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_CP049862	Sanguibacter sp. HDW7 chromosome, complete genome	10 crisprs	DEDDh,WYL,DinG,csa3,cas3	0	2	3	0

1. NZ_CP049862

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP049862_1

• CRISPR_ID: NZ_CP049862_1
• CRISPR_location: 14546-14629
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP049862_1

Consensus_repeat	Method
CCGGCACGGAGCCGTCGGGCAGCG	CRISPRCasFinder

spacers of NZ_CP049862_1

>1.1|14570|36|NZ_CP049862|CRISPRCasFinder
TCCCACCGGGCCGGGAGGCGGCACCCGACGACGCAC

CRISPR arrays and Neighbor proteins around NZ_CP049862_1

CRISPR arrays

The CRISPR arrays of NZ_CP049862_1

>merge|NZ_CP049862|1|14546-14629|CRISPRCasFinder
CCGGCACGGAGCCGTCGGGCAGCGTCCCACCGGGCCGGGAGGCGGCACCCGACGACGCACCGGGCACGGAGCCGTCGGGCAGCG

>NZ_CP049862|1|1|14546-14629|CRISPRCasFinder
CCGGCACGGAGCCGTCGGGCAGCG	TCCCACCGGGCCGGGAGGCGGCACCCGACGACGCAC
CGGGCACGGAGCCGTCGGGCAGCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP049862.1|WP_166412526.1|17573_17822_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412533.1|24398_25142_-|DUF2510-domain-containing-protein	unknown	unknown	gnl|CDD|378480
NZ_CP049862.1|WP_166412531.1|22480_23527_-|hypothetical-protein	unknown	unknown	gnl|CDD|237864
NZ_CP049862.1|WP_166412516.1|4192_5275_+|LPXTG-cell-wall-anchor-domain-containing-protein	unknown	unknown	gnl|CDD|223021
NZ_CP049862.1|WP_166412523.1|11274_12561_+|HlyC/CorC-family-transporter	unknown	unknown	gnl|CDD|224173
NZ_CP049862.1|WP_166412517.1|5289_5859_+|signal-peptidase-I	unknown	unknown	gnl|CDD|131283
NZ_CP049862.1|WP_166415115.1|6140_6632_+|low-molecular-weight-phosphotyrosine-protein-phosphatase	unknown	unknown	gnl|CDD|319971
NZ_CP049862.1|WP_166412525.1|15507_15945_-|heavy-metal-associated-domain-containing-protein	unknown	unknown	gnl|CDD|225328
NZ_CP049862.1|WP_166415117.1|16022_17522_-|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|183775
NZ_CP049862.1|WP_166412530.1|21486_22431_+|formate/nitrite-transporter-family-protein	unknown	unknown	gnl|CDD|225027
NZ_CP049862.1|WP_166412519.1|8042_9035_-|ABC-transporter-permease-subunit	unknown	unknown	unknown
NZ_CP049862.1|WP_166412522.1|10707_11124_+|(deoxy)nucleoside-triphosphate-pyrophosphohydrolase	unknown	unknown	gnl|CDD|239517
NZ_CP049862.1|WP_166412529.1|20541_21399_-|sugar-phosphate-isomerase/epimerase	unknown	unknown	gnl|CDD|224007
NZ_CP049862.1|WP_166412527.1|18121_18877_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224054
NZ_CP049862.1|WP_166412521.1|10452_10683_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225107
NZ_CP049862.1|WP_166412528.1|18858_20403_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412524.1|12875_14078_+|hypothetical-protein	unknown	unknown	gnl|CDD|227645
NZ_CP049862.1|WP_166412532.1|23683_24391_+|type-1-glutamine-amidotransferase-like-domain-containing-protein	unknown	unknown	gnl|CDD|153240
NZ_CP049862.1|WP_166412520.1|9034_10114_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213235
NZ_CP049862.1|WP_166412518.1|6761_7943_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl|CDD|235596

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP049862.1|WP_166412533.1|24398_25142_-|DUF2510-domain-containing-protein	gnl|CDD|378480	pfam10708, DUF2510, Protein of unknown function (DUF2510). This is family of proteins conserved in Actinobacteria. Many members are annotated as putative membrane proteins but this could not be confirmed.	0.00259593
NZ_CP049862.1|WP_166412531.1|22480_23527_-|hypothetical-protein	gnl|CDD|237864	PRK14950, PRK14950, DNA polymerase III subunits gamma and tau; Provisional.	6.11056e-05
NZ_CP049862.1|WP_166412516.1|4192_5275_+|LPXTG-cell-wall-anchor-domain-containing-protein	gnl|CDD|223021	PHA03247, PHA03247, large tegument protein UL36; Provisional.	0.0018523
NZ_CP049862.1|WP_166412523.1|11274_12561_+|HlyC/CorC-family-transporter	gnl|CDD|224173	COG1253, TlyC, Hemolysins and related proteins containing CBS domains [General function prediction only].	2.21261e-109
NZ_CP049862.1|WP_166412517.1|5289_5859_+|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.	1.51707e-24
NZ_CP049862.1|WP_166415115.1|6140_6632_+|low-molecular-weight-phosphotyrosine-protein-phosphatase	gnl|CDD|319971	cd16343, LMWPTP, Low molecular weight protein tyrosine phosphatase. Low molecular weight protein tyrosine phosphatases (LMW-PTP) are a family of small soluble single-domain enzymes that are characterized by a highly conserved active site motif (V/I)CXGNXCRS and share no sequence similarity with other types of protein tyrosine phosphatases (PTPs). LMW-PTPs play important roles in many biological processes and are widely distributed in prokaryotes and eukaryotes.	7.5526e-53
NZ_CP049862.1|WP_166412525.1|15507_15945_-|heavy-metal-associated-domain-containing-protein	gnl|CDD|225328	COG2608, CopZ, Copper chaperone [Inorganic ion transport and metabolism].	1.09432e-15
NZ_CP049862.1|WP_166412527.1|18121_18877_+|ABC-transporter-ATP-binding-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	6.23009e-79
NZ_CP049862.1|WP_166412520.1|9034_10114_-|ATP-binding-cassette-domain-containing-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.	5.43538e-86
NZ_CP049862.1|WP_166412522.1|10707_11124_+|(deoxy)nucleoside-triphosphate-pyrophosphohydrolase	gnl|CDD|239517	cd03425, MutT_pyrophosphohydrolase, The MutT pyrophosphohydrolase is a prototypical Nudix hydrolase that catalyzes the hydrolysis of nucleoside and deoxynucleoside triphosphates (NTPs and dNTPs) by substitution at a beta-phosphorus to yield a nucleotide monophosphate (NMP) and inorganic pyrophosphate (PPi). This enzyme requires two divalent cations for activity; one coordinates the phosphoryl groups of the NTP/dNTP substrate, and the other coordinates to the enzyme. It also contains the Nudix motif, a highly conserved 23-residue block (GX5EX7REUXEEXGU, where U = I, L or V), that functions as metal binding and catalytic site. MutT pyrophosphohydrolase is important in preventing errors in DNA replication by hydrolyzing mutagenic nucleotides such as 8-oxo-dGTP (a product of oxidative damage), which can mispair with template adenine during DNA replication, to guanine nucleotides.	1.02994e-34
NZ_CP049862.1|WP_166412530.1|21486_22431_+|formate/nitrite-transporter-family-protein	gnl|CDD|225027	COG2116, FocA, Formate/nitrite family of transporters [Inorganic ion transport and metabolism].	1.64347e-48
NZ_CP049862.1|WP_166412521.1|10452_10683_+|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].	6.52536e-16
NZ_CP049862.1|WP_166412529.1|20541_21399_-|sugar-phosphate-isomerase/epimerase	gnl|CDD|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	5.1298e-21
NZ_CP049862.1|WP_166412524.1|12875_14078_+|hypothetical-protein	gnl|CDD|227645	COG5340, COG5340, Predicted transcriptional regulator [Transcription].	0.000821592
NZ_CP049862.1|WP_166412532.1|23683_24391_+|type-1-glutamine-amidotransferase-like-domain-containing-protein	gnl|CDD|153240	cd03146, GAT1_Peptidase_E, Type 1 glutamine amidotransferase (GATase1)-like domain found in peptidase E. Type 1 glutamine amidotransferase (GATase1)-like domain found in peptidase E. This group contains proteins similar to the aspartyl dipeptidases Salmonella typhimurium peptidase E and Xenopus laevis peptidase E. In bacteria peptidase E is believed to play a role in degrading peptides generated by intracellular protein breakdown or imported into the cell as nutrient sources. Peptidase E uniquely hydrolyses only Asp-X dipeptides (where X is any amino acid), and one tripeptide Asp-Gly-Gly. Peptidase E is believed to be a serine peptidase having a Ser-His-Glu catalytic triad which differs from the Cys-His-Glu catalytic triad typical of GATase1 domains by having a Ser in place of the reactive Cys at the nucleophile elbow. Xenopus PepE is developmentally regulated in response to thyroid hormone and, it is thought to play a role in apoptosis during tail reabsorption.	2.0611e-44
NZ_CP049862.1|WP_166415117.1|16022_17522_-|SDR-family-NAD(P)-dependent-oxidoreductase	gnl|CDD|183775	PRK12826, PRK12826, SDR family oxidoreductase.	2.65402e-12
NZ_CP049862.1|WP_166412518.1|6761_7943_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl|CDD|235596	PRK05764, PRK05764, aspartate aminotransferase; Provisional.	1.03418e-127

Protein sequences

>NZ_CP049862.1|WP_166412524.1|12875_14078_+|hypothetical-protein
MTSSTPAPTAVGQLADGGTTDARTAGIRAADTGTPDARSSDARVPDARTTGVRADDHRARPRTLLATSTYVRPGSTTEVPVVPDDRVELARELPPGYVAGEVRAGNLVKLRRGAYVSTELAKADGYVGAHRRAVARVRAVAGVTLPDRTVSHVSAALLHGLPTWWLPARVHLSQPIEPRVRKGDDVVRHVVPVPDDDVVEIDGMRVTSLPRTVVDCLCTFRPWDALVLVDAALRRGVDVAELLERLAAKRGHRGVRRAATVLDAADAGAESPGVSLTRYVLLAGGLPRPSTQIEVATRHGTVWADLGWKDHRLLAEYDGEGKYATRADLMREKQREDDLREAGNQVVRVTKGDLRDPDGLVRRVAARLPMSARRARGDRAGLPQIPVARPASPPSPGGAR
>NZ_CP049862.1|WP_166412523.1|11274_12561_+|HlyC/CorC-family-transporter
MDQDTVLNVLLVIVFVLVGGVFAATELALVSLREGQLDKMEREGGRAARTARLARDPNRFLAAVQIGVTVAGFLSAAYGASTLAPDFAPLLVDLGLSTSAAATTSLIVLTLLIAYLSLVLGELVPKRLALQHTERLSRVVGPPLDRFARLMRPAVWTLSKSTNGVVRLLGGDPNARGDEMSDEELRGIVTGHEGLAPDEKRILGDVLDAGARSLAEVMRPRTEVAFMSADLTVSQALDVVADAPYSRYPVTGENFDDVLGFLHVRDLLRASDGVVVRDLVREILLLPSTNRLLPSMSQMRRDGVHIAVVVDEYGGTDGIVTLEDLVEELVGDIRDEYDADEPARERAADGIVRVDAGLTIEEFAEETGVVLEDGPYETAAGFVIDRLGRLAAEGDEILVGEALVRVAEVENRRIRTLEVTLPPAVPTV
>NZ_CP049862.1|WP_166412522.1|10707_11124_+|(deoxy)nucleoside-triphosphate-pyrophosphohydrolase
MERTQVVAAIIVDDLDAPSRVLGARRVRPERLAGRWEFPGGKVEPGESTDAALARELQEELAVTVRAGAELVGPHDDGWHVTDRHAMRLWFAVLTSPEPVPLAEHDELRWLDATSIDDVPWLDGDLEIVDALRPLLRR
>NZ_CP049862.1|WP_166412521.1|10452_10683_+|response-regulator-transcription-factor
MQPTEAHATGARLTPREIVVLTHLSDDVTLDDVARELFVSRNTVKTQVRSVYRKLGITTRAEAVAHARRLGLREDS
>NZ_CP049862.1|WP_166412520.1|9034_10114_-|ATP-binding-cassette-domain-containing-protein
MTTTFDGASPGDLAIMTRGLRKTYRSATGRRSVAVQGLDLDVPVGGVHGFLGPNGSGKTTSIRMLLGLIHADAGSMNVLGYEIPRQLPSVISRVGAIVEQPKFFPTISARRNLEILAKGIGAPDRAVAQVLEDVGLTERGKDLYKTYSLGMKQRLAIAATLLKDPDLLIFDEPTNGLDPAGIHEIRETMRSLGASGKTVLVSSHILSEVEHVADTVTIIGRGRTLAQGRVKDLLDAQSTTTVRVGVADPDGAERVLREGGLTVVREGATLNVTGADDPAEITRRLAHHELYVSELVAQRAGLEQFFLELTAGEGPGTSAGVPLPTHSSGQHAGPSAPPPPQAPSPNPYDRPTSTEGGEA
>NZ_CP049862.1|WP_166412519.1|8042_9035_-|ABC-transporter-permease-subunit
MRLIAAELLRARSRRATWIILSALVGLCLFFLGGNFVSTHMPTAQDRQYAQEAFEESTKYWEENGQADYDSCVSDATLGNSTPEDWGCSGILEKPVLENFLWSPPGFAERVTSDTSGLLILAAAIMVLLGASLTAAEFASGSLGNWLTFAPRRTPVFFSKLAAPAVIALGAALLVAALSVLGTFAWTELRGIPSPEPLETDKLVWMILRSTGVVVVAGVLGAALGALLRHTAAVIGVVGGYFVVVEMVFAGIFWESGLQRWFLSTQLQAVTQGKASYYVQVCTWNEEQQYRTCESLEKFVTAADATLFLGSIGLVLVVVSWLVFRRRDVH
>NZ_CP049862.1|WP_166412518.1|6761_7943_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MKVSQRAAVSPFAVMQIIAAANARRAAGQDVINLCAGEPVTGASDAVRERAREFLDGRSLGYTEALGAPALREALAGHYARWYGLDVDPARIAVTTGSSGGFMLAFLAAFDVGDRVALVRPGYPAYRNILASLGCEVVELAAGADVGYAPTPAMLDVAHAEAPLAGLVVASPANPTGTMIDAARLTELAAWCAEHDVRLVSDEIYHGIVHDRARWPGATAAHHLGTGAVVVSSFSKYWAMTGWRLGWLVLPEDLLEPVDALAGNVALCPPALAQHAAVAALEPAGYAAAARDAEQYGRSREVLLARLGELGWHDVAPADGAFYLYADISASGLDSREWCARLLDEAGVALTPGTDFDPVDGHRWVRLSFAQEPTTITAAVDRIVAWQRTLTSS
>NZ_CP049862.1|WP_166415115.1|6140_6632_+|low-molecular-weight-phosphotyrosine-protein-phosphatase
MTVCTGNICRSPMAEIVLRHHLEEAGLGGHVTVDSTGISDEEHGRPVDRRARTALEARGYVVGDHRARRVRADELPARDLVLAMTQHHARVLRSMLPLGDERVVMFRAFDPTAPAVVDGDERVLDVDDPWYGGSEDFETCLDQVEAAAAGVVAHVRALLAARA
>NZ_CP049862.1|WP_166412517.1|5289_5859_+|signal-peptidase-I
MVSRTASVVSRIVLLAGLALVVLVVVVPATTGAVALAVLTGSMAPTYPAGSLVVVRPVDVDELRAGDVVTYQAESGRATLVTHRVTGVEHRSDGTLRLVTQGDANRVPDPEPVRAEQVVGQVWYAVPHVGRLTTALDGHTRGAALALVAGALLAHGAWHVVTGLRERRRRPVAAPAAASGSEHRPGRAA
>NZ_CP049862.1|WP_166412516.1|4192_5275_+|LPXTG-cell-wall-anchor-domain-containing-protein
MRHRAIIAVLLAAVLGGASSGAAWARWQARVPVHGGIQVTRVVTLPAPVEPSTPVVPSAPAETSALSESVEPASPVEPAETAGPVEPAAAVGPARAEGAGTVVPAVYSAAVHSAASTARARAVRTAAADGTVEGSAGILVSADGRTFAPDLTTGIFPDTTRMVPGGTTSADLWVRSSGDVDARLRLELLDVAADDPDLAAALTLGVDAVADGTATTTPTTVAEADACTVLVRDIDLPAGRTVHLRATAALGNLVGTQGQGSSATFRYRVVASDTRLTAPEDPGACAEGEPDGASTAPPTTPQPDDGADGPGTLPATGAQVVLLAAGASAMLLLGGMLRRRRGGQRSVAAASSAPTDARRP
>NZ_CP049862.1|WP_166412525.1|15507_15945_-|heavy-metal-associated-domain-containing-protein
MPTITTLDVTGMTCGHCVSAVTKELEAVSGVKNVSVDLNVGEASEVTVVSDDPLAEDALRAAIDEAGYEVTGISTHGSAEEFSQLADTRSEVYAGTSHIGSGSATAVGPVGIALTPREDVDAAVLEQSDAPAAGGCGCGGCGCGN
>NZ_CP049862.1|WP_166415117.1|16022_17522_-|SDR-family-NAD(P)-dependent-oxidoreductase
MLEHVSDTPQLNPDELARALEILEAANALPPEHPDKVALQRATAKLYKTVKKQRRDDAKAAVQDADRAVIEATATGASTRIDDETEGVDIRPGSATGTFAGRLSKPQGCYVCKEPYQDVDVFYHQLCPRCAAENRAKRDARTDLTGRRALLTGGRAKIGMYIALRLLRDGAQLTITTRFPNDAVRRYAQMEDSADWIHNLTVVGIDLRDPAQVMALADDIASQGHLDILINNAAQTVRRSPGAYAPLAAAESAPLPELPYLPPVTTYGRSVDAHPAALEASVRAGGRDHGTPVSTHVEESVTAPGLLTKLALTAGSASLDRVATGTAIDAGGLVPDLVSQNSWVDRVDQVDPLEMLEVQLCNETAPFILVSRLRAALAASPARRTYVVNVSAMEGQFNRGYKGPGHPHTNMAKAAVNMLTRTSSREMFESDQILMTSVDTGWITDERPHTTKARLHEEGFHAPLDLVDGAARVYDPIVRGEDGEDVFGVFLKDYKPYAW
>NZ_CP049862.1|WP_166412526.1|17573_17822_-|hypothetical-protein
MSELLGTTAASTIVLRSLAGVAVALFFVVVTSLFWDLPAPIDRAATPLLAGVFMLTVIVREWSRRTHGQSDSGDGAHAASSG
>NZ_CP049862.1|WP_166412527.1|18121_18877_+|ABC-transporter-ATP-binding-protein
MDVALGLEGLRKTFGEKVAVERVDLAVPAGSFYGLVGPNGAGKTTTLSMATGLLRPDAGRVTVRGTDLWADPVAAKSLLGVLPDGVRLFDRLTGLQLVVHAGMLHRLPRATARERAEALLRALDLEADANTFVADYSAGMTKKIALACALVHAPRLLVLDEPFEAVDPVSAASIRAILADYVATGGTVVVSSHVMDLVERMCDHVAVLAAGRVLAAGTVDEVRGGASLEDRFVELVGGRRSGEGLEWLHSS
>NZ_CP049862.1|WP_166412528.1|18858_20403_+|hypothetical-protein
MVAQLLSLRWQVYLGTLRRSVWQTIGAVVALVYAVGLGGMVAVAGLVGGLRSDLTGPVVVGGALLVLVWSVGPLVAFGLDDTFDPRRLAPFPLSTRDLLLGTAISTLLGPGGIFTIIAALGLIAAWVTQPLALLVALVGVPLGVVTAVLGGRAVTTAARPLVEGRRGRDIAAAMAVLAVSLVGPAVLLLGSFEITPESIDHLAPWFAWTPFGAAFALPGDVAAGAWVLLAGHLAIAVATPALLLAWWRRSLATQLTRPPQASAGHGKGLGVLARVPDTPAGAVVARCLTYWVRDPRYSTSLISVPVIVVLGSVFAGDGVWLLAAAPVVAWTLGWAISVDVAMDSTAFWTHVAAPLRWADDRWGRVLAIGVPGAVLTIATVLWTLLRTDRWDAALAMLGVSIATLLASLGLASIVSALVVFPVNQPGDNPFGSKQGGSMGAMLSQMVGTFVLAVLLAPAGVLTVLAVARGSAAFGAAAAVVGLVTGVVVLLVGVRVGARRLTASAPELLARLKSF
>NZ_CP049862.1|WP_166412529.1|20541_21399_-|sugar-phosphate-isomerase/epimerase
MAGETSARPHVTLSTASVYPRKAPLAFELAADLGYDGVEVMVWNDKISRDDVALAHVARETGVQIRSVHAPTLIVSQQVWGTKPGHKLAKTVDMALTLGASTVVVHPPFAWQRGYSRHFAEQVRSLSEDSGLTIAVENMYPWRGRKREFMGYLPGWDPTEHDYDRVTLDVSHAATSRQSCVDLAALFGPRLAHVHLTDGTESGFDEHLVPGRGTQPVRELLQGLAHSDFSGDVVVEIGTRKARDATERRADIAQSLHFARTYLAVDAHAEFSPAPEHHRPQSPWA
>NZ_CP049862.1|WP_166412530.1|21486_22431_+|formate/nitrite-transporter-family-protein
MAASPEKLFPGKTFVSTVLDAAEAKVEMSRSITQVYLMRAAMAGILIGIFYLANYTIIAGFVAIDPDLRTVGRLVGAFVFGFALVFIYFTRSELLTSNMMIVTIAMYHHRMRARHASGLLALCLLGNALGGLLIALLVAGSSMIDDTTGELVASSVEHKLDYVTSGASGMLDLFVRAILCNLLINLAMLLVYNGLVKADGVKVLAMNVAVMLFAFLGYEHSVANTVLFVVQGFHGGVAVWPAVANVAIAVVGNFVGGGLLIGWYYAYANDPQRTQRALLREARLVTRGTARSGAATDDARAERVTVDGDELPGA
>NZ_CP049862.1|WP_166412531.1|22480_23527_-|hypothetical-protein
MSPRPAAPRTPSESTPAAPTSRPQPTLPTRPSLVTIAASVLTAVTSTVALSYLGVGGTIIGAVVAAILTAFANYAYTRSLVHTQVVVTQLAPRYLRTTTSAEDTAVIDAVPTDAPHADATATGLLEPTVTTDVIPVAAAPEVAIATREMPVVARVLEESTGPSANSSAPAPLDERVGRDLMAPARRSPRRTFALVTVTTFVVIILTLTAVEIGLGRPLSKALRGIEGSGTTISRVREKSRPVTPTQNPTTSPSEEPTDASTTPTEEPTTPEPTETPTPTPSDEPTDPATTVPPTTPTDVPTDAPTPELPRPGGTPVPEPPAPQDDATAPADASTEGASAADDATTPAA
>NZ_CP049862.1|WP_166412532.1|23683_24391_+|type-1-glutamine-amidotransferase-like-domain-containing-protein
MTTHVLALGGGGFSMSDGYSATALDRYALGLAGVERPTVCFVPTASGDATVYIERFEAAYAPLDCETRVLRLVADGAQSVARTLDGVDVLMVGGGSTVNLVALWDVHGVTRELRRLAGGRDLVLAGLSAGANCWFEGCTTDSFGPEVVPWRGGTGFVAGSFCPHADGEDRVGDYAAAVASGALPAGWAADDGAAVHVVDGVVRAHLAERPGARTYRLEADGAGRASVVAQSMTLL
>NZ_CP049862.1|WP_166412533.1|24398_25142_-|DUF2510-domain-containing-protein
MTAQPPPLPGSTPDGTVQSGTGSAPRGTVSAPGGGGDVLVGPAGWYPHPDGGERWWDGIAWTNLSRKGDKISHVGGGGSSYADDARDRRRGAFKFFAALVVLFLLWSLGIAGWEVLGQRYPQFERVTPAERATAVLSAPRGLGTGDACPTTDRQLVDPASADVARWRELRGCDLTPALDREVWEWVTKPTEDSPTAVVDYTFAKVEDAERPDAKLGGTTVRLTLTLEKALLGWKVSAVEGLPARAKG

Crispr_ID: NZ_CP049862_2

• CRISPR_ID: NZ_CP049862_2
• CRISPR_location: 61773-61861
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: DEDDh

Consensus repeat of NZ_CP049862_2

Consensus_repeat	Method
CGACGTCCACCGATGACGGTGGCGTCGGTGAC	CRISPRCasFinder

spacers of NZ_CP049862_2

>2.1|61805|25|NZ_CP049862|CRISPRCasFinder
GAGGAGGGCGACGGCGACGACTCGT

CRISPR arrays and Neighbor proteins around NZ_CP049862_2

CRISPR arrays

The CRISPR arrays of NZ_CP049862_2

>merge|NZ_CP049862|2|61773-61861|CRISPRCasFinder
CGACGTCCACCGATGACGGTGGCGTCGGTGACGAGGAGGGCGACGGCGACGACTCGTCGACGTCCACCGGTGACGGTGGCGTCGGTGAC

>NZ_CP049862|2|2|61773-61861|CRISPRCasFinder
CGACGTCCACCGATGACGGTGGCGTCGGTGAC	GAGGAGGGCGACGGCGACGACTCGT
CGACGTCCACCGGTGACGGTGGCGTCGGTGAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP049862.1|WP_166412569.1|69809_70385_+|ATP-binding-protein	unknown	unknown	gnl|CDD|379324
NZ_CP049862.1|WP_166412561.1|58890_59586_+|DUF218-domain-containing-protein	unknown	unknown	gnl|CDD|225500
NZ_CP049862.1|WP_166412553.1|48190_50320_-|S9-family-peptidase	unknown	unknown	gnl|CDD|224423
NZ_CP049862.1|WP_166412564.1|62136_62616_+|hypothetical-protein	unknown	unknown	gnl|CDD|367797
NZ_CP049862.1|WP_166412558.1|53048_53489_-|hypothetical-protein	unknown	unknown	gnl|CDD|225598
NZ_CP049862.1|WP_166415119.1|72482_74171_-|amidohydrolase	unknown	unknown	gnl|CDD|238625
NZ_CP049862.1|WP_166412565.1|62892_64533_+|ABC-F-family-ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|223562
NZ_CP049862.1|WP_166412566.1|64529_65351_-|NYN-domain-containing-protein	unknown	unknown	gnl|CDD|350237
NZ_CP049862.1|WP_166412555.1|51286_51634_+|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224639
NZ_CP049862.1|WP_166412571.1|71096_71717_-|3'-5'-exonuclease	DEDDh	cd06127_DEDDh_CAS-I	gnl|CDD|176648
NZ_CP049862.1|WP_166412560.1|58273_58747_-|hypothetical-protein	unknown	unknown	gnl|CDD|235136
NZ_CP049862.1|WP_166412572.1|71781_72339_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412554.1|50430_51237_+|MerR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|133378
NZ_CP049862.1|WP_166412556.1|51630_52602_+|DUF1648-domain-containing-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412559.1|53566_58225_-|ATP-dependent-RNA-helicase-HrpA	unknown	unknown	gnl|CDD|182986
NZ_CP049862.1|WP_166412567.1|65519_66719_+|exonuclease-subunit-SbcD	unknown	unknown	gnl|CDD|182871
NZ_CP049862.1|WP_166412562.1|59595_60204_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412557.1|52620_53052_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412568.1|66718_69808_+|SMC-family-ATPase	unknown	unknown	gnl|CDD|223496
NZ_CP049862.1|WP_166412570.1|70523_71000_+|M15-family-metallopeptidase	unknown	unknown	gnl|CDD|350624

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP049862.1|WP_166412571.1|71096_71717_-|3'-5'-exonuclease	DEDDh	cd06127_DEDDh_CAS-I	6.5e-39	128.4	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP049862.1|WP_166412569.1|69809_70385_+|ATP-binding-protein	gnl|CDD|379324	pfam13671, AAA_33, AAA domain. This family of domains contain only a P-loop motif, that is characteristic of the AAA superfamily. Many of the proteins in this family are just short fragments so there is no Walker B motif.	3.33467e-05
NZ_CP049862.1|WP_166412566.1|64529_65351_-|NYN-domain-containing-protein	gnl|CDD|350237	cd11297, PIN_LabA-like_N_1, uncharacterized subfamily of N-terminal LabA-like PIN domains. This N-terminal LabA-like PIN domain is found in a well conserved group of mainly bacterial proteins with no defined function, which contain a C-terminal LabA_like_C domain. LabA from Synechococcus elongatus PCC 7942, (which does not contain this C-terminal domain), has been shown to play a role in cyanobacterial circadian timing. The LabA-like C-terminal domains characteristic of this subfamily may be related to the LOTUS domain family (which also co-occurs with LabA-like N-terminal domains). The function of the N-terminal domain is unknown. The LabA-like PIN domain family also includes the N-terminal domain of limkain b1, a human autoantigen localized to a subset of ABCD3 and PXF marked peroxisomes. Other members are the LabA-like PIN domains of human ZNF451, uncharacterized Bacillus subtilis YqxD and Escherichia coli YaiI. Curiously, a gene labeled NicB from Pseudomonas putida S16, which is described as a putative NADH-dependent hydroxylase involved in the microbial degradation of nicotine also falls into the LabA-like PIN family. The PIN (PilT N terminus) domain belongs to a large nuclease superfamily. The structural properties of the PIN domain indicate its active center, consisting of three highly conserved catalytic residues which coordinate metal ions; in some members, additional metal coordinating residues can be found while some others lack several of these key catalytic residues. The PIN active site is geometrically similar in the active center of structure-specific 5' nucleases, PIN-domain ribonucleases of eukaryotic rRNA editing proteins, and bacterial toxins of toxin-antitoxin (TA) operons.	2.34087e-67
NZ_CP049862.1|WP_166412553.1|48190_50320_-|S9-family-peptidase	gnl|CDD|224423	COG1506, DAP2, Dipeptidyl aminopeptidases/acylaminoacyl-peptidases [Amino acid transport and metabolism].	9.77238e-62
NZ_CP049862.1|WP_166412564.1|62136_62616_+|hypothetical-protein	gnl|CDD|367797	pfam04073, tRNA_edit, Aminoacyl-tRNA editing domain. This domain is found either on its own or in association with the tRNA synthetase class II core domain (pfam00587). It is involved in the tRNA editing of mis-charged tRNAs including Cys-tRNA(Pro), Cys-tRNA(Cys), Ala-tRNA(Pro). The structure of this domain shows a novel fold.	2.91452e-29
NZ_CP049862.1|WP_166412565.1|62892_64533_+|ABC-F-family-ATP-binding-cassette-domain-containing-protein	gnl|CDD|223562	COG0488, Uup, ATPase components of ABC transporters with duplicated ATPase domains [General function prediction only].	4.66342e-105
NZ_CP049862.1|WP_166412561.1|58890_59586_+|DUF218-domain-containing-protein	gnl|CDD|225500	COG2949, SanA, Uncharacterized membrane protein [Function unknown].	1.18766e-47
NZ_CP049862.1|WP_166412555.1|51286_51634_+|GntR-family-transcriptional-regulator	gnl|CDD|224639	COG1725, COG1725, Predicted transcriptional regulators [Transcription].	1.0572e-23
NZ_CP049862.1|WP_166412571.1|71096_71717_-|3'-5'-exonuclease	gnl|CDD|176648	cd06127, DEDDh, DEDDh 3'-5' exonuclease domain family. DEDDh exonucleases, part of the DnaQ-like (or DEDD) exonuclease superfamily, catalyze the excision of nucleoside monophosphates at the DNA or RNA termini in the 3'-5' direction. These proteins contain four invariant acidic residues in three conserved sequence motifs termed ExoI, ExoII and ExoIII. DEDDh exonucleases are classified as such because of the presence of specific Hx(4)D conserved pattern at the ExoIII motif. The four conserved acidic residues are clustered around the active site and serve as ligands for the two metal ions required for catalysis. Most DEDDh exonucleases are the proofreading subunits (epsilon) or domains of bacterial DNA polymerase III, the main replicating enzyme in bacteria, which functions as the chromosomal replicase. Other members include other DNA and RNA exonucleases such as RNase T, Oligoribonuclease, and RNA exonuclease (REX), among others.	9.92374e-48
NZ_CP049862.1|WP_166412560.1|58273_58747_-|hypothetical-protein	gnl|CDD|235136	PRK03598, PRK03598, putative efflux pump membrane fusion protein; Provisional.	0.00010956
NZ_CP049862.1|WP_166412554.1|50430_51237_+|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.	9.51823e-14
NZ_CP049862.1|WP_166412568.1|66718_69808_+|SMC-family-ATPase	gnl|CDD|223496	COG0419, SbcC, ATPase involved in DNA repair [DNA replication, recombination, and repair].	8.2615e-59
NZ_CP049862.1|WP_166412559.1|53566_58225_-|ATP-dependent-RNA-helicase-HrpA	gnl|CDD|182986	PRK11131, PRK11131, ATP-dependent RNA helicase HrpA; Provisional.	0
NZ_CP049862.1|WP_166412567.1|65519_66719_+|exonuclease-subunit-SbcD	gnl|CDD|182871	PRK10966, PRK10966, exonuclease subunit SbcD; Provisional.	2.0673e-54
NZ_CP049862.1|WP_166415119.1|72482_74171_-|amidohydrolase	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.	1.03741e-129
NZ_CP049862.1|WP_166412558.1|53048_53489_-|hypothetical-protein	gnl|CDD|225598	COG3056, COG3056, Uncharacterized lipoprotein [Cell envelope biogenesis, outer membrane].	0.00478284
NZ_CP049862.1|WP_166412570.1|70523_71000_+|M15-family-metallopeptidase	gnl|CDD|350624	cd14852, LD-carboxypeptidase, L,D-carboxypeptidase DacB and LdcB, and related proteins. This L,D-carboxypeptidase family includes LdcB LD-Carboxypeptidase from Streptococcus pneumoniae, Bacillus anthracis, and Bacillus subtilis, and L,D-carboxypeptidase DacB from Streptococcus pneumonia and Lactococcus lactis. These enzymes are active against cell-wall-derived tetrapeptides and synthetic tetrapeptides lacking the sugar moiety but are inactive against tetrapeptides terminating in L-alanine. L,D-carboxypeptidase DacB plays a key role in the remodeling of S. pneumoniae peptidoglycan during cell division. It adopts a zinc-dependent carboxypeptidase fold and acts as an L,D-carboxypeptidase towards the tetrapeptide L-Ala-D-iGln-L-Lys-D-Ala of the peptidoglycan stem. This family also includes vanY D-Ala-D-Ala carboxypeptidase which is vancomycin-inducible and penicillin-resistant. VanY hydrolyzes depsipeptide- and D-alanyl-D-alanine-containing peptidoglycan precursors; it is insensitive to beta-lactams. All these enzymes belong to the MEROPS family M15 subfamily B.	9.99259e-23

Protein sequences

>NZ_CP049862.1|WP_166412562.1|59595_60204_+|hypothetical-protein
MSVDRPATYARTGQRCTPPAPGDATVGLLLLVLPLLALVVWVKDEESELTRGWLLAFVIVYALGAVVALRGFTSDASPLRMERRFVPMRYLVLAVVWAVGLPWGVAMLLAPGTAAAQEAATRGEILGTPTPTATASDGSLLPVEPPSDLDLWVASGGTVMYGQLVVLASVACFAVLVVLYVRARRAQLERFPTPGQFDVVER
>NZ_CP049862.1|WP_166412561.1|58890_59586_+|DUF218-domain-containing-protein
MTTPVDLAPVAVRPRRRVPRTLVVAVCAWVVAVALPVVVVQVSGRQHVVDLADAPPRTVALVLGAGLRPDGSPSTYLARRLDAAVNLYERRVVRGVLVSGDSSTVGYDEPTAMKDYLVRQGVPADVVRQDFAGLDTHDSAVRARAVFGVRDAIVVTQDYHLPRAVFSARAAGIDAVGVAVSSESVTPEQLATWKARDLLASWKAAVDALVGRKPARPWSDEPGVADVLAGR
>NZ_CP049862.1|WP_166412560.1|58273_58747_-|hypothetical-protein
MSARRLTALAVAALLGASALAGCSEDGSFTLPSGDQLKQMVDDGSKQANELKAKAAEARASLEGLTGDLRGTAEKAVGQAQGAADQAKAALDAARDAKGDAEAQVDAARTALDKARADVEAARDRLAKDDSAAGKAANDALTKVEADLDKLLGELKN
>NZ_CP049862.1|WP_166412559.1|53566_58225_-|ATP-dependent-RNA-helicase-HrpA
MPVSTPSGSTAPEGRPRRGRGGRGRGPAQGAPQGSTQGSPQRGGRNGGRGGRDTFDRATLDARALARAARSAEIRGRVDVPAITYPENLPVSGQRGEIADAIRDHQVVIVAGATGSGKTTQLPKILLDLGRGRAGQIGHTQPRRLAARTVSERIAEEIGDEHTGPDGQVRRGRTGGVVGYQVRFTDESSDRTLVKVMTDGILLAQIQRDPLLRAYDTLVIDEAHERSLNIDFLLGYLTQLLPQRPDLKLVITSATIDSERFAEHFASVAPDGTRVPAPVIEVSGRTFPVEIRYRPLVEDAPDPADERGTSSGAVGGGKAGKKKRPARSVERDLMTGICEAVDELFAEGPGDILVFLSGEREIRDAADALRGHLGDRVDGRGTPLSVEVVPLYARLTAAEQHRVFEPHGGRRVVLATNVAETSLTVPGIRYVIDPGTARISRYSKATKVQRLPIEPVSQASANQRSGRCGRVADGIAIRLYSESDFEGRPEFTDPEILRTSLASVILQMISSGVATGPDDVASFPFVDPPDVRAVRDGVNLLTELGALGESASLTATGRTLSRLPMDPRLGRMIIEGARRGVGREVLIVTAVLSIQDPRERPTEQRQHADQLHGRFADPTSDFLTYLNLWEYLKEQRRALSSSAFRRLCKSEFINFLRVREWQDLVGQLKDMAEQLELEIKPASRAVVADGSGSGVVRRSAPGARALSVAEAMAEAAEKAGEAPEAETHRFRWDGDTIHRALLAGMLSQIGMQQVTEVGAQRPGRPTREDRRAAKQARNEYVGARNAHFAIFPGSPLSKKPPAWIMAGELVETSRLWAREVARIEPEWAEEIGAHLVKRVYSEPHWSSKQGAAQAFEKVLLHGLPVVAQRKVLFSRVDPEGAREMFLRKALVEGEWSTRHEFFARNRELLEEAEQLEARTRRRDLVVDDDTLFAFYDARVPADVVSARHFDRWWKDARRTDPELLTFTPELLVPEAADVDLADYPDMWEQGDLRLPLTYELSPGQQSDGVTVHVPLAVLDRVVPDGFGWLVPGMWTELATATIRALPKPVRVQLVPAPDVARDVVAWLRANEASWADLTRAGDMAPSFQEAFARAVRALRDVVVPDDAWAGVDLPGHLRMQFRVVDSRGTIVDEGADLLALQRRLRARTQAEVRTAVRTALADALREAGTTTPSSPTDPTRSAPAHSDAPSDATRRSGAPSESAGDLRVGPSDPTRSAPAHSDATEPAGVLLAEQDRLTTWPTLTSPTGEPVPGDVLPDEVVTRLGAGPSATTVRGYPAFVVELAPAGAKGGRNVESVALRILADRRRQAPDHAAGVRALLLAETGLQTPHVTTRWTGQQALTLASSPYRNTEALVADVQKAAIAALTSGDEPGIPEASTIRSREAYEAARGAVRERLEERVHQTVGHVVAALAAARELDTQVRGATSLALLNTLTDVRDDAARLIFDGFVTATPPERLRHLPRYLRAASHRLTKAEQNPNRDAELAWKIRDVEDLYDRARAAYAAGKPDAARLAALDEARWMLEELRVSFFAQQLGTDGTVSEKRIRGLLAG
>NZ_CP049862.1|WP_166412558.1|53048_53489_-|hypothetical-protein
MRTHRIAVVAAAALALAGCAASEASIDYVPPSISAAPTAAPGATITVTGAEFIADRRDKVRYDVFGREHPKDRSHPAEDIEVVLVVGEVRTTLTTVDASADGTWAATVVVPTTTPPGKATLEADADGLAVPASTSLTLEATSGEAS
>NZ_CP049862.1|WP_166412557.1|52620_53052_-|hypothetical-protein
MNRRGGAALAAVALLLGACAGPTAADEPRSAASCVGPQIRLDGAMTADVAPGDDVTVTGELFYSTCDDVGPGFDERTPYGALTLTAVVDGARFDVGTVTPDAEGSWSVAWHVPEGAVGSAAIEADDGRWAISLDTSGAHLVGD
>NZ_CP049862.1|WP_166412556.1|51630_52602_+|DUF1648-domain-containing-protein
MTTTTRDVPHRKVTALLTLVVPLLVLTAAILLVLSWRDELPAQVATHWGDDGVDQVGSLASMLVPFTIITVLFSLAMWALGTFAGQAAMTRRFVAGIAVWLAFFLGGMLVVTFDAQRGLTDAHDATGIGGGVAVSVLVACVAGIAAAVVVPRDPHRPARAAIPATTTTLPLDVDTRAAWVQQVRQGHAWLIVAGIVVAALGLGIATEWWIGLILAVGLVPLLTLLNGTVTVDKRGLTARTVFPWPRITVPLDEVENVGVVQVAPLSEFGGWGIRTALDGSIGMILRKGEAIEVRATGGRRIVVTVDDAATGAALLATLAGRGR
>NZ_CP049862.1|WP_166412555.1|51286_51634_+|GntR-family-transcriptional-regulator
MLLTLDPAAPEPLFEQLAAQLRAAIAAGELSAGDRLAPARDVAASLDINLHTVLRAYQELRDEGLVELRRGRGATVAARLDDDALRAAITTLVAESRRLGLDPRTTTALVKEALR
>NZ_CP049862.1|WP_166412554.1|50430_51237_+|MerR-family-transcriptional-regulator
MTTTWTTGTLARTLGVSEKAVRLWTERGLLTATRDDDGPRAYAVDQVVRGRAVVLLRALDVALADVAEVLDADDPVAAFDRLWGAARAALEGRLAAAGYVRSVLAGRPALDVPHEVRDVPGRLLLTLEATATLGELASCLPATTDRLFEALVEAGGTLAGPPSVVYHERATEYSAARITVRVPVMEPIAPPPGMALVAEEGGREVVVALDQDRSADQSFIIAVHDHVAYAAGDGTLAVVGDNRESYLPTWGRGLGGPVLEISAPVAPR
>NZ_CP049862.1|WP_166412553.1|48190_50320_-|S9-family-peptidase
MTPDAPATPFSDLDDFVALPRLGGLALSPDGLRLVTGVATRHPDGDRYVTSLWEVDPLGQVPARRLTRGAKGESQAAFASDGALLFVATRPGGDDDEKARLWELSAGGGEARTLASHPGGIGSVTVARGSGTVLVGASAFVRSGDVADDAERRKVRDDAKVAAILHDGYPIRYWDHDLGPSMPRIYALDGTPTAAPVAQASGTDASGTDAHVPHPATLLDDATPAVLRDLTPDAGAALDDSAWDLAPDGTWLVAEWRVPEGRATLGTGLVRIDVTTGERTDLLTADATHDHHAPRVSPDGTHLVWVRSERSTPSAGPRNELWLLDLATGDRRRLGADWDGWPGQVAWLPDGSGLVMTSDWQGRGPVFRVDVASGDVVRLTDEGVFTDVVVAPDGSAVFALRSSWEHPAEVVRVALDVTEGGFAQVTALQGPAQRPALPGTLTEVTTTAADGTPLRAWLALPDGASADAPAPLVLWIHGGPLGSWNGWSWRWSPWLLVAQGWAVLLPDPALSTGYGQAMIERGWGRWGAEPYTDLLAITDAAEARPDVDETRTAAMGGSFGGYMANWVAGHTDRFRAIVTHASLWSLETFLPTTDHASYWAREMTPEMRAAWSPHRSVGEIRTPMLVVHGDKDYRVPIGEGLSLWYSLLSASGLPQEADGSTVHRFLYFPDENHWVLKPQHAKVWYATVRGFLAQHVLGADPLDPVATLG
>NZ_CP049862.1|WP_166412564.1|62136_62616_+|hypothetical-protein
MTTVPADGAARARAALEASGIPFTVTTHGRVSSLAEAAAVRGVEPSGIIKTLVVRRGEGDFLFVLVPGDRQISWPKLRELLGVARMSMPDAAVALEVTGYERGTITPFGSTTAWPVVADERVVGQVSIGGGAHGTAATVDGADLVRVLDATVADVTDPA
>NZ_CP049862.1|WP_166412565.1|62892_64533_+|ABC-F-family-ATP-binding-cassette-domain-containing-protein
MTHPSHVALRARDLTRTYGDRHVVHDVSLDVVAGQRLALVGENGSGKSTLLRLLAGLEAPDAGTLEAPDDRALLAQDADPVDARTVGQLLDDAVSHVRAVERELEDAAAGLGGTSEHDDRPADVVDPGARYDAALAAAEAAGVWDVDARLGRTLAGLGIADLDRARPLRALSGGQRRRLDLAALLVCRPALLLLDEPTNHLDDAAADHLTSELLAYPGAVVVASHDRTLLDAVSTAVLDLDDDGPPVGGTFSDHLARRRAALAAWAARYAAEQDEIARLHDALDEGDGVARRVAPGRAMKDANKMAYGRWGDRVEQQVARRVKDARRRLDELVVAGTPRPPEPLRFRAPSGAGAVSGGGAVPGGGVRLVGAGVDGRLAPLSIDLPPGGRLLVTGGNASGKSTLLHLLAGDLAPTTGTVEVGAGGVALLEQEVGLAADARTPREVLAALARVRGDDPDDVDPHGLLAARDLDRPLAELSVGQRRRAVLAMVVRQSAGLLLLDEPTNHLSLRLAGELRDALEGWPGTVVVATHDRWWRAGWTGEVLGI
>NZ_CP049862.1|WP_166412566.1|64529_65351_-|NYN-domain-containing-protein
MAAPNGSQRRLAVLVDADNASAAIIEGLLEEVARYGVATVKRIYGDWTSQQMNSWKRVLLAQSLQPVQQFAYTAGKNATDSALIIDAMDLLHTGDLDGFCIVSSDSDFTRLASRLRESGKKVYGFGEEKTPEAFVAACDQFIYTDVLRRPAADPAPVPTGPSKGASPVTTPKKPQPVPFRFICQAIDDISGDDDWALLSQLGSHLTKLRPGFDPRLYGFTKLSTLLAAQPDLEVTQAVVGNGATAVVRIRPSASPALSAAAKSTAPTRATATP
>NZ_CP049862.1|WP_166412567.1|65519_66719_+|exonuclease-subunit-SbcD
MRILHTSDWHLGRTLHGVDLLGHQADFLDHLVAVVREREVDAVIVAGDVYDRAIPPVEAVRMLSDVLRRLSEVTQVVLTPGNHDSATRLGFGAELMRDGLHVRASVADVATPVVLRNRDGGVGAYVYALPYLDPDDARHRLVDPGEEPLARSHEAVTAAATERVLADLAERRASDAVRVPSVLVAHTFVVGGEASESERDIRVGGVDNVPSGVLRGVDYVALGHLHGPQRVPVADGPDGARTVARYSGSPLAYSFSEKDHHKSTVLVELGPDGVVDEPELLPAPVPRRLADVRGTFEEVTGALGAAHAEDWVRVTVTDAQRPEHLVLRIKDVMPHALVVLHEPPDRGGSTGPRAVTSVSDPFDVCCGFVEHVRGGAPDDTEQAVLRDALEAAQRTEVSA
>NZ_CP049862.1|WP_166412568.1|66718_69808_+|SMC-family-ATPase
MRLHTLTFQAVGPYPDRHTIDFARLGASGLYLLEGPTGAGKSTIIDAIVYALYGKVAADAASEDRLRSTRVGPGTESYVDLVLETGQGIYRVRRSPAYDRPKQRGTGTTKQQATAKLWRLSTADLDAIDPGRDLGDQTPGTFISGRADEVGTEVTRIVGLSREQLVQTIVLPQGEFASFLRAKPEDRSALLQRVFGTEIYQRVQNRLVEARKAALAARKEADAHIALAAAGLASGLDDDDAAELRALAAATDGSGPLLTRVDEHLVRIEAENVAAVAARDAASAEHATREGVARAARSSLSLVTRRDSAVGRLAELDARAEEHAHDTARLGAARRAATVVARLDDVEAADTRRTATAAALVDVRAAAAEHPVVATLLAAPDADAAVLAAARGTSATKLEHLVELETGLAARAETLDQRTAALVSQRTADEADVVELGGRPEARGALAARLATAQQGAALVPQRETEHAAAAAAQTAVAALARHDLRATEADTILANRVAAARTAVEDESRLRLARIDGIAGELARDLVPGEPCVVCGSTTHPAPAPLGDDHVSPEQVDAAAEARAAAEAEAQKARDARAALDAERATLVERTGGLDSSAAAAAVVAAAEALALVTAAGREASTLVTEIAAHDAAAEALRARVEAARDAATVAEAAIEADRAALATDSEKVVAALNAHLDGGAGPSSLADVHDDLVEQEELLAAVAVARAADVGATEHLEATRSALATALAAAELADATEARAATLDRTSIQALESSTRLYEQQVAAERATLATPEIAVLPADVDVTSATAALEAAEAALVETRELRDLAVATAATSDGALARARTGAAEVVTAVEGAADVLESTAPVIRIANLADASTADNASRLTLTTYVLARRFDEVLAAANDRLRQMSSGRYELRRSDAKEKGGGQRLGLALRVRDHSTEDDREPTTLSGGETFYVSLCLALGLADVVTAENGGIDLGTLFVDEGFGSLDPETLELVMTELSHLQAGGRVVGVVSHVDAMKQAIADRISVRRRPDGSSTLDVVAGG
>NZ_CP049862.1|WP_166412569.1|69809_70385_+|ATP-binding-protein
MTLSGTCARPGGFPVLWFVGSSGSGKSDASYWTYASLLERSLHVARVDTDDFGMCRPAPADDEPNFRVKAAGLAAMIDVYSAHGAQAVVASGCVNTAAEAALHTDLVPDASWTIVRLHVEPAVRRARLAEREGARQRDDAWIERMVASSLRDDEALDAASFYAHRIDVTGLDRPGVAARVLEVTGWPGPGA
>NZ_CP049862.1|WP_166412570.1|70523_71000_+|M15-family-metallopeptidase
MRFVRRVLAVFILVAVAVGGTQLVKSLTADADSPPAVDADNGRLSQDRLTDIGDGYTLRTDAAKAYAKLRKAARKADVTWSVNSAYRDHDEQVAMVEKFGLLENGGRAAAPGTSEHGLGLSVDLTLEWEEVEWMREHAGAYGFAETIPEEPWHWTYQP
>NZ_CP049862.1|WP_166412571.1|71096_71717_-|3'-5'-exonuclease
MPYAVIDTETTGFSPAKGDRMLEIAVVRLDDAGDVLDTWETLLDPGRGVGATHVHGITAADVVGAPDFGEVAAHVTGLLAGHVVVGHNIDFDLRFLTAELAAVNEPFTLGGKLCTQRLAPDYLPGPKRTLAVCCEQAGIVNDHAHSALGDTLATAELFAFYLRHHRGTPPWASVVAQASRALPADDLFAALTTPPAPRTHTRTLTR
>NZ_CP049862.1|WP_166412572.1|71781_72339_+|hypothetical-protein
MTDDANQPAPRPTARERREAARGVLTEPVISGGPHVDPVRDRQVSVAARTFTLGSVGGAAAGAIGAEAVTVGSGYSGAGLIIGSMIGVVGGLVVAAVATPTVQRAARRHAGRVPLALRLLLAGVSAIGCVLVWWFVARDAIPGEVVLGVVLSAAIAAVAVIVALPWCARPFAPPVATEVSTLPAD
>NZ_CP049862.1|WP_166415119.1|72482_74171_-|amidohydrolase
MPVAAAVAITGERITAVGPDDELRALAGPATRIVDITGRLVLPGFQDTHVHPILAAGMDARLNVLGESDLAGTLGAISAWAAAHPELEWVTGWGWQADHFEGGFPTRQQLDALVPDRPAFLHRSDGHASWVNTRAIELAGLDDDGSGQPPADPAGGYVQRDADGRATGVLIEWATGLVEKHVPDAPLADRLAHLLAGQRALLAQGITAWQDASVRPAEQEVYELADARGELVATVVGALRWEHERGFEQVAKLVERRAEIEARSAARPSRFRPTSVKIMHDGVVDGSLTAAMIDPYLDADGTVSDNRGDSYHSVDDLDRLVAALMAEGFQPHFHAIGDRGVRECLDAVERARAVLASVGVAPGGVTADAHPGVDVGHAPHHDGTGRDVRPIVSHVQVVHPDDRARLAGLGTIVSAQPLWANCEDVQTELTMPFLGEERSAWQYPFASLAAAGALLAGGSDWPVSTADPLQGIHTAVTRRLFGEDRPALYPSEALTLAEAVRMYTYGSAVANHREDESGVVAPGLLADLAIIDRDIFAAPVDEIGEARVVATWVRGVEVHTAP

