CRISPRimmunity

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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_CP051167	Oxynema sp. AP17 chromosome, complete genome	28 crisprs	csa3,cas14j,cas14k,WYL,cas3,cas10d,csc2gr7,csc1gr5,cas6,cas4,cas1,cas2,Cas14c_CAS-V-F,c2c9_V-U4,Cas14u_CAS-V,DinG,cas10,cmr3gr5,cmr4gr7,cmr5gr11,csx1,csx18,csb2gr5,cas7,cas8u1,csm3gr7,csx19,csx10gr5,csx3,c2c10_CAS-V-U3	2	19	6	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP051167_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_1

754574-754797

TypeV

Consensus_repeat	Method
GGCGAAGAAGGAGACGACACCCTCAACGGCGGTGACGGCAACGA	PILER-CR

2 spacers

cas14j

The CRISPR arrays of NZ_CP051167_1

>merge|NZ_CP051167|1|754574-754797|PILER-CR
GGCGACGACACCCTCGACGGCGGCGACGGCGACGACCAGCTCAACGGCAACGAAGGAGCCGACCAACTCTTAGGTCAAGCCGGAAACGATACCTTAAATGGGGGAGAAGAAGCCGATACCCTCAACGGCGGTTCCGGGAACGACGTCGTACAAGGGGACGCGGATAATGACATTCTCTTCGGCGAAGAAGGAAACGACACCCTCAACGGCGGTGACGGCAACGA

>NZ_CP051167|1|1|754574-754797|PILER-CR
GGCGACGACACCCTCGACGGCGGCGACGGCGACGACCAGCTCAACG	GCAACGAAGGAGCCGACCAACTCTTAGGTCAAGCCGGAAACGATACCTTAAATGGGGGAGAAG
AAGCCGATACCCTCAACGGCGGTTCCGGGAACGACGTCGTACAAGG	GGACGCGGATAATGACATTCTCTTCGGCGAAGAAGGA
AACGACACCCTCAACGGCGGTGACGGCAACGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168567851.1\|760586_760946_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168567847.1\|756881_757454_+\|IS607-family-transposase	unknown	unknown	gnl\|CDD\|225296
NZ_CP051167.1\|WP_168567836.1\|738577_738823_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168567842.1\|747134_748187_-\|UPF0104-family-protein	unknown	unknown	gnl\|CDD\|377103
NZ_CP051167.1\|WP_168567835.1\|733600_738373_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|238923
NZ_CP051167.1\|WP_168567841.1\|746204_747083_+\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|293813
NZ_CP051167.1\|WP_168567846.1\|755627_756761_+\|transcription-termination/antitermination-protein-NusA	unknown	unknown	gnl\|CDD\|237063
NZ_CP051167.1\|WP_168567852.1\|762547_762697_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168567839.1\|741909_743790_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168567838.1\|739155_741765_+\|bifunctional-aconitate-hydratase-2/2-methylisocitrate-dehydratase	unknown	unknown	gnl\|CDD\|236424
NZ_CP051167.1\|WP_168567849.1\|758654_759359_+\|OmpA-family-protein	unknown	unknown	gnl\|CDD\|143586
NZ_CP051167.1\|WP_168567844.1\|750615_752769_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|335313
NZ_CP051167.1\|WP_168567840.1\|744194_745919_-\|potassium-channel-protein	unknown	unknown	gnl\|CDD\|367001
NZ_CP051167.1\|WP_168567855.1\|763850_766811_-\|response-regulator	unknown	unknown	gnl\|CDD\|236842
NZ_CP051167.1\|WP_168567848.1\|757401_758541_+\|transposase	cas14j	-	gnl\|CDD\|223747
NZ_CP051167.1\|WP_168567854.1\|763335_763716_-\|response-regulator	unknown	unknown	gnl\|CDD\|381164
NZ_CP051167.1\|WP_168567843.1\|748343_750515_+\|phosphodiesterase	unknown	unknown	gnl\|CDD\|226070
NZ_CP051167.1\|WP_168567837.1\|738914_739142_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168567850.1\|759522_760524_+\|methionyl-tRNA-formyltransferase	unknown	unknown	gnl\|CDD\|234567
NZ_CP051167.1\|WP_168567853.1\|762695_762941_+\|acetyltransferase	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168567847.1\|756881_757454_+\|IS607-family-transposase	gnl\|CDD\|225296	COG2452, COG2452, Predicted site-specific integrase-resolvase [DNA replication, recombination, and repair].	2.92435e-49
NZ_CP051167.1\|WP_168567842.1\|747134_748187_-\|UPF0104-family-protein	gnl\|CDD\|377103	pfam03706, LPG_synthase_TM, Lysylphosphatidylglycerol synthase TM region. LPG_synthase_TM is the N-terminal region of this family of bacterial phosphatidylglycerol lysyltransferases. The function of the family is to add lysyl groups to membrane lipids, and this region is the transmembrane domain of 7xTMs. In order to counteract attack by membrane-damaging external cationic antimicrobial molecules - from host immune systems, bacteriocins, defencins, etc - bacteria modify their anionic membrane phosphatidylglycerol with positively-charged L-lysine; this results in repulsion of the foreign cationic peptides.	0.00462334
NZ_CP051167.1\|WP_168567848.1\|757401_758541_+\|transposase	gnl\|CDD\|223747	COG0675, COG0675, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	1.78527e-21
NZ_CP051167.1\|WP_168567841.1\|746204_747083_+\|MBL-fold-metallo-hydrolase	gnl\|CDD\|293813	cd07727, YmaE-like_MBL-fold, uncharacterized subgroup which includes Bacillus subtilis YmaE and related proteins; MBL-fold metallo hydrolase domain. Includes the uncharacterized Bacillus subtilis YmaE and Nostoc all1228 proteins.Members of this subgroup belong to the MBL-fold metallo-hydrolase superfamily which is comprised mainly of hydrolytic enzymes which carry out a variety of biological functions. The class B metal beta-lactamases (MBLs) from which this fold was named are only a small fraction of the activities which are included in this superfamily. Activities carried out by superfamily members include class B beta-lactamases, hydroxyacylglutathione hydrolases, AHL (acyl homoserine lactone) lactonases, persulfide dioxygenases, flavodiiron proteins, cleavage and polyadenylation specificity factors such as the Int9 and Int11 subunits of Integrator, Sdsa1-like and AtsA-like arylsulfatases, 5'-exonucleases human SNM1A and yeast Pso2p, ribonuclease J and ribonuclease Z, cyclic nucleotide phosphodiesterases, insecticide hydrolases, and proteins required for natural transformation competence. Classical members of the superfamily are di-, or less commonly mono-, zinc-ion-dependent hydrolases, however the diversity of biological roles is reflected in variations in the active site metallo-chemistry. .	2.30591e-97
NZ_CP051167.1\|WP_168567846.1\|755627_756761_+\|transcription-termination/antitermination-protein-NusA	gnl\|CDD\|237063	PRK12329, nusA, transcription termination factor NusA.	1.38697e-132
NZ_CP051167.1\|WP_168567850.1\|759522_760524_+\|methionyl-tRNA-formyltransferase	gnl\|CDD\|234567	PRK00005, fmt, methionyl-tRNA formyltransferase; Reviewed.	5.75861e-152
NZ_CP051167.1\|WP_168567838.1\|739155_741765_+\|bifunctional-aconitate-hydratase-2/2-methylisocitrate-dehydratase	gnl\|CDD\|236424	PRK09238, PRK09238, bifunctional aconitate hydratase 2/2-methylisocitrate dehydratase; Validated.	0
NZ_CP051167.1\|WP_168567849.1\|758654_759359_+\|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.	2.3608e-41
NZ_CP051167.1\|WP_168567844.1\|750615_752769_+\|hypothetical-protein	gnl\|CDD\|335313	pfam03403, PAF-AH_p_II, Platelet-activating factor acetylhydrolase, isoform II. Platelet-activating factor acetylhydrolase (PAF-AH) is a subfamily of phospholipases A2, responsible for inactivation of platelet-activating factor through cleavage of an acetyl group. Three known PAF-AHs are the brain heterotrimeric PAF-AH Ib, whose catalytic beta and gamma subunits are aligned in pfam02266, the extracellular, plasma PAF-AH (pPAF-AH), and the intracellular PAF-AH isoform II (PAF-AH II). This family aligns pPAF-AH and PAF-AH II, whose similarity was previously noted.	5.103e-19
NZ_CP051167.1\|WP_168567840.1\|744194_745919_-\|potassium-channel-protein	gnl\|CDD\|367001	pfam02254, TrkA_N, TrkA-N domain. This domain is found in a wide variety of proteins. These protein include potassium channels, phosphoesterases, and various other transporters. This domain binds to NAD.	1.93741e-24
NZ_CP051167.1\|WP_168567854.1\|763335_763716_-\|response-regulator	gnl\|CDD\|381164	cd19937, REC_OmpR_BsPhoP-like, phosphoacceptor receiver (REC) domain of BsPhoP-like OmpR family response regulators. Bacillus subtilis PhoP (BsPhoP) is part of the PhoPR two-component system that participates in a signal transduction network that controls adaptation of the bacteria to phosphate deficiency by regulating (activating or repressing) genes of the Pho regulon upon phosphorylation by PhoR. When activated, PhoPR directs expression of phosphate scavenging enzymes, lowers synthesis of the phosphate-rich wall teichoic acid (WTA) and initiates synthesis of teichuronic acid, a non-phosphate containing replacement anionic polymer. Members of this subfamily belong to the OmpR family of DNA-binding response regulators, which are characterized by a REC domain and a winged helix-turn-helix (wHTH) DNA-binding output effector domain. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.23133e-35
NZ_CP051167.1\|WP_168567843.1\|748343_750515_+\|phosphodiesterase	gnl\|CDD\|226070	COG3540, PhoD, Phosphodiesterase/alkaline phosphatase D [Inorganic ion transport and metabolism].	5.64783e-41
NZ_CP051167.1\|WP_168567835.1\|733600_738373_-\|PAS-domain-S-box-protein	gnl\|CDD\|238923	cd01948, EAL, EAL domain. This domain is found in diverse bacterial signaling proteins. It is called EAL after its conserved residues and is also known as domain of unknown function 2 (DUF2). The EAL domain has been shown to stimulate degradation of a second messenger, cyclic di-GMP, and is a good candidate for a diguanylate phosphodiesterase function. Together with the GGDEF domain, EAL might be involved in regulating cell surface adhesiveness in bacteria.	1.14033e-103
NZ_CP051167.1\|WP_168567855.1\|763850_766811_-\|response-regulator	gnl\|CDD\|236842	PRK11091, PRK11091, aerobic respiration control sensor protein ArcB; Provisional.	3.743e-60

>NZ_CP051167.1|WP_168567844.1|750615_752769_+|hypothetical-protein
MLVAEDLFNEGYYLAKNPDIAAAIATGAISSAAEHFFTFGEVEGRDPSAFFDSRYYLETNPDVAAVVADFQFTALEHFIEFGQREGRSPTPFFDLTWYRDRHPDVAAAVDRDEITGSFVHYVLNGAEEGRSPSPIYDESFYLNANPDIAAAVGRDELTGIEHFISFGSAEGRRASEVFDSRFYLDTYPDVALAVSNGAIDSPAEHFLRSGRFEGRLSVPNVALPEPTGPLNVGQTSYQFRDPGRPEIFTPDPNDTREVGLKVWYPVGTNADNSSQPPFPPTLPPTQGNASYIRDAFISQAVATAQGVYPNFYNTIATNSRFNTAGLATTAERYPVILFAHGLGVIPDVYTNYFEDLASHGYIVGAIDHSYVAGISRLSNGAIAPFASNFLPADPSQLEGALTQTLAETSQDVSFILDQLAGVNANDPQRLFTGKLDLERVGIFGHSLGGLTAIAALQRDRRLDAAVSLDPTVISPQLVGAIDRPLMVMNAASTFDVDRSPIGQLLGFADRQLRPGLFQQATGSAYNVTIDGTEHEDFSDRPLLFPLQALYSPDRLGQAGGYDIGLTDIGRLDGDRLTAIVREYNTSFFDRHLKGESEPLLAGASLFPEVRFETRNSDVAVRESVRNAVLQQARSELALPDTNLGVFSITPTLWPDGCLGLSQPGEICTQAQVPGWSVLLSDPSQPPNQSFSYAYRTDFDGTEIRRDPSAIAPVSLPV
>NZ_CP051167.1|WP_168567843.1|748343_750515_+|phosphodiesterase
MLDLDTLFDERYYLATNPDVANAVNNGAIAPLQHFITFGQFERRDPSAIFDTDYYLSQYLDVADAVRQGSLAAVEHYLNFGQREGRDPGLLYDQSFYLSNNPDVAAAVAADQLTGIEHFLNFGEAEDRTPSRFYNPAYYLDRNPDVAAAVAADRLTGIQHYLEFGAIENRELSPFIEPGGSSLPNGVAAGDVTQTSAMLWARTTTPGPVNFEWNGGVAEIVATDPLVPVKLQLDGLQPNTEYTYTVSDSGGAIATGKFRTLAPPGRRTGLRFGVSGDWQGELAPYPSISNADSRNLDFFVQVGDTLEADSSSPDLPGVRQASSLLEFYTKHNEIYSERFGLNPWVDLRQSTATYSTWDDHDITNDFAGGAAPSESPQRNGIFGTGDGFVNETPVFREGLQAFQEFKPLQDQFYGETGDPRTANKQKLYRFNTHGSDAASFILDTRSFRDKPLPFLAETASEEEIAAYLQDAFEPGRTLLGRAQLEQLKTDLLTAENTGVTWKFVMSSVPMQHFGIPVAGERWEGYAAERTELLKFIEDNDIDNVVFVTGDFHGNVVNNVTYQEGFGQPQIQTGAMDVMVGPVGIQLNIGQGPFAAPFGPATVAFTPDALLPQSEKERYRGLTDVEEKNAFVRQVIDNRIVPLGYDPVGLEGSNIDARLLQGSYFAAHNYGWTEFEIDRDSQVLTVTTWGVEPYTESELEANPEAIASRTPTVRMQFEVTPETL
>NZ_CP051167.1|WP_168567842.1|747134_748187_-|UPF0104-family-protein
MSKSPLTWLKSVLSRGKPFIRWFVLGAIVFFLAQTVKDRAAEVASLQISRSGWLKLAIALCVTALAHIWSGWVWLWILRQFDPPPGSFRDRHVPLGRGLYIYLTTNVAKYLPGNVWHFYGRIKAIAESGTPFSVAALSVLLEPLLMAAAALAIAIFGSLNLATGDLSPTSPAFFDPLRFLKLLALFAVLVGVHPRLLNPVIQFLGKLKLKRQPPRSSSVSEATPEGLPVTDVPTEPIAAQLTRYPLSPFLGEIGFLLLRGSGFILTVDVMTSVQWSAIPTLMSGFSVAWLLGLVVPGAPGGIGIFEATAIAILSHQFSPAAILGAVAFYRLISILAESATAAIAWGLGKR
>NZ_CP051167.1|WP_168567841.1|746204_747083_+|MBL-fold-metallo-hydrolase
MATLKERRPENVDGEFYVDRTCIDCDTCRWMMPAVFHRDNGQSAVYRQPKNEGERLQALQALLSCPTASIGTVDRPKDIREAQESFPLAIADNVYHCGYHSEKSFGAASYLIRRQGGNILVDSPRFTPPLVKKLEAMGGIRYLYLTHRDDIADHQKFRDHFGCDRLLHEQEIREATQDIEIKLRGFDPIQFAPDLQIIPVPGHTEAHTVLLYDNRFLFTGDHLAWSDRLQSLIAFRNHCWYSWPKLVESMHDLAHYSFEWVLPGHGRRYHADRETMGKELQKLLDWMKTEAV
>NZ_CP051167.1|WP_168567840.1|744194_745919_-|potassium-channel-protein
MKPRIIVCGLGRTGYKIFSLLKQQGASVVGISTKPLDLPAESLRERESGSDIVVGELQSAETLMNAGIRQAHTLVIAGATDAVNLEILVQARILNPQIRIINRLFNASLGDRLDRTLPAHVSMSVSDLAAPVFSFAAFGNRAIGQLRLFNQTWPMHEECIDEHHPWKDRPLADLWDDRNRMLIYYLPAETSVDLVSAVIHGHTLKVGDRLIVATKPSIRTTRKSIVDRLKKFLTSVQRFYEHSQSSIWVTFVLFLTIFGTTVTYTWVTSETTFIDALYFSVGMITGAGGNEKVAEYSPDIIKVFTAAMMLVGAGVVGIYYALLNDLVLGTRFRQLWNSAPIPQKNHYIVCGLGGIGIKIASQLQASGYEVVAIDRDPNTRFLHTARALKIPVIQGDARLSSTLESARLCHADALLAVTSNDTANLEIALTAKGLAPKLPVVARNQDGHFSRMFQQVFEFDAVLSPTELAAPAFAAAALGGRIFGNGMTADTLWVALATLITPAHPFCTQRVKDAAMKADFVPLYIETNCSAIHGWDLLEICLSAGDVLYLTMPANKLELLWRTTPSLLLASSSS
>NZ_CP051167.1|WP_168567839.1|741909_743790_-|hypothetical-protein
MSPETQKFSLSALPTLLMSHPLLAASLGATETVPPNERAHEGRRLHAIPSLYDREATSPGYRPHSPGTNWERSGFDDRPPKIQALYQIALALSRSEGVERMEQLAADLPKASEREAFLCAIAVRSARAGEVEHTLATIARVQDPCLQIRSWREAIVVLTRGDRLADALEICDRLDPQERVAALCDMVVELRSLGHDDRALAMARTIPHVPQQGSLLQWLAYEWAKVRDFDRVGQALATIADPSQDKVAPMVHLAVVLAGEGQLDLARELAVAIERPDERSRVLAELAGAAIDRGETTRALSILHEAWQLCQPLPASAFKVVTIARISLEYAQAGATESSARILKEAIAAIETLKPKVSGRFPNRTGERLHATEYLNRDLPFNPFEDGAKTIARVRSLAREWVADAEGLAVPDGSEPTRPPRETRGEFSANSCTLIANRDLQAALEMAQGIGNTERRAKALRAIGVNLARADRVETGVQAIAAIADRHQQAAGLRQIALLLLDKGKVFKARLVADAIADFQLQAETLGAIALNLSGRGQILEARMVAQTIGDRREQARVLHQIALGLAEISQYNRSLQVSRSIDDRYAQARTLAAIAERLYALGQGDRAAKILDSALELAELDRFSP
>NZ_CP051167.1|WP_168567838.1|739155_741765_+|bifunctional-aconitate-hydratase-2/2-methylisocitrate-dehydratase
MLEAYRQHVEQRSALGIPPLPLDAQQTSELCELLKNPPSGEEDTLLYLLRERVPPGVDQAAYVKASFLTAVAKGEVNCPLISEIEAIEILGTMLGGYNVHALIELLQSDNGDKAQTAADALKKTLLVFDAMHDVLELAETNSYARQVVDSWAAAEWFTSRPTLPEAITVTVFKVPGETNTDDLSPASHATTRPDIPLHALSMLESRLEGALETIAELKQKGHPVAYVGDVVGTGSSRKSAINSVLWNLGQDIAHVPNKRGGGYILGGAIAPIFFNTAEDSGALPIECDVTALKTGMVVTLHPYKGEITDESGAVISRFSLKPNTIIDEVRAGGRIPLIIGRSLTDKVRKALGEPLSDIFTRPELPEENNKGFTLAQKMVGKACGLPGVRPGTACEPLMTTVGSQDTTGPMTRDELKELACLGFSADLVMQSFCHTAAYPKPVDVETHKELPDFFSTRGGVALRPGDGIIHSWMNRMLLPDTVGTGGDSHTRFPLGISFPAGSGLVAFAAALGVMPLDMPESVLVRFSGSLQPGVTLRDIVNAIPYVAIQQGLLTVAKENKKNIFSGRIMEMEGLPDLKVEQAFELTDATAERSCAGCTVKLGEATVAEYLRSNVALLKNMVARGYQDARTIMRRVAKMEQWLAKPELMDADKDAEYAAVLDVNLDEIKEPIVAAPNDPDNVKLMSECAGDRIDEVFIGSCMTNIGHYRAAAKVLENAGPVKVRLWICPPTRMDEEQLRKEGVYGTFAAAGARTEMPGCSLCMGNQARVEDNATVFSTSTRNFNNRMGKGARVYLGSAELAAVCALLGRIPTVEEYLDIVSEKIDPFAGDLYRYLNFDQIEGFEDEGRVVPLEEMPKIEDILGIPAVTQS
>NZ_CP051167.1|WP_168567837.1|738914_739142_+|hypothetical-protein
MGIGQIAAIATHKEPTPPDRRSHRHRRTRLTRYGSKCATNLYHPRETPQQRPSTPNVKVSTESTPLAKLRFAHAI
>NZ_CP051167.1|WP_168567836.1|738577_738823_+|hypothetical-protein
MFLTGVEHWQKTIASIAVQFLFKKNIFGFDRGHSLELQTGLENFENFDTFTRPHRPIRERGDRRDRPPASEIARPRPRFVK
>NZ_CP051167.1|WP_168567835.1|733600_738373_-|PAS-domain-S-box-protein
MGLVGHQRDRASTNRNLEKQSSKYTQKTTESSLQTRARPLPWLELPDPREKMFEGQSIYQQIGRDLPIAMALVRPSDGVIVYANPRLEKLFGYEDGQLVGCQTLQLYWNPNQRAELVQSVSERGEISDWPLLAKKIDGSPIWVSMNARQQPIADEALFLKTFIDITHFKQAKDTLKVLLDSPLGDGGTTCLGELARYLALAVGARSAFVAELVGGNDRPARIWVGNPQQPIQIQCSGCECLPQGEYWLNQTPWAQVLDLGQGSGWLPPEVVCFTDAFDSDGEPPCQYFGVRLEGRDGRALGLVGLIGDRHWSADEETDSILRCFAARATAELERRQLEEALQLERRKQQLTVEGGSILTYTLDLRGRPLQIEGSAPGILGGERVASAEENRAEIEAELAFDRYRQRPEISRAIARGLAGRAETWVESADGSLYRHETHPLYNTFGDPIGLFGKVRELPPTAAIYQGSRDPIAPQTESDLFVGGPVTVFQWQPRENWPVASVSPNVTQFGYHPQTFIEEGLCYAEIVHPDDLPRVAAEVEQFLAAGQDRFEQNYRICCANGESRWIRDFTVVVRDRHGEILHYRGYIVDITVSEATPKAFRQQALFALQESETRLRQALQAARMGVWDWERHSNRVTWSLGVEGMFGLPPGCFGDRPESYWQYVHPDDRATVRKAVMRAVSAKTNYYNEHRLLDPASGRVRWIAFQGDVVCDEAGAVLRMTGTVVDISDRKQTEAALTQSEAHFRAILNSSLQAVVFIDCDYRIQVFNKTARLATEAVWQKTIQPGDSIYEYVAPEDLEDFNRDFHAALAGHCISTQRNIRGNGTEDNWFEVSYYPVFDENDRVIGVCFIALDITERKAAVDALYRSEERFRSLVQYSSDTIAILTDRGAIAYTSPSSEKILGYTPEQLIGKNVFEYIHPDDRHSFQELFLTALARPDFLVEIECRFLHGNGEWIYLESVGSNRLDDPSIRGFVVNARDVTDRHQQEEWLKLLERAIAASNNGIVITDACAGDNPVVYVNRAFEEITGYRSAEVLGKNCRFLQGKNRDTTVLNRLRSAIRNGEDCTVILQNYRKDSTPFWNELRLSPVKNDRGRLTHFIGVQIDITERKNAEEKLIHQAYYDALTGLPNRALFMEQLHAASQRVKDRSDRLFAVLFIDLDRFKIVNDSLGHAIGDMLLVAIAYRLQKGLAELEGISSLAEAIDPPPPVAESLYNYRQSSSRRRSANFTVARLGGDHFTILLDNLHSLEEATVVAESIHAQLSAPFTFSGHEVFVTASIGIALSTTDYDAPADLLRNADLAMYAAKAAGKARYAVFDKAMHDRAVQRLQLENDLRRTLHDLETEGKTDLFLTYQPIVSLIDGHLVGFETLVRWQHPQKGLISPAQFIPLAEENGTIVPLGEWVLYEACQQLVRWQRDYPHACEHLSLSVNLSGKQFLQPDLVENIDRTLRETGLNPEALKLEITESVLMRDTEAATKTLLELKKRRIHLCLDDFGTGYSSLSHLAQFPIDTLKIDRSFVSRMISEGKDLEIVQAIVSLAHALDMNTIAEGIETAGQLVQLKSLGCQQGQGYWFSKPVDTDRATQLIRSSNRP
>NZ_CP051167.1|WP_168567846.1|755627_756761_+|transcription-termination/antitermination-protein-NusA
MSMVTLPGLSTLIESMSQQRNLPASAVQEALQEALLKGYERYRRQHGEDDPNLLSEDYFENFSVQLDLQAEGFRVVARKTIVEQVSQPDREISIASKGAQRARASLGQVVMVDVTPKQEAFGRLAAHQTKMVLTQKLQEQQCKFVQTHFAHLRGTVLDATVRRHDRRGVILAIDSGVDGLHVEAELPHYDKLPNDDYTEDAHFKVYLKKVYDNPSSRPLLRVSRASSHLIEGLLVETVPALREQQVEIKAISRDAIPRDREVTPRSKVAVASADPAIDPVAACLGDNGELVTAIGAQMNGEKIEILPWSEDPIALIATALSPAQVREVRLLDEEGREAVVVVAADQEALANGPNAQNLHLAARLTGWKLKLETVAAE
>NZ_CP051167.1|WP_168567847.1|756881_757454_+|IS607-family-transposase
MPKKYVTPKEAQAILGVSEKTLRNWDKQGKIRAIRIPSGHRRYDISSIDGKKNRARIIYARVSSHKQKADQDLQADYLLCLYPRAEVIKEIGSGLNYNRKKFKAILERVMSGDVEQLVVGHKDRLARFGFELLKWICELNHTELVVCNNTELSPEREMVEDILAIVHVFSYRLYGLRKYKSQIKEDPGLP
>NZ_CP051167.1|WP_168567848.1|757401_758541_+|transposase
MDSGNTSLKSKKIRVYPETELKMTWRKWLAASRYCYNAGMARLRDTYFEGLKLPSAYDLRQVVMSKIPEWVNSTPFNLRGAAVLDAHAAFKNTPKEHKLRPKFRSCRQPVSSFKLQSQNWRGGTTYPTHKTESGIKLKELKVNASEEIPAAIPSDFNVILDRGRWFIAYTVEEERLTNPHQQAIALDPGVRTFLTGFDGNKVIALGNGSISRIVKLCKRLDRIQSETAKAKGRDNKRKRFKLRKLARQLRIKIRNLVDECHKKTAAFLTSNYSQVMIPDFKSSFMVYRAKRKINHKTARSLLTWAHYRFKQRLVHQAVKRGCQVIEVTEEYTSKTCSKCGQIHNRLGGSKKFICPNCSHRIDRDANGSINVFLKTISGN
>NZ_CP051167.1|WP_168567849.1|758654_759359_+|OmpA-family-protein
MTHSAPDSPSNSKPLAILKGTAIAVWRLCLLGSLSAGFLLLGMAIAHFYPHPNPHRPLLDTAIRLGRGGTLPASQSPPRDVPSPASSPSPSVSPSESEDGDRLPTSAPADSANPAPAPEPLSVTLPSDVFFAPASSTLNPDKTELLDNIISDLRNYQGATIRIAGHTDNTGDARANQELSAQRARAVAQYLTETLGDRYQWQSVGYGETRPLADNDSDLNRQRNRRIEIEIQPK
>NZ_CP051167.1|WP_168567850.1|759522_760524_+|methionyl-tRNA-formyltransferase
MKVVFFGTPYFAVPSLEILLAHKHFEVAAVITQPDKRRRRGNQLIPSAIKKVALARGIPVWQPRSVKKDANTLAQLEKLAADVFVVVAYGQILSPEILAMPRLGCVNVHASLLPQYRGAAPIQWSLYDGVSETGLTTMLMDEGMDTGPMLLKAKTPVELLENADLLARNLSNMGGELLVETLLKLERDRIKPIPQDEERASYARLIQKSDYALDWSRRAIALHNQIRGFYPHCTAQFRGEPLKIMASAPVGDDYWEDLPPSFSVLEHNWPVLYSGGGAIGEVVCIAKHIGPIVQTGDGLLLLQQVQLAGKRAQSGWDFANGAHLQVGEILHNG
>NZ_CP051167.1|WP_168567851.1|760586_760946_-|hypothetical-protein
MEPDSLPTEVILTEPTRSLGKIQLDWNPQPGHYLDLEGKTYTVLERRHRYQLKSGRYRLQKIALYVQSARRPIETSTIDGRWVLGDATCRYNARSELIRCAVNPEGPCSECRFYEPQEA
>NZ_CP051167.1|WP_168567852.1|762547_762697_-|hypothetical-protein
MILTPGRFDIIARAMAVGYRAGAEGSGVGKMLRQMAIEIHPSYSTILSL
>NZ_CP051167.1|WP_168567853.1|762695_762941_+|acetyltransferase
MFLKEKSTGDLVEVMRIEDVYDPCLSEIMGRTHAGEEIQDPTTFTKAELIFPSGEALPRCWIDPEYAMLKARAQSFVIQVS
>NZ_CP051167.1|WP_168567854.1|763335_763716_-|response-regulator
MSKKILIVDDEPHIRILMEQTLEELEDEGVELLIEENGEAALKAIESERPQLVFLDVMMPKLNGFEVCNQVKNELKIEGVYIIMLTAKGQEFDKQKGCDVGADLYMTKPFDPDEVLERSIEVLGLE
>NZ_CP051167.1|WP_168567855.1|763850_766811_-|response-regulator
MSGPIEREERYFILPKRTKIPKPFFWGTIAICVLPFLLNRFGVDFGTYEAPFPFEEASQLHPHELANALHHTLAGSFVHTMLEWSAFCAAIFTVVLAFTHYNLTGEITTPIIGVALFCSGVMDAFHTLAADRLIEAVAGNENLIPFTWAICRLFNAAIAIVGVSIFLVKNPRLEREQQGSNVVFLLSISGLFGAIAYGAIYLCATSDSLPQTMFEGTLFARPWDVVPLVLFAIAGIWLYPRFHRRFPSVFSHALILSVVPNIATQAHMAFGSTELFDNDFNIGHFLKIVAYLVPLIGLILDYARTYQGIRQMNDALNIEIGERKQAETALQQAHDELELRVRQRTQELSESNSQLQSEIDRRVKMQAQVQRAKETSEEALAYLSTIIDNLADGLLVTDSLGQVTRFNSALVRLFGLEEPELIGKPCDEVLSPQVAELVAQTKGHPRQVFTAEIDLGNHRIGQALATAIAKRGDRAVSNGNTVREAIALDGDCLGTAILIRDVTAEKEVDRMKTDFISTVSHELRTPLTSVLGFAKIIKKKFDDTIVPVVPLDDRKVQRTVKQVGNNIEIILSEGQRLTALINDVLDIAKMEAGKIEWHFELSDMGQVVKRAIAATSSLLEAKDLQVVEVIDEELPEVFVDRDRLIQVMINLISNAVKFTSEGSITCHVTRIENHLSVSVADTGIGIAPEDLDKVFEKFKQVGETLTDKPQGTGLGLPICKQIIEHHGGRIWVESEVGRGSTFSFTLPISPTSAEQSQKLNLDLLLRQLKEHVVTTTPEIDRHTKTILVVDDDASIREYLRQELEAEQYCVREAKDGMEAIEQAKSLHPDLIVLDVMMPKMNGFDVAAVLKNDPQTMNIPIVILSIVQDKERGFRIGIDRYFTKPVETESLLEEIGTLLARGSSRKKILIVDEDVSTVKVLAEVLQTQGYTVSEASNGRECIEKALTVKPDTIIVDSIFVNQHNLMQLLRFEKGLENVLFILLDKKP

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Crispr_ID: NZ_CP051167_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_2

996676-996764

Orphan

Consensus_repeat	Method
GCGATCGCCCTCCCAGAAATGCGATCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051167_2

>merge|NZ_CP051167|2|996676-996764|CRISPRCasFinder
GCGATCGCCCTCCCAGAAATGCGATCGTTTTTTTGAGGGGCGATCGCCTTTTTTCCCAGAATGCGATCGCCCTCCCAGAAATGCGATCG

>NZ_CP051167|2|1|996676-996764|CRISPRCasFinder
GCGATCGCCCTCCCAGAAATGCGATCG	TTTTTTTGAGGGGCGATCGCCTTTTTTCCCAGAAT
GCGATCGCCCTCCCAGAAATGCGATCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168567988.1\|989974_993841_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238004
NZ_CP051167.1\|WP_168567998.1\|998830_1000435_-\|CHAT-domain-containing-protein	unknown	unknown	gnl\|CDD\|227328
NZ_CP051167.1\|WP_168568001.1\|1006374_1007001_-\|SMC-Scp-complex-subunit-ScpB	unknown	unknown	gnl\|CDD\|213521
NZ_CP051167.1\|WP_168568003.1\|1008124_1008376_-\|TIGR02450-family-Trp-rich-protein	unknown	unknown	gnl\|CDD\|370527
NZ_CP051167.1\|WP_168571729.1\|993944_994706_+\|peptidylprolyl-isomerase	unknown	unknown	gnl\|CDD\|275293
NZ_CP051167.1\|WP_168567992.1\|995872_996439_+\|Uma2-family-endonuclease	unknown	unknown	gnl\|CDD\|368559
NZ_CP051167.1\|WP_168567987.1\|985641_985944_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|376684
NZ_CP051167.1\|WP_168567997.1\|998384_998627_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568000.1\|1005035_1005980_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168567989.1\|994780_995002_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168567996.1\|997636_997906_+\|type-II-toxin-antitoxin-system-ParD-family-antitoxin	unknown	unknown	gnl\|CDD\|274227
NZ_CP051167.1\|WP_168567986.1\|983538_985317_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571696.1\|988844_989864_-\|IS4-family-transposase	unknown	unknown	gnl\|CDD\|376573
NZ_CP051167.1\|WP_168567991.1\|995511_995847_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168567990.1\|995057_995456_-\|endonuclease-domain-containing-protein	unknown	unknown	gnl\|CDD\|238509
NZ_CP051167.1\|WP_168567995.1\|997145_997457_-\|DUF433-domain-containing-protein	unknown	unknown	gnl\|CDD\|225291
NZ_CP051167.1\|WP_168568002.1\|1007209_1008061_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP051167.1\|WP_168567985.1\|982028_983528_-\|DUF1822-family-protein	unknown	unknown	gnl\|CDD\|370155
NZ_CP051167.1\|WP_168567999.1\|1002708_1004658_-\|CHAT-domain-containing-protein	unknown	unknown	gnl\|CDD\|227328
NZ_CP051167.1\|WP_168567994.1\|996817_997153_-\|DUF5615-family-PIN-like-protein	unknown	unknown	gnl\|CDD\|375906

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168567988.1\|989974_993841_+\|hypothetical-protein	gnl\|CDD\|238004	cd00044, CysPc, Calpains, domains IIa, IIb; calcium-dependent cytoplasmic cysteine proteinases, papain-like. Functions in cytoskeletal remodeling processes, cell differentiation, apoptosis and signal transduction.	5.51695e-36
NZ_CP051167.1\|WP_168567998.1\|998830_1000435_-\|CHAT-domain-containing-protein	gnl\|CDD\|227328	COG4995, COG4995, Uncharacterized protein conserved in bacteria [Function unknown].	4.25762e-93
NZ_CP051167.1\|WP_168568003.1\|1008124_1008376_-\|TIGR02450-family-Trp-rich-protein	gnl\|CDD\|370527	pfam09493, DUF2389, Tryptophan-rich protein (DUF2389). Members of this family are small hypothetical proteins of 60 to 100 residues from Cyanobacteria and some Proteobacteria. Prochlorococcus marinus strains have two members, other species one only. Interestingly, of the eight most conserved residues, four are aromatic and three are invariant tryptophans. It appears all species that encode this protein can synthesize tryptophan de novo.	6.1185e-25
NZ_CP051167.1\|WP_168571729.1\|993944_994706_+\|peptidylprolyl-isomerase	gnl\|CDD\|275293	TIGR04500, PpiC_rel_mature, putative peptide maturation system protein. Members of this protein family have a novel N-terminal sequence region. Close homologs to the C-terminal region of this protein score well to PpiC-type peptidyl-prolyl cis-trans isomerase models (see pfam00639), yet no sequence within the family scores well to such models, suggesting origin within a branch of the PpiC family but subsequent neofunctionalization with a rapid change of sequence. The genome context for members always includes an ATP-grasp enzyme associated with peptide modification and a short polypeptide likely to be the modification target.	1.94256e-15
NZ_CP051167.1\|WP_168567992.1\|995872_996439_+\|Uma2-family-endonuclease	gnl\|CDD\|368559	pfam05685, Uma2, Putative restriction endonuclease. This family consists of hypothetical proteins that are greatly expanded in cyanobacteria. The proteins are found sporadically in other bacteria. A small number of member proteins also contain pfam02861 domains that are involved in protein interactions. Solutions of several structures for members of this family show that it is likely to be acting as an endonuclease.	1.86072e-31
NZ_CP051167.1\|WP_168567987.1\|985641_985944_+\|hypothetical-protein	gnl\|CDD\|376684	pfam01957, NfeD, NfeD-like C-terminal, partner-binding. NfeD-like proteins are widely distributed throughout prokaryotes and are frequently associated with genes encoding stomatin-like proteins (slipins). There appear to be three major groups: an ancestral group with only an N-terminal serine protease domain and this C-terminal beta sheet-rich domain which is structurally very similar to the OB-fold domain, associated with its neighboring slipin cluster; a second major group with an additional middle, membrane-spanning domain, associated in some species with eoslipin and in others with yqfA; a final 'artificial' group which unites truncated forms lacking the protease region and associated with their ancestral gene partner, either yqfA or eoslipin. This NefD, C-terminal, domain appears to be the major one for relating to the associated protein. NfeD homologs are clearly reliant on their conserved gene neighbor which is assumed to be necessary for function, either through direct physical interaction or by functioning in the same pathway, possibly involve with lipid-rafts.	2.46667e-10
NZ_CP051167.1\|WP_168568001.1\|1006374_1007001_-\|SMC-Scp-complex-subunit-ScpB	gnl\|CDD\|213521	TIGR00281, Segregation_and_condensation_protein_B, segregation and condensation protein B. Shown to be required for chromosome segregation and condensation in B. subtilis. [Cellular processes, Cell division, DNA metabolism, Chromosome-associated proteins].	3.15791e-41
NZ_CP051167.1\|WP_168567996.1\|997636_997906_+\|type-II-toxin-antitoxin-system-ParD-family-antitoxin	gnl\|CDD\|274227	TIGR02606, Antitoxin_ParD, putative addiction module antidote protein, CC2985 family. This bacterial protein family has a very similar seed alignment to that of pfam03693 but is a more stringent model with higher cutoff scores. Proteins that score above the trusted cutoff to this model almost invariably are found adjacent to a ParE family protein (pfam05016), where ParE is the killing partner of an addiction module for plasmid stabilization. Members of this family, therefore, are putative addiction module antidote proteins. Some are encoded on plasmids or in prophage regions, but others appear chromosomal. A genome may contain several identical copies, such as the four in Magnetococcus sp. MC-1. This family is named for one member, CC2985 of Caulobacter crescentus CB15. [Cellular processes, Other, Mobile and extrachromosomal element functions, Plasmid functions].	1.30837e-05
NZ_CP051167.1\|WP_168571696.1\|988844_989864_-\|IS4-family-transposase	gnl\|CDD\|376573	pfam01609, DDE_Tnp_1, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction. This family contains transposases for IS4, IS421, IS5377, IS427, IS402, IS1355, IS5, which was original isolated in bacteriophage lambda.	2.86696e-21
NZ_CP051167.1\|WP_168567990.1\|995057_995456_-\|endonuclease-domain-containing-protein	gnl\|CDD\|238509	cd01038, Endonuclease_DUF559, Domain of unknown function, appears to be related to a diverse group of endonucleases.	1.44978e-38
NZ_CP051167.1\|WP_168567995.1\|997145_997457_-\|DUF433-domain-containing-protein	gnl\|CDD\|225291	COG2442, COG2442, Uncharacterized conserved protein [Function unknown].	1.96479e-23
NZ_CP051167.1\|WP_168568002.1\|1007209_1008061_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	2.05317e-115
NZ_CP051167.1\|WP_168567985.1\|982028_983528_-\|DUF1822-family-protein	gnl\|CDD\|370155	pfam08852, DUF1822, Protein of unknown function (DUF1822). This family of proteins are functionally uncharacterized.	4.27764e-34
NZ_CP051167.1\|WP_168567999.1\|1002708_1004658_-\|CHAT-domain-containing-protein	gnl\|CDD\|227328	COG4995, COG4995, Uncharacterized protein conserved in bacteria [Function unknown].	5.66519e-83
NZ_CP051167.1\|WP_168567994.1\|996817_997153_-\|DUF5615-family-PIN-like-protein	gnl\|CDD\|375906	pfam18480, DUF5615, Domain of unknown function (DUF5615). This is a domain of unknown function found in potential toxin-antitoxin system component.	1.52682e-18

>NZ_CP051167.1|WP_168567992.1|995872_996439_+|Uma2-family-endonuclease
MPEMTIKDVERIESILSDAGLDCQLELEEGRIIIKNPSDLIASEVSVEFASQLSNWVKPRRLGRVFDSAGGFILPNSDLKAPDVSFVLRSRLPRSVRYFATLVPDLVVEVKSQSDRIKKLREKIKVYLEQGVQVAILIDPDTCLVEVYRPDTSVQTLGNGDILTVPELLPEWELVVEELWPVIFEDEE
>NZ_CP051167.1|WP_168567991.1|995511_995847_-|hypothetical-protein
MIYCNKKRAIAVLEKGDRSLGKKRSLSGIKRRSLSGKKAIALWEKEAIAFWDKKAIALWEKGDRISGRAIALNRDVNKLAPLSKGGWGDPTPDRLLVVSPEIPSERRVNLH
>NZ_CP051167.1|WP_168567990.1|995057_995456_-|endonuclease-domain-containing-protein
MTKFTNSQFHLPYNPKLVSIAKQMRQNPTPAEKKLWQDCLRKFPLRILRQRPIDNFIVDFYCASLKLVIGIDGESHFTQQGQDYDEERTRILEGYGITVVRFTNVDVLQNFEGVCRQLERWIPPTPLGKGGF
>NZ_CP051167.1|WP_168567989.1|994780_995002_+|hypothetical-protein
MLPASSLVALPTLQAFNRCDRLFFPECDRLFFPECDRLFIPESDRFFPRERSPFYPRERSPFSSESDRSFSRM
>NZ_CP051167.1|WP_168571729.1|993944_994706_+|peptidylprolyl-isomerase
MDSIPFLTINNQTISLSQAIGYLKASGKFGLFLSEILRQYILTHELDELESIDIALEELEQTILNFRLNNQLLDQNKFQDWLVKNGISYVNFRQRITNDLKLDKLKAKISEPKIEEYFKTQKQFFDRVVLSRIILNDKALAQKLNEELLADPRKFETLAREYSITDDRVVNGMMGPVSRGTLPDILKNPIEFSPVGEIIGPLEIDENYGLFRVEQFLDASLDDPKLKQELQNQLFEQWLQEKLQSLEIKLEVK
>NZ_CP051167.1|WP_168567988.1|989974_993841_+|hypothetical-protein
MRFVGGSVAGTDKISIGAYDGQDWGLQFAIITTQKVNQAPVVTAYNQTVNSGSSTSLSFSVTDPDGDQIRYYYFSDNNSSSTSGYFTVNGVKQTSGFYVDPDKLNTVRFVGGSAAGTDPIRIWAYDGQDWGYKDATMTTQQVNRAPVVTAYDRTVNSGSSNSLSFSASDPDGDRISYYYFSDYNTSSTSGYFTLNGVKQTSSFSVAADNLNTVRFVGGSAAGTDEIRIWAYDGQTWGSNDATITTQQANRAPVVTAYDRTVNSGSSNSLSFSASDPDGDRISYYYFSDYNTSSTSGYFTLNGVKQTSSFSVAADNLNTVRFVGGSAAGTDEIRIWAYDGQTWGSNDATITTQQANRAPVVTAYDRTVNSGSSINPGFYVSDPDGDQITRYYFSDYNTSSTSGYFTLNGVKQTSSFFVDADKLNTVRFVGGSATGTDQIRIWAYDGQTWGSNDATITTQKVNRAPVVTAYNQTVRRNQSIQPSFSVTDADGDTMTRYAFFDGNTSSTSGYFTVNGVKQAAGQTFYVNADQLNTVRFVGGSSNSNDYVYTRAYDGSAWSNWKDYLMKTEGGSKPVVSATDQTVKRNQSIQPSFSVTDADGDTMTRYRFFDGDNSSTSGYFTVNGVKKAAHQTFYVDADQLHTVRFVGGSVAGNDRVYVSATDGLDGWSTWQDYLMKTEGGSKPVVSATDQTVKRNQSIQPSFSVTDADGDTMTRYRFFDGDNSSTSGYFTVNGVKKAAHQTFYVDADQLHTVRFVGGSVAGNDRVYVSATDGIDGWSTWQDYLMKTQSGSNPVVTASDQTVNANESMKLSFSVTDADGDTMTRYAFFDGNSSSTSGYFTVNGVKQAAGQTFYVDADKLDTVRFVGGAVAGIDGLHVRTSDGVDGWSEWTKFNVSTKATVINDWFEQNIKDAAIRSLARSRFQDGELDRKDMIDIFINATDSGVVDAYEFADLQTLTSNKDYIKMPDYVQILSTKISHGNPANKSYRGTYLGNLQAGSSGEHLGKLIKKHFLGQDHPLPKGEYSYGSASNVEYRYAEGQLFQNGISYEDIKQGAVGDCYYLASLAAVAQKTPNVIKDMFIDNGIDEDGNRTYTVRFYNNGQVDYVTVDRYLPTNKNNGSLPFAGVGNGHTYKNSNNELWVALAEKAYAQMNEAGWMKRYTTDEGIDLHGLNSYKGIEGGWTNVSVAHINNQSGTRHSISSSTASSVVTAFNFGKLVNFSSLGKEATHGSPVVSSHAYTMVDYNQSTGKFKLFNPWGLDGGTEPGDSAFKPGILEMSWNEIKTYFRYWRVNG
>NZ_CP051167.1|WP_168571696.1|988844_989864_-|IS4-family-transposase
MVSNFPEILQKHLSHLPQDDYPVLDTFKFVSIWLNFILDQSQTTMRSLFKRLNIRGESVDISTFSKASKTRSPEVFHRLWDELKKEVAKKSQNSDKELMIFPLDSTIITLTSKLLWHQGYHQLKLFSGINLVTGNPGGISIHLGQGHDSKYGNETIEATPENGVAVMDRGFCSLERIAQLQAQKNRYFVLRIRKNIKLEMLENGEYLMGTGTAQVQGRVVMFCDREEKTEFRLVTNLPETGEGGISNEEIGEFYRLRWQIELLWKFLKMHLKLDKFITKNVNGMEIQIYCCLIGYLILKLVKINQEWGSSLLDKLRYLQAFMCEKISYVHWFRELVFHH
>NZ_CP051167.1|WP_168567987.1|985641_985944_+|hypothetical-protein
MSATFWQWLTRSLFQHPVSNPSSELNPSDFDSIAIVDEPIYPYQLGRVQFRCSWWPARCLQETVISPGQLVRVVGQHNITLLVEPTRFSVRDKTPQSQPE
>NZ_CP051167.1|WP_168567986.1|983538_985317_-|hypothetical-protein
MVYFPEPRHFAERFTSVLAFTSEGGRLIPRLQSQPRLRRNFELYRANHPEFALLCDRPSHEAETELALFWRDLAINGSPDDREAWESFRREQLAIAHLISFFERTCCQVVNQSASHCPELPIEDSLSILRGTVGNEQQLKEWLEKYDPQRGALLETYIHQILRNTLKAELNFGRVSKWRRFYKTSEEDLKYALEMNGYREPQITQFLWGRKIFKKVYLINHIQSPTRISGSKWLEPKLEDFQEAANCFNAERILPSVPLEISSYSIDLSALQLKRWMENCWESLRQTNSNTLISTAEIPDLETPDSPDSLDTLETPPSLFSGFSDSQLEQELNQCKNILKIQIGKSSIPVDPDKVLFLYYGINLTQSDIGKCLEIQQYKISRLVARYKRRLAKCLKQSSNPDGWILQYVRRWLRSKYPTADRSDLIEKALIEAVEALDSEDRRFLGDLLRRDPSFSSGFQEESLNSEELATLEKIENQLKQQLLYELEGWIDRYINSWLECFYRNALNTLLQEVTNSDLLETLTIENGSGLSHQDGKAKNYNTSISLEVLELYLQNWLTQNLGVYIENLKSWEKISRILSQWLEQQDWNQYS
>NZ_CP051167.1|WP_168567985.1|982028_983528_-|DUF1822-family-protein
MLKDRRTHTGRETHTFSISIPKMIRETGWQLAQNQSNPLSRYTAYLNRICLDTLLPFFHEWTEEEGLEKPLKWPREEQLFQSLEFVSGTALQIGEIRIVLIPYEIEECREFVVPQEWVDCPAYCGDYYLAVAVNLDLEEQENWLKIEGFTTHQQLKTVAHHRESDRTYTMEFNALVRDLNLIDLTDNLKVREPLPDLPQIEPGEVEQLLNMLGDAALYSPRLRTDISTDKWLSLINHCSYQKKLYARKMGEDLTEKNNSTEPITLKKWLGAIAEETQKILKEGWQSFDSLFEPLEPSPVRGHLSIDRHLTEPIDSKSEAAISPIISLLEPYQKKNLRYHAAGVLGEIGRGHPEAIAALSDLLKIEKDEEMRWQAALSLGKIDPGNPISGTKKAKLIDLGLRLHAREIALIIAIIPKDEERLGVFVQVRSVNEELPTGLKLSILSETGEVIPKLEVEARSDTAGEGKDNSIQLRFTPPSGTIFQVRVTSNDREFTETFIA
>NZ_CP051167.1|WP_168567994.1|996817_997153_-|DUF5615-family-PIN-like-protein
MPKTIRFHLDENVSNAIAEGLRRRGIDVTTTPESGLIGVSDEEQIALCREQERVIFTQDTDFLRMAQIGISHRGIIYCQQKTRSIGDIVRGITLIWEYLESEEIQDKVEFI
>NZ_CP051167.1|WP_168567995.1|997145_997457_-|DUF433-domain-containing-protein
MEMVITEHIEITPGVCGGKPRIAGHRIKVQDIVIWYEEMGMSPDEILYHHPSISLADVYAALAYYHDHREEIRRQLREDEAFAREMQAQTPSLLQEKLKHRNA
>NZ_CP051167.1|WP_168567996.1|997636_997906_+|type-II-toxin-antitoxin-system-ParD-family-antitoxin
MKSINISLPDSMRAYVEEVVAKEGYSTLSEYFRELVRQDQKRKATERLETLLLEGLESGTATAIAPQDWQDIRSAVRERLAKRSQPTED
>NZ_CP051167.1|WP_168567997.1|998384_998627_-|hypothetical-protein
MENDRTLGKRGDRISGRAIALREKRRSPLKKTIAFLGGRSLSEKKQGIERQCRGDSRIAPTTNPAFWKTIALWEKEAIAL
>NZ_CP051167.1|WP_168567998.1|998830_1000435_-|CHAT-domain-containing-protein
MKIHRILWVIIVTGTGLAIATCPGLTQTGNQSDITGPNMSDITGPDLEDFGFDEEFYEEFDEEFDEEFDEEFDEEFDYFDDEIDRGEYESQLEQLEIDISLEFIEEYQAIEFSDYLGVDLFGEIPSLEEIAKTLYDLWQTTGQKSAFIYVTSRDRSLDIVTVFPDESLSQSLVSSRVKHPEILTNIFTQDRQKQFTQKAIVPDVDRQKLLADVTKFRLQILSPQYRNSQQYLPLSKKLYQLLIAPIEDRLKAENIQNLVFSMDSGLRYLPLAVLHDGEQFLIEKYGVSLVPSFGLTDITYVDIRDRPVLAMGSAKFEGLPALPGVPLEVTNILEIPWMGESFINEQFTLDNFKQQAASQNFGVIHLATHAEFKPGRLENSYIQFFEDKLNLVQFRQLAQELGWTSVENPPIELLVLSACRTALGEEQAELGFAGLAVLSGVKSVLGSLWYVSDAATLGLMSEFYHHLRKTPIKVQALRESQLALLQGKVEVKNGLLYLSTGETLALPPELAQFEGMNFSHPYYWSAFTLIGNWN
>NZ_CP051167.1|WP_168567999.1|1002708_1004658_-|CHAT-domain-containing-protein
MYSLRWFLTPAITSFGVILLSQFPTIAQNQSDVTGPNVDPPLNQSDITGPQPIEISPIDLIEPLETEEPNNIIDETPPVDDAIVDNPNQQQPQNNSTPNNPIDTVPVDNDSDSPGLPVSDGNVVPENPTDFSENPQNNSGEPSIADSTTTTENSSENIDNIDRNNSVHVETSRPIEASILDAFFGDENTELEVDRQRYENLVAQSDIPTTLQLFEEFYALEFSNFLGIELFGKVAQVDEIAAKLYEMWQVTGKKAAFLYISSYEDRLELLLIPPVPPLDGSEITPVSRLKTIPKQQPTIAQGYLEEVISHSERHVIPNLSSEIVSKEIGLFQNAITDPRKRGSSQYLPHAQQLYQWFVDPVNVSLQEKEIDILVLAVNQGLRSVPFSALHDGDRFLIEKYALTLVPSFGLTDISFVDFRNSPILAMGASEFSELNDLPAVPLELEEIANSGLPTDAFLNEGFTVENFLQQNENKQYRGIHIATHAEFRPGALSNSYIYFYNNKIGLDRLRKITDRLGWNLTTTPAIELLTLSACRTALGDPQAELGFAGLAVLYGAKSALASLWYVSDEGTLGLMGEFYNHLQNNPLKSIALQEAQLAMLRGETYSENGLLHFSNGQTTAWEDETKSQQKFDYSHPYYWSAFSLIGNWN
>NZ_CP051167.1|WP_168568000.1|1005035_1005980_-|hypothetical-protein
MKLILTPIAIAVMFCPRAIAIPLDLEREREHFDPEPISIQPLRIGQATPPPDSTPSSSPGSLHRKQGNEQRFQPQRVPFRPRPNQGKPSAAASPGITIMNPSGYGASWGTLGIGLGLQERTRFTEDADGVMGIGMGFGDPRKNVGVALGVTVTDLWGDAFEDGTLSIKLHRRLPADFSVAAGVQGAVRWGETDGGSSVYGVVSRRFALQEDPSKPLSQLFLSVGVGGGQYRTEDQIDDGVDTVGLFGSAALRLYEPVNAVVEWTGQDLTVGLSIAPFRNVPIVISPALTDITGSAGDGTRFILGIGYGFSFDRF
>NZ_CP051167.1|WP_168568001.1|1006374_1007001_-|SMC-Scp-complex-subunit-ScpB
MTRLATTIEAILYLKGKPLSLAEIAEFAQCDKEDAEEALIELMGDYAHRESALEIVESNKGYTLQLRETFQDLVHSLIPAELGVGALRTLAAIALKKGSMSQTELVELRGSGAYQHVQELIQQGFVRRRRQSDGRSYWLQVTDKFHQYFQTEQLPQQLQLPLTSDRDEEAENGLENPSETAPETAPETAPETQATAANPAPVGPLPEG
>NZ_CP051167.1|WP_168568002.1|1007209_1008061_-|ABC-transporter-ATP-binding-protein
MSAAVCVENVRKIYDRTPVVNGLSFAIAPGEMFGLLGPNGAGKSTTIRMLTTLTRPSEGTIQVAGYDVRRDPIAVKQQIGVVLQQTSVDLDLTVWENMEFHGRLHHIPKTERQQRIDRALTYVELSDRQDVKAKTLSGGMKRRLQIARALLHEPKILFLDEPTVGLDPQTRRRLWEIIRDLNRQGMTMLLTTHYMEEVEYLCDRIGIMDAGTLIELGTLDELRHKHGGGLVMKQVGDRWEYKFFPDLDAANAYFEAQPDKTGLMVRPSNLEDIFVELTGRQLD
>NZ_CP051167.1|WP_168568003.1|1008124_1008376_-|TIGR02450-family-Trp-rich-protein
MAKKKQKFPYLVGSKWTARQKTWGWRHFQVVNRKNDGKWVFAEMVASCDPNVRFWLNARQLKDENLWQAGWQTLTEMGQEREG

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Crispr_ID: NZ_CP051167_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_3

998504-998595

Orphan

Consensus_repeat	Method
AGAGCGATCGCCCTCCCAGAAATGCGATCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051167_3

>merge|NZ_CP051167|3|998504-998595|CRISPRCasFinder
AGAGCGATCGCCCTCCCAGAAATGCGATCGTTTTTTTGAGGGGCGATCGCCTTTTTTCCCTCAGAGCGATCGCCCTCCCAGAAATGCGATCG

>NZ_CP051167|3|2|998504-998595|CRISPRCasFinder
AGAGCGATCGCCCTCCCAGAAATGCGATCG	TTTTTTTGAGGGGCGATCGCCTTTTTTCCCTC
AGAGCGATCGCCCTCCCAGAAATGCGATCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168567988.1\|989974_993841_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238004
NZ_CP051167.1\|WP_168567999.1\|1002708_1004658_-\|CHAT-domain-containing-protein	unknown	unknown	gnl\|CDD\|227328
NZ_CP051167.1\|WP_168568003.1\|1008124_1008376_-\|TIGR02450-family-Trp-rich-protein	unknown	unknown	gnl\|CDD\|370527
NZ_CP051167.1\|WP_168568004.1\|1008486_1010478_-\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|274362
NZ_CP051167.1\|WP_168568007.1\|1012499_1014275_+\|PEP-CTERM-sorting-domain-containing-protein	unknown	unknown	gnl\|CDD\|131644
NZ_CP051167.1\|WP_168567992.1\|995872_996439_+\|Uma2-family-endonuclease	unknown	unknown	gnl\|CDD\|368559
NZ_CP051167.1\|WP_168567998.1\|998830_1000435_-\|CHAT-domain-containing-protein	unknown	unknown	gnl\|CDD\|227328
NZ_CP051167.1\|WP_168568006.1\|1012329_1012503_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568000.1\|1005035_1005980_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168567989.1\|994780_995002_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168567996.1\|997636_997906_+\|type-II-toxin-antitoxin-system-ParD-family-antitoxin	unknown	unknown	gnl\|CDD\|274227
NZ_CP051167.1\|WP_168567993.1\|996453_996831_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568005.1\|1010483_1011416_-\|phosphate/phosphite/phosphonate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|379006
NZ_CP051167.1\|WP_168568001.1\|1006374_1007001_-\|SMC-Scp-complex-subunit-ScpB	unknown	unknown	gnl\|CDD\|213521
NZ_CP051167.1\|WP_168567991.1\|995511_995847_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168567990.1\|995057_995456_-\|endonuclease-domain-containing-protein	unknown	unknown	gnl\|CDD\|238509
NZ_CP051167.1\|WP_168567995.1\|997145_997457_-\|DUF433-domain-containing-protein	unknown	unknown	gnl\|CDD\|225291
NZ_CP051167.1\|WP_168568002.1\|1007209_1008061_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP051167.1\|WP_168567994.1\|996817_997153_-\|DUF5615-family-PIN-like-protein	unknown	unknown	gnl\|CDD\|375906
NZ_CP051167.1\|WP_168571729.1\|993944_994706_+\|peptidylprolyl-isomerase	unknown	unknown	gnl\|CDD\|275293

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168567988.1\|989974_993841_+\|hypothetical-protein	gnl\|CDD\|238004	cd00044, CysPc, Calpains, domains IIa, IIb; calcium-dependent cytoplasmic cysteine proteinases, papain-like. Functions in cytoskeletal remodeling processes, cell differentiation, apoptosis and signal transduction.	5.51695e-36
NZ_CP051167.1\|WP_168567999.1\|1002708_1004658_-\|CHAT-domain-containing-protein	gnl\|CDD\|227328	COG4995, COG4995, Uncharacterized protein conserved in bacteria [Function unknown].	5.66519e-83
NZ_CP051167.1\|WP_168568003.1\|1008124_1008376_-\|TIGR02450-family-Trp-rich-protein	gnl\|CDD\|370527	pfam09493, DUF2389, Tryptophan-rich protein (DUF2389). Members of this family are small hypothetical proteins of 60 to 100 residues from Cyanobacteria and some Proteobacteria. Prochlorococcus marinus strains have two members, other species one only. Interestingly, of the eight most conserved residues, four are aromatic and three are invariant tryptophans. It appears all species that encode this protein can synthesize tryptophan de novo.	6.1185e-25
NZ_CP051167.1\|WP_168568004.1\|1008486_1010478_-\|HAMP-domain-containing-protein	gnl\|CDD\|274362	TIGR02956, sensor_protein_TorS, TMAO reductase sytem sensor TorS. This protein, TorS, is part of a regulatory system for the torCAD operon that encodes the pterin molybdenum cofactor-containing enzyme trimethylamine-N-oxide (TMAO) reductase (TorA), a cognate chaperone (TorD), and a penta-haem cytochrome (TorC). TorS works together with the inducer-binding protein TorT and the response regulator TorR. TorS contains histidine kinase ATPase (pfam02518), HAMP (pfam00672), phosphoacceptor (pfam00512), and phosphotransfer (pfam01627) domains and a response regulator receiver domain (pfam00072). [Signal transduction, Two-component systems].	8.66907e-54
NZ_CP051167.1\|WP_168567994.1\|996817_997153_-\|DUF5615-family-PIN-like-protein	gnl\|CDD\|375906	pfam18480, DUF5615, Domain of unknown function (DUF5615). This is a domain of unknown function found in potential toxin-antitoxin system component.	1.52682e-18
NZ_CP051167.1\|WP_168568007.1\|1012499_1014275_+\|PEP-CTERM-sorting-domain-containing-protein	gnl\|CDD\|131644	TIGR02595, conserved_hypothetical_protein, PEP-CTERM protein-sorting domain. This model describes a 25-residue domain that includes a near-invariant Pro-Glu-Pro (PEP) motif, a thirteen residue strongly hydrophobic sequence likely to span the membrane, and a five-residue strongly basic motif that often contains four Arg residues. In nearly every case, this motif is found within nine residues, and usually within five residues, of the extreme C-terminus of the protein. Proteins with this motif typically have signal sequences at the N-terminus. This region appears many times per genome or not at all, and co-occurs in genomes with a proposed protein-sorting integral membrane protein we designate exosortase (see TIGR02602). PEP-CTERM proteins frequently are poorly conserved, Ser/Thr-rich proteins and may become extensively modified proteinaceous constituents of extracellular material in bacterial biofilms. [Cell envelope, Surface structures].	0.00271611
NZ_CP051167.1\|WP_168567992.1\|995872_996439_+\|Uma2-family-endonuclease	gnl\|CDD\|368559	pfam05685, Uma2, Putative restriction endonuclease. This family consists of hypothetical proteins that are greatly expanded in cyanobacteria. The proteins are found sporadically in other bacteria. A small number of member proteins also contain pfam02861 domains that are involved in protein interactions. Solutions of several structures for members of this family show that it is likely to be acting as an endonuclease.	1.86072e-31
NZ_CP051167.1\|WP_168567998.1\|998830_1000435_-\|CHAT-domain-containing-protein	gnl\|CDD\|227328	COG4995, COG4995, Uncharacterized protein conserved in bacteria [Function unknown].	4.25762e-93
NZ_CP051167.1\|WP_168567996.1\|997636_997906_+\|type-II-toxin-antitoxin-system-ParD-family-antitoxin	gnl\|CDD\|274227	TIGR02606, Antitoxin_ParD, putative addiction module antidote protein, CC2985 family. This bacterial protein family has a very similar seed alignment to that of pfam03693 but is a more stringent model with higher cutoff scores. Proteins that score above the trusted cutoff to this model almost invariably are found adjacent to a ParE family protein (pfam05016), where ParE is the killing partner of an addiction module for plasmid stabilization. Members of this family, therefore, are putative addiction module antidote proteins. Some are encoded on plasmids or in prophage regions, but others appear chromosomal. A genome may contain several identical copies, such as the four in Magnetococcus sp. MC-1. This family is named for one member, CC2985 of Caulobacter crescentus CB15. [Cellular processes, Other, Mobile and extrachromosomal element functions, Plasmid functions].	1.30837e-05
NZ_CP051167.1\|WP_168568005.1\|1010483_1011416_-\|phosphate/phosphite/phosphonate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|379006	pfam12974, Phosphonate-bd, ABC transporter, phosphonate, periplasmic substrate-binding protein. This is a family of periplasmic proteins which are part of the transport system for alkylphosphonate uptake.	2.40424e-57
NZ_CP051167.1\|WP_168567990.1\|995057_995456_-\|endonuclease-domain-containing-protein	gnl\|CDD\|238509	cd01038, Endonuclease_DUF559, Domain of unknown function, appears to be related to a diverse group of endonucleases.	1.44978e-38
NZ_CP051167.1\|WP_168567995.1\|997145_997457_-\|DUF433-domain-containing-protein	gnl\|CDD\|225291	COG2442, COG2442, Uncharacterized conserved protein [Function unknown].	1.96479e-23
NZ_CP051167.1\|WP_168568002.1\|1007209_1008061_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	2.05317e-115
NZ_CP051167.1\|WP_168571729.1\|993944_994706_+\|peptidylprolyl-isomerase	gnl\|CDD\|275293	TIGR04500, PpiC_rel_mature, putative peptide maturation system protein. Members of this protein family have a novel N-terminal sequence region. Close homologs to the C-terminal region of this protein score well to PpiC-type peptidyl-prolyl cis-trans isomerase models (see pfam00639), yet no sequence within the family scores well to such models, suggesting origin within a branch of the PpiC family but subsequent neofunctionalization with a rapid change of sequence. The genome context for members always includes an ATP-grasp enzyme associated with peptide modification and a short polypeptide likely to be the modification target.	1.94256e-15
NZ_CP051167.1\|WP_168568001.1\|1006374_1007001_-\|SMC-Scp-complex-subunit-ScpB	gnl\|CDD\|213521	TIGR00281, Segregation_and_condensation_protein_B, segregation and condensation protein B. Shown to be required for chromosome segregation and condensation in B. subtilis. [Cellular processes, Cell division, DNA metabolism, Chromosome-associated proteins].	3.15791e-41

>NZ_CP051167.1|WP_168567996.1|997636_997906_+|type-II-toxin-antitoxin-system-ParD-family-antitoxin
MKSINISLPDSMRAYVEEVVAKEGYSTLSEYFRELVRQDQKRKATERLETLLLEGLESGTATAIAPQDWQDIRSAVRERLAKRSQPTED
>NZ_CP051167.1|WP_168567995.1|997145_997457_-|DUF433-domain-containing-protein
MEMVITEHIEITPGVCGGKPRIAGHRIKVQDIVIWYEEMGMSPDEILYHHPSISLADVYAALAYYHDHREEIRRQLREDEAFAREMQAQTPSLLQEKLKHRNA
>NZ_CP051167.1|WP_168567994.1|996817_997153_-|DUF5615-family-PIN-like-protein
MPKTIRFHLDENVSNAIAEGLRRRGIDVTTTPESGLIGVSDEEQIALCREQERVIFTQDTDFLRMAQIGISHRGIIYCQQKTRSIGDIVRGITLIWEYLESEEIQDKVEFI
>NZ_CP051167.1|WP_168567993.1|996453_996831_-|hypothetical-protein
MSLFDEKVQLRGGEEIALWEKEAIAFLGGRSHSGKKGDRPSKKRSHFWEGDRSLMGKGRSLSEKKQGIERQCRGDSRIAPTTNPAFWKTIALCKKGDRTPGKKKRSHSGRAIAFLRFRQFSLTGS
>NZ_CP051167.1|WP_168567992.1|995872_996439_+|Uma2-family-endonuclease
MPEMTIKDVERIESILSDAGLDCQLELEEGRIIIKNPSDLIASEVSVEFASQLSNWVKPRRLGRVFDSAGGFILPNSDLKAPDVSFVLRSRLPRSVRYFATLVPDLVVEVKSQSDRIKKLREKIKVYLEQGVQVAILIDPDTCLVEVYRPDTSVQTLGNGDILTVPELLPEWELVVEELWPVIFEDEE
>NZ_CP051167.1|WP_168567991.1|995511_995847_-|hypothetical-protein
MIYCNKKRAIAVLEKGDRSLGKKRSLSGIKRRSLSGKKAIALWEKEAIAFWDKKAIALWEKGDRISGRAIALNRDVNKLAPLSKGGWGDPTPDRLLVVSPEIPSERRVNLH
>NZ_CP051167.1|WP_168567990.1|995057_995456_-|endonuclease-domain-containing-protein
MTKFTNSQFHLPYNPKLVSIAKQMRQNPTPAEKKLWQDCLRKFPLRILRQRPIDNFIVDFYCASLKLVIGIDGESHFTQQGQDYDEERTRILEGYGITVVRFTNVDVLQNFEGVCRQLERWIPPTPLGKGGF
>NZ_CP051167.1|WP_168567989.1|994780_995002_+|hypothetical-protein
MLPASSLVALPTLQAFNRCDRLFFPECDRLFFPECDRLFIPESDRFFPRERSPFYPRERSPFSSESDRSFSRM
>NZ_CP051167.1|WP_168571729.1|993944_994706_+|peptidylprolyl-isomerase
MDSIPFLTINNQTISLSQAIGYLKASGKFGLFLSEILRQYILTHELDELESIDIALEELEQTILNFRLNNQLLDQNKFQDWLVKNGISYVNFRQRITNDLKLDKLKAKISEPKIEEYFKTQKQFFDRVVLSRIILNDKALAQKLNEELLADPRKFETLAREYSITDDRVVNGMMGPVSRGTLPDILKNPIEFSPVGEIIGPLEIDENYGLFRVEQFLDASLDDPKLKQELQNQLFEQWLQEKLQSLEIKLEVK
>NZ_CP051167.1|WP_168567988.1|989974_993841_+|hypothetical-protein
MRFVGGSVAGTDKISIGAYDGQDWGLQFAIITTQKVNQAPVVTAYNQTVNSGSSTSLSFSVTDPDGDQIRYYYFSDNNSSSTSGYFTVNGVKQTSGFYVDPDKLNTVRFVGGSAAGTDPIRIWAYDGQDWGYKDATMTTQQVNRAPVVTAYDRTVNSGSSNSLSFSASDPDGDRISYYYFSDYNTSSTSGYFTLNGVKQTSSFSVAADNLNTVRFVGGSAAGTDEIRIWAYDGQTWGSNDATITTQQANRAPVVTAYDRTVNSGSSNSLSFSASDPDGDRISYYYFSDYNTSSTSGYFTLNGVKQTSSFSVAADNLNTVRFVGGSAAGTDEIRIWAYDGQTWGSNDATITTQQANRAPVVTAYDRTVNSGSSINPGFYVSDPDGDQITRYYFSDYNTSSTSGYFTLNGVKQTSSFFVDADKLNTVRFVGGSATGTDQIRIWAYDGQTWGSNDATITTQKVNRAPVVTAYNQTVRRNQSIQPSFSVTDADGDTMTRYAFFDGNTSSTSGYFTVNGVKQAAGQTFYVNADQLNTVRFVGGSSNSNDYVYTRAYDGSAWSNWKDYLMKTEGGSKPVVSATDQTVKRNQSIQPSFSVTDADGDTMTRYRFFDGDNSSTSGYFTVNGVKKAAHQTFYVDADQLHTVRFVGGSVAGNDRVYVSATDGLDGWSTWQDYLMKTEGGSKPVVSATDQTVKRNQSIQPSFSVTDADGDTMTRYRFFDGDNSSTSGYFTVNGVKKAAHQTFYVDADQLHTVRFVGGSVAGNDRVYVSATDGIDGWSTWQDYLMKTQSGSNPVVTASDQTVNANESMKLSFSVTDADGDTMTRYAFFDGNSSSTSGYFTVNGVKQAAGQTFYVDADKLDTVRFVGGAVAGIDGLHVRTSDGVDGWSEWTKFNVSTKATVINDWFEQNIKDAAIRSLARSRFQDGELDRKDMIDIFINATDSGVVDAYEFADLQTLTSNKDYIKMPDYVQILSTKISHGNPANKSYRGTYLGNLQAGSSGEHLGKLIKKHFLGQDHPLPKGEYSYGSASNVEYRYAEGQLFQNGISYEDIKQGAVGDCYYLASLAAVAQKTPNVIKDMFIDNGIDEDGNRTYTVRFYNNGQVDYVTVDRYLPTNKNNGSLPFAGVGNGHTYKNSNNELWVALAEKAYAQMNEAGWMKRYTTDEGIDLHGLNSYKGIEGGWTNVSVAHINNQSGTRHSISSSTASSVVTAFNFGKLVNFSSLGKEATHGSPVVSSHAYTMVDYNQSTGKFKLFNPWGLDGGTEPGDSAFKPGILEMSWNEIKTYFRYWRVNG
>NZ_CP051167.1|WP_168567998.1|998830_1000435_-|CHAT-domain-containing-protein
MKIHRILWVIIVTGTGLAIATCPGLTQTGNQSDITGPNMSDITGPDLEDFGFDEEFYEEFDEEFDEEFDEEFDEEFDYFDDEIDRGEYESQLEQLEIDISLEFIEEYQAIEFSDYLGVDLFGEIPSLEEIAKTLYDLWQTTGQKSAFIYVTSRDRSLDIVTVFPDESLSQSLVSSRVKHPEILTNIFTQDRQKQFTQKAIVPDVDRQKLLADVTKFRLQILSPQYRNSQQYLPLSKKLYQLLIAPIEDRLKAENIQNLVFSMDSGLRYLPLAVLHDGEQFLIEKYGVSLVPSFGLTDITYVDIRDRPVLAMGSAKFEGLPALPGVPLEVTNILEIPWMGESFINEQFTLDNFKQQAASQNFGVIHLATHAEFKPGRLENSYIQFFEDKLNLVQFRQLAQELGWTSVENPPIELLVLSACRTALGEEQAELGFAGLAVLSGVKSVLGSLWYVSDAATLGLMSEFYHHLRKTPIKVQALRESQLALLQGKVEVKNGLLYLSTGETLALPPELAQFEGMNFSHPYYWSAFTLIGNWN
>NZ_CP051167.1|WP_168567999.1|1002708_1004658_-|CHAT-domain-containing-protein
MYSLRWFLTPAITSFGVILLSQFPTIAQNQSDVTGPNVDPPLNQSDITGPQPIEISPIDLIEPLETEEPNNIIDETPPVDDAIVDNPNQQQPQNNSTPNNPIDTVPVDNDSDSPGLPVSDGNVVPENPTDFSENPQNNSGEPSIADSTTTTENSSENIDNIDRNNSVHVETSRPIEASILDAFFGDENTELEVDRQRYENLVAQSDIPTTLQLFEEFYALEFSNFLGIELFGKVAQVDEIAAKLYEMWQVTGKKAAFLYISSYEDRLELLLIPPVPPLDGSEITPVSRLKTIPKQQPTIAQGYLEEVISHSERHVIPNLSSEIVSKEIGLFQNAITDPRKRGSSQYLPHAQQLYQWFVDPVNVSLQEKEIDILVLAVNQGLRSVPFSALHDGDRFLIEKYALTLVPSFGLTDISFVDFRNSPILAMGASEFSELNDLPAVPLELEEIANSGLPTDAFLNEGFTVENFLQQNENKQYRGIHIATHAEFRPGALSNSYIYFYNNKIGLDRLRKITDRLGWNLTTTPAIELLTLSACRTALGDPQAELGFAGLAVLYGAKSALASLWYVSDEGTLGLMGEFYNHLQNNPLKSIALQEAQLAMLRGETYSENGLLHFSNGQTTAWEDETKSQQKFDYSHPYYWSAFSLIGNWN
>NZ_CP051167.1|WP_168568000.1|1005035_1005980_-|hypothetical-protein
MKLILTPIAIAVMFCPRAIAIPLDLEREREHFDPEPISIQPLRIGQATPPPDSTPSSSPGSLHRKQGNEQRFQPQRVPFRPRPNQGKPSAAASPGITIMNPSGYGASWGTLGIGLGLQERTRFTEDADGVMGIGMGFGDPRKNVGVALGVTVTDLWGDAFEDGTLSIKLHRRLPADFSVAAGVQGAVRWGETDGGSSVYGVVSRRFALQEDPSKPLSQLFLSVGVGGGQYRTEDQIDDGVDTVGLFGSAALRLYEPVNAVVEWTGQDLTVGLSIAPFRNVPIVISPALTDITGSAGDGTRFILGIGYGFSFDRF
>NZ_CP051167.1|WP_168568001.1|1006374_1007001_-|SMC-Scp-complex-subunit-ScpB
MTRLATTIEAILYLKGKPLSLAEIAEFAQCDKEDAEEALIELMGDYAHRESALEIVESNKGYTLQLRETFQDLVHSLIPAELGVGALRTLAAIALKKGSMSQTELVELRGSGAYQHVQELIQQGFVRRRRQSDGRSYWLQVTDKFHQYFQTEQLPQQLQLPLTSDRDEEAENGLENPSETAPETAPETAPETQATAANPAPVGPLPEG
>NZ_CP051167.1|WP_168568002.1|1007209_1008061_-|ABC-transporter-ATP-binding-protein
MSAAVCVENVRKIYDRTPVVNGLSFAIAPGEMFGLLGPNGAGKSTTIRMLTTLTRPSEGTIQVAGYDVRRDPIAVKQQIGVVLQQTSVDLDLTVWENMEFHGRLHHIPKTERQQRIDRALTYVELSDRQDVKAKTLSGGMKRRLQIARALLHEPKILFLDEPTVGLDPQTRRRLWEIIRDLNRQGMTMLLTTHYMEEVEYLCDRIGIMDAGTLIELGTLDELRHKHGGGLVMKQVGDRWEYKFFPDLDAANAYFEAQPDKTGLMVRPSNLEDIFVELTGRQLD
>NZ_CP051167.1|WP_168568003.1|1008124_1008376_-|TIGR02450-family-Trp-rich-protein
MAKKKQKFPYLVGSKWTARQKTWGWRHFQVVNRKNDGKWVFAEMVASCDPNVRFWLNARQLKDENLWQAGWQTLTEMGQEREG
>NZ_CP051167.1|WP_168568004.1|1008486_1010478_-|HAMP-domain-containing-protein
MGINSHSKGSLATKLTLSMTGLVILVVAGVTGLSLYREQQTFRKELQQQAQILLDALSVTTSDSLYNLDADFMEEIMEQLGADRVLVAGRIYDREGRVVADAYGEDVLVYNVEPDPFGQALLASNRTTFQWEADQLLAGKAVLVGRQRLGAVSVGLSTTPLKEKMAVVRYQGLAVAAAAAIAGTAIALLLSRSITEPLQEMTVATKRLSSGDLSQKIAIRSNDELAVLAESFNRMTDQLRSSIESLEQQTEDLRQSEAKNRALLDAIPDLMFRFSKSGEFVDFKASRNGDLLSNLGNLLGKTLYEVLPTHVAHKYIEHVDRAIASGEIQVFEYEWFLHNQRHHFEARLVVNGGDDVLAIVRDITESKLAQIELEQAKEAAESANHAKSQFLANMSHELRTPLNAILGYSDLLREDAEDLGYNDFVPDLMLIREAGAHLLNIISDVLDISKIEAGEMKIYLERFDIVTLIEEVESTINPLVQKNNNTFELDCPAQMGHMIADRTKVKQVLLNLLSNAAKFTHEGRITLQIKRTPVADSSSEAIAQLPPSPSDNPASDRSPTETNGRLSANPVPQASEWVIFEVADTGIGMTPEQIDKIFQPFIQADISTTKRYGGTGLGLAICQRFCEIMGGELFVTSEIDRGSTFTFRLPDVVRDPQEALTHC
>NZ_CP051167.1|WP_168568005.1|1010483_1011416_-|phosphate/phosphite/phosphonate-ABC-transporter-substrate-binding-protein
MFQKLLKNLMLVGLLATIASCDSQPTQISTDEPTAPPTGKALVIADVSNNPAKKIKRYQPMADYLAKNLSQFDIGIGEVKVAGDLETISSWLKSGEIDIYFDSPYPAMRVSQLSGAQAILRRWKDRTPDYYTIIFTMGDRDINSLEDLKGKTISFDEPNSTSGYMLPAAYLIEAGLNPVEKNSAADTVGENEVGYVFSDDDENTIQWVISGKVAAGALDIGTFEEIPPQSRAAMKVLAETEKVARHIVMVRPDMNPEMVAALKTILLEMDKTPEGKEVLDIFEDTAKFDEFPPEASFQRMRELYEQVENR
>NZ_CP051167.1|WP_168568006.1|1012329_1012503_+|hypothetical-protein
MTPFESLPDNLSLPIAPTTAIERMARSQTGFIRKNPEPSIAPFNLHSRCLFHEGHPQ
>NZ_CP051167.1|WP_168568007.1|1012499_1014275_+|PEP-CTERM-sorting-domain-containing-protein
MKISNSSQTFPHSIGKLLKFSLPSALIWTSLATAANAFDLRPIGTYQTGIFDDSAARITTYDPLSQRLFVTNDSTQRIEILDIFDPTNPYPVAANPFIDLTTLDLGLDFEVGGINSIAFKDGILAAAVESKNLQDPGRVLFFDSNGTLLNSLTVGALPDMLTFTPDGRKILVANEGEPSGDYLNDPEGSVSIIELAADIASLTDANVKTADFKLFNNIAIDDRIRIFGPNATVAQDLEPESIAVSADGTKAWVTLQENNAIAVLDLLTGEFTDLFALGFKDYSQPQNALDPSDRDGGINSRTLQNLFGIYQPDEIASYTFGGQTFLFTANEGDSREYLFEDEAGNEIESLVEETSVGDVLLDPDLFPNAAEIQDNSNFGRLEITNTMGDIDGDGDYDELYAFGGRSFSIWDELGNLIFDSGNEFERITAELFPDDFNSNNDANQSFDNRSDNKGPEPEGITLGRILEKTYAFIGLERIGGIIAYDVTDPYNPFFVDYFNNRNFAALFNEDVFGEDEEPSREQLDAVGDLGPEGLLFIAAADSPTGRPLLAVANEVSGTTTLYSVRVPEPSSAIALAGVGALGWLSRKRKRA

