021_5024827_+|sensor-histidine-kinase
MSSTFFSFLRRSFYFKMILVMLAVSVIPLIVLSIISVSVSSNTVEKQVNRLNAQLVNQVVDRIELTMTRLRELSEQYSRISSIQSALVSPSAQYFEEVVRKKELISVLSNASAVIGNVEGLQVYSAITGEVLSSTEAPAMLEDSPYRPLIEAYLSSGKANLFLDKHALPDLAILDSSTYYISRVPFDLYEDLKGVLLISMSNDQYQRQIENIQLGNRGSISLLTDDGMTIATTSRLEPKEDTGRVQNILKHWKELDRPNQFAVGSSIVSVKQTSTYDNWIVVSEIPSKELTASAEIIRRTVAYFLGILVFLGALCVVGFGYQLYRPLQAVKRQVDAIKKGHFDARVTHFANNEIGDLGRMLNTMAVRIQDLLADLHDSEELKHKLEIRALQSQINPHFMYNTLNTIRMFAMMKDYEKINTLMGRLVALLRYSMENYEQTVQLQQELDYLADYVGLLNMRYKCQVHLEAEIEEPLRGMQIPKLSLQPLIENSVFHGILPNKTAEGHIKVHVFTDSLQNHIVIEVSDDGVGLEEAALGTLQLHLLREESTENIGLQNVWMRMKLLFGKAAQILLLSPPGEGMTIRITLPIESVPMKEEQHEPL
>NZ_LN831776.1|WP_020430724.1|5036358_5037105_-|type-I-methionyl-aminopeptidase
MIIMKTMEEIEKMRAAGKILAECHRQIAQMIKPGITTWEIDQFAEKFILSQGATPEQKGYHGYPYATCASVNDVICHGFPKREELKDGDIVTIDMVVNLNGWLADSAWSYAVGNISEQAEKLLNTTKESLFKGIEQAVAGNRIGDVAHAVQVYAESNGFSVVRDFIGHGIGSEMHEAPEVPHYGPAGKGPRIKEGMVFTIEPMLNTGSYRTKVDADGWTARTIDGGLSAQYEHTLAITPQGTIILTEL
>NZ_LN831776.1|WP_020430726.1|5037279_5039004_-|assimilatory-sulfite-reductase-(NADPH)-hemoprotein-subunit
MANNESAVKPVGGPPSDVEHIKLESNYLRGALVETLSNPITGSLPEDDNRLLKFHGSYMQDDRDLRSERERSKLEPAFQFMLRVVAPGGVATPAQWLVMDELARKYGNGTLRLTTRQAFQMHGVLKWNLKKTIKTINDALMTTLAACGDVNRNVMSGPNPYQSEVHAEVYEWARRISDHLSPRTPAYHEIWLDGEKVVDSKEGVEVEPIYGPVYLPRKFKIGLAVPPSNDVDVFSQDLGFIAILEDGKLAGFNVSVGGGMGMTHGDTNTYPQLGRVIGFCRPEQMIDLAEKTVTIQRDYGNRSVRKNARFKYTIDRHGLEWFTGELQHRLGWALEPARSYHFDHNGDRYGWVKGVNGKWNLTLYIQSGRIQDTETSQLMTGLREIAKIHGGDFRLTPNQNLIIANVSSVKKRKVAELAKQYGLTDGAHHSALRRSSMSCVALPTCGLAMAEAERYLPQLLDKLELIIDEAGLRGEEIIIRMTGCPNGCARPALGEISFIGKAPGRYNMYLGAGFTGDRLNKLYKENIDEKEILETLEPIIHRYAKERQSGEHFGDFVIRSGYVKAVTSGLNFHD
>NZ_LN831776.1|WP_039790103.1|5039042_5040902_-|assimilatory-sulfite-reductase-(NADPH)-flavoprotein-subunit
MQLQVTNSPFNEEQVELLNRLLPTLTQTQQIWLGGYISALTLQGAAAVSAAAPAVLAAPSASTAAAGGAAEPARSREVTVLFGSQTGNCQRLASSLSGKLKEQGFEITVSAMNSFKPNTLKKVENLLILVSTHGEGEPPDNARSFHEFLNSKRAPRLEHLRFSVLALGDTSYEFFCQTGKDFDQRLEELGGQRLIPRVDCDLDYDEPVAAWMEQVITALNGAGSAPAIAEEAVLAAEHAESLQSAYSRNHPFHAEVLENLNLNGRGSDRETRHLELSLAGSNITFEPGDALGVYPENHPRLVEEIIAAMGWNPEEPVPLNKKGEEGTLREALLRHYEITVLSKPLLEQAAKLSPAAGLHELLLPDRAPQLKEYIQGRDLLDLVQDFSPWDVPARSFVTILRKLPARLYSIASSYNANPEEVHFTVRAVRYESHGRERYGVCSVHCAERVQPGDTLPIYIQNNPNFKLPANPEVPVIMIGPGTGVAPFRSFLEEREEQDAEGKTWLFYGDRHFVTDFLYQTDWQRMLKDGVLTKLDVAFSRDTEEKVYVQHRILEHSRELYTWLQEGAHVYVCGDEKHMAHDVHSALISVIQAEGGLSPEAAAAYLDHLQQEQRYQRDVY
>NZ_LN831776.1|WP_020430729.1|5041127_5041721_-|TetR/AcrR-family-transcriptional-regulator
MSRETDLRVVKTKKLIRDALVSLIAEKGFDSVTVNDIAGRAQINRSTFYLHYTDKYELLEKITAEITGKLMALIIPAAHVQGGLLGVGDLTRDLEKILAAIAEDALFYQIMLSGRGVHSFRFDLGNLLKQKLDEGFREQPLISKDLFVELLSSLYLGAIAWWLDNGMKYSPAFMAGQLVQLMTMGPVKVSGLVSGPI
>NZ_LN831776.1|WP_020430730.1|5041873_5043043_+|alpha/beta-fold-hydrolase
MAERQRTTADFPVGFYEELHPDFSINFQMNRFYSWTNDLEMLEEMRAAAPGIHNYAELIEICLKLGQQAVAADKKLKAANYLRGAEFYMPEGHPLKHTSRQQFIVLTRAHYQVEDNQHFDIPYGKGFLSAYRFSPEVPAKGSIVLFGGFDSYIEEIFLMALVFKDAGYDVVCFDGPGQGAALEDWQLPMTHEWEKPVATVLDFFNLQEVTLIGLSLGGYLALRAAAYETNRVKRVVADDICTDFYKVLLRQTGPLEDSISTLMAKENEAEINALFSRLMKENLMLEWGITQGMHVTGSQTPYGFLKQSMLYTTAGISPLLSQDVLLLAAQEDHYIPLVQFGEQTGSLTSVRSLTTRLFTRKEQAQNHCHVGNIGLSIHVMLHWLQQWEA
>NZ_LN831776.1|WP_020430732.1|5043058_5043517_-|signal-peptidase-II
MIFYVITILVIIADQAAKWGVRSNMQLGETVQVWSGHLQFTYYENSGAAFSSFQGYGKYFAIIAVLFVAGIFYYRRKGELRGPILEAATGFLAGGAIGNAIDRVIYHQVTDFLVFGSRGGILNLADLAINAGGLLVVVHLLKEPLKRVMIRR
>NZ_LN831776.1|WP_020430733.1|5043710_5044415_+|DUF421-domain-containing-protein
MDYVSVLVKLTAGFVGLWAMARLLGKKEISALTPFDFISAVILGDLVGNTIYEPDKSVLLLLFALAVWTVLSIIFEKITQRVRKLRKPLEGEPEILIRDGKLDLTKLRKNNLDFEQLRMMLRAKDTFSMNEVAYAIYETNGSLSILKKPQFEPATRKELDIKPQHTRLPRSLVEAGEVQRAALASLGHDETWLRRKLQEEGCPNLDSVAYAEINEEGKLAIIPSTSQHAKPGEY
>NZ_LN831776.1|WP_020425999.1|5045612_5046905_-|group-II-intron-reverse-transcriptase/maturase
MNAKGLTTPKEKVQELQEKLGHAAKENKKRKFHALYDKVYRPDVLCEAWKRVKANKGAAGVDAVTLADIEERGETNFLKTCERELKEGSYHPQPVRRHYIPKKDGKPRPLGIPTVRDRVIQMATKLVIEPIFEADFEEVSFGFRPKRSAKGALERIRKACNRKGNWVVDVDIQGYFDNINQEKLMKLVQMRINDRRILKLIRKWLQAGVMEEGNVRRSDLGTPQGGVISPLLANIYLNYFDRLWEKHGSGLGELTRYADDFVVVCKTKKDAEHAYELISRIMERLELTLHPTKTRIVGLWTGDEGFDFLGMHHRKTKAETSQGKVYYTTQQWLTKKAEERIRGVVKERLAPPSMRSRTLAEQVEWLNPKIQGWRNYYYTNYSQKRLAKLDWYILQRLTRWYAKKRQRGRWMRSRSEVKYLTIQYGLKTLL
>NZ_LN831776.1|WP_020426812.1|5047655_5048630_-|aldo/keto-reductase
MKYSYLGKSGLKVSQLCLGTMNFGPETEEKEAFRIMDAALDAGINFFDTANVYGGNDRRGWTEEIIGRWFQQGGGRREKVVLATKVYNDMFDEQDGPNSGAGLSAYKIRRHFEGSLKRLQTDHIELYQMHHIDRNVSWDELWGAFEILVSQGKADYIGSSNFAGWHIAAAQAKAKERHFLGLVSEQHLYNLLERTPELEVLPASQELGLGVIPWSPLAGGLLGRNALSKTGVRSARSAKLEQHRSQLEQFSALCKELGEHEDQVALAWVLANPAVTAPIIGPRTLEQFEDSLRVTEIVLEADVLKKLDEIFPGPGRPAPEAYAW
>NZ_LN831776.1|WP_020426813.1|5048715_5051970_-|PAS-domain-containing-protein
MRTAKPSNHSIKTKYYRIITLLFLLLVVTVTVLFFYINSQQSKLKAEREVLQTKAHTIDRLAGALNEVFFRARGYVALKNSNELSLLNTALENLDGILDQYSTLNLSAEEAEYRDALSAFYTNYKSKTLPKAIQLVESDDYEGIRTLSQSGSTQALNDFLAYTKAFKDNSDKQLSEMADRSIRKADGYTVAAFGISAFLLLFFTLMIWRMLKVLIDPIVRLEEATHSLAAGEAVLLGRLHKQDEIGRLYEAFLNMAHSIQDKEEELTMQNEELQAQQDELQDQQFKLERSLIEIESIMKALNQTSAVGILSDKGLFTYANDNLSKYTGYSHSEMIGYPFRLLELLNITDSQLEQIFFKLSTGGIWSGEVEALVKDGSASVWLHMTVMPYLNDEGKVYQYILIANNITSLKSAQQQLAVTLRNTEQTTVMLERYNQLNHELTYTLDKQEFAGKFSRFMNQIYAFDSSLFFLVKDKIAVVKGVPQEKVEQYLDHHHLDMLHRLKEEKSYIVKRTGSPREQGISPDEVLCYDFYTSVVGGNDEILAVFCGSRIGHAFTEEEISEIQGLASRVALAIERIMMYEEIEHGRKLNQDIVNNVNEGIQFVNTEGVMQHINKALSQLFHYEWAEGSLIPAEAWLDAFTGKSNESAELRSFYENAIAESALDSSTMKYSLGKEEIQHVDVYAIPVLRREDRIGTLFVHRDITREYELDVMKSELVSTVSHELRTPLSSVLGFTELLLSKTMKPEKQLKYLETIHKEAKRLTELINDFLDLQRMESGTQQYNVEPAHLSEIVLGVIDQYKLSSTHHILFEDEAVHDEVAVDRDKIVQVLTNLLSNAIKFSPGSHEVKVMLHNEPGRILVRIQDQGLGIPKNQIGQLFQKFRRVDNSASKRIGGTGLGLAICKEIIEKHKGTIGIDSVEGEGSTVWFSLPVQVAEESRPVEEMSKWGADKEQKPSVMIVEDDYSLSLLLSEELKGKGFRVTHHYHPQKAFDQALKSPFVAIVVDLMLGVELDGWDLIRMLKNDPRTEKVPIVISSALDQTDKSLLENVKTYLTKPYPPGELSKTLQEIVEIKLKSGEVLFPGNDC

Crispr_ID: NZ_LN831776_50

• CRISPR_ID: NZ_LN831776_50
• CRISPR_location: 5074113-5074186
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_50

Consensus_repeat	Method
TTAAGTTACCTTTTTCCACTTAA	CRISPRCasFinder

spacers of NZ_LN831776_50

>50.1|5074136|28|NZ_LN831776|CRISPRCasFinder
ACCTCGCGATTCTTGATTTCTGAGGAAT

CRISPR arrays and Neighbor proteins around NZ_LN831776_50

CRISPR arrays

The CRISPR arrays of NZ_LN831776_50

>merge|NZ_LN831776|50|5074113-5074186|CRISPRCasFinder
TTAAGTTACCTTTTTCCACTTAAACCTCGCGATTCTTGATTTCTGAGGAATTTAAGTTCCCTTTTTCCACTTAA

>NZ_LN831776|50|51|5074113-5074186|CRISPRCasFinder
TTAAGTTACCTTTTTCCACTTAA	ACCTCGCGATTCTTGATTTCTGAGGAAT
TTAAGTTCCCTTTTTCCACTTAA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020427754.1|5069823_5071677_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270300
NZ_LN831776.1|WP_020427753.1|5071778_5072672_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_141639074.1|5079483_5080173_-|hypothetical-protein	unknown	unknown	gnl|CDD|224578
NZ_LN831776.1|WP_046504627.1|5082339_5083689_-|tellurium-resistance-protein-TerF	unknown	unknown	gnl|CDD|378410
NZ_LN831776.1|WP_020427752.1|5072686_5073646_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_LN831776.1|WP_046504623.1|5074447_5075362_-|fumarylacetoacetate-hydrolase-family-protein	unknown	unknown	gnl|CDD|223257
NZ_LN831776.1|WP_046504625.1|5081069_5082206_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379240
NZ_LN831776.1|WP_020427739.1|5083837_5084452_-|50S-ribosomal-protein-L25	unknown	unknown	gnl|CDD|235534
NZ_LN831776.1|WP_020427743.1|5080250_5080880_-|YhbD-family-protein	unknown	unknown	gnl|CDD|379048
NZ_LN831776.1|WP_046507254.1|5075445_5076303_-|SMP-30/gluconolactonase/LRE-family-protein	unknown	unknown	gnl|CDD|369882
NZ_LN831776.1|WP_020427758.1|5063464_5064646_+|MFS-transporter	unknown	unknown	gnl|CDD|225371
NZ_LN831776.1|WP_020427759.1|5062907_5063414_+|YbaK/EbsC-family-protein	unknown	unknown	gnl|CDD|239825
NZ_LN831776.1|WP_020427760.1|5062315_5062750_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224759
NZ_LN831776.1|WP_020427756.1|5066551_5067949_-|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_052741505.1|5078822_5079491_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427748.1|5076495_5077122_+|hypothetical-protein	unknown	unknown	gnl|CDD|227169
NZ_LN831776.1|WP_020427755.1|5067941_5069693_-|histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_020427747.1|5077168_5078704_-|MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_LN831776.1|WP_052741504.1|5064857_5066555_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270298
NZ_LN831776.1|WP_046507248.1|5060688_5062155_-|MFS-transporter	unknown	unknown	gnl|CDD|129794

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020427754.1|5069823_5071677_-|extracellular-solute-binding-protein	gnl|CDD|270300	cd13582, PBP2_AlgQ_like_3, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	1.47378e-26
NZ_LN831776.1|WP_020427753.1|5071778_5072672_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	7.64902e-53
NZ_LN831776.1|WP_141639074.1|5079483_5080173_-|hypothetical-protein	gnl|CDD|224578	COG1664, CcmA, Integral membrane protein CcmA involved in cell shape determination [Cell envelope biogenesis, outer membrane].	0.0012075
NZ_LN831776.1|WP_046504627.1|5082339_5083689_-|tellurium-resistance-protein-TerF	gnl|CDD|378410	pfam10138, vWA-TerF-like, vWA found in TerF C-terminus. vWA domain fused to TerD domain typified by the TerF protein. Some times found as solos.	3.2817e-97
NZ_LN831776.1|WP_020427752.1|5072686_5073646_-|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	2.492e-83
NZ_LN831776.1|WP_046504623.1|5074447_5075362_-|fumarylacetoacetate-hydrolase-family-protein	gnl|CDD|223257	COG0179, MhpD, 2-keto-4-pentenoate hydratase/2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) [Secondary metabolites biosynthesis, transport, and catabolism].	5.83257e-102
NZ_LN831776.1|WP_046504625.1|5081069_5082206_-|GNAT-family-N-acetyltransferase	gnl|CDD|379240	pfam13527, Acetyltransf_9, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	2.06798e-13
NZ_LN831776.1|WP_020427739.1|5083837_5084452_-|50S-ribosomal-protein-L25	gnl|CDD|235534	PRK05618, PRK05618, 50S ribosomal protein L25/general stress protein Ctc; Reviewed.	3.56076e-48
NZ_LN831776.1|WP_020427743.1|5080250_5080880_-|YhbD-family-protein	gnl|CDD|379048	pfam13171, DUF4004, Protein of unknown function (DUF4004). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are approximately 210 amino acids in length.	1.51022e-82
NZ_LN831776.1|WP_046507254.1|5075445_5076303_-|SMP-30/gluconolactonase/LRE-family-protein	gnl|CDD|369882	pfam08450, SGL, SMP-30/Gluconolaconase/LRE-like region. This family describes a region that is found in proteins expressed by a variety of eukaryotic and prokaryotic species. These proteins include various enzymes, such as senescence marker protein 30 (SMP-30), gluconolactonase and luciferin-regenerating enzyme (LRE). SMP-30 is known to hydrolyze diisopropyl phosphorofluoridate in the liver, and has been noted as having sequence similarity, in the region described in this family, with PON1 and LRE.	2.1488e-92
NZ_LN831776.1|WP_020427758.1|5063464_5064646_+|MFS-transporter	gnl|CDD|225371	COG2814, AraJ, Arabinose efflux permease [Carbohydrate transport and metabolism].	8.07006e-98
NZ_LN831776.1|WP_020427759.1|5062907_5063414_+|YbaK/EbsC-family-protein	gnl|CDD|239825	cd04333, ProX_deacylase, This CD, composed mainly of bacterial single-domain proteins, includes the Thermus thermophilus (Tt) YbaK-like protein, a homolog of the trans-acting Escherichia coli YbaK Cys-tRNA(Pro) deacylase and the Agrobacterium tumefaciens ProX Ala-tRNA(Pro) deacylase and also the cis-acting prolyl-tRNA synthetase-editing domain (ProRS-INS). While ProX and ProRS-INS hydrolyze misacylated Ala-tRNA(Pro), the E. coli YbaK hydrolyzes misacylated Cys-tRNA(Pro). A few CD members are N-terminal, YbaK-ProX-like domains of an uncharacterized protein with a C-terminal, predicted Fe-S protein domain.	1.24305e-69
NZ_LN831776.1|WP_020427760.1|5062315_5062750_+|MarR-family-transcriptional-regulator	gnl|CDD|224759	COG1846, MarR, Transcriptional regulators [Transcription].	1.82899e-16
NZ_LN831776.1|WP_020427756.1|5066551_5067949_-|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.09442e-46
NZ_LN831776.1|WP_020427748.1|5076495_5077122_+|hypothetical-protein	gnl|CDD|227169	COG4832, COG4832, Uncharacterized conserved protein [Function unknown].	8.93154e-65
NZ_LN831776.1|WP_020427755.1|5067941_5069693_-|histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	4.40008e-40
NZ_LN831776.1|WP_020427747.1|5077168_5078704_-|MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	2.72902e-69
NZ_LN831776.1|WP_052741504.1|5064857_5066555_-|extracellular-solute-binding-protein	gnl|CDD|270298	cd13580, PBP2_AlgQ_like_1, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	2.4072e-108
NZ_LN831776.1|WP_046507248.1|5060688_5062155_-|MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	6.80871e-71

Protein sequences

>NZ_LN831776.1|WP_020427752.1|5072686_5073646_-|sugar-ABC-transporter-permease
MGVPSGELLRGVEPVRPSRRKLQNKYKLFLLALPFLAVTFVFYYLPVSGWIYAFYDFIPGIPLSETPYVGLKWFRTLVANPTQTGEVLRVLKNTVAMSSLGLATSVFPVIFAILLTEIRAGWYRKFVQTLTTIPNFISWILVYALAFSLFSVDNGVVNHILVQLGVVSEEFNFLASSSHVWLTMIAWYWWKSLGWGAILYLAAIAGIDQELYEAAEVDGASRFRKIWHITVPGIIPTFFVLLLLSIGNFVNNGMEQYFAFQNAMNKDAIEVLDLYVYNIAFANNFPFATAVSMLKSVVSVILLFAANTLSKVVRDESII
>NZ_LN831776.1|WP_020427753.1|5071778_5072672_-|carbohydrate-ABC-transporter-permease
MRKKLKPGDALFQGIIYVLFGLFTLSCIYPFYYLFINTISSNDLSAAGDINFYPQQIHFDNYSKVLRISGLSHAALVSVYRTVAGTFLTVGASAFLGYLFTKKEMWGRQIWYRSVVVTMYFSAGLIPWYITMHNLHLTNNYLAYILPTIITPFNIILVKTFVEAIPPSLEESAAMDGAGVLRSFWSIVVPLTTPILATITIFSAVNQWNSFIDTAFLMTDTKYYTLQFLLWRYLNESSSLAALIRSSPDMAASVQNMQTPTSVRMTVTMIVVLPILIVYPFFQRFFVKGIMIGAVKG
>NZ_LN831776.1|WP_020427754.1|5069823_5071677_-|extracellular-solute-binding-protein
MKFKKLPLILLGMVLMLVLASCGGGNGNSGNSVNSGKTNTAESTGKPAAEATDAAAESAAPSDGTLDHSKPLKLTVFSTTANYAGPQTGWFAKIIKDKFNIELDIVASNLTGGDTKISAMMASGNLGDIIVFGDDKNHYPNAIKGKLLLDWTQDGLLDKYGADLTKQFPKAVEKAKVAFGGGSAVYGIGNGVATNPSGPSEGKDMTWGPDLRWDLYQQIGAPEISTIEDYLPVLKKMQELEPKNEQGKKTYAFSLWSDWDGNYKMTLAKQFANMMGYDEIPDTALYVKADEEKYYDFISEDSWYMKSLKLYYEANQLGLLDPDSLTQKFDDVVAKYKDGRLLFSWFPWLGAANYNTPERTAEGKGFALVPFKNELMYSTGFNVYGGNGIIAIGAKAKEPARIMEFLNWMYTPEGAMISAGSGTAVPNGPQGLTWDIDSSGKPVVTDFGWKAYADQQNTKVPDEYGGGDYYYGSNQMNFSFVVPAMVNPQTSEPYDHNLWTTSLERNPTKLDSDWRAKMGVLTAKEYFEKNNLLAVAPQGFTGKEPLTMDKTLEQKNKQIGTVIQQISWKMVFAKNQVEYDKLNKEMHDKVNGLGYADVMDFSVKKAAELFEARKSVK
>NZ_LN831776.1|WP_020427755.1|5067941_5069693_-|histidine-kinase
MRILKRKARRQAPAGQSLRTTLVMYLLVGTLLPLLIVGIVSYTSIYSILSGKIGSGISAGLQQEALVLENAIDNLDFASKQFALDGQIVEEMSSFLEEKQIYRKSQIMNSINQKINLVNFTNPYIGLTAYIMPGSDDPVLFTNMSTRRDFDPGRLPAFMRYNGADYYGPHGTMYAVGDNVVFSERRIVRVNGQHELYIYLETNYSLLRKIFNPQAYGMQVNHLLVNQNNTDIHVIDGELPASVVEAARASTGPAHEVLDGYHLFRYESLQGWKLVAAVKKSVFNSEISSWFYKMILLALSTLLFAGLLAWLIWKRIYGPLRKVNLEIIRMAENVTAPVAFTNVAEFDFVLMNFQQMKDQVNELILAVARNEKQKSQFEIEKLLSQINPHFLHNTLNTVQWLARLNGQKEIDKLVTLLVKVLHYNLGKQSIIVTIGEEIEAIRNYMELQRIRYDYEFEFNVQADETVLDAAVPRFLLQPLVENSIYHGLSDNGRVDVIITAHGPGEVQLCVRDSGTGMDEAQIAELLADDGVAGRGLGIGFSYVMRMLRTYYGEQMTLQIHSAANEGTTVSIIIPIKGKEDFDD
>NZ_LN831776.1|WP_020427756.1|5066551_5067949_-|response-regulator
MIKAVVVDDERLVRKGFISLIDWSSFGVVIVGEAGDGNAALTLLREQEADLLFVDLTMPGMSGFELIRQVRQRYPAIRCVVLTCHHEFDYVQEALRLGAVDYIVKTLLEVENADETIRRLVERVKWEDSTRELLARGEGRVMAADVALLYLPQLPDSHEEELFRLSVTKNNPLLAFQNMWMSPLLSRIPDKETCRELQTVLGAGWQAALVSGLKNQLLQEVEEVLGKAVRHALFYYCGAEDPARLEFGELRRIAGERFSAGEDTLSEAQNLRWALDRETWEGFTSGVQQRQPAQEQISAFSHLLLHDWSGLLLKAEEAAQLEASAAGNLNWCHWKSWLRQFSGCVQQRMLELGLSKEVVFCLIRAVRFMKAHAGDKINQGDVATEINMSRGYFSQCFARFAGETFGECLRGMRLELAKTLLLETYYPIGEIAGRSGFEDDRYFSRLFREHVGKLPSEYRAEGMKR
>NZ_LN831776.1|WP_052741504.1|5064857_5066555_-|extracellular-solute-binding-protein
MNRAVRHVLPAVALLCLAACREGNAPAAGSGSADIRAIKAESAAYGRYEEPVVMRIGFKVPDSRLNTGDSNDNNPISRYLESLTNIKVIHSWEAKGEEPFTQKVQLAIDSNDLPDAMVVDRDQLEKLIDSDMIADLTQTYKEFGSELIKDMYDSTQGEALGDATRNGRLYGLPNVAIHADSPSLLWVRQDWLDRVELPAPRSFEDIEAIAKAFIEQDPDGNGKRDTVGLSAYNNIVYGTKPHVNGLDTLFSALHAFPTNWIRDSRGNVVYGSITPETKEALGKLAGWYKRGLIDPDFALYKETQEPIISGKAGMFFGPWWMPYYPLSEAVALDTRAEWRAYAAPLDASGKFVTHMAPVTDRYLVVRKGYEHPEAVVKLLNVFTRLERRRDPNLEAVRSLDDFSAQTGIQPRAYYPFDLLIDYADAIEKHYADMQQALHGKIDPDSLDPDTHLLYDLWLADEEQPKKNLEGWKAANAYKYGVSVLSTTAIDRVRSVFYGSTLHMRSNWPELQKLESETFLNIIVGDSPLSDFDLFAAKWRSLGGDAITQEVAKAVNIRDEDKQGGE
>NZ_LN831776.1|WP_020427758.1|5063464_5064646_+|MFS-transporter
MSLLCLTLGAFAIGMTEFIIMGLLPNVARDLGVSIPQAGQLITSYALGVAIGAPVLTIFTHRLPQKKLLMILMCIFIFGNAVSVIAPTYTLLILARILTAFAHGTFLGVGTIIAARLVRPEKRAGAVSVVLAGLTVANIIGVPFGTFIGQQLGWRASFGAITVLGVVSLFGIIRFIPVIVQEQTANLSEQVRGLLNPKVLLILLTGALGCASLFSLFTYITPMLEEITGFAEHNVTWILVLFGAGVTLGNLIGGKLADWKLMPSLIVNFAILAIMISLFSWTLHNPVLTIINVFMWGIAAFGIMPGIQLRIMNLAHKAPLLATTSSHSALNLGNATGAYLGGAAITQWGLSSIPWLAASLAALGLAGAWLSYLSTRSRQAALTAGDVSATSSS
>NZ_LN831776.1|WP_020427759.1|5062907_5063414_+|YbaK/EbsC-family-protein
MSIANVKEHFRRVGREQDILEFATSSATVEMAAATIGVIPARIAKTLSFRGTDESAILVVAAGDAKVDNKKFRESFGLKARMLSPEEVLEQTGHEIGGVCPFGLARDLEVYLDVSMKRFTTLFPACGSTNSAIELNCDELAVYSGAKDWVDVCKGWNEPLETGEGSAH
>NZ_LN831776.1|WP_020427760.1|5062315_5062750_+|MarR-family-transcriptional-regulator
MLNSNREPIGKLVSQLHRQNQKYLVKELLPYGIGSGGQHIFLKLIVNHPGITQDQMTNEMKFDKATTARSVKKLEEAGYIERRTDPKDRRSSLLYPTPKAVKFAPVLQSILTDLDRKLTLDLDGDEVDQLIALLQKVNKNSAKL
>NZ_LN831776.1|WP_046507248.1|5060688_5062155_-|MFS-transporter
MMSTMTATYQEDAAVQKKRWLILIVLNLFTFMSTLDGSIVNIALPVLVKQLHLPMAQVEWVTTGYLMAICSAVLFFGKLGDIAGKIRIFKIGTVIFILGSLLCGLSASLPLLIASRVIQAIGASMTMANSQGIVTDIFPATERGKALGLIGTFVSLGSIAGPSLGGIIVSTLGWEYIFWVNVPIGLIAIVLGWKVLPKDLIRVKSKIDLPGSLLFAVFIVTLFAGMLLGQQVGYGDSRIISALAAAAAAFIVFLIVELRRSQPLLQLSLFKNPLFSLSILCAFLVFVANFCFNIIAPFYAQNMLNLSPFYAGFLLMLFPISMVIVAPLSGALSDKIGSEFLTFAGLIVMVIAQFGLARLHDGSAVALVGVWIAMLGIGSGLFQSPNNSLIMSTVPRTQLGSAGSVNSLVRNVGMVVGITIATSILFNVMSSKAGYRVTDLIPGRPDVFLSGMHVVFMTSSAICLVSALLTGWRLFSIKRAKRAKRASA
>NZ_LN831776.1|WP_046504623.1|5074447_5075362_-|fumarylacetoacetate-hydrolase-family-protein
MKLMNFWESGNLRLGVKKEEGILDVAAALNALPQRAAGAVPATLREVLDGGEAALDSLRKFADSLPYHDEGAKAFYRDETLLEFAPCTADPGKIICIGLNYRRHAEETGMPLPEYPILFSKFSNSLSGHGMEVPLPYSTQKVDYEAELGIMIGRTAKNVSEEEALDAVFGYFAANDLSARDLQTRTSQWLAGKSCDRFAPVGPYVVTEDEVGDPGLLRISCSVNGEVRQDSNTSDMIFDCRQIISYISSCMTLSPGDIILTGTPEGVMMGYPPEKQVYLQPGDEVTVEIEKLGRLTNRMVAEKA
>NZ_LN831776.1|WP_046507254.1|5075445_5076303_-|SMP-30/gluconolactonase/LRE-family-protein
MLLDAQAELGEGAHWDSEAGRLYWVNIEGRQLRIVDPVTLSEQTHIFGQMISAAVPAVSGGWVVALQDGIYKFQEDQSLELLAHVEKDLPGNRLNDAKCDSKGRLWFGTMSMEDKRDAGSLYVMEPGGEVRKVLSGIGISNGLAWDDSCGLMYYIDTLTRGVDVMDYDLQNGTVSGRRTVVRFPEGAGSPDGMTIDSEGMIWVAHWNGGCVSRWNPHTGEQIGKIEVPAPFVTSCAFGGGHLNELYITSARGSMSPEELQRWPLAGGLFKANTGIRGVPANCFAG
>NZ_LN831776.1|WP_020427748.1|5076495_5077122_+|hypothetical-protein
MKYEWKKQDKAIYFPPAEPVLITVPAYNYFMLQGTGNPNSEEFAQAVGVLYSLTYAIKMLPKKGPAPEGYHEYSIFPLEGVWDLSEKGRSQAALDKNELVYTIMIRQPEFVTPDLAGSIMEKVQRTKPHPLLQKAVFGSSEDGPSVQMLHTGPYDEEPASFRKMEQYCAEHGLRRLSKTHREIYLTDARRTQPEKQKTVLRFLVAEET
>NZ_LN831776.1|WP_020427747.1|5077168_5078704_-|MFS-transporter
MSSAQKSPKLGIVIAGLLLGILMASMDSTIVATAMGNIVGELGGMDKFVWVTSAYLVAEMTGMPIFGKLSDMYGRKKFFIFGIIVFMAGSALCGTADTITQLAAYRALQGIGGGALVPIAFAIMFDAVPLETRGKLGGAFGAVFGLSSIFGPLLGAYITDHIAWQWVFYINLPLGVIALVMVVSFYRESVEHSKHPIDWLGAGTLLGAVISLMFALELGGKEYAWDSGLILGLFAAFAVLAVLFMFAETKAKEPIISFALFRQRLYASSILCALFSGAAFIAASVYIPIFIQGVLGGSATNSGLVLLPMMVASVVTASTGGFLMVKTSYRSLMVPTLILLVLGTGLVATLEPDASRLLVTFYMILIGLGVGASFSVLSTAAIHGLTPQQRGSASATLNFIRSLGMTIGITAFGIIQSHYFSSKLTQVFPGTAGAAPGGAMNFKDPHALLSPETRAQIPPGILSKITDGLSFSITSTFAWAAVPALLALLAACFMGRQKMDASAEGQMPSGH
>NZ_LN831776.1|WP_052741505.1|5078822_5079491_-|hypothetical-protein
MNETANRTNLKILGNSTSAGGRFLDVKVTGECTFHGDVDCRKLTLMGETKVSGSLVMESMKLTGECSVKGGIEGESLRGQGEIRAECVHVEGIKFTGNLSVSGNCDAEDMQISGAVQIDGLLSAETLELSLFGPSRAAEVGGGSIKIKRSLGGALIRPGHPGQLRFAAGLIEGDHVDLQNTAADTVRGGRVVIGSGCEIGTVEYRDFLDIHPNAVVRNQVKV
>NZ_LN831776.1|WP_141639074.1|5079483_5080173_-|hypothetical-protein
MMDKGAAADLLIAGIGGAAGGTYNHVSLEGLSRINGPVTAMTFTGNGRMKVGGSLTVEQMETNGDLKIGGGLRIGTMKHDGLLKIDGGLLGESFTLNGVADIKGDCELEKFTAEGVVTIGGFLSAGCVELVLQGQAKVKELGVESLVIRKGGSGVWNKLAGGIIPKLRPELQAKVIEGDFLDLEYTTAEVVRGAVIIIGEGCSIGRVEYRDRLTVHPGASVGMEEKTGE
>NZ_LN831776.1|WP_020427743.1|5080250_5080880_-|YhbD-family-protein
MEEDLISKKELLDLTGISYGQLYRWKRKQLIPESWFIRKSTYTGQETFFPKERMLGRIQHILSKKDDLSLDELAGKLSDMSSVHKQWLTIEEVRERNIVSSITLERYGQCDRDEHKYSFEQLIHLVAVDLLLGKGELSLEEADLLHRTLSMNRTQFGGKRWELFFARKMGVSFFLQAQAPSELVFDEGVRLISRITLEDLTEQLQGKLG
>NZ_LN831776.1|WP_046504625.1|5081069_5082206_-|GNAT-family-N-acetyltransferase
MGDIRFVSREELKQAAELSDLVFRDEEQTSMAVKFPGIFSGSYLSSPGVFEDGQLVAFAGLVPGFIQMGTVSVPVFSLGSVCTHPEYRGKGYANALLQRVFDHIDRAGASLLLVSGTRDLYIRQGCHTFRSVRSYLLSPENEVVRRAAAGPAIVREAEERDWFGLQRLAENREVRYDRSLYELATLVRAEAIADIYKLKQKIYVAESDGRLLAYAVIAVRNKLKTEAVPLVIEWGGAPEAALQAVSQVIAAKGISELQFQVPWHETGMIRALGSSTYLEEPNPGTVKIVNPVRLWQQIHPYLQQKSPEALSGVELHSAAPGGETVLTVNGTAVHLSDMELISLFFDTQPQLELPVAIREQLKELFPVPLPYASGLNFV
>NZ_LN831776.1|WP_046504627.1|5082339_5083689_-|tellurium-resistance-protein-TerF
MDGTIINLVSGSNAKLDEVSMNARVKISCSSSPAELDLSCFMVGADGRVPADDYFIFYNQPADPQRAVRFEPIDKYSGEFVIDLRALQSSGVEKCVFAATLDGPGTFAEVRGCKISAAAGNTELVFAITEGKAETSLVLAELYRHGQGFKLRAVGRGFHGGLKPLAEAHGVEVEDEPAAEAASPGEPGHTAAAAAELSASIAEAAAATAATPPAQPDPPLKLNLTKIDLHKQQVALSLRKKNIEQEKARVAVVFDASGSMSALYQKGVVQRAFERVLAVAASMDDDGMLDVWFFATKSKRMPSVRETGYEDYVKRTYPGPRMFGGLGIGNNEPVVMADILKKYTKEDPGILPVYVVFFSDGGIYETRKISKLLIDSSKHNIFWQFVGLGQADYGVLRELDDLQGRYVDNADFFALDDLDEVSDEELYDRLFNEFPKWLREAREKGVIRS
>NZ_LN831776.1|WP_020427739.1|5083837_5084452_-|50S-ribosomal-protein-L25
MNTTVRLTERSGSTSSQRSKGFVPVVVYGAGSDSQSFTADAKTLNEILGKNPRAILKVELPGSGSKNVVIQEVQRQPLSRKLLHVDLHQIDMKAELDTKVAFHFTGDPVGVKSGGIQQVELYELDIRTLPDKLTATFEVDISGLDVGDQLLVSDLPKHEGWEVLTPEDTLIVRIAPPVALEEPAGAEADEPAAAEAAEEQKTEE

Crispr_ID: NZ_LN831776_51

• CRISPR_ID: NZ_LN831776_51
• CRISPR_location: 5084468-5084566
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_51

Consensus_repeat	Method
AAGTTTTGTCAGCTTAGCTGCATTGAATAGTTC	CRISPRCasFinder

spacers of NZ_LN831776_51

>51.1|5084501|33|NZ_LN831776|CRISPRCasFinder
TTCGTACAAAACTGGCTTCGGAAGCATACGCTT

CRISPR arrays and Neighbor proteins around NZ_LN831776_51

CRISPR arrays

The CRISPR arrays of NZ_LN831776_51

>merge|NZ_LN831776|51|5084468-5084566|CRISPRCasFinder
AAGTTTTGTCAGCTTAGCTGCATTGAATAGTTCTTCGTACAAAACTGGCTTCGGAAGCATACGCTTAAGTTTTGTCAGCTCAGCTGCATTGAATAGTTC

>NZ_LN831776|51|52|5084468-5084566|CRISPRCasFinder
AAGTTTTGTCAGCTTAGCTGCATTGAATAGTTC	TTCGTACAAAACTGGCTTCGGAAGCATACGCTT
AAGTTTTGTCAGCTCAGCTGCATTGAATAGTTC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020427731.1|5091942_5092224_+|N-acetyltransferase	unknown	unknown	gnl|CDD|379642
NZ_LN831776.1|WP_141639074.1|5079483_5080173_-|hypothetical-protein	unknown	unknown	gnl|CDD|224578
NZ_LN831776.1|WP_046504627.1|5082339_5083689_-|tellurium-resistance-protein-TerF	unknown	unknown	gnl|CDD|378410
NZ_LN831776.1|WP_020429140.1|5095642_5096011_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224647
NZ_LN831776.1|WP_046504623.1|5074447_5075362_-|fumarylacetoacetate-hydrolase-family-protein	unknown	unknown	gnl|CDD|223257
NZ_LN831776.1|WP_046504625.1|5081069_5082206_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379240
NZ_LN831776.1|WP_020427739.1|5083837_5084452_-|50S-ribosomal-protein-L25	unknown	unknown	gnl|CDD|235534
NZ_LN831776.1|WP_020427729.1|5093396_5094467_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|187652
NZ_LN831776.1|WP_046507254.1|5075445_5076303_-|SMP-30/gluconolactonase/LRE-family-protein	unknown	unknown	gnl|CDD|369882
NZ_LN831776.1|WP_020427736.1|5086888_5087812_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|224094
NZ_LN831776.1|WP_020427732.1|5090827_5091730_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|238042
NZ_LN831776.1|WP_020427743.1|5080250_5080880_-|YhbD-family-protein	unknown	unknown	gnl|CDD|379048
NZ_LN831776.1|WP_052741505.1|5078822_5079491_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427737.1|5085890_5086874_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|223521
NZ_LN831776.1|WP_020427748.1|5076495_5077122_+|hypothetical-protein	unknown	unknown	gnl|CDD|227169
NZ_LN831776.1|WP_020427730.1|5092267_5093119_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831776.1|WP_046504632.1|5088841_5090596_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|173853
NZ_LN831776.1|WP_046504629.1|5087827_5088781_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|223674
NZ_LN831776.1|WP_020427747.1|5077168_5078704_-|MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_LN831776.1|WP_020427738.1|5084932_5085898_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|236898

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020427731.1|5091942_5092224_+|N-acetyltransferase	gnl|CDD|379642	pfam14542, Acetyltransf_CG, GCN5-related N-acetyl-transferase. This family of GCN5-related N-acetyl-transferases bind both CoA and acetyl-CoA. They are characterized by highly conserved glycine, a cysteine residue in the acetyl-CoA binding site near the acetyl group, their small size compared with other GNATs and a lack of of an obvious substrate-binding site. It is proposed that they transfer an acetyl group from acetyl-CoA to one or more unidentified aliphatic amines via an acetyl (cysteine) enzyme intermediate. The substrate might be another macromolecule.	9.65056e-31
NZ_LN831776.1|WP_141639074.1|5079483_5080173_-|hypothetical-protein	gnl|CDD|224578	COG1664, CcmA, Integral membrane protein CcmA involved in cell shape determination [Cell envelope biogenesis, outer membrane].	0.0012075
NZ_LN831776.1|WP_046504632.1|5088841_5090596_-|ABC-transporter-substrate-binding-protein	gnl|CDD|173853	cd00995, PBP2_NikA_DppA_OppA_like, The substrate-binding domain of an ABC-type nickel/oligopeptide-like import system contains the type 2 periplasmic binding fold. This family represents the periplasmic substrate-binding domain of nickel/dipeptide/oligopeptide transport systems, which function in the import of nickel and peptides, and other closely related proteins. The oligopeptide-binding protein OppA is a periplasmic component of an ATP-binding cassette (ABC) transport system OppABCDEF consisting of five subunits: two homologous integral membrane proteins OppB and OppF that form the translocation pore; two homologous nucleotide-binding domains OppD and OppF that drive the transport process through binding and hydrolysis of ATP; and the substrate-binding protein or receptor OppA that determines the substrate specificity of the transport system. The dipeptide (DppA) and oligopeptide (OppA) binding proteins differ in several ways. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Similar to the ABC-type dipeptide and oligopeptide import systems, nickel transporter is comprised of five subunits NikABCDE: the two pore-forming integral inner membrane proteins NikB and NikC; the two inner membrane-associated proteins with ATPase activity NikD and NikE; and the periplasmic nickel binding NikA, which is the initial nickel receptor that controls the chemotactic response away from nickel. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand binding domains of ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	1.74069e-123
NZ_LN831776.1|WP_046504627.1|5082339_5083689_-|tellurium-resistance-protein-TerF	gnl|CDD|378410	pfam10138, vWA-TerF-like, vWA found in TerF C-terminus. vWA domain fused to TerD domain typified by the TerF protein. Some times found as solos.	3.2817e-97
NZ_LN831776.1|WP_020429140.1|5095642_5096011_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	3.79505e-41
NZ_LN831776.1|WP_046504623.1|5074447_5075362_-|fumarylacetoacetate-hydrolase-family-protein	gnl|CDD|223257	COG0179, MhpD, 2-keto-4-pentenoate hydratase/2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) [Secondary metabolites biosynthesis, transport, and catabolism].	5.83257e-102
NZ_LN831776.1|WP_046504625.1|5081069_5082206_-|GNAT-family-N-acetyltransferase	gnl|CDD|379240	pfam13527, Acetyltransf_9, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	2.06798e-13
NZ_LN831776.1|WP_020427737.1|5085890_5086874_-|ABC-transporter-ATP-binding-protein	gnl|CDD|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.89432e-173
NZ_LN831776.1|WP_020427729.1|5093396_5094467_+|SDR-family-oxidoreductase	gnl|CDD|187652	cd08948, 5beta-POR_like_SDR_a, progesterone 5-beta-reductase-like proteins (5beta-POR), atypical (a) SDRs. 5beta-POR catalyzes the reduction of progesterone to 5beta-pregnane-3,20-dione in Digitalis plants. This subgroup of atypical-extended SDRs, shares the structure of an extended SDR, but has a different glycine-rich nucleotide binding motif (GXXGXXG) and lacks the YXXXK active site motif of classical and extended SDRs. Tyr-179 and Lys 147 are present in the active site, but not in the usual SDR configuration. Given these differences, it has been proposed that this subfamily represents a new SDR class. Other atypical SDRs include biliverdin IX beta reductase (BVR-B,aka flavin reductase), NMRa (a negative transcriptional regulator of various fungi), phenylcoumaran benzylic ether and pinoresinol-lariciresinol reductases, phenylpropene synthases, eugenol synthase, triphenylmethane reductase, isoflavone reductases, and others. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. In addition to the Rossmann fold core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	1.19898e-133
NZ_LN831776.1|WP_046507254.1|5075445_5076303_-|SMP-30/gluconolactonase/LRE-family-protein	gnl|CDD|369882	pfam08450, SGL, SMP-30/Gluconolaconase/LRE-like region. This family describes a region that is found in proteins expressed by a variety of eukaryotic and prokaryotic species. These proteins include various enzymes, such as senescence marker protein 30 (SMP-30), gluconolactonase and luciferin-regenerating enzyme (LRE). SMP-30 is known to hydrolyze diisopropyl phosphorofluoridate in the liver, and has been noted as having sequence similarity, in the region described in this family, with PON1 and LRE.	2.1488e-92
NZ_LN831776.1|WP_020427747.1|5077168_5078704_-|MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	2.72902e-69
NZ_LN831776.1|WP_020427732.1|5090827_5091730_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|238042	cd00090, HTH_ARSR, Arsenical Resistance Operon Repressor and similar prokaryotic, metal regulated homodimeric repressors. ARSR subfamily of helix-turn-helix bacterial transcription regulatory proteins (winged helix topology). Includes several proteins that appear to dissociate from DNA in the presence of metal ions.	1.11621e-07
NZ_LN831776.1|WP_020427743.1|5080250_5080880_-|YhbD-family-protein	gnl|CDD|379048	pfam13171, DUF4004, Protein of unknown function (DUF4004). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are approximately 210 amino acids in length.	1.51022e-82
NZ_LN831776.1|WP_020427748.1|5076495_5077122_+|hypothetical-protein	gnl|CDD|227169	COG4832, COG4832, Uncharacterized conserved protein [Function unknown].	8.93154e-65
NZ_LN831776.1|WP_020427730.1|5092267_5093119_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	3.35035e-12
NZ_LN831776.1|WP_020427736.1|5086888_5087812_-|ABC-transporter-permease	gnl|CDD|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	6.02167e-97
NZ_LN831776.1|WP_046504629.1|5087827_5088781_-|ABC-transporter-permease	gnl|CDD|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.30283e-116
NZ_LN831776.1|WP_020427739.1|5083837_5084452_-|50S-ribosomal-protein-L25	gnl|CDD|235534	PRK05618, PRK05618, 50S ribosomal protein L25/general stress protein Ctc; Reviewed.	3.56076e-48
NZ_LN831776.1|WP_020427738.1|5084932_5085898_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|236898	PRK11308, dppF, dipeptide transporter ATP-binding subunit; Provisional.	9.64096e-143

Protein sequences

>NZ_LN831776.1|WP_020427739.1|5083837_5084452_-|50S-ribosomal-protein-L25
MNTTVRLTERSGSTSSQRSKGFVPVVVYGAGSDSQSFTADAKTLNEILGKNPRAILKVELPGSGSKNVVIQEVQRQPLSRKLLHVDLHQIDMKAELDTKVAFHFTGDPVGVKSGGIQQVELYELDIRTLPDKLTATFEVDISGLDVGDQLLVSDLPKHEGWEVLTPEDTLIVRIAPPVALEEPAGAEADEPAAAEAAEEQKTEE
>NZ_LN831776.1|WP_046504627.1|5082339_5083689_-|tellurium-resistance-protein-TerF
MDGTIINLVSGSNAKLDEVSMNARVKISCSSSPAELDLSCFMVGADGRVPADDYFIFYNQPADPQRAVRFEPIDKYSGEFVIDLRALQSSGVEKCVFAATLDGPGTFAEVRGCKISAAAGNTELVFAITEGKAETSLVLAELYRHGQGFKLRAVGRGFHGGLKPLAEAHGVEVEDEPAAEAASPGEPGHTAAAAAELSASIAEAAAATAATPPAQPDPPLKLNLTKIDLHKQQVALSLRKKNIEQEKARVAVVFDASGSMSALYQKGVVQRAFERVLAVAASMDDDGMLDVWFFATKSKRMPSVRETGYEDYVKRTYPGPRMFGGLGIGNNEPVVMADILKKYTKEDPGILPVYVVFFSDGGIYETRKISKLLIDSSKHNIFWQFVGLGQADYGVLRELDDLQGRYVDNADFFALDDLDEVSDEELYDRLFNEFPKWLREAREKGVIRS
>NZ_LN831776.1|WP_046504625.1|5081069_5082206_-|GNAT-family-N-acetyltransferase
MGDIRFVSREELKQAAELSDLVFRDEEQTSMAVKFPGIFSGSYLSSPGVFEDGQLVAFAGLVPGFIQMGTVSVPVFSLGSVCTHPEYRGKGYANALLQRVFDHIDRAGASLLLVSGTRDLYIRQGCHTFRSVRSYLLSPENEVVRRAAAGPAIVREAEERDWFGLQRLAENREVRYDRSLYELATLVRAEAIADIYKLKQKIYVAESDGRLLAYAVIAVRNKLKTEAVPLVIEWGGAPEAALQAVSQVIAAKGISELQFQVPWHETGMIRALGSSTYLEEPNPGTVKIVNPVRLWQQIHPYLQQKSPEALSGVELHSAAPGGETVLTVNGTAVHLSDMELISLFFDTQPQLELPVAIREQLKELFPVPLPYASGLNFV
>NZ_LN831776.1|WP_020427743.1|5080250_5080880_-|YhbD-family-protein
MEEDLISKKELLDLTGISYGQLYRWKRKQLIPESWFIRKSTYTGQETFFPKERMLGRIQHILSKKDDLSLDELAGKLSDMSSVHKQWLTIEEVRERNIVSSITLERYGQCDRDEHKYSFEQLIHLVAVDLLLGKGELSLEEADLLHRTLSMNRTQFGGKRWELFFARKMGVSFFLQAQAPSELVFDEGVRLISRITLEDLTEQLQGKLG
>NZ_LN831776.1|WP_141639074.1|5079483_5080173_-|hypothetical-protein
MMDKGAAADLLIAGIGGAAGGTYNHVSLEGLSRINGPVTAMTFTGNGRMKVGGSLTVEQMETNGDLKIGGGLRIGTMKHDGLLKIDGGLLGESFTLNGVADIKGDCELEKFTAEGVVTIGGFLSAGCVELVLQGQAKVKELGVESLVIRKGGSGVWNKLAGGIIPKLRPELQAKVIEGDFLDLEYTTAEVVRGAVIIIGEGCSIGRVEYRDRLTVHPGASVGMEEKTGE
>NZ_LN831776.1|WP_052741505.1|5078822_5079491_-|hypothetical-protein
MNETANRTNLKILGNSTSAGGRFLDVKVTGECTFHGDVDCRKLTLMGETKVSGSLVMESMKLTGECSVKGGIEGESLRGQGEIRAECVHVEGIKFTGNLSVSGNCDAEDMQISGAVQIDGLLSAETLELSLFGPSRAAEVGGGSIKIKRSLGGALIRPGHPGQLRFAAGLIEGDHVDLQNTAADTVRGGRVVIGSGCEIGTVEYRDFLDIHPNAVVRNQVKV
>NZ_LN831776.1|WP_020427747.1|5077168_5078704_-|MFS-transporter
MSSAQKSPKLGIVIAGLLLGILMASMDSTIVATAMGNIVGELGGMDKFVWVTSAYLVAEMTGMPIFGKLSDMYGRKKFFIFGIIVFMAGSALCGTADTITQLAAYRALQGIGGGALVPIAFAIMFDAVPLETRGKLGGAFGAVFGLSSIFGPLLGAYITDHIAWQWVFYINLPLGVIALVMVVSFYRESVEHSKHPIDWLGAGTLLGAVISLMFALELGGKEYAWDSGLILGLFAAFAVLAVLFMFAETKAKEPIISFALFRQRLYASSILCALFSGAAFIAASVYIPIFIQGVLGGSATNSGLVLLPMMVASVVTASTGGFLMVKTSYRSLMVPTLILLVLGTGLVATLEPDASRLLVTFYMILIGLGVGASFSVLSTAAIHGLTPQQRGSASATLNFIRSLGMTIGITAFGIIQSHYFSSKLTQVFPGTAGAAPGGAMNFKDPHALLSPETRAQIPPGILSKITDGLSFSITSTFAWAAVPALLALLAACFMGRQKMDASAEGQMPSGH
>NZ_LN831776.1|WP_020427748.1|5076495_5077122_+|hypothetical-protein
MKYEWKKQDKAIYFPPAEPVLITVPAYNYFMLQGTGNPNSEEFAQAVGVLYSLTYAIKMLPKKGPAPEGYHEYSIFPLEGVWDLSEKGRSQAALDKNELVYTIMIRQPEFVTPDLAGSIMEKVQRTKPHPLLQKAVFGSSEDGPSVQMLHTGPYDEEPASFRKMEQYCAEHGLRRLSKTHREIYLTDARRTQPEKQKTVLRFLVAEET
>NZ_LN831776.1|WP_046507254.1|5075445_5076303_-|SMP-30/gluconolactonase/LRE-family-protein
MLLDAQAELGEGAHWDSEAGRLYWVNIEGRQLRIVDPVTLSEQTHIFGQMISAAVPAVSGGWVVALQDGIYKFQEDQSLELLAHVEKDLPGNRLNDAKCDSKGRLWFGTMSMEDKRDAGSLYVMEPGGEVRKVLSGIGISNGLAWDDSCGLMYYIDTLTRGVDVMDYDLQNGTVSGRRTVVRFPEGAGSPDGMTIDSEGMIWVAHWNGGCVSRWNPHTGEQIGKIEVPAPFVTSCAFGGGHLNELYITSARGSMSPEELQRWPLAGGLFKANTGIRGVPANCFAG
>NZ_LN831776.1|WP_046504623.1|5074447_5075362_-|fumarylacetoacetate-hydrolase-family-protein
MKLMNFWESGNLRLGVKKEEGILDVAAALNALPQRAAGAVPATLREVLDGGEAALDSLRKFADSLPYHDEGAKAFYRDETLLEFAPCTADPGKIICIGLNYRRHAEETGMPLPEYPILFSKFSNSLSGHGMEVPLPYSTQKVDYEAELGIMIGRTAKNVSEEEALDAVFGYFAANDLSARDLQTRTSQWLAGKSCDRFAPVGPYVVTEDEVGDPGLLRISCSVNGEVRQDSNTSDMIFDCRQIISYISSCMTLSPGDIILTGTPEGVMMGYPPEKQVYLQPGDEVTVEIEKLGRLTNRMVAEKA
>NZ_LN831776.1|WP_020427738.1|5084932_5085898_-|ATP-binding-cassette-domain-containing-protein
MSEALLEVSHLKKYFPVTEGLLNRTVGHVKAVDDISLTLQPGETFGLVGESGSGKSTVGRTILRLTEKTAGEVKFKGVDIHSLSPAELRLLRPRMQLIFQDPYSALNPRVRVGDAIGEALLDHGLCTKDEVRELVLESLAACGLSYYHIDRFPHEFSGGQRQRIGIARALILNPDLIIADEPVSALDVSIQAQIINLFSKLQQSKGLAYLFISHDLSVVEHLCSRIGVMYLGSMVETAARDELFHNPLHPYTKALLSAVPVPVPRLKRERIVLKGDIPSPANPPSGCKFHTRCPFAVEVCKAENPVFRDAGGGHFVACHLV
>NZ_LN831776.1|WP_020427737.1|5085890_5086874_-|ABC-transporter-ATP-binding-protein
MKHLMKIEGLSTVFHTEEGKVTAVDKVSFQVREGETVCIVGESGCGKSVTAMSIMGLVEAPGGQVNGGRIDFAGEDLLRLDKNTLRAIRGNEIAMIFQEPMSSLNPVMKIGEQIMEPLMVHLKLSKKQARIRAVELITQVGIARPEQIFGSYPHELSGGMLQRIMIAIAVSCNPKLLIADEPTTALDVTIQAQILDMLREFKENSGMSILLITHDLGVVAEMADYVIVMYSGQIVEEGGVVELFNHPKHPYTRGLLKSKPVVGQRLEELYSIPGQVPNPLMLEQSCYFHDRCEHCMPVCRSRQPRLKELDGGQKTACWLYEEAEVHV
>NZ_LN831776.1|WP_020427736.1|5086888_5087812_-|ABC-transporter-permease
MTVNSRLAGLREPQVQRQKSSLFRQSLKRLMKNRLAVAGFGVVVFMFALCFIGPFFSPYADNKINMAMMNKAPSLQHLLGTDALGRDILTRVMQAGRISLTVGLASMVLSVFIGALLGAVAGYYRGIADQIIMRIADLLMTIPGLPLLFIFGALLSEWKVPTDYRMYIVMLMLSIVNWPGLARMVRGQMLSLREREFMQAAVVLGLRDSRKLFHHLLPNVVPLLIVMATLNIGGAILSESVLSFFGLGVMPPTPTWGNMIDAANNMIDFQDHPWLWIPPGLSIFATVIAINIFGDGLRDVLDPKQKR
>NZ_LN831776.1|WP_046504629.1|5087827_5088781_-|ABC-transporter-permease
MSTYLTKRLLYMLIILFAASLLIFILYASTPGDFITGNIKLTAERKAELREIYGLNKPVLERYGTWMNNAFHGDFGYSLAQQKPVLQLFNDYIWNSFLLAAVSTFLTWVIAVIVGVISAYKQYSWFDTLVMVAIFAAMSLPSFFIGLFLIKILAVDLKWLPPGGMITTGSHATGLAYLKEVVRHMALPVVVMTLLGLGSLTRYFRSNMIDVLKQDYIRTARAKGLKERKVLFRHALRNALLPAITLVGFELPALFGGSLIIEQIFNWPGIGQLYMKSFGLRDYPLLMGFTMFIAILTVIGTLLSDILYRVADPRVRL
>NZ_LN831776.1|WP_046504632.1|5088841_5090596_-|ABC-transporter-substrate-binding-protein
MRKSTLVLSTLLIAGSLLLTACSDNSSNSATGNAPASATSDPGTTGTEASASPAPVPAGALSEPFTAADLSKLPAVAQNRNDTIIVGLTDPSGAFTPYFQESGYDGNVSSLLYASLVTVDDKGVPTPELAESWDVSDDQLTYTFHLRKDLKFSDGSPLTADDVAFTWTIQYDKAYDGGSSVPSMNVKGGKAYKEGTAKTIEGIKVIDPQTISVTLEKPNATALVTLGSNVLSKAYYGKDYTFGHLEYIKKLHEHPLGDGPYKLEKFLPGQEVRFTANENYFKGKPKTEHFIYKTSEGDVWQFLETGEVDYASFSATDENIEKLKALGFVNILPYTPSTYGYMQVNLKHEQLKDKEVRQAIMYGLDRQSIYVDAAQGAGSIANIPASPISWAYTEEGINPYKYDPEKAKQLLDQAGWTVGANGIREKAGKPLTIHYLGSKSKNTDIFIAVAKENFEALGIEFQPEVFADFNSLVSKVEGGDYDLVSFSTSMLTDPADGFMQFFDGEITDYDNPKFLELYNKALATTDIEQRKAVYKELYQLFNDELPILFTSYKKTVYAYNGRIQNLTVSPFIGLAGSLPEWTLK
>NZ_LN831776.1|WP_020427732.1|5090827_5091730_-|helix-turn-helix-transcriptional-regulator
MEYEVEVQFEPVYELVSSIHTFICKKSNKKMDLGTSWSAEVAGKLSPELLSALEETELGNDWKLLNLLIYQCPVKDSVDTALEWLERLPVGEMYETLSEYISVFPVQMDQFRSRMHFLLSEWNRQYFRGTSPEIIGKLRQHTEEQRLEADNRAVSDFVNRTTNGFYFLPGDGLRKLVLIPQFHFQPANIIYSFGPLTICHYAARISVADEEISPSMYRTLRSLGEKSRLKILQSLGGGRKTFTEIARQAGISKGIVHDHIFSLRCAGLLHAYIEGENVIAYSLRLEGIRRMNEQLFEYLQ
>NZ_LN831776.1|WP_020427731.1|5091942_5092224_+|N-acetyltransferase
MESIEQGEGRFYIAGDGKDLAEITYRTDETTGNWVIDHTFVSEDLRGQGAGEKLVRAVVDKARAEQVKIVPQCPYAAHQFKKHEEYGDVLSRS
>NZ_LN831776.1|WP_020427730.1|5092267_5093119_+|GNAT-family-N-acetyltransferase
MNTAEMLKDIEELQQRCEQYEGISLKLNWDMLRLSPEAGGAEWLVTYEEDVLAGFIGLYGIAGEMEVCGMVRPGFRRRGIFTSLWEQAQSIIKRNQIRTLLLNAPASSASAAGFLKTLPVVFNHAEYQMKWDGSAVPQGSPEASSAAGAVVLRPARQDEADLLVELDCSGFDMSKEDAAEMYTQQMNENQQEQIIIEMNGQPAGKMRLWTEDNETWIYGFTVDKKLRGLGIGRSALLQTIEREQRNYNGVNLEVALDNPNALRLYESCGFVILNKQDYYRYTG
>NZ_LN831776.1|WP_020427729.1|5093396_5094467_+|SDR-family-oxidoreductase
MNPNDAVQRKTALVIGANGVIGRNLIGHLATLPEWDIIGVSRRGGVNTSRVRYIAADLLDAEETRLKLGTLPEVTHIFYAAYQERPTWAELVPPNLAMLVNAVEAVEPVARNLQHISLMQGYKVYGAHLGPFKTPARETDANHMPPEFNIDQQNFLEQRQIGKTWTWSAMRPSVVCGFALGNPMNLAMVIAVYASISKELGLPLRFPGKPGAYHSLLEMTDAGLLAQATVWAATDSRCANQAFNITNGDLFRWDELWPKLAAFFGLETAPPLPMSLSVVMEDKEALWNGMVEKYSLEPNSYRDVSSWGFGDFVFSWDYDFFADGSKARRFGFHEFIDTEAMFMNIFTDLRSRKVIP
>NZ_LN831776.1|WP_020429140.1|5095642_5096011_-|helix-turn-helix-transcriptional-regulator
MPEPIKTYNTAVEATLEVIGGKWKPVILFFLTFGKKRNGEFISLMPVITQKVLTQQLRELEEDGVIKRTVYNEVPPRVEYELTDYGWSLKEILHLMCRWGDAHIERVYGDQAAVLAQPQTKA

Crispr_ID: NZ_LN831776_52

• CRISPR_ID: NZ_LN831776_52
• CRISPR_location: 5129839-5129913
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: csa3

Consensus repeat of NZ_LN831776_52

Consensus_repeat	Method
AAGTGGAAAAAGGGACACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_52

>52.1|5129862|29|NZ_LN831776|CRISPRCasFinder
TGCCGGAGTAACCTATCTTCGGGCAGATG

CRISPR arrays and Neighbor proteins around NZ_LN831776_52

CRISPR arrays

The CRISPR arrays of NZ_LN831776_52

>merge|NZ_LN831776|52|5129839-5129913|CRISPRCasFinder
AAGTGGAAAAAGGGACACTAATTTGCCGGAGTAACCTATCTTCGGGCAGATGAAGTGGAAAAAGGGACACTAATT

>NZ_LN831776|52|53|5129839-5129913|CRISPRCasFinder
AAGTGGAAAAAGGGACACTAATT	TGCCGGAGTAACCTATCTTCGGGCAGATG
AAGTGGAAAAAGGGACACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020431263.1|5120797_5122447_-|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_020431264.1|5118970_5120794_-|histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_020431267.1|5114899_5116411_-|sugar-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224053
NZ_LN831776.1|WP_020432793.1|5132264_5132531_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020432802.1|5141198_5142623_-|3-isopropylmalate-dehydratase-large-subunit	unknown	unknown	gnl|CDD|235490
NZ_LN831776.1|WP_046504662.1|5123530_5124721_-|formate-dependent-phosphoribosylglycinamide-formyltransferase	unknown	unknown	gnl|CDD|236454
NZ_LN831776.1|WP_020431266.1|5116534_5117614_-|galactose/glucose-ABC-transporter-substrate-binding-protein-MglB	unknown	unknown	gnl|CDD|380481
NZ_LN831776.1|WP_020432803.1|5142858_5143317_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020432794.1|5132575_5133247_-|endonuclease-III	unknown	unknown	gnl|CDD|223255
NZ_LN831776.1|WP_046504672.1|5138819_5140391_-|AMIN-domain-containing-protein	unknown	unknown	gnl|CDD|119407
NZ_LN831776.1|WP_020432804.1|5143444_5144356_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|176102
NZ_LN831776.1|WP_020431261.1|5123076_5123541_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831776.1|WP_020432798.1|5137217_5138657_-|AMIN-domain-containing-protein	unknown	unknown	gnl|CDD|119407
NZ_LN831776.1|WP_046504665.1|5133386_5136140_-|hypothetical-protein	unknown	unknown	gnl|CDD|306825
NZ_LN831776.1|WP_020428419.1|5128911_5129337_+|SRPBCC-domain-containing-protein	unknown	unknown	gnl|CDD|176856
NZ_LN831776.1|WP_046504674.1|5140568_5141171_-|3-isopropylmalate-dehydratase-small-subunit	unknown	unknown	gnl|CDD|179314
NZ_LN831776.1|WP_046504668.1|5136443_5137109_-|GerMN-domain-containing-protein	unknown	unknown	gnl|CDD|378464
NZ_LN831776.1|WP_046504658.1|5117954_5118974_-|substrate-binding-domain-containing-protein	unknown	unknown	gnl|CDD|380661
NZ_LN831776.1|WP_020428420.1|5129340_5129673_+|winged-helix-turn-helix-transcriptional-regulator	csa3	COG0640_csa3_CAS-I-A	gnl|CDD|238042
NZ_LN831776.1|WP_144412128.1|5124868_5128537_-|dynamin	unknown	unknown	gnl|CDD|206739

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831776.1|WP_020428420.1|5129340_5129673_+|winged-helix-turn-helix-transcriptional-regulator	csa3	COG0640_csa3_CAS-I-A	1.2e-15	52.6	0.1

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020431263.1|5120797_5122447_-|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	1.74301e-56
NZ_LN831776.1|WP_020431264.1|5118970_5120794_-|histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	1.29882e-63
NZ_LN831776.1|WP_020431267.1|5114899_5116411_-|sugar-ABC-transporter-ATP-binding-protein	gnl|CDD|224053	COG1129, MglA, ABC-type sugar transport system, ATPase component [Carbohydrate transport and metabolism].	0
NZ_LN831776.1|WP_020432802.1|5141198_5142623_-|3-isopropylmalate-dehydratase-large-subunit	gnl|CDD|235490	PRK05478, PRK05478, 3-isopropylmalate dehydratase large subunit.	0
NZ_LN831776.1|WP_046504662.1|5123530_5124721_-|formate-dependent-phosphoribosylglycinamide-formyltransferase	gnl|CDD|236454	PRK09288, purT, formate-dependent phosphoribosylglycinamide formyltransferase.	0
NZ_LN831776.1|WP_020431266.1|5116534_5117614_-|galactose/glucose-ABC-transporter-substrate-binding-protein-MglB	gnl|CDD|380481	cd01539, PBP1_GGBP, periplasmic glucose/galactose-binding protein (GGBP) involved in chemotaxis towards, and active transport of, glucose and galactose in various bacterial species. Periplasmic glucose/galactose-binding protein (GGBP) involved in chemotaxis towards, and active transport of, glucose and galactose in various bacterial species. GGBP is a member of the pentose/hexose sugar-binding protein family of the type 1 periplasmic binding protein superfamily which consists of two alpha/beta globular domains connected by a three-stranded hinge. This Venus flytrap-like domain undergoes transition from an open to a closed conformational state upon ligand binding. Moreover, the periplasmic GGBP is homologous to the ligand-binding domain of eukaryotic receptors such as glutamate receptor (GluR) and DNA-binding transcriptional repressors such as LacI and GalR.	1.83481e-153
NZ_LN831776.1|WP_020432794.1|5132575_5133247_-|endonuclease-III	gnl|CDD|223255	COG0177, Nth, Predicted EndoIII-related endonuclease [DNA replication, recombination, and repair].	8.36784e-108
NZ_LN831776.1|WP_046504672.1|5138819_5140391_-|AMIN-domain-containing-protein	gnl|CDD|119407	cd02696, MurNAc-LAA, N-acetylmuramoyl-L-alanine amidase or MurNAc-LAA (also known as peptidoglycan aminohydrolase, NAMLA amidase, NAMLAA, Amidase 3, and peptidoglycan amidase; EC 3.5.1.28) is an autolysin that hydrolyzes the amide bond between N-acetylmuramoyl and L-amino acids in certain cell wall glycopeptides. These proteins are Zn-dependent peptidases with highly conserved residues involved in cation co-ordination. MurNAc-LAA in this family is one of several peptidoglycan hydrolases (PGHs) found in bacterial and bacteriophage or prophage genomes that are involved in the degradation of the peptidoglycan. In Escherichia coli, there are five MurNAc-LAAs present: AmiA, AmiB, AmiC and AmiD that are periplasmic, and AmpD that is cytoplasmic. Three of these (AmiA, AmiB and AmiC) belong to this family, the other two (AmiD and AmpD) do not. E. coli AmiA, AmiB and AmiC play an important role in cleaving the septum to release daughter cells after cell division. In general, bacterial MurNAc-LAAs are members of the bacterial autolytic system and carry a signal peptide in their N-termini that allows their transport across the cytoplasmic membrane. However, the bacteriophage MurNAc-LAAs are endolysins since these phage-encoded enzymes break down bacterial peptidoglycan at the terminal stage of the phage reproduction cycle. As opposed to autolysins, almost all endolysins have no signal peptides and their translocation through the cytoplasmic membrane is thought to proceed with the help of phage-encoded holin proteins. The amidase catalytic module is fused to another functional module (cell wall binding module or CWBM) either at the N- or C-terminus, which is responsible for high affinity binding of the protein to the cell wall.	4.66625e-60
NZ_LN831776.1|WP_020432804.1|5143444_5144356_+|LysR-family-transcriptional-regulator	gnl|CDD|176102	cd05466, PBP2_LTTR_substrate, The substrate binding domain of LysR-type transcriptional regulators (LTTRs), a member of the type 2 periplasmic binding fold protein superfamily. This model and hierarchy represent the the substrate-binding domain of the LysR-type transcriptional regulators that form the largest family of prokaryotic transcription factor. Homologs of some of LTTRs with similar domain organizations are also found in the archaea and eukaryotic organisms. The LTTRs are composed of two functional domains joined by a linker helix involved in oligomerization: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal substrate-binding domain, which is structurally homologous to the type 2 periplasmic binding proteins. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcriptional repressor undergoes a conformational change upon substrate binding which in turn changes the DNA binding affinity of the repressor. The genes controlled by the LTTRs have diverse functional roles including amino acid biosynthesis, CO2 fixation, antibiotic resistance, degradation of aromatic compounds, oxidative stress responses, nodule formation of nitrogen-fixing bacteria, synthesis of virulence factors, toxin production, attachment and secretion, to name a few. The structural topology of this substrate-binding domain is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the substrate-binding domains from ionotropic glutamate receptors, LysR-like transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	6.2195e-57
NZ_LN831776.1|WP_020431261.1|5123076_5123541_-|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	1.56308e-22
NZ_LN831776.1|WP_020432798.1|5137217_5138657_-|AMIN-domain-containing-protein	gnl|CDD|119407	cd02696, MurNAc-LAA, N-acetylmuramoyl-L-alanine amidase or MurNAc-LAA (also known as peptidoglycan aminohydrolase, NAMLA amidase, NAMLAA, Amidase 3, and peptidoglycan amidase; EC 3.5.1.28) is an autolysin that hydrolyzes the amide bond between N-acetylmuramoyl and L-amino acids in certain cell wall glycopeptides. These proteins are Zn-dependent peptidases with highly conserved residues involved in cation co-ordination. MurNAc-LAA in this family is one of several peptidoglycan hydrolases (PGHs) found in bacterial and bacteriophage or prophage genomes that are involved in the degradation of the peptidoglycan. In Escherichia coli, there are five MurNAc-LAAs present: AmiA, AmiB, AmiC and AmiD that are periplasmic, and AmpD that is cytoplasmic. Three of these (AmiA, AmiB and AmiC) belong to this family, the other two (AmiD and AmpD) do not. E. coli AmiA, AmiB and AmiC play an important role in cleaving the septum to release daughter cells after cell division. In general, bacterial MurNAc-LAAs are members of the bacterial autolytic system and carry a signal peptide in their N-termini that allows their transport across the cytoplasmic membrane. However, the bacteriophage MurNAc-LAAs are endolysins since these phage-encoded enzymes break down bacterial peptidoglycan at the terminal stage of the phage reproduction cycle. As opposed to autolysins, almost all endolysins have no signal peptides and their translocation through the cytoplasmic membrane is thought to proceed with the help of phage-encoded holin proteins. The amidase catalytic module is fused to another functional module (cell wall binding module or CWBM) either at the N- or C-terminus, which is responsible for high affinity binding of the protein to the cell wall.	2.34153e-75
NZ_LN831776.1|WP_046504665.1|5133386_5136140_-|hypothetical-protein	gnl|CDD|306825	pfam00395, SLH, S-layer homology domain.	8.24994e-05
NZ_LN831776.1|WP_020428419.1|5128911_5129337_+|SRPBCC-domain-containing-protein	gnl|CDD|176856	cd07814, SRPBCC_CalC_Aha1-like, Putative hydrophobic ligand-binding SRPBCC domain of Micromonospora echinospora CalC, human Aha1, and related proteins. This family includes the SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain of Micromonospora echinospora CalC, human Aha1, and related proteins. Proteins in this group belong to the SRPBCC domain superfamily of proteins, which bind hydrophobic ligands. SRPBCC domains have a deep hydrophobic ligand-binding pocket. MeCalC confers resistance to the enediyne, calicheamicin gamma 1 (CLM), by a self sacrificing mechanism which results in inactivation of both CalC and the highly reactive diradical enediyne species. MeCalC can also inactivate two other enediynes, shishijimicin and namenamicin. A crucial Gly of the MeCalC CLM resistance mechanism is not conserved in this subgroup. This family also includes the C-terminal, Bet v1-like domain of Aha1, one of several co-chaperones, which regulate the dimeric chaperone Hsp90. Aha1 promotes dimerization of the N-terminal domains of Hsp90, and stimulates its low intrinsic ATPase activity, and may regulate the dwell time of Hsp90 with client proteins. Aha1 can act as either a positive or negative regulator of chaperone-dependent activation, depending on the client protein, but the mechanisms by which these opposing functions are achieved are unclear. Aha1 is upregulated in a number of tumor lines co-incident with the activation of several signaling kinases.	6.76801e-21
NZ_LN831776.1|WP_046504674.1|5140568_5141171_-|3-isopropylmalate-dehydratase-small-subunit	gnl|CDD|179314	PRK01641, leuD, 3-isopropylmalate dehydratase small subunit.	2.17757e-129
NZ_LN831776.1|WP_046504668.1|5136443_5137109_-|GerMN-domain-containing-protein	gnl|CDD|378464	pfam10646, Germane, Sporulation and spore germination. The GerMN domain is a region of approximately 100 residues that is found, duplicated, in the Bacillus GerM protein and is implicated in both sporulation and spore germination. The domain is found in a number of different bacterial species both alone and in association with other domains such as Amidase_3 pfam01520, Gmad1 and Gmad2. It is predicted to have a novel alpha-beta fold.	4.73764e-09
NZ_LN831776.1|WP_046504658.1|5117954_5118974_-|substrate-binding-domain-containing-protein	gnl|CDD|380661	cd20006, PBP1_ABC_sugar_binding-like, monosaccharide ABC transporter substrate-binding protein such as CUT2. Periplasmic sugar-binding domain of uncharacterized ABC-type transport systems that share homology with a family of pentose/hexose sugar-binding proteins of the type 1 periplasmic binding protein superfamily, which consists of two domains connected by a three-stranded hinge. The substrate specificity of this group is not known, but it is predicted to be involved in the transport of sugar-containing molecules and chemotaxis.	3.726e-105
NZ_LN831776.1|WP_020428420.1|5129340_5129673_+|winged-helix-turn-helix-transcriptional-regulator	gnl|CDD|238042	cd00090, HTH_ARSR, Arsenical Resistance Operon Repressor and similar prokaryotic, metal regulated homodimeric repressors. ARSR subfamily of helix-turn-helix bacterial transcription regulatory proteins (winged helix topology). Includes several proteins that appear to dissociate from DNA in the presence of metal ions.	2.23228e-15
NZ_LN831776.1|WP_144412128.1|5124868_5128537_-|dynamin	gnl|CDD|206739	cd09912, DLP_2, Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins. The dynamin family of large mechanochemical GTPases includes the classical dynamins and dynamin-like proteins (DLPs) that are found throughout the Eukarya. This family also includes bacterial DLPs. These proteins catalyze membrane fission during clathrin-mediated endocytosis. Dynamin consists of five domains; an N-terminal G domain that binds and hydrolyzes GTP, a middle domain (MD) involved in self-assembly and oligomerization, a pleckstrin homology (PH) domain responsible for interactions with the plasma membrane, GED, which is also involved in self-assembly, and a proline arginine rich domain (PRD) that interacts with SH3 domains on accessory proteins. To date, three vertebrate dynamin genes have been identified; dynamin 1, which is brain specific, mediates uptake of synaptic vesicles in presynaptic terminals; dynamin-2 is expressed ubiquitously and similarly participates in membrane fission; mutations in the MD, PH and GED domains of dynamin 2 have been linked to human diseases such as Charcot-Marie-Tooth peripheral neuropathy and rare forms of centronuclear myopathy. Dynamin 3 participates in megakaryocyte progenitor amplification, and is also involved in cytoplasmic enlargement and the formation of the demarcation membrane system. This family also includes mitofusins (MFN1 and MFN2 in mammals) that are involved in mitochondrial fusion. Dynamin oligomerizes into helical structures around the neck of budding vesicles in a GTP hydrolysis-dependent manner.	1.09387e-44

Protein sequences

>NZ_LN831776.1|WP_020428420.1|5129340_5129673_+|winged-helix-turn-helix-transcriptional-regulator
MSAPALKHDVFQAIADPTRRTVLQLLARNDMPIVAISENFALSRTAINKHLHILSDAGLVSSRRVGRETRYRLQPERLIELKDWLAFFETYWDDRLSLLKEFVESAPDPQ
>NZ_LN831776.1|WP_020428419.1|5128911_5129337_+|SRPBCC-domain-containing-protein
MHTEETLPEIRKTIVLNAPIDKVWKAVATSGGLAAWWMDNTFEPVLGQEFILRSGQFGDSPCKVTELEPPYRLGFDWGKDWHLAFELKELENQQTEFTLIHSGWDEAKVTEFGQPHSVIRGIMNGGWEKIVNQSLVSYIEA
>NZ_LN831776.1|WP_144412128.1|5124868_5128537_-|dynamin
MGTGRAEMLNEILKEQSYLGLRKLLEQWEDSAAVQIITDLETKAAAGELTFAFCGHFSAGKSSMINQLCGKQVLPSGPVPTSANIVSIRSGSPRVLLYPHAPETGVQPSPWETTPEQLQDFCRKGGEYAAISVWEDVPLLGSHGVLMDTPGVDSTDNGHQAATHSALHLADVVFYVMDYNHVQSENNLAFAKALSEWGKPLYLIINQIDKHREQEITIELYRRQLESAFGQWGIHPAGILFTSLKVQEHPLNQWEHLLSLIGSLLKQREELLQYSLSRSLYHTADAALGAYREEQREERERLLEEAGGDGPDSVEQELQKCAEERVRLDGLGEEARLNLRTGVDALLGNSSLMPAEVREAAGAYAESVSPGFRKGLLFTAAKREKEQQKRLAAWHTLQTREIAAQLEWHLLQLVRQWGEGLGVWDEATETQLKQAVSPEGLAAAVKPGTGFSGEALLNFCRTLAADIKAQFRRAALGAGDELLAKLPPLLDGQRAELARREAALQRQARALAALAALDRAADARAAELAAQLPPRRTLTPGTLPEVRVTPQAGALRAAPRKPQPLPQAAAGSPAAGLAAGTASPAGGRRRLGEAAAVLDAAAELLRREPAMASAARSLAARAADLAGGRFTLALFGAFSAGKSSFANALLGEEVLPVSPHPATAAVNRILAPEGDFRHASAVVTMKSREDFWEDILHSFSVLQLAAPQPETWTAAAAELQVGGLHPSALPHAGFLRAAAAGWQEAEALLGTVRTVDLQEYRTLVAEETRACFIQGIDLYYDCPLTASGIVLVDTPGADSLHARHTGVTFGYMKNADAICFVTYYNHAFSKADRGLLAQLGRIKDSFALDKMFFIINASDLASDEDELQEVQQHVAQNLRAGGLMKPQMYSLSSLLALEGKTAGSRELYEASRFSSFEQALADFAGGELPRLSLAAAKDSLSTVRRRTEEWQEKARQAAGQREAQMRELEDQCRIAEQRLRQLAGEERPGRDLRREGEELLYHVRQRISFAFGRFFQESFHPSLLREDGGNLKEIFTACGRELERTVQRELEQELWATTLRLEAAGRRLAHAAAAAAAEELSIPAEDLQFLQNDKDPWPSPARLECRLNPLDWPALWSRFKSPRHFFEGVGRNEVRAAAEPWMKESVAGAAEELESFLLDFYARSVDAALSRAGDALRESLTEREAAITELLKGGDSAEHWHRLSGELLRLEEAFDNIVDNDL
>NZ_LN831776.1|WP_046504662.1|5123530_5124721_-|formate-dependent-phosphoribosylglycinamide-formyltransferase
MWGAPFSTQSRKLLLLGSGELGKEVIIEAQRLGVETVAVDRYEAAPAMGVAHRSHVIDMLDAEALKKLIRAEKPDLIVPEIEAIATHALQELEEEGFLVVPTARAARLTMDREGIRRLAAEELGLPTAGYRFADSLDELRQAVEILGTPCVIKPIMSSSGKGQSICRKLEDAESCWNTALEGARAKGTRVIVEAFVTFESEITLLTVRSVSGTIFCPPIGHIQKDGDYVESWQPHHMSAAQLAEAEGIARAVTDQLGGFGIFGVELFLTDHGVLFSEVSPRPHDTGMVTMITQDLSEFALHVRAILGFPLDPVHLLSPGASATLKAETAGQAFRVTGIGEALALPRTQVRVFGKPEIRPGRRMAVALSAAEDVEIARTAAKQAASMLKVEVIEDEQ
>NZ_LN831776.1|WP_020431261.1|5123076_5123541_-|GNAT-family-N-acetyltransferase
MNSSTQEQVLQIRKCGLNDLERVTALLREFGYPTTLSVMKERMEDMETDPFHCTLVAELDNEVVGMVGLRKVRSYYKQADCITEITALIVAEELRGNGLGKRLVAAAEEWARQKGCCELFLRSGNRVERAPAHAFYRHIGFEKTAGYRFNKSLL
>NZ_LN831776.1|WP_020431263.1|5120797_5122447_-|response-regulator
MYKLILAEDEEDVREGIIAQIDWEQYGFEVVDQAENGREAADSIDRLLPDVVVTDIQMPFMNGLQLAEWIRNRHPNTKIIILTGYDEFEYAQKAIKLQIDEYILKPFSAQELIDVLLKVRSAIEAEIAEKENVFVLSEHYRKSLPVLREQFLSSLVSRRLRPAEIAEKSAEYGIHLRGELFQASVISVDYIREGGGGEAVSSRPVSLRDTGDRNLQLFAVLNIAEEICQKHSFGKVFIHRDNVVLLSVSEEKEEASITGRTYAILEEIRQNVQRFLKLTVTAGSGTACHSPSLLSQSFNDALQALDYRLILGNNRVIWIEDVESRVGRMLAYDELTQQSLIRTIKLGTLQELKEVVDELFGGLDAAQVSTQEYQIFLLEIITTILRVAKESGSELNDYPGLGFTSLSEIHKFNNMGEAKEWIIGVCSRLMDSIAMERQSSYKQLIDQAKDYIRSHYEESDISIGRVCQHLHISTGYFSSIFKKEMKMTFVSYLLQIRLEAAKELLRSTELKAFEIAERIGFADPNYFSFCFRKKYGQSPKEYKNSSRGG
>NZ_LN831776.1|WP_020431264.1|5118970_5120794_-|histidine-kinase
MNKPKAYFPPHRPHPRRKGKLRLPSKLRSIQLIITLTFTAVTVLVAVIVSFMLYNKFAATAEANANMNMQQIIEQVNYNLDLYAKGMANIFATAEEHITASPSIDSPLLSERMDTLMSSREDLVSIAVFTPQGKYVVGTPGQNMRINTQLQSQSWFTSAVKNPEISYSAPHIQNLFKGRYTWVVSISKMIEYKENGQIRKGILLIDFNFRTIDELSRQVKLGKRGYAYILDPLGNIVYHPQQQLIYAGLKYENVEPVLEYKFRSYLDESTGEKRFITVRTLDLTGWKIVGVAYYDEIVTTKRDLNHFLAWFLGVVIVGVIVLSILLSWLIASPIRKLERTVKLVGEGDLNTPINVSGAYEVEQLSRRFNMMLQRIRQLMDQIIYEQETKRKGELEVLQSQINPHFLYNTLNSVIRLAERGKTDEVVTMIQSLSKFFRISLSKGKNMITMQEELDHIRHYLVIQSFRFKNKFRYEISAEEEVLACQTIKLILQPIVENALYHGIEMLPDEGLITITAELVEGLIIIRVSDNGLGMSKETLGTLLSGGKSSSGSGVGVRNVNERIGLVYGREYGLAFESELEEGTTVTICFPAVQAGTEPEEGREDSVQ
>NZ_LN831776.1|WP_046504658.1|5117954_5118974_-|substrate-binding-domain-containing-protein
MKSWRLGLVLLLCTGLGLALTSCLGTSPAYISTNKTHNVHMIVKMNRGDYWNTVKLGAEAAAKEFNVKLTFKAPDSESDIDEQITMVEESIKQKADVIILAASSYMGLAQVVDRAEYYRIPVVSVDAEVGSAKVKTYVGSNGYEAGQKSAERLIDLLNGYGEIGIINFTNATSGQTSSTGTIDFGARDADEREKGFLNYAARFPNVEVVQISYTSSNTADAEQLTRDMLRNHPRLRGIATLNETASQGAGKVIQELGPGPLKMVAFDSSPSMLEMLQDGTVQATVIQNPFNNGYLAVKYAVEATEGIDVPERVDTGTKLIDLDNMLWPENQKLLFPFVR
>NZ_LN831776.1|WP_020431266.1|5116534_5117614_-|galactose/glucose-ABC-transporter-substrate-binding-protein-MglB
MKKITSVLLASALLGAALAGCGGNNNADTGNKGNTAKATNSANSGAAGGETPKVGVAIYKFDDTFMTGVRNAIDTAAKGIATVDIVDSQNSQPTQNDKVDLFITKKYDGMLINPVDRTAAGVIIDKAKTADIPVVFLNREPLPEDMKKWDKVYYVGAKAEESGTMSGQLIVDYWKAHPEADKNKDGVLQYVMLKGEPGHQDAELRTTYSIQAIEDAGIKVEKLAEDTAMWDRVKGQEKMAAFLGSHGDKIEAVLANNDDMALGAIEALKAAGYFTGDKYMPVVGVDATAPAVQALQDGTMLGTVLNDANNQGKAAITLAALLAKGEAPTKENVGFDITDNQYVWISYKKITKDNVADAK
>NZ_LN831776.1|WP_020431267.1|5114899_5116411_-|sugar-ABC-transporter-ATP-binding-protein
MAKSQFLLEMNNITKEFPGVKALDGVSLKVRPGSVHALMGENGAGKSTLMKCLFGIYSPDAGEIYLDGEKASITNSNDALGHGISMIHQELHPVPFRNVMENIWLGRFPTKGFGPLQFIDHKKMFTDTENLFKDLDIDLHPETLVGKLSVSKIQSIEIAKAVSFHSRVIVMDEPTSSLTSVEVEHLFRIIRDLQKRGVAIIYISHKMEEILEISDEVTIMRDGKKIGTWPSAELTTDLIISRMVGRDLTNRFPERQNVPGEVFLKVEGLTSTEPRSFKDVSFELRRGEILGVGGLVGAQRTEVIEALFGLRSIKSGSISIGGKKVNIQSPQDAKRHGLALLTEERRVTGIFPVLSVHENGAIANLDHYKTPYFLLDGKKKKAEVDKMIEKLRTKTPTTKTQIMNLSGGNQQKVLLARWLLTEPEVLLLDEPTRGIDVGAKFEIYSIIADLAKQGKSIIMISSEMPELLGMSDRVMVMSEGRLTGILEGDQATETEVMRLAAQH
>NZ_LN831776.1|WP_020432793.1|5132264_5132531_-|hypothetical-protein
MKCISVYTDNFEAFSDIFERVVESPLEENEEQEVEGITISHSGDVPEHYLERMSQKPEVVVMRDKSRGLTILQHGKVFEILLPVLETA
>NZ_LN831776.1|WP_020432794.1|5132575_5133247_-|endonuclease-III
MKAAEVRHILDTIGDLFPDAHCELNHSNAFELTIAVLLSAQCTDATVNKVTEDLFQKYKTPLDYISVPIEELESDIRRIGLYRNKAKHIQSLCSILIEQYGGEVPQAHDLLVTLPGVGRKTANVVVSNAFGVPAIAVDTHVERVAKRLALAGWKDSVLEVEKKLMKAVPRDEWTLTHHRLIFFGRYHCKAQNPKCQVCPLLDVCREGKKRMKTAVIRKAKSHT
>NZ_LN831776.1|WP_046504665.1|5133386_5136140_-|hypothetical-protein
MSGQKRSKRSIHTYSSKAAAAILAGTMVLGGAGAAFAAPAAPAATSGANNGSAPTAAAGIFTDVKNGFWAEKHIYKLASQGIVVGNNGLFRPGDSVTQQEAVLMALRFMKLQGNVQSDSDVVFPTDFKVTNYYKPYVVLAFQQGLLDKAAEMAPDNLKTSWGERKASREWVAELLIRALGKTTEAAAVSGKPTGFADDAKVAANKRGYINAAVGLGLANGLDGNRFDPQGAVTRAQLATFFSRAEAHNTLDYDNTVKGTISAMQDGKLTLFNNGSTSVFNVTYSTAYFTSTVDTRINFSDLKPYTKVTVIGATYNAAYVEVTDPVQQVQTIEGVFAKVTPGTIWLDSPTGYDQYSYDGSTAFVDVNGAAISASSITAASKIALLRETFSGTGKIVKVQVTSGIVNKTANGTIQSVDNAAKSITFKTAEGATETFKWEDGTTLFSSQNAVLLPADLKAGAAVKYTVKDNLIRTVEVTSGVERTVQGAITELTNSTIVYKKADGTREVNLLGTSPAVIIPGVASPGIGDLVADATAGDNVQLTLNSSDQVTKIEVLSRQISQFTGATVVDYSAKTQLLTVTDSSGKAQLVKIDANTKLAYDGATTTSLANMGYRLAEGRKVDVVAAGQRALSVETSTKYDGTLTAVNVANRTITLKLANAQQVTLPYPQSVEIFGRTSSVITDVALDSAVTAVLADNQSGVSVLRVNSSMQLEIATLDATANKLGVKWTGGTTVLNTYTLPMTDESGKSIKIGDLKVGDFVNITFNGSSPLSLQAVKLNSGQLTAVDAAAGTFTLKDYKGGAQTFSAAGGVKIIRDGSTTTSLGSLTTADRVEVRKDSDGSTIIRVLSQQNRVFWRYESGTNEILVKRASASDSNYRFVPGPNVYIHQGDTTLPVQSLKDNDNIIMYFNNNILVEIAKQ
>NZ_LN831776.1|WP_046504668.1|5136443_5137109_-|GerMN-domain-containing-protein
MNKKLTYAGIAALLLLVISGCGDKPTAAPANEQGQDSTTVVNGAGSNEGGEEATATATATVSPSASAQPTAEPTASPAATEQPTAPAKKSQSISVYYTDPQQMELVSAKTDISYADAVEKYSEAYKSLQSSSNPDQVPLWGKIELKSLKFTDGQIIMDIHKPDEAQLGAGGEAFAISALAQTLFQFEEVKSVEVLVDGEQVESLMGHVDLEHPLTRENSGL
>NZ_LN831776.1|WP_020432798.1|5137217_5138657_-|AMIN-domain-containing-protein
MKKFAFMLLLLLFVVVLPGQGHAAGGSNKIFLDGKELTAGLDVPVENVNNSIMVPLRMIAENLGYQVNWDQKSKTVTIEQQGKTIKLIVDQTAASVDDKTVVLTTAPLLRSDTTLVPIRFIGEQFGLKVTWDNTTKVVNLITPEIPDSTSNTGESSGDGGTSVAVPPVDTTANLTMVNGISFSENRLTIAMDGNSQPVVSKVTGPDRIVIDLPNATFSDVFGTGQVLSPDLNGSLAVTDYPDVSGVRYSLYSTNPYTVRFVIDLNNAKNYSVNVSGDVSKLVVVDLNAASTDDPATLPGNNGRKLVVLDAGHGAKDSGAVGVTGKYEKNFNLAVVLKAAALLKQENKVDVVLTRSDDTFLELKERAGMANNLKADLFISVHANSGSSSAASGSETYYQRAESKALANVMHKYLVQATGLSDRGVRYGNFHVIRETTMPAVLLEVGYLSNKGDEALLFSEDLQNKVAAGMVAGIKEYLKL
>NZ_LN831776.1|WP_046504672.1|5138819_5140391_-|AMIN-domain-containing-protein
MRRAGQRVLFLLLLPLLLLSFAGHEAAAAGNSAGRIVMDNRELEIPKGITLENVNGSVMIPIRVVVENLGFEVLWEQKSRKVTVQQDGKSVQLAVGSKTADADGVTLALNAAPKQTGGTVLVPIRFVSEQFGLKVGWDNSDKTVYLSGGAAGSTAAPSSPQPSAAPDPTAVPGPTSVPADSQGTDGDIVTGVTEPTPTPIPGSAGTAAGSPQVMGAVFSENRLIISVAGAAKPNVTQMGSPDRIVIDFPGAVFAPDFAGSFPGVSTSGSPQGKLDVSGYPLVTEVRYALFSVSPPTARFVIQTVGSQPYQVSKDDSTGLVTVDLNAVSSGTPPTGGTGLSGKPVVVLDAGHGGTQSGAVSLTGKLEKNFNLAVIQKAGALLMQAGLVDVIFTRTEDVTRGLQERVDIAERAKANLFISVHGNSLPADYPNRNKVNGSETYYSRAESLPLAQIMHKHLVAATGFKDNGIRSKSLHVTRESSMPAVLLEVGYLTNPGNESAMYSEQLQDSLAREIVAGIMEYLGL
>NZ_LN831776.1|WP_046504674.1|5140568_5141171_-|3-isopropylmalate-dehydratase-small-subunit
MEAFKKLTGIVAPVDRVNVDTDAIIPKQFLKRIERTGFGQFLFYEWRFDEAGNDNAAFEMNKPRYKGASILISRANFGCGSSREHAPWAIMDYGFRVVIAPSYADIFYNNCFKNGILPIKLSESQVDELFKRTAEHDGYKLTVDLENNLLSDDHGLSITFELDEHRRQFLLQGLDDIGLTLQHADEIAAYEERHAAKLFA
>NZ_LN831776.1|WP_020432802.1|5141198_5142623_-|3-isopropylmalate-dehydratase-large-subunit
MGNKTMFEKIWDNHVIHQEEGKPSIIYIDLHLVHEVTSPQAFEGLRLSGRKVRRPGLTFATMDHNVPTKDRYNITDPISKQQIDTLSQNCRDFGVKLFDLNDIDQGVVHVMGPEIGLTHPGKTIVCGDSHTSTHGAFGALAFGIGTSEVEHVLATQCLQQSKAKTMEVRFTGKRNPGVTAKDMILGVIAKYGTDFATGYVIEYTGEAIRELSMEERMTVCNMSIEGGARAGLIAPDETTFNYLRGRQYVPQGAAYEAAVETWKELVSDEGAQYDTVVEFDVETLIPQVTWGTSPGMGTNITSTVPNPADFTTENERKAAEKALEYMDLVPGTPISEIGIDYVFIGSCTNGRIEDLRAAAEVAKGHKVSDKVTAIVVPGSGRVKMQAEKEGLDKVFTEAGFEWREAGCSMCLAMNPDVLQPGQRCASTSNRNFEGRQGRGGRTHLVSPAMAAAAAIKGHFTDVRDWNYKAEAVNA
>NZ_LN831776.1|WP_020432803.1|5142858_5143317_+|hypothetical-protein
MGIQFLDMRISQDSAADQPGVSLSSSSFPYIFGDIGLQTGGIAPGNASLVRVTLNAYARLTMAISSNPAIVPDVTFTIFRNSAQIFTTVYQKPASQAMTELTYEMAGITAVDFPPAADVLAGQIRYIISVTTNYGVTLGARSFSGIAVAGNG
>NZ_LN831776.1|WP_020432804.1|5143444_5144356_+|LysR-family-transcriptional-regulator
MELRQLQYVLQIAAERNFSRAADKLHIAQPSLSQQLSKLEKELGVLLFQRNTSSVELTHAGEKFVEQAQTIIDAVELLRQEMSDISQLRTGRVVVGSMPITGAHLLPHVLPVFKSKYAEVEITLLEDSSMNLEKLTASGQTDLSLLSLPLEIPTLAYEVLGEERIDLAVPPEHPLASRSASEIRTALEELRDEPFIVLKEGQGFRKMTVELCRAAGFEPRIVFESNNMETVQSLVATGMGVTLVPHFIARAPRSEFVPVYLPLADPVPSRTLVVAYRRGRYLSHAAEAFMETFRTTVKGLSVE

Crispr_ID: NZ_LN831776_53

• CRISPR_ID: NZ_LN831776_53
• CRISPR_location: 5294130-5294204
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_53

Consensus_repeat	Method
AAGTGGAAAAAGGGACACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_53

>53.1|5294153|29|NZ_LN831776|CRISPRCasFinder
TGCCGGAGGACCCTATCCTCGGGCAGATG

CRISPR arrays and Neighbor proteins around NZ_LN831776_53

CRISPR arrays

The CRISPR arrays of NZ_LN831776_53

>merge|NZ_LN831776|53|5294130-5294204|CRISPRCasFinder
AAGTGGAAAAAGGGACACTAATTTGCCGGAGGACCCTATCCTCGGGCAGATGAAGTGGAAAAAGGGACACTAATT

>NZ_LN831776|53|54|5294130-5294204|CRISPRCasFinder
AAGTGGAAAAAGGGACACTAATT	TGCCGGAGGACCCTATCCTCGGGCAGATG
AAGTGGAAAAAGGGACACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020432378.1|5296838_5297825_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|226967
NZ_LN831776.1|WP_020426012.1|5287757_5288960_-|Ger(x)C-family-spore-germination-protein	unknown	unknown	gnl|CDD|274338
NZ_LN831776.1|WP_020432376.1|5298836_5300258_-|M20/M25/M40-family-metallo-hydrolase	unknown	unknown	gnl|CDD|349930
NZ_LN831776.1|WP_020426014.1|5286391_5286622_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426017.1|5283339_5284494_-|AI-2E-family-transporter	unknown	unknown	gnl|CDD|223701
NZ_LN831776.1|WP_020426015.1|5285621_5285981_-|(2Fe-2S)-ferredoxin-domain-containing-protein	unknown	unknown	gnl|CDD|239278
NZ_LN831776.1|WP_046504777.1|5302865_5303822_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|223674
NZ_LN831776.1|WP_020432381.1|5294883_5295129_-|transposase	unknown	unknown	gnl|CDD|222853
NZ_LN831776.1|WP_020432379.1|5296063_5296774_-|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225099
NZ_LN831776.1|WP_020426013.1|5286618_5287722_-|GerAB/ArcD/ProY-family-transporter	unknown	unknown	gnl|CDD|281794
NZ_LN831776.1|WP_020432373.1|5301983_5302853_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|224094
NZ_LN831776.1|WP_082118135.1|5295512_5295833_-|IS3-family-transposase	unknown	unknown	gnl|CDD|222853
NZ_LN831776.1|WP_020426016.1|5284651_5285461_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|225928
NZ_LN831776.1|WP_052741508.1|5300302_5301967_-|hypothetical-protein	unknown	unknown	gnl|CDD|173879
NZ_LN831776.1|WP_020426010.1|5290646_5291687_-|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|223566
NZ_LN831776.1|WP_020426009.1|5291793_5292687_-|iron-ABC-transporter-permease	unknown	unknown	gnl|CDD|376439
NZ_LN831776.1|WP_020426011.1|5288956_5290516_-|spore-germination-protein	unknown	unknown	gnl|CDD|377020
NZ_LN831776.1|WP_099091768.1|5295158_5295509_-|DDE-type-integrase/transposase/recombinase	unknown	unknown	gnl|CDD|222853
NZ_LN831776.1|WP_020426018.1|5281802_5283320_-|carboxylesterase/lipase-family-protein	unknown	unknown	gnl|CDD|225181
NZ_LN831776.1|WP_020432377.1|5297830_5298811_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|223521

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020432378.1|5296838_5297825_-|ABC-transporter-ATP-binding-protein	gnl|CDD|226967	COG4608, AppF, ABC-type oligopeptide transport system, ATPase component [Amino acid transport and metabolism].	7.05159e-149
NZ_LN831776.1|WP_020426012.1|5287757_5288960_-|Ger(x)C-family-spore-germination-protein	gnl|CDD|274338	TIGR02887, Spore_germination_protein_B3, germination protein, Ger(x)C family. Members of this protein family are restricted to endospore-forming members of the Firmicutes lineage of bacteria, including the genera Bacillus, Clostridium, Thermoanaerobacter, Carboxydothermus, etc. Members are nearly all predicted lipoproteins and belong to probable transport operons, some of which have been characterized as crucial to germination in response to alanine. Members typically have been gene symbols gerKC, gerAC, gerYC, etc. [Transport and binding proteins, Amino acids, peptides and amines, Cellular processes, Sporulation and germination].	1.13226e-88
NZ_LN831776.1|WP_020432376.1|5298836_5300258_-|M20/M25/M40-family-metallo-hydrolase	gnl|CDD|349930	cd05681, M20_dipept_Sso-CP2, uncharacterized M20 dipeptidase. Peptidase M20 family, unknown dipeptidase-like subfamily (inferred by homology to be dipeptidases). M20 dipeptidases include a large variety of bacterial enzymes including cytosolic nonspecific dipeptidase (CNDP), Xaa-methyl-His dipeptidase (anserinase),and canosinase. These dipeptidases have been shown to act on a wide range of dipeptides, but not larger peptides. For example, anserinase mainly catalyzes the hydrolysis of N-alpha-acetylhistidine while carnosinase degrades beta-alanyl-L-histidine. This family includes Sso-CP2 from Sulfolobus solfataricus.	1.77598e-116
NZ_LN831776.1|WP_020426018.1|5281802_5283320_-|carboxylesterase/lipase-family-protein	gnl|CDD|225181	COG2272, PnbA, Carboxylesterase type B [Lipid metabolism].	3.05681e-160
NZ_LN831776.1|WP_020426017.1|5283339_5284494_-|AI-2E-family-transporter	gnl|CDD|223701	COG0628, yhhT, Predicted permease, member of the PurR regulon [General function prediction only].	7.44595e-61
NZ_LN831776.1|WP_020426015.1|5285621_5285981_-|(2Fe-2S)-ferredoxin-domain-containing-protein	gnl|CDD|239278	cd02980, TRX_Fd_family, Thioredoxin (TRX)-like [2Fe-2S] Ferredoxin (Fd) family; composed of [2Fe-2S] Fds with a TRX fold (TRX-like Fds) and proteins containing domains similar to TRX-like Fd including formate dehydrogenases, NAD-reducing hydrogenases and the subunit E of NADH:ubiquinone oxidoreductase (NuoE). TRX-like Fds are soluble low-potential electron carriers containing a single [2Fe-2S] cluster. The exact role of TRX-like Fd is still unclear. It has been suggested that it may be involved in nitrogen fixation. Its homologous domains in large redox enzymes (such as Nuo and hydrogenases) function as electron carriers.	3.81519e-18
NZ_LN831776.1|WP_046504777.1|5302865_5303822_-|ABC-transporter-permease	gnl|CDD|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	8.8589e-126
NZ_LN831776.1|WP_020432381.1|5294883_5295129_-|transposase	gnl|CDD|222853	PHA02517, PHA02517, putative transposase OrfB; Reviewed.	3.38699e-20
NZ_LN831776.1|WP_020432379.1|5296063_5296774_-|GntR-family-transcriptional-regulator	gnl|CDD|225099	COG2188, PhnF, Transcriptional regulators [Transcription].	4.75546e-68
NZ_LN831776.1|WP_020426013.1|5286618_5287722_-|GerAB/ArcD/ProY-family-transporter	gnl|CDD|281794	pfam03845, Spore_permease, Spore germination protein.	2.02589e-44
NZ_LN831776.1|WP_020432373.1|5301983_5302853_-|ABC-transporter-permease	gnl|CDD|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	9.36846e-91
NZ_LN831776.1|WP_082118135.1|5295512_5295833_-|IS3-family-transposase	gnl|CDD|222853	PHA02517, PHA02517, putative transposase OrfB; Reviewed.	3.36791e-08
NZ_LN831776.1|WP_020426016.1|5284651_5285461_-|GNAT-family-N-acetyltransferase	gnl|CDD|225928	COG3393, COG3393, Predicted acetyltransferase [General function prediction only].	1.25844e-23
NZ_LN831776.1|WP_052741508.1|5300302_5301967_-|hypothetical-protein	gnl|CDD|173879	cd08514, PBP2_AppA_like, The substrate-binding component of the oligopeptide-binding protein, AppA, from Bacillus subtilis contains the type 2 periplasmic-binding fold. This family represents the substrate-binding domain of the oligopeptide-binding protein, AppA, from Bacillus subtilis and its closest homologs from other bacteria and archaea. Bacillus subtilis has three ABC-type peptide transport systems, a dipeptide-binding protein (DppA) and two oligopeptide-binding proteins (OppA and AppA) with overlapping specificity. The dipeptide (DppA) and oligopeptide (OppA) binding proteins differ in several ways. The DppA binds dipeptides and some tripeptides and also is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	1.23175e-115
NZ_LN831776.1|WP_020426010.1|5290646_5291687_-|NAD(P)/FAD-dependent-oxidoreductase	gnl|CDD|223566	COG0492, TrxB, Thioredoxin reductase [Posttranslational modification, protein turnover, chaperones].	6.70716e-64
NZ_LN831776.1|WP_020426009.1|5291793_5292687_-|iron-ABC-transporter-permease	gnl|CDD|376439	pfam01032, FecCD, FecCD transport family. This is a sub-family of bacterial binding protein-dependent transport systems family. This Pfam entry contains the inner components of this multicomponent transport system.	5.5546e-72
NZ_LN831776.1|WP_020426011.1|5288956_5290516_-|spore-germination-protein	gnl|CDD|377020	pfam03323, GerA, Bacillus/Clostridium GerA spore germination protein.	0
NZ_LN831776.1|WP_099091768.1|5295158_5295509_-|DDE-type-integrase/transposase/recombinase	gnl|CDD|222853	PHA02517, PHA02517, putative transposase OrfB; Reviewed.	4.11638e-21
NZ_LN831776.1|WP_020432377.1|5297830_5298811_-|ABC-transporter-ATP-binding-protein	gnl|CDD|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	0

Protein sequences

>NZ_LN831776.1|WP_020426009.1|5291793_5292687_-|iron-ABC-transporter-permease
MRRTTAISFDEVRRRRGLQVLAILSLLIAAALIISVNTGYIRLTPLELLHTLLGRGTDKQELILFDFRLPRIVISILVGAGLAVSGAVMQGVFRNDLADPGILGINAGAGLMVMLLLTGVAVAAGMSAAMIVLTLRLDPDKYQFVATWLAGSIWGTSWKFVLSLLPWILIQLPYVIYKARVMNVLNLGDQTVTGLGAAVTKEQFRLPGAAVGLAAANVAVSGGIGFVGLIGPHLARRLVGPKHQLLLPASALLGSLLVLTADTMGRRILQPSEIPTGIVVAVIGAPYFLYLLARTKS
>NZ_LN831776.1|WP_020426010.1|5290646_5291687_-|NAD(P)/FAD-dependent-oxidoreductase
MSKELELYDVTIIGGGPAGMYTAFYSGMRDLKTKLIEAKEELGGRMLIYPEKMIWDVGGVTPILCRKLIDQLAEQARTFDPTIVLGQQIIGQERQEDGTYILTSATGERHWTRTIILTIGYGILQMAKLEIEGADRYEVTNLHYTVQELEPFRGKRVLISGGGDSAVDWANELEPIAASVTIVHRREQFGGHEKNIARMKASSVQVRVPHTVSQLHSSDGEKIDQVTISHIESGESEQLEVDAVIVNHGLKSDFGPLKDWGLDMGEWWANVSSRLETNLPGVFAAGDFVDYSSKVRLIAGTFTDAVLALNSAKLYMDPDAPKVAYVSSHNERFKEKNKALGVVDGH
>NZ_LN831776.1|WP_020426011.1|5288956_5290516_-|spore-germination-protein
MAAQTKEKKQSQTADSNTSSPLSGNLKDDLQHIRQGLGNSMDLIIRHFKLINAALQVAVIYMEGLTDKELVDDFISHAMSFQTVSEEGQKLSTSQEVFNYIKEKALTPGKSQSLTNRGGLFEALLSGNTLVLVEGMPEALSGDTSGGEVRPVSEAGTQVSIRGSKASFTETISVNISLVRRRIKNPNLWVEPMKLGAVTQTNIAIMYIHGIADEDVLKKLREKLKEIRVDSILESGYIEQLIEGSGYSPFPTLYNTERPDTVAGNLLDGRIAVFVDGTPFVLIAPATFFMFFHTVEDYYQRFDISTLIRLLRFLCFFISMFGPAIFVAALNFHQEMIPTPLLINLASQREGVPFPAFVEALMMEVTFEIIREAGIRLPSPIGQTVSIIGGLVLGQAAVQAGIVSPAMVIVVSITGISSFTTPAFNMALSVRLLRFVIVFVSAFMGLYGIAILALMLVAHLCGLRSLGVPYMSPLGPFDPQAQKDTLIRSPIHFMKIRPRLEHKSNVRKKADKDRQGNQA
>NZ_LN831776.1|WP_020426012.1|5287757_5288960_-|Ger(x)C-family-spore-germination-protein
MKTKRLSVLVLFVLLSVNLAGCWNSRELNELAIVSGIGIDRVKETGKLRVTFQVVNPSSTTTTQGASTNQSPISIYTVNDRTVFGALRRASKQATRQLFFAHAQLLVIGESLAEGGMNEVYDIFERSHELRLNTTVLVSRDTDAESILRVLLPQESVPSVGLGKKAENTSRVWGETPKVSVFQTIKEITGGGGFTISGVRMLGSVEEGQKKASLEQTKAETSILISGQAVFNKGKLQNWIDGPEARGTQWILDKIVETNMNIDSGDQAKAIAVNVVFSKTKVKVEMRDGLPVFHIHINEEGNLNETQSVINLSDNHEIRKLETGMEKLTEEEVREAFQAAQRAECDYFNFGNELKRLHPAEWKKVDKDWNQIFAKGTLKLQVHAYIRATGLRVTPLKAPE
>NZ_LN831776.1|WP_020426013.1|5286618_5287722_-|GerAB/ArcD/ProY-family-transporter
MKKEVIGPSQVFAMIVLFELGTAIVVPIGLESGHAVWLSILMALPGGVLLYLIYNDLYRQFPNLIISGYTRKILGNYIGWPLSLLYIPVLMFNGSRNLREAGDLLISASYDRTPILIINSIMVIAVMYILNKGIEVFARTAEIYFWIMMVMGLVCNGVVIIAGLVDFKNLFPLHYKDWVDALTSAYPNIWIFPFGELVCFTTVLPFLKNSGISRKMGVTAIILSGFLLCFTHAIEISVLGLDIYSRAAFPIYTTITLVNVANFIQRLDALVILTLIIGVFFKMSIYCFAAAAITADLFKVKDYRRLVVPVGVIVLISSFISVENYTSHLNEGKLFLKYFLPVICAVVPILLFLVHRIRKRFGWYREP
>NZ_LN831776.1|WP_020426014.1|5286391_5286622_+|hypothetical-protein
MKILLIYAMLAILGLSMVISLDWLTGTPFSQSFNFLTKIFITTTYQELLVIITFLFLPVIQVAVETGKKKKKKHGH
>NZ_LN831776.1|WP_020426015.1|5285621_5285981_-|(2Fe-2S)-ferredoxin-domain-containing-protein
MTTWNLQGTLSHLLICGGSSCRKNAGEEVAEAIEDEIEKQGAASKIHTTVTECNGRCSDACIVIAYPEGVWYREMTPKAGKKLVRKMLKGKQLEDHILYTYDGGLQAQTGKGAKGKKKK
>NZ_LN831776.1|WP_020426016.1|5284651_5285461_-|GNAT-family-N-acetyltransferase
MFVSFETGDMVLQSEAFMQEEVRYNLIHRITEYPEAIRLTTADRKLIFTQSQGHNPWLWVSGELHEGQQTKLVQLLAEWVRTYEFPGISAQPETAKTFAEAFCGGQGKLYHTHMMLEAYQCLMVRKPAGVRGSLEQAKAEHVPVIAGFLAGFMKDAFGERLRAEDFLKIAAEDAASGNLYLWTEEHTPVSMAKITHRSARHARINDVYTPSVHRKQGYASALVAALCGRLLDEGLTPVLYADGKNPDSNKVYQSIGFQHAGQIADLKFD
>NZ_LN831776.1|WP_020426017.1|5283339_5284494_-|AI-2E-family-transporter
MERLQVWPEKFKKFFLNNRFVVTLLIVLLIGVNILVFAKIPFIFKPISVLLHTVAAPLLLSGIAYYLLNPLVDRMEKRSKIRRPYGIVILFLLIAGIITLILLTVIPMIRTQLVGLIDNFPKYSDQIQQEFIDLTGSKLFEQIQENVGTDFTDITSKVTTWGTSFLNNAVSGVGNFVGALTEIVLALVTTPFILFYLLRDGKRLPDYLMRFIPTALRPQTRMVMSEMNSQVASYIRGQIIVSCCIGALLYIGYLIIGLEYSLVLAIVAACTAVVPYLGPAIAITPALIVALVTSPFMLLKMVCVWTAVQLIEGKFISPQIMGKTLKIHPITIIFVIIFAGKMFGVLGIILAVPGYAVLKVVVTHVFQWFRFRSGLYKQIEETKE
>NZ_LN831776.1|WP_020426018.1|5281802_5283320_-|carboxylesterase/lipase-family-protein
MTATLVTTLYGKLQGAEEEGVKVWRGIPFAAPPVGKLRFRAPQPPQPWDSVREALAFSPVSHQPASTSSTRFGGLSPEYSEDCLYLNVWSPAEAGESLPVMVWIHGGTFVTGAGSQPMFDGACMARNGKVVLVTVNYRLGPFGFLHLSPFGGGLASNAGLLDQIAALEWVQGNIAAFGGNPQRVTVFGESAGSMSIAALLAMPAAAGLFAGAIMESGAAQSLPPQQAQEIAAALLAELGLAPGSGLELLDHLPAEQIMEAAARMTYKLSGEALSMFFQPVVEPATLPADPAEAVAGGAARGIPLLIGTNLHEGNLFFREERPGESFEQSLKSLELLMGIDDLAELAGGYPKSWEGQAAFLTDLFFWGSSIAFAESQSAAAPVWMYRFDWTVEGHPLLEKAVHGAEILYVFGNLHLLKQYGLTVTPEMQRLSEVMQKTWTAFAHHGNPSLADLEWPQYRTDSRATLIFDGETRVVQDPDADKRRRLFAAQANWPKVFSAGASDSRG
>NZ_LN831776.1|WP_020432381.1|5294883_5295129_-|transposase
MIRSMSRRGNCYDNACIESFHSILKRELIYRTKFQTQKEAQNQLFRYIEFFYNRKRIHSKLGYLSPDRFEELYYSNLALAN
>NZ_LN831776.1|WP_099091768.1|5295158_5295509_-|DDE-type-integrase/transposase/recombinase
MREHNLRSQAMGNFKVQTTDSNHDFSIAPNWLNQHFDVCTRPNQVWVTDITYIRTRQGTVYLASVLDLYTRKIVGWQLGNRMKVELVSAALDKAYSAQKPGKGLITIPIAEVSTPL
>NZ_LN831776.1|WP_082118135.1|5295512_5295833_-|IS3-family-transposase
MEPGTKGKGTNKGNAHLQQRPGLKFQFIEEHRSVFRIEKMCSVLGVSRSGYYKWRATPPSERKKHRERLVQRIEYHFHDNGEIYGSPKITKKLQQEGFTVGEKTVG
>NZ_LN831776.1|WP_020432379.1|5296063_5296774_-|GntR-family-transcriptional-regulator
MLDEKIATPLYEQLKEKLKNEIAEGRLKPGEKLLPEVELAQKYEVSVITVRRATNELRNEGLLEKRQGKGTFVAMAKYPKDLNQILSFTEASKLIGAVPSAKVLASELMIPGNDILEQLELPPGSQTVYISRLRLLDNNPMVIENNYFSIQYSFLLEENLNDHSLFQILKEKTGIQISKSKRTIEICRATMQEASYLQVSKNSPLLLVHGVVYGNNDKIVYVGNQIINGEKYKLHV
>NZ_LN831776.1|WP_020432378.1|5296838_5297825_-|ABC-transporter-ATP-binding-protein
MGNPSPYLLEVRELKKHYTSKSGLLSRKKPVVKAVDGISLNIRKGEILGLVGESGCGKSTLGRSILRLIEPTSGNIVFEGQDILAYGKEEKRMMRKELQIIFQDSGAALNPRMTVGEIIGAPLDIYGLAQGEAKERRINELLELVGLNKDYVNRFPHEFSGGQKQRIGIARALAVEPKLIVCDEPVSALDVSVRAQVLNLMKELKEKLGLTYLFISHDLSVVHHLCDRVAVMYLGKIVEITDRNELYGNPLHPYTKALLSAIPNPNPEISRERIVLEGDVPSPSNPPPGCSFHTRCPYRMDKCSVEVPILLQTQGNHSVSCHLYNDEH
>NZ_LN831776.1|WP_020432377.1|5297830_5298811_-|ABC-transporter-ATP-binding-protein
MSDYLLEVKGLKTYFNHFNKQVPAVNGVDFVVRKGETLGIVGESGCGKSVTAMSILKLLAPEAKIVDGQVLFKGKDLVGLNDRQMTRIRGNEISIIFQEPMTSLNPAYTVGYQIGEAIRTHQKLDKKTTRSRAVEMLKLVGIPDPDKRVDEYPHELSGGMRQRVMIAMALSCNPELLIADEPTTALDVTVQAQILELMKSLKDKFHTSIMMITHDLGVVAEMADYVIVMYAGTVVEYSDVKSLYNKPLHPYTEGLMNSLPKIDDPKDKLEAIPGSVPSLYDLPKGCSFWPRCPYAQEICKQEKPELYEVDQRKVRCFLYSGKIERR
>NZ_LN831776.1|WP_020432376.1|5298836_5300258_-|M20/M25/M40-family-metallo-hydrolase
MELTEMKDVFDYLEQHFEEDLKSTQEFMRLKSISATGEGIRETAQVVKAMIEEVGGASEIIETPGHPIVYGKLDEGAQYTLLIYSMYDVLPAEEPDWISDPWAAEIHDFQDYGKCIIGRGAVNTKGPTAAFFNTIKAYKKIKGKLPVNLVFLIEGEEELSSKSLQQFLVDNKDKFAECDAMFFPSFGEENRVASIFMGVKGIVSFELKAKGGSWGGPKERGIHGAFAAWVGNPAWRLVKALSTMVGEDEKEILVEGFYDGILPLAKEGEDALDASADLLDEEQWKKAYAIDRFKWDLEGLDLWKKMLTVPTLNIDGIKGGYIGEGSKTLLPHETTVKMDIRLVPGMDPEKMLGKIRNHLDKHGYSDIEITEYGKAYYPSSVPYYSTSVQTLKRMYELMGARPQIWPWNPGSAPYFLFGKILGLPYVTGGMGHGSRQHSSNEYCTVKGVLDFEKSMVYYLNLFPQVAEEMKNRE
>NZ_LN831776.1|WP_052741508.1|5300302_5301967_-|hypothetical-protein
MKKNNRLLFVLVMMLTASLLLFGCSSNAGNTAGNASSPPGTEASPQPQSEGGAASGIVTMAIISTWDTLNIYNTSGNYGNAVADQLFERLVFREHGGNVIPRLAKSWAMADDNLSMTFELADNVTWHDGEKLTAKDIVFTVQAMTNPAVNNYYRSAFNVLAGTDADGIAQDPAKVGVEAVSDTSVKFTFKEPKAEETILNAFLSFLYVLPEHILGQGDPASINTSGFWNAPVGAGPFKFVKQTAGESLQLEAFTDYYQGSPGFKTLVVRVVPAANLTAGLINGDIDVVAMGSIPLSDWDTVKNNPDIVASSIPDYSYQYMLFNLSKDTFQDSNVRTAFDKAINKTLIVDNLMKGEGGVAVGPMPKYHPYYNQSLVPNAYNPDEAKQMLEAAGFDFKREYLLIVPQGNQVREQSALLIQQDLAAIGVKVKIETYDFATLLSMLKNGESDLGLLGGGSNIDPGESSVIMKPGDSRNYSLLKDSKWYDIAAKGFSLYDFDQRKAVYDEYQQALVKDQPYIWLYHQNNLWAHSSRLTDVPMEDFVWMNFASWKWKIAK
>NZ_LN831776.1|WP_020432373.1|5301983_5302853_-|ABC-transporter-permease
MVKANSRKRTVFLNFMKRYCHNKLAIAGLVSIVLIGLLVAFLPPFLQYAEDQIDPLAFSAAPGGSHLLGTDDVGRDVLSRLLNGGRVSLFVGILSALISVALGIPLGLLAAFFRGKFETVTMRLADIFLSFPNIILILFLVSIFGPSIITVTVVIGVLGWPFFARLMFGTVLSIKEKDYIEGAAAIGEKQRTIIFKYILPNAIAPILIQITFRIAGAIILESSLSFLGMGVQPPAASWGNMLYNAQSITILSERPWMWLPPGLLLILTILSINFVGNGLRDALDPKTRL
>NZ_LN831776.1|WP_046504777.1|5302865_5303822_-|ABC-transporter-permease
MMKTYVLRRLLIALPTFLGITILVFFVSYLASGSPLELLLSNQNISEAEIERQRIKLGLDQPVYMQYFSWLGNMLTGNFGESYRTMEAVTSMILKGLGATSILVVASVLLACLIAIPLGIQSARHQSKLWDNLAAVFSFLATSTPSFFIALVLLYLFSVKLQLLPIGGMYTVGTANSFLSLLAHLIMPCLVLSFHMMGTLIQFTRSSMLEVMREDYVRTAKAKGLQERVLIVRHVLRNSLIPVATYLGMEIPLLLGGAVVTEQVFSWPGIGKLMIQSISARDYPVIMGVTVLVALAVLIFNLITDLVYGLLDPRIRYD

Crispr_ID: NZ_LN831776_54

• CRISPR_ID: NZ_LN831776_54
• CRISPR_location: 5343260-5343333
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_54

Consensus_repeat	Method
TAAGTGGAAAAAGTATCACTAAT	CRISPRCasFinder

spacers of NZ_LN831776_54

>54.1|5343283|28|NZ_LN831776|CRISPRCasFinder
ATGACCGAGCATCAAGTAACTCGGTAGC

CRISPR arrays and Neighbor proteins around NZ_LN831776_54

CRISPR arrays

The CRISPR arrays of NZ_LN831776_54

>merge|NZ_LN831776|54|5343260-5343333|CRISPRCasFinder
TAAGTGGAAAAAGTATCACTAATATGACCGAGCATCAAGTAACTCGGTAGCTAAGTGGAAAAAGTATCACTAAT

>NZ_LN831776|54|55|5343260-5343333|CRISPRCasFinder
TAAGTGGAAAAAGTATCACTAAT	ATGACCGAGCATCAAGTAACTCGGTAGC
TAAGTGGAAAAAGTATCACTAAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020430357.1|5335274_5337374_-|S-layer-homology-domain-containing-protein	unknown	unknown	gnl|CDD|306825
NZ_LN831776.1|WP_046504825.1|5347689_5349291_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|173877
NZ_LN831776.1|WP_020430356.1|5338309_5339065_-|RNA-polymerase-sporulation-sigma-factor-SigF	unknown	unknown	gnl|CDD|180137
NZ_LN831776.1|WP_020429668.1|5351585_5353112_-|PucR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|377939
NZ_LN831776.1|WP_020429672.1|5346262_5347546_-|ArgE/DapE-family-deacylase	unknown	unknown	gnl|CDD|349933
NZ_LN831776.1|WP_046504813.1|5327659_5328004_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_052741511.1|5342904_5343192_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_052741509.1|5324896_5326441_-|hypothetical-protein	unknown	unknown	gnl|CDD|274730
NZ_LN831776.1|WP_020430355.1|5339076_5339532_-|anti-sigma-F-factor	unknown	unknown	gnl|CDD|179626
NZ_LN831776.1|WP_020429673.1|5344885_5345863_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|223521
NZ_LN831776.1|WP_020429666.1|5354354_5355248_-|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|100107
NZ_LN831776.1|WP_020429674.1|5343926_5344889_-|dipeptide-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|236898
NZ_LN831776.1|WP_046504817.1|5341570_5342611_-|acyltransferase-family-protein	unknown	unknown	gnl|CDD|226122
NZ_LN831776.1|WP_039789412.1|5350321_5351299_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|223674
NZ_LN831776.1|WP_020429665.1|5355304_5356738_-|multidrug-efflux-MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_LN831776.1|WP_046504810.1|5324299_5324827_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_039789900.1|5340056_5341250_-|D-alanyl-D-alanine-carboxypeptidase	unknown	unknown	gnl|CDD|224600
NZ_LN831776.1|WP_020430354.1|5339528_5339882_-|anti-sigma-F-factor-antagonist	unknown	unknown	gnl|CDD|131932
NZ_LN831776.1|WP_020429670.1|5349400_5350300_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|224094
NZ_LN831776.1|WP_020429667.1|5353570_5354272_-|DsbA-family-oxidoreductase	unknown	unknown	gnl|CDD|239322

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020430357.1|5335274_5337374_-|S-layer-homology-domain-containing-protein	gnl|CDD|306825	pfam00395, SLH, S-layer homology domain.	2.51788e-10
NZ_LN831776.1|WP_046504825.1|5347689_5349291_-|ABC-transporter-substrate-binding-protein	gnl|CDD|173877	cd08512, PBP2_NikA_DppA_OppA_like_7, The substrate-binding component of an uncharacterized ABC-type nickel/dipeptide/oligopeptide-like import system contains the type 2 periplasmic binding fold. This CD represents the substrate-binding domain of an uncharacterized ATP-binding cassette (ABC) type nickel/dipeptide/oligopeptide-like transporter. The oligopeptide-binding protein OppA and the dipeptide-binding protein DppA show significant sequence similarity to NikA, the initial nickel receptor. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	8.24713e-173
NZ_LN831776.1|WP_020430356.1|5338309_5339065_-|RNA-polymerase-sporulation-sigma-factor-SigF	gnl|CDD|180137	PRK05572, PRK05572, RNA polymerase sporulation sigma factor, SigF/SigG family.	2.88876e-166
NZ_LN831776.1|WP_020429668.1|5351585_5353112_-|PucR-family-transcriptional-regulator	gnl|CDD|377939	pfam07905, PucR, Purine catabolism regulatory protein-like family. The bacterial proteins found in this family are similar to the purine catabolism regulatory protein expressed by Bacillus subtilis (PucR). PucR is thought to be a transcriptional activator involved in the induction of the purine degradation pathway, and may contain a LysR-like DNA-binding domain. It is similar to LysR-type regulators in that it represses its own expression. The other members of this family are also annotated as being putative regulatory proteins.	9.90918e-39
NZ_LN831776.1|WP_020429667.1|5353570_5354272_-|DsbA-family-oxidoreductase	gnl|CDD|239322	cd03024, DsbA_FrnE, DsbA family, FrnE subfamily; FrnE is a DsbA-like protein containing a CXXC motif. It is presumed to be a thiol oxidoreductase involved in polyketide biosynthesis, specifically in the production of the aromatic antibiotics frenolicin and nanaomycins.	4.79503e-73
NZ_LN831776.1|WP_020429674.1|5343926_5344889_-|dipeptide-ABC-transporter-ATP-binding-protein	gnl|CDD|236898	PRK11308, dppF, dipeptide transporter ATP-binding subunit; Provisional.	5.50131e-168
NZ_LN831776.1|WP_052741509.1|5324896_5326441_-|hypothetical-protein	gnl|CDD|274730	TIGR03696, tRNA_nuclease_WapA, RHS repeat-associated core domain. This model represents a conserved unique core sequence shared by large numbers of proteins. It is occasional in the Archaea Methanosarcina barkeri) but common in bacteria and eukaryotes. Most fall into two large classes. One class consists of long proteins in which two classes of repeats are abundant: an FG-GAP repeat (pfam01839) class, and an RHS repeat (pfam05593) or YD repeat (TIGR01643). This class includes secreted bacterial insecticidal toxins and intercellular signalling proteins such as the teneurins in animals. The other class consists of uncharacterized proteins shorter than 400 amino acids, where this core domain of about 75 amino acids tends to occur in the N-terminal half. Over twenty such proteins are found in Pseudomonas putida alone; little sequence similarity or repeat structure is found among these proteins outside the region modeled by this domain.	1.29846e-12
NZ_LN831776.1|WP_020430355.1|5339076_5339532_-|anti-sigma-F-factor	gnl|CDD|179626	PRK03660, PRK03660, anti-sigma F factor; Provisional.	1.04047e-82
NZ_LN831776.1|WP_020429673.1|5344885_5345863_-|ABC-transporter-ATP-binding-protein	gnl|CDD|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	0
NZ_LN831776.1|WP_020429666.1|5354354_5355248_-|class-I-SAM-dependent-methyltransferase	gnl|CDD|100107	cd02440, AdoMet_MTases, S-adenosylmethionine-dependent methyltransferases (SAM or AdoMet-MTase), class I; AdoMet-MTases are enzymes that use S-adenosyl-L-methionine (SAM or AdoMet) as a substrate for methyltransfer, creating the product S-adenosyl-L-homocysteine (AdoHcy). There are at least five structurally distinct families of AdoMet-MTases, class I being the largest and most diverse. Within this class enzymes can be classified by different substrate specificities (small molecules, lipids, nucleic acids, etc.) and different target atoms for methylation (nitrogen, oxygen, carbon, sulfur, etc.).	2.86069e-13
NZ_LN831776.1|WP_046504817.1|5341570_5342611_-|acyltransferase-family-protein	gnl|CDD|226122	COG3594, NolL, Fucose 4-O-acetylase and related acetyltransferases [Carbohydrate transport and metabolism].	2.21462e-14
NZ_LN831776.1|WP_039789412.1|5350321_5351299_-|ABC-transporter-permease	gnl|CDD|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	2.35403e-119
NZ_LN831776.1|WP_020429665.1|5355304_5356738_-|multidrug-efflux-MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	1.7204e-90
NZ_LN831776.1|WP_020429672.1|5346262_5347546_-|ArgE/DapE-family-deacylase	gnl|CDD|349933	cd08011, M20_ArgE_DapE-like, M20 Peptidases with similarity to acetylornithine deacetylases and succinyl-diaminopimelate desuccinylases. Peptidase M20 family, uncharacterized protein subfamily with similarity to acetylornithine deacetylase/succinyl-diaminopimelate desuccinylase (ArgE/DapE) subfamily. This group includes the hypothetical protein ygeY from Escherichia coli, a putative deacetylase, but many in this subfamily are classified as unassigned peptidases. ArgE/DapE enzymes catalyze analogous reactions and share a common activator, the metal ion (usually Co2+ or Zn2+). ArgE catalyzes a broad range of substrates, including N-acetylornithine, alpha-N-acetylmethionine and alpha-N-formylmethionine, while DapE catalyzes the hydrolysis of N-succinyl-L,L-diaminopimelate (L,L-SDAP) to L,L-diaminopimelate and succinate. Proteins in this subfamily are mostly archaeal, and have been inferred by homology as being related to both ArgE and DapE.	5.64533e-99
NZ_LN831776.1|WP_039789900.1|5340056_5341250_-|D-alanyl-D-alanine-carboxypeptidase	gnl|CDD|224600	COG1686, DacC, D-alanyl-D-alanine carboxypeptidase [Cell envelope biogenesis, outer membrane].	6.58639e-118
NZ_LN831776.1|WP_020430354.1|5339528_5339882_-|anti-sigma-F-factor-antagonist	gnl|CDD|131932	TIGR02886, Anti-sigma_F_factor_antagonist, anti-sigma F factor antagonist. The anti-sigma F factor antagonist, also called stage II sporulation protein AA, is a protein universal among endospore-forming bacteria, all of which belong to the Firmcutes [Regulatory functions, Protein interactions, Cellular processes, Sporulation and germination].	1.57522e-51
NZ_LN831776.1|WP_020429670.1|5349400_5350300_-|ABC-transporter-permease	gnl|CDD|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	7.70538e-108

Protein sequences

>NZ_LN831776.1|WP_052741511.1|5342904_5343192_+|hypothetical-protein
MYGADGGVYGADGGVYGADGGVCGTDGGVWGQTAGCVGQTAGCGTLGGVYGANGGVCGADGGVWGTDGGVCGKKGGSWRQCGIIKGRSTFDLSPG
>NZ_LN831776.1|WP_046504817.1|5341570_5342611_-|acyltransferase-family-protein
MNKQRELWIDAAKGFSIIFVVMGHSGDAAANHYLSWFRMPLFFILSGLVFKPVDSCRYLGWAAKRTKGLMTPYAAYGMLIATVLLLFSFNFRDFAENIARLLYGGLSLTGPYGVFWFITCLLFTQLLFGYIVRYPMRTQLLLITAAYSLSHLISLTSLHTFNLPWNIDVSLLAVTYYAVGYYGKKAIPALIRRRITLPLLLPLCAGVFALERAGMIHYSLNMKYKEYDAVVLDLFIPLLVSLTICAGVYWLSRHFQLQWLGNLGRNTIAIMYLHLPVNYALKYLVGADYGLVPFTLVGVGVPLLAALWISRFPLLSKLYLGHHGGSRPAVSYSERTAVRSSVSPGD
>NZ_LN831776.1|WP_039789900.1|5340056_5341250_-|D-alanyl-D-alanine-carboxypeptidase
MRYVLLVLCVAASVLGSASGAYAEEKAKAKDTGKNAAVVNLAPGARSAILMDANTGTVVYEKNSHDKLPPASITKIMTMLLTVEALDEGKLQLTDKVRTSEYAASMGGSQIFLEPGEEMTVDEMLKGIAMASGNDASVAMAEKLAGSESAFVDLMNQRAGELGLKDTHFANCNGLPAENHYSSAHDIAVISKELLKHERIIKYTGSYQDYLRKDTTKPFWLVNTNKLVRFYTGADGLKTGYTAEAKFCLSATAARDGLRAIAVVLGEPNTKTRNSEVSGMFDYLFSQYKVHTIHKAGEAIGNVKIEKGVKTKLPLTAKETYSVLLKKGITQEGIRHELVVPESIKAPVKAGQAVGKLVVYQGTDKIKEYELKADTDVPKAGWWKLFKRTAGSMFRVD
>NZ_LN831776.1|WP_020430354.1|5339528_5339882_-|anti-sigma-F-factor-antagonist
MNSHVEMEHHRGVLIVRLSGELDHHAAEYVRMDMDEAIMRGQVEHLILSLKELQFMDSSGLGVILGRYKLIRSKGGKMVVCDAAPPVQRLLEMSGLFKIMPLYDDESAALSDLEVAL
>NZ_LN831776.1|WP_020430355.1|5339076_5339532_-|anti-sigma-F-factor
MTKSEAGNFMNVQFAALSENESFARVVVAAFVSRLDPTMEELNDLKTVVSEAVTNCIIHGYDSDPEGIVSISASIEHETVHLTIEDKGRGIEDLELAQQPLYTSKPELERSGMGFTIMENFMDEFEVTSEPGRGTSISMKKTIVSKKALYN
>NZ_LN831776.1|WP_020430356.1|5338309_5339065_-|RNA-polymerase-sporulation-sigma-factor-SigF
MDAESKKAPPTYLDDAEVKRLIALSQAGDNLARDTLVNCNIRLVWSVVQRFMNRGYEPDDLFQIGCIGLLKSVDKFDLSYEVKFSTYAVPMIIGEIQRFLRDDGTLKVSRSLKEMANRVRKMKDEMSKTLDRLPTIGEVAEALGVTPEEIVFAQEANKPPTSIHETVFENDGDPITLIDQIADETQERWFDKLALNEAIGALTERERLIVYLRYYRDQTQSEVASRLGISQVQVSRLEKKILASIREQIAQ
>NZ_LN831776.1|WP_020430357.1|5335274_5337374_-|S-layer-homology-domain-containing-protein
MRFGRKRKFTQTVTAVCAAVILLGGLAGSGLGIGQASVSAAAVTAANPGRTDYSVSGDRLLWLEPDADGVKQVHALNQRSGANTVLTSGPSAKDAPYVHGAVAVWADKGSEPGSSLHWDIYTADLETGKKMKLNKQAGQYGNPTTDGAGVVWYERKNYGSMIYHDLATGVEADLGEGRFPVLAGGNVVYKNARDGGLSLLDVSSGVTRPLVSLGGANAVDWFVFNGSHVLYKQKNSATGSKYVLLNIKDLTAQPVDLTGMKAGGTEYAFMSIGEEQAVFQEEVDDAVTLKQVDLTTYAVKPLPIDAGVKLIGISGNKLLYSKKDDYIESVDLKENPNPTPGPETTPPPGATPNPGPDANPGPAPGTKIPVITGAKDSRIIGSSGGILSAVNGWARLEISAGTFPDNTSVSLAQAELETKELLDASGKKLLKAGSAWQVQASAPFLIPAKLAVRYPQEEPWTSKREKLGIYSYNPDKGIWSYIGGVTAAEDGFVQAKISASGLYAVMLREAQFTDISGHWAQQDVEVLAARGIVNGMNGTVFAPKAVLTRAEFTKLLTAALGLQPVHTDKPTFRDVSAAHWSYPYVEAAAAAGIVTGDAGLFHGNAPLTREQMMVMLMRAIDSTTAHSPASAADSVKLQAVLSGFKDNGTISQWARESVAAAVDKKLVQGSGQFLKPKDSSTRAEAAVIMYKLLAELKLL
>NZ_LN831776.1|WP_046504813.1|5327659_5328004_-|hypothetical-protein
MQWIILIGNEHFNLKLIRDLQHDGENTITSLNTNRFVVDYGNDHVFYESVEDIINDYEEDDIKRIPFPNPHFIMMTYTNGKLMKQILSQDNFPRGIYIDDDNGNILPIEEFIVS
>NZ_LN831776.1|WP_052741509.1|5324896_5326441_-|hypothetical-protein
MDVLLQAAALAAGPQVLESNRWDASNRLIKNTNTYGDITTYQYDGDGNRVSMRTTVGDGAVQDAYLPGNPAGNRDGWEPQFKKRQLELYFTNDITMSIPQPLMATGAAGQNWKQSYVYGAGEERISMSYLVSGDKSNDWEPAAGASGASAAAGTPKTLFYLSDAQGSVIGLEGQDGSMSARYRYDEFGVAEAPEKFDLNWSGPDNLFGYTSLGYDYYSGYSHAQARDFDSSIGRFISEDTYEGQLNDPLSLNLYAYVKNNPLRYTDPSGNKPWEPYDVNELRLLLNDAIAHKLNKGSDLYNAYYNKIWERYGFEDFMEKSQYSYYFKLLTGNSSGKNNASNANAAREELVSAFFDANLATYIASMAMEGSTHVSTVKIKSPTVTDSEAVVTKGTGKTGTVWDSMKATQPLYEGTQIPKSFEISVGNQKVWVHGNATEHMYEDVAKVMKTPGIDPKLYSQQLLTDFQGSLQQATQNGIKYGELMNVGKWEFKFSPPREQGQLPALIHAQFNGWGK
>NZ_LN831776.1|WP_046504810.1|5324299_5324827_-|hypothetical-protein
MLNVRKLANIVEELLEIDPYIPIKIRWGKWNEILDPTIYWRTGDFKKSLIEIGISSESGLIRTVTVVHSDKIISDSTGINWPDIVQEGTPIFKVSNWPENGRLDENGAFEIWLSKTEVNLVLSKNTIVKKVISGRVCFGLDSCSNVCLVSVCTLSDEEEMQVKDTLEYMIRQNQI
>NZ_LN831776.1|WP_020429674.1|5343926_5344889_-|dipeptide-ABC-transporter-ATP-binding-protein
MSAILEVRNLKKHYPIRKGFFAKQVGAVKAVDGITLSVEKGETLAVVGESGCGKSTTGRAILRLIEPTDGEILFDGTDVRSLDTEQLRRFRTDMQMVFQDPYASLDPRWTVQRILEEPLRTHGAAKSNELKSRVEELMQVVGLSPYQAHRFPHEFSGGQRQRIGIARALALNPKFIVCDEPVSALDVSIQAQVLNLMQDLQEQYGLTYMFISHDLSVVKFISDRVAVMYLGRIVELAPTKELFAKPLHPYTQALMSAVPVPNPGLKKSRIVLTGDVPNPETPPSGCAFHPRCPFAMDKCRKDEPVLRQLDSGHQVSCHLY
>NZ_LN831776.1|WP_020429673.1|5344885_5345863_-|ABC-transporter-ATP-binding-protein
MTELLEVSGLCTEFSTAAGTIRAVDGISLSVRKGETLGIVGESGCGKSITSLSIMQLLPKRISRIAAGQIRFEGKDMLKMPVKEVRGIRGNRIAMIFQEPMTSLNPVFKIGRQISESARFHLKLSKKEADERAVEMLRKVGIPRPEKIAQQYAHQLSGGMRQRVMIAMAMVCSPQLLIADEPTTALDVTIQAQILDLMRELQQTEGMSILMITHDLGVVAEMCDRVVIMYAGQIVEEADVATLFGKPLHPYTQGLLASLPQLAGENDRLTSIPGQVPNPANLPSGCRFAPRCPAAVDRCWAERPELLEIRPGHSCRCLLQQEEVS
>NZ_LN831776.1|WP_020429672.1|5346262_5347546_-|ArgE/DapE-family-deacylase
MTDWKSKVLSAIDAEQEQLLELCSQLIRFPSENPPGDSRDISSFIMEYLKQAGIDTEVHPATETMLNLVSTLKTGAAEPSDKKLIFCGHTDVVPAGDRSRWDFDPFCGDIVDGYLLGRGASDMKAGLAGLIYAMGLLSRLGVPLRGDLALLVVPDEETGGHLGVPWVLERELVTGTAAVIAEPSGPLNPTIGQKGSCWFEFTVEGTPGHGSLAPVVGESAIVKAAKGIEALQRLWDIKPDIPEEVQEIIRISQDYVKEREQDGSIAYQVFDHVTVNIGTIQGGTKVNVVADRCTVQVDSRVPFGVDYRDVLDRARSLLLEAGIESEVKGFGFQGNANWTSTEEPIVSNLVESICEVSGEEAYGVLQWASSDARHFRTHQIPVLQYGPAELSTIHNFNEKAPVWQIIQCAKVYALTALKYLGVEESGK
>NZ_LN831776.1|WP_046504825.1|5347689_5349291_-|ABC-transporter-substrate-binding-protein
MKRVKLLSTLTAFSILLAGCASSANPQTPAATTAAESTAAPAAAAKPFLTVAYSEGGTTLDPAEANDLTSDTLVLAAYDQLVTYGIKSDNGANIANTEDIKPMLAESWEVSSDNTVYTFKLKSGVKFQSGNPVDADSVVYSLDRVAKSSSGSFLYGMAAIKTVTAKDDSTVEIALTNANHNFLQILAMYTFSIVDKKTVEAQGADYLKTHAAGSGPFTLEKWDPATEAVFTPNDDYWQGAPKLGKVTMKFTKEASNRVLLLNKGDVDMAIEIPPKDVDTLKSNSNLTVASNASNRILYFAMNNKVKPFDNEKVRQAINYAIPYDELLTGVMYGQAKQMKSSVASNTPGFSDAGYVYEHNLDKAKALLKEAGYEKGFTFDFTLGSGFDDWEDDAVLIQAELAKIGVTMNINKLARAQFLEQQKTKNLTAYISKWTSFVNDPGYHLGFLMYGKGSSNYNNYQNAEVDKLWEQANTETDAAKRAELYKQAQEIITTEAPWAYLYEYNRIVGMSNKISGYAFYPDEVIRFYPLSIQE
>NZ_LN831776.1|WP_020429670.1|5349400_5350300_-|ABC-transporter-permease
MSTAAHSAQGSPSAPAAAHKPKTLIRLLLHNRLAAIGLVLIVIWTVTALIAPWIAPHDPYLTDMANKLQAPSGSHWFGTDNFGRDIFSRVLYGARISIWTGLIAVAISFLIGVPLGGVAAYYGGRTGTIIMRLMDVLLSFPSLVLSMAIAASIGAGLTSAMIAVGIVGIPEFARLMFGQTVSLREKEYVEASRAIGVKNSVILYRHILPNALAPLMVQATLGMGFAILTASSLSFLGLGVKPPIAEWGAMISEGREYIISGQWWLVTFPGLGIATSILGFNLLGDGFRDVLDPRLRSGK
>NZ_LN831776.1|WP_039789412.1|5350321_5351299_-|ABC-transporter-permease
MIPALLGIIVITFILSRVLPGDPAIMLAGEQAPEETVNKIRQDMGLDKPLYIQFFSYFGQLFQGNIGYAYHTGHSVASDLATRFPATLELTIASILIAILVAIPVGIIAATRKESVLDHISRVFSLIGACVPIFWLGLMFIYIFYSILGWAPAPMGRISGDLNPPSHITGLYVLDSILSGDMVALKSSIVHLVLPAICLSTGTMAIVARMTRSSMLEVVDQDFVRTARAKGLKESAVIYKHALVNALIPTLTVLGLQFGYLMGGAVITETIFSWPGIGGYVTDSILAADYAPIQAFTLVSAILYCGINLAVDLIYGLIDPRIRYE
>NZ_LN831776.1|WP_020429668.1|5351585_5353112_-|PucR-family-transcriptional-regulator
MNTRGITLRELMQLPILSKATVISGMQGLDRVVRFVDVMEVPDLKGWISEGVMLLTTAYSIRHDPSLLTELIYTLDQLGAAALAIKPARFLKEIPQGAIEASNDCGLPIVEIPPEIPYTDITQPVMELLLGRQAMLLRRAEEVYRTLTTMVLENSGIQAVSDNVADFLKAPVALLDTERNIIVSSPSQFDWSLAERPLSWNIHVDRRTVARLLVDKEQLDDMEEVGIEQARLVFALELMRKKVAEDTEFRLRGNFIDELLTPPLPSRHEVERRARQLGMNPEHKWEVAVIEGETAPNEETVNRLLEQEARKRGVTPHAEFRSNRAVLFLPTPEGRKFGVAGDKGTSWAVTLEGWLSDKAEGLGGYRTGVGTPEYLWDIQTSYNEARKALSVAKRLGQGTGGVTRYEEIEVYHLLEGLSGEGFAALFERKLGKLRQYDQEHDSNMLLTFYHYLECRGSLIETANSLYIHRNSVKYRLERIRDITGFDLNDPREQFVCHLCLIYYYLQEK
>NZ_LN831776.1|WP_020429667.1|5353570_5354272_-|DsbA-family-oxidoreductase
MRIDIWSDFGCPFCVIGKRKFENALGMFTMKDKVDVVYRSYQLDPNAENRTLSNEQLAQEKGMNVEQLKAKQAHVANMIKKEAGFDVSYDQVVIANTFDGHRLVHFADKAGKGAELTERLFRAYLSQRMNIADHNVLVALGSEAGLNEQYVAEMLKSDAYKDSVKADIAEARNLNISSLPTFVFNNKYVISGAQSEEVFLNALNSIWEKEKVLQELEKTEQSSGEDGCEVGQW
>NZ_LN831776.1|WP_020429666.1|5354354_5355248_-|class-I-SAM-dependent-methyltransferase
MNDDFFNAAMWEKVWKDESDLKIDRMKKSGIDPTRSFDHKAKVFNEQSFNEKGRQRTKRIISWLEGQGVQFENASVLDIGAASGVFSVPFAEKGARVTAVETSPPLIELLEENVANFAEGQVKIVPEPFEDIDVASMGWNQTFDLVFASMIPIIHNWESVEKILQCARKFCYISMPVLHTEHSLVKEIWPLVTGQSYQSKLTEMGYLLHLLYLKGYAYETLVTAEGKTREIPGEMALQEVMTWLGHHRLPADERNMRIVANYLEQSYPSGKVVVQEGGRYGKVLIRLQDQYMYTRKN
>NZ_LN831776.1|WP_020429665.1|5355304_5356738_-|multidrug-efflux-MFS-transporter
MIDLNNIRRGPIMLALIIGMFVAALNETLMGNALPALMQSFDASAATVQWLSTAYMLVVGVLVPITAILQQWFTTRQLFLSAMGLFFIGTVISAVSPVFSVLLIGRIIQAVGTGMLLPLVMNVIMTIYPPEKRGGAMGMLGLVVMFAPAIGPTISGLIVDGLSWRWLFYLVIPFALISIFVGAAVLKNVSEVTKPRIDFLSIVLSTIGFGGIVYGFSSAGEHGWAVPEVIWTIAVGGVALLLFVWRQLKLEQPIMDLRAFRYPTFALVAVLLFVLMMTFFSSAIMLPMFMQGVLLITAFKSGLILLPGGIVNGVMAPISGKLFDKFGPRILIIPGLTIAVISLWQFTRFNEATSTGFIVSVHIALMIGIALVMMPAQTTGLNQLPRNLHPHGTAILNTLQQVAGAIGTALYISIMSGGQKQYLSGVSDPSASSEITKGLAAGINNAFWFGVIVALIALGIGLFLRKGKSPEHEQLAE

Crispr_ID: NZ_LN831776_55

• CRISPR_ID: NZ_LN831776_55
• CRISPR_location: 5379342-5379430
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_55

Consensus_repeat	Method
CTTAAAGTTTTGTAAGCGATGCTTAC	CRISPRCasFinder

spacers of NZ_LN831776_55

>55.1|5379368|37|NZ_LN831776|CRISPRCasFinder
AGATATGACTTCGTACAAAACTCGCTTCGAAAGCTTC

CRISPR arrays and Neighbor proteins around NZ_LN831776_55

CRISPR arrays

The CRISPR arrays of NZ_LN831776_55

>merge|NZ_LN831776|55|5379342-5379430|CRISPRCasFinder
CTTAAAGTTTTGTAAGCGATGCTTACAGATATGACTTCGTACAAAACTCGCTTCGAAAGCTTCACTTAAATTTTGTAAGCGATGCTTAC

>NZ_LN831776|55|56|5379342-5379430|CRISPRCasFinder
CTTAAAGTTTTGTAAGCGATGCTTAC	AGATATGACTTCGTACAAAACTCGCTTCGAAAGCTTC
ACTTAAATTTTGTAAGCGATGCTTAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020429641.1|5375662_5376790_-|M20/M25/M40-family-metallo-hydrolase	unknown	unknown	gnl|CDD|349932
NZ_LN831776.1|WP_020426438.1|5389208_5389778_+|thymidine-kinase	unknown	unknown	gnl|CDD|235272
NZ_LN831776.1|WP_046504852.1|5382632_5384054_-|dihydrolipoyl-dehydrogenase	unknown	unknown	gnl|CDD|235660
NZ_LN831776.1|WP_020429632.1|5384220_5384526_+|DUF2627-domain-containing-protein	unknown	unknown	gnl|CDD|378560
NZ_LN831776.1|WP_167345656.1|5388819_5389011_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426440.1|5387055_5388801_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224055
NZ_LN831776.1|WP_020429643.1|5374711_5375284_-|NUDIX-hydrolase	unknown	unknown	gnl|CDD|239516
NZ_LN831776.1|WP_020426437.1|5389924_5390179_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020429646.1|5372329_5372962_-|stage-II-sporulation-protein-M	unknown	unknown	gnl|CDD|131878
NZ_LN831776.1|WP_020426441.1|5385227_5387075_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224055
NZ_LN831776.1|WP_020429645.1|5373370_5373526_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426436.1|5390235_5390754_-|DinB-family-protein	unknown	unknown	gnl|CDD|378981
NZ_LN831776.1|WP_020429647.1|5371642_5372110_-|transcriptional-repressor	unknown	unknown	gnl|CDD|223806
NZ_LN831776.1|WP_046504847.1|5377843_5379331_-|2-oxo-acid-dehydrogenase-subunit-E2	unknown	unknown	gnl|CDD|237001
NZ_LN831776.1|WP_020429635.1|5381284_5382316_-|thiamine-pyrophosphate-dependent-dehydrogenase-E1-component-subunit-alpha	unknown	unknown	gnl|CDD|223997
NZ_LN831776.1|WP_025706662.1|5380294_5381281_-|alpha-ketoacid-dehydrogenase-subunit-beta	unknown	unknown	gnl|CDD|223101
NZ_LN831776.1|WP_020429640.1|5376886_5376988_+|stressosome-associated-protein-Prli42	unknown	unknown	unknown
NZ_LN831776.1|WP_020429639.1|5377067_5377790_-|lipoyl(octanoyl)-transferase-LipB	unknown	unknown	gnl|CDD|319743
NZ_LN831776.1|WP_020429642.1|5375361_5375535_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020429644.1|5373527_5374721_-|hypothetical-protein	unknown	unknown	gnl|CDD|224297

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020429641.1|5375662_5376790_-|M20/M25/M40-family-metallo-hydrolase	gnl|CDD|349932	cd05683, M20_peptT_like, M20 Peptidase T like enzymes specifically cleave tripeptides. Peptidase M20 family, PeptT (tripeptide aminopeptidase; tripeptidase)-like subfamily. This group includes bacterial tripeptidases as well as predicted tripeptidases. Peptidase T acts only on tripeptide substrates, and is thus called a tripeptidase. It catalyzes the release of N-terminal amino acids with hydrophobic side chains from tripeptides with high specificity; dipeptides, tetrapeptides or tripeptides with the N-terminus blocked are not cleaved. Tripeptidases are known to function at the final stage of proteolysis in lactococcal bacteria and release amino acids from tripeptides produced during the digestion of milk proteins such as casein.	0
NZ_LN831776.1|WP_020426438.1|5389208_5389778_+|thymidine-kinase	gnl|CDD|235272	PRK04296, PRK04296, thymidine kinase; Provisional.	4.52186e-110
NZ_LN831776.1|WP_020429632.1|5384220_5384526_+|DUF2627-domain-containing-protein	gnl|CDD|378560	pfam11118, DUF2627, Protein of unknown function (DUF2627). This family is conserved in the Bacillaceae family. Several members are named as YqzF. The function is not known.	2.77949e-29
NZ_LN831776.1|WP_020426440.1|5387055_5388801_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	2.65843e-150
NZ_LN831776.1|WP_020429643.1|5374711_5375284_-|NUDIX-hydrolase	gnl|CDD|239516	cd03424, ADPRase_NUDT5, ADP-ribose pyrophosphatase (ADPRase) catalyzes the hydrolysis of ADP-ribose and a variety of additional ADP-sugar conjugates to AMP and ribose-5-phosphate. Like other members of the Nudix hydrolase superfamily, it requires a divalent cation, such as Mg2+, for its activity. It also contains a highly conserved 23-residue Nudix motif (GX5EX7REUXEEXGU, where U = I, L or V) which functions as a metal binding site/catalytic site. In addition to the Nudix motif, there are additional conserved amino acid residues, distal from the signature sequence, that correlate with substrate specificity. In humans, there are four distinct ADPRase activities, three putative cytosolic enzymes (ADPRase-I, -II, and -Mn) and a single mitochondrial enzyme (ADPRase-m). Human ADPRase-II is also referred to as NUDT5. It lacks the N-terminal target sequence unique to mitochondrial ADPRase. The different cytosolic types are distinguished by their specificities for substrate and specific requirement for metal ions. NUDT5 forms a homodimer.	2.96177e-52
NZ_LN831776.1|WP_046504852.1|5382632_5384054_-|dihydrolipoyl-dehydrogenase	gnl|CDD|235660	PRK05976, PRK05976, dihydrolipoamide dehydrogenase; Validated.	0
NZ_LN831776.1|WP_020426441.1|5385227_5387075_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	0
NZ_LN831776.1|WP_020429646.1|5372329_5372962_-|stage-II-sporulation-protein-M	gnl|CDD|131878	TIGR02831, Stage_II_sporulation_protein_M, stage II sporulation protein M. A comparative genome analysis of all sequenced genomes of shows a number of proteins conserved strictly among the endospore-forming subset of the Firmicutes. This predicted integral membrane protein is designated stage II sporulation protein M. [Cellular processes, Sporulation and germination].	2.65014e-48
NZ_LN831776.1|WP_020426436.1|5390235_5390754_-|DinB-family-protein	gnl|CDD|378981	pfam12867, DinB_2, DinB superfamily. The DinB family are an uncharacterized family of potential enzymes. The structure of these proteins is composed of a four helix bundle.	4.47655e-16
NZ_LN831776.1|WP_020429635.1|5381284_5382316_-|thiamine-pyrophosphate-dependent-dehydrogenase-E1-component-subunit-alpha	gnl|CDD|223997	COG1071, AcoA, Pyruvate/2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit [Energy production and conversion].	4.96243e-146
NZ_LN831776.1|WP_025706662.1|5380294_5381281_-|alpha-ketoacid-dehydrogenase-subunit-beta	gnl|CDD|223101	COG0022, AcoB, Pyruvate/2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit [Energy production and conversion].	0
NZ_LN831776.1|WP_020429644.1|5373527_5374721_-|hypothetical-protein	gnl|CDD|224297	COG1379, COG1379, PHP family phosphoesterase with a Zn ribbon [General function prediction only].	4.7539e-111
NZ_LN831776.1|WP_020429639.1|5377067_5377790_-|lipoyl(octanoyl)-transferase-LipB	gnl|CDD|319743	cd16444, LipB, lipoyl/octanoyl transferase. Lipoate-protein ligase B is a octanoyl-[acyl carrier protein]-protein acyltransferase the catalyzes the first step of lipoic acid synthesis. It transfers endogenous octanoic acid attached via a thioester bond to acyl carrier protein (ACP) onto lipoyl domains, which is later converted by lipoate synthase LipA into lipoylated derivatives.	4.49386e-82
NZ_LN831776.1|WP_046504847.1|5377843_5379331_-|2-oxo-acid-dehydrogenase-subunit-E2	gnl|CDD|237001	PRK11856, PRK11856, branched-chain alpha-keto acid dehydrogenase subunit E2; Reviewed.	1.86848e-140
NZ_LN831776.1|WP_020429647.1|5371642_5372110_-|transcriptional-repressor	gnl|CDD|223806	COG0735, Fur, Fe2+/Zn2+ uptake regulation proteins [Inorganic ion transport and metabolism].	9.80522e-48

Protein sequences

>NZ_LN831776.1|WP_046504847.1|5377843_5379331_-|2-oxo-acid-dehydrogenase-subunit-E2
MSDNTKLTDVIMPQLAESLVSATIGKWLKQPGDAIEQYEPLCDLITDKVNAELPATVDGTLVELLAEEGQTVSVGEVIARIAVAAPAAPSAPAATAAGAPAAAPAPTAQASSRPAASRPAALSPAPAAGRPAAPAAAFDASAPMRSRYSPAVQSLAAEHGIELTAVPGTGLGGRITRKDVLTFLDNGGAAAAVATAAPVPAAGTAAVPAASAGQQAPEALQQPAFQVIQEEVQEALEPVRHSGLHLSETPRIPTIEVEGGRGSSSEYLIDVTPIRNTIATRMRQSVSEIPHAWTMIEVDVTNLVILRNKLKDEFKRKEGINLTYLAFLMKAVVSAIKDYPIMNSVWAVDKIIVKRDINISLAVGTEDSVMTPVIKKADQKNVAGLAREIDELAMKTREGKLRLEDMQGGTFTVNNTGSFGSILSYPIINYPQAAILTFESIVKKPVVINDMIAVRSMANICLSLDHRILDGVICGRFLQRIKDNVEGYTPDTKLY
>NZ_LN831776.1|WP_020429639.1|5377067_5377790_-|lipoyl(octanoyl)-transferase-LipB
MSSTELSLLEISYLPLIEYGAAWELQKAAVQAIDAGTGPERLILLQHPPTYTIGSQHHPEHLLLSAEQLKEKGIALFEIDRGGDITYHGPGQLVGYPLLKLGMDGKVDLHGYLRRLEAVIIDFLASYGIEGSRKPEYTGVWVGDQKICAIGVKFNKSKHRRGFITSHGFAFNVTAGIGERGFQGIIPCGIAEYGVTSLEECAGRSFELGEVARELVPCFLKHFPYEAAAAVEPTDVLQTD
>NZ_LN831776.1|WP_020429640.1|5376886_5376988_+|stressosome-associated-protein-Prli42
MQRQKWFRIVIYVMLLAMIASTVLFVLEPFLAG
>NZ_LN831776.1|WP_020429641.1|5375662_5376790_-|M20/M25/M40-family-metallo-hydrolase
MISQERLIQEFMELVRVDSETGNERQIADVLIEKFGALGLTAIEDDSRERTGHGAGNLFVTWPAEEGTAAPKLLFTCHMDTVVPGKNIQPSLGEDGWITSDGSTILGSDDKAGLAALFEAIRVIQEQKLAHGQIQFVITAGEESGLLGARNMDPSHLDAEFGFALDSNGEVGAIAVAAPAQAKVTMQIFGKSAHAGVNPEDGISAIQVASKAISAMKLGRIDNETTANIGKFAGGGPTNVVCDHVQLDAEARSIVQEKVELQIASMREALETTAREYGAESEFRSEIIYPAFSFNEHDPVVQLAERAITSMGLTPRRFPSGGGSDANVFNGLKVPTVNLAVGYENIHTTKERIKAGDIVKVAELVVAIVKESVKG
>NZ_LN831776.1|WP_020429642.1|5375361_5375535_+|hypothetical-protein
MNDILVRTSSSAVTMVGKPEQIRAVMAGWIKQYGRDMPLAYILMLHSESRNSASKAG
>NZ_LN831776.1|WP_020429643.1|5374711_5375284_-|NUDIX-hydrolase
MKKDEITRNPALDEETLSTKPIFVGKIISLQVDTVKLPDGNTATREVVKHPGAVAVLALNQGKMLVVEQYRQPMHRTEVEIPAGKLDPGEDPLAAAGRELQEETGFHSGELKLLKSFYTSPGFADEIIHLYVTDNAQPGDMALDEDEFLEVSELTLEEAYQYIADGRIADAKTMMAVYAWHLFTLTGQWH
>NZ_LN831776.1|WP_020429644.1|5373527_5374721_-|hypothetical-protein
MALGAKLRSYYCDLHVHIGRTSAGQAVKISGSSSLTFAGIAKEAAQRKGMELIGIIDSHAPGVLADIRALLASGEMSEAEGGGIAYQGTTIVLGTEIEIREPGRKECHVLAFLPDLAAMEDFSSWMGKHMRNINLSSQRLYVPARDLQDEICGRGGILIPAHIFTPHKGLYGCTAERMAELFDLERIAAVELGLSADSEMAGYISELDPFTFLTNSDAHSLGKIGREYNVIEMEKPSFNELKLALARQEGRRVSGNFGLNPRLGKYHRTYCAGCGSIVDEAYATSERCPYCGSQKLVQGVFDRILVIADREQPLIPAHRPPYHYQVPLEFIPGLGKRKLEALLAAFGTEMRILHAAGEAELAAVAGAELAAHIVKARSGTLELSSGGGGTYGKVVKG
>NZ_LN831776.1|WP_020429645.1|5373370_5373526_-|hypothetical-protein
MELFHEQVYLLRVRQLFVSSAEMPLLRPLAGIRRNNGGDSVVKTLPEGNVQ
>NZ_LN831776.1|WP_020429646.1|5372329_5372962_-|stage-II-sporulation-protein-M
MRSLRLMMKEQTPLYIFVAVLFLVGVVFGALIVSALTLDQQQELGDYLGNFFVTVDQQGLPAAPDSYWDIAALNLKWIALIWILGLSVIGLPGILILDFLKGVLIGFTVGCMVSEYSWHGMLFALVSVAPHNLVLIPVLLVGSAAAIAFSLLMIRSRVLGQRRSPVTRPFVMYTVLSFGLAVLVLGISGFEAWVTPTMMRWVTPLLVSKG
>NZ_LN831776.1|WP_020429647.1|5371642_5372110_-|transcriptional-repressor
MEARIDKIKQQLQSQGYKLTPQREATLRVLLENEEDHLSAEDVFMLVKEKAPEIGLATVYRTLELLSELHVVEKINFGDGVARYDLRTDTAKHHHHHLICVQCGTMDEIREDWLGPLEERLEKEFNFTVLDHRLDFHGICYRCKDKNNTDSNPSE
>NZ_LN831776.1|WP_025706662.1|5380294_5381281_-|alpha-ketoacid-dehydrogenase-subunit-beta
MAIMEYIDAIRLAMKEEMERDESVFVLGEDVGVKGGVFTTTKGLQEQFGEERVMDTPLAESAIAGVAIGAAMYGMKPIAEMQYSDFMLPATNQIISEAAKIRYRSNNDWSCPVVIRAPIGGGIFGGLYHSQCPESIFFGTPGLKIVAPYSAYDAKGLLKAAVRDPDPVLFFENKKCYKLIKEDVPEGDYTVPIGEANLLREGSDITVIGYSLPLHFAMQAAEELEREEGITAHILDLRTLQPLDREAIIAAARQTGKVLIVHEDNKTGGIGGEVAAIIAEHCLFELDAPIFRLCGPDVPAMPISPPMEKFFMLSKDKVKAEMLRLAQY
>NZ_LN831776.1|WP_020429635.1|5381284_5382316_-|thiamine-pyrophosphate-dependent-dehydrogenase-E1-component-subunit-alpha
MESQGTVETINRHKPLGLSDGQVIDMYRTMQLGRKYDERSLLLQRAGKINFHVSGIGQEAAQVAAAFALDRENDYFLPYYRDYAFVLSVGMTTRELMLSVFAKAEDPNSGGRQMPGHFGSKRLRIVTGSSPVTTQVPHAVGFALAAKMQKKKFVSFVTFGEGSSNQGDFHEACNFAGVNKLPVIIFCQNNQYAISVPAHKQLGGKVSDRALGYGFPGVRVDGNDPLEVYRVVKEARERALAGEGPTLIEAMMYRLSPHSTSDNDLAYRTKEEVDANWAKDGIAAFRSYLTELGLWSDEQESDLAAEYNLELKAAIEYAENAPFPKPEDTLLHVYSESDLKGGA
>NZ_LN831776.1|WP_046504852.1|5382632_5384054_-|dihydrolipoyl-dehydrogenase
MTISCDVAILGGGTGGYVAAIRAAQLGKSVVVIEMDKLGGTCLHRGCIPSKSLLRSAEVYAEIQESESYGIETAGVQLVFPKVQARKEAVVEQLHQGVQFLMRKNKIQVLKGKGRIIGPSIFSPRSGAVAVELENGEMETVVSGNLIVATGSRPRVLPGLKPDGKVILSSEEALTLEELPASIIIVGGGVIGVEWASMLADFGVQVTVVEAAGQLLPLEDEEIARELLRLLKKRGVKVLTGTTVDAGTCVITESEVTIEARKGEQTQSLSAEKLLVSVGRVANIENIGLENTDIHFGKGVIEVNDNMQTNEPHIYAIGDCIGGLQLAHAASHEGIRAVDHLAGETLHPYHPHLVPRCVYTRPEVASVGYTEKEARALGADVVTGKFPFSAIGKAIVYGMKDGFVKVVADRSSGDILGVQMIGPHVTDLIGEAALAQLLDATPWEIGEAVHAHPTLSEIIGEAMLAVDGRAIGF
>NZ_LN831776.1|WP_020429632.1|5384220_5384526_+|DUF2627-domain-containing-protein
MKLLTTRFIAILILVVPGLLAMKGFLMMKDDIFNYISMHGDETATPVFAWLHFGGGLLLFLAGMSFLGGWILTRDRKRNYVGPRFREKQKTQQPPSPDATS
>NZ_LN831776.1|WP_020426441.1|5385227_5387075_-|ABC-transporter-ATP-binding-protein
MFKALLEPFRHPRLNVGLGDAASFGSPGGRKPKAKAKDWSATLRRIWSYLAKRKAKLVLVLVMVLLSSGLALLGPYLISRAVDHYLEGDGGRTWGIFLITLAVVYLLNSLTSWLQNIWMIEIAQETVYRMRTDLFAHLHRLPISFFNRRQQGEIMSRLTNDIENISSTLNSSAIQIFSSVLTLLGTVGVMLWLSPLLTLLTFIVVPLMILGMRWITRRTGPLFKERQRNMGELNGFIEETLSGQRIIKAFSQEERVISGFRERNARIMLSGYWAQAISGFIPKLMNGLNNLSFAIVAGVGGLLAIRGLVTVGVIIAFVEYTRQFTRPLNDLANQWNTLLSAIAGAERVFEVLDEEAEAKDEGAAVSLDHVEGTVKFSGVSFSYDGGADTLQDISFEAKPGEMIALVGPTGAGKTTLIGLLSRFYDPDKGSITLDGRELSSIRRESLRSHMAFVLQDSFLFKGTIRDNIRYGRLDASDEEVEAAAKLANAHSFIMRMKGGYERMLSVDGSGISQGQKQLLAIARAILANPSMLVLDEATSSIDTVTEIKIQEGLQTLMKGRTSFVIAHRLGTIRAADRILVLQGGRLLQQGSHEELLQEGGLYSELVRGSSDSAAG
>NZ_LN831776.1|WP_020426440.1|5387055_5388801_-|ABC-transporter-ATP-binding-protein
MNIIFSYLKTYRAAAIAALLMMVIELAVELSQPLLISRIIDDGIRAQDNRIVWLWGGVLVVSAVLAFIAGVLSSFFASHASQGFAFDLRDQLYEKVQSFTYAVFSRFTTSSLITRLTADVSQLQDTIFMGLRFMTRVPLVVAGSVVMALVVQVKLGLLLALTLPVLIAFLLWVMKKASVLFRSVQNRLDGVNSVIQENLTGIRLIRVFVRMNHEIARFAAFSGELMKSTVAALRLTETSAPLIMLIVNAGIMLVLWFGRIEISTGEATLGQTVAVINYSLRTIGALSALSWIMATFSRARASSQRIQEVMSADELEAKEMAAVTAREIAPIRGKVEFRQVSFRYPQSDIAVLEDITFKVQPGDRVAIMGATGSGKSSLVGLIPRLYEQSSGDILVDGIPGAEMEISRLRGAIGYVPQEVLLFTGSVRENIAWGHPQATQDEIEQAAMAAQIHETVQELPNGYDTMLGQRGVNLSGGQKQRLTIARALVRKPAVLILDDSTSALDAVTESRLLAELKGMSCTTFLITQKISSTVSADLILLLDEGRLIAQGTHEELMERSELYRKINESQHREGVQHVQSIT
>NZ_LN831776.1|WP_167345656.1|5388819_5389011_-|hypothetical-protein
MEDYTEKIAALQEKGELTAETLSLLMEMLDEMAELNRSNKALRRVILKGQSTMSTRLRDALYE
>NZ_LN831776.1|WP_020426438.1|5389208_5389778_+|thymidine-kinase
MAQLFFKYGAMNSGKSIEILKVAHNYEEQGKSVLIFTPSIDNRDEVGYISSRIGLRKQAIPIDENTDIYSIVSSNLPKPHCVLIDECQFLSKDCILQLVRIVDELNIPVMAFGLKNDFQNNLFEGSKYMLIYADKIEEMKTICWFCERKATMALRVENGKPVYSGKQIQIGGNEAYYPVCRKCHKNPPL
>NZ_LN831776.1|WP_020426437.1|5389924_5390179_-|hypothetical-protein
MGLLKGILHFFIPRERTLVYTTFDQTQYFKIKGRLSAAGIPHRSKINGGMKALGQRAQYGGKATVQHDLFVRKEDEHRAAQAIH
>NZ_LN831776.1|WP_020426436.1|5390235_5390754_-|DinB-family-protein
MNQRPQPGEYSEFPARYISLVPPEGELAAVLREQSNLMYDLLDGLSEEQGSYRYAKGKWSIKQMLGHLTDNDRIMSYRLLAIARGEKAPLPGYEENDYAAAGEFERFTLSEMVQHYKLVRQSTIALLESLPEEAWTRMGAASGNPISVRAVACVIIGHELHHLGVLKERYLK

Crispr_ID: NZ_LN831776_56

• CRISPR_ID: NZ_LN831776_56
• CRISPR_location: 5492359-5492437
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_56

Consensus_repeat	Method
CGGTGCTTTAACAACGGCATTTTTGC	CRISPRCasFinder

spacers of NZ_LN831776_56

>56.1|5492385|27|NZ_LN831776|CRISPRCasFinder
TTTTGTTTCCGGGCAAACCAGCCTTCG

CRISPR arrays and Neighbor proteins around NZ_LN831776_56

CRISPR arrays

The CRISPR arrays of NZ_LN831776_56

>merge|NZ_LN831776|56|5492359-5492437|CRISPRCasFinder
CGGTGCTTTAACAACGGCATTTTTGCTTTTGTTTCCGGGCAAACCAGCCTTCGCGGTGCTTTAACAACGGCATTTTTGC

>NZ_LN831776|56|57|5492359-5492437|CRISPRCasFinder
CGGTGCTTTAACAACGGCATTTTTGC	TTTTGTTTCCGGGCAAACCAGCCTTCG
CGGTGCTTTAACAACGGCATTTTTGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_046504930.1|5494638_5496927_-|5-methyltetrahydropteroyltriglutamate---homocysteine-S-methyltransferase	unknown	unknown	gnl|CDD|235367
NZ_LN831776.1|WP_020429143.1|5494414_5494567_+|DUF1540-domain-containing-protein	unknown	unknown	gnl|CDD|377869
NZ_LN831776.1|WP_020426538.1|5504665_5504944_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426534.1|5500007_5501957_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|376899
NZ_LN831776.1|WP_020429146.1|5490608_5491223_+|VTT-domain-containing-protein	unknown	unknown	gnl|CDD|223475
NZ_LN831776.1|WP_020426533.1|5499369_5499993_-|DedA-family-protein	unknown	unknown	gnl|CDD|223659
NZ_LN831776.1|WP_020426537.1|5504081_5504525_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_LN831776.1|WP_020429149.1|5488761_5489079_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224647
NZ_LN831776.1|WP_039785928.1|5502921_5503959_+|NADH:flavin-oxidoreductase/NADH-oxidase	unknown	unknown	gnl|CDD|239242
NZ_LN831776.1|WP_020429150.1|5487719_5488442_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426535.1|5501931_5502702_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213222
NZ_LN831776.1|WP_046504927.1|5492923_5494066_-|DUF4349-domain-containing-protein	unknown	unknown	gnl|CDD|379526
NZ_LN831776.1|WP_020429151.1|5487072_5487516_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020429148.1|5489174_5489498_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020429154.1|5485031_5485733_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020429147.1|5489524_5490460_-|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_LN831776.1|WP_020426532.1|5498417_5499287_-|undecaprenyl-diphosphate-phosphatase	unknown	unknown	gnl|CDD|234712
NZ_LN831776.1|WP_020429153.1|5485903_5486635_-|iron-sulfur-cluster-repair-di-iron-protein	unknown	unknown	gnl|CDD|274701
NZ_LN831776.1|WP_020429145.1|5491324_5492311_+|peptide-methionine-(R)-S-oxide-reductase-MsrB	unknown	unknown	gnl|CDD|184456
NZ_LN831776.1|WP_020429152.1|5486870_5487086_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224393

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020426534.1|5500007_5501957_-|FtsX-like-permease-family-protein	gnl|CDD|376899	pfam02687, FtsX, FtsX-like permease family. This is a family of predicted permeases and hypothetical transmembrane proteins. Buchnera aphidicola LolC has been shown to transport lipids targeted to the outer membrane across the inner membrane. Both LolC and Streptococcus cristatus TptD have been shown to require ATP. This region contains three transmembrane helices.	1.978e-06
NZ_LN831776.1|WP_020429152.1|5486870_5487086_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|224393	COG1476, COG1476, Predicted transcriptional regulators [Transcription].	1.96038e-23
NZ_LN831776.1|WP_020426533.1|5499369_5499993_-|DedA-family-protein	gnl|CDD|223659	COG0586, DedA, Uncharacterized membrane-associated protein [Function unknown].	1.11905e-46
NZ_LN831776.1|WP_020426537.1|5504081_5504525_+|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	1.10107e-10
NZ_LN831776.1|WP_020429149.1|5488761_5489079_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	6.73645e-34
NZ_LN831776.1|WP_046504930.1|5494638_5496927_-|5-methyltetrahydropteroyltriglutamate---homocysteine-S-methyltransferase	gnl|CDD|235367	PRK05222, PRK05222, 5-methyltetrahydropteroyltriglutamate--homocysteine S-methyltransferase; Provisional.	0
NZ_LN831776.1|WP_020426535.1|5501931_5502702_-|ABC-transporter-ATP-binding-protein	gnl|CDD|213222	cd03255, ABC_MJ0796_LolCDE_FtsE, ATP-binding cassette domain of the transporters involved in export of lipoprotein and macrolide, and cell division protein. This family is comprised of MJ0796 ATP-binding cassette, macrolide-specific ABC-type efflux carrier (MacAB), and proteins involved in cell division (FtsE), and release of lipoproteins from the cytoplasmic membrane (LolCDE). They are clustered together phylogenetically. MacAB is an exporter that confers resistance to macrolides, while the LolCDE system is not a transporter at all. An FtsE null mutants showed filamentous growth and appeared viable on high salt medium only, indicating a role for FtsE in cell division and/or salt transport. The LolCDE complex catalyzes the release of lipoproteins from the cytoplasmic membrane prior to their targeting to the outer membrane.	3.0386e-105
NZ_LN831776.1|WP_046504927.1|5492923_5494066_-|DUF4349-domain-containing-protein	gnl|CDD|379526	pfam14257, DUF4349, Domain of unknown function (DUF4349). This family of proteins is found in bacteria and archaea. Proteins in this family are typically between 282 and 353 amino acids in length. There is a single completely conserved residue D that may be functionally important.	5.20136e-60
NZ_LN831776.1|WP_020429146.1|5490608_5491223_+|VTT-domain-containing-protein	gnl|CDD|223475	COG0398, COG0398, Uncharacterized conserved protein [Function unknown].	2.35097e-16
NZ_LN831776.1|WP_039785928.1|5502921_5503959_+|NADH:flavin-oxidoreductase/NADH-oxidase	gnl|CDD|239242	cd02932, OYE_YqiM_FMN, Old yellow enzyme (OYE) YqjM-like FMN binding domain. YqjM is involved in the oxidative stress response of Bacillus subtilis. Like the other OYE members, each monomer of YqjM contains FMN as a non-covalently bound cofactor and uses NADPH as a reducing agent. The YqjM enzyme exists as a homotetramer that is assembled as a dimer of catalytically dependent dimers, while other OYE members exist only as monomers or dimers. Moreover, the protein displays a shared active site architecture where an arginine finger at the COOH terminus of one monomer extends into the active site of the adjacent monomer and is directly involved in substrate recognition. Another remarkable difference in the binding of the ligand in YqjM is represented by the contribution of the NH2-terminal tyrosine instead of a COOH-terminal tyrosine in OYE and its homologs.	4.57596e-168
NZ_LN831776.1|WP_020429143.1|5494414_5494567_+|DUF1540-domain-containing-protein	gnl|CDD|377869	pfam07561, DUF1540, Domain of Unknown Function (DUF1540). This family has four conserved cysteines, which is suggestive of a metal binding function.	2.06674e-08
NZ_LN831776.1|WP_020429147.1|5489524_5490460_-|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	6.37247e-46
NZ_LN831776.1|WP_020426532.1|5498417_5499287_-|undecaprenyl-diphosphate-phosphatase	gnl|CDD|234712	PRK00281, PRK00281, undecaprenyl-diphosphate phosphatase.	3.04427e-105
NZ_LN831776.1|WP_020429153.1|5485903_5486635_-|iron-sulfur-cluster-repair-di-iron-protein	gnl|CDD|274701	TIGR03652, FeS_repair_RIC, iron-sulfur cluster repair di-iron protein. Members of this protein family, designated variously as YftE, NorA, DrnN, and NipC, are di-iron proteins involved in the repair of iron-sulfur clusters. Previously assigned names reflect pleiotropic effects of damage from NO or other oxidative stress when this protein is mutated. The suggested name now is RIC, for Repair of Iron Centers. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	3.92093e-85
NZ_LN831776.1|WP_020429145.1|5491324_5492311_+|peptide-methionine-(R)-S-oxide-reductase-MsrB	gnl|CDD|184456	PRK14018, PRK14018, bifunctional peptide-methionine (S)-S-oxide reductase MsrA/peptide-methionine (R)-S-oxide reductase MsrB.	2.55812e-106