Crispr_ID: NZ_CP049862_3

• CRISPR_ID: NZ_CP049862_3
• CRISPR_location: 97678-97782
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP049862_3

Consensus_repeat	Method
TCGAGCGGGGTGTCCTCAGTGACCGCG	CRISPRCasFinder

spacers of NZ_CP049862_3

>3.1|97705|51|NZ_CP049862|CRISPRCasFinder
GCGTCGGTGGGCGCACCCCAGATCGTGTCGGCCGGGACCTCGGTGGCGGCG

CRISPR arrays and Neighbor proteins around NZ_CP049862_3

CRISPR arrays

The CRISPR arrays of NZ_CP049862_3

>merge|NZ_CP049862|3|97678-97782|CRISPRCasFinder
TCGAGCGGGGTGTCCTCAGTGACCGCGGCGTCGGTGGGCGCACCCCAGATCGTGTCGGCCGGGACCTCGGTGGCGGCGTCGAGCGGGCTGTCCTCAGTGACCGCG

>NZ_CP049862|3|3|97678-97782|CRISPRCasFinder
TCGAGCGGGGTGTCCTCAGTGACCGCG	GCGTCGGTGGGCGCACCCCAGATCGTGTCGGCCGGGACCTCGGTGGCGGCG
TCGAGCGGGCTGTCCTCAGTGACCGCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP049862.1|WP_166415122.1|106713_107571_+|ArgP/LysG-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|235144
NZ_CP049862.1|WP_166412594.1|107692_108538_+|hypothetical-protein	unknown	unknown	gnl|CDD|237030
NZ_CP049862.1|WP_166412588.1|101056_101533_-|hypothetical-protein	unknown	unknown	gnl|CDD|376684
NZ_CP049862.1|WP_166412580.1|82769_84029_+|rubrerythrin-family-protein	unknown	unknown	gnl|CDD|153124
NZ_CP049862.1|WP_166412577.1|80023_80767_-|HNH-endonuclease	unknown	unknown	gnl|CDD|377857
NZ_CP049862.1|WP_166415121.1|98729_99071_-|DivIVA-domain-containing-protein	unknown	unknown	gnl|CDD|274639
NZ_CP049862.1|WP_166412592.1|104680_105913_-|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_CP049862.1|WP_166412583.1|93591_94248_-|SRPBCC-family-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412578.1|80923_81361_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412590.1|102434_103772_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412593.1|106037_106715_-|amino-acid-transporter	unknown	unknown	gnl|CDD|224198
NZ_CP049862.1|WP_166415120.1|91292_92072_-|AAC(3)-family-N-acetyltransferase	unknown	unknown	gnl|CDD|376807
NZ_CP049862.1|WP_166412579.1|81542_82763_-|DUF2804-domain-containing-protein	unknown	unknown	gnl|CDD|378522
NZ_CP049862.1|WP_166412584.1|94426_95134_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|366102
NZ_CP049862.1|WP_166412581.1|84384_89478_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412587.1|99439_100924_-|flotillin-family-protein	unknown	unknown	gnl|CDD|225177
NZ_CP049862.1|WP_166412585.1|95269_96235_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412589.1|101758_102253_+|hypothetical-protein	unknown	unknown	gnl|CDD|341373
NZ_CP049862.1|WP_166412582.1|92131_93517_+|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_CP049862.1|WP_166412591.1|103768_104566_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213222

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP049862.1|WP_166415122.1|106713_107571_+|ArgP/LysG-family-DNA-binding-transcriptional-regulator	gnl|CDD|235144	PRK03635, PRK03635, ArgP/LysG family DNA-binding transcriptional regulator.	2.34387e-92
NZ_CP049862.1|WP_166412594.1|107692_108538_+|hypothetical-protein	gnl|CDD|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	0.00375576
NZ_CP049862.1|WP_166415121.1|98729_99071_-|DivIVA-domain-containing-protein	gnl|CDD|274639	TIGR03544, cell_division_initiation_protein_DivIVA, DivIVA domain. This model describes a domain found in Bacillus subtilis cell division initiation protein DivIVA, and homologs, toward the N-terminus. It is also found as a repeated domain in certain other proteins, including family TIGR03543.	0.00303039
NZ_CP049862.1|WP_166412580.1|82769_84029_+|rubrerythrin-family-protein	gnl|CDD|153124	cd02433, Nodulin-21_like_2, Nodulin-21 and CCC1-related protein family. Nodulin-21_like_2: This is a family of proteins closely related to nodulin-21, a plant nodule-specific protein that may be involved in symbiotic nitrogen fixation. This family is also related to CCC1, a yeast vacuole transmembrane protein that functions as an iron and manganese transporter. .	3.23818e-66
NZ_CP049862.1|WP_166412577.1|80023_80767_-|HNH-endonuclease	gnl|CDD|377857	pfam07510, DUF1524, Protein of unknown function (DUF1524). This family of uncharacterized proteins contain a conserved HXXP motif. A similar motif is seen in protein families in the His-Me finger endonuclease superfamily which suggests this family of proteins may also act as endonucleases.	2.31076e-14
NZ_CP049862.1|WP_166412589.1|101758_102253_+|hypothetical-protein	gnl|CDD|341373	cd04598, CBS_pair_GGDEF_EAL, Two tandem repeats of the cystathionine beta-synthase (CBS pair) domains associated with the GGDEF (DiGuanylate-Cyclase (DGC)) domain. This cd contains two tandem repeats of the cystathionine beta-synthase (CBS pair) domains in association with the GGDEF (DiGuanylate-Cyclase (DGC)) domain. The GGDEF domain has been suggested to be homologous to the adenylyl cyclase catalytic domain and is thought to be involved in regulating cell surface adhesiveness 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).	2.17173e-09
NZ_CP049862.1|WP_166412588.1|101056_101533_-|hypothetical-protein	gnl|CDD|376684	pfam01957, NfeD, NfeD-like C-terminal, partner-binding. NfeD-like proteins are widely distributed throughout prokaryotes and are frequently associated with genes encoding stomatin-like proteins (slipins). There appear to be three major groups: an ancestral group with only an N-terminal serine protease domain and this C-terminal beta sheet-rich domain which is structurally very similar to the OB-fold domain, associated with its neighboring slipin cluster; a second major group with an additional middle, membrane-spanning domain, associated in some species with eoslipin and in others with yqfA; a final 'artificial' group which unites truncated forms lacking the protease region and associated with their ancestral gene partner, either yqfA or eoslipin. This NefD, C-terminal, domain appears to be the major one for relating to the associated protein. NfeD homologs are clearly reliant on their conserved gene neighbor which is assumed to be necessary for function, either through direct physical interaction or by functioning in the same pathway, possibly involve with lipid-rafts.	1.09804e-06
NZ_CP049862.1|WP_166412593.1|106037_106715_-|amino-acid-transporter	gnl|CDD|224198	COG1279, COG1279, Lysine efflux permease [General function prediction only].	1.81784e-60
NZ_CP049862.1|WP_166415120.1|91292_92072_-|AAC(3)-family-N-acetyltransferase	gnl|CDD|376807	pfam02522, Antibiotic_NAT, Aminoglycoside 3-N-acetyltransferase. This family consists of bacterial aminoglycoside 3-N-acetyltransferases EC:2.3.1.81, these catalyze the reaction: Acetyl-Co + a 2-deoxystreptamine antibiotic <=> CoA + N3'-acetyl-2-deoxystreptamine antibiotic. The enzyme can use a range of antibiotics with 2-deoxystreptamine rings as acceptor for its acetyltransferase activity, this inactivates and confers resistance to gentamicin, kanamycin, tobramycin, neomycin and apramycin amongst others.	7.73606e-60
NZ_CP049862.1|WP_166412579.1|81542_82763_-|DUF2804-domain-containing-protein	gnl|CDD|378522	pfam10974, DUF2804, Protein of unknown function (DUF2804). This is a family of proteins with unknown function.	9.26361e-105
NZ_CP049862.1|WP_166412584.1|94426_95134_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	5.32511e-16
NZ_CP049862.1|WP_166412587.1|99439_100924_-|flotillin-family-protein	gnl|CDD|225177	COG2268, COG2268, Uncharacterized protein conserved in bacteria [Function unknown].	6.2111e-44
NZ_CP049862.1|WP_166412592.1|104680_105913_-|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.	3.1282e-17
NZ_CP049862.1|WP_166412582.1|92131_93517_+|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.	3.91765e-53
NZ_CP049862.1|WP_166412591.1|103768_104566_-|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.	1.27279e-98

Protein sequences

>NZ_CP049862.1|WP_166412585.1|95269_96235_+|hypothetical-protein
MFLFDSIPWYSALMWLLVLGVLIGLNELVRWSKVAAYAVFIVLPIVLTIFVWPTTAAAGSSTGTWFHWVKVYSALAGCIGFMLIRYNKRIAANKYALWFPPAILALNIAEAVIRDFQVAGLQGMHDGVFMVGGAWNYMNGIAGILNLVTICGWVGIFVTKDRFQDMVWPDMLWFWIIAYDLWNFAYVYNCVGDHAFYAGAALLISCTIPAFFLRKGGWLQHRAHTLAFWMMFTMAVPSFVSDSKFAVDASHDPTALFVVSLLSLLANIAVVVYQVRTIIVKRRNPLRDELYTHLAAYQAIAAERPAPDTADAEEAATAPAV
>NZ_CP049862.1|WP_166412584.1|94426_95134_+|TetR/AcrR-family-transcriptional-regulator
MSTDKAPRSPRTAPDVRSDELVAAARELFAEQGLSRTTLSDVARRVGVARTLVYHYFPSKDALVEAVLDGYVEHFVGSVRAWDAARTTGDIEGSLVTAIALFRTHLRAMDPIRPDLERVEATGMYNAFLDRAVRAIVDCLEETTVQAYAARHQIRIDHVRETFYVLVYGLVGLARNTPGIDDALLVALVRQALRLEPDTTVVPETVACASGERPAGAPAPLGQDAPASPEVATEH
>NZ_CP049862.1|WP_166412583.1|93591_94248_-|SRPBCC-family-protein
MARLPSLRALLTTGAVLTALATLPVLRTWAMQWGSTEAELDATLPGDELTPAADHVVTRAVSIDAPPSDVWPWLVQLGTGRGGFYSYDALENLAGLGIRSADRIEPHLQDLAPGDPVALAEGLELRVATLEIDRALVLAGIPEPGDTPEMPFRFSWAFVLEETGGGTSRLVVRERYEYLRRSAALVVEPTTFVSWLMTQQMLRGIRTRAERPLPVPLP
>NZ_CP049862.1|WP_166412582.1|92131_93517_+|MFS-transporter
MPRLLIDTSPLRESPAFARMWWGLGLSSLGTQLTVVAVGLEVYDITGSTLAVGGLGIAALVPLIVTGLYGGALVDVHDRRKVALTTSAGLWIVTALLALQAWLQVDEVWVLYALVALQSAGFGINNPARSAIIPMLVPPSRLPAANALQTLLFNTSLMLGPVAGAVLVARWGYEVAYTIDAVLFLAALWALVRLPSLRPGTIAYATEPGGGPARDVVVPVASVPDSTSVDVPDPDVAPARRRVGLSSVVEGLRYLATQPNVRMTFLVDLAAMVLAMPRVLFPALGVVVLGGGETTTGYLTAAIGVGGIAAGLLSGGLVRMWRQGAIIVWAITAWGLGVAGFGAVLLGAGRTTPDHVLWPALAAALVLLAFCGAADNVSAIFRTSILQTAVPDEMRGRLQGIFIVVVAGGPRAGDLWLGAQASWWGEGMAAVVGGLTCVTVLWLLTRRWPAFYKYDAHHPTP
>NZ_CP049862.1|WP_166415120.1|91292_92072_-|AAC(3)-family-N-acetyltransferase
MTSLTRARLADDLRTLGLRPGDDVLVHSSLRGLGHVEGGASSVVDALLDAVGPGGTVLFPTITATAEHGPAHPPRVVLAATPGWTGAIPEAARVRPDSVRSVHPTHSVVALGARARELTDGHASSATPCDASSPYGRLADRGGRVLLLGGVTHSSSTSLHGVEERAAVPHHLQDEPTDGVVVLPDGTEVVVRGRLHQWGWDRDFERVADPLRAAGVQLDGRVGAGAAILVEARGYVDVLVPLLLTDPTYLLAEHERTRA
>NZ_CP049862.1|WP_166412581.1|84384_89478_+|hypothetical-protein
MAWLPDPTGRTALRLEENGAWTSWVSDGRQSWQDPRPVRRILGQGDAAALAFVTDVFLPEAWAAGALDPARARALETVVGMLRAETTAPAVGVVPAPAASPAMSAAPTAQPGMQSTLQMPTAPFAPPTASPTMQPTMQPAVQPVTQPAFPPGAAASGYVPGTIRMRPVEHPSAAYGPRRDPAVPRTPRPAPAWRRALAASLAAHGLAYLGVLLLFVGVFGLVAFAFGDVSPALRPVAELTAAAVPFVAAWRLRRAGAADVAQALVVLGGLLVPLLLVTSLVDGFRVPPDPRGAPLVVALTLVPLACAIAYVVRARRVPGSALRHVVVPSLVLAAAMATTGVGRPMPVGQDVAEPSAWQAGAMALALAVVLVVARVRSVRVGPSGPATLVVVTVLAMLTWAAGAPAAWLVLATGAGLVVALLAVRTTLPASLTDVAAPLAWGVTALVAGNVEARLAVPALLVVVVAAGFLALVEDAGRRGRPTVVLGLPVVGLGAAMLAAVPEPSAATGLCAIVTAWALARRAWPFPASPQGVRHLIGVVAGLAPAFGLVMLGVATRPTLALGVAVVVLGAGLVPARRSEAARGTTGVDGYWRAWWRSGLALVAAAVPGVQLWASVAETATPADRWVRVAVLVALAVLVGLGPLAPALRVWLAAVFGTWAWFGVVGLTGAPVVVGAGVIALAALVLVVVARPRPVAMVGQALVCVAFVPIAVVRLASEVGGADPDGTLTWALAAVLAAATATSVVAAVRAERRAPRTGLSDVVLSDGAVLDGTVSRRAALDGAAPSAPVSDATPPHGVGLAATGPMRATTPPTLLDPRAPWLCVVLGVPATLLVTLHAVIGSAGVEVPGWTAAVVVGAWALCLAALANLLRPEPTGRIALRGAADLAPWSAGLLGVLAVGLSTGTSYGESGTQDWWPAAPADRWVEVAMLAVVALVPVVLPARLRPRALVVLAWAALPVLVLRASGAASGWVREHPAEATAVVATAIGASYVLAVAVASPRRAWPTRPAARPPFVVGTTLLGVAALLAVATPAGPSNAGSVTLPSGLVLPAGLGQVLGTSVLAAVAAVLLVVAWRCRSPWHVTAGTVIAWCAGLLALPDLVAGHPWVAILAGLLVVLAAEVTYRRTPLARRRHLALLVAAPPIALTALTWRAPEHLALGGLAVLVALVLALRGGRAAADAVALGGVIVAALALDSGLWGPAVAAGLLALAATGLALVTRNAVRGVVGAAAGLVAWALAVLAAGLTAQAVAELSLVVGAAVATAVGAAWSVVERRRGAASRQPAEPTADSDEARALGPTQPLLSPSAGARAALRPVVRAWWAAAILVAGVGAVTALTGAVTVGWPIVGGGALVVVALGVGVLVWRERILLDAAAVALALTVLAACAASGAGASVRIIVLSGLAAAAAVVAAGVAVLARGSRRPRLPRVLAAHGPRALAVGSLATILLALAVVVPLVPGQAEGDGGLAGRLAVVLVALAVQLGAWGVARRSLAAQVLSPLAAALAWLVLAPGLSADVAWSAVPLGLALLVDASLLREDRRRRSVPRVEARAVAPTGAAGVPRPAAGMRPSAVGRSAAPELALELLGLAFVIGPFVVRTVEQSVAWAAVVLLVGALTVAWGVLTKVRRRLVSGAAIALGAVVLLVGVPLVALVPAWGDAGAWLLVAGVGAVAVVGATVLEKGRSAVSGLWLRLGSDDGGWE
>NZ_CP049862.1|WP_166412580.1|82769_84029_+|rubrerythrin-family-protein
MPDALPDAVLPATDPSARDVRRWRHHLADELAEAAIYRDLAAARTGAERDILLELADAEGRHAEHWRELLGPERAASVRRSPYSRLLGIGARRFGSVFTLALAQHAESRSAYELDRDATPQMAADERIHEEVVRSLATRGRIEMSGNFRAAVFGLNDGLVSNLALILGIGATGVGTGTVLATGVAGLLAGAMSMGAGEFVSVRSQVELANASQPSPRAREALVHLDVDANELALVYRARGLDAAAADARARRTLELVARADAAEAAAVQDDGAALGGVPAIAGAGAGAGAGAGSGADAAAVDDAVGEALDVPAAADAVDATGPDAELLGSAWGAAISSFFLFASGALVPLLPYLLGMSGGAAMILAAVLVGAVLLGTGAIVGVLSGASPWTRALRQIAIGYGAAAVTYVLGLAFGTTLG
>NZ_CP049862.1|WP_166412579.1|81542_82763_-|DUF2804-domain-containing-protein
MVASAPRLVSARGDVGARTPGRGSVETRRAPEVRGCSQPGRRRPVRKEEHVPQVEREITTPVRLVGPRGRLDPAAHGWSRTPLHDTTLPVGPRFWGRNKRWEYWGLVTPTHIIGLTISNLDYAAVHQLYVLDRRSGDTVDAAVTNPLGRGTVLPELLAQGPSRASGRRFDLAIDDVAPAVDDDVTVSGLAVPPDAPRPGRATRLRARTPRVELDLVAERRPGWEAMCVVVPFGPGRYQYTVKDVAIPLRGTLVIDGEHLEVGDDAWAVLDHGRGRWPYSRTWNWAAGSGMVDGVRTGLQLGGRWTVGTGSTENALVLDGVVHKISEEVAWEYDRDDWMRPWRVHGEQVDVTFTPFHERRAVTNLVVLAGDTTQCFGTWEGWMSTTDGERVRVDGLVGWAEEAKNRW
>NZ_CP049862.1|WP_166412578.1|80923_81361_-|hypothetical-protein
MSEVLVRENSGAHMMRPVMWAAVSVLGLEAVTGLVGVSVLSYRAVTTAGFAGHTGGDVLSRTFVIVLLLALVGAAIAMGVAMVRHRRRGGAPSRPLVLAAITVLITHALIIVGCLVRAEWATATAIAVGAVVLGSAWAHCLRRHR
>NZ_CP049862.1|WP_166412577.1|80023_80767_-|HNH-endonuclease
MPQHRSPAARRPRTRGPALVALASVVLLALAWWASEPWRAPARTYPVTTADLVSARAALATLPELAEEPPTQYSRERFGTPWADVDGNGCSTREDVLARDLAEARTDDDGCTVLAGTLDDRYTGRVLPFRRGPTTSARVQIDHVVALADAWRTGAWDWDDARREQLANDPANLLAVDGPTNEDKGAQDASTWLPPYAPFGCQYAVLRLQVRAAYGLALVPGERGALERALGRCEVAEITVTGEALRH
>NZ_CP049862.1|WP_166415121.1|98729_99071_-|DivIVA-domain-containing-protein
MLLGARTHEASRLVAVAGEGGPFARLAERAVRVRFSRSGWGGGYEIEAVDTLVTHIVTTAVARDQRRSTTPDGTPLLTGVGVRTTVLPRVRFRPGYSTTEVDAFLQEVAGVLG
>NZ_CP049862.1|WP_166412587.1|99439_100924_-|flotillin-family-protein
MPPSSTDPNFWTVVGVALLAIAFLAIVTFIAKRIRRVPPNEALVIVGRGAGKNQPDMIGGQRVVVGGRVFVWPILQQGFPISLEQRQIGITVEGVDKNRVKIAIKASINFKVRGDDDGVRRAAQRFLSQQDALTEIIKESLEGSLRSIVGDMTIEQIISDRKGLSDRVVDSTKTDLAEQGLQVDLLNISDISTPGSDYLANLGRAENARARQVAEVSEAEARRIAEFAVIDAAEQIAERQKALDLKKATIKAETDRANAEADAAGQLARVEQERLVALEQREALTEQAKVTEEELDISVRKPAEADAYAAVQKANAERDAANAATEADAFKRTTIAQANKTAAIQDAEAAAEAVRRAGEGERDRQVALAAGIRAEGEARAAATEAEGRAEAAATDAKAEALKKYGEAALAQELITRLPEIIRAAAEPMGAVDRMTVISTDGASALTKNITGVLSEGQQIVKDLLGIDLSSLIGGVAGGALLPKKDDAKDAAPSA
>NZ_CP049862.1|WP_166412588.1|101056_101533_-|hypothetical-protein
MTVFVIIGVVGLLLVIGSMLLGEFIELGDGALSSTGLGVGAIVFGAIGIMTTANDLPTGLVYGGSAVAGIAAVWLSQLAIKRLQATEDGQPLKLVGMTGVAKSDITTQRGEVFLDTPQEIERRMAWSDAPIAEGSRIVVVAQEGSRVKVAPGDGAPTA
>NZ_CP049862.1|WP_166412589.1|101758_102253_+|hypothetical-protein
MITRTIAPHVDGRRRETAIDRLDDPFVPVGRLAIPIEVVDSTTLYPGVAALFRSENVSSVAVCDSTDPRRIGLISRDRHTAVSAGTLGYGRALLARRQVGEVVDWGPLAVPQAMPVVEVVRHAMARPEARRFDDVVVHGAVWQVVTVPTLVRALADAVTTRWHG
>NZ_CP049862.1|WP_166412590.1|102434_103772_-|hypothetical-protein
MRALGLWWFLRRRTTDARDPQRLSTVLAVVAFAFSTAALLVVAGGYGAFVDRAAAPGGSPDADQYPLLAGVASLLLLVPLTTLGGAAARLAVARRDERLATLRLAGATTGQVTTFTTLDAAAQALVGAVAGVALYCALLPAVALLNFQDRRFEIAELWVGVPLVLAAVGLVVVIALVSALASLRRVAVTPLGVAARTTPPGLRAVRALVLVAAVVAMPVVVNVPFGGDGVAIAMIVGVLVLGFAALGAIGPFVLQLVGRVTVRRARSVETLLAGRRIVDDPRTAWRSVGGVALATFIAGLASITALFTPPADADPWEIVFTADLRTGALLTLAIAGILAAVSTGVMQAGRAIDQREQSGALILAGSEPRTLDRARMRETTIPLAASVGLATATMLMLIAPVLGLGAFQQVSVVVELLAAIAAASALVGAGAWAAGLVARRTLPTP
>NZ_CP049862.1|WP_166412591.1|103768_104566_-|ABC-transporter-ATP-binding-protein
MNARSSDRLVARGLTQVYGDGPFATHALDGVDLTVEPGESLAIMGPSGSGKTTLLHVLAGILAPTSGSVAWRGEDLAALPDRRRTQLRRTDFGFVFQSGRLLPELPAVENAALPLLLAGMPRAQAVATAAAELGRLGLRGLEGRRPGELSGGQAQRVAIARALVGRPGIVFADEPTGALDQATGQEVLTVLTAAAAANGAALVVVTHDAGVAQHCERTVTMRDGRIDGEFFAAARSAAAPVAAAPVAPVPLPPGALPATPAGGAR
>NZ_CP049862.1|WP_166412592.1|104680_105913_-|MFS-transporter
MAIGGPYRAILARPGAAQFSISGVISRFPMAMVGIGIVLMIEGLHGSYALAGRVSAVYVLAQAVCGPQIARLIDRYGQARVMRPLLAISASGISGLVVASVLDAPAWALYVIAALGGSTIGSMGTLVRARWSKLVGGNPHELHTAYSLEASLDEVVFVIGPVLATWLATSVTPWAGIVFPVVAMLVGGYWFLSLKDSEPVPTPQTREERQPTVLRFGAMVSLVLVFVALGGVFGATDVATIAFAEEHGNKGAAGVILAVFACGSLVAGLWYGVRRWVTPLWVRFVVTMLGLAGGVAFFPLVDSLWALAGLMFFTGLMIAPSLIGGNGLVQLVVPQTQLTEGLTYVGTALGVGVSLGSSIAGSRIDAAGAHAGFIVAIIAAGLGALLVVASAPVLRRSSTRRSGDVEVAAH
>NZ_CP049862.1|WP_166412593.1|106037_106715_-|amino-acid-transporter
MKNCFTAYRLSRSPSHPSGAYRRPVTTTLTALTTGFLASLGLIVAIGAQNAWVLRQGLRREHVGLVVAICVGADVVLMAAGTAGLGVLRDAAPWALEVLRWGGVAYLLFFAAMSLRSALTSREHLEASAARPARSVALTTLAVTLLNPHVYLDTLVMLGTVTNSFGDLRWVAAGGAMVASLVWFTLVGLGARALSGVLDRPATWRVIDGVVAVVMVVVAAMLAFG
>NZ_CP049862.1|WP_166415122.1|106713_107571_+|ArgP/LysG-family-DNA-binding-transcriptional-regulator
MSPEQLAALAAIDDEGSFEGAAYELGVSTSAVSQRIRTLEASLGRILVRRGTPSTVTPDGAPVLRHARQQALLAAELADELGGVPAGTGPVPLAVAVNADSLATWFRGVLVAAGAWTDTFLQVVADDEGHAVERLRSGAVMAAVATDPTPAPGCRAERLGVVRYSPRVHPDLLARHDVRGPADVPRLPAVRFDTKDGLQDLALEAAGQPRAGRGPAVPSPDGFAAAVRAGLGWGMLLDPQVADAPELVPVPGLAPVERELFWQRWTIGSHRLDRLTDAVREAFPG
>NZ_CP049862.1|WP_166412594.1|107692_108538_+|hypothetical-protein
MRTRTILVTAVAAAAMLAGCSDGPGPTASGDPSSTGSAPQAGAAGTPSATPGGTAPSATPSDAATEVPAASREVPAECASLALAGGATYSGEALGACVAEALPSYGSGRMRMFGDDLDGTVAFTYTPAYSFSVEGKNAGDTIRMTYNDGEVWVDQGDGPVRGDVKSEKQEEMLAGFVAEMYRSYSDPAMYADLVRSSKGWTADAGTKAVELPDGSSVDSFRIVSDKPFTWHDAPVDEYVLEFGADWVPVSAAATMSVLGQSSTVTQHFYDLGTDITITPLG

Crispr_ID: NZ_CP049862_4

• CRISPR_ID: NZ_CP049862_4
• CRISPR_location: 111665-111754
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP049862_4

Consensus_repeat	Method
GAGCACCGTTCGATGGTGCTCCGGACCT	CRISPRCasFinder

spacers of NZ_CP049862_4

>4.1|111693|34|NZ_CP049862|CRISPRCasFinder
CCGAGTCGTTCCGGGTGTGCGACTCGTAGGGTGC

CRISPR arrays and Neighbor proteins around NZ_CP049862_4

CRISPR arrays

The CRISPR arrays of NZ_CP049862_4

>merge|NZ_CP049862|4|111665-111754|CRISPRCasFinder
GAGCACCGTTCGATGGTGCTCCGGACCTCCGAGTCGTTCCGGGTGTGCGACTCGTAGGGTGCGAGCACCGTTCGATGGTGCTCCGAACCT

>NZ_CP049862|4|4|111665-111754|CRISPRCasFinder
GAGCACCGTTCGATGGTGCTCCGGACCT	CCGAGTCGTTCCGGGTGTGCGACTCGTAGGGTGC
GAGCACCGTTCGATGGTGCTCCGAACCT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP049862.1|WP_166412602.1|122298_123273_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP049862.1|WP_166415123.1|111976_112738_+|glycosyltransferase	unknown	unknown	gnl|CDD|133022
NZ_CP049862.1|WP_166412597.1|110785_111616_+|topoisomerase-II	unknown	unknown	unknown
NZ_CP049862.1|WP_166415122.1|106713_107571_+|ArgP/LysG-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|235144
NZ_CP049862.1|WP_166412601.1|119709_121125_+|carbohydrate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|224567
NZ_CP049862.1|WP_166412595.1|108630_108909_+|N-acetyltransferase	unknown	unknown	gnl|CDD|379642
NZ_CP049862.1|WP_166412589.1|101758_102253_+|hypothetical-protein	unknown	unknown	gnl|CDD|341373
NZ_CP049862.1|WP_166415125.1|117705_118464_+|HAD-family-phosphatase	unknown	unknown	gnl|CDD|369792
NZ_CP049862.1|WP_166412598.1|112800_114990_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412590.1|102434_103772_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412593.1|106037_106715_-|amino-acid-transporter	unknown	unknown	gnl|CDD|224198
NZ_CP049862.1|WP_166415127.1|123454_124468_-|NAD(P)H-quinone-oxidoreductase	unknown	unknown	gnl|CDD|176180
NZ_CP049862.1|WP_166412599.1|116287_117577_+|serine--tRNA-ligase	unknown	unknown	gnl|CDD|235461
NZ_CP049862.1|WP_166415126.1|121366_122302_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP049862.1|WP_166415124.1|115050_116157_-|diacylglycerol-kinase	unknown	unknown	gnl|CDD|224513
NZ_CP049862.1|WP_166412596.1|108998_110681_-|alpha-D-glucose-phosphate-specific-phosphoglucomutase	unknown	unknown	gnl|CDD|236050
NZ_CP049862.1|WP_166412600.1|118513_119536_+|LacI-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_CP049862.1|WP_166412592.1|104680_105913_-|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_CP049862.1|WP_166412594.1|107692_108538_+|hypothetical-protein	unknown	unknown	gnl|CDD|237030
NZ_CP049862.1|WP_166412591.1|103768_104566_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213222

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP049862.1|WP_166412602.1|122298_123273_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	6.73025e-77
NZ_CP049862.1|WP_166415123.1|111976_112738_+|glycosyltransferase	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.	6.42538e-20
NZ_CP049862.1|WP_166415125.1|117705_118464_+|HAD-family-phosphatase	gnl|CDD|369792	pfam08282, Hydrolase_3, haloacid dehalogenase-like hydrolase. This family contains haloacid dehalogenase-like hydrolase enzymes.	9.98509e-38
NZ_CP049862.1|WP_166415122.1|106713_107571_+|ArgP/LysG-family-DNA-binding-transcriptional-regulator	gnl|CDD|235144	PRK03635, PRK03635, ArgP/LysG family DNA-binding transcriptional regulator.	2.34387e-92
NZ_CP049862.1|WP_166412601.1|119709_121125_+|carbohydrate-ABC-transporter-substrate-binding-protein	gnl|CDD|224567	COG1653, UgpB, ABC-type sugar transport system, periplasmic component [Carbohydrate transport and metabolism].	1.07986e-23
NZ_CP049862.1|WP_166412595.1|108630_108909_+|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.	5.25682e-23
NZ_CP049862.1|WP_166412589.1|101758_102253_+|hypothetical-protein	gnl|CDD|341373	cd04598, CBS_pair_GGDEF_EAL, Two tandem repeats of the cystathionine beta-synthase (CBS pair) domains associated with the GGDEF (DiGuanylate-Cyclase (DGC)) domain. This cd contains two tandem repeats of the cystathionine beta-synthase (CBS pair) domains in association with the GGDEF (DiGuanylate-Cyclase (DGC)) domain. The GGDEF domain has been suggested to be homologous to the adenylyl cyclase catalytic domain and is thought to be involved in regulating cell surface adhesiveness 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).	2.17173e-09
NZ_CP049862.1|WP_166412593.1|106037_106715_-|amino-acid-transporter	gnl|CDD|224198	COG1279, COG1279, Lysine efflux permease [General function prediction only].	1.81784e-60
NZ_CP049862.1|WP_166415127.1|123454_124468_-|NAD(P)H-quinone-oxidoreductase	gnl|CDD|176180	cd05276, p53_inducible_oxidoreductase, PIG3 p53-inducible quinone oxidoreductase. PIG3 p53-inducible quinone oxidoreductase, a medium chain dehydrogenase/reductase family member, acts in the apoptotic pathway. PIG3 reduces ortho-quinones, but its apoptotic activity has been attributed to oxidative stress generation, since overexpression of PIG3 accumulates reactive oxygen species. PIG3 resembles the MDR family member quinone reductases, which catalyze the reduction of quinone to hydroxyquinone. 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.	2.60998e-130
NZ_CP049862.1|WP_166412599.1|116287_117577_+|serine--tRNA-ligase	gnl|CDD|235461	PRK05431, PRK05431, seryl-tRNA synthetase; Provisional.	0
NZ_CP049862.1|WP_166415126.1|121366_122302_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	3.41824e-63
NZ_CP049862.1|WP_166415124.1|115050_116157_-|diacylglycerol-kinase	gnl|CDD|224513	COG1597, LCB5, Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase [Lipid metabolism / General function prediction only].	3.14986e-37
NZ_CP049862.1|WP_166412596.1|108998_110681_-|alpha-D-glucose-phosphate-specific-phosphoglucomutase	gnl|CDD|236050	PRK07564, PRK07564, phosphoglucomutase; Validated.	0
NZ_CP049862.1|WP_166412600.1|118513_119536_+|LacI-family-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	2.62695e-102
NZ_CP049862.1|WP_166412592.1|104680_105913_-|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.	3.1282e-17
NZ_CP049862.1|WP_166412594.1|107692_108538_+|hypothetical-protein	gnl|CDD|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	0.00375576
NZ_CP049862.1|WP_166412591.1|103768_104566_-|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.	1.27279e-98

Protein sequences

>NZ_CP049862.1|WP_166412597.1|110785_111616_+|topoisomerase-II
MAKNSSPALVLRPFENLPGEADWVALREIVPAATATVRTTAEHGARDVVVTTSLPDGWPALHRTDGTVLLALQNVLGGGDLSRTLAANLLAILDSEPGTSLTHVESPADDAPRLQDVLDPSVPFTVTLHDGFDYWFGADQTIDGDLRKALDDAAETIIPTEPLAGVDSAYLATFGKRRYLRWSMAVDEDRLVDGVARLHAKRESALGKSRFLGIFRACGIVVPVWDVADGATLEEIETLAEEMRPRLEAAIASSEPLTSDERRARAGIVARQVSLR
>NZ_CP049862.1|WP_166412596.1|108998_110681_-|alpha-D-glucose-phosphate-specific-phosphoglucomutase
MHPRAGTVALPDDLIDVDALLAAYYDRAPDLDDPAQRVVFGTSGHRGSSLDGAFNEAHIVATTQAIVEYRRSQGTDGPLFIGRDTHALSEPAFRSALEVLAANDVEVRVDARDSWTPTPAVSHAILLHNGATTAAGVVTHGPGLADGIVVTPSHNPPRDGGFKYNPPHGGPADSDATKIIAARANEILAQGVGQVRRVSYEAALAAPTTRKHDYLSAYVDDLGSVLDLDAVRSAGVRIGADPLGGAAVEYWGAIGERYGLDLSVVNPHVDPRWAFMTLDWDGKIRMDCSSPNAMASLVHTMRPAAGGAAPYDIATGNDADSDRHGIVTPDAGLMNPNHFLAVAIDHLYGGARPGWRPDAAIGKTLVSSALVDRVAGGLGRRLLEVPVGFKWFVPGLLSGEVGFGGEESAGASFLRKDGTVWSTDKDGILLALLASEIQATTGKSPSQRHAELVATYGESWYARVDAAATLEEKATLGALDPAQVRSTHLAGEEITAKLTAAPGNGAAIGGLKVTTENAWFAARPSGTENVYKIYAESFVSAEHLTQVQEEAKQVVADALG
>NZ_CP049862.1|WP_166412595.1|108630_108909_+|N-acetyltransferase
MEITVVHDPDLELFEARSSAGDRVGDVTYRRDGDVWDLVGTHVPPELGGRGIASAMLRDVLAQIRAVDGKVRPTCPFVVAYLDRHPDEATRV
>NZ_CP049862.1|WP_166412594.1|107692_108538_+|hypothetical-protein
MRTRTILVTAVAAAAMLAGCSDGPGPTASGDPSSTGSAPQAGAAGTPSATPGGTAPSATPSDAATEVPAASREVPAECASLALAGGATYSGEALGACVAEALPSYGSGRMRMFGDDLDGTVAFTYTPAYSFSVEGKNAGDTIRMTYNDGEVWVDQGDGPVRGDVKSEKQEEMLAGFVAEMYRSYSDPAMYADLVRSSKGWTADAGTKAVELPDGSSVDSFRIVSDKPFTWHDAPVDEYVLEFGADWVPVSAAATMSVLGQSSTVTQHFYDLGTDITITPLG
>NZ_CP049862.1|WP_166415122.1|106713_107571_+|ArgP/LysG-family-DNA-binding-transcriptional-regulator
MSPEQLAALAAIDDEGSFEGAAYELGVSTSAVSQRIRTLEASLGRILVRRGTPSTVTPDGAPVLRHARQQALLAAELADELGGVPAGTGPVPLAVAVNADSLATWFRGVLVAAGAWTDTFLQVVADDEGHAVERLRSGAVMAAVATDPTPAPGCRAERLGVVRYSPRVHPDLLARHDVRGPADVPRLPAVRFDTKDGLQDLALEAAGQPRAGRGPAVPSPDGFAAAVRAGLGWGMLLDPQVADAPELVPVPGLAPVERELFWQRWTIGSHRLDRLTDAVREAFPG
>NZ_CP049862.1|WP_166412593.1|106037_106715_-|amino-acid-transporter
MKNCFTAYRLSRSPSHPSGAYRRPVTTTLTALTTGFLASLGLIVAIGAQNAWVLRQGLRREHVGLVVAICVGADVVLMAAGTAGLGVLRDAAPWALEVLRWGGVAYLLFFAAMSLRSALTSREHLEASAARPARSVALTTLAVTLLNPHVYLDTLVMLGTVTNSFGDLRWVAAGGAMVASLVWFTLVGLGARALSGVLDRPATWRVIDGVVAVVMVVVAAMLAFG
>NZ_CP049862.1|WP_166412592.1|104680_105913_-|MFS-transporter
MAIGGPYRAILARPGAAQFSISGVISRFPMAMVGIGIVLMIEGLHGSYALAGRVSAVYVLAQAVCGPQIARLIDRYGQARVMRPLLAISASGISGLVVASVLDAPAWALYVIAALGGSTIGSMGTLVRARWSKLVGGNPHELHTAYSLEASLDEVVFVIGPVLATWLATSVTPWAGIVFPVVAMLVGGYWFLSLKDSEPVPTPQTREERQPTVLRFGAMVSLVLVFVALGGVFGATDVATIAFAEEHGNKGAAGVILAVFACGSLVAGLWYGVRRWVTPLWVRFVVTMLGLAGGVAFFPLVDSLWALAGLMFFTGLMIAPSLIGGNGLVQLVVPQTQLTEGLTYVGTALGVGVSLGSSIAGSRIDAAGAHAGFIVAIIAAGLGALLVVASAPVLRRSSTRRSGDVEVAAH
>NZ_CP049862.1|WP_166412591.1|103768_104566_-|ABC-transporter-ATP-binding-protein
MNARSSDRLVARGLTQVYGDGPFATHALDGVDLTVEPGESLAIMGPSGSGKTTLLHVLAGILAPTSGSVAWRGEDLAALPDRRRTQLRRTDFGFVFQSGRLLPELPAVENAALPLLLAGMPRAQAVATAAAELGRLGLRGLEGRRPGELSGGQAQRVAIARALVGRPGIVFADEPTGALDQATGQEVLTVLTAAAAANGAALVVVTHDAGVAQHCERTVTMRDGRIDGEFFAAARSAAAPVAAAPVAPVPLPPGALPATPAGGAR
>NZ_CP049862.1|WP_166412590.1|102434_103772_-|hypothetical-protein
MRALGLWWFLRRRTTDARDPQRLSTVLAVVAFAFSTAALLVVAGGYGAFVDRAAAPGGSPDADQYPLLAGVASLLLLVPLTTLGGAAARLAVARRDERLATLRLAGATTGQVTTFTTLDAAAQALVGAVAGVALYCALLPAVALLNFQDRRFEIAELWVGVPLVLAAVGLVVVIALVSALASLRRVAVTPLGVAARTTPPGLRAVRALVLVAAVVAMPVVVNVPFGGDGVAIAMIVGVLVLGFAALGAIGPFVLQLVGRVTVRRARSVETLLAGRRIVDDPRTAWRSVGGVALATFIAGLASITALFTPPADADPWEIVFTADLRTGALLTLAIAGILAAVSTGVMQAGRAIDQREQSGALILAGSEPRTLDRARMRETTIPLAASVGLATATMLMLIAPVLGLGAFQQVSVVVELLAAIAAASALVGAGAWAAGLVARRTLPTP
>NZ_CP049862.1|WP_166412589.1|101758_102253_+|hypothetical-protein
MITRTIAPHVDGRRRETAIDRLDDPFVPVGRLAIPIEVVDSTTLYPGVAALFRSENVSSVAVCDSTDPRRIGLISRDRHTAVSAGTLGYGRALLARRQVGEVVDWGPLAVPQAMPVVEVVRHAMARPEARRFDDVVVHGAVWQVVTVPTLVRALADAVTTRWHG
>NZ_CP049862.1|WP_166415123.1|111976_112738_+|glycosyltransferase
MARTPRPSTEAARGRQRVAVVIPAKDEARRIAATVRAARAIPYVDMVLVVDDGSVDDTQHVAREAGAVVVRHPHNRGKAAAMETGASVVAMRDAADRPPRLLLFLDADLGETAVNTAPLITPVLKGAADMSIALLPPQPGAGGRGIVVGAARRAIASLTGWTPTQPLSGQRCLTREAFEAATPLARGWGVETGMTIDLVRQGYVAVEVPCELRHRASAKDLKGNIHRAAQYRDVLLAVNARKVKSVFRRAPHA
>NZ_CP049862.1|WP_166412598.1|112800_114990_-|hypothetical-protein
MRALLLSVLAAGLVALPATAAQAAPASAAPGPDVVLVGTTGLQWEDVDPRTTPALHDLATRGALGSTVVRSLRSFTCPADGWLSVSSATRAVDADLAADPADAELLPFGSCRALTGPGADRRIPAWDVYTSVDARGSYGAVPGTVGDALAAAGRTTAALGPGAAIALAGTDGLLDGSYAPVDPADPAALTAATADALTHADVVVVDLGDVRGTTPAERTTSLARVEQAATAVRDALDSTSREAGTSTTLLVASVADGFTAPRLQIGAASGPGVGSPAAGSTLTSPSTRQPGYVITADWARTLLAVAGADAGVRTTGAVVAATGPGRPAAQAIAALRDESLRTVEVRSLTSPHYVGYALLVIAPIVLAGILVRRRPLAGSSPRTARLLHTAALVGASVPLAATLAPLVPWWRTQIPWLTLVGVVVVLASATAALASTRPIARAPLGGAGLVAGLTTLVLLADVVTGSRLQLNGVIGTQALVAGRFYGVNNTTFALLAATTPVVGVALAAPFVARGRRRLGALVVGLVGLVVLVVDGLPSLGADFGGPPALVPGIAVTMLIVAGVRLTWRRIVAVLGSGALVVSLFALADWLRPAAARTHLGAFVQQVLDGEGLDVVARKLSQNVGGLFTSPLALVGVLVGVALLWAGFRWHVFPTEPVREAVAVQPLLGAALAGASTSLVLGFAVNDSGILVPLVGLALLVPLVLVTWTRHLDEVALAGAAADDAATPEA
>NZ_CP049862.1|WP_166415124.1|115050_116157_-|diacylglycerol-kinase
MSGWEIFWIVLAVGLAAGAFALSLLTWRSRHLAHRPHLAVTSPPVPDAPRRLVAFVANPSKPDVAQLRAPVEKACRSLGLEPLWLETTVEDPGSGQARAALEAGAEVVVAAGGDGTVRAVATTLQGTGVPMGLLPVGTGNLLARNLDIPVTDLARSLEIALEGRDRAIDVAWLRVTDAPAGDDAAEVGSEHIFLVIAGIGFDAAMIADTDTTLKAKVGWIAYFLGGIRHLHGRRLEARVLLDDTRRSSMKLRTLLVGNCGRLPGGITLLPDALLDDGILDVAAIDTRAGVAGWAQLFGEVVMQGLGVQPLATNRIGRIDHTQCRSIAVRVPDGAQAQVDGDPVGRATAIECRVDHADLLVRVPRALTL
>NZ_CP049862.1|WP_166412599.1|116287_117577_+|serine--tRNA-ligase
MIDLKLLRDQPDVVRASQVARGDDPALVDAVLDADALRRSSLAEFEELRAEQKAHGKKVAQAASPEERAELLRHTKELAENVKAREAEANAAGARLDELLMRISNVVLDGVPAGGEDDFVVVKEVGTPRDFAAEGFEPRDHLALGEMLRAIDTERGAKVSGSRFYYLTGIGARLELALLNAAVAKALEHGFTPMITPTIVNPEIMRGTGFLGAHADEIYYLGADDQYLVGTSEVALAGYHSNEVVDLSEGPLRYAGWSACYRREAGSYGKDTRGIIRVHQFHKVEMFSYARIEDAEAEHARLLALEEEMLALVDLPYRVIDTAAGDLGSSAARKFDCEAWLPTQQRFLELTSTSNCTTFQARRLGVRERVERDGRSEMRAVATLNGTLATTRWIVAILENHQLPDGSVRVPEGLRPFLGGLEVLTPAGA
>NZ_CP049862.1|WP_166415125.1|117705_118464_+|HAD-family-phosphatase
MSEDGFVSAELRRAVALLRAEGHHVVLATGRPLVALLPVAAELGLVGTPLVAANGSATAVLREDGSFRLTDAVTFRPERALDVLLARMPATFFAVEEVGVGYWVGADFPEGTIMGRQKVVDLALLEGVETTRICAVDAGEHDPRLDAELALLGLDIVHFTIAGTRWLDVAPHGVTKASALEDLRVRLGVRADATVAVGDGGNDVEMLGWAAQGVAMGHATADVVAAADRVTGPITDDGAVPVLHDVLVAGRG
>NZ_CP049862.1|WP_166412600.1|118513_119536_+|LacI-family-transcriptional-regulator
MARGIEDVAREAGVSTATVSRALRGMPNVTEATRVRVEEAARRLGYRPSPSAAALATGRTRTIGLLTPWINRWYFSNVIEGAERRLRAAGYDALLYSFAVSAHGRTSQVDPEVLRRRVDGILVVGLPLDPAEVQALEALEVPIVFVGTGRGDHPVVGIDDVGLARAATEYLMGLGHRRIGHITGTPDDLRSWTPPEDRRQGWARVLRDGGIDAEDSWAEFGFFDIEGGTVSTHRLLDRHPELTALFVASDEMAMGAMLAARERGLRVPEDLSIVGVDGHDIAELVGLTTMAQPVVQQGSAAAGIMLGLIGAEPAGPAPDAGAVMFPTTLVVRTTTAAPPV
>NZ_CP049862.1|WP_166412601.1|119709_121125_+|carbohydrate-ABC-transporter-substrate-binding-protein
MSTRKSTIAVSAIAASLLLALSACAPDPADPGKTTGTGTGTGSAAPTADVKPGCEDYAVYGDLSGKTVSIYTSIVELEGEDQKESYKQFEECTGATIDYEGSREFEDQLPIRIEAGNAPDIAYLPQPGLLKTLVANYPGKVIAASEGTAANVDKFFSPSWKDYGTVDGTFYAAPLGANMKSFVWYNPGIFTEKGYAIPTTWDEMLALTDKIAADYPDSKPWCAGIESGGATGWPATDWVEDVMLRTAGPDVYDKWVSHEIPFNDPQVVAALDAVGAILKDPARVNGGFGDVKSIATTPWTDGGLPIIPEEGAAPKCFLHRAANFYQNNWPKGTTVAEDGDVFAFYLPGKTADDKPVLGGGEFVAAFRDAPEVAAFQAFLASDTWANAKAKATEGGGWVSANSGLDVNNLATDFDKLAASVLGDKNSVIRFDASDLMPAEVGAGSFWKEMVKFFSEDKSSQAVADAIEKTWP
>NZ_CP049862.1|WP_166415126.1|121366_122302_+|sugar-ABC-transporter-permease
MIVAVLLFVGVMALLLWLVDRPRRTRNWLVAGAFAGPALLLVGFGLVYPALSTTKGSFYDKRGQNFIGLDNYVRAFTDPDFQVVLRNTIIWVVLVPLLSTLIGLVYAVLVDRTRFEKAAKSLVFLPMAISMVGASVIWKFVYEYREASANQIGLLNQVLVWVGLEPQQFLLNQPLNTLFLIIVMVWIQAGFAMTILSASIKAIPDDIVEAARLDGLYGFGMFRYITVPSIRPALVVVLTTIAMATLKVFDIVRTMTAGNFGTSVVANEFYMQSFKFNDKGMGAALAVLLFIFVIPLIVYNVRQMRKVEEIR
>NZ_CP049862.1|WP_166412602.1|122298_123273_+|carbohydrate-ABC-transporter-permease
MTADSFPTTGDEVTQSAVPEADGATAPTTLTAATDSTVTRRARRLRKGFQSPWASLAAILIAFLWTIPTVGLLVTSFRPEKDIKRDGWWNVFTSPNFTLDNYDQALFGGGNDMATYLVNSVVISLPSVIIPISIALLAAYAFAWIPFRGRDVLFVAIFALQIVPIQVTLIPLLTQYVSWGIGRSFWPVWLSHTMFALPLAIFLLHNFMKEIPASLVEAARVDGAGHVKIFFRVLLPLLVPAIASFGIFQFLWVWNDLLVSLTFSGGRAAVAPLTVRLAEMVGTRGSDWFLLSAGAFIAMIVPVIVFLSLQRYFVRGLLAGSVKG
>NZ_CP049862.1|WP_166415127.1|123454_124468_-|NAD(P)H-quinone-oxidoreductase
MIAIDPGDGTAPARLADATAPVPDVRAGDVRVRVGAAGVNPADALQVRGLYPRPPGAPEWPGLEVAGTVVEVGGGVVGLRTGDRVAALLPGGGYAEEVVVPAGHALIVPAGLDDAHAAALPEGLCTAWSSLVDVGRLTPGSTVLVHGGAGGVGSLAAQLALVLGCRVVTTARGTARVAAVRELLSPALAHARAHGAGDDALTVLDRETDDFVEAATALGGADVTLDVVGAANLGRNVGALARDGRLVVIGLLKGRRGELDLGELLARRGTVVGTTLRSRTDDEKTAIVDDVREHVWPLVATGAVRSRVHARVPFERAAEALEMLASGEVVGKVVLVP

