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_CP024593	Porphyromonas gingivalis strain KCOM 2804 chromosome, complete genome	9 crisprs	cas13b,cas3,DEDDh,cas2,cas1,cmr6gr7,cmr5gr11,cmr4gr7,cmr3gr5,cas10,cmr1gr7,cas4,cas7b,cas8b4,cas5,cas6,RT,PD-DExK	1	20	0	3

1. NZ_CP024593

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP024593_1

• CRISPR_ID: NZ_CP024593_1
• CRISPR_location: 30013-30132
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP024593_1

Consensus_repeat	Method
CTTAAAACCCTCCACCCTTTATACTATAACCC	CRISPRCasFinder

spacers of NZ_CP024593_1

>1.1|30045|56|NZ_CP024593|CRISPRCasFinder
CTCCACCCTTTATACTATAACCCGGCAAGCGGGGATTTTGTTTTTGCCCCGCCGCT

CRISPR arrays and Neighbor proteins around NZ_CP024593_1

CRISPR arrays

The CRISPR arrays of NZ_CP024593_1

>merge|NZ_CP024593|1|30013-30132|CRISPRCasFinder
CTATAAACCCTTCTGACTTTATACTTAAAACCCTCCACCCTTTATACTATAACCCGGCAAGCGGGGATTTTGTTTTTGCCCCGCCGCTCTTAAAACCCTCCACCCTTTATACTATAACCC

>NZ_CP024593|1|1|30013-30132|CRISPRCasFinder
CTATAAACCCTTCTGACTTTATACTTAAAACC	CTCCACCCTTTATACTATAACCCGGCAAGCGGGGATTTTGTTTTTGCCCCGCCGCT
CTTAAAACCCTCCACCCTTTATACTATAACCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024593.1|WP_053444653.1|28621_29128_-|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|274357
NZ_CP024593.1|WP_013815741.1|20926_22888_+|threonine--tRNA-ligase	unknown	unknown	gnl|CDD|234752
NZ_CP024593.1|WP_099811435.1|34113_35055_-|phosphoribosylaminoimidazolesuccinocarboxamide-synthase	unknown	unknown	gnl|CDD|183621
NZ_CP024593.1|WP_021661987.1|32598_33348_-|shikimate-dehydrogenase	unknown	unknown	gnl|CDD|223247
NZ_CP024593.1|WP_099896679.1|41224_42184_-|HpaII-family-restriction-endonuclease	unknown	unknown	gnl|CDD|370560
NZ_CP024593.1|WP_099811441.1|39516_40734_+|S-adenosylmethionine:tRNA-ribosyltransferase-isomerase	unknown	unknown	gnl|CDD|234666
NZ_CP024593.1|WP_005875412.1|35104_36097_-|PhoH-family-protein	unknown	unknown	gnl|CDD|376820
NZ_CP024593.1|WP_099811445.1|42264_43023_-|HNH-endonuclease	unknown	unknown	gnl|CDD|379157
NZ_CP024593.1|WP_099811439.1|37062_39378_-|alpha-mannosidase	unknown	unknown	gnl|CDD|273488
NZ_CP024593.1|WP_004584226.1|23675_23873_+|50S-ribosomal-protein-L35	unknown	unknown	gnl|CDD|234676
NZ_CP024593.1|WP_021663949.1|19337_19556_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_005875419.1|28071_28632_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_099810581.1|17811_18756_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_052073437.1|43019_43229_-|hypothetical-protein	unknown	unknown	gnl|CDD|281799
NZ_CP024593.1|WP_099811431.1|22992_23598_+|translation-initiation-factor-IF-3	unknown	unknown	gnl|CDD|234582
NZ_CP024593.1|WP_005875425.1|27279_28056_-|DUF4252-domain-containing-protein	unknown	unknown	gnl|CDD|379445
NZ_CP024593.1|WP_099810657.1|24818_25721_+|IS982-like-element-IS195-family-transposase	unknown	unknown	gnl|CDD|372648
NZ_CP024593.1|WP_012457918.1|23985_24333_+|50S-ribosomal-protein-L20	unknown	unknown	gnl|CDD|179959
NZ_CP024593.1|WP_005875423.1|33344_34082_-|bifunctional-demethylmenaquinone-methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol-methylase-UbiE	unknown	unknown	gnl|CDD|273884
NZ_CP024593.1|WP_099811433.1|30246_32571_-|BamA/TamA-family-outer-membrane-protein	unknown	unknown	gnl|CDD|366466

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP024593.1|WP_053444653.1|28621_29128_-|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	5.28763e-32
NZ_CP024593.1|WP_013815741.1|20926_22888_+|threonine--tRNA-ligase	gnl|CDD|234752	PRK00413, thrS, threonyl-tRNA synthetase; Reviewed.	0
NZ_CP024593.1|WP_099811435.1|34113_35055_-|phosphoribosylaminoimidazolesuccinocarboxamide-synthase	gnl|CDD|183621	PRK12607, PRK12607, phosphoribosylaminoimidazole-succinocarboxamide synthase; Provisional.	0
NZ_CP024593.1|WP_099896679.1|41224_42184_-|HpaII-family-restriction-endonuclease	gnl|CDD|370560	pfam09561, RE_HpaII, HpaII restriction endonuclease. This family includes the HpaII (recognizes and cleaves C^CGG) restriction endonuclease.	5.62611e-120
NZ_CP024593.1|WP_099811441.1|39516_40734_+|S-adenosylmethionine:tRNA-ribosyltransferase-isomerase	gnl|CDD|234666	PRK00147, queA, S-adenosylmethionine:tRNA ribosyltransferase-isomerase; Provisional.	6.10319e-132
NZ_CP024593.1|WP_005875412.1|35104_36097_-|PhoH-family-protein	gnl|CDD|376820	pfam02562, PhoH, PhoH-like protein. PhoH is a cytoplasmic protein and predicted ATPase that is induced by phosphate starvation.	1.76244e-122
NZ_CP024593.1|WP_099811445.1|42264_43023_-|HNH-endonuclease	gnl|CDD|379157	pfam13391, HNH_2, HNH endonuclease.	1.40419e-14
NZ_CP024593.1|WP_099811439.1|37062_39378_-|alpha-mannosidase	gnl|CDD|273488	TIGR01180, immunoreactive_89kD_antigen_PG87, alpha-1,2-mannosidase, putative. The identification of members of this family as putative alpha-1,2-mannosidases is based on an unpublished characterization of the aman2 gene in Bacillus sp. M-90 by Maruyama,Y., Nakajima,M. and Nakajima,T. (Genbank accession BAA76709, pid g4587313). Most members of this family appear to have signal sequences. Members from the dental pathogen Porphyromonas gingivalis have been described as immunoreactive with periodontitis patient serum. [Cell envelope, Biosynthesis and degradation of surface polysaccharides and lipopolysaccharides].	0
NZ_CP024593.1|WP_004584226.1|23675_23873_+|50S-ribosomal-protein-L35	gnl|CDD|234676	PRK00172, rpmI, 50S ribosomal protein L35; Reviewed.	1.91794e-21
NZ_CP024593.1|WP_099811431.1|22992_23598_+|translation-initiation-factor-IF-3	gnl|CDD|234582	PRK00028, infC, translation initiation factor IF-3; Reviewed.	9.66533e-86
NZ_CP024593.1|WP_099811433.1|30246_32571_-|BamA/TamA-family-outer-membrane-protein	gnl|CDD|366466	pfam01103, Bac_surface_Ag, Surface antigen. This entry includes the following surface antigens; D15 antigen from H.influenzae, OMA87 from P.multocida, OMP85 from N.meningitidis and N.gonorrhoeae. The family also includes a number of eukaryotic proteins that are members of the UPF0140 family. There also appears to be a relationship to pfam03865 (personal obs: C Yeats). In eukaryotes, it appears that these proteins are not surface antigens; S. cerevisiae YNL026W (SAM50) is an essential component of the Sorting and Assembly Machinery (SAM) of the mitochondrial outer membrane. The protein was localized to the mitochondria.	7.602e-20
NZ_CP024593.1|WP_052073437.1|43019_43229_-|hypothetical-protein	gnl|CDD|281799	pfam03852, Vsr, DNA mismatch endonuclease Vsr.	8.34671e-18
NZ_CP024593.1|WP_005875425.1|27279_28056_-|DUF4252-domain-containing-protein	gnl|CDD|379445	pfam14060, DUF4252, Domain of unknown function (DUF4252). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 154 and 182 amino acids in length.	1.63786e-21
NZ_CP024593.1|WP_099810657.1|24818_25721_+|IS982-like-element-IS195-family-transposase	gnl|CDD|372648	pfam13612, DDE_Tnp_1_3, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contains three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction.	6.50604e-102
NZ_CP024593.1|WP_012457918.1|23985_24333_+|50S-ribosomal-protein-L20	gnl|CDD|179959	PRK05185, rplT, 50S ribosomal protein L20; Provisional.	7.11443e-59
NZ_CP024593.1|WP_005875423.1|33344_34082_-|bifunctional-demethylmenaquinone-methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol-methylase-UbiE	gnl|CDD|273884	TIGR01934, methylase_mitochondrial, ubiquinone/menaquinone biosynthesis methyltransferases. This model represents a family of methyltransferases involved in the biosynthesis of menaquinone and ubiqinone. Some members such as the UbiE enzyme from E. coli are believed to act in both pathways, while others may act in only the menaquinone pathway. These methyltransferases are members of the UbiE/CoQ family of methyltransferases (pfam01209) which also contains ubiquinone methyltransferases and other methyltransferases. Members of this clade include a wide distribution of bacteria and eukaryotes, but no archaea. An outgroup for this clade is provided by the phosphatidylethanolamine methyltransferase (EC 2.1.1.17) from Rhodobacter sphaeroides. Note that a number of non-orthologous genes which are members of pfam03737 have been erroneously annotated as MenG methyltransferases. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	1.95102e-118
NZ_CP024593.1|WP_021661987.1|32598_33348_-|shikimate-dehydrogenase	gnl|CDD|223247	COG0169, AroE, Shikimate 5-dehydrogenase [Amino acid transport and metabolism].	6.1822e-78

Protein sequences

>NZ_CP024593.1|WP_053444653.1|28621_29128_-|sigma-70-family-RNA-polymerase-sigma-factor
MNTIAFKEIFLPIRPSIRAVCHAFLRDDEEAEDATQEVYLRLWEARMRLDGLDNPRAYAIRIARNYCLNLIRKASNSPYPTSLEAAEVQEVSETLGGEADLLLSEQIGRLRQWLRGVSELHRTVFAMSHFRRLSNGEIAERLGLTEGNVRVILCRLRREAKEVMKDDA
>NZ_CP024593.1|WP_005875419.1|28071_28632_-|hypothetical-protein
MMREERNKIDRLLESFYAGTTSPQEELELYCLLEGLPDAAPYHSDLQLLRALIGLPERETAMEDDSDKVLLEKMASWEDRVRHPSRRLSLRLVRYGAVACVALALAIGVAVELNTVGRLSSNRNGIALDRDEAVRETAYAMELLEYCLDRGADAEGEFVEMLGWEEEALYAETAMSEEEYERNTIE
>NZ_CP024593.1|WP_005875425.1|27279_28056_-|DUF4252-domain-containing-protein
MKAKMIVALIVAICMLSPVADAQRIKVEELRKDNGIESVYLSKPMLKMASKYLKRKTDISINTSLLDGMYIFSTDMNRSSSAALIRRTFSPIMGGSRKDYEELMSVQDGNERIGFYAEKGKKNTFRTLVLYTEDAEEIRALVMEGTFTREQLNQMIYPNGRSRYFRKEWNVLKPDNSEAMRKYRKQKEKYYQEYMKAQKKQNQEWRKEREKLRREMEKARKQYREEMKKAREELRKSGAESYLIFPDSTWKIDMADLD
>NZ_CP024593.1|WP_099810657.1|24818_25721_+|IS982-like-element-IS195-family-transposase
MKTNIVDVFCIIDDFSKLFDETIKKKTLEEADKKRRNRKFKMSDSEVMTILILFHLSRYRDLKAFYLQYITHSCRSEFPHLVSYNRFVELQSRVGFKLIAFLNMCCLGQCTGISFIDSTPLKVCHIKRAHGHRTMRGWAQKGKSTMGWFYGFKLHIVINDRGEIINYQITPGNCDDREPLKDGTFTKNLFGKLIADRGYISQNLFDRLFVDDIHMITKIKKNMKNSLMHLYDKVLLRKRALIETVNDMLKNVCQIEHTRHRSVNNFVTNLISGIIAYNILPKKPELNIEIIRNPNFPISA
>NZ_CP024593.1|WP_012457918.1|23985_24333_+|50S-ribosomal-protein-L20
MPRSVNHVASRAKRKRILKLTRGYFGARKNVWTVAKNTWEKGLTYAYRDRKNKKRNFRALWIQRINAAARLEGMSYSRLMGALHANGIEINRKVLADLAMNHPEAFRAIVAKVKN
>NZ_CP024593.1|WP_004584226.1|23675_23873_+|50S-ribosomal-protein-L35
MPKLKTNSGAKKRFALTGTGKIKRKHAFKSHILTKKTKKQKRNLTYFSTVHKVDENAVKQLLCLR
>NZ_CP024593.1|WP_099811431.1|22992_23598_+|translation-initiation-factor-IF-3
MAIDKTKNQHRINEAIRVKEVRLVGDNVEQGVYNIQEARRIAESQDLDLVEISPNADPPVCRVTDYQKFVYQLKKKAKEQKAKSVKIVIKEIRFGPQTDDHDYNFKLKHAKEFLQEGSKVKAYVFFRGRSILFKEQGEVLLLRFANDLEDFARVEQMPILEGKRMTVMLTPKSASKKGHTPPKTQVEASKQANESAETEEE
>NZ_CP024593.1|WP_013815741.1|20926_22888_+|threonine--tRNA-ligase
MIKITFPDGNFREYEAGITGWDIAGSISPRLQQDVLAAGVNGQVWDLHRPINEDAEVKLFKWDDAEGKHAFWHSSAHLMAEALEELYPGIKFGIGPAIENGFYYDVDPGEGISIKDADLPAIEKRMQDLAARKETIIRRDIAKADALRMFGDKDDQYKVELISELADGTITTYTQGGFTDLCRGPHLPNTGYIKAIKLLSVAGAYWRGDEKRKQLTRIYGISFPKKKMLDEYLELLEEAKKRDHRKIGKELELFAFSQNVGAGLPLWLPRGTQLRLRLEDFLKQIQKHFGYQQVITPHIGNKNLYITSGHYAKYGQDSFRPINTPQEGEEFMLKPMNCPHHCEIFKITPHSYRDLPIRLAEFGTVYRYEQSGELHGLTRVRGFTQDDAHLFCRPDQLKEEFCKVMDIIFIIFKALDFKNFEAQISLRDKVNREKYIGSEENWERAERAIIEACEEKGLPAVIEYGEAAFYGPKLDFMVKDALGRRWQLGTIQVDYNLPERFDLEYTGEDNKKHRPVMIHRAPFGSMERFVAVLIEHTAGKFPLWLTPDQVVVLPVSERFNEYAHRVAKELNQRDIRVQVDDRNEKVGRKIRDNELKRIPYMLIVGENESREEEVSVRKQGDGDMGIMKITTFAELIEKEVDDMISAWRKDYQN
>NZ_CP024593.1|WP_021663949.1|19337_19556_+|hypothetical-protein
MNFRSIGGYRTPHNTAISKPDHDFTNKGYSGLRVIQNSILVRPKTRAKKVFNNEAEFGMILNKHLKERGQSE
>NZ_CP024593.1|WP_099810581.1|17811_18756_+|hypothetical-protein
MKKCPCCQSLQTKRNGIRHFRQLYKCTHCGYQFRTTNRISLDELWERYLEHKQTISELAAYYQVSASTIKRRLSEVQQVWEQPLLEQAGFVHIDATYWGRGAGILLAIDHHTARPLYLEFIRNECAQDYRRALESISRRGYIIRGVVVDGTRTLFSLSLNIPVQMCQYHMRQIISRYLTKRPKLLASRDLLLLIDSLSNQTYEGFNQAFQAWKSKWHDTIMRRSLLKSGKSRYRHRKLRSAIHSIEFYLPYLFTYQQAQCIGMPNTNNKIEGTFSALKRKINCHSGMSAANRQRLICGFFLAWKASLCNVKQEP
>NZ_CP024593.1|WP_099811433.1|30246_32571_-|BamA/TamA-family-outer-membrane-protein
MSSHSVRYLIGIAGCLLLMLASSCSVTRYVPDGSRLLDRVTIASETDSIALPEDIRDYTLQQPNYRLFGMTRWLLRVYSSSNPNSNSWWNRSLRKMGEPPVLIDSVLTERTANRLAKAMAGDGFLDATARAVVDTGLYKKARITYLIQPGSRYYIRNMALDVKNPLLPPVALGNSLPSAYKVGISEGSPLSPIVLDEERKAIARHMRNNGFWKFSAEDVYYEADTTVSGGSGTKSADLKLVVNGIGRYPYRIGRVFFHADYDPLESDFRVQELPRIDSISRGDYTVYYGSRGRYIRASALTRSVSVTPGAFFCEDDVERSYIKLNALPIVRNVNIRFVEHNGKDEIAPTDSSRLVDCYILTVPAKSKSFEAEVLGTNSAGDFGAALSLGFTDRNLFRGAEMFNIKLKGAYEAIRKGSHSFMEYGVESSLRFPRLLFPFISDETRRRLRASTEWKIGYNYQTRPEFDRVILSAQLNYSWQTYLHNRLRHTIRLLDVDYLHLPYIDPDFAQSLPPTTALYNYTEQFILGSAYILNYTTASSMERTVSNPFTARFSIQTAGNLLQAISYLTDSPKDEHGLYKMFGLHYAQFVKLDLDLAKTVLLEKDNTLALHLGFGLAFPYGNARHIPFELRYFAGGSNSVRGWSVRTLGPGSMKMTPDKTFFDQMGDIRLDLNVEYRTKLFWKFRAAAFVDAGNVWTIKEYENQEDGLFRFDRFYKEIALAYGLGLRLDFDYFLVRLDAGLKAYDPQQTGRYKWAITRPNLSSNFAWHIAVGYPF
>NZ_CP024593.1|WP_021661987.1|32598_33348_-|shikimate-dehydrogenase
MKKYGLIGYPLAHSLSAEFFNAKFKTEGINAVYELFPLESLSQLKSLLSLHPSLQGFNVTSPYKVEVMRYLDRIDEEAELTGAVNTIRVERARFRRPHLVGYNTDVKGFADSLELIRKPWHTQALVLGSGGAALAVMRALKKMGIAHRQVSRTPSAPGVYAYSDLTPEIIERHKLIVNATPVGMYPHIDQCPSIPFEGIGAEHLCYDLIYNPQETIFMHRAQAQGASVQNGLEMLLIQALCSWRIWNER
>NZ_CP024593.1|WP_005875423.1|33344_34082_-|bifunctional-demethylmenaquinone-methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol-methylase-UbiE
MQSPERITPYDTECPKNEQVEAMFNHIAGHYDRLNHLFSWGMDRVWRQKAIRMIEPFAPHTVLDVATGTGDLAIEICRHIPSVKQVTGVDLSLEMMRIGEQKVRSENLDNRITFMQKDCLDLPFADHSFDAVTVAFGLRNFQNIKLGLEEMYRVLNEGAPLMILELSRPVSFPWKQGYNFYASHVIPVVGRFLSQDAEAYTYLPESIAAMPQREELADLMLSVGFREAYYRSLSLEVATVYMGLK
>NZ_CP024593.1|WP_099811435.1|34113_35055_-|phosphoribosylaminoimidazolesuccinocarboxamide-synthase
MKETLARTDFRLPGQKAVYRGKVRDVYTLENDLLVMIATDRISAFDVVLPAGIPYKGQVLNQIAAHYLDATRDIVPNWKIATPDPMVTIGHRCEPFKVEMVIRGYITGSAWRAYAAGERVLCGLPLPEGMRENQRFEHPIITPTTKADEGHDENISRQEIIAQGLVSKEDYEQIERYTYALFERGTQMAAEKGLILVDTKYEFGKKDGKIYLIDEIHTPDSSRYFYAEGYQERFERGEAQKQLSKEFVRQWLIENGFQGKPGQQIPEMTEAYCDSVSERYIELYERVVGKPFEKADLINLAERIEKNITEYLR
>NZ_CP024593.1|WP_005875412.1|35104_36097_-|PhoH-family-protein
MLITERIYVLEDVDVQAFLGVNNSNLMLLRTLFPKLRLVAHHNVLKIMGDSRETDRFLEVLEPMVAYCREYNLLPEDVILRIAQGAKLPADDVPKHLILHGTGGKSIIARGDNQQKLVEAFEANDLVFAIGPAGTGKTFVAISLAVRALKSKQVRRIILSRPAVEAGEKLGFLPGEMKDKLDPYLQPLYDALEEMIPAVKLKEYIENNIIQIAPLAYMRGRTLNDAVVILDEAQNTTELQMKMFLTRLGANAKMIVTGDITQTDLPRGVHSGLRQALNILQGTRGIGYIAFQRADIVRHPLVQRVVDAYDRYDAERKKEAEAAAVVAQTI
>NZ_CP024593.1|WP_099811439.1|37062_39378_-|alpha-mannosidase
MLTIRNFLLYCCLSLIAFATDAQSSVSSGRRLTEYVNPFIGTANYGTTNPGAVLPNGLMSVTPFNVSGSTENRFDKDSRWWSAPYSADNSYCIGFSHVNLSGVGCPELSGILLMATSGTFDPDYCHYGSSLSREYARPGEYKAVLDKYGIDAAVTVTERTALTEFAFPEGEGHILLNLGQALSNESGACVRFLNDSTVVGSRLMGTFCYNPQAVFRQYFVLQVSRRPISAGYWKKQPPMTVEAQWDSTAGKYKLYDSYRCEMSGDDIGVRFSFNCDQGEKIYVRSAVSFVSEANALYNLEAEQEEVFKSVGGNPAKAFSVIRSRAIERWEEALGTVEVEGGTPDERTIFYTALYHLLIHPNILQDANGEYPMMGSGKTGNTAHDRYTVFSLWDTYRNVHPLLCLLYPEKQLDMVRTLIDMYRESGWLPRWELYGQETLTMEGDPSLIVINDTWQRGLRAFDTATAYEAMKKNASSAGATHPIRPDNDDYLTLGFVPLREQYDNSVSHALEYYLADWNLSRFAHALGHKEDAALFGKRSLGYRHYYNKEYGMLRPLLPDGSFLTPFDPKQGENFEPCPGFHEGSAYNYAFFVPHDIQGLARLMGGAKVFSERLQKVFDEGYYDPTNEPDMAYPYLFSYFPKEAWRTQKLTRELIDKHFCNAPNGLPGNDDAGTMSAWLVYSMLGFYPDCPGNPTYTLTSPVFPRVRIRLNPQYYPQGELVITTNTENQPTDSIYIHTVSLGNKTLPHGTRHISHADLVRCGHLRYELSNRPR
>NZ_CP024593.1|WP_099811441.1|39516_40734_+|S-adenosylmethionine:tRNA-ribosyltransferase-isomerase
MITTTDISIADYDYPLPEERIAKHALPQRDACKLLVYDKGEIKDAVFSQLSEVLPSGSMLVRNNTRVIRARLLFRKSTGATIEVFCLEPVSPAQYELSLTARGSCTWHCMVGNAKRWRSGDLQMEIPSPQGGSILLTASHDPAANGCIRFSWENDHYTFGEILEMAGILPIPPYLNRDTEEEDLETYQTVYARNLGSVAAPTAGLHFTEEEFERLRAQGTPVVDVTLHVGAGTFRPVKSETIGEHRMHRELIVIERSSLEALRDWQGSIVAVGTTSVRTLESLYWLGRSLSIAPHTPQESLKVNQWEAYENEDAALSRSETIRIILDWMDEQGVETLIFPTEILIAPGYRYRMVDAMITNFHQPRSTLLLLVSAFIGEDWKAVYHHALESGYRFLSYGDGSLLIP
>NZ_CP024593.1|WP_099896679.1|41224_42184_-|HpaII-family-restriction-endonuclease
MILRKDKDGDIKYSLQERDVVIQTPTAKELLRVAASIFLVEADKLLKAINENKGAFAVPYIETFMNGIYCHSLKAKSSDKTDIRIILHDRRTKMNSEMGFSIKSQLGSNSTLLNASKATNFNFKIKGAKFSNQDICEINSLGSKKDKVIKRVNAIKKKGATLVFDKVDNCIFRNNLIMLDGDLPMIIANLLLEQFNSGISTLKELAEKLSEVNPLNYDITQSSPFYTYKIKHLLTSAALGMMPATPWSGIYDANGGYLVVKKDGEILCYHFYDRNRFEDYLFSNAYLERSSTTRHEYASIIKEVDGSLSFKLNFQIRLK
>NZ_CP024593.1|WP_099811445.1|42264_43023_-|HNH-endonuclease
MNNWTREETIIAFNLYCKIDIRNSHKNHPLIIKYAKLLGRTPSALNMKIGNIARLDPDLKQKGILGLTHGAKSEQLVWDEFYGNPDLLAYESEKLIAIYSQKSIEESTGIEMMDLPNGKEREAIVKQRVNQSFFRSTVLNAYDYHCCISGISIPTLLEACHIIGWSEDSSIRTNPQNGLCMNPLFHKAFDNFLVTITPDMIIVISEEMITRVAKTSFQDYLRGLNGRQIMLPNKFMPRKDFLNIHYERFKKR
>NZ_CP024593.1|WP_052073437.1|43019_43229_-|hypothetical-protein
MDRLTKEQRHRNMSLNKGKGTKLEILFGKLLWNAGIRYRKNDKEIFGKPDFVIRKMYYFENFHNNIFAL

Crispr_ID: NZ_CP024593_2

• CRISPR_ID: NZ_CP024593_2
• CRISPR_location: 375657-375764
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP024593_2

Consensus_repeat	Method
AGGAATTTTTTTGCCGAAATCGCTTC	CRISPRCasFinder

spacers of NZ_CP024593_2

>2.1|375683|56|NZ_CP024593|CRISPRCasFinder
TTGCAAGCTGCAAACAGGAATTTTTTTGCCGAAATCGCTTCTTGCAAGCTGCAAAT

CRISPR arrays and Neighbor proteins around NZ_CP024593_2

CRISPR arrays

The CRISPR arrays of NZ_CP024593_2

>merge|NZ_CP024593|2|375657-375764|CRISPRCasFinder
AGGAATTTTCTTGCCGAAATTGCTTCTTGCAAGCTGCAAACAGGAATTTTTTTGCCGAAATCGCTTCTTGCAAGCTGCAAATAGGAATTTTTTCGCCAAAGTAGCTTC

>NZ_CP024593|2|2|375657-375764|CRISPRCasFinder
AGGAATTTTCTTGCCGAAATTGCTTC	TTGCAAGCTGCAAACAGGAATTTTTTTGCCGAAATCGCTTCTTGCAAGCTGCAAAT
AGGAATTTTTTCGCCAAAGTAGCTTC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024593.1|WP_099811636.1|383472_384066_+|indolepyruvate-oxidoreductase-subunit-beta	unknown	unknown	gnl|CDD|180732
NZ_CP024593.1|WP_004585237.1|360775_361060_+|NifU-family-protein	unknown	unknown	gnl|CDD|376458
NZ_CP024593.1|WP_013816402.1|378833_379346_-|isochorismatase-family-protein	unknown	unknown	gnl|CDD|238493
NZ_CP024593.1|WP_099811631.1|373002_375354_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|274576
NZ_CP024593.1|WP_099811634.1|380999_381761_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|187604
NZ_CP024593.1|WP_099811635.1|381838_383446_+|indolepyruvate-ferredoxin-oxidoreductase	unknown	unknown	gnl|CDD|274526
NZ_CP024593.1|WP_099811629.1|365561_367115_+|DUF1858-domain-containing-protein	unknown	unknown	gnl|CDD|225301
NZ_CP024593.1|WP_021666088.1|365283_365442_+|DUF1661-domain-containing-protein	unknown	unknown	gnl|CDD|285160
NZ_CP024593.1|WP_021662795.1|384461_385220_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224045
NZ_CP024593.1|WP_004585235.1|362411_363527_+|4-hydroxybutyrate-dehydrogenase	unknown	unknown	gnl|CDD|341482
NZ_CP024593.1|WP_004585230.1|368195_370571_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|274576
NZ_CP024593.1|WP_043894496.1|379378_380572_-|saccharopine-dehydrogenase-family-protein	unknown	unknown	gnl|CDD|224662
NZ_CP024593.1|WP_099811630.1|370597_372964_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|274576
NZ_CP024593.1|WP_012457730.1|361065_362361_+|acetyl-CoA-hydrolase/transferase-family-protein	unknown	unknown	gnl|CDD|223504
NZ_CP024593.1|WP_004585231.1|367443_368103_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213222
NZ_CP024593.1|WP_004585219.1|385263_386334_-|iron-ABC-transporter-permease	unknown	unknown	gnl|CDD|376439
NZ_CP024593.1|WP_012457729.1|363722_365078_+|aldehyde-dehydrogenase-family-protein	unknown	unknown	gnl|CDD|143440
NZ_CP024593.1|WP_099811633.1|377296_378631_-|TolC-family-protein	unknown	unknown	gnl|CDD|224455
NZ_CP024593.1|WP_130266966.1|380734_380899_+|DUF1661-domain-containing-protein	unknown	unknown	gnl|CDD|285160
NZ_CP024593.1|WP_099811632.1|376003_377257_-|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl|CDD|273776

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP024593.1|WP_099811636.1|383472_384066_+|indolepyruvate-oxidoreductase-subunit-beta	gnl|CDD|180732	PRK06853, PRK06853, indolepyruvate oxidoreductase subunit beta; Reviewed.	3.73575e-83
NZ_CP024593.1|WP_004585237.1|360775_361060_+|NifU-family-protein	gnl|CDD|376458	pfam01106, NifU, NifU-like domain. This is an alignment of the carboxy-terminal domain. This is the only common region between the NifU protein from nitrogen-fixing bacteria and rhodobacterial species. The biochemical function of NifU is unknown.	5.97485e-17
NZ_CP024593.1|WP_013816402.1|378833_379346_-|isochorismatase-family-protein	gnl|CDD|238493	cd01011, nicotinamidase, Nicotinamidase/pyrazinamidase (PZase). Nicotinamidase, a ubiquitous enzyme in prokaryotes, converts nicotinamide to nicotinic acid (niacin) and ammonia, which in turn can be recycled to make nicotinamide adenine dinucleotide (NAD). The same enzyme is also called pyrazinamidase, because in converts the tuberculosis drug pyrazinamide (PZA) into its active form pyrazinoic acid (POA).	2.64691e-32
NZ_CP024593.1|WP_099811631.1|373002_375354_-|FtsX-like-permease-family-protein	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	9.90344e-21
NZ_CP024593.1|WP_099811634.1|380999_381761_+|SDR-family-oxidoreductase	gnl|CDD|187604	cd05346, SDR_c5, classical (c) SDR, subgroup 5. These proteins are members of the classical SDR family, with a canonical active site tetrad and a typical Gly-rich NAD-binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	1.35086e-149
NZ_CP024593.1|WP_099811635.1|381838_383446_+|indolepyruvate-ferredoxin-oxidoreductase	gnl|CDD|274526	TIGR03336, IOR_alpha, indolepyruvate ferredoxin oxidoreductase, alpha subunit. Indolepyruvate ferredoxin oxidoreductase (IOR) is an alpha 2/beta 2 tetramer related to ketoacid oxidoreductases for pyruvate (1.2.7.1, POR), 2-ketoglutarate (1.2.7.3, KOR), and 2-oxoisovalerate (1.2.7.7, VOR). These multi-subunit enzymes typically are found in anaerobes and are inactiviated by oxygen. IOR in Pyrococcus acts in fermentation of all three aromatic amino acids, following removal of the amino group by transamination. In Methanococcus maripaludis, by contrast, IOR acts in the opposite direction, in pathways of amino acid biosynthesis from phenylacetate, indoleacetate, and p-hydroxyphenylacetate. In M. maripaludis and many other species, iorA and iorB are found next to an apparent phenylacetate-CoA ligase.	4.90445e-176
NZ_CP024593.1|WP_099811629.1|365561_367115_+|DUF1858-domain-containing-protein	gnl|CDD|225301	COG2461, COG2461, Uncharacterized conserved protein [Function unknown].	3.55366e-104
NZ_CP024593.1|WP_021666088.1|365283_365442_+|DUF1661-domain-containing-protein	gnl|CDD|285160	pfam07877, DUF1661, Protein of unknown function (DUF1661). This is a family containing bacterial proteins of unknown function. Many of the proteins in this family are hypothetical.	0.00761225
NZ_CP024593.1|WP_021662795.1|384461_385220_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224045	COG1120, FepC, ABC-type cobalamin/Fe3+-siderophores transport systems, ATPase components [Inorganic ion transport and metabolism / Coenzyme metabolism].	1.61385e-78
NZ_CP024593.1|WP_004585235.1|362411_363527_+|4-hydroxybutyrate-dehydrogenase	gnl|CDD|341482	cd14860, 4HBD_NAD, 4-hydroxybutyrate dehydrogenase, also called gamma-hydroxybutyrate dehydrogenase, catalyzes the reduction of succinic simialdehyde to 4-hydroxybutyrate in the succinic degradation pathway. 4-hydroxybutyrate dehydrogenase (4HBD) is an iron-containing (type III) NAD-dependent alcohol dehydrogenase. It plays a role in the succinate metabolism biochemical pathway. It catalyzes the reduction of succinic simialdehide to 4-hydroxybutyrate in the succinate degradation pathway This succinate degradation pathway is present in some bacteria which can use succinate as sole carbon source.	0
NZ_CP024593.1|WP_004585230.1|368195_370571_-|FtsX-like-permease-family-protein	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	1.01404e-32
NZ_CP024593.1|WP_043894496.1|379378_380572_-|saccharopine-dehydrogenase-family-protein	gnl|CDD|224662	COG1748, LYS9, Saccharopine dehydrogenase and related proteins [Amino acid transport and metabolism].	9.77501e-158
NZ_CP024593.1|WP_099811630.1|370597_372964_-|ABC-transporter-permease	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	3.83408e-44
NZ_CP024593.1|WP_012457730.1|361065_362361_+|acetyl-CoA-hydrolase/transferase-family-protein	gnl|CDD|223504	COG0427, ACH1, Acetyl-CoA hydrolase [Energy production and conversion].	1.92917e-125
NZ_CP024593.1|WP_004585231.1|367443_368103_-|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.	7.00946e-113
NZ_CP024593.1|WP_004585219.1|385263_386334_-|iron-ABC-transporter-permease	gnl|CDD|376439	pfam01032, FecCD, FecCD transport family. This is a sub-family of bacterial binding protein-dependent transport systems family. This Pfam entry contains the inner components of this multicomponent transport system.	7.40767e-68
NZ_CP024593.1|WP_012457729.1|363722_365078_+|aldehyde-dehydrogenase-family-protein	gnl|CDD|143440	cd07122, ALDH_F20_ACDH, Coenzyme A acylating aldehyde dehydrogenase (ACDH), ALDH family 20-like. Coenzyme A acylating aldehyde dehydrogenase (ACDH, EC=1.2.1.10), an NAD+ and CoA-dependent acetaldehyde dehydrogenase, functions as a single enzyme (such as the Ethanolamine utilization protein, EutE, in Salmonella typhimurium) or as part of a multifunctional enzyme to convert acetaldehyde into acetyl-CoA . The E. coli aldehyde-alcohol dehydrogenase includes the functional domains, alcohol dehydrogenase (ADH), ACDH, and pyruvate-formate-lyase deactivase; and the Entamoeba histolytica aldehyde-alcohol dehydrogenase 2 (ALDH20A1) includes the functional domains ADH and ACDH and may be critical enzymes in the fermentative pathway.	0
NZ_CP024593.1|WP_099811633.1|377296_378631_-|TolC-family-protein	gnl|CDD|224455	COG1538, TolC, Outer membrane protein [Cell envelope biogenesis, outer membrane / Intracellular trafficking and secretion].	2.09546e-39
NZ_CP024593.1|WP_130266966.1|380734_380899_+|DUF1661-domain-containing-protein	gnl|CDD|285160	pfam07877, DUF1661, Protein of unknown function (DUF1661). This is a family containing bacterial proteins of unknown function. Many of the proteins in this family are hypothetical.	0.00271467
NZ_CP024593.1|WP_099811632.1|376003_377257_-|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	gnl|CDD|273776	TIGR01730, COG0845:_Membrane-fusion_protein, RND family efflux transporter, MFP subunit. This model represents the MFP (membrane fusion protein) component of the RND family of transporters. RND refers to Resistance, Nodulation, and cell Division. It is, in part, a subfamily of pfam00529 (Pfam release 7.5) but hits substantial numbers of proteins missed by that model. The related HlyD secretion protein, for which pfam00529 is named, is outside the scope of this model. Attributed functions imply outward transport. These functions include nodulation, acriflavin resistance, heavy metal efflux, and multidrug resistance proteins. Most members of this family are found in Gram-negative bacteria. The proposed function of MFP proteins is to bring the inner and outer membranes together and enable transport to the outside of the outer membrane. Note, however, that a few members of this family are found in Gram-positive bacteria, where there is no outer membrane. [Transport and binding proteins, Unknown substrate].	1.39752e-31

Protein sequences

>NZ_CP024593.1|WP_099811631.1|373002_375354_-|FtsX-like-permease-family-protein
MRTYFKFLSRNKLYTFVTIVGFALSLIFVLLLSFYVRREQQADRIHTDYKRIYQYNVESKNNWSGFICCYPAGTLIREQVPDVEEICRISEYNDKEYIFIGADKQNGLIASHLSVESNFFTFFDGYKLLEGDPKTVLSEQNSAVISSALAARIFGNMSPIGQEISFFDFSKNKQTFRITGIMEPMPDNCHIRPAELLFYQEPKENNYNNGNYALYLKAREGADLTAQLPAVQKAVQGKDVIFAFDEKAEVKLHPLEKCYPEPLFPNEYAMMVQKGNPARTRILIAITLLVLIIAIISYINLTLAQGGSRGNEVALRRLWGSSRLAIVRRLWFESLLLIFLSTLLAVFGMFALEPVFDRLFDTHLYLARHISLTLILLLIGFMLLLSIVCAALPAWFISRFRPIEVVSGKFRRVVKSSFSQIMVISQYAITMILLSCTMVMAVQIDYMTNSDMGYDYRNKLIIDVFGLDPQIVSTMRTEIAKIPGITGIGLTRGTPLNGGNNNSSEYRGRPLSMQIFSMDSVALSLSDLKMKPNGRKADKPDRTLYLSRSAYNDFDVANLPDGVIHWGKAGEFYYCGDAPEVHFGGFKEPHPSYLFIPYPQSSAWSWSVLVGYSEGADPEQLIQSIQAVYSRITGQPYTEILRSEDIIASHSEEERSLSGFLLLFSILALVGTVMSVFAMAALRIRHKQKEIAIRKVVGAREVQILQIIGRRSLWNLLNAFAVATPVSYLVMNRWLQGYTYHADMPWWVFPASLLFVSAVAMLSMLSMAMNAASSNPVDYLKNE
>NZ_CP024593.1|WP_099811630.1|370597_372964_-|ABC-transporter-permease
MRTYFKFLSRNKLYTFVTVFGFSVSLMFVIILGIYIRNEMSVDRFHSKSDRIYMLCSEEAANWSNLAPSYIQSILPDIESYCRVANRDVYVQMPSGERLKTPILLADSTFFTLFDFRLTNGIPSQVLNDRKSAVISRDFACKLFADQDPVGQSVFLYNFPHTITGVMEGIPSNSQFKKVDIVVNYHFLSDLSGENAFRWGNCSFMAYYLLKAGTDLESKARILEETFKKEKFMWLYHQGFHKEVHFVSLPDCYFDSRVVEANLENRANNMTKVKVLTGIVLLILVIAVLNYVNMTVAQAGFRGKESAIRRLLGGSRSGVIRKLLLESLVITLLTFIAGLLLAFTFEPFFNRVLETTLDLKHQFTPSTVIAIALFVVLLSFLSGILPAWIISRFKPIEVVKGTLRYRIKSTYSKVLIIFQYTIAIALLVCSLFMIRQTHYLIHSDLGFRTRGVLWMSNTADSVPKGMLRAELEKIPGVEKVSYACGNPIRYLNNMSFTKDGVNVSTWEMVVDSVFFDFFEISPIPLTDEPVETFFDREKMRAARIIPEWGNMKMINAVRPDPETGIFTQGDDDNDEVKYRMVGRIPDLKYKPLNMEQSPLQIRPLYAREQPWVTLVRASDEADKSAVLAAVSDTYKRVTGAEDIESLWAEDIILDRYKSQTNLSQLISAFALLTVLIMVMGVFAMSLYMIKQKEKEIALRKVNGATVATILAMLNTQSLRRFGIALLIALPVSWWAMDRWLQTFAFHIRLDWWVFVVAALIVLLLSLVSTSLQSWRAACANPVDYLKNE
>NZ_CP024593.1|WP_004585230.1|368195_370571_-|FtsX-like-permease-family-protein
MLPLKLAARRLFRQGEHSISKLLTLTLGLSVSVLLLSIVIYQRSYERDFPHHDRICIVKTHGTRQSQEGDKPEELDFSQVSGGVAPAIQEEIPGVELATRTTLYGTSKMILEDNKTYETKTLLAEPAFLDMFGVELIAGVRDSALRDNMTCLISESLARKMGGDVLGKRLRPAESKSDRAITIGGVFEDLPHNSSIQADMLLPITWMPAESLNNWIGNDRYIAYVRLRPGVSPESLDEALLEMQKRHQDMEVFRKAGVELHYSLTPFNRLRLEDPTLVNMLRIQQIVAIAVLLISLLNYVLMTLASMVNRRRVAAIRKCYGAMPVQIQGTMIWETFLYLFLSLVLALLTLILFRKPMEALIETPLLHLISWRVAAALAGVLAMATFFMGWIPGYSLSRTPVMNIFRKSVAHNRLWKLGLLAVEFVAATFLFGLLAITGLQYRHMIGQDAGYKAAGLYYVPIESLDQQQLPVVIEKLKALPEVEGYTLTTALPASSGQSGDNLIDPVTDRELINVADLFYVDEHYLKVYDIELLEGKNFDVATEKDREIMLSKKAATELARLMNWKDGVIGKNIILTSFGRVVIRGVYDDLMLRRQHLSPYPEKLPSAIVYGDDWLHYLTIRLRHDDARLLHRVNGILSEADPYKETSFLSVEMELLSRFEAAKTFRNTILFGSVVAILIALIGLVGYVNTEVNRRRKELAIRKINGAGEGDILRLFLRSIFRLSLPSVLAGLFVAYLFGRNWLEKFSYRIELNGRIFLLVGLLVLLIIALAVVINLRRIARRNPVNELRYE
>NZ_CP024593.1|WP_004585231.1|367443_368103_-|ABC-transporter-ATP-binding-protein
MIEISNLTKVFRTEEIETVALDGVSLKVDKGEFIAIMGPSGCGKSTLLNILGLLDNPTSGIYKLDGAEVGNLREKDRTAVRKGNIGFVFQSFNLIEEMTVSENVELPLVYLGVKASERKERVEEALRKMSISHRAGHFPNQLSGGQQQRVAIARAVVANPKLILADEPTGNLDSKNGADVMELLRGLNREGATIVMVTHSEHDARSAGRIINLFDGKIR
>NZ_CP024593.1|WP_099811629.1|365561_367115_+|DUF1858-domain-containing-protein
MQDIKTNETFDSLDKSKLERMLDIKEAHREGHLTLEEAKERMKKEVGSISPEEFAAAEQLFKERDQDECQNEDVRTMLQLFEGLINPIRPDLPFGHPIDAYLRENDKAKELLDQADALLERTFIPNPWIELMETLMGYKLHFARKQNQLYSTLEQKGFDRPSTTMWTYDDHIRDEMNKAMSLLREKDYDSFPAAYKEMAIVLRDLMEKEELILYPTSLKLISDKEFEEMKHGDREIGFFLIDMPELDAPAKQSKEAHGQSFMAELGALLAKHGMGTGGQDDKAILDVAEGKLTLEQINLLFRHLPVDISFVDENELVCFYTDTKHRVFPRSKGVIGREVRNCHPPKSVHIVEEIIDKFRRGEQDRAEFWINKPGVFIYIVYVAIRDADGRFRGVMEMMQDCTRIRSLEGSRTLLTWDEEQSPAQGSKESESDTVGEDGIRPDTKLKSLLQRYPQLMDDLPTISSKFTLLRSPMAKVILPVATIKMMSERADIPSDMLIGKLESLIASYNKPDRSEEK
>NZ_CP024593.1|WP_021666088.1|365283_365442_+|DUF1661-domain-containing-protein
MNFLLLAWEKKKSETKTKKISRLLFTKHRPQSEHFRLVSCLRRNEHMHFFPR
>NZ_CP024593.1|WP_012457729.1|363722_365078_+|aldehyde-dehydrogenase-family-protein
MEIKEMVSLARKAQKEYQATHNQEAVDNICRAAAKVIYENAAILAREAVDETGMGVYEHKVAKNQGKSKGVWYNLHNKKSVGILNIDERTGMIEIAKPIGVVGAVTPTTNPIVTPMSNIIFALKTCNAIIIAPHPRSKKCSAHAVRLIKEAIAPFNVPEGMVQIIEEPSIEKTQELMGAVDVVVATGGMGMVKSAYSSGKPSFGVGAGNVQVIVDSNIDFEAAAEKIITGRAFDNGIICSGEQSIIYNEADKEAVFTAFRNHGAYFCDEAEGDRARAAIFENGAIAKDVVGQSVAFIAKKANINIPEGTRILVVEARGVGAEDVICKEKMCPVMCALSYKHFEEGVEIARTNLANEGNGHTCAIHSNNQAHIILAGSELTVSRIVVNAPSATTAGGHIQNGLAVTNTLGCGSWGNNSISENFTYKHLLNISRIAPLNSSIHIPDDKEIWEL
>NZ_CP024593.1|WP_004585235.1|362411_363527_+|4-hydroxybutyrate-dehydrogenase
MQLFKLKSVTHHFDTFAEFAKEFCLGERDLVITNEFIYEPYMKACQLPCHFVMQEKYGQGEPSDEMMNNILADIRNIQFDRVIGIGGGTVIDISKLFVLKGLNDVLDAFDRKIPLIKEKELIIVPTTCGTGSEVTNISIAEIKSRHTKMGLADDAIVADHAIIIPELLKSLPFHFYACSAIDALIHAIESYVSPKASPYSRLFSEAAWDIILEVFKKIAEHGPEYRFEKLGEMIMASNYAGIAFGNAGVGAVHALSYPLGGNYHVPHGEANYQFFTEVFKVYQKKNPFGYIVELNWKLSKILNCQPEYVYPKLDELLGCLLTKKPLHEYGMKDEEVRGFAESVLKTQQRLLANNYVELTVDEIEGIYRRLY
>NZ_CP024593.1|WP_012457730.1|361065_362361_+|acetyl-CoA-hydrolase/transferase-family-protein
MKDVLAEYASRIVSAEEAVKHIKNGERVALSHAAGVPQSCVDALVQQADLFQNVEIYHMLCLGEGKYMAPEMAPHFRHITNFVGGNSRKAVEENRADFIPVFFYEVPSMIRKDILHIDVAIVQLSMPDENGYCSFGVSCDYSKPAAESAHLVIGEINRQMPYVHGDNLIHISKLDYIVMADYPIYSLAKPKIGEVEEAIGRNCAELIEDGATLQLGIGAIPDAALLFLKDKKDLGIHTEMFSDGVVELVRSGVITGKKKTLHPGKMVATFLMGSEDVYHFIDKNPDVELYPVDYVNDPRVIAQNDNMVSINSCIEIDLMGQVVSECIGSKQFSGTGGQVDYVRGASWSKNGKSIMAIPSTAKNGTASRIVPIIAEGAAVTTLRNEVDYVVTEYGIAQLKGKSLRQRAEALIAIAHPDFREELTEHLRKRFG
>NZ_CP024593.1|WP_004585237.1|360775_361060_+|NifU-family-protein
MTEEIVELVLRERISPLLRSHGGDLSLSQIKDKTVFVRFSGACRFCPAAHETVEKIVQAMIREYFKDDNIDVILENSVSDDLLEQAKNILRKPK
>NZ_CP024593.1|WP_099811632.1|376003_377257_-|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit
MDRKIEKKKTLIPRKYYPYAGGAIVILALAAWAVFGNHSTKFRAERARISIDSVRRGEFNDYVRINGQVQPINSIQISAVEGGMVAEKTVEEGAMVHKGDIIVRLTNPMLNLNILDSEAQLAEKQNFLRNTQVTMEQDRLNLKRESLNLRLDIERKKRKAEQYARLYKEKLCSREEYLQAGEDYQYAVEGSGLVMERQRQDSLYRGIQVRQMEESLHNMRRNLEMVRARVEDLNVKAPADGQLGLLDVEIGQTVGSGSRIGQINVLSDYKVEAMIDEHYIDRVKAGLAASFERQGRDFSLRVRKVYPEVRDKQFRTDFVFDGERPDNIRTGQTYYINLRLGQPSEAIMIPRGAFYQNTGGRWIFVVTPDGKRAVRRDITIARQNPQYYEVTSGLHAGEMVITSSYDMFGDAEEIILN
>NZ_CP024593.1|WP_099811633.1|377296_378631_-|TolC-family-protein
MRFQHYLICTAAVAVLAANPLTGQSNMTLEECIDYARRHSSAVALSATELEQSKADYLQAVGNFLPRVSAGTGASWNFGRGLDAETNTYTDINSFNNSYSIHATMTLFDGLQSVYRLRMAHARREASRLSVREQQELAALGTTEAYYDLVYARQMQELAMQKYEESSRLHRQTARMEELGMKSRPDVLEMQSRMAGDRLALTQADNQYIIALIRLKEKMNFPIDDELVVDDMPADSLSADMAESDSSAGVFARAAHHHPVLLRAKLDEQAATDRLRAARGAFLPSVSVSGGWNTGFSRFLNGSDYTPFSEQFRNRRGEYVSLNLSIPIFSGFSLVSNLRQARAERRAASVRRGEAERRLYSEIAQAMADRDAALASYRQAKEHADAMQAAYEAVLQRYEEGLNTAIDLTTQANRLLDARVQRLRAAMTYRLKCKLIAYYGCLSD
>NZ_CP024593.1|WP_013816402.1|378833_379346_-|isochorismatase-family-protein
MVLLIVDPQVDFVSGSLAVEGAPKAMKALAEYMAAHRKEIKSIVVTMDQHPADHCSFVAQGGQWPSHCVRYTVGAAIEPCIAEALAACSAEGIPVEMIEKATTQERDAYSAFETEVPDSLRSTERIVVAGIAGDYCVRQSVLDLERHGLGERIELLKEGIAYIAEEENRP
>NZ_CP024593.1|WP_043894496.1|379378_380572_-|saccharopine-dehydrogenase-family-protein
MGKVLIIGAGGVGTVVAKKVAMNTDVFTEIMLASRTRSKCDKIASEIKNVRIQTAQVDADNVEELVALFESFKPELVINVALPYQDLTIMDACLRCGVNYLDTANYEPLDEAKYEYSWQWAYQDRFRKAGLTAILGCGFDPGVTSVYTAYAAKHHFDEIHYLDIVDCNGGDHHKAFATNFNPEINIREITQKGKYWENGRWIETEPQEIHKTLTYPSIGERESYLLYHEELESLVKNFPTIKRARFWMTFGQEYLTHLRVMQNIGMTRIDPIMYNGVEIVPIQFLKAVLPNPGELGENYTGETSIGCRIRGIRDGKEHTYYIWNNCSHEVAYKETGTQGVSYTTGVPATVGAMMFMKGIWRKPGVFNVEEFDPDPFLEEVAKQGLPWHEKHDIDLEL
>NZ_CP024593.1|WP_130266966.1|380734_380899_+|DUF1661-domain-containing-protein
MPRHKTWCVNFFVLVREVKNSRATTKKFSRHFVQKTRATIRSFAVRISDKTDPD
>NZ_CP024593.1|WP_099811634.1|380999_381761_+|SDR-family-oxidoreductase
MNPIALITGATSGIGAASARRLASLGYNLIITGRRSERLQNIADEIRAEYPVEILPLSFDVRNREEVEAHLGNLPDPWQAVSVLVNNAGLAAGLDPIQSGDIEDWERMIDTNIKGLLYVTRTISPGMIARGAGHIINIGSIAGKEVYSNGNVYCATKHAVDALSKAMRIDMLPYGIKVTQICPGAVETEFSLVRFHDDQAKADAVYKGFTPLCANDIAECIAAVLNLPDNICINDMVVMPKAQAGSGHFFKQV
>NZ_CP024593.1|WP_099811635.1|381838_383446_+|indolepyruvate-ferredoxin-oxidoreductase
MQKQLLLGVEAIAQAALDAGISGVYAYPGTPSTEITEHIQNSRMAKERNVHREWAANEKTAMESALGMSYAGKRALVCMKHVGMNVAADCFMNAAITGANGGMVIVAADDPSMHSSQNEQDSRVYGQFAMIPVMEPSNQQEAYDMTRLAFDLSERLGTPVMIRITTRLAHSRAGVVQTEPIGENELHLPEDKRQYVLLPGIAKKRYRILLDKQTDFVRESENSPYTEYVDAADKSKGIVACGIAYNYLMEAFKAQVPYPVLKVTQYPIPHKQMERLLNECGDIVVMEEGYPVVEQLLKGFPGLERIKGRLDGTLPRDGELNPDHVAKAFNIPVVEGEPIPDLVAARPPALCKGCSHRDVYDALNEVLTEYPNGRVFSDIGCYTLGALPPYEAINSCVDMGASITMAKGAADAGLFPAVSVIGDSTFTHSGITGLLDAINENSNITVIISDNESISMTGGQRSSAYGKVEAICRGIGVDPDHIKELLPVPKNHDELCSIIREEINYEGVSVIIPRRVCIQKHARDAKAAKRAKAKE
>NZ_CP024593.1|WP_099811636.1|383472_384066_+|indolepyruvate-oxidoreductase-subunit-beta
MKTDIILAGVGGQGILSIAAAIGSAALTNNLYLKQAETHGMSQRGGDVQSFLRLSDAPIYSDLIPIGGADLILSVEPMEALRYLPYLKPDGYVVTNTVPFINIPDYPETTSVISKIESLPHHVLIDADSIARDEVGNVRASNFVMLGAASPFIEIPFDYLAGGIEAIFSRKGQEVVDMNLKALNAGREFALRYAAGK
>NZ_CP024593.1|WP_021662795.1|384461_385220_-|ABC-transporter-ATP-binding-protein
MEKSIELSRLAIGYRTKSGDRIVASGLDAHLHAGQLTALLGVNGAGKSTLMRTMAGFMKPLSGQIHLLGRSLDSYKEIEIAKRIGVVLTDNCRIAGMTAGELVALGRSPYTGFWGRLQKGDRKLVAEAVERVGIAPLINRELTTLSDGERQKVVIAKALAQQTPIIFLDEPTAFLDYPSKMELLHLLHSLAHDTGRTIFLSTHDLDAILPMADRVWLLDKERSFREGTPASLASALEDYFGYTHPSPTLEPV
>NZ_CP024593.1|WP_004585219.1|385263_386334_-|iron-ABC-transporter-permease
MTSVSHLRTISVAGILAALGGAVLILFGVNLFLGSVAIPMSEIFRHLFSDRPEGGEALVHYNILWKSRLPEALTAAFAGAGLSVSGLQMQTVFRNPLAGPSVLGISSGASLGVALVVLLSGSLGGVALSSLGYMGEVAMNIAAAVGSLAVMGLIVFVSTKVRSHVTLLIIGVMIGYVATAVIGVFKFFSIEEDIRAYVIWGLGSFSRATDSQLSFFAILMLIFIPAGMLLVKQLNLLLLGESYARNLGLNTRRARLLVISSAGLLIAAVTAYCGPIGFLGMAVPHLARVIFHTSDHRILMPATCLIGSALALFCNIIARMPGFEGALPVNSVTALVGAPIIVTVLFRRRRFKEETD