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Crispr_ID: NZ_CP051167_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_4

1029690-1032375

TypeI-D

V-U2:NA

Consensus_repeat	Method
GTTTC---------AATCCCGTTGCCGGGATTCATTGAATTGAAAG	PILER-CR
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CRISPRCasFinder
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CRT
GTTTC---------AATCCCGTTGCCGGGATTCATTGAATTGAAAG	PILER-CR

36 spacers

WYL,cas3,cas10d,csc2gr7,csc1gr5,cas6,cas4,cas1,cas2

The CRISPR arrays of NZ_CP051167_4

>merge|NZ_CP051167|4|1029690-1032375|PILER-CR,CRISPRCasFinder,CRT,PILER-CR
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGGCAGCCCCCCGCCAAGTTTGGCAATGCATATCGAGAGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGCCAAAGAGGAGCAGCGACTATCTATCGCCGTAAAGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGGATTCGGATGGGGATTACCTCATCCCTACCGGGGGGGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGCCTTTAAGGAAAGTAATCGGAACTGTCTCCGGCCTGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGCCTTTGAAAAAAGCAATGGGACTATTAAAGCTATTGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGACGGCGCCGACCTGCGTGGATCCAGCTTAAAAGGTGTTGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGAACCTAATTGGCGCTAACCTCAATGGCGCCACTCTCTACGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTCCTCGGATCTTCTCCAAGGAAACAAATGCTTCCCGAGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGGGGGCCAATCTCCGGGGTGTAAATCTCGAAATTTCCGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTCCGTCGTGGCTGTAAAGCCCGTTACCTGGTAGTTGGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGCGACCTTTATCTCCCCTGTATACCCTTCGTCGATGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTTCGTCATTTATTGAGTGCTGCAAAGAAAGCTCGGGGTTGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGATCGAATGGTATAATTCCGTCCTCCGGGGACGGGGGTGGACGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGCTTCGATAGCCGCCTCGGGGAGCAGCTAGAGGCTCGGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGAGATCCGCCAGCTTCGAGCTGCCGCCAAGGCTAAAGCGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGCCCCTAAGGTAAGCAGGCGAAAAGGCAAAGGAGGGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTTGAGAGAAATAATAATGGAACGCGGAAATGATATAGGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGAGCAACACCTGGGGCGAAATTAGAGATGGCGGAGGCGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGCTTGTCTTCCCATTGCCCCCAATAGGCGATTTTTGGGGAGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTCCCCGTTCGGATGGCTGTATACTCCCCTGGGTTTAGGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGGCCCCGACATGTACGGCGCGGGGCGATAGGCGGTTCGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGACGAATCAAAGCATTTTTCGGCTGGTTTACTTCCTCACAAGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGCTGAGTCGCACTGGTCGGGACCTTGAAGAAATTCTTGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGATACCTTGACTCGTAAGGTCTCGGTTTTGAAGTGAGGCGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTCTATACGTTCTAATCGATAGTTCGGGTTCTATGGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGCTGTAGCTCCCCGATAAAATTCTTGCAGGCCGTGAGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGAACCTTAGCGGTGCCAATTTAGAGGGTGCCGACCTCGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTCCTAAGAAGTCATCAAGTACAATCATTTAATTGAATGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTCTAGTCCTCTAGGGGTTTGTACCCTTATTAGTAATAGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTTCTACAGGTCGCATTTCTCGCAGCCTTGAGGGCATGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTCCGATAGCTGTCTCTGGGTAAGACCTAAGGACTGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTCGGCGAGGCGCTCGTCGGCAGCGATCGCCCGCCAGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTCGCGTTCCGACGAGGGCGCGATCGGCGATCCTTGTGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGCCACTGAGTTAATCAGTGGGGATTTTCGGGGCTATTCGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGGAAAGGTAAAGGAGGTTCTCCGGCCTTCCTCGATTGCTCGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTCCAGTCTGGTCACCAGACTGTGACGTCTGCTTGCTGTTGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG

>NZ_CP051167|4|2|1029690-1031048|PILER-CR
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GCAGCCCCCCGCCAAGTTTGGCAATGCATATCGAGA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCAAAGAGGAGCAGCGACTATCTATCGCCGTAAA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GATTCGGATGGGGATTACCTCATCCCTACCGGGGGG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCTTTAAGGAAAGTAATCGGAACTGTCTCCGGCCT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCTTTGAAAAAAGCAATGGGACTATTAAAGCTATT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ACGGCGCCGACCTGCGTGGATCCAGCTTAAAAGGTGTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AACCTAATTGGCGCTAACCTCAATGGCGCCACTCTCTAC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCTCGGATCTTCTCCAAGGAAACAAATGCTTCCCGA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GGGGCCAATCTCCGGGGTGTAAATCTCGAAATTTCC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCGTCGTGGCTGTAAAGCCCGTTACCTGGTAGTTG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CGACCTTTATCTCCCCTGTATACCCTTCGTCGAT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TTCGTCATTTATTGAGTGCTGCAAAGAAAGCTCGGGGTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ATCGAATGGTATAATTCCGTCCTCCGGGGACGGGGGTGGAC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CTTCGATAGCCGCCTCGGGGAGCAGCTAGAGGCTCG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AGATCCGCCAGCTTCGAGCTGCCGCCAAGGCTAAAGC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCCCTAAGGTAAGCAGGCGAAAAGGCAAAGGAGG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TTGAGAGAAATAATAATGGAACGCGGAAATGATATAG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AGCAACACCTGGGGCGAAATTAGAGATGGCGGAGGC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGCTTGTCTTCCCATTGCCCCCAATAGGCGATTTTTGGGGAGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTCCCCGTTCGGATGGCTGTATACTCCCCTGGGTTTAGGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GCCCCGACATGTACGGCGCGGGGCGATAGGCGGTTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ACGAATCAAAGCATTTTTCGGCTGGTTTACTTCCTCACAA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CTGAGTCGCACTGGTCGGGACCTTGAAGAAATTCTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ATACCTTGACTCGTAAGGTCTCGGTTTTGAAGTGAGGC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCTATACGTTCTAATCGATAGTTCGGGTTCTATG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CTGTAGCTCCCCGATAAAATTCTTGCAGGCCGTGA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AACCTTAGCGGTGCCAATTTAGAGGGTGCCGACCTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCTAAGAAGTCATCAAGTACAATCATTTAATTGAAT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCTAGTCCTCTAGGGGTTTGTACCCTTATTAGTAATA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TTCTACAGGTCGCATTTCTCGCAGCCTTGAGGGCAT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCGATAGCTGTCTCTGGGTAAGACCTAAGGACT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCGGCGAGGCGCTCGTCGGCAGCGATCGCCCGCCA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCGCGTTCCGACGAGGGCGCGATCGGCGATCCTTGT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCACTGAGTTAATCAGTGGGGATTTTCGGGGCTATTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GAAAGGTAAAGGAGGTTCTCCGGCCTTCCTCGATTGCTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCAGTCTGGTCACCAGACTGTGACGTCTGCTTGCTGTT


>NZ_CP051167|4|3|1029690-1032375|CRISPRCasFinder
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GCAGCCCCCCGCCAAGTTTGGCAATGCATATCGAGA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCAAAGAGGAGCAGCGACTATCTATCGCCGTAAA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GATTCGGATGGGGATTACCTCATCCCTACCGGGGGG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCTTTAAGGAAAGTAATCGGAACTGTCTCCGGCCT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCTTTGAAAAAAGCAATGGGACTATTAAAGCTATT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ACGGCGCCGACCTGCGTGGATCCAGCTTAAAAGGTGTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AACCTAATTGGCGCTAACCTCAATGGCGCCACTCTCTAC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCTCGGATCTTCTCCAAGGAAACAAATGCTTCCCGA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GGGGCCAATCTCCGGGGTGTAAATCTCGAAATTTCC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCGTCGTGGCTGTAAAGCCCGTTACCTGGTAGTTG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CGACCTTTATCTCCCCTGTATACCCTTCGTCGAT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TTCGTCATTTATTGAGTGCTGCAAAGAAAGCTCGGGGTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ATCGAATGGTATAATTCCGTCCTCCGGGGACGGGGGTGGAC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CTTCGATAGCCGCCTCGGGGAGCAGCTAGAGGCTCG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AGATCCGCCAGCTTCGAGCTGCCGCCAAGGCTAAAGC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCCCTAAGGTAAGCAGGCGAAAAGGCAAAGGAGG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TTGAGAGAAATAATAATGGAACGCGGAAATGATATAG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AGCAACACCTGGGGCGAAATTAGAGATGGCGGAGGC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CTTGTCTTCCCATTGCCCCCAATAGGCGATTTTTGGGGA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCCCGTTCGGATGGCTGTATACTCCCCTGGGTTTAG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GCCCCGACATGTACGGCGCGGGGCGATAGGCGGTTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ACGAATCAAAGCATTTTTCGGCTGGTTTACTTCCTCACAA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CTGAGTCGCACTGGTCGGGACCTTGAAGAAATTCTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ATACCTTGACTCGTAAGGTCTCGGTTTTGAAGTGAGGC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCTATACGTTCTAATCGATAGTTCGGGTTCTATG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CTGTAGCTCCCCGATAAAATTCTTGCAGGCCGTGA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AACCTTAGCGGTGCCAATTTAGAGGGTGCCGACCTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCTAAGAAGTCATCAAGTACAATCATTTAATTGAAT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCTAGTCCTCTAGGGGTTTGTACCCTTATTAGTAATA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TTCTACAGGTCGCATTTCTCGCAGCCTTGAGGGCAT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCGATAGCTGTCTCTGGGTAAGACCTAAGGACT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCGGCGAGGCGCTCGTCGGCAGCGATCGCCCGCCA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCGCGTTCCGACGAGGGCGCGATCGGCGATCCTTGT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCACTGAGTTAATCAGTGGGGATTTTCGGGGCTATTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GAAAGGTAAAGGAGGTTCTCCGGCCTTCCTCGATTGCTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCAGTCTGGTCACCAGACTGTGACGTCTGCTTGCTGTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG

>NZ_CP051167|4|1|1029690-1032375|CRT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GCAGCCCCCCGCCAAGTTTGGCAATGCATATCGAGA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCAAAGAGGAGCAGCGACTATCTATCGCCGTAAA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GATTCGGATGGGGATTACCTCATCCCTACCGGGGGG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCTTTAAGGAAAGTAATCGGAACTGTCTCCGGCCT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCTTTGAAAAAAGCAATGGGACTATTAAAGCTATT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ACGGCGCCGACCTGCGTGGATCCAGCTTAAAAGGTGTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AACCTAATTGGCGCTAACCTCAATGGCGCCACTCTCTAC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCTCGGATCTTCTCCAAGGAAACAAATGCTTCCCGA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GGGGCCAATCTCCGGGGTGTAAATCTCGAAATTTCC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCGTCGTGGCTGTAAAGCCCGTTACCTGGTAGTTG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CGACCTTTATCTCCCCTGTATACCCTTCGTCGAT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TTCGTCATTTATTGAGTGCTGCAAAGAAAGCTCGGGGTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ATCGAATGGTATAATTCCGTCCTCCGGGGACGGGGGTGGAC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CTTCGATAGCCGCCTCGGGGAGCAGCTAGAGGCTCG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AGATCCGCCAGCTTCGAGCTGCCGCCAAGGCTAAAGC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCCCTAAGGTAAGCAGGCGAAAAGGCAAAGGAGG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TTGAGAGAAATAATAATGGAACGCGGAAATGATATAG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AGCAACACCTGGGGCGAAATTAGAGATGGCGGAGGC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CTTGTCTTCCCATTGCCCCCAATAGGCGATTTTTGGGGA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCCCGTTCGGATGGCTGTATACTCCCCTGGGTTTAG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GCCCCGACATGTACGGCGCGGGGCGATAGGCGGTTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ACGAATCAAAGCATTTTTCGGCTGGTTTACTTCCTCACAA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CTGAGTCGCACTGGTCGGGACCTTGAAGAAATTCTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ATACCTTGACTCGTAAGGTCTCGGTTTTGAAGTGAGGC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCTATACGTTCTAATCGATAGTTCGGGTTCTATG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CTGTAGCTCCCCGATAAAATTCTTGCAGGCCGTGA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AACCTTAGCGGTGCCAATTTAGAGGGTGCCGACCTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCTAAGAAGTCATCAAGTACAATCATTTAATTGAAT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCTAGTCCTCTAGGGGTTTGTACCCTTATTAGTAATA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TTCTACAGGTCGCATTTCTCGCAGCCTTGAGGGCAT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCGATAGCTGTCTCTGGGTAAGACCTAAGGACT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCGGCGAGGCGCTCGTCGGCAGCGATCGCCCGCCA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCGCGTTCCGACGAGGGCGCGATCGGCGATCCTTGT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCACTGAGTTAATCAGTGGGGATTTTCGGGGCTATTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GAAAGGTAAAGGAGGTTCTCCGGCCTTCCTCGATTGCTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCAGTCTGGTCACCAGACTGTGACGTCTGCTTGCTGTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG

>NZ_CP051167|4|3|1031162-1032375|PILER-CR
	GCAGCCCCCCGCCAAGTTTGGCAATGCATATCGAGA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCAAAGAGGAGCAGCGACTATCTATCGCCGTAAA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GATTCGGATGGGGATTACCTCATCCCTACCGGGGGG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCTTTAAGGAAAGTAATCGGAACTGTCTCCGGCCT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCTTTGAAAAAAGCAATGGGACTATTAAAGCTATT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ACGGCGCCGACCTGCGTGGATCCAGCTTAAAAGGTGTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AACCTAATTGGCGCTAACCTCAATGGCGCCACTCTCTAC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCTCGGATCTTCTCCAAGGAAACAAATGCTTCCCGA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GGGGCCAATCTCCGGGGTGTAAATCTCGAAATTTCC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCGTCGTGGCTGTAAAGCCCGTTACCTGGTAGTTG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CGACCTTTATCTCCCCTGTATACCCTTCGTCGAT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TTCGTCATTTATTGAGTGCTGCAAAGAAAGCTCGGGGTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ATCGAATGGTATAATTCCGTCCTCCGGGGACGGGGGTGGAC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CTTCGATAGCCGCCTCGGGGAGCAGCTAGAGGCTCG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AGATCCGCCAGCTTCGAGCTGCCGCCAAGGCTAAAGC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCCCTAAGGTAAGCAGGCGAAAAGGCAAAGGAGG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TTGAGAGAAATAATAATGGAACGCGGAAATGATATAG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AGCAACACCTGGGGCGAAATTAGAGATGGCGGAGGC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGCTTGTCTTCCCATTGCCCCCAATAGGCGATTTTTGGGGAGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAGTCCCCGTTCGGATGGCTGTATACTCCCCTGGGTTTAGGTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GCCCCGACATGTACGGCGCGGGGCGATAGGCGGTTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ACGAATCAAAGCATTTTTCGGCTGGTTTACTTCCTCACAA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CTGAGTCGCACTGGTCGGGACCTTGAAGAAATTCTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	ATACCTTGACTCGTAAGGTCTCGGTTTTGAAGTGAGGC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCTATACGTTCTAATCGATAGTTCGGGTTCTATG
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CTGTAGCTCCCCGATAAAATTCTTGCAGGCCGTGA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	AACCTTAGCGGTGCCAATTTAGAGGGTGCCGACCTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCTAAGAAGTCATCAAGTACAATCATTTAATTGAAT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCTAGTCCTCTAGGGGTTTGTACCCTTATTAGTAATA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TTCTACAGGTCGCATTTCTCGCAGCCTTGAGGGCAT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCGATAGCTGTCTCTGGGTAAGACCTAAGGACT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCGGCGAGGCGCTCGTCGGCAGCGATCGCCCGCCA
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCGCGTTCCGACGAGGGCGCGATCGGCGATCCTTGT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	CCACTGAGTTAATCAGTGGGGATTTTCGGGGCTATTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	GAAAGGTAAAGGAGGTTCTCCGGCCTTCCTCGATTGCTC
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG	TCCAGTCTGGTCACCAGACTGTGACGTCTGCTTGCTGTT
GTTTCAATCCCGTTGCCGGGATTCATTGAATTGAAAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168568015.1\|1025469_1025682_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568024.1\|1040773_1041622_+\|CRISPR-system-precrRNA-processing-endoribonuclease-RAMP-protein-Cas6	cas6	pfam10040_cas6_CAS-III:CAS-IV	gnl\|CDD\|227838
NZ_CP051167.1\|WP_168568013.1\|1020539_1024370_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568020.1\|1033800_1035924_+\|type-I-D-CRISPR-associated-helicase-Cas3'	cas3	cd09710_cas3_CAS-I-D	gnl\|CDD\|187841
NZ_CP051167.1\|WP_168568027.1\|1049764_1050976_-\|amidohydrolase	unknown	unknown	gnl\|CDD\|349941
NZ_CP051167.1\|WP_168568009.1\|1016356_1017244_-\|ROK-family-protein	unknown	unknown	gnl\|CDD\|224851
NZ_CP051167.1\|WP_168568016.1\|1025975_1028420_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|236137
NZ_CP051167.1\|WP_168568019.1\|1032607_1033582_-\|WYL-domain-containing-protein	WYL	pfam13280_WYL_CAS-I:CAS-III	gnl\|CDD\|379100
NZ_CP051167.1\|WP_168568023.1\|1040007_1040784_+\|type-I-D-CRISPR-associated-protein-Cas5/Csc1	csc1gr5	cd09711_csc1gr5_CAS-I-D	gnl\|CDD\|274458
NZ_CP051167.1\|WP_168568022.1\|1038930_1039929_+\|type-I-D-CRISPR-associated-protein-Cas7/Csc2	csc2gr7	cd09709_csc2gr7_CAS-I-D	gnl\|CDD\|375747
NZ_CP051167.1\|WP_168568011.1\|1018450_1019818_-\|thioredoxin-disulfide-reductase	unknown	unknown	gnl\|CDD\|273540
NZ_CP051167.1\|WP_168568017.1\|1028471_1028867_-\|RidA-family-protein	unknown	unknown	gnl\|CDD\|100011
NZ_CP051167.1\|WP_168568010.1\|1017376_1018258_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224094
NZ_CP051167.1\|WP_168568012.1\|1019930_1020515_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|270691
NZ_CP051167.1\|WP_168568026.1\|1043715_1044009_+\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP051167.1\|WP_168568021.1\|1035934_1038868_+\|type-I-D-CRISPR-associated-protein-Cas10d/Csc3	cas10d	cd09712_cas10d_CAS-I-D	gnl\|CDD\|187843
NZ_CP051167.1\|WP_168571731.1\|1042133_1042715_+\|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	gnl\|CDD\|273040
NZ_CP051167.1\|WP_168568018.1\|1028921_1029608_-\|SAM-dependent-methyltransferase	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568014.1\|1024630_1025497_+\|DUF1664-domain-containing-protein	unknown	unknown	gnl\|CDD\|274008
NZ_CP051167.1\|WP_168568025.1\|1042741_1043719_+\|type-I-D-CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|274976

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168568024.1\|1040773_1041622_+\|CRISPR-system-precrRNA-processing-endoribonuclease-RAMP-protein-Cas6	gnl\|CDD\|227838	COG5551, COG5551, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	5.98446e-12
NZ_CP051167.1\|WP_168568020.1\|1033800_1035924_+\|type-I-D-CRISPR-associated-helicase-Cas3'	gnl\|CDD\|187841	cd09710, Cas3_I-D, CRISPR/Cas system-associated protein Cas3; Distinct diverged subfamily of Cas3 helicase domain. 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; Diverged DNA helicase Cas3'; signature gene for Type I and subtype I-D.	2.72936e-55
NZ_CP051167.1\|WP_168568027.1\|1049764_1050976_-\|amidohydrolase	gnl\|CDD\|349941	cd08021, M20_Acy1_YhaA-like, M20 Peptidase aminoacylase 1 subfamily, includes Bacillus subtilis YhaA and Staphylococcus aureus amidohydrolase, SACOL0085. Peptidase M20 family, uncharacterized subfamily of bacterial proteins predicted as putative amidohydrolases or hippurate hydrolases. These are a class of zinc binding homodimeric enzymes involved in hydrolysis of N-acetylated proteins. N-terminal acetylation of proteins is a widespread and highly conserved process that is involved in protection and stability of proteins. Several types of aminoacylases can be distinguished on the basis of substrate specificity. Aminoacylase 1 (ACY1) breaks down cytosolic aliphatic N-acyl-alpha-amino acids (except L-aspartate), especially N-acetyl-methionine and acetyl-glutamate into L-amino acids and an acyl group. However, ACY1 can also catalyze the reverse reaction, the synthesis of acetylated amino acids. ACY1 may also play a role in xenobiotic bioactivation as well as the inter-organ processing of amino acid-conjugated xenobiotic derivatives (S-substituted-N-acetyl-L-cysteine). This family includes Staphylococcus aureus amidohydrolase, SACOL0085, which contains two manganese ions in the active site, and forms a homotetramer with variations in interdomain orientation which possibly plays a role in the regulation of catalytic activity.	0
NZ_CP051167.1\|WP_168568009.1\|1016356_1017244_-\|ROK-family-protein	gnl\|CDD\|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	7.52523e-69
NZ_CP051167.1\|WP_168568016.1\|1025975_1028420_+\|hypothetical-protein	gnl\|CDD\|236137	PRK07956, ligA, NAD-dependent DNA ligase LigA; Validated.	4.15455e-77
NZ_CP051167.1\|WP_168568019.1\|1032607_1033582_-\|WYL-domain-containing-protein	gnl\|CDD\|379100	pfam13280, WYL, WYL domain. WYL is a Sm-like SH3 beta-barrel fold containing domain. It is a member of the WYL-like superfamily, named for three conserved amino acids found in a subset of the superfamily. However, these residues are not strongly conserved throughout the family. Rather, the conservation pattern includes four basic residues and a position often occupied by a cysteine, which are predicted to line a ligand-binding groove typical of the Sm-like SH3 beta-barrels. A WYL domain protein (sll7009) is a negative regulator of the I-D CRISPR-Cas system in Synechocystis sp. It is predicted to be a ligand-sensing domain that could bind negatively charged ligands, such as nucleotides or nucleic acid fragments, to regulate CRISPR-Cas and other defense systems such as the abortive infection AbiG system.	1.32308e-15
NZ_CP051167.1\|WP_168568023.1\|1040007_1040784_+\|type-I-D-CRISPR-associated-protein-Cas5/Csc1	gnl\|CDD\|274458	TIGR03159, cas_Csc1, CRISPR type I-D/CYANO-associated protein Csc1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) is a widespread family of prokaryotic direct repeats with spacers of unique sequence between consecutive repeats. This protein family is a CRISPR-associated (Cas) family strictly associated with the Cyano subtype of CRISPR/Cas locus, found in several species of Cyanobacteria and several archaeal species. This family is designated Csc1 for CRISPR/Cas Subtype Cyano protein 1, as it is often the first gene upstream of the core cas genes, cas3-cas4-cas1-cas2.	2.75163e-56
NZ_CP051167.1\|WP_168568022.1\|1038930_1039929_+\|type-I-D-CRISPR-associated-protein-Cas7/Csc2	gnl\|CDD\|375747	pfam18320, Csc2, Csc2 Crispr. The Csc2 Crispr family of proteins forms a core RNA recognition motif-like domain, flanked by three peripheral insertion domains: a lid domain, a Zinc-binding domain and a helical domain. The CRISPR-Cas system is possibly a mechanism of defence against invading pathogens and plasmids that functions analogously to the RNA interference (RNAi) systems in eukaryotes.	2.41352e-176
NZ_CP051167.1\|WP_168568011.1\|1018450_1019818_-\|thioredoxin-disulfide-reductase	gnl\|CDD\|273540	TIGR01292, Thioredoxin_reductase, thioredoxin-disulfide reductase. This model describes thioredoxin-disulfide reductase, a member of the pyridine nucleotide-disulphide oxidoreductases (pfam00070). [Energy metabolism, Electron transport].	8.28715e-152
NZ_CP051167.1\|WP_168568017.1\|1028471_1028867_-\|RidA-family-protein	gnl\|CDD\|100011	cd06154, YjgF_YER057c_UK114_like_6, This group of proteins belong to a large family of YjgF/YER057c/UK114-like proteins present in bacteria, archaea, and eukaryotes with no definitive function. The conserved domain is similar in structure to chorismate mutase but there is no sequence similarity and no functional connection. Members of this family have been implicated in isoleucine (Yeo7, Ibm1, aldR) and purine (YjgF) biosynthesis, as well as threonine anaerobic degradation (tdcF) and mitochondrial DNA maintenance (Ibm1). This domain homotrimerizes forming a distinct intersubunit cavity that may serve as a small molecule binding site.	1.8995e-53
NZ_CP051167.1\|WP_168568010.1\|1017376_1018258_-\|ABC-transporter-permease	gnl\|CDD\|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.44798e-78
NZ_CP051167.1\|WP_168568012.1\|1019930_1020515_-\|hypothetical-protein	gnl\|CDD\|270691	cd05121, ABC1_ADCK3-like, Activator of bc1 complex (ABC1) kinases (also called aarF domain containing kinase 3) and similar proteins. This family is composed of the atypical yeast protein kinase Abc1p, its human homolog ADCK3 (also called CABC1), and similar proteins. Abc1p (also called Coq8p) is required for the biosynthesis of Coenzyme Q (ubiquinone or Q), which is an essential lipid component in respiratory electron and proton transport. It is necessary for the formation of a multi-subunit Q-biosynthetic complex and may also function in the regulation of Q synthesis. Human ADCK3 is able to rescue defects in Q synthesis and the phosphorylation state of Coq proteins in yeast Abc1 (or Coq8) mutants. Mutations in ADCK3 cause progressive cerebellar ataxia and atrophy due to Q10 deficiency. Eukaryotes contain at least two more ABC1/ADCK3-like proteins: in humans, these are the putative atypical protein kinases named ADCK1 and ADCK2. In algae and higher plants, ABC1 kinases have proliferated to more than 15 subfamilies, most of which are located in plastids or mitochondria. Eight of these plant ABC1 kinase subfamilies (ABC1K1-8) are specific for photosynthetic organisms. ABC1 kinases are not related to the ATP-binding cassette (ABC) membrane transporter family.	0.000810527
NZ_CP051167.1\|WP_168568026.1\|1043715_1044009_+\|CRISPR-associated-endonuclease-Cas2	gnl\|CDD\|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	1.37382e-24
NZ_CP051167.1\|WP_168568021.1\|1035934_1038868_+\|type-I-D-CRISPR-associated-protein-Cas10d/Csc3	gnl\|CDD\|187843	cd09712, Cas10d_I-D, CRISPR/Cas system-associated protein Cas10d. 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; Large proteins, some contain Zn-finger domain. Fused to N-terminal HD domain; signature gene for I-D subtype; also known as Csc3 family.	0
NZ_CP051167.1\|WP_168571731.1\|1042133_1042715_+\|CRISPR-associated-protein-Cas4	gnl\|CDD\|273040	TIGR00372, conserved_hypothetical_protein, CRISPR-associated protein Cas4. This model represents a family of proteins associated with CRISPR repeats in a wide set of prokaryotic genomes. This scope of this model has been broadened since it was first built to describe an archaeal subset only. The function of the protein is undefined. Distantly related proteins, excluded from this model, include ORFs from Mycobacteriophage D29 and Sulfolobus islandicus filamentous virus and a region of the Schizosaccharomyces pombe DNA replication helicase Dna2p.	7.43662e-31
NZ_CP051167.1\|WP_168568014.1\|1024630_1025497_+\|DUF1664-domain-containing-protein	gnl\|CDD\|274008	TIGR02168, Chromosome_partition_protein_Smc, chromosome segregation protein SMC, common bacterial type. SMC (structural maintenance of chromosomes) proteins bind DNA and act in organizing and segregating chromosomes for partition. SMC proteins are found in bacteria, archaea, and eukaryotes. This family represents the SMC protein of most bacteria. The smc gene is often associated with scpB (TIGR00281) and scpA genes, where scp stands for segregation and condensation protein. SMC was shown (in Caulobacter crescentus) to be induced early in S phase but present and bound to DNA throughout the cell cycle. [Cellular processes, Cell division, DNA metabolism, Chromosome-associated proteins].	0.00317122
NZ_CP051167.1\|WP_168568025.1\|1042741_1043719_+\|type-I-D-CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|274976	TIGR04093, hypothetical_protein_L8106_25395, CRISPR-associated endonuclease Cas1, subtype CYANO. 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 a clade of Cas1 limited to the CYANO subtype of CRISPR/Cas system and most often the type found there.	7.40881e-150

>NZ_CP051167.1|WP_168568018.1|1028921_1029608_-|SAM-dependent-methyltransferase
MGLRLEKVVPWGRSFDEYRRMFALSDDDLDRRILDCAGGPAAFNAAMNRRGTPIVSCDPVYQFSAAEIARRIDETYPVIVRGVAEDRDRYVWGDIHSPEHLGEVRLAAMQQFLADFEQGLRERRYIAAELPNLPFNPGQFDLALCSHFLFSYSVPLSWDFHRAAIAQLCEIAREVRLFPLLDNHSGQTSIHLDPAIAYLQDGGYHVEICPVNYQFQQGGDRMLRITHP
>NZ_CP051167.1|WP_168568017.1|1028471_1028867_-|RidA-family-protein
MQIHRIHSGAPWESQVGYCRAIRAGDRLFVSGTAPIDESGAVFAPGDAYAQAKRCLEIIQQAVRELGGVGAIVVRTRLFVTDIGRWAEYGRAHGEFFCENPPVTTMVEVRSLIDPEMLVEIEAEAIVPAAD
>NZ_CP051167.1|WP_168568016.1|1025975_1028420_+|hypothetical-protein
MTSENHPEAIRTEVEAVTIRVETNGILTPIAQVRAVECGDRSISQATVGGSDRLAALDLHLGDTVVIDAKNPEAIPEIVGVEAEKRPAQAKRVSLPNRCPECGSPTIALEGDDRMRCTNSSCPALLPTILRNWTHREAMDISGMGEKLVQQSIDRGLVSSIADLYDLTVDRLVELERMGQKSAKKLVKSIAKSKSLPWSRILYGLGIRNVGRHAAQSLAHAFPTVRELAHAEPEAIAAIDRLTPETASAIYYWFRIRANQELILALAKAGLQLTEVELPEAIVPSPEAEPEVQPEPEAKAEPEVQPEVQPEPEPEPEPEAEPEVQPEVQPEPEAKAEPEVQPEVQPEPEVQPEPEAEPAASEELSSLQGELAATIADRDRLDAALSDSQTQLQQVRAQRSSLQAELAKSQQAHSELQTQLDELRTRSQAGEGETARLQAQLQTQVQEASDRAAELQGEIDRLQAQLQDRDRQGSQLGSELDRVRAQLNETQGEKSQLQEQVDRLRELCRRLESEKSELQGQLDGAGQQQAQLQEQIDRLESEKSELQGQLDGAGQQQAQLQELCRRLESEKSELQGERDRALTQIQEASDAKAQLESQLAQTRTQLEQVEGQRSQLDAELAAVKTAQTQVDSQLEAARSQLAQIEQERANLQSQLGETRAQLQQTEQAQSELQSQLEQTRTQLEQVRETPSQLQEQIDRLQGQLEESGRKNADLDSHLAQSHAAQSDLQSQLSQVQDKLQQVQQERTQLQERLKQYESDRTTAESQMVSYTEERSQLAKQLEQAQSQGKLLKIAVLLAFGFGSAISWFLSLAIA
>NZ_CP051167.1|WP_168568015.1|1025469_1025682_+|hypothetical-protein
MVGEQNERMSAIAILLDRRFRVRLRLRNLNPTPGLHCDRPPENTGQHRTTPNIDSQPSGELTFCQRSIAK
>NZ_CP051167.1|WP_168568014.1|1024630_1025497_+|DUF1664-domain-containing-protein
MRVREYLQQSQRILRQQHPLALAEYSSIFCSAVGTAIAVLLREVAYATFPLTVALAFNVANRQRLDRDRQEQMTHYFSQVNTRLSEVTPTIAPPPQPPIERPTNELQEELAKLQLCITILESKTNFLNTKLQEKLSSELSAIRQDINAFTEPFNLDNIERKIQSLNSAVQSLLERPLPEWRQYEQLKQSIGQMETNQRELIWPQIKQLNADLESLKKNERHLNQKLDNLLAKFNARPEVPQLSRLKRTVHQLSDRLSQVQQTEVFAKLFDEIEQLNRKVEWLANKMNE
>NZ_CP051167.1|WP_168568013.1|1020539_1024370_-|hypothetical-protein
MAYQKLQKPGSRTPIPQAVKPSSFHKPATDAETEAIAVSSATSEALPEFTPLPANWAQTHPLMRSMEAPESGDRDPTPDVEVAVNPLLTRAAAPSVAGDRSATPSVPTQLIQRDDEDASEDRAADKAEAIYDALNWWDDEEAALAALSGHDSAMRSRIANAFAREHGFSLRSYLKDQLGGDDLVRAIALLDASHTHDPHTAIALALIPLGTRDAEIFRILEGLSLAGRQELETRYNRSFRDIGSGSLKNDLKDDLSGWREQKSLALLHRDLTSADHLYFDSVAITGTHTDSVVSRIQREWQNPANFANFENDWNRYVRNQSGWSDETWTDETLYQAMDGELSGDEWGLVKAVLDGYEAYKRGEAAAESTADPGERQRRLEDVRLQVAEDSLTAATKGAGTNESEVFRAVTEIRQIYQGRIDRARQAGDAEGQAEAERAWEDRRTRLMPFIEGEMYAEGHEYQRVRLLTMGNLDIADEVYLAGEAHDNDRVVTLVTDAWAKGNIGQLIDRAADPKTDETGQIVRPSFRIGFVIPITRGAIWSRMMTLVNTDYDEIGRGANRLKLELDQGDSDSDLKKAYDFLKHKDLNATRRNAVIDRFAAQNLGDEGGGSGIDRFVAYIFRRYESSHTCYEFQDLLQPTADPQEMTTRARGRQEASETGVMNTALNVFVGAYDVVSGEDTAEVVGESADRLEFIAAQAGARPDELEAILAITGARDAQALASLEYTAFRARLDELRSLQRSIAEAIATTVELVVEAALTIATGGAAAGALLASLSSAVAGMLVREMLLGQDYDVLSGENAQKLVTAIASHGFNSVGRGAIDDVLNPERLRQLSRAETFLADAASEAFTQVNLQVVTAGFEGKFPTAESIGAAALSAIGNTAGAGTRGLLGHGLDAQQMARVQRLRHSAVQNITQQVISGVSEEGAALIRTGTGNLTVVDLASRFASRTAQSVGRGLTNSVGEVGGQAVATRRETRRHEAAEMEDGGEPGRDLSEAAARPPVTGEEVAGAAAGVPRSPGSEEGGNLEQVQAARSAIEDLQLPEATVMMPPERRSLSLDEQVRYIGDAQTMYENTWREDPSREAAIYRNSETGEYIIIQGDSGEVYVEGSGGEREAPEGGGVSQRWKELLDGQDVGHWVLMAHSHPVDPTTGVVSDVNRFPSGASGDFQTVFWASQMAGGEARSSTIHYKTPQGPNYTRFGYDPQADSPYWIEVPDPETGRRQRQEFADLEGYHAWMRDRFNVDLGEVPDAMRSPGGDEWDEDTIPDATLPEVTTPRS
>NZ_CP051167.1|WP_168568012.1|1019930_1020515_-|hypothetical-protein
MGDRLSSSGWAGSLASRGPQYGVFAATMPDGTEVVVKVYPPELADKFNEELVGARAASQTSVGARFYGLVDVGPNRLAFAMERVAGGFADAPHGATPEQESEASHYASRVSDRTLADIDTYSQELLDLGYYASGEVQGSIDDSGRWRPIDLQGIDRLSSDPVEAQEQRDEHASNIGMERRHLERLRDRHRGHNP
>NZ_CP051167.1|WP_168568011.1|1018450_1019818_-|thioredoxin-disulfide-reductase
MATPNVENLVIIGSGPAGFTAAIYAARANLKPVVFEGYQMGGLPGGQLMTTTEVENFPGFPEGITGPKLMERMKAQAERWGAELYTEDVTSVDLSQRPFTVRSDEREFKTHSIVIATGATAKRLHLPNEDKFWNNGISACAICDGASPIFKNVELAVIGGGDTAAEESVYLTKYASHVHLLVRRDEMRASKAMQDRVLRNPKLTVHWNTEAVGVFGQEGGQMEGVEIVNNQTGEKSQLKVRGLFYAIGHTPNTQIFKGQIDLDEKGYIVTKPDSVETNVTGVYAVGDVQDHEFRQAVTAAGSGCMGAMLAERWLAEEGLAQEFHQTEESEKPPEPEKEVQADTEATFNPEETRHVGSYALRKLYHESDRLLMVKYVSPTCGPCHTLKPILNKVVDEFEGRIHFVEIDIEQDPEIADNAGVTGTPTIQFFKDKGLVGQMRGVKQKSEYRQMIENNL
>NZ_CP051167.1|WP_168568010.1|1017376_1018258_-|ABC-transporter-permease
MALLKKGLPDALQATQRPTLSMQLMWVGLSITLIFIAIALFAPLLQDWGWIDDPREFLANPVHEPPSADYWFGTSRLGYDVFSRTLFGTQVAWKIVLLATALSMAIGVPLGLVSGYLGGKLDRVLLFVMDTIYTLPGLLLSITLAFVVGRGILNAAIALSIAYVPQYYRVVRNHTVSVKTELFVEAAQAIGAPTSRVLSRYLFLNVIQSVPVLFTLNAADAILVLGGLGFLGLGLPEEIPEWGHDLRQALDALSTGVWWTAFFPGCTMTLMVVGLSLLGEGLNELVNPKFRRE
>NZ_CP051167.1|WP_168568009.1|1016356_1017244_-|ROK-family-protein
MDQVIGVDLGGSAIKLGRFDREGECLESLTIETPQPAQPDAVLQAIARAVETIDRDRAAVAIGLGTPGPVDGTGRIAKVAINLDGWQDVAVADYLEAKTGKPTILANDANCAGLGEAWLGAGKRFRNSIMLTLGTGVGGAIILDGELFVGHTGAAGELGLITLNLYGHECHSGNNGSLEQHVSVQAIRRNTGVSPAELGHMAQAGNREALAFWETYGHQLGAGLASLIYVLTPEAIIIGGGISASAEFFLPHAKAEVERRVIAACRPHLEILVAELGNSAGMVGAAKLAWGLAKI
>NZ_CP051167.1|WP_168568019.1|1032607_1033582_-|WYL-domain-containing-protein
MGQKCTHITDALYILRKLTERPYPREELIVVLGEFLEQTDRKPGDVAQKLHRIVRELRDLGFAIDCAPHRPYTLVESNFPLILSATQRQSLYLAVQFLEDMGFATQAQQIAALVNLDATDAPPDIQVDFSPPTDYSNPDYEKILHALQDRCAQQYRYRIHYCNSQKQNLRLDLDRSEIRLHDGALYLFAFVPDWKPKPRGGRVHNVENNGLFRIDRIKSVGAPSTVGWVFSEFPTLKIRYRMSGPLATYKPRRVQERVVKRDLVRRYVEIETVEDYLFWFRQRIFRYGANARVLDPPWLAAEIGEELRRAAAQYQAGDSRENSS
>NZ_CP051167.1|WP_168568020.1|1033800_1035924_+|type-I-D-CRISPR-associated-helicase-Cas3'
MKLRLHGLHSQLNPGVGRCPLGCDRHCQVRERAPGLQPPPGATCPLSSHQAQTFAAVRFGDADLIFNKSATGDGKTLGGTLPTLLDPQFRLMALYPTIELVEDQTRQQQRYHELFGLQSRDRVDRLYGEELSRRVRERDSNKFQELLDAIYHTPILLTNPDIFHYITHYRYRQAAFDRALLPLALAEWPDLWMFDEFHIFGPHQEAAALNSLTLIRRSQQQRRPRRFLFTSATPKPDFIAQLARAEFKIAEIEGIYANETTPGFRQILQPVELEFVQLGDGDAVQWLVESADRLDRWLRGDRAGRGLIVLNAISSVNRAIAQLTERLPGVTVCEISGRIDRRERGRIQAQLQASPDPVLVVATSAVDVGVDFRINLLVFESSDAATVVQRLGRLGRHPGFSHYRAAILIPKQMPWVMPRLGEWGDRQEPVGRPELQEAIAIAFDPPKSFAEYRQKWGPLQAHGMLAEISRESNKVSEILRDRMREDLGRVYGDRFDRYRKCWFALGKNPVGKATQKELLRFRGATAIQAAIADGSRIYTYDLLRLLPYTWIERCDRETFLEAARTADCSPDAFDDRYIHVYLKVREWLDNRQSLSLQTQRDTDELKTCELTLLDRLAIVGHPQPEVSTCLQRRKLLAFLVPVHRSQPSSHWQVSYTLQLGPHFGLYRLTDAGGNAYACAFDRDALLLDALKFKLRRFCRTQPQSLIF
>NZ_CP051167.1|WP_168568021.1|1035934_1038868_+|type-I-D-CRISPR-associated-protein-Cas10d/Csc3
MQTLMQQLLLTSLDPETDPILCEYIDIILPAVEREFGSMTALGGDRDRHYNILCTLKDPLAAEKARNWSDRPDQNLCVHVLNALLLGWNLAEHHLPTSLSDEEKRLFCLGITLHDYNKYCHGQGEEAPKASEIDDILALCREIGARLNFSAFWPQWETYLSDIGFLAQNTQFKCGTNTYPSNWPEFAIADSRRLTHPLRHLLGWSDIAVHLNDPADIATETAGERLQEHLNLLGIRKTLVYHRLRDSLGILTNGIHNATLHYARELGWEAIVFFARGVVYLAPKNFSSPDLADLKQFIWEQIALILGNKMLDGDVGFRRDGKGLKVAPQTSELFPPAQLIRQLSDVIAARVNNAKNPATPKRLAKLVERGLITEDREKELLKGADLRSDRLAEFIIVIQREFLGNCEDYGPWMLEALDLATIFNPEDLQINIGGVNYGWYLAAAQYFSKNSTLDLEQTTELLAEIGDRLADWATENNSLPAYSSPTQEVFDRYLQYYLDFSGIKTELPPFGQELNAYAIAKTRKAKQPICSLSSGEFPSEDQLDSVVLFKPQQYSNKNTLGGSKIKRGISKIWSLEMLLRQALWSARAGKLEEQQPVFLYIFPAYVYAPQMIKAIRVLVEELKTVNLWEIRKYWLNHELEVSQLSHWLWLREDAEIGRFAKGSYDSKDLPFMATVYTTTLGETVTEAWVHPAFLATILPKLLGVRVVATASNVPLYRSDREFCGSAVLDGVAGFWSLLHCPSEVRTEQLDSVLTRLLVVYTLHLDNRAHQSDARWGALNRTVREVMTDVLNIFAIAREGLRRRQHDPSPEEVERYWNFARIWSDLDKTMQEKLNFITELVRQYRTFYQVKVTDSSHAILLPFSKVLETILSVPTQVNEEDLILQGAGLLKDAIDRQNIYTRPLMMDKSVDFATRQQQELEAIHRFVQTCVCDLFGTLYRGDRALLQENRNRLKSGAEFAYRWLALQEKNERDLASPS
>NZ_CP051167.1|WP_168568022.1|1038930_1039929_+|type-I-D-CRISPR-associated-protein-Cas7/Csc2
MTQLNALKNEFANDFPRLASGHYVHFILLRHSQSFPVFQTDGVLNTARTQAGINTTDTISRLVLFKRKQTTPERLAGRELLRSVSLISGDPDAENYCQYNGEKSCKQCPDCIIYGFAIGDSGSERSKVYSDSAFSLSSYEQSHRSFIFNGPSEAGTMSEGGQMRNAINELDHVLPEVTFPTVETLRDPTYEGFLYVLGNLLRTRRYGAQETRTGTMRNYPIAILLTDGEIFSNLYFTQALYDELKGDLNAPIADLKTVANTVVNRLLEDEPIRISHKLMGNDLEQFLDEVSEIYKDEEQLTEMLANLYEQTETYCNHYGAKSSKRSGKSGKK
>NZ_CP051167.1|WP_168568023.1|1040007_1040784_+|type-I-D-CRISPR-associated-protein-Cas5/Csc1
MVLYYCQLTLHDNVFFATREMGILYETEQYLHNWALSYAFFGDTYIPLSYANLGQYIQKPGYLDPKFEQNLLYLNPQGIYVFPGFPQRYFYQINTFKAAQVNYYGRSKKFGEKGASRNYPINYGRAKELGVGSEYSTYIYSKKEIDLPRWIRLGKWMAKVKVDSHQIPDSAIALRSGTYACHHPLNPLDLPESQEILLYNRIVMPPVSLIAQAQLSGEYCELKGDDWDRFRRDFPELKAEVCLPVGVAYGAREIANVS
>NZ_CP051167.1|WP_168568024.1|1040773_1041622_+|CRISPR-system-precrRNA-processing-endoribonuclease-RAMP-protein-Cas6
MSVNLPAHSDSLYSIVVELRAIDSGQPPATLGRALHAQVLRWIELGNPEVSASIHDRQSSPLSVSGLIGNRRPTQTESGDYFIVRICILDGDIVQPLLRGLSEWGTEPLILAKFPFLMTRTYMFADSHPLASSSSYSALANIKESDSSIELNFTSPTSFKQKQDIQTFPLTELVFGSLQRRWNMFAPPELQFPKIEWEGVVSAYELRTHALRLEGGAEIGTQGWIRYRFRDSEQARMATILGQYAFFAGVGRKTTMGMGQTRVMEKKKAKGKPKRKFKKPYK
>NZ_CP051167.1|WP_168571731.1|1042133_1042715_+|CRISPR-associated-protein-Cas4
MMDDYLPLSYLNAWEYCPRRFYWEYVLGEMEENEHILMGTHLHRNIDRENVSREGNLLIHRQQWVWSDRLQVKGIVDAVEECETIRVPLEYKKGRMARHLNDHFQLCAAALCLEERLNCSIEYGEIFYHGNRRRERVEFTLQLRMATEEAIAAARQAVNELMPPPLKRLAKCRDCSLFNICLPKEVKKLHEFE
>NZ_CP051167.1|WP_168568025.1|1042741_1043719_+|type-I-D-CRISPR-associated-endonuclease-Cas1
MSVLYVTQPNAVLSKKYEAFKLAIAAEDGSVNKQSIPAQTLEQIVLMGNPSITGEALCYALELGLPIHYLSIFGKYLGSALPGYSRNGQLRLAQYAAHEDPSQRLTLVKAIVAGKIYNQYNVLYRHGEKDNPLKQRRGAIAQQETLDQTRGMEGLAAREYFARWEAMLPGPWTFPGRHRRPPTDPVNALLSFSYGLLRVQVTAAVHLAGLDPYIGYLHETTRGQPAMVLDLMEEFRPLVADNVVLSVLAHKEIKPDDFTESLGAYRLADGARKAFLQAFERKLNAEFQHPVFDYRCTYRRAIELQARLLARHLQEGVPYKPLVVR
>NZ_CP051167.1|WP_168568026.1|1043715_1044009_+|CRISPR-associated-endonuclease-Cas2
MKDLLYLIVYDLPATAAGNKRRQRLHDLLCGYGTWKQYSLFECFLDAKQFASLQIKIETLIKPAEDAVCIYVLDAMAVRKTIVYGMPPPRQETVTIV
>NZ_CP051167.1|WP_168568027.1|1049764_1050976_-|amidohydrolase
MLSTPLDRHCADESRLRPEIHNLQMTLVEWRRHLHQHPELGFKEVQTAEFVSKKLQEWGVEHQTGIAKTGIVATIRGSKPGPVLAIRADMDALPIQEENEVSYRSRHDGIMHACGHDGHTAIALGTVYYLSRHRDDFAGTVKFIFQPAEEGPGGAQPMIEAGVLENPRPDAIVGLHLWNNLPLGTVGVRSGPLMAAVELFRCTIFGKGGHGAMPHQTVDAIVVGSQVVQALQTIVARNVDPIESAVVTVGEFHAGSANNVIAGKAQLSGTVRYFNPKMEDLIRHRFAEIIAGVCHSHGARYDLDYWQLYPSVVNDRAIADLVRSVAEHVVETPAGIVPKCQTMGGEDMSFFLQEVPGCYFFLGSANESKDLAYPHHHPRFDFDETALGMGVEMFVRCVEKFCS

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Crispr_ID: NZ_CP051167_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_5

1044218-1049480

TypeV,TypeI-D

N:A

Consensus_repeat	Method
CTTTCAATTCAATGAATCCCGGCAACGGG---------ATTGAAAC	PILER-CR
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CRISPRCasFinder
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CRT
CTTTCAATTCAATGAATCCCGGCAACGGG---------ATTGAAAC	PILER-CR
CTTTCAATTCAATGAATCCCGGCAACGGG---------ATTGAAAC	PILER-CR

71 spacers

cas2,cas1,cas4,cas6,csc1gr5,csc2gr7,cas10d,cas3,WYL,cas14j

The CRISPR arrays of NZ_CP051167_5

>merge|NZ_CP051167|5|1044218-1049480|PILER-CR,CRISPRCasFinder,CRT,PILER-CR,PILER-CR
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTAGGCGCTTCGTTGCAAGGTACTAGTGTCTCCGGACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACATTAAATAAAACTCCTATTGAAAATTTATTAGGAACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCTACTCACAAAAAAGAATTGAATAAAAGGAAGAACTACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACAACGCACCCTATCTCACTAAGTTGGTGTGGGATATCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCCAGGGAAGCCGAAGCGATCGCCGACAGATTGACGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCGTGACACTTTCGATGAATTCAATTAATTCTTGTTTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACAGTAAGGCGTCGAAGAACCCATCATACTCTTCATCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTCACGGCCTGCAAGAATTTTATCGGGGAGTTACAGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACAAACAACTCCTCGAACAGGACATACTCATGCGCAAGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACAAGCGGATGATAAAATAATTACCTCTTCCAGCAATTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGCAAAAAGCAATGGGACTATTAAAGCTTCTGGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTCGCATCTTCGTAGCGCAATCGAGTATGTGAGACGAGCACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTTTTGTATGCTTTTTTGTATACTTTTTTGTCGAGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTTCCCTTGTCCCCCTCTAAATTTTCTCGGATGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTGCAGCCGCCCTGTTTTGGAGTGTTTATGCTTAAGTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCCTCGATCGCCTGAATCGTTTTTCCTAGACCCATATCGTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTAATATAACAGAATTTGATATCAACTCGCCTTTACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACATCGCGGAACAGATAAGCCAGAACGCTCCTTGGCCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCCCTCGAGATCGACATTGCAGAGAGTGGCACTCTCGACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCTTTCCAGTAATCTGGCCTGTAAGTCTCGTCTACAACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTGTCGAGAATTACGTAGGAAGTGAGAAGGACAAGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTTCTTGTACGGCAATCCGCCGCGCATCATCTAAAGGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTGTCTAACTTAGAGTTAGAAAGGCGGGGTAATTTCCTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGAAACGAATCGCCTTCGTCTCAATACCGCGATGTACCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACAGCTCAATTTGCAGTTGGCGTGATCGCCCCTCCAGACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCGCTATTATGGCTAAAATTTCTTCTTCGGAGAACGATAAGGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTTCTTTGAAGTATCCCATGGTATTTGGTCTCCGTTTCCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGCGCCTATCCGCATCCTGACGGAGGGACTTCCGGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTAACCAAAGGAAGTCCGCCTTTAGATCGATAAAGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGAGGCGCGACTCTGTCATTCCCTCCCCGAAGGAGAGAATGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACATGGGAAGCTCGCCATTGCTTAAGTGGCTTCCTTTAAGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACACCTCTTCAGGTTTAAGTTTTGTCGAATAGATCCAGCTCTTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACAACCTCAGTGGCGCATCCCTAGCCGATGCAATCCTTTACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACACTCGACCAGGGAATCGGGAACCGATACCCCATCTAGACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGACCGTCTCGCACTTCGAGACGAGCATTGTTTTGTACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCAAGTCCCTCGAAGAGGTAGCGGGCGAGATGAGATACCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGAGTATTCACGCGCTTTAAGCGCGTAGTGGTCCCCTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACAGGTACTAAAAGAGATACCATCGGGGTAGGCGAGAATCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACAGCAAATTGGGGAGGTAGAAAAGGAAGGAACTAAACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGATATAGACAATAAGTTTCTGAATCGCCACCACCACCTTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACAAAGATGAACAGCTCAAATTCACTTCACTCAAGTTCGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCGTACTCCTTATACAACCCCAAAAGCTTAGCGCCCATTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCGATCTTCCATTTATTGGAGCAGGAGGGGCGTCCCGTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACAAATAGTTCCTCGAATAGAGCATACTTATGCGCGAGGAAGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGAGGCGCGCAACCAAACCCTAGACGCCGAAAGGGAAATATCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTTGAATCATCTTATTCGTATCCTCCGCCGATCGCACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTTTTCGCCTCGATTTCCTTGTCGATCAGGTCTAGATTTTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGGCAAGAAATAGTGAGGGTAGGGATTTCGTGAGAGAGGGTTTCCGACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGGATTGAACTAGATATCTTAATCCACAGGTATATCCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTAGAGACCCAACAAGGAGGTATTACAGGTAAAGGTTTAATCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACAATGAATTAAAGTTCGACGAGACGATCTCGGCGAGACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACACGGCATACTTCGCCGATCCTATCGAGCCATCGTCCCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGGCTTCGTATGCCTGCTGCATTTCCACAGGACGATCATCTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACATATTCCGCTTCAAGCGTTCCCGTCATCGATTCCAACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCGCACAGGAGCCAATGCGTCGCATCGCCGTCGTCGCCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGAAACTTCCGTTGCCGTAGCGCTGGCTGGAGGTTTCCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTTCGTCTTGGAACGCCGAGGCAAACCCCATTGAGTAACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACAGAACCCCAGCAACCCAGTAGCCTCCCTCCCTGCTTTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGTCAACCGATAATTTGAGGCCAGGAAACACCTTGGCGGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCGTATCCTCCGCCCCCTTCGTCCCCTTCCCCTTGTGGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCGTTGGGCTTTCCCCGAACCTGCCGGGGTTGGATTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCGAAAATCGACCCCATTATGAAACCTAGTTTCCCCTAAGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCTTCTCCAACTGCATCATTTGAGCAGGAGAGAAGTTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTAGCTCTGCTTAATCAGCAATAGGGTTCACATTACCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTTGATACGTTCTTGAACGAAAGAACCTTCGTATGCCAGGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACAGTCTCACTTTTTGCCCCAGCAGTTCGGCCTTCGTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACACCCGACTGGAAAGCTAGAGTCTGCCGATCTTTTTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAGCATAGGGGTCATTCAAAACGGCGGCAGCTTTTTCCACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACATCGAACTGACCCGCTTGAATGAGGCGATCGCACTCGGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACAAAAAACTTATTCAGTGGACACAAGCGAATTACGATGTACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGCGGGTGGCTAGCGAGTGGTTGCCGCGTGCCTCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAT

>NZ_CP051167|5|4|1044218-1045628|PILER-CR
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAGGCGCTTCGTTGCAAGGTACTAGTGTCTCCGGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATTAAATAAAACTCCTATTGAAAATTTATTAGGAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CTACTCACAAAAAAGAATTGAATAAAAGGAAGAACTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AACGCACCCTATCTCACTAAGTTGGTGTGGGATAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCAGGGAAGCCGAAGCGATCGCCGACAGATTGACG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTGACACTTTCGATGAATTCAATTAATTCTTGTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGTAAGGCGTCGAAGAACCCATCATACTCTTCAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TCACGGCCTGCAAGAATTTTATCGGGGAGTTACAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAACAACTCCTCGAACAGGACATACTCATGCGCAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAGCGGATGATAAAATAATTACCTCTTCCAGCAATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GCAAAAAGCAATGGGACTATTAAAGCTTCTGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TCGCATCTTCGTAGCGCAATCGAGTATGTGAGACGAGCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTTTGTATGCTTTTTTGTATACTTTTTTGTCGAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCCCTTGTCCCCCTCTAAATTTTCTCGGATG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TGCAGCCGCCCTGTTTTGGAGTGTTTATGCTTAAGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCTCGATCGCCTGAATCGTTTTTCCTAGACCCATATCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAATATAACAGAATTTGATATCAACTCGCCTTTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATCGCGGAACAGATAAGCCAGAACGCTCCTTGGC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCCTCGAGATCGACATTGCAGAGAGTGGCACTCTCGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCTTTCCAGTAATCTGGCCTGTAAGTCTCGTCTACAACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTGTCGAGAATTACGTAGGAAGTGAGAAGGACAAGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCTTGTACGGCAATCCGCCGCGCATCATCTAAAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TGTCTAACTTAGAGTTAGAAAGGCGGGGTAATTTCCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAAACGAATCGCCTTCGTCTCAATACCGCGATGTAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGCTCAATTTGCAGTTGGCGTGATCGCCCCTCCAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGCTATTATGGCTAAAATTTCTTCTTCGGAGAACGATAAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCTTTGAAGTATCCCATGGTATTTGGTCTCCGTTTC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGCGCCTATCCGCATCCTGACGGAGGGACTTCCGGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTAACCAAAGGAAGTCCGCCTTTAGATCGATAAAGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGGCGCGACTCTGTCATTCCCTCCCCGAAGGAGAGAATG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATGGGAAGCTCGCCATTGCTTAAGTGGCTTCCTTTAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACCTCTTCAGGTTTAAGTTTTGTCGAATAGATCCAGCTCTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AACCTCAGTGGCGCATCCCTAGCCGATGCAATCCTTTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACTCGACCAGGGAATCGGGAACCGATACCCCATCTAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GACCGTCTCGCACTTCGAGACGAGCATTGTTTTGTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CAAGTCCCTCGAAGAGGTAGCGGGCGAGATGAGATAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGTATTCACGCGCTTTAAGCGCGTAGTGGTCCCCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGGTACTAAAAGAGATACCATCGGGGTAGGCGAGAAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGCAAATTGGGGAGGTAGAAAAGGAAGGAACTAAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GATATAGACAATAAGTTTCTGAATCGCCACCACCACC
TTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAAGATGAACAGCTCAAATTCACTTCACTCAAGTTCG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTACTCCTTATACAACCCCAAAAGCTTAGCGCCCATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGATCTTCCATTTATTGGAGCAGGAGGGGCGTCCCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAATAGTTCCTCGAATAGAGCATACTTATGCGCGAGGAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGGCGCGCAACCAAACCCTAGACGCCGAAAGGGAAATAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTGAATCATCTTATTCGTATCCTCCGCCGATCGCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTTTCGCCTCGATTTCCTTGTCGATCAGGTCTAGATTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGCAAGAAATAGTGAGGGTAGGGATTTCGTGAGAGAGGGTTTCCGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGATTGAACTAGATATCTTAATCCACAGGTATATC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAGAGACCCAACAAGGAGGTATTACAGGTAAAGGTTTAAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AATGAATTAAAGTTCGACGAGACGATCTCGGCGAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACGGCATACTTCGCCGATCCTATCGAGCCATCGTCC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGCTTCGTATGCCTGCTGCATTTCCACAGGACGATCATCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATATTCCGCTTCAAGCGTTCCCGTCATCGATTCCAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGCACAGGAGCCAATGCGTCGCATCGCCGTCGTCGC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAAACTTCCGTTGCCGTAGCGCTGGCTGGAGGTTTC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCGTCTTGGAACGCCGAGGCAAACCCCATTGAGTAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGAACCCCAGCAACCCAGTAGCCTCCCTCCCTGCTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GTCAACCGATAATTTGAGGCCAGGAAACACCTTGGCGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTATCCTCCGCCCCCTTCGTCCCCTTCCCCTTGTGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTTGGGCTTTCCCCGAACCTGCCGGGGTTGGATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGAAAATCGACCCCATTATGAAACCTAGTTTCCCCTAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CTTCTCCAACTGCATCATTTGAGCAGGAGAGAAGTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAGCTCTGCTTAATCAGCAATAGGGTTCACATTAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTGATACGTTCTTGAACGAAAGAACCTTCGTATGCCAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGTCTCACTTTTTGCCCCAGCAGTTCGGCCTTCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACCCGACTGGAAAGCTAGAGTCTGCCGATCTTTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAGC	ATAGGGGTCATTCAAAACGGCGGCAGCTTTTTCCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATCGAACTGACCCGCTTGAATGAGGCGATCGCACTCGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAAAAACTTATTCAGTGGACACAAGCGAATTACGATGTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GCGGGTGGCTAGCGAGTGGTTGCCGCGTGCCT


>NZ_CP051167|5|4|1044218-1049480|CRISPRCasFinder
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAGGCGCTTCGTTGCAAGGTACTAGTGTCTCCGGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATTAAATAAAACTCCTATTGAAAATTTATTAGGAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CTACTCACAAAAAAGAATTGAATAAAAGGAAGAACTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AACGCACCCTATCTCACTAAGTTGGTGTGGGATAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCAGGGAAGCCGAAGCGATCGCCGACAGATTGACG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTGACACTTTCGATGAATTCAATTAATTCTTGTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGTAAGGCGTCGAAGAACCCATCATACTCTTCAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TCACGGCCTGCAAGAATTTTATCGGGGAGTTACAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAACAACTCCTCGAACAGGACATACTCATGCGCAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAGCGGATGATAAAATAATTACCTCTTCCAGCAATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GCAAAAAGCAATGGGACTATTAAAGCTTCTGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TCGCATCTTCGTAGCGCAATCGAGTATGTGAGACGAGCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTTTGTATGCTTTTTTGTATACTTTTTTGTCGAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCCCTTGTCCCCCTCTAAATTTTCTCGGATG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TGCAGCCGCCCTGTTTTGGAGTGTTTATGCTTAAGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCTCGATCGCCTGAATCGTTTTTCCTAGACCCATATCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAATATAACAGAATTTGATATCAACTCGCCTTTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATCGCGGAACAGATAAGCCAGAACGCTCCTTGGC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCCTCGAGATCGACATTGCAGAGAGTGGCACTCTCGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CTTTCCAGTAATCTGGCCTGTAAGTCTCGTCTACAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TGTCGAGAATTACGTAGGAAGTGAGAAGGACAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCTTGTACGGCAATCCGCCGCGCATCATCTAAAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TGTCTAACTTAGAGTTAGAAAGGCGGGGTAATTTCCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAAACGAATCGCCTTCGTCTCAATACCGCGATGTAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGCTCAATTTGCAGTTGGCGTGATCGCCCCTCCAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGCTATTATGGCTAAAATTTCTTCTTCGGAGAACGATAAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCTTTGAAGTATCCCATGGTATTTGGTCTCCGTTTC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GCGCCTATCCGCATCCTGACGGAGGGACTTCCGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAACCAAAGGAAGTCCGCCTTTAGATCGATAAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGGCGCGACTCTGTCATTCCCTCCCCGAAGGAGAGAATG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATGGGAAGCTCGCCATTGCTTAAGTGGCTTCCTTTAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACCTCTTCAGGTTTAAGTTTTGTCGAATAGATCCAGCTCTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AACCTCAGTGGCGCATCCCTAGCCGATGCAATCCTTTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACTCGACCAGGGAATCGGGAACCGATACCCCATCTAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GACCGTCTCGCACTTCGAGACGAGCATTGTTTTGTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CAAGTCCCTCGAAGAGGTAGCGGGCGAGATGAGATAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGTATTCACGCGCTTTAAGCGCGTAGTGGTCCCCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGGTACTAAAAGAGATACCATCGGGGTAGGCGAGAAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGCAAATTGGGGAGGTAGAAAAGGAAGGAACTAAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GATATAGACAATAAGTTTCTGAATCGCCACCACCACC
TTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAAGATGAACAGCTCAAATTCACTTCACTCAAGTTCG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTACTCCTTATACAACCCCAAAAGCTTAGCGCCCATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGATCTTCCATTTATTGGAGCAGGAGGGGCGTCCCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAATAGTTCCTCGAATAGAGCATACTTATGCGCGAGGAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGGCGCGCAACCAAACCCTAGACGCCGAAAGGGAAATAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTGAATCATCTTATTCGTATCCTCCGCCGATCGCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTTTCGCCTCGATTTCCTTGTCGATCAGGTCTAGATTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGCAAGAAATAGTGAGGGTAGGGATTTCGTGAGAGAGGGTTTCCGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGATTGAACTAGATATCTTAATCCACAGGTATATC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAGAGACCCAACAAGGAGGTATTACAGGTAAAGGTTTAAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AATGAATTAAAGTTCGACGAGACGATCTCGGCGAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACGGCATACTTCGCCGATCCTATCGAGCCATCGTCC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGCTTCGTATGCCTGCTGCATTTCCACAGGACGATCATCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATATTCCGCTTCAAGCGTTCCCGTCATCGATTCCAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGCACAGGAGCCAATGCGTCGCATCGCCGTCGTCGC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAAACTTCCGTTGCCGTAGCGCTGGCTGGAGGTTTC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCGTCTTGGAACGCCGAGGCAAACCCCATTGAGTAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGAACCCCAGCAACCCAGTAGCCTCCCTCCCTGCTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GTCAACCGATAATTTGAGGCCAGGAAACACCTTGGCGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTATCCTCCGCCCCCTTCGTCCCCTTCCCCTTGTGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTTGGGCTTTCCCCGAACCTGCCGGGGTTGGATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGAAAATCGACCCCATTATGAAACCTAGTTTCCCCTAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CTTCTCCAACTGCATCATTTGAGCAGGAGAGAAGTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAGCTCTGCTTAATCAGCAATAGGGTTCACATTAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTGATACGTTCTTGAACGAAAGAACCTTCGTATGCCAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGTCTCACTTTTTGCCCCAGCAGTTCGGCCTTCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACCCGACTGGAAAGCTAGAGTCTGCCGATCTTTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAGC	ATAGGGGTCATTCAAAACGGCGGCAGCTTTTTCCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATCGAACTGACCCGCTTGAATGAGGCGATCGCACTCGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAAAAACTTATTCAGTGGACACAAGCGAATTACGATGTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GCGGGTGGCTAGCGAGTGGTTGCCGCGTGCCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAT

>NZ_CP051167|5|2|1044218-1049480|CRT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAGGCGCTTCGTTGCAAGGTACTAGTGTCTCCGGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATTAAATAAAACTCCTATTGAAAATTTATTAGGAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CTACTCACAAAAAAGAATTGAATAAAAGGAAGAACTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AACGCACCCTATCTCACTAAGTTGGTGTGGGATAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCAGGGAAGCCGAAGCGATCGCCGACAGATTGACG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTGACACTTTCGATGAATTCAATTAATTCTTGTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGTAAGGCGTCGAAGAACCCATCATACTCTTCAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TCACGGCCTGCAAGAATTTTATCGGGGAGTTACAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAACAACTCCTCGAACAGGACATACTCATGCGCAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAGCGGATGATAAAATAATTACCTCTTCCAGCAATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GCAAAAAGCAATGGGACTATTAAAGCTTCTGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TCGCATCTTCGTAGCGCAATCGAGTATGTGAGACGAGCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTTTGTATGCTTTTTTGTATACTTTTTTGTCGAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCCCTTGTCCCCCTCTAAATTTTCTCGGATG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TGCAGCCGCCCTGTTTTGGAGTGTTTATGCTTAAGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCTCGATCGCCTGAATCGTTTTTCCTAGACCCATATCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAATATAACAGAATTTGATATCAACTCGCCTTTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATCGCGGAACAGATAAGCCAGAACGCTCCTTGGC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCCTCGAGATCGACATTGCAGAGAGTGGCACTCTCGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CTTTCCAGTAATCTGGCCTGTAAGTCTCGTCTACAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TGTCGAGAATTACGTAGGAAGTGAGAAGGACAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCTTGTACGGCAATCCGCCGCGCATCATCTAAAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TGTCTAACTTAGAGTTAGAAAGGCGGGGTAATTTCCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAAACGAATCGCCTTCGTCTCAATACCGCGATGTAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGCTCAATTTGCAGTTGGCGTGATCGCCCCTCCAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGCTATTATGGCTAAAATTTCTTCTTCGGAGAACGATAAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCTTTGAAGTATCCCATGGTATTTGGTCTCCGTTTC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GCGCCTATCCGCATCCTGACGGAGGGACTTCCGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAACCAAAGGAAGTCCGCCTTTAGATCGATAAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGGCGCGACTCTGTCATTCCCTCCCCGAAGGAGAGAATG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATGGGAAGCTCGCCATTGCTTAAGTGGCTTCCTTTAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACCTCTTCAGGTTTAAGTTTTGTCGAATAGATCCAGCTCTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AACCTCAGTGGCGCATCCCTAGCCGATGCAATCCTTTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACTCGACCAGGGAATCGGGAACCGATACCCCATCTAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GACCGTCTCGCACTTCGAGACGAGCATTGTTTTGTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CAAGTCCCTCGAAGAGGTAGCGGGCGAGATGAGATAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGTATTCACGCGCTTTAAGCGCGTAGTGGTCCCCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGGTACTAAAAGAGATACCATCGGGGTAGGCGAGAAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGCAAATTGGGGAGGTAGAAAAGGAAGGAACTAAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GATATAGACAATAAGTTTCTGAATCGCCACCACCACC
TTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAAGATGAACAGCTCAAATTCACTTCACTCAAGTTCG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTACTCCTTATACAACCCCAAAAGCTTAGCGCCCATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGATCTTCCATTTATTGGAGCAGGAGGGGCGTCCCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAATAGTTCCTCGAATAGAGCATACTTATGCGCGAGGAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGGCGCGCAACCAAACCCTAGACGCCGAAAGGGAAATAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTGAATCATCTTATTCGTATCCTCCGCCGATCGCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTTTCGCCTCGATTTCCTTGTCGATCAGGTCTAGATTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGCAAGAAATAGTGAGGGTAGGGATTTCGTGAGAGAGGGTTTCCGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGATTGAACTAGATATCTTAATCCACAGGTATATC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAGAGACCCAACAAGGAGGTATTACAGGTAAAGGTTTAAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AATGAATTAAAGTTCGACGAGACGATCTCGGCGAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACGGCATACTTCGCCGATCCTATCGAGCCATCGTCC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGCTTCGTATGCCTGCTGCATTTCCACAGGACGATCATCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATATTCCGCTTCAAGCGTTCCCGTCATCGATTCCAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGCACAGGAGCCAATGCGTCGCATCGCCGTCGTCGC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAAACTTCCGTTGCCGTAGCGCTGGCTGGAGGTTTC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCGTCTTGGAACGCCGAGGCAAACCCCATTGAGTAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGAACCCCAGCAACCCAGTAGCCTCCCTCCCTGCTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GTCAACCGATAATTTGAGGCCAGGAAACACCTTGGCGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTATCCTCCGCCCCCTTCGTCCCCTTCCCCTTGTGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTTGGGCTTTCCCCGAACCTGCCGGGGTTGGATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGAAAATCGACCCCATTATGAAACCTAGTTTCCCCTAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CTTCTCCAACTGCATCATTTGAGCAGGAGAGAAGTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAGCTCTGCTTAATCAGCAATAGGGTTCACATTAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTGATACGTTCTTGAACGAAAGAACCTTCGTATGCCAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGTCTCACTTTTTGCCCCAGCAGTTCGGCCTTCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACCCGACTGGAAAGCTAGAGTCTGCCGATCTTTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAGC	ATAGGGGTCATTCAAAACGGCGGCAGCTTTTTCCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATCGAACTGACCCGCTTGAATGAGGCGATCGCACTCGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAAAAACTTATTCAGTGGACACAAGCGAATTACGATGTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GCGGGTGGCTAGCGAGTGGTTGCCGCGTGCCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAT

>NZ_CP051167|5|5|1045736-1046217|PILER-CR
	TAGGCGCTTCGTTGCAAGGTACTAGTGTCTCCGGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATTAAATAAAACTCCTATTGAAAATTTATTAGGAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CTACTCACAAAAAAGAATTGAATAAAAGGAAGAACTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AACGCACCCTATCTCACTAAGTTGGTGTGGGATAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCAGGGAAGCCGAAGCGATCGCCGACAGATTGACG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTGACACTTTCGATGAATTCAATTAATTCTTGTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGTAAGGCGTCGAAGAACCCATCATACTCTTCAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TCACGGCCTGCAAGAATTTTATCGGGGAGTTACAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAACAACTCCTCGAACAGGACATACTCATGCGCAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAGCGGATGATAAAATAATTACCTCTTCCAGCAATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GCAAAAAGCAATGGGACTATTAAAGCTTCTGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TCGCATCTTCGTAGCGCAATCGAGTATGTGAGACGAGCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTTTGTATGCTTTTTTGTATACTTTTTTGTCGAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCCCTTGTCCCCCTCTAAATTTTCTCGGATG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TGCAGCCGCCCTGTTTTGGAGTGTTTATGCTTAAGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCTCGATCGCCTGAATCGTTTTTCCTAGACCCATATCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAATATAACAGAATTTGATATCAACTCGCCTTTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATCGCGGAACAGATAAGCCAGAACGCTCCTTGGC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCCTCGAGATCGACATTGCAGAGAGTGGCACTCTCGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCTTTCCAGTAATCTGGCCTGTAAGTCTCGTCTACAACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTGTCGAGAATTACGTAGGAAGTGAGAAGGACAAGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCTTGTACGGCAATCCGCCGCGCATCATCTAAAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TGTCTAACTTAGAGTTAGAAAGGCGGGGTAATTTCCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAAACGAATCGCCTTCGTCTCAATACCGCGATGTAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGCTCAATTTGCAGTTGGCGTGATCGCCCCTCCAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGCTATTATGGCTAAAATTTCTTCTTCGGAGAACGATAAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCTTTGAAGTATCCCATGGTATTTGGTCTCCGTTTC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGCGCCTATCCGCATCCTGACGGAGGGACTTCCGGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTAACCAAAGGAAGTCCGCCTTTAGATCGATAAAGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGGCGCGACTCTGTCATTCCCTCCCCGAAGGAGAGAATG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATGGGAAGCTCGCCATTGCTTAAGTGGCTTCCTTTAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACCTCTTCAGGTTTAAGTTTTGTCGAATAGATCCAGCTCTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AACCTCAGTGGCGCATCCCTAGCCGATGCAATCCTTTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACTCGACCAGGGAATCGGGAACCGATACCCCATCTAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GACCGTCTCGCACTTCGAGACGAGCATTGTTTTGTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CAAGTCCCTCGAAGAGGTAGCGGGCGAGATGAGATAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGTATTCACGCGCTTTAAGCGCGTAGTGGTCCCCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGGTACTAAAAGAGATACCATCGGGGTAGGCGAGAAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGCAAATTGGGGAGGTAGAAAAGGAAGGAACTAAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GATATAGACAATAAGTTTCTGAATCGCCACCACCACC
TTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAAGATGAACAGCTCAAATTCACTTCACTCAAGTTCG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTACTCCTTATACAACCCCAAAAGCTTAGCGCCCATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGATCTTCCATTTATTGGAGCAGGAGGGGCGTCCCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAATAGTTCCTCGAATAGAGCATACTTATGCGCGAGGAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGGCGCGCAACCAAACCCTAGACGCCGAAAGGGAAATAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTGAATCATCTTATTCGTATCCTCCGCCGATCGCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTTTCGCCTCGATTTCCTTGTCGATCAGGTCTAGATTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGCAAGAAATAGTGAGGGTAGGGATTTCGTGAGAGAGGGTTTCCGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGATTGAACTAGATATCTTAATCCACAGGTATATC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAGAGACCCAACAAGGAGGTATTACAGGTAAAGGTTTAAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AATGAATTAAAGTTCGACGAGACGATCTCGGCGAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACGGCATACTTCGCCGATCCTATCGAGCCATCGTCC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGCTTCGTATGCCTGCTGCATTTCCACAGGACGATCATCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATATTCCGCTTCAAGCGTTCCCGTCATCGATTCCAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGCACAGGAGCCAATGCGTCGCATCGCCGTCGTCGC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAAACTTCCGTTGCCGTAGCGCTGGCTGGAGGTTTC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCGTCTTGGAACGCCGAGGCAAACCCCATTGAGTAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGAACCCCAGCAACCCAGTAGCCTCCCTCCCTGCTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GTCAACCGATAATTTGAGGCCAGGAAACACCTTGGCGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTATCCTCCGCCCCCTTCGTCCCCTTCCCCTTGTGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTTGGGCTTTCCCCGAACCTGCCGGGGTTGGATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGAAAATCGACCCCATTATGAAACCTAGTTTCCCCTAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CTTCTCCAACTGCATCATTTGAGCAGGAGAGAAGTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAGCTCTGCTTAATCAGCAATAGGGTTCACATTAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTGATACGTTCTTGAACGAAAGAACCTTCGTATGCCAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGTCTCACTTTTTGCCCCAGCAGTTCGGCCTTCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACCCGACTGGAAAGCTAGAGTCTGCCGATCTTTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAGC	ATAGGGGTCATTCAAAACGGCGGCAGCTTTTTCCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATCGAACTGACCCGCTTGAATGAGGCGATCGCACTCGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAAAAACTTATTCAGTGGACACAAGCGAATTACGATGTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GCGGGTGGCTAGCGAGTGGTTGCCGCGTGCCT