Crispr_ID: NZ_CP049862_5

• CRISPR_ID: NZ_CP049862_5
• CRISPR_location: 305010-305115
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP049862_5

Consensus_repeat	Method
CCGTCCGGCGCGTCGTCACCCGCGG	CRISPRCasFinder

spacers of NZ_CP049862_5

>5.1|305035|56|NZ_CP049862|CRISPRCasFinder
GCTCGGCGGGCTCCTCCGGGACGTCACCGTCGAGGAGGTGCGGGCCGACCACGATG

CRISPR arrays and Neighbor proteins around NZ_CP049862_5

CRISPR arrays

The CRISPR arrays of NZ_CP049862_5

>merge|NZ_CP049862|5|305010-305115|CRISPRCasFinder
CCGTCCGGCGCGTCGTCACCCGCGGGCTCGGCGGGCTCCTCCGGGACGTCACCGTCGAGGAGGTGCGGGCCGACCACGATGCCGTCCGGCACGTCGTCACCCGCGG

>NZ_CP049862|5|5|305010-305115|CRISPRCasFinder
CCGTCCGGCGCGTCGTCACCCGCGG	GCTCGGCGGGCTCCTCCGGGACGTCACCGTCGAGGAGGTGCGGGCCGACCACGATG
CCGTCCGGCACGTCGTCACCCGCGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP049862.1|WP_166412728.1|303288_303705_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412725.1|302132_302402_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412735.1|306708_307410_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412737.1|308474_309893_-|phage-portal-protein	unknown	unknown	gnl|CDD|377466
NZ_CP049862.1|WP_166412731.1|304478_304883_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412739.1|311567_312107_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412729.1|303704_304100_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412741.1|313485_314199_-|hypothetical-protein	unknown	unknown	gnl|CDD|366672
NZ_CP049862.1|WP_166412724.1|301391_302117_-|hypothetical-protein	unknown	unknown	gnl|CDD|276834
NZ_CP049862.1|WP_166412727.1|303030_303219_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412736.1|307467_308478_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412723.1|301071_301311_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412726.1|302512_303034_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412738.1|309906_311568_-|large-terminase	unknown	unknown	gnl|CDD|281364
NZ_CP049862.1|WP_166412733.1|305257_306277_-|major-capsid-protein-E	unknown	unknown	gnl|CDD|377147
NZ_CP049862.1|WP_166412730.1|304096_304486_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412734.1|306288_306675_-|potassium-transporter	unknown	unknown	unknown
NZ_CP049862.1|WP_166412740.1|312699_313026_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412742.1|314393_314786_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412722.1|300784_301075_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP049862.1|WP_166412737.1|308474_309893_-|phage-portal-protein	gnl|CDD|377466	pfam05133, Phage_prot_Gp6, Phage portal protein, SPP1 Gp6-like. This protein forms a hole, or portal, that enables DNA passage during packaging and ejection. It also forms the junction between the phage head (capsid) and the tail proteins. During SPP1 morphogenesis, Gp6 participates in the procapsid assembly reaction. This family also includes the old Pfam family Phage_min_cap (PF05126).	1.761e-13
NZ_CP049862.1|WP_166412733.1|305257_306277_-|major-capsid-protein-E	gnl|CDD|377147	pfam03864, Phage_cap_E, Phage major capsid protein E. Major capsid protein E is involved with the stabilisation of the condensed form of the DNA molecule in phage heads.	7.03552e-15
NZ_CP049862.1|WP_166412724.1|301391_302117_-|hypothetical-protein	gnl|CDD|276834	cd01383, MYSc_Myo8, class VIII myosin, motor domain. These plant-specific type VIII myosins has been associated with endocytosis, cytokinesis, cell-to-cell coupling and gating at plasmodesmata. The catalytic (head) domain has ATPase activity and belongs to the larger group of P-loop NTPases. It also contains IQ domains Myosins are actin-dependent molecular motors that play important roles in muscle contraction, cell motility, and organelle transport. The head domain is a molecular motor, which utilizes ATP hydrolysis to generate directed movement toward the plus end along actin filaments. A cyclical interaction between myosin and actin provides the driving force. Rates of ATP hydrolysis and consequently the speed of movement along actin filaments vary widely, from about 0.04 micrometer per second for myosin I to 4.5 micrometer per second for myosin II in skeletal muscle. Myosin II moves in discrete steps about 5-10 nm long and generates 1-5 piconewtons of force. Upon ATP binding, the myosin head dissociates from an actin filament. ATP hydrolysis causes the head to pivot and associate with a new actin subunit. The release of Pi causes the head to pivot and move the filament (power stroke). Release of ADP completes the cycle. CyMoBase classifications were used to confirm and identify the myosins in this hierarchy. .	0.00798255
NZ_CP049862.1|WP_166412738.1|309906_311568_-|large-terminase	gnl|CDD|281364	pfam03354, Terminase_1, Phage Terminase. The majority of the members of this family are bacteriophage proteins, several of which are thought to be terminase large subunit proteins. There are also a number of bacterial proteins of unknown function.	0.00143569
NZ_CP049862.1|WP_166412741.1|313485_314199_-|hypothetical-protein	gnl|CDD|366672	pfam01485, IBR, IBR domain, a half RING-finger domain. The IBR (In Between Ring fingers) domain is often found to occur between pairs of ring fingers (pfam00097). This domain has also been called the C6HC domain and DRIL (for double RING finger linked) domain. Proteins that contain two Ring fingers and an IBR domain (these proteins are also termed RBR family proteins) are thought to exist in all eukaryotic organisms. RBR family members play roles in protein quality control and can indirectly regulate transcription. Evidence suggests that RBR proteins are often parts of cullin-containing ubiquitin ligase complexes. The ubiquitin ligase Parkin is an RBR family protein whose mutations are involved in forms of familial Parkinson's disease.	0.00124079

Protein sequences

>NZ_CP049862.1|WP_166412731.1|304478_304883_-|hypothetical-protein
MSTLGVTPSDIRDAGFGLAIPGGTTVDAQIQKLIDKAEERLLAAVPSIPRRIAAGTLPAALAKGVVEDMVLRVIKNPRALRQMGVDDFQATIDTAVSSGALYVTGDERALLAPPLRGAVGSVRIGLPGWRLPGA
>NZ_CP049862.1|WP_166412730.1|304096_304486_-|hypothetical-protein
MRDVMLYARQVGATLAESLFIDSARVERAGAKDPLTGLPVLSLVYRGECKVQESRVPTGTELEAGGHEYVVHTRQVHFPVAAFTPEPGMLVTVESAGVDETLVGRTFRVSRRPGKTTATAMRLTVEDPS
>NZ_CP049862.1|WP_166412729.1|303704_304100_-|hypothetical-protein
MTSLESSGFAEAIEAFAAAESAVESQARAVVERGAVNIKKQLQRELSGSKHFKGIARDVSYDIRTAGAFGGGVIEAEIGPESVPGSAGNLANVAYFGTSRGGGTVPDPSLALAAEVPKFERELARLVGEGL
>NZ_CP049862.1|WP_166412728.1|303288_303705_-|hypothetical-protein
MLAHIESIKAALVPLGWQVHYVNVPEPPTFPYVLLWSGTGDPGSEPPLCGPMDDLEAVVGVTVVAGSPEGVLMVQSAVRAVLSPGDARTRLTVAGRAASLKRTGGQTVQVDRDVKIPGTNTSPAFSVDLYDLHSTPAT
>NZ_CP049862.1|WP_166412727.1|303030_303219_-|hypothetical-protein
MAFVEVYRKDTGEKVRVPESHLRIFPESFTRTPRRPAEVKAAPAASTTKPADKPAVNPKEDA
>NZ_CP049862.1|WP_166412726.1|302512_303034_-|hypothetical-protein
MSVKTLADGNVKVTLLAAKPADKNAIVLTALTDVGAKDISCNILSNDFDYGPTGSETVDEKPLCAEGNGQTPGLSNYSGGMTVFRYWDPATGLADSTDDFLWEAVKEKGTTLYLAVRDSHKKSKEAWTAGDEYRYFEVVTDDPQRGDRAGFIKYRVTLLHQDAALDKLVVAGP
>NZ_CP049862.1|WP_166412725.1|302132_302402_-|hypothetical-protein
MSITIPGVPEFLTREQYLALLRAIGFEPDDIREIRYAHDGVHALLFARDEHGRKRIDPSTSSYYKHRVFIPIRDEDGDERTTRITPAKN
>NZ_CP049862.1|WP_166412724.1|301391_302117_-|hypothetical-protein
MTDINVSAESAQTIDLEAWLGGATVAEASVEVYQRPDLLARIEEWQRRYERAEQSDIGERSAGEEDPLAALEAEGEALVAELEASKSVWFLRALSSADEKAIDEAHPFPERPEVFAEKPPFMQARPTEAQARAFSQAYEAWGVRKKMFDAEHAAETDAYVQGATAALIARGVEKIVRALSRIEVGGEVIASSITLEQAQGLPARLGEVQVGKIITAIDTATNLEPAVPAGFGRRGSGTTQD
>NZ_CP049862.1|WP_166412723.1|301071_301311_-|hypothetical-protein
MALALSIYEDGMTADGLPASVVYGDERGTWLEAKPRINYAEAARQQWHKDNPNPEPGTVLEIVDTWPGEPAEGDDNEAG
>NZ_CP049862.1|WP_166412722.1|300784_301075_+|hypothetical-protein
MGFLIAVVVGFLLFAGVIGYFSFAEGERARDKAEKNADTFFAETFDGRPDVIVTINMRTPSYETVVLGAMDRGYRLVHESTVVESLDVKRLIFERG
>NZ_CP049862.1|WP_166412733.1|305257_306277_-|major-capsid-protein-E
MALWTDIITPAELTGYIREDLSAVEQRRGSLARFLPNRVVPDIVVRFIAGQAGLVPEAEFRAYDAEPTVGKRPSGKRTVLELPAIGQNIPVSEYDQLRTRNASDDVLLEQILSTARRVVLAVADRMERLRGVVLSTGVATIPEIGAADAFGRSASHTVTASALWDSATSVSRLADLQTWSDAYEATNGVAPGAILMSRKALRVLAQGDEFKTSLVGGGSRPATVADVNSIIEGAGLPPVEVYTRRSASGLILPEKEVLLLPAPVEPDAWEDTQLGASFWGQTLSSSEAGWGIEESEQPGIVAGVYRNEKPPMIAEVVSDAIGMPVLANADLSFKATVLA
>NZ_CP049862.1|WP_166412734.1|306288_306675_-|potassium-transporter
MPRLTTETFGGGDQSWLGSTHGIANARTEVLDISAFTAGTHYPNGYIPSGTPVAKVGGVLVPYDKTEATTTAAGVLAGFILTDQRVVGTADFAVPLLDHGRVRASKVPNSFVAPVAAEKRAATTIVYV
>NZ_CP049862.1|WP_166412735.1|306708_307410_-|hypothetical-protein
MSKSLYRPATDSIDPTAPGGVEAMLAFHRLTFGDARMEAEGDGGEGEGEAAASFKDPDTGDTYAFPPNTPVKDMTEGQKSEYWRHKARKHEDRVKTMSDYETLKAERDALKSKHLTDDEKALDAATTSAAEKARAEVRSEYAARLVTAEFRAANSGRIPADKLTAVLDGIEPTKFLTADGEVDTDKVQTFVDGIAPAKSEKWPDMGQGRRSQGDSKSVAAGRDLYSSRHAKKS
>NZ_CP049862.1|WP_166412736.1|307467_308478_-|hypothetical-protein
MSVARARSLVDMETAAQAKVEREAVARAVAAVGAVESWYMPADVQALSRQIGATARSASRAAAGTTDAYLTRMLSMMLDAPAKSVGVLDLSTPLRAGVESYEQVYARVAEHVRYLESTGMSRWEAVERAQTRVDAMVRTDLALARRGQSRAVYAGTPRVTGYRRIIRPELSTTGTCGLCAAASGRVYSRDTLLPIHYRCKCTTMPILGENDPGREIDDETLAQIYDAAGSTGAADLKQVRFTVVQHAELGPTLVDPKHRSTHPGTRPSAAPRSARGPQRPSMPVDPARMLAAEIRALESRLPMLEARAATGEPGLDQAIAYQRERIALLGTRLRAL
>NZ_CP049862.1|WP_166412737.1|308474_309893_-|phage-portal-protein
MSIDVKTVQSPGWWLQRLSRKMDDRQKMVSDLFARYEGDAPVPSSLRDAPESAKRFFKAARTAFAEMIVKSVKYPLRLQGVATGVDTGEGGDPAAWRMVVRSGMRTEGDDAIRLALTAGNGYAIVGMHGDEPRYTSEDPRQVVTIHDPVVQSEVLAAAKFFHHDVDERAYAYLYRPGRVWRAFTDRKRPNGARFASSWKWDPEFGGEEGQALPEGCEKLVPVFRYRNEEGVGEFQRHRDLLDRLDHMVLQGMSIATYQAFRQRALKIDPKDMPAEDPETGAEIDYNDVFSADPGSLWTLPPTADLWESGNVDLTPVWTGMEKFTQQLSAVTFTPLAMFSPEGQNQSAAGSAFAREGRTFKIEDRQDRFGETHARALAALFLMTGDTERSRFEDLDIIWRPAERYSLAEKADAAVKAKASNVPWHTIMRDVWQYSPEQIARMESERVDDLFLTGAAASTALPADDAAGDAVQP
>NZ_CP049862.1|WP_166412738.1|309906_311568_-|large-terminase
MGLLVVPGADAEPWPTIGGEVCDFIEERAVYGPGSLQGQPYVIDPEFRAFIYRLFEVYPQGHPWAGRRRFKRGGLSVRKGLAKTEKEALLVYAHIHPEGPGKCDGFDADGHPVAAPVMSPYVPMLAFSLDQVEELAYGALKYVIENGPDSDLFDVSLERALRLDDWGRSDGGAWPLANAPDSRDGGRTTLNAFDEPHRLHLPRHIKAHETMAANLAKRPLEDPWSLYVGTAGELGQGSVAENLHAEAEAIRDGKIERPDLFYLYRTDDGGHDLEVKAERTKAVAEATGPAGEWGPGQFDDIASQWDRPGVDKAYLERVWLNRWVKSGQQAFDVKRWSDLKHEGGDVDKPLRGRIPAGAPVAVGFDGARRRDSTAFVITDLLTGTQEIAGLWEKDLDDDEWEVPEAEVDQTVEHIFSRYNVWRLYGDPPYWVTEMGVWAGRHKGLVEEWWTNHYKKAAYAIRAYQEAIASGAVGWTASDPHAPELARHIAAAGQVKLKNIVDDEGKPLYILGKIHPDRKFDAAMAAMLSWQAYLDGVKAGQAKPHVPARPRRIR
>NZ_CP049862.1|WP_166412739.1|311567_312107_-|hypothetical-protein
MPADGREGAAVPPWPLQPDVEKQAAFELARDRVAALQVEVEEAEDGRTKGRLRRDLNKNEMLVATLGLQIEQARDAEVALWADLWAMPQAAIWEESHSGREVAQYVRWKIRAEQGDLKAATEARMLSDRLGLNPKALMSLRAEIERAEEAEDRGERRRETRKPKPKSGEDPRGGLYAVG
>NZ_CP049862.1|WP_166412740.1|312699_313026_+|hypothetical-protein
MTNPLAEKAPAAAATIRNVSDALNDGRDPGVAMAASTQAELDAITERFENAALAHSREGMIAAWNELVHFMTAYSGALASIGVFLLASVRNMSEFSTDEILGSALEQF
>NZ_CP049862.1|WP_166412741.1|313485_314199_-|hypothetical-protein
MTDAKTALEASRNLAWIANHWPDLEAALTPGGGNALTGMPRTDSTGIPINIHVSDLMREIDDHARHLCLQLIDETHDITDMPPTPAARLHLAAQRYGHWCAADPTTAHTYTDTAHDYREKTRRVLEKPLAPTYLGPCPTPDCDGELYQRGATTRLTCPACHHETDVTTQRAYLAEQMEERLMTLSEITSALVVAGHPVPHSTVRRWASSRRLRHITDGLYKFTDALTLAEHRAARTA
>NZ_CP049862.1|WP_166412742.1|314393_314786_-|hypothetical-protein
MTDRPRMPESMASRNLAHLDALTLAVCHLRDRTYSRRRFLDEAARLADWYNIDHINERRAAAKATADTADRPRLASPEHAATYPLRLVVIRDLNAEGWPEWTVCLGTQDISTHATHAEAITAADKLARQH

Crispr_ID: NZ_CP049862_6

• CRISPR_ID: NZ_CP049862_6
• CRISPR_location: 333988-334095
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP049862_6

Consensus_repeat	Method
CTCGTGGGACGTCGTGCCCGTCGG	CRISPRCasFinder

spacers of NZ_CP049862_6

>6.1|334012|60|NZ_CP049862|CRISPRCasFinder
TACCTGGACGCGCGACGAGCCCGCAGCGCCCGCGCCCGTGAACCCTGCGCCCACGGACGT

CRISPR arrays and Neighbor proteins around NZ_CP049862_6

CRISPR arrays

The CRISPR arrays of NZ_CP049862_6

>merge|NZ_CP049862|6|333988-334095|CRISPRCasFinder
CTCGTGGGACGTCGTGCCCGTCGGTACCTGGACGCGCGACGAGCCCGCAGCGCCCGCGCCCGTGAACCCTGCGCCCACGGACGTCACGTGGGACGTCGTGCCCGTCGG

>NZ_CP049862|6|6|333988-334095|CRISPRCasFinder
CTCGTGGGACGTCGTGCCCGTCGG	TACCTGGACGCGCGACGAGCCCGCAGCGCCCGCGCCCGTGAACCCTGCGCCCACGGACGT
CACGTGGGACGTCGTGCCCGTCGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP049862.1|WP_166412777.1|340211_340907_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225107
NZ_CP049862.1|WP_166412778.1|341155_342094_+|hypothetical-protein	unknown	unknown	gnl|CDD|226951
NZ_CP049862.1|WP_166412779.1|342102_343143_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412775.1|338396_339473_+|aspartate-semialdehyde-dehydrogenase	unknown	unknown	gnl|CDD|237845
NZ_CP049862.1|WP_166412765.1|326651_327053_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|238045
NZ_CP049862.1|WP_166412773.1|336680_336866_+|antitoxin	unknown	unknown	gnl|CDD|379416
NZ_CP049862.1|WP_166412774.1|337110_338394_+|aspartate-kinase	unknown	unknown	gnl|CDD|235843
NZ_CP049862.1|WP_166412763.1|326064_326298_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|378935
NZ_CP049862.1|WP_166412766.1|327049_327448_+|ImmA/IrrE-family-metallo-endopeptidase	unknown	unknown	gnl|CDD|368753
NZ_CP049862.1|WP_166415143.1|335179_335752_+|DUF5063-domain-containing-protein	unknown	unknown	gnl|CDD|374737
NZ_CP049862.1|WP_166412771.1|334569_335169_+|recombination-protein-RecR	unknown	unknown	gnl|CDD|234616
NZ_CP049862.1|WP_166412761.1|325450_325612_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412768.1|329454_330552_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|236863
NZ_CP049862.1|WP_166412764.1|326300_326555_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|238045
NZ_CP049862.1|WP_166412772.1|335748_336534_+|TSUP-family-transporter	unknown	unknown	gnl|CDD|182593
NZ_CP049862.1|WP_166412769.1|330548_331232_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|224922
NZ_CP049862.1|WP_166412762.1|325724_325967_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412776.1|339569_339974_-|SHOCT-domain-containing-protein	unknown	unknown	gnl|CDD|378276
NZ_CP049862.1|WP_166412767.1|328417_329317_+|methionine-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|224381
NZ_CP049862.1|WP_166412760.1|324531_325287_-|hypothetical-protein	unknown	unknown	gnl|CDD|226144

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP049862.1|WP_166412777.1|340211_340907_+|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].	2.68891e-24
NZ_CP049862.1|WP_166412778.1|341155_342094_+|hypothetical-protein	gnl|CDD|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	3.84209e-12
NZ_CP049862.1|WP_166412775.1|338396_339473_+|aspartate-semialdehyde-dehydrogenase	gnl|CDD|237845	PRK14874, PRK14874, aspartate-semialdehyde dehydrogenase; Provisional.	0
NZ_CP049862.1|WP_166415143.1|335179_335752_+|DUF5063-domain-containing-protein	gnl|CDD|374737	pfam16702, DUF5063, Domain of unknown function (DUF5063).	7.09244e-33
NZ_CP049862.1|WP_166412773.1|336680_336866_+|antitoxin	gnl|CDD|379416	pfam14013, MT0933_antitox, MT0933-like antitoxin protein. This family of proteins contains the MT0933 protein, which has been identified as an antitoxin to /protein MT0934. This family of proteins is found in bacteria. Proteins in this family are typically between 61 and 90 amino acids in length.	8.57631e-06
NZ_CP049862.1|WP_166412774.1|337110_338394_+|aspartate-kinase	gnl|CDD|235843	PRK06635, PRK06635, aspartate kinase; Reviewed.	0
NZ_CP049862.1|WP_166412763.1|326064_326298_-|helix-turn-helix-domain-containing-protein	gnl|CDD|378935	pfam12728, HTH_17, Helix-turn-helix domain. This domain is a DNA-binding helix-turn-helix domain.	1.12684e-05
NZ_CP049862.1|WP_166412766.1|327049_327448_+|ImmA/IrrE-family-metallo-endopeptidase	gnl|CDD|368753	pfam06114, Peptidase_M78, IrrE N-terminal-like domain. This entry includes the catalytic domain of the protein ImmA, which is a metallopeptidase containing an HEXXH zinc-binding motif from peptidase family M78. ImmA is encoded on a conjugative transposon. Conjugating bacteria are able to transfer conjugative transposons that can, for example, confer resistance to antibiotics. The transposon is integrated into the chromosome, but during conjugation excises itself and then moves to the recipient bacterium and re-integrate into its chromosome. Typically a conjugative tranposon encodes only the proteins required for this activity and the proteins that regulate it. During exponential growth, the ICEBs1 transposon of Bacillus subtilis is inactivated by the immunity repressor protein ImmR, which is encoded by the transposon and represses the genes for excision and transfer. Cleavage of ImmR relaxes repression and allows transfer of the transposon. ImmA has been shown to be essential for the cleavage of ImmR. This domain is also found in in metalloprotease IrrE, a central regulator of DNA damage repair in Deinococcaceae, HTH-type transcriptional regulators RamB and PrpC.	1.95024e-10
NZ_CP049862.1|WP_166412771.1|334569_335169_+|recombination-protein-RecR	gnl|CDD|234616	PRK00076, recR, recombination protein RecR; Reviewed.	7.9886e-120
NZ_CP049862.1|WP_166412765.1|326651_327053_+|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.	9.9175e-07
NZ_CP049862.1|WP_166412768.1|329454_330552_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|236863	PRK11153, metN, DL-methionine transporter ATP-binding subunit; Provisional.	1.04278e-158
NZ_CP049862.1|WP_166412764.1|326300_326555_-|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.	0.000195079
NZ_CP049862.1|WP_166412772.1|335748_336534_+|TSUP-family-transporter	gnl|CDD|182593	PRK10621, PRK10621, hypothetical protein; Provisional.	1.20221e-39
NZ_CP049862.1|WP_166412769.1|330548_331232_+|ABC-transporter-permease	gnl|CDD|224922	COG2011, AbcD, ABC-type metal ion transport system, permease component [Inorganic ion transport and metabolism].	2.52402e-84
NZ_CP049862.1|WP_166412776.1|339569_339974_-|SHOCT-domain-containing-protein	gnl|CDD|378276	pfam09851, SHOCT, Short C-terminal domain.	0.00156118
NZ_CP049862.1|WP_166412767.1|328417_329317_+|methionine-ABC-transporter-substrate-binding-protein	gnl|CDD|224381	COG1464, NlpA, ABC-type metal ion transport system, periplasmic component/surface antigen [Inorganic ion transport and metabolism].	7.357e-79
NZ_CP049862.1|WP_166412760.1|324531_325287_-|hypothetical-protein	gnl|CDD|226144	COG3617, COG3617, Prophage antirepressor [Transcription].	3.10184e-37

Protein sequences

>NZ_CP049862.1|WP_166412769.1|330548_331232_+|ABC-transporter-permease
MNLVAAARPTDWDKMLPALWRSLGETLYMVSVSLLVALVAGLALGLALYVTRAGNLYGNRAVNIVLNVVVNIVRPIPFIIFLTAIGPLTLSVVGTTVGTEAVILPMSIMASFAFSRLVEQNLVAVDPGVVEAARAMGASRFRVVWSVLVPEALGPLILGYTFLFIGVVDMSAMAGMIGGGGLGDFAIRFGYQRFNWEVTFVAVLVIVVLVQIAQGVGNLLARKVLRR
>NZ_CP049862.1|WP_166412768.1|329454_330552_+|ATP-binding-cassette-domain-containing-protein
MSEREPKIVFEAATKVFRTTKGEVRAVDGVNLTIRAGEVYGVIGYSGAGKSTLVRLINALEPVTSGRVLVDGRDVHSLKESALRAARADIGMIFQQFNLLSSRTVAGNVAYPLKVAGWPRAKRDARVAELLDFVGLTDKARAFPSQLSGGQKQRVGIARALATNPTILLADESTSALDPETTQDVLDIVKRVNVELGVTVVVITHEMEVVKYVCDRVAVMEGGKVVEHGDVYDVFARPQHAATRRFVGTALRDRPSPAALERLRRRHPGRIVTVGVREDGGATGELTRALRDHPVDGTVIYGGITEIAERPYGSLTLEIAGDDVAIAAFLTDLGRSTTVLDLGTAAHPLSDPDAVGPRASKGASA
>NZ_CP049862.1|WP_166412767.1|328417_329317_+|methionine-ABC-transporter-substrate-binding-protein
MNRKLTAIAAATALLLGLAACASDETPAASGTTGGSAAPKAVRIGVVGSQDDQWPIFAEKAKAAGIDVEIVNFSDYALPNPALSQGQIELNQFQHIQYLADYNVNADDDLVAIGATAIYPLALYSKKHTALTDIPDGAEIAVPNDQTNLNRALFVLQAAGLIKLDGGGTLTSTELDVLPESKVKVTPVSAEQTAVSLESLDGAVVNNDFVLDAGLDPKAALAQDDPASPAAQPYINIWTARAADKDNATYLKLVKIFQDTAVTDALQEQSKGTAVLRADDAAALATILKTTEDNIRAGK
>NZ_CP049862.1|WP_166412766.1|327049_327448_+|ImmA/IrrE-family-metallo-endopeptidase
MTLDELVAHAEEQGLRVVWRDLGRRSGELTRAGLVVVNHRKSTLTQRITIAHEVGHHWHGHDWTRAHDVERDERQADLYAARLLIDPHAMERAAAVVGCHPGAIARELGVTTHLVTLWLEQPQPSTRCGLIA
>NZ_CP049862.1|WP_166412765.1|326651_327053_+|helix-turn-helix-transcriptional-regulator
MNIRSEEFPAYVGLELKGKIVSRGFTALDVATRIGRSPAAFNRWLNGKVDIPLAVLCAAAEVIDVDPQEIVGHAYDRLVVRHGERTGFIYDADEIEHAKSANDALRAMSPADVMLAARDVDDDAEAEAQTEDA
>NZ_CP049862.1|WP_166412764.1|326300_326555_-|helix-turn-helix-transcriptional-regulator
MNNHAASTTIEWSARAVREAIADTGRSKVSISDETGIPYATLNRKLAAKGEFSFRELLLIAEALGVSPSTFTPPAFARVERTAA
>NZ_CP049862.1|WP_166412763.1|326064_326298_-|helix-turn-helix-domain-containing-protein
MTAETFDATEAGRRLGLTARTVLDMARRRDIGHVKVGRRVRFTEAIVAEYIATRTVGVGLARTARSQAAHRRRKPAA
>NZ_CP049862.1|WP_166412762.1|325724_325967_-|hypothetical-protein
MPTLTAYENRIATYAAENNHSVSRGQVKRIARDLYERQARMSDVDLERVFMVADPTPPTAFREIARNDRAAARRLGLVPA
>NZ_CP049862.1|WP_166412761.1|325450_325612_-|hypothetical-protein
MNSCKCGSPVELGNPDLGIFQCERCWEAWSRWADAHRDQPLDAWPGIAEAAAA
>NZ_CP049862.1|WP_166412760.1|324531_325287_-|hypothetical-protein
MTSNIVPFEFDGAQVRVVTIDGDPWFVGTDVTRILGYANPSDALQRIDDDDLRFATLALSEGSREVSRLRPLVNESGVYALAFGSTLPRAVDFRRWVTREVLPSIRRTGSYGTPALTGPALMAAALIEAQAVLEAREAQVAELTPRAEAWDALAATDGDYSMRDAAQILCRDHGIDIGQNRLSKRLREIGWVDPAGIPYQRHVDLGRLRSRARYYTHARTQERVLADPQIRVTPKGIADLRTILATKENVA
>NZ_CP049862.1|WP_166412771.1|334569_335169_+|recombination-protein-RecR
MYEGAVQDLIDELGRLPGVGPKSAQRIAFHLLAADADDVRRLVDALTQVKARVKFCEVCGNVAEEERCRVCRDPRRSPSVICVVEEPKDVVAIERTREFRGTYHVLGGAINPIDNVGPDDLRISQLMSRLADGQVTEVILATDPNVEGEATATYLARLLGPMGLRVTRLASGLPVGGDLEYADEVTLGRAFEGRRVVHG
>NZ_CP049862.1|WP_166415143.1|335179_335752_+|DUF5063-domain-containing-protein
MTLPGGVTEVGAAFAEQASNFVATVTHVASGATPEAAIPVLLLATTDVLASGSRLGAMVDVVPAEEFEPDSGPDTDVEPLRVALALILDGLDSYPEVVDPVLGAELDTTSLSDGLAEITLALTQGLAHHEAGHPAEALWWWQFSYLSGWGATAASAARVLASILGHLRLDVDDDVAAEAEYDALQRHTTG
>NZ_CP049862.1|WP_166412772.1|335748_336534_+|TSUP-family-transporter
MTTGGLDLSTTTVLLLVVAGFAAGWIDAVVGGGGLVQLPALLLVPGISPVQALATNKLAGIMGTSVAAVTFYRRVGPDLRTAAPMAVCAFGGAVGGAALASRIPAELFTPIILVVLIGVAAWTIARPSLGSSSALRWEGNRHVLTAAAVGLAIGAYDGLLGPGTGTFLVISLVGLLGYAFLPASAIAKIVNFATNAGALVFFVPHGAVLWGLGLVVGAANLCGGYLGARMAVAKGSGFVRGAFIVVVSVLVVRLGWQVLAG
>NZ_CP049862.1|WP_166412773.1|336680_336866_+|antitoxin
MGIDDLAAKAKDALAEHGDKVSDGLEKAAEFVKSKTSDDVDAKIDSAVDAAQGFIAKQQQA
>NZ_CP049862.1|WP_166412774.1|337110_338394_+|aspartate-kinase
MALIVQKYGGSSVSDAESIKRVAKRIAESKRAGNDVVVVVSAMGDMTDELIDLAQQVTPAPPQREMDILLTAGERISMSLLAMAINNLGVKAKSFTGQQAGVITDAVHGKAHIVDVVPSRVRETIEKGSVAIVAGFQGVTRDTNDVTTLGRGGSDTTAVALAAGLGADVCEIYSDVDGVFTADPRIVPAARKVDRLTYEEMLEMAASGAKILHLRCVEYGRRYDVPIHVRSSFSGKEGTLVTNRPLTAENGEELPMEEPIITGVAHDRSEAKITVVGVPDVPGTAARIFEVVATAGANIDMIVQNISAAQTGLTDISFSLPEGDVPATLAALRVAQEEIKFESLQFDDQIGKLSLVGAGMKSSPGVSAKLFGALRDAGINIEMISTSEIRISVVTREDSLDDAVRAVHTAFGLDGEAEAVVYAGTGR
>NZ_CP049862.1|WP_166412775.1|338396_339473_+|aspartate-semialdehyde-dehydrogenase
MTENLTVAVVGATGQVGGVMRRLLVERDFPVGTIRYFASARSAGKVLDWKGTDVVVEDVATADLEGIDIAIFSAGGSTSKEHAPRFAAAGAVVIDNSSAWRLDVDVPLVVSEVNPDAVTEARKGIIANPNCTTMAAMPVLKPLSDAAGGLQRLIVSTYQAVSGSGLAGATELADQVRAAVAGDVALEELVTDGSAVTLPEPSKYVRNIAFNVVAIAGGIVDDGSLETDEEQKLRNESRKILGLPDLAVSGTCVRVPVFSGHSLVVNAEFGEPISPEQATALLEQAPGVEVTDVPNPLQAAGADPSFVGRIRVDQSVPGGKGLALFISNDNLRKGAALNAVQVAEVVAPRLAEVRAARV
>NZ_CP049862.1|WP_166412776.1|339569_339974_-|SHOCT-domain-containing-protein
MNIPSFWSTIGTTIWWFLAVFLLISYLMVIFSIIGDVFRDRELGGLAKAIWVFFLVTTPVLTALVYLVVRGRGMGERAVVHASEARTSTEEYIRSVAGGGAIDEISRAKNLLDAGAITADEYATLKAVALRTTS
>NZ_CP049862.1|WP_166412777.1|340211_340907_+|response-regulator-transcription-factor
MPPTRHNGAQTNDIEEVAVVARARIGVVDDHPSVILGVSAILNVSADLVVSAWGPTVDSVLVQDEGLDLVLLDLVLGDGSTPTLNVAQLRAAGVPVLAFTSGDRPSTIREAGRAGAVGMVRKSETPTAVLAAVRGALRGEVVATSDWAAALDHDTDFVTARLSDREAEVLALYASGETAERVARTLFISRQTVLDHLRRIRAKYAAVDRTAPTKIDLFHRAVEDGLVPPGG
>NZ_CP049862.1|WP_166412778.1|341155_342094_+|hypothetical-protein
MGIPILSAVLNAATFVAFEGPDADAAVPWVWALEPIAVSLLALRVPVVWAVSAALGAALLPTASGLLVLGHVPEAVLVLTPWHLANVAFVVIFAGIRVRLRAFGESEEAARRGAEEHARAESEVRRLAALGLLVHDEVLTVLAVAATTGRDGGDAVSDALRVEARHGLGLLGGAPAGRTAVAGSSGQVAASLSASLRRIDPTIVLDVETLDASPPPPDVVDVLARAAAEAVRNSLRHAGEGVTRRVAVRVGGLSVGVVVRDDGCGFTDLEGRDGRLGVREGILARVRAMPGGTAELRSAPGAGTTVLLGWSA
>NZ_CP049862.1|WP_166412779.1|342102_343143_+|hypothetical-protein
MDAATVAAGSAGAGMGITSTRWVLCAVWGLGILTAVIDARLGRPSVASPLAFATLLGGVWAISTPGTDVLGRGRALLVIAGALATVTVVATTGPAQGRTWLVDLSGYLLALLVARGNGRTGAAGFVAFSAILMVWVAQGGSQAPLGEVLGAPVLALAGGVVWHLVLRRAVTRERAHRSEAARAASDARIARRAVDADRLEIAAINDVVAPVLRRILDGGVPDAASRLDAAVAEATVRDRIRSPWEPGGALDLCVEDRRRAGIVVVQIGERTGPRAAMPSALADRLVAIVAPVRTGRVTVRTLPPGRGVAMTVVVDDGATVSRTAVSIDGTVVDESRHGYSGQMSGT

Crispr_ID: NZ_CP049862_7

• CRISPR_ID: NZ_CP049862_7
• CRISPR_location: 521915-522010
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP049862_7

Consensus_repeat	Method
GCGACTCGTAGCGCTCCTGCACAC	CRISPRCasFinder

spacers of NZ_CP049862_7

>7.1|521939|48|NZ_CP049862|CRISPRCasFinder
AGCGCGAGCACCCGCCGGCCCTTCGCCGCCCCGTGCCGGCCAACATCC

CRISPR arrays and Neighbor proteins around NZ_CP049862_7

CRISPR arrays

The CRISPR arrays of NZ_CP049862_7

>merge|NZ_CP049862|7|521915-522010|CRISPRCasFinder
GCGACTCGTAGCGCTCCTGCACACAGCGCGAGCACCCGCCGGCCCTTCGCCGCCCCGTGCCGGCCAACATCCGCGACTCGTAGCGCTCCTGCACAC

>NZ_CP049862|7|7|521915-522010|CRISPRCasFinder
GCGACTCGTAGCGCTCCTGCACAC	AGCGCGAGCACCCGCCGGCCCTTCGCCGCCCCGTGCCGGCCAACATCC
GCGACTCGTAGCGCTCCTGCACAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP049862.1|WP_166412925.1|522138_523893_+|trypsin-like-serine-protease	unknown	unknown	gnl|CDD|273938
NZ_CP049862.1|WP_166412928.1|526765_528061_+|geranylgeranyl-reductase-family-protein	unknown	unknown	gnl|CDD|273936
NZ_CP049862.1|WP_166415159.1|511705_512539_-|aldo/keto-reductase	unknown	unknown	gnl|CDD|381357
NZ_CP049862.1|WP_166412930.1|528624_529176_+|NADH-quinone-oxidoreductase-subunit-B	unknown	unknown	gnl|CDD|235797
NZ_CP049862.1|WP_166412929.1|528233_528596_+|NADH-quinone-oxidoreductase-subunit-A	unknown	unknown	gnl|CDD|181171
NZ_CP049862.1|WP_166412923.1|519073_520039_+|o-succinylbenzoate-synthase	unknown	unknown	gnl|CDD|235084
NZ_CP049862.1|WP_166412922.1|517430_518933_+|PTS-fructose-transporter-subunit-IIBC	unknown	unknown	gnl|CDD|236740
NZ_CP049862.1|WP_166412921.1|516981_517434_+|PTS-sugar-transporter-subunit-IIA	unknown	unknown	gnl|CDD|334031
NZ_CP049862.1|WP_166412918.1|513838_514987_+|calcium:proton-antiporter	unknown	unknown	gnl|CDD|223464
NZ_CP049862.1|WP_166412927.1|525866_526568_+|demethylmenaquinone-methyltransferase	unknown	unknown	gnl|CDD|234689
NZ_CP049862.1|WP_166412924.1|520046_521873_+|2-succinyl-5-enolpyruvyl-6-hydroxy-3--cyclohexene-1-carboxylic-acid-synthase	unknown	unknown	gnl|CDD|236020
NZ_CP049862.1|WP_166412932.1|529897_531250_+|NADH-quinone-oxidoreductase-subunit-D	unknown	unknown	gnl|CDD|180385
NZ_CP049862.1|WP_166412919.1|515267_516029_+|DeoR/GlpR-transcriptional-regulator	unknown	unknown	gnl|CDD|224268
NZ_CP049862.1|WP_166412933.1|531246_532044_+|NADH-quinone-oxidoreductase-subunit-NuoE	unknown	unknown	gnl|CDD|181024
NZ_CP049862.1|WP_166412934.1|532040_533384_+|NADH-quinone-oxidoreductase-subunit-NuoF	unknown	unknown	gnl|CDD|131014
NZ_CP049862.1|WP_166412920.1|516025_516979_+|1-phosphofructokinase	unknown	unknown	gnl|CDD|238570
NZ_CP049862.1|WP_166412917.1|512711_513674_-|1,4-dihydroxy-2-naphthoyl-CoA-synthase	unknown	unknown	gnl|CDD|181386
NZ_CP049862.1|WP_166412916.1|511377_511602_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166412926.1|524491_525808_-|isochorismate-synthase	unknown	unknown	gnl|CDD|224091
NZ_CP049862.1|WP_166412931.1|529172_529901_+|NADH-quinone-oxidoreductase-subunit-C	unknown	unknown	gnl|CDD|181115

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP049862.1|WP_166412925.1|522138_523893_+|trypsin-like-serine-protease	gnl|CDD|273938	TIGR02037, Probable_periplasmic_serine_protease_do/HhoA-like, periplasmic serine protease, Do/DeqQ family. This family consists of a set proteins various designated DegP, heat shock protein HtrA, and protease DO. The ortholog in Pseudomonas aeruginosa is designated MucD and is found in an operon that controls mucoid phenotype. This family also includes the DegQ (HhoA) paralog in E. coli which can rescue a DegP mutant, but not the smaller DegS paralog, which cannot. Members of this family are located in the periplasm and have separable functions as both protease and chaperone. Members have a trypsin domain and two copies of a PDZ domain. This protein protects bacteria from thermal and other stresses and may be important for the survival of bacterial pathogens.// The chaperone function is dominant at low temperatures, whereas the proteolytic activity is turned on at elevated temperatures. [Protein fate, Protein folding and stabilization, Protein fate, Degradation of proteins, peptides, and glycopeptides].	1.04092e-90
NZ_CP049862.1|WP_166412928.1|526765_528061_+|geranylgeranyl-reductase-family-protein	gnl|CDD|273936	TIGR02032, Uncharacterized_protein_MJ1520, geranylgeranyl reductase family. This model represents a subfamily which includes geranylgeranyl reductases involved in chlorophyll and bacteriochlorophyll biosynthesis as well as other related enzymes which may also act on geranylgeranyl groups or related substrates. [Biosynthesis of cofactors, prosthetic groups, and carriers, Chlorophyll and bacteriochlorphyll].	2.89493e-77
NZ_CP049862.1|WP_166415159.1|511705_512539_-|aldo/keto-reductase	gnl|CDD|381357	cd19131, AKR_AKR5C2, Escherichia coli 2,5-diketo-D-gluconic acid reductase A (DkgA/YqhE) and similar proteins. Escherichia coli DkgA/YqhE is a founding member of aldo-keto reductase family 5 member C2 (AKR5C2). DkgA/YqhE (EC 1.1.1.274), also called 2,5-DKG reductase A, or 2,5-DKGR A, or 25DKGR-A, or AKR5C, catalyzes the reduction of 2,5-diketo-D-gluconic acid (25DKG) to 2-keto-L-gulonic acid (2KLG). It is also capable of stereoselective -keto ester reductions on ethyl acetoacetate and other 2-substituted derivatives.	3.82849e-131
NZ_CP049862.1|WP_166412930.1|528624_529176_+|NADH-quinone-oxidoreductase-subunit-B	gnl|CDD|235797	PRK06411, PRK06411, NADH-quinone oxidoreductase subunit NuoB.	7.91802e-101
NZ_CP049862.1|WP_166412929.1|528233_528596_+|NADH-quinone-oxidoreductase-subunit-A	gnl|CDD|181171	PRK07928, PRK07928, NADH dehydrogenase subunit A; Validated.	2.66621e-59
NZ_CP049862.1|WP_166412923.1|519073_520039_+|o-succinylbenzoate-synthase	gnl|CDD|235084	PRK02901, PRK02901, O-succinylbenzoate synthase; Provisional.	6.16207e-147
NZ_CP049862.1|WP_166412922.1|517430_518933_+|PTS-fructose-transporter-subunit-IIBC	gnl|CDD|236740	PRK10712, PRK10712, PTS system fructose-specific transporter subunits IIBC; Provisional.	1.43381e-114
NZ_CP049862.1|WP_166412921.1|516981_517434_+|PTS-sugar-transporter-subunit-IIA	gnl|CDD|334031	pfam00359, PTS_EIIA_2, Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2.	8.28808e-38
NZ_CP049862.1|WP_166412918.1|513838_514987_+|calcium:proton-antiporter	gnl|CDD|223464	COG0387, ChaA, Ca2+/H+ antiporter [Inorganic ion transport and metabolism].	3.11372e-62
NZ_CP049862.1|WP_166412927.1|525866_526568_+|demethylmenaquinone-methyltransferase	gnl|CDD|234689	PRK00216, ubiE, bifunctional demethylmenaquinone methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol methylase UbiE.	1.36649e-123
NZ_CP049862.1|WP_166412924.1|520046_521873_+|2-succinyl-5-enolpyruvyl-6-hydroxy-3--cyclohexene-1-carboxylic-acid-synthase	gnl|CDD|236020	PRK07449, PRK07449, 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase; Validated.	8.06781e-137
NZ_CP049862.1|WP_166412932.1|529897_531250_+|NADH-quinone-oxidoreductase-subunit-D	gnl|CDD|180385	PRK06075, PRK06075, NADH-quinone oxidoreductase subunit D.	0
NZ_CP049862.1|WP_166412919.1|515267_516029_+|DeoR/GlpR-transcriptional-regulator	gnl|CDD|224268	COG1349, GlpR, Transcriptional regulators of sugar metabolism [Transcription / Carbohydrate transport and metabolism].	2.09837e-78
NZ_CP049862.1|WP_166412934.1|532040_533384_+|NADH-quinone-oxidoreductase-subunit-NuoF	gnl|CDD|131014	TIGR01959, NADH-quinone_oxidoreductase_subunit_F, NADH-quinone oxidoreductase, F subunit. This model describes the F chain of complexes that resemble NADH-quinone oxidoreductases. The electron acceptor is a quinone, ubiquinone, in mitochondria and most bacteria, including Escherichia coli, where the recommended gene symbol is nuoF. This family does not have any members in chloroplast or cyanobacteria, where the quinone may be plastoquinone and NADH may be replaced by NADPH, nor in Methanosarcina, where NADH is replaced by F420H2. [Energy metabolism, Electron transport].	0
NZ_CP049862.1|WP_166412920.1|516025_516979_+|1-phosphofructokinase	gnl|CDD|238570	cd01164, FruK_PfkB_like, 1-phosphofructokinase (FruK), minor 6-phosphofructokinase (pfkB) and related sugar kinases. FruK plays an important role in the predominant pathway for fructose utilisation.This group also contains tagatose-6-phophate kinase, an enzyme of the tagatose 6-phosphate pathway, which responsible for breakdown of the galactose moiety during lactose metabolism by bacteria such as L. lactis.	6.01172e-109
NZ_CP049862.1|WP_166412917.1|512711_513674_-|1,4-dihydroxy-2-naphthoyl-CoA-synthase	gnl|CDD|181386	PRK08321, PRK08321, 1,4-dihydroxy-2-naphthoyl-CoA synthase.	0
NZ_CP049862.1|WP_166412933.1|531246_532044_+|NADH-quinone-oxidoreductase-subunit-NuoE	gnl|CDD|181024	PRK07539, PRK07539, NADH-quinone oxidoreductase subunit NuoE.	6.78475e-78
NZ_CP049862.1|WP_166412926.1|524491_525808_-|isochorismate-synthase	gnl|CDD|224091	COG1169, MenF, Isochorismate synthase [Coenzyme metabolism / Secondary metabolites biosynthesis, transport, and catabolism].	5.78858e-100
NZ_CP049862.1|WP_166412931.1|529172_529901_+|NADH-quinone-oxidoreductase-subunit-C	gnl|CDD|181115	PRK07785, PRK07785, NADH dehydrogenase subunit C; Provisional.	1.22435e-145