Crispr_ID: NZ_CP024593_3

• CRISPR_ID: NZ_CP024593_3
• CRISPR_location: 739528-739894
• Repeat_type: VI-B2
• Spacer_info: 5 spacers
• Cas_protein_info: Csx28,cas13b

Consensus repeat of NZ_CP024593_3

Consensus_repeat	Method
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACT	PILER-CR
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAAC	CRISPRCasFinder
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACT	CRT

spacers of NZ_CP024593_3

>3.1|739565|29|NZ_CP024593|PILER-CR,CRT
CAATCAGACGAGTTAATAGAACACTAAAG
>3.2|739631|29|NZ_CP024593|PILER-CR,CRT
TTCTGAAGACATGTTTATCGACGTCGTAG
>3.3|739697|29|NZ_CP024593|PILER-CR,CRT
TTATTGGTGATGATAAACAACTTCCTCCT
>3.4|739763|29|NZ_CP024593|PILER-CR,CRT
TATAAAAGCCACTGAAAAATATGTAAAAG
>3.5|739829|29|NZ_CP024593|PILER-CR,CRT
GATGGACGATGATACGGCCTATTTCGGTT
>3.6|739564|30|NZ_CP024593|CRISPRCasFinder
TCAATCAGACGAGTTAATAGAACACTAAAG
>3.7|739630|30|NZ_CP024593|CRISPRCasFinder
CTTCTGAAGACATGTTTATCGACGTCGTAG
>3.8|739696|30|NZ_CP024593|CRISPRCasFinder
TTTATTGGTGATGATAAACAACTTCCTCCT
>3.9|739762|30|NZ_CP024593|CRISPRCasFinder
TTATAAAAGCCACTGAAAAATATGTAAAAG
>3.10|739828|30|NZ_CP024593|CRISPRCasFinder
TGATGGACGATGATACGGCCTATTTCGGTT

CRISPR arrays and Neighbor proteins around NZ_CP024593_3

CRISPR arrays

The CRISPR arrays of NZ_CP024593_3

>merge|NZ_CP024593|3|739528-739894|PILER-CR,CRISPRCasFinder,CRT
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACTCAATCAGACGAGTTAATAGAACACTAAAGGTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACCTTCTGAAGACATGTTTATCGACGTCGTAGGTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACTTTATTGGTGATGATAAACAACTTCCTCCTGTTGTGTGTGCCCTTCGAATAGAGGGTAGATCCAACTTATAAAAGCCACTGAAAAATATGTAAAAGGTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACTGATGGACGATGATACGGCCTATTTCGGTTGTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACT

>NZ_CP024593|3|1|739528-739894|PILER-CR
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACT	CAATCAGACGAGTTAATAGAACACTAAAG
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACC	TTCTGAAGACATGTTTATCGACGTCGTAG
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACT	TTATTGGTGATGATAAACAACTTCCTCCT
GTTGTGTGTGCCCTTCGAATAGAGGGTAGATCCAACT	TATAAAAGCCACTGAAAAATATGTAAAAG
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACT	GATGGACGATGATACGGCCTATTTCGGTT
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACT

>NZ_CP024593|3|3|739528-739893|CRISPRCasFinder
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAAC	TCAATCAGACGAGTTAATAGAACACTAAAG
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAAC	CTTCTGAAGACATGTTTATCGACGTCGTAG
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAAC	TTTATTGGTGATGATAAACAACTTCCTCCT
GTTGTGTGTGCCCTTCGAATAGAGGGTAGATCCAAC	TTATAAAAGCCACTGAAAAATATGTAAAAG
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAAC	TGATGGACGATGATACGGCCTATTTCGGTT
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAAC

>NZ_CP024593|3|1|739528-739894|CRT
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACT	CAATCAGACGAGTTAATAGAACACTAAAG
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACC	TTCTGAAGACATGTTTATCGACGTCGTAG
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACT	TTATTGGTGATGATAAACAACTTCCTCCT
GTTGTGTGTGCCCTTCGAATAGAGGGTAGATCCAACT	TATAAAAGCCACTGAAAAATATGTAAAAG
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACT	GATGGACGATGATACGGCCTATTTCGGTT
GTTGTGTGTACCCTTCGAATAGAGGGTAGATCCAACT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024593.1|WP_099811718.1|731400_733497_-|ATP-dependent-DNA-helicase-RecG	unknown	unknown	gnl|CDD|236794
NZ_CP024593.1|WP_099811723.1|749726_751691_-|transcription-termination-factor-Rho	unknown	unknown	gnl|CDD|236490
NZ_CP024593.1|WP_005873799.1|729081_730536_+|hypothetical-protein	unknown	unknown	gnl|CDD|380191
NZ_CP024593.1|WP_099811722.1|748591_749500_-|DMT-family-transporter	unknown	unknown	gnl|CDD|273359
NZ_CP024593.1|WP_012458402.1|726826_727012_+|DUF1661-domain-containing-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_004584821.1|744466_745036_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_021664583.1|752917_753913_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_004584818.1|747621_748581_+|glycosyltransferase-family-2-protein	unknown	unknown	gnl|CDD|133030
NZ_CP024593.1|WP_004584819.1|746079_747594_+|glycosyltransferase-family-39-protein	unknown	unknown	gnl|CDD|224720
NZ_CP024593.1|WP_021664579.1|745052_745955_+|tRNA-(adenosine(37)-N6)-dimethylallyltransferase-MiaA	unknown	unknown	gnl|CDD|234626
NZ_CP024593.1|WP_012458422.1|752366_752885_+|DUF4496-domain-containing-protein	unknown	unknown	gnl|CDD|273496
NZ_CP024593.1|WP_004584826.1|737511_738711_+|methionine-gamma-lyase	unknown	unknown	gnl|CDD|168478
NZ_CP024593.1|WP_099811719.1|733539_734568_-|UDP-glucose-4-epimerase-GalE	unknown	unknown	gnl|CDD|187558
NZ_CP024593.1|WP_077083539.1|734577_735183_-|YihA-family-ribosome-biogenesis-GTP-binding-protein	unknown	unknown	gnl|CDD|234770
NZ_CP024593.1|WP_099811720.1|735879_737349_+|metallophosphoesterase-family-protein	unknown	unknown	gnl|CDD|277318
NZ_CP024593.1|WP_099811717.1|727076_728519_-|exo-alpha-sialidase	unknown	unknown	gnl|CDD|271234
NZ_CP024593.1|WP_004584828.1|735283_735877_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_005873802.1|730630_731401_-|HAD-IA-family-hydrolase	unknown	unknown	gnl|CDD|223710
NZ_CP024593.1|WP_021665928.1|740101_740647_-|hypothetical-protein	Csx28	-	unknown
NZ_CP024593.1|WP_099811721.1|740651_744179_-|hypothetical-protein	cas13b	cas13b_CAS_V-B1	gnl|CDD|380475

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP024593.1|WP_021665928.1|740101_740647_-|hypothetical-protein	Csx28	-	6.8e-96	314.1	1.2
NZ_CP024593.1|WP_099811721.1|740651_744179_-|hypothetical-protein	cas13b	cas13b_CAS_V-B1	0	1392.3	21.8

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP024593.1|WP_099811718.1|731400_733497_-|ATP-dependent-DNA-helicase-RecG	gnl|CDD|236794	PRK10917, PRK10917, ATP-dependent DNA helicase RecG; Provisional.	0
NZ_CP024593.1|WP_099811723.1|749726_751691_-|transcription-termination-factor-Rho	gnl|CDD|236490	PRK09376, rho, transcription termination factor Rho; Provisional.	0
NZ_CP024593.1|WP_005873799.1|729081_730536_+|hypothetical-protein	gnl|CDD|380191	NF033187, internalin_J, class 1 internalin InlJ. Internalins, as found in the intracellular human pathogen Listeria monocytogenes, are paralogous surface-anchored proteins with an N-terminal signal peptide, leucine-rich repeats, and a C-terminal LPXTG processing and cell surface anchoring site. See PMID:17764999 for a general discussion of internalins. Members of this family are internalin J (InlJ).	1.30429e-35
NZ_CP024593.1|WP_099811722.1|748591_749500_-|DMT-family-transporter	gnl|CDD|273359	TIGR00950, Uncharacterized_inner_membrane_transporter_YicL, Carboxylate/Amino Acid/Amine Transporter. [Transport and binding proteins, Amino acids, peptides and amines].	2.17421e-12
NZ_CP024593.1|WP_004584818.1|747621_748581_+|glycosyltransferase-family-2-protein	gnl|CDD|133030	cd04187, DPM1_like_bac, Bacterial DPM1_like enzymes are related to eukaryotic DPM1. A family of bacterial enzymes related to eukaryotic DPM1; Although the mechanism of eukaryotic enzyme is well studied, the mechanism of the bacterial enzymes is not well understood. The eukaryotic DPM1 is the catalytic subunit of eukaryotic Dolichol-phosphate mannose (DPM) synthase. DPM synthase is required for synthesis of the glycosylphosphatidylinositol (GPI) anchor, N-glycan precursor, protein O-mannose, and C-mannose. The enzyme has three subunits, DPM1, DPM2 and DPM3. DPM is synthesized from dolichol phosphate and GDP-Man on the cytosolic surface of the ER membrane by DPM synthase and then is flipped onto the luminal side and used as a donor substrate. This protein family belongs to Glycosyltransferase 2 superfamily.	3.12682e-98
NZ_CP024593.1|WP_012458422.1|752366_752885_+|DUF4496-domain-containing-protein	gnl|CDD|273496	TIGR01201, HU_rel, DNA-binding protein, histone-like, putative. This model describes a set of proteins related to but longer than DNA-binding protein HU. Its distinctive domain architecture compared to HU and related histone-like DNA-binding proteins justifies the designation as superfamily. Members include, so far, one from Bacteroides fragilis, a gut bacterium, and ten from Porphyromonas gingivalis, an oral anaerobe. [DNA metabolism, Chromosome-associated proteins].	1.34591e-52
NZ_CP024593.1|WP_021664579.1|745052_745955_+|tRNA-(adenosine(37)-N6)-dimethylallyltransferase-MiaA	gnl|CDD|234626	PRK00091, miaA, tRNA delta(2)-isopentenylpyrophosphate transferase; Reviewed.	4.99359e-126
NZ_CP024593.1|WP_004584826.1|737511_738711_+|methionine-gamma-lyase	gnl|CDD|168478	PRK06234, PRK06234, methionine gamma-lyase; Provisional.	0
NZ_CP024593.1|WP_099811719.1|733539_734568_-|UDP-glucose-4-epimerase-GalE	gnl|CDD|187558	cd05247, UDP_G4E_1_SDR_e, UDP-glucose 4 epimerase, subgroup 1, extended (e) SDRs. UDP-glucose 4 epimerase (aka UDP-galactose-4-epimerase), is a homodimeric extended SDR. It catalyzes the NAD-dependent conversion of UDP-galactose to UDP-glucose, the final step in Leloir galactose synthesis. This subgroup has the characteristic active site tetrad and NAD-binding motif of the extended SDRs. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	2.63252e-179
NZ_CP024593.1|WP_099811720.1|735879_737349_+|metallophosphoesterase-family-protein	gnl|CDD|277318	cd00839, MPP_PAPs, purple acid phosphatases of the metallophosphatase superfamily, metallophosphatase domain. Purple acid phosphatases (PAPs) belong to a diverse family of binuclear metallohydrolases that have been identified and characterized in plants, animals, and fungi. PAPs contain a binuclear metal center and their characteristic pink or purple color derives from a charge-transfer transition between a tyrosine residue and a chromophoric ferric ion within the binuclear center. PAPs catalyze the hydrolysis of a wide range of activated phosphoric acid mono- and di-esters and anhydrides. PAPs are distinguished from the other phosphatases by their insensitivity to L-(+) tartrate inhibition and are therefore also known as tartrate resistant acid phosphatases (TRAPs). While only a few copies of PAP-like genes are present in mammalian and fungal genomes, multiple copies are present in plant genomes. PAPs belong to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	3.25097e-14
NZ_CP024593.1|WP_099811717.1|727076_728519_-|exo-alpha-sialidase	gnl|CDD|271234	cd15482, Sialidase_non-viral, Non-viral sialidases. Sialidases or neuraminidases function to bind and hydrolyze terminal sialic acid residues from various glycoconjugates, they play vital roles in pathogenesis, bacterial nutrition and cellular interactions. They have a six-bladed, beta-propeller fold with the non-viral sialidases containing 2-5 Asp-box motifs (most commonly Ser/Thr-X-Asp-[X]-Gly-X-Thr- Trp/Phe). This CD includes eubacterial and eukaryotic sialidases.	2.27688e-91
NZ_CP024593.1|WP_004584819.1|746079_747594_+|glycosyltransferase-family-39-protein	gnl|CDD|224720	COG1807, ArnT, 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family [Cell envelope biogenesis, outer membrane].	8.82534e-34
NZ_CP024593.1|WP_005873802.1|730630_731401_-|HAD-IA-family-hydrolase	gnl|CDD|223710	COG0637, COG0637, Predicted phosphatase/phosphohexomutase [General function prediction only].	1.15004e-37
NZ_CP024593.1|WP_077083539.1|734577_735183_-|YihA-family-ribosome-biogenesis-GTP-binding-protein	gnl|CDD|234770	PRK00454, engB, GTP-binding protein YsxC; Reviewed.	3.4289e-97
NZ_CP024593.1|WP_099811721.1|740651_744179_-|hypothetical-protein	gnl|CDD|380475	cd20477, Cas13b_Pb-like, Class 2 type VI-B CRISPR-associated RNA-guided ribonuclease Cas13b from Prevotella buccae and similar Cas13b proteins. CRISPR-Cas (clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins) adaptive immune systems defend microbes against foreign nucleic acids via RNA-guided endonucleases. These systems are divided into two classes: class 1 systems utilize multiple Cas proteins and CRISPR RNA (crRNA) to form an effector complex while class 2 systems employ a large, single effector with crRNA to mediate interference. Class 2 type VI CRISPR-Cas13 systems use a single enzyme to target RNA using a programmable crRNA guide and are divided into four subtypes based on the identity of the Cas13 protein (Cas13a-d). The Cas13 proteins are capable of both pre-crRNA processing and target RNA cleavage, which protect the host from phage attacks. Once bound to a target RNA, their non-specific RNase activity is activated. Cas13b has many distinctive features compared to the other Cas13 proteins, including the lack of significant sequence similarity, disparate crRNA repeat region, and double-sided protospacer flanking sequence (PFS)-dependent target RNA cleavage.	0

Protein sequences

>NZ_CP024593.1|WP_004584826.1|737511_738711_+|methionine-gamma-lyase
MKKEDLMRSGFATRAIHGGAIENAFGCLATPIYQTSTFVFDSAEQGGRRFAGEEDGYIYTRLGNPNCTQVEEKLAMLEGGEAAASASSGIGAISSAIWVCVKAGDHIVAGKTLYGCTFAFLTHGLSRYGVEVTLVDTRHPEEVEAAIRPNTKLVYLETPANPNMYLTDIKAVCDIAHKHEGVRVMVDNTYCTPYICRPLELGADIVVHSATKYLNGHGDVIAGFVVGKEDYIKEVKLVGVKDLTGANMSPFDAYLISRGMKTLQIRMEQHCRNAQTVAEFLEKHPAVEAVYFPGLPSFPQYELAKKQMALPGAMIAFEVKGGCEAGKKLMNSLHLCSLAVSLGDTETLIQHPASMTHSPYTPEERAASDISEGLVRLSVGLENVEDIIADLKHGLDSLI
>NZ_CP024593.1|WP_099811720.1|735879_737349_+|metallophosphoesterase-family-protein
MRKKRSNPYYKVSRRKFSKRNSGRRYSRKRRRNGRRWGLMISLLLLVALGIWIAKRYRAWFVSPAEVAYTVPHTIDRLTLTPGEDFLTQRTVSWRCDTLPQDSWLDYRSPDGADADTLLISLPAEGKEVLTRAGRNYYYHAKINGLKPGRTYTYRVKTGEQTSPWYRFSIPDSSAATDFIYIGDVQDPGNGGSQALLQRLRTLHPNPDFLALGGDQIEGPTNFYWEVWHRVIGDWTASTPVIAATGNHEYIKGLKRQLDPRWVPQYNYPANGPKGFERRSYYIDFPHMRLIVMDTNDIQWPASVFNHRTWLKNALETTVQPWKVVMFHHGVYSVRQGRMNPIIRYGFRSILEEGGADLVLQGHDHAYSRITTKTESGTKTTPVYIISSASPKHYRNGFSEQHDRIGSGLYLYQTIHVTQGEIRYRSTTFDNRPYDDLHLKKQGGRTTVKDNAEDWKEIFAFDNFADSKKGRKKRADYRQAAKERAAGHR
>NZ_CP024593.1|WP_004584828.1|735283_735877_+|hypothetical-protein
MNKSLIILIYTLVWVLLIVLQSLALESANPGTPSFWNTPSAYYSVWIVDAYIIALYYINYFLIAPFMIKRHLFRPYIVLSLALGGIGMLLPVVFHHAWQWTIPGTSEGQMPLYGEGFIASIAAIAVGLSVRGVREWVRLARRNTNLEIALKNKSIAYDRAEARLRSLEQPVSFHNPGTGAKAENAPSSTPVSPQTNE
>NZ_CP024593.1|WP_077083539.1|734577_735183_-|YihA-family-ribosome-biogenesis-GTP-binding-protein
MEIKKAAFVISNTDVCKCPDTRLPEYAFIGRSNVGKSSLINMLTGQKGLAMTSQKPGKTQLINHFIIDDSWYLVDLPGYGYARLGASNRESLRRIIETYILCREQLSSLFVLIDCRHEPQKIDLEFLQWLGENGIPFGIVFTKADKLSFSRLKENTEAYKQKLLETWEELPPVFITSSEKKTGKEELLDYIDSINQELATK
>NZ_CP024593.1|WP_099811719.1|733539_734568_-|UDP-glucose-4-epimerase-GalE
MKQKILVTGGTGYIGSHTTVELQQVGYRVVSVDNFSNSNAAVLDGIARITGVRPDFYEADCNDTEAMERVFTAHPDIAGVIHFAASKAVGESVQKPLLYYRNNILSLLNILELMERFGTRGIVFSSSCTVYGQPEVLPVTEEAPIQEALSPYGNTKQINEEIIRDAIHAGAGYKAILLRYFNPIGAHPTANIGELPNGVPQNLIPYLTQTAAGIRAELSVFGDDYDTPDGSCIRDYIYVVDLAKAHVAAIERMLNEEKASDSLEVFNIGTGRGVSVLELIRTFERVAGVAVPHRIVGRREGDIEQVWAEPKKANEVLGWKALESLEDTLLSAWRWQQRLSEK
>NZ_CP024593.1|WP_099811718.1|731400_733497_-|ATP-dependent-DNA-helicase-RecG
MDILSTKITYLTGVGPKRAEVLKEEIEVRTYLDLLHYFPFRYVDRSRFYAIREIRSDMPYIQLRGVLRNFSEVGEGRRKRLTATFSDGTGSIELVWFKGIKYIRDKLQEGRRYIVFGKPVFFASGYNIAHPEIDAEEKAEQVAGGLTPIYHTTERMKSMGLGSKQLQQLLYVLLNQVSATLTETLPPYILSSYGFVSYQEAIRQIHFPQGVAQLEAARTRLKFEELFYVQLHLIGSKLERKARFQGIVFAQVGALFNTFYKEHLLFELTGAQKRVVREIRQDTLSGHQMNRLVQGDVGSGKTLVALLSMLLALDNGCQACLMAPTEILARQHHHTLSELLRPLGIEVGLLIGSCTARQRERLLPRLADGSLSIVVGTHALLEQGVAFRRLGMAVIDEQHRFGVQQRARLWEKNLDTLPHILIMSATPIPRTLAMTLYGDLDISIIDELPPGRKPIQTLHHFDNDMAPVFRFLRSQLAAGRQVYVVYPMIEGSETTDLKNLEDGFELFSSIFPDEGVTMVHGKMKAKEKEARMADFVSGRSRILLATTVIEVGVNVPNATVMVVENADRFGLSQLHQLRGRVGRGGEQSYCILITGTKTGEDSRRRIQVMVETNDGFEIAEEDMRLRGFGDLEGTRQSGRQISLRIANPARDTELIALSRSIAEQLLERDPELRHPDNQMLALRLNKLFPKEEDWSVIS
>NZ_CP024593.1|WP_005873802.1|730630_731401_-|HAD-IA-family-hydrolase
MEKKESMDYNNITEALQAFRTEKAYRHAPLRSCFFDMDGVLFDSMPAHARSWVEAAGECGIAAEPLDFYRWEGQKGSDTIKILFERGYGRLPTEKEIADMYGRKSQLFALYNSGNVIDDAPALVSDVCDRGLRIMLVTGSSQTDILQRLQRSYGDNFSPANMVTGADVHRGKPHPEPYLKALECVGMSPSEAFVVENAPLGVRAAVDAGIFTIAVNTGCLPDADLWDAGASLVLPSMAVLRSLLGELLTESLSSSA
>NZ_CP024593.1|WP_005873799.1|729081_730536_+|hypothetical-protein
MKRKPLFSALVILSGFFGSVHPASAQKVPAPVDGERIIMELSEADVECTIKIEAEDGYANDIWADLNGNGKYDSGERLDSGEFRDVEFRQTKAIVYGKMAKFLFRGSSAGDYGATFIDISNCTGLTAFDCFANLLTELDLSKANGLTFVNCGKNQLTKLDLPANADIETLNCSKNKITSLNLSTYTKLKELYVGDNGLTALDLSANTLLEELVYSNNEVTTINLSANTNLKSLYCINNKMTGLDVAANKELKILHCNNNQLTALNLSANTKLTTLSFFNNELTNIDLSDNTALEWLFCNGNKLTKLDVSANANLIALQCSNNQLTALDLSKTPKLTTLNCYSNRIKDTAMRALIESLPTITEGEGRFVPYNDDEGGEEENVCTTEHVEMAKAKNWKVLTSWGEPFPGITALISIEGESEYSVYAQDGILYLSGMEQGLPVQVYTVGGSMMYSSVASGSAMEIQLPRGAAYVVRIGSHAIKTAMP
>NZ_CP024593.1|WP_099811717.1|727076_728519_-|exo-alpha-sialidase
MYRTLVKVALSESLPPDAKQIRIGFSLPKETEEKVTALYLLVSDSLAVRDLPDYKGRVSYDSFPISKEDRTTALSADSVAGRRFFYLAADIGPVASFSRSDTLTARVEEVAVDGRPLPLKELSPASRRLYRGYEALFVPGDGGSRNYRIPAILKTANGTLIAMADRRKYNQTDLPEDIDIVMRRSTDGGKSWSDPRIIVQGEGRNHGFGDVALVQTQAGKLLMIFVGGVGLWQSTPDRPQRTYISESRDEGLTWSSPRDITHFIFGKDCADPGRSRWLASFCASGQGLVLPSGRITFVAAIRESGQEYVLNNYVLYSDDEGGTWQLSDCAYHRGDEAKLSLMPDGRVLMSVRNQGRQESRQRFFALSSDDGLTWERAKQFEDIHDPGCNGAMLQVKRNGRDQVLHSLPLGPDGRRDGAVYLFDHTSGRWSAPVVVNSGSSAYSDMTLLADGTIGYFVEEDDEISLVFIRFVLDDLFDARQ
>NZ_CP024593.1|WP_012458402.1|726826_727012_+|DUF1661-domain-containing-protein
MPEFSCLQFGKTWRVNFFALAREVKKSRTKTKKFRHHLLQKRRAAIRGFSARIGGIAVDGY
>NZ_CP024593.1|WP_021665928.1|740101_740647_-|hypothetical-protein
MITMTICWTPICVQLLKLSGIFIAAYLAYRYAVRKLSKESIENIERCKYQAVLEAHRSFYKLLRFTTDTENADSILVWQKAKGGGAKTYYFRPACIRGFLSELTDEFYKNGNGIFLSKEIISRIFEYRSIVYGLLLSERQNSDERVVMNKPETAERMISIHQELTQTVREAIALKKRTLNF
>NZ_CP024593.1|WP_099811721.1|740651_744179_-|hypothetical-protein
MTEQNEKPYNGTYYTLEDKHFWAAFFNLARHNAYITLAHIDRQLAYSKADITNDEDILFFKGQWKNLDNDLERKARLRSLILKHFSFLEGAAYGKKLFESQSSGNKSSKKKELTKKEKEELQANALSLDNLKSILFDFLQKLKDFRNYYSHYRHPESSELPLFDGNMLQRLYNVFDVSVQRVKRDHEHNDKVDPHRHFNHLVRKGKKDRCGNNDNPFFKHHFVDREEKVTEAGLLFFVSLFLEKRDAIWMQKKIRGFKGGTEAYQQMTNEVFCRSRISLPKLKLESLRTDDWMLLDMLNELVRCPKSLYDRLREEDRARFRVPVDILSDEDDTDGTEEDPFKNTLVRHQDRFPYFALRYFDLKKVFTSLRFHIDLGTYHFAIYKKNIGEQPEDRHLTRNLYGFGRIQDFAEEHRPEEWKRLVRDLDYFETGDKPYITQTTPHYHIEKGKIGLRFVPEGQHLWPSPEVGATRTGRSKYAQDKRFTAEAFLSVHELMPMMFYYFLLREKYSDEASAERVQGRIKRVIEDVYAVYDAFARGEIDTLDRLDACLADKGIRRGHLPRQMIAILSQEHKDMEEKVRKKLQEMMADTDHRLDMLDRQTDRKIRIGRKNAGLPKSGVIADWLVRDMMRFQPVAKDTSGKPLNNSKANSTEYRMLQRALALFGGEKERLTPYFRQMNLTGGNNPHPFLHETRWESHTNILSFYRSYLKARKAFLQSIGRSDRVENHRFLLLKEPKTDRQTLVAGWKGEFHLPRGIFTEAVRDCLIEMGYDEVGSYKEVGFMAKAVPLYFEWACKDRVQPFYDYPFNVGNSLKPKKGRFLSKEDRAEEWESGKERFRDLEAWSHSAARRIEDAFAGIEYASPGNKKKIEQLLQDLSLWETFESKLKVKADKINIAKLKKEILEAQEHPYLDFKSWQKFERELRLVKNQDIITWMMCRDLMEENKVEGLDTGTLYLKDIRTEVQEQGSLNVLNRVKPMRLPVVVYRADSRGHVHKEQAPLATVYIEERDTKLLKQGNFKSFVKDRRLNGLFSFVDTGGLAMEQYPISKLRVEYELAKYQTARVCVFEQTLELEESLLTRCPHLPDKNFRKMLESWSDPLLDKWPDLHGNVRLLIAVRNAFSHNQYPMYDEAVFSSIRKYDPSSLDAIEERMGLNIAHRLSEEVKQAKEMVERIIQV
>NZ_CP024593.1|WP_004584821.1|744466_745036_+|hypothetical-protein
MVFNFLIVSDEVEDFRREIAIDSEATFLDLQNAILDSVGYSHSELTSFFLCDEDWHKGQEITLMEMDTASDEDSYVMENTRLEEFIEDEHQRLVFEFDLMTERYFFIEVMDIVPGKSLSEPKLLTSEGLPPQQSSLDDLMDPTAIPTKQARGLDLEEDFFGDSEYNEDEIDREGFEGFDEITSDLSDNY
>NZ_CP024593.1|WP_021664579.1|745052_745955_+|tRNA-(adenosine(37)-N6)-dimethylallyltransferase-MiaA
METQDHTLYVLLGPTGVGKTDLSLDIAERLGSPIISADSRQIFRELPIGTAAPTPEQRARVPHLFVGTHSVRDYYSAGMYEVEVLEALKELFRKYRGVLLTGGSMMYIDAVCRGIDDIPDPFPEVREELYARYGAEGLDGILAQLRLLDPDYYAKVDRRNYKRVIHGLEICLSTGRPFSSFHRHEAKERPFRIVKIGLYREREELCRRIDARVLEMMEQGLEEEARAVYPLRHLNALNTVGYKEMFEYFDGSIDRAEAVRRIQRNSRVYARKQMTWFRRDSTIRWFHPEADKGTVLTLVT
>NZ_CP024593.1|WP_004584819.1|746079_747594_+|glycosyltransferase-family-39-protein
MKLSFQKKKAFSQTITSLIILVVLFLSCIPYFCKLDSLPIQLWDESRVSMNALCMYYNGDWGMTYYLDEPDMWNTKPPLLVWLQVIFMKLLGPGELAIRLPSALAAVATGILLFWTARKVYGNNLSGVIAAFILSTTPLFVNAHGMRTGDYDSLLLFWVSAFIFCSFFCSQAYRHERIKEAHRYLYIASLALSLAVLTKGVQALIVVPAVLAFVIFYGGPRRILKDKHLYFAFLLFVLIAGAWYLGREIKSAGYLQAIWENELGGRYFDSDSLLNRKSGYFYPTYLWEEYRWGTAIFGGCLLYAVLYGRKRSRVFALYLALCIVFYLSILSMSVTKIWWYMLPIVPPMTLIIAGIGVPVMYRLKKLYRPAVIAPVSLLLVVFFFAIPFAGIMKKIQTHESQDDLSNYLRRLTEIEDEKEIRTNPLILVYGEEYYQRAPLGFYVLQLQKRGIEVEYKKREELESGDFVCVAEQWAQEYVDARYRYEEVGREGKDIKFLRILGHRE
>NZ_CP024593.1|WP_004584818.1|747621_748581_+|glycosyltransferase-family-2-protein
MSINTSYTKDLSIVVPIYNEEKGIPELVRRLSAAAASITEDYELIFVNDGSRDGSMELLRSLCKGDDRFFYINLSRNFGHQIAVSAGLDHVRGKATVIIDGDLQDPPELIPELYAKYREGYEVVYAQRKHREGETWFKKATAKGFYRTMRKITSIDMPLDTGDFRLIDRKIVQCLREMPEQNKFLRGQIAWMGFRQTGVQFDRDERKYGQTNYPLRKMLALAIDGITGFSSRPLEWVAQLGAWVSLLSLFVIVYALISHFLLDKTVSGWTSVIVSSMFLGGVQLICLGVIGTYISKINKNIVARPLYLVAESNIAADER
>NZ_CP024593.1|WP_099811722.1|748591_749500_-|DMT-family-transporter
MTSSRLYGLAVGILSSATFGLIPLFTLPISAKGASFELILFYRFFFAAIAIGILHRLSGGSFKVSRADIGPLVLLGFLYAGTALFLFHGYGYMASGVATTIHFLYPLFVTALMLLFFGERLSPVPLTAIFIALIGVGLLMGLTGGGDRVGLTGFVIVAISALCYALYIVFVNRSRIRIMPGRRLTFYVFVAAAGFCLINVLVRQGEVAPLPDAASWGNILLLALVPTVISNLALVVAVRNIGSTLTSALGAMEPLTSVLVGVWVFDEVLGASAIVGMGCILIAVGLIVFSEPLELTLRRRRR
>NZ_CP024593.1|WP_099811723.1|749726_751691_-|transcription-termination-factor-Rho
MQKYTIVDLNEKAEAELAAIAGELGIANAGSMPKQELIYKILDEQAISVAGVRKEKQKTTEDRHTERRKPGRPRKNAEEEAPESEDAAAAPAEPNDEEAQAKRKRGRPRKAAEEIAEETREDVQQLVALAAAEETNATEKESAGRKPAAKTSTASPAKALPRPAETTPRVAPSPPPTTPVSEPAKDDAKPETPAPPPAIESITTTPAAGAVDEGGARRLVFRHKNSSSVLDQVLPYSSPQPPQRPKPAGAPVGSSPIRQRQAAGVPTPRREPQQLLYNFDGILECMGVLEIMPDGYGFLRSSDYNYLSSPDDVYVSQQQIKHNGLKTGDVVAGTIRPPREGEKYFPFVQLRSVNGRSPEEIRDRVPFDHLTPLFPEEKFTLEAPGIRAVNDKISVRVVDLFAPIGKGQRGLIVSQPKTGKTMLLKDIANAIAANHPEVYMIVLLIDERPEEVTDMARSVNAEVIASTFDEPAERHVKIAEIVLNKAKRMVECGHDVVILLDSITRLARAYNTVQPASGKVLSGGVDANALQKPKRFFGAARNIENGGSLTILATALTDTGSKMDEVIFEEFKGTGNMELQLDRRLSNKRIFPAVDIMSSSTRRDDLLQDETTLNRMWILRKYLSDMNPVEAMEFVRKQLENTHTNMEFLASMSN
>NZ_CP024593.1|WP_012458422.1|752366_752885_+|DUF4496-domain-containing-protein
MSLKYVIKKSVAKIGPKAGQTIYYAQPAAQDSVTFHSLCKRIAEESALTSADVKGILDRLVNILSEELPNGKTVRIGELGSFRLSFGSKQLDDPKNFSVDQIQKHRLVFIPSAELKSIPARGKLRPGSSALAFDYERVEPQPKKKPGTGDNQTPSPSTPGGGGGQGGTGGGL
>NZ_CP024593.1|WP_021664583.1|752917_753913_+|hypothetical-protein
MFRISRLGIVLLVSLIACNLSKAQNTTKDLINLSIKYLEQNDSTAFRKTYQDIFMQYVTEALCAPFDKAIQDRDQTYIQARLDSLTSDPEEDAFTYHLLSKPEYQVFYYTLPRWEVYKSWIDSVERNPHADMRNEIWQIQREDQGIRILWLRLPNETGDNIRKKVRDEILLVDRQNTERAIHIIDTFGEWPGANRLGCSADQTLWLCIQHADQRPEVATRYLPMLQKAVEEKRTDPMHYAYLVDRIRMHECKEQIYGTQTYHVKEENGNKFFFVIPIEDIDHVDERRAGIGMDPLSDYVNSMGYDWDIRQYKKDLPKIWKYYRHSCEKKKN

Crispr_ID: NZ_CP024593_4

• CRISPR_ID: NZ_CP024593_4
• CRISPR_location: 917337-917432
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: DEDDh

Consensus repeat of NZ_CP024593_4

Consensus_repeat	Method
CGTCAAGCTCCTAGACTCTACGACCATTAC	CRISPRCasFinder

spacers of NZ_CP024593_4

>4.1|917367|36|NZ_CP024593|CRISPRCasFinder
AACGTTTGCATGATGGAAAAATTGGTCGCCACCCTT

CRISPR arrays and Neighbor proteins around NZ_CP024593_4

CRISPR arrays

The CRISPR arrays of NZ_CP024593_4

>merge|NZ_CP024593|4|917337-917432|CRISPRCasFinder
CGTCAAGCTCCTAGACTCTACGACCATTACAACGTTTGCATGATGGAAAAATTGGTCGCCACCCTTCGTCAAGCTCCTAGACTCTACGACCATTAC

>NZ_CP024593|4|4|917337-917432|CRISPRCasFinder
CGTCAAGCTCCTAGACTCTACGACCATTAC	AACGTTTGCATGATGGAAAAATTGGTCGCCACCCTT
CGTCAAGCTCCTAGACTCTACGACCATTAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024593.1|WP_097633495.1|906685_908053_+|DUF4270-family-protein	unknown	unknown	gnl|CDD|379464
NZ_CP024593.1|WP_088477124.1|930993_932208_-|bifunctional-phosphopantothenoylcysteine-decarboxylase/phosphopantothenate--cysteine-ligase-CoaBC	unknown	unknown	gnl|CDD|235513
NZ_CP024593.1|WP_099810602.1|926229_926865_+|transposase	unknown	unknown	gnl|CDD|377531
NZ_CP024593.1|WP_004583517.1|932233_933013_-|3'-5'-exonuclease	DEDDh	cd06127_DEDDh_CAS-I	gnl|CDD|176648
NZ_CP024593.1|WP_099811767.1|908155_909391_+|nucleoside-permease	unknown	unknown	gnl|CDD|340866
NZ_CP024593.1|WP_099811766.1|903016_905140_-|RecQ-family-ATP-dependent-DNA-helicase	unknown	unknown	gnl|CDD|223588
NZ_CP024593.1|WP_099810601.1|928418_930074_-|DNA-repair-protein-RecN	unknown	unknown	gnl|CDD|223571
NZ_CP024593.1|WP_021679427.1|899192_899612_-|DUF1232-domain-containing-protein	unknown	unknown	gnl|CDD|225876
NZ_CP024593.1|WP_099811765.1|900853_902527_-|AMP-binding-protein	unknown	unknown	gnl|CDD|341240
NZ_CP024593.1|WP_099810606.1|919296_920316_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379240
NZ_CP024593.1|WP_004583452.1|905767_906583_+|glycogen/starch-synthase	unknown	unknown	gnl|CDD|377972
NZ_CP024593.1|WP_004583513.1|927672_928422_-|23S-rRNA-(guanosine(2251)-2'-O)-methyltransferase-RlmB	unknown	unknown	gnl|CDD|349976
NZ_CP024593.1|WP_077082808.1|918392_919316_+|DUF2156-domain-containing-protein	unknown	unknown	gnl|CDD|378310
NZ_CP024593.1|WP_099896717.1|920763_925962_+|DUF2436-domain-containing-protein	unknown	unknown	gnl|CDD|199211
NZ_CP024593.1|WP_077491272.1|905285_905429_-|DUF1661-domain-containing-protein	unknown	unknown	gnl|CDD|285160
NZ_CP024593.1|WP_004583512.1|927266_927647_-|RidA-family-protein	unknown	unknown	gnl|CDD|129116
NZ_CP024593.1|WP_099810599.1|930088_930997_-|DUF4835-family-protein	unknown	unknown	gnl|CDD|379771
NZ_CP024593.1|WP_099896716.1|909772_916267_+|DUF2436-domain-containing-protein	unknown	unknown	gnl|CDD|284979
NZ_CP024593.1|WP_004583457.1|899748_900252_+|RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|224511
NZ_CP024593.1|WP_004583456.1|900470_900683_-|hypothetical-protein	unknown	unknown	gnl|CDD|339724

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP024593.1|WP_004583517.1|932233_933013_-|3'-5'-exonuclease	DEDDh	cd06127_DEDDh_CAS-I	5.7e-39	128.5	0.1

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP024593.1|WP_097633495.1|906685_908053_+|DUF4270-family-protein	gnl|CDD|379464	pfam14092, DUF4270, Domain of unknown function (DUF4270). This family of lipoproteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 444 and 534 amino acids in length.	1.7425e-49
NZ_CP024593.1|WP_088477124.1|930993_932208_-|bifunctional-phosphopantothenoylcysteine-decarboxylase/phosphopantothenate--cysteine-ligase-CoaBC	gnl|CDD|235513	PRK05579, PRK05579, bifunctional phosphopantothenoylcysteine decarboxylase/phosphopantothenate synthase; Validated.	1.06202e-178
NZ_CP024593.1|WP_099810602.1|926229_926865_+|transposase	gnl|CDD|377531	pfam05598, DUF772, Transposase domain (DUF772). This presumed domain is found at the N-terminus of many proteins found in transposons.	3.38836e-22
NZ_CP024593.1|WP_004583517.1|932233_933013_-|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.	5.05446e-43
NZ_CP024593.1|WP_099811767.1|908155_909391_+|nucleoside-permease	gnl|CDD|340866	cd06177, MFS_NHS, Nucleoside:H(+) symporter family of the Major Facilitator Superfamily of transporters. The prototypical members of the Nucleoside:H(+) symporter (NHS) family are Escherichia coli nucleoside permease NupG and xanthosine permease. Nucleoside:H(+) symporters are proton-driven transporters that facilitate the import of nucleosides across the cytoplasmic membrane. NupG is a broad-specificity transporter of purine and pyrimidine nucleosides. Xanthosine permease is involved in the uptake of xanthosine and other nucleosides such as inosine, adenosine, cytidine, uridine and thymidine. The NHS family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	7.87934e-180
NZ_CP024593.1|WP_099811766.1|903016_905140_-|RecQ-family-ATP-dependent-DNA-helicase	gnl|CDD|223588	COG0514, RecQ, Superfamily II DNA helicase [DNA replication, recombination, and repair].	3.51716e-145
NZ_CP024593.1|WP_099810601.1|928418_930074_-|DNA-repair-protein-RecN	gnl|CDD|223571	COG0497, RecN, ATPase involved in DNA repair [DNA replication, recombination, and repair].	1.4833e-167
NZ_CP024593.1|WP_021679427.1|899192_899612_-|DUF1232-domain-containing-protein	gnl|CDD|225876	COG3339, COG3339, Uncharacterized conserved protein [Function unknown].	7.4651e-14
NZ_CP024593.1|WP_099811765.1|900853_902527_-|AMP-binding-protein	gnl|CDD|341240	cd05914, LC_FACL_like, Uncharacterized subfamily of fatty acid CoA ligase (FACL). The members of this family are bacterial long-chain fatty acid CoA synthetase, most of which are as yet uncharacterized. LC-FACS catalyzes the formation of fatty acyl-CoA in a two-step reaction: the formation of a fatty acyl-AMP molecule as an intermediate, and the formation of a fatty acyl-CoA. Free fatty acids must be "activated" to their CoA thioesters before participating in most catabolic and anabolic reactions.	1.40159e-148
NZ_CP024593.1|WP_099810606.1|919296_920316_+|GNAT-family-N-acetyltransferase	gnl|CDD|379240	pfam13527, Acetyltransf_9, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.19372e-25
NZ_CP024593.1|WP_004583452.1|905767_906583_+|glycogen/starch-synthase	gnl|CDD|377972	pfam08323, Glyco_transf_5, Starch synthase catalytic domain.	5.40303e-64
NZ_CP024593.1|WP_004583513.1|927672_928422_-|23S-rRNA-(guanosine(2251)-2'-O)-methyltransferase-RlmB	gnl|CDD|349976	cd18103, SpoU-like_RlmB, SAM-dependent rRNA methylase related to RlmB. 23S rRNA-M2G2251-MTase RlmB catalyzes the methylation of guanosine 2251, a modification conserved in the peptidyltransferase domain of 23S 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.	2.70839e-63
NZ_CP024593.1|WP_077082808.1|918392_919316_+|DUF2156-domain-containing-protein	gnl|CDD|378310	pfam09924, DUF2156, Uncharacterized conserved protein (DUF2156). This domain, found in various hypothetical prokaryotic proteins, has no known function.	4.76187e-55
NZ_CP024593.1|WP_099896717.1|920763_925962_+|DUF2436-domain-containing-protein	gnl|CDD|199211	cd10913, Peptidase_C25_N_gingipain, gingipain subgroup of the Peptidase C25 family N-terminal domain. Gingipain, produced by Porphyromonas gingivalis, exemplifies the Peptidase family C25, a unique class of cysteine proteases. P. gingivalis is one of the primary gram-negative pathogens that causes periodontitis, a disease also associated with other diseases such as diabetes and cardiovascular disease. The gingipain subgroup contains extracellular Arg- and Lys-specific proteinases called Arg-gingipain (Rgp) and Lys-gingipain (Kgp); RgpA and RgpB are homologous Arg-specific gingipains encoded by two closely related genes, rgpA and rgpB, while Lys-specific gingipain is encoded by the single kgp gene. Mutant studies have shown that, among the large quantities of proteolytic enzymes produced by P. gingivalis, these three proteases are major virulence factors of this bacterium. All three genes encode an N-terminal pre-pro fragment, followed by the protease domain; however, rgpA and kgp also encode additional C-terminal HA (hemaglutinin/adhesion) subunits which consist of several sequence-related adhesion domains. Although unique, their cysteine protease active site residues (His and Cys) forming the catalytic dyad, are well-conserved, cleaving the C-terminal peptide bond with Arg or Lys residues. Gingipains are evolutionarily related to other highly specific proteases including caspases, clostripain, legumains, and separase. Gingipains function by dysregulating host defense and inflammatory responses, and degrading host proteins, e.g. tissue, cells, matrix, plasma and immunological proteins. It has been suggested that they enhance gingival crevicular fluid (GCF) production through activation of the kallikrein/kinin pathways, thus increasing vascular permeability and causing gingival inflammation, a distinctive feature of periodontitis. RgpA and RgpB are also able to cleave and activate coagulation factors IX and X in order to activate prothrombin to produce thrombin, which in turn increases production of GCF. The gingipains also play a pivotal role in the survival of P. gingivalis in the host by attacking the host defense system through cleavage of several immunological molecules, while at the same time evading the host-immune response by dysregulating the cytokine network.	1.89597e-111
NZ_CP024593.1|WP_077491272.1|905285_905429_-|DUF1661-domain-containing-protein	gnl|CDD|285160	pfam07877, DUF1661, Protein of unknown function (DUF1661). This is a family containing bacterial proteins of unknown function. Many of the proteins in this family are hypothetical.	0.000114748
NZ_CP024593.1|WP_004583512.1|927266_927647_-|RidA-family-protein	gnl|CDD|129116	TIGR00004, RutC_family_protein, reactive intermediate/imine deaminase. This protein was described initially as an inhibitor of protein synthesis intiation, then as an endoribonuclease active on single-stranded mRNA, endoribonuclease L-PSP. Members of this family, conserved in all domains of life and often with several members per bacterial genome, appear to catalyze a reaction that minimizes toxic by-products from reactions catalyzed by pyridoxal phosphate-dependent enzymes. [Cellular processes, Other].	6.21131e-65
NZ_CP024593.1|WP_099810599.1|930088_930997_-|DUF4835-family-protein	gnl|CDD|379771	pfam16119, DUF4835, Domain of unknown function (DUF4835). This family consists of uncharacterized proteins of around 300 residues in length and is mainly found in bacteria from the Cytophaga-Flavobacteria-Bacteroides (CFB) group, both environmental and from human microbiome. The function of this family is unknown.	4.66691e-130
NZ_CP024593.1|WP_099896716.1|909772_916267_+|DUF2436-domain-containing-protein	gnl|CDD|284979	pfam07675, Cleaved_Adhesin, Cleaved Adhesin Domain. This is a family of bacterial protein modules thought to function in various roles including cell adhesion, cell lysis and carbohydrate binding. A tandem repeat of these modules (either two or three repeats) constitute the haemagglutinin/adhesin (HA) regions of the gingipains, RgpA, Kgp, and Lys-gingipain HG66 expressed by Porphyromonas gingivalis (Bacteroides gingivalis). They form components of the major extracellular virulence complex RgpA-Kgp - a mixture of proteinases and adhesin domains. The adhesin domains in this complex are found in proteinase-cleaved forms when isolated from the cell surface. Haemagglutinin genes of P. gingivalis (hagA1 HAGA1_PORGI - and hagA2 HAGA2_PORGI) suggest that such proteins are composed of eight to ten tandem repeats of these adhesin modules. Genomic data predicts that homologous protein modules are also expressed by a number of other bacteria and form part of putative multi-domain proteins. These domains may be acting in concert with other adhesion modules thought to be part of these multi-domain proteins such as fibronectin type III, pfam00041, and Meprin, A5, mu (MAM), pfam00629, domains.	7.52541e-79
NZ_CP024593.1|WP_004583457.1|899748_900252_+|RNA-polymerase-sigma-factor	gnl|CDD|224511	COG1595, RpoE, DNA-directed RNA polymerase specialized sigma subunit, sigma24 homolog [Transcription].	2.68352e-33
NZ_CP024593.1|WP_004583456.1|900470_900683_-|hypothetical-protein	gnl|CDD|339724	pfam16386, DUF4995, Domain of unknown function. This family around 100 residues locates in the N-terminal of some uncharacterized proteins and glucuronyl hydrolases in various Bacteroides species. The function of this family remains unknown.	0.000505396