Protein sequences

>NZ_LN831776.1|WP_020429145.1|5491324_5492311_+|peptide-methionine-(R)-S-oxide-reductase-MsrB
MSDIQADNISGKTEKATFAGGCFWCMVSPFEELPGIVEVVSGYTGGHTVNPTYEEVCSETTGHVEAVQITFQPDIFPYTKLLELFWQQIDPTDAGGQFYDRGTSYGTAIFTHSEEQRQQAEASKAALQASGRFSAPIVTPILPAKPFYRAEEYHQGYHHKNPGHYKRYRQGSGRDAFIESHWKHKEDKASLKERLTPLQYEVTQNNATESPFRNEFWDHHGEGIYVDIVSGEPLFSSQDKFDSGCGWPSFTRPIRDYSVKEKTDLSHLMIRTEVRSKTADSHLGHVFNDGPGPNGLRYCINSAALRFVPKEDLEKEGYGEYRALFQHA
>NZ_LN831776.1|WP_020429146.1|5490608_5491223_+|VTT-domain-containing-protein
MRKWLTVLLYVSGIFLAFIYRYDILAWLRQDHNAFLGLSAAALLALFPVVPYKLIIGIYGYAYGSLTAALICWSASTLAGAVIYAVVKYMFKEKAGKYLTSVSALGKFTSAVQRRPFAAVVLARLVPVIPQMGVNIYAGAAGLPFWSYLAASGLGKIPGIALYAFLGGQLFDHPRNGLIAVLVYVVVLALAVLALRPRSLWTKE
>NZ_LN831776.1|WP_020429147.1|5489524_5490460_-|Gfo/Idh/MocA-family-oxidoreductase
MKITGRTKVAIVGLGDIARKVYLPLLSRHDQVEVVGVLSHSPSTVQGVVHSYRFPRGTTDLKELLSWGPDAVFVHSPTPTHYDIVMKCLNHGIPVYVDKPLSYDLEESRRMAGFAEEKGLLLGVGFNRRFAPMYTAAKAWLDTTGGISACQAFKHRTRLQSGSSRETVHDDLIHILDLLLWLCGEDAELLHSSLKADDAGRMLQSSGMLGWSQGATGMYSMVRDAGADLEKLELHGNGRSAEVADMEQATLYETGSLPRIQHFGSWDTVLERRGFSGAVNHFLNSIDTPLQCGISASAVLSSHELAAKLAD
>NZ_LN831776.1|WP_020429148.1|5489174_5489498_-|hypothetical-protein
MDDYRKSTEEQIIESYKRDEEMMILVFAQWCVNNKLDPHALYLEAYPQQEGNAALSHALSLTVPIDEAGFISDDTVLGVLSLYSNDDLAYVVSEAIAGRKTRQDSEG
>NZ_LN831776.1|WP_020429149.1|5488761_5489079_-|helix-turn-helix-transcriptional-regulator
MEEHQLTMCPRFESAFSFLGKRWNGLIIQTLMSGPKRFKDISGLIPSMSDKMLSERMKDLECEGILVRHVYPETPVRIEYELTAKGRALEPVMQQIQSWAESWVE
>NZ_LN831776.1|WP_020429150.1|5487719_5488442_-|hypothetical-protein
MTTTLFSREITYGKKDVAELESASIRVQLIYDKVLFMLHSHLPDSLWNDWIGVPYEIISSLYKGDNDSGSVFQKWIQSEAGWKCIGCERHCLEPSAGPAFPSSRQQRRFTYHNGIRQSMVLQAVIWSMYENTVLFQPYLGEEAFLNEADLDTISTYFVPTYLSKQRLTENGKRCKEYQESNIRVYQEWIAAPDLVLQWNGGLTEGRWMTGVYVDHSRFAGLGPYLKDAQGKRTYMRANVK
>NZ_LN831776.1|WP_020429151.1|5487072_5487516_+|hypothetical-protein
MGRTNLDERQLQNKHKAGNQAFILLAFLLLADMGLQNYGIHWLEYPMSNYVIFLIGVGSYLVRIIWNGSYAGPGSGNLTANGRSILGAVLAILVALCVITAAWMGSTGKSSHGTGTGPAILMISTAVGLIILGTVFWIRRRNNRDEA
>NZ_LN831776.1|WP_020429152.1|5486870_5487086_+|helix-turn-helix-transcriptional-regulator
MGKNLRLKASRAAKDMSQKQLADAVGVTRQTIIAIENGDYNPTIRLCIEICLTLGKTLDELFWEGDKHGEN
>NZ_LN831776.1|WP_020429153.1|5485903_5486635_-|iron-sulfur-cluster-repair-di-iron-protein
MTAKQLNNTVTEGSVHFSGEAMVRDIVLQFPKAADYFKAQRIDFCCGGAKPLVEAAAEKGLDTGAVLQDLNKLLAEHPVLEEDSAWNEASSEELADYIINKHHRYLREELPLIAQNVTKVFRVHGEDSPHLAEVYRLFHTLREELLEHTAKEEESEFPKMLAYEKNPTEDGLTELRGLLRTLEAEHDGAGDILRELRRVTNDYTPPEHACTTYRLTYARLEELEGMTFEHVHLENNILFLRYQ
>NZ_LN831776.1|WP_020429154.1|5485031_5485733_-|hypothetical-protein
MSAKWVWRIWLGILIIAVTGGCSSVLDAQNEGNNGGAGNAGPAFSVRVGDSELAGSSGGQISEAYKDGMPLIELLKRSGVATLAEDGNSLLTVNKVSLSPEWIWGIQLNGKKILDWNSSVDRSDSILIAAEPKAAGAEQQPVIFTVNGGSEQPEMTHSYVLPYSEDLSVRGVLKSSGMVLLAEDNKTVISIMDYKPLSNEAWTLKVNGKQLLDSGIDMKLRPQDTLEVALVLR
>NZ_LN831776.1|WP_046504927.1|5492923_5494066_-|DUF4349-domain-containing-protein
MQKRGLHYLYYLLGLLMFAVVVAGCGSGGNNDAAGNSLMKADTASTEASVDGGAAQNASADVAEQSMASKAEAPAAEGTKAGGGNSAVGSTDAAQTSKGTAGFTGSDVVAGLNKKLIYHANLTMEVKDYAAAQTEVRNMVTLANGYIIEFSESTSGYERGGTFILKVPASGFSSFLSSLEKIKNEKLQRQIQGQDVSEEYVDLESRLKAKQLMESQYIEFMKKATKSADLVAFANQLGAIQEEIETIKGRMRYIDQNVSFSTVELRLYQTDESLNITKAKEQGPLMNRASEALQGSLHALSVMFQWIIIFLAAAFPVLIIAAIVVLIVLWFRRKAKPRDRGRADRMQMANRELKQPLPLPQKPDEQPAQVEGELEDRKPE
>NZ_LN831776.1|WP_020429143.1|5494414_5494567_+|DUF1540-domain-containing-protein
MAKDVQCAVNSCTYWAEENKCNAESIFVAYHSSKQPSNAEETDCKTFERK
>NZ_LN831776.1|WP_046504930.1|5494638_5496927_-|5-methyltetrahydropteroyltriglutamate---homocysteine-S-methyltransferase
MTNKITTSNLGYPRIGKNREWKKTLEAYWSGKIDEQDFLAQMAGIQLQHLQSQQKAGIDLIPVNDFTFYDHVLDTAVMFGIIPQRYAYNGGAVPLDLYFAMARGNASAPACEMTKWFNTNYHYIVPEIGSLTPQLTENKPLAAYRFAKTQAGIEGKPVIVGLYTFLKLSKGFPAAEIGEVAERFLPVYIQLLQELEQEGVAWVQIDEPAVVTGLTPEEIALLKTIYGAISAAVPGLKLILQTYFEAAEPLEALLELPVQAIGLDFVHDGGVNLEAIERLGWPAGKLLGAGIIDGRSIWRADPDAKLGLIQKLAAHVPLDRLILQPSSSLLHVPVTVQSEGKLKPAVKQALAFADEKLAELGLLAAAAGGGNSNAAAQLAESREALAAFRALPERGRQDVAEQVRRLDALPDSRSLPFAERVKLQQAKWKLPLLPTTTIGSFPQTAEVRQARLKWRKGVWNEERYDTFVRRQIAEAITLQEELGLDVLVHGEFERTDMVEFFGEKLAGYLFTQNGWVQSYGSRCVKPPVIYADVAFIQPMTVKESVYAQSLTRLPVKGMLTGPVTILNWSFVRDDLSREEVAKQIALALRHEVQALEDAGIEMIQVDEPAIREGLPLKAEDHAHYLNWAVRSFRVATNHVKDTTQVHTHMCYSEFNDMIGAISAMDADVISIETSRSHGELIAAFEEDDYDKGIGLGVYDIHSPRVPEVEEMTHNIERALRVLDAGQFWINPDCGLKTRGWEETEAALRNMVLAAANVRKNNA
>NZ_LN831776.1|WP_020426532.1|5498417_5499287_-|undecaprenyl-diphosphate-phosphatase
MELLTIIKAIILGIVEGLTEFAPVSSTGHMIIVDDMWLKSQEFLGKYAANTFKVVIQLGSILAVVVIFRNRFIDLLGLKRFSRKELTAVPEGQPAVETTGRLKLAQVIVGLIPAGVLGFLFEDYIDEHLFSTSTVLIGLVVGAILMICADLLAPKKIKTESVDQITYRQALSVGLIQCLSLWPGFSRSGSTISGGVLLGMSHRAAADFTFIMAVPIMAGASLISLLKNWQYFTLDDLPFFIAGFISAFLFALLSMRFFLKLINRIKLMPFAIYRIILAAVVYFVWFYIS
>NZ_LN831776.1|WP_020426533.1|5499369_5499993_-|DedA-family-protein
MKTWITDIMEQFGYAGIFLMLALENIFPPIPSEVILPFGGFMTTTSGLTIPGVLIASTAGSLLGAAILYWIGRLLEVSRMERIVDRYGKWIRIKKSDIRKADAWFDKYGYWTVLFCRMVPLVRSLISIPAGMSGMKFGLFMLFTTIGTLGWNTLLILLGAALGESWEDIGGYIGTYSSIVYILLAGGILVLGLLYLRKRHTEGKARG
>NZ_LN831776.1|WP_020426534.1|5500007_5501957_-|FtsX-like-permease-family-protein
MTFRQFAYRNVARNKRKYAAYFVSSAFSVMVFFLCALFIYHPAISRDMILGTAADTMMAAEGIIYVFCSLFVLVSVGSFLQSRKLEFGILLMHGMTKRQLKLMVFLENMMIGGSAILTGTLLGLLLGKLFLMIGSGFLGIEPLEFHLSWQAPVLTICSFVLLFMLISLLTFAFIGNESPRGLFRGGGRGEAEPEVSGGLALLAGLLLLAGYGLAAVTTAATIEIMMFPVVLITICGTYLFYTQLSLYIVGMLRKLRRFYWKHTHILTFAGLSYRWKDNGRMFFMVTIVSAVSFTSVGVFASIHTLSRELKLDYPAAVGYVAKGGGYASSEKRDLQGITAALERLGLPYETLRIPLKYAAIVSQTGPDHTKQLPLMSYSNYKLALRHAGFSSDEPPLAGNQGLVMIGSQRDRSLTAARFKATYTLKQGTRIQEIGYTQHVPIAEYLLPELDGRGGGDFSGLVVSDSLYSGIVPVHQDWYTGFYMEDFPRTAGIAPELAATGKVPYEAKSSYAVVISGTLFEIQRTLYSTMLFASLLVGTVFFIAAGSFLYFRLYVDLDHDRLQYSTLSKMGLTDRELDRIATLQLALMFFVPVLLAVLHSLFAFIALQRMFYLSIAAETGAVLTGYLAAQTLYFFFIRSRYLRNLKKNLI
>NZ_LN831776.1|WP_020426535.1|5501931_5502702_-|ABC-transporter-ATP-binding-protein
MPILDVHNLSKIYEGKVSIHALNHIRFAVEQGEFVGIMGPSGSGKTTLLNVIATIDEPTSGEVMINGRDPRGLGRKDRALFRRKELGFVFQHFNLLDTLTVEENVVLPLTLAGFTVQEMEYRLGEVADRLGIRALLDKRTNEISGGQMQRVAIARAMIHRPSLILADEPTGSLDSKAAGEVMNLLAEVNGTEGTTVLMVTHDAVAASFCHRVIFIKDGRFHSEMYRGSSRAAFFQNIIDMLSLLGGGGHDLPAVRL
>NZ_LN831776.1|WP_039785928.1|5502921_5503959_+|NADH:flavin-oxidoreductase/NADH-oxidase
MKDLFTPYALQNLKLKNRVVMPPMCQYSVTDKDGIATDWHYNHYVSRAVGGTGLIIMEMTDVDPDGRITDYDLGIWSDEHIPALARIVEACHSYGAKVGIQIAHAGRKAEDAQLPVAPSAIPFSAEYKTPRELTTEEVKAMVQKFQAGVERAVQAGFDVIELHGAHGYLIHQFHSPLTNKRTDEYGKDLTLFGREVIQAAKKVMPEGMPLIMRISAQEYVEGGYGIRESLEIGRAYKEAGADIFHVSAGGEGAIAAEGKPGTHAAYQIPLARAFKQELNVPVIAVGRLDEAVLANAVIGNDEADLVAVGRGMLRNPYWTLEAGVQLGKDAGLPKQYELGFPRSRR
>NZ_LN831776.1|WP_020426537.1|5504081_5504525_+|MarR-family-transcriptional-regulator
MKNPLEGGLITSWLSLTYIQMKVAGELEAKLQETFGWSLNEFYLMYFLSEAPEKKLRLQQLESMVGLSQSAVSRLVSRFEAKGCGALQRTTCDDDRRSIYTSLTPIGQEKLDRAQVTVNEVLFEAFPRTEVKELLEDMLRLKPQQQP
>NZ_LN831776.1|WP_020426538.1|5504665_5504944_+|hypothetical-protein
MLFSVMQLLGGMILSLGWIPQIARILKTKSVADLSLKSYLLMLLGIALMEAYAVNLTLTGAGLAFLITNTLSLCVVSAVIVLILRYAGRSKG

Crispr_ID: NZ_LN831776_57

• CRISPR_ID: NZ_LN831776_57
• CRISPR_location: 5507757-5508038
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 6 spacers

Consensus repeat of NZ_LN831776_57

Consensus_repeat	Method
CGTAGTTGCAGACNTAGG	CRT

spacers of NZ_LN831776_57

>57.1|5507775|30|NZ_LN831776|CRT
TGGAGGTGTAGATGCAGACGTATTTGCAAA
>57.2|5507823|30|NZ_LN831776|CRT
TGCAGACATAAGTGCAGATATAGGTGCAGA
>57.3|5507871|18|NZ_LN831776|CRT
TGCAGATATAGGTGCAGA
>57.4|5507907|30|NZ_LN831776|CRT
TGGAGACATAGGTGCAGACATAGGTGGAGA
>57.5|5507955|30|NZ_LN831776|CRT
TGGAGACATAGGTGCAGACATAGGTGCAGT
>57.6|5508003|18|NZ_LN831776|CRT
TGCAGACGTAGGTGCAGA

CRISPR arrays and Neighbor proteins around NZ_LN831776_57

CRISPR arrays

The CRISPR arrays of NZ_LN831776_57

>merge|NZ_LN831776|57|5507757-5508038|CRT
TGTGGTTGCAGACATAGGTGGAGGTGTAGATGCAGACGTATTTGCAAACGTAGTTGCAGATGTAGTTGCAGACATAAGTGCAGATATAGGTGCAGACGTAGTTGCAGACGTAGGTGCAGATATAGGTGCAGACGTAGTTGCAGACGTAGGTGGAGACATAGGTGCAGACATAGGTGGAGACGTAGTTGCAGACACAGGTGGAGACATAGGTGCAGACATAGGTGCAGTCATAGTTGCAGACGTAGGTGCAGACGTAGGTGCAGACATTGTTGCAGAGCACTG

>NZ_LN831776|57|6|5507757-5508038|CRT
TGTGGTTGCAGACATAGG	TGGAGGTGTAGATGCAGACGTATTTGCAAA
CGTAGTTGCAGATGTAGT	TGCAGACATAAGTGCAGATATAGGTGCAGA
CGTAGTTGCAGACGTAGG	TGCAGATATAGGTGCAGA
CGTAGTTGCAGACGTAGG	TGGAGACATAGGTGCAGACATAGGTGGAGA
CGTAGTTGCAGACACAGG	TGGAGACATAGGTGCAGACATAGGTGCAGT
CATAGTTGCAGACGTAGG	TGCAGACGTAGGTGCAGA
CATTGTTGCAGAGCACTG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020431598.1|5513920_5514793_-|radical-SAM-protein	unknown	unknown	gnl|CDD|100105
NZ_LN831776.1|WP_039790603.1|5511666_5512338_-|membrane-protein	unknown	unknown	gnl|CDD|376838
NZ_LN831776.1|WP_020426534.1|5500007_5501957_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|376899
NZ_LN831776.1|WP_046504936.1|5508132_5508834_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426533.1|5499369_5499993_-|DedA-family-protein	unknown	unknown	gnl|CDD|223659
NZ_LN831776.1|WP_020426538.1|5504665_5504944_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_039785928.1|5502921_5503959_+|NADH:flavin-oxidoreductase/NADH-oxidase	unknown	unknown	gnl|CDD|239242
NZ_LN831776.1|WP_020431612.1|5509457_5510282_+|NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|224995
NZ_LN831776.1|WP_020426541.1|5507009_5507744_+|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|379312
NZ_LN831776.1|WP_020426540.1|5505967_5506666_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_LN831776.1|WP_020431597.1|5514789_5516175_-|STM4012-family-radical-SAM-protein	unknown	unknown	gnl|CDD|181292
NZ_LN831776.1|WP_020431613.1|5509004_5509391_+|MerR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|133398
NZ_LN831776.1|WP_020426539.1|5504991_5505966_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|340424
NZ_LN831776.1|WP_020431596.1|5516211_5516997_-|STM4013/SEN3800-family-hydrolase	unknown	unknown	gnl|CDD|293767
NZ_LN831776.1|WP_020431599.1|5513390_5513924_-|adenylyl-sulfate-kinase	unknown	unknown	gnl|CDD|223603
NZ_LN831776.1|WP_020426537.1|5504081_5504525_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_LN831776.1|WP_020431600.1|5512689_5513190_-|Crp/Fnr-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223736
NZ_LN831776.1|WP_020426532.1|5498417_5499287_-|undecaprenyl-diphosphate-phosphatase	unknown	unknown	gnl|CDD|234712
NZ_LN831776.1|WP_020431611.1|5510644_5511436_-|TIGR00266-family-protein	unknown	unknown	gnl|CDD|376704
NZ_LN831776.1|WP_020426535.1|5501931_5502702_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213222

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_039790603.1|5511666_5512338_-|membrane-protein	gnl|CDD|376838	pfam02588, YitT_membrane, Uncharacterized 5xTM membrane BCR, YitT family COG1284. This is probably a bacterial ABC transporter permease (personal obs:Yeats C).	2.7983e-37
NZ_LN831776.1|WP_020426534.1|5500007_5501957_-|FtsX-like-permease-family-protein	gnl|CDD|376899	pfam02687, FtsX, FtsX-like permease family. This is a family of predicted permeases and hypothetical transmembrane proteins. Buchnera aphidicola LolC has been shown to transport lipids targeted to the outer membrane across the inner membrane. Both LolC and Streptococcus cristatus TptD have been shown to require ATP. This region contains three transmembrane helices.	1.978e-06
NZ_LN831776.1|WP_020426535.1|5501931_5502702_-|ABC-transporter-ATP-binding-protein	gnl|CDD|213222	cd03255, ABC_MJ0796_LolCDE_FtsE, ATP-binding cassette domain of the transporters involved in export of lipoprotein and macrolide, and cell division protein. This family is comprised of MJ0796 ATP-binding cassette, macrolide-specific ABC-type efflux carrier (MacAB), and proteins involved in cell division (FtsE), and release of lipoproteins from the cytoplasmic membrane (LolCDE). They are clustered together phylogenetically. MacAB is an exporter that confers resistance to macrolides, while the LolCDE system is not a transporter at all. An FtsE null mutants showed filamentous growth and appeared viable on high salt medium only, indicating a role for FtsE in cell division and/or salt transport. The LolCDE complex catalyzes the release of lipoproteins from the cytoplasmic membrane prior to their targeting to the outer membrane.	3.0386e-105
NZ_LN831776.1|WP_020426533.1|5499369_5499993_-|DedA-family-protein	gnl|CDD|223659	COG0586, DedA, Uncharacterized membrane-associated protein [Function unknown].	1.11905e-46
NZ_LN831776.1|WP_020426537.1|5504081_5504525_+|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	1.10107e-10
NZ_LN831776.1|WP_020431613.1|5509004_5509391_+|MerR-family-transcriptional-regulator	gnl|CDD|133398	cd04770, HTH_HMRTR, Helix-Turn-Helix DNA binding domain of Heavy Metal Resistance transcription regulators. Helix-turn-helix (HTH) heavy metal resistance transcription regulators (HMRTR): MerR1 (mercury), CueR (copper), CadR (cadmium), PbrR (lead), ZntR (zinc), and other related proteins. These transcription regulators mediate responses to heavy metal stress in eubacteria. They belong to the MerR superfamily of transcription regulators that promote transcription of various stress regulons by reconfiguring the operator sequence located between the -35 and -10 promoter elements. A typical MerR regulator is comprised of two distinct domains that harbor the regulatory (effector-binding) site and the active (DNA-binding) site. Their N-terminal domains are homologous and contain a DNA-binding winged HTH motif, while the C-terminal domains are often dissimilar and bind specific coactivator molecules such as metal ions, drugs, and organic substrates.	5.46756e-29
NZ_LN831776.1|WP_020431598.1|5513920_5514793_-|radical-SAM-protein	gnl|CDD|100105	cd01335, Radical_SAM, Radical SAM superfamily. Enzymes of this family generate radicals by combining a 4Fe-4S cluster and S-adenosylmethionine (SAM) in close proximity. They are characterized by a conserved CxxxCxxC motif, which coordinates the conserved iron-sulfur cluster. Mechanistically, they share the transfer of a single electron from the iron-sulfur cluster to SAM, which leads to its reductive cleavage to methionine and a 5'-deoxyadenosyl radical, which, in turn, abstracts a hydrogen from the appropriately positioned carbon atom. Depending on the enzyme, SAM is consumed during this process or it is restored and reused. Radical SAM enzymes catalyze steps in metabolism, DNA repair, the biosynthesis of vitamins and coenzymes, and the biosynthesis of many antibiotics. Examples are biotin synthase (BioB), lipoyl synthase (LipA), pyruvate formate-lyase (PFL), coproporphyrinogen oxidase (HemN), lysine 2,3-aminomutase (LAM), anaerobic ribonucleotide reductase (ARR), and MoaA, an enzyme of the biosynthesis of molybdopterin.	1.06554e-05
NZ_LN831776.1|WP_020431611.1|5510644_5511436_-|TIGR00266-family-protein	gnl|CDD|376704	pfam01987, AIM24, Mitochondrial biogenesis AIM24. In eukaryotes, this domain is involved in mitochondrial biogenesis. Its function in prokaryotes in unknown.	2.83808e-84
NZ_LN831776.1|WP_020426540.1|5505967_5506666_-|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	1.76906e-72
NZ_LN831776.1|WP_020431597.1|5514789_5516175_-|STM4012-family-radical-SAM-protein	gnl|CDD|181292	PRK08208, PRK08208, coproporphyrinogen III oxidase family protein.	0
NZ_LN831776.1|WP_020431612.1|5509457_5510282_+|NAD(P)-dependent-oxidoreductase	gnl|CDD|224995	COG2084, MmsB, 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases [Lipid metabolism].	5.99906e-64
NZ_LN831776.1|WP_020426539.1|5504991_5505966_-|sensor-histidine-kinase	gnl|CDD|340424	cd16948, HATPase_BceS-YxdK-YvcQ-like, Histidine kinase-like ATPase domain of two-component sensor histidine kinases similar to Bacillus subtilis BceS, YxdK, and Bacillus thuringiensis YvcQ. This family includes the histidine kinase-like ATPase (HATPase) domains of various two-component sensor histidine kinase (HKs) such as Bacillus subtilis BceS and Bacillus thuringiensis YvcQ, the HKs of the two-component regulatory system (TCSs) BceS-BceR and YvcQ-YvcP, repsectively, which are both involved in regulating bacitracin resistance. It also includes the HATPase domain of YxdK, the HK of YxdK-YxdJ TCS involved in sensing antimicrobial compounds.	1.22556e-48
NZ_LN831776.1|WP_020431596.1|5516211_5516997_-|STM4013/SEN3800-family-hydrolase	gnl|CDD|293767	cd16148, sulfatase_like, uncharacterized sulfatase subfamily. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	1.56807e-15
NZ_LN831776.1|WP_020431599.1|5513390_5513924_-|adenylyl-sulfate-kinase	gnl|CDD|223603	COG0529, CysC, Adenylylsulfate kinase and related kinases [Inorganic ion transport and metabolism].	2.71802e-84
NZ_LN831776.1|WP_039785928.1|5502921_5503959_+|NADH:flavin-oxidoreductase/NADH-oxidase	gnl|CDD|239242	cd02932, OYE_YqiM_FMN, Old yellow enzyme (OYE) YqjM-like FMN binding domain. YqjM is involved in the oxidative stress response of Bacillus subtilis. Like the other OYE members, each monomer of YqjM contains FMN as a non-covalently bound cofactor and uses NADPH as a reducing agent. The YqjM enzyme exists as a homotetramer that is assembled as a dimer of catalytically dependent dimers, while other OYE members exist only as monomers or dimers. Moreover, the protein displays a shared active site architecture where an arginine finger at the COOH terminus of one monomer extends into the active site of the adjacent monomer and is directly involved in substrate recognition. Another remarkable difference in the binding of the ligand in YqjM is represented by the contribution of the NH2-terminal tyrosine instead of a COOH-terminal tyrosine in OYE and its homologs.	4.57596e-168
NZ_LN831776.1|WP_020431600.1|5512689_5513190_-|Crp/Fnr-family-transcriptional-regulator	gnl|CDD|223736	COG0664, Crp, cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases [Signal transduction mechanisms].	3.45514e-21
NZ_LN831776.1|WP_020426532.1|5498417_5499287_-|undecaprenyl-diphosphate-phosphatase	gnl|CDD|234712	PRK00281, PRK00281, undecaprenyl-diphosphate phosphatase.	3.04427e-105
NZ_LN831776.1|WP_020426541.1|5507009_5507744_+|class-I-SAM-dependent-methyltransferase	gnl|CDD|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	6.16525e-25

Protein sequences

>NZ_LN831776.1|WP_020426541.1|5507009_5507744_+|class-I-SAM-dependent-methyltransferase
MKQNKYDEAGFFAKYSAMPRSTGGLEAAGEWSTFRSLLPDLHGTRVLDLGCGFGWHCRYAREQQAESVVGIDLSENMLERARAMTDDPGIEYRRGAIEDIRFAAGEFDVVISSLAIHYVERFDLLCCEVQHCLRTGGSFVLSVEHPIYTALAAQDWHYGPDGAKLHWPLDHYHDEGPREARFLEDDVIKYHRNIATYLNTLITSGFTVTKLSELQPTPEMLEQNAAWHEELRRPMFLLLSAVRN
>NZ_LN831776.1|WP_020426540.1|5505967_5506666_-|response-regulator-transcription-factor
MFKIFIIEDDRGLVMLLQDYLHKFGYETQAVHDFEAVRAEFESFAPHLVLLDVNLPKFDGYYWCRQIRGLSTCPILFISAREGKMDQVMALENGADDYITKPFDYEIALAKIKSHLRRAYGSYAGGGTERSLTVAGLMLDVERLVLSRGSAKIDLSHTEAKILDELMQKAGTVVTRDRLLEKIWDDQAFVDDNTLNVYVTRVRKKLAALDIADGLQTVRGQGYRLCENWEEA
>NZ_LN831776.1|WP_020426539.1|5504991_5505966_-|sensor-histidine-kinase
MKLFLREQTPLIVIYLAQLLMITLVYRLDGGSGMNVSLYAGLLSTCLLLAYLAYRYFSNRSFYERLLNLPASLDDSGGPAQSSPLAESLRGVLAHQFRLYQNDLHSYRHKLEEHIHFINQWVHGMKTPLSVIHLIIQDKDGPPFTAIGDELDRLKKGLDTVLYTARLDTFEHDFYVERLELAAIVRGVTSEQKRLFIRKRVFPAIRVENGLFITSDEKWLSFVLTQLITNALRYTVEEGRFVHFHGYAGEQGRPVLEVRDEGVGIPPGDLPRVFDAYFTGVNGRSFQESTGMGLYLVKQICGKLGHQVEISSEVGQGTAVRIIF
>NZ_LN831776.1|WP_020426538.1|5504665_5504944_+|hypothetical-protein
MLFSVMQLLGGMILSLGWIPQIARILKTKSVADLSLKSYLLMLLGIALMEAYAVNLTLTGAGLAFLITNTLSLCVVSAVIVLILRYAGRSKG
>NZ_LN831776.1|WP_020426537.1|5504081_5504525_+|MarR-family-transcriptional-regulator
MKNPLEGGLITSWLSLTYIQMKVAGELEAKLQETFGWSLNEFYLMYFLSEAPEKKLRLQQLESMVGLSQSAVSRLVSRFEAKGCGALQRTTCDDDRRSIYTSLTPIGQEKLDRAQVTVNEVLFEAFPRTEVKELLEDMLRLKPQQQP
>NZ_LN831776.1|WP_039785928.1|5502921_5503959_+|NADH:flavin-oxidoreductase/NADH-oxidase
MKDLFTPYALQNLKLKNRVVMPPMCQYSVTDKDGIATDWHYNHYVSRAVGGTGLIIMEMTDVDPDGRITDYDLGIWSDEHIPALARIVEACHSYGAKVGIQIAHAGRKAEDAQLPVAPSAIPFSAEYKTPRELTTEEVKAMVQKFQAGVERAVQAGFDVIELHGAHGYLIHQFHSPLTNKRTDEYGKDLTLFGREVIQAAKKVMPEGMPLIMRISAQEYVEGGYGIRESLEIGRAYKEAGADIFHVSAGGEGAIAAEGKPGTHAAYQIPLARAFKQELNVPVIAVGRLDEAVLANAVIGNDEADLVAVGRGMLRNPYWTLEAGVQLGKDAGLPKQYELGFPRSRR
>NZ_LN831776.1|WP_020426535.1|5501931_5502702_-|ABC-transporter-ATP-binding-protein
MPILDVHNLSKIYEGKVSIHALNHIRFAVEQGEFVGIMGPSGSGKTTLLNVIATIDEPTSGEVMINGRDPRGLGRKDRALFRRKELGFVFQHFNLLDTLTVEENVVLPLTLAGFTVQEMEYRLGEVADRLGIRALLDKRTNEISGGQMQRVAIARAMIHRPSLILADEPTGSLDSKAAGEVMNLLAEVNGTEGTTVLMVTHDAVAASFCHRVIFIKDGRFHSEMYRGSSRAAFFQNIIDMLSLLGGGGHDLPAVRL
>NZ_LN831776.1|WP_020426534.1|5500007_5501957_-|FtsX-like-permease-family-protein
MTFRQFAYRNVARNKRKYAAYFVSSAFSVMVFFLCALFIYHPAISRDMILGTAADTMMAAEGIIYVFCSLFVLVSVGSFLQSRKLEFGILLMHGMTKRQLKLMVFLENMMIGGSAILTGTLLGLLLGKLFLMIGSGFLGIEPLEFHLSWQAPVLTICSFVLLFMLISLLTFAFIGNESPRGLFRGGGRGEAEPEVSGGLALLAGLLLLAGYGLAAVTTAATIEIMMFPVVLITICGTYLFYTQLSLYIVGMLRKLRRFYWKHTHILTFAGLSYRWKDNGRMFFMVTIVSAVSFTSVGVFASIHTLSRELKLDYPAAVGYVAKGGGYASSEKRDLQGITAALERLGLPYETLRIPLKYAAIVSQTGPDHTKQLPLMSYSNYKLALRHAGFSSDEPPLAGNQGLVMIGSQRDRSLTAARFKATYTLKQGTRIQEIGYTQHVPIAEYLLPELDGRGGGDFSGLVVSDSLYSGIVPVHQDWYTGFYMEDFPRTAGIAPELAATGKVPYEAKSSYAVVISGTLFEIQRTLYSTMLFASLLVGTVFFIAAGSFLYFRLYVDLDHDRLQYSTLSKMGLTDRELDRIATLQLALMFFVPVLLAVLHSLFAFIALQRMFYLSIAAETGAVLTGYLAAQTLYFFFIRSRYLRNLKKNLI
>NZ_LN831776.1|WP_020426533.1|5499369_5499993_-|DedA-family-protein
MKTWITDIMEQFGYAGIFLMLALENIFPPIPSEVILPFGGFMTTTSGLTIPGVLIASTAGSLLGAAILYWIGRLLEVSRMERIVDRYGKWIRIKKSDIRKADAWFDKYGYWTVLFCRMVPLVRSLISIPAGMSGMKFGLFMLFTTIGTLGWNTLLILLGAALGESWEDIGGYIGTYSSIVYILLAGGILVLGLLYLRKRHTEGKARG
>NZ_LN831776.1|WP_020426532.1|5498417_5499287_-|undecaprenyl-diphosphate-phosphatase
MELLTIIKAIILGIVEGLTEFAPVSSTGHMIIVDDMWLKSQEFLGKYAANTFKVVIQLGSILAVVVIFRNRFIDLLGLKRFSRKELTAVPEGQPAVETTGRLKLAQVIVGLIPAGVLGFLFEDYIDEHLFSTSTVLIGLVVGAILMICADLLAPKKIKTESVDQITYRQALSVGLIQCLSLWPGFSRSGSTISGGVLLGMSHRAAADFTFIMAVPIMAGASLISLLKNWQYFTLDDLPFFIAGFISAFLFALLSMRFFLKLINRIKLMPFAIYRIILAAVVYFVWFYIS
>NZ_LN831776.1|WP_046504936.1|5508132_5508834_+|hypothetical-protein
MNLRQLQVEEGELICPQSPTSGQIKGIYTSPFTPLPTSGLIKGIYTFHFIQLPTFGLIKGIYTFHFTQPPTSGLIKGIYTSHSTQLPTSGQIKGIYTFHFTQLPTSALTKGIYTSHSTQLPTSGLIKGIYTSPFTRTLTSALTKGIYTSHSTQPPTSGPIKGIYTSHSTQLPTSGLIKGIYTSHSTQLPTSGLIKGIYTSPFTRTPTSGLIKGIYTSPSTSILESAFFRLTRS
>NZ_LN831776.1|WP_020431613.1|5509004_5509391_+|MerR-family-transcriptional-regulator
MDRMRIGELTERAGVTQRTVRYYESIGLLPSGEREGNGHHYYTEETVARLRKIDQLKKLGLSLEEIGDVIELYFTDPSGVQPKRKVLGLLRRHLADTDKKLDALGQFRDDLQSHIERFEQWLETNDRA
>NZ_LN831776.1|WP_020431612.1|5509457_5510282_+|NAD(P)-dependent-oxidoreductase
MSENIGFIGLGLLGLPIAANLLQARYALTVYNRTADKAKPLVAQGALQAARPADAVTTGGIVVTLVWDDEALESVVGSEDFLERLGPGGIHVSMSTVSPDTGRKLADLHARHGSVYVEAPVFGRPEAAAAKQLWIPVAGPQEAKERVRPVLEAMGARGIFDFGEEAGAAVLVKLIGNFLIVSAGRSLEEALGMAERGGLDPKAVVNMLTSTLFPAPIYQSYGKMIAEKTANISESKIPQKDVGLFLAAAQNAQFPAPLAGQLLDMLESGNRSRP
>NZ_LN831776.1|WP_020431611.1|5510644_5511436_-|TIGR00266-family-protein
MSAHEIDYVIMGEEIQCVEVQLDPGESVIAEAGSFMMMDPEISMETIFGDGTGSRGGGLMGKLMGAGKRLLTGESLFMTVFTHSGAYGRKSVTFAAPYPGKIIPLDLQQHGGKIICQKDSFLCAAKGVSIGIEFQRKLGAGFFGGEGFIMQKLEGDGLSFVHSGGYIMERTLQPGETIKLDTGCLVAMTSSVDYNIEFVKGVKTALFGGEGLFFATLRGPGKVWVQSLPFSRMADRILSAAGNSGRKEEGSILGGLGNLLDGR
>NZ_LN831776.1|WP_039790603.1|5511666_5512338_-|membrane-protein
MRKQDSGMGMPLRLTIILSGTLLLAFTYYHINYQNHLTEGGFVGLSLLGKYVLGISPSLTILILDIPVLLIAMIFKGRAFVLNTFISVGAFTVFYSLMERYSGWVINLQDNLPLAALLSGVLTGLGAGMVLRGGGASGGDDILSLLISEWKGIKVGTVFILMDVIVLALSLFYMPLKETLYTVMAVVVAGYVITFTTSLGRPKLGKAPTIQPTLSKPHDGTVM
>NZ_LN831776.1|WP_020431600.1|5512689_5513190_-|Crp/Fnr-family-transcriptional-regulator
MILHKGEVLFRQGDACQNLFQVKSGLFKVIRLHENGNMVLFNLLYPGETVPHHSLISPKEAHGTAVAMMKSEVELVPAAEWYRELREDPDKVMEIALLLQEKVRFMQTRLDHLTVGTPGERLDLLKRWLLEYSHGAELTDLLTQEEIGQLIGVRRETVNRLLRNPG
>NZ_LN831776.1|WP_020431599.1|5513390_5513924_-|adenylyl-sulfate-kinase
MSVNRGITLWLTGLSGAGKSTVAALVTDRLRAAGQAVEWLDGDELRRSIGRGLGFSREDRFENIRRAVYVAELLNRHGVITVISLISPYAEMRSHARQQLPGFVEVYVNCPLEICEARDVKGLYAKARRGELPSFTGISDPYEAPASPELTLYTAKHPPEDCADELLAWLEKRQQQG
>NZ_LN831776.1|WP_020431598.1|5513920_5514793_-|radical-SAM-protein
MRAVLYYRGALTSCNYDCPYCPFGKTRDSAERLAKDREELEAFVRWASAQGAEGHCLSIFFNPYGEALIHRWYKEAMITLSNLDHIDKVAIQTNLSAGLDFAARLNPHKAAFWATYHPGQVTEQRFLAQCMAVYEQGIPLSVGSVGIRSSFEAIASLRAALPEEVYLWVNAYKDKPNYYTGEDIAFLSGIDPYFMLNARDYESLGKACGAGSSVFYVQGPGQVKRCYKDRGVIGNLYRDGLEGLSAERSCRMKVCDCYIGYIHMPELQLQQVYGAGLLERIPCGVREGKE
>NZ_LN831776.1|WP_020431597.1|5514789_5516175_-|STM4012-family-radical-SAM-protein
MTSTQPPLHLRDDGRTPFPSEDVTQWREHITADPYRNYLYSYPHKTAYRDLNPPVPLEPLWREEPAESFFLYMHIPFCGARCGFCNLFTLPDKRAEVHTVYVDALERQARQWAAFTGGKPFARFAIGGGTPSLLAPAQLRRLFRIAEDIMGLDPASASISVETSPETLTEDKLNILKEHTVDRVSMGIQSFVAAESAAIYRPQNPDEVYRALELLKLYDFPVLNLDLIYGLPGQTVDSWLYSLEQAVNHEPEEIFIYPLYTRDHTIVKPEDIRRQTDIRHECYRAAQQLLAEHGYTQYSMRRFARATAGTHKSIIDYSCQEEGMVGLGCGARSYTRNVHYASRYGVSRKATESIIADYVAAERYDTADYGIVLSLEEQKRRYILKAVLHSEGLKLADYSGRFGSSLWRDHPELGLLLQSGLGREEEGRLRLTPEGLGYSDSIGDWFISGEIREQMERFVLP
>NZ_LN831776.1|WP_020431596.1|5516211_5516997_-|STM4013/SEN3800-family-hydrolase
MTDMNAVVGSHDLLMITLDTLRYDAAVLEEANCPNLCGTGSWEKRHTPGSFTYAAHHAFFGGFLPTPATTDKSRHVRLFHSRNTGMKTHPDTWLFDTPDVVSGLAAAGYRTLCIGGVIFFSKKVPLARVLPGYFQHSYWRMTFGVTNPRSTEHQVNHALKLLKDTPLDQRLFLFLNVSAIHGPNHYFVPGARKDSIDTQRAALRYVDGELGRLFGAFRERGNPVFCLAFSDHGEAFGEDGYHGHRLAHETVWNVPYREFFL

Crispr_ID: NZ_LN831776_58

• CRISPR_ID: NZ_LN831776_58
• CRISPR_location: 5533276-5533350
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_58

Consensus_repeat	Method
AAGTGGAAAAAGGGACACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_58

>58.1|5533299|29|NZ_LN831776|CRISPRCasFinder
TGCTGGAGTACCCTATCCTCGGGCAGATG

CRISPR arrays and Neighbor proteins around NZ_LN831776_58

CRISPR arrays

The CRISPR arrays of NZ_LN831776_58

>merge|NZ_LN831776|58|5533276-5533350|CRISPRCasFinder
AAGTGGAAAAAGGGACACTAATTTGCTGGAGTACCCTATCCTCGGGCAGATGAAGTGGAAAAAGGGACACTAATT

>NZ_LN831776|58|58|5533276-5533350|CRISPRCasFinder
AAGTGGAAAAAGGGACACTAATT	TGCTGGAGTACCCTATCCTCGGGCAGATG
AAGTGGAAAAAGGGACACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020431582.1|5525405_5526506_+|AI-2E-family-transporter	unknown	unknown	gnl|CDD|223701
NZ_LN831776.1|WP_020427217.1|5529887_5530550_-|hypothetical-protein	unknown	unknown	gnl|CDD|260015
NZ_LN831776.1|WP_020427216.1|5529139_5529808_-|uracil-DNA-glycosylase	unknown	unknown	gnl|CDD|235376
NZ_LN831776.1|WP_039788675.1|5537825_5538824_+|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_LN831776.1|WP_141639180.1|5524557_5524749_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046507329.1|5530703_5531279_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_LN831776.1|WP_020428979.1|5533934_5535062_-|hypothetical-protein	unknown	unknown	gnl|CDD|226785
NZ_LN831776.1|WP_020427215.1|5528703_5529108_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_141639115.1|5535182_5535581_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427220.1|5532191_5533094_+|hypothetical-protein	unknown	unknown	gnl|CDD|226076
NZ_LN831776.1|WP_020431584.1|5524767_5525241_-|hypothetical-protein	unknown	unknown	gnl|CDD|378584
NZ_LN831776.1|WP_020428997.1|5543370_5544099_+|rhamnogalacturonan-acetylesterase	unknown	unknown	gnl|CDD|238859
NZ_LN831776.1|WP_020427219.1|5531355_5531919_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020428993.1|5540353_5541841_+|altronate-dehydratase	unknown	unknown	gnl|CDD|377287
NZ_LN831776.1|WP_020428986.1|5536634_5536853_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020428995.1|5541874_5543299_+|glucuronate-isomerase	unknown	unknown	gnl|CDD|376859
NZ_LN831776.1|WP_020428988.1|5537056_5537266_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020428984.1|5535731_5536406_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046503097.1|5528172_5528370_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020428992.1|5538905_5540327_+|tagaturonate-reductase	unknown	unknown	gnl|CDD|235147

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020431582.1|5525405_5526506_+|AI-2E-family-transporter	gnl|CDD|223701	COG0628, yhhT, Predicted permease, member of the PurR regulon [General function prediction only].	1.21586e-51
NZ_LN831776.1|WP_020427217.1|5529887_5530550_-|hypothetical-protein	gnl|CDD|260015	cd13935, RNase_H_bacteria_like, RNase H is an endonuclease that cleaves the RNA strand of an RNA/DNA hybrid in a sequence non-specific manner. This family includes bacterial ribonuclease H (RNase H) enzymes. RNases are divided into two major families, Type 1 and Type 2, based on amino acid sequence similarities and biochemical properties. RNase H is an endonuclease that cleaves the RNA strand of an RNA/DNA hybrid in a sequence non-specific manner in the presence of divalent cations. RNase H is widely present in various organisms, including bacteria, archaea and eukaryotes. Most prokaryotic and eukaryotic genomes contain multiple RNase H genes. Despite the lack of amino acid sequence homology, type 1 and type 2 RNase H share a main-chain fold and steric configurations of the four acidic active-site residues and have the same catalytic mechanism and functions in cells. RNase H is involved in DNA replication, repair and transcription. One of the important functions of RNase H is to remove Okazaki fragments during DNA replication. RNase H inhibitors have been explored as an anti-HIV drug target because RNase H inactivation inhibits reverse transcription.	9.47468e-65
NZ_LN831776.1|WP_020427216.1|5529139_5529808_-|uracil-DNA-glycosylase	gnl|CDD|235376	PRK05254, PRK05254, uracil-DNA glycosylase; Provisional.	1.9234e-145
NZ_LN831776.1|WP_039788675.1|5537825_5538824_+|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	9.28085e-106
NZ_LN831776.1|WP_046507329.1|5530703_5531279_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	2.09406e-08
NZ_LN831776.1|WP_020428979.1|5533934_5535062_-|hypothetical-protein	gnl|CDD|226785	COG4335, COG4335, DNA alkylation repair enzyme [DNA replication, recombination, and repair].	4.84619e-60
NZ_LN831776.1|WP_020427220.1|5532191_5533094_+|hypothetical-protein	gnl|CDD|226076	COG3546, COG3546, Mn-containing catalase [Inorganic ion transport and metabolism].	5.84456e-93
NZ_LN831776.1|WP_020431584.1|5524767_5525241_-|hypothetical-protein	gnl|CDD|378584	pfam11181, YflT, Heat induced stress protein YflT. YflT is a heat induced protein.	0.000181202
NZ_LN831776.1|WP_020428993.1|5540353_5541841_+|altronate-dehydratase	gnl|CDD|377287	pfam04295, GD_AH_C, D-galactarate dehydratase / Altronate hydrolase, C-terminus. Family members include the C termini of D-galactarate dehydratase (EC:4.2.1.42) which is thought to catalyze the reaction D-galactarate = 5-keto-4-deoxy-D-glucarate + H2O, and altronate hydrolase (altronic acid hydratase, EC:4.2.1.7), which catalyzes D-altronate = 2-keto-2-deoxygluconate + H2O. As purified, both enzymes are catalytically inactive in the absence of added Fe2+, Mn2+, and beta-mercaptoethanol. Synergistic activation of altronate hydrolase activity is seen in the presence of both iron and manganese ions, suggesting that the enzyme may have two ion binding sites. Mn2+ appears to be part of the enzyme active centre, but the function of the single bound Fe2+ ion is unknown. The hydratase has no Fe-S core.	0
NZ_LN831776.1|WP_020428995.1|5541874_5543299_+|glucuronate-isomerase	gnl|CDD|376859	pfam02614, UxaC, Glucuronate isomerase. This is a family of Glucuronate isomerases also known as D-glucuronate isomerase, uronic isomerase, uronate isomerase, or uronic acid isomerase, EC:5.3.1.12. This enzyme catalyzes the reactions: D-glucuronate <=> D-fructuronate and D-galacturonate <=> D-tagaturonate. It is not however clear where the experimental evidence for this functional assignment came from and thus this family has no literature reference.	0
NZ_LN831776.1|WP_020428997.1|5543370_5544099_+|rhamnogalacturonan-acetylesterase	gnl|CDD|238859	cd01821, Rhamnogalacturan_acetylesterase_like, Rhamnogalacturan_acetylesterase_like subgroup of SGNH-hydrolases. Rhamnogalacturan acetylesterase removes acetyl esters from rhamnogalacturonan substrates, and renders them susceptible to degradation by rhamnogalacturonases. Rhamnogalacturonans are highly branched regions in pectic polysaccharides, consisting of repeating -(1,2)-L-Rha-(1,4)-D-GalUA disaccharide units, with many rhamnose residues substituted by neutral oligosaccharides such as arabinans, galactans and arabinogalactans. Extracellular enzymes participating in the degradation of plant cell wall polymers, such as Rhamnogalacturonan acetylesterase, would typically be found in saprophytic and plant pathogenic fungi and bacteria.	2.07278e-81
NZ_LN831776.1|WP_020428992.1|5538905_5540327_+|tagaturonate-reductase	gnl|CDD|235147	PRK03643, PRK03643, tagaturonate reductase.	0

Protein sequences

>NZ_LN831776.1|WP_020427220.1|5532191_5533094_+|hypothetical-protein
MFQRMDEIMIEIPDVEKPDPNAAAAVQELLGGKFGEMSTLNNYLYQSFNFRSKDKLKPFYDLVMSITAEELGHVELVSHAVNKCLRGSTAYKQPDSTPLHAVKDARLSYHFLAGAQGAMPFDSMGNPWTGANVFNSGNLVEDLLHNFFLECGARTHKMKVYEMTDHPAARAVVGFLLVRGGVHVVAYAKALEIATGVNVTKLVPVPSLSNKSFTEAAKYEEKGVHTKLYTWSNKDFSSIGQIWKGTHPEDGLPLEVIQGVPEGVPIPEAPESKEEFAPGISAEEFKEIAKRLKMAGNIHD
>NZ_LN831776.1|WP_020427219.1|5531355_5531919_+|hypothetical-protein
MKKLAALAAIFVLTLLVGCGSSANNNNTAGTNTPANNGNTSTATAAPDAVTSASVVDNGEDFKKAISKEGTWIAATLKDLSFTEDLVVEGEFSNKGKPARKIALYTQDADHNITNSFRLAAPKITIKSENTQIQGGTFVGDVYVEANGFKVVNATIEGNVYFSDDKYQATYSAADQGKVTGVTEVKK
>NZ_LN831776.1|WP_046507329.1|5530703_5531279_-|TetR/AcrR-family-transcriptional-regulator
MARSKEFDVDNVLGKAMNVFWQQGYEKTSMQDLVAGMGIHKRSMYDTFGDKHSLYIKSMERFADMTASRMEGRVEGVDSAKEAIRRLFDMIIYKQEMDPAGCLLVNSAVELANHDPETTSRVNDAFLNAERLLEQLITRGQASGEIAEHHRAADLAVFLHNALVGLRVMVKINPDPSKLQRIADTTLAVLD
>NZ_LN831776.1|WP_020427217.1|5529887_5530550_-|hypothetical-protein
MAKQKYYVVWEGKKPGVYGTWAECQAQTDHYTGAKYKSYESRAAADAAYKAGWKGNWGSGAAAAGAGKSKPASSYKRSTAEAAPAEIEYDSISVDVGTRGNPGPVEYKGVDTQTGDIIFSCGPISKGTNNLGEFLAIVHALALLKKEGSSRTIYSDSVNAMKWVKQKKVATTLPRDASTEEIWTLIDRAERWLQTNTYTNKILKWQTREWGEIKADYGRK
>NZ_LN831776.1|WP_020427216.1|5529139_5529808_-|uracil-DNA-glycosylase
MFGNDWDDILQEETQKPYFQELRYALAREYKQYTVYPPKEELFSALKLTPYNSTRVVILGQDPYHGAGQAHGLSFSVKPGVRVPPSLRNIYTELHDDMGVSIPNHGSLLHWAEEGVLLLNAVLTVREGQPNSHKGLGWETFTDAVMEKLNERKAPLVFILWGSHAQQKGAYIDRSRHLVIQSPHPSPFSAHRGFLGSRPFSRANQYLESHGLQGIDWSIPNI
>NZ_LN831776.1|WP_020427215.1|5528703_5529108_-|hypothetical-protein
MKHWVGRPVIMYCGEEPYTIMKGVLRKWDPAASVAVIGHQEITVPFRDIVFIKALAPKERALAPTLHAVGYVMRERQQFDNAIYFKSAVTVWKGDQLIAYNTTITSHTKGSVTLKDGQNLLKGSHVFVVRSLRG
>NZ_LN831776.1|WP_046503097.1|5528172_5528370_-|hypothetical-protein
MEKGNLFFRKLRNPEIEVEKVNLITHGLAATVGHENQVKSEYIFGKIVLWIRGRFNIGETSRNLI
>NZ_LN831776.1|WP_020431582.1|5525405_5526506_+|AI-2E-family-transporter
MLQSKYFRTCLAIIAFLTILYLGSKVVFLITPLVAIFNLLLVPMMLSGFMYYLLRPLVNFLESKKLNRMLSILLIYVVFIGLFVLFWVLVWPTLREQIQNFIDNTPYLVQGIQEQFNKLQSDPYFSRFFKGDADLTARISGYLSDTITWVTNSMSNLISVVSSIVVVIATLPIILYYMLKDGHKLSPILLSLVPRKYRKEGQDMLQDIDSALSGFIVTRVLLNVVLGAMLYVGFLIIGLPYSLMLAIISIPLNFIPYVGSLLAAVPVVIVGFIESPTMAIWSVVVIIIAQQIQDNVLSPIIYGKSLDVHPLTTVVLVLVGGDFYGIIGVLIALPVYMILKIIFLRIYEIIIAERVEEVTVVKEEQL
>NZ_LN831776.1|WP_020431584.1|5524767_5525241_-|hypothetical-protein
MTILVVGIFEHPSDAALAIEAVREQGVKPKQISVVTKQKNTLKRISHDTGIGRTESGEGNEGLFGTAKALGVGLEMLPDTAVAAGPAARKLAGADLEGDGLAVSLISIGIPQEDAEIYARHAGKEHIIVIVTLEEKQNQQAVSTLFEQHHAIPPGSP
>NZ_LN831776.1|WP_141639180.1|5524557_5524749_+|hypothetical-protein
MDAEDYAIIAAGLTALGDIFAFLSLVKAKQVTKETGGQAGIDPLLFIRSKKNKAAKRKNRPLL
>NZ_LN831776.1|WP_020428979.1|5533934_5535062_-|hypothetical-protein
MAEPLKAMYNEGFLRSFGTKLQSVYSGFDLEGFVTAAMKDPWEELELKGRMRRITETLGTFLPRRYEDALEILFAIDKECVGFPYLIFPDFVEVFGGSEEHWELSMSALERFTPKSSAEFAVRPFLLRDPQRMMAQMLRWSQHPDEHVRRLSSEGSRPRLPWGQALPMFKHDPSPVLPVLEQLKADSSLYVRKSVANNLNDIAKDHPGVVIDIVRRWKGVNAHTDWIVRHGCRTLIRKANPEIMALFGYAGQEDESPLAVSAVLSVEPAELPIGGSCELAYALAVREGDEARIRIEYGIDFVKAGGKTSRKLFLLSDKTVPGGTRLSGKRTHRWVDLTTRRHYAGEHKITLLVNGREAASAVLVLKPQRKGDLEL
>NZ_LN831776.1|WP_141639115.1|5535182_5535581_-|hypothetical-protein
MPDEPLEEYGIQRCSKLFIMSGSGTSGGFSVMSRGMLEVHKSYLLDVLKKDPVLFNQTEEGYIYRTKQRIFSWVYLDERNVISFPENVMEAMGISIQDELLSIRSSNVAFVNILQGPIVDRARKSTELKHYS
>NZ_LN831776.1|WP_020428984.1|5535731_5536406_-|hypothetical-protein
MRLLVSQPNHESGLLRMQQELKQWSEYCDAVLYPEGYVADTGSVQTLRSLAGQYRKLMITSYKNDNGQDRALVIGPDGEIVLERPKSPMQGELYAPSVVAAGAIRMGYLLCVEILQGLNGLEGHAGTLDFIAHPIGVGMFSEEQFALWTEEAARIAVKYQCPIIGTSHADGSYRNCGVSIPISYCITANGQPLYISHADTRSRIVDLKSGTVAIAGTDYKPAMR
>NZ_LN831776.1|WP_020428986.1|5536634_5536853_+|hypothetical-protein
MPQTLVKNVDFFVAALSQTYVSALQLDPDGMYSQVGIGIVEKFAEDYVRLKRFDGSVSHYDREITKFQHNKA
>NZ_LN831776.1|WP_020428988.1|5537056_5537266_+|hypothetical-protein
MSDKADFRDERTPGFSQIPDASIRPGQTASTDKLDDIVGGIMDNVQETLTGDSPENSGKNPAGEKTGDK
>NZ_LN831776.1|WP_039788675.1|5537825_5538824_+|LacI-family-DNA-binding-transcriptional-regulator
MMITIKDIARVAGVSHTTVSRALNGSPLIKKVTRDKIEKIAAEMNYVPNYSAKSLVTKRSFTIGLFFSSIEQGTSASFLVDAIKGISHILDENFNLTVNGIDGVHNFGNIQPQRFDGILVMSQSDEDNAFIYHVKKMGIPLVVLNRQLEDPGIMNVVANDREGVKEAIDYAVRQGHRKLAIIEGKPGFKSSSERKQGFMDSLIAHRLPLNSGYFAAGDYSIESGYAAMAALLQLEDPPTAVFCSNDDMAIGAMNACYAHKADVPGQISLLGFDDIMFSRYTNPALTTVRKPITEISELGTKMLVQLLQQPETQPQQLFVNTSLVIRQTVAEV
>NZ_LN831776.1|WP_020428992.1|5538905_5540327_+|tagaturonate-reductase
MTQRLSRTTQPGLPQYPERMIQFGEGNFMRAFVDWQLQQMNQQGLFNGSAAVVVPIGQGIGGLMAEQDNLYTVLLNGIMQEQPVNSREIITSVSRVINPYSDYEAYLALAENDELEFITSNTTEAGIAYQPEDRLEDAPPSSFPAKLTALLYRRFELGKKGFVIIPCELIDRNGEKLKEIVRQYAAAWNLGEAFLQWLDDENTFCCSLVDRIVPGYPRGKAAELEAELGYLDKLMVTAEPFLFWVIEGPAWLSERLPLAKAGLNVVVTDDMTLYRERKVHLLNGPHTAMVPLAMMAGLETVEDVMNDETFYRFVRRLLDEELIPVLDLPQEELLSYADAVLERFKNPFIRHELASISLNSISKFKTRLLPVLLRYQQERGQLPPLITLAFAGLLLSYRGDRVKRQDSAEVLAVFDQAWSQPSTFTASILREVSLWGQDLTQVPGLTEAVDARLHQLQSSDSRAALQQLVRSEV
>NZ_LN831776.1|WP_020428993.1|5540353_5541841_+|altronate-dehydratase
MKRLMKMNPRDTVAVALRPIASGEVLSFEGLSLTAAQDIPQGHKIALTSFAEGDVITKYGYPIGHAVEEIRAGDWIHTHNIKTNLSGEEEYEYLPDLHPVTYPKRGLTFQGYRRANGKVGIRNDLFIIPTVGCVNGIAEQMLQEFKAEHPDLGGFDNFTVLKHPYGCSQLGDDHRMTRSILLDAVNHPNAGGVLVFGLGCENNIVSEFRSMLGDYDGSRVKFLVAQEVGDEVEAGLALLEELYEAAKNDVREPVPLSELNIGLKCGGSDGFSGITANPLLGAFSDFIISQGGTSVLTEVPEMFGAEKMLMARAENREVFEDIVSLINNFKQYFLSYGEPVYENPSPGNKAGGISTLEDKSLGCTQKAGSSPVVDVLDYGVKLRRKGLSLLQAPGNDLVAASALAASDCQLVLFTTGRGTPFGSFVPTVKVATNNDLFAKKGHWMDFNAGPLLERPMADVLEEFIAYIIDVASGQKTRNEQNEVRELAIFKTGVTL
>NZ_LN831776.1|WP_020428995.1|5541874_5543299_+|glucuronate-isomerase
MFLNDDFLLTSETARLLFHNHAKTMPIIDYHCHLDPKEIYEDKAFRNLTEAWLAGDHYKWRLMRANGIPESHITGEASDYDKFLAWARTLPKAVGNPLYSWTHLELRRFFGINETLNEASAPAIWEEVNRKLAEPAYTRRSLIRNSKVKTVCTTDDPADSLEYHRLLKESEQDFQVFPTFRPDKALNIDADGFTTWLTRLGEAAGVAVTTYAALVEALRSRVDFFHQNGCRLSDHALDVLRYQAAGEASQLERIFTKRLEGAVLSPEEITVYRTELLSELIGMYHDKNWTMQLHLHAFRNNNTPMFRRLGPDTGYDGINDLSLAEALSQLLDRAECGKGLPKTILYSLNPGDYPALLALMGCYQKDTAGKLQLGSGWWYNDTRDGMRRQLTLLADNSLLGNFVGMLTDSRSFLSYTRHEYFRRVLCELLGELADRGEAPDDLALLGQLVEDIAYNNAAGYFGFEARSAAKLQHR
>NZ_LN831776.1|WP_020428997.1|5543370_5544099_+|rhamnogalacturonan-acetylesterase
MPTLYIAGDSTAAQKGGGEKPMAGWGEFLQEHFSPEIAVDNRAVNGRSTRSFLAEGRLEDIGKDFQCGDYLLIQFGHNDQKVEDPARYTDPAAEYRRNLLTFIEFARSRGGSPVLLTSVSRRRFTAGGEPDPLAVGLYPEAVREVAAQTGTPLLDIFASSQQLYRGLGVDGSRQLFMHLPAGGHPNYPQGITDDTHFCKQGAARIADLVAEAISQSAELAALHAHLRQPGSWSPRIYLGFPV

Crispr_ID: NZ_LN831776_59

• CRISPR_ID: NZ_LN831776_59
• CRISPR_location: 5654475-5654549
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_59

Consensus_repeat	Method
CCAACAACGGTATTTCTGCCGTTG	CRISPRCasFinder

spacers of NZ_LN831776_59

>59.1|5654499|27|NZ_LN831776|CRISPRCasFinder
TTTTCGGGCAAGCTGGCCTTCGACGAC

CRISPR arrays and Neighbor proteins around NZ_LN831776_59

CRISPR arrays

The CRISPR arrays of NZ_LN831776_59

>merge|NZ_LN831776|59|5654475-5654549|CRISPRCasFinder
CCAACAACGGTATTTCTGCCGTTGTTTTCGGGCAAGCTGGCCTTCGACGACCCAACAACGGTATTTCTGCCGTTG

>NZ_LN831776|59|59|5654475-5654549|CRISPRCasFinder
CCAACAACGGTATTTCTGCCGTTG	TTTTCGGGCAAGCTGGCCTTCGACGAC
CCAACAACGGTATTTCTGCCGTTG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_046505009.1|5657906_5658620_-|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225099
NZ_LN831776.1|WP_020431094.1|5661066_5662437_-|HAMP-domain-containing-sensor-histidine-kinase	unknown	unknown	gnl|CDD|274368
NZ_LN831776.1|WP_020426109.1|5652237_5653197_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_063850482.1|5640895_5646115_-|hypothetical-protein	unknown	unknown	gnl|CDD|377038
NZ_LN831776.1|WP_020426118.1|5635029_5635986_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_LN831776.1|WP_020431099.1|5658716_5659529_-|fructoselysine-6-kinase	unknown	unknown	gnl|CDD|238915
NZ_LN831776.1|WP_020427312.1|5664045_5665461_-|glucuronate-isomerase	unknown	unknown	gnl|CDD|376859
NZ_LN831776.1|WP_020431107.1|5656232_5657816_-|amidohydrolase-family-protein	unknown	unknown	gnl|CDD|238625
NZ_LN831776.1|WP_020426110.1|5651389_5652238_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_020431092.1|5662433_5663108_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_LN831776.1|WP_046505012.1|5659544_5660513_-|SIS-domain-containing-protein	unknown	unknown	gnl|CDD|225132
NZ_LN831776.1|WP_046505020.1|5665537_5667148_-|mannitol-dehydrogenase-family-protein	unknown	unknown	gnl|CDD|223324
NZ_LN831776.1|WP_020426111.1|5649533_5651291_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_020426113.1|5646788_5648147_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_LN831776.1|WP_020426112.1|5648260_5649559_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|227095
NZ_LN831776.1|WP_046505001.1|5636974_5638726_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270300
NZ_LN831776.1|WP_020426117.1|5635996_5636899_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_039785486.1|5638799_5640860_-|hypothetical-protein	unknown	unknown	gnl|CDD|379757
NZ_LN831776.1|WP_020431109.1|5654799_5656230_-|putative-basic-amino-acid-antiporter-YfcC	unknown	unknown	gnl|CDD|224207
NZ_LN831776.1|WP_046505016.1|5663286_5663676_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_046505009.1|5657906_5658620_-|GntR-family-transcriptional-regulator	gnl|CDD|225099	COG2188, PhnF, Transcriptional regulators [Transcription].	8.67947e-71
NZ_LN831776.1|WP_020431094.1|5661066_5662437_-|HAMP-domain-containing-sensor-histidine-kinase	gnl|CDD|274368	TIGR02966, Phosphate_regulon_sensor_protein_PhoR, phosphate regulon sensor kinase PhoR. Members of this protein family are the regulatory histidine kinase PhoR associated with the phosphate ABC transporter in most Proteobacteria. Related proteins from Gram-positive organisms are not included in this model. The phoR gene usually is adjacent to the response regulator phoB gene (TIGR02154). [Signal transduction, Two-component systems].	3.02206e-67
NZ_LN831776.1|WP_020426109.1|5652237_5653197_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	3.07158e-78
NZ_LN831776.1|WP_063850482.1|5640895_5646115_-|hypothetical-protein	gnl|CDD|377038	pfam03442, CBM_X2, Carbohydrate binding domain X2. This domain binds to cellulose and to bacterial cell walls. It is found in glycosyl hydrolases and in scaffolding proteins of cellulosomes (multiprotein glycosyl hydrolase complexes). In the cellulosome it may aid cellulose degradation by anchoring the cellulosome to the bacterial cell wall and by binding it to its substrate. This domain has an Ig-like fold.	3.38766e-17
NZ_LN831776.1|WP_020426118.1|5635029_5635986_+|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	7.45804e-128
NZ_LN831776.1|WP_020431099.1|5658716_5659529_-|fructoselysine-6-kinase	gnl|CDD|238915	cd01940, Fructoselysine_kinase_like, Fructoselysine kinase-like. Fructoselysine is a fructoseamine formed by glycation, a non-enzymatic reaction of glucose with a primary amine followed by an Amadori rearrangement, resulting in a protein that is modified at the amino terminus and at the lysine side chains. Fructoseamines are typically metabolized by fructoseamine-3-kinase, especially in higher eukaryotes. In E. coli, fructoselysine kinase has been shown in vitro to catalyze the phosphorylation of fructoselysine. It is proposed that fructoselysine is released from glycated proteins during human digestion and is partly metabolized by bacteria in the hind gut using a protein such as fructoselysine kinase. This family is found only in bacterial sequences, and its oligomeric state is currently unknown.	6.70763e-105
NZ_LN831776.1|WP_020431107.1|5656232_5657816_-|amidohydrolase-family-protein	gnl|CDD|238625	cd01300, YtcJ_like, YtcJ_like metal dependent amidohydrolases. YtcJ is a Bacillus subtilis ORF of unknown function. The Arabidopsis homolog LAF3 has been identified as a factor required for photochrome A signalling.	2.0225e-76
NZ_LN831776.1|WP_020426110.1|5651389_5652238_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	8.32418e-86
NZ_LN831776.1|WP_020431092.1|5662433_5663108_-|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	1.8754e-84
NZ_LN831776.1|WP_046505012.1|5659544_5660513_-|SIS-domain-containing-protein	gnl|CDD|225132	COG2222, AgaS, Predicted phosphosugar isomerases [Cell envelope biogenesis, outer membrane].	1.77977e-92
NZ_LN831776.1|WP_046505020.1|5665537_5667148_-|mannitol-dehydrogenase-family-protein	gnl|CDD|223324	COG0246, MtlD, Mannitol-1-phosphate/altronate dehydrogenases [Carbohydrate transport and metabolism].	2.54806e-108
NZ_LN831776.1|WP_020426111.1|5649533_5651291_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	3.59237e-54
NZ_LN831776.1|WP_020426113.1|5646788_5648147_-|extracellular-solute-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	9.0086e-44
NZ_LN831776.1|WP_020426112.1|5648260_5649559_-|response-regulator-transcription-factor	gnl|CDD|227095	COG4753, COG4753, Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain [Signal transduction mechanisms].	1.34582e-89
NZ_LN831776.1|WP_046505001.1|5636974_5638726_+|extracellular-solute-binding-protein	gnl|CDD|270300	cd13582, PBP2_AlgQ_like_3, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	0
NZ_LN831776.1|WP_020426117.1|5635996_5636899_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.81739e-57
NZ_LN831776.1|WP_039785486.1|5638799_5640860_-|hypothetical-protein	gnl|CDD|379757	pfam15979, Glyco_hydro_115, Glycosyl hydrolase family 115. Glyco_hydro_115 is a family of glycoside hydrolases likely to have the activity of xylan a-1,2-glucuronidase, EC:3.2.1.131, or a-(4-O-methyl)-glucuronidase EC:3.2.1.-.	1.44165e-65
NZ_LN831776.1|WP_020431109.1|5654799_5656230_-|putative-basic-amino-acid-antiporter-YfcC	gnl|CDD|224207	COG1288, COG1288, Predicted membrane protein [Function unknown].	4.99981e-155
NZ_LN831776.1|WP_020427312.1|5664045_5665461_-|glucuronate-isomerase	gnl|CDD|376859	pfam02614, UxaC, Glucuronate isomerase. This is a family of Glucuronate isomerases also known as D-glucuronate isomerase, uronic isomerase, uronate isomerase, or uronic acid isomerase, EC:5.3.1.12. This enzyme catalyzes the reactions: D-glucuronate <=> D-fructuronate and D-galacturonate <=> D-tagaturonate. It is not however clear where the experimental evidence for this functional assignment came from and thus this family has no literature reference.	0

Protein sequences

>NZ_LN831776.1|WP_020426109.1|5652237_5653197_-|sugar-ABC-transporter-permease
MNNAAVKQAPAGSLKTVPSSKKRAKRWESPLAGYLFLSPWLIGFFLLTLGPMIMSLYYSFTDYSLLTAPKWTGLANYTRIFTEDDIFPSSLRITITFVLLTVPLRLMFALGIAMLLNRKIKGISFYRTMVYFPSLIGTSIAVSILWKNIFSRNGFINDFLAIFGIKGPAWIADPKYALGTLILLMVWQFGSSMIIFLAGLKQIPGDLYEASSVDGAGKFRQFFSITLPMLSPIIMFNAIQTMINTFQMFTQAFVITGGGPVKSTFVYVMYLYEEAFTKFHMGYASALAWVLLLLIGLFTAVLFGTSKYWVFYESQGGKK
>NZ_LN831776.1|WP_020426110.1|5651389_5652238_-|carbohydrate-ABC-transporter-permease
MEATRSSKRFVTHISLLVVSLIMMYPIFWWLGASLKTNEEMSSANLFPKIPHWANFSDGWVSVPNFTFAHFYLNTFELVAGVLFTSVVACSLVAFAFSRLDFPLRNFWFAIMLVTLMLPTQVTIVPQYVMFSKWGWINTYLPFYIPHLFAGGIGGPFFIYLLVQFMRSVPKELDEAAKIDGCSWFSIYWRIMLPLVKPALVTVAIYCFLWNWDDFFGQMLYINTIDKYTINLALKLFIDSQGSVPWGQMLAMSLVSIVPSVLIFFLAQKHFVEGMSAGALKG
>NZ_LN831776.1|WP_020426111.1|5649533_5651291_-|sensor-histidine-kinase
MRVNPFKTLRIDVVFFFGFALIVAILVGLIVWFSYINGSKEIAGNTSYYQQKLLIELHKKLNTNLEDIEQSSNTAAQNFNDQYEEMLDGNAYDQVRGQASIRSQLNNYVFGMPILQSIHVYSDLTPSYNVQDFVQFLPIGQMEREAWYDDLRNSDYAWLSERTIKTNSGDTSVISFARKVYNRFNRAFAVMVFNVRVPAFQSLIATEDSRSNLALLDATDKLITSTGDEAFFQQHEAQIKAQLDSRTNGAKRTGDEFLVWSSSLDSQWSLVEITSWSQITAGSLKQTKVILALGIATIVMILLLAVFLSRQFVKPIGLVLKAMSNFSLSKRTPLPDDYKNEFGRLFQGYEKLTYRIEELYDSLEQQHEQQRAAEIKALQMMINPHFLYNSLDQVNWMAIEASQPQISSMLSHLGQFFRLALSNSDSLVPLSEELAHIESYLQFQKIRWEDRLEYRFIAADEVKSLFVPKIILQPFVENAFIHGFHGKRQASLIITVSILEGQMLQITVMDNGRQLQENWMEKRSAKGGYGLRNVRERITAMFGSTYGFTLGNSPEGGTQAVICLPVLYSPSVKGGTQHVESSHHR
>NZ_LN831776.1|WP_020426112.1|5648260_5649559_-|response-regulator-transcription-factor
MWKVVIIDDDFQVVRGLRKAIPWEELDAEFAGEAIDGESGLKLIGEVNPDIVLTDIYMPVMNGIQMIEQLKAGSFAGRFVILSGYNDFEYARTALRLGVDDYLTKPVTVDQIRKVLSETIEKLEETYLHRLELGGGQSSDRQEAPSLAEWLVAVLNGWSQNPGLPAPLQQLDKQRYTVMVMEVLWTERIRSVSLADWNLFQFAVSNIVTEVYGREWPEAFFVWLFGNHAALLLPSAAQGPEGQIIQAADALGALIVSSIKTFLGLEVRFGIGNVKDGWDEIKASGDEAMQRLFAKLPLNLNHEKVWSGGAETQIDGLRKAQGPTIHDKHRKAVQFMIEYIHTHYAEDITLEHLASQLYISKNYLNQLFKKVTGETFTNYVIRVRIEKAKTLLQGGSHLIYEVSEMVGYQNVPYFSTLFKKYCGVSPSELMKR
>NZ_LN831776.1|WP_020426113.1|5646788_5648147_-|extracellular-solute-binding-protein
MHKMAKKSFLAIALMAMVATSAACGNNSNNGAAANNTEGGSTAATTAPAAGAGGTGSGSGEPVTLTVAWWGSQARHDATLKALDQYKALNPNVTFQTQFSGWDGYFDKLAVQYSAKSAPDIIQMDAAYLNDYAGRGLLADLKEVNVENIEATTMDGGKVNGTQYAVPLGVAALGMVYDKTVVEKLGLEAPKFGWTWDDYYAFGEAAKAKLGEDKYVFADQSADLVDYTAYQYSMGKGYIFDAEGNLSVDKDTWIGFMTKMDELRKKGILTPADITTTDKELDPQLDSVINGNAVVRHLFSNQVGSIEALKPDAFGYASMPYGTEAGGWLKPGMFWSVNAQSAHQAEAVKFVDWFVNNEEAGKTLGLTRGTPVNSKVVEALTPTFSDADKTSLDFLNQVTPDAQKFINDPQGWGNFKNDYKTIVEKLQFGQSTPEEAYAELLKTAEQYTAEAK
>NZ_LN831776.1|WP_063850482.1|5640895_5646115_-|hypothetical-protein
MKARRLGKGKTWLSILLIAVMLFAMVPGADQAEASSATGVTYYLDSAAGNDSNTGTTENRPWKSLSKVNSTVFQPGDRILLKSGGVWNNQTLAPQGSGSAGNPVIIDRYGSGDKPKIQAGGQFKDAVTLSNQQYWEIRNLDVSNTAPVTGTFAESLGDFRGIHVTGADAGTLAYFRISGVDVHDVSGEIAWISGTVPETPDPGIRFKTGWDGSKKTGGIVFDTTVADPLHPQRATVFNDVIIENSTVKNTSFGGIIFKQYAGDGGGDSSSGVVSTGWGTRDSETDAKFTPHTNIIIRGNYITQKATDFGCNAMYLTGVRGALVEHNVVDGAGTSGIEAYYADDVTIQFNEVFDTSKKAGGADSNGIDPDKGTTKILIQYNYVHDNGDGILICQFSFGDTIIRYNVLESNTRYPVYLHSDKKAVAEVYNNTIYNDASGYMIYGYGTSLNATYNIRNNILYTTRAVQELTLSPTIMYDNNSYYASAGALTPPAGDSHARTGNPQLADPGKGTSGTETDGPALDSLGGYQLKPESMLINRGLNILDPASAGVKDFAGQPLYNGNADLGAFEYYDPSLTTATLAGRITNSAGKGMSGVQVSDSSGSSLSAVTDSSGYYVIPGVAVGSSINLKAVKTGYADSETGMFAVAAGNVITRDLQLTSNAATGSVAGTILDGELTPAAGVTVTLTAEGAAVQTAVSDLNGGYNFPAVEIGENYTVSAAKSGYRAAEVSGIHVEPALLTKVADLYVVSKQAVLLNASDFNELAAGAQPSAPWTVTTTGGSVGAAELPGAADKSIKLTRSSNSGNTSMSQTFAPGTLKGVVTLSADVMKLDNAGSTNWISLPYIYSSAGTASTNVGVSLAFSKGQIVAYKGGTSTNLMPYETNKWYNLRLVMNTGSGKFDLYVDDVLVVDQAAFRNKIPDIGRIDYYANSSNYGTAYLDNVQLYQGIPYERNDAGLSGLTADLGPLTKQGEDYSLDVPYFMDSVQLTATASSPNIASLTINGIPAVSGQPAGEVALAEGLTTIPVVVTAEDGLTTHTVNVIINRTPAALDSTLQNLQVAASGGEELPLSPVFSYNRDSYTVNVADSVYGLTVTPVAGAPGTEIRVNGNVVGSTQTSAEIPLRASSSEITVTTASADGTDYRSYSITVNWEGTYPPGEEEVSDSSVSPTQAVFDKNTANSQAVALKVQANGNLLTAIRNGETPLGEADYTVTGNVYSIGVPYLLQQPLGMVSLVFDFNQGKDPIVDIQIIDTTDEGNGGGTGPGTGTDPGAGTDPGTGTNPGTDTDPGIGTDPGTGNNPGTGVNPGTGVNPGNGTYPGTGTGGNSSSGGGSGSSTAAVPAVTVSSGKLTVNPKYTAGSEAAQVAVTQEALNEALALAAAEGAGSKRVVIAVNQAAGATAYEVSLPAAALSAAATGQSLEIQTVVGAVVLPGGMLTAEQAAQNAAVVLRISAADAGSLPAEITAASAGRPVVKLSLSIGGKEISWQKSPAQVQVSIPYRLTAAELLNSDYLTVRYIDEAGVSHPVASGKYDPVSAAVTFTARHFSTYAVVMNRISFNDLDASHWAKKPVEVLAAKGIVNGVSAGSYAPAAQISRADYAVMLVRAFGLDGSAEAAATRFTDVLPGSYYYEAVNTAKALGIASGNTDGSFNPAGIITRQEMIVMTDRALTAAGVSSAATDGSGTGDAAAAAGFRDLAAVADYAAEAVNRMLQIGWLQGNSGLIQPEGTASRAEAAVLLYRICTEL
>NZ_LN831776.1|WP_039785486.1|5638799_5640860_-|hypothetical-protein
MNSCRSLSLSAASLYDIQTGWTRPIEHAWSMIARDHAAVFGQAPVQGSAASVVVRYAQEEDGCPEWPEAFSFRFSGSEAAPVLHIIGRDELGIIYGLLHYSRYILGVDPFWFWSELPPARRDSILVPVENVDSFQPKVRYRGWFVNDEVCLIGWKEQYPPGEEVWQPVFEALLRCGGNMVIPGTDLPRTGIHHSLAADMGLWITHHHAEPLGAEMFLRAFPGKQASYKEYPGLFEQLWREAIRKQKDEKVLWVLSFRGQGDKPFWENDPGFDTPEKRGALISSVVRKQYDMVSEAVPQPVCCMAMYGEITELYKQGYIEVPPGVIKIWADNGYGKMVSRRHGNLNLRVPALPSAGDNGKNGVYYHVTFHDLQASNHLTMFPAPAELIADELDQAFAAGADEYLLVNSGNILPHLYTLDLVAEQWATGCVKPEQQLQNFIGRYYTQQQEEIAGLYRSYPECTIAYGPNPDDRAGDEFYHHPARQIMGYWLRGQTAGDERLQWSAGSGTFLEQVRRFRERAEAAVPGWDTLRQRCVQVMEHLPEDEQHRLNHQLLVQIDLHLSGCRGLASICRAYEAYSGGHYPQAFIHASHAVWNYSEGKAALQRAEQGRWEHFYRADWLTNLDNTIQHADTVRRFVRIQGDSPDMFLWYKEYLMPETEKHIYLENTHRNPLSDDELAQRLESVFFL
>NZ_LN831776.1|WP_046505001.1|5636974_5638726_+|extracellular-solute-binding-protein
MTSKTAKPYMLLMVLTLLLSMLAGCSGSNNTKNTAENAAATKAAGEGNASATAEATAKTEDLSPLTLSFFAEDPNPNWNNMKDDISKVITEKTGVTLDAEFAVGDPQQKIALIAAGGEYPDIISAKADIGKLVDAGAVIDLTELIDKYAPNIKRVLGDNLARAKYTNEDQSIYAIPTWAAMNEKKFVAGGGFELQHRVVKEAGYPEIRTVADYEKVIKDYLEKHPTDENGNKNIGLSLNADDWHMYISVTNPAVATTGGSDDGEYYINQETHEAMYHFRRPEEKEYFRWLNHMNDIGLLDKESFVQKYDQYKAKVATGRVLGLIDQDWDYNDAQQALKTAGKFDQTYGHYPVTLTKEYKETSFWPTGFMGGYGISISSTNPDPVRTIKFLDYLASDEGQILNNWGIEGKHYTVENGKRVVIKEVQDRINNDNTAFTKESGLGFYWNIMVHYGDGAKDSTGNYYTRNFPEQLVLGYSDVEKETLAAYKATTWKDLFPKEEEFKEKAYGAAWNIAIPGEDEVSILGNKMRDITWKRIPQAILAKPADFDKIWEDYMADLDKAGVEKMEKGYTKYVQDRVALWTNK
>NZ_LN831776.1|WP_020426117.1|5635996_5636899_+|carbohydrate-ABC-transporter-permease
MLSKKLAAASWSDRIFDLVVYAAITVVTIATLYPFLNVLAISFNDSTDSIKGGITVYPRVFTVKNYETIFAYSGLMTGLKISILRTIIGTILGLVSASMLAFTLSRVDFQARRFVSTFLALTMYISGGLIPVYILIKNLNMMGTFGVYVLPGLVSAFNVFVIRSFIDGLPYALQESAKLDGANDFTIYWRVILPLTKPALATIALFLAVGQWNAWFDTYLYNGSKDGLTTLQFELMKVIQSTTTNADNFRGRNMTEVMAQISPESVKMAITIVVTVPILVVYPFLQRYFVKGMTLGSVKS
>NZ_LN831776.1|WP_020426118.1|5635029_5635986_+|sugar-ABC-transporter-permease
MKAITAKVQPEPKKPASRFWPKFLQQKYLYMMAVPFVLWAFVFNYLPLWGWTMAFQKYKPGKSFFEQKWVGLQYFRELFQDEQFFNALRNTLAMSLMGLLAGFIIPIVFAVLLNELRQIFLKRFVQTVSYLPHFVSWVVAAGIITKMLSTDNGAVNDLLMSLHLISEPIQFMAKGNLFWGIVTASDVWKETGWNTIIYLAAISGIGPELYEAARVDGASRLQQVRNITLPGIRTTVIILLIMSIGHLISIGFEKQFLLGNNLVRDYSQTLDLYALNYGLGLGRFSFGTAINIFNSVVSVFLLFVANGIFKKITKESII
>NZ_LN831776.1|WP_020431109.1|5654799_5656230_-|putative-basic-amino-acid-antiporter-YfcC
METVKSKWKWSLPHSYTLIFLIIIAIAGLTWIVPSGQFDRQEVVVDGSSRTAIIPGTYHTVPKISDQGDLRQGFAQIASAPMEGIINAADVVAFVLIVGGAFGIILQTGAIDRALMALAGRLKTKGILLIPIAMVIFSLGGSTFGMSEEIIPLYAIFIPLMFALGFDSITAILILFLGTQIGYVGSTVNPFSVLIAQGVAGVQGNPQLWLRFIEWTVFTGISVGFTMWYAHRVKKNPEKSAVFQNDILNRQHFIKENDGIEVKFSNRDKLIIGGFIVTLGIIVWGILSKGWYMTEIGALFFVLGIFSGIVTRMSQKEIAENFVKGCGEFIYAAVIIGLARGILVVAENGMIIDTILNGLATMLEGLPNYLFTTIMLVVHNVITFLVPSSSGEAALTMPVLAPLGDLVGVNREAVVTAYQFGNGLTNLISPTGGVLLAGLAIARINFGQWLKVILKLFPILWLVAAIFAAISSAVGM
>NZ_LN831776.1|WP_020431107.1|5656232_5657816_-|amidohydrolase-family-protein
MEAATHGFADRVLLSNAVFTGIEDSVSPAFVALQGERIAAVGNPAEAKDWIGPKTFVHHLKDALIMPGVHDNHVFFTGYMSMHRGVDLTHAATIDEALQLLRQDAENRPSEQNVYAYGWSEEGWGQLPGQSLLDEAFPDRAVIAINRTKSYCWMNTLAQHKYQFAPDECSAESRAHLLKDMMQDRELVRQEFLDFARMLAKRGVTSIKDIGFDRHSGLLPVLEELEAAGELPLRVHFALEPVLQPLDIPAGLQYKERYQGEFLRFQGYKLMLDGVVADHTGDMLEPYADMPGVTTLRPVDYEAIETAVQAADSHGIKCCLTAEGDAAIRKAVDILEGCSRRRGDQRIRHSISDLEYPHPDDIRRMGENGIFAEVYAQILLLNPSYEEAYMSAVAGKENESRFYNYKSMLEANVPVTIGTDLPLFLTSVPDSLYAASFRLFSDGSPMGGWQPEQGMPAAEVLKAWTINGARHNGMEERTGTLEAGKAADIAVFDRNLLDTTATEIRDAHVILTITAGQITYDAARNEG
>NZ_LN831776.1|WP_046505009.1|5657906_5658620_-|GntR-family-transcriptional-regulator
MLNSEQVEPLYIQLKKAVQAAIANGSFNPGDKIPTEIELSATYNVSRITVRKAIEELVSEGYLTKRQGKGTFVNAHKIGRKIEHIISFTAACRANGLSSHSVITERKKIKADQETAERLQIQQGEPVLYIQRKRYAGERPLMLENNYYPFERFSFLMEESLEGSVYELLRDRYQIDPNQPGETVLQITLADEQQAKLLEIPIGQPLFYMNTIIYDQHSKPVHVGKQYIIGDRYQFTL
>NZ_LN831776.1|WP_020431099.1|5658716_5659529_-|fructoselysine-6-kinase
MKVLGIGDNVVDKYVHQRTMYPGGNALNFSVFAKGEGAEAAFLGVFGDDDEARLVENTLQQLEIDISHCRHHSGENGCARVTLENGERIFLGSNEGGVTRLNPIMLSEADREYIRGFDLIHTGLYSHTGHLLAELNELGIPLSFDFSDDFEDEQVERYIGNADFAFFSCSHMTEEETRNFIQAKRRRDGQILVATRGGDSSIAYDGTAFYYQAPELIEAVDTMGAGDSYITAFLMSMIKDGNIQAAMQEGCRLAAKSCMVEGSFGFGARY
>NZ_LN831776.1|WP_046505012.1|5659544_5660513_-|SIS-domain-containing-protein
MNVNQVVQSIREKVAEGISEVYFVACGGSLVDMYPSKYFLDSEAKKLVAGLYTANEFVHALPKRLGAQSVVIVCSHGGNTPESVAAAQTAKEQGAHTIGLTHNKEAALLNYSDYSFLYEWGDDSNVKNNPMAIILDLAVQLLHVAEGYAHVEAFQKGLESINGIINQGKKQVAPRARVFADKYRNEELYYILTSGASYGHAYGFAICSLMEMQWLNAAAIHSGEYFHGPFEVTDKETPFILMMNEGRTRALDERAQTFLNQYAEKVEVIDAKELGIGTIADEVVEFFNPVLFYSIICVYREALAEVRNHPLETRRYMGKVAY
>NZ_LN831776.1|WP_020431094.1|5661066_5662437_-|HAMP-domain-containing-sensor-histidine-kinase
MIRSLYTRVVLTYLVSVIGGTIIALLVATWVYYDQFNENLKTNILYYGQDIVRMYESFPLQEVDTYLSGMKQLSYYIRVYDETGQFQSYGTLNGSRIPTITMDQVKAVLDGEVVQVSGVDKSLLGLPLKTETGKKALFVNSVAPPSATFFIKWLLNFVAFSLIAGSLIILVAAMFLVRPIKKLTKATRQIATGDFSVNLNIKQKGELGTLARSFEDMMHDLQQLEQMRRDFVSNVSHEVQSPLTSISGYAKALKQVNLAEQERSRYLDIIIAEAERMSKMSDGLLKLSLLESQSLQLRLSTFSLDEQIRRVIVAVQPQWSDRNIRFELHLEPVRLTADQDQLNQVWTNLIGNSIKFSKDGGVITVSIRQEFKNVTVRVSDTGIGISLEDQKRIFERFFKADRSHSRKYGGSGMGLAIVKQIISLHQGEIRVESEPGRGATVIVILPTTTPADKPDN
>NZ_LN831776.1|WP_020431092.1|5662433_5663108_-|response-regulator-transcription-factor
MPTILVADDDANIRELVSLFLRNDGFQTAEAADGEEALNVYASTQADLVVLDIMMPVMDGWTLCKELRRINPDLPLLMLTARGETWEKVKGFELGTDDYLTKPFDPLELTARVRALLKRYRIGSAQKIQFGNVILDRQTYKVMRGTESLTLPLKEFELLYKLAGTPGQVYTRGQLIDQIWGIDYAGDDRTIDVHIKRLRERFADTPDFRIETVRGLGYRLEAHE
>NZ_LN831776.1|WP_046505016.1|5663286_5663676_-|hypothetical-protein
MKRISILSISLIILLVVIFVLVRPKQEIVSVSLASETTQITYTDTESIQIFEDAIRSIKKVRGAVDVGPPTYRMTVTYADSEVVEFSLYIDLKTKNGFLIKDSDSEKMLDLRDKNSEELADLLSEVERE
>NZ_LN831776.1|WP_020427312.1|5664045_5665461_-|glucuronate-isomerase
MKAFIHEDFLLQTEEARVLYHEYAEALPIIDYHCHLDPQAIAENKRFGSITEVWLGGDHYKWRALRTFGVEEKYITGNASDEEKFAKWSEVLPYTLGNPLYHWSALELKTYFGVEEQLSPQNWRQIYDHCNTLIAQDGFTAQGLITRSNVKWICTTDDPADDLRYHGQIAGQPGFQTGVTPTFRPDKAMQIEAESFPDYVRSLEQAAGYAITSYALMERALLERIEYFDKHGCKVSDHGFSHLPFAEAAPSVLEDIFSRRLSGGTLSRLESDQYQTALLLAMGRKYAAHGWAMQLHIGAIRNPNSRMFRELGPDTGFDTIGDNSYANSLYKLLDGLERTGELPRTILYNLNAVQNDVLAAMAGSFQGGGIKGKIQFGSGWWYNDQKDGMIKQLTSLSNLGLLSCFVGMLTDSRSFLSYTRHEYFRRILCNLIGGWVASGDAPGDLAFLGSIVQDICYHNAERYFEFPLSRG
>NZ_LN831776.1|WP_046505020.1|5665537_5667148_-|mannitol-dehydrogenase-family-protein
MLRLTRSSIQQEQAAWTAAGVELPQFDYEQVAKNTQQKPEWIHFGAGNIFRGFVANAHQKLLDSGKAATGIIAAETFDFEMIDKVYKPYDNLTLLVLMNARGDFQKRIVNSIVEGITADKSREADDRRLTEVFENPSLQMASFTITEKGYSLTGPNGKYLGIVEKDIEGGPEQPVHAMSIVASLAYKRYLKGAFPMTFVSMDNCSHNGDKLKKGVVTIAKEWTARGLVEEGFVAYLENEQLIAFPLSMIDKITPRPSETVQAALLEQGIGGMDVIITSKNTYTAPFVNAEISEYLVIEDKFTNGRPLLEEAGIIFTDRDTVNNVETMKVTTCLNPLHTALAVSGCLLGYSLIADEMKDDTLRRFVEIIGYKEGLPVVVDPGILSPKQFLDEVLTERFANPFIPDTPQRIATDTSQKVGIRFGETIKSYIRREELDPAQLTAIPLAIAVWCRYLLGVNDEGEAFTLSPDPLLETLQGHLQGVALGDRNASVRPILEDEQLFGVPLYEIGLGSKIEGMFLEMLAGPGAVRRTLEKYLK

Crispr_ID: NZ_LN831776_60

• CRISPR_ID: NZ_LN831776_60
• CRISPR_location: 5681488-5681562
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_60

Consensus_repeat	Method
AAGTGGAAAAAGGGAACTTATTT	CRISPRCasFinder

spacers of NZ_LN831776_60

>60.1|5681511|29|NZ_LN831776|CRISPRCasFinder
CTTCTCAAAACTCAACAATTGAGAGATTT

CRISPR arrays and Neighbor proteins around NZ_LN831776_60

CRISPR arrays

The CRISPR arrays of NZ_LN831776_60

>merge|NZ_LN831776|60|5681488-5681562|CRISPRCasFinder
AAGTGGAAAAAGGGAACTTATTTCTTCTCAAAACTCAACAATTGAGAGATTTAAGTGGAAAAAGAGAACTTATTT

>NZ_LN831776|60|60|5681488-5681562|CRISPRCasFinder
AAGTGGAAAAAGGGAACTTATTT	CTTCTCAAAACTCAACAATTGAGAGATTT
AAGTGGAAAAAGAGAACTTATTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020427967.1|5692956_5694564_-|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_085981574.1|5682422_5682722_+|hypothetical-protein	unknown	unknown	gnl|CDD|379550
NZ_LN831776.1|WP_020427326.1|5674527_5675502_-|SIS-domain-containing-protein	unknown	unknown	gnl|CDD|225132
NZ_LN831776.1|WP_020427320.1|5670460_5670688_+|hypothetical-protein	unknown	unknown	gnl|CDD|378969
NZ_LN831776.1|WP_020427327.1|5675871_5676582_+|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225099
NZ_LN831776.1|WP_020428411.1|5683413_5683647_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046505055.1|5689551_5690988_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_LN831776.1|WP_020427321.1|5670859_5671273_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427325.1|5673621_5674488_-|fructoselysine-6-kinase	unknown	unknown	gnl|CDD|238915
NZ_LN831776.1|WP_046505030.1|5672224_5673544_-|anaerobic-C4-dicarboxylate-transporter	unknown	unknown	gnl|CDD|236503
NZ_LN831776.1|WP_020428417.1|5678937_5680017_-|LCP-family-protein	unknown	unknown	gnl|CDD|224235
NZ_LN831776.1|WP_020428416.1|5680475_5681444_+|bile-acid:sodium-symporter-family-protein	unknown	unknown	gnl|CDD|223462
NZ_LN831776.1|WP_020427322.1|5671325_5672156_-|sugar-phosphate-isomerase/epimerase	unknown	unknown	gnl|CDD|182116
NZ_LN831776.1|WP_082118188.1|5686520_5687678_-|DUF2961-domain-containing-protein	unknown	unknown	gnl|CDD|378582
NZ_LN831776.1|WP_020427964.1|5688534_5689470_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_046505052.1|5687704_5688538_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_046505027.1|5669885_5670251_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_039788180.1|5682884_5683340_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_052741516.1|5683901_5686178_+|hypothetical-protein	unknown	unknown	gnl|CDD|371926
NZ_LN831776.1|WP_020427966.1|5691160_5692948_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020427967.1|5692956_5694564_-|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.834e-43
NZ_LN831776.1|WP_085981574.1|5682422_5682722_+|hypothetical-protein	gnl|CDD|379550	pfam14310, Fn3-like, Fibronectin type III-like domain. This domain has a fibronectin type III-like structure. It is often found in association with pfam00933 and pfam01915. Its function is unknown.	5.5092e-26
NZ_LN831776.1|WP_020427326.1|5674527_5675502_-|SIS-domain-containing-protein	gnl|CDD|225132	COG2222, AgaS, Predicted phosphosugar isomerases [Cell envelope biogenesis, outer membrane].	1.37555e-111
NZ_LN831776.1|WP_020427320.1|5670460_5670688_+|hypothetical-protein	gnl|CDD|378969	pfam12841, YvrJ, YvrJ protein family. This family of short proteins are related to B. subtilis YvrJ protein. None of the members of this family have been functionally characterized.	0.000337229
NZ_LN831776.1|WP_020427327.1|5675871_5676582_+|GntR-family-transcriptional-regulator	gnl|CDD|225099	COG2188, PhnF, Transcriptional regulators [Transcription].	5.52999e-71
NZ_LN831776.1|WP_046505055.1|5689551_5690988_-|extracellular-solute-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	7.71841e-70
NZ_LN831776.1|WP_020427325.1|5673621_5674488_-|fructoselysine-6-kinase	gnl|CDD|238915	cd01940, Fructoselysine_kinase_like, Fructoselysine kinase-like. Fructoselysine is a fructoseamine formed by glycation, a non-enzymatic reaction of glucose with a primary amine followed by an Amadori rearrangement, resulting in a protein that is modified at the amino terminus and at the lysine side chains. Fructoseamines are typically metabolized by fructoseamine-3-kinase, especially in higher eukaryotes. In E. coli, fructoselysine kinase has been shown in vitro to catalyze the phosphorylation of fructoselysine. It is proposed that fructoselysine is released from glycated proteins during human digestion and is partly metabolized by bacteria in the hind gut using a protein such as fructoselysine kinase. This family is found only in bacterial sequences, and its oligomeric state is currently unknown.	1.32559e-101
NZ_LN831776.1|WP_046505030.1|5672224_5673544_-|anaerobic-C4-dicarboxylate-transporter	gnl|CDD|236503	PRK09412, PRK09412, anaerobic C4-dicarboxylate transporter; Reviewed.	3.55241e-177
NZ_LN831776.1|WP_020428417.1|5678937_5680017_-|LCP-family-protein	gnl|CDD|224235	COG1316, LytR, Transcriptional regulator [Transcription].	7.06789e-39
NZ_LN831776.1|WP_020428416.1|5680475_5681444_+|bile-acid:sodium-symporter-family-protein	gnl|CDD|223462	COG0385, COG0385, Predicted Na+-dependent transporter [General function prediction only].	4.99266e-52
NZ_LN831776.1|WP_020427322.1|5671325_5672156_-|sugar-phosphate-isomerase/epimerase	gnl|CDD|182116	PRK09856, PRK09856, fructoselysine 3-epimerase; Provisional.	6.26476e-37
NZ_LN831776.1|WP_082118188.1|5686520_5687678_-|DUF2961-domain-containing-protein	gnl|CDD|378582	pfam11175, DUF2961, Protein of unknown function (DUF2961). This family of proteins has no known function.	1.12021e-104
NZ_LN831776.1|WP_020427964.1|5688534_5689470_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	9.03376e-89
NZ_LN831776.1|WP_046505052.1|5687704_5688538_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	5.25162e-83
NZ_LN831776.1|WP_052741516.1|5683901_5686178_+|hypothetical-protein	gnl|CDD|371926	pfam12152, eIF_4G1, Eukaryotic translation initiation factor 4G1. This domain is found in eukaryotes, and is about 80 amino acids in length. It is found in association with pfam02854. This domain is part of the protein eIF_4G. It binds to eIF_4E by wrapping around its N terminal to form the eIF_4F complex. This complex binds various eIF_4E-BPs (binding proteins) to regulate initiation of translation.	0.00241575
NZ_LN831776.1|WP_020427966.1|5691160_5692948_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	2.19359e-58

Protein sequences

>NZ_LN831776.1|WP_020428416.1|5680475_5681444_+|bile-acid:sodium-symporter-family-protein
MLLAVNRTLNRMMPLITPLSVLTGVLCGSALSSYTYLSPWLFAFMTFAGSISLGFKDFVNVLKKPLPLFACLFILHIVMPLVALGIGNVLYHADEFTITGLVLAAVIPTGVSSFIWVSIYKGNTALTLSIILIDTLLAPFVVPGVLSLLIGTSVELDTGAMMSSLFWMIVVPSLLGMVLNEWTKGAVAPVWSPRLNPFSKLFMAAVIMINGSVISPYLADISLHLVGLAFVIVLLASTGYALCFLTARVLRWNEADEVALIFNGGMRNISAGAVLAVSYFPAPVAVPVVLGMVFQQLLASLAGFLLSHRAKVRHTAEQTTAA
>NZ_LN831776.1|WP_020428417.1|5678937_5680017_-|LCP-family-protein
MEERSKRMKAKRGKVRTRKTLLTLSAVLGTCLIAGAVYAGTLYYKAERALDRISAAGSAPGETAGPASPVPTASAAAAAVDAEEESKPLTFLLAGVDNRSGSGGTLNTDVLMPVVYEPVSRKLSILSIPRDMKIASSEMGTHKANYYYAYFYAHNKGEDLSKTREFYGDILQMDIDHMILVNFEAFSSIVDELGGLDIDVPMDMRYVDNADGTNINLTKGRQHLNGKKVLDFVRYRKSNRGTAESSDFSRNERQQEVLNLILDKLDSVSGIAKWGNIIDILGDNIRTDIGKDQLRSWILNYPSMKPAASELITLESGWKSPYVYANKEDLLVKLQKLREPLALPALDTRKLLHDFGIAE
>NZ_LN831776.1|WP_020427327.1|5675871_5676582_+|GntR-family-transcriptional-regulator
MLDHSESSPLYKQLQEKILDSIHDGTLKPGDKLPTELELSETNQVSRVTVRAALDALTSEGYLVRIPGKGTFITKDKIQKNVAETIGFSDTCRLQNKTPGAKVIKCVIEEATAADQEHLGLNPGDKVINIERIRYADNVPISVEYSRFPSSYSFLLQEDLNDKSLYEILRSKYKVTFGHSRKYIVMEYASFDVAAYLNIEEGYPLLSIRSTVSSPDGQKIHRSKQLILGDKFELIV
>NZ_LN831776.1|WP_020427326.1|5674527_5675502_-|SIS-domain-containing-protein
MDIKQIIEQITADKKEAGGIKQVYYAACGGSYGAFYPAKTFLEKEAKDIKVGLYNSNEFVHNTPKAFGENSVLVVASHKGNTPETVKAAELGKKAGVPVIALTWIEDSPITEYADYVVKYTFGENKDIAGEKTIQALMTAVEILKQTEGYGNYDKFLDGVSRIDRIVKQACKHVANRALTFARNHKDDSVIYTMASGAGYGAAYMESICIFMEMQWINSASIHSGEYFHGPFEITDAEIPFVIQVSEGSTRALDERALSFLNRYAKRVEVLDAKDLGLSTIDSSVVDYFNHSLFNNVYPVYNQALAVEREHPLTTRRYMWKVEY
>NZ_LN831776.1|WP_020427325.1|5673621_5674488_-|fructoselysine-6-kinase
MKQYKVIGIGDNVVDKYVHQGIMYPGGNALNFSVYATMCGMESAYLGKFGSDEVAGYIRQVIDELNIDRSCCREYEGENGYARVTLEDGDRVFLGSNKGGIAKEHAWQFTKKDLDYIKQFAVIHTSLNSYIEQDLTVLRESGVPISYDFSVRWNDGYLEQVCPNVDISFLSCSHLTAEEREREMRKAQRFGAKIVVGTVGENGSYALFSDQWIYHPAVSTEAVDTMGAGDSYITAFLVELIRNSDGRIEFGQESEMLGKIKSSMSKGAEFAAEICRVNGAFGFGTPLV
>NZ_LN831776.1|WP_046505030.1|5672224_5673544_-|anaerobic-C4-dicarboxylate-transporter
MFWLELLIIFLLIFFGARVGDVFMGLLGGVGVAIFVFIFHVQPASPPVDVMLIILGVVLAASALQSSSGLNFLVHVAEKLLHKSPKNITIVAPVICWLFTFLSGTGHVVYSLLPIINKLAIDSGIRPERPISNSIIASQQAITCSPVSAATAAMLGLMAPLGVGLGTILSIAIPATLLGVIVSALLTLRKGKELAEDPEYLRRLAEGLVESAPEEQPEKKATPKGAKASVVLFLLAVLSIVILGLFPDLRPSWTVDGVTTVLTMAHTIEIIMLVCASLIIIICRPAIETILNGTIFRAGALAMVCAFGLAWMSNTFIGGQTEFIQEHVAAVVNSQPWMLAVIMFIVAALTTSQGATTLIMIPIAIGLDLPAYIIVGAWMAVNANFFLPVSAQCLAAISFDTAGTTKIGRFVLNHSFMLPGMINIVVSVVTATLIGNVLI
>NZ_LN831776.1|WP_020427322.1|5671325_5672156_-|sugar-phosphate-isomerase/epimerase
MIQLNQVSAANFHYKRYSLDYFLDSAARLGFENIELWASGPHFHLDYYTPQDVQHLKRKIKDRGLKVICLTPEQSVYPISISHPDPVYRKKSVEFFCRHIEVAALMECDQMLVTTGLAYLDEDESEMWKWCRESLGEICKTAEKEGVILPVEAFTSYSTHVFNSAEHISRMIKEVGSPNLKGLADTDVMAVTGKDTIHDFIRELGGNLGYVHFVDGNPGGHLVPGEGGLPLEEALQALNDSGYKGYLGLELLDRRYVLDPEKAMRDSLAWFEKHLG
>NZ_LN831776.1|WP_020427321.1|5670859_5671273_-|hypothetical-protein
MKVDIYAYDGIGIQCVYKNDEWLVCIKNWKPDNDIDGIHRLEVHLETDEQFILVNGKAILLVADRKKDQFDIDLIEMEIGKVYNVPKNTWFYTIVQKDTKLAYVQHANTTEENSSYCEMSESELAGVKERARKILKL
>NZ_LN831776.1|WP_020427320.1|5670460_5670688_+|hypothetical-protein
MDLQSLVQLVGNVGFPIALSIILLQTILVTFNRQVEGLEKRLSQLEKTMNMLVKTFHQSALRVPPQGQKKEESKD
>NZ_LN831776.1|WP_046505027.1|5669885_5670251_-|hypothetical-protein
MKYSINLFGYSVDCELKLVGEGLSIEITEENQKALKQYLVRVLPKYGREATSESSFQTLLELAIDAEKTLDGRMVEPKLKLPYEFQPEIKEKLIEAAALQDVSATQLLIRIIEKKYQEVMG
>NZ_LN831776.1|WP_085981574.1|5682422_5682722_+|hypothetical-protein
MISGTVFCRQEISDIAGKETVQLYIRDVSASVVRPVKELKGFRQLSLAAHEKQRVSFEITRDLLMFYVKDDQLIFEPGEFDIMIGRNSGDHETQRIWIG
>NZ_LN831776.1|WP_039788180.1|5682884_5683340_+|hypothetical-protein
MEDQLFHQTVNELLALSNSKVQVILEPRFQDNRLVGGKYHLASHTIFLYKEEIVRQCCELFGSPLRLKEYIAVVLAHELGHSEDQELELLAAALDRPLTEKQEAEIRLRIEENAWAYAVSLLTEADPTFLRFIMDESLFSYRDRLDRFHIA
>NZ_LN831776.1|WP_020428411.1|5683413_5683647_-|hypothetical-protein
MAQNNQNDQKMSREEAGRKGGEATAKNHDREFYQEIGEKGGEARSRNQSGSNGNDGKMSREEAGRKGGEARTRQRDN
>NZ_LN831776.1|WP_052741516.1|5683901_5686178_+|hypothetical-protein
MPHPFTTISEALSQSRSSSFGVVYKNGKFTANDPLSFFGRKLPDPELTFDTANNKTLVNVHMNGSIKNVTVYNGSYSSDNIPGVWMCKDFREAGPYAYSLELGGLHYHLGSDDLAYSTSLLDNLFPVTEYQLGAIKATLLVYTPVSADGSQRLRGLVYGLQLENQSGQTIAGQVTPPPADTLPDQLFSGPEFCVHVPGHKVDVNGTVPVSLAPGQTLWVPAVIYPAGDPCPRIIGEKGTLYWLNETWAYFRGITGRLTMEEDPFAAEFYERALLQCFGSLAMDSRGSLAGANWGTSPPTQFTWNKDMFYSLLPFHTAEPELFQQGMLWFLEHGVRPPGNRYEGGITHSLSNSLSSVVMAGLYYRTTGDKQLFWNRSGIHESICSLLEATLLTRKEEDPWLFPSVWLSDAYSLGDYHTGSNVIAWTAFVHYARIAEEVFGDTARAERYRTIAGRIRADLERLATAEGPFGLQYAEGISSSGDKLKDNAGKYTGKYADFGMQFIENLTAEGQINLLHHDGEESDTILMPLYGYTSYDNETYRHYMQFSLSPHNPTYNPESRGIQWGDHSACTFPGYMSGMGMITDAASLSGEDGYLTRIRQLTDADGSLWWWPYNNGAAYGDVVRHNNCGKCGWASGVFAGLFVSEILGLAYDASARQLSFRPLSPSSSFTWEHVKLGSGSFSVAYRKTDSSVEASIQNLCTKTVTVCVELRHDNARRLEPFARTGDKELAAHAEWSDRAASRRFKKTLEPGRAVTFGLR
>NZ_LN831776.1|WP_082118188.1|5686520_5687678_-|DUF2961-domain-containing-protein
MNSLYLRKEGLSRRQSSWDQTGGNRDFIVIGAGQTAAIAEIEGSGIIQHIWMTIAAKNKYAFRKVLVRMFWDGEEEPSVESPVGDFFGVGHGVASHYVSMPLNMITTQGVIEDKAAMNCFFEMPFRSSARIEIINECEDEMVLYFYVDYVEKEIPEDSFYFHASWRRENPTQGTVDLAALKLEHDRQDKANYADQKVYEVKNLTGDGNYVLMDAVGEGHYVGCNLSIDHLNPMPGFSWPGEGDDMFFIDGEPWPPRLHGTGTEDYFCAAWGYPSGKYDSPYHGVSLYAPIRGNGDAWRESNTILFNDYSGKMTQYRFHIVDPVIFRESLRFSIEHGHGNSQSNDYSSVAYWYQREPHKSYPEMLPVHLRLPLPEKESAKQFYRTF
>NZ_LN831776.1|WP_046505052.1|5687704_5688538_-|carbohydrate-ABC-transporter-permease
MRAKAWVEKGLVYLVLVAGGLFSLLPLIWLIRSSLMDMGQIFELPPIWIPDPFRFGNFSEALTILPFGRYFINTTVIVIFTMLGVLVTCSISAYSFARMSWRGRNLVFGLLLSSMMLPYAVTLIPTFIGWSKLGLTNSFIPLIAPAWFGGGAFNIFLLRQFYLSIPRDLDEAAYVDGASHWRIFISIIIPLTRPALVVVGLFTFLASWNDFLGPLVYLNSESKYTLALGLQQFKGMYAAEWHLMMAAATVVLAPAIVVFFIGQRYFIEGITLTGIKA
>NZ_LN831776.1|WP_020427964.1|5688534_5689470_-|sugar-ABC-transporter-permease
MEPVPSLSVNRPKTKRSSYKNELYGILFALPAILGLLIFTLGPMIYSLYMSFTDYSGSNSPTFIGLDNYTRMFSGEDQYFYKSLGVTLYFVVLSVPTGIIYSFLLAILLNRNIKGKAIFRTVFYLPSIVPIIAISFIWLWLLNPDLGLANEMLRAIGLPGSQWIFGEKSVVPSLALMNLWTTGGTMIIFLAGLQDIPRSLYEAIEIDGGSKLHKLRNITIPMMTPTIFFNLIMGIINGFQVFSQAYVMTSGGPNNASLFYVFYLYREAFQFSRMGSASAIAWVLFIIIMLLTYMVFKSSKKWVYYEGDEAR
>NZ_LN831776.1|WP_046505055.1|5689551_5690988_-|extracellular-solute-binding-protein
MRKYTGRTKLMLLFLLIMALIVTACGAGGNNTNTAANTSKGNAKEGNSPAAGETGSAGGDKVTLKFTFWGSPQEKQAVEDAIKAFEAKNPNITIDSIHIPGTDFLQKLNAMIAGNEAPDLSYSAAWKLKMGEEGLIYNFFDLMKDDPSIKKEDYLQYAWWNWDTDKSAGPYQASVVPSLMYNADLFKEAGVELPPTKAEEAWQWDEFVDTAKKLTLDRNGKHPDDPGFDPKNIKQYGVKFSLSWLSYMPLVLSNGGDYLTKDGKEFGLSKPEATEAIQRIADLINVYHVAPSPVQASSIPAPATALQSRKVAMVIDGSWNHLDLSKANINWGVGVLPVLKDYKTFFLGGSLIIFKSSKHPKEAWEFSKFLTDPQNVLELHQGLWMPQLKQWYEDPKLVDSWANEKLPGRPAGFQDAVMRSTYEHAEPSAENNVRNFVEIDAAVTAGLDQVWLGTKTAAEAMKEVEAKVKPLVKGTYLK
>NZ_LN831776.1|WP_020427966.1|5691160_5692948_-|sensor-histidine-kinase
MKLKNKLILSYIVLITLPLTILGFGYYYASKEIMLKLARDNVSEIVLKNNQIINERLKIIQDDSLSLMVECQLYQIFDGSGPAGGQQLLATNKKVTEILGRYFSPSADLYSAELVTRAFVYGNKNKNTYPPDHFYSSELYRAAAEGKGRIAWVPTYDYTRMHALPELAGSNIEYRYMFSAVRQINPSCVRNDSIVRASPGSEKPVLVMNFKDDVYANIFRDSIPIQGSVFLVASENGTMIAHQDKMRIGTVEPAAWLKELRSKGSGTAYVTAGGKRMIACFALSPVTNWLSVVLIPPGALTHDIADTILFFILALGAPLLALSLLFAYLISARISSPVSKLLLAIKRVGGGDFNAQIKVEGRDELGHVLMKFNSMNEQVRELINENYVVKLRERETEILALNIQLNPHFLYNTLNIINWMAVYGEKEQVSNMLISLSRMLHYTTDNRRDLMLLREDIAWLQDYIVIMANRFEHRFRVDFDIQPELLEVSVPKLFLQPLVENAIIHGFRNMESGGLITIYGQRQGDDIRFCVEDNGSGIEPERLEQLLKAESPNIGLKNVDKRIKLLYGGKHGIEIESVPEFGTRVKLVIPYPGSE
>NZ_LN831776.1|WP_020427967.1|5692956_5694564_-|response-regulator
MYNVLVADDEPRHRRGIADMIKQLRPEYRIFMVKDGLEALRIIEDNRIDIILTDIRMPNMDGLTLIERMESRRERVKIVILSVYGNFEYARQALQLGAFDYLLKPLAFPELSGILDKLDTALEKERLSLQDGAVLRQRLSSAAPVYEQHLLSRWMRSASSEEELQEIRSLFPAVSGGFVMLAKFQKREVAEFYTLEDFEELKTSVINWMKEIYQTVGPSLSFNLEGADPMIGSIVTSAHSLEWLLKRDMEQFRQFIRQVRDEFGLTLTLGAGNWVADLYSEAPQSFEQAQKALEYTFYTGAGQLVLFDEIAYNPDKPSLKMVPADTGITDALARLDRDTVAQALKTLIGRLLEGDCPSPAHLKDCVLYALVNEVKGSELFLRQEEVSNFISEMEFQIPACESLDEVEKRAAFYLNRIMDSIGERKENKSGRTISLCKAFLEAHYMEDLSLEYVARQFFFSPAYFSSFFKQHTSLTFTEYLLRLRMDKAKELLQNGDLKISAIALSVGFRDAGYFTRVFKRETGLSPEEFRKKDVL

Crispr_ID: NZ_LN831776_61

• CRISPR_ID: NZ_LN831776_61
• CRISPR_location: 6014818-6014910
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_61

Consensus_repeat	Method
CTTCGGAAGCATACGCTTAAGTTTTGT	CRISPRCasFinder

spacers of NZ_LN831776_61

>61.1|6014845|39|NZ_LN831776|CRISPRCasFinder
GAGCCTATGCATCATCCGAATCGCTTCTTACAAAACTTT

CRISPR arrays and Neighbor proteins around NZ_LN831776_61

CRISPR arrays

The CRISPR arrays of NZ_LN831776_61

>merge|NZ_LN831776|61|6014818-6014910|CRISPRCasFinder
CTTCGGAAGCATACGCTTAAGTTTTGTGAGCCTATGCATCATCCGAATCGCTTCTTACAAAACTTTCTTCGGAAGCATACGCTTAAGTTTTGT

>NZ_LN831776|61|61|6014818-6014910|CRISPRCasFinder
CTTCGGAAGCATACGCTTAAGTTTTGT	GAGCCTATGCATCATCCGAATCGCTTCTTACAAAACTTT
CTTCGGAAGCATACGCTTAAGTTTTGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020426383.1|6008627_6010706_-|glycine--tRNA-ligase-subunit-beta	unknown	unknown	gnl|CDD|234925
NZ_LN831776.1|WP_046505282.1|6020850_6021450_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_039785724.1|6006092_6007913_-|DNA-primase	unknown	unknown	gnl|CDD|235551
NZ_LN831776.1|WP_020426381.1|6012024_6012780_-|DNA-repair-protein-RecO	unknown	unknown	gnl|CDD|273175
NZ_LN831776.1|WP_020426373.1|6019155_6020337_-|sporulation-protein-YqfD	unknown	unknown	gnl|CDD|377731
NZ_LN831776.1|WP_020426380.1|6012816_6012960_-|YqzL-family-protein	unknown	unknown	gnl|CDD|379412
NZ_LN831776.1|WP_020426377.1|6015006_6015402_-|diacylglycerol-kinase-family-protein	unknown	unknown	gnl|CDD|260134
NZ_LN831776.1|WP_020426382.1|6010698_6011586_-|glycine--tRNA-ligase-subunit-alpha	unknown	unknown	gnl|CDD|236473
NZ_LN831776.1|WP_020426386.1|6004918_6006052_-|RNA-polymerase-sigma-factor-RpoD	unknown	unknown	gnl|CDD|236413
NZ_LN831776.1|WP_020426374.1|6018168_6019140_-|PhoH-family-protein	unknown	unknown	gnl|CDD|224616
NZ_LN831776.1|WP_085981509.1|6007952_6008426_-|DUF188-domain-containing-protein	unknown	unknown	gnl|CDD|178882
NZ_LN831776.1|WP_020426367.1|6024141_6024585_-|GatB/YqeY-domain-containing-protein	unknown	unknown	gnl|CDD|370480
NZ_LN831776.1|WP_020426375.1|6015895_6018151_-|HDIG-domain-containing-protein	unknown	unknown	gnl|CDD|224397
NZ_LN831776.1|WP_020426379.1|6013067_6013961_-|GTPase-Era	unknown	unknown	gnl|CDD|234624
NZ_LN831776.1|WP_020426376.1|6015401_6015899_-|rRNA-maturation-RNase-YbeY	unknown	unknown	gnl|CDD|376735
NZ_LN831776.1|WP_020426372.1|6020333_6020627_-|sporulation-protein-YqfC	unknown	unknown	gnl|CDD|131903
NZ_LN831776.1|WP_085981507.1|6022507_6023842_-|nodulation-protein-NfeD	unknown	unknown	gnl|CDD|223961
NZ_LN831776.1|WP_020426387.1|6004007_6004832_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426378.1|6014335_6014755_-|cytidine-deaminase	unknown	unknown	gnl|CDD|183511
NZ_LN831776.1|WP_167330827.1|6021466_6022465_-|flotillin-like-protein-FloA	unknown	unknown	gnl|CDD|237462

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020426383.1|6008627_6010706_-|glycine--tRNA-ligase-subunit-beta	gnl|CDD|234925	PRK01233, glyS, glycyl-tRNA synthetase subunit beta; Validated.	0
NZ_LN831776.1|WP_039785724.1|6006092_6007913_-|DNA-primase	gnl|CDD|235551	PRK05667, dnaG, DNA primase; Validated.	0
NZ_LN831776.1|WP_020426381.1|6012024_6012780_-|DNA-repair-protein-RecO	gnl|CDD|273175	TIGR00613, DNA_repair_protein_RecO, DNA repair protein RecO. All proteins in this family for which functions are known are DNA binding proteins that are involved in the initiation of recombination or recombinational repair. [DNA metabolism, DNA replication, recombination, and repair].	3.04941e-73
NZ_LN831776.1|WP_020426373.1|6019155_6020337_-|sporulation-protein-YqfD	gnl|CDD|377731	pfam06898, YqfD, Putative stage IV sporulation protein YqfD. This family consists of several putative bacterial stage IV sporulation (SpoIV) proteins. YqfD of Bacillus subtilis is known to be essential for efficient sporulation although its exact function is unknown.	6.83761e-133
NZ_LN831776.1|WP_020426380.1|6012816_6012960_-|YqzL-family-protein	gnl|CDD|379412	pfam14006, YqzL, YqzL-like protein. The YqzL-like protein family includes the B. subtilis YqzL protein, which is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are approximately 50 amino acids in length.	4.91081e-08
NZ_LN831776.1|WP_020426377.1|6015006_6015402_-|diacylglycerol-kinase-family-protein	gnl|CDD|260134	cd14265, UDPK_IM_like, Integral membrane undecaprenol kinase and similar enzymes. This mostly bacterial family of homo-trimeric integral membrane enzymes, the products of the dgkA gene, catalyzes the ATP-dependent phosphorylation of undecaprenol to undecaprenyl phosphate. C55-isoprenyl (undecaprenyl) pyroposphate acts as a scaffold for the assembly of peptidoglycan components; undecaprenol kinase (UDPK) is involved in recycling undecaprenyl units for re-use in the peptidoglycan biosynthesis. UDPK does not participate in the de-novo biosynthesis of undecaprenyl phosphate. Gram-positive bacteria have a large pool of free undecaprenol, in contrast to gram-negative bacteria. UDPK may also play a role in a stress-induced pathway that affects the function of ribosomes. In Streptococcus mutans, UDPK has been shown to be required for biofilm formation, such as in the case of smooth surface dental caries. Members of the UDPK family have low activity as diacylglycerol kinases (DAGK), and many of them are annotated as DAGKs.	8.93582e-43
NZ_LN831776.1|WP_020426382.1|6010698_6011586_-|glycine--tRNA-ligase-subunit-alpha	gnl|CDD|236473	PRK09348, glyQ, glycyl-tRNA synthetase subunit alpha; Validated.	0
NZ_LN831776.1|WP_020426386.1|6004918_6006052_-|RNA-polymerase-sigma-factor-RpoD	gnl|CDD|236413	PRK09210, PRK09210, RNA polymerase sigma factor RpoD; Validated.	0
NZ_LN831776.1|WP_020426374.1|6018168_6019140_-|PhoH-family-protein	gnl|CDD|224616	COG1702, PhoH, Phosphate starvation-inducible protein PhoH, predicted ATPase [Signal transduction mechanisms].	1.25593e-141
NZ_LN831776.1|WP_085981509.1|6007952_6008426_-|DUF188-domain-containing-protein	gnl|CDD|178882	PRK00124, PRK00124, YaiI/YqxD family protein.	1.29151e-46
NZ_LN831776.1|WP_020426367.1|6024141_6024585_-|GatB/YqeY-domain-containing-protein	gnl|CDD|370480	pfam09424, YqeY, Yqey-like protein. The function of this domain found in the YqeY protein is uncertain.	2.98514e-62
NZ_LN831776.1|WP_020426375.1|6015895_6018151_-|HDIG-domain-containing-protein	gnl|CDD|224397	COG1480, COG1480, Predicted membrane-associated HD superfamily hydrolase [General function prediction only].	0
NZ_LN831776.1|WP_020426379.1|6013067_6013961_-|GTPase-Era	gnl|CDD|234624	PRK00089, era, GTPase Era; Reviewed.	0
NZ_LN831776.1|WP_020426376.1|6015401_6015899_-|rRNA-maturation-RNase-YbeY	gnl|CDD|376735	pfam02130, UPF0054, Uncharacterized protein family UPF0054.	3.9341e-52
NZ_LN831776.1|WP_020426372.1|6020333_6020627_-|sporulation-protein-YqfC	gnl|CDD|131903	TIGR02856, Uncharacterized_protein_YqfC, sporulation protein YqfC. This small protein, designated YqfC in Bacillus subtilis, is both restricted to and universal in sporulating species of the Firmcutes, such as Bacillus subtilis and Clostridium perfringens. It is part of the sigma(E)-controlled regulon, and its mutation leads to a sporulation defect. [Cellular processes, Sporulation and germination].	8.20981e-23
NZ_LN831776.1|WP_085981507.1|6022507_6023842_-|nodulation-protein-NfeD	gnl|CDD|223961	COG1030, NfeD, Membrane-bound serine protease (ClpP class) [Posttranslational modification, protein turnover, chaperones].	2.55734e-78
NZ_LN831776.1|WP_020426378.1|6014335_6014755_-|cytidine-deaminase	gnl|CDD|183511	PRK12411, PRK12411, cytidine deaminase; Provisional.	5.3691e-63
NZ_LN831776.1|WP_167330827.1|6021466_6022465_-|flotillin-like-protein-FloA	gnl|CDD|237462	PRK13665, PRK13665, hypothetical protein; Provisional.	0

Protein sequences

>NZ_LN831776.1|WP_020426378.1|6014335_6014755_-|cytidine-deaminase
MESALLLQEAIKARANAYIPYSRFGVGAALLDQDGHVHHGCNVENAAFGPTNCAERTALFRAIADGHKAGTFKAIAVIADTDGPVSPCGVCRQVMVELCAPDMKVILGNLRGDIQETTVRDLLPGAFGPTDLEQGQAPE
>NZ_LN831776.1|WP_020426379.1|6013067_6013961_-|GTPase-Era
MKFKSGFVAIIGRPNVGKSTLMNQVIGQKIAIMSDKPQTTRNKIHGVYTANNSQIVFLDTPGIHKRQSKLGDYMNQTAMSTLHEVEAVLFLVDASEGMGGGDRYIAEQLKDVKTPVILVMNKIDKIEPEALLPLITEYNKLHEFAEIVPISAKLGSNVNTLLDQVVKYLPEGPQYYPEDQITDHPEQFVCAELIREKILHLTREEVPHSIAVAIEDMRVESNGVVHVSAVIFVERDSQKGIIIGKQGAMLKEVGRRARTDIENLLGSKIFLELWVKVKKDWRNQERVLRDLGFHKDL
>NZ_LN831776.1|WP_020426380.1|6012816_6012960_-|YqzL-family-protein
MRDFSWKYFAMTGDVDAYLLYKQAADPLEGSLELPAEEEKVLDEEAQ
>NZ_LN831776.1|WP_020426381.1|6012024_6012780_-|DNA-repair-protein-RecO
MLYRVEGIVIRSMDYGEGNAIITLCTENAGKVGVLVRGAKKVKSRHAALIQLFTAGEYVFFRNNGGLGTLNAGEITKSHHPLREDLVKAAYASYACELLDRVLHDEETGSFWFRQLTACLNALEEDKEPGIIINVFEMKILQAAGYGPQLDNCIVCGLDKPDEELRVSPRLGGVLCRSCRHNDPPAMEISPRALKLLRLFAALDLTRLGNVNVKEGTRAELKKIMRAFMDHQLGLKLKSQNFLDQLDKYNI
>NZ_LN831776.1|WP_020426382.1|6010698_6011586_-|glycine--tRNA-ligase-subunit-alpha
MNFQQMILTLQQFWSAQNCILVQPYDTEKGAGTMNPMTFLRSLGPEPWKVAYVEPSRRPSDGRYGENPNRLYQHHQFQVIIKPSPDNIQELYLDSLKALGVDPLLHDIRFVEDNWENPSLGCAGLGWEVWLDGMEITQFTYFQQVGGIETSPVAVEITYGMERLASYIQEKENVFDLEWVGGMTYGDVFHQPEVEHSTYTFEVSDVKMLFTLFNTYEEEARRAMEQHLVFPAYDYVLKCSHTFNLLDARGAISVTERTGFITRVRNLARTVAATYLEEREKLGFPLLKKEGADLV
>NZ_LN831776.1|WP_020426383.1|6008627_6010706_-|glycine--tRNA-ligase-subunit-beta
MSKDILFEIGLEEVPARFIRAAMEQLKDRTVKWLEASRISHSGVTAYATPRRLAVLVKDAAEKQEDISEEVKGPSRKIALDASGEWSKAALGFARSQGVSPEQFTFKELAGVEYIYATKNSEGVNTSSLLSEGLSGIVSAMTFPKNMRWGAYDFKFVRPIRWLVALFGQEVIDLEITGVKAGNVSRGHRFLGTEAVIAEPAKYVETMRSQHVLVDVKEREELILSQINKLAEEKGWTIAIKDDLLEEVLFLVETPTVLFGTFDAAFLNIPQDVLITSMREHQRYFPVFDAAGALLSFFVTVRNGNAESLDVIARGNEKVLRARLSDAKFFYEEDQKLQISDALAKLENIVYHEELGSVGDKVRRIRAVADRLTVKLGLSAKTAAEVSRTADICKFDLVTQMVNEFSELQGTMGEDYARKAGEPEAVARGIFEHYQPRFAGDAVPASEVGLVVSLADKIDTIVGCFSIGIIPTGSQDPYALRRQAAGIVQMVLEHKLTVSLEEIFDAALEVHENLRTEKPFAPDLRINLYEFFGLRVKRLLSDNVRYDVVDAVIAAGFDDIVAVVGRSRALMDTVNSQADFKITVDSLTRVSNLAAKAAEGTAVAPSLLKEEAERKLYETWQAIHSPYQEALRARNAEEALRILSGLKDAVTGFFDSVMVMAEDEQIRANRLALLAGIDADSKAFADFGKLVW
>NZ_LN831776.1|WP_085981509.1|6007952_6008426_-|DUF188-domain-containing-protein
MERSQERKIVVDGDACPVKAEIIAVARSFGIPVIMVSSYDHVLRGEEGVSIVQVDRGADSADLYIANHITAGDIVVTQDYGLAALALGKRCRVLSNRGQEYDDLGMDFMLESRHARAVERRRGHYSKGPKAITAEEKIYFQHKLTKLLMILQENVQL
>NZ_LN831776.1|WP_039785724.1|6006092_6007913_-|DNA-primase
MASGQGNIPEEVIESVLARHDIVDTVGKVVHLSKQGKYLWGLCPFHSEKTPSFTVTPERGVFHCFGCGMGGNAIKFRMEIEGLSFPEAVRIMAEESDIPVPEGTGGVLSPPDPERDRLIQAYELSAKFYHFLLKNTEYGTAAMDYLRSRGFSGKMIDQFQIGYAPDRWDTLLQFLDKRSFNLAEMEKGGLLSARGEGKGYIDRFRGRVIFPIANRTGKVIAFAGRILGDGQPKYLNSPESRLFNKSRILYNLHQSKASIRKTRQIVLFEGYGDVISAWEAGVHNGVATMGTSLTEGHVALMKSLGDEIVLAYDGDKAGQAAAMKAIPMLEDNGLRVKVAVLPSGLDPDEFISRHGGERFKEQVIDSAVSSIKFKLIYLKKNHILLEEDGKIAYVKEALEIIASLHSSTEREVYLREIASELELSYDSLKQDCNLLRASMQKNLPEGDNNDKRWNNGRHKKGQVQAPTLLPAYHVAERRLLSWMIQDPDAAAYVGERLGEEFNIDDHAAIAAYLYAYYAQGKPPGISRFLSSLQDDRLEKTATAISMMDTPPDWNTQVLDDCIREVRKYPVQRGMEQKREEMIQAEKSGDFLRAAQIASEIIALERQ
>NZ_LN831776.1|WP_020426386.1|6004918_6006052_-|RNA-polymerase-sigma-factor-RpoD
MANDQHTELEAEFTLDQVKDQLIEQGKKRSSLNYKDIMEKLSPFDQDPEQMEEFYEQLSDLGIEVVNENDEEVNTLRPSEDNEGSDNDDFSFDDDLSLPPGIKINDPVRMYLKEIGRVPLLSADDEVELAMRIKNGDEEAKRRLAEANLRLVVSIAKRYVGRGMLFLDLIQEGNMGLIKAVEKFDHNKGFKFSTYATWWIRQAITRAIADQARTIRIPVHMVETINKLIRVSRQLLQELGREPSPEEIAAEMELTVEKVREIMKIAQEPVSLETPIGEEDDSHLGDFIEDQEALAPADAAAYELLKEQLEDVLDTLTEREENVLRLRFGLDDGRTRTLEEVGKVFGVTRERIRQIEAKALRKLRHPSRSKRLKDFLE
>NZ_LN831776.1|WP_020426387.1|6004007_6004832_-|hypothetical-protein
MNLEKREIILREIQYWRRSKVLPEQYCDFLTNLYDDEAGVKDSNPISLRNLQQGSIKVWLFGFGIISLIFLISLYFSVFPWPLQLATALCVLIVCYGYSYIYRDRNNMISLVLAGIGSVLTLGFGLWLIALHDLDPDFWRPLLIAGCGLLWVVLGFFLRISLLHFCGFAFWALLYAGFFGQQRPDASILELELLYLPLCVLMVWLSWLLHHRVNGVSGVYLGVGVSLWIMPEVDALLLRQDFPQWVSLILILKIAAGLALLFIFRKKWITWVTS
>NZ_LN831776.1|WP_020426377.1|6015006_6015402_-|diacylglycerol-kinase-family-protein
MVKNTAVGHKKFWHSFRFAAHGIASAFKSELNMKVHSTLAVLVLAAAVILRLPPSSWMLLLLAITLVLAAELLNTAIEATIDLVSPEIHPLAKKAKDTAAGAVLLTAVFAAIVGIYVFYHPVMDWITGLMS
>NZ_LN831776.1|WP_020426376.1|6015401_6015899_-|rRNA-maturation-RNase-YbeY
MSLAIVWNNEQEEHPISDELITLLESILQKAGEAEGIDEGEVDLTFVNNERIHELNLEYRGIDRPTDVLSFAMNETGEDEPEIIYALEEDEEGEDVPYVLGDIIISVTRAQEQALEYGHSLERELGFLFVHGFLHLLGYDHQDAVSEAEMMSKQEKVLAQVGLTR
>NZ_LN831776.1|WP_020426375.1|6015895_6018151_-|HDIG-domain-containing-protein
MASKQPSKLSGFVYNSNGWKYSAVTRYALFLLLGLVFYFSLSSDLVPKKYDIKEGTHSAKEITAPKQILDTKAKLKAQEEAAENVTNRYAIIPMRADTLVTSLLDRIDRLNQDDLISQSDKTAIYREEIPQRASDFILNFVASSRNAGTYSDTLLDEMQSVIKDQTYVIPEETYIKIPRLTSQDIIEMKPVARDIVTKLMNDQITDAQSARAKVAEQVSVSSLSQRTAREVVQELVRLVITSNKFYDEEATKEAKVQARENTPDVFIEQGDVLVAKGELITPELYTLLDDNGLLSNEVNYWPQFGLLILSALLSFGLFTFIRYSGGASGFKYNNSQLLMLVLVFIITIITVKLAAFLQTDARAYVGFLAPVAIGAMLITMLLDMSLAYFCSILFSILASIMLNVQQNTIFDFTFGFFALIVSYVAIFATHRAGQRSTLLKGGIMVSLIGSVTVFMLNVLAGGVWNQTQALYAIGFSFASGLLTAVLVIGLMPFFEATFGILSALKLVELSNPNHPLLRKLLTETPGTYHHSVMVGNLSEAAAEAIGADGLLCRVGSYYHDIGKTKRPFYFIENQNNMENPHDSIEPMLSKSIIVAHARDGVEMLKEYKLPKPIRDIAEQHHGTTFLHYFYHKALKLAEEKGVEPDFTEEDFRYPGPKAQSKESAVVGIADSVEAAVRSLRKPTVVQVETMIEKIIKSRLDDHQFDECDLTIKELDIIARTLKETVMGIFHSRIEYPEDVKKPKKEEGAVTT
>NZ_LN831776.1|WP_020426374.1|6018168_6019140_-|PhoH-family-protein
MSEQTASIRISLQNAGEAQSLFGPQDGFLKIIESEIPAVIDSREAEITIRGAEREVDMLGQLFGVLLSLIRSGYILSERDIQYAVELAKDFRADQLLDLFKGEITTTFRGKPIRVKTIGQKHYVTTIKKRDIVFGIGPAGTGKTYLAVVLAVTALKEGSVKRIVLTRPAVEAGESLGFLPGDLQEKVDPYLRPLYDALYDVMGPDQVAKALERGLIEIAPLAYMRGRTLDDSFIILDEAQNTTPEQMKMFLTRLGFGSKMVITGDVTQIDLPRGKKSGLIEAKTILSGIDELGFVYFAEQDVVRHSLVQKIIVAYERSAENLE
>NZ_LN831776.1|WP_020426373.1|6019155_6020337_-|sporulation-protein-YqfD
MKQPPLASLRGFVTLHVTGPQVEKFINAVTEADIVIWDVRPAGDGASLNLLLDDFFALRPLLKKTGCRTRVTARNGLPFNAAKLWKRKFFAAGLLLFGIGLVLLSSMIWTVQIEGNDRINSEDILQAARHEGVYPFQWIWRMDDPDKLSKKLTSTLPGVSWVGVQRTGTSVKIHIVESDQPENKPLLSKRHLISRTDAVVTEIYAEQGRPVVTRNTRVKKGQILISGAIGDEENMEYVVAKGEVKGLVWHEYNIEVPLNRTRSSYTGERKDRTYLVLGKWAVQLWGYGKADFAESRTLTEHDPLTWRSFQLPLGLLTEKEMEVLDTAETLTPEAAREEGITRAKNDILARYGTDSVIKSQKILHEKKENGKVYMKVLFEVEERITQELPIVNN
>NZ_LN831776.1|WP_020426372.1|6020333_6020627_-|sporulation-protein-YqfC
MTRIGRRLRGWTNGVLDLPQDVLQELPRITLIGNKELYIENHRGVLHFSSEQLRLALVNGSLEISGEGLVIRNILGQELAVEGIIGEIRYKGSEENS
>NZ_LN831776.1|WP_046505282.1|6020850_6021450_-|hypothetical-protein
MGSLIYVAAIIIIAIISSLNKAGKNKGGAAPRGGMPTFGGGGGYPLNPGRRAKREPEYGDTNKRSGFPAPGGSTPYPGQPAASCAEADYDASPAWPESSERPSPDYETGEGLSLEQAGEEDGVQARAERMQRELERLHLHFDGAAAGADSGEKGARPDSSPAGSREFAADRNALREGLIWAEILGPPRSRQPRSNRRQI
>NZ_LN831776.1|WP_167330827.1|6021466_6022465_-|flotillin-like-protein-FloA
MEASTITILLIAVVVIIVLSVFFSFFPVMLWVSAWAAGVRISIITLVAMRLRRVTPSRIVNPLIKATKAGLGVNINQLESHYLAGGNVDRVVNALIAAQRADIPLEFTRAAAIDLAGRDVLLAVQMSVNPRVIETPIVAAVAKNGIEVKVKARVTVRANIDRLVGGAGEETIIARVGEGIVTTVGSSSTHKDVLENPDSISRTVLSKGLDSGTAFEILSIDIADVDVGKNIGAYLQTEQAEADKRIAQAKAEERRAMAVAHEQEMKARVVEMKALVVESESQVPLAMAEALRSGKLGVMDYMNLKNIEADTQMRGSLGKLNDGDDSSRPTNK
>NZ_LN831776.1|WP_085981507.1|6022507_6023842_-|nodulation-protein-NfeD
MLFLLPMAGRVSADNTAPRAPGTGPAEPKSGPVFIIPVDQEIERGLQSFLARGFQEAANYGAVLILLEIDTPGGLVSSAEQIGMMVRDSTIPTAAFINGDAASAGSYIALNAGSIIMKPGSMIGAASLVDGKGGSVDDAKLVSYWKAKMVGAAELNGRDPEIAAGMMDKNIVVNKPELGVNKAHGQIIALSSDEALKAGYADSIASTPEEAITSLGYSTDDIFRVEHTGAEKMSHFLTNPIVMTILLFVGIAGIVIEMLVPGFGVPGIIGTLAFALYFFGNYVAGFAGSETWLLFILGLVMLVLELFVPSFGILGLLGSVFLVAGVVRAAYNYTHALFSLGIAFAAAAVVIAIVAVTFKERGIWNRFILQDSLTKEQGFVPVLEKLSLVGASGISITPLRPAGTASLNGERVDVVTEGSFIAAGASISVIKVEGGRVVVKEAAE
>NZ_LN831776.1|WP_020426367.1|6024141_6024585_-|GatB/YqeY-domain-containing-protein
MNLSERLNEDMKQAMKSKDKFTLSTIRMVRSTIKYLEIDLKRTLDDNEVLDILSREIKQRKDALQEFESAGRDELAASTKAEIEIIMKYLPDQLSEEEIKVIVQQTIQETGASSKSEMGKVMSALMPKVKGRADGKLVNQAVLQFLQ

Crispr_ID: NZ_LN831776_62

• CRISPR_ID: NZ_LN831776_62
• CRISPR_location: 6127648-6127722
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_62

Consensus_repeat	Method
AAGTGGAAAAAGGGACACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_62

>62.1|6127671|29|NZ_LN831776|CRISPRCasFinder
TGCCGGAGTACCCTGCCCTCGGGCAGATG

CRISPR arrays and Neighbor proteins around NZ_LN831776_62

CRISPR arrays

The CRISPR arrays of NZ_LN831776_62

>merge|NZ_LN831776|62|6127648-6127722|CRISPRCasFinder
AAGTGGAAAAAGGGACACTAATTTGCCGGAGTACCCTGCCCTCGGGCAGATGAAGTGGAAAAAGGGACACTAATT

>NZ_LN831776|62|62|6127648-6127722|CRISPRCasFinder
AAGTGGAAAAAGGGACACTAATT	TGCCGGAGTACCCTGCCCTCGGGCAGATG
AAGTGGAAAAAGGGACACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020428076.1|6123549_6124071_-|hypothetical-protein	unknown	unknown	gnl|CDD|226398
NZ_LN831776.1|WP_046505377.1|6146870_6149057_-|AAA-family-ATPase	unknown	unknown	gnl|CDD|226482
NZ_LN831776.1|WP_020428075.1|6124173_6125319_-|cysteine-desulfurase	unknown	unknown	gnl|CDD|224029
NZ_LN831776.1|WP_020428077.1|6123325_6123535_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020428081.1|6119348_6120206_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_167345667.1|6132306_6133428_+|tRNA-2-thiouridine(34)-synthase-MnmA	unknown	unknown	gnl|CDD|234664
NZ_LN831776.1|WP_063822379.1|6136584_6139320_-|endoglucanase	unknown	unknown	gnl|CDD|177979
NZ_LN831776.1|WP_020427770.1|6131583_6132003_-|Rrf2-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224870
NZ_LN831776.1|WP_020428080.1|6120202_6121183_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_046505381.1|6149210_6150512_-|NCS2-family-permease	unknown	unknown	gnl|CDD|225161
NZ_LN831776.1|WP_020428074.1|6125516_6125996_-|DUF523-domain-containing-protein	unknown	unknown	gnl|CDD|377367
NZ_LN831776.1|WP_020428073.1|6126081_6126765_+|SOS-response-associated-peptidase	unknown	unknown	gnl|CDD|376837
NZ_LN831776.1|WP_046505366.1|6127093_6127387_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427766.1|6140049_6141354_-|replication-associated-recombination-protein-A	unknown	unknown	gnl|CDD|237355
NZ_LN831776.1|WP_081487171.1|6121257_6122703_-|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270450
NZ_LN831776.1|WP_020428078.1|6122779_6123082_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046505370.1|6142259_6144278_+|methyl-accepting-chemotaxis-protein	unknown	unknown	gnl|CDD|223910
NZ_LN831776.1|WP_082118191.1|6145371_6146655_+|IS4-family-transposase	unknown	unknown	gnl|CDD|280446
NZ_LN831776.1|WP_020427765.1|6141480_6141762_-|hypothetical-protein	unknown	unknown	gnl|CDD|337191
NZ_LN831776.1|WP_082118145.1|6133575_6136557_-|cellulose-1,4-beta-cellobiosidase	unknown	unknown	gnl|CDD|376714

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020428076.1|6123549_6124071_-|hypothetical-protein	gnl|CDD|226398	COG3881, COG3881, PRC-barrel domain containing protein [General function prediction only].	1.24365e-24
NZ_LN831776.1|WP_046505377.1|6146870_6149057_-|AAA-family-ATPase	gnl|CDD|226482	COG3973, COG3973, Superfamily I DNA and RNA helicases [General function prediction only].	1.14691e-117
NZ_LN831776.1|WP_020428075.1|6124173_6125319_-|cysteine-desulfurase	gnl|CDD|224029	COG1104, NifS, Cysteine sulfinate desulfinase/cysteine desulfurase and related enzymes [Amino acid transport and metabolism].	0
NZ_LN831776.1|WP_063822379.1|6136584_6139320_-|endoglucanase	gnl|CDD|177979	PLN02345, PLN02345, endoglucanase.	1.47226e-134
NZ_LN831776.1|WP_020428081.1|6119348_6120206_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.37708e-79
NZ_LN831776.1|WP_167345667.1|6132306_6133428_+|tRNA-2-thiouridine(34)-synthase-MnmA	gnl|CDD|234664	PRK00143, mnmA, tRNA-specific 2-thiouridylase MnmA; Reviewed.	0
NZ_LN831776.1|WP_020427766.1|6140049_6141354_-|replication-associated-recombination-protein-A	gnl|CDD|237355	PRK13342, PRK13342, recombination factor protein RarA; Reviewed.	0
NZ_LN831776.1|WP_020427770.1|6131583_6132003_-|Rrf2-family-transcriptional-regulator	gnl|CDD|224870	COG1959, COG1959, Predicted transcriptional regulator [Transcription].	1.90974e-49
NZ_LN831776.1|WP_020428080.1|6120202_6121183_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	2.24702e-66
NZ_LN831776.1|WP_046505381.1|6149210_6150512_-|NCS2-family-permease	gnl|CDD|225161	COG2252, COG2252, Xanthine/uracil/vitamin C permease [Nucleotide transport and metabolism].	2.0291e-109
NZ_LN831776.1|WP_020428074.1|6125516_6125996_-|DUF523-domain-containing-protein	gnl|CDD|377367	pfam04463, DUF523, Protein of unknown function (DUF523). Family of uncharacterized bacterial proteins.	1.18403e-58
NZ_LN831776.1|WP_020428073.1|6126081_6126765_+|SOS-response-associated-peptidase	gnl|CDD|376837	pfam02586, SRAP, SOS response associated peptidase (SRAP). The SRAP family functions as a DNA-associated autoproteolytic switch that recruits diverse repair enzymes onto DNA damage. We propose that the human protein Q96FZ2:UniProtKB, the eukaryotic member of the SRAP family, which has been recently shown to bind specifically to DNA with 5-hydroxymethylcytosine, 5-formylcytosine and 5-carboxycytosine, is a sensor for these oxidized bases generated by the TET (tetrahedral aminopeptidase of the M42 family) enzymes from methylcytosine. Hence, its autoproteolytic activity might help it act as a switch that recruits DNA repair enzymes to remove these oxidized methylcytosine species as part of the DNA demethylation pathway downstream of the TET enzymes.	3.09353e-109
NZ_LN831776.1|WP_081487171.1|6121257_6122703_-|sugar-ABC-transporter-substrate-binding-protein	gnl|CDD|270450	cd14747, PBP2_MalE, Maltose-binding protein MalE; possesses type 2 periplasmic binding fold. This group includes the periplasmic maltose-binding component of an ABC transport system from the phytopathogen Xanthomonas citri and its related bacterial proteins. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.2769e-134
NZ_LN831776.1|WP_046505370.1|6142259_6144278_+|methyl-accepting-chemotaxis-protein	gnl|CDD|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	2.30415e-57
NZ_LN831776.1|WP_082118191.1|6145371_6146655_+|IS4-family-transposase	gnl|CDD|280446	pfam02281, Dimer_Tnp_Tn5, Transposase Tn5 dimerization domain. Transposons are mobile DNA sequences capable of replication and insertion into the chromosome. Typically transposons code for the transposase enzyme, which catalyzes insertion, found between terminal inverted repeats. Tn5 has a unique method of self- regulation in which a truncated version of the transposase enzyme acts as an inhibitor. The catalytic domain of the Tn5 transposon is found in pfam01609. This domain mediates dimerization in the known structure.	9.85871e-18
NZ_LN831776.1|WP_020427765.1|6141480_6141762_-|hypothetical-protein	gnl|CDD|337191	pfam08765, Mor, Mor transcription activator family. Mor (Middle operon regulator) is a sequence specific DNA binding protein. It mediates transcription activation through its interactions with the C-terminal domains of the alpha and sigma subunits of bacterial RNA polymerase. The N terminal region of Mor is the dimerization region, and the C terminal contains a helix-turn-helix motif which binds DNA.	5.60721e-05
NZ_LN831776.1|WP_082118145.1|6133575_6136557_-|cellulose-1,4-beta-cellobiosidase	gnl|CDD|376714	pfam02011, Glyco_hydro_48, Glycosyl hydrolase family 48. Members of this family are endoglucanase EC:3.2.1.4 and exoglucanase EC:3.2.1.91 enzymes that cleave cellulose or related substrate.	0

Protein sequences

>NZ_LN831776.1|WP_046505366.1|6127093_6127387_+|hypothetical-protein
MDTNYQQVSWSCMNKYVGIITTDGQSHDGFIAHVDQDYVTLAIPTNEMMGHMNGMPAQASTYRQFGFFPGFFPRRRFFPRRIPFGSVASLFLLPFFI
>NZ_LN831776.1|WP_020428073.1|6126081_6126765_+|SOS-response-associated-peptidase
MCGRYTITVSMEELMLWYLIEDTTIVHYAPKYNAAPMQSIPAVIHDGKQNRLGKLRWGLVPSWAKEDKIGSKMINARSESLQDKPAFRNLISTRRCIIPADGFYEWKQQNGRKQPMRITLKSGELFSMAGLYDIWMDASGNRLSTCTIITTGANSLMADIHDRMPVILSREAESEWLDRNNRQVPDLMKLLQPYSADQMRAYPVSSAVGTVRNDAKELVDEVKESAG
>NZ_LN831776.1|WP_020428074.1|6125516_6125996_-|DUF523-domain-containing-protein
MIIVSSCLAGMKVRYNSTDCLDETIHQLLDNNRAVAVCPELLGEFSTPREPAEIVGGDGGAVLDGTAKVMDRLGNDVSEMYILGAYKALEQARNAGASIVVLKENSPSCGSSMIYNGAFAGQKIPGEGVTAALLRRNGIEVISEEQLPARLGELGALDK
>NZ_LN831776.1|WP_020428075.1|6124173_6125319_-|cysteine-desulfurase
MKPIYLDHAASTPVHPEVAKVMYNMLLEQFGNASSVHTYGRSAKKMINSARDTIAGFLGCAPDEWVFTSGGTESDNLALFGAASASAHKGKHIITTAVEHHAVLHTCEALEKQGFSVTYLPVNTEGRVSAADVEAALREDTVLISVMFANNEVGTVEPIQEIGRLAAERGILFHVDAVQVLGLLSIALRELPVDYMSFTAHKINGPQGIGGLYVRRGAPLQPRQHGGLQERGRRAGTESLAGAAGFAKAVELAVTGLEQRREKALTLRTVLLQELDRRIGRESYVINGDKQHFLPGILNLSFPGVSTDVMLMNLDMEGIAAASGSACTSGSLEISHVLRAMKLPDELLNSAIRFSTGMGNTNEEMEYVAQKVETILKRLRK
>NZ_LN831776.1|WP_020428076.1|6123549_6124071_-|hypothetical-protein
MKLQEMIGLAVYEVEEGNEIGKIVDILLDSNWNITGIELESKAFFSSHVKVVAWEDIVAYGEDAVMIRSKESIVKADTDHIPYTFLLGKKKLKDLQVLTASGTILGRVSDVYFDQKLGNTIVALEISDGLVTDLIEGRKWLPCSEGMSIGENSVLVPAMSEERLQKAINIVNG
>NZ_LN831776.1|WP_020428077.1|6123325_6123535_-|hypothetical-protein
MKCPNCNSKDIGKIGSHQFYCWGCFIELTVNGEKMSVYQVEEDGTLSSLDDLFSGEEIAQDYPQIHASS
>NZ_LN831776.1|WP_020428078.1|6122779_6123082_-|hypothetical-protein
MRLCCCQGFSFRKHGTGTSSSGDGRVSRISRKRRRHYCSRNGSVCTDYAVYTLEFDVTGGSTSIGRISFELGNIADGGTGQLAVDVDDIVLTNNGTVSVP
>NZ_LN831776.1|WP_081487171.1|6121257_6122703_-|sugar-ABC-transporter-substrate-binding-protein
MEDGRPFSEIFKRQWGRFIVKKTAVSISALLLAFSVAVSGCGGSNNSANNGEKKENSSATTASAAPSTEPVTLNAWVMPNSPKPDADFMKTLDPYLKEHPNVTVKVTVLDWGSAWTKITTAATSGEGPDLLQLGSTWVPAIASMGGIDKVTDKVADVGGAEAFLPAIWKTTSIAGDSEVYGVPWFVDARAIYYRTDVFKQAGVNPETAFKDWDSFKSALEAVNGQTVDGKKIAALGLPGKNDWNVVHNIFPWIWAAGGDVLSEDNKNVIFNEEKGLKGVMFYTGLAHEGLVDKSSLEKNSSQIESDFGDGKSAVIISGPWLAKNFATPKANGGMDDKKAAKNFAVAPLPAGPGGQSTFVGGSELTVFSGSKNKEATWELIKYLTSDEAQKTYANVSGQLPTKLSILDAPDLDANMKAFSEATKYGKTYPSIPQWGPTETALQKHFANIWDIVAGVKGKYSEESVKQELDSAASEVKAIINQ
>NZ_LN831776.1|WP_020428080.1|6120202_6121183_-|sugar-ABC-transporter-permease
MGLHTENNLPAKAPSRKRGLWRKRVRDNKFAYMLMVPTIIFMMLVHLLPMLQGIWMSFLKLNQFTLVKYLKAPFVGLDNYVGLLFNSDNPVRQGLNFAIRNTAIYAVIVTIGVMIMGLMMAMLLNRDFPGRGIARTAMLLPWVVPSYVVGVLWGFMWQQNGIINYILVDVLHLFAEKPFWLLGTNTIWAIIIPTIWRGWPFLMVIFLAGLQTIPDDIYEAATIDGAGKFRQFWNMTLPMLKPVIAVQLLFQIINNVYSYNIVSTMFGNGAGYPGEWGDLLMTALTRQSFGYWSFGSGSAASMMLMVVMLMVVGVWYRAFRTELNAQ
>NZ_LN831776.1|WP_020428081.1|6119348_6120206_-|carbohydrate-ABC-transporter-permease
MSIHRKRSVTSFLLTSLTWFIVVVTIFPILWMIFTSLHSNDQILNGITTFSLPKPQWVNYVNMWDTVNFAIYFRNSLLICGATTLLAGAFAVLAGYALARFDFPGSKLFSMSIISTQLIPGIMFLFPIYLMFLWIKNTFGLPMINTYWGMILVYTAFYTPISIWIMRGFFVSIPRDLEESAVIDGCSKFQAFYKIILPLSVPGIIATGIFIFLTAWDELLFAWVLTTSSDVQTIPVGIRLFVGQYNTRYDLLMAASTVVTVPVMVIFFMTQKYFISGMTAGAVKG
>NZ_LN831776.1|WP_020427770.1|6131583_6132003_-|Rrf2-family-transcriptional-regulator
MKISTKGRYGLTIMMELALKFGEGPTSLKSIAEKNGLSEHYLEQLIAPLRNAGLVKSIRGAYGGYILSREAGTITAGDIIRVLEGPISPVDFTEEDDPAKRDLWLRIRDSIADVLDSTTLSDLINFKEESHADNYMFYI
>NZ_LN831776.1|WP_167345667.1|6132306_6133428_+|tRNA-2-thiouridine(34)-synthase-MnmA
MTKANQDTRVVVGMSGGVDSSVTALLLKQQGYDVIGIFMKNWDDTDEFGVCTAETDAEDVRRVCEQIDIPYYTVNFEKEYFDKVFSYFLDEYKAGRTPNPDVMCNREIKFGEFLNKALQLGADYVATGHYARVIEEDDVFKLLRGVDSNKDQTYFLNALNQYQLSKAMFPIGHLPKPEVRRIAEEAGLYTAKKKDSTGVCFIGERNFREFLSQYLPAQSGDMVDIATGEVKGRHEGLMYYTLGQRQGLGIGGSGTGEPWFVAEKDLNRNILYVVQGDKHPSLYSTSLTASGVNWIEEGTLGTAPLKCTAKFRYRQPDQGVTLTAQEDGTVHVAFDVPQKAITPGQAVVFYLGEQCLGGGTIEAAEKVVPLPQL
>NZ_LN831776.1|WP_082118145.1|6133575_6136557_-|cellulose-1,4-beta-cellobiosidase
MKKLSSIKKPISLAMAAVLTLTLVTGIFNFRPATAQAASVEQTRFLQMYSQLKDPANGYFSAEGVPYHSVETLLSEAPNYGHMTTSEAYSYWMWLEVLYGYHTGDWSKLESAWDNMEKYIIPVNEGDGVQEQPTMSYYNPNSPATYASEFGQPDQYPSPLNGKYSPGKDPLDAELKSAYGNNQTYLMHWLVDVDNWYGFGNLLNPAHTAAYVNTFQRGTQESVWEAVPHPSQDDKSFGKTNEGFMSLFTKESNVPAAQWRYTDATDADARAVQAMYWAKELGYNNTVYLNKAKKMGDYLRYGMYDKYFQKIGSAADGTPEAGTGKDASHYLLAWYTAWGGGLGASGNWAWRIGASHAHQGYQNVVTAYALSDPAGGLVPASATAGQDWSKSLTRQLEFYNWLQSSEGAIAGGATNSYNGSYSAYPAGTSTFYGMAYDEAPVYTDPPSNNWFGMQAWSVERVAELYYILASGGDTTSANFQMAKRVIENWIDWSTDYAFAGSRPLADAEGYYLNKQGQRILGGDDPEVATVSAPGEFWIPGNVEWQGQPDTWTGFSTFSGNSNLKAVTKNPGQDTGVLGSYIKALTFFAAGNKAEHGSYTALGGTASQLAKSLLDTAWGYNDGVGITTVEKRGDYSRYFTKEVYFPAGWTGTFGQGNTIPGSTTVPSDPAKGGNGVYASYTDVLPAIKNDPKWSYLQGKYNSSYNQATRTWDSGAPEFTYHRFWSQVDMATAYAEYDRLINTPTEEPAAPKAPSKPAAAAGDKVVALSWNKVRGADSYTVKRATISGGPYTALGNVTQATYSDTRVVNDTTYYYVVSATNTAGTSPDSPEVSAKPTAVPIPTVGDLVVQYRTTDTNPGDSQLRPQLRIVNNGTTAVELSKLKLRYYYTVDGDKAQQFNVDYATVGSGNVLGSFVKLVPAATGADYYVEISFSPAAGSLAPGANTGEIQLRINKTDWSNYNETGDYSYNPAKTAYTDWSRVPLYLNGVLVWGLQP
>NZ_LN831776.1|WP_063822379.1|6136584_6139320_-|endoglucanase
MSPRKRKQGLILSLSVMLTCTMFSGAVFHPSVAKAEGSGYNYAEALQKSIYFYETQRSGELPDNNRVEWRGDSGLQDGADVGHDLTGGWYDAGDHVKFGFPMAYTATMLAWSVYEYKEGYVQSGQLDEILDNIRWATDYFMKAHTAPNELWGQVGNGTADHNWWGAAEVMPMARPSYKIDAAHPGSDLAAETAAALASAAIIFRDSDAAYADKLLLHAKQLYNFADTYRGVYSESITDATQYYKSWSGYADELSWGGVWLYMATGDQTYLDKAVTASNSWSTNQSGQWGYQWTQSWDDKHYGAQLLLSRITDDPKFIQSTERNMQFWTTGVNGTTDRVAYTPGGLAHLDQWGALRYAATQAFLAFVYADWVGDPVKQNTARTFAERQITYMLGDNPRSSSYVIGFGSNALQHPHHRTSHGSWSDSQTTPANHRHVLYGALVGGPSKTDSYTDTISDYVSNEVATDYNSAFTGALAKMMLLHGQGQQPLENFPPAETREDEMFTETSVNASGSNFVEIRALLNNRSGWPARSSSQMSFYYYVDLSEAAAAGYGPEDITVKAGGYNQGGTVSQLLPFDEANHIYYTKIDFTGTPVYPGGQSAYRKEIQFRISAPLNTAFWDNTNDFSFKGVASGASSPVKNPYIPVFDAGVKVYGELPSGGNPGEPQVPGRPSGLQATAGNASVSLAWNAVSGATGYTIKRSLVNGGPYAAIGTVTGTTYSDSGLVNGVDYYYVVTASNSVGEGTASAQAAARPRETTPPAKGDLRVQYRTNDTSPGDAQIRSQFRIVNTGKEAVALSGLKLRYYYTVDGDKPQEFHCDYAVLGSGNLSGSFVKLAAPAALADSYVEISFAPGAGNLAPGADTGEIQVRINKTDWTPYNESNDYSYSGTQQAFADWDKVTLHREGTLVWGLEP
>NZ_LN831776.1|WP_020427766.1|6140049_6141354_-|replication-associated-recombination-protein-A
MDLFSFGEDTAGGRLLADRMRPENLDEYIGQEHIVGPGKLLRRAIEADQVSSILLYGPPGCGKTTLAHIISHHTQGEFVRLNAVEASVKDVREVIERAQSNKSLYGSKTILFLDEVHRFNSSRQDALLPAVEKGTIIFIGATTENPFHYVNGALMSRSTLFQLESLTSEHSLVAMRRALADEKRGLGFMQLQADEEALQHIADMANGDIRRALNALELAAMTTAPEPDGSVHITLAVAEESIRRPIVKADESTQYDVLSAFHKSIRGSSDAALFWFLYAVEKLGMDPMTFIRRLIAASSEDIGLANPQAMVQAVSALEAYRNNGWPEAKLNIAQAILFAVESPKSNAVVMAISRAMDSIEELKSAEVPLHLRDTHYKGSAALGHEGYQYPHNFPGHYVKQEYLPKAISRREFYQATEQGNEAKIRHNQGLRRGQ
>NZ_LN831776.1|WP_020427765.1|6141480_6141762_-|hypothetical-protein
MSYVNGKDVLPPGLLEELQGYIQGELLYIPKKTEQRVKWGENSGSRQEIASRNEEIFCSHSSGCSVNELQKRYHLSEESIRKIISKMRLAMNR
>NZ_LN831776.1|WP_046505370.1|6142259_6144278_+|methyl-accepting-chemotaxis-protein
MSAVRSALTRFFHIKKLRTELMLFIITAIVIPSLALAVISSETSKTELRSKMEDTTNSSIHILDKTLTQLIQLESASVNELADQISAADVTSGSARVRKLIDKFKAEHPEIDIVSLGNTDGKFMLSPTSDQKDYDPRVRDWYIDALKFPESASVIDPIFSKVTGSYIMPISRAFPDGKGAISVSLSMNGLMELAKTVSLGSSGYAYILDSQNKVIYHPAMEVATPVTGALLDALSAAPMGKVSYKDTTADMQMAGYYVTNELSGFKIVGVLPADEYTRAVYPILYKSAIVLAVALIVAIAVTFLIIRRITAPLEALNRSAKRVSEGQLDESVTTRRKDEIGELAGNYNAMVQSLRTMVQDVSETSGHLAAASEQLTASTGENSKAVEYVTELIEDSTRGVEAQASASAEVATTMDEMSEAIHKIASASQSIVSAALLTEKDVNNGSAKVQHVGNQMQTIHHSVQQSSRLIADLNGLSAKVAETSTAIASIAKQTNLLSLNAGIEAARAGEHGRGFAVVAGEVRKLSEASKVSAGEIQETISEMVGLIASVYDVMRHQVVADVEQGMTLALEAGEAFTQIEQSTRHVGEQIHEVSAITEQMSASSAEVAASVQEMANIAKAALDSFQSVTAATEEQLASMEEITSSSAALSAMASDMQQQVERFQFTAQHEGQ
>NZ_LN831776.1|WP_082118191.1|6145371_6146655_+|IS4-family-transposase
MTTLSTRLGSSISAASADNAERQAIGRLLKNAAITEENVLDCYRLETIRQMKETGEQVFLCVQDTTGVSYGQRDKTTGLGQYTTSNTKGLLTHSAVVFTTTGLPLGLLYQKIWAREPQAKGKRKVSRPYEEKENYRWTEAAQVSAAAVPASLKLIHIGDREADFFEFLVQLQQDGQSYVVRSMQNRITEDGGERLWDKVRAQPAAGEIRVSLPRDTRRGTPARETTLALRFTSSTVQVPIHLQQKGADYSPLSCTLIHVVEVTPLEDQAPIEWFLVTNVSTTNADEAAEKVAWYVQRWKIERFHYILKNGCEVEKLQEHQANRLQKLILFYSIIALQIQHLTYRSREQPEAPATEVIREDEWQVLYRIAYRTKTVPQQPATLKEVVFALAKLGGFLGRKSDGDPGAKVIWRGLRRFRDVYESYHYLM
>NZ_LN831776.1|WP_046505377.1|6146870_6149057_-|AAA-family-ATPase
MEDNFQSAYQEEEDRLNSALTEIDTVLERLRGIPVYTGHDYTEQALEVSREQRRKDLAKLRQEPYFGRLDFQGKDEDGRKALYIGKIGVDREQVSDRPLVIDWRAPVASLFYSFTGGTEPASYEAPEGLIEGLVYLKRNVVIRKQILERVADTYNRDSDGPAVSDEFLVYRLGENKDNRLRDIVSTIQEEQDKIIRAAKNTALIIQGVAGSGKTTVALHRLAFLLYQYKEQVSAEKMIIFAPNRMFLDYISDVLPELGVGNIAQSTFPDWAADVLGVVLPEQNAAETMSYWFEREGGMPEITEETPGRFKGSTALMGIIESVIGLLENGAVPAGDFSPWEGSVLHRSMILRWHNEEYAPYPPAKRKERVMARIHRWIEMELKKSPSAAAMKDRKKKSAAREKAYSAKWPKYDPLTIYKQIFRAVKVPEDWPAEAPESIPPEVLASTVKELKKGILHEEDLPPLLYIHYLLNGNEGGSGFDHIVIDEAQDFSPFQIAVLDLYVKGHSFTILGDLSQGIHAYKGVHAWEEMQTLFAPEHTAYHALTRSYRSTMEIIEFANGILSAGVGSSLLAVPVFRSGNPVRLISYGQPLPASAAGGDRRIQAVRTALASLSGREYRTLAVLTRSLREAAELYTELAGHFEDIHLIDGSMTEYRGGLSVLPVYLSKGLEFDAVILADADSDHYGGAAWDAKLMYVGCTRALHELWILHGEGLPPYLQNGEGTVQGWPE
>NZ_LN831776.1|WP_046505381.1|6149210_6150512_-|NCS2-family-permease
MNSKVWRNRVGLEPGDNWKRELSAGILSYFASVYIVMVNAAILHDAGMPLRAGMVATLLTAVAGCLLMAFGGKTPIVVVPGMGINAFFTYTLVHSMKLDWREALAVVAVTGVLFAIVAFTSLYRILSDAIPHNLQHAITVGIGLFLTFIGLQKSGIVIAHRTTFVAIGHFSDPAVITSCVTLILALVLFIRGTRGGLLISMLAGTGMAYLLGAAHVPENTDSGHMFAGYSGVFAGMDWGRGLSLVFWIAVFLLLLIVVFENIGLISSQTLMAGRPERFKSSLRALSIANIAAGLFGSSPVVAAAESTAGIAAGGRSGLTSLITGLLFGATFLFIPLLAYVPDSAIAPILIVIGGLMVQNVREMDLSDLTELFPAFLIMVMIPFTYSIVDGMAFGFITYPVVKLAMGKGKEVPPALYGIAGLFIANFVLHAFMG

Crispr_ID: NZ_LN831776_63

• CRISPR_ID: NZ_LN831776_63
• CRISPR_location: 6226982-6227056
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_63

Consensus_repeat	Method
AAGTGGAAAAAGGTACACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_63

>63.1|6227005|29|NZ_LN831776|CRISPRCasFinder
TGCCGAAGTACCCTACCCTCGGGCAGATA

CRISPR arrays and Neighbor proteins around NZ_LN831776_63

CRISPR arrays

The CRISPR arrays of NZ_LN831776_63

>merge|NZ_LN831776|63|6226982-6227056|CRISPRCasFinder
AAGTGGAAAAAGGTACACTAATTTGCCGAAGTACCCTACCCTCGGGCAGATAAAGTGGAAAAAGGGACACTAATT

>NZ_LN831776|63|63|6226982-6227056|CRISPRCasFinder
AAGTGGAAAAAGGTACACTAATT	TGCCGAAGTACCCTACCCTCGGGCAGATA
AAGTGGAAAAAGGGACACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020429278.1|6245105_6246416_-|GTPase-ObgE	unknown	unknown	gnl|CDD|237046
NZ_LN831776.1|WP_020429276.1|6243743_6244916_-|SPFH-domain-containing-protein	unknown	unknown	gnl|CDD|259806
NZ_LN831776.1|WP_020429270.1|6240133_6241420_-|homoserine-dehydrogenase	unknown	unknown	gnl|CDD|235783
NZ_LN831776.1|WP_039786108.1|6218963_6219044_-|K(+)-transporting-ATPase-subunit-F	unknown	unknown	gnl|CDD|378219
NZ_LN831776.1|WP_020426649.1|6225871_6226819_+|phosphoglycerate-dehydrogenase	unknown	unknown	gnl|CDD|240650
NZ_LN831776.1|WP_020426641.1|6215212_6217240_-|potassium-transporting-ATPase-subunit-KdpB	unknown	unknown	gnl|CDD|234905
NZ_LN831776.1|WP_020426640.1|6214623_6215196_-|potassium-transporting-ATPase-subunit-KdpC	unknown	unknown	gnl|CDD|376890
NZ_LN831776.1|WP_039786114.1|6217263_6218931_-|potassium-transporting-ATPase-subunit-A	unknown	unknown	gnl|CDD|377138
NZ_LN831776.1|WP_020429273.1|6242220_6242970_-|hypothetical-protein	unknown	unknown	gnl|CDD|379090
NZ_LN831776.1|WP_020429274.1|6242984_6243731_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020429266.1|6238212_6239100_-|prephenate-dehydratase	unknown	unknown	gnl|CDD|237013
NZ_LN831776.1|WP_020427265.1|6228677_6229277_-|AAA-family-ATPase	unknown	unknown	gnl|CDD|379082
NZ_LN831776.1|WP_020426647.1|6223374_6224634_-|hypothetical-protein	unknown	unknown	gnl|CDD|341491
NZ_LN831776.1|WP_020426645.1|6219706_6220414_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_LN831776.1|WP_020429271.1|6241562_6242000_-|ACT-domain-containing-protein	unknown	unknown	gnl|CDD|179848
NZ_LN831776.1|WP_020426646.1|6220406_6223106_-|sensor-histidine-kinase-KdpD	unknown	unknown	gnl|CDD|225115
NZ_LN831776.1|WP_046505430.1|6224806_6225691_-|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223656
NZ_LN831776.1|WP_020426644.1|6219174_6219504_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020429268.1|6239096_6240077_-|homoserine-kinase	unknown	unknown	gnl|CDD|234920
NZ_LN831776.1|WP_020429264.1|6237326_6238208_-|branched-chain-amino-acid-transaminase	unknown	unknown	gnl|CDD|236238

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020429278.1|6245105_6246416_-|GTPase-ObgE	gnl|CDD|237046	PRK12297, obgE, GTPase CgtA; Reviewed.	0
NZ_LN831776.1|WP_020429276.1|6243743_6244916_-|SPFH-domain-containing-protein	gnl|CDD|259806	cd03408, SPFH_like_u1, Uncharacterized family; SPFH (stomatin, prohibitin, flotillin, and HflK/C) superfamily. This model summarizes an uncharacterized family of proteins similar to stomatin, prohibitin, flotillin, HflK/C (SPFH) and podocin. The conserved domain common to the SPFH superfamily has also been referred to as the Band 7 domain. Many superfamily members are associated with lipid rafts. Individual proteins of the SPFH superfamily may cluster to form membrane microdomains which may in turn recruit multiprotein complexes. Microdomains formed from flotillin proteins may in addition be dynamic units with their own regulatory functions. Flotillins have been implicated in signal transduction, vesicle trafficking, cytoskeleton rearrangement and are known to interact with a variety of proteins. Stomatin interacts with and regulates members of the degenerin/epithelia Na+ channel family in mechanosensory cells of Caenorhabditis elegans and vertebrate neurons and participates in trafficking of Glut1 glucose transporters. Prohibitin may act as a chaperone for the stabilization of mitochondrial proteins. Prokaryotic HflK/C plays a role in the decision between lysogenic and lytic cycle growth during lambda phage infection. Flotillins have been implicated in the progression of prion disease, in the pathogenesis of neurodegenerative diseases such as Parkinson's and Alzheimer's disease and, in cancer invasion and metastasis. Mutations in the podocin gene give rise to autosomal recessive steroid resistant nephritic syndrome.	1.16646e-88
NZ_LN831776.1|WP_020429270.1|6240133_6241420_-|homoserine-dehydrogenase	gnl|CDD|235783	PRK06349, PRK06349, homoserine dehydrogenase; Provisional.	0
NZ_LN831776.1|WP_039786108.1|6218963_6219044_-|K(+)-transporting-ATPase-subunit-F	gnl|CDD|378219	pfam09604, Potass_KdpF, F subunit of K+-transporting ATPase (Potass_KdpF). This entry describes a very small integral membrane peptide KdpF, a subunit of the K(+)-translocating Kdp complex. It is found upstream of the KdpA subunit (IPR004623). Because of its very small size and highly hydrophobic character, it is sometimes missed in genome annotation.	0.000504723
NZ_LN831776.1|WP_020426649.1|6225871_6226819_+|phosphoglycerate-dehydrogenase	gnl|CDD|240650	cd12173, PGDH_4, Phosphoglycerate dehydrogenases, NAD-binding and catalytic domains. Phosphoglycerate dehydrogenases (PGDHs) catalyze the initial step in the biosynthesis of L-serine from D-3-phosphoglycerate. PGDHs come in 3 distinct structural forms, with this first group being related to 2-hydroxy acid dehydrogenases, sharing structural similarity to formate and glycerate dehydrogenases. PGDH in E. coli and Mycobacterium tuberculosis form tetramers, with subunits containing a Rossmann-fold NAD binding domain. Formate/glycerate and related dehydrogenases of the D-specific 2-hydroxyacid dehydrogenase superfamily include groups such as formate dehydrogenase, glycerate dehydrogenase, L-alanine dehydrogenase, and S-adenosylhomocysteine hydrolase. Despite often low sequence identity, these proteins typically have a characteristic arrangement of 2 similar subdomains of the alpha/beta Rossmann fold NAD+ binding form. The NAD+ binding domain is inserted within the linear sequence of the mostly N-terminal catalytic domain, which has a similar domain structure to the internal NAD binding domain. Structurally, these domains are connected by extended alpha helices and create a cleft in which NAD is bound, primarily to the C-terminal portion of the 2nd (internal) domain. Some related proteins have similar structural subdomain but with a tandem arrangement of the catalytic and NAD-binding subdomains in the linear sequence.	4.30954e-103
NZ_LN831776.1|WP_020426647.1|6223374_6224634_-|hypothetical-protein	gnl|CDD|341491	cd17792, CtkA, serine/threonine-protein kinase CtkA and similar proteins. The Helicobacter pylori serine/threonine-protein kinase CtkA (proinflammatory kinase), encoded by the jhp940 gene, has been shown to be secreted by the bacterium and to induce cytokines in gastric epithelial cells. It may play a role in chronic gastric inflammation. CtkA autophosphorylates itself at a threonine residue near the N-terminus and it translocates into cultured human cells. It also enhances phosphorylation of the NF-kappaB p65 subunit at Ser276 in human epithelial cancer cells; phosphorylation at this position is known to activate the transcriptional activity of NF-kappaB.	3.5452e-12
NZ_LN831776.1|WP_020426640.1|6214623_6215196_-|potassium-transporting-ATPase-subunit-KdpC	gnl|CDD|376890	pfam02669, KdpC, K+-transporting ATPase, c chain. This family consists of K+-transporting ATPase, c chain, KdpC. KdpC forms strong interactions with the KdpA subunit, serving to assemble and stabilize the Kdp complex. It has been suggested that KdpC could be one of the connecting links between the energy providing subunit KdpB and the K+-transporting subunit KdpA. The K+ transport system actively transports K+ ions via ATP hydrolysis.	2.09319e-90
NZ_LN831776.1|WP_039786114.1|6217263_6218931_-|potassium-transporting-ATPase-subunit-A	gnl|CDD|377138	pfam03814, KdpA, Potassium-transporting ATPase A subunit.	0
NZ_LN831776.1|WP_020429273.1|6242220_6242970_-|hypothetical-protein	gnl|CDD|379090	pfam13248, zf-ribbon_3, zinc-ribbon domain. This family consists of a single zinc ribbon domain, ie half of a pair as in family DZR. pfam12773.	0.00295309
NZ_LN831776.1|WP_020429266.1|6238212_6239100_-|prephenate-dehydratase	gnl|CDD|237013	PRK11898, PRK11898, prephenate dehydratase; Provisional.	8.727e-109
NZ_LN831776.1|WP_020427265.1|6228677_6229277_-|AAA-family-ATPase	gnl|CDD|379082	pfam13238, AAA_18, AAA domain.	1.07101e-05
NZ_LN831776.1|WP_020426645.1|6219706_6220414_-|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	3.14471e-78
NZ_LN831776.1|WP_020429271.1|6241562_6242000_-|ACT-domain-containing-protein	gnl|CDD|179848	PRK04435, PRK04435, ACT domain-containing protein.	9.4248e-73
NZ_LN831776.1|WP_020426646.1|6220406_6223106_-|sensor-histidine-kinase-KdpD	gnl|CDD|225115	COG2205, KdpD, Osmosensitive K+ channel histidine kinase [Signal transduction mechanisms].	0
NZ_LN831776.1|WP_046505430.1|6224806_6225691_-|LysR-family-transcriptional-regulator	gnl|CDD|223656	COG0583, LysR, Transcriptional regulator [Transcription].	1.14279e-25
NZ_LN831776.1|WP_020426641.1|6215212_6217240_-|potassium-transporting-ATPase-subunit-KdpB	gnl|CDD|234905	PRK01122, PRK01122, potassium-transporting ATPase subunit KdpB.	0
NZ_LN831776.1|WP_020429268.1|6239096_6240077_-|homoserine-kinase	gnl|CDD|234920	PRK01212, PRK01212, homoserine kinase; Provisional.	5.23409e-116
NZ_LN831776.1|WP_020429264.1|6237326_6238208_-|branched-chain-amino-acid-transaminase	gnl|CDD|236238	PRK08320, PRK08320, branched-chain amino acid aminotransferase; Reviewed.	0