Protein sequences

>NZ_CP049862.1|WP_166412924.1|520046_521873_+|2-succinyl-5-enolpyruvyl-6-hydroxy-3--cyclohexene-1-carboxylic-acid-synthase
MTSPSATAARTLLAALVRLGVREVVLAPGSRSAPLAYAAAEAAEAGLLDLTVRVDEREAGFTAVGLVRGAALGGSHHRDVAPVAVVTTSGTAVANLHPAVLEAHHAGLPLLLLTADRPHEVRGTGASQTIDQPGIFGGAVRLAVDVPAPDGRPGEENDLVHLAARAVDAASGARSGFPGPVQLNLAFRDPLVPDADDATQWPDVRPPRVLPPPAASLDVSPWTAGELTDGGTLVVAGDGDDGSARRLAEARGWPLLAECVTPSAGGPRLVPAHAHVLAASPLTADVRRVVVVGRPTLSRPVQRLIAREDVDVVLVAPAGAPWADAPRGARTVLPEVPLGWFLPDAMLGDGLRTVRRDRWRDAWSAAGVAAAAAVDRALDLDRLGGGQGTATSAEGPGPLTAEAAVRILADALTPVDVLVVGSSNPVRDLDLVHRWTAQPRVVANRGVAGIDGLLSTAVGTALALGRPDRGGIEGRTVRALVGDLTFLHGAGGLAAARGEARPQLQVVVVNDAGGSIFTGLEHGALAESAPSRAAAVERVFGTPHDVDLGALCAAHGLPHVVVTDAAALRAALATPGRGTSVVEVRVDRDGRRARAAAVADALRTALAD
>NZ_CP049862.1|WP_166412923.1|519073_520039_+|o-succinylbenzoate-synthase
MHVYSIPLTTRFRRIDVREGVLLHGPGGWAEFSPFADYDDVESSSWLRAALEAAREAHPPAVRDRIPVNVTVPAVDGPRAHAVVRASGGCETAKVKVAEPGQSEADEIERLEAVRDALGPSGRIRIDANGGWDVATALARLTVLDRAAGGLEYVEQPCASVDDLAAVRRRTHVLVAADESIRRAEDPFEVVRREAADVVVLKVQPLGGVRACLRLAEEIGLPVVVSSALESSVGLADGLALAAALPELPYACGLATAHLLTDDTVVRPLVPVGGSIGVRRPVVAPAALARTAASDDVAAAWRDRLERCAAVLGEDLADVLG
>NZ_CP049862.1|WP_166412922.1|517430_518933_+|PTS-fructose-transporter-subunit-IIBC
MRFVAVTSCPTGIAHTYMAAEALEQTGKAQGHEVTVETQGSIGSEPLDPAVIAAADGVIFAADLEVKERDRFAGLPTVDVGVKRAVHDPAAVLAEAVAAVEAAAALPAAERPVAAPAPSRATSASGATRVRQWLMTGVSHMIPFVAAGGILIALSFMLAQVAWGGAEGAVEVTGADAAAIFASFDPLSLQHWSVVLLKTGQLAFGFLVPVLSGYIAYAIADRPGLVPGFVGGAAAGFIGAGFLGGLVTGFAAGFVALWISRWKVAKGVRGIMPVVVIPLLSSLVIGVLMLVLLGRPIAAAMDGLTDWLGGLQGGSIILLGALLGAMMGFDLGGPVNKVAYTFGVTGLATAGLTPDSPQYKVMAAVMLGGMVAPLALALATVVRPRLFTEVERENGKAAWLLGASFISEGAIPFAAADPWRVILASTVGSAVTGAVSMGMGVSLVAPHGGVWVLPLVGNALGFVVAILAGVAVACALVVLLKQTRRVPVAAAGPVLAGQDA
>NZ_CP049862.1|WP_166412921.1|516981_517434_+|PTS-sugar-transporter-subunit-IIA
MTSQLITADLVAIDLAAATKDVVIEALAERLAAAGRVTDGETFAADVRAREAQTPTGLPGQVGLPHAKSDAVLTPSLAVATVPGGVDFGGPDGPSTLVFLIAAPALGDNVHLQILAKLARKLMNAEFMASVRAATDGETLAALVNEAVTA
>NZ_CP049862.1|WP_166412920.1|516025_516979_+|1-phosphofructokinase
MIVTLTPNPSVDRAYDVEAVARGGVNRAGAVHVHPGGKGINVSRALAAHTVPTVAVLPVGGADGDLLVALLGATDVTVRAVPVPGDTRSNITLQESDGTTTKINAPGPVLDADGGARLLAAVVSAVGPGDTVVGAGSLPRGLAPDFYVTLADAVRERGARLVLDTSGAPLASAARAGGIALAKPNDDELAELVGRELATVGDVVEAAREILARGTDALLVSLGAHGALLVTADRSWWAGGPPLLPASTVGAGDTTLAGYLAAEHAGGDPATCLRTAVAWGRAAVLLPGTAVPGPDLVDVDAVTLTPDPAPTTPVKEM
>NZ_CP049862.1|WP_166412919.1|515267_516029_+|DeoR/GlpR-transcriptional-regulator
MYAPERQTEIVTRARNAGRVDVATLAAELDVAAETIRRDLGLLERRGLLRRVHGGAVPVERLALEPSVDERDLANTEAKDAIARAALTLLGDASTIVLDGGTTTARLAALLPEGRELTVITHALPVAAAVATRPGITLHLVGGHVRGRTLVATGPWTTAALAELRADVVVLGANGVSVDRGLTTPDLAEAEAKRALAAAGRRVVVLADHTKIGRDELVTFAPLERVDMLVTDAVVAPDLVAELVAAGVEVVTA
>NZ_CP049862.1|WP_166412918.1|513838_514987_+|calcium:proton-antiporter
MTTTSAPLVTRADIVRAGLGWVAYAVLLAVGGILEPPLPGPLLVAALVVIVGVVVVCAFGVVTQAEALAHRLGDPYGTLVLTLSIVIIEVVLIAAVMLGPGEHASIARDSVMAVSMIILNLVVGASLLVGGLRRGSLGHNRAGVSTYLALLVVLLALAFALPAYVGSEGSYSVVQAVPVVVLTVGLYAFFLQQQTGPRADDFREVDADVSPAAGEAPAPAPREPFARTLREHRREILTRLGLLVATVLPIVLLSHDMASLLDDGLGRLGAPVALAGVLIALIVFLPESLTSVRAALAGEGQRVSNLCHGALVSTVGLTIPVVLVIGMLTGQRVLLAESPANLVLLATTLLLSVATFSGRRATAVHGAVHLVLFGIYVLALLS
>NZ_CP049862.1|WP_166412917.1|512711_513674_-|1,4-dihydroxy-2-naphthoyl-CoA-synthase
MSEIPATVSETFDPQRWRTVAGFEDLVDMTYHRGVERTLGEDGSVTAERDLPVVRVAFDRPEVRNAFRPGTVDELYRILDHARLTSDVGTVLLAGNGPSPRDGGWAFCSGGDQRIRGRDGYRYAEGETADTVDPARAGRLHILEVQRLIRTMPKVVVAVVDGWAAGGGHSLHVVADLSIGCREHARFKQTDANVGSFDGGYGSAYLARQIGQKRAREIFFLAREYSAQDAYDWGALNEVAEHDDLEALALEYALTIARKSPQAIRMLKFAFNLADDGLMGQQVFAGEATRLAYMTDEAVEGRDAFLEHRDPDWSSYPYHV
>NZ_CP049862.1|WP_166415159.1|511705_512539_-|aldo/keto-reductase
MPTVTLHNGVEIPQLGLGVFQVPEDGTQALVEDALASGYRHIDTAAGYYNEEGVGAALAASGLPREDIFVTTKLRNGDQGFDKTLRAFESSRKALGVDVVDLYLIHWPVPSLDLYVETWRAFEKLYADGAVRAIGVSNFLPDHLDRLVAEAEILPVVNQVEVHPTLQQADVLANTLGHGIAVEAYSPLGRGKDLDDPAVAAIAARLGATPAQVILRWHLDAGRIVIPKSVTPERYRANLAAVELELTDADRAAIDALEEGNRLGAHPATAAFTQYRD
>NZ_CP049862.1|WP_166412916.1|511377_511602_+|hypothetical-protein
MTTTHAHHIPRPSGSDGAVRRVVRPSRTRRDHDSWRTSTAPAALSVALLTGLATALALGLREAVELALKFFVTG
>NZ_CP049862.1|WP_166412925.1|522138_523893_+|trypsin-like-serine-protease
MDENTTQPIPTAGDEPTHEGHAGTTDAQPTAPLPSAFAAPDGSTPRPVPPAPQPDPGQQPHAPYASAPQAAAPQVPAPQAPYGSQPTPAPQGVPYPPQGAHGAPTGAPYATASGPYAAPAAHNPYGQHPQGASFGPGAIPSPSVPRAPRKARTWPAVVATAAATALVVGGGSAYVTSQLVDSPAQSAAVSSSVHGLGKGSTISVDSVAPASWEEVAARVAPSVVAIDVVSQEGEAQGSGVIIDTSGHILTNNHVVSGAKNDTVTVTLSDGRLFDAKIVGVDASTDLAIVKLVTPPSDLTAATLADSDDVVVGNAVMAVGNPLGLANTVTTGIVSAVDRPVSTSDGTQASAAVTNAIQIDAAINPGNSGGPLFNAQGEVIGITSSIATLSSGSGQSGSIGLGFAIPSNLARSVGDQLIAKGVAQHAFLGVSLSDGTATADGSTRRGAQVVDVTAGSAAATGGVLKGDVIVAIDGKAVSGAEYLTAAVRERVGGDRAVLTVVRDGAAKDLTVTLTAKTDAAATPDSGSGSGDGSGSGSGSGDGSGSGNGDNTPGQGRPGRSNEGSEDSFPGGMTQDEFFQWLQENL
>NZ_CP049862.1|WP_166412926.1|524491_525808_-|isochorismate-synthase
MNANQPTPADHVPAGRVVVRTTALDLPDAATDPGALLDLLPADSPLSWVRRGDGIVAWGELARVEVGGEGQFAHAEQAWTRLLRTMTVHDDVRTPGTGPVAFGSFSFDPASPAGGALVVPRVVVGRRGPLAWVTTLAEETTSPAPQPTVAELLRVGAAPVTSPGPVTYADGALTPDAWLDVVADAVSRIRDGAVDKVVLARDVRARTTHPVDPRYLLGRLADRFSGCWTFSVDGLVGATPELLVRSEKGLVISRVLAGTVRRTGDDDADLARAAHLSHSSKDLEEHEYAVSSVAQALTPFCTSTNVPETPFVLHLPNVLHLATDVTGVLAAPGATSLALADALAPTAAVCGTPTSVARELIREIEHLDRARYAGAVGWLGADGDGEWGIGLRSAELDPEDPRELRLFAGCGIVAASVPADELAETEAKLEPMRYALGD
>NZ_CP049862.1|WP_166412927.1|525866_526568_+|demethylmenaquinone-methyltransferase
MSRASLEKKPREVASMFDGIARRYDLTNDVISLGQDRRWRRLTIDAVGAAPGEKVLDLAAGTGTSSEPFADEGVRVVPCDFSIGMLQVGKARRPDLSFTAGDATRLPFADASFDAVTISFGLRNVVDTVGALSEMLRVTRPGGRIVVCEFSSPTWAPFRTVYQEYLMKALPKVAGVVTKDAGSYEYLAESISSWPDQVALAHLMQEAGWRKVAYRNVSGGIVALHRATRPEAV
>NZ_CP049862.1|WP_166412928.1|526765_528061_+|geranylgeranyl-reductase-family-protein
MATNHPDDADVVVVGAGPAGATAAHYLASVGLDVVVLDKARFPRDKICGDGLTPRAVAELVRAGVSIDESDGWIRNIGLRVVGGGHRIEIPWPELSSYPSYGLARSRMSFDHLLVEHARKSGATVLEGMNVTEPVLDERTGRVVGVRARVLDADGRRTGEERTFRAPVVMAADGVSSRLATAVGIEKRNDRPMGVAVRTYFESPRHDDAWMESHLELWDGKPGESNLMPGYGWIFALGDGTVNVGLGSVSSSAAATKVDYKDLFQRWIANVPEEWGISEETQRGPVRGAALPMAFNRSPLYDRGLMLLGDAGGMVSPFNGEGIAYAMQAARVASDTVAQALTRPTDSARERALHRYAQVMRDDIGGYYRLGTYFVKLIENPHIMHLCTRYGLPRPLLMKFVMKLLSDGYESRGGDLMDRVIAGLTRVVPSA
>NZ_CP049862.1|WP_166412929.1|528233_528596_+|NADH-quinone-oxidoreductase-subunit-A
MSNPYVPLLFLMGVAAVLALGGVGASAIIGPKRYNKAKLEAYECGIEPTPHAIGGGRFPIKYYLVAMTFIIFDIEVVFLYPWAVEFRTLAVFGLVAILAFIAMITVPFIYEWRRGGFEWD
>NZ_CP049862.1|WP_166412930.1|528624_529176_+|NADH-quinone-oxidoreductase-subunit-B
MSNETAPSGFLLTTVEDFAGWARKSSIWPVTFGLACCAIEMMAAGASRFDLARYGMEVFRASPRQADLMIVAGRVSQKMAPIVRQVYDQMAEPKWVLSMGVCASSGGMFNNYAIVQGVDHVVPVDIYLPGCPPRPEMLINAINELQRQMQKEPLLTHRREVVKAVEAAALEATPTHQMKGLLR
>NZ_CP049862.1|WP_166412931.1|529172_529901_+|NADH-quinone-oxidoreductase-subunit-C
MSDEITPVGGEVAAAPAGALRGPDVVEVRAGLWGIHGTGDTSGFGGLVRQVAMPGSSARPYGGYFDEVVDVLLEVLEETEPGLAAKAVTGVVVDRDELTVEVAREHLVAVCRALRDDQDLRFELSLGVSGVHYPESTGRELRAVYHLTSVTHSRRVRLEVAAPDADPNIPSTVAIYPTNDWHERETWDFFGIVFDGHPALARIQMPDDWPGHPQRKDYPLGGIPVEYKGATIPSPDTRRSYS
>NZ_CP049862.1|WP_166412932.1|529897_531250_+|NADH-quinone-oxidoreductase-subunit-D
MSTATPHATRDAGKPADDNGVPSFEAYGDGDWSSIAEEAARLGEERIVVNMGPQHPSTHGVLRLMLEIDGETVTEARAGIGYLHTGIEKNMEFRTWTQGVTYCTRMDYLAPFFQEVAFCLGVEKLLGITDDIPERASQIRVLLMELNRVSSHLIAIGTGGNEMGATTVMTTSFTAREEILRLFEAVTGLRMNHGFVRPGGVPQDLPPGFVPEARAALVKVRHYIGQLELLMMENPIFKMRLVGVGQLNLAACMALGMTGPVLRSAGLPYDVRKTDPYCGYETYDFEVPVAQGADAYDRVVVRLAECHESLKIVDQVLERLEKGSGPVMVADKKIAWPAQMAIGTDGQGNSLDHIKEIMGTSMEALIHHFKLVTEGFRVPAGQVWQTVEAPRGELGVHLVSDGGTRPYRAHFRDPSFNNLQAVSMMCEGGQLADVVVAVASIDPVLGGVDR
>NZ_CP049862.1|WP_166412933.1|531246_532044_+|NADH-quinone-oxidoreductase-subunit-NuoE
MTTTGYAPEVRARLDADAAAVVSRYPQARSALLPLLHLVQSEDGYVSRHGIEFCAETLGLTTASVSAVATFYTQYKRRPNGEYTVGVCTNTLCAIMGGDEIFEQLSERLGVGHDETTEDGRITLERVECNAACDFAPVMMINWEFFDNQTADSALGVVDRLIAGEDVTPTRGPEKVVSFKEMSRVLAGFDDGLADQGVAAGGASLAGLEIAREHGWTAPSFDAGEREAVAAAAAAPADAAPGVGEEHSSADRPAPSDADVDIEEK
>NZ_CP049862.1|WP_166412934.1|532040_533384_+|NADH-quinone-oxidoreductase-subunit-NuoF
MMTSLTPILTRSWGDETPWQLASYEKAGGYEGLKKALGQSQTDLVQLVKDSGLRGRGGAGFPTGMKWGFLPAPDGGPRYLVVNADESEPGTCKDIPLMMADPHLLIEGVAITSYAIGSHHSFIYIRGEVVHVYRRLLKAVADAYAAGHLGKNIHGSGFDLDVTVHAGAGAYICGEETALLDSLEGRRGQPRLKPPFPAVAGLYARPTVVNNVESIASVPAIVRGGSDWFTSMGTERSTGHGIFSLSGHVTRPGQYEAPLGITLRELLEMAGGIRDGHRLKFWTPGGSSTPIFTDAHLDVPLDYESVGAAGSMLGTRALQIFDETTSVVRAVSRWTDFYAHESCGKCTPCREGTYWLKQILHRLEHGQGEAGDIEKLVDICDNILGRAFCALGDGATSSITSAVQLFREEFEAGMTQPASELFPPARSALFDYTPRRSAGAAAGAVHA

Crispr_ID: NZ_CP049862_8

• CRISPR_ID: NZ_CP049862_8
• CRISPR_location: 1180733-1180878
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP049862_8

Consensus_repeat	Method
CGTGCCTGGATCGGTCATCGAGCTCAGGGGCGCGCTCCTCGATAGCGGATCCCG	CRISPRCasFinder

spacers of NZ_CP049862_8

>8.1|1180787|38|NZ_CP049862|CRISPRCasFinder
TCACGTGAGGTGCACGGATCGGCTACCGAGCCACCTCA

CRISPR arrays and Neighbor proteins around NZ_CP049862_8

CRISPR arrays

The CRISPR arrays of NZ_CP049862_8

>merge|NZ_CP049862|8|1180733-1180878|CRISPRCasFinder
CGTGCCTGGATCGGTCATCGAGCTCAGGGGCGCGCTCCTCGATAGCGGATCCCGTCACGTGAGGTGCACGGATCGGCTACCGAGCCACCTCACGTGCCTGGATCGGTCACCGAGCTCAGGGGCGCGCTCCTCGATAGCGGATCCCG

>NZ_CP049862|8|8|1180733-1180878|CRISPRCasFinder
CGTGCCTGGATCGGTCATCGAGCTCAGGGGCGCGCTCCTCGATAGCGGATCCCG	TCACGTGAGGTGCACGGATCGGCTACCGAGCCACCTCA
CGTGCCTGGATCGGTCACCGAGCTCAGGGGCGCGCTCCTCGATAGCGGATCCCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP049862.1|WP_166413510.1|1176909_1177140_+|PTS-transporter-subunit-EIIB	unknown	unknown	gnl|CDD|238130
NZ_CP049862.1|WP_166413505.1|1171474_1173265_+|GTP-binding-protein-HSR1	unknown	unknown	gnl|CDD|206743
NZ_CP049862.1|WP_166413506.1|1173842_1174841_+|DUF4031-domain-containing-protein	unknown	unknown	gnl|CDD|226789
NZ_CP049862.1|WP_166413511.1|1177211_1178186_-|mechanosensitive-ion-channel-family-protein	unknown	unknown	gnl|CDD|223740
NZ_CP049862.1|WP_166413519.1|1189254_1189704_+|ribose-5-phosphate-isomerase	unknown	unknown	gnl|CDD|235509
NZ_CP049862.1|WP_166413518.1|1188381_1189092_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166413521.1|1190865_1192200_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|234945
NZ_CP049862.1|WP_166413514.1|1184730_1185375_+|DsbA-family-protein	unknown	unknown	gnl|CDD|376526
NZ_CP049862.1|WP_166413513.1|1181972_1184534_-|aminopeptidase-N	unknown	unknown	gnl|CDD|274121
NZ_CP049862.1|WP_166413508.1|1175499_1176363_-|acyl-CoA-thioesterase-II	unknown	unknown	gnl|CDD|224857
NZ_CP049862.1|WP_166413504.1|1169498_1171463_+|ABC-transporter	unknown	unknown	gnl|CDD|379062
NZ_CP049862.1|WP_166415214.1|1173408_1173837_+|acyl-CoA-thioesterase	unknown	unknown	gnl|CDD|223894
NZ_CP049862.1|WP_166415215.1|1181119_1181692_-|toxin	unknown	unknown	gnl|CDD|223637
NZ_CP049862.1|WP_166413507.1|1174931_1175489_+|deaminase	unknown	unknown	gnl|CDD|223340
NZ_CP049862.1|WP_166413509.1|1176364_1176748_-|globin	unknown	unknown	gnl|CDD|381280
NZ_CP049862.1|WP_166413517.1|1188210_1188381_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166413512.1|1178337_1180464_+|4-alpha-glucanotransferase	unknown	unknown	gnl|CDD|376788
NZ_CP049862.1|WP_166413520.1|1189721_1190837_+|Fpg/Nei-family-DNA-glycosylase	unknown	unknown	gnl|CDD|223344
NZ_CP049862.1|WP_166413515.1|1185371_1185953_+|hypothetical-protein	unknown	unknown	gnl|CDD|181433
NZ_CP049862.1|WP_166413516.1|1186098_1188099_-|peptidase-M13	unknown	unknown	gnl|CDD|226118

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP049862.1|WP_166413510.1|1176909_1177140_+|PTS-transporter-subunit-EIIB	gnl|CDD|238130	cd00212, PTS_IIB_glc, PTS_IIB, PTS system, glucose/sucrose specific IIB 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. This family is one of four structurally and functionally distinct group IIB PTS system cytoplasmic enzymes, necessary for the uptake of carbohydrates across the cytoplasmic membrane and their phosphorylation.	2.9696e-20
NZ_CP049862.1|WP_166413505.1|1171474_1173265_+|GTP-binding-protein-HSR1	gnl|CDD|206743	cd11383, YfjP, YfjP GTPase. The Era (E. coli Ras-like protein)-like YfjP subfamily includes several uncharacterized bacterial GTPases that are similar to Era. They generally show sequence conservation in the region between the Walker A and B motifs (G1 and G3 box motifs), to the exclusion of other GTPases. Era is characterized by a distinct derivative of the KH domain (the pseudo-KH domain) which is located C-terminal to the GTPase domain.	4.74529e-27
NZ_CP049862.1|WP_166413506.1|1173842_1174841_+|DUF4031-domain-containing-protein	gnl|CDD|226789	COG4339, COG4339, Uncharacterized protein conserved in bacteria [Function unknown].	2.29839e-34
NZ_CP049862.1|WP_166413511.1|1177211_1178186_-|mechanosensitive-ion-channel-family-protein	gnl|CDD|223740	COG0668, MscS, Small-conductance mechanosensitive channel [Cell envelope biogenesis, outer membrane].	6.50289e-38
NZ_CP049862.1|WP_166413519.1|1189254_1189704_+|ribose-5-phosphate-isomerase	gnl|CDD|235509	PRK05571, PRK05571, ribose-5-phosphate isomerase B; Provisional.	7.95715e-82
NZ_CP049862.1|WP_166413521.1|1190865_1192200_-|GNAT-family-N-acetyltransferase	gnl|CDD|234945	PRK01346, PRK01346, enhanced intracellular survival protein Eis.	1.79897e-94
NZ_CP049862.1|WP_166413514.1|1184730_1185375_+|DsbA-family-protein	gnl|CDD|376526	pfam01323, DSBA, DSBA-like thioredoxin domain. This family contains a diverse set of proteins with a thioredoxin-like structure pfam00085. This family also includes 2-hydroxychromene-2-carboxylate (HCCA) isomerase enzymes catalyze one step in prokaryotic polyaromatic hydrocarbon (PAH) catabolic pathways. This family also contains members with functions other than HCCA isomerisation, such as Kappa family GSTs, whose similarity to HCCA isomerases was not previously recognized. Some members have been annotated as dioxygenases, dehydrogenases, or putative glycerol-3-phosphate transfer proteins, but are most likely HCCA isomerase enzymes.	3.60706e-08
NZ_CP049862.1|WP_166413513.1|1181972_1184534_-|aminopeptidase-N	gnl|CDD|274121	TIGR02412, Aminopeptidase_N, aminopeptidase N, Streptomyces lividans type. This family is a subset of the members of the zinc metallopeptidase family M1 (pfam01433), with a single member characterized in Streptomyces lividans 66 and designated aminopeptidase N. The spectrum of activity may differ somewhat from the aminopeptidase N clade of E. coli and most other Proteobacteria, well separated phylogenetically within the M1 family. The M1 family also includes leukotriene A-4 hydrolase/aminopeptidase (with a bifunctional active site).	0
NZ_CP049862.1|WP_166413508.1|1175499_1176363_-|acyl-CoA-thioesterase-II	gnl|CDD|224857	COG1946, TesB, Acyl-CoA thioesterase [Lipid metabolism].	3.05096e-95
NZ_CP049862.1|WP_166413504.1|1169498_1171463_+|ABC-transporter	gnl|CDD|379062	pfam13191, AAA_16, AAA ATPase domain. This family of domains contain a P-loop motif that is characteristic of the AAA superfamily.	0.00981687
NZ_CP049862.1|WP_166415214.1|1173408_1173837_+|acyl-CoA-thioesterase	gnl|CDD|223894	COG0824, FcbC, Predicted thioesterase [General function prediction only].	3.98685e-21
NZ_CP049862.1|WP_166415215.1|1181119_1181692_-|toxin	gnl|CDD|223637	COG0563, Adk, Adenylate kinase and related kinases [Nucleotide transport and metabolism].	1.50144e-20
NZ_CP049862.1|WP_166413507.1|1174931_1175489_+|deaminase	gnl|CDD|223340	COG0262, FolA, Dihydrofolate reductase [Coenzyme metabolism].	4.01216e-10
NZ_CP049862.1|WP_166413509.1|1176364_1176748_-|globin	gnl|CDD|381280	cd14771, TrHb2_Mt-trHbO-like_O, Truncated hemoglobins, group 2 (O); Mycobacterium tuberculosis hemoglobin O like. The M- and S families exhibit the canonical secondary structure of hemoglobins, a 3-over-3 alpha-helical sandwich structure (3/3 Mb-fold), built by eight alpha-helical segments. Truncated hemoglobins (TrHbs, 2/2Hb, or 2/2 globins) or the T family globins adopt a 2-on-2 alpha-helical sandwich structure, resulting from extensive and complex modifications of the canonical 3-on-3 alpha-helical sandwich that are distributed throughout the whole protein molecule. TrHbs are classified into three main groups based on their structural properties and named after Mycobacterium sp. genes glbN, glbO, and glbP: TrHb1s (N), TrHb2s (O) and TrHb3s (P). This group includes a Mycobacterium tuberculosis TrHb2, Mt-trHbO, encoded by the Mycobacterium tuberculosis glbO gene, which is expressed throughout the Mycobacterium growth phase. It also includes a TrHb2 from the thermophilic Thermobifida fusca ( Tf-trHb) which has a high thermostability and at the optimal growth temperature for Thermobifida fusca (between 55 and 60 degrees C ), it is capable of efficient O2 binding and release. Tf-trHb shares a relatively slow rate of oxygen binding with Mt-trHbO.	1.62337e-61
NZ_CP049862.1|WP_166413512.1|1178337_1180464_+|4-alpha-glucanotransferase	gnl|CDD|376788	pfam02446, Glyco_hydro_77, 4-alpha-glucanotransferase. These enzymes EC:2.4.1.25 transfer a segment of a (1,4)-alpha-D-glucan to a new 4-position in an acceptor, which may be glucose or (1,4)-alpha-D-glucan.	8.53901e-153
NZ_CP049862.1|WP_166413520.1|1189721_1190837_+|Fpg/Nei-family-DNA-glycosylase	gnl|CDD|223344	COG0266, Nei, Formamidopyrimidine-DNA glycosylase [DNA replication, recombination, and repair].	5.0409e-39
NZ_CP049862.1|WP_166413515.1|1185371_1185953_+|hypothetical-protein	gnl|CDD|181433	PRK08455, fliL, flagellar basal body-associated protein FliL; Reviewed.	0.0010721
NZ_CP049862.1|WP_166413516.1|1186098_1188099_-|peptidase-M13	gnl|CDD|226118	COG3590, PepO, Predicted metalloendopeptidase [Posttranslational modification, protein turnover, chaperones].	0

Protein sequences

>NZ_CP049862.1|WP_166413512.1|1178337_1180464_+|4-alpha-glucanotransferase
MDNAERSESLLRLASACGVGTEYWAFDGTERHVAAETLVKVLGALGIDASTPTRVELALLHVEDDAWREPLPPTVVAREGQAVTIPVHVPDGTSVSVWIDVDPEAGGGRREARQVDNWDAPRRVDGRMVGRASFEIPSDLPLGWHTLRSRADDGEHVATLIVTPQRLHLPNDLEHGRVWGLMSQMYSVRSSRSWGVGDFADLAETSWFAGRDLGANFMLINPVHAGEPSAPMTPSPYLPVTRRFVNPLYVRPEAVEEAAYLTAADRSLVEWAAEEAQTLNASSGPIDRDAAWTHKRSALEVIFSAPRTAIREAQLADFRDREGKGLEDFALWCAIKELHPTGAWPDELWDHASPEVAELRIELADRVDFFVWLQWVADSQLAAAQAAAKAGGMSLGIMHDLAVGVHPEGSDAWSLRHALATAASVGAPPDMYNQQGQDWSQPPWHPKGLARVGYQPYREMLRTVLRHAGAIRIDHVIGLFRLWWIPAGSGAKEGAYVRYDHDAIIGILCLEAQRAGAVVIGEDLGTFEGWVRDYLTERGILGTSILWFEKDHDGRPLAPEHYRAMSLTSVTTHDLPPTAGYLAGEHVELRESLGLLQAPVQEVRNEARAERDDMVRLLAARGLLGDDPSERELVEALHRLIKLTPSKILGVSLADAVGERRAQNQPGTDQEYPNWKIPLGDPNGVTVLLDDLVTNPRLRSLAAAMNQR
>NZ_CP049862.1|WP_166413511.1|1177211_1178186_-|mechanosensitive-ion-channel-family-protein
MLDHLPRATTNPTPSPTGTSVGDEIGDALTKAPGERSGWVDWLVGAPLRIVVIIVIGIVLLVVLRRIIASFTERIAREPRTDLGGALLRVTNALEDERRAGRARTLGSVLRSTISIVIGSIVVMMVLNELGVNLAPLLASAGVAGVALGFGAQSLVKDFLSGIFMLAEDQYGVGDTVSFVDVTGTVEEVALRVTKVRDLDGTLWYLRNGEILRTGNLSQGWVRAMADFRVPYDVDTNHVRSLLTQAAEETAADDDISPVLLAPPEVFVVELTDDHLLYRLQARTNLSDRAAVVRALRTRGLEALTSGGIKLVTANRLVVQPPRT
>NZ_CP049862.1|WP_166413510.1|1176909_1177140_+|PTS-transporter-subunit-EIIB
MSKAEKILTALGGGSNVVDLEPCITRLRVEVTDPSLVDEAKLKETGAFGVVRSGRIIQVIVGPEADDLADELETLR
>NZ_CP049862.1|WP_166413509.1|1176364_1176748_-|globin
MTEQTFYDAVGGHDTFQGIVDRFYAGVVADDVLAPMYPPEDLPGANRRMVTFLEQYWGGPTTYSEERGHPRLRMRHQPFKVNPLARDRWIQHMVAAVKDARLSPLHESQLLDYLERAAHSMLNTFED
>NZ_CP049862.1|WP_166413508.1|1175499_1176363_-|acyl-CoA-thioesterase-II
MTDAAPFTALRDVLALEQIDENTFAGQSLPQLNGRVYGGQVLAQALLAAGATNPAGRQPHSLHGYFLRPGALDVPIRFEVERLRDGRSFSARRVHAIQGDTAILSMITSAQEDQPGIDQQQPMPAAPDPETLESAVAKLSTIEHPVARFWTSTAAFDVRHVGTSLYLGPDRDGDDRQMVWLRARGTLGDDQLMHRAMMIYACDQLMLEPVMRRADLDWGTRGLSIASLDHAMWWHRDARADEWLLYVQSSPSAQGGRGLGSARVFAQDGTLVASIAQEGMVRVPDAD
>NZ_CP049862.1|WP_166413507.1|1174931_1175489_+|deaminase
MRTLRYSINVTLDGCVHHEAGVAPDAELMQFWTADTERADVLLFGRVTYQMMEEAWRRPTDGVWPDWMSAWEVPFAESIDAKPKLVVSSTLGSVDWNAELLRGDLIESVRRLKEGPGGDLSVGGVRLPLALANAGLIDEYVFVLHPVVAGHGPTLLAGLDELVRLEQVDRQPFASGAVAHTFRPA
>NZ_CP049862.1|WP_166413506.1|1173842_1174841_+|DUF4031-domain-containing-protein
MAVLVDAPSWAAHGTTWAHLVSDASLDELHAFAERAGVPRRAFDLDHYDVPAERHAELVALGAEPVSAREMVVRLAASGLRVTGRDRARARRADLAERWATLLPGADAVGEELLRRWSEPHRTYHGTAHLADCLRSVQVAAEGQGPVPQTVLLALWFHDAVHDGEAVRDEERSAALARDLLAPYVGTPGRVPDGSVVTRRDDDATALPVGDPSRVPAVLTRDDVDEVARLVLLTTHHDPAPDDLAGALVSDADLAVLAGAPAEYEKYVRQVRAEYAHVDDAAWRVGRGEVLRGLLAAPRLFATPFGRDRWEARARANLAAELAVLEAPGGAA
>NZ_CP049862.1|WP_166415214.1|1173408_1173837_+|acyl-CoA-thioesterase
MDAYAHVNNVEMLRLLEEARIEAFWRHPETDGVVSRPTAILDASPGASTATLVAHQEIEYLAPLTYQRQPVTVRLWLGRLGGASLEIHYEVTDASSTVYARAITTMVLVDAASGSPRRIDADERAAWEPFLDEPVAMRRRAR
>NZ_CP049862.1|WP_166413505.1|1171474_1173265_+|GTP-binding-protein-HSR1
MTLAGRLDALEDAWTTAEPWLDGGDGTTRPTTRPTPITSTSTTPSTPTGTTPSASPAGTRAGLTEVPVVVARVRERLGLGADRTVVALAGSTGSGKSSLLNALAGAEVARPGLLRPTTSQPVAASADGSDPTTLLDWLDVRERTHLPESSPLPAGIVLLDLPDHDSVEVAHRVRADRLLERADVMVWVTDPQKYADAALHDDYLRPLAAYGGVAVVVLNHADRLAAADVARVLADLRRRVDDDGLAGAHVLATSATTGAGLPELRTVLAEAARRRERDAARLVVDVRRAATLLLEASGGTDRAARAAAPSEDALVAALAGAAGAGTVVDAVGASTRRQIHLTAGWPVTRWLAGFRADPLGRLGLGAGRTLERASGPGAERRPDARGRRARSEVADPTVETVRSSLPRPSDAVRARAALAVREHVAGALDALPDAWRPAASDRVDGARLADALDTAVVGARLGVDRAPRWARALGVVQMLLLGVVVVGLAWVLGVRGLAYLGVTLPLPELVLDGPSGQVRFAWPAVLVVGGVVLGLLLALVASLCGRATAARRARRARRRLDEAVATVARSTVLAPLGARLDALSRTRDLATTAATP
>NZ_CP049862.1|WP_166413504.1|1169498_1171463_+|ABC-transporter
MDDDARGSAGPRPDRVALTVALEAARDAVGALALPLATPGRETSEALRRATLARLDDHLLPRSRAEGAPVLVVVGGSTGAGKSTLVSSVVGAPVSAAGVLRPTTLAPVLVHHPDDAAWFGADRVLPHLVRARADEPVPAEAVHRTLRLVPTEAVGPGIALLDAPDVDSVVAANRDLAAQLLGAADLWLFVTTAARYADAVPWALLDSAARRRTRLALVLDRVEGAGAGAVAEHLRSMLAEHGLAGTPVIEVPESPLVEGLLGEGALVDLRGWFADVGTAAARERVVRETFDGAVDDVVHVLDELAAAAAEQADAAARLEEAVAHAYGRALDDVAAVTADGTMLRGEVLARWQDLVGTGDLVRRIEQGVGRVRDRLGAFVRGRRADAPAAVRAVGHDLEAVIVDAVHAAAERASDAWRADPAGRALTDGLVRGGPALREDAAAAVRGWQDDVLELVRTTGSSKRGTARALSFGVNGLGLALMVVVFASTGGLTGAEVGIAGGTALVAQRLLEAVFGDDAVRRLAVTARTRLVERVTAVADADAARFRARLHEALGTRGRDAVGEPLHDGAGVPQHDAAGLPQHDASAGRPAGTPPTTPGAGRLDAAAHRVREAAAVERSTRPLPPVPEPPTMPEASPDAVEDEPLKRPWWRRGRA
>NZ_CP049862.1|WP_166415215.1|1181119_1181692_-|toxin
MRRTPTPRRIRILGTSGSGKTTLARAVAARTGLVRIELDEVFWDVDWQQKDAEAGRSLLRSRLAAAESGPGWVVDGSWQSKVLDLLDGAETIVCLDLPRRTVTRRVVTRTLARGLTRRPLWHGNRESLTNLVRRRPEDNIVLWSWQTWAGNRRRWDELEAAGAPVVRLRSPREVRTWLASLPRALEVPTD
>NZ_CP049862.1|WP_166413513.1|1181972_1184534_-|aminopeptidase-N
MPGQNLTRAEAIERASVVQTQSYDITLDLTTGPTTFASTSTVRFTATPGASTFIDLVAPTVRTVTLNGRELDPAVVFADSRIALDGLEADNELTVVADGAYTNTGEGLHRFVDPVDGEVYLYTQFEVPDSRRVFAVFEQPDLKATFAFTVTAPEAWQVVSNEPTPEPTVAGGSATYAFPATPRISSYITALVAGPYAVMRSELTSADGRTIPLGVFCRASLAEHMDADYVFDTTRAGFEFFEKSFEQPYPFTKYDQLFVPEYNMGAMENAGCVTFTESYVFRSKVTDAIKERRVVTILHELAHMWFGDLVTMRWWNDLWLNESFAEWASTLATAEATEWKGAWTTFAAMEKSWAYRQDQLPSTHPIVAEIRDLEDVQVNFDGITYAKGGSVLKQLAAWVGLEAFLKGVAEYFRKHAWGNTELSDLLVELEAASGRDLKSWSTLWLETAGVNTLRPEITVDDAGVVTGFAILQSAPADYPTIRPHRLAVGYYTLTDDGLVRTHRLELDVDGERTEVPELVGTTRPDLVLLNDDDLAYAKIRLDDASRAAAIENLALISDPLARSLVWGSIWDATRDGEVPASDFVRLVLNNIAAETESTTIRTTLNQLLLAASSYVAPERSEATLVAVGDGLLAMARTAEAGSDAQFQFVKFLAQVARTDAQLDAVAALRDGSETLEGLTIDTDLRWELLIALVAGGRATAAQIDAALVDDDTASGRQQAAHARAALPTVEAKAAAWASIVDDADKPNAIIRATALGFNHVLDASILESFIATYHDALFPIWESRTYHMSEELIEGLYPAPLANEALRAATQTWLDAHAEGSSKVAPPALRRFVVEGLAGIERALTAQAVDAQA
>NZ_CP049862.1|WP_166413514.1|1184730_1185375_+|DsbA-family-protein
MHDDNATTVADMWFDPACPWAWMTSRWLTEVRELRGITIRWHVMSLSVLNEGRDLPAEYREMLDASWGPVRVLVAAALRHGDDVLGPLYTAIGTKFHVDGDKDRRAVVATALADAGLDADLLDVWDTTDVDDALRASHQSALDLVGDEVGTPVVAIGGVGYFGPVVTPAPRGEDALRLWDGLVLMTQVPGFYELKRTRTSGPVLRPEEAQGADA
>NZ_CP049862.1|WP_166413515.1|1185371_1185953_+|hypothetical-protein
MTIPVPVGPPAKRPLGPGIIAFIVVDVVLVLGVVIAAIILLGGGNDPDRAPGASSTTPAPGVTTSSAPTTSVDRPGGTDQRFATPSGNIVCDITAAGARCGIASLAQKPAPVDGCDGSVGYVYVVDASGKVDVPCVPKKDLPKKGGSDVNVLGYGQRSSAFGFTCTSEESGMACVDDVTGSGFSLARAGGRVV
>NZ_CP049862.1|WP_166413516.1|1186098_1188099_-|peptidase-M13
MTTDNTAALRSGIDASTFDADVRPQDDLFRHVNGRWLTTYEIPADRARDGAFRELHDRAEEQVRDIILEAGEQAGAEGVDATTAKIGALYASFMDTERIAALGTAPLAADLTLLDTTDKVALARGLGELQRTGAAGALGLYVDNDALDPESYVVYLYQAGLGLPDEAYYREEQHAEALAAYGPHVARMLTLGGIVPAAEADAAAARVVALETALATHHWDVVRDRDAELTYNPLTFAALAASAPGLDWDAWAAGLGAPAGSLDNVVMREPSFATGLAALWEQTDVADLRLWLAAQVVSSRAAYLTDEIVEANFDFYGRTLTGAEEIRERWKRGVSIVEGALGEAVGQVYVERHFPAAHKEHMDRLVGHLVEAYRESITGLEWMGEETKVKALAKLDAFTPKIGYPVRWRDYASLEIDAADLVGNVRRASVFETDRELSKIGKPLDRDEWFMTPQTVNAYYNPGMNEIVFPAAILQPPFFDPEAEDAVNFGGIGGVIGHEIGHGFDDQGSKYDGSGRLEDWWTEEDRSKFEERTKALIAQYDAFSPAQLGDEHTVNGALTIGENIGDLGGLSIALKAYRIALGGDLASAPEIDGLTGLQRVFLGWGQVWRTKARDAEAIRLLAIDPHSPAEFRCNGIVSNVDEFYEAFDVTEGDALHLAPEARVRIW
>NZ_CP049862.1|WP_166413517.1|1188210_1188381_+|hypothetical-protein
MPDRELDALAERVRTVPAWRRALGWCCPCCVAVEHLPDDLAAAVRAGDTTSRGTVR
>NZ_CP049862.1|WP_166413518.1|1188381_1189092_-|hypothetical-protein
MDLSRPLPVALLAVLAVVTVAVLVVVALVARQLTRRTRIAVGGTAAVLALGILGTGWYAWSTSSHHDTIDVNALGPGSGLTLNLKHDRLSKSGDEYDFALLRGTDADDVHDALVATGTPVDPVPGGWTLVKGGLRYSVVMRDDGTWHAENKTLTVAHGNDLTSIAFPTTADLYRADVGTPVRLPVPAAGVRAELELLGADADGPDTLVVPTNDGRTARLTFEGDLMTVEVVGAPRN
>NZ_CP049862.1|WP_166413519.1|1189254_1189704_+|ribose-5-phosphate-isomerase
MRVHLASDHAGFALKSHLLTHLAAQGHDVVDHGAFEYDAEDDYPAFCIAAGEAVVAEPGSLGIVIGGSGNGEQIAANKVDGVRAALAWSVETAKLGRQHNDANVIAIGERQHTIEEATTFVEAFLAEPFSGVERHQRRIDQLAAYESAR
>NZ_CP049862.1|WP_166413520.1|1189721_1190837_+|Fpg/Nei-family-DNA-glycosylase
MPEGHTVHRLARTFDALFAGEPLRLSSPQGRFAAGAALLDGGTLVRAEAWGKHMFLGFGPGATTPGTTTSDADLAWLRVHLGLYGSWTFAGDGSTTVAHAIGAPRRRIGEQEHALTAAPPAAPPATAAPADGPRSADEPPSADLVLSSRDSAAERLGRAAGTSSREGWVLPEPRGQVRVRIVGEHAVADLTGPSACEVITDTERHDVLARLGPDPIRADADPERFVARVRRSRTAVGLQLMAQDVVAGVGNIFRAEALFRAGLDPQTPGNVVPAETLREIWDDLVVLMRDGVATGRIVTTRPEHRGLGHEKGRMDPRRVRQNTDGDPDVVSREESFYVYHRDGLACRVCGATILVRDAAGRTLFWCPACQR
>NZ_CP049862.1|WP_166413521.1|1190865_1192200_-|GNAT-family-N-acetyltransferase
MSIPHGYRTQQLDESFREAAFTLDTWAFPSGTSPEDWAEIEFPMDWSRFVGVVEDGPDPDAVPIDGAAPARSDLVAMYGSYAFDRFPVPGAETAVGGLTWVGVHPQHRRRGILRGMITDHLDACAERGENVSALFAAEAGIYGRFGYGLASHDVRLNIPRGATLRDVPGAGTHTVRIEVADADRHGELVESVHREAGRRPLGVDGPHGALLNRPGWVGRDDPALARRMLLDPPAWRDGKEARRIVIVERDGEPRGFATFRRSSEWTDDGPRGTVHLGEVATLDAAAAHDLWAVLLDLDLMAKVSTFLLPPDDAILGLLLDPRSAGTKRVDNVWVRIVDVAGALAARRYQADVDVVLHVTDELRPASTGSYRVRATAFAEPEATRTHDDADLGLDVAALGAAYLGGQTLAALGLAGRVTELRPGALALASGAFGWPVAPSSSFVF

Crispr_ID: NZ_CP049862_9

• CRISPR_ID: NZ_CP049862_9
• CRISPR_location: 2325823-2325939
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP049862_9

Consensus_repeat	Method
CGCGACCCCCGCGACCGCGCCCT	CRISPRCasFinder

spacers of NZ_CP049862_9

>9.1|2325846|31|NZ_CP049862|CRISPRCasFinder
ACGCGCAGCGCGCCGCGACCCGCACGGACGC
>9.2|2325900|17|NZ_CP049862|CRISPRCasFinder
AGAACGTCGAGAAGCTT