>NZ_CP051167|5|6|1046323-1049480|PILER-CR
	TAGGCGCTTCGTTGCAAGGTACTAGTGTCTCCGGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATTAAATAAAACTCCTATTGAAAATTTATTAGGAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CTACTCACAAAAAAGAATTGAATAAAAGGAAGAACTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AACGCACCCTATCTCACTAAGTTGGTGTGGGATAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCAGGGAAGCCGAAGCGATCGCCGACAGATTGACG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTGACACTTTCGATGAATTCAATTAATTCTTGTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGTAAGGCGTCGAAGAACCCATCATACTCTTCAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TCACGGCCTGCAAGAATTTTATCGGGGAGTTACAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAACAACTCCTCGAACAGGACATACTCATGCGCAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAGCGGATGATAAAATAATTACCTCTTCCAGCAATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GCAAAAAGCAATGGGACTATTAAAGCTTCTGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TCGCATCTTCGTAGCGCAATCGAGTATGTGAGACGAGCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTTTGTATGCTTTTTTGTATACTTTTTTGTCGAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCCCTTGTCCCCCTCTAAATTTTCTCGGATG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TGCAGCCGCCCTGTTTTGGAGTGTTTATGCTTAAGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCTCGATCGCCTGAATCGTTTTTCCTAGACCCATATCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAATATAACAGAATTTGATATCAACTCGCCTTTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATCGCGGAACAGATAAGCCAGAACGCTCCTTGGC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CCCTCGAGATCGACATTGCAGAGAGTGGCACTCTCGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACCTTTCCAGTAATCTGGCCTGTAAGTCTCGTCTACAACTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTGTCGAGAATTACGTAGGAAGTGAGAAGGACAAGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCTTGTACGGCAATCCGCCGCGCATCATCTAAAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TGTCTAACTTAGAGTTAGAAAGGCGGGGTAATTTCCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAAACGAATCGCCTTCGTCTCAATACCGCGATGTAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGCTCAATTTGCAGTTGGCGTGATCGCCCCTCCAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGCTATTATGGCTAAAATTTCTTCTTCGGAGAACGATAAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCTTTGAAGTATCCCATGGTATTTGGTCTCCGTTTC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACGCGCCTATCCGCATCCTGACGGAGGGACTTCCGGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAACTAACCAAAGGAAGTCCGCCTTTAGATCGATAAAGCTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGGCGCGACTCTGTCATTCCCTCCCCGAAGGAGAGAATG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATGGGAAGCTCGCCATTGCTTAAGTGGCTTCCTTTAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACCTCTTCAGGTTTAAGTTTTGTCGAATAGATCCAGCTCTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AACCTCAGTGGCGCATCCCTAGCCGATGCAATCCTTTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACTCGACCAGGGAATCGGGAACCGATACCCCATCTAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GACCGTCTCGCACTTCGAGACGAGCATTGTTTTGTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CAAGTCCCTCGAAGAGGTAGCGGGCGAGATGAGATAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGTATTCACGCGCTTTAAGCGCGTAGTGGTCCCCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGGTACTAAAAGAGATACCATCGGGGTAGGCGAGAAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGCAAATTGGGGAGGTAGAAAAGGAAGGAACTAAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GATATAGACAATAAGTTTCTGAATCGCCACCACCACC
TTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAAGATGAACAGCTCAAATTCACTTCACTCAAGTTCG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTACTCCTTATACAACCCCAAAAGCTTAGCGCCCATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGATCTTCCATTTATTGGAGCAGGAGGGGCGTCCCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAATAGTTCCTCGAATAGAGCATACTTATGCGCGAGGAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAGGCGCGCAACCAAACCCTAGACGCCGAAAGGGAAATAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTGAATCATCTTATTCGTATCCTCCGCCGATCGCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTTTCGCCTCGATTTCCTTGTCGATCAGGTCTAGATTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGCAAGAAATAGTGAGGGTAGGGATTTCGTGAGAGAGGGTTTCCGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGATTGAACTAGATATCTTAATCCACAGGTATATC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAGAGACCCAACAAGGAGGTATTACAGGTAAAGGTTTAAT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AATGAATTAAAGTTCGACGAGACGATCTCGGCGAGA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACGGCATACTTCGCCGATCCTATCGAGCCATCGTCC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GGCTTCGTATGCCTGCTGCATTTCCACAGGACGATCATCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATATTCCGCTTCAAGCGTTCCCGTCATCGATTCCAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGCACAGGAGCCAATGCGTCGCATCGCCGTCGTCGC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GAAACTTCCGTTGCCGTAGCGCTGGCTGGAGGTTTC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTCGTCTTGGAACGCCGAGGCAAACCCCATTGAGTAA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGAACCCCAGCAACCCAGTAGCCTCCCTCCCTGCTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GTCAACCGATAATTTGAGGCCAGGAAACACCTTGGCGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTATCCTCCGCCCCCTTCGTCCCCTTCCCCTTGTGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGTTGGGCTTTCCCCGAACCTGCCGGGGTTGGATT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CGAAAATCGACCCCATTATGAAACCTAGTTTCCCCTAAG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	CTTCTCCAACTGCATCATTTGAGCAGGAGAGAAGTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TAGCTCTGCTTAATCAGCAATAGGGTTCACATTAC
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	TTGATACGTTCTTGAACGAAAGAACCTTCGTATGCCAGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AGTCTCACTTTTTGCCCCAGCAGTTCGGCCTTCGT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ACCCGACTGGAAAGCTAGAGTCTGCCGATCTTTTT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAGC	ATAGGGGTCATTCAAAACGGCGGCAGCTTTTTCCA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	ATCGAACTGACCCGCTTGAATGAGGCGATCGCACTCGG
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	AAAAAACTTATTCAGTGGACACAAGCGAATTACGATGTA
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAC	GCGGGTGGCTAGCGAGTGGTTGCCGCGTGCCT
CTTTCAATTCAATGAATCCCGGCAACGGGATTGAAAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168568028.1\|1050974_1051154_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568024.1\|1040773_1041622_+\|CRISPR-system-precrRNA-processing-endoribonuclease-RAMP-protein-Cas6	cas6	pfam10040_cas6_CAS-III:CAS-IV	gnl\|CDD\|227838
NZ_CP051167.1\|WP_168568035.1\|1058004_1058469_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568020.1\|1033800_1035924_+\|type-I-D-CRISPR-associated-helicase-Cas3'	cas3	cd09710_cas3_CAS-I-D	gnl\|CDD\|187841
NZ_CP051167.1\|WP_168568030.1\|1052034_1054035_-\|serine/threonine-protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP051167.1\|WP_168568029.1\|1051136_1051835_-\|ATP-dependent-dethiobiotin-synthetase-BioD	unknown	unknown	gnl\|CDD\|234625
NZ_CP051167.1\|WP_168568019.1\|1032607_1033582_-\|WYL-domain-containing-protein	WYL	pfam13280_WYL_CAS-I:CAS-III	gnl\|CDD\|379100
NZ_CP051167.1\|WP_168568023.1\|1040007_1040784_+\|type-I-D-CRISPR-associated-protein-Cas5/Csc1	csc1gr5	cd09711_csc1gr5_CAS-I-D	gnl\|CDD\|274458
NZ_CP051167.1\|WP_168568022.1\|1038930_1039929_+\|type-I-D-CRISPR-associated-protein-Cas7/Csc2	csc2gr7	cd09709_csc2gr7_CAS-I-D	gnl\|CDD\|375747
NZ_CP051167.1\|WP_168568036.1\|1059169_1060132_+\|protochlorophyllide-reductase	unknown	unknown	gnl\|CDD\|180983
NZ_CP051167.1\|WP_168568031.1\|1054074_1054533_-\|GatB/YqeY-domain-containing-protein	unknown	unknown	gnl\|CDD\|370480
NZ_CP051167.1\|WP_168568033.1\|1056274_1056847_+\|IS607-family-transposase	unknown	unknown	gnl\|CDD\|225296
NZ_CP051167.1\|WP_168568027.1\|1049764_1050976_-\|amidohydrolase	unknown	unknown	gnl\|CDD\|349941
NZ_CP051167.1\|WP_168568021.1\|1035934_1038868_+\|type-I-D-CRISPR-associated-protein-Cas10d/Csc3	cas10d	cd09712_cas10d_CAS-I-D	gnl\|CDD\|187843
NZ_CP051167.1\|WP_168568032.1\|1055028_1056045_+\|ribose-phosphate-pyrophosphokinase	unknown	unknown	gnl\|CDD\|235072
NZ_CP051167.1\|WP_168571731.1\|1042133_1042715_+\|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	gnl\|CDD\|273040
NZ_CP051167.1\|WP_168568018.1\|1028921_1029608_-\|SAM-dependent-methyltransferase	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568034.1\|1056860_1057934_+\|transposase	cas14j	-	gnl\|CDD\|223747
NZ_CP051167.1\|WP_168568026.1\|1043715_1044009_+\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP051167.1\|WP_168568025.1\|1042741_1043719_+\|type-I-D-CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|274976

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168568029.1\|1051136_1051835_-\|ATP-dependent-dethiobiotin-synthetase-BioD	gnl\|CDD\|234625	PRK00090, bioD, ATP-dependent dethiobiotin synthetase BioD.	7.75142e-75
NZ_CP051167.1\|WP_168568020.1\|1033800_1035924_+\|type-I-D-CRISPR-associated-helicase-Cas3'	gnl\|CDD\|187841	cd09710, Cas3_I-D, CRISPR/Cas system-associated protein Cas3; Distinct diverged subfamily of Cas3 helicase domain. 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; Diverged DNA helicase Cas3'; signature gene for Type I and subtype I-D.	2.72936e-55
NZ_CP051167.1\|WP_168568030.1\|1052034_1054035_-\|serine/threonine-protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	8.77972e-61
NZ_CP051167.1\|WP_168568032.1\|1055028_1056045_+\|ribose-phosphate-pyrophosphokinase	gnl\|CDD\|235072	PRK02812, PRK02812, ribose-phosphate pyrophosphokinase; Provisional.	0
NZ_CP051167.1\|WP_168568019.1\|1032607_1033582_-\|WYL-domain-containing-protein	gnl\|CDD\|379100	pfam13280, WYL, WYL domain. WYL is a Sm-like SH3 beta-barrel fold containing domain. It is a member of the WYL-like superfamily, named for three conserved amino acids found in a subset of the superfamily. However, these residues are not strongly conserved throughout the family. Rather, the conservation pattern includes four basic residues and a position often occupied by a cysteine, which are predicted to line a ligand-binding groove typical of the Sm-like SH3 beta-barrels. A WYL domain protein (sll7009) is a negative regulator of the I-D CRISPR-Cas system in Synechocystis sp. It is predicted to be a ligand-sensing domain that could bind negatively charged ligands, such as nucleotides or nucleic acid fragments, to regulate CRISPR-Cas and other defense systems such as the abortive infection AbiG system.	1.32308e-15
NZ_CP051167.1\|WP_168568024.1\|1040773_1041622_+\|CRISPR-system-precrRNA-processing-endoribonuclease-RAMP-protein-Cas6	gnl\|CDD\|227838	COG5551, COG5551, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	5.98446e-12
NZ_CP051167.1\|WP_168568022.1\|1038930_1039929_+\|type-I-D-CRISPR-associated-protein-Cas7/Csc2	gnl\|CDD\|375747	pfam18320, Csc2, Csc2 Crispr. The Csc2 Crispr family of proteins forms a core RNA recognition motif-like domain, flanked by three peripheral insertion domains: a lid domain, a Zinc-binding domain and a helical domain. The CRISPR-Cas system is possibly a mechanism of defence against invading pathogens and plasmids that functions analogously to the RNA interference (RNAi) systems in eukaryotes.	2.41352e-176
NZ_CP051167.1\|WP_168568036.1\|1059169_1060132_+\|protochlorophyllide-reductase	gnl\|CDD\|180983	PRK07453, PRK07453, protochlorophyllide reductase.	0
NZ_CP051167.1\|WP_168568031.1\|1054074_1054533_-\|GatB/YqeY-domain-containing-protein	gnl\|CDD\|370480	pfam09424, YqeY, Yqey-like protein. The function of this domain found in the YqeY protein is uncertain.	2.01386e-53
NZ_CP051167.1\|WP_168568033.1\|1056274_1056847_+\|IS607-family-transposase	gnl\|CDD\|225296	COG2452, COG2452, Predicted site-specific integrase-resolvase [DNA replication, recombination, and repair].	2.65575e-53
NZ_CP051167.1\|WP_168568027.1\|1049764_1050976_-\|amidohydrolase	gnl\|CDD\|349941	cd08021, M20_Acy1_YhaA-like, M20 Peptidase aminoacylase 1 subfamily, includes Bacillus subtilis YhaA and Staphylococcus aureus amidohydrolase, SACOL0085. Peptidase M20 family, uncharacterized subfamily of bacterial proteins predicted as putative amidohydrolases or hippurate hydrolases. These are a class of zinc binding homodimeric enzymes involved in hydrolysis of N-acetylated proteins. N-terminal acetylation of proteins is a widespread and highly conserved process that is involved in protection and stability of proteins. Several types of aminoacylases can be distinguished on the basis of substrate specificity. Aminoacylase 1 (ACY1) breaks down cytosolic aliphatic N-acyl-alpha-amino acids (except L-aspartate), especially N-acetyl-methionine and acetyl-glutamate into L-amino acids and an acyl group. However, ACY1 can also catalyze the reverse reaction, the synthesis of acetylated amino acids. ACY1 may also play a role in xenobiotic bioactivation as well as the inter-organ processing of amino acid-conjugated xenobiotic derivatives (S-substituted-N-acetyl-L-cysteine). This family includes Staphylococcus aureus amidohydrolase, SACOL0085, which contains two manganese ions in the active site, and forms a homotetramer with variations in interdomain orientation which possibly plays a role in the regulation of catalytic activity.	0
NZ_CP051167.1\|WP_168568021.1\|1035934_1038868_+\|type-I-D-CRISPR-associated-protein-Cas10d/Csc3	gnl\|CDD\|187843	cd09712, Cas10d_I-D, CRISPR/Cas system-associated protein Cas10d. 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; Large proteins, some contain Zn-finger domain. Fused to N-terminal HD domain; signature gene for I-D subtype; also known as Csc3 family.	0
NZ_CP051167.1\|WP_168568034.1\|1056860_1057934_+\|transposase	gnl\|CDD\|223747	COG0675, COG0675, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	4.48724e-23
NZ_CP051167.1\|WP_168571731.1\|1042133_1042715_+\|CRISPR-associated-protein-Cas4	gnl\|CDD\|273040	TIGR00372, conserved_hypothetical_protein, CRISPR-associated protein Cas4. This model represents a family of proteins associated with CRISPR repeats in a wide set of prokaryotic genomes. This scope of this model has been broadened since it was first built to describe an archaeal subset only. The function of the protein is undefined. Distantly related proteins, excluded from this model, include ORFs from Mycobacteriophage D29 and Sulfolobus islandicus filamentous virus and a region of the Schizosaccharomyces pombe DNA replication helicase Dna2p.	7.43662e-31
NZ_CP051167.1\|WP_168568025.1\|1042741_1043719_+\|type-I-D-CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|274976	TIGR04093, hypothetical_protein_L8106_25395, CRISPR-associated endonuclease Cas1, subtype CYANO. 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 a clade of Cas1 limited to the CYANO subtype of CRISPR/Cas system and most often the type found there.	7.40881e-150
NZ_CP051167.1\|WP_168568026.1\|1043715_1044009_+\|CRISPR-associated-endonuclease-Cas2	gnl\|CDD\|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	1.37382e-24
NZ_CP051167.1\|WP_168568023.1\|1040007_1040784_+\|type-I-D-CRISPR-associated-protein-Cas5/Csc1	gnl\|CDD\|274458	TIGR03159, cas_Csc1, CRISPR type I-D/CYANO-associated protein Csc1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) is a widespread family of prokaryotic direct repeats with spacers of unique sequence between consecutive repeats. This protein family is a CRISPR-associated (Cas) family strictly associated with the Cyano subtype of CRISPR/Cas locus, found in several species of Cyanobacteria and several archaeal species. This family is designated Csc1 for CRISPR/Cas Subtype Cyano protein 1, as it is often the first gene upstream of the core cas genes, cas3-cas4-cas1-cas2.	2.75163e-56

>NZ_CP051167.1|WP_168568026.1|1043715_1044009_+|CRISPR-associated-endonuclease-Cas2
MKDLLYLIVYDLPATAAGNKRRQRLHDLLCGYGTWKQYSLFECFLDAKQFASLQIKIETLIKPAEDAVCIYVLDAMAVRKTIVYGMPPPRQETVTIV
>NZ_CP051167.1|WP_168568025.1|1042741_1043719_+|type-I-D-CRISPR-associated-endonuclease-Cas1
MSVLYVTQPNAVLSKKYEAFKLAIAAEDGSVNKQSIPAQTLEQIVLMGNPSITGEALCYALELGLPIHYLSIFGKYLGSALPGYSRNGQLRLAQYAAHEDPSQRLTLVKAIVAGKIYNQYNVLYRHGEKDNPLKQRRGAIAQQETLDQTRGMEGLAAREYFARWEAMLPGPWTFPGRHRRPPTDPVNALLSFSYGLLRVQVTAAVHLAGLDPYIGYLHETTRGQPAMVLDLMEEFRPLVADNVVLSVLAHKEIKPDDFTESLGAYRLADGARKAFLQAFERKLNAEFQHPVFDYRCTYRRAIELQARLLARHLQEGVPYKPLVVR
>NZ_CP051167.1|WP_168571731.1|1042133_1042715_+|CRISPR-associated-protein-Cas4
MMDDYLPLSYLNAWEYCPRRFYWEYVLGEMEENEHILMGTHLHRNIDRENVSREGNLLIHRQQWVWSDRLQVKGIVDAVEECETIRVPLEYKKGRMARHLNDHFQLCAAALCLEERLNCSIEYGEIFYHGNRRRERVEFTLQLRMATEEAIAAARQAVNELMPPPLKRLAKCRDCSLFNICLPKEVKKLHEFE
>NZ_CP051167.1|WP_168568024.1|1040773_1041622_+|CRISPR-system-precrRNA-processing-endoribonuclease-RAMP-protein-Cas6
MSVNLPAHSDSLYSIVVELRAIDSGQPPATLGRALHAQVLRWIELGNPEVSASIHDRQSSPLSVSGLIGNRRPTQTESGDYFIVRICILDGDIVQPLLRGLSEWGTEPLILAKFPFLMTRTYMFADSHPLASSSSYSALANIKESDSSIELNFTSPTSFKQKQDIQTFPLTELVFGSLQRRWNMFAPPELQFPKIEWEGVVSAYELRTHALRLEGGAEIGTQGWIRYRFRDSEQARMATILGQYAFFAGVGRKTTMGMGQTRVMEKKKAKGKPKRKFKKPYK
>NZ_CP051167.1|WP_168568023.1|1040007_1040784_+|type-I-D-CRISPR-associated-protein-Cas5/Csc1
MVLYYCQLTLHDNVFFATREMGILYETEQYLHNWALSYAFFGDTYIPLSYANLGQYIQKPGYLDPKFEQNLLYLNPQGIYVFPGFPQRYFYQINTFKAAQVNYYGRSKKFGEKGASRNYPINYGRAKELGVGSEYSTYIYSKKEIDLPRWIRLGKWMAKVKVDSHQIPDSAIALRSGTYACHHPLNPLDLPESQEILLYNRIVMPPVSLIAQAQLSGEYCELKGDDWDRFRRDFPELKAEVCLPVGVAYGAREIANVS
>NZ_CP051167.1|WP_168568022.1|1038930_1039929_+|type-I-D-CRISPR-associated-protein-Cas7/Csc2
MTQLNALKNEFANDFPRLASGHYVHFILLRHSQSFPVFQTDGVLNTARTQAGINTTDTISRLVLFKRKQTTPERLAGRELLRSVSLISGDPDAENYCQYNGEKSCKQCPDCIIYGFAIGDSGSERSKVYSDSAFSLSSYEQSHRSFIFNGPSEAGTMSEGGQMRNAINELDHVLPEVTFPTVETLRDPTYEGFLYVLGNLLRTRRYGAQETRTGTMRNYPIAILLTDGEIFSNLYFTQALYDELKGDLNAPIADLKTVANTVVNRLLEDEPIRISHKLMGNDLEQFLDEVSEIYKDEEQLTEMLANLYEQTETYCNHYGAKSSKRSGKSGKK
>NZ_CP051167.1|WP_168568021.1|1035934_1038868_+|type-I-D-CRISPR-associated-protein-Cas10d/Csc3
MQTLMQQLLLTSLDPETDPILCEYIDIILPAVEREFGSMTALGGDRDRHYNILCTLKDPLAAEKARNWSDRPDQNLCVHVLNALLLGWNLAEHHLPTSLSDEEKRLFCLGITLHDYNKYCHGQGEEAPKASEIDDILALCREIGARLNFSAFWPQWETYLSDIGFLAQNTQFKCGTNTYPSNWPEFAIADSRRLTHPLRHLLGWSDIAVHLNDPADIATETAGERLQEHLNLLGIRKTLVYHRLRDSLGILTNGIHNATLHYARELGWEAIVFFARGVVYLAPKNFSSPDLADLKQFIWEQIALILGNKMLDGDVGFRRDGKGLKVAPQTSELFPPAQLIRQLSDVIAARVNNAKNPATPKRLAKLVERGLITEDREKELLKGADLRSDRLAEFIIVIQREFLGNCEDYGPWMLEALDLATIFNPEDLQINIGGVNYGWYLAAAQYFSKNSTLDLEQTTELLAEIGDRLADWATENNSLPAYSSPTQEVFDRYLQYYLDFSGIKTELPPFGQELNAYAIAKTRKAKQPICSLSSGEFPSEDQLDSVVLFKPQQYSNKNTLGGSKIKRGISKIWSLEMLLRQALWSARAGKLEEQQPVFLYIFPAYVYAPQMIKAIRVLVEELKTVNLWEIRKYWLNHELEVSQLSHWLWLREDAEIGRFAKGSYDSKDLPFMATVYTTTLGETVTEAWVHPAFLATILPKLLGVRVVATASNVPLYRSDREFCGSAVLDGVAGFWSLLHCPSEVRTEQLDSVLTRLLVVYTLHLDNRAHQSDARWGALNRTVREVMTDVLNIFAIAREGLRRRQHDPSPEEVERYWNFARIWSDLDKTMQEKLNFITELVRQYRTFYQVKVTDSSHAILLPFSKVLETILSVPTQVNEEDLILQGAGLLKDAIDRQNIYTRPLMMDKSVDFATRQQQELEAIHRFVQTCVCDLFGTLYRGDRALLQENRNRLKSGAEFAYRWLALQEKNERDLASPS
>NZ_CP051167.1|WP_168568020.1|1033800_1035924_+|type-I-D-CRISPR-associated-helicase-Cas3'
MKLRLHGLHSQLNPGVGRCPLGCDRHCQVRERAPGLQPPPGATCPLSSHQAQTFAAVRFGDADLIFNKSATGDGKTLGGTLPTLLDPQFRLMALYPTIELVEDQTRQQQRYHELFGLQSRDRVDRLYGEELSRRVRERDSNKFQELLDAIYHTPILLTNPDIFHYITHYRYRQAAFDRALLPLALAEWPDLWMFDEFHIFGPHQEAAALNSLTLIRRSQQQRRPRRFLFTSATPKPDFIAQLARAEFKIAEIEGIYANETTPGFRQILQPVELEFVQLGDGDAVQWLVESADRLDRWLRGDRAGRGLIVLNAISSVNRAIAQLTERLPGVTVCEISGRIDRRERGRIQAQLQASPDPVLVVATSAVDVGVDFRINLLVFESSDAATVVQRLGRLGRHPGFSHYRAAILIPKQMPWVMPRLGEWGDRQEPVGRPELQEAIAIAFDPPKSFAEYRQKWGPLQAHGMLAEISRESNKVSEILRDRMREDLGRVYGDRFDRYRKCWFALGKNPVGKATQKELLRFRGATAIQAAIADGSRIYTYDLLRLLPYTWIERCDRETFLEAARTADCSPDAFDDRYIHVYLKVREWLDNRQSLSLQTQRDTDELKTCELTLLDRLAIVGHPQPEVSTCLQRRKLLAFLVPVHRSQPSSHWQVSYTLQLGPHFGLYRLTDAGGNAYACAFDRDALLLDALKFKLRRFCRTQPQSLIF
>NZ_CP051167.1|WP_168568019.1|1032607_1033582_-|WYL-domain-containing-protein
MGQKCTHITDALYILRKLTERPYPREELIVVLGEFLEQTDRKPGDVAQKLHRIVRELRDLGFAIDCAPHRPYTLVESNFPLILSATQRQSLYLAVQFLEDMGFATQAQQIAALVNLDATDAPPDIQVDFSPPTDYSNPDYEKILHALQDRCAQQYRYRIHYCNSQKQNLRLDLDRSEIRLHDGALYLFAFVPDWKPKPRGGRVHNVENNGLFRIDRIKSVGAPSTVGWVFSEFPTLKIRYRMSGPLATYKPRRVQERVVKRDLVRRYVEIETVEDYLFWFRQRIFRYGANARVLDPPWLAAEIGEELRRAAAQYQAGDSRENSS
>NZ_CP051167.1|WP_168568018.1|1028921_1029608_-|SAM-dependent-methyltransferase
MGLRLEKVVPWGRSFDEYRRMFALSDDDLDRRILDCAGGPAAFNAAMNRRGTPIVSCDPVYQFSAAEIARRIDETYPVIVRGVAEDRDRYVWGDIHSPEHLGEVRLAAMQQFLADFEQGLRERRYIAAELPNLPFNPGQFDLALCSHFLFSYSVPLSWDFHRAAIAQLCEIAREVRLFPLLDNHSGQTSIHLDPAIAYLQDGGYHVEICPVNYQFQQGGDRMLRITHP
>NZ_CP051167.1|WP_168568027.1|1049764_1050976_-|amidohydrolase
MLSTPLDRHCADESRLRPEIHNLQMTLVEWRRHLHQHPELGFKEVQTAEFVSKKLQEWGVEHQTGIAKTGIVATIRGSKPGPVLAIRADMDALPIQEENEVSYRSRHDGIMHACGHDGHTAIALGTVYYLSRHRDDFAGTVKFIFQPAEEGPGGAQPMIEAGVLENPRPDAIVGLHLWNNLPLGTVGVRSGPLMAAVELFRCTIFGKGGHGAMPHQTVDAIVVGSQVVQALQTIVARNVDPIESAVVTVGEFHAGSANNVIAGKAQLSGTVRYFNPKMEDLIRHRFAEIIAGVCHSHGARYDLDYWQLYPSVVNDRAIADLVRSVAEHVVETPAGIVPKCQTMGGEDMSFFLQEVPGCYFFLGSANESKDLAYPHHHPRFDFDETALGMGVEMFVRCVEKFCS
>NZ_CP051167.1|WP_168568028.1|1050974_1051154_+|hypothetical-protein
MSFFCKNEYSFSYFIQETTKLNHRQRSPLPRDPQKTPGNGDRPVYFLFYFFLYFLSLRH
>NZ_CP051167.1|WP_168568029.1|1051136_1051835_-|ATP-dependent-dethiobiotin-synthetase-BioD
MSALLITATDTDAGKTVLTTAIAAYWQRYCQDRALGIIKPLQSGTGDREIYRRLFDLDQSPEELNPLYFSAPLAPPVAAEKEGRRVELERVWPIFQQLEQRKALVLVEALGGLGSPVTPELTVADLARDWRLPTVLVVPVRLGAIAHTVANVALARQSGVELRGIVLNCTEARTEEEIADLTPIEAIESFVQVPILGVLPYFENAEDLSKLAAAAAQLDLERLLPISLVAKG
>NZ_CP051167.1|WP_168568030.1|1052034_1054035_-|serine/threonine-protein-kinase
MQPPIPTGTILQNRYRPIAILGQGGFGRTYLAEDLGRFNEHCALKEFIPSQSSAYAVEKAEELFAREATTLYQLEHPQVPQFRATFEENGRLFLVQDYVEGKTYRSLLEECKANGRAFSQGEVLQLMQQLLPVLEYIHGRGIIHRDISPDNIILRDRDRLPVLIDFGVVKELATRLQGSTPQATSVGKLGYAPSEQIQTGRAYPSSDLYSLAVTCVVLLSAREPQELFDDIQLVWHWQAFVKSPVSTELATVLNRMLSYKPGDRYQYAREVVLGLQPAIAAQPAIAPPAVAASSTSPSEMRTVAVGHSPASPANTTQPQISPATGNDGDDDAFWSNPIAIAAAMVLLAAIAGFGSWAIVSNTRNRQNEPPTPISTASPLFSDLDTPTAQPTPTPTASASPTKTPTPSPTDSPSPTASPTPSEPPELPPAEPSISTVALNLEGENAKSVQGNVKENEIIQYTIDAEAGDRLSAYLSGDGVLMNAIGPDRQPLPGASRGVSLWEGPLDRAGQYTIELLPLPGFPNSNFELNLRLQEASTPEPTPTPIATATPEPIPEPIPTVQPTETPRAAIDRERVPLPPQGRTTVSGTTSARQKRYLVSVRRGQALKVELLEGAVGLSIRYPDGTLVENAEKLVQWQGEVQVSGQYQIDVVGSGGIRYAIAIDVSE
>NZ_CP051167.1|WP_168568031.1|1054074_1054533_-|GatB/YqeY-domain-containing-protein
MSLKDRIAQDLKTAMKAKDKLRLETVRSIKKLLLEKEVSLRPSGQENLTEAQEIELLAQLAKQRRDSIEQYEKAGRTDLAEQEAQELSIIEEYLPRQLSNAEIEGIIDEIIARVGASSPKDMGKVMGVAMKDLKGKADGKKVQELVKAKLGN
>NZ_CP051167.1|WP_168568032.1|1055028_1056045_+|ribose-phosphate-pyrophosphokinase
MKALRGSAVIRSATLTRHPSLATVTDHSRLRLFSGSANTVLAQEVARYLGIDLGPMIRKRFADGELYIQIQESIRGCDVYLIQPSCYPVNDHLMELLIVIDACRRASARQITAVIPYYGYARADRKTAGRESITAKLVANLITEAGATRILAMDLHSAQIQGYFDIPFDHVYASPVILDYLASKELHDIVVVSPDVGGVARARAFAKKLNDAPLAIIDKRRQAHNVAEVLNVIGDVKGKTAVLVDDMIDTGGTITEGARLLRQEGARQVYACATHAVFSPPAIQRLSSGVFEEVIVTNTIPVPEDKQFEQLTVLSVANLLGETIWRVHEDSSVSSMFR
>NZ_CP051167.1|WP_168568033.1|1056274_1056847_+|IS607-family-transposase
MPKKYVTPKEAQAILGVSEKTLRNWDKQGKIRAIRIPSGHRRYDISSIAGKKNRARIIYARVSSHKQKADLDRQADYLLCLYPRAEVIKEIGSGLNYNRKKFKAILERVMSGDVEQLVVGHKDRLARFGFELLKWICELNHTELVVCNNTELSPEKEMVEDILAIVHVFSCRLYGLRKYKSQIKEDPGLP
>NZ_CP051167.1|WP_168568034.1|1056860_1057934_+|transposase
MTWRKWLAASRYCYNAGMARLRDTYFEGLKLPSAYDLRQVVMSKIPEWVNSTPFNLRGAAVLDAHAAFKNTPKEHKLRPKFRSCRQPVSSFKLQSQNWRGGTTYPTHKTESGIKLKELKVNASEEIPEAIPSDFNVILDRGRWFITYTVEEERLTNPHQQAIALDPGVRTFLTGFDGNKVIALGNGSISRIVKLCKRLDRIQSETAKAKGRDNKRKRFKRRKLARQLRIKIRNLVDECHKKTAAFLTSNYSQVMIPDFKSSSMVYRAKRKINHKTARSLLTWAHYRFKQRLVHQAVKRGCQVIEVTEEYTSKTCSKCGQIHNRLGGSKKFICPNCSHRIDRDANGSINVFLKTISGN
>NZ_CP051167.1|WP_168568035.1|1058004_1058469_-|hypothetical-protein
MKKSSRTFLRFAACNILVSSLTAWGLPALAQQDLQQRVNSIESVEQVKQELRQLFEWRDQCGTGSCFNSSSTGICETVAALDVRVNGQIVGGMISDDPGLPISEEDLDLMRLIFEQCKPTNYQYWNWPMMLHVWYVPSEEVDNEIKNRLGLFLR
>NZ_CP051167.1|WP_168568036.1|1059169_1060132_+|protochlorophyllide-reductase
MEQDRMKTAIVTGASSGVGLYATKALAKRGWHVIMACRNLEKAKQAAQDLEIPEENYTILHVDLGSLQSVRKFISDFRTTGRPLDGVVCNAAIYMPLIKQPLRSPEGYELTMTTNHLGHFLMCNILLEDMKRSPGTDKRMVILGTVTHNPDELGGKIPPRPDLGELKGFAEGFKEPITMADGKKFEPVKAYKDSKVCNVLTMRELHRRYHDATGITFSSLYPGCVADTPLFRNHYPLFQKLFPIFQKYITGGYVSQELAGDRVAAVVADPEYKQSGVYWSWGNRQKKNRQSFVQKVSPQARDDERGEKMWDYSLKLVGLA

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Crispr_ID: NZ_CP051167_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_6

1142532-1143088

TypeI-D

N:A

Consensus_repeat	Method
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA	CRISPRCasFinder
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAAC	CRT
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA	PILER-CR

7 spacers

c2c9_V-U4,cas4,cas6,cas3,csc1gr5,csc2gr7,cas10d,WYL

The CRISPR arrays of NZ_CP051167_6

>merge|NZ_CP051167|6|1142532-1143088|CRISPRCasFinder,CRT,PILER-CR
AAAACAATCCCTAAAAGGGATTTGAGTGAATTTCAACCCGAAACCGGACTTTTCGGTGCAACCGCAGGCGATCGAACAAGCCCGTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAACAGATGATTACTGTGAATGAAAGTGATTCAAAATATCTAGAGTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAAGCTTAAAAATCACCTATTCCCATCCTTTTCTGGGGTTCCCGTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAACGGGTTGTGGTGCGCCAACTGCCAGTCCTGTTGCTGTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAACGTCTCCTGTCTCGGCATAGTTGCCGAAGCTCGGCGTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAACAAAAAATCGCACGCTCCCCCTGGAATAGCCATTAGTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAACAATTCCGTTGGCGCCCGATCCGCTAATGAGCCAGGTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAAC

>NZ_CP051167|6|5|1142532-1143087|CRISPRCasFinder
AAAACAATCCCTAAAAGGGATTTGAGTGAATTTCAA	CCCGAAACCGGACTTTTCGGTGCAACCGCAGGCGATCGAACAAGCCC
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA	CAGATGATTACTGTGAATGAAAGTGATTCAAAATATCTAGA
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA	GCTTAAAAATCACCTATTCCCATCCTTTTCTGGGGTTCCC
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA	CGGGTTGTGGTGCGCCAACTGCCAGTCCTGTTGCT
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA	CGTCTCCTGTCTCGGCATAGTTGCCGAAGCTCGGC
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA	CAAAAAATCGCACGCTCCCCCTGGAATAGCCATTA
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA	CAATTCCGTTGGCGCCCGATCCGCTAATGAGCCAG
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA

>NZ_CP051167|6|3|1142532-1143088|CRT
AAAACAATCCCTAAAAGGGATTTGAGTGAATTTCAAC	CCGAAACCGGACTTTTCGGTGCAACCGCAGGCGATCGAACAAGCCC
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAAC	AGATGATTACTGTGAATGAAAGTGATTCAAAATATCTAGA
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAAG	CTTAAAAATCACCTATTCCCATCCTTTTCTGGGGTTCCC
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAAC	GGGTTGTGGTGCGCCAACTGCCAGTCCTGTTGCT
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAAC	GTCTCCTGTCTCGGCATAGTTGCCGAAGCTCGGC
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAAC	AAAAAATCGCACGCTCCCCCTGGAATAGCCATTA
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAAC	AATTCCGTTGGCGCCCGATCCGCTAATGAGCCAG
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAAC

>NZ_CP051167|6|7|1142615-1143087|PILER-CR
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA	CAGATGATTACTGTGAATGAAAGTGATTCAAAATATCTAGA
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA	GCTTAAAAATCACCTATTCCCATCCTTTTCTGGGGTTCCC
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA	CGGGTTGTGGTGCGCCAACTGCCAGTCCTGTTGCT
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA	CGTCTCCTGTCTCGGCATAGTTGCCGAAGCTCGGC
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA	CAAAAAATCGCACGCTCCCCCTGGAATAGCCATTA
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA	CAATTCCGTTGGCGCCCGATCCGCTAATGAGCCAG
GTTTCAATCCCTAAAAGGGATTTGAGTGAATTTCAA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168568077.1\|1138742_1139000_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568083.1\|1146398_1148699_-\|type-I-D-CRISPR-associated-helicase-Cas3'	cas3	cd09710_cas3_CAS-I-D	gnl\|CDD\|187841
NZ_CP051167.1\|WP_168568081.1\|1144912_1145512_-\|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	gnl\|CDD\|273040
NZ_CP051167.1\|WP_168568089.1\|1155027_1155531_-\|pentapeptide-repeat-containing-protein	unknown	unknown	gnl\|CDD\|224276
NZ_CP051167.1\|WP_168568072.1\|1127978_1129061_-\|photosystem-II-q(b)-protein	unknown	unknown	gnl\|CDD\|130221
NZ_CP051167.1\|WP_168568084.1\|1148691_1149474_-\|type-I-D-CRISPR-associated-protein-Cas5/Csc1	csc1gr5	cd09711_csc1gr5_CAS-I-D	gnl\|CDD\|274458
NZ_CP051167.1\|WP_168568080.1\|1143324_1144602_-\|transposase	c2c9_V-U4	-	gnl\|CDD\|223747
NZ_CP051167.1\|WP_168568075.1\|1133451_1135869_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|153085
NZ_CP051167.1\|WP_168568079.1\|1140467_1142456_-\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|223540
NZ_CP051167.1\|WP_168568085.1\|1149486_1150491_-\|type-I-D-CRISPR-associated-protein-Cas7/Csc2	csc2gr7	cd09709_csc2gr7_CAS-I-D	gnl\|CDD\|375747
NZ_CP051167.1\|WP_168568073.1\|1129186_1130185_+\|7,8-didemethyl-8-hydroxy-5-deazariboflavin-synthase-subunit-CofG	unknown	unknown	gnl\|CDD\|180485
NZ_CP051167.1\|WP_168568076.1\|1138187_1138733_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP051167.1\|WP_168568078.1\|1139207_1140128_-\|ornithine-carbamoyltransferase	unknown	unknown	gnl\|CDD\|234835
NZ_CP051167.1\|WP_168568086.1\|1150549_1153258_-\|CRISPR-associated-protein-Csc3	cas10d	mkCas0201_cas10d_CAS-I-D	unknown
NZ_CP051167.1\|WP_168568082.1\|1145537_1146395_-\|CRISPR-associated-endoribonuclease-Cas6	cas6	COG5551_cas6_CAS-III	gnl\|CDD\|227838
NZ_CP051167.1\|WP_168568074.1\|1130177_1130939_-\|3',5'-cyclic-AMP-phosphodiesterase	unknown	unknown	gnl\|CDD\|277347
NZ_CP051167.1\|WP_168568087.1\|1153379_1154231_+\|WYL-domain-containing-protein	WYL	pfam13280_WYL_CAS-I:CAS-III	gnl\|CDD\|379100
NZ_CP051167.1\|WP_168571737.1\|1137359_1138103_-\|HEAT-repeat-domain-containing-protein	unknown	unknown	gnl\|CDD\|224331
NZ_CP051167.1\|WP_168571736.1\|1136148_1137240_+\|ribonucleoside-triphosphate-reductase,-adenosylcobalamin-dependent	unknown	unknown	gnl\|CDD\|274169
NZ_CP051167.1\|WP_168568088.1\|1154367_1154865_-\|DnaD-domain-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168568083.1\|1146398_1148699_-\|type-I-D-CRISPR-associated-helicase-Cas3'	gnl\|CDD\|187841	cd09710, Cas3_I-D, CRISPR/Cas system-associated protein Cas3; Distinct diverged subfamily of Cas3 helicase domain. 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; Diverged DNA helicase Cas3'; signature gene for Type I and subtype I-D.	1.09787e-96
NZ_CP051167.1\|WP_168568081.1\|1144912_1145512_-\|CRISPR-associated-protein-Cas4	gnl\|CDD\|273040	TIGR00372, conserved_hypothetical_protein, CRISPR-associated protein Cas4. This model represents a family of proteins associated with CRISPR repeats in a wide set of prokaryotic genomes. This scope of this model has been broadened since it was first built to describe an archaeal subset only. The function of the protein is undefined. Distantly related proteins, excluded from this model, include ORFs from Mycobacteriophage D29 and Sulfolobus islandicus filamentous virus and a region of the Schizosaccharomyces pombe DNA replication helicase Dna2p.	3.23557e-48
NZ_CP051167.1\|WP_168568089.1\|1155027_1155531_-\|pentapeptide-repeat-containing-protein	gnl\|CDD\|224276	COG1357, COG1357, Pentapeptide repeats containing protein [Function unknown].	7.76769e-26
NZ_CP051167.1\|WP_168568072.1\|1127978_1129061_-\|photosystem-II-q(b)-protein	gnl\|CDD\|130221	TIGR01151, Photosystem_QB_protein, photosystem II, DI subunit (also called Q(B)). This model describes the Photosystem II, DI subunit (also called Q(B)) in bacterial and its equivalents in chloroplast of algae and higher plants. Photosystem II is many ways functionally equivalent to bacterial reaction center. At the core of Photosystem II are several light harvesting cofactors including plastoquinones, pheophytins, phyloquinones etc. These cofactors are intimately associated with the polypeptides, which principally including subunits DI, DII, Cyt.b, Cyt.f and iron-sulphur protein. Together they participate in the electron transfer reactions that lead to the net production of the reducting equivalents in the form of NADPH, which are used for reduction of CO2 to carbohydrates(C6H1206). Phosystem II operates during oxygenic photosynthesis and principal electron donor is H2O. Although no structural data is presently available, a huge body of literature exits that describes function using a variety of biochemical and biophysical techniques. [Energy metabolism, Electron transport, Energy metabolism, Photosynthesis].	0
NZ_CP051167.1\|WP_168568084.1\|1148691_1149474_-\|type-I-D-CRISPR-associated-protein-Cas5/Csc1	gnl\|CDD\|274458	TIGR03159, cas_Csc1, CRISPR type I-D/CYANO-associated protein Csc1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) is a widespread family of prokaryotic direct repeats with spacers of unique sequence between consecutive repeats. This protein family is a CRISPR-associated (Cas) family strictly associated with the Cyano subtype of CRISPR/Cas locus, found in several species of Cyanobacteria and several archaeal species. This family is designated Csc1 for CRISPR/Cas Subtype Cyano protein 1, as it is often the first gene upstream of the core cas genes, cas3-cas4-cas1-cas2.	3.34228e-63
NZ_CP051167.1\|WP_168568080.1\|1143324_1144602_-\|transposase	gnl\|CDD\|223747	COG0675, COG0675, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	1.48163e-30
NZ_CP051167.1\|WP_168568075.1\|1133451_1135869_+\|hypothetical-protein	gnl\|CDD\|153085	cd01676, RNR_II_monomer, Class II ribonucleotide reductase, monomeric form. Ribonucleotide reductase (RNR) catalyzes the reductive synthesis of deoxyribonucleotides from their corresponding ribonucleotides. It provides the precursors necessary for DNA synthesis. RNRs are separated into three classes based on their metallocofactor usage. Class I RNRs, found in eukaryotes, bacteria, and bacteriophage, use a diiron-tyrosyl radical. Class II RNRs, found in bacteria, bacteriophage, algae and archaea, use coenzyme B12 (adenosylcobalamin, AdoCbl). Class III RNRs, found in anaerobic bacteria, bacteriophage, and archaea, use an FeS cluster and S-adenosylmethionine to generate a glycyl radical. Many organisms have more than one class of RNR present in their genomes. All three RNRs have a ten-stranded alpha-beta barrel domain that is structurally similar to the domain of PFL (pyruvate formate lyase). Class II RNRs are found in bacteria that can live under both aerobic and anaerobic conditions. Many, but not all members of this class, are found to be homodimers. This particular subfamily is found to be active as a monomer. Adenosylcobalamin interacts directly with an active site cysteine to form the reactive cysteine radical.	8.62184e-78
NZ_CP051167.1\|WP_168568079.1\|1140467_1142456_-\|ATP-binding-protein	gnl\|CDD\|223540	COG0464, SpoVK, ATPases of the AAA+ class [Posttranslational modification, protein turnover, chaperones].	4.36273e-31
NZ_CP051167.1\|WP_168568085.1\|1149486_1150491_-\|type-I-D-CRISPR-associated-protein-Cas7/Csc2	gnl\|CDD\|375747	pfam18320, Csc2, Csc2 Crispr. The Csc2 Crispr family of proteins forms a core RNA recognition motif-like domain, flanked by three peripheral insertion domains: a lid domain, a Zinc-binding domain and a helical domain. The CRISPR-Cas system is possibly a mechanism of defence against invading pathogens and plasmids that functions analogously to the RNA interference (RNAi) systems in eukaryotes.	6.54644e-168
NZ_CP051167.1\|WP_168568073.1\|1129186_1130185_+\|7,8-didemethyl-8-hydroxy-5-deazariboflavin-synthase-subunit-CofG	gnl\|CDD\|180485	PRK06245, cofG, FO synthase subunit 1; Reviewed.	1.17262e-170
NZ_CP051167.1\|WP_168568076.1\|1138187_1138733_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	2.91174e-16
NZ_CP051167.1\|WP_168568078.1\|1139207_1140128_-\|ornithine-carbamoyltransferase	gnl\|CDD\|234835	PRK00779, PRK00779, ornithine carbamoyltransferase; Provisional.	0
NZ_CP051167.1\|WP_168568082.1\|1145537_1146395_-\|CRISPR-associated-endoribonuclease-Cas6	gnl\|CDD\|227838	COG5551, COG5551, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	7.05423e-37
NZ_CP051167.1\|WP_168568074.1\|1130177_1130939_-\|3',5'-cyclic-AMP-phosphodiesterase	gnl\|CDD\|277347	cd07402, MPP_GpdQ, Enterobacter aerogenes GpdQ and related proteins, metallophosphatase domain. GpdQ (glycerophosphodiesterase Q, also known as Rv0805 in Mycobacterium tuberculosis) is a binuclear metallophosphoesterase from Enterobacter aerogenes that catalyzes the hydrolysis of mono-, di-, and triester substrates, including some organophosphate pesticides and products of the degradation of nerve agents. The GpdQ homolog, Rv0805, has 2',3'-cyclic nucleotide phosphodiesterase activity. GpdQ and Rv0805 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.	1.485e-85
NZ_CP051167.1\|WP_168568087.1\|1153379_1154231_+\|WYL-domain-containing-protein	gnl\|CDD\|379100	pfam13280, WYL, WYL domain. WYL is a Sm-like SH3 beta-barrel fold containing domain. It is a member of the WYL-like superfamily, named for three conserved amino acids found in a subset of the superfamily. However, these residues are not strongly conserved throughout the family. Rather, the conservation pattern includes four basic residues and a position often occupied by a cysteine, which are predicted to line a ligand-binding groove typical of the Sm-like SH3 beta-barrels. A WYL domain protein (sll7009) is a negative regulator of the I-D CRISPR-Cas system in Synechocystis sp. It is predicted to be a ligand-sensing domain that could bind negatively charged ligands, such as nucleotides or nucleic acid fragments, to regulate CRISPR-Cas and other defense systems such as the abortive infection AbiG system.	1.30022e-17
NZ_CP051167.1\|WP_168571737.1\|1137359_1138103_-\|HEAT-repeat-domain-containing-protein	gnl\|CDD\|224331	COG1413, COG1413, FOG: HEAT repeat [Energy production and conversion].	2.99993e-21
NZ_CP051167.1\|WP_168571736.1\|1136148_1137240_+\|ribonucleoside-triphosphate-reductase,-adenosylcobalamin-dependent	gnl\|CDD\|274169	TIGR02505, RTPR, ribonucleoside-triphosphate reductase, adenosylcobalamin-dependent. This model represents a group of adenosylcobalamin(B12)-dependent ribonucleotide reductases (RNR) related to the characterized species from Lactococcus leichmannii. RNR's are responsible for the conversion of the ribose sugar of RNA into the deoxyribose sugar of DNA. This is the rate-limiting step of DNA biosynthesis. Thus model identifies NrdJ enzymes only in cyanobacteria, lactococcus and certain bacteriophage. A separate model (TIGR02504) identifies a larger group of divergent B12-dependent RNR's. [Purines, pyrimidines, nucleosides, and nucleotides, 2'-Deoxyribonucleotide metabolism].	8.72491e-120

>NZ_CP051167.1|WP_168568079.1|1140467_1142456_-|ATP-binding-protein
MNRASIATWERANSQYTIAVAAHIHRLLEQYVARKQNLSVDLPPLDNSLYENLGREMNPPPRLETLCQKFGLSAFERQIAIACMAMGLFPSFRGLCANAHGSPQMPYPTFTLAWEVFPEAHWSAFTPQGPLRRWQLLQLGSAQVVTLCPLQIDESILHYLMGEPYQDDRLAGIVRGFDPIESEISSLQPSHRQIAERVTAVLSAPTGSGVVPVVQLCGTSPVEKWAIARAAARAMQCPLKAIAVARLPDNLQELSQVMRRWEREVVLNQSLLLVDGDRLIVGDLPQTQNLLQLIEDTQTPLILLTGDRLHGAPASLVSFDVPKLSHQEQLAVWQQQLTQVGVELNGRLDRLVSQFNLNPAIIHTASLQLETHHPHDRIVEQLWDFCRLQARPHLDDLAQRIDCNATWDDLILPEKEKAVLADIAAHVKQRATVYETWGFAAKSSRGLGISALFSGQSGTGKTMAAEVLAREFNLDLYRIDLSAVVSKYIGETEKNLRRIFDAAETGGAVLLFDEADALFGKRTDVKDSHDRHANVEVSYLLQRMEAYRGLAILTTNLKNAIDQAFLRRIRFAIPFPFPDAQARSEIWQRIFPPQTPTNELDFKKLGKLSVAGGNIRNIALNAAFLAADAGEAIAMKHILKAAQSEYVKMEKTLTDSEVRGWV
>NZ_CP051167.1|WP_168568078.1|1139207_1140128_-|ornithine-carbamoyltransferase
MNPLQGRDFLSVADLSRAELHSLLDLAAQMKDGTIAPRCEKVLGLLFDKASTRTRVSFSVAIYQLGGQVIDLNPNVTQVSRGEPLPDTARVLDRYLDVLAIRTFAQETLRGYADYAKIPVINALTDLEHPCQALADLLTIRETFGQLEGVTLTYLGDGNNVAHSLLLACAMTGVNVRVATPENYLPDRTIVAQAEALAQGKSEVVVTRDAVAAVEGSQVLYTDVWASMGQEDQADRRIPIFMPYQVSEALLSHAEDEAIVLHCLPAHRGEEITDGAIEGSQSRVWDQAENRMHAQKALLASVLGAV
>NZ_CP051167.1|WP_168568077.1|1138742_1139000_-|hypothetical-protein
MAIFREYIAPLLIVLVFLVALLAVSARIFLPADMMAPAPIEEEVVPDEAQSSVSRSDSLADLPPSLSALVKGLPEEPSGMEWSVN
>NZ_CP051167.1|WP_168568076.1|1138187_1138733_-|GNAT-family-N-acetyltransferase
MSQQLPQGYWLREGGRHDRPQLLQFLKSSYRELFGDRDLSHLRQTVEQYWSPQTPVWWVESPRDRSREGDRPDNAIVAGLWLGNALDQVTGDRYAHIFLVYVVETHRQRGIGSALIRHAEHWARQRGDRQIGLQVFIDNPPALNLYRKLGYRSQSLWMLKPLDRPEASTPHPTDRSSQGDC
>NZ_CP051167.1|WP_168571737.1|1137359_1138103_-|HEAT-repeat-domain-containing-protein
MHDDDLSALNTEDEFESPLDRWEETEAPKPDPEEMLPLLESSNPQQRTIAARAFCELQDARAIPALIRLLQDACPLVRVSAAYALGRNASPEVVEPAIAQLGREWNGYVRKGLVWALGNCHDRRSLAPLIDALKTDIAAVRLWAASSLGQLATVGYDIVVAAVPSLIEALLKDPVPAVRSNCAWALGQLCRELPSNVVYAGAIDSLIEALENDEDMGVREDAKSSLLRVGDPRGLQIIEDLEFEGLL
>NZ_CP051167.1|WP_168571736.1|1136148_1137240_+|ribonucleoside-triphosphate-reductase,-adenosylcobalamin-dependent
MEIIGCDFHCNLSEIHLNQIDPQDHKTQDDAFRAGALSVAVLLNHEFVEPRYRYSRQLDPIVGVSFTGLFDFFVHAFGAEWLHWWKEGRPDTPVGREFKRQEREYLSRWNRVVHETVWDYCDRHGLKRPNRCTTVQPSGTKSLLTGASPGWHPPKAQRFVRRITFRKYDPVAMACIDYGYNVVPSQSDKDENDNLLDDPFDDRCTEWLVELPVEVSWANLPGTDGIDVSKFSALAQFDFYMQVQRYWTTHNTSATIELTNEEVEPLGRRIYEAIRDDEGYISAALLARFEDLQTFPRLPFEPISKEVYEQLNREVVKRRKVEDFHQAMSLYDSGYSEESGPAGCDSDKCLFSDPKDVKESENY
>NZ_CP051167.1|WP_168568075.1|1133451_1135869_+|hypothetical-protein
MVRELERTRHNSDFPENAPTANPVFFRTYSRRRQDGTRETWQQVCDRTIAGLGKLGKLSEGELSLLHRMQGQLKSLSSGRWLWVGGTEWIEQPQNFSGAYNCSSTNISDWRAFGLLMDLAMMGCGTGAVLEPRYIEQLPPIRNRLDVRIVGTVGTTPKENRREETEVIVDGSRVTIAVGDSRQGWVKSYQSLLELSSDDRFDGEIDICVDLNDIRPAGETLKGFGGVANPVKLPQLYQRCAAILNKAVGRKLNSVECCLLIDEAATTIVAGNIRRCIAYGERVSAISGMKPIQDIAIGELVLTSSGQYKPVTNKFVQGVQNVVEIRTRETAIRCTANHRVAVYNGLQSYTWKYAGELQPGDRLISVPHRKGMPCSTTDYAWLVGFFIGDGHADIASAKRRNGGGGCVTFAFSRERLNGPLGQKCLRILKSLGYTPAISFRENQSYIKVHRKDLADELVQYKQPWETPIIPEFVWLGTEDIRGAFLAGLADADAGPSRNVLLHSTKIEFLRQVQRLSLSLGIATTLHERSPKTLKNRDTVYEGCHWLKIRGIQSQVNAVALVNPHMGREGFRICGQKKNGLSLPHQFIEEAMTAGWRAKTVNNTKSIINPSKKGGSMRDANWDTLLAEGVVHPHWLPLEVQLVVPAGQAETFDIEVESDREFIASGLLVHNSAGMRQFDSNDELAGVAKENLWQQTPEGNWRIDPERDALRMANHTRVFHRKPSRQECIDAVRKQYYSGEGAIQWAPEAIARANCDLLADDTLKRDFIAAYSEGNGADWFQNAFPNLDESERQHRLARFGLNPCGK
>NZ_CP051167.1|WP_168568074.1|1130177_1130939_-|3',5'-cyclic-AMP-phosphodiesterase
MIQTLPLHVAQITDLHLFSDRNKRLMGIDTAASLQKVLSCLRQLRHPQDLLLLTGDLSQDETPESYELLVDLLSPWDIPSYWIPGNHDDPSLMEQILKTPPFFTDKVVEAGNWSLILLDSTVTGWVSGQLSPSSLDWLEWQLERSRDRPTLIGLHHPPFAVNSEWIDSIALQNPDDFFAIVKGHPQVKLVLCGHVHQNFCHQQKYLRCFTTPSTCVQFKPGSAEFAVDSAQPGLRLFNLYPDGTWETKVMRVS
>NZ_CP051167.1|WP_168568073.1|1129186_1130185_+|7,8-didemethyl-8-hydroxy-5-deazariboflavin-synthase-subunit-CofG
MNNISSAYNSRRLLTYSPAYTVVPTYECFNRCSYCNFRRNPGESPWLSLEEARVRLEAIADRGVIEILILSGEVHPGSSRRSPWIRHLHDLGQLALDLGFLPHTNAGPLSYEEMAQLKQVNVSMGLMLEQVTPQLLETVHRHAPSKVPTLRLQQLEWAGELRIPLTTGLLLGIGESPGDRRQTLEAIARVQQRWGHIQEVILQPHRPGSRQQEALPGFDDRALPDVVAMARAILPENIRLQIPPNLVAQPDILLACIEAGARDLGGIGPHDEVNPDYPHPAIAQLSEIVEPLGWHLDRRLPVYPAYYRWLTPSLKRAVDRWNGEIGSALPVN
>NZ_CP051167.1|WP_168568072.1|1127978_1129061_-|photosystem-II-q(b)-protein
MTTTLQQRESASLWDRFCEWVASTENRLYIGWFGVLMIPTLLTATTCFIIAFIAAPPVDIDGIREPVAGSLLYGNNIISGAVVPSSNAIGLHFYPIWEAASLDEWLYNGGPYQLVIFHFLIGVFCYMGREWELSYRLGMRPWICVAYSAPVAAATAVFLIYPLGQGSFSDGMPLGISGTFNFMLVFQAEHNILMHPFHQLGVAGVFGGALFSAMHGSLVTSSLVRETTETESQNYGYKFGQEEETYNIVAAHGYFGRLIFQYASFNNSRSLHFFLAAWPVVGIWFTALGISTMAFNLNGFNFNQSIVDSQGRAIGTWADVINRANLGMEVMHERNAHNFPLDLASTDATPVALTAPQING
>NZ_CP051167.1|WP_168568080.1|1143324_1144602_-|transposase
MLNMTWEFKLEPTAEQVCEIEHILDVCRDVWNFALRERKDWLSSRKSPVNACSIRQEFILPADEPFPSYHVQSKRLTVAKSKYPRLKTVNAQVLQQVLQKLEASWESWRLKRSGLPRFKKPNRMRSFVFPQMLKNCIPPTPLGKGGEGGIKLSQLGWVRVRWSRKIPNLFQAKQARIVRKASGYFVMLSLQADVDIPDVAPHGHPVGIDVGLEYFLSTSDGEQVKRPRFFDNLHRKLKLLQRRLKNKQKGSANWLKLQRKIARVHQRIADTRKDWHFKLAHRLCDSAGMIFVEDLDFRIMAKGMLGKHTLDAGLGQFVNQILPWVCWKRDVYYGKVDARGTSQECPDCGAEVRKDLSTRIHYCHNCGSIKPRDVASGQVICTRGQRGIKNACGVEATGDRVTDSSWLAVKQEIFGATQGISTHNL
>NZ_CP051167.1|WP_168568081.1|1144912_1145512_-|CRISPR-associated-protein-Cas4
MTEMLTEVAIASLNHFTYCPHRCWRMFCAGEFVENAYTVEGSTLHDRVHTLGEGFREDTWQVRSIWLKSQKYGLVGKADLVESKAGEIYPVEYKRGRKNPWENDALQVCGQALCLEELTGRSIPTGYVYSLQSHQRQDIVLDDKLRRETIATIESVRQMLQTGEMPPALYYTTSCRGCSLYGGCLPQAASKVERYQEIG
>NZ_CP051167.1|WP_168568082.1|1145537_1146395_-|CRISPR-associated-endoribonuclease-Cas6
MPHSLVFNFLPENPIYPEYATGRHLHALFLTAVNAVDSQLATHLHETKTEKAFALSPLQVVRHPRRNQRASVPPILQFQHRYPIQPETPCWWRVSLLDDSLFRKLSHLWLNLNSGQPWHLGAANLHVTSILGTPQSTQPWANAASYAELYENASDRNRRISFQFSTPVAFRQQKYDTALPSPESVFKSLLNSWKKYSTIELPEFSTESIFPCFFKLNTEIAEFEFRKKGKSGKFIGAVGSIDYRILGDVSTATIQTLNTLADYALYSGIGRKTTMGMGMARKMDR
>NZ_CP051167.1|WP_168568083.1|1146398_1148699_-|type-I-D-CRISPR-associated-helicase-Cas3'
MNNLHITLEPAQIAACTETDLPDALKKVFGGKALQHQVDVYNAAKDHDLILDLSATGTGKTKAGFSVVLENPTRNVVYVAPTNALVEQQTIAAEKFVKAAGLPHVVKAASAKHVNSWPNDRVGRRAGEKIYNVLQDPSTLFPECGGGRPVLLVTNPDIFYYAAFFQYNRRDRSNIASIFYKSFATVIFDEFHLYDAKQLVSLLFYLAVSHVFGYFQNNRKVVLLTATPEPACEEALKTLETDGVRVALIDGNGKTGHLIPSQTAVNLEVRSYPEKDEIIREIVGEVCDRIQNRPDDNGAVILDSKDTLNAISTELRDRGYEHYCGRITGDTPKEDRPKAAQKQVILATSTVDVGFNFEREIERDRQNLDWLIFSSRDRFSFWQRIGRVGRVLGKVKTDISSHAIVYLPQEVWQQGLQNLDGSGGREALQKTLESLECMQRPFLNIYWRSEAFLEIARPLLELETSLINTPGEHLISQLYQTLQSVLGGNRPWKEYRQRMKILQGAENIAKTKIEKIPKDWKYIKGGQNCVKSFLKAYCSEDWEDVKSGRVAIEQLEQEILSQRYYTEKLKHYARILQISYAPLFRFRDSLFENVKIEDPKGFLLDNCGETNLDPLHLLRFYEFVSDGDRILVTERAKQPYNLSFSLNLTNLNIDLDEFANTQLSKLYAFQNCQIQRGIGEMMRSTAIIAELTPPLLPGVIVKEHLNNRWAIFKLKKQGLDCYPITVCDNFGREEKYTFFPSLSGILAIATAGFALKCPDNEEFWCV
>NZ_CP051167.1|WP_168568084.1|1148691_1149474_-|type-I-D-CRISPR-associated-protein-Cas5/Csc1
MPQSELNLSDSPTFTTARLVELWCAEPVFFASRELSDTYYTEGAIGNYALAYALGWARAPYRLTGKDTGRPRYREDLTPLAGQHYILPAWPVENSPSYRFERFNALSDAYWYAMTNNRVATAREDLPLKRTGKKPNTYRPSNFPQTGRLRIIDRGNRFQTLVFGEGELPEYIRVGKFTSKVRVDVGEALPVRQLPADTYRCNTYLNSADLPPDLEPFAFDLIAIPPASLLKNLQFHGEAWQIGNFLIPANLEFLGGNSRE
>NZ_CP051167.1|WP_168568085.1|1149486_1150491_-|type-I-D-CRISPR-associated-protein-Cas7/Csc2
MSIEKLQSFLAPNYENFPKGRTIGVVVLRTTQSETIFRTEGTGEPMCRESVQAGVQNTESILRLVMTKRKQVAPERRRGREFLRNHELLYTAPKSDSPCSLNTNAPCEMCVDCFLYGFAAGGEGAQKSRIWTEDAFSVLPSTELIGDRTINAVFETGTMRDEKGNASTALKTSEYIKPGVHFLDIATLKDVTADELRYALGNLLLTTRYGAVSSRVGRMENQILGVFGGISELPSSLELVQGVYDRLIAENVALEHPLNTNALIEATQSVINTWTNKRGISMQLSSEELDALIEDIDRHWSLDEQETFLKRLDESYQPYRQIKQQSTKKGRKNK
>NZ_CP051167.1|WP_168568086.1|1150549_1153258_-|CRISPR-associated-protein-Csc3
MARLADLLPGQPKSLDERYFSEIRPKLYQHHGKHAQHGTRRGRSLAEHLDSACQFVLTVSKIAGVPEDKRSQILAATAVHDLNKFDEKGRNVKTLARDRTFLREQLDRAYVADLVKNDADLERVRRLIERHSDHNVSDGMRFLPEDPEIDRWSAMVVAADLFDLGIDDNLRIRKVENKLTIALQRPCRLFRISLAEDRGYFTSLLLSACEKVLCDRGLTTLAIEPNGQIFLGETFPEADIAPDIARHWQKQIDRTFGSNVKQLVKPSKDGIKIDTQAVQQNPDAALDAVDELLVKKASSYKADKVRETIEKYGNDAGEDALTAAAQLGLQPVSNAEEFAISEGLKSLYLSYREAEINPKEAWNRIAEQVGISPEQRTALEPFNPQYGRGLFAAKVVSGGLPTIYEALKESFQLRTTDEVEASQELIDAVRQLLNFPTTKPLPGIQELTAYIDANPRKRCSLGTTSNQIEELISSKMPPETKVQAFSNRLPGGMSAEPKRRGDTLSALAYQLMAVGANFPKSVKQEPVYLHFALPSGSNVELRRIWREFLKKTAQINEDGTVTVDELELYRKNETIFKANKVVGFAFPKRPDFVNSTVTIPVLWGDVNNSVALLKSLRLALELSLSFEMGFPFILSSNLEIKPTWNDFGQVEGIPSSLQPLLGSGQYLRDGHLAEKERQKTLTAEDVLERLRCVGELAISVASLQKKDDCLYDLARATTRPLNLYYVLLRWVLREQDDPNLEAVWRRIREPLHQLLENLMSDEHTRISDYLKQAAKIAETGKLRGSSFRRTAQSEPFSEFIKAVRSKKSHMDWDTVFAALVQQYHTRLDRIREHGVGATKYEQVKQFYEVLKKLFEEVYNSRPERLLTDSKTLEAAYLFFLQEARQELKAKNEESSEVQPEAK
>NZ_CP051167.1|WP_168568087.1|1153379_1154231_+|WYL-domain-containing-protein
MARKKETITLSIPPGTKARLEAIARRLGIMWGKSPSISGLIVAIAEEEYELGETFVLTPRQLAVLQQATDLLIDTGFVDKAQTLLQLMLDRGDLDPSFHQELMRTIGQTGQPWRVVVEEHRKNRQPFRVLYRNSQGEEYTYTVRYAQFDFHEKRYYLHVWCDETEDVQDSQFPELRHNRCLRLDRIQSIVPTDASWREEGLDTIKVHLHFYSGMVKAYEPKKDIDIEDREVNGVRQVVRRVANPFWLARDIRRYGEDCEVIAPDSLRQLMMQEYRKMLDRYSS
>NZ_CP051167.1|WP_168568088.1|1154367_1154865_-|DnaD-domain-protein
MMTPSASLPSSPTPESNPSDLQSGEERPIDQTTLLSTQGLEKDSDWLGEKLHDLCDELGLSKPEDLIAIVVQWAHVEKEASIERELNQVKKVLDDSIDLGILTKEEAIERLEKKRKDLKKPPLLDALLNNKEQETLYRILMDSQSDIEAIREEIRIIIRLFFGKQ
>NZ_CP051167.1|WP_168568089.1|1155027_1155531_-|pentapeptide-repeat-containing-protein
MAGVAMKIYAIPTLSLLAPLTLVTSAWAQPSSADVEKLIQTKACQRCNLNGADLSGIDLRGVDLTYANLIGADFSRSNLSTANMRGADTTGANFQMADLSRANLSTTNLSTANLLGSNLIEANLDSADLSQANLYGADLRGANLTDADLDEVNLLGANLEGAIGLRR

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Crispr_ID: NZ_CP051167_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_7

1409731-1409904

Orphan

N:A

Consensus_repeat	Method
GTCGGCGTCGGCGTCGGCGTCGG	CRISPRCasFinder

3 spacers

The CRISPR arrays of NZ_CP051167_7

>merge|NZ_CP051167|7|1409731-1409904|CRISPRCasFinder
GCTGGCGACGGCGACGGCGTAAACGGGTTTGGGATGAGCGGCGATCGCCCGTTGCAGGGTAAAGGTTGTAGGAGAGGTTGTCGGCGTCGGGGTCGGGGTCGGCGTCGGCGTCGGCGTCGGCGTTGCGGTTGGTGTCGGCGTCGGCGTAGGGGTTGGGGTTGCGGTTGGTGTCGG

>NZ_CP051167|7|6|1409731-1409904|CRISPRCasFinder
GCTGGCGACGGCGACGGCGTAAA	CGGGTTTGGGATGAGCGGCGATCGCCCGTTGCAGGGTAAAGGTT
GTAGGAGAGGTTGTCGGCGTCGG	GGTCGGGGTCGGCGTCGGC
GTCGGCGTCGGCGTTGCGGTTGG	TGTCGGCGTCGGCGTAGGG
GTTGGGGTTGCGGTTGGTGTCGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168568268.1\|1406880_1408377_-\|polyphosphate:AMP-phosphotransferase	unknown	unknown	gnl\|CDD\|274736
NZ_CP051167.1\|WP_168568266.1\|1404346_1405360_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|223843
NZ_CP051167.1\|WP_168568277.1\|1424794_1425241_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|379267
NZ_CP051167.1\|WP_168571763.1\|1413622_1415026_+\|flagellar-motor-protein-MotA	unknown	unknown	gnl\|CDD\|224212
NZ_CP051167.1\|WP_168568261.1\|1397432_1398494_+\|3-deoxy-7-phosphoheptulonate-synthase	unknown	unknown	gnl\|CDD\|237376
NZ_CP051167.1\|WP_168568260.1\|1396789_1397245_+\|DUF3464-family-protein	unknown	unknown	gnl\|CDD\|371813
NZ_CP051167.1\|WP_168571764.1\|1425404_1425896_-\|pentapeptide-repeat-containing-protein	unknown	unknown	gnl\|CDD\|224276
NZ_CP051167.1\|WP_168568276.1\|1421610_1424088_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP051167.1\|WP_168568263.1\|1400348_1401476_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568262.1\|1398622_1399738_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377474
NZ_CP051167.1\|WP_168568267.1\|1405989_1406847_+\|pentapeptide-repeat-containing-protein	unknown	unknown	gnl\|CDD\|224276
NZ_CP051167.1\|WP_168568271.1\|1415044_1415515_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568273.1\|1416764_1418186_+\|pyruvate-kinase	unknown	unknown	gnl\|CDD\|223545
NZ_CP051167.1\|WP_168568264.1\|1401672_1402428_-\|parvulin-peptidyl-prolyl-isomerase	unknown	unknown	gnl\|CDD\|275293
NZ_CP051167.1\|WP_168568272.1\|1415607_1416315_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568265.1\|1402510_1404256_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP051167.1\|WP_168568270.1\|1411197_1413048_-\|DUF3352-domain-containing-protein	unknown	unknown	gnl\|CDD\|371750
NZ_CP051167.1\|WP_168568274.1\|1419020_1419989_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571762.1\|1408594_1408891_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568275.1\|1420062_1421436_-\|VWA-domain-containing-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168568268.1\|1406880_1408377_-\|polyphosphate:AMP-phosphotransferase	gnl\|CDD\|274736	TIGR03708, poly_P_AMP_trns, polyphosphate:AMP phosphotransferase. Members of this protein family contain a domain duplication. The characterized member from Acinetobacter johnsonii is polyphosphate:AMP phosphotransferase (PAP), which can transfer the terminal phosphate from poly(P) to AMP, yielding ADP. In the opposite direction, this enzyme can synthesize poly(P). Each domain of this protein family is homologous to polyphosphate kinase, an enzyme that can run in the forward direction to extend a polyphosphate chain with a new terminal phosphate from ATP, or in reverse to make ATP (or GTP) from ADP (or GDP). [Central intermediary metabolism, Phosphorus compounds].	0
NZ_CP051167.1\|WP_168568266.1\|1404346_1405360_-\|hypothetical-protein	gnl\|CDD\|223843	COG0772, FtsW, Bacterial cell division membrane protein [Cell division and chromosome partitioning].	0.00473562
NZ_CP051167.1\|WP_168571763.1\|1413622_1415026_+\|flagellar-motor-protein-MotA	gnl\|CDD\|224212	COG1293, COG1293, Predicted RNA-binding protein homologous to eukaryotic snRNP [Transcription].	5.75876e-05
NZ_CP051167.1\|WP_168568261.1\|1397432_1398494_+\|3-deoxy-7-phosphoheptulonate-synthase	gnl\|CDD\|237376	PRK13396, PRK13396, 3-deoxy-7-phosphoheptulonate synthase; Provisional.	0
NZ_CP051167.1\|WP_168568260.1\|1396789_1397245_+\|DUF3464-family-protein	gnl\|CDD\|371813	pfam11947, DUF3464, Protein of unknown function (DUF3464). This family of proteins are functionally uncharacterized. This protein is found in bacteria and eukaryotes. Proteins in this family are typically between 137 to 196 amino acids in length.	9.43234e-66
NZ_CP051167.1\|WP_168571764.1\|1425404_1425896_-\|pentapeptide-repeat-containing-protein	gnl\|CDD\|224276	COG1357, COG1357, Pentapeptide repeats containing protein [Function unknown].	3.0497e-26
NZ_CP051167.1\|WP_168568276.1\|1421610_1424088_-\|PAS-domain-S-box-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	4.64751e-47
NZ_CP051167.1\|WP_168568262.1\|1398622_1399738_-\|hypothetical-protein	gnl\|CDD\|377474	pfam05157, T2SSE_N, Type II secretion system (T2SS), protein E, N-terminal domain. This domain is found at the N-terminus of members of the Type II secretion system protein E. Proteins in this subfamily are typically involved in Type 4 pilus biogenesis, though some are involved in other processes; for instance aggregation in Myxococcus xanthus. The structure of this domain is now known.	2.74146e-06
NZ_CP051167.1\|WP_168568267.1\|1405989_1406847_+\|pentapeptide-repeat-containing-protein	gnl\|CDD\|224276	COG1357, COG1357, Pentapeptide repeats containing protein [Function unknown].	2.4149e-39
NZ_CP051167.1\|WP_168568273.1\|1416764_1418186_+\|pyruvate-kinase	gnl\|CDD\|223545	COG0469, PykF, Pyruvate kinase [Carbohydrate transport and metabolism].	0
NZ_CP051167.1\|WP_168568264.1\|1401672_1402428_-\|parvulin-peptidyl-prolyl-isomerase	gnl\|CDD\|275293	TIGR04500, PpiC_rel_mature, putative peptide maturation system protein. Members of this protein family have a novel N-terminal sequence region. Close homologs to the C-terminal region of this protein score well to PpiC-type peptidyl-prolyl cis-trans isomerase models (see pfam00639), yet no sequence within the family scores well to such models, suggesting origin within a branch of the PpiC family but subsequent neofunctionalization with a rapid change of sequence. The genome context for members always includes an ATP-grasp enzyme associated with peptide modification and a short polypeptide likely to be the modification target.	2.20864e-15
NZ_CP051167.1\|WP_168568265.1\|1402510_1404256_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	4.34195e-148
NZ_CP051167.1\|WP_168568270.1\|1411197_1413048_-\|DUF3352-domain-containing-protein	gnl\|CDD\|371750	pfam11832, DUF3352, Protein of unknown function (DUF3352). This family of proteins are functionally uncharacterized. This protein is found in bacteria and eukaryotes. Proteins in this family are typically between 538 to 575 amino acids in length.	4.53573e-150
NZ_CP051167.1\|WP_168568277.1\|1424794_1425241_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|379267	pfam13565, HTH_32, Homeodomain-like domain.	3.0495e-06