Protein sequences

>NZ_LN831776.1|WP_020426649.1|6225871_6226819_+|phosphoglycerate-dehydrogenase
MKILIVGYFNETSKSNIARYFPQDWNVVVVPPGQEMLHHIEDCQVIIPEHIKVDHSLLSIAKKLKLVQTGAGFDNVDVPACTQLGIWVANAAGVNAQAVAEHVMALILSYYKNIPFLDTFMKNKMDESQLDYTGSELKGKTIGIIGLGAIGKKVAAFCRVFDMNVLAYARNAVVQSDGFVKMTDFDTLLSTSDIISVHIPLNQQTKQLINKAVFKKMKNSTLFINTARGGIVNERDLIDALKNGDISGACLDVFESEPLPIDSELRNLGNVILTPHTAGMPDGRKFHKKRYDFFINNIKRIENGEEPESKLNQLL
>NZ_LN831776.1|WP_046505430.1|6224806_6225691_-|LysR-family-transcriptional-regulator
MYFPGIEAFLAIVRTESISKAAELLHLSQATVSYRLKTLEQEMGGLLVERRKGAPKISLTPKGENFFSIAERWEALWRETQILQASGSQLSLAISAAESISHFVLPPVYRMLNQYTPSIRLQIRTQHTQEAFDSIERREMDVAFVVREIVSPSVTVKPFFTEEMVLLRLAVPGRQAGDTVEMEELAAEHEVFINWNREFQFRHDQWWDPLCPSRVHLDTAGLITTFLKDARQWTIVPASIGAHMIRMGDFVLQKLSVSVPPRTCYKVTHKFPNQALHEPLRILDNYLQDIFGIQ
>NZ_LN831776.1|WP_020426647.1|6223374_6224634_-|hypothetical-protein
MADSWNKSYTLMHKNEPVAEIELDEATVSISAIGQVYAKQHVPVGIPVKKGKIDRAGLNEWWRGRAIPASRDGIKEALLELNLSATQKLLDKSYGLSLSDQYWIRPSAPELKWNNINFFGNPFSEDVGNVLFGKVSSDAVSLVSPDNTSDGWLKKKWAIINGKRCLIKGGSGATQQEPYNEVIASKIMERLGIPHVPYTLIEQEDYPYSVCENFITPQTELITAWYVMHTQQKPNHVSVYQHYVSCCEELGIPGIVKALDQMMVVDYLVANEDRHQNNFGVIRHAETLEWIGPAPIFDSGSSLWFSKPLGLIRADGKLTCKPFKPDHNEQIKLVTSFDWLDLSALDGIEEEVQDIFRDSLFVDEARCHAICQALRGRIERLQEIVHSWHSQSWVDDHSTDVKENIAYSGLQEEEDEWER
>NZ_LN831776.1|WP_020426646.1|6220406_6223106_-|sensor-histidine-kinase-KdpD
MEINQTGDGSILEQLTGMKTGQRRGRLKIFIGYAPGAGKTCAMLKAAHEEQKEGTDVVGGFIETHARPDTLAMLEGLELVPPIKMSYEASVIPEFDLDRALQRSPELILLDDLAHANTAGCRHKKRYQDVEELLRAGIHVYTTINVQQIESLTDIVYSITGMTVQERIPDSVFDSADQVELVDIEPNDLIDRLHKGKIYRDNADEQAMGQLFTKEKLTALREIALRNTASQLNRIAIQISEQAKKNDYDTKDHILVCLSSAASNKKVIRAAARMAEAFHGQFTALFVETPQTQKLTQKNKTELRDNLRLAEQMGANIATVYGEDVPGQIAEYAKTSRVSKIVLGRSPFKKRGYAKSNLVDKLTTLLPNIEIYIIPYTQPSFYKRLPLYARYPKLSLADTNKTIAILVVCTLIGIWFRYLGFLESNIITVYILGVLLSAIVTKGRVYSAVSSVMSVLVFNYFFTEPYYSLNAYEAGYPVTFLVMLAASFITSTLTMRVSEQARQSAQKAYRTEVLLETSRKLQQAKDSPAIIDEMARQMVKLLDRTVIFYSVQEGALSAPLIFPKEGSEVDPHTYTGSNERAVADWVLKNNKRAGATTDTFFGANCLYHAVRGGDTVFAVAAIVMEQEEPLEVFEKGLMIAMLGECALALEKEKLNEKQKEISMQIQQEHLRANLLRSISHDLRTPLTSISGNAGILVGNSGVLSEEQKKGLYTDIYDDSIWLIHLVENLLSISRIENGTLNLNFQAELMEEVISEALLHVNRNSEKHVIHTKLDDELLMARMDSRLIVQVLINIVDNAIKYTQQGSHITVSARQDGHRVIVEISDDGPGISEEAKARLFEMFFTADNIRGDGRRGLGLGLSLCKSIVNAHGGTIGVRDNVPKGTVFYFTLHAEEVNVHE
>NZ_LN831776.1|WP_020426645.1|6219706_6220414_-|response-regulator-transcription-factor
MNKPLILVVEDDKPIRKLITTTLETQGYKYHTAETGEASILEAVSSQPELMILDLGLPDMDGVDIIKKIRTWSNLPIIVVSARSEDRDKIEALDAGADDYLTKPFSVEELLARLRVSLRRIRYDSDKLLKDASSFVNGNLKIDYAAGCVWIGEEEIHLTPSEYKLLCLLAKNVGKVLTHNYILHEIWGSPTVDIPSLRVFMATLRKKIEKTPVQFKYIQTHIGIGYRMLQVGDDS
>NZ_LN831776.1|WP_020426644.1|6219174_6219504_-|hypothetical-protein
MEGLLRNTGLISILLVVLYSIKKLYDVADMRKAGVQGCYENKDIYKAARKFAQGAPEDEVREILSGSYELDGRQIEQTMLLALASRQDRDGGYAAFLKAVNQVLGEDRY
>NZ_LN831776.1|WP_039786108.1|6218963_6219044_-|K(+)-transporting-ATPase-subunit-F
MMWVLGIIVAALFVYLTYALINPEKF
>NZ_LN831776.1|WP_039786114.1|6217263_6218931_-|potassium-transporting-ATPase-subunit-A
MSYIAIAITLLLSLLLARPAGLYMAQVFNYERTGLDRWFGWLEKPVYAIGGIRKENYNWKQYALAAVLSNAMMMLLVYLIFRFQGALPLNPSGIASMEPTLAFNTVISFMANTNLQHYSGESGLSYLSQMLAIVFMMFTSPATGLAVGIAIIRGLTGKPLGNFFVDMVRAITRILLPVCFVLAFVFVALGVPQTLEPTALGHTLEGVTQEIARGPVASFLSIKELGNNGGGFFGVNSAHPFENPDAISNLLQILLMLLLGTGLPFTYGKMVGNKKQGRVLFVSMAMMFIVFLGISLASENAGNPAVNALGIQHQQGSMEGKEARFGVAQSALYSVVTTASETGAVNTMHDTLTPIGGLITIGNMMLNTVFGGVGVGFVNVLMYTMIAVFLSGLMVGRTPEFLGKKIEGKEMKLIAVTLIINPMLILLPTALALLTQSDTLSNPGFHGLTQALYEFTSSAANNGSGFEGLGDATPFWNISTGIVMFLGRYFSIIAMLAVAGSLAAKKTVPETSGTFRTDKALFGAVFLGTVLIVGALTFFPALALGPIAEFLTLKP
>NZ_LN831776.1|WP_020426641.1|6215212_6217240_-|potassium-transporting-ATPase-subunit-KdpB
MSTKKSAINKDIVIQAAKQAFIKLDPRVMLRNPIMFVVEIGFIITLFLVFVPDAFGGDVSTGFNLAVAFILLFTVLFANFAEALAEGRGKAQADSLKKSKKEITANKVSGSSVKEVPSTELRKGDVVIVAQGEMIPGDGEVIEGLASVDESAITGESAPVIKEAGGDFSSVTGGTKVISDRIKVRITSDPGESFLDRMISLVEGAKRQKTPNEIALNTVLVSLTIIFLIVVITLPFFADYLDIRLEVPVLIALLVCLIPTTIGGLLSAIGIAGMDRVTQFNVLAMSGKAVEASGDINTIILDKTGTITYGNRMASEFIPVGKHSRQDVAAWAALSSVRDETPEGRSVLELLKSQNLSFQESVADGAEFVEFKAETRMSGIDLPDGRHIRKGAVDAVKQWVAGQGGIIPDDLQANSNAIASAGGTPLAVAVDQTIYGLIYLKDTVKPGMRERFEQMRKMGIKTIMCTGDNPLTAATIAAEAGVDDFIAESKPEDKIAVIRREQAEGKLVAMTGDGTNDAPALAQADVGIAMNSGTVAAKEAANMVDLDSDPSKIIEVVSIGKQLLMTRGALTTFSIANDIAKYFAIIPAMFMVAIPEMEVLNVMRLHSPLSAILSALIFNAVIIPLLIPLAMKGVAYKPMSSSQLLSRNLIIYGLGGVIVPFAGIKLIDLVVQFWV
>NZ_LN831776.1|WP_020426640.1|6214623_6215196_-|potassium-transporting-ATPase-subunit-KdpC
MKTIAVSIRTTVALMIIILAYQLVVTGIAQAVMPDKADGSLIYNDKHEVIGSKWIGQNFTSPGYFHGRISSIEYNAVSSGTPNYAPSNPDMLERTKASVEAWKSENPGIPVSELPVDLITNSGSGLDPHISVEAAQVQIPRISKSTGISEEQLKELVAKHTQERELGVLGERVVNVLLLNIDVQKTVNGK
>NZ_LN831776.1|WP_020427265.1|6228677_6229277_-|AAA-family-ATPase
MILWINGAFGSGKTQTAFELNRRIPHSFVFDPENAGYYIQKNIPSTLKKNDFQNYSQWREFNYSMLRYIASEFEGIIIVPMTIVEPDYFREIVGRLREDGIKVYHYTLYVSRDRLLARLRSRGEGKHSWAANQIDRCLKGHQHPIFAEQLVTDNMSIEQVAEAIAAKLQISLLPAAPGRMRRFIQRLKVKYQHIRLLDR
>NZ_LN831776.1|WP_020429264.1|6237326_6238208_-|branched-chain-amino-acid-transaminase
MAEQWIYLDGQHVTKENAKVSVFDHGFLYGDGIFEGIRIYNGNIFKCKEHLDRLYDSAKSIMLDIPLTYDEMLEAMAETIRLNDMRNGYIRLIVSRGPGNLGLDPRRCPKASVIIIVEQLAIYPEQAYLNGLRAVSVSQRRNIPDALNPKIKSLNYLNNILVKIQSNLAEADEAIMMNAQGYVTEGSGDNIFIVKRGIVYTPPCYLGALEGITRLAIIELCGKLGLTLKEEPFTMHDVYIADEVFFTGTAAEVIAAREIDGRVIGAGHAGPITLQLLEEFRNVVDKDGYKVWE
>NZ_LN831776.1|WP_020429266.1|6238212_6239100_-|prephenate-dehydratase
MKSIAVLPQGSVSHEALLHLFGDEPVNIEHHKLISNVFLATANGATDYSVIPIENTIEGSVSLHIDWLINEVNLPMQAEWIFPSIQNLISNPQEFVDAEGHKDYSKVVKILSHPVAMAQCLQFIRDHAPWAELESVGSTSEAVEIVSNNPGKGWAAIGTALGAATHGLEVVERQVTDHNNNYTRFVLVGHQKLELPRKSSGDKTSILVTLPEDFPGALHQVLAAFAWRRLNLSRIESRPTKKKLGTYYFYIDVMEPIESVLLPAAIEEINALGCQVRILGSYPTYTYEEEKAEVQ
>NZ_LN831776.1|WP_020429268.1|6239096_6240077_-|homoserine-kinase
MSMYGRSRVKVPASTANLGPGFDTLGMALSLYAWIEMEESAETEFHLYGDEMAGVAKDKSNLLYQVAQMVFSEAGVAVPELSITMYSDIPLTRGLGSSASAIVGGMAAANAMIGSPLSNAKLFDMATALEKHPDNVGASLFGGIITAVWDGEHADYIRIEPPEALEILVVIPDFELSTTKARGVLPSQITVGDAVHNISRTSLLTAALAAGRLDLIGRAMQDRLHQPYRAPLVPGMEKLLAEATGHGALGIALSGAGPTLLCMVDRQESRKPELELFLKQTMEEHGIPARTCWLPPSSSGVAVEQIEPNQMQNRSFLDMIKGEKQL
>NZ_LN831776.1|WP_020429270.1|6240133_6241420_-|homoserine-dehydrogenase
MKPVKVGLLGLGTVGTGVVRIVEGNQEDLSSQVGSPILIERIAVKNTDKPRDIEVDAAAITDDPWDVIRDPEIDVIVEVMGGIAGTKEYILEALERGKHIVTANKDLMALHGSEILAKAQEKQCDVFYEASVAGGIPIIRTLIEGFSSDKIVKIMGIVNGTTNYILSKMSQEGASYHDVLKEAQELGYAESDPTSDVEGLDAARKMAILGTLGFRTNVELSDVSVSGISGVSKEDIAFAKRLGYEMKLLGIAESHEDEFSISVQPTMIRTGHPIASVNGVYNAVYVYGQAVGETMFYGAGAGAMPTATSIVADLVAVIKNLKLGVNGLKQIVPYKQKKLKSDEDIFYKNFLLLHVDDKAGVLAKITQVFAEYDVSLDSVVQQANPSNPDAEIIIVTHNASKASMNKVMRHLEQLKVIHRIKSHYRVEG
>NZ_LN831776.1|WP_020429271.1|6241562_6242000_-|ACT-domain-containing-protein
MKERYYLVREDILPDAVLKTMQVKQLLEAGDAKTVHEGVEQVGLSRSAFYKYKDGIHLIHQLERERIVTISIDLEHESGMLSKVLGSVAVHGANVLTIHQSIPLQGRANVVISVEISHLNEELGDMLDSLKAIPGVKRALIIGQG
>NZ_LN831776.1|WP_020429273.1|6242220_6242970_-|hypothetical-protein
MNMLTGQEGQNTLRLPKYDRPVFDYVIIIIGYLFMPLGLILALVRFAGSHFKNYRKPANISLLYHVFVGGFMQMMVFVIYMVTSAPIDTVTLITMLILFTVLLLLPASGFAASAAKARFKFSQLAQAYVQLINTGGIRYIGNLSEQTGQSESDVRRDLLYLQSHGVLSADLVINEGRTAAAPQELFQEGLSSLPGSSGGQAQPVPQPAAAPAPTQLPKSVRCPGCGAQNTVSPGQSKNCDYCGTTIAYS
>NZ_LN831776.1|WP_020429274.1|6242984_6243731_-|hypothetical-protein
MKRNRKYVSWFTGIYAAVVIFTLGSVVMLGFADSVFRTVVSMIALLIAETAVYAYSLFWLRTAGTAKRTPPVLLSGALIMAVYTAVVFFSTIVLDWMLALQPYWYAGEQLIVLILSAIALGAVGLYGWNAGVQEQRTADASRSLRLHLMEITEIAATARTWSNPGAEELNQLLKDLEEQFKYSDPVSDPAMYETEAVISQQISLLHDHVALLLVLQDPPADWKKETETLTESIASTLQRRNRELAALK
>NZ_LN831776.1|WP_020429276.1|6243743_6244916_-|SPFH-domain-containing-protein
MAIIEVVKYDGPPGVFAWKYPNQELGTWTQLIVNESQEAILFKGGQALDSFTAGRHTLSTANIPLLSNLVNLPFGGKSPFTAEIWYVNKLNSMNVKWGTSAPLQLQDPKYKMMIAVRAFGQFGVRIEEPRKFLLKLVGTLPQFDQSTMLSYFRGLLMSNINELISTYLVHKKISILEINAYVSEISKHIQGRLASTFLESGIELNNFYIDSISIPDDDPATVRLKEALAKKAEMDIIGFTYQQERSFNTMEEAAGNPGSIGAGMVNTGLGLGMGLGFAGPASEMMNRMTRGIMEGGASAAGSTIKTCPSCGAGNSAEARFCSGCGRSLQQPEPEGTPADRTACRNCGEQVVPGAKFCPHCGTSVIIPCAGCGHVLQPGQKFCPECGTRAG
>NZ_LN831776.1|WP_020429278.1|6245105_6246416_-|GTPase-ObgE
MFVDKAKIYVKGGDGGDGLVAFRREKYVPEGGPAGGDGGRGGDVIFRVDEGLRTLMDFRYQRHFKADRGVKGRNKSQHGANAEHMIVRIPPGTVLIDDDTKEVIADMTRHGQQVVVARGGRGGRGNIRFATAANPAPELAENGEEGQERYIVMELKVMADVGLVGFPSVGKSTLLSVVSAAQPKIGAYHFTTITPNLGVVDVGDGRSFVMADLPGLIEGASEGVGLGHEFLRHVERTRIIIHVVDMSGSEGRDPFEDWVKINDELRQYNAGLMDRPQIVAANKMDMPESEANLAAFREQVSELRPDLEIIPISSLTRQGVQELLYRATDLLDSIPVAPVVEEVAETKERKVYKLEAEEDNSFTITRDNDAFVVSSPRIERMLKRMQLSTHDAILKLARTLRHMGVDAELRKRGAVEGTIVRIADFEFEFVENSSYY

Crispr_ID: NZ_LN831776_64

• CRISPR_ID: NZ_LN831776_64
• CRISPR_location: 6490645-6490718
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_64

Consensus_repeat	Method
AAATAGTGATACTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_64

>64.1|6490668|28|NZ_LN831776|CRISPRCasFinder
AGTTTGGGTAACGCAGGGCTATCGAGCA

CRISPR arrays and Neighbor proteins around NZ_LN831776_64

CRISPR arrays

The CRISPR arrays of NZ_LN831776_64

>merge|NZ_LN831776|64|6490645-6490718|CRISPRCasFinder
AAATAGTGATACTTTTTCCACTTAGTTTGGGTAACGCAGGGCTATCGAGCAAATTAGTGATACTTTTTCCACTT

>NZ_LN831776|64|64|6490645-6490718|CRISPRCasFinder
AAATAGTGATACTTTTTCCACTT	AGTTTGGGTAACGCAGGGCTATCGAGCA
AATTAGTGATACTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_039785074.1|6481815_6482892_+|glycosyltransferase	unknown	unknown	gnl|CDD|223515
NZ_LN831776.1|WP_020426401.1|6497164_6498610_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_039785765.1|6501852_6502422_-|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|181835
NZ_LN831776.1|WP_020426398.1|6494556_6495645_-|glycosyltransferase	unknown	unknown	gnl|CDD|226988
NZ_LN831776.1|WP_020425671.1|6484748_6485324_-|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|379312
NZ_LN831776.1|WP_020426405.1|6502675_6504013_-|5'-deoxyadenosine-deaminase	unknown	unknown	gnl|CDD|180895
NZ_LN831776.1|WP_020425672.1|6485358_6486075_-|glycosyltransferase	unknown	unknown	gnl|CDD|133055
NZ_LN831776.1|WP_020425670.1|6483997_6484720_-|glycosyltransferase	unknown	unknown	gnl|CDD|133055
NZ_LN831776.1|WP_020426397.1|6493390_6494524_-|glycosyltransferase	unknown	unknown	gnl|CDD|226988
NZ_LN831776.1|WP_052741527.1|6491531_6493064_-|glycosyltransferase-family-4-protein	unknown	unknown	gnl|CDD|340831
NZ_LN831776.1|WP_046505616.1|6498619_6500518_-|LTA-synthase-family-protein	unknown	unknown	gnl|CDD|293739
NZ_LN831776.1|WP_020426403.1|6500686_6501856_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425674.1|6487069_6487909_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|187564
NZ_LN831776.1|WP_020425675.1|6487905_6488892_-|polysaccharide-biosynthesis-protein	unknown	unknown	gnl|CDD|367154
NZ_LN831776.1|WP_046505611.1|6490136_6490571_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426399.1|6495857_6496631_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|226425
NZ_LN831776.1|WP_020426400.1|6496989_6497175_-|aspartyl-phosphate-phosphatase-Spo0E-family-protein	unknown	unknown	gnl|CDD|378175
NZ_LN831776.1|WP_020425669.1|6482963_6484001_-|glycosyltransferase-family-4-protein	unknown	unknown	gnl|CDD|340831
NZ_LN831776.1|WP_020425673.1|6486071_6487073_-|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|366597
NZ_LN831776.1|WP_020425676.1|6488881_6489976_-|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)	unknown	unknown	gnl|CDD|340819

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_039785074.1|6481815_6482892_+|glycosyltransferase	gnl|CDD|223515	COG0438, RfaG, Glycosyltransferase [Cell envelope biogenesis, outer membrane].	3.819e-27
NZ_LN831776.1|WP_039785765.1|6501852_6502422_-|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|181835	PRK09415, PRK09415, RNA polymerase factor sigma C; Reviewed.	3.08041e-38
NZ_LN831776.1|WP_020426398.1|6494556_6495645_-|glycosyltransferase	gnl|CDD|226988	COG4641, COG4641, Uncharacterized protein conserved in bacteria [Function unknown].	7.99396e-30
NZ_LN831776.1|WP_020425671.1|6484748_6485324_-|class-I-SAM-dependent-methyltransferase	gnl|CDD|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	3.40333e-09
NZ_LN831776.1|WP_020426405.1|6502675_6504013_-|5'-deoxyadenosine-deaminase	gnl|CDD|180895	PRK07228, PRK07228, 5'-deoxyadenosine deaminase.	0
NZ_LN831776.1|WP_020425672.1|6485358_6486075_-|glycosyltransferase	gnl|CDD|133055	cd06433, GT_2_WfgS_like, WfgS and WfeV are involved in O-antigen biosynthesis. Escherichia coli WfgS and Shigella dysenteriae WfeV are glycosyltransferase 2 family enzymes involved in O-antigen biosynthesis. GT-2 enzymes have GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	1.7901e-40
NZ_LN831776.1|WP_020425670.1|6483997_6484720_-|glycosyltransferase	gnl|CDD|133055	cd06433, GT_2_WfgS_like, WfgS and WfeV are involved in O-antigen biosynthesis. Escherichia coli WfgS and Shigella dysenteriae WfeV are glycosyltransferase 2 family enzymes involved in O-antigen biosynthesis. GT-2 enzymes have GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	1.09453e-31
NZ_LN831776.1|WP_020426397.1|6493390_6494524_-|glycosyltransferase	gnl|CDD|226988	COG4641, COG4641, Uncharacterized protein conserved in bacteria [Function unknown].	3.88256e-34
NZ_LN831776.1|WP_052741527.1|6491531_6493064_-|glycosyltransferase-family-4-protein	gnl|CDD|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	2.78681e-31
NZ_LN831776.1|WP_046505616.1|6498619_6500518_-|LTA-synthase-family-protein	gnl|CDD|293739	cd16015, LTA_synthase, Lipoteichoic acid synthase like. Lipoteichoic acid (LTA) is an important cell wall polymer found in Gram-positive bacteria. It may contain long chains of ribitol or glycerol phosphate. LTA synthase catalyzes the reaction to extend the polymer by the repeated addition of glycerolphosphate (GroP) subunits to the end of the growing chain.	5.96902e-90
NZ_LN831776.1|WP_020425674.1|6487069_6487909_-|SDR-family-oxidoreductase	gnl|CDD|187564	cd05254, dTDP_HR_like_SDR_e, dTDP-6-deoxy-L-lyxo-4-hexulose reductase and related proteins, extended (e) SDRs. dTDP-6-deoxy-L-lyxo-4-hexulose reductase, an extended SDR, synthesizes dTDP-L-rhamnose from alpha-D-glucose-1-phosphate, providing the precursor of L-rhamnose, an essential cell wall component of many pathogenic bacteria. This subgroup has the characteristic active site tetrad and NADP-binding motif. This subgroup also contains human MAT2B, the regulatory subunit of methionine adenosyltransferase (MAT); MAT catalyzes S-adenosylmethionine synthesis. The human gene encoding MAT2B encodes two major splicing variants which are induced in human cell liver cancer and regulate HuR, an mRNA-binding protein which stabilizes the mRNA of several cyclins, to affect cell proliferation. Both MAT2B variants include this extended SDR domain. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	6.39617e-67
NZ_LN831776.1|WP_020425675.1|6487905_6488892_-|polysaccharide-biosynthesis-protein	gnl|CDD|367154	pfam02719, Polysacc_synt_2, Polysaccharide biosynthesis protein. This is a family of diverse bacterial polysaccharide biosynthesis proteins including the CapD protein, WalL protein, mannosyl-transferase, and several putative epimerases (e.g. WbiI).	5.97113e-124
NZ_LN831776.1|WP_020426399.1|6495857_6496631_+|AAA-family-ATPase	gnl|CDD|226425	COG3910, COG3910, Predicted ATPase [General function prediction only].	6.79851e-98
NZ_LN831776.1|WP_020426400.1|6496989_6497175_-|aspartyl-phosphate-phosphatase-Spo0E-family-protein	gnl|CDD|378175	pfam09388, SpoOE-like, Spo0E like sporulation regulatory protein. Spore formation is an extreme response to starvation and can also be a component of disease transmission. Sporulation is controlled by an expanded two-component system where starvation signals result in sensor kinase activation and phosphorylation of the master sporulation response regulator Spo0A. Phosphatases such as Spo0E dephosphorylate Spo0A thereby inhibiting sporulation. This is a family of Spo0E-like phosphatases. The structure of a Bacillus anthracis member of this family has revealed an anti-parallel alpha-helical structure.	8.94293e-07
NZ_LN831776.1|WP_020425669.1|6482963_6484001_-|glycosyltransferase-family-4-protein	gnl|CDD|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	2.58049e-22
NZ_LN831776.1|WP_020425673.1|6486071_6487073_-|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|366597	pfam01370, Epimerase, NAD dependent epimerase/dehydratase family. This family of proteins utilize NAD as a cofactor. The proteins in this family use nucleotide-sugar substrates for a variety of chemical reactions.	4.25803e-40
NZ_LN831776.1|WP_020425676.1|6488881_6489976_-|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)	gnl|CDD|340819	cd03786, GTB_UDP-GlcNAc_2-Epimerase, UDP-N-acetylglucosamine 2-epimerase and similar proteins. Bacterial members of the UDP-N-Acetylglucosamine (GlcNAc) 2-Epimerase family (EC 5.1.3.14) are known to catalyze the reversible interconversion of UDP-GlcNAc and UDP-N-acetylmannosamine (UDP-ManNAc). The enzyme serves to produce an activated form of ManNAc residues (UDP-ManNAc) for use in the biosynthesis of a variety of cell surface polysaccharides; The mammalian enzyme is bifunctional, catalyzing both the inversion of stereochemistry at C-2 and the hydrolysis of the UDP-sugar linkage to generate free ManNAc. It also catalyzes the phosphorylation of ManNAc to generate ManNAc 6-phosphate, a precursor to salic acids. In mammals, sialic acids are found at the termini of oligosaccharides in a large variety of cell surface glycoconjugates and are key mediators of cell-cell recognition events. Mutations in human members of this family have been associated with Sialuria, a rare disease caused by the disorders of sialic acid metabolism. This family belongs to the GT-B structural superfamily of glycoslytransferases, which have characteristic N- and C-terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility.	4.73842e-121

Protein sequences

>NZ_LN831776.1|WP_046505611.1|6490136_6490571_+|hypothetical-protein
MADLTAVLPLLSTTGAGATDLTAVLPLLSATGAGAADLTAVLPLLGYDWCGSGGFNSIFAVVGCDWCGSDGFNGSFAVVEYDWCGRGGFNGIFAVVEYDWCGRGGFNGIFAVVGCDWCGRGGFNGIFAVVSDASGKKYSYFSRK
>NZ_LN831776.1|WP_020425676.1|6488881_6489976_-|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)
MKIMTILGTRPEIIRLSVIIPLLDEHAEQHVLVHTGQNFTASLSGIFFAELGLRAPDYVLQDKQAGLGGQLAAMFGSLESILLQEQPDRILLLGDTNSALCAILAERMGIPVVHMEAGNRCYDLKVPEEKNRRVIDAVSTINMPYTQQSKRHLLSEGFPSQRIVLTGNPIHEVIKHYNRQIGASDILDRLNLMAGQYFLVTAHRAENVDDPESLRQIMSGLNLVAEHFGLRLICSIHPRTRSKLAEQFKLEMNPLVEFHEPFGFFDFVHLEQYALCAITDSGTVQEECCLMGVPTVTIRRTTERPETVDCGSNVVSGVEQESILRCTRLMTSLSPEWEAPEGYLTPDVSVKVVKFLLGGNLHVQ
>NZ_LN831776.1|WP_020425675.1|6487905_6488892_-|polysaccharide-biosynthesis-protein
MFNNKRILVTGGTGSWGHELIRQLLPQNPKEIVIFSRSESAQVAMSREYEDSRLSFIIGDIRDKDALVAACRGIDYVFHLAALKHVPVCEDQPYEALKTNVVGTQNVIEAAIACNVEKAIYISTDKAANPSNFYGMTKAIGEKLFVYANLLGSNTRFVTVRGGNVLGTNGSVVHLFMKQIKDKGQVRITDMKMTRFFFTLRDAITLLFKASEVSLGGEIFVMTMPTCRIVDLAEVLIEASGRRDVSIIEAGIRPGEKIHEILMSDFESQTTVVYDEQYLVILPTLDMPELKARYSKYPHVSFNSFSSENNLMDQREIKDILIRGGFLQ
>NZ_LN831776.1|WP_020425674.1|6487069_6487909_-|SDR-family-oxidoreductase
MKLLILGGNGMAGHMLADYFRRQGKHHVFHTTRDKSDLGGLYIDADDIAGVEKLVEIVSPHCIINALGVLNQFAERDRIGAYHVNGFLPHRLRRAADGVHARLIHISTDCVFEGTRGGYTEDDTPDGTSVYAITKSLGEVREPGHLTIRTSIIGPEIRPSGIGLMEWFLAQRGPVSGYRRVMWNGVTTLELAKAIDGLLEPEISGLIHLAHPQPVSKYELLRHMQAAFNKEDVEIIPESAHIQDRTLVSTRADVQVQLPPYPVMLAELAAWMKQPAMSI
>NZ_LN831776.1|WP_020425673.1|6486071_6487073_-|NAD-dependent-epimerase/dehydratase-family-protein
MKTRRILITGASGFTGRHAVAYFHAAGAEVTAVVRSAAAASGIFPAGVKQQVCDLSDRRAVQSMIEEVEPEEVLHLAGKNSVPESWQDPLLYMETNVMSTLYLLEGLRTRPARRILVAGSRLKFKPGLAEGPPHPYSLSKTLEELVSLAWCTLFKQPVLLAEPCNLIGPGPSTGFCSLLAQHIVRSEAAAGTSETLPPFRLSSRFALRDFLDVRDAVRAYDCILRSGEPGKVYRIDSGTLRGLGAVAGQLLAHAAAPVAMDWGPVDTAAEQEAAASAAAVPAALSGALVNQEELSASPEDNAACLGWSPLIELSRSLADIMDYYRASREGGAL
>NZ_LN831776.1|WP_020425672.1|6485358_6486075_-|glycosyltransferase
MRPRVSVVIPFYNCPYIEQALQSALNQSWQPYEIIVVDDGSTMHTDRITPYLPHIHYLGKANGGTASALNHGIRHATGDYVVWLSSDDMFYRDKINNQVLFMDQNRLLITYTNFNYINESTQLTELNAAAVFPSHLDYLRCFLQGNPINGCTVMFKRELFAAIGLFDESLPYTHDYDLWFRAILNGYPPVMLNQSLTAYRRHDGMGTLKHYDAIMAEAAATNARYTPMLRSLIASMGG
>NZ_LN831776.1|WP_020425671.1|6484748_6485324_-|class-I-SAM-dependent-methyltransferase
MYREIKVKDFLPVLLEHLKFAETILDVGSGTGTLLERYEASVVIGLDIHRPYLLHRKYTASHIIPVHADARHIDKLFLPGTFSAVTLIDSLEHFTMSEGKELLRKAEVIAAGRVVVFTPRGFFPQEGTDHYHLQGEYYQKHRSGWEPEDFLGLGYAVTVLKDFHHAENPSFREAFGPNHAPLDALLACKTV
>NZ_LN831776.1|WP_020425670.1|6483997_6484720_-|glycosyltransferase
MNYGTRVSVIIPFYNCSYVHLAIESVLAQSYPDIEIIVVDDGSTLHTEKLLPYSGRIKVLRKANGGTASALNLGITSASGAYFAWLSADDCFHPDKIGRQIAVMLATQTSFNHTAYYYINELGERSSGRISVPFHSKAELIETLMTGCPVNGSTVMVDMNVFKKVGLFNEKLLYTQDYDLWLRILAYYEWSYIEDPLLDYRVHQEMGSIIHSEAQKREIKQVQELHHKSLVRLLRKERRK
>NZ_LN831776.1|WP_020425669.1|6482963_6484001_-|glycosyltransferase-family-4-protein
MRITLPVLTLTRGGAQRMLAELANRLADGGHEVTVLMPSHGIVEYPMRCPVIFAGDTVISEDDFPAGDVIVSNYFTTVPVSQRASEQGKGIHIRLALCYEPTFLPDNNQSFASYHLTPNLLVLSRWQQSIVRINHGIKGRIVPVGLSSDFYNMHIREANKKLIVSAIVRKPEGGFSGHREQEYLLQQLDLIKGQQPEAEICLITPPREYAESSWLQSLFEDGHYRLRTPSSDEELCYHYNESDIFVSSSTYDSGSLPGLEAMRCGAALVTVYSGGNLEYCVHGVNCLMSYRYENRLAEDVVTLIRNMEQRERLSINGAADSLRFTWEKSYNIFQAELYDIVSKRG
>NZ_LN831776.1|WP_039785074.1|6481815_6482892_+|glycosyltransferase
MTLKVLFTFYVPSGGVETLNKLRCESLLRSGIECHVLYLMSGSISQSPASFPVFIAPTDADIKAVLDTHNYDAIIVTSDYLLLERLRRLGYSRILIYESQGLGTRTHAKLLITEAVPFLRSYCNAVLIPPTDHLLELFISICPWLQRYVIPNIVDVQSFRYIPGAAPCDPVIAWVGRLETNKNWSEYLKVAHLIRRSKPDLHLWMFHDPNLATSEQKQLFHEELHALELHDRLNVFTNIPNHVMPVYYSSIAASGGFLLSSSITEGFGYAVAEAVCCTCPVLSTDSDGVRSFIIHNVTGKFYPLGNVEAAVNEGLELMDNLPLRDSIREQGRLHMVSSFGSEKYAQSFREMLNSFAIF
>NZ_LN831776.1|WP_052741527.1|6491531_6493064_-|glycosyltransferase-family-4-protein
MADKATIVLFSHVSNTRSITGAEKLLLFFSRELSPYFNCVLVAPQEGKLTRQARNNGLNVQLLTIPLVYGMYTPYAGLEPDIRKFQEKLEYCELVEWLAALRPAFIISSTCVHALPAMAAKSLGIPVVWKISETITDNDFTSISTELIHKNSDEILAISHTAASCFPEDIRAEKVTLLPPSWNDSEMMFEAWSKLRSERRRDLRVAPKEPLIGYISSFINKEKGLEHFVKMAVLVSKEHPEAKFMVVGTPGDKSYYDRCVRKVKLEGLTSHFKFVGYEESLPEVYCAMDMLVVPSLIREGFGMTALEGLAFGKPVVAYASGGLYEILHAAGCGELLAPVGDIDQLAQRVNGLLAEPGLAAVVGSQARERVDAVYGPAAYRARLLGLAEKWHLRYCPALPEPVSAPEPPAAAEASDSSEPAPPLQLEPQPEAVPPPEPEPQRRKHASRAARLRRGKLRRGKLRRAASRARSRPRPGRKRRAAGSARRRSSGGKHRRAGHARRKAKRRRKAA
>NZ_LN831776.1|WP_020426397.1|6493390_6494524_-|glycosyltransferase
MNNNFVIPAPPLPRTPAEEEKLRGRLSGFKVGYDEGYLRGRLAILDGRPEEPLPVRNIHVMYVASGKGYPYSPLDDAVLYALQKLTTQVTITDVRQNLVELVGAQRPDLVLVLDGMDLPLDQVAVLRSKGIKTAIWLTDDPYYTDFTVKIVAHYDYVFTLEQNCVEFYRGLGCPEVHYLPFAAHREHYRPTTGRSPVSRDISFIGSAYWNRVHFFREIMPELMSYNTIINGIWWDRLPEAPLYGERIEIGKWMTPQETAVTYSGSKIVINLHRSHIDEAANNNTLLIPAVSPNPRTFEIAASGTLQLCDARDDMGTFYTVGEEIDTFTTPREMMDKIRYYLTHEEERRAMALRAFERTLKDHTYTRRLHKLLTIIYG
>NZ_LN831776.1|WP_020426398.1|6494556_6495645_-|glycosyltransferase
MKSKKRKVHPPDYRDGYQEGYRLGLCEAVRRLNSPEVGACRPLKLMYVPQGFQAIDAGVTEALGQLVSELVISSPETMLETAARESPGAVLVMNGLHVFPDNHLEQITEIRKLGIPTAIWFVDDPYFTEDTSVICKHYDHVFTHELGCVEFYHDLGVNSVHYLPLCVNPQMFYPRRTGPQYQFDVVFIGNAFRNRTELFDGLAPFLQGKKVLIAGGFWERLSTYEELSPFIKDGFIPPEETANYYSGAKLVINIHRPWEGGQDNRNSFQLPSRSINPRTYEISACGTMQLTDVREDLGNYYRPGKDLDTFENSDELKFKIDYYLNHEKDRRQIALQGLRTTLRHHTFISRLPHLLNVLTAQV
>NZ_LN831776.1|WP_020426399.1|6495857_6496631_+|AAA-family-ATPase
MYAMDNAMLYIRNAELLRERVPSFQAYPFDLPVIRSFNRLDFQNRVTFLVGENGTGKSTLLEGIAAAWGFNPEGGTLNFSFNTRSSHSSLHEYLRLTKGVRRPKDGFFLRAESYYNVASYIDQLDEEPGEQFQIPMIKDSYGGKSLHEQSHGESFFAAFVHRFGGQGLYILDEPEAALSPLRQMSLLVRMHELAEQHSQFIIATHSPILMSYPGADIYLLEGEGIRPVPLEETEHYTVTKAFMNDRAGMLRELLGDG
>NZ_LN831776.1|WP_020426400.1|6496989_6497175_-|aspartyl-phosphate-phosphatase-Spo0E-family-protein
MGDKQHQARIEQARKELHSLALELGISHPKVLSQSVKLDMLINEYIECQTDEPGDITRRDH
>NZ_LN831776.1|WP_020426401.1|6497164_6498610_-|hypothetical-protein
MKRWFKAENLIALAGCGLIIYLLFVQPFVGVADNGDFKRMMNTVGLDYYNAAESYADRFFSFSHSRFAYGDLFLGFYPSSQILLVLVPRLLAGLVHGSYFDIRLLAAVYALLLLAATWMIVKLGGSRSYITGLLLGAGMLIVFYDIGYLAYFNSLFGEPVSMVSMLLTFALGLRLAGQERPTTKGLTLFFIAVLFLVCSKIQNAPVGLAFSLIFLRLMTLNGTGNWRKLAMRFAVAVCLVSVIMYVAAPKELKHINLYQTVFFGILNESPDVRGDLRELGLPEKLEVLAGTNYFQSGTAIKQDDPSLQADFYDRVSHKDVLFYYIKHPSRLVDGMKFAARNSMDLRPYYLGNYEKSEGKPEKALSYAYSTWSQFKREVLPHSLGFLAIFYLLYYAGVLFEYFRSRDLRGRIAGELLMLLGLIGLFSFLVPIMGDGRADIGKHLFLFNVSFDMMAVVMFGWAVHKLVRLVQSVAGKSGQYGR
>NZ_LN831776.1|WP_046505616.1|6498619_6500518_-|LTA-synthase-family-protein
MNENKPVRVGGPFYIVAGLVWLKLLLLRGLFFDRIAWEWIAADLAPVLLLMGILALVIPARIRTGVYWTFNGLLSLLLFAASVYFNHFGSVPTYLAFYELNQVFQVKESVESTIQSIDYLFFADLVIAGVYRLFRRWKRGVSHPLRRYVSPGARRVQWIVILVSIIGGGALSAYSVHAARGVTNELVQAESAGFLNYEVFAAMKSQEDNGLIGTGDIRETIAKIDALEATYPYSGKPAGTMPDYFGSQQGKNVIVIQMEAFQNFPLHQSLDGQELTPVLNSLAGEGFYFPHVYQQIGAGNTSDAEFMSNTSIYPIATLAMSTGFGDRVLPSLPRLLRDKGYEAYTFHVNKVGFWNRNELYPALGFNGYYEKGDFKNDHFNAFGASDEQLYITAVEKLAALQSKGTPFYAQLVTASSHHPFKIPDAFKRITLPDSLQNTMLGDYLTAINYTDYAIGTLIDGLKQNGLWDNTVLVLYGDHFGLQPKDVPPEQVEEALGIPYDSRISRFNIPLIMHVPGMAQGKVVKQTGGQLDILPTLANLLGVSLKQEGFTAFGHDLLNIDRNVVGMRYYSPTGSFFNNEIMFVPGKGFADGEAVSLDTLQPVADIDKYQSDYEYILKLMGLSDEYVKLLPQR
>NZ_LN831776.1|WP_020426403.1|6500686_6501856_-|hypothetical-protein
MKEREPKWYEEARNGPFRESRFTEAAADKVIMQVRSGAPGLERTGNKLRLSFIVAAIILLLAGTGALLQQKGLLGEGRQAGMFYHEVKTPDLTDAGLRKTAERIMQEQLGKKLPVVSLERMERINEVRIVFEDGEYTSTLRINTEIGQVTEWNMNVFYPLKEIDPQLINEAVVNLRDNGYEGNFTVTGLERSSQYSLVSNREVRTHDVLLGKEGRIDYENGIYAGATINLNRNEVSEEVIQKSDRALKLLRGEREDHLYQITRGLAAKWDVIILKYGEDENGPSTVIMDYATHEILHVQDNSLHIEESYDSKIHGEQDTKILTMDNAKLQSSAAVIADELFGIRLEDYTVVNKMIGNILFESPSGDSRIYAAYNDEGVFYAMVRQITTP
>NZ_LN831776.1|WP_039785765.1|6501852_6502422_-|sigma-70-family-RNA-polymerase-sigma-factor
MQDLAHAAAMSEEQLRQIMGFYGNDVWHYIYYLTKSADIADDLAQEVFIKCFYRIGTYRGSSSFKAWLFTIARNTVFSYRKSRFFRSGFWGGVQAIRNNEPVRNSWPDELPGTARSAEMEYLGNCRTDEIWSIILQLPDKFREVLVLDLKAELSIQEIAGLTGLSPGTVKSRLHRARHKVQEKLRGMES
>NZ_LN831776.1|WP_020426405.1|6502675_6504013_-|5'-deoxyadenosine-deaminase
MENILIRNAEIITMNKQEEIIYGDIRIRDNLIAEIGSGLVAQGDERVIDARNRTVIPGFVQTHIHLCQTLFRGKGDDLELMDWLRKRIWPLEAAHDEESLYYSAMLGIGELISSGTTTIVDMETVHHTDFAFQALAKSGIRALSGKVMMDQKNADAPAALQEETAASLQESVDLLEKWNGYGNGRIQYAFSPRFVISCTEPLLREVRDLSERYGVRVHTHASENLGEIEIVQAMTGMRNIVYLDHLGLANERLILAHCVWLDDEERRILRDRGVHVSHCPGSNLKLASGIANTPGMLHDHIHLSLGADGAPCNNNLDMFNEMRLAAMIQKPQHGPTTMDARSVFRMATIGGAKAVGMEDQIGSIEVGKKADLAILNLYNFHTFPSFDVDPISRIVYSATRADVETTIADGEILMDKGLLKTVDKDTVLHEANRSIKRLLAQTPLA

Crispr_ID: NZ_LN831776_65

• CRISPR_ID: NZ_LN831776_65
• CRISPR_location: 6640937-6641022
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_65

Consensus_repeat	Method
GGCTTGGCCCTGAATGCCGGGCTGCGTCC	CRISPRCasFinder

spacers of NZ_LN831776_65

>65.1|6640966|28|NZ_LN831776|CRISPRCasFinder
AGTAAGTACCGGGATTCCTTCCTTAGAT

CRISPR arrays and Neighbor proteins around NZ_LN831776_65

CRISPR arrays

The CRISPR arrays of NZ_LN831776_65

>merge|NZ_LN831776|65|6640937-6641022|CRISPRCasFinder
GGCTTGGCCCTGAATGCCGGGCTGCGTCCAGTAAGTACCGGGATTCCTTCCTTAGATGGCTTAGCCCTGAATGCCGGGCTGCGTCC

>NZ_LN831776|65|65|6640937-6641022|CRISPRCasFinder
GGCTTGGCCCTGAATGCCGGGCTGCGTCC	AGTAAGTACCGGGATTCCTTCCTTAGAT
GGCTTAGCCCTGAATGCCGGGCTGCGTCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020425791.1|6629075_6631259_+|glycosyltransferase	unknown	unknown	gnl|CDD|133005
NZ_LN831776.1|WP_020425786.1|6637558_6639055_-|hypothetical-protein	unknown	unknown	gnl|CDD|133029
NZ_LN831776.1|WP_020425787.1|6636245_6637562_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425778.1|6646023_6651066_-|family-16-glycosylhydrolase	unknown	unknown	gnl|CDD|185693
NZ_LN831776.1|WP_020425789.1|6633074_6635120_+|glycosyltransferase	unknown	unknown	gnl|CDD|133005
NZ_LN831776.1|WP_020430209.1|6625211_6626231_+|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_LN831776.1|WP_020425779.1|6645366_6645924_+|hypothetical-protein	unknown	unknown	gnl|CDD|224427
NZ_LN831776.1|WP_020425773.1|6655958_6656927_+|iron-hydroxamate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|238558
NZ_LN831776.1|WP_020425790.1|6631255_6633055_+|glycosyltransferase	unknown	unknown	gnl|CDD|133005
NZ_LN831776.1|WP_020430210.1|6626373_6627051_-|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|224561
NZ_LN831776.1|WP_039785171.1|6651304_6652321_+|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_LN831776.1|WP_020425788.1|6635493_6636249_-|glycosyltransferase	unknown	unknown	gnl|CDD|133005
NZ_LN831776.1|WP_020425783.1|6641309_6641921_-|VTT-domain-containing-protein	unknown	unknown	gnl|CDD|378149
NZ_LN831776.1|WP_020425774.1|6654142_6655795_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_020425780.1|6643908_6645108_-|glycine-betaine/L-proline-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|226643
NZ_LN831776.1|WP_144412158.1|6628125_6628935_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425781.1|6643078_6643912_-|proline/glycine-betaine-ABC-transporter-permease	unknown	unknown	gnl|CDD|226644
NZ_LN831776.1|WP_020425782.1|6642195_6643065_-|glycine-betaine-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270357
NZ_LN831776.1|WP_167345704.1|6652880_6653897_-|beta-ketoacyl-ACP-synthase-3	unknown	unknown	gnl|CDD|237245
NZ_LN831776.1|WP_141639034.1|6639263_6639962_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020425791.1|6629075_6631259_+|glycosyltransferase	gnl|CDD|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	1.01669e-45
NZ_LN831776.1|WP_020425786.1|6637558_6639055_-|hypothetical-protein	gnl|CDD|133029	cd04186, GT_2_like_c, Subfamily of Glycosyltransferase Family GT2 of unknown function. GT-2 includes diverse families of glycosyltransferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	9.0668e-10
NZ_LN831776.1|WP_020425779.1|6645366_6645924_+|hypothetical-protein	gnl|CDD|224427	COG1510, COG1510, Predicted transcriptional regulators [Transcription].	1.08417e-40
NZ_LN831776.1|WP_020425789.1|6633074_6635120_+|glycosyltransferase	gnl|CDD|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	5.86549e-45
NZ_LN831776.1|WP_020430209.1|6625211_6626231_+|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	2.66411e-100
NZ_LN831776.1|WP_039785171.1|6651304_6652321_+|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	1.11925e-100
NZ_LN831776.1|WP_020425773.1|6655958_6656927_+|iron-hydroxamate-ABC-transporter-substrate-binding-protein	gnl|CDD|238558	cd01138, FeuA, Periplasmic binding protein FeuA. These proteins have predicted to function as initial receptors in ABC transport of metal ions in some eubacterial species. They belong to the TroA superfamily of periplasmic metal binding proteins that share a distinct fold and ligand binding mechanism. A typical TroA protein is comprised of two globular subdomains connected by a single helix and can bind their ligands in the cleft between these domains.	2.25575e-74
NZ_LN831776.1|WP_020425790.1|6631255_6633055_+|glycosyltransferase	gnl|CDD|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	1.00161e-53
NZ_LN831776.1|WP_020425788.1|6635493_6636249_-|glycosyltransferase	gnl|CDD|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	1.30684e-16
NZ_LN831776.1|WP_020425783.1|6641309_6641921_-|VTT-domain-containing-protein	gnl|CDD|378149	pfam09335, VTT, VMP1, TMEM41, and TVP38 (VTT) domain. The VTT domain was previously called the SNARE-associated domain, but was renamed as there seems to be no evidence for association with SNARE proteins.	2.21993e-18
NZ_LN831776.1|WP_020425774.1|6654142_6655795_+|helix-turn-helix-domain-containing-protein	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	8.78353e-26
NZ_LN831776.1|WP_020425780.1|6643908_6645108_-|glycine-betaine/L-proline-ABC-transporter-ATP-binding-protein	gnl|CDD|226643	COG4175, ProV, ABC-type proline/glycine betaine transport system, ATPase component [Amino acid transport and metabolism].	0
NZ_LN831776.1|WP_020425778.1|6646023_6651066_-|family-16-glycosylhydrolase	gnl|CDD|185693	cd08023, GH16_laminarinase_like, Laminarinase, member of the glycosyl hydrolase family 16. Laminarinase, also known as glucan endo-1,3-beta-D-glucosidase, is a glycosyl hydrolase family 16 member that hydrolyzes 1,3-beta-D-glucosidic linkages in 1,3-beta-D-glucans such as laminarins, curdlans, paramylons, and pachymans, with very limited action on mixed-link (1,3-1,4-)-beta-D-glucans.	1.09559e-101
NZ_LN831776.1|WP_020425781.1|6643078_6643912_-|proline/glycine-betaine-ABC-transporter-permease	gnl|CDD|226644	COG4176, ProW, ABC-type proline/glycine betaine transport system, permease component [Amino acid transport and metabolism].	1.67496e-124
NZ_LN831776.1|WP_020425782.1|6642195_6643065_-|glycine-betaine-ABC-transporter-substrate-binding-protein	gnl|CDD|270357	cd13639, PBP2_OpuAC_like, Substrate binding domain of Lactococcus lactis ABC-type transporter OpuA and related proteins; the type 2 periplasmic binding protein fold. This subfamily is part of a high affinity multicomponent binding-protein-dependent transport system specific to betaine compounds for osmoregulation. The periplasmic substrate-binding domain, which is often fused to the permease component of the ATP-binding cassette transporter complex, is involved in uptake of osmoprotectants (also termed compatible solutes) such as glycine betaine and proline betaine. Many microorganisms accumulate these compatible solutes in response to high osmolarity to offset the loss of cell water. This domain belongs to the type 2 periplasmic binding fold protein superfamily (PBP2). The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.07856e-135
NZ_LN831776.1|WP_167345704.1|6652880_6653897_-|beta-ketoacyl-ACP-synthase-3	gnl|CDD|237245	PRK12879, PRK12879, 3-oxoacyl-(acyl carrier protein) synthase III; Reviewed.	0
NZ_LN831776.1|WP_020430210.1|6626373_6627051_-|alpha/beta-fold-hydrolase	gnl|CDD|224561	COG1647, COG1647, Esterase/lipase [General function prediction only].	2.02486e-39

Protein sequences

>NZ_LN831776.1|WP_141639034.1|6639263_6639962_+|hypothetical-protein
MNISSSAIHSGALVNSTAQNNRITSTSSGSANFNLMLSKAATADTAALIAQQYGLSVGVESIPKNEQEIVSRGSRGNLQDVVIAPDIVEQMKTDSKLAEKIKGYIDHYANVDLPAFAQMDAMYGVTNVGSSLIIHEDGTKTVWSASVTSPEEVEKGRKIEAEKQKEKAEERERLEALHVPNQTMTAALGNLPYSKHTPPGNTGDLALYQGISSQEWLHQRSLFISKKRNELV
>NZ_LN831776.1|WP_020425786.1|6637558_6639055_-|hypothetical-protein
MSDSNHSVRNERLAGRYSYLEREGLLPLPVQDGITVVVELRYAAWAWECLNLLQQHSGASISLIGVAMDTDFPLQPLTEAFPGAAFIPYEPGKYGVNEALAYAGTSFVALLEDRVMVTPGWVGNLLWPFIDDPSVQVAAPRSSTEQGEARERLHFGTEQELSAYVTHSLERRQGEWHEAPVLCGSCLVFTRELLQRIGGFDSTLVKRQLMVADWCLRARQRGGRLVLSDALYVHSLQPLLEARAKAEHEGMQDGVQAYLAKWGLDHSAVNVEEGILPVPPDVSALPPRPGIMLEKSTAAPVPLVTAVVYSERPLMLTPEEFCESQKRLQGQQSYGNIRWVWIRDSRRDALPEYPVREQDAVIAVQGEDSWLHALENVAALYDSEIVVYLSASADYDSHYVKRIAEAVLHGSADLVVSRADSAIEEPASVQSLPLLIPVKLPLERIAHRSGSVPGRITRQKVSGHGLQLEPQPSLAIGYIGGPPEANILTRCSGGEVRL
>NZ_LN831776.1|WP_020425787.1|6636245_6637562_-|hypothetical-protein
MNYLILSHVPWEDYPYKRLLDLLPERAEVCFAGAMTSDQQADSGIRPVSLAELKTLDGKRYTILVSSPYWLQDVLALKPRYIVALLEPCPEGEDNTMWNKYSALLAARADLVGTASERLYLEQNLYRPKVVYLGGDHPLSCGLMRRGDQLFFLTDYEAIWIQALTELWQPASPGAGGWLFIQHRLRADFYVSMCGKMPVQPTVHYLAATYLYLLGDEAAGRYLARSFELMLLHDYTDCLHSHYRFFSAIEAKKSNLELAVAQYEITAFTEEERKTAMQMRQWLDNGQSELLQAEIYRVNEDIAEAVRILENLSCPEAQPLLLQNYITSFQWDKALQLQRESGLSGSDAGNIPLPDGAVLPISATHPASAVLLAGTEIPVYGGIQLPVIEGTLHLLHGRRHAAIRSFLRVAGAGGEARTLFAEMADLEEAVGRLKGEDR
>NZ_LN831776.1|WP_020425788.1|6635493_6636249_-|glycosyltransferase
MINKGRPLRKTSGNRLTAMMQVRNESGRYLEQVLEELSGFVDDIVIVDDASTDGTVRLCESFAKVTKLVTLEGSRFNREWELRRILWELAVSTDPDWLLSVDADEFYEEEAKREMRRLIDQDVYDWVAFRLYDFWGGTTHYREDEHWNIHTKHTRTLVRYLPQFYYFTPQMDHHVPRLPLSYAVLPGFLTELRVKHYGWALPPEALREKYDRYMELDPEGKWGSLEQYASILDENPRLVEWQERRRLGRPE
>NZ_LN831776.1|WP_020425789.1|6633074_6635120_+|glycosyltransferase
MSIPDLSLCMIVKNEAQHLERCLSSVAGLVSEIIIADTGSTDNSVEIALSFGARVLEISWEGDFALARNLTLRQATCSWILVLDADEAVSGWPADALNVLLGAEHVHGYFLPFIHYVGDAANGEYVTDNVCRLFRNDERIKFRGTIHEEAASSIWALAGGKIAYAALPVRHYGYLEDELRRKDKSARNLKLIHEALRHDPASLPLQYALGTEYYQLGEYGTAADVLLPLLKSAPADPGYFADIYLKTAYALQSSGRPEEAKAVYKEGLRLFPDFTDLLESCAALLLEEGQLLEPYHLLQKALESGDTSQHYPSSSGSGTSRTSLLMGQVCERLLRYEEAADYWEQAIGFDPSCAAAWAELVPLCLLAGGEHRLTALTRRILQALPPDLLGRCVPAALNAHAWAWLQVLSTAPQLPASVQSVLRVLPELSRQHPQALDAAAALPELLREGPEQPSIHGYLWAWSCRTGDAAAAGQWLASLAASRPGLAAVHHRIWEESGGGRAAAQQRHPPGGPAAMPPCYADHPGSPAAVPLAFPDLSYAAQLLLQTGAWSSLLRLYRNTSPAVFQWCRLPQPLLRGLIQAPVPFREQWCSIYSSHAQQSGGAAGSPAEWLLYAAIAASCGRVPQLNPAAENALRQSGSAAAAGGLSYHKLLLAAEAFPDSGLQGRIPWLLLVRTALRDGL
>NZ_LN831776.1|WP_020425790.1|6631255_6633055_+|glycosyltransferase
MKPRNRISLCMIVKNEADNLPQCLKSVRGVADEIVVVDTGSTDSSVQIARSYGARIVNFPWSGDFAAARNAGLKAARGQWILVLDADEELDQGSAGELLLCAEHMEYEAFFLRIHNHRGTSRSSETITVNPILRMFRNRPAYRFSGIIHEQIASVIVREKPAAAMHLSTVVIHHYGYADGVVAKKDKIRRNVDLLKEQLKRSPGDAFHHFNMAVEYMRLGEYDHALEHIHVSLEHVEPDTSYVHLLHKYEIRCLAVKGDVQGALAACERGITLFPDYPDLHHIKGVLLLQTAAWKEAKEALRQALDIGVSPPGYHTEAGCGTYATLSLLGQLCQETGEDYEAAAFYTKAARLHPEPWPLIARLVRTMKCSGRESELNGWLELHLPPAAAEHRKLAVLLLNEGCYGAAAELLEKSGFNDALGPMGQRGASAAETGSVGAEQCKLPSVGCGESLVQQGAGRMADSEGAGNCDGAETRDGADSSDSAGKGEPVTGSDAPAAQGSAGSPGTVIEDSGSFVMALQKTAAAPAASLRQEDIAVLLEHSCSIPGQGTGLISTPAYQHSRSWMLLADFVLASLPASAASSPAAGKARQLLPLPRMTD
>NZ_LN831776.1|WP_020425791.1|6629075_6631259_+|glycosyltransferase
MKKPTLGVHLIIRNEAALLPQCLDSLHGAADEIVIVDTGSTDNSAAIAASYGAKVYHMNWNNDFSAARNTGLSHAETDWILVLDADEILKTPVGAITEMLRNTEAMAFTVNIENWIGSLPEDRLTHNAIRLFRNGAGYSFQGIIHEGLDASVIGKHGASVIRSSGIEIIHLGYLPGIMAQKDKISRNEQLLRRALAKDPGNDFYSYNLAVTCCQNGQLEEAAELLTRTISRAPLQASYRPSMIRDLAKIQLSLNHTQAVNALLARELPRYSDYPDLHFIQGQSWESQGLTERAFQSYQRAAAGSEEPAAPVDASSTGATEEADTAVSAGAALNAGAVVNAEATLYAGAALSGKYVSEKGMNSFRPLARMGEISLQLGHCEEAARWFHRALQHHVLYAPALQGIASAFQRLDVPDQDIATLLIQLVGTGEAAGRSAVIHALDAVCAYEAIAGLPQTDFPLEQETLPARASAWIITGRLAEAGTALREALSPLRDTATMDGDMDTIHRLWMIAAICRWQDNSPQAEPLEFADAPEPLRSALLLVDEQLTQHNTALALPGEAGNLPQVIAELIRQAVKLRCCGLAAELAGLFPEHRADWAEALYESGQLKEAGELLIALAADQQVRGKVSFYLAELLFDKGHYREAAEWFQLMLDGTPGHEPSRIGLALSYLHLARLELEGAAAGFPEIYTNGPLQEDMKAAEQAIAVLNRTAWHTQCNPHRTLQKGATP
>NZ_LN831776.1|WP_144412158.1|6628125_6628935_+|hypothetical-protein
MLDGTITSVLGATITAGTLSSAGTVTNLLDGTITSVLGATITAGTLSSAGTVTNLLDGTITSVLGATITAGTLSSAGTVTNLLDGTITSVLGATITAGTLSSAGTVTNLLDGTITSVLGATITAGTLSSAGTVTNLLDGTITSVLGATITAGTLSSVTSISQRSFIELATTGITTADAFTPLPANTTSVLGTYSYFIVNTGANPVNTQVEISADGTNYFVDTTGDNPLPAGSVDVIVPSRFLKYTRLAYQSATPGAASTLNVIFDAQGT
>NZ_LN831776.1|WP_020430210.1|6626373_6627051_-|alpha/beta-fold-hydrolase
MESCLFIHGFTGGEYEISPLAQFLERHDYHARTFTLKGHGGSRNDLLQSDRHDWRQSAEDQLQDLLLGGEGVHLIGFSTGALIASYLSVQYQDCIKSLTLLSTPVFPLNLLEIARTLGSPVMVRNYLSKFGTTPAKATREFLRLVRESFNIYPQIKIPTLIVQGRRDHLVRAKSAAYLQRTIPSGSKRVLMVERSGHMLCHGEHSGQMMNEVLQFMRTSGRTGLN
>NZ_LN831776.1|WP_020430209.1|6625211_6626231_+|LacI-family-DNA-binding-transcriptional-regulator
MKVTITDIAIAAGVAKSTVSKVLNDSPKISQETKQKVREIMKQMNYTPSSIATGLARQSSSNIGLLIDMSKSSEFLNQFFYNIIGGIESVIGSLKYELTIANVEHNHPDGHFLHRLVRSKRVDGLIANTSVLTEELCTRLNHLEFPYVSLGEVAASGCWVDFDNEAGGRMLTRHLLEEGYSAVAFIGGYEGDPLFIRRLEGCRQVLGQAGKPLRKEWIINGEAEEAFGYQAAKQLLLSETPPDSVICMSNFAAYGVLLAARELGVKVPTQLGIATFDDYPLSRYTSPPLTSLNLDTFHLGVSAGKLLMERIGGKNEALQKLLLAPELLPRESSCRHTRT
>NZ_LN831776.1|WP_020425783.1|6641309_6641921_-|VTT-domain-containing-protein
MTETINAWIDWLLQSLGLSGPYILLVTIPLTVLQSLFGFFPLAVLIVLHVSVFNVIGGMLVSWLACNVGAMLSYFLFRRFLFDWFDRKWRSKLKRYDKWQRYLDRYGVWTLVLLRTVPIMPSNVINFMSAVSPMKVPAFIWGTVLGNLSYIWLFGTLGSTLIVSREEWNGFLLWYGVFVVILIGIFIRRHWGHLQEDKRRRME
>NZ_LN831776.1|WP_020425782.1|6642195_6643065_-|glycine-betaine-ABC-transporter-substrate-binding-protein
MKKKTWGILMLILLVAVAAGCSSSSSKAKTVKLAYVAWDSEIASTNVVKEVLESKLGASVEMLQVDAGPMWAGIADGSADAMVAAWLPSTHASYLEKYGQDMEDLGANLEGTKTGLAVPAYMDIKSIEDLKNAGVAKSLNNQIIGIEPGAGIMTASQKAIDAYGLSDYTLLESSSAAMAQELQKAYTDNKPIVVTGWTPHWMFANMDLKYLDDPKGVYGGAEQIHTMVRKGLKEDMPDVYRFLDQFQWTPEDMAQVMGEIQGGKSPEDAAKAWVSEHEDQVNTWIAGIE
>NZ_LN831776.1|WP_020425781.1|6643078_6643912_-|proline/glycine-betaine-ABC-transporter-permease
MNIPKLPLGKAVEWLENWLTTYLGPFFDFIHAVIGGMVNGIETALTVLPALVLILIITALAYWIGKWRMALFALAGLLLIDNLGLWGPSMQSLALVLTASVLAVLIGVPLGVLCAQSNGVQNTVTPVLDFMQTMPAFVYLLPAVSFFSLGVVPGVIASIIFAIPPTIRLTNLGIRQVSPELVEAADAFGSTSGQKLFKLQLPIALPTIMAGINQTIMLSLSMVVISSMIGAQGVGAYVYRAVSQAKTGAGFEAGIAIVIIAILLDRLTQKLVKPKKG
>NZ_LN831776.1|WP_020425780.1|6643908_6645108_-|glycine-betaine/L-proline-ABC-transporter-ATP-binding-protein
MAIIEVKQLTKVFGHDAVRALPLLAQGWSKEKIAREAKLTVGVNRADFRIEEGEIFVIMGLSGSGKSTLVRLLNRLIEPTGGQVLFRDKDVVKMNPEQLRQFRRKNIGMVFQKFALFPHRTVLANAEYGLEVQGVEKKERTRLAMQALELVGLKGWEHHHPDQLSGGMQQRVGLARGLANDPDILLMDEAFSALDPLIRKDMQQELLELQSKMKKTIVFITHDLDEALRIGDRIALMKDGVIVQIGTPEEILIQPANKYVERFVEDVDLSKVLTAAHVMRQPEMIRPERGPRVALQLMRDSGVSSLYVADKEMKLQGVVTAEDAAQALKENRPILEVMRREIPRVSPDTLLNDLFELMSETHLPVAVVDEADKLKGIVIKGAVLSALAGNAVPEGEGMR
>NZ_LN831776.1|WP_020425779.1|6645366_6645924_+|hypothetical-protein
MNDLVGLAPEQVERISKARERVIDSIGKNMDLYGITLSIGHLYGYMYFNQGPVTLDELSRTMGMSKTSMSTGVRTLLDLKMIDKVWGKGTRKDLFEVVPDWHQNFSDYFSIKWRKAVEGNMSALSKSLNEIRQMKSDYADEPGVEQLLNTDEVKIEEAIKYYRWLLKLIEALETGKIFELIPKES
>NZ_LN831776.1|WP_020425778.1|6646023_6651066_-|family-16-glycosylhydrolase
MKKKASALLTVMALLSGLLSPLGGGHIAGAASGQSVKAADSAVQTGSVTAAEGKSSGYNGLKAFTDVPADSWAARAVQRWIENGIVAGYGDGSFRPDAPVSKAEFAVIINRIFNYSAKSATLPDDVPAAAWFSSEIAKGIAAGYLIASKDGRIEASAPLTRAETAVALQKIFRLDTGGQAAYSDLAGTDHEVRDAAAALSGAGYVKGYPDGSFKPQGRITRAELAQTLDRMVPGLVRSAGEVTLGKVQGNVVLNHAGITLKDTVVEGNLYLSEGIGEGKIILEGVKVTGTTFILGGGEQGVGLQNSVIGRVQAGKPDGDIRMYASGTTSVGTVLLNSGATLEETGLTGTGFTDVEISAAVKAAVLKGSFAAVSTASSATGSVKLTLSGKVGKLTLGSPGQVVLADHAQVAELLLTAAAKGTALQGSGSFGAVVNNAEGVTVSGVPLKPGSSGPVAVPPAATQAPAGGSGTSPTATPTATATVTPTASATPRATATPTATATPTATATPTSPADPWTLVWNDEFNDGTIDPAKWTYDLGDGTAVGNPGWGNNELEWYTNEEKNVKEADGKLIITARKEAQGGKEYTSSRIKTKDLFSKKYGKFEIRAKAPAGKGYWPAIWMLPEDYVYGSWAASGEIDIMEGWGSRPGTVAGTIHYGSQWPDNVYSGKEYVLPGNSTIEQFHTYSLEWEPGELRWYVDGVLYSTKNDWYSLSNGQPANNAYPAPFNQEFHLLMNLAVGGNFDGNPTAETVFPQSMEIDYVRVYELTGRPYRQPVPVTLTKEPYLEGSLPPLADGNLIYNNGFTEHKEGDTGMGIPNTAHWVLYKESGADAAVSLEPISGRNYLKVNISSPGGNSYSIQPQAIVSLAKGRFYKLSFDAKTDHSRNIGVRLTGGESRGYQAYSPTLKAELTSTLKHYETMFQMKENPDIAARVEFNLGTNASPVWLGNARLEEIDSIPFDHDSAKTPLGSGNHLYNGTFDLGEPDRLSYWHAEATGGAAVSPSVDAAGRLNLQISGTGGDGADVRLLQNGIFLVQGQDYKLAFDVEVPSPRTAIIELQGRDGTVYASETVLLKAGAQKVEAVFPDLAGASDTLGRFVLHLGNAAGIVQLDNFLLLRTSFYYDPSLVYYPLVNGDFSFGFNSWERLLTEQGGAATAAVTEGAATFNIANTGNQPYSVMLFQNGLKVAGGTDYVIEFDASSSVARRISVNAENASYQPSFTQIIKITPETNHYRFEFRQGVNDTLALKFLLGKVDGVSIPQAHELVIDNVRFEIKNAPAKPQELLGDSTNNRVSQPVELTFTENAAWRSSITAVKVNGTALAEGQYTVQAGKITIEPAAFPAEGSYMITVEAEGYVSATVTQTILANDNNLVVNGSFVSGTTGWSTWSGEGGVSSFNVNEGVAEIRIDVAGTAAWHTQFYQEGIPLEAGKTYELSFKAKSTVPRQIIVEYSGTSAAAAQAKFEVTATWATYSARFTVDNSNPLKLNYLIGAAMGEDKTANGIPHTLSFDDIRVTEVEGGGGTPVEPASGKLDNGTFDPAKGLTGWTQYFDGTGSAAAQDGELAVALTGTGTANYSAQVDYANLKLVQGKTYTLAFAARSDVDRLIEVAVEHKGGDYTKYLPAKAVALTGSMNTYSYTFTMDSGTDAGAHLVFLLGLVAGNSEGTNSAIQAGNHIYIDNVSLTEAP
>NZ_LN831776.1|WP_039785171.1|6651304_6652321_+|LacI-family-DNA-binding-transcriptional-regulator
MNIKKIAEMAGVSVSTVSKIINNYSDVSEKTKKRVMEIIEQTGYSPSNSAKTLATKKSSLIGVIFAGELNVEFTHPFFVEVLNAFKKQMGVLGYDLIFFSNEKFISSGDYYSRCLHFNVDGCVIISGQKMEPAIRDLDMSSIPCIGVDLELRGKKSGYVMSDNVQIASKVVEHFYLLGHRELGFIGSTADSDISNQREAGFVKAVESFGLTLNRNWFVHGDDFFESSGYTAMRRLLESGSMPQAVFAASDLLALGAIRALKEQGLRIPEDVAIIGCDDIEACKYTSPTLTTIRQNKERLGVLAAHMLYDLINNQSDGGSFVVEPALIVRESCGSKLTG
>NZ_LN831776.1|WP_167345704.1|6652880_6653897_-|beta-ketoacyl-ACP-synthase-3
MLLKGAKITAIGAYVPARRLTNSDLEQMVDTNDEWIVQRTGIRERRISREDEYTSDLCAAAVLDLMKRYGKSMHDVDMILVATSTPDFPFPSVASILQNRLGIPATAGAIDMSAACAGFVYALHTAHAYVASGLHRKVLVLGADALSKITDYTDRSTCILFGDGAGAVLVESGEQLDGFAGFHLGSDGSGAHHVYRTGLSHRVNEVELSDTGKLVQNGREVFRWAVRTVPQGVQQVLNNAGIGLDQVDWFIPHSANLRMIEPICERLNYPFEQALYSLEYFGNTSAASIPLALDLGVREGKVVNGQQILLYGFGAGLTQAGQLVKLELAPEVSPPTPL
>NZ_LN831776.1|WP_020425774.1|6654142_6655795_+|helix-turn-helix-domain-containing-protein
MNTLVPEWAESHFPLYTFDGIQSMYGTSNLPSVQIHENQTVLIAIAAGKGSLEVNNQHYELMEGGIVLLPANTYATLTTNPRQPLHAYKLSIRFLEQTRVMPAGTMMQKSGIASDSKLLLFPYEPAIVSDVKELYLHRLPDRETRHVQNQLLFHQILLQLLEQQEARYIASGQPSMERSITYLENHFSEKITREHLAAIAGVSRSHYSTLFKQLTGFTLNEYLSRLRVHRAKELLLNSSGTLREIALKVGYKDEFYLSRRFKQETGTSPSGYNRKPIRHVAVLLTPYASHLLLLGLEPAVTISESSEYLNLSGQEPPKPMKFINTNSSAAQMRSALLEANIELIIAARQHLDQLRLSPGELRAVAPIVEIPWMEMGWKDHLRLIGQAIQRSERAEQWLADFEKEEAEARAIVQQSTGGKEIITILVIKPDGLLVYGSRNVGCVIYQSLGLRAPALIEAEMKKLGDQFHSFPIDISELAEYAGDRLLVVVFPDAKGSTAHTEAVFRSPHWKRLPAVQRKNVHWLERDEWVPYNPVSIRLQLGRAVALFDSK
>NZ_LN831776.1|WP_020425773.1|6655958_6656927_+|iron-hydroxamate-ABC-transporter-substrate-binding-protein
MKKIFIPFVLILGIVLSACGGNQAKVPGPSSSPAGNSANNSSTASSSEPEGSTFTYESENGPVEVPKNPQRVVVLTRFLTGNVMALGVPVVGVDEMSKTNPRFEEKLKDVEAVSDESLEKIIELQPDLIIGLSDIKNIDKFKQIAPTVTYTYNKVDYLTLQLQVGKLLNKEKEAQAWVDDFKARTEKAGEEIRAKIGKEATVSVIETFNKQLYVYGYNFGRGTELLYGAFKLGMPEKVKEGTKTDGYLAVSTEVLKDYLGDYVIFSKNAEEDNSFQNTDIYKSIPAVQNNHVFEADAKAFYFNDPLSLEYQLEFFEHSFLGK

Crispr_ID: NZ_LN831776_66

• CRISPR_ID: NZ_LN831776_66
• CRISPR_location: 6889473-6889577
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_66

Consensus_repeat	Method
CCCCGCTCTCTCTGCATGTTTCTC	CRISPRCasFinder

spacers of NZ_LN831776_66

>66.1|6889497|57|NZ_LN831776|CRISPRCasFinder
GACCCGCTTATCCCCTTCTCGCCGCTCCACTCCCACTCAATAATCCTGTGCGCATTC

CRISPR arrays and Neighbor proteins around NZ_LN831776_66

CRISPR arrays

The CRISPR arrays of NZ_LN831776_66

>merge|NZ_LN831776|66|6889473-6889577|CRISPRCasFinder
CCCCGCTCTCTCTGCATGTTTCTCGACCCGCTTATCCCCTTCTCGCCGCTCCACTCCCACTCAATAATCCTGTGCGCATTCCCCCGCTCTCTCCGCATGTTTCTC

>NZ_LN831776|66|66|6889473-6889577|CRISPRCasFinder
CCCCGCTCTCTCTGCATGTTTCTC	GACCCGCTTATCCCCTTCTCGCCGCTCCACTCCCACTCAATAATCCTGTGCGCATTC
CCCCGCTCTCTCCGCATGTTTCTC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020426270.1|6881631_6882543_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224054
NZ_LN831776.1|WP_020426274.1|6883317_6883851_-|RNA-polymerase-sigma-factor-SigY	unknown	unknown	gnl|CDD|182010
NZ_LN831776.1|WP_020426840.1|6895435_6896221_-|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|131480
NZ_LN831776.1|WP_020426278.1|6885473_6886088_-|DedA-family-protein	unknown	unknown	gnl|CDD|223659
NZ_LN831776.1|WP_020426271.1|6882542_6882734_-|hypothetical-protein	unknown	unknown	gnl|CDD|379161
NZ_LN831776.1|WP_020426276.1|6884274_6884904_-|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|293792
NZ_LN831776.1|WP_020426845.1|6899135_6900443_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_039786342.1|6897335_6898055_-|pirin-family-protein	unknown	unknown	gnl|CDD|380375
NZ_LN831776.1|WP_020426272.1|6882783_6883005_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_141639044.1|6883001_6883331_-|DUF5345-family-protein	unknown	unknown	gnl|CDD|375100
NZ_LN831776.1|WP_020426842.1|6897017_6897242_+|DUF1128-domain-containing-protein	unknown	unknown	gnl|CDD|377674
NZ_LN831776.1|WP_020426030.1|6890521_6891715_-|SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|379330
NZ_LN831776.1|WP_020426280.1|6886751_6887405_+|SdpI-family-protein	unknown	unknown	gnl|CDD|379303
NZ_LN831776.1|WP_167345705.1|6893503_6894796_+|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_LN831776.1|WP_020426029.1|6892068_6892731_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426275.1|6883909_6884086_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046505765.1|6884910_6885477_-|thioredoxin-family-protein	unknown	unknown	gnl|CDD|379658
NZ_LN831776.1|WP_020426028.1|6892994_6893498_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|378968
NZ_LN831776.1|WP_020426844.1|6898302_6899139_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226354
NZ_LN831776.1|WP_081487115.1|6896326_6896905_-|spore-protease-YyaC	unknown	unknown	gnl|CDD|131888

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020426270.1|6881631_6882543_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	1.27287e-97
NZ_LN831776.1|WP_020426274.1|6883317_6883851_-|RNA-polymerase-sigma-factor-SigY	gnl|CDD|182010	PRK09638, PRK09638, RNA polymerase sigma factor SigY; Reviewed.	7.17388e-71
NZ_LN831776.1|WP_020426278.1|6885473_6886088_-|DedA-family-protein	gnl|CDD|223659	COG0586, DedA, Uncharacterized membrane-associated protein [Function unknown].	6.9676e-47
NZ_LN831776.1|WP_020426271.1|6882542_6882734_-|hypothetical-protein	gnl|CDD|379161	pfam13396, PLDc_N, Phospholipase_D-nuclease N-terminal. This family is often found at the very N-terminus of proteins from the phospholipase_D-nuclease family, PLDc, pfam00614. However, a large number of members are full-length within this family.	0.000628983
NZ_LN831776.1|WP_020426030.1|6890521_6891715_-|SAM-dependent-methyltransferase	gnl|CDD|379330	pfam13679, Methyltransf_32, Methyltransferase domain. This family appears to be a methyltransferase domain.	1.57051e-50
NZ_LN831776.1|WP_020426845.1|6899135_6900443_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	8.88202e-67
NZ_LN831776.1|WP_039786342.1|6897335_6898055_-|pirin-family-protein	gnl|CDD|380375	cd02910, cupin_Yhhw_N, Escherichia coli YhhW and YhaK and related proteins, pirin-like bicupin, N-terminal cupin domain. This family includes the N-terminal cupin domains of YhhW and YhaK, Escherichia coli pirin-like proteins with unknown function. YhhW is structurally similar not only to human pirin but also to quercitin 2,3-dioxygenase (quercitinase). Although the function of YhhW is not completely understood, YhhW and its human ortholog have quercitinase activity and are likely to play an important role in transcription and apoptosis. This N-terminal cupin domain of YhhW has a metal coordination site and is thought to have catalytic activity while the C-terminal cupin-like domain has diverged considerably and has closer alignment with C-terminal pirin. YhaK is found in low abundance in the cytosol of E. coli and is strongly up-regulated by nitroso-glutathione (GSNO). There are major structural differences at the N-terminus of YhaK compared with YhhW; YhaK lacks the canonical cupin metal-binding residues of pirins and may be involved in chloride binding and/or sensing of oxidative stress in enterobacteria. YhaK showed no quercetinase and peroxidase activity; however, reduced YhaK was very sensitive to reactive oxygen species (ROS). Proteins in this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold.	9.02959e-57
NZ_LN831776.1|WP_020426840.1|6895435_6896221_-|alpha/beta-fold-hydrolase	gnl|CDD|131480	TIGR02427, b-ketoadipate_enol-lactone_hydrolase, 3-oxoadipate enol-lactonase. Members of this family are 3-oxoadipate enol-lactonase. Note that the substrate is known as 3-oxoadipate enol-lactone, 2-oxo-2,3-dihydrofuran-5-acetate, 4,5-Dihydro-5-oxofuran-2-acetate, and 5-oxo-4,5-dihydrofuran-2-acetate. The enzyme the catalyzes the fourth step in the protocatechuate degradation to beta-ketoadipate and then to succinyl-CoA and acetyl-CoA. 4-hydroxybenzoate, 3-hydroxybenzoate, and vanillate all can be converted in one step to protocatechuate. This enzyme also acts in catechol degradation. In genomes that catabolize both catechol and protocatechuate, two forms of this enzyme may be found. All members of the seed alignment for this model were chosen from within protocatechuate degradation operons of at least three genes of the pathway, from genomes with the complete pathway through beta-ketoadipate. [Energy metabolism, Other].	1.89006e-37
NZ_LN831776.1|WP_141639044.1|6883001_6883331_-|DUF5345-family-protein	gnl|CDD|375100	pfam17280, DUF5345, Family of unknown function (DUF5345). This is a family of unknown function. It is found mostly in Bacteria. Members of this family are predicted to contain 2 trans-membrane regions.	4.61263e-20
NZ_LN831776.1|WP_020426276.1|6884274_6884904_-|MBL-fold-metallo-hydrolase	gnl|CDD|293792	cd06262, metallo-hydrolase-like_MBL-fold, mainly hydrolytic enzymes and related proteins which carry out various biological functions; MBL-fold metallohydrolase domain. Members of the MBL-fold metallohydrolase superfamily are mainly hydrolytic enzymes which carry out a variety of biological functions. The class B metal beta-lactamases (MBLs) for which this fold was named perform only a small fraction of the activities included in this superfamily. Activities carried out by superfamily members include class B beta-lactamases which can catalyze the hydrolysis of a wide range of beta-lactam antibiotics, hydroxyacylglutathione hydrolases (also called glyoxalase II) which hydrolyze S-d-lactoylglutathione to d-lactate in the second step of the glycoxlase system, AHL lactonases which catalyze the hydrolysis and opening of the homoserine lactone rings of acyl homoserine lactones (AHLs), persulfide dioxygenase which catalyze the oxidation of glutathione persulfide to glutathione and persulfite in the mitochondria, flavodiiron proteins which catalyze the reduction of oxygen and/or nitric oxide to water or nitrous oxide respectively, cleavage and polyadenylation specificity factors such as the Int9 and Int11 subunits of Integrator, Sdsa1-like and AtsA-like arylsulfatases, 5'-exonucleases human SNM1A and yeast Pso2p, ribonuclease J which has both 5'-3' exoribonucleolytic and endonucleolytic activity and ribonuclease Z which catalyzes the endonucleolytic removal of the 3' extension of the majority of tRNA precursors, cyclic nucleotide phosphodiesterases which decompose cyclic adenosine and guanosine 3', 5'-monophosphate (cAMP and cGMP) respectively, insecticide hydrolases, and proteins required for natural transformation competence. The diversity of biological roles is reflected in variations in the active site metallo-chemistry, for example classical members of the superfamily are di-, or less commonly mono-, zinc-ion-dependent hydrolases, human persulfide dioxygenase ETHE1 is a mono-iron binding member of the superfamily; Arabidopsis thaliana hydroxyacylglutathione hydrolases incorporates iron, manganese, and zinc in its dinuclear metal binding site, and flavodiiron proteins contains a diiron site.	2.40718e-70
NZ_LN831776.1|WP_020426280.1|6886751_6887405_+|SdpI-family-protein	gnl|CDD|379303	pfam13630, SdpI, SdpI/YfhL protein family. This family of proteins includes the SdpI and YfhL proteins from B. subtilis. The SdpI protein is a multipass integral membrane protein that protects toxin-producing cells from being killed. Killing is mediated by the exported toxic protein SdpC an extracellular protein that induces the synthesis of an immunity protein.	2.41847e-16
NZ_LN831776.1|WP_167345705.1|6893503_6894796_+|MFS-transporter	gnl|CDD|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.43743e-56
NZ_LN831776.1|WP_020426842.1|6897017_6897242_+|DUF1128-domain-containing-protein	gnl|CDD|377674	pfam06569, DUF1128, Protein of unknown function (DUF1128). This family consists of several short, hypothetical bacterial proteins of unknown function.	3.46916e-27
NZ_LN831776.1|WP_046505765.1|6884910_6885477_-|thioredoxin-family-protein	gnl|CDD|379658	pfam14595, Thioredoxin_9, Thioredoxin.	1.51426e-49
NZ_LN831776.1|WP_020426028.1|6892994_6893498_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|378968	pfam12840, HTH_20, Helix-turn-helix domain. This domain represents a DNA-binding Helix-turn-helix domain found in transcriptional regulatory proteins.	4.08265e-09
NZ_LN831776.1|WP_020426844.1|6898302_6899139_-|sugar-ABC-transporter-permease	gnl|CDD|226354	COG3833, MalG, ABC-type maltose transport systems, permease component [Carbohydrate transport and metabolism].	3.94983e-104
NZ_LN831776.1|WP_081487115.1|6896326_6896905_-|spore-protease-YyaC	gnl|CDD|131888	TIGR02841, Uncharacterized_protein_YyaC, putative sporulation protein YyaC. A comparative genome analysis of all sequenced genomes of shows a number of proteins conserved strictly among the endospore-forming subset of the Firmicutes. This protein, also called YyaC, is a member of that panel and is otherwise uncharacterized. The second round of PSI-BLAST shows many similarities to the germination protease GPR, which is found in exactly the same set of organisms and has a known role in the sporulation/germination process. [Cellular processes, Sporulation and germination].	1.82293e-42

Protein sequences

>NZ_LN831776.1|WP_020426280.1|6886751_6887405_+|SdpI-family-protein
MKDFKWKWQDTVIVILGVLSLGYALANYGKLPDQLPAHFDIRGEADRYWSKGSVIAFTGFLGLIFPLAMQFIKSVDPKKENYSKFQNAYKMIRLAIAALFDAMLVLTVSYGLNQNIPAGKIAMVAIGLLFIVVGNFMPQIRDNYFTGIRTAWTLASPEVWRKTHRFSGVMWMIGGLLIALGAFLPQSLSISMIIAALVIAIILPFAYSWLISSRTKA
>NZ_LN831776.1|WP_020426278.1|6885473_6886088_-|DedA-family-protein
MHVISDLISHLFEWIQSLGYFGIMIGLMIEVIPSEIVLAFGGYLVSQGEINYFGAVLFGTVGGVIAQIFVYWIGRYGGRPVLEKYGKYIFIKKKHIDHSEEWFNKYGTGVIFTARFIPVVRHAISVPAGISRMPLGKFTLLTTLAVIPWSALFVYLGYTLGDKWETIDEVAAKYTHELILAAIAIIVIYFLFKWYKSKKKGSAV
>NZ_LN831776.1|WP_046505765.1|6884910_6885477_-|thioredoxin-family-protein
MKQNVAHKFGQGLTPRQFVEGMTKNQQAFESWYEKFAWEDQDDRAYFESLNHRDDLRVLILAADWCGDVVRNVPVVFRILETAGIKTEVLILEENQDVMDDFLTMGGRSVPIVIFADTGGYVLGHWGPRPEHVQSLMREFKRENPDREAPDYESKIAEVRKAMGQAYGEGTESHAVIAKELRSLISGF
>NZ_LN831776.1|WP_020426276.1|6884274_6884904_-|MBL-fold-metallo-hydrolase
MLNIRSYNLGPLQTNAYLLTGADPGRGVIIDPGANPAALLRAAQEMEIEAVLLTHAHFDHIAGLDEIRRAKKCPVYLHTLESEWLGSPKLNGSLMWPDVTPPISTEPAEYDLADGQVLNLLGLTFRVMHTPGHSPGSVSFLCGSDLFSGDVLFKLGVGRTDLTGGRERDLIDSIRNKLYRLDEEVRVFPGHGPRTTIGFERQCNPYVPM
>NZ_LN831776.1|WP_020426275.1|6883909_6884086_-|hypothetical-protein
MKDTEEEVHEEEAHKAPISTTGGQDKKECLFWSFPHGKGAIQPWRRRLWELQNNSDRE
>NZ_LN831776.1|WP_020426274.1|6883317_6883851_-|RNA-polymerase-sigma-factor-SigY
MSDGTHERIIRAQHGDASALAVLLQEHYAFLYKYLVKATMNPLLAEELAQDTMVRCMEKIGTYNGASSFSSWLITIATRLYIDRKRRWKLEMKWKRQEEGVRSIRWRFESRNLEWSEVLDALSRLSSVQRMAVLLKHYYGYGYEEIADILQIPSGTAKSRVAAGLNQLRKELSDDEH
>NZ_LN831776.1|WP_141639044.1|6883001_6883331_-|DUF5345-family-protein
MMNTEKDDELLQMLSGDLERLDAQYDDISPPSLPGLKRLIAEEALRRQHQRRRELQMFLLVALFMVSIVMVSLGLAPVIYWILQAAVPIAGLGCLAVVRLRLRREDAEE
>NZ_LN831776.1|WP_020426272.1|6882783_6883005_-|hypothetical-protein
MKELQDVPYWLWGCLAAALLLQGTLIFRNAQKRGRGRVAWFWGIWGLTGIPTPLICYLLFVVLPDRKRANRKL
>NZ_LN831776.1|WP_020426271.1|6882542_6882734_-|hypothetical-protein
MEEIKWGLIWPLLALQVLLAVIGLVSLGKAEQTRGPKWLWVIILIFGNLLGSVAYFTVGRKDN
>NZ_LN831776.1|WP_020426270.1|6881631_6882543_-|ABC-transporter-ATP-binding-protein
MPLLTVANLRKVYGGHTPVDGISFDIEAGKCVALLGPNGAGKTTTLRMLAGLLKPTSGQISFEGGPVGDYRKRIGYLPQSPAFYNWMSGQEYVVFAAKLYGVSSKEAAGLAADVLEHVGLRDAARRKIGGYSGGMKQRLGLAQALIHRPRLLLLDEPVSALDPIGRREVMELLRGIREDTTVIFSTHVLHDAEEICDDIILMNHGLIAEHGALSRLRSQYSIPVIRLTTEREEKAQRWLEDLAHRSFVEQSAVSSGSATLNVKNVELARQIILQEAGNLDIPLLQFEAGSSTLEDLFMKVVGA
>NZ_LN831776.1|WP_020426030.1|6890521_6891715_-|SAM-dependent-methyltransferase
MYPVESLNALIEQVMSGRTLITATLSQLRSKGETTYTKVQVKPVELKGKLHYQFAYYTGPKVEHRNIPAESAAAELMSLFREKFRQGLLCTVEADYQVLISKKYKVSILTKSPSKQEAPNLDHNRRKRYVLDEGEPVPFLVELGIMNSEGKVLAKKYDKFRQINRFLEMVEDVLADLPTGRPLTIVDFGCGKSYLTFALYHYLAIREQRELNIVGLDLKADVIEHCSALAAKLGYGKLRFLVGDIADYNELEQVDMVVTLHACDTATDAALEKAVRWGASVILSVPCCQHELFAQIESGVLNPLLSHGILKERFSALATDAIRAKLLDLMGYRTQLLEFIDMEHTPKNILIRAVKGASGDNAAKWREYSAFRDFLGAKPYLERVCTDLLPGESTVQG
>NZ_LN831776.1|WP_020426029.1|6892068_6892731_-|hypothetical-protein
MFRRDYIVRMIEDMTAMVAKVMTLKQEKKTTEALWEVDELLIRHFRLNSRLLNSLSVEDIIDMYLLGGVVESDKLQGVARLLKEEGAIYTAAGDKDAGLFRAMRSLHLFLYADLHGADRTLLQMPADIDELLRETQAYSLPAKTERLLLSYMESLGRYAKAEDSLYRLWEQGEDVVQEGKELYSRLLLKSPEELELGGLPEQEVRDGLKEWERRTAAVRQ
>NZ_LN831776.1|WP_020426028.1|6892994_6893498_+|helix-turn-helix-transcriptional-regulator
MNEDKEYQASIQRQPLKVSPEQEKLLESALRIKIMHLLAAEPLTSKQVAEKLEKTPGNVHYHISKLFEGGLLELVRTEAAGGIIQKFYRSKATWFRAENFSGFQFRAEDQVDHFTTRLTLSPEELESFRREMMDFISSWESRVTLGTEYGVDIVIGHLRTPEPEVNP
>NZ_LN831776.1|WP_167345705.1|6893503_6894796_+|MFS-transporter
MPASTSESGKTNPFRGFAAPFAKSRAFPFLWLGHLISFLGSSVTMVILPVLVYSLTGSTTTMGVVMAVYMLPNILMLPVSGHIVDRYDRVGIMMLADIFRALIMLATAVLALTGLLSIPLLLILIGCYGLLDGLFQPAYAAVRATVFTPDIRVTANSVTQITTQTVRLIGPALGGLLITHLSAGIGFGLDAFTYVFSFICLIYLRRALIARVRTDASGTAGSMAAPSPSADWKQDFMEGLAVLRSHPWLWITILAFSFINICYGGITSILVPWLFKVQHGWDPYLYGLAVTCSGAGAILAGLIFGTRQRWSRRGLMAYGGAFISGVSLLLLPFVPSAAGAVILFSLEGFGLMVFMLIWEISMQELVPQEAFGRVASLDLLGSFALLPVGYILVGWLADLIGGVATIAIFSGLGMACIALVLSIPAIRNFQ
>NZ_LN831776.1|WP_020426840.1|6895435_6896221_-|alpha/beta-fold-hydrolase
MEIVRCEGSNICYSDQGTGDVIVLLHGFCGSSSYWEQVIPLLSGNYRVIAPDLRGHGVSDAPLGAYSIDQMADDVLSLLDALEIPECYLLGHSLGGYITLSFAQRHASRLKGFGLIHSTGYPDSGEARENRLKSVSMIQNEGIFAFVDGLVPGLFAPGAAPQLLERTKEIGYRTPPQGAVGAAMAMRERPDRRDVISATALPVLLVAGAEDSKVTPEQTFTSNKPNVTQATISGVGHMSMYEAPERLAEIIKDYVHAAVRK
>NZ_LN831776.1|WP_081487115.1|6896326_6896905_-|spore-protease-YyaC
MCHKKQKEARTLAIREQESRKRKKRDASGLIFFFREIASQHPPEQITFLCIGTDRSTGDALGPLTGSQLLEQGFPHVSGTMPSPCDADNLEARIAEIPAGQIVIAVDACLGPPASLGYFLTADEPLRPAQSVGLNLPAVGHYSLAAIVDVYGPRPYRTLQSTPLHRVMVMAKQIALAAAAGFGMETGKAFQD
>NZ_LN831776.1|WP_020426842.1|6897017_6897242_+|DUF1128-domain-containing-protein
MDLSQPTQENVEYMIEGIKSKLKMASAAAMQASAFSVKNYEDILDIYEVAMGSDRLSISQVEALVSELGRLRDK
>NZ_LN831776.1|WP_039786342.1|6897335_6898055_-|pirin-family-protein
MIKVITSAERHTSNREWIHSEFSFSFADYDDPSNAHFGALLAHNDNELSPGQGMHEHPHHDLEIITYVVSGVLKHQDDLGNHAELQGGSVQVMSAGTGINHSETNPSDSEHVRFLQIWLLPDQPGRQPKWDAKFYPAEHKTNTLLPVASGKGEEGALEIHENVTVYLSSLERSRELKYQQREDRRTHIYLISGHLEIACSDGVFQLEPGDAARIRKSCDLHLKGTGSDSNAEFILIDLP
>NZ_LN831776.1|WP_020426844.1|6898302_6899139_-|sugar-ABC-transporter-permease
MNRKPEEAAKTIGSYALLILLSFISLFPAFWIVMSSFKTGNSLFSDTLIPRRMTLVHYQELFEQTKYLQWFLNTLKVAALSTLIGTSLLLLASYAISRYRFAGRKSMLTAFLVLQMFPGFMAMIAIYVLLNTLGLLNSHWALVLVYSSGSIITNVFVAKGFFDTIPKSLEDAARIDGASHMKVFLSIMMPLSKPMLTYASLMIFNGCFVDFIFADLILRTEEKRTLAVGLFRMVNQSNSTEFTLFAAGAVLVALPVTLLFIFLQRFLIDGLTAGAMKG
>NZ_LN831776.1|WP_020426845.1|6899135_6900443_-|sugar-ABC-transporter-permease
MPKKTGAAVLSAVIPGLGQMYNRQWLKGLAFLLTGMAWFYFMTHGLTGHLRGLITLGELPSRMVKVGKMTRMVEGDHSIFMMINGLMALLALLLYCGFYLLNIRDAFMVGAARARQEQIRSFGQSLKYMGRRHFAYLVLAIPLTAIVFLTILPLVFSVLLAFTNYADPILPPANLVDWVGFGNFKKMLSLDVWSTTFGGILTWTLCWAVIATVTTYIGGVLVAVLIHQPRVRFKKLWRTLLIVPFAIPNMISLLVMRNMFNNQFGPVNKYLGMIGLNGLPWLTDPFWAKVTVILANMWIGIPVTMILAFGVLTTIPRDLYEAAEVDGAGSAHKFRMITLPMVLFATAPILIMQFAGNINSFNVIYLMTNGEPVNPHYQYAGDTDLLVTWLYKLALNQSQYSFASVIGIIIFLLVATFSIWSYRRTRSYKEEDMIT

Crispr_ID: NZ_LN831776_67

• CRISPR_ID: NZ_LN831776_67
• CRISPR_location: 6894872-6894945
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_67

Consensus_repeat	Method
AAGTGGAAAAAGGATAACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_67

>67.1|6894895|28|NZ_LN831776|CRISPRCasFinder
CGCCCGGGTACCCTGTTCTCCGCAGCTG

CRISPR arrays and Neighbor proteins around NZ_LN831776_67

CRISPR arrays

The CRISPR arrays of NZ_LN831776_67

>merge|NZ_LN831776|67|6894872-6894945|CRISPRCasFinder
AAGTGGAAAAAGGATAACTAATTCGCCCGGGTACCCTGTTCTCCGCAGCTGAAGTGGAAAAAGGTTAACTAATT

>NZ_LN831776|67|67|6894872-6894945|CRISPRCasFinder
AAGTGGAAAAAGGATAACTAATT	CGCCCGGGTACCCTGTTCTCCGCAGCTG
AAGTGGAAAAAGGTTAACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020426849.1|6904174_6904678_+|YtxH-domain-containing-protein	unknown	unknown	gnl|CDD|378938
NZ_LN831776.1|WP_020426848.1|6902237_6903989_+|alpha-glycosidase	unknown	unknown	gnl|CDD|200477
NZ_LN831776.1|WP_039786345.1|6900462_6901761_-|maltose-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270304
NZ_LN831776.1|WP_020426278.1|6885473_6886088_-|DedA-family-protein	unknown	unknown	gnl|CDD|223659
NZ_LN831776.1|WP_020426029.1|6892068_6892731_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426276.1|6884274_6884904_-|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|293792
NZ_LN831776.1|WP_020426850.1|6904831_6905164_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426845.1|6899135_6900443_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_039786342.1|6897335_6898055_-|pirin-family-protein	unknown	unknown	gnl|CDD|380375
NZ_LN831776.1|WP_020426840.1|6895435_6896221_-|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|131480
NZ_LN831776.1|WP_020426842.1|6897017_6897242_+|DUF1128-domain-containing-protein	unknown	unknown	gnl|CDD|377674
NZ_LN831776.1|WP_020426844.1|6898302_6899139_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226354
NZ_LN831776.1|WP_020426030.1|6890521_6891715_-|SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|379330
NZ_LN831776.1|WP_020426280.1|6886751_6887405_+|SdpI-family-protein	unknown	unknown	gnl|CDD|379303
NZ_LN831776.1|WP_167345705.1|6893503_6894796_+|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_LN831776.1|WP_020426275.1|6883909_6884086_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_052741532.1|6887707_6890377_-|hypothetical-protein	unknown	unknown	gnl|CDD|225844
NZ_LN831776.1|WP_020426028.1|6892994_6893498_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|378968
NZ_LN831776.1|WP_081487115.1|6896326_6896905_-|spore-protease-YyaC	unknown	unknown	gnl|CDD|131888
NZ_LN831776.1|WP_046505765.1|6884910_6885477_-|thioredoxin-family-protein	unknown	unknown	gnl|CDD|379658

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020426848.1|6902237_6903989_+|alpha-glycosidase	gnl|CDD|200477	cd11338, AmyAc_CMD, Alpha amylase catalytic domain found in cyclomaltodextrinases and related proteins. Cyclomaltodextrinase (CDase; EC3.2.1.54), neopullulanase (NPase; EC 3.2.1.135), and maltogenic amylase (MA; EC 3.2.1.133) catalyze the hydrolysis of alpha-(1,4) glycosidic linkages on a number of substrates including cyclomaltodextrins (CDs), pullulan, and starch. These enzymes hydrolyze CDs and starch to maltose and pullulan to panose by cleavage of alpha-1,4 glycosidic bonds whereas alpha-amylases essentially lack activity on CDs and pullulan. They also catalyze transglycosylation of oligosaccharides to the C3-, C4- or C6-hydroxyl groups of various acceptor sugar molecules. Since these proteins are nearly indistinguishable from each other, they are referred to as cyclomaltodextrinases (CMDs). The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues (Asp, Glu and Asp) performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase.	0
NZ_LN831776.1|WP_039786345.1|6900462_6901761_-|maltose-ABC-transporter-substrate-binding-protein	gnl|CDD|270304	cd13586, PBP2_Maltose_binding_like, The periplasmic-binding component of ABC transport systems specific for maltose and related polysaccharides; possess type 2 periplasmic binding fold. This subfamily represents the periplasmic binding component of ABC transport systems involved in uptake of polysaccharides including maltose, maltodextrin, and cyclodextrin. Members of this family belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	7.22673e-127
NZ_LN831776.1|WP_020426278.1|6885473_6886088_-|DedA-family-protein	gnl|CDD|223659	COG0586, DedA, Uncharacterized membrane-associated protein [Function unknown].	6.9676e-47
NZ_LN831776.1|WP_167345705.1|6893503_6894796_+|MFS-transporter	gnl|CDD|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.43743e-56
NZ_LN831776.1|WP_020426276.1|6884274_6884904_-|MBL-fold-metallo-hydrolase	gnl|CDD|293792	cd06262, metallo-hydrolase-like_MBL-fold, mainly hydrolytic enzymes and related proteins which carry out various biological functions; MBL-fold metallohydrolase domain. Members of the MBL-fold metallohydrolase superfamily are mainly hydrolytic enzymes which carry out a variety of biological functions. The class B metal beta-lactamases (MBLs) for which this fold was named perform only a small fraction of the activities included in this superfamily. Activities carried out by superfamily members include class B beta-lactamases which can catalyze the hydrolysis of a wide range of beta-lactam antibiotics, hydroxyacylglutathione hydrolases (also called glyoxalase II) which hydrolyze S-d-lactoylglutathione to d-lactate in the second step of the glycoxlase system, AHL lactonases which catalyze the hydrolysis and opening of the homoserine lactone rings of acyl homoserine lactones (AHLs), persulfide dioxygenase which catalyze the oxidation of glutathione persulfide to glutathione and persulfite in the mitochondria, flavodiiron proteins which catalyze the reduction of oxygen and/or nitric oxide to water or nitrous oxide respectively, cleavage and polyadenylation specificity factors such as the Int9 and Int11 subunits of Integrator, Sdsa1-like and AtsA-like arylsulfatases, 5'-exonucleases human SNM1A and yeast Pso2p, ribonuclease J which has both 5'-3' exoribonucleolytic and endonucleolytic activity and ribonuclease Z which catalyzes the endonucleolytic removal of the 3' extension of the majority of tRNA precursors, cyclic nucleotide phosphodiesterases which decompose cyclic adenosine and guanosine 3', 5'-monophosphate (cAMP and cGMP) respectively, insecticide hydrolases, and proteins required for natural transformation competence. The diversity of biological roles is reflected in variations in the active site metallo-chemistry, for example classical members of the superfamily are di-, or less commonly mono-, zinc-ion-dependent hydrolases, human persulfide dioxygenase ETHE1 is a mono-iron binding member of the superfamily; Arabidopsis thaliana hydroxyacylglutathione hydrolases incorporates iron, manganese, and zinc in its dinuclear metal binding site, and flavodiiron proteins contains a diiron site.	2.40718e-70
NZ_LN831776.1|WP_020426845.1|6899135_6900443_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	8.88202e-67
NZ_LN831776.1|WP_039786342.1|6897335_6898055_-|pirin-family-protein	gnl|CDD|380375	cd02910, cupin_Yhhw_N, Escherichia coli YhhW and YhaK and related proteins, pirin-like bicupin, N-terminal cupin domain. This family includes the N-terminal cupin domains of YhhW and YhaK, Escherichia coli pirin-like proteins with unknown function. YhhW is structurally similar not only to human pirin but also to quercitin 2,3-dioxygenase (quercitinase). Although the function of YhhW is not completely understood, YhhW and its human ortholog have quercitinase activity and are likely to play an important role in transcription and apoptosis. This N-terminal cupin domain of YhhW has a metal coordination site and is thought to have catalytic activity while the C-terminal cupin-like domain has diverged considerably and has closer alignment with C-terminal pirin. YhaK is found in low abundance in the cytosol of E. coli and is strongly up-regulated by nitroso-glutathione (GSNO). There are major structural differences at the N-terminus of YhaK compared with YhhW; YhaK lacks the canonical cupin metal-binding residues of pirins and may be involved in chloride binding and/or sensing of oxidative stress in enterobacteria. YhaK showed no quercetinase and peroxidase activity; however, reduced YhaK was very sensitive to reactive oxygen species (ROS). Proteins in this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold.	9.02959e-57
NZ_LN831776.1|WP_046505765.1|6884910_6885477_-|thioredoxin-family-protein	gnl|CDD|379658	pfam14595, Thioredoxin_9, Thioredoxin.	1.51426e-49
NZ_LN831776.1|WP_020426840.1|6895435_6896221_-|alpha/beta-fold-hydrolase	gnl|CDD|131480	TIGR02427, b-ketoadipate_enol-lactone_hydrolase, 3-oxoadipate enol-lactonase. Members of this family are 3-oxoadipate enol-lactonase. Note that the substrate is known as 3-oxoadipate enol-lactone, 2-oxo-2,3-dihydrofuran-5-acetate, 4,5-Dihydro-5-oxofuran-2-acetate, and 5-oxo-4,5-dihydrofuran-2-acetate. The enzyme the catalyzes the fourth step in the protocatechuate degradation to beta-ketoadipate and then to succinyl-CoA and acetyl-CoA. 4-hydroxybenzoate, 3-hydroxybenzoate, and vanillate all can be converted in one step to protocatechuate. This enzyme also acts in catechol degradation. In genomes that catabolize both catechol and protocatechuate, two forms of this enzyme may be found. All members of the seed alignment for this model were chosen from within protocatechuate degradation operons of at least three genes of the pathway, from genomes with the complete pathway through beta-ketoadipate. [Energy metabolism, Other].	1.89006e-37
NZ_LN831776.1|WP_020426849.1|6904174_6904678_+|YtxH-domain-containing-protein	gnl|CDD|378938	pfam12732, YtxH, YtxH-like protein. This family of proteins is found in bacteria. Proteins in this family are typically between 100 and 143 amino acids in length. The N-terminal region is the most conserved. Proteins is this family are functionally uncharacterized.	9.30906e-14
NZ_LN831776.1|WP_020426030.1|6890521_6891715_-|SAM-dependent-methyltransferase	gnl|CDD|379330	pfam13679, Methyltransf_32, Methyltransferase domain. This family appears to be a methyltransferase domain.	1.57051e-50
NZ_LN831776.1|WP_020426280.1|6886751_6887405_+|SdpI-family-protein	gnl|CDD|379303	pfam13630, SdpI, SdpI/YfhL protein family. This family of proteins includes the SdpI and YfhL proteins from B. subtilis. The SdpI protein is a multipass integral membrane protein that protects toxin-producing cells from being killed. Killing is mediated by the exported toxic protein SdpC an extracellular protein that induces the synthesis of an immunity protein.	2.41847e-16
NZ_LN831776.1|WP_081487115.1|6896326_6896905_-|spore-protease-YyaC	gnl|CDD|131888	TIGR02841, Uncharacterized_protein_YyaC, putative sporulation protein YyaC. A comparative genome analysis of all sequenced genomes of shows a number of proteins conserved strictly among the endospore-forming subset of the Firmicutes. This protein, also called YyaC, is a member of that panel and is otherwise uncharacterized. The second round of PSI-BLAST shows many similarities to the germination protease GPR, which is found in exactly the same set of organisms and has a known role in the sporulation/germination process. [Cellular processes, Sporulation and germination].	1.82293e-42
NZ_LN831776.1|WP_052741532.1|6887707_6890377_-|hypothetical-protein	gnl|CDD|225844	COG3307, RfaL, Lipid A core - O-antigen ligase and related enzymes [Cell envelope biogenesis, outer membrane].	1.87514e-10
NZ_LN831776.1|WP_020426028.1|6892994_6893498_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|378968	pfam12840, HTH_20, Helix-turn-helix domain. This domain represents a DNA-binding Helix-turn-helix domain found in transcriptional regulatory proteins.	4.08265e-09
NZ_LN831776.1|WP_020426844.1|6898302_6899139_-|sugar-ABC-transporter-permease	gnl|CDD|226354	COG3833, MalG, ABC-type maltose transport systems, permease component [Carbohydrate transport and metabolism].	3.94983e-104
NZ_LN831776.1|WP_020426842.1|6897017_6897242_+|DUF1128-domain-containing-protein	gnl|CDD|377674	pfam06569, DUF1128, Protein of unknown function (DUF1128). This family consists of several short, hypothetical bacterial proteins of unknown function.	3.46916e-27

Protein sequences

>NZ_LN831776.1|WP_167345705.1|6893503_6894796_+|MFS-transporter
MPASTSESGKTNPFRGFAAPFAKSRAFPFLWLGHLISFLGSSVTMVILPVLVYSLTGSTTTMGVVMAVYMLPNILMLPVSGHIVDRYDRVGIMMLADIFRALIMLATAVLALTGLLSIPLLLILIGCYGLLDGLFQPAYAAVRATVFTPDIRVTANSVTQITTQTVRLIGPALGGLLITHLSAGIGFGLDAFTYVFSFICLIYLRRALIARVRTDASGTAGSMAAPSPSADWKQDFMEGLAVLRSHPWLWITILAFSFINICYGGITSILVPWLFKVQHGWDPYLYGLAVTCSGAGAILAGLIFGTRQRWSRRGLMAYGGAFISGVSLLLLPFVPSAAGAVILFSLEGFGLMVFMLIWEISMQELVPQEAFGRVASLDLLGSFALLPVGYILVGWLADLIGGVATIAIFSGLGMACIALVLSIPAIRNFQ
>NZ_LN831776.1|WP_020426028.1|6892994_6893498_+|helix-turn-helix-transcriptional-regulator
MNEDKEYQASIQRQPLKVSPEQEKLLESALRIKIMHLLAAEPLTSKQVAEKLEKTPGNVHYHISKLFEGGLLELVRTEAAGGIIQKFYRSKATWFRAENFSGFQFRAEDQVDHFTTRLTLSPEELESFRREMMDFISSWESRVTLGTEYGVDIVIGHLRTPEPEVNP
>NZ_LN831776.1|WP_020426029.1|6892068_6892731_-|hypothetical-protein
MFRRDYIVRMIEDMTAMVAKVMTLKQEKKTTEALWEVDELLIRHFRLNSRLLNSLSVEDIIDMYLLGGVVESDKLQGVARLLKEEGAIYTAAGDKDAGLFRAMRSLHLFLYADLHGADRTLLQMPADIDELLRETQAYSLPAKTERLLLSYMESLGRYAKAEDSLYRLWEQGEDVVQEGKELYSRLLLKSPEELELGGLPEQEVRDGLKEWERRTAAVRQ
>NZ_LN831776.1|WP_020426030.1|6890521_6891715_-|SAM-dependent-methyltransferase
MYPVESLNALIEQVMSGRTLITATLSQLRSKGETTYTKVQVKPVELKGKLHYQFAYYTGPKVEHRNIPAESAAAELMSLFREKFRQGLLCTVEADYQVLISKKYKVSILTKSPSKQEAPNLDHNRRKRYVLDEGEPVPFLVELGIMNSEGKVLAKKYDKFRQINRFLEMVEDVLADLPTGRPLTIVDFGCGKSYLTFALYHYLAIREQRELNIVGLDLKADVIEHCSALAAKLGYGKLRFLVGDIADYNELEQVDMVVTLHACDTATDAALEKAVRWGASVILSVPCCQHELFAQIESGVLNPLLSHGILKERFSALATDAIRAKLLDLMGYRTQLLEFIDMEHTPKNILIRAVKGASGDNAAKWREYSAFRDFLGAKPYLERVCTDLLPGESTVQG
>NZ_LN831776.1|WP_052741532.1|6887707_6890377_-|hypothetical-protein
MRLNNQDSQKKALVFACTGAVFAAVMAASLLRGMFFAGEIYPFLTVWLVLCGIFCAWGQAVSASRNDEGRDHVLKIAVVNKPALILLGCPLAIFVLYAWAGLRGPVSAQDTADELLRWAFYATFALLAYFCAADRQGARLLAAIWHVTGMTLSLSALLAVCAQLKLPYAVAYTAAPEVSATGARLAGLLQYPNTFGVVMAVFLLERLFAAAVHVQRAQSRAAERGAGTKERSGKNGTSGREGTRKGRKREAAQGIRERSGKTGTSVWRNMRRERGNAHRIIEWEWSGEKGISGSRNMQRERGVAHRIIEWEQSGKKRIRKLSGLCSSAGGRQLLRMLPLFPCAAALLLSESRGAWLAAALASAAALLWKRQLCMPLLLAGAAPVAAAAWLYRQLARTGLAVEPVSGLLLLAGLWGAALLGGAWLCRRRTGAAGGWHAARAALAAALWTAAGSAVLLQVSERITGPSSTVAARGLFYRDAWKLAAEAPWLGRGGGTWRSTYLAAQSRPYVGSQVHSGYLDLLLNLGGVGLAVILLLLLAAGWLVAAGAPRLLPPLLALALHSAVDFDWSYGLVWLLLLLLPALARAEKLHHAATDNLPVRDIAVKSLPITGGPGSLAAEPGLAPAAPLPLHAAPAGAADNSPVRLVSAKSPPITGDPWRLVPFAVQHPLLRVSLVTLLCGVTLALSVLSFQMMKGESLYKQAAGASHREERISLLRQSLQWNPRQPKAAAALSRMLPEPEGSALLRKALGYAPEDAALNWELAKRAMRGKHPGTALYRVRKGEALDVFNVVKRVEAAEGMLDMSVRKLKDGDELGALQSADAGLELLREYRLLIEQEGSKGLQHNDRRFGAQKEAEGIDLRLTEARAAACYLRTAMLPVSGEGTEPEVEP
>NZ_LN831776.1|WP_020426280.1|6886751_6887405_+|SdpI-family-protein
MKDFKWKWQDTVIVILGVLSLGYALANYGKLPDQLPAHFDIRGEADRYWSKGSVIAFTGFLGLIFPLAMQFIKSVDPKKENYSKFQNAYKMIRLAIAALFDAMLVLTVSYGLNQNIPAGKIAMVAIGLLFIVVGNFMPQIRDNYFTGIRTAWTLASPEVWRKTHRFSGVMWMIGGLLIALGAFLPQSLSISMIIAALVIAIILPFAYSWLISSRTKA
>NZ_LN831776.1|WP_020426278.1|6885473_6886088_-|DedA-family-protein
MHVISDLISHLFEWIQSLGYFGIMIGLMIEVIPSEIVLAFGGYLVSQGEINYFGAVLFGTVGGVIAQIFVYWIGRYGGRPVLEKYGKYIFIKKKHIDHSEEWFNKYGTGVIFTARFIPVVRHAISVPAGISRMPLGKFTLLTTLAVIPWSALFVYLGYTLGDKWETIDEVAAKYTHELILAAIAIIVIYFLFKWYKSKKKGSAV
>NZ_LN831776.1|WP_046505765.1|6884910_6885477_-|thioredoxin-family-protein
MKQNVAHKFGQGLTPRQFVEGMTKNQQAFESWYEKFAWEDQDDRAYFESLNHRDDLRVLILAADWCGDVVRNVPVVFRILETAGIKTEVLILEENQDVMDDFLTMGGRSVPIVIFADTGGYVLGHWGPRPEHVQSLMREFKRENPDREAPDYESKIAEVRKAMGQAYGEGTESHAVIAKELRSLISGF
>NZ_LN831776.1|WP_020426276.1|6884274_6884904_-|MBL-fold-metallo-hydrolase
MLNIRSYNLGPLQTNAYLLTGADPGRGVIIDPGANPAALLRAAQEMEIEAVLLTHAHFDHIAGLDEIRRAKKCPVYLHTLESEWLGSPKLNGSLMWPDVTPPISTEPAEYDLADGQVLNLLGLTFRVMHTPGHSPGSVSFLCGSDLFSGDVLFKLGVGRTDLTGGRERDLIDSIRNKLYRLDEEVRVFPGHGPRTTIGFERQCNPYVPM
>NZ_LN831776.1|WP_020426275.1|6883909_6884086_-|hypothetical-protein
MKDTEEEVHEEEAHKAPISTTGGQDKKECLFWSFPHGKGAIQPWRRRLWELQNNSDRE
>NZ_LN831776.1|WP_020426840.1|6895435_6896221_-|alpha/beta-fold-hydrolase
MEIVRCEGSNICYSDQGTGDVIVLLHGFCGSSSYWEQVIPLLSGNYRVIAPDLRGHGVSDAPLGAYSIDQMADDVLSLLDALEIPECYLLGHSLGGYITLSFAQRHASRLKGFGLIHSTGYPDSGEARENRLKSVSMIQNEGIFAFVDGLVPGLFAPGAAPQLLERTKEIGYRTPPQGAVGAAMAMRERPDRRDVISATALPVLLVAGAEDSKVTPEQTFTSNKPNVTQATISGVGHMSMYEAPERLAEIIKDYVHAAVRK
>NZ_LN831776.1|WP_081487115.1|6896326_6896905_-|spore-protease-YyaC
MCHKKQKEARTLAIREQESRKRKKRDASGLIFFFREIASQHPPEQITFLCIGTDRSTGDALGPLTGSQLLEQGFPHVSGTMPSPCDADNLEARIAEIPAGQIVIAVDACLGPPASLGYFLTADEPLRPAQSVGLNLPAVGHYSLAAIVDVYGPRPYRTLQSTPLHRVMVMAKQIALAAAAGFGMETGKAFQD
>NZ_LN831776.1|WP_020426842.1|6897017_6897242_+|DUF1128-domain-containing-protein
MDLSQPTQENVEYMIEGIKSKLKMASAAAMQASAFSVKNYEDILDIYEVAMGSDRLSISQVEALVSELGRLRDK
>NZ_LN831776.1|WP_039786342.1|6897335_6898055_-|pirin-family-protein
MIKVITSAERHTSNREWIHSEFSFSFADYDDPSNAHFGALLAHNDNELSPGQGMHEHPHHDLEIITYVVSGVLKHQDDLGNHAELQGGSVQVMSAGTGINHSETNPSDSEHVRFLQIWLLPDQPGRQPKWDAKFYPAEHKTNTLLPVASGKGEEGALEIHENVTVYLSSLERSRELKYQQREDRRTHIYLISGHLEIACSDGVFQLEPGDAARIRKSCDLHLKGTGSDSNAEFILIDLP
>NZ_LN831776.1|WP_020426844.1|6898302_6899139_-|sugar-ABC-transporter-permease
MNRKPEEAAKTIGSYALLILLSFISLFPAFWIVMSSFKTGNSLFSDTLIPRRMTLVHYQELFEQTKYLQWFLNTLKVAALSTLIGTSLLLLASYAISRYRFAGRKSMLTAFLVLQMFPGFMAMIAIYVLLNTLGLLNSHWALVLVYSSGSIITNVFVAKGFFDTIPKSLEDAARIDGASHMKVFLSIMMPLSKPMLTYASLMIFNGCFVDFIFADLILRTEEKRTLAVGLFRMVNQSNSTEFTLFAAGAVLVALPVTLLFIFLQRFLIDGLTAGAMKG
>NZ_LN831776.1|WP_020426845.1|6899135_6900443_-|sugar-ABC-transporter-permease
MPKKTGAAVLSAVIPGLGQMYNRQWLKGLAFLLTGMAWFYFMTHGLTGHLRGLITLGELPSRMVKVGKMTRMVEGDHSIFMMINGLMALLALLLYCGFYLLNIRDAFMVGAARARQEQIRSFGQSLKYMGRRHFAYLVLAIPLTAIVFLTILPLVFSVLLAFTNYADPILPPANLVDWVGFGNFKKMLSLDVWSTTFGGILTWTLCWAVIATVTTYIGGVLVAVLIHQPRVRFKKLWRTLLIVPFAIPNMISLLVMRNMFNNQFGPVNKYLGMIGLNGLPWLTDPFWAKVTVILANMWIGIPVTMILAFGVLTTIPRDLYEAAEVDGAGSAHKFRMITLPMVLFATAPILIMQFAGNINSFNVIYLMTNGEPVNPHYQYAGDTDLLVTWLYKLALNQSQYSFASVIGIIIFLLVATFSIWSYRRTRSYKEEDMIT
>NZ_LN831776.1|WP_039786345.1|6900462_6901761_-|maltose-ABC-transporter-substrate-binding-protein
MNAVSKIVVLCMLLVMTATACSSNSPNTAPSPKGGNNQTAETSAPENTADPEMEPEQGAKLMVWEAKEQLEYMKGVAADFEKKYGVPVNVEELAGGDQGGRLATDGPAKLAADVLTLPHDQISQAVKAGLLLPNDVFEEETKASMVETAVQASSYDGVLYGYPKSVETYALFYNKDLVPEAPKTWNDIIAFANTYNKPKENKFAIMWEFVGYYTYPFIGSFGGYIFGDSNSNPKDIGLNNEGTIKGFTFLQSLKKILPLNAGDITFDVKTQLFQEGKLAMNIDGPWSTGSFKDHVNFGVVPLPKGPNGEEMISFSGVKSYYVNSYTAYPVAARLFAHFASSKDNQLKNYKMTGAIPASIEAGESQEIKNDPITLGFFEQFQHSVPMPAISEINAVWEPLKAAFVSLWNDPGLDVKQTMDQTVKTIQSDLESK
>NZ_LN831776.1|WP_020426848.1|6902237_6903989_+|alpha-glycosidase
MIHLESVYHRMGQNWSYAYDETVIHIRLRTKRDDVSRVDLICGDKYGWDRTHSEYAMERLSSDNLFDYWQAAVRPPHRRLAYYFALHQDGNTVYFLEKGFLEHPPEIIYEGLFDFPILSPEDVHQPPAWVKDAVFYQIFPERFANGDPSNDPEGVLEWGGTPSPTNFFGGDLQGVLEHLDYLCALGINAIYFNPLFAATTNHKYDTADYLRIDPHFGTNELLKELVDACHAKGIRVLLDGVFNHCGHTFPPFMDVLENGRASRYADWFHVKEWPPVVNGGIPTYDTFAFEPIMPKFNTANPEVKEYLLKVGRYWIEEIGVDGWRLDVANEVSHQFWRDFRTMVKQINPDAYLVGEIMHDSLPWLLGDQFDAVMNYQLTNMLLNFFARGQTSAGQFSRSVGTLLANYPQQITEVSFNLLDSHDTVRFLTLCGGDIRRLKLAFLFLMTYQGTPCIYYGDEIGMDGEYDPHNRKCMEWEPRKQNQDLLEYYRWAIRLRKANSAFRSSAIKFLEHPEHPELLVYERWDEHDRFLVIMNNSELPIDAHISALKPESTWINLELQQPADIGERGQLQLPAYGYVILRET
>NZ_LN831776.1|WP_020426849.1|6904174_6904678_+|YtxH-domain-containing-protein
MNKAETEYPVESGSTFFKGVFIGGLIGAAAALLFAPKPGREMRSDLSEKFSTATDKTKEVAGVVTDKTKSIAATVGEKATDLASTVSAKASDIFTTVNDSKQQIAATLSETGKKIGDTVGSASADVASDVKDASKDVAEEASASSKDIADTANDAKEEVKASYKSSY
>NZ_LN831776.1|WP_020426850.1|6904831_6905164_+|hypothetical-protein
MGDAGSNTKRYEVEEHPFELRHEVKRLNARLDKIADSLEKSEFKDILENYTNPKKRIITNLMAGISRGLGLSLGTFVILGLLGYILSLFLNVPVIGEYLGEIKKYIDANS

Crispr_ID: NZ_LN831776_68

• CRISPR_ID: NZ_LN831776_68
• CRISPR_location: 6935548-6935622
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_68

Consensus_repeat	Method
ATGTGGAAAAAGGGACACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_68

>68.1|6935571|29|NZ_LN831776|CRISPRCasFinder
TGCCGGAGTACCCTATCCTCGGGCAGATG

CRISPR arrays and Neighbor proteins around NZ_LN831776_68

CRISPR arrays

The CRISPR arrays of NZ_LN831776_68

>merge|NZ_LN831776|68|6935548-6935622|CRISPRCasFinder
ATGTGGAAAAAGGGACACTAATTTGCCGGAGTACCCTATCCTCGGGCAGATGAAGTGGAAAAAGGGACACTAATT

>NZ_LN831776|68|68|6935548-6935622|CRISPRCasFinder
ATGTGGAAAAAGGGACACTAATT	TGCCGGAGTACCCTATCCTCGGGCAGATG
AAGTGGAAAAAGGGACACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_046505782.1|6933462_6934371_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_020426867.1|6920136_6921762_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|237894
NZ_LN831776.1|WP_039786316.1|6931576_6933295_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270300
NZ_LN831776.1|WP_020426829.1|6944039_6944234_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426831.1|6945665_6945899_-|glutaredoxin-family-protein	unknown	unknown	gnl|CDD|239274
NZ_LN831776.1|WP_020426832.1|6946054_6946996_-|thioredoxin-disulfide-reductase	unknown	unknown	gnl|CDD|273540
NZ_LN831776.1|WP_020426824.1|6935843_6937397_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_020426825.1|6937393_6939178_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_020426828.1|6942748_6943909_+|ROK-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224851
NZ_LN831776.1|WP_167345678.1|6944354_6944516_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_039786312.1|6927668_6928805_-|transglutaminase	unknown	unknown	gnl|CDD|227604
NZ_LN831776.1|WP_020426827.1|6941024_6942344_-|xylose-isomerase	unknown	unknown	gnl|CDD|235487
NZ_LN831776.1|WP_020426830.1|6945084_6945525_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379228
NZ_LN831776.1|WP_020426866.1|6919849_6920035_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426869.1|6923113_6924247_+|hypothetical-protein	unknown	unknown	gnl|CDD|379361
NZ_LN831776.1|WP_046507587.1|6924762_6926190_+|amino-acid-permease	unknown	unknown	gnl|CDD|182767
NZ_LN831776.1|WP_046505779.1|6929051_6931436_-|glycoside-hydrolase-family-95-protein	unknown	unknown	gnl|CDD|379625
NZ_LN831776.1|WP_020426826.1|6939338_6940835_-|xylulokinase	unknown	unknown	gnl|CDD|198374
NZ_LN831776.1|WP_020426868.1|6921881_6922871_-|hypothetical-protein	unknown	unknown	gnl|CDD|293841
NZ_LN831776.1|WP_020426823.1|6934433_6935414_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_046505782.1|6933462_6934371_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	3.14941e-60
NZ_LN831776.1|WP_020426867.1|6920136_6921762_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|237894	PRK15064, PRK15064, ABC transporter ATP-binding protein; Provisional.	0
NZ_LN831776.1|WP_039786316.1|6931576_6933295_-|extracellular-solute-binding-protein	gnl|CDD|270300	cd13582, PBP2_AlgQ_like_3, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	0
NZ_LN831776.1|WP_020426831.1|6945665_6945899_-|glutaredoxin-family-protein	gnl|CDD|239274	cd02976, NrdH, NrdH-redoxin (NrdH) family; NrdH is a small monomeric protein with a conserved redox active CXXC motif within a TRX fold, characterized by a glutaredoxin (GRX)-like sequence and TRX-like activity profile. In vitro, it displays protein disulfide reductase activity that is dependent on TRX reductase, not glutathione (GSH). It is part of the NrdHIEF operon, where NrdEF codes for class Ib ribonucleotide reductase (RNR-Ib), an efficient enzyme at low oxygen levels. Under these conditions when GSH is mostly conjugated to spermidine, NrdH can still function and act as a hydrogen donor for RNR-Ib. It has been suggested that the NrdHEF system may be the oldest RNR reducing system, capable of functioning in a microaerophilic environment, where GSH was not yet available. NrdH from Corynebacterium ammoniagenes can form domain-swapped dimers, although it is unknown if this happens in vivo. Domain-swapped dimerization, which results in the blocking of the TRX reductase binding site, could be a mechanism for regulating the oxidation state of the protein.	1.00436e-22
NZ_LN831776.1|WP_020426832.1|6946054_6946996_-|thioredoxin-disulfide-reductase	gnl|CDD|273540	TIGR01292, Thioredoxin_reductase, thioredoxin-disulfide reductase. This model describes thioredoxin-disulfide reductase, a member of the pyridine nucleotide-disulphide oxidoreductases (pfam00070). [Energy metabolism, Electron transport].	4.35858e-159
NZ_LN831776.1|WP_020426824.1|6935843_6937397_-|response-regulator-transcription-factor	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	4.1481e-55
NZ_LN831776.1|WP_020426828.1|6942748_6943909_+|ROK-family-transcriptional-regulator	gnl|CDD|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	3.99567e-66
NZ_LN831776.1|WP_039786312.1|6927668_6928805_-|transglutaminase	gnl|CDD|227604	COG5279, CYK3, Uncharacterized protein involved in cytokinesis, contains TGc (transglutaminase/protease-like) domain [Cell division and chromosome partitioning].	1.01549e-21
NZ_LN831776.1|WP_020426827.1|6941024_6942344_-|xylose-isomerase	gnl|CDD|235487	PRK05474, PRK05474, xylose isomerase; Provisional.	0
NZ_LN831776.1|WP_020426830.1|6945084_6945525_-|GNAT-family-N-acetyltransferase	gnl|CDD|379228	pfam13508, Acetyltransf_7, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.19109e-07
NZ_LN831776.1|WP_020426869.1|6923113_6924247_+|hypothetical-protein	gnl|CDD|379361	pfam13769, Virulence_fact, Virulence factor. This domain is found in conserved virulence factors. It is often found in association with pfam02985 and pfam08712.	2.21651e-28
NZ_LN831776.1|WP_046507587.1|6924762_6926190_+|amino-acid-permease	gnl|CDD|182767	PRK10836, PRK10836, lysine transporter; Provisional.	0
NZ_LN831776.1|WP_020426823.1|6934433_6935414_-|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	1.36738e-133
NZ_LN831776.1|WP_046505779.1|6929051_6931436_-|glycoside-hydrolase-family-95-protein	gnl|CDD|379625	pfam14498, Glyco_hyd_65N_2, Glycosyl hydrolase family 65, N-terminal domain. This domain represents a domain found to the N-terminus of the glycosyl hydrolase 65 family catalytic domain.	1.4841e-82
NZ_LN831776.1|WP_020426826.1|6939338_6940835_-|xylulokinase	gnl|CDD|198374	cd07808, FGGY_D-XK_EcXK-like, Escherichia coli xylulokinase-like D-xylulose kinases; a subgroup of the FGGY family of carbohydrate kinases. This subgroup is predominantly composed of bacterial D-xylulose kinases (XK, also known as xylulokinase; EC 2.7.1.17), which catalyze the rate-limiting step in the ATP-dependent phosphorylation of D-xylulose to produce D-xylulose 5-phosphate (X5P) and ADP. D-xylulose has been used as a source of carbon and energy by a variety of microorganisms. Some uncharacterized sequences are also included in this subgroup. The prototypical member of this CD is Escherichia coli xylulokinase (EcXK), which exists as a dimer. Each monomer consists of two large domains separated by an open cleft that forms an active site. This model includes both the N-terminal domain, which adopts a ribonuclease H-like fold, and the structurally related C-terminal domain. The presence of Mg2+ or Mn2+ is required for catalytic activity. Members of this subgroup belong to the FGGY family of carbohydrate kinases.	0
NZ_LN831776.1|WP_020426868.1|6921881_6922871_-|hypothetical-protein	gnl|CDD|293841	cd16283, RomA-like_MBL-fold, Enterobacter cloacae RomA and related proteins; MBL-fold metallo hydrolase domain. Derepression of the romA-ramA locus results in a multidrug-resistance phenotype. Members of this subgroup belong to the MBL-fold metallo-hydrolase superfamily which is comprised mainly of hydrolytic enzymes which carry out a variety of biological functions. The class B metal beta-lactamases (MBLs) from which this fold was named are only a small fraction of the activities which are included in this superfamily. Activities carried out by superfamily members include class B beta-lactamases, hydroxyacylglutathione hydrolases, AHL (acyl homoserine lactone) lactonases, persulfide dioxygenases, flavodiiron proteins, cleavage and polyadenylation specificity factors such as the Int9 and Int11 subunits of Integrator, Sdsa1-like and AtsA-like arylsulfatases, 5'-exonucleases human SNM1A and yeast Pso2p, ribonuclease J and ribonuclease Z, cyclic nucleotide phosphodiesterases, insecticide hydrolases, and proteins required for natural transformation competence. Classical members of the superfamily are di-, or less commonly mono-, zinc-ion-dependent hydrolases, however the diversity of biological roles is reflected in variations in the active site metallo-chemistry.	1.82325e-86
NZ_LN831776.1|WP_020426825.1|6937393_6939178_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	4.12402e-63

Protein sequences

>NZ_LN831776.1|WP_020426823.1|6934433_6935414_-|sugar-ABC-transporter-permease
MKADTATAPIPPDTRKRNKKPASGGRFWRNFKNQKYLWMMSIPFVIWAFVFSYLPLWGWTMAFQKYKPARGFFEQEWVGFDHFKTLFSDSQFLLALRNTLAMSGMGLVAGFIFPITFAILLNEVRLGIFKRFAQTVSYLPHFVSWVVAAGIVTKMLSSENGLVNDILLGIGFIDSPIQFMAQGHLFWGIVTLSDVWKETGWNAIIYLAAISGIGPELYEASRVDGASRLRQVWHITLPGIRPTIIVLLIMSIGNLLNIGFEKQFLLQNNLVTDYSQVLDLYSLKYGLGMARYSYGTAINIFNSVISVILLFTINGIFKRTTKESLL
>NZ_LN831776.1|WP_046505782.1|6933462_6934371_-|carbohydrate-ABC-transporter-permease
MVGNTALTGKSWADRIFDFIVYLVVLIVIVVTIYPFLNVLAISLNDSVDSVRGGITIYPREFTWDNYLKIFTFSGLVTGFKISALRTVAGTLLGLISASMLAFTVSRPDFQGRKFVSTFLAMTMYISGGMIPVYMLVKDLGMMNSFAVYIVPGLVSAFNVFVIRSFIDGLPYALQESAKLDGANDFTIYLRVILPLLKPALATISLFLAVGQWNAWFDTYLYNGSSPHLTTLQYELMKVLQTTTSGNNGDYRSNIASMASNQVSPESLKMAITIVVTVPILMVYPFIQKYFVKGMTLGAVKS
>NZ_LN831776.1|WP_039786316.1|6931576_6933295_-|extracellular-solute-binding-protein
MKAKASAITLTSVMLLGLLAGCGGNNGNNAAGNAANTGNNANKAEDTSPLTMTYFSADPNPNWTGMQDEVGKVLTEKTGVTLEAEFAVGDPQQKVALIAASGEYPDLISAKTDISKLVDAGAMLDLTDLIDKYAPNIKKVLGEEGLKRSRYSDDDHAIYAIPTYAGVDNKYFDAGGGFELQHRAVKEAGYPEIKTVQDYENVIKAYLEKHPTDENGNKNIGMTLNADDWYMYITVTNPAFITTGSPDDGEYAIDIDTQEVTYHFRRPAEKEYFRWLNHMNDIGLLDPESFVQKYDQYKAKIATGRVIGLIDQDWGYGDGEKALKAAGKLDQGYAHFPVTLSEEYKDTSFWPTGFMAGNGVGISVDAKDPVRAIKFLDYLASDEGQVLINWGIEGKHYNVVDGKRVIPEDVNNRKYNDTTNFQKETGLGNVGSSYALLSAHYGDGVLDPTGSYYTTRFPEQVTAGYNKVEKETLAAYKANTWKDLFPSEDEFKVKPWGAAWNITIPGDSEIVVLDNKLKDITWKRIPEAILSKPADFDKVWDAYMGELDKAGVSKAEDLREELVKKRVKLWNE
>NZ_LN831776.1|WP_046505779.1|6929051_6931436_-|glycoside-hydrolase-family-95-protein
MYVGESRNTGRHKLWYNRPAAVWEEALPVGNGRLGGMIFGGVEEELIQLNEDTLWSGFPRDTTNYEALRHLAPAKQLVAEGKYKEAEALIDAKMLGRRTESYQPLGDLKIRFDLAGPVEDYRRELDLEQALAAVSYTAGGVKIVREVLASRPDELIAIHIRAEGRGELNVLPDFTAELSSPHPSCFRMTPDGTLIMTGRAPSHVADNYTGDHPRSVLYEEGLGISYAAALEIRTDGGTCTAENGSLSVSGANAVTLRLAAATDFAGYDKMPGRGGTVPSELCLKQLASASQAYAELRLHHIRDHQTLFRRVSLELAPASSLAELPTDDRLAQYREGQADPALEVLLFQYGRYLMIAGSRPGTQALNLQGIWNPHVQPPWNSNYTTNINAEMNYWPAEPCGLGECHEPLMDLITELSLAGRRTANIHYGARGWSVHHNTDLWRMTTPSDGLSMWAFWPMGGVWLSRHLWERYAFRPDRAFLQDTAFPVLKGAALFCLDFLVELPDGRLTTGLSTSPENVFLTADGEPCSVSAGSAMDMSLIAELFSHCIQAAEILDTEPEFRRELTAKRARLAHPGIAPDGRIREWHRDFAEKEPGHRHVSHLYGLYPGNVISPDQTPELAAAAALSLETRLESGGGHTGWSASWLLNLYARLQDGEKAYRCVQRILEAATLPNLFGNHPPFQIDGNFGVAAGIAEMLLQSHQNGLQLLPALPGSWSGGRVSGLRARGGFIVDMEWSGGQLVRAVLVSTHGYPCSVSGSLPLTLQKPDGALSDAGAVFETIAGETYILIPQHKKN
>NZ_LN831776.1|WP_039786312.1|6927668_6928805_-|transglutaminase
MKKRYTLVKAMLGGMLVCAALPPALYWGWDHAYAASTSAVLQSGAEMAQKLTAAMNNRRENITFVYEGKTTNLKSQVQKAIDQAMGSDPYLYYIIDSYAFSYRGSSRSAKVTVQVAYRETLQQTALVNKQVKTLLQQIITPGMNQHQKVKVIHDWVVLHLQYDNTYRKYTAYEGLQTGSAVCQGYSLLTYKLLLGAGIPNKIVEGTAKPEGGVAQSHAWNLVQLDGRWYHLDTTWDDPTPSPEGGVSTVYYMRTDAQMRRDHSWTKSYPAASVGYAQTLSELVSRGGQSVPVYQELQKKLDYRLYEEDEVITSAAELNTLVREAAASGKQSLLFRYRGSEKLLKIDLQGLYSLGLENLAYTSSPFDNTGDLKVYVTWK
>NZ_LN831776.1|WP_046507587.1|6924762_6926190_+|amino-acid-permease
MRKTFKARHLTMIALGGSIGTGLFLASGGAIASSGPGGALLAYTAVGIMVYFLMTSLGELATYLPDSGSFSTYGTRFVSPAFGFAIGWNFWYNWAVTIAAELSAATVIIKYWFPDSPSILWSLLFLLLMFGLNFLSARGYGESEYWFAIIKIITVIVFLTVGVLMIFGILGGKAVGFSNFQLGGSSFHGGFFAFVGVFMAAGFSFQGTELVGVAAGESENPRRNVPLAIRRVFWRILIFYIFAILVIGLLIPYTNPDLLRSGIDDIGVSPFTIVFNKAGLAIAASVMNAVILSSVLSAGNSGMYASTRVLYAMAKDGMAPRALGRLNRRGVPVGALLVTTAVGMLAFLASFFGDGAVYNWLLNASGMCGFINWLGIAVCHYRFRRAFVKQGHSLEELPYRARWFPFGPIFALVLCLIAVFGQNLGAFNGGSIDWYGILVSYISLPLFLLIWFGYRWFRKSRIVPLDQCDLSTHPE
>NZ_LN831776.1|WP_020426869.1|6923113_6924247_+|hypothetical-protein
MKITFIEPTPSPNTMKLHLDETLEPGVRRTYTPESQRSAPSWAREMLTIPGVTSIYHAADFAALERKGSADWAAILREVQTRFGAEGLSADFNLEDENAGAHFGESQVFVQMFRGIPIQIRVKTGASEERIALSARFTKAVTDVASAVLIKERKLTDYGVRYGEPETIAREVEQELEAAYPQERLDSLVQQAIAHGAGGEFVEQREKKDQAELLRDLKDEDWRVRYAALEDLAPTAELLPELRAALHDPKLHIRRLAVVYLGDIRTPEAMELLYEAMADSAPAVRRTAGDTLSDIGDPAATPMMTASLTDKSKLVRWRAARFLYEVGTAEAQEALSLAVDDPEFEVGLQARMALERIASGEEAAGTVWQQMSERRRT
>NZ_LN831776.1|WP_020426868.1|6921881_6922871_-|hypothetical-protein
MARVRYNNIDNVSTDKTLKQLRQWREERRMKKKDYSYKVPNLPPKLDYLSENRLDTTVTWIGHSTFLLQYEGVNIITDPVWARRLGFEKRITPPGIPLSGIPPVDLILISHSHYDHLHLASIRKLYKAGTTLVVPVGLKRKMVRKGFVNCLEMQWWEEIKVGAVKLTFVPTQHWTRRTPFDTNTSHWGGFVLEPAEPRKHPQGDGGSRKLPPNLYFAGDSGFFPGFKEIGRRFKLHVALMPIGAYEPEWFMSSQHVTPEEAIQAFLDVGAELMIPMHFGTFRLADDTAREALDRMEQARLAQGIAGERIRTLAYGETLIVHPEERMPGP
>NZ_LN831776.1|WP_020426867.1|6920136_6921762_-|ATP-binding-cassette-domain-containing-protein
MISTSGVTLRYGKRALFEDVNIKFTPGNCYGLIGANGAGKSTFLKILSGEIEANTGEVHMTPGERLAVLKQNHFEYDEYPVLETVIMGHTRLYDIMKEKDALYAKSDFSEADGLRAGELEGEFAELNGWDAEPDAAAMLIGLGIMREMHDKKMAELSGNEKVRVLLAQALFGRPNNLLLDEPTNHLDLESIGWLENFLMDYEGTVIVVSHDRHFLNKVCTHIADIDFGKIQMYVGNYDFWYESSQLAQALQRDANKKKEDKIKELQAFIQRFSANASKSKQATSRKKQLEKITLDDIRPSNRKYPFLNFKPEREAGKQLLTISGLTKTVEGEKMLDEFSIVVNKGDKIAFVGPNSQPKSLLFDIIMGEKEADAGEYTWGVTTTQAYFPKDNSSYFDGVNLNLVEWLRQYSKDQDETFLRGFLGRMLFAGEEALKKASVLSGGEKVRCMLAKMMLNGANVLVFDEPTNHLDLESITALNNGLIDFDGTILFTSHDHQFIQTIANRIIEITPAGVIDRTMTYDEYLENPEIKEMRARMYPVEV
>NZ_LN831776.1|WP_020426866.1|6919849_6920035_+|hypothetical-protein
MSESNDKPKINLADAIRQKLEQKKQQTSARPGSTFQAGSAKPLKSQNNKKPNNQRRRTGGS
>NZ_LN831776.1|WP_020426824.1|6935843_6937397_-|response-regulator-transcription-factor
MMIKVLIVDDEPKLREGLRALIPWGQLGFTVVATAANGLQALEKYHIHDPELIVVDIRMPGMDGLELIGELRNEGSTSHVLILSGHADFDYAKRAIGYRIDGYLLKPVDEEEMISLLKELRETIDREDRFSRWNEEEPTRNRESLLRALLQPPAEESGADDPGKQAAALGLTPGRVEVVLIELLAPAHAIEEEERKIIAAVEQHFSGSGDRLFFTLPPYIGLLLKEPLQDGMRRERLIEELAGLICPCGFNFTAAAGGAVPRPEEAAESFNAARDLLRRAFFYRKGMMLTADPSGMLFPDSGEADTEQVTDAESRLLLAVETGSRAAIEPLVQAISAGLIAAGGEEQQIKDTFVRILSTVLARLEPVYPEIRNNTVKHFPPIGELYQSHYLEDLQEQSVAFLAEIAGQMTSGVKGNEIKKITELIQRRYNENLKLETLSELFSYNSAYLGKMFKNTTGEYFNTYLDKVRIEKAKEFLAQGMKVYEVAEKVGYMNSDYFNAKFRKYVGTSPSSFRKNK
>NZ_LN831776.1|WP_020426825.1|6937393_6939178_-|sensor-histidine-kinase
MFHWFVKLMNDIKIRNKLLLAFLGVTLLPVLLVGGYLTFEMRTMAFDNALEQASTNVDRVRKRTEEVIGVSQDISYRLNNDTRLKRLAVRKYESIYEVVKAYQDYTDVREYIRLYSEISNIRLYTDNSSLLNNWELINPSPAIKESEWYQRAQRYEGLVGWEYIEDERDHHKYLSLVRKIELEGSSKTGVLVINVNSNKLTSILNQESFDTMIVDDQNNIIASNRKEREGKTLADISFDTKLLGRGSGSYEAVVEGEPSQIVIDELSPQASRNALRVVSVFSIDSIVKEPNRIIRLALSVIAISVVLAFLLIFSFSSLFSRRLLHLSKHINRVGTGDFDTSLQIDGKDEIALLARQFNSMVRSIHDLMLEVQVSNEQNSLLQQKQNDIRFKMLASQINPHFLFNALESIRMEAHMKNQQEIARVVRLLGQMMRSSLEVGRSKVTLKQELDMVRCYLEIQQFRYEERLKYHFIVDPAIESLSMPPLIIQPLVENAVIHGLDNTLEGAVVTVEIRYEQEHAVFTITDNGVGITQDRLEQVRSTLETQEEQEGARIGLRNVHDRLKLSYGEKYGLTIESHPDEGTRISFRIPMEVAK
>NZ_LN831776.1|WP_020426826.1|6939338_6940835_-|xylulokinase
MKYVIGVDLGTSAVKTVLVDPQGKVAFEHSESYPLSRPQPNWSEQNPEDWVQGTLVSLRRLIEVSGVDPSQVDGISFSGQMHGLVLVDREGKVLRPAILWNDTRTTAQCRKIEQTLGSKLIGIARNRALEGFTLPKILWVQENEPEVLAQAALFLLPKDYVRYRLTGDYAMDYSDAAGTLLLDVGAKTWSAEIAEAFGLPFSLCPKLVESFDLTGTLLPEIAEASGLLPSTKVFAGGADNACGALGAGILGEGRTMCSIGTSGVVLSYESNKDLNLEGKVHFFNHGEKDAYYIMGVTLAAGYSLTWFKETFAGDKSFDELLQGVDSIPAGSGGLLFTPYIVGERTPHPDPNIRGSFIGMDAGHTLAHFTRSVLEGITFSLRESIDIVRDSGKEITEVVAIGGGAKNEAWLQMQADIFNASIIKLESEQGPAMGAAMLAAYGSGWFASLSECAEAFIRPAEVYKPNAQQAEVYNGLFHLYQQVYGQTRELNDKLAAYRK
>NZ_LN831776.1|WP_020426827.1|6941024_6942344_-|xylose-isomerase
MAYFESVGKISYEGSRSTNPYAFKFYNPKEIVAGKTMEEHLKFAMAYWHTLTAGGSDPFGAETAVRAWDKLSTLDKAKARAEAAFEFMEKMDLHYYCFHDVDIAPEGASLREFYSNIDTIVDILEQGMKASGKKLLWNTANMFTNPRYMHGAGSTCNADVYAHAAAQVKKGLEVGKRLGADNYVFWGGREGYETLLNTDMSLEQDNIARLFSMAVDYAKEIGFDGQFLIEPKPKEPTKHQYDFDAATTIAFLQKYNLDKHFKLNLEANHATLAGHTFEHELRVARINGMLGSLDANQGDPLLGWDTDEFPASIYDATLTLYEVLKNDGLGKGGINFDSKVRRPSFEPEDLFLAHISGMDIYAKGLKVAAKLLEDRVFENFIDKRYSSFTEGVGADIVSGKATLASLADYALNNENPRKNESGRQELLRATLNQYILAEQ
>NZ_LN831776.1|WP_020426828.1|6942748_6943909_+|ROK-family-transcriptional-regulator
MKVTGDQALVKKINKSIILHTIRKHSPVSRARVSEMTGLNKATVSNLVSELCGQELVTEAGPGESSGGRKPLMLHFNSMAGSVIGIELQVKQLKAVLCDLGGSTLQELDCPLEVHDLPYVLEKMKAIISELIASAPSSPYGIVGIGVGVPGMVDEHGMVLFAPNLGWEMVDLRAILEQSFAVPVTIDNEANAGAQGELNFGAARDVRHLLYISAGSGIGSGIIIGGELYKGARGYAGETGHMTIEAEGKPCSCGSRGCWELYASERTYDNPGLALPARSTTELVRYAHEGQEDTLRHFTTIGEYLGIGVTNLINSFNPELIVIGGALSEAEPWLGEPLRRVVAERTLPYHKQQLEITFSRLGSRGTMIGAGFSAVMHFLGNIRVTL
>NZ_LN831776.1|WP_020426829.1|6944039_6944234_+|hypothetical-protein
MTYVDTSDISAQMFITVLLLLLIIAPLISLGVLRLFQSRKKSGLLLIVSGIAVYALFQIIMYFI
>NZ_LN831776.1|WP_167345678.1|6944354_6944516_-|hypothetical-protein
MLRNNGRNAVVEAQTVGVLRNNGGNAVVEAQTVDVFRNNGKNAVVEALEVSLL
>NZ_LN831776.1|WP_020426830.1|6945084_6945525_-|GNAT-family-N-acetyltransferase
MLISLKNYWDRDAVERLLAECMEAGAAEIAEEVDRYLTGDSRELLGTFVNGELAGLAGIRHEPGEAIGLLHIAVQARLRGRGIGRAMIEELRRCQGNDMLRAETDLAGAGFFRKSGFVVTSLSEKDPGVERFDCVLPVSSQAEYAL
>NZ_LN831776.1|WP_020426831.1|6945665_6945899_-|glutaredoxin-family-protein
MENVIVYTSTNCPHCRQVKSFLSEKGISYEERNIEQNDDYAQQVWDMGMRAVPVTVIGDFKIVGMNKTQFDKALANV
>NZ_LN831776.1|WP_020426832.1|6946054_6946996_-|thioredoxin-disulfide-reductase
MYKSIIIGTGPAGLTAAIYLARANLNPLVIEGPQPGGQLTTTTEVENFPGFPDGIMGPELMDNMRKQAERFGAKFVTGWVNSVELGERPFKLNVEGMGALTTDTLILSTGATAKYLGIPGEQDNIGRGVSTCATCDGFFFRGKEIVVVGGGDSALEEAGFLTRFASKVTLVHRREELRASKIMQDRVRDNEKVAWSLNRTPLEVTSGDRGVNGIKVLNNVTGEEEFIEASGVFVAIGHHPNTAFLGGQITTDANGYIVTNPGTSETNIPGVFACGDVQDTRYKQAITAAGSGCMAAMDAEKYIESLEHSAVIL

Crispr_ID: NZ_LN831776_69

• CRISPR_ID: NZ_LN831776_69
• CRISPR_location: 6944700-6944773
• CRISPR_type: TypeV
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_69

Consensus_repeat	Method
AATTAAGTTCCCTTTTTCCACTT	CRISPRCasFinder

spacers of NZ_LN831776_69

>69.1|6944723|28|NZ_LN831776|CRISPRCasFinder
AAACCTCACAATTGTTGATTTTAGGGAG

CRISPR arrays and Neighbor proteins around NZ_LN831776_69

CRISPR arrays

The CRISPR arrays of NZ_LN831776_69

>merge|NZ_LN831776|69|6944700-6944773|CRISPRCasFinder
AATTAAGTTCCCTTTTTCCACTTAAACCTCACAATTGTTGATTTTAGGGAGAAATAAGTTCCCTTTTTCCACTT

>NZ_LN831776|69|69|6944700-6944773|CRISPRCasFinder
AATTAAGTTCCCTTTTTCCACTT	AAACCTCACAATTGTTGATTTTAGGGAG
AAATAAGTTCCCTTTTTCCACTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_046505782.1|6933462_6934371_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_020426839.1|6958308_6959109_+|polysaccharide-deacetylase-family-protein	unknown	unknown	gnl|CDD|200589
NZ_LN831776.1|WP_020426825.1|6937393_6939178_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_LN831776.1|WP_046505792.1|6957926_6958127_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426837.1|6956860_6957727_+|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_020426832.1|6946054_6946996_-|thioredoxin-disulfide-reductase	unknown	unknown	gnl|CDD|273540
NZ_LN831776.1|WP_020426824.1|6935843_6937397_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|381091
NZ_LN831776.1|WP_020426836.1|6956097_6956763_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426834.1|6949554_6952029_-|hypothetical-protein	unknown	unknown	gnl|CDD|225990
NZ_LN831776.1|WP_020426828.1|6942748_6943909_+|ROK-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224851
NZ_LN831776.1|WP_046505789.1|6952060_6956092_-|glycoside-hydrolase-family-2	unknown	unknown	gnl|CDD|225789
NZ_LN831776.1|WP_020426831.1|6945665_6945899_-|glutaredoxin-family-protein	unknown	unknown	gnl|CDD|239274
NZ_LN831776.1|WP_020426827.1|6941024_6942344_-|xylose-isomerase	unknown	unknown	gnl|CDD|235487
NZ_LN831776.1|WP_020426830.1|6945084_6945525_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379228
NZ_LN831776.1|WP_039786316.1|6931576_6933295_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270300
NZ_LN831776.1|WP_020426833.1|6947199_6949155_-|cadmium-translocating-P-type-ATPase	unknown	unknown	gnl|CDD|319849
NZ_LN831776.1|WP_167345678.1|6944354_6944516_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426829.1|6944039_6944234_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426826.1|6939338_6940835_-|xylulokinase	unknown	unknown	gnl|CDD|198374
NZ_LN831776.1|WP_020426823.1|6934433_6935414_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_046505782.1|6933462_6934371_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	3.14941e-60
NZ_LN831776.1|WP_020426839.1|6958308_6959109_+|polysaccharide-deacetylase-family-protein	gnl|CDD|200589	cd10967, CE4_GLA_like_6s, Putative catalytic NodB homology domain of gellan lyase and similar proteins. This family is represented by the extracellular polysaccharide-degrading enzyme, gellan lyase (gellanase, EC 4.2.2.-), from Bacillus sp. The enzyme acts on gellan exolytically and releases a tetrasaccharide of glucuronyl-glucosyl-rhamnosyl-glucose with unsaturated glucuronic acid at the nonreducing terminus. The family also includes many uncharacterized prokaryotic polysaccharide deacetylases, which show high sequence similarity to Bacillus sp. gellan lyase. Although their biological functions remain unknown, all members of the family contain a conserved domain with a 6-stranded beta/alpha barrel, which is similar to the catalytic NodB homology domain of rhizobial NodB-like proteins, belonging to the larger carbohydrate esterase 4 (CE4) superfamily.	4.90158e-56
NZ_LN831776.1|WP_020426825.1|6937393_6939178_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	4.12402e-63
NZ_LN831776.1|WP_020426832.1|6946054_6946996_-|thioredoxin-disulfide-reductase	gnl|CDD|273540	TIGR01292, Thioredoxin_reductase, thioredoxin-disulfide reductase. This model describes thioredoxin-disulfide reductase, a member of the pyridine nucleotide-disulphide oxidoreductases (pfam00070). [Energy metabolism, Electron transport].	4.35858e-159
NZ_LN831776.1|WP_020426824.1|6935843_6937397_-|response-regulator-transcription-factor	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	4.1481e-55
NZ_LN831776.1|WP_020426834.1|6949554_6952029_-|hypothetical-protein	gnl|CDD|225990	COG3459, COG3459, Cellobiose phosphorylase [Carbohydrate transport and metabolism].	0
NZ_LN831776.1|WP_020426828.1|6942748_6943909_+|ROK-family-transcriptional-regulator	gnl|CDD|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	3.99567e-66
NZ_LN831776.1|WP_020426837.1|6956860_6957727_+|AraC-family-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	5.21181e-28
NZ_LN831776.1|WP_020426831.1|6945665_6945899_-|glutaredoxin-family-protein	gnl|CDD|239274	cd02976, NrdH, NrdH-redoxin (NrdH) family; NrdH is a small monomeric protein with a conserved redox active CXXC motif within a TRX fold, characterized by a glutaredoxin (GRX)-like sequence and TRX-like activity profile. In vitro, it displays protein disulfide reductase activity that is dependent on TRX reductase, not glutathione (GSH). It is part of the NrdHIEF operon, where NrdEF codes for class Ib ribonucleotide reductase (RNR-Ib), an efficient enzyme at low oxygen levels. Under these conditions when GSH is mostly conjugated to spermidine, NrdH can still function and act as a hydrogen donor for RNR-Ib. It has been suggested that the NrdHEF system may be the oldest RNR reducing system, capable of functioning in a microaerophilic environment, where GSH was not yet available. NrdH from Corynebacterium ammoniagenes can form domain-swapped dimers, although it is unknown if this happens in vivo. Domain-swapped dimerization, which results in the blocking of the TRX reductase binding site, could be a mechanism for regulating the oxidation state of the protein.	1.00436e-22
NZ_LN831776.1|WP_020426827.1|6941024_6942344_-|xylose-isomerase	gnl|CDD|235487	PRK05474, PRK05474, xylose isomerase; Provisional.	0
NZ_LN831776.1|WP_020426830.1|6945084_6945525_-|GNAT-family-N-acetyltransferase	gnl|CDD|379228	pfam13508, Acetyltransf_7, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.19109e-07
NZ_LN831776.1|WP_039786316.1|6931576_6933295_-|extracellular-solute-binding-protein	gnl|CDD|270300	cd13582, PBP2_AlgQ_like_3, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	0
NZ_LN831776.1|WP_020426833.1|6947199_6949155_-|cadmium-translocating-P-type-ATPase	gnl|CDD|319849	cd07551, P-type_ATPase_HM_ZosA_PfeT-like, P-type heavy metal-transporting ATPase, similar to Bacillus subtilis ZosA/PfeT which transports copper, and perhaps zinc under oxidative stress, and perhaps ferrous iron. Bacillus subtilis ZosA/PfeT (previously known as YkvW) transports copper, it may also transport zinc under oxidative stress and may also be involved in ferrous iron efflux. ZosA/PfeT is expressed under the regulation of the peroxide-sensing repressor PerR. It is involved in competence development. Disruption of the zosA/pfeT gene results in low transformability. This subfamily belongs to the P-type ATPases, a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids, and are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle.	0
NZ_LN831776.1|WP_020426826.1|6939338_6940835_-|xylulokinase	gnl|CDD|198374	cd07808, FGGY_D-XK_EcXK-like, Escherichia coli xylulokinase-like D-xylulose kinases; a subgroup of the FGGY family of carbohydrate kinases. This subgroup is predominantly composed of bacterial D-xylulose kinases (XK, also known as xylulokinase; EC 2.7.1.17), which catalyze the rate-limiting step in the ATP-dependent phosphorylation of D-xylulose to produce D-xylulose 5-phosphate (X5P) and ADP. D-xylulose has been used as a source of carbon and energy by a variety of microorganisms. Some uncharacterized sequences are also included in this subgroup. The prototypical member of this CD is Escherichia coli xylulokinase (EcXK), which exists as a dimer. Each monomer consists of two large domains separated by an open cleft that forms an active site. This model includes both the N-terminal domain, which adopts a ribonuclease H-like fold, and the structurally related C-terminal domain. The presence of Mg2+ or Mn2+ is required for catalytic activity. Members of this subgroup belong to the FGGY family of carbohydrate kinases.	0
NZ_LN831776.1|WP_046505789.1|6952060_6956092_-|glycoside-hydrolase-family-2	gnl|CDD|225789	COG3250, LacZ, Beta-galactosidase/beta-glucuronidase [Carbohydrate transport and metabolism].	1.46519e-48
NZ_LN831776.1|WP_020426823.1|6934433_6935414_-|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	1.36738e-133

Protein sequences

>NZ_LN831776.1|WP_167345678.1|6944354_6944516_-|hypothetical-protein
MLRNNGRNAVVEAQTVGVLRNNGGNAVVEAQTVDVFRNNGKNAVVEALEVSLL
>NZ_LN831776.1|WP_020426829.1|6944039_6944234_+|hypothetical-protein
MTYVDTSDISAQMFITVLLLLLIIAPLISLGVLRLFQSRKKSGLLLIVSGIAVYALFQIIMYFI
>NZ_LN831776.1|WP_020426828.1|6942748_6943909_+|ROK-family-transcriptional-regulator
MKVTGDQALVKKINKSIILHTIRKHSPVSRARVSEMTGLNKATVSNLVSELCGQELVTEAGPGESSGGRKPLMLHFNSMAGSVIGIELQVKQLKAVLCDLGGSTLQELDCPLEVHDLPYVLEKMKAIISELIASAPSSPYGIVGIGVGVPGMVDEHGMVLFAPNLGWEMVDLRAILEQSFAVPVTIDNEANAGAQGELNFGAARDVRHLLYISAGSGIGSGIIIGGELYKGARGYAGETGHMTIEAEGKPCSCGSRGCWELYASERTYDNPGLALPARSTTELVRYAHEGQEDTLRHFTTIGEYLGIGVTNLINSFNPELIVIGGALSEAEPWLGEPLRRVVAERTLPYHKQQLEITFSRLGSRGTMIGAGFSAVMHFLGNIRVTL
>NZ_LN831776.1|WP_020426827.1|6941024_6942344_-|xylose-isomerase
MAYFESVGKISYEGSRSTNPYAFKFYNPKEIVAGKTMEEHLKFAMAYWHTLTAGGSDPFGAETAVRAWDKLSTLDKAKARAEAAFEFMEKMDLHYYCFHDVDIAPEGASLREFYSNIDTIVDILEQGMKASGKKLLWNTANMFTNPRYMHGAGSTCNADVYAHAAAQVKKGLEVGKRLGADNYVFWGGREGYETLLNTDMSLEQDNIARLFSMAVDYAKEIGFDGQFLIEPKPKEPTKHQYDFDAATTIAFLQKYNLDKHFKLNLEANHATLAGHTFEHELRVARINGMLGSLDANQGDPLLGWDTDEFPASIYDATLTLYEVLKNDGLGKGGINFDSKVRRPSFEPEDLFLAHISGMDIYAKGLKVAAKLLEDRVFENFIDKRYSSFTEGVGADIVSGKATLASLADYALNNENPRKNESGRQELLRATLNQYILAEQ
>NZ_LN831776.1|WP_020426826.1|6939338_6940835_-|xylulokinase
MKYVIGVDLGTSAVKTVLVDPQGKVAFEHSESYPLSRPQPNWSEQNPEDWVQGTLVSLRRLIEVSGVDPSQVDGISFSGQMHGLVLVDREGKVLRPAILWNDTRTTAQCRKIEQTLGSKLIGIARNRALEGFTLPKILWVQENEPEVLAQAALFLLPKDYVRYRLTGDYAMDYSDAAGTLLLDVGAKTWSAEIAEAFGLPFSLCPKLVESFDLTGTLLPEIAEASGLLPSTKVFAGGADNACGALGAGILGEGRTMCSIGTSGVVLSYESNKDLNLEGKVHFFNHGEKDAYYIMGVTLAAGYSLTWFKETFAGDKSFDELLQGVDSIPAGSGGLLFTPYIVGERTPHPDPNIRGSFIGMDAGHTLAHFTRSVLEGITFSLRESIDIVRDSGKEITEVVAIGGGAKNEAWLQMQADIFNASIIKLESEQGPAMGAAMLAAYGSGWFASLSECAEAFIRPAEVYKPNAQQAEVYNGLFHLYQQVYGQTRELNDKLAAYRK
>NZ_LN831776.1|WP_020426825.1|6937393_6939178_-|sensor-histidine-kinase
MFHWFVKLMNDIKIRNKLLLAFLGVTLLPVLLVGGYLTFEMRTMAFDNALEQASTNVDRVRKRTEEVIGVSQDISYRLNNDTRLKRLAVRKYESIYEVVKAYQDYTDVREYIRLYSEISNIRLYTDNSSLLNNWELINPSPAIKESEWYQRAQRYEGLVGWEYIEDERDHHKYLSLVRKIELEGSSKTGVLVINVNSNKLTSILNQESFDTMIVDDQNNIIASNRKEREGKTLADISFDTKLLGRGSGSYEAVVEGEPSQIVIDELSPQASRNALRVVSVFSIDSIVKEPNRIIRLALSVIAISVVLAFLLIFSFSSLFSRRLLHLSKHINRVGTGDFDTSLQIDGKDEIALLARQFNSMVRSIHDLMLEVQVSNEQNSLLQQKQNDIRFKMLASQINPHFLFNALESIRMEAHMKNQQEIARVVRLLGQMMRSSLEVGRSKVTLKQELDMVRCYLEIQQFRYEERLKYHFIVDPAIESLSMPPLIIQPLVENAVIHGLDNTLEGAVVTVEIRYEQEHAVFTITDNGVGITQDRLEQVRSTLETQEEQEGARIGLRNVHDRLKLSYGEKYGLTIESHPDEGTRISFRIPMEVAK
>NZ_LN831776.1|WP_020426824.1|6935843_6937397_-|response-regulator-transcription-factor
MMIKVLIVDDEPKLREGLRALIPWGQLGFTVVATAANGLQALEKYHIHDPELIVVDIRMPGMDGLELIGELRNEGSTSHVLILSGHADFDYAKRAIGYRIDGYLLKPVDEEEMISLLKELRETIDREDRFSRWNEEEPTRNRESLLRALLQPPAEESGADDPGKQAAALGLTPGRVEVVLIELLAPAHAIEEEERKIIAAVEQHFSGSGDRLFFTLPPYIGLLLKEPLQDGMRRERLIEELAGLICPCGFNFTAAAGGAVPRPEEAAESFNAARDLLRRAFFYRKGMMLTADPSGMLFPDSGEADTEQVTDAESRLLLAVETGSRAAIEPLVQAISAGLIAAGGEEQQIKDTFVRILSTVLARLEPVYPEIRNNTVKHFPPIGELYQSHYLEDLQEQSVAFLAEIAGQMTSGVKGNEIKKITELIQRRYNENLKLETLSELFSYNSAYLGKMFKNTTGEYFNTYLDKVRIEKAKEFLAQGMKVYEVAEKVGYMNSDYFNAKFRKYVGTSPSSFRKNK
>NZ_LN831776.1|WP_020426823.1|6934433_6935414_-|sugar-ABC-transporter-permease
MKADTATAPIPPDTRKRNKKPASGGRFWRNFKNQKYLWMMSIPFVIWAFVFSYLPLWGWTMAFQKYKPARGFFEQEWVGFDHFKTLFSDSQFLLALRNTLAMSGMGLVAGFIFPITFAILLNEVRLGIFKRFAQTVSYLPHFVSWVVAAGIVTKMLSSENGLVNDILLGIGFIDSPIQFMAQGHLFWGIVTLSDVWKETGWNAIIYLAAISGIGPELYEASRVDGASRLRQVWHITLPGIRPTIIVLLIMSIGNLLNIGFEKQFLLQNNLVTDYSQVLDLYSLKYGLGMARYSYGTAINIFNSVISVILLFTINGIFKRTTKESLL
>NZ_LN831776.1|WP_046505782.1|6933462_6934371_-|carbohydrate-ABC-transporter-permease
MVGNTALTGKSWADRIFDFIVYLVVLIVIVVTIYPFLNVLAISLNDSVDSVRGGITIYPREFTWDNYLKIFTFSGLVTGFKISALRTVAGTLLGLISASMLAFTVSRPDFQGRKFVSTFLAMTMYISGGMIPVYMLVKDLGMMNSFAVYIVPGLVSAFNVFVIRSFIDGLPYALQESAKLDGANDFTIYLRVILPLLKPALATISLFLAVGQWNAWFDTYLYNGSSPHLTTLQYELMKVLQTTTSGNNGDYRSNIASMASNQVSPESLKMAITIVVTVPILMVYPFIQKYFVKGMTLGAVKS
>NZ_LN831776.1|WP_039786316.1|6931576_6933295_-|extracellular-solute-binding-protein
MKAKASAITLTSVMLLGLLAGCGGNNGNNAAGNAANTGNNANKAEDTSPLTMTYFSADPNPNWTGMQDEVGKVLTEKTGVTLEAEFAVGDPQQKVALIAASGEYPDLISAKTDISKLVDAGAMLDLTDLIDKYAPNIKKVLGEEGLKRSRYSDDDHAIYAIPTYAGVDNKYFDAGGGFELQHRAVKEAGYPEIKTVQDYENVIKAYLEKHPTDENGNKNIGMTLNADDWYMYITVTNPAFITTGSPDDGEYAIDIDTQEVTYHFRRPAEKEYFRWLNHMNDIGLLDPESFVQKYDQYKAKIATGRVIGLIDQDWGYGDGEKALKAAGKLDQGYAHFPVTLSEEYKDTSFWPTGFMAGNGVGISVDAKDPVRAIKFLDYLASDEGQVLINWGIEGKHYNVVDGKRVIPEDVNNRKYNDTTNFQKETGLGNVGSSYALLSAHYGDGVLDPTGSYYTTRFPEQVTAGYNKVEKETLAAYKANTWKDLFPSEDEFKVKPWGAAWNITIPGDSEIVVLDNKLKDITWKRIPEAILSKPADFDKVWDAYMGELDKAGVSKAEDLREELVKKRVKLWNE
>NZ_LN831776.1|WP_020426830.1|6945084_6945525_-|GNAT-family-N-acetyltransferase
MLISLKNYWDRDAVERLLAECMEAGAAEIAEEVDRYLTGDSRELLGTFVNGELAGLAGIRHEPGEAIGLLHIAVQARLRGRGIGRAMIEELRRCQGNDMLRAETDLAGAGFFRKSGFVVTSLSEKDPGVERFDCVLPVSSQAEYAL
>NZ_LN831776.1|WP_020426831.1|6945665_6945899_-|glutaredoxin-family-protein
MENVIVYTSTNCPHCRQVKSFLSEKGISYEERNIEQNDDYAQQVWDMGMRAVPVTVIGDFKIVGMNKTQFDKALANV
>NZ_LN831776.1|WP_020426832.1|6946054_6946996_-|thioredoxin-disulfide-reductase
MYKSIIIGTGPAGLTAAIYLARANLNPLVIEGPQPGGQLTTTTEVENFPGFPDGIMGPELMDNMRKQAERFGAKFVTGWVNSVELGERPFKLNVEGMGALTTDTLILSTGATAKYLGIPGEQDNIGRGVSTCATCDGFFFRGKEIVVVGGGDSALEEAGFLTRFASKVTLVHRREELRASKIMQDRVRDNEKVAWSLNRTPLEVTSGDRGVNGIKVLNNVTGEEEFIEASGVFVAIGHHPNTAFLGGQITTDANGYIVTNPGTSETNIPGVFACGDVQDTRYKQAITAAGSGCMAAMDAEKYIESLEHSAVIL
>NZ_LN831776.1|WP_020426833.1|6947199_6949155_-|cadmium-translocating-P-type-ATPase
MQATSKQLPKSLAREGSAQQPRTPRPRRFDPKAMLSNAEMQAALGSGLLLLIAWAVSGWSEIFSILLYIVSYSVGGWIKAKEGVETLVKERDLDVNLLMIAAALGAASIGYWNEGAMLIFIFALSGALESYTMERSKKDISSLMALKPATAVRIEKGGMSEVAIDLLAVGDQLLVRPGEIIPADGTVYRGESAVNQASITGESLPVEKSAGSDVFAGTINGEGPLYIEVTKSAENTLFAKIIKMVEEAETEVPESQRFIKRLESIYARVVVAATAALIALPPFLLDWSWSAAFYKAMVFLVVASPCALVSSIMPAMLSAISKSARKGILFKGGVHLENMAKTSVVAFDKTGTLTEGLPQVTDFIAGEGYDRTELLAVSASIEKLSRHPLAEAIVRKAEEEHLVLHVIEESTSVTGWGIEGLIEGRLWRIGKSNLLDERNEDGDEQWKTLRRQLEKEGKTVSLILDVEKIAGMIALQDTVRPQAVAAVRKLQELGVKVAMLTGDRAATAEVIAGQTGVDLVFAGLLPEDKVTHIKALRKQYGNVVMVGDGVNDAPALATATVGIGMGMKGSGAALEIADVVLMNDNIEEIASTITLARRSQRIVKQNMVFAVTVIATLMLSNFLQGIALPFGVVGHEGSTILVILNGLRLLR
>NZ_LN831776.1|WP_020426834.1|6949554_6952029_-|hypothetical-protein
MMKQPGPASPAGLSGSKEHKKGVVKTAGGAAVVREQQLDQYFTFRDELKEVEFKRHDMPTPWMNYLSNGTFHTMLSHAGGGVAFYKSPQIWRITRYRFFHLPTDRSGPYIYLQDAGTGRYWCPTYEPAFQKPQEWSSSHGLGYTRFEAQEDEVAAKTVYFVGPYENSLIWNLTLTNNSPAVKVLNVYAYAEFGMMEFMRELQWQCYNKHQVSVQYHPKEALVYKYGVENQPKPEETPLVYMMSDTPLHSYDGDREEFIGSYRSESNPAAIEQGGCTGSTLLGGDPCGALQVQVTLQPGETRTVNFFLGTAMDEVEVEQAIEHSREADFVARSYAALKENWDSYLGAWNCELPDADAQRMLNIWNPYQAQRNFLFSRNISFYATGTFRGVGFRDTAQDILAVAPFDPEAAKEKVRLLLGQQYQDGHVNHYFFPNEGWDPVTSIHSDDHLWTALAVWDILAETGDAGFLQESLPFYDGGEGTLYEHLKRAIDFTASRLGPNGFPLMLRSDWNDQLFRVCRQGKGESIWTAMQLGTVLLRMKDLAAASGHPEHAAGYEAMYENQKDLVNTLGWDGQWFRRAVMDDGRFLGTDEHDEAKIWLNAQTWATLSGMAEPDKAVQAMDSVRDILDTELGIKKLHPSITTFPDPADPLTNYNKGTGENGAVFCHANTWAIIAECMLGRGDQAYKYYRQLIPNVAMEQAGIWRYKAEPYVYASNLFGPESDKFGLANVSWLTGTAAWMYIAATQYIMGIKPVLEGLSIDPCIPSEWEGFTVNRRFRGCLYEISVTNSSHNCKGVKEIRVDGQRLEGNIVPAYPEKAMVKVEVIL
>NZ_LN831776.1|WP_046505789.1|6952060_6956092_-|glycoside-hydrolase-family-2
MRTSICLNGEWDFMPLYGQPLNRTLPERLVYEARKVQVPSSWRHGYPQPSGKKFGEVAEHGFAPLDVYGYPREWDAAEAGVLHRSFQVPETMLGQRIVLRFDGIMQKAAVYLDRERIAVWEDGYLPLRLDISSRVKPGEEQHLHVVCGSFDQTVLPSGDRKITGLAGSWFGRMARGIWQDVFLESYPLVTLEDITIRTLFRQGLLEVDALIGTESGSAYAEPLRVFLKVNDRKPGALPVLEAEAGAEAVPLQAGEGRQLCENADNREWQKARFVLSWPDARLWSPETPNLYELELELRAGGETLDRRTGTFGFREFWCEGPQFMLNGTPVNLRGDSWHFQGAAQQTEGYIRNWYRMCRQAGVNSIRLHAEPYPSDYLRIADEEGMLIVDETAIYGSSKSMDANHPDFIANCRAHVQRLVQRDKNHPSVILWSVQNEMRWVDGRDGYKQHIPGLMKLMRDLDSTRPIMVEGDNRLLPKELTEVESRHYNIDGTISQWDRTVPLTFGEHGGWWYICPQNSSMYVGLGAYRDTDASAAGLAQKERLFVEYARRQGVSGISTFNFVHYFMRAMPDRDIALPPADLTEPGPKPVLIPAYSLSLNNGLLPEEYPAYRVNPSFDIMAEAFKPVTMIAAEYNRCFFDDSPIRRSFDVYNDTLAEQAVTIECTVQQDGRVVHTRAFSFRQEPAERRCIRLEWMPDSVDGEGEAVLAARLFHGGELKHELSLSYRLLSGSCKTAPVALELPAVYTGSDRDYEVIKVLVPDLDRIDPEAIEQLPGGILLIVGSKMPDMDGGLDRKLRGFVQQGGRLLLLEQLHLSPGKLPLVRREFIRAQAGSYEHPVLQGLGDEDLMFWHEELREEGPLPIIKAAFEKPVTGDFTLLLECSSGDFGDGGDLWSPLLEYRNGAGMFLANQLEIMDHLHRIPQACLLLRGLLRYAGRAVPAAAAPVPAAVWVRSGSPAEALLRKLRLKGTWLDSAAGLSSLSPGLLVVEAGLLNGPGAAEAVRQAASAGSRVLVLPAEPGGQEALARLLDRPVRIAPHGTYHLEADYAHAAVQGFSPVDLFGFDKVFLSPRDVVNRELALHRLEVPDAEVLCTSVEGTAWKDYFAGQHTAEYSRLALVELNRDKAREPGGFLIRIAAGEGEIICSQLLTEADSDKSLRLYTRLLGNMGAAFADELLIRDKGDAEWAVETAMVLPCPPYVDYQAMKDYYTDPEFSLNNLGEGLYGWMKKKERRADGTLLIPDPAGCPVFLSCFVHLPALSEDSRTGNVRTGRLQVQSDNAFEIYMNGEQVAAPEKEIRLSSGINRLIAIVQGGREDFAFGMVFLNSDGTYMNDLEYRLTMDEVEPK
>NZ_LN831776.1|WP_020426836.1|6956097_6956763_-|hypothetical-protein
MQRCLYRGECREGGVPESFFPSRLQQLNERMELLDVTRLSIFKGGKELFLYYECGGERHEPEKLLADNGELLQVWPGGEQPRWWAPMMDIFHYQQPVSREYWKRSQGERTPFGRVAVLKPEQVSSYVYYHYQYQEERPGDGDKYGIIGLHENLLFFYSELPATVEPVPYSGKLTTNLRPEHWGEVMEPHFIKWGDAQPDQEIWKKLTMVLNVAVPAGKKEE
>NZ_LN831776.1|WP_020426837.1|6956860_6957727_+|AraC-family-transcriptional-regulator
MTNKLYARDLGLEPGFTFRIQKCPLTHDYYVHSHDFSELVVILEGSAIHIIEGREYPVSAGQVFFIHSDISHGYKNVQNIQYVNVMFHPDQLLQLPELKLLPGFQALFYLEPFFRKEMFFKGMLSLEPRQLDEVNLLLDRILEEHDRQSDGYRLMIRTYFTALVGTLSRYYRQNGGGTENKALRIGEAITYIEEHFLQPVSLQDLADLAFMSKRQFLRVFTRNYHTTPMDYIIRKRLDYSCTLLRNPELSISQVAMDSGFRDHNYYSRQFKKVFLCTPSEYRTHKAGL
>NZ_LN831776.1|WP_046505792.1|6957926_6958127_+|hypothetical-protein
MAQAIGESGLTIAGFPGTAPATSLQGRINGIFAVVSRLADVLRLNNGTFAVVFTDHGCAAPNNGTF
>NZ_LN831776.1|WP_020426839.1|6958308_6959109_+|polysaccharide-deacetylase-family-protein
MKIKLDLFPGGVTKALTTSWDDGRIYDRQLVAVLNRHGLKGSFHLNSGFFGKDSYITREEAASLYKGHEISAHTCTHPFLSMTPREGIAEEVLRDREHLEQIAGYPVRGMSYPFGDYNDGVLSILPALGIEYSRTVQSHGSFILPDNPLAWHPTCHHRDMLALGQQFLEEKPKYPRMQLLYVWGHSYEFNDNNNWEELEQFAGMMGGHEDIWYATNIEIVDYLSAVRGLRFSASRSIVYNPSAVDVWITAEDQVRQIPSGATLQLD