CRISPR arrays and Neighbor proteins around NZ_CP049862_9

CRISPR arrays

The CRISPR arrays of NZ_CP049862_9

>merge|NZ_CP049862|9|2325823-2325939|CRISPRCasFinder
CGCGACGCCCGCGACCGCGCCCTACGCGCAGCGCGCCGCGACCCGCACGGACGCCGCGGCCGCCGCGACGGCCACGGAGAACGTCGAGAAGCTTCGCGGCCCCGCCGCACGCGTCGT

>NZ_CP049862|9|9|2325823-2325939|CRISPRCasFinder
CGCGACGCCCGCGACCGCGCCCT	ACGCGCAGCGCGCCGCGACCCGCACGGACGC
CGCGGCCGCCGCGACGGCCACGG	AGAACGTCGAGAAGCTT
CGCGGCCCCGCCGCACGCGTCGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP049862.1|WP_166414371.1|2335738_2337466_+|nitrite/sulfite-reductase	unknown	unknown	gnl|CDD|223233
NZ_CP049862.1|WP_166414363.1|2322152_2323256_+|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|182539
NZ_CP049862.1|WP_166415321.1|2319906_2321241_-|HlyC/CorC-family-transporter	unknown	unknown	gnl|CDD|224173
NZ_CP049862.1|WP_166414358.1|2312705_2314046_+|APC-family-permease	unknown	unknown	gnl|CDD|129987
NZ_CP049862.1|WP_166415322.1|2330553_2331141_+|lysophospholipase	unknown	unknown	gnl|CDD|238873
NZ_CP049862.1|WP_166414372.1|2337462_2338368_+|phosphoadenylyl-sulfate-reductase	unknown	unknown	gnl|CDD|234997
NZ_CP049862.1|WP_166414357.1|2312118_2312601_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166414359.1|2314208_2316956_+|bifunctional-acetaldehyde-CoA/alcohol-dehydrogenase	unknown	unknown	gnl|CDD|237515
NZ_CP049862.1|WP_166414370.1|2334279_2335416_-|succinyldiaminopimelate-transaminase	unknown	unknown	gnl|CDD|236119
NZ_CP049862.1|WP_166414367.1|2329485_2330466_+|aldo/keto-reductase	unknown	unknown	gnl|CDD|381312
NZ_CP049862.1|WP_166414374.1|2339364_2340696_+|sulfate-adenylyltransferase	unknown	unknown	gnl|CDD|180120
NZ_CP049862.1|WP_166414360.1|2317089_2318538_-|hypothetical-protein	unknown	unknown	gnl|CDD|350615
NZ_CP049862.1|WP_166414361.1|2318860_2319910_-|HlyC/CorC-family-transporter	unknown	unknown	gnl|CDD|224173
NZ_CP049862.1|WP_166414365.1|2324236_2325055_+|ABC-transporter-permease-subunit	unknown	unknown	unknown
NZ_CP049862.1|WP_166414364.1|2323298_2324240_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213235
NZ_CP049862.1|WP_166414362.1|2321403_2322150_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_CP049862.1|WP_166414368.1|2331210_2332296_-|PilT/PilU-family-type-4a-pilus-ATPase	unknown	unknown	gnl|CDD|225364
NZ_CP049862.1|WP_166414373.1|2338364_2339309_+|sulfate-adenylyltransferase-subunit-CysD	unknown	unknown	gnl|CDD|235375
NZ_CP049862.1|WP_166414375.1|2341023_2342307_+|uroporphyrinogen-III-C-methyltransferase	unknown	unknown	gnl|CDD|381169
NZ_CP049862.1|WP_166414369.1|2332723_2334022_-|citrate-synthase	unknown	unknown	gnl|CDD|99867

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP049862.1|WP_166414371.1|2335738_2337466_+|nitrite/sulfite-reductase	gnl|CDD|223233	COG0155, CysI, Sulfite reductase, beta subunit (hemoprotein) [Inorganic ion transport and metabolism].	4.23546e-163
NZ_CP049862.1|WP_166414363.1|2322152_2323256_+|HAMP-domain-containing-protein	gnl|CDD|182539	PRK10549, PRK10549, two-component system sensor histidine kinase BaeS.	1.45638e-58
NZ_CP049862.1|WP_166415321.1|2319906_2321241_-|HlyC/CorC-family-transporter	gnl|CDD|224173	COG1253, TlyC, Hemolysins and related proteins containing CBS domains [General function prediction only].	8.11857e-107
NZ_CP049862.1|WP_166414358.1|2312705_2314046_+|APC-family-permease	gnl|CDD|129987	TIGR00909, putative_amino_acid_transporter, amino acid transporter. [Transport and binding proteins, Amino acids, peptides and amines].	1.10862e-37
NZ_CP049862.1|WP_166415322.1|2330553_2331141_+|lysophospholipase	gnl|CDD|238873	cd01835, SGNH_hydrolase_like_3, 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.	2.84485e-52
NZ_CP049862.1|WP_166414372.1|2337462_2338368_+|phosphoadenylyl-sulfate-reductase	gnl|CDD|234997	PRK02090, PRK02090, phosphoadenylyl-sulfate reductase.	1.41465e-90
NZ_CP049862.1|WP_166414359.1|2314208_2316956_+|bifunctional-acetaldehyde-CoA/alcohol-dehydrogenase	gnl|CDD|237515	PRK13805, PRK13805, bifunctional acetaldehyde-CoA/alcohol dehydrogenase; Provisional.	0
NZ_CP049862.1|WP_166414370.1|2334279_2335416_-|succinyldiaminopimelate-transaminase	gnl|CDD|236119	PRK07865, PRK07865, N-succinyldiaminopimelate aminotransferase; Reviewed.	0
NZ_CP049862.1|WP_166414367.1|2329485_2330466_+|aldo/keto-reductase	gnl|CDD|381312	cd19086, AKR_AKR11C1, AKR11C family of aldo-keto reductase (AKR). Bacillus subtilis uncharacterized oxidoreductase YqkF is a founding member of aldo-keto reductase family 11 member C1 (AKR11C1). It may function as oxidoreductase. This family also includes Bacillus halodurans AKR11C1, an NADPH-dependent 4-hydroxy-2,3-trans-nonenal reductase.	2.33965e-93
NZ_CP049862.1|WP_166414374.1|2339364_2340696_+|sulfate-adenylyltransferase	gnl|CDD|180120	PRK05506, PRK05506, bifunctional sulfate adenylyltransferase subunit 1/adenylylsulfate kinase protein; Provisional.	0
NZ_CP049862.1|WP_166414360.1|2317089_2318538_-|hypothetical-protein	gnl|CDD|350615	cd14814, Peptidase_M15, Metalloproteases including zinc D-Ala-D-Ala carboxypeptidase, L-Ala-D-Glu peptidase, L,D-carboxypeptidase, bacteriophage endolysins, and related proteins. This family summarizes zinc-binding metallopeptidases which are mostly carboxypeptidases and dipeptidases, and includes zinc-dependent D-Ala-D-Ala carboxypeptidases, VanX, L-Ala-D-Glu peptidase, L,D-carboxypeptidase and bacteriophage endolysins, amongst other family members. These peptidases belong to MEROPS family M15 which are involved in bacterial cell wall biosynthesis and metabolism.	1.48361e-27
NZ_CP049862.1|WP_166414361.1|2318860_2319910_-|HlyC/CorC-family-transporter	gnl|CDD|224173	COG1253, TlyC, Hemolysins and related proteins containing CBS domains [General function prediction only].	3.33027e-83
NZ_CP049862.1|WP_166414364.1|2323298_2324240_+|ATP-binding-cassette-domain-containing-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.	1.16164e-91
NZ_CP049862.1|WP_166414362.1|2321403_2322150_+|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].	1.62755e-84
NZ_CP049862.1|WP_166414368.1|2331210_2332296_-|PilT/PilU-family-type-4a-pilus-ATPase	gnl|CDD|225364	COG2805, PilT, Tfp pilus assembly protein, pilus retraction ATPase PilT [Cell motility and secretion / Intracellular trafficking and secretion].	5.53355e-151
NZ_CP049862.1|WP_166414373.1|2338364_2339309_+|sulfate-adenylyltransferase-subunit-CysD	gnl|CDD|235375	PRK05253, PRK05253, sulfate adenylyltransferase subunit CysD.	0
NZ_CP049862.1|WP_166414375.1|2341023_2342307_+|uroporphyrinogen-III-C-methyltransferase	gnl|CDD|381169	cd11642, SUMT, Uroporphyrin-III C-methyltransferase (also known as S-Adenosyl-L-methionine:uroporphyrinogen III methyltransferase, SUMT). SUMT is an enzyme of the cobalamin and siroheme biosynthetic pathway. It catalyzes the first of three steps leading to the formation of siroheme from uroporphyrinogen III; it transfers two methyl groups from S-adenosyl-L-methionine to the C-2 and C-7 atoms of uroporphyrinogen III to yield precorrin-2 via the intermediate formation of precorrin-1. Precorrin-2 is also a precursor for the biosynthesis of vitamin B12, coenzyme F430, siroheme and heme d1. This family includes proteins in which the SUMT domain is fused to other functional domains, such as to a uroporphyrinogen-III synthase domain to form bifunctional uroporphyrinogen-III methylase/uroporphyrinogen-III synthase, or to a dual function dehydrogenase-chelatase domain, as in the case of the multifunctional S-adenosyl-L-methionine (SAM)-dependent bismethyltransferase/dehydrogenase/ferrochelatase CysG, which catalyzes all three steps that transform uroporphyrinogen III into siroheme.	1.86234e-97
NZ_CP049862.1|WP_166414369.1|2332723_2334022_-|citrate-synthase	gnl|CDD|99867	cd06114, EcCS_like, Escherichia coli (Ec) citrate synthase (CS) GltA_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). 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. There are two types of CSs: type I CS and type II CSs. Type I CSs are found in eukarya, gram-positive bacteria, archaea, and in some gram-negative bacteria and are homodimers with both subunits participating in the active site. Type II CSs are unique to gram-negative bacteria and are homohexamers of identical subunits (approximated as a trimer of dimers). Some type II CSs including EcCS are strongly and specifically inhibited by NADH through an allosteric mechanism. Included in this group is an NADH-insensitive type II Acetobacter acetii CS which has retained many of the residues used by EcCS for NADH binding.	0

Protein sequences

>NZ_CP049862.1|WP_166414365.1|2324236_2325055_+|ABC-transporter-permease-subunit
MMRAVRLEVAKFFSTRMWWVLLILMGGYMALLAGGMGFAFTAAPESVSGGAGTGTPAADPLATARAVYAVGTTLGYVFPAIIGTLAVTGDLRHRTIVPTLLADPSRTRLLVAKHLGALPVGIAYGLVGSLAALGAGAALITLGGGDPMLGHPEVWRTVALSTVALTLWTLVGVGVGSAISNQVAALVVLLAFTQFVEPIARTGLTAGLGAAGTRIAQFLPGAAGDALAEGSIYSLMAPGTLAPWWQGALVLLGYAVILTVVGRLTTFRRDID
>NZ_CP049862.1|WP_166414364.1|2323298_2324240_+|ATP-binding-cassette-domain-containing-protein
MTISDSPPGTAARLSVRGLTKRFGTVHAVEDLTFDVTPGRVTGFLGPNGAGKTTTLRMLVGLATPTAGSATIGGRRYSELTDPARTIGVALEASTFHPGRTARAHLRMFAPAAGADAARVEQLLDLVGLTPDADRRVGGYSTGMRQRLALATALLGDPEILVLDEPTNGLDPAGIAWLRSFMRNFAASGRTVLVSSHILSEVQHSVDDVVIVAHGRLVHTSSLTELAARAVRTVTVASPDPAALAAVVAQRGWASEPADATSPGALRLRDVHAAEVGTAAFAAGVELHLLSEDSPGLEDVFLRLTGQTTEVAA
>NZ_CP049862.1|WP_166414363.1|2322152_2323256_+|HAMP-domain-containing-protein
MPSPGRHGRVPRPHLPDVRPLDLLRSIRTKLGVLVIATNALAALITWMGLRMHLGPTRTFPLALIVSIIVTAILARGMTSPLREMTAAARAMAGGDYSRRVRATSRDEVGQLAVAFNQMADDLATGDQQRRDLIANVSHELRTPVAALRAQLENIVDGVTPATPATLGTALTQTERLSRLVTYLLDLSRIEAGAADLTVTTVHVADFLDAVVDEVEMVEAGKNLVFEVDVTPAELTLPADPDRLSQIFVNLLHNAIRHAPHGSTVRVAAMRRGDRVVIDVADEGPGIAAADRSRIFERFVHGATPQATASAGTSGGTGIGLAIVRWAVALHDGDIEVVDSEQGATFRVSLPAPRLRGLRVPGRDAGT
>NZ_CP049862.1|WP_166414362.1|2321403_2322150_+|response-regulator-transcription-factor
MSSNAASTGAARGTTILVVEDESTIATAIAQRLTAEGWRVEVARDGLAGVAAASRVLPDAVVLDVMLPGIDGLEVCRRIQAERPVPILMLTARDDETDMLIGLGVGADDYMTKPFSMRELVARLKALLRRVDRAQQAATSPVGEPPIIAGDVTIDRDQRRVHRGGEEIHLTPTEFELLVMLASSPRTVLTRERLLAEVWDWVDASGTRTVDSHIKAVRRKLGAELIRTVHGVGYAFEPPVDGDEGAKG
>NZ_CP049862.1|WP_166415321.1|2319906_2321241_-|HlyC/CorC-family-transporter
MLADWLLVAFGVLLTAGTAVFVASEFALVTIDPAGLESEIAQRSGPGGPDRRTRSVLAALRSLSTELSSSQVGITVTTILLGYTAQPALQRLLVHGFGLTGWAASIVSVVATVTALVLVNLFSMLAGELIPKNFALSAPLATARLVVPVQRVFTRAMHPLITGLNGSANALLRRLGVEPREELSGARSAPELLSLVRRSAQQGTLEASTALLLKNSLELEQLDASDVMTDRTRLVVLTREDSAQRVVELSRSTGHSRFPVIDGSRDEIVGLVHVRRAVGVPRERRAEVPAAALMVEAPTVPETARLGPLLVTLRGLGLQMAVVLDEYGGTAGVVTLEDVVEELVGDVADEHDVRRAGATRQADGAWLLPGLLRPDELTEQTGLVVPDSPVYETLGGLVMSLLGRLPDIGDEVDVDGVHLEVVGMHGRRVARLRATHVAATEEDA
>NZ_CP049862.1|WP_166414361.1|2318860_2319910_-|HlyC/CorC-family-transporter
MSTGTALLVGLALLVGNAFFVGAEFAVLSARRSAIEPLAEAGNRRARTVLWAMEHVSLMLACAQLGVTVCSIGLGMVAEPAIAHALEDPLAALRVPAALVHPVAFTIALAIVVYLHVVLGEMVPKNLAVAGPDAAVMWFGPPLVWLGRAVRPLIVVLNRLANLFVRLGGVEPQDEVASAFTAEQVHSIVEVSRQEGVLDDEQGLLAGSLEFSERVAREVMVPTDALTALVAGATPDDVEHAVTRTGFSRFPLVATEGGPVTGYLHLKDVLYAGESDHDVPVPTWRVRSLATVGPEDEVEEVLAAMQRDGAHLALVVDEGRQTGVVFLEDILEELVGEVRDAMQREADRP
>NZ_CP049862.1|WP_166414360.1|2317089_2318538_-|hypothetical-protein
MSTSSKVEAPAPETRRSRREAALLDARAATAPVSSGAPTTGSATSAPVPVVRPHATAAVTSPYGTLGRPSAHVVVPDLEPDEAPVRATAQSGAASPARAAARPVAGRPHELLGRPVPATSWTPVPQPSIARGAELADAAVAARAALRSSGVTPARPSAVTDTGPVPRTVPAPVAAAARPAAAPAVRTVAPARVTPAEPVVASSAAPADVPTSVEAPTAPPAPAAAPSRQRTRRESVADERRRAGRATPRTAPRRPSGTRAARAGVLAALAIATVAVPVSQGIGQTGDEAVVRDYAEGRATYDVLMSPRGLSDNAVIVADTLAGRDVDLASRSEARPAIAGCDGTVVVPKTSNGRLSGEQLCNLPQQGHQLQPAAALAFAELNAQFVARFNTPICISDSYRSLSGQYSVAASRGAYAARPGTSQHGLGLALDLCSGTYRDSAKWSWLKANAPVYGFDNPAWARRGGSGMYEPWHWEFFSLVDY
>NZ_CP049862.1|WP_166414359.1|2314208_2316956_+|bifunctional-acetaldehyde-CoA/alcohol-dehydrogenase
MTTTAGPGTTSPVAQAIDALVTRGQKALDAFMLLNQEQVDHIVKKASVAALSQHGELAVLAVEETGRGVFEDKAVKNIFACEHVTNSMLKMRTVGIVGEDEITGITEIAEPVGVICGVTPVTNPTSTTIFKALIALKTRNPIVFGFHPSAQASSVAAAKVVRDAAIEAGAPADCVQWVEQPSLEATSTLMNHPGVALILATGGNAMVRAAYSCGKPALGVGAGNVPAFIERSAKLKRAVNDVVLSKAFDNGMICASEQAAILDAPIYDDAMAEFAKLHAYRATPAEKAMLEEFIFGVTAGGENCGGAKLNPAVVGQSPQWIAEKAGFTVPEDTSIILAEVTEVGPNEPLTREKLCPVLAVLRAESAEEGIRLSEQMVEFDGLGHSGSIHSEDQAIIREFGSRIKAVRIITNAPSSLGGIGDIYNAFIPSLTLGCGSYGHNSVSNNVSAVNLVNIKRIGRRNNNLQWFKVPAKTYFEPNAIRYLADMRGISRVTIVTDSTMTKLGFVDKILDVLNRRGERIALQIIDDVMPEPTVDFVQKGAALMRHFNPDTIIALGGGSPMDAAKVMWLLYEHPEIEFADMKEKFFDVRKRAFKFPDLGEKASLVCIPTTSGTGSEMTPFAVISDPAKGKKYPLADYALTPTVAIVDPALTAMMPSFLVADSGFDALTHATEAYVSVYANDYTDGLCLHAIKLIFENIADSVKGGPGATDERTVKAREKMHNASTISGMAFGNAFLGIVHAMAHVTGGTFKLVHGRTNATYLPHVIRYNGTVPTKLTSWPKYEHYVAPERFQEIAKHLGLPASTPEEGVESYARAVEELREQVGIPASFQLQGVDEELFISKLDELAMGAYEDQCAPANPRMPMLDDMKILMEAAYYGTSFAEVKASRKAVGAAAVEAGAEPAEAPKARKAARKR
>NZ_CP049862.1|WP_166414358.1|2312705_2314046_+|APC-family-permease
MTSAPLARRLTLGDAVTLGLGSMLGAGVFAALAPAAGLAGRWLLVALGIAALVATANALSTAQLAAQHPVAGGAYAYGRARLGPWWGFVAGWGFVVGKTASCAAMALTLGAYAWPGHERVVALVALALLVAIDVAGVTRTARATRALLVVTLLALGTLVIVVAVAAATGTLAVPDILGSVDAAGAGAPTGTMLDLQAAPDLTGILGAAGLLFFALAGYARVATLGEEVRDPARTIPRAVAIALVGAVAVVALVAAAALAALGPAALAASVAPLADTARAAGAPWLVPVVGVAAVTASGGALLALLAGVGRTTFAMAREGDLPRALAHVGTRWRTPTTATLLVGAAVAVLVWTTDLRGVLGASSAGVLLYYGVANAAAWTQPRGERIVPRWVPALGLAGCLALVATLPRDALAVAGAVLVAGAVGRVLAQAVGRRGEPRGDADDAPL
>NZ_CP049862.1|WP_166414357.1|2312118_2312601_+|hypothetical-protein
MWRVAAPSATRDAWTDYVWDGKPDLGPHLLPDGRDILDEIREGRAGELPFPVQARIYQGKRINDMLWTGGLGMIASTALVAVLNDLGVAGYATYDLDVRNRDGSPLPGFVGFRTTSDTLDTDITDLGRGGSYIFYTTDRVANALRDTKLKLDITPVTPRG
>NZ_CP049862.1|WP_166414367.1|2329485_2330466_+|aldo/keto-reductase
MQTKRWSDGQQVSAIGLGTWQLGADWGDVEEKDAHAVLDAALEAGVTFFDTADVYGDGRSEQIIGSFLRARPDAAIFVATKAGRRMPQVHENYSLANLRAWTDRSRRNLGLDTLPLVQLHCPPTSVYTDDEVFDALGTLVDEGAIASWGVSVEKRVEALRALERPGLASIQIVLNAFRLAPFDDVVPTAVDRGVAIIARVPLASGLLANRYTPTTTFAADDHRTFNRNGEAFDVGETFAGVDFATGVAAAAELASHGPDDLTAAQAALAWLAQHDAVTTVIPGARTPEQARANAAAGAAAPLPAAYDEAVHRIYDRDVRASVHERW
>NZ_CP049862.1|WP_166415322.1|2330553_2331141_+|lysophospholipase
MRIVVVGDELAAGVGDPRALGWVGRVVARTTEVETEHYVLAAPGETSTALSARWEREVEPRLTTDPDVDQRLVVALGRHDLTAGLSVARSRLNLANTLDVAEARHLRTLVVGPPPGSRADDDRLADLSRAYGDVAQRRRVPFVETFTPLVNHDQWHADLAGRGDDLPQQAGYGLMAWLVLHSGWHRWLGLADPDA
>NZ_CP049862.1|WP_166414368.1|2331210_2332296_-|PilT/PilU-family-type-4a-pilus-ATPase
MNATPQSVIPLLHAVVKAEASDLHVKVGSAPRVRVDGRLRRLQVPVLTPMDTDHMLSQVLPADLVDQFERTHEADFAYSVAGVGRFRVNAYQARGTTAMVFRLVGMGTSSLAELGVPGIVGDLALEPRGLVLVTGPTGAGKTTTLAAMVDLINTHREVNIITIEDPIEVLHEDKRAIISQREVRQDTKDFSTALRAAMRQDPDVILVGEMRDIETVRAALQAAETGHLVLSTLHTIDAQETVNRIIDFFPPYEQLQIRTALSQMLRGIVSQRLVRTVDDNRCPSVEVLVNTGRTAEAIVNPLDNPPLADLIADGGYYKMQTFDQHLCELVVSGRITYDEAIVSASNPQDLTLSLRGMGVEV
>NZ_CP049862.1|WP_166414369.1|2332723_2334022_-|citrate-synthase
MTQNAQTGVSLTVGQVTQDLPVVPATEGNDGIVVSSLLGTTGKVTLDPGFTNTASCESGITYIDGGEGILRYRGYPIDQLAEGSTFLEVAYLLIHGELPSADELEAFVTRVNRHTLVHEDFRTFMGTFPRNAHPMAVMASAINALSTFYPESLDPFDDETVELASVLLLAKTRTITSYVHRRSVGEPLLYPDYSRGYVDDFLRMSFAQPYMPYEADPIVVDALDTLLVLHADHEQNCSTSTVRMVGSAHANLYASVSAGINALSGPLHGGANEAVLTMLTDLKKSGDDVDTYMSRVKNKEAGVRLMGFGHRVYKNYDPRAAIVKKKAYAVLDALGARDELLDIALRLEEIALNEDYFIERKLYPNVDFYTGLIYKAMGFSPAMFTPLFALGRMPGWIAQWREMMKDPTTKIGRPRQVYTGATERAYVPVENR
>NZ_CP049862.1|WP_166414370.1|2334279_2335416_-|succinyldiaminopimelate-transaminase
MGLSSLAGLAFPWDLLEPAKARAAAHPDGIVDLSVGTPVDATPDVVRRALESASDAHGYPLTAGTPALRAAVAGWFARRRGVTVAPDATLPTVGSKELVGLLPSMLGLGAGDTVVHPAVAYPTYDVGARLAGATSLATDDVRDWDGREGVRLVWVNSPGNPHGRVADVAELRAVVEAARRTGAVVVSDECYAELGWGDGPHDPQTVPSLLDPRVCGDDHTNLLVTYSLSKQSSMAGYRAAFVAGDPALVGALLGLRKQLGLIVPGPVQAAMVAALDDDEHVAVQRESYRARRDLLGAALTDAGFVIDHSEAGLYLWVRPAGERVDCWATVDRLAQIGLLVAPGAFYGAAGEGHVRVALTVTDERAEAAANRLSTLVDA
>NZ_CP049862.1|WP_166414371.1|2335738_2337466_+|nitrite/sulfite-reductase
MTTTAPGQPEAAPRASRGVARPSRSTRPQGQWKVDGTEPLNANEVIKQKDDGLNVRERIETIYAAGGFESITKEDLHGRFRWWGLYTQRRPGIDGGRTASLEPHELDDEFFMMRVRSDGGALTTEQLRVIGEISVEFGRSTADITDRHNIQLHWIDVRDVPEIWRRLEDVGLSTTEACGDVPRVILGSPVAGVAKDEIIDPTPVIREIVDRYIGDPTFSNLPRKYKTAITGHPSLDVLHEINDLGLVGVVHPDLGPGYDVWVGGGLSAQPRLAERLGAFVTEEQVPDVWVGVTSIFRDYGFRRLRNKARLKFLLADWGAEKFREILETEYLGYRLADGPAPAPAPRSGDHVGVHEQKDGRFYVGAAPYVGRVSGETLLEVARLAEAAGSGRIRLTPQQKLLVLDVPAEHVPALVDGLRATGLEAEPSAWRRSTIACTGIEFCKLAIVETKGLARETIQALETRLDRGERRPITINVNGCPNACARTQIGDIGLKGQIVTTADGEQVPGFQVHLGGGLSGHRRDEGGLGRTVRGLKVTADDVASYVDRVVSRYDAEHEGDETFADWALRVDDEVLA
>NZ_CP049862.1|WP_166414372.1|2337462_2338368_+|phosphoadenylyl-sulfate-reductase
MSAVDLPGPFGLALPGLAGAGTGQGVVGQGRAGDLAAFGAAGRARAAEHERARVAHAAARAARDARRRSDDELKRLAAEGAALLSPADGPEASADEISAWAAETFGDLLTVACSMADLVLPHVVAQRAPWVDVLFLETGYHFPETIGTRDAAAATMPITVVDVAARQSVAEQDAQYGPRLHERDPGLCCALRKVAPLQASLGGYEAWVTGVRRDEAPTRTGTPLVSWDEKNRLVKINPLAAWSFDDLLGYATQHKVLLNPLLDDGYPSIGCAPCTRRVAPGEDPRSGRWAGLDKTECGLHA
>NZ_CP049862.1|WP_166414373.1|2338364_2339309_+|sulfate-adenylyltransferase-subunit-CysD
MTTTTDAPAAQAAPYTLSHLDQLESEAIHIIREVVAEFERPALLFSGGKDSVVMLHLAAKAFWPAPVPFPVVHVDTGHNFPEVLAYRDAEVERLGLRLVVASVQDYLDDGRLQERADGTRNPLQTQPLLDAISGGRFDAVFGGGRRDEEKARAKERVLSLRDEFGQWDPRNQRPELWNLYNGRHRPGEHVRAFPLSNWTELDVWRYIERENIALPGLYYAHEREVFDRDGMLLAVGPYSAPRSDAEAASVRTEVVRYRTVGDMSCTGAVSSDAVTVADVIAEVATTRITERGATRADDRISEAAMEDRKKEGYF
>NZ_CP049862.1|WP_166414374.1|2339364_2340696_+|sulfate-adenylyltransferase
MSTATLPASATLLRLATAGSVDDGKSTLVGRLLFDSKSVLADQLDAVERVSRDRGLEGADLALLTDGLRAEREQGITIDVAYRYFATARRAFVLADCPGHVQYTRNTVTGASTADAVVLLIDARKGLLEQTRRHLAVASLLRVPHVVVAVNKIDLVDYSAERYAELAAEIRATAADLGVPAIHTVPVSALVGDNVVDRSAATPWYDGPSLLELLEDLPVGEDVAAQHLRFPVQVVLRPQGAARDPLHVDYRGYAGQIAEGVVRPGDEVVVLPSGKRTLVEAIDTADGPLAEAFAGQSVTLRLTDEIDIARGDQIVAATDVPALTQDVTATLAWLGENPLRPGQRVLVKHTTKVVQAIVRDVVGRLDLDAAHLVPGDALELNDIGRVQLRLAAPIPAEEYVDHRRTGAFCVIDPADGRTLAAGMVGDALAAARFPGDRPVDFAI
>NZ_CP049862.1|WP_166414375.1|2341023_2342307_+|uroporphyrinogen-III-C-methyltransferase
MDTSTTDPAYPLTLRVAGRRCVVVGAGPVGTRRALALVRAGAVVTVVAPVASADVRGAAARGELTWEQRPYATGDLADAWVAHTATGVRAIDEAVSADAEAARVWLGRADDRTRSSLWSPAVARIDDITVTVGAGGDPRRAMELRDKIAGALREGTISAPRHRAAASTTPSPLSAVPPAEPVPAPPGVGSVALVGGGPGDPGLLTLRAAEMLAQADVVVLDRLAPRAALEHARDDVEVVDVGKTAGTHPVPQEAINALLVERALAGRRVVRLKGGDPYVFGRGGEELDACAAAGVPVEVVPGVTSAISVLAAAGIPVTHRGLSRGFTVLTGHDDLGTVPDAADHTLVLLMGLGRLATTAAELVARGRDPRTPAAVLEDGFGPRARTTLGTLATIGEIAVAAGVRAPAITVVGPVVTRAPGWAHTSDG

Crispr_ID: NZ_CP049862_10

• CRISPR_ID: NZ_CP049862_10
• CRISPR_location: 3041396-3041493
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP049862_10

Consensus_repeat	Method
TCGATAGCCGATCCGTGCACCTCACA	CRISPRCasFinder

spacers of NZ_CP049862_10

>10.1|3041422|46|NZ_CP049862|CRISPRCasFinder
CGTACGGATCCGCTATCCGGCGACTGCAGCACGCCCCACACAGCTG

CRISPR arrays and Neighbor proteins around NZ_CP049862_10

CRISPR arrays

The CRISPR arrays of NZ_CP049862_10

>merge|NZ_CP049862|10|3041396-3041493|CRISPRCasFinder
TCGATAGCCGATCCGTGCACCTCACACGTACGGATCCGCTATCCGGCGACTGCAGCACGCCCCACACAGCTGTCGATAGCCCATCCGTGCACCTCACA

>NZ_CP049862|10|10|3041396-3041493|CRISPRCasFinder
TCGATAGCCGATCCGTGCACCTCACA	CGTACGGATCCGCTATCCGGCGACTGCAGCACGCCCCACACAGCTG
TCGATAGCCCATCCGTGCACCTCACA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP049862.1|WP_166414900.1|3048410_3048995_-|orotate-phosphoribosyltransferase	unknown	unknown	gnl|CDD|234771
NZ_CP049862.1|WP_166414889.1|3030680_3031964_-|adenylosuccinate-synthase	unknown	unknown	gnl|CDD|234904
NZ_CP049862.1|WP_166414901.1|3049132_3049888_-|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|223377
NZ_CP049862.1|WP_166414896.1|3039694_3041356_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|223562
NZ_CP049862.1|WP_166414898.1|3046185_3047658_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166414894.1|3037665_3038325_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP049862.1|WP_166414899.1|3047654_3048386_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|224054
NZ_CP049862.1|WP_166415383.1|3032118_3032583_-|DUF3151-domain-containing-protein	unknown	unknown	gnl|CDD|378646
NZ_CP049862.1|WP_166414903.1|3050818_3051613_+|hypothetical-protein	unknown	unknown	gnl|CDD|379388
NZ_CP049862.1|WP_166414902.1|3050027_3050822_+|exodeoxyribonuclease-III	unknown	unknown	gnl|CDD|197320
NZ_CP049862.1|WP_166414904.1|3052015_3052852_+|C40-family-peptidase	unknown	unknown	gnl|CDD|366353
NZ_CP049862.1|WP_166414895.1|3038522_3039542_-|class-II-fructose-bisphosphate-aldolase	unknown	unknown	gnl|CDD|236406
NZ_CP049862.1|WP_166414897.1|3043322_3046031_-|hypothetical-protein	unknown	unknown	gnl|CDD|367875
NZ_CP049862.1|WP_166414891.1|3034475_3034811_+|STAS-domain-containing-protein	unknown	unknown	gnl|CDD|132914
NZ_CP049862.1|WP_166414890.1|3032611_3034345_+|sodium:proton-antiporter	unknown	unknown	gnl|CDD|129911
NZ_CP049862.1|WP_166414888.1|3029414_3030581_+|LCP-family-protein	unknown	unknown	gnl|CDD|367673
NZ_CP049862.1|WP_166415385.1|3042486_3043227_+|HAD-family-hydrolase	unknown	unknown	gnl|CDD|319832
NZ_CP049862.1|WP_166415384.1|3041538_3042297_-|RNA-methyltransferase	unknown	unknown	gnl|CDD|349969
NZ_CP049862.1|WP_166414893.1|3037235_3037658_+|STAS-domain-containing-protein	unknown	unknown	gnl|CDD|379202
NZ_CP049862.1|WP_166414892.1|3034846_3037327_-|SpoIIE-family-protein-phosphatase	unknown	unknown	gnl|CDD|369272

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP049862.1|WP_166414889.1|3030680_3031964_-|adenylosuccinate-synthase	gnl|CDD|234904	PRK01117, PRK01117, adenylosuccinate synthetase; Provisional.	0
NZ_CP049862.1|WP_166414901.1|3049132_3049888_-|SDR-family-NAD(P)-dependent-oxidoreductase	gnl|CDD|223377	COG0300, DltE, Short-chain dehydrogenases of various substrate specificities [General function prediction only].	1.35133e-69
NZ_CP049862.1|WP_166414896.1|3039694_3041356_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein	gnl|CDD|223562	COG0488, Uup, ATPase components of ABC transporters with duplicated ATPase domains [General function prediction only].	1.46609e-138
NZ_CP049862.1|WP_166414900.1|3048410_3048995_-|orotate-phosphoribosyltransferase	gnl|CDD|234771	PRK00455, pyrE, orotate phosphoribosyltransferase; Validated.	1.11378e-66
NZ_CP049862.1|WP_166415383.1|3032118_3032583_-|DUF3151-domain-containing-protein	gnl|CDD|378646	pfam11349, DUF3151, Protein of unknown function (DUF3151). This family of proteins with unknown function appears to be restricted to Actinobacteria.	7.03339e-53
NZ_CP049862.1|WP_166414899.1|3047654_3048386_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	2.27862e-34
NZ_CP049862.1|WP_166414903.1|3050818_3051613_+|hypothetical-protein	gnl|CDD|379388	pfam13828, DUF4190, Domain of unknown function (DUF4190). This integral membrane domain is functionally uncharacterized. One of the membrane helices contains two GXXG motifs that are usually associated with dimerization.	3.11193e-05
NZ_CP049862.1|WP_166414902.1|3050027_3050822_+|exodeoxyribonuclease-III	gnl|CDD|197320	cd09086, ExoIII-like_AP-endo, Escherichia coli exonuclease III (ExoIII) and Neisseria meningitides NExo-like subfamily of the ExoIII family purinic/apyrimidinic (AP) endonucleases. This subfamily includes Escherichia coli ExoIII, Neisseria meningitides NExo,and related proteins. These are ExoIII family 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 efficiencies. Many organisms have two AP endonucleases, usually one is the dominant AP endonuclease, the other has weak AP endonuclease activity. For example, Neisseria meningitides Nape and NExo, and exonuclease III (ExoIII) and endonuclease IV (EndoIV) in Escherichia coli. NExo and ExoIII are found in this subfamily. NExo is the non-dominant AP endonuclease. It exhibits strong 3'-5' exonuclease and 3'-deoxyribose phosphodiesterase activities. Escherichia coli ExoIII is an active AP endonuclease, and in addition, it exhibits double strand (ds)-specific 3'-5' exonuclease, exonucleolytic RNase H, 3'-phosphomonoesterase and 3'-phosphodiesterase activities, all catalyzed by a single active site. Class II AP endonucleases have been classified into two families, designated ExoIII and EndoIV, based on their homology to the Escherichia coli enzymes ExoIII and endonuclease IV (EndoIV). This subfamily belongs to the ExoIII family; the EndoIV family belongs to a different superfamily.	1.32662e-121
NZ_CP049862.1|WP_166414904.1|3052015_3052852_+|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.	4.54401e-28
NZ_CP049862.1|WP_166414895.1|3038522_3039542_-|class-II-fructose-bisphosphate-aldolase	gnl|CDD|236406	PRK09197, PRK09197, fructose-bisphosphate aldolase; Provisional.	0
NZ_CP049862.1|WP_166414897.1|3043322_3046031_-|hypothetical-protein	gnl|CDD|367875	pfam04213, HtaA, Htaa. This domain is found in HtaA, a secreted protein implicated in iron acquisition and transport.	8.69528e-42
NZ_CP049862.1|WP_166414891.1|3034475_3034811_+|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.	6.55639e-13
NZ_CP049862.1|WP_166414890.1|3032611_3034345_+|sodium:proton-antiporter	gnl|CDD|129911	TIGR00831, Putative_Na+/H+_exchanger_Rv2287/MT2345/Mb2309., Na+/H+ antiporter, bacterial form. The Monovalent Cation:Proton Antiporter-1 (CPA1) Family (TC 2.A.36) The CPA1 family is a large family of proteins derived from Gram-positive and Gram-negative bacteria, blue green bacteria, yeast, plants and animals. Transporters from eukaryotes have been functionally characterized, and all of these catalyze Na+:H+ exchange. Their primary physiological functions may be in (1) cytoplasmic pH regulation, extruding the H+ generated during metabolism, and (2) salt tolerance (in plants), due to Na+ uptake into vacuoles. This model is specific for the bacterial members of this family. [Transport and binding proteins, Cations and iron carrying compounds].	2.40438e-55
NZ_CP049862.1|WP_166414888.1|3029414_3030581_+|LCP-family-protein	gnl|CDD|367673	pfam03816, LytR_cpsA_psr, Cell envelope-related transcriptional attenuator domain.	2.76625e-41
NZ_CP049862.1|WP_166415385.1|3042486_3043227_+|HAD-family-hydrolase	gnl|CDD|319832	cd07530, HAD_Pase_UmpH-like, UmpH/NagD family phosphatase, similar to Escherichia coli UmpH UMP phosphatase/NagD nucleotide phosphatase and Mycobacterium tuberculosis Rv1692 glycerol 3-phosphate phosphatase. Escherichia coli UmpH/NagD is a ribonucleoside tri-, di-, and monophosphatase with a preference for purines, it shows peak activity with UMP and functions in UMP-degradation. It is also an effective phosphatase with AMP, GMP and CMP. Mycobacterium tuberculosis phosphatase, Rv1692 is a glycerol 3-phosphate phosphatase. Rv1692 is the final enzyme involved in glycerophospholipid recycling/catabolism. This subfamily belongs to the UmpH/NagD phosphatase family, and to the haloacid dehalogenase-like (HAD) hydrolases, a large superfamily of diverse enzymes that catalyze carbon or phosphoryl group transfer reactions on a range of substrates, using an active site aspartate in nucleophilic catalysis. Members of this superfamily include 2-L-haloalkanoic acid dehalogenase, azetidine hydrolase, phosphonoacetaldehyde hydrolase, phosphoserine phosphatase, phosphomannomutase, P-type ATPases and many others. HAD hydrolases are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	9.10029e-120
NZ_CP049862.1|WP_166415384.1|3041538_3042297_-|RNA-methyltransferase	gnl|CDD|349969	cd18096, SpoU-like, SAM-dependent rRNA or tRNA methylase related to SpoU. RNA 2'-O ribose methyltransferase catalyzes the methyltransfer from S-adenosyl-L-methionine (AdoMet) to the 2'-OH group of ribose in tRNA or rRNA. 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.	3.09483e-65
NZ_CP049862.1|WP_166414893.1|3037235_3037658_+|STAS-domain-containing-protein	gnl|CDD|379202	pfam13466, STAS_2, STAS domain. The STAS (after Sulphate Transporter and AntiSigma factor antagonist) domain is found in the C-terminal region of Sulphate transporters and bacterial antisigma factor antagonists. It has been suggested that this domain may have a general NTP binding function.	8.84717e-11
NZ_CP049862.1|WP_166414892.1|3034846_3037327_-|SpoIIE-family-protein-phosphatase	gnl|CDD|369272	pfam07228, SpoIIE, Stage II sporulation protein E (SpoIIE). This family contains a number of bacterial stage II sporulation E proteins (EC:3.1.3.16). These are required for formation of a normal polar septum during sporulation. The N-terminal region is hydrophobic and is expected to contain up to 12 membrane-spanning segments.	1.51496e-36