>NZ_CP051167.1|WP_168571762.1|1408594_1408891_+|hypothetical-protein
MEEQQHHLNSIVKEIGEAVLATTETVEQLARRVDDLAVQVKQQSQQVQQQGYQIFALCDAVQTLAEGQDRSLERLVQLTDSVERLLGAIVEEEQEPTD
>NZ_CP051167.1|WP_168568268.1|1406880_1408377_-|polyphosphate:AMP-phosphotransferase
MLDTLDLSLSLDKPSYKEQIESLMRQLRQLQKACRDKKLPVIIVLEGWAAAGKGSLVQKMVGYMDPRGFIVHPIWPPSEQERQFPLLWRFWQKLPANGTIGFFYHSWYTHVLEDRLFGRVDDSEIPMLMREINAFERQLFDDGAAIAKFWIHLSRKELKKRLKKAAADPLDSWRVRPEDWQQAKNYQHYAALAEEMVIHTSTGPAPWTLVEGDCKRWTRVKVLTKMATTITEALDLRYCQVPPPSLPAQTELHPTEPDFLGQVDLSQSLTKAEYKKQLRQEQVRLRELQLKMHELQIPVIALFEGWDAAGKGGAIKRLTDILDPRSYVVSAFAAPTDEEKAHHYLWRFWRRLPTAGSFGIFDRSWYGRVLVERVEEFATEPEWRRAYREINEFEEQLVNAGYVLLKFWLHISAEEQLRRFQERQDNPFKQHKLTEEDWRNRDRWPLYYVAVNQTIQRTSTPLAPWTVVAGDNKYYARVQTIKTVVAAIEQELDRRRSA
>NZ_CP051167.1|WP_168568267.1|1405989_1406847_+|pentapeptide-repeat-containing-protein
MSIDYLLELYEKGIRDFSGLDLRGQNLSGITFVQVNLSNAYLDGADCTRAFLTKANLSHAALNRANLSFVKLSDANLTGAQLRKADLHGAFLVKSRLSEAQMSGANLAGANLREADLSGANLCGANLEGINLRGANLKGANLRWANLGGARLSGACLQGACLTGGQLTGAFLNGADLEGVDLDGVNLSWAKLSGANLAGAKLMSANFWGAKLRNVNLTGANLSGANLSRALLEGVQLRAANLNEAIVDDRLLETTIALPSWEGRRSLSMPRPAWKARETTVSVGC
>NZ_CP051167.1|WP_168568266.1|1404346_1405360_-|hypothetical-protein
MFLLIAQILLWVLLGLAIWFVLLRLIPKEYLTWLGGAILLTVIILAFFFPTDRSIATIWNIISLPLKPLGLTLLLLILGTKKKKESKLIWAAVAILLLSSIPWLADRYEYGLIRSNLAVQTNVCTARTVSEADAIVLFSKGTTQPFLRYQPDLVAQQTSARIVEMARVYNELRTAGRLPQAIVVGRSTPFAWTVGQQTPNPNLEATTIARRFASLVGLPLGDIALLKGDTVREAATQVQDYLERRTDLGRRIVTISSSVDSPRVVSAFTQDNFVVIPRAPALDTVVCDRENEVVELEQLIPNAESVLQTSQVVDEFFTLIYYFLRGWIAPCADCWDN
>NZ_CP051167.1|WP_168568265.1|1402510_1404256_-|ABC-transporter-ATP-binding-protein
MSRSQLQKLGTYMRPHWRTATLGIAALFVVNALSVYIRRLIGNVVDRLQVSLDFDRVLFFVFVILSLATVMWVIRVASRMLLFGVGRQVEFDLKQGIFQHLLRLEPAYFSANTSGDLINRATSDVDNIRRLLGFAVLSLVNTIFAYGLTLPVMLAIDVKLTLWAIAVYPVMLILVQLFSDRLRSQQQLVQEELSSLSELIQEDVSGIASIKIYAQEENERNVFRQLNDRLLSANLKLAKTRSLLFPILGGLASLSLLILLVIGSGAIANGDISIGDFISLLLYVEGLVFPTALLGFTITAYQRGEVSIDRVESIFAVEPRIQDERKARSLQPPVAGRLSARELVYTYFGARQPSLDGISFEILPGETVAIVGPIGSGKSTLANAIPRLLDIAPGQLFLDGQDITELALNDLRGAIAYVPQESFLFSTTIRNNIRYGNPLASDAAVEDVAKQAQIYEEILNFPQQYDTLVGERGITLSGGQRQRMALARALLLDAPVLILDDALSSVDNQTATDILHNLSTGTNKKTVLFISHQMSAAASADRILVMDRGAIVQTGTHGELVRQSGLYQSLWEQQKFEEMLR
>NZ_CP051167.1|WP_168568264.1|1401672_1402428_-|parvulin-peptidyl-prolyl-isomerase
MDPEKFITIDEEQISLRQALEYLRKSGDLPQLLTRILRQYVLEQELQERSDLEVDPSRLEQVMVNFRLQNQLTDSPKFNQWLQSQGLTYATFREQMAMAVKVEQLKAETIADKVDDYFTQNQAFFEQVVLSRIVVSEVDKAAQLKGQVDENPQLFEALAKEHSIVADRVFNGMMGAIALNQLPPSMREALRQAEPGEIVGPLEHEGRYSILRLERRLPAKLEGQLKQTLEEQFFTQWWQQKLQNKKVKLNL
>NZ_CP051167.1|WP_168568263.1|1400348_1401476_-|helix-turn-helix-domain-containing-protein
MMVSEQLARKWRSRLAEECSQYSQSVRDSIVEWLLGEKRERFESVSPEKLKTICSGIDYRYQILRQRYLGVSPERGYTQLIRRLSSLVLLRNKIRTWVALSRDRQRTVVDVVQEVVHQLCERDRYMQQQIAWIGRCSSDPRVRNALVLATTEEYCLRPVRNQPLLAYRFFNYLRRSQRGGLTQVPEAELIRLVSDEIAPDDADGAVSLLDAEAIAMAEDATLWEEQQLLRLSVQKEFEQYLQQNIDETAAEWLRLYLKGRSQDEIAKLLNLPVRQVYRLREKVSYHAIRVFSLKTEPELVASWLQTSLNEHGLGLTPNQWERYWDRLTPEQRQFLNALKAGNSFEAIARERGMKVSQLVSEWTQLYLMAQSLRNE
>NZ_CP051167.1|WP_168568262.1|1398622_1399738_-|hypothetical-protein
MQSNSETERANPMDTDRIFQLIDNILPFEACLYYEVLPLSINGSRLLLGMVDLEDTAALDYVRRLLGYMKCSLVPKQIDATTHRSVLTSYLNHTHSSAEQKASVSPPKPEAKHPSPPMAGGSSTHRGQSAVVLNRLGQLVNKPSPPPKPPTLPQPPKLPPPHPDAEVPVLEISAAHLDSPLEVLASLPPKQLLQELLGRVLTGGIGRLYFERQAEYGRILWSQDGVVQSVLDRLDLSLFQSVINELKRLTHLPLLPVEKPRQIEIERRYQGADLLLRLRVMPSDHGEDATLQVLRGAALKFYQQQQLVTLSRDALRLAQQLQRKVDELHKQAGNHPKLLEDQPLEALPALDQLLKQVDRQLDVLRHLETKD
>NZ_CP051167.1|WP_168568261.1|1397432_1398494_+|3-deoxy-7-phosphoheptulonate-synthase
MIIVMKSGAPEAEVDRLTEELNQTWGLTPEKIVGRYKVVIGLVGDTADLDPLQLQEMSSWIEQVLRVEQPFKRASREFRHGEASDVIVNTPNGPVHFGENHPLVVIAGPCSVENEEMIVETARRVKAAGAKFLRGGAYKPRTSPYSFQGHGESALELLAAAREETGLGIITELMDTADLEVLGEVADIIQVGARNMQNFALLKKVGAQDKPVFLKRGMSSTIEEWLMAAEYIMAAGNPNVILCERGIRTYDRQYCRNTLDLSVIPVLRSLTHLPIAIDPSHGTGWAEYVPAMAKAAIAAGTDSLMIEVHPNPQKALSDGPQSLTPDRFDRLMEELAVIGKAVNRWPQPEAVLA
>NZ_CP051167.1|WP_168568260.1|1396789_1397245_+|DUF3464-family-protein
MSSEPQRSPIPFEPKNRKKQRRKAATKGSNVGKTGREQAEVARRASPSQRTIPEAVSRRMIRRMVFFCGLPTALGISSFILSYFIVTEQWFPLPNAAVVAVSMGFFGMGVLGLSYSVLSASWDENTPGSWLGWNEFVVNFRRMTQAWRSSR
>NZ_CP051167.1|WP_168568270.1|1411197_1413048_-|DUF3352-domain-containing-protein
MSESKSESKPENQTPQKIPLAVAIAGVGLLVGGGVAALWFLWKQQPSAQLPSGTTLVPNEALMSISLSTDSREWEKLRQFGTPESQAWFDEQLLTLRDRLLSDNGYNYQEDIEPWVGKEITIAFLPPIPVEVSESEGEGETANSDGEGEPEQNGEENAETPSLSGIPRGNQSIVLLLPIANASRAQQVLENAPTPQSGAWTTREYKGVEIKENPGTDSDLYAVTVLDGKFLAVANSRYGIDRTVDTYKGALSLADLPNAGKIWQKLEGDRAFARLFVNIPVASAVASLNRQNARIDEIAKLQPNQGLAATATIENDGIAFDSAMWRRPKSERTYSVENKAKMMADRLPAAMSIAIVGSNLQGLWNDYVAEIDVNPIAVINPQWLRTAIKTTTNLDLEQDLLSWMAGEFALAMIPPAEDNASTFPASVVLMVQASDVKAGEETLAKLDERMQEAYQFKLSRETIGDRELVTWQSPQSSLIVTRGWLDGNVAFLSVGAPLADRIVPKPQTSLRTNTLFQSTVPAQPTPSNGYVFIDVENLLALNAPELRLPTQQGAFLDAIRAIGLRMAVENDRTLRHHLFVRLKQAGEALPLPPAQPDRPPSSESGSPTTPTPENNN
>NZ_CP051167.1|WP_168571763.1|1413622_1415026_+|flagellar-motor-protein-MotA
MSHSPRQELEVSIPLVFTLATVLTGVIYAIFLERRQTYLGTLLYDRGFTQVAVVFFAGIVLSFTILKFVKLQREFFALRENWVAVDLDWHDPQSPLLFRLQERLLADGSAIARRCARAIAAYIHSGNRKAAAELALDDSSFYLSASESSYSLPRILVWAIPLLGFIGTVIGISQAVTGFSGFLEEAGEIDQIKEGIGTVTSGLAVAFDTTLVALFLSVLVMIPLVLVERFESRLLLAIDIYLNDRLLPRFKDSGTPLENEQLTQAIDAAIARHLPSPEALIDPARTYAERAAEVLSQTFIAQLNTVQTQHERLIEKLDNLQEKTLEERQAFELSFSENEENYRQAIADLITEINGTYRKVSAEMEAGNRAIAQNLIQQAEKIGDRLEHASKSLDSRIALLEKSKTNIAQILELQERLDKNLRSISRDGHIEAVLEEIREHLAELKPLLKQLNKPRRITLVETEDKIE
>NZ_CP051167.1|WP_168568271.1|1415044_1415515_+|hypothetical-protein
MYRRRFTRRSIQIELFPFLSVLACTIGTLILLIIVVSTQILGNEREVTIIARGETGTNENKTPRYIECQQDGVIIYPHQTFVPLAEIDRPDSALSRLLDEVEKNRDRQYLIVTMRPQGIEVFKRVREAIERRGIDIGYEPLDEGWRLKIEDEIERL
>NZ_CP051167.1|WP_168568272.1|1415607_1416315_+|hypothetical-protein
MRRRRRIRQSGIPGQNLDSFLDILTNTVGVLMFVGLFISIVAVESGTIVRTPIVSETRKNAHFFEFRNNRLHYLDKEEAEREINQFFQSLPQCYEPYVPPAVDPEIVPYYLDLIEEYRRCLNVKTARVEQFSAETTAYEVRIKLNPTGLIYLPKPEFSGETPQELRSPDSQFKQILKQFDPRTDYLAFIVRPDSFEAFRAARKQAWNDGFDVGWEPLELNSIIVFGSGGRAIGVQ
>NZ_CP051167.1|WP_168568273.1|1416764_1418186_+|pyruvate-kinase
MRKTKIICTLGPASSDYETIKAMVEAGMDVARLNFSHGDHSTHQKNIETLRQISHELDKPIAILQDLQGPKIRVGDMEEGTVLEAGQKTTITMQNVVGNAQKFSSTYKGLATDINEGDTILIDDGLICIQADRVLNNEIYGTVVHGGALKSHKGINLRHSSISTPALTDKDIKDLDFGLSEEVDYVALSFVCEASDIKEVKGAVRRKDKQAHVVAKIERHEAIEDLEQIVMTADAVMVARGDLGVEIPLDRVPMLQKTILQSCRMHLKPAITATQMLESMIHNPRPTRAEVSDIANAILDGTDALMLSGETAVGNYPVEAVRTMARIAETTEARLTTSHQYLNGFEDEGIGNSVVYAACRLAENLKAKAIICFTESGFTGRLLSKYRPMIPAIGVTTDAFVERRLALYWGLQSICLEEVTNTDEMILQVEQAVVKRRFVERGDLVVIIAGLPLPITGVTNLIKVHRIGESYAI
>NZ_CP051167.1|WP_168568274.1|1419020_1419989_-|hypothetical-protein
MDCQQLVPQTFDLSRYQFGAPQVSGRLSVVPIFGGDRPGQFTSPLSGLKLNRVAGYGSVELSNPSREGVAIVPLHIGYVQDQAQNHALCRSAFIAAGQKLMFEDACCVQESQGGYLKGREQWFFILPLQLRSPALEVRHQASYSKLWGKISELNRDFGLSDRGHLEQIITRKRGFLTQYQSRLEYLNGQTGALFFLDDKLAGIEIAPTAAYFQELWMPLVCFCYGVAAFKDEAVREPIAEPFPVKSLAELRESLQDSRQQLQQTLQENLAKTPQQTFEVREEERFLNLRLKTAIGDQFAGQFVEADDELIYASLFAKPEYLN
>NZ_CP051167.1|WP_168568275.1|1420062_1421436_-|VWA-domain-containing-protein
MERNPYTLATVFNHLRSHAEPFVLRDNGQPPEWSDEALHRTLYERQSELYALLALAGGVQTVQRERVLFQLLRASRVGLDDNVRRTLDRVTRILLESLGADRVLRVFLAVRRERANHKHARKAILRYILNHPQFEDLLGSRRPAVADSLEHAIGKNVARACAKWLAEGERSRQTYVRRNLLRFARDPARVESLFPTLYRGGVRSLATGAYQQTHRDRAEPLDREPERPKTVTATNRGDIAATLVHLYRGGSSPELERAVDAYVEAAARPLPYFEGKVAVVLDGSTSTRGYGEREYCTIAQSVAFQRVLQRRCDRLEVFPVGGSGTLPQPQGPSDLATATIAAIESQPDLVAIVSDGYENTYPGDLARVTATFAQLGIQTPVVFCHSKFSPNDDLSLRRNAPNLPQFEFWHQEDFEGVLVALFSFVEGEKGERTIHNFLLKKLEIVEQWLDRPLEKAA
>NZ_CP051167.1|WP_168568276.1|1421610_1424088_-|PAS-domain-S-box-protein
MAKILIVDDDLTVQLVLRDLLESEGHQVSVALNGQEGLQRARAEHPDLMICDWMMPVLDGLQVCRQVKADPQLATMFFILLTAREEVDDRVKGLDTGADDFLSKPVEAEELLARVRAALRLHHLTRELSQANQQLATLVEVQRRLLAFQGDRPARDLERSPYPEVLEPLGKAAGATRVYLFQIPSPSTGDVRAGTRSENCPPLEDRAVCLADWSASETDASGATSSRICDRQWRDRLIQFPPRWLHHLTRGETVAGISRDFPEGERQMLEAAGVRSILMLPLIVNGEFFGFVGFDNAREARPWSESEVSLLKAAAAAISLHQERIGAEAALRKSEARYRAIVEDQTELICRFAPNGRLTFVNDAYCRYFNVEREQLMDGSLVPLIPHEPLDVGETPAVSREHRIVMPDGTIRTQQWTERAIFDERGRLSEFQAVGRDITERKQAEAALRSSEERFRQLAENIEAVFWIGDRHGRELLYVSPAYEQIWGLTCEDLYRNPAARFEAVHPEERDRLWAALHPLDCLDLEYRIVRPDGSIRWIRDRGFPIRDESGEIYRVAGIAEDITERKHAEEQLRQAIAKEREVMELKTRFISMVSHEFRTPLTTILSSADLLEFYIEESAVDRLEKKRQALNRIQNSAVNMTQLLEDVLFIGRSEANGISFQPQSLDLETFCQNLIEELHLVNTQDRKIQFFQNDRRLGPDSPPPRLDSKLLRQILSNLLSNALKYSPPGGRVEFTVDYYDRQIAFTVKDSGIGIKSEDLPRLFELFHRCSNVGDIPGTGLGLAIVKRSVDLHGGEITVDTQVGVGTTFKVTLPLSALPPVPLQQ
>NZ_CP051167.1|WP_168568277.1|1424794_1425241_-|helix-turn-helix-domain-containing-protein
MPAKNFLTAEQKKALQTAIRENSCPRLREHALILLLQNDGKTYEEIAKFLGCSYRTVAYWCVHGDPDNIESLRDRRERGNYRKADENYIQTLLELVNTPPESLGYDCQHWTSQRLASHLSKKTGIELSGTQILRILRKHKIRLPMSRV
>NZ_CP051167.1|WP_168571764.1|1425404_1425896_-|pentapeptide-repeat-containing-protein
MVAIALCSSCGVNQTYVKRLMELKQCQGCNLERVDLSHQILSGANLKGSNLSGGNLQRSTLFSADLNGARLVKTDLQGADLGAANLSKADLRNADLRGADLSSADLSYADLRGSNLEYANLSNANLGNARLSGAKLEGANLAHAELDGAIGLVVDDATGDRQP

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Crispr_ID: NZ_CP051167_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_8

1524104-1524189

Orphan

N:A

Consensus_repeat	Method
TTGCGCGATCGCGATCGCGCCGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051167_8

>merge|NZ_CP051167|8|1524104-1524189|CRISPRCasFinder
TTGCGCGATCGCGATCGCGCCGAATGTAACTTGTCCGAAACTGAATAAAAAGCCGATCCCAAATTGAGCGATCGCGATCGCGCCGA

>NZ_CP051167|8|7|1524104-1524189|CRISPRCasFinder
TTGCGCGATCGCGATCGCGCCGA	ATGTAACTTGTCCGAAACTGAATAAAAAGCCGATCCCAAA
TTGAGCGATCGCGATCGCGCCGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168568358.1\|1520331_1520790_-\|SRPBCC-family-protein	unknown	unknown	gnl\|CDD\|176862
NZ_CP051167.1\|WP_168568359.1\|1521281_1521548_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568356.1\|1519263_1519764_+\|TIGR00725-family-protein	unknown	unknown	gnl\|CDD\|375733
NZ_CP051167.1\|WP_168568372.1\|1535469_1536846_+\|YvcK-family-protein	unknown	unknown	gnl\|CDD\|376670
NZ_CP051167.1\|WP_168568357.1\|1520019_1520229_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568366.1\|1528935_1529229_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568369.1\|1531753_1532173_+\|AbrB-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|372980
NZ_CP051167.1\|WP_168571772.1\|1516077_1517247_+\|4Fe-4S-ferredoxin	unknown	unknown	gnl\|CDD\|372225
NZ_CP051167.1\|WP_168571773.1\|1520954_1521143_-\|CPXCG-motif-containing-cysteine-rich-protein	unknown	unknown	gnl\|CDD\|379524
NZ_CP051167.1\|WP_168568360.1\|1521958_1523590_-\|radical-SAM-protein	unknown	unknown	gnl\|CDD\|188475
NZ_CP051167.1\|WP_168568371.1\|1534149_1534932_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224052
NZ_CP051167.1\|WP_168568361.1\|1523634_1523886_-\|SemiSWEET-transporter	unknown	unknown	gnl\|CDD\|226580
NZ_CP051167.1\|WP_168568370.1\|1532613_1534029_-\|MCE-family-protein	unknown	unknown	gnl\|CDD\|178642
NZ_CP051167.1\|WP_168568367.1\|1529339_1530392_+\|UDP-3-O-(3-hydroxymyristoyl)glucosamine-N-acyltransferase	unknown	unknown	gnl\|CDD\|234858
NZ_CP051167.1\|WP_168568363.1\|1524645_1526208_-\|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|224154
NZ_CP051167.1\|WP_168568365.1\|1528609_1528939_+\|DUF1232-domain-containing-protein	unknown	unknown	gnl\|CDD\|225876
NZ_CP051167.1\|WP_168568364.1\|1526392_1527928_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568355.1\|1517376_1519137_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|226372
NZ_CP051167.1\|WP_168568368.1\|1530659_1530920_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568354.1\|1515343_1515874_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|215180

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168568358.1\|1520331_1520790_-\|SRPBCC-family-protein	gnl\|CDD\|176862	cd07820, SRPBCC_3, Ligand-binding SRPBCC domain of an uncharacterized subfamily of proteins. Uncharacterized group of the SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain superfamily. SRPBCC domains have a deep hydrophobic ligand-binding pocket and they bind diverse ligands. SRPBCC domains include the steroidogenic acute regulatory protein (StAR)-related lipid transfer (START) domains of mammalian STARD1-STARD15, the C-terminal catalytic domains of the alpha oxygenase subunit of Rieske-type non-heme iron aromatic ring-hydroxylating oxygenases (RHOs_alpha_C), Class I and II phosphatidylinositol transfer proteins (PITPs), Bet v 1 (the major pollen allergen of white birch, Betula verrucosa), CoxG, CalC, and related proteins. Other members of the superfamily include PYR/PYL/RCAR plant proteins, the aromatase/cyclase (ARO/CYC) domains of proteins such as Streptomyces glaucescens tetracenomycin, and the SRPBCC domains of Streptococcus mutans Smu.440 and related proteins.	1.97644e-50
NZ_CP051167.1\|WP_168568356.1\|1519263_1519764_+\|TIGR00725-family-protein	gnl\|CDD\|375733	pfam18306, LDcluster4, SLOG cluster4 family. Family in the SLOG superfamily, observed as a standalone domain with little informative genome context, although related families in the SLOG superfamily are predicted to function in diverse conflict contexts.	9.65598e-55
NZ_CP051167.1\|WP_168568372.1\|1535469_1536846_+\|YvcK-family-protein	gnl\|CDD\|376670	pfam01933, UPF0052, Uncharacterized protein family UPF0052.	1.52056e-142
NZ_CP051167.1\|WP_168568369.1\|1531753_1532173_+\|AbrB-family-transcriptional-regulator	gnl\|CDD\|372980	pfam14250, AbrB-like, AbrB-like transcriptional regulator. This family of DNA-binding proteins is likely to act as a transcriptional regulator. This family does not include E.coli AbrB, which belongs to pfam05145.	5.5371e-40
NZ_CP051167.1\|WP_168571772.1\|1516077_1517247_+\|4Fe-4S-ferredoxin	gnl\|CDD\|372225	pfam12617, LdpA_C, Iron-Sulfur binding protein C terminal. This domain family is found in bacteria and eukaryotes, and is typically between 179 and 201 amino acids in length. The family is found in association with pfam00037. LdpA (light-dependent period) plays a role in controlling the redox state in cyanobacteria to modulate its. circadian clock. LdpA is a protein with Iron-Sulfur cluster-binding motifs.	6.76416e-109
NZ_CP051167.1\|WP_168568365.1\|1528609_1528939_+\|DUF1232-domain-containing-protein	gnl\|CDD\|225876	COG3339, COG3339, Uncharacterized conserved protein [Function unknown].	1.83283e-20
NZ_CP051167.1\|WP_168568360.1\|1521958_1523590_-\|radical-SAM-protein	gnl\|CDD\|188475	TIGR03960, radical_SAM_domain_protein, radical SAM family uncharacterized protein. This model describes a radical SAM protein, or protein region, regularly found paired with or fused to a region described by TIGR03936. PSI-BLAST analysis of TIGR03936 suggests a relationship to the tRNA pseudouridine synthase TruA, suggesting that this system may act in RNA modification. [Unknown function, Enzymes of unknown specificity].	4.72639e-98
NZ_CP051167.1\|WP_168571773.1\|1520954_1521143_-\|CPXCG-motif-containing-cysteine-rich-protein	gnl\|CDD\|379524	pfam14255, Cys_rich_CPXG, Cysteine-rich CPXCG. This family of proteins is found in bacteria. Proteins in this family are approximately 60 amino acids in length. There are 5 conserved cysteines which occur in a CPXCG motif and a DCXXCCXP motif.	2.28314e-18
NZ_CP051167.1\|WP_168568371.1\|1534149_1534932_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224052	COG1127, Ttg2A, ABC-type transport system involved in resistance to organic solvents, ATPase component [Secondary metabolites biosynthesis, transport, and catabolism].	1.18995e-119
NZ_CP051167.1\|WP_168568361.1\|1523634_1523886_-\|SemiSWEET-transporter	gnl\|CDD\|226580	COG4095, COG4095, Uncharacterized conserved protein [Function unknown].	3.57202e-18
NZ_CP051167.1\|WP_168568367.1\|1529339_1530392_+\|UDP-3-O-(3-hydroxymyristoyl)glucosamine-N-acyltransferase	gnl\|CDD\|234858	PRK00892, lpxD, UDP-3-O-[3-hydroxymyristoyl] glucosamine N-acyltransferase; Provisional.	8.02811e-151
NZ_CP051167.1\|WP_168568363.1\|1524645_1526208_-\|NAD(P)/FAD-dependent-oxidoreductase	gnl\|CDD\|224154	COG1233, COG1233, Phytoene dehydrogenase and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	7.25203e-83
NZ_CP051167.1\|WP_168568370.1\|1532613_1534029_-\|MCE-family-protein	gnl\|CDD\|178642	PLN03094, PLN03094, Substrate binding subunit of ER-derived-lipid transporter; Provisional.	3.35501e-34
NZ_CP051167.1\|WP_168568355.1\|1517376_1519137_+\|AAA-family-ATPase	gnl\|CDD\|226372	COG3854, SpoIIIAA, ncharacterized protein conserved in bacteria [Function unknown].	5.35306e-117
NZ_CP051167.1\|WP_168568354.1\|1515343_1515874_+\|hypothetical-protein	gnl\|CDD\|215180	PLN02316, PLN02316, synthase/transferase.	0.00146495

>NZ_CP051167.1|WP_168568361.1|1523634_1523886_-|SemiSWEET-transporter
MIVTFLGLLAGTLTTISFLPQVIKTWKSKSAKDVSLEMFLIFCSGVFLWIVYGILVGDTPVIVANFVTFILASTILWLKLKYR
>NZ_CP051167.1|WP_168568360.1|1521958_1523590_-|radical-SAM-protein
MTSTVFDAERLLFTPAIPDADAIELIYAFPNDYSIGITSLGYQIVWSTLASRQDVAVSRLFLDLHEPLPTTPELFGFSVSWELDYVNILGLLESLNIPIRASDRGAGDPLIFGGGPVLTANPEPFADFFDLILLGDGENLLNAFVEAYKTVRSRDRASQLRTLARVPGIYVPSLYQVTYDRPDGAIAAIEPVDPDIPERIAKQTYRGNTLSVSPVVTEKAAWPDIFMVEVVRSCPEMCRFCLASYLTLPFRTASVDASLIPAIERGLTVTRRIGLLGASVTQHPEFSHLLDYLCQPQFDDVRLSIASVRTNTVTEQLARTLAQRGTKSLTIAVESGSDRVRKIINKKLENSEIIDAAINAKAGGLKGLKLYGMAGIPGEEAEDLEATVEMMRSLKKAAPGLQLTLGCSTFVPKAHTPFQWFGVNSEAKKRLKTLQKELGRLKIDFRPESYNWSVIQALISRGDRRVSHLLELVRHYGDSLGSYRRAFKELHGQLPDLDFYVRENWDLNQILPWNHLDGPLPVATLKKHLDEASRYFPASTKVR
>NZ_CP051167.1|WP_168568359.1|1521281_1521548_-|hypothetical-protein
MRVEGYFETKNFFIHLCYDSNNDIWYYGIAKGSEAEAIGPLYTYTEEGTGYVVENGDYTYIVTGLSLSIYEGNKLLQEEPVINSHHRE
>NZ_CP051167.1|WP_168571773.1|1520954_1521143_-|CPXCG-motif-containing-cysteine-rich-protein
MDNTAEYCCAYCGESNATFIDFSAGTHQSYVEDCQVCCQPNILYVRIDEDTLDIEIDSAPES
>NZ_CP051167.1|WP_168568358.1|1520331_1520790_-|SRPBCC-family-protein
MLHFEYSSLINAPVETVWKFHERPDILDILTPPWQPVRVVRRDRGLEVGSISEFLIFLGPFPVRWVARHTACETHRLFVDEQQSGPMEFWMHRHEFSAENGKTRLTDAIEYAIPGGWWSELLLGWWVESRLRDMFRYRHEVTQRECEKLTEI
>NZ_CP051167.1|WP_168568357.1|1520019_1520229_+|hypothetical-protein
MNAEELAREKLAEQRLQQEHQHESMTRRATQEIHQSSQGNTDEEARELLVEQRRHEEHQHETMNARAVK
>NZ_CP051167.1|WP_168568356.1|1519263_1519764_+|TIGR00725-family-protein
MGSKIAIGIMGPGLGATKLDCDRAYRLGAEIARHGWVLISGGRNVGVMDAANRGAKSAGGLTVGILPTDDRWGVSEAVDIAIPTGMGSARNNINVLASDVTIACGMGPGTASEIALALKANKKVIILNDRPESQQFFQSLSPQRAIVVDSVEAAIAQVRAIVDRFE
>NZ_CP051167.1|WP_168568355.1|1517376_1519137_+|AAA-family-ATPase
MQITDDLNQLLDILPESIRTPLEQQEQLGSLVEVVMDLGRIPEARFPEGAKYLSDLPVSRNDLNYCIARVGEFSGDNRAGIEQTLHRISAMRNRQGEIIGLTLRVGRAVFGTIGTIRDLVERGQSILMLGRPGVGKTTALREIARVLADDLHKRVVIIDTSNEIAGDGDIPHPAIGRSRRMQVATPEQQHKVMIEAVENHMPEVIVIDEIGTELEALAARTIAERGVQLVGTAHGNQIENLIKNPTLSDLVGGIQSVTLGDDEARRRGSQKTVLERKAPPTFEVAVEMIERQRWVVHENVAETVDCLLRGRQPTPQIRTISETGKVTITRELPQPQGLPTVAAPPFGATGWRASGQMKALPMQNRGDRPGRRDRELGSEHKSFEQMLEESLYSQSYRGERSRGVDDEFAMGASGPNGEDLPLHVYTYAVSRHQLDRVIRTLSLPVVTTKDIDGADAVLALRSHVKNHSKLRQMAKNRQLPIYTIKASSIPQITHALKRLLHMDGDALEEVTDLSLFSQSGSEDEIEALEEARLAVEQIVLPKGQPVELLPRSPKVRKMQHELVEHYRLKSCSFGDEPNRRLRIYPA
>NZ_CP051167.1|WP_168571772.1|1516077_1517247_+|4Fe-4S-ferredoxin
MHVNSPLKALSQGHWFKLICGASFGHLPAVRNLALAYTLVGADCIDVAADPAVIAAAKQGIEAALEVAAARGDRLGIGGNLRRPLLMASLNDGEDPHFRKAEFNPAICPSDCPRPCERICPARAIRFESSRSGVIDELCYGCGRCLPVCPIGQIVTRSYVVAPGTIAQLILDSGIDAIEIHTQVGRLEDFKRLWGAIAPKVNRLQVLAISCPDAEGSIDYLRSLYAAIAPLPCPLIWQTDGRPMSGDIGAGTTHAAVKFARKVLAADLPGYVQLAGGTNHHTVAKLQQEGLLRTTSGADKQAIAGIAYGSYARALLAPVLDQLEIADGTQTPEVMPLEQQPDLLREAVNLADSLVSPLKIPIQLQNTTNNYTPAIDATMTRKPSAPLES
>NZ_CP051167.1|WP_168568354.1|1515343_1515874_+|hypothetical-protein
MTDEIDKLLAKVKSEYDPSGPPATPESTPTPPKQEAKAASTPQNTGSIDNLLAQIEVEGKTSGRAPTGWQGSPSQSRSPQGSGSFDELLTGVKEEFEGRDRLEREEHERAERERAEEERRRREQQRQKVAKKAQEWLKQLDPYSDEGFWFGQFAEGYASRLEAAIDYLEALEQKSE
>NZ_CP051167.1|WP_168568363.1|1524645_1526208_-|NAD(P)/FAD-dependent-oxidoreductase
METFDYIIFGAGLGGLSAAACLTRQGYRVAVLEKHYLPGGCCHTFDYGNYSFCADVHYIYQCGPGQTVDLFFNYIDRPIAFNSLDPDCIDRIITPDADFRIPLGWENLRRRLLAEFPEEATAIHRYCDEIAQFNAEVRRLGREVHWYDRHLADWLKLPKYWHLFRRRHWTLQDLYDRCGLSPKLQAILAGQSGDYALPPAEIALLSHTAVVWNYSEGAYYPKAHFKAFVDTIVEAIDEGGSAVLLSNPVEHIDVRDGEVKGAIAAGIRYEASRGYISDLDPKLTVSLMHDGTGLRDRERHRLTDYEYSASAFNIYLGLDKRFDPKAYGIGNWNIWYYPTGNLNRAYQKQLEGDLEYPWIFLSSPTCKSDEPGMAPEGHHVLEIATVCPYEPFKKLHESDRKAYRSLKREFYQKIMQSVRDLIPDVDRYARLKVYGTPTTSEYYLGQPQGNIYGAKLIPQQVGLNRLGYTTQLPNLFFVGASSGYPSVPGVIKNGMNLVSLLTGISIGKQSRDRAEELVKI
>NZ_CP051167.1|WP_168568364.1|1526392_1527928_-|hypothetical-protein
MLLPFRKMAIATIALFSLSIPSDRAIATSIGDLLPDWSPEKAVTTNIKDARAISAWLDDFPETVPDPADASLAFAPGYYRFTVQSYCLHAGTYAPTQGDGYLLATLEGNRAELIRAILQRSLAQAQISQQDIQRLIWGIEAGANFTQYPLDFQVRIAPLLEPSEIAALSIDVESIAGRLIGRFIPDSLKRALNLYRDIRQTLTNAQATYEDLERIAILTGVAPTGKGSRTIDPGNWNYAGDGFYLRTYPQSYPTTTVELLRPAAYRLQRDARGRIIVFESGNYRIETTYEDTPGGDRLVSPEGESVPIWRFRRLHFSGPQPGDEWTVENTGWIVASSEGTDYGDRPGAKLAAIAVKTTSGDRARPQILASGGNGEPTWKTYRDRVNSAREKWEKLDRYRQELERANRPPSEDAIRDLTDLTHYRDGLEAAKNPADLEGKGEWFRDHLGRVTNGWNYVNCVLAGECDPPGDEFDRDRGDRPKPFDPSGKVAVPGNTVKQRLGLSGRLQSLPR
>NZ_CP051167.1|WP_168568365.1|1528609_1528939_+|DUF1232-domain-containing-protein
MSYSIQSIYNWYRNTLRNPKYRWWIILGTLAYVLSPFDISPDFLPIVGQIDDIAVISLLVAEVSQMTMDYFKSRQGDRDRQGSDFAVNSENATTTVDVEASGTPVSELD
>NZ_CP051167.1|WP_168568366.1|1528935_1529229_-|hypothetical-protein
MLANPIVKDKRGSAIAVESDRNSAIVSSIGGSKNCNFYPAIAHFRSTIALQRTAPGDRLPGDRKSSPQCGLAIKKQPNSLGLESGCLGEGNPWGDRD
>NZ_CP051167.1|WP_168568367.1|1529339_1530392_+|UDP-3-O-(3-hydroxymyristoyl)glucosamine-N-acyltransferase
MKFSELIAQLGDLVLDSRLDTTQGDPEICGVAAIDDAMTASLSYVESAKFAPQIATTQASALILPQDEGIQARANERAIPWLSTREPRLAFARAIALFYKPFHPESEIHPSATVDPEAEIGEGVYIGPHVTVGAGVKIGNRACLHANTVIYPDVEIGDRVILHANCTIHERTHIGADCVIHSGVVIGGEGFGFVATANGWIKMEQSGCTILEDGVEVGSNSTIDRPAVGETRIGRQTKIDNLVQIGHGCQIGENCAIAAQVGLAGGVRVGDRVILAGQVGVSNQVRIGDGAIASAKSGIHSDIAPGEIVSGYPAINNKLWLKAVAIYNRLPEIYRSLKDVQRQLGKNSNN
>NZ_CP051167.1|WP_168568368.1|1530659_1530920_+|hypothetical-protein
MEIVKSIGDRGRPFNVESQTFEWVCSDRNWAGGDTPEASLCERAIAIFSWQEPPSFVLDFEAPGIGRSARRLEIEPPPGSIDLSSI
>NZ_CP051167.1|WP_168568369.1|1531753_1532173_+|AbrB-family-transcriptional-regulator
MSETATSPLTGKALLQKIKELSHLPRRETAKRCGYYTTTRNNQTRVNLTDFYDAVLAARGIPLSPEGTKDGRGREPTYRVSVHKNGQIVIGSTYTHAMGLKPGDEFEIKLGYKHIHLIQVGADKNGSDLDDDELLEDEE
>NZ_CP051167.1|WP_168568370.1|1532613_1534029_-|MCE-family-protein
MRSRTLREGSVGLLILGALGLFGGIVLWLKGVTLGPQSYRILVEFANVVGMQEGASVRYRGVKVGRISSIQPGTNGVEVELTISPPDLVMPSEVLIEANQGGLIGETVVDITPLKPVPTRSANAPKPLDPQCNSDEIVCARDRLKGQIGVSFDELVRGSIRFTRLFSDPAFFNNLNSLVKNTTAASAEVTQLTRQINVLSQSVQKELTAVSSSTNQSALAIATAARQIGNAAGEFGSIADEIGTSVGEIGGAARQFGAIADDIGTSANRLNLTTVEVYRLVSNVNSLVASNRGTLVSTLNNLNQTSEQVRRTISAIAPTLANVEGQIGGGNFGTLFDNLNTLANNAAEVSANAAEASAALREFSSAVGTPTNLLLLQQTLDSARATFQNAQKITSDLDELTGDPTLRENIRNLIESLSDLLSSTQHLEQQTLLAQSLGTLSSTVHSATAHDPSALPSVSVEAIEPSLSQSP
>NZ_CP051167.1|WP_168568371.1|1534149_1534932_-|ATP-binding-cassette-domain-containing-protein
MTEPLIQLKGISKAFGNNVILDRVDLSIYPCEALSIIGPSGTGKSTILRIIAGLLAPDEGEVYIQGERRKGWVDDLADPIGIGMVFQNAALFDSLTVDENVGFLLYQHSKLPRRRIRQLVSEKLEMVGLPGIGNLYPAELSGGMRKRVSFARAIMANPEDPKASPEVLLYDEPTAGLDPIASTVIEDLIRDLQAAQGGCSTYVMVTHQQSTIRRTSDRIIFLYGGKIQWEGSVADSESTDHQAVQQFFSGNIDGPIQAFG
>NZ_CP051167.1|WP_168568372.1|1535469_1536846_+|YvcK-family-protein
MFIALLKQALFAFKRDAPGRRTRMNQWFKWLAPGLFVKRWVLISAGGVFLALLGLSIWIKLTPIYYGIQLIETFLATITSLVPSYISGPLVMLGGIVLILWGQTRTVGSITEVLRPGSDRELVDVLIDHRRLSRGPRIVAIGGGTGLSTLLRGLKQYSANITAIVTVADDGGSSGRLRRENRVLPPGDIRNCLAALAAEEKLLTELFQYRFRAGEGLTGHSFGNLFLTAMMDITGDLERAAAASSQVLAIRGQVLPATLCDVHLWAELADGRKIEGESRISEAGGNIVKIGCIPGNPPALPKAVQAIREADLIIMGPGSLYTSVIPNLLVPEIAEAIACRDVPKIYVCNIMTQPGETQGYTVSDHVKAIDRACGRPLFDSVLAQSQVPSAQALIRYAQDNSHPVFLDREDLANLGRQVVVANVMDEDPQTGYVRHNSQFLGRVLLRWYARVQGIASKE

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Crispr_ID: NZ_CP051167_10

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_10

2027345-2027507

TypeV

N:A

Consensus_repeat	Method
GGGGAAGGGGTTTATACTTTTGCCA	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP051167_10

>merge|NZ_CP051167|10|2027345-2027507|CRISPRCasFinder
GGGGAAGGGGTTTATACTTTTGCCAATGGTAGTGTTTACGAAGGGGAATTTCAAGACGGTAAATTTCACGGGGAAGGGGTTTATACTTTTGCCAGTGGCAACCGCTATCAAGGCGAGTTCGATCGCGGCAATTTAGAAGGAGAAGGAACCTATATTTTTGCCA

>NZ_CP051167|10|9|2027345-2027507|CRISPRCasFinder
GGGGAAGGGGTTTATACTTTTGCCA	ATGGTAGTGTTTACGAAGGGGAATTTCAAGACGGTAAATTTCAC
GGGGAAGGGGTTTATACTTTTGCCA	GTGGCAACCGCTATCAAGGCGAGTTCGATCGCGGCAATTTAGAA
GGAGAAGGAACCTATATTTTTGCCA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168568709.1\|2023423_2023828_-\|biopolymer-transporter-ExbD	unknown	unknown	gnl\|CDD\|223917
NZ_CP051167.1\|WP_168571803.1\|2014829_2016143_+\|lysine-N(6)-hydroxylase/L-ornithine-N(5)-oxygenase-family-protein	unknown	unknown	gnl\|CDD\|226017
NZ_CP051167.1\|WP_168568711.1\|2024888_2026394_+\|TonB-family-protein	unknown	unknown	gnl\|CDD\|367555
NZ_CP051167.1\|WP_168568706.1\|2017380_2019216_+\|IucA/IucC-family-siderophore-biosynthesis-protein	unknown	unknown	gnl\|CDD\|226715
NZ_CP051167.1\|WP_168568719.1\|2040350_2040491_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568718.1\|2040139_2040304_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568710.1\|2023811_2024459_-\|MotA/TolQ/ExbB-proton-channel-family-protein	unknown	unknown	gnl\|CDD\|223881
NZ_CP051167.1\|WP_168571805.1\|2030363_2034191_+\|CHAT-domain-containing-protein	unknown	unknown	gnl\|CDD\|378942
NZ_CP051167.1\|WP_168568704.1\|2014215_2014821_+\|acetyltransferase	unknown	unknown	gnl\|CDD\|379237
NZ_CP051167.1\|WP_043468426.1\|2029270_2029465_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568715.1\|2035703_2036729_+\|hydrogenase-expression/formation-protein-HypE	unknown	unknown	gnl\|CDD\|100033
NZ_CP051167.1\|WP_168568705.1\|2016142_2017339_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|340883
NZ_CP051167.1\|WP_168568716.1\|2036889_2038335_-\|DEAD/DEAH-box-helicase	unknown	unknown	gnl\|CDD\|223587
NZ_CP051167.1\|WP_168568714.1\|2034187_2035570_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571804.1\|2021267_2023223_+\|iron-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|236720
NZ_CP051167.1\|WP_168568720.1\|2040812_2041955_+\|HlyC/CorC-family-transporter	unknown	unknown	gnl\|CDD\|224173
NZ_CP051167.1\|WP_168568707.1\|2019339_2020134_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224045
NZ_CP051167.1\|WP_168568713.1\|2028801_2029251_+\|type-II-toxin-antitoxin-system-VapC-family-toxin	unknown	unknown	gnl\|CDD\|350222
NZ_CP051167.1\|WP_168568708.1\|2020171_2021104_+\|iron-siderophore-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|238566
NZ_CP051167.1\|WP_168568717.1\|2038644_2040000_-\|30S-ribosomal-protein-S12-methylthiotransferase-RimO	unknown	unknown	gnl\|CDD\|273453

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168568709.1\|2023423_2023828_-\|biopolymer-transporter-ExbD	gnl\|CDD\|223917	COG0848, ExbD, Biopolymer transport protein [Intracellular trafficking and secretion].	1.47856e-29
NZ_CP051167.1\|WP_168571803.1\|2014829_2016143_+\|lysine-N(6)-hydroxylase/L-ornithine-N(5)-oxygenase-family-protein	gnl\|CDD\|226017	COG3486, IucD, Lysine/ornithine N-monooxygenase [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP051167.1\|WP_168568711.1\|2024888_2026394_+\|TonB-family-protein	gnl\|CDD\|367555	pfam03544, TonB_C, Gram-negative bacterial TonB protein C-terminal. The TonB_C domain is the well-characterized C-terminal region of the TonB receptor molecule. This protein is bound to an inner membrane-bound protein ExbB via a globular domain and has a flexible middle region that is likely to help in positioning the C-terminal domain into the iron-transporter barrel in the outer membrane. TonB_C interacts with the N-terminal TonB box of the outer membrane transporter that binds the Fe3+-siderophore complex. The barrel of the transporter, consisting of 22 beta-sheets and an inside plug, binds the iron complex in the barrel entrance.	1.55651e-16
NZ_CP051167.1\|WP_168568706.1\|2017380_2019216_+\|IucA/IucC-family-siderophore-biosynthesis-protein	gnl\|CDD\|226715	COG4264, RhbC, Siderophore synthetase component [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP051167.1\|WP_168568710.1\|2023811_2024459_-\|MotA/TolQ/ExbB-proton-channel-family-protein	gnl\|CDD\|223881	COG0811, TolQ, Biopolymer transport proteins [Intracellular trafficking and secretion].	7.30879e-49
NZ_CP051167.1\|WP_168571805.1\|2030363_2034191_+\|CHAT-domain-containing-protein	gnl\|CDD\|378942	pfam12770, CHAT, CHAT domain. These proteins appear to be related to peptidases in peptidase clan CD that includes the caspases. This domain has been termed the CHAT domain for Caspase HetF Associated with Tprs. This family has been identified as a sister group to the separins.	4.48814e-45
NZ_CP051167.1\|WP_168568704.1\|2014215_2014821_+\|acetyltransferase	gnl\|CDD\|379237	pfam13523, Acetyltransf_8, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.55332e-67
NZ_CP051167.1\|WP_168568720.1\|2040812_2041955_+\|HlyC/CorC-family-transporter	gnl\|CDD\|224173	COG1253, TlyC, Hemolysins and related proteins containing CBS domains [General function prediction only].	6.91918e-84
NZ_CP051167.1\|WP_168568715.1\|2035703_2036729_+\|hydrogenase-expression/formation-protein-HypE	gnl\|CDD\|100033	cd02197, HypE, HypE (Hydrogenase expression/formation protein). HypE is involved in Ni-Fe hydrogenase biosynthesis. HypE dehydrates its own carbamoyl moiety in an ATP-dependent process to yield the enzyme thiocyanate. The N-terminal domain of HypE is related to the ATP-binding domains of the AIR synthases, selenophosphate synthetase (SelD), and FGAM synthase and is thought to bind ATP.	5.30151e-169
NZ_CP051167.1\|WP_168568705.1\|2016142_2017339_+\|MFS-transporter	gnl\|CDD\|340883	cd17325, MFS_MdtG_SLC18_like, bacterial MdtG-like and eukaryotic solute carrier 18 (SLC18) family of the Major Facilitator Superfamily of transporters. This family is composed of eukaryotic solute carrier 18 (SLC18) family transporters and related bacterial multidrug resistance (MDR) transporters including several proteins from Escherichia coli such as multidrug resistance protein MdtG, from Bacillus subtilis such as multidrug resistance proteins 1 (Bmr1) and 2 (Bmr2), and from Staphylococcus aureus such as quinolone resistance protein NorA. The family also includes Escherichia coli arabinose efflux transporters YfcJ and YhhS. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. The SLC18 transporter family includes vesicular monoamine transporters (VAT1 and VAT2), vesicular acetylcholine transporter (VAChT), and SLC18B1, which is proposed to be a vesicular polyamine transporter (VPAT). The MdtG/SLC18 family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.75131e-15
NZ_CP051167.1\|WP_168568716.1\|2036889_2038335_-\|DEAD/DEAH-box-helicase	gnl\|CDD\|223587	COG0513, SrmB, Superfamily II DNA and RNA helicases [DNA replication, recombination, and repair / Transcription / Translation, ribosomal structure and biogenesis].	6.98807e-160
NZ_CP051167.1\|WP_168571804.1\|2021267_2023223_+\|iron-ABC-transporter-permease	gnl\|CDD\|236720	PRK10577, PRK10577, Fe(3+)-hydroxamate ABC transporter permease FhuB.	0
NZ_CP051167.1\|WP_168568707.1\|2019339_2020134_+\|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].	1.88463e-121
NZ_CP051167.1\|WP_168568713.1\|2028801_2029251_+\|type-II-toxin-antitoxin-system-VapC-family-toxin	gnl\|CDD\|350222	cd09874, PIN_MT3492-like, VapC-like PIN domain of the hypothetical protein MT3492 of Mycobacterium tuberculosis CDC1551 and other uncharacterized, annotated PilT protein domain proteins. Virulence associated protein C (VapC)-like PIN (PilT N terminus) domain of Mycobacterium tuberculosis CDC1551, hypothetical protein MT3492, and similar bacterial and archaeal proteins are included in this subfamily. They are PIN domain homologs of the Mycobacterium tuberculosis VapC and Neisseria gonorrhoeae FitB toxins of the prokaryotic toxin/antitoxin operons, VapBC and FitAB, respectively, which are believed to be involved in growth inhibition by regulating translation. These toxins are nearly always co-expressed with an antitoxin, a cognate protein inhibitor, forming an inert protein complex. Disassociation of the protein complex activates the ribonuclease activity of the toxin by an, as yet undefined mechanism. The PIN domain belongs to a large nuclease superfamily. The structural properties of the PIN (PilT N terminus) domain indicate its active center, consisting of three highly conserved catalytic residues which coordinate metal ions, in some members, additional metal coordinating residues can be found. Some members of the superfamily lack several of these key catalytic residues. The PIN active site is geometrically similar in the active center of structure-specific 5' nucleases, PIN-domain ribonucleases of eukaryotic rRNA editing proteins, and bacterial toxins of toxin-antitoxin (TA) operons.	0.00024842
NZ_CP051167.1\|WP_168568708.1\|2020171_2021104_+\|iron-siderophore-ABC-transporter-substrate-binding-protein	gnl\|CDD\|238566	cd01146, FhuD, Fe3+-siderophore binding domain FhuD. These proteins have been shown to function as initial receptors in ABC transport of Fe3+-siderophores in many eubacterial species. They belong to the TroA-like superfamily of helical backbone metal receptor proteins that share a distinct fold and ligand binding mechanism. A typical TroA-like protein is comprised of two globular subdomains connected by a long alpha helix and binds its specific ligands in the cleft between these domains.	3.78231e-77
NZ_CP051167.1\|WP_168568717.1\|2038644_2040000_-\|30S-ribosomal-protein-S12-methylthiotransferase-RimO	gnl\|CDD\|273453	TIGR01125, Ribosomal_protein_S12_methylthiotransferase_RimO, ribosomal protein S12 methylthiotransferase RimO. Members of this protein are the methylthiotransferase RimO, which modifies a conserved Asp residue in ribosomal protein S12. This clade of radical SAM family proteins is closely related to the tRNA modification bifunctional enzyme MiaB (see TIGR01574), and it catalyzes the same two types of reactions: a radical-mechanism sulfur insertion, and a methylation of the inserted sulfur. This clade spans alpha and gamma proteobacteria, cyano bacteria, Deinococcus, Porphyromonas, Aquifex, Helicobacter, Campylobacter, Thermotoga, Chlamydia, Streptococcus coelicolor and Clostridium, but does not include most other gram positive bacteria, archaea or eukaryotes. [Protein synthesis, Ribosomal proteins: synthesis and modification].	0

>NZ_CP051167.1|WP_168568711.1|2024888_2026394_+|TonB-family-protein
MSVYGVYSSQRERQEKQIERFIGWSLLGSIALHVAILPLGLQLLAQEPRTVTEEAIEFIVVEKPEVEEPEVEEPTVEEPEIEEPPIEEPPIEESYRSPTETISESSPRESFSEPESIPESPTEPTRPLFDTQNNVDNFDRADSPEIARSISEPQEPQEPQEPREIAPPVTQSPAITDSSEKPAISEPEMPESEISETPSSSFDEPTSPPISEPELSSPPNDPIASPAIEDPTEAIEEFTTTEPPEIARNYENPDIESDFDPGSTEAEFSEPEIASESSAPAVQPPMYNDPSPSDTWDASEPNDPIASSYNDYSTSSRDETGSMAPLDESNPYAESEIGSNAPISSSYSAPIADSTGDSSNFLNETPSYDDSSSSYDSYDAPSNDWDPGASSGFDEPAIANSGPMGDLPNSSSSGSGSGSVGCINCGKPSYPDIAREQGWEGEVLLSVDVDPNGNVSNVQLISSSGYPVLDNTAIDRAWSWQFDSSENGQQGRMVSVPFELR
>NZ_CP051167.1|WP_168568710.1|2023811_2024459_-|MotA/TolQ/ExbB-proton-channel-family-protein
MLDIIAAGGLVAWPLLIASVVAVALVAERSYFWFRIRKRGRKVAKDALQTYLQDPQAAFSKLGMNTDLPIARIFLEALELNDPNPEEFRLALESAVQAEIPVLKRFNTVFETIVNVAPLLGLLGTILGLMNAFSSLQLGDVGGTDTVGVTGGISEALVSTVMGLIVAIFTLLFTNMFRSFYLRELALIQEAGGQLELFYRHRYEREQEKTYASTR
>NZ_CP051167.1|WP_168568709.1|2023423_2023828_-|biopolymer-transporter-ExbD
MRVPDEPENSPQINIVPMIDIIFSILAYFIISSLFLSKSEGLPVNLPKASTAQVQAETRKMTITLDAEGVISLDKEEIELDSLEENLRDRIEKEGESLVILNADEALDHGRVVAVMDKVRRIEGAKLAIAAKKQ
>NZ_CP051167.1|WP_168571804.1|2021267_2023223_+|iron-ABC-transporter-permease
MLLAIAHLAQGEIEIDLLTVLGAVFAPDGSPNAQIVRSLRLPRSAIAVMTGAAWGMAGVLFQTVTRNPLSSAATLGINAGAYFSVTAALIFVPQWFDRSPVGVALAGGILAAALVYAIAAGVHLSPLRLTLSGVAVSLALASLTAILQVFYENQLSGIFLWGAGSLRQTDWSNAAYAAPRIAIPATFALLLSKNWDILLLGDDVARSLGQNLQKTRMICTAIAVFLAALSVSVVGPIGFIGIVAPHLVRLMGCRSHWTLLPAAAIWGAIVLVGADICALQFSAGFGEIPVGTTIPLVGAPFLIWLVGKNERLDRGSSPARSSSHQGRSYPYPALTLAAIGLIFVAAIASLSLGTLSSSPGKFLALIAGNASELYTWVVFELRLPRLVVSLLAGSSLAVSGLLLQSVVRNPIAGPEIVGITSGAGLGVCFILVLFPGASVEAVAIAAFVGAFAVFALIGAIAWRSNLSPTRLALVGIAVSAFCTAGINLLVVVAQLRVARALVWLAGSTYARNWEDIARLSPWPLVLLPLAWVFAPWLDLMALGEDLPRLLGVQLQKARALAISIAVALAAAAVSTVGTISFVGLVAPHIARLLVGSRHRQLVPLAALFGALLVAVADTLGRIVVAPAEIPSGLVTAAIGTPYFLWLLWRSR
>NZ_CP051167.1|WP_168568708.1|2020171_2021104_+|iron-siderophore-ABC-transporter-substrate-binding-protein
MLKKPSKFLKLLVCFLLGVFIFSCTSDRPQLNLKVNGEYPKRIVALEWVYVEDLLTLGIQPVGVADITGYQQFVQIEPQLAEDVVDVGTRQEPNLEAIAELDPDLIIGVQFRHEYIKETLSKIAPTLLFNPYPPPPPQGIRQLDEMQATFLKIAETVGQAERGKAVLKQMHSNFDRISQQLKGIGLDDAKFVLGQLPPIGPELRLFNESSMAVQILQEIGLNNLWKGNSNSFGFNSVWVESLPQIETAHFFYISNKSNPYLELLTNNFVWKNLKFVKEDRVYSLDGQTWLFGGPLSAELLGKNVIKNLVK
>NZ_CP051167.1|WP_168568707.1|2019339_2020134_+|ABC-transporter-ATP-binding-protein
MIAATDWAIRAINLKISYDDLAIVSDLSIDIEMGKITALIGPNGSGKSTVLRTIARLLKPERGLIYLNGKNIAKMPTQAIARELAMLPQSPDIPAGITVWELIGYGRYPHRSLLGTLSRQDKIAMEWALEMTRLQSLRDRAVDTLSGGERQRAWIALALAQKTGILLLDEPTTFLDIRHQLDILSLVKSLNREQQITVVWVLHELNQAAAYSDRMIMFRSGEIMSMGTPAQVMTPEKILEVFGVKMTVIPHPVNGLPTCFPINY
>NZ_CP051167.1|WP_168568706.1|2017380_2019216_+|IucA/IucC-family-siderophore-biosynthesis-protein
MKNLDTLNATLQSQRWQNVSQKLLAKMLSEFMYEEIVKPECLQQTGDRQALYKLSLPEGIAYQFEAKQRLFDSYRVKPDSIQRWDGQIWQQGSSPFQFVLDCHTAVGMTVETAGHLIKELSQTLLADAHIDRQKSEQQSEQQTDLLALDYAHLEGKMEGHPWITFNKGRIGFGYADYLAHAPENQQPVHLPWLAVSKKTAQFNAIADLDYEQAIAEELSASDLAQFKAILTAQNRNPDNYLLMPVHDWQWDNKIIPIFAEEIAKGKIVYLGKSSDLYLPQQSIRTFVNISNPHKRHVKLPLSILNTLVYRGLPGERTAIAPKVTEWITSIWKNDSFLSQKCRLILPGEVASINYEHPYFTALHGAPYQYKEMLGCLWRESVLSYCETDEKLITLAALVHIDGNGKPFVSQLIEKSGLSPQVWLDRLFNTVLPPLLHYLYRYGVVFSPHGENTILVLKDYIPHRLAMKDFVDDVNVSRHPLPELESIPADLKGILLSEPPEGLCQFIFAGLFICHHRYLSDILEEFHQYDERDFWQQVRQVILNYQRQFPELQDRFELFNLLAPKFTKLCLNRNRLITYGYADDGDRPHAAAFGKVNNALHEAISDRLNLSV
>NZ_CP051167.1|WP_168568705.1|2016142_2017339_+|MFS-transporter
MKVNPKWIPIALFSCVFISIFTEVLLSPFYPQFFSKVFGIEDLSYTGYYIFICRLTVVLCAPLWGVFSRWIEVKYLLYCAQIGTAFFTALMATSTSANCFLAYTIGLLLFKSCYLMVYPLIIQLTDSQQHSTVTGTYQAVFHGGIIAATIAGAWMVNLEAPLSLFYAIAIADLFQFLLCFIFLRDTQTRREITPPSEQHSSFGDRWGFIVAIGLIILTFQLANNLIRPFFTAYVTQSETLGITLNESSYLFMIPSAMAIAALPYIRKSFHRDRLHSIYLVGLVLLSVTLFLQGWTISLGILIIARLIYGFCLATSQSALELRLFDRSRGDRLHFNYSLAMSFANLGHLSAPLLASWLVERYTLAMPLFVAAFICAVNFLFAQKTIFRAPIFQPSEVEL
>NZ_CP051167.1|WP_168571803.1|2014829_2016143_+|lysine-N(6)-hydroxylase/L-ornithine-N(5)-oxygenase-family-protein
MNGKIYDLIGVGLGPFNLGLAALLDQTNLDCLFLEQKPEFQWHPGLLIENSTIQVPFLADLVTMADPCSPYSFLNYLHAQSRLYHFYFFEKFHIPRREYNHYCRWVSQQLNSCQFGQRVESLTLENIDFETYYKIESRELKTGKMNTYFAHHLVLGVGSIPQVPPCFQNIYSDHIFHSAEFLNRRDRALQSDSITVIGSGQSAAEVFYELLQQQSNYSYRLEWHTRSAGFLPMEYSKLGLEHFSPDYIDYFYHLPPQKRDRLLSEQRLLYKGISFETIADIYDLLYERSIGGQPLNVRLLPLVEVKEVERVTTEKGDRFVLGYRHSQQETRFTHETDCVILATGYRHAIPRCIDGIRDLIQWDSRGRYEVKFDYRLALNREISNHIFVQNGELHTHGIGAPDLGLGAHRNSVIINTLLGETVYPVERRNVFQQFGVA
>NZ_CP051167.1|WP_168568704.1|2014215_2014821_+|acetyltransferase
MKFPQTEEKLQFSYKKFDRSLEKTIAFRPVELEKDLDRIHRWMNEPHVIPFWQLNFDRDRMRSHLEKALSDRHQTLYIGYLDGVPMSYWEAYWAKDDAIAQCYEPDAGDRGIHLLIGEPKFLGKGYALPLLRAMTNLQFEFSATPKLQTQKVVTEPDIRNAKMIHIFKRCGFVFQREIELPDKRAALMFCDRQSFRKKSEQ
>NZ_CP051167.1|WP_168568713.1|2028801_2029251_+|type-II-toxin-antitoxin-system-VapC-family-toxin
MVAVYLDVCCLNRPFDDWAQERVRLEGDSVLTILERVRTGEWQLISSEAILVELEKMRNLEKKTSILSLLALATQMQEINPTVEERSQQLEGFGFGLFDSFHLACAEAAGADIFLSTDDRLLKTARRYASQLKVAISNPVVWLIQVLQE
>NZ_CP051167.1|WP_043468426.1|2029270_2029465_+|hypothetical-protein
MNAVELREKGYQILVNHLGQSDAIRFLQQMGWGQGDYTQERRDVLESVTREEFLEDLRKIRGLQ
>NZ_CP051167.1|WP_168571805.1|2030363_2034191_+|CHAT-domain-containing-protein
MRQNMESIVPALGDTIAQWIQGVLTQQPDQAEGVAGLVENTCISIQEFPYGRYAEVQEIAIRGYDLVLALRANQPEKRAQTLTNLGVAYLTQAQFGLDPAANLDQAIAAYTEAAAIRRRPGLEKDLASTLNNLGNAYQTQAQFGLDPAANLDQAIAAYTEAAAIRRRPGLEKDLASTLNNLGNAYQTQAQFGLDPAANLDQAIAAYTEAAAIMRRPGLEKDLASTLTNLGVAYLTQAEFGLDPAANLDQAIAAYTEAAAIRRRPGLEKDLASTLNNLGNAYQTQAQFGLDPAANLDQAIAAYTEAAAIRRRPGLEKDLASTLTNLGVAYLTQAEFGLDPAANLDQAIAAYTEAAAIRRRPGLEKDLASTLTNLGVAYLTQAEFGLDPAANLDQAIAAYTEAAAIRRRPGLEKDLASTLNNLGNAYQTQAQFGLDPAANLDQAIAAYTEAAAIRRRPGLEKDLASTLTNLGVAYLTQAEFGLDPAANLDQAIAAYTEAAAIMRRPGLEKDLASTLTNLGVAYRTQAEFGLDPAANLDQAIAAYTEAAAIMRRPGLEKDLASTLTNLGVAYLTQAEFGLDPAANLDQAIAAYTEAAAIMRRPGLEKDLASTLNNWGFTYQQQSQYYSSDPERKQTALENAYRTFAEALEQVEYLRGEITTEDYKRNFNEQWNKIYRGMVEVCLELGNYTAAIEYADRSKARNLVELIATRDAYPQGISPEDRQRLQQLRQAIFQEDRRLQQDPNRDSSHLNQLRDEFQKKFPYQPLHFPQIQQLLDEETAILEWYILGDKFLTFTLTAQTLHLWTSSPEDLEKLGEWGNAYLNDYRRNKTQWQDNLQQRLDSLTQILHLDEILQNLRENFPNCQKLILIPHRYLHLFPIHALPVLTGENQSQTLQELFPKGVNYAPSCQLLQQAQNRPRRHFTHFFAVQNPTEDLTFADVEVETIRSLFPQRRSLQRNNATKATFLAKDLSQTHHLFFSCNAEFNPNSPLDSGLQLADGILTLEEIIASLNLSECSLVTLSACESGQVALDQTDEYISLSSGFILAGSPSILVSLWFVDEVSTALLLIKTYETLQQHPGQLAIALKTAQIWLRDTTVAGFQDWVQKCPLLGDWRDALAEFFQNLGQNEKGINDRPYKSPYHWAAFCVVGQGEQNMASDRDKIQAFIKLIQENPDNLFADHWSSLTELPNQFTDDDEKNVELIEQWVKEPTRTDIYQVYQDRYRSANPLLGATGHKGGFGSQQTPKEAGKSSGELIDQAIKHNTTRPDSPRQSPQNES
>NZ_CP051167.1|WP_168568714.1|2034187_2035570_+|hypothetical-protein
MKNFSLSLYAFHLRQALDDPPDSVNPEADRLWESLTQLSKVLDFPELKNLKSQLICYSPDSDNRPQYHPQAENTLRYEWLSHHAGEVKFTAIPTPAGFKLGGKLQPFRLHDTYCVDLTLSPDPQDLELGVENLGCFHPKDLVSQIEANLGKFVWLTGYSTESELPKQAEAWVNAFCAKTGLIPEFIEGGKLFHADCFLYEAQNITILISIANPNNSTEVEQSANDNYDRFRNLLWSRQKILFVQEKAKQCYENTRKIYSQLENQINSFYELFESPTEARLKKLDSLLTSLPKDLLEYNCYLRDLKAHYTTLDTNAQNFKTCLDRVIQPGDNLQTWADFAEKICPRFLTQIKTYINYLEPGKELFTELVNTIRATATVEQTKANQDLQDHIQAIGVGIAAGAIVASSFGLVTQPWYFPNREKIELPFLSPHPLIMALIFSGLCSVGSWLIARKVIEQKRGK
>NZ_CP051167.1|WP_168568715.1|2035703_2036729_+|hydrogenase-expression/formation-protein-HypE
MDFSCPIPIAQYPKILLAHGGGGKLMHQLIEQMFAPTFDAPATQHDSIVLTPPPGAIALTTDSYVINPLFFPGGDIGSLAVYGTVNDLAMSGARPLYLTVGFILEEGLPMETLWRVVQSMRQAADRCGVKIVTGDTKVVDRGKGDGIFINTAGVGVVEHSQAIAPPSVRPGDVLIVNGDLGRHGIAIMAVREGLEFETEIESDSAPAIREVSALLDAGIEIHCLRDLTRGGLASALNEIASAAAVDIAIDERSIPIREDVQAACEILGFDPLYVANEGRFVAFVPEEFAQKTLDILQRNDPRSRAIGRVTATGKGLVTMQSKIGASRIVDVLSGEQLPRIC
>NZ_CP051167.1|WP_168568716.1|2036889_2038335_-|DEAD/DEAH-box-helicase
MTLSFQSLGLSDARVEHLAKNGFTEPTAIQEQAIPHLLSGQDVVGQAQTGTGKTAAFSLPILEQLDPSDKTVQALVLTPTRELAIQVSNAISELNDDRRVRILSVYGGASIERQIQRLDRGVQIVVGTPGRVLDLLGRNSLKLDTLKWMVLDEADEMLSMGFIQDVEKILKAAPQEHQTAFFSATMDASIKALIRKFMNDPITVAIEMKTTPKRIEQAVYMVPRGWSKSRALQPILELEDPESAIVFVRTRRAAAELTSQLQAAGHSADEYHGDLNQSQRERLLHRFRQQQVRWIVATDIAARGLDVDHLTHVINYDLPDSVESYVHRIGRTGRAGREGTAISLILPYDRRKLRQIEDRVGQRFDIRSIPTRSQIEARHLEKLQTQVHEVLAGERLASFLPIVAQLSEEYDPHAIAAAALQLAYDRIRPNWAESEAPEEPIPVYSSKPRRNGDRRTPRPRKSFEPPKKKRSSRREPIGDRK
>NZ_CP051167.1|WP_168568717.1|2038644_2040000_-|30S-ribosomal-protein-S12-methylthiotransferase-RimO
MGNKPTIAISHLGCEKNRIDTEHMLGLLVEAGYNVDTNEELADYVIVNTCSFIQAAREESVRTLVGLAEEQKKIVITGCMAQHFQEQLLEELPEAVALVGTGDYHKIVQVIERAETGERVKEVSAEPTYIADETTPRYRTTSEGVAYLRIAEGCNYRCAFCIIPHLRGNQRSRSIESIVAEARQLAAQGVKEIILISQITTNYGTDIYGEPKLAELLRALGKVDIPWIRMHYAYPTGLTPPVIKAIRETPNVLPYLDLPLQHSHPQVLRSMNRPWQAGVNDSIIERLKEALPEAVLRTTFIVGFPGETDEQFDHLLQFVQRHEFDHVGVFTFSPEEGTPAYDLPNQISPEVMEARRDALMQMQQPIALKRNRTQVGKVVDVLIEQENPATGQYIGRSARFSPDVDGLVYVRGKARLGSMIPVLIENADIYDLSGRVARAADALQRESVVVS
>NZ_CP051167.1|WP_168568718.1|2040139_2040304_-|hypothetical-protein
MASVRTQVGMPRKEIPVLISGYPGKSKAQTPSILTDFVGAIAAELAIGGNRPKF
>NZ_CP051167.1|WP_168568719.1|2040350_2040491_+|hypothetical-protein
MSDLNRGIMKFKGADSPVAVALSSIAILGGIAFLIWWALQSAYTLN
>NZ_CP051167.1|WP_168568720.1|2040812_2041955_+|HlyC/CorC-family-transporter
MIASSFDSPLIAAAQPAPLLGNVWLDVGVLIFLLVLSGFFSGSETAITSLDNLKLRSLIQEQGDPTRIFTLVLHKRTRFITTLLVGNNLVNNFSAILTSNLFALWLGNTGLGIATALITFLLLIFGEITPKSLAINNSMSYFKISVRPIYWLSQFLAFFGIVQLLENIAQTVIRWVQSDRVQQGESVKDLQLMIEILGGKGHLDLYKHQLLNKALMLDSLSAREVVKPRIEMRTISHEASLQDLVDLCLETGYSRIPVQEESKDRIVGVVHLKRAIGQLTALQKEGTANGPVTMAMDPPVYVPETKRIADLLKEMLQQRLHLAIVVDEYGGTVGLLTLEDILEELVGEIYDESDFPMRMQRNRQGDRSHSNRPPKRGSRG

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Crispr_ID: NZ_CP051167_9

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_9

2026931-2027094

Orphan

N:A

Consensus_repeat	Method
GGGGAAGGGGTTTATACTTTTGCCA	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP051167_9

>merge|NZ_CP051167|9|2026931-2027094|CRISPRCasFinder
GGTGAAGGAGTCTATACCTTTGCCAGTGGTACCCGTTGTGAAGGCGAACTAATTGACGGAAAAATTACCGGGCAAGCGGTTTGTAACTATGCCAATGGCAACCGTTACGAAGGTAATTTAACCGATAGCGTTCCCGACGGCGAAGGCGTTTATATTTTTGCCGA

>NZ_CP051167|9|8|2026931-2027094|CRISPRCasFinder
GGTGAAGGAGTCTATACCTTTGCCA	GTGGTACCCGTTGTGAAGGCGAACTAATTGACGGAAAAATTACC
GGGCAAGCGGTTTGTAACTATGCCA	ATGGCAACCGTTACGAAGGTAATTTAACCGATAGCGTTCCCGAC
GGCGAAGGCGTTTATATTTTTGCCGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168568709.1\|2023423_2023828_-\|biopolymer-transporter-ExbD	unknown	unknown	gnl\|CDD\|223917
NZ_CP051167.1\|WP_168571803.1\|2014829_2016143_+\|lysine-N(6)-hydroxylase/L-ornithine-N(5)-oxygenase-family-protein	unknown	unknown	gnl\|CDD\|226017
NZ_CP051167.1\|WP_168568711.1\|2024888_2026394_+\|TonB-family-protein	unknown	unknown	gnl\|CDD\|367555
NZ_CP051167.1\|WP_168568706.1\|2017380_2019216_+\|IucA/IucC-family-siderophore-biosynthesis-protein	unknown	unknown	gnl\|CDD\|226715
NZ_CP051167.1\|WP_168568719.1\|2040350_2040491_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568718.1\|2040139_2040304_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568710.1\|2023811_2024459_-\|MotA/TolQ/ExbB-proton-channel-family-protein	unknown	unknown	gnl\|CDD\|223881
NZ_CP051167.1\|WP_168571805.1\|2030363_2034191_+\|CHAT-domain-containing-protein	unknown	unknown	gnl\|CDD\|378942
NZ_CP051167.1\|WP_168568704.1\|2014215_2014821_+\|acetyltransferase	unknown	unknown	gnl\|CDD\|379237
NZ_CP051167.1\|WP_043468426.1\|2029270_2029465_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568715.1\|2035703_2036729_+\|hydrogenase-expression/formation-protein-HypE	unknown	unknown	gnl\|CDD\|100033
NZ_CP051167.1\|WP_168568705.1\|2016142_2017339_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|340883
NZ_CP051167.1\|WP_168568716.1\|2036889_2038335_-\|DEAD/DEAH-box-helicase	unknown	unknown	gnl\|CDD\|223587
NZ_CP051167.1\|WP_168568714.1\|2034187_2035570_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571804.1\|2021267_2023223_+\|iron-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|236720
NZ_CP051167.1\|WP_168568720.1\|2040812_2041955_+\|HlyC/CorC-family-transporter	unknown	unknown	gnl\|CDD\|224173
NZ_CP051167.1\|WP_168568707.1\|2019339_2020134_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224045
NZ_CP051167.1\|WP_168568713.1\|2028801_2029251_+\|type-II-toxin-antitoxin-system-VapC-family-toxin	unknown	unknown	gnl\|CDD\|350222
NZ_CP051167.1\|WP_168568708.1\|2020171_2021104_+\|iron-siderophore-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|238566
NZ_CP051167.1\|WP_168568717.1\|2038644_2040000_-\|30S-ribosomal-protein-S12-methylthiotransferase-RimO	unknown	unknown	gnl\|CDD\|273453

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168568709.1\|2023423_2023828_-\|biopolymer-transporter-ExbD	gnl\|CDD\|223917	COG0848, ExbD, Biopolymer transport protein [Intracellular trafficking and secretion].	1.47856e-29
NZ_CP051167.1\|WP_168571803.1\|2014829_2016143_+\|lysine-N(6)-hydroxylase/L-ornithine-N(5)-oxygenase-family-protein	gnl\|CDD\|226017	COG3486, IucD, Lysine/ornithine N-monooxygenase [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP051167.1\|WP_168568711.1\|2024888_2026394_+\|TonB-family-protein	gnl\|CDD\|367555	pfam03544, TonB_C, Gram-negative bacterial TonB protein C-terminal. The TonB_C domain is the well-characterized C-terminal region of the TonB receptor molecule. This protein is bound to an inner membrane-bound protein ExbB via a globular domain and has a flexible middle region that is likely to help in positioning the C-terminal domain into the iron-transporter barrel in the outer membrane. TonB_C interacts with the N-terminal TonB box of the outer membrane transporter that binds the Fe3+-siderophore complex. The barrel of the transporter, consisting of 22 beta-sheets and an inside plug, binds the iron complex in the barrel entrance.	1.55651e-16
NZ_CP051167.1\|WP_168568706.1\|2017380_2019216_+\|IucA/IucC-family-siderophore-biosynthesis-protein	gnl\|CDD\|226715	COG4264, RhbC, Siderophore synthetase component [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP051167.1\|WP_168568710.1\|2023811_2024459_-\|MotA/TolQ/ExbB-proton-channel-family-protein	gnl\|CDD\|223881	COG0811, TolQ, Biopolymer transport proteins [Intracellular trafficking and secretion].	7.30879e-49
NZ_CP051167.1\|WP_168571805.1\|2030363_2034191_+\|CHAT-domain-containing-protein	gnl\|CDD\|378942	pfam12770, CHAT, CHAT domain. These proteins appear to be related to peptidases in peptidase clan CD that includes the caspases. This domain has been termed the CHAT domain for Caspase HetF Associated with Tprs. This family has been identified as a sister group to the separins.	4.48814e-45
NZ_CP051167.1\|WP_168568704.1\|2014215_2014821_+\|acetyltransferase	gnl\|CDD\|379237	pfam13523, Acetyltransf_8, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.55332e-67
NZ_CP051167.1\|WP_168568720.1\|2040812_2041955_+\|HlyC/CorC-family-transporter	gnl\|CDD\|224173	COG1253, TlyC, Hemolysins and related proteins containing CBS domains [General function prediction only].	6.91918e-84
NZ_CP051167.1\|WP_168568715.1\|2035703_2036729_+\|hydrogenase-expression/formation-protein-HypE	gnl\|CDD\|100033	cd02197, HypE, HypE (Hydrogenase expression/formation protein). HypE is involved in Ni-Fe hydrogenase biosynthesis. HypE dehydrates its own carbamoyl moiety in an ATP-dependent process to yield the enzyme thiocyanate. The N-terminal domain of HypE is related to the ATP-binding domains of the AIR synthases, selenophosphate synthetase (SelD), and FGAM synthase and is thought to bind ATP.	5.30151e-169
NZ_CP051167.1\|WP_168568705.1\|2016142_2017339_+\|MFS-transporter	gnl\|CDD\|340883	cd17325, MFS_MdtG_SLC18_like, bacterial MdtG-like and eukaryotic solute carrier 18 (SLC18) family of the Major Facilitator Superfamily of transporters. This family is composed of eukaryotic solute carrier 18 (SLC18) family transporters and related bacterial multidrug resistance (MDR) transporters including several proteins from Escherichia coli such as multidrug resistance protein MdtG, from Bacillus subtilis such as multidrug resistance proteins 1 (Bmr1) and 2 (Bmr2), and from Staphylococcus aureus such as quinolone resistance protein NorA. The family also includes Escherichia coli arabinose efflux transporters YfcJ and YhhS. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. The SLC18 transporter family includes vesicular monoamine transporters (VAT1 and VAT2), vesicular acetylcholine transporter (VAChT), and SLC18B1, which is proposed to be a vesicular polyamine transporter (VPAT). The MdtG/SLC18 family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.75131e-15
NZ_CP051167.1\|WP_168568716.1\|2036889_2038335_-\|DEAD/DEAH-box-helicase	gnl\|CDD\|223587	COG0513, SrmB, Superfamily II DNA and RNA helicases [DNA replication, recombination, and repair / Transcription / Translation, ribosomal structure and biogenesis].	6.98807e-160
NZ_CP051167.1\|WP_168571804.1\|2021267_2023223_+\|iron-ABC-transporter-permease	gnl\|CDD\|236720	PRK10577, PRK10577, Fe(3+)-hydroxamate ABC transporter permease FhuB.	0
NZ_CP051167.1\|WP_168568707.1\|2019339_2020134_+\|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].	1.88463e-121
NZ_CP051167.1\|WP_168568713.1\|2028801_2029251_+\|type-II-toxin-antitoxin-system-VapC-family-toxin	gnl\|CDD\|350222	cd09874, PIN_MT3492-like, VapC-like PIN domain of the hypothetical protein MT3492 of Mycobacterium tuberculosis CDC1551 and other uncharacterized, annotated PilT protein domain proteins. Virulence associated protein C (VapC)-like PIN (PilT N terminus) domain of Mycobacterium tuberculosis CDC1551, hypothetical protein MT3492, and similar bacterial and archaeal proteins are included in this subfamily. They are PIN domain homologs of the Mycobacterium tuberculosis VapC and Neisseria gonorrhoeae FitB toxins of the prokaryotic toxin/antitoxin operons, VapBC and FitAB, respectively, which are believed to be involved in growth inhibition by regulating translation. These toxins are nearly always co-expressed with an antitoxin, a cognate protein inhibitor, forming an inert protein complex. Disassociation of the protein complex activates the ribonuclease activity of the toxin by an, as yet undefined mechanism. The PIN domain belongs to a large nuclease superfamily. The structural properties of the PIN (PilT N terminus) domain indicate its active center, consisting of three highly conserved catalytic residues which coordinate metal ions, in some members, additional metal coordinating residues can be found. Some members of the superfamily lack several of these key catalytic residues. The PIN active site is geometrically similar in the active center of structure-specific 5' nucleases, PIN-domain ribonucleases of eukaryotic rRNA editing proteins, and bacterial toxins of toxin-antitoxin (TA) operons.	0.00024842
NZ_CP051167.1\|WP_168568708.1\|2020171_2021104_+\|iron-siderophore-ABC-transporter-substrate-binding-protein	gnl\|CDD\|238566	cd01146, FhuD, Fe3+-siderophore binding domain FhuD. These proteins have been shown to function as initial receptors in ABC transport of Fe3+-siderophores in many eubacterial species. They belong to the TroA-like superfamily of helical backbone metal receptor proteins that share a distinct fold and ligand binding mechanism. A typical TroA-like protein is comprised of two globular subdomains connected by a long alpha helix and binds its specific ligands in the cleft between these domains.	3.78231e-77
NZ_CP051167.1\|WP_168568717.1\|2038644_2040000_-\|30S-ribosomal-protein-S12-methylthiotransferase-RimO	gnl\|CDD\|273453	TIGR01125, Ribosomal_protein_S12_methylthiotransferase_RimO, ribosomal protein S12 methylthiotransferase RimO. Members of this protein are the methylthiotransferase RimO, which modifies a conserved Asp residue in ribosomal protein S12. This clade of radical SAM family proteins is closely related to the tRNA modification bifunctional enzyme MiaB (see TIGR01574), and it catalyzes the same two types of reactions: a radical-mechanism sulfur insertion, and a methylation of the inserted sulfur. This clade spans alpha and gamma proteobacteria, cyano bacteria, Deinococcus, Porphyromonas, Aquifex, Helicobacter, Campylobacter, Thermotoga, Chlamydia, Streptococcus coelicolor and Clostridium, but does not include most other gram positive bacteria, archaea or eukaryotes. [Protein synthesis, Ribosomal proteins: synthesis and modification].	0