Crispr_ID: NZ_LN831776_70

• CRISPR_ID: NZ_LN831776_70
• CRISPR_location: 6958010-6958134
• CRISPR_type: TypeV
• Repeat_type: NA
• Spacer_info: 2 spacers
• Cas_protein_info: cas14j

Consensus repeat of NZ_LN831776_70

Consensus_repeat	Method
CAACGGCATTTTTGCCGTTGTTT	CRISPRCasFinder

spacers of NZ_LN831776_70

>70.1|6958033|28|NZ_LN831776|CRISPRCasFinder
CACGGCTAGCTGACGTGCTGAGGCTTAA
>70.2|6958084|28|NZ_LN831776|CRISPRCasFinder
TCACCGATCACGGCTGCGCCGCGCCTAA

CRISPR arrays and Neighbor proteins around NZ_LN831776_70

CRISPR arrays

The CRISPR arrays of NZ_LN831776_70

>merge|NZ_LN831776|70|6958010-6958134|CRISPRCasFinder
CAACGGCATTTTTGCCGTTGTTTCACGGCTAGCTGACGTGCTGAGGCTTAACAACGGCACTTTTGCCGTTGTTTTCACCGATCACGGCTGCGCCGCGCCTAACAACGGCACTTTTTAAAATGTTA

>NZ_LN831776|70|70|6958010-6958134|CRISPRCasFinder
CAACGGCATTTTTGCCGTTGTTT	CACGGCTAGCTGACGTGCTGAGGCTTAA
CAACGGCACTTTTGCCGTTGTTT	TCACCGATCACGGCTGCGCCGCGCCTAA
CAACGGCACTTTTTAAAATGTTA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020425892.1|6966181_6967522_-|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_LN831776.1|WP_020425891.1|6965243_6966110_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_046504599.1|6959589_6960669_-|IS200/IS605-family-element-transposase-accessory-protein-TnpB	cas14j	-	gnl|CDD|223747
NZ_LN831776.1|WP_020426832.1|6946054_6946996_-|thioredoxin-disulfide-reductase	unknown	unknown	gnl|CDD|273540
NZ_LN831776.1|WP_039785258.1|6961295_6963296_-|alpha-L-arabinofuranosidase	unknown	unknown	gnl|CDD|377497
NZ_LN831776.1|WP_020426836.1|6956097_6956763_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_046505798.1|6967672_6968536_-|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_020426839.1|6958308_6959109_+|polysaccharide-deacetylase-family-protein	unknown	unknown	gnl|CDD|200589
NZ_LN831776.1|WP_046505789.1|6952060_6956092_-|glycoside-hydrolase-family-2	unknown	unknown	gnl|CDD|225789
NZ_LN831776.1|WP_020426831.1|6945665_6945899_-|glutaredoxin-family-protein	unknown	unknown	gnl|CDD|239274
NZ_LN831776.1|WP_020426834.1|6949554_6952029_-|hypothetical-protein	unknown	unknown	gnl|CDD|225990
NZ_LN831776.1|WP_020426830.1|6945084_6945525_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379228
NZ_LN831776.1|WP_167345565.1|6961066_6961225_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425895.1|6968806_6968995_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426833.1|6947199_6949155_-|cadmium-translocating-P-type-ATPase	unknown	unknown	gnl|CDD|319849
NZ_LN831776.1|WP_081487080.1|6964355_6965120_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_167345678.1|6944354_6944516_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425889.1|6963341_6964295_-|family-43-glycosylhydrolase	unknown	unknown	gnl|CDD|350141
NZ_LN831776.1|WP_020426829.1|6944039_6944234_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426837.1|6956860_6957727_+|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225117

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831776.1|WP_046504599.1|6959589_6960669_-|IS200/IS605-family-element-transposase-accessory-protein-TnpB	cas14j	-	9.5e-104	342.6	14.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020425892.1|6966181_6967522_-|sugar-ABC-transporter-substrate-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.3192e-85
NZ_LN831776.1|WP_020425891.1|6965243_6966110_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.81708e-90
NZ_LN831776.1|WP_046504599.1|6959589_6960669_-|IS200/IS605-family-element-transposase-accessory-protein-TnpB	gnl|CDD|223747	COG0675, COG0675, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	1.32834e-55
NZ_LN831776.1|WP_020426832.1|6946054_6946996_-|thioredoxin-disulfide-reductase	gnl|CDD|273540	TIGR01292, Thioredoxin_reductase, thioredoxin-disulfide reductase. This model describes thioredoxin-disulfide reductase, a member of the pyridine nucleotide-disulphide oxidoreductases (pfam00070). [Energy metabolism, Electron transport].	4.35858e-159
NZ_LN831776.1|WP_039785258.1|6961295_6963296_-|alpha-L-arabinofuranosidase	gnl|CDD|377497	pfam05270, AbfB, Alpha-L-arabinofuranosidase B (ABFB) domain. This family consists of several fungal alpha-L-arabinofuranosidase B proteins. L-Arabinose is a constituent of plant-cell-wall poly-saccharides. It is found in a polymeric form in L-arabinan, in which the backbone is formed by 1,5-a- linked l-arabinose residues that can be branched via 1,2-a- and 1,3-a-linked l-arabinofuranose side chains. AbfB hydrolyzes 1,5-a, 1,3-a and 1,2-a linkages in both oligosaccharides and polysaccharides, which contain terminal non-reducing l-arabinofuranoses in side chains.	2.60234e-42
NZ_LN831776.1|WP_046505798.1|6967672_6968536_-|AraC-family-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.21098e-24
NZ_LN831776.1|WP_020426839.1|6958308_6959109_+|polysaccharide-deacetylase-family-protein	gnl|CDD|200589	cd10967, CE4_GLA_like_6s, Putative catalytic NodB homology domain of gellan lyase and similar proteins. This family is represented by the extracellular polysaccharide-degrading enzyme, gellan lyase (gellanase, EC 4.2.2.-), from Bacillus sp. The enzyme acts on gellan exolytically and releases a tetrasaccharide of glucuronyl-glucosyl-rhamnosyl-glucose with unsaturated glucuronic acid at the nonreducing terminus. The family also includes many uncharacterized prokaryotic polysaccharide deacetylases, which show high sequence similarity to Bacillus sp. gellan lyase. Although their biological functions remain unknown, all members of the family contain a conserved domain with a 6-stranded beta/alpha barrel, which is similar to the catalytic NodB homology domain of rhizobial NodB-like proteins, belonging to the larger carbohydrate esterase 4 (CE4) superfamily.	4.90158e-56
NZ_LN831776.1|WP_020425889.1|6963341_6964295_-|family-43-glycosylhydrolase	gnl|CDD|350141	cd18820, GH43_LbAraf43-like, Glycosyl hydrolase family 43 proteins similar to Lactobacillus brevis alpha-L-arabinofuranosidase LbAraf43 and Geobacillus thermoleovorans GbtXyl43B. This uncharacterized glycosyl hydrolase family 43 (GH43) subgroup belongs to a subgroup which includes enzymes with beta-xylosidase (EC 3.2.1.37), alpha-L-arabinofuranosidase (EC 3.2.1.55) and possibly bifunctional xylosidase/arabinofuranosidase activities, similar to Lactobacillus brevis alpha-L-arabinofuranosidase LbAraf43 and Geobacillus thermoleovorans IT-08 beta-xylosidase / exo-xylanase (GbtXyl43B). It belongs to the glycosyl hydrolase clan F (according to carbohydrate-active enzymes database (CAZY)) which includes family 43 (GH43) and 62 (GH62) families. GH43 are inverting enzymes (i.e. they invert the stereochemistry of the anomeric carbon atom of the substrate) that have an aspartate as the catalytic general base, a glutamate as the catalytic general acid and another aspartate that is responsible for pKa modulation and orienting the catalytic acid. Many GH43 enzymes display both alpha-L-arabinofuranosidase and beta-D-xylosidase activity using aryl-glycosides as substrates. A common structural feature of GH43 enzymes is a 5-bladed beta-propeller domain that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	5.55925e-129
NZ_LN831776.1|WP_020426831.1|6945665_6945899_-|glutaredoxin-family-protein	gnl|CDD|239274	cd02976, NrdH, NrdH-redoxin (NrdH) family; NrdH is a small monomeric protein with a conserved redox active CXXC motif within a TRX fold, characterized by a glutaredoxin (GRX)-like sequence and TRX-like activity profile. In vitro, it displays protein disulfide reductase activity that is dependent on TRX reductase, not glutathione (GSH). It is part of the NrdHIEF operon, where NrdEF codes for class Ib ribonucleotide reductase (RNR-Ib), an efficient enzyme at low oxygen levels. Under these conditions when GSH is mostly conjugated to spermidine, NrdH can still function and act as a hydrogen donor for RNR-Ib. It has been suggested that the NrdHEF system may be the oldest RNR reducing system, capable of functioning in a microaerophilic environment, where GSH was not yet available. NrdH from Corynebacterium ammoniagenes can form domain-swapped dimers, although it is unknown if this happens in vivo. Domain-swapped dimerization, which results in the blocking of the TRX reductase binding site, could be a mechanism for regulating the oxidation state of the protein.	1.00436e-22
NZ_LN831776.1|WP_020426834.1|6949554_6952029_-|hypothetical-protein	gnl|CDD|225990	COG3459, COG3459, Cellobiose phosphorylase [Carbohydrate transport and metabolism].	0
NZ_LN831776.1|WP_020426830.1|6945084_6945525_-|GNAT-family-N-acetyltransferase	gnl|CDD|379228	pfam13508, Acetyltransf_7, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.19109e-07
NZ_LN831776.1|WP_046505789.1|6952060_6956092_-|glycoside-hydrolase-family-2	gnl|CDD|225789	COG3250, LacZ, Beta-galactosidase/beta-glucuronidase [Carbohydrate transport and metabolism].	1.46519e-48
NZ_LN831776.1|WP_020426833.1|6947199_6949155_-|cadmium-translocating-P-type-ATPase	gnl|CDD|319849	cd07551, P-type_ATPase_HM_ZosA_PfeT-like, P-type heavy metal-transporting ATPase, similar to Bacillus subtilis ZosA/PfeT which transports copper, and perhaps zinc under oxidative stress, and perhaps ferrous iron. Bacillus subtilis ZosA/PfeT (previously known as YkvW) transports copper, it may also transport zinc under oxidative stress and may also be involved in ferrous iron efflux. ZosA/PfeT is expressed under the regulation of the peroxide-sensing repressor PerR. It is involved in competence development. Disruption of the zosA/pfeT gene results in low transformability. This subfamily belongs to the P-type ATPases, a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids, and are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle.	0
NZ_LN831776.1|WP_081487080.1|6964355_6965120_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.2922e-79
NZ_LN831776.1|WP_020426837.1|6956860_6957727_+|AraC-family-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	5.21181e-28

Protein sequences

>NZ_LN831776.1|WP_020426837.1|6956860_6957727_+|AraC-family-transcriptional-regulator
MTNKLYARDLGLEPGFTFRIQKCPLTHDYYVHSHDFSELVVILEGSAIHIIEGREYPVSAGQVFFIHSDISHGYKNVQNIQYVNVMFHPDQLLQLPELKLLPGFQALFYLEPFFRKEMFFKGMLSLEPRQLDEVNLLLDRILEEHDRQSDGYRLMIRTYFTALVGTLSRYYRQNGGGTENKALRIGEAITYIEEHFLQPVSLQDLADLAFMSKRQFLRVFTRNYHTTPMDYIIRKRLDYSCTLLRNPELSISQVAMDSGFRDHNYYSRQFKKVFLCTPSEYRTHKAGL
>NZ_LN831776.1|WP_020426836.1|6956097_6956763_-|hypothetical-protein
MQRCLYRGECREGGVPESFFPSRLQQLNERMELLDVTRLSIFKGGKELFLYYECGGERHEPEKLLADNGELLQVWPGGEQPRWWAPMMDIFHYQQPVSREYWKRSQGERTPFGRVAVLKPEQVSSYVYYHYQYQEERPGDGDKYGIIGLHENLLFFYSELPATVEPVPYSGKLTTNLRPEHWGEVMEPHFIKWGDAQPDQEIWKKLTMVLNVAVPAGKKEE
>NZ_LN831776.1|WP_046505789.1|6952060_6956092_-|glycoside-hydrolase-family-2
MRTSICLNGEWDFMPLYGQPLNRTLPERLVYEARKVQVPSSWRHGYPQPSGKKFGEVAEHGFAPLDVYGYPREWDAAEAGVLHRSFQVPETMLGQRIVLRFDGIMQKAAVYLDRERIAVWEDGYLPLRLDISSRVKPGEEQHLHVVCGSFDQTVLPSGDRKITGLAGSWFGRMARGIWQDVFLESYPLVTLEDITIRTLFRQGLLEVDALIGTESGSAYAEPLRVFLKVNDRKPGALPVLEAEAGAEAVPLQAGEGRQLCENADNREWQKARFVLSWPDARLWSPETPNLYELELELRAGGETLDRRTGTFGFREFWCEGPQFMLNGTPVNLRGDSWHFQGAAQQTEGYIRNWYRMCRQAGVNSIRLHAEPYPSDYLRIADEEGMLIVDETAIYGSSKSMDANHPDFIANCRAHVQRLVQRDKNHPSVILWSVQNEMRWVDGRDGYKQHIPGLMKLMRDLDSTRPIMVEGDNRLLPKELTEVESRHYNIDGTISQWDRTVPLTFGEHGGWWYICPQNSSMYVGLGAYRDTDASAAGLAQKERLFVEYARRQGVSGISTFNFVHYFMRAMPDRDIALPPADLTEPGPKPVLIPAYSLSLNNGLLPEEYPAYRVNPSFDIMAEAFKPVTMIAAEYNRCFFDDSPIRRSFDVYNDTLAEQAVTIECTVQQDGRVVHTRAFSFRQEPAERRCIRLEWMPDSVDGEGEAVLAARLFHGGELKHELSLSYRLLSGSCKTAPVALELPAVYTGSDRDYEVIKVLVPDLDRIDPEAIEQLPGGILLIVGSKMPDMDGGLDRKLRGFVQQGGRLLLLEQLHLSPGKLPLVRREFIRAQAGSYEHPVLQGLGDEDLMFWHEELREEGPLPIIKAAFEKPVTGDFTLLLECSSGDFGDGGDLWSPLLEYRNGAGMFLANQLEIMDHLHRIPQACLLLRGLLRYAGRAVPAAAAPVPAAVWVRSGSPAEALLRKLRLKGTWLDSAAGLSSLSPGLLVVEAGLLNGPGAAEAVRQAASAGSRVLVLPAEPGGQEALARLLDRPVRIAPHGTYHLEADYAHAAVQGFSPVDLFGFDKVFLSPRDVVNRELALHRLEVPDAEVLCTSVEGTAWKDYFAGQHTAEYSRLALVELNRDKAREPGGFLIRIAAGEGEIICSQLLTEADSDKSLRLYTRLLGNMGAAFADELLIRDKGDAEWAVETAMVLPCPPYVDYQAMKDYYTDPEFSLNNLGEGLYGWMKKKERRADGTLLIPDPAGCPVFLSCFVHLPALSEDSRTGNVRTGRLQVQSDNAFEIYMNGEQVAAPEKEIRLSSGINRLIAIVQGGREDFAFGMVFLNSDGTYMNDLEYRLTMDEVEPK
>NZ_LN831776.1|WP_020426834.1|6949554_6952029_-|hypothetical-protein
MMKQPGPASPAGLSGSKEHKKGVVKTAGGAAVVREQQLDQYFTFRDELKEVEFKRHDMPTPWMNYLSNGTFHTMLSHAGGGVAFYKSPQIWRITRYRFFHLPTDRSGPYIYLQDAGTGRYWCPTYEPAFQKPQEWSSSHGLGYTRFEAQEDEVAAKTVYFVGPYENSLIWNLTLTNNSPAVKVLNVYAYAEFGMMEFMRELQWQCYNKHQVSVQYHPKEALVYKYGVENQPKPEETPLVYMMSDTPLHSYDGDREEFIGSYRSESNPAAIEQGGCTGSTLLGGDPCGALQVQVTLQPGETRTVNFFLGTAMDEVEVEQAIEHSREADFVARSYAALKENWDSYLGAWNCELPDADAQRMLNIWNPYQAQRNFLFSRNISFYATGTFRGVGFRDTAQDILAVAPFDPEAAKEKVRLLLGQQYQDGHVNHYFFPNEGWDPVTSIHSDDHLWTALAVWDILAETGDAGFLQESLPFYDGGEGTLYEHLKRAIDFTASRLGPNGFPLMLRSDWNDQLFRVCRQGKGESIWTAMQLGTVLLRMKDLAAASGHPEHAAGYEAMYENQKDLVNTLGWDGQWFRRAVMDDGRFLGTDEHDEAKIWLNAQTWATLSGMAEPDKAVQAMDSVRDILDTELGIKKLHPSITTFPDPADPLTNYNKGTGENGAVFCHANTWAIIAECMLGRGDQAYKYYRQLIPNVAMEQAGIWRYKAEPYVYASNLFGPESDKFGLANVSWLTGTAAWMYIAATQYIMGIKPVLEGLSIDPCIPSEWEGFTVNRRFRGCLYEISVTNSSHNCKGVKEIRVDGQRLEGNIVPAYPEKAMVKVEVIL
>NZ_LN831776.1|WP_020426833.1|6947199_6949155_-|cadmium-translocating-P-type-ATPase
MQATSKQLPKSLAREGSAQQPRTPRPRRFDPKAMLSNAEMQAALGSGLLLLIAWAVSGWSEIFSILLYIVSYSVGGWIKAKEGVETLVKERDLDVNLLMIAAALGAASIGYWNEGAMLIFIFALSGALESYTMERSKKDISSLMALKPATAVRIEKGGMSEVAIDLLAVGDQLLVRPGEIIPADGTVYRGESAVNQASITGESLPVEKSAGSDVFAGTINGEGPLYIEVTKSAENTLFAKIIKMVEEAETEVPESQRFIKRLESIYARVVVAATAALIALPPFLLDWSWSAAFYKAMVFLVVASPCALVSSIMPAMLSAISKSARKGILFKGGVHLENMAKTSVVAFDKTGTLTEGLPQVTDFIAGEGYDRTELLAVSASIEKLSRHPLAEAIVRKAEEEHLVLHVIEESTSVTGWGIEGLIEGRLWRIGKSNLLDERNEDGDEQWKTLRRQLEKEGKTVSLILDVEKIAGMIALQDTVRPQAVAAVRKLQELGVKVAMLTGDRAATAEVIAGQTGVDLVFAGLLPEDKVTHIKALRKQYGNVVMVGDGVNDAPALATATVGIGMGMKGSGAALEIADVVLMNDNIEEIASTITLARRSQRIVKQNMVFAVTVIATLMLSNFLQGIALPFGVVGHEGSTILVILNGLRLLR
>NZ_LN831776.1|WP_020426832.1|6946054_6946996_-|thioredoxin-disulfide-reductase
MYKSIIIGTGPAGLTAAIYLARANLNPLVIEGPQPGGQLTTTTEVENFPGFPDGIMGPELMDNMRKQAERFGAKFVTGWVNSVELGERPFKLNVEGMGALTTDTLILSTGATAKYLGIPGEQDNIGRGVSTCATCDGFFFRGKEIVVVGGGDSALEEAGFLTRFASKVTLVHRREELRASKIMQDRVRDNEKVAWSLNRTPLEVTSGDRGVNGIKVLNNVTGEEEFIEASGVFVAIGHHPNTAFLGGQITTDANGYIVTNPGTSETNIPGVFACGDVQDTRYKQAITAAGSGCMAAMDAEKYIESLEHSAVIL
>NZ_LN831776.1|WP_020426831.1|6945665_6945899_-|glutaredoxin-family-protein
MENVIVYTSTNCPHCRQVKSFLSEKGISYEERNIEQNDDYAQQVWDMGMRAVPVTVIGDFKIVGMNKTQFDKALANV
>NZ_LN831776.1|WP_020426830.1|6945084_6945525_-|GNAT-family-N-acetyltransferase
MLISLKNYWDRDAVERLLAECMEAGAAEIAEEVDRYLTGDSRELLGTFVNGELAGLAGIRHEPGEAIGLLHIAVQARLRGRGIGRAMIEELRRCQGNDMLRAETDLAGAGFFRKSGFVVTSLSEKDPGVERFDCVLPVSSQAEYAL
>NZ_LN831776.1|WP_167345678.1|6944354_6944516_-|hypothetical-protein
MLRNNGRNAVVEAQTVGVLRNNGGNAVVEAQTVDVFRNNGKNAVVEALEVSLL
>NZ_LN831776.1|WP_020426829.1|6944039_6944234_+|hypothetical-protein
MTYVDTSDISAQMFITVLLLLLIIAPLISLGVLRLFQSRKKSGLLLIVSGIAVYALFQIIMYFI
>NZ_LN831776.1|WP_020426839.1|6958308_6959109_+|polysaccharide-deacetylase-family-protein
MKIKLDLFPGGVTKALTTSWDDGRIYDRQLVAVLNRHGLKGSFHLNSGFFGKDSYITREEAASLYKGHEISAHTCTHPFLSMTPREGIAEEVLRDREHLEQIAGYPVRGMSYPFGDYNDGVLSILPALGIEYSRTVQSHGSFILPDNPLAWHPTCHHRDMLALGQQFLEEKPKYPRMQLLYVWGHSYEFNDNNNWEELEQFAGMMGGHEDIWYATNIEIVDYLSAVRGLRFSASRSIVYNPSAVDVWITAEDQVRQIPSGATLQLD
>NZ_LN831776.1|WP_046504599.1|6959589_6960669_-|IS200/IS605-family-element-transposase-accessory-protein-TnpB
MFVLKAHKYRIYPTHEQQQYLAKVFGCVRFIYNKMLADKIEHYKQTEKMLHNTPARYKKAFPWLKEVDSLALANVQLNLEKAYRHFFRDKNVGFPTFKSKKTNNNSFTTNNQNGTIATKAGTIKIPKLKTRIRIKVHRPFWGRIKSCTLSKTPSGKYFASVRVETDIAPLPKTEKKIGVDLGLRNFAITSCGEVIANPKHLRQSEQRLAKLQKDLSRKKKGSHNRNKARLKVAKLHEKIANQRKDFLHQTSTQMIRENQVIVMEDLRVKKMMQNHKLAKAISEVSWSMFREMLTYKSEWYGRELMIAPKHFASSQRCSCCGYKNAEVKNLAVREWTCPECSVQHDRDVNAAKNLIQLAI
>NZ_LN831776.1|WP_167345565.1|6961066_6961225_-|hypothetical-protein
MRRRHILFSSPVIQGFCYTQLTDVEQEINGLLTYDRKPKAPVERIRSIIKGE
>NZ_LN831776.1|WP_039785258.1|6961295_6963296_-|alpha-L-arabinofuranosidase
MRISMKKAMLLTLIAALLVMGISVAPVQAATTGTVISSSAAEPEPYYARAVKLDNGNLLSTFTRRFPGNTDWAGMKAFPFYRSTDGGATWSLLSEIDPNNYGLDRNQQGMTTLYVLPQKAGDYPAGTLLFASTDWNNSVPYTIHIWRSTDNGATWQFHSNLAARGTAGTQRTWEPEFSVTSDGRLICYYSDERQPGYNQAIAQEISSDGGLTWGNYSIIVGNSSNWDWRPGMPRVVKVKNGTYFMFFEMLGAAPNFAVRYKTSANGVDWGSATDLGNVVGTGIYRASQTPEIAYIDNGTANGRLYVRGMTDVISSANKMFTSGDYGATWTQVDAPLTVKGSNQNTPAAWSGTLLPLSHSMLLEVNTVKVGDRNEIRANVAQVNGDSSIVSGGIYKLINQNNNLLLDNAGGGSPAGTEIIQWSDLGADTQWWRLDYRNSGFFRGMSVNNSLVWEDPDGATAPGTKVILGTNNDLDTQRWKFAHKGSSYYTVMNGHSGLMLDNAGGGSPAGTKVIQWGANSLDTQNWKLVRVDTEIPVNQLESFNMHSYVQYQDGRGRIDGGQYSAESQWRLVKGLANESSVSIESVNKPGFYLRHRDGKVWLEANDNSALFKNDATWQLRAGLTGSWAASFESYNIPGAYMRHRNGLLEISTISTAVDQQDATFYVK
>NZ_LN831776.1|WP_020425889.1|6963341_6964295_-|family-43-glycosylhydrolase
MAGTETFRNPIVARAADPWVLRHTDGNYYFMHTQSGGLGLTQSSSLTGLAQGRKKTIWSPEPNGRYSYNLWAPEIHHLNGKWYIYFTANDGGGDESRRICVLENGEADPMEGEWVWKGALPTPVPGLDGTVVTVQEQLYFLYAGYGHYPDYGSAIYIMRMSNPWTLEGDHVLLTAPTLDWEKQGGMAINEGPVTLHRNGRIYLVYSASTTWSEDYALGILTMEESADPMEPSSWTKSPVPVFHKSVENGVYATGHNSFTVSPDGEEDWIVYHALPAPGADAGLRATCIQRFTWKEDRTPNFGIPVSADEDIAAPSGE
>NZ_LN831776.1|WP_081487080.1|6964355_6965120_-|carbohydrate-ABC-transporter-permease
MAVPFLWMLSTSLKQQGMEFEMPPKWIPQHFEWSNYHFVLFESDIVQGFVNTLLIILLPCLVGLFTSALAAYAFARLLFPARNLLFGLLLATMMIPGVVTMIPTFMLFKNIGWIDSWMPLIIPGMFGAAAAVFLLRQFFLTIPRELEDAAKVDGMNPFHTFLRIMLPLSKPALITQGLLNFIAGYNDYLGPLIYINSPEKYTLQLVLASFQGFYTSQWTYIMAGSVLALIPTLLVFFFAQKYFVEGIALTGMKG
>NZ_LN831776.1|WP_020425891.1|6965243_6966110_-|sugar-ABC-transporter-permease
MKRREYLWAYSFIAAPILGFLLFAFIPLSYSVYVSFTDYSGYQTPVFNGGDNYVKLVQDELFWKTLRNTLYSALSIPIGMICSLGFATALNQKIQGIRFFRTMFFLPTISSVIALTLLWKWIFNDTYGLLNHLLELAGIQGPAWLSSEQWAMPAMIIQGVWSGLGINIVLYLAALQGVPRSFYEAAEIDGANGWQRFRHITVPCISPTTLYILITAIIGALQDYPRFQIMTEGGPNYSTTTIVYYLFQNAFRYMNMGFASSMAWILGLIILAVTLLNFYFSRRWVHYE
>NZ_LN831776.1|WP_020425892.1|6966181_6967522_-|sugar-ABC-transporter-substrate-binding-protein
MNVSKSNSGKYLLLSLSLALLTGGLAGCGNSKKEPEAGNIPNAEGQVTIQFAGWGDPSEKEVFTNLIQAFEKANPAIKVDYLHIPSGDYVGKMNTILAGGNAPDVLYVPDGDFGRWVSQDLLLPIEDLLKNSSIDTADMWASGLERYRYDGSANGQGELYALPKDIGPHVLYYNKDIFTKMNVPFLSADTPMSMEQLLDTAKKLTVSKNGKTTQYGMGPVWWEDFVLAHGGSFLSDNKQEFVGNSQETIDALQFAADLTNKHGVVPSSSALKDLNDSEMFKTGKLAMMVSGRWMVPEFRKLNFDWDVAPLSGKGWGGISGSVGLAIYSKTKHVEAAYKLVEYLGGPEGQREQSLMGFSIPSFKSMASTDVFLQPGQKPEHAEVFIQAVEKEVSGPWTALPNAKWYDLLAQGLAPMWEGKKSAADVLNDLKPKIDAAIKEGNSGLFK
>NZ_LN831776.1|WP_046505798.1|6967672_6968536_-|AraC-family-transcriptional-regulator
MQNDTKNFVISMERFMPHTFQAEKGEGLFMSHSHEYDELTLILEGEGYYSSAEQNIKVSKGDLILIPSRLHHGFVCTEPWQGISVHFYHDKLPAYCQYLFHNAEREQDRIRSAYLSEEDMRWAEISLIQLEKEWKLESYNADSYVLMRVALETILLLFQRNRVTMLLPHVLNDQFTIQEVLKEIHAGYHTQITVSELASRYFLSESNLRKKFTELIGVSPKQYIINLRLREAKRLLQQTDKAVEIISHEVGFTSSSRFYHFFVKAAGATPLEWRKKVGEQTLTNNHP
>NZ_LN831776.1|WP_020425895.1|6968806_6968995_-|hypothetical-protein
MAYSVGEDYDPFLYSMQLLDEPKDLEGLGARVISGGVRGLFTLTEAIIMYDKQGHYWAAVSL

Crispr_ID: NZ_LN831776_71

• CRISPR_ID: NZ_LN831776_71
• CRISPR_location: 7001322-7001415
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_71

Consensus_repeat	Method
TGTTGCTCATTGTGCAGGATTCT	CRISPRCasFinder

spacers of NZ_LN831776_71

>71.1|7001345|48|NZ_LN831776|CRISPRCasFinder
CGCCAACATAGCCAACATAGTCCAACATAGCCCGATTAGAACGAATAT

CRISPR arrays and Neighbor proteins around NZ_LN831776_71

CRISPR arrays

The CRISPR arrays of NZ_LN831776_71

>merge|NZ_LN831776|71|7001322-7001415|CRISPRCasFinder
TGTTGCTCATTGTGCAGGATTCTCGCCAACATAGCCAACATAGTCCAACATAGCCCGATTAGAACGAATATTGTTGCTCATTGTGCAGGATTCT

>NZ_LN831776|71|71|7001322-7001415|CRISPRCasFinder
TGTTGCTCATTGTGCAGGATTCT	CGCCAACATAGCCAACATAGTCCAACATAGCCCGATTAGAACGAATAT
TGTTGCTCATTGTGCAGGATTCT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020429538.1|6990858_6993162_-|beta-glucosidase	unknown	unknown	gnl|CDD|185053
NZ_LN831776.1|WP_085981595.1|7005808_7006258_-|SulP-family-inorganic-anion-transporter	unknown	unknown	gnl|CDD|223732
NZ_LN831776.1|WP_020429532.1|6999847_7001128_+|glycoside-hydrolase-family-125-protein	unknown	unknown	gnl|CDD|377716
NZ_LN831776.1|WP_020429539.1|6987597_6990855_-|alpha-mannosidase	unknown	unknown	gnl|CDD|212101
NZ_LN831776.1|WP_020429521.1|7010370_7010760_-|response-regulator	unknown	unknown	gnl|CDD|381100
NZ_LN831776.1|WP_020429531.1|7001935_7002613_-|deoxyribose-phosphate-aldolase	unknown	unknown	gnl|CDD|234784
NZ_LN831776.1|WP_020429530.1|7002774_7003611_-|prohibitin-family-protein	unknown	unknown	gnl|CDD|259799
NZ_LN831776.1|WP_020429535.1|6995793_6996708_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_LN831776.1|WP_046505821.1|7006399_7007476_-|bifunctional-3-deoxy-7-phosphoheptulonate-synthase/chorismate-mutase	unknown	unknown	gnl|CDD|183614
NZ_LN831776.1|WP_020429519.1|7011798_7012344_+|glutathione-peroxidase	unknown	unknown	gnl|CDD|238207
NZ_LN831776.1|WP_039789224.1|6982956_6984066_-|amidohydrolase/deacetylase-family-metallohydrolase	unknown	unknown	gnl|CDD|236423
NZ_LN831776.1|WP_020429536.1|6994865_6995777_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_039789222.1|6984263_6986555_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_020429529.1|7003821_7005579_-|methyl-accepting-chemotaxis-protein	unknown	unknown	gnl|CDD|223910
NZ_LN831776.1|WP_046505817.1|6997063_6999823_+|alpha-mannosidase	unknown	unknown	gnl|CDD|223460
NZ_LN831776.1|WP_020429524.1|7007904_7010169_-|PAS-domain-containing-hybrid-sensor-histidine-kinase/response-regulator	unknown	unknown	gnl|CDD|236842
NZ_LN831776.1|WP_020429540.1|6986578_6987595_-|glycosidase	unknown	unknown	gnl|CDD|350126
NZ_LN831776.1|WP_020429520.1|7010907_7011582_-|DUF2294-family-protein	unknown	unknown	gnl|CDD|378372
NZ_LN831776.1|WP_020429516.1|7012882_7014166_-|ArsB/NhaD-family-transporter	unknown	unknown	gnl|CDD|238536
NZ_LN831776.1|WP_020429537.1|6993195_6994827_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270299

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020429538.1|6990858_6993162_-|beta-glucosidase	gnl|CDD|185053	PRK15098, PRK15098, beta-glucosidase BglX.	0
NZ_LN831776.1|WP_085981595.1|7005808_7006258_-|SulP-family-inorganic-anion-transporter	gnl|CDD|223732	COG0659, SUL1, Sulfate permease and related transporters (MFS superfamily) [Inorganic ion transport and metabolism].	1.32543e-30
NZ_LN831776.1|WP_020429532.1|6999847_7001128_+|glycoside-hydrolase-family-125-protein	gnl|CDD|377716	pfam06824, Glyco_hydro_125, Metal-independent alpha-mannosidase (GH125). This family, which contains bacterial and fungal glycoside hydrolases, is also known as GH125. They function as metal-independent alpha-mannosidases, with specificity for alpha-1,6-linked non-reducing terminal mannose residues. Structurally this family is part of the 6 hairpin glycosidase superfamily.	0
NZ_LN831776.1|WP_020429539.1|6987597_6990855_-|alpha-mannosidase	gnl|CDD|212101	cd10789, GH38N_AMII_ER_cytosolic, N-terminal catalytic domain of endoplasmic reticulum(ER)/cytosolic class II alpha-mannosidases; glycoside hydrolase family 38 (GH38). The subfamily is represented by Saccharomyces cerevisiae vacuolar alpha-mannosidase Ams1, rat ER/cytosolic alpha-mannosidase Man2C1, and similar proteins. Members in this family share high sequence similarity. None of them have any classical signal sequence or membrane spanning domains, which are typical of sorting or targeting signals. Ams1 functions as a second resident vacuolar hydrolase in S. cerevisiae. It aids in recycling macromolecular components of the cell through hydrolysis of terminal, non-reducing alpha-d-mannose residues. Ams1 utilizes both the cytoplasm to vacuole targeting (Cvt, nutrient-rich conditions) and autophagic (starvation conditions) pathways for biosynthetic delivery to the vacuole. Man2C1is involved in oligosaccharide catabolism in both the ER and cytosol. It can catalyze the cobalt-dependent cleavage of alpha 1,2-, alpha 1,3-, and alpha 1,6-linked mannose residues. Members in this family are retaining glycosyl hydrolases of family GH38 that employs a two-step mechanism involving the formation of a covalent glycosyl-enzyme complex. Two carboxylic acids positioned within the active site act in concert: one as a catalytic nucleophile and the other as a general acid/base catalyst.	2.50938e-136
NZ_LN831776.1|WP_020429521.1|7010370_7010760_-|response-regulator	gnl|CDD|381100	cd17548, REC_DivK-like, phosphoacceptor receiver (REC) domain of DivK and similar proteins. Caulobacter crescentus DivK is an essential response regulator that is involved in the complex phosphorelay pathways controlling both cell division and motility. It localizes cell cycle regulators to specific poles of the cell during division. DivK contains a stand-alone REC domain. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.99589e-34
NZ_LN831776.1|WP_020429531.1|7001935_7002613_-|deoxyribose-phosphate-aldolase	gnl|CDD|234784	PRK00507, PRK00507, deoxyribose-phosphate aldolase; Provisional.	9.48512e-120
NZ_LN831776.1|WP_020429530.1|7002774_7003611_-|prohibitin-family-protein	gnl|CDD|259799	cd03401, SPFH_prohibitin, Prohibitin family; SPFH (stomatin, prohibitin, flotillin, and HflK/C) superfamily. This model characterizes proteins similar to prohibitin (a lipid raft-associated integral membrane protein). Individual proteins of the SPFH (band 7) domain superfamily may cluster to form membrane microdomains which may in turn recruit multiprotein complexes. These microdomains, in addition to being stable scaffolds, may also be dynamic units with their own regulatory functions. Prohibitin is a mitochondrial inner-membrane protein which may act as a chaperone for the stabilization of mitochondrial proteins. Human prohibitin forms a hetero-oligomeric complex with Bap-37 (prohibitin 2, an SPFH domain carrying homolog). This complex may protect non-assembled membrane proteins against proteolysis by the m-AAA protease. Prohibitin and Bap-37 yeast homologs have been implicated in yeast longevity and in the maintenance of mitochondrial morphology.	1.42968e-67
NZ_LN831776.1|WP_020429535.1|6995793_6996708_-|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	9.17841e-126
NZ_LN831776.1|WP_046505821.1|7006399_7007476_-|bifunctional-3-deoxy-7-phosphoheptulonate-synthase/chorismate-mutase	gnl|CDD|183614	PRK12595, PRK12595, bifunctional 3-deoxy-7-phosphoheptulonate synthase/chorismate mutase; Reviewed.	0
NZ_LN831776.1|WP_020429519.1|7011798_7012344_+|glutathione-peroxidase	gnl|CDD|238207	cd00340, GSH_Peroxidase, Glutathione (GSH) peroxidase family; tetrameric selenoenzymes that catalyze the reduction of a variety of hydroperoxides including lipid peroxidases, using GSH as a specific electron donor substrate. GSH peroxidase contains one selenocysteine residue per subunit, which is involved in catalysis. Different isoenzymes are known in mammals,which are involved in protection against reactive oxygen species, redox regulation of many metabolic processes, peroxinitrite scavenging, and modulation of inflammatory processes.	6.51088e-91
NZ_LN831776.1|WP_039789224.1|6982956_6984066_-|amidohydrolase/deacetylase-family-metallohydrolase	gnl|CDD|236423	PRK09237, PRK09237, amidohydrolase/deacetylase family metallohydrolase.	7.34126e-172
NZ_LN831776.1|WP_020429536.1|6994865_6995777_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	3.79646e-65
NZ_LN831776.1|WP_039789222.1|6984263_6986555_+|helix-turn-helix-domain-containing-protein	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.07301e-24
NZ_LN831776.1|WP_020429529.1|7003821_7005579_-|methyl-accepting-chemotaxis-protein	gnl|CDD|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	2.64195e-43
NZ_LN831776.1|WP_046505817.1|6997063_6999823_+|alpha-mannosidase	gnl|CDD|223460	COG0383, AMS1, Alpha-mannosidase [Carbohydrate transport and metabolism].	0
NZ_LN831776.1|WP_020429524.1|7007904_7010169_-|PAS-domain-containing-hybrid-sensor-histidine-kinase/response-regulator	gnl|CDD|236842	PRK11091, PRK11091, aerobic respiration control sensor protein ArcB; Provisional.	6.19349e-92
NZ_LN831776.1|WP_020429540.1|6986578_6987595_-|glycosidase	gnl|CDD|350126	cd18614, GH130, Glycosyl hydrolase family 130; uncharacterized. This subfamily contains glycosyl hydrolase family 130 (GH130) proteins, as classified by the carbohydrate-active enzymes database (CAZY), most of which are as yet uncharacterized. GH130 enzymes are phosphorylases and hydrolases for beta-mannosides, and include beta-1,4-mannosylglucose phosphorylase (EC 2.4.1.281), beta-1,4-mannooligosaccharide phosphorylase (EC 2.4.1.319), beta-1,4-mannosyl-N-acetyl-glucosamine phosphorylase (EC 2.4.1.320), beta-1,2-mannobiose phosphorylase (EC 2.4.1.-), beta-1,2-oligomannan phosphorylase (EC 2.4.1.-) and beta-1,2-mannosidase (EC 3.2.1.-). They possess 5-bladed beta-propeller domains similar to families 32, 43, 62, 68, 117 (GH32, GH43, GH62, GH68, GH117). GH130 enzymes are involved in the bacterial utilization of mannans or N-linked glycans. Beta-1,4-mannosylglucose phosphorylase is involved in degradation of beta-1,4-D-mannosyl-N-acetyl-D-glucosamine linkages in the core of N-glycans; it produces alpha-mannose 1-phosphate and glucose from 4-O-beta-D-mannosyl-D-glucose and inorganic phosphate, using a critical catalytic Asp as a proton donor.	1.92839e-113
NZ_LN831776.1|WP_020429520.1|7010907_7011582_-|DUF2294-family-protein	gnl|CDD|378372	pfam10057, DUF2294, Uncharacterized conserved protein (DUF2294). Members of this family of hypothetical bacterial proteins have no known function.	2.62325e-15
NZ_LN831776.1|WP_020429516.1|7012882_7014166_-|ArsB/NhaD-family-transporter	gnl|CDD|238536	cd01116, P_permease, Permease P (pink-eyed dilution). Mutations in the human melanosomal P gene were responsible for classic phenotype of oculocutaneous albinism type 2 (OCA2). Although the precise function of the P protein is unknown, it was predicted to regulate the intraorganelle pH, together with the ATP-driven proton pump. It shows significant sequence similarity to the Na+/H+ antiporter NhaD from Vibrio parahaemolyticus. Both proteins belong to ArsB/NhaD superfamily of permeases that translocate sodium, arsenate, sulfate, and organic anions across biological membranes in all three kingdoms of life. A typical ArsB/NhaD permease contains 8-13 transmembrane domains.	5.53573e-139
NZ_LN831776.1|WP_020429537.1|6993195_6994827_-|extracellular-solute-binding-protein	gnl|CDD|270299	cd13581, PBP2_AlgQ_like_2, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	1.56878e-130

Protein sequences

>NZ_LN831776.1|WP_020429532.1|6999847_7001128_+|glycoside-hydrolase-family-125-protein
MNLPASITQYLSEADERLAHHPKLQQLFRNCFPNTLETTTKLLDDGTTFVFTGDIPAMWLRDSTEQVRHYIPFAKNDPELQRILRGLIARQMFYVNIDPYTNAFNETASGKHYRDTDDCNLNPWMWERKYELDSLCFVVQLAYMYWKEAEQTDIFDAACYQALTSIVNVIRTEQQHGEKSPYHFIRQTLQDTETLYNNGRGMPVNYTGLSWSGFRPSDDSCEFGYNIPSNMFAVVILGYIREIASEVYHDERLAAQAAQLRKEIDFGIRTYGIVNHPKYGKIYAYETDGYGNYSLMDDAGTPGLLSIPYIGYVGVEDAVYQNTRRFALSFDNPFYFEGKHAKGIGSPHTPGGYVWHMALSMQALTADNDEEMKELIDMLIRTDAGTGYMHEGFHPDDPSDFSREWFAWSNSLFATLISRAMEKGLV
>NZ_LN831776.1|WP_046505817.1|6997063_6999823_+|alpha-mannosidase
MTRTTAHLISHTHWDREWYMPYERHHVLLAKLMNELLETLEKDEHYRYFHLDGQTIIIEDYLQIHPEKKEILERFIREGRIVIGPWYVLQDEFLTSSEANVRNLLTGHQDAAKYGVISKLGYFPDSFGNMGQAPQLLRQADIETAVFGRGVKPTGFDNMVGELNSASYESPYSEMFWESPDGSRVLGLLFANWYSNGNEVPAGPEEAKVFWDKKLADAGKYASTPELLFMNGCDHQPVQRNLSDALETAKALYPDVDFVHSSFEQYLEALKPSLPANLVIVNGELRSQHTDGWGTLVNTASARIYLKQMNQRGQTLLEKGAEPLATLAYLASGQAYPHQLLNYAWKTLMQNHPHDSICGCSVDEVHREMTGRFEKSRHVGEAIIEESLKAISGQIGTSGVACWGASGIPVTVFNTTGWDRTGTVSVEVIAAKRYFKEGPNPAAIAEALDQLPLALDSGRLVDADGQVLACRAEDMGTRFGYELPDDQFRRPYMARTLRLTFEAAQVPPLGYKTYAWIQPPGESAGAPASPLTLTESGMANNFLAVHIREDGSYDVTDKRTGRVYEAQGIYEDYGDIGNEYVFRQPEGDVPLTTRGVPARISLVEHEAYRITYEIVHEWEIPASAEASFEEEKRKMVPFRQRKAGRSSEQAPLRIVTRVSLEAGGQGVQVTAAFNNQAKDHRLRVLFPTGLAAATHLVDSVFEAAERDINPAPDWINPSNAQHQQAFVSVSDGMTGFTVANKGLNEYEVLRDGKNTIAITLLRSVSELGDWGVFPTPEAQCLGEHTVEFALCPHAGDAVQSEAFAWAYQYQTPWFAVQTGWQQGSLPAVYQPLEWQGRTLALSAFKMSAAHEDIILRWYNLAHKEQEFTLKAHFPVEAVYASDILERRKPPEQLEEGMLRKAVGPAQIVTCALNPLHPQP
>NZ_LN831776.1|WP_020429535.1|6995793_6996708_-|sugar-ABC-transporter-permease
MKGNKTLGKRIWQNWELYLFMAPALLYFLIFHYGPMYGIQIAFKNFVPSKGITGSSWVGFDHFERFFNSYFFWDLLWNTFSISFYELAVGFPLPIILALAFNEVRNGPFKKSVQTVTYAPHFISVVVMAGMIITFLSPSSGMIVRVIEFLGFQPAEFLTDPAWFKTVYVFSGVWQSTGWGTIIYLAALSGVDPQLHEAAIVDGASRLKRVLHINLPTIVPTITIMLILNMGNILGLGFEKILLLQNSLNMEASDVISTYVYRAGLVNAQYSFSTAVGLFNSVVNVILLVTVNRIAKRTSENSLW
>NZ_LN831776.1|WP_020429536.1|6994865_6995777_-|carbohydrate-ABC-transporter-permease
MVTAMKESRGDKLFLISTYVYLCLALVVVVYPLVYILSASISSPQDVNSGAMWLFPKNVTLDGYKLVFENPKIWNGYLNTIIYTVLGTLLNLAVTLPASYALSRSDFVGRQLFMAFILFTMFFSGGLVPTYLLVKNLGLINSMGALILPVAASVWNIVVARTFFQTTIPKELQEAAHIDGCTNLKLFIRIILPLSAPIVAVMALFYGVGHWNSYFPSLIYLNDEAKYPLQMVLRQILVLQEMSAETTGAAINGEVAMAMNSKAETASLIKYGVIVVSTLPIVAVYPFLQRYFVQGVMIGSVKG
>NZ_LN831776.1|WP_020429537.1|6993195_6994827_-|extracellular-solute-binding-protein
MQKTTRKPWKLLLSGTMILTLLAGCGSSNEGEANSGTGNGKGNGNITVNKEGFPIVTEPVTLTMMAPDVGIQNWENMPVLQQMQEMTGITLEYQNAPKDSFETKKNLVFASGDYPDIFYAAGLTTAEQMNYGEQGILIPLEDLIDEYAPNFKALLEDNPDVRKSITAPDGHIYSLPVVELSQHWYRNPMWYNGDFLKALNIDKLPETTEELYTYLKRVKEEDPNGNGVADEIPISSVTTAAANLRDIRTWLLGAFGIYEEEIYVDDADKVHYTPLEEGYKEYLTYMNRLWSEELLDHESFSQTAEQKKAKAQNNRVALFSDWHAYMTKGGEQSTADPMFAPVRSESVAAPAIAKNRGITTGAFAITESNPQPEASMRWVDYLYSYEGALFFNKGPEGTLWEYTDKENRVKQYLPVPDGKEMEDFRATLTPNYGIPAPTLSMDDINKGLKTDFDLWVEQETKQKLLDKGARIPFPALFLTVEEQTEISSLNSDLSTYVKQMEAKFITGAEPLTGWDNYVATVKKMGGERVAEINQAAYDRWKSN
>NZ_LN831776.1|WP_020429538.1|6990858_6993162_-|beta-glucosidase
MIYKDKTCSVEDRVRDLLPRMTLAEKAGQLVQPFGWQCYEKRPDGTAGMTEAFKRRIASGGVGSLYGTLRADPWTGVTLDTGLSPKEGAETVNAIQAYAMKESRLGIPILFGEECSHGHMAIGATVFPVPLALGSMWNPELYREMCRAVALETRSQGGAATYSPVLDVVRDPRWGRTEETFGEDPFLIAAMGVEAVKGLQGERLDGEDSVMATLKHFAAYGSSEGGRNSAPVHMGLRELHEVDLLPFRKAVEAGALSIMTAYNEIDGVPCTTNRYLLQDVLREQWGFEGFVITDCGALGMLTSGHNTADSGEAAVAQALLAGIDMEMSGEMFEKHLSAAISHGRLKASDLDRAAARILELKFKLGLFDRPYADPERAGQVIGRPEHRALARRIAGESIVMLKNEADTLPLSKNIRRVAVIGPNADAPYNLLGDYTSPQPKGAVVTVLDGIRSALGGNPDRVLYAPGCRIKGDSREGFPHALACAAEADAVVMAIGGSSARDFGEGTIDLLTGASVVTEHSWSDMECGEGIDRSTLNLMGVQLELVQEIRKLGKPLIVVYINGRPIAEPWIAEHADAILEAWYPGQEGGHAIADILFGEVNPSGRLTISIPKHVGQLPVYYYKRRTRGKRYLESDFNAEYPFGYGLSFSEFRYSNLRVQPAVIPADGEALVSVEVTNTGTRAGSEVVQLYISDLASMITRPEKQLKGFRKIRLEPGNTQTVTFSVGREQLEYVSADLTRIVEEGEFTLMVGPHSEEYLTAPLHVREEG
>NZ_LN831776.1|WP_020429539.1|6987597_6990855_-|alpha-mannosidase
MKRINRFIDWLAERQWTERIELTEWKLRKSRYLAPGVYEHEEELHPDYKISRLDGGYGTTYFLQRQVAVPEGWAPEETALLYIGRGEGLLSINGAPYHGLDSNHWFISLPPGSTGGELTLDIELYDPVPEPEDPLNRQAVIKPPLEGVTISLVRVHLPVYSLLHTVKTAHEAALLLPEGDMRRIRTLQALEQAMDALYMKGHLLYSGDAAAGVEERLRAAVSMERSAGTSEGIMHMVGQSHIDIAWLWPIRETVRKVSRTFSTVCALMDKYPDFRYSQSQPQLYAYAKAYYPGLYERIKARIAEGRWELVGGMWVEPDLNIPGGESLVRQMLYGQGFYMQEFGKRSTVEWLPDTFGYCASLPQLLKQAGIDYFMTTKLGWNDTNPFPHTLFHWVGIDGTKIVAYQNHGVNEHTRPKDVQEHWQSNAQKDRHNELMLLYGHGDGGGGVTHEMLEYVARTDLMPGQPVSGFSTAEAFFSEIGARQPELPKWYGDLYLELHRGTFTTHAYNKRSNRKAEILYRQAEIWSVLAEQAGLLEQAEAKPKLDGGWKLMLLNQFHDIIPGTSISEVYTTSREQYAEVFSLGRQVLETSLHALASKVDTSGAGRPYVAFNSLGWERTELIRLEGDCSLAAVQAFDEEGRLDSECWSMEGDSGRYTLVVRVRKVPAFGCRVFWLREAAERGRGQAPIPAPVPALAQAQAPTPPITPEQALLESSEGAAGPVNGLAGISAGDAFPDLWETEYYILQFNEDGEISRWYDKSAGRELLPPGQTGNQLRYYHDTPPLWDAWDLDPRYEQQPAGRAELLERKVLVSGPVLTVLKFRWQLNQSLIEQEIILPRHSRRVDFQTRVSWKEEHKLLKAAFPVDIVAAKATYEIPFGALERPTHRNTSWEQAQFEVCGHRWADLSESGYGASLLNDCKYGYDIHDGVMRLSLLRSPRWPDRQADRGEHVFTYSLYPHTGDWRQAQVVRAAAELNEPLLAVSEDPHPGRYPSTYAWLGLQSGPVVLDTIKNAEDGSGIIVRLYESTGGRGTATLNWQTADIGACRVNLLECGTEPLDTAGGALTLSFKPYEVQTVKLYREHHSQEE
>NZ_LN831776.1|WP_020429540.1|6986578_6987595_-|glycosidase
MKITRHKSNPIVVPGGYEWRKVTVFNPAVIIDNGKFYMIERTAGSLTPCKNFLGLLESEDGVNFTHVKDEPIVTPDMLGFPYGSVQDPRIVKIDGTFYLNYALRPCAMSYYPTGAGVPERSIPTYPDGWGEEEGHWLTRSSILKSDNLLDWEFVADTTPLDINDRDNILFPEKIGGKFVLLRRPEEYVGEAYGTEKAAMWITYSEDLIHWEEPKLLATAGNLSWESRKIGGSAPPVRTDKGWLVLYHGVDENIVYRVGAMLLDLEQPEKIIARTHNFIMEPETYYEKFGFQIPNVIFPTGNVVKDGLLYIYYGVTDTAIALATVPLDELVEHILQEAQ
>NZ_LN831776.1|WP_039789222.1|6984263_6986555_+|helix-turn-helix-domain-containing-protein
MNWNHFKSKLLLKYAFSYILMFLIPLTGVTIFVYENAVKGLRVEIEQSNVNQLNQVKSTIDARMTELQEISGRIAYDKHLTPYMVRHPYYSLEAIQALANYKASSSIVEDLFLYFHDDANIYSYRGLADLHVTFDTLYQFEHWTPEDLRQALNETRQPLVRPAESVTVNSRKEPMLAMLVPVKPNDPFPYGTVLYLMKESKLTGVMDSILSDFSGSSYIFGAGGEVLTANSHGVSLPREELSTLSALEPGIHNLVLDGEQYSVVSVQSDENGWTYVTTMPSYQFFSRVAHVQTLILIVFCITVVTGIAAALLLAKRQYHPIKDLMEFARLGSSGNDALKTRNEWEWIRQTLHDYSARIDLQEPFVRNQCMLLLLKHGKPDDPEIEQMILSAGFRHPQEQGLYFSAILSWDDAAPGGKPWHERHLLQEILSNLCLPGPDAQIFGVEFSAKDQFALIISLPGHEAGSVQSRMEQVVEAIQTVIRDHSQLVPNIGVGMAYRDLARVNQSFIEAAAALEHRMIRRSGYVTYFEQLAERNAPAADNFWIPRKSMLKLEQSLKQGNESVAVQMIADTIDTIKDEPLQIHLLRCICFDLLNAFLRIASELGMDGVFADMPGLTSFETLEELESRLLSLAAAICGQVERNTETGESSLMDDILAYVDQQFADYTLSLEHVALKFAISTSYLSRSFKEKTGTNFSQYIWQRRVDEVIRLLENTSAPLKEIIEQVGYLDAPNFIRKFKKETGLTPGQYRKDHSLKRSVAKRPV
>NZ_LN831776.1|WP_039789224.1|6982956_6984066_-|amidohydrolase/deacetylase-family-metallohydrolase
MEQVGTENVLRNLQLVDGRTVDIAIRDGIISAITPAGRAEGKTMLDGSGLYVSSGWIDLHVHAVPELHPYGDDIDEIGVKQGVTTIVDAGSCGADRIGAFYAGSLLAATNVLAFLNISRIGLERTDELSQLEWIDRDEAVQAAAAYPDFIVGLKARISQSVVKENGIQPLKQARALSGETKLPLMVHIGSAPPEISEVLELLQPGDVITHYLNGKSNNLFHADGTPLQGLLEAVAKGVHLDVGHGTASFSFRIAGQAKKAGIPLNTISTDIYRGNRLNGPVYSMSNVLSKFLYLGYSLEEIIHAVTRNAALWLKRPELAGISVGQQANLTLFALEEGRKELTDSEGDVRVADHYIEAKGVFANGSLITC
>NZ_LN831776.1|WP_020429531.1|7001935_7002613_-|deoxyribose-phosphate-aldolase
MSTNTLSGIIDHTLLKADARKEDIIKLAEEAKTYTFASVCVNPAWVATAHEVLKDTPEVKVCTVIGFPLGASTPETKAFETTNAISNGAGEVDMVINIGALKDGDNELVKRDIAAVVGAARGKALTKVIIETCLLTDEEKVRACKLAVEAGADFVKTSTGFSTGGATKEDIALMRAAVGPDIGVKASGGVRSAEDALIMVGAGATRIGTSGGVAIAKGEQSQSGY
>NZ_LN831776.1|WP_020429530.1|7002774_7003611_-|prohibitin-family-protein
MKVEVNPKLKQVRPGKIISIVVAVLLVVIIGGNAFTSVEYGHVGLYKTFGKLNNNMLSPGIHFKIPFIQTVIQVNTQVTKAETDTSASSKDLQPVSTHVAVNYSVNKDSAYNLMNNIGGNFDGVIINPAIQEIVKEVTAKYPAEDLITRRDLVAGEISELLTKRLGRYDLVVNDINIVNFKFSDAFNQSIEAKQVAQQQALKAENDLRRVEIEAKQKIAQAQAEAESLRLKKQEVTPELVQLKQIEVQEKALEKWNGVLPSVTGGATPFVDVQSLTQK
>NZ_LN831776.1|WP_020429529.1|7003821_7005579_-|methyl-accepting-chemotaxis-protein
MFSFVRKRLIARIFCVMTAVILCIAAGNIAIQWVNTGSAVKGTISSYNMNIASHYAAQADAGRFSDFLDDPQETDLYWSLRAELDQFRQSIGARYVYFVKIDEANQPLLMIDGRPKGDPLASPINENTDMPDAAVEAVLAGENASTPLIKNPEYGDYISAYVPMRDGQGKLVGALGIDTDVAVLSTLTRDVLLQSLPLYGGILALSLAALGIMAWFVSRALRPLRTITESAGTMARGDLAEAARILHARPVKSRDEIGTAYQAMLRMSGDLNTRVEGIVSHVSTASDLLYGSSETFARNADDVLRMSETVNGKIADIYAGASSQTEGAQSSALAIDEMAQGISRISASAAFVSESAVKALEIVDSSQAAMHQMNRQMKSISLSTGQTLETALLLQSYAEEIEGALAAIRQFADQTKLLALNASIEAARAGEHGRGFTVVAGEVRKLAEGSAASVERVADLLLHIGNASASIGTQMTDVSKEVKEGARMSAESEAALLQASAAFREVAEQITDVSATAEQLSAGSEEVAATVGSMAHIAGGVSEQTRQIRELTDLQLEKIKEVYEASMTISANTSDMREAIRQVKV
>NZ_LN831776.1|WP_085981595.1|7005808_7006258_-|SulP-family-inorganic-anion-transporter
MEYLFAATVLAGILQILMGMLKRGRFITFLPQPVMTGFVNALAILIFMAQLTHFSGKGWVMYALVVLTLLIIYSVPRFTKAVPSALVSIIVVSVLSIVLHLDVRTVGDMGDITPALPVFHLPQLPFTLDTLLIIAPYSLSLAVVGLLES
>NZ_LN831776.1|WP_046505821.1|7006399_7007476_-|bifunctional-3-deoxy-7-phosphoheptulonate-synthase/chorismate-mutase
MSNVELEGLRARLDEINGQLLELISERAQVVQEIGAVKEKQGVPKFDPEREKQMLEKLVASNKGPFTSGTIRTLFKQIFSASLDLQSTDHKKSLLVARKNHAEDTVIVLPGGVTVGGPSSLMVAGPCSVESELQTRTVAAALQKAGVKVMRGGAFKPRTSPYDFQGLGMDGLRILREAATEYGLLTISEIVDPRHIEEALDYVDVIQVGARNMHNFELLKAVGEVNKPVLLKRGLSATLDEFVHAAEYIMSRGNMEIMLIERGIRTYEKSTRNTLDISAVPILKQECHLPVLVDVTHSTGRKDILIPCAKAALAAGADGIMVEVHPDPATALSDAAQQLNIDEFNTFFNEVKASGLYR
>NZ_LN831776.1|WP_020429524.1|7007904_7010169_-|PAS-domain-containing-hybrid-sensor-histidine-kinase/response-regulator
MLRQQAQGYSHFEHACKTGMIGVAFLSVNGQWTSVNPAVTSLLGFTKEQLLSQHLRELVCEDSLESYAAMVRALDAGEAPFAECAVHLSSASGARVPVQLHMTLISNPSTGEKLYYLIHIAELAAEEPADEPLSPVDKLYRQIVANISDVVYYATSDNICRYCSPSVSEVLGYDSEQLVGRDIRGLIHPDDLAALHFPEAQDFQRVQIRVLHTDGRYLWIEFTLRLIAEGTQYSVLAVGRDITERKIVEQKLQESVERYTSLKKYNHDAIISLDLEGRIINGNEKACQLTGYSIPELAGMNVGRIIGAEHLGEVIAYSKEGSPAEVNIDHIWHREGYSVEVLTTIAPIIINQETVGLYIIAKDITDQKKLLIAKEAAEKTNRAKSEFLAMMSHEIRTPMNGVIGMTDLLLEMSEPGSLQREYLDIIRQSGDTLLAIINDVLDFSKIEAGKTILHEEPFMLMPCVDSVLELLQHKADKKGLKIEVSIGPDVPEHLIGDGERLKQILLNLVGNAVKFTYTGGIKVTLRVLARAGGSVTLEFTVADTGIGIPESSRSRLFEPFYQLDHFIDRRHEGTGLGLAITRQLVEMMGGSIALDTTVETGASFVFTVKLREESGSLPDSASGTEGDEALSGERSLRILVAEDNEINQIVLRKILEKRGYSVDVAGDGLQVMEMAREQSYDLIFMDVQMPRMNGLEATQAIKETLPPDKQPVIIAVTANALKGDRELCLAAGMDEYISKPLRSEAITNIVGKFF
>NZ_LN831776.1|WP_020429521.1|7010370_7010760_-|response-regulator
MIEYKQTVLYVEDNQLNMALMHHIFKKNLPSVRLLKAETAALGLQIARQMLPDLIILDIGLPDLNGYEAMDQLKNDELTRPIPVLAISAFAQRSDIERARKTGFSGYITKPFQVKALTEAVERLLAGIA
>NZ_LN831776.1|WP_020429520.1|7010907_7011582_-|DUF2294-family-protein
MSTTELTSQLSSYAGRLLRERFGKGPESIHASIGKQCIALHIRNFIGPVERFLLNKEEEQAFRYTRELLMKSLLPELSAYLKDTMAIEVGELFYDWGIHNASGIIVALIKNDDVAIDDYAGRDEVHAQINEVSRKVQKEPVHTDSWWLGPRTLIIKREGILIPLEKELIGLGYENTLKTTKRKMEKRYLEGTTTIAPMLGKELADIYVDWDFDKDTSVIAYTFL
>NZ_LN831776.1|WP_020429519.1|7011798_7012344_+|glutathione-peroxidase
MSVYQYSARSIRGKETSLEQYKDKVLLIVNTASKCGFTPQYSDLQKLYEKYQDQGLQILGFPSNQFGEQEPGSNEEVNVFCQINYGVSFPLFEKVDVKGEQQHPLFTYLTEQAGFEGFDTTDSNGKLLHTMLQEREPAALDNDEIKWNFTKFLIDRQGNVVKRYESPVDPMDLEPAIQQLL
>NZ_LN831776.1|WP_020429516.1|7012882_7014166_-|ArsB/NhaD-family-transporter
MEQQGIWAIGIFLLTYGLIISEKVHRTVLAMLGALIMIAAGIVSQETALEHIDFNTLGLLAGMMMMVGITAETGLFSYVAVKAAKLAKGEPKRILVALVLVTALASAFLDNVTTVLLMVPVTFSITRQLRIHPLPFLLSQIIASNVGGTATLIGDPPNIMIGSAVKELTFMSFISNLTPVILIIILAYLPLFLLMFGKQLKTSPELQRSVMEMDERAMITDRKLLRRCLWVLGLTILGFFLHQAIHLESATVALAGAFLLLLLTGGEKMLHKAFASVEWVTIFFFIGLFVLVSGLVETGVIAELAGQAMELTGGNLAASSMLILWLSAIASAFLDNIPFVATMIPLIQEMGNLGIHNLEPLWWSLALGACLGGNGTLIGASANLIVAGLAAKEGYPITFMRYLKVGFPLMLLSMVISSLYIYLRYLI

Crispr_ID: NZ_LN831776_72

• CRISPR_ID: NZ_LN831776_72
• CRISPR_location: 7386941-7387015
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_72

Consensus_repeat	Method
AACAACAGCATTTCTGCCGTTATTT	CRISPRCasFinder

spacers of NZ_LN831776_72

>72.1|7386966|25|NZ_LN831776|CRISPRCasFinder
CAGCACAACCAACCCTCTGCTCCTG

CRISPR arrays and Neighbor proteins around NZ_LN831776_72

CRISPR arrays

The CRISPR arrays of NZ_LN831776_72

>merge|NZ_LN831776|72|7386941-7387015|CRISPRCasFinder
AACAACAGCATTTCTGCCGTTATTTCAGCACAACCAACCCTCTGCTCCTGAACAACAGCAGTTCTGCCGTTATTT

>NZ_LN831776|72|72|7386941-7387015|CRISPRCasFinder
AACAACAGCATTTCTGCCGTTATTT	CAGCACAACCAACCCTCTGCTCCTG
AACAACAGCAGTTCTGCCGTTATTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_039786263.1|7398549_7399245_-|molecular-chaperone-TorD-family-protein	unknown	unknown	gnl|CDD|376858
NZ_LN831776.1|WP_046507702.1|7384448_7385342_-|peptide-chain-release-factor-N(5)-glutamine-methyltransferase	unknown	unknown	gnl|CDD|236467
NZ_LN831776.1|WP_020426796.1|7382484_7383669_-|rod-shape-determining-protein-RodA	unknown	unknown	gnl|CDD|274033
NZ_LN831776.1|WP_020426789.1|7390549_7392091_+|hypothetical-protein	unknown	unknown	gnl|CDD|197227
NZ_LN831776.1|WP_046507697.1|7380238_7380994_-|stage-II-sporulation-protein-R	unknown	unknown	gnl|CDD|378205
NZ_LN831776.1|WP_020426233.1|7378224_7378797_-|hypothetical-protein	unknown	unknown	gnl|CDD|308338
NZ_LN831776.1|WP_020426795.1|7383986_7384286_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_039786279.1|7388540_7388993_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831776.1|WP_082118157.1|7389057_7390185_-|type-2-isopentenyl-diphosphate-Delta-isomerase	unknown	unknown	gnl|CDD|235465
NZ_LN831776.1|WP_020426231.1|7376603_7377257_-|TIGR01440-family-protein	unknown	unknown	gnl|CDD|377271
NZ_LN831776.1|WP_020426787.1|7393984_7394914_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_LN831776.1|WP_020426797.1|7381086_7382253_-|FtsW/RodA/SpoVE-family-cell-cycle-protein	unknown	unknown	gnl|CDD|274033
NZ_LN831776.1|WP_020426232.1|7377581_7378169_-|low-molecular-weight-protein-arginine-phosphatase	unknown	unknown	gnl|CDD|319972
NZ_LN831776.1|WP_020426792.1|7387191_7388292_-|redox-regulated-ATPase-YchF	unknown	unknown	gnl|CDD|236583
NZ_LN831776.1|WP_046507694.1|7378871_7380089_-|threonylcarbamoyl-AMP-synthase	unknown	unknown	gnl|CDD|223088
NZ_LN831776.1|WP_020426783.1|7400800_7402111_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|238045
NZ_LN831776.1|WP_020426786.1|7395010_7398208_+|efflux-RND-transporter-permease-subunit	unknown	unknown	gnl|CDD|223911
NZ_LN831776.1|WP_020426793.1|7385367_7386435_-|peptide-chain-release-factor-1	unknown	unknown	gnl|CDD|234801
NZ_LN831776.1|WP_020426788.1|7392239_7393748_-|cardiolipin-synthase	unknown	unknown	gnl|CDD|234967
NZ_LN831776.1|WP_020426784.1|7399635_7400637_+|GTP-3',8-cyclase-MoaA	unknown	unknown	gnl|CDD|234672

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_039786263.1|7398549_7399245_-|molecular-chaperone-TorD-family-protein	gnl|CDD|376858	pfam02613, Nitrate_red_del, Nitrate reductase delta subunit. This family is the delta subunit of the nitrate reductase enzyme, The delta subunit is not part of the nitrate reductase enzyme but is most likely needed for assembly of the multi-subunit enzyme complex. In the absence of the delta subunit the core alpha beta enzyme complex is unstable. The delta subunit is essential for enzyme activity in vivo and in vitro. The nitrate reductase enzyme, EC:1.7.99.4 catalyze the conversion of nitrite to nitrate via the reduction of an acceptor. The nitrate reductase enzyme is composed of three subunits. Nitrate is the most widely used alternative electron acceptor after oxygen. This family also now contains the family TorD, a family of cytoplasmic chaperone proteins; like many prokaryotic molybdoenzymes, the TMAO reductase (TorA) of Escherichia coli requires the insertion of a bis(molybdopterin guanine dinucleotide) molybdenum (bis(MGD)Mo) cofactor in its catalytic site to be active and translocated to the periplasm. The TorD chaperone increases apoTorA activation up to four-fold, allowing maturation of most of the apoprotein. Therefore TorD is involved in the first step of TorA maturation to make it competent to receive the cofactor.	4.17707e-13
NZ_LN831776.1|WP_046507702.1|7384448_7385342_-|peptide-chain-release-factor-N(5)-glutamine-methyltransferase	gnl|CDD|236467	PRK09328, PRK09328, N5-glutamine S-adenosyl-L-methionine-dependent methyltransferase; Provisional.	1.88691e-108
NZ_LN831776.1|WP_020426796.1|7382484_7383669_-|rod-shape-determining-protein-RodA	gnl|CDD|274033	TIGR02210, Rod_shape-determining_protein_RodA, rod shape-determining protein RodA. This protein is a member of the FtsW/RodA/SpoVE family (pfam01098). It is found only in species with rod (or spiral) shapes. In many species, mutation of rodA has been shown to correlate with loss of the normal rod shape. Note that RodA homologs are found, scoring below the cutoffs for this model, in a number of both rod-shaped and coccoid bacteria, including four proteins in Bacillus anthracis, for example. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan, Cellular processes, Cell division].	1.22368e-94
NZ_LN831776.1|WP_046507697.1|7380238_7380994_-|stage-II-sporulation-protein-R	gnl|CDD|378205	pfam09551, Spore_II_R, Stage II sporulation protein R (spore_II_R). SpoIIR is designated stage II sporulation protein R. A comparative genome analysis of all sequenced genomes of Firmicutes shows that the proteins are strictly conserved among the sub-set of endospore-forming species. SpoIIR is a signalling protein that links the activation of sigma E to the transcriptional activity of sigma F during sporulation.	2.92914e-68
NZ_LN831776.1|WP_020426233.1|7378224_7378797_-|hypothetical-protein	gnl|CDD|308338	pfam02659, Mntp, Putative manganese efflux pump. MntP is a family of bacterial proteins with a signal peptide and four transmembrane domains. It is a putative manganese efflux pump, since deletion of the gene leads to profound manganese sensitivity and elevated intracellular manganese levels in bacteria. Manganese is a highly important trace nutrient for organisms from bacteria to humans, and acts as an important element in the defense against oxidative stress and as an enzyme cofactor.	3.11234e-35
NZ_LN831776.1|WP_020426789.1|7390549_7392091_+|hypothetical-protein	gnl|CDD|197227	cd09129, PLDc_unchar2_1, Putative catalytic domain, repeat 1, of uncharacterized phospholipase D-like proteins. Putative catalytic domain, repeat 1, of uncharacterized phospholipase D (PLD, EC 3.1.4.4)-like proteins. PLD enzymes hydrolyze phospholipid phosphodiester bonds to yield phosphatidic acid and a free polar head group. They can also catalyze transphosphatidylation of phospholipids to acceptor alcohols. Members of this subfamily contain two HKD motifs (H-x-K-x(4)-D, where x represents any amino acid residue) that characterizes the PLD superfamily. The two motifs may be part of the active site and may be involved in phosphatidyl group transfer.	1.84354e-108
NZ_LN831776.1|WP_039786279.1|7388540_7388993_-|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	4.17387e-12
NZ_LN831776.1|WP_082118157.1|7389057_7390185_-|type-2-isopentenyl-diphosphate-Delta-isomerase	gnl|CDD|235465	PRK05437, PRK05437, isopentenyl pyrophosphate isomerase; Provisional.	2.17175e-160
NZ_LN831776.1|WP_020426231.1|7376603_7377257_-|TIGR01440-family-protein	gnl|CDD|377271	pfam04260, DUF436, Protein of unknown function (DUF436). Family of bacterial proteins with undetermined function.	4.35024e-96
NZ_LN831776.1|WP_020426787.1|7393984_7394914_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.46744e-15
NZ_LN831776.1|WP_020426797.1|7381086_7382253_-|FtsW/RodA/SpoVE-family-cell-cycle-protein	gnl|CDD|274033	TIGR02210, Rod_shape-determining_protein_RodA, rod shape-determining protein RodA. This protein is a member of the FtsW/RodA/SpoVE family (pfam01098). It is found only in species with rod (or spiral) shapes. In many species, mutation of rodA has been shown to correlate with loss of the normal rod shape. Note that RodA homologs are found, scoring below the cutoffs for this model, in a number of both rod-shaped and coccoid bacteria, including four proteins in Bacillus anthracis, for example. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan, Cellular processes, Cell division].	6.69462e-92
NZ_LN831776.1|WP_020426232.1|7377581_7378169_-|low-molecular-weight-protein-arginine-phosphatase	gnl|CDD|319972	cd16344, LMWPAP, low molecular weight protein arginine phosphatase. Low molecular weight protein arginine phosphatases are part of the low molecular weight phosphatase (LMWP) family. They share a highly conserved active site motif (V/I)CXGNTCRS. It has been shown that the conserved threonine, which in many LMWPTPs is an isoleucine, confers specificity to phosphoarginine over phosphotyrosine.	3.729e-62
NZ_LN831776.1|WP_020426792.1|7387191_7388292_-|redox-regulated-ATPase-YchF	gnl|CDD|236583	PRK09601, PRK09601, redox-regulated ATPase YchF.	0
NZ_LN831776.1|WP_046507694.1|7378871_7380089_-|threonylcarbamoyl-AMP-synthase	gnl|CDD|223088	COG0009, SUA5, Putative translation factor (SUA5) [Translation, ribosomal structure and biogenesis].	2.34918e-78
NZ_LN831776.1|WP_020426783.1|7400800_7402111_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	0.00116544
NZ_LN831776.1|WP_020426786.1|7395010_7398208_+|efflux-RND-transporter-permease-subunit	gnl|CDD|223911	COG0841, AcrB, Cation/multidrug efflux pump [Defense mechanisms].	0
NZ_LN831776.1|WP_020426793.1|7385367_7386435_-|peptide-chain-release-factor-1	gnl|CDD|234801	PRK00591, prfA, peptide chain release factor 1; Validated.	0
NZ_LN831776.1|WP_020426788.1|7392239_7393748_-|cardiolipin-synthase	gnl|CDD|234967	PRK01642, cls, cardiolipin synthetase; Reviewed.	0
NZ_LN831776.1|WP_020426784.1|7399635_7400637_+|GTP-3',8-cyclase-MoaA	gnl|CDD|234672	PRK00164, moaA, GTP 3',8-cyclase MoaA.	2.48726e-160

Protein sequences

>NZ_LN831776.1|WP_020426793.1|7385367_7386435_-|peptide-chain-release-factor-1
MLDRLQSLADRYEKLSELLCDPDVASDSKKLRDYSKEQSDLQPAFEAYAEYKNVMEELEAAKMMQGEKLDDEMKEMVKMEIEDLSSRQTALEEKIRLLLLPKDPNDDKNVIVEIRGAAGGDEAALFASDLYRMYTRYADAQGWRVELMDVNTNDLGGFKEVIFMINGRGAYSKMKFESGAHRVQRIPTTESGGRIHTSTSTVSVMPEAEEFEIEILDKDIRVDTFCSSGAGGQSVNTTKSAVRVTHVPTGIVATCQDGKSQNSNKEKALQVLRARISDMKRQEEEAKYAGERKSKVGTGDRSERIRTYNFPQSRVTDHRIGLTLHRLDQVMNGDITEIISALSIAEQAELMEKGE
>NZ_LN831776.1|WP_046507702.1|7384448_7385342_-|peptide-chain-release-factor-N(5)-glutamine-methyltransferase
MPDVQSIREAFAEASSFLDKSGCNEPQRSSQLLLEHVLGLSGAAYYMALADPFPPEARSAWEAGVTRRAAGEPVQYIIGEQEFYGRVFEVTPDVLIPRPETELLVEAILKYGAELWPDGLVAAPGGAARPLTAVDIGAGSGAISVTLAAEAPAWRVCAGDISPGALAVAGRNAQRHGTAVDLRLGDLLEPFAGMETDILVSNPPYIPGGDIAGLQREVRDHEPRTALDGGDDGLDPYRRMMEQLPLLPAPPRLVGFELGQGQAGQVAKLLRAAGHWSEIVTIDDLAGIPRHVLGIAR
>NZ_LN831776.1|WP_020426795.1|7383986_7384286_-|hypothetical-protein
MLDKPGTPDKPGTPSNPDKPGTPDNPGTPGKSGNPGKPDNKANRTSSGPLLPGGNSGHELLLGAEPLKLGWNISTYPAGVQPKLIVSGNFSTYFERNQG
>NZ_LN831776.1|WP_020426796.1|7382484_7383669_-|rod-shape-determining-protein-RodA
MLQKIKKIDGVIVIILLLLMVVSIFSIYSVTHGRDKLDGAHLRMIKFYVLGIIAFFGLTFVDYRLLVKYALYIYVTGIGILVLVSFIGKEQNGAQGWIKFGGFSLQPAELFKLILILFLAAVLVRKHKNKLQFWQDVVPLGLLTLLPFLIVISQNDLGNALSYIVILVGLLWIGNIKFTHALIGLLVMGGVAAGGIISYIHYHDEIKGFLTDIGRSHWVERFDPWLVPDEATAKASYHTKNAKLAIASGGMSGEGYMEGSSVQTDRVPYTYSDSIFVQIAEEFGFVGSALVLLLYFILIHRMILIALESKDRGGPFLIVGIVAMMLYQIFENIGAFIGLMPLTGITLPFISYGGTSLMINMASIGLVMSVRLHGQEVEEELPSPSVYTSPAKQG
>NZ_LN831776.1|WP_020426797.1|7381086_7382253_-|FtsW/RodA/SpoVE-family-cell-cycle-protein
MLQRFKKIDGVIVVVLLMLMVISILSIYSVTHGRKDDGLHIQMIKWYGVGFVAFFGLSLFDYRLLVKYAHYIYMLGVGILVVVSFVGKVKNGAKGWLEVGGLSLQPAELFKLILILALAALLVRKNKDELLFWRDVVPLSLVALLPFAVVIIQNDLGNALSYMVILVGLLWIGRIKWSHALIGLIIFGGSIFGFIYSYINYHEQMTSFLSETIGRKHFVARFDPWLVPELASSDDSYQTRNAKIAIASGGLSGEGYMQGGSVQSGKIPVLYTDAIFAQIAEEFGFVGAALLLLLFFILIHRMIMIALECRERAGPFLIIGIVAMLLYQIFENIGAYIGLMPLTGITLPFISYGGTSIVINMASMGIAMSVLLYGQDVEEDLPAPAVYF
>NZ_LN831776.1|WP_046507697.1|7380238_7380994_-|stage-II-sporulation-protein-R
MERSKTGRQDSLRVTFKYTAILICFFMILMMAWEGQKTDAAVAEATIPQDSIRLRILANSDAAGDQQVKRQIRDSIVEQMNQWVALLEDPQSLEQARTLIRGHLPELNALVARELEERGIDYGYKVELGVVPFPTKMYGGTVYPAGEYEAVRVTLGAGRGQNWWCVLFPPLCFIDAGSGDAAAPAAAKAKTVSAAAAGEGAKVKAAGDGAVTAPDTGAADAAGGEPEAPKVRFFFWELLENIWSWISGLFN
>NZ_LN831776.1|WP_046507694.1|7378871_7380089_-|threonylcarbamoyl-AMP-synthase
MKEPQDSSFAVQRRSGQIRSTRYWKLSAAGGPGVDPALYPQSEGDRQAIAEAAALLREGSTVAFPTETVYGLGADARSTAAVEAVFAAKGRPSDNPLIVHIARRSDLDRLVTEVHPSAAALIGAFWPGPLTVVLPVRPGVLSPLVTAGLDTVGVRMPDHPLALALIRAADCPVAAPSANRSGRPSPTLAAHVLEDLAGYIGGVLDGGAAGVGLESTVVQVQPDGTAVVLRPGGITAEQLAAVLGPGAVAAAPAAAEAPAAASARSPGAAQAAGDSSPAPRAPGMKYTHYAPRGALGVVRGASARRVAEAAAGLLQAAQRAGEITGLLLFEEHQALYPAGAAACVVSLGSLASPEEGARSLYAALRRFDEAGATYILAEACPDTGLGAAIMNRLMKAAGGTVIDAG
>NZ_LN831776.1|WP_020426233.1|7378224_7378797_-|hypothetical-protein
MDMGGVYAGWGQIVTIAIMAIALGMDAFSLGVGIGMKGIRLLHVLQLSLLIAFFHVLMPLLGLFTGSYVGHLLGQVTTYAAGGLLVLLGGHMVFNSFRADHSRREPVNHRTFWGMLLISLSVSVDSFSVGVSLGMFVNSITLTVLAFGACGGLMSISGLLLGRRVSRGLGDYGEALGGGILLAFGLMFIF
>NZ_LN831776.1|WP_020426232.1|7377581_7378169_-|low-molecular-weight-protein-arginine-phosphatase
MLHILFVCTGNTCRSPMAEGLLRKLAKERGIDVEVRSAGVSAISGTSMSRHAAAILRDEGIHDQILSTQLNAETVAWADLVLTLTGGHKRHLLQYFPDAVAKTYTLKEYVYDEEAVNADIRELDSLYADAELSLALGGEPKSADLQRIIEIRQRIPSFDISDPFGGPREDYELAAAEIRTALHSLLDKLESLRRL
>NZ_LN831776.1|WP_020426231.1|7376603_7377257_-|TIGR01440-family-protein
MDHVMKQDSRVNPAASNAAGDAGQPAGAELSLTAATAAVVRELSDAGKLGPGKILVVGASTSEVAGVRIGTGGALEVAQQLLEGIVQVAAEKGFHPVYQCCEHLNRSLVMERSLLEKLGLREVSAVPIPGAGGSMAAAAYRSMADPVLAETVEAHAGIDIGETLIGMHLRRVAVPFRPSLRYIGSARVNAAWSRPPLIGGERAVYRNPETSGSRSCD
>NZ_LN831776.1|WP_020426792.1|7387191_7388292_-|redox-regulated-ATPase-YchF
MALKAGIVGLPNVGKSTLFNAITQAGAESANYPFCTIDPNVGVVEVPDERLDKLTELVQPNKTVPTAFEFVDIAGLVRGASKGEGLGNKFLAHIREVDAIVHVVRCFVDENVTHVDGKVNPVSDIQTINLELILADLESLEKRIERSRKNIKGGDKKYVQEVEVLERIKEALYEDKPARSVELTDDERLIVRDLHLLTLKPVLYAANVGEDEVAAADENPYVQQVREFAIAENAEVVPISAKVEAEIAELEGEDKAMFLEELGLQESGLNRLIKAAYKLLGLYTYFTAGVQEVRAWTIRKGTKAPGAAGVIHTDFERGFIRAEVVAYDDLLAAGSMNGAKERGQLRLEGKEYLVQDGDVMHFRFNV
>NZ_LN831776.1|WP_039786279.1|7388540_7388993_-|GNAT-family-N-acetyltransferase
MDETTFQFFLSQSTRDYAEDKIKAGSWDVETAMQLSQDEMTRFLPEGLNTEGAYLYSIVETETDTQAGYIWFNVSEGRNGREAFIYDFYVFEAFQGKGYGKQTLLALDEEARKLKITRIGLHVFGQNNRAFELYKKAGFAVTDITMSKDL
>NZ_LN831776.1|WP_082118157.1|7389057_7390185_-|type-2-isopentenyl-diphosphate-Delta-isomerase
MGQIPQEESTHKISKTTGIAPQAAKPAGHQSLLPSPTTGERKIEHVRLCLNEEVGASGITAGFEHYRFRHNALPELNYDDISLRTVFLGRELRTPLLISSMTGGSAATGAINARLAEAAERRGWALGVGSIRAAIERSELAASFRVRDKAPGIPVIANIGAVQLSYGFGVEECRRAVEIAGADWLVLHLNGIQEVFQPEGNTGFADLLTRIERVCRELEIPVGVKEVGWGIDGETAIRLYGAGVAFVDVAGAGGTSWSQVEKFRSSDPVRRAAAEAFADWGIPTAQCIAEVRAASKHGALIGSGGLRHGVDAAKALALGADLAGFGRNLLGPAVASEETLDQALAQVELELRTAMFGIGAPDLAALRGTHRLIRC
>NZ_LN831776.1|WP_020426789.1|7390549_7392091_+|hypothetical-protein
MHPHNYTAPPEAPESTNANGHNPVPHYRKRSHHRRRKWILWMIGLLMLWLAGVMVYQTHKPLPAGISYESPVYTADRVYFWHDLTYQDQNGNQQREEQILPRILQIIAESRQFLVIDLFLFNNYTHKDQQFPAVSQELTDRLVAQQAAYPDMEIVFITDEVNTNYGSAPNPLLEQMKAAGIKVILTDVDPLRDSTPVYSAVWRTFIQWFGQSGVGWIPNLMASGGPDITARSYLKLLNVKANHRKVVVSEKTALISSGNVHDASAYHSNIALEVQGPIIADILKTEQAAADLSAAGPILSKLPEVTGENTAQTGSPLEMRYLTEGKIYKYALQGIRSAGQGDTLWMGMFYLADDRILDELVKASARGADIRLLMDPNQNAFGRDKIGIPNRPAAMDLNKRTGGKIAIRWYNTGKEQYHTKLMFIAKASGPSIVLGGSTNYTARNLDDYNLENNLWIALPKTQPLYAEMESYFNRLWGNKDAQYSLPLEAYQSDVTWMKYVLFRMQKNLGFTTF
>NZ_LN831776.1|WP_020426788.1|7392239_7393748_-|cardiolipin-synthase
MRRGLQAIVIIAALLAFYYFGFGLLGSTVGTIVSVFSTLTVISIGLGIFMENRNPSTTMSWILLLALIPVVGLILYFLFGQNVFKRRKYDKKAQRDQMAYERIENDALRMHQDWSIFDTTRQKLLGLSQRLARTPISFNSETRILTNGEETFGTLLLELRQAQHHIHMEYYIFRADHIGTRIQQILIEKARAGVAVRFMYDAVGSIQLSRAFLKELSDAGVQVAAYGNSTSFFSSRVNYRNHRKIVVIDGDVGFMGGLNVGDEYLSRSKTYGFWRDTHMLLRGEAVRTMQIIFLQDWMHTTGEKILEQDYLSPQLRFTNGDGAVQIIASGPDNERRALKNIFFSMITSAEKSVWIATPYFIPDEDILTALRVAAMSGLDVRLLFPAKPDKWLPFLASHSYFPALLESGVKIYEYEKGFIHSKLLITDGEIATIGTANMDMRSFHLNFEVNALLLQTESVSRIVADFERDLLSTRQIVHETFMNKRLLERVLESAARLMSPLL
>NZ_LN831776.1|WP_020426787.1|7393984_7394914_+|TetR/AcrR-family-transcriptional-regulator
MAADKTTDKKEQIIKTAMQLFAVKGSSSTSMQEIAELCGISKGSLYLVFKSKEELERSIYIYCFRMIRDPLQQEEQNSSRTPREKLRNQIEILLHHVYELREFFQRQFQELAGKGMTDAPEWLRKINGPLLKWSQNKLETLYGKEVLPYTGELFLLGHGMIHSYIFLLFNHESFVSIPRLANHLVDVLDIVVAGLHAGRPAPLFSSIALESWMENYEAGSHRNPLQLLKEMKERLHAGSGADPHSTEDALESIAILESEILMPHPRKAIILGMIGNLQSYPAVHPQLEDLKKLCSFHMQGVCGFHEPGI
>NZ_LN831776.1|WP_020426786.1|7395010_7398208_+|efflux-RND-transporter-permease-subunit
MKSLINFSLRNKFAIWLLTIIIVFAGLYSGLTMKQETLPNISIPYLSITTIYPGAAPEGVVNDVSKPLEQKLRNVDGVKTLTSNSLENASSITIEFDYGTNLDNATAAVREALNEVALPDNVQKPQISRFSLSSLPVISLSLSDNSSSDLESLTRIAENDIRPALEDIEGVASVQIAGQYVKEVTLKFNQDKLKQYGLTEDTIKGIVQGSSLRVPLGLFTMEESQKAVVVDGNVTTVDDLKNLSIPVVPSGAAGAGAAGGAPASAGTPAGTGAAGGAGATGAPGNAAGNAAGGAAMTGLPTVKLGELANIEVTGKSESISRTNGKESIGIQIVKANDANTVDVVNGVKDKTDELKKQYKSMDLTVLLDQGKPIEDSVNTMLSKAAFGALFAVLIILLFLRNIRSTIISIISIPLSLLIAVLCLRQMDITLNMMTLGAMTVAIGRVVDDSIVVIENIYRRLSLSGEKLRGRELISAATREMFVPIMSSTIVTIAVFLPLAFVSGMVGELFLPFALTMVFALLASLIVAITLVPALAHSLFRNGLKKGKNSHSEKPGRMAAGYQKILDWSLSHKLITFGVAVLLLVGSLFLIKPIGVSFMPSQEEKNVMLTFSPKAGQTLEDVKEQGLKAEKYILAQKHLDKMQYSIGGGGPFGMGSGNSGLFYVTYDSDTPDFDTVKENLIEGLTKEVPDGVWGDMSGMSGGGLGGNTLTVNIFGDSLDQLKPVADEIAGIVQADTGNFKDGKTSLSEAYDQYTIVADQAKLSSLGLTAGQIAMKLSPAGTRPVLTEVAMDGKNYNVYIETDKDTYSSIQEMEKATLTSPLGITVPIGEVAKIENGTSPDSITREDGKMKVDVTAEIISSDVNSASNSVKEKIDALDLPDGVTVTFGGVTEQINDTFGQLGVAMAAAIAIVYFVLVVTFGGGLAPFAILFSLPFTVIGALVALLLAGETLNVSALMGALMLIGIVVTNAIVLIDRVIHKEKEGMSTRQALLEAGATRLRPILMTALATIGALLPLVSGLENSAGIISKGLGVTVIGGLVSSTLLTLVVVPVVYEFLMKFRSKKVYE
>NZ_LN831776.1|WP_039786263.1|7398549_7399245_-|molecular-chaperone-TorD-family-protein
MTIPTVPSLVVPEAFSRWLESRGLIYQLLVDFYGRKPSLSLVAQWIRNRQLGVAAEMTEGGRELKRYLCSQEPSALPQICERETHEYMRLMNERAASTIVAREAAELGREEEFCNVLSDVYASAGIVFKKCGGEADDHISIELEFMAVMHERMLYNSFSIRSAMELLEIQERFLEEHLLRWTPQFCERLNAATDSPLYLGLSHMLEEFLPQDLQMLRAWKTSLESSAATMA
>NZ_LN831776.1|WP_020426784.1|7399635_7400637_+|GTP-3',8-cyclase-MoaA
MEPLTDPFGRLHDYMRISVTDRCNLRCIYCMPAEGMQFQPQDEIMSYEEITAVVKALAPLGLSKIRLTGGEPLVRKDLDKLVSMIAAIPGIEDISLTTNGLMLPAKAALLKQAGLSRVNISLDSLRQDRFAMITRGGEVAKVLKGIEAAEAAGLSPIKLNVVLMKGINDDEIKDFISLTLNSPLNVRFIEYMPIGSASDAWRQTYLPLETVVEACHEAGWATEEADMPSGNGPSQNRRVVGARGTFGLIHPVSEHFCDNCNRLRLTADGHIKACLYWADEYNVRPLTSDPAAVQALFRQALGNKPHNHEMALALERKAQSHTPTVRRMSQIGG
>NZ_LN831776.1|WP_020426783.1|7400800_7402111_-|helix-turn-helix-transcriptional-regulator
MEHTVTIRDELWAYLAQEELSINRFAALSGIHSGTLSRIMKGRQAMAMSHLERITQTMGLAEDYFYSKYVNECLYDSAPTWRRLRPFILRSAQLERLDCIEQLVHGLLDNLVYAPLLFDLAEELFQQDKHQAAAIIYENVAASEKYQHSERLALCQYRLFMISLGDDPQQNLIEATLFENYVNRLDEAHQLDAIKKLVHVYYSLHHWEKAEELTQELHRLASIQYNLRSRANHKHNNTTALERPLYFYILYAQLMRSCTYEERGDYKTALEIVPLYTDGSWIQEEGEEVNRIVAQFKEWGTANTYLNRLMDGQKEVLDEYVDFVSKRENEIFTALYKIVETANRYHWDVDHILKRFSSYIPYRRYSGIFTKRDKHVTDDHHARFRSELATYYLARRRFGAKEIAMRSVDLSAEVDHDRNVIKGTISVDFEINIAST

Crispr_ID: NZ_LN831776_73

• CRISPR_ID: NZ_LN831776_73
• CRISPR_location: 7412859-7412932
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_73

Consensus_repeat	Method
AAGTGGAAAAAGGGTAACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_73

>73.1|7412882|28|NZ_LN831776|CRISPRCasFinder
TGCCCAAGCACCCTGTTGTCCGCAGGTT

CRISPR arrays and Neighbor proteins around NZ_LN831776_73

CRISPR arrays

The CRISPR arrays of NZ_LN831776_73

>merge|NZ_LN831776|73|7412859-7412932|CRISPRCasFinder
AAGTGGAAAAAGGGTAACTAATTTGCCCAAGCACCCTGTTGTCCGCAGGTTAAGTGGAAAAAGGGTAACTAATT

>NZ_LN831776|73|73|7412859-7412932|CRISPRCasFinder
AAGTGGAAAAAGGGTAACTAATT	TGCCCAAGCACCCTGTTGTCCGCAGGTT
AAGTGGAAAAAGGGTAACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020425555.1|7421624_7422857_+|MFS-transporter	unknown	unknown	gnl|CDD|340893
NZ_LN831776.1|WP_020425563.1|7410054_7411920_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224055
NZ_LN831776.1|WP_020425566.1|7407645_7408389_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|187620
NZ_LN831776.1|WP_020425564.1|7409447_7410125_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_LN831776.1|WP_020425567.1|7407006_7407612_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|380062
NZ_LN831776.1|WP_020425558.1|7417409_7418249_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_085981492.1|7408385_7409408_-|HAMP-domain-containing-sensor-histidine-kinase	unknown	unknown	gnl|CDD|274368
NZ_LN831776.1|WP_046507719.1|7402673_7404014_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|238045
NZ_LN831776.1|WP_020426782.1|7402197_7402377_-|aspartyl-phosphate-phosphatase-Spo0E-family-protein	unknown	unknown	gnl|CDD|378175
NZ_LN831776.1|WP_020426049.1|7423422_7425129_-|glutamine--tRNA-ligase/YqeY-domain-fusion-protein	unknown	unknown	gnl|CDD|235424
NZ_LN831776.1|WP_020425560.1|7415154_7416447_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|227095
NZ_LN831776.1|WP_051010590.1|7416466_7417417_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_144412162.1|7405231_7406731_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl|CDD|224089
NZ_LN831776.1|WP_020425704.1|7404246_7404864_-|amino-acid-transporter	unknown	unknown	gnl|CDD|224198
NZ_LN831776.1|WP_020425556.1|7419693_7421262_+|glycosyl-hydrolase-43-family-protein	unknown	unknown	gnl|CDD|350115
NZ_LN831776.1|WP_020426050.1|7425359_7425605_+|DUF2164-domain-containing-protein	unknown	unknown	gnl|CDD|378315
NZ_LN831776.1|WP_020425562.1|7412012_7412675_-|molybdenum-cofactor-guanylyltransferase	unknown	unknown	gnl|CDD|133000
NZ_LN831776.1|WP_020425557.1|7418313_7419666_+|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_LN831776.1|WP_167345686.1|7422977_7423388_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425561.1|7413359_7415162_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020425555.1|7421624_7422857_+|MFS-transporter	gnl|CDD|340893	cd17335, MFS_MFSD6, Major facilitator superfamily domain-containing protein 6. Human Major facilitator superfamily domain-containing protein 6 (MFSD6) is also called macrophage MHC class I receptor 2 homolog (MMR2). It has been postulated as a possible receptor for human leukocyte antigen (HLA)-B62. MFSD6 is conserved through evolution and appeared before bilateral animals. It belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	6.50704e-54
NZ_LN831776.1|WP_020425563.1|7410054_7411920_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	2.44233e-174
NZ_LN831776.1|WP_020425566.1|7407645_7408389_+|SDR-family-oxidoreductase	gnl|CDD|187620	cd05362, THN_reductase-like_SDR_c, tetrahydroxynaphthalene/trihydroxynaphthalene reductase-like, classical (c) SDRs. 1,3,6,8-tetrahydroxynaphthalene reductase (4HNR) of Magnaporthe grisea and the related 1,3,8-trihydroxynaphthalene reductase (3HNR) are typical members of the SDR family containing the canonical glycine rich NAD(P)-binding site and active site tetrad, and function in fungal melanin biosynthesis. This subgroup also includes an SDR from Norway spruce that may function to protect against both biotic and abitoic stress. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	3.02799e-116
NZ_LN831776.1|WP_020425564.1|7409447_7410125_-|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	2.9278e-80
NZ_LN831776.1|WP_020425567.1|7407006_7407612_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|380062	pfam17935, TetR_C_27, Tetracyclin repressor-like, C-terminal domain. This is the C-terminal domain present in putative TetR transcriptional regulators.	1.97294e-20
NZ_LN831776.1|WP_020425558.1|7417409_7418249_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	8.51304e-78
NZ_LN831776.1|WP_085981492.1|7408385_7409408_-|HAMP-domain-containing-sensor-histidine-kinase	gnl|CDD|274368	TIGR02966, Phosphate_regulon_sensor_protein_PhoR, phosphate regulon sensor kinase PhoR. Members of this protein family are the regulatory histidine kinase PhoR associated with the phosphate ABC transporter in most Proteobacteria. Related proteins from Gram-positive organisms are not included in this model. The phoR gene usually is adjacent to the response regulator phoB gene (TIGR02154). [Signal transduction, Two-component systems].	8.2134e-66
NZ_LN831776.1|WP_046507719.1|7402673_7404014_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	0.00293923
NZ_LN831776.1|WP_020426782.1|7402197_7402377_-|aspartyl-phosphate-phosphatase-Spo0E-family-protein	gnl|CDD|378175	pfam09388, SpoOE-like, Spo0E like sporulation regulatory protein. Spore formation is an extreme response to starvation and can also be a component of disease transmission. Sporulation is controlled by an expanded two-component system where starvation signals result in sensor kinase activation and phosphorylation of the master sporulation response regulator Spo0A. Phosphatases such as Spo0E dephosphorylate Spo0A thereby inhibiting sporulation. This is a family of Spo0E-like phosphatases. The structure of a Bacillus anthracis member of this family has revealed an anti-parallel alpha-helical structure.	5.15108e-08
NZ_LN831776.1|WP_020426049.1|7423422_7425129_-|glutamine--tRNA-ligase/YqeY-domain-fusion-protein	gnl|CDD|235424	PRK05347, PRK05347, glutaminyl-tRNA synthetase; Provisional.	0
NZ_LN831776.1|WP_020425560.1|7415154_7416447_+|response-regulator-transcription-factor	gnl|CDD|227095	COG4753, COG4753, Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain [Signal transduction mechanisms].	1.94518e-77
NZ_LN831776.1|WP_051010590.1|7416466_7417417_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.1262e-80
NZ_LN831776.1|WP_144412162.1|7405231_7406731_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl|CDD|224089	COG1167, ARO8, Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs [Transcription / Amino acid transport and metabolism].	1.72552e-120
NZ_LN831776.1|WP_020425704.1|7404246_7404864_-|amino-acid-transporter	gnl|CDD|224198	COG1279, COG1279, Lysine efflux permease [General function prediction only].	1.40546e-60
NZ_LN831776.1|WP_020425556.1|7419693_7421262_+|glycosyl-hydrolase-43-family-protein	gnl|CDD|350115	cd09001, GH43_FsAxh1-like, Glycosyl hydrolase family 43 such as Fibrobacter succinogenes subsp. succinogenes S85 arabinoxylan alpha-L-arabinofuranosidase. This glycosyl hydrolase family 43 (GH43) includes mostly enzymes that have been annotated as having beta-1,4-xylosidase (beta-D-xylosidase; xylan 1,4-beta-xylosidase; EC 3.2.1.37) activity. They are part of an array of hemicellulases that are involved in the final breakdown of plant cell-wall whereby they degrade xylan. They hydrolyze beta-1,4 glycosidic bonds between two xylose units in short xylooligosaccharides. These are inverting enzymes (i.e. they invert the stereochemistry of the anomeric carbon atom of the substrate) that have an aspartate as the catalytic general base, a glutamate as the catalytic general acid and another aspartate that is responsible for pKa modulation and orienting the catalytic acid. This subfamily includes the characterized Clostridium stercorarium F-9 beta-xylosidase Xyl43B. It also includes Humicola insolens AXHd3 (HiAXHd3), a GH43 arabinofuranosidase (EC 3.2.1.55) that hydrolyzes O3-linked arabinose of doubly substituted xylans, a feature of the polysaccharide that is recalcitrant to degradation. It possesses an additional C-terminal beta-sandwich domain such that the interface between the domains comprises a xylan binding cleft that houses the active site pocket. The HiAXHd3 active site is tuned to hydrolyze arabinofuranosyl or xylosyl linkages, and the topology of the distal regions of the substrate binding surface confers specificity. It also includes Fibrobacter succinogenes subsp. succinogenes S85 arabinoxylan alpha-L-arabinofuranosidase (Axh1;Fisuc_1769;FSU_2269), Paenibacillus sp. E18 alpha-L-arabinofuranosidase (Abf43A), Bifidobacterium adolescentis ATCC 15703 double substituted xylan alpha-1,3-L-specific arabinofuranosidase d3 (AXHd3;AXH-d3;BaAXH-d3;BAD_0301;E-AFAM2), and Chrysosporium lucknowense C1 arabinoxylan hydrolase / double substituted xylan alpha-1,3-L-arabinofuranosidase (Abn7;AXHd). A common structural feature of GH43 enzymes is a 5-bladed beta-propeller domain that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	4.87603e-146
NZ_LN831776.1|WP_020426050.1|7425359_7425605_+|DUF2164-domain-containing-protein	gnl|CDD|378315	pfam09932, DUF2164, Uncharacterized conserved protein (DUF2164). This domain, found in various hypothetical prokaryotic proteins, has no known function.	1.35562e-23
NZ_LN831776.1|WP_020425562.1|7412012_7412675_-|molybdenum-cofactor-guanylyltransferase	gnl|CDD|133000	cd02503, MobA, MobA catalyzes the formation of molybdopterin guanine dinucleotide. The prokaryotic enzyme molybdopterin-guanine dinucleotide biosynthesis protein A (MobA). All mononuclear molybdoenzymes bind molybdenum in complex with an organic cofactor termed molybdopterin (MPT). In many bacteria, including Escherichia coli, molybdopterin can be further modified by attachment of a GMP group to the terminal phosphate of molybdopterin to form molybdopterin guanine dinucleotide (MGD). This GMP attachment step is catalyzed by MobA, by linking a guanosine 5'-phosphate to MPT forming molybdopterin guanine dinucleotide. This reaction requires GTP, MgCl2, and the MPT form of the cofactor. It is a reaction unique to prokaryotes, and therefore may represent a potential drug target.	2.58872e-56
NZ_LN831776.1|WP_020425557.1|7418313_7419666_+|sugar-ABC-transporter-substrate-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.9759e-66
NZ_LN831776.1|WP_020425561.1|7413359_7415162_+|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	2.66204e-55

Protein sequences

>NZ_LN831776.1|WP_020425562.1|7412012_7412675_-|molybdenum-cofactor-guanylyltransferase
MPQFSGILLSGGYSRRMGRDKALLGLGGRPVIARLADELSKVAAGPVIACGEQEREEYRFLGLTQVPDLYPGCGPLAGLHAALLQSPTEWSVVAACDLPFASAEFMRYMMSSAAEPGRDLIRNYSGGSLQIDAAVPESITGRVQPLLGLYHKRVLPVLEEALHGRRFRVMECLDALEVLYIPEAGFTGGPEPSPLYNMNTPEDYAAALELVSTPADDSSV
>NZ_LN831776.1|WP_020425563.1|7410054_7411920_-|ABC-transporter-ATP-binding-protein
MNNKQSDKKQGASLKSFLKLLHSTKPSYGLLAFAVALSMISTLVGLVIPMFTKNLVDGFSLASVSKLQIAGIAGAFIAQTIAGGVSIYLLNYVGQKAVAGLRDRLWRKFLVLPVAYYNDNRTGESVSRMTNDTGIIKTLISEHLASLFTGVISIVGSIAVLLYLNWQMTLVLFTVLPLSALILVPLGRQMYKISKGTQDETASFTATLSGVLSEIRLVKSSGAEQKEYEAGRTGIMNLLSFGIREGKISAMISPLVSFVFMMLLVVVIGYGGMQVSSGALTAGELVAFILYLIQIVMPLTQLTQFFTQIQKAKGASERIIETLAADEEIYEGVEEAKSAEEPIVIDDLSFGYTTGDPVLSRVSFSMLPGQVTAIVGPSGGGKTTLFSLLERFYEPQSGGIKLGAKPISTFSLRSWRKLIGYVSQESPLLSGTIADNLAYGLNREVGVEELRRAAAMAYADGFISELPHGYDTDVGERGVKLSGGQRQRIAIARALLRDPKILMLDEATASLDSQSEAVVQKALSNLMKGRTTIVIAHRLATVVNADQIIFMEKGRITGRGTHEELLREHELYREFAEQQLQLNSPVLSGGGEEKGEAKNGQNPGSGRRSAHPRIGGSLFES
>NZ_LN831776.1|WP_020425564.1|7409447_7410125_-|response-regulator-transcription-factor
MAKILVVDDDPHIRELVEVFLRAEGMEEVFGASDGIEALRLLEDNGVDLAVIDVMMPNMDGWELCKELRRSYDIPILMLTAKGETSQIVKGFELGTDDYLVKPFEPPVLIARVKALLKRYQISAAQSVNVGGLRMNRKTYEVTADQGSITLPLKEFELLFKLASYPGQTLTRDRLIEEVWGYDFEGNERTLDVHVGRLRDRFPREDYGFAIRTVRGLGYRLEVGK
>NZ_LN831776.1|WP_085981492.1|7408385_7409408_-|HAMP-domain-containing-sensor-histidine-kinase
MGITIVIAGFYFSWNGGYFGLKLLEKHFNWSLTPYKSQLLTMMLQFLILFLLAGIAGLVGRLRGDERAFYIPIITAMRQISKGNFKVELENDRRYGQFGSIVEGINEMASELSRMETMRQDFISNVSHEIQSPLTSIRGFARALRDEGLSAESRAHYLDIIEAEGSRLSGLSDNLLKLSALEAESFPFERTAYRLDKQLQEMILACEPQWLDKNIDVEAELEEVTVQAVKDLLSQVWTNLLHNSIKFTPQDGMITVRLRTLDNRVEVEIKDNGIGIAEDDLPRIFERFYKVDKARSTSGGGSGLGLSLVKKIVDIHEGSITITSRPGEGTACVVVLPMQP
>NZ_LN831776.1|WP_020425566.1|7407645_7408389_+|SDR-family-oxidoreductase
MSQSLQGKVAIVTGSSRGIGRSVAERLAQEGASVVINYSSSPKQAEEVVQGIQAQGGSAAALQADISKPAQIEQLYKDTKALFGKIDIVVNNAGIMINSLIGEATEEQFDKQFAINVKGTYFSCQQAFFHLEQGGRIINFSTSVNGQMFPAYSIYAGTKGAVEQFTRQLAKEFGSKGITINAVAPGPVATDLFLEGKSEAQLEGLKKTNAFGRLGQPEDIAGVVSFLAAEQSGWITGQTLRVNGGFI
>NZ_LN831776.1|WP_020425567.1|7407006_7407612_+|TetR/AcrR-family-transcriptional-regulator
MSKSSSFLSKTEIMDAAEQTLRRFGPDKTSVTDVAKLLGVSHGTLYRHFPSKAALREAVTERWLEEQIVVPLEQIVKAPADNALAQLKVYIARLIELKRHYAEQDREMFKMYTDVTMEAAELIEVHIQRIMEQMGILIDRGIQQKRIAQSAATSSLARSLFHATSRFHHPVHAHEWRSASIEQEFEQLWQLLEQGLTASIH
>NZ_LN831776.1|WP_144412162.1|7405231_7406731_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MDKIRSGAWPPGMRLAPQRELCRQLGVNRSTVVTALGELSALGLIEGRRGGGTRVADLRAAAADGAVSYGDGVATSGSRAASYGNGMATSGDGAGTDILPVQPAGSWNSYVEEGVHYPNLPTVQDINRLEYEQGLIRLGTGEPSPGLLPGEAMTRVLAELSRQTLPPLSYEAPLGSLGLRRAVSSELAKNGIQADPDSILITSGALQGLQLIAVGLLPRGSTILLEKPSYLYSIHAFQSAGVKFNGLPMDEHGLLTDRLAREARRTKAAMLYSIPSFHNPTGILMDAQRRQKLMGVTGGLGLPILEDGAYQELWLDTPPPLPLKALDREGRVLHLGTLSKSASPGLRIGWIVGPEPVVRRLADIKMQTDYGASSLSQLAAARWLEGGYHEEHLQRLRARLRQRRDAALALLQRHFAGLAAWNVPAGGFYIWLALDKPVPLRTLFRAAHKAGLLLNTGDLYDRSDSRHLRLSYVYASPAELETGLPILAGLIRKLQRPGS
>NZ_LN831776.1|WP_020425704.1|7404246_7404864_-|amino-acid-transporter
MLEAIVHGILLAFGLILPLGVQNIFVFNQGALQPRFRRVVPVVLTAAVCDTLLIAAAVGGISLVLLSVEWVTPIVYGAGILFLCIMGWKIWNAAPGERDREARVLSLKGQVGYALSVSLLNPHALLDTVGVIGTNSLQYTGAERWAFAAAAAGISWMWFLSLAAAGRVLGRLDSSGRVIRLLNTVSALLIWGIAVYMGVRLWRSF
>NZ_LN831776.1|WP_046507719.1|7402673_7404014_-|helix-turn-helix-transcriptional-regulator
MSINQFADRCGINSGTLSRIVKGNQPIAMSHLELLTKGMGKGEDHFFSLYVDECFYYSAPTWRRLRPFMIRCAELGRMDCIERMVQILLDNLNNVPTLFEVAEGLFKQGQWQAAALLYENVSASEKYQYSERLAMCQYRLFRIALGDDQSENLRAATLFEPYVPRLDEADQLDALRHLAHVYGSLHKWCKVEELAQEMLHLAKIRYDLKGHSAQKYDNEKTSERPLYFYILYAYLMRSNVYKERGDYKTALELVPFYTDGSWIKENDEEVQRTLLQFREWGKANTYLYRLLEGQAEVLDEYVEYISSQSGEIFIALYNIIKSANCFHWKVDHILERFSGYIPLISHQTYVTELGDYNQQIMSDQYARFLTELAAYSLQHKRKEGIRYILESLESSTKINNESNIIKCVDLFEQYRSIAEDDEKRKYKSLIREVQESNGKKTTISFL
>NZ_LN831776.1|WP_020426782.1|7402197_7402377_-|aspartyl-phosphate-phosphatase-Spo0E-family-protein
MNNAVLIRIRIDWVRRKLYQMQMQYGGFSHPKVLRQSVELDKLLNNYSNIHMNQRRAPA
>NZ_LN831776.1|WP_020425561.1|7413359_7415162_+|sensor-histidine-kinase
MKRYLVDRPIQSKLLICFLPILVLSVVLTGFFSYLSSSRQLKENAFYALSDTTHQTALFMNDKFMTIFEQLVRLERNDALGNILSGEGQTAEQHRYDDLIELHKQLDDVYHSYFQMIDSIFVAFNNGRSFNLQQEYVPRKVHIDLGDWLKRYNTSKKGYYWLNSHKDTVFETVEQRKVMSSFKIIGTESSPVSGIVLINLRESYFLDIMENVNISPGGTLVLISPEGALFSKELDKGYELSGDTITALRNSTASSGSFSTDSKEGRKMAIAYNTLPLNHWVLAAVVPEKDILEGANRIKYITLVIMVFILIVVSLAAAVVARNLSNPLRYLSKQVKRFERGDFTVSFALDQHNEMGVLARGLSGLLASVVQLLDKVRSEQEKKRQIELQAMQAQIQPHFLYNTLSSIKHLIDMNERQRASTMVSALTSYFRISISKGREIIPVREEMEHVRSYLMILNIRYSQEFDYEINVADELLELPILKLTLQPIVENAIYHGIKNKHGQGHLSVTGYREGDNAVFEVYDNGHGISEAKLSQLRASLQSDTAAYEAITYGLWNAHMRIVLHFGSSYGLQLDSEEGVYTRVKVYLPYANEAKGESTDA
>NZ_LN831776.1|WP_020425560.1|7415154_7416447_+|response-regulator-transcription-factor
MLKLLIVDDDKWIREGLRANVNWSREGIEVVATAANGEEGWELVQKLRPDILLTDIQMPLLDGLQLAEKVNERYALTKIIFLTGYDDFSYAKKALDLQASGYILKYEDNEVILQSVAGTGNNLRREKRELEKARKSQSLIENKFFADLLSGVPSVDWARREMELLGIQSEGPYFRVAVIQPEDLQRFSRPGIMENTELLLFSIQNICAELFTSRLPKPFFVPYNHRINIIFNLADTDGASSSGCSLATLLEDIRHTIETCLKIPVSIGVGTVCEGFGQIPQSYNKALTAAHMKDVAGRPGLFFCDELSHSQHSHHTLLKQMESYIHKNYADENLSLAAIAGEIHISPSYVSTLFKKYREINVIEYVIRIRMEKAAELLKQTDCKSYEISEKVGYGNPQYFSVLFKKHFGMSPSDYRKSQRDELSKKTNNL
>NZ_LN831776.1|WP_051010590.1|7416466_7417417_+|sugar-ABC-transporter-permease
MRLLDYDCSGGAVMEITRQRKRKKGEAWIPYLLIAPTVLLIAGILIFPIFRVFDLSVQSYDFTRLQDAGYIGLENFRHIFTEDDLFYSTLVTTLKWVFSEVALQLVFGLIVALLLNQSFRLRGLVRSLVLVPWAVSGVLTTMLWSLMFNQHIGIINDILLKLGIIHEKIAWLANPDTVFGSVVFAELWRGIPFFAITLLAALQTIPHEVYESCEVDGAGKLKKLFHITLPYLKESIIFATLLRAIWEFNSIDMIFTMTNGGPMDMTTTLPIYMMKTSILEGNYGYGSALGVVTFLFLMIFVILYLKLNRAGGMQDE
>NZ_LN831776.1|WP_020425558.1|7417409_7418249_+|carbohydrate-ABC-transporter-permease
MSSKTARRIGSKLLFYIPLALTLILVLVPFLWAISTSLKKETDIMSPVIHYLPQPFTFENYISVWNENNFSQYFLNSLLVSVMSVVVITLLSVMNGYAMSRFKFKGKSAFMLILLATQMMPVILFVIPLFLIFKNLGLINTPYSLVLFYIVLQVPFNTILMQGFISSTPKEIDEAGMVDGAGRFRIIFAIIAPIVLPGIVATSAFAFIGVWNEFLVAFSFITTPDRFTIPIGLKFMIGEFSVQYASLAAGSIIGLIPPVLLFMYIQRYLVEGLGGAVKG
>NZ_LN831776.1|WP_020425557.1|7418313_7419666_+|sugar-ABC-transporter-substrate-binding-protein
MTRKLRGTALVAASLLLVLSGCGSNKSSGSSSSAADGSANSSGKGEPATISFWAAAVTTERNAFFEKIIKQFEEENPDIKVDYLGVPGDLSAYEQKVNVAISAEQAPDIMNDFKADLLSRDVLEPLDTYFDSWADKDLISSELIASNRKLDTKEGKLYALPYSSQTWNLWLRPDWFKEAGLQLPDTWDQFFEDIAKLTDKSKDRYGLSIRGGAGSANTLEMLMYSYSGITDYFTPEGKSTINDPLHAEFLEKYLGAYNVYTPEDDLNKGWTELAATFQSNKAAIVVHNLGSASSHEKAFGGDYTKFEAVPFPKSVKGYREHPGLAPLGLTMSKTAKNKEAVWKFMTFYLSHDINSQYAKLYGEIPANKDAASDAWVQDIPYMKSASDLLNSADTHFADNPYYLPGYSNIQKKAESMIQKVMAKKMTGTEMLNEWAKLLEAEKQSYDQAQK
>NZ_LN831776.1|WP_020425556.1|7419693_7421262_+|glycosyl-hydrolase-43-family-protein
MNTPAATDSGHWIPDQGNGTYINPIIYADYSDPDVIRVGEDFFMTASSFTHIPGLPILHSRDLVNWRIVNHALPRLELPGYDKVQHGKGVWAPSLRYHEGQFWIFYATPDEGIFMTKTDDPFGAWEPPHLLKAAKGWIDPCPFWDEDGQAYLVHAYAHSRSGLKHILNLCRMSPDGTTLLDDGTIIVDGTVKHPTLEGPKMYKRNGYYYIFAPAGGVPTGWQAVFRSKSIYGPYEDKIVLQQGETPVNGPHQGGWVELASGESWFVHFQDKGAYGRITHLQPMEWRGDWPVMGRLAPDREAGEPVERWKKPDTAAGEVCIPQTSDDFCGAALGLQWQWQANPASNWHRLLPGGGLRLNSAPLPGDCRTLYDTPQLLMQKLAAPVFTATVKITPRFSSCAERAGLVVLGHRAFCIALSLDPAGDLWLAQYESGAADDPSRKDLGVKAAGILIQAESLYLRASFEEANGCRFSFSREGSDYIEFGSPFRLEEGQWVGAKVGLFALSLTPGEDLGYADFERFTIS
>NZ_LN831776.1|WP_020425555.1|7421624_7422857_+|MFS-transporter
MRENLDKQFSFTSLKWFNFFLYGTVVLFSSFFPLYLQEVGMNKLEIGSLMSVGALVSIIANPFWGIWTDRYQNIRRIVLLMLTGTLVLSQVVFQANTYEMIYVSILFFYFFQGPLFAESNTMILSYIDGTRHRFSSFRLWGSLGWAFTAILAGPVIEWAGVSVLSYLFAALLCAAMISLIALPRLDHSIGIAPLPFKGFRQIFYHPFFLSFIFFGILVSIPNTMNNTFVSLYITELGGSKTMIGLAVFLSSILEVAVLVLCDRYLKRSIPVLLGWLALVSALFVLRWWLMADATTPLQVAFIQILHCVTFGGFFYVGTRLTMLLVPKPYRSSGQALYTLTWSGISGIMGGVLGGWLYQYLGAQNMYQSGVFLSLIGTLGFAAMRLLASRGGYHPQDGHPEEDWNEIELNR
>NZ_LN831776.1|WP_167345686.1|7422977_7423388_+|hypothetical-protein
MPLVKRVSAPAAPAAYSKVFLPLILPLPALAAHSKVFLPLILPLPAQAAHSKVFLPLILPLPALAAHSKVFLPLILPLPAQAAYSKVFLPLILPLPAPAAHSKVFLPLILPLPAQAAHSKVFLPLICPAQRGCPVI
>NZ_LN831776.1|WP_020426049.1|7423422_7425129_-|glutamine--tRNA-ligase/YqeY-domain-fusion-protein
MENRGTPSNFIKNVITEDLSSGKVKEVVTRFPPEPNGYLHIGHAKAIWINFTLADEFGGKTHLRFDDTNPLKEDTEYVNSIQEDVKWLGYEWDELRFASDYFGEMYERAELLIQKGKAYVDDLTADQIREHRGTLTEPGVNSPYRERTIEENLDLFRRMRAGEFKDGEKVLRAKIDMSSPNINLRDPVIYRISHSHHHNTGDAWCIYPMYAFAHPLEDAIEHVTHSLCSLEFEDQRPFYDWVVAECEMPASPHQYEFGRLNLAQTVTSKRKLKLLVDEGHVDGWDDPRMPTISGLRRRGYTPEAIRSFVHETGISKSQGLVDLQMLEHFIREDLKLTVPRTMSVLRPLKVVITNYPEGQTEWFEIENNVENEAMGTRQIPFSREIYIERDDFMENPPNKYFRLFPGNEVRLKNAYFIKCTDFIKDENGEVVELHCTYDPETKSGSGFTGRKVKGTLHWVDAGQAVPAEFRLYEPLISAEEADQEAEVEGMEPAADKPEPSFLDQLNPKSIDILHGFVEPGLKDSVPQDKFQFFRHGYFNVDSRYSTPGHPVFNLIVSLKSSFQPAKQG
>NZ_LN831776.1|WP_020426050.1|7425359_7425605_+|DUF2164-domain-containing-protein
MKPIKLPKEQREIITENIRAYFEAERGESIGHLAADNLLEFFLQELGPAIYNGALGDCRTLVGQRMQSLEDDIYALEWKKR

Crispr_ID: NZ_LN831776_74

• CRISPR_ID: NZ_LN831776_74
• CRISPR_location: 7483800-7483874
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: DinG

Consensus repeat of NZ_LN831776_74

Consensus_repeat	Method
TCAAGTGGAAAAAGGATCACTAAT	CRISPRCasFinder

spacers of NZ_LN831776_74

>74.1|7483824|27|NZ_LN831776|CRISPRCasFinder
TTGCTCTAACACCATGCTGTCCGGAAG

CRISPR arrays and Neighbor proteins around NZ_LN831776_74

CRISPR arrays

The CRISPR arrays of NZ_LN831776_74

>merge|NZ_LN831776|74|7483800-7483874|CRISPRCasFinder
TCAAGTGGAAAAAGGATCACTAATTTGCTCTAACACCATGCTGTCCGGAAGTGAAGTGGAAAAAGGATCACTAAT

>NZ_LN831776|74|74|7483800-7483874|CRISPRCasFinder
TCAAGTGGAAAAAGGATCACTAAT	TTGCTCTAACACCATGCTGTCCGGAAG
TGAAGTGGAAAAAGGATCACTAAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020427720.1|7479397_7481053_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425690.1|7469045_7470014_-|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_LN831776.1|WP_039785086.1|7468277_7468958_+|CidB/LrgB-family-autolysis-modulator	unknown	unknown	gnl|CDD|377236
NZ_LN831776.1|WP_020427727.1|7489584_7491729_+|bifunctional-diguanylate-cyclase/phosphodiesterase	unknown	unknown	gnl|CDD|238923
NZ_LN831776.1|WP_020425689.1|7470067_7472377_-|hypothetical-protein	DinG	COG1199_DinG_CAS-IV-A	gnl|CDD|224120
NZ_LN831776.1|WP_020425687.1|7474599_7475031_-|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_LN831776.1|WP_020427719.1|7477156_7479166_-|EAL-domain-containing-protein	unknown	unknown	gnl|CDD|236645
NZ_LN831776.1|WP_039787347.1|7482119_7483478_+|dicarboxylate/amino-acid:cation-symporter	unknown	unknown	gnl|CDD|366058
NZ_LN831776.1|WP_020427728.1|7491852_7492176_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427726.1|7488739_7489363_+|membrane-protein	unknown	unknown	gnl|CDD|224500
NZ_LN831776.1|WP_020427721.1|7481045_7481846_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224054
NZ_LN831776.1|WP_020425686.1|7475241_7476936_+|methyl-accepting-chemotaxis-protein	unknown	unknown	gnl|CDD|223910
NZ_LN831776.1|WP_046506039.1|7494840_7496295_-|transposase	unknown	unknown	gnl|CDD|372705
NZ_LN831776.1|WP_020426246.1|7493749_7494631_+|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197666
NZ_LN831776.1|WP_020427725.1|7486252_7488619_+|EAL-domain-containing-protein	unknown	unknown	gnl|CDD|227334
NZ_LN831776.1|WP_020427724.1|7485102_7486056_-|1,4-dihydroxy-2-naphthoate-polyprenyltransferase	unknown	unknown	gnl|CDD|237373
NZ_LN831776.1|WP_020427723.1|7484007_7485009_-|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_LN831776.1|WP_046507726.1|7472634_7474521_+|LTA-synthase-family-protein	unknown	unknown	gnl|CDD|224287
NZ_LN831776.1|WP_020426245.1|7493008_7493470_-|VOC-family-protein	unknown	unknown	gnl|CDD|319941
NZ_LN831776.1|WP_020426973.1|7496756_7497233_+|sulfide-reductase	unknown	unknown	gnl|CDD|379334

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_LN831776.1|WP_020425689.1|7470067_7472377_-|hypothetical-protein	DinG	COG1199_DinG_CAS-IV-A	4.2e-87	287.6	0.9

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020425690.1|7469045_7470014_-|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	1.82049e-50
NZ_LN831776.1|WP_020425686.1|7475241_7476936_+|methyl-accepting-chemotaxis-protein	gnl|CDD|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	8.35693e-64
NZ_LN831776.1|WP_039785086.1|7468277_7468958_+|CidB/LrgB-family-autolysis-modulator	gnl|CDD|377236	pfam04172, LrgB, LrgB-like family. The two products of the lrgAB operon are potential membrane proteins, and LrgA and LrgB are both thought to control of murein hydrolase activity and penicillin tolerance.	6.72049e-81
NZ_LN831776.1|WP_020427727.1|7489584_7491729_+|bifunctional-diguanylate-cyclase/phosphodiesterase	gnl|CDD|238923	cd01948, EAL, EAL domain. This domain is found in diverse bacterial signaling proteins. It is called EAL after its conserved residues and is also known as domain of unknown function 2 (DUF2). The EAL domain has been shown to stimulate degradation of a second messenger, cyclic di-GMP, and is a good candidate for a diguanylate phosphodiesterase function. Together with the GGDEF domain, EAL might be involved in regulating cell surface adhesiveness in bacteria.	4.32733e-101
NZ_LN831776.1|WP_020425689.1|7470067_7472377_-|hypothetical-protein	gnl|CDD|224120	COG1199, DinG, Rad3-related DNA helicases [Transcription / DNA replication, recombination, and repair].	1.65572e-72
NZ_LN831776.1|WP_020425687.1|7474599_7475031_-|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	5.13451e-20
NZ_LN831776.1|WP_046506039.1|7494840_7496295_-|transposase	gnl|CDD|372705	pfam13751, DDE_Tnp_1_6, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis.	1.52639e-13
NZ_LN831776.1|WP_039787347.1|7482119_7483478_+|dicarboxylate/amino-acid:cation-symporter	gnl|CDD|366058	pfam00375, SDF, Sodium:dicarboxylate symporter family.	1.67411e-114
NZ_LN831776.1|WP_020427726.1|7488739_7489363_+|membrane-protein	gnl|CDD|224500	COG1584, COG1584, Predicted membrane protein [Function unknown].	5.41521e-22
NZ_LN831776.1|WP_020427721.1|7481045_7481846_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	8.00344e-83
NZ_LN831776.1|WP_020427719.1|7477156_7479166_-|EAL-domain-containing-protein	gnl|CDD|236645	PRK10060, PRK10060, cyclic di-GMP phosphodiesterase.	2.84765e-114
NZ_LN831776.1|WP_020426246.1|7493749_7494631_+|AraC-family-transcriptional-regulator	gnl|CDD|197666	smart00342, HTH_ARAC, helix_turn_helix, arabinose operon control protein.	1.90881e-28
NZ_LN831776.1|WP_020427725.1|7486252_7488619_+|EAL-domain-containing-protein	gnl|CDD|227334	COG5001, COG5001, Predicted signal transduction protein containing a membrane domain, an EAL and a GGDEF domain [Signal transduction mechanisms].	2.52975e-108
NZ_LN831776.1|WP_020427724.1|7485102_7486056_-|1,4-dihydroxy-2-naphthoate-polyprenyltransferase	gnl|CDD|237373	PRK13387, PRK13387, 1,4-dihydroxy-2-naphthoate octaprenyltransferase; Provisional.	9.33982e-81
NZ_LN831776.1|WP_020427723.1|7484007_7485009_-|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	6.63827e-80
NZ_LN831776.1|WP_046507726.1|7472634_7474521_+|LTA-synthase-family-protein	gnl|CDD|224287	COG1368, MdoB, Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily [Cell envelope biogenesis, outer membrane].	8.65976e-90
NZ_LN831776.1|WP_020426245.1|7493008_7493470_-|VOC-family-protein	gnl|CDD|319941	cd08353, VOC_like, uncharacterized subfamily of vicinal oxygen chelate (VOC) family. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	3.02088e-87
NZ_LN831776.1|WP_020426973.1|7496756_7497233_+|sulfide-reductase	gnl|CDD|379334	pfam13686, DrsE_2, DsrE/DsrF/DrsH-like family. DsrE is a small soluble protein involved in intracellular sulfur reduction. The family also includes YrkE proteins.	1.86413e-61

Protein sequences

>NZ_LN831776.1|WP_039787347.1|7482119_7483478_+|dicarboxylate/amino-acid:cation-symporter
MDNNLLSAIETNWQGFVISIFVFGILFLLARKRIGFGTRVLLGLGIGLIAGIFFQFFDLETEAIKTFGSIYVSLIRMLVIPLVFILVLNSISSLTNLEYLRKIGIKTFAWFLGTTGVASIIGLSVALLFNPGKGIQQAVPEGFEAREIPTFSQVILDLVPSNPVNEAATGKVVPLLIFAIFLAVAIIKVGSKKPEAVKPVRDLIESLTTVLHQVVKFVIRLTPYGVFALIAGITARYGWETLQELGSVIITSYVALIIHFVLIFGGLVLLVAKVNPLRFFRKIYPTLTVAFTTRSSYATLPVNLEVITKRLHVSPRIASFVAPLGASVNFNGCGGIWPAIVAVFTAQVFGIHLTGTDYVTLVLVSIISSIGVAGVPGPAVISTTVVLTALGLPLEGIAIVAGVEALIDMGRTAVNATGTTVTALLVANSEGEFDREAFNRGDDDEEILLNAV
>NZ_LN831776.1|WP_020427721.1|7481045_7481846_-|ABC-transporter-ATP-binding-protein
MGLTEEPVISISGLWMNYSDRMVLRGIDLEVYRGQIIGYIGPNGAGKSTTVKIMLGLVEGYTGTVRIFGRDIADGDAAYKRRIGYVPEIAELYDSLTAREYLTFIGELYGMKRTEADAKAERLMDLLNLKKAYDMRIASYSKGMKQKVLLISSMLHDPDILFLDEPLSGLDANSVMVVKEIFASLAAQGKTIFYSSHIMDVVEKISSRIILINGGDIVADGTFAQLQEQNREGSLEDIFNQLTGFDKYRDIAGEFVAVLGEGAPHE
>NZ_LN831776.1|WP_020427720.1|7479397_7481053_-|hypothetical-protein
MNDFWVLKLLDRLQGGFRRAGVDYKMLRSILQVKLTMDGRRTPTVLGTQKGSRGTEGSPLRVQWIYLLLGLMLILFVVPGSNFMLNMSVLFAVVMFMITTTLISDFSSVMLDLRDKNILFSKPVDRRTLNMAKSLHVLIYLVTLTLTFTGPSLLVALFKQGVLFFLVYAVEILLMDCFILVITALLYLLILRVFDGEKLKDIINYVQIILSVGIAAGYQLVPRLFDMADLTGSFQPAWWQYVIAPVWFAAPFEVLAGGARGVDLNVLALLSVIVPLVLLLAYIKLMPLFERSLQKLAEQGAAGKDKSRYSGLLSELFCRNKSEAMFFRFTWSMMRKERDFKLKVYPTVGLSLVLPFIFIFNRAWTSDPSMNTESKAYLFIYLCALLLLTVVQMLRYSSSYKGAWIYKTIPLPETAPVYRGMLKAALLRLMLPLFVLESAVFLWLFGAHILPGLAAVMLALPLYAVICFRVLPRALPFSEKYEAAKQRDFSVSGFVLLFILMGLAGLHYIVSLLPSGIYIYLVILAAANVWAWRAAFSHEGSRPGQIPTPGA
>NZ_LN831776.1|WP_020427719.1|7477156_7479166_-|EAL-domain-containing-protein
MDQMGIHYNLWIVLLSFALAATAAYSALNLILQVFHSAGRVRRLWLLSSACVLGSGIWAMHFVGVMASYLPFKVSYHPGIAGCSLLISMCACYLSLWVATMSPLRTGRLLLSGMILGSGISMMHYMGMYSMKLQAEIHYETLTQGLSVVVACVVSYAAVFLFHKFKDYAGFSRWKLYSAVFIGLAVTGMHYISLRASILEVDNWTGTRPLLIESDVVLLTGVSLVTLFMLAVSCGAVFLDRHVLERMAYHDPLTELPNRHGLERYFKGEFFGGHSGAVFFVDLDRFKSINDTLGHDIGDMLLQEVAGRLRGVISAKGKVFRLGGDEFLIALPVCTMEDAREEAQHILRELKKAYSIEGNELYVTASVGISMTPLHGTDRSALMKAADTALYTSKDSGKNKFSVFDQEMNRHQLRRMSLEKDLRKALARSEFMVVYQPKWDSLMNVTVGLEALLRWRHPEHGIISPAEFIPIAEETGLIVPITYWMLHDVCGQNKLWHKACVANVAVSINMSARMFEGGSLYDVVEEALVRSGLEPHFLELEITESIAMNNMEETVAQLSKLRNLGVRVSLDDFGTGFSSLGNLDEIPVNTLKIDQVFIRKSKMHSKKAIISNIIAIASNLNMEVVAEGVETPEQIELLQSLGCRVMQGFYYGRPMPVSELGQWFIENTA
>NZ_LN831776.1|WP_020425686.1|7475241_7476936_+|methyl-accepting-chemotaxis-protein
MKLATKLTWMILIVLLLVGSSIGFFGYRAAYHQVDEAAGIELVGCANITTGLIDPADITALVNGDSSKVSAIEERIGWIVAHKPIFKEAFILSLDGKILAADTSLKKRGYKAGDDFYFTEEDKAMITTMKHSAYSKVYTYQGTSLKTGYGPIYQDHDPTKPIIALMAINFDGPLIQERTLDIIVQPFIIGGSILIIAILAAYLMIRRMVSPLTKLSASVNTIARGDLTHEPLLFNSKDEIGTLARDFNDMALSLRDIITQVNDTSMLVASSSQELSASAQETNRAGEHSANVTIELAEGAGTQLKDLEGSYQAVQDMSRFITEIAGNADSAKDTAANNAQKARLGRQSLDSTTSQIGIVSESIHDLSDIIATLGSHSKEIENIVGTISSIAEETNLLALNAAIEAARAGEEGRGFAVVAGSVRKLAERSAASAGQIGELVSLIISQMDNAGETMKRSTEEMEQGKELILSAGRSFSEIETSVSDMSSQSQQISETVRELGLIAGGLVESIQKIVTVSNYTAEGAMTLSATSQEQLAAMEEVESSAGFLSSLAEKLQVLVERFKV
>NZ_LN831776.1|WP_020425687.1|7474599_7475031_-|MarR-family-transcriptional-regulator
MSQQIDPLVERLGLSMWKVQRKIASQMSLHREIGLTVPQFGLLRMIAQEQNARVIQLADKMEVKSSAVTVMLDRLELLGLSAREQDEHDRRAVIVTLTDKGEKLLEEGKNRFLLLLSEYLAILQPEELQNFADYYQMLDQQER
>NZ_LN831776.1|WP_046507726.1|7472634_7474521_+|LTA-synthase-family-protein
MQKEGEAVSSLNVKRWLIKPFVYFSILFILKSFLAWGVIFGDLLSWKTLLTEIPFVWALFALIERFASKRKLGYYMTVNLLVTAIFFAAIMYFKYYGVIVTYHAAEQVNQVTAVRNSVFSLMDPYYLLIFADIIVLGIYFFFNKKGRAYKKDNINHRGGKLSHSLLFAVSLALCLFNILPNKASMNEIKKAQEMGILNYEAYTIFAKDKPELVNASEITQDAINKLKGIDPAAVSPLQGAAKGKNLIIIQLESFQSFLLGLKVDGHEITPNLNRLMENSLYLPNFYQMVGQGNTSDAEFVVNSSFYIPPQGAATMAYVDKELPSLPRLLKDNGYQTATFHTNDVEFWNRGELYSSLGWDHYYDHKFFGDEDAFFFGPSDEALYRKTSDKLKEMEADGKPFYAQVISMSAHHPFTIPEEKYKMKLPERYEGTFVGDYIRSQNYADFAFGQFVDELKANGVWDNSLIMVYGDHMGLPIYSLDHDDKELMKEIYGHEYEYADMLNIPLIIHAEGKIGTQTLDHVGGEVDIMPTAASLLGVSMDNNIHFGQDLTSQSYNLLPQRYYLPTGSFIASSGLLIPGNSFEDNTQFTLASGGKAPAGTEDEYNRALRLRQLSDSYVTQLPDKVKDAE
>NZ_LN831776.1|WP_020425689.1|7470067_7472377_-|hypothetical-protein
MDHAEIFLSVRTLVEYAFSSGSLEPGFRSGAAMAEGTRIHQHIQKQYKEGDRKEVYLKAEIPYEGLLFIIDGRCDGLLAGEDGRLIVEEIKSIAGPLDSTMEGKEVHWAQALMYAYMIVMDQELPSIEVKLTYVLRGSDEQRSLYRTAGREELEAFASETVARYAPFAKLKVHHKARREESIRSLDFPFRDYRQGQRHFAAAVYKTTAEGVNLFAQAPTGIGKTMSTLFPAVKALGEGVVAGIFYLTAKTVTRFAAQEAVLLLLAGSLHLHAITLTAKEKACFREEGLCGKESCPYADGYYDRVNAALLDMLEHETLMTQEIIDAYARRHEVCPFEFSLDAAYACDMVICDYNYIYDPRISLKRLPEERKKKTVLLVDEAHNLVDRGREIFSASLTKAPFLNLQRQYKTVNRKLGAAAKAVNAFFIALRKSCNEDGEGHWAEYPEELPQLLEAFAAEAELELSSPSSALITPAGDGEDGLLDTYYAVQGMLRTIKTYDERYVTYAEVRRGDVFLKLFNLDPSHLLQQMAKGFRSQILFSATLSPMSYYRDMIGAAEEDYSLRVASPFHKEQWEVSVLPVSTRYRDRADSLIPLSDALRGMVARKGNYLVFFPSYAYLQNVFEVFTDKYPEITTLVQGSGMGEQAREEFLASFRPDNPQTLLGFAVLGGIFSEGVDLPGDRLNGVMIVGVGLPQVGLERNLLRGYFGSQGKNGFDYAYVYPGMCKVQQAGGRLIRSESDRGIIVLADDRFLQQPYAGLLPEEWRDYLIRT
>NZ_LN831776.1|WP_020425690.1|7469045_7470014_-|Gfo/Idh/MocA-family-oxidoreductase
MTLNIGIVGTGWFSKVHADLLAGMEDVKLQAVCGSSKQKGEDMASPYGAEGYGDITEMLDARKLDAVYICVPPQSHGAIERALIRREIPFFVEKPLGSSTEIPASLLQDIKEHGLLTSVGYHFRYQENIARLKKLLSGDKVGMIVGQWMGSMPGVAWWRDQEQSGGQFTEQTTHIVDLLRYLGGEVTEVYGMFGNRIVHEQHEGVTVADVGTVSLKLDNGIVANISNTCVLPGEVGQVGLSFYNDKGLLDWNPDRLMEVRSGDSKEYVSSGNPYAAESEAFLHAVRTGDRSRILSDYEDGYKTLKVTCAAYESAKSGLPVKL
>NZ_LN831776.1|WP_039785086.1|7468277_7468958_+|CidB/LrgB-family-autolysis-modulator
MTGLLLLVLTVAVYLLAKRIYASSSKMYASPLIITPLLIIIFLLLTGIPYESYNAGGKWLTDLLQPATIAFAIPLHKNFKVLKKHAAEIAAGVLSGTVMAVLSSMLLAKWLHLSGDLATSLVPRSVTTPIAMSISQSIGGVPSITAVFVILTGVLGTLMGPSVLRLFRIDNEIARGVSLGTAAHGTGTSKAFELSSLTGTISSIAMILTALLSIGLAPALLAVFLH
>NZ_LN831776.1|WP_020427723.1|7484007_7485009_-|Gfo/Idh/MocA-family-oxidoreductase
MTQKLRWGIMGCAQIATGSVMPAIQESETGIIQAVASRGLDKSSAVAEEFGVAQAYGSYEELLADPEVDAVYIPLPNHLHREWVIRAAEAGKHVLCEKPIALNSREAAEMVEACRRAGVHLAEAYMYRHHPRIAEVQEIIASGEIGDLRSIRGTFTYNDAGDTSNIRFKSAWGGGSLYDVGCYPLSAARLLFGAEPEAATVQAIFSPEHDNVDMMASGLVEFPGGVSLIFDCGMWAYNRQLLEVLGTEGRIELPMPFNARFDDAEFFVYSGGEVRRARATGANPYVCQADNFAAAVFGAAPVIAAEDPVLNMALIETCLASARTRQRISLKQG
>NZ_LN831776.1|WP_020427724.1|7485102_7486056_-|1,4-dihydroxy-2-naphthoate-polyprenyltransferase
MNVKSFLQFVELPTKVASMLPFLLGTLYALYRFEDFYVLRFALMFVSLLSFDMATTAINNYYDYKKAAKTHGYGYETHNAIVHYKLKESTVVAVIAVLLALAVGGGIALVAETGLLVFLLGGLSFLIGILYSFGPIPISRMPLGELFSGLFMGFVIIFISAYIHSDQTVVTLLFSEGWASLHIHISEVLYLFWFSVPAILGIAGIMLANNICDIEDDMDNRRYTLPVYIGRKNALLLFRLLYYISFADLAVLLLLGVNPVLAALLLLILIPLRRNIASFEEKQEKATTFILSVKNFMLMSVARIAVLGAAILLKVLL
>NZ_LN831776.1|WP_020427725.1|7486252_7488619_+|EAL-domain-containing-protein
MKLRKKIIIFTCVVALVTLGINYLLLHLIMLNRFEKLDEAALKHSLDDALTSYQEELLDMRTGMLNYSLRDETYRFVAASRSADRPPAADDGFIRSIFNRATFEVNHLDMMALLDKSGQPLYGGTYDTARRSMSPLTPELHTLFRLMNSRLPAFSSANDSQTGIVLLDQGPMLITLTPVAGSSTDKPVIGTAVAGRMLQQEEVTHVREDGPASIQITRATSELLAQSGGKDRWMSPVSDSMMSVHTVVNDLFGNPGVVFTVKQSRQIYESGQESVYSFRLVFFTVTILSCIGSMLFVNRSILGRMSSLIKNIRAIGSSKDLSIRIISTGRDEFSDVEHEFNRMIDSLEQAQEELQQQSMLDPLTHLPNRSLFFAKLNAAIGAAKGSNRQIALVFIDLDHFKTVNDTLGHDFGDAMLQEIAFRLTQAVGTHDVVSRLGGDEFTILLSDIPDSAAISAQLSNIQDALSMPHQIQGHLFYCTASIGISIYPQNGDDADYLVKQADLAMLHVKGTGRNNIFQYSEDLEESIRRKKVLSQQLLSAAANAEFEVHYQPILNAERLQVHKVEALLRWTSPIYGPVSPAEFIPLAETSGSIVSIGGWVLRQVCADMRRFRESGLFLTAAVNISALQLMQPGLLELLLKLLHEFELPPSSLELEITESVLVNGDSILESLQQLRAHGFRISLDDFGTGFSSLSYLRRFPVDVIKIDRSFVSEMTPHPQGDVLVKAIIELSHNLGLSVVSEGIELQEQFDMLRSLGSDELQGFYISKPVRAGEIRSFLSRKKSFLGEK
>NZ_LN831776.1|WP_020427726.1|7488739_7489363_+|membrane-protein
MSAQSPNTQSVKIVTADPSAIGLFGLAIVTLVASSQKLEITTGLSYCIPWAIFLGAFAQLFASIQDAKHNNTFGMTAFGAYAFFWFGMAASWLIKLGVFGTALAEGVDPKQLGFVFLGYLVFTLFMTLGAVEANRVLLVIFVLIDFLFLGLTMDSFGVAAEFFHKLAACSELAIGIVSLYGCGASVLNAHFGRQFLPVGDPLGIFKK
>NZ_LN831776.1|WP_020427727.1|7489584_7491729_+|bifunctional-diguanylate-cyclase/phosphodiesterase
MAFINKKPLTIILGFVVVLQLSLFYYYSLSVDREYRAEKADLSSHAVMLTSNIEERVSIVKGVSSFIQAVGFDADPNLINEYLHTAYNNNSSNVMNIMIAPDGLIRYLYPLSGNTAILGRSLLLDSALSSPGMVQETIRSGGITIDGPRTLAQGEYGMVIRQAIYHNNSFTGIVSVTLKIENIVDQLLLKDTRIFVKTEDHTFLFGTPADKEDKQLIVPVTVYNQHWLMGIPMPLHKKWEVLRSVLWIDMAILLIIAFILYIFWHQSRFNRELERVVSIRTRDLRVSKRLYEKLAHYDSLTGIPNRLYFMDEFERLLQSAEPTQTYTLFFFDLNRFKEINDTLGHSIGDQVIKTLANRLKNGKVPFKLFARTGGDEFVMVFSNLAREHIPAIAEHISGLISETLLISGAHLSLSTSIGVSLYPEHSLNKDDLLKFADMSMYQAKSQEDANYFIFDWGLREKLEQKTMIAKYLHSALEREEFVLHYQPQINAVTGKMIGMEALVRWNHPEKGLIGPGTFITAVEEAGLMIQLTDWVLREVCRQLCEWRTMGLPLLRTSINISNSWFYNRNLIENLLAVLDQYGLETSMLEFEITESTALLEEHYPLLQQMRDHGIVVSIDDFGTKYSSLNYLKHFPVNKIKIDRTFITGIGVSSIDETIIKSIVYVASQLGYDLIAEGVETQEQLDFLIKHNCPHIQGFLFFPPLPAEDIHKLAS
>NZ_LN831776.1|WP_020427728.1|7491852_7492176_+|hypothetical-protein
MNTLSTPESIATLAFALILAIIAYRVIRSMPNMAGNITAFRKRTLVWTQVALVLAVLQLNFKAGDWRFGIILGLIVLFTSSVWLAARYYDLRRPEAADPADQETGKE
>NZ_LN831776.1|WP_020426245.1|7493008_7493470_-|VOC-family-protein
MEKNKLLRMDNVGIVVESLDDAIAFFEEIGLKLEGRATVEGEWAGRVTGVGQQCVEIAMMVTPDGHSRLELSRFLTPPAISDHRTAPVNALGYLRVMFTVEDIDEMVARLTKHGAQLVGEVVQYGDSYRLCYIRGVEGLLIGLAEQLGNSGAS
>NZ_LN831776.1|WP_020426246.1|7493749_7494631_+|AraC-family-transcriptional-regulator
MNNPSSHGVYGFRFSEPDHLPLCNLFAVGHEVVTDASYHWNGMDRTDGPLLLFQYTAEGSGIFETEQETFRIGTGRAFLAEIPGNHRYYHPGDAVPWEFYFLLFRPQPLLPLWEDIKAKLGAAPAIVPGSRPIRILRDIVHEAYSGRISDPYIASSLLHQFMMELGRLSSSGPRDAAEWPTAVRDSVQFIEERYSSMIGQEQLAEQMGLSKFHLLRTFSKYVGLTPNEYLNRTRIERAIELLTATDLSIEAIASQVGYSSGSYFIKVFQKLTGQTPGSFRSGSGSLNYSRLFF
>NZ_LN831776.1|WP_046506039.1|7494840_7496295_-|transposase
MYSIRQEELFSFEDLLLMRPEDKYSQIFEHLNLAPVLHALGKKNNRGRPEELNVPAMIYSLLIAKMEGIEFVSALVRRLRFSEEFRVQCRFTGSNRIPSEASYSRLIHVLEQTGMLEDLQDTLVLSALEEEXVTGMHLALDSSIVEAWDSLFSEAASKRRAARRAKKPSDAPVAQQLQLELTEPESEPVDERPKKPVYPPGRPSAEEKERRRKEREAYEESLGPFEKTIEQMLPYTYDELLAALPRHAARCDKKNAKGRLTSYYGFKANLLVDADCQYILSGLWSSANLNDQRMAVILLKGLLLKFPRLNVKHVLGDKGYDSAAIYQLIHSLGAYPTIPMIHHKEPPKGMNSDYNPVCSQGHTYRYDSFDAKYETLKYTQPSQCKDCPLSGSGCQKVFKIRIQTDLRKHTYPARGSESFTELYKKRTAVERVFAYLKEYFGMKRTRHRGVRARVDFQLSTLAYNLSKFALDKLNQRLRNSQQVA
>NZ_LN831776.1|WP_020426973.1|7496756_7497233_+|sulfide-reductase
MGKRMNLLMFSGEYDKAMAALILANTARDIDVEVTMFFSFWGLFLVRDPDKMTLEDKTIYEKLMDVITPKGPEQLPLSRMNFSGLGKLMLEEMIEDQGAPKLIHFLKGARKKNIKFYACKLSVDIMGFKPEELLPEVEIIDAAAYLKDALESDMQLFI

Crispr_ID: NZ_LN831776_75

• CRISPR_ID: NZ_LN831776_75
• CRISPR_location: 7578894-7578968
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_75

Consensus_repeat	Method
ATTAGGGGTACTTTTTCCAACATA	CRISPRCasFinder

spacers of NZ_LN831776_75

>75.1|7578918|27|NZ_LN831776|CRISPRCasFinder
AGATACTCCATACGCTGAATGGGTCCG

CRISPR arrays and Neighbor proteins around NZ_LN831776_75

CRISPR arrays

The CRISPR arrays of NZ_LN831776_75

>merge|NZ_LN831776|75|7578894-7578968|CRISPRCasFinder
ATTAGGGGTACTTTTTCCAACATAAGATACTCCATACGCTGAATGGGTCCGATTAGTGGTACTTTTTCCAACATA

>NZ_LN831776|75|75|7578894-7578968|CRISPRCasFinder
ATTAGGGGTACTTTTTCCAACATA	AGATACTCCATACGCTGAATGGGTCCG
ATTAGTGGTACTTTTTCCAACATA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020425928.1|7581309_7582542_+|peptidase-T	unknown	unknown	gnl|CDD|235484
NZ_LN831776.1|WP_020425935.1|7586029_7586662_-|3-hexulose-6-phosphate-synthase	unknown	unknown	gnl|CDD|132172
NZ_LN831776.1|WP_020426580.1|7566067_7567045_+|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|380514
NZ_LN831776.1|WP_020425930.1|7583194_7584331_-|NADH-dependent-flavin-oxidoreductase	unknown	unknown	gnl|CDD|240086
NZ_LN831776.1|WP_020425921.1|7568709_7571718_-|beta-phosphoglucomutase	unknown	unknown	gnl|CDD|224471
NZ_LN831776.1|WP_020425922.1|7571838_7572930_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_LN831776.1|WP_020425932.1|7585053_7585374_+|cupin-domain-containing-protein	unknown	unknown	gnl|CDD|380366
NZ_LN831776.1|WP_039785285.1|7579477_7580515_+|hypothetical-protein	unknown	unknown	gnl|CDD|237057
NZ_LN831776.1|WP_020425931.1|7584395_7584770_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224647
NZ_LN831776.1|WP_020425924.1|7574318_7575746_-|carbohydrate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|224567
NZ_LN831776.1|WP_020426578.1|7561227_7564194_-|EAL-domain-containing-protein	unknown	unknown	gnl|CDD|236645
NZ_LN831776.1|WP_020425925.1|7576043_7577048_-|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_LN831776.1|WP_039785290.1|7572930_7574034_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_LN831776.1|WP_020426579.1|7564582_7565896_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_039785292.1|7577410_7578442_+|LLM-class-flavin-dependent-oxidoreductase	unknown	unknown	gnl|CDD|274646
NZ_LN831776.1|WP_052741557.1|7567545_7568010_+|DUF664-domain-containing-protein	unknown	unknown	gnl|CDD|183954
NZ_LN831776.1|WP_020425929.1|7582610_7583042_-|winged-helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|334619
NZ_LN831776.1|WP_020425927.1|7580546_7581212_+|class-D-sortase	unknown	unknown	gnl|CDD|320677
NZ_LN831776.1|WP_020425936.1|7586933_7588319_+|MATE-family-efflux-transporter	unknown	unknown	gnl|CDD|240539
NZ_LN831776.1|WP_046506068.1|7585464_7586022_-|6-phospho-3-hexuloisomerase	unknown	unknown	gnl|CDD|240138

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020425928.1|7581309_7582542_+|peptidase-T	gnl|CDD|235484	PRK05469, PRK05469, tripeptide aminopeptidase PepT.	0
NZ_LN831776.1|WP_020425935.1|7586029_7586662_-|3-hexulose-6-phosphate-synthase	gnl|CDD|132172	TIGR03128, RuMP_HxlA, 3-hexulose-6-phosphate synthase. Members of this protein family are 3-hexulose-6-phosphate synthase (HPS), or the HPS domain of a fusion protein. This enzyme is part of the ribulose monophosphate (RuMP) pathway, which in one direction removes the toxic metabolite formaldehyde by assimilation into fructose-6-phosphate. In the other direction, in species lacking a complete pentose phosphate pathway, the RuMP pathway yields ribulose-5-phosphate, necessary for nucleotide biosynthesis, at the cost of also yielding formaldehyde. These latter species tend usually have a formaldehyde-activating enzyme to attach formaldehyde to the C1 carrier tetrahydromethanopterin. In these species, the enzyme is viewed as a lyase rather than a synthase and is called D-arabino 3-hexulose 6-phosphate formaldehyde lyase. Note that there is some overlap in specificity with the Escherichia coli enzyme 3-keto-L-gulonate 6-phosphate decarboxylase.	7.80207e-85
NZ_LN831776.1|WP_020426580.1|7566067_7567045_+|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|380514	cd06291, PBP1_Qymf-like, ligand binding domain of the lacI-like transcription regulator from a novel metal-reducing bacterium Alkaliphilus Metalliredigens (strain Qymf) and its close homologs. This group includes the ligand binding domain of the lacI-like transcription regulator from a novel metal-reducing bacterium Alkaliphilus metalliredigens (strain Qymf) and its close homologs. Qymf is a strict anaerobe that could be grown in the presence of borax and its cells are straight rods that produce endospores. This group is a member of the LacI-GalR family repressors that are composed of two functional domains: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal ligand-binding domain, which is homologous to the sugar-binding domain of ABC-type transport systems that contain the type 1 periplasmic binding protein-like fold. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcription repressor undergoes a conformational change upon ligand binding which in turn changes the DNA binding affinity of the repressor.	2.57552e-117
NZ_LN831776.1|WP_020425930.1|7583194_7584331_-|NADH-dependent-flavin-oxidoreductase	gnl|CDD|240086	cd04735, OYE_like_4_FMN, Old yellow enzyme (OYE)-related FMN binding domain, group 4. Each monomer of OYE contains FMN as a non-covalently bound cofactor, uses NADPH as a reducing agent with oxygens, quinones, and alpha,beta-unsaturated aldehydes and ketones, and can act as electron acceptors in the catalytic reaction. Other members of OYE family include trimethylamine dehydrogenase, 2,4-dienoyl-CoA reductase, enoate reductase, pentaerythriol tetranitrate reductase, xenobiotic reductase, and morphinone reductase.	0
NZ_LN831776.1|WP_020425921.1|7568709_7571718_-|beta-phosphoglucomutase	gnl|CDD|224471	COG1554, ATH1, Trehalose and maltose hydrolases (possible phosphorylases) [Carbohydrate transport and metabolism].	0
NZ_LN831776.1|WP_020425922.1|7571838_7572930_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	3.55649e-73
NZ_LN831776.1|WP_020425932.1|7585053_7585374_+|cupin-domain-containing-protein	gnl|CDD|380366	cd02238, cupin_KdgF, pectin degradation protein KdgF and related proteins, cupin domain. This family includes bacterial and archaeal pectin degradation protein KdgF that catalyzes the linearization of unsaturated uronates from both pectin and alginate, which are polysaccharides found in the cell walls of plants and brown algae, respectively, and represent an important source of carbon. These polysaccharides, mostly consisting of chains of uronates, can be metabolized by bacteria through a pathway of enzymatic steps to the key metabolite 2-keto-3-deoxygluconate (KDG). Pectin degradation is used by many plant-pathogenic bacteria during infection, and also, pectin and alginate can both represent abundant sources of carbohydrate for the production of biofuels. These proteins belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold.	1.31445e-44
NZ_LN831776.1|WP_039785285.1|7579477_7580515_+|hypothetical-protein	gnl|CDD|237057	PRK12323, PRK12323, DNA polymerase III subunit gamma/tau.	3.05533e-09
NZ_LN831776.1|WP_020425931.1|7584395_7584770_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	1.42373e-43
NZ_LN831776.1|WP_020425924.1|7574318_7575746_-|carbohydrate-ABC-transporter-substrate-binding-protein	gnl|CDD|224567	COG1653, UgpB, ABC-type sugar transport system, periplasmic component [Carbohydrate transport and metabolism].	4.60265e-32
NZ_LN831776.1|WP_020426578.1|7561227_7564194_-|EAL-domain-containing-protein	gnl|CDD|236645	PRK10060, PRK10060, cyclic di-GMP phosphodiesterase.	1.37977e-106
NZ_LN831776.1|WP_020425925.1|7576043_7577048_-|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	1.98096e-118
NZ_LN831776.1|WP_039785290.1|7572930_7574034_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	4.77569e-62
NZ_LN831776.1|WP_020425927.1|7580546_7581212_+|class-D-sortase	gnl|CDD|320677	cd05828, Sortase_D_1, Sortase domain found in subfamily 1 of the class D family of sortases. Class D sortases are cysteine transpeptidases distributed in Gram-positive bacteria (mainly present in Firmicutes). The prototypical subfamily 1 of class D sortase from Bacillus anthracis (named Ba-SrtC) covalently attaches proteins bearing a noncanonical LPNTA sorting signal, such as the BasH and BasI proteins, to the peptidoglycan of the cell wall that facilitate sporulation. BasH is exclusively anchored to the forespore cell wall envelope, while BasI is attached to the diaminopimelic acid moiety of the peptidoglycan of predivisional cells. Ba-SrtC lacks the N-terminal signal peptide and membrane anchor. The family also includes many class D sortase homologs from Gram-negative bacteria, but the functions of these enzymes are unknown.	9.93967e-56
NZ_LN831776.1|WP_039785292.1|7577410_7578442_+|LLM-class-flavin-dependent-oxidoreductase	gnl|CDD|274646	TIGR03558, oxido_grp_1, luciferase family oxidoreductase, group 1. The Pfam domain family pfam00296 is named for luciferase-like monooxygenases, but the family also contains several coenzyme F420-dependent enzymes. This protein family represents a well-resolved clade within family pfam00296 and shows no restriction to coenzyme F420-positive species, unlike some other clades within pfam00296. [Unknown function, Enzymes of unknown specificity].	0
NZ_LN831776.1|WP_052741557.1|7567545_7568010_+|DUF664-domain-containing-protein	gnl|CDD|183954	PRK13291, PRK13291, putative metal-dependent hydrolase.	1.47223e-09
NZ_LN831776.1|WP_020425929.1|7582610_7583042_-|winged-helix-turn-helix-transcriptional-regulator	gnl|CDD|334619	pfam01638, HxlR, HxlR-like helix-turn-helix. HxlR, a member of this family, is a DNA-binding protein that acts as a positive regulator of the formaldehyde-inducible hxlAB operon in Bacillus subtilis.	1.5246e-41
NZ_LN831776.1|WP_020425936.1|7586933_7588319_+|MATE-family-efflux-transporter	gnl|CDD|240539	cd13134, MATE_like_8, Uncharacterized subfamily of the multidrug and toxic compound extrusion (MATE) proteins. The integral membrane proteins from the MATE family are involved in exporting metabolites across the cell membrane and are responsible for multidrug resistance (MDR) in many bacteria and animals. A number of family members are involved in the synthesis of peptidoglycan components in bacteria.	2.00995e-176
NZ_LN831776.1|WP_046506068.1|7585464_7586022_-|6-phospho-3-hexuloisomerase	gnl|CDD|240138	cd05005, SIS_PHI, Hexulose-6-phosphate isomerase (PHI). PHI is a member of the SIS (Sugar ISomerase domain) superfamily. In the ribulose monophosphate pathway of formaldehyde fixation, hexulose-6-phosphate synthase catalyzes the condensation of ribulose-5-phosphate with formadelhyde to become hexulose-6-phosphate, which is then isomerized to fructose-6-phosphate by PHI.	1.55628e-77

Protein sequences

>NZ_LN831776.1|WP_039785292.1|7577410_7578442_+|LLM-class-flavin-dependent-oxidoreductase
MQEGLLVKKLQDIPFSVLDLAPIVEGGTAADSFHNTLDLARHAEAWGYHRYWLAEHHNMPGIASSATSLVIGHVAAGTKSIRVGSGGIMLSNHAPLMIAEQFGTLESLYPGRIDLGLGRAPGSDQAAARAMRRGLGQDGSEFPEQLSELRAYFDPDGAGSRPLGVRAVPGEGLNVPIWLLGSSGFSAQLAGQLGLPFAFASHFAPDYLLPALHLYRTSFKPSAVLDKPHVMVGLGITAAETTEQARWLATSQQQQFLNIIRGRTGKLQPPVDSMEGLWSPQEKAMLLSKQLYSIAGDQAAIKERLLQIVEETQADEFIVASQIYDHSARLHSYELVADLVKGS
>NZ_LN831776.1|WP_020425925.1|7576043_7577048_-|LacI-family-DNA-binding-transcriptional-regulator
MKPTIRDVAKMAEVSISTVSRVMNAPQTVVESKRSRVIEAIEKLKYQPNAFARGLIYKKSNTLGLLIPDIENLYFAGVIRGMQDACIKLGYSLMICNTDRDKERMLSYIDTFHEKQVDGIVYASDVLYPECYEKLTGCRIPFVLVSSHSEEFDVPSVEVDDERAAYDAVKFLIELGHTQIGMIGFNHDNSVSGPPRYEGFVRALNEAGLEHSIEQVRYANHRFEHAYQAAHELFTDYPQVTALFCVADEFAMGAISYLKDRNILVPGQVSVIGFDNLRMSGMYIPKLTTIAQPIYQLGYRAAEKLHELLTTGKVEVPTEKMEHKLIVRESSRER
>NZ_LN831776.1|WP_020425924.1|7574318_7575746_-|carbohydrate-ABC-transporter-substrate-binding-protein
MKKATGRKLSLAMVLCLSFTMMLSGCGGNNNTNNAAKTDPPAATEAPAASNSQASPEASEAAAAGSPLDLAMKGEYKGTKVTMFGPFVDADQVKFESSIKEFEAKTGIDIQYEGSKEFEATINIRVDGGNAPDIADFPQPGLLASIAKTGKVVDLTGVLDQEKLKANYNKSWLDMSTMDGKDGKIMAGIWNRSNVKSLVWYPKKQFDAAGYTVPETWDDMMALTEQIAKDGDPAWTIGIESGAATGWAATDWIENIMLRTTTPENYDKWVKGELPFTSPEVKNAVEVMSKIWLNKDYVYGGTKSIVTTAFGDAPKPMFENPPKAWFNLMGNFITSFFPETAKVDQDYDWFYLPPIDPQYGKPVLVAGDIYAMFNDRPEVRAVMEFFTTGESIKTWVQSGGVIAPMNDASLDWYTSESDRRMAKLVQDASTLRFDGSDLMPGKVGAGTFWKGMTDYVSGTATLDKALEQIQSGWNN
>NZ_LN831776.1|WP_039785290.1|7572930_7574034_-|sugar-ABC-transporter-permease
MKPKSSDPGAQVKQSISIKAVLLSLGVLLANIVINGLIFMFFRDSTLNPLLTAVLAVLWGVLGVYLIYYTLTWAVEQYPDHIRRKVLPYIFIGPAVIILGWLLVLPALRTLYLSFFNASSEKFVGLSNYAAIFSDHLMATALRNNLLWVFIGTLACVSFGLLIAILADRSSYEKIAKSIIFMPMAISFVAAGVIWKFVYYYQPGDEQIGLLNAIVTYFGGEPQAWTSMLQPWNNFFLIVILIWMQTGFAMVIFSAAIKGVPDDILEAARVDGAGEVKIFFGIMIPFISATILTVTTTIIVFTLKIFDVVMVMTGGQYDTEVVATQFYRQFFMYRNFGYGSTLAIVLLIAVLPVILINLRQFRKQGGF
>NZ_LN831776.1|WP_020425922.1|7571838_7572930_-|carbohydrate-ABC-transporter-permease
MAGKKKRKGSKTIVNLVLGVICFIWLLPTLGLFISSFRPAADILQTGWWKVFPHQEWTQGETLQLSKDTDLRQPIEVNGQTYTDDQLKAGVKVDDSRLMWENRRARTINVQEQGWKTIPDFTMDNYNNVLSGKEYKLTEADGSETVQKGTGLSQAFWNTLTIAVPATVIPVLIASFAAYAFAWLRFPGRKTLFVIIIAMLVIPIQVALIPVLKDYTSLGLNGSYLGIWLAHTAFGLPLVTYFMYNFISQLPKDLFESAFIDGASHFTIFSRLILPLSVPALASIGIFQFLWVWNDYLVSLIFIGNQPSVQVMSMKIADLVGSRGNDWHLLTSAAFISMLMPLAIFFLLQKYFVRGLMGGSVKG
>NZ_LN831776.1|WP_020425921.1|7568709_7571718_-|beta-phosphoglucomutase
MKMKPYEHPAALYPYREWSLDEDYYQDEYNQRSESVFALGNGYIGMRGNFEEGYHGLAGTAVAGNYLNGFFDSEPIVYPEGAYGYPGRNQAMLNVTDARIIKLSVEGHAFHLNSGTVHRYARRLDMKSGILHREVEWESPAGHRVLLQIRRMVALQHKHLAAIEYRVTALNFDGTLKLDSAMDGEIARPEASDDPRLGAGRTEPSLLLEETGDEGAGGFLWMKQRTRHTGFALVTAMGHELQAESGREISRERTGERVSVCYAAAVRSGESVTLSKYITYHTSKDYDEAELLSRSASVLDMAGKCGFAGLAAEQQAYLDTFWSHTDVEITGDPALQQGIRFNAFQLLQSAGRDGVTNIGAKGLTGEGYEGHYFWDTEMYMLPFFTYTQPAVSRALLEFRYATLGKARERAAVMSQKGALYPWRTIDGAENSAYFPAGTAQAHINADIAYGIKQYVQATGDVEFLAAKGAEMLFETSRFWADLGHYNPARGGAFCIDAVTGPDEYTAIVNNNAYTNLMVRDQLLYAYETEDWLRREYPGDYARLQHEMGLSAEEADGWLEAAEKMFIPFDKALGIYAQDDTFLSKQKWDFGRTPADKYPLLLHYHPLVIYRHQVLKQADLVMALFLLGDQFSLADKIRNYQYYEPLTTHDSSLSPCIHSIVSAEIGDLAGAYAYFDRTVRMDLDDINRNAKDGLHMAAMAGSWMSIVNGFGGMRQYNGQLCFSPALPEQWESYRFKITYSGQLLDIYVGREAAVYTLLEGEGLEIRHKEQTLRLSPQEPIRVPLTKRLEAVIFDLDGVITDTAEYHYLAWQALADELGVPFSREKNERLKGVSRLESLDIVLEDSGLSLPEAAKLRLAEQKNDHYREMIGRITPADLLPGVPELLDSLRERGILVGLASASLNAPVILERLGAAHWFQAIADPAGLRKGKPDPEIFLQAAGLLGVTPGNCIGVEDAAAGIAAIKAAGMKAVGIGSPAQLGDADLLLPRAAELSVEKLLELIRQ
>NZ_LN831776.1|WP_052741557.1|7567545_7568010_+|DUF664-domain-containing-protein
MVQTTISGLQSLLKEVPAAFISISPEEVAAPRPGGKWSKLQLLGHLCDSAVNNLSRFIKVQYEPQPLRLALYDQNEWMAAQQHGSATQEEVLALWVSLNQAILRVISGLTSDQLRLLFLKESGETVTLQWLIEDYLEHMKHHLGQIFPDDSRTI
>NZ_LN831776.1|WP_020426580.1|7566067_7567045_+|LacI-family-DNA-binding-transcriptional-regulator
MPTIKDVALKAGVSATTVSRVLNNRGYLSEALKQRVYSAMEELNYRPNELARSLSRSRSNIIGLIIPLVSLPFFSELTSYIEEHAYLNGYKLLLCNSQQDKIKELEYIDMLRSSRVDGIIMGSHTLEVEAYRQMNLPLVTFDRQISPGIPFVCSDNYTGGQLATTLLIEKGCRKLAHIGGHPELNLLSNLRYEAFVETARLAGIWHTSLHTDNNSFDVLAYERLLEQLFREHSGIDGIFAGSDLIAAFALKACRERGRRVPADVRIVGYDGTALCSLNHPSITTIRQPMEEMGRLAVELILKQVEGMSVPSANILPVKLQEGSTT
>NZ_LN831776.1|WP_020426579.1|7564582_7565896_+|hypothetical-protein
MKRKITLFIAMLITLFSGQNAFGSASNQAIGAIMGGGNFTNGSTTQMNCFQALNTIGIGMTRVNLYPQYYYADNAPTPERLDSMMLQSYQHGITPMILFEYYGSYEKNGQLLGNYDKWYSIGQAFADRFRPNGKWAQANGIQNWGVTIYTALNEPDVENLISKTDYHNALEGLADGVHSVDKSLKVNPGGFAKANSNSDYTLGGYGPAIADLYNSGKLDGIDLHTYYDIQYAPMKGTYKYSAQSNFDSVKRASGITADVNFYATEFNFKKRLITEEEAAKGFFTAIWDNLGVVKNDGKTPATQFAFPWSLFNSATTDTFYGLSSSPDSWVPVTRGKTLENVIEKTKGMSFVSLDPKKTGEYVLNGSRKKLWVWQNLDYWTNHPGTSYTINGLPNGTYKLEVIGWNGVRQTIAISGKTSYTINNLAVGETYMFLAYTK
>NZ_LN831776.1|WP_020426578.1|7561227_7564194_-|EAL-domain-containing-protein
MVAGRFYLKVFQSWRMPLLLVAMLSAFLFPALTVKAEGQPPQNVLVLHSYQKGFAWTDEQSGGIEERLKGAENAPVIYTEYMDWKRYPSQENLRQLYQTIKLKYHNIHVDAIITTDDAALSFALKYRQEILDDAPIIFSGVNELGVENIPDKRKITGVIEKIDPTRTIQMALQINPSIRKVYVVFDNSESGLSTGRLVMDQIASLNQGLELIPLNRLSSEQIIHTVSGLSSDSIVLMTTYYSDSTGRIIEFERFASELGRSSSVPVYHLYDFALNHGAFGGSLISGKIQGQTSAELALRILQGERADELPIVTDSTMRIVYDYNELRHFGIPLNKLPEGSEIINKPFSFYETYRTLVLGISAAFAVLVVFILLLLFYVQLVKRMRSHLEKSNERFSLAAFGSDAVIWDVDMSTMIYYFSDSWYELLGYERGEVNESHGGWREIVHPEDAEQEDRLRTQHLEGRSSYYYAEYRMRSKSGEYIWFQARGKVLRSAGGGYIRFAGSMVDVTDRKGYESKLQISYQELESTYEELTALQDELMEQYNKVVENQELLQASEEKYRLLAYNDVLSGLPNRLSLSEELTDFIEKHPGGQAALFFLDIDNFKYINDTMGHTFGDELLVKAGERLLELSDGRCRHFRFGGDEFVILIKEVDRYAEVIYYAESLVQGFSAPFELDASSVHISISIGIASYPENGTDAGELLKNADIAMYKAKEAGKGTYVVYGEEMQQHFDERMIVEHHLRNAIANNELSLQYQPLVDTGTGRIWGFEALIRWNNPVLGIVSPLSFITIAEDCRLIVPIGEWVLRKACRFMKELQAQGYEGYHISVNISVVQLMLDDFTDMVLAVLEDTGLAPEYLELEITESIFMESFEAVSSKLEPLKQRGIGIALDDFGTGYSSLSYLKQLPITTLKIDKSFIDSIDTPNNMSLASSIVTIGHDMGLNVTAEGVETQEQLAFLEQTSCDKIQGYFISRPIPQKEVAGWISGRPAG
>NZ_LN831776.1|WP_039785285.1|7579477_7580515_+|hypothetical-protein
MKKKYHKAILGLYILIVLAGVVWHAGGVSAEDTIKLTVNSHTTSMAKMANMQPGDVTTSDYTVINEGKEPFNYYVDFKFMSGDRELYNILQMTLQKEGVILYSGVMSEAEGRVAVGRLAGGGQEAIQMDVTFPYEAGNEYQATTASVAFVFSASGEPGPSAEPSATPSASVTPNPSAEPSATPSASVTPNPSAEPSATPSASVTPNPSADPSDAPNPPSGPTASPAGSSVPGTIATPSASPSAAASPGPDEAAVTDPPVPLGGHNSSRGNAPSASPGPGSTGAGTEAAPSPDYETPLNDNELPLGGPDGGDKLPDTAEPWYNLVLLSLAVAVVSVIILRRLNSKK
>NZ_LN831776.1|WP_020425927.1|7580546_7581212_+|class-D-sortase
MKKRSGLVIAVKLVFVLSLCVLLYSAFQILKAPVEARQALQEWEKKREEAPNLYHTEEEAPLPDGMATPLEGTPPSKPAYTIGDIIGEIYLPRLDKRIAIVEGTERLQLKKGAGHDPGSAPIGAAGNSVLAGHRDTVFRGLGALQKNDLIEVETAEGRFTYSVTGSTIVDGDARGVIKQSDEAVLTLITCYPFTYVGSAPDRYLLSAVLLRKEPVSLSLQP
>NZ_LN831776.1|WP_020425928.1|7581309_7582542_+|peptidase-T
MKEKLIERFISYAQMDTQSNDDNEACPSTPGQMELARKLAAELQELGLVEVTVDEHAYVMATLPANTDKEVPVIGFLAHLDTATDFTGAGVKPQLVENYDGKDIVLNKELDIVLSTESFPELAGYKGHTLITTDGTTLLGADNKAGIAEIMTAMAHLLEHPEIKHGKIRVAFTPDEEIGRGPHKFDVARFGASHAYTVDGGPLGELEYESFNAAGVKISFKGVNVHPGTAKGKMIHSAKIAMAFHLRLPSGEAPEFTEGYEGFYHLISMQGTAEQSKLQYIIRDFDREAFENRKAYIAAIVEEFQSTYGAENIVLEMKDQYYNMREKIEPVRHIVDIAQEAMENLGITPVIRPIRGGTDGSQLSYMGLPTPNIFTGGENFHGKFEYASVDVMLKAVQVIVEIAKLTEQKA
>NZ_LN831776.1|WP_020425929.1|7582610_7583042_-|winged-helix-turn-helix-transcriptional-regulator
MNVQRSRGAANSKDSQESLQSTLDLIGGKWKGVLLYHLISGTKRFNEIRRLCPEITQRMLTLQLRDLERSGLVHRKVYPQAPRKVEYSLTEWGRGLEAAILSIKSWGEAYREEFGKAHPQLPGYQAPSPAADPACKTDTNIPG
>NZ_LN831776.1|WP_020425930.1|7583194_7584331_-|NADH-dependent-flavin-oxidoreductase
MSTTDYSPLLEPFQFASSISLKNRVVMAPMTNLSSNEDGTVSGPEIDYYVRRSKGAGMVITACVYVSRGGKGFAGEFGADRDELIPSLRRLAEAIKGEGAKAVLQIFHGGRQCPPEQLLDGQPVGASNVPSELPGGGHGPVPRALADDEIEGIIADFGAAARRAIEAGFDGVEIHGANGYLLQQFFSPHSNTRSDRWGGDLQKRLAFPLAVLRAVKSAVKKHASSPFLVGYRFSPEEPETPGITMSETFALIDALKEEGLDYLHVSQMDLWSRPHRGTGDSRPRIEQIVDRAGSGLPVIGVGSLYSADDALKSLSSGISLVALGRPLLIEPDWVQKVAEGRADEIDTELDPAAQDALVIPDPLWRALIHTPGWLPVKS
>NZ_LN831776.1|WP_020425931.1|7584395_7584770_-|helix-turn-helix-transcriptional-regulator
MATEIKDRINLKEINCEKELTLAVIGGKWKLIILWHLGLEGTKRFSELKKLIPHITQKMLTNQLRELEEDQLVFRQVYAEVPPRVEYSLTEYGQSLLPVLRMMYDWGKNYGENVIWKDIPPGDR
>NZ_LN831776.1|WP_020425932.1|7585053_7585374_+|cupin-domain-containing-protein
MGKLGVWEPAEPGVKRCILNAAGSLMMMEVHFEEGAEGYEHSHPHEQMSYCLRGSFEFRIDGKKHKVSAGQSIAIPPNAKHGVTALEADSALLDAFTPIREDLLKR
>NZ_LN831776.1|WP_046506068.1|7585464_7586022_-|6-phospho-3-hexuloisomerase
MNTFSYAQEIVNELQRSVAQLGAAEAEQMAELLLRSGRVFVAGAGRSGLMGRAFAMRLMHAGKDAYVVGETVTPGIGPGDVLVLGTGSGETASLLSMAVKARAVGAAVVAVTLSPESSIGLLADHVVKLPGAPKEQADGGRITIQPMASLFEQTLLLFYDAVILRMMEETGQTSTRMFGNHANLE
>NZ_LN831776.1|WP_020425935.1|7586029_7586662_-|3-hexulose-6-phosphate-synthase
MKLQLALDLVNIDGAKEIVSEVAGFIDIVEIGTPIVINEGLHAVKAIKEAFPALTVLADLKIMDAGGYEVMKAAEAGADIVTVLGVSDDSTIKGAVEEAKKSGREILVDLINVKDIAARAAEVDALGVDYVCVHSGYDHQAEGKNSFADLQAIKSVVKQAKTAIAGGIKLNTLPEVIAAGPDLVIVGGGITGESDQKAAAAEMKRLVSQA
>NZ_LN831776.1|WP_020425936.1|7586933_7588319_+|MATE-family-efflux-transporter
MNQTKHQEFNLVKLTWPIFLELFLFMLMGSVDTFMISSVSDDAVSGVGAANQIISIAILVLSVIGNGAAIVVSQYLGSRKPKEAAEVTGNAVTLNLAVGIIFSTAILVFGEALLRALNVTGDILIHAKVYIHIVGGGIFLQALINALATTIRTYGFTKQTMMVSLLMNLIHVAGNYLLIFGHFGLPALGVQGAAISTVASRLICLVIFFLLLYRIMEVRVKLAYYIHLSKKYVLQILKIGIPSAFESVIYQSCQLIFTLYITYLGAEAMATRQYALNISNYIYLFSVAVAMGTSIIVGHLVGARRPEEAYKRVFKSVKWALLVTVIIDVAVIFFRVPLMGLFTDNLEIIALGAQVILLSIFLETGRTCNLVIINSLRASGDAKFPVYMGFISMVCISLPLGYVLVFQLHLGLAGVWLATAADEWLRAVIMFFRWKSRAWVKHRLIEHETAEPAAPTAASSH