Protein sequences

>NZ_CP049862.1|WP_166414896.1|3039694_3041356_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein
MTATLVVKGLAAGHADRTLFSGLDLVVAPGDVVGLVGANGAGKSTLLRILAGSDEPAEGAVTLSPPGAVVGHLAQEVERLPDETVGAYLARRTGVADAQSALDATTDALAAGTPGSDDAYADALERWLALGAADLEDRTGAVLADLGLDVDVDHPVVGLSGGQAARLGLAALLLSRFDVLLLDEPTNDLDLDGLARLERFVAEQRAGVVVVSHDREFLARCVTRVVELDLAQQQVGVYAGGYEAYLEERATARRHAREAYEEYADRRGALESRAQMQRQWLAKGVRDAVKKSTDPDKHIKHAHREGSEKQAAKARQTARMIERLEEVAEPRKEWELRYSIAAAPRSSSVVATLRGAVVHRGETPAGPAFTLGPVDLQLDAGDRVAITGANGSGKTTLLAALLGRAELAAGAASLGSSVAIGEVDQARAALAAEPGQGLLDAFGAQVPDMAPAEARTLLAKFGLRADHVLRPLASLSPGERTRASLALLQARGVNLLVLDEPTNHLDLPAIEQLEEALEEYTGTFLLVTHDRRMLDAVRVTRRWTLDAGRLTES
>NZ_CP049862.1|WP_166414895.1|3038522_3039542_-|class-II-fructose-bisphosphate-aldolase
MAIATPEVYAEMIDRAKAGKFAYPAVNITSSQTVTAAIQGFAEAESDGIIQVSVGGAEYASGSTIKDRVAGSLALAAYATEVAKGYGVTIALHTDHCTAANLDSWVRPLLAIEAEQVKAGKNPTFQSHMFDGSTVPLAENLVIAEELLALSQAARTILEIEVGVVGGEEDGHEAEINEKLYTTVEDGLATVKALGTGEKGRYLTALTFGNVHGVYKSGAVKLRPALLKEIQDGVAAVIGKENPFDLVFHGGSGSTAAEIAEAVDNGVIKMNVDTDTQYAFSRPVADHFFRNYDGVLKVDGEVGNKKAYDPRAWGKLAEAGMAARIVEAAQQLRSAGQKL
>NZ_CP049862.1|WP_166414894.1|3037665_3038325_-|hypothetical-protein
MTLQHIRPRAGMPALALLTLGALAACGSAPDDAPGGGARATETVVMAADYPVYLTARELDEVADTVVRGIVRSSETGFERLVLDTSSDDPQLNPLAGLSEDEIDAYLARNDGYVATTHSLEVTEVLQGDVGVGDTVTVQQIGGTHDGVSYVVLGIEQLSVGREYLLVTTAREGGRLELVSSGQSVFTVGADGALAPLATNPGGYVLRGTLAEAREVFPG
>NZ_CP049862.1|WP_166414893.1|3037235_3037658_+|STAS-domain-containing-protein
MRDENAAEETAPAQDEPGTLHVLVGANRTRIVLSGEIDANLAQEFSDAMADAQEIDLPVEVDAHHVTFMDSSGVAFLARLAAQTPQKVRVLRAPQTMRFLLEVTRVGELVEILDEDPGFEFAPIDEFTIERLPGQINPPR
>NZ_CP049862.1|WP_166414892.1|3034846_3037327_-|SpoIIE-family-protein-phosphatase
MRVRFAPTRTWRVPGSSWAGAVSSAAFSSRTACSSRPRVGGPASNPRTSRSLRRGLERSGGHRVLSPQDGPAGPGEAAPGQVPCEDRTTGTGRSNDVGGREGVPGNAVPAAAPVQAPVPDDALDLLPGLAAQHVGVGLTTLGVRDGVVRMLWVNDVFSRITGYAAHEVVGLEPRLFYSDQWSEVGVASLATEVRAGRTASITLPFRRPDGASVWLALSLTAVPADAVASVVPTEDEADGGPAEMWIASFSDVTGTVERNVHLRDAMRAERRARLHLALLSRVSDLLSEPDPDEALTQVTALLAPALVQWAGAFLVEGGLRLVGHDPGRADGLRRDAARRRTLRRVSPGDPTGAYEIDRVLGGLQSEAILDLTLVHPDESAAALVQGQVLAAEPGLALLSPRVRVVGVLGSRSVLALLVHAVSESGGVPQLADELEQVLGVVVRRVGLALDNARLYAREHELAETMQRSLLPRQVEIDGLDLWTYYAPSVAHAQVGGDWYDVLEVAPGVAGVVVGDVVGHDVEAAALMGQLRSVVRAYAFEGGSPASVLDRTDQLMRGMRAPRAASAVYGTLMPRVGSPGTWVFEYARAGHLPAVLVRDGQATQLAQGAGALIGFGRRARTGGRAVLVPGDTLVLYTDGLIERRARPLRAGLEALLAAAARTQAQDAAGIGEELLAALADSPEDDVAVVVVRVPQEGAPTTGTAAGPRSRRWSMPSDPAAIARSRHAVLRTCEAWGIAEVADAELVVSELVANAVLHGWGTVELRLFDTGDGLRIEVEDANPAPPVKLDGHAHGVGGYGVQIVDRLADWGWRAANDGKIVWARLRAR
>NZ_CP049862.1|WP_166414891.1|3034475_3034811_+|STAS-domain-containing-protein
MIQIATSPATTTLTITGDLDLAERDQFPEITARVVGLRRQLLVLDMCGVTFMDSTGAAFLIALADAGRRRGGATVLRGCDERDLFVLEVCGALDLFRVDAEHACSHDEASA
>NZ_CP049862.1|WP_166414890.1|3032611_3034345_+|sodium:proton-antiporter
MELALLGVVAVLVIVAVAGVAPRIGVAAPVILVLLGTIGGYLPGVEPVVVDPEIVLMVVLPPILYAAAVNVPLMDFRRNFRAITGLSVVLVVLSAVVVGLVLRLLLPDLSFAAAIALGAVVAPPDAVAATAVGKKLGLPHRLVTVLEGEGLVNDATALVLLRSAVAATAATAASVEVADVAVDFVRAVAIALVIGAAVGLAAVFVRGRMSDPVLSTAISFAVPFVAFIPAEHLHASGVLAVVVAGLLTGHLAPKHLSPADRISERTNWRTAQMLLENGVFLLVGLELHGIVDQVADDDLSVGQAVAIGVLVAAVLTVVRAGFVVPLVASLRRERRRAVVRAAHLDSVLSRIEEARTVLPPEILEDPRFRERGRRVTRKIRRRRADLGSLQADGLGWRGGAVLAWSGMRGVVTVAAAQTLPADLPYRPQLVLIALTVAIVTLVVQGGTLPWVIRIVGVQGTDEDVEREQLATLVGEITSAGVACLENPSLRRSDGSEFPPETLEGVRDAIRRTASLLTVHGAEDGQGPASDHHALRRRAIEAERAALADARTSGAHPSHVVDHVEHLLDLEEARLDLA
>NZ_CP049862.1|WP_166415383.1|3032118_3032583_-|DUF3151-domain-containing-protein
MRPWHDDAMTSPTGPRLERIELGRIVTHLPADGPDRAAREMLAAGSPAREAARAVPSSSLAWALLAEASLAEDAVASYAYARTGYHRGLDALRRAGWRGTGEVPVDHEPNQGFLRALLALARAAAAIGEDDEAERCAGFLGDCGTDAAAVDATR
>NZ_CP049862.1|WP_166414889.1|3030680_3031964_-|adenylosuccinate-synthase
MPAIVVVGAQWGDEGKGKATDQLGSQVDYVVKFNGGNNAGHTVVVGSEKYALHLLPSGILSPGVTPVIGNGVVVDIEVLFEELDDLIARGVDVSRLLVSSAAHVIAPFHRTLDKVSERFLGKRRIGTTGRGIGPAYADKINRVGIRVQDLFDEKILRQKIEGSLDQKNHLLVKVYNRRAITVDETVAELLGYAERLRPMVADTSLVLNQALDAGKTVLFEGGQATMLDVDHGTYPFVTSSNATAGGVCTGSGIGPTRIDRVVGVIKAYTTRVGEGPFPTELLDEMGEYLRTTGGEYGVTTGRPRRCGWYDAVIARYSARVNGLTDFALTKLDVLTGLEQIPVCVAYDVDGVRFDEMPLDQSDFHHAKPILEYFPGWTEDITAARTFEDLPANAQAYVLALEGMSGSRMSVIGVGPDREQTIVRHALV
>NZ_CP049862.1|WP_166414888.1|3029414_3030581_+|LCP-family-protein
MPASTRLVRHARLRRDHRALRATGLTLAGVLAFGGTAAAMVNHDLQRSLNVQDIDGLLGTDRPTIVEDPSDPYAGKQLNILVMGTDMRDAENEAIAGKADTMASDTTMVVHISGDRKHVEVVSIPRDSMVALPACTTGDGGTSYASDYAMFNSAFAIGAGSTQNLETAAACTVKAVEQLTGVRITSHIVLKMTGVVDVVDALGGVEVDLPEPVVGFKKWSNINLPAGKQTLDGRTSIEFLRVRKGTGMGLNQGSDLTRITRQQFFLDAMVKQVLSQNLVTDSPKLYGVVKSVLAAISTSPDLGTTSALAGLAFSLKDTPSKNIVFTELPLGTDPRDKNRVVWLPEAEEIWQRIIHDEPAPQPTDEPTDGASAGSKDGAKDKATTGAQG
>NZ_CP049862.1|WP_166415384.1|3041538_3042297_-|RNA-methyltransferase
MPDDARADASPDETRPDVPVVGAPAADGPDATSDVERTLPGEEREVGVGPWPGGEAAWPRLPGGALDPRFDPELLRDGDRRNVVDAYRYWSLEAVVADLDTRRHPLHVAIENWHHDLNIGSVVRTANAFLVAEVHVVGRRRWNRRGAMVTDRYQHLRHHASVADLLAWARAEGLPVVGIDNVPGSVPVETAELPERCLMLLGQEGAGLTPEALAACSTVLHIAQFGSTRSLNAGAAAAIAMHTWVRQHATLP
>NZ_CP049862.1|WP_166415385.1|3042486_3043227_+|HAD-family-hydrolase
MDGVLVHENEALPGAAEFIRTLRDKDRPFLVLTNNSIFTDRDLRARLAASGIDVPIESIWTSALATATFLRTQSPGGSAYVIGEAGLTTALYEAGYTLTDKDPDYVVLGETRTYSFEAITTAVRLILGGARFIATNPDVTGPSGDGPLPATGAVAAMITKATGREPYFVGKPNPMMFRSALNRIDAHSRVTAMIGDRMDTDIVAGIEAGLETFLVLTGSTSAEEVETYPFRPSRVVAGIGDLIPLI
>NZ_CP049862.1|WP_166414897.1|3043322_3046031_-|hypothetical-protein
MLLPARARSAVAALAALAVALTAAVVGLAAPASAEPSVEPAGPTVTVSKTTGLTDGETVTVRGSGFLPAGAATTGTRPPLAGKFTGVYVAFGRFADVWKPSANVASDARVAGDTKWAVLAEDMAVIGGAARGAIELRADGTFETELTLAQSQKLQEATGNWGVYTYPGGGAKHEPFETYTPLTFADPVVAPTVTVSKTTGLTDGETVTVRGSGFLPAGAATTGTRPPLAGKFTGVYVAFGRFADVWKPSANVASDARVAGDTKWAVLAEDMAVIGGAARGAIELRADGTFETELTLAQSQKLQEATGNWGVYTYPGGGAKHEPFETYTPLTFGTSPEPTPTPTSEPTPTSEPTPTPTPEPTPNPTPTTDPVCVADDSVASSTLAWGVKKSFVDYLTGPIAGGKVARTGVALEDGRFVWSKGTGTYAAGKGTVAFPGSLRFTGHHDELDMTFTDVRLVVVSATKAEIRIDADIKAYLGNPAQVLDDVVIGTVDLRGAVSTSGETTRIVNAPVTLAATGVPAFAGFYEAGDALEPVSATLTVTKVCDEPGTDGPGTGEPGTGEPTEAPAPAVSLGGDVEGTDVARGGTVSFTTTGLPSRASTSAEVHSDPVSLGSRRASATGSVTYTFKVPADFPKGKHTFVLTAAGVEGTVTRTFSVVGASEPTTTPSDGSTAEPSDTATTSDAPSCTARVVSGATLSWSIKDSFVSYIEGSIAQGSIATSGARRSGSTFTWSGGSGTFNATDVRGTARFSGSVTTTGHDGKLEVRFANPHVVVTGSTGQLVLDVSGVTLEGEDFAYTGITFATLALAGHGGTSGGKVAYSGVPATLTAAGAKAFSGFYTTGEQLAPVSFTLPLGAETDCTPDSGTLPTTGAEAAGLGGAAAALVVLGLGLVALQRRRARLEV
>NZ_CP049862.1|WP_166414898.1|3046185_3047658_-|hypothetical-protein
MIATDATGVRGALAVWAARAPRALGDLAYLVYIVALSALILLGPGVRAAWLLATGAGGRAVLVDPSVPSTWAAATALVWLAALVVGRERGPASRPPFLAAVLGDADVPRTRSFGGPVLRATLALVAVGALVPALPVIALVDLGVATPGDAGLVVAAGAVAGLVTAGAWLAGQVLPGRAFAAVVGVLGAGAALAVAGAWTWAPWALVGATWPGASVHRGGTVVGVVLALGMVAPLLRGLERLATSRIVGQAVRAQRAQALVDAMDLQASGEVYRALPSAGRRLTAVGHVSGPAAVVVGDVVGSLRTPARLLGGVVALVVAGAVVGAELPGTTLSVGPVLAAILAYAGVSVLCDGLRHAAALGEGSGQYGLSRPALRGLHAVWPAFAGVGLAVMGAALAGAPVGLAAALSGVVVAVRLADVLKGVMPVEMLVPIVTPMGDMSAAGRAVWLADGPLLVLAAGVAGGFAADGRGGLGLVAALVAAVLGRRWLRR
>NZ_CP049862.1|WP_166414899.1|3047654_3048386_-|ATP-binding-cassette-domain-containing-protein
MTGAGVAVALDAVSVVLDGTTLLAPTSVAVPAGGTLVVRGPNGSGKSTLLRVVAGVRTPTTGTATVDGRAPDPRRRAFRRLVAGTVESPVPARDLTLAEHVALVATTWGTPVRAARTLAAELLERLGVGALAARFPHELSSGQTQLAALAVVLARPSALLLLDEPEQRLDADRVATVAELLAERRAAGTTLLVATHSDALEAALGGPTLRLVPAGPGAADDVPDDDVLEDDTPDASADGHPDA
>NZ_CP049862.1|WP_166414900.1|3048410_3048995_-|orotate-phosphoribosyltransferase
MTDYDAVLSPSPREQLRDLVKELAVVHGKVTLASGKEADYYVDLRRVTLHHRAAPLVGHVLLDALEEAGLGPAEIDAVGGLTLGADPVAGALLHAAASRGQDLDAFVVRKEGKAHGMQRRIEGPDVAGRKVVAVEDTSTTGGSVLTAVEALREAGADVVGVAVIVDRNTGAREKIEAEGLSYLYLYGLDDLGLA
>NZ_CP049862.1|WP_166414901.1|3049132_3049888_-|SDR-family-NAD(P)-dependent-oxidoreductase
MGTALVTGASAGLGEEFAWQLATARHDLVLVARDAARLEALAVRLRAAAGVHVEVLPADLSVREDVARVAARLEADERPVGLLVNNAGYTVHQRFTRSDLDAQDALLEVMVRSVQALSYAAARAMKDRGRGAILNVSSVAAHTVSGTYSAAKAWVLAFTEGLAVELGGTGVTATALCPGLTRTEFHERAGFRRLGPGWFWLDRADVVRVALADVRRGAVVSVPSARYRVATTVARHLPRGAMRTLTKRAGL
>NZ_CP049862.1|WP_166414902.1|3050027_3050822_+|exodeoxyribonuclease-III
MRIATWNINSIRARADRALAFLEREDVDVLALQETKCKDAQFPREAFEAAGYEIATFGFSQWNGVAILSRVGLEDVTAGFDGQPEFGETPAVEARALGATCGGVRVWSLYVPHGRALDNPHYPYKLAWLARLRELAGTWGDAGEKVALVGDWNVVPLDSDVWDVAAFEGQTHVSEPEREAFRAFAEAGYTEVSRQFLPDEHRYTYWDYQQLRFPRNEGMRIDFAYTSPALTPLVTDVRIDRDERRGKGASDHVPVIVDVDTSTS
>NZ_CP049862.1|WP_166414903.1|3050818_3051613_+|hypothetical-protein
MSTPVPPPPDAEPQREPTPLFAAPDGPPPASPDPWSLPVPAAAPPVVPESQRLVGYATEQHLGGAWDPRALSALAPAAPLAPRDGLAVPAFVLAWLVAPVGVVLGVVAAVRARRTGRRGVGLAAAAVVVGLAVSIVVPTLVAPSSEAWARAVGATGSLGEVRGATDAYARQLREGSCLADMPTGSTRRVTVVPCDSAHAARVVAVVPLRGDSWPGEAEVLRSVTDRCRVTAPAGADVVALTPSAAGWRAGDRNGLCLAGTTPGA
>NZ_CP049862.1|WP_166414904.1|3052015_3052852_+|C40-family-peptidase
MTPRTTDVVHGTAPSGGPSTSTPTRSRSARRTVATLVATLGIGLVPAVGTATAHAEPAAQSASADNSTRLSVTRSATTTYEGRKGSKLSIRLRNADEPVDGRVKVYDGKKLLRTLTASDRNDDGRLNLSYRLPKSLKVGKHTITLKFLPAASTDASSAKRTTKVRVRSEGELIVRTAKRYIGTPYRYGGTTPRGFDCSGFTSYVYKKAGVAKLPRSSSAQRGSGKVVARKNARPGDLIWTRGHVAIYVGNGKQIDAPRPGKSIKVRDIWQSNPTFLRV

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	2986774-2986798	3	0.88
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP029341	Streptomyces sp. SM17 plasmid pSM17C, complete sequence	18300-18324	4	0.84
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NC_020548	Azoarcus sp. KH32C plasmid pAZKH, complete sequence	287162-287186	4	0.84
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP009804	Streptomyces sp. FR-008 plasmid pSSFR2, complete sequence	3832-3856	4	0.84
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	LN997844	Streptomyces reticuli genome assembly TUE45, plasmid : III	69164-69188	4	0.84
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_AP014705	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence	482964-482988	5	0.8
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NC_020894	Streptomyces hygroscopicus subsp. jinggangensis TL01 plasmid pSHJGH1, complete sequence	78089-78113	5	0.8
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NC_017766	Streptomyces hygroscopicus subsp. jinggangensis 5008 plasmid pSHJG1, complete sequence	78090-78114	5	0.8
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	NZ_CP022366	Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence	625911-625941	5	0.839
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	NZ_CP007797	Azospirillum brasilense strain Az39 plasmid AbAZ39_p4, complete sequence	357926-357956	5	0.839
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	NZ_CP012917	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p3, complete sequence	540500-540530	5	0.839
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	NZ_CP032343	Azospirillum brasilense strain MTCC4038 plasmid p4, complete sequence	187701-187731	5	0.839
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	NZ_CP032348	Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence	384558-384588	5	0.839
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	CP023013	Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence	998539-998563	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP049794	Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence	1643932-1643956	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP049788	Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence	913715-913739	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP022766	Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence	1072780-1072804	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP021763	Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence	1090726-1090750	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP015116	Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence	1265932-1265956	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP049792	Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence	1419093-1419117	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052069	Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence	991730-991754	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP025986	Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence	1334885-1334909	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP022769	Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence	1080531-1080555	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP022773	Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence	795385-795409	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP022783	Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence	1004149-1004173	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP022791	Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence	906203-906227	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP022795	Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence	1000849-1000873	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP009763	Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence	999012-999036	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP022779	Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence	1080520-1080544	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052085	Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence	1086203-1086227	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052095	Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence	1113842-1113866	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052077	Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence	964280-964304	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052087	Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence	1086203-1086227	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052097	Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence	1113842-1113866	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052127	Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence	1086203-1086227	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052079	Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence	964303-964327	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052089	Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence	1086207-1086231	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052093	Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence	1113842-1113866	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052101	Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence	1113842-1113866	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052099	Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence	1113842-1113866	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052125	Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence	964303-964327	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP022793	Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence	1003322-1003346	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP022785	Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence	983997-984021	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP022787	Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence	1031943-1031967	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP022756	Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence	1078099-1078123	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052123	Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence	964303-964327	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052131	Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence	1086202-1086226	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052081	Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence	964303-964327	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052083	Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence	964303-964327	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052091	Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence	1113843-1113867	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP016613	Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence	1639190-1639214	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP021449	Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence	1422290-1422314	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP049790	Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence	1027922-1027946	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP016555	Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence	805147-805171	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP016915	Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence	1623409-1623433	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP016905	Ralstonia solanacearum strain KACC 10709 plasmid unnamed1	35566-35590	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052071	Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence	1168243-1168267	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP022482	Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence	86516-86540	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	CP023015	Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence	988523-988547	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052075	Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence	1168210-1168234	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052105	Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence	1167015-1167039	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052115	Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence	1167052-1167076	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052107	Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence	1167052-1167076	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP022781	Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence	963464-963488	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052117	Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence	1167041-1167065	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052129	Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence	1071325-1071349	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052121	Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence	1167041-1167065	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	CP011998	Ralstonia solanacearum strain YC45 plasmid, complete sequence	1095381-1095405	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052073	Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence	1168208-1168232	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052109	Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence	1167052-1167076	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052111	Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence	949670-949694	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052103	Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence	1167063-1167087	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052119	Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence	1167041-1167065	6	0.76
NZ_CP049862_2	2.1|61805|25|NZ_CP049862|CRISPRCasFinder	61805-61829	25	NZ_CP052113	Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence	949670-949694	6	0.76
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	NZ_CP026928	Agrobacterium tumefaciens strain 1D1609 plasmid pAt1D1609b, complete sequence	157981-158011	7	0.774
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	NZ_CP025013	Rhizobium leguminosarum strain Norway plasmid pRLN1, complete sequence	614985-615015	8	0.742
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	NZ_CP047181	Rathayibacter festucae strain VKM Ac-2802 plasmid unnamed1, complete sequence	1851-1881	8	0.742
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	NZ_CP053440	Rhizobium leguminosarum bv. trifolii strain CC275e plasmid pRltCC275eF, complete sequence	457844-457874	8	0.742
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	NZ_CP051295	Ralstonia solanacearum strain CIAT_078 plasmid megaplasmid, complete sequence	857131-857161	8	0.742
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	NZ_CP050100	Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b3, complete sequence	124977-125007	8	0.742
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	NZ_CP021083	Deinococcus ficus strain CC-FR2-10 plasmid pDFI2, complete sequence	95225-95255	8	0.742
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	NZ_CP047184	Rathayibacter sp. VKM Ac-2801 plasmid unnamed, complete sequence	13983-14013	8	0.742
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	MH807820	Dickeya phage Coodle, complete genome	144705-144735	10	0.677
NZ_CP049862_9	9.1|2325846|31|NZ_CP049862|CRISPRCasFinder	2325846-2325876	31	KY942057	Dickeya phage XF4, complete genome	143709-143739	10	0.677

1. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 3, identity: 0.88

gaggagggcgacggcgacgactcgt	CRISPR spacer
gaggagggcgtcgacgacgactcga	Protospacer
********** **.********** 

2. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP029341 (Streptomyces sp. SM17 plasmid pSM17C, complete sequence) position: , mismatch: 4, identity: 0.84

gaggagggcgacggcgacgactcgt	CRISPR spacer
gaggagggcgacggcgacggccccg	Protospacer
*******************.*.*  

3. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NC_020548 (Azoarcus sp. KH32C plasmid pAZKH, complete sequence) position: , mismatch: 4, identity: 0.84

gaggagggcgacggcgacgactcgt	CRISPR spacer
gaggagggcgacggcgacgctcggt	Protospacer
******************* .. **

4. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP009804 (Streptomyces sp. FR-008 plasmid pSSFR2, complete sequence) position: , mismatch: 4, identity: 0.84

gaggagggcgacggcgacgactcgt	CRISPR spacer
gaggagggcgacggcgacggccccg	Protospacer
*******************.*.*  

5. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to LN997844 (Streptomyces reticuli genome assembly TUE45, plasmid : III) position: , mismatch: 4, identity: 0.84

gaggagggcgacggcgacgactcgt-	CRISPR spacer
gaggagggcgacggcgacg-ttcacg	Protospacer
******************* .**.. 

6. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_AP014705 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence) position: , mismatch: 5, identity: 0.8

gaggagggcgacggcgacgactcgt	CRISPR spacer
gagaagggcgacggcgacgacggcg	Protospacer
***.*****************    

7. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NC_020894 (Streptomyces hygroscopicus subsp. jinggangensis TL01 plasmid pSHJGH1, complete sequence) position: , mismatch: 5, identity: 0.8

gaggagggcgacggcgacgactcgt	CRISPR spacer
gaggacggcgacggcgacgacgacg	Protospacer
***** ***************    

8. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NC_017766 (Streptomyces hygroscopicus subsp. jinggangensis 5008 plasmid pSHJG1, complete sequence) position: , mismatch: 5, identity: 0.8

gaggagggcgacggcgacgactcgt	CRISPR spacer
gaggacggcgacggcgacgacgacg	Protospacer
***** ***************    

9. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to NZ_CP022366 (Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence) position: , mismatch: 5, identity: 0.839

-acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
accgcgc-gcgcgccgcggcccgcatggacgt	Protospacer
  ***** **********.******.*****.

10. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to NZ_CP007797 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p4, complete sequence) position: , mismatch: 5, identity: 0.839

-acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
accgcgc-gcgcgccgcggcccgcatggacgt	Protospacer
  ***** **********.******.*****.

11. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to NZ_CP012917 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p3, complete sequence) position: , mismatch: 5, identity: 0.839

-acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
accgcgc-gcgcgccgcggcccgcatggacgt	Protospacer
  ***** **********.******.*****.

12. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to NZ_CP032343 (Azospirillum brasilense strain MTCC4038 plasmid p4, complete sequence) position: , mismatch: 5, identity: 0.839

-acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
accgcgc-gcgcgccgcggcccgcatggacgt	Protospacer
  ***** **********.******.*****.

13. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to NZ_CP032348 (Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence) position: , mismatch: 5, identity: 0.839

-acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
accgcgc-gcgcgccgcggcccgcatggacgt	Protospacer
  ***** **********.******.*****.

14. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to CP023013 (Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

15. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP049794 (Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

16. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP049788 (Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

17. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP022766 (Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

18. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP021763 (Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

19. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP015116 (Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

20. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP049792 (Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

21. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052069 (Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

22. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP025986 (Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

23. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP022769 (Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

24. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP022773 (Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

25. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP022783 (Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

26. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP022791 (Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

27. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP022795 (Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

28. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP009763 (Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

29. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP022779 (Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

30. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052085 (Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

31. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052095 (Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

32. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052077 (Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

33. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052087 (Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

34. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052097 (Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

35. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052127 (Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

36. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052079 (Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

37. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052089 (Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

38. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052093 (Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

39. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052101 (Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

40. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052099 (Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

41. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052125 (Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

42. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP022793 (Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

43. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP022785 (Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

44. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP022787 (Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

45. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP022756 (Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

46. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052123 (Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

47. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052131 (Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

48. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052081 (Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

49. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052083 (Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

50. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052091 (Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

51. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP016613 (Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

52. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP021449 (Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

53. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP049790 (Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

54. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP016555 (Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

55. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP016915 (Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

56. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP016905 (Ralstonia solanacearum strain KACC 10709 plasmid unnamed1) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

57. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052071 (Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

58. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP022482 (Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

59. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to CP023015 (Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

60. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052075 (Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

61. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052105 (Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

62. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052115 (Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

63. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052107 (Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

64. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP022781 (Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

65. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052117 (Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

66. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052129 (Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

67. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052121 (Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

68. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to CP011998 (Ralstonia solanacearum strain YC45 plasmid, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

69. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052073 (Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

70. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052109 (Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

71. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052111 (Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

72. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052103 (Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

73. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052119 (Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

74. spacer 2.1|61805|25|NZ_CP049862|CRISPRCasFinder matches to NZ_CP052113 (Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence) position: , mismatch: 6, identity: 0.76

gaggagggcgacggcgacgactcgt	CRISPR spacer
aaggagggcgacggcgacgaaggcg	Protospacer
.*******************     

75. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to NZ_CP026928 (Agrobacterium tumefaciens strain 1D1609 plasmid pAt1D1609b, complete sequence) position: , mismatch: 7, identity: 0.774

acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
gcgcggagcgcgccgcgatccgcaccgtgtc	Protospacer
.**** ************.****** *   *

76. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to NZ_CP025013 (Rhizobium leguminosarum strain Norway plasmid pRLN1, complete sequence) position: , mismatch: 8, identity: 0.742

acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
acttcgagcgcgacgcgacccgcaaggacat	Protospacer
** .  ****** *********** ****..

77. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to NZ_CP047181 (Rathayibacter festucae strain VKM Ac-2802 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.742

acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
acgcgcagcgcgccgcgcaccgcctccgagc	Protospacer
*****************  **** .  . **

78. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to NZ_CP053440 (Rhizobium leguminosarum bv. trifolii strain CC275e plasmid pRltCC275eF, complete sequence) position: , mismatch: 8, identity: 0.742

acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
aggagcagcgcgccgcgatccgcaaggcgat	Protospacer
* * **************.***** **  ..

79. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to NZ_CP051295 (Ralstonia solanacearum strain CIAT_078 plasmid megaplasmid, complete sequence) position: , mismatch: 8, identity: 0.742

acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
acgcgcagcgcgccgtgatccgcctgtcgga	Protospacer
***************.**.**** .*   * 

80. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to NZ_CP050100 (Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b3, complete sequence) position: , mismatch: 8, identity: 0.742

acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
aggagcagcgcgccgcgatccgcaaggcgat	Protospacer
* * **************.***** **  ..

81. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to NZ_CP021083 (Deinococcus ficus strain CC-FR2-10 plasmid pDFI2, complete sequence) position: , mismatch: 8, identity: 0.742

acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
cccaggtgcacgccgcggcccgcacggacgt	Protospacer
 *  *  **.*******.************.

82. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to NZ_CP047184 (Rathayibacter sp. VKM Ac-2801 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.742

acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
acgcgcagcgcgccgcgcaccgcctccgagc	Protospacer
*****************  **** .  . **

83. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to MH807820 (Dickeya phage Coodle, complete genome) position: , mismatch: 10, identity: 0.677

acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
ccgcgaagagcgccgcgacccgcaaacgttt	Protospacer
 **** ** *************** . .. .

84. spacer 9.1|2325846|31|NZ_CP049862|CRISPRCasFinder matches to KY942057 (Dickeya phage XF4, complete genome) position: , mismatch: 10, identity: 0.677

acgcgcagcgcgccgcgacccgcacggacgc	CRISPR spacer
ccgcgaagagcgccgcgacccgcaaacgttt	Protospacer
 **** ** *************** . .. .

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	305257 : 312107	7	Gordonia_phage(50.0%)	capsid,portal,terminase	NA
DBSCAN-SWA_2	1009662 : 1023981	15	Streptomyces_phage(66.67%)	tail,terminase,capsid	NA
DBSCAN-SWA_3	1084296 : 1102554	16	Aeromonas_phage(33.33%)	protease,tail,plate	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP049862|305257:312107|DBSCAN-SWA
GTCACGCGAGGACGGTCGCCTTGAAGGAGAGGTCGGCGTTCGCGAGGACCGGCATGCCGATCGCGTCGGACACGACCTCCGCGATCATCGGCGGCTTCTCGTTGCGGTACACGCCCGCGACGATGCCGGGCTGCTCCGACTCCTCGATGCCCCAGCCCGCCTCGGACGAGGACAGCGTCTGCCCCCAGAACGACGCACCGAGCTGCGTGTCCTCCCACGCGTCCGGCTCGACCGGAGCCGGGAGGAGGAGAACCTCCTTCTCGGGGAGGATGAGGCCCGACGCCGAGCGGCGCGTGTAGACCTCGACCGGGGGGAGACCGGCGCCCTCGATGATCGAGTTGACGTCCGCGACCGTGGCGGGACGCGAGCCGCCGCCGACGAGCGACGTCTTGAACTCGTCGCCCTGCGCGAGGACGCGGAGCGCCTTGCGCGACATGAGGATGGCACCCGGCGCGACGCCGTTCGTCGCCTCGTAGGCGTCCGACCACGTCTGCAGGTCCGCGAGACGCGAGACCGACGTCGCCGAGTCCCACAGCGCGGACGCCGTGACCGTGTGCGACGCCGACCGCCCGAAGGCGTCCGCCGCACCGATCTCGGGGATCGTCGCGACACCCGTCGACAGCACGACGCCACGGAGCCGCTCCATGCGGTCAGCGACCGCGAGAACGACCCGGCGCGCCGTCGAGAGGATCTGCTCGAGCAGGACGTCGTCCGACGCGTTGCGCGTGCGGAGCTGGTCGTACTCCGAGACCGGGATGTTCTGCCCGATCGCGGGGAGCTCGAGGACGGTGCGCTTACCCGAGGGGCGCTTGCCGACCGTCGGCTCGGCGTCGTAGGCGCGGAACTCAGCCTCGGGGACGAGCCCTGCCTGGCCAGCGATGAAGCGCACGACGATGTCGGGCACGACTCGGTTCGGGAGGAAGCGCGCGAGCGAACCGCGACGCTGCTCGACGGCCGAGAGGTCCTCGCGGATGTACCCGGTCAGCTCGGCCGGGGTGATGATGTCGGTCCAGAGAGCCATTGCTCCCCCTCTCAGACGTAGACGATCGTCGTGGCGGCGCGCTTCTCAGCGGCCACGGGAGCGACGAAGGAGTTGGGCACCTTGGACGCGCGGACGCGACCGTGGTCGAGCAGCGGGACCGCGAAGTCGGCGGTGCCGACGACGCGCTGGTCCGTGAGGATGAACCCGGCGAGAACGCCAGCGGCCGTCGTGGTGGCCTCGGTCTTGTCGTAGGGGACGAGAACGCCCCCGACCTTCGCGACCGGCGTACCGGACGGGATGTAGCCGTTGGGGTAGTGCGTTCCGGCGGTGAAGGCGGAGATGTCGAGGACCTCGGTGCGCGCGTTGGCGATGCCGTGCGTGGACCCGAGCCAGGACTGGTCGCCGCCGCCGAAGGTCTCAGTCGTGAGACGGGGCATGGTGGTTTCCTTCCGTGCGGATGGGGGTGTGGGTCAGGACTTCTTCGCGTGGCGACTGCTGTAGAGGTCGCGGCCGGCGGCCACGCTCTTCGAGTCGCCCTGCGAGCGTCGTCCCTGGCCCATGTCGGGCCACTTCTCGCTCTTCGCCGGCGCGATGCCGTCGACGAACGTCTGCACCTTGTCGGTGTCGACCTCACCGTCTGCGGTGAGGAACTTGGTGGGCTCGATGCCGTCGAGGACGGCGGTGAGCTTGTCGGCCGGGATGCGGCCGGAGTTGGCGGCGCGGAACTCGGCGGTGACGAGGCGTGCGGCGTACTCGCTGCGGACCTCGGCGCGGGCCTTCTCGGCGGCGCTGGTCGTCGCGGCGTCGAGCGCCTTCTCGTCGTCGGTGAGGTGCTTCGACTTGAGGGCGTCGCGCTCGGCCTTGAGCGTCTCGTAGTCGCTCATCGTCTTGACGCGGTCCTCGTGCTTGCGCGCCTTGTGGCGCCAGTACTCGCTCTTCTGCCCCTCGGTCATGTCCTTCACCGGCGTGTTCGGCGGGAACGCGTAGGTGTCGCCCGTGTCGGGGTCCTTGAACGAGGCAGCAGCCTCGCCCTCACCCTCGCCGCCGTCTCCCTCGGCTTCCATGCGGGCGTCACCGAACGTGAGGCGGTGGAACGCGAGCATCGCCTCGACGCCACCGGGCGCCGTGGGGTCGATCGAGTCGGTCGCGGGACGGTACAGGCTCTTGCTCATGCTGGTCTCCCTGTCGGAGGTCGGATGTGTCAGCAGCCCGTGACGGGCATGCCGTGGTCAGAGCGCGCGGAGCCGCGTGCCGAGCAGTGCGATGCGCTCACGCTGGTACGCGATCGCCTGGTCGAGTCCCGGCTCACCGGTTGCGGCGCGGGCCTCGAGCATCGGGAGCCGCGACTCGAGCGCGCGGATCTCAGCGGCGAGCATCCGGGCCGGGTCTACGGGCATCGACGGGCGCTGCGGGCCACGCGCACTCCGTGGCGCCGCACTGGGCCGCGTACCGGGGTGTGTCGAACGGTGCTTCGGGTCGACGAGCGTCGGCCCGAGCTCGGCGTGCTGCACGACGGTGAACCGCACCTGCTTGAGGTCGGCCGCGCCTGTCGACCCGGCCGCGTCGTAGATCTGCGCGAGCGTCTCGTCGTCGATCTCGCGACCGGGGTCGTTCTCGCCGAGGATCGGCATGGTCGTGCACTTGCACCGGTAGTGGATCGGCAGCAGCGTGTCGCGCGAATACACCCGCCCCGACGCCGCAGCGCACAGCCCGCACGTCCCCGTCGTCGACAGTTCAGGGCGGATGATGCGCCTGTACCCCGTGACACGCGGCGTCCCCGCGTACACGGCCCGCGACTGCCCTCGCCGTGCGAGCGCGAGGTCTGTGCGGACCATCGCGTCGACGCGGGTCTGCGCCCGTTCGACGGCCTCCCACCGGGACATCCCTGTGGACTCGAGGTAGCGCACGTGCTCGGCGACGCGCGCGTATACCTGCTCGTAGGACTCGACACCGGCGCGCAGCGGAGTCGACAGGTCGAGCACGCCGACGCTCTTCGCGGGCGCGTCGAGCATCATCGACAGCATGCGCGTCAGGTACGCATCCGTGGTCCCTGCCGCGGCGCGCGACGCTGACCGTGCGGTCGCGCCGATCTGCCGTGACAGCGCCTGCACGTCGGCAGGCATATACCAGGACTCGACGGCACCCACCGCGGCTACGGCGCGAGCGACCGCCTCGCGCTCGACCTTGGCCTGCGCGGCCGTCTCCATATCGACGAGCGACCGCGCACGCGCGACGCTCACGGCTGCACCGCGTCCCCAGCAGCATCGTCAGCAGGCAGTGCCGTGCTCGCCGCCGCACCGGTCAGGAAGAGATCGTCCACCCGCTCGGACTCCATGCGCGCGATCTGCTCGGGCGAGTACTGCCACACGTCACGCATGATCGTGTGCCACGGCACGTTGGAAGCCTTCGCCTTCACTGCCGCATCGGCCTTCTCCGCGAGCGAGTAGCGCTCCGCCGGCCGCCAGATGATGTCGAGATCCTCGAATCGCGACCGCTCCGTGTCGCCCGTCATGAGGAACAGCGCGGCGAGCGCACGAGCGTGCGTCTCCCCGAACCGGTCCTGCCGGTCCTCGATCTTGAACGTCCGACCCTCACGAGCGAACGCCGAGCCAGCAGCCGACTGGTTCTGCCCCTCAGGCGAGAACATCGCCAGCGGCGTGAACGTCACCGCCGACAGCTGCTGGGTGAACTTCTCCATGCCGGTCCATACGGGCGTCAGATCGACGTTCCCCGACTCCCAGAGGTCAGCCGTCGGGGGCAGGGTCCACAGCGACCCTGGGTCGGCGGAGAACACGTCGTTGTAGTCGATCTCAGCGCCGGTCTCAGGGTCCTCGGCGGGCATATCCTTCGGGTCGATCTTGAGCGCGCGCTGACGGAACGCCTGGTAGGTCGCGATCGACATACCCTGCAGCACCATGTGATCCAGGCGGTCAAGCAGGTCCCGGTGGCGCTGAAACTCGCCCACGCCCTCCTCGTTCCGGTACCGGAACACAGGCACGAGCTTCTCGCAGCCCTCGGGGAGCGCCTGCCCCTCTTCGCCGCCGAACTCGGGGTCCCATTTCCACGACGACGCGAACCGTGCGCCGTTCGGTCGCTTGCGGTCCGTGAATGCGCGCCACACCCGGCCGGGCCGGTAGAGGTACGCGTAGGCGCGTTCGTCGACGTCGTGGTGGAAGAACTTTGCGGCGGCGAGCACCTCGGACTGCACCACGGGGTCGTGGATCGTCACGACCTGCCGCGGGTCCTCCGACGTGTACCGAGGCTCATCGCCGTGCATGCCGACGATCGCGTAGCCGTTGCCCGCCGTGAGCGCGAGACGGATCGCGTCGTCGCCCTCCGTGCGCATGCCCGAGCGGACGACCATCCGCCACGCCGCCGGGTCGCCGCCCTCGCCCGTGTCGACCCCGGTCGCAACACCCTGCAGCCGCAGGGGGTACTTCACCGACTTCACGATCATCTCAGCGAACGCGGTACGCGCCGCCTTGAAGAATCGCTTCGCCGACTCCGGAGCGTCACGCAGCGACGACGGCACCGGGGCGTCGCCCTCGTAGCGAGCGAACAGGTCGCTGACCATCTTCTGACGGTCGTCCATCTTCCGCGACAGTCGCTGCAGCCACCAACCGGGGCTCTGCACAGTCTTGACGTCGATGCTCACGCGTCGCCTCCTGTCACCTGATGCGTCGTGGGCGAGCGGGAACGTGCGGCTTAGCCTGGCCGGCCTTCACGCCGTCGAGGTACGCCTGCCACGAGAGCATGGCCGCCATCGCGGCATCGAACTTCCGGTCGGGGTGGATCTTCCCGAGGATGTACAGCGGCTTACCCTCGTCGTCGACGATGTTCTTGAGCTTGACCTGCCCCGCCGCCGCGATGTGCCGCGCGAGCTCGGGAGCGTGCGGGTCCGACGCAGTCCAGCCGACCGCGCCGGACGCGATCGCCTCCTGGTACGCGCGTATCGCGTAGGCCGCCTTCTTGTAGTGGTTCGTCCACCACTCCTCGACGAGCCCCTTGTGCCTCCCGGCCCACACGCCCATCTCGGTCACCCAGTACGGCGGGTCGCCGTACAGGCGCCACACGTTGTAGCGAGAGAAGATGTGCTCGACCGTCTGATCGACCTCAGCCTCGGGGACTTCCCACTCGTCGTCGTCGAGGTCCTTCTCCCACAGGCCAGCGATCTCCTGCGTGCCCGTGAGCAGGTCCGTGATGACGAACGCCGTCGAGTCACGACGGCGCGCACCGTCGAACCCCACCGCGACCGGCGCCCCCGCAGGGATACGACCACGCAGCGGCTTGTCGACGTCACCGCCCTCGTGCTTGAGATCCGACCAGCGCTTCACATCGAACGCCTGCTGCCCCGACTTCACCCAGCGGTTCAGCCACACCCGCTCGAGGTACGCCTTGTCCACGCCAGGCCGGTCCCACTGCGACGCGATGTCGTCGAACTGACCCGGACCCCACTCGCCGGCGGGACCGGTCGCCTCAGCAACCGCCTTGGTCCTCTCGGCCTTCACCTCGAGGTCGTGCCCGCCGTCGTCCGTGCGGTACAGGTAGAACAAGTCAGGGCGCTCGATCTTGCCGTCCCGGATCGCCTCAGCCTCAGCGTGCAGGTTCTCCGCGACCGACCCCTGCCCGAGCTCGCCCGCCGTCCCCACGTACAGCGACCACGGGTCCTCGAGCGGGCGCTTCGCAAGGTTCGCAGCCATCGTTTCGTGCGCCTTGATGTGCCGAGGCAGATGCAGACGGTGCGGCTCGTCGAACGCGTTCAGCGTCGTGCGGCCACCGTCACGCGAGTCCGGCGCGTTCGCCAGCGGCCATGCGCCACCGTCCGAACGCCCCCAGTCGTCGAGCCGCAGCGCACGCTCGAGCGACACGTCGAACAGATCCGAGTCCGGGCCGTTCTCGATGACGTACTTGAGCGCCCCATAGGCGAGCTCTTCGACCTGGTCGAGCGAGAACGCGAGCATCGGCACGTAGGGCGACATGACCGGCGCAGCCACAGGGTGCCCGTCGGCGTCGAACCCGTCGCACTTCCCAGGCCCCTCAGGGTGGATGTGCGCGTAGACGAGCAGCGCTTCCTTCTCCGTCTTGGCCAGGCCCTTGCGGACCGACAGCCCGCCACGCTTGAACCGACGACGGCCAGCCCACGGATGGCCCTGCGGGTACACCTCGAACAGCCTGTAGATGAACGCCCGGAACTCCGGGTCGATCACATACGGCTGCCCCTGCAGCGACCCCGGACCGTAGACCGCACGCTCCTCGATGAAGTCGCAGACCTCACCGCCGATCGTCGGCCACGGCTCAGCGTCCGCACCCGGAACGACGAGGAGACCCATCAGCCCACCGCGTACAGGCCGCCGCGCGGGTCCTCACCCGACTTCGGCTTCGGCTTGCGCGTCTCACGACGACGCTCCCCGCGGTCCTCCGCCTCCTCCGCGCGCTCGATCTCCGCACGCAGCGACATCAGCGCCTTCGGGTTCAGGCCCAGCCGGTCAGACAGCATCCGCGCCTCAGTGGCAGCCTTGAGGTCGCCCTGCTCGGCGCGGATCTTCCAGCGCACGTACTGAGCAACCTCACGGCCCGAGTGGGACTCCTCCCAGATCGCAGCCTGCGGCATCGCCCACAGATCAGCCCACAGCGCGACCTCAGCGTCACGCGCCTGCTCGATCTGCAGACCCAGCGTCGCCACAAGCATCTCGTTCTTGTTCAGATCCCGACGCAGACGGCCCTTCGTCCGACCGTCCTCCGCCTCCTCGACCTCGACCTGCAGAGCAGCCACACGGTCACGAGCGAGCTCGAACGCCGCCTGCTTCTCGACGTCAGGCTGCAGCGGCCACGGAGGGACCGCCGCACCCTCACGGCCATCAGCCGGCAA

Protein sequences of DBSCAN-SWA_1

>NZ_CP049862|305257:312107|309906_311568_-|WP_166412738.1|terminase|DBSCAN-SWA
MGLLVVPGADAEPWPTIGGEVCDFIEERAVYGPGSLQGQPYVIDPEFRAFIYRLFEVYPQGHPWAGRRRFKRGGLSVRKGLAKTEKEALLVYAHIHPEGPGKCDGFDADGHPVAAPVMSPYVPMLAFSLDQVEELAYGALKYVIENGPDSDLFDVSLERALRLDDWGRSDGGAWPLANAPDSRDGGRTTLNAFDEPHRLHLPRHIKAHETMAANLAKRPLEDPWSLYVGTAGELGQGSVAENLHAEAEAIRDGKIERPDLFYLYRTDDGGHDLEVKAERTKAVAEATGPAGEWGPGQFDDIASQWDRPGVDKAYLERVWLNRWVKSGQQAFDVKRWSDLKHEGGDVDKPLRGRIPAGAPVAVGFDGARRRDSTAFVITDLLTGTQEIAGLWEKDLDDDEWEVPEAEVDQTVEHIFSRYNVWRLYGDPPYWVTEMGVWAGRHKGLVEEWWTNHYKKAAYAIRAYQEAIASGAVGWTASDPHAPELARHIAAAGQVKLKNIVDDEGKPLYILGKIHPDRKFDAAMAAMLSWQAYLDGVKAGQAKPHVPARPRRIR
>NZ_CP049862|305257:312107|308474_309893_-|WP_166412737.1|portal|DBSCAN-SWA
MSIDVKTVQSPGWWLQRLSRKMDDRQKMVSDLFARYEGDAPVPSSLRDAPESAKRFFKAARTAFAEMIVKSVKYPLRLQGVATGVDTGEGGDPAAWRMVVRSGMRTEGDDAIRLALTAGNGYAIVGMHGDEPRYTSEDPRQVVTIHDPVVQSEVLAAAKFFHHDVDERAYAYLYRPGRVWRAFTDRKRPNGARFASSWKWDPEFGGEEGQALPEGCEKLVPVFRYRNEEGVGEFQRHRDLLDRLDHMVLQGMSIATYQAFRQRALKIDPKDMPAEDPETGAEIDYNDVFSADPGSLWTLPPTADLWESGNVDLTPVWTGMEKFTQQLSAVTFTPLAMFSPEGQNQSAAGSAFAREGRTFKIEDRQDRFGETHARALAALFLMTGDTERSRFEDLDIIWRPAERYSLAEKADAAVKAKASNVPWHTIMRDVWQYSPEQIARMESERVDDLFLTGAAASTALPADDAAGDAVQP
>NZ_CP049862|305257:312107|306708_307410_-|WP_166412735.1|DBSCAN-SWA
MSKSLYRPATDSIDPTAPGGVEAMLAFHRLTFGDARMEAEGDGGEGEGEAAASFKDPDTGDTYAFPPNTPVKDMTEGQKSEYWRHKARKHEDRVKTMSDYETLKAERDALKSKHLTDDEKALDAATTSAAEKARAEVRSEYAARLVTAEFRAANSGRIPADKLTAVLDGIEPTKFLTADGEVDTDKVQTFVDGIAPAKSEKWPDMGQGRRSQGDSKSVAAGRDLYSSRHAKKS
>NZ_CP049862|305257:312107|305257_306277_-|WP_166412733.1|capsid|DBSCAN-SWA
MALWTDIITPAELTGYIREDLSAVEQRRGSLARFLPNRVVPDIVVRFIAGQAGLVPEAEFRAYDAEPTVGKRPSGKRTVLELPAIGQNIPVSEYDQLRTRNASDDVLLEQILSTARRVVLAVADRMERLRGVVLSTGVATIPEIGAADAFGRSASHTVTASALWDSATSVSRLADLQTWSDAYEATNGVAPGAILMSRKALRVLAQGDEFKTSLVGGGSRPATVADVNSIIEGAGLPPVEVYTRRSASGLILPEKEVLLLPAPVEPDAWEDTQLGASFWGQTLSSSEAGWGIEESEQPGIVAGVYRNEKPPMIAEVVSDAIGMPVLANADLSFKATVLA
>NZ_CP049862|305257:312107|307467_308478_-|WP_166412736.1|DBSCAN-SWA
MSVARARSLVDMETAAQAKVEREAVARAVAAVGAVESWYMPADVQALSRQIGATARSASRAAAGTTDAYLTRMLSMMLDAPAKSVGVLDLSTPLRAGVESYEQVYARVAEHVRYLESTGMSRWEAVERAQTRVDAMVRTDLALARRGQSRAVYAGTPRVTGYRRIIRPELSTTGTCGLCAAASGRVYSRDTLLPIHYRCKCTTMPILGENDPGREIDDETLAQIYDAAGSTGAADLKQVRFTVVQHAELGPTLVDPKHRSTHPGTRPSAAPRSARGPQRPSMPVDPARMLAAEIRALESRLPMLEARAATGEPGLDQAIAYQRERIALLGTRLRAL
>NZ_CP049862|305257:312107|306288_306675_-|WP_166412734.1|DBSCAN-SWA
MPRLTTETFGGGDQSWLGSTHGIANARTEVLDISAFTAGTHYPNGYIPSGTPVAKVGGVLVPYDKTEATTTAAGVLAGFILTDQRVVGTADFAVPLLDHGRVRASKVPNSFVAPVAAEKRAATTIVYV
>NZ_CP049862|305257:312107|311567_312107_-|WP_166412739.1|DBSCAN-SWA
MPADGREGAAVPPWPLQPDVEKQAAFELARDRVAALQVEVEEAEDGRTKGRLRRDLNKNEMLVATLGLQIEQARDAEVALWADLWAMPQAAIWEESHSGREVAQYVRWKIRAEQGDLKAATEARMLSDRLGLNPKALMSLRAEIERAEEAEDRGERRRETRKPKPKSGEDPRGGLYAVG

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_166412733.1|305257_306277_-|capsid	major capsid protein E	A0A166XYQ6	Gordonia_phage	5.0e-74	45.8
WP_166412734.1|306288_306675_-	potassium transporter	Q6VY52	Streptomyces_phage	1.7e-14	39.5
WP_166412735.1|306708_307410_-	hypothetical protein	NA	NA	NA	NA
WP_166412736.1|307467_308478_-	hypothetical protein	A0A1B3AY77	Gordonia_phage	2.0e-30	44.9
WP_166412737.1|308474_309893_-|portal	phage portal protein	A0A1C9EI50	Rhodococcus_phage	2.5e-55	33.3
WP_166412738.1|309906_311568_-|terminase	large terminase	A0A159B6A7	Gordonia_phage	3.0e-161	53.4
WP_166412739.1|311567_312107_-	hypothetical protein	A0A162E1R7	Tsukamurella_phage	3.4e-05	32.7