>NZ_CP051167.1|WP_168568711.1|2024888_2026394_+|TonB-family-protein
MSVYGVYSSQRERQEKQIERFIGWSLLGSIALHVAILPLGLQLLAQEPRTVTEEAIEFIVVEKPEVEEPEVEEPTVEEPEIEEPPIEEPPIEESYRSPTETISESSPRESFSEPESIPESPTEPTRPLFDTQNNVDNFDRADSPEIARSISEPQEPQEPQEPREIAPPVTQSPAITDSSEKPAISEPEMPESEISETPSSSFDEPTSPPISEPELSSPPNDPIASPAIEDPTEAIEEFTTTEPPEIARNYENPDIESDFDPGSTEAEFSEPEIASESSAPAVQPPMYNDPSPSDTWDASEPNDPIASSYNDYSTSSRDETGSMAPLDESNPYAESEIGSNAPISSSYSAPIADSTGDSSNFLNETPSYDDSSSSYDSYDAPSNDWDPGASSGFDEPAIANSGPMGDLPNSSSSGSGSGSVGCINCGKPSYPDIAREQGWEGEVLLSVDVDPNGNVSNVQLISSSGYPVLDNTAIDRAWSWQFDSSENGQQGRMVSVPFELR
>NZ_CP051167.1|WP_168568710.1|2023811_2024459_-|MotA/TolQ/ExbB-proton-channel-family-protein
MLDIIAAGGLVAWPLLIASVVAVALVAERSYFWFRIRKRGRKVAKDALQTYLQDPQAAFSKLGMNTDLPIARIFLEALELNDPNPEEFRLALESAVQAEIPVLKRFNTVFETIVNVAPLLGLLGTILGLMNAFSSLQLGDVGGTDTVGVTGGISEALVSTVMGLIVAIFTLLFTNMFRSFYLRELALIQEAGGQLELFYRHRYEREQEKTYASTR
>NZ_CP051167.1|WP_168568709.1|2023423_2023828_-|biopolymer-transporter-ExbD
MRVPDEPENSPQINIVPMIDIIFSILAYFIISSLFLSKSEGLPVNLPKASTAQVQAETRKMTITLDAEGVISLDKEEIELDSLEENLRDRIEKEGESLVILNADEALDHGRVVAVMDKVRRIEGAKLAIAAKKQ
>NZ_CP051167.1|WP_168571804.1|2021267_2023223_+|iron-ABC-transporter-permease
MLLAIAHLAQGEIEIDLLTVLGAVFAPDGSPNAQIVRSLRLPRSAIAVMTGAAWGMAGVLFQTVTRNPLSSAATLGINAGAYFSVTAALIFVPQWFDRSPVGVALAGGILAAALVYAIAAGVHLSPLRLTLSGVAVSLALASLTAILQVFYENQLSGIFLWGAGSLRQTDWSNAAYAAPRIAIPATFALLLSKNWDILLLGDDVARSLGQNLQKTRMICTAIAVFLAALSVSVVGPIGFIGIVAPHLVRLMGCRSHWTLLPAAAIWGAIVLVGADICALQFSAGFGEIPVGTTIPLVGAPFLIWLVGKNERLDRGSSPARSSSHQGRSYPYPALTLAAIGLIFVAAIASLSLGTLSSSPGKFLALIAGNASELYTWVVFELRLPRLVVSLLAGSSLAVSGLLLQSVVRNPIAGPEIVGITSGAGLGVCFILVLFPGASVEAVAIAAFVGAFAVFALIGAIAWRSNLSPTRLALVGIAVSAFCTAGINLLVVVAQLRVARALVWLAGSTYARNWEDIARLSPWPLVLLPLAWVFAPWLDLMALGEDLPRLLGVQLQKARALAISIAVALAAAAVSTVGTISFVGLVAPHIARLLVGSRHRQLVPLAALFGALLVAVADTLGRIVVAPAEIPSGLVTAAIGTPYFLWLLWRSR
>NZ_CP051167.1|WP_168568708.1|2020171_2021104_+|iron-siderophore-ABC-transporter-substrate-binding-protein
MLKKPSKFLKLLVCFLLGVFIFSCTSDRPQLNLKVNGEYPKRIVALEWVYVEDLLTLGIQPVGVADITGYQQFVQIEPQLAEDVVDVGTRQEPNLEAIAELDPDLIIGVQFRHEYIKETLSKIAPTLLFNPYPPPPPQGIRQLDEMQATFLKIAETVGQAERGKAVLKQMHSNFDRISQQLKGIGLDDAKFVLGQLPPIGPELRLFNESSMAVQILQEIGLNNLWKGNSNSFGFNSVWVESLPQIETAHFFYISNKSNPYLELLTNNFVWKNLKFVKEDRVYSLDGQTWLFGGPLSAELLGKNVIKNLVK
>NZ_CP051167.1|WP_168568707.1|2019339_2020134_+|ABC-transporter-ATP-binding-protein
MIAATDWAIRAINLKISYDDLAIVSDLSIDIEMGKITALIGPNGSGKSTVLRTIARLLKPERGLIYLNGKNIAKMPTQAIARELAMLPQSPDIPAGITVWELIGYGRYPHRSLLGTLSRQDKIAMEWALEMTRLQSLRDRAVDTLSGGERQRAWIALALAQKTGILLLDEPTTFLDIRHQLDILSLVKSLNREQQITVVWVLHELNQAAAYSDRMIMFRSGEIMSMGTPAQVMTPEKILEVFGVKMTVIPHPVNGLPTCFPINY
>NZ_CP051167.1|WP_168568706.1|2017380_2019216_+|IucA/IucC-family-siderophore-biosynthesis-protein
MKNLDTLNATLQSQRWQNVSQKLLAKMLSEFMYEEIVKPECLQQTGDRQALYKLSLPEGIAYQFEAKQRLFDSYRVKPDSIQRWDGQIWQQGSSPFQFVLDCHTAVGMTVETAGHLIKELSQTLLADAHIDRQKSEQQSEQQTDLLALDYAHLEGKMEGHPWITFNKGRIGFGYADYLAHAPENQQPVHLPWLAVSKKTAQFNAIADLDYEQAIAEELSASDLAQFKAILTAQNRNPDNYLLMPVHDWQWDNKIIPIFAEEIAKGKIVYLGKSSDLYLPQQSIRTFVNISNPHKRHVKLPLSILNTLVYRGLPGERTAIAPKVTEWITSIWKNDSFLSQKCRLILPGEVASINYEHPYFTALHGAPYQYKEMLGCLWRESVLSYCETDEKLITLAALVHIDGNGKPFVSQLIEKSGLSPQVWLDRLFNTVLPPLLHYLYRYGVVFSPHGENTILVLKDYIPHRLAMKDFVDDVNVSRHPLPELESIPADLKGILLSEPPEGLCQFIFAGLFICHHRYLSDILEEFHQYDERDFWQQVRQVILNYQRQFPELQDRFELFNLLAPKFTKLCLNRNRLITYGYADDGDRPHAAAFGKVNNALHEAISDRLNLSV
>NZ_CP051167.1|WP_168568705.1|2016142_2017339_+|MFS-transporter
MKVNPKWIPIALFSCVFISIFTEVLLSPFYPQFFSKVFGIEDLSYTGYYIFICRLTVVLCAPLWGVFSRWIEVKYLLYCAQIGTAFFTALMATSTSANCFLAYTIGLLLFKSCYLMVYPLIIQLTDSQQHSTVTGTYQAVFHGGIIAATIAGAWMVNLEAPLSLFYAIAIADLFQFLLCFIFLRDTQTRREITPPSEQHSSFGDRWGFIVAIGLIILTFQLANNLIRPFFTAYVTQSETLGITLNESSYLFMIPSAMAIAALPYIRKSFHRDRLHSIYLVGLVLLSVTLFLQGWTISLGILIIARLIYGFCLATSQSALELRLFDRSRGDRLHFNYSLAMSFANLGHLSAPLLASWLVERYTLAMPLFVAAFICAVNFLFAQKTIFRAPIFQPSEVEL
>NZ_CP051167.1|WP_168571803.1|2014829_2016143_+|lysine-N(6)-hydroxylase/L-ornithine-N(5)-oxygenase-family-protein
MNGKIYDLIGVGLGPFNLGLAALLDQTNLDCLFLEQKPEFQWHPGLLIENSTIQVPFLADLVTMADPCSPYSFLNYLHAQSRLYHFYFFEKFHIPRREYNHYCRWVSQQLNSCQFGQRVESLTLENIDFETYYKIESRELKTGKMNTYFAHHLVLGVGSIPQVPPCFQNIYSDHIFHSAEFLNRRDRALQSDSITVIGSGQSAAEVFYELLQQQSNYSYRLEWHTRSAGFLPMEYSKLGLEHFSPDYIDYFYHLPPQKRDRLLSEQRLLYKGISFETIADIYDLLYERSIGGQPLNVRLLPLVEVKEVERVTTEKGDRFVLGYRHSQQETRFTHETDCVILATGYRHAIPRCIDGIRDLIQWDSRGRYEVKFDYRLALNREISNHIFVQNGELHTHGIGAPDLGLGAHRNSVIINTLLGETVYPVERRNVFQQFGVA
>NZ_CP051167.1|WP_168568704.1|2014215_2014821_+|acetyltransferase
MKFPQTEEKLQFSYKKFDRSLEKTIAFRPVELEKDLDRIHRWMNEPHVIPFWQLNFDRDRMRSHLEKALSDRHQTLYIGYLDGVPMSYWEAYWAKDDAIAQCYEPDAGDRGIHLLIGEPKFLGKGYALPLLRAMTNLQFEFSATPKLQTQKVVTEPDIRNAKMIHIFKRCGFVFQREIELPDKRAALMFCDRQSFRKKSEQ
>NZ_CP051167.1|WP_168568713.1|2028801_2029251_+|type-II-toxin-antitoxin-system-VapC-family-toxin
MVAVYLDVCCLNRPFDDWAQERVRLEGDSVLTILERVRTGEWQLISSEAILVELEKMRNLEKKTSILSLLALATQMQEINPTVEERSQQLEGFGFGLFDSFHLACAEAAGADIFLSTDDRLLKTARRYASQLKVAISNPVVWLIQVLQE
>NZ_CP051167.1|WP_043468426.1|2029270_2029465_+|hypothetical-protein
MNAVELREKGYQILVNHLGQSDAIRFLQQMGWGQGDYTQERRDVLESVTREEFLEDLRKIRGLQ
>NZ_CP051167.1|WP_168571805.1|2030363_2034191_+|CHAT-domain-containing-protein
MRQNMESIVPALGDTIAQWIQGVLTQQPDQAEGVAGLVENTCISIQEFPYGRYAEVQEIAIRGYDLVLALRANQPEKRAQTLTNLGVAYLTQAQFGLDPAANLDQAIAAYTEAAAIRRRPGLEKDLASTLNNLGNAYQTQAQFGLDPAANLDQAIAAYTEAAAIRRRPGLEKDLASTLNNLGNAYQTQAQFGLDPAANLDQAIAAYTEAAAIMRRPGLEKDLASTLTNLGVAYLTQAEFGLDPAANLDQAIAAYTEAAAIRRRPGLEKDLASTLNNLGNAYQTQAQFGLDPAANLDQAIAAYTEAAAIRRRPGLEKDLASTLTNLGVAYLTQAEFGLDPAANLDQAIAAYTEAAAIRRRPGLEKDLASTLTNLGVAYLTQAEFGLDPAANLDQAIAAYTEAAAIRRRPGLEKDLASTLNNLGNAYQTQAQFGLDPAANLDQAIAAYTEAAAIRRRPGLEKDLASTLTNLGVAYLTQAEFGLDPAANLDQAIAAYTEAAAIMRRPGLEKDLASTLTNLGVAYRTQAEFGLDPAANLDQAIAAYTEAAAIMRRPGLEKDLASTLTNLGVAYLTQAEFGLDPAANLDQAIAAYTEAAAIMRRPGLEKDLASTLNNWGFTYQQQSQYYSSDPERKQTALENAYRTFAEALEQVEYLRGEITTEDYKRNFNEQWNKIYRGMVEVCLELGNYTAAIEYADRSKARNLVELIATRDAYPQGISPEDRQRLQQLRQAIFQEDRRLQQDPNRDSSHLNQLRDEFQKKFPYQPLHFPQIQQLLDEETAILEWYILGDKFLTFTLTAQTLHLWTSSPEDLEKLGEWGNAYLNDYRRNKTQWQDNLQQRLDSLTQILHLDEILQNLRENFPNCQKLILIPHRYLHLFPIHALPVLTGENQSQTLQELFPKGVNYAPSCQLLQQAQNRPRRHFTHFFAVQNPTEDLTFADVEVETIRSLFPQRRSLQRNNATKATFLAKDLSQTHHLFFSCNAEFNPNSPLDSGLQLADGILTLEEIIASLNLSECSLVTLSACESGQVALDQTDEYISLSSGFILAGSPSILVSLWFVDEVSTALLLIKTYETLQQHPGQLAIALKTAQIWLRDTTVAGFQDWVQKCPLLGDWRDALAEFFQNLGQNEKGINDRPYKSPYHWAAFCVVGQGEQNMASDRDKIQAFIKLIQENPDNLFADHWSSLTELPNQFTDDDEKNVELIEQWVKEPTRTDIYQVYQDRYRSANPLLGATGHKGGFGSQQTPKEAGKSSGELIDQAIKHNTTRPDSPRQSPQNES
>NZ_CP051167.1|WP_168568714.1|2034187_2035570_+|hypothetical-protein
MKNFSLSLYAFHLRQALDDPPDSVNPEADRLWESLTQLSKVLDFPELKNLKSQLICYSPDSDNRPQYHPQAENTLRYEWLSHHAGEVKFTAIPTPAGFKLGGKLQPFRLHDTYCVDLTLSPDPQDLELGVENLGCFHPKDLVSQIEANLGKFVWLTGYSTESELPKQAEAWVNAFCAKTGLIPEFIEGGKLFHADCFLYEAQNITILISIANPNNSTEVEQSANDNYDRFRNLLWSRQKILFVQEKAKQCYENTRKIYSQLENQINSFYELFESPTEARLKKLDSLLTSLPKDLLEYNCYLRDLKAHYTTLDTNAQNFKTCLDRVIQPGDNLQTWADFAEKICPRFLTQIKTYINYLEPGKELFTELVNTIRATATVEQTKANQDLQDHIQAIGVGIAAGAIVASSFGLVTQPWYFPNREKIELPFLSPHPLIMALIFSGLCSVGSWLIARKVIEQKRGK
>NZ_CP051167.1|WP_168568715.1|2035703_2036729_+|hydrogenase-expression/formation-protein-HypE
MDFSCPIPIAQYPKILLAHGGGGKLMHQLIEQMFAPTFDAPATQHDSIVLTPPPGAIALTTDSYVINPLFFPGGDIGSLAVYGTVNDLAMSGARPLYLTVGFILEEGLPMETLWRVVQSMRQAADRCGVKIVTGDTKVVDRGKGDGIFINTAGVGVVEHSQAIAPPSVRPGDVLIVNGDLGRHGIAIMAVREGLEFETEIESDSAPAIREVSALLDAGIEIHCLRDLTRGGLASALNEIASAAAVDIAIDERSIPIREDVQAACEILGFDPLYVANEGRFVAFVPEEFAQKTLDILQRNDPRSRAIGRVTATGKGLVTMQSKIGASRIVDVLSGEQLPRIC
>NZ_CP051167.1|WP_168568716.1|2036889_2038335_-|DEAD/DEAH-box-helicase
MTLSFQSLGLSDARVEHLAKNGFTEPTAIQEQAIPHLLSGQDVVGQAQTGTGKTAAFSLPILEQLDPSDKTVQALVLTPTRELAIQVSNAISELNDDRRVRILSVYGGASIERQIQRLDRGVQIVVGTPGRVLDLLGRNSLKLDTLKWMVLDEADEMLSMGFIQDVEKILKAAPQEHQTAFFSATMDASIKALIRKFMNDPITVAIEMKTTPKRIEQAVYMVPRGWSKSRALQPILELEDPESAIVFVRTRRAAAELTSQLQAAGHSADEYHGDLNQSQRERLLHRFRQQQVRWIVATDIAARGLDVDHLTHVINYDLPDSVESYVHRIGRTGRAGREGTAISLILPYDRRKLRQIEDRVGQRFDIRSIPTRSQIEARHLEKLQTQVHEVLAGERLASFLPIVAQLSEEYDPHAIAAAALQLAYDRIRPNWAESEAPEEPIPVYSSKPRRNGDRRTPRPRKSFEPPKKKRSSRREPIGDRK
>NZ_CP051167.1|WP_168568717.1|2038644_2040000_-|30S-ribosomal-protein-S12-methylthiotransferase-RimO
MGNKPTIAISHLGCEKNRIDTEHMLGLLVEAGYNVDTNEELADYVIVNTCSFIQAAREESVRTLVGLAEEQKKIVITGCMAQHFQEQLLEELPEAVALVGTGDYHKIVQVIERAETGERVKEVSAEPTYIADETTPRYRTTSEGVAYLRIAEGCNYRCAFCIIPHLRGNQRSRSIESIVAEARQLAAQGVKEIILISQITTNYGTDIYGEPKLAELLRALGKVDIPWIRMHYAYPTGLTPPVIKAIRETPNVLPYLDLPLQHSHPQVLRSMNRPWQAGVNDSIIERLKEALPEAVLRTTFIVGFPGETDEQFDHLLQFVQRHEFDHVGVFTFSPEEGTPAYDLPNQISPEVMEARRDALMQMQQPIALKRNRTQVGKVVDVLIEQENPATGQYIGRSARFSPDVDGLVYVRGKARLGSMIPVLIENADIYDLSGRVARAADALQRESVVVS
>NZ_CP051167.1|WP_168568718.1|2040139_2040304_-|hypothetical-protein
MASVRTQVGMPRKEIPVLISGYPGKSKAQTPSILTDFVGAIAAELAIGGNRPKF
>NZ_CP051167.1|WP_168568719.1|2040350_2040491_+|hypothetical-protein
MSDLNRGIMKFKGADSPVAVALSSIAILGGIAFLIWWALQSAYTLN
>NZ_CP051167.1|WP_168568720.1|2040812_2041955_+|HlyC/CorC-family-transporter
MIASSFDSPLIAAAQPAPLLGNVWLDVGVLIFLLVLSGFFSGSETAITSLDNLKLRSLIQEQGDPTRIFTLVLHKRTRFITTLLVGNNLVNNFSAILTSNLFALWLGNTGLGIATALITFLLLIFGEITPKSLAINNSMSYFKISVRPIYWLSQFLAFFGIVQLLENIAQTVIRWVQSDRVQQGESVKDLQLMIEILGGKGHLDLYKHQLLNKALMLDSLSAREVVKPRIEMRTISHEASLQDLVDLCLETGYSRIPVQEESKDRIVGVVHLKRAIGQLTALQKEGTANGPVTMAMDPPVYVPETKRIADLLKEMLQQRLHLAIVVDEYGGTVGLLTLEDILEELVGEIYDESDFPMRMQRNRQGDRSHSNRPPKRGSRG

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Crispr_ID: NZ_CP051167_11

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_11

2127509-2129520

Unclear

N:A

Consensus_repeat	Method
CTTTCAATTAACTGAATCCCGGCAACGGG---------ATTGAAAC	PILER-CR
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CRISPRCasFinder
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CRT

27 spacers

Cas14u_CAS-V

The CRISPR arrays of NZ_CP051167_11

>merge|NZ_CP051167|11|2127509-2129520|PILER-CR,CRISPRCasFinder,CRT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACACTATGCACATCGGCGACAAGGTGCGCAATCGTCTCCCGGCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACTATTCACCCCATCGCTTTCACTACCGGACTGACCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACATTACAGCTCTAGTATAGAATGGTAAAGGATACTTTCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACTTCTGATGGAAAGCTTTGGGATTTCATGATTTCCTCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACCTACCTCAACAATAACTTCGAGAAGAAACTCAACTCCGACTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACTTTATCGAAGGGGGGGCGATCGAGATCGAGGGAGACTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACCCAAGCGGTATCCTACCTGGGCGCATACATATTGCCGGCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACCTAAGTGAGAAAGAGGCGAACGAAAGCATTTTAGACTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACTACTCGTATCTAGACCAATTTTTTCGCTTTCTGCGTTCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACTAGCACTTTTCTGCTTTGAAGTGAGATTATCTCCGCTCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACCCCGATCGATTTCCGACATCTCCTTGATCGTTCGCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACCAATTTGGCCTGAGCATGCGCAGCAGCTCGAAGCTGCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACCAGACTAACTGTCAAAATTGCCGCCGCTCGATTTCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACGAACCTCAAATGAACGATATCGGCATCCATGACTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACCGATCTGTCGCTGAATGATTCATGGTTTGTTTTCTAACTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACCACGCGCATCATGGCATCCTCGCTGGATTCGGGGATCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACTTTATATATATCTGAGGTACTATCTAATATCTGATTTCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACATGAGTAACCCTTTAGCTGCCCGACGAATGAAGCCTCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACTTATCGGTAAATAGTAGAGTATGGGCTAATAATACTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACTGAGCTACTGTAGAGGTTGTTGAAGGTGATTGAGTCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACTAAATCGGCATGCACCAATCTTGATTTTTCAAGATTAGCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACCTTCTCTTTGCAGGATATTATTTAGAGCTTTTCGGGCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACTAGGGTTTCTTCCCAGGTGTTCGGAGAGGTGTTCGGAGACTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACGCAACAGACGATGAAATTCGAGCGCATTTAGACAACAACTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACCGGGCGAAGGCAGCGACTTTCGCAACGGCTCAACTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACGAGTCGCTGCTTGCGGAGTACATACGCTGATAAAGTTGCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAACGAATTCCTCTGGCAATGAGCGGCCACAGTCGCTCTTGTCTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC

>NZ_CP051167|11|8|2127509-2129520|PILER-CR
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	ACTATGCACATCGGCGACAAGGTGCGCAATCGTCTCCCGG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TATTCACCCCATCGCTTTCACTACCGGACTGAC
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	ATTACAGCTCTAGTATAGAATGGTAAAGGATACTTT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TTCTGATGGAAAGCTTTGGGATTTCATGATTTCCT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CTACCTCAACAATAACTTCGAGAAGAAACTCAACTCCGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TTTATCGAAGGGGGGGCGATCGAGATCGAGGGAGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CCAAGCGGTATCCTACCTGGGCGCATACATATTGCCGG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CTAAGTGAGAAAGAGGCGAACGAAAGCATTTTAGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TACTCGTATCTAGACCAATTTTTTCGCTTTCTGCGTT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TAGCACTTTTCTGCTTTGAAGTGAGATTATCTCCGCT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CCCGATCGATTTCCGACATCTCCTTGATCGTTCG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CAATTTGGCCTGAGCATGCGCAGCAGCTCGAAGCTG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CAGACTAACTGTCAAAATTGCCGCCGCTCGATTT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	GAACCTCAAATGAACGATATCGGCATCCATGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CGATCTGTCGCTGAATGATTCATGGTTTGTTTTCTAA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CACGCGCATCATGGCATCCTCGCTGGATTCGGGGAT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TTTATATATATCTGAGGTACTATCTAATATCTGATTT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	ATGAGTAACCCTTTAGCTGCCCGACGAATGAAGCCT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TTATCGGTAAATAGTAGAGTATGGGCTAATAATA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TGAGCTACTGTAGAGGTTGTTGAAGGTGATTGAGT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TAAATCGGCATGCACCAATCTTGATTTTTCAAGATTAG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CTTCTCTTTGCAGGATATTATTTAGAGCTTTTCGGG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TAGGGTTTCTTCCCAGGTGTTCGGAGAGGTGTTCGGAGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	GCAACAGACGATGAAATTCGAGCGCATTTAGACAACAA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CGGGCGAAGGCAGCGACTTTCGCAACGGCTCAA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	GAGTCGCTGCTTGCGGAGTACATACGCTGATAAAGTTG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	GAATTCCTCTGGCAATGAGCGGCCACAGTCGCTCTTGT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC

>NZ_CP051167|11|10|2127509-2129520|CRISPRCasFinder
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	ACTATGCACATCGGCGACAAGGTGCGCAATCGTCTCCCGG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TATTCACCCCATCGCTTTCACTACCGGACTGAC
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	ATTACAGCTCTAGTATAGAATGGTAAAGGATACTTT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TTCTGATGGAAAGCTTTGGGATTTCATGATTTCCT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CTACCTCAACAATAACTTCGAGAAGAAACTCAACTCCGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TTTATCGAAGGGGGGGCGATCGAGATCGAGGGAGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CCAAGCGGTATCCTACCTGGGCGCATACATATTGCCGG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CTAAGTGAGAAAGAGGCGAACGAAAGCATTTTAGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TACTCGTATCTAGACCAATTTTTTCGCTTTCTGCGTT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TAGCACTTTTCTGCTTTGAAGTGAGATTATCTCCGCT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CCCGATCGATTTCCGACATCTCCTTGATCGTTCG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CAATTTGGCCTGAGCATGCGCAGCAGCTCGAAGCTG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CAGACTAACTGTCAAAATTGCCGCCGCTCGATTT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	GAACCTCAAATGAACGATATCGGCATCCATGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CGATCTGTCGCTGAATGATTCATGGTTTGTTTTCTAA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CACGCGCATCATGGCATCCTCGCTGGATTCGGGGAT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TTTATATATATCTGAGGTACTATCTAATATCTGATTT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	ATGAGTAACCCTTTAGCTGCCCGACGAATGAAGCCT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TTATCGGTAAATAGTAGAGTATGGGCTAATAATA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TGAGCTACTGTAGAGGTTGTTGAAGGTGATTGAGT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TAAATCGGCATGCACCAATCTTGATTTTTCAAGATTAG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CTTCTCTTTGCAGGATATTATTTAGAGCTTTTCGGG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TAGGGTTTCTTCCCAGGTGTTCGGAGAGGTGTTCGGAGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	GCAACAGACGATGAAATTCGAGCGCATTTAGACAACAA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CGGGCGAAGGCAGCGACTTTCGCAACGGCTCAA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	GAGTCGCTGCTTGCGGAGTACATACGCTGATAAAGTTG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	GAATTCCTCTGGCAATGAGCGGCCACAGTCGCTCTTGT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC

>NZ_CP051167|11|4|2127509-2129520|CRT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	ACTATGCACATCGGCGACAAGGTGCGCAATCGTCTCCCGG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TATTCACCCCATCGCTTTCACTACCGGACTGAC
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	ATTACAGCTCTAGTATAGAATGGTAAAGGATACTTT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TTCTGATGGAAAGCTTTGGGATTTCATGATTTCCT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CTACCTCAACAATAACTTCGAGAAGAAACTCAACTCCGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TTTATCGAAGGGGGGGCGATCGAGATCGAGGGAGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CCAAGCGGTATCCTACCTGGGCGCATACATATTGCCGG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CTAAGTGAGAAAGAGGCGAACGAAAGCATTTTAGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TACTCGTATCTAGACCAATTTTTTCGCTTTCTGCGTT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TAGCACTTTTCTGCTTTGAAGTGAGATTATCTCCGCT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CCCGATCGATTTCCGACATCTCCTTGATCGTTCG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CAATTTGGCCTGAGCATGCGCAGCAGCTCGAAGCTG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CAGACTAACTGTCAAAATTGCCGCCGCTCGATTT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	GAACCTCAAATGAACGATATCGGCATCCATGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CGATCTGTCGCTGAATGATTCATGGTTTGTTTTCTAA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CACGCGCATCATGGCATCCTCGCTGGATTCGGGGAT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TTTATATATATCTGAGGTACTATCTAATATCTGATTT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	ATGAGTAACCCTTTAGCTGCCCGACGAATGAAGCCT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TTATCGGTAAATAGTAGAGTATGGGCTAATAATA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TGAGCTACTGTAGAGGTTGTTGAAGGTGATTGAGT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TAAATCGGCATGCACCAATCTTGATTTTTCAAGATTAG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CTTCTCTTTGCAGGATATTATTTAGAGCTTTTCGGG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	TAGGGTTTCTTCCCAGGTGTTCGGAGAGGTGTTCGGAGA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	GCAACAGACGATGAAATTCGAGCGCATTTAGACAACAA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	CGGGCGAAGGCAGCGACTTTCGCAACGGCTCAA
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	GAGTCGCTGCTTGCGGAGTACATACGCTGATAAAGTTG
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC	GAATTCCTCTGGCAATGAGCGGCCACAGTCGCTCTTGT
CTTTCAATTAACTGAATCCCGGCAACGGGATTGAAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168568791.1\|2139902_2141969_-\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|143635
NZ_CP051167.1\|WP_168568780.1\|2122789_2123918_+\|peptide-chain-release-factor-2	unknown	unknown	gnl\|CDD\|234799
NZ_CP051167.1\|WP_168571812.1\|2138572_2139649_-\|ferrochelatase	unknown	unknown	gnl\|CDD\|223353
NZ_CP051167.1\|WP_168568777.1\|2119984_2120434_-\|IS200/IS605-family-transposase	unknown	unknown	gnl\|CDD\|376616
NZ_CP051167.1\|WP_168568778.1\|2120450_2121785_+\|IS200/IS605-family-element-transposase-accessory-protein-TnpB	Cas14u_CAS-V	-	gnl\|CDD\|273793
NZ_CP051167.1\|WP_168568779.1\|2121856_2122582_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|376437
NZ_CP051167.1\|WP_168568782.1\|2124452_2124974_+\|rRNA-maturation-RNase-YbeY	unknown	unknown	gnl\|CDD\|234575
NZ_CP051167.1\|WP_168571809.1\|2125159_2125615_+\|diacylglycerol-kinase-family-protein	unknown	unknown	gnl\|CDD\|260134
NZ_CP051167.1\|WP_168571810.1\|2126411_2127215_+\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|316044
NZ_CP051167.1\|WP_168568786.1\|2132051_2132951_+\|tRNA-pseudouridine(55)-synthase-TruB	unknown	unknown	gnl\|CDD\|179469
NZ_CP051167.1\|WP_168568790.1\|2137457_2138468_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568788.1\|2134652_2134793_+\|ribbon-helix-helix-protein,-CopG-family	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571811.1\|2136923_2137112_+\|PspC-domain-containing-protein	unknown	unknown	gnl\|CDD\|377200
NZ_CP051167.1\|WP_168568787.1\|2133271_2134306_-\|mechanosensitive-ion-channel-family-protein	unknown	unknown	gnl\|CDD\|366370
NZ_CP051167.1\|WP_168568781.1\|2124230_2124440_+\|DUF3285-domain-containing-protein	unknown	unknown	gnl\|CDD\|314535
NZ_CP051167.1\|WP_168568776.1\|2118835_2119618_-\|RNA-polymerase-sigma-factor-SigF	unknown	unknown	gnl\|CDD\|180965
NZ_CP051167.1\|WP_168568785.1\|2130875_2131613_+\|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|379312
NZ_CP051167.1\|WP_168568783.1\|2125744_2126353_+\|aminodeoxychorismate/anthranilate-synthase-component-II	unknown	unknown	gnl\|CDD\|235552
NZ_CP051167.1\|WP_168568784.1\|2129682_2130465_-\|uroporphyrinogen-III-C-methyltransferase	unknown	unknown	gnl\|CDD\|235711
NZ_CP051167.1\|WP_168568789.1\|2134924_2136853_+\|S9-family-peptidase	unknown	unknown	gnl\|CDD\|224423

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168568791.1\|2139902_2141969_-\|diguanylate-cyclase	gnl\|CDD\|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	7.37591e-65
NZ_CP051167.1\|WP_168568780.1\|2122789_2123918_+\|peptide-chain-release-factor-2	gnl\|CDD\|234799	PRK00578, prfB, peptide chain release factor 2; Validated.	0
NZ_CP051167.1\|WP_168571812.1\|2138572_2139649_-\|ferrochelatase	gnl\|CDD\|223353	COG0276, HemH, Protoheme ferro-lyase (ferrochelatase) [Coenzyme metabolism].	1.3228e-74
NZ_CP051167.1\|WP_168568777.1\|2119984_2120434_-\|IS200/IS605-family-transposase	gnl\|CDD\|376616	pfam01797, Y1_Tnp, Transposase IS200 like. Transposases are needed for efficient transposition of the insertion sequence or transposon DNA. This family includes transposases for IS200 from E. coli.	1.1273e-43
NZ_CP051167.1\|WP_168568778.1\|2120450_2121785_+\|IS200/IS605-family-element-transposase-accessory-protein-TnpB	gnl\|CDD\|273793	TIGR01766, Putative_transposase_MJ0751, transposase, IS605 OrfB family, central region. This model represents a region of a sequence similarity between a family of putative transposases of Thermoanaerobacter tengcongensis, smaller related proteins from Bacillus anthracis, putative transposes described by pfam01385, and other proteins. [Mobile and extrachromosomal element functions, Transposon functions].	2.57651e-07
NZ_CP051167.1\|WP_168568779.1\|2121856_2122582_+\|hypothetical-protein	gnl\|CDD\|376437	pfam01027, Bax1-I, Inhibitor of apoptosis-promoting Bax1. Programmed cell-death involves a set of Bcl-2 family proteins, some of which inhibit apoptosis (Bcl-2 and Bcl-XL) and some of which promote it (Bax and Bak). Human Bax inhibitor, BI-1, is an evolutionarily conserved integral membrane protein containing multiple membrane-spanning segments predominantly localized to intracellular membranes. It has 6-7 membrane-spanning domains. The C termini of the mammalian BI-1 proteins are comprised of basic amino acids resembling some nuclear targeting sequences, but otherwise the predicted proteins lack motifs that suggest a function. As plant BI-1 appears to localize predominantly to the ER, we hypothesized that plant BI-1 could also regulate cell death triggered by ER stress. BI-1 appears to exert its effect through an interaction with calmodulin. The budding yeast member of this family has been found unexpectedly to encode a BH3 domain-containing protein (Ybh3p) that regulates the mitochondrial pathway of apoptosis in a phylogenetically conserved manner. Examination of the crystal structure of a bacterial member of this family shows that these proteins mediate a calcium leak across the membrane that is pH-dependent. Calcium homoeostasis balances passive calcium leak with active calcium uptake. The structure exists in a pore-closed and pore-open conformation, at pHs of 8 and 6 respectively, and the pore can be opened by intracrystalline transition; together these findings suggest that pH controls the conformational transition.	2.24878e-24
NZ_CP051167.1\|WP_168568782.1\|2124452_2124974_+\|rRNA-maturation-RNase-YbeY	gnl\|CDD\|234575	PRK00016, PRK00016, metal-binding heat shock protein; Provisional.	2.04962e-49
NZ_CP051167.1\|WP_168571809.1\|2125159_2125615_+\|diacylglycerol-kinase-family-protein	gnl\|CDD\|260134	cd14265, UDPK_IM_like, Integral membrane undecaprenol kinase and similar enzymes. This mostly bacterial family of homo-trimeric integral membrane enzymes, the products of the dgkA gene, catalyzes the ATP-dependent phosphorylation of undecaprenol to undecaprenyl phosphate. C55-isoprenyl (undecaprenyl) pyroposphate acts as a scaffold for the assembly of peptidoglycan components; undecaprenol kinase (UDPK) is involved in recycling undecaprenyl units for re-use in the peptidoglycan biosynthesis. UDPK does not participate in the de-novo biosynthesis of undecaprenyl phosphate. Gram-positive bacteria have a large pool of free undecaprenol, in contrast to gram-negative bacteria. UDPK may also play a role in a stress-induced pathway that affects the function of ribosomes. In Streptococcus mutans, UDPK has been shown to be required for biofilm formation, such as in the case of smooth surface dental caries. Members of the UDPK family have low activity as diacylglycerol kinases (DAGK), and many of them are annotated as DAGKs.	1.1023e-41
NZ_CP051167.1\|WP_168571810.1\|2126411_2127215_+\|MBL-fold-metallo-hydrolase	gnl\|CDD\|316044	pfam13483, Lactamase_B_3, Beta-lactamase superfamily domain. This family is part of the beta-lactamase superfamily and is related to pfam00753.	4.69293e-68
NZ_CP051167.1\|WP_168568786.1\|2132051_2132951_+\|tRNA-pseudouridine(55)-synthase-TruB	gnl\|CDD\|179469	PRK02755, truB, tRNA pseudouridine synthase B; Provisional.	3.16397e-158
NZ_CP051167.1\|WP_168571811.1\|2136923_2137112_+\|PspC-domain-containing-protein	gnl\|CDD\|377200	pfam04024, PspC, PspC domain. This family includes Phage shock protein C (PspC) that is thought to be a transcriptional regulator. The presumed domain is 60 amino acid residues in length.	3.68353e-25
NZ_CP051167.1\|WP_168568787.1\|2133271_2134306_-\|mechanosensitive-ion-channel-family-protein	gnl\|CDD\|366370	pfam00924, MS_channel, Mechanosensitive ion channel. Two members of this protein family of M. jannaschii have been functionally characterized. Both proteins form mechanosensitive (MS) ion channels upon reconstitution into liposomes and functional examination by the patch-clamp technique. Therefore this family are likely to also be MS channel proteins.	2.67776e-38
NZ_CP051167.1\|WP_168568781.1\|2124230_2124440_+\|DUF3285-domain-containing-protein	gnl\|CDD\|314535	pfam11688, DUF3285, Protein of unknown function (DUF3285). This family of proteins with unknown function appears to be restricted to Cyanobacteria.	7.09907e-27
NZ_CP051167.1\|WP_168568776.1\|2118835_2119618_-\|RNA-polymerase-sigma-factor-SigF	gnl\|CDD\|180965	PRK07408, PRK07408, RNA polymerase sigma factor SigF; Reviewed.	7.08254e-151
NZ_CP051167.1\|WP_168568785.1\|2130875_2131613_+\|class-I-SAM-dependent-methyltransferase	gnl\|CDD\|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	1.88057e-17
NZ_CP051167.1\|WP_168568783.1\|2125744_2126353_+\|aminodeoxychorismate/anthranilate-synthase-component-II	gnl\|CDD\|235552	PRK05670, PRK05670, anthranilate synthase component II; Provisional.	3.74513e-124
NZ_CP051167.1\|WP_168568784.1\|2129682_2130465_-\|uroporphyrinogen-III-C-methyltransferase	gnl\|CDD\|235711	PRK06136, PRK06136, uroporphyrinogen-III C-methyltransferase.	9.72087e-147
NZ_CP051167.1\|WP_168568789.1\|2134924_2136853_+\|S9-family-peptidase	gnl\|CDD\|224423	COG1506, DAP2, Dipeptidyl aminopeptidases/acylaminoacyl-peptidases [Amino acid transport and metabolism].	1.60714e-78

>NZ_CP051167.1|WP_168571810.1|2126411_2127215_+|MBL-fold-metallo-hydrolase
MNRRQLLKYASLGVLSAVGTGWPSMGQPGRAQSTSPSPSPTPASNALTVQWLGHTAFLFSGGGRRVLVNPFRNLGCTAGYRPPKVGADLVLISSRLLDEGATDGLPGSPRLLYEPGAYQLGSESIQGIRTDHDLEGGRRFGINVVWVWSQAGLRIVHLGGAAAPITMEQQILIGRPDLLLLPVGGGPKAYGPEAAKATMDRLNPRLVIPTHYLTEAAGQGCELVEVDRFLSLVDPAIVDRAGGDTLQLTRESLPETGTRVKVLSYRF
>NZ_CP051167.1|WP_168568783.1|2125744_2126353_+|aminodeoxychorismate/anthranilate-synthase-component-II
MIVVIDNYDSFTYNLVQYLGELGNDWPVASEIRVYRNDRLSVEELEQLQPSAIVISPGPGRPEDAGISLEIIEKLGPTIPILGVCLGHQCIGQVFGGKIVSAAELMHGKTSEVHHNDVGVFRGIENPMTATRYHSLVIDRNTCPPDLEITAWVEDGTIMGVRHRHYPHIQGVQFHPESILTQSGKQLLTNFLSQVKELSVAR
>NZ_CP051167.1|WP_168571809.1|2125159_2125615_+|diacylglycerol-kinase-family-protein
MSHEVPTPPTKRSGKSSPVDRQFSWKIANSLLISFKYAWQGITYAFGTQRNFRIHVAIGSLAVSLGVALSLTGLELAIISLTIGLVLTLELLNTAIESVVDLTVEQTYHELAKIAKDCAAGAVMVSSFAAITVAGLLIIPRLYGAIAALFF
>NZ_CP051167.1|WP_168568782.1|2124452_2124974_+|rRNA-maturation-RNase-YbeY
MIDRRIELELSVQQPFWESPGAASFPDPAIASETWESWFASWLALMRAELPSARGYELSVRLSDDGEIRQLNAGYRQQDKPTDVLAFAALEVDSPLAGPFESDDLLYLGDIAISVETAARQAIARGHGLTVELAWLAAHGLLHLLGWDHPDDDSLSRMLAQQETLLHAVGLEI
>NZ_CP051167.1|WP_168568781.1|2124230_2124440_+|DUF3285-domain-containing-protein
MNDSSTAPETADLENNPTPEAASAGEPPPSYVKLAMRNMVRKGGKSLKHFFLTATGLIALLVGLSYLTR
>NZ_CP051167.1|WP_168568780.1|2122789_2123918_+|peptide-chain-release-factor-2
MDLLEIKREIEMLSDRLGKTQEYLDLPALKAKIHDLEQLAAQPDFWDDQTHAQQTLQELNDLKSHLEQYAEWTSSLEDTKAILELLELESDEGLNQEAEQNLTRLARELDRWELQQLLSGPYDKNGAILSINAGAGGTDAQDWAEMLLRMYTRWGEAHGYKVHCMELSEGDEAGIKSATLELEGRYAYGYLRGEKGTHRLVRISPFNANGKRQTSFAGVEVMPILDDSIELEIPEKDLEITTTRSGGKGGQNVNKVETAVRIVHVPTGIAVRCTQERSQLQNKEKALAILKAKLLTVAQEQRAKEIAEIRGDMVEAAWGNQIRNYVFHPYQMVKDLRTGTETTAIGDVMDGELDEFVETYLRQDNQIGEFASASV
>NZ_CP051167.1|WP_168568779.1|2121856_2122582_+|hypothetical-protein
MSNTSNFQNAFQKARSQSLVGPNVIPKALPFLGGGLVLTALGTYGGLSVLTNSPNLFVTTFWGALILELILFFAVRGVAEKANNSVALPLLVTYSLLSGYTLAGIVSLALSTQGVGIEGIGIAALGCGVTFIAARQIGSNLGDEDGLALTQTVQLGIIALLVVLVAQLLLGFFGIYTPTWLEIGISGLGVLLFCGAAVVDFYILPRTYRDEQYLSAALSMYLTYINLFIFILRLLIAFNRD
>NZ_CP051167.1|WP_168568778.1|2120450_2121785_+|IS200/IS605-family-element-transposase-accessory-protein-TnpB
MSKAIVRTDKWGLQPSPEVRLHLAATVDEYRAYCKALSYVVMGHWPELVAAKSFCAAVEKLIHRTRKNPDPKYLYFGKRFYKFPSYLRRAAIKFVEGQVSSYLTRYREWQSGVRKRRDAKPPAFNVDAECYPALYKGQLVKFDVHLMVAWIKVWNGSDWVWAEVPIASKRHRHLIGSIKSPYLVVSQKRCHLAVPFGIVPPKWETDVVCAVDVGINTLATASIVCPDGTVLARKFIHPASDIDRRDKQTNIIRQKARKTKTLHRGFAKTPYRKAKGINANIARQVSRQIVNFALEHGASTIVFEDLKGWRPKGGKKRSNLKQRFHGWLHRRLVLLTQEKFQEVGGKTEYVYARGTSSWAFDGSGKVRRSKTQYELATFANGKRYNADLGASYNIAARYLAYKLKLTRRKDGQVAKGKSSCATPRMPVTLSLLWDWEAAYEREAS
>NZ_CP051167.1|WP_168568777.1|2119984_2120434_-|IS200/IS605-family-transposase
MERDFVTLKTRNHSAYRLCYHLVLSMKYRHKCLSAEMLNRLEVIFTDLLVKWGGELIEFGGEPDHVHLLFEVDPTIRLSDLVKNLKSVSARKMRQEFAEQLRPFYWKPYFWNRAYGLMTTVGQANIETLLKYIENQDDPRQLRPPLTSE
>NZ_CP051167.1|WP_168568776.1|2118835_2119618_-|RNA-polymerase-sigma-factor-SigF
MADQSSVRSRGMELLIAYHHNPSIQIRNQIVRLNVGLVRKIAHRVSHQCAEPYEDLEQIGYLGLIRAIERFDPTQGCAFSSFAVPYIRGEMLHFLRDKASTVRIPRRWRELQAQGQKVRESLTVSLGRPPKDLEIAQALDVSLSEWRESKLAHQNRTPLSLDATVAHQVDSTVTLGDTLLDTHYQTLQSLEEERQQLQGALNNLEEKTRWAIESVFFQEIPRKEVAQQIGVSPMTVTRRIKRGLGELMTLLKPSLAQVES
>NZ_CP051167.1|WP_168568784.1|2129682_2130465_-|uroporphyrinogen-III-C-methyltransferase
MNQSEQIRCVGKVYLVGAGPGDPGLLTLKGKTLLEYADVVVYDALVSPQILETINPKAERIDAGKRRGRHSLKQEETTRILIEKARTHAAVVRLKGGDPFVFGRGGEEMEDLIAAGVPVEVVPGVTAGIAAPAYAGIPLTHRHYSSSVTFVTGHEAAGKYRPEVNWSAIAHGSETIVIYMGIHNLPYITRELQKAGLSPETPIALIRWGTRIEQEELIGTIGSIVRQVEETGFEAPAIAAIGSVVKLHEIFGNSRPVVFA
>NZ_CP051167.1|WP_168568785.1|2130875_2131613_+|class-I-SAM-dependent-methyltransferase
MELDALLKLHCDLPQEGPGSDEATLDALRRLPPLPSSSRVFDLGCGPGRHTLVLARALDTRIVAVDLYKQFLVQLREAATDANLSDRIETRVGDMSQLDEPPESIDLIWSEAAIYTIGFERGLRYWYSLLKPTGFAVVSEVTWLDPTPPPEAIAFWEQEYPEMTDISSNLELAAQAGYKVFDHFVLNRAAWDAYYGPLRDRVRYWRSQPNLDENFLQVLDETEREIEVFDRYGDSFGYVFYLMQK
>NZ_CP051167.1|WP_168568786.1|2132051_2132951_+|tRNA-pseudouridine(55)-synthase-TruB
MQGFVNLNKPTGMTSHDCVARVRRLLRTKRVGHGGTLDPAATGVLPIAVGKATRLLPYLPTGKAYRGTVRFGVTTATDDLEGTVISQNPVPTLTRDAVEAVLGRFVGAIEQIPPAYSAIQVNGKRLYQLARAGEAVEVPARQVEIYRIALSEWRGGDYPEAVLDIECGPGTYIRAIARDLGEILATGGTLAALTRTQSCGFALADSVTFEEMETACDRGTFTPIAPDKALAHLSKVSLSPEFARRWCQGQRVPLPPASGNCPPPVCVDRDDGEFLGIAEITESEGDRRLVPKMVFLPEG
>NZ_CP051167.1|WP_168568787.1|2133271_2134306_-|mechanosensitive-ion-channel-family-protein
MIEASTLIKFLVPLFLILSGLIAGLIIEKRLIQKLKSIPQVRDYARYQTFIDSLHGIPFVIFFTAGIYTALIASQLSPEIRLFLSRIILTIILGALTLVISRLCIGFVRVYSQTSDSDLPLTSLFVNLTRLVIFTIGSLIILQSIGISITPLLTALGVGGISIGLALQTTLSNLFSGLNIIMSRKVNPGDYVKLETGEEGYVTDVTWRHTTIREIPNNLIVVPNAQLVSATFKNYSLPEREIIVLVEVGVAYGSDLENVEKVTLSVAEEVMREVVGGVPEFEPFLRFHTFGYFSINFTVYFGAKKYFDHLITRHEFIKRLHKRYQEEGIEIPFPIRPVYPQDPM
>NZ_CP051167.1|WP_168568788.1|2134652_2134793_+|ribbon-helix-helix-protein,-CopG-family
MARDELLQIRLTAQEKERLQAEADRRGVSMSEVIRDYIKRLPKQKA
>NZ_CP051167.1|WP_168568789.1|2134924_2136853_+|S9-family-peptidase
MTQRQIQAYGSWKSPISSDLIIAGTVGIGQLALDGETVYWLEMRPTEGGRYAIARRRPDGKTEDVTPPEFNVRTRVHEYGGGAYLVAEETVYFVNFSDQRLYRQSPGGDPEAITPDDGRRYADFDHDRPRQRLIAVREDHSSAGEPVNTIAAISLDGRSSTQVLVAGDDFYSSPRVSPDGSQLCWLSWNHPDMPWDATELWVASLDADGNLGDSQRVAGGHDESIFQPQWSEDGQLYFVGDRSGWWNLYTWDGQQVRAICPQTAEFGLPHWVFGMSTYGLISPEAIACSYSREGLSHLGRLNVKTGDLQEIQTPYTSIASLQVQGNRAVFIGGSASEPTAVVQLDLDTGTYKILRQSTTLDFDRAYLSTPKPIAFPTTESATAYGIFYPPQNPDYEAPEGELPPLLVKSHGGPTASASSTLSLGIQYWTSRGFAVLDVNYRGSTGYGRDYRLQLHGHWGIYDVDDCANGAKYLADRGLVDGDRLAISGGSAGGYTTLCALTFRDTFKAGASHYGVSDLEALAKDTHKFESRYLDKLIGPYPDRRDLYEQRSPIHHCDRLSCPVIFFQGLEDKIVPPNQAETMLEVLRGKGLPVAYVAFEGEQHGFRRGENIKRALDGEFYFYARVFGFDPADAIEPVAIENL
>NZ_CP051167.1|WP_168571811.1|2136923_2137112_+|PspC-domain-containing-protein
MNNKRLYRSQRNQQIAGVCSGVAQYFGVDPTVVRLAFVLFALMGGPGLVLYLIMWVVVPLEP
>NZ_CP051167.1|WP_168568790.1|2137457_2138468_+|hypothetical-protein
MKLMKSKLWRGCSLVLLAGSIAASIDRPQTASADVRIAPLQTAQLETGESGDRPTDTNRFQLLDRGIEPRQELSFSPAENSKEILSVVTNMDMNMSIAGRMIPAMDMPGMMMKMETVVDRVEDNGDIHLSFVYTESDVMDAANSPPMMVEAIRSELQKIVGMTGTMLVNKHGATKLANFDLPGNIDPNTQQLFDRTMSSIEEISTPLPSEAIGVGARWQIVNSPAVNGMKLEQIATYEIVELQDNQITLDIAVTQNADPQTPQLPGMPPDAKIDLKSYTGNGRGRVILQLDKMMPVRGSIAIDSNTQMEIGSKSSNSVEAMPVEMDMTMQMDMESL
>NZ_CP051167.1|WP_168571812.1|2138572_2139649_-|ferrochelatase
MGYGEVESYEDFANYNEQALNLLTAKFAPVPTWIYPPLAKLLALFDFHEWNHQHDNFISPHNAIFEKQREGIEKALQQRWGDRVEVFKAFNFCAPFLPEQVLAEIQQQGFQKLLIYPLLVVDSIFTSGIAVEQVNKALDRLADQDSGQSPIQSMRYIPSFYNEPDYIALMAQLVEETIAAELRGDYLPSEIGIVLMNHGCPHKAKGFTSGIRESEALYESVREQLIYRYPLISVGWLNHQTPLIEWTQPNAHLAAENLIQLGAKAIVFMPIGFATENHETLLDVHHIIHALEARHDRVRYVQMACVNEHPQFLQMAAEWAHPQIEALLAETEVSAVSASHSRTHARGHTHNHTHSHAH
>NZ_CP051167.1|WP_168568791.1|2139902_2141969_-|diguanylate-cyclase
MKGVKQELKGFCQWEWLSRYLPTLLSVGIGLVLSGVGFEAIARWQRSMQMADLEAKTQNVARAVETQIDAHLQGIWSIGDVLALGKGSFQPQGFETLARHFIARHSGVEALMWAPRIDRERRSDYERAMGERLGRAVTLSEGRSPAFPVSAIEPSTQRGFSLGLDLTTIAAFEDAIARSVQSQQAAVSFEPTPGNPYGSFAAIVPIYDADDELLGLAIALFDSGRLLKQAFKGIPLDEIDVVFSEPRRSPQIQWLTLYRSDLEQTYAEPEIQGKIAHLIRRDACSVPARCRYPVVIAGHEAIVQLLPKTTQSPFNAPLLAWIFLGAGLSLTAIVVAYLAEVQKRSAHLQHQIQDLSQANFELTRLNRIGDLLQACVTLEEAYETIPRLVEKLFPEQAGSLYILSASGNVLEAVSSWGEPTGSELVFGPDECWAIRSGRPHIFEKKHSGLACAHLRHPFPSMCLCIPMMAQGETLGLLYLSSRQRNGLSESKQELADNFAERLGLALANLKLREKLKNQSIRDPLTGLFNRRYLEESLERELYRATREQQGLGVILLDIDHFKQFNDTFGHDAGDTLLKELAMFLQGNIRQSDIACRYGGEEFVLIVPDASLDTIVDRAELLRQGVKHLHVQYHRESLGTISLSFGVACFPQNGKSASGLIEAADAALYEAKAQGRDRVAIASSGSTDL

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Crispr_ID: NZ_CP051167_12

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_12

2150242-2150357

Orphan

N:A

Consensus_repeat	Method
GCACCAGGAGCTTCTTCTCCAGAAGCGGCAGCTCCAGCACC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051167_12

>merge|NZ_CP051167|12|2150242-2150357|CRISPRCasFinder
GCACCAGGAGCTTCTTCTCCAGAAGCGGCAGCTCCAGCACCGGACGGGATGGTGACGCTTAGCGATCCAGGCATGGCACCAGGAGCTTCTTCTCCAGAAGCGGCAGCTCCAGCACC

>NZ_CP051167|12|11|2150242-2150357|CRISPRCasFinder
GCACCAGGAGCTTCTTCTCCAGAAGCGGCAGCTCCAGCACC	GGACGGGATGGTGACGCTTAGCGATCCAGGCATG
GCACCAGGAGCTTCTTCTCCAGAAGCGGCAGCTCCAGCACC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168571815.1\|2159203_2160121_-\|NAD(P)H-dependent-glycerol-3-phosphate-dehydrogenase	unknown	unknown	gnl\|CDD\|237771
NZ_CP051167.1\|WP_168568808.1\|2160147_2161026_-\|lipoyl-synthase	unknown	unknown	gnl\|CDD\|235493
NZ_CP051167.1\|WP_168568802.1\|2152670_2153606_-\|CHAD-domain-containing-protein	unknown	unknown	gnl\|CDD\|214880
NZ_CP051167.1\|WP_168568807.1\|2157318_2158578_-\|RNA-polymerase-sigma-factor-SigC	unknown	unknown	gnl\|CDD\|236067
NZ_CP051167.1\|WP_168568801.1\|2151956_2152487_-\|orange-carotenoid-protein	unknown	unknown	gnl\|CDD\|370323
NZ_CP051167.1\|WP_168568803.1\|2154061_2155183_+\|hybrid-sensor-histidine-kinase/response-regulator	unknown	unknown	gnl\|CDD\|223715
NZ_CP051167.1\|WP_168571813.1\|2145114_2145486_-\|response-regulator	unknown	unknown	gnl\|CDD\|381085
NZ_CP051167.1\|WP_168568797.1\|2146982_2147786_+\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|369777
NZ_CP051167.1\|WP_168568804.1\|2155330_2156461_+\|peptidoglycan-binding-protein	unknown	unknown	gnl\|CDD\|225943
NZ_CP051167.1\|WP_168568796.1\|2146561_2146720_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568800.1\|2149154_2149535_+\|cytochrome-c	unknown	unknown	gnl\|CDD\|365823
NZ_CP051167.1\|WP_168568794.1\|2144065_2144668_-\|chemotaxis-protein-CheC	unknown	unknown	gnl\|CDD\|381738
NZ_CP051167.1\|WP_168568799.1\|2148478_2148592_-\|cytochrome-b6-f-complex-subunit-PetG	unknown	unknown	gnl\|CDD\|179084
NZ_CP051167.1\|WP_168568809.1\|2161269_2161371_+\|twin-arginine-translocation-signal-domain-containing-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568793.1\|2142158_2144069_-\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|143635
NZ_CP051167.1\|WP_168568805.1\|2156489_2156945_-\|transcriptional-repressor	unknown	unknown	gnl\|CDD\|366663
NZ_CP051167.1\|WP_168568806.1\|2157079_2157289_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568798.1\|2147857_2148418_+\|16S-rRNA-(guanine(966)-N(2))-methyltransferase-RsmD	unknown	unknown	gnl\|CDD\|188022
NZ_CP051167.1\|WP_168568792.1\|2141967_2142120_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568795.1\|2145946_2146498_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168571815.1\|2159203_2160121_-\|NAD(P)H-dependent-glycerol-3-phosphate-dehydrogenase	gnl\|CDD\|237771	PRK14619, PRK14619, NAD(P)H-dependent glycerol-3-phosphate dehydrogenase; Provisional.	0
NZ_CP051167.1\|WP_168568808.1\|2160147_2161026_-\|lipoyl-synthase	gnl\|CDD\|235493	PRK05481, PRK05481, lipoyl synthase; Provisional.	0
NZ_CP051167.1\|WP_168568803.1\|2154061_2155183_+\|hybrid-sensor-histidine-kinase/response-regulator	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.78792e-52
NZ_CP051167.1\|WP_168568807.1\|2157318_2158578_-\|RNA-polymerase-sigma-factor-SigC	gnl\|CDD\|236067	PRK07598, PRK07598, RNA polymerase sigma factor SigC; Validated.	0
NZ_CP051167.1\|WP_168568801.1\|2151956_2152487_-\|orange-carotenoid-protein	gnl\|CDD\|370323	pfam09150, Carot_N, Orange carotenoid protein, N-terminal. Members of this family adopt an alpha-helical structure consisting of two four-helix bundles. They are predominantly found in prokaryotic orange carotenoid protein, and carotenoid binding proteins.	1.00951e-72
NZ_CP051167.1\|WP_168571813.1\|2145114_2145486_-\|response-regulator	gnl\|CDD\|381085	cd00156, REC, phosphoacceptor receiver (REC) domain of response regulators (RRs) and pseudo response regulators (PRRs). Two-component systems (TCSs) involving a sensor and a response regulator are used by bacteria to adapt to changing environments. Processes regulated by two-component systems in bacteria include sporulation, pathogenicity, virulence, chemotaxis, and membrane transport. Response regulators (RRs) share the common phosphoacceptor REC domain and different effector/output domains such as DNA, RNA, ligand-binding, protein-binding, or enzymatic domains. Response regulators regulate transcription, post-transcription or post-translation, or have functions such as methylesterases, adenylate or diguanylate cyclase, c-di-GMP-specific phosphodiesterases, histidine kinases, serine/threonine protein kinases, and protein phosphatases, depending on their output domains. The function of some output domains are still unknown. TCSs are found in all three domains of life - bacteria, archaea, and eukaryotes, however, the presence and abundance of particular RRs vary between the lineages. Archaea encode very few RRs with DNA-binding output domains; most are stand-alone REC domains. Among eukaryotes, TCSs are found primarily in protozoa, fungi, algae, and green plants. REC domains function as phosphorylation-mediated switches within RRs, but some also transfer phosphoryl groups in multistep phosphorelays.	8.55296e-30
NZ_CP051167.1\|WP_168568797.1\|2146982_2147786_+\|methyltransferase-domain-containing-protein	gnl\|CDD\|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	2.16782e-27
NZ_CP051167.1\|WP_168568804.1\|2155330_2156461_+\|peptidoglycan-binding-protein	gnl\|CDD\|225943	COG3409, COG3409, Putative peptidoglycan-binding domain-containing protein [Cell envelope biogenesis, outer membrane].	1.06927e-23
NZ_CP051167.1\|WP_168568800.1\|2149154_2149535_+\|cytochrome-c	gnl\|CDD\|365823	pfam00034, Cytochrom_C, Cytochrome c. The Pfam entry does not include all Prosite members. The cytochrome 556 and cytochrome c' families are not included. All these are now in a new clan together. The C-terminus of DUF989, pfam06181, has now been merged into this family.	2.2018e-11
NZ_CP051167.1\|WP_168568794.1\|2144065_2144668_-\|chemotaxis-protein-CheC	gnl\|CDD\|381738	cd17910, CheC_ClassII, chemotaxis protein CheC, Class II. This family contains class II CheC proteins found in proteobacteria, which diverge from class I CheCs in sequence conservation and lack critical well-conserved residues for CheD binding. These proteins are likely to be dedicated phosphatases. The class II cheC genes are not found in chemotaxis operons, but in operons containing more archetypical two-component signaling components, non-signaling operons, or as orphans. Thus, class II CheCs appear to be involved in non-chemotactic two component systems. Class II CheCs lack the first of the two phosphatase active sites of class I CheCs, and retain the second active site of class I CheCs.	5.1287e-69
NZ_CP051167.1\|WP_168568799.1\|2148478_2148592_-\|cytochrome-b6-f-complex-subunit-PetG	gnl\|CDD\|179084	PRK00665, petG, cytochrome b6-f complex subunit PetG; Reviewed.	2.38908e-16
NZ_CP051167.1\|WP_168568793.1\|2142158_2144069_-\|diguanylate-cyclase	gnl\|CDD\|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	1.29731e-61
NZ_CP051167.1\|WP_168568805.1\|2156489_2156945_-\|transcriptional-repressor	gnl\|CDD\|366663	pfam01475, FUR, Ferric uptake regulator family. This family includes metal ion uptake regulator proteins, that bind to the operator DNA and controls transcription of metal ion-responsive genes. This family is also known as the FUR family.	1.15648e-48
NZ_CP051167.1\|WP_168568798.1\|2147857_2148418_+\|16S-rRNA-(guanine(966)-N(2))-methyltransferase-RsmD	gnl\|CDD\|188022	TIGR00095, Putative_methylase_yhhF., 16S rRNA (guanine(966)-N(2))-methyltransferase RsmD. This model represents a family of uncharacterized bacterial proteins. Members are present in nearly every complete bacterial genome, always in a single copy. PSI-BLAST analysis shows homology to several families of SAM-dependent methyltransferases, including ribosomal RNA adenine dimethylases. [Protein synthesis, tRNA and rRNA base modification].	2.2558e-61
NZ_CP051167.1\|WP_168568802.1\|2152670_2153606_-\|CHAD-domain-containing-protein	gnl\|CDD\|214880	smart00880, CHAD, The CHAD domain is an alpha-helical domain functionally associated with some members of the adenylate cyclase family. It has conserved histidines that may chelate metals.	1.51107e-23

>NZ_CP051167.1|WP_168568800.1|2149154_2149535_+|cytochrome-c
MNHQVAKSEVTSSSQKVWAIAVTIVLAILISVAIAYQFQISDPYTKTVLSLSGDPIRGHAIFQMNCAGCHGSRRGTQVGPSLTDVSQRKSRVGLIEQVTSGKTPPMPQFQPSPQAMADLLSYLESL
>NZ_CP051167.1|WP_168568799.1|2148478_2148592_-|cytochrome-b6-f-complex-subunit-PetG
MVEPLLSGIVLGLITVTLAGLFFAAYQQYKRGNQFDL
>NZ_CP051167.1|WP_168568798.1|2147857_2148418_+|16S-rRNA-(guanine(966)-N(2))-methyltransferase-RsmD
MSLRIYGNRLVKTLPGQQTRPTAARVREALFNIWQGAIVGCHWLDLCAGAGSMSAEALCRGADTVVAIEQSGRACQLIRENLAKYAREEQQFYVYRGDVLKQLPKLGARQYDRIYFDPPYHGELYSGVLDAIARYDLLAADGELAVEHDPNRPPMATVSHLKICRQKVYGNCAITFYRLETNDATA
>NZ_CP051167.1|WP_168568797.1|2146982_2147786_+|methyltransferase-domain-containing-protein
MQGGTHSFLSNPQAPAWNAKLYDAKHIFVSEYATDLLNLLNPKLDDRIFDLGCGTGHLTARIAASGARLVGGDSSPAMLDRARALYPALEFILVDGEHLPFDNEFDAVFSNAALHWMKQPEKVAAGIARSLKPGGRFVAEFGGKGNIAQMRRALYLALEKEGLSASQIDSPWYFPSIGEYTSILEKYGLCVTFAVLFDRPTSLSEGDRGMRNWFTMFANSFFRELSDTQRDRVLSDIDNQLRPTLYENGTWIADYKRLRVVAVKPSS
>NZ_CP051167.1|WP_168568796.1|2146561_2146720_-|hypothetical-protein
MKSPLVILAWSVLLLSVSQLMLAFVKTVELERSPAISQEAAQFSRAIAVRDN
>NZ_CP051167.1|WP_168568795.1|2145946_2146498_+|hypothetical-protein
MRLLICPGIHDPQLTRQFLDDLTGDERWSDRHLECLVFPAWDYPAYSALHILHFLDRETARNDDRAIAWIAFSAGVVGAIGAAWGWQALGGTVKAAIALDGWGVPLYGNFPIYRLSHDRFTHWSSALLGPGRASFYADPAVDHLQLWRSPATVAGYAVENDDCTAKERRTTALDFLLEILLEF
>NZ_CP051167.1|WP_168571813.1|2145114_2145486_-|response-regulator
MALILIVEDAMFSRKMIRKTLQKQGYETLEAKNGKEGLELVREVNPDCILLDLLMPEIDGWEFLKILRAEGYKTPTIVITADIQETSRQQCLELGAQAVLNKPPQAQVMQDAIEAVLATPSEG
>NZ_CP051167.1|WP_168568794.1|2144065_2144668_-|chemotaxis-protein-CheC
MTPTVEQIDALQEMINIGVGRAASVLNEMLESHISLQVPYIKIFSPSELTEELEHRLGPIQLSAVRLMFTGSLSGNAQLVFPTDSASKLVSLLTQDELDSLDLDSLKIGTLSEVGNIVINGVMGSISNLLGQHFNYSLPIYIEDTVDHLLTWSEFDPNLVILLAQARFSVESMHIQGDIILIFTVSSFDSLIDSLQLQYE
>NZ_CP051167.1|WP_168568793.1|2142158_2144069_-|diguanylate-cyclase
MNLLIMDEVERVAQAFFILDRIPFGSCILREDLVVVFWNSRLEEWTKIPRHTILGRSIVDFFPHLEKPKYKTRLKPIFQGGPPTIFSSQLHKHIIPAKLPNGDLRIQHTTVTSIPRFEGDSYYAILAIQDVTDLTERIQDYRQMRDRALEEIKERQQAQEALYQKTAEFEAIFKSIPDAVVFANLSGEMILLNPAFSKLFGYSSEEMLGQPISVLQADYSNSEQNCYGKGKYSQARDGAIASDLVQPYEVEYQRKNRDIFVGETIDSVVKDGEGKTLGLLRIVRDITERKQAAGALESANQKLKDWVTELENRHRETLILREMSDLLQACLTVEEAYAVIARSVQLLFPNLSGALFILDDSKKLVEAVAQWGDVETTETVFLPQECWALRRGREHFVCDNRGGLPCKHVLNDGLEYSCTPLMAQGKGLGTLYLCSEKSGEFTASKQLLTLTVTEQISLSLANLTLRETLKQQSIRDPLTGLYNRRYLQECLGREIHRARNQNVGVGVIMLDVDRFKQFNDSFGHEAGDEILKKLASFLQENNSEADIACRYGGEEFTVILPQSSLEQTQEKAHLLREGVRLVQVRYQQQLLGPLTISVGVANFPEHGQSGDALLRAADTALYRAKREGRDRTVVAE
>NZ_CP051167.1|WP_168568792.1|2141967_2142120_+|hypothetical-protein
MRTLFSSEKTGKNIVDVDGYPAMIALHPRRDRQQRSPPQSMQVITTFNRA
>NZ_CP051167.1|WP_168568801.1|2151956_2152487_-|orange-carotenoid-protein
MTAINTTGNSQIRSEDTKKIVERFEGLKTDDQLALLYWIYEKMGDSITPAAPTATDPQIAPLLLDNFFKLSDDEQLQVMRDLVERKDTQYSHAYGALTANNQLLVWYAWAIAMGDTVVDLPENYSADGAVKDILKQVENAEFQDQISILREIAANMGYTDIGEVPSQEQTGKTPSL
>NZ_CP051167.1|WP_168568802.1|2152670_2153606_-|CHAD-domain-containing-protein
MAYRIQEQETIDRGIKRIVGDEIELAIADLRGHTHLAQEEAIHDARKRLKKLRAVARLVRFGIGDEAYRRENQTWRDAGRLLSDVRDASVYVETLDKLKSAYANYIAADAFSTTRSSLVDRRDAILKQHLGEDNKMEQAAAKIEQSRTQVEEWNLGDRDWEAIAPGFQRIYKQGRKALQHAFENRSIENFHDWRKRVKDFWYHLRILESIWPSLMNQMQTEAKQLSDYLGDDHDLAVLRQLLVEYPKLCPDREEFEALIASIDLRRNQLQRSAKVLGDRLYAEKASAFVDRLGHYWYTWKAEQSEAIGDWN
>NZ_CP051167.1|WP_168568803.1|2154061_2155183_+|hybrid-sensor-histidine-kinase/response-regulator
MSHPPLSPNSKTADRILVVDDSPDNVLLVTTILEEEGYETSTAESGYSALEAIEQSPPDLVLLDIMMPGMDGYEVTRRLRSNADLPFIPILLITAHDRPSVVQGLDVGADDFIRKPVEIDELLARVRSLLRLKHSVDERDEIARQREDFVSRLTHDLRTPLVAADRMLGLLGQGALGAVTPEMQEAFDTMQRSNENLLKMVNTLLEVYRYEAARKRLTFTEVNLLQLIEELCAELEPMAQAQAIDLKIDDRYLSPENGFAETNIRGDRLELWRLFTNLIGNAIKFTEAGSVEITLKPESGAIAIAVEDTGPGIEPAEQANLFERFRSGNHKRSGSGLGLHLCRRIAEAHSGTIAVRSQVGKGSVFTVTLPILN
>NZ_CP051167.1|WP_168568804.1|2155330_2156461_+|peptidoglycan-binding-protein
METLAYIELARAYESQGDRDLPKATPRDRHFVWLCCSMPQLLGWSVLALLLAIAAPVPPTAAQTVLFQQGDSGPSVRSIQQRLKSFGYFNTDVTDYYGPITEAAVIEFQRANGLPVTGIVDSQTLQAMGRMAQRSAPVQSFAATPAQGFGTVTAVSSGNEVLRVGDRGVAVSALQQQLQQLGYFAGPVTGEFDYDTETAVIRFQQNNNLRADGLVGSNTRTALASQPQPAPTSQGFVPRGNTSGEIRYGDRGSQVRSLQQRLAIAGFPPSRIDGIFGDDTEISLKEFQQTYGLPPSGVADATTRRSLDRKLYVVVVPQFRQGTLEAVRQIFPDAFAADSRLGDYVHVGSSLRREIAEERTKLLRSQGFVDARVAYF
>NZ_CP051167.1|WP_168568805.1|2156489_2156945_-|transcriptional-repressor
MSAYTASSLKAELNERGWRLTPQRETILQVFQNLPKNEHLSAEDLYTLLQNQGENISLSTIYRTLKLLSRMGVLRELELAEGHKHYEINKPYPHHHHHLICVRCNKTIEFKSDSILKVGTKTAKKEGYHLLDCQLTIHAICPRCQRALLPL
>NZ_CP051167.1|WP_168568806.1|2157079_2157289_+|hypothetical-protein
MRTIRRSLAKSRTWGRLADRGGANGGKNGVDVKFYNIDRLAGADEIGLDAIARAVKQIVFKAIGAKVLI
>NZ_CP051167.1|WP_168568807.1|2157318_2158578_-|RNA-polymerase-sigma-factor-SigC
MPGISFNPNTEDDKRVNAQEFDDRGIASESDDEEAYAPIDVELDVDDADSATLVNKPSRRTTDLVRLYLQEIGRVRLLGRDEEVAEAQKVQRYMQLKELRDEAATDDNPELKRYVHLIETRDRLSSQLGLRPSLERWASESGIDVTELKPSLAAGKRKWAELAGLVLEELEKIQTEGVGAKEHMIKANLRLVVSVAKKYQNRGLELLDLIQEGTLGLERAVEKFDPTRGYRFSTYAYWWIRQGITRAIATQSRTIRLPVHITEKLNKIKKAQRKLSQEKGRTPTIDDIAEELEMTPANVREVLLRVPRSVSLETKVGKEKDTELGDLLETDDISPEEILMREALQRDLQHLLADLTTRERDVIRMRFGLGDGHPYSLAEIGRALDLSRERVRQIEAKALQKLRQPKRRNRVRDYLEALS
>NZ_CP051167.1|WP_168571815.1|2159203_2160121_-|NAD(P)H-dependent-glycerol-3-phosphate-dehydrogenase
MAPTRLAVIGAGMWGSTLGQLAAHNGHHVSLWSRHGDRSLAETVADAEILLSAVSMKGVRPVASQVRDLPIRPDAILVTATKGLDPETTCTPSTIWQDAVGDRPVVVLAGPNLSKEIQQGLPAATVVASTDFGAAERVQGIFSSMDFRVYTNRDPLGVELGGTLKNVMAIAAGVCDGLQLGTNAKAALLTRGLAEMIRIGSDWGAQVETFYGLSGLGDLLATCNSPLSRNYQVGYQLARDRGLPEILADLEGTAEGVNTTAVLLDRARRRDISMPISYQVGLLLDGSITPKAALEALMGRESKPE
>NZ_CP051167.1|WP_168568808.1|2160147_2161026_-|lipoyl-synthase
MSVKPDWLRVKAPQWERVGNVKEILRDLKLNTVCEEASCPNIGECFHNGTATFLIMGPACTRACPYCDIDFDKTPRSLDPEEPANLAEAVRRMRLNHVVVTSVNRDDLPDGGATQFARCIEAIRAASPGTTIEVLIPDLCGNWDALETILKAGPEVLNHNTETVERLYRRVRPQGNYERSLELLRRSRAIAPWVYTKSGIMLGLGESEAEIRQVMADLRRVDCDILTMGQYLQPTPKHLPIAEWVAPETFEQWQTLGESMGFLQVVASPLTRSSYHAEQVRALMERYPRSRS
>NZ_CP051167.1|WP_168568809.1|2161269_2161371_+|twin-arginine-translocation-signal-domain-containing-protein
MFSRRQFLQGSFGTMGAIAPALSPVPFATLDNF

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Crispr_ID: NZ_CP051167_13

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_13

2208642-2208794

TypeV

N:A

Consensus_repeat	Method
GATCCCCTTGAAATTGGGCTTCGAGGCGGGAAATCGTGGCTTGTTGG	PILER-CR

2 spacers

cas14j,c2c9_V-U4

The CRISPR arrays of NZ_CP051167_13

>merge|NZ_CP051167|13|2208642-2208794|PILER-CR
TCCCCTTGAAATTGGGCTTCGAGGCGGGCAATTTGAGCGTTTTGGGCGACGCGATCTTCTTGTAATTGGGCTTCGAGACGGGAAATGGTGGCTTGTTGGGCGCTCAGATCCCCTTGAAGTTGGGCTTCGAGGCGGGAGATCGTGGCTTGTTGG