Protein sequences

>NZ_CP024593.1|WP_099896716.1|909772_916267_+|DUF2436-domain-containing-protein
MRKLNSLFSLAVLLSLLCWGQTAAAQGGPKTAPSVTHQAVQKGIRTSKAKDLRDPIPAGMARIILEAHDVWEDGTGYQMLWDADHNQYGASIPEESFWFANGTIPAGLYDPFEYKVPVNADASFSPTNFVLDGTASADIPAGTYDYVIINPNPGIIYIVGEGVSKGNDYVVEAGKTYHFTVQRQGPGDAASVVVTGEGGNEFAPVQNLQWSVSGQTVTLTWQAPASDKRTYVLNESFDTQTLPNGWTMIDADGDGHNWLSTINVYNTATHTGDGAMFSKSWTASGGAKIDLSPDNYLVTPKFTVPENGKLSYWVSSQEPWTNEHYGVFLSTTGNEAANFTIKLLEETLGSGKPAPMNLVKSEGVKAPAPYQERTIDLSAYAGQQVYLAFRHFGCTGIFRLYLDDVAVSGEGSSNDYTYTVYRDNVVIAQNLTATTFNQENVAPGQYNYCVEVKYTAGVSPKVCKDVTVEGSNEFAPVQNLTGSAVGQKVTLKWDAPNGTPNPNPGTTTLSESFENGIPASWKTIDADGDGNNWTTTPPPGGTSFAGHNSAICVSSASYINFEGPQNPDNYLVTPELSLPNGGTLTFWVCAQDANYASEHYAVYASSTGNDASNFANALLEEVLTAKTVVTAPEAIRGTRVQGTWYQKTVQLPAGTKYVAFRHFGCTDFFWINLDEVEIKANGKRADFTETFESSTHGETPAEWTTIDADGDGQGWLCLSSGQLGWLTAHGGTNVVASFSWNGMALNPDNYLISKDVTGATKVKYYYAVNDGFPGDHYAVMISKTGTNAGDFTVVFEETPNGINKGGARFGLSTEANGAKPQSVWIERTVDLPAGTKYVAFRHYNCSDLNYILLDDIQFTMGGSPTPTDYTYTVYRDGTKIKEGLTETTFEEDGVATGNHEYCVEVKYTAGVSPKECVNVTVDPVQFNPVQNLTGSAVGQKVTLKWDAPNGTPNPNPGTTTLSESFENGIPASWKTIDADGDGNNWTTTPPPGGSSFAGHNSAICVSSASYINFEGPQNPDNYLVTPELSLPNGGTLTFWVCAQDANYASEHYAVYASSTGNDASNFANALLEEVLTAKTVVTAPEAIRGTRVQGTWYQKTVQLPAGTKYVAFRHFGCTDFFWINLDDVEIKANGKRADFTETFESSTHGETPAEWTTIDADGDGQGWLCLSSGQLGWLTAHGGTNVVASFSWNGMALNPDNYLISKDVTGATKVKYYYAVNDGFPGDHYAVMISKTGTNAGDFTVVFEETPNGINKGGARFGLSTEANGAKPQSVWIERTVDLPAGTKYVAFRHYNCSDLNYILLDDIQFTMGGSPTPTDYTYTVYRDGTKIKEGLTETTFEEDGVATGNHEYCVEVKYTAGVSPKECVNVTVDPVQFNPVQNLTGSAVGQKVTLKWDAPNGTPNPNPGTTTLSESFENGIPASWKTIDADGDGNNWTTTPPPGGSSFAGHNSAICVSSASYINFEGPQNPDNYLVTPELSLPNGGTLTFWVCAQDANYASEHYAVYASSTGNDASNFANALLEEVLTAKTVVTAPEAIRGTRVQGTWYQKTVQLPAGTKYVAFRHFGCTDFFWINLDDVEIKANGKRADFTETFESSTHGETPAEWTTIDADGDGQGWLCLSSGQLGWLTAHGGTNVVASFSWNGMALNPDNYLISKDVTGATKVKYYYAVNDGFPGDHYAVMISKTGTNAGDFTVVFEETPNGINKGGARFGLSTEADGAKPQSVWIERTVDLPAGTKYVAFRHYNCSDLNYILLDDIQFTMGGSPTPTDYTYTVYRDGTKIKEGLTETTFEEDGVATGNHEYCVEVKYTAGVSPKVCVNVTINPTQFNPVQNLTAEQAPNSMDAILKWNAPASKRAEVLNEDFENGIPASWKTIDADGDGNNWTTTPPPGGTSFAGHNSAICVSSASYINFEGPQNPDNYLVTPELSLPGGGTLTFWVCAQDANYASEHYAVYASSTGNDASNFANALLEEVLTAKTVVTAPEAIRGTRAQGTWYQKTVQLPAGTKYVAFRHFGCTDFFWINLDDVVITSGNAPSYTYTIYRNNTQIASGVTETTYRDPDLATGFYTYGVKVVYPNGESAIETATLNITSLADVTAQKPYTLTVVGKTITVTCQGEAMIYDMNGRRVAAGRNTVVYTAQGGHYAVMVVVDGKSYVEKLAVK
>NZ_CP024593.1|WP_099811767.1|908155_909391_+|nucleoside-permease
MMKQLKYRLILMNFLQFFIWGAWLISLGGYMASVLHYSGLEIGAIYGTMGIASLFMPGLLGILADKYVAAQKLLGACHLIGAILLVYASTLSSYSVFYPVMLLLCMSYMPTLALTNTIAYTAMEKAGMDIVREFPSIRVWGTVGFILAMWTVDICGWVMSSMQFYVSAVASLALGLYAFALPHCPPAKENKKKGMLAVLGLDAFVLFRQRRMAIFFLFAMLLGAALQVTNTFGNPFLSHFADTYSESFAVQHPNVLLSLSQISETLFILTIPFFMGRFGIKRVMLMSMLAWVLRFAFFGLGNPGSGFIFLVLSMIVYGMAFDFFNISGSMFVDRETTPSIRAAAQGLFMIMTNGIGAIIGGFASGWVVDRFTDAGHTAWSTVWYIFAAYALVIAILFAFFFKSESSPLSRS
>NZ_CP024593.1|WP_097633495.1|906685_908053_+|DUF4270-family-protein
MKRYLLLVFSLMALLAVACDDDLSPIGGSIQPPSDPVSARVDTLEFSVKTIPMGDIYNRTNYTLLGDLTDPEYGDLKADYIMQFKSPRNFKFKYPPKDGKIDSVKLSINYDSWAGDSTSIMKVSIYKINKAIPPSYYSTQELASLLDETQIIASQTFKAGNDSAFHRVRIPLPNEIGQKIYDLSVNNPSVFDTQESFYNNVLGGLYVTTTTGTGVVLSVYNTQMAIFYSYKVAADSTATASETFVNTSESYQVNHIKNSQISHLLQENDSLTCVKSPAGVMTQLTISKEQFTDAFTSNLSSSLAWQIGEAQFNISASKPSEGLMLSPPSYLLLLPQDSVRNFFEQEQTELMQPRTAFLSTIYNIKKREYRFSNISRLLMEHIKNNTEKTPEGKPYITKDLVLVLLPVKRQVAGASNSLYTSQLNNFMFPSGVKLQLGKKNKTARIGVYSMTYTDN
>NZ_CP024593.1|WP_004583452.1|905767_906583_+|glycogen/starch-synthase
MDSKKILYISQEIFPYLPETDISVVSRKLPQTIQERGNEVRIFMPRYGIINERRNQLHEVIRLSGINMIINDNDHPLIIKVASIQSARMQVYFIDNDDFFKRKTMYDIKPKQENDNDERAIFFVRGALEAIKKLRWIPDVIHCHGWFTALAALYLKKMYADDPCLQKAKVVYSVYDDAGQGVIPETLFGKLGFDKITADDLSVMEQSSDYLALNRLAIRYADGVIQGSETIAPELTDYISSLEGKAFLPYQGKEDYEEAFDNFYSDLLTTN
>NZ_CP024593.1|WP_077491272.1|905285_905429_-|DUF1661-domain-containing-protein
MRRVKVFLLVREKKNLRATTKKISRHFSQKHEPQSQLLWFRNCRRSA
>NZ_CP024593.1|WP_099811766.1|903016_905140_-|RecQ-family-ATP-dependent-DNA-helicase
MSEELQHLPPGERLYPLSTDMKELPDRYLHGEVYDHEQSDEIGGEEEGFFPPMPEEFSNEIEAPSLHTPEEVLLHYWGYPSFRPVQLPIIESVLAGKDTLGLLPTGGGKSITFQVPGLLLPGLTLVVTPLIALMRDQVMGLRQKGIKATAVHAGMTREQIITTLDNCIYGRYKFLYVSPERLGSELFLSRLHALRVSLLVVDECHCISQWGYDFRPAYLSIADIREALPDVPVLALTATATRPVIDDIQRILRFPEPNVLRKSFFRPNLSYSIRRTADKETMLLHILSRVDGSAVVYCRNRDKARDLARFLGENGFSADFYHAGLNHVTREIRQKSWMEGETRIIVCTNAFGMGIDKPDVRLVLHMEMPSSPEEYFQEAGRAGRDGERAYAVLLAGEDDIFNLKRRVSNEFPPREYIATVYNRICNYLQIGEGEGFERSFDFDIDAFCRNFRMFPTQVLAAIRILDVAGIWEYREEKTRSRLTIQVQRDELYRMRSEQASDSVLTALMRTYDGLFADYVSIVESELAEKTGLSVDQVYQQLLLLNKAGIVNYIPQKNLPRIYFLTRREDAELLQIPRAAYEDRRDRLKARIDQSLRYIEEENTCRSRMLLAYFGEEQSHNCKLCDVCLRRKDGELRHHEVDDLLHFLEQRLTEETPYVLIADICREVHHHPDVVLKAIRFVMKESWQYSTDGDTVFLTHKLPGGLNL
>NZ_CP024593.1|WP_099811765.1|900853_902527_-|AMP-binding-protein
MIEQNFIRLYQDSFREHWALPALTNYDTKESYTYGEMAADIARRHLLFERIGLKPGDKVALLGKDSAEWCMTFMSVITYGAIIVPVLPDFNAADAASIVTHSDAKYLFVSDKIWETMDPSQLLLLCGAVSIRDYTVFLDRTEGGLLSQEVEGLSRSFSERYPSGFTAEDIRYAEVSNDDLILLNYTSGTTGFSKGVMLRANNLAGNVTYVKDRDIMFRGETILCFLPLAHTYSCAFNFLTPLTIGVHVYILGKIPSPLTLIKAFADVRPSFVIMVPLIIEKLYHKAIAPKIKTPLIKFLLRLPVLRKVIHKSIRSKLIESFGGNFRQIIIGGAALNDEVAHFLYRIGFPLTVGYGMTECGPLISYEDHSLWLPGSCGKSLSIMGVRIDHSGQERHSDSGDVGEIQVRGENVCLGYYKNAELTAELFTPDGWMRTGDLGTIDSLGNIFIKGRSKTMLLGSNGQNIYPEEIESKINNLPYVLESIVTERDGRLIALIVPDRQAIEHKGISPDQAWAYIGRCRAELNGQVGAYEKITAFVRHDEEFEKTPKRSIKRFLYT
>NZ_CP024593.1|WP_004583456.1|900470_900683_-|hypothetical-protein
MKKFVAFAAVIAAVSFASCNSQAKTEEAADSTAMDSATLVEDAAPVVDTAAMQIDSAAMKAEEATEQAAQ
>NZ_CP024593.1|WP_004583457.1|899748_900252_+|RNA-polymerase-sigma-factor
MNSVQFREKLLSLQDNMRNFALTLTANRDDAEDLLQDTTLRVLHNEDKFVDNVNFKGWVLTVMRNIFINNYHKLVRSQTVIDPNSDPYNVPLLNEGGEDTPDGTMTIKEITAAIASLNETLKQPFSMYVSGYKYNEISETLGIPLGTVKSRIFLARQELQQQLKDMR
>NZ_CP024593.1|WP_021679427.1|899192_899612_-|DUF1232-domain-containing-protein
MKRNHLQKRRQPTRKGFVDKLPTTLADISYYASYYQENALVNKVLKCCRLIGRFGTGQVLTLYYMLQAGEITMKEKLLLAGALGYFLLPFDLIPDIALPLIGFTDDLAVTSIVLRILHRRITPAIREKARLRAATIFED
>NZ_CP024593.1|WP_077082808.1|918392_919316_+|DUF2156-domain-containing-protein
MNIKFKPVEPADRSAITTITFSSVARICDLAFSNLYCWSFVYGTSWAIVEDCLIIRFKPKSRSHPVYLFPVGADPEQVVAAAHRLKAEVVHEDYPLIFMGVTPDIHRCIEEHCSAEYYFIEDEAYCDYIYERESLATLSGKKLQAKRNHINKFVSLYPDYTYDPVKDSDAEECLMLAHLWLDSRGDQDGRELEVEMVERAFRHRQELGLSGGVLRVGGRVVAFCLGSPINADTFGVHIEKADAMVEGAFAMINREFARSIPDTFRYINREEDLGLPGLRQAKLSYRPAILLPKQTAILRRDHDRIQA
>NZ_CP024593.1|WP_099810606.1|919296_920316_+|GNAT-family-N-acetyltransferase
MTESKREASVRLWRICFEDPEPFIELYFHEVFREDYTLLQYSETGEAVAHLQMLPYQLRIFGTSFSAGYISGACTHPDHRGKGIMRTMMAEALSAMYDRGDICSFLIPAETWLYDFYSRSGGYAPAFGRKQFLYRPNSIPQKFPSGYACTIGQGDYSFLSAEEHTDIRLAVQHTLGQWQTALKDFSLAGGNVAMLQDSAGKTVSQACFVPRENSLDIKLLVGDAEATFILVDHLLRSLDCDHASILAHSGSAPYGMLRILRPIPILEAFAQYHPAEVHSFAYSDPLFSQHNGTYHISKGRIVFSNNVQPENSLLPHHTPDSLVKDLFSPFPSALFLMLD
>NZ_CP024593.1|WP_099896717.1|920763_925962_+|DUF2436-domain-containing-protein
MRKLLLLIAASLLGVGLYAQNAKIKLDAPTTRTTCTNNSFKQFDASFSFNEVELTKVETKGGTFASVSIPGAFPTGEVGSPEVPAVRKLIAVPVGATPVVRVKSFTEQVYSLNQYGSEKLIPHQPSMSKSDDPEKVPFVYNAAAYARKGFVGQELTQVEMLGTMRGVRIAALTINPVQYDVVANQLKVRNNIEIEVSFQGADEVATQRLYDASFSPYFETAYKQLFNRDVYTDHGDLYNTPVRMLVVAGAKFKEALKPWLTWKAQKGFYLDVHYTDEAEVGTTNASIKAFIHKKYNDGLAASAAPVFLALVGDTDVISGEKGKKTKKVTDLYYSAVDGDYFPEMYTFRMSASSPEELTNIIDKVLMYEKATMPDKSYLEKVLLIAGADYSWNSQVGQPTIKYGMQYYYNQEHGYTDVYNYLKAPYTGCYSHLNTGVSFANYTAHGSETAWADPLLTTSQLKALTNKDKYFLAIGNCCITAQFDYVQPCFGEVITRVKEKGAYAYIGSSPNSYWGEDYYWSVGANAVFGVQPTFEGTSMGSYDATFLEDSYNTVNSIMWAGNLAATHAGNIGNITHIGAHYYWEAYHVLGDGSVMPYRAMPKTNTYTLPASLPQNQASYSIQASAGSYVAISKDGVLYGTGVANASGVATVNMTKQITENGNYDVVITRSNYLPVIKQIQAGEPSPYQPVSNLTATTQGQKVTLKWDAPSAKKAEGSREVKRIGDGLFVTIEPANDVRANEAKVVLAADNVWGDNTGYQFLLDADHNTFGSVIPATGPLFTGTASSNLYSANFEYLIPANADPVVTTQNIIVTGQGEVVIPGGVYDYCITNPEPASGKMWIAGDGGNQPARYDDFTFEAGKKYTFTMRRAGMGDGTDMEVEDDSPASYTYTVYRDGTKIKEGLTATTFEEDGVAAGNHEYCVEVKYTAGVSPKVCKDVTVEGSNEFAPVQNLTGSSVGQKVTLKWDAPNGTPNPNPNPNPNPGTTLSESFENGIPASWKTIDADGDGHGWKPGNAPGIAGYNSNGCVYSESFGLGGIGVLTPDNYLITPALDLPNGGKLTFWVCAQDANYASEHYAVYASSTGNDASNFTNALLEETITAKGVRSPEAIRGRIQGTWRQKTVDLPAGTKYVAFRHFQSTDMFYIDLDEVEIKANGKRADFTETFESSTHGEAPAEWTTIDADGDGQGWLCLSSGQLDWLTAHGGTNVVASFSWNGMALNPDNYLISKDVTGATKVKYYYAVNDGFPGDHYAVMISKTGTNAGDFTVVFEETPNGINKGGARFGLSTEANGAKPQSVWIERTVDLPAGTKYVAFRHYNCSDLNYILLDDIQFTMGGSPTPTDYTYTVYRDGTKIKEGLTETTFEEDGVATGNHEYCVEVKYTAGVSPKVCVNVTINPTQFNPVQNLTAEQAPNSMDAILKWNAPASKRAEVLNEDFENGIPASWKTIDADGDGNNWTTTPPPGGTSFAGHNSAICVSSASYINFEGPQNPDNYLVTPELSLPGGGTLTFWVCAQDANYASEHYAVYASSTGNDASNFANALLEEVLTAKTVVTAPEAIRGTRAQGTWYQKTVQLPAGTKYVAFRHFGCTDFFWINLDDVVITSGNAPSYTYTIYRNNTQIASGVTETTYRDPDLATGFYTYGVKVVYPNGESAIETATLNITSLADVTAQKPYTLTVVGKTITVTCQGEAMIYDMNGRRVAAGRNTVVYTAQGGHYAVMVVVDGKSYVEKLAVK
>NZ_CP024593.1|WP_099810602.1|926229_926865_+|transposase
MAYQSKNTDEHVTFADALLSKRYRKAQNDFLNQVDTLIDGRPIRTLINKKYTKRQNAIGAPAYDVILLFKMLLPKTWYNLSDCALEERINDSITFSRFLGLKMEEVSPDHSTISRFRSALTELGLMDKLLAQFNKQLSRHHISVREGVLVDASLVEIRSTIERTFGSIRRWFHGGRCRYRGLAKTHTQNILESIAFNLYRTPGIIMSSSLG
>NZ_CP024593.1|WP_004583512.1|927266_927647_-|RidA-family-protein
MKKVINTKNAPAAIGPYSQAILMGNMLYASGQLGLDPTTGNFVPGGVTEQTEQVFKNIRAILEEAGLTIANVVKTTCFLADMSDFAAMNAVYEKQFTGDFPARSAVAVKTLPKNGLVEIEIIAIKD
>NZ_CP024593.1|WP_004583513.1|927672_928422_-|23S-rRNA-(guanosine(2251)-2'-O)-methyltransferase-RlmB
MKNDKMIFGLHSISEAFEAGKEIDKIFIRRGLKTEQTEAIIREAVERCVPVMHVPIEKLDRLTSKNHQGVVAILSAIEYTRLDQLMPMLYEEGKAPFLLLLDGITDVRNFGAIARTAECAGVDAIIIPERGSVSVGGDAIKTSAGALHRIPVCRVTSIPGAIRSLQEYGIRIVAASEKAADLYTDVPMKLPLGIVMGAEDVGPSPDTLRMADGIVAIPQMGAIGSLNVSVAAGIVIYEVVRQQRLQSSN
>NZ_CP024593.1|WP_099810601.1|928418_930074_-|DNA-repair-protein-RecN
MLASLHIANYVLIDRLDIDFAPHFSVITGETGAGKSILLGALGLLVGGRADTSAIAPGTDRCIVEGRFTGFVPEMKAVLDRYDLDFDPDECTIRREISSKGKSRAFVNDTPAPLTALRELADFLIDIHSQHKNLLLGDSLFQLNVLDAYSGKPDLYAHYSKAYRVYAERKQKLEDLRKAAAATASEYDYWQFRFEQLDKAGLESGEEARLQEEQAMLTHALDIKRELGHSYSLLSDDERGLLSGLNKVEDALATIESYYPDSASFRQRVRDVRIELADIASDLGRRSDDVSYEPERLNAVTDRLDEILSLLHRYNADNSDALIAIRDDLAERLSRISTDEEEISRLEQEVLAFYKEIEAQASLLTEERIRAASALETSLCESLRKLNMPHVRFVVDIRSTEYGPHGADKVVFLFSANKQMEPEPVSEIASGGEIARLMLCLKALIADKRSLPAIVFDEIDTGVSGEVADRMGEIMAHMGQGMQVLAITHLPQIAARGERHYFVYKDETGERARTFIRELTPEERIREIARMQSGNNLTDVALAAAKELLAR
>NZ_CP024593.1|WP_099810599.1|930088_930997_-|DUF4835-family-protein
MRRRLWWGLWICLFFYTASAVSQELNAKVTINSERLGSNANAETFKTLERQLSDLLNLTRWTTATFSFAERIDCTFSINLTEVKDESQYKAELFVTSRRPIYNSSYFSPQLIWRDQELNFEYNQFDPIEYNETDLQSNLVASVVFYAYFILAMDFDSFSPLGGNSARSMMRQIVARAQAKQDWRGWKAFESTKNRYALAEAMNDAELETLRRFWYDYHRRALDEMVGNPNRGRTTVLELLPQLEAVYKVRPMSPLLSIFAAVKLDEIVNILSKANASEKQDAYKVLNKVFPTEGNKLNPLKK
>NZ_CP024593.1|WP_088477124.1|930993_932208_-|bifunctional-phosphopantothenoylcysteine-decarboxylase/phosphopantothenate--cysteine-ligase-CoaBC
MKSSLAGKHIVLGVTGSIAAYKAAVLTRLLIKKEAEVQIVITPAGKEFITPITLSALTSKPVISEFFSGRDGTWNSHVDLGLWADAMLIAPATASTIGKMAHGIADNMLVTTYLSAKAPVFVAPAMDLDMFRHPSTQHNMEILRSYGNHIIEPGEGELASHLVGKGRMEEPECIVEILEAFFKENDCKPLLGKRALVTAGPTYEKLDPVRFLGNYSSGKMGFCIAERLAELGASVTLVTGPTAMQTTVEGIDRIDVESAVEMLEACRKPFEKADITVLSAAVADYRPAERAEKKMKRETKGDFDLRLTANPDIAATLGALKRAGQRLVGFALETDSGEQEAMRKMKAKHMDAIVLNSLSDAGAGFGVGTNKITIFDSEGRPSDYPLKSKVEVAEDIVDYIIGLG
>NZ_CP024593.1|WP_004583517.1|932233_933013_-|3'-5'-exonuclease
MKLNLKNPLIFFDLETTGVDLVRDRIVEISILKVMPDGSEECKTRRINPERPIPPESTAIHGIRDEDVKDCPPFRSVAKSLAQWIEGCDLAGFNSTRFDVPMLVEEFLRAGVDIDLRHRKLIDVQTIFHKMEPRTLEAATRFYCNRTLENAHSAEADTRATYDVFKAQLDRYEGTLENDMAFLADFSRQSRNVDFAGRLVYDDNDNVIINFGKYRGRKALDVLRTDSGYYGWIMDADFTLNTKQEFTRLRMSLNNPETK

Crispr_ID: NZ_CP024593_5

• CRISPR_ID: NZ_CP024593_5
• CRISPR_location: 1048083-1048421
• CRISPR_type: TypeIII
• Repeat_type: NA
• Spacer_info: 4 spacers
• Cas_protein_info: cas2,cas1,cmr6gr7,cmr5gr11,cmr4gr7,cmr3gr5,cas10,cmr1gr7

Consensus repeat of NZ_CP024593_5

Consensus_repeat	Method
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAG	PILER-CR
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAG	CRISPRCasFinder
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAGT	CRT

spacers of NZ_CP024593_5

>5.1|1048120|35|NZ_CP024593|PILER-CR,CRISPRCasFinder
TTATCATACTTGATGTGAGAGATTCTGGAGATTAT
>5.2|1048192|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
TAAGTCTGTGGATGATGATCTTATTGCCAGTGTAGA
>5.3|1048265|43|NZ_CP024593|PILER-CR,CRISPRCasFinder
CCAAAACTGCTAAGGCTGCAGCTCAGAATGCACTAGACCAGTT
>5.4|1048345|39|NZ_CP024593|PILER-CR,CRISPRCasFinder
TATAGTTCAAGCTTCTGATACAGACTTGATTGAAGAAGA
>5.5|1048121|34|NZ_CP024593|CRT
TATCATACTTGATGTGAGAGATTCTGGAGATTAT
>5.6|1048193|35|NZ_CP024593|CRT
AAGTCTGTGGATGATGATCTTATTGCCAGTGTAGA
>5.7|1048266|42|NZ_CP024593|CRT
CAAAACTGCTAAGGCTGCAGCTCAGAATGCACTAGACCAGTT
>5.8|1048346|38|NZ_CP024593|CRT
ATAGTTCAAGCTTCTGATACAGACTTGATTGAAGAAGA

CRISPR arrays and Neighbor proteins around NZ_CP024593_5

CRISPR arrays

The CRISPR arrays of NZ_CP024593_5

>merge|NZ_CP024593|5|1048083-1048421|PILER-CR,CRISPRCasFinder,CRT
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAGTTATCATACTTGATGTGAGAGATTCTGGAGATTATGTCTTAATAGCCTTACAGACTGTGTATGTATAGTGAGTAAGTCTGTGGATGATGATCTTATTGCCAGTGTAGAGTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAGCCAAAACTGCTAAGGCTGCAGCTCAGAATGCACTAGACCAGTTGTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAGTATAGTTCAAGCTTCTGATACAGACTTGATTGAAGAAGAGTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAGT

>NZ_CP024593|5|2|1048083-1048420|PILER-CR
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAG	TTATCATACTTGATGTGAGAGATTCTGGAGATTAT
GTCTTAATAGCCTTACAGACTGTGTATGTATAGTGAG	TAAGTCTGTGGATGATGATCTTATTGCCAGTGTAGA
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAG	CCAAAACTGCTAAGGCTGCAGCTCAGAATGCACTAGACCAGTT
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAG	TATAGTTCAAGCTTCTGATACAGACTTGATTGAAGAAGA
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAG

>NZ_CP024593|5|5|1048083-1048420|CRISPRCasFinder
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAG	TTATCATACTTGATGTGAGAGATTCTGGAGATTAT
GTCTTAATAGCCTTACAGACTGTGTATGTATAGTGAG	TAAGTCTGTGGATGATGATCTTATTGCCAGTGTAGA
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAG	CCAAAACTGCTAAGGCTGCAGCTCAGAATGCACTAGACCAGTT
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAG	TATAGTTCAAGCTTCTGATACAGACTTGATTGAAGAAGA
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAG

>NZ_CP024593|5|2|1048083-1048421|CRT
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAGT	TATCATACTTGATGTGAGAGATTCTGGAGATTAT
GTCTTAATAGCCTTACAGACTGTGTATGTATAGTGAGT	AAGTCTGTGGATGATGATCTTATTGCCAGTGTAGA
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAGC	CAAAACTGCTAAGGCTGCAGCTCAGAATGCACTAGACCAGTT
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAGT	ATAGTTCAAGCTTCTGATACAGACTTGATTGAAGAAGA
GTCTTAATAGCCTTACGGACTGTGTATGTATAGTGAGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024593.1|WP_099811797.1|1052283_1053057_-|type-III-B-CRISPR-module-RAMP-protein-Cmr6	cmr6gr7	cd09661_cmr6gr7_CAS-III-B	gnl|CDD|187792
NZ_CP024593.1|WP_099811794.1|1054226_1055444_-|type-III-B-CRISPR-module-associated-protein-Cmr3	cmr3gr5	cd09656_cmr3gr5_CAS-III-B	gnl|CDD|273855
NZ_CP024593.1|WP_099896724.1|1044503_1046507_-|hypothetical-protein	unknown	unknown	gnl|CDD|378965
NZ_CP024593.1|WP_099896725.1|1046536_1047127_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_099811795.1|1053487_1054213_-|type-III-B-CRISPR-module-RAMP-protein-Cmr4	cmr4gr7	cd09682_cmr4gr7_CAS-III-B	gnl|CDD|187813
NZ_CP024593.1|WP_157763372.1|1041730_1042279_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_099811793.1|1055445_1057149_-|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	cas10	cls000742_cas10_CAS-III	gnl|CDD|274208
NZ_CP024593.1|WP_099811796.1|1053053_1053491_-|type-III-B-CRISPR-module-associated-protein-Cmr5	cmr5gr11	mkCas0098_cmr5gr11_CAS-III-B	unknown
NZ_CP024593.1|WP_012458620.1|1058410_1058647_-|hypothetical-protein	cmr1gr7	mkCas0102_cmr1gr7_CAS-III-B	unknown
NZ_CP024593.1|WP_004585727.1|1042330_1042876_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_043894430.1|1039050_1039953_-|T9SS-type-A-sorting-domain-containing-protein	unknown	unknown	gnl|CDD|275036
NZ_CP024593.1|WP_005874926.1|1048822_1049113_-|CRISPR-associated-endonuclease-Cas2	cas2	pfam09827_cas2_CAS-I:CAS-II:CAS-III	gnl|CDD|187856
NZ_CP024593.1|WP_097555163.1|1057123_1058395_-|hypothetical-protein	cmr1gr7	mkCas0086_cmr1gr7_CAS-III-B	unknown
NZ_CP024593.1|WP_099896720.1|1040558_1041614_+|hemagglutinin	unknown	unknown	unknown
NZ_CP024593.1|WP_099811799.1|1047574_1047745_-|DUF1661-domain-containing-protein	unknown	unknown	gnl|CDD|285160
NZ_CP024593.1|WP_157763373.1|1042863_1043928_-|peptidoglycan-DD-metalloendopeptidase-family-protein	unknown	unknown	gnl|CDD|366703
NZ_CP024593.1|WP_077085190.1|1038067_1038955_+|tetratricopeptide-repeat-protein	unknown	unknown	gnl|CDD|276809
NZ_CP024593.1|WP_099896723.1|1043911_1044346_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_099811798.1|1049132_1052228_-|CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl|CDD|187766
NZ_CP024593.1|WP_012458621.1|1058648_1060232_-|hypothetical-protein	unknown	unknown	unknown

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP024593.1|WP_099811797.1|1052283_1053057_-|type-III-B-CRISPR-module-RAMP-protein-Cmr6	cmr6gr7	cd09661_cmr6gr7_CAS-III-B	4.3e-63	207.6	0.2
NZ_CP024593.1|WP_099811794.1|1054226_1055444_-|type-III-B-CRISPR-module-associated-protein-Cmr3	cmr3gr5	cd09656_cmr3gr5_CAS-III-B	3e-79	261.4	4.2
NZ_CP024593.1|WP_005874926.1|1048822_1049113_-|CRISPR-associated-endonuclease-Cas2	cas2	pfam09827_cas2_CAS-I:CAS-II:CAS-III	8.1e-20	65.7	0.2
NZ_CP024593.1|WP_097555163.1|1057123_1058395_-|hypothetical-protein	cmr1gr7	mkCas0086_cmr1gr7_CAS-III-B	1.3e-84	279.4	27.8
NZ_CP024593.1|WP_099811795.1|1053487_1054213_-|type-III-B-CRISPR-module-RAMP-protein-Cmr4	cmr4gr7	cd09682_cmr4gr7_CAS-III-B	2.4e-62	205.8	0.0
NZ_CP024593.1|WP_099811798.1|1049132_1052228_-|CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	2.1e-64	212.3	0.3
NZ_CP024593.1|WP_099811793.1|1055445_1057149_-|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	cas10	cls000742_cas10_CAS-III	1.9e-90	298.7	28.8
NZ_CP024593.1|WP_099811796.1|1053053_1053491_-|type-III-B-CRISPR-module-associated-protein-Cmr5	cmr5gr11	mkCas0098_cmr5gr11_CAS-III-B	5.1e-69	225.6	0.7
NZ_CP024593.1|WP_012458620.1|1058410_1058647_-|hypothetical-protein	cmr1gr7	mkCas0102_cmr1gr7_CAS-III-B	1.2e-47	154.9	5.3

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP024593.1|WP_099811797.1|1052283_1053057_-|type-III-B-CRISPR-module-RAMP-protein-Cmr6	gnl|CDD|187792	cd09661, Cmr6_III-B, CRISPR/Cas system-associated RAMP superfamily protein Cmr6. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; RAMP superfamily protein; This protein is a subunit of Cmr complex.	1.38731e-68
NZ_CP024593.1|WP_043894430.1|1039050_1039953_-|T9SS-type-A-sorting-domain-containing-protein	gnl|CDD|275036	TIGR04183, hypothetical_protein, Por secretion system C-terminal sorting domain. Species that include Porphyromonas gingivalis, Fibrobacter succinogenes, Flavobacterium johnsoniae, Cytophaga hutchinsonii, Gramella forsetii, Prevotella intermedia, and Salinibacter ruber average twenty or more copies of a C-terminal domain, represented by this model, associated with sorting to the outer membrane and covalent modification.	1.05077e-09
NZ_CP024593.1|WP_005874926.1|1048822_1049113_-|CRISPR-associated-endonuclease-Cas2	gnl|CDD|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	8.2336e-16
NZ_CP024593.1|WP_099811795.1|1053487_1054213_-|type-III-B-CRISPR-module-RAMP-protein-Cmr4	gnl|CDD|187813	cd09682, Cmr4_III-B, CRISPR/Cas system-associated RAMP superfamily protein Cmr4. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; RAMP superfamily protein; This protein is a subunit of Cmr complex.	1.50998e-75
NZ_CP024593.1|WP_099811799.1|1047574_1047745_-|DUF1661-domain-containing-protein	gnl|CDD|285160	pfam07877, DUF1661, Protein of unknown function (DUF1661). This is a family containing bacterial proteins of unknown function. Many of the proteins in this family are hypothetical.	3.3415e-08
NZ_CP024593.1|WP_157763373.1|1042863_1043928_-|peptidoglycan-DD-metalloendopeptidase-family-protein	gnl|CDD|366703	pfam01551, Peptidase_M23, Peptidase family M23. Members of this family are zinc metallopeptidases with a range of specificities. The peptidase family M23 is included in this family, these are Gly-Gly endopeptidases. Peptidase family M23 are also endopeptidases. This family also includes some bacterial lipoproteins for which no proteolytic activity has been demonstrated. This family also includes leukocyte cell-derived chemotaxin 2 (LECT2) proteins. LECT2 is a liver-specific protein which is thought to be linked to hepatocyte growth although the exact function of this protein is unknown.	9.32953e-17
NZ_CP024593.1|WP_077085190.1|1038067_1038955_+|tetratricopeptide-repeat-protein	gnl|CDD|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	3.96422e-14
NZ_CP024593.1|WP_099896724.1|1044503_1046507_-|hypothetical-protein	gnl|CDD|378965	pfam12836, HHH_3, Helix-hairpin-helix motif. The HhH domain is a short DNA-binding domain.	0.000734259
NZ_CP024593.1|WP_099811793.1|1055445_1057149_-|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	gnl|CDD|274208	TIGR02577, thermophile-specific_DNA_repair_system, CRISPR-associated protein Cas10/Cmr2, subtype III-B. This model represent a Crm2 family of the CRISPR-associated RAMP module, a set of six genes recurring found together in prokaryotic genomes. This gene cluster is found only in species with CRISPR repeats, usually near the repeats themselves. Because most of the six (but not this family) contain RAMP domains, and because its appearance in a genome appears to depend on other CRISPR-associated Cas genes, the set is designated the CRISPR RAMP module. This protein, typified by TM1794 from Thermotoga maritima, is designated Crm2, for CRISPR RAMP Module protein 2.	5.28589e-76
NZ_CP024593.1|WP_099811798.1|1049132_1052228_-|CRISPR-associated-endonuclease-Cas1	gnl|CDD|187766	cd09634, Cas1_I-II-III, CRISPR/Cas system-associated protein Cas1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas1 is the most universal CRISPR system protein thought to be involved in spacer integration; Cas1 is metal-dependent deoxyribonuclease, also binds RNA; Shown to possess a unique fold consisting of a N-terminal beta-strand domain and a C-terminal alpha-helical domain.	2.33587e-68
NZ_CP024593.1|WP_099811794.1|1054226_1055444_-|type-III-B-CRISPR-module-associated-protein-Cmr3	gnl|CDD|273855	TIGR01888, Hypothetical_protein_SSO1730, CRISPR type III-B/RAMP module-associated protein Cmr3. CRISPR is a term for Clustered Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR associated) proteins. This highly divergent family is found in at least ten different archaeal and bacterial species as part of the CRISPR RAMP modulue but is not a member of the RAMP superfamily itself. A typical example is TM1793 from Thermotoga maritima.	2.84631e-71

Protein sequences

>NZ_CP024593.1|WP_099811799.1|1047574_1047745_-|DUF1661-domain-containing-protein
MVREVKNYRATAKKFSRRFSRKHAPQSEHFRSVNFGEADLSEKESSVVFGGGDRLV
>NZ_CP024593.1|WP_099896725.1|1046536_1047127_-|hypothetical-protein
MKRTLVFLFLAAVLALRAEAQSAPEQSETKDFIFSPQKEMVYVAIGYPAGIGLPSLDNYNVEGASASFTVGYERGVKQLAEGLLLSIYAELDWAAFRSVSDKRSLPFSDDSAQDRFRFLAGAGVHKRLNPNIELYARGAVGASFFPENNGSSSRELKGGFNVSLRVGLSCSLRDNFAVFIDTGTSDIVRGGLALMW
>NZ_CP024593.1|WP_099896724.1|1044503_1046507_-|hypothetical-protein
MKPLLTVVCAILLSLPLGGQTVVPEWDEYIAEQIESGAIGEDEGAEFLERWMVQKQHPLDINTLTREDLEQFPFLNEFQIRRFLLYRHAHPEGFDSIWVLNEIAGWDRRTCLLLWPMLTVQKRSEPAAASFREILSYARHDVSVHTDAILQRQEGYRLDSRHPYRGDPWGGGLRWSYAMGNRFSLGLTASKDRGEPAFDKRRKGFDSYSAHFFMQGKGAVRAVALGDYRIGMGYGLLVNQASFMGMAYAYPRGGTTLRRAFTYAEDNFMRGAATALAQGRWALTAFYSRKGIDATVTEDGAIKAIYHTGLHRTDAEIARRNAATMTTAGTSVSYTDDRLRLTFNLLHLHWDGLRLLRAVGTQGIASLTDLERFSLVSADYSYLFGQGGTELFGEFAGAANGAVGTINGLRYTHPVGGSYMLVGRYIPADYWSYYRGAFARHSRPGNEWGVMGRAAWELPSDRTVRAFADYYGSFVPRFGRKEKTEALYWMFEGEKRLSALSWSCRIRGPADKRYRRSLAVRLRGRYMFDERWRLMASLQWSRSNSFDRELQTWQAPTGGKSFALRADYSGGKLLRVCSMDAVAFDTDSFADRLYEAVHNPRHHYSSAFFYGRGVRLGVFVRIAPLPHVEVESRIDHLLRRDTDTIGSAGELIRGQARTHLLMTVRYR
>NZ_CP024593.1|WP_099896723.1|1043911_1044346_-|hypothetical-protein
MRKVRFKARWALSVFFATVLISISCVKNDPQTTIEEPMLGTKPFSSDLARSLQKSFERDYQETRVRSISDADTTLYFEGLSPKWEFAVRGYSPTKNKEYLEVPIDAEIALLTEGIHSDPSLLEGDEVELQLYLLSHRKVIVNRF
>NZ_CP024593.1|WP_157763373.1|1042863_1043928_-|peptidoglycan-DD-metalloendopeptidase-family-protein
MSTGSERSYFISYIPSKRFIEEGRSFVHRPGFVPNQFDGVVQYHELNGDYINGYVFEDGLATKIIKRASAGESQENGSRDYDCVPQYVAEWYSWTGLEYDWEYHGWVFTTYRRKGIRFVGYECNYIQTPFQTEQSIAPDPGGGGGGSNVEPPEEEPKPCESKDGKRSNPLVVMALAPTSGDRYSAGRYGYTRSNGKKMHNGIDLYAEVGTPVYAMMDGIVTRVVDCQPNRSLSYGTASGLPIEYEKSGKDKNDAGNRITIRSTYNNDTIEHSYWHLQAETPIAINPSTQKTYKVGDKVLKGTIIGYTGITGNAYSVPNPHLHLNIRKNGKSHNPEDYLEATVKNQSKIDTPCDE
>NZ_CP024593.1|WP_004585727.1|1042330_1042876_-|hypothetical-protein
MRRIRIATVELLMFMAVAINIMAQNIGGVQIDVVPFTVKGFRIGETYSEAMQRRQLKGATIRETDTEFGVDRAFLFEEDESGKNYSYFNFSNDELREFLIQSNRFFLNMGKVQLGLGSSFDKLKDVPQLTLEQAMMGYGANRKPRKGVWVLRHPSLPEDFYYITIYVENEKITAIHGSLVP
>NZ_CP024593.1|WP_157763372.1|1041730_1042279_-|hypothetical-protein
MRRMKYSKIFFLLMLFFTVSSSYAQLGGSTVPLKTVFSVNGFQLGEVYPEAVQKSRFQGARMNENETEFGIDRVFIYGSEEENNYTYFLFNADELQEFFITDKVFSLDIGRVKIKVGEPLDKLKDVPELKMEQAIDYTAKPKPQPIKGGWVLRYPDLLEDAYRITVYEENGIVTALTGIVLP
>NZ_CP024593.1|WP_099896720.1|1040558_1041614_+|hemagglutinin
MTVENLRLQRLQNLEHYRFAKNVLTLCRTANIAKLNPKLPELEKAIEMEDLALNPPVANELTPQVIALDEERDRAYQALMSRVRSYAFDEDSQLRNAAARIEDVAARYGNVIRMNYDKETAAIENFLTDLKGENIRPLVTKLGVTALVDRLEKANKAFADFFLRRLSTDQRGKYDVKALRAETDRTLVAVVRRMDSIDDMEPSPEIRALIELYNRLVANRRALLARRASYGEAAVEKRRAEIAEMLRPLLARIVEEKKTAVFAGRTLGTGKNRHYLITFVAENGDEEDRWYRIDGERLVYVPEDELPKPKKKKKPASSTDTPSEPPVLPNPSQEGGSSSGGGEQGSTGGGL
>NZ_CP024593.1|WP_043894430.1|1039050_1039953_-|T9SS-type-A-sorting-domain-containing-protein
MAFAQVPKGNDKSKDEHILTWALPEELVIDNNSIVATYNSFLTPFNGMTMACASFFDVQDLLPYVGYTINRIDFHPTADEKNYEQVAASKFYICIWGNKEQTEVLYEQALPTIHKEDLSFGYGVDGEEDYYDEPMYLAELETPFVIPAGKALYIGCRVETQEGHAVGFGLDDGPAMKGKGDLVGSYLPGAAPMPFVPLSDIPARSMDANFYIYSRISLGSGTQDVLQHRMKVYPNPATTELHVEALSAWVGEQAAVYDMRGRRVSARTVDSEKLCIDIASLPVGVYMLRIGSYSAKFEKR
>NZ_CP024593.1|WP_077085190.1|1038067_1038955_+|tetratricopeptide-repeat-protein
MTDRFLHILRLSALCLLFSALLPPLFGQPTTARQDSLPADYTRLIDRSFEALGQGNLELAEQALRQAIKAYPDLPSGYALMNNLGAIQQRQGKPEEALLTYSAALQKLPDDKLLRMNRAMLLTEMGRTDEAIFDYNELLRAEPDNEIFHYGRAMLYLAKGMYGDAESDLEEILRINDSSLKARLGIALVATMKGEYDKAERLYNYVIDKLPKNAAAYEGRARLFLNKGMKGYALRDINKAFEYATPPAASLFVLRGEINAAIGDKKAAAEDYAAAESRGYSKESLDLLRAALRKQ
>NZ_CP024593.1|WP_005874926.1|1048822_1049113_-|CRISPR-associated-endonuclease-Cas2
MNDKKLLVAYDISSNRRRRKVARILEQCGIRINKSVFICSLRELTMDKLVEAVTSQTAKRDKVFFLPLCQHCYTAAWMSGHPTLPKSRRKRKSIVV
>NZ_CP024593.1|WP_099811798.1|1049132_1052228_-|CRISPR-associated-endonuclease-Cas1
MPLSTDSLPIFLSDFTAYHFSVRFRAERAIAFERKWYFMPRFALGNALKNSEQYAYLYGQIFKPQEEDTDESKGSGNTSRLIIRADKPSRKSLEAGEAMDLYITVVTRDPLLVGDFLSFLPEWQAYNFFRENDLTYDSYRLYNPTTQKYESGLRVEDAALTVDFFSRQAIRWGEILSVRFLSPASIKVDQILSAEIPYSRLMNRLSRRLYELYTQYLSRGETSVERYIFPDHDGLIYSQISMPRKATIKENRQYDMSGILGQLFYRVPYDPVAALMLSMAHWVHIGNHTIVGNGQIESTPGNDTLYRKWLSSLAADRDLPMAEAERQDLLEALRICSYIPQPYHSVNIPKGDGSYRQLHIPSAVDLHLQRSLAGILYPITESLSIAQSYAYRKGKGAVAAVRRVQHLLDSLDENHTVVRCDIDNFFDSIPVPSLLQKVQRTTEDPLLTRMLSLWMKSGTVDRKQQYARASSGIPQGSPLAPLLSNLYLEDTDRYIAGHITTEFIRYADDLLLFLPEKVDPLKALQDLSEHLKYRKGLKLNRDFVVSSIKSSFSFLGITFCADGSRSMSRDKKEGLKRKITLALHRDTENFSALSETIHGMEQYYRKLLEKVDIEAIDKVAATVYATYIASLPTSEARKSAKDNLLRLGFLSSETAKQTLREAMRQTVVSSADNFPIKKESEILREQQKRQLQEREEIFDLVVTEPGAFIGISRNHVLVRKYGKTICKQPAAQIEQISIISDGVSLSSNVTKYCRKKNIRVIFYNATGQAYASLNGMNTILPSVMEAQMRLSEEKKREFVLALIKNKVRNQGKLLRYYHKYYRHDKELKEPLSNAIAELKQLEGIPIAEGSSLADFRQHAMLHEARCAQVYWRAFALLVHRSGHEFEGREHKGAEGLVNQMLNYGYAILRSYVMKTIDLWQLNPNIGILHSTQDNKPALCFDLMEQYRAFVVDRSILALLAKGEDVGQNNKGLLDMPTRSRIISKINERWFATEYYRSGEKLFSDIMKLQTKDVRAFCCGKVKRIKFYTPKW
>NZ_CP024593.1|WP_099811797.1|1052283_1053057_-|type-III-B-CRISPR-module-RAMP-protein-Cmr6
MNFGYWYYREYFDTIKLNSEGIVTNFSTFNKGKNDKLIKGATLPPYDKENDIKDVTGFELKTCYPGLLCGVGYHHEINKPADEKGKKGKKVEEDKEDDPEVYNLGMYFDYTSGLPVIPGSSIKGMLRSAIEEWDFLADYELNNGVTREEIIEKVFVGKEYSIYDRDIFLDAIPIRVDNTLFGEDYITHHPNPLQNPNPVRFLRVEPGVTYQFRFILKDHGEKLTVDFKTKLFKAIICTFGLGAKTNVGYGQFVEPEK
>NZ_CP024593.1|WP_099811796.1|1053053_1053491_-|type-III-B-CRISPR-module-associated-protein-Cmr5
MNKKTIQDLIPKAMQAIEGVGIVGKDKKFKKVHEGYINALGPNIIQSGLLPTLIFYNKDERALWLRALYYMAVGEEDEMTDESSTVIIRLIIGKEGGRIENLKPKAKEWERKILEYAVALKLALRTFVAKESETGNTEQQKGGAQ
>NZ_CP024593.1|WP_099811795.1|1053487_1054213_-|type-III-B-CRISPR-module-RAMP-protein-Cmr4
MKTAAYMIHCLTNMHVGKGDATYEVVDKCVQRDVTTGMPCIYSSSLKGALRQFFSKQGFADIKYVFGSDVSRDVKDESKGNESDNSNEENPKEHSVGNFTFFQANLLAYPVQTTQEGATYILKTNKALQESIKEFAKLLSAPSNIEDLLPEGIEKDLSNEALEQLPVIARNQLDNGKSENLWYEEVVPAESRFVFFVSYDDEEIFAKFDKIIQEKVFQIGANGSIGYGFCKIANVTNPFKK
>NZ_CP024593.1|WP_099811794.1|1054226_1055444_-|type-III-B-CRISPR-module-associated-protein-Cmr3
MYTYLIKLTPLDKFFFGQKKTFGDDNANYFVYSSHFPQQTTLLGLLRYQLLQIAGEEVFKDNKIQDEHKAGELIGKQSFSPFVKDKLQFGIIQSLSPVFIIDKKKDEGKEEYFLPVGKRFQKKKEKAPYSLLHLSCEDECPPIFESRESQKEKEEAYDPKKGLASCWLSSKSHTLLNEEDFFTKDERIGIRKDYEGATNDDAFFCQRYYRFKNFKKVVEDEEAKVCKQPPVRVHDFCFATVLETEKAIEHEKLNGRIVYLGGERQPFLMEVSKEEKASDLTIGSSTLTGDENHYTVVLLSDAMIEPDHLRKVKFASTEVKDFACLLTHVGTQKFYNKENKRQEQYLKKSATALSLQKELYARGSVFYFDTKEQANQFCEDLEKVPNFHTIGYNHAIIIEPTKTKE
>NZ_CP024593.1|WP_099811793.1|1055445_1057149_-|type-III-B-CRISPR-associated-protein-Cas10/Cmr2
MNSKEVKNNAYTAITIGPIGKTLAKARSVKSFWTASYLFSWIMRELLKKLPEENFEVLSPHRAGKDVSEETSKKVGLFPDRLFAKGELEEKEFKRIKREIFGELAEKFKNAFQDEKDDIARKIDTERDPKRKRELEEIKSRYSNATSKSEDIRKYLENYLSISSITVELSSDCSILEQLNKYLDTQELFNKASSHTDEDYMELFIEASKNSFLEDYSKENTSSSGSNKDLKESSTKKRAFPSTSEIAVSGWEQNPPKDANGEVDYSKLTSKTGFRNCYKYLAVIKADGDGFGTYIKELKVDEEKEIKENGEKENELTRFTKSFFEFSVEVANELIQKTKAIPVYIGGDDLFLFAPVLEGNVEKDVFNLIKEIDDLFIQKEIGEGLSMSYGVSIFYYKSPMSEAIDIADSMLRKAKEEKEEKEKKKDTVAISIQKHSGQKIEFLLPCKHSSADETDRKESLYGKTVELVRAFKDDGNMLNSLIYWIEEMYEILFIEEVTQSQERINAVFDNFFDEEIHKENEVFFDLLKKFIHSMHHSEDTPRKLKDKKKLLHGILRYCQFVTAKKEK
>NZ_CP024593.1|WP_097555163.1|1057123_1058395_-|hypothetical-protein
MYKLEFELEQHTPIIHFQARDAGATLRASEVKPKLDKFILKEYKEKLPKSVIKEREEDKEKKEDKEVRKSLDYKMRIIARNVDSEDIDAKSAPMYFGNIKAIKPKRLVTAKSVQIIILVKNEVLKDCIEESIVRFFQLHNFGTRQSKGYGSFTIKVDGKKKIRDVYKYSFDVSGSDYKEVMNRINYFYKSLRSGINEYRGKGEKKRSILYFKSALHYYVTTVLEEQWDKKSIKEYFFPQQLEEEKTKHKVEDISSKEKNDFRDLLGFSTDEAWGKEYQIKKTCKKETDKGEEEFSRLKSPIQFKPIRFDKGFTVFFDVFPEYSGWNNFLGREICVEAFQVKKEDITGKEKDTTGKKTLIPIKKEPLTLKVPTDIDLKDVLRYIFLNMDPEQRKLKATKESEDIFNDIKATYNKLHNELERSKK
>NZ_CP024593.1|WP_012458620.1|1058410_1058647_-|hypothetical-protein
MEIETLILLSLAVAGFTTIIVVAIVWYSKFKIRKEELEHQRLVEQEREKAKELNNSFAKSLLATNKEIIEVYCKNNTK
>NZ_CP024593.1|WP_012458621.1|1058648_1060232_-|hypothetical-protein
MEAETYSRHIFIFPFQWDYIEKRGYASYNERTDIKKFDKLFSAVSPLKRQYFEIGASEERYNEYTYFHPFARRALFGTKENPSVYHYELSDTQGTYNISVKIDGVSTTYSLQLEKIAVSVFDTGVGTVAYFLRNDKHTSFEDILRINDTGRRIYPQYMAKGNRLKAKDSFLADRIYGSLGVLDFDDDFRQFEEDISHTNIFLPPDHIRQVFGYNKMDRTEDDGCQKFVFHQESERKDIIRISPVMDDRMFFITYYHSPYYAKKLRSKPKNFRRKREYNIYEEGHFGDLWFRYLFGDGGDKTVANTSVQREDVRRTTYARWSGSGTLFGLTKDSLVGISDWYLIGDHITTMYYQMATLSLVQRSTILRFSNEIASITQLILDKKTKRKTEKQVKELYGNYIRFLNETYFREVTPQIQGIEMYDMLQSNMNIEKDAKALDEEMGELFNYTTLEEQGVLNKTANLYLPITLLVGFLGINTFVEKGCITRFFNIGDPCPSTWGLLGGDIITLIVFAICLYFPIRHYFKYRK

Crispr_ID: NZ_CP024593_6

• CRISPR_ID: NZ_CP024593_6
• CRISPR_location: 1081972-1091801
• CRISPR_type: Unclear
• Repeat_type: NA
• Spacer_info: 147 spacers
• Cas_protein_info: cas2,cas1,cas4,cas3,cas7b,cas8b4,cas5,cas6