Crispr_ID: NZ_LN831776_76

• CRISPR_ID: NZ_LN831776_76
• CRISPR_location: 7622352-7622425
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_76

Consensus_repeat	Method
ATTAAGTTCCCTTTTTCCACTTA	CRISPRCasFinder

spacers of NZ_LN831776_76

>76.1|7622375|28|NZ_LN831776|CRISPRCasFinder
AATCTCTCAATTGTTGATTTTTAGGAGG

CRISPR arrays and Neighbor proteins around NZ_LN831776_76

CRISPR arrays

The CRISPR arrays of NZ_LN831776_76

>merge|NZ_LN831776|76|7622352-7622425|CRISPRCasFinder
ATTAAGTTCCCTTTTTCCACTTAAATCTCTCAATTGTTGATTTTTAGGAGGAATAAGTTCCCTTTTTCCACTTA

>NZ_LN831776|76|76|7622352-7622425|CRISPRCasFinder
ATTAAGTTCCCTTTTTCCACTTA	AATCTCTCAATTGTTGATTTTTAGGAGG
AATAAGTTCCCTTTTTCCACTTA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020427420.1|7614420_7615770_-|MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_LN831776.1|WP_085981544.1|7624252_7624912_-|S-layer-protein	unknown	unknown	gnl|CDD|306825
NZ_LN831776.1|WP_039786996.1|7614175_7614382_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427430.1|7626890_7627733_+|aldo/keto-reductase	unknown	unknown	gnl|CDD|381383
NZ_LN831776.1|WP_020427422.1|7617004_7620085_-|response-regulator	unknown	unknown	gnl|CDD|225814
NZ_LN831776.1|WP_081487140.1|7623764_7623947_+|response-regulator	unknown	unknown	gnl|CDD|381147
NZ_LN831776.1|WP_020425574.1|7628455_7629733_-|IS91-family-transposase	unknown	unknown	gnl|CDD|377437
NZ_LN831776.1|WP_020425834.1|7631713_7632052_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224647
NZ_LN831776.1|WP_020427417.1|7612209_7613427_-|glutathionylspermidine-synthase-family-protein	unknown	unknown	gnl|CDD|367631
NZ_LN831776.1|WP_020427416.1|7611560_7612223_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427429.1|7625520_7626726_+|MFS-transporter	unknown	unknown	gnl|CDD|225371
NZ_LN831776.1|WP_020427426.1|7623886_7624138_+|ATP-binding-protein	unknown	unknown	gnl|CDD|340399
NZ_LN831776.1|WP_020427421.1|7615849_7616974_-|response-regulator	unknown	unknown	gnl|CDD|226456
NZ_LN831776.1|WP_020425833.1|7630607_7631537_-|AEC-family-transporter	unknown	unknown	gnl|CDD|223751
NZ_LN831776.1|WP_020427424.1|7621515_7622130_-|xanthine-phosphoribosyltransferase	unknown	unknown	gnl|CDD|181705
NZ_LN831776.1|WP_020427425.1|7623055_7623610_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_085981542.1|7625021_7625384_-|winged-helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|334619
NZ_LN831776.1|WP_046507758.1|7613423_7614110_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020427423.1|7620217_7621522_-|purine-permease	unknown	unknown	gnl|CDD|274468
NZ_LN831776.1|WP_020427415.1|7611171_7611564_-|DUF350-domain-containing-protein	unknown	unknown	gnl|CDD|226289

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020427420.1|7614420_7615770_-|MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	2.48729e-35
NZ_LN831776.1|WP_020427430.1|7626890_7627733_+|aldo/keto-reductase	gnl|CDD|381383	cd19157, AKR_AKR5G1-3, AKR5G family of aldo-keto reductase (AKR). Bacillus subtilis glyoxal reductase (GR), uncharacterized oxidoreductase YtbE, and Bacillus aryabhattai aldo-keto reductase are founding members of aldo-keto reductase family 5 member G1-3 (AKR5G1-3), respectively. GR (YvgN, EC 1.1.1.283), also called methylglyoxal reductase, reduces glyoxal and methylglyoxal (2-oxopropanal). It is not involved in vitamin B6 biosynthesis.	0
NZ_LN831776.1|WP_020427422.1|7617004_7620085_-|response-regulator	gnl|CDD|225814	COG3275, LytS, Putative regulator of cell autolysis [Signal transduction mechanisms].	1.71882e-51
NZ_LN831776.1|WP_081487140.1|7623764_7623947_+|response-regulator	gnl|CDD|381147	cd19920, REC_PA4781-like, phosphoacceptor receiver (REC) domain of cyclic di-GMP phosphodiesterase PA4781 and similar domains. Pseudomonas aeruginosa cyclic di-GMP phosphodiesterase PA4781 contains an N-terminal REC domain and a C-terminal catalytic HD-GYP domain, characteristics of RpfG family response regulators. PA4781 is involved in cyclic di-3',5'-GMP (c-di-GMP) hydrolysis/degradation in a two-step reaction via the linear intermediate pGpG to produce GMP. Its unphosphorylated REC domain prevents accessibility of c-di-GMP to the active site. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.25805e-14
NZ_LN831776.1|WP_020425574.1|7628455_7629733_-|IS91-family-transposase	gnl|CDD|377437	pfam04986, Y2_Tnp, Putative transposase. Transposases are needed for efficient transposition of the insertion sequence or transposon DNA. This family includes transposases IS1294 and IS801. This is a rolling-circle transposase.	1.83895e-38
NZ_LN831776.1|WP_020425834.1|7631713_7632052_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	5.38779e-37
NZ_LN831776.1|WP_020427417.1|7612209_7613427_-|glutathionylspermidine-synthase-family-protein	gnl|CDD|367631	pfam03738, GSP_synth, Glutathionylspermidine synthase preATP-grasp. This region contains the Glutathionylspermidine synthase enzymatic activity EC:6.3.1.8. This is the C-terminal region in bi-enzymes. Glutathionylspermidine (GSP) synthetases of Trypanosomatidae and Escherichia coli couple hydrolysis of ATP (to ADP and Pi) with formation of an amide bond between spermidine and the glycine carboxylate of glutathione (gamma-Glu-Cys-Gly). In the pathogenic trypanosomatids, this reaction is the penultimate step in the biosynthesis of the antioxidant metabolite, trypanothione (N1,N8-bis-(glutathionyl)spermidine), and is a target for drug design. This region, the pre-ATP grasp region, probably carries the substrate-binding site.	7.97539e-62
NZ_LN831776.1|WP_020427429.1|7625520_7626726_+|MFS-transporter	gnl|CDD|225371	COG2814, AraJ, Arabinose efflux permease [Carbohydrate transport and metabolism].	3.63307e-102
NZ_LN831776.1|WP_020427426.1|7623886_7624138_+|ATP-binding-protein	gnl|CDD|340399	cd16922, HATPase_EvgS-ArcB-TorS-like, Histidine kinase-like ATPase domain of two-component sensor histidine kinases, many are hybrid sensor histidine kinases, similar to Escherichia coli EvgS, ArcB, TorS, BarA, RcsC. This family contains the histidine kinase-like ATPase (HATPase) domains of various two-component hybrid sensor histidine kinases (HKs), including the following Escherichia coli HKs: EvgS, a HK of the EvgS-EvgA two-component system (TCS) that confers acid resistance; ArcB, a HK of the ArcB-ArcA TCS that modulates the expression of numerous genes in response to respiratory growth conditions; TorS, a HK of the TorS-TorR TCS which is involved in the anaerobic utilization of trimethylamine-N-oxide; BarA, a HK of the BarA-UvrY TCS involved in the regulation of carbon metabolism; and RcsC, a HK of the RcsB-RcsC TCS which regulates the expression of the capsule operon and of the cell division gene ftsZ. Proteins having this HATPase domain also contain a histidine kinase dimerization and phosphoacceptor domain (HisKA), with most having accessory sensor domain(s) such as GAF, PAS and CHASE; many are hybrid sensor histidine kinases as they also contain a REC signal receiver domain.	1.2557e-34
NZ_LN831776.1|WP_020427421.1|7615849_7616974_-|response-regulator	gnl|CDD|226456	COG3947, COG3947, Response regulator containing CheY-like receiver and SARP domains [Signal transduction mechanisms].	4.24162e-73
NZ_LN831776.1|WP_020425833.1|7630607_7631537_-|AEC-family-transporter	gnl|CDD|223751	COG0679, COG0679, Predicted permeases [General function prediction only].	3.60877e-34
NZ_LN831776.1|WP_020427424.1|7621515_7622130_-|xanthine-phosphoribosyltransferase	gnl|CDD|181705	PRK09219, PRK09219, xanthine phosphoribosyltransferase; Validated.	1.24864e-96
NZ_LN831776.1|WP_085981544.1|7624252_7624912_-|S-layer-protein	gnl|CDD|306825	pfam00395, SLH, S-layer homology domain.	0.000123195
NZ_LN831776.1|WP_085981542.1|7625021_7625384_-|winged-helix-turn-helix-transcriptional-regulator	gnl|CDD|334619	pfam01638, HxlR, HxlR-like helix-turn-helix. HxlR, a member of this family, is a DNA-binding protein that acts as a positive regulator of the formaldehyde-inducible hxlAB operon in Bacillus subtilis.	2.02228e-48
NZ_LN831776.1|WP_020427423.1|7620217_7621522_-|purine-permease	gnl|CDD|274468	TIGR03173, pbuX, xanthine permease. All the seed members of this model are observed adjacent to genes for either xanthine phosphoribosyltransferase (for the conversion of xanthine to guanine, GenProp0696) or genes for the conversion of xanthine to urate and its concomitant catabolism (GenProp0640, GenProp0688, GenProp0686 and GenProp0687). A number of sequences scoring higher than trusted to this model are found in different genomic contexts, and the possibility exist that these transport related compounds in addition to or instead of xanthine itself. The outgroup to this family are sequences which are characterized as uracil permeases or are adjacent to established uracil phosphoribosyltransferases.	1.18101e-172
NZ_LN831776.1|WP_020427415.1|7611171_7611564_-|DUF350-domain-containing-protein	gnl|CDD|226289	COG3766, COG3766, Predicted membrane protein [Function unknown].	1.49058e-13

Protein sequences

>NZ_LN831776.1|WP_020427424.1|7621515_7622130_-|xanthine-phosphoribosyltransferase
MKILEERIREEGLILSDTVLKVDSFLNHQVDTQLALQIGEEFGRIFGHLPVTKVLTVEASGIQFAMAAGIALGVPFIYAKKKKAVTQSEGVYSAPVHSFTRQEDYRISISRKYLGPGDKVLIVDDFLATGAALVGLADIVNESGAELLGVGCVIEKSFQEGRSLLEDRGIAVHALARISSMSPGEIHFIGNPNTAEMIKESVEC
>NZ_LN831776.1|WP_020427423.1|7620217_7621522_-|purine-permease
MLSKQKILALGLQHVLAMYAGAVIVPLVVGGALNLSGTQMAYLIAADLFTCGLATLLQIISSKHFGSGLPVVLGCTFTAVSPIIAIASGSNLATAYGAIIISGLFVVLAAPVYGKLLKFFPTVVTGSVVTIIGLSLIPVAMNNVAGGQGSADFGAPRNLLLGLITLLVILAVNRFTTGFMRSVSVLVGLVAGTVIGYAMGIVHFSTVGSASWVSIAQPFYFGWPEFSITAIFTMIIVNIVSMVESTGVYFAVGKATDQQVEQKQVVNGLRSEGLAIMLGGLFNAFPYTAFSQNVGLLSLTRVKTRNVIFAAGGIMVVLGLLPKLAALTTVVPNAVLGGAMIVMFGSVAASGMSILSEVDLRKDGNLLIAACSIAVGLGSAVLPSMFDQLPEFARMLLQNGIVSGSLTAIILNIFLSRTQENAAPAATVPEVHVK
>NZ_LN831776.1|WP_020427422.1|7617004_7620085_-|response-regulator
MKKYWLSIAGSLLLVLILPLFSTVQLITDAQNKPVLRHGLMDLRDWDFGSDGLVRLDGEWEFYRNMLLDPEDFQPGDGPPPAASTMINVPDKWNGYISASGKRTAKGYATYRMQALITPGETAVYGLRTSNIRTASKVFMNGQEIGNSGIPSSSVSAGKQNNIPYMGFASVAGDRLEIIVQVSNYSYSSGGIVQPVIIGDQTAILKHREFALIADGAAMCGFFILSIFLLMFSRVREGRGITLHLGLFCMSAFVYILTHGEKLIASGLPGLPYEIVLKLQLISSTLVYYYLLRYVANSINYPMPQAVMKASKFITSLLLVIAVCVPAYYFSFLETLLLTWGSVSLSFVLYVMVKGTKQQPKNMFLMMVSIESLSVVILYYLISISRVHLSYNVVSYEIVLFGFVQAIVMTRKYKSSFLEVEQLSRRLVTLDGLKDDFMADTSYELRKPLQGIVNMAQTLAEGASGSLSPQQKGQLSMIVSTGKRLGSLINDMADFAKLNHGDLFLKRQAVDLRMVASSVMEVTSHISARRGLEFRLELPEPLPLLETDEERLSQILFNLLANAVNHTHKGVITLSAKVIEEYVAVIVADTGQGIAPERLGTIFDAYDPDAADAKKIYHELGLGLSITQKLVELNGGRIEVQSTPGEGSEFTFTLPILKEKTAFTDQEVLEPTGWETAAAMEMEGGLPPHLLGGEECCFILIVDNDPVNRQVLANALRLENHTVITAESGPEALLQMRDFPELDLIITDWVMPGMSGFVLCKAIRERFVLSELPILVLTASNRPEDIQAAFEAGANDYLSTPVDLREFKARVRTLLDMRKSIRTSVQTEIAFLQAQIKPHFLYNALNAIISVCPDDPDMATELLLDLSQYLRSSFDFQNRGQTVPIEKELELVRSYLALEKARFDDRLNIVFDLPQDTMALVPPLSIQPIVENAVNHGLMQKESGGTVTLSIRQLPGHLVVAVTDDGIGMTQERIADILSDERTEGGIGLRNIQRRLLKMYGAGLSVISMPDQGTTISYTIPRTGTP
>NZ_LN831776.1|WP_020427421.1|7615849_7616974_-|response-regulator
MKAILIDDEKPALQHLERLLAKDGRLEISGKYTSARLGLQHLQQERADIVFLDIGMPEMNGLEAAEHIAVLDRSIRIVYITAYSEYAIEAFELNAIDYLLKPVTSQRLGKTLERLQSREKQSAREAESAAEARALSILGFRRLEFLDTSEPGRKLQWRTSKAQEVFALLLHNRGQWILKDTIVDLVWPDFKPEKAVTNLHTTVYHIRKLLKTWGMNVLVEFSQERYRLTYEDVSFDVEDFVRGWCGTPVETDQEWASRDKVLSLYRGDYLDEHHYDWAEPKRKELQTAYVQMALRSAEYELGSARPREALTRLLSLQEVDPYSEEICRLALRSYADLGDFVGFRKHYEKFKALLHNELGIHPGSLMDSWVQRVL
>NZ_LN831776.1|WP_020427420.1|7614420_7615770_-|MFS-transporter
MNDKVVMPLWTFCLFIVVMNTTMFNVSLPTIIQDLHISADLGSWVISSYSIGYALSTVIYSRLSDLVPLRRLLTVGLTTLGLASVIGLFAHSFNVLLITRILQSAGAGVMAGLGLVLASRYVPVARRGATIAMISVGSAMAFGLGPIVGGLISQYFGWNGLFGVTCLVLLVLPVLLYLLPKEQPQAAVFDLYGAALTVINAGSLLVAVTSQSYIWLAVSVASFAVHAIHLRRARDSFINPKLLQMPGYLKLTAIGFSILVLNLGNLFLMPLALSNLFHQSALMIGLYIAPGAILSAFLTRFVGRWIDRYGNLRFLLIGHGILATVLAVFALGLQVSPLVLLFGYLCFSPAFSATMASLNNEASGILPRTWIGSGMGLLQLIQFFGGSVSVAVCGLLLHAQRTLAPSGAYRNVYGILLAVSLCSLSLVLLYRRSRGMEMKRNGAKSVSEA
>NZ_LN831776.1|WP_039786996.1|7614175_7614382_-|hypothetical-protein
MNVILFEKMPEGELRVIEERTWSMNMVAALEHVNYIVVGSREYEAVEGRLNVDAGKLELLLVPMRTEE
>NZ_LN831776.1|WP_046507758.1|7613423_7614110_-|hypothetical-protein
MKESAASRLFTPDGKPLRVLSTSLGIALLANALFIPGGTGAASGSSEEPKLVSWSTEEVKAYFDKNVDWNIPYPEENAGEVLQEGQGVVTSGGTTVINNYGGYNSGFGWDDLLLYHMLFNSGSFYSSRGWYNDRPTYYGGTRTKYKAPSYNSGSFQNKPVAGSVVKPRTSTSSTGSITRRNTSSKAGGVGGKSSGLGSSKSGSSSSKSGSTSRSSAGKSSSGKSGFGG
>NZ_LN831776.1|WP_020427417.1|7612209_7613427_-|glutathionylspermidine-synthase-family-protein
MSPADSVFEYLDQSGLERAPRVEQLHKLGFTWADLEDEEYWLDAVAVMRGETYKELEEASVKLWSILDKAVRYVHRRHDLYDLLGIPPVLWQMLDDTPLPEPGLISRYARFDFAIAGDGTIKLLELNADTPTGYVEASVATPWICGQAGISSRNNGMKERLAAAWSIEQPDTAACVAYGTHQEDSGTIEALVAHSGLDIRCVDCLDLWIDEGTVRDAENRIIKRMFALYPKEWMAVDDGGEALAYAIESGQLQLFNGPHSILLQSKGLIAAVWGMYELGLLFSEDERQAIASYILPTYNKPVFSGSFVSKSVFGREGGSVRIFDDSGALELADEDGFDSSVLFPTVYQKRAELARIQTPEGELHLLTGMFVINGVPCGLLGRAGGPITGNASHFIALGVRELEDE
>NZ_LN831776.1|WP_020427416.1|7611560_7612223_-|hypothetical-protein
MKMNKDRNRWSGRYSKVRAGAMLGMLLMAVLLLGACSGNTGSVFHTDTESTDSVSRVPWDYRVVEGTVGDLIGSDMTVLPDNEMLPNDGNYATGDKIWTLQFMDAELVTDADQKNDIRLSSWTTIKSYADQKTAAEDLTRLKVSITTDVDLVGVYKTEYKNKTRNFAVVELPSGNRIKQPIDDKRYKALEKQKKASVVLEEVHDFADYDSAYAKFRGWAN
>NZ_LN831776.1|WP_020427415.1|7611171_7611564_-|DUF350-domain-containing-protein
MTIVINLVVSVLTIILLQVLGMVVFTLMTPFKDMDELKKGNVAVALALGGKFLATAIILGVAAYTNTSIWFMMLWFAVGYVCLIAAYWIFELFTPGFKISDHLKQGNVAVGVMLCLVFVGTAFAVSSLII
>NZ_LN831776.1|WP_020427425.1|7623055_7623610_+|hypothetical-protein
MARPTQKRQDRIIVIIQKGSRKIITRTPLAGVDRLVFVINNQYTNAANTTQIASGAGRSSASGSNAAIASPFTRQQQSVGAGGDATNLGSRGQRGSKPHFPLPSLHGKEVVVVINNQTVKLPKGSKTSSATQVGSGGGTYSAGGTNAAIDSPATRQQQAVGGGTGGHALNKASSKRRRSSRRLR
>NZ_LN831776.1|WP_081487140.1|7623764_7623947_+|response-regulator
MDVLMPEMDGFETAKRIKMRRKSRDIPIIFLTALTKRPSTACSRWNSLSRIRALVFRKIK
>NZ_LN831776.1|WP_020427426.1|7623886_7624138_+|ATP-binding-protein
MLTLEFTVEDTGIGIPQDKMSYLFQPFTQISSTINRKFGGTGLGLSICKMLVELMGGEIYAKPDAGQGAVFVFTIQVSEGQPD
>NZ_LN831776.1|WP_085981544.1|7624252_7624912_-|S-layer-protein
MTSTAAAVLLTLAFAGQSLAAAAMFQDLSGTPAKDKIAQLQQRGVIHGVSDTQFMPNAAVTAAQAIQMFVNAFDLNIDLLRFVKAPQATDYFANAINDAWYANALIIAANNDIGLSPDLNPAKNWTREEFTHQLMLTIEKHSNLPLIKIMPVDIADSADFTNGYDGSIQRALVLHIASLDSDGKFHPAAGITRAEAAEMIYNALEYIAAHPAPAGGLQE
>NZ_LN831776.1|WP_085981542.1|7625021_7625384_-|winged-helix-turn-helix-transcriptional-regulator
MMAKKYNISVEATLEVIGGKWKCVILCHLTHGKMRTSDLKRHMPNITQKMLTQQLRELEQDGIVNRISYNQVPPKVEYELSDYGRTLQSILDSLCAWGEQHIIKQYGDKFAVLEDNVLNR
>NZ_LN831776.1|WP_020427429.1|7625520_7626726_+|MFS-transporter
MSLDRKKSTLALLALAISAFAIGTTEFISVGLLPLISDDLHISVTTAGLTVTLYALGVTFGAPVLTSLTTAISRKTLLLALMLLFIAGNSLAAAAGGISMLLAARILSALSHGLFMSIASTIAADLVTEDRRASAISMMFTGLTVATVTGVPLGTFLGQQLGWRAAFIAIAAVGLIALIANLLLVPAALRKGTRTPLREQVKLVTNGRLLLAFAITALGYGGTFVVFTYLSPLLHEISGFQEQTVAVILLVYGIAIAIGNVIGGKAANRKPLNALFYMFAFQAAVLLVLTFTAPFKAAALITIFFMGLLAFMNVPGLQVYVVMLADRFAPSARDVASAVNIAAFNAGIAIGAYLGGLVTDHLGLVHTPWIGSIMVLGAVVLTAWSRALENRDGRKLQSQAA
>NZ_LN831776.1|WP_020427430.1|7626890_7627733_+|aldo/keto-reductase
MALHLQDTTRLNSGVNMPWFGLGVFQVEEGAELIQAVKSAIAYGYRSVDTAAIYQNERGVGQAVAEALAENQLAREDLFITSKVWNADLGYEATLAAYDASLEKLGLDYLDLYLIHWPVQGKYKDAWRALETLYTSGRVKAIGVSNFQIHHLEDVIRDAKITPMVNQVELHPYLSQRELRRFCKEQGIQIEAWSPLMQGQLLDQPVLKEIAAAHGKSVAQVILRWDLQHGIVTIPKSTKEHRIIENASVFDFELSTGDMERIDGLNQDKRTGPDPDHFDF
>NZ_LN831776.1|WP_020425574.1|7628455_7629733_-|IS91-family-transposase
MKNQETWKKRGIIRQILKDHFHGFMEMHGHHLPKGLHSSITETVNKAIRCGTRDMGYARYECKGCTKGAPEPVFICFTCKSRFCHGCGKKYTDEWAEKQQERILNVPHRHMVFTVPQELRKVFFQDRHKLNELSKQVAKVIQYYYRRKNKSKKYEVGVITVIHTFGRDLKFNPHIHTLITEGALEQNKEWKKVEYISYEYLRKAWQKLLLDLMMKWYPKEEWIKGLVNELYQRYPQGFYVNAEQRMKDARGAAKYIGRYLARPAIAEYRVVSYDYHKVHYWYKDHRTGKRVDVVSPVMKFIYDLVQHIPPKHFRMVGRYGLYSRGKNKESQKVINLWRFMVHKQIEMTFPAEERKKKSYRQRMLESYGRDPMRCPCCKHRMLLVVIWHAEYGRIYYYDEEREYANQKKWGMRKGGKSTRTKERTG
>NZ_LN831776.1|WP_020425833.1|7630607_7631537_-|AEC-family-transporter
MIDKVLSTLVEVIVPLSIPVISGALLGRYKNLDTKPLLTLYLYFLSPAIILDTLATAEISFGDVYKTLAFSLMNLLVLWALAKLLGRVLKLAPAEAAGLTLISTFTNSVNYGLPLVLLAFGQLGLDKASVYVIAQMVIVNTIGVYFAARSQFSAGSAVRSVFSLPAIYAAILALLLRALGLHMPQEIASGVSMVAGAYSPVVLAILGVQMVRVQTAQVARNVQLAFWTGMSVRLLLAPLSAALLLVLLNISGTLFAVLLILASMPVAVNSVVLAERFGSSPALVSRCILWTTLASFLVLPILISIVGSV
>NZ_LN831776.1|WP_020425834.1|7631713_7632052_+|helix-turn-helix-transcriptional-regulator
MDNTEPVILTKGTPGEACPIAKTLDVIGTKWTFLIIRDLLIEGTMRFSDLLRSLEGISPKTLALRLRELESHGILMRTVYPEVPPRVEYTLTKKGEQLEGIFIELKRYGLAL

Crispr_ID: NZ_LN831776_77

• CRISPR_ID: NZ_LN831776_77
• CRISPR_location: 7629902-7629976
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_77

Consensus_repeat	Method
AAGTGGAAAAAGGTACACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_77

>77.1|7629925|29|NZ_LN831776|CRISPRCasFinder
TGCCGAAGTACCCTACCCTCGGGCAGATG

CRISPR arrays and Neighbor proteins around NZ_LN831776_77

CRISPR arrays

The CRISPR arrays of NZ_LN831776_77

>merge|NZ_LN831776|77|7629902-7629976|CRISPRCasFinder
AAGTGGAAAAAGGTACACTAATTTGCCGAAGTACCCTACCCTCGGGCAGATGAAGTGGAAAAAGGGACACTAATT

>NZ_LN831776|77|77|7629902-7629976|CRISPRCasFinder
AAGTGGAAAAAGGTACACTAATT	TGCCGAAGTACCCTACCCTCGGGCAGATG
AAGTGGAAAAAGGGACACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020425840.1|7637650_7638820_+|ATP-grasp-domain-containing-protein	unknown	unknown	gnl|CDD|316093
NZ_LN831776.1|WP_020425842.1|7639736_7640024_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425835.1|7632207_7632927_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|235914
NZ_LN831776.1|WP_020427425.1|7623055_7623610_+|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425836.1|7633120_7633600_-|transcription-elongation-factor-GreA	unknown	unknown	gnl|CDD|234693
NZ_LN831776.1|WP_020425838.1|7635397_7636879_-|multidrug-efflux-MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_LN831776.1|WP_046507768.1|7637103_7637586_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224759
NZ_LN831776.1|WP_020427424.1|7621515_7622130_-|xanthine-phosphoribosyltransferase	unknown	unknown	gnl|CDD|181705
NZ_LN831776.1|WP_020425574.1|7628455_7629733_-|IS91-family-transposase	unknown	unknown	gnl|CDD|377437
NZ_LN831776.1|WP_020425834.1|7631713_7632052_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224647
NZ_LN831776.1|WP_020425833.1|7630607_7631537_-|AEC-family-transporter	unknown	unknown	gnl|CDD|223751
NZ_LN831776.1|WP_020427429.1|7625520_7626726_+|MFS-transporter	unknown	unknown	gnl|CDD|225371
NZ_LN831776.1|WP_020427426.1|7623886_7624138_+|ATP-binding-protein	unknown	unknown	gnl|CDD|340399
NZ_LN831776.1|WP_020427430.1|7626890_7627733_+|aldo/keto-reductase	unknown	unknown	gnl|CDD|381383
NZ_LN831776.1|WP_081487140.1|7623764_7623947_+|response-regulator	unknown	unknown	gnl|CDD|381147
NZ_LN831776.1|WP_085981544.1|7624252_7624912_-|S-layer-protein	unknown	unknown	gnl|CDD|306825
NZ_LN831776.1|WP_085981542.1|7625021_7625384_-|winged-helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|334619
NZ_LN831776.1|WP_020425841.1|7638833_7639583_+|esterase-family-protein	unknown	unknown	gnl|CDD|227283
NZ_LN831776.1|WP_020427423.1|7620217_7621522_-|purine-permease	unknown	unknown	gnl|CDD|274468
NZ_LN831776.1|WP_020425837.1|7633808_7635245_+|FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|378963

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020425840.1|7637650_7638820_+|ATP-grasp-domain-containing-protein	gnl|CDD|316093	pfam13535, ATP-grasp_4, ATP-grasp domain. This family includes a diverse set of enzymes that possess ATP-dependent carboxylate-amine ligase activity.	7.5397e-13
NZ_LN831776.1|WP_020425835.1|7632207_7632927_+|SDR-family-oxidoreductase	gnl|CDD|235914	PRK07041, PRK07041, SDR family oxidoreductase.	8.40133e-86
NZ_LN831776.1|WP_020425836.1|7633120_7633600_-|transcription-elongation-factor-GreA	gnl|CDD|234693	PRK00226, greA, transcription elongation factor GreA; Reviewed.	6.70403e-65
NZ_LN831776.1|WP_020425838.1|7635397_7636879_-|multidrug-efflux-MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	6.86357e-86
NZ_LN831776.1|WP_046507768.1|7637103_7637586_+|MarR-family-transcriptional-regulator	gnl|CDD|224759	COG1846, MarR, Transcriptional regulators [Transcription].	5.71227e-14
NZ_LN831776.1|WP_020427424.1|7621515_7622130_-|xanthine-phosphoribosyltransferase	gnl|CDD|181705	PRK09219, PRK09219, xanthine phosphoribosyltransferase; Validated.	1.24864e-96
NZ_LN831776.1|WP_020425574.1|7628455_7629733_-|IS91-family-transposase	gnl|CDD|377437	pfam04986, Y2_Tnp, Putative transposase. Transposases are needed for efficient transposition of the insertion sequence or transposon DNA. This family includes transposases IS1294 and IS801. This is a rolling-circle transposase.	1.83895e-38
NZ_LN831776.1|WP_020425834.1|7631713_7632052_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	5.38779e-37
NZ_LN831776.1|WP_020425833.1|7630607_7631537_-|AEC-family-transporter	gnl|CDD|223751	COG0679, COG0679, Predicted permeases [General function prediction only].	3.60877e-34
NZ_LN831776.1|WP_020427429.1|7625520_7626726_+|MFS-transporter	gnl|CDD|225371	COG2814, AraJ, Arabinose efflux permease [Carbohydrate transport and metabolism].	3.63307e-102
NZ_LN831776.1|WP_020427426.1|7623886_7624138_+|ATP-binding-protein	gnl|CDD|340399	cd16922, HATPase_EvgS-ArcB-TorS-like, Histidine kinase-like ATPase domain of two-component sensor histidine kinases, many are hybrid sensor histidine kinases, similar to Escherichia coli EvgS, ArcB, TorS, BarA, RcsC. This family contains the histidine kinase-like ATPase (HATPase) domains of various two-component hybrid sensor histidine kinases (HKs), including the following Escherichia coli HKs: EvgS, a HK of the EvgS-EvgA two-component system (TCS) that confers acid resistance; ArcB, a HK of the ArcB-ArcA TCS that modulates the expression of numerous genes in response to respiratory growth conditions; TorS, a HK of the TorS-TorR TCS which is involved in the anaerobic utilization of trimethylamine-N-oxide; BarA, a HK of the BarA-UvrY TCS involved in the regulation of carbon metabolism; and RcsC, a HK of the RcsB-RcsC TCS which regulates the expression of the capsule operon and of the cell division gene ftsZ. Proteins having this HATPase domain also contain a histidine kinase dimerization and phosphoacceptor domain (HisKA), with most having accessory sensor domain(s) such as GAF, PAS and CHASE; many are hybrid sensor histidine kinases as they also contain a REC signal receiver domain.	1.2557e-34
NZ_LN831776.1|WP_020427430.1|7626890_7627733_+|aldo/keto-reductase	gnl|CDD|381383	cd19157, AKR_AKR5G1-3, AKR5G family of aldo-keto reductase (AKR). Bacillus subtilis glyoxal reductase (GR), uncharacterized oxidoreductase YtbE, and Bacillus aryabhattai aldo-keto reductase are founding members of aldo-keto reductase family 5 member G1-3 (AKR5G1-3), respectively. GR (YvgN, EC 1.1.1.283), also called methylglyoxal reductase, reduces glyoxal and methylglyoxal (2-oxopropanal). It is not involved in vitamin B6 biosynthesis.	0
NZ_LN831776.1|WP_081487140.1|7623764_7623947_+|response-regulator	gnl|CDD|381147	cd19920, REC_PA4781-like, phosphoacceptor receiver (REC) domain of cyclic di-GMP phosphodiesterase PA4781 and similar domains. Pseudomonas aeruginosa cyclic di-GMP phosphodiesterase PA4781 contains an N-terminal REC domain and a C-terminal catalytic HD-GYP domain, characteristics of RpfG family response regulators. PA4781 is involved in cyclic di-3',5'-GMP (c-di-GMP) hydrolysis/degradation in a two-step reaction via the linear intermediate pGpG to produce GMP. Its unphosphorylated REC domain prevents accessibility of c-di-GMP to the active site. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.25805e-14
NZ_LN831776.1|WP_085981544.1|7624252_7624912_-|S-layer-protein	gnl|CDD|306825	pfam00395, SLH, S-layer homology domain.	0.000123195
NZ_LN831776.1|WP_085981542.1|7625021_7625384_-|winged-helix-turn-helix-transcriptional-regulator	gnl|CDD|334619	pfam01638, HxlR, HxlR-like helix-turn-helix. HxlR, a member of this family, is a DNA-binding protein that acts as a positive regulator of the formaldehyde-inducible hxlAB operon in Bacillus subtilis.	2.02228e-48
NZ_LN831776.1|WP_020425841.1|7638833_7639583_+|esterase-family-protein	gnl|CDD|227283	COG4947, COG4947, Uncharacterized protein conserved in bacteria [Function unknown].	3.17062e-88
NZ_LN831776.1|WP_020427423.1|7620217_7621522_-|purine-permease	gnl|CDD|274468	TIGR03173, pbuX, xanthine permease. All the seed members of this model are observed adjacent to genes for either xanthine phosphoribosyltransferase (for the conversion of xanthine to guanine, GenProp0696) or genes for the conversion of xanthine to urate and its concomitant catabolism (GenProp0640, GenProp0688, GenProp0686 and GenProp0687). A number of sequences scoring higher than trusted to this model are found in different genomic contexts, and the possibility exist that these transport related compounds in addition to or instead of xanthine itself. The outgroup to this family are sequences which are characterized as uracil permeases or are adjacent to established uracil phosphoribosyltransferases.	1.18101e-172
NZ_LN831776.1|WP_020425837.1|7633808_7635245_+|FAD-dependent-oxidoreductase	gnl|CDD|378963	pfam12831, FAD_oxidored, FAD dependent oxidoreductase. This family of proteins contains FAD dependent oxidoreductases and related proteins.	1.94884e-24

Protein sequences

>NZ_LN831776.1|WP_020425574.1|7628455_7629733_-|IS91-family-transposase
MKNQETWKKRGIIRQILKDHFHGFMEMHGHHLPKGLHSSITETVNKAIRCGTRDMGYARYECKGCTKGAPEPVFICFTCKSRFCHGCGKKYTDEWAEKQQERILNVPHRHMVFTVPQELRKVFFQDRHKLNELSKQVAKVIQYYYRRKNKSKKYEVGVITVIHTFGRDLKFNPHIHTLITEGALEQNKEWKKVEYISYEYLRKAWQKLLLDLMMKWYPKEEWIKGLVNELYQRYPQGFYVNAEQRMKDARGAAKYIGRYLARPAIAEYRVVSYDYHKVHYWYKDHRTGKRVDVVSPVMKFIYDLVQHIPPKHFRMVGRYGLYSRGKNKESQKVINLWRFMVHKQIEMTFPAEERKKKSYRQRMLESYGRDPMRCPCCKHRMLLVVIWHAEYGRIYYYDEEREYANQKKWGMRKGGKSTRTKERTG
>NZ_LN831776.1|WP_020427430.1|7626890_7627733_+|aldo/keto-reductase
MALHLQDTTRLNSGVNMPWFGLGVFQVEEGAELIQAVKSAIAYGYRSVDTAAIYQNERGVGQAVAEALAENQLAREDLFITSKVWNADLGYEATLAAYDASLEKLGLDYLDLYLIHWPVQGKYKDAWRALETLYTSGRVKAIGVSNFQIHHLEDVIRDAKITPMVNQVELHPYLSQRELRRFCKEQGIQIEAWSPLMQGQLLDQPVLKEIAAAHGKSVAQVILRWDLQHGIVTIPKSTKEHRIIENASVFDFELSTGDMERIDGLNQDKRTGPDPDHFDF
>NZ_LN831776.1|WP_020427429.1|7625520_7626726_+|MFS-transporter
MSLDRKKSTLALLALAISAFAIGTTEFISVGLLPLISDDLHISVTTAGLTVTLYALGVTFGAPVLTSLTTAISRKTLLLALMLLFIAGNSLAAAAGGISMLLAARILSALSHGLFMSIASTIAADLVTEDRRASAISMMFTGLTVATVTGVPLGTFLGQQLGWRAAFIAIAAVGLIALIANLLLVPAALRKGTRTPLREQVKLVTNGRLLLAFAITALGYGGTFVVFTYLSPLLHEISGFQEQTVAVILLVYGIAIAIGNVIGGKAANRKPLNALFYMFAFQAAVLLVLTFTAPFKAAALITIFFMGLLAFMNVPGLQVYVVMLADRFAPSARDVASAVNIAAFNAGIAIGAYLGGLVTDHLGLVHTPWIGSIMVLGAVVLTAWSRALENRDGRKLQSQAA
>NZ_LN831776.1|WP_085981542.1|7625021_7625384_-|winged-helix-turn-helix-transcriptional-regulator
MMAKKYNISVEATLEVIGGKWKCVILCHLTHGKMRTSDLKRHMPNITQKMLTQQLRELEQDGIVNRISYNQVPPKVEYELSDYGRTLQSILDSLCAWGEQHIIKQYGDKFAVLEDNVLNR
>NZ_LN831776.1|WP_085981544.1|7624252_7624912_-|S-layer-protein
MTSTAAAVLLTLAFAGQSLAAAAMFQDLSGTPAKDKIAQLQQRGVIHGVSDTQFMPNAAVTAAQAIQMFVNAFDLNIDLLRFVKAPQATDYFANAINDAWYANALIIAANNDIGLSPDLNPAKNWTREEFTHQLMLTIEKHSNLPLIKIMPVDIADSADFTNGYDGSIQRALVLHIASLDSDGKFHPAAGITRAEAAEMIYNALEYIAAHPAPAGGLQE
>NZ_LN831776.1|WP_020427426.1|7623886_7624138_+|ATP-binding-protein
MLTLEFTVEDTGIGIPQDKMSYLFQPFTQISSTINRKFGGTGLGLSICKMLVELMGGEIYAKPDAGQGAVFVFTIQVSEGQPD
>NZ_LN831776.1|WP_081487140.1|7623764_7623947_+|response-regulator
MDVLMPEMDGFETAKRIKMRRKSRDIPIIFLTALTKRPSTACSRWNSLSRIRALVFRKIK
>NZ_LN831776.1|WP_020427425.1|7623055_7623610_+|hypothetical-protein
MARPTQKRQDRIIVIIQKGSRKIITRTPLAGVDRLVFVINNQYTNAANTTQIASGAGRSSASGSNAAIASPFTRQQQSVGAGGDATNLGSRGQRGSKPHFPLPSLHGKEVVVVINNQTVKLPKGSKTSSATQVGSGGGTYSAGGTNAAIDSPATRQQQAVGGGTGGHALNKASSKRRRSSRRLR
>NZ_LN831776.1|WP_020427424.1|7621515_7622130_-|xanthine-phosphoribosyltransferase
MKILEERIREEGLILSDTVLKVDSFLNHQVDTQLALQIGEEFGRIFGHLPVTKVLTVEASGIQFAMAAGIALGVPFIYAKKKKAVTQSEGVYSAPVHSFTRQEDYRISISRKYLGPGDKVLIVDDFLATGAALVGLADIVNESGAELLGVGCVIEKSFQEGRSLLEDRGIAVHALARISSMSPGEIHFIGNPNTAEMIKESVEC
>NZ_LN831776.1|WP_020427423.1|7620217_7621522_-|purine-permease
MLSKQKILALGLQHVLAMYAGAVIVPLVVGGALNLSGTQMAYLIAADLFTCGLATLLQIISSKHFGSGLPVVLGCTFTAVSPIIAIASGSNLATAYGAIIISGLFVVLAAPVYGKLLKFFPTVVTGSVVTIIGLSLIPVAMNNVAGGQGSADFGAPRNLLLGLITLLVILAVNRFTTGFMRSVSVLVGLVAGTVIGYAMGIVHFSTVGSASWVSIAQPFYFGWPEFSITAIFTMIIVNIVSMVESTGVYFAVGKATDQQVEQKQVVNGLRSEGLAIMLGGLFNAFPYTAFSQNVGLLSLTRVKTRNVIFAAGGIMVVLGLLPKLAALTTVVPNAVLGGAMIVMFGSVAASGMSILSEVDLRKDGNLLIAACSIAVGLGSAVLPSMFDQLPEFARMLLQNGIVSGSLTAIILNIFLSRTQENAAPAATVPEVHVK
>NZ_LN831776.1|WP_020425833.1|7630607_7631537_-|AEC-family-transporter
MIDKVLSTLVEVIVPLSIPVISGALLGRYKNLDTKPLLTLYLYFLSPAIILDTLATAEISFGDVYKTLAFSLMNLLVLWALAKLLGRVLKLAPAEAAGLTLISTFTNSVNYGLPLVLLAFGQLGLDKASVYVIAQMVIVNTIGVYFAARSQFSAGSAVRSVFSLPAIYAAILALLLRALGLHMPQEIASGVSMVAGAYSPVVLAILGVQMVRVQTAQVARNVQLAFWTGMSVRLLLAPLSAALLLVLLNISGTLFAVLLILASMPVAVNSVVLAERFGSSPALVSRCILWTTLASFLVLPILISIVGSV
>NZ_LN831776.1|WP_020425834.1|7631713_7632052_+|helix-turn-helix-transcriptional-regulator
MDNTEPVILTKGTPGEACPIAKTLDVIGTKWTFLIIRDLLIEGTMRFSDLLRSLEGISPKTLALRLRELESHGILMRTVYPEVPPRVEYTLTKKGEQLEGIFIELKRYGLAL
>NZ_LN831776.1|WP_020425835.1|7632207_7632927_+|SDR-family-oxidoreductase
MLTGQKIVIIGGSSGIGLATAKLAAAEGAEVVLASRSAQKLEQAAAALGPAASVATYTLDITSEAQVQSLFAELGAFDHLVITAAETSGGPFLTTATRAARQLMDNKFWGQYYAAKYAAPHLNPHGSITLFSGVVAFKAMTGSSVLGAVNAAVANLGQTLALELAPLRVNTVSPGIIDTPSRAGMAEEARSAFYSSVAAKLPVKRVGTASDVAEGVLYLIRNGFVTGTVLHVEGGHTLI
>NZ_LN831776.1|WP_020425836.1|7633120_7633600_-|transcription-elongation-factor-GreA
MSNEEVFLTKEGLAKLEEELRDLKTVKRKELAARLKLAISYGDLKENSEYHSAKEDQSFMETRIMILEKMLTKAQIVDESSMDLSKVSVGSLVTLNDVEYSEKIEYRVVGPAEADVLDNKISYESPLGKELLGKKVGDIISVNAPMGIIQYELLEIKLL
>NZ_LN831776.1|WP_020425837.1|7633808_7635245_+|FAD-dependent-oxidoreductase
MFMQSRKFHRIKSCLAALVLLSAAVLPATAAAKPAATSTAPAGYDVVIIGSEIQGALLAKEAVKAGLKVLMLDPRSKPGGELIQGQMFFLDDVNDNQKRSLVQGEIKNLLNGYKAGTIRNAADFQKYYNKVMQGIPLKSGIVLDRVDTKETSSGKMLSALTYHGKDGVKATIQSRYWVENTDYNALSGKLKEARIPGMETIYNSTVPDYMAATYMLNFKNVDWNLLHQRILEDYPLTNVRKKYGPNTYVDWHFATGFSNITNRYATKDRQLRLRGLNASYQKNGQVIINGLLIYDVNPADPKSVESAVRKGKAEAPYILSFLRKNIPGFAKAELNGFPEYLYIRDYNRYETKYVLEYTDLMSSRMFWDNVSIGGYSIDLQGTRAIPTGIGFGKPDRYGLPLRSFELKSYDNVLVTGKNVGASIKAYGSARIMPTTALAAQTIGIILGRERSKRLDDLNVEDFKRIRAYLKKDYQISLQ
>NZ_LN831776.1|WP_020425838.1|7635397_7636879_-|multidrug-efflux-MFS-transporter
MNNHTARNSSFWLIILAVFFGNFMAILSTTTINVAFPVFMKDFHAEIGTVQWMITGYLLATGVIAPVVGYFGDKWSYKYLYVFALSGFTLFSGLCMIAWSIHSLVIFRILQGVFGGLIIPTTMTMIYQFIEKEKQAFAMSLWSLSSMLAPALGPTLGGWLTGYFGWESLFMINLPIGIIAIAVALKCLPFQRNAGETKSFDLPGFVTVILSSAFIILAFNKGNSWGWTSWKVLALLIIGAVALMYFIRRELSLKEPLLNLKVFRQNRFTYSLIINCIITVALYSGTFLIPVFLQDIQQSTPLTTALVLLPGSIAMAVMSPVVGKLYSKVGPFWLILGGILLLAASTWELSHLTLATTHVQLAWLMAVRNIGIALAFMPVTNAGMSSVPKQITGHASSVTNWVRQATGALSIAIFSSLLASRALTHQKELSGGASAAGALIKAQGMTMGVQDVFLTATVIGILAIPLTFLLRTGTAKPQAAVLNVATVKRGANS
>NZ_LN831776.1|WP_046507768.1|7637103_7637586_+|MarR-family-transcriptional-regulator
MDVKKDDKNLESLNNELMTLIRRSSLDKKHGGLDRSTYTLLYHLAHHEKVGVKALAEEFGLDTSTISRQTSVLEAKGYAVRVPDPMDGRSSYFEITLLGTRKLEEARNIRLERYGEIFADWSPEDCHTFSGLLARLNRKLAQRSADAKGLTEEAEAGRLN
>NZ_LN831776.1|WP_020425840.1|7637650_7638820_+|ATP-grasp-domain-containing-protein
MNFIFFSPHFPRNSADFCSQLHQQGATVLGIGDAEYDQLEDKLKSALTEYYKVSSLENHGEILRAVGYFTHQYGKIDRFESLNEYWLEQDAAIRTDFNIYGTKTDFVYNLKQKSKMKEFFRKSGVSTVQFSTGTTRDSVQDFIRSTGFPLVVKPDLGSGASMTYKINNEAELQQFFDTKPDDVAFIIEEFIDGVILTYDGLVDIEGNVRFAASHLFENSVMDVVNTDNHLYYFCLKDVSPEVELAGRNILKAFDIKERFFHIELFKSNMDGRIIALEVNMRPPGAWMTDAINFSYDVDVYREWARMVVHNEVSGPFEGKYYTGYASRKQHKHYSHSHEDIYRMYGDKIVNYAGIEEVFSRAMGNSAYQFRSADLADVRDIVNYIQQEEG
>NZ_LN831776.1|WP_020425841.1|7638833_7639583_+|esterase-family-protein
MRISYHKEYSHHLHRDMEYKVYGHAGKPMLVFPTSLGRFYQYEDSGMIQTLSEFIDAGKLQIWACDTLDEETFFSSHWNHEDKVYRHEQYDKYIMQELIPGILHSSKENNGGSDQKLLISGCSMGAYYSASFFFRHPHVFDTLIALSGVYSTYYFFGDYMSETVYLNSPLHYLPNLTDDDYLNAYRSSRIILCVGQGAYEDEMLHETRLLQDLLQRKHIPAQIEYWGHDVDHDWPWWNKQIHYYVGGCL
>NZ_LN831776.1|WP_020425842.1|7639736_7640024_-|hypothetical-protein
MLTFTSYTVENVRDPFGILSGKRYEFVINLDVPEEDELYEENGVSARVIVKVEDEEASIINYDLLETTTGRLLDFDMEEDEEAALVLFCKEHLPA

Crispr_ID: NZ_LN831776_78

• CRISPR_ID: NZ_LN831776_78
• CRISPR_location: 7662621-7662695
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_78

Consensus_repeat	Method
AAGTGGAAAAAGGGACACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_78

>78.1|7662644|29|NZ_LN831776|CRISPRCasFinder
TGCCGAAGTACCCTATCCTCGGGCAGATG

CRISPR arrays and Neighbor proteins around NZ_LN831776_78

CRISPR arrays

The CRISPR arrays of NZ_LN831776_78

>merge|NZ_LN831776|78|7662621-7662695|CRISPRCasFinder
AAGTGGAAAAAGGGACACTAATTTGCCGAAGTACCCTATCCTCGGGCAGATGAAGTGGAAAAAGGGACACTAATT

>NZ_LN831776|78|78|7662621-7662695|CRISPRCasFinder
AAGTGGAAAAAGGGACACTAATT	TGCCGAAGTACCCTATCCTCGGGCAGATG
AAGTGGAAAAAGGGACACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020426207.1|7665831_7666263_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_LN831776.1|WP_020426213.1|7670095_7671310_-|chromate-transporter	unknown	unknown	gnl|CDD|273350
NZ_LN831776.1|WP_051010594.1|7666281_7667715_-|DHA2-family-efflux-MFS-transporter-permease-subunit	unknown	unknown	gnl|CDD|129794
NZ_LN831776.1|WP_020425982.1|7661403_7662510_+|GIY-YIG-nuclease-family-protein	unknown	unknown	gnl|CDD|234792
NZ_LN831776.1|WP_020426204.1|7663164_7664022_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|187578
NZ_LN831776.1|WP_020425986.1|7657029_7657737_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426206.1|7665127_7665712_-|NAD(P)H-dependent-oxidoreductase	unknown	unknown	gnl|CDD|225158
NZ_LN831776.1|WP_020425985.1|7658000_7658222_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020425987.1|7655526_7656948_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_081487086.1|7668230_7668905_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_LN831776.1|WP_020425984.1|7658327_7660319_-|FAD-binding-protein	unknown	unknown	gnl|CDD|180854
NZ_LN831776.1|WP_039785549.1|7664289_7665135_+|NAD(+)-diphosphatase	unknown	unknown	gnl|CDD|234699
NZ_LN831776.1|WP_082118159.1|7671538_7672423_-|Abi-family-protein	unknown	unknown	gnl|CDD|377910
NZ_LN831776.1|WP_020426211.1|7669098_7669440_-|alkylphosphonate-utilization-protein	unknown	unknown	gnl|CDD|225380
NZ_LN831776.1|WP_020425983.1|7660424_7661246_-|MerR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|133378
NZ_LN831776.1|WP_020426212.1|7669599_7670088_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831776.1|WP_039787702.1|7654979_7655261_-|hypothetical-protein	unknown	unknown	unknown
NZ_LN831776.1|WP_020426167.1|7652882_7653206_+|hypothetical-protein	unknown	unknown	gnl|CDD|224278
NZ_LN831776.1|WP_020426168.1|7653293_7654130_-|EcsC-family-protein	unknown	unknown	gnl|CDD|378945
NZ_LN831776.1|WP_020426166.1|7652018_7652759_-|Bax-inhibitor-1/YccA-family-protein	unknown	unknown	gnl|CDD|378959

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020426207.1|7665831_7666263_+|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	1.33781e-15
NZ_LN831776.1|WP_051010594.1|7666281_7667715_-|DHA2-family-efflux-MFS-transporter-permease-subunit	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	3.20312e-94
NZ_LN831776.1|WP_081487086.1|7668230_7668905_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	2.67365e-10
NZ_LN831776.1|WP_020426204.1|7663164_7664022_-|SDR-family-oxidoreductase	gnl|CDD|187578	cd05269, TMR_SDR_a, triphenylmethane reductase (TMR)-like proteins, NMRa-like, atypical (a) SDRs. TMR is an atypical NADP-binding protein of the SDR family. It lacks the active site residues of the SDRs but has a glycine rich NAD(P)-binding motif that matches the extended SDRs. Proteins in this subgroup however, are more similar in length to the classical SDRs. TMR was identified as a reducer of triphenylmethane dyes, important environmental pollutants. This subgroup also includes Escherichia coli NADPH-dependent quinine oxidoreductase (QOR2), which catalyzes two-electron reduction of quinone; but is unlikely to play a major role in protecting against quinone cytotoxicity. Atypical SDRs are distinct from classical SDRs. Atypical SDRs include biliverdin IX beta reductase (BVR-B,aka flavin reductase), NMRa (a negative transcriptional regulator of various fungi), progesterone 5-beta-reductase like proteins, phenylcoumaran benzylic ether and pinoresinol-lariciresinol reductases, phenylpropene synthases, eugenol synthase, triphenylmethane reductase, isoflavone reductases, and others. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. In addition to the Rossmann fold core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	5.90313e-88
NZ_LN831776.1|WP_020425983.1|7660424_7661246_-|MerR-family-transcriptional-regulator	gnl|CDD|133378	cd00592, HTH_MerR-like, Helix-Turn-Helix DNA binding domain of MerR-like transcription regulators. Helix-turn-helix (HTH) MerR-like transcription regulator, N-terminal domain. The MerR family transcription regulators have been shown to mediate responses to stress including exposure to heavy metals, drugs, or oxygen radicals in eubacterial and some archaeal species. They regulate transcription of multidrug/metal ion transporter genes and oxidative stress regulons by reconfiguring the spacer between the -35 and -10 promoter elements. A typical MerR regulator is comprised of two distinct domains that harbor the regulatory (effector-binding) site and the active (DNA-binding) site. Their N-terminal domains are homologous and contain a DNA-binding winged HTH motif, while the C-terminal domains are often dissimilar and bind specific coactivator molecules such as metal ions, drugs, and organic substrates.	7.39873e-17
NZ_LN831776.1|WP_020426206.1|7665127_7665712_-|NAD(P)H-dependent-oxidoreductase	gnl|CDD|225158	COG2249, MdaB, Putative NADPH-quinone reductase (modulator of drug activity B) [General function prediction only].	3.36963e-37
NZ_LN831776.1|WP_020426211.1|7669098_7669440_-|alkylphosphonate-utilization-protein	gnl|CDD|225380	COG2824, PhnA, Uncharacterized Zn-ribbon-containing protein involved in phosphonate metabolism [Inorganic ion transport and metabolism].	4.31028e-67
NZ_LN831776.1|WP_020426213.1|7670095_7671310_-|chromate-transporter	gnl|CDD|273350	TIGR00937, Chromate_transport_protein, chromate transporter, chromate ion transporter (CHR) family. Members of this family probably act as chromate transporters, and are found in Pseudomonas aeruginosa, Alcaligenes eutrophus, Vibrio cholerae, Bacillus subtilis, Ochrobactrum tritici, cyanobacteria and archaea. The protein reduces chromate accumulation and is essential for chromate resistance. [Transport and binding proteins, Anions].	1.58341e-101
NZ_LN831776.1|WP_020426167.1|7652882_7653206_+|hypothetical-protein	gnl|CDD|224278	COG1359, COG1359, Uncharacterized conserved protein [Function unknown].	3.74468e-10
NZ_LN831776.1|WP_082118159.1|7671538_7672423_-|Abi-family-protein	gnl|CDD|377910	pfam07751, Abi_2, Abi-like protein. This family, found in various bacterial species, contains sequences that are similar to the Abi group of proteins, which are involved in bacteriophage resistance mediated by abortive infection in Lactococcus species. The proteins are thought to have helix-turn-helix motifs, found in many DNA-binding proteins, allowing them to perform their function.	2.68116e-54
NZ_LN831776.1|WP_039785549.1|7664289_7665135_+|NAD(+)-diphosphatase	gnl|CDD|234699	PRK00241, nudC, NAD(+) diphosphatase.	1.78412e-103
NZ_LN831776.1|WP_020426212.1|7669599_7670088_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	3.62264e-13
NZ_LN831776.1|WP_020425982.1|7661403_7662510_+|GIY-YIG-nuclease-family-protein	gnl|CDD|234792	PRK00558, uvrC, excinuclease ABC subunit UvrC.	1.01973e-67
NZ_LN831776.1|WP_020425984.1|7658327_7660319_-|FAD-binding-protein	gnl|CDD|180854	PRK07121, PRK07121, FAD-binding protein.	1.32893e-41
NZ_LN831776.1|WP_020426168.1|7653293_7654130_-|EcsC-family-protein	gnl|CDD|378945	pfam12787, EcsC, EcsC protein family. Proteins in this family are related to EcsC from B. subtilis. This protein is found in an operon with EcsA and EcsB which are components of an ABC transport system. The function of this protein is unknown.	3.90186e-78
NZ_LN831776.1|WP_020426166.1|7652018_7652759_-|Bax-inhibitor-1/YccA-family-protein	gnl|CDD|378959	pfam12811, BaxI_1, Bax inhibitor 1 like. The Bax-inhibitor-1 region of the receptor molecules is conserved from bacteria to humans.	1.15663e-94

Protein sequences

>NZ_LN831776.1|WP_020425982.1|7661403_7662510_+|GIY-YIG-nuclease-family-protein
MNLAEKVAALPLSPGVYLMKDSLGHIIYVGKAKQLKKRVQSYFYNAKGHSPKVKQLVRNIRDFDYKLTDTEFEAFMLECQLIKEIKPMYNKKMKNPLAYSYIVIRTDTAYRQLAVTYDPAEYGDSLYFGPYTSRSTVERAVQGIKESQRILCSTPHARNALCLNHSLGLCLGMCGGGEALERYEGIIDSVAGLLNGNDPRILEELQQRMDLAAENFEFETAAKYRDYCTAVRSLLQKEKVIGFTEQNKNIVVLEPMQEQVLKLILIRGSEILDRARLDAGQMNAEQLCGIIQAAVQDSFSKPPHGEPGEISRHKLDEAQIIYSYLTGSSGSYAVIPQEWLEAGDGAAVAEAVRELLGGYFEAAPAKFQ
>NZ_LN831776.1|WP_020425983.1|7660424_7661246_-|MerR-family-transcriptional-regulator
MKYSIGEFASILGVTADTLRLYEKHDIVRPMKDQHNNYRYFSDLDARNLLSSRWYRSMQIPLQDVAGLINDAPAEQVIQSIAGARQQLEEEIKRSVMLLDKINEIHAELGRIGEALYACRIREVPGMYRIQQTDKNQLLQKECLKRTVQAWMELLPFTFYSFRIENPESVLGTEELEYSWGLALLETDQRKLEVGVNESMEYIGPSTCISAVIASAYEKELGRESFQFMLDFAGAEGLAITGDIRGKILFTERMSRGNQTYLEIDIPLENNFT
>NZ_LN831776.1|WP_020425984.1|7658327_7660319_-|FAD-binding-protein
MRKQAQSKIFTLSVCLIMMLSLISGCSGNNTAEPAASEQPSASPEATQQAGDDNGVPASFKAGTYKAEADGKDGKIQVEVTLDAQSTITDIKVLNQKETAGIGVEAINKIKDEIISGQTLAIDAVSGASESSAAILTAVEDALKQAGGNVEAFKSRKVAKAGEGKTEQLSADVVVVGAGASGVSAAVSAADKGAKVIIIEKTATIGGASNLSWAGKFYNSSAAVSSGLKVSVEKEISDWIVNNHWRVDAAAIRQYVTKSGETYDWLNKKGYKTTFINFAGEQLHMLPAYETRQPTLRAMLAASVEKGGGQVITETTAKKLMTGANGEVTGVVAEKADGTTLEITGKSIIMATGGYAGNKEMVKEAFGFEGVNGGLGQNIGEGLKMAWDAGAKVPDNFGGQMLHQTLARATEKLKAEYTPFEASYPLMLSYLPTLMNVGPSGARFRDEAATLTSVAAANTSAFNGAYHLVIISQAQIDALKAKGMNGVKAPSLPGMPPEFYATFADQFKLDTPWKDADKVFESMVANGDGYKGSTIAELAQNAGLDAEVFAHDFNQYQEATKTGVDTEFGKAKEYLIPMGQSGPYYAIIAEVNNLGSVGGLLVNTQFQVLNDKRVPVKGLYAVGLESEGVLFNDTYVGNGVGLGYSFTSGRLGGEDAAAGALAK
>NZ_LN831776.1|WP_020425985.1|7658000_7658222_-|hypothetical-protein
MKKVLARIAVALLVLTIVAIVLCFYFDHFMYAYSLILVLFFIFAGMGQLYKLKNDEYMHRKLNQRDEYEDYTR
>NZ_LN831776.1|WP_020425986.1|7657029_7657737_-|hypothetical-protein
MYIPITGISGVSLTRPPQQPENHSSTPASALSFNETLAAVNAATMDQAERLKRKYGVRVRIQAVSKGGKELEHSGMSGDEREIIIAPNILQQMAKDPVMRNKVYGTLDPYVTQEQTSQNPLQPLKGGKGLNHSLIVHKDGSVALWSAAASPREAETGKHLDMENRNEQAEESRTAAERRHAWEAALPILSKNLLSAAEASLQGQEPAANPVDGVAAHDWLHQLQLVRARRSNKLL
>NZ_LN831776.1|WP_020425987.1|7655526_7656948_-|hypothetical-protein
MGIQLTAIHWVYLTFIVFIMVLMIRRRDTTMICVAGIFALGLLAAESLSGSVSGIFNSFVYATKELLGTIMIISIIVAMSRILMITGINETMVAPLTRFIRTPCMAYWGIGLIMMVTSFFFWPSPAVALVGAVLLPVALRVGLPALGAAVAMNLFGHGIALSGDYIIQGAPKITSDAAGLPVASVMEASIPLVIVMGLVTTIAAFWMMRRDRQNGTWRDGLVSVQGSTGRLRGPDAAGGEETPVLLPARLRQGLAVAIPLLFLLDVAAMFALNLQGGDATALIGGTAVLILISVTLLAHRNQGLEKVTSYLIEGFVFGFKVFGPVIPIAAFFYLGDSAFTGLFGKVLPAGSHGIVNDLGVALADHVPLNGAVGAVTMTAIGAITGLDGSGFSGISLAGSIAQLFAAAIHSGAATLTALGQVAAIWVGGGTLIPWALIPAAAICGVSPFELARRNLKPVLLGLVATTIVAMFLV
>NZ_LN831776.1|WP_039787702.1|7654979_7655261_-|hypothetical-protein
MKHYESSLRTNSTVDQAQDAVTRLHNSVSQALSHPNDQTISQAENSLQHAEEAVSHAPEGSVGRHGVDLTEDRLAEEKQRLALAEAANGENKQ
>NZ_LN831776.1|WP_020426168.1|7653293_7654130_-|EcsC-family-protein
MTETAGAYPHLETAEELNAALAETTKWEKEQNKLMIWDHLTRLPFKVLDKLTPKFIHEKLGKLLDELGSYIQNGGNYLVAGRKVGSLMQAASRAAGGSGEGPFPLAVMDKAAEQLTQSSRNVATAQGATTGFGGVFTLAADIPAVLGLSLKVIQEIGLCYGYNPADKAERIFTVKVMQFASSDIVGKRTILKELNLQAGGNGDIAPGTNEAVSKIQGWKEVITVYRDNWGWKKMLQAIPVAGMFFGAYTNRKALEDVAEAARMLYRKRRIIARLAEME
>NZ_LN831776.1|WP_020426167.1|7652882_7653206_+|hypothetical-protein
MRKFGMYAKFTSKPGDREALAAILLEAAAAAETVKECELYIVNLSESEPDVLWVTEVWSNAEAHSASLKDEATRATIQRAMPLIAGVEPIPLVPLGGKGLAFGTMDA
>NZ_LN831776.1|WP_020426166.1|7652018_7652759_-|Bax-inhibitor-1/YccA-family-protein
MIGRSGNPTLNEKTFEREERYSGQERMSINGTVNKTFITLTILLAGAFSAWSMYFNGQDVSAYAIGGALAGFVLALIISFKPTAAPYLVPVYALAEGLFLGAISASYEGLYYGITLQAALLTLSIFVALLLAYKTRIIRATEKFKLGVFAATAGIAIVYLLSFVLGLFGVTVPYLHSNSLIGIGISVIIVIVAALNLVLDFDFIEHGAQQGAPKYMEWYGAFGLMVTLVWLYVEILRLLSKLRSRN
>NZ_LN831776.1|WP_020426204.1|7663164_7664022_-|SDR-family-oxidoreductase
MKIALTGATGHFGSIVAETLLKSVAAENLVVSVRNPEKADNLRTRGVDVRHGDFDQPETLDTAFAGVDRLLIVSADGDNDTRIRQHKAAVDAAVRAKVGFIVYTSVGHADSSSLFLAPVHRATEEFIRESGIPYSFLRNNWYLENEVGSIQAVQAGAPWVTSAGDGKVGWATRRDYAEAAAAVLAGEGHKNTVYELSGTPATQAELAAVVGKLLGKEVPVQQVDDAVYANIMAKAGVPEAALPIVVAIQQAIREGALDIASSDFTKLLQRPLTPLSEGVKDLLGN
>NZ_LN831776.1|WP_039785549.1|7664289_7665135_+|NAD(+)-diphosphatase
MSKPRASIYKRYIPAVTPPLEFSGSAYWLIFHSGRLLVTENAGITGIPFIPALEQISMTPLRTLYLGTFEGIACFAAQVQAETPEPEGMAFRPLRSLYESLDEDLFHLAGKGIQMLAWDETHQFCGRCGTATELVQTEHSRSCPACGLVSYPRIAPAVITAILKDNRILLAHSPHFVNNMYGLIAGFVEPGETLEDCVQRETMEEVGIKVKNIRYFASQQWPFPHSLMVGFLAEYESGEITVDGEELDHADWFELDRLPVIPSPVSIARKLIDWVVENRTN
>NZ_LN831776.1|WP_020426206.1|7665127_7665712_-|NAD(P)H-dependent-oxidoreductase
MNTLVIYTHPNHQSLNYAFLQEVLRGSRENAKVNEIQVLDLYEEGFNPVLVFNEHKRRRDMHSDPALAKYREQLLWADKIVLVYPIWWGRPPAMLMGYIDQMFASGFAYRDKGGLLPEGLLKGKSVVCISTMQGPTHYPLLMLHNAHKVLMRKVLFNFVGIRKVKFFEFGSMESKRGKHAQKLERIYRYFQTAN
>NZ_LN831776.1|WP_020426207.1|7665831_7666263_+|MarR-family-transcriptional-regulator
MDNELFQKFVAFTTAVHQITSDISKDIKPEALTPLQYKILEYIAVSQPVTLSEISDCMHMSMPNTSRELKKLSEKQLCDKITDPADRRKQGITLSPAGEAMMNEAFQHIAIRFTERIGDLTEEQRKEIERALDLLKEKVFYLR
>NZ_LN831776.1|WP_051010594.1|7666281_7667715_-|DHA2-family-efflux-MFS-transporter-permease-subunit
MEGNRMEKIPKGTILIMAILIIGSMVGLLNQSSLNTALPNIMGDFGLSTSTAQWLTTAFALVTGIVVPITAFLIQRFTTKQVFVFAMGMLTAGTLLCAVSPNFGLLLTGRMVQAVGVGIMLPLVQTLTFILIPVAKRGFTMGMIGLAINFAPAIGPVLNGWLVEDHSWRLLFYALFPCALLITIVGLFFVKNVTPQVKSKIDALSMTLSSLGFGGVLYGFSVSGSKGWGSTEVLISLVIGFIALGLFVWRQLTMENPLLEIRVFTSPAFTMATVISMILMIIMLSAQLLLPLYMQTMLGYSSLKSGLMLLPGAILICVMSPVAGKLFDKLGARMLVITGLSLTVVSTLLFTNLTENTSYAFLMIGYSLRMIGVSLTLLPVITSGMNSLAPDLIRHGIPVNTTLRTVAGSIGTALLVTIMTHSGGGLGQTSDVHGLIHGMNVASMVTAGSAVIALILAFFIKRKEAPVKSPANSIPVK
>NZ_LN831776.1|WP_081487086.1|7668230_7668905_-|TetR/AcrR-family-transcriptional-regulator
MIVSAEGKRSSKIYDAARTQGIILDAAEKIFAELGYSAARIDVIAKASGYNKSLIYQYFGDKLGLYTEVVKRADQIGEQITGSFIAELLKNEKLVTDPAAFKSFLEAMTREMVSFLLEHPSYLKILFWEAADDWKTWNQITYRPDDGTQLNDLAIAAKKSGILRQDLAPELFPILIMNVTTATLQYTSRYEHLLGKRDSPQLKERLIEQIAKFIIHGVMEPSLL
>NZ_LN831776.1|WP_020426211.1|7669098_7669440_-|alkylphosphonate-utilization-protein
MNELPNCPQCSSEYTYEDGMLLVCPECGHEWAQSAGNASSEESKVVRDANGNILNDGDSVTVIKDLKVKGSSSVLKIGTKVKNIRLVEGDHDIDCKIDGFGAMKLKSEFVRKA
>NZ_LN831776.1|WP_020426212.1|7669599_7670088_+|GNAT-family-N-acetyltransferase
MIILEAVPDPMSAESVELQAAILNSQPTFNLMVQHKEHLTPEEIREENKQNLEEMGEKMLLIVEKGKHIGIITYLPSHPGDKHCWIGLFVLHHGCAGRGIGSIALNALERRLRQENAAQVRLAVQLENLAGAAFWQKNGYVIVKSTQDQRGNEVDVYEKPLL
>NZ_LN831776.1|WP_020426213.1|7670095_7671310_-|chromate-transporter
METGSQRPVEAGGTKGKGAALLEVLGVSLKLGLTSFGGPIAHLGYFHNEYIRRRKWMDERSYADLVALCQFLPGPASSQVGIGIGVVRAGLLGGFIAWLGFTLPSVIALAVFALVLQGVDIAGAGWIHGLKIVAVAIVAQAVLGMGQKLTPDRGRVTIAVIAAVFALSWHAAYAQVLILAAAGVIGLWLYRGQPDRGPDLPIRISRTVAVSCLALFFLLLIALPLLRTSAGAGEFALFDSFYRSGSLVFGGGHVVLPLLEHEVVPAGWVSREDFLAGYGAAQAVPGPLFTFASYLGMMAAGFKGGIIATLGIFLPAFLLVIGALPFWNGLRSSPNVQGALAGINAAVVGILLAALYDPLWTSAILKPLDFALAAILFVMLFFWKLPPWVIVLAGAAGGMLIQLI
>NZ_LN831776.1|WP_082118159.1|7671538_7672423_-|Abi-family-protein
MEKFMIRISHSHKPSKTVEEQLQIFQSRGLIIEDEENAKEILSRISYYRFTAYTLSLKTNDKFYDNVTFNHIFRLYEFDLKFRLLLMELIEVVEVSMRTHISLVFAEKYDGMGYIDSANFYDSLKHADFINELEKLLKQSKDVFVKHYYDKYAGEFPIWVAIEVTTLGILSKLFKNLKKSDKNDIGMKFYSGLSGEFIASWLHAISNLRNICAHYGRIYNRNFPIAPKLFARDKKGIIDNNKVYAIVYNMKYLISDKKYWNSWVERLRSLIDEYSEVDLRLIGFHQNWYNLIKK

Crispr_ID: NZ_LN831776_79

• CRISPR_ID: NZ_LN831776_79
• CRISPR_location: 7713286-7713359
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_79

Consensus_repeat	Method
AAGTGGAAAAAGGATCACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_79

>79.1|7713309|28|NZ_LN831776|CRISPRCasFinder
TGCTCGAGCACCCTATTCTCCGCAGGTT

CRISPR arrays and Neighbor proteins around NZ_LN831776_79

CRISPR arrays

The CRISPR arrays of NZ_LN831776_79

>merge|NZ_LN831776|79|7713286-7713359|CRISPRCasFinder
AAGTGGAAAAAGGATCACTAATTTGCTCGAGCACCCTATTCTCCGCAGGTTAAGTGGAAAAAGGATCACTAATT

>NZ_LN831776|79|79|7713286-7713359|CRISPRCasFinder
AAGTGGAAAAAGGATCACTAATT	TGCTCGAGCACCCTATTCTCCGCAGGTT
AAGTGGAAAAAGGATCACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020434407.1|7707107_7707893_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|223377
NZ_LN831776.1|WP_046506129.1|7719744_7721652_+|transcription-antiterminator	unknown	unknown	gnl|CDD|226234
NZ_LN831776.1|WP_020434399.1|7712790_7713141_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|238045
NZ_LN831776.1|WP_046506122.1|7710281_7710872_+|chemotaxis-protein	unknown	unknown	gnl|CDD|369603
NZ_LN831776.1|WP_020434400.1|7712424_7712772_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|238045
NZ_LN831776.1|WP_020434409.1|7705257_7706004_-|nucleotidyltransferase-family-protein	unknown	unknown	gnl|CDD|133024
NZ_LN831776.1|WP_039791532.1|7706176_7706836_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_LN831776.1|WP_039791527.1|7713526_7715254_-|phosphoenolpyruvate--protein-phosphotransferase	unknown	unknown	gnl|CDD|224006
NZ_LN831776.1|WP_025708207.1|7721899_7722259_-|MerR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|133384
NZ_LN831776.1|WP_020434393.1|7718034_7719264_-|PTS-sugar-transporter-subunit-IIC	unknown	unknown	gnl|CDD|224372
NZ_LN831776.1|WP_020434392.1|7719278_7719605_-|PTS-sugar-transporter-subunit-IIB	unknown	unknown	gnl|CDD|99906
NZ_LN831776.1|WP_020434404.1|7709681_7710230_+|histidine-phosphatase-family-protein	unknown	unknown	gnl|CDD|223483
NZ_LN831776.1|WP_020434401.1|7711925_7712285_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|238045
NZ_LN831776.1|WP_020434406.1|7707905_7709039_+|SMP-30/gluconolactonase/LRE-family-protein	unknown	unknown	gnl|CDD|225921
NZ_LN831776.1|WP_085981704.1|7715556_7716192_-|membrane-protein	unknown	unknown	gnl|CDD|225239
NZ_LN831776.1|WP_020434388.1|7722357_7723068_+|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|187585
NZ_LN831776.1|WP_020434395.1|7716194_7717634_-|family-1-glycosylhydrolase	unknown	unknown	gnl|CDD|181973
NZ_LN831776.1|WP_020434405.1|7709161_7709533_-|RidA-family-protein	unknown	unknown	gnl|CDD|223329
NZ_LN831776.1|WP_020434394.1|7717666_7718014_-|PTS-lactose/cellobiose-transporter-subunit-IIA	unknown	unknown	gnl|CDD|376749
NZ_LN831776.1|WP_141639247.1|7715238_7715517_-|phosphocarrier-protein-HPr	unknown	unknown	gnl|CDD|237503

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020434407.1|7707107_7707893_+|SDR-family-oxidoreductase	gnl|CDD|223377	COG0300, DltE, Short-chain dehydrogenases of various substrate specificities [General function prediction only].	6.23062e-93
NZ_LN831776.1|WP_046506129.1|7719744_7721652_+|transcription-antiterminator	gnl|CDD|226234	COG3711, BglG, Transcriptional antiterminator [Transcription].	6.10743e-33
NZ_LN831776.1|WP_020434399.1|7712790_7713141_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	8.55945e-16
NZ_LN831776.1|WP_046506122.1|7710281_7710872_+|chemotaxis-protein	gnl|CDD|369603	pfam07931, CPT, Chloramphenicol phosphotransferase-like protein. The members of this family are all similar to chloramphenicol 3-O phosphotransferase (CPT) expressed by Streptomyces venezuelae. Chloramphenicol (Cm) is a metabolite produced by this bacterium that can inhibit ribosomal peptidyl transferase activity and therefore protein production. By transferring a phosphate group to the C-3 hydroxyl group of Cm, CPT inactivates this potentially lethal metabolite.	6.56673e-43
NZ_LN831776.1|WP_020434400.1|7712424_7712772_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	3.65368e-13
NZ_LN831776.1|WP_020434409.1|7705257_7706004_-|nucleotidyltransferase-family-protein	gnl|CDD|133024	cd04181, NTP_transferase, NTP_transferases catalyze the transfer of nucleotides onto phosphosugars. Nucleotidyltransferases transfer nucleotides onto phosphosugars. The enzyme family includes Alpha-D-Glucose-1-Phosphate Cytidylyltransferase, Mannose-1-phosphate guanyltransferase, and Glucose-1-phosphate thymidylyltransferase. The products are activated sugars that are precursors for synthesis of lipopolysaccharide, glycolipids and polysaccharides.	4.86169e-36
NZ_LN831776.1|WP_039791532.1|7706176_7706836_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.78549e-11
NZ_LN831776.1|WP_039791527.1|7713526_7715254_-|phosphoenolpyruvate--protein-phosphotransferase	gnl|CDD|224006	COG1080, PtsA, Phosphoenolpyruvate-protein kinase (PTS system EI component in bacteria) [Carbohydrate transport and metabolism].	0
NZ_LN831776.1|WP_025708207.1|7721899_7722259_-|MerR-family-transcriptional-regulator	gnl|CDD|133384	cd01109, HTH_YyaN, Helix-Turn-Helix DNA binding domain of the MerR-like transcription regulators YyaN and YraB. Putative helix-turn-helix (HTH) MerR-like transcription regulators of Bacillus subtilis, YyaN and YraB, and related proteins; N-terminal domain. Based on sequence similarity, these proteins are predicted to function as transcription regulators that mediate responses to stress in eubacteria. They belong to the MerR superfamily of transcription regulators that promote transcription of various stress regulons by reconfiguring the operator sequence located between the -35 and -10 promoter elements. A typical MerR regulator is comprised of distinct domains that harbor the regulatory (effector-binding) site and the active (DNA-binding) site. Their N-terminal domains are homologous and contain a DNA-binding winged HTH motif, while the C-terminal domains are often dissimilar and bind specific coactivator molecules such as metal ions, drugs, and organic substrates.	4.64698e-41
NZ_LN831776.1|WP_020434393.1|7718034_7719264_-|PTS-sugar-transporter-subunit-IIC	gnl|CDD|224372	COG1455, CelB, Phosphotransferase system cellobiose-specific component IIC [Carbohydrate transport and metabolism].	1.5003e-62
NZ_LN831776.1|WP_020434392.1|7719278_7719605_-|PTS-sugar-transporter-subunit-IIB	gnl|CDD|99906	cd05564, PTS_IIB_chitobiose_lichenan, PTS_IIB_chitobiose_lichenan: subunit IIB of enzyme II (EII) of the N,N-diacetylchitobiose-specific and lichenan-specific phosphoenolpyruvate:carbohydrate phosphotransferase system (PTS). In these systems, EII is either a lichenan- or an N,N-diacetylchitobiose-specific permease with two cytoplasmic domains (IIA and IIB) and a transmembrane channel IIC domain. In the chitobiose system, these subunits are expressed as separate proteins from chbA, chbB, and chbC of the chb operon (formerly the cel (cellulose) operon). In the lichenan system, these subunits are expressed from licA, licB, and licC of the lic operon. The lic operon of Bacillus subtilis is required for the transport and degradation of oligomeric beta-glucosides, which are produced by extracellular enzymes on substrates such as lichenan or barley glucan. The lic operon is transcribed from a gammaA-dependent promoter and is inducible by lichenan, lichenan hydrolysate, and cellobiose. The IIB domain fold includes a central four-stranded parallel open twisted beta-sheet flanked by alpha-helices on both sides. The seven major PTS systems with this IIB fold include chitobiose/lichenan, ascorbate, lactose, galactitol, mannitol, fructose, and a sensory system with similarity to the bacterial bgl system.	1.30074e-30
NZ_LN831776.1|WP_020434404.1|7709681_7710230_+|histidine-phosphatase-family-protein	gnl|CDD|223483	COG0406, phoE, Broad specificity phosphatase PhoE and related phosphatases [General function prediction only].	1.97038e-23
NZ_LN831776.1|WP_020434401.1|7711925_7712285_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	4.3084e-13
NZ_LN831776.1|WP_020434406.1|7707905_7709039_+|SMP-30/gluconolactonase/LRE-family-protein	gnl|CDD|225921	COG3386, COG3386, Gluconolactonase [Carbohydrate transport and metabolism].	1.54299e-29
NZ_LN831776.1|WP_085981704.1|7715556_7716192_-|membrane-protein	gnl|CDD|225239	COG2364, COG2364, Predicted membrane protein [Function unknown].	1.61573e-08
NZ_LN831776.1|WP_020434388.1|7722357_7723068_+|SDR-family-NAD(P)-dependent-oxidoreductase	gnl|CDD|187585	cd05324, carb_red_PTCR-like_SDR_c, Porcine testicular carbonyl reductase (PTCR)-like, classical (c) SDRs. PTCR is a classical SDR which catalyzes the NADPH-dependent reduction of ketones on steroids and prostaglandins. Unlike most SDRs, PTCR functions as a monomer. This subgroup also includes human carbonyl reductase 1 (CBR1) and CBR3. CBR1 is an NADPH-dependent SDR with broad substrate specificity and may be responsible for the in vivo reduction of quinones, prostaglandins, and other carbonyl-containing compounds. In addition it includes poppy NADPH-dependent salutaridine reductase which catalyzes the stereospecific reduction of salutaridine to 7(S)-salutaridinol in the biosynthesis of morphine, and Arabidopsis SDR1,a menthone reductase, which catalyzes the reduction of menthone to neomenthol, a compound with antimicrobial activity; SDR1 can also carry out neomenthol oxidation. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	6.19381e-67
NZ_LN831776.1|WP_020434395.1|7716194_7717634_-|family-1-glycosylhydrolase	gnl|CDD|181973	PRK09589, celA, 6-phospho-beta-glucosidase; Reviewed.	0
NZ_LN831776.1|WP_020434405.1|7709161_7709533_-|RidA-family-protein	gnl|CDD|223329	COG0251, TdcF, Putative translation initiation inhibitor, yjgF family [Translation, ribosomal structure and biogenesis].	1.00533e-20
NZ_LN831776.1|WP_020434394.1|7717666_7718014_-|PTS-lactose/cellobiose-transporter-subunit-IIA	gnl|CDD|376749	pfam02255, PTS_IIA, PTS system, Lactose/Cellobiose specific IIA subunit. The bacterial phosphoenolpyruvate: sugar phosphotransferase system (PTS) is a multi-protein system involved in the regulation of a variety of metabolic and transcriptional processes. The lactose/cellobiose-specific family are one of four structurally and functionally distinct group IIA PTS system enzymes. This family of proteins normally function as a homotrimer, stabilized by a centrally located metal ion. Separation into subunits is thought to occur after phosphorylation.	3.76411e-31
NZ_LN831776.1|WP_141639247.1|7715238_7715517_-|phosphocarrier-protein-HPr	gnl|CDD|237503	PRK13780, PRK13780, phosphocarrier protein HPr; Provisional.	8.45236e-43

Protein sequences

>NZ_LN831776.1|WP_020434399.1|7712790_7713141_+|helix-turn-helix-transcriptional-regulator
MNLPESVGNRIRELRKAKGWTQEQLAEAASLHYSYIGGVERGDRNISLETLAKIITAFQVPAVEIFRFEDETDRRKALDEHMTLISDRSTEEIAAITKINREVIATMGYGVGAKKH
>NZ_LN831776.1|WP_020434400.1|7712424_7712772_+|helix-turn-helix-transcriptional-regulator
MIDLRNTVGDRIRVIRKAKGLTQQQLAELSNLDDAYIGAVERGERNFSIDTLEKIVTALKIQPMELFQNHDDLNEVEAAQRRAIDEYAVTVSELSVKQINTLNRIVREVKGAFVD
>NZ_LN831776.1|WP_020434401.1|7711925_7712285_+|helix-turn-helix-transcriptional-regulator
MPDESKSELVKKIGERIRRLRKEMNLSQEQLAERSSLHTNYVGQVERGEKNLTLETLEKVVGGLDISLEELFRYIGPMEKQDALGQIVELLVERSVEDQNMALNVLKTVIEWEEKKIKE
>NZ_LN831776.1|WP_046506122.1|7710281_7710872_+|chemotaxis-protein
MKQGLIVLLNGTSSSGKTSISMELKNQKEIPFHHLSIDDFFGNYNDFIDNKYPDIEPTREVEDVGQILFDPIISVYYATIKLFSEMGLNVIVDTVIDNDKRFNDFLDLFFDHPTLFVGVLCSKEELTRREQIRGDREIGLANSQYDKIYSFTEYDLEVNTGELSPTECAEKILSFIKSDQDYSAFKKLSKREISVS
>NZ_LN831776.1|WP_020434404.1|7709681_7710230_+|histidine-phosphatase-family-protein
MTQFYLVRHGEPQWDINEHYKLKGHGRDLVPLTNKGINQVYLTAKDQRLKEAEIIVSSPYPRALQTAAILSKELGLEIMVEFDLREWQPDLTFEYDSLERLKELGDDYDANHGVYPPGINKLWETKELLKNRMEKVIDKYLEFQKVIITGHGMAFRTLVGEVGEIPHASIIEYYKKRHAALR
>NZ_LN831776.1|WP_020434405.1|7709161_7709533_-|RidA-family-protein
MDGIVRHDVNEEYAYSGFVEAGDFIFLSFCVGNVGGTVEEQVEGALDDMSSRLQQVGLGLADVVKLDILLRDVWDIPVMETVFKRRFQGKYPARKTISTEFAHVGGPDGLKVQMDGVAYRPRA
>NZ_LN831776.1|WP_020434406.1|7707905_7709039_+|SMP-30/gluconolactonase/LRE-family-protein
MSTEPKQRKRSTRQKVGRWSLALLGVIVLGIAVFLLIPAPVDPALWSAPAAPSFEKEGPWKENSKLSSAELVTDRAKFPEFITFDTKGRLYTGDSDGKIYRVAFDAEGKAQPAEVFADTHGTPNGLKFDAAGNLIVTDIQKGLLSIDPEGNIQVLTTEVEGGPIYLANELDIAQDGSIYFSDTSNYGKVMFKEIAENKPHGRLLKYDPQTKQTTVLLRDLYFANGVALSADEDFVLVAESYHYQLTRYWLKGAKQGTSDIFADNIAGFPDNITRDVHGHFWVGVFTTRLPFADYMHSHPWLAATMSKVPQSLLNGASAPVKHGLVAEYGPEGELVNSWHDPEGTLYGITTAVNQGGYLYLGTAPGGSQGVHRVLMNP
>NZ_LN831776.1|WP_020434407.1|7707107_7707893_+|SDR-family-oxidoreductase
MNIKGKWSLITGASSGIGEQFARQLAKEGSHLVLVARSKRKLDTLAAELTRSYGIQCQVVPQDLSIEGAAGELYQKCQQLNLNIDLLVNNAGFATHGLFEQISGERQHEEVMLNVAAVVDMTHLFLPGMLHRGAGAVINVSSTAGFQPLPYMAVYGATKAFVLSFTDALWWENRDRGVQFFALCPGSTETNFFNVVGTEDASVGAKDTPERVVEVTLRAMKKGKQYVVPGLRNYLGAQISRFMTRRQSLRLAQGMLSPRKQ
>NZ_LN831776.1|WP_039791532.1|7706176_7706836_-|TetR/AcrR-family-transcriptional-regulator
MSNEDKPSPSTGRVLKTYQEARLQNTENLRKLVVDAAAAILQEEGPEAVTVRRVSQKMGCSTKIIYSLFVNKEGLAQQLYLEGCKLLAQRFEEVPPSSDPLQHLLDLGEAFWQFGQEYTSYYKLMFGGAFAEFKPDAESMQGTMTAMSRLLILISTAQQQGQISDKEETQTIVSTIWASLHGVIHLYMGGFLGDADAAHTVYKQTIVLLSRSLFAVSKP
>NZ_LN831776.1|WP_020434409.1|7705257_7706004_-|nucleotidyltransferase-family-protein
MIALILAAGYATRLYPLTKDTPKPLLPVQGSRTILDLLLDRLEVLDEVAEVLIVTNDRFFRAFEQWSQKYRGTKPIRILNDGTTSPEGRLGAIGDIQFAIGREQIQDDLLVLAGDNVLGFGLEEYLSYFHQVDKDCILVRTVDDIRELRSVGVAELDAEMRVLSLEEKPQAPRTNIGVFALYIYKRSTLPLFSRYLAEGGNPDAPSYFPEWLHSRQEIRAYYTEGAIDDVGTPEAYAEMRARLGKLAE
>NZ_LN831776.1|WP_039791527.1|7713526_7715254_-|phosphoenolpyruvate--protein-phosphotransferase
MRNQLKGIGASSGIAIAKAYRLEEPELHILKKNVKDKEAEKQRLEQAISRSKAELEKITEYVNCELGADKAEILAAQLLVLNDPELLNPVFEKISTEGVNAEFALKESADRFVSMLESMDNEYMRERAKDIRDVTNRVTAHLLGVQISDPSLISEEVIIIAGDLTPSDTAQLNRRYVKGFTTDIGGRTSHSAIMARSMEIPAVVGTKQAVSMIENGIMVIVDGLEGEVIIDPSSEVIALYEAKKVKYEAQKALWAKVVHEPTVTKDGVHVELAANIGTPADVKGVLANGGEAVGLYRTEFLYMGKDRLPTEEEQFNAYKTVLEKMDGKPVVVRTLDIGGDKELPYLNLPKEMNPFLGFRAIRLCLEEQDIFRTQLRALLRAGSYGNLKIMFPMIATVSEFREAKAILMEEKEKLIASGVKAADNIEIGMMVEIPSTAVMADQFAKEVDFLSIGTNDLIQYTMAADRMNERVSYLYQPYNPAILRLVSMVIDAAHKEGKWVGMCGEMAGDPIAIPLLVSLGLDEFSMSATSILPARAQIKELSSEHATSVKEAVLSMKTSEEVIEYVKRTFDIHQV
>NZ_LN831776.1|WP_141639247.1|7715238_7715517_-|phosphocarrier-protein-HPr
MKKTFTVTDELGIHTRPASILVQAASKYNTEVNIEYNGRTVNLKSIVGVMSLGVPQGAQIQIAAAGSDADKAIEGIEEALKKEGLGEPCEIS
>NZ_LN831776.1|WP_085981704.1|7715556_7716192_-|membrane-protein
MRNFPALRKFGGRLLIVVVATALSALAVNLFIECNIGSDTLTVLLDGLHKSLGVSVGLASFCISIVFLAAGLLLNRTSIGFSSVMYSFLVGPLINWIHPFIANMNLADLSLFIKIVIVILANLCFSITYVLLMNFGNGMYAIDAVLRYMESKFGLRYAFGRIGADALFLSSGFLFGGIVGIGTVIAFALTGPGTVLLEKMLFKFRRIYKLR
>NZ_LN831776.1|WP_020434395.1|7716194_7717634_-|family-1-glycosylhydrolase
MKNIPTGFPSDFLWGGAVAANQLEGAYNVDGKGLSVADINEYMDGIPLDKKSNLELTTDYINEAIKSEDRIFPKRWGIDFYHTYKEDLKLLGELGLKTFRTSINWTRIFPNGDEAQPNEAGLKFYDDLIDEIIANGMEPMITLSHYEMPLHLTTAYKGWYSRELIDLFVRFGQVVFDRYHKKVKYWIIVNQINLIDHESFNHLGIAEDVVEDLASAKYQALHHEFVACGLITKYAKSLDSSLQIGMMLCGGPAYPATCRPEDIFATVRRNQMEYFFSDILLRGYYPGYAFRYFADNNITVEFAEGDEEALKNTADFMSFSYYYTRIYDAESMKNKTGPYRNTELPANPWGWTIDPIGLRTFLNLFYDRYQCPIYITENGIGYHDTLEEDGSIHDSYRVDYYRAHIEQMKEAIKDGVDLRGYYAWGPIDIISCSSSEMSKRYGFIYVDQDDRGNGSKKRLKKDSFSWMQKVIASNGENLD
>NZ_LN831776.1|WP_020434394.1|7717666_7718014_-|PTS-lactose/cellobiose-transporter-subunit-IIA
MTSEEVAQDAMQIILHAGEARKHCTDALKDIEKSDFAGAKEKMKLANAEIVIAHRVQTNCIQKETEGAKGEYSVLFAHAQDTLMTIYSEINIAKRLIDIFESFNQRLTQLEMINK
>NZ_LN831776.1|WP_020434393.1|7718034_7719264_-|PTS-sugar-transporter-subunit-IIC
MNKLIEWLKNDFSPKMNKVNNNVWVITLKDSVMQLLPFILLGSVFCLLTIPGDVYHIKNYPDFWVPFGWTMGMLSLLVSFLIPFNLMEKKKLRKQRFIAGCTSLITFLIIVTPQVVKDGTVGFKHSSLGTGGMFVAIIAALITGYIMSLFGKFSFFKEESVIPDFVRAWFDSMLPIGVTIILAWVLVDLVHIDIYNIILNIFMPLASVVETPWGFMLILFISCFLYSMGISSWILTPVTKPIFLAAIMANATAGAHNLVTAETIYSAYLWVGGVACTLPLAFMHLLSKSTKLKALGRASLVPSIFNINEPLVFGSIVWNPIMMLPMWINGLVLPLIVWIGTKVIHFGPIPKVVFDMWYVPFPISTWVTTGTITGIILMLIVVTAATLIWYPFFKAYEKQELEKELPQAN
>NZ_LN831776.1|WP_020434392.1|7719278_7719605_-|PTS-sugar-transporter-subunit-IIB
MANSSEMLHVLLVCGSGASSGFMAANIRKAAKKRNLNMDIIARGEAEIENYIDDIDALLVGPHLAYIVDEIEELTRDSDVKVLLMKPSYYSTLDGEAALNDLLSELKI
>NZ_LN831776.1|WP_046506129.1|7719744_7721652_+|transcription-antiterminator
MKTQYIDLIQYLSSQNNKWVSSQSLASKYDVSKRTIKSYISEINAIHHGLILSSNKGYKVDTHQVNRFLTSEQKAIPQTQPERMAYILKKLVQTNEPIYIYDLSDALFISESTLRLDLKLVKEKLTKNNLELQLIKDHVRLQGKEKDKRKLMSSILYEEANGSFIDIDKIKGVYKELNIDYIREVVIGTFSAHHFFTNDYYLTDVIIHITIALDRMKHDFQFLNKTLNYSMDNNAFLIAKEIASKLESYFHVTYPEEEIADLAILISCNGTNVNFTQIEVSDLENIAGIDCIDLVSEIAVDLDKYYYISIADSDFITRFTLHVKNLLMRLKNHHSTKNPLTNSIKRECPLIYDCAVHASHVIKERTGYTISDDEIAYLAFHLGYAIELQRQSNVKISCTVLFPLYYNMNVQIINKLQQYFGDDISIHSIVTDESDLSHATSDFIISSAQLHKIPEVPYVVITPFFIESDREKVSDKIFELKEQKKKNQFKINLESFLDERHFCSSTKRSDKEDVLRFICQIMNQDGYTDDDFFCKIMEREAMSSTAFGQVAIPHAIKMDSRKTGMFIYLNPNGIQWDTSTVKIVLLLTVSGEDRKIFRDVFDALATILTDDKNVNLLSSMHSFDDFINKLIACWE
>NZ_LN831776.1|WP_025708207.1|7721899_7722259_-|MerR-family-transcriptional-regulator
MFTIGQVAAKVGLNIGAIRFYERKGLLDPVVRNEQNNRLYTDDEINWLIFLRCLRETGMSVEEIKKYYDMVKAGTSTLPERIKLIQDQKQALLDDIDKKKAQLVHLEHKLERYYRGENY
>NZ_LN831776.1|WP_020434388.1|7722357_7723068_+|SDR-family-NAD(P)-dependent-oxidoreductase
MTKIALVTGANKGIGFEIARQLGEAGWKVLLGARSIERGKAAVAELTSQGLDVEFLQIDMTSLESIEQAAGTLRNNYPGLTLLINNAGMPGAFSSSFSNTQEEHLREAFEVNFFGTFRLNQRLLPLITENDGTIVNVSTDMASLHFMQNAEYALNAFDYNSSKTANNAMTVAMAIELKNSKAQVFAVTPGFTKTDLNGNAEGGKSKEAGAAIIVGYATDGKRHNGEFLDINGVYAW

Crispr_ID: NZ_LN831776_80

• CRISPR_ID: NZ_LN831776_80
• CRISPR_location: 7757527-7757600
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_LN831776_80

Consensus_repeat	Method
AAGTGGAAAAAGGATAACTAATT	CRISPRCasFinder

spacers of NZ_LN831776_80

>80.1|7757550|28|NZ_LN831776|CRISPRCasFinder
TGCTCGAACGCCCTGTTCTCCGCAGGTT

CRISPR arrays and Neighbor proteins around NZ_LN831776_80

CRISPR arrays

The CRISPR arrays of NZ_LN831776_80

>merge|NZ_LN831776|80|7757527-7757600|CRISPRCasFinder
AAGTGGAAAAAGGATAACTAATTTGCTCGAACGCCCTGTTCTCCGCAGGTTAAGTGGAAAAAGGATAACTAATT

>NZ_LN831776|80|80|7757527-7757600|CRISPRCasFinder
AAGTGGAAAAAGGATAACTAATT	TGCTCGAACGCCCTGTTCTCCGCAGGTT
AAGTGGAAAAAGGATAACTAATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_LN831776.1|WP_020434352.1|7757816_7758734_-|HPr-kinase/phosphorylase	unknown	unknown	gnl|CDD|235459
NZ_LN831776.1|WP_020434350.1|7760613_7761465_+|PRD-domain-containing-protein	unknown	unknown	gnl|CDD|170086
NZ_LN831776.1|WP_020434357.1|7752906_7753764_-|sugar-phosphate-isomerase/epimerase	unknown	unknown	gnl|CDD|224007
NZ_LN831776.1|WP_020434349.1|7761743_7763225_+|hypothetical-protein	unknown	unknown	gnl|CDD|367086
NZ_LN831776.1|WP_020434353.1|7756904_7757450_+|MerR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|237292
NZ_LN831776.1|WP_020434362.1|7748798_7750028_-|tetracycline-resistance-MFS-efflux-pump	unknown	unknown	gnl|CDD|340888
NZ_LN831776.1|WP_020434361.1|7750181_7750760_-|NAD(P)H-oxidoreductase	unknown	unknown	gnl|CDD|236620
NZ_LN831776.1|WP_020434347.1|7764870_7766394_-|malate:quinone-oxidoreductase	unknown	unknown	gnl|CDD|377591
NZ_LN831776.1|WP_020434348.1|7763229_7764792_+|glycoside-hydrolase-family-32-protein	unknown	unknown	gnl|CDD|224536
NZ_LN831776.1|WP_020434343.1|7770480_7773384_-|S-layer-homology-domain-containing-protein	unknown	unknown	gnl|CDD|306825
NZ_LN831776.1|WP_020434359.1|7751352_7751826_-|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_LN831776.1|WP_039791500.1|7753760_7754819_-|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_LN831776.1|WP_020434355.1|7754941_7755811_+|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225117
NZ_LN831776.1|WP_020434351.1|7759126_7760617_+|PTS-transporter-subunit-EIIC	unknown	unknown	gnl|CDD|131051
NZ_LN831776.1|WP_020434358.1|7751987_7752881_-|sugar-phosphate-isomerase/epimerase	unknown	unknown	gnl|CDD|224007
NZ_LN831776.1|WP_020434345.1|7768279_7769320_-|NTP-transferase-domain-containing-protein	unknown	unknown	gnl|CDD|133032
NZ_LN831776.1|WP_020434360.1|7750955_7751333_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224647
NZ_LN831776.1|WP_020434344.1|7769524_7770382_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_LN831776.1|WP_020434354.1|7755946_7756741_+|AIM24-family-protein	unknown	unknown	gnl|CDD|224924
NZ_LN831776.1|WP_020434346.1|7766812_7768159_-|hypothetical-protein	unknown	unknown	gnl|CDD|133037

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_LN831776.1|WP_020434352.1|7757816_7758734_-|HPr-kinase/phosphorylase	gnl|CDD|235459	PRK05428, PRK05428, HPr kinase/phosphorylase; Provisional.	1.45483e-141
NZ_LN831776.1|WP_020434350.1|7760613_7761465_+|PRD-domain-containing-protein	gnl|CDD|170086	PRK09772, PRK09772, transcriptional antiterminator BglG; Provisional.	5.97615e-43
NZ_LN831776.1|WP_020434357.1|7752906_7753764_-|sugar-phosphate-isomerase/epimerase	gnl|CDD|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	5.76335e-30
NZ_LN831776.1|WP_020434349.1|7761743_7763225_+|hypothetical-protein	gnl|CDD|367086	pfam02435, Glyco_hydro_68, Levansucrase/Invertase. This Pfam family consists of the glycosyl hydrolase 68 family, including several bacterial levansucrase enzymes, and invertase from zymomonas.	7.60214e-160
NZ_LN831776.1|WP_020434353.1|7756904_7757450_+|MerR-family-transcriptional-regulator	gnl|CDD|237292	PRK13182, racA, chromosome-anchoring protein RacA.	8.50301e-27
NZ_LN831776.1|WP_020434362.1|7748798_7750028_-|tetracycline-resistance-MFS-efflux-pump	gnl|CDD|340888	cd17330, MFS_SLC46_TetA_like, Eukaryotic Solute carrier 46 (SLC46) family, Bacterial Tetracycline resistance proteins, and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of the eukaryotic proteins MFSD9, MFSD10, MFSD14, and SLC46 family proteins, as well as bacterial multidrug resistance (MDR) transporters such as tetracycline resistance protein TetA and multidrug resistance protein MdtG. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. TetA proteins confer resistance to tetracycline while MdtG confers resistance to fosfomycin and deoxycholate. The Solute carrier 46 (SLC46) family is composed of three vertebrate members (SLC46A1, SLC46A2, and SLC46A3), the best-studied of which is SLC46A1, which functions both as an intestinal proton-coupled high-affinity folate transporter involved in the absorption of folates and as an intestinal heme transporter which mediates heme uptake. MFSD10 facilitates the uptake of organic anions such as some non-steroidal anti-inflammatory drugs (NSAIDs) and confers resistance to such NSAIDs. The SLC46/TetA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	3.02848e-89
NZ_LN831776.1|WP_020434361.1|7750181_7750760_-|NAD(P)H-oxidoreductase	gnl|CDD|236620	PRK09739, PRK09739, NAD(P)H oxidoreductase.	8.80712e-116
NZ_LN831776.1|WP_020434347.1|7764870_7766394_-|malate:quinone-oxidoreductase	gnl|CDD|377591	pfam06039, Mqo, Malate:quinone oxidoreductase (Mqo). This family consists of several bacterial Malate:quinone oxidoreductase (Mqo) proteins (EC:1.1.99.16). Mqo takes part in the citric acid cycle. It oxidizes L-malate to oxaloacetate and donates electrons to ubiquinone-1 and other artificial acceptors or, via the electron transfer chain, to oxygen. NAD is not an acceptor and the natural direct acceptor for the enzyme is most likely a quinone. The enzyme is therefore called malate:quinone oxidoreductase, abbreviated to Mqo. Mqo is a peripheral membrane protein and can be released from the membrane by addition of chelators.	0
NZ_LN831776.1|WP_020434348.1|7763229_7764792_+|glycoside-hydrolase-family-32-protein	gnl|CDD|224536	COG1621, SacC, Beta-fructosidases (levanase/invertase) [Carbohydrate transport and metabolism].	1.08712e-150
NZ_LN831776.1|WP_020434343.1|7770480_7773384_-|S-layer-homology-domain-containing-protein	gnl|CDD|306825	pfam00395, SLH, S-layer homology domain.	8.1686e-11
NZ_LN831776.1|WP_020434359.1|7751352_7751826_-|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	1.69296e-16
NZ_LN831776.1|WP_039791500.1|7753760_7754819_-|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	5.66689e-88
NZ_LN831776.1|WP_020434355.1|7754941_7755811_+|AraC-family-transcriptional-regulator	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	1.39075e-26
NZ_LN831776.1|WP_020434351.1|7759126_7760617_+|PTS-transporter-subunit-EIIC	gnl|CDD|131051	TIGR01996, Includes:_Phosphotransferase_enzyme_IIB_component, PTS system, sucrose-specific IIBC component. This model represents the fused enzyme II B and C components of the sucrose-specific PTS sugar transporter system. Sucrose is converted to sucrose-6-phosphate in the process of translocation into the cell. Some of these transporters lack their own IIA domains and instead use the glucose IIA protein (IIAglc or Crr). The exceptions to this rule are Staphylococci, Streptococci, Lactococci, Lactobacilli, etc. which contain their own A domain as a C-terminal fusion. This family is closely related to the trehalose transporting PTS IIBC enzymes and the B and C domains of each are described by subfamily-domain level TIGRFAMs models (TIGR00826 and TIGR00852, respectively).	5.48366e-131
NZ_LN831776.1|WP_020434358.1|7751987_7752881_-|sugar-phosphate-isomerase/epimerase	gnl|CDD|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	9.89349e-29
NZ_LN831776.1|WP_020434345.1|7768279_7769320_-|NTP-transferase-domain-containing-protein	gnl|CDD|133032	cd04189, G1P_TT_long, G1P_TT_long represents the long form of glucose-1-phosphate thymidylyltransferase. This family is the long form of Glucose-1-phosphate thymidylyltransferase. Glucose-1-phosphate thymidylyltransferase catalyses the formation of dTDP-glucose, from dTTP and glucose 1-phosphate. It is the first enzyme in the biosynthesis of dTDP-L-rhamnose, a cell wall constituent and a feedback inhibitor of the enzyme.There are two forms of Glucose-1-phosphate thymidylyltransferase in bacteria and archeae; short form and long form. The long form, which has an extra 50 amino acids c-terminal, is found in many species for which it serves as a sugar-activating enzyme for antibiotic biosynthesis and or other, unknown pathways, and in which dTDP-L-rhamnose is not necessarily produced.The long from enzymes also have a left-handed parallel helix domain at the c-terminus, whereas, th eshort form enzymes do not have this domain. The homotetrameric, feedback inhibited short form is found in numerous bacterial species that produce dTDP-L-rhamnose.	9.14916e-113
NZ_LN831776.1|WP_020434360.1|7750955_7751333_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	1.19293e-42
NZ_LN831776.1|WP_020434344.1|7769524_7770382_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	1.07597e-11
NZ_LN831776.1|WP_020434354.1|7755946_7756741_+|AIM24-family-protein	gnl|CDD|224924	COG2013, COG2013, Uncharacterized conserved protein [Function unknown].	2.2423e-45
NZ_LN831776.1|WP_020434346.1|7766812_7768159_-|hypothetical-protein	gnl|CDD|133037	cd04194, GT8_A4GalT_like, A4GalT_like proteins catalyze the addition of galactose or glucose residues to the lipooligosaccharide (LOS) or lipopolysaccharide (LPS) of the bacterial cell surface. The members of this family of glycosyltransferases catalyze the addition of galactose or glucose residues to the lipooligosaccharide (LOS) or lipopolysaccharide (LPS) of the bacterial cell surface. The enzymes exhibit broad substrate specificities. The known functions found in this family include: Alpha-1,4-galactosyltransferase, LOS-alpha-1,3-D-galactosyltransferase, UDP-glucose:(galactosyl) LPS alpha1,2-glucosyltransferase, UDP-galactose: (glucosyl) LPS alpha1,2-galactosyltransferase, and UDP-glucose:(glucosyl) LPS alpha1,2-glucosyltransferase. Alpha-1,4-galactosyltransferase from N. meningitidis adds an alpha-galactose from UDP-Gal (the donor) to a terminal lactose (the acceptor) of the LOS structure of outer membrane. LOSs are virulence factors that enable the organism to evade the immune system of host cells. In E. coli, the three alpha-1,2-glycosyltransferases, that are involved in the synthesis of the outer core region of the LPS, are all members of this family. The three enzymes share 40 % of sequence identity, but have different sugar donor or acceptor specificities, representing the structural diversity of LPS.	1.60306e-57

Protein sequences

>NZ_LN831776.1|WP_020434353.1|7756904_7757450_+|MerR-family-transcriptional-regulator
MEMLKTKDAAELLSVSQTTIKRWAAMFPDYFPKDRFGHYIFSEQEISLLKSIKERINHGEVLEYMNLGSAAGIQPPVSQQENPLHHTQDWPMGDMLSRIDYIERSLDHKADEVVSVQLLQQRAELEDLRQMIKQLAVSLETIQKPGAPSLSSHDELHPVAAKKLKTPPRKRGLLRNIFSCL
>NZ_LN831776.1|WP_020434354.1|7755946_7756741_+|AIM24-family-protein
MAYTINNLKDNSNVVIKEQLGGFTVIEYKEDLSTTTLAEAQSNFFMSKSNMRNKQLMIELNNSEVTLSAGAMQYMVGNIEMTSGVKGVGGLMRNIVSSAATGTSAIKPLYKGTGTILLETTYKYLWLIDVDNDHIVIDDGLFLACESSLQLAVTARKSLSSAALGGEGLFNLSAKGKGILALEAPIPSEEAVVIELQNDVLKVDGNFALMWSNTLDFTVEKSGKTRLGSAASGEGLVNVYRGTGTVWLAPLTSYRNSLFQANTP
>NZ_LN831776.1|WP_020434355.1|7754941_7755811_+|AraC-family-transcriptional-regulator
MLNYDKHLREPMDMPDPGFPIKVHTQRFDREGVVTFPHHWHEHLEFLFIESGEAVFECGRTPFSVRAGDLIAVNSNELHYGISASDDLLYYAIIADTALLHSAASDSAETKFIAPIRQNRLLFSNHVSGDQHISGCALTIIRELERREFGYELAVKAELYRLLALLLRRHGVTELSQAEQTRRIQTIERFAPVLRHIDTHYQEPIFVEGLAALAGLSRFHFSRLFKELTGHTVSEYVNAVRLDRADYMLRHTQLTVSEIAAATGFNDIYYFSRTFKKHKQRTPSSVRGF
>NZ_LN831776.1|WP_039791500.1|7753760_7754819_-|Gfo/Idh/MocA-family-oxidoreductase
MDMIRIGVIGTGSISGMHLNAYRNNPQTVVYAVCDLNEERARAAAAEYGAEKVYTDYRALLADSGVDAVSICTWNNSHAEISIAALKAGKHVLVEKPLCRTLEEAVQVQQAVEESGKILQVGFVRRYDANVQLLQKLAGAGEFGEIYYAKATTLRRLGNPGGWFSDIERSGGGPLIDIGVHVIDLCWYLMGRPKPVSVSANTYRKLGNRANVENLSFYKAADYDAANNTVEDLANALIRFENGASLLVDVSFTLHAKEDGRSVSLYGEKGGFEIDPETVIVSERANTIVNIYPQTDHKGFDFNSAFQNEIDHFTHCVQSGSQPLSPVQDGVAIMRILSGIYDSAAKGEEVKL
>NZ_LN831776.1|WP_020434357.1|7752906_7753764_-|sugar-phosphate-isomerase/epimerase
MKLGISTYSLHSAFAAGELTLKGVLETIADLGAEHAEIVPLGFNLIDNPELVGVILQTAADRGLELSNYAIGANFAGLEAAERRRELERVKREVDVCAALGIQRMRHDVASSPDLSIVRFLEELPQLAEACREIADYASGFGITTSVENHGYFIQHSDRVQALVNAVGRDNFRTTLDVGNFLCADENPLIAVASNLKLASMVHLKDFYIRPQDRHPGEGWFQSSGGNWLRGAIVGQGDIDMPRVLQLVKESGYDGYISIEFEGMEECRKGTRLGLEYVKRTWNAL
>NZ_LN831776.1|WP_020434358.1|7751987_7752881_-|sugar-phosphate-isomerase/epimerase
MARPVITNKIGVIVDSFQVGVKEGLRKAKEAGADGVQIYAVQGEFDPANLSPAARREWKDYIASMGLEISALVGDLGGHGFQDPAQNRAKIDKSKRIMELAKELGTDIVTTHIGIVPPNRDSQIYETMHTACEELSRYAHEMNAYFAIETGPETAAHLKMFLDGLGTKGVSVNFDPANMVMVTGDDPVQGVYALKDYIVHTHAKDGVKLAEIDPRNVYGQYGYEAPALDHEKVAEMAETGQAFREVPLGTGSVDWNGYLQALNDIGYKGYLTIEREVGSNPEADIRLAVEFLKGFRA
>NZ_LN831776.1|WP_020434359.1|7751352_7751826_-|MarR-family-transcriptional-regulator
MNKEEQVKMEFRDLFNKMAWLNKTKMEVSLKGYKPSEIHCIESIGRNVDSNVTKLAESLYMTRGAISKITKKLVEKGLIESYQKPDNKKEIYFRLTGQGEVINKIHEDLHKEFQERDKAVFEHVTEEQFDNMLSFMEKYSRHLDAEIKKQGIGIKSE
>NZ_LN831776.1|WP_020434360.1|7750955_7751333_+|helix-turn-helix-transcriptional-regulator
MTEHTKNNVQKKYQVGVEAALEVMGGKWKPLIIYHLMTGRKRTSELRRLMPGVTQKMLTTQLRGLEKDEIVTRKVYNEIPPRVEYELTHYGWGLKPALDHLCYWGEDHLEKIHGDKSKVLEEFRG
>NZ_LN831776.1|WP_020434361.1|7750181_7750760_-|NAD(P)H-oxidoreductase
MKVLSVVSHPRQDSLTFGVAGRFVQGLADAGHDYEILDLHRIGFDPVLQGADEPDLSAAQQSFSPEVEMEIRRMKEHDALAFIFPLWWWHLPAMLKGYIDRVWNNGFAYGSNHLHHQHVLWVALAGVSKDQMKKRNYDEMITHLLNVGIADYCGVPNSKVEFLYETLDSHPGHYEMLLNQAYHLGLNYAKDH
>NZ_LN831776.1|WP_020434362.1|7748798_7750028_-|tetracycline-resistance-MFS-efflux-pump
MFKFRSHKEQDTDQTIDKHALIFGLIAVFLCGIGFSIITPVVPFLVQPYISNPGEQAIVVTLLTSVYAVCVFFAAPVLGALSDKYGRRPLLLICLLGSAAGYFVFGVGGALWVLFAGRIIEGVTGGSISTIFAYFADIIPAEQRTKYFGWVSAVVGAGTVIGPTLGGLLARFGYAVPMYFGAIITLLNVVYGFFFMPESLDKNHRLKEIALVRLNPFTQLANILSMKSLQRLLVSAFLLWIPNGSLQAVFSQFTMDTFNWNPALIGLMFSIMGFQDILSQGLVMPKLLKKLSDQQIAVLGMVSEMIGYSLIALSALFSFYPLLIAGMFIFGFGDSVFGPSFNGMLSKSVDSSEQGRIQGGSQSIQALARMLGPILGGQIYVSLGHAAPAVMGMILIGAALPVLYKRTLP
>NZ_LN831776.1|WP_020434352.1|7757816_7758734_-|HPr-kinase/phosphorylase
MKSVTVQGLTEKFHLEVLAGASRMDREITRPRTHRPGLEFVGYFDFFPMERVQVLGRKEINYLLTLSVEERKLHIGNIVKYHPPCFIVTSGQQEIPYLTLFCNQEGIPLLRTGDTTTEFIAKLDSYLVKALAPELSIHGVCVNVSGIGILLRGKSGIGKSETAHTLIRRGHRFVADDIVVLKKLGPSTLLGTHNETTREFLALRSIGLINVVRQYGRKAFQDETRIVLDIELCPWRENSLNNELELVPQFTEYLGVQIPHIEVQLQPGRDVAGLIEAAANNWYLKQLGYSAAEEFMKRIEDGMQS
>NZ_LN831776.1|WP_020434351.1|7759126_7760617_+|PTS-transporter-subunit-EIIC
MPHDNIPIEQDGLTTKETRSPAGELAERLIGLSGGAGNVLEAIHCTTRLRLRLRDSSRVDEAGLSGIQEVQGVFFRTGQLQIILGSANVFKVHRQVVRILQEGGAKQQPEGTGDLSQKNRQEQQGVLKQIADAVSFFSDIVVPMIPLFVGVGLLLGLLSMMEVFGWAPRDSAAFRTLSLLTGSAFQMLAVMFGYHTAKRFGGTPPLGAVIGLVMTHPGLLHVTGFGRAPVSSADVMIAPQFGYQGAVIPTILAVLVMTLIEKGLRRMLPASASPMLIPFLSLASGGAIAILAIGPLTSELSASLGSMLELVFRSGGTVFGLLLGGIYSSLVVSGLHHGIQAIEIGLITNPDISVNFLLPIWSMANIAQGAAGLAVYARTRDPALRKIALPASITAFLGITEPVTFGVNLKLGRPFLGAAAGGAAGGAYVAFHQVAADSFGLTGIPMFAFTVQLGQLNVIHYAAGFLLAAATAFAVTWVLGVDEPSGDGTKKHRRIT
>NZ_LN831776.1|WP_020434350.1|7760613_7761465_+|PRD-domain-containing-protein
MKIKKILNNNAVVVNDLGEEKIVMGSGIAFQKRKNDIIDPSLVEKVFIMDDPDQYGHLQEMLGTLPEEEIAASEQIITYAEHELEVTFNEHIHIALTDHLSFALERIRKGTMIQNTLLDEIRILYPREFQIGLHAKSIIREALQVDIPVDEVGYIAMHIHTAWKNAGVRGSAAETAAMIRDLAEGVEQAAGITLERGSANYERLVTQLENILRTDENGKLLSELNPEIVRIAKERYTLAYVQATEISRLVEEDYSYVLSDSQRVCLAMEINRINTRSGNGNIS
>NZ_LN831776.1|WP_020434349.1|7761743_7763225_+|hypothetical-protein
MNIKKMARQAAAVTFATALLAGGGASALAKGNNNGDYKGNNSGDYKESYGFSHITREDMLKIPEQQKSGQFQVPAFNAASIQNISSAKGSDQWGNAIDLDVWDSWPLQNADGTVAEYNGYHIVFALAGDPKKGWDTFIYMFYQKVGDTSINSWKNAGRVFKDSDKYVPNDPILNKQAEEWSGSATLTKDGKVRLFYTNRQGWDPAHGFFGKQTLTTAQVNVSKPDADTLKVDGVEDFKSVFDGDGKFYQNVDQAFGGGDYADNHTLRDPHYVEDNGRKYLVFESNTGTETGYQGEESLYNRSFYEGSKVFFENEKNKLLSGPKKSLAALANGSLGIIELNDDYTLKSVMKPLIASNTVTDEIERANVFEMNGKWYLFTDSRGSKMTIDGIGANDVYMLGYVADSLTGPYKPLNGSGLVLHMNLDPNDLTWTYSHFAIPQAEGNNVVITSYMTNRGLYAEQHSTFAPSFLVNIKGSKTSVVKDSVLEQGQLTVK
>NZ_LN831776.1|WP_020434348.1|7763229_7764792_+|glycoside-hydrolase-family-32-protein
MNPKKRVWLQHSLLAAIGLGLIIAIGAAAYYSGRNNIPEEAAPSHSPPAYRAAYHFTTPDKWMNDPQRPVYLDGVYHYYYLYNRDYPAGNGTEWRHAVSVDLVHWTDEGIAIPKYTTPNGDPWSGSVVVDVTGSAGFGKGAVVAIMTQPSADGGQQEQYLWYSTDHGYTFRPYGHAPVLPNPGTADFRDPKIIWDDLSRKWVMVLAEGTKIGLYESKNLKAWHYMSGFVTEGIGIVECPDLYLMHAEDGAYKWVLGASANGIDSGKPNTYAYWTGDFDGVAFLPDRKEPQWLDYGFDWYGAVTFEDGTSRDATHHRYAMAWMNNWEYAQHTPTMREGFNGMDSIVRQIELKQAGGDSYRLVSEPLEALSQTAKEVATYERFDVKGSKTLPVTGDSYELNTDITWSELKNAGVRLRESADQSRHVDVGVFAEAGYTYVNRAYTGNPDKSGKYLESTAPFDVSKKKIHLKILVDRTSVEVFIDDGSVVYSNVVFPELDDKGITLFSDGGTAVFSNIVIKPLK
>NZ_LN831776.1|WP_020434347.1|7764870_7766394_-|malate:quinone-oxidoreductase
MSNRQKTDVILIGAGIMSATLGSLLKELVPDWKITVFERRAGAGEESSNEWNNAGTGHSSLCELNYTVEQPDGSIDISKAIKVNEEYQFSKQFWSYLVKSKRIQHPQDFIVPVPHMSFVQGEADVTFLKKRFEALSQNPLFQGMEFSEDPEQLMEWIPLMMKDRRINQPIAATRIESGTDVNFGALTRILFDHLQSNNTDIRYQHNVDDIKRAGDGSWDLKVRNLENGTTTRHSAKFVFIGGGGGSLHLLQKSGIPEGKGIGGFPVSGLFMVCQKPDIVAQHHAKVYGKAALGAPPMSVPHLDTRVIDKKESLFFGPFAGFSPKFLKYGSVFDLITSVKPGNLTTMLAAGAKNLSLTKYLIGQVMLSKDQRIEALREFVPGAQSGDWDLVVAGQRVQIIKDTAAGKGTLQFGTEVISSADGSIAALLGASPGASTAVSVMLEVIGKCFPQQLKAWEPKIKEMIPAYGVTLMENPKLINEIQKLTDRSLNLTSRAGEVEKKAPISSSS
>NZ_LN831776.1|WP_020434346.1|7766812_7768159_-|hypothetical-protein
MVELVLTINDKDGSYTEHAAVVLASIFSKTEQTINVHIVHDDSLSEENKVKLTQMVDVFHHNIFFYHVTIPGDMREVAAGVHKIDYWTMASMYRLLLPIIIQTDRVIYLDCDILVNMDINELWSIDLGDRYLGAVLDQGENLLEYFTSMGLSAELYFNSGVILFHLDNIRKKDNWYGEMLNFLRNFPKMTMPDQDVLNAVYSCNYLQLDQCFNTFAQNELDLEHKIIHFAGENKWWDADSPHVTLYNNFRAMTPWGWGGGYAPEPVIEAAFEPALADIPVEPPAPEVHFPEPPVQEFQFLPPPVQEAQFLAPPVQDIQLPAPPVQDIQLPAPPVQEIPVAEAPAPPPDNLPVKRHRRKIRRTLRLKRRLRRKRIIRARYRSIKRARLIKYRYVKRRILKLRRKKLRTVSRTGKLRTVSRRKHVIKRLSLRKSRHSLKRKHQRKLHKAG
>NZ_LN831776.1|WP_020434345.1|7768279_7769320_-|NTP-transferase-domain-containing-protein
MKGLILCAGRGTRLQPSTYTKPKCMLPVNGEYILVSIINKLVAAGITEIGIVVNHTQGEIRRTIGDGERWNASLTFLMQEEPMGLADAVKSAKSFMADSPFVLMLGDNLYEGDIAPLIRSLETDNAAASILLQQVKDPGQFGVAAVHAGQIIGLEEKPKYPKSDLAIVGVYALTAAIWPAMDRLTPSPRGEYEMTDAIQLLITEGGHVVYSIAAEPFFDIGTHDRWLEANRYKMGQDPQNFVKPSGMHSSVQWIPPVRIDPTATVMNSVVGPYVYIGPNSVVEDCILSNSILTDQVTLSHVHAEGSVFGSYVHLAEQEIQEQPARHILGDRASVTRTQAGLQNDSK
>NZ_LN831776.1|WP_020434344.1|7769524_7770382_+|GNAT-family-N-acetyltransferase
MSKNIVPLLYHSKEQIAGITRLEQDCSQSDSFYINAGIEHLAKAGGDHGILCYQDNQIIGLLSWYTADGSIANINAIVHPGHRRQGVFRSLLQRAAEDMKPQGIEALCFRVPQGSQAGLAAVQSLGAVFNRSEYLMTLKPMKINSPVSSDLSLFPARPEDFEFMVACSSAAFGDPEAWTRKYFTGTNEPGRATYVAWMNHYRVGLIRFNDLNGNTAIIHDFCILPTHQGKGLGQNVLILALELLLQKPYQQIRLSVVTDNERALNLYRNAGFEVKTEHQYYMSSL
>NZ_LN831776.1|WP_020434343.1|7770480_7773384_-|S-layer-homology-domain-containing-protein
MLFHAVRRKASLMIVFALLVSTLMPHMVFGEAAQFKDIAGSYAQKEIQSLAEAGIISGYEDNAFKPNKAMSRAELAKIIVLSLGLKVNGDQAAPFKDVDSKSWYRGYVGALVESGITEGTSATTFSPNSNVTREELVVFFIRAFGLEDTAKKLPVDSKLSDILEVSEWAKAQVSLAFKNGFINGVQGSDGTLKFKPKEHAERQALARLAYEFKTNKSVYVEKSKQLLAEEAAKGQNPVESPAATPAATQVTTDRGTSGGGSAPGTSAPATPTPAPTSPGPATPGPATPGPATPTPTPATPAPAPVSGLQIVVKGENTDAIYAEEPTEVIFRSSLNSAETVNASVYKVDDSGKVISQIISLYDDGSADHGDSLKADGIYSGKAVLTESTEGYINLQAFAGDVPSSTVFKLSVMKHLTDEQLAQTEIIENNTQAKLDHLATEYGDVQKAKEKTVAWLKAQDEVEHAGISGEGGSIWYLLDNGILGGISAAPENTKGLSSTIEEASSSNALAAEALTQNAEQTVATIGSKRVAVISPFSSKLTSSTVYDAVYNSFNQSNHSFLAERVKDTAANVNFFKRLNQYGVVVLDTHGDTFYDETVLQKLHNKYGIDFKYAGPQVMFLTGEKATAESKKAYELDLKKGRLAIVSGYYAITPSFITRYNDMLPGTIVYNGSCRSSYNDSMADAFINNGAGTYYGYTDYVKLAYDQAIAQSVSTALAGENMTTKEAFQAAVAAHGANDGLAAFAMKGSNIGVKTEGVINGTFENGNWTGWNGNGDVRVISKLGPLKPTEGNYMAIISTGLGFENNDNGGYDYNSDSYIEQSFIVPAGATTLSFDYNFISEEPKEYVGTKYNDTFKATVTSSVYINTASVITSHVNGGNTVTSNVYGDESVIIGTESINESTAYWIDENKVAIDFYGGDQTAYMTNWKHVQFDVSQFAGKASIVLRFHVWDQGDSVFDTAILIDNVILK

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	1226196-1226224	0	1.0
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	2395966-2395994	0	1.0
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	3277638-3277666	0	1.0
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	3901504-3901532	0	1.0
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	5044822-5044850	0	1.0
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	5056056-5056084	0	1.0
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	5725361-5725389	0	1.0
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	5738186-5738214	0	1.0
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	7889034-7889062	0	1.0
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	4235919-4235947	0	1.0
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	5995826-5995854	0	1.0
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	6455429-6455457	0	1.0
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	6926418-6926446	0	1.0
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	588012-588040	0	1.0
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	2920939-2920967	0	1.0
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	1226196-1226224	0	1.0
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	2395966-2395994	0	1.0
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	3277638-3277666	0	1.0
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	3901504-3901532	0	1.0
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	5044822-5044850	0	1.0
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	5056056-5056084	0	1.0
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	5725361-5725389	0	1.0
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	5738186-5738214	0	1.0
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	1226196-1226224	0	1.0
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	2395966-2395994	0	1.0
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	3277638-3277666	0	1.0
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	3901504-3901532	0	1.0
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	5044822-5044850	0	1.0
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	5056056-5056084	0	1.0
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	5725361-5725389	0	1.0
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	5738186-5738214	0	1.0
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	3476436-3476464	0	1.0
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	5526654-5526682	0	1.0
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	1226196-1226224	0	1.0
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	2395966-2395994	0	1.0
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	3277638-3277666	0	1.0
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	3901504-3901532	0	1.0
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	5044822-5044850	0	1.0
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	5056056-5056084	0	1.0
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	5725361-5725389	0	1.0
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	5738186-5738214	0	1.0
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	4235919-4235947	0	1.0
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	5995826-5995854	0	1.0
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	6455429-6455457	0	1.0
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	6926418-6926446	0	1.0
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	588012-588040	0	1.0
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	2920939-2920967	0	1.0
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	1226196-1226224	0	1.0
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	2395966-2395994	0	1.0
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	3277638-3277666	0	1.0
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	3901504-3901532	0	1.0
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	5044822-5044850	0	1.0
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	5056056-5056084	0	1.0
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	5725361-5725389	0	1.0
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	5738186-5738214	0	1.0
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	1226196-1226224	0	1.0
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	2395966-2395994	0	1.0
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	3277638-3277666	0	1.0
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	3901504-3901532	0	1.0
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	5044822-5044850	0	1.0
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	5056056-5056084	0	1.0
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	5725361-5725389	0	1.0
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	5738186-5738214	0	1.0
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	4235919-4235947	0	1.0
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	5995826-5995854	0	1.0
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	6455429-6455457	0	1.0
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	6926418-6926446	0	1.0
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	588012-588040	0	1.0
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	2920939-2920967	0	1.0
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	7889034-7889062	0	1.0
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	907334-907362	1	0.966
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	3346405-3346433	1	0.966
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	3476436-3476464	1	0.966
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	4605762-4605790	1	0.966
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	5526654-5526682	1	0.966
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	7889034-7889062	1	0.966
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	1226196-1226224	1	0.966
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	2395966-2395994	1	0.966
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	3277638-3277666	1	0.966
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	3901504-3901532	1	0.966
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	5044822-5044850	1	0.966
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	5056056-5056084	1	0.966
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	5725361-5725389	1	0.966
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	5738186-5738214	1	0.966
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	7177808-7177836	1	0.966
NZ_LN831776_12	12.1|819873|25|NZ_LN831776|CRISPRCasFinder	819873-819897	25	NZ_LN831776.1	114242-114266	1	0.96
NZ_LN831776_12	12.1|819873|25|NZ_LN831776|CRISPRCasFinder	819873-819897	25	NZ_LN831776.1	670770-670794	1	0.96
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	588012-588040	1	0.966
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	1226196-1226224	1	0.966
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	2395966-2395994	1	0.966
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	2920939-2920967	1	0.966
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	3277638-3277666	1	0.966
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	3901504-3901532	1	0.966
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	4235919-4235947	1	0.966
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	5044822-5044850	1	0.966
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	5056056-5056084	1	0.966
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	5725361-5725389	1	0.966
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	5738186-5738214	1	0.966
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	5995826-5995854	1	0.966
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	6455429-6455457	1	0.966
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	6926418-6926446	1	0.966
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	4681606-4681634	1	0.966
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	5526654-5526682	1	0.966
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	7889034-7889062	1	0.966
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	876663-876691	1	0.966
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	2484979-2485007	1	0.966
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	3476436-3476464	1	0.966
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	907334-907362	1	0.966
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	3346405-3346433	1	0.966
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	3476436-3476464	1	0.966
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	4605762-4605790	1	0.966
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	5526654-5526682	1	0.966
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	7889034-7889062	1	0.966
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	5526654-5526682	1	0.966
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	3476436-3476464	1	0.966
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	876663-876691	1	0.966
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	3476436-3476464	1	0.966
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	4054494-4054522	1	0.966
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	4681606-4681634	1	0.966
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	5526654-5526682	1	0.966
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	1226196-1226224	1	0.966
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	2395966-2395994	1	0.966
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	3277638-3277666	1	0.966
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	3901504-3901532	1	0.966
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	5044822-5044850	1	0.966
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	5056056-5056084	1	0.966
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	5725361-5725389	1	0.966
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	5738186-5738214	1	0.966
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	7177808-7177836	1	0.966
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	907334-907362	1	0.966
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	3346405-3346433	1	0.966
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	3476436-3476464	1	0.966
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	4605762-4605790	1	0.966
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	5526654-5526682	1	0.966
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	7889034-7889062	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	588012-588040	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	1226196-1226224	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	2395966-2395994	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	2920939-2920967	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	3277638-3277666	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	3901504-3901532	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	4054494-4054522	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	4235919-4235947	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	4390633-4390661	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	5004584-5004612	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	5044822-5044850	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	5056056-5056084	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	5725361-5725389	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	5738186-5738214	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	5995826-5995854	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	6455429-6455457	1	0.966
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	6926418-6926446	1	0.966
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	907334-907362	1	0.966
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	3346405-3346433	1	0.966
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	3476436-3476464	1	0.966
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	4605762-4605790	1	0.966
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	5526654-5526682	1	0.966
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	7889034-7889062	1	0.966
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	4681606-4681634	1	0.966
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	5526654-5526682	1	0.966
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	7889034-7889062	1	0.966
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	876663-876691	1	0.966
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	2484979-2485007	1	0.966
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	3476436-3476464	1	0.966
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	1226196-1226224	1	0.966
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	2395966-2395994	1	0.966
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	3277638-3277666	1	0.966
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	3901504-3901532	1	0.966
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	5044822-5044850	1	0.966
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	5056056-5056084	1	0.966
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	5725361-5725389	1	0.966
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	5738186-5738214	1	0.966
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	907334-907362	1	0.966
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	3346405-3346433	1	0.966
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	3476436-3476464	1	0.966
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	4605762-4605790	1	0.966
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	5526654-5526682	1	0.966
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	7889034-7889062	1	0.966
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	4605762-4605790	1	0.966
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	5044822-5044850	1	0.966
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	5056056-5056084	1	0.966
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	5725361-5725389	1	0.966
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	5738186-5738214	1	0.966
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	1226196-1226224	1	0.966
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	2395966-2395994	1	0.966
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	3277638-3277666	1	0.966
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	3901504-3901532	1	0.966
NZ_LN831776_58	58.1|5533299|29|NZ_LN831776|CRISPRCasFinder	5533299-5533327	29	NZ_LN831776.1	1226196-1226224	1	0.966
NZ_LN831776_58	58.1|5533299|29|NZ_LN831776|CRISPRCasFinder	5533299-5533327	29	NZ_LN831776.1	2395966-2395994	1	0.966
NZ_LN831776_58	58.1|5533299|29|NZ_LN831776|CRISPRCasFinder	5533299-5533327	29	NZ_LN831776.1	3277638-3277666	1	0.966
NZ_LN831776_58	58.1|5533299|29|NZ_LN831776|CRISPRCasFinder	5533299-5533327	29	NZ_LN831776.1	3901504-3901532	1	0.966
NZ_LN831776_58	58.1|5533299|29|NZ_LN831776|CRISPRCasFinder	5533299-5533327	29	NZ_LN831776.1	5044822-5044850	1	0.966
NZ_LN831776_58	58.1|5533299|29|NZ_LN831776|CRISPRCasFinder	5533299-5533327	29	NZ_LN831776.1	5056056-5056084	1	0.966
NZ_LN831776_58	58.1|5533299|29|NZ_LN831776|CRISPRCasFinder	5533299-5533327	29	NZ_LN831776.1	5725361-5725389	1	0.966
NZ_LN831776_58	58.1|5533299|29|NZ_LN831776|CRISPRCasFinder	5533299-5533327	29	NZ_LN831776.1	5738186-5738214	1	0.966
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	5526654-5526682	1	0.966
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	3476436-3476464	1	0.966
NZ_LN831776_63	63.1|6227005|29|NZ_LN831776|CRISPRCasFinder	6227005-6227033	29	NZ_LN831776.1	3865631-3865659	1	0.966
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	907334-907362	1	0.966
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	3346405-3346433	1	0.966
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	3476436-3476464	1	0.966
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	4605762-4605790	1	0.966
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	5526654-5526682	1	0.966
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	7889034-7889062	1	0.966
NZ_LN831776_69	69.1|6944723|28|NZ_LN831776|CRISPRCasFinder	6944723-6944750	28	NZ_LN831776.1	1558395-1558422	1	0.964
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	4681606-4681634	1	0.966
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	5526654-5526682	1	0.966
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	7889034-7889062	1	0.966
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	876663-876691	1	0.966
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	2484979-2485007	1	0.966
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	3476436-3476464	1	0.966
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	588012-588040	1	0.966
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	1226196-1226224	1	0.966
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	2395966-2395994	1	0.966
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	2920939-2920967	1	0.966
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	3277638-3277666	1	0.966
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	3901504-3901532	1	0.966
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	4235919-4235947	1	0.966
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	5044822-5044850	1	0.966
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	5056056-5056084	1	0.966
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	5725361-5725389	1	0.966
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	5738186-5738214	1	0.966
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	5995826-5995854	1	0.966
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	6455429-6455457	1	0.966
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	6926418-6926446	1	0.966
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	588012-588040	2	0.931
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	621745-621773	2	0.931
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	1989862-1989890	2	0.931
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	2920939-2920967	2	0.931
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	4054494-4054522	2	0.931
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	4235919-4235947	2	0.931
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	4390633-4390661	2	0.931
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	5004584-5004612	2	0.931
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	5144551-5144579	2	0.931
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	5995826-5995854	2	0.931
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	6455429-6455457	2	0.931
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	6926418-6926446	2	0.931
NZ_LN831776_2	2.1|134118|29|NZ_LN831776|CRISPRCasFinder	134118-134146	29	NZ_LN831776.1	7177808-7177836	2	0.931
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	907334-907362	2	0.931
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	3346405-3346433	2	0.931
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	3476436-3476464	2	0.931
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	4605762-4605790	2	0.931
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	5526654-5526682	2	0.931
NZ_LN831776_4	4.1|399030|29|NZ_LN831776|CRISPRCasFinder	399030-399058	29	NZ_LN831776.1	7889034-7889062	2	0.931
NZ_LN831776_12	12.1|819873|25|NZ_LN831776|CRISPRCasFinder	819873-819897	25	NZ_LN831776.1	7757660-7757684	2	0.92
NZ_LN831776_14	14.1|1028406|25|NZ_LN831776|CRISPRCasFinder	1028406-1028430	25	NZ_LN831776.1	7662920-7662944	2	0.92
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	876663-876691	2	0.931
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	907334-907362	2	0.931
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	2484979-2485007	2	0.931
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	3346405-3346433	2	0.931
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	3476436-3476464	2	0.931
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	4605762-4605790	2	0.931
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	4681606-4681634	2	0.931
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	4783417-4783445	2	0.931
NZ_LN831776_26	26.1|1861340|29|NZ_LN831776|CRISPRCasFinder	1861340-1861368	29	NZ_LN831776.1	5526654-5526682	2	0.931
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	4390633-4390661	2	0.931
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	5004584-5004612	2	0.931
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	5044822-5044850	2	0.931
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	5056056-5056084	2	0.931
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	5676769-5676797	2	0.931
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	5725361-5725389	2	0.931
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	5738186-5738214	2	0.931
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	1226196-1226224	2	0.931
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	2395966-2395994	2	0.931
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	3277638-3277666	2	0.931
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	3901504-3901532	2	0.931
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_LN831776.1	4054494-4054522	2	0.931
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	588012-588040	2	0.931
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	621745-621773	2	0.931
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	1989862-1989890	2	0.931
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	2920939-2920967	2	0.931
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	4054494-4054522	2	0.931
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	4235919-4235947	2	0.931
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	4390633-4390661	2	0.931
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	5004584-5004612	2	0.931
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	5144551-5144579	2	0.931
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	5995826-5995854	2	0.931
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	6455429-6455457	2	0.931
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	6926418-6926446	2	0.931
NZ_LN831776_28	28.1|2168776|29|NZ_LN831776|CRISPRCasFinder	2168776-2168804	29	NZ_LN831776.1	7177808-7177836	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	4235919-4235947	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	4390633-4390661	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	5004584-5004612	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	5044822-5044850	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	5056056-5056084	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	5725361-5725389	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	5738186-5738214	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	5995826-5995854	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	6455429-6455457	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	6926418-6926446	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	588012-588040	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	1226196-1226224	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	2395966-2395994	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	2920939-2920967	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	3277638-3277666	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	3901504-3901532	2	0.931
NZ_LN831776_29	29.1|2204246|29|NZ_LN831776|CRISPRCasFinder	2204246-2204274	29	NZ_LN831776.1	4054494-4054522	2	0.931
NZ_LN831776_32	32.1|2606679|27|NZ_LN831776|CRISPRCasFinder	2606679-2606705	27	NZ_LN831776.1	2820235-2820261	2	0.926
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	588012-588040	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	1226196-1226224	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	2395966-2395994	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	2920939-2920967	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	3277638-3277666	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	3901504-3901532	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	4235919-4235947	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	4390633-4390661	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	5004584-5004612	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	5044822-5044850	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	5056056-5056084	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	5725361-5725389	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	5738186-5738214	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	5995826-5995854	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	6455429-6455457	2	0.931
NZ_LN831776_35	35.1|2670880|29|NZ_LN831776|CRISPRCasFinder	2670880-2670908	29	NZ_LN831776.1	6926418-6926446	2	0.931
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	907334-907362	2	0.931
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	3346405-3346433	2	0.931
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	3476436-3476464	2	0.931
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	4605762-4605790	2	0.931
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	5526654-5526682	2	0.931
NZ_LN831776_36	36.1|2809443|29|NZ_LN831776|CRISPRCasFinder	2809443-2809471	29	NZ_LN831776.1	7889034-7889062	2	0.931
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	588012-588040	2	0.931
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	621745-621773	2	0.931
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	1989862-1989890	2	0.931
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	2920939-2920967	2	0.931
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	4054494-4054522	2	0.931
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	4235919-4235947	2	0.931
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	4390633-4390661	2	0.931
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	5004584-5004612	2	0.931
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	5144551-5144579	2	0.931
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	5995826-5995854	2	0.931
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	6455429-6455457	2	0.931
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	6926418-6926446	2	0.931
NZ_LN831776_38	38.1|3064886|29|NZ_LN831776|CRISPRCasFinder	3064886-3064914	29	NZ_LN831776.1	7177808-7177836	2	0.931
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	876663-876691	2	0.931
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	907334-907362	2	0.931
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	2484979-2485007	2	0.931
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	3346405-3346433	2	0.931
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	4605762-4605790	2	0.931
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	4681606-4681634	2	0.931
NZ_LN831776_39	39.1|3315110|29|NZ_LN831776|CRISPRCasFinder	3315110-3315138	29	NZ_LN831776.1	7889034-7889062	2	0.931
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	588012-588040	2	0.931
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	621745-621773	2	0.931
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	1989862-1989890	2	0.931
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	2920939-2920967	2	0.931
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	4054494-4054522	2	0.931
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	4235919-4235947	2	0.931
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	4390633-4390661	2	0.931
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	5004584-5004612	2	0.931
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	5144551-5144579	2	0.931
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	5995826-5995854	2	0.931
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	6455429-6455457	2	0.931
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	6926418-6926446	2	0.931
NZ_LN831776_41	41.1|3669468|29|NZ_LN831776|CRISPRCasFinder	3669468-3669496	29	NZ_LN831776.1	7177808-7177836	2	0.931
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	4390633-4390661	2	0.931
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	5004584-5004612	2	0.931
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	5044822-5044850	2	0.931
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	5056056-5056084	2	0.931
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	5676769-5676797	2	0.931
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	5725361-5725389	2	0.931
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	5738186-5738214	2	0.931
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	1226196-1226224	2	0.931
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	2395966-2395994	2	0.931
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	3277638-3277666	2	0.931
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	3901504-3901532	2	0.931
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_LN831776.1	4054494-4054522	2	0.931
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	907334-907362	2	0.931
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	2820582-2820610	2	0.931
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	3346405-3346433	2	0.931
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	3476436-3476464	2	0.931
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	4605762-4605790	2	0.931
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	5004584-5004612	2	0.931
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	5526654-5526682	2	0.931
NZ_LN831776_44	44.1|4559953|29|NZ_LN831776|CRISPRCasFinder	4559953-4559981	29	NZ_LN831776.1	7889034-7889062	2	0.931
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	588012-588040	2	0.931
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	621745-621773	2	0.931
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	1989862-1989890	2	0.931
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	2920939-2920967	2	0.931
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	4054494-4054522	2	0.931
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	4235919-4235947	2	0.931
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	4390633-4390661	2	0.931
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	5004584-5004612	2	0.931
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	5144551-5144579	2	0.931
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	5995826-5995854	2	0.931
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	6455429-6455457	2	0.931
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	6926418-6926446	2	0.931
NZ_LN831776_47	47.1|4775721|29|NZ_LN831776|CRISPRCasFinder	4775721-4775749	29	NZ_LN831776.1	7177808-7177836	2	0.931
NZ_LN831776_51	51.1|5084501|33|NZ_LN831776|CRISPRCasFinder	5084501-5084533	33	NZ_LN831776.1	70176-70208	2	0.939
NZ_LN831776_51	51.1|5084501|33|NZ_LN831776|CRISPRCasFinder	5084501-5084533	33	NZ_LN831776.1	6162071-6162103	2	0.939
NZ_LN831776_52	52.1|5129862|29|NZ_LN831776|CRISPRCasFinder	5129862-5129890	29	NZ_LN831776.1	1226196-1226224	2	0.931
NZ_LN831776_52	52.1|5129862|29|NZ_LN831776|CRISPRCasFinder	5129862-5129890	29	NZ_LN831776.1	2395966-2395994	2	0.931
NZ_LN831776_52	52.1|5129862|29|NZ_LN831776|CRISPRCasFinder	5129862-5129890	29	NZ_LN831776.1	3277638-3277666	2	0.931
NZ_LN831776_52	52.1|5129862|29|NZ_LN831776|CRISPRCasFinder	5129862-5129890	29	NZ_LN831776.1	3901504-3901532	2	0.931
NZ_LN831776_52	52.1|5129862|29|NZ_LN831776|CRISPRCasFinder	5129862-5129890	29	NZ_LN831776.1	5044822-5044850	2	0.931
NZ_LN831776_52	52.1|5129862|29|NZ_LN831776|CRISPRCasFinder	5129862-5129890	29	NZ_LN831776.1	5056056-5056084	2	0.931
NZ_LN831776_52	52.1|5129862|29|NZ_LN831776|CRISPRCasFinder	5129862-5129890	29	NZ_LN831776.1	5725361-5725389	2	0.931
NZ_LN831776_52	52.1|5129862|29|NZ_LN831776|CRISPRCasFinder	5129862-5129890	29	NZ_LN831776.1	5738186-5738214	2	0.931
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	5526654-5526682	2	0.931
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	7889034-7889062	2	0.931
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	907334-907362	2	0.931
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	1989862-1989890	2	0.931
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	3346405-3346433	2	0.931
NZ_LN831776_53	53.1|5294153|29|NZ_LN831776|CRISPRCasFinder	5294153-5294181	29	NZ_LN831776.1	3476436-3476464	2	0.931
NZ_LN831776_58	58.1|5533299|29|NZ_LN831776|CRISPRCasFinder	5533299-5533327	29	NZ_LN831776.1	907334-907362	2	0.931
NZ_LN831776_58	58.1|5533299|29|NZ_LN831776|CRISPRCasFinder	5533299-5533327	29	NZ_LN831776.1	3346405-3346433	2	0.931
NZ_LN831776_58	58.1|5533299|29|NZ_LN831776|CRISPRCasFinder	5533299-5533327	29	NZ_LN831776.1	3476436-3476464	2	0.931
NZ_LN831776_58	58.1|5533299|29|NZ_LN831776|CRISPRCasFinder	5533299-5533327	29	NZ_LN831776.1	4605762-4605790	2	0.931
NZ_LN831776_58	58.1|5533299|29|NZ_LN831776|CRISPRCasFinder	5533299-5533327	29	NZ_LN831776.1	5526654-5526682	2	0.931
NZ_LN831776_58	58.1|5533299|29|NZ_LN831776|CRISPRCasFinder	5533299-5533327	29	NZ_LN831776.1	7889034-7889062	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	4235919-4235947	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	4390633-4390661	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	5004584-5004612	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	5044822-5044850	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	5056056-5056084	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	5144551-5144579	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	5725361-5725389	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	5738186-5738214	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	5995826-5995854	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	6455429-6455457	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	6926418-6926446	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	588012-588040	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	1226196-1226224	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	2395966-2395994	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	2920939-2920967	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	3277638-3277666	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	3901504-3901532	2	0.931
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	NZ_LN831776.1	4054494-4054522	2	0.931
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	588012-588040	2	0.931
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	621745-621773	2	0.931
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	1989862-1989890	2	0.931
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	2920939-2920967	2	0.931
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	4054494-4054522	2	0.931
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	4235919-4235947	2	0.931
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	4390633-4390661	2	0.931
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	5004584-5004612	2	0.931
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	5144551-5144579	2	0.931
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	5995826-5995854	2	0.931
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	6455429-6455457	2	0.931
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	6926418-6926446	2	0.931
NZ_LN831776_68	68.1|6935571|29|NZ_LN831776|CRISPRCasFinder	6935571-6935599	29	NZ_LN831776.1	7177808-7177836	2	0.931
NZ_LN831776_69	69.1|6944723|28|NZ_LN831776|CRISPRCasFinder	6944723-6944750	28	NZ_LN831776.1	194911-194938	2	0.929
NZ_LN831776_69	69.1|6944723|28|NZ_LN831776|CRISPRCasFinder	6944723-6944750	28	NZ_LN831776.1	3157274-3157301	2	0.929
NZ_LN831776_69	69.1|6944723|28|NZ_LN831776|CRISPRCasFinder	6944723-6944750	28	NZ_LN831776.1	7713418-7713445	2	0.929
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	4390633-4390661	2	0.931
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	5004584-5004612	2	0.931
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	5044822-5044850	2	0.931
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	5056056-5056084	2	0.931
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	5676769-5676797	2	0.931
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	5725361-5725389	2	0.931
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	5738186-5738214	2	0.931
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	1226196-1226224	2	0.931
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	2395966-2395994	2	0.931
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	3277638-3277666	2	0.931
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	3901504-3901532	2	0.931
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_LN831776.1	4054494-4054522	2	0.931
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	876663-876691	2	0.931
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	907334-907362	2	0.931
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	2484979-2485007	2	0.931
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	3346405-3346433	2	0.931
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	3476436-3476464	2	0.931
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	4605762-4605790	2	0.931
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	4681606-4681634	2	0.931
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	4783417-4783445	2	0.931
NZ_LN831776_78	78.1|7662644|29|NZ_LN831776|CRISPRCasFinder	7662644-7662672	29	NZ_LN831776.1	5526654-5526682	2	0.931

1. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

2. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

3. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

4. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

5. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

6. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

7. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

8. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

9. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 0, identity: 1.0

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtacttcggca	Protospacer
*****************************

10. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 0, identity: 1.0

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*****************************

11. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 0, identity: 1.0

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*****************************

12. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 0, identity: 1.0

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*****************************

13. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 0, identity: 1.0

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*****************************

14. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 0, identity: 1.0

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*****************************

15. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 0, identity: 1.0

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*****************************

16. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

17. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

18. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

19. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

20. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

21. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

22. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

23. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

24. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

25. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

26. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

27. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

28. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

29. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

30. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

31. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

32. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 0, identity: 1.0

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*****************************

33. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 0, identity: 1.0

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*****************************

34. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

35. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

36. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

37. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

38. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

39. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

40. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

41. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 0, identity: 1.0

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****************************

42. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 0, identity: 1.0

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****************************

43. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 0, identity: 1.0

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****************************

44. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 0, identity: 1.0

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****************************

45. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 0, identity: 1.0

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****************************

46. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 0, identity: 1.0

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****************************

47. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 0, identity: 1.0

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****************************

48. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

49. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

50. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

51. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

52. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

53. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

54. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

55. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

56. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

57. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

58. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

59. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

60. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

61. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

62. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

63. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 0, identity: 1.0

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****************************

64. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 0, identity: 1.0

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****************************

65. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 0, identity: 1.0

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****************************

66. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 0, identity: 1.0

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****************************

67. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 0, identity: 1.0

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****************************

68. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 0, identity: 1.0

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****************************

69. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 0, identity: 1.0

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****************************

70. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 0, identity: 1.0

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctatcctcgggcagatg	Protospacer
*****************************

71. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 907334-907362, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catcagcccgaggatagggtactccggca	Protospacer
**** ************************

72. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 3346405-3346433, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
caactgcccgaggatagggtactccggca	Protospacer
** **************************

73. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*************.***************

74. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 4605762-4605790, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggttctccggca	Protospacer
******************** ********

75. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*************.***************

76. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtacttcggca	Protospacer
***********************.*****

77. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

78. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

79. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

80. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

81. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

82. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

83. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

84. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

85. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 7177808-7177836, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgctcgaggatagggtactctggca	Protospacer
************************.****

86. spacer 12.1|819873|25|NZ_LN831776|CRISPRCasFinder matches to position: 114242-114266, mismatch: 1, identity: 0.96

ctcagaaatcaacaattgtgaggtt	CRISPR spacer
ctcagaaatcaacaattgtgagatt	Protospacer
**********************.**

87. spacer 12.1|819873|25|NZ_LN831776|CRISPRCasFinder matches to position: 670770-670794, mismatch: 1, identity: 0.96

ctcagaaatcaacaattgtgaggtt	CRISPR spacer
ctcagaaatcaacaattgtgagatt	Protospacer
**********************.**

88. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 1, identity: 0.966

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.***************

89. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 1, identity: 0.966

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
***********************.*****

90. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 1, identity: 0.966

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
***********************.*****

91. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 1, identity: 0.966

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.***************

92. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 1, identity: 0.966

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
***********************.*****

93. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 1, identity: 0.966

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
***********************.*****

94. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 1, identity: 0.966

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.***************

95. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 1, identity: 0.966

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
***********************.*****

96. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 1, identity: 0.966

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
***********************.*****

97. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 1, identity: 0.966

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
***********************.*****

98. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 1, identity: 0.966

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
***********************.*****

99. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 1, identity: 0.966

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.***************

100. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 1, identity: 0.966

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.***************

101. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 1, identity: 0.966

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.***************

102. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 4681606-4681634, mismatch: 1, identity: 0.966

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctacccgagggtagggtacttcggca	Protospacer
*****.***********************

103. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 1, identity: 0.966

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
***********************.*****

104. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 1, identity: 0.966

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtacttcggca	Protospacer
*************.***************

105. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 876663-876691, mismatch: 1, identity: 0.966

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctacccgagggtagggtacttcggca	Protospacer
*****.***********************

106. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 2484979-2485007, mismatch: 1, identity: 0.966

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccaagggtagggtacttcggca	Protospacer
*********.*******************

107. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 1, identity: 0.966

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
***********************.*****

108. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 907334-907362, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catcagcccgaggatagggtactccggca	Protospacer
**** ************************

109. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 3346405-3346433, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
caactgcccgaggatagggtactccggca	Protospacer
** **************************

110. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*************.***************

111. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 4605762-4605790, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggttctccggca	Protospacer
******************** ********

112. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*************.***************

113. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtacttcggca	Protospacer
***********************.*****

114. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
************************* ***

115. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
************************* ***

116. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 876663-876691, mismatch: 1, identity: 0.966

catctacccgagggtagggtactccggca	CRISPR spacer
catctacccgagggtagggtacttcggca	Protospacer
***********************.*****

117. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 1, identity: 0.966

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*****.***********************

118. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 4054494-4054522, mismatch: 1, identity: 0.966

catctacccgagggtagggtactccggca	CRISPR spacer
catcttcccgagggtagggtactccggca	Protospacer
***** ***********************

119. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 4681606-4681634, mismatch: 1, identity: 0.966

catctacccgagggtagggtactccggca	CRISPR spacer
catctacccgagggtagggtacttcggca	Protospacer
***********************.*****

120. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 1, identity: 0.966

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*****.***********************

121. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

122. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

123. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

124. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

125. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

126. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

127. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

128. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*******.*********************

129. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 7177808-7177836, mismatch: 1, identity: 0.966

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgctcgaggatagggtactctggca	Protospacer
************************.****

130. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 907334-907362, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catcagcccgaggatagggtactccggca	Protospacer
**** ************************

131. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 3346405-3346433, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
caactgcccgaggatagggtactccggca	Protospacer
** **************************

132. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*************.***************

133. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 4605762-4605790, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggttctccggca	Protospacer
******************** ********

134. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*************.***************

135. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtacttcggca	Protospacer
***********************.*****

136. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
***********************.*****

137. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.***************

138. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.***************

139. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
***********************.*****

140. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.***************

141. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.***************

142. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 4054494-4054522, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catcttcccgagggtagggtactccggca	Protospacer
***** ***********************

143. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
***********************.*****

144. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 4390633-4390661, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcctgagggtagggtactccggca	Protospacer
********.********************

145. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 5004584-5004612, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtaatccggca	Protospacer
********************* *******

146. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.***************

147. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.***************

148. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.***************

149. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.***************

150. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
***********************.*****

151. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
***********************.*****

152. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 1, identity: 0.966

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
***********************.*****

153. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 907334-907362, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catcagcccgaggatagggtactccggca	Protospacer
**** ************************

154. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 3346405-3346433, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
caactgcccgaggatagggtactccggca	Protospacer
** **************************

155. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*************.***************

156. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 4605762-4605790, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggttctccggca	Protospacer
******************** ********

157. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*************.***************

158. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 1, identity: 0.966

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtacttcggca	Protospacer
***********************.*****

159. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 4681606-4681634, mismatch: 1, identity: 0.966

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggtagatg	Protospacer
***********************.*****

160. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 1, identity: 0.966

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
*****.***********************

161. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 1, identity: 0.966

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctatcctcgggcagatg	Protospacer
***************.*************

162. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 876663-876691, mismatch: 1, identity: 0.966

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggtagatg	Protospacer
***********************.*****

163. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 2484979-2485007, mismatch: 1, identity: 0.966

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctacccttgggcagatg	Protospacer
*******************.*********

164. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 1, identity: 0.966

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
*****.***********************

165. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 1, identity: 0.966

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*******.*********************

166. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 1, identity: 0.966

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*******.*********************

167. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 1, identity: 0.966

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*******.*********************

168. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 1, identity: 0.966

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*******.*********************

169. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 1, identity: 0.966

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*******.*********************

170. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 1, identity: 0.966

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*******.*********************

171. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 1, identity: 0.966

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*******.*********************

172. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 1, identity: 0.966

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*******.*********************

173. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 907334-907362, mismatch: 1, identity: 0.966

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggctgatg	Protospacer
************************ ****

174. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 3346405-3346433, mismatch: 1, identity: 0.966

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagttg	Protospacer
************************** **

175. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 1, identity: 0.966

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
***************.*************

176. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 4605762-4605790, mismatch: 1, identity: 0.966

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagaaccctatcctcgggcagatg	Protospacer
******** ********************

177. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 1, identity: 0.966

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
***************.*************

178. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 1, identity: 0.966

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctatcctcgggcagatg	Protospacer
*****.***********************

179. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 4605762-4605790, mismatch: 1, identity: 0.966

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccggagaaccctatcctcgggcagatg	Protospacer
********.********************

180. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 1, identity: 0.966

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
******** ********************

181. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 1, identity: 0.966

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
******** ********************

182. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 1, identity: 0.966

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
******** ********************

183. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 1, identity: 0.966

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
******** ********************

184. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 1, identity: 0.966

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
******** ********************

185. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 1, identity: 0.966

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
******** ********************

186. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 1, identity: 0.966

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
******** ********************

187. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 1, identity: 0.966

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
******** ********************

188. spacer 58.1|5533299|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 1, identity: 0.966

tgctggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
***.*************************

189. spacer 58.1|5533299|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 1, identity: 0.966

tgctggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
***.*************************

190. spacer 58.1|5533299|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 1, identity: 0.966

tgctggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
***.*************************

191. spacer 58.1|5533299|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 1, identity: 0.966

tgctggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
***.*************************

192. spacer 58.1|5533299|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 1, identity: 0.966

tgctggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
***.*************************

193. spacer 58.1|5533299|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 1, identity: 0.966

tgctggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
***.*************************

194. spacer 58.1|5533299|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 1, identity: 0.966

tgctggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
***.*************************

195. spacer 58.1|5533299|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 1, identity: 0.966

tgctggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
***.*************************

196. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 1, identity: 0.966

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
**************.**************

197. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 1, identity: 0.966

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
**************.**************

198. spacer 63.1|6227005|29|NZ_LN831776|CRISPRCasFinder matches to position: 3865631-3865659, mismatch: 1, identity: 0.966

tgccgaagtaccctaccctcgggcagata	CRISPR spacer
tgccgaagtaccctatcctcgggcagata	Protospacer
***************.*************

199. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 907334-907362, mismatch: 1, identity: 0.966

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggctgatg	Protospacer
************************ ****

200. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 3346405-3346433, mismatch: 1, identity: 0.966

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagttg	Protospacer
************************** **

201. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 1, identity: 0.966

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
***************.*************

202. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 4605762-4605790, mismatch: 1, identity: 0.966

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagaaccctatcctcgggcagatg	Protospacer
******** ********************

203. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 1, identity: 0.966

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
***************.*************

204. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 1, identity: 0.966

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctatcctcgggcagatg	Protospacer
*****.***********************

205. spacer 69.1|6944723|28|NZ_LN831776|CRISPRCasFinder matches to position: 1558395-1558422, mismatch: 1, identity: 0.964

aaacctcacaattgttgattttagggag	CRISPR spacer
aaacctcacaattgttgattttggggag	Protospacer
**********************.*****

206. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 4681606-4681634, mismatch: 1, identity: 0.966

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggtagatg	Protospacer
***********************.*****

207. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 1, identity: 0.966

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
*****.***********************

208. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 1, identity: 0.966

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctatcctcgggcagatg	Protospacer
***************.*************

209. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 876663-876691, mismatch: 1, identity: 0.966

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggtagatg	Protospacer
***********************.*****

210. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 2484979-2485007, mismatch: 1, identity: 0.966

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaagtaccctacccttgggcagatg	Protospacer
*******************.*********

211. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 1, identity: 0.966

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
*****.***********************

212. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 1, identity: 0.966

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
***************.*************

213. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 1, identity: 0.966

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.***********************

214. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 1, identity: 0.966

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.***********************

215. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 1, identity: 0.966

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
***************.*************

216. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 1, identity: 0.966

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.***********************

217. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 1, identity: 0.966

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.***********************

218. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 1, identity: 0.966

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
***************.*************

219. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 1, identity: 0.966

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.***********************

220. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 1, identity: 0.966

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.***********************

221. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 1, identity: 0.966

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.***********************

222. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 1, identity: 0.966

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.***********************

223. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 1, identity: 0.966

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
***************.*************

224. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 1, identity: 0.966

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
***************.*************

225. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 1, identity: 0.966

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
***************.*************

226. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

227. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 621745-621773, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccggggatagagtactccggca	Protospacer
**********.******.***********

228. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 1989862-1989890, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccggggatagggtgctccggca	Protospacer
**********.*********.********

229. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

230. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 4054494-4054522, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catcttcccgagggtagggtactccggca	Protospacer
***** *******.***************

231. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

232. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 4390633-4390661, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcctgagggtagggtactccggca	Protospacer
********.****.***************

233. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 5004584-5004612, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtaatccggca	Protospacer
*************.******* *******

234. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 5144551-5144579, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccaaggacagggtactccggca	Protospacer
*********.****.**************

235. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

236. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

237. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

238. spacer 2.1|134118|29|NZ_LN831776|CRISPRCasFinder matches to position: 7177808-7177836, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgctcgaggatagggtactctggca	Protospacer
*******.****************.****

239. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 907334-907362, mismatch: 2, identity: 0.931

catctgctcgaggatagggtactccggca	CRISPR spacer
catcagcccgaggatagggtactccggca	Protospacer
**** **.*********************

240. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 3346405-3346433, mismatch: 2, identity: 0.931

catctgctcgaggatagggtactccggca	CRISPR spacer
caactgcccgaggatagggtactccggca	Protospacer
** ****.*********************

241. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 2, identity: 0.931

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*******.*****.***************

242. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 4605762-4605790, mismatch: 2, identity: 0.931

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggttctccggca	Protospacer
*******.************ ********

243. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 2, identity: 0.931

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*******.*****.***************

244. spacer 4.1|399030|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 2, identity: 0.931

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtacttcggca	Protospacer
*******.***************.*****

245. spacer 12.1|819873|25|NZ_LN831776|CRISPRCasFinder matches to position: 7757660-7757684, mismatch: 2, identity: 0.92

ctcagaaatcaacaattgtgaggtt	CRISPR spacer
ctcggaaatcaacaattgtgagatt	Protospacer
***.******************.**

246. spacer 14.1|1028406|25|NZ_LN831776|CRISPRCasFinder matches to position: 7662920-7662944, mismatch: 2, identity: 0.92

gagcgctgaaggccggttcgcccgg	CRISPR spacer
gagcgctgaaggccagtttgcccgg	Protospacer
**************.***.******

247. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 876663-876691, mismatch: 2, identity: 0.931

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctacccgagggtagggtacttcggca	Protospacer
*****.*******.***************

248. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 907334-907362, mismatch: 2, identity: 0.931

catctgcccgaggatagggtacttcggca	CRISPR spacer
catcagcccgaggatagggtactccggca	Protospacer
**** ******************.*****

249. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 2484979-2485007, mismatch: 2, identity: 0.931

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccaagggtagggtacttcggca	Protospacer
*********.***.***************

250. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 3346405-3346433, mismatch: 2, identity: 0.931

catctgcccgaggatagggtacttcggca	CRISPR spacer
caactgcccgaggatagggtactccggca	Protospacer
** ********************.*****

251. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 2, identity: 0.931

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*************.*********.*****

252. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 4605762-4605790, mismatch: 2, identity: 0.931

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgaggatagggttctccggca	Protospacer
******************** **.*****

253. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 4681606-4681634, mismatch: 2, identity: 0.931

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctacccgagggtagggtacttcggca	Protospacer
*****.*******.***************

254. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 4783417-4783445, mismatch: 2, identity: 0.931

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgagaatagggaacttcggca	Protospacer
************.****** *********

255. spacer 26.1|1861340|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 2, identity: 0.931

catctgcccgaggatagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*************.*********.*****

256. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 4390633-4390661, mismatch: 2, identity: 0.931

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcctgagggtagggtactccggca	Protospacer
********.**************.*****

257. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 5004584-5004612, mismatch: 2, identity: 0.931

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgagggtagggtaatccggca	Protospacer
********************* *.*****

258. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 2, identity: 0.931

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********.*****

259. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 2, identity: 0.931

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********.*****

260. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 5676769-5676797, mismatch: 2, identity: 0.931

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccaagggtagggtatttcggca	Protospacer
*********.***********.*******

261. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 2, identity: 0.931

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********.*****

262. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 2, identity: 0.931

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********.*****

263. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 2, identity: 0.931

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********.*****

264. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 2, identity: 0.931

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********.*****

265. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 2, identity: 0.931

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********.*****

266. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 2, identity: 0.931

catctgcccgagggtagggtacttcggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********.*****

267. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to position: 4054494-4054522, mismatch: 2, identity: 0.931

catctgcccgagggtagggtacttcggca	CRISPR spacer
catcttcccgagggtagggtactccggca	Protospacer
***** *****************.*****

268. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

269. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 621745-621773, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccggggatagagtactccggca	Protospacer
**********.******.***********

270. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 1989862-1989890, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccggggatagggtgctccggca	Protospacer
**********.*********.********

271. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

272. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 4054494-4054522, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catcttcccgagggtagggtactccggca	Protospacer
***** *******.***************

273. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

274. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 4390633-4390661, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcctgagggtagggtactccggca	Protospacer
********.****.***************

275. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 5004584-5004612, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtaatccggca	Protospacer
*************.******* *******

276. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 5144551-5144579, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccaaggacagggtactccggca	Protospacer
*********.****.**************

277. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

278. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

279. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

280. spacer 28.1|2168776|29|NZ_LN831776|CRISPRCasFinder matches to position: 7177808-7177836, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgctcgaggatagggtactctggca	Protospacer
*******.****************.****

281. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
***********************.* ***

282. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 4390633-4390661, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcctgagggtagggtactccggca	Protospacer
********.**************** ***

283. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 5004584-5004612, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgagggtagggtaatccggca	Protospacer
********************* *** ***

284. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********** ***

285. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********** ***

286. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********** ***

287. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********** ***

288. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
***********************.* ***

289. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
***********************.* ***

290. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
***********************.* ***

291. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
***********************.* ***

292. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********** ***

293. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********** ***

294. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
***********************.* ***

295. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********** ***

296. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*************.*********** ***

297. spacer 29.1|2204246|29|NZ_LN831776|CRISPRCasFinder matches to position: 4054494-4054522, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactcccgca	CRISPR spacer
catcttcccgagggtagggtactccggca	Protospacer
***** ******************* ***

298. spacer 32.1|2606679|27|NZ_LN831776|CRISPRCasFinder matches to position: 2820235-2820261, mismatch: 2, identity: 0.926

gaagcgccgaaggctggtttgaccata	CRISPR spacer
gaagagccgaaggctggtttggccata	Protospacer
**** ****************.*****

299. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*****.*****************.*****

300. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****.*******.***************

301. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****.*******.***************

302. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*****.*****************.*****

303. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****.*******.***************

304. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****.*******.***************

305. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*****.*****************.*****

306. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 4390633-4390661, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcctgagggtagggtactccggca	Protospacer
*****.**.********************

307. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 5004584-5004612, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtaatccggca	Protospacer
*****.*************** *******

308. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****.*******.***************

309. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****.*******.***************

310. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****.*******.***************

311. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtactccggca	Protospacer
*****.*******.***************

312. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*****.*****************.*****

313. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*****.*****************.*****

314. spacer 35.1|2670880|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 2, identity: 0.931

catctacccgagggtagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*****.*****************.*****

315. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 907334-907362, mismatch: 2, identity: 0.931

catctgctcgaggatagggtactccggca	CRISPR spacer
catcagcccgaggatagggtactccggca	Protospacer
**** **.*********************

316. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 3346405-3346433, mismatch: 2, identity: 0.931

catctgctcgaggatagggtactccggca	CRISPR spacer
caactgcccgaggatagggtactccggca	Protospacer
** ****.*********************

317. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 2, identity: 0.931

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*******.*****.***************

318. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 4605762-4605790, mismatch: 2, identity: 0.931

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggttctccggca	Protospacer
*******.************ ********

319. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 2, identity: 0.931

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtactccggca	Protospacer
*******.*****.***************

320. spacer 36.1|2809443|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 2, identity: 0.931

catctgctcgaggatagggtactccggca	CRISPR spacer
catctgcccgaggatagggtacttcggca	Protospacer
*******.***************.*****

321. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

322. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 621745-621773, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccggggatagagtactccggca	Protospacer
**********.******.***********

323. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 1989862-1989890, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccggggatagggtgctccggca	Protospacer
**********.*********.********

324. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

325. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 4054494-4054522, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catcttcccgagggtagggtactccggca	Protospacer
***** *******.***************

326. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

327. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 4390633-4390661, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcctgagggtagggtactccggca	Protospacer
********.****.***************

328. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 5004584-5004612, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtaatccggca	Protospacer
*************.******* *******

329. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 5144551-5144579, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccaaggacagggtactccggca	Protospacer
*********.****.**************

330. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

331. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

332. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

333. spacer 38.1|3064886|29|NZ_LN831776|CRISPRCasFinder matches to position: 7177808-7177836, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgctcgaggatagggtactctggca	Protospacer
*******.****************.****

334. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 876663-876691, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactccggca	CRISPR spacer
catctacccgagggtagggtacttcggca	Protospacer
*****.*****************.*****

335. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 907334-907362, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactccggca	CRISPR spacer
catcagcccgaggatagggtactccggca	Protospacer
**** ********.***************

336. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 2484979-2485007, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccaagggtagggtacttcggca	Protospacer
*********.*************.*****

337. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 3346405-3346433, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactccggca	CRISPR spacer
caactgcccgaggatagggtactccggca	Protospacer
** **********.***************

338. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 4605762-4605790, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggttctccggca	Protospacer
*************.****** ********

339. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 4681606-4681634, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactccggca	CRISPR spacer
catctacccgagggtagggtacttcggca	Protospacer
*****.*****************.*****

340. spacer 39.1|3315110|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 2, identity: 0.931

catctgcccgagggtagggtactccggca	CRISPR spacer
catctgcccgaggatagggtacttcggca	Protospacer
*************.*********.*****

341. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

342. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 621745-621773, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccggggatagagtactccggca	Protospacer
**********.******.***********

343. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 1989862-1989890, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccggggatagggtgctccggca	Protospacer
**********.*********.********

344. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

345. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 4054494-4054522, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catcttcccgagggtagggtactccggca	Protospacer
***** *******.***************

346. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

347. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 4390633-4390661, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcctgagggtagggtactccggca	Protospacer
********.****.***************

348. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 5004584-5004612, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtaatccggca	Protospacer
*************.******* *******

349. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 5144551-5144579, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccaaggacagggtactccggca	Protospacer
*********.****.**************

350. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

351. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

352. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgcccgagggtagggtacttcggca	Protospacer
*************.*********.*****

353. spacer 41.1|3669468|29|NZ_LN831776|CRISPRCasFinder matches to position: 7177808-7177836, mismatch: 2, identity: 0.931

catctgcccgaggatagggtactccggca	CRISPR spacer
catctgctcgaggatagggtactctggca	Protospacer
*******.****************.****

354. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 4390633-4390661, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcaggcagatg	Protospacer
*****.**************.********

355. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 5004584-5004612, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggattaccctaccctcgggcagatg	Protospacer
*****.* *********************

356. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

357. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

358. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 5676769-5676797, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaaataccctacccttgggcagatg	Protospacer
*******.***********.*********

359. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

360. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

361. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

362. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

363. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

364. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

365. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to position: 4054494-4054522, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggaagatg	Protospacer
*****.***************** *****

366. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 907334-907362, mismatch: 2, identity: 0.931

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggctgatg	Protospacer
*******.**************** ****

367. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 2820582-2820610, mismatch: 2, identity: 0.931

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggaataccttatcctcgtgcagatg	Protospacer
************.******** *******

368. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 3346405-3346433, mismatch: 2, identity: 0.931

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagttg	Protospacer
*******.****************** **

369. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 2, identity: 0.931

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
*******.*******.*************

370. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 4605762-4605790, mismatch: 2, identity: 0.931

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggagaaccctatcctcgggcagatg	Protospacer
*******. ********************

371. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 5004584-5004612, mismatch: 2, identity: 0.931

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggattaccctaccctcgggcagatg	Protospacer
******* *******.*************

372. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 2, identity: 0.931

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
*******.*******.*************

373. spacer 44.1|4559953|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 2, identity: 0.931

tgccggaataccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctatcctcgggcagatg	Protospacer
*****.*.*********************

374. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.*********.*************

375. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 621745-621773, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtactctatccccgggcagatg	Protospacer
***********.******.**********

376. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 1989862-1989890, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagcaccctatccccgggcagatg	Protospacer
********.*********.**********

377. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.*********.*************

378. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 4054494-4054522, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggaagatg	Protospacer
***************.******* *****

379. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.*********.*************

380. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 4390633-4390661, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcaggcagatg	Protospacer
***************.****.********

381. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 5004584-5004612, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggattaccctaccctcgggcagatg	Protospacer
******* *******.*************

382. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 5144551-5144579, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctgtccttgggcagatg	Protospacer
**************.****.*********

383. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.*********.*************

384. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.*********.*************

385. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.*********.*************

386. spacer 47.1|4775721|29|NZ_LN831776|CRISPRCasFinder matches to position: 7177808-7177836, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccagagtaccctatcctcgagcagatg	Protospacer
****.****************.*******

387. spacer 51.1|5084501|33|NZ_LN831776|CRISPRCasFinder matches to position: 70176-70208, mismatch: 2, identity: 0.939

ttcgtacaaaactggcttcggaagcatacgctt	CRISPR spacer
ttcgtacaaaacttgcttcggaagcatccgctt	Protospacer
************* ************* *****

388. spacer 51.1|5084501|33|NZ_LN831776|CRISPRCasFinder matches to position: 6162071-6162103, mismatch: 2, identity: 0.939

ttcgtacaaaactggcttcggaagcatacgctt	CRISPR spacer
ttcgtacaaaactagcttcgaaagcatacgctt	Protospacer
*************.******.************

389. spacer 52.1|5129862|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 2, identity: 0.931

tgccggagtaacctatcttcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
********** ******.***********

390. spacer 52.1|5129862|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 2, identity: 0.931

tgccggagtaacctatcttcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
********** ******.***********

391. spacer 52.1|5129862|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 2, identity: 0.931

tgccggagtaacctatcttcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
********** ******.***********

392. spacer 52.1|5129862|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 2, identity: 0.931

tgccggagtaacctatcttcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
********** ******.***********

393. spacer 52.1|5129862|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 2, identity: 0.931

tgccggagtaacctatcttcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
********** ******.***********

394. spacer 52.1|5129862|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 2, identity: 0.931

tgccggagtaacctatcttcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
********** ******.***********

395. spacer 52.1|5129862|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 2, identity: 0.931

tgccggagtaacctatcttcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
********** ******.***********

396. spacer 52.1|5129862|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 2, identity: 0.931

tgccggagtaacctatcttcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
********** ******.***********

397. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 2, identity: 0.931

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
******** ******.*************

398. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 2, identity: 0.931

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctatcctcgggcagatg	Protospacer
*****.** ********************

399. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 907334-907362, mismatch: 2, identity: 0.931

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggctgatg	Protospacer
******** *************** ****

400. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 1989862-1989890, mismatch: 2, identity: 0.931

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccggagcaccctatccccgggcagatg	Protospacer
******** *********.**********

401. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 3346405-3346433, mismatch: 2, identity: 0.931

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagttg	Protospacer
******** ***************** **

402. spacer 53.1|5294153|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 2, identity: 0.931

tgccggaggaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
******** ******.*************

403. spacer 58.1|5533299|29|NZ_LN831776|CRISPRCasFinder matches to position: 907334-907362, mismatch: 2, identity: 0.931

tgctggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggctgatg	Protospacer
***.******************** ****

404. spacer 58.1|5533299|29|NZ_LN831776|CRISPRCasFinder matches to position: 3346405-3346433, mismatch: 2, identity: 0.931

tgctggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagttg	Protospacer
***.********************** **

405. spacer 58.1|5533299|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 2, identity: 0.931

tgctggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
***.***********.*************

406. spacer 58.1|5533299|29|NZ_LN831776|CRISPRCasFinder matches to position: 4605762-4605790, mismatch: 2, identity: 0.931

tgctggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagaaccctatcctcgggcagatg	Protospacer
***.**** ********************

407. spacer 58.1|5533299|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 2, identity: 0.931

tgctggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
***.***********.*************

408. spacer 58.1|5533299|29|NZ_LN831776|CRISPRCasFinder matches to position: 7889034-7889062, mismatch: 2, identity: 0.931

tgctggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctatcctcgggcagatg	Protospacer
***.*.***********************

409. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.********.**************

410. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 4390633-4390661, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcaggcagatg	Protospacer
**************.*****.********

411. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 5004584-5004612, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccggattaccctaccctcgggcagatg	Protospacer
******* ******.**************

412. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
**************..*************

413. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
**************..*************

414. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 5144551-5144579, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccggagtaccctgtccttgggcagatg	Protospacer
***************.***.*********

415. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
**************..*************

416. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
**************..*************

417. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.********.**************

418. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.********.**************

419. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.********.**************

420. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.********.**************

421. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
**************..*************

422. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
**************..*************

423. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.********.**************

424. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
**************..*************

425. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
**************..*************

426. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to position: 4054494-4054522, mismatch: 2, identity: 0.931

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggaagatg	Protospacer
**************.******** *****

427. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 588012-588040, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.*********.*************

428. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 621745-621773, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtactctatccccgggcagatg	Protospacer
***********.******.**********

429. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 1989862-1989890, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagcaccctatccccgggcagatg	Protospacer
********.*********.**********

430. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 2920939-2920967, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.*********.*************

431. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 4054494-4054522, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggaagatg	Protospacer
***************.******* *****

432. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 4235919-4235947, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.*********.*************

433. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 4390633-4390661, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcaggcagatg	Protospacer
***************.****.********

434. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 5004584-5004612, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggattaccctaccctcgggcagatg	Protospacer
******* *******.*************

435. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 5144551-5144579, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctgtccttgggcagatg	Protospacer
**************.****.*********

436. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 5995826-5995854, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.*********.*************

437. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 6455429-6455457, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.*********.*************

438. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 6926418-6926446, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggcagatg	Protospacer
*****.*********.*************

439. spacer 68.1|6935571|29|NZ_LN831776|CRISPRCasFinder matches to position: 7177808-7177836, mismatch: 2, identity: 0.931

tgccggagtaccctatcctcgggcagatg	CRISPR spacer
tgccagagtaccctatcctcgagcagatg	Protospacer
****.****************.*******

440. spacer 69.1|6944723|28|NZ_LN831776|CRISPRCasFinder matches to position: 194911-194938, mismatch: 2, identity: 0.929

aaacctcacaattgttgattttagggag	CRISPR spacer
aaacctcacaattgttgattctggggag	Protospacer
********************.*.*****

441. spacer 69.1|6944723|28|NZ_LN831776|CRISPRCasFinder matches to position: 3157274-3157301, mismatch: 2, identity: 0.929

aaacctcacaattgttgattttagggag	CRISPR spacer
aaatctcacaattgttgattttggggag	Protospacer
***.******************.*****

442. spacer 69.1|6944723|28|NZ_LN831776|CRISPRCasFinder matches to position: 7713418-7713445, mismatch: 2, identity: 0.929

aaacctcacaattgttgattttagggag	CRISPR spacer
aaatctcacaattgttgattttggggag	Protospacer
***.******************.*****

443. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 4390633-4390661, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcaggcagatg	Protospacer
*****.**************.********

444. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 5004584-5004612, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggattaccctaccctcgggcagatg	Protospacer
*****.* *********************

445. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 5044822-5044850, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

446. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 5056056-5056084, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

447. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 5676769-5676797, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccgaaataccctacccttgggcagatg	Protospacer
*******.***********.*********

448. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 5725361-5725389, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

449. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 5738186-5738214, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

450. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 1226196-1226224, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

451. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 2395966-2395994, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

452. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 3277638-3277666, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

453. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 3901504-3901532, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagatg	Protospacer
*****.*********.*************

454. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to position: 4054494-4054522, mismatch: 2, identity: 0.931

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggaagatg	Protospacer
*****.***************** *****

455. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 876663-876691, mismatch: 2, identity: 0.931

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggtagatg	Protospacer
***************.*******.*****

456. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 907334-907362, mismatch: 2, identity: 0.931

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggctgatg	Protospacer
*****.****************** ****

457. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 2484979-2485007, mismatch: 2, identity: 0.931

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctacccttgggcagatg	Protospacer
***************.***.*********

458. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 3346405-3346433, mismatch: 2, identity: 0.931

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctatcctcgggcagttg	Protospacer
*****.******************** **

459. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 3476436-3476464, mismatch: 2, identity: 0.931

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
*****.*********.*************

460. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 4605762-4605790, mismatch: 2, identity: 0.931

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagaaccctatcctcgggcagatg	Protospacer
*****.** ********************

461. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 4681606-4681634, mismatch: 2, identity: 0.931

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagtaccctaccctcgggtagatg	Protospacer
***************.*******.*****

462. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 4783417-4783445, mismatch: 2, identity: 0.931

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccgaagttccctattctcgggcagatg	Protospacer
********* ******.************

463. spacer 78.1|7662644|29|NZ_LN831776|CRISPRCasFinder matches to position: 5526654-5526682, mismatch: 2, identity: 0.931

tgccgaagtaccctatcctcgggcagatg	CRISPR spacer
tgccggagtaccctaccctcgggcagatg	Protospacer
*****.*********.*************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_LN831776_17	17.1|1269276|25|NZ_LN831776|CRISPRCasFinder	1269276-1269300	25	NC_009507	Sphingomonas wittichii RW1 plasmid pSWIT01, complete sequence	13373-13397	3	0.88
NZ_LN831776_14	14.1|1028406|25|NZ_LN831776|CRISPRCasFinder	1028406-1028430	25	NZ_CP029833	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed3, complete sequence	271993-272017	4	0.84
NZ_LN831776_14	14.1|1028406|25|NZ_LN831776|CRISPRCasFinder	1028406-1028430	25	KY940711	Bradyrhizobium phage BDU-MI-1, complete genome	81082-81106	4	0.84
NZ_LN831776_17	17.2|1269328|25|NZ_LN831776|CRISPRCasFinder	1269328-1269352	25	MN792917	Enterobacter hormaechei subsp. xiangfangensis strain ST114 plasmid pLAU_ENM30_NDM1, complete sequence	15405-15429	4	0.84
NZ_LN831776_17	17.2|1269328|25|NZ_LN831776|CRISPRCasFinder	1269328-1269352	25	NZ_CP020050	Escherichia coli strain AR_0118 plasmid unitig_2, complete sequence	71696-71720	4	0.84
NZ_LN831776_17	17.2|1269328|25|NZ_LN831776|CRISPRCasFinder	1269328-1269352	25	MN688131	Enterobacter hormaechei subsp. xiangfangensis strain ST114 plasmid pLAU_ENC1, complete sequence	8662-8686	4	0.84
NZ_LN831776_17	17.2|1269328|25|NZ_LN831776|CRISPRCasFinder	1269328-1269352	25	NZ_CP014777	Pluralibacter gergoviae strain FB2 plasmid pFB2.2, complete sequence	17317-17341	4	0.84
NZ_LN831776_17	17.2|1269328|25|NZ_LN831776|CRISPRCasFinder	1269328-1269352	25	NZ_KT852336	Klebsiella pneumoniae strain Kpn235 plasmid Kpn235-BG, complete sequence	3783-3807	4	0.84
NZ_LN831776_17	17.2|1269328|25|NZ_LN831776|CRISPRCasFinder	1269328-1269352	25	NZ_KJ958927	Klebsiella pneumoniae strain Kpn-3002cz plasmid pS-3002cz, complete sequence	26082-26106	4	0.84
NZ_LN831776_17	17.2|1269328|25|NZ_LN831776|CRISPRCasFinder	1269328-1269352	25	NZ_KT852335	Klebsiella pneumoniae subsp. pneumoniae strain 240-BG plasmid kpn240-BG, complete sequence	4090-4114	4	0.84
NZ_LN831776_17	17.2|1269328|25|NZ_LN831776|CRISPRCasFinder	1269328-1269352	25	NZ_KJ958926	Klebsiella pneumoniae strain Kpn-3002cz plasmid pB-3002cz, complete sequence	20994-21018	4	0.84
NZ_LN831776_17	17.2|1269328|25|NZ_LN831776|CRISPRCasFinder	1269328-1269352	25	NZ_CP021687	Klebsiella pneumoniae strain AR_0146 plasmid tig00001186, complete sequence	89480-89504	4	0.84
NZ_LN831776_17	17.2|1269328|25|NZ_LN831776|CRISPRCasFinder	1269328-1269352	25	NZ_CP021720	Escherichia coli strain AR_0128 plasmid tig00000793, complete sequence	10773-10797	4	0.84
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	LZ998054	JP 2017534684-A/1: Phage Therapy	39785-39810	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MK837010	Pseudomonas virus Pa204, complete genome	47465-47490	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT133562	Pseudomonas phage willy, complete genome	39770-39795	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	NC_011165	Pseudomonas phage LBL3, complete genome	39280-39305	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT108729	Pseudomonas phage Epa22, complete genome	3393-3418	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT491206	Pseudomonas phage vB_PaeM_USP_3, complete genome	40063-40088	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT491205	Pseudomonas phage vB_PaeM_USP_2, complete genome	39922-39947	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN871457	UNVERIFIED: Pseudomonas phage Pa-F, complete genome	46238-46263	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT933737	Pseudomonas phage PASA16, complete genome	11457-11482	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	NC_019451	Pseudomonas phage NH-4, complete genome	40347-40372	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT119364	Pseudomonas phage elmo, complete genome	39199-39224	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	LC102730	Pseudomonas phage S12-1 DNA, complete genome	39283-39308	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	LC472883	Pseudomonas phage S12-3 DNA, complete genome	39283-39308	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN871464	UNVERIFIED: Pseudomonas phage Pa-M, complete genome	11463-11488	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	KP340288	Pseudomonas phage phiKTN6, complete genome	39801-39826	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	FM201281	Pseudomonas phage LBL3 complete genome	39280-39305	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT119368	Pseudomonas phage shane, complete genome	39704-39729	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	KU198331	Pseudomonas phage NP3, complete genome	40578-40603	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN615701	Pseudomonas phage vB_PaeM_SMS21, complete genome	40979-41004	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	KM434184	Pseudomonas phage vB_Pae_PS44, complete genome	42121-42146	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN131142	Pseudomonas virus PA8P1, complete genome	47210-47235	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	NC_050146	Pseudomonas phage Epa7, complete genome	3109-3134	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	LQ277707	Sequence 2 from Patent WO2016071503	49115-49140	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	GU815091	Pseudomonas phage JG024, complete genome	40585-40610	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	LC472881	Pseudomonas phage R12 DNA, complete genome	16812-16837	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT119376	Pseudomonas phage chunk, complete genome	39884-39909	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT108727	Pseudomonas phage Epa11, complete genome	25393-25418	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	LQ277706	Sequence 1 from Patent WO2016071503	39785-39810	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN131141	Pseudomonas virus PaP1_EPu-2019, complete genome	47889-47914	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	AP018815	Pseudomonas phage PaGU11 DNA, complete genome	39760-39785	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT119363	Pseudomonas phage debbie, complete genome	39688-39713	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	LN610588	Pseudomonas phage vB_PaeM_PAO1_Ab29, complete genome	47957-47982	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN615700	Pseudomonas phage vB_PaeM_SMS12, complete genome	40677-40702	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	NC_019935	Pseudomonas phage KPP12 DNA, complete genome	39281-39306	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	KX171208	Pseudomonas phage vB_Pae436M-8, complete genome	40986-41011	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	LZ998055	JP 2017534684-A/2: Phage Therapy	49115-49140	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	LN610579	Pseudomonas phage vB_PaeM_PAO1_Ab27, complete genome	47826-47851	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MK318076	Pseudomonas phage vB_PaeM_fHoPae01, complete genome	47661-47686	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT119366	Pseudomonas phage jett, complete genome	39929-39954	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	NC_042079	Pseudomonas phage vB_PaeM_E217, complete genome	40353-40378	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	NC_011756	Pseudomonas phage SN, complete genome	40574-40599	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	NC_011703	Pseudomonas phage 14-1, complete genome	40501-40526	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT119365	Pseudomonas phage goodold, complete genome	39541-39566	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT491204	Pseudomonas phage vB_PaeM_USP_1, complete genome	39869-39894	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT118291	Pseudomonas phage Epa12, complete genome	10689-10714	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN131143	Pseudomonas virus PA11P1, complete genome	47471-47496	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	LC472884	Pseudomonas phage S50 DNA, complete genome	52778-52803	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT349888	Pseudomonas phage PHW2, complete genome	41729-41754	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	NC_048745	Pseudomonas phage vB_PaeM_SCUT-S1, complete genome	40365-40390	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT119369	Pseudomonas phage sortsol, complete genome	40304-40329	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN615702	Pseudomonas phage vB_PaeM_SMS29, complete genome	40804-40829	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MF623055	Pseudomonas phage BrSP1, complete genome	47123-47148	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN871466	UNVERIFIED: Pseudomonas phage Pa-O, complete genome	46261-46286	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	NC_042080	Pseudomonas phage vB_PaeM_E215, complete genome	27553-27578	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	NC_050148	Pseudomonas virus Pa193, complete genome	47813-47838	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN871485	UNVERIFIED: Pseudomonas phage PaSz-8_45_66k, complete genome	26739-26764	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN871467	UNVERIFIED: Pseudomonas phage Pa-P, complete genome	45530-45555	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	NC_041902	Pseudomonas phage PA5, complete genome	44327-44352	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN871468	UNVERIFIED: Pseudomonas phage Pa-Q, complete genome	29726-29751	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT413450	Pseudomonas phage Epa15, complete genome	54479-54504	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN871479	UNVERIFIED: Pseudomonas phage PaSt-2_45_65k, complete genome	10371-10396	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT118290	Pseudomonas phage Epa10, complete genome	13033-13058	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN871461	UNVERIFIED: Pseudomonas phage Pa-J, complete genome	62180-62205	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	NC_048676	Pseudomonas phage SL1, complete genome	31621-31646	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN871459	UNVERIFIED: Pseudomonas phage Pa-H, complete genome	54679-54704	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN871509	UNVERIFIED: Pseudomonas phage pasz5, complete genome	55126-55151	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT118298	Pseudomonas phage Epa21, complete genome	25663-25688	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	KR054033	Pseudomonas phage DL68, complete genome	34742-34767	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN871465	UNVERIFIED: Pseudomonas virus Pa-N, complete genome	54779-54804	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN871460	UNVERIFIED: Pseudomonas phage Pa-I, complete genome	28079-28104	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MT118297	Pseudomonas phage Epa20, complete genome	27995-28020	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN871487	UNVERIFIED: Pseudomonas phage PaSz-9_45_65k, complete genome	10403-10428	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	NC_048626	Pseudomonas phage PA01 DNA, nearly complete genome	54643-54668	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MN871508	UNVERIFIED: Pseudomonas phage pasz2, complete genome	55031-55056	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	NC_050147	Pseudomonas phage Epa13, complete genome	54322-54347	4	0.846
NZ_LN831776_34	34.1|2668206|26|NZ_LN831776|CRISPRCasFinder	2668206-2668231	26	MG897799	Pseudomonas phage vB_PaeM_LS1, complete genome	50933-50958	4	0.846
NZ_LN831776_40	40.5|3576201|25|NZ_LN831776|CRT	3576201-3576225	25	NZ_CP019063	Rahnella sp. ERMR1:05 plasmid unnamed1, complete sequence	459359-459383	4	0.84
NZ_LN831776_40	40.3|3576099|25|NZ_LN831776|CRT	3576099-3576123	25	NZ_CP024183	Moraxella osloensis strain KSH plasmid p3, complete sequence	26612-26636	5	0.8
NZ_LN831776_48	48.1|4912681|26|NZ_LN831776|CRISPRCasFinder	4912681-4912706	26	NZ_CP038621	Arsenophonus nasoniae strain FIN plasmid pArsFIN9, complete sequence	44282-44307	5	0.808
NZ_LN831776_48	48.1|4912681|26|NZ_LN831776|CRISPRCasFinder	4912681-4912706	26	NZ_CP038614	Arsenophonus nasoniae strain FIN plasmid pArsFIN2, complete sequence	41797-41822	5	0.808
NZ_LN831776_48	48.1|4912681|26|NZ_LN831776|CRISPRCasFinder	4912681-4912706	26	NZ_CP038614	Arsenophonus nasoniae strain FIN plasmid pArsFIN2, complete sequence	174494-174519	5	0.808
NZ_LN831776_48	48.1|4912681|26|NZ_LN831776|CRISPRCasFinder	4912681-4912706	26	NZ_CP038615	Arsenophonus nasoniae strain FIN plasmid pArsFIN3, complete sequence	14359-14384	5	0.808
NZ_LN831776_48	48.1|4912681|26|NZ_LN831776|CRISPRCasFinder	4912681-4912706	26	NZ_CP038616	Arsenophonus nasoniae strain FIN plasmid pArsFIN4, complete sequence	18828-18853	5	0.808
NZ_LN831776_48	48.1|4912681|26|NZ_LN831776|CRISPRCasFinder	4912681-4912706	26	NZ_CP038617	Arsenophonus nasoniae strain FIN plasmid pArsFIN5, complete sequence	27756-27781	5	0.808
NZ_LN831776_48	48.1|4912681|26|NZ_LN831776|CRISPRCasFinder	4912681-4912706	26	NZ_CP038620	Arsenophonus nasoniae strain FIN plasmid pArsFIN8, complete sequence	82121-82146	5	0.808
NZ_LN831776_48	48.1|4912681|26|NZ_LN831776|CRISPRCasFinder	4912681-4912706	26	NZ_CP038622	Arsenophonus nasoniae strain FIN plasmid pArsFIN10, complete sequence	44393-44418	5	0.808
NZ_LN831776_57	57.5|5507955|30|NZ_LN831776|CRT	5507955-5507984	30	MN693778	Marine virus AFVG_250M953, complete genome	5637-5666	5	0.833
NZ_LN831776_57	57.5|5507955|30|NZ_LN831776|CRT	5507955-5507984	30	MN693883	Marine virus AFVG_250M954, complete genome	5615-5644	5	0.833
NZ_LN831776_59	59.1|5654499|27|NZ_LN831776|CRISPRCasFinder	5654499-5654525	27	NZ_CP023152	Mycobacterium chimaera strain FLAC0070 plasmid pFLAC0070_1, complete sequence	185739-185765	5	0.815
NZ_LN831776_59	59.1|5654499|27|NZ_LN831776|CRISPRCasFinder	5654499-5654525	27	NZ_CP029834	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed4, complete sequence	188182-188208	5	0.815
NZ_LN831776_59	59.1|5654499|27|NZ_LN831776|CRISPRCasFinder	5654499-5654525	27	NC_010625	Paraburkholderia phymatum STM815 plasmid pBPHY01, complete sequence	1070475-1070501	5	0.815
NZ_LN831776_59	59.1|5654499|27|NZ_LN831776|CRISPRCasFinder	5654499-5654525	27	NC_013859	Azospirillum sp. B510 plasmid pAB510e, complete sequence	367916-367942	5	0.815
NZ_LN831776_59	59.1|5654499|27|NZ_LN831776|CRISPRCasFinder	5654499-5654525	27	NZ_CP054620	Azospirillum oryzae strain KACC 14407 plasmid unnamed5, complete sequence	124197-124223	5	0.815
NZ_LN831776_80	80.1|7757550|28|NZ_LN831776|CRISPRCasFinder	7757550-7757577	28	NZ_CP010421	Azotobacter chroococcum NCIMB 8003 plasmid pAcX50f, complete sequence	275658-275685	5	0.821
NZ_LN831776_5	5.2|548629|27|NZ_LN831776|CRISPRCasFinder	548629-548655	27	MG675557	Pseudoalteromonas phage Maelstrom, complete genome	34101-34127	6	0.778
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MT498035	Gordonia Phage Barsten, complete genome	1141-1173	6	0.818
NZ_LN831776_33	33.1|2627304|28|NZ_LN831776|CRISPRCasFinder	2627304-2627331	28	NC_018878	Bacillus thuringiensis Bt407 plasmid BTB_502p, complete sequence	423608-423635	6	0.786
NZ_LN831776_33	33.3|2627427|28|NZ_LN831776|CRISPRCasFinder	2627427-2627454	28	MN862339	Kummerowia striata gokushovirus strain pt119-gok-5, complete genome	84-111	6	0.786
NZ_LN831776_33	33.3|2627427|28|NZ_LN831776|CRISPRCasFinder	2627427-2627454	28	NZ_CP009619	Vibrio coralliilyticus strain RE98 plasmid p380, complete sequence	88218-88245	6	0.786
NZ_LN831776_33	33.3|2627427|28|NZ_LN831776|CRISPRCasFinder	2627427-2627454	28	NZ_CP014175	Clostridium argentinense strain 89G plasmid pRSJ17_1, complete sequence	120721-120748	6	0.786
NZ_LN831776_33	33.3|2627427|28|NZ_LN831776|CRISPRCasFinder	2627427-2627454	28	MW057857	Providencia phage PSTCR5, complete genome	66368-66395	6	0.786
NZ_LN831776_33	33.3|2627427|28|NZ_LN831776|CRISPRCasFinder	2627427-2627454	28	KY363465	Providencia phage vB_PreS_PR1, complete genome	16684-16711	6	0.786
NZ_LN831776_33	33.3|2627427|28|NZ_LN831776|CRISPRCasFinder	2627427-2627454	28	MN693059	Marine virus AFVG_25M422, complete genome	6510-6537	6	0.786
NZ_LN831776_37	37.1|2868051|28|NZ_LN831776|CRISPRCasFinder	2868051-2868078	28	NZ_CP050126	Rhodococcus erythropolis strain KB1 plasmid plas2, complete sequence	30839-30866	6	0.786
NZ_LN831776_37	37.1|2868051|28|NZ_LN831776|CRISPRCasFinder	2868051-2868078	28	NZ_CP024940	Paraburkholderia hospita strain mHSR1 plasmid pmHSR1_P, complete sequence	1090211-1090238	6	0.786
NZ_LN831776_42	42.1|3996224|28|NZ_LN831776|CRISPRCasFinder	3996224-3996251	28	NZ_CP024940	Paraburkholderia hospita strain mHSR1 plasmid pmHSR1_P, complete sequence	1090211-1090238	6	0.786
NZ_LN831776_48	48.1|4912681|26|NZ_LN831776|CRISPRCasFinder	4912681-4912706	26	KX961631	Bacillus phage QCM11, complete genome	7606-7631	6	0.769
NZ_LN831776_48	48.1|4912681|26|NZ_LN831776|CRISPRCasFinder	4912681-4912706	26	NC_049966	Bacillus phage vB_BthP-Goe4, complete genome	7774-7799	6	0.769
NZ_LN831776_59	59.1|5654499|27|NZ_LN831776|CRISPRCasFinder	5654499-5654525	27	NZ_CP032341	Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence	453170-453196	6	0.778
NZ_LN831776_59	59.1|5654499|27|NZ_LN831776|CRISPRCasFinder	5654499-5654525	27	NZ_CP032347	Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence	236995-237021	6	0.778
NZ_LN831776_59	59.1|5654499|27|NZ_LN831776|CRISPRCasFinder	5654499-5654525	27	NZ_CP012916	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence	595442-595468	6	0.778
NZ_LN831776_70	70.2|6958084|28|NZ_LN831776|CRISPRCasFinder	6958084-6958111	28	NZ_CP010764	Phaeobacter inhibens strain P80 plasmid pP80_h, complete sequence	34342-34369	6	0.786
NZ_LN831776_70	70.2|6958084|28|NZ_LN831776|CRISPRCasFinder	6958084-6958111	28	NZ_CP010764	Phaeobacter inhibens strain P80 plasmid pP80_h, complete sequence	47967-47994	6	0.786
NZ_LN831776_70	70.2|6958084|28|NZ_LN831776|CRISPRCasFinder	6958084-6958111	28	NZ_CP034351	Streptomyces sp. W1SF4 plasmid p1, complete sequence	129250-129277	6	0.786
NZ_LN831776_70	70.2|6958084|28|NZ_LN831776|CRISPRCasFinder	6958084-6958111	28	NZ_CP023408	Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence	396165-396192	6	0.786
NZ_LN831776_70	70.2|6958084|28|NZ_LN831776|CRISPRCasFinder	6958084-6958111	28	NZ_CP017105	Rhizobium gallicum strain IE4872 plasmid pRgalIE4872d, complete sequence	433038-433065	6	0.786
NZ_LN831776_70	70.2|6958084|28|NZ_LN831776|CRISPRCasFinder	6958084-6958111	28	CP006880	Rhizobium gallicum bv. gallicum R602 plasmid pRgalR602c, complete sequence	601547-601574	6	0.786
NZ_LN831776_75	75.1|7578918|27|NZ_LN831776|CRISPRCasFinder	7578918-7578944	27	NZ_CP054028	Rhizobium sp. JKLM19E plasmid pPR19E01, complete sequence	1045401-1045427	6	0.778
NZ_LN831776_1	1.1|114349|28|NZ_LN831776|CRISPRCasFinder	114349-114376	28	MN693364	Marine virus AFVG_25M258, complete genome	16101-16128	7	0.75
NZ_LN831776_8	8.1|670877|28|NZ_LN831776|CRISPRCasFinder	670877-670904	28	MN693364	Marine virus AFVG_25M258, complete genome	16101-16128	7	0.75
NZ_LN831776_20	20.1|1558504|28|NZ_LN831776|CRISPRCasFinder	1558504-1558531	28	AP013820	Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C15-MedDCM-OCT-S46-C98, *** SEQUENCING IN PROGRESS ***	27814-27841	7	0.75
NZ_LN831776_20	20.1|1558504|28|NZ_LN831776|CRISPRCasFinder	1558504-1558531	28	AP014449	Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C15-MedDCM-OCT-S28-C118, *** SEQUENCING IN PROGRESS ***, 2 ordered pieces	9790-9817	7	0.75
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MH153809	Gordonia phage Sitar, complete genome	1142-1174	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MH976518	Gordonia phage Stultus, complete genome	1141-1173	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MH976511	Gordonia phage Gaea, complete genome	1139-1171	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MK937594	Gordonia phage Galadriel, complete genome	1141-1173	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MN329673	Gordonia phage Jabberwocky, complete genome	1141-1173	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MT723934	Gordonia phage Love, complete genome	1141-1173	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MT639640	Gordonia phage Paries, complete genome	1141-1173	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MK977702	Gordonia terrae phage McKinley, complete genome	1141-1173	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	NC_042108	Gordonia phage Brandonk123, complete genome	1141-1173	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MH976508	Gordonia phage Bibwit, complete genome	1141-1173	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	NC_042045	Gordonia phage Lennon, complete genome	1142-1174	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MH976507	Gordonia phage Ailee, complete genome	1141-1173	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MH651168	Gordonia phage Ashertheman, complete genome	1139-1171	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MK967396	Gordonia phage Tangerine, complete genome	1139-1171	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	NZ_CP029455	Bacillus cereus strain FORC087 plasmid pFORC087.1, complete sequence	227418-227450	7	0.788
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MK937607	Gordonia phage Zipp, complete genome	2126-2158	7	0.788
NZ_LN831776_23	23.31|1615946|33|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR	1615946-1615978	33	NC_004768	Bifidobacterium longum RW041 plasmid pNAC3, complete sequence	7807-7839	7	0.788
NZ_LN831776_23	23.37|1616340|32|NZ_LN831776|CRT	1616340-1616371	32	NZ_CP024200	Thalassospira marina strain CSC3H3 plasmid pCSC3H3, complete sequence	191510-191541	7	0.781
NZ_LN831776_23	23.37|1616340|32|NZ_LN831776|CRT	1616340-1616371	32	NZ_CP042262	Litoreibacter sp. LN3S51 plasmid unnamed1, complete sequence	413192-413223	7	0.781
NZ_LN831776_30	30.1|2307535|27|NZ_LN831776|CRISPRCasFinder	2307535-2307561	27	NZ_CP024200	Thalassospira marina strain CSC3H3 plasmid pCSC3H3, complete sequence	866155-866181	7	0.741
NZ_LN831776_32	32.1|2606679|27|NZ_LN831776|CRISPRCasFinder	2606679-2606705	27	CP000617	Burkholderia vietnamiensis G4 plasmid pBVIE01, complete sequence	67068-67094	7	0.741
NZ_LN831776_32	32.1|2606679|27|NZ_LN831776|CRISPRCasFinder	2606679-2606705	27	NZ_CP016452	Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence	983396-983422	7	0.741
NZ_LN831776_33	33.3|2627427|28|NZ_LN831776|CRISPRCasFinder	2627427-2627454	28	NZ_AP018282	Chondrocystis sp. NIES-4102 plasmid plasmid1 DNA, complete genome	161643-161670	7	0.75
NZ_LN831776_33	33.3|2627427|28|NZ_LN831776|CRISPRCasFinder	2627427-2627454	28	NZ_CP037748	Campylobacter helveticus strain 2013D-9613 plasmid unnamed2, complete sequence	21080-21107	7	0.75
NZ_LN831776_33	33.3|2627427|28|NZ_LN831776|CRISPRCasFinder	2627427-2627454	28	NZ_CP020480	Campylobacter helveticus strain ATCC 51209 plasmid pHELV-2, complete sequence	18635-18662	7	0.75
NZ_LN831776_33	33.3|2627427|28|NZ_LN831776|CRISPRCasFinder	2627427-2627454	28	MN694638	Marine virus AFVG_250M1093, complete genome	36711-36738	7	0.75
NZ_LN831776_37	37.1|2868051|28|NZ_LN831776|CRISPRCasFinder	2868051-2868078	28	NZ_CP049038	Pseudohalocynthiibacter aestuariivivens strain RR4-35 plasmid pRR4-35_1, complete sequence	103161-103188	7	0.75
NZ_LN831776_37	37.1|2868051|28|NZ_LN831776|CRISPRCasFinder	2868051-2868078	28	NZ_CP045407	Roseovarius sp. THAF9 plasmid pTHAF9_c, complete sequence	18780-18807	7	0.75
NZ_LN831776_42	42.1|3996224|28|NZ_LN831776|CRISPRCasFinder	3996224-3996251	28	NZ_CP021367	Acidovorax carolinensis strain P4 plasmid pACP4.1, complete sequence	3156-3183	7	0.75
NZ_LN831776_42	42.1|3996224|28|NZ_LN831776|CRISPRCasFinder	3996224-3996251	28	NZ_CP021367	Acidovorax carolinensis strain P4 plasmid pACP4.1, complete sequence	262393-262420	7	0.75
NZ_LN831776_42	42.1|3996224|28|NZ_LN831776|CRISPRCasFinder	3996224-3996251	28	NZ_CP021363	Acidovorax carolinensis strain P3 plasmid pACP3.1, complete sequence	247291-247318	7	0.75
NZ_LN831776_51	51.1|5084501|33|NZ_LN831776|CRISPRCasFinder	5084501-5084533	33	NZ_CP054613	Paenibacillus cellulosilyticus strain KACC 14175 plasmid unnamed4, complete sequence	1149456-1149488	7	0.788
NZ_LN831776_57	57.1|5507775|30|NZ_LN831776|CRT	5507775-5507804	30	KX349297	Cyanophage S-RIM44 isolate W2_10_0709, complete genome	181824-181853	7	0.767
NZ_LN831776_57	57.1|5507775|30|NZ_LN831776|CRT	5507775-5507804	30	KU594607	Cyanophage S-RIM44 isolate W2_07_0710, complete genome	181542-181571	7	0.767
NZ_LN831776_57	57.1|5507775|30|NZ_LN831776|CRT	5507775-5507804	30	NC_015288	Prochlorococcus phage Syn1, complete genome	179738-179767	7	0.767
NZ_LN831776_57	57.1|5507775|30|NZ_LN831776|CRT	5507775-5507804	30	KX349295	Cyanophage S-RIM44 isolate Sn_08_0709, complete genome	181515-181544	7	0.767
NZ_LN831776_57	57.1|5507775|30|NZ_LN831776|CRT	5507775-5507804	30	KX349292	Cyanophage S-RIM44 isolate Np_05_0604, complete genome	181544-181573	7	0.767
NZ_LN831776_59	59.1|5654499|27|NZ_LN831776|CRISPRCasFinder	5654499-5654525	27	NZ_LT969519	Pseudomonas aeruginosa isolate RW109 genome assembly, plasmid: RW109 plasmid 1	454701-454727	7	0.741
NZ_LN831776_60	60.1|5681511|29|NZ_LN831776|CRISPRCasFinder	5681511-5681539	29	NZ_CP054145	Deefgea sp. D17 plasmid unnamed2, complete sequence	2614-2642	7	0.759
NZ_LN831776_62	62.1|6127671|29|NZ_LN831776|CRISPRCasFinder	6127671-6127699	29	CP047389	Agrobacterium sp. CGMCC 11546 plasmid pA	121109-121137	7	0.759
NZ_LN831776_63	63.1|6227005|29|NZ_LN831776|CRISPRCasFinder	6227005-6227033	29	NZ_CP015065	Mesorhizobium ciceri biovar biserrulae strain WSM1284 plasmid pMc1284, complete sequence	388120-388148	7	0.759
NZ_LN831776_64	64.1|6490668|28|NZ_LN831776|CRISPRCasFinder	6490668-6490695	28	CP053324	Salmonella enterica subsp. salamae serovar 40:c:e,n,z15 strain 2013K-0524 plasmid unnamed, complete sequence	25969-25996	7	0.75
NZ_LN831776_69	69.1|6944723|28|NZ_LN831776|CRISPRCasFinder	6944723-6944750	28	NZ_CP043831	Bacillus sp. BS98 plasmid unnamed1	212418-212445	7	0.75
NZ_LN831776_70	70.2|6958084|28|NZ_LN831776|CRISPRCasFinder	6958084-6958111	28	NZ_LR594668	Variovorax sp. SRS16 plasmid 3	333175-333202	7	0.75
NZ_LN831776_70	70.2|6958084|28|NZ_LN831776|CRISPRCasFinder	6958084-6958111	28	NZ_CP012748	Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence	2155529-2155556	7	0.75
NZ_LN831776_19	19.1|1507993|35|NZ_LN831776|CRISPRCasFinder	1507993-1508027	35	NZ_CP054613	Paenibacillus cellulosilyticus strain KACC 14175 plasmid unnamed4, complete sequence	1149453-1149487	8	0.771
NZ_LN831776_21	21.6|1593117|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1593117-1593151	35	MT374854	Yersinia phage vB_YpM_6, complete genome	5356-5390	8	0.771
NZ_LN831776_21	21.6|1593117|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1593117-1593151	35	MT374853	Yersinia phage vB_YpM_5, complete genome	6732-6766	8	0.771
NZ_LN831776_22	22.25|1605039|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1605039-1605073	35	NZ_CP036456	Streptomonospora sp. M2 plasmid phiM2, complete sequence	10672-10706	8	0.771
NZ_LN831776_23	23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614158-1614190	33	MH976512	Gordonia phage Geodirt, complete genome	1141-1173	8	0.758
NZ_LN831776_23	23.16|1614957|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1614957-1614990	34	NZ_AP017384	Moraxella osloensis strain KMC41 plasmid pMOSL3, complete sequence	32656-32689	8	0.765
NZ_LN831776_23	23.17|1615023|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1615023-1615056	34	NC_013155	Lactococcus phage CB13, complete genome	22037-22070	8	0.765
NZ_LN831776_23	23.17|1615023|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1615023-1615056	34	HM029250	Lactococcus phage 949, complete genome	33922-33955	8	0.765
NZ_LN831776_23	23.17|1615023|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1615023-1615056	34	KC522412	Lactococcus phage CaseusJM1, complete genome	20306-20339	8	0.765
NZ_LN831776_23	23.28|1615749|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR	1615749-1615782	34	MG065650	UNVERIFIED: Campylobacter phage B15, complete genome	86098-86131	8	0.765
NZ_LN831776_23	23.28|1615749|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR	1615749-1615782	34	LR746137	Escherichia phage vB_EcoM_UP17 genome assembly, chromosome: 1	61153-61186	8	0.765
NZ_LN831776_24	24.8|1620370|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR	1620370-1620403	34	EU717894	Xanthomonas phage phiL7, complete genome	16425-16458	8	0.765
NZ_LN831776_27	27.1|2153720|29|NZ_LN831776|CRISPRCasFinder	2153720-2153748	29	NZ_CP015065	Mesorhizobium ciceri biovar biserrulae strain WSM1284 plasmid pMc1284, complete sequence	388120-388148	8	0.724
NZ_LN831776_33	33.1|2627304|28|NZ_LN831776|CRISPRCasFinder	2627304-2627331	28	NZ_CP033935	Chryseobacterium balustinum strain KC_1863 plasmid unnamed, complete sequence	83048-83075	8	0.714
NZ_LN831776_43	43.1|4328542|29|NZ_LN831776|CRISPRCasFinder	4328542-4328570	29	NZ_CP015065	Mesorhizobium ciceri biovar biserrulae strain WSM1284 plasmid pMc1284, complete sequence	388120-388148	8	0.724
NZ_LN831776_57	57.2|5507823|30|NZ_LN831776|CRT	5507823-5507852	30	KU599879	Flavobacterium phage Fpv3, complete genome	55494-55523	8	0.733
NZ_LN831776_57	57.2|5507823|30|NZ_LN831776|CRT	5507823-5507852	30	MK764441	Flavobacterium phage FPSV-F12, complete genome	49536-49565	8	0.733
NZ_LN831776_57	57.2|5507823|30|NZ_LN831776|CRT	5507823-5507852	30	KU599886	Flavobacterium phage Fpv20, complete genome	56419-56448	8	0.733
NZ_LN831776_57	57.2|5507823|30|NZ_LN831776|CRT	5507823-5507852	30	NC_031931	Flavobacterium phage Fpv2, complete genome	56240-56269	8	0.733
NZ_LN831776_57	57.2|5507823|30|NZ_LN831776|CRT	5507823-5507852	30	KT876726	Flavobacterium phage FpV21, complete genome	56231-56260	8	0.733
NZ_LN831776_57	57.2|5507823|30|NZ_LN831776|CRT	5507823-5507852	30	KT876724	Flavobacterium phage FpV4, complete genome	55435-55464	8	0.733
NZ_LN831776_57	57.2|5507823|30|NZ_LN831776|CRT	5507823-5507852	30	KU599877	Flavobacterium phage Fpv1, complete genome	56265-56294	8	0.733
NZ_LN831776_69	69.1|6944723|28|NZ_LN831776|CRISPRCasFinder	6944723-6944750	28	MK047640	Phage NV18, complete genome	32746-32773	8	0.714
NZ_LN831776_70	70.2|6958084|28|NZ_LN831776|CRISPRCasFinder	6958084-6958111	28	NZ_CP014169	Sphingomonas panacis strain DCY99 plasmid unnamed, complete sequence	140421-140448	8	0.714
NZ_LN831776_77	77.1|7629925|29|NZ_LN831776|CRISPRCasFinder	7629925-7629953	29	NZ_CP015065	Mesorhizobium ciceri biovar biserrulae strain WSM1284 plasmid pMc1284, complete sequence	388120-388148	8	0.724
NZ_LN831776_21	21.11|1593453|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1593453-1593488	36	NZ_CP021876	Enterococcus wangshanyuanii strain MN05 plasmid unnamed3	69409-69444	9	0.75
NZ_LN831776_21	21.15|1593720|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1593720-1593753	34	NZ_CP034143	Marinobacter sp. NP-4(2019) plasmid unnamed1, complete sequence	74087-74120	9	0.735
NZ_LN831776_21	21.15|1593720|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1593720-1593753	34	JX100810	Caulobacter phage CcrColossus, complete genome	117684-117717	9	0.735
NZ_LN831776_21	21.23|1594250|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1594250-1594283	34	NZ_CP015325	Bacillus filamentosus strain Hbe603 plasmid pBEH3, complete sequence	7283-7316	9	0.735
NZ_LN831776_21	21.25|1594383|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1594383-1594416	34	NC_010625	Paraburkholderia phymatum STM815 plasmid pBPHY01, complete sequence	759552-759585	9	0.735
NZ_LN831776_22	22.2|1603508|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1603508-1603541	34	NZ_CP043613	Lactobacillus buchneri strain MGB0786 plasmid unnamed1, complete sequence	7397-7430	9	0.735
NZ_LN831776_22	22.21|1604773|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604773-1604807	35	NZ_CP016617	Microvirga ossetica strain V5/3m plasmid unnamed1, complete sequence	317384-317418	9	0.743
NZ_LN831776_22	22.25|1605039|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1605039-1605073	35	JQ680374	Unidentified phage clone 2209_scaffold441 genomic sequence	25330-25364	9	0.743
NZ_LN831776_23	23.28|1615749|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR	1615749-1615782	34	MN850571	Escherichia phage nepoznato, complete genome	148996-149029	9	0.735
NZ_LN831776_23	23.28|1615749|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR	1615749-1615782	34	MH051333	Escherichia phage vB_EcoM-Ro121c4YLVW, complete genome	56107-56140	9	0.735
NZ_LN831776_23	23.28|1615749|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR	1615749-1615782	34	NC_047776	Escherichia phage ESCO5, complete genome	68786-68819	9	0.735
NZ_LN831776_23	23.28|1615749|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR	1615749-1615782	34	NC_019521	Sphingomonas phage PAU, complete genome	75133-75166	9	0.735
NZ_LN831776_23	23.31|1615946|33|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR	1615946-1615978	33	MF153391	Escherichia phage ST2, complete genome	11209-11241	9	0.727
NZ_LN831776_23	23.35|1616209|33|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR	1616209-1616241	33	NC_009760	Bacillus phage 0305phi8-36, complete genome	201513-201545	9	0.727
NZ_LN831776_24	24.27|1621634|32|NZ_LN831776|CRT	1621634-1621665	32	NZ_CP034431	Bradyrhizobium sp. LCT2 plasmid pLCT2, complete sequence	45722-45753	9	0.719
NZ_LN831776_21	21.1|1592787|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1592787-1592820	34	KU878088	Bacillus phage AR9, complete genome	55575-55608	10	0.706
NZ_LN831776_21	21.1|1592787|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1592787-1592820	34	MF360957	Bacillus virus PBS1, complete genome	216225-216258	10	0.706
NZ_LN831776_22	22.8|1603905|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1603905-1603937	33	NZ_LT984809	Cupriavidus taiwanensis isolate Cupriavidus taiwanensis STM 8555 plasmid I, complete sequence	367701-367733	10	0.697
NZ_LN831776_23	23.17|1615023|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1615023-1615056	34	NZ_CP039845	Acetobacter pasteurianus strain CICC 22518 plasmid pAP22518-1, complete sequence	453742-453775	10	0.706
NZ_LN831776_24	24.6|1620236|34|NZ_LN831776|CRISPRCasFinder,CRT	1620236-1620269	34	NZ_CP028970	Aminobacter sp. MSH1 plasmid pUSP2, complete sequence	151310-151343	10	0.706
NZ_LN831776_21	21.3|1592919|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1592919-1592952	34	NZ_CP013615	Clostridium perfringens strain JP838 plasmid pJFP838A, complete sequence	36257-36290	11	0.676
NZ_LN831776_21	21.25|1594383|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1594383-1594416	34	NZ_CP038238	Leisingera sp. NJS201 plasmid unnamed4, complete sequence	113541-113574	11	0.676
NZ_LN831776_21	21.25|1594383|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1594383-1594416	34	NZ_CP035421	Leisingera sp. NJS204 plasmid unnamed4, complete sequence	338-371	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_KX710093	Leclercia adecarboxylata strain pP10164 plasmid pP10164-2, complete sequence	280666-280699	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_KY270852	Enterobacter cloacae strain T5282 plasmid pT5282-mphA, complete sequence	256323-256356	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_KY270851	Citrobacter freundii strain 112298 plasmid p112298-catA, complete sequence	229702-229735	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_LN830952	Enterobacter sp. 247 strain 247 BMC plasmid pEB247, complete sequence	265334-265367	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP028537	Enterobacter hormaechei strain SCEH020042 plasmid pQnrB4_020042, complete sequence	295165-295198	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP048350	Raoultella ornithinolytica strain 23 plasmid p23_A-OXA140, complete sequence	246128-246161	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP044256	Salmonella enterica strain CFSAN096147 plasmid pCFSAN096147, complete sequence	276956-276989	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP035634	Enterobacter cloacae strain EN3600 plasmid unnamed2, complete sequence	253077-253110	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP042506	Leclercia adecarboxylata strain E1 plasmid pE1_001, complete sequence	320104-320137	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	MT077884	Escherichia coli plasmid p33, complete sequence	267190-267223	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	MT077886	Escherichia coli plasmid p39, complete sequence	255542-255575	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	MN423361	Leclercia sp. strain 1106151 plasmid p1106151-mcr, complete sequence	245857-245890	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP025277	Salmonella enterica subsp. enterica strain USDA-ARS-USMARC-60984 plasmid pSJO-60984, complete sequence	233192-233225	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	MH909331	Leclercia adecarboxylata plasmid p707804-NDM, complete sequence	275528-275561	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP008825	UNVERIFIED_ORG: Enterobacter cloacae ECNIH2 plasmid pKPC-272, complete sequence	244179-244212	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP022696	Citrobacter farmeri strain AUSMDU00008141 plasmid pAUSMDU8141-1, complete sequence	295332-295365	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP052871	Enterobacter cloacae strain 3849 plasmid p3846_IncHI2_mcr, complete sequence	86254-86287	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	CP049311	Salmonella enterica subsp. enterica serovar Heidelberg strain CVM N53023 plasmid pN53023, complete sequence	180800-180833	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_LT991958	Enterobacter cloacae complex sp. isolate C45 plasmid pC45-VIM4	265454-265487	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP043855	Enterobacter hormaechei strain EB_P6_L3_02.19 plasmid unnamed2, complete sequence	91500-91533	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP044215	Klebsiella aerogenes strain KA_P10_L5_03.19 plasmid pIMPIncH12_334kb, complete sequence	331762-331795	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	CP049309	Salmonella enterica subsp. enterica serovar Johannesburg strain CVM N58011 plasmid p58011, complete sequence	75459-75492	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NC_010870	Klebsiella pneumoniae plasmid pK29, complete sequence	233686-233719	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP024813	Enterobacter sp. CRENT-193 plasmid pCRENT-193_1, complete sequence	286918-286951	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	CP049307	Salmonella enterica subsp. enterica serovar Heidelberg strain CVM N58631 plasmid p58631, complete sequence	31806-31839	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP042494	Leclercia adecarboxylata strain E61 plasmid pE61_001, complete sequence	320104-320137	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP040696	Citrobacter freundii strain R47 plasmid pR47-309, complete sequence	226672-226705	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP042552	Enterobacter hormaechei strain C45 plasmid pC45_001, complete sequence	254996-255029	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP039271	Salmonella enterica subsp. enterica serovar Senftenberg str. CFSAN004025 plasmid pCFSAN004025.1, complete sequence	290511-290544	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP016526	Salmonella enterica subsp. enterica serovar Heidelberg strain 09-036813-1A plasmid p09-036813-1A_261, complete sequence	61692-61725	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	CP050163	Escherichia coli plasmid Carbapenemase(KPC-2)_IncHI2, complete sequence	255605-255638	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP041734	Enterobacter hormaechei subsp. steigerwaltii strain ME-1 plasmid pME-1a, complete sequence	242857-242890	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	MK933279	Enterobacter hormaechei strain SCNJ07 plasmid pMCR-SCNJ07, complete sequence	63844-63877	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	LC532224	Enterobacter hormaechei subsp. xiangfangensis A2483 plasmid pA2483mcr-9 DNA, complete sequence	255032-255065	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	LC532226	Enterobacter hormaechei subsp. xiangfangensis A2504 plasmid pA2504mcr-9 DNA, complete sequence	243263-243296	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NC_005211	Serratia marcescens plasmid R478, complete sequence	241473-241506	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP026661	Salmonella enterica subsp. enterica strain 15-SA01028 plasmid pSE15-SA01028, complete sequence	243924-243957	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	LN794248	Salmonella enterica subsp. enterica serovar Typhimurium plasmid incHI2, complete sequence	83062-83095	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP029248	Enterobacter hormaechei subsp. xiangfangensis strain OSUVMCKPC4-2 plasmid pOSUEC_D, complete sequence	320593-320626	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP043927	Klebsiella quasipneumoniae subsp. quasipneumoniae strain M17277 plasmid p17277A_477, complete sequence	443677-443710	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP031102	Leclercia sp. W17 plasmid pW17-1, complete sequence	52722-52755	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP012170	Enterobacter hormaechei subsp. steigerwaltii strain 34977 plasmid p34977-263.138kb, complete sequence	171167-171200	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	LC542971	Escherichia coli IOMTU413 plasmid pIOMTU413 DNA, complete sequence	241474-241507	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	LC542972	Escherichia coli IOMTU792 plasmid pIOMTU792 DNA, complete sequence	259838-259871	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	CP051274	Salmonella enterica subsp. enterica serovar Worthington strain OLF-FSR1_WB_Partridge_SW-37 plasmid pSW37-267109, complete sequence	100343-100376	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NC_024983	Salmonella enterica subsp. enterica serovar Typhimurium plasmid pSTm-A54650, strain A54560, complete sequence	275742-275775	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	CP051271	Salmonella enterica subsp. enterica serovar Worthington strain OLF-FSR1_WB_Quail_SW-70 plasmid pSW37-267106, complete sequence	83730-83763	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP013215	Klebsiella pneumoniae subsp. pneumoniae strain H11 plasmid pH11, complete sequence	3838-3871	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP021463	Salmonella enterica subsp. enterica serovar Typhimurium strain UGA14 plasmid pUGA14_1, complete sequence	121762-121795	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NC_012556	Enterobacter cloacae plasmid pEC-IMPQ, complete sequence	290840-290873	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NC_012555	Enterobacter cloacae plasmid pEC-IMP, complete sequence	285119-285152	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP042579	Enterobacter kobei strain C16 plasmid pC16_001, complete sequence	240912-240945	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP049193	Enterobacter hormaechei strain Y2152 plasmid pIHI2-2152, complete sequence	254800-254833	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP051135	Enterobacter hormaechei strain AMS-38 plasmid pAMS-38c, complete sequence	36716-36749	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP032842	Enterobacter hormaechei strain C15117 plasmid pSPRC-Echo1, complete sequence	306257-306290	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP042525	Citrobacter freundii strain E11 plasmid pE11_001, complete sequence	302007-302040	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_LT991955	Enterobacter hormaechei subsp. steigerwaltii isolate C309 plasmid pC309-VIM4	220614-220647	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP022533	Enterobacter hormaechei strain MS7884A plasmid pMS7884A, complete sequence	198048-198081	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP038659	Citrobacter freundii strain 680 plasmid p680_1, complete sequence	200082-200115	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP029717	UNVERIFIED_ORG: Enterobacter cloacae strain AR_0154 plasmid unnamed4, complete sequence	58115-58148	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP024910	Enterobacter hormaechei subsp. xiangfangensis strain OSUKPC4_L plasmid pOSUKPC4, complete sequence	318143-318176	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	MN937241	Enterobacter cloacae strain BSI034 plasmid pBSI034-MCR9, complete sequence	244854-244887	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP042489	Enterobacter hormaechei strain C15 plasmid pC15_001, complete sequence	306518-306551	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_MN540571	Escherichia coli strain E.coli4feg plasmid pIV_IncHI2_CTX_M_15, complete sequence	43798-43831	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP033103	Enterobacter hormaechei strain L51 plasmid pEHZJ1, complete sequence	310255-310288	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_MH829594	Enterobacter cloacae strain EC62 plasmid pIMP-4-EC62, complete sequence	280404-280437	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_MK736669	Enterobacter cloacae strain EclC2185 plasmid pEclC2185CTXM15, complete sequence	93398-93431	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_LC511997	Enterobacter hormaechei subsp. xiangfangensis strain MY460 plasmid pMY460-rmtE, complete sequence	312618-312651	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_MF344580	Enterobacter cloacae strain 30860 plasmid p30860-HI2, complete sequence	215578-215611	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_MF344581	Enterobacter cloacae strain 13E573 plasmid p13E573-HI2, complete sequence	254964-254997	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_MF344583	Enterobacter cloacae strain N1863 plasmid pN1863-HI2, complete sequence	324097-324130	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_KY863418	Enterobacter asburiae strain AMA 497 plasmid pOXA436, complete sequence	280474-280507	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_KY978628	Cronobacter sakazakii strain 505108 plasmid p505108-MDR, complete sequence	279217-279250	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_MF788071	Raoultella ornithinolytica strain 23141 plasmid p23141-3, complete sequence	218312-218345	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP031724	Enterobacter hormaechei strain WCHEH020038 plasmid pCTXM9_020038, complete sequence	262917-262950	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP053191	Enterobacter hormaechei strain EGYMCRVIM plasmid pMS-37a, complete sequence	237252-237285	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_KX810825	Salmonella enterica subsp. enterica serovar Typhimurium strain MU1 plasmid pIMP4-SEM1, complete sequence	20213-20246	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_KP975077	Enterobacter cloacae strain MRSN17626 plasmid pMRVIM0813, complete sequence	243232-243265	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP028197	Salmonella enterica subsp. enterica serovar Concord strain CFSAN018747 plasmid pGMI14-002_1, complete sequence	158063-158096	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP011601	Phytobacter ursingii strain CAV1151 plasmid pCAV1151-296, complete sequence	157132-157165	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP028975	Cronobacter sakazakii strain GZcsf-1 plasmid pGW1, complete sequence	323162-323195	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP019559	Escherichia coli strain KSC207 plasmid pMRGN207, complete sequence	92573-92606	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP048293	Escherichia coli strain CVM N18EC0432 plasmid pN18EC0432-1, complete sequence	33754-33787	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP020529	Enterobacter cloacae strain 174 plasmid unnamed1, complete sequence	219692-219725	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP031567	Enterobacter hormaechei strain 2013_1a plasmid pIncHI2-1301491, complete sequence	153477-153510	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP040888	Leclercia adecarboxylata strain Z96-1 plasmid pZ96-1_1, complete sequence	113093-113126	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP042616	Escherichia coli strain NCYU-26-73 plasmid pNCYU-26-73-1, complete sequence	237612-237645	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP029037	Salmonella enterica subsp. enterica serovar Senftenberg str. 361154004 plasmid unnamed, complete sequence	285945-285978	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP030186	Salmonella enterica strain SA20094620 plasmid pSA20094620.1, complete sequence	16623-16656	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP023570	Enterobacter hormaechei strain BW plasmid unnamed2, complete sequence	20223-20256	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NC_021845	Salmonella enterica subsp. enterica serovar Cubana str. CFSAN002050 plasmid unnamed, complete sequence	102029-102062	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP027144	Enterobacter hormaechei subsp. hoffmannii strain AR_0365 plasmid unnamed1, complete sequence	1697-1730	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP049189	Enterobacter hormaechei strain Y323 plasmid pIHI2-323, complete sequence	279301-279334	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_AP018352	Enterobacter hormaechei strain TUM11043 plasmid pMTY11043_IncHI2, complete sequence	20223-20256	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP038654	Citrobacter freundii strain 154 plasmid p154_1, complete sequence	129500-129533	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP038657	Citrobacter freundii strain 565 plasmid p565_1, complete sequence	134062-134095	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP044051	Klebsiella variicola strain FDAARGOS_627 plasmid unnamed2, complete sequence	44936-44969	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_MH105051	Salmonella enterica subsp. enterica serovar Lomita strain SL131 plasmid pSL131_IncHI2, complete sequence	72920-72953	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_CP049047	Enterobacter hormaechei strain Y233 plasmid pIHI2-233, complete sequence	228793-228826	11	0.676
NZ_LN831776_22	22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT	1604973-1605006	34	NZ_MG878867	Escherichia coli strain Ec21617 plasmid pEc21617-310, complete sequence	34780-34813	11	0.676
NZ_LN831776_24	24.27|1621634|32|NZ_LN831776|CRT	1621634-1621665	32	NZ_CP015237	Rhodococcus fascians D188 plasmid unnamed2, complete sequence	36621-36652	11	0.656

1. spacer 17.1|1269276|25|NZ_LN831776|CRISPRCasFinder matches to NC_009507 (Sphingomonas wittichii RW1 plasmid pSWIT01, complete sequence) position: , mismatch: 3, identity: 0.88

ggccggaaatccgcagccagtgggt	CRISPR spacer
acccggaaatcggcagccagtgggt	Protospacer
. ********* *************

2. spacer 14.1|1028406|25|NZ_LN831776|CRISPRCasFinder matches to NZ_CP029833 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed3, complete sequence) position: , mismatch: 4, identity: 0.84

gagcgctgaaggccggttcgcccgg	CRISPR spacer
tggcgctgacggccggttcggccgg	Protospacer
 .******* ********** ****

3. spacer 14.1|1028406|25|NZ_LN831776|CRISPRCasFinder matches to KY940711 (Bradyrhizobium phage BDU-MI-1, complete genome) position: , mismatch: 4, identity: 0.84

gagcgctgaaggccggttcgcccgg	CRISPR spacer
aagcgctcaaggccggttcggccgt	Protospacer
.****** ************ *** 

4. spacer 17.2|1269328|25|NZ_LN831776|CRISPRCasFinder matches to MN792917 (Enterobacter hormaechei subsp. xiangfangensis strain ST114 plasmid pLAU_ENM30_NDM1, complete sequence) position: , mismatch: 4, identity: 0.84

ggctggaaatccgctgtgagcgtgc	CRISPR spacer
ggctggagatccgctgtgagcgaag	Protospacer
*******.************** . 

5. spacer 17.2|1269328|25|NZ_LN831776|CRISPRCasFinder matches to NZ_CP020050 (Escherichia coli strain AR_0118 plasmid unitig_2, complete sequence) position: , mismatch: 4, identity: 0.84

ggctggaaatccgctgtgagcgtgc	CRISPR spacer
ggctggagatccgctgtgagcgaag	Protospacer
*******.************** . 

6. spacer 17.2|1269328|25|NZ_LN831776|CRISPRCasFinder matches to MN688131 (Enterobacter hormaechei subsp. xiangfangensis strain ST114 plasmid pLAU_ENC1, complete sequence) position: , mismatch: 4, identity: 0.84

ggctggaaatccgctgtgagcgtgc	CRISPR spacer
ggctggagatccgctgtgagcgaag	Protospacer
*******.************** . 

7. spacer 17.2|1269328|25|NZ_LN831776|CRISPRCasFinder matches to NZ_CP014777 (Pluralibacter gergoviae strain FB2 plasmid pFB2.2, complete sequence) position: , mismatch: 4, identity: 0.84

ggctggaaatccgctgtgagcgtgc	CRISPR spacer
ggctggagatccgctgtgagcgaag	Protospacer
*******.************** . 

8. spacer 17.2|1269328|25|NZ_LN831776|CRISPRCasFinder matches to NZ_KT852336 (Klebsiella pneumoniae strain Kpn235 plasmid Kpn235-BG, complete sequence) position: , mismatch: 4, identity: 0.84

ggctggaaatccgctgtgagcgtgc	CRISPR spacer
ggctggagatccgctgtgagcgaag	Protospacer
*******.************** . 

9. spacer 17.2|1269328|25|NZ_LN831776|CRISPRCasFinder matches to NZ_KJ958927 (Klebsiella pneumoniae strain Kpn-3002cz plasmid pS-3002cz, complete sequence) position: , mismatch: 4, identity: 0.84

ggctggaaatccgctgtgagcgtgc	CRISPR spacer
ggctggagatccgctgtgagcgaag	Protospacer
*******.************** . 

10. spacer 17.2|1269328|25|NZ_LN831776|CRISPRCasFinder matches to NZ_KT852335 (Klebsiella pneumoniae subsp. pneumoniae strain 240-BG plasmid kpn240-BG, complete sequence) position: , mismatch: 4, identity: 0.84

ggctggaaatccgctgtgagcgtgc	CRISPR spacer
ggctggagatccgctgtgagcgaag	Protospacer
*******.************** . 

11. spacer 17.2|1269328|25|NZ_LN831776|CRISPRCasFinder matches to NZ_KJ958926 (Klebsiella pneumoniae strain Kpn-3002cz plasmid pB-3002cz, complete sequence) position: , mismatch: 4, identity: 0.84

ggctggaaatccgctgtgagcgtgc	CRISPR spacer
ggctggagatccgctgtgagcgaag	Protospacer
*******.************** . 

12. spacer 17.2|1269328|25|NZ_LN831776|CRISPRCasFinder matches to NZ_CP021687 (Klebsiella pneumoniae strain AR_0146 plasmid tig00001186, complete sequence) position: , mismatch: 4, identity: 0.84

ggctggaaatccgctgtgagcgtgc	CRISPR spacer
ggctggagatccgctgtgagcgaag	Protospacer
*******.************** . 

13. spacer 17.2|1269328|25|NZ_LN831776|CRISPRCasFinder matches to NZ_CP021720 (Escherichia coli strain AR_0128 plasmid tig00000793, complete sequence) position: , mismatch: 4, identity: 0.84

ggctggaaatccgctgtgagcgtgc	CRISPR spacer
ggctggagatccgctgtgagcgaag	Protospacer
*******.************** . 

14. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to LZ998054 (JP 2017534684-A/1: Phage Therapy) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

15. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MK837010 (Pseudomonas virus Pa204, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

16. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT133562 (Pseudomonas phage willy, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

17. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to NC_011165 (Pseudomonas phage LBL3, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

18. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT108729 (Pseudomonas phage Epa22, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

19. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT491206 (Pseudomonas phage vB_PaeM_USP_3, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

20. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT491205 (Pseudomonas phage vB_PaeM_USP_2, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

21. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN871457 (UNVERIFIED: Pseudomonas phage Pa-F, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

22. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT933737 (Pseudomonas phage PASA16, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

23. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to NC_019451 (Pseudomonas phage NH-4, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

24. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT119364 (Pseudomonas phage elmo, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

25. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to LC102730 (Pseudomonas phage S12-1 DNA, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

26. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to LC472883 (Pseudomonas phage S12-3 DNA, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

27. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN871464 (UNVERIFIED: Pseudomonas phage Pa-M, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

28. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to KP340288 (Pseudomonas phage phiKTN6, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

29. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to FM201281 (Pseudomonas phage LBL3 complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

30. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT119368 (Pseudomonas phage shane, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

31. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to KU198331 (Pseudomonas phage NP3, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

32. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN615701 (Pseudomonas phage vB_PaeM_SMS21, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

33. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to KM434184 (Pseudomonas phage vB_Pae_PS44, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

34. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN131142 (Pseudomonas virus PA8P1, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

35. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to NC_050146 (Pseudomonas phage Epa7, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

36. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to LQ277707 (Sequence 2 from Patent WO2016071503) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

37. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to GU815091 (Pseudomonas phage JG024, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

38. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to LC472881 (Pseudomonas phage R12 DNA, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

39. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT119376 (Pseudomonas phage chunk, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

40. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT108727 (Pseudomonas phage Epa11, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

41. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to LQ277706 (Sequence 1 from Patent WO2016071503) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

42. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN131141 (Pseudomonas virus PaP1_EPu-2019, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

43. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to AP018815 (Pseudomonas phage PaGU11 DNA, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

44. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT119363 (Pseudomonas phage debbie, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

45. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to LN610588 (Pseudomonas phage vB_PaeM_PAO1_Ab29, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

46. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN615700 (Pseudomonas phage vB_PaeM_SMS12, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

47. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to NC_019935 (Pseudomonas phage KPP12 DNA, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

48. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to KX171208 (Pseudomonas phage vB_Pae436M-8, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

49. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to LZ998055 (JP 2017534684-A/2: Phage Therapy) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

50. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to LN610579 (Pseudomonas phage vB_PaeM_PAO1_Ab27, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

51. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MK318076 (Pseudomonas phage vB_PaeM_fHoPae01, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

52. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT119366 (Pseudomonas phage jett, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

53. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to NC_042079 (Pseudomonas phage vB_PaeM_E217, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

54. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to NC_011756 (Pseudomonas phage SN, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

55. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to NC_011703 (Pseudomonas phage 14-1, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

56. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT119365 (Pseudomonas phage goodold, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

57. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT491204 (Pseudomonas phage vB_PaeM_USP_1, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

58. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT118291 (Pseudomonas phage Epa12, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

59. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN131143 (Pseudomonas virus PA11P1, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

60. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to LC472884 (Pseudomonas phage S50 DNA, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

61. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT349888 (Pseudomonas phage PHW2, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

62. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to NC_048745 (Pseudomonas phage vB_PaeM_SCUT-S1, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

63. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT119369 (Pseudomonas phage sortsol, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

64. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN615702 (Pseudomonas phage vB_PaeM_SMS29, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

65. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MF623055 (Pseudomonas phage BrSP1, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

66. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN871466 (UNVERIFIED: Pseudomonas phage Pa-O, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

67. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to NC_042080 (Pseudomonas phage vB_PaeM_E215, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

68. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to NC_050148 (Pseudomonas virus Pa193, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

69. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN871485 (UNVERIFIED: Pseudomonas phage PaSz-8_45_66k, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

70. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN871467 (UNVERIFIED: Pseudomonas phage Pa-P, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

71. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to NC_041902 (Pseudomonas phage PA5, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

72. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN871468 (UNVERIFIED: Pseudomonas phage Pa-Q, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

73. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT413450 (Pseudomonas phage Epa15, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

74. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN871479 (UNVERIFIED: Pseudomonas phage PaSt-2_45_65k, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

75. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT118290 (Pseudomonas phage Epa10, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

76. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN871461 (UNVERIFIED: Pseudomonas phage Pa-J, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

77. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to NC_048676 (Pseudomonas phage SL1, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

78. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN871459 (UNVERIFIED: Pseudomonas phage Pa-H, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

79. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN871509 (UNVERIFIED: Pseudomonas phage pasz5, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

80. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT118298 (Pseudomonas phage Epa21, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

81. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to KR054033 (Pseudomonas phage DL68, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

82. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN871465 (UNVERIFIED: Pseudomonas virus Pa-N, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

83. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN871460 (UNVERIFIED: Pseudomonas phage Pa-I, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

84. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MT118297 (Pseudomonas phage Epa20, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

85. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN871487 (UNVERIFIED: Pseudomonas phage PaSz-9_45_65k, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

86. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to NC_048626 (Pseudomonas phage PA01 DNA, nearly complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

87. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MN871508 (UNVERIFIED: Pseudomonas phage pasz2, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

88. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to NC_050147 (Pseudomonas phage Epa13, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

89. spacer 34.1|2668206|26|NZ_LN831776|CRISPRCasFinder matches to MG897799 (Pseudomonas phage vB_PaeM_LS1, complete genome) position: , mismatch: 4, identity: 0.846

agcggccgggttgcccagaaacaaca	CRISPR spacer
tgcggccgggttgcccaggaacacct	Protospacer
 *****************.**** * 

90. spacer 40.5|3576201|25|NZ_LN831776|CRT matches to NZ_CP019063 (Rahnella sp. ERMR1:05 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.84

ctggcgcaagcgggctgatgagcgg	CRISPR spacer
gcggcgcaaccgggctgatgaccgg	Protospacer
 .******* *********** ***

91. spacer 40.3|3576099|25|NZ_LN831776|CRT matches to NZ_CP024183 (Moraxella osloensis strain KSH plasmid p3, complete sequence) position: , mismatch: 5, identity: 0.8

ttgaagcaaacgggtaaaagggggg	CRISPR spacer
atgaatcaaacgggtaaaagggaaa	Protospacer
 **** ****************...

92. spacer 48.1|4912681|26|NZ_LN831776|CRISPRCasFinder matches to NZ_CP038621 (Arsenophonus nasoniae strain FIN plasmid pArsFIN9, complete sequence) position: , mismatch: 5, identity: 0.808

ataaaagattaagatcaaaacacctc	CRISPR spacer
tagaaatattaagttcaaaacacctc	Protospacer
  .*** ****** ************

93. spacer 48.1|4912681|26|NZ_LN831776|CRISPRCasFinder matches to NZ_CP038614 (Arsenophonus nasoniae strain FIN plasmid pArsFIN2, complete sequence) position: , mismatch: 5, identity: 0.808

ataaaagattaagatcaaaacacctc	CRISPR spacer
tagaaatattaagttcaaaacacctc	Protospacer
  .*** ****** ************

94. spacer 48.1|4912681|26|NZ_LN831776|CRISPRCasFinder matches to NZ_CP038614 (Arsenophonus nasoniae strain FIN plasmid pArsFIN2, complete sequence) position: , mismatch: 5, identity: 0.808

ataaaagattaagatcaaaacacctc	CRISPR spacer
tagaaatattaagttcaaaacacctc	Protospacer
  .*** ****** ************

95. spacer 48.1|4912681|26|NZ_LN831776|CRISPRCasFinder matches to NZ_CP038615 (Arsenophonus nasoniae strain FIN plasmid pArsFIN3, complete sequence) position: , mismatch: 5, identity: 0.808

ataaaagattaagatcaaaacacctc	CRISPR spacer
tagaaatattaagttcaaaacacctc	Protospacer
  .*** ****** ************

96. spacer 48.1|4912681|26|NZ_LN831776|CRISPRCasFinder matches to NZ_CP038616 (Arsenophonus nasoniae strain FIN plasmid pArsFIN4, complete sequence) position: , mismatch: 5, identity: 0.808

ataaaagattaagatcaaaacacctc	CRISPR spacer
tagaaatattaagttcaaaacacctc	Protospacer
  .*** ****** ************

97. spacer 48.1|4912681|26|NZ_LN831776|CRISPRCasFinder matches to NZ_CP038617 (Arsenophonus nasoniae strain FIN plasmid pArsFIN5, complete sequence) position: , mismatch: 5, identity: 0.808

ataaaagattaagatcaaaacacctc	CRISPR spacer
tagaaatattaagttcaaaacacctc	Protospacer
  .*** ****** ************

98. spacer 48.1|4912681|26|NZ_LN831776|CRISPRCasFinder matches to NZ_CP038620 (Arsenophonus nasoniae strain FIN plasmid pArsFIN8, complete sequence) position: , mismatch: 5, identity: 0.808

ataaaagattaagatcaaaacacctc	CRISPR spacer
tagaaatattaagttcaaaacacctc	Protospacer
  .*** ****** ************

99. spacer 48.1|4912681|26|NZ_LN831776|CRISPRCasFinder matches to NZ_CP038622 (Arsenophonus nasoniae strain FIN plasmid pArsFIN10, complete sequence) position: , mismatch: 5, identity: 0.808

ataaaagattaagatcaaaacacctc	CRISPR spacer
tagaaatattaagttcaaaacacctc	Protospacer
  .*** ****** ************

100. spacer 57.5|5507955|30|NZ_LN831776|CRT matches to MN693778 (Marine virus AFVG_250M953, complete genome) position: , mismatch: 5, identity: 0.833

tggagacataggtgcagacataggtgcagt	CRISPR spacer
ggcaggcataggtgcaggcataggtgcagg	Protospacer
 * **.***********.*********** 

101. spacer 57.5|5507955|30|NZ_LN831776|CRT matches to MN693883 (Marine virus AFVG_250M954, complete genome) position: , mismatch: 5, identity: 0.833

tggagacataggtgcagacataggtgcagt	CRISPR spacer
ggcaggcataggtgcaggcataggtgcagg	Protospacer
 * **.***********.*********** 

102. spacer 59.1|5654499|27|NZ_LN831776|CRISPRCasFinder matches to NZ_CP023152 (Mycobacterium chimaera strain FLAC0070 plasmid pFLAC0070_1, complete sequence) position: , mismatch: 5, identity: 0.815

ttttcgggcaagctggccttcgacgac	CRISPR spacer
gtcaccggcaagctggtcttcgacgac	Protospacer
 *. * **********.**********

103. spacer 59.1|5654499|27|NZ_LN831776|CRISPRCasFinder matches to NZ_CP029834 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed4, complete sequence) position: , mismatch: 5, identity: 0.815

ttttcgggcaagctggccttcgacgac	CRISPR spacer
gatgccggcaagctggccttcgccgac	Protospacer
  * * **************** ****

104. spacer 59.1|5654499|27|NZ_LN831776|CRISPRCasFinder matches to NC_010625 (Paraburkholderia phymatum STM815 plasmid pBPHY01, complete sequence) position: , mismatch: 5, identity: 0.815

ttttcgggcaagctggccttcgacgac	CRISPR spacer
catgccggcaagctggccgtcgacgac	Protospacer
. * * ************ ********

105. spacer 59.1|5654499|27|NZ_LN831776|CRISPRCasFinder matches to NC_013859 (Azospirillum sp. B510 plasmid pAB510e, complete sequence) position: , mismatch: 5, identity: 0.815

ttttcgggcaagctggccttcgacgac	CRISPR spacer
gatgccggcaagctggccttcgccgac	Protospacer
  * * **************** ****

106. spacer 59.1|5654499|27|NZ_LN831776|CRISPRCasFinder matches to NZ_CP054620 (Azospirillum oryzae strain KACC 14407 plasmid unnamed5, complete sequence) position: , mismatch: 5, identity: 0.815

ttttcgggcaagctggccttcgacgac	CRISPR spacer
gatgccggcaagctggccttcgccgac	Protospacer
  * * **************** ****

107. spacer 80.1|7757550|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP010421 (Azotobacter chroococcum NCIMB 8003 plasmid pAcX50f, complete sequence) position: , mismatch: 5, identity: 0.821

tgctcgaacgccctgttctccgcaggtt	CRISPR spacer
ccctcgaaagccctgttcgccgcaggta	Protospacer
. ****** ********* ******** 

108. spacer 5.2|548629|27|NZ_LN831776|CRISPRCasFinder matches to MG675557 (Pseudoalteromonas phage Maelstrom, complete genome) position: , mismatch: 6, identity: 0.778

agcctgtccagcctgttcaacactcac	CRISPR spacer
agcctgtccagccttttcaactagctt	Protospacer
************** ******   * .

109. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MT498035 (Gordonia Phage Barsten, complete genome) position: , mismatch: 6, identity: 0.818

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgatctcgcc	Protospacer
.**********************.***.* ..*

110. spacer 33.1|2627304|28|NZ_LN831776|CRISPRCasFinder matches to NC_018878 (Bacillus thuringiensis Bt407 plasmid BTB_502p, complete sequence) position: , mismatch: 6, identity: 0.786

ccagcaaaatatgcagaaaaccgtgagt	CRISPR spacer
atactaaaatatgcagaaaaccctgaat	Protospacer
 .* .***************** ***.*

111. spacer 33.3|2627427|28|NZ_LN831776|CRISPRCasFinder matches to MN862339 (Kummerowia striata gokushovirus strain pt119-gok-5, complete genome) position: , mismatch: 6, identity: 0.786

ttctaaaaaagaacaaaatagtgaaaat	CRISPR spacer
ttctaaaaaaaaacaaaatcgtgattta	Protospacer
**********.******** ****    

112. spacer 33.3|2627427|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP009619 (Vibrio coralliilyticus strain RE98 plasmid p380, complete sequence) position: , mismatch: 6, identity: 0.786

ttctaaaaaagaacaaaatagtgaaaat	CRISPR spacer
gtcgaaaaaagaacaaaatactgacaca	Protospacer
 ** **************** *** *  

113. spacer 33.3|2627427|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP014175 (Clostridium argentinense strain 89G plasmid pRSJ17_1, complete sequence) position: , mismatch: 6, identity: 0.786

ttctaaaaaagaacaaaatagtgaaaat	CRISPR spacer
tggagaaaaagaaaaaaatagtaaaaat	Protospacer
*   .******** ********.*****

114. spacer 33.3|2627427|28|NZ_LN831776|CRISPRCasFinder matches to MW057857 (Providencia phage PSTCR5, complete genome) position: , mismatch: 6, identity: 0.786

ttctaaaaaagaacaaaatagtgaaaat	CRISPR spacer
acttaaaaaagaactagatagtgaaatt	Protospacer
 ..*********** *.********* *

115. spacer 33.3|2627427|28|NZ_LN831776|CRISPRCasFinder matches to KY363465 (Providencia phage vB_PreS_PR1, complete genome) position: , mismatch: 6, identity: 0.786

ttctaaaaaagaacaaaatagtgaaaat	CRISPR spacer
acttaaaaaagaactagatagtgaaatt	Protospacer
 ..*********** *.********* *

116. spacer 33.3|2627427|28|NZ_LN831776|CRISPRCasFinder matches to MN693059 (Marine virus AFVG_25M422, complete genome) position: , mismatch: 6, identity: 0.786

ttctaaaaaagaacaaaatagtgaaaat	CRISPR spacer
agcgaaaaaagaacaaactagtgaacaa	Protospacer
  * ************* ******* * 

117. spacer 37.1|2868051|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP050126 (Rhodococcus erythropolis strain KB1 plasmid plas2, complete sequence) position: , mismatch: 6, identity: 0.786

aacctgcgggagaacagggtaatcgggc	CRISPR spacer
ggaatgcgggagaacaaggtaatcggcc	Protospacer
..  ************.********* *

118. spacer 37.1|2868051|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP024940 (Paraburkholderia hospita strain mHSR1 plasmid pmHSR1_P, complete sequence) position: , mismatch: 6, identity: 0.786

aacctgcgggagaacagggtaatcgggc	CRISPR spacer
cgcctgcgagagaacagggtaatgcgcc	Protospacer
 .******.**************  * *

119. spacer 42.1|3996224|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP024940 (Paraburkholderia hospita strain mHSR1 plasmid pmHSR1_P, complete sequence) position: , mismatch: 6, identity: 0.786

aacctgcgagagaacaggggaatcgggc	CRISPR spacer
cgcctgcgagagaacagggtaatgcgcc	Protospacer
 .***************** ***  * *

120. spacer 48.1|4912681|26|NZ_LN831776|CRISPRCasFinder matches to KX961631 (Bacillus phage QCM11, complete genome) position: , mismatch: 6, identity: 0.769

ataaaagattaagatcaaaacacctc	CRISPR spacer
tgaaaagattaagatcaaaacttata	Protospacer
  ******************* . * 

121. spacer 48.1|4912681|26|NZ_LN831776|CRISPRCasFinder matches to NC_049966 (Bacillus phage vB_BthP-Goe4, complete genome) position: , mismatch: 6, identity: 0.769

ataaaagattaagatcaaaacacctc	CRISPR spacer
tgaaaagattaagatcaaaacttata	Protospacer
  ******************* . * 

122. spacer 59.1|5654499|27|NZ_LN831776|CRISPRCasFinder matches to NZ_CP032341 (Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence) position: , mismatch: 6, identity: 0.778

ttttcgggcaagctggccttcgacgac	CRISPR spacer
gacgccggcaagctggccttcgccgac	Protospacer
  . * **************** ****

123. spacer 59.1|5654499|27|NZ_LN831776|CRISPRCasFinder matches to NZ_CP032347 (Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence) position: , mismatch: 6, identity: 0.778

ttttcgggcaagctggccttcgacgac	CRISPR spacer
gacgccggcaagctggccttcgccgac	Protospacer
  . * **************** ****

124. spacer 59.1|5654499|27|NZ_LN831776|CRISPRCasFinder matches to NZ_CP012916 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence) position: , mismatch: 6, identity: 0.778

ttttcgggcaagctggccttcgacgac	CRISPR spacer
gacgccggcaagctggccttcgccgac	Protospacer
  . * **************** ****

125. spacer 70.2|6958084|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP010764 (Phaeobacter inhibens strain P80 plasmid pP80_h, complete sequence) position: , mismatch: 6, identity: 0.786

tcaccgatcacggctgcgccgcgcctaa	CRISPR spacer
tcatcggtcacggctgcgccgcgctgcg	Protospacer
***.**.*****************.  .

126. spacer 70.2|6958084|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP010764 (Phaeobacter inhibens strain P80 plasmid pP80_h, complete sequence) position: , mismatch: 6, identity: 0.786

tcaccgatcacggctgcgccgcgcctaa	CRISPR spacer
tcatcggtcacggctgcgccgcgctgcg	Protospacer
***.**.*****************.  .

127. spacer 70.2|6958084|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP034351 (Streptomyces sp. W1SF4 plasmid p1, complete sequence) position: , mismatch: 6, identity: 0.786

tcaccgatcacggctgcgccgcgcctaa	CRISPR spacer
ccgccgaccacggctgagccgcgcctcc	Protospacer
.*.****.******** *********  

128. spacer 70.2|6958084|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP023408 (Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence) position: , mismatch: 6, identity: 0.786

tcaccgatcacggctgcgccgcgcctaa	CRISPR spacer
tcaccgaccacggccgcgccgcggacga	Protospacer
*******.******.********  ..*

129. spacer 70.2|6958084|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP017105 (Rhizobium gallicum strain IE4872 plasmid pRgalIE4872d, complete sequence) position: , mismatch: 6, identity: 0.786

tcaccgatcacggctgcgccgcgcctaa	CRISPR spacer
gcaccgagcacggctgcgccgagcgtgc	Protospacer
 ****** ************* ** *. 

130. spacer 70.2|6958084|28|NZ_LN831776|CRISPRCasFinder matches to CP006880 (Rhizobium gallicum bv. gallicum R602 plasmid pRgalR602c, complete sequence) position: , mismatch: 6, identity: 0.786

tcaccgatcacggctgcgccgcgcctaa	CRISPR spacer
gcaccgagcacggctgcgccgagcgtgc	Protospacer
 ****** ************* ** *. 

131. spacer 75.1|7578918|27|NZ_LN831776|CRISPRCasFinder matches to NZ_CP054028 (Rhizobium sp. JKLM19E plasmid pPR19E01, complete sequence) position: , mismatch: 6, identity: 0.778

agatactccatacgctgaatgggtccg	CRISPR spacer
tctcgctccattcgctgaatgggtccg	Protospacer
   ..****** ***************

132. spacer 1.1|114349|28|NZ_LN831776|CRISPRCasFinder matches to MN693364 (Marine virus AFVG_25M258, complete genome) position: , mismatch: 7, identity: 0.75

aacctgcggagaacaggagattcgggca	CRISPR spacer
acgtaaaggagaacaggagtttcgggca	Protospacer
*  . . ************ ********

133. spacer 8.1|670877|28|NZ_LN831776|CRISPRCasFinder matches to MN693364 (Marine virus AFVG_25M258, complete genome) position: , mismatch: 7, identity: 0.75

aacctgcggagaacaggagattcgggca	CRISPR spacer
acgtaaaggagaacaggagtttcgggca	Protospacer
*  . . ************ ********

134. spacer 20.1|1558504|28|NZ_LN831776|CRISPRCasFinder matches to AP013820 (Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C15-MedDCM-OCT-S46-C98, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 7, identity: 0.75

aacctgcgaagaatagggtgttcaggta	CRISPR spacer
ttttggcgaagaatagggtgtctaggta	Protospacer
  .. ****************..*****

135. spacer 20.1|1558504|28|NZ_LN831776|CRISPRCasFinder matches to AP014449 (Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C15-MedDCM-OCT-S28-C118, *** SEQUENCING IN PROGRESS ***, 2 ordered pieces) position: , mismatch: 7, identity: 0.75

aacctgcgaagaatagggtgttcaggta	CRISPR spacer
ttttggcgaagaatagggtgtctaggta	Protospacer
  .. ****************..*****

136. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MH153809 (Gordonia phage Sitar, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgacctcgcc	Protospacer
.**********************.**..* ..*

137. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MH976518 (Gordonia phage Stultus, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgacctcgcc	Protospacer
.**********************.**..* ..*

138. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MH976511 (Gordonia phage Gaea, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgacctcgcc	Protospacer
.**********************.**..* ..*

139. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MK937594 (Gordonia phage Galadriel, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgacctcgcc	Protospacer
.**********************.**..* ..*

140. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MN329673 (Gordonia phage Jabberwocky, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgacctcgcc	Protospacer
.**********************.**..* ..*

141. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MT723934 (Gordonia phage Love, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgacctcgcc	Protospacer
.**********************.**..* ..*

142. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MT639640 (Gordonia phage Paries, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgacctcgcc	Protospacer
.**********************.**..* ..*

143. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MK977702 (Gordonia terrae phage McKinley, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgacctcgcc	Protospacer
.**********************.**..* ..*

144. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NC_042108 (Gordonia phage Brandonk123, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgacctcgcc	Protospacer
.**********************.**..* ..*

145. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MH976508 (Gordonia phage Bibwit, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgacctcgcc	Protospacer
.**********************.**..* ..*

146. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NC_042045 (Gordonia phage Lennon, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgacctcgcc	Protospacer
.**********************.**..* ..*

147. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MH976507 (Gordonia phage Ailee, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgacctcgcc	Protospacer
.**********************.**..* ..*

148. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MH651168 (Gordonia phage Ashertheman, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgacctcgcc	Protospacer
.**********************.**..* ..*

149. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MK967396 (Gordonia phage Tangerine, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcacgaggacgacctcgcc	Protospacer
.**********************.**..* ..*

150. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP029455 (Bacillus cereus strain FORC087 plasmid pFORC087.1, complete sequence) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
attttgacgcgatggcatgaggatgatttagct	Protospacer
**. ******* *****.************...

151. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MK937607 (Gordonia phage Zipp, complete genome) position: , mismatch: 7, identity: 0.788

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcatcaggatgatctggcc	Protospacer
.****************. ********.*...*

152. spacer 23.31|1615946|33|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR matches to NC_004768 (Bifidobacterium longum RW041 plasmid pNAC3, complete sequence) position: , mismatch: 7, identity: 0.788

ctggcg-tccctggtggaatacctgaaaggcctg	CRISPR spacer
-gggcgttccctggaggagtacctgaaaggctgc	Protospacer
  **** ******* ***.************.  

153. spacer 23.37|1616340|32|NZ_LN831776|CRT matches to NZ_CP024200 (Thalassospira marina strain CSC3H3 plasmid pCSC3H3, complete sequence) position: , mismatch: 7, identity: 0.781

tcttccccacgttggctttgccaatgtgattg	CRISPR spacer
gctgtttcgcgttggctttgccgatgtgattg	Protospacer
 ** ...*.*************.*********

154. spacer 23.37|1616340|32|NZ_LN831776|CRT matches to NZ_CP042262 (Litoreibacter sp. LN3S51 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.781

tcttccccacgttggctttgccaatgtgattg	CRISPR spacer
cctgacactcgttggctttgccaatgtctttg	Protospacer
.**  * * ******************  ***

155. spacer 30.1|2307535|27|NZ_LN831776|CRISPRCasFinder matches to NZ_CP024200 (Thalassospira marina strain CSC3H3 plasmid pCSC3H3, complete sequence) position: , mismatch: 7, identity: 0.741

tactcaagcatcatgcttctccgcaat	CRISPR spacer
ctatcaagcatcatgcttctccatttt	Protospacer
.  *******************..  *

156. spacer 32.1|2606679|27|NZ_LN831776|CRISPRCasFinder matches to CP000617 (Burkholderia vietnamiensis G4 plasmid pBVIE01, complete sequence) position: , mismatch: 7, identity: 0.741

gaagcgccgaaggctggtttgaccata	CRISPR spacer
tgagcggcgaaggctggtttgacgggt	Protospacer
 .**** **************** .  

157. spacer 32.1|2606679|27|NZ_LN831776|CRISPRCasFinder matches to NZ_CP016452 (Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence) position: , mismatch: 7, identity: 0.741

gaagcgccgaaggctggtttgaccata	CRISPR spacer
aaagcggcgaaggctggtttgatagcg	Protospacer
.***** ***************. ...

158. spacer 33.3|2627427|28|NZ_LN831776|CRISPRCasFinder matches to NZ_AP018282 (Chondrocystis sp. NIES-4102 plasmid plasmid1 DNA, complete genome) position: , mismatch: 7, identity: 0.75

ttctaaaaaagaacaaaatagtgaaaat	CRISPR spacer
catcaaaaaagaccaaaatagtgaaatc	Protospacer
. ..******** ************* .

159. spacer 33.3|2627427|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP037748 (Campylobacter helveticus strain 2013D-9613 plasmid unnamed2, complete sequence) position: , mismatch: 7, identity: 0.75

ttctaaaaaagaacaaaatagtgaaaat	CRISPR spacer
caagaaaaaagaacaaaatattaaaaac	Protospacer
.   **************** *.****.

160. spacer 33.3|2627427|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP020480 (Campylobacter helveticus strain ATCC 51209 plasmid pHELV-2, complete sequence) position: , mismatch: 7, identity: 0.75

ttctaaaaaagaacaaaatagtgaaaat	CRISPR spacer
caagaaaaaagaacaaaatattaaaaac	Protospacer
.   **************** *.****.

161. spacer 33.3|2627427|28|NZ_LN831776|CRISPRCasFinder matches to MN694638 (Marine virus AFVG_250M1093, complete genome) position: , mismatch: 7, identity: 0.75

ttctaaaaaagaacaaaatagtgaaaat	CRISPR spacer
taataaaaaacaacaaaatagtgactgg	Protospacer
*  ******* *************  . 

162. spacer 37.1|2868051|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP049038 (Pseudohalocynthiibacter aestuariivivens strain RR4-35 plasmid pRR4-35_1, complete sequence) position: , mismatch: 7, identity: 0.75

aacctgcgggagaacagggtaatcgggc	CRISPR spacer
ctcatgtgggagaacagggtaatcgatg	Protospacer
  * **.******************.  

163. spacer 37.1|2868051|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP045407 (Roseovarius sp. THAF9 plasmid pTHAF9_c, complete sequence) position: , mismatch: 7, identity: 0.75

aacctgcgggagaacagggtaatcgggc	CRISPR spacer
ctcatgtgggagaacagggtaatcgatg	Protospacer
  * **.******************.  

164. spacer 42.1|3996224|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP021367 (Acidovorax carolinensis strain P4 plasmid pACP4.1, complete sequence) position: , mismatch: 7, identity: 0.75

aacctgcgagagaacaggggaatcgggc	CRISPR spacer
gcgctgcgagagatcagggcaatcggaa	Protospacer
.  ********** ***** ******. 

165. spacer 42.1|3996224|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP021367 (Acidovorax carolinensis strain P4 plasmid pACP4.1, complete sequence) position: , mismatch: 7, identity: 0.75

aacctgcgagagaacaggggaatcgggc	CRISPR spacer
gcgctgcgagagatcagggcaatcggaa	Protospacer
.  ********** ***** ******. 

166. spacer 42.1|3996224|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP021363 (Acidovorax carolinensis strain P3 plasmid pACP3.1, complete sequence) position: , mismatch: 7, identity: 0.75

aacctgcgagagaacaggggaatcgggc	CRISPR spacer
gcgctgcgagagatcagggcaatcggaa	Protospacer
.  ********** ***** ******. 

167. spacer 51.1|5084501|33|NZ_LN831776|CRISPRCasFinder matches to NZ_CP054613 (Paenibacillus cellulosilyticus strain KACC 14175 plasmid unnamed4, complete sequence) position: , mismatch: 7, identity: 0.788

ttcgtac-aaaactggcttcggaagcatacgctt	CRISPR spacer
-acaaacaaaaacttacttcggaagcatacgctc	Protospacer
  *. ** ****** .*****************.

168. spacer 57.1|5507775|30|NZ_LN831776|CRT matches to KX349297 (Cyanophage S-RIM44 isolate W2_10_0709, complete genome) position: , mismatch: 7, identity: 0.767

tggaggtgtagatgcagacgtatttgcaaa	CRISPR spacer
ttcaaatgtagatgcagatgtagttgcaat	Protospacer
*  *..************.*** ****** 

169. spacer 57.1|5507775|30|NZ_LN831776|CRT matches to KU594607 (Cyanophage S-RIM44 isolate W2_07_0710, complete genome) position: , mismatch: 7, identity: 0.767

tggaggtgtagatgcagacgtatttgcaaa	CRISPR spacer
ttcaaatgtagatgcagatgtagttgcaat	Protospacer
*  *..************.*** ****** 

170. spacer 57.1|5507775|30|NZ_LN831776|CRT matches to NC_015288 (Prochlorococcus phage Syn1, complete genome) position: , mismatch: 7, identity: 0.767

tggaggtgtagatgcagacgtatttgcaaa	CRISPR spacer
ttcaaatgtagatgcagatgtagttgcaat	Protospacer
*  *..************.*** ****** 

171. spacer 57.1|5507775|30|NZ_LN831776|CRT matches to KX349295 (Cyanophage S-RIM44 isolate Sn_08_0709, complete genome) position: , mismatch: 7, identity: 0.767

tggaggtgtagatgcagacgtatttgcaaa	CRISPR spacer
ttcaaatgtagatgcagatgtagttgcaat	Protospacer
*  *..************.*** ****** 

172. spacer 57.1|5507775|30|NZ_LN831776|CRT matches to KX349292 (Cyanophage S-RIM44 isolate Np_05_0604, complete genome) position: , mismatch: 7, identity: 0.767

tggaggtgtagatgcagacgtatttgcaaa	CRISPR spacer
ttcaaatgtagatgcagatgtagttgcaat	Protospacer
*  *..************.*** ****** 

173. spacer 59.1|5654499|27|NZ_LN831776|CRISPRCasFinder matches to NZ_LT969519 (Pseudomonas aeruginosa isolate RW109 genome assembly, plasmid: RW109 plasmid 1) position: , mismatch: 7, identity: 0.741

ttttcgggcaagctggccttcgacgac	CRISPR spacer
gccggcggcaagctggcctacgacgac	Protospacer
 ..   ************* *******

174. spacer 60.1|5681511|29|NZ_LN831776|CRISPRCasFinder matches to NZ_CP054145 (Deefgea sp. D17 plasmid unnamed2, complete sequence) position: , mismatch: 7, identity: 0.759

cttctcaaaactcaacaattgagagattt	CRISPR spacer
actctcaaaactcaacacttgaaagttag	Protospacer
 .*************** ****.** *  

175. spacer 62.1|6127671|29|NZ_LN831776|CRISPRCasFinder matches to CP047389 (Agrobacterium sp. CGMCC 11546 plasmid pA) position: , mismatch: 7, identity: 0.759

tgccggagtaccctgccctcgggcagatg	CRISPR spacer
gagccgagtaccctgccctcgcgctgata	Protospacer
 . * **************** ** ***.

176. spacer 63.1|6227005|29|NZ_LN831776|CRISPRCasFinder matches to NZ_CP015065 (Mesorhizobium ciceri biovar biserrulae strain WSM1284 plasmid pMc1284, complete sequence) position: , mismatch: 7, identity: 0.759

tgccgaagtaccctaccctcgggcagata	CRISPR spacer
cgccgaaataccccaccctcgggcgagga	Protospacer
.******.*****.**********... *

177. spacer 64.1|6490668|28|NZ_LN831776|CRISPRCasFinder matches to CP053324 (Salmonella enterica subsp. salamae serovar 40:c:e,n,z15 strain 2013K-0524 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.75

agtttgggtaacgcagggctatcgagca	CRISPR spacer
atcctggctaacgcagggctatcgacag	Protospacer
* ..*** *****************  .

178. spacer 69.1|6944723|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP043831 (Bacillus sp. BS98 plasmid unnamed1) position: , mismatch: 7, identity: 0.75

aaacctcacaattgttgattttagggag	CRISPR spacer
aatccgcacaattgttgattttactcgt	Protospacer
** ** *****************   . 

179. spacer 70.2|6958084|28|NZ_LN831776|CRISPRCasFinder matches to NZ_LR594668 (Variovorax sp. SRS16 plasmid 3) position: , mismatch: 7, identity: 0.75

tcaccgatcacggctgcgccgcgcctaa	CRISPR spacer
ccgccgatcacggcagcgccgcgctgtg	Protospacer
.*.*********** *********.  .

180. spacer 70.2|6958084|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP012748 (Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.75

tcaccgatcacggctgcgccgcgcctaa	CRISPR spacer
cgtgcgatcgctgctgcgccgcgcctat	Protospacer
.   *****.* *************** 

181. spacer 19.1|1507993|35|NZ_LN831776|CRISPRCasFinder matches to NZ_CP054613 (Paenibacillus cellulosilyticus strain KACC 14175 plasmid unnamed4, complete sequence) position: , mismatch: 8, identity: 0.771

tgcttcgtac-aaaacttacttcgtaagcataagct	CRISPR spacer
-cccacaaacaaaaacttacttcggaagcatacgct	Protospacer
  *. *. ** ************* ******* ***

182. spacer 21.6|1593117|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MT374854 (Yersinia phage vB_YpM_6, complete genome) position: , mismatch: 8, identity: 0.771

cgaaactgccggaagtcgtgaaacaaatgtccaag-----	CRISPR spacer
aaaaactgccggaagtggtgaaacaaa-----aagggcgc	Protospacer
 .************** **********     ***     

183. spacer 21.6|1593117|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MT374853 (Yersinia phage vB_YpM_5, complete genome) position: , mismatch: 8, identity: 0.771

cgaaactgccggaagtcgtgaaacaaatgtccaag-----	CRISPR spacer
aaaaactgccggaagtggtgaaacaaa-----aagggcgc	Protospacer
 .************** **********     ***     

184. spacer 22.25|1605039|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP036456 (Streptomonospora sp. M2 plasmid phiM2, complete sequence) position: , mismatch: 8, identity: 0.771

gaccttccaggcgccgccgtctgcctcgatcaggg	CRISPR spacer
cacgtcaccggcgccgccgcctgcctcgaccagga	Protospacer
 ** *. * **********.*********.****.

185. spacer 23.4|1614158|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MH976512 (Gordonia phage Geodirt, complete genome) position: , mismatch: 8, identity: 0.758

atcatgacgcgctggcacgaggatgatttaatc	CRISPR spacer
gtcatgacgcgctggcatgaggacgacctcgcc	Protospacer
.****************.*****.**..* ..*

186. spacer 23.16|1614957|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_AP017384 (Moraxella osloensis strain KMC41 plasmid pMOSL3, complete sequence) position: , mismatch: 8, identity: 0.765

agcagcagtctaatcatatagatttagagtatcc	CRISPR spacer
atcagccgtctaatcataaagatttacatgctca	Protospacer
* **** *********** ******* *   ** 

187. spacer 23.17|1615023|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NC_013155 (Lactococcus phage CB13, complete genome) position: , mismatch: 8, identity: 0.765

tcagtttccgcagcctttgcattttcggctttat	CRISPR spacer
ttatctttttcagcctttgccttttccgctttat	Protospacer
*.* .**.. ********** ***** *******

188. spacer 23.17|1615023|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to HM029250 (Lactococcus phage 949, complete genome) position: , mismatch: 8, identity: 0.765

tcagtttccgcagcctttgcattttcggctttat	CRISPR spacer
ttatctttttcagcctttgccttttccgctttat	Protospacer
*.* .**.. ********** ***** *******

189. spacer 23.17|1615023|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to KC522412 (Lactococcus phage CaseusJM1, complete genome) position: , mismatch: 8, identity: 0.765

tcagtttccgcagcctttgcattttcggctttat	CRISPR spacer
ttatctttttcagcctttgccttttccgctttat	Protospacer
*.* .**.. ********** ***** *******

190. spacer 23.28|1615749|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR matches to MG065650 (UNVERIFIED: Campylobacter phage B15, complete genome) position: , mismatch: 8, identity: 0.765

ttgtttgcaatttaattaatgaatacttatgtat	CRISPR spacer
gtgtttgcaaattacttaatgaataatgttgggt	Protospacer
 ********* *** ********** *  ** .*

191. spacer 23.28|1615749|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR matches to LR746137 (Escherichia phage vB_EcoM_UP17 genome assembly, chromosome: 1) position: , mismatch: 8, identity: 0.765

ttgtttgcaatttaattaatgaatacttatgtat	CRISPR spacer
gtgtttgcaaattacttaatgaataatgttgggt	Protospacer
 ********* *** ********** *  ** .*

192. spacer 24.8|1620370|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR matches to EU717894 (Xanthomonas phage phiL7, complete genome) position: , mismatch: 8, identity: 0.765

taacgccgggtgcagcaacacgctgcgggtacat	CRISPR spacer
ttacaccgggtgcagcaacacgcagcgtggtggt	Protospacer
* **.****************** *** *   .*

193. spacer 27.1|2153720|29|NZ_LN831776|CRISPRCasFinder matches to NZ_CP015065 (Mesorhizobium ciceri biovar biserrulae strain WSM1284 plasmid pMc1284, complete sequence) position: , mismatch: 8, identity: 0.724

catctgcccgagggtagggtacttcggca	CRISPR spacer
tcctcgcccgagggtggggtatttcggcg	Protospacer
. ...**********.*****.******.

194. spacer 33.1|2627304|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP033935 (Chryseobacterium balustinum strain KC_1863 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.714

ccagcaaaatatgcagaaaaccgtgagt	CRISPR spacer
tttaaaaaatatgcagaaaaccgcgatg	Protospacer
.. . ******************.**  

195. spacer 43.1|4328542|29|NZ_LN831776|CRISPRCasFinder matches to NZ_CP015065 (Mesorhizobium ciceri biovar biserrulae strain WSM1284 plasmid pMc1284, complete sequence) position: , mismatch: 8, identity: 0.724

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
cgccgaaataccccaccctcgggcgagga	Protospacer
.******.*****.**********... .

196. spacer 57.2|5507823|30|NZ_LN831776|CRT matches to KU599879 (Flavobacterium phage Fpv3, complete genome) position: , mismatch: 8, identity: 0.733

tgcagacataagtgcagatataggtgcaga	CRISPR spacer
gagtaaaataagtgcagagatagttgcaga	Protospacer
 .  .* *********** **** ******

197. spacer 57.2|5507823|30|NZ_LN831776|CRT matches to MK764441 (Flavobacterium phage FPSV-F12, complete genome) position: , mismatch: 8, identity: 0.733

tgcagacataagtgcagatataggtgcaga	CRISPR spacer
gagtaaaataagtgcagagatagttgcaga	Protospacer
 .  .* *********** **** ******

198. spacer 57.2|5507823|30|NZ_LN831776|CRT matches to KU599886 (Flavobacterium phage Fpv20, complete genome) position: , mismatch: 8, identity: 0.733

tgcagacataagtgcagatataggtgcaga	CRISPR spacer
gagtaaaataagtgcagagatagttgcaga	Protospacer
 .  .* *********** **** ******

199. spacer 57.2|5507823|30|NZ_LN831776|CRT matches to NC_031931 (Flavobacterium phage Fpv2, complete genome) position: , mismatch: 8, identity: 0.733

tgcagacataagtgcagatataggtgcaga	CRISPR spacer
gagtaaaataagtgcagagatagttgcaga	Protospacer
 .  .* *********** **** ******

200. spacer 57.2|5507823|30|NZ_LN831776|CRT matches to KT876726 (Flavobacterium phage FpV21, complete genome) position: , mismatch: 8, identity: 0.733

tgcagacataagtgcagatataggtgcaga	CRISPR spacer
gagtaaaataagtgcagagatagttgcaga	Protospacer
 .  .* *********** **** ******

201. spacer 57.2|5507823|30|NZ_LN831776|CRT matches to KT876724 (Flavobacterium phage FpV4, complete genome) position: , mismatch: 8, identity: 0.733

tgcagacataagtgcagatataggtgcaga	CRISPR spacer
gagtaaaataagtgcagagatagttgcaga	Protospacer
 .  .* *********** **** ******

202. spacer 57.2|5507823|30|NZ_LN831776|CRT matches to KU599877 (Flavobacterium phage Fpv1, complete genome) position: , mismatch: 8, identity: 0.733

tgcagacataagtgcagatataggtgcaga	CRISPR spacer
gagtaaaataagtgcagagatagttgcaga	Protospacer
 .  .* *********** **** ******

203. spacer 69.1|6944723|28|NZ_LN831776|CRISPRCasFinder matches to MK047640 (Phage NV18, complete genome) position: , mismatch: 8, identity: 0.714

aaacctcacaattgttgattttagggag	CRISPR spacer
caacctcacaattgtttattttttatca	Protospacer
 *************** *****  .  .

204. spacer 70.2|6958084|28|NZ_LN831776|CRISPRCasFinder matches to NZ_CP014169 (Sphingomonas panacis strain DCY99 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.714

tcaccgatcacggctgcgccgcgcctaa	CRISPR spacer
aaggggattacggctgcgccgcgcctct	Protospacer
  .  ***.*****************  

205. spacer 77.1|7629925|29|NZ_LN831776|CRISPRCasFinder matches to NZ_CP015065 (Mesorhizobium ciceri biovar biserrulae strain WSM1284 plasmid pMc1284, complete sequence) position: , mismatch: 8, identity: 0.724

tgccgaagtaccctaccctcgggcagatg	CRISPR spacer
cgccgaaataccccaccctcgggcgagga	Protospacer
.******.*****.**********... .

206. spacer 21.11|1593453|36|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021876 (Enterococcus wangshanyuanii strain MN05 plasmid unnamed3) position: , mismatch: 9, identity: 0.75

actgaaacagtcaaagaactcaaagaggccgtcaag	CRISPR spacer
actcaaatagtcaaagaactcaaagaaaaagataat	Protospacer
*** ***.******************..  * .** 

207. spacer 21.15|1593720|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP034143 (Marinobacter sp. NP-4(2019) plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.735

cataagatcatccaggatcttgtcctgcttattc	CRISPR spacer
cgggcgatcattcaggatcttgacctgcttgccc	Protospacer
*. . ******.********** *******...*

208. spacer 21.15|1593720|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to JX100810 (Caulobacter phage CcrColossus, complete genome) position: , mismatch: 9, identity: 0.735

cataagatcatccaggatcttgtcctgcttattc-----	CRISPR spacer
gataagatcatcctcgatcttgtcc-----atttccgga	Protospacer
 ************  **********     ***.     

209. spacer 21.23|1594250|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP015325 (Bacillus filamentosus strain Hbe603 plasmid pBEH3, complete sequence) position: , mismatch: 9, identity: 0.735

caactactacaaaaccccactcgaacaatggatt	CRISPR spacer
aatcccatttaaaaacccattcgaacaatggatt	Protospacer
 * *.  * .**** ****.**************

210. spacer 21.25|1594383|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NC_010625 (Paraburkholderia phymatum STM815 plasmid pBPHY01, complete sequence) position: , mismatch: 9, identity: 0.735

cgggtgatcggaggagacgaataatggcagtaga	CRISPR spacer
cgggttatcggaggagacgaaaaatgaaaaggat	Protospacer
***** *************** ****. *. .. 

211. spacer 22.2|1603508|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP043613 (Lactobacillus buchneri strain MGB0786 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.735

accaatcttgataaagatcagaaatacaaacttg	CRISPR spacer
gaccaggttgataaagatttgaaatacaaactgc	Protospacer
. * *  ***********. ************  

212. spacer 22.21|1604773|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP016617 (Microvirga ossetica strain V5/3m plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.743

caccagggacgccaggaaggccgtccgcacctggg	CRISPR spacer
tgcgcgagatgccaggaaggccgtccgaacctatg	Protospacer
..*  *.**.***************** ****. *

213. spacer 22.25|1605039|35|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to JQ680374 (Unidentified phage clone 2209_scaffold441 genomic sequence) position: , mismatch: 9, identity: 0.743

gaccttccaggcgccgccgtctgcctcgatcaggg	CRISPR spacer
cagtttccagacgccgccgtcagcctcgaagaagc	Protospacer
 * .******.********** *******  *.* 

214. spacer 23.28|1615749|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR matches to MN850571 (Escherichia phage nepoznato, complete genome) position: , mismatch: 9, identity: 0.735

ttgtttgcaatttaattaatgaatacttatgtat	CRISPR spacer
gtgtttgcaaattacttaatgaataatgtcgggt	Protospacer
 ********* *** ********** *  .* .*

215. spacer 23.28|1615749|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR matches to MH051333 (Escherichia phage vB_EcoM-Ro121c4YLVW, complete genome) position: , mismatch: 9, identity: 0.735

ttgtttgcaatttaattaatgaatacttatgtat	CRISPR spacer
gtgtttgcaaattacttaatgaataatgtcgggt	Protospacer
 ********* *** ********** *  .* .*

216. spacer 23.28|1615749|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR matches to NC_047776 (Escherichia phage ESCO5, complete genome) position: , mismatch: 9, identity: 0.735

ttgtttgcaatttaattaatgaatacttatgtat	CRISPR spacer
gtgtttgcaaattacttaatgaataatgtcgggt	Protospacer
 ********* *** ********** *  .* .*

217. spacer 23.28|1615749|34|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR matches to NC_019521 (Sphingomonas phage PAU, complete genome) position: , mismatch: 9, identity: 0.735

ttgtttgcaatttaattaatgaatacttatgtat	CRISPR spacer
ttcagagatattaaactaatgaatacttatgtaa	Protospacer
**    *  *** **.***************** 

218. spacer 23.31|1615946|33|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR matches to MF153391 (Escherichia phage ST2, complete genome) position: , mismatch: 9, identity: 0.727

ctggcgtccctggtggaatacctgaaaggcctg	CRISPR spacer
gacgaagacctggtggaatacctggaacgcctg	Protospacer
   * .  ****************.** *****

219. spacer 23.35|1616209|33|NZ_LN831776|CRISPRCasFinder,CRT,PILER-CR matches to NC_009760 (Bacillus phage 0305phi8-36, complete genome) position: , mismatch: 9, identity: 0.727

atcctgacaggcatcaaggataagaagttgcaa	CRISPR spacer
ctagagactggcatcaagtataagaagttcgac	Protospacer
 *   *** ********* **********  * 

220. spacer 24.27|1621634|32|NZ_LN831776|CRT matches to NZ_CP034431 (Bradyrhizobium sp. LCT2 plasmid pLCT2, complete sequence) position: , mismatch: 9, identity: 0.719

------caaggaccgggaaggaaaagccgtcgcggaag	CRISPR spacer
gcttgtagaggac------ggaaaagccgtcgcggcag	Protospacer
       .*****      **************** **

221. spacer 21.1|1592787|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to KU878088 (Bacillus phage AR9, complete genome) position: , mismatch: 10, identity: 0.706

ttttggtttttaaagatggaagagttgtagagaa	CRISPR spacer
aaacacgttttaaagatggaagagctgaagagga	Protospacer
   ..  *****************.** ****.*

222. spacer 21.1|1592787|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MF360957 (Bacillus virus PBS1, complete genome) position: , mismatch: 10, identity: 0.706

ttttggtttttaaagatggaagagttgtagagaa	CRISPR spacer
aaacacgttttaaagatggaagagctgaagagga	Protospacer
   ..  *****************.** ****.*

223. spacer 22.8|1603905|33|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LT984809 (Cupriavidus taiwanensis isolate Cupriavidus taiwanensis STM 8555 plasmid I, complete sequence) position: , mismatch: 10, identity: 0.697

ctgtatactctcgaacaaaattattgatgctat	CRISPR spacer
aggtatactgtcgaacaaaattaatggaagact	Protospacer
  ******* ************* **. .   *

224. spacer 23.17|1615023|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP039845 (Acetobacter pasteurianus strain CICC 22518 plasmid pAP22518-1, complete sequence) position: , mismatch: 10, identity: 0.706

tcagtttccgcagcctttgcattttcggctttat	CRISPR spacer
gccatggccgcagccttttcattttcgacttctg	Protospacer
 * .*  *********** ********.***.  

225. spacer 24.6|1620236|34|NZ_LN831776|CRISPRCasFinder,CRT matches to NZ_CP028970 (Aminobacter sp. MSH1 plasmid pUSP2, complete sequence) position: , mismatch: 10, identity: 0.706

atcgtcagcagcatccacaatcgtagatggtctt	CRISPR spacer
atcgtcatcggcatccacaatcgttcaccatggg	Protospacer
******* *.**************  *. .*   

226. spacer 21.3|1592919|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP013615 (Clostridium perfringens strain JP838 plasmid pJFP838A, complete sequence) position: , mismatch: 11, identity: 0.676

agggccttatccattatgactacatcatattttc	CRISPR spacer
gaattagtatcaattattactacatcatattctt	Protospacer
... .  **** ***** *************.*.

227. spacer 21.25|1594383|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP038238 (Leisingera sp. NJS201 plasmid unnamed4, complete sequence) position: , mismatch: 11, identity: 0.676

cgggtgatcggaggagacgaataatggcagtaga	CRISPR spacer
gccgtgatcggaggagacgtgtaatggataccgg	Protospacer
   **************** .******  .. *.

228. spacer 21.25|1594383|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP035421 (Leisingera sp. NJS204 plasmid unnamed4, complete sequence) position: , mismatch: 11, identity: 0.676

cgggtgatcggaggagacgaataatggcagtaga	CRISPR spacer
gccgtgatcggaggagacgtgtaatggacaccgg	Protospacer
   **************** .******  .. *.

229. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_KX710093 (Leclercia adecarboxylata strain pP10164 plasmid pP10164-2, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

230. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_KY270852 (Enterobacter cloacae strain T5282 plasmid pT5282-mphA, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

231. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_KY270851 (Citrobacter freundii strain 112298 plasmid p112298-catA, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

232. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LN830952 (Enterobacter sp. 247 strain 247 BMC plasmid pEB247, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

233. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP028537 (Enterobacter hormaechei strain SCEH020042 plasmid pQnrB4_020042, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

234. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP048350 (Raoultella ornithinolytica strain 23 plasmid p23_A-OXA140, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

235. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP044256 (Salmonella enterica strain CFSAN096147 plasmid pCFSAN096147, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

236. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP035634 (Enterobacter cloacae strain EN3600 plasmid unnamed2, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

237. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP042506 (Leclercia adecarboxylata strain E1 plasmid pE1_001, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

238. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MT077884 (Escherichia coli plasmid p33, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

239. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MT077886 (Escherichia coli plasmid p39, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

240. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MN423361 (Leclercia sp. strain 1106151 plasmid p1106151-mcr, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

241. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP025277 (Salmonella enterica subsp. enterica strain USDA-ARS-USMARC-60984 plasmid pSJO-60984, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

242. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MH909331 (Leclercia adecarboxylata plasmid p707804-NDM, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

243. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP008825 (UNVERIFIED_ORG: Enterobacter cloacae ECNIH2 plasmid pKPC-272, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

244. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP022696 (Citrobacter farmeri strain AUSMDU00008141 plasmid pAUSMDU8141-1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

245. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP052871 (Enterobacter cloacae strain 3849 plasmid p3846_IncHI2_mcr, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

246. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to CP049311 (Salmonella enterica subsp. enterica serovar Heidelberg strain CVM N53023 plasmid pN53023, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

247. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LT991958 (Enterobacter cloacae complex sp. isolate C45 plasmid pC45-VIM4) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

248. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP043855 (Enterobacter hormaechei strain EB_P6_L3_02.19 plasmid unnamed2, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

249. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP044215 (Klebsiella aerogenes strain KA_P10_L5_03.19 plasmid pIMPIncH12_334kb, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

250. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to CP049309 (Salmonella enterica subsp. enterica serovar Johannesburg strain CVM N58011 plasmid p58011, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

251. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NC_010870 (Klebsiella pneumoniae plasmid pK29, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

252. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP024813 (Enterobacter sp. CRENT-193 plasmid pCRENT-193_1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

253. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to CP049307 (Salmonella enterica subsp. enterica serovar Heidelberg strain CVM N58631 plasmid p58631, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

254. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP042494 (Leclercia adecarboxylata strain E61 plasmid pE61_001, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

255. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP040696 (Citrobacter freundii strain R47 plasmid pR47-309, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

256. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP042552 (Enterobacter hormaechei strain C45 plasmid pC45_001, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

257. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP039271 (Salmonella enterica subsp. enterica serovar Senftenberg str. CFSAN004025 plasmid pCFSAN004025.1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

258. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP016526 (Salmonella enterica subsp. enterica serovar Heidelberg strain 09-036813-1A plasmid p09-036813-1A_261, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

259. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to CP050163 (Escherichia coli plasmid Carbapenemase(KPC-2)_IncHI2, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

260. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP041734 (Enterobacter hormaechei subsp. steigerwaltii strain ME-1 plasmid pME-1a, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

261. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MK933279 (Enterobacter hormaechei strain SCNJ07 plasmid pMCR-SCNJ07, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

262. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to LC532224 (Enterobacter hormaechei subsp. xiangfangensis A2483 plasmid pA2483mcr-9 DNA, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

263. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to LC532226 (Enterobacter hormaechei subsp. xiangfangensis A2504 plasmid pA2504mcr-9 DNA, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

264. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NC_005211 (Serratia marcescens plasmid R478, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

265. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP026661 (Salmonella enterica subsp. enterica strain 15-SA01028 plasmid pSE15-SA01028, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

266. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to LN794248 (Salmonella enterica subsp. enterica serovar Typhimurium plasmid incHI2, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

267. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP029248 (Enterobacter hormaechei subsp. xiangfangensis strain OSUVMCKPC4-2 plasmid pOSUEC_D, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

268. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP043927 (Klebsiella quasipneumoniae subsp. quasipneumoniae strain M17277 plasmid p17277A_477, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

269. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP031102 (Leclercia sp. W17 plasmid pW17-1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

270. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP012170 (Enterobacter hormaechei subsp. steigerwaltii strain 34977 plasmid p34977-263.138kb, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

271. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to LC542971 (Escherichia coli IOMTU413 plasmid pIOMTU413 DNA, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

272. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to LC542972 (Escherichia coli IOMTU792 plasmid pIOMTU792 DNA, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

273. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to CP051274 (Salmonella enterica subsp. enterica serovar Worthington strain OLF-FSR1_WB_Partridge_SW-37 plasmid pSW37-267109, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

274. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NC_024983 (Salmonella enterica subsp. enterica serovar Typhimurium plasmid pSTm-A54650, strain A54560, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

275. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to CP051271 (Salmonella enterica subsp. enterica serovar Worthington strain OLF-FSR1_WB_Quail_SW-70 plasmid pSW37-267106, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

276. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP013215 (Klebsiella pneumoniae subsp. pneumoniae strain H11 plasmid pH11, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

277. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021463 (Salmonella enterica subsp. enterica serovar Typhimurium strain UGA14 plasmid pUGA14_1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

278. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NC_012556 (Enterobacter cloacae plasmid pEC-IMPQ, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

279. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NC_012555 (Enterobacter cloacae plasmid pEC-IMP, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

280. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP042579 (Enterobacter kobei strain C16 plasmid pC16_001, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

281. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP049193 (Enterobacter hormaechei strain Y2152 plasmid pIHI2-2152, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

282. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP051135 (Enterobacter hormaechei strain AMS-38 plasmid pAMS-38c, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

283. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP032842 (Enterobacter hormaechei strain C15117 plasmid pSPRC-Echo1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

284. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP042525 (Citrobacter freundii strain E11 plasmid pE11_001, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

285. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LT991955 (Enterobacter hormaechei subsp. steigerwaltii isolate C309 plasmid pC309-VIM4) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

286. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP022533 (Enterobacter hormaechei strain MS7884A plasmid pMS7884A, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

287. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP038659 (Citrobacter freundii strain 680 plasmid p680_1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

288. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP029717 (UNVERIFIED_ORG: Enterobacter cloacae strain AR_0154 plasmid unnamed4, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

289. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP024910 (Enterobacter hormaechei subsp. xiangfangensis strain OSUKPC4_L plasmid pOSUKPC4, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

290. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to MN937241 (Enterobacter cloacae strain BSI034 plasmid pBSI034-MCR9, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

291. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP042489 (Enterobacter hormaechei strain C15 plasmid pC15_001, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

292. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_MN540571 (Escherichia coli strain E.coli4feg plasmid pIV_IncHI2_CTX_M_15, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

293. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP033103 (Enterobacter hormaechei strain L51 plasmid pEHZJ1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

294. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_MH829594 (Enterobacter cloacae strain EC62 plasmid pIMP-4-EC62, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

295. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_MK736669 (Enterobacter cloacae strain EclC2185 plasmid pEclC2185CTXM15, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

296. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LC511997 (Enterobacter hormaechei subsp. xiangfangensis strain MY460 plasmid pMY460-rmtE, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

297. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_MF344580 (Enterobacter cloacae strain 30860 plasmid p30860-HI2, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

298. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_MF344581 (Enterobacter cloacae strain 13E573 plasmid p13E573-HI2, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

299. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_MF344583 (Enterobacter cloacae strain N1863 plasmid pN1863-HI2, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

300. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_KY863418 (Enterobacter asburiae strain AMA 497 plasmid pOXA436, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

301. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_KY978628 (Cronobacter sakazakii strain 505108 plasmid p505108-MDR, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

302. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_MF788071 (Raoultella ornithinolytica strain 23141 plasmid p23141-3, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

303. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP031724 (Enterobacter hormaechei strain WCHEH020038 plasmid pCTXM9_020038, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

304. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP053191 (Enterobacter hormaechei strain EGYMCRVIM plasmid pMS-37a, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

305. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_KX810825 (Salmonella enterica subsp. enterica serovar Typhimurium strain MU1 plasmid pIMP4-SEM1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

306. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_KP975077 (Enterobacter cloacae strain MRSN17626 plasmid pMRVIM0813, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

307. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP028197 (Salmonella enterica subsp. enterica serovar Concord strain CFSAN018747 plasmid pGMI14-002_1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

308. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP011601 (Phytobacter ursingii strain CAV1151 plasmid pCAV1151-296, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

309. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP028975 (Cronobacter sakazakii strain GZcsf-1 plasmid pGW1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

310. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP019559 (Escherichia coli strain KSC207 plasmid pMRGN207, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

311. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP048293 (Escherichia coli strain CVM N18EC0432 plasmid pN18EC0432-1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

312. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP020529 (Enterobacter cloacae strain 174 plasmid unnamed1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

313. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP031567 (Enterobacter hormaechei strain 2013_1a plasmid pIncHI2-1301491, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

314. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP040888 (Leclercia adecarboxylata strain Z96-1 plasmid pZ96-1_1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

315. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP042616 (Escherichia coli strain NCYU-26-73 plasmid pNCYU-26-73-1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

316. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP029037 (Salmonella enterica subsp. enterica serovar Senftenberg str. 361154004 plasmid unnamed, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

317. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP030186 (Salmonella enterica strain SA20094620 plasmid pSA20094620.1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

318. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP023570 (Enterobacter hormaechei strain BW plasmid unnamed2, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

319. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NC_021845 (Salmonella enterica subsp. enterica serovar Cubana str. CFSAN002050 plasmid unnamed, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

320. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP027144 (Enterobacter hormaechei subsp. hoffmannii strain AR_0365 plasmid unnamed1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

321. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP049189 (Enterobacter hormaechei strain Y323 plasmid pIHI2-323, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

322. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_AP018352 (Enterobacter hormaechei strain TUM11043 plasmid pMTY11043_IncHI2, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

323. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP038654 (Citrobacter freundii strain 154 plasmid p154_1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

324. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP038657 (Citrobacter freundii strain 565 plasmid p565_1, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

325. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP044051 (Klebsiella variicola strain FDAARGOS_627 plasmid unnamed2, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

326. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_MH105051 (Salmonella enterica subsp. enterica serovar Lomita strain SL131 plasmid pSL131_IncHI2, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

327. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP049047 (Enterobacter hormaechei strain Y233 plasmid pIHI2-233, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

328. spacer 22.24|1604973|34|NZ_LN831776|PILER-CR,CRISPRCasFinder,CRT matches to NZ_MG878867 (Escherichia coli strain Ec21617 plasmid pEc21617-310, complete sequence) position: , mismatch: 11, identity: 0.676

aggttgtcggtgacgttacggtcaaagatgactt	CRISPR spacer
gggttatcggtgacgttacgggcaatattcctcg	Protospacer
.****.*************** *** . *  .. 

329. spacer 24.27|1621634|32|NZ_LN831776|CRT matches to NZ_CP015237 (Rhodococcus fascians D188 plasmid unnamed2, complete sequence) position: , mismatch: 11, identity: 0.656

caaggaccgggaaggaaaagccgtcgcggaag	CRISPR spacer
gcgggaccgggaaggaaattccgtcggcccgc	Protospacer
  .***************  ******    . 

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	191776 : 225794	39	Clostridium_phage(40.74%)	capsid,terminase	NA
DBSCAN-SWA_2	879985 : 891647	9	Mollivirus(25.0%)	NA	NA
DBSCAN-SWA_3	2879522 : 2889953	9	Bacillus_phage(66.67%)	NA	NA
DBSCAN-SWA_4	4939412 : 4961489	17	Cyanophage(50.0%)	plate,tail	NA
DBSCAN-SWA_5	5247547 : 5256690	10	Staphylococcus_phage(57.14%)	NA	NA
DBSCAN-SWA_6	7070941 : 7123388	57	Bacteriophage(25.0%)	tail,portal,tRNA,plate,holin	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_LN831776|191776:225794|DBSCAN-SWA
GTTGATAACACAGGAACAATTACTGGATTTTATGCGGGAGACCGCTTATAAGCCGCTCACTTATGACGAACTGGTGAGTCATTTCGCATTAGAGGACAGCGAGTCGTTCAAAGCGTTTGAGGAATTGCTGCTTGCACTTGAGCAGGATGGAAGAATGATACTGACCCGGAATGCCCGCTACGGGGTACCGGAACGGATGGATTTGGTGCGCGGACGTGTACAGGCTCATGCGAAGGGGTTTGCTTTTCTGATTCCCGATGACCGCGATCATCCTGATATTTATATGAATGCCAATGATCTGAAGGGTGCGATGAACGGTGATATCGTGCTGGTGCGCATTACCTCGCGAAGCCCGTCCGGCGGGCGTATGGAAGGCGAAGTTGTGCGGATCGTTAAAAGAGGGGTGCTGCAGACTGTAGGTGTGTTCCAAAGCCTGGAGAACTATGGTTTTGTGCTGCCTGATGATAAGCGGATTAACCGGGATATTTTTATTCCAAAGCAATCCTTCAAGGGTGCAGTTGACGGGGAAAAAGTCGTTGTCCGCATTGTAAATTACCCGGAAGGCCGGGCTGCGGCAGAGGGGGAAATCATTGAGATCCTGGGCCATAAAGATGACCCGGGTGTGGATATTCTGTCGGTGATCCGGAAGCATCAGCTCCCGGAGGCTTTTCCGGCTGAAGTGATGCGTGAAGCGGAGCAGGCTCCTGATTCCATTACGGAGGAAGAAATTATCCAGCAGGGCCGCCGCGATCTGCGCGGGCTGAACATTGTCACCATCGACGGTGCGGACGCCAAGGATCTGGATGATGCCGTGAATGTATCGCGTCTGGAGAACGGCCACTACAAGCTGGGCGTGCATATTGCGGACGTCGGTTATTATGTGCGTGAAGGGTCTGAGCTGGATAAGGAAGCTTTTGACCGCGGGTGCAGCGTGTATCTGGTGGACCGGGTTATCCCCATGCTGCCGCATCGTTTGTCGAACGGCATCTGCAGCTTGAATCCCAAGGTGGACCGGCTAACGATGTCCTGTGAGATGGAATTCGACGAGCATATGAAGGTCGTGAAGCATGATGTCTTTACGAGCGTTATCCGTACGAAGGAAAGAATGACCTACTCGGATGTCCGCAAAATCGTTGAAGACGAAGATCCCGAGCTGCTGGAGCGTTATAGTCCACTGATTGAGGATTTCCGCCTGATGAAAGAGCTGGCGATGAAGCTGCGTGGTGCGCGGATGCGCCGAGGTGCAGTTGATTTCGACTTCGAAGAGAGCAAGATTATCGTCGATGAGAACGGCAAGGCGATAGATATCGTGAAACGCGAGCGTTCCGTGGCTGAGCAGATTATCGAGGAGTTCATGCTGGCGGCGAACGAAACGGTTGCAGAGCATTTCCACTGGCTGAAGGTGCCGTTCCTGTACCGGATTCACGAAGATCCGGACCCGGAGAAGCTGCAGAACTTCATGGCTTTTGCGGCGAACTTTGGCTATCATGTCAAAGGCCGGGGCAATTCGGTGCATCCGCGCGCGCTGCAGGATCTGCTGGAGCAGATTCAGGGGACGAAGGAACAGACCGTCATCAGTACCATGATGCTGCGCTCCATGAAGCAGGCGAAGTATGATGCTGAGAGCACAGGCCACTTCGGGCTGGCTGCGGAATTTTATTCCCATTTCACCTCGCCGATCCGGCGTTATCCCGACCTTGTGATTCACCGTGTCATGCGGGAGGTTATTGAGAACGGCGGAGCGCTGACGGAGAAACGCCATGAATATCTCGCCAGCCGGATGCCGGAGATCGCGCAGCAGTCCTCGGAACGCGAGCGTGTGGCGGTAGAGGCTGAACGGGATACGGAGCAGCTCAAGAAGGCTGAGTTCATGCAGGACAAGGTTGGCGAGGAATTCGACGCCATGGTCAGCAGCGTGACCAGCTTCGGGATGTTCATCGAGCTGGAAAATACCGTCGAAGGCTTAATCCGCCTCAGCGCGCTGAGCGATGATTATTACCACTTCGACGAAGCCCATATGGCGCTCATTGGCGAGCGCACCTCGAAGGTGTTCCGCATTGGCGACGAGGTGAAGATCCGTGTCGCCAAGGTCAACATGGACGACCATACGATTGACTTTGAGCTGGTCGACATGAAGCCGCGCGCGGCAGGTGAACACCGCAGCTTCGGCGGGCGTGGAGGCAAGGGTGGCCGTGCTGGCGGCGGCTTCGCCAAGCCGTTCGGCAGCAAAGCCGGCGGCAAGGGCCGCGCCGGCGGGAAAGGCAAGCCCGGCAGCGCAGCGGGCCGGGGGAAGGCCGGCGGCGCTGCACACGCCGGCAAGGGCAAGTCCGGCGCGGCAGCACGCGCCGGAGAAGCGCCCCGCGCAGCGGAGGAAGCCAGCGGCGGTGCGCCGGCTGGCGGCCGCGGCAAGCGCGGGGGCGGCGGCCCGGCAGAGGCAGCGCGCCGGGCCTTCGCGGCCGTGAACCGCGGCGAGGCTGGCGGTGCCGGCACGCCGCGGGAGCGGGACCGCAGCGGCGGGCGTGGCCGCGGCGGTGAGGCCGGAGGCAGTGCCGGGGGACGCGGCATCAGCTTCGGCTTCGGCTCCGGCAAGGGCGGCTATGGCGCCCCTGCCGGCGAGCAGATCAGCGAGCTGCGCGGCGTGGACGCCAGCACGCGGTTCCGCAGCCGCGAGGATCTCGGCAGCGGGGCAGCGGCCAACGGCGGCGGAGGCAAGAGCCGCCGCAAAAAGAATAAAAAGGGCGGCGTCTTCATCAGCCCTTCCGTAACGCCGGGCAACGTGGAGCGGAGCGACAAGAGCGGCAATCCTGAGGGCAGCGGCCGCCGCAAGAAGAAGAAAAAAACGCAAGAGTAAACGAGGTACAATAAGAGGCGCTGCTTCCTGTGTGAGGGAGCAGCGCCTTTTTGACAGAGTTATAAATGTTTGAGGGAAGCGAAGATTCCCCTTATCTAAACAATTGGGGAATTATGATTTCCCCTTCTTGTGGATAAGATGTGTATAAAGTTGGGGATAAATAGATATGAATTTGAGCGAATTCACCCAAAAGGTCGGGAATTATTCGGATCGATCGCCTTTTCCCAACTAGCGCTGGTGAAGTAGCAGGCGAGCAGGGTTAGTTGGAAAAAGGGAACTTATTTCTCCCCAGAATCAACAATTGTGAGGTTTAAGTGGAAAAAGGAAACTTAATTTAGCCATATTCCTTCGTAAGGAGCGAAATGAGCTGAATTAGTGATCCTTTTTCCAACTTAGGCTGCGGAGACCGGGGTGTTCAAGCCAATTAGTGATCCTTTTTCCACTTGGCATTGCGGAGGATTCATAAAGGGTTCTCCAGGCAACGCTATACTGAAATCCAAATCGGCTACCTTATCCAGCCAAGGATTGCGTGGCCATGTTTGTTCCTAAATTAGCATGAGACGTCTGTGCCGCCATACCAATCCCTCTATTATTGCAGAGATAGATGAGCTTCTGTTCGGTTCGGTGGTCATCCTTTCTTGCGTTAGCGTAAGCGCTTTTGGTACAATATAGATCTGACGTTTGACTCTGTTCAAACGGGACATTCGATGCAAGGGGTGACTTTCATGGGTAAAAAAGCAGACGGGAAAGTGCTCGCCCAGAACAAAAAGGCTTCCCATGATTATTTTATCGAGGACACTTATGAAGCGGGCTTGGTGCTGACCGGCACTGAAATCAAGTCGCTGCGTAACGGCCGCGCTAACATTGGCGACGCGTTTGCCACCATTCGGAACGGCGAAATTCATGTGCACAATATGCATATCAGCCCTTTTGAACAGGGGAACCGCAATAATCCTTCTGATCCGACGCGCACACGCAAGCTGCTGATGCATAAGGTGCAGATTCACAAGCTGCTCGGCCAGTCCAAGCAGGAAGGCTATTCGATAGTGCCGCTGAAGATCTATGTGCGCAATGGCTATGCGAAGCTGCTGATCGGCCTGGGTAAAGGGAAGAAGCAATATGACAAACGCGATACCGCCGCCAAAAAAGACGCTCAACGCGACATCCAGCGTGCGCTGCGCGAGAAGCAAAAGATCGCCAGATAAGCCGATTACCCGGCTCTTCCTGCCGTTCCAGATCTGCCCTTCAATTCCTTTAACCTACGTGTTAAAGTGTTGATAAATGTGCTATACTGTGTAAGTAAGATTTTTGCTTCGTGACAGTCCTCTGGGACAGAGGCTGTCTGGATCTCTCTTGCTGGAAGATCCGCTGATCCGAAGCGCCCTTTTCTAATGAGGGGCCGTTCTTGGATTCGACGGGGGTAGTTCGAGCATGAGCAGCGAGTAGTGGGGACGCGTCCGCTTCATCAACGCTAAAGCCTATTAAACGGCAAACAACAAAACAACTACGCTTTTGCAGCTTAATAACCTGTGAGCGTGCTTCTACCCTGCATCGCCCATGTGACAGGGATAGGGGCTAACAAGTAGTGGGATACGCTGTCTGGTCTCCGCCTGGGGTCAGCAGAAGAAGATAATCAGGCTGACCCAACGTATAGCCGGTTACGGGGCGATACTCGGGTGACATCAAAACTGTAACTACACTCGTAGAAGCTTATGTGCCGTTATCTTCGGACAGGGGTTCGACTCCCCTCGGCTCCATTGGTGAAAACCCTGTACGTGATTTCAGCTTCAAAGCGATTAATATCGCTAGAAGGTTGGATTACTACACGGTCAACGTATTCCTGAAGAACCTGCTTCTTTTCGTCTTCATTGCCGGAAAGGAGGAGGTTCTTTTTCATTTCAATGATGGACCGAATTTGGGTATCATCAAGAACGGCTACGCGCTGCATGACTTCAGCTCGATCCAACTCATACTCCAAAGCTTCCTTGCGCTGCTCGGCCTGTTTAATATTTTCTATGACCGTTTTTATGCCGGCACCAAGCGCTTCAATCCAATTCTTTAATTTGCCTTCAAGTTCAGCCAGTTCACGCTTAATAGGTTCGATGTCATTTACAGATTGTTGCTTCTCCTTCTGGTAGAGTTCCTGCACTTTGTCGATTATCTCTTGTATGCCTTCACCGGAAAAACATACTTCAATCAATCGCTGGATAACCATAGCTTCAATGTCATCTTTGCGCACACTCGTATTCCCGCACTTATCCTGGCATTTGTAGTAGGTCAGAACGGTGCCTTCGCTGCTTTTTTTGTTAGTATAAGAGTTTCCAGAATATAACGCCCCGCAAGCTCCGCAATAAATCTTACCTGTCAGTAGGTAATTCACTTTGGCTTTCATCCTCCCTGGCTTTCTTTTCCGATCCTGCAGTTTCCGGTATACTCGATCCCATTGCTCTGACGATATGATAGCTGGTATTCTGCCTTCATGCAGTACCTGTTCTTCTTGTGGCTTTTTATTATTGGTATTCCGTTTCCCATCTTCATCCTTCGGAGCTGAAACGTCATAAGTATAATCGCCCTTATATTTTCGGTTGTGCCCCCAGGTGGCAAAACTGCTGCTGGTGAAAGAACGGTCGTTTAGGGTTCTGTATCCTTTTTCATTTAATATTGCCGCAATCTGGTCATTGGATAAGTCTGCTTCAATACCATCAAAATATATTTGTACGGCCTTGTAAGTCTGCTCGTCTATCTCCAGCATACGGGTTACGGGATTGACTTTCAAGCCGTATGGGGGCCGTCCGCCGGTATGCGTCCCCTGCTCGGCATTCTCGCGCAAGCCCTTACGAACTTCTCGGGAAAGGTTGAGAGAGTAGTATTCGGCCATACCCTCTAGAACCGATTCCAGTATGACCGATTCCGGGGAATTGTCCAAGTGTTCCAGGACCGATTCAACCCGGACACCGTTCCGTTTCAGGACCCGTTTATAATGTGCAGAATCGTAGCGATTCCGTGCGAAGCGATCCAGTTTATGTACAATAACGACATCAAAAAGTTTTTTATTCGAATCTTCTATCATTCTCTGAAAGTTGGGACGTCTATCAGTTGTGGCAGTCTTCTCTTCGTCAGGGTAAGCGTTAACAAGTACATAACCCTTCTGCTGGCAATAAGCCTCTATAGCCCGCATTTGGGCCACAATGGACTCTTCACGTTGGTTGTCAGAACTGTATCGCGGGTAAGCAACGGCGCGAATTAATTTGTTGGTAGATGGCATAGATATCCTCCTTAAAGCGCCACTCACTTTTCGGTATTGTGATCCCTTTTCATCCTTAAAAACTCCTTAAACCGTTTTAATTCCTCAAGCTCTTTATCTGTCCAATCTTCTTCGTCAATGTTAGGTTTATTGATCTGTACAGTTTCTTCCTCATGTTTCAAATAATCTAGGTAAGCATTTATGTCACCTTTATAGTATTGGGTGATAGCGCCTTCGTACATTTCATATTTAATTAAAAATTCCTGGACTGTCATCCCCAAGTACCTGGTGATATTTCCTAGTAATTCAGAGGTTAAAGGAATCTTATTATTTTCTATTTGAGAAAGGGATTCCGGTGAAATCTGAATTGCAGTAGATAAGTCTTCCAAGGATACGTTTTGAGCTTCTCTTTCATCCTCAATATAACTGCCCAGATCATAGATATGTCCCCACCCTACAAGATCATCAATGGTTACTTTAAAATAACTGGCTACTTTTTGTAGTTTTTCTAGTGAGGGTGAACTTTTTATCCAATTGTAAATTGTACCGTTGCCAAAGCCGAGTTCTTTTTCTAGCTTTGGAATCGTCGTGCCGTTTTTATAACAGAGATTTTTTATGTTATCAACTATTTCCACTCCATACACTCCTAAAATAGATAATAATCCAATGTAAAACTGATTATAATCTAATTGTTTATTGACCTACCGATTATAATCGGTTATTATTACATCAACAGCTTAATTGATGGCAAAAAAGGCAACAAAAAACCAGAGGGATAGTATCCCACATTTAAAAATCGTTCCCCAACGACGTTTATTTGGTTATGCCTTCCTAACGATAATAGAATATTTTCGGTCAGGAGTCAACAATTTAGCTGATTTTTTACAAATTTTTACGAAGGAGGTCGAGAATATGACGCATTATAGCGAGTTTGGAGCTGAGGCAAGAAAGGTCATGCTTCAGAAGAAAATCAAAATGAAAGATGTTGCAAGCGAGCTTGGCGTTTCTGTTACCTACGTTTCTGAAATTTTCAAAGGAACTCGTCCGGGAGAGAGACAGAAGCCATTAATCGCAAAGATGCTCGGTATGGAAAGCGAGGTTGTTCATGAAAGCTGAAATTAAAACGACCATAAAGCTTATTCCTCATCCGGAGCCTCAGCGGTTAGTCGATATGTGGGCGCGGATCGTCGTGAACGAGATTCTGAAACAGGAAGCTGCCGAGAAAGGAGCTACCCCGTGACTATTAACCAGCAAGCCGAATCAGCTGATCACGTGTGGCGCCGGCTGGAGCTTCGCCGCAGACGCTGGCAACTACTTAATGGCCGACTGATTGTCGATGAGCCGGAAGCCGCGGTCTGGTGGTTGGATAAGGAAATCGCTGAAATGGAGGCAGGCCAGTGAAGACGCTACATTTTACCTATGATCCTTTAAGACTTGTACGGATCGTGCTGCAACGACATGTAGAAGAGACAATTCAAGGGAGGTTCTACAAAGCCAAGCAATTTGCTTGTTATGAATACCTTGCGAAGTTATCCGATGAAGGTTTGGAAAATCTGCTTCAGGAGTACACGAAACGCCATGAGCTTGAAGCTATCACCCTAGCAGATTGGCGGAAAGACGGGAAACTGATTTTTGACATCATATTTGAACAGCCGGAATACCAACAGCTTGAGATTGACTTCAAGAAGAGGGGATACGGAATAACCGGTCTCGGAGTGCTGGATGTGGAGAGCAACACTTTCTATGAATGTGGGTTTGCTCATCACTGGCAGGCAATTCAGAACATCATTGAAAAATCATATCCTAGATTCCATGAACCGTTACAGAGGATGTATTTCGATGAGACGCTGACGGAGCATGATGGGTTGACCCGTGAAGAACTGGAAAACTTCATCATGACGAACTTCGAGCTGTACGGCGGCACTAAGCCACTTCAAGAATACCTGTAAGACCATGAAAGGGGGTGAAAAAGCGAATGAATGAACCTGTAACGAAGCCGCTGGGCTGGGGAATGGTTGCGGTGATGATCGATAACCCGGTGGTGGGTGGCAAGCAGCTGCACCTGTTTGAAGCAGAAAGTACGATGTCTGGGGCATACGTACCGCCGAAGCAGATCAAGATTGATGAAGTCGAGAAGCTGAGGGACTTCCTGATTGAACAGATGCCGCCGGATGATTTGGTGAATCTGCTGTCCACTTTGGAGAAGGCGATACATGAAAAAGACGATCCATCGGCTGCAACCGTCTGAATCGTCCACAAGAAAAAATAATAGTTGAGGTCAGTGTACCACTGGCCAGAAGGAGAAATCAAGTATGGGATGCGATATTCATTTGTTTGTGGAGAAGCGGATCAATGGAGTTTGGCAAGTGGAGCGGGGTGTCAATGAGCCGGAAATCGAAGAAGTGCGGGGTTTCATTGATAAATCCAAGGAGCGCGGCGAATCATCTGCTTATTGGGAACGTCTCCTTGAAGAACTGCGTCAGGGAACAATGGATTATATCTATGATGGTCGCCATTATCTACTTTTTGAAGTCTTGGCCGGTGTACGTGCTGCGCATGACCTGAAGCCTGTTTCCAATCCTAAAGGGCTCCCGGAAGATATTTCACCAGAAGCTGGAGAATCGGCGGAAAGTTGGGGCGGTGACGGCCATAGCCATTCCTGGCTGACGGCTGCCGAACTGCTTGCCTACAACTGGGATCAGACCATCACCCGCGAGGGCTGGGTCGGAGTTGAGCAATTCAAGAAGTACCTGGAAGATGGCGAACCGTCAATGTGGAGCGGCGGCGTAGGCGGGGGCGGAACCAAATACATTTCCAACAAAGAAATGAAGGAAGGTATTCGTGACGGCTTCCTGTTCGGTGATCCGCGTCAATATTACACGCTGATCCACTGGAACAAGTCGCTCCGGGATGCTTTGGGTAAATGGTGCAGTTGGTCGCTTCCGAAGCTGGCCGAGCTGGCCGGGGACGATCCGGAGAGCGCTCGTATTGTATTCTGGTTCGACAATTAAGGGGGGGGGAGCACAATGGAAAATCAAGTGAAGAGAAAATCTATCGGTGAAGTTCTGGCTACAATCGATCCAGAAAAAGTGAACCTTCAGCTTGTGAAGCCGGCTTTAATGGAGGTTGCACGTTCTAATACTAAGCGCTCCGGATTTTTGAAAATCGCTGTAGATGATGATGTGGCAGTAGATTGCTTCCAAGCGATGCCGGATAAGATTCGCTTCATCATATCGATTGACCGTGAAGACTGGAATCGGGCGGTGGTGTCAGAATGAAAGCCTATGATTTTCAGAAAGCCAAACTCTTGATCGAACAGGACCGGGAACAGATTCAAGAGGCGGCACTTGGAATGTATGAGGATTGGTTCTGGACCGCTGAAGAAGTGTTCAACGACCAAGAAGGATTTGTTCGTGACTTAGAAACCGTCGAATTGATTGGTGGTATTAATGAATCTTCCTGGGCCACTCCATGTCTGCGTATTACCTATCGTGACGGAAACGAATCTTGCATTGGTTGCTTCAAGGATGATGGGTCACCTTCGGAAAGAGGCTTTGTGATGCCACTTGGAGTCCTGTCTGGACCTGCGCAGGATCGGATGCCGCCACTCACTTCAAAGGAGGGTCGTCATGATTAAAATCAATAAGCTCGAAATCGAGAACGTCAAACGGGTCAAAGCCGTGAAAATAGAGCCGACAGCAAGCGGGCTAACCTTAGTCGGCGGCAAGAACAACCAGGGTAAAACCAGCGTGCTGGATGCCATCGCCTGGGCGCTAGGCGGGAACAAGTACCGCCCTTCGCAGGCCGCAAGAGAGGATTCGGCCATCCCCCCATACCTCCACCTGACACTTTCAAACGGGCTGATCGTGGAGCGGAAGGGCAAGAACAGCGACCTGAAGGTGGTCGATCCGAACGGCCAGAAGGGTGGGCAGATGCTCCTGGATAGCTTCGTGGAAGAGTTGGCGATTAATCTTCCAAAGTTCATGGGCTCCACCAACAAGGAAAAGGCCAACATTCTCCTGCAGATCATTGGCGTGGGGCAGCAACTCCACGAGCTGGAGGTCAAAGAGCAGGAGGTATATAATCGCCGCCACGCCATCGGCCAGATTGCTGACCAGAAGGCCAAGTTTGCCAAGGAACAGACGTACTTCCCGGATGCGCCGAAGGAGCCTGTCTCCGCTTCGGATCTGATCCAGCAGCAGCAGGCAATTCTTGCCCGCAACGGGGAGAACCAACTAAAACGGCAGCGGCTGACACAGTTCCAGGCATTGTATGCCAACCAGGGACAGGAGGTTGAGCGGTTGAAGGCGATGCTGGCAGATGCAGAAGCAAAGTATGCTCAAACGGGTGTGGATCTGGCGGCAGCCCAGAAAGACGCTCTACAGCTTCACGATGAATCGACTGCAGAGCTGGAGACCAACATCCAGCAGATCGACGAAATCAATCGTAAAGTCCGCGCCAATCTGGATAAAGACAAGGCCGAAACGGATGCCAGCGATTACCGGCAGCAGTATGATGCGCTGACCACTGAGATCAATACGGTGCGCCAGCAGAAAACGGACCTCCTGACGAACGCTGATTTGCCGCTGCCGGGATTGACCGTAGAGAATGGGGAGCTTAAGTACAACGGCCAGTGCTGGGATAACATGAGCGGATCCGATCAGCTGAAAGTCGCCACGGCTATCGTACGGCGTCTGAAACCAGAATGCGGCTTTATCCTACTTGATAAGCTGGAGCAGATGGATATGGACACCTTGCAGGAGTTTGGTGCCTGGCTGGAGCAAGAGGGGCTGCAAGCCATTGCCACCAGGGTCAGCACCGGCGAAGAGTGCAGCATCATCATCGAGGACGGCTATGTTGCCGGGCAGGAAGGCGTAACCCTTCAGCAGTTGCCGGGCGAAATCGATCCGGGAGACGGGTGGAACGAAGCGGTTGCTCCCCCAACTTGGAAAGCAGGTGAATTTTAATGCAGGTCATTACTGGTAAGGTTCAGAAGGCCAAGAAGGTTGTTATTTATGGGCCGGAGGGGGTCGGCAAGTCTTCCTTGGCTGCTCAATTCCCACGCCCTATCTTTATTGATACTGAAGGCTCCACCACGGAAATGGATGTGGCACGGCTGCCGAAACCTTCGAGCTGGGAAATGCTCAAACAGCAGGTCAAATGGGTATGGCAAGGCGGACAATATGGGACCCTCATCATCGATACCATTGATTGGGCGGAAATGCTCTGTGTAGAAAGCGTATGTTCGACGCACCAAAAGAACGGCATTGAAGACTTCGGATATGGGAAAGGGTATATTTTCGTCTCCGAGGAGCTGGGCCGTATGCTCAACCTGCTCAGTGATGTCGTGGATGCCGGTATCCATGTTGTGCTGATTGCTCACGCTCAGATTGTGAAATTTGAGCAGCCGGACGAAATGGGCGCCTATGATCGTTATCAGCTCAAGCTTGGCCAAAAGACAGCAAGCCGGACGGCGCCACTGGTCAAGGAATGGGCCGATATGGTTCTATTCATCAATTATAAGACGTTCTCCATTGCCACGGACAAGGAAGGCAAGAAGAACAAGGCCCAGGGCGGCGTGCGCACCGTCTACGCCACGCACCACCCCGCGTGGGATGCGAAAAACCGCCATGGGCTGCCGGATGAGTTTCCACTGGATTATGGCCATATCGCTCATATCTTCAATACTCCGGCACCAACGACTAACCCATCACAACAACAGCAGGCATCAGTAACACCGCCGCAACAGTCAGCGCAAACAGTAAATCAAACAGGAAATATTCCAAATAATATTCCAGCTCCCGTAAACACTGCACCACCGACACCTAGCCTGAACTCAAATATCCCGCCGGCGCTGCGGGAACTGATGACCCTGCACCAGGTGACGGAATCGGAGATACAGCAGGCTGTTTTTCAACGCAACTATTACCCGGTAGATACGCCAATCGCCAACTATGACCCCGGGTTTGTGGAGGGTGTGCTGGTGGCAGCCTGGTCGTCAGTTTTAGGGATGATTCAAAACAATCGGAAAGCTGTTCCATTTAATTAAAAACTTCTAGGAGGACTTATACATGAGTGAACAAGAACGCGAATTAGGTTGGGACGACACTATTGAAAAAGACGGCGGGGAGTTTACCCTGCTGCCGGCCGGGGATTACCCGTTCACCGTTACGAAATTTGAGCGCGGGCGCTTCAATGGCTCCGATAAGATGCCTGCCTGCAACCAGGCGAAGATTGAGCTGACCGTGCATTCGCAAGAGCATGGGGATGTGGTTATCTTCCATAATTTATTTTTGCACACCAAGACCGAGGGCTTGCTTTCTAACTTTTTCGCAGGGATCGGCCAGAAAAGGAAGGGCGAAAAGTTGAAAATGAACTGGCAGACGGTTATAGGCTCCAAAGGTCGGCTTAAGCTGGAGGTCAACAAGTTCAGGGGGCGGGACGGAGAAGAGCGGACCAACAACCAGGTCAAGAGTTTCTACCCGGCAGACGAACAGCCTGCAGGACAGCCTCCGCAGCAATATCAGCCACAACAGCAATATCAGCAACCGCAGCAGTACCAACAACCACAGTACCAGCAGCCTCAAGGCGGAGCAGCGTACAATCAGCCGCAGTATCAGCAGGCCCCGTTCCCGGACTCTCCGCCGCCTCAGCGAGGCGGTAACTGGTCTAACGGACAGTTTTAGGTGGCTGCCATGGAACTTAGACCATATCAACAAGACTCCCGCGAATCAATTCAAGCGGAGTGGGAGAAGGGCGTCCGACGGACGCTCCTGGTCCTCCCCACCGGCTGCGGGAAGACGATTGTATTTTCCAAAGTGATTGAAGATCGGGTAAAGCTGGGCGAGCGTGTGCTTGTCCTGGCTCACCGGGGGGAACTGCTGGACCAAGCAGCCGATAAGCTGGCAAAGTCTACCGGGCTGGGATGCGCGACCGAAAAGGCCGAGCAAACTTCCATTGGAAGCTGGTACCGTGTCGTGGTCGGCAGCGTGCAGACCATGATGCGTGATAAACGGCTGCAGCAGTTTGCCGCTGACCATTTTGACACCATCATCATAGATGAGGCTCACCATTGCTTATCAGACAGCTATCAGCGGGTACTGGACTATTTCAAAGAGGCCAATGTGCTGGGCGTCACGGCCACGCCGGACCGTGGGGACATGAGAAACCTAGGTTCCTACTTTGAAAGCCTAGCTTATGAGTACACACTGCCCAAAGCCATCAAAGAGGGTTTTCTAAGTCCGATCAAGGCCATGACGATTCCGCTGAAGCTGGACTTGTCCACAGTCGGTCAACAGGCTGGGGATTTTAAAAGCAGCGACTTGGGTACGGCGCTAGACCCATACTTGGATTCCATCGCCGGCGAAATGTGGAGGGTGGCCAAGGACAGAAAGATTGTCGTATTCTTGCCGCTGGTGAAGACCAGCCAAAAATTCACTTCTATATTAAATGCGGTCGGCTTCCGGGCCGCCGAAGTCAACGGTGACTCGCAGGACCGGGCAGAGATACTGGCCGATTACGATGCAGGTAAGTATAACGTTCTGTGTAATTCCATGCTGCTGACAGAGGGCTGGGATTGCCCCAGCGTGGATTGCATCGTGGTATTGCGGCCGACGAAGGTTCGCAGCTTGTACAGTCAGATGGTTGGGCGCGGTACCCGGCTATTCCCAGGCAAGGAGGAGCTGCTGCTGCTGGATTTTCTGTGGCACACGGAGCGGCATGAGCTTTGTCACCCGGCCCATTTGATTGCAGAGAATGAGGAAGTTGCCCAGGCCATGACTCAGCAGATCGAGCAGGCGGGCATTGCGTTAGATCTGGAAAAGGTTGAGAAGCAGGCCTCTGAAGATGTCGTTGCGCAGCGCGAGGAAGCTTTGGCCAAACAGCTGGCCGAAATGAAGCGCCGCAAGGCAAAGCTGGTTGATCCGCTGCAGTTTGAAATGAGTATCCAAGCAGAGGATTTATCTGGATATGTACCCTCATTCGGCTGGGAAATGTCGCCGCCGTCCGAAGCGCAGGTAAAGACCCTGGAGAAGCTGGGCATCCTGCCTGAAGCCATCGATAATGCCGGCAAAGCAACGAAGCTGCTGGAGCGCTTGGATAAACGCCGTTCCGAGGGGTTGACCACACCGAAGCAGATTCGCTTCCTGGAGAATCGTGGCTTTGAGCATGTCGGTACCTGGTCGTTTGATCACGCCAAGCGCCTGATTGACCGCATTGCCGGAAACGGGTGGCGGGTTCCGGAAGGCATCAATCCTAAAGAATATCGCGGGGAATAGAAAAAACCTGGAGGAAATATTCCCTCCAGCCAAAAATAAAATGCTGTTAATTTAATACTTCCCACCCATGGGCTTTATAGATTTCCTTTCTTTCCTCAATAATGTTTCTATCTTCAGAATCAATAGATACGGTTTCGAGATAAGCAAGATAATAATTTTCTTCATAATTAAAGGATGCTTCTGTAACTGTATAAGCAGGGTCATTTCTATGATAGACACTATCTTCTATTGCATCTCCAATTCTAGGCAGAAAATCGACATCGGCATAGAGTTTACGAGCTGTCAAAGAATCACGAAACTTATGTTTATCTTTCAGATGAACATATTGTTGAATTATTAGATTCATTTTTATGTACCCTCCTTCGTTATATAAAGCTAGTATAGTATCACTTATTTTTAACATCAAGAAATATTTGACAAAATGAGCCAATGAGAGGTAAAGCATATGTTCGAAAAAAAATTAAACCTCACAACCTTGTTGGAACATGTTGATCCGTCATACCTGAATTACCAGGAGTGGGTCAATGTTGGCATGGCCCTCAAGTATGAAGGATACACAGCCAGCGACTGGGACGAGTGGAGCCGGCGGGACGGCGGGCGGTACCATCCGGGCGAATGCTTTAAAAAGTGGACCAGCTTCGAGGGTAACGGCAATCCGGTGACCGGGGCGACCATCACGCAGATGGCCAAGGATAACGGCTGGCTGCCGCGCTCCGCTTATGACCGGGAACTGGATTGGGACGATGAGATTTCCGGCAGCTCCGGTGATTATGTCGTCGTGGATAAGAATTGGATTGAAGGGAAAGAGATTCATGAACCCGCCGAATGGAACCCAGTGCAGCAGATAACAACGTATATAGGCGCTTTATTTGAAGCTTCTGAAAATGTGGGCTATGTGACAGAAGCCTGGCAAAGTGAAGAAGGGAAATGGCTACCCAACAAAGGCGCATACGACCGGACGGCGGGGGAGCTGATTGAGCTGCTGCATATGTGTGACGGCGATATCGGGCAAGTATTCGGGGATTACAAGCCGGAAGCGGGGGCCTGGATACGATTCAATCCGCTGGATGGCAAAGGCGTGAAGAACGAGAACGTGACGGAGTTCCGGTATGCCCTTGTCGAGTCCGACACTATGGACATTGAAAAGCAGAACGCTGTCATGCGGGAGCTGGAACTGCCGATTGCCGTTATGGTCTACAGCGGCGGGAAGAGCCTGCACGCCATTGTCAGGGTAGAGGCTGCCAATTACGACGAGTACCGCAAGCGGGTGGATTACCTCTATGATATCTGCCGGCGGAACGGTCTGGCCATCGACAAGCAAAACCGTAACCCGTCCCGGCTGTCCCGGATGCCGGGAGTGGAGCGGAACGGAAAGAAGCAATTCATCGTGGACACCAATCTGGGCAAGGCGAGCTGGGCGGAATGGCATGAATGGATTGAAGGCATCAATGATGATCTGCCCGATCCGGAGAGCCTGACAGAATCATGGGACAACATGCCGCCGTTGGCTCCTCCTTTAATAGAAGGGATGCTTCGGCAAGGTCATAAAATGCTCATGGCTGGACCGTCGAAGGCTGGGAAGAGCTTCGCACTGATTGAGCTGAGCATCGCTATAGCCGAGGGCATTAAGTGGCTGGCCTGGCAATGCACGAAGGGCAAGGTCCTATATGTCAATCTGGAGCTGGACCGGGCCAGTGCCCTGCACCGCTTCAAGGACGTATACAGAGCGCTGGGGATGCCGCCTCATAACATCGGGAACATAGACATTTGGAACCTGCGTGGTAAGTCGGTACCGATGGATAAGCTGGCGCCGAAGCTGATCCGGCGGGCGGCCAAGAAGAACTATATTGCGGTCATCATCGATCCCATTTATAAGGTGTTGACTGGGGATGAAAACAGCGCCGACCAGATGGCCCACTTTACGAACCAGTTTGACAAGATTGCCACGGAGCTGGGGGCCAGTGTCATTTACTGCCATCATCACAGCAAAGGCTCTCAGGGTGGCAAAAAGTCGATGGACCGGGCTTCCGGCAGCGGCGTATTCGCCCGCGATCCAGACGCTCTGATTGACCTGGTGGAGCTGGAGGTCACCGAGGCGCTGTACATGCAGGAAGAGAACAAGGCGATCTGCAGCATGTACAAAGGGCTGTTCCAGCAGTATAACCCGGCGTACCTGCAGGAACAGGTATCGCAGGATGATGAGCTCAGCGCGAAGGCTATGGAGGATCACGCCAAACGAGCGATGCCACATGTCATGGAGACTATCAAGCCGACCATAGAGCAAGCGCTTGAGGCCGTCCGGGCGCGTTCGGCGTGGCGTGTGGAAGGAACGCTGCGGGAATACGCCAAGTTCAAGCCGGTCAATATGTGGTTCCAGTATCCGGTGCATCGCGTTGATGACACGGGCAGCCTGAAGGATATCGAGCCGGAAGGTGAGTCCAAACCGCCATGGCAGAAGGCTACCGGGAAGCGGAAGAACAAGGCCAAGGAGGAGCGCCGGAGCAAAGCGGATGAGTTCGCGGACGTGGTAAGCAATTGTAATTTCGGTGAGCCGCCTACTGTTTTAGATGTCATAGCATGGTATGGATCAACCGGAAAAGAGGTTGCCGAACGCACCGTTAGAGATTGGATTAAACGGTATGGCTATGAAATTGATCGTTCATTGGGTTTCCGAATTGTTAAAAAAGAAGAAGAGTAATTGCGGCGGCGATCATCGTTTCATGGTCATTGCAAAATGTTGCGGCGACCATAAATTAATGATTGCCGCAAATTGCGAAACATGGTCGCCGCAATTCCGCAATAAGTTGCGGGGATTCTGATACGTCATGATTGCCGCAATATGTGGTGGCGACCACTATATATAAATATATAAGGATAAGGGAAGGGGGTATAAAAATCCCCCTTCCCCCTCCCCTACATTTATCACCGCGAAAAAAAAGTTAAAAGTAAAAAAATGGAAGGTGACGATATGCCGACTGAGTTCTTCATGCCGATGAAACCACCGACCGCTACACATCAAGAGAAGCAGGTTGCTGTCGTCGATGGTAAGCCAGTATTCTACGAGCCGGACGACTTGAAGGCCGCGAGGGCGAAGCTGACGGCTCACCTTGGAAAACATGTTCCGCAGAAGAAATATTCCGGTGTGGCACTCCGGGTAACAGTGAAGTGGCTGTTTCCGATTCCAGAAGGCAGCAAGCACTATGACGGGGAGTGGAAGAAGACCAAACCTGACACTCACAACCTGAATAAGCTGCCATTCGACATTATGACAAATTTAGGGTTCTGGAAAGATGACGCGCTTGTGGCAAGCGAAATCATAGAAAAGTTCTGGGCGAAGCTGCCGGGCATTTATATCAAAATCGAGGAGCTGTAGGCCGTGGACTATAAGGCACTGTTCTGGGATGTGTACCTGTGGACGCAGCAGGTCAACGAGGCAGCCGCCCGGCATGGGATGCAGAGCCCGGACTTTTGGCAATGGGTCGCTGACTCCACCGGCGCGATCTGCTGCAAATATAACGACCACCGGCTGGCCATCAAGCAAATGCTGATGATGATCGAATGGCTGGAAGAGGTGTATGAACAGCAGAGGGGACGAGGGTAATGATTTTGGTTTGCCTGGAGTGCGCTGCTGATATGACGGAGATCAAACCAAATGTATACCGCTGCCCGTGCTGTGGCTGGATAGCTGAGCAATTAACAATAAACAGAGAGGATGATCTGGATGAGTCCTGACCCTTTCTTTCAGGATATTCCGTGGGAGTTCATCACAGATGATAGTGGCAAGGTGATCGGAGAGGTCTTCCTGACTCTCCCGGATCCGCCACTCAGAAAGCGGCAGCTCAAGTGGGGTACCACAACCGCTAAGGGGGTGCACCAGTTATGTCAATGATTGACCGAACCAACGGGTCACGGGTGGGTTACTCCGGCACATCAATACCCAACCAAGCGATTGAATACAAGTCATACGGTTCCGGCACCGTCCGGGAATATACGCTGACGCCGGAGGAGCTGGAAGAGGTCCGGCAGAAGTATCCGGCCACGAAACGGGATAAAGCATTCAAAAAGCCGGTAGCACACAATCCAAGAGAAGATCGGTTTCCCCCGAAACAACAAAGCCAAAATACTGAGGAGGAACAGAATATGACAGGTCAACGAATGAGCAAAGAGGGACCCAGCAGCGGGCTGACCAAGCAGATATTTCTGGAGCAGATTGCTTCAGGGGAGACGGTGGCCAGCGTGGAAAAGGCGTGGGGGATGAAATACAATACGCTGTCTTTCTGGGTGAAGAAGTGGGATTTGAGAGGCATTAACGCAGTCAAAGCGCAGGAGCTGCTTGCAGGTGAGTCGCCCAGGGAAACCCAATTGCTCCGCGAAAAAGAGGCACTGCCGCCGGTGGGGCATCAGGCGGGAGAGGTCGAGCGCCTGAAGGCAGAGGTCGAACACTGGAAGGTCCAAGCAGCGGGCTGGAAGAAGGAAAAGGATGCAGCTTGTGAGTGGGGAGAAGAGCAGAGGAAAAAGGCTGTTGAAGCGGTAGCCCTTGCCGGCAAGGCTGCCGAGGAGTCTATGGCCAAGATCGAGCGGCTTACAGCAGCGCGCGACGGGGCCATTGCAGCGCGGGAAGCAGCCGAGCTCGATCTGGAGCAGACCGAGACCCGCTGCAGCCAGTATGCTCAATCCATCGACCAGCTTGCAACGGAGTGCGACGGGCTTCAGGAGGAAGTCAATCGCTTGATCACCGAGCGGGATGATCTGGTGGCCGAAGTGGAAGACCTGCGTGACGATATCCGTCGGTTACGAGAAATTCAAACTCTAGCAGCTGCGCCGGCCAGCGATGTGCACCTGCTGGACCGGAGCATCGCGGATCTGACGCGGGCCAAGTGGATTTTGAACCGGCTGACAGCTTCCGGCGAATAATACGACAGGGGGTCAGGCAACATGACAGAGCAGCAAGTGATTGACCAGCTCTCCAGCTACCGGGCAAAGCTGGCGAGGATCCAGGCCCTGGGGACATACAGCATAGGCAGCGGGATTCAGATCAGCCGGCTTTCCGAGGAGGACCATCTGCAGCAGCTTCACCGGCGGCTGCGGGGCTTGCCCAGTTACATGTACCTTGGCAAGCGTGATCAGGAGTTGGAGGCTACAGCGCACGCCTACCTGACGTTCTACCCGGCAGGCGTCCGGGCACAGCGAAACGCGATTTCCGACATTGGAGCTTACCAGGAGGACGATGAGCTGCTGCAGGAGCTGAGGGCCAAGATTGCTAAGGTGATCGATGCACGCGCCGGCAGCAAGTACGATCTGGACGAGGTACTGGACCGACTGAGTGAGCTGCAGGATCTGCAGGCAGAGATCAAGCGGATTGATGATCTGCTTTCGCTTCTGGAAGGGTATAAGCCGGATTACTCCAGAATCCTTTACCAGGACGTAATCAGCGGACGAAACTGGTCAGAAGTCGCGAAAGAAATGGCGTTATCCAAGAGCGTTTACTTCCGGTGGAAGAAGCATGCAATATCAGCCTTTATCAAACTGGCAGAATAAGGTGGGAATGAAACGGGAACGGAAAGGGAACACAAGCCATAATTTCCGTGTTATTATGATATTGTGAGAGAATTATAAGTACGAGTTAGAGCCGCTCGAAAGCGGCTCTTAAAATTGTTTAAAATCTAAACGAAACCATTGTCTTTTAATCTCCAGGCAATGGTTTCGTTTTTATACAACACAACGCGTATCATTTCTATTTTCTCGGGGTGTTAAACCTTCTAAAGAAGTTTCAAGTCATTAATTGCTATGAAACCTTGGTCACTTGTAATTTCTAACTTTAGAGTTAAAAAAGCACCTGGTTTTGATAATCTAATTACAGGCATTGTTAATATTTGGGAATTTTTAACATAGTACGTTACAGGTTCAGAGACTTGATCATAAGCTCCTCCATATTTCATCCCCCAAACAACAAAAGAATAAAATACTCCCGGTGCCCCTCCTTCGTAATGGGTGGTGATGTATAATCCCGAAACATTGGTTGCATCCGGGAATTGTATGTCTAGACTATCTGCAAATGAAGGATTATACCAGTAAGTGTTAATATTGGTATCCTTAACATTTTCAGGGATATAGTTTTCACTGTAAGGTGCTTGTACAGAAGTATTCACCGGAAGGGGGAAAACTTCATAAGAGCTAGCTGAAGTCAAACCAAATATCCTGGAGGAATTGTGGTTTGAAAAGTTGGATCTGAAAGCTGAATTGTTTGTTTGTTGATTTTGTGTAAGCATTTTTATGGGCCTCCTAATTAATTTATGACTTTATGTTGGCTTCCCCGATAGCATAATATGCATACAAATTTAAAAATCATAGTATTAAAGGAGGCCGCCTACATGGCGCTGACACCGAAACAAAAGCTTTTCGTGCAAGAATACCTGATCGACCTCAACGCCACGCAGGCGGCCATTCGAGCGGGATACAGCCCCAAGACGGCGGAACAGCAGGCAAGCAGGCTGTTAAGTAATGTTAAGGTGCAGGAAGCGATCAGAGAGGCGCAAAGCCATCGTGCAGCTCGCACCGAGATTACGGCTGACATGGTACTGCAGCGTTGGTGGGATATTGCTACTGCAGATCCTAATGAGCTGATCCATTTGCGCCGTCTGGCCTGCCGGTACTGTCACGGTAAGGATCATCAGTACCAATGGCTGGACGAAGAGGAGTATACTCAGGCCGTCAAGGATGCTATTGATTCCGCTGAATCCGAGTCAAAGAAGCAGGATAGGCCTGTCGAAGCGATTCTGCCATCTGAAGACGGGGGGTATGGTTTTGACCGCCTGGCTGATCCACACCCTAAATGTCCGAAGTGCCGAGGCGAGGGCCGCGCTGATCTGCATATCGAGGATACCCGCAAGCTGAAAGGCGGGGCGCGTCTCCTGTATGCTGGGATTAAGGAGAACAAGAACGGTATTGAGGTTATCATGCAGGACCAGGCCAAGGCCCTTGAAAACGTGGCGCGGCATCTTGGCATGTTTGTTGATAAGGTGCAGCACAGTGGCAATGTGGATCTTAACATGAATAACCCATACAAGGACTTGACCACTGAAGAACTACGGAAGCTGGCCCGTGATGGTTGATCTGACCGTAATCCGCCGTGGTGCCCGTGTGGAATTGGCCCGCCGTGAGTTTTTCAGCTTCTGCCAGGCCATGGCTCCAGATTTCTACCGGGATGATCGGCAGTATCTGATAGACCTGTGCGGGGAGCTGCAGGAGTTCTACGAATCCACAGACGATATACTGGTGGTCAATCTACCGCCCCGGCATGGGAAGAGCCGCACCGCTTCGATGTTTGCACAGTGGGTCTTTGGTAAGAATCTGATGGAGAAGGTCATGACAGGATCTTACAACGAAACATTGTCCACCACGTTCAGTAAGGCTGTGCGGGATGGCATAGGTACTATCAAGGCTGATGAGAATCGGATCGTATACAGCGATATCTTCCCCCAGGTGAGGATCAAGCGCGGGGACGGGGCCATGAACCTGTGGAGCCTGGAGGGTGGTTATAACAGCTATCTGGCCACGTCTCCCACGGGTACGGCAACCGGCTTCGGGGCAACTATCCTCATGATCGACGATCTGATCAAAAACGCCGAGGAAGCCAACAACGAAAACGTACTGGAGAAGCATTGGGAATGGTTCGTTAATACGATGCTGTCCCGGCTCGAAGAAGGCGGCAAGATAATCATCATCATGACCCGCTGGGCCACGGGAGACCTTGCAGGGCGGGCGCTGGAGCATTTTGCTGAGGAACATAAGCGGATACGACTCTTGACCATGAAGGCTTTACAGGATGATGGTACGATGCTCTGTTCAGACATCCTGTCCCGCGCTTCTTACGAAATGAAGTCCCGGGCCATGGGGGAGGATATCGCCAGCGCAAACTATCAGCAGATCCCGATAGATATCAAGGGTAAACTGTACAGCAGCTTTAAGACGTACACGCAGCTGCCCACGGATGGCCACGACGAGCCGCTGTTTACGGGGATCTATGCTTATTGCGATTCCGCTGACGAGGGTGATGATTACCTATGCAACATCATCTGGGGTGTGTACCAGAAAGAGGCGTATGTCTTAGACGTCATATATACTAAGCAACCTATGGAGATTACAGAGCCAGCCACAGCGCAGGCTCTTTTTGCGTTCAAGGTCAACAAGGCCCGCATTGAGTCCAATAACGGCGGTAAGGCCTTTGCGCGGAACATCAAGCGTATTCTGGAAACGGAGCTGAAGAGTAACCGGACCGATGTGAGCTGGTTCCACCAGTCGAAGAATAAGACGGCCAGAATCGTCAGTAACGCGACATGGGTTATGCAGCATATCTACTTCCCTGTGAACTGGCGGGATCGCTGGCCGGACTACTACAAGGCCATGACGAGCTATCAGCGGGAAGGCAAGAATGCTCATGATGACGCGCCGGATGCCACAACCGGTGTAGCCGAAACGATGTTCCTGTTAGGGGGTTAAGAGAGTGGGGTGGTTTAAGAACATGGTCATGAAAATGCTAAGGATCAACCCGGCGCCGGAAAGTCAGATTATCACGATCCAGGAGCCGTACAGCTATAAAGCCAACGTGCTGCGTAATCGGCTGTGGTATCGTGGCGATCCGTCCGAGCTGGATCAATTCTATAAGCAATCGGTGACAGACAGTGTAGGAAAATCCCGCTTCTGGGCGGCGGTGCCTACGGCTGGCCTTGGCATCCGGAAGATTCACAGCGGGCTCCCGGCCATGGTGGCGGATCGGCTCTCTGATATTGTGGTTGCCGATATGGACGCGATAACCCTGAAGGTGCAAGCTGAGACGGCCACATGGGAAAAGATCAGCGAGGACAACGACTTTCCAGAGCTGCTGGCCGGGGCTGTTACAGAGGCGCTGTTCGTGGGGGATGGGGCGTTCAAGATCACGGTGGACCCGGAACTAAGTGAGTATCCGCTGATAGAGTTTTACAGCGGTGATCAAGTAGAGTACAAGCGCACCCGTGGCAGGCTGCAGGAGGTCATTTTCTGGACGGACTATACCGTGAGCAGTAAGGATTACCGGTTGGAGGAGACATTTGGGCTGGGGTACATCCGCAGCCGGTTACTTGACGCCTACGGCAAAGAGGTGCCACTATCCGTTGTGCCAGAGACGGCCCAGCTCAAGCCGGAAATCACTTATGACGGTGACTTTATCATGGCTGTGCCGCTCATGGTGTTTAAGTCTACCAAGTGGCCAGGTCGAGGGAAGTCACTGTTTGACACCAAATCAGACAATTTTGACGCGCTTGATGAGGTGGTCAGCCAGTGGATGGATGCAATACGCTCCGGGCGGGTACAGAAATACATTCCCGAGGACATGATTCCGAAAAATCCAGAAACCGGGGAGCTGATGCGACCTAACCCGTTTGATAATCAGTTTATTCGGATTAATAGCACCTTTGCAGAGGAGGCCAAAGGGCAGATCAACCTTGTGCAGCCTCAGATCCTCTATGAGGCGTTCGTGGCTTCCTACGCTTCAGCCGTTGACATGTGTCTGCAGGGCATTATATCGCCCAGCACTTTAGGCATCGACTTGAAAAAGACCGATAACGCGGAGGCCCAGCGGGAGAAGGAAAAGGCCACGTTATACACCCGGGGCAAGATCGTGGAACGGCTGAATGAGGTCATTCCTCAGCTGGTGCAGACGGTGCTAAAGGTGTATGACACGATGCAGAGCCGCGCAGCAGGCAAGTATGAGGCCAGCGTGACCTTCGGGGAGTATGCCAGCCCGAGCTTTGACGCCGTTGTCGAGACGGTCGGCAAGGCGCGGACATTTGGCGTCATGTCCATAGAACGTGCCGTAGAGGAAATGTACGGCGACACCTGGACCGCTGAGGAAAAGGCCGAGGAGGTCGCCAGGCTGAAGGCGGAGCAGGCCCCACCTACCTTTGACGAACCAGGAGCTAACCGTGACGCTCCTCCAGGTGAGAATGAGGATGATACGGGCGGCGAAGATGAATGAGGAAATATGACATTCGCGGTATCTACGCTCAGATGGAGATTGACCTGATAGCCAGCATGAAGCGGAATCTGACCCGTCATGAGAATGAGGAAAAGAAATTAGGCTTTAAATGGCCACAATGGCAGCAGAAGAAGCTTGAGGATTTGCAGCAATACAAGAAAGAGGCCGCTCAGATCGTCAAGAAGGCAGAGCCTGTTATCGAACAGGCCGTCGAGCAGGAGATCAAAGGGGGCTTCTTTGCGGGGATTAAGCGGACAGCCATGAAACTCCTGGGGAAATTCATGCCGCTGCCGCGCAAATTGAATATCCCTGATGTTTCTGACGAGAACTTTTTCAAGCTGAACGAAGGCCGCGTCAATGCACTGGTAGAAGCGACTCAGGGTGAGCTTAAGGCTGCCCGCTTTGCCATTCTGCGGCAATCTGACGATGTATTTCGGCAAACTATATTCAAGTCCCAGGTCTATCTAAATTCTGGTGCTGCTTCTCTTGGCCAGGCTATTGATATGGCCACACGGGACTTTCTGGATAAAGGATTAGATTACATCACCTATTCAAATGGGCGCCGAGTGAATGTCGCTTCCTATGCCGAGATGGCGTTACGTGCCTCTTCCCAGCGCGCTGTCTTTGCAGGGGAGGGAGCTAAGCGGCAGCAGATGGGCAATCCGTTCGTCGTGGTATCGGCTCATAACAACTGCTCAGAGCTGTGCCTGCCCTGGCAGGGTAAAGTATACATTGATGATGTATACAGCGGTGGCAAGGCTTCTGATGGTCCGTATCCGCTACTCAGCAAGGCAATGGCCGCCGGATTGTTTCACCCTCACTGTCGCCATAACATGACCACATTTGTGCCAGGCGTCAGCCGGATGCCGGAGCCAGTAGACAATACCGAAGCTTTGGCAAACTACAAGGCCGAACAGCGCCAGCGGTACATGGAGCGGCAGATCCGCAGATACAAGCGCCGCGAGGCTGGCAGTGTGGACCCAGACAACCAAGCTGCAGCAGCCGTTAAGGTCAAGGAGTGGCAGGGCAAGCTGAGAAATCATCTTAAGACAAACGAGCATCTGCGCCGTGATCCAAACCGAGAGAAAATCCTGGGCGGTGTTTCTCAGGCTGAACATAATGAACTCTTGAAATTGGCGGCTAAAAATGCCAAGATTAAGGAAACCCGAGCGCACATTCGTTCGGAAGCTCAGCCAAAGAAAATTCTAACAGGGCAGCAGAACAAGCATATACCAGGGACACATGAGTATAAGCAATATCAGGCGAAGTACGAGAAGAAGGGAGAAACTGGCCCATCGTATCTTACGATTCCACCTGATCAGATTGAGCCCTTGGTTAAGCAATACGCGGGTACGGGCGAAATTAGGCTGAACAACAAAGGTGAATGGAACCATAAAGAAACAATTATGACCAATGATGCGGTGATCGGTAAAGCTGTGAACAATCTGACAGGCGCGGAAGCTGATACTACTGTGTTCATGATTCATTATGCTAAAGATGGAGTTCATGTCGTACCGGCTTACCCAAGTCTAAAGAAAGGGAAGGGAAATGATGGATTATCATGATCTGATCGGTGAGCGGGTCAAAGTGGTGGATAAAGACGGCGATGTCTATATTGGTCCGCTCATCACCTATGAGGTTGGCTTGGACAGTGACGAAGATTTTGATTCAATCGGCATTAAAACAGGGGAAGGCTATTACGAATCAGTACCTATTCCTGACATTGTAAGTTGCGAAGTTTTAGAAGATTGAAGCACTCACGCATATAGCGAGGGTGCTTTTTTGATGGGCTCCGGTTGAGACTGCCGGGGCCTATTTGCTCATGGGCCGGAGCATAGCGGCCCGCTCCCGTAGCTGGAGAGCAGCTATAAAAATCTATGGAGGTTGATGAACAATGGAATGGCTGAAGGAACTGCTGAAAAAAGCAGGCGTTGAAGAATCGAAGGTAGACGGCCTAATTGGTGACGTGAATAAAGAGCTGCCGAAGCATTTTGTTCCGAAGTCACAATACAACGAGCTGACTGATACCAAGAAGAAGCTGGAGAAGGACATCACAGACCGGGATACACAGCTTGAAGCACTCAGCAAGGATGCAGGTGCTTCCGAGACGCTGAAAGCCGAGATTGCCCGTCTACAAGGCGAGAACAAGACCACCAAGGAGAAATATGAAGCGGATCTGAAGGACATGACTTTGAACAATGCCATCACGGCCGCACTAAACGGCAAGGTTCATAACGAGAAGGTCGTCACTGGGCTGATCGACAAGAACAAACTGGTGATTGGTGACGACGGCAAGGTGGTGGGCCTGGATGAGCAGTTAACCACGCTTAAGACTTCTGACGCTTACCTGTTCAAGCCTGATGAGCCTGGTGCTGGTGGAGGTCCTGGCGGCTTTCGTGTTGGCGGCGGCGGTAATGGTAGTGGAGCTGGACAAGCAACCAATGAACAGCTGGCCAGCATTTTCGGTGTCGCAGATAGCAAGCAATTTTAATTAACGAGGAGAGATGTATAAATGCCTTACAACTACGTAGACAGCTTTTTGACGGTGCTGCAGCAGAAATACACGAAGGAATTGACATCAAGTGGATTGACCACTCAGAACGCGATCTTTGTCAACGCCAAAACGATCAAGATTCCGCGCTTGGATGTGGCGGGATATAAGAACCACAGCCGGGCAGGCGGGTGGAACCGGCAAGCCGTATCAAATGATTTTGAGCTGAAGGTGCTGACCTTTGACCGTGACGTGGAATTTTACGTTGACGCGATGGACGTGGATGAGACGAACCAAATCGTATCTGCAGCAAACCTGACAAATGTCTTTGAGACCGAGCAGGCCATCCCTGAACTGGACAAATACCGATACAGCAAGATTTATGCGGATTATGTGGCCCTGGGCAAGACTCCGGACACTACAGTCATTACAGCAGCTAATGCGCTTCAGGTCTTCGACCAGCTCATGGAGAATATGGACGAGGCAGAAATCCCGTTGGAAGGCCGTATCCTTTATGTGACCCCTGCCATTTACAAGCTGCTGAAGCAGGCAGAGGATGTACAGCGGTTTATCAGTGTGCAGTCCAACAACGGTACTGTTGATCGTTCTGTTCGCAAGCTGGACGATGTGACGCTGGTCCAGGTTCCATCCAGCCGCATGAAGACAATCTACGATTTCACTAACGGCGCGGTTCCGGGCGTAGGGGCCAAACAAATCAATATGATCCTGATTCACCCTAGCTGTGTCCTTGCTCCAATCAAACACACTGCCATTTACCTGTGGGAGCCTGGAAGTCATACAGGCGGAGACGGTTTCTTGTACCAAAACCGCCGTTACACCGATTTGTTCTTGATCGAGCGTAAAGCGGCTGCTATTCAGATAAATGTAGCGCCCTAATTAGAGAGGAGAATGACCATGCTATATGCAGTTAAAGGCAATACCCAGTTAAAGATTGATGAGGCCGAGCGTGCGGACTATCTGAAGCTGGGATATGACATTGCGGAGGTTGACGGGGATAAGCTGGCAACCGTCGAAACCTCACCAGCAAAGACAGTGCCTTATGCTGAACACAAAAAGGCTCTTGATGAAATCGAAGAGCTTAAGACACAGTTGGCCGATGCCAAGAAGTCAACAAAGAAGGAGGCTTAATCCATGGCAATCACCATAGCGGATATAAAAAAGCGTTCTATGCCAATCGGCAAGATCCGGGCGGTGATTCAGTACCTGGAAGAGAACCCGGCTGGTGGCGGTAGCGGATCGGTAACTTGGGCGAGTATTACAGGCAAACCTGCAGTAATTGCGGCTGGAGCGGATGCTGCTGCGGCACGGACGGCTATAGGTGCTGGCACACCATACACCTTGCCTGCTGCAACAGCATCCGTTATTGGTGGGGTCAAGCAGGCAGCGACACAGGCCAATAGTACGGCTACGGATGTGGCGGGGGTAGTAGCTGACCTTAATGCCATGTTAGCCAAGCTTAAAGCAGCTGGCATTATGGCGTAAGAAGGTGATCCCATGGCTTACGCAACAGTAGAGGAGTACGCACAGTATGGTGACGGCAGTATCCCAACAGAGGCGCTGCCTGCTGCCCTGGAGCGGGCCAGTGATCAGATTGACGCTCTGACCTATAACCGGATTGCAGCACGCGGCATGGCGGGTCTGACGGCCTTCCAGCGGCTAAAGGTGGTAAAAGCGGTCTGCCAGCAGGCAGAGTTCTATCATGCCTACGGTGATTACCTAACCTTTCCCTTGTCCGGTTACTCAGCCGGTAGCGTGTCGCTGTCGTTCAAGGCAATAGAGGGAGCAGGAGGCATCCAGACCACGGAAGCCGTGACGAGCCTCCTAGCCTCCACAGGGCTGACGAGCAGGAGGTTATGTTGATGATGCGTGGGAAGCTGCCGTTTCCAAAGTGGATATTAAAAACGCCTGTCGAAGTCTTCAGGACACGTACAAGCGAAGATGGGGAGCCTGTTGAAGAGTTAATCTTCAGCGGGCTTTGTTCATATGACGCTAGATCCAAACAGAAGCTGGACAAAGAGCGCCGCCTGGTGACGCTGGCCGGTAAAGTGATTATTCAAGGGGATATACTCCCCGGGGAACTGATCGAGGGGCTTGTGCGGATCGACGGGGCCGAGCGGAACATATTTAGCGCTTTACGCCCGCCGAACCCTGACGGCAGCGTGTTCAGCACGGAATTGGAGCTGATGTAATGGTCAAGGTCAAGACAAAGATGAATCCGCGGGCTATGCAGCGGCTGAGTGGCGCACCTGCCCGGGCGCTAGAGCTGACCATCCAGGGAGCCAAGGACAGTATATTGTCCGATATCATGGCCGCCGAGGTGGTGCCGAAGCAGACCGGGGAGCTGGAGCGCAGCGCGACAATCGACGCCAGCAAGTCCAAACGGGGCAAGGTAACAATCACCTATGATACGCCATACGCGCGTCGGCTTTATTGGCATCCGGAATACAGCTTTAGAAAAGATAAGAACCGGCACGCTCAAGGGGAATGGCTGCGGGCGTGGGCTGAAGGTAAGAAGACCCGGGGCGTGACTAAGGCCTTTAAGGAATTGCTGAAGAAGCTGGCAGGGGGATTTATCCGATGATGACACTGGCAGCGGTAAGGGATTGGTTGAAGACGCAGGTGGATTGCCAGAATTGGTACATCGGAAAGGCAGATACCAGTAAGCAGCAATGTATCAGCCTGTATAACATTAATAACGGTACGCCGGTACTGGCTATAGGCGGGCTGGATAATACCAGTTATGCGGTCAAAGCGGTATCCATACTGGTACATTGGAGTAAAAACGCAGATACGGCGGAGCGTAAGGCCCAGGAGGTCTATGCTGCGCTATTTGGGCAGTCTGCGGTCATTGGAGGTAAGCGGGTGATTAACTTCCAGCTGCGGACGCCTGAACCTGTCAGCGTGGGCACAGATGATGCTGGGATATACGAATACGTGATTGAGTTCACGATCTATTACGAAAGGTAGTGAGATTATGGCAGGAACAGGTGTTTTCCCCGTTCATAACAACGTTTTTAAAATCGGCATTAAGGGCCGCAGTTCCGCTGCTGCGGATATGGTTACCATTAAGGACCTGGAGAACTTCGCCCCGGCTATTGATGGTAACACGGAAGAGTGGTCTCCAATGGATCAGGGCGGTTGGACCCGTCGGGCGGTCACTGGTAAGGGCCTGACCATCAGCTTTAGTGGCAAACGTAACTACGGCGATCCTGGAAATGACTACGTTGCGGGGCTGATGATCGGGACCGGTCAGGAAGTTGAAACTAAATTTGAATGGACGATGCCAAGCGGTGCGAAGCTGACCATGGATTGTGTCATTAACTTGACCACTCCGGCCGGCGGCGATAGCACAAACATTGACGGTTTGGAATTTGAATTGTTGTCTGATGGTAAACCAACATTTTCACCGGCACCAGCCGGAGGAGGAGCATAATCAATGACAAACATTGTTAATATTACGGATAAATTCACCAAAGAAGATAAAGGTATACTCCAGATCGGGAATAAAAAGTACGAGATTGATAAGTCCGTTGAAGCTGTTATGCGCTTTGAAGAACTGGCCGATGATCAACGTGTTAAAGCGGTGGTTGCCGCACTCGAAGGAGCACTAGGCGAAAAAGCATCAAAAGAGATCGGGGTTAGAAAAATGGGCGCCGAAAACTTGAAGGTACTTTTGTCTGGAGTGACGGCCGCCATGCAAGGCATATCGTTTGAGGAAGTCGCTGCCCGATTTCAACAGCAGTAATCGAACAGAAAGCTGGTATGACTTGCGCGAGGATTGGCCTCTGGTGGAAGCGAGTTTGGCCAAACAGTATGGTATCCGTATTCGACAGCACGGGGACATGCCTTGGGACGAGTTTTGCTCTCTTATAGCTGGTCTGATGCCAGATACTCCACTGGGTAGCATCGTGACTATCCGCTCGGAGAAGGACCCGAAGGTGATTAAGTCTTTTAGCGCAGATCAGCGGCGGATATACAATGACTGGCGCAATCGTCAGGCTAAGCTAAAGCTACTGGATGAGGTTGCCCTGGATAATCAAATGAAGAGATTAGAGGCTACAATGGCCCGAATGTTCGGAGGTGGCGTGTAAATGGCAGGCAGTAGCGCAGGACGCATAGATTTAGATTTAGAGCTAAATTATGGAGCCTTCCAGCGCCAGCTCTCCGGCATAGCGGGTACGGCAAATGGTATGGTGGGAAGTGCATTTAAAGGCCTTGGCGGGATTATCGCTGGGGCCTTTGCTGTTGGTGGGCTGGTCCATTTCGGAAAGACGGCCATCGGACTGGCATCTGATCTGCAAGAAGTGCAAAACGTTGTAGATGTGACCTTTGGAGCAATGGCCCAGGACATTAATAACTGGTCCACAAGTCTGATCGATGATTTCGGGCTGTCGGAGCTGGCAGGAAAAAAATACGCCTCTACCATGGGTGCCATGCTTAAATCTTCCGGAATGACCGGGCTGCAAATGGAGCAAATGTCTAAGCAGTTGACAGAACTGTCGGCGGACATGGCCTCTTTTTATAACCTTTCCAATCAAGAAGCTTTTGAGAAGGTATTCAGTGGTATGACCGGGGAAACGGAGCCGCTGAAGGCGCTGGGGATTAATATGTCCGTGGCCAACATGGAAGCATACGCAATGTCCCAGGGCATTGATAAAGCGTGGAACAGTATGTCTCAACTGGAGCAGACCACTCTTCGGGCTAGTTACCTCATGAAGACCACAGCAGACGCCCAGGGCGACTTCGCCCGGACGTCAAATAGCTGGGCCAACCAGGTCAAGGTCATGGGAGAGCAGTGGCGAATTTTCCAGGGGACGATGGGCGCAGGCTTTATCAACATCCTGACTCCTGTCCTGCGCGGCCTGAACTGGCTGATTGCTAAGCTGCAGGTGGCCGCAGCCTACTTCAAGGCATTCACGGAGCTTATCTTTGGGAATGCTGCAGGCGGATCCTCTGGCGGTGTAGCCGCGCAGCCGATCAGTGACATGGGCACAGCTGCAGGAGACACGGCTGGTGCGCTGGGTGATCTGGGCGGCGCAGCTGATAAGACCGGCAAAAAGGCCAAGAAGGCAGGCAAGGATGTTAAGGGTAGCCTGGCTGGGTTTGACCAGCTCAATATTTTGGCGGACAGCGCCGCAGGTGCCCTGGATGATGCGGCGGGCAGTGTTGCTGGAGTTGGTGCTGGACTAGGCGCAGGTCTTGGGGGCGGCTTCGGGGACATCGATTTGGGGGCACCTGACATTAATGTAGACCCGATTAATGCAAAGGTAGCCGCATGGGTTGAGGGGTTGAAGGTTTCCTTTAATACTGCCCGAAAAGCTGTTTCTGACGCATGGGTTAATGTTCAGCCGTTGTTCCAGCCGTTAATAGATGCAATGACGCCTATCGACCAGTCTGTAACTAATATGGGTAATACGTTCCTACGTTTAATGAACGATGTGCTGAAACCGTTGGCTACTTACATTGTCGGTGATTTTATCCCTACAGTAGTAACGTCTACTCTTCAAAACTTTGTTCCGGTTTTCGCGGATGCACTTGTCGGAGCCTTTGATCTGGCGGATAAAACCTTTGCGAATCTCACCACAACTCTAACAGACCTGACAAATAGCACATGGTTGCCAAACATGGAAATCATGAAAAACGCATTGGTTTCAAATATGCCACTAATGGCAACGGCCGTGAATAGTCTTATCCAGGATACTTTGCTGCCAGCAGCGGACTTTTTCGCAAACGATTTTGTAATGCCGATATTTAAATCAGTGGTGGAAACTTTTGTTCCAGTTATCACAAATACGGCGGTAAACGCTGTTAACGTATTCACTAACACACTCACAAACTTTGCGGGGCGAGCCAAAGAGTTGTGGGAAGGCACCTTGATGCCGCAGTTTACTAGGCTGCGGGATGTAATTCTCGAAATAATGCCTCAGATCGGGGGAGCGGTTGACAAACTACTCAATGAAATCCTAATACCTTTTGTTGATTACGCGGTTAATGACTTCATCATGCCCATCGCTCAAAAGATCACAGAGGTTCTTGCTCCAGTATTTACTGACATACTGGTGACCGCGTTTCAGGAAGCGTCAAGCGCTTTTGAATGGGCAGTTGATATGATCGTAGATATTTACAATACGTTAATCAAACCCACATTTGATCTGATTAAACAGATCGTGCTTGATGTACTCGACATCATTAAAAAAGCTTGGGATGAACACGGGCAGAAGATTCTTGATGGGGTGAAGGAATTTCTGAATAACGTTAAAAATACCCTGAAAAAGCTATGGGATGAAGTGCTGAAGCCGATCATTGAACCGTTTTTGAAAACCATGAAAGAGCTGTGGGAAGGGACTATAAGCAAAATTATCGACAAAGTTGTTAACCTGGTAGCAAAGCTGATTGAGTCAGCACTGGAAATTTACAATGACTTTATCAGCCCTTTAATAAATTTCGTTATCGACCTACTGGCCCCGGCTTTCGTCAAAGGATTTAATATAGCCCTTAATATTGTCAAGACAGTTATCGAAGGTATAGGAGAATTCATATCTGGGTTACTGGATGCGCTTGACGGTTTGATCGATTTTGTCACGGGGGTATTCACGGGCAACTGGTCTAAGGCGTGGGAAGGAGTCAAGAAGATATTTAAGGGTGTATTTGACAGCCTTTGGGGTATCGTTAAGATTCCGCTGAACCTGATCATTGATGGCATCAACCATGTCATAGACGCTTTGAATAGTATTAGTATCGATATACCGGAAATTGATGTGTTTGGTAAGAAAGTTGGCGGCGGGAGTATTGGCATCAACCTGAATCATATACCTCCTCTGGCTAGGGGCGGTATCATCAGTACTCCTACCATCGCGCAGATCGGTGAACGGGGTACCGAAGCTGTGGTACCTTTGGAGAACACGCCGTTTGTCGATAAACTAGCCAGCGCTTTAGGTACTGCCGTACTGACTGCAATGCAGATGGGGCAAGCCTCAAGCAGTACGTCAGACCCATACTCACAACAGGAGACAACCCTACAAATCGACGGCGTAACCTTGGCGAGGGTATTGGCCCCGTACCTTGCACAAGAGAACAAACGTACGGGTAGCGCAATCATCCGAAACGTGACCACGGCCAGATAG