>NZ_CP051167|13|9|2208642-2208794|PILER-CR
TCCCCTTGAAATTGGGCTTCGAGGCGGGCAATTTGAGCGTTTTGGGCG	ACGCGATCTTCTTGTAATTG
GGCTTCGAGACGGGAAATGGTGGCTTGTTGGGCGCTCAGATCCCCTTG	AAGTTG
GGCTTCGAGGCGGGAGATCGTGGCTTGTTGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168568855.1\|2216829_2217036_-\|glycogen-debranching-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568841.1\|2196769_2197834_-\|NTP-transferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|223906
NZ_CP051167.1\|WP_168571818.1\|2196179_2196620_-\|cupin-domain-containing-protein	unknown	unknown	gnl\|CDD\|380343
NZ_CP051167.1\|WP_168568848.1\|2206382_2207543_-\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|130253
NZ_CP051167.1\|WP_168568844.1\|2200064_2201864_-\|peptidase-S8	unknown	unknown	gnl\|CDD\|173810
NZ_CP051167.1\|WP_168568851.1\|2211051_2211252_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568847.1\|2205412_2206126_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|274374
NZ_CP051167.1\|WP_168568859.1\|2221465_2221882_+\|SCP-2-sterol-transfer-family-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568853.1\|2214742_2215642_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568843.1\|2199843_2200068_-\|cytochrome-c-maturation-protein-CcmE	unknown	unknown	gnl\|CDD\|376989
NZ_CP051167.1\|WP_168568852.1\|2213349_2214576_-\|IS200/IS605-family-element-transposase-accessory-protein-TnpB	cas14j	-	gnl\|CDD\|223747
NZ_CP051167.1\|WP_168568850.1\|2209632_2210898_-\|aspartate-aminotransferase-family-protein	unknown	unknown	gnl\|CDD\|235056
NZ_CP051167.1\|WP_168568842.1\|2198299_2199622_+\|LCP-family-protein	unknown	unknown	gnl\|CDD\|224235
NZ_CP051167.1\|WP_168568845.1\|2201891_2202155_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168568846.1\|2202196_2203159_+\|RDD-family-protein	unknown	unknown	gnl\|CDD\|377640
NZ_CP051167.1\|WP_168568854.1\|2215727_2216804_+\|potassium-channel-protein	unknown	unknown	gnl\|CDD\|367001
NZ_CP051167.1\|WP_168568857.1\|2218983_2219349_-\|DUF1818-family-protein	unknown	unknown	gnl\|CDD\|370153
NZ_CP051167.1\|WP_168571819.1\|2203189_2203966_-\|HAD-IIB-family-hydrolase	unknown	unknown	gnl\|CDD\|273651
NZ_CP051167.1\|WP_168568858.1\|2219366_2220581_-\|IS200/IS605-family-element-transposase-accessory-protein-TnpB	c2c9_V-U4	-	gnl\|CDD\|223747
NZ_CP051167.1\|WP_168568856.1\|2217492_2218863_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168568841.1\|2196769_2197834_-\|NTP-transferase-domain-containing-protein	gnl\|CDD\|223906	COG0836, {ManC}, Mannose-1-phosphate guanylyltransferase [Cell envelope biogenesis, outer membrane].	2.06612e-148
NZ_CP051167.1\|WP_168568852.1\|2213349_2214576_-\|IS200/IS605-family-element-transposase-accessory-protein-TnpB	gnl\|CDD\|223747	COG0675, COG0675, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	3.50957e-52
NZ_CP051167.1\|WP_168571819.1\|2203189_2203966_-\|HAD-IIB-family-hydrolase	gnl\|CDD\|273651	TIGR01484, Putative_mannosyl-3-phosphoglycerate_phosphatase, HAD-superfamily hydrolase, subfamily IIB. This subfamily falls within the Haloacid Dehalogenase (HAD) superfamily of aspartate-nucleophile hydrolases. The Class II subfamilies are characterized by a domain that is located between the second and third conserved catalytic motifs of the superfamily domain. The IIB subfamily is distinguished from the IIA subfamily (TIGR01460) by homology and the predicted secondary structure of this domain by PSI-PRED. The IIB subfamily's Class II domain has the following predicted structure: Helix-Sheet-Sheet-(Helix or Sheet)-Helix-Sheet-(variable)-Helix-Sheet-Sheet. The IIB subfamily consists of Trehalose-6-phosphatase (TIGR00685), plant and cyanobacterial Sucrose-phosphatase and a closely related group of bacterial and archaeal sequences, eukaryotic phosphomannomutase (pfam03332), a large subfamily ("Cof-like hydrolases", TIGR00099) containing many closely related bacterial sequences, a hypothetical equivalog containing the E. coli YedP protein, as well as two small clusters containing OMNI\|TC0379 and OMNI\|SA2196 whose relationship to the other groups is unclear. [Unknown function, Enzymes of unknown specificity].	1.60452e-23
NZ_CP051167.1\|WP_168568848.1\|2206382_2207543_-\|FtsX-like-permease-family-protein	gnl\|CDD\|130253	TIGR01185, membrane_spanning_subunit, DevC protein. This model describes a predicted membrane subunit, DevC, of an ABC transporter known so far from two species of cyanobacteria. Some experimental data from mutational analysis suggest that this protein along with DevA and DevB encoded in the same operon may be involved in the transport/export of glycolipids. [Transport and binding proteins, Other].	0
NZ_CP051167.1\|WP_168568844.1\|2200064_2201864_-\|peptidase-S8	gnl\|CDD\|173810	cd07484, Peptidases_S8_Thermitase_like, Peptidase S8 family domain in Thermitase-like proteins. Thermitase is a non-specific, trypsin-related serine protease with a very high specific activity. It contains a subtilisin like domain. The tertiary structure of thermitase is similar to that of subtilisin BPN'. It contains a Asp/His/Ser catalytic triad. Members of the peptidases S8 (subtilisin and kexin) and S53 (sedolisin) clan include endopeptidases and exopeptidases. The S8 family has an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure and are not homologous to trypsin. Serine acts as a nucleophile, aspartate as an electrophile, and histidine as a base. The S53 family contains a catalytic triad Glu/Asp/Ser with an additional acidic residue Asp in the oxyanion hole, similar to that of subtilisin. The serine residue here is the nucleophilic equivalent of the serine residue in the S8 family, while glutamic acid has the same role here as the histidine base. However, the aspartic acid residue that acts as an electrophile is quite different. In S53 the it follows glutamic acid, while in S8 it precedes histidine. The stability of these enzymes may be enhanced by calcium, some members have been shown to bind up to 4 ions via binding sites with different affinity. There is a great diversity in the characteristics of their members: some contain disulfide bonds, some are intracellular while others are extracellular, some function at extreme temperatures, and others at high or low pH values.	7.33071e-135
NZ_CP051167.1\|WP_168568843.1\|2199843_2200068_-\|cytochrome-c-maturation-protein-CcmE	gnl\|CDD\|376989	pfam03100, CcmE, CcmE. CcmE is the product of one of a cluster of Ccm genes that are necessary for cytochrome c biosynthesis in eubacteria. Expression of these proteins is induced when the organisms are grown under anaerobic conditions with nitrate or nitrite as the final electron acceptor.	0.00368663
NZ_CP051167.1\|WP_168568854.1\|2215727_2216804_+\|potassium-channel-protein	gnl\|CDD\|367001	pfam02254, TrkA_N, TrkA-N domain. This domain is found in a wide variety of proteins. These protein include potassium channels, phosphoesterases, and various other transporters. This domain binds to NAD.	2.79929e-33
NZ_CP051167.1\|WP_168568850.1\|2209632_2210898_-\|aspartate-aminotransferase-family-protein	gnl\|CDD\|235056	PRK02627, PRK02627, acetylornithine aminotransferase; Provisional.	0
NZ_CP051167.1\|WP_168568842.1\|2198299_2199622_+\|LCP-family-protein	gnl\|CDD\|224235	COG1316, LytR, Transcriptional regulator [Transcription].	2.71681e-61
NZ_CP051167.1\|WP_168568847.1\|2205412_2206126_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|274374	TIGR02982, heterocyst_DevA, ABC exporter ATP-binding subunit, DevA family. Members of this protein family are found mostly in the Cyanobacteria, but also in the Planctomycetes. Cyanobacterial examples are involved in heterocyst formation, by which some fraction of members of the colony undergo a developmental change and become capable of nitrogen fixation. The DevBCA proteins are thought export of either heterocyst-specific glycolipids or an enzyme essential for formation of the laminated layer found in heterocysts.	3.25464e-133
NZ_CP051167.1\|WP_168568846.1\|2202196_2203159_+\|RDD-family-protein	gnl\|CDD\|377640	pfam06271, RDD, RDD family. This family of proteins contain three highly conserved amino acids: one arginine and two aspartates, hence the name of RDD family. This region contains two predicted transmembrane regions. The arginine occurs at the N-terminus of the first helix and the first aspartate occurs in the middle of this helix. The molecular function of this region is unknown. However this region may be involved in transport of an as yet unknown set of ligands (Bateman A pers. obs.).	2.38576e-15
NZ_CP051167.1\|WP_168568857.1\|2218983_2219349_-\|DUF1818-family-protein	gnl\|CDD\|370153	pfam08848, DUF1818, Domain of unknown function (DUF1818). This presumed domain is found in a small family of cyanobacterial protein. These proteins are functionally uncharacterized.	1.10453e-65
NZ_CP051167.1\|WP_168571818.1\|2196179_2196620_-\|cupin-domain-containing-protein	gnl\|CDD\|380343	cd02213, cupin_PMI_typeII_C, Phosphomannose isomerase type II, C-terminal cupin domain. This family includes the C-terminal cupin domain of mannose-6-phosphate isomerases (MPIs) which have been classified broadly into two groups, type I and type II, based on domain organization. This family contains type II phosphomannose isomerase (also known as PMI-GDP, phosphomannose isomerase/GDP-D-mannose pyrophosphorylase), a bifunctional enzyme with two domains that catalyze the first and third steps in the GDP-mannose pathway in which fructose 6-phosphate is converted to GDP-D-mannose. The N-terminal domain catalyzes the first and rate-limiting step, the isomerization from D-fructose-6-phosphate to D-mannose-6-phosphate, while the C-terminal cupin domain (represented in this alignment model) converts mannose 1-phosphate to GDP-D-mannose in the final step of the reaction. Although these two domains occur together in one protein in most organisms, they occur as separate proteins in certain cyanobacterial organisms. Also, although type I and type II MPIs have no overall sequence similarity, they share a conserved catalytic motif.	3.43486e-49
NZ_CP051167.1\|WP_168568858.1\|2219366_2220581_-\|IS200/IS605-family-element-transposase-accessory-protein-TnpB	gnl\|CDD\|223747	COG0675, COG0675, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	1.08017e-45
NZ_CP051167.1\|WP_168568856.1\|2217492_2218863_-\|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.	1.37815e-25

>NZ_CP051167.1|WP_168568848.1|2206382_2207543_-|FtsX-like-permease-family-protein
MFRHKIPLAWCQLTREKSRLFVALAGISFANTLMFMQLGFRDALFDSSTRMHQNLNSDLVLIDPKSEALIAMQSFSWRRLYQVLAFEEVESIEPLYLGLINWKNPVQKNDRSILVMGFNPNKAALTMPEVNQHLDKIKLQDVVLFDRDSRPEFGPIPDLLAEKGSVETEVGMRRIQVRGLFSMGASFAADGNIITSDLNFIRLFEERDYGQIDVGLIQLKPGADPEKVRQKIDDYLPEDVRVLTHQGFIKFEQDYWATSTAIGFIFGLGVAMGFIVGIVIVYQILYTDVSDHLAEYATLKAMGYRDLYFLSVVFQEALILAILGYFPGFSLCSFFLYSLTQNATQLPVYMTVSRALFVFCLTLIMCAISGAIAVRKLRAADPADIF
>NZ_CP051167.1|WP_168568847.1|2205412_2206126_-|ATP-binding-cassette-domain-containing-protein
MKPFTSPVVNIKKLDHYFGQGDLRKQILFNIHLKIHPGEIVLMMGPSGSGKTTLLTLIGALRSPQNGSIEVLGNQLCDAPTERLVSVRRQIGYIFQGHNLLHSLTARQNVQMSLQLHADSLTDKELSERTATMLEAVGLGDRIDYYPEKLSGGQKQRVAIARALVSHPQLILADEPTAALDSKSGRDIVEIMQHLAKEQQTAILLVTHDHRILDVGDRIVRMEDGRLMRAEAIAALP
>NZ_CP051167.1|WP_168571819.1|2203189_2203966_-|HAD-IIB-family-hydrolase
MMSCLPLSEAIAQSRLQSVRLVATDMDGTLTCNGQLSGELLEVLEALRDRAIATLIVTGRSAGWVNGLSQLLPIAGAIAENGGIFYAANGESTLLTPIVDLPSHRQQLAAVFAELQRQFPDLCESSDNPFRLTDWTFDVQGLTTRALHSLKLRCRELGWDFTYSSVQCHIRPLGQDKAKGLLSVLSRYFPDHSPDCVVTVGDSPNDESLFDPHYFQLSVGVANVLDYTTRLTHQPAYVTGQPEGWGFCELARALVASD
>NZ_CP051167.1|WP_168568846.1|2202196_2203159_+|RDD-family-protein
MTSRRSQSFLDNLLRRILAGLIDYLLLISICWFGLGLQFNIGLTGLFADSQVVTINEPRNLFVIYLILVAYFSLGESFLGLTLGKFIFQAEVVTVRGHRPSLVQAALRNLFKPFDLLLLLSPILLSPKYQTLGDRFAKTLVIKRNAAVPTIPSNKYSLSPQKIVGWILLAVAIVNLTIWFYFASNYFPETKATARATNTYFMRLEKGFEIDNLESAYTTSSSRLQAEETLESFQQRLLGNPGLQFLLENRKDINFYRWEFKEDMAMLFGEIDKEFKITVVLDRENQQWKFLSGSVEPIENPQDLWNKPNEIPAGEQESVD
>NZ_CP051167.1|WP_168568845.1|2201891_2202155_-|hypothetical-protein
MVGRGVGAGEREDEGQQRQGKSTRASKWRSRQIAVVADPPGGAKAQNRAIALPSVREIILTHRGRPAIATDPAEIVPTDWSWVELWW
>NZ_CP051167.1|WP_168568844.1|2200064_2201864_-|peptidase-S8
MKKIFLLALFLVGLSWALFNFKGLANQGTFDAIVLDFREDLAAGQVERQLDQLGDRYGVKARLNSEFSREDNFYIVEGDRQLLKTLKKSELSKYTEYIEPDYQYKALTIPNDPLYGQQWNFRSINLEKAWENTKGNGITVAAIDTGVSKVPDLKDTQFVKGYDFVNDRELADDDNGHGTHVAGTIAQTTNNNYGVAGIAYEAKIMPLKVLSAGGGGNIGDIAEAIKFAANNGADVINMSLGGAGESQAMKEAIAYAHEKGVVVVAAAGNENRNSASYPARYTHVIGVAAIDSTGQKAPYSNFGAGVDISAPGGDTSKGESGGILQNTIAIDPDTRRPTSVFKAFQGTSMAAPHVAGVAALVKASGVENPDEVAEILKQSARVIKDDPLNHFGAGQLDAANAVQLAMHGKIDFRDFFRWLRDNGYLNPGFWIDGGVYTLVPKLLMMVGSYLLAWLLKTYFPFGWTWSMASGLIFGSSGLFVLRGFYIFDLPQWPMRVMGSSLPELGTAIQGSSALNPIFASVLIPGILIVLLLGHPQWKNFAIGTTLGVASCLAISAVLVPGPMLLWLGSGLGARAFLLVNAFLCFGLARLALKGEEKFA
>NZ_CP051167.1|WP_168568843.1|2199843_2200068_-|cytochrome-c-maturation-protein-CcmE
MSVSLTGTIERREMGTGAWALVADDGQTYEIYEGAPSDLLKPGQKVKVNGRIRDDVMTLAAIGPVLQVDGFELN
>NZ_CP051167.1|WP_168568842.1|2198299_2199622_+|LCP-family-protein
MPPEPLSVKLARLVFWSFTFLLMTTVAATVGGVLALIDPKNALTPQQLQARQAAEKLKAIAPNRDSMGFPRFELARPMTLLVMGVDPPLDAPDDPEAVFSGRSDTLLLVRLDPDRESISLLSVPRDTRVRLGDRGYAKINEANYLGGIPLTSEAISDLLDVEIDRYIRIGTGAFRELVDLLGGVEVFVPYPMSYTDRTQQLKIELKPGWQTLNGRQSEHFARFRNDAYGDIGRIQRQHLLVEALQTRLSDPSVLPQVSKVVRVMQKYINTNLSLEELLAAVKMGLGRSPESLQMVMLPGKISDGHDSDRSYWIVDRQGRDRVMAQYFGNGDETEGRSQPDQRALKRLDIAVQNASGNPQIARKLLHELQRQGFKNVYAIEDWPDRQPHSQIIVQKGDLESAKTLQTLLKFPRLETSSTGYLDSDLTLRIGEDVERGDFRF
>NZ_CP051167.1|WP_168568841.1|2196769_2197834_-|NTP-transferase-domain-containing-protein
MKSSMIPVILAGGKGERFWPLSRRARPKQFLCLDRTGKSLLQATADRLLDVAGGWQGLWVITSAELSDGVREQLPELPPENLLAEPQGRDTAPAVAWTTLEIAKRHGDDALIGFFPADHWIGDREGFKNTLEAASQLANSQRAIVTLGIEPTYPSSGYGYIEQGQGAGTYAGISAYRVNRFTEKPDRETAETFIETGKYTWNSGMFIFRAGVVIDELRAYAPEILDPIAERGVAAYADLPKKSIDYALMEKTHLTYVLPADFGWDDLGDWNALERLLKDDDCPNVEVARHLGLDTKGSIFYASNPEEAIVTIGLEDVVVVRDGNVTLIVKKERTQDIKKVLQSLKERPEYQSEL
>NZ_CP051167.1|WP_168571818.1|2196179_2196620_-|cupin-domain-containing-protein
MSETTTPTQNATQTPQEEKEAARYPETSETQERYWGTVTVLETGQRYRISRLEIKPGHRIMTQIHYHRSEHWIVVSGTAKVICGDDESLVIQNQSTYVPPCTAHRVENPGVIPLVLIEVQNGEFLGDEDTVRLADDAIGHGDRQPS
>NZ_CP051167.1|WP_168568850.1|2209632_2210898_-|aspartate-aminotransferase-family-protein
MSPESVLDNPAVENTPFDADEFDRVVMKTYGRFAIALERGRGCRVWDSDGKEYLDFVAGIATCTLGHAHPAMVEAVNRQIQKLHHVSNLYYIREQGELAKWLVDRSCADRAFFCNSGAEANEGAIKLSRKYAHTVLNIDEPVILTANASFHGRTLATITATGQPKYQKNFNPLVPGFHYVPYNDFEAIAAAIAQLDGGEKRRVAAILLEPLQGEGGVRPGDRAYFQKVRQLCDEKGILLILDEVQVGMGRSGQLWGYEHLGIEPDIFTSAKGLGGGIPIGALLCKSSCDVFEPGDHASTFGGNPFACGVALAVCETLERENLVENARERGEQLRVGLQAIADRYPQLFVEVRGWGLIDGIEIAAESEVTSIEIVKAAIVEGLLLVPAGPKVVRFVPPAIVTEAEIDRALEMLDRAISTRVS
>NZ_CP051167.1|WP_168568851.1|2211051_2211252_-|hypothetical-protein
MLSGLQRKARANFVNDKKIPLGFQPNSREDWMEDFSDRFTIAGSPTDINHQEFYDYLKHRTDRDSK
>NZ_CP051167.1|WP_168568852.1|2213349_2214576_-|IS200/IS605-family-element-transposase-accessory-protein-TnpB
MFKAYKYRIYPTPEQQATLAKSFGCCRWYWNYALNLCQETYRATGKGLSRGDLQGLLPALKKEYPWLKEDVYSQCLQVVALNLSTAYRNFFEKRAKLPRFKSKQGRQSISYPQNVKFEGNYIKLPKVGLVRCRQHRSFEGKIKTVTLSKNPDGKYYVSVLVEGREEPPFPSTEGKAIGIDLGLTDFAITSEGSKYNNPKYFDKHARNLKRKQQKHARKRKGSNNHNKSRVKVAKIHAKISRCREDFLHKLSRKIVNENQVIVVESPLTPLNKGGTKGGIGMVRHHKLAKAISDVGWGMFCTMLKYKAESEGKVYLEVDRFFPSSKTCHVCLNQIKSLSLDARSWTCEHCQTHHDRDINAAINLKNEGLRILELGTRSTALGGDVRRGGRTSVLSSAVPSEEGSRYCNL
>NZ_CP051167.1|WP_168568853.1|2214742_2215642_-|hypothetical-protein
MAEPNQTIHITLPPLKITLKDGQQATLEWQPQAQNPPAPAPSPEDRSRYEIKAYPISSTEGWTIEPAPPRREWMDRIPHGFAYRCLPLVMANQMGWIVRCPTDFEAVWNGQMHYLNSIAIRFKEEGTPYEKLIASHFGSGILTFSLPWLFRTPPGIGLMVRGATNFFKFNAAPLDGAIETDWSPYSFTMNWKIVEKDIPVKFSKGDPICMLVPYPMDLLERFDAGFVSMESDPKLKQDYYQWHQSRNSFNQRRDRTPLEWQKNYYGGKGPDNTPAPNHRTSFKLSRFDRSKPSPQEGES
>NZ_CP051167.1|WP_168568854.1|2215727_2216804_+|potassium-channel-protein
MYSNFQKKYRRIRNELLAGGVGLAGVLLIGTLWYWLVEGWKLSDAAYMTAITLSTVGYMEVHPLGERGRLFTVSLIAMGLVSIGYIVNRFTEALIQGYFQDGLRLRQQQRLLDTLSNHYILCGFGRTGRQIAYEFSAENIPFVVIDTDPEQIQIAQDLGYITIQADATLDATLMKVGIDRALCLVTAMPSDAENLYTVISAKTLNPKIRSIARANSEEAVQKLQRGGADAVISPYITGGRRMAAAALRPQVMDFVDGIITGADRAFYLEEFRIEPGACPCEGQTLADTRLRSRSGALVLAIRRSDGNLIGGPTADTMVLPGDTLICMGTAQQLRRLNQILSPLKAKTPRLPRKFPPQP
>NZ_CP051167.1|WP_168568855.1|2216829_2217036_-|glycogen-debranching-protein
MTIWVNEQVDPSGMIYACIACSDEQQAQKCHQEFLENLSDEQKQTGWIARMRTVSSWDEVPVSALKLS
>NZ_CP051167.1|WP_168568856.1|2217492_2218863_-|tetratricopeptide-repeat-protein
MVKGIWQKWLGSGNSKPPRRQPEETTATPASPPPPLEAEDYELLFRQIREGMMTGWDRSRVVQFFEVLGSRGDDRLWAEWLRGYGDRLLAQNSSSRELAVVLTRLGQMQIGEFSKVAISIGSQLLERQMGVQTPPPPPVAPPPPPPATSATPSATEAGEDLQQESSEPPVSESGISEHEVSEHEVSEHEVSDSQVALSPDEYFQKGNEQVSQQDWEGAIASYRKAIEIKPDFGAAWINLGGVHFYAQQYPEALEAFDRATAFAADNPSLWFNHGFTLSMLNRPIEAIESYKKAIELKGDFIQAWQHRGIELSKLHRHEEAIACYEKAIQIKPDFAEGWTGRGNALMQLERYEEATTCYDRAIQSQSNYVEAWFNRGLVLMQQQKPQEAIASFEQVAQLQPQNDRAWINVGLIYLSLQNYDRAIAAFDTVLQLRPNDPDAIALREQALKQKERNPDA
>NZ_CP051167.1|WP_168568857.1|2218983_2219349_-|DUF1818-family-protein
MEKILKSGEGWRLGWNPQAEIYRGLVGSDDWAIELSESELDDFCRLLNQLATTMAQMAEELMEEERIACEAQSDLLWMEVEGYPEAYSLRFILNEGRRGEGFWPARVVPELIAAARVLKVF
>NZ_CP051167.1|WP_168568858.1|2219366_2220581_-|IS200/IS605-family-element-transposase-accessory-protein-TnpB
MLLGFKTQLKVNLTQRQKLARHAGVARHAYNWGHGLCLGILSHNAACRPDEKIKFPTAIDLHKWLNKLVKPENLWYYEVSKCVPQYALRHLAQAWQDCFKKKKSRPKFKKKGRQDSFTLDGTIKILSENKIQVPVIGILKTYERLSGNYQPKNVTISREADRWFISFKIDVNVTPTEKKTDVVGIDLGIKALATLSTGVSIEGIKAYKKYSNKLARLQRQVSRKSLGSANRKKSQLQVQKLHRRIANLRKDTLHKLTLQSCKNHAVNVIENLNGSGMMANHKLAKSIADMGFYEFRRQMEYKSQIYGSQLIIVDRFYPSSKICSNCGSIKDSLLLSERLFGCDHCHLKIDRDLNAAKNLEKIGRATAKLTPVDKSEPTPLVEAGSKIDSNVLFIKLSDLMGKFG
>NZ_CP051167.1|WP_168568859.1|2221465_2221882_+|SCP-2-sterol-transfer-family-protein
MSDLFSTQWMEQFKEAWNADEELTSSLAKINFNSIIGYGFKDSDRPTGFIEIVNGKAVNAGSYDGQTLNWDLRASRESWEKWLSQGLNMMGLSMAYMKRNIVFPVGDYGAMIKDPRMAGPFVKSFAVMGQVSTHSSVS

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Crispr_ID: NZ_CP051167_14

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_14

2935686-2935775

Orphan

N:A

Consensus_repeat	Method
TTGAATCCCCCCTAGCCCCCCTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051167_14

>merge|NZ_CP051167|14|2935686-2935775|CRISPRCasFinder
TTGAATCCCCCCTAGCCCCCCTTTGAAAGGGGGGGACCGGAAGGGGTTGTGGGTTGTGGGTTGTGGGTTGGATCCCCCCTAGCCCCCCTT

>NZ_CP051167|14|12|2935686-2935775|CRISPRCasFinder
TTGAATCCCCCCTAGCCCCCCTT	TGAAAGGGGGGGACCGGAAGGGGTTGTGGGTTGTGGGTTGTGGG
TTGGATCCCCCCTAGCCCCCCTT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168571858.1\|2939277_2940915_-\|acetolactate-synthase-large-subunit	unknown	unknown	gnl\|CDD\|236239
NZ_CP051167.1\|WP_168569355.1\|2918222_2922164_-\|DUF4347-domain-containing-protein	unknown	unknown	gnl\|CDD\|372982
NZ_CP051167.1\|WP_168569371.1\|2946198_2946402_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168569364.1\|2936841_2937726_-\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|187554
NZ_CP051167.1\|WP_168569361.1\|2930473_2932942_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225483
NZ_CP051167.1\|WP_168569358.1\|2925616_2926855_-\|VWA-domain-containing-protein	unknown	unknown	gnl\|CDD\|225187
NZ_CP051167.1\|WP_168569359.1\|2927000_2927822_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|225660
NZ_CP051167.1\|WP_168569368.1\|2942815_2944975_+\|RNA-binding-transcriptional-accessory-protein	unknown	unknown	gnl\|CDD\|225094
NZ_CP051167.1\|WP_168569372.1\|2947584_2950293_+\|bifunctional-acetaldehyde-CoA/alcohol-dehydrogenase	unknown	unknown	gnl\|CDD\|237515
NZ_CP051167.1\|WP_168569369.1\|2945047_2945392_-\|carbon-dioxide-concentrating-mechanism-protein-CcmK	unknown	unknown	gnl\|CDD\|132897
NZ_CP051167.1\|WP_168569363.1\|2935190_2935667_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168569370.1\|2945544_2945859_-\|carbon-dioxide-concentrating-mechanism-protein-CcmK	unknown	unknown	gnl\|CDD\|132897
NZ_CP051167.1\|WP_168569354.1\|2917189_2917921_-\|rhomboid-family-intramembrane-serine-protease	unknown	unknown	gnl\|CDD\|223777
NZ_CP051167.1\|WP_168569366.1\|2941015_2942380_-\|NAD-dependent-succinate-semialdehyde-dehydrogenase	unknown	unknown	gnl\|CDD\|143418
NZ_CP051167.1\|WP_168569360.1\|2928250_2929774_-\|T9SS-type-A-sorting-domain-containing-protein	unknown	unknown	gnl\|CDD\|367843
NZ_CP051167.1\|WP_168569357.1\|2924154_2925234_+\|PIN/TRAM-domain-containing-protein	unknown	unknown	gnl\|CDD\|227292
NZ_CP051167.1\|WP_168569365.1\|2938367_2939150_-\|exodeoxyribonuclease-III	unknown	unknown	gnl\|CDD\|197320
NZ_CP051167.1\|WP_168569362.1\|2933180_2935130_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|380205
NZ_CP051167.1\|WP_168569356.1\|2922753_2923986_-\|coproporphyrinogen-III-oxidase	unknown	unknown	gnl\|CDD\|236007
NZ_CP051167.1\|WP_168569367.1\|2942604_2942817_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168571858.1\|2939277_2940915_-\|acetolactate-synthase-large-subunit	gnl\|CDD\|236239	PRK08322, PRK08322, acetolactate synthase large subunit.	0
NZ_CP051167.1\|WP_168569355.1\|2918222_2922164_-\|DUF4347-domain-containing-protein	gnl\|CDD\|372982	pfam14252, DUF4347, Domain of unknown function (DUF4347). This domain family is found in bacteria and eukaryotes, and is approximately 160 amino acids in length. There are two completely conserved residues (C and G) that may be functionally important.	1.95707e-50
NZ_CP051167.1\|WP_168569364.1\|2936841_2937726_-\|SDR-family-oxidoreductase	gnl\|CDD\|187554	cd05243, SDR_a5, atypical (a) SDRs, subgroup 5. This subgroup contains atypical SDRs, some of which are identified as putative NAD(P)-dependent epimerases, one as a putative NAD-dependent epimerase/dehydratase. Atypical SDRs are distinct from classical SDRs. Members of this subgroup have a glycine-rich NAD(P)-binding motif that is very similar to the extended SDRs, GXXGXXG, and binds NADP. Generally, this subgroup has poor conservation of the active site tetrad; however, individual sequences do contain matches to the YXXXK active site motif, the upstream Ser, and there is a highly conserved Asp in place of the usual active site Asn throughout the subgroup. 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. Atypical SDRs include biliverdin IX beta reductase (BVR-B,aka flavin reductase), NMRa (a negative transcriptional regulator of various fungi), progesterone 5-beta-reductase like proteins, phenylcoumaran benzylic ether and pinoresinol-lariciresinol reductases, phenylpropene synthases, eugenol synthase, triphenylmethane reductase, isoflavone reductases, and others. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. In addition to the Rossmann fold core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	7.91906e-60
NZ_CP051167.1\|WP_168569361.1\|2930473_2932942_-\|hypothetical-protein	gnl\|CDD\|225483	COG2931, COG2931, RTX toxins and related Ca2+-binding proteins [Secondary metabolites biosynthesis, transport, and catabolism].	3.25874e-24
NZ_CP051167.1\|WP_168569358.1\|2925616_2926855_-\|VWA-domain-containing-protein	gnl\|CDD\|225187	COG2304, COG2304, Uncharacterized protein containing a von Willebrand factor type A (vWA) domain [General function prediction only].	8.34813e-60
NZ_CP051167.1\|WP_168569359.1\|2927000_2927822_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|225660	COG3118, COG3118, Thioredoxin domain-containing protein [Posttranslational modification, protein turnover, chaperones].	3.22258e-57
NZ_CP051167.1\|WP_168569368.1\|2942815_2944975_+\|RNA-binding-transcriptional-accessory-protein	gnl\|CDD\|225094	COG2183, Tex, Transcriptional accessory protein [Transcription].	0
NZ_CP051167.1\|WP_168569372.1\|2947584_2950293_+\|bifunctional-acetaldehyde-CoA/alcohol-dehydrogenase	gnl\|CDD\|237515	PRK13805, PRK13805, bifunctional acetaldehyde-CoA/alcohol dehydrogenase; Provisional.	0
NZ_CP051167.1\|WP_168569369.1\|2945047_2945392_-\|carbon-dioxide-concentrating-mechanism-protein-CcmK	gnl\|CDD\|132897	cd07057, BMC_CcmK, Carbon dioxide concentrating mechanism (CcmK); Bacterial Micro-Compartment (BMC) domain. CcmK1-4 and CcmL proteins found in Synechocystis sp. strain PCC 6803 make up the beta carboxysome shell. These CcmK proteins have been shown to form hexameric units, while the CcmL proteins have been shown to form pentameric units. Together these proteins further assemble into the flat facets of the polyhedral carboxysome shell. The structures suggest that the central pores and the gaps between hexamers limit the transport of metabolites into and out of the the carboxysome.	4.7928e-40
NZ_CP051167.1\|WP_168569370.1\|2945544_2945859_-\|carbon-dioxide-concentrating-mechanism-protein-CcmK	gnl\|CDD\|132897	cd07057, BMC_CcmK, Carbon dioxide concentrating mechanism (CcmK); Bacterial Micro-Compartment (BMC) domain. CcmK1-4 and CcmL proteins found in Synechocystis sp. strain PCC 6803 make up the beta carboxysome shell. These CcmK proteins have been shown to form hexameric units, while the CcmL proteins have been shown to form pentameric units. Together these proteins further assemble into the flat facets of the polyhedral carboxysome shell. The structures suggest that the central pores and the gaps between hexamers limit the transport of metabolites into and out of the the carboxysome.	4.57387e-36
NZ_CP051167.1\|WP_168569354.1\|2917189_2917921_-\|rhomboid-family-intramembrane-serine-protease	gnl\|CDD\|223777	COG0705, COG0705, Membrane associated serine protease [Amino acid transport and metabolism].	4.0283e-23
NZ_CP051167.1\|WP_168569366.1\|2941015_2942380_-\|NAD-dependent-succinate-semialdehyde-dehydrogenase	gnl\|CDD\|143418	cd07100, ALDH_SSADH1_GabD1, Mycobacterium tuberculosis succinate-semialdehyde dehydrogenase 1-like. Succinate-semialdehyde dehydrogenase 1 (SSADH1, GabD1, EC=1.2.1.16) catalyzes the NADP(+)-dependent oxidation of succinate semialdehyde (SSA) to succinate. SSADH activity in Mycobacterium tuberculosis (Mtb) is encoded by both gabD1 (Rv0234c) and gabD2 (Rv1731). The Mtb GabD1 SSADH1 reportedly is an enzyme of the gamma-aminobutyrate shunt, which forms a functional link between two TCA half-cycles by converting alpha-ketoglutarate to succinate.	0
NZ_CP051167.1\|WP_168569360.1\|2928250_2929774_-\|T9SS-type-A-sorting-domain-containing-protein	gnl\|CDD\|367843	pfam04151, PPC, Bacterial pre-peptidase C-terminal domain. This domain is normally found at the C-terminus of secreted bacterial peptidases. They are not present in the active peptidase. It is possible that they fulfill a similar role to the PKD (pfam00801) domain, which also are found in this context. Visual analysis suggests that PKD and PPC are distantly related (personal obs:Bateman A, Yeats C).	4.56551e-06
NZ_CP051167.1\|WP_168569357.1\|2924154_2925234_+\|PIN/TRAM-domain-containing-protein	gnl\|CDD\|227292	COG4956, COG4956, Integral membrane protein (PIN domain superfamily) [General function prediction only].	1.74916e-161
NZ_CP051167.1\|WP_168569365.1\|2938367_2939150_-\|exodeoxyribonuclease-III	gnl\|CDD\|197320	cd09086, ExoIII-like_AP-endo, Escherichia coli exonuclease III (ExoIII) and Neisseria meningitides NExo-like subfamily of the ExoIII family purinic/apyrimidinic (AP) endonucleases. This subfamily includes Escherichia coli ExoIII, Neisseria meningitides NExo,and related proteins. These are ExoIII family AP endonucleases and they belong to the large EEP (exonuclease/endonuclease/phosphatase) superfamily that contains functionally diverse enzymes that share a common catalytic mechanism of cleaving phosphodiester bonds. AP endonucleases participate in the DNA base excision repair (BER) pathway. AP sites are one of the most common lesions in cellular DNA. During BER, the damaged DNA is first recognized by DNA glycosylase. AP endonucleases then catalyze the hydrolytic cleavage of the phosphodiester bond 5' to the AP site, and this is followed by the coordinated actions of DNA polymerase, deoxyribose phosphatase, and DNA ligase. If left unrepaired, AP sites block DNA replication, and have both mutagenic and cytotoxic effects. AP endonucleases can carry out a variety of excision and incision reactions on DNA, including 3'-5' exonuclease, 3'-deoxyribose phosphodiesterase, 3'-phosphatase, and occasionally, nonspecific DNase activities. Different AP endonuclease enzymes catalyze the different reactions with different efficiencies. Many organisms have two AP endonucleases, usually one is the dominant AP endonuclease, the other has weak AP endonuclease activity. For example, Neisseria meningitides Nape and NExo, and exonuclease III (ExoIII) and endonuclease IV (EndoIV) in Escherichia coli. NExo and ExoIII are found in this subfamily. NExo is the non-dominant AP endonuclease. It exhibits strong 3'-5' exonuclease and 3'-deoxyribose phosphodiesterase activities. Escherichia coli ExoIII is an active AP endonuclease, and in addition, it exhibits double strand (ds)-specific 3'-5' exonuclease, exonucleolytic RNase H, 3'-phosphomonoesterase and 3'-phosphodiesterase activities, all catalyzed by a single active site. Class II AP endonucleases have been classified into two families, designated ExoIII and EndoIV, based on their homology to the Escherichia coli enzymes ExoIII and endonuclease IV (EndoIV). This subfamily belongs to the ExoIII family; the EndoIV family belongs to a different superfamily.	6.25753e-136
NZ_CP051167.1\|WP_168569362.1\|2933180_2935130_-\|hypothetical-protein	gnl\|CDD\|380205	NF033203, entero_EhxA, enterohemolysin EhxA. Members of this family are the RTX toxin called enterohemolysin or EhxA, because it is found in enterohemorrhagic Escherichia coli (EHEC) strains such as O157:H7.	1.13896e-09
NZ_CP051167.1\|WP_168569356.1\|2922753_2923986_-\|coproporphyrinogen-III-oxidase	gnl\|CDD\|236007	PRK07379, PRK07379, coproporphyrinogen III oxidase; Provisional.	0

>NZ_CP051167.1|WP_168569363.1|2935190_2935667_-|hypothetical-protein
MSNTNTTNQPYATLLDESLENVQSILTEFAKSQEFLAKIETAFGNDYDANGLAVIQQQWSNGDFASLPQIEILTGSQLSGANAAYAGENNTIYFSQDFLNKPRFQPRSRSPTTPKSIGATTAYGKAPTTKNQISVEGSVPCLPQPTAIGLQEDGIKGF
>NZ_CP051167.1|WP_168569362.1|2933180_2935130_-|hypothetical-protein
MVTYSTILPDSVYIDVEQNNQSYWKITINDGTSIDGVHNGWCIDWGTPPSDGIANVYSSYGSLSQNILSRINEENLDSINWILNKNWNSTQSPEGNGFQGEEVQNAIWSLIDEGNSIFPGTNDVDSNYIRQQALQNGNGFVPNADDNVVIILEPQSGGQVVIITPDIPENPALDIEKYVSTDGGKTWHDADNPSGPISLQDTFDPFFKFVVENTGDVHLSNITVSDTVYDLNGDAPGTDITINSLAVGETKEYIITAPWELGQHTNTASANASYIDITNTTRNVGDRDDANYFGAAPEIDLEKLVSVDGGETWHDADNPTGPALIEGTSDPVFKFVVTNTGNVDLTNVILSDSDYDLNGDAAGTDITIDLLGVGEVKEYTLTVPWEPAQHTNTGTVNTSYMDRNLSDSDDAHYWGKAIPKITEKRLCGVYVTKNSPDTVLNLFDIFEDADNDDSELTLTIENNTNPELFDAISIDAQTGLLTLDYSLQGKNVPGDAEITIRATDPDGLFVNYILPVSVLKNNDPFPDGKNCNEYFHGGNGQDVITGNGGNDTIFGGSSPDILIGGEGNDVLVGGKGNDAFIISPGDGVDIIEDFGDGKDQIGLDGGLSFDMLNIMQDGSDVLISANGELLMTLTDVDANQLKEKDFFLV
>NZ_CP051167.1|WP_168569361.1|2930473_2932942_-|hypothetical-protein
MTGDDGEDLLYGGAGNDSQDGGQGRDFLYGEADNDSMRGGSDDDTLYGHAGDDELYGDDGNDSLVGGAGADYQDGGAGDDTVSYYNSPEAIYMHLQPGRGLGGDAEGDVVRNVENIEGSEHSDTLIGDNGANVLSGLGGDDIIDGKAGSDSLLGGRGNDYLDGRQDNDFLLGNEGKDSIQGRSGDDTLDGGDGEDILDGSSGDDSILGGGGNDRISAGSHNDRVWGEAGNDLIDAGAGNDYIEGGTENDTLYGHSGDDTLLGGQQNDLLVAHTGNDLLHGGQGQDTLYADKDNNVLFGGRDDDYLYSGAGSDTFMLGVGFGVEYIYNFDHSKDNFGFIGDLRFDQLTFSPGENEFVSDTLIHYALSGELLAVLKGSPSFFQPDLPQIPPIPQINLPVSTPQTDRPNNGNANGNSNRPNPQTETNSLPNLPEIEIPIAIASLETEDLSETVSPTVTPTDPASTPTVEPTAEPTTPAEPTPTPVAEMPDPEPEANLPESEVVETPSPSPSQPAVEENPSTPSGEAIAETPTISQPESFPGMPSTQTPEPVTETPGETVILPLEDPTPVTPPPAERPSSPQEGSEPIAETPVEPPVEEPIAETPVEPPVEEPIAETPVEPPVEEPQPEPQPEPPVEEPQPEPQPEPDPPVNLTGGSGEDNFTGGSGDDSLSGNSGSDRLSGEAGNDLLIGDTGDDTIAGGDGDDTLTGGNNNDRLDGDAGRDFLDGGANNDTLTGGWGDDTLIGGQGKDWFVLSPDMGTDAIVDFTVNGGTRDTLVLTEGLTYEALAIAQMGENTAIRIAETDELLAVLNGVDASAIDASVFTIL
>NZ_CP051167.1|WP_168569360.1|2928250_2929774_-|T9SS-type-A-sorting-domain-containing-protein
MTGTRFTGNIQDPVIPFLFDIPGTAIDLQRPLIVTLYPNANLDVQLDLLGNGASIVGGPINTFTGGTPETTTNGPQPGVSYRAVVQTAAVPVPATATTGPFLLEINSENAANNVAATAPQLGNLTPQSINGFVGRSDINDWYNFRLPSAGTVSLRLSGLQDNADLELYEANGTTLILRSQNGGTSDEALENVNLAAGNYLVKVSANDTTANLPDGGRASTSYTLNLIPGGAVPGTTVTLSASGTPSEAGGGLGTFTLSRGSQTTGDLTVNLTFGGTATFGGATSDYGVIGANFAPTGTGTVTIPNGQSVVNFTVSPVDDALNDPNETIAVSLNPGTGYNVGTPNSASLTIADNDGGGTDPVTGLRVYRFYNTVTGTHFYTADENERNFVRDNLIGYNYEGPSFEAAPAGTPNTAPVFRFFNTQVGTHFYTIDPNEANFVRTNLMAFRDEGIAYNAYVQPAPGSDPLYRFFNTFTGAHFYTPSAVERDVVSNTLPFYRYEGVGYYVDV
>NZ_CP051167.1|WP_168569359.1|2927000_2927822_-|tetratricopeptide-repeat-protein
MGYSIEVYDHNFEEEVLAKSYETPIIVDFFATWCGPCQMLKPILENVAKEYDCIVAKVNVEENQYLAQAFKIEGIPDVKVIKEGKVVDSFVGVLPDDQLAEFLAKCNISSRIDERVAAIKTNISAGELEQAEQQWRSLLQDYPDNPKLAIAAAKFFIGIDRLEDAEAVISKLDEFDKNYEAQLKAIRSLIYFRKEAIHPSGDREIDRQFSKAAALTLEGQYEQALKLFIDIVETDRTYKNDGARKGAIAIFDLLGNDHPLTKEYRKKLMLALY
>NZ_CP051167.1|WP_168569358.1|2925616_2926855_-|VWA-domain-containing-protein
MKVGLYPALNDNNIDAGQASSQRQLSLSIAAIAEATDASIPLNLCLILDHSGSMHGSPLETVKEAAFRLIERLKPGDRLSIVAFDHRAKIIVPNQVIEDINSIKKKIDRLSADGGTAIDEGMKRGLEELKKGSKDTVSQAFILTDGENEHGSNDACLKFASQAAESNITLNTLGFGEHWNQDVLEKIADAAGGTLSFIERPDRAVEEFGRIFERIQSVALTNAYLIFDLTPKVRLAELKPIAQVAPDTIELPVQPKQGKYEVRLGDVMTDVQRVVLANLYIGQFPQGQQTIARVQVRYDDPATGQSGILSDPVAVDAQVLTAYRPSPNPEVQQHILALAKYRQTQIAEQKMQQGDRTGAATMLQTAAKTALQMGDKGAATVLQTSATQLQAGKELSEGDRKKTRIVSKTILQ
>NZ_CP051167.1|WP_168569357.1|2924154_2925234_+|PIN/TRAM-domain-containing-protein
MLDAIIILTFILAGAGIGFYGIDMLPASAIDRVTNVEGLRSVTAGFGALIGGAIGLSVQTTYRRAETQVRQMPIDVLITRSIGLVMGLLVANLMLAPVFLLPIPSEFAFIKPLAAILGSVMFAFLGVALADTHGRAFLRLINPHSLEAMLVAEGTLKPAATKVIDTSCIIDGRLESLLETGFLEGQLLIPQFVLQELQMVADASNDQKRVRGRRGLDILNRIEEHYPDRVVIHSADYDDLQTVDAKLVRLAQEINATLLTNDYNLSKVASVQKVPVLNVNDLTQAVRPVYLPGDSLDLKILKEGKEAAQGVGYLEDGTMVVVEEGGTHIGDEIRVVVTSALQTSAGRMIFARPHTSVVA
>NZ_CP051167.1|WP_168569356.1|2922753_2923986_-|coproporphyrinogen-III-oxidase
MKLHRVCPRGAYVHIPFCRRRCFYCDFPVSVIGDRKSGENSGTIAEYVEVLIEEIEATPRSPHPLETVFFGGGTPSLLTAAQIDRLLTVLDRQFGIASDAEISAEMDPGTFDRAKLSGYARSGVNRVSLGVQAFEDDLLKLCGRSHDAEDIFTAVENIRHVGIPNFSLDLISGLPHQSLEQWRRALDRAIAISPNHLSCYDLVVEPVTPFGRFYKPGDRPLPDDDLTAQMYRLAAEMLSRAGYEHYEVSNYAKKGFQCRHNRLYWENQPYYGFGMGATSYVGDRRCSRPRTRKEYYEWVARYKASGGAIDEPPTSTEDRLLETLMLGFRLSDGVNLLEIRESFGAESVAAIVETLQVYDKNNWIEGLDRSGAIGERRSPPARVRLTDPEGFLFSNTILASLFESLTVESR
>NZ_CP051167.1|WP_168569355.1|2918222_2922164_-|DUF4347-domain-containing-protein
MKVIEARHPQNEIALIDPNLPAWELLAAGIKKGIELIILDPVGDPLEQIAAALRDRPHTKAVHLISHGSPGTLHLGNISINGNHFDRYASLFNSFYQLSLNDPQFSVLLYGCNIAAGEIGRTFIEKLHHLTGANIAASSSPVGNRKRGGHWDLDAIAGKIGAQKAFSAPAMAAYPALLEVTFDSPSLYKVGNTPYFVALGDFNGDNHLDLAVANSGDDTISILLANDNGSFSPQTKFSVGDAPHSLAVEDFNGDGKADVVVANSSDTKVSVLLGDGNGSFNPEMTYEVGSKPPRSVAVGDFNSDGKVDLAVANSSWPMGSSIDDQVAILLGNGAGSFSLETTYQVGNGSDASLAVGDFNGDNNADLAVANYRDGKVAVLLGNGTGSFDSPIAYGVGDGASCVAVADLNDDGNSDLAVTTTSNNGVSVLLGDGTGNFNPQTIDEIGISSPTSVAIADFDGDGKLDLAVGCSWDYKIALLLQSANGVFGAANTYQAVKSPRSLAVGDFNGDGQPDLAAVNAVYDGNVSEVYSFYVGVFLNTTPVSPTPSTPVISIAPDTNADETESTEGTFDITLDRAAPTGGLTVNFNVAGTATKADDYNLSAGNNITEVTATSFTIAAGATNATLTVVPIDDNEVETDGETVEIQLEAGSNYTVNTTDNTAEIAIADNDSSEIEVKEPEIEVNDGTTEIEDGTTTILDWGSTPVGTPLSKTLTIANTGNADLNLSNLNLPEGFSIVGTLPSTIAPGTSGSLQIQLDAIAAGSFDGTLSFESNDADEDLFDFAIGAQVTDSGQSGDTTTTGGGTTTTGGDTTTTGGGTTTTGGDTTTTGGDTTTTGGGTTNTGGDTTTTGGGTTNTGGDTTTTGGGTTTTGGGTTNTGGDTTTTGGGTTTTGGDTTTTGGGTTNTGGGGWEAIAPQLPYCPSVPLEQRSLNTNSTPEAVQLPLPEFHLDCTCPPLPEIPAVCFGNPQVPSNNAGDDTLIGTESNNYLLGGRGNDFLQGLESSDTLLAGNGSPIPVGSLGDRDLIHANRGNDILQGCEGNDTLCGGKDNDIAHGGKDDDCIWGDLGSDTLMGDLGNDSLWGGTSNPDVRDVSGEDLLFGGAGDDFLNGDGGNDSLSGGEGNDTLRGAENDDLIQSNGGDDWLMGDEGNDRLCGSDGNDTIFGGLGSDRPIGSVGEKDVLGGGAGDDFLNGNEGEDRLCGGDGNDTLHGGKDNDVVGGGDGDDLLWGDLGDDTLIGGEGNDRFVLQAGAGTDAIADFVSGTDAIALAGGLTFAQLDLSETGTVTLIQFQDEVLATLIGVVNLSAADFTLIETSDSF
>NZ_CP051167.1|WP_168569354.1|2917189_2917921_-|rhomboid-family-intramembrane-serine-protease
MIPIDDNLPQRSPPIATTILIALNIAIFIIELHLDARGELTDFLNTWALVPARLTSMANDAIASQNPAAWVALLAMGGGSLLSAMFLHGSFSQILGNLLFLWVFGRKVEDILGHFTYFGFYLLCGILSGIGQAIAEPSLSAFLIGANGAIAAILGAYLLNFPKAKIDSLLPLIIVFIPVEVPAFFYSLWWFVQQIFYGIGELGGLYANINPSSTGYWLHGLGMAIGAGSIPFFVRFKPKTAIY
>NZ_CP051167.1|WP_168569364.1|2936841_2937726_-|SDR-family-oxidoreductase
MYLVTGATGGLGRRIVRVLRERDQKVRAFVRLTSRYGELENRGADIFIGDLTEERDIHKATQGVDYIISAHGSNEASGGAQALDYRANIELIDCAKACGVKHFVFISVLGCDRGYEDSPVFKAKREVEKYLQNSGLNYTILRPSGFASNLLPLAERVKETGIYLSVGDMKNRTSPVSTDDLAKIAVDSVTLEAATRQIFAVGGPEVLSRGELPRIFGRIFNREPFVINPPLTVFDGVRGILGFVNPDLQKSLGTLRVLLANEFFCTPEEIERLESTFDFKLETLESFVRRYLGA
>NZ_CP051167.1|WP_168569365.1|2938367_2939150_-|exodeoxyribonuclease-III
MKIATWNVNSIRTRAEQVTNWLQANPVDVLCLQETKVVDRDFPRSPFEDLGYHLYISGQKSYNGVALFSQTPMSDVAIGFSSLLGDAVAEFDLQKRAIAATLEDVRIVNLYVPNGSAVGSDKYEYKLQWLQVLHDYLKATGDRTDKICICGDFNIAPDDRDVYRDTKDTDIMASPAEREALQTQILDLGFIDIFRKFHEDGGHYSWWDYRRGGFANNRGWRIDHHYLTPALRDRARHCAIDIAPRRLERPSDHTPVVLEL
>NZ_CP051167.1|WP_168571858.1|2939277_2940915_-|acetolactate-synthase-large-subunit
MNTAELLVSCLENEGVRYVFGLPGEENLEVLRALSNSSIQFITTRHEQGAAFMADVYGRLTGKAGVCLSTLGPGATNLMTGVADANLDGAPLVAITGQVGTDRMHIESHQYLDLVAMFSPVTKWNAQIVRPSITPEIVRKAFKRSQTEKPGAVHIDVPENIAAMPAVGHPLTIDKQEKSYASYQGLNEAAAAISRATNPLILVGNGAIRAHAAAALTEFATRLQIPVANTFMGKGVIPYTHPLSLWTAGLQQRDYISCAFDHTDLVIAVGYDLIEYSPKKWNPEGKVPIIHIGAAQAEIDSSYIPIVEVVGDISDSLMEILHRCDRHGKPQPHACELRNDIRADYEQYADDSEYPIKPQKLIYDLRQVMAPEDILISDVGAHKMWIARHYHCERPNTCLISNGFAAMGIAIPGAIAAKLVYPDRKVIAATGDGGFMMNCQELETALRVGTAFVTVIFNDCGYGLIEWKQHNHYGESAFVKFGNPDFVKLAESMGLKGYRVESTADLVPTLKEALEQDVPAVIDCPVDYRENIKFTQKAGGLTCSI
>NZ_CP051167.1|WP_168569366.1|2941015_2942380_-|NAD-dependent-succinate-semialdehyde-dehydrogenase
MTIATINPATGETVKTFEAIADAEIEAKLAKAQQTFESYHRIPFAQKAQWLNAAADLLEGQAADWAKLMTLEMGKPIQGAISEAKKCAWVCRYYAEQAPHFLADVAVETDASRSFVRYQPLGAILAVMPWNFPFWQVFRFAAPALMAGNVGLLKHASNVPQCALAIADIFREAGFPDGAFQTLLVGSDKVAQIVADDRIKAATLTGSEFAGASLAATAGKAIKKTVLELGGSDPFIVLDSADVESAIATAVTARMLNNGQSCIAAKRFILAEAIADRFEQGLIEKFQSLKIGDPMDATTDVGPLATPDILAELDHQVQQSVQKGARALVGGAPLDRPGNFYPPTILSDIPIGTPAYEEEFFGPVALLFRVAGIDEAIKLANSTPFGLGASAWTADDAERDRLIEELQAGCVFINGLVKSDPRLPFGGIKRSGYGRELSVEGIREFVNIKTVWVK
>NZ_CP051167.1|WP_168569367.1|2942604_2942817_-|hypothetical-protein
MRSLMGAKLATIAYFIVLSVRRGEPIAPDKRQEKDPGVGKGSRNEHLEAIVANADFRFPTQHFMTKNLEI
>NZ_CP051167.1|WP_168569368.1|2942815_2944975_+|RNA-binding-transcriptional-accessory-protein
MLDLARIIADELAVKPTQVENALTLFAEGATIPFVARYRKERTGSLDETQLRHISERYDYLTELEDRKKVILETIAQAGKLTEELQAKIEACQQKNELEDLYLPYKPKRRTRATIARERGLEPLADWIKQLNLSKASAALTPEAARYLDPEKGVETVEDALKGAADILAEEIAERTESRAYLRDYFLKQGVFASRIKDDYPEGTTKYEMYRQFSVPVREIAPHNLLALFRGEKEGIINLTLDFDETEVLNYLESREIRTKVPEIRNFYRELIQDGFKRLMQNSLTSEVRSLKKEWADIESIETFEANLRELLLSAPAGMKPTLAIDPGFRTGCKVSVLDETGQFLEYQTIFPHTGDRQKVEAAKTISRLIAQYKIESIAIGNGTAGRETDRFIGDVLKTCDNPPIKVMVNESGASIYSASEVARDEFPDLDLTVRGAISIGRRLQDPLAELVKIDPKSIGVGQYQHDVDQKLLKKKLDDTVESCVNYVGVDLNTASKELLGFVSGLTPTIAKNIIAYRNENGAFKRRKQLLKVAKLGPKTFEQAAGFLRIRGGDNPLDNTAVHPESYAVVEAIAGDLGIPLTEIAKAGDRLKSVQLQKYTSDRVGLPTLRDILKELEKPGRDPRAEFKYATFKEGINEISDLRPGMELEGIVTNVTNFGAFVDIGVHQDGLVHISQLADRFVNDPKEIVKVGQVVKVRVLDVNEQLKRIGLSMRSRDRA
>NZ_CP051167.1|WP_168569369.1|2945047_2945392_-|carbon-dioxide-concentrating-mechanism-protein-CcmK
MPAQQAVGSIETKGFPGILAAADAMVKAGRVTLVGYIRVGSARFNINIRGDVSEVKTAMEAGIAAVESAYGATLESWVIIPRPHENVVAVLPIDYSPAVEEFRQAVDGLRLPSS
>NZ_CP051167.1|WP_168569370.1|2945544_2945859_-|carbon-dioxide-concentrating-mechanism-protein-CcmK
MPAAVGVIETLGFPAVLAAADAMVKGGRVTLVYFDKAERGNFVVAIRGPISEVKPAVEVGLEAAEKTFGGKVMSYYIVPNPPQNIVSVLPIEYTEAVEEWRSVW
>NZ_CP051167.1|WP_168569371.1|2946198_2946402_-|hypothetical-protein
MSDEIINVKPSTRNHKGFFVQHAAYKLIEIDKSGWALICLDDAVCHYVDPDSLQMQHRSTDNSQSSS
>NZ_CP051167.1|WP_168569372.1|2947584_2950293_+|bifunctional-acetaldehyde-CoA/alcohol-dehydrogenase
MTIPVTNTQELEDLIVRVKSAQAEYATYPQERVDEIFKKAALAANAARIPLAKMAASETGMGIIEDKVIKNHFASEIIYNKYKDEKTAGIVEEDPSFGYQKIAEPVGILAGIVPTTNPTSTAIFKALLALKTRNGIIFSPHPRAKKCTCEAAKVVRDAAVAAGAPADLIGWIDEPTVPLSQQLMQHPQINLILATGGPGMVKAAYSSGHPSLGVGAGNTPATIDETAHIKMAVSSILLSKTFDNGMICASEQSAVVVDAVYEQVKQEFSDRGAYFLNPEEREKVGNIIIVNGRLNAAIVGQSVEKLAELAGISVPPNTRVLIGEVEAIDESEPFAYEKLSPILAMYRAKDFYDAVDKAEALIKFGGRGHTSVLYTSPSNLEHRHYFEARMETGRVLINTPSSQGAIGDLYNFRLDPSLTLGCGTWGGNTVSENVGPQHLLNFKTVSERRENMLWFRIPPKVYFKYGALPIALRELAGKQRAFIITDKPLYELGITRSVQETLDRIGIKYDIFFDVEPDPSLATVNRGLAQMNVFNPDVIIAIGGGSPMDAAKVMWLMYEHPETDFEGLAMRFMDIRKRVYDLPPLGKKAMMVAIPTTSGTGSEVTPFAVVTDDRTGIKYPLADYALTPNMAIVDPELVLNMPRTLTAYSGIDALTHALEAYVSVCASEFTNGLALEAIRLLFKYLPSAYKNGSNDPKAREKVHYAATMAGMAFANAFLGVCHSLAHKLGSTFHVPHGLANALMISHVIRYNATDVPFKQTIFPQYKYPNAKWRYARIADHLHLGGETDEEKVENLVAAIENLKSELDIPLTIKEVLPEEEQGFYEEVEEMADRAFDDQCTGANPRYPLIQDLKELYVLAFRGCRVGSSMYHQASQEEVLKGDREFDSETVETGDRPLAESAS

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Crispr_ID: NZ_CP051167_15

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_15

3255890-3255980

TypeV

N:A

Consensus_repeat	Method
AAGGGGGATTTAGGGGGATCTCCCCA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051167_15

>merge|NZ_CP051167|15|3255890-3255980|CRISPRCasFinder
AAGGGGGATTTAGGGGGATCTCCCCAATCTAAACCTGTTGCCAAAGTCCGAAAGTCTCCCTTATGAAGGGGGATTTAGGGGGATCTCCCCA

>NZ_CP051167|15|13|3255890-3255980|CRISPRCasFinder
AAGGGGGATTTAGGGGGATCTCCCCA	ATCTAAACCTGTTGCCAAAGTCCGAAAGTCTCCCTTATG
AAGGGGGATTTAGGGGGATCTCCCCA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168569586.1\|3263222_3263924_-\|DUF4336-domain-containing-protein	unknown	unknown	gnl\|CDD\|372974
NZ_CP051167.1\|WP_168571877.1\|3256017_3257409_+\|asparagine--tRNA-ligase	unknown	unknown	gnl\|CDD\|235176
NZ_CP051167.1\|WP_168571876.1\|3254968_3255241_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168569580.1\|3257505_3257895_-\|type-II-toxin-antitoxin-system-VapC-family-toxin	unknown	unknown	gnl\|CDD\|350305
NZ_CP051167.1\|WP_168569571.1\|3245464_3247999_-\|hybrid-sensor-histidine-kinase/response-regulator	unknown	unknown	gnl\|CDD\|223716
NZ_CP051167.1\|WP_168569587.1\|3264006_3265971_-\|ATP-dependent-zinc-metalloprotease-FtsH	unknown	unknown	gnl\|CDD\|273520
NZ_CP051167.1\|WP_168569578.1\|3254490_3254943_+\|anti-sigma-regulatory-factor	unknown	unknown	gnl\|CDD\|225083
NZ_CP051167.1\|WP_168569581.1\|3258219_3258414_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168569583.1\|3260532_3260862_-\|type-II-toxin-antitoxin-system-PemK/MazF-family-toxin	unknown	unknown	gnl\|CDD\|367091
NZ_CP051167.1\|WP_168569572.1\|3248426_3248651_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_008055509.1\|3257884_3258118_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168569573.1\|3249215_3250259_+\|PleD-family-two-component-system-response-regulator	unknown	unknown	gnl\|CDD\|226229
NZ_CP051167.1\|WP_168569579.1\|3255388_3255781_+\|DUF2203-domain-containing-protein	unknown	unknown	gnl\|CDD\|235316
NZ_CP051167.1\|WP_168569576.1\|3252131_3252455_+\|(2Fe-2S)-ferredoxin-domain-containing-protein	unknown	unknown	gnl\|CDD\|239278
NZ_CP051167.1\|WP_168569577.1\|3252444_3253353_-\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|215315
NZ_CP051167.1\|WP_168569574.1\|3250311_3250968_-\|HEAT-repeat-domain-containing-protein	unknown	unknown	gnl\|CDD\|224331
NZ_CP051167.1\|WP_168569584.1\|3260849_3261110_-\|AbrB/MazE/SpoVT-family-DNA-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|198034
NZ_CP051167.1\|WP_168569582.1\|3258558_3260442_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227922
NZ_CP051167.1\|WP_168569575.1\|3251255_3251720_-\|CBS-domain-containing-protein	unknown	unknown	gnl\|CDD\|341362
NZ_CP051167.1\|WP_168569585.1\|3261220_3262891_-\|NACHT-domain-containing-protein	unknown	unknown	gnl\|CDD\|368582

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168569586.1\|3263222_3263924_-\|DUF4336-domain-containing-protein	gnl\|CDD\|372974	pfam14234, DUF4336, Domain of unknown function (DUF4336).	9.01331e-17
NZ_CP051167.1\|WP_168571877.1\|3256017_3257409_+\|asparagine--tRNA-ligase	gnl\|CDD\|235176	PRK03932, asnC, asparaginyl-tRNA synthetase; Validated.	0
NZ_CP051167.1\|WP_168569580.1\|3257505_3257895_-\|type-II-toxin-antitoxin-system-VapC-family-toxin	gnl\|CDD\|350305	cd18738, PIN_VapC4-5_FitB-like, uncharacterized subgroup of the PIN_VapC4-5_FitB-like subfamily of the PIN domain superfamily. The PIN_VapC4-5_FitB-like subfamily includes the Virulence associated protein C (VapC)-like PIN (PilT N terminus) domain of Mycobacterium tuberculosis VapC4 and VapC5 ribonuclease toxins of the VapBC toxin/antitoxin (TA) system, and Neisseria gonorrhoeae FitB toxin of the FitAB TA system. This subfamily belongs to the VapC-like family of the PIN domain nuclease superfamily. VapC is the PIN-domain ribonuclease toxin from prokaryotic VapBC toxin-antitoxin (TA) systems. VapB is a transcription factor-like protein antitoxin acting as an inhibitor. Other members of the VapC-like nuclease family include eukaryotic ribonucleases such as Smg6, ribosome assembly factor NOB1, exosome subunit Rrp44 endoribonuclease and rRNA-processing protein Fcf1. The structural properties of the PIN (PilT N terminus) domain indicate its active center, consisting of three highly conserved catalytic residues which coordinate metal ions, in some members, additional metal coordinating residues can be found. Some members of the superfamily lack several of these key catalytic residues. The PIN active site is geometrically similar in the active center of structure-specific 5' nucleases, PIN-domain ribonucleases of eukaryotic rRNA editing proteins, and bacterial toxins of toxin-antitoxin (TA) operons.	1.72938e-41
NZ_CP051167.1\|WP_168569571.1\|3245464_3247999_-\|hybrid-sensor-histidine-kinase/response-regulator	gnl\|CDD\|223716	COG0643, CheA, Chemotaxis protein histidine kinase and related kinases [Cell motility and secretion / Signal transduction mechanisms].	2.15e-151
NZ_CP051167.1\|WP_168569578.1\|3254490_3254943_+\|anti-sigma-regulatory-factor	gnl\|CDD\|225083	COG2172, RsbW, Anti-sigma regulatory factor (Ser/Thr protein kinase) [Signal transduction mechanisms].	3.27406e-26
NZ_CP051167.1\|WP_168569587.1\|3264006_3265971_-\|ATP-dependent-zinc-metalloprotease-FtsH	gnl\|CDD\|273520	TIGR01241, ATP-dependent_zinc_metalloprotease_FtsH, ATP-dependent metalloprotease FtsH. HflB(FtsH) is a pleiotropic protein required for correct cell division in bacteria. It has ATP-dependent zinc metalloprotease activity. It was formerly designated cell division protein FtsH. [Cellular processes, Cell division, Protein fate, Degradation of proteins, peptides, and glycopeptides].	0
NZ_CP051167.1\|WP_168569583.1\|3260532_3260862_-\|type-II-toxin-antitoxin-system-PemK/MazF-family-toxin	gnl\|CDD\|367091	pfam02452, PemK_toxin, PemK-like, MazF-like toxin of type II toxin-antitoxin system. PemK is a growth inhibitor in E. coli known to bind to the promoter region of the Pem operon, auto-regulating synthesis. This family represents the toxin molecule of a typical bacterial toxin-antitoxin system pairing. The family includes a number of different toxins, such as MazF, Kid, PemK, ChpA, ChpB and ChpAK.	3.25941e-35
NZ_CP051167.1\|WP_168569573.1\|3249215_3250259_+\|PleD-family-two-component-system-response-regulator	gnl\|CDD\|226229	COG3706, PleD, Response regulator containing a CheY-like receiver domain and a GGDEF domain [Signal transduction mechanisms].	3.20361e-107
NZ_CP051167.1\|WP_168569579.1\|3255388_3255781_+\|DUF2203-domain-containing-protein	gnl\|CDD\|235316	PRK04863, mukB, chromosome partition protein MukB.	0.00245251
NZ_CP051167.1\|WP_168569576.1\|3252131_3252455_+\|(2Fe-2S)-ferredoxin-domain-containing-protein	gnl\|CDD\|239278	cd02980, TRX_Fd_family, Thioredoxin (TRX)-like [2Fe-2S] Ferredoxin (Fd) family; composed of [2Fe-2S] Fds with a TRX fold (TRX-like Fds) and proteins containing domains similar to TRX-like Fd including formate dehydrogenases, NAD-reducing hydrogenases and the subunit E of NADH:ubiquinone oxidoreductase (NuoE). TRX-like Fds are soluble low-potential electron carriers containing a single [2Fe-2S] cluster. The exact role of TRX-like Fd is still unclear. It has been suggested that it may be involved in nitrogen fixation. Its homologous domains in large redox enzymes (such as Nuo and hydrogenases) function as electron carriers.	9.33533e-23
NZ_CP051167.1\|WP_168569577.1\|3252444_3253353_-\|alpha/beta-fold-hydrolase	gnl\|CDD\|215315	PLN02578, PLN02578, hydrolase.	2.70226e-81
NZ_CP051167.1\|WP_168569574.1\|3250311_3250968_-\|HEAT-repeat-domain-containing-protein	gnl\|CDD\|224331	COG1413, COG1413, FOG: HEAT repeat [Energy production and conversion].	2.11972e-19
NZ_CP051167.1\|WP_168569584.1\|3260849_3261110_-\|AbrB/MazE/SpoVT-family-DNA-binding-domain-containing-protein	gnl\|CDD\|198034	smart00966, SpoVT_AbrB, SpoVT / AbrB like domain. This domain is found in AbrB from Bacillus subtilis. The product of the abrB gene is an ambiactive repressor and activator of the transcription of genes expressed during the transition state between vegetative growth and the onset of stationary phase and sporulation. AbrB is thought to interact directly with the transcription initiation regions of genes under its control. AbrB contains a helix-turn-helix structure, but this domain ends before the helix-turn-helix begins. The product of the B. subtilis gene spoVT is another member of this family and is also a transcriptional regulator. DNA-binding activity in this AbrB homologue requires hexamerisation. Another family member has been isolated from the Sulfolobus solfataricus and has been identified as a homologue of bacterial repressor-like proteins. The Escherichia coli family member SohA or Prl1F appears to be bifunctional and is able to regulate its own expression as well as relieve the export block imposed by high-level synthesis of beta-galactosidase hybrid proteins.	2.98551e-07
NZ_CP051167.1\|WP_168569582.1\|3258558_3260442_-\|hypothetical-protein	gnl\|CDD\|227922	COG5635, COG5635, Predicted NTPase (NACHT family) [Signal transduction mechanisms].	5.49034e-16
NZ_CP051167.1\|WP_168569575.1\|3251255_3251720_-\|CBS-domain-containing-protein	gnl\|CDD\|341362	cd04586, CBS_pair_BON_assoc, Two tandem repeats of the cystathionine beta-synthase (CBS pair) domains associated with the BON (bacterial OsmY and nodulation domain) domain. This cd contains two tandem repeats of the cystathionine beta-synthase (CBS pair) domains associated with the BON (bacterial OsmY and nodulation domain) domain. BON is a putative phospholipid-binding domain found in a family of osmotic shock protection proteins. It is also found in some secretins and a group of potential haemolysins. Its likely function is attachment to phospholipid membranes. The CBS domain, named after human CBS, is a small domain originally identified in cystathionine beta-synthase and is subsequently found in a wide range of different proteins. CBS domains usually occur in tandem repeats. They associate to form a so-called Bateman domain or a CBS pair based on crystallographic studies in bacteria. The CBS pair was used as a basis for this cd hierarchy since the human CBS proteins can adopt the typical core structure and form an intramolecular CBS pair. The interface between the two CBS domains forms a cleft that is a potential ligand binding site. The CBS pair coexists with a variety of other functional domains and this has been used to help in its classification here. It has been proposed that the CBS domain may play a regulatory role, although its exact function is unknown. Mutations of conserved residues within this domain are associated with a variety of human hereditary diseases, including congenital myotonia, idiopathic generalized epilepsy, hypercalciuric nephrolithiasis, and classic Bartter syndrome (CLC chloride channel family members), Wolff-Parkinson-White syndrome (gamma 2 subunit of AMP-activated protein kinase), retinitis pigmentosa (IMP dehydrogenase-1), and homocystinuria (cystathionine beta-synthase).	2.51848e-62
NZ_CP051167.1\|WP_168569585.1\|3261220_3262891_-\|NACHT-domain-containing-protein	gnl\|CDD\|368582	pfam05729, NACHT, NACHT domain. This NTPase domain is found in apoptosis proteins as well as those involved in MHC transcription activation. This family is closely related to pfam00931.	7.23659e-12

>NZ_CP051167.1|WP_168569579.1|3255388_3255781_+|DUF2203-domain-containing-protein
MSSPPDPHRDRPESEEFDEFDRALAEVEQALDRFKQRYSDVRRDREQIEQLKQRREDVRREAKQTPKGDRSHRRELKEELEQIEAAIETLEIHLESQLFSWKTLKEPFWQAVRFGGLGIVVGWILKSCSG
>NZ_CP051167.1|WP_168571876.1|3254968_3255241_-|hypothetical-protein
MAQKTRDLSTLELAQALAERLALVERDWHKLKSNRAVRAREQVAAALVFLLKDNPEEALARLQQATGWLDRSLSAPPCPTHGDRASKRSS
>NZ_CP051167.1|WP_168569578.1|3254490_3254943_+|anti-sigma-regulatory-factor
MIAISPRPVGRTWNTISFASTLYLCPILDLLLADIPEQWHAEVRLGLQEALVNAAKHGNQLDPSKRVVVRFTTTGNEYWWAIADQGCGFACPCPCPTAQFDEDIPHEEGECGRGLYILNQIFDRVHWNDDGTELKLCKKFDRRSRLPLVW
>NZ_CP051167.1|WP_168569577.1|3252444_3253353_-|alpha/beta-fold-hydrolase
MTETFVRPTDTISGSYWIWRDRPIYWVGAGDPRSDRPPLLLIHGFGASTDHWRKNIAELQKDFQVWAIDLIGFGRSAKPDWVYSADLWRDQLHDFIQTQIGRPVVLAGNSLGGYASLCVAATRPESVAGVILLNSAGPFTATEPVAEPTPRRKLAKTALKWVFQQDWVSFAIFQWTRRRSVIRKTLLKVYLDQTAVTDRLVEEIYRPSCDRGAARVFASVFKTPQGEKVDALLDRMDCPLLTLWGQGDPWMNARDRSARFRQHYPQLSEHFLDAGHCPHDEIPDRVNALMREWILAQVAPKY
>NZ_CP051167.1|WP_168569576.1|3252131_3252455_+|(2Fe-2S)-ferredoxin-domain-containing-protein
MFMDKQPPKSPKYRAISICQHDSCRRNGSAAVLKAFETADLPEGVTVNPSGCLGQCSCGPTVKVNPDNVWYCRIKPEQIERIVTEHLQGEEPVEEWLNPRMHMRFSI
>NZ_CP051167.1|WP_168569575.1|3251255_3251720_-|CBS-domain-containing-protein
MPKTVADVMSRNPIAVNPETPLDEAIKILAERRISGLPVVDENGQLVGILSEGDLMWRESGVTPPPYIMLLDSVIYLENPARYQRELHKALGQTVGDVMSKKVLTVSPDKPLNEAARLMHEKGVHRLPVIDDRNEVVGILTRGDVVRVMASGNS
>NZ_CP051167.1|WP_168569574.1|3250311_3250968_-|HEAT-repeat-domain-containing-protein
MSITPESVKTLLQSEDLGDRIKGVNQLRQLDRATAFDLVQGAIGDRSPRIRYAAVSQMAHLGVENRELSLTVLRDRLLNDSEADVQSAAADALGALQLTEAFDELRHLYETTQEWLLKFSIVAALGELGDDRSFEILEDALKSDEELVKTAAISSLGELGDRRATPLLLPFATDPDWQIRHRLAQALGRLGGDEVRATLETLAEDEVDLVGQTARSYL
>NZ_CP051167.1|WP_168569573.1|3249215_3250259_+|PleD-family-two-component-system-response-regulator
MRSLADCHTNSKDTGELEPLNRRGVEIVENGLTLQSEDEERPLILIVDDDRAIRNMLVTVMHNQGYRVVTAVNGLEALQVYKERKPDMVLLDAIMPMMDGFDCCLELQRLQGSDRTPVLMITGLEDNDSVDRAFEVGAVDYVTKPIHWAVLRQRVRRLLEQARLYRELEAANQELRRLAFLDGLTRVANRRGFDQTLARHWHELAQSGAYLSLILCDVDCFKRYNDTYGHQAGDRCLQEIARTLRQAASYPTDFVARYGGEEFAVILPRTEAAAALYVAQKIRMGVRHLAIAHESSTVSPFVTLSLGVATMVPYPGTSETEAIAAADKALYQAKQAGRDRAILKILN
>NZ_CP051167.1|WP_168569572.1|3248426_3248651_+|hypothetical-protein
MTIAKASGDGDLAKVSGDDADGNFSQRSRGSGRRGRSPFDPNPGLGQLLGIRSGAIARKLRWNLTRFVKVLLKF
>NZ_CP051167.1|WP_168569571.1|3245464_3247999_-|hybrid-sensor-histidine-kinase/response-regulator
MIIEDEELRLTFKVASEEHLQKLDEGLLYLEKHPEDRGKLEELMREAHSLKGDAGMLGVKDIATLAHQWEHLLGSVKRDETTLTPEICDRLYHGLDAIRKLVNEAVTGENAQVNTFYVLAELMGAKDHPAEESSAATQAPAKKTPARPQDETSPEATPAIAETEETPEDAADRGDREATANEDRPEARDQGRPTPAPVAAERDGAERPQNDAQAPPNEPEEIAAQGEPAQTPTPKHTGGHLTRASEKHPAKTETATSEYRIDTIRVETRHLDALMTQAGELTVTKIRIAHRLAEVEDIVSLWEEWSRDAFLNRFALEEVGRGNHNGAFDRLNGFFHRVEERLERLGDLVTGVRNAVYEDNTRLDLIADELEEGIRTLRLLPLSNIFNLFGRMVRDLAKQQGKRVELVVEGGETRADKRILEEMKDPLMHMIRNAIDHGIETPREREAQGKPAVATIHLKGYQNATNILIEVSDDGRGLDVDKIKQTALQRGIVREEELATMNVQQVQNLIFAPGFSTRTFVTEVSGRGVGLDVVRANVERLKGTIQVESTPGAGCSVRIQLGTTLATAHVLLVSVEGIAYALPVEFIYMARLVPQREIFAIEGRDTILLDDRPISVVPLVELLELPARANAERSRPQEETLPCIVLQVGSERLGVLVDALVDEQDVVLKAQSKLLKRVRNVSGATILGTGEVCMVLNPQDLIESVRQKYPAIADPTPVAETTNQRSSILLVEDSIATRTQEKRILEAAGYEVVAAVDGMDALNKLDSRRFDAIVSDIQMPNLDGLGMTAKIRENQKYSEVPIILVTSLASDDDKRRGLQAGANAYITKTSFNQEVLLETLQRLI
>NZ_CP051167.1|WP_168571877.1|3256017_3257409_+|asparagine--tRNA-ligase
MMKRRIAEILRSSQPDETVTVRGWVRTKRELKEFAFIEVNDGSSMANLQVVLDRSLPDYEDLLKPLNTGASVEVTGTVVESPAKGQRIELKASAIALYGESDPETYPLQKKRHSFEFLRTIGHLRSRTNTLGAVFRVRNAASHAIHQFFQERGFLWMHTPIITASDCEGAGEMLAVTSLDLNNVPRSEDGAIDYTNDFFGKPAYLTVSGQLEAEVMAMAFSNVYTFGPTFRAENSNTSRHLAEFWMVEPEMAFCDLTEDMDLAEAFLKYVFKSVLENCPEDMEFFNKRIDDSVLATADNIINNEFERITYTEAIKYLEKASKKFEFPVEWGLDLQSEHERYLAEELFKKPAIVTDYPIEIKAFYMRLNDDNKTVAAMDILAPKIGEIVGGSQREERLDVLERRIREQGLNPENYWWYLDLRRYGTVPHAGFGLGFERLVQFMTGMTNIRDVIPFPRAPLSIDF
>NZ_CP051167.1|WP_168569580.1|3257505_3257895_-|type-II-toxin-antitoxin-system-VapC-family-toxin
MPNKYLLDTNILIYYFNNQPEVQDVFEEIDSRQAEGFYCPITWVELLCYPGLTEEQANEMREFLRLINCVFLTEAVLDTAAIIRRNYRLKLADGIIAACALVTGCILVTRNVDDFKRIDGLSLWNPFDK
>NZ_CP051167.1|WP_008055509.1|3257884_3258118_-|hypothetical-protein
MSNYQEILHQAQTLTSDEQKLLLKELATLVSQGEPSQEVQNTTESPRLNLNRWRGFLPKRVDALKFQLKIRQEWDAE
>NZ_CP051167.1|WP_168569581.1|3258219_3258414_-|hypothetical-protein
MNPTQYQLSLSFEQVLSLVKQLREADKLKLSEALSKDLLNSKLTHLLQAFKTDELSSFRDKSEF
>NZ_CP051167.1|WP_168569582.1|3258558_3260442_-|hypothetical-protein
MTNSTPTPADALIAALHEPGRENLLDLVRNPLRLTLLCMTWDGSSLQDIQAELYDRYLRKIYEWNRNLHELEKYAERCGTTTTKLKQDSHQQSDILKKLKQNLNRKLGELAKAALNLPQERFRLSQALVEKHLGEELDKTSLGYLALRLGWLNRVGKDGRGDGIFAFYHATFQEYFAALAVEDWDYFLPREHRDRPVDGKRYRIFEKQWKQVILLWLGRGDIEDEEKEAFIRALVEFKGGVRNFYGYQAYFLAAAGINEFKACSLADEIVRQIVKWGFGYFDIEKQEWQTFLDPIEKAARKAIPETIRQLAIIEFTAIIKNCSDEGIRRQAAASLGEIGQGNPDAIAELLQVIRTTEDEHTRRQVAESLGKIGQGNPDAIAELLQIIRTTEDKDTRRRAAASLGEILTTSQHYAGVVTALKDCLSDEVHQNNFDRFDECYKLIWNCAENLPYPEFYQAWHHPPTTPHPEVEDNTPATPFTQQCNLALLPQILNQAIQTHPVNCQIICIDGSRFSDPSNPALQIYTTLKKAGCRPSPDGKPRTIADLQAYCEDDLSEHQIALIFYEEPTDPPPQGFDIAVLNQLARFSHPPIAVVVPQPLPECRLPQFLESDPDLMATLLQWLQNLDR
>NZ_CP051167.1|WP_168569583.1|3260532_3260862_-|type-II-toxin-antitoxin-system-PemK/MazF-family-toxin
MGVVAQRFDVFLVNLDPTIGSEIQKTRPCVIISPDEMNRHIATVIIAPMTTKGKAYPTRIACQFQGKEGKIVLDQIRTIDKTRLVKKLGQISPDEQSGVLDTLAEMFSE
>NZ_CP051167.1|WP_168569584.1|3260849_3261110_-|AbrB/MazE/SpoVT-family-DNA-binding-domain-containing-protein
MSTVIRTRIVKIGNSQGVRIPKLLLEQSGIQTDVEIEVEGDRLTIRTARRLRNGWDQAFAAMAKEQDDVLLDRVNSTDWEQSEWEW
>NZ_CP051167.1|WP_168569585.1|3261220_3262891_-|NACHT-domain-containing-protein
MVNPFVKLTIAGGCVLGGVAFPPLLAGEGIVWGTALATALGSVAAGNAANVVDALLDGEGQISLENQDLTKAVGKAIAAVITLAAKQYPGKTRQYLEKIAAQAKDNWVKIAQQELTQHRYPELREAKLDQFLTPQEYQLTQQGNLTDTEWSDIFIRLNMKACKGGGFPIPAQVRQEVAELLHTTFPKALRETLKEDFAKDGKAWAGLTLQLLTGMQAQLSQLQASQGEVNVGEFSQILQQFQELETQLRGSVSQQQAFFTEISGRIDSGFAEVCQRLGVMETQITQLLQGLEKTLESLVAEIRSHFDVANPHLSLAEWRSIAELMLAERQALTANPAFKRVDVYVPLALVERRQTKERKPGLSLENREEGEREEGEREEEKITPIAEDEFFDRVLRQGKSPQSRGRRIAVIGEPGSGKTTRLQAIADWILAEHLGIPIWIELAQFTEPTLVDYLEKWLKSAGVEGAIASLQDHKEHLWLLMDGLDERVARIERPHVSQLLTGWMGLGRVIITCRVNVWEADRNAFSGFDVYRNLPFEADQMETFIRRFFAQSDREQ
>NZ_CP051167.1|WP_168569586.1|3263222_3263924_-|DUF4336-domain-containing-protein
MLKEVDIDIWVAEQPFRYLGLSVGIRMTVIRLANQELAIISAIQPSDTLVSELSKLGVVKHIIAPNLYHHLFAANFKSIYPQATFWAAPGLTIKKPELLIDQTIRGDRGELLPGLDFMVFNGLRVLGLNGVDLLNECVFFHSASRTLILTDTAFHFDKSFPLLTQFAARLLGGYKQLSPSVLERLATTEKEQVRQSVEGILLWDFERVIMAHGSIIERDGKEKFKKGYESFLR
>NZ_CP051167.1|WP_168569587.1|3264006_3265971_-|ATP-dependent-zinc-metalloprotease-FtsH
MAEDPNSNQSPKLSDIRRFGRSIIFLLVWLLLLNFLFFQSPQTTRVPYSEFLSQIEAGRVQKATVGGDRIEYTLREDSQGDRPPKTYETFPVASDGNLVRLLREHGVEFSAPRSHEGGTIAIILSWALPLLLLFAFWGWAMSRSRGGGGPAALTIGKSKARIYSEGSTGVCFDDVAGVDEAKVELEEIVDFLKHAAKYTRLGAKIPKGVLLVGPPGTGKTLLARAIAGEAGVPFFSISGSEFIELFVGIGASRVRDLFEQAKAQAPCLVFIDELDALGKSRMGAGPMLGTNDEREQTLNQLLAELDGFEPNTGVILLAATNRPEVLDPALLRPGRFDRQVVVDRPDKSGREAILKVHAKLVKLDDDVDLDKIAARTPGFAGADLANLVNEAALLAARKNRVAVMMADFNEAIERIITGLEKKSRILNELEKKTVAYHEVGHAIVAALMPGCGTVEKISVVPRGVGALGYTLQLPEEDRFLMVEDEIRGRIVTLLGGRSAEELIFGKVSTGASDDIQKATDLAERFVTLYGMSDRLGPIAFEKRQQQFLEGFANPRRAVSAKVSEEIDREVRAIVEGAHHMASAILELNRSVLEETATLLLEKEILEGETLRSHLAKISRPTELETWLNTGQEIPSPNDDGATVRGDRSVDIFLS