Consensus repeat of NZ_CP024593_6

Consensus_repeat	Method
ATTTTAATTCCTGTATGGTGCAATTGAAAT	PILER-CR
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CRISPRCasFinder
NNNNNANNNNNNNATTTTAATTCCTGTATGGTGCAATTGAAAT	CRT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CRT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	PILER-CR
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CRISPRCasFinder

spacers of NZ_CP024593_6

>6.1|1082002|38|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
GATATCGGAGGTGTCGACATGTCGGAGGTCGTATCTGT
>6.2|1082070|36|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
GGTCGAGCGCCTTACACAGGCGGGCGAGCATGTCGA
>6.3|1082136|35|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
CCCAGCCACACGCTGATACGGTTATATCGCAGCTC
>6.4|1082201|35|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
TACCCAGCCCCAATCGAACGTAACCCCCGACGTCA
>6.5|1082266|38|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
CTGGTGGGAGACGAAGATGATTTCTTCAATATAATTAA
>6.6|1082334|35|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
AGTGGGCAACGATATTTTCCATCATGAGTGCTTTC
>6.7|1082399|35|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
CGCCGCAGGCATCAAGGCTACGAAGCGCAACGCAG
>6.8|1082464|37|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
AACCTCCATCAGCGCTTTTTTCTCGGCCGTCAAGGCC
>6.9|1082531|34|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
GAGCCTCGATGCATCCCGAGGCGGAAGCCAGCCT
>6.10|1082595|37|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
AGAGACTTGTGTCTGATTGTCTGTGCAATTATTTTGT
>6.11|1082662|34|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
CGATCAGCTGCATAATCTGGTCGTTGATGGCGTC
>6.12|1082726|36|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
CGAGGCGGACAACCCGGCCGTCAAGGCGGATCAGAT
>6.13|1082792|36|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
AGCGATTGGGTACACCTTGTTGTCGAAGAGCACCTC
>6.14|1082858|36|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
AGGCGAAAGAGGAAAAGAGGTCTCTTTCACAGGAAG
>6.15|1082924|36|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
CACCTTTACCGCGCTGGGGCGGGGCCAGTCGCCCCG
>6.16|1082990|36|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
GCTCTATAAGAGCATTATCGAGGGCGGAAAGTTGTT
>6.17|1083056|36|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
CGCCGCTGGCACACCTCCCCCGTGTCAAAAGGGGGG
>6.18|1083122|35|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
ATGTCGAGATCGATCAGCATCCTGATCACCACCTC
>6.19|1083187|36|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
CTTCAAACTTCGCGTACCCCTTGCCCGACTCCGCTT
>6.20|1083253|35|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
GCAGTAGACGATAGAAGCCTGCGTGTCTGTTGCCC
>6.21|1083318|36|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
GACCCATCGAAGCACGCGGATATCACCTTCGCCGAA
>6.22|1083384|36|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
TTGTACCCACGTGCACGCTGAATAACCACAAGGTCT
>6.23|1083450|37|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
TGTCAATATGCCGGCGATTTGATCCCAGATGCTTCAC
>6.24|1083517|36|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
ACAGCCATCGAATGTCCATTGAGTCGAACGTGCATA
>6.25|1083583|36|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
GTTAGGAGGTAGCCGTGCCCGGGGCGGGTGGCTATA
>6.26|1083649|37|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
GCAATTTCCTTTGCGATGCCGATTCGTTCCTCCCCTT
>6.27|1083716|37|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT
TATCCGCCTCGCCAAATTGGCGCGCGGAATAACAGAG
>6.28|1083783|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
GCTGATATCCCCCACCAGCAGCATGCTTAATTCCTT
>6.29|1083849|35|NZ_CP024593|PILER-CR,CRISPRCasFinder
TGCTTCTGTCATCCGGCAAATTAGAATACTTGAGC
>6.30|1083914|37|NZ_CP024593|PILER-CR,CRISPRCasFinder
AGCGCGCCATCCCTGAAGTGCCCGGCAAGGCATTTAT
>6.31|1083981|35|NZ_CP024593|PILER-CR,CRISPRCasFinder
CTTGTGTAGAAATTTGTCGTTGGCGCGATGAGGAA
>6.32|1084046|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
TGGTTCTAAGCCCACAAAGATATTCCCAAACAAAGT
>6.33|1084112|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
CCATGCGTGCTCAGGAATCTATCCAGTTGCTCCTTG
>6.34|1084178|37|NZ_CP024593|PILER-CR,CRISPRCasFinder
ATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTA
>6.35|1084245|37|NZ_CP024593|PILER-CR,CRISPRCasFinder
ATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTA
>6.36|1084312|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
AGCTCGAGCCGGAGATGGGATACGTGGATGATTCTA
>6.37|1084378|35|NZ_CP024593|PILER-CR,CRISPRCasFinder
GCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGA
>6.38|1084443|35|NZ_CP024593|PILER-CR,CRISPRCasFinder
GCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGA
>6.39|1084508|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
GGCGACCGGGTACACATTATTGTCGAATAGCACGTC
>6.40|1084574|35|NZ_CP024593|PILER-CR,CRISPRCasFinder
TCAATTTTGTTGTCAATTTCCCGTTCTTGGCCCAA
>6.41|1084639|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
CCATGAATTGAGGAAGAGGGGCTATTTTATAAAGAA
>6.42|1084705|37|NZ_CP024593|PILER-CR,CRISPRCasFinder
TCGAGATTTTTTTGTTTGGGAAAAAAGAATCTCCGTA
>6.43|1084772|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
CTTGCTCTAATGAGCCTAAGCCTGTAGAAGAAACAA
>6.44|1084838|37|NZ_CP024593|PILER-CR,CRISPRCasFinder
ATTGTCAAATAGAAGAATCGGCTTAGCGTTGTAAAAG
>6.45|1084905|37|NZ_CP024593|PILER-CR,CRISPRCasFinder
TCGAGGAACTGTGCATATACAAGCATATTTTCCCGAC
>6.46|1084972|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
GCGTTTGTGCCAATTTTTTCCAAACTGGAAAAATTC
>6.47|1085038|35|NZ_CP024593|PILER-CR,CRISPRCasFinder
TGGAATCTCCTTTGATCCCATAGTTGTTTTTTGTC
>6.48|1085103|34|NZ_CP024593|PILER-CR,CRISPRCasFinder
ACCAAGATGTCAAGAAGTCCATCATGATGATTGT
>6.49|1085167|34|NZ_CP024593|PILER-CR,CRISPRCasFinder
TCGAACGCCTGTACATCGGCTATCTGAATACCGA
>6.50|1085231|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
CTTGTAGAACTCGCTGACATCGATAAGCCAACCCGA
>6.51|1085297|35|NZ_CP024593|PILER-CR,CRISPRCasFinder
CTCCTCCATCGAATCGGGTATCTTGATCTCCACGT
>6.52|1085362|37|NZ_CP024593|PILER-CR,CRISPRCasFinder
TTCGAGGACGAAGAAGGGAACGCCGTCGTTCTGAACA
>6.53|1085429|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
AGGGATTATTGAATATTGTGGAGAAGCTATATCAGA
>6.54|1085495|34|NZ_CP024593|PILER-CR,CRISPRCasFinder
CGGAAAAACAGAGGAGGAGATTGGATGACGGCTG
>6.55|1085559|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
ACAAGAAGATTCTCGACGCTCTCTACAATGAGAAGC
>6.56|1085625|35|NZ_CP024593|PILER-CR,CRISPRCasFinder
TTCCTGTGAAGCCGACCACCCGTCCTGTAACAGTG
>6.57|1085690|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
CATAAGATGGAAGTGGCAAAGGCGAAAATAGACGAA
>6.58|1085756|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
TGGGGGCTTTTTACGCACACTATATCGCAGAGCATA
>6.59|1085822|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
CTCCACCGTTACCGTACCCGCCTCGCGGCGCACAAC
>6.60|1085888|37|NZ_CP024593|PILER-CR,CRISPRCasFinder
ATATTGCCCGATTCAGGCGTATGAGGGGTACGACAGC
>6.61|1085955|36|NZ_CP024593|PILER-CR,CRISPRCasFinder
CCTCGATGAACTCCACCCCTGTCACGCCCAGCTCGG
>6.62|1086021|36|NZ_CP024593|CRISPRCasFinder
AAAGCGGAGCTGGTACAAGACACGCACGGGCAAAGG
>6.63|1086087|36|NZ_CP024593|CRISPRCasFinder
TGTGTGTGTGTGTGTGATTTTAATTCCTGTATGGTG
>6.64|1083783|23|NZ_CP024593|CRT
GCTGATATCCCCCACCAGCAGCA
>6.65|1083836|35|NZ_CP024593|CRT
GTGCAATTGAAATTGCTTCTGTCATCCGGCAAATT
>6.66|1083901|37|NZ_CP024593|CRT
GTGCAATTGAAATAGCGCGCCATCCCTGAAGTGCCCG
>6.67|1083968|35|NZ_CP024593|CRT
GTGCAATTGAAATCTTGTGTAGAAATTTGTCGTTG
>6.68|1084033|36|NZ_CP024593|CRT
GTGCAATTGAAATTGGTTCTAAGCCCACAAAGATAT
>6.69|1086133|36|NZ_CP024593|CRT
CTGTATGGTGCAATTGAAATGCAATTTCCTTTGCGA
>6.70|1086199|37|NZ_CP024593|CRT,PILER-CR
TTCAACCTCCGCCCCGGCCTCCCCGTCAGCAATCAGA
>6.71|1086266|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TGTTGCTGCCACGGGTTATTGGGGTCGAACACACC
>6.72|1086331|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TCGAAAGCTCCCGGAAGTATCTTCTCCCTAAATCCG
>6.73|1086397|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CAGGAACAGGCGATCAGGGAAGAGATAGCGAGGATAC
>6.74|1086464|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
AGAATTATCTCAGGCTCTTAGCGAAGAGGGATTTGT
>6.75|1086530|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GGCTTCCTCCTGTAAGGCCCGTTCCTCCTCCGTGTA
>6.76|1086596|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CCCAAGCCCGAACGGTAGCACTGCCACAAGCCCGAA
>6.77|1086662|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TACTGTTACAATTTTGTCTGTTTTAAGTTTTACAG
>6.78|1086727|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GTATTTGTCTCTTGACTAACCCCGTGATAGCGTCAAG
>6.79|1086794|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CTCAACACGTCGGAGGAGGGCCTTGTGTTCGCCAAC
>6.80|1086860|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
ACGCTGGAAAAAGATTACTCGGTTTCGGGAAAGGTT
>6.81|1086926|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
AGGCTTGCCCGTCTTTCGATGTTCCTCGCTGGCTAA
>6.82|1086992|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
ATGGAAATGCTATTGCAGATTGTACAGATACTATT
>6.83|1087057|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TCGGCTGTGGGGGTAGAGCCATGCCGTGCTTCAGCA
>6.84|1087123|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GCGGAGGAATCGAACCTCCGTATAGAACTATCTAC
>6.85|1087188|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CACAAGCGTGCATGGTCTCGACGAGAAGCAGGAGCT
>6.86|1087254|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
ATGTGTTTGTCACCGCCCCAGGCATGACTGCTACGA
>6.87|1087320|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TAGTTACAAAACATAAACAAGAAAAAAGAATTTTCAT
>6.88|1087387|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CCCTCGAGCCGGGCGCAACGGTTGCCGATGCCAGAAA
>6.89|1087454|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TACGGTAAGCCCCGCCAAGGATATGTGGAAGTGCTT
>6.90|1087520|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
AGATACTCAATCGCTATGAGACCGGATATGCTCCTGC
>6.91|1087587|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
AGATTGGATGCTTCTCAACAAATGTTTCTTACTTC
>6.92|1087652|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TGTTTGGAAATCAACTCAGTCTTAATGTTATTACAGA
>6.93|1087719|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TATTTCTATAAGTAAGTTTTTTGTTAACTATACGTC
>6.94|1087785|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TTCCCTACGACCGAAACGGGAACACTCTCTTTTACA
>6.95|1087851|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TATTTCTATAAGTAAGTTTTTTGTTAACTATACGTC
>6.96|1087917|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TTCCCTACGACCGAAACGGGAACACTCTCTTTTACA
>6.97|1087983|34|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
AAAGATGAATCCGGGTAGGGCATACTCGTGAAGT
>6.98|1088047|34|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TAAAACAAAAAATTTTAGAGATTATGTTACGATC
>6.99|1088111|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
ATTGTTGCCGCCAGCCCACCGACTCCACCCGCCGTA
>6.100|1088177|39|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GCTCGGGTTGTGCGCTCGGGTTGGGAACGATGCTGCACG
>6.101|1088246|38|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GGACAATTCTTGCTCCGCCGAGGCGGGCTTAAGCACCT
>6.102|1088314|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GCCAGCTTCTTGGCTTCTTGGCGCGCTTGGATAACCT
>6.103|1088381|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TTTTTGGAAGATGTATCGTGGAGAGGTGCGGGCTT
>6.104|1088446|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CATGCCCCTTCCACGCGGATAACAACGCTTCTCTGA
>6.105|1088512|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GCCACAGCCCGAAGAGCACCCGTCCCTTGCTGAAGAG
>6.106|1088579|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GAGCAGCTGCGCAATGGGTGGAATCCGTTTATTGAAG
>6.107|1088646|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CGTAACCGCCTCTGTAGACCGCTCCACGCAGTCGTT
>6.108|1088712|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TATTTAACGACGAGGACGGCGTGCGCAAGGCGGAGC
>6.109|1088778|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TCGTTATGACGGGCGACTGTATCCCTTGCGTTTACA
>6.110|1088844|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
AACCAGTTTGGGCTGGAGGCGTCGGAGGCGGCACGGG
>6.111|1088911|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
AATACAAGAAAGTACTCGTGCTGTCGACCCTAAAAT
>6.112|1088977|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
AAACCGCCGACGGAGCACCGGCCGGCACCATCCGCA
>6.113|1089043|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CCTCCGACCCCTTTTGGGCCGAGTACTACCCGCCCAA
>6.114|1089110|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GGCCGAGGCGTTCGCCAAATCGTGGAGGCGCGGAA
>6.115|1089175|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CCGCGTATATAACAACGCGGAGATAACCGTATCGC
>6.116|1089240|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GTGGAGGGCCTCGGAGCGCATTTTTTTCAGATTCA
>6.117|1089305|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TTCATTCCGTATCTTCTGACTATACGTCAAAAGATA
>6.118|1089371|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
ATTGTGCACCCCCTTGCGGTCGCATGGGGGTACACC
>6.119|1089437|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CAAACTTGTCGTCGTAGCTATCAAGGCTACAACGAT
>6.120|1089503|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TTTCAGCGAGGTCTACCACCTCCGCGCCGCCTGCA
>6.121|1089568|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CGAGCAGGCTGGAGTGCAGCCTTGGAATTTTTGTTT
>6.122|1089634|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
ACGAGGCCCGGCAGCGCAGCAATGCCATCGAAGACG
>6.123|1089700|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TGTAAGTATTGCGACTCAGTAGATACAAGAATTGA
>6.124|1089765|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
ACGCTCGACGAGGGGGTACTGTACCCATATTGATTG
>6.125|1089831|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CATGTCGGAGGAAGCTTCCTTCTTCAATCTCAATCT
>6.126|1089897|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CGCTCATGGCAGGTTATCCGTGAACTGACAGGAGGAA
>6.127|1089964|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
ATGATGAAAAAGATAAGTCCAGCTCTAATCCAGAAGA
>6.128|1090031|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
AAACATGTCGTCGTAGCTATCAAGGCTATAACGAC
>6.129|1090096|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CTCCTGCCCCGGTGGATATATTCTTGAGTGCCGTA
>6.130|1090161|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GCACAGCGTTTGTGCCACCAACCCTTGAAGAAGTTA
>6.131|1090227|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
ATTCGGAGGGCCTAATCGAGAGCGAGGAACGACTGC
>6.132|1090293|34|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CTGCCAGCGGGAATGTCTGTGGCAGATTTTAGAA
>6.133|1090357|34|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GCACTTGATAGACGCGCTTTCCGGAAAAGGCACA
>6.134|1090421|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TCCGGAGGCGTTCCATGACGGCCTTTTCCTCCTCTG
>6.135|1090487|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CTGTACCTCTCATAAAGGAATACAGGGATCTATTTA
>6.136|1090553|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
ACGAATGGGCGCGCGGGATGGCGAAATCGTCCAATA
>6.137|1090619|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GACGTGCAGCTGGAGATCGAGGAAAACACCGCCTTG
>6.138|1090685|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GAAACCAACGCGCTAATTATCAGCGCGTTAGTTTT
>6.139|1090750|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TCACTACGATATAATAGAGTGGCTGCAGCCTGATT
>6.140|1090815|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TCCCGGACTGGCGATTTACGCCGATCCGGATTCGTC
>6.141|1090881|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TGCAGCTGATCGGAACGGGTAATATCCGCTGCATCG
>6.142|1090947|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TCCGCTCTTTTACGAGCGTGCAGACGGCCCTCAATG
>6.143|1091013|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TTGCGACCTGTGAGAGTGCACCTTTTCACCTGTCCG
>6.144|1091079|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
AGAATACGGTCGTGCGCAATATCGAGGCGATGGAGCT
>6.145|1091146|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CGCAAATGTCGCTGATAATCGCGGGTGCCCAACTC
>6.146|1091211|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
ACTCTCAATCAGCACGGGAATCAGATAAATCAGCA
>6.147|1091276|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
CATCCATTCTCGTGTCCACTCAGCAACAGTACCTGC
>6.148|1091342|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TATAAAGAAGAGGAATAGATATGAAGCTAAAGTATT
>6.149|1091408|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
GGGTGGAAGCAGGTCGGATATACGGACATGATCCACT
>6.150|1091475|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TGACCAGAAACCATGCGGGGGTGGGTGCCCAAAGG
>6.151|1091540|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TCTCTGACAAGGTGGCAAACCTGTACGAGGAAGCAA
>6.152|1091606|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
AAAGGAGATAGCTCCTTTTTTATTTGGGCTATCTCT
>6.153|1091672|34|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
TTTCAATGGAATAGAATCAAGCAGGGCTACCAAT
>6.154|1091736|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder
AGGTGATGAAAAATCACTGGAAGAGGCAGTTCAGTA

CRISPR arrays and Neighbor proteins around NZ_CP024593_6

CRISPR arrays

The CRISPR arrays of NZ_CP024593_6

>merge|NZ_CP024593|6|1081972-1091801|PILER-CR,CRISPRCasFinder,CRT,CRT,PILER-CR,CRISPRCasFinder
ATTTTAATTCCTGTATGGTGCAATTGAAATGATATCGGAGGTGTCGACATGTCGGAGGTCGTATCTGTGTTTTAATTCCTGTATGGTGCAATTGAAATGGTCGAGCGCCTTACACAGGCGGGCGAGCATGTCGACTTTTAATTCCTGTATGGTGCAATTGAAATCCCAGCCACACGCTGATACGGTTATATCGCAGCTCATTTTAATTCCTGTATGGTGCAATTGAAATTACCCAGCCCCAATCGAACGTAACCCCCGACGTCAATTTTAATTCCTGTATGGTGCAATTGAAATCTGGTGGGAGACGAAGATGATTTCTTCAATATAATTAAATTTTAATTCCTGTATGGTGCAATTGAAATAGTGGGCAACGATATTTTCCATCATGAGTGCTTTCATTTTAATTCCTGTATGGTGCAATTGAAATCGCCGCAGGCATCAAGGCTACGAAGCGCAACGCAGATTTTAATTCCTGTATGGTGCAATTGAAATAACCTCCATCAGCGCTTTTTTCTCGGCCGTCAAGGCCATTTTAATTCCTGTATGGTGCAATTGAAATGAGCCTCGATGCATCCCGAGGCGGAAGCCAGCCTATTTTAATTCCTGTATGGTGCAATTGAAATAGAGACTTGTGTCTGATTGTCTGTGCAATTATTTTGTATTTTAATTCCTGTATGGTGCAATTGAAATCGATCAGCTGCATAATCTGGTCGTTGATGGCGTCATTTTAATTCCTGTATGGTGCAATTGAAATCGAGGCGGACAACCCGGCCGTCAAGGCGGATCAGATATTTTAATTCCTGTATGGTGCAATTGAAATAGCGATTGGGTACACCTTGTTGTCGAAGAGCACCTCATTTTAATTCCTGTATGGTGCAATTGAAATAGGCGAAAGAGGAAAAGAGGTCTCTTTCACAGGAAGATTTTAATTCCTGTATGGTGCAATTGAAATCACCTTTACCGCGCTGGGGCGGGGCCAGTCGCCCCGATTTTAATTCCTGTATGGTGCAATTGAAATGCTCTATAAGAGCATTATCGAGGGCGGAAAGTTGTTATTTTAATTCCTGTATGGTGCAATTGAAATCGCCGCTGGCACACCTCCCCCGTGTCAAAAGGGGGGATTTTAATTCCTGTATGGTGCAATTGAAATATGTCGAGATCGATCAGCATCCTGATCACCACCTCATTTTAATTCCTGTATGGTGCAATTGAAATCTTCAAACTTCGCGTACCCCTTGCCCGACTCCGCTTATTTTAATTCCTGTATGGTGCAATTGAAATGCAGTAGACGATAGAAGCCTGCGTGTCTGTTGCCCATTTTAATTCCTGTATGGTGCAATTGAAATGACCCATCGAAGCACGCGGATATCACCTTCGCCGAAATTTTAATTCCTGTATGGTGCAATTGAAATTTGTACCCACGTGCACGCTGAATAACCACAAGGTCTATTTTAATTCCTGTATGGTGCAATTGAAATTGTCAATATGCCGGCGATTTGATCCCAGATGCTTCACATTTTAATTCCTGTATGGTGCAATTGAAATACAGCCATCGAATGTCCATTGAGTCGAACGTGCATAATTTTAATTCCTGTATGGTGCAATTGAAATGTTAGGAGGTAGCCGTGCCCGGGGCGGGTGGCTATAATTTTAATTCCTGTATGGTGCAATTGAAATGCAATTTCCTTTGCGATGCCGATTCGTTCCTCCCCTTATTTTAATTCCTGTATGGTGCAATTGAAATTATCCGCCTCGCCAAATTGGCGCGCGGAATAACAGAGATTTTAATTCCTGTATGGTGCAATTGAAATGCTGATATCCCCCACCAGCAGCATGCTTAATTCCTTATTTTAATTCCTGTATGGTGCAATTGAAATTGCTTCTGTCATCCGGCAAATTAGAATACTTGAGCATTTTAATTCCTGTATGGTGCAATTGAAATAGCGCGCCATCCCTGAAGTGCCCGGCAAGGCATTTATATTTTAATTCCTGTATGGTGCAATTGAAATCTTGTGTAGAAATTTGTCGTTGGCGCGATGAGGAAATTTTAATTCCTGTATGGTGCAATTGAAATTGGTTCTAAGCCCACAAAGATATTCCCAAACAAAGTATTTTAATTCCTGTATGGTGCAATTGAAATCCATGCGTGCTCAGGAATCTATCCAGTTGCTCCTTGATTTTAATTCCTGTATGGTGCAATTGAAATATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTAATTTTAATTCCTGTATGGTGCAATTGAAATATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTAATTTTAATTCCTGTATGGTGCAATTGAAATAGCTCGAGCCGGAGATGGGATACGTGGATGATTCTAATTTTAATTCCTGTATGGTGCAATTGAAATGCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGAATTTTAATTCCTGTATGGTGCAATTGAAATGCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGAATTTTAATTCCTGTATGGTGCAATTGAAATGGCGACCGGGTACACATTATTGTCGAATAGCACGTCATTTTAATTCCTGTATGGTGCAATTGAAATTCAATTTTGTTGTCAATTTCCCGTTCTTGGCCCAAATTTTAATTCCTGTATGGTGCAATTGAAATCCATGAATTGAGGAAGAGGGGCTATTTTATAAAGAAATTTTAATTCCTGTATGGTGCAATTGAAATTCGAGATTTTTTTGTTTGGGAAAAAAGAATCTCCGTAATTTTAATTCCTGTATGGTGCAATTGAAATCTTGCTCTAATGAGCCTAAGCCTGTAGAAGAAACAAATTTTAATTCCTGTATGGTGCAATTGAAATATTGTCAAATAGAAGAATCGGCTTAGCGTTGTAAAAGATTTTAATTCCTGTATGGTGCAATTGAAATTCGAGGAACTGTGCATATACAAGCATATTTTCCCGACATTTTAATTCCTGTATGGTGCAATTGAAATGCGTTTGTGCCAATTTTTTCCAAACTGGAAAAATTCATTTTAATTCCTGTATGGTGCAATTGAAATTGGAATCTCCTTTGATCCCATAGTTGTTTTTTGTCATTTTAATTCCTGTATGGTGCAATTGAAATACCAAGATGTCAAGAAGTCCATCATGATGATTGTATTTTAATTCCTGTATGGTGCAATTGAAATTCGAACGCCTGTACATCGGCTATCTGAATACCGAATTTTAATTCCTGTATGGTGCAATTGAAATCTTGTAGAACTCGCTGACATCGATAAGCCAACCCGAATTTTAATTCCTGTATGGTGCAATTGAAATCTCCTCCATCGAATCGGGTATCTTGATCTCCACGTATTTTAATTCCTGTATGGTGCAATTGAAATTTCGAGGACGAAGAAGGGAACGCCGTCGTTCTGAACAATTTTAATTCCTGTATGGTGCAATTGAAATAGGGATTATTGAATATTGTGGAGAAGCTATATCAGAATTTTAATTCCTGTATGGTGCAATTGAAATCGGAAAAACAGAGGAGGAGATTGGATGACGGCTGATTTTAATTCCTGTATGGTGCAATTGAAATACAAGAAGATTCTCGACGCTCTCTACAATGAGAAGCATTTTAATTCCTGTATGGTGCAATTGAAATTTCCTGTGAAGCCGACCACCCGTCCTGTAACAGTGATTTTAATTCCTGTATGGTGCAATTGAAATCATAAGATGGAAGTGGCAAAGGCGAAAATAGACGAAATTTTAATTCCTGTATGGTGCAATTGAAATTGGGGGCTTTTTACGCACACTATATCGCAGAGCATAATTTTAATTCCTGTATGGTGCAATTGAAATCTCCACCGTTACCGTACCCGCCTCGCGGCGCACAACATTTTAATTCCTGTATGGTGCAATTGAAATATATTGCCCGATTCAGGCGTATGAGGGGTACGACAGCATTTTAATTCCTGTATGGTGCAATTGAAATCCTCGATGAACTCCACCCCTGTCACGCCCAGCTCGGATTTTAATTCCTGTATGGTGCAATTGAAATAAAGCGGAGCTGGTACAAGACACGCACGGGCAAAGGATTTTAATTCCTGTATGGTGCAATTGAAATTGTGTGTGTGTGTGTGATTTTAATTCCTGTATGGTGCAATTGAAATCTGTATGGTGCAATTGAAATGCAATTTCCTTTGCGAATTTTAATTCCTGTATGGTGCAATTGAAATTTCAACCTCCGCCCCGGCCTCCCCGTCAGCAATCAGAATTTTAATTCCTGTATGGTGCAATTGAAATTGTTGCTGCCACGGGTTATTGGGGTCGAACACACCATTTTAATTCCTGTATGGTGCAATTGAAATTCGAAAGCTCCCGGAAGTATCTTCTCCCTAAATCCGATTTTAATTCCTGTATGGTGCAATTGAAATCAGGAACAGGCGATCAGGGAAGAGATAGCGAGGATACATTTTAATTCCTGTATGGTGCAATTGAAATAGAATTATCTCAGGCTCTTAGCGAAGAGGGATTTGTATTTTAATTCCTGTATGGTGCAATTGAAATGGCTTCCTCCTGTAAGGCCCGTTCCTCCTCCGTGTAATTTTAATTCCTGTATGGTGCAATTGAAATCCCAAGCCCGAACGGTAGCACTGCCACAAGCCCGAAATTTTAATTCCTGTATGGTGCAATTGAAATTACTGTTACAATTTTGTCTGTTTTAAGTTTTACAGATTTTAATTCCTGTATGGTGCAATTGAAATGTATTTGTCTCTTGACTAACCCCGTGATAGCGTCAAGATTTTAATTCCTGTATGGTGCAATTGAAATCTCAACACGTCGGAGGAGGGCCTTGTGTTCGCCAACATTTTAATTCCTGTATGGTGCAATTGAAATACGCTGGAAAAAGATTACTCGGTTTCGGGAAAGGTTATTTTAATTCCTGTATGGTGCAATTGAAATAGGCTTGCCCGTCTTTCGATGTTCCTCGCTGGCTAAATTTTAATTCCTGTATGGTGCAATTGAAATATGGAAATGCTATTGCAGATTGTACAGATACTATTATTTTAATTCCTGTATGGTGCAATTGAAATTCGGCTGTGGGGGTAGAGCCATGCCGTGCTTCAGCAATTTTAATTCCTGTATGGTGCAATTGAAATGCGGAGGAATCGAACCTCCGTATAGAACTATCTACATTTTAATTCCTGTATGGTGCAATTGAAATCACAAGCGTGCATGGTCTCGACGAGAAGCAGGAGCTATTTTAATTCCTGTATGGTGCAATTGAAATATGTGTTTGTCACCGCCCCAGGCATGACTGCTACGAATTTTAATTCCTGTATGGTGCAATTGAAATTAGTTACAAAACATAAACAAGAAAAAAGAATTTTCATATTTTAATTCCTGTATGGTGCAATTGAAATCCCTCGAGCCGGGCGCAACGGTTGCCGATGCCAGAAAATTTTAATTCCTGTATGGTGCAATTGAAATTACGGTAAGCCCCGCCAAGGATATGTGGAAGTGCTTATTTTAATTCCTGTATGGTGCAATTGAAATAGATACTCAATCGCTATGAGACCGGATATGCTCCTGCATTTTAATTCCTGTATGGTGCAATTGAAATAGATTGGATGCTTCTCAACAAATGTTTCTTACTTCATTTTAATTCCTGTATGGTGCAATTGAAATTGTTTGGAAATCAACTCAGTCTTAATGTTATTACAGAATTTTAATTCCTGTATGGTGCAATTGAAATTATTTCTATAAGTAAGTTTTTTGTTAACTATACGTCATTTTAATTCCTGTATGGTGCAATTGAAATTTCCCTACGACCGAAACGGGAACACTCTCTTTTACAATTTTAATTCCTGTATGGTGCAATTGAAATTATTTCTATAAGTAAGTTTTTTGTTAACTATACGTCATTTTAATTCCTGTATGGTGCAATTGAAATTTCCCTACGACCGAAACGGGAACACTCTCTTTTACAATTTTAATTCCTGTATGGTGCAATTGAAATAAAGATGAATCCGGGTAGGGCATACTCGTGAAGTATTTTAATTCCTGTATGGTGCAATTGAAATTAAAACAAAAAATTTTAGAGATTATGTTACGATCATTTTAATTCCTGTGTGGTGCAATTGAAATATTGTTGCCGCCAGCCCACCGACTCCACCCGCCGTAATTTTAATTCCTGTATGGTGCAATTGAAATGCTCGGGTTGTGCGCTCGGGTTGGGAACGATGCTGCACGATTTTAATTCCTGTATGGTGCAATTGAAATGGACAATTCTTGCTCCGCCGAGGCGGGCTTAAGCACCTATTTTAATTCCTGTATGGTGCAATTGAAATGCCAGCTTCTTGGCTTCTTGGCGCGCTTGGATAACCTATTTTAATTCCTGTATGGTGCAATTGAAATTTTTTGGAAGATGTATCGTGGAGAGGTGCGGGCTTATTTTAATTCCTGTATGGTGCAATTGAAATCATGCCCCTTCCACGCGGATAACAACGCTTCTCTGAATTTTAATTCCTGTATGGTGCAATTGAAATGCCACAGCCCGAAGAGCACCCGTCCCTTGCTGAAGAGATTTTAATTCCTGTATGGTGCAATTGAAATGAGCAGCTGCGCAATGGGTGGAATCCGTTTATTGAAGATTTTAATTCCTGTATGGTGCAATTGAAATCGTAACCGCCTCTGTAGACCGCTCCACGCAGTCGTTATTTTAATTCCTGTATGGTGCAATTGAAATTATTTAACGACGAGGACGGCGTGCGCAAGGCGGAGCATTTTAATTCCTGTATGGTGCAATTGAAATTCGTTATGACGGGCGACTGTATCCCTTGCGTTTACAATTTTAATTCCTGTATGGTGCAATTGAAATAACCAGTTTGGGCTGGAGGCGTCGGAGGCGGCACGGGATTTTAATTCCTGTATGGTGCAATTGAAATAATACAAGAAAGTACTCGTGCTGTCGACCCTAAAATATTTTAATTCCTGTATGGTGCAATTGAAATAAACCGCCGACGGAGCACCGGCCGGCACCATCCGCAATTTTAATTCCTGTATGGTGCAATTGAAATCCTCCGACCCCTTTTGGGCCGAGTACTACCCGCCCAAATTTTAATTCCTGTATGGTGCAATTGAAATGGCCGAGGCGTTCGCCAAATCGTGGAGGCGCGGAAATTTTAATTCCTGTATGGTGCAATTGAAATCCGCGTATATAACAACGCGGAGATAACCGTATCGCATTTTAATTCCTGTATGGTGCAATTGAAATGTGGAGGGCCTCGGAGCGCATTTTTTTCAGATTCAATTTTAATTCCTGTATGGTGCAATTGAAATTTCATTCCGTATCTTCTGACTATACGTCAAAAGATAATTTTAATTCCTGTATGGTGCAATTGAAATATTGTGCACCCCCTTGCGGTCGCATGGGGGTACACCATTTTAATTCCTGTATGGTGCAATTGAAATCAAACTTGTCGTCGTAGCTATCAAGGCTACAACGATATTTTAATTCCTGTATGGTGCAATTGAAATTTTCAGCGAGGTCTACCACCTCCGCGCCGCCTGCAATTTTAATTCCTGTATGGTGCAATTGAAATCGAGCAGGCTGGAGTGCAGCCTTGGAATTTTTGTTTATTTTAATTCCTGTATGGTGCAATTGAAATACGAGGCCCGGCAGCGCAGCAATGCCATCGAAGACGATTTTAATTCCTGTATGGTGCAATTGAAATTGTAAGTATTGCGACTCAGTAGATACAAGAATTGAATTTTAATTCCTGTATGGTGCAATTGAAATACGCTCGACGAGGGGGTACTGTACCCATATTGATTGATTTTAATTCCTGTATGGTGCAATTGAAATCATGTCGGAGGAAGCTTCCTTCTTCAATCTCAATCTATTTTAATTCCTGTATGGTGCAATTGAAATCGCTCATGGCAGGTTATCCGTGAACTGACAGGAGGAAATTTTAATTCCTGTATGGTGCAATTGAAATATGATGAAAAAGATAAGTCCAGCTCTAATCCAGAAGAATTTTAATTCCTGTATGGTGCAATTGAAATAAACATGTCGTCGTAGCTATCAAGGCTATAACGACATTTTAATTCCTGTATGGTGCAATTGAAATCTCCTGCCCCGGTGGATATATTCTTGAGTGCCGTAATTTTAATTCCTGTATGGTGCAATTGAAATGCACAGCGTTTGTGCCACCAACCCTTGAAGAAGTTAATTTTAATTCCTGTATGGTGCAATTGAAATATTCGGAGGGCCTAATCGAGAGCGAGGAACGACTGCATTTTAATTCCTGTATGGTGCAATTGAAATCTGCCAGCGGGAATGTCTGTGGCAGATTTTAGAAATTTTAATTCCTGTATGGTGCAATTGAAATGCACTTGATAGACGCGCTTTCCGGAAAAGGCACAATTTTAATTCCTGTATGGTGCAATTGAAATTCCGGAGGCGTTCCATGACGGCCTTTTCCTCCTCTGATTTTAATTCCTGTATGGTGCAATTGAAATCTGTACCTCTCATAAAGGAATACAGGGATCTATTTAATTTTAATTCCTGTATGGTGCAATTGAAATACGAATGGGCGCGCGGGATGGCGAAATCGTCCAATAATTTTAATTCCTGTATGGTGCAATTGAAATGACGTGCAGCTGGAGATCGAGGAAAACACCGCCTTGATTTTAATTCCTGTATGGTGCAATTGAAATGAAACCAACGCGCTAATTATCAGCGCGTTAGTTTTATTTTAATTCCTGTATGGTGCAATTGAAATTCACTACGATATAATAGAGTGGCTGCAGCCTGATTATTTTAATTCCTGTATGGTGCAATTGAAATTCCCGGACTGGCGATTTACGCCGATCCGGATTCGTCATTTTAATTCCTGTATGGTGCAATTGAAATTGCAGCTGATCGGAACGGGTAATATCCGCTGCATCGATTTTAATTCCTGTATGGTGCAATTGAAATTCCGCTCTTTTACGAGCGTGCAGACGGCCCTCAATGATTTTAATTCCTGTATGGTGCAATTGAAATTTGCGACCTGTGAGAGTGCACCTTTTCACCTGTCCGATTTTAATTCCTGTATGGTGCAATTGAAATAGAATACGGTCGTGCGCAATATCGAGGCGATGGAGCTATTTTAATTCCTGTATGGTGCAATTGAAATCGCAAATGTCGCTGATAATCGCGGGTGCCCAACTCATTTTAATTCCTGTATGGTGCAATTGAAATACTCTCAATCAGCACGGGAATCAGATAAATCAGCAATTTTAATTCCTGTATGGTGCAATTGAAATCATCCATTCTCGTGTCCACTCAGCAACAGTACCTGCATTTTAATTCCTGTATGGTGCAATTGAAATTATAAAGAAGAGGAATAGATATGAAGCTAAAGTATTATTTTAATTCCTGTATGGTGCAATTGAAATGGGTGGAAGCAGGTCGGATATACGGACATGATCCACTATTTTAATTCCTGTATGGTGCAATTGAAATTGACCAGAAACCATGCGGGGGTGGGTGCCCAAAGGATTTTAATTCCTGTATGGTGCAATTGAAATTCTCTGACAAGGTGGCAAACCTGTACGAGGAAGCAAATTTTAATTCCTGTATGGTGCAATTGAAATAAAGGAGATAGCTCCTTTTTTATTTGGGCTATCTCTATTTTAATTCCTGTATGGTGCAATTGAAATTTTCAATGGAATAGAATCAAGCAGGGCTACCAATATTTTAATTCCTGTATGGTGCAATTGAAATAGGTGATGAAAAATCACTGGAAGAGGCAGTTCAGTAATTTTAATTCCTGTATGGTGCAATTGAAAT

>NZ_CP024593|6|3|1081972-1086020|PILER-CR
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GATATCGGAGGTGTCGACATGTCGGAGGTCGTATCTGT
GTTTTAATTCCTGTATGGTGCAATTGAAAT	GGTCGAGCGCCTTACACAGGCGGGCGAGCATGTCGA
CTTTTAATTCCTGTATGGTGCAATTGAAAT	CCCAGCCACACGCTGATACGGTTATATCGCAGCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACCCAGCCCCAATCGAACGTAACCCCCGACGTCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGGTGGGAGACGAAGATGATTTCTTCAATATAATTAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGTGGGCAACGATATTTTCCATCATGAGTGCTTTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCCGCAGGCATCAAGGCTACGAAGCGCAACGCAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AACCTCCATCAGCGCTTTTTTCTCGGCCGTCAAGGCC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAGCCTCGATGCATCCCGAGGCGGAAGCCAGCCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAGACTTGTGTCTGATTGTCTGTGCAATTATTTTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGATCAGCTGCATAATCTGGTCGTTGATGGCGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGAGGCGGACAACCCGGCCGTCAAGGCGGATCAGAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGCGATTGGGTACACCTTGTTGTCGAAGAGCACCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGCGAAAGAGGAAAAGAGGTCTCTTTCACAGGAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CACCTTTACCGCGCTGGGGCGGGGCCAGTCGCCCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTCTATAAGAGCATTATCGAGGGCGGAAAGTTGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCCGCTGGCACACCTCCCCCGTGTCAAAAGGGGGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGTCGAGATCGATCAGCATCCTGATCACCACCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTCAAACTTCGCGTACCCCTTGCCCGACTCCGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCAGTAGACGATAGAAGCCTGCGTGTCTGTTGCCC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GACCCATCGAAGCACGCGGATATCACCTTCGCCGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTGTACCCACGTGCACGCTGAATAACCACAAGGTCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTCAATATGCCGGCGATTTGATCCCAGATGCTTCAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACAGCCATCGAATGTCCATTGAGTCGAACGTGCATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTTAGGAGGTAGCCGTGCCCGGGGCGGGTGGCTATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCAATTTCCTTTGCGATGCCGATTCGTTCCTCCCCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATCCGCCTCGCCAAATTGGCGCGCGGAATAACAGAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTGATATCCCCCACCAGCAGCATGCTTAATTCCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGCTTCTGTCATCCGGCAAATTAGAATACTTGAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGCGCGCCATCCCTGAAGTGCCCGGCAAGGCATTTAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTGTGTAGAAATTTGTCGTTGGCGCGATGAGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGGTTCTAAGCCCACAAAGATATTCCCAAACAAAGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCATGCGTGCTCAGGAATCTATCCAGTTGCTCCTTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGCTCGAGCCGGAGATGGGATACGTGGATGATTCTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCGACCGGGTACACATTATTGTCGAATAGCACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCAATTTTGTTGTCAATTTCCCGTTCTTGGCCCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCATGAATTGAGGAAGAGGGGCTATTTTATAAAGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAGATTTTTTTGTTTGGGAAAAAAGAATCTCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTGCTCTAATGAGCCTAAGCCTGTAGAAGAAACAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTGTCAAATAGAAGAATCGGCTTAGCGTTGTAAAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAGGAACTGTGCATATACAAGCATATTTTCCCGAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCGTTTGTGCCAATTTTTTCCAAACTGGAAAAATTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGGAATCTCCTTTGATCCCATAGTTGTTTTTTGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACCAAGATGTCAAGAAGTCCATCATGATGATTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAACGCCTGTACATCGGCTATCTGAATACCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTGTAGAACTCGCTGACATCGATAAGCCAACCCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCCTCCATCGAATCGGGTATCTTGATCTCCACGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCGAGGACGAAGAAGGGAACGCCGTCGTTCTGAACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGGATTATTGAATATTGTGGAGAAGCTATATCAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGGAAAAACAGAGGAGGAGATTGGATGACGGCTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACAAGAAGATTCTCGACGCTCTCTACAATGAGAAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCTGTGAAGCCGACCACCCGTCCTGTAACAGTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATAAGATGGAAGTGGCAAAGGCGAAAATAGACGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGGGGGCTTTTTACGCACACTATATCGCAGAGCATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCCACCGTTACCGTACCCGCCTCGCGGCGCACAAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATATTGCCCGATTCAGGCGTATGAGGGGTACGACAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCTCGATGAACTCCACCCCTGTCACGCCCAGCTCGG
ATTTTAATTCCTGTATGGTGCAATTGAAATAAAGCGGAGCTGGTACAAGACACGCACGGGCAAAGGATTTTAATTCCTGTATGGTGCAATTGAAATTGTGTGTGTGTGTGTGATTTTAATTCCTGTATGGTGCAATTGAAATCTGTATGGTGCAATTGAAATGCAATTTCCTTTGCGAATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCAACCTCCGCCCCGGCCTCCCCGTCAGCAATCAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTTGCTGCCACGGGTTATTGGGGTCGAACACACC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAAAGCTCCCGGAAGTATCTTCTCCCTAAATCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CAGGAACAGGCGATCAGGGAAGAGATAGCGAGGATAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAATTATCTCAGGCTCTTAGCGAAGAGGGATTTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCTTCCTCCTGTAAGGCCCGTTCCTCCTCCGTGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCCAAGCCCGAACGGTAGCACTGCCACAAGCCCGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACTGTTACAATTTTGTCTGTTTTAAGTTTTACAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTATTTGTCTCTTGACTAACCCCGTGATAGCGTCAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCAACACGTCGGAGGAGGGCCTTGTGTTCGCCAAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGCTGGAAAAAGATTACTCGGTTTCGGGAAAGGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGCTTGCCCGTCTTTCGATGTTCCTCGCTGGCTAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGGAAATGCTATTGCAGATTGTACAGATACTATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGGCTGTGGGGGTAGAGCCATGCCGTGCTTCAGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCGGAGGAATCGAACCTCCGTATAGAACTATCTAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CACAAGCGTGCATGGTCTCGACGAGAAGCAGGAGCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGTGTTTGTCACCGCCCCAGGCATGACTGCTACGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TAGTTACAAAACATAAACAAGAAAAAAGAATTTTCAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCCTCGAGCCGGGCGCAACGGTTGCCGATGCCAGAAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACGGTAAGCCCCGCCAAGGATATGTGGAAGTGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGATACTCAATCGCTATGAGACCGGATATGCTCCTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGATTGGATGCTTCTCAACAAATGTTTCTTACTTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTTTGGAAATCAACTCAGTCTTAATGTTATTACAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTCTATAAGTAAGTTTTTTGTTAACTATACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCCTACGACCGAAACGGGAACACTCTCTTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTCTATAAGTAAGTTTTTTGTTAACTATACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCCTACGACCGAAACGGGAACACTCTCTTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAAGATGAATCCGGGTAGGGCATACTCGTGAAGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TAAAACAAAAAATTTTAGAGATTATGTTACGATC
ATTTTAATTCCTGTGTGGTGCAATTGAAAT	ATTGTTGCCGCCAGCCCACCGACTCCACCCGCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTCGGGTTGTGCGCTCGGGTTGGGAACGATGCTGCACG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGACAATTCTTGCTCCGCCGAGGCGGGCTTAAGCACCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCCAGCTTCTTGGCTTCTTGGCGCGCTTGGATAACCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTTTGGAAGATGTATCGTGGAGAGGTGCGGGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATGCCCCTTCCACGCGGATAACAACGCTTCTCTGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCCACAGCCCGAAGAGCACCCGTCCCTTGCTGAAGAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAGCAGCTGCGCAATGGGTGGAATCCGTTTATTGAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGTAACCGCCTCTGTAGACCGCTCCACGCAGTCGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTAACGACGAGGACGGCGTGCGCAAGGCGGAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGTTATGACGGGCGACTGTATCCCTTGCGTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AACCAGTTTGGGCTGGAGGCGTCGGAGGCGGCACGGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AATACAAGAAAGTACTCGTGCTGTCGACCCTAAAAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAACCGCCGACGGAGCACCGGCCGGCACCATCCGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCTCCGACCCCTTTTGGGCCGAGTACTACCCGCCCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCCGAGGCGTTCGCCAAATCGTGGAGGCGCGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCGCGTATATAACAACGCGGAGATAACCGTATCGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTGGAGGGCCTCGGAGCGCATTTTTTTCAGATTCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCATTCCGTATCTTCTGACTATACGTCAAAAGATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTGTGCACCCCCTTGCGGTCGCATGGGGGTACACC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CAAACTTGTCGTCGTAGCTATCAAGGCTACAACGAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTCAGCGAGGTCTACCACCTCCGCGCCGCCTGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGAGCAGGCTGGAGTGCAGCCTTGGAATTTTTGTTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGAGGCCCGGCAGCGCAGCAATGCCATCGAAGACG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTAAGTATTGCGACTCAGTAGATACAAGAATTGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGCTCGACGAGGGGGTACTGTACCCATATTGATTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATGTCGGAGGAAGCTTCCTTCTTCAATCTCAATCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCTCATGGCAGGTTATCCGTGAACTGACAGGAGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGATGAAAAAGATAAGTCCAGCTCTAATCCAGAAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAACATGTCGTCGTAGCTATCAAGGCTATAACGAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCCTGCCCCGGTGGATATATTCTTGAGTGCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACAGCGTTTGTGCCACCAACCCTTGAAGAAGTTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTCGGAGGGCCTAATCGAGAGCGAGGAACGACTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGCCAGCGGGAATGTCTGTGGCAGATTTTAGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACTTGATAGACGCGCTTTCCGGAAAAGGCACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCGGAGGCGTTCCATGACGGCCTTTTCCTCCTCTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGTACCTCTCATAAAGGAATACAGGGATCTATTTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGAATGGGCGCGCGGGATGGCGAAATCGTCCAATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GACGTGCAGCTGGAGATCGAGGAAAACACCGCCTTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAAACCAACGCGCTAATTATCAGCGCGTTAGTTTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCACTACGATATAATAGAGTGGCTGCAGCCTGATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCCGGACTGGCGATTTACGCCGATCCGGATTCGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGCAGCTGATCGGAACGGGTAATATCCGCTGCATCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCGCTCTTTTACGAGCGTGCAGACGGCCCTCAATG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTGCGACCTGTGAGAGTGCACCTTTTCACCTGTCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAATACGGTCGTGCGCAATATCGAGGCGATGGAGCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCAAATGTCGCTGATAATCGCGGGTGCCCAACTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACTCTCAATCAGCACGGGAATCAGATAAATCAGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATCCATTCTCGTGTCCACTCAGCAACAGTACCTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATAAAGAAGAGGAATAGATATGAAGCTAAAGTATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGGTGGAAGCAGGTCGGATATACGGACATGATCCACT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGACCAGAAACCATGCGGGGGTGGGTGCCCAAAGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCTCTGACAAGGTGGCAAACCTGTACGAGGAAGCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAAGGAGATAGCTCCTTTTTTATTTGGGCTATCTCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTCAATGGAATAGAATCAAGCAGGGCTACCAAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGTGATGAAAAATCACTGGAAGAGGCAGTTCAGTA


>NZ_CP024593|6|6|1081972-1086153|CRISPRCasFinder
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GATATCGGAGGTGTCGACATGTCGGAGGTCGTATCTGT
GTTTTAATTCCTGTATGGTGCAATTGAAAT	GGTCGAGCGCCTTACACAGGCGGGCGAGCATGTCGA
CTTTTAATTCCTGTATGGTGCAATTGAAAT	CCCAGCCACACGCTGATACGGTTATATCGCAGCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACCCAGCCCCAATCGAACGTAACCCCCGACGTCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGGTGGGAGACGAAGATGATTTCTTCAATATAATTAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGTGGGCAACGATATTTTCCATCATGAGTGCTTTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCCGCAGGCATCAAGGCTACGAAGCGCAACGCAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AACCTCCATCAGCGCTTTTTTCTCGGCCGTCAAGGCC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAGCCTCGATGCATCCCGAGGCGGAAGCCAGCCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAGACTTGTGTCTGATTGTCTGTGCAATTATTTTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGATCAGCTGCATAATCTGGTCGTTGATGGCGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGAGGCGGACAACCCGGCCGTCAAGGCGGATCAGAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGCGATTGGGTACACCTTGTTGTCGAAGAGCACCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGCGAAAGAGGAAAAGAGGTCTCTTTCACAGGAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CACCTTTACCGCGCTGGGGCGGGGCCAGTCGCCCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTCTATAAGAGCATTATCGAGGGCGGAAAGTTGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCCGCTGGCACACCTCCCCCGTGTCAAAAGGGGGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGTCGAGATCGATCAGCATCCTGATCACCACCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTCAAACTTCGCGTACCCCTTGCCCGACTCCGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCAGTAGACGATAGAAGCCTGCGTGTCTGTTGCCC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GACCCATCGAAGCACGCGGATATCACCTTCGCCGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTGTACCCACGTGCACGCTGAATAACCACAAGGTCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTCAATATGCCGGCGATTTGATCCCAGATGCTTCAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACAGCCATCGAATGTCCATTGAGTCGAACGTGCATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTTAGGAGGTAGCCGTGCCCGGGGCGGGTGGCTATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCAATTTCCTTTGCGATGCCGATTCGTTCCTCCCCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATCCGCCTCGCCAAATTGGCGCGCGGAATAACAGAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTGATATCCCCCACCAGCAGCATGCTTAATTCCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGCTTCTGTCATCCGGCAAATTAGAATACTTGAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGCGCGCCATCCCTGAAGTGCCCGGCAAGGCATTTAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTGTGTAGAAATTTGTCGTTGGCGCGATGAGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGGTTCTAAGCCCACAAAGATATTCCCAAACAAAGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCATGCGTGCTCAGGAATCTATCCAGTTGCTCCTTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGCTCGAGCCGGAGATGGGATACGTGGATGATTCTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCGACCGGGTACACATTATTGTCGAATAGCACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCAATTTTGTTGTCAATTTCCCGTTCTTGGCCCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCATGAATTGAGGAAGAGGGGCTATTTTATAAAGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAGATTTTTTTGTTTGGGAAAAAAGAATCTCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTGCTCTAATGAGCCTAAGCCTGTAGAAGAAACAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTGTCAAATAGAAGAATCGGCTTAGCGTTGTAAAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAGGAACTGTGCATATACAAGCATATTTTCCCGAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCGTTTGTGCCAATTTTTTCCAAACTGGAAAAATTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGGAATCTCCTTTGATCCCATAGTTGTTTTTTGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACCAAGATGTCAAGAAGTCCATCATGATGATTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAACGCCTGTACATCGGCTATCTGAATACCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTGTAGAACTCGCTGACATCGATAAGCCAACCCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCCTCCATCGAATCGGGTATCTTGATCTCCACGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCGAGGACGAAGAAGGGAACGCCGTCGTTCTGAACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGGATTATTGAATATTGTGGAGAAGCTATATCAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGGAAAAACAGAGGAGGAGATTGGATGACGGCTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACAAGAAGATTCTCGACGCTCTCTACAATGAGAAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCTGTGAAGCCGACCACCCGTCCTGTAACAGTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATAAGATGGAAGTGGCAAAGGCGAAAATAGACGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGGGGGCTTTTTACGCACACTATATCGCAGAGCATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCCACCGTTACCGTACCCGCCTCGCGGCGCACAAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATATTGCCCGATTCAGGCGTATGAGGGGTACGACAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCTCGATGAACTCCACCCCTGTCACGCCCAGCTCGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAAGCGGAGCTGGTACAAGACACGCACGGGCAAAGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTGTGTGTGTGTGTGATTTTAATTCCTGTATGGTG
CAATTGAAATCTGTATGGTGCAATTGAAATGCAATTTCCTTTGCGAATTTTAATTCCTGTATGGTGCAATTGAAATTTCAACCTCCGCCCCGGCCTCCCCGTCAGCAATCAGAATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTTGCTGCCACGGGTTATTGGGGTCGAACACACC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAAAGCTCCCGGAAGTATCTTCTCCCTAAATCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CAGGAACAGGCGATCAGGGAAGAGATAGCGAGGATAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAATTATCTCAGGCTCTTAGCGAAGAGGGATTTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCTTCCTCCTGTAAGGCCCGTTCCTCCTCCGTGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCCAAGCCCGAACGGTAGCACTGCCACAAGCCCGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACTGTTACAATTTTGTCTGTTTTAAGTTTTACAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTATTTGTCTCTTGACTAACCCCGTGATAGCGTCAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCAACACGTCGGAGGAGGGCCTTGTGTTCGCCAAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGCTGGAAAAAGATTACTCGGTTTCGGGAAAGGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGCTTGCCCGTCTTTCGATGTTCCTCGCTGGCTAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGGAAATGCTATTGCAGATTGTACAGATACTATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGGCTGTGGGGGTAGAGCCATGCCGTGCTTCAGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCGGAGGAATCGAACCTCCGTATAGAACTATCTAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CACAAGCGTGCATGGTCTCGACGAGAAGCAGGAGCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGTGTTTGTCACCGCCCCAGGCATGACTGCTACGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TAGTTACAAAACATAAACAAGAAAAAAGAATTTTCAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCCTCGAGCCGGGCGCAACGGTTGCCGATGCCAGAAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACGGTAAGCCCCGCCAAGGATATGTGGAAGTGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGATACTCAATCGCTATGAGACCGGATATGCTCCTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGATTGGATGCTTCTCAACAAATGTTTCTTACTTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTTTGGAAATCAACTCAGTCTTAATGTTATTACAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTCTATAAGTAAGTTTTTTGTTAACTATACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCCTACGACCGAAACGGGAACACTCTCTTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTCTATAAGTAAGTTTTTTGTTAACTATACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCCTACGACCGAAACGGGAACACTCTCTTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAAGATGAATCCGGGTAGGGCATACTCGTGAAGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TAAAACAAAAAATTTTAGAGATTATGTTACGATC
ATTTTAATTCCTGTGTGGTGCAATTGAAAT	ATTGTTGCCGCCAGCCCACCGACTCCACCCGCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTCGGGTTGTGCGCTCGGGTTGGGAACGATGCTGCACG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGACAATTCTTGCTCCGCCGAGGCGGGCTTAAGCACCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCCAGCTTCTTGGCTTCTTGGCGCGCTTGGATAACCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTTTGGAAGATGTATCGTGGAGAGGTGCGGGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATGCCCCTTCCACGCGGATAACAACGCTTCTCTGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCCACAGCCCGAAGAGCACCCGTCCCTTGCTGAAGAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAGCAGCTGCGCAATGGGTGGAATCCGTTTATTGAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGTAACCGCCTCTGTAGACCGCTCCACGCAGTCGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTAACGACGAGGACGGCGTGCGCAAGGCGGAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGTTATGACGGGCGACTGTATCCCTTGCGTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AACCAGTTTGGGCTGGAGGCGTCGGAGGCGGCACGGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AATACAAGAAAGTACTCGTGCTGTCGACCCTAAAAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAACCGCCGACGGAGCACCGGCCGGCACCATCCGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCTCCGACCCCTTTTGGGCCGAGTACTACCCGCCCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCCGAGGCGTTCGCCAAATCGTGGAGGCGCGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCGCGTATATAACAACGCGGAGATAACCGTATCGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTGGAGGGCCTCGGAGCGCATTTTTTTCAGATTCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCATTCCGTATCTTCTGACTATACGTCAAAAGATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTGTGCACCCCCTTGCGGTCGCATGGGGGTACACC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CAAACTTGTCGTCGTAGCTATCAAGGCTACAACGAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTCAGCGAGGTCTACCACCTCCGCGCCGCCTGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGAGCAGGCTGGAGTGCAGCCTTGGAATTTTTGTTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGAGGCCCGGCAGCGCAGCAATGCCATCGAAGACG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTAAGTATTGCGACTCAGTAGATACAAGAATTGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGCTCGACGAGGGGGTACTGTACCCATATTGATTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATGTCGGAGGAAGCTTCCTTCTTCAATCTCAATCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCTCATGGCAGGTTATCCGTGAACTGACAGGAGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGATGAAAAAGATAAGTCCAGCTCTAATCCAGAAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAACATGTCGTCGTAGCTATCAAGGCTATAACGAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCCTGCCCCGGTGGATATATTCTTGAGTGCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACAGCGTTTGTGCCACCAACCCTTGAAGAAGTTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTCGGAGGGCCTAATCGAGAGCGAGGAACGACTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGCCAGCGGGAATGTCTGTGGCAGATTTTAGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACTTGATAGACGCGCTTTCCGGAAAAGGCACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCGGAGGCGTTCCATGACGGCCTTTTCCTCCTCTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGTACCTCTCATAAAGGAATACAGGGATCTATTTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGAATGGGCGCGCGGGATGGCGAAATCGTCCAATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GACGTGCAGCTGGAGATCGAGGAAAACACCGCCTTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAAACCAACGCGCTAATTATCAGCGCGTTAGTTTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCACTACGATATAATAGAGTGGCTGCAGCCTGATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCCGGACTGGCGATTTACGCCGATCCGGATTCGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGCAGCTGATCGGAACGGGTAATATCCGCTGCATCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCGCTCTTTTACGAGCGTGCAGACGGCCCTCAATG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTGCGACCTGTGAGAGTGCACCTTTTCACCTGTCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAATACGGTCGTGCGCAATATCGAGGCGATGGAGCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCAAATGTCGCTGATAATCGCGGGTGCCCAACTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACTCTCAATCAGCACGGGAATCAGATAAATCAGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATCCATTCTCGTGTCCACTCAGCAACAGTACCTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATAAAGAAGAGGAATAGATATGAAGCTAAAGTATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGGTGGAAGCAGGTCGGATATACGGACATGATCCACT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGACCAGAAACCATGCGGGGGTGGGTGCCCAAAGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCTCTGACAAGGTGGCAAACCTGTACGAGGAAGCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAAGGAGATAGCTCCTTTTTTATTTGGGCTATCTCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTCAATGGAATAGAATCAAGCAGGGCTACCAAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGTGATGAAAAATCACTGGAAGAGGCAGTTCAGTA