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP049862|1009662:1023981|DBSCAN-SWA
CCTAGTTCTCTCCGACGCGGCGGAGCTCGTTCTGCCCCAGGCGCGTCACGGCCATTGCCGTGGTCGGTGTCCTCATCTCCGCGCGGACCACCTGGCGCGTCAGGACCTTGACGTCCTCGCCCGTGATCGGATTGCGCACGTAGATGTCGGGGATCGTCACGTAGACGGGAGCGGGCGTCGGGGCGTTGATTGGGGCCGCGACGGGCATGTTCGCGGCCACGGGACCGCCGTTTCGGAGGCCGGGCAGGTTGCCGTTGAGCGCAGTCCGCCGAAGGCCTCCAGCGCGGCCATCCCCACCCCGCGCGGCGACATCTTGAGCTGTGACGGCACGGGGTGCACGGATGTCGCCGCTCGCACCCGGATCGGGGCCGACCGCGACGGTACGGGGTGCACGGATGTCGCCGCTCGCGCCCGGATCGGGGCCGACGGCGATGGGCGAGCTGTTGGCGGACGCCTTGACGATGTTGCCCTTGGAGTCCCGCTTGAGTCCGAGCGACGCCAGCAGTGCGTTCTCCATCGTCACGCCCCACGCCTCGATGGACGCAGTGACCGAGCCGAGCTGATCCTCGAGGCCGTCGACGATGGCTTCTGCGGCCTCCACGCCGCCCCTATAGAAACGGCCGTCGATGGTCGTGTTCTTCGTCGCGGACGCCCCAGCGGCCTGCGAGTAGCGGTCGATGTCCGCGTACGCGCCGTTGAGCGCCTTGATCGTGGACGGGTCCGCCAAGAGCGCGTCCGCGAGCGCGGTGCCCCCCTCGAGGCCCTCGTGTGCGATCTCCTGGAGGATCACACCCGCGACGCCGGCCGCAGCGAGCTTGTCGAGCTTGCCGCCGAACGTCTTGAGGTCGCCGGCCTTCTTCTGCGCAGACGCGAGAAGGCCCTTGGCTGTGACGGGCTGGTCGTACCCGTAAGCGTCCTTCTTGCCGAGGGAGTCCGACAGCTTGAACTCGCCGGCGAGGACACCGGCGACGGACGCCTTGATCGAGGCGAGCTGCTGCGTGTGATCGCGGGCGGTGTCGAGCTTCTTCTCGATGCCCTCGGCCTGTGCGTACAGCTTGCGTAGCGCGACCTCGGCCTCGCGTGCGGTCTTGGCGAGATTCGCCCGCTGCGCCTTGGACAGGTCGGAGTTCTTCGACTGGTCGCGCAGCGTGTCGACGACGGAATACGCACCCGACAGACCCGAGGACACCTGGTCGGTGATGTTGCCCCGACGGGCATCGACGGCGAGGTCGGCGCGCGCGTCGGACAGCCGGGACTGCTTTTCGCGCTCCTCAGCGCGCTCCTTGCGCGCGTCGTCGAGCGCCTTCTCCGCGTTCTTGAGCGCGGCCTTGGCGGCCTTGAGGTCCTTGCGCTCGTCGTCGAGCTGCCGCTGGGCGGTGCGCTTGCGGTCGCGGTTCTTCTTGTCGCCTGGGATGTCGCGCCAGCGGTTGAGCGCGGACTCGACCTGCCGCTCCTCGCGCTTCACGGCGGACCGCGCACGCTTGACCGCTGCCGTCGCGTCCACGACAGGATCGTTGGCGCCGACTCGGCCACCGGCAGCGAAGGCCGGCAGCGCGCGTCCAGCGAGAGCGGCCGCGCGCCACTTCGTGACCTGTGCGTGCCCGCCCATCGCGGCAACCTCGCGGGCCGTGATGACGTGCTCGCCGTTGGACAGGCGCGCGAGGATGTCGTCGCTCGTGCCCGTGCCCGGACCGACGACGGCGCCGCCCGTGGCCTTGGCCTGGACGTGAGTCTTGCCCCCACCACCAGAGTTGGTGACGACGTTGATCGCGATCTGCCTCTTCATCTGCTCGCGGATGAAGCGCGTGACCTCCGCCGAGGCCTTCGAGGTGTCGACGTCGACCTCGGTCTTGATGTTCGACGGGATGAGCCCGAGCTCGTCTGCCAGCTTCTTCGCGGCCTTCTCCGAGAGGCCCATCTGCTTGGCCGCGTCGACGAACTCGCGGCGCGTGCGGCCCATCTTCTTCTGGAGCTGCTCGTCCGTGGCGCCCTGGGCGCGCATCTGGTCGATCCACTTCCAGCCTGCGTCGGCGATGCCGTCGAGGACAGCCTGGTTCGCGCGCCCCTTCTCCGTACCGACGTCGAGCGTCTGGCCGTTCTTCTTGAGCGACTCGTTGACGGCGTCGAGCGCAGCCTCGTAGCCACGCTCCGCGTCACGCATGCCGAGCACGCCGTCGGCGAGACCCTTGATGGCCTTCCAGGCGGCGTCAGCGGCCTTCGCCTGGTCCTCGAGGTTCGTCGCGAAGAGCTCGACGGACTTCGCGGCGCGGTCGGTCTCCTCGGACGTCGCGCCCGTGGCCTCCGCCATGAGCTCGTGCTTCTTCTTCGCGGCGTCGAGGTCCTTCGACTGGCCCTGGAGGCCGCGGCGCAGCGCACCGACCGCATCGTTGTAGTCGCCGATGGAGAGGCCGTTCTTCTCGGCCTCCTCGCGGATGTTGCCGTACGCGACCTCCTGGGGACCGTAGTAGCGCTCGAGCGCCGCCATCGCGTCCTTCTGCCCAAGGATCGCGTTCGTGACGGTCTCGACGCTGATCCCGAGCGCCTCTGCGCCCTCCGCAGCCGAGCCGGAGAAGTCGAACGTCCACCAGTCAGGGGTCTTGACGAGCTCGGCAGCGATGACCTGCCGCGTGGACTCGGTGACAGCACCCGTCACGCCGTCGAGGGACTCGCGCAGGGAGTCGATGCGCTGCTTGGACTCGGCCTGGGCGTTGGCCCACGCCATGACGCCGATGGTCGCGACACCGATCGCGGCGGACACCGCGCCGACGGCGACGCTCGCGCCCTTCGCGGACAGCTTGAGGCCCTCCGCGGCGTTCTTCGCGTTCTTGAGACCGCCGACGAGCTTCGTCAGGCCGGCGACGCCGAGCGCGGTCATGCCGCCCGCGCCGGTGAGGACGGTCAGCACCTCGAGCACGGGCCCGGGGACCTCGCCGATCGCGTCGACGAGCGCGCCGGCACCTTGGGCCATCTCGCGCAGGACGTCGTTGGCGCCGCCGCCCGCCTGGATGAAGACGGTCTCGATGGAGCCGGACAGGGTCTCGAGGTCGCCCTTGAGGTTGTCCATGCGGATCGCGGCGACCTCGGACGCGTAGCCCTGGTCGTTGACCGCGGCCGTCCACTCGCGGACGCCGTCCGCGCCGTTCTCGTAGAGGGCGTTTGCGGCGCGCACCGCGTCCGCACCGAACATGGTCGCCATGGCGGCGTTGCGCTGCGCGGGCGTCATGTCGCCGAGCGCGTTCGTCAGCTGGCCTGCGAGCTGCTCGAGGCCGACCCACTGCCCGGACACGTCGTACGCCGAGATGCCGAGGGAGTCCATGAGCTGCTTGGCGTCGCCCATCGGCGCGGACAGGCGCTGGAGCATGGTCTTGAGGGACGTGCCCGCGTCAGACCCGAGGAGGCCTCCCGCAGCGAACGCCGCCAGGGCTGCGGTCGTCTCCTCGATGGACAGGCCGGTCGCGGATGCAACCAGACCGCCCTGCTTGAGGGCCTGCCCGAGGTCGCTGACCTCACCCATCGCCTTGCCGGCGCCCGCCGCGAGGAGGTCGGCGACGTGCCCGACGTCGCTGCCCTTCAGCTTGAACTGCGTCATCGCGATGGCCGCGTACTCGGCGGCCTCGGCGACGCCGAGGTTTCCGGCCGCAGCGAGGTCGAGCGAGCCCTTGAGGCCGCCCGCCAGGACGTCCTTCGCGGTCACGCCCGACTTCGCGAGCTCTTCGATGCCGCCTGCGGCCTCGGTCGCGGAGTACTTCGTGTCCGCGCCCGCCTGGATCGCCGACGCGCGCAGGCCGTCGATGTTCTGGCGGGCGTCGTCGCCGGTCGCGGCGACACCGGACATGCCCTCGTCGAAGTCCGCGAAGAACTTCACGGCGATGCCCGCGGCGGCGGTCAGTGCGCCGCCGACGAGCGCGGTGCGGTTCGCGAGGTCCTGCGCCGCCTCGGACTGCAGGCGCGACGCGATGGTCGCCTTCTTCGACGCCTCCGCGCTCGCCTCCGTCGCCGCGGCGCTCGCCTCCGTCGCGCTGCGCACGTTGCGCTCGGCGCGCTCGAGCTTCGACGCCGAGACCGCCTGACGCTCGCGCGCCTGCTGGAGGCTCTTCTCGGCGGCAGCGACCTTCTCCTGGTCACCGCTCTTGCGCGCGTCCGCGAGAGCCTTCTCCGCCTTCGCGACCGCGTCCGCCGACCGGGCGACGGCGTGCTGCGCCGCGACGAGCGACTCCCCAGCGCGCGCGGCCTTGTCCGCGGCGGCCTGGACCTTGCCCATGCCCTGCGCGACGCCGTCGAGCTTGCGTGCGGAGTCCTGGTCGTCGACCTTGATGTAGGCGACGAGCTCGCCGACGGTGAGCGACATTGCACCTCCCGAGGGCGTGGTTCTGGTGGGGTCAGGGGTGCAGGTCGCGTGCGAGGCGCGAGGTCGGCTCCGTCAGGAGCGCGAGGATCAGCCCGCGCAGCCACGGCCACGGGCGCGCGTCGAGCGCGGGGTCGTACAGGTCGACGCCGTAGAGGGCGAGCAGGTCGACGGTGATGAGGTCCCAGCGGTCGAGCAGGTCACGCCACGTCGGGCCCGTGGTGGGCGCGGTGGGTAGCTGCTCGCGGGGTGGGCGGCGGTAGCGCGGGTAGATGCCGTGCTCGTCGGGTTCGCCGATGCCGTACGGTGCCCAGTCCGCGGGGCCGCTCAGGCTTTTGGGGCCGCGCCCTCGTCGTCGGCGGGGCCGTAGGTGAACTCCATGACCTGGTCGGCGGCGTCCTCGCCGAGCGTCCAGTAGTACTGCGCGTACAGCGCGTACCGGTCGACGTCGATCTCCGGCTGCCCGTCAGCGAGCATCTGGTCGTACACGGCCTGTGTGAGCGCGAGGTGCCCCACGGGGGTGTCGCCGGGGATGGACTCCCACAGCGCCATCGTCTCGTCGTCGGTCTCGCGGCCCGTGGCCTTGTTCATGCCGTAGGCGACGATCGCGGCCAGGACGAGCCCGTTGTGCTTCGTGGGCGGCGGGACGTGGTAGATCTTGCCGTCGCGCGCCTCGAGGTCGAGGTTCGGGCGGAGGTAGCGGGTGAAGGACTTGGCCACGGCGGTGCTCCTTGCTCTGGGTTGTGGGTGCGGGCGAGCCCGCCCGCCCACAGCGGGGCGGGCGGGCTCGAGTGCGGTCAGGCGCCGCGGGTGTACGGCAGCGCGTTCGACGCGCCGTTCGTGGGGTGCGTGACCGTGATCGGCGCGGACCCGGCCGACCCGGCGGGCACGACCGCGACGATGGTCGAGTCGCCGACCACCGAGATCGACGTCGCCGACGTCGCGCCGACCTTCACCGCGGTGGCGAGCAGGACGCCGGCGAAGCCGGAGCCCTTGATCGTGACGATGTCGCCCGCGGCCGCGGCCGACGGCGCTGCCGAGCCGAGCACCGGGGGCGCGCTCGGCGAGCCACCGGCCGGGGCCGGGTTGGCGATCGGCTTGATCTTGCCCTTGCCGGTGAGCGTCGCCGACCAGCCGCCGAGGTCGGCGTTGCCGGTGTTGCCGCGGTCCATCTGAACCGAGTAGATGCCCTGGAACGCGTAGTCCGCGCCGAGGCTGTCGTAGACACGGACCTCGGCGAGGGCGGCGTTGCCGCGCGTGCCGGGCTTCGCGGCGTTGAGCAGCGCCTGGACCTCCGGCAGGAACGACCCGTCGGGGTTGCGCTGCGACTGGATCGTGAATGCGAGGTTCGCCGACTCGCCAAGCTTGGCCTGGTTCTGGGCGCCCTCGTCGTCGTACGTCGCGGCGTCGACGAGCGTCGGGGCGTGCTGGGGGTTGATCGCGCTCGTGAAGCGGATCTGCTGCCAGATGGCGGGCGTGACGCCCGGTCCGGCGAGGTTGATGTCGAGGTCGAGCTCGTAGGAGAGCCCGAGGTCGGTGGGGACAGACATGAGGATGCCTCCGGGGTGTGGGATGGATGCCGACCCTCGGGCGGGCAGGCAGTGGACCGGGCCGCGCCCGCCAGGGACGCGCGCTCGGGGATCAGGGCAGGAGGACCTCGTAGTTCATCGAGACCTCCGGACGACCGTTCGAGTCCAGCCCGAGCGGCAGGTACGAGCGACGGTGCACCCGCGTGATCGCCACGCCCGACCACGTCACGTGGTGCGCACGCAGCACGGCGTGCACGGCCTCGGCGAGCGCGTCCGCGCTGTCCGGGCGGCCCTTCGCCGCGCGGACGCGCACCTGCACGCGCACGCGCTCGTCCGTCAGCCGCGGGTCGGCGTGCTCGTCGCGGTCGTACACCGTCAGCACGACCGCGCGGTCCGGGGCGGCGGGCATGACCGTGAGGGTGATGCCGGTCTGACCGGGCGTGTAGATGCCGGCGGGGTTCCAGGTGGCGACGCCTGCGGCGTGCAGGCGCTCGGCGAGCGCCGTGTAGAGGCTGGTGGCGGGGACGGTCATGCGAGCCTCCCGCGGATGGTCTGCGCGATCGCGGCGAGCGCCTGGTCACGGTGCTCGAGCAGCGGGCCCTCGAGGTACTTGGCCTGTCGGCCCTCGTCGTGCCGGTAGTCGAGCTCTTCGTGCTGGCGGACGGCGTACGGGGTGTCGTAGGAGACCGACGCGGTGAGCGTCGCCTCGTCGACGTCCGTCGCGCCCGAGCGGGAGAGGGTCGCTTCCTCGATGGGGACGACCTTGCGGGACTCGGCGAGGACGACCTCCGCGCCGACCTTGAGGCCCGCCGCCGCCGCGGTGCGGAGCGCGGCCTTCGTGGCGCCGAGGTTGAGGGTGAGGGTGGAGCGCATGGCCATGCCGGGTCACCTCACGTCAGGGAGAGCTCGTTGTGCTCGGGTGCGGGCGGCGTGTGGTGGTGCGCGACGGCGAGGACGACGGCGGTGCGTCCGGACGGAAGGTCCACCTCGGAGTCGAGCGGCACGGGGCCGTGCTCGGGCCGCAGGAACACGCGCGCCGAGGAGACGACCTCCTGGCCGTTGCGGTCGCGCACGAGGCGCGTGGTCTCCTCGACGCGAACGTGCTCGAGCGTGCGGTCGGGGCCGAGGACGGTGCCGTACGCGCCGGTGCCCTCGGCGTTGCGGACGGTGACGGTGTGCGGGGTGAGGATGCGCGGCAGCTTCATGGTGTCCTCGGTGCGCGGCCGATGAGGCCGGCGTTCTGGAGGATCGTGATGGCGCGCGGTGCGACGAGGGATGCGGCGGCGTCGGTGTTCGTGCCGGAGCCGACACCGCCACCGGAGACGGAGAACGACCCGAGGGAGAGGCTGTTGTAGCGGGCGGCGGCGCCCGAGGTGTCGCCGGTCTCGTCGAGCCACGCCACGGTCGCGCACGTCGCGTCCCGCAGCGCGGCGCGCACTACCGGGTCGGTGGGGAGTCCGTCGGTGTCGACTTCGTAGACGGCGGTCATCGTGAGGCGTTCGACGTCGGCGGACGCGAGCGCGATCAGGTCCTCTGCGGCCTCGGCGGACAGGCCGAGTCGCCACGGGGACCCGTTGACGTCGGCGAGGGTGGCGTACGTGCGCACGATGAGCCTCCAGGAGGGGTGTCGGGGTGGGACGCAGGTCGCGGCGCTACAGCCAGGAAGGAGACCGCCATCGGTGTCCCGGCCAGCCGGCCTTCCGCCCTGTACTCGTGTGTGGCGGGGGCGGTTGACGCCCCACCCCGAAGTTCGTGTAGTGCTGTCCCCGCCCCCGGTCAGGGGCACGAGGGCGGGGACAGTCCAGGGGTGGAGGTCAGGCCTCCGGGGCGACCGTGTAGCCGCGGCGCGTGAAGTACGCCAGGGCGACGGGGTCGCTGGTGTGGGCGGTGCCCTTGGTGAAGGTGACGCCGAGGACGTCGCCGGTGAAGTCGGTCGCGGGCGAGTGGACCTCGACCTCGACGGGCTCGGCGTCGGCGGGCTCGGTGGTCGGGACCTCCGGGTCCGTGACCTCGGGCGTGACGACCTCGGCCTCGGGCGTGACGACCTCCGGGGCCTCCGGTGCGGGCGCGTCCTGCGCCTTGCGCGCGGCCACGGTCAGGCGACCTTGATGTTGCGGAAGACCGCCGCGGCCTTCGTGGCCTTGAGCGCGACGGCGACCGGACCCATCTCGACCTCACCCTTCTTGACCGCACCCGCGGTCGAGAAGTCGGGCATCCACGTCTCGACGAGCTGGCCGCCGACCGTCGCCACCGCGTGGAAGCCGTCGAGGCCCACACGGATCGCGTACAGGTCCGTGAGGCCCGTCTGCGCCGTGCCGACCGTGCGGTTCTCGATCGGGATGATCGGGTTGTTCGACCCCGCCTTCGCGCCCGGGTCGGCGAAGATCACGTCGCCGTACGCCTCCCGCGTGATCGGACGCCCGTTCGGGCCGAGGAGACCCTCGACCGGGTTCTTCGTGTACATGCCCGCACGACGAGCCGCGGCCCGGACCCGGGCGAGCGCCTTGGCGTTTCCGAGGAGGACCGTCGGCGAGCCGTCGAGCAGCGCGAGGAACTCGTCGATCGCGTCGAGCGCCTTGTGCTCCGCACGCGAGTCCGTGTCGAAGTCGGTCCAGTCGGTGACCGACGTGGCGCGGAACTCCGTGGCGGAGCCGGTGAGCGCCTTGTCGAGGCCGTCGAAGCCCTTGGCGTCGACGGCGACGTCACCGTTGATGACCTCGTCCTGGAACCGGGTCGTCGTGGCGGTGATCGTGTTCTTGAGGTTGAGCGCGACGGACCCGGACGCGGCCGGGCCGATCTTCGCGATCACGCGGTCGACCTCGAACGCGCCACCGAGCGGGACCAGGCTGACGGTCTTGTGCTCGGTGGTGACCTCGGCGGTCGTGTACTCGCTGTTGAGCGCACGGAAGTCCGCGCTGCGCTGCGTGATCTGGCGGCGGTAGCCGTACGTGAGGGTCGCGCCGCCGCCGGCGGGGTTGACCGCCTGGTCGAAGATGAGCGCGTCGAGGATCGCCGAGCCCTTGCGGAACTCGTCGATGACGGAGACGTCGAGGTCGGTCTGCGCGTTGCGACCGGCCTCGGCGAGGGTGACTGCGGCCATGGGGTGGCCTCCTTACTGTGCGAGCGAGGCCGCGACTGCGGCGTCGAGCGAGAGGGGGGTCTTGCTGGTGGTCTCGCCGGTCCGGCCGGTGAGGTCCGCCCCGCTCTTGCTCGCCGCCTGGACGGTCTTGAGCCGGGGGTTGTCGGTGATGGCCTTCGTGATCGCCGCCGTGATGGCGGTGGCGTCGGCCGGGTCGACGTCCTTGACGGAGTCGAGGAACGCGCGCGAGTCGAGGAGCGCTGCGGGGTCCGCGCCTGCGAGGGTGGCGGCGCGGTAGACGGCGAGCTCGACCTGCGCGGTGCGCGCGGCGGTCTGCTGCTCGGTGAGCTGCGCGGTGAGTGCGGCGGGGTCGGGCGGGGTGTCGCCGTCCTTGACGAGGCCGAGGGCCTTACCAAGGTCCTGCACGAGGGTGTTGCGGGCCTCGGTGGCGGCGTTGGCCTTCGCGGTGGTGCGCGCGGCGCCGGCCTCGGCGCGGAGGTCCTTGACGAGGGTCTGCGCCCAGTCAGGCAGGGACGCGACGTCCTGCGCGGCGTCCGCGCTGGCGGGCCGTGCGGGTGCCTGTGGGGTGATCTGCGCGGCGACGGTCGCCGGGGTGGCCACGGGCGCGGGCGCGCCCTCGGCGGGCGCCTGCGGGGTCGGGGCGGTGGTGGAGTTGGTCTCGCTCACGGGGTGCCTCCAGGGCATGGGTGCGGAATGTCGGTGGTGGTCGGTAGGGTGCGCGGCATCGAGACCGCACGCATTGGGCGGGCGGCACGACGACAGGAGAAGACGATGAATGACGCTCAGGAGAAGGCTCTGGTCGCGGCAGTGGTGACGCTTGGGCAGAGCGCGGCGAAGTCGGCAGCCCCGCATGCGGAGCACTTCGCTACTGCGGCCGCTCGGGTGGCCGAGGCGCATGCCTGGTTGAGCAACCCCAGCCAGTCGCACTGACCTAGATGGCGCGGCCGATCTGCTCACGGCCCCGCTGACGCTTCAGCTCCGGGTGCGCCACCAGGTGCGCCCGGAGCGAAGCCTGCCGCTCCCGCACCAGACGCCCCGCAGCCACCCGCGCACCATCGTCGAGCGCGAGCGCCTCACGACGCTTCGCCTCACGGATGCCACGCTCCAGCGCGCGCTGCTCCTGCTGCGCCACGTACCCGGCAGGGTCCGGCCGCTGCACGCCCGTGCTCGAGACACCCGGCACGTAGATGCCCGTGGAGCACCGACAGTTCGGACCGAACAGGTGCCCAGAGCCACGCACCTCGTCGAGCGTCCCCGCCACCGGCACCCGCCCGCCCGGACCCACAGAGTCGAGCCCAGCGCCGGTCAGCGACAGGATCGCACCAGCCCACACATCGCACGACGGGCACGGACGCGGCCCCGGGATGATCTGCACGAGGTCCTGGCCCGAGGCGACGAGCGTCTGCACGTGCCCGTCGACCATCGCCTGCCCCGCACCGGTGCGCACGGCCATCTCGACGTACGACTCCAGACGCCACGCGCGACCCGCGCGGTCCCGGAAGCCGCCGACGCCGTCGCCGAGGAGCCGGTTCAGGACCTGCTGCGCCGTCTGTCGGCGCGTGCGCGCACCCAGGAGCACGGACCCGAGCTCGGCGGCGACCGCCTGCTGGTAGACGTCGGCGACGGTGCGCAGCACGACCGGCGTCAGCCCGGTCACGGTGCTCGAGACGTCGTGGGCGATCCTGGTGACGGCCGCCCACTGCGCGTCCGGCAGCCGTGGCGCGATCCCGAGGTCGTCGAGGTCGCCGACGGCGAGCGCCTGCCCGAGCGAGTACGCGCGCGAGATCGTCGCGTTGACGACGCGCGCGAGGTCGGCGTCGAGCGCCGCCAGATCCCGCGCGACCTCGGCCCGCAGGAGCGCGAGCTGGGAGAGCTTCGCGGTCTGCCAGCCCGCCGCGTCCCGCCCCTCGCGCAGACGCCGCGCGACGGCGCGCAGGACGGCGACCTCGGCGCCCGCGACGATCTCCACGGCCTCGTACGCGAGGCGCGCGGCAGTGTCGGGGCTGGCAGGCATGGCCTGGGAACCTATGCCCCGTCGATGCCCGGACGGAAGAGCGCCGGGTCAGGGACGGTGTTCTCGGCGCGGATGCGCTCGACTTCCTCGTCGACCTTGGCGGCGTCCCAGTCGGGGTGGAACATGCGGACCTTGAGGTCGGTGGAGATCGCGGATGCCTGGTCGAGGAGCGCGATGGTCTGGGCGACGTCCTCGGGCTCGGCGTTGGCCTTCTCGGGGAACCGCACCTCGGGCACGATCTTCGGGTCGGACTGGTTCGCGCCGAAGACGTGCGCGTCGACGTCGAGCATCGCCGCAGCGAGCGGCCCGAGCGCGGCCTTCCAGTAGCGGATCTTCTTGTCCCGCGTCCGCTCCGAGAGCTGCTGCTTGGACATCACCTGCGTGGCGGTCTCCTGGACGCTCACGGAGTCGTCCCCGAACGACGCCGGCGAGTACCCGGCGCTGCGGAGCGCGACCCTGGTGAGGTCCTGGATGGTGCGCTGGTGCTCCTCCCAGCGGATCGCGAACTGCTGCGCCGTGATCGTTGCGCCGTCCTGCATCGACCCGGTGCCCGCGAGCGTCGTGAACAGCTCCCGCTCGTCGTCGAACGACGCGCCGCTGCCGGGGCCGTTGTTGGTGAGCATCGACTGGTCGACGAACACGCGGGCGCGGGCGAGGCGGATGTCGCGCATCCACGAGGAGTACGCCTCGTCGACGGCGTCGAAGACAGGCTCGATGCCGTCGAAGTCGCTCCGGCCGAGCGGCGAGAGGTCCGGGGTGCGACGCCAGCGCCGCTGGGGGCGGATGTTCGGCACGTACGCGGCCGTGAGCCGCGTCGACCCGGTCGCGATCGCACCCTCAGCGTCGACGAGCTCGGCAGCCCACGCCGTCGCCTCCTGCTCGTCGAGCGGGCGCGCGTGGCCGAGGTCCGTGCTCGTGCCCTGGTACAGGCCGTGCAGGATGCGTCCGGGCTCGTGCCGCTCGAGGTGCCGCCACACGATCTGGCCCTCACGGGCGACGACCGTCCAGAACGTCACGCCGACGAGCATGCCGTGCCGCCACTCCGGGATCGCGCCGTCCGCGGCGACCGACCCGAGCAGCGGATGGTCGGCGACGTCGGTGTCCCACGTGATGCGCAGGTACGTGCCGCCGTGTGCGGCCGCGACCTCCGCGGCTTCGAGCAGCCCGGCGTGGACCAGCGGCGTGTTCATGATCTCTTCGAGGCGAGCCTGCGCCGCGTGGTCGTTGTCGCCCTCGTCCTTGGGCAGGAGGATGCGCGGCGGCTCCGAGAAGAGGAGGTCCGCCGAGGTGGTGGCGATGTCGGCCGGCAGCGGCACGTGCAGGCGCGTGCGCGACTGACCCTCCGGGATCGGCCGACCCCAGAAGAACCGCGCCACAACGCCGACGACGCCGCCAGAGTGCTGCGAGGAACGCACGCGTGCCGCGGCCCGCGTGCCGCCGTAGACGCCTGCGAGGCGGGTCGTGTCGCCGACGTACCAGGCGTCGTGCTCGTTGATGAGGGCGAGTGCCGTGTCGAACGGCTTCGGTGGCCAGACGCTGCCGGAGGCGGGGAGAGCCATGCGAGGGTGCCTCCTGTCAGGCTGCGAGTCGGTGGTGCCAGTAGCGCTCGGAGGAGACGACCGCGTAGCGCAGGGCGTCCAGGCCGTGGTCGGCGACCTTGATGGGCTTGTCTTCGCCCTTCTCGGTCGCCTTCGGGTCCCAGGAATACCCGGGCGCTTCGGCGATGAGGTGCGGGCAGCGGTCGGTGACGACGAGTCGGTTGCGGCCGAGGAGGTTCGCGACGGTGCGGATGCCGTACGCGACTTCGTTCGAGGCGGCGGTGAGGCCGGTGACGCCGTCGGATCGCAGCTGCGTGTGGAAGGACGCGGCGGCGGGGTCGAGGAACGTCCAGCGGGGCTGGAGGTGCAGGGTGTCGCGCAGGTCGTCGGTCCAGGCGCGCAGGCCTGCGGAGAGTTGCGCGTCGGTCCAGCGGTGGCCCTTGTCGCCGGCCTTGTACCGCCACTCGTCGACGACGACCAGGCGCTGAACCTTCTCGGCGGTGATGCCGAGCGCGACGGCGTGGGTCGGGTTCGTGGTGCCGTAGTCGACGCCGACGGCGATGAGCTCGGCTAGCGGCGGCAGGGTGTCGTAGGCGATGACGTGGGCTTGCGGGTCCCACATGTCGTAGATCGCGCCTTCGGCGGCGACCCACTCACCTTGGATGAACCGCCTGTACCAGAGGCCTGTGAACTCGGCCTTGATCGAGGCCTTGTACTGCTCGGACAGGGACGGGTTGTCGTCGAGCGTGAAGTGCCAGGACCGCCAGTCCAGCAGGTCGCCGAGGCGGTCGAGGAACTTCGCCTTGAGCCAGTGCGCGGGGCTGTCCGGGTTCGTCGTGCCGAAGAGCTGCGCGCCGCGGACGCTCATGCGGCCGAGGAGCTGGGTGAAGAACTCTTCGGGGATGACGGTGATCTCGTCGACGTAGGCGCCGGCGACGGTCATGCCTCGGATGATCTTCTCGGCCTTGGCGTCGGAGGCGCCGATGACGTGGACGGTGCGGCCGAGGATCGTCGCCGAGGGTGCGCCGTTGGTGTAGACGACGAGTGCGGCCAGGGCGCCGAACAGGCTGGGGTCCTGGAGGGGCTTGATGACGTTGCGGAAGAGGGCGTCGCGGGTGCGGCCGATCATGATGAGTTCGCCGCCGCGCGGCGCGCGGGCGATGAAGATCAGCCAGCGGAGCAGGGAGACGATGGTCTTGCCGGACCGGATCGTGCCCTCGAGGACGTTCACGCGCGCCGAGGACTCGCGCATGAACGCGAGTTGCTTCGGCGACAGGCCCGCCTCGACGGTCGTCACGCGACGCTTCCCGGCTCGGGGACGCCGATCGCGTCGGCCAGGCGCTGGAGCATGCTGAGGGCCTCGTGCGTGCCGCCGTCGGAGTCGTGCTGGGCGATCTTCAGCGACCGGTCGATGGCCTGCGTCGCCGCGGACATGAGCTTGAGCTTGTCCGTCGGCGTCGGCTCGTCCTGCTGCCAGCGGACTTCGATGTAGTCCTTGCCGCCGTGGTCGATGTACTCGTGCGGCTCCCACATCTGCGCGCGGAGGCGTTCGGCGTCGTCGAGGAGCTTGTGCTCGAGGAGGGCTCGGCGGGCCTTGGCGTCGATGACGACGGCGCGGGTGGCGGCGGCGGTCTGCGCGCGGTCCCAGCGGAGGCCGGCCTTGCGGGCGCGGTCGGCGACGCGGGTCTTGGTCATGCCCATGCGCTCGGCGATGTGGCGGACGGAGAGGCCCTGTGCGTGGAGTGCCGCGAGCTGGGTGTCGTGGTCGGGGGTCCAGGGGGCGATGGTGGCCAC

Protein sequences of DBSCAN-SWA_2

>NZ_CP049862|1009662:1023981|1022224_1023439_-|WP_166415199.1|terminase|DBSCAN-SWA
MRESSARVNVLEGTIRSGKTIVSLLRWLIFIARAPRGGELIMIGRTRDALFRNVIKPLQDPSLFGALAALVVYTNGAPSATILGRTVHVIGASDAKAEKIIRGMTVAGAYVDEITVIPEEFFTQLLGRMSVRGAQLFGTTNPDSPAHWLKAKFLDRLGDLLDWRSWHFTLDDNPSLSEQYKASIKAEFTGLWYRRFIQGEWVAAEGAIYDMWDPQAHVIAYDTLPPLAELIAVGVDYGTTNPTHAVALGITAEKVQRLVVVDEWRYKAGDKGHRWTDAQLSAGLRAWTDDLRDTLHLQPRWTFLDPAAASFHTQLRSDGVTGLTAASNEVAYGIRTVANLLGRNRLVVTDRCPHLIAEAPGYSWDPKATEKGEDKPIKVADHGLDALRYAVVSSERYWHHRLAA
>NZ_CP049862|1009662:1023981|1023480_1023981_-|WP_166413357.1|DBSCAN-SWA
MATIAPWTPDHDTQLAALHAQGLSVRHIAERMGMTKTRVADRARKAGLRWDRAQTAAATRAVVIDAKARRALLEHKLLDDAERLRAQMWEPHEYIDHGGKDYIEVRWQQDEPTPTDKLKLMSAATQAIDRSLKIAQHDSDGGTHEALSMLQRLADAIGVPEPGSVA
>NZ_CP049862|1009662:1023981|1019406_1019565_+|WP_166413354.1|DBSCAN-SWA
MNDAQEKALVAAVVTLGQSAAKSAAPHAEHFATAAARVAEAHAWLSNPSQSH
>NZ_CP049862|1009662:1023981|1009662_1014009_-|WP_166413344.1|tail|DBSCAN-SWA
MSLTVGELVAYIKVDDQDSARKLDGVAQGMGKVQAAADKAARAGESLVAAQHAVARSADAVAKAEKALADARKSGDQEKVAAAEKSLQQARERQAVSASKLERAERNVRSATEASAAATEASAEASKKATIASRLQSEAAQDLANRTALVGGALTAAAGIAVKFFADFDEGMSGVAATGDDARQNIDGLRASAIQAGADTKYSATEAAGGIEELAKSGVTAKDVLAGGLKGSLDLAAAGNLGVAEAAEYAAIAMTQFKLKGSDVGHVADLLAAGAGKAMGEVSDLGQALKQGGLVASATGLSIEETTAALAAFAAGGLLGSDAGTSLKTMLQRLSAPMGDAKQLMDSLGISAYDVSGQWVGLEQLAGQLTNALGDMTPAQRNAAMATMFGADAVRAANALYENGADGVREWTAAVNDQGYASEVAAIRMDNLKGDLETLSGSIETVFIQAGGGANDVLREMAQGAGALVDAIGEVPGPVLEVLTVLTGAGGMTALGVAGLTKLVGGLKNAKNAAEGLKLSAKGASVAVGAVSAAIGVATIGVMAWANAQAESKQRIDSLRESLDGVTGAVTESTRQVIAAELVKTPDWWTFDFSGSAAEGAEALGISVETVTNAILGQKDAMAALERYYGPQEVAYGNIREEAEKNGLSIGDYNDAVGALRRGLQGQSKDLDAAKKKHELMAEATGATSEETDRAAKSVELFATNLEDQAKAADAAWKAIKGLADGVLGMRDAERGYEAALDAVNESLKKNGQTLDVGTEKGRANQAVLDGIADAGWKWIDQMRAQGATDEQLQKKMGRTRREFVDAAKQMGLSEKAAKKLADELGLIPSNIKTEVDVDTSKASAEVTRFIREQMKRQIAINVVTNSGGGGKTHVQAKATGGAVVGPGTGTSDDILARLSNGEHVITAREVAAMGGHAQVTKWRAAALAGRALPAFAAGGRVGANDPVVDATAAVKRARSAVKREERQVESALNRWRDIPGDKKNRDRKRTAQRQLDDERKDLKAAKAALKNAEKALDDARKERAEEREKQSRLSDARADLAVDARRGNITDQVSSGLSGAYSVVDTLRDQSKNSDLSKAQRANLAKTAREAEVALRKLYAQAEGIEKKLDTARDHTQQLASIKASVAGVLAGEFKLSDSLGKKDAYGYDQPVTAKGLLASAQKKAGDLKTFGGKLDKLAAAGVAGVILQEIAHEGLEGGTALADALLADPSTIKALNGAYADIDRYSQAAGASATKNTTIDGRFYRGGVEAAEAIVDGLEDQLGSVTASIEAWGVTMENALLASLGLKRDSKGNIVKASANSSPIAVGPDPGASGDIRAPRTVAVGPDPGASGDIRAPRAVTAQDVAARGGDGRAGGLRRTALNGNLPGLRNGGPVAANMPVAAPINAPTPAPVYVTIPDIYVRNPITGEDVKVLTRQVVRAEMRTPTTAMAVTRLGQNELRRVGEN
>NZ_CP049862|1009662:1023981|1014333_1014726_-|WP_166413345.1|DBSCAN-SWA
MAKSFTRYLRPNLDLEARDGKIYHVPPPTKHNGLVLAAIVAYGMNKATGRETDDETMALWESIPGDTPVGHLALTQAVYDQMLADGQPEIDVDRYALYAQYYWTLGEDAADQVMEFTYGPADDEGAAPKA
>NZ_CP049862|1009662:1023981|1016063_1016414_-|WP_166413348.1|DBSCAN-SWA
MAMRSTLTLNLGATKAALRTAAAAGLKVGAEVVLAESRKVVPIEEATLSRSGATDVDEATLTASVSYDTPYAVRQHEELDYRHDEGRQAKYLEGPLLEHRDQALAAIAQTIRGRLA
>NZ_CP049862|1009662:1023981|1014803_1015556_-|WP_166413346.1|DBSCAN-SWA
MSVPTDLGLSYELDLDINLAGPGVTPAIWQQIRFTSAINPQHAPTLVDAATYDDEGAQNQAKLGESANLAFTIQSQRNPDGSFLPEVQALLNAAKPGTRGNAALAEVRVYDSLGADYAFQGIYSVQMDRGNTGNADLGGWSATLTGKGKIKPIANPAPAGGSPSAPPVLGSAAPSAAAAGDIVTIKGSGFAGVLLATAVKVGATSATSISVVGDSTIVAVVPAGSAGSAPITVTHPTNGASNALPYTRGA
>NZ_CP049862|1009662:1023981|1020660_1022208_-|WP_166413356.1|DBSCAN-SWA
MALPASGSVWPPKPFDTALALINEHDAWYVGDTTRLAGVYGGTRAAARVRSSQHSGGVVGVVARFFWGRPIPEGQSRTRLHVPLPADIATTSADLLFSEPPRILLPKDEGDNDHAAQARLEEIMNTPLVHAGLLEAAEVAAAHGGTYLRITWDTDVADHPLLGSVAADGAIPEWRHGMLVGVTFWTVVAREGQIVWRHLERHEPGRILHGLYQGTSTDLGHARPLDEQEATAWAAELVDAEGAIATGSTRLTAAYVPNIRPQRRWRRTPDLSPLGRSDFDGIEPVFDAVDEAYSSWMRDIRLARARVFVDQSMLTNNGPGSGASFDDERELFTTLAGTGSMQDGATITAQQFAIRWEEHQRTIQDLTRVALRSAGYSPASFGDDSVSVQETATQVMSKQQLSERTRDKKIRYWKAALGPLAAAMLDVDAHVFGANQSDPKIVPEVRFPEKANAEPEDVAQTIALLDQASAISTDLKVRMFHPDWDAAKVDEEVERIRAENTVPDPALFRPGIDGA
>NZ_CP049862|1009662:1023981|1019566_1020649_-|WP_166413355.1|DBSCAN-SWA
MPASPDTAARLAYEAVEIVAGAEVAVLRAVARRLREGRDAAGWQTAKLSQLALLRAEVARDLAALDADLARVVNATISRAYSLGQALAVGDLDDLGIAPRLPDAQWAAVTRIAHDVSSTVTGLTPVVLRTVADVYQQAVAAELGSVLLGARTRRQTAQQVLNRLLGDGVGGFRDRAGRAWRLESYVEMAVRTGAGQAMVDGHVQTLVASGQDLVQIIPGPRPCPSCDVWAGAILSLTGAGLDSVGPGGRVPVAGTLDEVRGSGHLFGPNCRCSTGIYVPGVSSTGVQRPDPAGYVAQQEQRALERGIREAKRREALALDDGARVAAGRLVRERQASLRAHLVAHPELKRQRGREQIGRAI
>NZ_CP049862|1009662:1023981|1016425_1016740_-|WP_166413349.1|DBSCAN-SWA
MKLPRILTPHTVTVRNAEGTGAYGTVLGPDRTLEHVRVEETTRLVRDRNGQEVVSSARVFLRPEHGPVPLDSEVDLPSGRTAVVLAVAHHHTPPAPEHNELSLT
>NZ_CP049862|1009662:1023981|1018647_1019301_-|WP_166413353.1|DBSCAN-SWA
MSETNSTTAPTPQAPAEGAPAPVATPATVAAQITPQAPARPASADAAQDVASLPDWAQTLVKDLRAEAGAARTTAKANAATEARNTLVQDLGKALGLVKDGDTPPDPAALTAQLTEQQTAARTAQVELAVYRAATLAGADPAALLDSRAFLDSVKDVDPADATAITAAITKAITDNPRLKTVQAASKSGADLTGRTGETTSKTPLSLDAAVAASLAQ
>NZ_CP049862|1009662:1023981|1015647_1016067_-|WP_166413347.1|DBSCAN-SWA
MTVPATSLYTALAERLHAAGVATWNPAGIYTPGQTGITLTVMPAAPDRAVVLTVYDRDEHADPRLTDERVRVQVRVRAAKGRPDSADALAEAVHAVLRAHHVTWSGVAITRVHRRSYLPLGLDSNGRPEVSMNYEVLLP
>NZ_CP049862|1009662:1023981|1016736_1017141_-|WP_166413350.1|DBSCAN-SWA
MRTYATLADVNGSPWRLGLSAEAAEDLIALASADVERLTMTAVYEVDTDGLPTDPVVRAALRDATCATVAWLDETGDTSGAAARYNSLSLGSFSVSGGGVGSGTNTDAAASLVAPRAITILQNAGLIGRAPRTP
>NZ_CP049862|1009662:1023981|1017349_1017628_-|WP_166413351.1|DBSCAN-SWA
MAARKAQDAPAPEAPEVVTPEAEVVTPEVTDPEVPTTEPADAEPVEVEVHSPATDFTGDVLGVTFTKGTAHTSDPVALAYFTRRGYTVAPEA
>NZ_CP049862|1009662:1023981|1017630_1018635_-|WP_166413352.1|capsid|DBSCAN-SWA
MAAVTLAEAGRNAQTDLDVSVIDEFRKGSAILDALIFDQAVNPAGGGATLTYGYRRQITQRSADFRALNSEYTTAEVTTEHKTVSLVPLGGAFEVDRVIAKIGPAASGSVALNLKNTITATTTRFQDEVINGDVAVDAKGFDGLDKALTGSATEFRATSVTDWTDFDTDSRAEHKALDAIDEFLALLDGSPTVLLGNAKALARVRAAARRAGMYTKNPVEGLLGPNGRPITREAYGDVIFADPGAKAGSNNPIIPIENRTVGTAQTGLTDLYAIRVGLDGFHAVATVGGQLVETWMPDFSTAGAVKKGEVEMGPVAVALKATKAAAVFRNIKVA

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_166413344.1|1009662_1014009_-|tail	phage tail tape measure protein	I3NL90	Bifidobacterium_phage	1.6e-68	46.8
WP_166413345.1|1014333_1014726_-	hypothetical protein	NA	NA	NA	NA
WP_166413346.1|1014803_1015556_-	hypothetical protein	A0A0U4JQQ8	Arthrobacter_phage	3.4e-11	58.3
WP_166413347.1|1015647_1016067_-	hypothetical protein	NA	NA	NA	NA
WP_166413348.1|1016063_1016414_-	hypothetical protein	A0A1V0E617	Streptomyces_phage	1.6e-24	56.5
WP_166413349.1|1016425_1016740_-	hypothetical protein	NA	NA	NA	NA
WP_166413350.1|1016736_1017141_-	hypothetical protein	A0A1J0MC98	Streptomyces_phage	5.5e-16	45.5
WP_166413351.1|1017349_1017628_-	hypothetical protein	NA	NA	NA	NA
WP_166413352.1|1017630_1018635_-|capsid	phage capsid protein	G9FH86	Rhodococcus_phage	1.1e-134	74.7
WP_166413353.1|1018647_1019301_-	hypothetical protein	NA	NA	NA	NA
WP_166413354.1|1019406_1019565_+	hypothetical protein	NA	NA	NA	NA
WP_166413355.1|1019566_1020649_-	hypothetical protein	A0A1J0MCY1	Streptomyces_phage	1.9e-55	39.2
WP_166413356.1|1020660_1022208_-	hypothetical protein	A0A1J0MCN7	Streptomyces_phage	5.3e-99	42.9
WP_166415199.1|1022224_1023439_-|terminase	PBSX family phage terminase large subunit	A0A1J0MCH4	Streptomyces_phage	1.5e-117	54.7
WP_166413357.1|1023480_1023981_-	helix-turn-helix domain-containing protein	A0A1J0MCI5	Streptomyces_phage	1.4e-13	37.8