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Crispr_ID: NZ_CP051167_16

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_16

3601080-3603169

TypeIII

N:A

Consensus_repeat	Method
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	PILER-CR
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CRISPRCasFinder
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CRT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	PILER-CR
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CRT

27 spacers

cas2,cas1,csx18,csx1,cmr5gr11,cmr4gr7,cmr3gr5,cas10

The CRISPR arrays of NZ_CP051167_16

>merge|NZ_CP051167|16|3601080-3603169|PILER-CR,CRISPRCasFinder,CRT,PILER-CR,CRT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACTATCCCATCGGACTAGGTTTAATCTCATGCTTCTCGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACTCGGCTTTGGCCTATCATCAAAAGGTGCAGGATTGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACCCTCGATGTTTGCACCCTCTAAATTAACGCCTTCGAGATTGGGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACCTGACATCAACGTCAATTTTCACCTTATTCTGATCCTGAGGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACCTCCCCGATAGAACTCCTTGTTCGACCGCCGCGAGCCGTCGGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACAGCTGAGATCGGCACCCTCTAAGCATGCGTCACTCGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACGCCTTCCGTAAGTCTACACCACGTAAGAAGGCGCGGTCGAGGATCGCACCGCTCAGGTTGGCTCCCCGGAGAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACGTTAAGGTGTCTTTCAGAGAAAGCAGGACGCTCGCGGGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACCCCTGAGAGGTTTACACCTGAAAGATCTGAATTGCTGAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACCATACTACGAATTCGAAGATTTCCTCGCTCTGCCATTCCTGGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACATACCTTCACGGTCTGGCTCCTGAGGGCAGATGTTAAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACAGGCCACCTGGGCCGCTAAGTCCAGCATGTTTGAGGGAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACTTTAATGCTCGGAGGTCTATGCCCCCGTACAGCCGAGCCTCTGGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACGGATATGAAACTCTTGATGTTTTATCTCCGAAAGTATGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACTCTGGGAGGCAGGCGAACGCCCGAAGGATCTCCTCCTGAAGGAGGGAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACCTCATTCCAAACTTTCCTTTTTTGTTCGTGTAACTCAAATATAGAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACGAGGTCAGCGCCCCGGAGGTCAGCGCCCCGGAGATCGGGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACGAAAGAACCGCAATGTTTGAGAGAGAGATATCTAGAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACTCAGAATCTTTAAAGTAGCCCATTGGTTTTCCTGGTTCAGTGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACATAATATAATCGATCTTCGATTCCGCTATTTCTCGAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACGAAGAAGTGTTAGTAACTCCTGGGCTTTATCATTAGAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACTATTCGACCTAACGTGTGGAACTCATTTATTAGAATTAAAAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACATTTCTCGGAGGTATTCATCCTGGATTTGATTCAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACAATACTTTCGTATCCGCCAGTTCTGCTTCAGTGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACTTGATGAAGTCAGCAACATCTTCATACTCCAGAGGCTTCTCCCCTAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACAATAACTTATCAATATTCCATCCGTATCATTCTAAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACCTCCTCAAAGAGTTTCTCCCGGTTTTGTACTCCGGATTGGATGAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC

>NZ_CP051167|16|10|3601080-3601487|PILER-CR
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TATCCCATCGGACTAGGTTTAATCTCATGCTTCTC
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCGGCTTTGGCCTATCATCAAAAGGTGCAGGATT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CCTCGATGTTTGCACCCTCTAAATTAACGCCTTCGAGATTGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTGACATCAACGTCAATTTTCACCTTATTCTGATCCTGAG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCCCCGATAGAACTCCTTGTTCGACCGCCGCGAGCCGTCG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACAGCTGAGATCGGCACCCTCTAAGCATGCGTCACTCGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACGCCTTCCGTAAGTCTACACCACGTAAGAAGGCGCGGTCGAGGATCGCACCGCTCAGGTTGGCTCCCCGGAGAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GTTAAGGTGTCTTTCAGAGAAAGCAGGACGCTCGCGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CCCTGAGAGGTTTACACCTGAAAGATCTGAATTGCTGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CATACTACGAATTCGAAGATTTCCTCGCTCTGCCATTCCTG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATACCTTCACGGTCTGGCTCCTGAGGGCAGATGTTAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AGGCCACCTGGGCCGCTAAGTCCAGCATGTTTGAGGGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TTTAATGCTCGGAGGTCTATGCCCCCGTACAGCCGAGCCTCTG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GGATATGAAACTCTTGATGTTTTATCTCCGAAAGTAT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCTGGGAGGCAGGCGAACGCCCGAAGGATCTCCTCCTGAAGGAGGGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCATTCCAAACTTTCCTTTTTTGTTCGTGTAACTCAAATATAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAGGTCAGCGCCCCGGAGGTCAGCGCCCCGGAGATCGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAAAGAACCGCAATGTTTGAGAGAGAGATATCTAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCAGAATCTTTAAAGTAGCCCATTGGTTTTCCTGGTTCAGT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATAATATAATCGATCTTCGATTCCGCTATTTCTCGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAAGAAGTGTTAGTAACTCCTGGGCTTTATCATTAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TATTCGACCTAACGTGTGGAACTCATTTATTAGAATTAAAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATTTCTCGGAGGTATTCATCCTGGATTTGATTCA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AATACTTTCGTATCCGCCAGTTCTGCTTCAGT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TTGATGAAGTCAGCAACATCTTCATACTCCAGAGGCTTCTCCCCTA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AATAACTTATCAATATTCCATCCGTATCATTCTAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCCTCAAAGAGTTTCTCCCGGTTTTGTACTCCGGATTGGATGA


>NZ_CP051167|16|14|3601080-3603169|CRISPRCasFinder
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TATCCCATCGGACTAGGTTTAATCTCATGCTTCTC
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCGGCTTTGGCCTATCATCAAAAGGTGCAGGATT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CCTCGATGTTTGCACCCTCTAAATTAACGCCTTCGAGATTGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTGACATCAACGTCAATTTTCACCTTATTCTGATCCTGAG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCCCCGATAGAACTCCTTGTTCGACCGCCGCGAGCCGTCG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AGCTGAGATCGGCACCCTCTAAGCATGCGTCACTC
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GCCTTCCGTAAGTCTACACCACGTAAGAAGGCGCGGTCGAGGATCGCACCGCTCAGGTTGGCTCCCCGGAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GTTAAGGTGTCTTTCAGAGAAAGCAGGACGCTCGCGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CCCTGAGAGGTTTACACCTGAAAGATCTGAATTGCTGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CATACTACGAATTCGAAGATTTCCTCGCTCTGCCATTCCTG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATACCTTCACGGTCTGGCTCCTGAGGGCAGATGTTAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AGGCCACCTGGGCCGCTAAGTCCAGCATGTTTGAGGGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TTTAATGCTCGGAGGTCTATGCCCCCGTACAGCCGAGCCTCTG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GGATATGAAACTCTTGATGTTTTATCTCCGAAAGTAT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCTGGGAGGCAGGCGAACGCCCGAAGGATCTCCTCCTGAAGGAGGGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCATTCCAAACTTTCCTTTTTTGTTCGTGTAACTCAAATATAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAGGTCAGCGCCCCGGAGGTCAGCGCCCCGGAGATCGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAAAGAACCGCAATGTTTGAGAGAGAGATATCTAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCAGAATCTTTAAAGTAGCCCATTGGTTTTCCTGGTTCAGT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATAATATAATCGATCTTCGATTCCGCTATTTCTCGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAAGAAGTGTTAGTAACTCCTGGGCTTTATCATTAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TATTCGACCTAACGTGTGGAACTCATTTATTAGAATTAAAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATTTCTCGGAGGTATTCATCCTGGATTTGATTCA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AATACTTTCGTATCCGCCAGTTCTGCTTCAGT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TTGATGAAGTCAGCAACATCTTCATACTCCAGAGGCTTCTCCCCTA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AATAACTTATCAATATTCCATCCGTATCATTCTAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCCTCAAAGAGTTTCTCCCGGTTTTGTACTCCGGATTGGATGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC

>NZ_CP051167|16|5|3601080-3601558|CRT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TATCCCATCGGACTAGGTTTAATCTCATGCTTCTC
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCGGCTTTGGCCTATCATCAAAAGGTGCAGGATT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CCTCGATGTTTGCACCCTCTAAATTAACGCCTTCGAGATTGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTGACATCAACGTCAATTTTCACCTTATTCTGATCCTGAG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCCCCGATAGAACTCCTTGTTCGACCGCCGCGAGCCGTCG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AGCTGAGATCGGCACCCTCTAAGCATGCGTCACTC
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACGCCTTCCGTAAGTCTACACCACGTAAGAAGGCGCGGTCGAGGATCGCACCGCTCAGGTTGGCTCCCCGGAGAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GTTAAGGTGTCTTTCAGAGAAAGCAGGACGCTCGCGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CCCTGAGAGGTTTACACCTGAAAGATCTGAATTGCTGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CATACTACGAATTCGAAGATTTCCTCGCTCTGCCATTCCTG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATACCTTCACGGTCTGGCTCCTGAGGGCAGATGTTAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AGGCCACCTGGGCCGCTAAGTCCAGCATGTTTGAGGGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TTTAATGCTCGGAGGTCTATGCCCCCGTACAGCCGAGCCTCTG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GGATATGAAACTCTTGATGTTTTATCTCCGAAAGTAT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCTGGGAGGCAGGCGAACGCCCGAAGGATCTCCTCCTGAAGGAGGGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCATTCCAAACTTTCCTTTTTTGTTCGTGTAACTCAAATATAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAGGTCAGCGCCCCGGAGGTCAGCGCCCCGGAGATCGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAAAGAACCGCAATGTTTGAGAGAGAGATATCTAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCAGAATCTTTAAAGTAGCCCATTGGTTTTCCTGGTTCAGT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATAATATAATCGATCTTCGATTCCGCTATTTCTCGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAAGAAGTGTTAGTAACTCCTGGGCTTTATCATTAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TATTCGACCTAACGTGTGGAACTCATTTATTAGAATTAAAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATTTCTCGGAGGTATTCATCCTGGATTTGATTCA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AATACTTTCGTATCCGCCAGTTCTGCTTCAGT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TTGATGAAGTCAGCAACATCTTCATACTCCAGAGGCTTCTCCCCTA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AATAACTTATCAATATTCCATCCGTATCATTCTAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCCTCAAAGAGTTTCTCCCGGTTTTGTACTCCGGATTGGATGA


>NZ_CP051167|16|11|3601631-3603169|PILER-CR
	TATCCCATCGGACTAGGTTTAATCTCATGCTTCTC
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCGGCTTTGGCCTATCATCAAAAGGTGCAGGATT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CCTCGATGTTTGCACCCTCTAAATTAACGCCTTCGAGATTGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTGACATCAACGTCAATTTTCACCTTATTCTGATCCTGAG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCCCCGATAGAACTCCTTGTTCGACCGCCGCGAGCCGTCG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACAGCTGAGATCGGCACCCTCTAAGCATGCGTCACTCGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACGCCTTCCGTAAGTCTACACCACGTAAGAAGGCGCGGTCGAGGATCGCACCGCTCAGGTTGGCTCCCCGGAGAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GTTAAGGTGTCTTTCAGAGAAAGCAGGACGCTCGCGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CCCTGAGAGGTTTACACCTGAAAGATCTGAATTGCTGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CATACTACGAATTCGAAGATTTCCTCGCTCTGCCATTCCTG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATACCTTCACGGTCTGGCTCCTGAGGGCAGATGTTAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AGGCCACCTGGGCCGCTAAGTCCAGCATGTTTGAGGGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TTTAATGCTCGGAGGTCTATGCCCCCGTACAGCCGAGCCTCTG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GGATATGAAACTCTTGATGTTTTATCTCCGAAAGTAT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCTGGGAGGCAGGCGAACGCCCGAAGGATCTCCTCCTGAAGGAGGGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCATTCCAAACTTTCCTTTTTTGTTCGTGTAACTCAAATATAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAGGTCAGCGCCCCGGAGGTCAGCGCCCCGGAGATCGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAAAGAACCGCAATGTTTGAGAGAGAGATATCTAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCAGAATCTTTAAAGTAGCCCATTGGTTTTCCTGGTTCAGT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATAATATAATCGATCTTCGATTCCGCTATTTCTCGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAAGAAGTGTTAGTAACTCCTGGGCTTTATCATTAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TATTCGACCTAACGTGTGGAACTCATTTATTAGAATTAAAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATTTCTCGGAGGTATTCATCCTGGATTTGATTCA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AATACTTTCGTATCCGCCAGTTCTGCTTCAGT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TTGATGAAGTCAGCAACATCTTCATACTCCAGAGGCTTCTCCCCTA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AATAACTTATCAATATTCCATCCGTATCATTCTAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCCTCAAAGAGTTTCTCCCGGTTTTGTACTCCGGATTGGATGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC

>NZ_CP051167|16|6|3601631-3603169|CRT
	TATCCCATCGGACTAGGTTTAATCTCATGCTTCTC
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCGGCTTTGGCCTATCATCAAAAGGTGCAGGATT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CCTCGATGTTTGCACCCTCTAAATTAACGCCTTCGAGATTGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTGACATCAACGTCAATTTTCACCTTATTCTGATCCTGAG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCCCCGATAGAACTCCTTGTTCGACCGCCGCGAGCCGTCG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AGCTGAGATCGGCACCCTCTAAGCATGCGTCACTC
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAACGCCTTCCGTAAGTCTACACCACGTAAGAAGGCGCGGTCGAGGATCGCACCGCTCAGGTTGGCTCCCCGGAGAGTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GTTAAGGTGTCTTTCAGAGAAAGCAGGACGCTCGCGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CCCTGAGAGGTTTACACCTGAAAGATCTGAATTGCTGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CATACTACGAATTCGAAGATTTCCTCGCTCTGCCATTCCTG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATACCTTCACGGTCTGGCTCCTGAGGGCAGATGTTAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AGGCCACCTGGGCCGCTAAGTCCAGCATGTTTGAGGGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TTTAATGCTCGGAGGTCTATGCCCCCGTACAGCCGAGCCTCTG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GGATATGAAACTCTTGATGTTTTATCTCCGAAAGTAT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCTGGGAGGCAGGCGAACGCCCGAAGGATCTCCTCCTGAAGGAGGGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCATTCCAAACTTTCCTTTTTTGTTCGTGTAACTCAAATATAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAGGTCAGCGCCCCGGAGGTCAGCGCCCCGGAGATCGG
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAAAGAACCGCAATGTTTGAGAGAGAGATATCTAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TCAGAATCTTTAAAGTAGCCCATTGGTTTTCCTGGTTCAGT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATAATATAATCGATCTTCGATTCCGCTATTTCTCGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	GAAGAAGTGTTAGTAACTCCTGGGCTTTATCATTAGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TATTCGACCTAACGTGTGGAACTCATTTATTAGAATTAAAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	ATTTCTCGGAGGTATTCATCCTGGATTTGATTCA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AATACTTTCGTATCCGCCAGTTCTGCTTCAGT
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	TTGATGAAGTCAGCAACATCTTCATACTCCAGAGGCTTCTCCCCTA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	AATAACTTATCAATATTCCATCCGTATCATTCTAA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC	CTCCTCAAAGAGTTTCTCCCGGTTTTGTACTCCGGATTGGATGA
GTCCCCACTCGCTGGGGAAACTAATTGAATGGAAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168569825.1\|3600612_3600894_+\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP051167.1\|WP_168569829.1\|3614044_3618514_-\|SAM-dependent-DNA-methyltransferase	unknown	unknown	gnl\|CDD\|368199
NZ_CP051167.1\|WP_168569831.1\|3625885_3626359_-\|peptidase	unknown	unknown	gnl\|CDD\|367843
NZ_CP051167.1\|WP_168571816.1\|3618577_3619615_-\|IS630-family-transposase	unknown	unknown	gnl\|CDD\|315923
NZ_CP051167.1\|WP_168567320.1\|3591584_3591758_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168569820.1\|3595417_3595834_+\|hypothetical-protein	cmr5gr11	mkCas0065_cmr5gr11_CAS-III-B	unknown
NZ_CP051167.1\|WP_168569830.1\|3619650_3621927_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168569828.1\|3613256_3613853_-\|Uma2-family-endonuclease	unknown	unknown	gnl\|CDD\|368559
NZ_CP051167.1\|WP_168569821.1\|3595817_3597557_+\|RAMP-superfamily-protein	unknown	unknown	gnl\|CDD\|187792
NZ_CP051167.1\|WP_168569832.1\|3626572_3629230_+\|phospholipid-carrier-dependent-glycosyltransferase	unknown	unknown	gnl\|CDD\|224720
NZ_CP051167.1\|WP_168571895.1\|3593469_3594597_+\|CRISPR-associated-protein	cmr3gr5	cd09748_cmr3gr5_CAS-III-B	gnl\|CDD\|187879
NZ_CP051167.1\|WP_168569822.1\|3597561_3599103_+\|hypothetical-protein	csx1	mkCas0108_csx1_CAS-III	unknown
NZ_CP051167.1\|WP_168569824.1\|3599617_3600613_+\|CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|376633
NZ_CP051167.1\|WP_168569827.1\|3611914_3612919_-\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|223540
NZ_CP051167.1\|WP_168571896.1\|3603208_3607606_-\|DUF1998-domain-containing-protein	unknown	unknown	gnl\|CDD\|350184
NZ_CP051167.1\|WP_168569818.1\|3591769_3593491_+\|CRISPR-associated-protein-Cmr2	cas10	cd09679_cas10_CAS-III	gnl\|CDD\|187810
NZ_CP051167.1\|WP_168571897.1\|3621923_3625139_-\|DEAD/DEAH-box-helicase-family-protein	unknown	unknown	gnl\|CDD\|350769
NZ_CP051167.1\|WP_168569823.1\|3599342_3599621_+\|hypothetical-protein	csx18	cls000006_csx18_CAS-I:CAS-III	unknown
NZ_CP051167.1\|WP_168569826.1\|3609432_3611913_-\|S8-family-peptidase	unknown	unknown	gnl\|CDD\|173793
NZ_CP051167.1\|WP_168569819.1\|3594596_3595418_+\|type-III-B-CRISPR-module-RAMP-protein-Cmr4	cmr4gr7	cd09682_cmr4gr7_CAS-III-B	gnl\|CDD\|224255

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168569825.1\|3600612_3600894_+\|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.	2.30338e-33
NZ_CP051167.1\|WP_168569829.1\|3614044_3618514_-\|SAM-dependent-DNA-methyltransferase	gnl\|CDD\|368199	pfam04931, DNA_pol_phi, DNA polymerase phi. This family includes the fifth essential DNA polymerase in yeast EC:2.7.7.7. Pol5p is localized exclusively to the nucleolus and binds near or at the enhancer region of rRNA-encoding DNA repeating units.	9.1419e-06
NZ_CP051167.1\|WP_168569831.1\|3625885_3626359_-\|peptidase	gnl\|CDD\|367843	pfam04151, PPC, Bacterial pre-peptidase C-terminal domain. This domain is normally found at the C-terminus of secreted bacterial peptidases. They are not present in the active peptidase. It is possible that they fulfill a similar role to the PKD (pfam00801) domain, which also are found in this context. Visual analysis suggests that PKD and PPC are distantly related (personal obs:Bateman A, Yeats C).	8.05462e-07
NZ_CP051167.1\|WP_168571816.1\|3618577_3619615_-\|IS630-family-transposase	gnl\|CDD\|315923	pfam13358, DDE_3, DDE superfamily endonuclease. This family of proteins are related to pfam00665 and are probably endonucleases of the DDE superfamily. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction.	6.61756e-30
NZ_CP051167.1\|WP_168569826.1\|3609432_3611913_-\|S8-family-peptidase	gnl\|CDD\|173793	cd04847, Peptidases_S8_Subtilisin_like_2, Peptidase S8 family domain in Subtilisin-like proteins. This family is a member of the Peptidases S8 or Subtilases serine endo- and exo-peptidase clan. They have an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure and are not homologous to trypsin. The stability of subtilases may be enhanced by calcium, some members have been shown to bind up to 4 ions via binding sites with different affinity. Some members of this clan contain disulfide bonds. These enzymes can be intra- and extracellular, some function at extreme temperatures and pH values.	6.76512e-106
NZ_CP051167.1\|WP_168569828.1\|3613256_3613853_-\|Uma2-family-endonuclease	gnl\|CDD\|368559	pfam05685, Uma2, Putative restriction endonuclease. This family consists of hypothetical proteins that are greatly expanded in cyanobacteria. The proteins are found sporadically in other bacteria. A small number of member proteins also contain pfam02861 domains that are involved in protein interactions. Solutions of several structures for members of this family show that it is likely to be acting as an endonuclease.	1.05236e-44
NZ_CP051167.1\|WP_168569832.1\|3626572_3629230_+\|phospholipid-carrier-dependent-glycosyltransferase	gnl\|CDD\|224720	COG1807, ArnT, 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family [Cell envelope biogenesis, outer membrane].	1.45258e-26
NZ_CP051167.1\|WP_168571895.1\|3593469_3594597_+\|CRISPR-associated-protein	gnl\|CDD\|187879	cd09748, Cmr3_III-B, CRISPR/Cas system-associated RAMP superfamily protein Cmr3. 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.	2.8644e-07
NZ_CP051167.1\|WP_168569821.1\|3595817_3597557_+\|RAMP-superfamily-protein	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.	9.67352e-05
NZ_CP051167.1\|WP_168569824.1\|3599617_3600613_+\|CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|376633	pfam01867, Cas_Cas1, CRISPR associated protein Cas1. Clustered regularly interspaced short palindromic repeats (CRISPRs) are a family of DNA direct repeats found in many prokaryotic genomes. This family of proteins corresponds to Cas1, a CRISPR-associated protein. Cas1 may be involved in linking DNA segments to CRISPR.	9.96813e-104
NZ_CP051167.1\|WP_168569827.1\|3611914_3612919_-\|ATP-binding-protein	gnl\|CDD\|223540	COG0464, SpoVK, ATPases of the AAA+ class [Posttranslational modification, protein turnover, chaperones].	1.84829e-37
NZ_CP051167.1\|WP_168571896.1\|3603208_3607606_-\|DUF1998-domain-containing-protein	gnl\|CDD\|350184	cd18797, SF2_C_Hrq, C-terminal helicase domain of HrQ family helicases. Yeast Hrq1, similar to RecQ4, plays a role in DNA inter-strand crosslink (ICL) repair and in telomere maintenance. Hrq1 lacks the Sld2-like domain found in RecQ4. HrQ family helicases are DEAD-like helicases belonging to superfamily (SF)2, a diverse family of proteins involved in ATP-dependent RNA or DNA unwinding. Similar to SF1 helicases, SF2 helicases do not form toroidal structures like SF3-6 helicases. Their helicase core consists of two similar protein domains that resemble the fold of the recombination protein RecA. This model describes the C-terminal domain, also called HelicC.	1.42813e-17
NZ_CP051167.1\|WP_168569818.1\|3591769_3593491_+\|CRISPR-associated-protein-Cmr2	gnl\|CDD\|187810	cd09679, Cas10_III, CRISPR/Cas system-associated protein Cas10. 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; Multidomain protein with permuted HD nuclease domain, palm domain and Zn-ribbon; MTH326-like has inactivated polymerase catalytic domain; alr1562 and slr7011 - predicted only on the basis of size, presence of HD domain, and location with RAMPs in one operon; signature gene for type III; also known as Crm2 family.	1.5724e-20
NZ_CP051167.1\|WP_168571897.1\|3621923_3625139_-\|DEAD/DEAH-box-helicase-family-protein	gnl\|CDD\|350769	cd18011, DEXDc_RapA, DEXH-box helicase domain of RapA. In bacteria, RapA is an RNA polymerase (RNAP)-associated SWI2/SNF2 (switch/sucrose non-fermentable) protein that mediates RNAP recycling during transcription. The ATPase activity of RapA is stimulated by its interaction with RNAP and inhibited by its N-terminal domain. The conformational changes of RapA and its interaction with RNAP are essential for RNAP recycling. RapA is part of the DEAD-like helicase superfamily, a diverse family of proteins involved in ATP-dependent RNA or DNA unwinding. This domain contains the ATP-binding region.	1.38321e-58
NZ_CP051167.1\|WP_168569819.1\|3594596_3595418_+\|type-III-B-CRISPR-module-RAMP-protein-Cmr4	gnl\|CDD\|224255	COG1336, COG1336, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	1.01423e-22

>NZ_CP051167.1|WP_168569825.1|3600612_3600894_+|CRISPR-associated-endonuclease-Cas2
MLLYVIVYDLPDNKRRQKIHDLLEGYGQWVQYSTFECWLSSDKYAELQKRLRCQLNLDEDSIRFYPLSRHTVAQVETWGIGPPLWKMPGSTIV
>NZ_CP051167.1|WP_168569824.1|3599617_3600613_+|CRISPR-associated-endonuclease-Cas1
MRALYVSEQGCYLSLNDQLVRVKRQETLYAEVQLPLLQMILIFGKSQVTTQVIRACLWRNIPIVYLSRMGYCYGRILPIERGYRQLARYQDDLTLSDRLQVAREIVCTKLRNSRTVLMRQHRRQPSSSLDLVIQSLAVLVEKVRQADNIPRIMGLEGAGAAQYFSAFGDCLSSDEFIFGDRSRRPPGNPVNALLSFGYQVLWNHLLALIEVHGLDPYVACLHEGHRSHAALASDLLEEFRAPFIDAFVMYLINRKMMDVRDDFVYHNGGCYLNDVGRVKYLKAFVKRMEETITDEFGESQPKWDLLNQQVKAFKQFVYDPVKQPYVAYQIR
>NZ_CP051167.1|WP_168569823.1|3599342_3599621_+|hypothetical-protein
MYLTYRSALVRNISVAALNGLITLVILLIAPLGLAAVIGNTFLITLASFFTGTFADVVVRYLQPSHPPRSVAASLENDSALGQRHPNHLDHQ
>NZ_CP051167.1|WP_168569822.1|3597561_3599103_+|hypothetical-protein
MNLWIVTIGSSDIQLHSDATNKQQGRSQGEMSDEIWSYWYEDGIKNEHCYSVVFEPKRAFEDKDENYRIASRVLGNVYELSDEDTRTEIFDYLTFPLLSKFIKRLQSIDVPNKIALLLTDQSQIFSSEEQRQDIKSPYWDDTCKLEPILKRYFEKEFPNVELELMTLKLTPDEQPGLDDWNKVLELVQTELDAIKIEPDTVYVSHQAGTPAISSAVQFMSLARFRNNVQFLVSNEYTQQTRTIYRSTYLGAIQRQEAQALLEQHNYAGIRNILGLTADSLDEKAKSIKYLLDAAEQWNFAEFQKFKTIVQKRKLLEIKEFPWYQSGYESAYLAVVRLEQGSTVDALFHSFRAAEGSISKFLEKRYQSHIYRDPNHGPQVEISIRQELPNYFNSLSQPNKHKFERHQKIGLYGDPLYDLFKEARTEAKNHPDIKVVWEVAKSERNNLFHRLDGLQESELFGIWNTATEIDWKARLLACLNFIAKDELAEPFSSLEEASFMAQLHDRLREKIASF
>NZ_CP051167.1|WP_168569821.1|3595817_3597557_+|RAMP-superfamily-protein
MRQIPDAYKKVPMMFRSPIPGRSQLQYLDKDKKKAREAQDVEKWVSEWTDKSQLIPEENARDVETETFQAKSYQVSWRFVTNGGQDDGIVRPVIGASGIPFYPGSSMKGAFRQACEQAEQLGEIPEGTCNIYCGNETDITPGCLRFEGAYPTNDWREGLLDLVHPQQGWQVITPDTNKKPNGESAYAQISLDRPTLRFAISSAKPLSSQQWEQIWQIWEKAIASGLGSKVSGGYGQINQTSHRILYKAKLKGQGQAAKLIDETGEFRPNIFRAALRGHALRIFGGLTDESTAQNLVQHLFGGIQGNEPTVGLLGFQFQPSQLEIESFGSGQYAQPTYDVKGELIWFLTRPIADPNQERRLKNLVARLMQFAMIFGGFGKSWRRVDHRIFFEEYYEDTYKALIGCHWQWLDKSTKRRNVKVGRTEKIAEFIDRVRDTAREWIQCQNQPLNENQWASDWREAWHPRNVQVWGRVAEDMDDSVAVHWFHKSYQQRIQGIQSEGSIYKSSVTGKLGQISLIWHRMYPVILVKKNPEDPKQPIVKNTCRYLELITIFPDNSKECDRFLEFLHTHPENFQLLWGE
>NZ_CP051167.1|WP_168569820.1|3595417_3595834_+|hypothetical-protein
MGWKSYELDRAAQKLVLAARERDSKSLNQSYKMRMAVAYGLERFWGEHLRLAGKEKNKSIFWKETWDALQKIMKNAGVTIPNDRVNPDNTQQIQSMSEKLWKLSLEDQRVTLAVLTQLCDCIVWWTQRYKGGKNETDS
>NZ_CP051167.1|WP_168569819.1|3594596_3595418_+|type-III-B-CRISPR-module-RAMP-protein-Cmr4
MYNKAYGIIETLAPLHVGATAGEETGNLNLIFRDQFTQTGIIPGSSIRGRFRADMRSRHPGEEQRWYGHEAVEGRQDGGTTEALVKFEYASLVWFPVFCPGQPVVWVSCPLLLKRFKRLAGIDENVPAPYTAQRGLQGRQMQDRGKILFFNLGFLEIENEENLSQWIPHGTDLDANKLVVVHDNDIAMLHDMALYRQSRVKLLDDMKKVDTEKGAFFNTEALPEGSILVFPIALKEKGWKPFNEEQNSCELYFGGLESIGFGRCLVSLAGDYQ
>NZ_CP051167.1|WP_168571895.1|3593469_3594597_+|CRISPR-associated-protein
MSKFEYLITISPLGLMYGSAGAFLSPENLVGRSGSKFPPDAATVAGLFFNANRENQFIDHEQLQQNLVITGPFWANRDTPKQFYVPIPWYKILGDDDSDEWTLLEKKHNGQPIESGKSESSSDTQWCLGRHEWHRNNKDLQPEYSWQLIDNWEFSANQLHKNKGTTQAIAKAPWEFVSFLHPKIRADERHVVEQDGLFLENAVQLDRQYCLVYLSNYEIPDGWYRFGGEGHLVELETQLLPEKHKINLLLEQKIQHACALITPGVWGSNKLSYRYPKHASFPRKGMKLLTDKAIPYRYRLGHNKKDREQGEEKYKTGRLSRGRYAMPPGSVYVFKHPLNMNWWDFPDEWFPKEGFPLKHLGCSLCLPVKIQGVPQ
>NZ_CP051167.1|WP_168569818.1|3591769_3593491_+|CRISPR-associated-protein-Cmr2
MTEYTAITFAPVQGFIEKSRKLRDLYGASIVLSYLSSKLVESALSQGLEVISPGLPNLQKGMPNRILIKGKFERNDVEKVLLDEWKKVLVICREWIEENLGFPKDNYSWSQTEEQKGKQKGEWERWESYTWEIFWGHGNSVDRAMEDLETRKLKRGWTGINWMGESSSLTGTDAIAWHQLGRTLEKGEDPGRSLTPEEKDALELFYRRLSWLLDNPDYRVGKPHLSLQQLRDYEESKPEEIGKYIAPNERLSIPELVKRLVTYDAIADEIDMVKLKPTKNDPEFKDINRNAGYWTAWFMGDGDKVGDKLQILATRNPDNLEEGDRNLKTFTDLMRNWGKEFEKQSDSFTAGEMRVIYAGGDDFLGVLYSKESKNQENALKIKPSDAFEWLRKLPIYWEQLQKDIDDRLKLQFTFSVGFVWAGHQVPQRDILQHCREAEKRAKSLGRDRVTIRVVFNSGQYVQWTCPWDYLDILTKYRDRNQKTGAEANWNHIYSDWAQLKARHAIRLQTTENNPIVKDIALSLFDLYFDNAADRFRKQRKWVYLTGKIDDETIVKWLDDLIEIGWQLCRSSSI
>NZ_CP051167.1|WP_168567320.1|3591584_3591758_+|hypothetical-protein
MSKEPFWQAKIWGLLHDPALKALHDHTERGDEGFWHYLQIINDAIHAPSCQTSIKTI
>NZ_CP051167.1|WP_168571896.1|3603208_3607606_-|DUF1998-domain-containing-protein
MTGEALDVKNWQESLYNCLAANELVYQIADALKKPRLLPELVGDLQRRSDRPISEEEILAWLALGASSRKDNRPLLRPVIHGFIRGVGGAVVTFPSGQTRPQLWLSAEDAVGESGGDGLFRLPVTTCTTCGQHYFSHHVGDFKFFDKQPEGGQLTEHRVIWKPLSSERGGDRVILLDKLVTDDENIEDYTDDFLSSHSSEQDARTTGVGASRSLSSHSRERQYPNSTVPLYFCRHCGTLHDLFCDRCRGCGHPGGLIELLAVRQKSKYPGKLSSCVTCQALGRHGVGGYREPTRPVRAVTVSDVHVLAQNAIHYAERRRLLIFADNRQDAAFQSGWMRDRARRYRLRSLMYDRIQQSEVSIGDLTAYLDDLLDDDDELSRTLIPEVWDVERKEAAGQKHRQERKYFLRIAVLREIATGVKQRIGLEPWGRMKIHYLGLTPDLEFIQKWATFLRVSPEELIEGIASLLDVSRRGNILFDPEGRIFSRFWKEGDREIQRGYLPLLQGVPKGLKLQRDPADNANRVQQWLSAKGDTLARQAARNWGIHKDSIAEFYEELWELLTEQLKILVQVPLLSSRNQPLRGCNGVYQIDADKIRLTSHQGIYRCQICRRSHIRPTPKLTCMAWRCSGTLEYEEENADNYDLMVLDQQFTTLRAREHSAQVPAKEREILERLFKGDGEYVNTLVCTPTLEMGVDIGGLDAVLMRNVPPLPANYWQRAGRAGRRHRMAVNLTYARQASHDRAYFNDPMKLLNGAIAPPRFNLRNPLMVEKHVHATVLTVLHQLRRGEGNLTKGDREEIADILKTCFPTQVKPYLFDENGNVRQVPLSVDRLSHLIAKTEPILSEKVAQVFAQQWPTESVGVVTPAKLRDYILNTGDRLAEVIDRLWKRLQWSLNQMARLDAVRQRKGTLDPDEEALRQRCDRLVKKLKGIQSRRKRESEGYDDINTYSVLAAEGFLPGYGLEVGSVLGVAQVPRHLMGISDFELPRPSATALREYVPGNLIYANGHRFVPRFYHLEPQQQLTLFQVDVTNEAIAEVGVSRATPSSLSIASLRAVPICDVDLPHQSHISDEEDYRFQMAVSIVGSEQNRHSGGKAYQWGQKTALLRQGVHLRLVNVGAANWSGSVSLPYNNLGYPVCTVCGQTRSPLSSDGDRAKFAEDHAERCGQPVEPTGFFADIVVDVLTIQDCANRQEAYSIAEALRFGAANILEMELDDLQVLAIAYPGQEKVDAMLYDPMPGGSGLLDRICDRWIDVTSAALEVTVRCPAVCDTACIDCLFTYRNSYYHRHLNRHLATEKINEWGHELQFGHDIPPKLPNVEETSGEKPVNNPETILRDMLQRASFPTPAAQYAIDLGRPLGTTTPDFFYEDPTERFEGICIYLDGMSRHLHGDPDRQKRDRDIREQLRYEGYEVIEIPVGNLSDRGAMAKVFFRLGQILLGKAQAKTLRDNPESWFEVASSEASAAVNPG
>NZ_CP051167.1|WP_168569826.1|3609432_3611913_-|S8-family-peptidase
MVEKSRQFPHIYVPEKGKNEAYKRPPQGGGSKSPPERDRKEHAQFLEQAIDRAIQEARQQIKSRNSNVAVGVPGFYLEFQLKAEETAALKSLENRQKKIELVAVSQLPEQQDMVRATVFVPESAANYFLKKIEEYRDEDTKKNKPKNEALIARLEGVDIGTVQSLFTDEPALFPQDNREIWWEVWLRKGKKEGFEQVATILDVRINSHTLSFPEREIVLAMCNVEAMAQIIKNSDAVAELRLAKDTPSFFLEMRTREQDEWVEDLAARLLEPGKHAVSICLLDSGVVQRHPLLSPGLAQNDMHTVEPSWGVNDSPQWQGHGTAMAGLCLYSDSLMDFLATSEPVKLLHRLESVKILPNSGGNKPELYGAITEQGISLPEIHEPTRRRVLCMAVTSETLSNHRGTPSSWSAAIDRLCFNDGDFRRLMVISAGNIRQDIPVTNYLDINDTEPIENPGQAWNPLVVGAYTEKINIIDPNYQGWQTVAPGGDLSPRSRTSVTWETQWPIRPDVVFEGGNMAWDGQNPGESINDLCLLTTHYRPNLRMFDRISDTSSATALASYMAARIMSEHPNYRPETVRALIVHSAEWTPAMQKHFNGASSKTSRCNLVRRYGYGVPDLGRALQSAKNDLTLIIEDEIQPFYLEVNSVKLKEMKLHQLPWPQEKLEELGEANVELKITLSYFIEPNPGERGWAYRHRYASHGLRFQVKGSLESDRDFRWRINQAVREEEEDNPVSNHSDNEKWFLGPKARDVGSIHSDVWYGTAVELAQKDAIAVYPVGGWWKEKKYLDRYEAISSYSLIVSIRVPEVDVDIYTPVYNLVSTVVPIDI
>NZ_CP051167.1|WP_168569827.1|3611914_3612919_-|ATP-binding-protein
MPTARQVIALLKSHIEGEEQQFYSAALQIAAHEARQGHGKLALEIRDLINEAKNRQSAIEPKPGLIPLVQPKGELANLLSARYPDTKLTDMVLSSELELRLKRIITEQKQRNRLQEYNLSPRRKILLVGPPGSGKTMTAAALAGELQLPLFTAIYSSLIGKFMGETASRLQLIFDAMSATRGVYFFDEFDAIGTQRNSSNDVGEIRRVLNSFLLFIDSDTSESLILAATNHPNLLDEALFRRFDDVIEYDFPSNEMIQTLLENRLVLFEIAWNDWSEILSIARDLSLADLVRAADEAAKQAVLSNSDRIHKENLVYAILERKNITTQRSLTASS
>NZ_CP051167.1|WP_168569828.1|3613256_3613853_-|Uma2-family-endonuclease
MTQTLPETPPLVLQMSPAIEMTDQQFFTFCQQNRDYRIERTATGEITIISPTGSETGNRNFDLILQFGIWTKQNQTGIGFDSSTGFTLPNGAIRSSDVAWIKRERWNALTPEQKQTFAPICPDFVVELRSPSDNLKTLQDKLQEYIENGVSLGWLIDRKERKVYIYRPDRAVECLENPATVSAEDILPGFVLNLSTIW
>NZ_CP051167.1|WP_168569829.1|3614044_3618514_-|SAM-dependent-DNA-methyltransferase
MIMRCVVILFAEARNLLPRENPIYHESYGIQGLRELLTRQAGGRAGERLRNSFSAWPRLLSLFRLVYSGSAHPELIVPRYGGKLFVPGDSLSSDPIARALAIFENPANSPSDAMVYRMLELLTRSKVKVRQGRRSTWVEAPVDFSGLSSEYIGILYEGLLDFELRQVEADNPIVFLNLGDRPALPLQRLEEMDDKALKALVEKLKQKAKPSTSEDEEESDDDAEAEAEESEAEVDEEEEDSDTDADAEAEDGDRTLELRQRATNWAIRAVKVGSLVTKPKSKKREALAEYETAVETMAKRLILEVLLPGEWFLVRWGGTRKGSGTFYTRPQLAVPTVRRTLLPLAYNPPVDEALNPDGKASAAQWHPKTPQEILDVKVCDPACGSGSFLIAALGFLTDALYESLFYHGWLREDPITQQVRVEIAADAIPQWFAECVKDLPLTLEHIGRERDAPTSGEETSFSRHRLKRYVVERCIYGVDIDALAVELARLSLWVETMDKSLPFSFLDHKVKCGNSLVGCWFDRFQDYPVMAWERDAGDANHDKFVHHYREYVAKSGKKKGQAQQKGDKWTQGIKDTRNSRVKEELTALLKTLDPSKPIIADFETTFPLPKLPEAIHDEAVGIFLEWHDLPIDYDSEEKKENEYEQKFRQDKAIQQLKQAFDSWCAVWFWPGDELEIAPTPQHFFDPTPEMAQRVAELAQQYQFFHWELEFPDVFAGVNDGFTAIVGNPPWETLQPNSMEFFSNIDPLYRTYGKQEALAKQVEYFQSDPQIEKSWLLYCDNLKALSNWTKNVGFPFGDPEEDGGKFSLSRSSKETELLHDLWRQRRQQHIGYADKRHPFRYQGEGKPYTQKLFAELGHILLKDGGRLSLIVPSGLYSDKGAGDLRNLFLNCCQWTHLYAFQNERFVFKDIDHRNKMVMFTVVKGGSTDAIATRFRLGPGDSPTAQELETDILGDRNYLSVPASEIRKFSPNTGALLEIRSDRDLAILEKMYDNGVLLGDDSPEGWGIQYRQGDFNMTSDSKLFPPRPQWEAKGYRADEYGHWLKGNWQPYDGSPSILQRPEGLILSVDGTSAIHVDEVEDVALPLYQGIMIHQFDFSPKGWISGTGVRAIWEEITWEHKSIRPQYLITAKDAYGKPRMIRGTKPSVRRVARNTDYRTTICGLVPDMPCGDKASIFAPIQHIATLALPAYLNSYAFDSVVRSRVGGTQLDYHIAAEIPTACGSASENNQLLAIKVLQLNGAYTLFAEDWIKLRTKFANTHKIIARSWYQLWAITPHERLRLRCILDAVVAELYGLDIEDFTWILRDCDYPAAQVCDNAFARTLEPKGFWRVDKDKDPELRHTVLSQIAFHELKRLGLEPFLNLNDGEGWMLPDTVRLADYGLGHDPRAEEPQPVAARLGDRFLPWQLEGTIEDSWQECERHADNLRRLLGDTPQTFNQENNTTNDTPDTPRKTEKLPSDPDYVPPTDRFGNPLNVDLFGNIIEPKSKRKKQ
>NZ_CP051167.1|WP_168571816.1|3618577_3619615_-|IS630-family-transposase
MNIIDELDNFIENTTNTKEMKRALAAKMKLSGQPSKKIEEILNVSSSFVSQWKNKAIFEGVESLNLQYKGSKGYLKPEEKTQITSWIRQQEYLRLSDLKRYLQQEYNVIYSSNQSYYDLLKAAGMSWKKSQKKNPAKDEKLVKKKEEEIQKKLKDWEEDIKAGKLAVFMIDECHLLWGDVLGFVWGRKDIRVEIPIKNQKSRQSYYGALDYQTHEFILQEYPKADTDNTIQFIQYLREQRPGQKLAIFWDGARYHDSQQFRDFLKELNEGLEEDEWLITCTKFAPNAPEQNPVEDIWLQTKNFLRTFYFLCDSFKRVKELFKIFADGQVFDFPKLYSYGFLPQMT
>NZ_CP051167.1|WP_168569830.1|3619650_3621927_-|hypothetical-protein
MIATLSPTSTDENYEWWSALKHGGLLVAPSKLPEFFDRTLPPLPGYVEDRLRRDVTQYDRSDRDRFNRLCDTVLEDVLSLSKAQWIKAVDNRWTQRAITGEAIKPKRVWVHPQGMVLPLFEADASRLGIGKGRRQVSRVIEWLRKAEYKIALLTNGRQWRLIHAGVDYDAWCEWDIDLWFEEGKPGLQVMALRLLLGRDALEPPQPNAPCQLIQAIQASRQVQAELSGDLGERVRKAVELLIRETGVESGDSRSASVPARLEPHIRGYNNISGQDARTPGNNDRTAGSASVPARSDNLNSVPARLEPDNISGDHQISGQDARTPGNNDRTAGSASVPARSDNLNSVPPRLEPDNISGDHQISGQDARTPGNNDETARSASVPARSDNLNSVPPRLDPDNISGDHQISGQDARTPGNNDETAGSASVPARSDNLNSVPPRLEPDNISGDHQISGQDARTPGNNDRTARSASVPARSDNLNSVPPRLDPDNISGDHQISGQDARTPGNNDETAGSASVPARSDNLNSVPPRLEPDNISGDHQISGQDARTPGNNDETAGSASVPARSDNLNSVPPRLEPDNISGDHQISGQDARTPGNNDRTARSASVPARLDNLNSVPARLEPHIRGHNNISGQDARTPGNNDRTAGSASVPARSDNLNSVPPRLEPDNISGDHQISGQDARTPGNNDETAGSASVPARSDNLNSVPPRLEPHIRGHNNISGQDARTPGNNDETARSASVPARMNNIAVLNDSWKLFLL
>NZ_CP051167.1|WP_168571897.1|3621923_3625139_-|DEAD/DEAH-box-helicase-family-protein
MLATVRNRRALVVSVEPFDGGIAGRLHLVGLEYTDMDGNREDKVIWERELNASLLEPTALPRVDAEPPMQGEEFDALQRAARWTALSPFLNSDRREPLEPLPFSAPLFGAVQVEDFQLVPLYKALRMPRISLLLADDVGLGKTVEAGLILTELLLRRRIRRVLILCPAALRKQWQQEMKAKFSLSFDVVDRAETHAIQKRLGLDANPWRTYPRIITSYHYLRQPDVLEQFRTTLRQPEGSANLPWDLLIVDEAHNLMPANFGDDSDLSKMLRFISPWFEHKLFLTATPHNGHTRCFSGLLEQLDPVRFMQTGEMDAAQQQRIEEVVIRRLKREINQLDENRGEMPRFCQRIPQPVPLFFGKAERQLGRAFSEFRTAVKAAIADSKKTDRLAGSFAVEVLNKRLLSCPYTFAQSWVRFQEGIAGVDEAEVSQVQAAKRAIAEDIDDDLETEGRIQYAAKTTGAWLKPLVPDLTAEIAALDSALQALGLVEGGQLADPVEDERFSRLLTAIKQYLRNGKEWIPEERLVVFTEYKTTLDYLDRRLKAEFPGEPEAIRVLYGGMSDRDRDGIKQAFNDPADPIRILVATDAASEGLNLQETAHLILHYDIPWNPARLDQRNGRLDRHGQARDVIVFHFTSDDDADLKFLAHVVQKVNTIREELGSMGEVFDAAFQRRFIDFEDSDRVVRGLDEAVEKQRGRATVPRSPHTDTGSDCAIALQEFEKELDLTPETLKSTLEIAMGLGVGLPRFEGPDTEGKLRLQVPIPPKWEPLVDDYLRLETNGDRGALPAIVFDPSHFIQYRNNRPVFRAAKDTALLHLGHPIFYHALALFARARFPGGIDNLPVSRWTVRYGEVPDNADALLLLTVEELAVNELRESFHHWVRTLRFPIVGEELGEQLSHVAPVVKDYRDRLPDEAAIETAQELWDAIAFDLREKVQQIAQQLTEQLHPILKTQKAAGLEEAKKRFESRIKEVERAMKETTLQKLEKERERLLAEMERNPYLFPDLQREQAEKLQNLEDELKRRRHQYQGLLDFLKKEQNRTVKHLIPKRHTLRGTAQVFPVTVEIRLPEVSR
>NZ_CP051167.1|WP_168569831.1|3625885_3626359_-|peptidase
MTNRFAFAQRLPCRIDWHRIVLLPITVVAIAGSASGVRAENMYNPIRLPGSNEISDTLSEQDIPTGQGGFARDYIVTLQEGDQVAIDLLSDSFDTIVALIAPDGTTIAENDDGPDGSTNSLLFSRITQGGDYIVRVRAFGEGGTGNFTLKVTRLRPI
>NZ_CP051167.1|WP_168569832.1|3626572_3629230_+|phospholipid-carrier-dependent-glycosyltransferase
MIELNSRWHRTIALGAIWLLQSGCDRLWFALDRSVPDWDRADYLTGALNYADALEHPHWFSGEWWTNLWLLSSKIPPGTYLATAVIHQIFGTGSDRATLVNLLFSAILLASTYGLGRILFNPKIGLWAAALCTLFPAFYRSRLDFLLDYPLTATVTLAFFCLTLWRSRTHSPRLHTRPPSRFKLPPTLEPWLWAAAFGMASGLALMVKQTALLFLSVPLLWAAIASFKGRKWSQCGQLSLSVAIAALVIYPWYRTNWLLILTGSKRATVDAAIAEGDPSLTSLDAWTYYAEQLPNHVSWLLAIVAIVGFLLYYRRRQKDLSPSPVPHPWRWLAVYLLGAYFFASVNINKDFRYVLPYLPAVAIALAYGLSCWRGKWARSVRWGTLGIAVLLALNHLFPWGFTLPGSALLGDRADRRPYTGPPWPHPEAIAEIINTSPYLQTTVGVLPSTPEINQHNVNYYGALADFQVYGRQVGTRLSQVDRDMRSLDWFVTKTGDPGSVPEDAYGAISAAIAQNPDLILQREWTLPIPETAGQQDPSTLQLYRRQPPGVAVEPIADRSPSLPVRLDRAIVPPASPPGVPVPVTYYWSGPWEPLQRGLAIVTWENDNGDRWLHDRAIAGGRLYSQIDTSVPVRVVDRTAMLPPADLPPGVYRLQVTYLNRETGEIYPIAAPEVSLTIDENATPTPAPELDWVTQLRSLSQAMPRGPDALGPVFEEVARINQYDPVQDYLAQAARSLEYRLQSQPERLDFIYNLTLARVLQRDPQGAIAALKRATVLDAQNPYAHAYLAFVYLYDWQPRSAREPLDRAFALAPDLEVLQLLSAVSYLMQGNLFGVWSQVEGFLPDRLKTILAIAFAAFVALSISALLSIFVLHRRRFGRKRGSKSM

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Crispr_ID: NZ_CP051167_17

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_17

4026455-4029482

Unclear

N:A

Consensus_repeat	Method
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CRISPRCasFinder
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CRT
CTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	PILER-CR
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	PILER-CR

41 spacers

csb2gr5,cas7,cas8u1,cas3

The CRISPR arrays of NZ_CP051167_17

>merge|NZ_CP051167|17|4026455-4029482|CRISPRCasFinder,CRT,PILER-CR,PILER-CR
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACGGTTCATTAATTCGGGGTCGAGTTCTATTAATAATTCCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACAATATATAAAACATAAAAAAGAAAGGGAATATATTGGCCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCGATCGCGCGCCGACGGCGACAAAGAATAGGGCCCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACACCCTTCAACCCTCCGGTAGCTCTGACGGTAGGGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACGGGAATCCAATCCCGGCAGGCTCGGGGAGAGGCCTACGAGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACTCATCTGGATACTCCGCACTGATTGGATCCCAAATGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACGGATCCCGACGAGTATTTTCTCTCATTCCAGGGAGGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACAGATTCCGACCTGTCTGGCACCAACCTCTCTGGGCGCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCTACCCATTCTCCAATACTAGGGGTTACCGAGTAGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCCTGTGCCTTACTCGTACTACGTCCACTATGGCTAGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACTGTCGAAAATCAACCTCTCTGGTCGCGACCTGAGCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCTTAGGAATGGGCGCCATTTTTCGAGCTTGGCATTGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCCAAAAAAATCCGAATCGTCGGTCACCGAGTAAGGGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACGGAACGCGGTGTCCGGGACGGGAATCGCCGCACTGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACAGTCATCCTCGGAGCCACCTGTCTGGGCATCCTCGGGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACATAATCGAAGCATACGAACAAAAAAAAAGGAAGTAGAGGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCTATCTATCCCCTCCACCTGGATGATCAAAATTGGACCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCTGGGATCTGCGATCTCCAGTCCCAAAAAGTTCGCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACGCTCCCTACGCCCATTGATAATTAGATAGCACCCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCCAGGGTGCGATCTATTCTCCCATGAGAATTTCGGCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACGGTGATGTTTGTCAAGCTTTCGTTCAAAAGTGAGAGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACAGTCGCACTTTCTGCCCTAGCATTTCGGCTTTAGGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACGTTCTGGCGTTTTCGTAAGATTTTAAAAAATTATCGGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACTCGCTCCCGTTCCCGACATTAGCCAACTGCGGAGCTCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACAGGGCTTGAGATGCCGCATTAGTAGTAGCAGCATAGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACTTGATTAATTGATTAGACATAGTTGATTGTTCCTTTTGATGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACGCACGAGGAGATTGACCCGGTAGGGGTGGAATCCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACGCAATAGGGGAGGATGTCAACGGCGGGAGAGTCCGAGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACATGGTTCCTGATTGGTCGAGTCTTTCGCAATTCCCGTGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACTCATTTGCAACGTATCTTTAAAAGGTAAACACGAAGCCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCACTCTCCGGAAGCGCTCGACGGATCCCCCGAACCGTGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCAGTAGAAGACTAAGCTGCTCGTATTTTGGGATGTGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCCATCGGCGGCAATGTTGCTCCGGGGTCATGGGGAGGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACAGGACTCTCTCAGCCTCGGCCTTTGATGCAGCATAGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACATCATTTTTCTCCTGGTTGGGCGATCGTTTTTCGCGATGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACATCGGATCTATCCACTCGATGGCCGCCGCTTGCCTCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACTGAAGGCGTCTGTAGTGGTTTAAGTATAATGGGAAAAGAGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACTGTTGTATACTTTGGAACTTTTCCCAATGGTGGCTCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACTCGTCCAATCGACCTGAAACTCAACTCCTACCTAGGGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACGCTTGGGACTTTCCGGCCTTCGGACGCGGTCTGGGTAGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCTGGGGCAGCTTTTCGAGTCGAAGCTCGGAAAGTCAGGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC

>NZ_CP051167|17|15|4026455-4029482|CRISPRCasFinder
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGTTCATTAATTCGGGGTCGAGTTCTATTAATAATT
CCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AATATATAAAACATAAAAAAGAAAGGGAATATATTGG
CCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CGATCGCGCGCCGACGGCGACAAAGAATAGGGC
CCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ACCCTTCAACCCTCCGGTAGCTCTGACGGTAGG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGGAATCCAATCCCGGCAGGCTCGGGGAGAGGCCTACGA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCATCTGGATACTCCGCACTGATTGGATCCCAAAT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGATCCCGACGAGTATTTTCTCTCATTCCAGGGAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGATTCCGACCTGTCTGGCACCAACCTCTCTGGGCGC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTACCCATTCTCCAATACTAGGGGTTACCGAGTA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CCTGTGCCTTACTCGTACTACGTCCACTATGGCTA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TGTCGAAAATCAACCTCTCTGGTCGCGACCTGAGC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTTAGGAATGGGCGCCATTTTTCGAGCTTGGCATT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CCAAAAAAATCCGAATCGTCGGTCACCGAGTAAGG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGAACGCGGTGTCCGGGACGGGAATCGCCGCACT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGTCATCCTCGGAGCCACCTGTCTGGGCATCCTCGG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATAATCGAAGCATACGAACAAAAAAAAAGGAAGTAGAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTATCTATCCCCTCCACCTGGATGATCAAAATTGGACC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTGGGATCTGCGATCTCCAGTCCCAAAAAGTTCGC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCTCCCTACGCCCATTGATAATTAGATAGCACCC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CCAGGGTGCGATCTATTCTCCCATGAGAATTTCGGC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGTGATGTTTGTCAAGCTTTCGTTCAAAAGTGAGA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGTCGCACTTTCTGCCCTAGCATTTCGGCTTTAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GTTCTGGCGTTTTCGTAAGATTTTAAAAAATTATCG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCGCTCCCGTTCCCGACATTAGCCAACTGCGGAGCTC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGGGCTTGAGATGCCGCATTAGTAGTAGCAGCATA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TTGATTAATTGATTAGACATAGTTGATTGTTCCTTTTGAT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCACGAGGAGATTGACCCGGTAGGGGTGGAATCC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCAATAGGGGAGGATGTCAACGGCGGGAGAGTCCGA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATGGTTCCTGATTGGTCGAGTCTTTCGCAATTCCCGT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCATTTGCAACGTATCTTTAAAAGGTAAACACGAAGCC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CACTCTCCGGAAGCGCTCGACGGATCCCCCGAACCGT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CAGTAGAAGACTAAGCTGCTCGTATTTTGGGATGT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CCATCGGCGGCAATGTTGCTCCGGGGTCATGGGGAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGGACTCTCTCAGCCTCGGCCTTTGATGCAGCATA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATCATTTTTCTCCTGGTTGGGCGATCGTTTTTCGCGAT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATCGGATCTATCCACTCGATGGCCGCCGCTTGCCTC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TGAAGGCGTCTGTAGTGGTTTAAGTATAATGGGAAAAGA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TGTTGTATACTTTGGAACTTTTCCCAATGGTGGCTC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCGTCCAATCGACCTGAAACTCAACTCCTACCTAGG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCTTGGGACTTTCCGGCCTTCGGACGCGGTCTGGGTA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTGGGGCAGCTTTTCGAGTCGAAGCTCGGAAAGTCAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC

>NZ_CP051167|17|7|4026455-4029482|CRT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGTTCATTAATTCGGGGTCGAGTTCTATTAATAATT
CCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AATATATAAAACATAAAAAAGAAAGGGAATATATTGG
CCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CGATCGCGCGCCGACGGCGACAAAGAATAGGGC
CCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ACCCTTCAACCCTCCGGTAGCTCTGACGGTAGG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGGAATCCAATCCCGGCAGGCTCGGGGAGAGGCCTACGA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCATCTGGATACTCCGCACTGATTGGATCCCAAAT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGATCCCGACGAGTATTTTCTCTCATTCCAGGGAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGATTCCGACCTGTCTGGCACCAACCTCTCTGGGCGC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTACCCATTCTCCAATACTAGGGGTTACCGAGTA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CCTGTGCCTTACTCGTACTACGTCCACTATGGCTA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TGTCGAAAATCAACCTCTCTGGTCGCGACCTGAGC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTTAGGAATGGGCGCCATTTTTCGAGCTTGGCATT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CCAAAAAAATCCGAATCGTCGGTCACCGAGTAAGG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGAACGCGGTGTCCGGGACGGGAATCGCCGCACT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGTCATCCTCGGAGCCACCTGTCTGGGCATCCTCGG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATAATCGAAGCATACGAACAAAAAAAAAGGAAGTAGAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTATCTATCCCCTCCACCTGGATGATCAAAATTGGACC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTGGGATCTGCGATCTCCAGTCCCAAAAAGTTCGC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCTCCCTACGCCCATTGATAATTAGATAGCACCC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CCAGGGTGCGATCTATTCTCCCATGAGAATTTCGGC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGTGATGTTTGTCAAGCTTTCGTTCAAAAGTGAGA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGTCGCACTTTCTGCCCTAGCATTTCGGCTTTAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GTTCTGGCGTTTTCGTAAGATTTTAAAAAATTATCG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCGCTCCCGTTCCCGACATTAGCCAACTGCGGAGCTC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGGGCTTGAGATGCCGCATTAGTAGTAGCAGCATA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TTGATTAATTGATTAGACATAGTTGATTGTTCCTTTTGAT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCACGAGGAGATTGACCCGGTAGGGGTGGAATCC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCAATAGGGGAGGATGTCAACGGCGGGAGAGTCCGA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATGGTTCCTGATTGGTCGAGTCTTTCGCAATTCCCGT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCATTTGCAACGTATCTTTAAAAGGTAAACACGAAGCC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CACTCTCCGGAAGCGCTCGACGGATCCCCCGAACCGT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CAGTAGAAGACTAAGCTGCTCGTATTTTGGGATGT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CCATCGGCGGCAATGTTGCTCCGGGGTCATGGGGAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGGACTCTCTCAGCCTCGGCCTTTGATGCAGCATA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATCATTTTTCTCCTGGTTGGGCGATCGTTTTTCGCGAT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATCGGATCTATCCACTCGATGGCCGCCGCTTGCCTC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TGAAGGCGTCTGTAGTGGTTTAAGTATAATGGGAAAAGA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TGTTGTATACTTTGGAACTTTTCCCAATGGTGGCTC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCGTCCAATCGACCTGAAACTCAACTCCTACCTAGG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCTTGGGACTTTCCGGCCTTCGGACGCGGTCTGGGTA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTGGGGCAGCTTTTCGAGTCGAAGCTCGGAAAGTCAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC

>NZ_CP051167|17|12|4026456-4026926|PILER-CR
CTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGTTCATTAATTCGGGGTCGAGTTCTATTAATAATTC
CTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AATATATAAAACATAAAAAAGAAAGGGAATATATTGGC
CTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CGATCGCGCGCCGACGGCGACAAAGAATAGGGCC
CTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ACCCTTCAACCCTCCGGTAGCTCTGACGGTAGGG
CTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGGAATCCAATCCCGGCAGGCTCGGGGAGAGGCCTACGAG
CTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCATCTGGATACTCCGCACTGATTGGATCCCAAATG
CTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACGGATCCCGACGAGTATTTTCTCTCATTCCAGGGAGGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACAGATTCCGACCTGTCTGGCACCAACCTCTCTGGGCGCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCTACCCATTCTCCAATACTAGGGGTTACCGAGTAGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCCTGTGCCTTACTCGTACTACGTCCACTATGGCTAGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACTGTCGAAAATCAACCTCTCTGGTCGCGACCTGAGCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTTAGGAATGGGCGCCATTTTTCGAGCTTGGCATT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CCAAAAAAATCCGAATCGTCGGTCACCGAGTAAGG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGAACGCGGTGTCCGGGACGGGAATCGCCGCACT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGTCATCCTCGGAGCCACCTGTCTGGGCATCCTCGG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATAATCGAAGCATACGAACAAAAAAAAAGGAAGTAGAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTATCTATCCCCTCCACCTGGATGATCAAAATTGGACC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTGGGATCTGCGATCTCCAGTCCCAAAAAGTTCGC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCTCCCTACGCCCATTGATAATTAGATAGCACCC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CCAGGGTGCGATCTATTCTCCCATGAGAATTTCGGC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGTGATGTTTGTCAAGCTTTCGTTCAAAAGTGAGA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGTCGCACTTTCTGCCCTAGCATTTCGGCTTTAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GTTCTGGCGTTTTCGTAAGATTTTAAAAAATTATCG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCGCTCCCGTTCCCGACATTAGCCAACTGCGGAGCTC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGGGCTTGAGATGCCGCATTAGTAGTAGCAGCATA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TTGATTAATTGATTAGACATAGTTGATTGTTCCTTTTGAT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCACGAGGAGATTGACCCGGTAGGGGTGGAATCC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCAATAGGGGAGGATGTCAACGGCGGGAGAGTCCGA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATGGTTCCTGATTGGTCGAGTCTTTCGCAATTCCCGT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCATTTGCAACGTATCTTTAAAAGGTAAACACGAAGCC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CACTCTCCGGAAGCGCTCGACGGATCCCCCGAACCGT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CAGTAGAAGACTAAGCTGCTCGTATTTTGGGATGT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CCATCGGCGGCAATGTTGCTCCGGGGTCATGGGGAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGGACTCTCTCAGCCTCGGCCTTTGATGCAGCATA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATCATTTTTCTCCTGGTTGGGCGATCGTTTTTCGCGAT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATCGGATCTATCCACTCGATGGCCGCCGCTTGCCTC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TGAAGGCGTCTGTAGTGGTTTAAGTATAATGGGAAAAGA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TGTTGTATACTTTGGAACTTTTCCCAATGGTGGCTC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCGTCCAATCGACCTGAAACTCAACTCCTACCTAGG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCTTGGGACTTTCCGGCCTTCGGACGCGGTCTGGGTA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTGGGGCAGCTTTTCGAGTCGAAGCTCGGAAAGTCAG


>NZ_CP051167|17|13|4027251-4029482|PILER-CR
	GGTTCATTAATTCGGGGTCGAGTTCTATTAATAATTC
CTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AATATATAAAACATAAAAAAGAAAGGGAATATATTGGC
CTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CGATCGCGCGCCGACGGCGACAAAGAATAGGGCC
CTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ACCCTTCAACCCTCCGGTAGCTCTGACGGTAGGG
CTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGGAATCCAATCCCGGCAGGCTCGGGGAGAGGCCTACGAG
CTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCATCTGGATACTCCGCACTGATTGGATCCCAAATG
CTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACGGATCCCGACGAGTATTTTCTCTCATTCCAGGGAGGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACAGATTCCGACCTGTCTGGCACCAACCTCTCTGGGCGCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCTACCCATTCTCCAATACTAGGGGTTACCGAGTAGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACCCTGTGCCTTACTCGTACTACGTCCACTATGGCTAGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAACTGTCGAAAATCAACCTCTCTGGTCGCGACCTGAGCGCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTTAGGAATGGGCGCCATTTTTCGAGCTTGGCATT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CCAAAAAAATCCGAATCGTCGGTCACCGAGTAAGG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGAACGCGGTGTCCGGGACGGGAATCGCCGCACT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGTCATCCTCGGAGCCACCTGTCTGGGCATCCTCGG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATAATCGAAGCATACGAACAAAAAAAAAGGAAGTAGAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTATCTATCCCCTCCACCTGGATGATCAAAATTGGACC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTGGGATCTGCGATCTCCAGTCCCAAAAAGTTCGC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCTCCCTACGCCCATTGATAATTAGATAGCACCC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CCAGGGTGCGATCTATTCTCCCATGAGAATTTCGGC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GGTGATGTTTGTCAAGCTTTCGTTCAAAAGTGAGA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGTCGCACTTTCTGCCCTAGCATTTCGGCTTTAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GTTCTGGCGTTTTCGTAAGATTTTAAAAAATTATCG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCGCTCCCGTTCCCGACATTAGCCAACTGCGGAGCTC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGGGCTTGAGATGCCGCATTAGTAGTAGCAGCATA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TTGATTAATTGATTAGACATAGTTGATTGTTCCTTTTGAT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCACGAGGAGATTGACCCGGTAGGGGTGGAATCC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCAATAGGGGAGGATGTCAACGGCGGGAGAGTCCGA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATGGTTCCTGATTGGTCGAGTCTTTCGCAATTCCCGT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCATTTGCAACGTATCTTTAAAAGGTAAACACGAAGCC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CACTCTCCGGAAGCGCTCGACGGATCCCCCGAACCGT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CAGTAGAAGACTAAGCTGCTCGTATTTTGGGATGT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CCATCGGCGGCAATGTTGCTCCGGGGTCATGGGGAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	AGGACTCTCTCAGCCTCGGCCTTTGATGCAGCATA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATCATTTTTCTCCTGGTTGGGCGATCGTTTTTCGCGAT
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	ATCGGATCTATCCACTCGATGGCCGCCGCTTGCCTC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TGAAGGCGTCTGTAGTGGTTTAAGTATAATGGGAAAAGA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TGTTGTATACTTTGGAACTTTTCCCAATGGTGGCTC
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	TCGTCCAATCGACCTGAAACTCAACTCCTACCTAGG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	GCTTGGGACTTTCCGGCCTTCGGACGCGGTCTGGGTA
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC	CTGGGGCAGCTTTTCGAGTCGAAGCTCGGAAAGTCAG
GCTTCAATGGGGCTGTCCCAAAAAGGGACAGTGAAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168570098.1\|4013883_4015395_+\|threonine-ammonia-lyase,-biosynthetic	unknown	unknown	gnl\|CDD\|236417
NZ_CP051167.1\|WP_168570106.1\|4025013_4026192_-\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|274729
NZ_CP051167.1\|WP_168570115.1\|4044903_4046013_+\|AI-2E-family-transporter	unknown	unknown	gnl\|CDD\|223701
NZ_CP051167.1\|WP_168570109.1\|4032251_4034582_-\|type-I-U-CRISPR-associated-protein-Csx17	cas8u1	cd09767_cas8u1_CAS-I-U	gnl\|CDD\|274989
NZ_CP051167.1\|WP_168570112.1\|4038598_4039774_-\|GTP-binding-protein	unknown	unknown	gnl\|CDD\|223597
NZ_CP051167.1\|WP_168570116.1\|4046180_4047986_+\|PAS-domain-containing-protein	unknown	unknown	gnl\|CDD\|274362
NZ_CP051167.1\|WP_168570103.1\|4020695_4021730_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|315383
NZ_CP051167.1\|WP_168570099.1\|4015541_4017101_+\|DUF4070-domain-containing-protein	unknown	unknown	gnl\|CDD\|379101
NZ_CP051167.1\|WP_168570110.1\|4034585_4037069_-\|CRISPR-associated-helicase-Cas3'	cas3	cd09696_cas3_CAS-I-U	gnl\|CDD\|274235
NZ_CP051167.1\|WP_168570108.1\|4031311_4032262_-\|type-I-U-CRISPR-associated-protein-Cas7	cas7	cd09678_cas7_CAS-I-U	gnl\|CDD\|378223
NZ_CP051167.1\|WP_168570114.1\|4043380_4044847_+\|cysteine--tRNA-ligase	unknown	unknown	gnl\|CDD\|234705
NZ_CP051167.1\|WP_168570101.1\|4018636_4020007_-\|amino-acid-permease	unknown	unknown	gnl\|CDD\|273332
NZ_CP051167.1\|WP_168570100.1\|4017384_4018647_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570107.1\|4029733_4031284_-\|type-I-U-CRISPR-associated-protein-Cas5/Cas6	csb2gr5	cls000315_csb2gr5_CAS-I-U	gnl\|CDD\|274005
NZ_CP051167.1\|WP_168570111.1\|4037990_4038446_-\|D-tyrosyl-tRNA(Tyr)-deacylase	unknown	unknown	gnl\|CDD\|235383
NZ_CP051167.1\|WP_168570102.1\|4020230_4020686_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|224167
NZ_CP051167.1\|WP_168570105.1\|4023979_4024771_-\|HAD-family-hydrolase	unknown	unknown	gnl\|CDD\|223620
NZ_CP051167.1\|WP_168570104.1\|4021831_4023883_-\|magnesium-chelatase-ATPase-subunit-D	unknown	unknown	gnl\|CDD\|274135
NZ_CP051167.1\|WP_168570097.1\|4012226_4012733_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570113.1\|4040030_4043255_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340831

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168570098.1\|4013883_4015395_+\|threonine-ammonia-lyase,-biosynthetic	gnl\|CDD\|236417	PRK09224, PRK09224, threonine ammonia-lyase IlvA.	0
NZ_CP051167.1\|WP_168570106.1\|4025013_4026192_-\|alpha/beta-hydrolase	gnl\|CDD\|274729	TIGR03695, menH_SHCHC, 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate synthase. This protein catalyzes the formation of SHCHC, or (1 R,6 R)-2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate, by elmination of pyruvate from 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate (SEPHCHC). Note that SHCHC synthase activity previously was attributed to MenD, which in fact is SEPHCHC synthase. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	0.000131205
NZ_CP051167.1\|WP_168570115.1\|4044903_4046013_+\|AI-2E-family-transporter	gnl\|CDD\|223701	COG0628, yhhT, Predicted permease, member of the PurR regulon [General function prediction only].	3.28188e-51
NZ_CP051167.1\|WP_168570109.1\|4032251_4034582_-\|type-I-U-CRISPR-associated-protein-Csx17	gnl\|CDD\|274989	TIGR04113, hypothetical_protein_AaLAA1DRAFT_1703, CRISPR-associated protein Csx17, subtype Dpsyc. Members of this protein family are found exclusively in CRISPR-associated (cas) type I system gene clusters of the Dpsyc subtype. Markers for that type include a variant form of cas3 (model TIGR02621) and the GSU0054-like protein family (model TIGR02165). This family occurs in less than half of known Dpsyc clusters.	1.14684e-180
NZ_CP051167.1\|WP_168570112.1\|4038598_4039774_-\|GTP-binding-protein	gnl\|CDD\|223597	COG0523, COG0523, Putative GTPases (G3E family) [General function prediction only].	1.41305e-119
NZ_CP051167.1\|WP_168570116.1\|4046180_4047986_+\|PAS-domain-containing-protein	gnl\|CDD\|274362	TIGR02956, sensor_protein_TorS, TMAO reductase sytem sensor TorS. This protein, TorS, is part of a regulatory system for the torCAD operon that encodes the pterin molybdenum cofactor-containing enzyme trimethylamine-N-oxide (TMAO) reductase (TorA), a cognate chaperone (TorD), and a penta-haem cytochrome (TorC). TorS works together with the inducer-binding protein TorT and the response regulator TorR. TorS contains histidine kinase ATPase (pfam02518), HAMP (pfam00672), phosphoacceptor (pfam00512), and phosphotransfer (pfam01627) domains and a response regulator receiver domain (pfam00072). [Signal transduction, Two-component systems].	2.25867e-76
NZ_CP051167.1\|WP_168570099.1\|4015541_4017101_+\|DUF4070-domain-containing-protein	gnl\|CDD\|379101	pfam13282, DUF4070, Domain of unknown function (DUF4070). This is a bacterial domain often found at the C-terminus of Radical_SAM methylases.	5.68241e-69
NZ_CP051167.1\|WP_168570110.1\|4034585_4037069_-\|CRISPR-associated-helicase-Cas3'	gnl\|CDD\|274235	TIGR02621, CRISPR-associated_helicase_Cas3, CRISPR-associated helicase Cas3, subtype Dpsyc. This model describes a CRISPR-associated putative DEAH-box helicase, or Cas3, of a subtype found in Actinomyces naeslundii MG1, Geobacter sulfurreducens PCA, Gemmata obscuriglobus UQM 2246, and Desulfotalea psychrophila. This protein includes both DEAH and HD motifs.	7.49706e-65
NZ_CP051167.1\|WP_168570108.1\|4031311_4032262_-\|type-I-U-CRISPR-associated-protein-Cas7	gnl\|CDD\|378223	pfam09617, Cas_GSU0053, CRISPR-associated protein GSU0053 (Cas_GSU0053). This entry is found in CRISPR-associated (cas) proteins in the genomes of Geobacter sulfurreducens PCA and Desulfotalea psychrophila LSv54 (both Desulfobacterales from the Deltaproteobacteria), Gemmata obscuriglobus (a Planctomycete), and Actinomyces naeslundii MG1 (Actinobacteria).	1.12166e-57
NZ_CP051167.1\|WP_168570114.1\|4043380_4044847_+\|cysteine--tRNA-ligase	gnl\|CDD\|234705	PRK00260, cysS, cysteinyl-tRNA synthetase; Validated.	0
NZ_CP051167.1\|WP_168570101.1\|4018636_4020007_-\|amino-acid-permease	gnl\|CDD\|273332	TIGR00911, High-affinity_methionine_permease, L-type amino acid transporter. [Transport and binding proteins, Amino acids, peptides and amines].	3.16379e-47
NZ_CP051167.1\|WP_168570107.1\|4029733_4031284_-\|type-I-U-CRISPR-associated-protein-Cas5/Cas6	gnl\|CDD\|274005	TIGR02165, CRISPR-associated_protein_GSU0054_family, CRISPR-associated protein GSU0054/csb2, Dpsyc system. This model represents a CRISPR-associated protein from the Dpsyc subtype (a type I-C variant), named for Desulfotalea psychrophila LSv54. CRISPR systems confer resistance in prokaryotes to invasive DNA or RNA, including phage and plasmids. CRISPR-associated proteins typically are found near CRISPR repeats and other CRISPR-associated proteins, have low levels of sequence identify, have sequence relationships that suggest lateral transfer, and show some sequence similarity to DNA-active proteins such as helicases and repair proteins.	1.10487e-37
NZ_CP051167.1\|WP_168570111.1\|4037990_4038446_-\|D-tyrosyl-tRNA(Tyr)-deacylase	gnl\|CDD\|235383	PRK05273, PRK05273, D-tyrosyl-tRNA(Tyr) deacylase; Provisional.	5.08813e-85
NZ_CP051167.1\|WP_168570102.1\|4020230_4020686_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|224167	COG1246, ArgA, N-acetylglutamate synthase and related acetyltransferases [Amino acid transport and metabolism].	1.25008e-11
NZ_CP051167.1\|WP_168570105.1\|4023979_4024771_-\|HAD-family-hydrolase	gnl\|CDD\|223620	COG0546, Gph, Predicted phosphatases [General function prediction only].	2.10518e-27
NZ_CP051167.1\|WP_168570104.1\|4021831_4023883_-\|magnesium-chelatase-ATPase-subunit-D	gnl\|CDD\|274135	TIGR02442, Uncharacterized_protein_Rv2850c/MT2916, cobaltochelatase subunit. Cobaltochelatase is responsible for the insertion of cobalt into the corrin ring of coenzyme B12 during its biosynthesis. Two versions have been well described. CbiK/CbiX is a monomeric, anaerobic version which acts early in the biosynthesis (pfam06180). CobNST is a trimeric, ATP-dependent, aerobic version which acts late in the biosynthesis (TIGR02257/TIGR01650/TIGR01651). A number of genomes (actinobacteria, cyanobacteria, betaproteobacteria and pseudomonads) which apparently biosynthesize B12, encode a cobN gene but are demonstrably lacking cobS and cobT. These genomes do, however contain a homolog (modelled here) of the magnesium chelatase subunits BchI/BchD family. Aside from the cyanobacteria (which have a separate magnesium chelatase trimer), these species do not make chlorins, so do not have any use for a magnesium chelatase. Furthermore, in nearly all cases the members of this family are proximal to either CobN itself or other genes involved in cobalt transport or B12 biosynthesis.	0
NZ_CP051167.1\|WP_168570103.1\|4020695_4021730_-\|hypothetical-protein	gnl\|CDD\|315383	pfam12695, Abhydrolase_5, Alpha/beta hydrolase family. This family contains a diverse range of alpha/beta hydrolase enzymes.	3.26293e-06
NZ_CP051167.1\|WP_168570113.1\|4040030_4043255_-\|glycosyltransferase	gnl\|CDD\|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	5.77677e-38