>NZ_CP024593|6|3|1081972-1084098|CRT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GATATCGGAGGTGTCGACATGTCGGAGGTCGTATCTGT
GTTTTAATTCCTGTATGGTGCAATTGAAAT	GGTCGAGCGCCTTACACAGGCGGGCGAGCATGTCGA
CTTTTAATTCCTGTATGGTGCAATTGAAAT	CCCAGCCACACGCTGATACGGTTATATCGCAGCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACCCAGCCCCAATCGAACGTAACCCCCGACGTCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGGTGGGAGACGAAGATGATTTCTTCAATATAATTAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGTGGGCAACGATATTTTCCATCATGAGTGCTTTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCCGCAGGCATCAAGGCTACGAAGCGCAACGCAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AACCTCCATCAGCGCTTTTTTCTCGGCCGTCAAGGCC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAGCCTCGATGCATCCCGAGGCGGAAGCCAGCCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAGACTTGTGTCTGATTGTCTGTGCAATTATTTTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGATCAGCTGCATAATCTGGTCGTTGATGGCGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGAGGCGGACAACCCGGCCGTCAAGGCGGATCAGAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGCGATTGGGTACACCTTGTTGTCGAAGAGCACCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGCGAAAGAGGAAAAGAGGTCTCTTTCACAGGAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CACCTTTACCGCGCTGGGGCGGGGCCAGTCGCCCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTCTATAAGAGCATTATCGAGGGCGGAAAGTTGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCCGCTGGCACACCTCCCCCGTGTCAAAAGGGGGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGTCGAGATCGATCAGCATCCTGATCACCACCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTCAAACTTCGCGTACCCCTTGCCCGACTCCGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCAGTAGACGATAGAAGCCTGCGTGTCTGTTGCCC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GACCCATCGAAGCACGCGGATATCACCTTCGCCGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTGTACCCACGTGCACGCTGAATAACCACAAGGTCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTCAATATGCCGGCGATTTGATCCCAGATGCTTCAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACAGCCATCGAATGTCCATTGAGTCGAACGTGCATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTTAGGAGGTAGCCGTGCCCGGGGCGGGTGGCTATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCAATTTCCTTTGCGATGCCGATTCGTTCCTCCCCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATCCGCCTCGCCAAATTGGCGCGCGGAATAACAGAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTGATATCCCCCACCAGCAGCA
TGCTTAATTCCTTATTTTAATTCCTGTATG	GTGCAATTGAAATTGCTTCTGTCATCCGGCAAATT
AGAATACTTGAGCATTTTAATTCCTGTATG	GTGCAATTGAAATAGCGCGCCATCCCTGAAGTGCCCG
GCAAGGCATTTATATTTTAATTCCTGTATG	GTGCAATTGAAATCTTGTGTAGAAATTTGTCGTTG
GCGCGATGAGGAAATTTTAATTCCTGTATG	GTGCAATTGAAATTGGTTCTAAGCCCACAAAGATAT
TCCCAAACAAAGTATTTTAATTCCTGTATGGTGCAATTGAAATCCATGCGTGCTCAGGAATCTATCCAGTTGCTCCTTGATTTTAATTCCTGTATGGTGCAATTGAAATATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTAATTTTAATTCCTGTATGGTGCAATTGAAATATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTAATTTTAATTCCTGTATGGTGCAATTGAAATAGCTCGAGCCGGAGATGGGATACGTGGATGATTCTAATTTTAATTCCTGTATGGTGCAATTGAAATGCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGAATTTTAATTCCTGTATGGTGCAATTGAAATGCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGAATTTTAATTCCTGTATGGTGCAATTGAAATGGCGACCGGGTACACATTATTGTCGAATAGCACGTCATTTTAATTCCTGTATGGTGCAATTGAAATTCAATTTTGTTGTCAATTTCCCGTTCTTGGCCCAAATTTTAATTCCTGTATGGTGCAATTGAAATCCATGAATTGAGGAAGAGGGGCTATTTTATAAAGAAATTTTAATTCCTGTATGGTGCAATTGAAATTCGAGATTTTTTTGTTTGGGAAAAAAGAATCTCCGTAATTTTAATTCCTGTATGGTGCAATTGAAATCTTGCTCTAATGAGCCTAAGCCTGTAGAAGAAACAAATTTTAATTCCTGTATGGTGCAATTGAAATATTGTCAAATAGAAGAATCGGCTTAGCGTTGTAAAAGATTTTAATTCCTGTATGGTGCAATTGAAATTCGAGGAACTGTGCATATACAAGCATATTTTCCCGACATTTTAATTCCTGTATGGTGCAATTGAAATGCGTTTGTGCCAATTTTTTCCAAACTGGAAAAATTCATTTTAATTCCTGTATGGTGCAATTGAAATTGGAATCTCCTTTGATCCCATAGTTGTTTTTTGTCATTTTAATTCCTGTATGGTGCAATTGAAATACCAAGATGTCAAGAAGTCCATCATGATGATTGTATTTTAATTCCTGTATGGTGCAATTGAAATTCGAACGCCTGTACATCGGCTATCTGAATACCGAATTTTAATTCCTGTATGGTGCAATTGAAATCTTGTAGAACTCGCTGACATCGATAAGCCAACCCGAATTTTAATTCCTGTATGGTGCAATTGAAATCTCCTCCATCGAATCGGGTATCTTGATCTCCACGTATTTTAATTCCTGTATGGTGCAATTGAAATTTCGAGGACGAAGAAGGGAACGCCGTCGTTCTGAACAATTTTAATTCCTGTATGGTGCAATTGAAATAGGGATTATTGAATATTGTGGAGAAGCTATATCAGAATTTTAATTCCTGTATGGTGCAATTGAAATCGGAAAAACAGAGGAGGAGATTGGATGACGGCTGATTTTAATTCCTGTATGGTGCAATTGAAATACAAGAAGATTCTCGACGCTCTCTACAATGAGAAGCATTTTAATTCCTGTATGGTGCAATTGAAATTTCCTGTGAAGCCGACCACCCGTCCTGTAACAGTGATTTTAATTCCTGTATGGTGCAATTGAAATCATAAGATGGAAGTGGCAAAGGCGAAAATAGACGAAATTTTAATTCCTGTATGGTGCAATTGAAATTGGGGGCTTTTTACGCACACTATATCGCAGAGCATAATTTTAATTCCTGTATGGTGCAATTGAAATCTCCACCGTTACCGTACCCGCCTCGCGGCGCACAACATTTTAATTCCTGTATGGTGCAATTGAAATATATTGCCCGATTCAGGCGTATGAGGGGTACGACAGCATTTTAATTCCTGTATGGTGCAATTGAAATCCTCGATGAACTCCACCCCTGTCACGCCCAGCTCGGATTTTAATTCCTGTATGGTGCAATTGAAATAAAGCGGAGCTGGTACAAGACACGCACGGGCAAAGGATTTTAATTCCTGTATGGTGCAATTGAAATTGTGTGTGTGTGTGTGATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGTATGGTGCAATTGAAATGCAATTTCCTTTGCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCAACCTCCGCCCCGGCCTCCCCGTCAGCAATCAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTTGCTGCCACGGGTTATTGGGGTCGAACACACC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAAAGCTCCCGGAAGTATCTTCTCCCTAAATCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CAGGAACAGGCGATCAGGGAAGAGATAGCGAGGATAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAATTATCTCAGGCTCTTAGCGAAGAGGGATTTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCTTCCTCCTGTAAGGCCCGTTCCTCCTCCGTGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCCAAGCCCGAACGGTAGCACTGCCACAAGCCCGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACTGTTACAATTTTGTCTGTTTTAAGTTTTACAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTATTTGTCTCTTGACTAACCCCGTGATAGCGTCAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCAACACGTCGGAGGAGGGCCTTGTGTTCGCCAAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGCTGGAAAAAGATTACTCGGTTTCGGGAAAGGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGCTTGCCCGTCTTTCGATGTTCCTCGCTGGCTAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGGAAATGCTATTGCAGATTGTACAGATACTATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGGCTGTGGGGGTAGAGCCATGCCGTGCTTCAGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCGGAGGAATCGAACCTCCGTATAGAACTATCTAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CACAAGCGTGCATGGTCTCGACGAGAAGCAGGAGCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGTGTTTGTCACCGCCCCAGGCATGACTGCTACGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TAGTTACAAAACATAAACAAGAAAAAAGAATTTTCAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCCTCGAGCCGGGCGCAACGGTTGCCGATGCCAGAAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACGGTAAGCCCCGCCAAGGATATGTGGAAGTGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGATACTCAATCGCTATGAGACCGGATATGCTCCTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGATTGGATGCTTCTCAACAAATGTTTCTTACTTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTTTGGAAATCAACTCAGTCTTAATGTTATTACAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTCTATAAGTAAGTTTTTTGTTAACTATACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCCTACGACCGAAACGGGAACACTCTCTTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTCTATAAGTAAGTTTTTTGTTAACTATACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCCTACGACCGAAACGGGAACACTCTCTTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAAGATGAATCCGGGTAGGGCATACTCGTGAAGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TAAAACAAAAAATTTTAGAGATTATGTTACGATC
ATTTTAATTCCTGTGTGGTGCAATTGAAAT	ATTGTTGCCGCCAGCCCACCGACTCCACCCGCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTCGGGTTGTGCGCTCGGGTTGGGAACGATGCTGCACG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGACAATTCTTGCTCCGCCGAGGCGGGCTTAAGCACCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCCAGCTTCTTGGCTTCTTGGCGCGCTTGGATAACCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTTTGGAAGATGTATCGTGGAGAGGTGCGGGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATGCCCCTTCCACGCGGATAACAACGCTTCTCTGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCCACAGCCCGAAGAGCACCCGTCCCTTGCTGAAGAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAGCAGCTGCGCAATGGGTGGAATCCGTTTATTGAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGTAACCGCCTCTGTAGACCGCTCCACGCAGTCGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTAACGACGAGGACGGCGTGCGCAAGGCGGAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGTTATGACGGGCGACTGTATCCCTTGCGTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AACCAGTTTGGGCTGGAGGCGTCGGAGGCGGCACGGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AATACAAGAAAGTACTCGTGCTGTCGACCCTAAAAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAACCGCCGACGGAGCACCGGCCGGCACCATCCGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCTCCGACCCCTTTTGGGCCGAGTACTACCCGCCCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCCGAGGCGTTCGCCAAATCGTGGAGGCGCGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCGCGTATATAACAACGCGGAGATAACCGTATCGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTGGAGGGCCTCGGAGCGCATTTTTTTCAGATTCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCATTCCGTATCTTCTGACTATACGTCAAAAGATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTGTGCACCCCCTTGCGGTCGCATGGGGGTACACC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CAAACTTGTCGTCGTAGCTATCAAGGCTACAACGAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTCAGCGAGGTCTACCACCTCCGCGCCGCCTGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGAGCAGGCTGGAGTGCAGCCTTGGAATTTTTGTTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGAGGCCCGGCAGCGCAGCAATGCCATCGAAGACG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTAAGTATTGCGACTCAGTAGATACAAGAATTGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGCTCGACGAGGGGGTACTGTACCCATATTGATTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATGTCGGAGGAAGCTTCCTTCTTCAATCTCAATCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCTCATGGCAGGTTATCCGTGAACTGACAGGAGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGATGAAAAAGATAAGTCCAGCTCTAATCCAGAAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAACATGTCGTCGTAGCTATCAAGGCTATAACGAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCCTGCCCCGGTGGATATATTCTTGAGTGCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACAGCGTTTGTGCCACCAACCCTTGAAGAAGTTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTCGGAGGGCCTAATCGAGAGCGAGGAACGACTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGCCAGCGGGAATGTCTGTGGCAGATTTTAGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACTTGATAGACGCGCTTTCCGGAAAAGGCACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCGGAGGCGTTCCATGACGGCCTTTTCCTCCTCTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGTACCTCTCATAAAGGAATACAGGGATCTATTTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGAATGGGCGCGCGGGATGGCGAAATCGTCCAATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GACGTGCAGCTGGAGATCGAGGAAAACACCGCCTTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAAACCAACGCGCTAATTATCAGCGCGTTAGTTTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCACTACGATATAATAGAGTGGCTGCAGCCTGATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCCGGACTGGCGATTTACGCCGATCCGGATTCGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGCAGCTGATCGGAACGGGTAATATCCGCTGCATCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCGCTCTTTTACGAGCGTGCAGACGGCCCTCAATG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTGCGACCTGTGAGAGTGCACCTTTTCACCTGTCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAATACGGTCGTGCGCAATATCGAGGCGATGGAGCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCAAATGTCGCTGATAATCGCGGGTGCCCAACTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACTCTCAATCAGCACGGGAATCAGATAAATCAGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATCCATTCTCGTGTCCACTCAGCAACAGTACCTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATAAAGAAGAGGAATAGATATGAAGCTAAAGTATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGGTGGAAGCAGGTCGGATATACGGACATGATCCACT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGACCAGAAACCATGCGGGGGTGGGTGCCCAAAGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCTCTGACAAGGTGGCAAACCTGTACGAGGAAGCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAAGGAGATAGCTCCTTTTTTATTTGGGCTATCTCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTCAATGGAATAGAATCAAGCAGGGCTACCAAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGTGATGAAAAATCACTGGAAGAGGCAGTTCAGTA


>NZ_CP024593|6|4|1086103-1091801|CRT
	GATATCGGAGGTGTCGACATGTCGGAGGTCGTATCTGT
GTTTTAATTCCTGTATGGTGCAATTGAAAT	GGTCGAGCGCCTTACACAGGCGGGCGAGCATGTCGA
CTTTTAATTCCTGTATGGTGCAATTGAAAT	CCCAGCCACACGCTGATACGGTTATATCGCAGCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACCCAGCCCCAATCGAACGTAACCCCCGACGTCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGGTGGGAGACGAAGATGATTTCTTCAATATAATTAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGTGGGCAACGATATTTTCCATCATGAGTGCTTTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCCGCAGGCATCAAGGCTACGAAGCGCAACGCAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AACCTCCATCAGCGCTTTTTTCTCGGCCGTCAAGGCC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAGCCTCGATGCATCCCGAGGCGGAAGCCAGCCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAGACTTGTGTCTGATTGTCTGTGCAATTATTTTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGATCAGCTGCATAATCTGGTCGTTGATGGCGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGAGGCGGACAACCCGGCCGTCAAGGCGGATCAGAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGCGATTGGGTACACCTTGTTGTCGAAGAGCACCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGCGAAAGAGGAAAAGAGGTCTCTTTCACAGGAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CACCTTTACCGCGCTGGGGCGGGGCCAGTCGCCCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTCTATAAGAGCATTATCGAGGGCGGAAAGTTGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCCGCTGGCACACCTCCCCCGTGTCAAAAGGGGGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGTCGAGATCGATCAGCATCCTGATCACCACCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTCAAACTTCGCGTACCCCTTGCCCGACTCCGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCAGTAGACGATAGAAGCCTGCGTGTCTGTTGCCC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GACCCATCGAAGCACGCGGATATCACCTTCGCCGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTGTACCCACGTGCACGCTGAATAACCACAAGGTCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTCAATATGCCGGCGATTTGATCCCAGATGCTTCAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACAGCCATCGAATGTCCATTGAGTCGAACGTGCATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTTAGGAGGTAGCCGTGCCCGGGGCGGGTGGCTATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCAATTTCCTTTGCGATGCCGATTCGTTCCTCCCCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATCCGCCTCGCCAAATTGGCGCGCGGAATAACAGAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTGATATCCCCCACCAGCAGCA
TGCTTAATTCCTTATTTTAATTCCTGTATG	GTGCAATTGAAATTGCTTCTGTCATCCGGCAAATT
AGAATACTTGAGCATTTTAATTCCTGTATG	GTGCAATTGAAATAGCGCGCCATCCCTGAAGTGCCCG
GCAAGGCATTTATATTTTAATTCCTGTATG	GTGCAATTGAAATCTTGTGTAGAAATTTGTCGTTG
GCGCGATGAGGAAATTTTAATTCCTGTATG	GTGCAATTGAAATTGGTTCTAAGCCCACAAAGATAT
TCCCAAACAAAGTATTTTAATTCCTGTATGGTGCAATTGAAATCCATGCGTGCTCAGGAATCTATCCAGTTGCTCCTTGATTTTAATTCCTGTATGGTGCAATTGAAATATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTAATTTTAATTCCTGTATGGTGCAATTGAAATATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTAATTTTAATTCCTGTATGGTGCAATTGAAATAGCTCGAGCCGGAGATGGGATACGTGGATGATTCTAATTTTAATTCCTGTATGGTGCAATTGAAATGCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGAATTTTAATTCCTGTATGGTGCAATTGAAATGCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGAATTTTAATTCCTGTATGGTGCAATTGAAATGGCGACCGGGTACACATTATTGTCGAATAGCACGTCATTTTAATTCCTGTATGGTGCAATTGAAATTCAATTTTGTTGTCAATTTCCCGTTCTTGGCCCAAATTTTAATTCCTGTATGGTGCAATTGAAATCCATGAATTGAGGAAGAGGGGCTATTTTATAAAGAAATTTTAATTCCTGTATGGTGCAATTGAAATTCGAGATTTTTTTGTTTGGGAAAAAAGAATCTCCGTAATTTTAATTCCTGTATGGTGCAATTGAAATCTTGCTCTAATGAGCCTAAGCCTGTAGAAGAAACAAATTTTAATTCCTGTATGGTGCAATTGAAATATTGTCAAATAGAAGAATCGGCTTAGCGTTGTAAAAGATTTTAATTCCTGTATGGTGCAATTGAAATTCGAGGAACTGTGCATATACAAGCATATTTTCCCGACATTTTAATTCCTGTATGGTGCAATTGAAATGCGTTTGTGCCAATTTTTTCCAAACTGGAAAAATTCATTTTAATTCCTGTATGGTGCAATTGAAATTGGAATCTCCTTTGATCCCATAGTTGTTTTTTGTCATTTTAATTCCTGTATGGTGCAATTGAAATACCAAGATGTCAAGAAGTCCATCATGATGATTGTATTTTAATTCCTGTATGGTGCAATTGAAATTCGAACGCCTGTACATCGGCTATCTGAATACCGAATTTTAATTCCTGTATGGTGCAATTGAAATCTTGTAGAACTCGCTGACATCGATAAGCCAACCCGAATTTTAATTCCTGTATGGTGCAATTGAAATCTCCTCCATCGAATCGGGTATCTTGATCTCCACGTATTTTAATTCCTGTATGGTGCAATTGAAATTTCGAGGACGAAGAAGGGAACGCCGTCGTTCTGAACAATTTTAATTCCTGTATGGTGCAATTGAAATAGGGATTATTGAATATTGTGGAGAAGCTATATCAGAATTTTAATTCCTGTATGGTGCAATTGAAATCGGAAAAACAGAGGAGGAGATTGGATGACGGCTGATTTTAATTCCTGTATGGTGCAATTGAAATACAAGAAGATTCTCGACGCTCTCTACAATGAGAAGCATTTTAATTCCTGTATGGTGCAATTGAAATTTCCTGTGAAGCCGACCACCCGTCCTGTAACAGTGATTTTAATTCCTGTATGGTGCAATTGAAATCATAAGATGGAAGTGGCAAAGGCGAAAATAGACGAAATTTTAATTCCTGTATGGTGCAATTGAAATTGGGGGCTTTTTACGCACACTATATCGCAGAGCATAATTTTAATTCCTGTATGGTGCAATTGAAATCTCCACCGTTACCGTACCCGCCTCGCGGCGCACAACATTTTAATTCCTGTATGGTGCAATTGAAATATATTGCCCGATTCAGGCGTATGAGGGGTACGACAGCATTTTAATTCCTGTATGGTGCAATTGAAATCCTCGATGAACTCCACCCCTGTCACGCCCAGCTCGGATTTTAATTCCTGTATGGTGCAATTGAAATAAAGCGGAGCTGGTACAAGACACGCACGGGCAAAGGATTTTAATTCCTGTATGGTGCAATTGAAATTGTGTGTGTGTGTGTGATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGTATGGTGCAATTGAAATGCAATTTCCTTTGCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCAACCTCCGCCCCGGCCTCCCCGTCAGCAATCAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTTGCTGCCACGGGTTATTGGGGTCGAACACACC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAAAGCTCCCGGAAGTATCTTCTCCCTAAATCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CAGGAACAGGCGATCAGGGAAGAGATAGCGAGGATAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAATTATCTCAGGCTCTTAGCGAAGAGGGATTTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCTTCCTCCTGTAAGGCCCGTTCCTCCTCCGTGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCCAAGCCCGAACGGTAGCACTGCCACAAGCCCGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACTGTTACAATTTTGTCTGTTTTAAGTTTTACAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTATTTGTCTCTTGACTAACCCCGTGATAGCGTCAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCAACACGTCGGAGGAGGGCCTTGTGTTCGCCAAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGCTGGAAAAAGATTACTCGGTTTCGGGAAAGGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGCTTGCCCGTCTTTCGATGTTCCTCGCTGGCTAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGGAAATGCTATTGCAGATTGTACAGATACTATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGGCTGTGGGGGTAGAGCCATGCCGTGCTTCAGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCGGAGGAATCGAACCTCCGTATAGAACTATCTAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CACAAGCGTGCATGGTCTCGACGAGAAGCAGGAGCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGTGTTTGTCACCGCCCCAGGCATGACTGCTACGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TAGTTACAAAACATAAACAAGAAAAAAGAATTTTCAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCCTCGAGCCGGGCGCAACGGTTGCCGATGCCAGAAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACGGTAAGCCCCGCCAAGGATATGTGGAAGTGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGATACTCAATCGCTATGAGACCGGATATGCTCCTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGATTGGATGCTTCTCAACAAATGTTTCTTACTTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTTTGGAAATCAACTCAGTCTTAATGTTATTACAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTCTATAAGTAAGTTTTTTGTTAACTATACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCCTACGACCGAAACGGGAACACTCTCTTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTCTATAAGTAAGTTTTTTGTTAACTATACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCCTACGACCGAAACGGGAACACTCTCTTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAAGATGAATCCGGGTAGGGCATACTCGTGAAGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TAAAACAAAAAATTTTAGAGATTATGTTACGATC
ATTTTAATTCCTGTGTGGTGCAATTGAAAT	ATTGTTGCCGCCAGCCCACCGACTCCACCCGCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTCGGGTTGTGCGCTCGGGTTGGGAACGATGCTGCACG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGACAATTCTTGCTCCGCCGAGGCGGGCTTAAGCACCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCCAGCTTCTTGGCTTCTTGGCGCGCTTGGATAACCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTTTGGAAGATGTATCGTGGAGAGGTGCGGGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATGCCCCTTCCACGCGGATAACAACGCTTCTCTGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCCACAGCCCGAAGAGCACCCGTCCCTTGCTGAAGAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAGCAGCTGCGCAATGGGTGGAATCCGTTTATTGAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGTAACCGCCTCTGTAGACCGCTCCACGCAGTCGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTAACGACGAGGACGGCGTGCGCAAGGCGGAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGTTATGACGGGCGACTGTATCCCTTGCGTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AACCAGTTTGGGCTGGAGGCGTCGGAGGCGGCACGGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AATACAAGAAAGTACTCGTGCTGTCGACCCTAAAAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAACCGCCGACGGAGCACCGGCCGGCACCATCCGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCTCCGACCCCTTTTGGGCCGAGTACTACCCGCCCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCCGAGGCGTTCGCCAAATCGTGGAGGCGCGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCGCGTATATAACAACGCGGAGATAACCGTATCGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTGGAGGGCCTCGGAGCGCATTTTTTTCAGATTCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCATTCCGTATCTTCTGACTATACGTCAAAAGATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTGTGCACCCCCTTGCGGTCGCATGGGGGTACACC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CAAACTTGTCGTCGTAGCTATCAAGGCTACAACGAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTCAGCGAGGTCTACCACCTCCGCGCCGCCTGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGAGCAGGCTGGAGTGCAGCCTTGGAATTTTTGTTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGAGGCCCGGCAGCGCAGCAATGCCATCGAAGACG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTAAGTATTGCGACTCAGTAGATACAAGAATTGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGCTCGACGAGGGGGTACTGTACCCATATTGATTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATGTCGGAGGAAGCTTCCTTCTTCAATCTCAATCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCTCATGGCAGGTTATCCGTGAACTGACAGGAGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGATGAAAAAGATAAGTCCAGCTCTAATCCAGAAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAACATGTCGTCGTAGCTATCAAGGCTATAACGAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCCTGCCCCGGTGGATATATTCTTGAGTGCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACAGCGTTTGTGCCACCAACCCTTGAAGAAGTTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTCGGAGGGCCTAATCGAGAGCGAGGAACGACTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGCCAGCGGGAATGTCTGTGGCAGATTTTAGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACTTGATAGACGCGCTTTCCGGAAAAGGCACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCGGAGGCGTTCCATGACGGCCTTTTCCTCCTCTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGTACCTCTCATAAAGGAATACAGGGATCTATTTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGAATGGGCGCGCGGGATGGCGAAATCGTCCAATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GACGTGCAGCTGGAGATCGAGGAAAACACCGCCTTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAAACCAACGCGCTAATTATCAGCGCGTTAGTTTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCACTACGATATAATAGAGTGGCTGCAGCCTGATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCCGGACTGGCGATTTACGCCGATCCGGATTCGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGCAGCTGATCGGAACGGGTAATATCCGCTGCATCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCGCTCTTTTACGAGCGTGCAGACGGCCCTCAATG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTGCGACCTGTGAGAGTGCACCTTTTCACCTGTCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAATACGGTCGTGCGCAATATCGAGGCGATGGAGCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCAAATGTCGCTGATAATCGCGGGTGCCCAACTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACTCTCAATCAGCACGGGAATCAGATAAATCAGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATCCATTCTCGTGTCCACTCAGCAACAGTACCTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATAAAGAAGAGGAATAGATATGAAGCTAAAGTATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGGTGGAAGCAGGTCGGATATACGGACATGATCCACT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGACCAGAAACCATGCGGGGGTGGGTGCCCAAAGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCTCTGACAAGGTGGCAAACCTGTACGAGGAAGCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAAGGAGATAGCTCCTTTTTTATTTGGGCTATCTCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTCAATGGAATAGAATCAAGCAGGGCTACCAAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGTGATGAAAAATCACTGGAAGAGGCAGTTCAGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT

>NZ_CP024593|6|4|1086169-1091801|PILER-CR
	GATATCGGAGGTGTCGACATGTCGGAGGTCGTATCTGT
GTTTTAATTCCTGTATGGTGCAATTGAAAT	GGTCGAGCGCCTTACACAGGCGGGCGAGCATGTCGA
CTTTTAATTCCTGTATGGTGCAATTGAAAT	CCCAGCCACACGCTGATACGGTTATATCGCAGCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACCCAGCCCCAATCGAACGTAACCCCCGACGTCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGGTGGGAGACGAAGATGATTTCTTCAATATAATTAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGTGGGCAACGATATTTTCCATCATGAGTGCTTTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCCGCAGGCATCAAGGCTACGAAGCGCAACGCAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AACCTCCATCAGCGCTTTTTTCTCGGCCGTCAAGGCC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAGCCTCGATGCATCCCGAGGCGGAAGCCAGCCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAGACTTGTGTCTGATTGTCTGTGCAATTATTTTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGATCAGCTGCATAATCTGGTCGTTGATGGCGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGAGGCGGACAACCCGGCCGTCAAGGCGGATCAGAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGCGATTGGGTACACCTTGTTGTCGAAGAGCACCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGCGAAAGAGGAAAAGAGGTCTCTTTCACAGGAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CACCTTTACCGCGCTGGGGCGGGGCCAGTCGCCCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTCTATAAGAGCATTATCGAGGGCGGAAAGTTGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCCGCTGGCACACCTCCCCCGTGTCAAAAGGGGGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGTCGAGATCGATCAGCATCCTGATCACCACCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTCAAACTTCGCGTACCCCTTGCCCGACTCCGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCAGTAGACGATAGAAGCCTGCGTGTCTGTTGCCC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GACCCATCGAAGCACGCGGATATCACCTTCGCCGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTGTACCCACGTGCACGCTGAATAACCACAAGGTCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTCAATATGCCGGCGATTTGATCCCAGATGCTTCAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACAGCCATCGAATGTCCATTGAGTCGAACGTGCATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTTAGGAGGTAGCCGTGCCCGGGGCGGGTGGCTATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCAATTTCCTTTGCGATGCCGATTCGTTCCTCCCCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATCCGCCTCGCCAAATTGGCGCGCGGAATAACAGAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTGATATCCCCCACCAGCAGCATGCTTAATTCCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGCTTCTGTCATCCGGCAAATTAGAATACTTGAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGCGCGCCATCCCTGAAGTGCCCGGCAAGGCATTTAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTGTGTAGAAATTTGTCGTTGGCGCGATGAGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGGTTCTAAGCCCACAAAGATATTCCCAAACAAAGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCATGCGTGCTCAGGAATCTATCCAGTTGCTCCTTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGCTCGAGCCGGAGATGGGATACGTGGATGATTCTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCGACCGGGTACACATTATTGTCGAATAGCACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCAATTTTGTTGTCAATTTCCCGTTCTTGGCCCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCATGAATTGAGGAAGAGGGGCTATTTTATAAAGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAGATTTTTTTGTTTGGGAAAAAAGAATCTCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTGCTCTAATGAGCCTAAGCCTGTAGAAGAAACAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTGTCAAATAGAAGAATCGGCTTAGCGTTGTAAAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAGGAACTGTGCATATACAAGCATATTTTCCCGAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCGTTTGTGCCAATTTTTTCCAAACTGGAAAAATTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGGAATCTCCTTTGATCCCATAGTTGTTTTTTGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACCAAGATGTCAAGAAGTCCATCATGATGATTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAACGCCTGTACATCGGCTATCTGAATACCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTGTAGAACTCGCTGACATCGATAAGCCAACCCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCCTCCATCGAATCGGGTATCTTGATCTCCACGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCGAGGACGAAGAAGGGAACGCCGTCGTTCTGAACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGGATTATTGAATATTGTGGAGAAGCTATATCAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGGAAAAACAGAGGAGGAGATTGGATGACGGCTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACAAGAAGATTCTCGACGCTCTCTACAATGAGAAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCTGTGAAGCCGACCACCCGTCCTGTAACAGTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATAAGATGGAAGTGGCAAAGGCGAAAATAGACGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGGGGGCTTTTTACGCACACTATATCGCAGAGCATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCCACCGTTACCGTACCCGCCTCGCGGCGCACAAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATATTGCCCGATTCAGGCGTATGAGGGGTACGACAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCTCGATGAACTCCACCCCTGTCACGCCCAGCTCGG
ATTTTAATTCCTGTATGGTGCAATTGAAATAAAGCGGAGCTGGTACAAGACACGCACGGGCAAAGGATTTTAATTCCTGTATGGTGCAATTGAAATTGTGTGTGTGTGTGTGATTTTAATTCCTGTATGGTGCAATTGAAATCTGTATGGTGCAATTGAAATGCAATTTCCTTTGCGAATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCAACCTCCGCCCCGGCCTCCCCGTCAGCAATCAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTTGCTGCCACGGGTTATTGGGGTCGAACACACC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAAAGCTCCCGGAAGTATCTTCTCCCTAAATCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CAGGAACAGGCGATCAGGGAAGAGATAGCGAGGATAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAATTATCTCAGGCTCTTAGCGAAGAGGGATTTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCTTCCTCCTGTAAGGCCCGTTCCTCCTCCGTGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCCAAGCCCGAACGGTAGCACTGCCACAAGCCCGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACTGTTACAATTTTGTCTGTTTTAAGTTTTACAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTATTTGTCTCTTGACTAACCCCGTGATAGCGTCAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCAACACGTCGGAGGAGGGCCTTGTGTTCGCCAAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGCTGGAAAAAGATTACTCGGTTTCGGGAAAGGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGCTTGCCCGTCTTTCGATGTTCCTCGCTGGCTAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGGAAATGCTATTGCAGATTGTACAGATACTATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGGCTGTGGGGGTAGAGCCATGCCGTGCTTCAGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCGGAGGAATCGAACCTCCGTATAGAACTATCTAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CACAAGCGTGCATGGTCTCGACGAGAAGCAGGAGCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGTGTTTGTCACCGCCCCAGGCATGACTGCTACGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TAGTTACAAAACATAAACAAGAAAAAAGAATTTTCAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCCTCGAGCCGGGCGCAACGGTTGCCGATGCCAGAAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACGGTAAGCCCCGCCAAGGATATGTGGAAGTGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGATACTCAATCGCTATGAGACCGGATATGCTCCTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGATTGGATGCTTCTCAACAAATGTTTCTTACTTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTTTGGAAATCAACTCAGTCTTAATGTTATTACAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTCTATAAGTAAGTTTTTTGTTAACTATACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCCTACGACCGAAACGGGAACACTCTCTTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTCTATAAGTAAGTTTTTTGTTAACTATACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCCTACGACCGAAACGGGAACACTCTCTTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAAGATGAATCCGGGTAGGGCATACTCGTGAAGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TAAAACAAAAAATTTTAGAGATTATGTTACGATC
ATTTTAATTCCTGTGTGGTGCAATTGAAAT	ATTGTTGCCGCCAGCCCACCGACTCCACCCGCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTCGGGTTGTGCGCTCGGGTTGGGAACGATGCTGCACG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGACAATTCTTGCTCCGCCGAGGCGGGCTTAAGCACCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCCAGCTTCTTGGCTTCTTGGCGCGCTTGGATAACCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTTTGGAAGATGTATCGTGGAGAGGTGCGGGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATGCCCCTTCCACGCGGATAACAACGCTTCTCTGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCCACAGCCCGAAGAGCACCCGTCCCTTGCTGAAGAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAGCAGCTGCGCAATGGGTGGAATCCGTTTATTGAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGTAACCGCCTCTGTAGACCGCTCCACGCAGTCGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTAACGACGAGGACGGCGTGCGCAAGGCGGAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGTTATGACGGGCGACTGTATCCCTTGCGTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AACCAGTTTGGGCTGGAGGCGTCGGAGGCGGCACGGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AATACAAGAAAGTACTCGTGCTGTCGACCCTAAAAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAACCGCCGACGGAGCACCGGCCGGCACCATCCGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCTCCGACCCCTTTTGGGCCGAGTACTACCCGCCCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCCGAGGCGTTCGCCAAATCGTGGAGGCGCGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCGCGTATATAACAACGCGGAGATAACCGTATCGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTGGAGGGCCTCGGAGCGCATTTTTTTCAGATTCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCATTCCGTATCTTCTGACTATACGTCAAAAGATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTGTGCACCCCCTTGCGGTCGCATGGGGGTACACC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CAAACTTGTCGTCGTAGCTATCAAGGCTACAACGAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTCAGCGAGGTCTACCACCTCCGCGCCGCCTGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGAGCAGGCTGGAGTGCAGCCTTGGAATTTTTGTTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGAGGCCCGGCAGCGCAGCAATGCCATCGAAGACG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTAAGTATTGCGACTCAGTAGATACAAGAATTGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGCTCGACGAGGGGGTACTGTACCCATATTGATTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATGTCGGAGGAAGCTTCCTTCTTCAATCTCAATCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCTCATGGCAGGTTATCCGTGAACTGACAGGAGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGATGAAAAAGATAAGTCCAGCTCTAATCCAGAAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAACATGTCGTCGTAGCTATCAAGGCTATAACGAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCCTGCCCCGGTGGATATATTCTTGAGTGCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACAGCGTTTGTGCCACCAACCCTTGAAGAAGTTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTCGGAGGGCCTAATCGAGAGCGAGGAACGACTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGCCAGCGGGAATGTCTGTGGCAGATTTTAGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACTTGATAGACGCGCTTTCCGGAAAAGGCACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCGGAGGCGTTCCATGACGGCCTTTTCCTCCTCTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGTACCTCTCATAAAGGAATACAGGGATCTATTTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGAATGGGCGCGCGGGATGGCGAAATCGTCCAATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GACGTGCAGCTGGAGATCGAGGAAAACACCGCCTTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAAACCAACGCGCTAATTATCAGCGCGTTAGTTTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCACTACGATATAATAGAGTGGCTGCAGCCTGATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCCGGACTGGCGATTTACGCCGATCCGGATTCGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGCAGCTGATCGGAACGGGTAATATCCGCTGCATCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCGCTCTTTTACGAGCGTGCAGACGGCCCTCAATG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTGCGACCTGTGAGAGTGCACCTTTTCACCTGTCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAATACGGTCGTGCGCAATATCGAGGCGATGGAGCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCAAATGTCGCTGATAATCGCGGGTGCCCAACTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACTCTCAATCAGCACGGGAATCAGATAAATCAGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATCCATTCTCGTGTCCACTCAGCAACAGTACCTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATAAAGAAGAGGAATAGATATGAAGCTAAAGTATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGGTGGAAGCAGGTCGGATATACGGACATGATCCACT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGACCAGAAACCATGCGGGGGTGGGTGCCCAAAGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCTCTGACAAGGTGGCAAACCTGTACGAGGAAGCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAAGGAGATAGCTCCTTTTTTATTTGGGCTATCTCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTCAATGGAATAGAATCAAGCAGGGCTACCAAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGTGATGAAAAATCACTGGAAGAGGCAGTTCAGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT

>NZ_CP024593|6|7|1086236-1091801|CRISPRCasFinder
	GATATCGGAGGTGTCGACATGTCGGAGGTCGTATCTGT
GTTTTAATTCCTGTATGGTGCAATTGAAAT	GGTCGAGCGCCTTACACAGGCGGGCGAGCATGTCGA
CTTTTAATTCCTGTATGGTGCAATTGAAAT	CCCAGCCACACGCTGATACGGTTATATCGCAGCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACCCAGCCCCAATCGAACGTAACCCCCGACGTCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGGTGGGAGACGAAGATGATTTCTTCAATATAATTAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGTGGGCAACGATATTTTCCATCATGAGTGCTTTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCCGCAGGCATCAAGGCTACGAAGCGCAACGCAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AACCTCCATCAGCGCTTTTTTCTCGGCCGTCAAGGCC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAGCCTCGATGCATCCCGAGGCGGAAGCCAGCCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAGACTTGTGTCTGATTGTCTGTGCAATTATTTTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGATCAGCTGCATAATCTGGTCGTTGATGGCGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGAGGCGGACAACCCGGCCGTCAAGGCGGATCAGAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGCGATTGGGTACACCTTGTTGTCGAAGAGCACCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGCGAAAGAGGAAAAGAGGTCTCTTTCACAGGAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CACCTTTACCGCGCTGGGGCGGGGCCAGTCGCCCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTCTATAAGAGCATTATCGAGGGCGGAAAGTTGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCCGCTGGCACACCTCCCCCGTGTCAAAAGGGGGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGTCGAGATCGATCAGCATCCTGATCACCACCTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTCAAACTTCGCGTACCCCTTGCCCGACTCCGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCAGTAGACGATAGAAGCCTGCGTGTCTGTTGCCC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GACCCATCGAAGCACGCGGATATCACCTTCGCCGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTGTACCCACGTGCACGCTGAATAACCACAAGGTCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTCAATATGCCGGCGATTTGATCCCAGATGCTTCAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACAGCCATCGAATGTCCATTGAGTCGAACGTGCATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTTAGGAGGTAGCCGTGCCCGGGGCGGGTGGCTATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCAATTTCCTTTGCGATGCCGATTCGTTCCTCCCCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATCCGCCTCGCCAAATTGGCGCGCGGAATAACAGAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTGATATCCCCCACCAGCAGCATGCTTAATTCCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGCTTCTGTCATCCGGCAAATTAGAATACTTGAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGCGCGCCATCCCTGAAGTGCCCGGCAAGGCATTTAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTGTGTAGAAATTTGTCGTTGGCGCGATGAGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGGTTCTAAGCCCACAAAGATATTCCCAAACAAAGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCATGCGTGCTCAGGAATCTATCCAGTTGCTCCTTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATCCACTTGCTGCCGTCGCCGGCAGCGTCTACGTGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGCTCGAGCCGGAGATGGGATACGTGGATGATTCTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACCTCTTCGGGATCGAGCACCCCGTCTTCGCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCGACCGGGTACACATTATTGTCGAATAGCACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCAATTTTGTTGTCAATTTCCCGTTCTTGGCCCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCATGAATTGAGGAAGAGGGGCTATTTTATAAAGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAGATTTTTTTGTTTGGGAAAAAAGAATCTCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTGCTCTAATGAGCCTAAGCCTGTAGAAGAAACAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTGTCAAATAGAAGAATCGGCTTAGCGTTGTAAAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAGGAACTGTGCATATACAAGCATATTTTCCCGAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCGTTTGTGCCAATTTTTTCCAAACTGGAAAAATTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGGAATCTCCTTTGATCCCATAGTTGTTTTTTGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACCAAGATGTCAAGAAGTCCATCATGATGATTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAACGCCTGTACATCGGCTATCTGAATACCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTTGTAGAACTCGCTGACATCGATAAGCCAACCCGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCCTCCATCGAATCGGGTATCTTGATCTCCACGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCGAGGACGAAGAAGGGAACGCCGTCGTTCTGAACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGGATTATTGAATATTGTGGAGAAGCTATATCAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGGAAAAACAGAGGAGGAGATTGGATGACGGCTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACAAGAAGATTCTCGACGCTCTCTACAATGAGAAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCTGTGAAGCCGACCACCCGTCCTGTAACAGTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATAAGATGGAAGTGGCAAAGGCGAAAATAGACGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGGGGGCTTTTTACGCACACTATATCGCAGAGCATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCCACCGTTACCGTACCCGCCTCGCGGCGCACAAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATATTGCCCGATTCAGGCGTATGAGGGGTACGACAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCTCGATGAACTCCACCCCTGTCACGCCCAGCTCGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAAGCGGAGCTGGTACAAGACACGCACGGGCAAAGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTGTGTGTGTGTGTGATTTTAATTCCTGTATGGTG
CAATTGAAATCTGTATGGTGCAATTGAAATGCAATTTCCTTTGCGAATTTTAATTCCTGTATGGTGCAATTGAAATTTCAACCTCCGCCCCGGCCTCCCCGTCAGCAATCAGAATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTTGCTGCCACGGGTTATTGGGGTCGAACACACC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGAAAGCTCCCGGAAGTATCTTCTCCCTAAATCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CAGGAACAGGCGATCAGGGAAGAGATAGCGAGGATAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAATTATCTCAGGCTCTTAGCGAAGAGGGATTTGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCTTCCTCCTGTAAGGCCCGTTCCTCCTCCGTGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCCAAGCCCGAACGGTAGCACTGCCACAAGCCCGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACTGTTACAATTTTGTCTGTTTTAAGTTTTACAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTATTTGTCTCTTGACTAACCCCGTGATAGCGTCAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCAACACGTCGGAGGAGGGCCTTGTGTTCGCCAAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGCTGGAAAAAGATTACTCGGTTTCGGGAAAGGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGCTTGCCCGTCTTTCGATGTTCCTCGCTGGCTAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGGAAATGCTATTGCAGATTGTACAGATACTATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGGCTGTGGGGGTAGAGCCATGCCGTGCTTCAGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCGGAGGAATCGAACCTCCGTATAGAACTATCTAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CACAAGCGTGCATGGTCTCGACGAGAAGCAGGAGCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGTGTTTGTCACCGCCCCAGGCATGACTGCTACGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TAGTTACAAAACATAAACAAGAAAAAAGAATTTTCAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCCTCGAGCCGGGCGCAACGGTTGCCGATGCCAGAAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TACGGTAAGCCCCGCCAAGGATATGTGGAAGTGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGATACTCAATCGCTATGAGACCGGATATGCTCCTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGATTGGATGCTTCTCAACAAATGTTTCTTACTTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTTTGGAAATCAACTCAGTCTTAATGTTATTACAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTCTATAAGTAAGTTTTTTGTTAACTATACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCCTACGACCGAAACGGGAACACTCTCTTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTCTATAAGTAAGTTTTTTGTTAACTATACGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCCCTACGACCGAAACGGGAACACTCTCTTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAAGATGAATCCGGGTAGGGCATACTCGTGAAGT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TAAAACAAAAAATTTTAGAGATTATGTTACGATC
ATTTTAATTCCTGTGTGGTGCAATTGAAAT	ATTGTTGCCGCCAGCCCACCGACTCCACCCGCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCTCGGGTTGTGCGCTCGGGTTGGGAACGATGCTGCACG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGACAATTCTTGCTCCGCCGAGGCGGGCTTAAGCACCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCCAGCTTCTTGGCTTCTTGGCGCGCTTGGATAACCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTTTGGAAGATGTATCGTGGAGAGGTGCGGGCTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATGCCCCTTCCACGCGGATAACAACGCTTCTCTGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCCACAGCCCGAAGAGCACCCGTCCCTTGCTGAAGAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAGCAGCTGCGCAATGGGTGGAATCCGTTTATTGAAG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGTAACCGCCTCTGTAGACCGCTCCACGCAGTCGTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATTTAACGACGAGGACGGCGTGCGCAAGGCGGAGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCGTTATGACGGGCGACTGTATCCCTTGCGTTTACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AACCAGTTTGGGCTGGAGGCGTCGGAGGCGGCACGGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AATACAAGAAAGTACTCGTGCTGTCGACCCTAAAAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAACCGCCGACGGAGCACCGGCCGGCACCATCCGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCTCCGACCCCTTTTGGGCCGAGTACTACCCGCCCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGCCGAGGCGTTCGCCAAATCGTGGAGGCGCGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CCGCGTATATAACAACGCGGAGATAACCGTATCGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GTGGAGGGCCTCGGAGCGCATTTTTTTCAGATTCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTCATTCCGTATCTTCTGACTATACGTCAAAAGATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTGTGCACCCCCTTGCGGTCGCATGGGGGTACACC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CAAACTTGTCGTCGTAGCTATCAAGGCTACAACGAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTCAGCGAGGTCTACCACCTCCGCGCCGCCTGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGAGCAGGCTGGAGTGCAGCCTTGGAATTTTTGTTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGAGGCCCGGCAGCGCAGCAATGCCATCGAAGACG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGTAAGTATTGCGACTCAGTAGATACAAGAATTGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGCTCGACGAGGGGGTACTGTACCCATATTGATTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATGTCGGAGGAAGCTTCCTTCTTCAATCTCAATCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCTCATGGCAGGTTATCCGTGAACTGACAGGAGGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATGATGAAAAAGATAAGTCCAGCTCTAATCCAGAAGA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAACATGTCGTCGTAGCTATCAAGGCTATAACGAC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTCCTGCCCCGGTGGATATATTCTTGAGTGCCGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACAGCGTTTGTGCCACCAACCCTTGAAGAAGTTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ATTCGGAGGGCCTAATCGAGAGCGAGGAACGACTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGCCAGCGGGAATGTCTGTGGCAGATTTTAGAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GCACTTGATAGACGCGCTTTCCGGAAAAGGCACA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCGGAGGCGTTCCATGACGGCCTTTTCCTCCTCTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CTGTACCTCTCATAAAGGAATACAGGGATCTATTTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACGAATGGGCGCGCGGGATGGCGAAATCGTCCAATA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GACGTGCAGCTGGAGATCGAGGAAAACACCGCCTTG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GAAACCAACGCGCTAATTATCAGCGCGTTAGTTTT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCACTACGATATAATAGAGTGGCTGCAGCCTGATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCCGGACTGGCGATTTACGCCGATCCGGATTCGTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGCAGCTGATCGGAACGGGTAATATCCGCTGCATCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCCGCTCTTTTACGAGCGTGCAGACGGCCCTCAATG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTGCGACCTGTGAGAGTGCACCTTTTCACCTGTCCG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGAATACGGTCGTGCGCAATATCGAGGCGATGGAGCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CGCAAATGTCGCTGATAATCGCGGGTGCCCAACTC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	ACTCTCAATCAGCACGGGAATCAGATAAATCAGCA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	CATCCATTCTCGTGTCCACTCAGCAACAGTACCTGC
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TATAAAGAAGAGGAATAGATATGAAGCTAAAGTATT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	GGGTGGAAGCAGGTCGGATATACGGACATGATCCACT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TGACCAGAAACCATGCGGGGGTGGGTGCCCAAAGG
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TCTCTGACAAGGTGGCAAACCTGTACGAGGAAGCAA
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AAAGGAGATAGCTCCTTTTTTATTTGGGCTATCTCT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	TTTCAATGGAATAGAATCAAGCAGGGCTACCAAT
ATTTTAATTCCTGTATGGTGCAATTGAAAT	AGGTGATGAAAAATCACTGGAAGAGGCAGTTCAGTA
ATTTTAATTCCTGTATGGTGCAATTGAAAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024593.1|WP_054191585.1|1077893_1078631_+|DNA-repair-protein-RecO	unknown	unknown	gnl|CDD|376822
NZ_CP024593.1|WP_099811786.1|1074146_1074506_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_054191584.1|1078703_1080452_+|phospho-sugar-mutase	unknown	unknown	gnl|CDD|100092
NZ_CP024593.1|WP_005874853.1|1092310_1093327_-|type-I-B-CRISPR-associated-endonuclease-Cas1	cas1	cd09722_cas1_CAS-I-B	gnl|CDD|274695
NZ_CP024593.1|WP_074453431.1|1080711_1081797_-|IS5-family-transposase	unknown	unknown	gnl|CDD|377531
NZ_CP024593.1|WP_081003114.1|1071158_1072502_-|deoxyguanosinetriphosphate-triphosphohydrolase-family-protein	unknown	unknown	gnl|CDD|273571
NZ_CP024593.1|WP_005874854.1|1096166_1097183_-|type-I-PGING-CRISPR-associated-protein-Cas7/Csp1	cas7b	cd09717_cas7b_CAS-I-B	gnl|CDD|132528
NZ_CP024593.1|WP_005874856.1|1099429_1100095_-|CRISPR-associated-endoribonuclease-Cas6	cas6	cd09652_cas6_CAS-I:CAS-III	gnl|CDD|273848
NZ_CP024593.1|WP_013815288.1|1074812_1077314_+|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP024593.1|WP_088442951.1|1072645_1073638_-|putative-sulfate-exporter-family-transporter	unknown	unknown	gnl|CDD|225411
NZ_CP024593.1|WP_005874855.1|1097193_1098693_-|type-I-PGING-CRISPR-associated-protein-Cas8c/Csp2	cas8b4	cd09715_cas8b4_CAS-I-B	gnl|CDD|132526
NZ_CP024593.1|WP_099811787.1|1068969_1070367_-|signal-peptidase-I	unknown	unknown	gnl|CDD|182787
NZ_CP024593.1|WP_099811782.1|1100742_1102674_-|LTA-synthase-family-protein	unknown	unknown	gnl|CDD|293739
NZ_CP024593.1|WP_077070303.1|1098689_1099433_-|type-I-PGING-CRISPR-associated-protein-Cas5p	cas5	cd09716_cas5_CAS-I-B	gnl|CDD|132527
NZ_CP024593.1|WP_005874861.1|1093323_1093836_-|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl|CDD|366863
NZ_CP024593.1|WP_099811788.1|1068353_1068980_-|signal-peptidase-I	unknown	unknown	gnl|CDD|274044
NZ_CP024593.1|WP_005874865.1|1093855_1096177_-|CRISPR-associated-helicase/endonuclease-Cas3	cas3	cd09639_cas3_CAS-I	gnl|CDD|273707
NZ_CP024593.1|WP_143733526.1|1100136_1100406_-|DUF1661-domain-containing-protein	unknown	unknown	gnl|CDD|285160
NZ_CP024593.1|WP_010956473.1|1092047_1092311_-|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl|CDD|187856
NZ_CP024593.1|WP_043894976.1|1070382_1071099_-|4-hydroxy-tetrahydrodipicolinate-reductase	unknown	unknown	gnl|CDD|234595