Sequences of DBSCAN-SWA_3

Nucleotide sequences of DBSCAN-SWA_3

>NZ_CP049862|1084296:1102554|DBSCAN-SWA
ATCATCGGACACCTTCCAGGAGGTCCGCCGTGACGGCGGGGTAGATCTGGTCGCGTGCGACGCGCACAGTGGCGCGGACGTGGGCAGGAATCTCGTCGAGCACGAGGCCGAGCAGCGAGCGCGGGTCGAGACCGCCGGTCGACGGCAGCTCGACCTCGAGCCAGGCCGTGTCGGCGGGGCACGCACCCTCGGCGAACACGCCGCCGCCCTCGCGGACGACGACGCCCGGCCCGCACAGGGCCGTGAGCACGGTGCGCAGCGCGCCCGGCGTGCCGCGCGACATGAGCGTCGCCGCCCACGCCTCGAGCAGGGCACGCTGCCTCGCCTCACCTGGCACCTCGGGGCTGCCCCCGTCACCGGCGCCGTCGGACGGTGCGTCACTGCCTGACGTCACCCCCGCCCCGCCGTCGAGCGCCCGCACCCCGATCCACGACGCGAGCCACGGCAGCATCTCCGCGGGCGTGAGTCGGGTGTCGGCGAGGACGTCGAGGTTGTCGCCGTGCGCCTGCAGCGTGTCGGCCTGCTCCTCGAAGATCGTCACGAAGCGTCGGAAGAAGTCCTCGTCGACCATCGCGGGCGGCAGCTGGTCGACGAGCCACCCGGGCCGGCGGCTCATCGCACGACCACGCGGTGCGCGGCCGAGACGAACAGGGCCCCGGGCGTGAGGGTGAGCGCGTCCTGGCTGTCGCCCAGGCGGCGTCGGCCACGCAGGTCGTAGTCGAAGAGCGTGACCTCCTCGACGCGCTCGACGCCGTCGACCTCGTCGACGACGTGCGCGAGCGCGGCGGACGTGAGGTCCTCGCCGAACGGCCAGCCCGCGCCGTCGGTGCCTCCGTGGAGGGGGTCGACGAACCGGTGGATGGCCTCGAGGACGCGCTGGCGCACGACGGCCGCGGGCCGCCCCGGCAGGGCGCGCACGAGCACGGCGGCGCTCGCCCCCTGGTAGAAGGGCGCCCCGACCTCGAGGCCCACGCCGACGAGCCGGCACGCGTCGAGCTCCGCGCCGACCCGGGCCCGCAGCTCGGGGGAGAGGGCGAGGTCGTCGATGTCGCGGTCCTCCGCGGCGCCGCGCGGGGCCGCTGCGGGCACGAGCAGCACGCGCACCGCGCCCGCCCTGCCCGCCACGGCGTCGCCGAGGGGCAGGCAGCGTGCGCGCGCGACCGCGGGCGACGCGGCGAGCGCGAGGCGTTCGTAGTCGCCGGCCGTCACGGCTCGGCGGCCCGTGCGCAGCGTGAGCGGCCCGCGGACCTTCGCCTCCTCGACGGTCTCGGGGTCGACGCCTCCGGACGCGGCCGTCGTGTTGGCGACGGACGCGACCATCGGCAGCGTCGTGCGGGGCGTGACGAGCGTCCCGGGCCCGACGTTGCCGCGCGCCCCGCCGCCCGAGCGGTAGGGGCTCACGCGCACCTGGGCGCCGTCGGCGGGGATCGCACCGTGCTGGCGTACGCGACCGTCAGGGTGGCGGACGGACGGGCCGAAGCGGACCTCGCCCGTCGCGGAGTCCCACACGACGTGGCGGTCGGTGGGGCCGGAGGCAGCGAAGTCGGCGACCTCGGTCCACGGCTCGGCGTCGCTCGTCGTGACGACGAGGATCTCCTCGCTCGGGCGGCGCGCGAGAACAGGCGTGTGGGCGACGCGGAAGACCTGCCCGGCCGTGCCCGTCGAGCGTCCGAGCACCTCGCCCGGGCGCCCCGTGACGTGCTCGGCGGGGACGGTGACGCCGACGACGCCGACGTCGAGCGACGTGAGCCGCGGCGACGTGCGGTACGTCGGCCGGCCGGGCGCAGCGCGCACGAGTCGCACGCGCACCCAGTGCGCGCCCGTGCCTCCGAGCGTGAGCGGCGGGTGCGAGCCCGGCAGCAGGAGGACGACGCGGCCGTCACGGTTGAGCCCGCCCGTCGTGTCCTCGTGCACCGTGAGCCGCACCCACGCCTCGCCGTCCCACGCCTCCCACACGAGCGGCGGGTCGGTCGGGTCGATGCCGATGCCGAGGACGTCGGCCGCGACCGTGAGCTCGAGCGCGTGGTCCGCGAGCGAACCGGTGAAGCCCAGGTACGTCGCGTCGTCGAGCGTGATCTCCGGCGACGGGAACACCGCGAGGCTCGTGCCCCGGTAGGCGAGGTCGGCCCAGCCGTCGACGAGCTGGTCCGAGCCTGCCGCGGACGTCATCACGGCGCGCAGCGACGCGGGCCGCGCGACGGCCTCGCGCACCGTCGTGAAGACGACGTCGTCGGACGCGGAGCCCGACGCGGCGGGCGACGTCGCGACCTCGACCCCTGCGGGCACGACGACCTCGGCGCGCGCGGGCGCCGAGAACCAGAACGTGAGGTCGGCGCTCGCCGCCGACGGCCCGAACGGCTCGATGCCGACGAGCCCGAGGAAGTGCGCGTACATGCGCTCGGGCACCTGGTTGACGCGGAAGAGCACCATCTCGCTCATCCACGCGAAGAGCTCGACGAGCGCGACGCCCGGGTCGGAGACGTTGTGGTTCGTCCACTCGGGGGTGTGGCGGGGGATGAGCCGCTTCGTCTCGTCGACGATGTCCTGGAAGGACCGGTCGTCGAGGTTCGGCGGGATGATCGGCGGCATCAGGATTCCTCGTGCGGGATGACGTAGAAGGGGTGGACGAGGTTGCGGCGGTCGTTGGTCGCCTTGACCCGGTAGGTGAGGTCGATGAGGACGAGCCCGGGGTTGTCGTCGTCCTGGCGGGGCGTGACGTCGAGGACCTCGATGCGCGGCTCCCACTGTGCGAGCGCGTCGCGCACCGCGCGGTCGACGAGCCCGAGGAGGTTCGCGGTGACGGGCTCGAAGAGCAGGTCCCAGATGCGGCAGCCGAACTGCGGTCGCATGAGGCGCTCGCCGGGCGCCGTGAGCAGGACGACGCGGATCGCGTCGTCGAGGTCGCCCGAGCCGTCCGTGAGCGCGATCGAGCCCGACGCGTCGACGCGCAACGGCCACGTGAAGCCGCGTCCTACGAAGGACGCGGCGGAGGATGCGTTCTCCATCAGTTGATCTGCACCATGCCTCCCTTGACCTGGGTGACGCCGCCCGCTTCGAGCGCGGCCTTCGCCTGCCCCTTGACCGACACGTCAGCACCTTCGAGCGCGAGCTTGCCCTTGGCCCTCACGCTGATCTCGGCGGCCTCGAGCGCGAGCCTCTGCTGCGCGCGGACCGTGATCTCCGTGCCCTCGACGGTGACGGAGCCGTCGTCGCCGACGACGATGCGCGTCGCGCCCGCCTGGATCTTCACGGGCCTGCCCTTCGGCACTGTGAGGTCGACCGCGTCGCCGCCGAGTCGCAGGCGGGTCTCGCCTCCGGGCAGCGCGAGCAGCACGTGGTCCTTGGCGGCGCTGTCGCCGTCGACGAGCTCGAGGAGGTTGCCCCGGCGTGACGTGAACGCGCGACGGCTCACGGTCGATCCCTCGACGGGGTACGTCCCGGGCGCCTTGCGGCGCTCGGAGTGCAGGCCCGTGACGACGACGGGTCGGCGCACGTCGGAGCCCTCGAACGCGACGAGCACCTCGTCGCCGACCTCGGGCACGACGAGCAGGCCGCGGCCCTCGCCCCCGCCCGCGGACGCGACGCGCGCCCAGTCGGACGTGATCGTCCGGCCGAGGAACGGGAACTCGACCTTGACGCGGCCCGCGCCGCGCGCGTCGTTCTGCGCGCCGAGCGCGGTGACGATGCCGACGACGACGCCGTCGTGCGTGTACGCGGCCGCACCGCGGTCACCTGCCCGGCCGCCGAGGTCGGCGAGCGTCGTCCGTGCGCGCGAGCCCGTGACGACCTCGGTCGACCAGCCTGCGCGGTCCCACGTCGTCGTCACCTCCCGCACGTACTCGGCGTCGTCGGGCCACCACGTGTGCTGGAGCGTGAGGCGCGACCCGGGCGCGAGCGGCACGAGACGGCGCACGAGCGCGCGTGCCGCCACGGGACCGGACCCGGCCAGGCGGGCCCGGGCGATCCGGGTCGCCTCGTCCGCGTCGAGCGGGAAGGACGTGGAGTCGAGGACGACGCGCTCGCTCACCGCGATCCCGTCGACGGCCTTGCGCTCGTGCTCGCCCGTGACGGCCGCGCCGGCCTCGGGGTCCCACGACGTGACGACGGCGCGCGTCGGGCCGCCAGACTCCTGGGAGACCTCGCACGTCGCGACCTCGTCGGCGCGGAGCGTGACGTGCTCCGCGCCGGGCCGTGGCGTGCTCGCCGGCCACAGTCGCAGGGTCGTGCCGTCGAGCATCCAGTCGCTCCCGGTGCGCTGCGCGACGTCGTCGACGAAGCGCAGGGCGGAGCCCGCCTGGAGCATGTAGTGGACCTTCGCGGGCGGCAGCCCTGTCGCGTCGACGCGGAGGCCGGCCGACTGCACGATCTTGCCGAGGATCGACGCGAGCCCCTCGTCGACGAACGTCTGCGCGGTCTCGGACGCGAGCAGCGCCGTGGCGTCCTGCGCCGTGACGACGAGGCGGGTGCCGCCGCGCTCGCCGCGGACCGACTCGATGCGGGTGACTGTGCCCTCGAAGACCGTCGCGACGACGGGCCGGTCGCTCGGACGTCCGCCGACGGTGACCTTCTGCCCGACCTTGACGGCTCCGATCCCGCGCGTGGGGTCGAGGACGTGCGCGGAGTCGTCGACCGCGAGCTCGAGCCGCGCCCATGCCGTCGTCCGCAGGGGCCGCACGACGCGCAGCGCGACGAGCGTGCCCGTGAGCGACGTCGGCAGCGGGCCGCCGTCGAGAGTGATGCGCGGAACGAGCGAGACGCCTGCCGCTGCGGACGTCACAGGTCCTCGATCCCGGGCACGGCGAGCAACGTGCCCGGCACGAGCCGCAGCGGGTCGGTCACGGCGTTCGCGGCCGCGAGCGGCCGCCAGCGGGTCGCGTCGCCATAGTAGCGGGCCGCGATGCGGTCGAGCGTCTCGCCCGACTGCACGCGGTGGACCCGGTGCGGCTGCGGCGTGCCCGACGTCGGGTTCTGCGGGCCGAACGCGTGCTCGGGCTCGAACTGCTGCAGGACGAGGTCGAGGGTCGCGCGCAGCGGCGTGCCCGTCGGCGAGAAGTACGTGTAGGCGAGCGCGAGGTCCGCGATGACGGAGCGGAACGAGTGCACCTCGCCCCAGTGGAAGGTCACGAGCGGCGGCCGCACGTCGCCCGCACGCTCGTCCGAGCCGGGAAGCGTCGGGTCGATGTCCATCGCCTCGACCACACGCCCGGTGTGCTCGGCGACCGAGCGGCCGGTCGCCGTCGTGTCGAAGAACAGCGACACCTCGAGGACACCGGGGCGCGCGCCGCCGAAGCGCAGGCGCGGCGTCGGCCGGCCCGGACGTGGCGTCGCGTCCCACGAGTTCGAGCGCGTGAGCCGCAGCTCGGCCGGGTTGTACAGGCACGGGATGCGCTCGCCGCCCTCGAGCTCGAGGAACGCCTTCTCGGGTGCAGCCATCAGAACGCTCCAGGGGTGAGGCCGGTCGTACGCAGCGCGGACTCCTCGAGCAGCCGACGCTCGACGCGCCGCGCGACGCGGTCGGTGAGGTCGTCCTCGAGCGCGTCGGCGAGCCGCGCGAGGAGTCGCTCGTCGAGGTGGAGCTCGCCCGCGCTCGCGCGGGCGGCCCCGGTCGTCGGGAGGGTGCTCATCGTGGGCTCCTCGCTGCTCGGGGAGAGGGCGGAGTCGGCGCGCGCGAGGGCGCGCCGCAGGATCGAGAGGCCGGCCGCGGTGTCGTCGTGGGACGCGCCGAGGCGGGCGACGGCAGGCACGGCCGGCGCGCCGGGAACCGGGGCCGCGACGCGCGCGGGCGCGCGCGGCGGCAGGACCGAGCGGCGCAGCGGCACGGTGGCCGCGTCCGTGAGGGACGATCGCCAGGCGCTCGCGGTCGCGGGGGCAGCCGGGCCGCGCTGCGCGGGGCGACCCGCGACGGGCGGCGTCGCGCGTCCGGCGAGGCTCGTGCCGCTGTGGTGGGCGGGGTCGGTCCCCGCCGTGCGGCCGGGGCCGGACGGCGTGCGGCGGACCGCGGGTGCGTGGCGCCACGGGTGCGTCGACGCCGCTGCGCGCGTCGCGCCGTCGTGCGCGGGTGAGCCGCCGACGGCGAGAGGTGTCGTCGGTCCGGTCGCGCGCCGCACGGCGCGCGCACCTGCGCCGAGACGCACGTCGGACGCGGGGGAGGTGAGGACGGCCGACGATCGTGCTGCCGACGTGCTTCCCGACGACGACACGGACCGCGTCGCGTGCCCGACCGCCTCGGAGCGGGCCGCTGCCGTGCTGAGCGGGATCCCCGGAGCGCGCACGCTTCCCGCCGGAACGCCGGAGGGCGACCCGAGACCTGTGGCGCCGCCCGCCGACGACGGCAGCACCGCCGACGCGACGTCGAGCCCGCCGGGTGCGGCGCCGGTGGTGCTGACCGACGACGCGGCACCTGCCGCACGAGCAGTCACGACGCCGCGGGACGACGGCGCGCCGGGCGTCGCGGACGTGGTTCCGCCGGTGAGAGCGAGGGTCGCGGCGGACCGTGCGGCCGCGTCGTCCCGGCGCGTGACGGCGACCTGACGGCGCACTGCGGTGACCTTGCCCGGCTGCGCAGCGGCGACGCCTGCGCCGCGGACGTCTGCCCGGCGCGCGAGCATCCCGGGCACCGGTCGGACCACGCGGGCGACGGCGTGGTCGCCGTCCCGGGCGGGGCCGGTGAGCGTGGGCGCGGCTGTCCCGTCGGTCGGGTCGGCCGCGCGTGCGGCGGACGTGCCGGTGGACGTCCGCCCGTCTGGCGCACCGACGCGCGCGCGGGCCGACGCGCTCTGCGCGGCGAGGCTCCCGGGCACGGCGAGCGCGCGCCGCAACGGGACGTGCGACATGGTGAGGTGCGACGGGGTGACGTGCGACGTGGCGGCTTGCGGCCCGGCGGTCAGGCCCGCGGTCGGTGCGGGAGTGGCCGCGTCGGTCGTCGGCGAAGGCCCCCGCGAGGTGGGGCCGGCGCCGGACGTGCTGGCGGTGCTCGTCCCGCCCGCGGAGGCCGGGGTCGCATCGGTGCCGGTCGTCGGGCGGCCGGTGGTGGACGGGTGCGTCGTCGAGGGTGCGGCAGTCGTCGTGCCGGAGGTGCCCGGGCCAGCCGACGAGACGTGCGGGCTGGCTGCGGGCGCTGGTGACGCCGTCGCGCGGCGCACATCGGCGACGGCCCCGCGCGACCCCGGGTGGGCGGCCGGGACGTGACCGGCGTCGGCCTGTGCCGGGCGGACGAGGGCTGTCGGGCGGAGCGTCAGCGCGCCGGTGCGTGCGCCGGCGACGGCGCGCTGGCCCGACGCCGTCGATCGGCGCAGCGCGGGCGCCGAACGAGTGACGGCCGAGGCCTCGGGGGCGTGGCCGAGCAGCGAGCGTGAGCTTGCGGCACGGGGGAGCGACGCGGACCACGTGCCCGGGTGGCGCTCGGCGGAGGCTCGTCGCACCTCGGGCGAGGTGGGCAGCTCGTGCACGGACGCGGCGGGTGCGGGCGCGTCGGGCACCATCTCGGTGTGCCGTGCGGAACTGTCGCGCGTCGACGACCGGTCCGCCGTCGGGCTCGACGCCGCGACGTTCGACGCCGCGACGCCGGACGCCGCGACGCCGGTCGTCGGACGCGTCGCCGCGGACGAGCCGGGCAGCATGGCGGAGCCGGCGAGCGTGGCCCGAGCCGCCGCGGCCGTGCGCGACGCAGCGGCTCGCCGTCGGGCGAGGCGTGGCGGAGCGGTGCGGCGTCGGACCGCGGGGAGCGCGGGCGCGCCCGCAGCTCGCGGTGCGGGAGCACCGGGCGGGGTCTGGGTGGCAGCGGGTCCGGCGGCACGGCGCGACCCCGCGGCGCCGTCCGTGGGTCCGGACCCGGTGGGCCGGGGGGCGGGCCCCCGGGAGGGTGCGACGCTGCGGCGCCGCGAGTCGAGGGACGTCACCATGGAGCCGGCGGCCGCGACCTCGGCGGGCAGGCGCATGGGAACCGCCTTGGGCGTCGCGCTCACGCCGAGGCGGCCAGGCGTCCAGGAGTCCCGGTCGATGCGCGACGCGGCCCGGGCAAGTCCGCGCGGCGGCGCGGCGACCGGCGTGCGTGACGGACGCTGCGCGTCGTCGTCGGCCGGGGCGTCGGGCGCCGGCGACCACCAGCGGGGGGCGCGCACCGAGCGTGCCGCGGGCGGGGCGCCGACCTCGGTGGTCTCGCGCAGAGCCGTCGTGAGCGGCGCCGGGCGCCGCACCGCGGGCGTGCGGGCGAGGCCGCGCGCGAACGCGGCCGAGCCCGCCGCGGTGAGCCCGAGGCGACCCGCGCGGAAGCGCGTGAGCGCACCTGCGGGCCGCAGGTGCGCGGGGCCCTGCGGCTGGTCGGGCGCGGTGGGCCCGGGCGGGAGGGTGGGGATGCTCATGACGTCTTCGCCCGGAAGCCCTCGTGGGAGACCTCGAGCCGCTCGACGAGCGTCGCGTTCGACTCGACGTCGAAGGTCGGGCCGTCCCACGCGACGGCGAACACGCCGTCGACGTCCCACGCGCGCAGCCGCTCACCGGTGTAGTCGAGCGCCGTCACGGCGCCCGTCGACCGCACGAGCTTGCCGCCGTTCGCGGCCAGGCCCTCGCCTGCGCTCGCGCGCACCCACGAGAACAGCGCGTCGGACTCGACGAGCCCGCGCTCGAAGACGAGGTTGGGCCACTCGAGGACGCCGGGGAACGTGTGGACGAAGTCGTTCTGGCCGCCCTCGACGTACCGGTGCGTGCCGAGCCGCACGGAGAGCCCCGAGAGCTTGCGGAACGTGCCGATGGGCACGCCGTCGACTTCGAAGAGGAACCAGCCGGCGGTCGACGCGTCGCCGCCGAGCGCGCGCTGCTCAGAGCTGCTCACGTGCGGCCTCCCAGGCGCGGTCGTTGAGTGCCGAGACGGCACGGATGAGACGGACCCGGTCCAGGTGCTCGAGGTCGAGCACCTGGTCCAGGGGCCAGTGCAGGTGGTAGGAGAGGTAGGCGATCTCCTGCCACAGGGCGTCGGTCGGGTAGCGGAGCATCAGGCCCCGTCCCGGATCTCCTCGATCGAGGCCCGGGTGCGCGCCGAGGCGAGCGCAGGGACGGGCGCGGGCGCCTCGTCCTCGGTCTCGTCCTCGACGGCCTCGGGGACGGCGGCCGCCGCCGTGACGGCACCCGAGGGTGCCGTCACGGGGGCGGGAGCCTCGGCCTGCGCCGCGACGAGGGCCTCGTACTCGGCCTGCGAGCCGAAGTTGATGACCCCGTAGAAGTCCTGGAGGAACGCCAGGTCCGCGGCGAACAGGTTCTCGATCTCGTGGCTCGTCACCATCTCGAGCGCCCCGAGGCGCTCGACGACACGGGCGAGGATGACCACCGTGAGACGGGGGTCGTCCGGCCCGTCGACCGTCGGGTCGCGGAGCGGCTCGAGCTCGTCGCGCGCTGTCGCGAGGCGCATGACGCCCTCGCGGTGCACGTCGCCGTGACGGTCGACGTACCCGCGGGGGAGGGTGAACGCGTAGCGGGTCTGCAGGCTCACTTGACCCGCTCGAGGCGCTCGATGACGAGGGTGATGGACTCCTTGACGACCTCGTTGGAGTCGACCGAGAGCTGGTCCGTCGAGATCTTCGAGGGCCACGAGTTGAAGAAGTTGAAGCGCGCGACCTCGTTGCGGGCCGAGTCGTAGAGCACGATCGAGCCGTTCTTGCGCAGGCCCGTGCGGTCGGTGGCCTTGAGGCCCGCGCCACGGATCTCGTTGAACCACTTCCACATCTTGTCGCTCGGGGAGTCGAGCGGGGCGACGCGCGTGAGCGCGAGGTCGGCCGTCTGGACGCGGCCGCCGAGGCCCTTGACCTGCTCGGCGGCACCGCCTGCGCCGGACTGGGTGACGCTCGCGACGGCGACCTCGATGTCGAGGCCCGAGACGGAGATGAGGGCGGTGATGACCTCGCCGTCGATCTCGAGGAAGAAGTTCTGGGCGATGATCGGGTCGTTGTTGAACAGTCCGTCAACCACGGTGGTCTCCTTGGGTCAGGTCCGCGCTCAGGCGGCCGAGTTCTTGTTCTGGCTGATGCGGAAGACGACGAACTCGGCGGGCTTCACCGGGGCGATGCCGACCTCGACGACGAGCTTGCCCGCGTCGATCGACTCGGGGGTGTTCGTCGTCTCGTCGCACTTGACGAAGTACGCCTGCTGGGGCGAGGAGCCGAAGAGGGCGCCCGCCTTCCACAGTCCGTGGAGGTAGCCCGAGAGAGTGCGGTTGACGCCCTCCCAGAGCTTGACGTCGTTGGGCTCGAAGACGGCCCACTGGGTGCCCTCGAGGATCGTCGACTCGATCATGTTGAAGAGGCGACGGACGTTGACGTACTGCCAGTCGGTGTCCGAGGCGAGCGTGCGGGCGCCCCACACGCGGATGCCGCGCGTGCCGAACGGGCGGATCGCGTTGATGCCGATGGGGTTGAGGAAGCCCTGCTCGGTCTGCGTGATGGCACGCTCGACGTCGAGGACGCCGCGGAGCGTGTCGTTGGCCGGGGCCTTCCACACGCCGCGCGTGTCGTCGGTGCGGGCCCAGAGGCCTGCGACGTGGCCCGAGGCCGGGATCGACACGGTCGTCGCGCCGGCACCGCCCGTGGGGTTCTCGACCGTGATCCACGGGTAGTACATGGCGGCGAACGCCGAGTCGTACTGGGCGACCTCGGAGCGCCACTCCTTGACCTGCTGCGGCGTGAGGCCGGGCGGCGGGTCGAGGAGAGCCATGCGGTTGGGGTGGTTCTCGCAGTGTGCGACGAGGGACGTCTGCACTGCCTTCCACAGGTCGAGGTCGACGGTGCCGTCGGCGCGGGACGCGGCGGTGACGAGGTCGGGGACGACGACGATGGTCACGTCCTCGGCGATCGAGAGTCCGTTGATGCCCGAGCGGGCCGTCTCGGAGCCGGCGAAGCGGCGGCCGGTGACGGCCACGGGGATCGGGTCGGCCTTCGCGAGCGTGTACGCGCCGGGGCGCAGGACCTCGAGCTGGGCGGAGAGGTCGGTGTCCTCCTCGAGGAGGATCTCGATCTTCACCTTCGTCGACGTCGCGTTGACGACCGTCGCGGCGTCGCGCGGGCCGCCGAGCGTGAGGTCGCCGAACGACTCGACCTCGACGCCGTTCTCGACGATGCGCAGGGTGAAGGGCGCGGGACCCTCGAGGTCCTCGGGCGCCTCGTCGGTCGTCACGGTGACGGTGAGGTCGGCGTCGGGCTCGACCGAGGTCACGGCGACGGGCAGGCCGAGCGAGCGGTCCGTGGCGGGCAGCGCGAGACGCGAGGACTCGCCGGCGGGCTCGACGTGCGGGACGCGCACGATGTACGCCGCGGTGCCCCCGTTGAGGAAGAAGCCGTGGACGGACAGGGGCAGGACTGCGCCCTCGACGAAGCCTCCGTAGAGGTTCTCGAACTGCGTCCAGCTCGTCACGAGGCGCGGAGCGAGGCCCTGGGGGTCGCTCGGGTCGTCGTGCGGGGCGCGGGCGGTGAAACCGACGAAGGCGGCGACGGCGGTGGGGGCCGAGGCGAGCACCTTCTGGCTCGAGGGGACTTCCTCGACGTAAACGCCGGGTGCGGTGTAGGTGGGCACGGTTCTTCCTCTGCGTCGACGACGGTGGCCGGCAGGGCGCACCGGGCTGGTGGACGACAGCGAACGTAGGCCGCAGCGGTTGCGGACAACATCGGTAGTTGCTACGGAACTTTCACCCGGGCGGTGTAGTGTCCCGGTAGTTCATGGCTCGCGCGCGGGTCTTAGGGCCCGTGTCCGCGCTCGTGGGGGTATGTCCGGGCCGTCGGGGTGAGGTCGGGAGACGACGATGGAGGGTTCGCGCGGCCGCATGGCCGTCGACCGGCACGACAGGCACGCGGCGGCGCTGCGCCGCGCCGTGGTCCCCGCGCGCCACGGCGGCTCGCACAGCTCGACGGTCTCTCGCTCCGCGGAGGTCGAGACCGTCGCGCGCGCGATCGGCTCGGGCCGATGCGCCCTCGTCTTCGGCGAGGTGGGCGTCGGCAAGACGTACGTCGTCGACGCCGCGCAGCGGCTGCTCTCGGAGAGCGAGCCGGACCTCGAGTGGCTCATGGTGTCTGCGGACCCTGACGACGGATCCGCGCTCGCGGCGCTCTCCGTCGTCCTGCCGGAGCTCCTCGCGGCTCCCGCCGACATGGAGGACCCGATGCGCACCGCGATGGCGTACGCGGTGCTGCGCGCTCGTGCGCAGGGACGTCGCCTCGTCGTGCGGGTCGAGGACGCGCACCACCTCGACGCGATGTCGCGCCACGTGCTGGTCGGGCTCGCGCGGACGGGCGAGATCGGCCTCGTCGCGACGCTGCGCCCGGGGGTCGCGCGCCGCGCGCCGTGGGTGCAGCTGTGGAAGGACGGCGTCGCGGAGCGCATCGACGTCGCGCGCTTCACGCCTGCGGAGACGGAGCGGTACGTCGCCGAGACGCTCGGTGGCGACGTCGCGGCGGACGTCGCGATCGTGCTGTGGAACAGGACGGGTGGCAACCCGCTGTTCGTGCGCGAGCTCACCCGCGTCGCGGTCGAGTCGCGCGCCCTGCTCGCGGTGGGCTCGACGTGGGTGTGGGACCGGTGGGCGCTGCTCGACCCGCGCGTGCTCGATCTCGTCCAGCACGAGCTCGTCGGGCTGTCGGCGGCCGAGCGTCTGCTGCTCGAGCAGGTCGTCGCGCTCGGCGGCGCGCTGCCGTCGGTCGTCGACGCGCTCGACGTGTCCGGGGCGTACGTCGCGCTCGTCGCGGACCGGCTGCTCGAGGTCGTCCCGGTGCGCTCGGACGGTCCGGTGACGGTTCCTGCCTGTGTGAGAGCGCACCCGCTCGTCGCGGAGGCCCTGCGCGGGTCTGTCCCCGCGCGTGTGCGGCGTGAGGCCGTCGCGCGCTGGGAGGAGCTCACGGGTGGTGTCGCGGCGTCGGACGAGGCGCTCGTGCGGATGGTGACGGACGCGCTCGAGGTCGGGGACGCGCAGCCGATGCCACGCATCCTCGAGGCCACGACGGCCGCGCTCCGTGAGCACCGGTGCGAGCTCGTCGTGCGGCTCGTCGGCCTCGCGCTGCCGGGCGCCCGCGGCGCGGACGTGGTGCGTCTGCTCGCGACGCGCGCGTCTGCCCATCGTTTCCTGTCGCGGCCCGACGCGGCGCGTCGTGACCTCGTCACGGCGCGCGACCTCGTGGCGAGGCTCGATCTCACGGTCGCCGAGGGGCCTGAGCTCTTCAGCCTGCTCGGCCATCTCGAAGCGGAGGTGCGGCAGTTCGCGGAGGACGACGCCGACGGCGCGCTCGAGGTCCTTGCGCTGCTGCGCGACGAGGTCGGCGTGCGCTGGCCGGACGCGCCTGCGACGTGGTGGCAGGACGAGGAGATCTGCAGGCTCACGTGCCTCGCGGCGGCAGGACGGCACGCAGAGCCCATGGCGGCCGCGGAGGAGCTCTTCGCGGCGACGGCCCGGCGCCCGCACGCGGTGCTCCCGCTCGTGCCCTCGCTCGTCGCGGGCGCCGCGCAGATGCCCGGCGGGCACGGGGCGCTCGGTCTCGTCGAACGCTTCATGGGTGTGGCGACGGCGCACGCGGACTCTGCGTCCTGGGCGGTGTCGAACCTTGCGACCGCGGGCTTCGTCGCGTCGGGCCTGCTCGGCTACGTCATGTCGGCCGGCGACGTCGAGAAGCTGCTCGGTGCGACGGACCTGCCGTTCAACGTCGACGTCGTCGCGCTCAACCTGCTCCACGGGATCACAGCCATGCAGGCGGGCGACTGGCCGGTCGCGAGGGCGAGGCTCGCCGCGGCGTCGCGCCGCTACGAGCACGGCGACGTCCAGGGACGGCTCGCGGTGACGTACGCGCTCGGCGCGATCGCTGCGGCGGCCTCGGGCGAGGTCGTCGAGGCGCGCGAGCTGCTCGAGCGTGCCAGGACCGTGTCGTGGTCGGGCGTGCGGACGCTCGGCGGGTACATGGGGCTGCTGCGGCTCGACGCGCTCGCGTGGCTGCGGGACCGGGCGCTCGTCCCGGAGGCGCTCGCGCTCGCGGAGACGTGCCGGGGGGCGGGGCTCGTCCGCGTCGAGTTCGAGGCTCTGCACCGGGCCGTCGTCACGGCGCACCCTGCGGGCGGGACGCTCCTGCCGGGCGAGGAGGTCGAGGCGCTCGGGGAACGTGCGCTCGCGATCGCGCCTTTGCTTGACGGGCCGCGTGCCGCGGCGGTCGCGGCGCACCTCGAGGCTGTGCTCGCGGGTGACGACGCGCTCGCGCTGTCGGCCGTGCGTGACATGGCGGCGGCGGGGCTCTTCGTGCCGACGGCGGCGCCGGCGGTGCAGCTGACGCGGCGGGAGTCGCAGATCGCGGCGCTCGCGGCGGCGGGGCTGAGCTCGAAGGAGATCGCGGAGCGCCTCACGTTGTCGGTACGGACGGTGGACTCGCACCTGTCGCGCATCTTCGCGAAGGCGGGGGTGCGTTCCCGCCGAGAGCTGGCAGCAGCCCTCCACCTCGACCCGACCCCCTGACCCGGTCCCGTCCCACCCCCTGATCCCACGCCCCGTCCCGCATCGTCCCCTCCTGCCTCGTCCCGGTCGCGTCCCCCCGCCTCGTCCCCTCCTGCCTCGTCCCCGTCCCGTCCCCTCCTGCCTCGTACCCGTCCCACTTCGTCCCGCCCCGCAGTGTTCCGATAGCCGATCCGACCACCTCACAGGTCCCGATCCTTTGTTGAGCGCAGCGTGCGCGGGGAGCGTTCCCGTCGATAGTGGATCCGTACATCTCACATGCATGGATTGGCTATCGAGCGCAGCCTGCGCGGGGAGTGCCCTCGTCGATAGCGGATCGGTACATCTCACGTGCACGGATCGGCTATCGAGCATCGGGCGGGGGCCGCCAGCGGGTCGGTCCGCCTAGCTCCGTCCGGGGCATCGAGCGTCGCGTGCGCGGGGGAGCGTTCCCGTCGATAGCGGATCGGTACATCGCACGTGCATGGATCGGCTATCGGGACACCGCCGGGGTGAGGTTCGGTGATCAGCAGCTCGACCTCTCGACCAAATGGTCGGTTTTGGCAGTTCTGTGGTTGGAACGAGCCGACCCGTGGTGAGACAGGTTGGCGCCGGCACGCCGTCGGGGGAGGGGGCGACCGTCCGGAGAGAGACCGACGCTAGTCGTCGTCCGGGTGGGGGACGTCGCGGCCGCGGAGGGCGTCGAGCGCGCGGCGCTCGCGCTTCGTCGGGCGGCCCGAGCCGCGCTCGCGGAGCGCGACGGGCGCTGCGGCCGCGAGGCGCGGCGGCGGGGGAGGCGTGCGGTCCTCGTAGGCCTCGGCCGCGAGCGGGGCCCCGACGCGCTTGGTGAGGAGCTCGCGGACGACGACGACGCGCTCGCCAGCGTCGGTCCGGGCCCTGATCTCGTCGCCGACGCGGACCGTCGTCGACGGCTTGGCGCGCTCCCCGGCGACGCGGACGTGCCCGGCGCGGCATGCGGCGGCTGCGGCGGAGCGTGTCCGGTAGATGCGCGCGGACCACGCCCAGACGTCGACCCGGACCCTCCCACCCTCGACCATCCCCGCAGCCTATCGACCTGTCCGCCGAACCGGGCCGGAGAGCATCTCGCGAGATAGGGGCTCCGCGTCGAGATAGGGGTCGGTAGCCCACTATCTCGCGTGCGGGCCCCTATCTCGCGGACGGGCCCGGGGGATGTCGGAGGGGCGTCGTAGACTCGGGCTCATGAGCGAGCCGATGTTCCCGACCCACCCGGACGATCCCTCGGATCCCCGCGGTCCCGGCGGCTCGGCGACGAGCGTCCTCGAGCGCACGGAGCAGGCCCAGGAGGCCGAGCCCGGCGACCACGAGCGCTTCGCGCACTACGTGCGCAAGGAGAAGATCATGCAGTCGGCCATGACGGGCCGTCCCGTCATCGCGCTGTGCGGCAAGGTCTGGGTCCCGGGTCGGGACCCGCAGAAGTTCCCCGTCTGCCCCGTCTGCAAGGAGATCTACGACGGCCTGCGTGACCCGCAGGACGGCGACTCCGACGGCGGCCAGGGCGACGGCGGCCGGTGACGCCGGCCGCAGAGCAGCCTGACCTCTTCACCTCCGCGCTCACCGAACGGGTCGAGCGTGCCGCGGCGCGGGCGCGTGCCCGCATGCAGGTCGGTGGAGCCGCTCCTCGTCAGGCCGTGCAGTCCATGCCGGTGCACGCGTCGGCGGTCGCGGCGGAGCAGCTTGCTCCGGCGTTCCCGCAGCGTGCCCCGTGGGGTACGGCGACGAAGCTCCGTGCGTGGCAGGCGGAGGCGCTCGACCGCTATCGGGCGACGCAGCCGAGGGACTTCCTCGCGGTCGCGACGCCGGGCGCGGGCAAGACGACGTTCGCGCTGCGTCTGGCGACGGAGCTGCTCGAGGCCGGCACGGTGCGTCGCATCGCGATCGTCGCGCCGACCGAGCACCTCAAGCACCAGTGGGCGGACGCGGCGGCGCGCGTCGGCGTGAAGATCGACCCGAACTTCCGCAACGCACAGGGTCGCGCGGGCTCGCAGTACGACGGCGTCGCGCTCACGTATGCGCAGGTTGCTGCGAACCCTGCGCTGCACCGGGCGCGCACGGAGTCGGCGCGCACGCTCGTCATCCTCGACGAGGTGCACCACGGCGGCGACGCACTGAGCTGGGGCGACGCGCTGCGTGAGGCGTTCGAGGATGCGACGCGACGCCTGCTGCTCACGGGCACGCCGTTCCGCTCGGACACGTCGCCGATCCCGTTCGTGCGGTACGAGCGTGACCGCGACGGCATCCGGCGCTCGTCGGCGGACTACACCTACGGCTACGGCGAGGCGCTGCGCGACCATGTCGTGCGGCCCGTGATCTTCATGTCGTACTCGGGCCAGGTCCGCTGGCGCACGAAGGCGGGCGACGAGGTCGCGGCGCGCCTCGGCGAGCCCATGACCAAGGACATGGTCTCGCAGGCGTGGCGGACGGCCCTCGACCCGAACGGCGAGTGGATCCAGTCGGTCATCGCTGCGGCGGACACGCGCCTCACCGAGGTGCGCCGCACGGTCCCGGACGCGGGGGCGATGGTCATCGCGACGGACCAGACGGACGCGCGCGCCTACGCGGGTCACATCGCGCGGATCACGGGTCACTCGCCGACGGTCGTCCTCTCGGACGACGACGGCGCGGGCAAGAACATCGAGGAGTTCGCGAAGGGCGACTCGCGGTGGCTCGTCGCGGTGCGCATGGTCTCGGAGGGCGTCGACGTCCCGCGGCTCGCGGTGGGTGTGTACGCGACGAGCGCGTCGACCCCGCTGTTCTTCGCGCAGGCGATCGGCCGATTCGTGCGTGCGCGGCGCCGGGGCGAGACGGCGTCGGTGTTCCTGCCGTCGGTGCCGCAGCTGCTCGAGCTCGCGCACGCGATGGAGGCGGAGCGCGACCATGCGCTGGACCGCCCGCGCAACGAGGCGGAGGGGCAGGACCCTGAGGCCGACCTGCTCGCTGCGGCGAACCGTGAGGAGAAGGGCTCGGACGACCTGCTCGGCTCGTTCGAGGCGCTCGAGGCTCAGGCGTCGTTCGACAAGGTGCTCTTCGACGGCGGCGAGTTCGGCCTGGGCGCGGACGTCGGCTCGGACGAGGAGCTCGACTTCCTGGGCCTGCCGGGGCTCCTCGACGCGGAGCAGGTGACGACGCTCCTGCGGCAGCGCCAGGCGGGCCAGGTGGCGCGCGGGCGCCAGGAGATCGACACGGAGGAGTTCGACCACCGGCGGGCGGCAGACCTCCGCAAGGAGCTGAGCCAGCTCGTTGCGGGCTGGGCACGGCGCTCGGGCAAGCCGCACGGCACGATCCACACGGAGCTGCGCCGACGCTGCGGCGGGCCGGACGTGCCGCAGGCGACGGTCGAGCAGCTCGAGCAGCGTGTCGCGATGGTGCGCGGCTGGTTCGTCGGGCGGAAGTGAGGCGCACCGGGCGACCTGCTCGGATGTCGGGGCCCCGACGTAGGCTGGAGCCGTGATCCTCGACCTGCCTCCGGTGCGTGTCTCGACGGACCCCGGTGCCGAGATCGAGGGCGCGGGGGCCACGGACGTGCTCGCGCGCACGGAGGACGCGTGGGTGACGCTCGTGTGGAACGACCCGGTCAACCTCATGACGTACGTCGCGTACGTCTTCGAGTCGTACTTCGGCTATCCGCCGGCCAAGGCGGAGGAGCTCATGCTGCGCGTGCACCACGAGGGGCGCACGGTCGTCTCGAGCGGGGGCCGCGAGCACATGGAGCGTGACGTGCAGGCGATGCACGAGTTCGGGCTGTGGGCCACCATGCAGAAGGCGGGGGAGTCGTGA

Protein sequences of DBSCAN-SWA_3

>NZ_CP049862|1084296:1102554|1094282_1095851_-|WP_166413427.1|tail|DBSCAN-SWA
MPTYTAPGVYVEEVPSSQKVLASAPTAVAAFVGFTARAPHDDPSDPQGLAPRLVTSWTQFENLYGGFVEGAVLPLSVHGFFLNGGTAAYIVRVPHVEPAGESSRLALPATDRSLGLPVAVTSVEPDADLTVTVTTDEAPEDLEGPAPFTLRIVENGVEVESFGDLTLGGPRDAATVVNATSTKVKIEILLEEDTDLSAQLEVLRPGAYTLAKADPIPVAVTGRRFAGSETARSGINGLSIAEDVTIVVVPDLVTAASRADGTVDLDLWKAVQTSLVAHCENHPNRMALLDPPPGLTPQQVKEWRSEVAQYDSAFAAMYYPWITVENPTGGAGATTVSIPASGHVAGLWARTDDTRGVWKAPANDTLRGVLDVERAITQTEQGFLNPIGINAIRPFGTRGIRVWGARTLASDTDWQYVNVRRLFNMIESTILEGTQWAVFEPNDVKLWEGVNRTLSGYLHGLWKAGALFGSSPQQAYFVKCDETTNTPESIDAGKLVVEVGIAPVKPAEFVVFRISQNKNSAA
>NZ_CP049862|1084296:1102554|1100417_1102172_+|WP_166415205.1|DBSCAN-SWA
MPVHASAVAAEQLAPAFPQRAPWGTATKLRAWQAEALDRYRATQPRDFLAVATPGAGKTTFALRLATELLEAGTVRRIAIVAPTEHLKHQWADAAARVGVKIDPNFRNAQGRAGSQYDGVALTYAQVAANPALHRARTESARTLVILDEVHHGGDALSWGDALREAFEDATRRLLLTGTPFRSDTSPIPFVRYERDRDGIRRSSADYTYGYGEALRDHVVRPVIFMSYSGQVRWRTKAGDEVAARLGEPMTKDMVSQAWRTALDPNGEWIQSVIAAADTRLTEVRRTVPDAGAMVIATDQTDARAYAGHIARITGHSPTVVLSDDDGAGKNIEEFAKGDSRWLVAVRMVSEGVDVPRLAVGVYATSASTPLFFAQAIGRFVRARRRGETASVFLPSVPQLLELAHAMEAERDHALDRPRNEAEGQDPEADLLAAANREEKGSDDLLGSFEALEAQASFDKVLFDGGEFGLGADVGSDEELDFLGLPGLLDAEQVTTLLRQRQAGQVARGRQEIDTEEFDHRRAADLRKELSQLVAGWARRSGKPHGTIHTELRRRCGGPDVPQATVEQLEQRVAMVRGWFVGRK
>NZ_CP049862|1084296:1102554|1096077_1098762_+|WP_166413428.1|DBSCAN-SWA
MEGSRGRMAVDRHDRHAAALRRAVVPARHGGSHSSTVSRSAEVETVARAIGSGRCALVFGEVGVGKTYVVDAAQRLLSESEPDLEWLMVSADPDDGSALAALSVVLPELLAAPADMEDPMRTAMAYAVLRARAQGRRLVVRVEDAHHLDAMSRHVLVGLARTGEIGLVATLRPGVARRAPWVQLWKDGVAERIDVARFTPAETERYVAETLGGDVAADVAIVLWNRTGGNPLFVRELTRVAVESRALLAVGSTWVWDRWALLDPRVLDLVQHELVGLSAAERLLLEQVVALGGALPSVVDALDVSGAYVALVADRLLEVVPVRSDGPVTVPACVRAHPLVAEALRGSVPARVRREAVARWEELTGGVAASDEALVRMVTDALEVGDAQPMPRILEATTAALREHRCELVVRLVGLALPGARGADVVRLLATRASAHRFLSRPDAARRDLVTARDLVARLDLTVAEGPELFSLLGHLEAEVRQFAEDDADGALEVLALLRDEVGVRWPDAPATWWQDEEICRLTCLAAAGRHAEPMAAAEELFAATARRPHAVLPLVPSLVAGAAQMPGGHGALGLVERFMGVATAHADSASWAVSNLATAGFVASGLLGYVMSAGDVEKLLGATDLPFNVDVVALNLLHGITAMQAGDWPVARARLAAASRRYEHGDVQGRLAVTYALGAIAAAASGEVVEARELLERARTVSWSGVRTLGGYMGLLRLDALAWLRDRALVPEALALAETCRGAGLVRVEFEALHRAVVTAHPAGGTLLPGEEVEALGERALAIAPLLDGPRAAAVAAHLEAVLAGDDALALSAVRDMAAAGLFVPTAAPAVQLTRRESQIAALAAAGLSSKEIAERLTLSVRTVDSHLSRIFAKAGVRSRRELAAALHLDPTP
>NZ_CP049862|1084296:1102554|1093284_1093779_-|WP_166413425.1|DBSCAN-SWA
MSLQTRYAFTLPRGYVDRHGDVHREGVMRLATARDELEPLRDPTVDGPDDPRLTVVILARVVERLGALEMVTSHEIENLFAADLAFLQDFYGVINFGSQAEYEALVAAQAEAPAPVTAPSGAVTAAAAVPEAVEDETEDEAPAPVPALASARTRASIEEIRDGA
>NZ_CP049862|1084296:1102554|1087299_1089072_-|WP_166413420.1|DBSCAN-SWA
MTSAAAGVSLVPRITLDGGPLPTSLTGTLVALRVVRPLRTTAWARLELAVDDSAHVLDPTRGIGAVKVGQKVTVGGRPSDRPVVATVFEGTVTRIESVRGERGGTRLVVTAQDATALLASETAQTFVDEGLASILGKIVQSAGLRVDATGLPPAKVHYMLQAGSALRFVDDVAQRTGSDWMLDGTTLRLWPASTPRPGAEHVTLRADEVATCEVSQESGGPTRAVVTSWDPEAGAAVTGEHERKAVDGIAVSERVVLDSTSFPLDADEATRIARARLAGSGPVAARALVRRLVPLAPGSRLTLQHTWWPDDAEYVREVTTTWDRAGWSTEVVTGSRARTTLADLGGRAGDRGAAAYTHDGVVVGIVTALGAQNDARGAGRVKVEFPFLGRTITSDWARVASAGGGEGRGLLVVPEVGDEVLVAFEGSDVRRPVVVTGLHSERRKAPGTYPVEGSTVSRRAFTSRRGNLLELVDGDSAAKDHVLLALPGGETRLRLGGDAVDLTVPKGRPVKIQAGATRIVVGDDGSVTVEGTEITVRAQQRLALEAAEISVRAKGKLALEGADVSVKGQAKAALEAGGVTQVKGGMVQIN
>NZ_CP049862|1084296:1102554|1089068_1089728_-|WP_166413421.1|DBSCAN-SWA
MAAPEKAFLELEGGERIPCLYNPAELRLTRSNSWDATPRPGRPTPRLRFGGARPGVLEVSLFFDTTATGRSVAEHTGRVVEAMDIDPTLPGSDERAGDVRPPLVTFHWGEVHSFRSVIADLALAYTYFSPTGTPLRATLDLVLQQFEPEHAFGPQNPTSGTPQPHRVHRVQSGETLDRIAARYYGDATRWRPLAAANAVTDPLRLVPGTLLAVPGIEDL
>NZ_CP049862|1084296:1102554|1099397_1099796_-|WP_166413429.1|DBSCAN-SWA
MVEGGRVRVDVWAWSARIYRTRSAAAAACRAGHVRVAGERAKPSTTVRVGDEIRARTDAGERVVVVRELLTKRVGAPLAAEAYEDRTPPPPPRLAAAAPVALRERGSGRPTKRERRALDALRGRDVPHPDDD
>NZ_CP049862|1084296:1102554|1099959_1100292_+|WP_166413430.1|DBSCAN-SWA
MSEPMFPTHPDDPSDPRGPGGSATSVLERTEQAQEAEPGDHERFAHYVRKEKIMQSAMTGRPVIALCGKVWVPGRDPQKFPVCPVCKEIYDGLRDPQDGDSDGGQGDGGR
>NZ_CP049862|1084296:1102554|1092651_1093125_-|WP_166413423.1|tail|DBSCAN-SWA
MSSSEQRALGGDASTAGWFLFEVDGVPIGTFRKLSGLSVRLGTHRYVEGGQNDFVHTFPGVLEWPNLVFERGLVESDALFSWVRASAGEGLAANGGKLVRSTGAVTALDYTGERLRAWDVDGVFAVAWDGPTFDVESNATLVERLEVSHEGFRAKTS
>NZ_CP049862|1084296:1102554|1093111_1093285_-|WP_166413424.1|DBSCAN-SWA
MLRYPTDALWQEIAYLSYHLHWPLDQVLDLEHLDRVRLIRAVSALNDRAWEAAREQL
>NZ_CP049862|1084296:1102554|1102236_1102554_+|WP_166415206.1|protease|DBSCAN-SWA
MPPVRVSTDPGAEIEGAGATDVLARTEDAWVTLVWNDPVNLMTYVAYVFESYFGYPPAKAEELMLRVHHEGRTVVSSGGREHMERDVQAMHEFGLWATMQKAGES
>NZ_CP049862|1084296:1102554|1084296_1084911_-|WP_166413417.1|tail|DBSCAN-SWA
MSRRPGWLVDQLPPAMVDEDFFRRFVTIFEEQADTLQAHGDNLDVLADTRLTPAEMLPWLASWIGVRALDGGAGVTSGSDAPSDGAGDGGSPEVPGEARQRALLEAWAATLMSRGTPGALRTVLTALCGPGVVVREGGGVFAEGACPADTAWLEVELPSTGGLDPRSLLGLVLDEIPAHVRATVRVARDQIYPAVTADLLEGVR
>NZ_CP049862|1084296:1102554|1086883_1087300_-|WP_166413419.1|DBSCAN-SWA
MENASSAASFVGRGFTWPLRVDASGSIALTDGSGDLDDAIRVVLLTAPGERLMRPQFGCRIWDLLFEPVTANLLGLVDRAVRDALAQWEPRIEVLDVTPRQDDDNPGLVLIDLTYRVKATNDRRNLVHPFYVIPHEES
>NZ_CP049862|1084296:1102554|1089727_1092655_-|WP_166413422.1|DBSCAN-SWA
MSIPTLPPGPTAPDQPQGPAHLRPAGALTRFRAGRLGLTAAGSAAFARGLARTPAVRRPAPLTTALRETTEVGAPPAARSVRAPRWWSPAPDAPADDDAQRPSRTPVAAPPRGLARAASRIDRDSWTPGRLGVSATPKAVPMRLPAEVAAAGSMVTSLDSRRRSVAPSRGPAPRPTGSGPTDGAAGSRRAAGPAATQTPPGAPAPRAAGAPALPAVRRRTAPPRLARRRAAASRTAAAARATLAGSAMLPGSSAATRPTTGVAASGVAASNVAASSPTADRSSTRDSSARHTEMVPDAPAPAASVHELPTSPEVRRASAERHPGTWSASLPRAASSRSLLGHAPEASAVTRSAPALRRSTASGQRAVAGARTGALTLRPTALVRPAQADAGHVPAAHPGSRGAVADVRRATASPAPAASPHVSSAGPGTSGTTTAAPSTTHPSTTGRPTTGTDATPASAGGTSTASTSGAGPTSRGPSPTTDAATPAPTAGLTAGPQAATSHVTPSHLTMSHVPLRRALAVPGSLAAQSASARARVGAPDGRTSTGTSAARAADPTDGTAAPTLTGPARDGDHAVARVVRPVPGMLARRADVRGAGVAAAQPGKVTAVRRQVAVTRRDDAAARSAATLALTGGTTSATPGAPSSRGVVTARAAGAASSVSTTGAAPGGLDVASAVLPSSAGGATGLGSPSGVPAGSVRAPGIPLSTAAARSEAVGHATRSVSSSGSTSAARSSAVLTSPASDVRLGAGARAVRRATGPTTPLAVGGSPAHDGATRAAASTHPWRHAPAVRRTPSGPGRTAGTDPAHHSGTSLAGRATPPVAGRPAQRGPAAPATASAWRSSLTDAATVPLRRSVLPPRAPARVAAPVPGAPAVPAVARLGASHDDTAAGLSILRRALARADSALSPSSEEPTMSTLPTTGAARASAGELHLDERLLARLADALEDDLTDRVARRVERRLLEESALRTTGLTPGAF
>NZ_CP049862|1084296:1102554|1093775_1094255_-|WP_166413426.1|tail|DBSCAN-SWA
MVDGLFNNDPIIAQNFFLEIDGEVITALISVSGLDIEVAVASVTQSGAGGAAEQVKGLGGRVQTADLALTRVAPLDSPSDKMWKWFNEIRGAGLKATDRTGLRKNGSIVLYDSARNEVARFNFFNSWPSKISTDQLSVDSNEVVKESITLVIERLERVK
>NZ_CP049862|1084296:1102554|1084907_1086884_-|WP_166413418.1|plate|DBSCAN-SWA
MPPIIPPNLDDRSFQDIVDETKRLIPRHTPEWTNHNVSDPGVALVELFAWMSEMVLFRVNQVPERMYAHFLGLVGIEPFGPSAASADLTFWFSAPARAEVVVPAGVEVATSPAASGSASDDVVFTTVREAVARPASLRAVMTSAAGSDQLVDGWADLAYRGTSLAVFPSPEITLDDATYLGFTGSLADHALELTVAADVLGIGIDPTDPPLVWEAWDGEAWVRLTVHEDTTGGLNRDGRVVLLLPGSHPPLTLGGTGAHWVRVRLVRAAPGRPTYRTSPRLTSLDVGVVGVTVPAEHVTGRPGEVLGRSTGTAGQVFRVAHTPVLARRPSEEILVVTTSDAEPWTEVADFAASGPTDRHVVWDSATGEVRFGPSVRHPDGRVRQHGAIPADGAQVRVSPYRSGGGARGNVGPGTLVTPRTTLPMVASVANTTAASGGVDPETVEEAKVRGPLTLRTGRRAVTAGDYERLALAASPAVARARCLPLGDAVAGRAGAVRVLLVPAAAPRGAAEDRDIDDLALSPELRARVGAELDACRLVGVGLEVGAPFYQGASAAVLVRALPGRPAAVVRQRVLEAIHRFVDPLHGGTDGAGWPFGEDLTSAALAHVVDEVDGVERVEEVTLFDYDLRGRRRLGDSQDALTLTPGALFVSAAHRVVVR

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_166413417.1|1084296_1084911_-|tail	phage tail protein	NA	NA	NA	NA
WP_166413418.1|1084907_1086884_-|plate	putative baseplate assembly protein	NA	NA	NA	NA
WP_166413419.1|1086883_1087300_-	GPW/gp25 family protein	A0A219YDA8	Aeromonas_phage	7.0e-06	32.1
WP_166413420.1|1087299_1089072_-	hypothetical protein	NA	NA	NA	NA
WP_166413421.1|1089068_1089728_-	LysM peptidoglycan-binding domain-containing protein	NA	NA	NA	NA
WP_166413422.1|1089727_1092655_-	hypothetical protein	NA	NA	NA	NA
WP_166413423.1|1092651_1093125_-|tail	phage tail protein	NA	NA	NA	NA
WP_166413424.1|1093111_1093285_-	hypothetical protein	NA	NA	NA	NA
WP_166413425.1|1093284_1093779_-	hypothetical protein	NA	NA	NA	NA
WP_166413426.1|1093775_1094255_-|tail	phage tail protein	NA	NA	NA	NA
WP_166413427.1|1094282_1095851_-|tail	phage tail sheath family protein	J9PVC2	Bacillus_phage	2.9e-68	34.0
WP_166413428.1|1096077_1098762_+	hypothetical protein	NA	NA	NA	NA
WP_166413429.1|1099397_1099796_-	RNA-binding S4 domain-containing protein	NA	NA	NA	NA
WP_166413430.1|1099959_1100292_+	DUF3039 domain-containing protein	NA	NA	NA	NA
WP_166415205.1|1100417_1102172_+	DEAD/DEAH box helicase family protein	I4AZM6	Saccharomonospora_phage	1.1e-89	36.9
WP_166415206.1|1102236_1102554_+|protease	ATP-dependent Clp protease adapter ClpS	NA	NA	NA	NA