Protein sequences of DBSCAN-SWA_1

>NZ_LN831776|191776:225794|221250_221637_+|WP_039785130.1|DBSCAN-SWA
MTLAAVRDWLKTQVDCQNWYIGKADTSKQQCISLYNINNGTPVLAIGGLDNTSYAVKAVSILVHWSKNADTAERKAQEVYAALFGQSAVIGGKRVINFQLRTPEPVSVGTDDAGIYEYVIEFTIYYER
>NZ_LN831776|191776:225794|222380_222761_+|WP_081487073.1|DBSCAN-SWA
MRKSLPDFNSSNRTESWYDLREDWPLVEASLAKQYGIRIRQHGDMPWDEFCSLIAGLMPDTPLGSIVTIRSEKDPKVIKSFSADQRRIYNDWRNRQAKLKLLDEVALDNQMKRLEATMARMFGGGV
>NZ_LN831776|191776:225794|191776_194626_+|WP_046506247.1|DBSCAN-SWA
MITQEQLLDFMRETAYKPLTYDELVSHFALEDSESFKAFEELLLALEQDGRMILTRNARYGVPERMDLVRGRVQAHAKGFAFLIPDDRDHPDIYMNANDLKGAMNGDIVLVRITSRSPSGGRMEGEVVRIVKRGVLQTVGVFQSLENYGFVLPDDKRINRDIFIPKQSFKGAVDGEKVVVRIVNYPEGRAAAEGEIIEILGHKDDPGVDILSVIRKHQLPEAFPAEVMREAEQAPDSITEEEIIQQGRRDLRGLNIVTIDGADAKDLDDAVNVSRLENGHYKLGVHIADVGYYVREGSELDKEAFDRGCSVYLVDRVIPMLPHRLSNGICSLNPKVDRLTMSCEMEFDEHMKVVKHDVFTSVIRTKERMTYSDVRKIVEDEDPELLERYSPLIEDFRLMKELAMKLRGARMRRGAVDFDFEESKIIVDENGKAIDIVKRERSVAEQIIEEFMLAANETVAEHFHWLKVPFLYRIHEDPDPEKLQNFMAFAANFGYHVKGRGNSVHPRALQDLLEQIQGTKEQTVISTMMLRSMKQAKYDAESTGHFGLAAEFYSHFTSPIRRYPDLVIHRVMREVIENGGALTEKRHEYLASRMPEIAQQSSERERVAVEAERDTEQLKKAEFMQDKVGEEFDAMVSSVTSFGMFIELENTVEGLIRLSALSDDYYHFDEAHMALIGERTSKVFRIGDEVKIRVAKVNMDDHTIDFELVDMKPRAAGEHRSFGGRGGKGGRAGGGFAKPFGSKAGGKGRAGGKGKPGSAAGRGKAGGAAHAGKGKSGAAARAGEAPRAAEEASGGAPAGGRGKRGGGGPAEAARRAFAAVNRGEAGGAGTPRERDRSGGRGRGGEAGGSAGGRGISFGFGSGKGGYGAPAGEQISELRGVDASTRFRSREDLGSGAAANGGGGKSRRKKNKKGGVFISPSVTPGNVERSDKSGNPEGSGRRKKKKKTQE
>NZ_LN831776|191776:225794|219564_219798_+|WP_020425998.1|DBSCAN-SWA
MLYAVKGNTQLKIDEAERADYLKLGYDIAEVDGDKLATVETSPAKTVPYAEHKKALDEIEELKTQLADAKKSTKKEA
>NZ_LN831776|191776:225794|220164_220530_+|WP_020425738.1|DBSCAN-SWA
MAYATVEEYAQYGDGSIPTEALPAALERASDQIDALTYNRIAARGMAGLTAFQRLKVVKAVCQQAEFYHAYGDYLTFPLSGYSAGSVSLSFKAIEGAGGIQTTEAVTSLLASTGLTSRRLC
>NZ_LN831776|191776:225794|217706_217910_+|WP_141639038.1|DBSCAN-SWA
MMDYHDLIGERVKVVDKDGDVYIGPLITYEVGLDSDEDFDSIGIKTGEGYYESVPIPDIVSCEVLED
>NZ_LN831776|191776:225794|214649_216158_+|WP_020425905.1|capsid|DBSCAN-SWA
MGWFKNMVMKMLRINPAPESQIITIQEPYSYKANVLRNRLWYRGDPSELDQFYKQSVTDSVGKSRFWAAVPTAGLGIRKIHSGLPAMVADRLSDIVVADMDAITLKVQAETATWEKISEDNDFPELLAGAVTEALFVGDGAFKITVDPELSEYPLIEFYSGDQVEYKRTRGRLQEVIFWTDYTVSSKDYRLEETFGLGYIRSRLLDAYGKEVPLSVVPETAQLKPEITYDGDFIMAVPLMVFKSTKWPGRGKSLFDTKSDNFDALDEVVSQWMDAIRSGRVQKYIPEDMIPKNPETGELMRPNPFDNQFIRINSTFAEEAKGQINLVQPQILYEAFVASYASAVDMCLQGIISPSTLGIDLKKTDNAEAQREKEKATLYTRGKIVERLNEVIPQLVQTVLKVYDTMQSRAAGKYEASVTFGEYASPSFDAVVETVGKARTFGVMSIERAVEEMYGDTWTAEEKAEEVARLKAEQAPPTFDEPGANRDAPPGENEDDTGGEDE
>NZ_LN831776|191776:225794|201499_202837_+|WP_020426303.1|DBSCAN-SWA
MIKINKLEIENVKRVKAVKIEPTASGLTLVGGKNNQGKTSVLDAIAWALGGNKYRPSQAAREDSAIPPYLHLTLSNGLIVERKGKNSDLKVVDPNGQKGGQMLLDSFVEELAINLPKFMGSTNKEKANILLQIIGVGQQLHELEVKEQEVYNRRHAIGQIADQKAKFAKEQTYFPDAPKEPVSASDLIQQQQAILARNGENQLKRQRLTQFQALYANQGQEVERLKAMLADAEAKYAQTGVDLAAAQKDALQLHDESTAELETNIQQIDEINRKVRANLDKDKAETDASDYRQQYDALTTEINTVRQQKTDLLTNADLPLPGLTVENGELKYNGQCWDNMSGSDQLKVATAIVRRLKPECGFILLDKLEQMDMDTLQEFGAWLEQEGLQAIATRVSTGEECSIIIEDGYVAGQEGVTLQQLPGEIDPGDGWNEAVAPPTWKAGEF
>NZ_LN831776|191776:225794|195351_195831_+|WP_020427771.1|DBSCAN-SWA
MGKKADGKVLAQNKKASHDYFIEDTYEAGLVLTGTEIKSLRNGRANIGDAFATIRNGEIHVHNMHISPFEQGNRNNPSDPTRTRKLLMHKVQIHKLLGQSKQEGYSIVPLKIYVRNGYAKLLIGLGKGKKQYDKRDTAAKKDAQRDIQRALREKQKIAR
>NZ_LN831776|191776:225794|200182_200881_+|WP_020426306.1|DBSCAN-SWA
MGCDIHLFVEKRINGVWQVERGVNEPEIEEVRGFIDKSKERGESSAYWERLLEELRQGTMDYIYDGRHYLLFEVLAGVRAAHDLKPVSNPKGLPEDISPEAGESAESWGGDGHSHSWLTAAELLAYNWDQTITREGWVGVEQFKKYLEDGEPSMWSGGVGGGGTKYISNKEMKEGIRDGFLFGDPRQYYTLIHWNKSLRDALGKWCSWSLPKLAELAGDDPESARIVFWFDN
>NZ_LN831776|191776:225794|196346_197891_-|WP_020427772.1|DBSCAN-SWA
MPSTNKLIRAVAYPRYSSDNQREESIVAQMRAIEAYCQQKGYVLVNAYPDEEKTATTDRRPNFQRMIEDSNKKLFDVVIVHKLDRFARNRYDSAHYKRVLKRNGVRVESVLEHLDNSPESVILESVLEGMAEYYSLNLSREVRKGLRENAEQGTHTGGRPPYGLKVNPVTRMLEIDEQTYKAVQIYFDGIEADLSNDQIAAILNEKGYRTLNDRSFTSSSFATWGHNRKYKGDYTYDVSAPKDEDGKRNTNNKKPQEEQVLHEGRIPAIISSEQWDRVYRKLQDRKRKPGRMKAKVNYLLTGKIYCGACGALYSGNSYTNKKSSEGTVLTYYKCQDKCGNTSVRKDDIEAMVIQRLIEVCFSGEGIQEIIDKVQELYQKEKQQSVNDIEPIKRELAELEGKLKNWIEALGAGIKTVIENIKQAEQRKEALEYELDRAEVMQRVAVLDDTQIRSIIEMKKNLLLSGNEDEKKQVLQEYVDRVVIQPSSDINRFEAEITYRVFTNGAEGSRTPVRR
>NZ_LN831776|191776:225794|216154_217723_+|WP_046500875.1|DBSCAN-SWA
MRKYDIRGIYAQMEIDLIASMKRNLTRHENEEKKLGFKWPQWQQKKLEDLQQYKKEAAQIVKKAEPVIEQAVEQEIKGGFFAGIKRTAMKLLGKFMPLPRKLNIPDVSDENFFKLNEGRVNALVEATQGELKAARFAILRQSDDVFRQTIFKSQVYLNSGAASLGQAIDMATRDFLDKGLDYITYSNGRRVNVASYAEMALRASSQRAVFAGEGAKRQQMGNPFVVVSAHNNCSELCLPWQGKVYIDDVYSGGKASDGPYPLLSKAMAAGLFHPHCRHNMTTFVPGVSRMPEPVDNTEALANYKAEQRQRYMERQIRRYKRREAGSVDPDNQAAAAVKVKEWQGKLRNHLKTNEHLRRDPNREKILGGVSQAEHNELLKLAAKNAKIKETRAHIRSEAQPKKILTGQQNKHIPGTHEYKQYQAKYEKKGETGPSYLTIPPDQIEPLVKQYAGTGEIRLNNKGEWNHKETIMTNDAVIGKAVNNLTGAEADTTVFMIHYAKDGVHVVPAYPSLKKGKGNDGLS
>NZ_LN831776|191776:225794|200896_201148_+|WP_020426305.1|DBSCAN-SWA
MENQVKRKSIGEVLATIDPEKVNLQLVKPALMEVARSNTKRSGFLKIAVDDDVAVDCFQAMPDKIRFIISIDREDWNRAVVSE
>NZ_LN831776|191776:225794|201144_201507_+|WP_020426304.1|DBSCAN-SWA
MKAYDFQKAKLLIEQDREQIQEAALGMYEDWFWTAEEVFNDQEGFVRDLETVELIGGINESSWATPCLRITYRDGNESCIGCFKDDGSPSERGFVMPLGVLSGPAQDRMPPLTSKEGRHD
>NZ_LN831776|191776:225794|218670_219546_+|WP_020425997.1|DBSCAN-SWA
MPYNYVDSFLTVLQQKYTKELTSSGLTTQNAIFVNAKTIKIPRLDVAGYKNHSRAGGWNRQAVSNDFELKVLTFDRDVEFYVDAMDVDETNQIVSAANLTNVFETEQAIPELDKYRYSKIYADYVALGKTPDTTVITAANALQVFDQLMENMDEAEIPLEGRILYVTPAIYKLLKQAEDVQRFISVQSNNGTVDRSVRKLDDVTLVQVPSSRMKTIYDFTNGAVPGVGAKQINMILIHPSCVLAPIKHTAIYLWEPGSHTGGDGFLYQNRRYTDLFLIERKAAAIQINVAP
>NZ_LN831776|191776:225794|202836_203919_+|WP_046500864.1|DBSCAN-SWA
MQVITGKVQKAKKVVIYGPEGVGKSSLAAQFPRPIFIDTEGSTTEMDVARLPKPSSWEMLKQQVKWVWQGGQYGTLIIDTIDWAEMLCVESVCSTHQKNGIEDFGYGKGYIFVSEELGRMLNLLSDVVDAGIHVVLIAHAQIVKFEQPDEMGAYDRYQLKLGQKTASRTAPLVKEWADMVLFINYKTFSIATDKEGKKNKAQGGVRTVYATHHPAWDAKNRHGLPDEFPLDYGHIAHIFNTPAPTTNPSQQQQASVTPPQQSAQTVNQTGNIPNNIPAPVNTAPPTPSLNSNIPPALRELMTLHQVTESEIQQAVFQRNYYPVDTPIANYDPGFVEGVLVAAWSSVLGMIQNNRKAVPFN
>NZ_LN831776|191776:225794|203941_204556_+|WP_046500867.1|DBSCAN-SWA
MSEQERELGWDDTIEKDGGEFTLLPAGDYPFTVTKFERGRFNGSDKMPACNQAKIELTVHSQEHGDVVIFHNLFLHTKTEGLLSNFFAGIGQKRKGEKLKMNWQTVIGSKGRLKLEVNKFRGRDGEERTNNQVKSFYPADEQPAGQPPQQYQPQQQYQQPQQYQQPQYQQPQGGAAYNQPQYQQAPFPDSPPPQRGGNWSNGQF
>NZ_LN831776|191776:225794|213250_214645_+|WP_020425904.1|terminase|DBSCAN-SWA
MVDLTVIRRGARVELARREFFSFCQAMAPDFYRDDRQYLIDLCGELQEFYESTDDILVVNLPPRHGKSRTASMFAQWVFGKNLMEKVMTGSYNETLSTTFSKAVRDGIGTIKADENRIVYSDIFPQVRIKRGDGAMNLWSLEGGYNSYLATSPTGTATGFGATILMIDDLIKNAEEANNENVLEKHWEWFVNTMLSRLEEGGKIIIIMTRWATGDLAGRALEHFAEEHKRIRLLTMKALQDDGTMLCSDILSRASYEMKSRAMGEDIASANYQQIPIDIKGKLYSSFKTYTQLPTDGHDEPLFTGIYAYCDSADEGDDYLCNIIWGVYQKEAYVLDVIYTKQPMEITEPATAQALFAFKVNKARIESNNGGKAFARNIKRILETELKSNRTDVSWFHQSKNKTARIVSNATWVMQHIYFPVNWRDRWPDYYKAMTSYQREGKNAHDDAPDATTGVAETMFLLGG
>NZ_LN831776|191776:225794|211905_212415_-|WP_046500873.1|DBSCAN-SWA
MLTQNQQTNNSAFRSNFSNHNSSRIFGLTSASSYEVFPLPVNTSVQAPYSENYIPENVKDTNINTYWYNPSFADSLDIQFPDATNVSGLYITTHYEGGAPGVFYSFVVWGMKYGGAYDQVSEPVTYYVKNSQILTMPVIRLSKPGAFLTLKLEITSDQGFIAINDLKLL
>NZ_LN831776|191776:225794|199106_199271_+|WP_020426309.1|DBSCAN-SWA
MTINQQAESADHVWRRLELRRRRWQLLNGRLIVDEPEAAVWWLDKEIAEMEAGQ
>NZ_LN831776|191776:225794|198782_198986_+|WP_020426311.1|DBSCAN-SWA
MTHYSEFGAEARKVMLQKKIKMKDVASELGVSVTYVSEIFKGTRPGERQKPLIAKMLGMESEVVHES
>NZ_LN831776|191776:225794|221644_222103_+|WP_020425742.1|DBSCAN-SWA
MAGTGVFPVHNNVFKIGIKGRSSAAADMVTIKDLENFAPAIDGNTEEWSPMDQGGWTRRAVTGKGLTISFSGKRNYGDPGNDYVAGLMIGTGQEVETKFEWTMPSGAKLTMDCVINLTTPAGGDSTNIDGLEFELLSDGKPTFSPAPAGGGA
>NZ_LN831776|191776:225794|218052_218649_+|WP_020425996.1|DBSCAN-SWA
MEWLKELLKKAGVEESKVDGLIGDVNKELPKHFVPKSQYNELTDTKKKLEKDITDRDTQLEALSKDAGASETLKAEIARLQGENKTTKEKYEADLKDMTLNNAITAALNGKVHNEKVVTGLIDKNKLVIGDDGKVVGLDEQLTTLKTSDAYLFKPDEPGAGGGPGGFRVGGGGNGSGAGQATNEQLASIFGVADSKQF
>NZ_LN831776|191776:225794|209114_209519_+|WP_020425897.1|DBSCAN-SWA
MPTEFFMPMKPPTATHQEKQVAVVDGKPVFYEPDDLKAARAKLTAHLGKHVPQKKYSGVALRVTVKWLFPIPEGSKHYDGEWKKTKPDTHNLNKLPFDIMTNLGFWKDDALVASEIIEKFWAKLPGIYIKIEEL
>NZ_LN831776|191776:225794|222106_222415_+|WP_020425743.1|DBSCAN-SWA
MTNIVNITDKFTKEDKGILQIGNKKYEIDKSVEAVMRFEELADDQRVKAVVAALEGALGEKASKEIGVRKMGAENLKVLLSGVTAAMQGISFEEVAARFQQQ
>NZ_LN831776|191776:225794|222761_225794_+|WP_020425745.1|DBSCAN-SWA
MAGSSAGRIDLDLELNYGAFQRQLSGIAGTANGMVGSAFKGLGGIIAGAFAVGGLVHFGKTAIGLASDLQEVQNVVDVTFGAMAQDINNWSTSLIDDFGLSELAGKKYASTMGAMLKSSGMTGLQMEQMSKQLTELSADMASFYNLSNQEAFEKVFSGMTGETEPLKALGINMSVANMEAYAMSQGIDKAWNSMSQLEQTTLRASYLMKTTADAQGDFARTSNSWANQVKVMGEQWRIFQGTMGAGFINILTPVLRGLNWLIAKLQVAAAYFKAFTELIFGNAAGGSSGGVAAQPISDMGTAAGDTAGALGDLGGAADKTGKKAKKAGKDVKGSLAGFDQLNILADSAAGALDDAAGSVAGVGAGLGAGLGGGFGDIDLGAPDINVDPINAKVAAWVEGLKVSFNTARKAVSDAWVNVQPLFQPLIDAMTPIDQSVTNMGNTFLRLMNDVLKPLATYIVGDFIPTVVTSTLQNFVPVFADALVGAFDLADKTFANLTTTLTDLTNSTWLPNMEIMKNALVSNMPLMATAVNSLIQDTLLPAADFFANDFVMPIFKSVVETFVPVITNTAVNAVNVFTNTLTNFAGRAKELWEGTLMPQFTRLRDVILEIMPQIGGAVDKLLNEILIPFVDYAVNDFIMPIAQKITEVLAPVFTDILVTAFQEASSAFEWAVDMIVDIYNTLIKPTFDLIKQIVLDVLDIIKKAWDEHGQKILDGVKEFLNNVKNTLKKLWDEVLKPIIEPFLKTMKELWEGTISKIIDKVVNLVAKLIESALEIYNDFISPLINFVIDLLAPAFVKGFNIALNIVKTVIEGIGEFISGLLDALDGLIDFVTGVFTGNWSKAWEGVKKIFKGVFDSLWGIVKIPLNLIIDGINHVIDALNSISIDIPEIDVFGKKVGGGSIGINLNHIPPLARGGIISTPTIAQIGERGTEAVVPLENTPFVDKLASALGTAVLTAMQMGQASSSTSDPYSQQETTLQIDGVTLARVLAPYLAQENKRTGSAIIRNVTTAR
>NZ_LN831776|191776:225794|199267_199819_+|WP_020426308.1|DBSCAN-SWA
MKTLHFTYDPLRLVRIVLQRHVEETIQGRFYKAKQFACYEYLAKLSDEGLENLLQEYTKRHELEAITLADWRKDGKLIFDIIFEQPEYQQLEIDFKKRGYGITGLGVLDVESNTFYECGFAHHWQAIQNIIEKSYPRFHEPLQRMYFDETLTEHDGLTREELENFIMTNFELYGGTKPLQEYL
>NZ_LN831776|191776:225794|197914_198505_-|WP_052741400.1|DBSCAN-SWA
MEIVDNIKNLCYKNGTTIPKLEKELGFGNGTIYNWIKSSPSLEKLQKVASYFKVTIDDLVGWGHIYDLGSYIEDEREAQNVSLEDLSTAIQISPESLSQIENNKIPLTSELLGNITRYLGMTVQEFLIKYEMYEGAITQYYKGDINAYLDYLKHEEETVQINKPNIDEEDWTDKELEELKRFKEFLRMKRDHNTEK
>NZ_LN831776|191776:225794|204565_206146_+|WP_020426096.1|DBSCAN-SWA
MELRPYQQDSRESIQAEWEKGVRRTLLVLPTGCGKTIVFSKVIEDRVKLGERVLVLAHRGELLDQAADKLAKSTGLGCATEKAEQTSIGSWYRVVVGSVQTMMRDKRLQQFAADHFDTIIIDEAHHCLSDSYQRVLDYFKEANVLGVTATPDRGDMRNLGSYFESLAYEYTLPKAIKEGFLSPIKAMTIPLKLDLSTVGQQAGDFKSSDLGTALDPYLDSIAGEMWRVAKDRKIVVFLPLVKTSQKFTSILNAVGFRAAEVNGDSQDRAEILADYDAGKYNVLCNSMLLTEGWDCPSVDCIVVLRPTKVRSLYSQMVGRGTRLFPGKEELLLLDFLWHTERHELCHPAHLIAENEEVAQAMTQQIEQAGIALDLEKVEKQASEDVVAQREEALAKQLAEMKRRKAKLVDPLQFEMSIQAEDLSGYVPSFGWEMSPPSEAQVKTLEKLGILPEAIDNAGKATKLLERLDKRRSEGLTTPKQIRFLENRGFEHVGTWSFDHAKRLIDRIAGNGWRVPEGINPKEYRGE
>NZ_LN831776|191776:225794|212517_213258_+|WP_020425903.1|terminase|DBSCAN-SWA
MALTPKQKLFVQEYLIDLNATQAAIRAGYSPKTAEQQASRLLSNVKVQEAIREAQSHRAARTEITADMVLQRWWDIATADPNELIHLRRLACRYCHGKDHQYQWLDEEEYTQAVKDAIDSAESESKKQDRPVEAILPSEDGGYGFDRLADPHPKCPKCRGEGRADLHIEDTRKLKGGARLLYAGIKENKNGIEVIMQDQAKALENVARHLGMFVDKVQHSGNVDLNMNNPYKDLTTEELRKLARDG
>NZ_LN831776|191776:225794|199845_200118_+|WP_020426307.1|DBSCAN-SWA
MNEPVTKPLGWGMVAVMIDNPVVGGKQLHLFEAESTMSGAYVPPKQIKIDEVEKLRDFLIEQMPPDDLVNLLSTLEKAIHEKDDPSAATV
>NZ_LN831776|191776:225794|210025_211060_+|WP_020425901.1|DBSCAN-SWA
MSMIDRTNGSRVGYSGTSIPNQAIEYKSYGSGTVREYTLTPEELEEVRQKYPATKRDKAFKKPVAHNPREDRFPPKQQSQNTEEEQNMTGQRMSKEGPSSGLTKQIFLEQIASGETVASVEKAWGMKYNTLSFWVKKWDLRGINAVKAQELLAGESPRETQLLREKEALPPVGHQAGEVERLKAEVEHWKVQAAGWKKEKDAACEWGEEQRKKAVEAVALAGKAAEESMAKIERLTAARDGAIAAREAAELDLEQTETRCSQYAQSIDQLATECDGLQEEVNRLITERDDLVAEVEDLRDDIRRLREIQTLAAAPASDVHLLDRSIADLTRAKWILNRLTASGE
>NZ_LN831776|191776:225794|219801_220152_+|WP_082118060.1|DBSCAN-SWA
MAITIADIKKRSMPIGKIRAVIQYLEENPAGGGSGSVTWASITGKPAVIAAGADAAAARTAIGAGTPYTLPAATASVIGGVKQAATQANSTATDVAGVVADLNAMLAKLKAAGIMA
>NZ_LN831776|191776:225794|206591_208844_+|WP_020425896.1|DBSCAN-SWA
MFEKKLNLTTLLEHVDPSYLNYQEWVNVGMALKYEGYTASDWDEWSRRDGGRYHPGECFKKWTSFEGNGNPVTGATITQMAKDNGWLPRSAYDRELDWDDEISGSSGDYVVVDKNWIEGKEIHEPAEWNPVQQITTYIGALFEASENVGYVTEAWQSEEGKWLPNKGAYDRTAGELIELLHMCDGDIGQVFGDYKPEAGAWIRFNPLDGKGVKNENVTEFRYALVESDTMDIEKQNAVMRELELPIAVMVYSGGKSLHAIVRVEAANYDEYRKRVDYLYDICRRNGLAIDKQNRNPSRLSRMPGVERNGKKQFIVDTNLGKASWAEWHEWIEGINDDLPDPESLTESWDNMPPLAPPLIEGMLRQGHKMLMAGPSKAGKSFALIELSIAIAEGIKWLAWQCTKGKVLYVNLELDRASALHRFKDVYRALGMPPHNIGNIDIWNLRGKSVPMDKLAPKLIRRAAKKNYIAVIIDPIYKVLTGDENSADQMAHFTNQFDKIATELGASVIYCHHHSKGSQGGKKSMDRASGSGVFARDPDALIDLVELEVTEALYMQEENKAICSMYKGLFQQYNPAYLQEQVSQDDELSAKAMEDHAKRAMPHVMETIKPTIEQALEAVRARSAWRVEGTLREYAKFKPVNMWFQYPVHRVDDTGSLKDIEPEGESKPPWQKATGKRKNKAKEERRSKADEFADVVSNCNFGEPPTVLDVIAWYGSTGKEVAERTVRDWIKRYGYEIDRSLGFRIVKKEEE
>NZ_LN831776|191776:225794|209522_209747_+|WP_020425898.1|DBSCAN-SWA
MDYKALFWDVYLWTQQVNEAAARHGMQSPDFWQWVADSTGAICCKYNDHRLAIKQMLMMIEWLEEVYEQQRGRG
>NZ_LN831776|191776:225794|220858_221251_+|WP_020425740.1|DBSCAN-SWA
MVKVKTKMNPRAMQRLSGAPARALELTIQGAKDSILSDIMAAEVVPKQTGELERSATIDASKSKRGKVTITYDTPYARRLYWHPEYSFRKDKNRHAQGEWLRAWAEGKKTRGVTKAFKELLKKLAGGFIR
>NZ_LN831776|191776:225794|206192_206492_-|WP_046500869.1|DBSCAN-SWA
MNLIIQQYVHLKDKHKFRDSLTARKLYADVDFLPRIGDAIEDSVYHRNDPAYTVTEASFNYEENYYLAYLETVSIDSEDRNIIEERKEIYKAHGWEVLN
>NZ_LN831776|191776:225794|211081_211684_+|WP_020425902.1|DBSCAN-SWA
MTEQQVIDQLSSYRAKLARIQALGTYSIGSGIQISRLSEEDHLQQLHRRLRGLPSYMYLGKRDQELEATAHAYLTFYPAGVRAQRNAISDIGAYQEDDELLQELRAKIAKVIDARAGSKYDLDEVLDRLSELQDLQAEIKRIDDLLSLLEGYKPDYSRILYQDVISGRNWSEVAKEMALSKSVYFRWKKHAISAFIKLAE
>NZ_LN831776|191776:225794|220532_220859_+|WP_039785128.1|DBSCAN-SWA
MRGKLPFPKWILKTPVEVFRTRTSEDGEPVEELIFSGLCSYDARSKQKLDKERRLVTLAGKVIIQGDILPGELIEGLVRIDGAERNIFSALRPPNPDGSVFSTELELM

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_046506247.1|191776_194626_+	ribonuclease R	Q0GXV6	Lactococcus_phage	8.5e-87	38.3
WP_020427771.1|195351_195831_+	SsrA-binding protein SmpB	W5RAM5	Staphylococcus_phage	3.4e-41	53.2
WP_020427772.1|196346_197891_-	recombinase family protein	A0A0A7RTP8	Clostridium_phage	3.4e-66	33.7
WP_052741400.1|197914_198505_-	helix-turn-helix transcriptional regulator	A0A1C8E9A4	Bacillus_phage	7.6e-14	45.7
WP_020426311.1|198782_198986_+	helix-turn-helix transcriptional regulator	A0A0C5AJQ3	Paenibacillus_phage	2.3e-15	68.3
WP_020426309.1|199106_199271_+	hypothetical protein	NA	NA	NA	NA
WP_020426308.1|199267_199819_+	hypothetical protein	NA	NA	NA	NA
WP_020426307.1|199845_200118_+	hypothetical protein	NA	NA	NA	NA
WP_020426306.1|200182_200881_+	hypothetical protein	A0A2I7SC26	Paenibacillus_phage	7.2e-72	52.6
WP_020426305.1|200896_201148_+	hypothetical protein	NA	NA	NA	NA
WP_020426304.1|201144_201507_+	hypothetical protein	NA	NA	NA	NA
WP_020426303.1|201499_202837_+	AAA family ATPase	Q5YA97	Bacillus_phage	2.2e-162	67.9
WP_046500864.1|202836_203919_+	AAA family ATPase	A0A0K2CZH1	Paenibacillus_phage	1.3e-141	69.3
WP_046500867.1|203941_204556_+	hypothetical protein	A0A0K2CZ91	Paenibacillus_phage	3.0e-66	84.4
WP_020426096.1|204565_206146_+	DEAD/DEAH box helicase	A0A2I7SC38	Paenibacillus_phage	3.2e-277	89.2
WP_046500869.1|206192_206492_-	hypothetical protein	NA	NA	NA	NA
WP_020425896.1|206591_208844_+	AAA family ATPase	A0A0K2CZ75	Paenibacillus_phage	0.0e+00	81.3
WP_020425897.1|209114_209519_+	RusA family crossover junction endodeoxyribonuclease	Q5YA86	Bacillus_phage	4.6e-47	70.7
WP_020425898.1|209522_209747_+	hypothetical protein	A0A2I7SC31	Paenibacillus_phage	9.2e-21	56.8
WP_020425901.1|210025_211060_+	hypothetical protein	NA	NA	NA	NA
WP_020425902.1|211081_211684_+	hypothetical protein	NA	NA	NA	NA
WP_046500873.1|211905_212415_-	hypothetical protein	NA	NA	NA	NA
WP_020425903.1|212517_213258_+|terminase	terminase small subunit	I6X6R5	Burkholderia_virus	5.7e-51	47.5
WP_020425904.1|213250_214645_+|terminase	phage terminase large subunit	A0A090EUA8	Clostridium_phage	2.5e-185	67.4
WP_020425905.1|214649_216158_+|capsid	phage capsid protein	M9Q246	Clostridium_phage	6.1e-169	59.7
WP_046500875.1|216154_217723_+	hypothetical protein	M9Q2F2	Clostridium_phage	1.5e-93	46.2
WP_141639038.1|217706_217910_+	hypothetical protein	NA	NA	NA	NA
WP_020425996.1|218052_218649_+	hypothetical protein	A0A090DBQ0	Clostridium_phage	1.3e-08	28.0
WP_020425997.1|218670_219546_+	hypothetical protein	M9Q2F4	Clostridium_phage	1.1e-80	53.2
WP_020425998.1|219564_219798_+	hypothetical protein	NA	NA	NA	NA
WP_082118060.1|219801_220152_+	hypothetical protein	A0A2H4YGU5	Raoultella_phage	7.6e-14	53.1
WP_020425738.1|220164_220530_+	hypothetical protein	M9Q2K9	Clostridium_phage	2.4e-18	47.9
WP_039785128.1|220532_220859_+	hypothetical protein	M9Q2I3	Clostridium_phage	1.5e-32	61.0
WP_020425740.1|220858_221251_+	hypothetical protein	M9Q249	Clostridium_phage	4.5e-23	46.9
WP_039785130.1|221250_221637_+	hypothetical protein	M9Q2F6	Clostridium_phage	6.8e-40	59.4
WP_020425742.1|221644_222103_+	hypothetical protein	O03972	Lactobacillus_phage	4.2e-12	30.7
WP_020425743.1|222106_222415_+	hypothetical protein	NA	NA	NA	NA
WP_081487073.1|222380_222761_+	hypothetical protein	M9Q2I4	Clostridium_phage	3.8e-27	47.5
WP_020425745.1|222761_225794_+	hypothetical protein	A0A2H4J4V9	uncultured_Caudovirales_phage	5.0e-45	40.3

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_LN831776|879985:891647|DBSCAN-SWA
TATGATCGAACGTTACAGCAGACCTGAGATGCGGGCCATTTGGACCGAAGAGAATAAATTCAACGCATGGTTGGAAGTGGAGCTTTGCGCCTGCGAGGCATGGGCCGAGCTGGGAGTCATCCCGCATGAAGATGCTGCGAAGCTGCGGAAGAATGCCAAATTCGACATCGGCCGCATTAATGAAATTGAGCTCGAAACGCGTCATGATGTTATTGCGTTTACCCGTGCGGTATCCGAGAGCCTGGGCGCGGAGCGCAAATGGGTGCATTACGGATTAACCTCGACGGACGTTGTGGATACGGCGCTCGGCTATCTGCTGCGCCAGGCCAACGAGATTCTGGAGAAGGATATTATCAACTTCATCGAAATTCTCAAAGACAAGGCGCTTGCCTACAAAGATACTCCAATGATGGGACGCACCCATGGCGTGCACGCCGAGCCAACGACATTTGGACTCAAAATGGCGCTCTGGTACGAGGAAATGAAGCGCAACCTGGAGCGTTTCCGCCATGCTGCAAACGGCGTGCAGTTCGGCAAAATCTCCGGGGCGGTCGGCACCTACGCCAATATAGACCCGTTCGTTGAAGAATTCGTCTGCCGCAAGCTGGGCACCAGCCCGGCGCCGATCTCCACACAGACGCTGCAGCGTGACCGCCACGCGGAATATATGGCTGCGCTGGCCCTTGTCGCCACTTCCCTGGACAAGTTCGCTACCGAAATCCGCGCGCTGCAAAAGAGCGAAATCCGCGAGGTGGAAGAGGCTTTTGCCAAAGGCCAGAAGGGCTCGTCGGCGATGCCGCACAAACGCAATCCGATCGGCTGCGAGAATATCTCCGGCTTGTCGCGCGTGATTCGCGGCCACATGATGACGGCCTACGAGAACGTGCCGCTGTGGCATGAGCGCGACATCTCGCATTCCTCCGTGGAGCGGATTATCCTGCCGGATGCGACCATGCTGCTGAACTATATGCTGAACCGCTTCGGCAACATCGTGAAGAACCTGACCGTGTTCCCGGACAATATGAAACGCAACATGAACCGCACCTTCGGGGTGCCGTTCTCCGGCCGCATTCTGACCAAGCTGATCGACAAGGGCTTCAGCCGTGAACAGGCCTACGATACCGTACAGCCGCGTGCGATGCAGGCCTGGGAGGAGCAAACCCAGTTCCGCGATATCGTAGAGGCTACCCCGGAGATCACCGCTGTGCTTAGCCCGGAAGAGATTGAGGATGCTTTTAATCCTTCGTGGCACCTTAAGCATGTAGATACCATCTTCCGCAAGCTGGAGCTAATTTAATAAAAGGTAAGTTAGTGGTGAACTAAGGAACGCAGCAATAGATGGCGTAAGGACCAGGAGAGCGGGGGTTCTGAATCGAGCACAACTGGAAGCTTGAATATATTGGTTCGGTAAAAGAGGAGCGGAGAGAAATTTTGGAACTGGAGAAGCGTTAGCGTTCGCCTTTATGGTCGGGCTTCTACCGCAGCTTGCGGTTAAATCAGAGAAATATGACCATAACAGCGATCGGAAGTCCAAACATTTCTTGCAGTGAAACTTATTTACCAGACCGTTGTGGGAGCTTTTGATTGAGCGGTGAAGATCCGCGCCTAATATTGTTCTTTACGCAGAGTATACGCAAGATCATTTGTTCAAGGGAGGAAAGGTCATGACATACCCTGCCGTATCCACGGCTGTGGATCTCGTAAATGCACCGCTGCTCTACAAAGGAAAGGTTCGCGAGCTGTACGATCTGGGGGAAGAAGTGCTGATCGTGGTCACGGACCGGATATCCGCATTCGACTATGTGCTTGATCCGGCGGTGCCGGAGAAAGGCAATGTGCTTAACCGGCTAAGCGCGTTCTGGTTTGGCCAAACCAGTGAATTGATGGAGAACCACGTCGTGCATATTGATGTGGACCGGCTGGGGGGGATCGTGAAGGACCGGGAGGCGCTCAGAAACCGTATCATGGTCGTCCGCAAAGCGGAGCGTATTGACATCGAATGCGTCGTGCGCGGCTGCATTACCGGCGGCGGCTGGCGGCAGTATCAGGAGACCGGCAAGGTCAACGGCATCGGGCTTCCTGCGGGCCTGCGCAAAAACGCGCAGCTGTCCCAGCCGATTTTTACCCCTGCGGCCAAAAATGATGTCGGCCACGACGAGGATATCCCTTTTGAGAAGATGCAGGAGCTAATTGGGGCGGAGCTTGCGCTGGAGCTTAAGGAGAAAAGCCTGAAGCTGTTCGCTTTTGCCAGAGAGTACTGCGAAGAGCGTGGCATTATCCTCGCGGATTGCAAATTCGAGTTCGGACTGCTGGACGGCAAGGTGATCCTGATCGACGAAATTTTTACCCCGGATGCTTCACGCTTCTGGGCCAAGGACAAATATGCGCTGGATATTGAGATCGACAGCATGGATAAGGAGCCGGTCCGGACGTATCTGTCCGCATCCTCCTGGGACAAGAACAGCACCCCGGACCCGCTCCCGGCAGAAGTCGTGGAAGAAACCACCCGCCGTTATCTGGACATTTATCATCGCCTCACCGGCAAGACTTTATAGATTGTTGTATTATCCCGGCCAGTATTAATTGCACTCTATGCAGTTATTTTGCACAAAATAAATGCAACTTGCATTTTAAATGTACTTGGTACAGCTGAAACAGGTGATAAGGCCTTAAAAAGCAGATATTCAGGAATATAACTGTAAGGAATACAACTAAAAATGATTTTGCCGGAGATATTGAGATTATAGCTGTATGTTATGCAGTAAAAGCTGTATGCCAAGCAGTTGAGTTAGTTATAACGTTGAGGTACCGACCATTAATCATGCCAAGCCAAGCTCATTAAATTTTAGGAGGAACTACAAGCGTATGTTAAAAGCGACAGTGTATGTCACCATCAAAAAAAGTGTGCTCGATCCCCAGGGTGTAGCCGTGCAAGGGGCGCTGCATTCCGTTGGTTTTCAGGAAGTGGAGAGCTTGCGCATTGGCAAGTATATGGAATTGACCCTGGATACCGACAACCGCGCTGAAGCGGAAGGACGCCTGAAGGAAATGTGTGAAAAGCTGTTGGCCAACACGGTAATCGAGGATTACCGCTACGAATTGGAGGACTAAAAGTCATGAAATTTGCTGTACTTGTCTTTCCGGGTTCCAATTGCGATATTGACTGCTACAAGGCGGTAGAAGACAGCCTCGGCGAACCAGTAGAATATGTGTGGCATACGGCGACTGATCTGTCGGCTTATGACTGTATTCTTGTGCCGGGCGGCTTCTCTTATGGTGATTATTTGCGCTGCGGTGCGATTTCCCGGTTTGCTCCGGTGATGGCTGAAGTGGCCAAGGCCGCAGAGCAGGGCAAATTTGTGCTCGGCATCTGTAACGGATTCCAGATTCTGACCGAAGCCGGCCTGCTGCCAGGTGCACTGCGCCGCAATATGTCGATGAAGTTCCGCTGTCATGATACGGTGCTTAAGGTGGTTAATAACACTACGCCGTTTACAGTTGATTATGCGAAGGATGAGGAGATTGTCATTCCAATCGCGCATGGTGAAGGCAACTACTACTGTGATGAAGAGACGTTGGCCGGGCTAAAAGCCAATAATCAGATCGTATTCACCTATAGTGATAATCCTAATGGCTCCGTGGAGCATATTGCCGGGATTTGCAATGTGCAGGGCAATGTGGTTGGCATGATGCCTCACCCGGAACGCGCAGCGAACAGCCTGCTTGGTTCGGAAGACGGCAAACGGATGTTCACATCCATTCTCAAGACATGGAGGGATCGTTATGACACAGCAAGTATCCGCTAAGGAGCCGACCGCCGAGCAAATCGCGGAGCAGAAAATCTACAATCAATTCGGTGTGTCGGACAGCGAATATGAGCTCATCACTTCTTTCATGGGCCGCAAGCCAAACTATACGGAGATCGGCGTGTTCAGTGTAATGTGGTCTGAGCACTGTGCCTATAAGAACTCGAAGCCGCTGCTGGGCCGTTTCCCTACGAGCGGGCCGCGCGTGCTGATGGGACCGGGCGAAGGCGCCGGGATCGTTGATATCGGAGACAACCAGGCCGTTGTTTTCAAAATCGAAAGCCATAACCATCCTTCGGCAGTTGAGCCTTACCAGGGCGCGGCGACCGGGGTGGGCGGGATTATCCGCGATATTTTCTCCATGGGTGCAAGACCGGTGGCGCTGATGAACTCCCTGCGTTTCGGAAAGCTCGAAAGCGACCGGGTCAAATATTTGTTCGAGCATGTCGTATCCGGTATCGCCGGCTATGGCAACTGTATCGGGATTCCGACAGTGGGCGGCGAAATTATGTTCGACAACAGCTATGACGGCAATCCGCTGGTCAATGCCATGTGTGTCGGACTCATTGATCATGACAAAATCCAGCGCGGTGTAGCCAAAGGTGTAGGCAACCCGGTGTTCTACGTAGGTCCTCCTACCGGACGCGACGGGATTCATGGCGCAACCTTTGCCTCCGTCGAGCTGAGCGAGGAATCGGAAGCCAAGAAGACAGCGGTGCAGGTCGGCGATCCGTTTATGGAAAAGCTGGTGATGGAATCCTGCTTGGAGCTGATCGACAGCGGCATCGTGCTGGGCATTCAGGATATGGGCGCAGCGGGGCTTACCTGCTCCAGTGCCGAAATGGCGAGCAAAGCGGGCAACGGCCTGGAACTGTATCTGGACCAGGTGCCGCAGCGTGAAGACGGCATGACGCCTTACGAGATGATGTTGTCCGAGTCGCAGGAGCGGATGCTGTTTGTGGTTGAACCCAAGGATGAAGCGCAGGCACAGGAGATTTTTGACCGCTGGGGGGTTATCTGCCGTAAAGTGGGCAAGGTAACCGATGACGGCCGCCTGAAGCTGTTCCATCATGGCGAGGTTGTCGGTGATATGCCGGTAAAGGCTCTGGTGGATGAGTGCCCGATTTATAAAAAGCCATCTGCGGTGCCGGCGTACTATGAAGAGAATGCTTCGGTTGATACGCTTCGTTATGCAGAAGTAAAGGATCTGGGCGGCGCCTTGCATACCGTATTGGCATCACCGACAGTAGCGAGCAAAGCATGGGTCTACAACCAGTACGATTACATGGTGCGGACAAGCACTGCGGTCCGTCCCGGCTCCGATGCGGCGGTGGTGACGATTCATGGCACACGCAAGGGCTTGGCTATGACTACAGACTGCAATGGCCGTTATGTCTATCTGGACCCTGAAGTTGGCGGGCGGATTGCAGTCAGCGAAGCGGCGCGCAACATCGTCTGTTCCGGGGCCAAGCCGCTGGCAATTACGGATAACCTGAATTTCGGCAGTCCGGAGAAGCCGGAAATATTCTGGCAGATGGAACGTGCCGTAGATGGCATGGCTGAAGCCTGCCGCGTGCTGGACACGCCGGTTATCGGCGGCAATGTCAGCTTGTACAACGAAAATGCTTCTGGAGCAATCTATCCGACACCGGTTGTCGGTATGGTCGGGCTAGTCGAAGATACCGATCATATTACCACTCAGGCCTTCAAGCAGGAAGGCGATGCTATTCTGCTGCTGGGCGTGACTAAGGCGGAGCTGGGCGGCAGCGAATTCCAATATGCCGTACACGGCCTGACGGAAGGCCGTCCGCCTGAGCTGGATCTGGCAACCGAGCAGAAGCTGCTGGATGCTGTTCTTGCGGCGATCCGCAGCGGACTGGTCCGCTCGGCGCATGACCTCTCCGAAGGGGGCTTGGCCGCAGCGCTGGCTGAGAGCTGTATCAGCGGCTCTATCGGAGCTAATGTGGAATGGTCCGCTGGCGGACTGCGCAGAGATGTGGCGCTGTTCAGCGAGAGCCAATCCCGCATTGTGCTGACAGCGGCACCTGGCCGAGCGGAAGAGCTGAGGGCAGCAGTAGCTGCCTATGGCGTGCCGGCTGAAATTATCGGAACGGTCGGCGGCGACAGACTGCGCGTCTCCTTGGACGGCGAAGCCGTGCTGGACGAGGCTGTAGCCGCATTAAAAACCACTTGGGAGGATGCTATTCCATGTCTTATGAAATAAAGACCGGGAACAAGCAGGAGAACCCCATCCTGTGGACCGGCGACTTTTACAACGAAGGAACGGGCTCGGGAGATATTTTTGATACGCTAAAAGAAGAATGCGGCGTCTTCGGGGTCTTCGGACACCCGGAGGCTGCCTCCATGTCATATTACGGCCTGCATGCCCTGCAGCACCGGGGGGAAGAGAGTGCGGGCATCTGCGTGGCAGATGGACGGGATTTCCACTATCACCGCGGCATGGGGCTGGTCAAGGAAGTGTTTGATAAGGACAAAATCGCTTCGCTGGTCGGCAACATGTCCATTGGCCATGTGCGCTATTCCACCAGCGGTGACAGCCGTCTGACCAATGCGCAGCCGCTGGTTTTCAAATACCGTGACGGGGATTTGGCGATTGCCACCAACGGGAATATTGTGAATGAGCCGCTGATCCGCAAGCAGCTGGAGCAGAGCGGCTCCATCTTCCAGACCACAAGCGATACCGAGGTGCTGGCGCATCTGATTGCCCGCTCGCAGAAGGAGTTTGTTGAGGCGACTAAAGATGCCCTCCAGCAGCTGGTGGGCGGCTTCGCCTTCCTGCTGATGACCAATGACAAGCTGATCGTAGCTTCCGACACGCATGGCCTCCGTCCGCTGGTGATGGGGCGTGTAGGTGAAGCCTATGTTTTTGCCTCGGAATCCTGCGCGCTGGAAGTCATCGGCGCTCAGTTCGTCCGCGACATTGAGCCCGGCGAGCTGCTGGTGCTTGACCAGAACGGCTTCCGGGAAGACCGTTTTGCCGAGCCGCAGCGCAAGGCGTTGTGTGCGATGGAATACATTTATTTTGCCCGGCCGGACAGCGATCTGAACGGCTCCAACCTTCATGCCGCCCGCAAACGGATGGGCAGCCGGATGGCGCTGGAAGCCTTCGTTGACGCTGACATCGTAACCGGCGTGCCGGATTCCAGCATCTCTGCGGCTATCGGCTATGCCGAGCAGACTGGCATTCCCTATGAGCTTGGCCTGATTAAGAACAAATACACCGGCCGCACCTTCATCCAGCCGAGCCAGGAACTGCGCGAGCAAGGCGTGAAGATGAAGCTGAGCGCGGTGCGCCGCGTCGTAGAAGGCCAGCGCGTGGTTATGATCGACGACTCCATCGTGCGCGGCACCACTTCGCGCCGGATCGTCAATCTGCTGCGCGAAGCCGGAGCAACTGAGGTCCATGTGCGGATTACCTCGCCGCCTTTCAAGAATCCTTGCTTCTACGGCATCGATACTCCGGACCGCCGCGAGCTGATCGCCTCTTACAAGACCGTCGAAGAAATCTGCCACGAGATCAATGCCGATTCGCTGGCATTCCTCACGCCGGCAGGCCTGATCCAGGCCATCGGCGGTTACAACAGCGGAGATTATAAGGGCGGCCTGTGTCTGTCCTGCTTCGATAATGATTATCCGACGCAGGTGGATTTTGGCGGGGAGGAGAAGGACGGGTGCAGCTGCTGAGGCAGCCTATCATCTCCCTAAGTCGTGGGTCCATCCCCCTAAGTCCCCCTTGCAAAGGGGGATTCCAGAGGGCGCTGCCCTCCGGCCACCCGAAAGCTCGGCGGTAGGAGTTTGCTCTAAACTTGCTAAGAGGACGTGGGTGCGGGGGCCCGCTTTGTCCTGCGGACACGCTTTACGGCGCACCGCGCCCTGGCGGCATGCTGCCCCGCCGGGCCTGAATGCTCAAGAACCAGCCTGTTTGCTGCGCAAAAGCGGGGGTTCTCTCGCCCTAAGGCGCGCACGGCTTCGCCCCGTGCGCCAAGGGCAAAAGCTTGAGTCCCCGTTCTGTTTGCTGCGCAAAAGCGGGGGAGCTCTCGCTAAAGGAGGCGCTTGGCTTCGCCAAAAGCGCCGGCTGACTGCCCTGTGCAAGGCGCGTAACTGCGGCTTGCGGCGGGGGTTGAACCCGGTGGTTGGAGTTATGGAGAGGAAGTTTGGAACTGGAGGAGCGATAGCGTTCGCCTTTATGTTTGGATTTCTACCGCGGACAGCGGTTTAAATCAAGGAAATCCAAACATAACAGCGACCGGAAGTCCAAACATTCCTCGTAATGACGACTATAACCACCACGCTTCAAATCCCTGCCGCCCCGAACACACGCGCTCTAAACTAATTCAAATGAGGTGTCCAATAGTGTCGGAAGCTTATAAAAACGCCGGAGTGGATATTGCAGCTGGCAATGAAGCGGTAGAACGCATGAAGAAGCATGTGAAGCGCACATTCCGTCCGGAAGTGATGACAGAGCTCGGCGGGTTCGGTGCACTCTTCGGACTCAATAAAGACAAGTATGAAGAGCCGGTGCTCGTATCGGGAACCGACGGGGTGGGCACGAAGCTCAAAATCGCTTTCGCGGCCGACCGCCACGACACGATTGGCATCGATGCGGTAGCCATGTGTGTGAATGATATTGTGGTGCAGGGGGCAGAGCCTCTGTTCTTCCTTGATTATCTGGCCTGCGACAAGGTTGTGCCCGAAAAGATCGAAGCGATTGTTGCCGGGATTGCCGAAGGCTGTCATCAGGCAGGCTGCGCGCTGATCGGCGGCGAGACGGCTGAGATGCCGGGCATGTATTCGGCGGGTGAATATGATATCGCCGGATTCACGGTGGGTGTAGCCGACAAGGCCAAGCTGGTGACAGGTGCGGATATCGCGCCTGGAGATACGGTCATTGGCCTGGCGTCCAGCGGTGTGCACAGCAACGGCTTTTCGCTGGTGCGCAAGCTTTTGCTGGAGGAAGACGGCTATGGGCTGAACGATGTGGTGCCGGAGCTGGGCGCTCCGCTGGTAGATGTGCTGCTGGCGCCTACCAAGATTTATGTGAAGCCGCTGCTGGGGCTGCTGGAGCAGCTGCCGGTCAAGGGCATGGCCCATATTACCGGAGGCGGGTTCATTGAGAACATTCCGCGCGTGCTGCCGGAAGGTGTGAACGTGGACATTAACTACGGCTCGTGGCCGGTTTTGCCGATCTTTGATTTGCTGCAGAAAAAAGGCGGAGTCAGCAACCGTGATATGTTCACCACCTTTAATATGGGCGTAGGTCTGGTGCTGGTTGTGGCTGAGGCGGATGGAGAACGCGCACTGGAATTGTTAAAAGCGGCCGGGGAAGAAGCCTATTTGATTGGCAGAGTAACGGAAGGGGAACGCATCGTTACCTTTACGGGAGCTGAAGTGTGATGCAGTGGAGCCGGATCGCTGTCTTTGCCTCCGGGCAGGGCAGCAATTTTGCCGCACTGGCAGAAGCCGAGCGGGCAGGACAGCTTGGCGGAGGGCGTATAGAGCTGCTGGTATCCGACAGGCCGGAAGCGCCTGTGGCGAAACGTGCGGAGGAGGCGGGCATCCCCGCTCTGATGCTGCGGCCGAAGGACTTCGCAAGCCGCGAGCTCTACGAGGCTGAGATCGTAGCCGAGCTGCAGCGCCGGGATATCGGCCTGATCGTTCTGGCCGGATATATGCGGCTGATTACCCCAGTGCTGCTGACGCCTTACGCAGGCCGGACCGTGAATATCCACCCCTCGCTTTTACCCGCCTTCGCCGGGAAGGACGCCATTGACCAAGCGCTGGATTACGGTGTGAAGCTGACGGGAGTAACGGTGCATTTTGTCGATGGCGGCATGGATACCGGACCGGTTATTGCCCAGCGCAGCGTGGCCGTGGAGCCTGGTGACACTGTGGAATCGCTGGCAGAGCGCATTCATCAAGTGGAATATGAGCTGTATCCTGAGGTTGTGCGTGCTTTGGCTGAAGGAAAGGTAGAACTGGATGGCAGAAAAACGGTTATTCGGGAATAGCCGCCCGGTTCTGATATTTCTCGGGAAATATTGCACAAGCAGTGAAGGCAGCCCGGAAGAAGGCGGATTTTGTTCTTTTTTTGCACAGTTGGTGTTGAAATAAACGGAGATTGTACACCGTCCCTCGCAGCTGCATTGAGGTTGGTAAACCATTTTACTCAATTAGGTTAGTATCGGCACAACGAAGATTACAGATTTCAGGTTCAATCTATATAGCAGATTTTCTCAGTACGCTTCACCTGCAACTAAATTTAACACCATCCGGAGGAGGACTATCAAAGTGAGTATCAAAAGAGCGCTGGTCAGCGTATCGGACAAACAGGGCATCGTGGATTTTTGCCGCGGGTTGTCTGCATTGGGCGTAGAAATCATCTCCACAGGCGGCACTAGCACCCTTTTGGCAAAAGAAGGCGTACCGGTCATCGGTATTTCGGATGTGACAGGGTTCCCGGAAATTATGGACGGACGCGTGAAGACGCTGCATCCGGCCGTACACAGCGGCCTTCTGGCGGTCCGTGACAACGAGGAGCACACTCGGCAGATGCAGGAGCTGGGCCTGGACTACATCGATCTGGTTGTCGTGAATCTCTATCCGTTCGCGGAGACGATTGCCAAAGCGGATGTGTCGTATGAGGAAGCGATCGAGAACATCGATATCGGCGGACCGACGATGCTGCGTTCGGCGGCGAAGAACCATGCTTTTGTCAGTGTGGTCGTGGATGCAGCCGACTATGCCACGGTGCTTGAGGAAGTGCGTGCAGGCGGAGATACCACTCTGGAAACCCGCAAACGTCTTGCGGCAAAAGTGTTCCGCCACACGGCGGCTTACGATGCCCTGATTTCCGATTATCTGGCGAATGTGACCGGTGAACCGCTGCCGGAGCGCTATACGGTAACTTACGAGAAAATTCAGGATCTGCGGTATGGGGAGAATCCGCACCAGAAAGCAGCGTTCTACCGCAAACCTCTGGCTGCCCAGGACACCCTCACATCTGCTGAGCAGCTGCACGGCAAGGAACTGTCCTACAACAACATCAATGACGCCAACGCGGCGCTGCAGATCGTGAAGGAGTTCGAAGAGCCGGCTGTGGTAGCCGTTAAGCACATGAATCCTTGCGGGGTAGGCGTAGGGGCAAGTGTATATGAAGCGTATCAAAAAGCCTATAATGCCGATCCAACCTCCATCTTTGGCGGAATCGTAGCGGCCAACCGGATTATTGATGCCGATACGGCCAATATGCTGAAGGACATCTTCCTGGAAATCGTGCTGGCACCGGGCTTCACAGAGGAAGCGCTGGACATTCTCACGAAGAAAAAGAATATCCGCCTGCTCAAACTGGGCAATCTCAGCACGGCTGCGGCGCGGAAATCCAGCTTTGTGGTAACTTCCATTGAAGGCGGCATGGTCGTTCAGGAGAGCGATGTGCACTCCGTCAATCCGGAAGAGCTGCAGGTGGTGACGAACCGCAAGCCTACTGAAGAAGAGTTGAAGCAGCTGCTGTTCGGCTGGAAGGTAGTTAAGCATGTGAAGTCTAACGCTATCGTGCTGGCGGCGGATGATATGACAGTCGGCGTAGGTGCAGGCCAGATGAACCGTGTCGGTGCGGCGAAGATCGCCATTGAGCAGGCCGGGGAGAAAGCCAAGGGTTCTGTGCTGGCCTCCGATGCGTTTTTCCCAATGGGCGATACGCTGGAAATGGCGGCAAAAGCCGGCATCACGGCGGTTATTCAGCCGGGCGGCTCCATCAAGGACGAAGAGTCCATCAAAGTTGCTAATGAATATGGTATTGCCATGGTCTTCACCGGCGTTCGCCATTTCAAACACTAG

Protein sequences of DBSCAN-SWA_2

>NZ_LN831776|879985:891647|883100_883790_+|WP_020430568.1|DBSCAN-SWA
MKFAVLVFPGSNCDIDCYKAVEDSLGEPVEYVWHTATDLSAYDCILVPGGFSYGDYLRCGAISRFAPVMAEVAKAAEQGKFVLGICNGFQILTEAGLLPGALRRNMSMKFRCHDTVLKVVNNTTPFTVDYAKDEEIVIPIAHGEGNYYCDEETLAGLKANNQIVFTYSDNPNGSVEHIAGICNVQGNVVGMMPHPERAANSLLGSEDGKRMFTSILKTWRDRYDTASIR
>NZ_LN831776|879985:891647|888164_889205_+|WP_020430577.1|DBSCAN-SWA
MSEAYKNAGVDIAAGNEAVERMKKHVKRTFRPEVMTELGGFGALFGLNKDKYEEPVLVSGTDGVGTKLKIAFAADRHDTIGIDAVAMCVNDIVVQGAEPLFFLDYLACDKVVPEKIEAIVAGIAEGCHQAGCALIGGETAEMPGMYSAGEYDIAGFTVGVADKAKLVTGADIAPGDTVIGLASSGVHSNGFSLVRKLLLEEDGYGLNDVVPELGAPLVDVLLAPTKIYVKPLLGLLEQLPVKGMAHITGGGFIENIPRVLPEGVNVDINYGSWPVLPIFDLLQKKGGVSNRDMFTTFNMGVGLVLVVAEADGERALELLKAAGEEAYLIGRVTEGERIVTFTGAEV
>NZ_LN831776|879985:891647|881648_882539_+|WP_020430566.1|DBSCAN-SWA
MTYPAVSTAVDLVNAPLLYKGKVRELYDLGEEVLIVVTDRISAFDYVLDPAVPEKGNVLNRLSAFWFGQTSELMENHVVHIDVDRLGGIVKDREALRNRIMVVRKAERIDIECVVRGCITGGGWRQYQETGKVNGIGLPAGLRKNAQLSQPIFTPAAKNDVGHDEDIPFEKMQELIGAELALELKEKSLKLFAFAREYCEERGIILADCKFEFGLLDGKVILIDEIFTPDASRFWAKDKYALDIEIDSMDKEPVRTYLSASSWDKNSTPDPLPAEVVEETTRRYLDIYHRLTGKTL
>NZ_LN831776|879985:891647|883767_886014_+|WP_020430571.1|DBSCAN-SWA
MTQQVSAKEPTAEQIAEQKIYNQFGVSDSEYELITSFMGRKPNYTEIGVFSVMWSEHCAYKNSKPLLGRFPTSGPRVLMGPGEGAGIVDIGDNQAVVFKIESHNHPSAVEPYQGAATGVGGIIRDIFSMGARPVALMNSLRFGKLESDRVKYLFEHVVSGIAGYGNCIGIPTVGGEIMFDNSYDGNPLVNAMCVGLIDHDKIQRGVAKGVGNPVFYVGPPTGRDGIHGATFASVELSEESEAKKTAVQVGDPFMEKLVMESCLELIDSGIVLGIQDMGAAGLTCSSAEMASKAGNGLELYLDQVPQREDGMTPYEMMLSESQERMLFVVEPKDEAQAQEIFDRWGVICRKVGKVTDDGRLKLFHHGEVVGDMPVKALVDECPIYKKPSAVPAYYEENASVDTLRYAEVKDLGGALHTVLASPTVASKAWVYNQYDYMVRTSTAVRPGSDAAVVTIHGTRKGLAMTTDCNGRYVYLDPEVGGRIAVSEAARNIVCSGAKPLAITDNLNFGSPEKPEIFWQMERAVDGMAEACRVLDTPVIGGNVSLYNENASGAIYPTPVVGMVGLVEDTDHITTQAFKQEGDAILLLGVTKAELGGSEFQYAVHGLTEGRPPELDLATEQKLLDAVLAAIRSGLVRSAHDLSEGGLAAALAESCISGSIGANVEWSAGGLRRDVALFSESQSRIVLTAAPGRAEELRAAVAAYGVPAEIIGTVGGDRLRVSLDGEAVLDEAVAALKTTWEDAIPCLMK
>NZ_LN831776|879985:891647|889201_889819_+|WP_039790034.1|DBSCAN-SWA
MMQWSRIAVFASGQGSNFAALAEAERAGQLGGGRIELLVSDRPEAPVAKRAEEAGIPALMLRPKDFASRELYEAEIVAELQRRDIGLIVLAGYMRLITPVLLTPYAGRTVNIHPSLLPAFAGKDAIDQALDYGVKLTGVTVHFVDGGMDTGPVIAQRSVAVEPGDTVESLAERIHQVEYELYPEVVRALAEGKVELDGRKTVIRE
>NZ_LN831776|879985:891647|885998_887495_+|WP_046501155.1|DBSCAN-SWA
MSYEIKTGNKQENPILWTGDFYNEGTGSGDIFDTLKEECGVFGVFGHPEAASMSYYGLHALQHRGEESAGICVADGRDFHYHRGMGLVKEVFDKDKIASLVGNMSIGHVRYSTSGDSRLTNAQPLVFKYRDGDLAIATNGNIVNEPLIRKQLEQSGSIFQTTSDTEVLAHLIARSQKEFVEATKDALQQLVGGFAFLLMTNDKLIVASDTHGLRPLVMGRVGEAYVFASESCALEVIGAQFVRDIEPGELLVLDQNGFREDRFAEPQRKALCAMEYIYFARPDSDLNGSNLHAARKRMGSRMALEAFVDADIVTGVPDSSISAAIGYAEQTGIPYELGLIKNKYTGRTFIQPSQELREQGVKMKLSAVRRVVEGQRVVMIDDSIVRGTTSRRIVNLLREAGATEVHVRITSPPFKNPCFYGIDTPDRRELIASYKTVEEICHEINADSLAFLTPAGLIQAIGGYNSGDYKGGLCLSCFDNDYPTQVDFGGEEKDGCSC
>NZ_LN831776|879985:891647|890099_891647_+|WP_020430581.1|DBSCAN-SWA
MSIKRALVSVSDKQGIVDFCRGLSALGVEIISTGGTSTLLAKEGVPVIGISDVTGFPEIMDGRVKTLHPAVHSGLLAVRDNEEHTRQMQELGLDYIDLVVVNLYPFAETIAKADVSYEEAIENIDIGGPTMLRSAAKNHAFVSVVVDAADYATVLEEVRAGGDTTLETRKRLAAKVFRHTAAYDALISDYLANVTGEPLPERYTVTYEKIQDLRYGENPHQKAAFYRKPLAAQDTLTSAEQLHGKELSYNNINDANAALQIVKEFEEPAVVAVKHMNPCGVGVGASVYEAYQKAYNADPTSIFGGIVAANRIIDADTANMLKDIFLEIVLAPGFTEEALDILTKKKNIRLLKLGNLSTAAARKSSFVVTSIEGGMVVQESDVHSVNPEELQVVTNRKPTEEELKQLLFGWKVVKHVKSNAIVLAADDMTVGVGAGQMNRVGAAKIAIEQAGEKAKGSVLASDAFFPMGDTLEMAAKAGITAVIQPGGSIKDEESIKVANEYGIAMVFTGVRHFKH
>NZ_LN831776|879985:891647|879985_881281_+|WP_020430564.1|DBSCAN-SWA
MIERYSRPEMRAIWTEENKFNAWLEVELCACEAWAELGVIPHEDAAKLRKNAKFDIGRINEIELETRHDVIAFTRAVSESLGAERKWVHYGLTSTDVVDTALGYLLRQANEILEKDIINFIEILKDKALAYKDTPMMGRTHGVHAEPTTFGLKMALWYEEMKRNLERFRHAANGVQFGKISGAVGTYANIDPFVEEFVCRKLGTSPAPISTQTLQRDRHAEYMAALALVATSLDKFATEIRALQKSEIREVEEAFAKGQKGSSAMPHKRNPIGCENISGLSRVIRGHMMTAYENVPLWHERDISHSSVERIILPDATMLLNYMLNRFGNIVKNLTVFPDNMKRNMNRTFGVPFSGRILTKLIDKGFSREQAYDTVQPRAMQAWEEQTQFRDIVEATPEITAVLSPEEIEDAFNPSWHLKHVDTIFRKLELI
>NZ_LN831776|879985:891647|882849_883095_+|WP_019913657.1|DBSCAN-SWA
MLKATVYVTIKKSVLDPQGVAVQGALHSVGFQEVESLRIGKYMELTLDTDNRAEAEGRLKEMCEKLLANTVIEDYRYELED

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_020430564.1|879985_881281_+	adenylosuccinate lyase	A0A2H4UUU6	Bodo_saltans_virus	1.8e-23	28.1
WP_020430566.1|881648_882539_+	phosphoribosylaminoimidazolesuccinocarboxamide synthase	A0A0M4JBD3	Mollivirus	2.9e-41	34.9
WP_019913657.1|882849_883095_+	phosphoribosylformylglycinamidine synthase subunit PurS	A0A0E3FJ99	Synechococcus_phage	2.2e-07	36.7
WP_020430568.1|883100_883790_+	phosphoribosylformylglycinamidine synthase subunit PurQ	NA	NA	NA	NA
WP_020430571.1|883767_886014_+	phosphoribosylformylglycinamidine synthase subunit PurL	A6N228	Microbacterium_phage	4.7e-165	42.4
WP_046501155.1|885998_887495_+	amidophosphoribosyltransferase	A0A0M3SGR2	Mollivirus	5.7e-50	31.9
WP_020430577.1|888164_889205_+	phosphoribosylformylglycinamidine cyclo-ligase	Q58MH8	Prochlorococcus_phage	3.6e-67	44.7
WP_039790034.1|889201_889819_+	phosphoribosylglycinamide formyltransferase	M4QRX9	Synechococcus_phage	5.8e-25	37.1
WP_020430581.1|890099_891647_+	bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase	Q58MG4	Prochlorococcus_phage	5.9e-74	50.3

Sequences of DBSCAN-SWA_3

Nucleotide sequences of DBSCAN-SWA_3

>NZ_LN831776|2879522:2889953|DBSCAN-SWA
CATGAGACCGTTTCGCATTCGTCTTACATTCATACTAATGGCCCTGATTGGCATATCCATGATCGGCGCCGGGATCACCATGGCCAAGCTGTTTAAGGATTCGCATATTTCCGCGCTGGAAGAGAACATGTCCCGGGAAATAAATCTGCTCTCCGGCACCTTTCAGTTTACAGACACGGATAGTCCGGGCGCTGTCAGCTACTATACGGAGCAGGCAGAACACATAGCCAAGCTTACCAATTCACGGATTACTTTTATTACTAAGGACGGCAAGGTCATCGGTGACTCCGAGAAAAATCCGCTGGAGATGGACAACCATTCCACCCGCGAGGAGGAAGTGCTGGCGGCAAAAGAGGGGATCGGCCGTGCGATCCGGTACAGTGACACGCTTAACCGCGAGATGCTGTATGTAGCAGGTGCCGTTGTTTCCGACCAGGGCTTTGATGGTTATATCCGTCTGTCCATGGCCCTCGATGCGGTCACCGAAGGCTTGAACCGGGCCTGGATGGTCATGGCGGGCGGACTGGTGCTGCTGTTCATTGCAGCAACCTTTGTAAGCTACAAGGTTGCCTCCGGCATGACCTCTCCGCTTGAGCAGATTACAAGGGTAGCCCGGAGGATTACAGATCTGGATTATGATGCCAGAGTTCCAATGAACCGCCGGGACGAAATCGGTCAGCTTGCAACTGCAATTAATGCCATGGCCGACAGTCTGCAAGCCCAGCTCAAAACGATACGTGACAACGAAGACCTCCTGCAGAGCGTGCTGGATAATATGACAGGCGGCATTGTGATGATTAACGCAGAAGGTGAGATTGCGCTGTTGAACCGGGCGGCGGAGCAGCTGCTGGATGTGAAGAACAGCGAGATGGCCGGCCATTCCTTCAAGGAGCTGAAGCATCACTATGAGCTGAGCCGTTTGATTGAGGAAGGGGTCTCCCGCAATGAGGCGGTTCATGAAGAGCGCAGTATCTATAATCCTACCGAACGGATCGTGCGGCTCGACGGTGTACCGATGATTCAGGACGGCTCCAACCGGGGTATGCTGTTTCTGCTGCAGGAGGTGACGGAAATCCGCCGTCTGGAAAAAATGCGCAGCGAGTTTGTAGCCAACGTCTCCCATGAGCTGAAGACACCGGTCGCTGCCGTCAAGGGCTTTGCGGAGACGCTGCTTGGGGGCGGGGTCAAGGATGAGAAGACCGCGCGCTCTTTTCTGCAGATTATTTATGATGAGAATGAGCGGCTGAACCGGCTGATTGGTGACATTCTGGAGTTATCCAAAATAGAGTCCAAACGCGCGCAGCTTGAATGCTCACCTGTGCATCTGATAGAGTTCTTCGATTCCCTGCTGGAAACGCTCAGCAAGGTGGCTGAGAAGAAAAATATCAGCCTGAACGCATCAGTTCCCGAAGAACTGTTCATGGAAGGGGATGAGGACAAGCTGCGCCAGATCTTCATCAATCTGATCTCCAATGCCATCAATTACACCCAGGATGGCGGAAGTGTAAATGTCAATGTGGTGAACGGCCAGAAGGCTGATGGTACGGAGACAGTCGTTTTTACCGTCAGAGATACCGGCATGGGGATTCCGCGCAAGGACCTGCCGCGCATATTTGAGAGATTCTACCGGGTGGACAAAGCCAGATCGAGAAGCTCCGGCGGAACCGGGCTTGGACTGTCGATCGTCAAGCATTTGGTGGAGCTGCATCATGGCTCGATTTCAGTAGAAAGCGACCTGGGTATCGGCAGTTCCTTTATTCTGGAGCTTCCTCTTCTGCAGGATGAACCACACTGAGGTTACCGGATTTATATGAATAGTTCAGGGCAATCTTTCCCTTTAGACGGATTGCCAGCTAAGGCCTGAAGCGCTAGTATTAATTTGAACAAAAAAATAGGAATAGTTGGCAAGGTACGCTTAATACAGATGCCGAAGCCGATGCTGGAGCTGTTGTGAATCTCATTCATATTGGCTAGAACCTGCATTCTATTGCACTTTCAATCTATATAAGATTCATGCTCAATCTATACAGGATTAGTGTGGAAAACCGGAAATATCATGAAACCTTTGTTATTTTACACCGGGTTAACATTCCGGTGATATGATGGGCTTGCCTGCAGTTTTGTAAAATTGAAAACATAGAAGACGGGGGAAACTATGGCACAACGATTGCTTGTCATTGAAGACGAACCAACACTGTCCCGGCTGCTGTCGTATAACTTGACGCAGGAAGGCTATGAAGTCACAGTGGAGGATCATGGAACGGCAGGGTATGACCGTGCGGCTAGAGAACCTTTTGACTTGATCGTACTGGATTTGATGCTGCCGGGGATGAACGGGATTGATATTCTGGATAAGCTGCGCAGCCAGGGCATCCGCACGCCTGTAATTGTGCTGACGGCCAAAAATGCCGAAGAGGATGTGGTCAGAGGGCTGAAATCAGGGGCCGATGACTACATAACCAAGCCCTTTGGCGTATCGGAGCTGCTTGCCCGTGTCAGTGCGGTGCTGCGGCGGATCTCCGGCCTCGCCGAAGAAGTTCAGCCGGAAGCTGCAGTATCCGCTTCAACCATTATCCTGGGACAGCTGGAGATCTATCCCGAGCGGTATGAGGTTTCGCTGGGCGGACAGAGCATCAATCTGCGGCCCAAGGAGTTTGAGGTTCTGCTGTATCTGGCCCGCAAGCCGGGGGTGGTGCTGACGCGTGATGACCTGATGAATGCTGTCTGGGGCTTCGACTATATCGGCGGGCAGCGTACAGTGGATGTGCATGTCAGCTCCCTGCGCAAAAAGCTGGAGCTCGACCCGGAATCGGTGCATATCGATTCCATTCGCGGCGTAGGCTATAAACTCGTAGTGAACAAAAAAAGAACGCCAGTCATTTAAGATGACGGCGTTTTTTTCGTAAACCTGACATGTGATTTTACACAGCGTTAACAATTCTCTTCAACTGCATTTACACTGAAAGCTTATCATGGGGTACGAAGATGATGAGAAGGAGACGCAAAAACTAATGAAATCCATCATTGACATAGAGAAGCTAGATCTCTACTATGAGTCATTTCACGCGCTGAAAAGCGTGGACCTGCAAGTGCCGGAGAAACAGGTGACTGCTTTTATCGGACCCTCCGGCTGCGGAAAGTCCACTTTGCTGCGCACACTTAACCGGATGAACGACATGATCCCGGGTACACGGATTGAAGGCAAGGTCAACATTGGCGGCAAAAATATTTACAGCGATGAGGTAGAAGTGGAAAGCTTGCGCAAGCAAGTGGGCATGGTGTTTCAGCAGCCGAATCCATTCCCCAAATCGATCTATGACAATGTGGCTTACGGGCCCCGCCTGCACGGAATCCGCGGCAAAGCCGAACTGGATGTGCTGGTAGAACAAAGCCTGCGCCAATCCGCCCTGTGGGAGGAAGTCAAGGATTTTCTGAAGAAATCCGCACTCAGCCTGTCAGGCGGCCAGCAGCAGCGTCTTTGTATTGCCCGTGCGCTTGCGGTTCAGCCGGATATTCTGCTGATGGACGAAGCGACTTCTGCGCTAGACCCGGTTTCCACACTCAAAATCGAGGAATTGGTGCAGGAATTACGGGACAAGTATACGATTGTTATGGTCACACATAATATGCATCAGGCCGCACGGGTATCGGGCCGCACAGTATTTTTCCTGAACGGTGTGATCGTGGAGGCTGCGGATACTGAGATGCTGTTCTCGAATCCCAAGGACTCCCGCACCGAGGACTATATATCAGGACGCTTCGGTTGATCGGGGAGCAGTATGCTCCTGGGAATGACAAGCTGACCATATGTTTTTGAGGAGGAACGCTTTTATCATGATTCGCAGAAAAGAATTCGATAAAGATTTGGAAGAGCTGCGCAGCCTGCTGCAGCAGATGGGCGAGCATGTGACAGATGCGCTGGAAGGCGCGATACTGGCTCTGCAGACCCTGGATACTGCCCGTGCACAGGAGATTGTGAAAGCGGATTTGCGGCTGAATGCCATGGAAGACAGAATCATGGAAATCGGCTCGCGGCTTATTATCACCCAGCAGCCGGTAGCGAAGGACCTGCGCCGCATTATTGTTGCCTTCAAAATATCCAGCGATCTGGAGCGTATGGGTGATCTGGCGCTTGATGTGGCGAAGGTCACTATGCGCGTTCAGGGTCAGCAGCTCATTAAACCGCTTGTGGATATTCCGCGGATGGCAGAAGTGGTAACCGGAATGATAACGGAAGCGATCCAGTCCTATCTGGACGAGAATACCGATCTGGCCTACAAAATGGCTCAGGACGACGACCAGGTCGATCATTTGTATAGCGGCATGATCAATGAGCTGTATGCGTTTATGGTTGAAAAACCGGAGTGCCTGAATCAGGCCATGCTGCTGACGCTGGTCGGCCGTTATATCGAGCGGATAGCCGATCATGCCACCAACATTGGTGAGAGTGTAGTCTACCTGGTAACCGGCAAACGTCCTGATCTGAATCAATAGAGGCGCTTTAGCCCGGTTTCCACGGAATTGTTCAATCAGAACGGGTTGGATATTGCTTTGTTCAATGCAGAAGGCAAGCTTTCTTTAATGGGAGCTTGTTTTTTTGTGGAAAAATACTGTTACCGGTTCTATAGCGGGAAGCGGATGGATATCCTGCAAGCAAACAAAATGCCGGGCAATTACGGCTTAGACGTTTTTGCTTGAGCGGGGCATATGTTAAAATGTAAGGAGTATGCAATGTAAAGGCGAGGTGCTAAAGTGGACAAGTTGATTCTTATAGATGGCAATAACATTATTTACCGCGCATTTTTTGCAATGCCGCCGCTGACGAATACCGCAGGGCAGCAGACGAACGCAGTGTATGGATTTACGACTATGCTGCTGCGTTTAATTGAAGAGCATAAGCCCACCCATATGATTGTTGCGTTTGATGCGGGGAAGATTACGTTCCGGCATGAAGGTTATGAAGATTATAAAGGCGGCCGCCAAAAGACACCGCCTGAGCTCTCCGAGCAATTCCCGATGCTGAAGGACCTGCTGCGGAATCTGGGTGTGCCGCAGTTTGAGATTGACGGCTACGAAGCCGATGATATCATCGGCAGCATCTCCCGCGAGGCGGACGAAGCCGGACGGCAGGTCATGATCGTGTCCGGGGACAAGGATATGCTGCAGCTGGCTTCAGAGCATACAACGGTGGCTTTGGTGCGCAAAGGGGTTACCGAAGTCGAAATGTACGGGCCCCGGCAGATCCGCGAGAAGTATGATCTGACACCGCAGCAGATCATTGATTTGAAAGGTCTGATGGGCGATGCCAGCGACAATATTCCCGGAGTGCCGGGCGTTGGTGAGAAAACAGCGCTGAAGCTGCTGCAGCAGTTCGGGTCTGTGGAGGGCGTGCTGGCCGGAACGGACGAACTGAAGGGCAAGATGAAGGAGAAGCTGGAGGAGCATGCCGACAGTGCCATCATGAGCAAGAAGCTGGCAACGATTTACCGTGAGGTCCCGCTGGAACACGCCTGGGAGGATATGGTCTTCACCGGAATCCGCAGCGATACCGCCGGCCCGGCGCTGGCCAAGCTGGAATTCAAATCCCTGCTGGAACGCCTGTCGCTGAGCGCGTATGCTCCTGCAGGCGGGAACAGCGAAGAGGGCGCCGAAGCCGTAGAGGCTGCTGTGCTGGACATCACCATTGTCCACGAAGCTGAGCTGCCGGACCTGATTGCCGCTTTGCCGGGCATTTCTGCGCTGCATGTCGAGTCTAACGGCGAGAATCCGCACCGTGCCGAAGTGATCGGCTTAGGCCTGTCCTCCCCGGAGCAGCACTACTTTGTGCCGTTTGAGCTGCTTAAGAGTCCTGCAGCGGAGAAGCTGCGGGATTGGCTGGAAGATGAGAAGGCGCCGAAGAGCGGGTACGATCTGCACCGTGCAGATCTGGCGCTGCACTGGCAGGGGATTGCTTTTGCCGGAGCGGCTAATGATGTTCAACTGGCTGCTTACCTGCTGGACCCGACGGAAGCCAACCAGAATCTGTACGACCTTACAGCCAAATATGGCCTGCCCCGCTTGTCTCCGGATGAAGAGGTGTTCGGCAAAGGCGCCAAATATAAAATACCTGAGCTTGAAATTCTGGGCAATCATATCGCCCGCAAAAGCGCCGCCGTGCTTGGCATCGTACAGAAGCAGCAGCAGGAATTGACAGACACGGACATGACCGGCCTGTTCGTTGATCTGGAAATGCCGCTGTCGCGCATTCTGGCCGATATGGAGAAGCAGGGAATTGCCGTGAATAAAGAGGATTTGATCGACCTCGGCAAGGAATTTGAAGCGCAGATTTCCAGGCTCGCCGCGGATATTTATGCGATTTGCGGCACCGAGTTCAACCTGAACTCTCCGAAGCAGCTGGGGGAAATCCTGTTCGTGAAGCTGGGCCTTCCAGTGGTCAAGAAGACCAAAACAGGTTATTCCACAGATGCCGAGGTGCTGGAGAAGCTGGCTCCTTACCATGATGCGGTCAGATTGATTCTGCAATACCGTACCATTGCCAAGCTTCAGTCGACCTATGTGGAAGGCCTGCTCAAGGAAATTTCCCCCGATACCGGGAAAGTGCATACGTTCTACCGCCAGACCATTGCGGCAACCGGACGTCTCAGCAGCCAGTTTCCGAATTTGCAGAATATTCCGATCCGGCTGGAGGAAGGCCGCAAAATCCGCAAAATTTTTGTACCCTCCGAGCCGGGCTGGTCGATTCTGGCGGCGGATTATTCGCAGATCGAACTGCGGGTGCTGGCGCATATTTCCGGTGACGAGCGGATGAAGGAAGCTTTCGTGGAAGATATGGATATTCACACCAAGACAGCGATGGATGTATTCGGGGTCAGCGCCGATCAGGTGGACAGCAACATGCGCCGTTCCGCCAAAGCGGTCAACTTCGGGATTGTGTACGGCATCAGTGATTACGGGCTGTCGCAGAACCTGAATATTTCGCGCAAGGAAGCTTCGCAGTTCATTGAGCAGTACTTCGAAGTGTTCAAGGGAGTGCGCCGCTATATGGATGAGATTGTGGTGGAGGCACGCAAGCAAGGTTATGTCACTACACTGCTGGAACGCCGCCGGTATTTGCCGGAGATCAATGCGAAGAACTTCAATTTGCGCTCTTTTGCCGAGCGTACAGCCATGAATACCCCGATCCAGGGAACGGCAGCGGATATTATTAAGCTGGCTATGGTCCACATGGACAAGGCGCTGCATGAACGCGGACTGAGAAGCCGGATGCTGCTGCAGGTGCACGATGAGCTGGTATTCGAGGTGCCGGAAGATGAGCTGGAACTGATGAAAACGCTGCTGCCTGAAGTGATGGCAGGTGCTTTGAAGCTCTCTGTGCCGCTTAAGGCGGAGGTAAGTTATGGAAGCAACTGGTATGAAGCGAAATAGGCTCCCCGCAAGGGGAGGATATCCGGTATAATGGAGAAGAGGTGAGCCATAATGCCGGAATTACCGGAAGTAGAAACTGTCAAAAGAACACTTAATGCCTTAATTACAGGCAAGCAGATACAGAACGTCACCGTCCGGCTGCCGCGGATCATTCAGCGACCGGATGATATTCAGGCTTTTGCCAACATGCTGGCAGGCCATACAGTAGTACAAGTGGAACGAAGAGGAAAGTTTTTACGTTTTGTGCTGGATGGCCTGGTGATGGTGTCCCATCTGCGGATGGAGGGCCGTTACGGACTTTACCGGGGAGAGGAACCGCTGGACAAGCATACCCATGTCATCTTTCATTTTACCGACGGCACGGAGCTGCGGTACACGGATGTGCGCCAGTTCGGCACCATGCATCTGTTCCAGCCGGGAGAGGACCTGCTGCTGCCGCCGCTGAAGAAGCTGGGGGAGGAGCCGCTGGCACCTTCTTTTACACCGGAACGGTTCAAGGAAATTGTCTCGGGAAAAAGCACCAAAATCAAACCGTTGCTGCTCAATCAGGAATATGTCGTCGGCATCGGCAATATTTATGTAGATGAAGCGCTGCACCGTGCCCGCATTCATCCGGAGACAGGTGCCAAAGCGCTTACAAGCAGTCAGCTGGATCTCTTGCATCATGCAATTGTTGCAACCTTGACAGAGGCTGTAAATGCAGGAGGCTCCTCCGTAAAATCGTATGTCAACGGCCAGGGAGAGAGCGGAAGCTACCAGCATCAGCTGCTTATTTACGGACGCAAGGACCAGCCTTGTGCGAGCTGTGGAACACTGATCGAGAAGACCGTGGTGGGAGGCAGAGGCACGCATTATTGTCCAAGCTGCCAGCCGCAAGCCGGGATCAGCAAGTAAACGTTGCATCGTAAGATTTGGCACTGCCGGACTGTCGGAATTACGTTAAAGTTGTCCATGCAGCTATAAAAGTCAGGCACTCATTGCCCGTCCCGCCCATATACTGTGTGAAGAATGCTGATTAGAGCGAACGGAGCCCTGCCCTGGAGCCATCCAGGAGGGCTGCCGGTTCTTCACGGGAGGGATTGCGGGTGCTCAGCCCATTTTTTTCACTGCTGCTGCTGGCGTTTGCCCTGAGTTTGGACGGTTTTGGTGTTGGTATTACATATGGGCTGCGAAAAATGAAAATTCCGCTGCTCTCGATCCTGATTATCTCGCTGTGCTCGGGGATCGTTATTTATGTCTCTATGCAGGTCGGTGTGCTGCTGGCCAAGGTGGTTTCTCCGCATGCCGCTTCCAGTATTGGAGCGGTTATTCTCGTCTTGATGGGCTGCTGGTCCTTATTCCAGATGCTTACGCAGAAGGAGAAAGACCATGACGGTAAAAGCCCCGGAGATCAGCACGGGCGTGCTGACCACGATGCCCGGCTGGAGACTGCTGCCGCTTTTGCCGGAGGTGCTGCGGCGGCTGAAATTCCCCAGGCGGAAGAGGGGGAATCTCCAAAATCAGCGGTGTTCTCGCTGGAGCTGCGGCATTTGGGCGTAGTCATCCAGATTCTCCGTACCCCGTCTTCCGCCGATATGGACGCCTCCGGCAGCATCTCCTCGACGGAGGCGATGGTGCTCGGGATTGCACTGTCGCTGGATGCATTCGGCGCGGGACTTGGAGCAGCCCTGCTCGGGTTCGGTCCGGTGTCTACATCGCTGATGATTGCCCTTTTCAGCGGCACCTTTTTGCTGCTGGGAATGAAGACGGGATTGAAGCTGTCAGGAAGCTACTGGATGAAACATGCTGCTGCACTGCCTGCGTTATTATTAATTGCAATGGGAATAATGAAGCTATTATGAGGTGAGTACATGATTATGGGCTTAACCGGAGGCATTGCCTCCGGAAAAAGCACCGTATCCGCAATGTTTGTGGATAAGGGAGCGCGGCTGGTGGATGCGGATGTCATTGCCAGAGAAGTAATGCTCCCCGGTCACCCGGTGCTGGCCGCTGCTGTGCAGCAGTTCGGGGAAGACATCCTGCTGCCGGATGGCACACTGAACCGGGCCAGGCTTGGAGAGATCGTTTTTAATGATTCTGAAGCCCGGCAGAAGCTGAATGATCTGACCCATCCGGCGATTCGCCGGGAAATCAAGAACCGTATGTATGCCTTGGAGCAGGAAGACCCGCAGCGTTTGACCCTTGTAGATATTCCACTGCTGTATGAGTCCGAACTGGACAATCTGTTTGAGGAGATCACCGTAGTCTATGTTCCCCGTGAGCTGCAGCTGGCCCGCCTGATGGAACGAAACGGACTGACGCTCCAACAGGCTGAAGGCAGACTGCAGGCCCAGATGGATATTGAATTGAAGCGCAGCAGGGCCAACTATGTCATTGACAACAGCCGTGATCTGGCTTATGCGAAGCAGCAGGTTGATGTGCTGTGGGACAGGCTGGGTCTGTTATGAAATGGCTGCGTAAAAAACGGGTGCTGCTCCTGCTGTTTATAGGCTTTACAGCCATTTTATTTTTAAGTACGAACTGGATGTCCTGGTTTTATCCCATTTACTATAAAAATGAAATCCGCACACACAGCAACACCTATGAGATTGACCCGTTCCTTGTTGCGGCGATCATCCGGGTGGAGACGAACTTCAAAACCGGCCGTGAATCCAAAAAGGGAGCAATCGGCCTGATGCAGCTGATGCCGGATACCGCCAAATGGGCGCTTGAAAAGGCCAAGCTGCCGGATGTCTCCCTGGAGCGGCTAAAAGAAGAGCCTTCGGCCAATATTGAGCTGGGTACCTGGTATCTGTCTTCCCTGTCCCGGAAGTTCGAGGGCAACCGCATAGCAGTTATAGCTGCTTACAACGCGGGCCCGGGGAAGGTGCAGCGCTGGCTGGATGAAGGTGACTGGGACGGCACTGAGGCTGCGGTGAAGAATATCCCGATTGGCGAGACTCGTCACTATGTGCAGCGTGTGATTTATTATTACGACCAGTATACGGAAATCTATAATGAGTTTTAA

Protein sequences of DBSCAN-SWA_3

>NZ_LN831776|2879522:2889953|2884273_2886946_+|WP_020427948.1|DBSCAN-SWA
MDKLILIDGNNIIYRAFFAMPPLTNTAGQQTNAVYGFTTMLLRLIEEHKPTHMIVAFDAGKITFRHEGYEDYKGGRQKTPPELSEQFPMLKDLLRNLGVPQFEIDGYEADDIIGSISREADEAGRQVMIVSGDKDMLQLASEHTTVALVRKGVTEVEMYGPRQIREKYDLTPQQIIDLKGLMGDASDNIPGVPGVGEKTALKLLQQFGSVEGVLAGTDELKGKMKEKLEEHADSAIMSKKLATIYREVPLEHAWEDMVFTGIRSDTAGPALAKLEFKSLLERLSLSAYAPAGGNSEEGAEAVEAAVLDITIVHEAELPDLIAALPGISALHVESNGENPHRAEVIGLGLSSPEQHYFVPFELLKSPAAEKLRDWLEDEKAPKSGYDLHRADLALHWQGIAFAGAANDVQLAAYLLDPTEANQNLYDLTAKYGLPRLSPDEEVFGKGAKYKIPELEILGNHIARKSAAVLGIVQKQQQELTDTDMTGLFVDLEMPLSRILADMEKQGIAVNKEDLIDLGKEFEAQISRLAADIYAICGTEFNLNSPKQLGEILFVKLGLPVVKKTKTGYSTDAEVLEKLAPYHDAVRLILQYRTIAKLQSTYVEGLLKEISPDTGKVHTFYRQTIAATGRLSSQFPNLQNIPIRLEEGRKIRKIFVPSEPGWSILAADYSQIELRVLAHISGDERMKEAFVEDMDIHTKTAMDVFGVSADQVDSNMRRSAKAVNFGIVYGISDYGLSQNLNISRKEASQFIEQYFEVFKGVRRYMDEIVVEARKQGYVTTLLERRRYLPEINAKNFNLRSFAERTAMNTPIQGTAADIIKLAMVHMDKALHERGLRSRMLLQVHDELVFEVPEDELELMKTLLPEVMAGALKLSVPLKAEVSYGSNWYEAK
>NZ_LN831776|2879522:2889953|2881676_2882405_+|WP_020427952.1|DBSCAN-SWA
MAQRLLVIEDEPTLSRLLSYNLTQEGYEVTVEDHGTAGYDRAAREPFDLIVLDLMLPGMNGIDILDKLRSQGIRTPVIVLTAKNAEEDVVRGLKSGADDYITKPFGVSELLARVSAVLRRISGLAEEVQPEAAVSASTIILGQLEIYPERYEVSLGGQSINLRPKEFEVLLYLARKPGVVLTRDDLMNAVWGFDYIGGQRTVDVHVSSLRKKLELDPESVHIDSIRGVGYKLVVNKKRTPVI
>NZ_LN831776|2879522:2889953|2889389_2889953_+|WP_020427944.1|DBSCAN-SWA
MKWLRKKRVLLLLFIGFTAILFLSTNWMSWFYPIYYKNEIRTHSNTYEIDPFLVAAIIRVETNFKTGRESKKGAIGLMQLMPDTAKWALEKAKLPDVSLERLKEEPSANIELGTWYLSSLSRKFEGNRIAVIAAYNAGPGKVQRWLDEGDWDGTEAAVKNIPIGETRHYVQRVIYYYDQYTEIYNEF
>NZ_LN831776|2879522:2889953|2883355_2884015_+|WP_020427950.1|DBSCAN-SWA
MIRRKEFDKDLEELRSLLQQMGEHVTDALEGAILALQTLDTARAQEIVKADLRLNAMEDRIMEIGSRLIITQQPVAKDLRRIIVAFKISSDLERMGDLALDVAKVTMRVQGQQLIKPLVDIPRMAEVVTGMITEAIQSYLDENTDLAYKMAQDDDQVDHLYSGMINELYAFMVEKPECLNQAMLLTLVGRYIERIADHATNIGESVVYLVTGKRPDLNQ
>NZ_LN831776|2879522:2889953|2888796_2889393_+|WP_020427945.1|DBSCAN-SWA
MIMGLTGGIASGKSTVSAMFVDKGARLVDADVIAREVMLPGHPVLAAAVQQFGEDILLPDGTLNRARLGEIVFNDSEARQKLNDLTHPAIRREIKNRMYALEQEDPQRLTLVDIPLLYESELDNLFEEITVVYVPRELQLARLMERNGLTLQQAEGRLQAQMDIELKRSRANYVIDNSRDLAYAKQQVDVLWDRLGLL
>NZ_LN831776|2879522:2889953|2886997_2887840_+|WP_020427947.1|DBSCAN-SWA
MPELPEVETVKRTLNALITGKQIQNVTVRLPRIIQRPDDIQAFANMLAGHTVVQVERRGKFLRFVLDGLVMVSHLRMEGRYGLYRGEEPLDKHTHVIFHFTDGTELRYTDVRQFGTMHLFQPGEDLLLPPLKKLGEEPLAPSFTPERFKEIVSGKSTKIKPLLLNQEYVVGIGNIYVDEALHRARIHPETGAKALTSSQLDLLHHAIVATLTEAVNAGGSSVKSYVNGQGESGSYQHQLLIYGRKDQPCASCGTLIEKTVVGGRGTHYCPSCQPQAGISK
>NZ_LN831776|2879522:2889953|2879522_2881316_+|WP_039787644.1|DBSCAN-SWA
MRPFRIRLTFILMALIGISMIGAGITMAKLFKDSHISALEENMSREINLLSGTFQFTDTDSPGAVSYYTEQAEHIAKLTNSRITFITKDGKVIGDSEKNPLEMDNHSTREEEVLAAKEGIGRAIRYSDTLNREMLYVAGAVVSDQGFDGYIRLSMALDAVTEGLNRAWMVMAGGLVLLFIAATFVSYKVASGMTSPLEQITRVARRITDLDYDARVPMNRRDEIGQLATAINAMADSLQAQLKTIRDNEDLLQSVLDNMTGGIVMINAEGEIALLNRAAEQLLDVKNSEMAGHSFKELKHHYELSRLIEEGVSRNEAVHEERSIYNPTERIVRLDGVPMIQDGSNRGMLFLLQEVTEIRRLEKMRSEFVANVSHELKTPVAAVKGFAETLLGGGVKDEKTARSFLQIIYDENERLNRLIGDILELSKIESKRAQLECSPVHLIEFFDSLLETLSKVAEKKNISLNASVPEELFMEGDEDKLRQIFINLISNAINYTQDGGSVNVNVVNGQKADGTETVVFTVRDTGMGIPRKDLPRIFERFYRVDKARSRSSGGTGLGLSIVKHLVELHHGSISVESDLGIGSSFILELPLLQDEPH
>NZ_LN831776|2879522:2889953|2888031_2888787_+|WP_020427946.1|DBSCAN-SWA
MLSPFFSLLLLAFALSLDGFGVGITYGLRKMKIPLLSILIISLCSGIVIYVSMQVGVLLAKVVSPHAASSIGAVILVLMGCWSLFQMLTQKEKDHDGKSPGDQHGRADHDARLETAAAFAGGAAAAEIPQAEEGESPKSAVFSLELRHLGVVIQILRTPSSADMDASGSISSTEAMVLGIALSLDAFGAGLGAALLGFGPVSTSLMIALFSGTFLLLGMKTGLKLSGSYWMKHAAALPALLLIAMGIMKLL
>NZ_LN831776|2879522:2889953|2882532_2883288_+|WP_020427951.1|DBSCAN-SWA
MKSIIDIEKLDLYYESFHALKSVDLQVPEKQVTAFIGPSGCGKSTLLRTLNRMNDMIPGTRIEGKVNIGGKNIYSDEVEVESLRKQVGMVFQQPNPFPKSIYDNVAYGPRLHGIRGKAELDVLVEQSLRQSALWEEVKDFLKKSALSLSGGQQQRLCIARALAVQPDILLMDEATSALDPVSTLKIEELVQELRDKYTIVMVTHNMHQAARVSGRTVFFLNGVIVEAADTEMLFSNPKDSRTEDYISGRFG

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_039787644.1|2879522_2881316_+	HAMP domain-containing protein	W8CYF6	Bacillus_phage	6.0e-38	33.7
WP_020427952.1|2881676_2882405_+	response regulator transcription factor	W8CYM9	Bacillus_phage	2.3e-36	35.2
WP_020427951.1|2882532_2883288_+	phosphate ABC transporter ATP-binding protein	W8CYL7	Bacillus_phage	3.9e-15	32.4
WP_020427950.1|2883355_2884015_+	phosphate signaling complex protein PhoU	NA	NA	NA	NA
WP_020427948.1|2884273_2886946_+	DNA polymerase I	A0A1B1IST8	uncultured_Mediterranean_phage	2.6e-45	31.9
WP_020427947.1|2886997_2887840_+	DNA-formamidopyrimidine glycosylase	A0A127AWE5	Bacillus_phage	1.6e-20	29.7
WP_020427946.1|2888031_2888787_+	hypothetical protein	NA	NA	NA	NA
WP_020427945.1|2888796_2889393_+	dephospho-CoA kinase	NA	NA	NA	NA
WP_020427944.1|2889389_2889953_+	lytic transglycosylase domain-containing protein	K4NWI2	Pseudomonas_phage	5.3e-17	43.1

Sequences of DBSCAN-SWA_4

Nucleotide sequences of DBSCAN-SWA_4

>NZ_LN831776|4939412:4961489|DBSCAN-SWA
GTTATGCGCCTGCGAGGGCTTTTACCTGAACCTGAAGTTCATTAACCTGCTTCCGCATATCCTGGGCTTCCTTCTGCTGCTTCTGCACAACAGTAGTCAGCACAGCGATGATATCCATCAGAACAACGGACTTGTGATCCGTGGTCGAGAAGATTTGCGGAACGTCCTCGGCGATGAAGCCGATATTCTGTTTCTTGGCATTTTCCGCTTTGTAGTTAAAGGTAACAGGCTTCAGTTTGTTCAGCAGCTCCAGGGCTTTTTTCACCGGAAGGCTGGCGATGTTCTCCTTGAAGGTTCTGGAAGAGGTCTGGGCGAAATTGGTCGCCCGCAGGTTGCCGTTCACATCCAGCTTGTAATCGTCGGTTGGGGTTTTGCCGATCCCTACATTGCTGCTGGAGTCCACGGTCACCGCGCCCGCTACCTGAATCAGCTCATCATAAACGTGATCCTTGCAGACTAAGGTCTGCAAATTGTCTTCGATTCCGGCTTGCCATACATTGTTAGCTGTGTCCCAGGCGATCCGGGCCTTTTTGTCCGTTCCGCGGCCGACTTCAATGCCTTGGCTAACCGCCAGACTGCCGCTGATGACAGCGTCCTTGGCGGTCAGTTTATTGCTAACCGCAGCGTCTTTCGCTGTCAGCGTGGCGGACACTGTTGCATTTGGAACCGTCAATGTTCCACTTAGCGACACATCCTTCACGGTCAGCACTCCGGTTAGTGCTGCGTCCTTTGCTGTCAATGTGCCGCTGACTGCGGCGTCGGCCACCGTCAGCTTCCCGGATACTGCCGCATTGCCGTTCACATCGAGCTTGGCAGCGGGTGTGGCGGTGCCAATCCCGAGATTACCGGAAGCGATCTTCAGCACTGCGCTCAGGTCTGTAAGCTCCTGGTGCGTATGGCCGCTGTAGGCAAGCTGCTTCAGGCTGCCTGCTACGCCAACCTGCCACTCATCCAGCGCTTCGTTCCACAGAATTTGTGCTTTCGGATCGGTTCCCCGCTCCACGGCAATGCCCTGGCTGAGTGTAAGACTGCCGCTGACGGTTGCGTCTTTGGCGGTTAAAGTACCGCTGATGGCTGTGTCAACAACGGTCATTTTACCTGAGACTACCGCATTGCCGTTCACATCCAGCTTGGCGGTTGGCGCTACGGTGCCAATCCCGAGATTCCCGGAGGCTATCTTCAGCACACCGGTCAGAGCCGTCAGCTCCGGATGGGTGTGGCCGCTGTACGAAAGCTGCTTCATACTTCCGGCTACCCCAGCCTGCCAGGCATCTGTGGATTCGTCCCAGAGAAGCTGCGCTTTCGGGTCGGCTCCCCTGTCCACGGCAATGCCCTGGCCGAGGGTAAGGCTGCCGCTGATGGCTGCATCCTTCGCGGTCAATACACCGCTGACCGTTGCATCCTTCGCCGTCAATGCACCGCTGACCGTTGCATCCTTGGCCGTTAATGTCCCGCTGGCAGCGGCGTCTACGGCGGTCAGCTTGCCGGAAACGGCCACATTGCCGTTGACATCCAGCTTGGCGGCCGGCGCTGGGGTGCCGATCCCGACATTTCCGGAAACTACGGTAAATGCGCCGGACAATTCGGCGAACTCCGGATGGGTATGGCCTTTGAACTCAATAGCCTTCAGTGCGTTCGGGACACCGGCCTGCCATTCATCGGCAGTTTCATCCCAGATCAGTTGGGCCGGGAGCGCGGTCCCGCCGCGGAATACCTCCAGTCCCGCATTTTTGACAACCGGCGTTGCTTGGGGTGCATACTTGTTCACTCTAATAATGTTGTCTTCAACTTCCAGGGTAGCTGCATTGATCATCACTGTATCGCCGTTCACAGTCAGATTGCCAGTTACGGTCAGATCCTTGGAGATAACGGCATTAACCGCTGTGAGGGTTCCCGCAACCGCTGTGTCGCCCTGCACATCGAGCTTTGATTTCGGATCATAGGTCCCGATACCGACATTTCCTGCTCCGGTTACGCTGAAAGCCGTGAGCCCCCCCTTAATCTTGACATCCATAAGTGCCAGCGGGGTATTGGTTCCGATCCCTACTCTGCCTTCCGAATCCGCGAACAGGGCAATGGTATCACCAAGCGCGTTGTAGAGCTTGTTCTGGCCGCCTTTGCCCGTGCCGAATTCCGAGAGCGTAACTCCGTCGCCATAGAACCAGGCCTTCTGCACGTTGTTCCAGACGATCCGCGCATTCGGCAGTTCCTTGCCGCTGCTGTCCAGCCCGCGCGGGGCCTCGAAGCCGCCTGCGACAACATTGCCGGCCACGACTGCATTTTTGCTTACCGCAAGATCTGCCGCATGAATCGCCTTGTTAAATGCAGCATCTCCTTCGAATGTCGCTTCGCCATGGGCAGTGACCTTGCCCGAAAACGTTGCTGCTCCGGCGATTTCCGCCTCTGTCCGGAAAACAGCCTTGCCGGCCACATCCAGAACTTCAGTAGGATTATCTGTGCCCACACCCACTTTGCCGCTGCGGGTCAGGCTGAGTACAGTTTTGCCTGCGGTCCCCAGCTTCCAGCGGTCCTTCGCCCATTTGATCTGTGCACTCGTCTCCGTTCCCTGGAGTACTTCAAGACCATCACCAACGGTCACCGTTCCGGCAATAGCTGCACTGGCAGCGGTCACCGCACCAAGGACACTGGCGTTGGCAGCCTTCAGTCCACCGGGTACATTGACATTACCTGATGTATCTACAACCATTGCGGCGGGTTCTGTAGGCGTTGCAAGCTGCCACTCATCCTTAGTCTCGTCCCAGGTAATCTTGGCAGCAGGCTGGTTGGGTCCCCGGTAGATTTCCAATCCGCCGCCCGAAAGTGAAGAGACCTCACCGCCATCCTTATTGATCGTGACCCATGGACTGCCGATGTCCAGCTCGTCCGTAGTGATGCTGGCAGAAGTCCCCCGGACTTCCAGATCTCCGGCCACTGTAAGATTGCTGCCGACGGTCAGATCATGATGGACATCTACATCCCCCTCGGCACTGGCGCTTAGTGCCAGTATATCGGTCTGCGGATTGTAGATCTGACTGTGGGTGTGCAGGGAATCCGCACTCGCCATTTGCGTCAGCTTGTCCCAGGAGCTGCCGCTTGCGATATTTTCCAGAGCGCTGCCTGTGCCAACCTTCCATTTGCGTTCACTCTCGTTCCAGATAATTCTGGCGGCAGGCTGCGATTCCCCCCGGTAGACCTCAATCCCGCTCTCATTCGCGGGCGGCGTCCCGCCTTTGAACTTGTTAATCTCGATCACATTATTGGTAACGACCAGGTCTTCACGCTCAACAGTAGTCGTGGTACCTTTGACAATCAGGTTGCCGTCGACCTTAAGCTGACCTTGCACCGCCAGCCCGCCGCTGATATCCGCACCGTTGTCGACCGTAAGTGTTCCCTGTACCTCCGCGCTGTTCGTAATCTCAATATCGCCCTTGGCAGTTGCCTGGATTACAGTGTTGCCCTTGCTGTCACTTAGAGAATTATGCCGGTGCAGGCCATCCGCATCCGAGCTCACGCCTCCGGTCAGCGCATCCCAATTGCTGCCGTACGCAATATTGGACAGCTCATCTCCCAGCCCCAGCTTCCATCTGCCGTCCGTTTCGCTCCAGACCAGCCTGGCGCTCGGTTTCTGCTTCCCCCGGTAGACGTCAATGCTGCTCTGGTTCAAGATGGAGCCGTTGCTTTCGGATTTGTTCAGCTCAATCCGGTTGCTGGCGACAACCAGATCTACTTTGTCCACATAGGTGGTCTTGCCCTTTACCGTCAGGTTGCCCTCGATGGTAGCAGAGCCGCCCACATTCAGATCAGCCTTGAGCTCAGAATTGCCCTGGCCCTTCAGGGTTCCGCCAATCTCCAGACTCCCGGAAGCAGACACCTTCCCATGTTCATCGGCGGAGAGGATCGTTCCCCCTGACGGTGTGCTGAGCGCACTGTGCTTGTGGGCCGCATCGGCCAGTGAGCCGTTCGTCAGCGAATCCCATTTGGTTCCATACGGAATGTCGGACATGCTGCCTTCGAGTCCGATTTTCCACTTGCGCTCCGCCTCATTCCATTCCATACGGGCTTTTGGATTCTTTATGCCCCGGTATACGTCCAGGCCCCCCTTGCTGCCAAGCACTGCATCATTGTCTGCCTTGTTCACGGTCAGGAAACTGTCCGCCACCTCCTGCTCCACTTTCTTGACGACTACCTCTTCTTCCCTGACAATCAGCTTGTTGACCGTAAGCGTCTCGCCGACCATCAGTTCATGCGGAATATTTACATTTCCGTCAGCACCAATTTCCAGGGCCAGCAGGCTTTTATCCTCATTATGGAATTGTCTGTGGGTATGCAGGGCATCCGCGTTGCCGGTTCCGCCGGTCAGCTCTTCCCACTGCTTCCCGTCCGGGATATCCGTCATGTCTCCGTTTGCCGTGCCGATCTGCCAGGACTTCGCCGTCTCGTTCCAGGCAATCTTGGCATTAGGCAGTGTCTCTCCCCGGAAGACCTCCAGCCCGTCCTGCTTGGACACCAGGCTCCCTGACACGGTCAGTGTCTGGTCGATCTGGATGTTGCCCTGCGCATCGGTGCGGAGAGCCGGCTTCCCGTCCGCCGAATGCAGCTGACTGTGGGAATGCAGGCCATCGGCAAGCGAGCCGCCATGCAGCTGCTCCCACTCTGCTCCATAGGCGACATGGAACATGCCGCTGGCCGCGTCCCCCTCCTTCACATCGGTTCCAATCATCCACCCTTTGCTCTTTTCATCCCACAGCAGCTTGGCGCTGGGCTCGTCCTTGCGGATGACTTCAAAGCCGCTATTGTTCTCCTTACTGGCATTTTTGTTGAGCGTAACCATATTTCCGCCCACCATGACCTGAGGCACATCCAGTACAGCCATGCCTCCGCTGACTTCAATCCCGCTTTTGGCAGAGAAAGATCCGGCTACGGCAACGGAACCCGACATATCCACGTCCCCGGAATCATTAACCTTGAACACCTGTTCACTGCCGGCAGTGACAGCAAGCTCGCCGTTTACATCCAAGGCTCCGTAGGAGCTGATCGCACCGGTTCTCAGATTGCCCGTAAATTCAGTCAAGGCTGCGTGAACATTGAGCTTGTTTCCCTCTTTTCCATCCTCTTTAACGGAGTTGCTCAAAAAGGGCTGGTCCGGATCTTCCTTGGATCCGACAATAATTTTGTCAGCCTTAAGCGTTTCTCCGCCTATGGCTCTGGTTACAAGTTGCGTTCCGTCCACGTCAGTATCATAAATCTGGTCGATGCTAAGCGCTCCGTCCTGATTATGCTTCAGGGTTACACGGCCTAACAGGATGTCCTTGCGCACATCCTTAGGCTTCAGGGAGCTGGCCTTGATATCCGCTTTTTCCCACACATGAATATTTTCCCCGCCCCCCTTGAGCAGGTCGGGGTCTGCCAGCTCTTCCATGTAGCTGACTGAAATATAGATCTGATCCGAGGTGCTGTATCCGGACAGATCCAGCACCCGCTTCGGATGGGTGTCACTGACCAGAATTTCCTGGCTGATCTCTTCATTGTTGTCCGGGTCCGTGATCCGGTTCAGGGCAAACCCCGGATCAATCTCTACTTGGGTCAGCTCTTTTGGATTGACCTTAAGCCCGGTGACGACACCCCAATTATGGAAATAACGGTTATGCAGCCCGCGTGCGCGCTTATGATAATTCTGATCCAGTGTTAAGTCCTCTTCCTTAAGCAGCAGCCCGTTGAAATAATTCATGCGTTTCATATCCTTTGGCACAATCCCACTCCTCCCGGCTTTCATAGTTACAGCTTATTCAGTCTTGAACGGACTCCTCTTCGCCGGCAGACAATTCCTCCAGCACCTGGATGGCCCCGCTGATCCGTGTCATGGCATACCCCAGATTGCTGCGTTTCTCATCCAGCTCCTGCATCATTTGCCGGCCGGATTCGAGTTCTGCCTTCAGTTCATTCATGCGCGCTTCCAGTTGTTCCTTCATCATTTCATCCTCCAATTTTTAGGCACCCTGCAGGGTTGCGATTTGTTTTTGCATTCTGGTTATAGCCTTCTGCTGGTCTTTCACCACACTGGTCAGAACGGCGATGATATCCATCCCGCTGATGGCCCGCTGGTCAGGGTCGGCCAGAACCGCCGGCACCTCTTCAGCGATAAAACCAAGCGTTTTTTCCTTCGTACTTCCTTTGTATTTAAAAGAAACCGGGTTCAGCCCGTCGAGCAGCTGCTTCGCTTCTTTGACGGGAATATCGGCGATGTTGTCCTTCAGCTCGCGTGAGGACCACCAGTACATGCTGCCGTTGGCATAGACACCGCCGCTGGCATGAAGATAAATGCGGTCCCCGGCATCATTGGATACACCGATATCCAGCACGCAGTTTTCCCCGCTGGTCGGGTAGAACTTGATCCAAGCCGAGTCGCCGCTGCCGCCGCCGGGATCGGAAGGGAAGATAATCCCGTTATTGCCGCTGCCCGCACTGGGGATCAGGGCATTTTTCACTTCAAGGCTGCTGTGAACCGAGGCGTACGACCAATCATTGCCGTAATTGAGCACCAGGTGGTTTCCATTATCGACCAGGGCTCTGCCGGGAGCTCCACGGCGTCCGGAATAGCCGATGTAGAAGTCGGCACAGCGTACATACGCCGCAAAATTATCTGCTACATCCAGCTTTTTAAATCTTCCGTCAAAGTTGAACACATCGGTCTTGATGCTTCCTGTGATCTGCAGATCCCCTGCAATGCGGGCGCTTCCGTTCACCTGCAGGAATCCGTTCACATCCAGCTGATCCCAGACCGCAACCTTCCGTTTGCCGTCCGGGGAGGACGAGTTGCCGATCAGCATCAAGGATTTGTAAGTGGTGGTATCATTGCTGATCTCCGCCTGATTATGAGCCTGATCCGGGAATCCCGACCAGGCCGAGGTGAAGCGGATCGGATTCTTGCCGCTCAGGACTCGCAGCTCCCCGGCCACATCCAGCTTATCTGCCGGGGTCAGCGTTCCGACGCCTACATTGCCGGAGGCATTCAGCGAGATGTGGTCATTGGCATCATTAGAGGTGCCGATCTCCAGCGTGCAATCCTCGCCGCTGCGGGGATAATATTTGATCCACGCCAGGTCTGATCCGCCGCCGCCCGGGTTCGCCGGGAAGATGATGCCGTTGTGCTCGCCTTTGCCTGCACTTGGAATGATTTCCTGGGCAGCCTGCATAACACCGTTCACGTACAGAAATCCGTTCACATCGAGGCGGTCCCAGATCGCAACCTTTCTTCCCTGTCCGGCTGACTGGTTGCCTACAATCATCAGTGCTTTGTGATTGGTGATATCATTGCTGATCTCTGCGCCGTTAATCTGATTGTCCGGAAATCCCGACCACACAGAGGTGAAGCGGACAGGATTCCTGCCGCTGAGGATACGCAGGCTGCCGTCGATGTCCAGGGAATCCTCCAGCGCCTTCCGGGGGCCGATTCCGACATAGCCGGCCTTGTTCCAGGAGAGGACCGGCCGGTCGGTCCGGGACCCGTCGCTGTTGGCCGTTCTAGTGCCCAGAACCCCGCCGCTGTTCCCGAATAATACAGGCCCGTCCACTTCAGATGCGGCAAAAGGCTTGCCGGCTCCGAACCAGCCGAGACCATGCGAGCTGTCAATCGTGTCCGGGTTCGTCCCCTTAAGCCAGAAGGTTGTCCCGTCCTTGAGCGCCAGATCCGCATCGCTGAACAGCTTGCCGGAGCTGTTGAAGCCAAACGACGATCCGCCCGATGATGACAGCTTGCTGTGTCTGTGCAGCAGGTCGGCGAACTCATATTTGATCAGGCTGTCCCACTCGTTGCCGTAGGCAATTTTTTTGAGATCGGTGCCAAGTCCGGCCTTGAAGCATTGATCGGCCTCCACCCATACAATCCGGGCATCATGGATGCCTCCGTCGCCCCGGTAGACCTCAAGCCCGCCATCCCGCGGTCCCGGAAACTCATAATCCGGATCATCCGTGTTGGGACTGTTGACCTCTACGAAGCTGTTCATAATCCGCATTTCACTTTGCGATTTATCCTTGCTCTGCAGAATAAGCTCACCCTGGAGCGTTAAATCTCCGGCGATGTTAAGCGCCCCGGTAAAACGCGTCTCCGGTGCGCTGACCTCCAGCACCTTTCCTTCCTGGAGCGTATATACCGCAGGCATGCCAGCCAGCGTCGCTTCATTCAGCTCCATATTGTCGATGCTGTCTTCGCTCTTTGCTTTGATAATCAGCTTCTCTGTAACCATCTTTTTGCCCGCTGCACCTGCGTAGGTCCGGAGCGGCGTACGGGCAACGTCACTGTCGTAGTCGAAAATACATGCGCTGTCGATAACGATTCCATTGCTTTCCTTGCGCGGGACAATCCGGGCCAGAACGATATGCTCAGAGCTGTCAGGCTTCTTGGTACCGTGGCTGATCCGCCCCCGCTCCCAGATGTGAATCTTCTCTCCCTGGCCCCGCTCAATATTGCGGTCAGTCTCCATCTCTTCATAACTGACCCAAATATAGATGGTCTCGTTGGCGTTATATTCGGACAGATCCACCGGATTGTCAGGATGTCCCTCATAGATGAGGATTTCCTGGCTGATGCTCTCTTTCTTCTTCGTCGCAGCATCTTCAATCACTACCTGATTCAAAGCCAGCCCTTCGGCTACCTTTACCTTCATGTATTCACCCGGATCCAGCACAGGGAGCACCTTCAGCCCGCAGACAATGCCCCAGGTATGCAGGTAACGGTTATGCAGCCGCTGCAAACGCAGGTAGAAATTCTGGTCCAGCTTGTAATCCTCCGCATTCAGGAAGAGCCCGTCAAAGTAACGCATTCTTGCAAATTCTTTTCCCATGATTTACTTGCCTCCGTTCTCTATCTTCTAATTCTCTGTCATACCCCCGAGCAAGGTCTCCATTCCAACACGCCCGTACACCCCCAGGCACATTTTCGGAACTTCAATATTCAAGCTGGAATTGGTGTAAAAAGGTTTTTCCTTACGGATCACCTCTTGCAGAATTTGCACTTTGTTCTGCAGGATGCTCCGGCTGTACGCGGGAAGGATGACATGAACGGAGAAATAGCTCGGCTCCGCCGCCCCCACCATGGTATTGATTCCTACACGCTGCCCGATGCCGCAGCGGACAGGCTCTTCGTAATCATTGATCTGAATGGCGGCCTCTTCCCCTGCATAGACCTGCAAATATTCCGCCAGCCCGTCCAGCGTTCCGCGTTTTTTGTAGAGCCGGACAATGCTGCTGATCAGATTGCGGTTGACGGTGCTGCGGGCCGCAGGAAGCGGGAGAATCTGCATAGGGGCAAGCGCACGGTCCCGGTTATCCTGTTCCCCGTCATATTCGAGGCCTTCTTCCAGCTCCAGGCCTACCCAGCCTGCGAGCCAGGGCAGAAACTGGGAGGGGGCCCTGCCGGGATCAAAATACTGATGCAGTCCATCCAGCAGTGCTTCAATCCCGACCGACTCTTCCCCGGCCGCTCCTGTTTTACCGGAGAGCATGGCTTCAAAGGCCTTCAGGAACCGGCCCAGAAAAAATTGTTCGTCCGATTCCCCTGCTTTCTGCTGAAATACTCTGGGAAGGTACTGCACATAGCTATAATCGTTCTGGCTGCTCACGATTCCACCTCAACTTTCAGGTCCTTCAGTTTAAATAACTGGAACGGCAGCAGGTCGGGGGAATCCAGCGCCACACTCGTAACATGATCGATCCCGGATATGCCTTCTACGAGATGGTACAGATCAGAGGCATACAGCTTTCTGCCCGGAAGCCAGCCCAGGCCTTCCTCTCCCCCGCTTACCGGATCTAGGAAACGTGTAATACTGTCGATAACCGTGCTGCCGATACTTTTGTCCTTGGCGGACACTGTCATCTCGATCACAATATCCCGGTAATCGGGCTCGACCACATGGACACGCGTGGTCAGCAGCTTGCGGGCGTCCAGATAAGCTTTGACGCTCTGCTTGATCTGTGTCATTTCTCGCAGCAGATCCTTCTGATTATCCGTCTGGAGAATCAATACCACAGAGACATGCCCGAAAGCTTCTTTGTTCACTCCGGTGCCGTTCTCCATATCTGTATTGATCAGACAGAGAGTGCGCACCGCAAGATCGGGATAGGTGTCCAGAATGCCCGGAATATCCAGCAGGCTCTGCTTGGCCAACAGCTGAAAATCCGCTGCCGTTACGGCTCTGTAGCACTCCGAAAACTGCTTCACCCCGCGCCGTATCCCGCTTGTCAGCTCCTCCCCTTCTGCCAGGGCAACACCCAGCAGCTTGAGAAACTGCAGTTGGCTCTCTTCCGTCACCTGGTCAATCCGGTAGAGAACCATTTCGCTGAACCATGCAAACAGCTCAATCAGTGTGATGCCGGGGTCGGAGGGATTATAATTCGTCCAATCCGGATCGTAGAGCGGGATCAGCGTTTTGGCATCCGCCACTAGCTCATCAAAGCCAAGATCGTCCAGGTTGGGTACTGGAAGCGGCATGGGTTCTTCCTCCTTTGTTGTATAAGCTTTAAGCTCAACCTATACAGGTCATTTTCTTATGGCTGCTCCTCCGGAAAACAATAGCGGCACCGTGCCGCTGTCCCTGGCGCCTCCTTAAGGCCGGTCAGAAACTTCCGCTCCTCCTTAAGGATGGCTCCAAGCCTGCAGTCTTCCGTGGTTCCGGTCAAATCATGCAGCAGGCCTGTGTTCTTATCCAGAAGATACGGGAAGATGTGCTCTTCCGGTTTGTTGATCAGATGCGTCCCGCCATAGATCAGCTCATCCTCTTCAAGGAAAATGTTATCAGAGTGGATGCTGCGAATCTTGAGGGGGGTGGTGTTGACATACTCATCAGTCTTGCTTAAGAAGACAATATCCTTCGGCTCAAAGACGGCGATTTTCACAAAAAACGATTCAGCACCTGAAGCCAGCCCGTTAAGTATATAGGTGCGGACTGTTAAGTCATCGGTGATGTCGAATTCAAGGTCGCTGCCTTCAGGATAGCTGTGCTCCAGCGGTTGCCCGTCCAGAGTCTGACATTCCAGGATGTCCCCGTCGATCGATACGACGATCAGCTCAACCGGCTCATAAGTTCTGTAGCGGAGCCTGATCTTTCCATTCTCCTTGAACCCCTTAAGCACCAGCGATTTCACTTCGCTTCCGGCCTCTACCCGCTCGGCAAGCGCAAATTGAATAGAGTTGTCGTCAGAACGGACCGCACTGTACTTCGGGTAAGCAGCCAGAGGTTTATAAGGCCCGTTCTCCAGGGGTTCAAGACTTGCCGTAAAGCACTGCACCGAAGCCTTGATGGCAATGCCGGATACATAGTCCACACCCGGTGTATTTTTGATCACAGCATAGACCTCGGAAACATACAGGTTCTGTCCCAGCTCCCAGCCCGCAGCCCTGTCTCCGCCATAGAGGGGATGAAAAAACTGCTTCAGGTTGTCAATAATCCGTCCCTCCTCCACCTTCCGCTGTTCTACGGAGGTAAATGCTACAGCGGCCTCCACTCCGATCCGCACGTAATCCGGGCCAATCACTTCAATTCCCGGGTCGCTCGTGTCCAATGCCGCAGAGGTCCGTTCGCACAGATAGGCTTCAATTTCACTGAGCAATTCCTGGCTGGGGACCGGCTTTGGCTCATCCGTTTCCGGCACCACAATGATTGTGGCTGTGCCCGGAACGAATTCCAGATCACGGTTCATGGCGCTAAGGCATTTCACCTTGGCAATCTGGGGCATCGCCTCACGCACCAGCCATTCTATGTCCTCGGCGGTAACGCCTCTGTCCCAGCTTTTCAGCGTATGCGGCCCGCGGATTTGAGCCTGCTCCGCCGCCTCCTGGTCAAAGCCGCCGTCCGCCGCCACCGGATTAGTCACCGAATCCAGCCAGCTGAAGCTGTCCCATATCTTGGTGACCGCTCCTGCGGCAACATTGCCGGCTGCTCCGCCGCCATACTTATAGTCGCACTCAATGTTGTCGGTTCCGGTCGGCGGGATCATGCCGTTTCTTCCGTCCCCGAAGATGATCGTCCCGCTGCTTCTGTCCAGCATATAGTGCCTTCCGTCCGAGGCAGACAAGGAAAAAGTGTCAACTTCCTCCCACGGCACCCACTCGCCTTGCCCCGGCGCCTCCCGGACCCGAAGTCGCTGTCCGGGCAGCACAGGCGTCTTGGATAACTGGAAGCTCTGGTTCTCTTCGCCGTTGCTGGAGCCGGGGATCTCACCGGCAACCGAATTGGAGTTGCGGGCCCATACCGCATTCGCAAAGATAGCATCGACCTGGGGAAAGATCTCAAAACGTCCCTCATCCAGCCGGGCGCGGATCCAATACTGCTCTGTTCCGAACAGCGGGCGTTTAGCGATATCCGTTGGAACGGCAAACTGCAGAATCTCCCTCCGGGTGAAGCCCCTGATCTCGTCATTTACACTTAGCGTCAGCCATCTTCTGCCGTCCCAATACTCCCAAGCCACAACCGGACGCCTCAGCTGTTCCCCGTTTAACGGAAAAAAGAGCGATACCGGCAGGTTGCTGATGTCACGGTCAAAGCCCAGATAGAACGTAGGCTCAAGCTCTGCACAAGGGTAAAAGGGTTTGAAATATTCCCCTTCCGCCAGGCAGGCAGCCGTTTTGTCCGCAAAGCTGAAATTGTTCTCCGTGAGCACCGTTTGCGGGTGCCCCTCCAGCGTATGGCTGTAAGCAATGCTGAGCCTGCGGATGGAAGGGGGAGCATAGGTTGCTTGTGTAACCTTCAGCTGGGCTACCTTGATGCTTCCCTCCCCAAGCTTGACCTCTTCATCCTGGTATTCATATTTCGCTTCCTCACCATAATTCCCGCCGGTGATGCGGGCACGGATCCAGTAGCGCTCTTCCCCGTTCAGCGTCAGCGGCTTGATCCCCGGACACTGGAAGCTGAGCATTCCACTTCCGGTAAGGCAGGCGCTGCTGCGCGTACTGCCGCCTGCAGCCGCAGCTTCTCCGTCCAGCGTCTCTTCCAGGCTGCCGATACCGAGCCATTCCTTGCCGTTCCAGTACTCCCAGCCGAGTCTCACATAAGGGGTATCCGGCAGCTTGCTGATTTCCGGATCAGACAGCTCAATCTTCAGCGTTATCCGGGAGCCCGGTTTGGAGAAGGCCTCGCTGCACGCGATATAGAAGGTGTCGTTCACTTTGGGCTTGTCTCCAAAAGGATAATAATCTTTGCCCATATCCAGCGAAGTGCCGTTGTTGACCGCCATATCCGGCATCAGCGGCACCGGGCTCACCAGCTTTAGCTCCAAGCGGATATCTTCGATATCCGGCATCAGATCAGCGGCGGTTATGGGTGTCTTCAGCTCGGCAAATATCCACTTATTGGACCATTCCCGCAAACGCTCCGCTTGCTCGTAACCGGCAATTGTCTTCGCATGAACCCCGGACAGGTGATCAAACTGAACCACCGCCCTCCAGGCAGAATCCTCCTTAATCCCGGTCATTGACGGCGACAGCTGTACGGTATTCCCCTCTTCATCGAAGCAGAACCAGTCCATATCGGGCAGACTCCCGGCCCCTCCTGGCGCATCCGCAGCCAGAGCCAGGGCTGCTTCCGGCTTGTTGAAGTAAACCGACAAGCGGCTGCCCGCTTCTTCGAACCCGAGAAGCTCCGAATGGCCCAGGTACAGCCTGTGGACCACCGTCGAATCGCCTTTGAACAACTTGGCCCTTTGTCCGGAAGGCTCCTCAGCAAAAAGATAATCCTGATTGCTCCACTGGTCTTCTTCGGGATCAAGGCTTACGGCCCTGACCAGCCGGGGCTGGATGACCGTCAAATCCTTTTCGGTTTCAAAAATCACCTCTGCCTGATTCTCGGGCTGGGCGGATACCCGCGTCCCTGCCGGAATCGTGCTGCTGGTGTCCGCATCAGGCTTCTGCTTAAAGAGCAGCGGTACTTTGGCTGATCTGGGCGGAGTCGGATGAATACCGATCAGATTCAGAAAGGATATGAAATTTTTCTCGGGCGCCTGGTTCAGCCGGCCGATGACTTTGCCCATCATTTGGGTAAAAATATGGACCAGCGCATCCACCTTCTTGTCTGCTTCCAGCTCCGTCAGATCCGTCCATTCCCTGCTGCAGTATTGGTAGATTAAGCGTCTTAGCTCCGGAACCAGCTGTTCCTGATTCCGCTTGTCAATGGTAGGCACTTTGTTTGGCATTATTTCCCCACGCTTTCAAGGAAGAATGGATAGACCAGATTATATTTGCTGTTGCTGGCCCTGATTGAATAGTCAATGGACACCTCCAGCTGAGACTGGTCGGAGCGCGGCGTGACGGTAATATCGTCCACTTCGATCCGCGGCTCCCAGTTCTGCAGCGCTTCTTCAATAAAGCTTCTCAGCAGCGTAGCGGTGCTCATCGTATTAGGCGCGAACACCAGCTCGTTCAGCCTGCAGCCGAAATCCGGGCGCATGACCCGTTCGCCGCGGGCGGTTGAAAGAATCAGAAGGATAGATTCGCGGATGGAATCTTCTCCATCTGAAGAATTGATGCTCCCTCTTTGGACAGCGAAGGGATATTTCCAGCCCCGTCCCAAAAAATCTACAACTTCCATAATTCAGCCTCCTATTAAGACCGTTCCTGCCGCAACCACCTTGCCTACCGGCAGATCGGCCGGATCATTGCATGTCAGCGCCGGATCGCTGTGTCTGGCGGCCATTTTTCCGTTGATTTTTACGCTAGCGCTTCCGGCGATGATTTTCCCCTGATTGGTTGGAGGCTTTTGAAAAGGGCCTCCCTGCGGAACATGTGCCGGTGTATTCGTGGCCGTGGAATCCACTGTAGCTGCCGGCTGCCCCATAATCTTGACATTTGCGCTAAGCGCGCCGTCCAGAATGCCCGTAAAAGGATGGGGCAACGGCGTCGGAACGGGCGCCGGACCGGCAGGAAGCATCACGATATGCGTATCGGTAGCCAGAATGCGGTCGCCCTTTTTCGCGGCAGGCTGTCCCATGTATGAAGCTCCTCTCTAATTAATATTGACCGTAGCCCCTTTGATCGTCATGCTGGCCGCTGCTTTGACCTCCATCCCCGCCGACGCTTCAATCCTGGTGTCCGCCGATGATTTCATTTCAATCGTTTTCGCGGAGAGAGACAGCTTCCCGCCGGGGGCGGATATTTCGATGTCCTGTCCGGACAGGACCGACAGCTTATTCGCTTTGGAATCGATGACGATTTTGTTCTTCCCCGATTTATCCATGATCTGGATTTGCTCGGCGCCGCTTTTGTCATCCAGCCGGATTACATGACCTTTGGCGGAAGTAAGCGTAATGTTCTCTTTCCCCTCGGTATCGGCAAACTGCAGAATGTGTCCGCTGCGGGATTTGAACATACGGATATTGTTTTTGCCGTCTTTGTTGGTTTCCGGCGGTGTATCCTTTCCGTTCCACAAGGACCCGATCACATAGGGGCGGTTGACATCTCCATTCTCAAAAACCACCAGCACCTCATCATCCACCTCAGGCAGGCAAAAAGCCCCCCGCTCCTTCCCGGCCATCCATGAAGCCATCCGGGCCCAGTTGGATTCCGGCATGCCCATCAGCGGGATCTTTACCTTTACCCGGCCGGGTCCGGGTTTATCCGCATGGTTCGCGGAGTCATTGTTAATGACAATTCCCACCATCACTCCGAAGATGCGTCCCTCGTTAATCATGCTGTCGGCAAAATTGGTAATTCCAGGTCCCTCATTCATAGGCCAGTCCTCTTTACCCTAAAAGTCGTTGTATAACCCTTGCTGTCAATCTTGTGAACCGTGGATACAATATAATAGATGCCGCTGAAGCGCTCGCCCAGGCCGAGCAGCTTCACCGTTTGGCCTGCCCGGAGCTGCGGATTTCCCCAGCACATGCCCTCACCGGCGATGAAGTCGCGCAGGCGGCTGTTGTAGGCGGCGGAAGCCAATGTTTTGGCCTCGCTCATATCGAGCAGATGCTCCGCCATGATGGCGACCGGCGATTCCTCAATAGCTTTGGCGCTTAAAGAAAAGCCGGATTCTGTCCCGCCCATCTTGGTCGTCTCGTCTCCGGTCTTCGCTTCGGCTTCCAGCTCCTTCTTCTCCTTCACGTCCCAGCCCTTTACCTTCACCTTGCTCCCCCGGGTAAGCGCCCGCAGCTCCAGATTCAGCCGTTCAAAATCCTTCTTGAAGCTCAGCTCCGGCAGACCGGGGGCTTTCACCGACCTTGACTTGACGAAATACAGCTTCTTGTCATCCGCATAGAGCTCATAATCGAGCATGGCCGCCCGTTCCACCAGAAACTCGTAATTGCTCTGATTATTCTGGAATATGTAGGGATACACGGTTCCAGTATCGTCTACCACAGGGGTCAGTCCATGCTCTTTGGCGATCTCCGAAGCGATGTCGCTGTCCTTTTTCTTCAGAAAAGCTTTGCTTCTCGTCCCCATGCGAAGCCTGTGCAGCAGGTCGTACCCGCGAATGTCCAGCACGGAATGCTCCCCAAAATTCAGATCAAGCGCGGTAATCTCCCCGCTGATCATCGGCTGGAGCTTGTCGAGTCCAAGTGAAAGCTTCACCTTGTCTCCCGGCTTGATGCTCTTGAGATCGGTTCCCCGCCACATGCCGCTCCCGGAATTGACCATATTCATCTGAATGGAAAATAAAGCCGGCAGATTAATCTCATCTTCCAGCGTAACTCCCTCCACCGCCGCAGCCAGTTCTGCGGACAGCTTGCTTCCATTCAGCTCAATCTTATAATTCGCTACACTGGTGCCCATGCAATCCCCGCCTTAATCCGGGATGACCAAGGTCCTCCCGATATCGTTTTTTCCAGGAAAGCCGATTGGATTGACAATCTTGTTCAGCTCGGCAATCCTGCGCCACGCCAGCGGCTCCTTCAGCGCTTCATTGGCGATCAGATCCAGCCGGTCCCCGCTTTTGACCACCCACAGCTTCCGGCAGGCATTCAGACCCCGGTTGTCTTCGACGGTTTTGTCCGACTCTTCTGTGATAAAGGTAACATCGAGCAGAGAGCGGACCGGTGTGCCGTTCTCCATGAACATCGTGAACTTCTGCTCGATCTTGCTGAGAAGGCCGCGGTAGGTGAACCCGCCCCAGACAAACAGGCACACCGGCGGCTTTTTCGTATTTTTCCCGCTTACTTTGGGGTCAAGCAGCGAGGTTAGCAGCTTGGTTTTCTTGCGCACATCCGTGCGCTTCTCATAAGTGTCATAGAATAAAGAAACCTTGAGTTCAGGGGTTTCCGTGATTTGAAATTGCTTGTTGTTCTTCTCCCCGGTATACTTCCCTTCGAAGGAAACGGTGTACTCATTGGGGTTGAACATCACCTCAATGGCTCCAACGGGCATATCCAGAGGAATAATCTTCGCTTTCTCCGCCATTATCTAAGCCCCCTCCGATCCTTGCGGATCGCCATTTTCTTTTCGAGCACCTGATAGACCCGTTCAGCCAGCTGATTCAGCTCCGCAGTATCCATTTTTGCAGCAGGGGCCGCTGCCTTGGGGAAAGACTGGGAAGTAGGCGGGGCAGCCCGTTCCTGAGGAACCGGCTCCGGCCACTGCTGAACCGGCTCCGGCCGGGCAGCCTTGGGTGCTGCAGGTTTCCGCAGAATAAGGCTGCTGTATCTGCCTGCGGGCTGAAGGTATTCTTCTTGCTCAGGCCCGGCTGTGATGAGCCTGCCTCCGGGACCTCTTCCCTTCAGAGCCAAAGGCACCGCTTGCCCCTTGGCTGTGTGGATCAAGCCATTCTGTGGTGCAACTGAAAGTAAGCCCCCTATATGCGCTGGCCGCACAGCGCTGCTTAACCGGGCGGAAGAATGCCGCTGAACCATTGACCGGGGTTCTGACGGAACCGCAAGAAGCTGAAGGGGTAAGACGTCCGGCTGCTGCAGCCCGTCATGCACTGCCGCAGGTCCAGCGGGCAGCGGGTTCAGACGCTCAGACCGGCCCTCCAGCTTGTCCAGCGCAGCCGCCAGTCTCTGTCCTAAGCCCAGGTGAAGATTGGGGCTTACCAAGGACCGGGGGCCTGGACTTGGCCTGACGGATGGAGTGCTATGCTGTGCTTCCACCGTTGTCCCGGCTGAGCCTGAGCCTGCCCCAGGATGGCTCAGCGCCATTCTTGGCGGCTCAGCCTGGTCATGCCGGACCGCCGCTGGTTCAAGCTTCTGCCTCAAAGGCTGCTCGTTGTTTACAGTGTCAACGCTTTGATGCAGGATATAGGTCCGCAGCGTCTGCAGCTGACCATGAGCTGCGGGCAAATGCTGAGGTCCCCTGCCCGCAAGGGATTGCCCCTGCCGGGAGTCTCCGGAATAAGGCTCAAGTCTGCTTCCAATGCGCCGCCCTGCCAGATCCGTTCCGGCCGGAGCCGCTGCCGGCATTGGCAGAAGGTAAGACAACGGCGTGCCATCTGTCCGCTCCTGATTCCTCATGGCAACCTGAACGGTTACGGGCTCCACTGCACTTCCGGCAGGATCAAGAGTGCGATATCCCCTTGTTACAGGGCGTTCCGCGTGTTGCTGCTTCCACACTCTCTCCTGTAATCCATGGATGAGGTTCTGGTGTCCCGGAGAAGAGGCCGGACTGCCGATTCCCGCTCCACCGCTGCCTTGAGTGGTGTACAGCACTCGGTTTACTGTCCCCGGACCCGTCATAACCTGCGTTATGGGAGGATAAATGGAATGATGAATATGCATTTCCTTAACAGGATGAATGTTATTAATAACCGTCTCAGCAGGCTTGACTGCTTCCGGCTCCGCGAACAGCAAAGGATATTGCCGCAGGATCAGGCTCTGAAACCGGCTCCGCCATCGGGTTATGCCGTACTTCCCCAGAATGGCCTGGATGAAATCCATTTGCTTGTGGTTAGCAGGGGAAGCCGTTCTCCGAATGCTCCGGATCATTACCGGTACCTGTACAGCCCGTTATGGGTCAGAACCAGACTCTCCACCGCCACCGCACTGCTGCTGGCACTGAATGCCGGTCCTTCCCACTTGATGGGACAAGCCTCGATAAAGTTCCACCACACCTTTGGCGTGCCGGAATGATCCAGCAGACAGATGGACCCGCTGCGCCGTTTGACCACTCCATTAACCACATTTTGATACCAGTTCCACAGATATTCGTCGTTGGTAACCCCGTTTTTCAGCGTCAGATCTGAGTATTTGGTCTGTCCGAGGAAAACAAATTCCTTATGATTCTCACCGCCGAATGTTTTGCGTTCCACCTGGGTCTCAATACTAAGGCCGGAAACCTCGGAGAACCCGGCGACGGAGATCCCGTCGATCTCCACAATGAAGTTAAAGGCAAGATAGGGATCTTCCCTGTAACCGGGCACCCAATTGCTTTTCGCGCCGATATTTAAAATATTTGCCTTCATGTTATCCTCCTAAGCCTCAAAGAAGTTCTTCTTCTCTTCCCCGCCACCCAGCTTTTGGTTGATTTTGCTGACTTCACTGCACCAGCGGTTCCGTTCAGGATGCTCCAGGTTCAGCACAGCCGCATAGTCCCAATGCAGATAGTAGGTTAGAAAGGCTACCTCCTCGTAGAGGCGGTCAAGGGGGTAGCCGACTATTCCCCCGGCGATTCCAGTTCAAGCTCAAACGGCTGCTCGCATTTGGGGCATTTTGTATGAACCGTATTGGAGCCGTTCTGGTTAATCCGGTTATACATATCCTGCAAATAAGCAAAATCCGAAGTGTACAGCTCTTCAATTACTCTCGGCGTGATCATGCTGAGCCCGCCCAGGCTGGTTACCACTCTGGAGAGCAGAATCACCGTCAGATAAGCCGGGTTCTGCTGGACCCGGGAATCCCGGAGCGGTGTAATTTCATCCGCAGCAGTTGCCAGACGCATGGTGCCCTGCTTATGCAGCGTGCCTGCTTCATCCACATATCCTTTAGGCAGCGTAAAGCTGAATTCCGTTTGCAAAAGTTCCATGATCTCCCTCGCTTCTTCTTCTGAAAAATTCCCGTGCCTATGCTTCCGTCCGGCATTCCCGCCGGTGAATTTGATCCCCATACCGTCCATTTCATGTTTTGGCGTATTGCATCAAATTCTAAGCGAGAATGAGGAAAGGAAACTATTTCACTCTGCGCACACCTTCATGCACCAGTTCCATCGATTCTACGGAGACTTCATTTCCCTTGGCACTTAATGCGCTGACATCATATTTGATCGGCCAGGCTTCGAGGATATCCCACTGCGCTTTGTCATTGCCTTCTTCATCCACCAGGATGATCGACAAGCTCTTGCGGTTCTTCAGTGCCCCTTTGTCTTCAATCGACTTGCGCCAGTTGTAGAGCTCCAGGGAGTCGGTAAGGCCTTTTTTCAAGGTGATGTTCCCGAATTTGGTCAGTCCCGATAGCTTGCGTGCATGCGGAGCATCTATGCCCTCGCGGTAATCCACAGCTTCTGTAGAGGTATCCGGAATTGTCGCGTCAGCAAATGCTGCGGTTTGAATGCCGTCAATCACAACGCGGAAGCGGTAATTGCGGTAGGGGTCCAATCTTTTGCCGGTTGCCATAGAATAAATCTCCTCTCAATCTCTTATTTGGATAGGGTTTTTTGGCTGACCCGAATGACTACAAATTCCGCAGGCTTGACCGGTGCCACGCCGACTTCAATAATCAGCTGGCCGACATCCCGCACAGAAGGCGGATTGTTCTCCTCGTCCACTTTGACGAAAAAGGCTTCTTCCTGCGTAGTCCCGTATAAGGCTCCGTCTCTCCAGACCCGGGTCAGGAAAGCTGTCAGATTGCGCTTCACCTTGCCCCACAGGCTGGGATCATTCGGTTCAAAAACAACCCATTGGCTGCCCTCATCCAGCGATTCCTCAATATACATCAGCAGACGCCGGACGTTGACGTAATTCCATTCGGAATCGGAGGACAGGGTTCTGGCCCCCCATACGCAAATGCCTTCCGGCAGGGAGCGGATCACGTTGATGCCGTCCGGATTGAGCAGCTCCTGCTCCGCTTTGGTGATGATCTTCTCAATGCCAACCACGGAATCAAGATAGCCGTCCGTTGTGCCTGCGGGTGCTTTGTGGACACCGCGCACGGAATCGACATAAGCATAAGTACCGGCAATTGCACCTGACGGCGGCACGAGCTTTTGCTTGCCTGTGAGCGGATCGTTAATGTAGACCCATGGATAGTACAGGGCACCGTAAGAGGTGTTGAACGAATTGCCGGAATAGTTGCCTGCACCTTCCTTGAAATCCTTGACTTCCAGCGGACTCAGTCCGTGCGGAGGGTCAACAATGAAGATGCAGTCTTTTCTCAGCTTGCAGTAATTGAGCATGTCCAGGATCGTGCCCCGGCTGTAAGCCATATCCGCAAGGTCCGGAGCAGCCACAATGTTGATGCCGTCAATGGTGTCAAAAGCGTGGATACCTGCCCGGCTGGCTGAATCCCCCAGGAAATCGATCGGAGACATTCCGTTCACGCCGCCGCTGAGCGACAGGGCTGTTTCGTTGAAGGCCGGTGTTTTTTCCATATTTTCCAGAATGGTCAGATCGACCAGCGGCTTCACACTGACAAAAGCGGAAACCTGATTGACCTTCTCCTCAAAATTGATCAGCAGCATGTTATCGAAGACCTCAACGATTTTGCCGTCTTCATCTTCCCCGGTGTATTCATCGTTGAAGCTGCTGTCCAGCAAATACTGGACAACCATTTTGAAGCCAAACTGCTGCTTGTTGGAGGACTGGCTGATCTTCACCGAAATCCGGTTGCCCCATTTTCCTTCCGAGCGTGCAACCACCTTGAACAGATCCAGGTTATCCGTATCTTTGATGGTTAGAGATGCAGGCTGAATATCCTTAGAAGCCGCTCTTACCACGTAGCAGGAGGTGCCTCCTTCCGCAAAAAAGTTATACACGGCATAAGCCAGATAGCCATTCGGGATAAATTGGCCGAATTCATTGACGAATTGGCTCCAATTCGTGATTAGCACCGCTTTGCCGATCACACCTTTTTCTGCGATCCCTACAAACGCCCCTACAGATGTGCCTACGCCGGCAATCGGCTTGACACCGCTTGAGACTTCCTCTACATACACGCCTGGCGATAAATAATTTGCCAT

Protein sequences of DBSCAN-SWA_4

>NZ_LN831776|4939412:4961489|4945197_4945380_-|WP_020433751.1|DBSCAN-SWA
MKEQLEARMNELKAELESGRQMMQELDEKRSNLGYAMTRISGAIQVLEELSAGEEESVQD
>NZ_LN831776|4939412:4961489|4954401_4955124_-|WP_020433758.1|DBSCAN-SWA
MNEGPGITNFADSMINEGRIFGVMVGIVINNDSANHADKPGPGRVKVKIPLMGMPESNWARMASWMAGKERGAFCLPEVDDEVLVVFENGDVNRPYVIGSLWNGKDTPPETNKDGKNNIRMFKSRSGHILQFADTEGKENITLTSAKGHVIRLDDKSGAEQIQIMDKSGKNKIVIDSKANKLSVLSGQDIEISAPGGKLSLSAKTIEMKSSADTRIEASAGMEVKAAASMTIKGATVNIN
>NZ_LN831776|4939412:4961489|4948278_4949028_-|WP_020433753.1|DBSCAN-SWA
MSSQNDYSYVQYLPRVFQQKAGESDEQFFLGRFLKAFEAMLSGKTGAAGEESVGIEALLDGLHQYFDPGRAPSQFLPWLAGWVGLELEEGLEYDGEQDNRDRALAPMQILPLPAARSTVNRNLISSIVRLYKKRGTLDGLAEYLQVYAGEEAAIQINDYEEPVRCGIGQRVGINTMVGAAEPSYFSVHVILPAYSRSILQNKVQILQEVIRKEKPFYTNSSLNIEVPKMCLGVYGRVGMETLLGGMTEN
>NZ_LN831776|4939412:4961489|4958972_4959341_-|WP_039791015.1|DBSCAN-SWA
MELLQTEFSFTLPKGYVDEAGTLHKQGTMRLATAADEITPLRDSRVQQNPAYLTVILLSRVVTSLGGLSMITPRVIEELYTSDFAYLQDMYNRINQNGSNTVHTKCPKCEQPFELELESPGE
>NZ_LN831776|4939412:4961489|4958304_4958781_-|WP_020433762.1|tail|DBSCAN-SWA
MKANILNIGAKSNWVPGYREDPYLAFNFIVEIDGISVAGFSEVSGLSIETQVERKTFGGENHKEFVFLGQTKYSDLTLKNGVTNDEYLWNWYQNVVNGVVKRRSGSICLLDHSGTPKVWWNFIEACPIKWEGPAFSASSSAVAVESLVLTHNGLYRYR
>NZ_LN831776|4939412:4961489|4959950_4961489_-|WP_039837788.1|tail|DBSCAN-SWA
MANYLSPGVYVEEVSSGVKPIAGVGTSVGAFVGIAEKGVIGKAVLITNWSQFVNEFGQFIPNGYLAYAVYNFFAEGGTSCYVVRAASKDIQPASLTIKDTDNLDLFKVVARSEGKWGNRISVKISQSSNKQQFGFKMVVQYLLDSSFNDEYTGEDEDGKIVEVFDNMLLINFEEKVNQVSAFVSVKPLVDLTILENMEKTPAFNETALSLSGGVNGMSPIDFLGDSASRAGIHAFDTIDGINIVAAPDLADMAYSRGTILDMLNYCKLRKDCIFIVDPPHGLSPLEVKDFKEGAGNYSGNSFNTSYGALYYPWVYINDPLTGKQKLVPPSGAIAGTYAYVDSVRGVHKAPAGTTDGYLDSVVGIEKIITKAEQELLNPDGINVIRSLPEGICVWGARTLSSDSEWNYVNVRRLLMYIEESLDEGSQWVVFEPNDPSLWGKVKRNLTAFLTRVWRDGALYGTTQEEAFFVKVDEENNPPSVRDVGQLIIEVGVAPVKPAEFVVIRVSQKTLSK
>NZ_LN831776|4939412:4961489|4949953_4953592_-|WP_046504546.1|plate|DBSCAN-SWA
MPNKVPTIDKRNQEQLVPELRRLIYQYCSREWTDLTELEADKKVDALVHIFTQMMGKVIGRLNQAPEKNFISFLNLIGIHPTPPRSAKVPLLFKQKPDADTSSTIPAGTRVSAQPENQAEVIFETEKDLTVIQPRLVRAVSLDPEEDQWSNQDYLFAEEPSGQRAKLFKGDSTVVHRLYLGHSELLGFEEAGSRLSVYFNKPEAALALAADAPGGAGSLPDMDWFCFDEEGNTVQLSPSMTGIKEDSAWRAVVQFDHLSGVHAKTIAGYEQAERLREWSNKWIFAELKTPITAADLMPDIEDIRLELKLVSPVPLMPDMAVNNGTSLDMGKDYYPFGDKPKVNDTFYIACSEAFSKPGSRITLKIELSDPEISKLPDTPYVRLGWEYWNGKEWLGIGSLEETLDGEAAAAGGSTRSSACLTGSGMLSFQCPGIKPLTLNGEERYWIRARITGGNYGEEAKYEYQDEEVKLGEGSIKVAQLKVTQATYAPPSIRRLSIAYSHTLEGHPQTVLTENNFSFADKTAACLAEGEYFKPFYPCAELEPTFYLGFDRDISNLPVSLFFPLNGEQLRRPVVAWEYWDGRRWLTLSVNDEIRGFTRREILQFAVPTDIAKRPLFGTEQYWIRARLDEGRFEIFPQVDAIFANAVWARNSNSVAGEIPGSSNGEENQSFQLSKTPVLPGQRLRVREAPGQGEWVPWEEVDTFSLSASDGRHYMLDRSSGTIIFGDGRNGMIPPTGTDNIECDYKYGGGAAGNVAAGAVTKIWDSFSWLDSVTNPVAADGGFDQEAAEQAQIRGPHTLKSWDRGVTAEDIEWLVREAMPQIAKVKCLSAMNRDLEFVPGTATIIVVPETDEPKPVPSQELLSEIEAYLCERTSAALDTSDPGIEVIGPDYVRIGVEAAVAFTSVEQRKVEEGRIIDNLKQFFHPLYGGDRAAGWELGQNLYVSEVYAVIKNTPGVDYVSGIAIKASVQCFTASLEPLENGPYKPLAAYPKYSAVRSDDNSIQFALAERVEAGSEVKSLVLKGFKENGKIRLRYRTYEPVELIVVSIDGDILECQTLDGQPLEHSYPEGSDLEFDITDDLTVRTYILNGLASGAESFFVKIAVFEPKDIVFLSKTDEYVNTTPLKIRSIHSDNIFLEEDELIYGGTHLINKPEEHIFPYLLDKNTGLLHDLTGTTEDCRLGAILKEERKFLTGLKEAPGTAARCRYCFPEEQP
>NZ_LN831776|4939412:4961489|4959483_4959927_-|WP_019910188.1|tail|DBSCAN-SWA
MATGKRLDPYRNYRFRVVIDGIQTAAFADATIPDTSTEAVDYREGIDAPHARKLSGLTKFGNITLKKGLTDSLELYNWRKSIEDKGALKNRKSLSIILVDEEGNDKAQWDILEAWPIKYDVSALSAKGNEVSVESMELVHEGVRRVK
>NZ_LN831776|4939412:4961489|4955120_4956164_-|WP_020433759.1|DBSCAN-SWA
MGTSVANYKIELNGSKLSAELAAAVEGVTLEDEINLPALFSIQMNMVNSGSGMWRGTDLKSIKPGDKVKLSLGLDKLQPMISGEITALDLNFGEHSVLDIRGYDLLHRLRMGTRSKAFLKKKDSDIASEIAKEHGLTPVVDDTGTVYPYIFQNNQSNYEFLVERAAMLDYELYADDKKLYFVKSRSVKAPGLPELSFKKDFERLNLELRALTRGSKVKVKGWDVKEKKELEAEAKTGDETTKMGGTESGFSLSAKAIEESPVAIMAEHLLDMSEAKTLASAAYNSRLRDFIAGEGMCWGNPQLRAGQTVKLLGLGERFSGIYYIVSTVHKIDSKGYTTTFRVKRTGL
>NZ_LN831776|4939412:4961489|4956176_4956788_-|WP_020433760.1|DBSCAN-SWA
MAEKAKIIPLDMPVGAIEVMFNPNEYTVSFEGKYTGEKNNKQFQITETPELKVSLFYDTYEKRTDVRKKTKLLTSLLDPKVSGKNTKKPPVCLFVWGGFTYRGLLSKIEQKFTMFMENGTPVRSLLDVTFITEESDKTVEDNRGLNACRKLWVVKSGDRLDLIANEALKEPLAWRRIAELNKIVNPIGFPGKNDIGRTLVIPD
>NZ_LN831776|4939412:4961489|4939412_4945160_-|WP_046504538.1|tail|DBSCAN-SWA
MPKDMKRMNYFNGLLLKEEDLTLDQNYHKRARGLHNRYFHNWGVVTGLKVNPKELTQVEIDPGFALNRITDPDNNEEISQEILVSDTHPKRVLDLSGYSTSDQIYISVSYMEELADPDLLKGGGENIHVWEKADIKASSLKPKDVRKDILLGRVTLKHNQDGALSIDQIYDTDVDGTQLVTRAIGGETLKADKIIVGSKEDPDQPFLSNSVKEDGKEGNKLNVHAALTEFTGNLRTGAISSYGALDVNGELAVTAGSEQVFKVNDSGDVDMSGSVAVAGSFSAKSGIEVSGGMAVLDVPQVMVGGNMVTLNKNASKENNSGFEVIRKDEPSAKLLWDEKSKGWMIGTDVKEGDAASGMFHVAYGAEWEQLHGGSLADGLHSHSQLHSADGKPALRTDAQGNIQIDQTLTVSGSLVSKQDGLEVFRGETLPNAKIAWNETAKSWQIGTANGDMTDIPDGKQWEELTGGTGNADALHTHRQFHNEDKSLLALEIGADGNVNIPHELMVGETLTVNKLIVREEEVVVKKVEQEVADSFLTVNKADNDAVLGSKGGLDVYRGIKNPKARMEWNEAERKWKIGLEGSMSDIPYGTKWDSLTNGSLADAAHKHSALSTPSGGTILSADEHGKVSASGSLEIGGTLKGQGNSELKADLNVGGSATIEGNLTVKGKTTYVDKVDLVVASNRIELNKSESNGSILNQSSIDVYRGKQKPSARLVWSETDGRWKLGLGDELSNIAYGSNWDALTGGVSSDADGLHRHNSLSDSKGNTVIQATAKGDIEITNSAEVQGTLTVDNGADISGGLAVQGQLKVDGNLIVKGTTTTVEREDLVVTNNVIEINKFKGGTPPANESGIEVYRGESQPAARIIWNESERKWKVGTGSALENIASGSSWDKLTQMASADSLHTHSQIYNPQTDILALSASAEGDVDVHHDLTVGSNLTVAGDLEVRGTSASITTDELDIGSPWVTINKDGGEVSSLSGGGLEIYRGPNQPAAKITWDETKDEWQLATPTEPAAMVVDTSGNVNVPGGLKAANASVLGAVTAASAAIAGTVTVGDGLEVLQGTETSAQIKWAKDRWKLGTAGKTVLSLTRSGKVGVGTDNPTEVLDVAGKAVFRTEAEIAGAATFSGKVTAHGEATFEGDAAFNKAIHAADLAVSKNAVVAGNVVAGGFEAPRGLDSSGKELPNARIVWNNVQKAWFYGDGVTLSEFGTGKGGQNKLYNALGDTIALFADSEGRVGIGTNTPLALMDVKIKGGLTAFSVTGAGNVGIGTYDPKSKLDVQGDTAVAGTLTAVNAVISKDLTVTGNLTVNGDTVMINAATLEVEDNIIRVNKYAPQATPVVKNAGLEVFRGGTALPAQLIWDETADEWQAGVPNALKAIEFKGHTHPEFAELSGAFTVVSGNVGIGTPAPAAKLDVNGNVAVSGKLTAVDAAASGTLTAKDATVSGALTAKDATVSGVLTAKDAAISGSLTLGQGIAVDRGADPKAQLLWDESTDAWQAGVAGSMKQLSYSGHTHPELTALTGVLKIASGNLGIGTVAPTAKLDVNGNAVVSGKMTVVDTAISGTLTAKDATVSGSLTLSQGIAVERGTDPKAQILWNEALDEWQVGVAGSLKQLAYSGHTHQELTDLSAVLKIASGNLGIGTATPAAKLDVNGNAAVSGKLTVADAAVSGTLTAKDAALTGVLTVKDVSLSGTLTVPNATVSATLTAKDAAVSNKLTAKDAVISGSLAVSQGIEVGRGTDKKARIAWDTANNVWQAGIEDNLQTLVCKDHVYDELIQVAGAVTVDSSSNVGIGKTPTDDYKLDVNGNLRATNFAQTSSRTFKENIASLPVKKALELLNKLKPVTFNYKAENAKKQNIGFIAEDVPQIFSTTDHKSVVLMDIIAVLTTVVQKQQKEAQDMRKQVNELQVQVKALAGA
>NZ_LN831776|4939412:4961489|4949024_4949897_-|WP_020433754.1|DBSCAN-SWA
MPLPVPNLDDLGFDELVADAKTLIPLYDPDWTNYNPSDPGITLIELFAWFSEMVLYRIDQVTEESQLQFLKLLGVALAEGEELTSGIRRGVKQFSECYRAVTAADFQLLAKQSLLDIPGILDTYPDLAVRTLCLINTDMENGTGVNKEAFGHVSVVLILQTDNQKDLLREMTQIKQSVKAYLDARKLLTTRVHVVEPDYRDIVIEMTVSAKDKSIGSTVIDSITRFLDPVSGGEEGLGWLPGRKLYASDLYHLVEGISGIDHVTSVALDSPDLLPFQLFKLKDLKVEVES
>NZ_LN831776|4939412:4961489|4956787_4958257_-|WP_167345649.1|DBSCAN-SWA
MDFIQAILGKYGITRWRSRFQSLILRQYPLLFAEPEAVKPAETVINNIHPVKEMHIHHSIYPPITQVMTGPGTVNRVLYTTQGSGGAGIGSPASSPGHQNLIHGLQERVWKQQHAERPVTRGYRTLDPAGSAVEPVTVQVAMRNQERTDGTPLSYLLPMPAAAPAGTDLAGRRIGSRLEPYSGDSRQGQSLAGRGPQHLPAAHGQLQTLRTYILHQSVDTVNNEQPLRQKLEPAAVRHDQAEPPRMALSHPGAGSGSAGTTVEAQHSTPSVRPSPGPRSLVSPNLHLGLGQRLAAALDKLEGRSERLNPLPAGPAAVHDGLQQPDVLPLQLLAVPSEPRSMVQRHSSARLSSAVRPAHIGGLLSVAPQNGLIHTAKGQAVPLALKGRGPGGRLITAGPEQEEYLQPAGRYSSLILRKPAAPKAARPEPVQQWPEPVPQERAAPPTSQSFPKAAAPAAKMDTAELNQLAERVYQVLEKKMAIRKDRRGLR
>NZ_LN831776|4939412:4961489|4945398_4948251_-|WP_046504542.1|tail|DBSCAN-SWA
MGKEFARMRYFDGLFLNAEDYKLDQNFYLRLQRLHNRYLHTWGIVCGLKVLPVLDPGEYMKVKVAEGLALNQVVIEDAATKKKESISQEILIYEGHPDNPVDLSEYNANETIYIWVSYEEMETDRNIERGQGEKIHIWERGRISHGTKKPDSSEHIVLARIVPRKESNGIVIDSACIFDYDSDVARTPLRTYAGAAGKKMVTEKLIIKAKSEDSIDNMELNEATLAGMPAVYTLQEGKVLEVSAPETRFTGALNIAGDLTLQGELILQSKDKSQSEMRIMNSFVEVNSPNTDDPDYEFPGPRDGGLEVYRGDGGIHDARIVWVEADQCFKAGLGTDLKKIAYGNEWDSLIKYEFADLLHRHSKLSSSGGSSFGFNSSGKLFSDADLALKDGTTFWLKGTNPDTIDSSHGLGWFGAGKPFAASEVDGPVLFGNSGGVLGTRTANSDGSRTDRPVLSWNKAGYVGIGPRKALEDSLDIDGSLRILSGRNPVRFTSVWSGFPDNQINGAEISNDITNHKALMIVGNQSAGQGRKVAIWDRLDVNGFLYVNGVMQAAQEIIPSAGKGEHNGIIFPANPGGGGSDLAWIKYYPRSGEDCTLEIGTSNDANDHISLNASGNVGVGTLTPADKLDVAGELRVLSGKNPIRFTSAWSGFPDQAHNQAEISNDTTTYKSLMLIGNSSSPDGKRKVAVWDQLDVNGFLQVNGSARIAGDLQITGSIKTDVFNFDGRFKKLDVADNFAAYVRCADFYIGYSGRRGAPGRALVDNGNHLVLNYGNDWSYASVHSSLEVKNALIPSAGSGNNGIIFPSDPGGGSGDSAWIKFYPTSGENCVLDIGVSNDAGDRIYLHASGGVYANGSMYWWSSRELKDNIADIPVKEAKQLLDGLNPVSFKYKGSTKEKTLGFIAEEVPAVLADPDQRAISGMDIIAVLTSVVKDQQKAITRMQKQIATLQGA
>NZ_LN831776|4939412:4961489|4953591_4953987_-|WP_020433756.1|DBSCAN-SWA
MEVVDFLGRGWKYPFAVQRGSINSSDGEDSIRESILLILSTARGERVMRPDFGCRLNELVFAPNTMSTATLLRSFIEEALQNWEPRIEVDDITVTPRSDQSQLEVSIDYSIRASNSKYNLVYPFFLESVGK
>NZ_LN831776|4939412:4961489|4953990_4954386_-|WP_020433757.1|DBSCAN-SWA
MGQPAAKKGDRILATDTHIVMLPAGPAPVPTPLPHPFTGILDGALSANVKIMGQPAATVDSTATNTPAHVPQGGPFQKPPTNQGKIIAGSASVKINGKMAARHSDPALTCNDPADLPVGKVVAAGTVLIGG
>NZ_LN831776|4939412:4961489|4958790_4958976_-|WP_046504551.1|DBSCAN-SWA
MVGYPLDRLYEEVAFLTYYLHWDYAAVLNLEHPERNRWCSEVSKINQKLGGGEEKKNFFEA

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_046504538.1|4939412_4945160_-|tail	tail fiber domain-containing protein	NA	NA	NA	NA
WP_020433751.1|4945197_4945380_-	hypothetical protein	NA	NA	NA	NA
WP_046504542.1|4945398_4948251_-|tail	tail fiber domain-containing protein	NA	NA	NA	NA
WP_020433753.1|4948278_4949028_-	hypothetical protein	NA	NA	NA	NA
WP_020433754.1|4949024_4949897_-	hypothetical protein	NA	NA	NA	NA
WP_046504546.1|4949953_4953592_-|plate	putative baseplate assembly protein	NA	NA	NA	NA
WP_020433756.1|4953591_4953987_-	GPW/gp25 family protein	M4SKQ1	Cyanophage	2.0e-10	35.0
WP_020433757.1|4953990_4954386_-	PAAR motif protein	NA	NA	NA	NA
WP_020433758.1|4954401_4955124_-	hypothetical protein	NA	NA	NA	NA
WP_020433759.1|4955120_4956164_-	phage late control D family protein	NA	NA	NA	NA
WP_020433760.1|4956176_4956788_-	LysM peptidoglycan-binding domain-containing protein	NA	NA	NA	NA
WP_167345649.1|4956787_4958257_-	hypothetical protein	NA	NA	NA	NA
WP_020433762.1|4958304_4958781_-|tail	phage tail protein	NA	NA	NA	NA
WP_046504551.1|4958790_4958976_-	hypothetical protein	NA	NA	NA	NA
WP_039791015.1|4958972_4959341_-	hypothetical protein	NA	NA	NA	NA
WP_019910188.1|4959483_4959927_-|tail	phage tail protein	NA	NA	NA	NA
WP_039837788.1|4959950_4961489_-|tail	phage tail sheath family protein	J9PVC2	Bacillus_phage	6.2e-76	35.1