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP024593.1|WP_005874854.1|1096166_1097183_-|type-I-PGING-CRISPR-associated-protein-Cas7/Csp1	cas7b	cd09717_cas7b_CAS-I-B	9.4e-196	643.5	5.5
NZ_CP024593.1|WP_005874855.1|1097193_1098693_-|type-I-PGING-CRISPR-associated-protein-Cas8c/Csp2	cas8b4	cd09715_cas8b4_CAS-I-B	1.3e-256	846.2	2.1
NZ_CP024593.1|WP_005874865.1|1093855_1096177_-|CRISPR-associated-helicase/endonuclease-Cas3	cas3	cd09639_cas3_CAS-I	8.2e-137	450.7	0.0
NZ_CP024593.1|WP_005874853.1|1092310_1093327_-|type-I-B-CRISPR-associated-endonuclease-Cas1	cas1	cd09722_cas1_CAS-I-B	8e-132	433.9	2.2
NZ_CP024593.1|WP_077070303.1|1098689_1099433_-|type-I-PGING-CRISPR-associated-protein-Cas5p	cas5	cd09716_cas5_CAS-I-B	7.3e-137	448.9	0.7
NZ_CP024593.1|WP_005874861.1|1093323_1093836_-|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	2.4e-53	175.3	0.6
NZ_CP024593.1|WP_005874856.1|1099429_1100095_-|CRISPR-associated-endoribonuclease-Cas6	cas6	cd09652_cas6_CAS-I:CAS-III	9.5e-33	108.9	0.0
NZ_CP024593.1|WP_010956473.1|1092047_1092311_-|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	5.1e-29	95.1	0.2

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP024593.1|WP_054191585.1|1077893_1078631_+|DNA-repair-protein-RecO	gnl|CDD|376822	pfam02565, RecO_C, Recombination protein O C terminal. Recombination protein O (RecO) is involved in DNA repair and pfam00470 pathway recombination.	1.30559e-18
NZ_CP024593.1|WP_081003114.1|1071158_1072502_-|deoxyguanosinetriphosphate-triphosphohydrolase-family-protein	gnl|CDD|273571	TIGR01353, dGTP_triPase, deoxyguanosinetriphosphate triphosphohydrolase, putative. dGTP triphosphohydrolase (dgt) releases inorganic triphosphate, an unusual activity reaction product, from GTP. Its activity has been called limited to the Enterobacteriaceae, although homologous sequences are detected elsewhere. This finding casts doubt on whether the activity is shared in other species. In several of these other species, the homologous gene is found in an apparent operon with dnaG, the DNA primase gene. The enzyme from E. coli was shown to bind coopertatively to single stranded DNA. The biological role of dgt is unknown. [Purines, pyrimidines, nucleosides, and nucleotides, Nucleotide and nucleoside interconversions].	1.29125e-159
NZ_CP024593.1|WP_054191584.1|1078703_1080452_+|phospho-sugar-mutase	gnl|CDD|100092	cd05799, PGM2, This CD includes PGM2 (phosphoglucomutase 2) and PGM2L1 (phosphoglucomutase 2-like 1). The mammalian PGM2 is thought to be a phosphopentomutase that catalyzes the conversion of the nucleoside breakdown products, ribose-1-phosphate and deoxyribose-1-phosphate to the corresponding 5-phosphopentoses. PGM2L1 is thought to catalyze the 1,3-bisphosphoglycerate-dependent synthesis of glucose 1,6-bisphosphate and other aldose-bisphosphates that serve as cofactors for several sugar phosphomutases and possibly also as regulators of glycolytic enzymes. PGM2 and PGM2L1 belong to the alpha-D-phosphohexomutase superfamily which includes several related enzymes that catalyze a reversible intramolecular phosphoryl transfer on their sugar substrates. Other members of this superfamily include phosphoglucosamine mutase (PNGM), phosphoacetylglucosamine mutase (PAGM), the bacterial phosphomannomutase ManB, the bacterial phosphoglucosamine mutase GlmM, and the bifunctional phosphomannomutase/phosphoglucomutase (PMM/PGM). Each of these enzymes has four domains with a centrally located active site formed by four loops, one from each domain. All four domains are included in this alignment model.	0
NZ_CP024593.1|WP_005874853.1|1092310_1093327_-|type-I-B-CRISPR-associated-endonuclease-Cas1	gnl|CDD|274695	TIGR03641, cas1_HMARI, CRISPR-associated endonuclease Cas1, subtype I-B/HMARI/TNEAP. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes Cas1 subgroup that includes Cas1 proteins of the related HMARI and TNEAP subtypes of CRISPR/Cas system.	8.51691e-165
NZ_CP024593.1|WP_074453431.1|1080711_1081797_-|IS5-family-transposase	gnl|CDD|377531	pfam05598, DUF772, Transposase domain (DUF772). This presumed domain is found at the N-terminus of many proteins found in transposons.	2.03613e-23
NZ_CP024593.1|WP_099811782.1|1100742_1102674_-|LTA-synthase-family-protein	gnl|CDD|293739	cd16015, LTA_synthase, Lipoteichoic acid synthase like. Lipoteichoic acid (LTA) is an important cell wall polymer found in Gram-positive bacteria. It may contain long chains of ribitol or glycerol phosphate. LTA synthase catalyzes the reaction to extend the polymer by the repeated addition of glycerolphosphate (GroP) subunits to the end of the growing chain.	1.09015e-65
NZ_CP024593.1|WP_005874854.1|1096166_1097183_-|type-I-PGING-CRISPR-associated-protein-Cas7/Csp1	gnl|CDD|132528	TIGR03489, cas_csp1, CRISPR-associated protein Cas7/Csp1, subtype PGING. Members of this protein family are Csp1, a CRISPR-associated (cas) gene marker for the Pging subtype of CRISPR/cas system, as found in Porphyromonas gingivalis W83 and Bacteroides forsythus ATCC 43037. This protein belongs to the family of DevR (TIGR01875), a regulator of development in Myxococcus xanthus located in a cas gene region. A different branch of the DevR family, Cst2 (TIGR02585), is a marker for the Tneap subtype of CRISPR/cas system.	0
NZ_CP024593.1|WP_005874856.1|1099429_1100095_-|CRISPR-associated-endoribonuclease-Cas6	gnl|CDD|273848	TIGR01877, CRISPR-associated_endoribonuclease_Cas6_1, CRISPR-associated endoribonuclease Cas6. CRISPR is a term for Clustered, Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This broadly distributed, highly divergent Cas family is now characterized as an endoribonuclease that generates guide RNAs for host defense against phage and other invaders. The family contains a C-terminal motif GXGXXXXXGXG, where the each X between two Gly is hydrophobic and the spacer XXXXX contains (usually) one Arg or Lys. The seed alignment for the current version of this model has gappy columns removed. Members of this protein family are found associated with several different CRISPR/cas system subtypes, and consequently we designate this family Cas6.	2.05367e-36
NZ_CP024593.1|WP_013815288.1|1074812_1077314_+|TonB-dependent-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	1.15123e-42
NZ_CP024593.1|WP_088442951.1|1072645_1073638_-|putative-sulfate-exporter-family-transporter	gnl|CDD|225411	COG2855, COG2855, Predicted membrane protein [Function unknown].	1.65319e-53
NZ_CP024593.1|WP_005874855.1|1097193_1098693_-|type-I-PGING-CRISPR-associated-protein-Cas8c/Csp2	gnl|CDD|132526	TIGR03487, cas_csp2, CRISPR-associated protein Cas8c/Csp2, subtype PGING. Members of this protein family are cas, or CRISPR-associated, proteins. The two sequences in the alignment seed are found within cas gene clusters that are adjacent to CRISPR DNA repeats in two members of the order Bacteroidales, Porphyromonas gingivalis W83 and Bacteroides forsythus ATCC 43037. This cas protein family is unique to the Pging (Porphyromonas gingivalis) subtype.	0
NZ_CP024593.1|WP_099811787.1|1068969_1070367_-|signal-peptidase-I	gnl|CDD|182787	PRK10861, PRK10861, signal peptidase I.	5.24562e-17
NZ_CP024593.1|WP_077070303.1|1098689_1099433_-|type-I-PGING-CRISPR-associated-protein-Cas5p	gnl|CDD|132527	TIGR03488, cas_Cas5p, CRISPR-associated protein Cas5, subtype PGING. CC Members of this protein family are cas, or CRISPR-associated, proteins. The two sequences in the alignment seed are found within cas gene clusters that are adjacent to CRISPR DNA repeats in two members of the order Bacteroidales, Porphyromonas gingivalis W83 and Bacteroides forsythus ATCC 43037. This cas protein family is unique to the Pgingi (Porphyromonas gingivalis) subtype, but shows some sequence similarity to genes of the Cas5 type (see TIGR02593).	2.18286e-157
NZ_CP024593.1|WP_005874861.1|1093323_1093836_-|CRISPR-associated-protein-Cas4	gnl|CDD|366863	pfam01930, Cas_Cas4, Domain of unknown function DUF83. This domain has no known function. The domain contains three conserved cysteines at its C-terminus.	3.76681e-68
NZ_CP024593.1|WP_099811788.1|1068353_1068980_-|signal-peptidase-I	gnl|CDD|274044	TIGR02227, Inactive_signal_peptidase_IA., signal peptidase I, bacterial type. This model represents signal peptidase I from most bacteria. Eukaryotic sequences are likely organellar. Several bacteria have multiple paralogs, but these represent isozymes of signal peptidase I. Virtually all known bacteria may be presumed to A related model finds a simlar protein in many archaea and a few bacteria, as well as a microsomal (endoplasmic reticulum) protein in eukaryotes. [Protein fate, Protein and peptide secretion and trafficking].	1.3881e-12
NZ_CP024593.1|WP_005874865.1|1093855_1096177_-|CRISPR-associated-helicase/endonuclease-Cas3	gnl|CDD|273707	TIGR01587, CRISPR-associated_endonuclease/helicase_Cas3, CRISPR-associated helicase Cas3. This model represents the highly conserved core region of an alignment of Cas3, a protein found in association with CRISPR repeat elements in a broad range of bacteria and archaea. Cas3 appears to be a helicase, with regions found by pfam00270 (DEAD/DEAH box helicase) and pfam00271 (Helicase conserved C-terminal domain). Some but not all members have an N-terminal HD domain region (pfam01966) that is not included within this model.	1.86657e-160
NZ_CP024593.1|WP_143733526.1|1100136_1100406_-|DUF1661-domain-containing-protein	gnl|CDD|285160	pfam07877, DUF1661, Protein of unknown function (DUF1661). This is a family containing bacterial proteins of unknown function. Many of the proteins in this family are hypothetical.	1.11955e-05
NZ_CP024593.1|WP_010956473.1|1092047_1092311_-|CRISPR-associated-endonuclease-Cas2	gnl|CDD|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	2.04042e-30
NZ_CP024593.1|WP_043894976.1|1070382_1071099_-|4-hydroxy-tetrahydrodipicolinate-reductase	gnl|CDD|234595	PRK00048, PRK00048, dihydrodipicolinate reductase; Provisional.	4.17667e-53

Protein sequences

>NZ_CP024593.1|WP_074453431.1|1080711_1081797_-|IS5-family-transposase
MAYQSKNTDEHVTFADALLSKRYRKAQNDFLNQVDRLIDWRPIRTLINKKYTKRQNAIGAPAYDVILLFKMLLLETWYNLSDCALEERINDSITFSRFLGLKMEEVSPDHSTISRFRSALTELGLMDKLLAQFNKQLSRHHISVREGVLVDASLVETPHKPNGTITIEVADDREDNRSEEEKEAEEDYQKQVVRRRKGTDEEARWVYKQKRYHYGYKKHCPANVQGIVQKVITTAANRSDTKEFIPLLQGANIPQGTAVLADKGYACGENRSYLQTHHLQDGIMHKAQRNRALTEGEKQRNKAIGPIRSTIERTFGSIRRWFHGGRCRYRGLAKTHTQNILESIAFNLYRTPGIIMSSSLG
>NZ_CP024593.1|WP_054191584.1|1078703_1080452_+|phospho-sugar-mutase
METDKLLDQVRAKARIWLGTEYDDSSRKAVQAMLDNADTTELVDAFYRDLEFGTGGLRGIMGAGTNRMNRYTVGAATQGLSNYLLREFAGSSDISVVIGYDCRNNSRFFADTAAAVFSANGIGVYLFEELRPTPEISYAIRHLGCKSGVMITASHNPKEYNGYKAYWEDGAQIIAPHDRNIIAEVNRIRSVDEIKFEAKPELIRMIGENIDSAFIAEVKALSLSPESIARHRDMKIVYTPIHGTGSTVVPRALREYGFANIIHVPEQDVVSGDFPTVHSPNPEEPAALALAIAKAEETGADLVLASDPDADRIGVAVRNNEGRMVLINGNEICSLLIYYSIMRRKELGDLHPDDYIVKTIVTTELIRDIAKKEHVSMFDCYTGFKWIAAVIRENEGRRRYIGGGEESYGFLWEDFIRDKSSVSACALFCEMAAWALDRGMSVYRLIRSIYLEYGLYYEKGLSVVRKGKSGAEEIEAMMRNYREYAPVELGGSPVQEILDYASLEGKDFTRGEKFSLDMPTTSNVLQYKTEDGTKVSIRPSGTEPKIKFYIGVHFSVANEQELDRAYIVAEEKIATILHDLGV
>NZ_CP024593.1|WP_054191585.1|1077893_1078631_+|DNA-repair-protein-RecO
MIIVSRAIVLHNTAYNDSYSIAHLFSRESGRVSYLIPRSSKRGKSGGSLRLLISPLNELEITAEHKQHRDLHFIKEAKLCSLHGRIQSDPVRNSIALFLAEFLYLILRLPEADTNLYDFVAFSIDKLEEMDGPMANFHLAFLFRLLVPLGLIPDLQFGGSVIPRWFDPADGRFVPNAPAHGRGIPPHQSTYLQLFSRITFDNMKAFRLSRGERRQVLDYLVDYYRFHLPPFPLLKTPDILSTLFY
>NZ_CP024593.1|WP_013815288.1|1074812_1077314_+|TonB-dependent-receptor
MKQLNIISFIIAFLFLGTSASAQQSGGSVTGTVVDKSSKEPIAYVQVFVKGTTLGTSTDANGNYSIKGIPSGNQTIVARLMGYSTCEEKVHIEKGGSRHVDLYLTEEILSLDGVVVSANRNETFRRQAPSLVTVLSPELFLKTNSTNLSQGLKFQPGLRVEDNCQNCGFNQVRINGLEGAYSQILIDSHPIFSSLAGVYGLEQMPANMIERVEVIRGGGSALFGSNAVGGVINVITKEPLRNSAEISHSTMTFDHAKGWGSFQNTTQFNGSMLTEDRKAGVMVFGQHNYRPGQDIDGDSFTELPNLRNRSLGFRSYYKTGLYSKATLEYHSMQEYRRGGDRLDNPPFEAQIAEYLQHYINGGSFKFDQGFSGGKDFFSLYASAQDVQRRSYYGGGDYTENLLNGAVQSGSTESDEYNNAFTALTSYGTTKGFDLQGGGMYRHTFGENWDFTGGLEYIYGQLDDRSGYRPSKIDQNTSTFSQYDQLEYKTEKLSALIGARIDYVLLNQDGKRYIDPLFIFSPRANVRYNPNKNLSFRLSYSEGFRAPQYFDEDLHVELAGGTPISRVLSPNLKEERSRSISASFDYYHRADEWQFNIMGEAFSTFISNQFKPSDKVETTSDGKEWIIRTIYNDKDGVSKVYGVNLEGRIAYNKSFDLQLGGTWQRSRYGSIYTAVEADKTTGQAEISVKDYVRTPNLYGYFVATVRPTEHFAINLSGTFTGKMDVVHEAYEGDIPAEHIAPDGSFDFEMNGQQFKGLAEGHAKLVKTPAFADIDLKLSHDFHLASTMTLELNAGIQNIFNSYQKDTDKGPGRASTYVYGPMQPRRIFVGTKINF
>NZ_CP024593.1|WP_099811786.1|1074146_1074506_+|hypothetical-protein
MKERLNQTVRYFLPILFAVYAGLVISFTHVHIINGVIIVHSHVQWGDNESNPQDNPHSDSELILYNQLSTIFTTYLDTPAIDLKEPVRVVGVVPFFCDNLIALISELTPSNHLRAPPVA
>NZ_CP024593.1|WP_088442951.1|1072645_1073638_-|putative-sulfate-exporter-family-transporter
MNTDNPKSHISRIAYPAIIVFLILTLLGSLVERFHSFTSWLTPPVALLMGLAYALIFGSTHRRANKLGSKVLLQYSVVGLGFGMNLGESLASGRDGMMFTIISVFGTLLLGWFIGRKILQMNRNTSALISAGTAICGGSAIAAVGPILKAEEHEMSVALGTVFLLNAVALFIFPSIGHWLALDQQQFGTWAAIAIHDTSSVVGAGSAYGEEALRVATTIKLTRALWIVPLTLVFSFVYKTKGAKRFPVPLFILFFIGAIILNTYLLEAYFPEVGRFVASLARKGLTLSLFFIGASLTKEVIASVGVRALLQGLFLWILISVGSLAFILLI
>NZ_CP024593.1|WP_081003114.1|1071158_1072502_-|deoxyguanosinetriphosphate-triphosphohydrolase-family-protein
MTMMQWERLLSDKRVGMEHYHQPKQSAQPWERTDFERDYDRMVFSSPFRRLQNKAQVFPLAGNIFVHNRLTHSLEVSCVGRSLGNNITRGLKARYGELPWESGAISAIVSAACLAHDMGNPPFGHSGERAISAYFREGKGRVWEDAVRKEGGRWEDFLHFEGNANAFRLLTHQFEGRRKGGFALTYSTVASIVKYPYSSEMAGKAGKFGFFATEEDTFLMIAEELGMLCRNEHPVKYARYPLVYLVEAADDICYQIMDIEDAYKLRILTYAETENLFLAFCPEEELGHMRGVLDHITDANEQIAYLRSRVISLLVESCTRVFLDHEDEILSGTFSGTLIGAMEPRLKEAYGACARMAYSKIYVARDVVDVELAGHQIFGALIDKMMQALTNPDHAYSRTLLSRVSTQYNIREESLYGKIQCTLDYISGMTDIYALDLYRKITGMNLR
>NZ_CP024593.1|WP_043894976.1|1070382_1071099_-|4-hydroxy-tetrahydrodipicolinate-reductase
MKIVLIGYGKMGHVIERIACSRGHEVVLTIDAGEEDRFDSIAFRSADVAIEFTRPDAAYANCSRCMDKSVPVVCGTTGWTEHLPELEERCRREGKTLFWASNFSIGVNLFFSLSRMFARLMSRHDQYRPHLTEIHHVHKLDAPSGTAITLAEGLIAESPSLDAWRLTETPEENELPITSIREGEVPGTHSISYTSEVDRLTICHEAFGREGFALGAVLAAEYAATHKGFLTMNDLISL
>NZ_CP024593.1|WP_099811787.1|1068969_1070367_-|signal-peptidase-I
MTFHWKDLTPWRRIKGVAITILYLFFCIWAGPFWLIFLPLIVDYYFFHIIKWGWYKNIRNKTLRIICSWVADIIYCVVAVTFIFAFLFQNFAIPTSSLEKTLLIGDYLFVSKLSYGPRSPMTPLGVPLTHNTMPLTGGKSFSDKPLLPYKRLKGFGHVKEGDLVVFNFPAGDTVAVKQPNPDYYMWKKLVGREELWSNPDFYGEIVYRPVDRRDHYVKRCVGMPGQELSIRNNQIYIDGKEQRNPRNMQLNYLVRMSREMSVDLIDELGISYDDVRAASSEELKASVVSNLIDSASNQPQIIYHLPLTQGMLDKLQAEPSFVKAVEEPTPIGPLYPLEYETGWTRDNYGPIVIPAKGMTVRLTPLNLALYSRCIRNFEGNKLVQKADGTVLINGRPADSYTFKMDYYFMMGDNRHNSADSRYWGFVPEDHIVGKPVFIWLSLNKDKSLFGGKIRFGRMMRTVNAD
>NZ_CP024593.1|WP_099811788.1|1068353_1068980_-|signal-peptidase-I
MQIKSRYKNRIFFIGLPAVVLLSAVLIRLFLVTTYRVRSDAMLPTYRSGKLLWINRIASPDRGDVLVIKYRQDGEANSRFYLARLIGLPGDTLFLSKGGVVANRQKLKLPTSLLPREPYKIIVPRNDRTYRLTPLSLLAYRRAIEEECSSNISFRRGKLYRDGAETAFSHFRRNYYWILADNPASGPDSRHLGIVPEESIVGVVMNAN
>NZ_CP024593.1|WP_010956473.1|1092047_1092311_-|CRISPR-associated-endonuclease-Cas2
MYIILVYDIGEKRVGKMLKLCRKYLNWIQNSVFEGEISEVKLLELKSRAAGIMEKEEDSLIIFSSRQERWLEKEIIGKERSATDIFL
>NZ_CP024593.1|WP_005874853.1|1092310_1093327_-|type-I-B-CRISPR-associated-endonuclease-Cas1
MKKTYYLFNPGELSRKDNTIRFVPIQEGENGQEQAGQARYIPVEGISDFYVFGSLRANSSLYNFLGSNDIAVHFFDYYENYTGSFMPRDFLLSGKMLLAQASAYKNKKKRLFLARKFIEGAASNMQKNLAYYNNRGKDMQPMMELIDKYSLRLKETTTIEALMGIEGNIRQAYYDAFNLIIDPFEMGVRSKQPPQNEVNALISFGNMMCYTLCLKAIHQSQLNPTISFLHTPGERRYSLCLDISEVFKPILVDRTIFKVMNKRIIQAKHFDKQLNKCILNPSGKKLFVQAFEERLSETIRHRKLNRSVSFRHLVKLECYKIAKDILGIEEYQPFKMYW
>NZ_CP024593.1|WP_005874861.1|1093323_1093836_-|CRISPR-associated-protein-Cas4
MNTISGTHFNYHQVCRRKLWLFSAGITMEHTSDLVYEGKLIHETTYQQRPERYQELELDGIKIDFYDAKNRVVHEVKKSNKISPAHRLQLLYYLYVLERNGVLGATGILEYPTLRKKEEVILSDIDRERIREIEQEILQIISHEDCPPVIDSGICKNCSYYEFCFSGEEQ
>NZ_CP024593.1|WP_005874865.1|1093855_1096177_-|CRISPR-associated-helicase/endonuclease-Cas3
MINKESPILAKPSGITLDVHAENVIQEGALLLKGLGCTKEKYFQTTAKQIVQRVELACKYHDIGKRNKIWQDACKKDYKAYLIWKKIHPNKSFEDYTIECREEAGKFLRQTHVRHEFYSIKGLLNNNPPPNNNPPYWLKIAIAAHHRKLSMKHEERWLSSDEDICSVWKDIRRLSNYFFDDRNSVLSDIAIKQYEFAGPRSLLQLADHRASAKEESKCIPDPIAFSYTFPEKWEKRPVQKLVEKHWRDELLLVRAPTGAGKTDAALLWASHQIKHRKADRLIIAMPTRFTTNALALSVSSTLSSTGLYHSSAWTQNFSSKIDNGEIALEQARYYHNQARLLQTPITVCTIDHLLSSLTLCDEEHQTITFALANACLVIDEADFYDQFTQANILVLLEVLKYWKVPILLMSASLPDNIVQEYRKIGYDIKHILEDTSDIERARFSLIEKRDVSEISQMQDLLQLCLDRGSAIIFANTVDRAQAYYQWFLENGHEEEVILYHSRYTETDKIEKEAQLLLRLGRSAWDNDRANGVAILTQIGEMSVNISADIMISDLCPIDRLTQRCGRLCRFSRKIGDLYIIRPMREGNLFPAPYYQNVGPSQKLEPNDALIQTDELLEKGMYSAANLVQLLNKVYANQTVFSTEASRNADRLREMFKANWLINPIEYLDEEIGSTNFWRARNIMPRCRIYIKRPLQSFRNYSDFRRWETDVAIDIPIYVIKKAMRMSDTVCSQVKVCIGKNDYTLIVINAKCYNNVRGLFFSESVLEEPNFEFL
>NZ_CP024593.1|WP_005874854.1|1096166_1097183_-|type-I-PGING-CRISPR-associated-protein-Cas7/Csp1
METKKIAGVLVTMVAPFENHMANGGEKLFGNASSIKRRPDGRVYVSGQMQRHVLFSAIDRLNHLDKAKGTTFVSNGDGITNLIEIDLRADLGGFMHTNKGDYSDRRIAPLSVTPATALDTSSVGRDLLVRIRFDKSSDAKNQALATREYSEQDKMNMNFFLDITSVGVSKSFVYKDGLNLGTKYFKHITDDEKKRRVKLFLEATRIMNDYANQARNAVCGEPEKVLIVFDDRLSRKACRYYTVGEKEQANIIKELDQYQVKYFVGDDASDYSVADAYRDAMNYLDKATLVDFAEGEEIMTFAEAFECKEKEPQEKKSKKGKDKATSAQNLFAEQQDDQ
>NZ_CP024593.1|WP_005874855.1|1097193_1098693_-|type-I-PGING-CRISPR-associated-protein-Cas8c/Csp2
MNTNHYYIRYGCAITLYDNHVSERERLTPKELRFSIEKAVSSFRIQAQEPFSPGSKARFSFVKRKDGNTKNGIFLSPHIVTKDMHAQKVWTKASKFLEIDYLGKDNEREGLLKKDNVSMSNIPISGEYLTFGEKDTGRGSAKISVEEQTYGLITTLTPLKPALQVGKDNFCIIPDIPLNQMVDFIALFDKMQITHLSGEAMLGNIDNKGIPHRPKIFRGNFPNSPKSDRMGAIALLGAIGEFAKHAEFSTLAQKVLDSLKGSTLYLITYGNAIPFTFHHYIIDLAKEGKLHSIVDSLFYSRLYKKEKRVYGDTDYDRFDFFTNRFLQSFNKAAFDDFFSSRVEYPNQIKILFQMFFTKMEKLKTDVIASAQILGSWLNQVAYFAAKEEADSRISPGNIFEEKAKFLVMMESSIYAAKRGDALIAQILILAGRLSKNEAPKEALLFMEKTITGEIDLSVAKNLLIAYMRIRREEKQRDLNSVKNDDAIPSDINIDDLTNT
>NZ_CP024593.1|WP_077070303.1|1098689_1099433_-|type-I-PGING-CRISPR-associated-protein-Cas5p
MKYNMKNIDLSILGKDPDLSASIKLHIEPHAPISMVSELPGSYYKALLYPDKHILCGLFENVLGWHFSRKDREIITKEIKNIRKKTKKGYIPPTIRSIFIPLLSDFFELDSVRIVSTDSPFFYNDLWKRAFRRKDAGKIHFGGTQNIDYTLVMDKFRFMCENERALETEEKTDQKEEKFLRENIDRISFFYTTPTNREYLFFEGNYECVIKMDPQLVDLLSKTLPQQNMGYLGNSEGWVTLYLEEKS
>NZ_CP024593.1|WP_005874856.1|1099429_1100095_-|CRISPR-associated-endoribonuclease-Cas6
MRIELSIKADDSLVSFSHQHLLVGTLQKWLGENDMHGKSISYSFSRLNGGKLVSELNSILFADWANMFVSAHDPELIRRMLAGIRQDPEMFKSLCVREVTVIEDPDMTDREIFFPASPILLKRWREDNGFDHIVYTDEAANALLTENLRKKLQAVGIDDPTATASFVPDQGKAKVMLIDYRGVKNKASWCPIRIIGNAETKLFAWNAGIGNSTGIGFGAIK
>NZ_CP024593.1|WP_143733526.1|1100136_1100406_-|DUF1661-domain-containing-protein
MRPRKTWRVNFFVLVREIKNSRATTKNFLFRFFRKHAPQSEHFRFVFYTPPSPLFYFQCGFRKIPRNDGCYISDFLANKHKKIRINYSF
>NZ_CP024593.1|WP_099811782.1|1100742_1102674_-|LTA-synthase-family-protein
MKTLFERGELLFRKRSGFCYVIGVFVLFLLYFLFQKVIFLLVYSGQLAGIGTSSRDIAAIFLHGLRHDAAVAAYLTVLPLLFAGINAIAGWGEKKIGRILRQILKHYYTLISFFVGLIYTADLMLFGYWGFRLDATPLFYLRQPQEAMASATAPQLLIGLLITVVFVCIPAFVLHRFHRRYFPTKVAAHPHIAGIWKPVVGGAFLFLLIRGGVGVATLNVGSVFHSPKQLHNQAAVNPVFSFLYTCMHSEEDYSNYQFLSEEDCIKAFEQLRLYGCSDGSEVRESASDSTERILSTDRPNIVLILLESFSANAVGCLGGTPGHTPCIDSLAQNGILFSQAFASSFRTDRGTVATLSGYPSQPNSSIIKYPNKVRNLPGIAASLRTVGYSTHHLYGGDADFTNVRSYLYATGYDEVTDVSSFPIKTRLSKWGTPDHISFPRLLDDCRRLEKEKKPYFYSFLTLSSHEPFDVPSLHHPDPYLNSVFYTDSCFGDYVRSMQQSPEWKNTLIIAVSDHGYPYPTDQAMPDQPGRYGIVMLWTGGAILRPIRFEEVVSQSDLPATLLAQLGLTHDEFVFSKDVFRSSSPHFAYFSFPGLVGLATSEGTTIYDFAGDKIVYGHEAPLADQRAIAAKVMLQSVMKDMLSR

Crispr_ID: NZ_CP024593_7

• CRISPR_ID: NZ_CP024593_7
• CRISPR_location: 1143431-1143526
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP024593_7

Consensus_repeat	Method
GTAATGGTCGTAGAGTCTAGGAGCTTGACG	CRISPRCasFinder

spacers of NZ_CP024593_7

>7.1|1143461|36|NZ_CP024593|CRISPRCasFinder
AAGGGTGGCGACCAATTTTTCCATCATGCAAACGTT

CRISPR arrays and Neighbor proteins around NZ_CP024593_7

CRISPR arrays

The CRISPR arrays of NZ_CP024593_7

>merge|NZ_CP024593|7|1143431-1143526|CRISPRCasFinder
GTAATGGTCGTAGAGTCTAGGAGCTTGACGAAGGGTGGCGACCAATTTTTCCATCATGCAAACGTTGTAATGGTCGTAGAGTCTAGGAGCTTGACG

>NZ_CP024593|7|8|1143431-1143526|CRISPRCasFinder
GTAATGGTCGTAGAGTCTAGGAGCTTGACG	AAGGGTGGCGACCAATTTTTCCATCATGCAAACGTT
GTAATGGTCGTAGAGTCTAGGAGCTTGACG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024593.1|WP_099896732.1|1152204_1157928_+|alpha-2-macroglobulin	unknown	unknown	gnl|CDD|380081
NZ_CP024593.1|WP_004583703.1|1136968_1137244_-|hypothetical-protein	unknown	unknown	gnl|CDD|378938
NZ_CP024593.1|WP_004585605.1|1150615_1151293_-|peptide-deformylase	unknown	unknown	gnl|CDD|234668
NZ_CP024593.1|WP_077070291.1|1138393_1139047_+|ATP-dependent-dethiobiotin-synthetase-BioD	unknown	unknown	gnl|CDD|234625
NZ_CP024593.1|WP_004585610.1|1159021_1160638_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|237894
NZ_CP024593.1|WP_004583702.1|1136335_1136713_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_099810608.1|1145435_1146317_+|peptidase	unknown	unknown	unknown
NZ_CP024593.1|WP_099811770.1|1133566_1135852_-|AAA-family-ATPase	unknown	unknown	gnl|CDD|350795
NZ_CP024593.1|WP_004583708.1|1139910_1140891_-|dihydroorotate-dehydrogenase-like-protein	unknown	unknown	gnl|CDD|236051
NZ_CP024593.1|WP_021664146.1|1131189_1131945_+|zinc-ribbon-domain-protein	unknown	unknown	gnl|CDD|224495
NZ_CP024593.1|WP_099810610.1|1146558_1148496_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|223562
NZ_CP024593.1|WP_005874417.1|1135942_1136323_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_004585606.1|1151289_1151742_-|Holliday-junction-resolvase-RuvX	unknown	unknown	gnl|CDD|340815
NZ_CP024593.1|WP_099896731.1|1139149_1139845_-|OmpA-family-protein	unknown	unknown	gnl|CDD|143586
NZ_CP024593.1|WP_005874285.1|1148492_1150580_-|tetratricopeptide-repeat-protein	unknown	unknown	gnl|CDD|274350
NZ_CP024593.1|WP_157763375.1|1151859_1152003_+|DUF1661-domain-containing-protein	unknown	unknown	gnl|CDD|285160
NZ_CP024593.1|WP_053444622.1|1144429_1145227_+|M48-family-metallopeptidase	unknown	unknown	gnl|CDD|320690
NZ_CP024593.1|WP_054190921.1|1137471_1138365_+|4-hydroxy-tetrahydrodipicolinate-synthase	unknown	unknown	gnl|CDD|235107
NZ_CP024593.1|WP_099810615.1|1157941_1158886_+|2-dehydropantoate-2-reductase	unknown	unknown	gnl|CDD|273247
NZ_CP024593.1|WP_099811771.1|1132207_1133572_+|tRNA-lysidine(34)-synthetase-TilS	unknown	unknown	gnl|CDD|238950

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP024593.1|WP_099896732.1|1152204_1157928_+|alpha-2-macroglobulin	gnl|CDD|380081	pfam17973, bMG10, Bacterial Alpha-2-macroglobulin MG10 domain. Alpha-2-macroglobulins (A2Ms) are plasma proteins that trap and inhibit a broad range of proteases and are major components of the eukaryotic innate immune system. However, A2M-like proteins were identified in pathogenically invasive bacteria and species that colonize higher eukaryotes. Bacterial A2Ms are located in the periplasm where they are believed to provide protection to the cell by trapping external proteases through a covalent interaction with an activated thioester. This domain is found on the C-terminal region in A2Ms in bacteria. Structure analysis of Salmonella enterica ser A2Ms (SA-A2Ms) show that they are composed of 13 domains, all of which fold as variants of beta sandwiches with the exception of the TED, which consists of 14 alpha helices. Most of the beta sandwich domains appear to serve a structural role and are referred to as the macroglobulin-like (MG) domains. This is the MG10 domain. MG10 is markedly different from the other MG domains in that it has more beta strands and an alpha helix. The position of MG10 is stabilized by, in addition to other hydrogen bonds, the formation of a beta sheet with MG9.	2.1001e-29
NZ_CP024593.1|WP_004583703.1|1136968_1137244_-|hypothetical-protein	gnl|CDD|378938	pfam12732, YtxH, YtxH-like protein. This family of proteins is found in bacteria. Proteins in this family are typically between 100 and 143 amino acids in length. The N-terminal region is the most conserved. Proteins is this family are functionally uncharacterized.	2.30217e-10
NZ_CP024593.1|WP_004585605.1|1150615_1151293_-|peptide-deformylase	gnl|CDD|234668	PRK00150, def, peptide deformylase; Reviewed.	1.0936e-76
NZ_CP024593.1|WP_077070291.1|1138393_1139047_+|ATP-dependent-dethiobiotin-synthetase-BioD	gnl|CDD|234625	PRK00090, bioD, ATP-dependent dethiobiotin synthetase BioD.	8.66705e-84
NZ_CP024593.1|WP_004585610.1|1159021_1160638_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein	gnl|CDD|237894	PRK15064, PRK15064, ABC transporter ATP-binding protein; Provisional.	0
NZ_CP024593.1|WP_099811770.1|1133566_1135852_-|AAA-family-ATPase	gnl|CDD|350795	cd18037, DEXSc_Pif1_like, DEAD-box helicase domain of Pif1. Pif1 and other members of this family are RecD-like helicases involved in maintaining genome stability through unwinding double-stranded DNAs (dsDNAs), DNA/RNA hybrids, and G quadruplex (G4) structures. The members of Pif1 helicase subfamily studied so far all appear to contribute to telomere maintenance. Pif1 is a member of the DEAD-like helicases superfamily, a diverse family of proteins involved in ATP-dependent RNA or DNA unwinding. This domain contains the ATP-binding region.	2.48783e-46
NZ_CP024593.1|WP_004583708.1|1139910_1140891_-|dihydroorotate-dehydrogenase-like-protein	gnl|CDD|236051	PRK07565, PRK07565, dihydroorotate dehydrogenase-like protein.	3.05191e-160
NZ_CP024593.1|WP_021664146.1|1131189_1131945_+|zinc-ribbon-domain-protein	gnl|CDD|224495	COG1579, COG1579, Zn-ribbon protein, possibly nucleic acid-binding [General function prediction only].	2.25726e-17
NZ_CP024593.1|WP_099810610.1|1146558_1148496_-|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].	0
NZ_CP024593.1|WP_004585606.1|1151289_1151742_-|Holliday-junction-resolvase-RuvX	gnl|CDD|340815	cd16964, YqgF, putative pre-16S rRNA nuclease YqgF and RuvX family. Escherichia coli YqgF has been shown to act as a pre-16S rRNA nuclease, presumably as a monomer. It is involved in the processing of pre-16S rRNA during ribosome maturation. The RuvX gene product from Mycobacterium tuberculosis was shown to act, in a dimeric form, as a Holliday junction resolvase (HJR). HJRs endonucleases specifically resolve Holliday junction DNA intermediates during homologous recombination. Holliday junctions are formed by the reciprocal exchange of strands between two DNA duplexes. HJRs occur in archaea, bacteria, and in the mitochondria of certain fungi; they may form homodimers and display structural similarity to RNase H and Hsp70.	6.47574e-49
NZ_CP024593.1|WP_099896731.1|1139149_1139845_-|OmpA-family-protein	gnl|CDD|143586	cd07185, OmpA_C-like, Peptidoglycan binding domains similar to the C-terminal domain of outer-membrane protein OmpA. OmpA-like domains (named after the C-terminal domain of Escherichia coli OmpA protein) have been shown to non-covalently associate with peptidoglycan, a network of glycan chains composed of disaccharides, which are crosslinked via short peptide bridges. Well-studied members of this family include the Escherichia coli outer membrane protein OmpA, the Escherichia coli lipoprotein PAL, Neisseria meningitdis RmpM, which interact with the outer membrane, as well as the Escherichia coli motor protein MotB, and the Vibrio flagellar motor proteins PomB and MotY, which interact with the inner membrane.	8.9625e-42
NZ_CP024593.1|WP_005874285.1|1148492_1150580_-|tetratricopeptide-repeat-protein	gnl|CDD|274350	TIGR02917, TPR_domain_protein, putative PEP-CTERM system TPR-repeat lipoprotein. This protein family occurs in strictly within a subset of Gram-negative bacterial species with the proposed PEP-CTERM/exosortase system, analogous to the LPXTG/sortase system common in Gram-positive bacteria. This protein occurs in a species if and only if a transmembrane histidine kinase (TIGR02916) and a DNA-binding response regulator (TIGR02915) also occur. The present of tetratricopeptide repeats (TPR) suggests protein-protein interaction, possibly for the regulation of PEP-CTERM protein expression, since many PEP-CTERM proteins in these genomes are preceded by a proposed DNA binding site for the response regulator.	1.89871e-17
NZ_CP024593.1|WP_157763375.1|1151859_1152003_+|DUF1661-domain-containing-protein	gnl|CDD|285160	pfam07877, DUF1661, Protein of unknown function (DUF1661). This is a family containing bacterial proteins of unknown function. Many of the proteins in this family are hypothetical.	0.00770721
NZ_CP024593.1|WP_053444622.1|1144429_1145227_+|M48-family-metallopeptidase	gnl|CDD|320690	cd07331, M48C_Oma1_like, Peptidase M48C, integral membrane endopeptidase. This subfamily contains peptidase M48C Oma1 (also called mitochondrial metalloendopeptidase OMA1) protease homologs that are mostly uncharacterized. Oma1 is part of the quality control system in the inner membrane of mitochondria, with its catalytic site facing the matrix space. It cleaves and thereby promotes the turnover of mistranslated or misfolded membrane proteins. Oma1 can cleave the misfolded multi-pass membrane protein Oxa1, thus exerting a function similar to the ATP-dependent m-AAA protease for quality control of inner membrane proteins; it cleaves a misfolded polytopic membrane protein at multiple sites. It has been proposed that in the absence of m-AAA protease, proteolysis of Oxa1 is mediated by Oma1 in an ATP-independent manner. Oma1 is part of highly conserved mitochondrial metallopeptidases, with homologs present in higher eukaryotes, eubacteria and archaebacteria, all containing the zinc binding motif (HEXXH). It forms a high molecular mass complex in the inner membrane, possibly a homo-hexamer.	2.06945e-90
NZ_CP024593.1|WP_054190921.1|1137471_1138365_+|4-hydroxy-tetrahydrodipicolinate-synthase	gnl|CDD|235107	PRK03170, PRK03170, dihydrodipicolinate synthase; Provisional.	1.54714e-135
NZ_CP024593.1|WP_099810615.1|1157941_1158886_+|2-dehydropantoate-2-reductase	gnl|CDD|273247	TIGR00745, Putative_2-dehydropantoate_2-reductase, 2-dehydropantoate 2-reductase. This model describes enzymes that perform as 2-dehydropantoate 2-reductase, one of four enzymes required for the de novo biosynthesis of pantothenate (vitamin B5) from Asp and 2-oxoisovalerate. Although few members of the seed alignment are characterized experimentally, nearly all from complete genomes are found in a genome-wide (but not local) context of all three other pantothenate-biosynthetic enzymes (TIGR00222, TIGR00018, TIGR00223). The gene encoding this enzyme is designated apbA in Salmonella typhimurium and panE in Escherichia coli; this protein functions as a monomer and functions in the alternative pyrimidine biosynthetic, or APB, pathway, used to synthesize the pyrimidine moiety of thiamine. Note, synthesis of the pyrimidine moiety of thiamine occurs either via the first five steps in de novo purine biosynthesis, which uses the pur gene products, or through the APB pathway. Note that this family includes both NADH and NADPH-dependent enzymes, and enzymes with broad specificity, such as a D-mandelate dehydrogease that is also a 2-dehydropantoate 2-reductase. [Biosynthesis of cofactors, prosthetic groups, and carriers, Pantothenate and coenzyme A].	1.38652e-97
NZ_CP024593.1|WP_099811771.1|1132207_1133572_+|tRNA-lysidine(34)-synthetase-TilS	gnl|CDD|238950	cd01992, PP-ATPase, N-terminal domain of predicted ATPase of the PP-loop faimly implicated in cell cycle control [Cell division and chromosome partitioning]. This is a subfamily of Adenine nucleotide alpha hydrolases superfamily.Adeninosine nucleotide alpha hydrolases superfamily includes N type ATP PPases and ATP sulphurylases. It forms a apha/beta/apha fold which binds to Adenosine group. This domain has a strongly conserved motif SGGXD at the N terminus.	5.04871e-69

Protein sequences

>NZ_CP024593.1|WP_004583708.1|1139910_1140891_-|dihydroorotate-dehydrogenase-like-protein
MIDLSTEFAGLRLKNPIVAASSGLTRNLKTIKDLEAAGVAAIVLKSLFEEQIEAEMSQMMSPMDYPEAADYINAYVQSNEISKHLDFLREVKREVAIPVIASINCFRSDSWVDFAKQFEEAGADALEINVMRLNTDLFFDANKAEQMYVDIISSLIKAIRIPVVVKLSKSFANIPSLVDKLRAAGAKGVVLFNRSYQPDIDIDKVQMVAGDVFTSAGEISDTIRHAGIVSALVPGISIASSTGIHDGEAALKCLLAGAHVTQICTVLYKKGPQFVAEMIATIESWMQVKGYYSVSEFRGKLNAASVKSATMYERMQFMKYFANKDN
>NZ_CP024593.1|WP_099896731.1|1139149_1139845_-|OmpA-family-protein
MKKSSVVASVLAVALVFAGCGLNNMAKGGLIGAGVGGAIGAGVGGAIGAGVGNVAGNTAVGAIVGTAVGGAAGALIGKKMDKQKKELEAAVPDATIQTVNDGEAILVTFDSGILFATNSSTLSSNSRTALTKFAANMNKNPDTDIRIVGHTDNTGSDKINDPLSERRAASVYSFLNSQGVSMSRMAAEGRGSHEPVADNSTAAGRSANRRVEVYILPNAKMIEQAQQGTLK
>NZ_CP024593.1|WP_077070291.1|1138393_1139047_+|ATP-dependent-dethiobiotin-synthetase-BioD
MPIIPSKVLFVTGIDTNIGKTYATAFLFDKLSESGQKVITQKLVQTGCVGASEDIEAHRRLTGYPTMEEDGLGLTCPYIFSYPASPHFAAEIDDKRVDCRIIDQATETLLSRGYDRVLLEGAGGLMVPITKDYLTADFIADRDYPIALVTSGRLGSINHTLLNLELCRHRGIPVESIVYNLYPAEDDRIIANTLDYLRFYLHKYHPDTQLMVMPERN
>NZ_CP024593.1|WP_054190921.1|1137471_1138365_+|4-hydroxy-tetrahydrodipicolinate-synthase
MDRAQLRGMGVALITPFDEKGEVDHESLRLLADYQVAGGADYIVVLGTTGESPTIEEAERSAILQTVREAVAGRCPIIVGAGGNYTERLVNRIQAMDKTGVDAILSVAPYYNKPTQEGIYRHYRTLAESTDTPIILYNVPGRTGVNIKSETTLRLATDCPNIIGIKEASGNVDQVRAIMLEKPDPFIVLSGDDHLSLSFIKEGAEGVISVIGNAYPELFSRLIHLCLENRFEEAETIQQRLEGMYYLMFVDGNPAGIKELLYQKGLIRHNILRLPLVSASDSTSTLIARVRNQIEQR
>NZ_CP024593.1|WP_004583703.1|1136968_1137244_-|hypothetical-protein
MSSQGKFSLGLLVGLAIGAAAAYFADREKRTRFVEDINSTADKVKDSVVEGYYEAKNRYQKYRRKMKGITEDMVEEIGDKYDEVLDDLRSE
>NZ_CP024593.1|WP_004583702.1|1136335_1136713_-|hypothetical-protein
MLKRLIEDIYSYLTLRTESIAYTIAEEGARLIAKLALLAMSVLMSFLILIFLSIALGFGFGRWLGIGATGGFFVVVGIYLLFFLIGYLCRHLIRRYILGRLAGEVLEIVARHQRKKEEDEEPTNK
>NZ_CP024593.1|WP_005874417.1|1135942_1136323_-|hypothetical-protein
MSRKPIIEIDMRAYYELKRRRDACDKEAERYQKDIFRCLDHVRNNYGDMIFEEVETHLIYPGSLGNKILRFLIGKKQISSSKLMTPTGRPTLHLIEQLTDFGRPLLISALLGFVKRSIVRRFRRRR
>NZ_CP024593.1|WP_099811770.1|1133566_1135852_-|AAA-family-ATPase
MNTKEYVLDFINRTNCNLFLTGNAGTGKTTLLRHIVQHTFKNCIVAAPTGIAALNAGGMTLHSLLQLPPGTFIPYEVSLESAMGVNFLTPTSFWKQTRMHASKRKLLRNMELLIIDEVSMLRADTLDLIDFVLRRVRSNPRSFGGVQVLFIGDLMQLPPVVKPHEWELMSAIYQGVFFFHSMVIRQHPPVFLELETIYRQTDVRFTSLLNNLRHNRLPADDLTYLKDHVNPTFDSTCHEGYITLTTHNHKADQINRRALEALPALPHSYQAIIKGDFPEHLYPLEPTMTLKEGARVMFVRNDTRQPRRYYNGKIAVVHSLSPSSVVVRTDGGELIEVEPHEWTNVRYSVNPETNAPEQEVIGSFRLFPLRAAWAITVHKSQGLTFEHAAIDLEGVFVPGQAYVALSRMTGPEGMILLSPPDLRGLETPQELVEYAQTKPDEKELRTSLQENSLIYWKQQSDEAFDWQSLMNIWHKHSLSYREESELSSKSHYSDRAAEQSAKIDAITEVAGRFRRQLAGLWGQSPLGFGAVKERIDKAVDYFLPQLSAIAGELSSTIQEVGKLKKAKQFAKELHELQDNLHTAVYRLLRLRAVFGALSAGQSLSRQELRTEELMTEWVRSVSPKDEALPTAAGNRKSKEKKAKEKKKTTHETTLELLLAGMSIEEVATERKLSPSTIEGHLALLIEKGRLAPDAYIDAGIVSELHPYFTNPSRIFELKSLYERLNGQYSYTLLRLYRAYFILMDAKEKGSRAREKAIEQAL
>NZ_CP024593.1|WP_099811771.1|1132207_1133572_+|tRNA-lysidine(34)-synthetase-TilS
MKISLTNRVRTTIRERKLFREGDRLVLVALSGGADSVALLCVLRELGYETVAAHCNFHLRGVESDEDAAFVEGLCRDLDVPLHRIDFDTVRYARERSISIEMAARELRYEWFGQLRKELAIEYVAVAHHADDNAETMVLNLCRGTGISGLCGMPYKRNDGIVRPLLDATRDEIEAYLLDQKITYRTDSSNEDTRFRRNLVRHRIMPLLKELNPSLQEALLRTRENLEGVAAFYSKATEDFHNTLRATSSISIREVKETPAPFTLLYDLLHPYGFNRDQIREVATSLDNPPGASFFSSSHRLLRERDRLTVLPLSPKMEVPELFGLKIGDSFLDLPDGKQLSWQRGTPADLDLEGLRLPNTKLLLPLAFVESLQEELGVRRPQRGDHIHPYGMKGCKTVSRFFIDRHVPRSRREEAWLLCQGTEVVWIMGYAADRRFAIDELSDTEEYLLFSFEL
>NZ_CP024593.1|WP_021664146.1|1131189_1131945_+|zinc-ribbon-domain-protein
MAKEKIIVENEQSVEEKLAALSKLQNTLSEIDKIKTLRGELPLEVQDLEDEIAGMQTRLENFTAGSKQLNQAVTTEKEKISTAKTLLEKYKKQLDEVRNNREFDNLSKEIEFQELEIQLSEKKIKEYNAEIQQRKTDIATLKEVLEEHSEVLAEKRGELDTIIAETKQEEEKLREKAKKLEAKIEPRLLTAFKRIRKAAHNGLAVVPVERDACGGCFNKIPPQKQLDVKLRKKIIVCEYCGRIMVDPEMGA
>NZ_CP024593.1|WP_053444622.1|1144429_1145227_+|M48-family-metallopeptidase
MKIMNVILASVLVVLLAGCSTVPISGRSQIMLVQDSEILSSSALQYKQFLSKVKISKNATSTAQVRRVGQKVAAATMLYLKQNGLGDMASQMKWEFNVVEDKAVNAFCMPGGKIVVYTGLLKLVGSDAELATVISHEVSHAVARHSNERISQEYLRQMGGNILGAAVSNKSAALQTVIGQAYGIGSQVLITLPYNRKQEYEADKIGLVFMAMAGYNPNAAITFWQKMAAQGNGQVEFLSTHPSDANRIAAIRQYMPEAMKYYKSK
>NZ_CP024593.1|WP_099810608.1|1145435_1146317_+|peptidase
MKQNYFKRVCSLLWLVLPMLIMPLEVAAQEIIPNEEVTESLAFVAPVEETDAIEAEVEALQEIVTTEEIAEQAVRSYTYTVYRDGVKIASGLTEPTFLDEDVPAGEHTYCVEVQYQEGVSDKVCVDVEVKDFKPVTNLTGTASNDEVSLDWDGVEEKAEEPASDKAVSYNVYKNGTLIGNTAETHYVETGVANGTYIYEVEVKYPDGVSPKVAVTVTVTNSSLSNVDGQAPYTLRVEGKKIIAEAHGMITLYDINGRTVAVAPNRLEYMAQTGFYAVRFDVGNKHHVSKIQVR
>NZ_CP024593.1|WP_099810610.1|1146558_1148496_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein
MISVNNLTVDFGTRLLFDQVSFVINRRDRIALVGKNGAGKSTLLKLIAGMEEPTSGHIARPKGIRIGYLPQVMRLQDGHTVYEEVEQAFNDIRQIEEEIRRLSDEMAGRIDYESDDYIRLIEHYTNMSETLSLMQQGNYHAAIEQTLIGLGFGREDFHRPTADFSGGWRMRIELAKLLLQRPEVLLLDEPTNHLDIESIGWLEQFIATNAGAVILVSHDRAFIDNTTTRTIEIELGHIYDYKTNYSHYVELREERLRQQMRAYENQQKMIRDTEDFIERFRYKATKSVQVQSRIKQLEKVERVEIDERDRSAFHFRFIPAQPSGSYPLIVDDLAKAYGDHRVFSGATYTIERGEKVAFVGKNGAGKSTMVKCIMGELTDYTGKLELGHNVELGYFAQNEAQELRGDLTVFDTIDREAVGDIRLRLNDLLGAFLFGGEASEKKVSVLSGGERARLAIIRLLLQPANFLILDEPTNHLDMRSKDVLKEAIKNFDGTVIVVSHDREFLDGLVSKVYEFADGQVNEHLGGIYDYLRTRRMQTLTELERTTTIETKNTREAIPETEAKADYRRQKEVAKQLRTLERTVATCEERIGKLESELQAIEMLLQDPKHATDANLFERYAGMKQELEKAMEDWEQASEALSEAQG
>NZ_CP024593.1|WP_005874285.1|1148492_1150580_-|tetratricopeptide-repeat-protein
MTFKRSLFFLLLLLSVATARAQIDVDRVITIGRNALYFNDYVVSIGYFNQVVGLRPWMAEPYFYRGIAKISLEDYTGAEADASACLQRNALIPKAYLLRGVARQNLGKIDSAIQDYRRGLELMPNDEGMLVNLTGVLTDSKRYAEAREGVAELLKFYPKSKQAHIALSAIELGEQDTVAAIRELNEVLRMDSLFAPAYSQMAMLHLKSKRNAEAMAALDKAIELEPSELSNYINRGVIRYQSNDLRGAMDDYSHVVRQKPNDKLARFNRALLRSYLGDVNNAIEDFDVVIRLEPENYHALYNRAILLTQINENRKAITDFDKVLGHYPDFVVGYYARSQAKKALGDTRGAERDYWRAFDIEKAAQSKTKKTKKSSSSTSTKETREDSDETIEKFNLLVVSEKSSEKRTRYSSRIRGRIQDNDVEVQPSPLFVLSYYEQSSSEEVPRVYYSEAIARFNDKKVLPKRLKPINREVALSQEQVAYHEQDITEISERTAGNADLCFRRALDYMLIQNLEQAIVDFDQAVELNKQFALAYFGRAIARAKLVEARQGASFIHQEAETVNAMTKALITTPRTNAMGVPAAAESPERKPAISDVDGELVMRDLNRTIELDPNFAYAYYNRAVLLARRGDTDAALSDYDRAIKAYPEFADAYFNRGLLLLSRGKAKEGIADLSRAGEYGLYKAYNIIKRMSTKS
>NZ_CP024593.1|WP_004585605.1|1150615_1151293_-|peptide-deformylase
MSETAYSPCFETGTAFSTQKTREKTITRTQILFDRTMLLPIYLYGHPVLRKVAEDITPDYPKLKELIANMTESMYHSDGIGLAAPQIGLPIRVLVIDADPLKEDYPECAGFKRVMINAHIEERGEDLCTEYEGCLSLPAIHEKVERPTSIRIRYVDEDFQPHEEVLQGFAARVVQHEYDHIDGKLFIDHISPIRKQLIKGKLQNIIKGKVRTSYRVVTAPTGKKR
>NZ_CP024593.1|WP_004585606.1|1151289_1151742_-|Holliday-junction-resolvase-RuvX
MELALVSYFCTDMGRILAIDYGRKRTGLAVTDPLKIIPGGLTTVPTHTLLDFLRDYVSREPVERFVLGLPRRMNYEESESMTYIRPFAVKLAQAFPSIPITYVDERFTSRMAQRTILEAGIGKMKRRDKALVDEVSAVIILQSYLDNPDR
>NZ_CP024593.1|WP_157763375.1|1151859_1152003_+|DUF1661-domain-containing-protein
MAREFFHSRTKTKKFSRHLFQYHKPRFLRAIFPFLRPLHNKQSLLFI
>NZ_CP024593.1|WP_099896732.1|1152204_1157928_+|alpha-2-macroglobulin
MMNIRVIFSLFLALTIGLTAMNAQNPYATLEKELEQYRQERRPRKVAETLKKIRVMAESRRDVPMLLHSMFLYDDPENDINDYPEEPLMNDLDKLMQASWLRPVDRAMILFMRLRMYVRYGQFGSAYMMGAVHGDPKDNRLSLWSEKQFEDAFLRDFDAFLSYRKALLQARTEDFRPLFESQPKKCAAPPRSLYQSCISVLALAVGSSSEADGKISHAFEEELRRAASYLSDRRERLEMETDRLDYEKRRRKLDDAASYRRMDELIAAYSDLPDVIGMVDRRVNAYCDEEEYVSALDLCNSYLSKYPEAPRINLLKSSRASRILASFVKCDYPLRLHTRLPKSMRIASRNVGSVLISLYWLDMNGSQAADIRQEDLHLYAKGTPFWTESIRTQGRADMKMDSIRCTLPDLPKGVYLVKASAEQCVLEKTKPVPQYSLLHVSDLFFLAQQAMPGVQVLDALTGKPVEGASVDASMRYSIDRSVHTLSPTDRYGRINLRKSYNRFFPYTDGDRSYPVVSAYTYKQDQVDLSKKNERKYIVSTDRAIYRPGQKVHFFGQCDRIGYAVEDARAIGGSEVEVVLEDANSKEIGRLLCQADEMGRFSGSFDLPTGILNGLFGLRVGGDTYPFSEEEYKRPTFEVGLRSPDAAYAMGDTLRIRGEAKTFTGIGMRGATVNYRLSLTPYTRRWWGRPVADRVVQTGEAVVDESGYFVIPVSLSRPEGREDYSYCLYTLSADVTAPGGETQTAVLRIPVGKEPKRVDVEVGKYIRANEGNWLATSLPDLTFTLTNTSGQTVEGSIAYFLCDADNERIGRLYTAASGVVTPAPAEWGKLPSGQYRLRFGESGGEDSDFVTKDVYLFRPKDRQLSNPSQGLWTYVAEEKYDSHRPARILVGATPKDADAQELYLFYDLTQAGRFIERKMIACRPGEIVEIVPMLPAAPLPESMNVSLYYVYGGRLYSRSIDLERRLPTREIKMSWSTFRDKLRPGEKETWKLRLADAEGKPLSHTMMAAWMYDAALDKIVHSSVFSSRFFSFADSPASLIRLSFPNSGYRVSGSVEDSYVQVGFKHPVFKTPQLCLWSATGYRYVSSDYYYGPMIFVGYGVPEAKSVDAFPMEEKAARADAVNEAEPESKESGIQESSVRTNFAETAFFEPALLTDERGEVSWSFTLPETLTRWHLLLFAHTKDMRLGMKDESVEVRKDFMLTPNLPRFLRMGDKGTASASIRNGSETMQQGFVRMELFDPATDKLLGGERLPFSVEAGGTVTVSFPLDPVSGYDALGVRLLAESHDFSDGEQHSIVQLPATERVVETIPLILYGGQSQTVDLDSLFPHRSGRPAMGTMALQVVSNPLWVAVQALPVMTDVHEEDAVSVASALYANCIAAALVSGRLLHTPALGESLRHYLAQPLDTLALQKSPLSSDELPWRAEMLAEQNNRQRLQALVASDRLTWTEQMLTDKLKRLQKSDGSWAWHPEMSSNDYLTDYVMTMLVRLSALTAAPEHKEFQAVKRMGWNALDDAASRLMDRMKEYEKKTNSKYKILPERALNYLYLLTIDSRNPSSRGHAARMYFLDILGRSLPHISILDMPRAAIVLHGVGRKALADDFLRSIREHIIRTPDQGAHFALSSGGYYWCDRRYGMQTEAIEAFARIGTSQDSSHIEGLQMWLLNQKRTQLWPSLPASSDAIYALLLGAGKDRMVEATVSVRAPVPALSGTFAGAGESRIVTVGDLPQGNLSAELTRSGKGFAWASFLAEYDAPAADLVATGNGLSVEKHLFSEQVIDGKLTLVPLREGDRLEVGKRLVTQLTITLDRDMDFIVLTDKRAAAVEPIGQLSGYDYAAGTFYYREIKDSSTRFYFDRLVRGSYKLQYSTVVVRSGAYASGIATVSSAYAPEFTGHTDGGRQLQTVPVANTQ
>NZ_CP024593.1|WP_099810615.1|1157941_1158886_+|2-dehydropantoate-2-reductase
MNQQPIKIAVFGLGGVGGYYGAMLALRAAATDGLLEVSWIARGAHLEAIRAAGGLRVVTPSRDFLARPTCVTDNPAEVGTVDYILFCTKDYDMERGVAEIRPMIGQNTKILPLLNGADIAERMRTYLPDTVVWKGCVYISACKSAPGLITLEADRELFYFGSGLPEQTDDEVRLAELLTAAGIRAYNPTDIDWYIMKKFMMISVTATATAYFDKPIGSILTEHEPELLSLLEEVAELFRAKYGQVPDDVVQQLLDKQRKMPPESTSSMHSDFLQGGSTEVETLTGYVVREAEALRVDLPMYKRMYRELVSRTAN
>NZ_CP024593.1|WP_004585610.1|1159021_1160638_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein
MITVNDLSVQFGKRILFQDVNLTFTPGNCYGIIGANGAGKSTMLRVISKQLDPTRGTVTLGPGERLSVLSQDHFAFDENTVMDTVLMGHSVLWAIMEEKNALYAKPDFSDEDGTRVAELEDKFAEMEGWNAESDAAMLLSGLGIKEDLHYMLMKDLSGKQKVRVLLARALYGKPDNLLLDEPTNDLDLETVSWLENYLSNFENTVLVVSHDRHFLDSVCTHTVDIDFGKVQQFSGNYSFWYESSQLALRQQQQQNKKAEEKRKELEEFIRRFSANVAKSKQTTSRKKMLEKLNIEEITPSSRRYPGILFTPGREPGNKILEVKGLTKSIEGQLLFRDLNFNVEKDDKIVFISRDPRAMTALFSIINGEMTPDEGTYEWGQTITTAYLPLDNSGYFNTDLNLVEWLSQFAKDTNEVFLKGFLGRMLFSGEEILKKASVLSGGEKMRCMISKMMMLDANTLVLDTPTNHLDLESIQAFNNTLKTYRGNVLFASHDHEFIQTVANRIIELTPNGIIDKIMDYDDYITDPIVAEMRQKLYGQ

Crispr_ID: NZ_CP024593_8

• CRISPR_ID: NZ_CP024593_8
• CRISPR_location: 1210330-1210425
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP024593_8

Consensus_repeat	Method
GTAATGGTCGTAGAGTCTAGGAGCTTGACG	CRISPRCasFinder

spacers of NZ_CP024593_8

>8.1|1210360|36|NZ_CP024593|CRISPRCasFinder
AAGGGTGGCGACCAATTTTTCCATCATGCAAACGTT

CRISPR arrays and Neighbor proteins around NZ_CP024593_8

CRISPR arrays

The CRISPR arrays of NZ_CP024593_8

>merge|NZ_CP024593|8|1210330-1210425|CRISPRCasFinder
GTAATGGTCGTAGAGTCTAGGAGCTTGACGAAGGGTGGCGACCAATTTTTCCATCATGCAAACGTTGTAATGGTCGTAGAGTCTAGGAGCTTGACG

>NZ_CP024593|8|9|1210330-1210425|CRISPRCasFinder
GTAATGGTCGTAGAGTCTAGGAGCTTGACG	AAGGGTGGCGACCAATTTTTCCATCATGCAAACGTT
GTAATGGTCGTAGAGTCTAGGAGCTTGACG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024593.1|WP_004583425.1|1216551_1217727_+|type-IX-secretion-system-outer-membrane-channel-protein-PorV	unknown	unknown	unknown
NZ_CP024593.1|WP_099810643.1|1211602_1212259_+|redox-sensing-transcriptional-repressor-Rex	unknown	unknown	gnl|CDD|235486
NZ_CP024593.1|WP_099810637.1|1200751_1202101_+|sigma-54-dependent-Fis-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225114
NZ_CP024593.1|WP_099810631.1|1192333_1194913_+|ATP-dependent-Clp-protease-ATP-binding-subunit	unknown	unknown	gnl|CDD|223616
NZ_CP024593.1|WP_099810649.1|1220308_1220620_+|DUF1661-domain-containing-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_099811825.1|1203518_1205699_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_021665681.1|1206473_1207475_-|tRNA-dihydrouridine-synthase-DusB	unknown	unknown	gnl|CDD|239200
NZ_CP024593.1|WP_005874467.1|1218323_1218866_-|RNA-methyltransferase	unknown	unknown	gnl|CDD|349970
NZ_CP024593.1|WP_099810647.1|1212999_1216476_+|type-IX-secretion-system-sortase-PorU	unknown	unknown	gnl|CDD|199210
NZ_CP024593.1|WP_099810639.1|1205783_1206488_+|winged-helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224759
NZ_CP024593.1|WP_099810645.1|1212327_1212987_+|fumarylacetoacetate-hydrolase-family-protein	unknown	unknown	gnl|CDD|223257
NZ_CP024593.1|WP_099896733.1|1195051_1198063_+|serine-hydrolase	unknown	unknown	gnl|CDD|224389
NZ_CP024593.1|WP_021677465.1|1217733_1218222_+|2-C-methyl-D-erythritol-2,4-cyclodiphosphate-synthase	unknown	unknown	gnl|CDD|376811
NZ_CP024593.1|WP_099810641.1|1207471_1209148_-|sulfate-permease	unknown	unknown	gnl|CDD|183265
NZ_CP024593.1|WP_004583416.1|1202111_1203449_+|GHKL-domain-containing-protein	unknown	unknown	gnl|CDD|227333
NZ_CP024593.1|WP_099810651.1|1221668_1224254_-|glycoside-hydrolase-family-2-protein	unknown	unknown	gnl|CDD|225789
NZ_CP024593.1|WP_099810635.1|1199148_1199919_+|2-phosphosulfolactate-phosphatase	unknown	unknown	gnl|CDD|377205
NZ_CP024593.1|WP_004583413.1|1198110_1199139_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl|CDD|273466
NZ_CP024593.1|WP_004583429.1|1219717_1220194_+|cytidine-deaminase	unknown	unknown	gnl|CDD|273572
NZ_CP024593.1|WP_099777647.1|1220823_1221621_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP024593.1|WP_099810643.1|1211602_1212259_+|redox-sensing-transcriptional-repressor-Rex	gnl|CDD|235486	PRK05472, PRK05472, redox-sensing transcriptional repressor Rex; Provisional.	1.37359e-92
NZ_CP024593.1|WP_099810637.1|1200751_1202101_+|sigma-54-dependent-Fis-family-transcriptional-regulator	gnl|CDD|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	1.53794e-167
NZ_CP024593.1|WP_099810631.1|1192333_1194913_+|ATP-dependent-Clp-protease-ATP-binding-subunit	gnl|CDD|223616	COG0542, clpA, ATP-binding subunits of Clp protease and DnaK/DnaJ chaperones [Posttranslational modification, protein turnover, chaperones].	0
NZ_CP024593.1|WP_021665681.1|1206473_1207475_-|tRNA-dihydrouridine-synthase-DusB	gnl|CDD|239200	cd02801, DUS_like_FMN, Dihydrouridine synthase-like (DUS-like) FMN-binding domain. Members of this family catalyze the reduction of the 5,6-double bond of a uridine residue on tRNA. Dihydrouridine modification of tRNA is widely observed in prokaryotes and eukaryotes, and also in some archaea. Most dihydrouridines are found in the D loop of t-RNAs. The role of dihydrouridine in tRNA is currently unknown, but may increase conformational flexibility of the tRNA. It is likely that different family members have different substrate specificities, which may overlap. 1VHN, a putative flavin oxidoreductase, has high sequence similarity to DUS. The enzymatic mechanism of 1VHN is not known at the present.	1.59888e-109
NZ_CP024593.1|WP_005874467.1|1218323_1218866_-|RNA-methyltransferase	gnl|CDD|349970	cd18097, 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.	6.00061e-72
NZ_CP024593.1|WP_099810647.1|1212999_1216476_+|type-IX-secretion-system-sortase-PorU	gnl|CDD|199210	cd02258, Peptidase_C25_N, Peptidase C25 family N-terminal domain, found in Arg-gingipain (Rgp), Lys-gingipain (Kgp) and related proteins. Peptidase family C25 is a unique class of cysteine proteases, exemplified by gingipain, which is produced by Porphyromonas gingivalis. P. gingivalis is one of the primary gram-negative pathogens that causes periodontitis, a disease that is also associated with other diseases such as diabetes and cardiovascular disease. Gingipains are a group of extracellular Arg- and Lys-specific proteinases called Arg-gingipain (Rgp) and Lys-gingipain (Kgp); RgpA and RgpB are homologous Arg-specific gingipains encoded by two closely related genes, rgpA and rgpB, while Lys-specific gingipain is encoded by the single kgp gene. Mutant studies have shown that, among the large quantities of proteolytic enzymes produced by P. gingivalis, these three proteases are major virulence factors of this bacterium. All three genes encode an N-terminal pre-pro fragment, followed by the protease domain; however, rgpA and kgp also encode additional C-terminal HA (hemaglutinin/adhesion) subunits which consist of several sequence-related adhesion domains. Although unique, their cysteine protease active site residues (His and Cys) forming the catalytic dyad are well-conserved, cleaving the C-terminal peptide bond with Arg or Lys residues. Gingipains are evolutionarily related to other highly specific proteases including caspases, clostripain, legumains, and separase. Gingipains function by dysregulating host defense and inflammatory responses, and degrading host proteins, e.g. tissue, cells, matrix, plasma and immunological proteins. They are proposed to enhance gingival crevicular fluid (GCF) production through activation of the kallikrein/kinin pathways, thus increasing vascular permeability and causing gingival inflammation, a distinctive feature of periodontitis. RgpA and RgpB are also able to cleave and activate coagulation factors IX and X in order to activate prothrombin to produce thrombin, which in turn increases production of GCF. The gingipains also play a pivotal role in the survival of P. gingivalis in the host by attacking the host defense system through cleavage of several immunological molecules, while at the same time evading the host-immune response by dysregulating the cytokine network.	5.7756e-131
NZ_CP024593.1|WP_099810639.1|1205783_1206488_+|winged-helix-turn-helix-transcriptional-regulator	gnl|CDD|224759	COG1846, MarR, Transcriptional regulators [Transcription].	9.40563e-12
NZ_CP024593.1|WP_099810645.1|1212327_1212987_+|fumarylacetoacetate-hydrolase-family-protein	gnl|CDD|223257	COG0179, MhpD, 2-keto-4-pentenoate hydratase/2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) [Secondary metabolites biosynthesis, transport, and catabolism].	5.40066e-60
NZ_CP024593.1|WP_099896733.1|1195051_1198063_+|serine-hydrolase	gnl|CDD|224389	COG1472, BglX, Beta-glucosidase-related glycosidases [Carbohydrate transport and metabolism].	5.33536e-77
NZ_CP024593.1|WP_021677465.1|1217733_1218222_+|2-C-methyl-D-erythritol-2,4-cyclodiphosphate-synthase	gnl|CDD|376811	pfam02542, YgbB, YgbB family. The ygbB protein is a putative enzyme of deoxy-xylulose pathway (terpenoid biosynthesis).	1.5438e-102
NZ_CP024593.1|WP_099810641.1|1207471_1209148_-|sulfate-permease	gnl|CDD|183265	PRK11660, PRK11660, putative transporter; Provisional.	8.26492e-162
NZ_CP024593.1|WP_004583416.1|1202111_1203449_+|GHKL-domain-containing-protein	gnl|CDD|227333	COG5000, NtrY, Signal transduction histidine kinase involved in nitrogen fixation and metabolism regulation [Signal transduction mechanisms].	1.06725e-32
NZ_CP024593.1|WP_099810651.1|1221668_1224254_-|glycoside-hydrolase-family-2-protein	gnl|CDD|225789	COG3250, LacZ, Beta-galactosidase/beta-glucuronidase [Carbohydrate transport and metabolism].	9.31982e-97
NZ_CP024593.1|WP_099810635.1|1199148_1199919_+|2-phosphosulfolactate-phosphatase	gnl|CDD|377205	pfam04029, 2-ph_phosp, 2-phosphosulpholactate phosphatase. Thought to catalyze 2-phosphosulpholactate = sulpholactate + phosphate. Probable magnesium cofactor. Involved in the second step of coenzyme M biosynthesis. Inhibited by vanadate in Methanococcus jannaschii. Also known as the ComB family.	2.58215e-81
NZ_CP024593.1|WP_004583413.1|1198110_1199139_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl|CDD|273466	TIGR01140, L_thr_O3P_dcar, L-threonine-O-3-phosphate decarboxylase. This family contains pyridoxal phosphate-binding class II aminotransferases (see pfamAM:pfam00222) closely related to, yet distinct from, histidinol-phosphate aminotransferase (HisC). It is found in cobalamin biosynthesis operons in Salmonella typhimurium and Bacillus halodurans (each of which also has HisC) and has been shown to have L-threonine-O-3-phosphate decarboxylase activity in Salmonella. Although the gene symbol cobD was assigned in Salmonella, cobD in other contexts refers to a different cobalamin biosynthesis enzyme, modeled by pfam03186 and called cbiB in Salmonella. [Biosynthesis of cofactors, prosthetic groups, and carriers, Heme, porphyrin, and cobalamin].	2.20574e-68
NZ_CP024593.1|WP_004583429.1|1219717_1220194_+|cytidine-deaminase	gnl|CDD|273572	TIGR01354, Cytidine_deaminase, cytidine deaminase, homotetrameric. This small, homotetrameric zinc metalloprotein is found in humans and most bacteria. A related, homodimeric form with a much larger subunit is found in E. coli and in Arabidopsis. Both types may act on deoxycytidine as well as cytidine. [Purines, pyrimidines, nucleosides, and nucleotides, Salvage of nucleosides and nucleotides].	8.66148e-54

Protein sequences

>NZ_CP024593.1|WP_099810641.1|1207471_1209148_-|sulfate-permease
MIGSYFRPKLLDVFHGYNRERFMADLMAGVIVGIVALPLAIAFGIASGVSPETGLITAIIGGFIVSLLGGSSVQIGGPTGAFIVIVYGIIHKYGIEGLTIATIIAGILLLVMGVLRLGTLIKFIPYPIVVGFTAGIALTIFSTQMNDLFGLGITDMPGDFLGKWGAYFTNFKSVNLWAFGMGLLSIVIIMLSPRFTKKIPGSLIAIILMTVAAYLLRLQGIGEFETIGDRFTISAQLPKPTGVTLSLETIRQLFPPAFTIALLGAIESLLSASVADGVIGEKHNSNTELIAQGAANIVVPFFGGIPVTGAIARTMTNINNGGRSPIAGIIHAFVLLLILLFLGPLTAYIPMACLAGVLIIVSYNMSGWRSVANIGRGPRSDSLVMLVTFLLTVILDLTVAIEIGLLLAILLFMKRVTENTRITVATGRLDLTQTGEIAHHDEVLDIPKGVEVYEIEGPFFFGIANRFEEIMNTLGDHPDVRIIRMRHVPFMDSTGMHNLENLIKMSRKEGVSIVLSGVRKDVHEELATAGIVELLGEENVCADIQAALRQAQAIAQGT
>NZ_CP024593.1|WP_021665681.1|1206473_1207475_-|tRNA-dihydrouridine-synthase-DusB
MKIGAIDLGVEPLLLAPMEDVTDVAFRIMCKQFGADLVYSEFLSADALIRQVAGTFRKMAIDESERPMAVQIYGRDVASMVEAARLCESAGPDLIDLNFGCPVKRVAGKGAGSGMLRNIPLMIEITREVVKAVKLPVTVKTRLGWDNDSKIIVDLAEQLQDCGIAALTIHGRTRAQMYTGTADWTLIGEVKNNPRMQIPIIGNGDVTTPQEARRAFDVYGVDAVMVGRASIGQPWIFEDMKHFLRTGETLPSRPFSYYMDILRRQTLNNIRKLDERRGILHTRRHIAASPIFKGIPNFKPMRVAMLRATTQEGLFALMDEVEKMIGSADSAAV
>NZ_CP024593.1|WP_099810639.1|1205783_1206488_+|winged-helix-turn-helix-transcriptional-regulator
MKYKKLLFDLIDYLDAFESLHDGGSHEPEIKDFADFLSWRCGKKKKQKEEVVSVTRERAAGAKNIARGVSLLHRYSRFYIKKALTESPLQTEDEYTYLVSLMNGESMTKTELNNLNAMEKTSGAEVMRRLLKANLIEQRPDEEDRRSMRVSITPEGRKVLVNLFPNLRLCTETLVSALSDEQLTAFDHLLWLLCECHNEMFTGKHDAELTDLHAETCGLKQSAGGALSKRLYRR
>NZ_CP024593.1|WP_099811825.1|1203518_1205699_+|hypothetical-protein
MVGQSLPSVSKEIRELSNRTEQQTSLSDRKESEAFALETVRMISDRTPYLFRLAEGRSWEADVRGRSWASRVLPIVHRLKHGGIPWKQYLSSDSLCMEARLYGKYDSVTGAYRRGVVSFRSDIPQRNKVDDLTALALLGENVYAEEFDFGNRQIFPNPIRREAEAFYTYRLDSLYEKDGITYRRIAFRGLSGLNHGTVTIDATHGQLAILEMRVMMKGVITESYRVELGEVEPDFFLPIGLSVVIDRNRLWASLHNGYSASISYTGEQLDKTVLPVYMPTDSSRYRLPDELPVAPVWAVRSSFGREDSSTYWKNVVVGRDHTLHQHVPWHRALAWGHKYRIGERWRLGNEGLVWALFYYNYADHLWLGQSLTAIYDMAPGIRWEIKPGLYYVTKRRKAVWTLDSKLYYSPSQRGLLQLSAGHRSFDLYSTRERIDQLTDLMMELLNGQGPTTRYDDKFVRLTNSIDLLPKLNVETSVMLAERNPLPHGETWSLFGGSITDILNISNADPDLPRIVPHHRLLEVRAKMTFNPRPYYRYTADGFLIREGEGIRAPLLSLSYRGAFGMGRKSDARFHHLDLSIQQRLVFSPAASLFYQLNVGGYFDRSVIYPSEYFFLKGGNAFWRFGDSMEAAFQTLPPYTATADKHLILQTSYRASRLLVNFLPLVFLKTNDEALHFKARWDMVSRKPYLEMGYSESIGTLMQVGVFYGGYNFFYERGVAIRFTFNM
>NZ_CP024593.1|WP_004583416.1|1202111_1203449_+|GHKL-domain-containing-protein
MGRRKTGSFGLHLLFTIVMAVVGTWSAAAGHYAITVFAAGLVIFSALRLRLLYRRHLQDFSLLLNAIENGDYSVRFSEMGGNVSHRTFNRTLNRIKEILSRSRDEAIAGEQFLVHVLEQIPVGIMMVAPEGYVYSTNTVLLRLLGLPVITHLDQLRRVSPDMPRLFRSAATDSGIHIKLTTEREEQEVSLRFSSFRIRGKIYHIYTLSNIGKELDARETESWIRLIRVMTHEIMNSIAPITSICDTLLDNLQSSADEEMLSTGLDTIRSTGVGLLSFVQDYRKFTAVPPPEKEDIALHAFLSGILRLQEELLSSNDIKVDIEEIPVELTVPADRRQLTSVLINLVKNAAEAEYPADTEKRLLRIRVEERLDSLDEHRLLLHVENNGTPIPQEVFDNMFVPFYTTKTGGSGIGLSLSRYIIRLHGGNLLARRTADGFTSFVIELPL
>NZ_CP024593.1|WP_099810637.1|1200751_1202101_+|sigma-54-dependent-Fis-family-transcriptional-regulator
MKKSGNIIVVDDNKHVLTALKLLLTGSFETVTLLPSPKTLLSTIVEVHPDVLLLDMNFSTGINTGNEGLYWLDQVRSRFPDLPVVLFTAYADIRLAVEALKRGASDFVVKPWNNAELLESLRMAMNKAASTQVTATPKEDDSVFLGKSKAMREVLELADRIGDTAAHVLITGENGTGKGVLAEYIHARSPRSRQPMLTVDMGALSETLFESELFGHVKGAFTDAKSDRAGKFETASGGTIFMDEIGNLSLALQAKLLAVLQQKVVTRVGSNTPIPVDVRIISATNSDLPLSVAEGRFREDLLYRLNTIHIEMPPLRRRREDIAPMAVFFLHRYARQYGKEVPELTPEAEALLSDYPWPGNVRELQHCIEKAVILSRSSSLSAADLSLPKSVDAHPTATGVASTPQTLDEMEKTAIEQALARNGSNLSNVARELGISRQTLYNKMKRYGL
>NZ_CP024593.1|WP_099810635.1|1199148_1199919_+|2-phosphosulfolactate-phosphatase
MLQISLCPSPVLYPYYKTEQEEYTVVIVDIFRAGTTITTALMNGAVGIIPIATVEEAEIYAGNGFLVGGERGTKRLPFAHFGNAPEEYTRQAVEGKQLVLSTTNGTRAADIAAGALHVIIGAFINLEAVARYCIAKQKPVMVLASGWQNRMSTEDCLFAGALAATIVRLGEEVICEDGATVFQELWGNYNTHEKLTAYLNGRDHYERLRANKLERSVPYCTSLNLTEIVPELTFKISAASTDCPANRLFLPVTPPF
>NZ_CP024593.1|WP_004583413.1|1198110_1199139_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MIFGHGDEGITPLSSEIVNFSTTVWTDGDKDHLEKHLVENLNCIRHYPEPDAGTLRQMLAKRNSVDNNAILVTNGPTAAFYQIAQAFRGSRSLIAIPSFAEYEDACRMYEHEVCFYPSNEDIGEADFSNMDFCWLCNPNNPDGRLLQRTEILRLLNDHPDTTFVLDQSYVSFTTEEVIRPADIKGRKNLVMVYSFSHAYGIPGLRIGYIVANKDFMKRVAAFSTPWAVNALAIEAAKFILIHPAQFTLPIRKWQRNTVDFITALNRLDGVEVHPSGTTFFLLRLKKGTAAELKKYMLEEYNMLIRDASNFRGLDESYVRITTQRPAQNQLFIKALETFLEKY
>NZ_CP024593.1|WP_099896733.1|1195051_1198063_+|serine-hydrolase
MKRFLFSAITILSLSVLYTATAPARTNMGAMHAQQSKDYPFLLFGGVESKDVKRWVDDRMKAMSTEEKVGQLLMPIVYPSLQEEKVKQAEQLVRTCHIGGILFQKGTLSEQYTMTRRLQEAAGTPLLIALDGEWGLHMRLKDAPRFPRNMGLGHQKDNQLLYNYGREVARQCRLMGIHINFAPVLDVNNNPKNPVIGTRSFGDNPRRVAERGIAYAQGLEDGGVMAVAKHFPGHGNTTEDSHKTLPTVFASREELENTELFPFKEFFRAGLSGVMTAHLNVPALEAKKNTPSSLSHAICTDLLRQEMGFKGLIFTDGLAMQGVQTAGSQPISVRAILAGNDILLGPVDPVKTFSEVLAAVEDRTISKELLDEKCRKILAFKYALIICKGISKEVPAEEVVRQVNSREAERMSEDLWRASITILKNKKQFLPLSEENRIACVNLDGAASNTFTQELGLTSKDCYSYAKGSNSTRTQELLSKLKGYDAVIVTVRHTQPDWAGTFLHRLTEQNHTAIVFFTSPYVADRIPVAMDKARAIVVAYENVKEAARMAAYKIRDRVVVSSGGGIPVVQEEEDTDPTANMMPPTELSSGLIPMPAVDRIAKEALRQGAFPGCRILAVHRDKVVYDKSFGTLDGSARGGKVSSSTIYDLASVTKVVATTPAVMLLVQDGKLKLSDRLGTLLPRFARTDLKDITVQQLLLHEAGLRPSINFYESLIDSSSLDGKLLSPRRSSGWVRVDTNMWGNPFFGFRSDLVSGQFRPDYPFRFSSNLYLSKEVKEIVLNTIASTPRNGVGRYKYSDLGFILLQQIVEKVSGKSLNVFVEERIFRPIGAGSLGYLPLDKYSVSRIAPAQNDKFLRKSIVRGTVDDEAAACLGGISGNAGVFGTAEDVARVLDMFIHEGTYKGHRIIDQKIFRLFITTHGKGNRRCLGFDKGRASMAESASGSTYGHTGFTGTCVWVDPENELIFVFLSNRTYPNRLNKTLMTASIRPRLHQAIYEALGIAEQ
>NZ_CP024593.1|WP_099810631.1|1192333_1194913_+|ATP-dependent-Clp-protease-ATP-binding-subunit
MAYDFTQTFRNSLEYSYQEATRLGVVAVTQDMLVLGIIRDGDNGAIDIMRHYGINLYELKRLIELEAIAESLPASPEESPIFTPSAREAIDDATDICADLEDEAVSPVHLLLSILNSTQESLVQKIFMKQGIKYDTILSDYFGQRNPSEGKSPSEMEILDGYQDNDFDDEEDESSPPSGNGGAGGGSGDAPEQNTGGGDTTTTTRSGGDTPALDTFGTDITAMAAAGKLDPVVGREQEIERVIQILSRRKKNNPVLIGEPGVGKSAIVEGLAERIVNRKVSRILFDKRIISLDLAQMVAGTKYRGQFEERLKAVLDELKKNPQIILFIDEIHTIVGAGSAAGSMDTANMLKPALARGQVQCIGATTLDEYRKNIEKDGALERRFQKVPIAPSTAEETLTILQNIKEKYEDYHGVRYTDEAIKAAVELTDRYVSDRFFPDKAIDAMDEAGASVHITNVVAPKEIEILEAELASVRENKLLAVKAQNYELAASFRDQERRTQQQIVEEKKKWEEQMSKHRETVDENVVAHVVALMTGVPAERLSTGEGERLRTMADDLKTKVVGQDTAIEKMVRAIQRNRLGLRNEKKPIGSFLFLGPTGVGKTYLAKKLAEYLFEDENAMIRVDMSEYMEKFSVSRLVGAPPGYVGYEEGGQLTERVRRKPYSVVLLDEIEKAHADVFNLLLQVMDEGQLTDSLGRRVNFKNTVIIITSNVGTRQLKDFGQGIGFRSEKDEEANKEHSRSVIQKALNKTFSPEFLNRLDDIILFDQLGKTEIRRMVDIELKAVLARIHRAGYDLVLTDEAKDVIATKGYDLQYGARPLKRTLQNEVEDRLTDLILSGQIEKGQTLTLSARDGEIIVQEQA
>NZ_CP024593.1|WP_099810643.1|1211602_1212259_+|redox-sensing-transcriptional-repressor-Rex
MKTIANESSLLDTKVPEPTLRRLPWYLSYVQLLHADGCESVSSTRIARAVGVDASLVAKDLSYVSVDGRTRVGYRVADMVAVLNDFLGFTHHHRAFLFGVGSLGAALLQDSGLRHFGLEIAAGFDVNPDIVDTNINGIPVYHKSRVAELCARERVDIGILTVPIRAAQSMADEMIAAGIKAIWNFTPRRISVPEGVVVQNTSMYAQLAVMFNRMKSLP
>NZ_CP024593.1|WP_099810645.1|1212327_1212987_+|fumarylacetoacetate-hydrolase-family-protein
MKIIAVGMNYGAHVSEMRRADILPVAPCPDGERAGFCVEEPVLFLKADSLLREGHPFFYPDFSQEIHYETELVVRIDRIGKCIAERFAHRYYSEVTVGIDFTARDLQRRAKAKGLPWATAKAFDNSAAVGRWVKKDSLRHGVQELGLRLDIDGRTVQQGNTRDMLFSVDRLIAYASRFFTLRMGDLIFTGTPAGVGPIAIGQHLEAYLEEQKLLDISIK
>NZ_CP024593.1|WP_099810647.1|1212999_1216476_+|type-IX-secretion-system-sortase-PorU
MKRILPIVAFFSLFLALALPAKAQRAMGKTADRSLMASGHWVKIRVDASGVYRLTDEQLRANGFSDPSKVGVFGYGGGVLPEDLSRITTDDLPPVPVLRQGNALYFYAVGPVTWFYNPAKTTMEHTVNTYSTHGYYFLSDAAGAPLQMSQYTGGGASAEALIDYYDELMLHEQELYSPKESGRDLYGESFSAVNTRTVKFPLRGNTRSSGELGTVFSYIAKARSAGGGREMSLSANGILIFSDPFSMTSNEVSNSYLAGKKRRLYHSTPMNSLVNELRLDANYSMTGDAVNLDFIEVATQNDLRYDGAPMHIRRFSNLPVLGGESCRFVISEVPESLVVLHANSSLTASLVPVKTVGDKTIEFVAPLKDQDRRTINTFYAVDLSQASAPEILGAVPNQNLHGEEIPDLIIVSTQALLPEADRLATYRREKNGLKVLVVLQEQVFNEFSGGTPDATAYRLFAKMFYDRWKANAPVGETFPMQMLLFGDGAHDNRKVSVAWQKPYLQQTEFLLTFQAVNSTNVNSYVTDDYFGLLDDQPASVNIGWRNYNMAVGRFPVRTPAEARIAVDKTIRYEEDRESGAWRIRACFAADNGDKHATETSRLIDTVKRYAPAIMPVRAFQDVYPHVIENGLHSIPGAKKKMLETLQSGIILLNYAGHGGPAGWSDEHLLTLNDIHNFNYKHMPIWITATCDFANYDSQTTSAGEEVFLHEKSGTPIMFSTTRVVYNTQNEKINGFMLRRMFEKAKDGRYRTMGEIIRSAKQGMLSTVFPDSINQLSFFLMGDPSVRMNLPTHKVQLTAINGQDPEGQYGTIMLKSLERVALKGKVTDEKGTFDETFSGKVFLTVFDGRKKMTALEEEGNDLSLVYYDYPNVMYAGIAEVKDGLFETSFIVPKDVNYSEHEGRINLYAYNESIKAEAMGVDFSIRVQPGIPDEVTEDNTPPEIISCFLNDSTFRSGDEVNPTPLFMAEVFDLNGINITGSGVGHDITLCIDGRADLTYNLNAYFTSSATDAGVGTILFMIPALAEGDHTARLTVWDIFNNAVHHDFSFRVVDGIAPDVADVILFPNPVRESATFRIFHNRPGSDLNVAVEIYDFTGRLVNSLPVKTYSSSYGEPIEIKWDLTSKYGVKIGNGFYLYRCVVNSPGGQTASMAKKMIVVGQ
>NZ_CP024593.1|WP_004583425.1|1216551_1217727_+|type-IX-secretion-system-outer-membrane-channel-protein-PorV
MIIKKMLKNKLAPLAILFLFAPKAMKAQEQLNVVHTSVPSLNISPDARAAGMGDIGVATTPDAYSQYWNPSKYAFMDTKAGISFSYTPWLSKLVNDIALMQMTGFYKLGTDENQAISASLRYFTLGKLETFDELGESMGEAHPNEFAVDLGYSRQLSENFSMAVALRYIRSDQSTHNTGENQAGNAFAADIAGYLQKYVLLGNAESLWSLGFNVKNIGTKISYDGGVTSFFIPTSLNLGTGLLYPIDDYNSINFNLELSKLLVPTPPIMDQNDQAGYEAALKKYQETSSISGIFSSFGDAPGGLKEEFREITWGLGAEYSYDDKFFVRAGYSYLHPTKGNLQYFTAGAGFKMNIFRIDASYLLSTIQSNPLDQTLRFTLAFDMDGLRNLFH
>NZ_CP024593.1|WP_021677465.1|1217733_1218222_+|2-C-methyl-D-erythritol-2,4-cyclodiphosphate-synthase
MKKPFRIGFGFDVHRLSEGYPLWMGGVRLEHSKGLEGHSDADVLIHAICDALLGAAALRDIGYHFPPSDPQYKGIDSKILLARVMELVRSQGYELGNIDATIAAEQPKLNPHIPDMQRVLAEVMQVEVSDISLKATTTEKLGFTGREEGISAYAVALLIAAV
>NZ_CP024593.1|WP_005874467.1|1218323_1218866_-|RNA-methyltransferase
MRKKKTIEIQRLKTEEYHESPKLPIRIILDDIRSMNNVGSVFRTADAFRLEGLCLCGITARPPHPDIHKTALGAEDSVKWEYFSSVVDAIEELKAKGYSICAIEQAEGSLSLENFSPSKGTRYALIFGNEVKGVRQEAIDLCDLCLEIPQFGTKHSLNVSVTAGIVIWQLVKPLLPLLKK
>NZ_CP024593.1|WP_004583429.1|1219717_1220194_+|cytidine-deaminase
MLRKTLSTPYDIIPRSDFSADVLRLEGAAIEAARSAYAPYSRFSVGAAVLLDNGEILSGSNQENAAYPSGLCAERTVLFYAGARYPEAAVREMVLVAFSASGRVPLITPCGACRQVMLEVCSRHRPFPILMVGEEEAVRVSDVRLLLPFSFDGSDLER
>NZ_CP024593.1|WP_099810649.1|1220308_1220620_+|DUF1661-domain-containing-protein
MSFYLHLKPNDLEAAPSSRSLCSRRITKEYDLQLLVLFLWYVRLDRTGVISRTRKVYTPKFLRLWSLKTWRENFLLLAWEVKNSRATTKKFRCHFWEKHRPQF
>NZ_CP024593.1|WP_099777647.1|1220823_1221621_-|hypothetical-protein
MQIAREETRKSGANILYVINHQRPSIFGSSMHQIGGLMLLSDSVVRNEGEGYPDSPLYDSGQRGKIGSRIKAPVHDLSLHFGPSIITNRTKGLSYSEQQLEKKLSNGLSFVLQYKCHPKGNLYGFGLIASRYEADITKKIEHQGIGFSNRLDYIAPLFSMSTALSERWLLGMSFGLGYLGFRQTLTDISDPKREGYISGSTVGANTALNIGYKLNKHLGIGGEIMMVGGVFHPDNIKTTNISAPKPKEKMGANRFDFTIGLHVYL
>NZ_CP024593.1|WP_099810651.1|1221668_1224254_-|glycoside-hydrolase-family-2-protein
MISKNTFRTFLLWLIPIFMTLQTQAAHTISADTLHLDKGWEFSRHDSTAWLPATVPGVVQYDLIRHGLLPDPNYRLQEEQAQWPEEHDWDYRLLFSLTEQQLRSPRAILMAEGLDTYATVFLNGKKIMESHNMFVGREADITDLLRQSGNELLIRFRSPMKEVRPLRQRDGFDYPADNDHHNEKLSVYTRKAPYQYGWDWGPRLVTTGVWRPVGIRFEGAVAFASKPEVTYTLTKDAQVNCLFPLSWNEQNDRSVRLVVELYSPNGRKVHSEELTAGYGQPSCRTSFTVSSPDRWMPNGIGLPLMYTLVARLQDKDGTTWQTYRTQIGFRTVEFVREEDTHGRSFFFRINGKPLYMKGANYIPGTMMLSARTEEYWQELFRSVSEANMNMLRVWGGGIYEDERFYELADANGILIWQDFAFACTPYPGDEEFLRNVREEADYNIRRLREHPSLALWCCNNEIQEGLKYWGWQKRFDRSTYQKFLTDYDKLFCRLLPERVAALDPTHAYVETSPDTANWGRPATLVWGDSHYWGVWYGREPFGILRERIPRFMSEFGFESFPERKTLESFAWPEDMQLDSPVMKARQKSSVGNEIILEYMRRDYPEPKDFDDFVFKSLIMQGQGMRIGLEAQRAAKPYCMGSLYWQLNDAWPTISWSGIDYYGNWKPLHYQVRRAFEPVIIVPDAERRTISIVSDAPEAKGEDRMALRIEPISFEGKRYPTFWVRNIEVDNEHPTVLPFPIEQWLPQELQRTNLLRLSLVEDVGEAYGEVWASTLYYHHSPKDLLLPVAPPISQELRRTGLRTWELTVRSPYLVKDLFVETDALGARFSDNAFDLLPNEERRLIITLPTDSTEDPVIRLRHL

Crispr_ID: NZ_CP024593_9

• CRISPR_ID: NZ_CP024593_9
• CRISPR_location: 2087882-2087978
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP024593_9

Consensus_repeat	Method
CACCACGATGAGAAGAATAGAATTGTAAGCAA	CRISPRCasFinder

spacers of NZ_CP024593_9

>9.1|2087914|33|NZ_CP024593|CRISPRCasFinder
TCCTCCACGATCTCGGTGTCTGATCTGCTTTTT

CRISPR arrays and Neighbor proteins around NZ_CP024593_9

CRISPR arrays

The CRISPR arrays of NZ_CP024593_9

>merge|NZ_CP024593|9|2087882-2087978|CRISPRCasFinder
CACCACGATGAGAAGAATAGAATTGTAAGCAATCCTCCACGATCTCGGTGTCTGATCTGCTTTTTCACCACGATGAGAAGAATAGAATTGTAAGCAA

>NZ_CP024593|9|10|2087882-2087978|CRISPRCasFinder
CACCACGATGAGAAGAATAGAATTGTAAGCAA	TCCTCCACGATCTCGGTGTCTGATCTGCTTTTT
CACCACGATGAGAAGAATAGAATTGTAAGCAA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024593.1|WP_004585532.1|2081273_2081693_-|large-conductance-mechanosensitive-channel-protein-MscL	unknown	unknown	gnl|CDD|376605
NZ_CP024593.1|WP_005875438.1|2088598_2089933_-|PhoH-family-protein	unknown	unknown	gnl|CDD|224787
NZ_CP024593.1|WP_004585537.1|2087981_2088551_+|crossover-junction-endodeoxyribonuclease-RuvC	unknown	unknown	gnl|CDD|234587
NZ_CP024593.1|WP_012458032.1|2096749_2097322_+|peptidylprolyl-isomerase	unknown	unknown	gnl|CDD|223976
NZ_CP024593.1|WP_023847284.1|2094862_2095024_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_004585526.1|2075980_2077180_+|lipid-A-deacylase	unknown	unknown	unknown
NZ_CP024593.1|WP_004585540.1|2090089_2091757_+|formate--tetrahydrofolate-ligase	unknown	unknown	gnl|CDD|237403
NZ_CP024593.1|WP_005873416.1|2096168_2096699_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_043889970.1|2092677_2093580_-|IS982-like-element-IS195-family-transposase	unknown	unknown	gnl|CDD|372648
NZ_CP024593.1|WP_004585529.1|2079310_2079625_-|NAD(P)-transhydrogenase-subunit-alpha	unknown	unknown	gnl|CDD|378941
NZ_CP024593.1|WP_004585525.1|2075003_2075984_+|SPFH/Band-7/PHB-domain-protein	unknown	unknown	gnl|CDD|223407
NZ_CP024593.1|WP_004585530.1|2079738_2080896_-|Re/Si-specific-NAD(P)(+)-transhydrogenase-subunit-alpha	unknown	unknown	gnl|CDD|240629
NZ_CP024593.1|WP_088493045.1|2097471_2098578_+|chorismate-synthase	unknown	unknown	gnl|CDD|376510
NZ_CP024593.1|WP_005875443.1|2084831_2086142_+|pyridoxal-phosphate-dependent-aminotransferase	unknown	unknown	gnl|CDD|99734
NZ_CP024593.1|WP_099811262.1|2086270_2087380_-|hemagglutinin	unknown	unknown	gnl|CDD|284979
NZ_CP024593.1|WP_088442668.1|2077325_2079314_-|NADP-transhydrogenase-subunit-beta	unknown	unknown	gnl|CDD|376743
NZ_CP024593.1|WP_077070452.1|2082115_2082370_+|DUF1661-domain-containing-protein	unknown	unknown	gnl|CDD|285160
NZ_CP024593.1|WP_099811848.1|2095785_2096196_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP024593.1|WP_004585541.1|2095171_2095738_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|274357
NZ_CP024593.1|WP_043895888.1|2082731_2084789_+|acetate--CoA-ligase-family-protein	unknown	unknown	gnl|CDD|223972

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP024593.1|WP_004585532.1|2081273_2081693_-|large-conductance-mechanosensitive-channel-protein-MscL	gnl|CDD|376605	pfam01741, MscL, Large-conductance mechanosensitive channel, MscL.	1.36432e-65
NZ_CP024593.1|WP_005875438.1|2088598_2089933_-|PhoH-family-protein	gnl|CDD|224787	COG1875, COG1875, NYN ribonuclease and ATPase of PhoH family domains [General function prediction only].	5.95607e-146
NZ_CP024593.1|WP_004585537.1|2087981_2088551_+|crossover-junction-endodeoxyribonuclease-RuvC	gnl|CDD|234587	PRK00039, ruvC, Holliday junction resolvase; Reviewed.	2.9041e-75
NZ_CP024593.1|WP_012458032.1|2096749_2097322_+|peptidylprolyl-isomerase	gnl|CDD|223976	COG1047, SlpA, FKBP-type peptidyl-prolyl cis-trans isomerases 2 [Posttranslational modification, protein turnover, chaperones].	9.29258e-39
NZ_CP024593.1|WP_004585540.1|2090089_2091757_+|formate--tetrahydrofolate-ligase	gnl|CDD|237403	PRK13505, PRK13505, formate--tetrahydrofolate ligase; Provisional.	0
NZ_CP024593.1|WP_043889970.1|2092677_2093580_-|IS982-like-element-IS195-family-transposase	gnl|CDD|372648	pfam13612, DDE_Tnp_1_3, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contains three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction.	8.88486e-100
NZ_CP024593.1|WP_004585529.1|2079310_2079625_-|NAD(P)-transhydrogenase-subunit-alpha	gnl|CDD|378941	pfam12769, PNTB_4TM, 4TM region of pyridine nucleotide transhydrogenase, mitoch. PNTB_4TM is the region upstream of family PNTB, pfam02233, that carries four of this transporters transmembrane regions. PNTB is the beta-subunit of pyridine nucleotide transhydrogenase. This family forms part of the Proton-translocating Transhydrogenase (PTH) Family.	4.858e-30
NZ_CP024593.1|WP_004585525.1|2075003_2075984_+|SPFH/Band-7/PHB-domain-protein	gnl|CDD|223407	COG0330, HflC, Membrane protease subunits, stomatin/prohibitin homologs [Posttranslational modification, protein turnover, chaperones].	5.91634e-63
NZ_CP024593.1|WP_004585530.1|2079738_2080896_-|Re/Si-specific-NAD(P)(+)-transhydrogenase-subunit-alpha	gnl|CDD|240629	cd05304, Rubrum_tdh, Rubrum transdehydrogenase NAD-binding and catalytic domains. Transhydrogenases found in bacterial and inner mitochondrial membranes link NAD(P)(H)-dependent redox reactions to proton translocation. The energy of the proton electrochemical gradient (delta-p), generated by the respiratory electron transport chain, is consumed by transhydrogenase in NAD(P)+ reduction. Transhydrogenase is likely involved in the regulation of the citric acid cycle. Rubrum transhydrogenase has 3 components, dI, dII, and dIII. dII spans the membrane while dI and dIII protrude on the cytoplasmic/matrix side. DI contains 2 domains in Rossmann-like folds, linked by a long alpha helix, and contains a NAD binding site. Two dI polypeptides (represented in this sub-family) spontaneously form a heterotrimer with dIII in the absence of dII. In the heterotrimer, both dI chains may bind NAD, but only one is well-ordered. dIII also binds a well-ordered NADP, but in a different orientation than a classical Rossmann domain.	0
NZ_CP024593.1|WP_088493045.1|2097471_2098578_+|chorismate-synthase	gnl|CDD|376510	pfam01264, Chorismate_synt, Chorismate synthase.	0
NZ_CP024593.1|WP_005875443.1|2084831_2086142_+|pyridoxal-phosphate-dependent-aminotransferase	gnl|CDD|99734	cd00609, AAT_like, Aspartate aminotransferase family. This family belongs to pyridoxal phosphate (PLP)-dependent aspartate aminotransferase superfamily (fold I). Pyridoxal phosphate combines with an alpha-amino acid to form a compound called a Schiff base or aldimine intermediate, which depending on the reaction, is the substrate in four kinds of reactions (1) transamination (movement of amino groups), (2) racemization (redistribution of enantiomers), (3) decarboxylation (removing COOH groups), and (4) various side-chain reactions depending on the enzyme involved. Pyridoxal phosphate (PLP) dependent enzymes were previously classified into alpha, beta and gamma classes, based on the chemical characteristics (carbon atom involved) of the reaction they catalyzed. The availability of several structures allowed a comprehensive analysis of the evolutionary classification of PLP dependent enzymes, and it was found that the functional classification did not always agree with the evolutionary history of these enzymes. The major groups in this CD corresponds to Aspartate aminotransferase a, b and c, Tyrosine, Alanine, Aromatic-amino-acid, Glutamine phenylpyruvate, 1-Aminocyclopropane-1-carboxylate synthase, Histidinol-phosphate, gene products of malY and cobC, Valine-pyruvate aminotransferase and Rhizopine catabolism regulatory protein.	7.51804e-33
NZ_CP024593.1|WP_099811262.1|2086270_2087380_-|hemagglutinin	gnl|CDD|284979	pfam07675, Cleaved_Adhesin, Cleaved Adhesin Domain. This is a family of bacterial protein modules thought to function in various roles including cell adhesion, cell lysis and carbohydrate binding. A tandem repeat of these modules (either two or three repeats) constitute the haemagglutinin/adhesin (HA) regions of the gingipains, RgpA, Kgp, and Lys-gingipain HG66 expressed by Porphyromonas gingivalis (Bacteroides gingivalis). They form components of the major extracellular virulence complex RgpA-Kgp - a mixture of proteinases and adhesin domains. The adhesin domains in this complex are found in proteinase-cleaved forms when isolated from the cell surface. Haemagglutinin genes of P. gingivalis (hagA1 HAGA1_PORGI - and hagA2 HAGA2_PORGI) suggest that such proteins are composed of eight to ten tandem repeats of these adhesin modules. Genomic data predicts that homologous protein modules are also expressed by a number of other bacteria and form part of putative multi-domain proteins. These domains may be acting in concert with other adhesion modules thought to be part of these multi-domain proteins such as fibronectin type III, pfam00041, and Meprin, A5, mu (MAM), pfam00629, domains.	2.55204e-77
NZ_CP024593.1|WP_088442668.1|2077325_2079314_-|NADP-transhydrogenase-subunit-beta	gnl|CDD|376743	pfam02233, PNTB, NAD(P) transhydrogenase beta subunit. This family corresponds to the beta subunit of NADP transhydrogenase in prokaryotes, and either the protein N- or C terminal in eukaryotes. The domain is often found in conjunction with pfam01262. Pyridine nucleotide transhydrogenase catalyzes the reduction of NAD+ to NADPH. A complete loss of activity occurs upon mutation of Gly314 in E. coli.	0
NZ_CP024593.1|WP_077070452.1|2082115_2082370_+|DUF1661-domain-containing-protein	gnl|CDD|285160	pfam07877, DUF1661, Protein of unknown function (DUF1661). This is a family containing bacterial proteins of unknown function. Many of the proteins in this family are hypothetical.	0.000700124
NZ_CP024593.1|WP_004585541.1|2095171_2095738_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	7.66693e-33
NZ_CP024593.1|WP_043895888.1|2082731_2084789_+|acetate--CoA-ligase-family-protein	gnl|CDD|223972	COG1042, COG1042, Acyl-CoA synthetase (NDP forming) [Energy production and conversion].	7.78888e-104