Sequences of DBSCAN-SWA_5

Nucleotide sequences of DBSCAN-SWA_5

>NZ_LN831776|5247547:5256690|DBSCAN-SWA
GTTACTGTTTATTTCCCGCGGCGCCTATCTGGAACAGCGCCCGCAGCGCACTGCCGAGTGCCTGCAGCCAGTTGTCTGCCGGATAGGCGGCTGCTCCTGCGTGTTGGAATCTTTTCTCATAGGGCGACTGCTCCGGAGGCAGCCGGTCCGGCATATAGACCGGAACCCGGCCGATCTCCTTGCCACCTAACTGCAGTACGAGTGCCCCCTTGATGCCAAAGCTGCTTCTTCGCGTATTCTTATTCTCCCGGATGAGTTCCAGCTTGGTCACAAGCCTCGCTTCCTCCCCCTGTCCAAGCGGATAGGCAAACGTTCTGGCAGGGACAAAGCTGTAGCCGCTGATGCCTTCACCGCGCTCGACAAGCGTCTTCAGCGGATAGTGATTGAAGCCGTAATCCAGCAGCACGGCATGGTCATTCCAGTCATTGCCGTCATTCAGCGTAACGGCGACCAGCTGCTGGCCGCCCCGGGTGGCGGAGCTGACGAGGCAGCGCAGCGCTTTTTTGGTATACCCCGTCTTTACTCCATCCGCCCCTTCATACAGGCGCAGCATTTTATTTTTGTTCAGCCACTTATAATCCCATGGCTCATACGGGTTATCCGCCGTTTTCACCTGGGTCTTCACAATCTGCTTGAATACCGGATTATGCATAGCATAGGCTGTAAGCACAGCCAGGTCATTGGCGCTGGAATAATGCCCTTCCGCATCCAGTCCATGGGGATTAGTAAAATGCGTGTGCTGCAGCCCCAGTTCCTCCGCCTTGGCATTCATCAGATACACAAAACCTTCTTCCGATCCTCCGACATGCTCGGCAATGGCTGTAGCCGCATCGTTGCCTGAACGCAGCATCAGTCCATAGAGCATATCCTCCAGCCTCATTTCTTCCCCCTGCTTCAGGAACAGGGAGGAGCCTTCCTTGGCAAAGGCATTTTTGCCGACCTTGACCTTGGACCGCAAATCTCCGTTCTCTATGGCAACTAGCGCAGTCATAATTTTGGTCAGGCTGGCAATCAGCATAGGCTCGTCCCCGCGGCTGCTGTACAGAAGCCTCCCGGACGCTACATCAATCAGCGCGGCAGCCCTGGCATGGGTAGTAATCGTACTATTCTCAGCCCGGACCAGAGGCTGGGGAGCCGCACACAGCAGCAGTGCGCACAATATTAGAACCAGCAGTACCTTAAGGTTAGATGTCTTCATGTTCATCCTCCGGCTTCTTATCTGTTCACTTGTGTTGTACAAGTGTATGCGGGGCTACGGGATGGTATGTCCATCTCTTCCCCACAAGCTCTATCATCACAAAAAGGGACACCGCCTAGTGAGGCGATATCCCTGTTGTCTGCCGCTGCATCCTTCAGGTACATCCCATAACGCTAATGAGTCGAGGAATCTGAAGGGACAGGGGTTTTAACCGCTTTTTCGGTACCCGAAGCTACTACTTGTGAACCTACAGGTGTGCCATTCTGCGGCGAAGCGTCATTCTGGGACGATCCGCTGCTTGGGAACATGGTCTGAATTTTGTCGATGAGACCCGGAGTCGCATCAATAATTTTCTCGAACAGATGGGTCTGGTTATCCAGCGGCACAATGTGAACCCCTTCCCTGCCGACCACAAGAAAGGCGATTGGCCGGATGGATACCCCGCCGCCGCTGCCGCCGCCGAACGGAAGCATTTTGACGCCGCTTCCAGCGCCATTGATGCCGGGGGCATCATCTTCGACACGGTAATCACTACCGCCTGCGGCAAAGCCGAAGGCAACTTTACTGATCGGCAGAATCACACTGCCATCCGGAGTTTCTACCGGGTCGCCGACAATCGTGTTGACATCCACCATGCCTTTAATATTTTCCATAGCGGTCTGCATGAGACCTTGAATCGGGTGCTCTGACATCTAAGTACTCCTCCTCTGCTGTTTGAAAGATAAGGGAATTACCTACTCTTGTACAGTCTGCTCATATATCGGGCATGATATGTACGCACTCTAATAAAAATACGGGCGAAATAAAGCTGCCGGCTGGCGCTCTAGCCAGAAATAACCTTCGCAATTTCGCCTCACATAAAATCCGCTTAAGAGGCCAGAATGATGGCTAAGCAGAAAAATGTGCATAAGGAGGCTGAGCTATGGATTTCGCGAAAATTTGGCAGGCGGATATGGAAGGCAACGGCTTGCTGCCATTGATTAAGGGCGGGAGCGACACGCAAAAAGACCCCCAAAAGGGATACGTGATCGTAAACCTGAATCCGCAGGATGGCGAGGCTGGGGGCGGGAACGGGAAGAATCAAACCACCGTTTTTAAGGAGGTCGTTATCCCTGACGGCAAACGGTATAGTTATGATCTGTTCAGAAAGCTGAAAAATAATTACAAATCGGTGTCCGGCGGGAAAGATGCGGTTTCGGCTGCAGAACATGAGCAAATTCATGAATTTCTGGCCTATGCCGCAGTGTCGGCACCTTTACGCCAGGCCCGCAAGTATGCCGAGGATCACCATCAGATTAAGGCCGGATGTTCCAAAGAAGAATGGGTGGAGACGCTTCGATCGATCTGGTTCCAGCCCAGTAATGACGGCACCTCATTTTTTGAGCATGTTTTTATTGGCGAGCAGGGCAGCAAATGGGGCGGACATCAATTCTGGTACAGCTACCATTTGAATGAGGGGCCTGATGAGACTCTTCAGAAAGAGGATTCTAACATTGTTATCAAGCTTGCCGAGGCTAGGCAGACTGTTAAAAGCAGCCTGGCCGAAGTTATCTCCATAAAATATACACTGGAAGAAACCAGCAAGAACGGGGACAAACAGACCCTGACCACAGATATCGGCGGATTGTTTGTCGGGATCAGTGCGGAAGGGCTGATGGCTCTGGGAACAGTAGCGTATCTGGATGGCCGGGCCCGGATTCCTGTGGAGCTTAACGGTACGTCCTTTGATCTTATTATGCACAAAACGGGGGACCGCGAAGAGAAACCGCAAAGCTTCTACCCTCAAATAAAAACACCTGTTCACGCTTAATGTCCGGAACAGAATTGAAAATTCCCGGCAGCCCGCAGACTCCCTGCGGCGCTGCCTTTTTGTGCGGAACCGCCGCAGCCGGCTTAATCCGCTTCCTCCTCTGAGGAAGCCTGGGGGCTGCGGCTAAGCAGCTTTTTCCAGTACCGCAGCCCTCCCGGTACCTTGGAGGCCCGCCGCAGAAGCTGAAGCCCTGAATAAAAGGCATAGCCCATTGAAAGCTTACCCGCGCATACCGCCTGGGTGGAGAAGGACAGCTCATCTGAGAACACGGGTGCAACGAACATCCGCGGAGCTTTGATCAGCCGGACCTGCCTTGATAACCAGCCTGCCAAAGTCCATTTCAGCCCCCAGAACGCTCCCGCTGCCGTCGCCGTATATGCCGCATCGCCCATTGAGAAATCGGTAGACCAGTCAAGCTTGGTGATCTGGACATGGGCCAGTGTATCCTTCAGCCATTTGTTCAGACCGCGCGTTGCCTTCATCGCTATACGGATATTCTTCAGCCATTCCGCAACCGACTGCTTGTCGATTTGCTCTTCAAGGTCTTGATCCTTCCGGACCGGCGCAATGCCGCTTTCCTCCAGCTTGACTTTGATCCCCTTCTCAATTCCCTGGAACACGAGCGCAGGCAGCTCATAGTGAAATTTGACCAAGCCAAATAGAGCTTTCAGATCTAACTCTATCCGGTCATCTTTGCCCAGCCTGCACACCCGGAAATGAAAATGTATGTATGAAGTCAGAATCACCAGCAGCACTACAATCACTAGCAGCAGCAGCGCCAAGGGTATTGCCAGCCATAACGTCACGAAAGTAACCTCCATGCAACCAATAATAAGGAGCCTTTGAATTAGTATGGCATTCAGGGCTGGAAAAAATTCCGCGCTCATGCAAAAAAGCCCCATAGCCCATCCCTGATGCCTGTGGCATATAGATGAATGGCTATAGGGATTTTTGTTTTTCATGTTCGCTTTATATAGCTTCTAAAAATCCGGCGGCTCAAGTCTGCTCCGTATCCTCAAAGGTCATCTGGCTGTCCAGCTTGCTGAACAGGAGCTGTGTCTCCTCTTCCAGGTCGTCGGTGGAGGCGTCGAAGTTTGAAGGCTCCGGCAGCTCCTTCAAATCGGCCAGCCCGAAACTCTCAAGGAACGATTTGGTGGTTCCATACAGAATAGGGCGGCCCACCGCTTCCGCACGCCCGACCTCCTGGATCAAATCCTTGTTGTTCAGTGTATGAATGGCCCGTTCAGACTTCACTCCGCGGATCTCCTCAATCTCCACACGGGTAATCGGCTGACGGTAAGCGACGATGGCCAGTGTCTCCAGCGCTGCCTGGGACAAGGATGCGCGTGAAGGTGAATAAGCGAGCCTTTCGAAATAAGGCGCATGGTCTGGCAGCGTAGCCAGACGGTAGTTCCCGGCAATCTGCACGACCTGCAGGCCGCGTTCATGGGACACATAATCCTCTTTCAGCTCCTGCAGCGCTTTGCCGGCAATATCCGGCCGCTGCTCCGTAATTTCGGCGATCTGGCGGACAGACAGGCCTTCATCGCCGGACAGGAACAGCAGGCCTTCAATAATTGATTTCAGCGTTTTGAATTCCACTGAGATCTCCTCCTCCTCTCCACTCCATTACAATGTCATCAAATAATTTCTCCTGGTAACAGAATATGGCCTTCATTTTCATCAGCTCCAGAATAGCAAGAAAGGTAACCACAATCTCATGCCGGGCCATTTCATCATCCAGCAGCGCGGAGAAGCGCATTCTGCCGCCTGTCCCCTTGCGCTGGAGCGCTGCCGAGACATCGCGTATCCGGTCTTTTACGGAAATTTCATCCCGGGTAATCCGCTGGTAGGAGGATCTCCGGGCCGCTTTGCTCAGCGCCTTCCGGAATGCGGCGATCAGGTCTGCAGTATGCAAGCCCTTTAGCGTATTATCGATTTGGGCCGGCACAAAAGGACCCAGGTCCTCCGGCTCCTTGGTGAAGATCAGGCTGCGTTCACTCTCCATATCCAGCAGCTGCACGGCAATGCTCTTGAACTTGCGGTATTCGATCAGCCGCTGAACCAGCTCTGCACGCGGATCATAATCGTCGTCCTCGTAATATTCGAAATCCTCGATTTCAATAACCGGCGGCTTCGGCAGCAGCAGCTTGCTCTTGATCGACAGCAGCGTTGCAGCCATCACTAAAAATTCACTGGTGATATCCAGCTCAAGCTCCTGCATCGTCCTTAGATATTCCATGTACTGCTCGGTGATCTCGCTGACCGGAATGTCCTGGATGTCGATTTCCGCCTTGTCTATTAAGTGCAAGAGCAAATCGAGCGGACCTTCGAACGTCTCCAGCTTGTACAATACAGTCACGCGGTTTCCTCCCGCCAAAAAAAAGTAAAGTGCAGCGCCGCACGGGCGCTACACAAGTAGAAAGATCTTATGGTTCATGCTTTCTTCTCATACATATAAATAAGCACGATTTTAGCTGATTCGTCAAGAGTCTCTTATTCAAGCAGAAGCATCTTATTTTTTAAACAGCTTGTTCAGGTTCGCCATTTCAATGGCAGAGGCCGCAGCATCCCAGCCTTTATTGCCGGCCTTGGTTCCGGAGCGCTCAATCGCCTGCTCGATATTTTCGGTAGTCACTACGCCAAAAATGGTTGGAATACCGGTCTTCAGATTGATGGCCGCCACCCCTTTGGCTACCTCGTTGCACACATAATCATAATGGGTTGTTGATCCGCGAATGACGGTTCCCAATGCGATGACTGCATCGTATCTGCCGCTTTCCGCCATTTTCTGGGCAATCAGCGGAATTTCGAACACGCCCGGAACCCAGGCCACATCCACTTCATCATCAGCTACACCATGACGCTTGAACGCATCCAGCGCACCGGACAGCAGCTTGCTGGTAATAAACTCATTAAAACGCCCTACTACTACCCCGTATCTCAGTCCCTCGGATACTAAATGTCCTTCTAAATAATTCGGCATTGTATTCATCAACCTTTCATTAGTAAGTGATTATGGAGGTTACAGCTTGGAATCCTCATTTTGCTCGATGTTGTCAAAAGTCAGCAGATGGCCCAGCTTGGCCTGCTTGGTATGGAGATAGTTGGTATTGTCCTTGTTCTCCGGCATTTGGATCGGCACACGTTCCACAACCTCAAGACCGTAGCCTTCCAGTCCTTTGATCTTGCGCGGATTGTTGGTCATCAGTTTGATCTGGCGTACCCCCAGATCCTTAAGAATCTGGGCGCCGATGCCATAGTCGCGCAGGTCTGCCGGGAAGCCCAGCTTCAGGTTGGCATCCACCGTATCCAGACCTTCCTCTTGAAGCTTGTAGGCGCGGAGCTTGTTGATCAGCCCGATGCCTCTGCCCTCCTGGCGCATATAGAGCAGAACCCCCCGGCCTGCCGCTTCAATCTGGCGCAGCGCCGCTTCAAACTGTGGGCCGCAGTCGCAGCGGTGAGAGTGGAACACATCGCCGGTCAGGCATTCGGAATGAACACGGACCAGCACCGGCTCTTCACCGGAAATATCGCCTTTGACCAAAGCGACATGTTCTTTGTCATCTACTTCATTCGTATAGGCGATCGTCTGAAAGTCGCCGAAATCCGTCGGCAGCTTGACCGAAACCTCACGGGTGACCAGCTGCTCCTTCTCATTGCGGTAATGAATGAGATCCTTAATGCTGATCAGCTTGAGCTCATGCTTGCGCGCAATCTCCACCAGATCCGGCAGACGGGCCATGGTCCCGTCTTCCTTAACCACTTCACAGATTACGCTGGCCGGATAAGCGCCGCACATGCGGGCCAGGTCCACAGCAGCTTCCGTATGTCCGGAGCGGCGCAGCACACCGCCTTTTTTGGCAATCAGCGGGAACATATGCCCCGGTCTGCGGAAGTCGGAAGGTTTGGCCTCCGGGTCCATCAGCGCCTGAATGGTTTTGGATCTTTCTGCGGCTGAAATACCTGTGGTGGTATCCTTGTGATCGACGGATACGGTAAAAGCTGTGCCATGATTGTCGGTATTATGTGCAACCATAGGCTGCAGATCCAGTTCTGCCGCCCGCTCTGCCGTAATCGGCACACAGACCAGCCCGCGTCCCTCTGTAATCATGAAGTTGATCACTTCCGGTGTGGAGCGTTCGGCCAGTGCGATGAAGTCCCCTTCATTTTCGCGGTCTTCGTCATCCACTACGATAATGACCTTGCCGCGCATCAGATCATAAATTGCGTCCTCAATCGGGTCCAGGACGCTGTCGTTCTTGATTGGCTGGCTCATCTTTCTGTCCTCCTGACAGCTTGGCGTACCCTAATAAGGGCTTAAGCGCAAGCCTGCTCTTTATTTATACAAACCCGTTCGCCGCCAGAAAATCACGGCTGATCCGGGAGCTGTTCGCTTCTTCCGCATTCCCTGCACGTGAACCGTAGTTAAGGAGATGGTCCACATACTTGCCCAGCACATCGCATTCCAGATTGATCCGGTCCCCGGTCCGCTTGTGGGCCAGGACCGTTTCACCGAGCGTATGGGGAATGATGGATACGGTAAACGCAGAAGCTGAAGTGTCGACGACGGTCAGGCTGATGCCGTCAATGGTAATGGAGCCTTTGGGAATAATGAATTTGAACAGCGATGTACGCTCTGGAGCAATCTCGAAGACGACCGCGTTCTGGTCGCGTTTGACGCTGCGGATTTCCCCGGTTCCGTCTACATGGCCTTGCACAATATGTCCGCCGAAACGGCCGCCGGCCGCCATGGCCCGCTCCAGGTTCATTCTGCTTCCGCTGCGCAGCTCCTTCAGTGTGCTGTTCCGGTACGTCTGAGGCATGACATCAACGGTAAAAGAATGATCGCCGATGGAAGTCGCCGTGAGACAGACGCCATTCACCGATACGCTGTCGCCGATTTTCAAGTCATCCATAATGAGGGATGCGCCGATGTTCAGCACCATCATCTCGCCTCCGCTGGTCACCCCGCGCAGCACTCCGACCTCTTCAATTAAACCTGTGAACATGTGATCGCCTCCTGATATTTGCTTTAGCGGATAGGCGTGCCGCTGATACACACATTATCCCCGAGCACTTCCACTTCCAATCCTTCCAGTGTAACCGCGCTTTGCATCAGCTCTACACCTGGAAAGTCGAAGGTTCCGGGTGAAGCTGAGCCGCCCCCTACGATCTTCGGGGCGAAGAACAGGACCACACGGTCCACCAGACCGTTCTCCAGCATGGCACCGTTCAGGGTTCCGCCGCCTTCCAGCAGGATCGAACCTATCTCCAGCCCGCCAAGACTGGTCATTGCCGCCTTGAGATCCACCCGCGGCCCGGCGCCGCTGACAACGATCTGCACCCCGGCATCGAGCAGTGCTGCCCGCTTCACAGGATCAGCAGATTCGGTAGTGACGACAATGGTGGGCGCCTGGCCATCACGGACGACAGCAGAATCAAGCGGAATCCGCAGCGTAGAGTCAATCACGATCCGGACCGGATTCAGTCCCGGCACTTCCATCCTCGTAGTCAAGGAAGGATTGTCGGCAATCACGGTGTTGACGCCAACCATAATTCCTTGGTGGCGGTGCCGCAGCGTGTGCACAATCTCCCGCGCCTGTCCATTGGATATCCATTTGCTGTCCCCGGTCCGGGTGGCCAGCTTCCCGTCAAGCGTGCTGGCGCTCTTCAGCGTGACAAAAGGCTGCTTGGTCAGAATATACTTGATGAATTTCTCGTTCAGCCGCAGAGCCCGGCTTCGGAGCAGCCCCACCTCAACCTCAATTCCCTGCTCCCGCAGCATGGTGATGCCACGCCCGGCAACCTGGGGATTGGGGTCCTCACAGGCCACAACCACGCGGGCAACCCCTTCATCAATCAGCCTCTGGCTGCAGGGGGGTGTCTTGCCATAGTGGCTGCAAGGCTCAAGAGTTACATAAGCCGTGCTTCCCTGCGCCTTGCCCGCCGCCATATTCAGCGCGTGCACTTCGGCGTGGCCTGTCCCCCGCTGCAGATGGGTGCCGAGGCCAATCATGGCTCCATCCTTCACGACAACACAGCCGACTACGGGATTAATGCCAGTCTGGCCTTGCGCTCTTTCCGCCATATCCAGTGCGAGCGACATATAAAACTCGTCGTTCATTGTATCCAT

Protein sequences of DBSCAN-SWA_5

>NZ_LN831776|5247547:5256690|5255589_5256690_-|WP_020427533.1|DBSCAN-SWA
MDTMNDEFYMSLALDMAERAQGQTGINPVVGCVVVKDGAMIGLGTHLQRGTGHAEVHALNMAAGKAQGSTAYVTLEPCSHYGKTPPCSQRLIDEGVARVVVACEDPNPQVAGRGITMLREQGIEVEVGLLRSRALRLNEKFIKYILTKQPFVTLKSASTLDGKLATRTGDSKWISNGQAREIVHTLRHRHQGIMVGVNTVIADNPSLTTRMEVPGLNPVRIVIDSTLRIPLDSAVVRDGQAPTIVVTTESADPVKRAALLDAGVQIVVSGAGPRVDLKAAMTSLGGLEIGSILLEGGGTLNGAMLENGLVDRVVLFFAPKIVGGGSASPGTFDFPGVELMQSAVTLEGLEVEVLGDNVCISGTPIR
>NZ_LN831776|5247547:5256690|5247547_5248750_-|WP_039787129.1|DBSCAN-SWA
MNMKTSNLKVLLVLILCALLLCAAPQPLVRAENSTITTHARAAALIDVASGRLLYSSRGDEPMLIASLTKIMTALVAIENGDLRSKVKVGKNAFAKEGSSLFLKQGEEMRLEDMLYGLMLRSGNDAATAIAEHVGGSEEGFVYLMNAKAEELGLQHTHFTNPHGLDAEGHYSSANDLAVLTAYAMHNPVFKQIVKTQVKTADNPYEPWDYKWLNKNKMLRLYEGADGVKTGYTKKALRCLVSSATRGGQQLVAVTLNDGNDWNDHAVLLDYGFNHYPLKTLVERGEGISGYSFVPARTFAYPLGQGEEARLVTKLELIRENKNTRRSSFGIKGALVLQLGGKEIGRVPVYMPDRLPPEQSPYEKRFQHAGAAAYPADNWLQALGSALRALFQIGAAGNKQ
>NZ_LN831776|5247547:5256690|5248917_5249436_-|WP_020427525.1|DBSCAN-SWA
MSEHPIQGLMQTAMENIKGMVDVNTIVGDPVETPDGSVILPISKVAFGFAAGGSDYRVEDDAPGINGAGSGVKMLPFGGGSGGGVSIRPIAFLVVGREGVHIVPLDNQTHLFEKIIDATPGLIDKIQTMFPSSGSSQNDASPQNGTPVGSQVVASGTEKAVKTPVPSDSSTH
>NZ_LN831776|5247547:5256690|5253069_5253540_-|WP_020427530.1|DBSCAN-SWA
MPNYLEGHLVSEGLRYGVVVGRFNEFITSKLLSGALDAFKRHGVADDEVDVAWVPGVFEIPLIAQKMAESGRYDAVIALGTVIRGSTTHYDYVCNEVAKGVAAINLKTGIPTIFGVVTTENIEQAIERSGTKAGNKGWDAAASAIEMANLNKLFKK
>NZ_LN831776|5247547:5256690|5250637_5251360_-|WP_020427527.1|DBSCAN-SWA
MTLWLAIPLALLLLVIVVLLVILTSYIHFHFRVCRLGKDDRIELDLKALFGLVKFHYELPALVFQGIEKGIKVKLEESGIAPVRKDQDLEEQIDKQSVAEWLKNIRIAMKATRGLNKWLKDTLAHVQITKLDWSTDFSMGDAAYTATAAGAFWGLKWTLAGWLSRQVRLIKAPRMFVAPVFSDELSFSTQAVCAGKLSMGYAFYSGLQLLRRASKVPGGLRYWKKLLSRSPQASSEEEAD
>NZ_LN831776|5247547:5256690|5252124_5252916_-|WP_046504742.1|DBSCAN-SWA
MTVLYKLETFEGPLDLLLHLIDKAEIDIQDIPVSEITEQYMEYLRTMQELELDITSEFLVMAATLLSIKSKLLLPKPPVIEIEDFEYYEDDDYDPRAELVQRLIEYRKFKSIAVQLLDMESERSLIFTKEPEDLGPFVPAQIDNTLKGLHTADLIAAFRKALSKAARRSSYQRITRDEISVKDRIRDVSAALQRKGTGGRMRFSALLDDEMARHEIVVTFLAILELMKMKAIFCYQEKLFDDIVMEWRGGGDLSGIQNAEINY
>NZ_LN831776|5247547:5256690|5254897_5255566_-|WP_020427532.1|DBSCAN-SWA
MFTGLIEEVGVLRGVTSGGEMMVLNIGASLIMDDLKIGDSVSVNGVCLTATSIGDHSFTVDVMPQTYRNSTLKELRSGSRMNLERAMAAGGRFGGHIVQGHVDGTGEIRSVKRDQNAVVFEIAPERTSLFKFIIPKGSITIDGISLTVVDTSASAFTVSIIPHTLGETVLAHKRTGDRINLECDVLGKYVDHLLNYGSRAGNAEEANSSRISRDFLAANGFV
>NZ_LN831776|5247547:5256690|5253579_5254833_-|WP_020427531.1|DBSCAN-SWA
MSQPIKNDSVLDPIEDAIYDLMRGKVIIVVDDEDRENEGDFIALAERSTPEVINFMITEGRGLVCVPITAERAAELDLQPMVAHNTDNHGTAFTVSVDHKDTTTGISAAERSKTIQALMDPEAKPSDFRRPGHMFPLIAKKGGVLRRSGHTEAAVDLARMCGAYPASVICEVVKEDGTMARLPDLVEIARKHELKLISIKDLIHYRNEKEQLVTREVSVKLPTDFGDFQTIAYTNEVDDKEHVALVKGDISGEEPVLVRVHSECLTGDVFHSHRCDCGPQFEAALRQIEAAGRGVLLYMRQEGRGIGLINKLRAYKLQEEGLDTVDANLKLGFPADLRDYGIGAQILKDLGVRQIKLMTNNPRKIKGLEGYGLEVVERVPIQMPENKDNTNYLHTKQAKLGHLLTFDNIEQNEDSKL
>NZ_LN831776|5247547:5256690|5249666_5250554_+|WP_020427526.1|DBSCAN-SWA
MDFAKIWQADMEGNGLLPLIKGGSDTQKDPQKGYVIVNLNPQDGEAGGGNGKNQTTVFKEVVIPDGKRYSYDLFRKLKNNYKSVSGGKDAVSAAEHEQIHEFLAYAAVSAPLRQARKYAEDHHQIKAGCSKEEWVETLRSIWFQPSNDGTSFFEHVFIGEQGSKWGGHQFWYSYHLNEGPDETLQKEDSNIVIKLAEARQTVKSSLAEVISIKYTLEETSKNGDKQTLTTDIGGLFVGISAEGLMALGTVAYLDGRARIPVELNGTSFDLIMHKTGDREEKPQSFYPQIKTPVHA
>NZ_LN831776|5247547:5256690|5251550_5252156_-|WP_020427528.1|DBSCAN-SWA
MEFKTLKSIIEGLLFLSGDEGLSVRQIAEITEQRPDIAGKALQELKEDYVSHERGLQVVQIAGNYRLATLPDHAPYFERLAYSPSRASLSQAALETLAIVAYRQPITRVEIEEIRGVKSERAIHTLNNKDLIQEVGRAEAVGRPILYGTTKSFLESFGLADLKELPEPSNFDASTDDLEEETQLLFSKLDSQMTFEDTEQT

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_039787129.1|5247547_5248750_-	D-alanyl-D-alanine carboxypeptidase	A0A1P8VVG5	Erythrobacter_phage	3.1e-06	33.3
WP_020427525.1|5248917_5249436_-	sporulation protein YtfJ	NA	NA	NA	NA
WP_020427526.1|5249666_5250554_+	hypothetical protein	NA	NA	NA	NA
WP_020427527.1|5250637_5251360_-	DUF2953 domain-containing protein	NA	NA	NA	NA
WP_020427528.1|5251550_5252156_-	SMC-Scp complex subunit ScpB	A0A1B1IVT7	uncultured_Mediterranean_phage	7.0e-15	30.3
WP_046504742.1|5252124_5252916_-	segregation/condensation protein A	A0A1B1IVW1	uncultured_Mediterranean_phage	4.9e-08	36.9
WP_020427530.1|5253069_5253540_-	6,7-dimethyl-8-ribityllumazine synthase	A0A2H4PQS3	Staphylococcus_phage	2.3e-42	56.7
WP_020427531.1|5253579_5254833_-	bifunctional 3,4-dihydroxy-2-butanone-4-phosphate synthase/GTP cyclohydrolase II	A0A2H4PQS2	Staphylococcus_phage	2.9e-116	53.2
WP_020427532.1|5254897_5255566_-	riboflavin synthase	A0A2H4PQS5	Staphylococcus_phage	5.0e-38	40.3
WP_020427533.1|5255589_5256690_-	bifunctional diaminohydroxyphosphoribosylaminopyrimidine deaminase/5-amino-6-(5-phosphoribosylamino)uracil reductase RibD	A0A2H4PQS8	Staphylococcus_phage	9.7e-55	36.1

Sequences of DBSCAN-SWA_6

Nucleotide sequences of DBSCAN-SWA_6

>NZ_LN831776|7070941:7123388|DBSCAN-SWA
ATTATTTTTGAGTGGTTCCCGGGCGGTCATTGAAGGCTAATTCAAATAAACCTGTCGCGGATAATCCGGCAAGCCCCCCTGACCATAACCGGAGCGTAAGCCCCAGATCGGTAAAAGGATACGCAGCAGCCCCTATGAGCAGCCCAATCCCAAGTCCGATAAAAGGCACGGCATTGCGCGGAAGATTGATATTATTTTTGATCAACTGCACCAAGGCAAGTGTAAATACCGCTAATACCGATGCAAAAGCCAATACATTATCCAGAATACCAGTTTGGATCATAAAAATCACTCCTTTAAGTTTCGCGTTTACCGCTCAAGTATGTTAATGTTTCCAATTCAGGGTAAGTATTGCTGATTATTCATAATATACAGCTGCGGTTATTCTAGCGGCCACTTGTAATCTCAACGGTTCGGGTAACCGGATCATAACCGACTGAAGCTCCCAGCGCCTCCGCTACAGCACGTACCGGCACATAAGTTACACCGTGCTCTAACCGGCCGTCGGCTATTTTTGCGCCATTTACTTTTACTATGGTAATCACATCACTATTCAGATTCTGTTCCTCCTTAGTCCTTCCGTTGATTAGCTTATACGCCGCTTCCACCGCTTGTACTGAAGGCTGTGCTCCCGCTCGCAGCTTGGAAAGCGTCAATCCGAAGCTCATCTGAAAATGGGGATAATCCTTCAGACTCGTCCAGTCTCCACCCCATTCAAAACCCAGCCGCTTAGCCTGCTGCACCACCTCCAGCCAATCCGCTGCCTGATCATTGTCTCCGTCGCGCGCCATGTCCCAGGACACGCTTGAGCCATTCGGCAGCAGCAATGCAAAATCAACCGCCAAGCCATAATTGTGGTAGCTCTGTCCTCCCCGGGCATTAGTAACAATCGCCCCCGACTTCGTGCGTCCTTGAGCATAGAGCGCATCCTGCTCAGCAGCCGTCCGGAGCCCTTGCGTAATGAGGATCGGGACACCGCAGGCGTAACAGCGTTCGATTAGAGCACCCACTGCTGCGAGTACGACGGGATGCAGGCCGATTAGCCGGGGAGCGGATTTATTTTTGATTTGTGTCAGGGTCAGCATGGCTTGCTCCTCCCTTCTTGCCCTCCTGGAGAACAATGAACAAATCCTGACGTTTCGTGAACACCAATAAGGTTAGGATGAGCAGCCCAATTGTGGTTCCGGTCTGGGCAACCGCCAAGGCCTCTGTTTGGAGTGATGCCAGCACAGCACCTGCTCCAGGCACTGCGGTGAAGCGAATCCACAAGGCGATTGCCATTTGGACGGTGTAGGCACTCAGAAAGAAAAAGGCTGCCACCATAAACAGGCTGACCGCCTTTGCCCGCAGACGTCTGCGAAAATACAAAAAAAGCGCAGCTATCAGCAGCAGCGCACAAATCAAAGACATCGAATATGCAATTAACAGCAAAACATCAATTACGCCCATTGTTGACACCCCGATCATAGATTAGAAATTCGGCAAATCCGTTATTTTGGATCTCCTCCTGAATCTCTTTGGATACGTCCTTATATCGAAGGATAGAGAACATTACCCGGGCCGAGGCTTGGGTCAGCTCCCTTTCCTTTTCCCGGTGCAGGGGCGATAATCGTTTGATCCATCTACTCAGCACGTTATCCTCCCCGATCTTCTTCATTTACTACATTCACACCGCTTGATGTGTAATCAACTTTCAGTCTCTGCAGCACTTCAAGCGTGGGTGCCATGAAATCTGAGCGCTCTTTATCCAGAATATTTTGCAGACGGTCCCGGTCTTCTTCAGCCCGTTCAAGCAGTTCACGCGGCACCAGATTCCCTTTGACAATCGAGCGCAAAAGCACCAGAACAATCACCAGCAGGATCAGGGCCACGATATAAGCCAGCCCATATTTATCAGCCAGGGGAAGAATTTTCTCCAAGTTTGCTACGTCGTTGCTGTTCATTGTTTCACCCCTTTCTTTTTATATTAACTGAACTTGTGATTTTTCTATTTTGGGATTGGCCGTGACTCCAGAGAATGTTTGGACTTCCAGCCGCTGTTGTCTGCAGATTTCTTGAATGTATACCGTTTATAACGGTTGAAATCCGCAGACAAAGGCGGACGCTAACGCTCCTACAGTTCCAAACTTCCCCTCCGCACTTCTACCCTTTTATTCATTTTTCAAGTTCATTATATATTGATGTACAAAAACCCCCGGGTCCCCGGGGGCAAAATAAAAACGCCATAGCAGGCGCTAGCGTTTATCTATACTTCTTCAGTCAGGAACTCAAGTCCGTTATCCACCAGGATTTCTTTTACGCCAGCTTTCAATATTGCTGGAACTTCAGCGAACTTGGTTTTCCCCAAGATTACACGCTGTGCGAAAAACATAGTCATTAAAAATCACCTTCTTCCCATTTTGACCTTCAACCATATAGAGCAGGCTGGTTATTACTGATAGACCCTCATCGCCATCTCTGCAATGATATCTTCAATAAAGTCAGCCCTCTCAGACAGAGCATTGTTTTGCGACTTCAGCAGAAGATTTTCCTTTTGGAGCTGTTCAAGCCCAGTAAGTTCCGGCGGCTTGTTGGCTTCGGCTTCCTGGTAGGCTTCCCAAGCGGCTTGCAGCTCGGCTTCTGTCGGCTGGGGCTTATCCAGGTTCCAGACTGCGATATAGGGTCCACGCTCTACGATATCGTAATCCTCACCCTCAGTGAGTAGGTTGTAGTCGATACCGTAGCGATAATGGACGTCCTCTGCTGGTTTCTCGCCTTCTTTCGGCGGCTTGATCTCGTAGCGGACTCGGCCTTTTTCCTCGGCTCCGGGCCGCAGGATGGGTTCCGGGCCGTTGTCCCATACTTCAAAATCTTTATTCGGTTCCGCCGTTGGAAACAACTGTTCTATAGCAAGCGATAAAATCATTTCATCATCTCCATTCTTTTTATGCAACTCGCACAATTTCAAGGTGGGTTGTATCCATGCCATTTACTATGGCAACGGAATACATGTCTGTGTATAGCTGTATGGCAGCAGTCTGTCCAGCTGGGAGATACAGGAATATGTCTCCTGATAAGAAAGTATGTGTGGTCACAGTCGTTGTTAAAACATCCGCAATCCATCTGCTAGAACCATTTTGCAGTATACCGAGTTGATAAGTGGCAGCCGGGGCACTCTGTAACTGGACAGCCGCTTTGATTTTATACCAACCTGTTTGTGGACTAGTGAATACTCCCGTAGTGGTGTTGTACCCGCTTTGTTGATTGGTGGAAATTACATATCTAAGCAAATTCCACGCGGACGCGGTGGTTGTTAAACCTGAAGCCAGCCCGCCGCACCACACTATTGCTCTGATGTCATGTGTATTATCTCCCCATGGGTTAATAACACCGCCGTAGGTTAAAATTCCGTTATCACTTGAATCTCCGCTAGTACCTGTTACACGAGTTCCTGCCGCTGTGACTACAGAACCGAGAACACTTCTATTTCCCCAAGTGTTTCCTGAACCTGTGAAATTCTCGATATACGCAACGCTGGCATTAACGGCATTAACTGCAATGAATTTGTTGGAAAAATTACATGACGTTGCTCTAATATTGCTTAAATTCACATCTAAACCGGCACCTGTTCCTGCGGCGACAGTACTGTTTATATTATTGATCAAGGCACCGACGCTTGATATTACTGAAACAGCATTAGTACCACTAGGGGGCAAACAGTTGAACCCATTTACTGTAACAAAACATGAGTTGCTGTACATTTTAATTGCATCTACCGTTCTGCTCGTAGATACAACACTGTCACCCATCACAGCTATTTGACCAGATCCTGAATATCCAGATAGACTAATAATCTCTGCATACGTACCAGCCGCAACATTTACTGCCACAAAATGGTTGACGGTATCAGGAATCATACTAACTGCCTTTTGAATCGTCCTAAACGCCCCACCCGCCGTATTCGCCAATCCATTATTACCGTCGTTCCCATCCGTACGCACATAATAGGTAATATCCGCTGTCGTCTGCTGCGGGGTGGTCGCCAAAGGCGCTTTACTGTTGAGTTGTCCTTGTATCCCGCTGGTCACTCCATCCAAATACCCAAACTCCGCATTCGATACAACGCCAGTGCCGATCTTGGTTGCATCGATTGCCGCAGCCGCGTTAATATCCGCGTTTACAATAACCCCGGGAGCAATCGCGGTAACCCCATCCCCTGTGCTGGTCACATCCCCGGTATGATTGGGATGTACATATTTATTGGCTCCGGCCGCTACTCCGTCCAGCTTCGCCTTATCCGCTGCGGCCATCAGTCCGGCAGCGCTAGCAGTGGCTGCAGCTGTGGAAGCCTTAGCATTCCAAGCGGTGCGTTCCGCCGCTGTAATATGCTTTACCGTATCCACGGCATGATCCTGCACATTTTTAACGGCAGTATCCAAAACATCCATATTACCGTTCAAATCGGCGATATCGACTATATCTGTGCCATCCGGCTTTTTCAGCCCCAAATTGCCCGTAGTCTGCATAGTTCACACTCCTATTCGTATACTCTTAATTCATTCCATGTTCTGGCGTGCGCAGCATTCCAGGTGAGTGACTTCAGCGAATTCCACCAGGTATAGCTGTACACAAACTTATAATCCAGATGTGCAGGCTTAATCTCTTCTATGATTTGGATTAACCCTGCCATGTTCTCCGGGATGCCCAGCGTCCCTACAAAACGCACCTCAAAGCTGTATGCTCCCGGCACCTCCACAACCTGAACATCCCCTCCGGAAAAAGCGGACGCCGTCCGCCGGATCATCTCCGGCGTAGTGGTCCCGCTTCCGCGCAGCTTGGCCTTGATCATTTCCCGGCGGGCGGCATAGGATTTGGTATTGTCCGTGGTCAGGGCCAGCACCTTCTCCCAGCGCGCAAGCCCCCAGGTTGCCGACTCCACATTCGTCTGCAATGCTGAATCCTCTATCGAATAGGCCAGCTGTCCGCATTCCGCAGCATGGCTATCCTGGATCTGCTCCATCTCAAGTACACCCTGATAATACTCCGGCAGGTATTTCATCAGGTCAGGCTTGCTAAATTCCGGCCCGTCTTGTGTCGCGGGACTGGAAGAATAGCTTATGGTCCCGTATAAATTCTCGCCATAGGTCATAGTTACACCCCTTTAAGCTGATTCCAGCTCAGCGGGCCTTTAGGCATGTACTCATGCGTATGAGCCGCTGGCGGATACACCGCCGGCTTCCCGTCTACCCCTGACCAAGGTACGGTATCCGCCGCCTGCGCGTAATCCACTTTGCCGTTGTTGTTGGTGTCATAGATGCTTTTCAGCATATCACCGGTGCTTTGTGAGGCTACGAGCAGTTTGTTGACAGTGCCCGTACCGATGTAGAGCTTGCCTGTATCGGTGCAGAACCCGAGTTCGCCAACAGCAAGAGTTCCCAGTGCGCTTTCTTGGCCGCGGCGGATTTGAATTAAAGTCTTCAGAGCCATTATCATCGCCCCCTAGAATGTGCCGCCGTCAATAGCACCCACCATCAGCCGGTTGCCATTAACTGTGTCGTATACGATGCTGCTTCCATCTACATTGGCCGCTACACCGTTCGCATCGACGGTGATCCCTTTGCCGGCGGTCACTGCAATCGCATCGGCCGTCACACCAATCCCGTAGCCTGCCCCAATGTTCAGTGTTACTGAATCGGCTTGTCCGCCCCCGGTAAGGCCATTGCCGGCTGTAATCGTCTGTAATGCTCCACCCGTACGAACCCAGGCACTGCCGTTCCAGCTGTAGATTTTCTGCTCATCGTCAACATAAGCCGTCCAGCCCACAGCCGGTGTATAATACACCCATGCCGCAGATTGATACTCGGCAATTTGACTGGTTTTGCCCGCCCAGACGCCTGTTGCCGCCGCAGGAATAATGTAACGGTCGCCCTCCGCAGGACTCGCCGGGGGAACGGCCAGATTCTGGTCCTTCACTGAACTCTGCGGCTCGATGTTATGCTTGGCCAGCTCGATCTCATTCCTGATTTTTTGTGCTGACCACAGATCGGTAATAGCCGTTCCCGCATCATTGATTACACGGTGCTTGGACGCATCGTCGATATGGGTTTTGATCTCAGCTGCAGTTTTGATATTTGTACCGTCAGAGATCTTATTTATATGTCCTGCCGTGATGTCTGCCTTCAGTACCTTGGCATAGGTTGCCCCATCGGCAACCTCGTCCACTGACCCTGTCAGATCACTCAGCTTCTGCACATTGATCCGGCGCCAGGCCGCGCCATCGTCAAAATACAAATAGCCGCTGTTCGTTCCGCTGGTTACAATGTATACCCGCCCCGCAGAAGCGGCTGCCGGACGTGAAGCCTCCGGACCGGACATCGCCCGGCCCACCATGGAGTTGGAGGTGCCGTCACCAATATAGACTTCCTTGGTATCTGTGCAGAAGCCCATCTCGCCCGCCTGCAGAACTCCATAAGCAGCAAGCTCCGCCCGGGTGCCGCGTTTTACTTGAATGGTTTGTGCCATTTTACACCTCTCTTCTAAAAGATCCTCCGTCTATGCGTCCCGTTGCCTTGTAGCGTTCAAGCTCCCTTTGGGCAGCAGTCAGCCCCCACTGCAGGACATTGATGTCATCGGCTTCCACAGTATCGCCCGGTGTCTCATAAGTGACATAGACTTCAGGAACCTCGGCAAAAATCTTAATCATCCTCCGCCAAGGCGTTTCATCCGGAAAAGAAACTGAGAAATTCCGCAGCTCCACTCCGCTGTAACGGGAACCTGTGTACACCGCAATGCTCTGGTTGTTAATGTTGTCATGTGCGAGCAGACCGCTGTAAACCCCATCTGTAAGGAACAGTTTCTCCTCAACAACATAGCTGCCGCCGTTTGCTTTTTTGTTCAGCTTGTCCGTAAATTCATCAATCTGCTGCGGGTATCCCATCACCCTACACCTCCAGCACGACGCTGCTGAACAGCGGCACTTCAGTTTCGCTTAGAGTGACATTGCCCGTTACGCCGTTCAACTTCAGCCCGCTATAGTCCACAACGCCTTCTGTATCCAGCAGCAGTGAACCTATTACAGATTGGCTGATATAGGACGCAGTAAAGGCCTTTTCCTTGCGGTATTTCTCCAGGATCTCCTTAAAAGCATCGATTACCTCCTGCAGACTATAACCGGAAGCAAGTGTAACCTTGGCGCTCACGCTGATGCTTTTCCCGGCTGCAGCCGCCACAGTCACTACCGCACCCACCGGCGCTTGGCCTTCACCCTGTCCAGAGACAGGATCGATATATTGCTGCACCTGCGACACCAGCAGTTCTGAGGCAGGCCGCTTCGCGGCATCCACAATGACCACTTTCACCGTCTTCGGTCCATTCCATAACGGAAAAACCCGCGCTCCCCCTACGCCGTCTATTTGCAGCGCCCATTCCATATAATGATATTTGTTGCCGCTCGTTGACGGGCGTCTGACCGACTCCAGATAACGCTGGCGCAGCGCCTCGTCATCCTCGGCATTTTCACCGGGAATCAGCAGGGCTGTTATCTCTCCGCGTGCCAGAACAGGAATATAATCAATAGGCAGCAAGGAGCCAAAATACCGGTTGCCTTCCTCCCCCGCTGTTTCGCTCTCCAGCCTGTAGGTTCCCGGAGCCAGCTTCTCCACCGCCGTATAATGCAGCAAATCGAGCGAAAAACGGCTGCCCAGCGGAACATCCAGCAGTCCACTCGCGCTATTATAGAACATTGCTTTGAGCTCGGCCTTGCTTGCGGCACGTCTGGTTATTCCCGACCAGGCAATGCTGCGTTCCAAATATTCACCAGTAGCCGTATCCGCGAAAAACAGATTGCTGTTTACATCCAGCTCAATATACATCTGAGCCATTTCGGCGGCCGCCGGAGCCAGCGCATCATAAATGATGCTGCCTTCACGTTTATCCAGGCTGGATGGCACACGGTCCAGCATCCGCCCAAGCAGAGCCTCGAACGTCTGATCTTCATACACCCTCACTCATCTCCTTTCTTAGCTCGAAATTTCCGTACTGGGTAATCACCTTGCAGCTAAAGCTCAGATTATCTCCGTTAAAAGAAACCTTAGTGTCCTCCAGCCCGATAATCCGCTCATCCTGAAGCAATGCTTCACTAACAATACGCCTGATTTCAGCTCTCACCAGCAGCCTGTCTTTTCCCAGCACAAGACTCCACTCAGTCCCGTAATCAGAACTGTAGATCAGATGCTCATAACGGTCTGTCCGCAGCATTTTGGCCACTGCCTGCTGCACTGCTTCAAGGCCGTCCAACCGGCTCGTAATTCGTTTTTTGTCCCAATCCATTCTGTAGGTCAGACTGGACATTTCAGTGTTCCCCAAGGAGGTGTCTCCTTCAAGAGGTGCGGTGATCGGGCCTGCATTTCCAATTACGGGTATCATATCGGATCCACCAGCCTGTCCAGTACAACGTAACTCTGCCCGCCCTGCATCCGGACCATCAGGACACGGTCCCCCTTCTCAAGCCCCCGGCGCAGAACAATTTCCCTTCCATCCCATTCGAGCTTGCTCTCCATGACGGATTCGGGAAGAACCAGAGCGGCTCCTGACAAAATAAACCGCTGGTCCACCTGAATCTGCAGCGGTGCTGCCACGGTTACCGTCCCATACGAAAAAGCCACAGGGTTGGTACTCCCTACGGCGCCGAGACTTGCTTTTTTTATAATATCGAGCATTATTTCTACACCACCTTTATATCCAGGGACATGGTATGCTCCCCGCCAGAAATCTTATGGCTGCATTGCTCCACCAAAAACAGTCTGGTGTCCAGCGCATCCAACAGCACATAAATCAGGTTGCCTGCACGAACCCGCAGATCGCCTATGGCCTGTACGGAAAGACTTGTTTTTTCCCGGTTATGCAGCTTCAGCAGGTTGTCTGCGTTCTCTTGAATCTGTGCGGCGTTCGCCTTGTCATCGGCTTTTTTGTAGAGATGCAGAATACCCCAGCGTTTCACATTCTCCGGGTCGCTGACCGGGTAGAACTCCCGCTTGCCGCTCTCTTTGTTGTCCTTATAGAGATAGATCGTATTGTAGGTATCGTCATCAATGCTTTTTTTGAGCGAATAGTCATAAAGATAATGTCCTGCTCCCAGCACCAGATCAAGCTTCATCGAGTCCATTCCCCGCAGCGTCAGCTGGCCGAAGTCATCATAAAAAGCCATTAGCCGCCCCTTCTTCTCCAGCTCACCGCCAATAGCCCTCATAATAATATCCAGCAGCTTCTTATCATCTTCTATTAAAGAAGGCATGCGGTATGTGGTTTCTTCAAGCACTCCGGTCTTCAATCCGTAGTCCTTGGCAATTTTTGAAATGAGCTCACTGGCTGTAACATCCTGAAGCACGTAGCTTCCGTTGCCGAGCAGATAGCGGATCTGGTCATAGGCCGTCAGCTTGATCTGCTGATCACTCCCGGTATCAATGCTGAACACGAACCCGTAGAATACATTGATGCCATCTTTGCGGAACTGGACAATATCCCCGTTGCTGATCTTAAATTTGGGGTGCTGATAGATGCCGCTGTCGATAATAGTCATGTCCAGCGTTGCCGGCTTGCCTGCCCGGGACGTCTTCCAGGAAAGATCTGAGACAATCCCGGCAATATCCCACAGGAGCCCTTCTTTATTTTTCAACAGCAGTTCCATACGCTTTCCCTCCTACGGCAGCTTAAGGACTTTGCCGATGGGGAGCTTTTTCAGCTCACTGTCCTTGATGCCGTTAAGCTTCTGTATCACCTTATATTTCTGACCATCACCGAGAATCTTCTTGGCAATGCTCCACAGACTGTCGCCCGCTTTCATCGTGTACGTTTTGGGGACCGCTTTATCACTCGCCCGCTTTGGCTCTGCCTTAACTTGGCCCTTGACGATCTTTACAGGACTGGCCTGGTAGAACACGTACTTTTTGAGGGATAGTGAATACTCCACGTCACCGGAGGTGCCCGCGCTAAGCTTCCAAGTAAAGCTCTCGATACTCATGGCCATATTCAAGGCCAAATCATTCGGTACGGCTGAGTGATCCTGCTCCCCCTTCAAGTTCACCCCGGACAACACAAACCGGATCGGCCTGCGGCTCTTCATCCATTTCTGGATCATCTCCACATATTCAAAAGGCCGCAGCAGCCGGTTAGGCCCCTCACTGCGCACCAGCACAAAAGGATAATGCTGCGCCGGGAAGATACTCTCAATCGTGATCTCCGTCAGCTTCGGGTAGGCAATGGCATTGATTTCACCCAGATCGACTATGGTATAGCTTTTGCTGTCTCCCGACTCTTTGATTTCCAGCGTCTCCGGATTCACAGGCAACCGGAAGAGATCCTCCAGCTCATTAAAACTCAAGAAAAAACCGTATTCTTCCACGTTACGTATACACCCCCTGGGCCGTAGAGACAAATTCCTCATTCAGCTTTTGCCCGATCTTGTTGATGATCGTATCGATGTCACCGGCATTGTTGATGTTCCCGGTAGTCACCTGCACTGTAGGCGTCAGCTCCACAAAGTTCTGAATGGCCTGAATCTCCGCCAGCTCGCGCATCATTTCAAGATCCTCACTGGAGATGTCTACGGTGTCGTTGATGGAGCCGACCTCATTTACCCTGTTCACATTGTTCAGGTTGCCGCCCTGATTGGCAAAAAGACCGGCAGTGTTCTGAATCTGTTGCCCGCTTGCTGGCGGTTTTGTTAATTTCTTGGCATCGCGCCCTTTATCAGAAAATGCACTCGAAATACTTTCGACCTTGTTGTCTGTCCATTCTTTAGCCTGTGTATAGCTGGAGTTAAAAGCATCTTTCGTATCCACATACTCTTTATGCTTCGTTTCCTGCTTAGTGATATCCTCAGGAGGCTCCAGTGTTTTGAATTCTTTACGGTACTTATCCACCAGCTCGCTGGCGGCATGGGGAACCTTCAGCCCATCCAGGTCAAGCTTGATCGTGCCGATCCCCATCTTATCGAAGAAAGGAATTTTGCTTAACGCTTCAGCCATGCCGTTGAACTTGTCAACCACCCAACGGATCGCCTCTACCATAACCTTCACAAAACCATCAGCAAAGCTCTCAACACCAACCGCCATATTATAGAGGACATCCAGCGTACCCATACCTAAGCCATATAACAATTGCTTCACAAAAAGAACAGCAGTATTAAATCCATTAACAATGCCATCCCAAACCACATAAAATCCATTTTGCAGGCCTATCCAAATATTTTGGAAAACCGCCATCAACCAGCTGAACGCCCCCGCGATAGCCCCTACAACCTGCCCCGCCGATATCCCCAGGTTCTGAAAAATTAAGATCAGACCCGCGATTACCGCAATCACGATTAGAATCGGCCAGTTCGCAGCCAGCCAGGCTGCAGCAAGCAAATATACCTGAACGATCATTGCCGCCAGATAGACAACCGCTATCGCGATAAGAATCGGCTCAATAATCGCCCAATTCTCCTGCACTACACCAACCAGCCATAATAATCCATCCACAATCATCCCGATTACATTGGCTATCACCAAAAAGCCATTTGCCAATGCGTCAATCGTTGGGGCCAGTTGGCCGGAGGTGAGCGCTTGATTCAGTGTATCCATTACAGGCCGCAGGGCCCCCAGCGCCTTTACACCGATTTTGCCCATTGCCGCATCCACATTATCATTCAGCTTGTTCCAGTCTGCAATATCTCCTGGTTTTACAGCAGCCTTGACTGCCTTCTCCCCGAAAGACTTAATCTTGTTGAACGGGGTAACCCAGTCCGCAGTCTTCAAAAAATTCAGTATCTTGGAATCTGGCTGTGGCGGCGTTGGAGGGACCGGTGGAACCGGAGGCTCTTTTTTCAAATTGATCTTGGGTGTAGGTAAGGGTTCAACTTTAATTTCAGGCTTCTTTTCTTCTTCCTTTTCCTCCTTTTTTTCTTTCTTTTCGAACCCTTTCCACCATTCCACCTCTTTGGCCTTTTCTTCTTCCTTCTTAGCCGCCTGTACGGTTGGAGAAGCATTCAGCATACGCACCCCAAGCTGCTGGGACTGACTGGCCTGCTGACTTTGTCCGACAACAATGTCTCTGGTGACCAGAATCTGCGGCGGCATTCGCTTGAAGCCTTCCAGCAGCGTATCATTAATATCCAGCAAAGATTGGTTAACTTTGTCCAAAGTGCGGTTTAATTCATCGCTGGAGCGTGTAAGTGCGGCTTGCATTCCCTTAATCGAACGATTGGCAAGATCCAGCTTGACACCAATGCGCTGGGACTGTTTATTTAACACTTTCCAGATCGCAAGCGACTTGACCGGAAGCATCACGGCTTTAGAAACATCTATTCTCATTCTTCCACCCCCTTCATCGCCTATCTCCTCTTCCCCTTGCTCCGCGACTGCTCCCGCTTCTCCTTCTCCACCCGGACAGCGATCATCGCATAGATGGCAGCCCGTTCGCGTGCGGACAGCTTCATCAGTTCATGCGGTAAAATATGCAGCTCATGGAGGGCGTAGTAGGCCAGGTTGGCCTCACCGTCGCCTCCGTTAATTAGTTTTTTACTTCTTCCACCAATTCGTTCATATCGGTGGCGAAGCCGTTGAGCGCCTGAACCCGTTCACCAAGCGCAGCGAATTCGCCGGGCAGCAGCATTTTACGCAGCAAGGCCTCTGCACCAAGCACATTATAGGAACGCTGCAGTTCCGCATTTTTCAGATCGGGGTGCACTACGCTCGAAGTCATCAACTTGGCCATGTAGTCATTGGGATCAATCTCAGAGGTATACACCCCACTTTTCCCTTTAACCTTGCGGGTAGCCGCCTTGCGGCATTCCTGGTTCTCATCCTCGGTCATGCTGCGCAGCTTCCAGGCCACGGGTTGGCCCTCTTTATCCTTAAAGCGCTGGGAAACCACAAATTCCTCCGTTGTATCACAAGCCACATTTTGCGCAAAAAACATACTTAATTCACTCATGATGATCCTCCTATAAGTTTATGGGTTTAAGTTTTACCGTACAGACAGAGAAGAGACCCGCCGCCTGCCGCGTCCGGGCCGTTCTTCCTCAGATCTGTATTTCTCTTATTACTGAAGTGCAGGGCTGCCAAAGGCCTGGGCAATCTGTACATCCTCAAAGGTAAAGCTGACTTCTTCCTCCAGAGCATCCGACTCCGTATCCAGTGAAGCCATAATCACGCTGTCCAGGTTAACACCTTTCAGAATGATCCGCTGTGCCCCGACACTCGATGAAGGATCATCATTGGTAACCTCGATATCGAAGTACTGATCCACACCTGTATGCATGTAGTCAAGCATCATTTGACGGAAACGGCTGGTCATATAAAAAATCGTCATCGTGCCGCTGCCCGACCATCCGGTCGCTTTATGCTGCACCCCCCGGCGTCCAAGTGTTTTCACTTCCGCTTTTGTTTTCTCTACGGTAGCTTCAAGTGTTTTTACATAGAACATCTCTTCTGTTTGTGTGCCAATCACAGCATAAGCCCGGCCTTCCTGGCCGGAAAGAGTATCGCTAGCCTTCAAAAATGCCATCTTAGACCACCTTCACTTTCATATATACTTTTTCTACGGAATCGACCGGTTTTACAGCCACATCCACAACGATGCTGTCACTGTCCGTACCGGCAGCAACCACAACATCCGTCTGGGCCTTAAAATCTTCAATCGCCCCGATATTCTGCAGATCATTCATATAAGTCGCACATTGCGACCAGAACATTGTCCGGCCATCTTCATTATTGGCAACCTTGCCAATGTAGTACTTTTCAAAGATAGACTTCAGATCATTTGCAATTCCATCCAGCACACGGAGTACACGGTTTTTGGAGAAGGCTCTGCCTTTATCCGGAGCATATGCCGTAAAAGTGTTGATATCCTGCTCTACCACAGCCCGGCCGCCGCTGTAAGTGAAGAGGAATTCACCGTTCAGCAGGGCATCTGTTGTCTCAGAATGGCTGAGGCGCACATCGGCGTCTACGGCATCATCATAGGCTTGATAAGTTAGAGACTCGTTTACGGCAGCAGCAGCCGAGGCACCGGCTACCCAGGCAACCGCATGCTCACCATCAATTGTAGTCCCATCGCTGAGTACTACCCCATTTTTCACACTAATAATGCCCTCATGGCCGGCAGCAGCATAATCAGACACTACAGCCTGTACCTTTTTGCCTTCCATATCCCGGAGCCGTTTCACAAAAGCGCTATACAGCGCCTTCAGTGAATTGTCCTTGGACAGCAGCCCGACGGTCTGAAACTCTTGAACTTCAAGGGCACCCAGGAAATCACTATGCGCAGCGTTCGTTACTGTACCGCCCGCTCCACCCGCAAGACGTATACCTGCCGTCAGGGTCAAGCCCTCAGTCCCGTTCTTCTGGAACGTAACATAATCGTTAGCTGCGAGTTCATCGGCGTCGCCGACAGTTTGTTTGTCCAGCTCTGTTCCAGCCAAGAGTGTTTTTACATCGAACAAAACATTATTTTCAATATTTTTTTCAATGATTACAGAGATATCATTCCCGCGCTCGCCGCCGTACTTGGCCGTAACCTGCAGACCATTATTCGTTACCGTTGCTTTCACGCCTTCATTCAATCGGTATAGCAGCACAGTGCTGGCCCGCTTCAGTGCTTCACGTACCGGCAGCAGGGTGGGATGTCCCAAATCGTAGCCAAGCAGCTTTTCAAAATCCTCCTGGGCCGTAATCTTTGTAATGACTCCCGGTGCTCCCCACGAAAGAGAAAGCGCGAGCGCTGTAATGCCGCGTGTCCCCATTTTTCCAATTGCACTCTGATTTGATGCTACATTCACGTACACCCCAGGGCGCACCTTATTTTGCGTTGTCCATGTTCCACCAGCCATTAGATAACCTCCTTATTTAAAAAGCTCTTCAGTTGCTCTCTTGCTTCTTCCAGCGTGTAGCTCTGATCCTCCAGCAAAATAACATTCAACACATCTTTTTCCCCCGGGGAAAAGTGCAGCGAGTTTACAATCTGCTTTGTGCTGAAGGCTGTATCACTAACTTCATTTGTATTCATTTCAGCCTTTCTCCTCCCGTCATATGCCTCATAGGCACCCTCTCCACTGCTGCAGTTTGCAGATAGATCATGAAATCAGCCGTAAACAACGGCCCTTTCCCTTCTGTGCCTGCCTCCCAAGCCTGTCTGATTACGCGAAAAGCCTCGCCTTCACGCTCCATTGAAGCCAAAGCTTCACTTAATCCATCAGCCATATTCTCCGCATTTAAGCGGCTGCCTTGTTCATAACGGATACCAAAACGATAGACCGCCAGATATCTGCCTTCCCGCTGCCTGTCCAGAGTTGCCGAGATTAATCCAGGCTCAAAATAAGCACCCCGCGGCTTTTCCCCGCTGACATATACCGGTAAGTCCGGAAAGTAGCGGCCAAGAGCAGCGTTGATCTGATTCCGTAATTGTTGTACAGACATATTAAGCATCCTTTCCTGACCCTGCTGGCACGGTCACCCGATGCCATTTACCTTTAAGTCCATTAATAATTAGCCCTGTATCCCCCCTTAAATTAAAAACGGATATATCCCCCTCTGCAGGAGTAATATCCGCTTTGTATTGTGGCAGGTGCCAGAAGAAGCTTTCACCGCAAAAAATCAATCATTCGTTTTTTAACGAGGCTGAATCCTCGGAGCATTCATGCTCCTGCGGTGTCCTTCTGCTTTATTTGCCATGCTAACATCATACCCCCTTTATTTCCGCATGGAGCCGGTATTAGGACGAGATTAGAGAGAACATTGAGAGGATTCCGGGCGGTTTTTAGGCGGTGATAACTTAAGTCCCTTTCGGTGGCGGCCAAGGGTATCTACCTCCCCAACAAAAAAGCTGCATCATCCCCTCGGACAATACAGCCTTCGCTTTTTATTTTGAACTTCAGTGTTCTATTTATTTTACCCTCCGCTTCCTTAATATACGCTGGGCAGTCTCCTGCTCTTCAGCTCCTCTTGCTTCATGGATGATCCGTTTTTCATTAGTGAATCGAGCGATAACAACCCCAGGTCCGTCAGCGCAAGCGCCATCTTGTAGAATGCCTTTGACCGTATTTTAACATAGGTATCCTTGCTGACCGGCGGATCAAACACATGATTGTACACGGTGTAATCATATACCTCATCTCTACGCATATAGCGTTCCCGCACGAGCTGCTGCTCCCGCTTGTCCAGCCTGTCCACTACAGAATCCAATGCAGCACAGTAGGCTCTTCTTGCGGCAGGAACATCTACGTTATGAGCGGCGATGGTCGCAGTCTGGTCAGTAATGGTATGGGTCGGACCGTGAAATCTCTCGGAGTAAGAATACGTTATCCCCGCTTCCTTCGCTTCAAAAGTAACCGTCTTAAAAATACGGTACTTCTCCAACATGCTCTCTATAGTGGTTTGAGTACGGCGGCGGTCCAGTTCAGGTAAAGAAGATAAATTCATCATCATATATACACTCCTTTGCATTTGGGCTGGTTTCGGATGATTATTGCAGAAGTTTCCTGTGAGATGTGGTAAAATTCTTCTTGTTCGTATATTGTTCGCCTTTTTCAATAATATACCACCTGATTACCAATTCCGTAAAATCCCATATAAGGCCGTTTGGAAGGAGAAATTAGCTATTATCACGATTTATCTTAGATAAACGACTTGTATTACCTTTTGGCATAATTGTTCACTTTATGTTTACCTATTGACAATAATAGCTTATATTATTATTAATAGAGCAATAGGCGATAAGGAGTGATCAACGATGGCAGAAGAATTCGGCAATTATCTGAGACAGCTTCGGGAACAAAAAGGGCTGACAATCAATCAACTGGCCTCTCTTGCGGGCATCAGCGGTGCGCAGATCTCCCGGATCGAAAACGGACGGAGAGGGGTGCCGAAACCAGCTACCTTGCGCAAGATCGCAGAGGCTGCTGATGTCCCCTATGAGGAGCTAATGGAACATGCAGGCTATTTATCCGAGGATATGCAGAGCGGTGCTGAGGATAAGGTTCCCGAATGGGCCACAAGTAAGGATAAGCGGGATTTCCGCAAAATGCTGGAGGATGACGGGGAGCTTATGTTTGACGGGATTCCCTTGAATAAAGAAGACAAACAGCGGATTAAAGATGTGCTGACCGGCCTTTTCTGGGATGCCAAGCAGATGAACAAAAGAACTATACCCAAGCACGATTCAAGCGGCGGCAAGAGTTGAATAACATCACATACATTATTATGCGCGGGTGAAGAATATGGATGAGATCATCAATAAGTTGATCAAAAAATATAAAACGAACAGCCCCTTCGAGCTCTCCAAAGCACTGGGCATTCATATTCGGTTCATGAACCTTGGACAGAGTACGAAAGGCTTGTATTACCGGAAGCTTAGACGAAGATTTATCGTGATTCATAATGAGCTTCCTTTGGAGTGGCAGCGTTTTGTTTGTGCGCATGAGCTCGGCCATGACCGCCTGCATAAAGGAATCAACCGGTTCTTTCTGGAGGAAAATTCTTATTTTTCACCTGGCAAGCTGGAACGCCAAGCTAATTTATTTGCCATCAAGCTTTTGTCATCGGGGAGTTCACCCGAACAAGAGGAGCCTTTATTGCGCTATTACCTGCGGATTGGCATCCCACCGGAAGTCATCTTTTTTTTAGATGAGTAGAGAACGTATGTTCCTCCACTCCACATGACAATCAGACTGAGATTCCGCTATTTGTCCTATCTCCCCTTATTTTAGGGCTCAAACGAACAATATAACGGCCCCTGAGTCCAAATCGGCCAGGAAAGCAGGCTTTTTCGCAAAATAAGGTCTCTGCTCAGTCCGCTTCATTCCACTGATAGCACGTAATCCTCCTACATCGTCTATATCATCTGAAGCTTCCAAGAACCCTCATGGTTTAGCATTACATAATTTCCGAACCCACAAGAAAAGGAAAGCATAATTTCCCAATACAAAAAAACTCTTACAAAAGTAAGAGTTCATTGTCAGCTCACAAGCTGAGTTATCGGGATGACACGATTTGAACATGCGACCCCCTGGTCCCAAACCAGGTGCTCTACCAAGCTGAGCTACATCCCGAAGCGTATAAAATTATGGAGCGGGTGATGGGAATCGAACCCACGCTATCAGCTTGGAAGGCTGAAGTTCTACCATTGAACTACACCCGCACAGGTGTAAAATCGGGATGACACGATTTGAACATGCGACCCCCTGGTCCCAAACCAGGTGCTCTACCAAGCTGAGCTACATCCCGTTAATATATTCCTCATAAATAAAAAATGGCGCGCCCTGAGAGATTCGAACTCCCGACCTTTTGATTCGTAGTCAAACGCTCTATCCAGCTGAGCTAAGGGCGCAAAATCAAAATTATGGAGCGGACGACGGGAATCGAACCCGCGACCCTCGCCTTGGCAAGGCGATGCTCTACCGCTGAGCCACGTCCGCAAATAAATGGTGCGCGTGAAGGGACTTGAACCCCCACGTCGTAAGACGCCAGATCCTAAGTCTGGTGCGTCTGCCATTCCGCCACACGCGCATGATACTGATAAAAGTGAGCCATGAAGGACTCGAACCTTCGACACCCTGATTAAAAGTCAGGTGCTCTACCAACTGAGCTAATGGCTCCCATTTGGCAGGGGATATAGGATTCGAACCTATGATGACGGAGTCAGAGTCCGTTGCCTTACCGCTTGGCTAATCCCCTATGATGGATACCTATAGTATGCCCACAATCACTTTCAATATGAGAACGATTATGGTGGAGGCTGAGGGGTTCGAACCCCCGACCCTCTGCTTGTAAGGCAGATGCTCTCCCAGCTGAGCTAAGCCTCCATATGTATGGTTGTCCTCAAGGGAAAATAATTGGTGACCTGTATGGGATACTCTCCACTCCGTTACGAGATTGCGAAGTATTCCTTACGAAGCCGGTGCTTCAACGAACCCCATGGATTCTCATCCCAGAATTCGAAGATGTAAATTGGTGACCCGTATGGGATTCGAACCCATGTTACCTCCGTGAAAGGGAGGTGTCTTAACCCCTTGACCAACGGGCCGCAAAAATTTGTGGAGCTCTCAACCGGATTCGAACCGGTGACCTCTTCCTTACCATGGAAGCACTCTACCTACTGAGCTATGAGAGCATGGCTCCCCGAACAGGACTCGAACCTGTGACAACTCGATTAACAGTCGAGTGCTCTACCAACTGAGCTATCAGGGAATATATGCTTGGCGGCGTCCTACTCTCCCAGGACCCTTCGGTCCAAGTACCATCGGCGCTGGAGGGCTTAACGGTCGTGTTCGGGATGGGTACGCGTGGAACCCCTCCGCTATCGCCACCAAACGGGCACTTGCGGTGCAAATGCTTCAGGAATTTGATCGCCTGAAAACTGAATCCGAAACGAAAACTGCATTTTAGTTATTTGGATAAGCCCTCGACCGATTAGTATTGGTCAGCTCCACACGTTGCCGTGCTTCCACCTCCAACCTATCTACCTCGTCGTCTTCAAGGGGTCTTACATGCTGGGAAATCTCATCTTGAGGGGGGCTTCACGCTTAGATGCTTTCAGCGCTTATCCCGTCCGTACGTAGCTACCCAGCCATGCTCCTGGCGGAACAACTGGTGCACCAGCGGTACGTCCATCCCGGTCCTCTCGTACTAAGGACAGCTCCTCTCAAATTTCCTGCGCCCACGACAGATAGGGACCGAACTGTCTCACGACGTTCTGAACCCAGCTCGCGTACCGCTTTAATGGGCGAACAGCCCAACCCTTGGGACCTACTTCAGCCCCAGGATGCGATGAGCCGACATCGAGGTGCCAAACCTCCCCGTCGATGTGGACTCTTGGGGGAGATAAGCCTGTTATCCCCAGGGTAGCTTTTATCCGTTGAGCGATGGCCCTTCCATGCGGTACCACCGGATCACTAAGTCCGACTTTCGTCCCTGCTCGACTTGTGGGTCTCGCAGTCAAGCTCCCTTCTGCCTTTGCACTCTTCGAATGATTTCCAACCATTCTGAGGGAACCTTTGAACGCCTCCGTTACTCTTTAGGAGGCGACCGCCCCAGTCAAACTGCCCGCCTGACACGGTCCCCGTACCCGCTTAGGGTACCAGGTTAGAACCTAGATACGATCAGGGTGGTATCCCAACGGCGCCTCCACCGAAGCTTGCGCTCCGGCTTCTACGGCTCCCACCTATCCTGTACAGATCGTACCCAAATTCAATATCAAGCTGCAGTAAAGCTCCATGGGGTCTTTCCGTCTTGTCGCGGGTAACCTGCATCTTCACAGGTATTAAAATTTCACCGGATCTCTCGTTGAGACAGCGCCCAAGTCGTTACGCCATTCGTGCGGGTCAGAATTTACCTGACAAGGAATTTCGCTACCTTAGGACCGTTATAGTTACGGCCGCCGTTTACTGGGGCTTCGGTTCACAGCTTCGGAGTTGCCTCCTAACCGCTCCCCTTAACCTTCCAGCACCGGGCAGGCGTCAGCCCGTATACTTCGCCTTGCGGCTTCGCACAGACCTGTGTTTTTGCTAAACAGTCGCTTGGGCCTTTTCACTGCGGCCCCCTCGGGCTATTCACCCTACCGAGGCACCCCTTCTCCCGAAGTTACGGGGTCATTTTGCCGAGTTCCTTAACGAGAGTTCTTCCGCGCGCCTTAGAATTCTCTTCTCGCCTACCTGTGTCGGTTTGCGGTACGGGCACCTTCTCCTGGCTAGAGGCTTTTCTTGGCAGTGTGAGATCATGACCTTCGCTACTGTAATTTTCGCTCCCCATCACAGCCCAGCCTTACGGTGTGCGGATTTGCCTACACACCAGCCTCACTGCTTGGACGGACATCCATCAGTCCGCGTCACTACCCTCCTGCGTCACCCCATCGCTCATAGCGGATTACGGTGGTACAGTAATTTCAAACTGTTGTCCTTCGACTACGCCTGTCGGCCTCGCCTTAGGTCCCGACTTACCCTGAGCGGACGAGCCTTCCTCAGGAAACCTTGGGCTTTCGGCGGATCAGATTCTCACTGATCTTTTCGTTACTCATACCGGCATTCTCACTTGTGTAATGTCCAGCTGTCCTTCCGGTCAACCTTCAACCCTTACACAACGCTCCCCTACCCCTGATGCAAAGCATCAAGCCATAGCTTCGGTGGTGTGTTTAGCCCCGTTACATTTTCGGCGCAGAGTCACTCGACCAGTGAGCTATTACGCACTCTTTCAATGGTGGCTGCTTCTAAGCCAACATCCTGGTTGTCTGTGCAACTCCACATCCTTTCCCACTTAACACACACTTGGGGACCTTAGCTGATGGTCTGGGCTGTTTCCCTTTTGACAATGGATCTTAGCACTCACTGTCTGACTCCCGGCAAGAAGTCCATGGCATTCGGAGTTTGACTGAGCTTGGTAACCCTTGCGGGCCCCGCACCCAATCAGTGCTCTACCTCCACGACTCCATTCACCGAGGCTAGCCCTAAAGCTATTTCGGGGAGAACCAGCTATCTCCGAGTTCGATTGGAATTTCTCCGCTACCCCCACCTCATCCCCGCACTTTTCAACGTACGTGGGTTCGGGCCTCCAGTGCGTGTTACCGCACCTTCACCCTGGACAGGGGTAGATCACACGGTTTCGGGTCTACGTCCACATACTCAATCGCCCTATTCAGACTCGCTTTCGCTGCGGCTCCGGCTTCTCACCTTAACCTTGCATGTTAAACGTAACTCGCCGGTTCATTCTACAAAAGGCACGCCATCACCCCTAAAATGGGCTCTGACTTTTTGTAAGCACACGGTTTCAGGTTCTCTTTCACTCCCCTTCCGGGGTGCTTTTCACCTTTCCCTCACGGTACTGTTTCACTATCGGTCGCCAGGTAGTATTTAGCCTTAGCAGATGGTCCTGCCGGATTCATACGGGGTTTCACGTGCCCCGCACTACTCGGGATCCGTCTCGGAGAGAAAGCTATTTGAGCTACAGGGCTTTTACCTCTATCGCGGGCCTTTCCAGACCTCTTCGCCTATAACTTTCCTTTGTAACTCCATGTGAGACGTCCCACAACCCCAAGGAGCAAGCTCCTTGGTTTAGGCTGTTCCGCGTTCGCTCGCCGCTACTGACGGAATCACTATTGTTTTCTCTTCCTCAGGGTACTTAGATGTTTCAGTTCCCCTGGTCTGCCTCTTCACACCCTATGGATTCAGATGTGAGTGACTGCGAATTACCACAGCCGGGTTTCCCCATTCGGACACCCCCGGATCAAAGCTTGCTTACAGCTCCCCGAGGCAGTTTCGTTGTTCGCCACGTCCTTCGTCGGCTCCTGGCGCCTAGGCATCCTCCGTGTGCTCTTATTAGCTTAACCATCGCGTAGATCGTTTCGCTTGTTCGCTCCGCTTGGACTCCGATCCTGTTCATGATTTACATCATTCACAAAGGGATCTCCGCCCAAAAGTCGCTGGACAATCGAAAATCTTCGCTTTCAGCATACTAATAACTATTTAAAACTTGTTCACACAAGTTTTAGCTAAAAGATGTTCTAAAACGCATTTTCGTTTCGGTATCCAGTTTTCAAGGATCAAGTTCTTGCATATACTTTTTGAAACAAGTTTGGTGGAGCCAAGCGGGATCGAACCGCTGACCTCCTGCTTGCAAGGCAGGCGCTCTCCCAGCTGAGCTATGGCCCCATACATTCACCCCAAAAAGTGAGGTGCAGCTTCGAGGTTGATTCCGAGTACTTTTCGGGGACCCCTACTTACTTATGTTGTTATATGGTGGGCCTTGGTGGACTCGAACCACCGACCTCACCCTTATCAGAGGTGCGCTCTAACCAACTGAGCTAAAAGCCCATATAACATATATAACATAAGGAAATCAATCAAAGGATTGATTGTCCGCTTGGCGGCGTCCTACTCTCCCAGGACCCTTCGGTCCAAGTACCATCGGCGCTGGAGGGCTTAACGGTCGTGTTCGGGATGGGTACGTGTGGAACCCCTCCGCTATCGCCACCAAACGTATACGAAAGAGACTTGCTCTTTCAAAACTGAACACGAGTGAGTGTTCGAACCCGAGGGTTCTAATGGAAGCTTACACTTCCGATTTGAATGTTCTCATTGCAGAGAACAATTCTCCATAGAAAGGAGGTGATCCAGCCGCACCTTCCGATACGGCTACCTTGTTACGACTTCACCCCAATCATCTACCCCACCTTCGGCGGCTGGCCCCCTTGCGGGTTACCCCACCGACTTCGGGTGTTGTAAACTCTCGTGGTGTGACGGGCGGTGTGTACAAGACCCGGGAACGTATTCACCGCGGCATGCTGATCCGCGATTACTAGCAATTCCGACTTCATGCAGGCGAGTTGCAGCCTGCAATCCGAACTGAGACCGGCTTTGCTGGGATTGGCTCCACCTCGCGGCTTCGCTTCCCGTTGTACCGGCCATTGTAGTACGTGTGTAGCCCAGGTCATAAGGGGCATGATGATTTGACGTCATCCCCACCTTCCTCCGGTTTGTCACCGGCAGTCACTCTAGAGTGCCCAGCCTTACCTGCTGGCAACTAAAGTCAAGGGTTGCGCTCGTTGCGGGACTTAACCCAACATCTCACGACACGAGCTGACGACAACCATGCACCACCTGTCTCAACTTTCCCCGAAGGGCACCTAATGCATCTCTGCTTCGTTAGTTGGATGTCAAGACCTGGTAAGGTTCTTCGCGTTGCTTCGAATTAAACCACATACTCCACTGCTTGTGCGGGTCCCCGTCAATTCCTTTGAGTTTCAGTCTTGCGACCGTACTCCCCAGGCGGAGTGCTTACTGTGTTAACTTCGGCACCAAGGGTATCGAAACCCCTAACACCTAGCACTCATCGTTTACGGCGTGGACTACCAGGGTATCTAATCCTGTTTGCTCCCCACGCTTTCGCGCCTCAGCGTCAGTTACAGCCCAGAAAGTCGCCTTCGCCACTGGTGTTCCTCCACATCTCTACGCATTTCACCGCTACACGTGGAATTCCACTTTCCTCTTCTGTACTCAAGCTGCCCAGTTTCCAGTGCGACCCCAGGTTGAGCCCAAGGTTTAAACACCAGACTTAAGCAGCCGCCTGCGCGCGCTTTACGCCCAATAATTCCGGACAACGCTTGCCCCCTACGTATTACCGCGGCTGCTGGCACGTAGTTAGCCGGGGCTTTCTTCTCAGGTACCGTCACTCCGGTAGCAGTTACTCTACCGGACGTTCTTCCCTGGCAACAGAGCTTTACGATCCGAAAACCTTCATCACTCACGCGGCGTTGCTCCGTCAGGCTTTCGCCCATTGCGGAAGATTCCCTACTGCTGCCTCCCGTAGGAGTCTGGGCCGTGTCTCAGTCCCAGTGTGGCCGTTCACCCTCTCAGGTCGGCTACGCATCGTCGCCTTGGTAGGCCGTTACCCCACCAACTAGCTAATGCGCCGCAGGCCCATCCTTTAGTAGCAGATTGCTCCGCCTTTCATCCCAAACCCAGGAGGGTCAAGGAATTATCCGGTATTAGCTACCGTTTCCGGTAGTTATCCCAGTCTAGAGGGTAGGTTGCCTACGTGTTACTCACCCGTCCGCCGCTAAGCTTACCCCGAAGGATAAACTCCGCTCGACTTGCATGTATTAGGCACGCCGCCAGCGTTCGTCCTGAGCCAGGATCAAACTCTCCAATTGGTATTGAAAAGAGCGATAGCTCATTTTGAAACATCTGACGAGAATTTGCATTCTCTGATGAAATTTCTAAAGCGTGAAACACGCTGTGAAACTCATCTGTTTTGGATTTCACTTGTGTGAAATCCCACTCACTCGTTGTTCAGTTTTCAAAGATCAATGTCTTTTTCTTTCATCGTCGCTTGTCAGCGGCGACCTTTATAATATATCACAGCGCCTATGCATTTGGCAAGCGTTTTTTTCGAAAAAAGTTTTTTTCATCTTTGCCTGCCATTTGCCGCTCTCCAAAACATTGAAAAGGAGCGCGAGATATAATGTATCACAGCGGCTCCCTTTTAGTCAACCTATTTAATTAAAATCAAAGGTTCTAATGTTTAGACTGGGAATAACGTCCTCCCCATGCATACTTGGACAGCTCCTTCTGCGGTGCAAACCGTGCATACATCCGAAATACAGTCTTATATCGATTGGCAATAGCATGCCTGATATTGTGGTCCAAGCGCTGATCACTTAAATCAAGGAGCATTTCATCAAGCTCTTTACGCAAAACATAGTCCAGCTCCTTGCATTCCTTCTCGTTGAACAACATTCCCAACATATGCTTGGCCTCCTTCATGAAATTAAGTCCAACAAAATCCGTAAGCGCCGTTGCTTGTGCAATTGAAGATAGTCCATTGGAGGGGAAGAGAGGGTTATATATCCACTTAAACTAGATTAACCGGAGCGTCGTGTCTGTAACCATAATTATAAAAAAATTCCTTATGGCTTTCTCCGAAAACCCCGCATGCGTTCCTCCCCGGCAAAACCCAAAATCGGATGCCTTTAATGTTATGCTCATTTCTGTGGAATTTTATGATAAAAGTGAAAATGTAATTGTGCTCTCAATGATGGCCGCTACGAATAACAGGATCACTATCCATATGGAGGCTCTTAAGGTTTGGCGCATAAAGGCCGGCCACGCCCCGCTTCTCTTTTCTCTTGCCGCAGCTGAACTGAATAGATCGGAGATTACATTCCAGCCAAACTGCAAACCAAAGGCACAGGCGATGATGATGGCCGGAATTTCAATAATCCCGTGGGGGAGCAGCCCTTTGACAATAAGGTCAAACAAATCCATGCCTTGCATGGCCGAGATATGAATCAGATAGCCGATTACGCCGCCATTAATCAATAAAAACAATGCAGGCAGGATACCAAAAATAGCACCCAGGAAGATTATGAGCACGCCTTTGATGCTGTTGTTCAGAAATATAAATTGAAAAAAGCTCCACTGCGGATGTGCGGATTCCTTGAGGCTGCCGCTGATTTTACTTAAACCCTCCAACTGGCCGGAAAGCAGCTTTTGCAGACTGCCGGTGCCAATCCAGCCTATAACTCCTCCCGCCACAAATAATAAAAGTGCGAACAATAAGGCCTTGCGGATGGTAGATAAATCTCTGGCGAAAGCGGGAAAAGATAGCATAATTACCTCCTGAAAGTATGTTGGACATATCTAAGGTCATAAGCGCCCTGTACGAGCATACATTTAGAACAAACAAGCATTTCGCATGGGAGAGGAGCGCTGACATTATGAATTCTTTTTATGTATTCAGCGGCAAAAAGATAAAACGGTTCATTTATATCTTTGCCGCTGCGCTTCTTGCTGCCGGTGTCGTCTATGTCGAGAGAGGGAATATTACCGTTTTTTCGGAAACGGCCCCTTCCGCCATTTACAGTGTGCCGACGGAAAAGAAGCTCATCGCCTTAACGTTTGACATCAGCTGGGGAGAGAAACGGCCCGGACCGATTCTGAAGGTGCTCGAAGATAAAAAGGTAGATAAAGCGACCTTCTTCCTCTCTTCCCCCTGGAGCAAGACGCATCAGGAAATCGTTACAAGCATTAAAGACGCAGGCTACGAAATCGGCAGCCACGGCCACAAGCATGTGAACTACAGTGCCTTAAGCAATGAAGAAATAAAAAACCAAATCACCACAGCCCATACTGTATTGACGGAGCTAACCGGGAAAGAGCCAAATTTGATCCGGATGCCGAATGGTGATTTTGACAAAAGAGTGCTTCAGGTGGCAACCGATCTGGGCTACAAGGTCATTCAGTGGGATACTGACTCGCTGGATTGGAAAAACATCGGCGTGGACAATATCGTGAGACGAGTGACCAGCAAGGCGCATCCCGGTGATATTGTGCTTTTGCATGCCAGTGATTCCTGCAAGCAGACCCATGAGGCCCTTCCTCAGATTATCGATAATCTGCGCAGCCAAGGTTATGAATTTGTCACTGTCTCCGAACTAATCAGCCAGGGCAGTGCTGAAGGTAAAGAAGTCCGGGATTCCGCCATGTTAAATGATGGTTTGGAGGATGCCGCCGGGATGTAGAAATCAAGGTGGTATCGCAGTGCTCCTGGTGCAGATGCGGGCCAACAGTTATTAATGTCTTGGAGAGATGAGCTGCGAAATATCGGGTGTGGGGGTATCCAGTTTCGGGTAGCTCAGATCCAAGCCCTCCAGGGTTTTGACAACAATGGCTAAAGCCAGGTAATTGCGGTACCACCGGTGATTGGCCGGAATCCAGTACCAGGGTGCGGTATCTGTACTGGTTTCCTTGAAGACATCATCATAGGCTGCCTGATAATCATCCCAATACTGCCGCTCCTGCAGATCACTGGCATCAAATTTCCAATGTTTGGCCGGGTCCTGCAGCCGTTCCTGGATCTTTTCAAGCTGCTTATCTTTGGAAATATGCAAAAAGAGCTTGATGATGGTTGTGCCTTCTTCAGCCAGCATAGCTTCAAACTCGCGAATGTAGCGGAAGCGGCGCTTCCTTTCTTCTTTTTTCAAAGTTCCATGCACGCGCGGCACCAGAACATCCTCATAATGCGACCGGTTGAACGCGGCGATGTATCCCTTGGGCGGCGTCTTCATATGCACTCTCCATAGAAAGTCATGCGCCTCTTCCTCCAGAGAAGGTTTCTTAAAGCTGGTGACCATGAACCCCTGAGGATTAATGCCGGAGAAAATGTGCTTGACCGTGCCATCCTTTCCGCTGGAGTCCATTCCTTGAAGAATGACCAGCAGGGAATGCTTTTTCTGGGCAAAAAGGATATCCTGGAGTTCGGCTAGACGCTCTTTGAGCTTTGCCGTTTTGGCTTCCGCCTCTTCCTTGGATTTAAAGTCCCCGCTCTCGTCGGGGTCGAGTTTTTTCAGGACAGATTCATTTGTGTCTTTTATCATATAGCGCTTGATGTTCATATATTCCCTCCTAGTCGTCTCAACCGTTTTTTAGTTATGTAACTGTTCTTAAAGATTAACCTGATGCTTCCGATTTTAATCGGATTAAGTTCGGACACCAACGCCGTCCTGCTTATATTTTCAACAAAACCCCGACTTCTCATGACTGAGGACCGGGGTTTATGGGCTGCAGCTTATGCGGATATCGGCTTCAGGATACGGTGCAGCATCAGAATTTGGAATGCATTGCAGGCAACCAGCGGAATCACAATAAATACAGTAGCACTGTCCACCCCAATCTGAAGTACGCCAATGATCTCAACGATGGTGATGGCTGTCATAAAGAAAAATGTCGGAATCCAGGCTGTGAGGTTCGTGCTCCGCACTTTGAAATAAGCAACAATAAGGGCAGTAAGCAGAATGCCGATGCCTAAAATCCAATCGGAAGAAACATCCCGTCCGCTCCCTACAAAGGTACGCAGAAAAATCAGCTCAAGCAGTGCAAGTACCGCCAAAACTACCTGAACGTATTGCCAAACCCTCCGCGGGAACACCCCGATTCCCATGTAGTTCAGAATCAGATACGCAAAAAACCCCAGTTGGGCGTAAACGCTCACAAGCATACCGTAGCCAAGGAGAATCAAAGGGTAGATCAAAGTATCGGCTGTGCTTTTAAAATGAATGGTGCCGTTTACGGTCTGCAGTGCCAATCCGGCAATGACTGCCCCTCCAGCCCCGATCAGGAGCGTCGTCCAGAATAAAAAAAACCATTTCTTTATATTCAGCCTGTTCACCTCCCACATGTCAGATTTATTTTACCAAGCTTACCGACAAAAAACCATTGCCAGGCAACATAAAAGCTTGTCTCTGCGGCATACTACATGCAGGAATCCTATAAAGGAGGGCAGCGCCAATGAAGTGGAGGACTTTGTGGACTGGAAGCTTGGTGCTTAGCATGGTTATGGCCTTAACGGCATGTGGAAGCGAACAGAGCGGTTCCTCTTCCGGACAAGTCAGTTACAAGGAAATGAAGACCATGGTTGTAGATATATTGAAAAGCGAAGAGGGAAAAAAAGCCGTCGAGGAAGCGATGTCCACTCCAAGCTCCGGCACCGAAGGAACCAGCACCAGCGGATTAAGCATGAAAATGATGCCGCTGCAAACCACTGAACAAATCCGGGTCGCGGTAAAGGACACCATTACAGCACCGGAGTACCAGAAGGAAATTGAAAAAATCATGACCGATCCGAAGTTCGCAGGTGACTTTGCCAAAGCGGTCAACTCACAAAGCAAGGAGCTTCACCTTCAGCTAATCAAAGATCCAACATACCAAAAGTCAGTCGCCGAAATCATGAAATCACCTGAAATGATGAAGATGTTCCTTGATCTTACCAAAACCTCCGATTACCGCAAGCAATCCATGACCATCATGCAGGAAGCCATGCAAAATCCATTGTTCCGCATGGAGGTGCTCGATCTTCTAAAGACGGTGGTGCAGGACGAGCTGCAGCCTAAGGTAGAAAAAGGCGGGGAAGGTAAAGAAGGACAGGGAAAGGGGCAGGGGCAGGGCGGAAAAAGTAAACAAGGCGGCGATGATTCAGGCTCCTAAGACAAAAGAGGCCCTCCCGGTAAAGGGAACGGCCTCTTTTGGTTTACTGCTCATTGTTGGCGATCAGCTTGTCAGCAATTTCAGCGAACAGCTGCGCCGTTGCGGTCTCCGCCTTATATACAGACGGTGAGAAGTCCGGTTCTGAAATGTGATTATCCGGTGCACCCAGAGGTATTTGGGCCAGCAGCTCCGTATGCAGGGTTTCCGCAAGTCTTGCTCCGCCTCCCCGGCCGAAGATATAATCCTTCTTTCCGCAGGACGAACATTCGTAATAAGCCATATTCTCAATGACTCCAAGGATCTCATGATCGGTCTGCAGAGCCATTGAACCCGCTCGGGCCGCTACAAAGGCTGCTGTCGCATGAGGGGTGGTAACGATGATCTCCTTACTGTGCGGAAGCATCTGATGGACATCCAGTGCCACATCGCCTGTACCTGGCGGCAGATCGAGGAGCATATAGTCAAGCTCGCCCCAGCCGACATCGCTGAAGAACTGGCGGAGCATTTTGCCAAGCATTGGCCCTCTCCAGATCACGGGGCTATTCTCGCGGATAAAAAAGCCCATAGACATAACTTTTACTCCGAAACGTTCTACAGGAATAATCGTTCCTTCTTCCACGATCGGTCCTTCTTCAATTCCCATCATATCCGGAATGCTAAAGCCGTAGATATCCGCATCAATCAGTCCGACTTTTTTGCCTTTCCGGGCCAGTGCGACCGCCAGATTAACGGTTACAGTAGACTTGCCTACTCCGCCTTTGCCGCTGGCAATCGCGATGAAGTTCACTCCTGAATCCTTATTGATCAGCTCGTGCCCCTCAAGGCCCGCTGCGTGGCCTTTTAGCGCCCCGCCCTGTTCCGGCTCCGGCTTGTCCTCCGTGCTCTCTCCGCGAAGGATAGAGCGCTCATAATCGGTTGCATCACGCAGCCGGATATGAATATTGCCCGCGCCTCCTTCTGTCAGCAGATCACGAACCTTCTGCTCGAGCTCCATACGGCTTTTCTCATCGGTATCCAGACATACGAGCGATAGGGAGATCCGGTCTTCTTTGACCATGATATCGCGAATCAGCTGCAATTCAATAAGGCTTTTTCCGGATTCCGGGTCAGTAAGCGGCTGCAATAGTTCCTGAATTTGTTCCCTGGTCAGCATGGAAAGCACCTCAATTTTCTCTCCGGACGGGTAAGGCTCCGGTATTTTGGATCTATTATAACATTACCCTTCCGCAAAACGTAGTAACGGCTAAGGCTGTTCCGAGGCGTACCGCAAAATCCCGCGGTAGATGCTGGTGGCCACCTTCCGCTGGTAGACATCGTCTCCAAGCAGCGCCGACTCCTGTGGATGGGACAGGAAGCCAACCTCCACAAGCACAGCAGGCATTTTCAAAGCTTTCAGCAAATATACAGTATTTACAGTCTTGGCTATCCGGTCGGTATTCTCAAGTGTTGCTTTCAGCTCAGCCTGCACAAAACCCGCTAAAGCTTTGTTGCCTGTGTGATTCGGGTAATAGAAGGTCTGGGCACCGCTCCAGCGTCCTGAAGGCACACTGTTCATATGCACACTTACAAACAAATCTGCCCTCTTCTCTTCAATGCTTCTTACCCGTTGCTTCAGGTCTTCTGTTTTCCGTTTGGCGTACCCCTTCGTATCCTGCCGGGCCAGGTCGTAATCCCCTTCACGGGTCATAACCACTATCGCTCCCGCCTGCTGCAGGTAATCCCGCAAATATAGAGAAACCGAAAGGTTGATATCCTTCTCAATCAGGCCCTCCCGGCTGACCGCTCCCCCATCAGGGCCTCCATGCCCGGCATCAATGGCAATGACTTTGCCCGACAGCGGCAGACTCCAGTAATTCAGTGTTTTGGCGGTTGGCATATCATAGGCAATAATACCGATCATCACCGCCAGCAGGACAGCACCAAGCATGCCTTTTTTAATGCTGCTCCACGAGATCCAGACCGAGACTTTCCCCTGCTTTCGGCCAGACATAACAAAGACCCCCTCGTCCCGATAGATTCTACTCATCTATATGGGACAAGAGGGCCAAATAGTACTGGCTATTTAGGATTGGGCGGTGACTTCCACAGACATTCCCTCGATGAGAATCTCTGCTACTTCAGGACGCGTAAACTCCGGAGGCGGACACTTGCCTTCCCGCAGAAGTCCCCGGACCTTGGTGCCTGAAAGCGTCAAATGCTGATCCCCCGGATGCGGACAGGTTTTGCTGGAAGCCATGTTTCCGCATTTTACACAGAAGAAGCTGTGTTCAAAAAATAGAGGAGTGATTCCCAGCTCTTCCGCCGTGAAATTCGAGAAAATCTCTTGAGCTTCGTAGGTGCCATAGTAGTCACCCACCCCCGCATGATCGCGGCCGACAATAAAATGGGTGCAGCCGTAATTTTTACGCACCATCGCATGAAAGATCGCTTCCCGCGGTCCGGCATAGCGCATGGCAGCGGGGAACACGCCTAGAAAGGTGCGGTCCTTTGGATAATAGTTCTCCAGCAAAGCAAGATAGCTCTTCATGCGCACATTCGCCGGCACATCGTCAGACTTGGTCTCCCCCACCAAAGGATTAAGGAATAACGCATCCACAACCTCCATAGCACATTTCTGAATGTACTCATGAGCGCGGTGCACCGGATTGCGGGTCTGAAAGCCTACAACGGTTCTCCAGCCTTTGTCAGCAAAGATTTGCCGTGTCTGTGCGGGATCGAAGTAAAACTCTTTGAACTTCTCAGGCGCAGGACGGTTCAGAACGGTAATAGGCCCTCCAACATAGGTTGACGCTCTAGCCAGTAATTTGCTCACACCAGGATGCGCAGGGTCCGTCGTTTTGAACACATTCTGCGCCTCAAACTGCTGATCCGCCTCATAAATACTCTCAATATCGAGCAGTCCATAAATAACCCCGTCTTCCTCACCGATCAGCGACACTCTTTCGCCCACGGCAAGCCCGGAAGCCGCTTCATCCTCGACAGACAACGTAACCGGGATGCTCCATACCGTGCCGTCAGCGAGACGCATGCTTTTGACAACGGAGTGGTAGTCTTCTTCATTCAGAAAGCCCGTAAGCGGCGAAAATGCACCGACCCCGATCAAATCCAAATCCGATAAAGTCCAGGTATTCACAGGTATTGATTTGTAACCTGAAGCCTGCTGAAGCAGTTCTTCTCTGTGTGCGCCTTCAGCTACACGTCTAATCAGTGTTCCTCCATGAGGAAGTATCGAAGTCATTTATGCGCTCTCTCCTTCTGTGCAATTCAAATTCTGTTCTTATTTATGCAGTCCGCATTCTGTTTTATCTGAACCTGACCATCTGCCCGCACGCGGATCTTCACCCGGCATAACCGCCCGTGTACATTGTTCGCACCCAATACTCGGGAAATTGCGATCATGCAGCGGGTTATAAACGACATCGTTCTCACGGATATAACTCCAGACATCCTCGGAAGTCCAGTTGGCAATCGGATTAAACTTAACAAGACCGAACTTATTGTCGTATTCGACTTTTTTGGCATTGGCCCGGGTGGGTGCCTGGTCACGGCGGATTCCTGTAATCCAGGCATCATACTGCGACAAAATCCGGGTAAGCGGCTCTACCTTGCGGATTGCACAGCATTGATTGGGGTCGGTGCTCCACAGCGCCTCGCCATATTGAACGGCTTGCTCTGCCGGCGTAATCTGCGGCGATACACGGACAAATTCCATACCGTATTTATCGGCCATTATATCTCTGGTCTCATACGTTTCTTTAAAATGAAAATCCGTATCCAGATAAAAAACATCTGTGGACGGACTGACCTTCTGAAGCATGTCTACCAGCACTACATCTTCGGCACCGAAGCTGCAGGCAAAGGTTATATTAGGAAAAGTCTCTACAGCCCAGCGGATGATTTCCTCCGGTGTTGCATGTTCCAATTCTTCGGCTTTGACTCTGATTAAATCTTCTTTCTCCAATAAGTTCATTATTATATTCCCCCATCCTGGTATTCCGCATAACAAACAAATCCGCTAATTCCAACTAATCTTATATGGAATAGTATAAGACATTCAGGGCTGAAGTCAATAGTTTTATCCATTTTGGGTGAAAGTTGTGTACAGAGTTTGAGCGCTACTGCTTCCAGGTGTTTCTGAACAAAAAAGTACCCCGCCGGCAATCCGGCAGGGCCAATGTAGACATGAATGATTATGATACATACTAACTCGGGATATCTGTAGTATAAGGGAGAAATGTTTTTGGAGTATTTTGGGGAATGGGTGGTTTCTTAAAAATCCCTCCACCCGCATAGCGGGTGGTTTTTTGTTTGCACGCTTCGCGTACTCAACTCGCTGAGGCCCTCATAAAAACGCCTATACGGCGGTTGCTTTTGTAATCTCTTTAGCTTGTTTATCTGTGATCTTTTTGGTGGTTACAAATACCTGCAGTTGCTCCCCTGTATACAACCCCGCGTCAAAGTAACGCTTAACCAATGCGTACCAGTTCATTTACAGCACACCTCCTTCCACGAGACTCAGGAGTAAAGCAGCCTGATCCTTCTCCACTTGATTTTGCCTTGTTTGTGTCTGCACAAGCTCCAGTAATAAAGTTGCGTTTTCCGCCTCTAAACGAGCCATTCTTTCAGCGTCAGTCTCTGGTAACTCCGGTACTGGTTGTGCTTGTAATTCCTCCCATGCCCTTTGTAACTCTTCGGTTGTAGGTTTCGGGGTATCCGTCTCCCACACTCCGATGTATGGTCCTTTTCCGTCACTGTCATCCCATATTTGAAAGTCTTTTTTAGGCTCTAAATCTGGATACAGGTACACCATCGCGTCAAACATATTCATGATAATTGCCCTCCTTTAGTCCGCTAGTTTCGTAATGTGCAAGTATCCGGCATCTGTACTTGAACCCCACAAATTCGTTCCGCCGAAAACTTCGACTCTAATGTCCAATGCCCAACCAGCAGTCAACCATATCATAGCTGTGCCATTTAATGACAGCGTGTTACCATTGCCTGCAAGTGTCGCAAGGCTCTTATGGAACGCATTATTAACAAAAATCTTTAAATTAGCACTTGCATTTGTATTTATTAAGCCTTTTACAAAAGAGGAAACGAAATACCAACCATTTGTCTGCGCGGTGTATGTCCCGTTTGAAAATTCCCCCCTGGCATCCCCTTCTTTTGTCGAAAAAAGCAACTTCGTCATGACGTTTGAAGCGATAGGAGTATCAGCCGACAAACGCGCGGATACTAGCGGTTTATAACGATATGCATTCCAAAAATGGGGCAGCGACACCATTCCATCAGAAGTGGTTTTGAAATACGCGTCCCCATTCAATTGGAAAGGAAGCTGACCATTCGAATAAAAATCAAGTCGTCCATCGGTAACCCAATTGATCCCGGTATCGCTGTCGCCAATAGGTAACGTAAGTGAACTAGATGCACCGTATGCGGTATTTTGGGCAACCCATAATTGTGTGTTGGTAACGATGCGTCCGCCTTGAAGTGATAGAGTACCGTTCCCCGTTCCGTTTCCACCATCTGCTATGATTCTTGCGTCGAAGTCACCGGCACCTGAAGTATGAAAGTCAATGTATGACACGCCCCCTGAGCCTCTGTTTGCTCCAAGCTCTAAGAAAATGGAGTTACTTCCATCTGCTAGAAGAAAGTCGCCGGAATGGTGCCCGTCCAGCAAGTCAGCATCTAACTTGCTGCCTGCACCATCTACAGTCAATAGCTTGGCAAGTACATCACTAGCTGTATAGGAACTAAGCGGAAGTGGGACAAACCCCAAAGACGCGCCCATAACAGGATTTTTGTGGACACCTACACCTACACCGCCCAAAACAACTACAGGCAGCGCAATCTGAACGACATCGCCAGCGGTGGCGTGTATATAAGGCGCACCATTACTGTAACCGCTGCCTGCGCCAATTACATTTTCGATGTGCATCCATCCATCGGCGCTAGTTAGCTGTACAGGCGCGGACTGGATCACTCCGTTCTTCCGAAGCCTGAAGTCCTTATCTATTACTACACGTGTCCCCGTTTTTAATCTAATCCAAAAAGATACCGTGAAACGACTAGCGACTCCACCCGCAGGCATGCTACTACAAGCGGTCATCAAATAGGCTGTAGGAACGGTTGCATTAGGACCATATGTTCCAGGCCCCATTGTGTATGAGGCGATATGATACTCTGGGCCATATCGAGTACTTCCACCAATCGCGGTCACTAGACTGGCTACATCGCTGTTTAGTGAACCTGCTGCACCACCGTAGGTTGAGTTGTCATATATAAATTTCCCGCCATCCGCTACAGACGTTCCGTTCCATGATGAGAAAAAGGTGCTATTCGCAAAAGCGTCGGAACATTTGTAGTCCTTTGGGTCATTTTCAGGGCCTACGAATCGTCCGGAATCTCCTAACATGTTTATGACTCCACCGTAGGTCAGTGTATCGGCTAGGGTTGATTTTAATGCATACTGCGTGTGCGGGTCTCCTGTGGAGTTATGCGTATCTGCGTGCCAATACTCACTCCAGGCGCTCCAGGCAGCATTGTTTATCTTGCTTCTTCTGAACTCTCGTGTCGTCCCAGCGCTTGAACTTGCCACCCGGGCAACTTGAAATATCCAATTTGACCCGTTATAGGTGCCGCCATCACTCACAGTAACATCCAAAGTGCCCCACAGACCAGCGACAGGTGAGTTAGCGACGGAATCTGAGTAAATATATTTTCCATGTACAAGCGCTGCACCAGCGTTTAGGTCAGCAGATATCGTACCTGCTGCTTTGCGCTCAAGTTCACTTACTTTGAATCCACCATGAAGCTCTGTGTTTAGCCCTGGAACCATTGTGTTAGATGCGACTACAAACGGGGCTGACCCACTGGGTGCACTTGATACGAATTGTACGCCAGTTAGGTTTCCACTTCCATTTCTCACAGCTACCGTATTGGCAATTGCGGAGAATGATATACCATACCCGCCAACATACTCAGCATTTAAGTTAGGGACTAATGCGGTGGTAGATGGTCCACTGGAGTCGATGACTTCCGCCCAATTTCCCCACACATCGTTAGGATAGTAAGCCATCCTGCACTTTACAGGAGCTTTGACATTATACGGATAAAAGTATTGAATTGCGGACACTCCGCTATCGTATCCCCTAATGGTATGAATTGTGCCATAGGTGCTCGGCCATCCATTACCACTTGCATTTAGGGCAAAGAATATACTCGAACCCACCGGATATGTTGACGGTAGAGCGGCGGCTGTTTTGTAATCATTCGGGTACGTCGCTGGGTGCAGATGATCTTCTCGCGCATACTTTTTCGATGTGCCGACTAGCCCAGAATTGTTGAAGTCACGCCCCGGCGCAGCGGTTCCGGCCTGATTCAGCACAAATTCTGCTGTAGCTAATTGTTTAGTGCTTGTATCAGCCGCAGGTGTTGGGCCTGTCGGTGTCCCAGTCAGAGTAGGAGAGTCTAAAGGCGCCTTGGCGTTCCATGTGGTTCGTTCTGCTGCCGTAATGTGCCGGATGGAATCATCCGCGTGGACCTTGGCAGCCTCCAGCGTTGTGGCTGGTGCTGTCCGCCAGGAGGATTTACCTGTAATGGATTTGATCATATTTGCCAGCAAGCCCAGCAGAGTAGTCGGCGTACCAGTGTCTCCAGTTGGGGCTGCGGCGTCTGATATGGTCCGATTACCAATTATCGTATCTGTAGCCGCACCATCCATAAGCTGACCGGCTCCCACTGCCTTATCCCCAATCTTTGCTTGCGTGACTACCTTCGCTCCTAGCTGCGCCGTACCCACCGATGAGTCAGCTAATCCTGAAGCTGTTATCTTTGGTCCATCCCCAGCTACTCCAGTATGTTTATGACCAGTCGATACATTAAACTTTGCCGTGACCTCGGACTCCCGAGCGAAAACAAGCGAATCATCAAGAGTTGCTGTAATATTCGATGCTGTTCCCACAACAACAATACAGTCAAACACCTTTTCAATAATGTCCGTTCCACCGCCGGGGGCGATATAATCCGCCGTTACCCCTGCATTAGCATAAGCATATAGAATTTCCCCAGCGTCCGGATCCTGCGCGAAAACCCCAACCTCCCGGAAATAAAATCCGGTTGTGATATCGGCATTTGAAAGAGAGGCACCTATTACCGCTTTATTCGGTGGTTGCGTCTGAAGACGGGTGATAGATAGGCTCTTTTTTTGTGATATCAGAGCATTCATCGCGGGGATGGACTGCCCGCTCAGTACCCCATCTCCGATGGCTATGCGAGTATATTTGAGCTGCGCCCCCGCCTGCGCCTTGCCTTGTAGCACGAGGCCTTTATTTGTTAATGTCATGCCGCCAAATACTGCCACATGTACCCCTCCTTAAATCGTAATCGTTTCTCCAAAATGCAAAAAACCGCCGAAGTATAACGGCAGCTCTTCTGCTTGTGATATTGTGACGCTATCCAGGACGGCGGACAGTCGTTTGACTGCATCCACCGCCGAGACAAACTCCTGCGCCCGGATGGTGGTTACATCGGCGTTGTTGGTCACAACCCGGAAATGATACGGGTCGCCACCGTACTGCCACCACTCCTCCACCGCGCCCTCACCAAAAAGTATTGCAATCAGATCCTCGACTGCTCCCGCCGTACCTTTATGCCGATGGAATGCAATCGCATTTTTGATCAGTAACCGCTTTTGATCCAATGGTAAATCCGGATCATAATAAGGTGGGTTGTATTGCCATGCCAGTTCATCCGTTTCCGCATCTGTCCACTCCGCTGACCGTCCGAAGATATCCAGGGCTGCAATCATGTTGGTTATCCCCTGCAACTGTGTATCCAGTGCGATCGCTGCAGCAGCCATAGCAGAATCATTGCGAATGGATGGCGGCATCAGATCAAGCAGGCTTACTGTCTGTATATTAATCATCAACCAACCCTCCAAAGGTGATTGTCGTAGTGCCTGTCTGGGCAACCTGGGTTGCGGTCAAGATCGTATATACCGGCGCTGTTGGCACTACCCGTTGCGCTCCGGCAGCCATGATGCGGCTGATCAGCTCCGATGGATTAACATGCCGCCCAAGCTTGACCTTTTGCCACCGTTGATATGCAGTGACTGCCGCAGAAATCTTCTCTTGGATGCTTGAAACCTCCGAAGCCCGACTGCGGCTGATGTAATAAGTCACAATCGTGTTATAGCTTACCGGTTGCGGCGCACTCACTGTAACCAAATCTGTTAATGGCCGGATGCCCCTATCTTCCAATGTCTCGGAAATGGAATCCAACACATCCTGACTAGGTACCTCACCATCTGCAAGTAAAGGAACGACGGTTACGCGTCCTTCTGCTGGTGAGTAAGCATGTACATCTATGATTGCGGACGAAGCTGACTTTGCCCAAAACTCATATGCTCCCTGTGGGCCAGCTGTTGAATAAGATTCAGGCGCATTTCGAATACGTTCTTTAAAAGCTTCATCCGTTTCTGCAGCCGCTCCACCGGAACTAATCGTCAGATTGCTCACAGACTGGACAAAAGGAAGCGGATCCATTAGAACATTAATCTGTCCAGGCAAAAATCCATTCCCTATAGCTCCTGGATCGGAGCATACTGCTGTTGCTATACCGGCCGTCTCACCCGCTGGGATCTCTACATACTCAGTAGTTGAAAAAAATATCGAACCGTTACCACCTTGCGCTCCAACACGTGTTCCTGTAGGGATTGAGGTAGCCGAGGCCAGCGGAATGGATAAAACGAACTGTAGTGTGACAATTGCCGCTGATGCATTCAGCCGCTCCGAACCCTGAAAAGCCCCCATGTGATCAAGGACAGCTCCAGAAGCGTAGCGCAGCAAATTCCCTTTAGCCGTCTGGTTGATAAGCACCTTCTGCTGGACAATGATCGCTGCAAGAGAAGACAAAAAAAGCCGCACCGGATCGGCGGGCTGCAATGAGCGTCCAGCAAGGCCTTCATATACAGTGATCACATCTTGCTGGATGGCAGCGGCGTCCTCTTCAGAAAAGAGGATATCCGGTAGTTCAGCATATTCCAATTACTATTCCTCCTCTACCAGTGTATATTTCACCACAACTGCCAGGCAGCCGTTCAGAGAATCTTTTATATCATCCTTAAAAGAAATCTCTGATACCGAGGCGCGTGGCTCTTGTTCTGTAATAGCAGTGATAACCTCTGCGATCAAGCGTGATTCGGCGATGGATGCCGGCTCATCAATAATAGTGTAGTCCAAGCCAATTCCCCGGGCCAATGGTGCGCACCCCCGTGGAGTAGTGAGAATAGTTCGAATATTCTGAGAAACTTCTTCTTCCACCGTTTCCGGTGTGAAATTGATATGTGTAGGCTGCGTCATATCCACGGTATATATCATTTTACATACTCCTCAAGTGAAATCGTGACCTGTGCGTCCAAAACATTACCAATGCTGTCCAAGGTATTCCAATCCTGAGACAAACCAGTAATGACCCAAAGCCCTACGCCCACATATTTGCGCCCGATGATCAAGGGCAGAGCTTTACCGGCACGGTCCAATTCCGTGAGCTTATCGAGCTCCTTGCGGGGATTAAGACCGAGGGCAGCGGAAAAACGGACTGAGAACGAGACCGAATCCGATCCAGGACCAATGAATTCCTTTTTGGGCTTCTTTCCAATAATGTCATGCTGTGCCCACCGGCTAGAACTGCTGCGCTTAAACTCATCAATGGTTCGAATCGCTCCTTCCGCGACAACAAAAATGACAGGCCCCAGGCTGCCGATCTTGTTCATCCTATAGTCAATATTATTATCCGGCTTGCTTTGGAGATGGTTTAGCTGATCCACACCCTCCATTATCATGCCAATCATGTTCATCCTCTTACACCCCGCCCTTCGTGTTGAATACGTCGGCCGATACTATGCCTGTTACAGTCAAATCACCTTCGATCTTCATCCCGCCGGTCCCTTTGATATTCAGTCTTTTCGCCGTCCGGTCATAATAGACATAGCTGCCGTCTTCAAACCACACCCCGCGCTGATCTTTTGTACCGGAAGGCGGGTCATCTTCTGCAAAATAAGTCCCCAGACAAAATCCGGCCGAACGCCCGTTATCCAAAAAAACACACAGTACTCTCTCGCCAGGCAGCGGGATGGCATTGCCACGCCCCCAACCGCCCGGCGTAATGACCGGCAGCTCTCCTGAAACCATATCGTCACGATCTGCAAAAGTAACCCTGACACTTCCCGCCACCGCATCTGATGTTGATACCCGTCCAATTAGGATCATCTTACCACCCCAATACTTTGCGAATTTCCAAATTAGTTGTATAACCACTACTTCCAATTGAGTGCTTTGCGGATTCAATAATATATTTCCCATCAAACCGCTGCCATCCCTTGATATTGATAGTTAGTCCTGTGACCATCCGAATATCTCCCATCAGAGAAAGGGTCCCTTTCCCCCCTTCTTTATTTCGCTCCCGCAGCCTTTTACGGGCTAATCGCAATGCATCAGCCTTAGTATCAACTTGCTCGTTGATCTTAAGTACAGGTCCATTCTTTGGTGCACCGTTAGGTGTGTAAGTTGCTTTGAGAGGTTCTTTGCTCGTAGGAGGAGTATAGGTAACCGTACATGCCCGGAAAGCTGCATATGCAGTGTTCAACGCAAAGCTATAACCCGTAACATTATCATCTCCCCGTACAATCGTTGTAATTGCTTCTTTTTGTTCATACACCATTTCATCAAAGAGAATCAGACTTCCTCCAGATACTTTGATTGCTATGCCTTCTTGAGTAGCTGTGTTCAACAAAAAGGCCAAATCCGACATTTCCGACTGCTCCAGACGTTCATAAGAAGGATTGTCCTGAGCCTCATATATTAATTTCAGGTTAGCACGCTTAGCAACTTGAGCGGCTACCGTTTTTAAATTGGTTTTTTCCCAACTGCGTGAACTGCGCTGCATCCGAATTTCTGAACTGATAGGAAGTGAGACCGCCTTAATGGATATAGTGTCAGGGGGACCATTAAAATCAATACTGTCTATCTCAAATGTTCCAAGTGGCAACTTTTTGTTTTCTCCTGGCTTATCCCAATTGATGGTTCGAATTGAAGCATTAATCTGATCACCTTCAACCGGTACCCAAGGGCCTTGCCAATTTCGTTCCCTATCCTCAAGCGAAACAGTAAGATCATCTAGAGAGCCGGATACAGCATCATTATATTGAAAGTCGGTCAGAGACTTTGCGATGTCCATCGTGATGTCCTTTCCGTTATACTTAAGCTCCAGCACCGCCCTGCGTGCGTCTTGCATCCATTCCAACTTACTCTCACTCCCTTCGCCAAGGAGGCAATGAGTTGGTTAATTCAGAAGGTAAATTTGGCACTTTAAGAACGATATTTCCAGAAAAAATACTGACGTCAGCTTGTGTAGGGTTAGCATTTAAGAGCAATGTCATGAATTGAACATCTCCATATAACTTGAACGCGATTCCGTCCCAAGTATCACCTTGCACGGTTCTATAGATCATTGGAAGCTCACCCGCCTTTGTTGTTGGACCATGGCTTTGAAGCGGCGTTCAAAGCTATCCTCCGTCTGCTTCAAGGCCTCACGCAATTGTTCGACCATAGATTTATCACCGCCCTGCAGTGATACATTCGGTGCCCAGGTTACATGAATATCCCCTTTACCGCTGAACCCGTCACCGTAGCCCATCAAATCATTCGCCTTTTCTAATAGAGAGCGTGATCGCTGTTTACCATTCAAAGGAATGGCAATTTCGGGACCCGCTTCGCCAAATATAGATGGGACGTTAGCAATTCCTCCTTCAGCATACCCCTCAAAATCCGGATCATGCAGTGCCCAATAAATTGCCTTCTGACCGGCTTTAGTTTGCGAATCGGGTTTGCCTTTGGTTTTAATCATCGCTTGGACATCGTTCCACTCATCATCCGAAAGCCTGAAATTCGGAATCTGCCCAGTCTGCTCCCATATGAGCTGCAAATTCACTTTCTTTTCAGCAGGTAGTTTATCCACCTCCGCATTAAGATTAACCATGTAACTCATAGCTTGATTAAATTGCTTTTGCTGGGCAGCGGACATATCCTTGTATTTCTTGGCTTGTTGCTCCAGAGTGCCTCCCAGGTCAAGCTCGATCATTCGTTTTTGTAGATCGTAATAGGAGGAAAAGCTATTTTCAGCCTCGGTCATCTCACTTTGGGTTTTCTTAATCTTGGTATAATACTTATCAAATGAACCTTGTATTTTTTCGTAGTCTTGTCTAACTGTTGCAACAGCAATACCAGCATATCCACCATAATCTGTACCTTGAGCCTTATTGAGATTCTGCAGCACCTCATCTACTTGTTGCTGCTTCTGCTCATCATTTCCCTGACCGCCCATAATCTCATCCAGTTGATTCATGTATAAATGATAGTCACGAAATGATACTTTAGACTTCTCATAATCAGAATTTTGTGTGCTGAGGTTTTTGGTCAATTCTGAATACCGGCTTTCCAAATCAGGCAATTTCGCTTGTGCTGAAAGTGCGTCATGTTCCATCTCGCGACGGCTCATTTGCTCATGGGCTTTTTTAATATCCCCGACTAACCCCAACTGCTCGCGGAATTTACTATTCTTAGAGCCTTCTGCAGACAAAATATCCGGATTCATTTCGATAAGCTCTTGTTCTACAAGCTGTTGTTTCCTTCTAGCCTCAGCCAATTCGTCCGCAGGAGTTTTGGCATTTTTAATTTTTTGGGTCAGACGGTCATATTCCGTAATGAGATTCTGAGTCCGTTTGCTTGCATGGTCGATTTCTGCATAATTAGAGTAAGCTTTGTCCAATACGTCCCCCATATTCAAAAGCTCACGCCGTGCATCTTCCTGGTGCTTCTTATAAGCAATAACTCCGGCAGTGAGTAAGCCTACACCTGCTACGGCGATACCAACTGGATTCGTGAGCAACCCCAGCGCACTGGCGATTCCTCCGGCTGCTCCACTAGCCCCTCTGGCCGCAGTAACGATTTTAGAAAATTCTTGGACAATCTTCACTGTTTTTGTAGCCAGCACCGCAGCAGGAACTGTAAGACCGATTACCATCAGCGACTCCTTATTGTTGGAAACCCAACTGGTCAATCCCTGAAGTGCAGGCATTAAGCTTTCCGTTAAGGGAATTACAAGGTTTGCCTGCAGTTCCCGTCCCATTGCAGCAAACTGCTCCGAAAGAGTACTATCTTTTATCTCAGCTGCTTCTTCCAGGGTTTGCCTGGTCATATCAAACTCATTTCGGGTTTGACCAAGCGCCAATACTGCCTTGTTGCCCATGTCTTCGAACTGAGATCCGAACAAGGAACCGGCAAGCTTCGCCTGATGAATCGGCTCCTTGATCCCCTTTAATTTAAGAATAACCTGCTCCATCGCTTCCTTGCCGGTCATAGATCCGTCTGCCAATCCTTTAAAGATTGTATCACCGGTGCCCAGCGTCTTTTGCAATTGAAGCATAGCCTTGTTTGCGGAATCCCCGCCCGACTTAAGATCTCCAACAAGTGCAGCTGCGCTTGCCTTCCCTGCAACTTTTACAAGTTGAGCGAATTCTTTCGATTTCGTTCCACCACTAACAAGTGCTGCGCTGAATTTTTTCAGTTGCTCAGGTGCAAACAGCTCATAAATTGCAGCCTTTGTGGAATCCGAGCCGTTTTTAATTGTTGTTCCGAATACTTTCACAGTATCGGCAACACCATCAAGCGAGCTCGCTCCATTCTCCATGCCTGCACTCAATAATTCGAACATCTCGTCGGCAGAATACCCCATTTTCTTGAAATCAACACTGTATTTCTCTATTGCATTCAAGAGGCCGCCGGATGTGTTCAGCCCCTTTTGAGCGCCTTGGGCCATAAGATTATACGCTTGTTCAGAGGAGATACCGAATTTTTGCATCATTGAATCAACTGCTTGCAGAGAGCCAGTTATGTCCTCTTTAAAGACATCACGATACGTCATGGCTGTCTGTGTTGTCTTCTCCAATTCATCCCCTGTTTGCTGCAAAACTTGCTTCACAGCTCCTACGGCGTTACCAATATCCTCAAAGTTTTTACCGTAATTCTGACTGTACAGGTTATTGGAGATTTCCTTCATTTCTTTCATTTCCTTCGAGGACATTCCGGTTTCAGCCTGTAGCTGCGCCATCGCCTCGGAAGATTCATTCACAGCAGTCCATACCGCCTTCAGCGGTTCCACTGCTTTATTAAGCATTGAGAAATCAATTTCTTTTACTGCATTTTTAAGTTTGTCGCCGAATCCTTCGACATTTCCACCTGCATCCGCGATGCTGTCATCTGCCTGTTCAACCTCTCTTCGAAGCGTATCAAAATAACCGCGCCTGACCATCTCCTGCAGCGCCTGATCTAAACCTTGAACCTGGTGTTCGGCCTCCTCGACCGACTGACGAAAAGCAGGAGTCACGAGCGCATTCAAACGGAAAACAATCTCATAAATGCTGCTGCTCAAGCTGCTTGTCCCTGCCATAGGTCACCTCCTTCCTTTAATCCGGGTCACCCTCTCGACCCAATCCCCCAGTTCCTCAAGAGGCAAGGCAAGGAAATAAGGAATAGGGGTATGGGTGAGCATGGCTAAGGAGACAGCGATGTCTTTGATCCCATCGCCGTCCCCGCAGCCTACAGCAGCAAAAAACTTTGCGCCCGCAAGGTCAGTTTTGTAAAGTCCTTGGCTGAAAGTGCTCTTATCAATCCAACATGAACGCCTGCAGCCTTTGCTACAATATAAGCCTGATAGGCTTTATTGGTTTCCTTGATTAGTTCCCCGCTTGATTGCCGGGCTGCTTCAGCTTGATACTGCCTGTCACAGACAAGGATGTCCTCGCCAGTCAGTTTATCGAAATCAATATTCAGGCTCTCAATAGTATTGCCTTCAAATGTAACCGGTCGGGCAAAAGTATATAGTTCCGCCACAACCTCCCCTATACTGCTCTCTGTTTCCATTGCTCATCTCTCCTTATAGGCCCAGATTGGCCTTGGTGGTAGCAAGATAGTCTACATCATTTACTTTATGAATATAGTTGTATTTATCGATTTCCAGCACTTCAATGCCATCCAACGACACTTTCAAATAATTCACTGAAAAGTTATTGGTGGTATCCATCACTGCGGCGGTATCGAGGTTTCCGAGCGTTAAGCCAAGTGGTCTTGCACGGACCGTAACCTTGAACGGTACCTCACGGTATTCACTCGTTGCCGTGTCAAATGTCTGAATCGAAGCCCGAAGGTCCAGCGTATGAACCTTTGGTGCTAAGAGCGCAGCTGCCGCCTTTTCAATCGTACGCCACTTAAGCGCCAAACTCATCGCTCCCGTATGGCCTGGGGAAGGGGCGGCCATTTCACCCGCGATTCCTCCCCCTTTAACTGTGTCCACCAGGTAAGTAATTTCCGGCAATGTGGCAGTTGCCGTACCCAAGTAATCTGTAGCGTTCAAGTACACCGAATAATCAATAACTCTTTCTGATCTTTTAGTCATATTTCTCCTCCTTTTACGCTACCAGCGCAGCTAAGTATGTTGTGTCGTATTCAAGCAGGAATGAAATCTCTTGTGCCGGTCCAGGCGGTGTGATGTGTAAATGGAATGTAATCTTGCCGGCCATCAATTCCGTTACCGGATTTTCAGACTCATTAAAATCTACCCGTGCTCCCAACAGCGCACCGGATGCAACCAGGCCATTAAGCCAAATATTTACCGAATCCGTAACCGCTGCAATAAGTCGCTTATTCATTGGATCATCAACCTTTTGCATATAGGTCATAATCAGACTATTCCCGATCCAGTTAAACATGCGGCGAACCGGAATGAAGCTGTCTTTGGGGTCCGTTACCCCCGGATAAGCCCCTGTGTTGTTCCCCCAAGACTTCCAGCCGCTCGTTCCAAGATTAACTGCTGTTACAATCCCTGAACTGTTAAGGAAGCTTGCCTGGTCAATCCCTAAAAACAGACTTGTCCCGTCGGAAAGAGTGGTACCATCTGCTTGCAAAGTTTTGTTAGATGGCGATACAAAAGGAACTCCACCGTTATTGGCATCGGTTGCGGCGATAAGTCCTGCGAGTTGCGTAGAGAAATGGTATTGCTTATCCCCCAAGGTCAGCATAGGGTAAGCTGCAATCTGGAGAGGACTGGTATAGCTGTTATCCGACTTCCATGAGCCAGCCGCCGTATAAAGCTGAGCAGGATCAATATCTGTCAAAGCCATTGCCTTGAAGTTGCCATTGATATTTCCCGCTTTTGCCTTCATAACCGCAGCGATTGCAGGTAAATGCGACCACCCCGGAGCCAACAGTATATCAGGAAGAACGCCAAAACGAGGGTAGGCTTGATTTACTAGTTCAAAACCGGTATATTCACCGGACTGCGTCACGCCTCCAATTACATCATCAGCCTCCACTGCATCCGGATCCAGTTTGTTATAACCAATGGACAACTGGCTCACATTTGCCGCTATAGCACCAGTTGACTTCGTTGTTATAATGACATGCCCATTATCATCAAAAGCAGCAGTATAATCGGTGCCTGGCACATAAGCCGATGCTCCGTCTGAAGATTTGACAAGGAGCGTTGACAGCAGAACCCCCTCTGCCTGCAGGATAGCCACTCGGTTACTGACAGCAACCACAGCAGGTGTGACTGTCGTCTTATGTGTAGCGGGGTCAAGCACATTCACCAGTATCAATGGAGCTTTTTCATACAAGGCAAAATGAGAGTAAATTAATTCGCTCAGCGTATAATGTGACCAGTCATCACTATACCCTAGTGCAGCCACCGCTTCCGCGTAAGTATATGCGAGTACTGGAGTGTTCACTGGCACGGCCGCAGTAGCCAAATTAACGGGGGATGTCCCTACTGCAAAAGGAATACCACTTGTTGCCTTTGTCGGTGCCAGAACCGATGTGGATTGTTCAATAATAGTTACACCATGTTTAGAAGCCATTGATTAAATCCCCTTTCCTAAAAGCCTTTGATAAACTACATATTCAGCTGTTCCGGTTTGAACAATACGGTCTTGTACAGCCGTTATTTCTGCTATCGGTACAATCAACTCAGACACATCCGGCTTTTCAGCCAACAGTGGCTGCAAATAAGATGGAATACCGGATCGGAAAACGGTGGATTGTAGCAGTTGTCCACCTGGCAGGTTTGGTCCCAGATAGATTAAGACCTGTTTTTGTTTCTCTTCTTCAAGACCAACCATAGTTTTCAAGGTTTGATTTGGAATCACCTGTACCATATCAGCTTCCACCTGCTCATTCTGATGCTTGTCCTTATTTATATTTCGGCTCACAATTGTACCTCCTGTCTAATTTGGGGCAATGCCCAGGTAGTTGTTAGTTCTCCACCCCATTCGGATGAAGAATGCTCCTCGTTCATTTTCCATTTCCAGCTACCATCCATAGCAAATTTCTGCTCAAGGACTCGCTGACGTAAAAGTAATATGCGTACCCGATCCATCAAATTAAGCAGATCGATTAAACCTGTACTATCCTCGGACTGTGTTCCAAAAAACAGCTTGACTTGAATCTCATCTTTGCTGGTGGCTCCTTCGCCTTCCGCTGGCAGAATCATAATTACTGGGTACCCCGCGCTACTGGCAGTACTCTGATTCAAATAACCCAGAAGCACTGTTGGTATAGGCAGCATGTCATCAGCTAATTCCTTCTCCAGGAATTTTTTTATAGCCATGATCAATAAAGTAATTGTCACATTTCCCCTCCTAGCAGTTAGAATCTTTTTTCAAAACAGCAGAACACAATTTTCCATTTTATCATCTTTTCTACACCTCCTTTGCTGGCGTTATTGTCAGCTCAAAGCTTTTATTTGTCTTTGCATCTATTGAGGGCTTTCACTAGACAATTAATCCATTTTATATTAATAATTCCTTTTATGGCACATTAATTCTTCCCGTTCATTATCGAGCAGATTTTTCTTTGCGCCCGCTGGATATATTCACTTACACTGCCTGCCGAAATCGTGAGCATCTCAGCGATGGCAACATGCGAAAACCCCTCTCCGTTAGCCAGCATGTAGCACTCCCGTTCCCTTTTGCTTAACAGTGCCATTATATATTCCAGTCGTAACTGCTGATCCTCTGAGAGGCCTTCTGAGTTGACCGCATTAGTATGAGTATGTCTGGTGAAAATTTGCATACGCATTGGTTCTAAAAGAATTTCCCGCTCGTAACCGGCTCTCCGTTCTATACCCCTCTTGTTCCCCGGCTGCCGACCAGTGCTCAGCCACTCTACAACATATTCGCAGTCACTGATCATACCAGCGATTACCTTTTTATCATCCGCATCAGCATGCCTATATAATTGTTCTGCTCCCCTCAAGGAAATTTGATAATCTGGAAGCATGTCATCTACAAATTCCGAATATGAAAATAACGGCCGATCTACATACATATTGTTCATGCTCATTCCCCCAATAATTATGAAATACACTCAATAATACGCAATTTCGTATTTTGAATTCATGATATGCTCAATATCGTATATTGTCAACTCAAAATGCACTTAATAATACGATAATGCATATTTACTTTGAGAACCAAAAGCACTAAAATGATATTAACAATACGAAGTAGCGTGTTACTTTGATGTTTTTGAGGAGGAGTATTTGTGCAGAGGGCTGAAGTCTTAAAGAAGTTAATCGAGGAAACAGGCCTGAACACGAAAGCTTTTGCAGAAAAGGCGGGCCTTCCCTATACTACTCTTAGATCAATCTTAATGCGGGGAGTAGGGGGCGCATCTGTCGATAATGTAATTAAGGTTTGCCGTGCTTTGGGTATAACTGCCGAAGATATGGAGCGTTTGGCTTCCGGAACGAACCAAGAAGCTGTAACTCCAATGCTGTCTGAACTTTCTGAATTTGAGGCTTTCCTAAATAATCCGGAGCATGGGCTTTTTTTTAAAGATTATTTGGAGGCTCCTGAAGAACGCAAACGGGAAATGTTAACCTTTTGGCAATTCATCAAGGATTTAGAGAAGAAAAAATCGGAGTTTCCAGGTGAGAAATAAATTATTTTGCGTAAAATCGTGGTTTCAGCCAACGAGCTGATTCCTCATACCCAATATACGAACATACATTCCCATCATGGAGGTTTTTTATGTTTATACATTATAAAAAAACACATCTGGAGCATTTTGTGGAACAAATTTACATAGACCATCACATTCAAATTCCGGAAGATATCACGATTGAAAAACTCTCTACAGAGCTGAATATCTACGTAGAGTACGCACCTATCAGGAGTAGAGCCTATGAATCCAATTCGGGTATACGCTGCATACTTTTGGATAATCGAATAACACCAATGAAGCAACGCTTCGAATTTTTGCATGAGCTCTGTCACATACTGCGACACGCAGGCAATCAAATGGTCCTTCCTAGCCCCTTTATTAAAGCCCAGGAGGAAGATGCAGAGAAATTTCTTCTTTATGCAACTATGCCTTTTTTTATGATTCAACCAGGTGCATTATCTGATGAATATGACGTTGCTATCCATCAGCTTTCCAGTATCTTTGGTGTATCCAAAGATATGGCTAAAAAACGTTTCGATCAAATCCTGCGCCGCGAGTATGAAGGAGAACTTATACCTGATGCTGGTGGTCGACAATTATCAAGGAGAAAGAATGCTGAGCCTAATCAAGATAATTATGAGACTAAAATATTTGCTTATTACGATCCTCACAGCACTTTAGATGGACCGGACCAACTTATCGTTTGTCTTGATCAGAAGACTCTGTTAAGCCAACATGAATGGGTAGTCCCTGTCGAAGAACGGTTTCAAGAGATTGACCTCGAATCATTGAAGAATATTGAAATCGAGTCCGCAACAAGAGGCGATTTGATCTGCTTTGATGGACAATTAACCTTACAAATTCACCAGCTTGTCTACAAATATGGTTTATCAAAACGAAACTTTGTGCTGCAAATGAGGGATATTGAACAGATCCTTGAGGCAGACCAGAGCTCCGTTAGAAAGTTTCTATGATAAAAGATAGGACTACAAAATTAACAAAGCCTCTGGCCCTTTGGGCCAGAGGCTTGATATGCAAGAGATCTTAACGTTTCGAGAACTGAGGCGCACGACGTGCAGCCTTGAGGCCATATTTCTTACGTTCCTTCATGCGTGGGTCACGAGTCAGGAATCCGGCTTTCTTCAAAGATCCACGGTATTCAGGATCAACTTTCAGCAAAGCACGGGCGATCCCGTGACGGATTGCTCCGGCTTGACCCGAAATCCCGCCACCGTGAGCAAGAACGATTACATCGTAGTTGCCCAGTGTTTCAGTCAGGTTCAAAGGTTGTTTTACGATCATCTTCAATGTTTCCACACCGAAATATTCGTCCATCTCACGTTTGTTAATGACAATGCGTCCTTCACCCGGTACAAGGCGAACACGTGCTACCGAATGTTTACGACGACCTGTCCCATAGTATTGTACTTGTGCCATGAAACTGTCCTCCTCTATTCTTATCCGCGAAGTTCGTAAACTTCAGGTTTTTGTGCTGCATGTGGATGCTCGGCGCCTGCATATACTTTGAGTCTCAGCTTCATGTGATCCCCTTGGCGAGTCTTAGGAATCATGCCGTGTACGGCAGATTCAATGACACGTTCCGGTTTGGTCTTCAGCAGGTCCTCAGCAACAGTAACTTTCAAGCCGCCTGGGTGCATCGAGTGACGGTAGTATTTCTTATTTTGCAATTTCTTGCCGGTCAGGTGAATCTTCTCAGCGTTGATAACAATTACGAAATCTCCCGTATCAACATGTGGAGTGAATTGCGGTTTGTGTTTGCCACGGATCAAAGCAGCGGCTTCGCTGGCCAAACGACCAAGTGTTTTGCCTTCGGCATCAATAATGTGCCAATTGCGTTCAACTTCGTTCGGCTTCGCCATATAGGTGGTACGCATGAATGTTTCCTCCTTGTTCTCGTACGAAAATCATCTGTTTCGTATATCTAAGTTCTCATTAAATTACGATTATGTGAGTTAAAAAAAGCTTGGTTTTGGCATTTCCTTGATCGGGGCTGTGGGATAGCCATCAAGAAAACACAACTTTTATATTACAGCATAAACATAACAAGCGCAAGTGATTTCTAATTTTCAATGCATATTTTTTTATAAAAATAAATGCGTTGAACCCTATAGCCCTGCCTCGTCATATTCCACGCTCCACAGTGCCAATCCCTGAGCTACAGCCGTAGGCCCCGCTGCCGCACGGTCACAGGCTGCAAGAATATCCGCAACCGCCTCCGCACGGATTTTGCCTTCACCCACATGTATCAGCGTTCCCATTATAATGCGGACCATATGCTGCAGAAAGCCGCTGCCCGTAATATAAGTGTCAATCACTCCCTGATCAGCAGTCCCGTTCCGGCACATACTACGGTCAACCTCCATATGAGCCTCAAAAATCGTCCGGACATGAGAAGTCTTTGTAGACTTTCTGGACGCGAACGACGTGAAATCATGGGTACCAATGATATGGGCCAAACCTTGCTGCATTGCCGGAAGGTCCAGCTTCACCGGATGATGATACTGCAGGCGCCGTTGAAAAGGGTCCGGGAACCGGTTGCCGTTAATCGTGTAACGGTAAGTTTTGCGCTTAGCCCCTCTGCGGGAGTGGAACTCAAGCGGGACCTCCCGTGCCTCAGTGACTACGATATCCTGCGGCAGCCGGGCATTAAGCGCCAGACACCACCGCTCAAGCGGGATTTTAGAAGCAGTCAGGAAATTGAACGGCTGGCCATAGGCATGCACCCCTGCATCTGTCCGTCCTGAGCCCGTAATCTTAAGCGTCTCGCCGGTTAGATGGAGAATGGCATGTTCCAGATGGTCTTGAATCGTATTGCCCTGAGGCTGGGTCTGAAAGCCATCATAGCGGGTGCCGTCATAATTGACCTTCATCAACAGATTACGCAT

Protein sequences of DBSCAN-SWA_6

>NZ_LN831776|7070941:7123388|7073371_7073908_-|WP_081487084.1|DBSCAN-SWA
MAWIQPTLKLCELHKKNGDDEMILSLAIEQLFPTAEPNKDFEVWDNGPEPILRPGAEEKGRVRYEIKPPKEGEKPAEDVHYRYGIDYNLLTEGEDYDIVERGPYIAVWNLDKPQPTEAELQAAWEAYQEAEANKPPELTGLEQLQKENLLLKSQNNALSERADFIEDIIAEMAMRVYQ
>NZ_LN831776|7070941:7123388|7112932_7115932_-|WP_020427039.1|DBSCAN-SWA
MAGTSSLSSSIYEIVFRLNALVTPAFRQSVEEAEHQVQGLDQALQEMVRRGYFDTLRREVEQADDSIADAGGNVEGFGDKLKNAVKEIDFSMLNKAVEPLKAVWTAVNESSEAMAQLQAETGMSSKEMKEMKEISNNLYSQNYGKNFEDIGNAVGAVKQVLQQTGDELEKTTQTAMTYRDVFKEDITGSLQAVDSMMQKFGISSEQAYNLMAQGAQKGLNTSGGLLNAIEKYSVDFKKMGYSADEMFELLSAGMENGASSLDGVADTVKVFGTTIKNGSDSTKAAIYELFAPEQLKKFSAALVSGGTKSKEFAQLVKVAGKASAAALVGDLKSGGDSANKAMLQLQKTLGTGDTIFKGLADGSMTGKEAMEQVILKLKGIKEPIHQAKLAGSLFGSQFEDMGNKAVLALGQTRNEFDMTRQTLEEAAEIKDSTLSEQFAAMGRELQANLVIPLTESLMPALQGLTSWVSNNKESLMVIGLTVPAAVLATKTVKIVQEFSKIVTAARGASGAAGGIASALGLLTNPVGIAVAGVGLLTAGVIAYKKHQEDARRELLNMGDVLDKAYSNYAEIDHASKRTQNLITEYDRLTQKIKNAKTPADELAEARRKQQLVEQELIEMNPDILSAEGSKNSKFREQLGLVGDIKKAHEQMSRREMEHDALSAQAKLPDLESRYSELTKNLSTQNSDYEKSKVSFRDYHLYMNQLDEIMGGQGNDEQKQQQVDEVLQNLNKAQGTDYGGYAGIAVATVRQDYEKIQGSFDKYYTKIKKTQSEMTEAENSFSSYYDLQKRMIELDLGGTLEQQAKKYKDMSAAQQKQFNQAMSYMVNLNAEVDKLPAEKKVNLQLIWEQTGQIPNFRLSDDEWNDVQAMIKTKGKPDSQTKAGQKAIYWALHDPDFEGYAEGGIANVPSIFGEAGPEIAIPLNGKQRSRSLLEKANDLMGYGDGFSGKGDIHVTWAPNVSLQGGDKSMVEQLREALKQTEDSFERRFKAMVQQQRRVSFQ
>NZ_LN831776|7070941:7123388|7104779_7104914_-|WP_020427030.1|DBSCAN-SWA
MNWYALVKRYFDAGLYTGEQLQVFVTTKKITDKQAKEITKATAV
>NZ_LN831776|7070941:7123388|7122608_7123388_-|WP_020427050.1|tRNA|DBSCAN-SWA
MRNLLMKVNYDGTRYDGFQTQPQGNTIQDHLEHAILHLTGETLKITGSGRTDAGVHAYGQPFNFLTASKIPLERWCLALNARLPQDIVVTEAREVPLEFHSRRGAKRKTYRYTINGNRFPDPFQRRLQYHHPVKLDLPAMQQGLAHIIGTHDFTSFASRKSTKTSHVRTIFEAHMEVDRSMCRNGTADQGVIDTYITGSGFLQHMVRIIMGTLIHVGEGKIRAEAVADILAACDRAAAGPTAVAQGLALWSVEYDEAGL
>NZ_LN831776|7070941:7123388|7110800_7111199_-|WP_039786568.1|tail|DBSCAN-SWA
MNKIGSLGPVIFVVAEGAIRTIDEFKRSSSSRWAQHDIIGKKPKKEFIGPGSDSVSFSVRFSAALGLNPRKELDKLTELDRAGKALPLIIGRKYVGVGLWVITGLSQDWNTLDSIGNVLDAQVTISLEEYVK
>NZ_LN831776|7070941:7123388|7084465_7085788_-|WP_020426176.1|DBSCAN-SWA
MAGGTWTTQNKVRPGVYVNVASNQSAIGKMGTRGITALALSLSWGAPGVITKITAQEDFEKLLGYDLGHPTLLPVREALKRASTVLLYRLNEGVKATVTNNGLQVTAKYGGERGNDISVIIEKNIENNVLFDVKTLLAGTELDKQTVGDADELAANDYVTFQKNGTEGLTLTAGIRLAGGAGGTVTNAAHSDFLGALEVQEFQTVGLLSKDNSLKALYSAFVKRLRDMEGKKVQAVVSDYAAAGHEGIISVKNGVVLSDGTTIDGEHAVAWVAGASAAAAVNESLTYQAYDDAVDADVRLSHSETTDALLNGEFLFTYSGGRAVVEQDINTFTAYAPDKGRAFSKNRVLRVLDGIANDLKSIFEKYYIGKVANNEDGRTMFWSQCATYMNDLQNIGAIEDFKAQTDVVVAAGTDSDSIVVDVAVKPVDSVEKVYMKVKVV
>NZ_LN831776|7070941:7123388|7116081_7116405_-|WP_020427040.1|tail|DBSCAN-SWA
METESSIGEVVAELYTFARPVTFEGNTIESLNIDFDKLTGEDILVCDRQYQAEAARQSSGELIKETNKAYQAYIVAKAAGVHVGLIRALSAKDFTKLTLRAQSFLLL
>NZ_LN831776|7070941:7123388|7080616_7081318_-|WP_020426180.1|DBSCAN-SWA
MEEYGFFLSFNELEDLFRLPVNPETLEIKESGDSKSYTIVDLGEINAIAYPKLTEITIESIFPAQHYPFVLVRSEGPNRLLRPFEYVEMIQKWMKSRRPIRFVLSGVNLKGEQDHSAVPNDLALNMAMSIESFTWKLSAGTSGDVEYSLSLKKYVFYQASPVKIVKGQVKAEPKRASDKAVPKTYTMKAGDSLWSIAKKILGDGQKYKVIQKLNGIKDSELKKLPIGKVLKLP
>NZ_LN831776|7070941:7123388|7098015_7098837_-|WP_020427023.1|DBSCAN-SWA
MNIKRYMIKDTNESVLKKLDPDESGDFKSKEEAEAKTAKLKERLAELQDILFAQKKHSLLVILQGMDSSGKDGTVKHIFSGINPQGFMVTSFKKPSLEEEAHDFLWRVHMKTPPKGYIAAFNRSHYEDVLVPRVHGTLKKEERKRRFRYIREFEAMLAEEGTTIIKLFLHISKDKQLEKIQERLQDPAKHWKFDASDLQERQYWDDYQAAYDDVFKETSTDTAPWYWIPANHRWYRNYLALAIVVKTLEGLDLSYPKLDTPTPDISQLISPRH
>NZ_LN831776|7070941:7123388|7097160_7097964_+|WP_039832611.1|DBSCAN-SWA
MNSFYVFSGKKIKRFIYIFAAALLAAGVVYVERGNITVFSETAPSAIYSVPTEKKLIALTFDISWGEKRPGPILKVLEDKKVDKATFFLSSPWSKTHQEIVTSIKDAGYEIGSHGHKHVNYSALSNEEIKNQITTAHTVLTELTGKEPNLIRMPNGDFDKRVLQVATDLGYKVIQWDTDSLDWKNIGVDNIVRRVTSKAHPGDIVLLHASDSCKQTHEALPQIIDNLRSQGYEFVTVSELISQGSAEGKEVRDSAMLNDGLEDAAGM
>NZ_LN831776|7070941:7123388|7076418_7077441_-|WP_020426186.1|DBSCAN-SWA
MAQTIQVKRGTRAELAAYGVLQAGEMGFCTDTKEVYIGDGTSNSMVGRAMSGPEASRPAAASAGRVYIVTSGTNSGYLYFDDGAAWRRINVQKLSDLTGSVDEVADGATYAKVLKADITAGHINKISDGTNIKTAAEIKTHIDDASKHRVINDAGTAITDLWSAQKIRNEIELAKHNIEPQSSVKDQNLAVPPASPAEGDRYIIPAAATGVWAGKTSQIAEYQSAAWVYYTPAVGWTAYVDDEQKIYSWNGSAWVRTGGALQTITAGNGLTGGGQADSVTLNIGAGYGIGVTADAIAVTAGKGITVDANGVAANVDGSSIVYDTVNGNRLMVGAIDGGTF
>NZ_LN831776|7070941:7123388|7103702_7104395_-|WP_020427029.1|DBSCAN-SWA
MNLLEKEDLIRVKAEELEHATPEEIIRWAVETFPNITFACSFGAEDVVLVDMLQKVSPSTDVFYLDTDFHFKETYETRDIMADKYGMEFVRVSPQITPAEQAVQYGEALWSTDPNQCCAIRKVEPLTRILSQYDAWITGIRRDQAPTRANAKKVEYDNKFGLVKFNPIANWTSEDVWSYIRENDVVYNPLHDRNFPSIGCEQCTRAVMPGEDPRAGRWSGSDKTECGLHK
>NZ_LN831776|7070941:7123388|7086860_7087379_-|WP_085981499.1|DBSCAN-SWA
MMNLSSLPELDRRRTQTTIESMLEKYRIFKTVTFEAKEAGITYSYSERFHGPTHTITDQTATIAAHNVDVPAARRAYCAALDSVVDRLDKREQQLVRERYMRRDEVYDYTVYNHVFDPPVSKDTYVKIRSKAFYKMALALTDLGLLSLDSLMKNGSSMKQEELKSRRLPSVY
>NZ_LN831776|7070941:7123388|7083468_7083891_-|WP_020426178.1|portal|DBSCAN-SWA
MSELSMFFAQNVACDTTEEFVVSQRFKDKEGQPVAWKLRSMTEDENQECRKAATRKVKGKSGVYTSEIDPNDYMAKLMTSSVVHPDLKNAELQRSYNVLGAEALLRKMLLPGEFAALGERVQALNGFATDMNELVEEVKN
>NZ_LN831776|7070941:7123388|7118399_7118747_-|WP_020427043.1|DBSCAN-SWA
MSRNINKDKHQNEQVEADMVQVIPNQTLKTMVGLEEEKQKQVLIYLGPNLPGGQLLQSTVFRSGIPSYLQPLLAEKPDVSELIVPIAEITAVQDRIVQTGTAEYVVYQRLLGKGI
>NZ_LN831776|7070941:7123388|7119354_7119816_-|WP_039786575.1|DBSCAN-SWA
MLPDYQISLRGAEQLYRHADADDKKVIAGMISDCEYVVEWLSTGRQPGNKRGIERRAGYEREILLEPMRMQIFTRHTHTNAVNSEGLSEDQQLRLEYIMALLSKRERECYMLANGEGFSHVAIAEMLTISAGSVSEYIQRAQRKICSIMNGKN
>NZ_LN831776|7070941:7123388|7121526_7121919_-|WP_020427048.1|DBSCAN-SWA
MAQVQYYGTGRRKHSVARVRLVPGEGRIVINKREMDEYFGVETLKMIVKQPLNLTETLGNYDVIVLAHGGGISGQAGAIRHGIARALLKVDPEYRGSLKKAGFLTRDPRMKERKKYGLKAARRAPQFSKR
>NZ_LN831776|7070941:7123388|7071326_7072025_-|WP_039785526.1|DBSCAN-SWA
MLTLTQIKNKSAPRLIGLHPVVLAAVGALIERCYACGVPILITQGLRTAAEQDALYAQGRTKSGAIVTNARGGQSYHNYGLAVDFALLLPNGSSVSWDMARDGDNDQAADWLEVVQQAKRLGFEWGGDWTSLKDYPHFQMSFGLTLSKLRAGAQPSVQAVEAAYKLINGRTKEEQNLNSDVITIVKVNGAKIADGRLEHGVTYVPVRAVAEALGASVGYDPVTRTVEITSGR
>NZ_LN831776|7070941:7123388|7104914_7105253_-|WP_020427031.1|DBSCAN-SWA
MNMFDAMVYLYPDLEPKKDFQIWDDSDGKGPYIGVWETDTPKPTTEELQRAWEELQAQPVPELPETDAERMARLEAENATLLLELVQTQTRQNQVEKDQAALLLSLVEGGVL
>NZ_LN831776|7070941:7123388|7120080_7120479_+|WP_020427046.1|DBSCAN-SWA
MQRAEVLKKLIEETGLNTKAFAEKAGLPYTTLRSILMRGVGGASVDNVIKVCRALGITAEDMERLASGTNQEAVTPMLSELSEFEAFLNNPEHGLFFKDYLEAPEERKREMLTFWQFIKDLEKKKSEFPGEK
>NZ_LN831776|7070941:7123388|7079339_7079636_-|WP_020426182.1|DBSCAN-SWA
MLDIIKKASLGAVGSTNPVAFSYGTVTVAAPLQIQVDQRFILSGAALVLPESVMESKLEWDGREIVLRRGLEKGDRVLMVRMQGGQSYVVLDRLVDPI
>NZ_LN831776|7070941:7123388|7121939_7122377_-|WP_020427049.1|DBSCAN-SWA
MRTTYMAKPNEVERNWHIIDAEGKTLGRLASEAAALIRGKHKPQFTPHVDTGDFVIVINAEKIHLTGKKLQNKKYYRHSMHPGGLKVTVAEDLLKTKPERVIESAVHGMIPKTRQGDHMKLRLKVYAGAEHPHAAQKPEVYELRG
>NZ_LN831776|7070941:7123388|7083999_7084464_-|WP_020426177.1|tail|DBSCAN-SWA
MAFLKASDTLSGQEGRAYAVIGTQTEEMFYVKTLEATVEKTKAEVKTLGRRGVQHKATGWSGSGTMTIFYMTSRFRQMMLDYMHTGVDQYFDIEVTNDDPSSSVGAQRIILKGVNLDSVIMASLDTESDALEEEVSFTFEDVQIAQAFGSPALQ
>NZ_LN831776|7070941:7123388|7077860_7078919_-|WP_020426184.1|plate|DBSCAN-SWA
MYEDQTFEALLGRMLDRVPSSLDKREGSIIYDALAPAAAEMAQMYIELDVNSNLFFADTATGEYLERSIAWSGITRRAASKAELKAMFYNSASGLLDVPLGSRFSLDLLHYTAVEKLAPGTYRLESETAGEEGNRYFGSLLPIDYIPVLARGEITALLIPGENAEDDEALRQRYLESVRRPSTSGNKYHYMEWALQIDGVGGARVFPLWNGPKTVKVVIVDAAKRPASELLVSQVQQYIDPVSGQGEGQAPVGAVVTVAAAAGKSISVSAKVTLASGYSLQEVIDAFKEILEKYRKEKAFTASYISQSVIGSLLLDTEGVVDYSGLKLNGVTGNVTLSETEVPLFSSVVLEV
>NZ_LN831776|7070941:7123388|7071996_7072389_-|WP_020426194.1|DBSCAN-SWA
MGVIDVLLLIAYSMSLICALLLIAALFLYFRRRLRAKAVSLFMVAAFFFLSAYTVQMAIALWIRFTAVPGAGAVLASLQTEALAVAQTGTTIGLLILTLLVFTKRQDLFIVLQEGKKGGASHADPDTNQK
>NZ_LN831776|7070941:7123388|7118743_7119166_-|WP_020427044.1|DBSCAN-SWA
MTITLLIMAIKKFLEKELADDMLPIPTVLLGYLNQSTASSAGYPVIMILPAEGEGATSKDEIQVKLFFGTQSEDSTGLIDLLNLMDRVRILLLRQRVLEQKFAMDGSWKWKMNEEHSSSEWGGELTTTWALPQIRQEVQL
>NZ_LN831776|7070941:7123388|7088173_7088587_+|WP_020426170.1|DBSCAN-SWA
MDEIINKLIKKYKTNSPFELSKALGIHIRFMNLGQSTKGLYYRKLRRRFIVIHNELPLEWQRFVCAHELGHDRLHKGINRFFLEENSYFSPGKLERQANLFAIKLLSSGSSPEQEEPLLRYYLRIGIPPEVIFFLDE
>NZ_LN831776|7070941:7123388|7110474_7110804_-|WP_020427035.1|DBSCAN-SWA
MIYTVDMTQPTHINFTPETVEEEVSQNIRTILTTPRGCAPLARGIGLDYTIIDEPASIAESRLIAEVITAITEQEPRASVSEISFKDDIKDSLNGCLAVVVKYTLVEEE
>NZ_LN831776|7070941:7123388|7070941_7071205_-|WP_039785532.1|holin|DBSCAN-SWA
MDNVLAFASVLAVFTLALVQLIKNNINLPRNAVPFIGLGIGLLIGAAAYPFTDLGLTLRLWSGGLAGLSATGLFELAFNDRPGTTQK
>NZ_LN831776|7070941:7123388|7078911_7079343_-|WP_020426183.1|DBSCAN-SWA
MIPVIGNAGPITAPLEGDTSLGNTEMSSLTYRMDWDKKRITSRLDGLEAVQQAVAKMLRTDRYEHLIYSSDYGTEWSLVLGKDRLLVRAEIRRIVSEALLQDERIIGLEDTKVSFNGDNLSFSCKVITQYGNFELRKEMSEGV
>NZ_LN831776|7070941:7123388|7085960_7086374_-|WP_141639041.1|DBSCAN-SWA
MSVQQLRNQINAALGRYFPDLPVYVSGEKPRGAYFEPGLISATLDRQREGRYLAVYRFGIRYEQGSRLNAENMADGLSEALASMEREGEAFRVIRQAWEAGTEGKGPLFTADFMIYLQTAAVERVPMRHMTGGERLK
>NZ_LN831776|7070941:7123388|7111696_7112719_-|WP_039786570.1|DBSCAN-SWA
MQDARRAVLELKYNGKDITMDIAKSLTDFQYNDAVSGSLDDLTVSLEDRERNWQGPWVPVEGDQINASIRTINWDKPGENKKLPLGTFEIDSIDFNGPPDTISIKAVSLPISSEIRMQRSSRSWEKTNLKTVAAQVAKRANLKLIYEAQDNPSYERLEQSEMSDLAFLLNTATQEGIAIKVSGGSLILFDEMVYEQKEAITTIVRGDDNVTGYSFALNTAYAAFRACTVTYTPPTSKEPLKATYTPNGAPKNGPVLKINEQVDTKADALRLARKRLRERNKEGGKGTLSLMGDIRMVTGLTINIKGWQRFDGKYIIESAKHSIGSSGYTTNLEIRKVLGW
>NZ_LN831776|7070941:7123388|7087686_7088136_+|WP_020426171.1|DBSCAN-SWA
MAEEFGNYLRQLREQKGLTINQLASLAGISGAQISRIENGRRGVPKPATLRKIAEAADVPYEELMEHAGYLSEDMQSGAEDKVPEWATSKDKRDFRKMLEDDGELMFDGIPLNKEDKQRIKDVLTGLFWDAKQMNKRTIPKHDSSGGKS
>NZ_LN831776|7070941:7123388|7120568_7121456_+|WP_020427047.1|DBSCAN-SWA
MFIHYKKTHLEHFVEQIYIDHHIQIPEDITIEKLSTELNIYVEYAPIRSRAYESNSGIRCILLDNRITPMKQRFEFLHELCHILRHAGNQMVLPSPFIKAQEEDAEKFLLYATMPFFMIQPGALSDEYDVAIHQLSSIFGVSKDMAKKRFDQILRREYEGELIPDAGGRQLSRRKNAEPNQDNYETKIFAYYDPHSTLDGPDQLIVCLDQKTLLSQHEWVVPVEERFQEIDLESLKNIEIESATRGDLICFDGQLTLQIHQLVYKYGLSKRNFVLQMRDIEQILEADQSSVRKFL
>NZ_LN831776|7070941:7123388|7076070_7076406_-|WP_020426187.1|DBSCAN-SWA
MALKTLIQIRRGQESALGTLAVGELGFCTDTGKLYIGTGTVNKLLVASQSTGDMLKSIYDTNNNGKVDYAQAADTVPWSGVDGKPAVYPPAAHTHEYMPKGPLSWNQLKGV
>NZ_LN831776|7070941:7123388|7095958_7096189_-|WP_020427019.1|DBSCAN-SWA
MLGMLFNEKECKELDYVLRKELDEMLLDLSDQRLDHNIRHAIANRYKTVFRMYARFAPQKELSKYAWGGRYSQSKH
>NZ_LN831776|7070941:7123388|7072574_7072883_-|WP_020426192.1|DBSCAN-SWA
MNSNDVANLEKILPLADKYGLAYIVALILLVIVLVLLRSIVKGNLVPRELLERAEEDRDRLQNILDKERSDFMAPTLEVLQRLKVDYTSSGVNVVNEEDRGG
>NZ_LN831776|7070941:7123388|7099729_7100425_+|WP_020427025.1|DBSCAN-SWA
MKWRTLWTGSLVLSMVMALTACGSEQSGSSSGQVSYKEMKTMVVDILKSEEGKKAVEEAMSTPSSGTEGTSTSGLSMKMMPLQTTEQIRVAVKDTITAPEYQKEIEKIMTDPKFAGDFAKAVNSQSKELHLQLIKDPTYQKSVAEIMKSPEMMKMFLDLTKTSDYRKQSMTIMQEAMQNPLFRMEVLDLLKTVVQDELQPKVEKGGEGKEGQGKGQGQGGKSKQGGDDSGS
>NZ_LN831776|7070941:7123388|7077442_7077856_-|WP_020426185.1|DBSCAN-SWA
MGYPQQIDEFTDKLNKKANGGSYVVEEKLFLTDGVYSGLLAHDNINNQSIAVYTGSRYSGVELRNFSVSFPDETPWRRMIKIFAEVPEVYVTYETPGDTVEADDINVLQWGLTAAQRELERYKATGRIDGGSFRREV
>NZ_LN831776|7070941:7123388|7108799_7109351_-|WP_020427033.1|tail|DBSCAN-SWA
MINIQTVSLLDLMPPSIRNDSAMAAAAIALDTQLQGITNMIAALDIFGRSAEWTDAETDELAWQYNPPYYDPDLPLDQKRLLIKNAIAFHRHKGTAGAVEDLIAILFGEGAVEEWWQYGGDPYHFRVVTNNADVTTIRAQEFVSAVDAVKRLSAVLDSVTISQAEELPLYFGGFLHFGETITI
>NZ_LN831776|7070941:7123388|7116950_7118396_-|WP_020427042.1|tail|DBSCAN-SWA
MASKHGVTIIEQSTSVLAPTKATSGIPFAVGTSPVNLATAAVPVNTPVLAYTYAEAVAALGYSDDWSHYTLSELIYSHFALYEKAPLILVNVLDPATHKTTVTPAVVAVSNRVAILQAEGVLLSTLLVKSSDGASAYVPGTDYTAAFDDNGHVIITTKSTGAIAANVSQLSIGYNKLDPDAVEADDVIGGVTQSGEYTGFELVNQAYPRFGVLPDILLAPGWSHLPAIAAVMKAKAGNINGNFKAMALTDIDPAQLYTAAGSWKSDNSYTSPLQIAAYPMLTLGDKQYHFSTQLAGLIAATDANNGGVPFVSPSNKTLQADGTTLSDGTSLFLGIDQASFLNSSGIVTAVNLGTSGWKSWGNNTGAYPGVTDPKDSFIPVRRMFNWIGNSLIMTYMQKVDDPMNKRLIAAVTDSVNIWLNGLVASGALLGARVDFNESENPVTELMAGKITFHLHITPPGPAQEISFLLEYDTTYLAALVA
>NZ_LN831776|7070941:7123388|7096441_7097053_-|WP_020427020.1|DBSCAN-SWA
MLSFPAFARDLSTIRKALLFALLLFVAGGVIGWIGTGSLQKLLSGQLEGLSKISGSLKESAHPQWSFFQFIFLNNSIKGVLIIFLGAIFGILPALFLLINGGVIGYLIHISAMQGMDLFDLIVKGLLPHGIIEIPAIIIACAFGLQFGWNVISDLFSSAAAREKRSGAWPAFMRQTLRASIWIVILLFVAAIIESTITFSLLS
>NZ_LN831776|7070941:7123388|7116418_7116937_-|WP_020427041.1|tail|DBSCAN-SWA
MTKRSERVIDYSVYLNATDYLGTATATLPEITYLVDTVKGGGIAGEMAAPSPGHTGAMSLALKWRTIEKAAAALLAPKVHTLDLRASIQTFDTATSEYREVPFKVTVRARPLGLTLGNLDTAAVMDTTNNFSVNYLKVSLDGIEVLEIDKYNYIHKVNDVDYLATTKANLGL
>NZ_LN831776|7070941:7123388|7079641_7080604_-|WP_020426181.1|DBSCAN-SWA
MELLLKNKEGLLWDIAGIVSDLSWKTSRAGKPATLDMTIIDSGIYQHPKFKISNGDIVQFRKDGINVFYGFVFSIDTGSDQQIKLTAYDQIRYLLGNGSYVLQDVTASELISKIAKDYGLKTGVLEETTYRMPSLIEDDKKLLDIIMRAIGGELEKKGRLMAFYDDFGQLTLRGMDSMKLDLVLGAGHYLYDYSLKKSIDDDTYNTIYLYKDNKESGKREFYPVSDPENVKRWGILHLYKKADDKANAAQIQENADNLLKLHNREKTSLSVQAIGDLRVRAGNLIYVLLDALDTRLFLVEQCSHKISGGEHTMSLDIKVV
>NZ_LN831776|7070941:7123388|7085787_7085964_-|WP_020426175.1|DBSCAN-SWA
MNTNEVSDTAFSTKQIVNSLHFSPGEKDVLNVILLEDQSYTLEEAREQLKSFLNKEVI
>NZ_LN831776|7070941:7123388|7101668_7102415_-|WP_020427027.1|DBSCAN-SWA
MSGRKQGKVSVWISWSSIKKGMLGAVLLAVMIGIIAYDMPTAKTLNYWSLPLSGKVIAIDAGHGGPDGGAVSREGLIEKDINLSVSLYLRDYLQQAGAIVVMTREGDYDLARQDTKGYAKRKTEDLKQRVRSIEEKRADLFVSVHMNSVPSGRWSGAQTFYYPNHTGNKALAGFVQAELKATLENTDRIAKTVNTVYLLKALKMPAVLVEVGFLSHPQESALLGDDVYQRKVATSIYRGILRYASEQP
>NZ_LN831776|7070941:7123388|7100468_7101578_-|WP_020427026.1|DBSCAN-SWA
MLTREQIQELLQPLTDPESGKSLIELQLIRDIMVKEDRISLSLVCLDTDEKSRMELEQKVRDLLTEGGAGNIHIRLRDATDYERSILRGESTEDKPEPEQGGALKGHAAGLEGHELINKDSGVNFIAIASGKGGVGKSTVTVNLAVALARKGKKVGLIDADIYGFSIPDMMGIEEGPIVEEGTIIPVERFGVKVMSMGFFIRENSPVIWRGPMLGKMLRQFFSDVGWGELDYMLLDLPPGTGDVALDVHQMLPHSKEIIVTTPHATAAFVAARAGSMALQTDHEILGVIENMAYYECSSCGKKDYIFGRGGGARLAETLHTELLAQIPLGAPDNHISEPDFSPSVYKAETATAQLFAEIADKLIANNEQ
>NZ_LN831776|7070941:7123388|7083289_7083469_-|WP_081487083.1|DBSCAN-SWA
MNGGDGEANLAYYALHELHILPHELMKLSARERAAIYAMIAVRVEKEKREQSRSKGKRR
>NZ_LN831776|7070941:7123388|7102487_7103663_-|WP_020427028.1|DBSCAN-SWA
MTSILPHGGTLIRRVAEGAHREELLQQASGYKSIPVNTWTLSDLDLIGVGAFSPLTGFLNEEDYHSVVKSMRLADGTVWSIPVTLSVEDEAASGLAVGERVSLIGEEDGVIYGLLDIESIYEADQQFEAQNVFKTTDPAHPGVSKLLARASTYVGGPITVLNRPAPEKFKEFYFDPAQTRQIFADKGWRTVVGFQTRNPVHRAHEYIQKCAMEVVDALFLNPLVGETKSDDVPANVRMKSYLALLENYYPKDRTFLGVFPAAMRYAGPREAIFHAMVRKNYGCTHFIVGRDHAGVGDYYGTYEAQEIFSNFTAEELGITPLFFEHSFFCVKCGNMASSKTCPHPGDQHLTLSGTKVRGLLREGKCPPPEFTRPEVAEILIEGMSVEVTAQS
>NZ_LN831776|7070941:7123388|7109343_7110471_-|WP_020427034.1|plate|DBSCAN-SWA
MEYAELPDILFSEEDAAAIQQDVITVYEGLAGRSLQPADPVRLFLSSLAAIIVQQKVLINQTAKGNLLRYASGAVLDHMGAFQGSERLNASAAIVTLQFVLSIPLASATSIPTGTRVGAQGGNGSIFFSTTEYVEIPAGETAGIATAVCSDPGAIGNGFLPGQINVLMDPLPFVQSVSNLTISSGGAAAETDEAFKERIRNAPESYSTAGPQGAYEFWAKSASSAIIDVHAYSPAEGRVTVVPLLADGEVPSQDVLDSISETLEDRGIRPLTDLVTVSAPQPVSYNTIVTYYISRSRASEVSSIQEKISAAVTAYQRWQKVKLGRHVNPSELISRIMAAGAQRVVPTAPVYTILTATQVAQTGTTTITFGGLVDD
>NZ_LN831776|7070941:7123388|7075456_7076068_-|WP_020426188.1|DBSCAN-SWA
MTYGENLYGTISYSSSPATQDGPEFSKPDLMKYLPEYYQGVLEMEQIQDSHAAECGQLAYSIEDSALQTNVESATWGLARWEKVLALTTDNTKSYAARREMIKAKLRGSGTTTPEMIRRTASAFSGGDVQVVEVPGAYSFEVRFVGTLGIPENMAGLIQIIEEIKPAHLDYKFVYSYTWWNSLKSLTWNAAHARTWNELRVYE
>NZ_LN831776|7070941:7123388|7072375_7072573_-|WP_020426193.1|DBSCAN-SWA
MLSRWIKRLSPLHREKERELTQASARVMFSILRYKDVSKEIQEEIQNNGFAEFLIYDRGVNNGRN
>NZ_LN831776|7070941:7123388|7073864_7075445_-|WP_020426189.1|DBSCAN-SWA
MQTTGNLGLKKPDGTDIVDIADLNGNMDVLDTAVKNVQDHAVDTVKHITAAERTAWNAKASTAAATASAAGLMAAADKAKLDGVAAGANKYVHPNHTGDVTSTGDGVTAIAPGVIVNADINAAAAIDATKIGTGVVSNAEFGYLDGVTSGIQGQLNSKAPLATTPQQTTADITYYVRTDGNDGNNGLANTAGGAFRTIQKAVSMIPDTVNHFVAVNVAAGTYAEIISLSGYSGSGQIAVMGDSVVSTSRTVDAIKMYSNSCFVTVNGFNCLPPSGTNAVSVISSVGALINNINSTVAAGTGAGLDVNLSNIRATSCNFSNKFIAVNAVNASVAYIENFTGSGNTWGNRSVLGSVVTAAGTRVTGTSGDSSDNGILTYGGVINPWGDNTHDIRAIVWCGGLASGLTTTASAWNLLRYVISTNQQSGYNTTTGVFTSPQTGWYKIKAAVQLQSAPAATYQLGILQNGSSRWIADVLTTTVTTHTFLSGDIFLYLPAGQTAAIQLYTDMYSVAIVNGMDTTHLEIVRVA
>NZ_LN831776|7070941:7123388|7112735_7112936_-|WP_081487119.1|tail|DBSCAN-SWA
MIYRTVQGDTWDGIAFKLYGDVQFMTLLLNANPTQADVSIFSGNIVLKVPNLPSELTNSLPPWRRE
>NZ_LN831776|7070941:7123388|7099010_7099601_-|WP_039786559.1|DBSCAN-SWA
MNIKKWFFLFWTTLLIGAGGAVIAGLALQTVNGTIHFKSTADTLIYPLILLGYGMLVSVYAQLGFFAYLILNYMGIGVFPRRVWQYVQVVLAVLALLELIFLRTFVGSGRDVSSDWILGIGILLTALIVAYFKVRSTNLTAWIPTFFFMTAITIVEIIGVLQIGVDSATVFIVIPLVACNAFQILMLHRILKPISA
>NZ_LN831776|7070941:7123388|7111287_7111695_-|WP_020427037.1|plate|DBSCAN-SWA
MILIGRVSTSDAVAGSVRVTFADRDDMVSGELPVITPGGWGRGNAIPLPGERVLCVFLDNGRSAGFCLGTYFAEDDPPSGTKDQRGVWFEDGSYVYYDRTAKRLNIKGTGGMKIEGDLTVTGIVSADVFNTKGGV
>NZ_LN831776|7070941:7123388|7081319_7083269_-|WP_020426179.1|DBSCAN-SWA
MRIDVSKAVMLPVKSLAIWKVLNKQSQRIGVKLDLANRSIKGMQAALTRSSDELNRTLDKVNQSLLDINDTLLEGFKRMPPQILVTRDIVVGQSQQASQSQQLGVRMLNASPTVQAAKKEEEKAKEVEWWKGFEKKEKKEEKEEEKKPEIKVEPLPTPKINLKKEPPVPPVPPTPPQPDSKILNFLKTADWVTPFNKIKSFGEKAVKAAVKPGDIADWNKLNDNVDAAMGKIGVKALGALRPVMDTLNQALTSGQLAPTIDALANGFLVIANVIGMIVDGLLWLVGVVQENWAIIEPILIAIAVVYLAAMIVQVYLLAAAWLAANWPILIVIAVIAGLILIFQNLGISAGQVVGAIAGAFSWLMAVFQNIWIGLQNGFYVVWDGIVNGFNTAVLFVKQLLYGLGMGTLDVLYNMAVGVESFADGFVKVMVEAIRWVVDKFNGMAEALSKIPFFDKMGIGTIKLDLDGLKVPHAASELVDKYRKEFKTLEPPEDITKQETKHKEYVDTKDAFNSSYTQAKEWTDNKVESISSAFSDKGRDAKKLTKPPASGQQIQNTAGLFANQGGNLNNVNRVNEVGSINDTVDISSEDLEMMRELAEIQAIQNFVELTPTVQVTTGNINNAGDIDTIINKIGQKLNEEFVSTAQGVYT

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_039785532.1|7070941_7071205_-|holin	holin	A0A1W6JQK4	Staphylococcus_phage	3.6e-08	41.1
WP_039785526.1|7071326_7072025_-	hypothetical protein	A0A127AWA8	Bacillus_phage	1.2e-39	55.6
WP_020426194.1|7071996_7072389_-	hypothetical protein	NA	NA	NA	NA
WP_020426193.1|7072375_7072573_-	hypothetical protein	NA	NA	NA	NA
WP_020426192.1|7072574_7072883_-	hypothetical protein	NA	NA	NA	NA
WP_081487084.1|7073371_7073908_-	hypothetical protein	NA	NA	NA	NA
WP_020426189.1|7073864_7075445_-	hypothetical protein	A0A218M356	Acidovorax_phage	7.5e-08	39.2
WP_020426188.1|7075456_7076068_-	YmfQ family protein	S6BFJ0	Thermus_phage	6.6e-45	51.4
WP_020426187.1|7076070_7076406_-	hypothetical protein	A0A0A7S181	Clostridium_phage	5.6e-06	65.7
WP_020426186.1|7076418_7077441_-	DUF2793 domain-containing protein	A0A1X9IAR6	Xanthomonas_phage	1.4e-15	50.0
WP_020426185.1|7077442_7077856_-	hypothetical protein	A0A0A7S1G0	Clostridium_phage	5.1e-33	54.5
WP_020426184.1|7077860_7078919_-|plate	baseplate J/gp47 family protein	S6AVU3	Thermus_phage	2.4e-95	53.7
WP_020426183.1|7078911_7079343_-	DUF2634 domain-containing protein	S6B9X2	Thermus_phage	4.7e-21	43.3
WP_020426182.1|7079339_7079636_-	DUF2577 domain-containing protein	A0A0A7RTJ2	Clostridium_phage	3.4e-15	41.3
WP_020426181.1|7079641_7080604_-	hypothetical protein	S5MNC9	Brevibacillus_phage	3.2e-86	47.2
WP_020426180.1|7080616_7081318_-	LysM peptidoglycan-binding domain-containing protein	S5MUH0	Brevibacillus_phage	2.5e-48	45.1
WP_020426179.1|7081319_7083269_-	hypothetical protein	S5MNW9	Brevibacillus_phage	1.0e-19	28.8
WP_081487083.1|7083289_7083469_-	hypothetical protein	NA	NA	NA	NA
WP_020426178.1|7083468_7083891_-|portal	phage portal protein	A0A0A7RTY8	Clostridium_phage	4.3e-11	38.1
WP_020426177.1|7083999_7084464_-|tail	phage tail tube protein	A0A0K2CNG3	Brevibacillus_phage	3.7e-48	59.5
WP_020426176.1|7084465_7085788_-	hypothetical protein	S5MNC1	Brevibacillus_phage	3.1e-108	48.4
WP_020426175.1|7085787_7085964_-	hypothetical protein	NA	NA	NA	NA
WP_141639041.1|7085960_7086374_-	hypothetical protein	NA	NA	NA	NA
WP_085981499.1|7086860_7087379_-	transcriptional regulator	A0A0C5AFG5	Paenibacillus_phage	1.1e-40	61.2
WP_020426171.1|7087686_7088136_+	helix-turn-helix domain-containing protein	S6C481	Thermus_phage	2.6e-22	45.6
WP_020426170.1|7088173_7088587_+	ImmA/IrrE family metallo-endopeptidase	NA	NA	NA	NA
WP_020427019.1|7095958_7096189_-	hypothetical protein	NA	NA	NA	NA
WP_020427020.1|7096441_7097053_-	hypothetical protein	NA	NA	NA	NA
WP_039832611.1|7097160_7097964_+	polysaccharide deacetylase family sporulation protein PdaB	NA	NA	NA	NA
WP_020427023.1|7098015_7098837_-	hypothetical protein	NA	NA	NA	NA
WP_039786559.1|7099010_7099601_-	KinB signaling pathway activation protein	NA	NA	NA	NA
WP_020427025.1|7099729_7100425_+	hypothetical protein	NA	NA	NA	NA
WP_020427026.1|7100468_7101578_-	Mrp/NBP35 family ATP-binding protein	NA	NA	NA	NA
WP_020427027.1|7101668_7102415_-	N-acetylmuramoyl-L-alanine amidase CwlD	A0A0N9SGH1	Paenibacillus_phage	5.6e-14	34.8
WP_020427028.1|7102487_7103663_-	sulfate adenylyltransferase	A0A2K9L0F0	Tupanvirus	2.9e-49	30.9
WP_020427029.1|7103702_7104395_-	phosphoadenylyl-sulfate reductase	NA	NA	NA	NA
WP_020427030.1|7104779_7104914_-	XkdX family protein	NA	NA	NA	NA
WP_020427031.1|7104914_7105253_-	hypothetical protein	NA	NA	NA	NA
WP_020427033.1|7108799_7109351_-|tail	phage tail protein I	A0A0C5AJ63	Bacteriophage	1.9e-51	55.2
WP_020427034.1|7109343_7110471_-|plate	baseplate J/gp47 family protein	A0A0C5AEG2	Bacteriophage	6.1e-113	57.5
WP_020427035.1|7110474_7110804_-	hypothetical protein	A0A0C5ABJ8	Bacteriophage	2.0e-16	45.8
WP_039786568.1|7110800_7111199_-|tail	phage tail protein	A0A0C5AN08	Bacteriophage	8.3e-33	50.4
WP_020427037.1|7111287_7111695_-|plate	phage baseplate assembly protein V	NA	NA	NA	NA
WP_039786570.1|7111696_7112719_-	phage late control protein	A0A0C5AJ59	Bacteriophage	1.3e-106	53.8
WP_081487119.1|7112735_7112936_-|tail	phage tail protein	NA	NA	NA	NA
WP_020427039.1|7112932_7115932_-	hypothetical protein	M4ZR40	Bacillus_phage	2.1e-19	33.6
WP_020427040.1|7116081_7116405_-|tail	phage tail assembly protein	A0A0C5AEP1	Bacteriophage	2.7e-13	48.4
WP_020427041.1|7116418_7116937_-|tail	phage major tail tube protein	A0A0C5AJ56	Bacteriophage	2.1e-36	45.9
WP_020427042.1|7116950_7118396_-|tail	phage tail sheath family protein	A0A0C5AEE8	Bacteriophage	5.4e-122	46.8
WP_020427043.1|7118399_7118747_-	hypothetical protein	NA	NA	NA	NA
WP_020427044.1|7118743_7119166_-	hypothetical protein	NA	NA	NA	NA
WP_039786575.1|7119354_7119816_-	hypothetical protein	A0A1L2JY33	Aeribacillus_phage	1.4e-26	40.4
WP_020427046.1|7120080_7120479_+	helix-turn-helix transcriptional regulator	R9TNF4	Paenibacillus_phage	1.3e-17	60.3
WP_020427047.1|7120568_7121456_+	ImmA/IrrE family metallo-endopeptidase	A0A2H4JA43	uncultured_Caudovirales_phage	7.4e-13	29.8
WP_020427048.1|7121526_7121919_-	30S ribosomal protein S9	NA	NA	NA	NA
WP_020427049.1|7121939_7122377_-	50S ribosomal protein L13	NA	NA	NA	NA
WP_020427050.1|7122608_7123388_-|tRNA	tRNA pseudouridine(38-40) synthase TruA	NA	NA	NA	NA