Protein sequences

>NZ_CP024593.1|WP_099811262.1|2086270_2087380_-|hemagglutinin
MKHFNFISLFSALALFFCVQNTLAQQKTEEFAPVSDLRAEAYGSTVFLHWTPPYDNPMIPLSESFESGIPAIWKTIDADGDGYNWMHLTNFTGQSGLCVSSASYIGGVGALTPDNYLITPELKLPTDALVEIIYWVCTQDLTAPSEHYAVYSSSTGNNAADFVNLLYEETLTAKRIQSPELIRGNRTQGIWYQRKVVLPNDTKYVAFRHFNSTDNFWLNLDEVSILYTPLPRRAPCPHPGGYTYSVFRDGQKIASGLSALAYIDTDVPYGTQDYCVQVNYLQGDSYKVCKNIVVANSANIYGADKPFALTVVGKTIVASAIKGEITLYDIRGRLIASSCDTLRYKAENGFYLIKIQVNGTVYTEKIQIQ
>NZ_CP024593.1|WP_005875443.1|2084831_2086142_+|pyridoxal-phosphate-dependent-aminotransferase
MNFPIDEKLIREKQNELHIKDLGMASIRDLVALVTNLEKATGTKFCRMEMGVPGLPAPQIGIETEIQKLREGVASIYPNLDGLPELKQEASRFAKLFVNIDIPARACVPTVGSMQGCFVSFLVANRTHKNREYGTLFIDPGFNLNKLQCRILGQKFESFDLFEYRGEKLREKLESYLQTGQFCSIIYSNPNNPTWQCMTDEELRIIGELATKHDVIVIEDLAYFGMDFRKDYSHPGEPLYQPSVANYTDNYILALSSSKAFSYAGQRIGVLMISGKLYEREYPDLEESFGRLRFGEALSSSALYALSSGATHSAQWGMAAMLKACNDGEYNFRDSVIEYGRKARIMKKMFLDNGFNIVYDKDGNEPLADGFYFTVGYKGMDSSKLIEKFVRYGMCAITLKTTGSKRNEAMRICTSLLPESQFPDLEKRLQMLNAEG
>NZ_CP024593.1|WP_043895888.1|2082731_2084789_+|acetate--CoA-ligase-family-protein
MITPQLIEPRTIAVIGASQDVTKPGGKVLQNILNGSFQGRVLGVNPKVSNVQGVECVPDVKDLPQVDLAILAIPARFCPPTIEVLVKEKGTKGIIVFSAGFSEMGAEGKALERQMAELANEAGATLIGPNCVGVMNPLHQSVFTTPVPVLTPKGCDFISGSGATAVFIMESALSKGLSFSSVYSVGNAAQTGVEDVLEHLDETFDAATSSHTLLLYIETISKPKRFLKHARSLVQKGCRIAAIKSGTSSDGGRAAASHTGAMLNSDVAVDALFRKAGVVRCYSREELATVGAVLQHPVLTGKNMAVITHAGGPAVMLTDALSNGGMSVPPIPEEKTRTLLSELFDGSSVANPIDILATGTAEQLSKVIDTCEKDLDTIDGMVVIFGSPGLFDVSDAYDVIREQQKKCKKPIYAVLPSVINAKEGMERFIAQGGILFEEEVALARAICKVYQTPKPEMTEESELPKAAEIRRLLAGKSGMLGTGDMLQLLDLTGITRPQERLVTTETEALDAARSIGFPLAMKVMGLAHKSDAGGVILNVSTEEGVKESFGKLMQIKGAEGVQVSQMESGVEVFIGVKKEGEFGHLITCGLGGIFVEVMKDIRCALAPLGKNEALEMLRSLKSYPIIRGIRGKQGINDEVIADTLCKISRLLAAVPEIEEMDINPLMGRGERLSAVDVVVRLSDAK
>NZ_CP024593.1|WP_077070452.1|2082115_2082370_+|DUF1661-domain-containing-protein
MYVFGRYLVSSFIGYRGSPPLSSSFCTHINFFCASFYTSAARVFRKRWRKIFFVLARKNFTSRAKSKIFPRHVFRVMNKEIFRT
>NZ_CP024593.1|WP_004585532.1|2081273_2081693_-|large-conductance-mechanosensitive-channel-protein-MscL
MKKFIQDFKAFALKGNVVDMAVGVIIGGAFGKIVTSLVNDIMMPPISLLTGGVNFTDLKLVLSKAVVEGGEVVKPEVSWNYGNFIQTTVDFLILAFVIFLMIKAIMAAKRKEEEAPAAPAPTPPEIELLTEIRDLLKKQ
>NZ_CP024593.1|WP_004585530.1|2079738_2080896_-|Re/Si-specific-NAD(P)(+)-transhydrogenase-subunit-alpha
MIIGIPKEIMHGENRVSATPETVAKFVADGFKVLFEKGAGEGAQYHDEEYAQAGATLVDGAKAVYDGAEVILKVKEPLFNEQLNTHEVELMRKGQYLITFIHPASPVNHEMVRNLAKQGVISLTLDGIPRISRAQNLDALTSMSTCAGYKGILMAAEDFASFIPMMGTAVGMIPPAKVMVIGVGVAGLQALATAKRLGAITYAADIRPAAAEQAQSLGAKIVDTTVPAELAIAEGGYANKLPDDVLAKEREALKATIQDMDIVFCSALIPGKVAPIIITEEMVKGMKRGSVIVDISIDQGGNCEITPKGTKEVKHGVMIQGIKNIPGMLPKSSTWMFAQNMYNLMKYLTKNGRIELDMNDEVCSKILVTRDGEIKHAGTREAMGL
>NZ_CP024593.1|WP_004585529.1|2079310_2079625_-|NAD(P)-transhydrogenase-subunit-alpha
MNPIILIIVLIASTLIGYKLISNVPSLLHTPLMSGMNALSGVTVIGAIAAAGLSFKFGHDGKLILGQIFGGLAIILATINVVGGFGVTHRMLRMFSKKKKGGDQ
>NZ_CP024593.1|WP_088442668.1|2077325_2079314_-|NADP-transhydrogenase-subunit-beta
MSPTIYYILCVLLSLMVLGGISMMSRVKTAVMGNTLSAVAMLGGIILTLVYNEILPAWSVYIFLIIGAGIGWTMAQRVKMIQMPQMVALLNGVGGAASALVGILSLAAIGINPNNNTAADYPIFSQATGMLALTVGMITLVGSLIAAGKLHKLLPQRPVIWPNHSMFTSLLLILTVGFVVLGSVSIEGFPLFWAIIGGLFFSSLFGLFFSIRVGGADMPITISLLNSLSGVAGAIAGMAVGDILLVAVGGIVGASGLLLTQIMCRAMNRKLMSILMASGAKATPAATTPTTASKQEKGEVAAPTPIKAEKTAGSVLRDAKRVIIVPGYGMALAQAQHQVRQLADKLTANGTEVRYAIHPVAGRMPGHMNVLLCEADVPYDQLFEMDAINGDFAQTDAVVVIGANDVMNPAARNAEGTPIYGMPVLNVDDAPEVIICNFDLKPGYAGVDNPLYTRATGVFLKLGDAKESLAEIMKEMDAASDTAATAAPARAEKTAGSVLRDAKRVIIVPGYGMALAQAQHQVRQLADKLTANGTEVRYAIHPVAGRMPGHMNVLLCEADVPYDQLFEMDAINGDFAQTDAVVVIGANDVMNPAARNAEGTPIYGMPVLNVDDAPEVIICNFDLKPGYAGVDNPLYTRATGVFLKLGDAKESLAEIMKEMDIA
>NZ_CP024593.1|WP_004585526.1|2075980_2077180_+|lipid-A-deacylase
MRLSAILIALIVMLPAVLSGQHYYSMAGERPETDSIRPNELSASIRSALFFRNNEYNARSVKGYTLPGARVSAFASYSLPAAHGVKLSLGVSTLNYWGASRYPAGIAYSDLPYWTDYNDYVRLRILPYVQAMLKPTATTALMLGNIAGGTAHGLIEPIYNPELDLTADPEAGVQFRGDWTRFRMDIWVNWMSMIFKNDNHQESFVFGLSTTSKLLSGEGKWRLELPLQAIATHRGGEYNWAQQDTVHTWVNGAVGLKLSYRPRTDKPMQIWGSAYGVAALSSGGYFPYERGWGGYLSLGMDLEHFAFRTDYWYGRHYVSPFAAPFANSLTYDKQPLTNGWGDYIRLYADYSWRMARSVSLAAVARVWFQPSDRFAMSHALELTMRIDPNFPIAFLKDNH
>NZ_CP024593.1|WP_004585525.1|2075003_2075984_+|SPFH/Band-7/PHB-domain-protein
MTATGFILAALIILVIAIIANGLKIVQQSETMIIERLGKYYRTLSSGVSIIIPFIDKPRPIRKRIAYTLPSGQNVVQFKDDTRIDLRETVYDFARQSVITRDNVVTEINAILYFQIVDPMRAMYEISNLPDAIEKLTQTSLRNVIGEMDLDQTLTSRDTINSKLREILDEATNKWGVKVNRVELQDINPPRDIRDAMEKQMRAERDKRAQILQAEGQREALIRESEGKMQESINHAEGEKQAKILRAKAEAEAKILVAKAEAEAIRQISEAVAGSGANPTQYLIAMQYIETLKDINKGDQTKTVYLPFEATGMLGALGGMKDLVKG
>NZ_CP024593.1|WP_004585537.1|2087981_2088551_+|crossover-junction-endodeoxyribonuclease-RuvC
MSPKERIIMGVDPGTILMGYGMLHVVGNTPRLMAMGVIRLEKFDNHYIRLKRIFDRITGLIDEFLPDEMAIEAPFFGKNVQSMLKLGRAQGVAMAAALARDIPITEYAPMRIKQAITGNGNASKEQVAGMLQRYLRIPDEQMLPEMDATDGLAAAVCHFFQTSGPMARSGGSAVKNWKDFVNRNPDKVR
>NZ_CP024593.1|WP_005875438.1|2088598_2089933_-|PhoH-family-protein
MAAKGKKKNFVLDTNVMLHDYECIEKFEENDIYIPIVSLEELDKFKKGSEQINFNARAFVRRLDEISDQDLFAKGASLGEGLGRIFVKINGQYHTKVKEAFGENKADHRILSIAMTLADEQPNIKTILVTKDVNLRMKARSLGMLVEDYINDKVTRVDLFENAEPEYEGVDGDLIDRIYASKDGIDIDEWELGSKIDPNDCFVMKSERNSVLARYNPFTGKIVRVEKGHYFGIQPRNAEQTFAMHILTDPNVKLIGLTGKAGTGKTLLALAAALSQEQSYKQILLARPIVSLANKDLGFLPGDEKAKVAPYMQPLFDNLNVIKGQLAQNSSELRRLDEMQKTEKLVIEALAYIRGRSVSETIFIVDEAQNLTPHEIKTIITRAGEGSKLIFTGDIEQIDSPYLDAQSNGLAYMIERMKGQPLFAHVNLIKGERSELSELASDLL
>NZ_CP024593.1|WP_004585540.1|2090089_2091757_+|formate--tetrahydrofolate-ligase
MKSDIQIARDIELQRIEQIAESIDLPVEQLEPYGRYTAKVPLSCIDEEKVKKGNLILVTAITPNKAGVGKTTVSIGLALGLNHIGKKAIVALREPSLGPCFGMKGGAAGGGYAQVLPMENINLHFTGDFHAVTSAHNMITALLENYIYQNRNTCDGLSEILWKRVLDVNDRSLRNAVTGLGTISDGIPRQTGFDITPASEIMAILCLAKDFEDLRSRLENILLGYTKEGAPFTVKDLGIAGSIAVLLKDAIKPNLVQTTEHTPAFVHGGPFANIAHGCNSILATKMALSFGEYAVTEAGFGADLGAEKFLDIKCREMGVAPKLTVLVATLRALKLHGGVAETEIKAPNAEALRRGLSNLDRHIYNLKKFGQQVIVAFNRFDTDEEEEISIVREHCIGQNVGFAVNNAFAEGGKGAEELAKLVVEMVENKPSQPLKYAYEPENPVKMKIEKIAKEIYSAGSVVYSSKADGKLKKIAMQSLDHLPVCIAKTQYSFSSDPKAKGDVRGFELKVSDIIINRGAGMLVVIIGEIMRMPGLPKEPQAVHIDIVDGFIEGLS
>NZ_CP024593.1|WP_043889970.1|2092677_2093580_-|IS982-like-element-IS195-family-transposase
MKTNIVDVFCIIDDFSKLFDETIKKKTLEEADKKRRNRKFKMSDSEVMTILILFHLSRYRDLKAFYLQYITHSCRSEFPHLVSYNRFVELQSRVGFKLIAFLNMCCLGQCTGISFIDSTPLKACHIKRAHGHRTMRGWAQKGKSTMGWFYGFKLHIVINDRGEIINYQITPGNCDDREPLKDGTFTKNLFGKLIADRGYISQNLFDRLFVDDIHMITKIKKNMKNSLMHLYDKVLLRKRALIETVNDMLKNVCRIEHTRHRSVNNFVTNLISGIIAYNILPKKPELNIEIIRNPNFPISA
>NZ_CP024593.1|WP_023847284.1|2094862_2095024_-|hypothetical-protein
MRQSKFKSFAVALLRQGIANASRLLPKIRAKKVFNNEAEFGMILNKGVKRSGF
>NZ_CP024593.1|WP_004585541.1|2095171_2095738_+|sigma-70-family-RNA-polymerase-sigma-factor
MADKLLISEEELLEELRDPARRRMAFEKVVRLYNRKLYWQIRRMVLSHDDTDDLLQNTFMKAWSALDGFRGEAKLSTWLYRIAMYESLNFLKKKKIEDDMSISITDENSYLLDNLTGDVYFDGDEAEIAFQKAILELPDKQRLVFNLRYYDEMPYEKMAEITGTSEGALKASYHHAVKKLERFLSPDD
>NZ_CP024593.1|WP_099811848.1|2095785_2096196_+|hypothetical-protein
MKQFDPDVNIRPKEDSIRHYSVPDDYFVSFTDKLMAQIPAVKEENTVVVPSVALWPKLRPLLYLAASFLLMIGMFKAFSLFGEGSDTGRTTSTSAGLVALDHGDTRWSEDTDYRDFLHDNCAETVSDEWVLTDFSE
>NZ_CP024593.1|WP_005873416.1|2096168_2096699_+|hypothetical-protein
MGTNGFQRMIERHSHHHLSGMKRIFSLTIILAALLPTLSQAAMPPYSVATKFQESEQQGRKREFMNQRNAFFILELELTQEETDAFLPLYNELDTKRYELWKDVRQKRALMERKAELTDADMELIINKSLDNKIAEARLEKEYYYKFKRVLPMRKVMALKVAERKFARLFLKSSYD
>NZ_CP024593.1|WP_012458032.1|2096749_2097322_+|peptidylprolyl-isomerase
MSISANKFVTCSYDLYVGLAEEKELMEQATAERPLCYIHGMGMMLPEFEKHLFGLAVGDKFDFELKSEDAYGERQEDAVLELPKDIFKDEEGRFDSSIVYEGNTVPMRDAEGNTLQGSVLEVRDDVVVMDFNHPLAGENLHFIGEIIEEREATAEEIEQFFGGHSGCGCGCSCESESSDGCSCGSDCGCH
>NZ_CP024593.1|WP_088493045.1|2097471_2098578_+|chorismate-synthase
MNTIGKLFRLTTFGESHGKAIGGVIDGCPAGLFVDMEAIERELLRRRPGQSHYTSPRQESDMVQFISGLFRGETTGAPIAFMIDNKDVRSADYDSLSSIFRPGHADYTYFHKYGIRDTRGGGRSSARETAVRVVAGAVAKQLLAPLGIRCTAYTSQIGPVCIPQENAKEYSPEEVESSPIRCPDPNASGLMEAVIETAKKESDSVGGIVDCHISGVPVGWGEPLYGKLHAALGAAMLSINAAKGFEVGDGFALASMRGSEANDQMVAAEDGGISFLSNHSGGISGGISTGQDIRFRVAFKPTPTIGQKQQTVNEQGESISLSAVGRHDPCVVPRAVPVVEAMTWLTLADAYLASRSGRCAHSSLKCNG

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP024593_9	9.1|2087914|33|NZ_CP024593|CRISPRCasFinder	2087914-2087946	33	NZ_CP024593.1	1080430-1080462	1	0.97

1. spacer 9.1|2087914|33|NZ_CP024593|CRISPRCasFinder matches to position: 1080430-1080462, mismatch: 1, identity: 0.97

tcctccacgatctcggtgtctgatctgcttttt	CRISPR spacer
tcctccacgacctcggtgtctgatctgcttttt	Protospacer
**********.**********************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP024593_6	6.64|1083783|23|NZ_CP024593|CRT	1083783-1083805	23	NZ_CP024986	Streptomyces lavendulae subsp. lavendulae strain CCM 3239 plasmid pSA3239, complete sequence	193351-193373	3	0.87
NZ_CP024593_6	6.64|1083783|23|NZ_CP024593|CRT	1083783-1083805	23	NC_024970	Streptomyces aureofaciens strain CCM3239 plasmid pSA3239, complete sequence	47704-47726	3	0.87
NZ_CP024593_6	6.64|1083783|23|NZ_CP024593|CRT	1083783-1083805	23	NZ_KJ396772	Streptomyces lavendulae subsp. lavendulae strain CCM3239 plasmid pSA3239, complete sequence	47704-47726	3	0.87
NZ_CP024593_3	3.4|739763|29|NZ_CP024593|PILER-CR,CRT	739763-739791	29	NC_014249	'Nostoc azollae' 0708 plasmid pAzo01, complete sequence	89231-89259	5	0.828
NZ_CP024593_3	3.9|739762|30|NZ_CP024593|CRISPRCasFinder	739762-739791	30	NC_014249	'Nostoc azollae' 0708 plasmid pAzo01, complete sequence	89230-89259	5	0.833
NZ_CP024593_3	3.2|739631|29|NZ_CP024593|PILER-CR,CRT	739631-739659	29	NZ_LR594660	Variovorax sp. PBL-H6 plasmid 2	702287-702315	6	0.793
NZ_CP024593_3	3.2|739631|29|NZ_CP024593|PILER-CR,CRT	739631-739659	29	NZ_LR594667	Variovorax sp. SRS16 plasmid 2	135874-135902	6	0.793
NZ_CP024593_3	3.2|739631|29|NZ_CP024593|PILER-CR,CRT	739631-739659	29	NZ_LR594672	Variovorax sp. PBL-E5 plasmid 2	135874-135902	6	0.793
NZ_CP024593_3	3.4|739763|29|NZ_CP024593|PILER-CR,CRT	739763-739791	29	NC_029119	Staphylococcus phage SPbeta-like, complete genome	14077-14105	6	0.793
NZ_CP024593_3	3.9|739762|30|NZ_CP024593|CRISPRCasFinder	739762-739791	30	NZ_CP045304	Legionella longbeachae strain B1445CHC plasmid pB1445CHC_73K, complete sequence	35618-35647	6	0.8
NZ_CP024593_3	3.9|739762|30|NZ_CP024593|CRISPRCasFinder	739762-739791	30	NZ_CP045307	Legionella longbeachae strain B41211CHC plasmid pB41211CHC_76k, complete sequence	35596-35625	6	0.8
NZ_CP024593_3	3.9|739762|30|NZ_CP024593|CRISPRCasFinder	739762-739791	30	NC_014544	Legionella longbeachae NSW150 plasmid pLLO, complete sequence	35926-35955	6	0.8
NZ_CP024593_3	3.9|739762|30|NZ_CP024593|CRISPRCasFinder	739762-739791	30	NZ_CP025493	Legionella sainthelensi strain LA01-117 plasmid pLA01-117_113k, complete sequence	7714-7743	6	0.8
NZ_CP024593_3	3.2|739631|29|NZ_CP024593|PILER-CR,CRT	739631-739659	29	NZ_LR594690	Variovorax sp. WDL1 plasmid 2	135472-135500	7	0.759
NZ_CP024593_3	3.3|739697|29|NZ_CP024593|PILER-CR,CRT	739697-739725	29	NZ_LT907976	Pseudodesulfovibrio profundus strain 500-1 plasmid paDPRO, complete sequence	15253-15281	7	0.759
NZ_CP024593_3	3.5|739829|29|NZ_CP024593|PILER-CR,CRT	739829-739857	29	NZ_CP012478	Arthrobacter sp. ERGS1:01 isolate water plasmid unnamed1, complete sequence	25258-25286	7	0.759
NZ_CP024593_3	3.7|739630|30|NZ_CP024593|CRISPRCasFinder	739630-739659	30	NZ_LR594660	Variovorax sp. PBL-H6 plasmid 2	702286-702315	7	0.767
NZ_CP024593_3	3.7|739630|30|NZ_CP024593|CRISPRCasFinder	739630-739659	30	NZ_LR594667	Variovorax sp. SRS16 plasmid 2	135874-135903	7	0.767
NZ_CP024593_3	3.7|739630|30|NZ_CP024593|CRISPRCasFinder	739630-739659	30	NZ_LR594672	Variovorax sp. PBL-E5 plasmid 2	135874-135903	7	0.767
NZ_CP024593_3	3.8|739696|30|NZ_CP024593|CRISPRCasFinder	739696-739725	30	NZ_LT907976	Pseudodesulfovibrio profundus strain 500-1 plasmid paDPRO, complete sequence	15253-15282	7	0.767
NZ_CP024593_3	3.9|739762|30|NZ_CP024593|CRISPRCasFinder	739762-739791	30	NC_029119	Staphylococcus phage SPbeta-like, complete genome	14077-14106	7	0.767
NZ_CP024593_6	6.48|1085103|34|NZ_CP024593|PILER-CR,CRISPRCasFinder	1085103-1085136	34	HQ634191	Cyanophage Syn10 genomic sequence	131659-131692	7	0.794
NZ_CP024593_6	6.48|1085103|34|NZ_CP024593|PILER-CR,CRISPRCasFinder	1085103-1085136	34	DQ149023	Synechococcus cyanophage syn9, complete genome	17920-17953	7	0.794
NZ_CP024593_6	6.48|1085103|34|NZ_CP024593|PILER-CR,CRISPRCasFinder	1085103-1085136	34	NC_008296	Synechococcus phage syn9, complete genome	17920-17953	7	0.794
NZ_CP024593_6	6.98|1088047|34|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder	1088047-1088080	34	NZ_LN831028	Fusobacterium nucleatum subsp. polymorphum strain NCTC10562 plasmid 2, complete sequence	1934-1967	7	0.794
NZ_CP024593_3	3.3|739697|29|NZ_CP024593|PILER-CR,CRT	739697-739725	29	MF479730	Aeromonas phage AS-gz, complete genome	103640-103668	8	0.724
NZ_CP024593_3	3.7|739630|30|NZ_CP024593|CRISPRCasFinder	739630-739659	30	NZ_LR594690	Variovorax sp. WDL1 plasmid 2	135472-135501	8	0.733
NZ_CP024593_3	3.10|739828|30|NZ_CP024593|CRISPRCasFinder	739828-739857	30	NZ_CP012478	Arthrobacter sp. ERGS1:01 isolate water plasmid unnamed1, complete sequence	25258-25287	8	0.733
NZ_CP024593_6	6.9|1082531|34|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT	1082531-1082564	34	NZ_CP021355	Rhodococcus sp. S2-17 plasmid pRB98, complete sequence	875765-875798	8	0.765
NZ_CP024593_6	6.37|1084378|35|NZ_CP024593|PILER-CR,CRISPRCasFinder	1084378-1084412	35	NZ_CP030074	Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence	400465-400499	8	0.771
NZ_CP024593_6	6.38|1084443|35|NZ_CP024593|PILER-CR,CRISPRCasFinder	1084443-1084477	35	NZ_CP030074	Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence	400465-400499	8	0.771
NZ_CP024593_6	6.88|1087387|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder	1087387-1087423	37	CP006880	Rhizobium gallicum bv. gallicum R602 plasmid pRgalR602c, complete sequence	2273933-2273969	8	0.784
NZ_CP024593_6	6.98|1088047|34|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder	1088047-1088080	34	NZ_LN831028	Fusobacterium nucleatum subsp. polymorphum strain NCTC10562 plasmid 2, complete sequence	5679-5712	8	0.765
NZ_CP024593_9	9.1|2087914|33|NZ_CP024593|CRISPRCasFinder	2087914-2087946	33	NZ_CP016459	Blastomonas sp. RAC04 plasmid pBSY18_3, complete sequence	18073-18105	8	0.758
NZ_CP024593_3	3.4|739763|29|NZ_CP024593|PILER-CR,CRT	739763-739791	29	MK893987	Staphylococcus phage PMBT8, complete genome	79385-79413	9	0.69
NZ_CP024593_3	3.8|739696|30|NZ_CP024593|CRISPRCasFinder	739696-739725	30	MF479730	Aeromonas phage AS-gz, complete genome	103640-103669	9	0.7
NZ_CP024593_3	3.9|739762|30|NZ_CP024593|CRISPRCasFinder	739762-739791	30	MK893987	Staphylococcus phage PMBT8, complete genome	79385-79414	9	0.7
NZ_CP024593_6	6.82|1086992|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder	1086992-1087026	35	MN698248	Pelagibacter phage HTVC202P, complete genome	24879-24913	9	0.743
NZ_CP024593_6	6.87|1087320|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder	1087320-1087356	37	AP014148	Uncultured Mediterranean phage uvMED isolate uvMED-GF-C4B-MedDCM-OCT-S32-C91, *** SEQUENCING IN PROGRESS ***	28819-28855	9	0.757
NZ_CP024593_6	6.87|1087320|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder	1087320-1087356	37	AP014143	Uncultured Mediterranean phage uvMED isolate uvMED-GF-C4B-MedDCM-OCT-S24-C76, *** SEQUENCING IN PROGRESS ***	1468-1504	9	0.757
NZ_CP024593_6	6.87|1087320|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder	1087320-1087356	37	AP014144	Uncultured Mediterranean phage uvMED isolate uvMED-GF-C4B-MedDCM-OCT-S25-C77, *** SEQUENCING IN PROGRESS ***	1468-1504	9	0.757
NZ_CP024593_6	6.87|1087320|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder	1087320-1087356	37	AP014147	Uncultured Mediterranean phage uvMED isolate uvMED-GF-C4B-MedDCM-OCT-S30-C164, *** SEQUENCING IN PROGRESS ***	1468-1504	9	0.757
NZ_CP024593_6	6.88|1087387|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder	1087387-1087423	37	NZ_CP017105	Rhizobium gallicum strain IE4872 plasmid pRgalIE4872d, complete sequence	2186285-2186321	9	0.757
NZ_CP024593_6	6.88|1087387|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder	1087387-1087423	37	NZ_CP017244	Rhizobium etli 8C-3 plasmid pRsp8C3c, complete sequence	279230-279266	9	0.757
NZ_CP024593_6	6.137|1090619|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder	1090619-1090654	36	NZ_CP045296	Paenibacillus cellulositrophicus strain KACC 16577 plasmid unnamed1, complete sequence	138548-138583	9	0.75
NZ_CP024593_6	6.9|1082531|34|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT	1082531-1082564	34	NZ_CP030127	Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence	578532-578565	10	0.706
NZ_CP024593_6	6.48|1085103|34|NZ_CP024593|PILER-CR,CRISPRCasFinder	1085103-1085136	34	KJ803031	Dinoroseobacter phage vBDshPR2C, complete genome	5950-5983	10	0.706
NZ_CP024593_6	6.98|1088047|34|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder	1088047-1088080	34	NC_014628	Paenibacillus polymyxa SC2 plasmid pSC2, complete sequence	217081-217114	10	0.706
NZ_CP024593_6	6.48|1085103|34|NZ_CP024593|PILER-CR,CRISPRCasFinder	1085103-1085136	34	KJ621082	Dinoroseobacter phage DFL12phi1, complete genome	68119-68152	11	0.676
NZ_CP024593_6	6.108|1088712|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder	1088712-1088747	36	NZ_CP010990	Pseudonocardia sp. EC080625-04 plasmid pFRP1-1, complete sequence	96334-96369	12	0.667

1. spacer 6.64|1083783|23|NZ_CP024593|CRT matches to NZ_CP024986 (Streptomyces lavendulae subsp. lavendulae strain CCM 3239 plasmid pSA3239, complete sequence) position: , mismatch: 3, identity: 0.87

gctgatatcccccaccagcagca	CRISPR spacer
cctgatgtcccccaccagcagct	Protospacer
 *****.*************** 

2. spacer 6.64|1083783|23|NZ_CP024593|CRT matches to NC_024970 (Streptomyces aureofaciens strain CCM3239 plasmid pSA3239, complete sequence) position: , mismatch: 3, identity: 0.87

gctgatatcccccaccagcagca	CRISPR spacer
cctgatgtcccccaccagcagct	Protospacer
 *****.*************** 

3. spacer 6.64|1083783|23|NZ_CP024593|CRT matches to NZ_KJ396772 (Streptomyces lavendulae subsp. lavendulae strain CCM3239 plasmid pSA3239, complete sequence) position: , mismatch: 3, identity: 0.87

gctgatatcccccaccagcagca	CRISPR spacer
cctgatgtcccccaccagcagct	Protospacer
 *****.*************** 

4. spacer 3.4|739763|29|NZ_CP024593|PILER-CR,CRT matches to NC_014249 ('Nostoc azollae' 0708 plasmid pAzo01, complete sequence) position: , mismatch: 5, identity: 0.828

tataaaagccactgaaaaatatgtaaaag	CRISPR spacer
tataaaagtcactgaaaaataagtaagtc	Protospacer
********.************ ****.  

5. spacer 3.9|739762|30|NZ_CP024593|CRISPRCasFinder matches to NC_014249 ('Nostoc azollae' 0708 plasmid pAzo01, complete sequence) position: , mismatch: 5, identity: 0.833

ttataaaagccactgaaaaatatgtaaaag	CRISPR spacer
ttataaaagtcactgaaaaataagtaagtc	Protospacer
*********.************ ****.  

6. spacer 3.2|739631|29|NZ_CP024593|PILER-CR,CRT matches to NZ_LR594660 (Variovorax sp. PBL-H6 plasmid 2) position: , mismatch: 6, identity: 0.793

ttctgaagacatgtttatcgacgtcgtag	CRISPR spacer
tgtaaaagacatgttcatcgacggcgtag	Protospacer
* . .**********.******* *****

7. spacer 3.2|739631|29|NZ_CP024593|PILER-CR,CRT matches to NZ_LR594667 (Variovorax sp. SRS16 plasmid 2) position: , mismatch: 6, identity: 0.793

ttctgaagacatgtttatcgacgtcgtag	CRISPR spacer
tgtaaaagacatgttcatcgacggcgtag	Protospacer
* . .**********.******* *****

8. spacer 3.2|739631|29|NZ_CP024593|PILER-CR,CRT matches to NZ_LR594672 (Variovorax sp. PBL-E5 plasmid 2) position: , mismatch: 6, identity: 0.793

ttctgaagacatgtttatcgacgtcgtag	CRISPR spacer
tgtaaaagacatgttcatcgacggcgtag	Protospacer
* . .**********.******* *****

9. spacer 3.4|739763|29|NZ_CP024593|PILER-CR,CRT matches to NC_029119 (Staphylococcus phage SPbeta-like, complete genome) position: , mismatch: 6, identity: 0.793

tataaaagccactgaaaaatatgtaaaag	CRISPR spacer
tataaaagccattaaaaaatatgtgtata	Protospacer
***********.*.**********. * .

10. spacer 3.9|739762|30|NZ_CP024593|CRISPRCasFinder matches to NZ_CP045304 (Legionella longbeachae strain B1445CHC plasmid pB1445CHC_73K, complete sequence) position: , mismatch: 6, identity: 0.8

ttataaaagccactgaaaaatatgtaaaag-	CRISPR spacer
ttataaaagccgctgaaaaat-tatatgact	Protospacer
***********.********* *.** .*  

11. spacer 3.9|739762|30|NZ_CP024593|CRISPRCasFinder matches to NZ_CP045307 (Legionella longbeachae strain B41211CHC plasmid pB41211CHC_76k, complete sequence) position: , mismatch: 6, identity: 0.8

ttataaaagccactgaaaaatatgtaaaag---	CRISPR spacer
ttataaaagccgctgaaaaat---tacatgact	Protospacer
***********.*********   ** * *   

12. spacer 3.9|739762|30|NZ_CP024593|CRISPRCasFinder matches to NC_014544 (Legionella longbeachae NSW150 plasmid pLLO, complete sequence) position: , mismatch: 6, identity: 0.8

ttataaaagccactgaaaaatatgtaaaag---	CRISPR spacer
ttataaaagccgctgaaaaat---tacatgact	Protospacer
***********.*********   ** * *   

13. spacer 3.9|739762|30|NZ_CP024593|CRISPRCasFinder matches to NZ_CP025493 (Legionella sainthelensi strain LA01-117 plasmid pLA01-117_113k, complete sequence) position: , mismatch: 6, identity: 0.8

ttataaaagccactgaaaaatatgtaaaag-	CRISPR spacer
ttataaaagccgctgaaaaat-tacataact	Protospacer
***********.********* *..* **  

14. spacer 3.2|739631|29|NZ_CP024593|PILER-CR,CRT matches to NZ_LR594690 (Variovorax sp. WDL1 plasmid 2) position: , mismatch: 7, identity: 0.759

ttctgaagacatgtttatcgacgtcgtag	CRISPR spacer
cgtaaaagacatgttcatcgacggcgtag	Protospacer
. . .**********.******* *****

15. spacer 3.3|739697|29|NZ_CP024593|PILER-CR,CRT matches to NZ_LT907976 (Pseudodesulfovibrio profundus strain 500-1 plasmid paDPRO, complete sequence) position: , mismatch: 7, identity: 0.759

ttattggtgatgataaacaacttcctcct	CRISPR spacer
cgctgagtgatgataaacaatttccacct	Protospacer
.  * .**************.**** ***

16. spacer 3.5|739829|29|NZ_CP024593|PILER-CR,CRT matches to NZ_CP012478 (Arthrobacter sp. ERGS1:01 isolate water plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.759

gatggacgatgatacggcctatttcggtt	CRISPR spacer
cttggacgatgatgcggcctctttccgcc	Protospacer
  ***********.****** **** *..

17. spacer 3.7|739630|30|NZ_CP024593|CRISPRCasFinder matches to NZ_LR594660 (Variovorax sp. PBL-H6 plasmid 2) position: , mismatch: 7, identity: 0.767

cttctgaagacatgtttatcgacgtcgtag	CRISPR spacer
ttgtaaaagacatgttcatcgacggcgtag	Protospacer
.* . .**********.******* *****

18. spacer 3.7|739630|30|NZ_CP024593|CRISPRCasFinder matches to NZ_LR594667 (Variovorax sp. SRS16 plasmid 2) position: , mismatch: 7, identity: 0.767

cttctgaagacatgtttatcgacgtcgtag	CRISPR spacer
ttgtaaaagacatgttcatcgacggcgtag	Protospacer
.* . .**********.******* *****

19. spacer 3.7|739630|30|NZ_CP024593|CRISPRCasFinder matches to NZ_LR594672 (Variovorax sp. PBL-E5 plasmid 2) position: , mismatch: 7, identity: 0.767

cttctgaagacatgtttatcgacgtcgtag	CRISPR spacer
ttgtaaaagacatgttcatcgacggcgtag	Protospacer
.* . .**********.******* *****

20. spacer 3.8|739696|30|NZ_CP024593|CRISPRCasFinder matches to NZ_LT907976 (Pseudodesulfovibrio profundus strain 500-1 plasmid paDPRO, complete sequence) position: , mismatch: 7, identity: 0.767

tttattggtgatgataaacaacttcctcct	CRISPR spacer
tcgctgagtgatgataaacaatttccacct	Protospacer
*.  * .**************.**** ***

21. spacer 3.9|739762|30|NZ_CP024593|CRISPRCasFinder matches to NC_029119 (Staphylococcus phage SPbeta-like, complete genome) position: , mismatch: 7, identity: 0.767

ttataaaagccactgaaaaatatgtaaaag	CRISPR spacer
ctataaaagccattaaaaaatatgtgtata	Protospacer
.***********.*.**********. * .

22. spacer 6.48|1085103|34|NZ_CP024593|PILER-CR,CRISPRCasFinder matches to HQ634191 (Cyanophage Syn10 genomic sequence) position: , mismatch: 7, identity: 0.794

--accaagatgtcaagaagtccatcatgatgattgt	CRISPR spacer
taaccata--ctcaagaagtccatggtgatgattgt	Protospacer
  **** .   ************* .**********

23. spacer 6.48|1085103|34|NZ_CP024593|PILER-CR,CRISPRCasFinder matches to DQ149023 (Synechococcus cyanophage syn9, complete genome) position: , mismatch: 7, identity: 0.794

--accaagatgtcaagaagtccatcatgatgattgt	CRISPR spacer
taaccata--ctcaagaagtccatggtgatgattgt	Protospacer
  **** .   ************* .**********

24. spacer 6.48|1085103|34|NZ_CP024593|PILER-CR,CRISPRCasFinder matches to NC_008296 (Synechococcus phage syn9, complete genome) position: , mismatch: 7, identity: 0.794

--accaagatgtcaagaagtccatcatgatgattgt	CRISPR spacer
taaccata--ctcaagaagtccatggtgatgattgt	Protospacer
  **** .   ************* .**********

25. spacer 6.98|1088047|34|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder matches to NZ_LN831028 (Fusobacterium nucleatum subsp. polymorphum strain NCTC10562 plasmid 2, complete sequence) position: , mismatch: 7, identity: 0.794

taaaacaaaaaattttagagattatgttacgatc	CRISPR spacer
taaaacaaaaaaatttagatattataaaactatt	Protospacer
************ ****** *****.  ** **.

26. spacer 3.3|739697|29|NZ_CP024593|PILER-CR,CRT matches to MF479730 (Aeromonas phage AS-gz, complete genome) position: , mismatch: 8, identity: 0.724

ttattggtgatgataaacaacttcctcct	CRISPR spacer
ttatgggtgatgatgaacaacttaacgag	Protospacer
**** *********.********  .   

27. spacer 3.7|739630|30|NZ_CP024593|CRISPRCasFinder matches to NZ_LR594690 (Variovorax sp. WDL1 plasmid 2) position: , mismatch: 8, identity: 0.733

cttctgaagacatgtttatcgacgtcgtag	CRISPR spacer
tcgtaaaagacatgttcatcgacggcgtag	Protospacer
.. . .**********.******* *****

28. spacer 3.10|739828|30|NZ_CP024593|CRISPRCasFinder matches to NZ_CP012478 (Arthrobacter sp. ERGS1:01 isolate water plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.733

tgatggacgatgatacggcctatttcggtt	CRISPR spacer
acttggacgatgatgcggcctctttccgcc	Protospacer
   ***********.****** **** *..

29. spacer 6.9|1082531|34|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021355 (Rhodococcus sp. S2-17 plasmid pRB98, complete sequence) position: , mismatch: 8, identity: 0.765

gagcctcgatgcatcccgaggcggaagccagcct	CRISPR spacer
aagcctcgattcatcgcgaggcggaagggcgggt	Protospacer
.********* **** ***********   *  *

30. spacer 6.37|1084378|35|NZ_CP024593|PILER-CR,CRISPRCasFinder matches to NZ_CP030074 (Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.771

gcac-ctcttcgggatcgagcaccccgtcttcgcga	CRISPR spacer
-cgcggtctccgggatcgagcaccacgtcttcgtcg	Protospacer
 *.*  ***.************** ********. .

31. spacer 6.38|1084443|35|NZ_CP024593|PILER-CR,CRISPRCasFinder matches to NZ_CP030074 (Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.771

gcac-ctcttcgggatcgagcaccccgtcttcgcga	CRISPR spacer
-cgcggtctccgggatcgagcaccacgtcttcgtcg	Protospacer
 *.*  ***.************** ********. .

32. spacer 6.88|1087387|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder matches to CP006880 (Rhizobium gallicum bv. gallicum R602 plasmid pRgalR602c, complete sequence) position: , mismatch: 8, identity: 0.784

ccctcgagccgggcgcaacggttgccgatgccagaaa	CRISPR spacer
gggtcgagccgggcgcaacgcttgccgatgtcgataa	Protospacer
   ***************** *********.*.. **

33. spacer 6.98|1088047|34|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder matches to NZ_LN831028 (Fusobacterium nucleatum subsp. polymorphum strain NCTC10562 plasmid 2, complete sequence) position: , mismatch: 8, identity: 0.765

taaaacaaaaaattttagagattatgttacgatc	CRISPR spacer
taaaacaaaaaaatttagatattataaaactact	Protospacer
************ ****** *****.  ** *..

34. spacer 9.1|2087914|33|NZ_CP024593|CRISPRCasFinder matches to NZ_CP016459 (Blastomonas sp. RAC04 plasmid pBSY18_3, complete sequence) position: , mismatch: 8, identity: 0.758

tcctccacgatctcggtgtctgatctgcttttt	CRISPR spacer
tgttccgcgatctgggtgtctgatctgcagggt	Protospacer
* .***.****** **************    *

35. spacer 3.4|739763|29|NZ_CP024593|PILER-CR,CRT matches to MK893987 (Staphylococcus phage PMBT8, complete genome) position: , mismatch: 9, identity: 0.69

tataaaagccactgaaaaatatgtaaaag	CRISPR spacer
agacaaagccacagaaaaatatgtagtta	Protospacer
 .  ******** ************.  .

36. spacer 3.8|739696|30|NZ_CP024593|CRISPRCasFinder matches to MF479730 (Aeromonas phage AS-gz, complete genome) position: , mismatch: 9, identity: 0.7

tttattggtgatgataaacaacttcctcct	CRISPR spacer
cttatgggtgatgatgaacaacttaacgag	Protospacer
.**** *********.********  .   

37. spacer 3.9|739762|30|NZ_CP024593|CRISPRCasFinder matches to MK893987 (Staphylococcus phage PMBT8, complete genome) position: , mismatch: 9, identity: 0.7

ttataaaagccactgaaaaatatgtaaaag	CRISPR spacer
tagacaaagccacagaaaaatatgtagtta	Protospacer
* .  ******** ************.  .

38. spacer 6.82|1086992|35|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder matches to MN698248 (Pelagibacter phage HTVC202P, complete genome) position: , mismatch: 9, identity: 0.743

atggaaatgctattgcagattgtac-----agatactatt	CRISPR spacer
atggaaatgctattggagatggtactttagaatta-----	Protospacer
*************** **** ****     *. **     

39. spacer 6.87|1087320|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder matches to AP014148 (Uncultured Mediterranean phage uvMED isolate uvMED-GF-C4B-MedDCM-OCT-S32-C91, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 9, identity: 0.757

tagttacaaaacataaacaagaaaaaagaattttcat	CRISPR spacer
tagttaaaatacataaacaagaaaaagatatagcaat	Protospacer
****** ** ****************.. **  . **

40. spacer 6.87|1087320|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder matches to AP014143 (Uncultured Mediterranean phage uvMED isolate uvMED-GF-C4B-MedDCM-OCT-S24-C76, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 9, identity: 0.757

tagttacaaaacataaacaagaaaaaagaattttcat	CRISPR spacer
tagttaaaatacataaacaagaaaaagatatagcaat	Protospacer
****** ** ****************.. **  . **

41. spacer 6.87|1087320|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder matches to AP014144 (Uncultured Mediterranean phage uvMED isolate uvMED-GF-C4B-MedDCM-OCT-S25-C77, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 9, identity: 0.757

tagttacaaaacataaacaagaaaaaagaattttcat	CRISPR spacer
tagttaaaatacataaacaagaaaaagatatagcaat	Protospacer
****** ** ****************.. **  . **

42. spacer 6.87|1087320|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder matches to AP014147 (Uncultured Mediterranean phage uvMED isolate uvMED-GF-C4B-MedDCM-OCT-S30-C164, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 9, identity: 0.757

tagttacaaaacataaacaagaaaaaagaattttcat	CRISPR spacer
tagttaaaatacataaacaagaaaaagatatagcaat	Protospacer
****** ** ****************.. **  . **

43. spacer 6.88|1087387|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP017105 (Rhizobium gallicum strain IE4872 plasmid pRgalIE4872d, complete sequence) position: , mismatch: 9, identity: 0.757

ccctcgagccgggcgcaacggttgccgatgccagaaa	CRISPR spacer
gggtcgagccgggcgcaacgcttgctgatgtcgataa	Protospacer
   ***************** ****.****.*.. **

44. spacer 6.88|1087387|37|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP017244 (Rhizobium etli 8C-3 plasmid pRsp8C3c, complete sequence) position: , mismatch: 9, identity: 0.757

ccctcgagccgggcgcaacggttgccgatgccagaaa	CRISPR spacer
gggtcgagccgggcgcaacgcttgctgatgtcgataa	Protospacer
   ***************** ****.****.*.. **

45. spacer 6.137|1090619|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP045296 (Paenibacillus cellulositrophicus strain KACC 16577 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.75

gacgtgcagctggagatcgaggaaaacaccgccttg	CRISPR spacer
gacgtgaagctggagatcgtggaaaaaggctcgcag	Protospacer
****** ************ ****** . * * . *

46. spacer 6.9|1082531|34|NZ_CP024593|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP030127 (Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.706

gagcctcgatgcatcccgaggcggaagccagcct	CRISPR spacer
tcccctcggtgcatcccgaggctgaaggccgggc	Protospacer
   *****.************* **** * *  .

47. spacer 6.48|1085103|34|NZ_CP024593|PILER-CR,CRISPRCasFinder matches to KJ803031 (Dinoroseobacter phage vBDshPR2C, complete genome) position: , mismatch: 10, identity: 0.706

accaagatgtcaagaagtccatcatgatgattgt	CRISPR spacer
gaaaagatgtgaagcagtccatcatgactgctct	Protospacer
.  ******* *** ************. ..* *

48. spacer 6.98|1088047|34|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder matches to NC_014628 (Paenibacillus polymyxa SC2 plasmid pSC2, complete sequence) position: , mismatch: 10, identity: 0.706

taaaacaaaaaattttagagattatgttacgatc	CRISPR spacer
caaaacataaaaatttagagattatacaccacta	Protospacer
.****** **** ************..  *. * 

49. spacer 6.48|1085103|34|NZ_CP024593|PILER-CR,CRISPRCasFinder matches to KJ621082 (Dinoroseobacter phage DFL12phi1, complete genome) position: , mismatch: 11, identity: 0.676

accaagatgtcaagaagtccatcatgatgattgt	CRISPR spacer
ggaaagatgtgaagcagtccatcatgactgcact	Protospacer
.  ******* *** ************. ..  *

50. spacer 6.108|1088712|36|NZ_CP024593|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP010990 (Pseudonocardia sp. EC080625-04 plasmid pFRP1-1, complete sequence) position: , mismatch: 12, identity: 0.667

tatttaacgacgaggacggcgtgcgcaaggcggagc	CRISPR spacer
cccaccacgacgaggtcggcgtgctcaaggcgcccg	Protospacer
. . . ********* ******** *******    

Anti-CRISPR protein detection

Acr ID	Acr position	Acr size	Homology with known anti	Neighbor HTH/AcRanker	Neighbor Aca	In prophage	Protospacer in prophage
NZ_CP024593.1|WP_039417454.1|167175_167598_+|PcfK-like-protein	167175_167598_+	140 aa aa	40	NA	NA	No	NA
NZ_CP024593.1|WP_004584358.1|1924588_1925002_+|PcfK-like-protein	1924588_1925002_+	137 aa aa	40	NA	NA	No	NA
NZ_CP024593.1|WP_099896811.1|2402508_2402925_-|PcfK-like-protein	2402508_2402925_-	138 aa aa	40	NA	NA	No	NA

Protein sequences of NZ_CP024593.1|WP_039417454.1|167175_167598_+|PcfK-like-protein

>NZ_CP024593.1|WP_039417454.1|167175_167598_+|PcfK-like-protein
MKGTEHFKNVIQNYLDERAQYDELFAENYRKKDKDMDSCIQYILNTVKQSGCNGFADDEIYSMAVHFFDEDNIDIGSPINAHVVAVVNQVVELTAEEKAQAHREAMQRAQEEAYRKMTQPTKKKAKTTVDTTLQPSLFDL

gnl|BL_ORD_ID|40 information

• hit_Aca_id: gnl|BL_ORD_ID|40
• identity: 0.5563380281690141
• query_coverage: 1.0
• hit_coverage: 0.9929078014184397

Protein sequences of NZ_CP024593.1|WP_004584358.1|1924588_1925002_+|PcfK-like-protein

>NZ_CP024593.1|WP_004584358.1|1924588_1925002_+|PcfK-like-protein
MKGTEHFKDVIQNYLETRASYDELFAGNFRKENKNIDECITYILTEVQRMGCAGLSDEEVYSLAVHYYDEDNIKVGTSINCQVVVNHTIELTEEEKAEARKKAIERYQAEEYRKLTAKKPKAEKQAEEQLQPSLFEF

gnl|BL_ORD_ID|40 information

• hit_Aca_id: gnl|BL_ORD_ID|40
• identity: 0.5815602836879432
• query_coverage: 1
• hit_coverage: 1.0

Protein sequences of NZ_CP024593.1|WP_099896811.1|2402508_2402925_-|PcfK-like-protein

>NZ_CP024593.1|WP_099896811.1|2402508_2402925_-|PcfK-like-protein
MKGTEHFKDVIQNYLETRASYDELFAESFRKENKSIDECITYILTEVQRMGCAGLSDEEVYSLAVHYYDEDNIEVGKSINCQVVVNHTIELTEEEKAEARKKAIERYQAEEYRKLTAKKPKAEKQVEQQIAQASLFEF

gnl|BL_ORD_ID|40 information

• hit_Aca_id: gnl|BL_ORD_ID|40
• identity: 0.5815602836879432
• query_coverage: 1
• hit_coverage: 1.0