>NZ_CP051167.1|WP_168570106.1|4025013_4026192_-|alpha/beta-hydrolase
MTNTDSFVTPTEEQLRRTKEAINAYLETIARHGDRREWAYPYYLFHDPGKPIRGTVMMFHGFSAKPHQMWRLADYLFHNGFNVYQTTLAGHHLLPPHQYWPQVDLKPEIYDPLRKKVKKDPVLNQFFNNISDNPSGFTQPSALQQKALLARLLILEPRLLNIMQAIEREDEDEFDRYFNSSHEDYLTCASQRLHEISELPGPVYAVGLSVGGAVALAVAANHPETVKGVVAYAPLLKIYGDRRRYVNLAGPLDIAELGWDPQLKFPVGCLTAADRFGRTAVLNSKAIAALQNIPTFLVLTENEDAADIETNQMLFDKIGGEAGGHRSYFYPASDLVPHPMVDPTEISQGMSNRFWRSLYQETLRFLTKGEIDADNMGNVEQDPDLPPVPDAN
>NZ_CP051167.1|WP_168570105.1|4023979_4024771_-|HAD-family-hydrolase
MKPTRPYLTPYSPSVKTEGPLADWTVFCDFDGPLIDVSERYYSTYRLGLAKTEAVYQARSQKLPLQILSKEQFWQMKRDRVPDVEIARQSGLDDEQTDVFLGQVHEIVNQPHLLHKDRLQPGVRWALGLLHCQGARLVSVTLRHQDQVTDILEKTGLAPLFSGIWGTDDLALAYQNYAEVKTHLLAEAIAEHGVDRDRACIIGDTEADILAAKAVGIPSIAVTCGIRSANYLSQFKADRTYSDLVDAAHALLQNALCPQICAC
>NZ_CP051167.1|WP_168570104.1|4021831_4023883_-|magnesium-chelatase-ATPase-subunit-D
MPAPVTRSNLTTFPLTAVVGQEAIKMALLLTAVDPGLGGVAIAGRRGTAKSVMARAIHSLLPPIEIVKDSIANCDPTHPEEWDDYTLETYPRNAQNGVSATDSVPTEIIPTPFIQIPLGTTEDRLLGSVDVEQSVKQGETVFQPGLLASAHRGVLYVDEINLLDDQIANLLLSVLTDGRNQIEREGISFQHPCKPLFIATYNPEEGPLREHLLDRIAITLSADGVLGLDDRVMAVEQALSYANSPQTFLDQYAEDLENLKTQILLAREWLKDVVISHDQIAYLVDEAVRGGVQGHRAELFAVRVAKASAALDGRNTVNADDLRRAVELVIVPRSTIVQTPPEEEQPPPPPPPPPPPPEGEQEQEQEEEEEQEEEEPPEQEEQEQSIPEEFVFDPEGVIIDPAMMYFAQMAKRKGKSGARSIIFSEDRGRYIKPMLPKGQVKRVAVDATLRAAAPYQKARRERYPGRKVIVEQSDLRSKRMARKAGSLVVFLVDASGSMALNRMQSAKGAVLQLLTEAYQNRDQIALIPFRGEQAEVLLPPTRSITTARRRLERMPCGGGSPLAHGLTTAVRVGMNAQQSGDIGQVLIVAITDGRGNIPLARSLAEPMEEGEKPDLKAELLEIAGKIRLAGMQLLVIDTENKFISTGFGKELAKQAGGKYYHLPKATDQALAAMAKGAIADAKR
>NZ_CP051167.1|WP_168570103.1|4020695_4021730_-|hypothetical-protein
MSRLFALGAIAALAAVSVTLVPHFLANSQPVERPSEPAIAPVAIETPSPVPMQTDRDPSQPLYAKVDRFKTTIPGYNDPADIYYPQPSQLAPADRLPVALLIQGFNVDAAYYSQFATQIARYGFIVVVPNHLTTIRDREELFPQVGQVTDVLRYVKAQQHHANSPLFKITDAEKLVLIGHSQGGFIGLDAIREACDLPWCEGPYERPKELLAGVFFGSDLWEDGEYLKVNNAGIPIALIAGSRDSLIRAESIEKTYNNIESPPKAYIEVRGANHYGLTDLDNPPGSPNEKSSSTLDRAVSLETIARWTAVFLRAYALDDRAALAYLGDRGPREDPNVRVRWQGN
>NZ_CP051167.1|WP_168570102.1|4020230_4020686_-|GNAT-family-N-acetyltransferase
MTDALPPGCTLRRARKSDIWTIRRLVFSEKLDPTQLDWRQFWAIEFEGKTIACAQLRSIDGVRELGSLVVVPSWRDRGLGSYLVRHLVEGTSEPIYLECMGYLAPFYARLGFVEIGWRSLPKPLKVKFGLGQFASRFLPIEVKIMQYIHRE
>NZ_CP051167.1|WP_168570101.1|4018636_4020007_-|amino-acid-permease
MKADSNRSSRLIGPFTAICLVVANTIGTGVFTSLGYQVADIQSYFALLALWAIGGIFAMCGALSYAELGSVMPRSGGEYTFLSQIYHPAIGFLSGWISVTVGFAAPIAAAAIALADYLSQVFPIPNETLVAAIVAILISTIHTRNLKTGSSFQDWFTVLKVISIVVLIACGFFLAEPQFVNLLPSAGDIQPIFSPPFAVSLVFVTYAYSGWNASVYIANEIDKPEKNLPFSLIVGTAIVMVLYLLLNFIFLYSTPLQALAGKTQVGAIAAEYIFGDFGGKLMSLLISFGLISSISSMIWAGPRVTQAIGEDIPFFQPLAKKNASGIPDLAIWIQLSLILVLLITSTFEALVTYLGFTLTLSSLMTVAGVFVHRYKYPQISRPYQTWGYPITPLIFVGVGLWVLIFTLMGKPVESLAGLFTIFLGLPIYFFAARKKLVSSSDLRSSKQSISKNYDET
>NZ_CP051167.1|WP_168570100.1|4017384_4018647_-|hypothetical-protein
MKPKTSQFSSFFLSIFGLLLLVQGCANTSTPVASESAQVSSQTSTEVTPEGEGRQEVSAAEIKASETKADPAPKIDRAKADKLTGNAKFIAGIKVEKEGAIAELQKSNAWLNYSQTLDNSWSALEAQQLSKVRRWSDKQLQSIQANAPTIFYPFSGPDFLYAYSLFPQGSNYIMVGLEPLGSIPDFENMSEGAKAQKLQEIQQSLYAILQFSFFRTKSMAQDLAEKGVIPILLFFMARTNNEVVDIQYVGIDESGEARSLDDIGDNTNAIPGVKIAFIPEGETEPRSLYYFSTDLSNSGLANTPQFEKFVKQFDNPITYLKAASYLMYNESFSQIRDLIFAQSSHILQDDSGIPLRNFDREQWELDFYGTYIAPIDLFKNRYQPELREIYQSDSSIEPLDFGIGYKYYQDSNLMLATRTN
>NZ_CP051167.1|WP_168570099.1|4015541_4017101_+|DUF4070-domain-containing-protein
MRALLIYPLFPPTFWSYNKILELVDRQVLLPPLGLITVAAILPQTWEFKLVDRNVREVTQAEWDWADLVILSAMIVQQEDLTAQIREAKQRGKLVAVGGPYPTSVPEDSERAGADFLILDEGEITLPMFVEAIEKGATSGIFRTSEKPDVTQTPIPRYDLLELDAYDSMSVQFSRGCPFQCEFCDIIVLYGRKPRTKTPTQLLEELAYLYNLGWRRGIFMVDDNFIGNKRNVKLLLKELKIWQANHQYPFRFNTEASVDLAADPELMELMVQCNFDAVFLGIETPDEESLQLTKKFQNTRDSLTETVGKIIEAGLRPMAGFIIGFDGEKKGASDRIVQFVEDAAIPTAMFGMLQALPNTALWQRLEKEGRLRIHGKQDINQSTLMNFEPTRPMEDIAREYIEAFWELYEPETFLDRTYRCFLKLGAPQCKAPFKLPSWVDIRALAIVIWRQGVKRKTRWKFWHHLFGIFRHNPAVWEHYLTVCAHNEHFLEYRQIVRDEIQNQLALFQEQEARTEMAIG
>NZ_CP051167.1|WP_168570098.1|4013883_4015395_+|threonine-ammonia-lyase,-biosynthetic
MYSDYLTRILNARVYDVAQESPLEYAPNLSARLHNQLLLKREDMQSVFSFKLRGAYNKMAQLPPDLLAQGVIAASAGNHAQGVALGASRLGTRAIIVMPVTTPQVKVDAVNARGGEVVLHGETYDDAYAYARQLESEKGMTFIHPFDDPDVIAGQGTIGMEILRQYQKPIHAIFVAIGGGGLIAGVAAYVKRLRPEIKVIGVEPVDADAMHQSLKAGYRVRLPQVGLFADGVAVRSVGKETFRLCQQYIDDIILVGTDDTCAAIKDVFEDTRSIVEPAGALAIAGAKAYVEREQIEGQTLVAIACGANMNFDRLRFVAERAELGERREAIFAVTIPETPGSLRKFGECIGKRNLTEFNYRIADEKEAHIFVGMQIQNRADAAKMVETFQANGFKTIDLTDDELTKLHLRHMVGGRSPLAHNELIYRFEFPERPGALLKFVSSMSRNWNISLFHYRNNGSDYGRIVVGMQVPPEEMEEWQAFLNSLDYRYWDENQNPAYKLFLA
>NZ_CP051167.1|WP_168570097.1|4012226_4012733_+|hypothetical-protein
MSRRFRNPHPIARFVQRLARSLLYLFGELTIYLTILAVTALLVAWGLSVKIALGIGITLSGLVAIVSFWAYRQHRLAIGRSRDRDAPSLHGDVKFADWIAQTLARKAPREWEEYQDWLHDILLARRQMLDEGDRPWQVTALTYGRLIALCVTVARIKLRRWAMLLQRR
>NZ_CP051167.1|WP_168570107.1|4029733_4031284_-|type-I-U-CRISPR-associated-protein-Cas5/Cas6
MSVTLSIRFLTGRFHATPWNHQVNEGIVEYPPSPWRILRALVSAYYYLSDRPPRDRLCQLVTQLADSLPSYRLPPHTTAHTRHYMPLRKEGKETTTKVLDTFVVFDRATTIPEKAPEIQVVWHDVELDDKQRQLLECLCHQLTYLGRAESWCEVSPCYTTATACNARPLGAYEVAAGETTRILVPLSQSEFEGFKTALGNVERPKRAKWRIPQDLLDTLEVDIGELHRQGWSGVPGARWATYTIANNSNNVRGWSVTERQAIARPTLARFDLSSNVLPPLTEALAVGERFRQTLMSRSDDGSQAMETFSGRRKTGEKRQNQRHAWYLPEDSDGDGRIDRLWVFAAEGFGEDAVRVLCGLSKVWAGKAFEVQTRLTGLGTLEDYRSTTIRQSRSLLGCSRIWRSLTPFVLPRHPKKKIDPDTGWQVDGVQWQAKHLIDHLRSVWAIAPLADVRVLSDSDIDCPYPWHAFRRRRSSGKGHQSSDRGYWIELEFEKEQCGPIAIGYGAHFGLGLFVPDL
>NZ_CP051167.1|WP_168570108.1|4031311_4032262_-|type-I-U-CRISPR-associated-protein-Cas7
MDFKALENTNRLLIEADLKPLQGTRFQPTGFPDLGAATYQLPDTNRTEMVLLESAQSVANRLENTIWDEAAQDVIEPLRGISYVVVKQDGEVLTNSLLEAHRINSFYLLEGKDKSFLNDLKSELDALDKKGAIDPHKLAVTLAKYDINSLLHGVFLAKKELAGGRFRLARALSGFIEAYNVRPVQFGGVKLDRVDPKAEAKKGGGNIPYARTEYTAEAITAFFSLDLAQLRNYRLGDDATDLLIAIALYKIRSFLEDGLRLRTACDLECTDIRVTRPEKFTLPKRDELTTLLPKLVKAARPLFDDEPVRVVQYKEA
>NZ_CP051167.1|WP_168570109.1|4032251_4034582_-|type-I-U-CRISPR-associated-protein-Csx17
MDLALPGARPDSVASYLKALGILRLLHEQHRARMKGSWQRQVVVQESSWMASFEASPDGNIESDVFVLTGAIAADELVNFFLCEYEPTPILSPWNGSTGFYPKDNKKTLDAVRQSQTKRLTAYRETIAIAQQIVNEMGLKKQPSGDDKNKLIRQLRDRLPDLAVRWIDTCALVSNDDIQYPPLLGTGGNDGNFEFSRTFQQQLQNLIDFKTGKPTADAETLLKAALFGETLPGLSFSGKIGQFDPIAAGGANAAPGFEGKSRVNPWDFVLMVEGTLTFQARLTRKFESSTHGALTYPFAVRPTPMGYGTAAEDENIRAETWMPLWSRPTRFDELHVFFGEGRAKVGERHKTGVDFALAVADLGKFRGIDAFVRYSFQERNGLSYFAVPLGEFRPRDRSGDSSTTNLLSPILPWLDRFRRVAEPKEAPAAIKRVHRLLETRIVEFAQAEAQPGARGNNALAVLVALGEVEQTLDRSLTWVREVHLPPIPWLRSRWVEACNDDSVEFHLALALAGRGLYRKVVDDPETQLPRLIDYPEPDRGLRQRLVRVRGSQSKPSWKDSDAITVWQGGTLTDNLLILLRREEIEAQQGQKQESAQDADPTNSHSHSSSHPATARLRDIQAWIDGTVDDRRLEAIARGLALVKRHRSTQGKDSREEINAVPAAFALLEPVVRRVVPAPTEEGTLSKDSKIVLPRVSGLWSRLEVGDCQTATELAIRRLRASRFRLAVRPFELRRDRTRRIAAALAFPIAEETSRQLLDRICYRIVENKEEKKEDGL
>NZ_CP051167.1|WP_168570110.1|4034585_4037069_-|CRISPR-associated-helicase-Cas3'
MKFSEFFQIATGKPPFPYQERLACADKLPLVLNVPTGSGKTATVVLGWLWRRQHDRDRTPRRLVYCLPMRSLVEQTERSIHKWLDHLKGRNALDEDIKDIEVHKLMGGSVSHDWDDRLDRNTILVGTQDQLLSRALNRGYAMSRYRWPVHFAQLNNDCFWVIDETQLMGAGLRTTAQLQWLREHFSTYGTARTLWMSATLDSDILKTVDYRQTYGNLDRPFTLGEDDREHPTLQKRLSASKSIQRTAIVVPSKGGDKEVRQYARKLTSTIAEVHRADTLTLIVCNRVDRARAVYRELQQLQRKGEIDAEIGLIHSRFRAGDRQTLGARYLDDEHPFRGILVATQVVEAGVDISATTLFTELCPWSSFVQRLGRCNRYGEATEAAVYWIDFDKKVDDKATSPYRAEAIEQARYLVGQLQEQQGNAGIESLQTFLENLPDDKRSPQALEGMVLRRHDLMQLFDTASDLAGHDIDISPFVREAQDNNVEIAWRDWGKGNPSADWGDENYVGKLYRDELCRVSMAQAQQFLKQREAWTFDAPNKQWRKVAHNELFPGITLLVRTTDGGYSSELGFTGGKEKDFAPLDLPEDGDFNSDRDDPLSQVGTYITLEQHARDTFNEAQKLCEALKLSDLPVESIARAARYHDAGKAHEEFQKMLTWNREERKGATLWAKSDRDFKNSSDRPPRKFQDRGFRYLRHEWASALLALQQGEPFLLAYLVACHHGKVRMVVQPYPNEKAAPHGKAYARGVWDGDTLPEIDLGDGLTIPSCQLSLDCVALGENSDGEPSWVARSLDLLDEYGAFKLAYLETVVRVADWRASARYTGPLAEE
>NZ_CP051167.1|WP_168570111.1|4037990_4038446_-|D-tyrosyl-tRNA(Tyr)-deacylase
MRVIIQRVKSSQVMVGDRAIGQIGKGLNLLVGIAETDTEAELDWMARKCLELRLFPDETSDRARWDKSVLDIRGELLVVSQFTLYGDCRKGRRPSFDRSASGDRAQQLYEQFVGKLRQSGLKVETGEFGAMMHVAIDNDGPVTLILEREAD
>NZ_CP051167.1|WP_168570112.1|4038598_4039774_-|GTP-binding-protein
MQTTDTSHAESPTMEAPKHGLPVTIITGFLGSGKTTLLNHILANQEGLKTAVLVNEFGEIGIDNELIVSTGDDMVELSNGCICCTINNDLLDAVYKILERSDRVDYLVVETTGLADPLPVALTFLGTELRDLTRLDSIVTLVDSENYSLDLFNSQAAYSQIAYGDIILLNKVDLVDEADVDLLESKIRDVKADARILRTTRSQVPLPLILSVGLFESDKYFTPEKSAESHDHHHHHDHDHHDHHDHHDHHDHSDCDHDHGHCVHDHDHDHHDHDHHDHHHHSDHLAMDGFTSLSFQSDKPFAIRKFQYFLDNQLPSTIFRAKGILWFDESDRRHIFHLSGKRFSIDDDDWNTEPKNQLVLIGQNLDHDKLREQLNKCLCLPSSNSGKGFGR
>NZ_CP051167.1|WP_168570113.1|4040030_4043255_-|glycosyltransferase
MTRFAENSNDKNPAKMRILVEGWRFIPHSYAIINHFQLLQLRRRPEVELFHRDRPFVKGSDWKPASGLLDEAAEATIRAIAEPPPGWVPDATLRMYCPFDLTPAPSGRTLVFGCTEWGIVTRYILRAMGVDSFQKAHGDNDTVIVTSSRWSRDGFVRSGADRDRVKVVPLGVDPTIYQPVTPAKKREIRRKFGWEEDCFLFLNVGVMWNERQGIDMLLKAFAAICDRHPEARLVLKGRDAIFPSRDSIVRASRQVLSERELQKIAPRLIYIGESLSCAQMAQLYQAADAYVSPYLAEGFNLPVLEAIACGLPVICTDGGPTDDFIRDEFALRIASQLKNPWREKERVFVVMPQFDSLVAHMERAIADAALRARSHDFGPRWVRDRFTWKQTIDRLLPLFDPAMTLDPTTVPPEIAQSEIAQSEIAQSEITQSEITLSGITSVRPSQSIIVEGWRFLPHSYAIANHYHLLEMSDRPNLQVFHRDAPFPTRDARSIADMVDRATGDRLRAIPPPPPDLFADTTLRIFSPLNLREAPNSRKTCVFGTTEWGIVHPQLLLLHDRAPLSEILDRTNTLIITPSNWSREGFLRSGAPGDRVTVVPHGVDPNLYHPVSEDERESLRRQLGWDGQFIFLNIGAMTAEKGIAPLLFAFAQIAETHPQARLVLKGSDAIYSSDESIRRVCEKTLDRRQAEIVRDRLIYIGTTLSASAIVRLYRAADVYVAPYLAEGFNLTVLEAIACGLPVICTRGGPTDDFTRPEFTWYIESQLETITKFGDLRYARSPNWDSLIALMERAIASPEFRLQARSSGPAFVGDRFTWRRVVDRLLEVILPDRAGDYTDDTAKPSLRERPPAIGQYSQYTDPTPAPPPHPPASYGVPADLTGKRVLELGTTQGYWSFEALRRGAREAIAANLQIEGVTAPFDRQCFDNYRRIRAFDPSVCSYRDLSLDALDPNQLGYFDVIFLFGTCDRVRYPLLLCDRLATLCRGELYLEAAILDDYSRDRGGLGCGYPGSQMLLEFNPNSTTNNPSQPLWRPTLYALAQLVKSAGFTQVKAWKLTDSPQTEPQCRGFVVGSHLG
>NZ_CP051167.1|WP_168570114.1|4043380_4044847_+|cysteine--tRNA-ligase
MTLKLYNSLTRRQEPFEPVESGKVRMYCCGVTVYDYCHLGHARSYIAWDTVRRYLIWRGFDVRYVQNFTDIDDKILNRAREQGTSMEEVADRYTQAYFEDMDRLNILRADDYPRATHTLNGIERLISELEQKGYAYPAGGDVYYAVRKFPEYGQLSGRKLEEMQAGASGRVAEDDPDKNKKKDPFDFALWKAAKPGEPAWDSPWGKGRPGWHIECSAMVREKLGETIDIHMGGADLVFPHHENEIAQSQAATGHPLAKYWMHNGFVTVNGEKMSKSLGNFTTIRELLDRPTDPMAVRLFVLQAQYRKPIDFTEEAIATAEKGWATLKEGLSFGFQFGARLGWETSELPPASQLDAGAIARFEQAMDEDFNSPGAIAVLFELAKELRRQGNLLVHEGEIQGDSQRVQKQWQTLVSLAGVLGLKVDADAELSPTPSDGLSDEAIAALLERRQAARQAKDFAEADRIRDELQAQGIVTIDRPGGVTQWHRS
>NZ_CP051167.1|WP_168570115.1|4044903_4046013_+|AI-2E-family-transporter
MSVPRLRISLTNPVLIAIVGLILVLMWQVRSLLVTLMISVVLAASISPVVNWAEKYRIPRWLATLATYLILIAGLTGAGLAIGPAVASQIERLVRQLPVYLETLREIAEDLAANFNDTPPEFVRQFFDTQSLTTWAIRSSQQLLLRSYGLTRGFVGGVVSLILSLFISGYMVADSRTLINSVVQLFPSPWDRNLEAQIEPISYRMGGYIRGRLLVSAILGVAITAGLTLLGLGDFALGLGAIAGVTNLIPFLGPVLGAIPALIVAISQGSWTFLWVLILFVIIQNVETYILDPLLVGSSVGVHPLYQLLSVLGGVQVLGIIGAIVVPPWFAGVSALVENLYLKPKLMAQNNGENTETDEVGAIASDESR
>NZ_CP051167.1|WP_168570116.1|4046180_4047986_+|PAS-domain-containing-protein
MGHWPKFGKLTPTKIVAIYALVGSLWILFSDRVIALILQNPEFDRLTQFQTVKGWVYVIVTALLLDRLIRRYATILNRSREQLKRSEERLEAIVETTTSGIVVLDTEGRITLSNQAAAHLLGYPRSATLGGVDERSPQSMQRSTYPTLAEIVPFDRVRETGQPSCAIEYEIHYPDRPPAILSIDTAPLYDGEGRFEGAVVAIADISERKHAEAIARARDLAEARNRAKSEFLAQMSHEIRTPLNGVLGLSQILQREIFGPLNPKQREYINRIKDSGDHLLELINDILDLSKIEAGKAQLQYSAIEVAQLCKYCLKIVQERAYERGLQLTTDIDPQVRTLVGDERRLKQILLNLLSNAVKFTPEGQVSLRVEKTPPGLRITVADTGIGIAPEDLPLVFEPFHQIQNDLNAKTQGTGLGLALSRDLARLHGGDLDAESTPGQGSRFHLYLPDLPSGYLPPEPSEEADRVDLTTDLSRRTGRVAIVEPDRSTEILLRDYLQALGCEIEIVTDSDRLFEESAEIVPDLILLDVSWSNFSRRQQWLSQLRDRAAWQGIPAIAIAAMAMAGDRDRVLEAGATDYLTKPIQLEQLDRLLLQYLPGAGR

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Crispr_ID: NZ_CP051167_18

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_18

4105374-4105521

Orphan

N:A

Consensus_repeat	Method
CCTTTCAAAGGGGGGCGAAGGAGGGATTTTGGGGGGAACGAGGAAAG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051167_18

>merge|NZ_CP051167|18|4105374-4105521|CRISPRCasFinder
CCTTTCAAAGGGGGGCGAAGGAGGGATTTTGGGGGGAACGAGGAAAGATCTCGCCATGGGATTGGCGCAAAGGAAAACGATCCCCCTATCCCCCCAACCCCCCTTTGAAAGGGGGGCGAAGGAGGGATTTTGGGGGGAACGAGGAAAG

>NZ_CP051167|18|16|4105374-4105521|CRISPRCasFinder
CCTTTCAAAGGGGGGCGAAGGAGGGATTTTGGGGGGAACGAGGAAAG	ATCTCGCCATGGGATTGGCGCAAAGGAAAACGATCCCCCTATCCCCCCAACCCC
CCTTTGAAAGGGGGGCGAAGGAGGGATTTTGGGGGGAACGAGGAAAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168570162.1\|4115948_4116704_-\|peptidylprolyl-isomerase	unknown	unknown	gnl\|CDD\|223831
NZ_CP051167.1\|WP_168570157.1\|4096506_4097367_+\|calcium-binding-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570158.1\|4097423_4105163_-\|CHAT-domain-containing-protein	unknown	unknown	gnl\|CDD\|227328
NZ_CP051167.1\|WP_168570155.1\|4093707_4094628_+\|NAD(+)-kinase	unknown	unknown	gnl\|CDD\|179455
NZ_CP051167.1\|WP_168570151.1\|4090576_4091695_+\|NADH-quinone-oxidoreductase-subunit-NuoH	unknown	unknown	gnl\|CDD\|214341
NZ_CP051167.1\|WP_168570154.1\|4093202_4093508_+\|NADH-quinone-oxidoreductase-subunit-NuoK	unknown	unknown	gnl\|CDD\|176958
NZ_CP051167.1\|WP_168570163.1\|4116967_4117153_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570156.1\|4094749_4096405_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340825
NZ_CP051167.1\|WP_168570159.1\|4105739_4107704_-\|calcium-binding-protein	unknown	unknown	gnl\|CDD\|380205
NZ_CP051167.1\|WP_168570149.1\|4088388_4088895_+\|phosphohistidine-phosphatase-SixA	unknown	unknown	gnl\|CDD\|224973
NZ_CP051167.1\|WP_168570164.1\|4117215_4119765_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|366154
NZ_CP051167.1\|WP_168570150.1\|4089058_4090219_+\|citrate-synthase	unknown	unknown	gnl\|CDD\|237591
NZ_CP051167.1\|WP_168570167.1\|4128144_4128693_+\|dTDP-4-dehydrorhamnose-3,5-epimerase	unknown	unknown	gnl\|CDD\|376414
NZ_CP051167.1\|WP_168570152.1\|4091810_4092434_+\|NAD(P)H-quinone-oxidoreductase-subunit-I	unknown	unknown	gnl\|CDD\|129498
NZ_CP051167.1\|WP_168570160.1\|4108731_4110945_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|226428
NZ_CP051167.1\|WP_168570166.1\|4123910_4127777_-\|response-regulator	unknown	unknown	gnl\|CDD\|274362
NZ_CP051167.1\|WP_168570165.1\|4120000_4123870_-\|response-regulator	unknown	unknown	gnl\|CDD\|274362
NZ_CP051167.1\|WP_168571930.1\|4112982_4115955_-\|type-I-secretion-system-permease/ATPase	unknown	unknown	gnl\|CDD\|225183
NZ_CP051167.1\|WP_168570161.1\|4110990_4112787_-\|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|130902
NZ_CP051167.1\|WP_168570153.1\|4092510_4093131_+\|NADH-quinone-oxidoreductase-subunit-J	unknown	unknown	gnl\|CDD\|214335

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168570162.1\|4115948_4116704_-\|peptidylprolyl-isomerase	gnl\|CDD\|223831	COG0760, SurA, Parvulin-like peptidyl-prolyl isomerase [Posttranslational modification, protein turnover, chaperones].	2.77631e-16
NZ_CP051167.1\|WP_168570158.1\|4097423_4105163_-\|CHAT-domain-containing-protein	gnl\|CDD\|227328	COG4995, COG4995, Uncharacterized protein conserved in bacteria [Function unknown].	1.54189e-85
NZ_CP051167.1\|WP_168570155.1\|4093707_4094628_+\|NAD(+)-kinase	gnl\|CDD\|179455	PRK02645, ppnK, NAD(+) kinase.	0
NZ_CP051167.1\|WP_168570160.1\|4108731_4110945_+\|tetratricopeptide-repeat-protein	gnl\|CDD\|226428	COG3914, Spy, Predicted O-linked N-acetylglucosamine transferase, SPINDLY family [Posttranslational modification, protein turnover, chaperones].	1.27372e-78
NZ_CP051167.1\|WP_168570154.1\|4093202_4093508_+\|NADH-quinone-oxidoreductase-subunit-NuoK	gnl\|CDD\|176958	CHL00015, ndhE, NADH dehydrogenase subunit 4L.	1.08516e-51
NZ_CP051167.1\|WP_168570165.1\|4120000_4123870_-\|response-regulator	gnl\|CDD\|274362	TIGR02956, sensor_protein_TorS, TMAO reductase sytem sensor TorS. This protein, TorS, is part of a regulatory system for the torCAD operon that encodes the pterin molybdenum cofactor-containing enzyme trimethylamine-N-oxide (TMAO) reductase (TorA), a cognate chaperone (TorD), and a penta-haem cytochrome (TorC). TorS works together with the inducer-binding protein TorT and the response regulator TorR. TorS contains histidine kinase ATPase (pfam02518), HAMP (pfam00672), phosphoacceptor (pfam00512), and phosphotransfer (pfam01627) domains and a response regulator receiver domain (pfam00072). [Signal transduction, Two-component systems].	2.95204e-71
NZ_CP051167.1\|WP_168570156.1\|4094749_4096405_+\|glycosyltransferase	gnl\|CDD\|340825	cd03794, GT4_WbuB-like, Escherichia coli WbuB and similar proteins. This family is most closely related to the GT1 family of glycosyltransferases. WbuB in E. coli is involved in the biosynthesis of the O26 O-antigen. It has been proposed to function as an N-acetyl-L-fucosamine (L-FucNAc) transferase.	7.44358e-13
NZ_CP051167.1\|WP_168570159.1\|4105739_4107704_-\|calcium-binding-protein	gnl\|CDD\|380205	NF033203, entero_EhxA, enterohemolysin EhxA. Members of this family are the RTX toxin called enterohemolysin or EhxA, because it is found in enterohemorrhagic Escherichia coli (EHEC) strains such as O157:H7.	1.85177e-12
NZ_CP051167.1\|WP_168570149.1\|4088388_4088895_+\|phosphohistidine-phosphatase-SixA	gnl\|CDD\|224973	COG2062, SixA, Phosphohistidine phosphatase SixA [Signal transduction mechanisms].	6.12323e-44
NZ_CP051167.1\|WP_168570164.1\|4117215_4119765_+\|glycosyltransferase	gnl\|CDD\|366154	pfam00535, Glycos_transf_2, Glycosyl transferase family 2. Diverse family, transferring sugar from UDP-glucose, UDP-N-acetyl- galactosamine, GDP-mannose or CDP-abequose, to a range of substrates including cellulose, dolichol phosphate and teichoic acids.	4.49366e-29
NZ_CP051167.1\|WP_168570150.1\|4089058_4090219_+\|citrate-synthase	gnl\|CDD\|237591	PRK14036, PRK14036, citrate synthase; Provisional.	0
NZ_CP051167.1\|WP_168570167.1\|4128144_4128693_+\|dTDP-4-dehydrorhamnose-3,5-epimerase	gnl\|CDD\|376414	pfam00908, dTDP_sugar_isom, dTDP-4-dehydrorhamnose 3,5-epimerase. This family catalyze the isomerisation of dTDP-4-dehydro-6-deoxy -D-glucose with dTDP-4-dehydro-6-deoxy-L-mannose. The EC number of this enzyme is 5.1.3.13.	6.65519e-112
NZ_CP051167.1\|WP_168570152.1\|4091810_4092434_+\|NAD(P)H-quinone-oxidoreductase-subunit-I	gnl\|CDD\|129498	TIGR00403, NADPH-quinone_oxidoreductase_subunit_I, NADH-plastoquinone oxidoreductase subunit I protein. [Energy metabolism, Electron transport].	1.01676e-117
NZ_CP051167.1\|WP_168570151.1\|4090576_4091695_+\|NADH-quinone-oxidoreductase-subunit-NuoH	gnl\|CDD\|214341	CHL00032, ndhA, NADH dehydrogenase subunit 1.	0
NZ_CP051167.1\|WP_168570166.1\|4123910_4127777_-\|response-regulator	gnl\|CDD\|274362	TIGR02956, sensor_protein_TorS, TMAO reductase sytem sensor TorS. This protein, TorS, is part of a regulatory system for the torCAD operon that encodes the pterin molybdenum cofactor-containing enzyme trimethylamine-N-oxide (TMAO) reductase (TorA), a cognate chaperone (TorD), and a penta-haem cytochrome (TorC). TorS works together with the inducer-binding protein TorT and the response regulator TorR. TorS contains histidine kinase ATPase (pfam02518), HAMP (pfam00672), phosphoacceptor (pfam00512), and phosphotransfer (pfam01627) domains and a response regulator receiver domain (pfam00072). [Signal transduction, Two-component systems].	5.49802e-64
NZ_CP051167.1\|WP_168571930.1\|4112982_4115955_-\|type-I-secretion-system-permease/ATPase	gnl\|CDD\|225183	COG2274, SunT, ABC-type bacteriocin/lantibiotic exporters, contain an N-terminal double-glycine peptidase domain [Defense mechanisms].	0
NZ_CP051167.1\|WP_168570161.1\|4110990_4112787_-\|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	gnl\|CDD\|130902	TIGR01843, Hemolysin_secretion_protein_D_plasmid, type I secretion membrane fusion protein, HlyD family. Type I secretion is an ABC transport process that exports proteins, without cleavage of any signal sequence, from the cytosol to extracellular medium across both inner and outer membranes. The secretion signal is found in the C-terminus of the transported protein. This model represents the adaptor protein between the ATP-binding cassette (ABC) protein of the inner membrane and the outer membrane protein, and is called the membrane fusion protein. This model selects a subfamily closely related to HlyD; it is defined narrowly and excludes, for example, colicin V secretion protein CvaA and multidrug efflux proteins. [Protein fate, Protein and peptide secretion and trafficking].	3.05501e-27
NZ_CP051167.1\|WP_168570153.1\|4092510_4093131_+\|NADH-quinone-oxidoreductase-subunit-J	gnl\|CDD\|214335	CHL00016, ndhG, NADH dehydrogenase subunit 6.	3.21613e-60

>NZ_CP051167.1|WP_168570158.1|4097423_4105163_-|CHAT-domain-containing-protein
MNNSFRAIASLVLLSSLTGVSKSSFAQAIIPASDGTGTAVTPEGNHFNIHGGQPSADGANLFHSFEQFGLEAGQVANFLSNPEIENILGRITGGDASMINGLIQVSGGDSNLFLMNPAGILFGANASLNVPGDFFATSATGIGFSDNHWFDARGENAWANLVGTPSHFAFSSLQPGAIVNFGNLTLQPGHNLTLLGGSVLNAGTLSAPGGNITLAAVPGESAVRISQENQLLSLEVRPGTAEMGTFTPQSLPELLTGAGATHAKTVTVNPDGSLQLSGSGIAIDPQTGDTIISGEMTATGGQIAVLGDRVALIETKMNTSAPHGGGTVLVGGDLRGRGSVPNARQTFIDRHSSIAADATEFGDGGRVIVFARENAQIHGQLSALGGILGGDGGFVETSGLQSLEVSSVPNARTRCANVPTCGSGGEWLIDPNDIEIVAGAGTVNINNTTPFAATADSAQLGVDLIVAALTGGNQSVTIETGSGGTQEGKITVTAPIDFNGTGLNNTLTLNAHNNVYIYGQISDSVPGGDSLNLVLNGDIDNLGGGGIAIPYTTIHTGGGNFTATGTGSPTSRHGILLDNATINAEGGTITLTGRGLDGVDNNSGILLSNGSVLQTNGNGSIRLDGTGGSGVHWNTGLYTEWNTGLYIENATVTANGEILLTGTSGKGTNFNRGIFLDGAIVRSETGNIHLIGTGSNSSGEYNPGMVLQANSRLEAPQGTITLEGFGVNGTHWNGGIFVDESTLSADGDIRLTGIANGTGENNRGIGVTAGSLVESTTGSIVIDGTGGVQGFFNTGVAIRDGVSLSAYRDLRVTGMARGTEKVNDGISVMNGSTLQTEIGSIILEGTGGNGTSENYGIYIDNNVQISSNLGEINLTGTGGNGSEFANIGILFRGNSIIESKEGDIVLQGNGGTGDSLNHGIFANDNARIFSENGNISLTGIAREVTADLNQGVRLLNGSNITSQKGAIALEGQGGSGTDNNPGIFLTGSTISGHQSVILKGTGNGTGEGNLGIDLETGSTVEATGTEDLLLEGVGVSGAEGIGLNGVLINPTATGTGNLIFRGNNISFQGESRITTNNTLTLEPIAPGTAIAVNDATGDYSLTTEELLMLDVRSGNLTLGSDTVGNIYVGSLGEIDLSNSNYNLTLKTGQQIYVNNGIITDSQNLTLDGAVSLLRDVNFRTISGNITFNNTLDGAHHLTLNAGTGNIDFAGNIGSQTPLADLTIAQTHNLTTREINATNLTQLAGSGTTTFNGKITVTGATGIDLNTHTIHFNAPVTTTGLGGVTLANTENLNLVHPFNLNGPFTQIGTGTVTVASQIETNNNELRFNAPVTLMPGANLVPGTAILAFDSSLDIGNHPLTLTAGEIDFNGAVRGTNRLSLQPASPDRNIILGADTESDASFDLTANELSQFEDGFSAIALGRADFTGEITIVNSLQFSDPIALEAGSGSITANGSITGLGNGSIAFNAATIYLNSDLKTIDNNISLTGNIILGNEIEIDTNSAGGDIRILGNVDGNRDLTLNAGTGQIDLNGNLGETSPLEDLNITSNQTTIAGNMTTEGDTTFDGAIAIAGPVTITTHDGDLMIRGTLDSAIDSTENLTLNVGNGDLTFDRAVGSQQPLGQLKIDSATRITALEAIAAGSLSATSTDTIDLRGRVTTTGAAGVRLNAENALTVRDITSNGQPIALESRTANVQTGNLDSTSAPTGGAISVTSSQGEIITGNLTSTGVDRGGDITVMAKLAITSGAIDSSATVGDAGNVFLDPIGDIQVSSINAEGGTTGRGGDVFIETTGGFFRATDAFPSSYSPTGQASISTAGGAGGGSITLRHAGGDGLDPIEGFEIGNPAFHGTRDVVTTGTSTLNLGEIFPRSFTRGNITVSTDDGVDPVPEPQVVPEPEPVPEPQPVAEPEPVPEPQVVPEPEPVPEPEPLLEPEPQPVPEPEGVAETPQESLPAQTAPGAPPLEPISPQNGSPSEAVGGNNPLPEAIASEPNRTEAPEIAPLSPILPLAPSAIAPSSQVPVRSPIPASSEMAPNTIENNPLPQGNIESQMTAATNRTLPTAAPGSEFPSGQPTQSVGSVAILEPFSATSESIVPPKTIADGNINPASIPIDNSARSEPIVEVSMTGIELDTQITTLEEALSREFINHFNHPSHFNLLSLDEIRQVLRKTEEEMGMRTAVVYIVFGRTQLNDNAALVCPSGEHNQERDRDRFVRSDRILQEELGWPCDRHPEDPVELVVVTAFEKPLRLKIPEAHRQIVEQLAVEFRHKITDRKRSYSQLYLEPSQELYRLLIEPIQPTLEQRRIQNLIFVPDEGLRSLPFAALHDGEQFLVEQYSLAIVPSFSLTQPTYTNLKNEQVLAMGASEFEELTPLPAVPLELDAIVCGDRSRSSSCWSGKQFLNEEFTLNTLKEEVDSKEFSIVHLATHMDFQPGSADNSYIQLWDGRLRLSDMKDLQWQVAGVDLLVFSSCRSAIGDREAELGFAGLALQSGARSAIASLWYVSDNATLGLMSELYDNLRSAPIRAEALRQAQLEFIRGNVRLEAGQLMLSEGAIALPKQQDVREIKPLSHPYYWAGFTTIGNPW
>NZ_CP051167.1|WP_168570157.1|4096506_4097367_+|calcium-binding-protein
MRILLTIAHYFNPEGGGKHGSLGKNPQPRILALSQCIAHLWSVFGRSQSSIDIAQCAALPVNQAQANDLDIVICTTGDRHLLAQLPLDRNIYRHHATHAEPMFLGFECQAVLRDSLGHYDYYCYLEDDLILRDPWFFIKLKWFTQHAGDACLLQPNRYEIAMQGQRYKAYIDGDLAPKVTARFQNVKEAPELKGKIMEESVMFKRTLNPHSGCYFLNARQMAYWAQQPYFLDRDPSFIGPLESAATLGIMRTFKIYKPARDHAGFLEIQHFGSAFLQLIGNTVRLD
>NZ_CP051167.1|WP_168570156.1|4094749_4096405_+|glycosyltransferase
MPDSNLLGLIPADARRVVEICDDRPSNARESASQRATHYRRINPRGEYLTIACDRHASDVVEPAIVEQSVDCLVFDRTLTQVFDPLKLLQSSARWLSENGQVVACIPNVQYWHHLVYLLRGLGLEQGTNFDNCQLRFFSLETIKKLFNQAGLNLYEVQTVGVQTEAFKEFAHTLSPVVKELGLDPQTFATQANTESYLVRASKTESPPRRLFVHTILMAPTACDRPRVLDPDRLSNTIPGVRAIAEVKNADLSLALPQEEKVFIWQRTILKYPHDFARLRELLRRDYLIIAEIDDDPLRRPQYEQNRFLSYRGCHGVQTSTEPLADYLRQHNPNVAVFANQLTELPPERSYKNDGTCTIFFGALNREADWEPIVGELNRVLGKYRDRVRVKVIHDRKFWNALQSLEGDRKDFEAFCPYERYLEIMDECDLALLPLTPTRVNSMKSDLKFLECAGHGVAVLASPVVYEHTIVEGKTGLIYRTVEEFGKHLEALITDPLLRQTLAQNAYRWVAENRLLCQHYRQRSEWYKQLRDRLPELNRQLRDRLPELFAD
>NZ_CP051167.1|WP_168570155.1|4093707_4094628_+|NAD(+)-kinase
MQLKHAIIAHKAGDHLSRRRAEQCARELEARGCKVLMGPSGSKDNPYPVFLASATSAIDLALVLGGDGTALAAARHLAAENIPILAVNVGGHLGFLTQPSETFQDSEKVWDYLLEDRYAVQRRMMIEAQIFEGDRSNLIPASDRYLALNEMCVKPAAADRMITSILEMEIDGEVVDQYQGDGLLVATPTGSTCYTVSANGPIVHDGMEAMVVTPICPLSLSSRPIVLPPGSVVSIWPLADRDLSTKLWMDGVLASSIWPGHRVDVKVADCRAKFIILRENYSYYNTLREKLQWAGARIHYSNNHRN
>NZ_CP051167.1|WP_168570154.1|4093202_4093508_+|NADH-quinone-oxidoreductase-subunit-NuoK
MQLQYFLVLAAALFCIGIYGLITSRNAVRVLMSIELLLNAVNLNLMAFSNFLDSSEIKGQVFGVFVITVAAAEAAVGLAIVLAIYRNRDTVDMEQFNLLKW
>NZ_CP051167.1|WP_168570153.1|4092510_4093131_+|NADH-quinone-oxidoreductase-subunit-J
MNLAEGIQIISFGILSVALIGAALGVVLFSNIVYSAFLLGGVFISMAGMYLLLNADFVAAAQVLIYVGAVNVLILFAIMLVNKREDFVEMPNAWIRKGATALVSLGLFALLTTMVFSIPWEVSAVATQANGSIVTIGEHFFSDFLLPFELASVLLLMAMVGAIILARRDLLPDESSTPSEQRLMFEQLPERPREPVGSLQGSARDR
>NZ_CP051167.1|WP_168570152.1|4091810_4092434_+|NAD(P)H-quinone-oxidoreductase-subunit-I
MLNFLSKVGDYAKETLQAAKYIGQGLSVTFDHMSRRPITVQYPYEKLIPSERFRGRIHFEFDKCISCEVCVRVCPINLPVVDWEFNKETKKKNLKHYSIDFGVCIFCANCVEYCPTNCLSVTEEYELAAYDRHELNFDNVAMGRLPYKVTDDPMVSPMRELAYLPKGVVDPHVVPHTAPRAGKHPEDILQELEKQAERQTPEASSKN
>NZ_CP051167.1|WP_168570151.1|4090576_4091695_+|NADH-quinone-oxidoreductase-subunit-NuoH
MNPGIDLQGSFIQILTDLGIPAGLAKAIWMPLPMLLMLAVATVGVLVGVWLERKISAAAQQRIGPEYIGPLGILAPAADGLKLIFKEDIVPAQSDPILFTLGPILVVLPVFLSYLIVPFGQHLLITDLGIAIFLWIALSSIQPIGLLMAGYSSNNKYSLLGGLRAAAQSISYEIPLALSVLAIAMMSNSLSTVDIVQQQSSYGILGWNIWRQPAGFVIFWIAALAECERLPFDLPEAEEELVAGYQTEYSGMRFGLFYVGSYVNLMLSALLVSVLYLGGWEFPIPVETLAGWFGVSETAPWFQVLAGVLGIVMTLVKAYLFVFVAILLRWTVPRVRIDQLLDLGWKFLLPVALVNLLLTAALKLAFPVAFGG
>NZ_CP051167.1|WP_168570150.1|4089058_4090219_+|citrate-synthase
MTVAGDLKTTGFEFKPGLEGVPATLSSISYVDGKNGILEYRGIPIGELATQASFLETSYLLIWGELPTREELDAFEHEIRYHRRIKYRIRDMMKCFPESGHPMDALQASAAALGLFYSRRALDDPAYIRAAVVRLLAKIPTMVAAFQMMRKGNDPITPCDDLDYSANFLYMLTEREPDPLAAKVFDACLTLHAEHTINASTFSARVTASTLTDPYAVVASAVGTLAGPLHGGANEEVLEMLENIGSVDNVRAYVEHCIQTKSKIMGFGHRVYKVKDPRADILQNLAEQLFESTGRDDYYDIAIELERVVEEKLGHKGIYANVDFYSGLVYRKLGIPNDLFTPIFAIARVAGWLAHWKEQLAENRIYRPTQIYTGSHSAPFVAIAER
>NZ_CP051167.1|WP_168570149.1|4088388_4088895_+|phosphohistidine-phosphatase-SixA
MTPTEKRIYLIRHGIAADRADYERDADRPLTEEGFRKTRQIARRLEQLGLHFDRLLTSPLTRARQTAEILQEQGLSDTLEEYPHLKPAGNFQQWLHWYRDWQPSAETHLALVGHEPDLGHWAEQLVFGDIGDRLAIKKAGIVGLILPRTGSPVGKSVLFWLTPPKLLL
>NZ_CP051167.1|WP_168570159.1|4105739_4107704_-|calcium-binding-protein
MGPERGPDTVLGLNGSDILTSDTLNGGSIIFGNRDNDSLTGAGVGDTVYAGQDNDQIRSLGGSSLFFGDLGDDYFESVGTQGNDTVFGGDIDGTDEGNDIFNFGNGGGSNLGLGNKGDDFLSGSGFGEDSLYGGQGDDTVQVVELSSFGGTGIGFGGQDDFVPEATSLPNNRDLLPDVRPGGGGGAIGDDTVVVVDPDPISPAPLNPGRNYLVGDLGDDLVIGLGDRDSLWGHVGQDSLLMLGSIAGREDADPLDNSGTLNGVPQANWMDGGDGNDSLVAFGGLRGRQTLWGGEGDDTIKNYGVQGLVFGNEGNDSIDVTNFGLTLGRNTVYGGKGEDTIVSGGTNLVYGDKGSDTLISIGNNDTLYGDNDTAGTAAGNDFITAAGATSRLFGNEGNDSLITAGADATLDGGAGADSLSAAGENSWLTGQDGNDSLVASGSNSTLIGGDGNDSLFATEGTTGMSLLGGEGDDRLISNSNTDTLIGGAGNDVIVGSKEADTLRADGPGNDTLEGFLGADSLIGTRGSFDAFVYQSASTDELNDTITSFDTGIDKIHLDASDFFGGAGQATAGQPLRINLDFFPEQTQSGYSGTFTSSFTGADTPAIVFDAQDSGGILYYDPSGAAPAAGGAATSDLVTIAVIREGTVNANDIVLF
>NZ_CP051167.1|WP_168570160.1|4108731_4110945_+|tetratricopeptide-repeat-protein
MRINQTGVGVEIASDRAIADLERAEQFQRQENWDAAIACYRRALTHTGDPGEIYPHLAAVYLDAGQYPEAIATCQQALKRDPNRAELYHTLAIALDALDRPDAATRAYDRALDAWQQALQLPLRGTGGDRAFKLGNALLASGRLDAAICAYQRAIALQPQSAEAHSNLGIAWLQAGRGDRAVAALRRARALQPQSAGIAYNLAKALDAQLRRGDASADPHLSRQRFEALLDAVKLAPEFAEAHEMLLGTVISPQPQSASFSLLREIAAAYLRLCPPSWRSLALVGSVSVHLYSGTIPEAQAQLGELETEIYQNLGRLPDRFIRNLYSQVLFCLPHLRDDRGANSRLATFMGDRVRGVLDRQLQEPVATAKRANARPAPLKIGCLSAHFRRHSVGWCSRDVLRALSRICPDLYLYSSQAVAGDDLTREFQQFAAKFYQPSRRGEAVIAEIFDEMRRDRLDILIDLDSSTVSVHPEILYRRPAPICLSWLGFDAPYLDDRHYFLADWHTHPAGAERDYPEKLLRMPACFMAVGGFEARGFAESRPWGDRLVYLCVAPGKKLDRALVDAQIQILKQVPHSILLHKGQGDLEIIQEAYGEGCDRHRVERDRVQFLPQTETEEAHRAIYKTVDVLLDSYPYNGGTHNLEALYFELPVVTRVGEQFLSRMAYSFLKTLGIEAGISPTWEDYIDWGIKLGSDRELRAEIRQKLRRSRQPETLSPLWNPEKFARDLYEMLFKIAR
>NZ_CP051167.1|WP_168570161.1|4110990_4112787_-|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit
MTQDTFKPASPPVFDRPVILERSPIWASIIIWLILGMTTAGITWAAWAKVEQVIPTTGKLEPQGSVVDVKAPTGGVVRQIHVEGGQLVKKGDLLITFDPTAPEADVESLKELRESLMRENQFFTTALNGQTVGPVGSDLESLTRLRANLLSENQFLQAQVGGVATAGGGDDFDRNQEQLLAASRSEFNSRVAAASLQVQELREQLQQVEAQLPTAREQLRIARDQLERARDRVFQSQERVRKAEEQVRQSQDQIPTAREQLRTAEDSLQLNIEIRDRIQPLVEEGALSQLQFDRQQQEVLRGQAEVERLKAELLNRRNEVTAREAEVLNRENEVQQQRADVLSRENELEARKSEISRLENERDRLRVAIDRASQQRDNTAALSQKDILTKIAENQKRISEINAQLSRSKLENQKQIARIDGQLARAQQQLQYQELRAPVTGYVFDLEPNAEGYVATERDPNPLLKIVPDSQLEASVYIKNQDIALVLEALRKRKESGEKGVPVEINIEAFPATEFGKVEGILTSIGSDALAPTQERPYYAFPATIELNSQQFILQNNLQISLQSGMAVNANIRIGDRTVLQIFLNRLTRKTNSLETVK
>NZ_CP051167.1|WP_168571930.1|4112982_4115955_-|type-I-secretion-system-permease/ATPase
MMTSTVSPSEISAFLAQTPPFDRLGVDSLKALASKCQLLRYRTGQPIYERDKMPAQLVILYEGQARILGYDPYKQSLASLRLAQSGEVLGWTALVRGTACETVIASTETIAIVIPSHEFVHYIGNEPGFGEAFEQRASEIEIFELLALELQRQANATANLKDLTFKLLPDARIVNIPKGRSSKPAIDPNWLWIVSRGSVGEVEVGNRLNPDALGSKIQSDTGARLLGLPPFDLAASPTDRAGTLTPLDAEDTATIPYAPPKPPEPEPDPNAPPPKFPFVRGRGPINAPVACFEMLAKYFAIPFRRDPVKRVLENQIRTQGTLSLQSCGSVGAMIGLNGQMVSVPANLITRLKAPAMVRWQDSFAVLFAISPKQLTVAIPEKGIVRKKPEEFTEIWGAEGQVLLLQRGSTDRQENFNFWWFLPELLKYKGILVQVFIASFFVQLFGLANPLLTQVIIDKVIGQNSLDTLDVLGVLMVGVAFFEAALTGLRTYLFVDTTNRLDLSLGSQVIDHLLRLPLRYFDQRRVGELAGRVGELERIRQFLTGTALTVVLDAIFSVIYIAVMLSYSLLMTAVALATVPLFTLLIAIVSPIVQRLLRRRAERYADTQSYLVEVLGGIQTVKAQNIELKSRWNWYDRYARYISAGFKTVQTSTTASSISNFLNKLSGLFLLWVGAHLVLSNPPQMTLGQLIAFRIIASNVTGSLLRFVQVWQTFQETAMSVERLRDILEAKPEADESDRLNIPLPDIQGRVKFEDISFSFPGSQSLQLLNVNLEFEAGSFVGIVGLSGSGKSTLMKLLQRLYEPKGGRILIDGYDINKVELYSVRRQIGVVLQDTLLFNGTVRDNIALTNPDATDEQIVEAAKVAVAHDFIMDLANGYNTVVGEKGSALSGGQRQRIAIARTVLQNPRLLILDEATSALDYNSESQVSRNLAEAFAGRTVFFITHRLTTVKNADAIVMMDRGSVVEEGSHDELMALKGRYYALYQQQESQL
>NZ_CP051167.1|WP_168570162.1|4115948_4116704_-|peptidylprolyl-isomerase
MSDVLKVGNRSIKAQEIPALLKRYDLMPQFLRGIAIDEAIADFSCSDEERLRALEDLAVEHQLTSPEARQAWLDSQGLTEKEMEAMAVRKIAIEKFKTATWGPKVENYFMARKTFLDQVFYSLIRTKDFGVAQEVYFRIQENEQTFADAAREYSQGPEARTGGLLGPVPISQPHPLIGKLLSISQPGQLWPPRPLAEWFVIVRLEKFIPAKLDNDMRRRLIDEMFETWLREQVQNLNSSLQSLGLSAASQS
>NZ_CP051167.1|WP_168570163.1|4116967_4117153_+|hypothetical-protein
MQPTRLKQEKFRWSPGGKPVLECAFKKQTNISQLRHFFKRFSLKSGFWEREWAIASRELDV
>NZ_CP051167.1|WP_168570164.1|4117215_4119765_+|glycosyltransferase
MKVSIITPCYNGSAFIERALACVKQSTYQNIEHIIIDDRSTDGSFELLQQLQKDFDFTLLQSAVNQGPAQARNQAIAHATGKYILPLDCDNYFPEDYIEKLVTTAEDLGENYSPIYCEKIIYFGRLNREITVSDWSLKRLTLGPCMDMGSLFTRDAFTRAGGFDRHCQPMEDYGLFLSMALQGFEGFKVPHTKLFYNLRLDSVSDHFNLQGGIENKQKIIRYLVDKHQNQLQQLGFDPEAIAAKQMQSFGKNILKKWLDREQNKPTPSPSNSGDRAPATDEISETATTVQLNDPLFKFVPLDAKRIVEIGCDRGRSGKHYKQLNPHGEYIGIETDSERAIAATESLDRVIFGDLETLDPATVAIADNSVDCIIYNDRLSSLENPLNILKQHADWLNENGQVLARIPNVQYWRRILELLRGQPSGDRSNSVFFDDIRLFTIDKIQELFDKAGLHIYEVQNLNNDGENPDFQAFQKTIAPLLQKLAIDPATFASQSATETYLIRAQKSATPPRRLLVQTNMMGSWPVYRVRVLEPDAFTRTIPGVRILQTVKSAPLNVGLPHEEKVFIWQRSILRNPQDFPILRKLIELDYLIIAETDDDPLYRPEYENNQFLNFRGCHGVQTSTEPLGNYLRQHNPNVAVFPNQLAYLPPPRRYPEDETVRIFFGAFRREEDWQPLIASFNQVLAKYGDRVEVRVIYDRQFFEAIEVAKKQFKPMSSYEEYQAIMRSCDLAWLPLNPTRFNQMKSDLKFIECAGHGVTVLGSPTVYEASIADGETGLIYRDKQEFLEKLEAAIADRQLRQTIARNAYQWVATHRLQCLHYRQRHQWYLALRDRLPELNAQLRQRVPELFS
>NZ_CP051167.1|WP_168570165.1|4120000_4123870_-|response-regulator
MSIHRLQSLGVRLSQKFSLRTVFIVPFVVQILAAVGLTGYLSYRNGQEAVEDLATQLRDEIVNRIEQRLNSHLATPHTINQLNLDAVRLGELPLPETRNPENALRQLERHFWRQIQVFDSATYIYFGSPQEYFSGAERVGDGSFNVASWEARRGNEFYTYSTDEEGNRDRLVSAVPGYDLLTRPWYTTAVRAGKATWGEIYLWAAPYANLALPAVRPIYDRAGRLQGVFAVDISLLEIGQFLRTLEIGKTGQTFIIERDGQLVASSTPTPPFTTTGDRVERLQARHSSDRLVRATARFLDDRVPSLDRIEQPTQFRFDLDGEPQLVQVAPFHDERGLDWSIVVVIPESDFMARIHANTRTTIALCAVALVVAIAIGMATSRWVLGPIWRLNDAAKALADSHWEQSLPVNRADELGELARSFQRMAAQLQDSFAHLEAKNIQLQHLDQLKDEFLANTSHELRTPLNGTIGIAESMLDGATGTLTDLQRKNLITIAQTGRRLANLINDILDFSKLRHQNIELQLKPVGLREIVEVVLTLSQTLVGKKPLKLVNEIPEDLPAAWADENRLQQILYNLVGNAIKFTDTGAVTLSAWEVPDRQHLTVAVSDTGIGIPPDKLDRIFESFEQADGSTARQYGGTGLGLAITKQLVELHGGEIQVESTVGEGSRFAFTLPIAEDADPQIVSCQQRQSLSASVVSSLRDREAFDEIAPPEQDIPADPDGAIDSEKVKLLIVDDEPVNLQVLVNHLSLENYTIASASNGLEALEIIENGFEPDLVLLDVMMPKMTGYEVCQKLREHFPSTQLPILMLTAKNQVSDLVHGLGVGANDYLTKPISKNELLARIKTHLQIATISIENAKLYYELRESESRLKQFLEALPVGVVVLTGEGQPYYINRVGKDLLGRGVVSEVNSEGLGQVYQIYMARSDRLYPSEQLPMVRALRGERSTSDDLEIHRSDKRIPIEAWGTPIFDDKGDVTFAIVAFQDITERRQVEVERERFTEQLEQANLNLEEALEAELELTEAYGRFVPHEFLHFLGHETIVEVSLGDAIQKNMSILFSDIRDFTTISEQLTPEDSFKFINAYLSRMESAIADHDGFIDKYIGDAIMALFSGKADDAVKAAIAMLNRLKDYNQERLQLGETAVKIGIGINTGSIILGTVGGQNRMEGTAIGDAVNLAARIEGLTKNYGVSLLISHQTFLELEDANQYSLRLIDCVKVKGKSQTVSVFEVFDADPEDLKMSKLETKGTFESGVILYHLKSYSEAIVKFERCLQVDEGDRVARIYLERCRTQIL
>NZ_CP051167.1|WP_168570166.1|4123910_4127777_-|response-regulator
MIVNRIYMALAKLPKKVPIRTILIVPFILQIFAVVGLTGYLSFRNGQRSVEELVHQLSDKITDNIDRHLQNYLTTPHLLHRVTAASVRNGILDIEDFETVRRQFWSEIQLSDAVDYIYLGYKNGNFIGVQKYLDGRTVVKFRDESTEPNRDIYQLDDRGNIEEFLKSSPYDPRSRPWYETTLQERKQTWSEVYISADLGVLQVTPTTPIYDPDGNLVGVLGTNLILSQIGDFLQGLEISESGIAFIVEPGGETIASSTDESPFITPEEGEPKRLLAVESQNPLIRESSAYLLQHLPPLDRLDEPAHLTFSIDGKKQLLQVSPLDDDLGLKWAIVVVIPEADFMARIAANTRTTIGLCLLSLAIAILVGTRTARWIVKPIENLNHAAKKLASGEWEETPDCDRTDELGELACSFNKMARQLRDSFASLEAKNAQLQHLDKLKDEFLANTSHELRTPLNGTIGIAESMLDGATGVLSDLQRKNLLTIAQTGRRLATLINDILDFSKLRHKNIELQLKPIGLREIVEVVLSLSVPLIKRKHLQIINNIHDDLPPILADENRLQQIFHNLIGNAIKFTDAGVVEISATAISPETRPEIGEFGAIEITVSDTGIGIAEDKINRIFESFEQADGSTARQYGGTGLGLAVTKKLVELHGGKIRVESTFGEGSRFTFSLPIAEGEAVPLEGDRRSELSQLTTLSWSEDEVEIEALSSEQSLSPTPLDNQQKIKILIVDDEPVNLQVLSNYLSLENYAIVSASNGVEALTLIENGFEPDLVLLDLMMPKMTGYEVCQKLREHFPATELPILMLTAKNQVSDLVHGLGVGANDYLTKPISKNELLARIKTHLQIATISIENAKLYYELRESESRLKQFLEALPVGISILDSRGKPYYINRVGKELLGRGVVDASWEEVSEVYQNYIAGSDRLYPIERLPVIRALHGEQTTADDIEIQRGEKRIPIESWGTPIFDEKGEVSFAIVAFQDITERKQAEEERERFTQQLAAVNKDLEQSLEAQLELTDAYGRFVPHEFLDLLGQQSIVDVELGDSVEQEMSVLFSDIRDFTTISERLTPAENFKFLNSYLTRMEGAIADHHGFIDKYIGDAIMALFSSNADEAVQAGIAMLRLLQEYNQDPERSHNSPLNIGIGINTGNLMLGTVGGSNRMDGTAIGDAVNLASRIEGLTKNYGVQLLISHHTFLKLRHPTEYALRLLDRVQVKGKSKFVSVFEIFEADPPEMKEKKLVNKTVFEKAVLFYHFNWFYQAAQGFQQYLELNPGDRAAEIYLDRCEKHYGNLK
>NZ_CP051167.1|WP_168570167.1|4128144_4128693_+|dTDP-4-dehydrorhamnose-3,5-epimerase
MNVIPTAIPEVAILEPKIFGDDRGFFFESFNQRKFAEKTGFTGEFVQDNHSRSRKNVLRGLHYQIEQTQGKLLRVVLGSIFDVAVDIRKSSPTFGQWVGCVLSSENHRQFWIPAGFAHGFLVLSDVAEVLYKTTDYYAPQHERSLLWNDPDLAIDWPLHGETPILSEKDKAGKPLNAADLFA

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Crispr_ID: NZ_CP051167_19

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_19

4260425-4262673

TypeIII

N:A

Consensus_repeat	Method
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	PILER-CR
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CRISPRCasFinder
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CRT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	PILER-CR

30 spacers

cas1,cas2,csm3gr7,cas10

The CRISPR arrays of NZ_CP051167_19

>merge|NZ_CP051167|19|4260425-4262673|PILER-CR,CRISPRCasFinder,CRT,PILER-CR
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACCAGAGATCATTTGCAGGAAAAAAGATCTTTCCGTCGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACAAAGATTTTTCCGTATTTGCTTGGGTTGGAAACAACTCGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACGATTTAAAGTCTGTAAAAAGTGGGGGGAGCCGGTCCAGTGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACTTGAATTACAACATCAAGCTTTATCGCGGCGATGAAAGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACAACCGTGGAAAATCGCGAAGACCTTTTAACGATCTTTGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACAAATGGTCTTTCTGCTATTCAAGGCTTAGGTGGCACTCGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACGTTTTTCTTTTTGTTTTTTTCTTTTCTTTTTTCCTTCGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACTTGTTTCTTCTTCTTCTTTTTATCCCCACCCCTGGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACTATGTAGGCGGAATTCATTACGCTTTTTATGAGGGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACCTAGTTTGCGAGGAAGAGAGCGCAAAGATTCTAGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACCCGAACCTAGACAACACAAGAGTTTGACAGTCGGATTGCAGAAAGATACCGGATTTGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACGCGATACCGCACGATATGTGCGGTACCGTATCCAAGACAATAAGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACGTGGGGCGAACCCCTGGAACCGGGCTGGCCCCCGAACTGCGAACAGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACGTCTGCACTGAGTGGGAACTCCGTGACACAGACGGAGTGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACCCGTCGCAGCCTTAGATTTGATTATCCGGGGGACTCCCCCGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACGGGGTCCAAGTCGGCCCCTTCACAGGGCGAGGAGGGGGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACAAGTGGCTCGACTTTACGGTACACGGGTCCGCAAAATGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACTTTTTGTTAGGGCCCGGCATGTCCGGGAACCCGCAAGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACATTCCTAAAGAGGTTATCTGGTCCCAAATGGACCGCACCAGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACAGTTTCGAGCCAGCTGTCTGAGTTAGTTGGTCTTCCCAAAAAAGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACGTGGCTCCAGCTACGTATACGTAGGAGTGTACAATGTGCGGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACCCCTTGTCACTTTTGTCACTTGTTTTGTTTCTGCTTGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACGATCGTAATGGGGTGCAAAATGCACTCCAGGTAATCAGCTGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACTTTTCTTTTTTGTCCTTTCTGTTGCAGCCACTACTGCTGGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACAACCTGTTCTCGTACAGGTCGAAGTGTGTGTTAAGTGGGGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACGGGGTGTATAAGGGGGGGGGCTCCCCATACCTCCGTCTATTGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACAACTATACTACAAAGTATTTTTTACTCAAACTTGGGGAGAGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACTATCTCCGAGTATTCGGAAACAACAACATAGACTGTTGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACAAAAGTTTTATGTTTGGGGGGGCGACTACGTCTCCCTGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACTACGGCATGGCCGGACCCCACCCCTACGTGGGGGTATAGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC

>NZ_CP051167|19|14|4260425-4261103|PILER-CR
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CAGAGATCATTTGCAGGAAAAAAGATCTTTCCGTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAAGATTTTTCCGTATTTGCTTGGGTTGGAAACAACTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GATTTAAAGTCTGTAAAAAGTGGGGGGAGCCGGTCCAGT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTGAATTACAACATCAAGCTTTATCGCGGCGATGAAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AACCGTGGAAAATCGCGAAGACCTTTTAACGATCTTT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAATGGTCTTTCTGCTATTCAAGGCTTAGGTGGCACTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTTTTTCTTTTTGTTTTTTTCTTTTCTTTTTTCCTTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTGTTTCTTCTTCTTCTTTTTATCCCCACCCCTG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TATGTAGGCGGAATTCATTACGCTTTTTATGAGG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACCTAGTTTGCGAGGAAGAGAGCGCAAAGATTCTAGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACCCGAACCTAGACAACACAAGAGTTTGACAGTCGGATTGCAGAAAGATACCGGATTTGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GCGATACCGCACGATATGTGCGGTACCGTATCCAAGACAATAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTGGGGCGAACCCCTGGAACCGGGCTGGCCCCCGAACTGCGAACA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTCTGCACTGAGTGGGAACTCCGTGACACAGACGGAGT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CCGTCGCAGCCTTAGATTTGATTATCCGGGGGACTCCCCC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GGGGTCCAAGTCGGCCCCTTCACAGGGCGAGGAGGGG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAGTGGCTCGACTTTACGGTACACGGGTCCGCAAAAT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTTTTGTTAGGGCCCGGCATGTCCGGGAACCCGCAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	ATTCCTAAAGAGGTTATCTGGTCCCAAATGGACCGCACCA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AGTTTCGAGCCAGCTGTCTGAGTTAGTTGGTCTTCCCAAAAAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTGGCTCCAGCTACGTATACGTAGGAGTGTACAATGTGCG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CCCTTGTCACTTTTGTCACTTGTTTTGTTTCTGCTT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GATCGTAATGGGGTGCAAAATGCACTCCAGGTAATCAGCT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTTTCTTTTTTGTCCTTTCTGTTGCAGCCACTACTGCTG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AACCTGTTCTCGTACAGGTCGAAGTGTGTGTTAAGTGGG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GGGGTGTATAAGGGGGGGGGCTCCCCATACCTCCGTCTATT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AACTATACTACAAAGTATTTTTTACTCAAACTTGGGGAGA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TATCTCCGAGTATTCGGAAACAACAACATAGACTGTT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAAAGTTTTATGTTTGGGGGGGCGACTACGTCTCCCT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TACGGCATGGCCGGACCCCACCCCTACGTGGGGGTATA


>NZ_CP051167|19|17|4260425-4262673|CRISPRCasFinder
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CAGAGATCATTTGCAGGAAAAAAGATCTTTCCGTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAAGATTTTTCCGTATTTGCTTGGGTTGGAAACAACTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GATTTAAAGTCTGTAAAAAGTGGGGGGAGCCGGTCCAGT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTGAATTACAACATCAAGCTTTATCGCGGCGATGAAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AACCGTGGAAAATCGCGAAGACCTTTTAACGATCTTT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAATGGTCTTTCTGCTATTCAAGGCTTAGGTGGCACTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTTTTTCTTTTTGTTTTTTTCTTTTCTTTTTTCCTTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTGTTTCTTCTTCTTCTTTTTATCCCCACCCCTG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TATGTAGGCGGAATTCATTACGCTTTTTATGAGG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CTAGTTTGCGAGGAAGAGAGCGCAAAGATTCTA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CCGAACCTAGACAACACAAGAGTTTGACAGTCGGATTGCAGAAAGATACCGGATTT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GCGATACCGCACGATATGTGCGGTACCGTATCCAAGACAATAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTGGGGCGAACCCCTGGAACCGGGCTGGCCCCCGAACTGCGAACA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTCTGCACTGAGTGGGAACTCCGTGACACAGACGGAGT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CCGTCGCAGCCTTAGATTTGATTATCCGGGGGACTCCCCC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GGGGTCCAAGTCGGCCCCTTCACAGGGCGAGGAGGGG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAGTGGCTCGACTTTACGGTACACGGGTCCGCAAAAT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTTTTGTTAGGGCCCGGCATGTCCGGGAACCCGCAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	ATTCCTAAAGAGGTTATCTGGTCCCAAATGGACCGCACCA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AGTTTCGAGCCAGCTGTCTGAGTTAGTTGGTCTTCCCAAAAAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTGGCTCCAGCTACGTATACGTAGGAGTGTACAATGTGCG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CCCTTGTCACTTTTGTCACTTGTTTTGTTTCTGCTT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GATCGTAATGGGGTGCAAAATGCACTCCAGGTAATCAGCT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTTTCTTTTTTGTCCTTTCTGTTGCAGCCACTACTGCTG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AACCTGTTCTCGTACAGGTCGAAGTGTGTGTTAAGTGGG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GGGGTGTATAAGGGGGGGGGCTCCCCATACCTCCGTCTATT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AACTATACTACAAAGTATTTTTTACTCAAACTTGGGGAGA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TATCTCCGAGTATTCGGAAACAACAACATAGACTGTT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAAAGTTTTATGTTTGGGGGGGCGACTACGTCTCCCT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TACGGCATGGCCGGACCCCACCCCTACGTGGGGGTATA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC

>NZ_CP051167|19|8|4260425-4262673|CRT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CAGAGATCATTTGCAGGAAAAAAGATCTTTCCGTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAAGATTTTTCCGTATTTGCTTGGGTTGGAAACAACTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GATTTAAAGTCTGTAAAAAGTGGGGGGAGCCGGTCCAGT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTGAATTACAACATCAAGCTTTATCGCGGCGATGAAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AACCGTGGAAAATCGCGAAGACCTTTTAACGATCTTT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAATGGTCTTTCTGCTATTCAAGGCTTAGGTGGCACTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTTTTTCTTTTTGTTTTTTTCTTTTCTTTTTTCCTTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTGTTTCTTCTTCTTCTTTTTATCCCCACCCCTG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TATGTAGGCGGAATTCATTACGCTTTTTATGAGG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CTAGTTTGCGAGGAAGAGAGCGCAAAGATTCTA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CCGAACCTAGACAACACAAGAGTTTGACAGTCGGATTGCAGAAAGATACCGGATTT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GCGATACCGCACGATATGTGCGGTACCGTATCCAAGACAATAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTGGGGCGAACCCCTGGAACCGGGCTGGCCCCCGAACTGCGAACA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTCTGCACTGAGTGGGAACTCCGTGACACAGACGGAGT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CCGTCGCAGCCTTAGATTTGATTATCCGGGGGACTCCCCC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GGGGTCCAAGTCGGCCCCTTCACAGGGCGAGGAGGGG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAGTGGCTCGACTTTACGGTACACGGGTCCGCAAAAT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTTTTGTTAGGGCCCGGCATGTCCGGGAACCCGCAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	ATTCCTAAAGAGGTTATCTGGTCCCAAATGGACCGCACCA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AGTTTCGAGCCAGCTGTCTGAGTTAGTTGGTCTTCCCAAAAAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTGGCTCCAGCTACGTATACGTAGGAGTGTACAATGTGCG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CCCTTGTCACTTTTGTCACTTGTTTTGTTTCTGCTT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GATCGTAATGGGGTGCAAAATGCACTCCAGGTAATCAGCT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTTTCTTTTTTGTCCTTTCTGTTGCAGCCACTACTGCTG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AACCTGTTCTCGTACAGGTCGAAGTGTGTGTTAAGTGGG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GGGGTGTATAAGGGGGGGGGCTCCCCATACCTCCGTCTATT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AACTATACTACAAAGTATTTTTTACTCAAACTTGGGGAGA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TATCTCCGAGTATTCGGAAACAACAACATAGACTGTT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAAAGTTTTATGTTTGGGGGGGCGACTACGTCTCCCT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TACGGCATGGCCGGACCCCACCCCTACGTGGGGGTATA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC

>NZ_CP051167|19|15|4261228-4262673|PILER-CR
	CAGAGATCATTTGCAGGAAAAAAGATCTTTCCGTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAAGATTTTTCCGTATTTGCTTGGGTTGGAAACAACTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GATTTAAAGTCTGTAAAAAGTGGGGGGAGCCGGTCCAGT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTGAATTACAACATCAAGCTTTATCGCGGCGATGAAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AACCGTGGAAAATCGCGAAGACCTTTTAACGATCTTT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAATGGTCTTTCTGCTATTCAAGGCTTAGGTGGCACTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTTTTTCTTTTTGTTTTTTTCTTTTCTTTTTTCCTTC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTGTTTCTTCTTCTTCTTTTTATCCCCACCCCTG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TATGTAGGCGGAATTCATTACGCTTTTTATGAGG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACCTAGTTTGCGAGGAAGAGAGCGCAAAGATTCTAGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAACCCGAACCTAGACAACACAAGAGTTTGACAGTCGGATTGCAGAAAGATACCGGATTTGTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GCGATACCGCACGATATGTGCGGTACCGTATCCAAGACAATAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTGGGGCGAACCCCTGGAACCGGGCTGGCCCCCGAACTGCGAACA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTCTGCACTGAGTGGGAACTCCGTGACACAGACGGAGT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CCGTCGCAGCCTTAGATTTGATTATCCGGGGGACTCCCCC
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GGGGTCCAAGTCGGCCCCTTCACAGGGCGAGGAGGGG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAGTGGCTCGACTTTACGGTACACGGGTCCGCAAAAT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTTTTGTTAGGGCCCGGCATGTCCGGGAACCCGCAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	ATTCCTAAAGAGGTTATCTGGTCCCAAATGGACCGCACCA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AGTTTCGAGCCAGCTGTCTGAGTTAGTTGGTCTTCCCAAAAAA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GTGGCTCCAGCTACGTATACGTAGGAGTGTACAATGTGCG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	CCCTTGTCACTTTTGTCACTTGTTTTGTTTCTGCTT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GATCGTAATGGGGTGCAAAATGCACTCCAGGTAATCAGCT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TTTTCTTTTTTGTCCTTTCTGTTGCAGCCACTACTGCTG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AACCTGTTCTCGTACAGGTCGAAGTGTGTGTTAAGTGGG
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	GGGGTGTATAAGGGGGGGGGCTCCCCATACCTCCGTCTATT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AACTATACTACAAAGTATTTTTTACTCAAACTTGGGGAGA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TATCTCCGAGTATTCGGAAACAACAACATAGACTGTT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	AAAAGTTTTATGTTTGGGGGGGCGACTACGTCTCCCT
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC	TACGGCATGGCCGGACCCCACCCCTACGTGGGGGTATA
GTTTCAGCACCTTTTCCCTTCAAAGAGGGTCAAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168571943.1\|4279251_4281507_-\|hypothetical-protein	cas10	cd09679_cas10_CAS-III	gnl\|CDD\|187810
NZ_CP051167.1\|WP_168570250.1\|4256313_4258047_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP051167.1\|WP_168570246.1\|4245137_4247498_-\|DUF4131-domain-containing-protein	unknown	unknown	gnl\|CDD\|377126
NZ_CP051167.1\|WP_168570252.1\|4258775_4259138_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570247.1\|4247550_4248024_-\|DUF4079-domain-containing-protein	unknown	unknown	gnl\|CDD\|372553
NZ_CP051167.1\|WP_168570251.1\|4258171_4258723_-\|periplasmic-heavy-metal-sensor	unknown	unknown	gnl\|CDD\|197366
NZ_CP051167.1\|WP_168570248.1\|4248100_4249000_-\|glycine--tRNA-ligase-subunit-alpha	unknown	unknown	gnl\|CDD\|236473
NZ_CP051167.1\|WP_168570254.1\|4262905_4266508_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227922
NZ_CP051167.1\|WP_168570249.1\|4254747_4256214_-\|two-component-sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|223715
NZ_CP051167.1\|WP_168570256.1\|4271487_4272495_+\|CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|272998
NZ_CP051167.1\|WP_168570244.1\|4244032_4244215_-\|replication-restart-DNA-helicase-PriA	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570255.1\|4266670_4268677_+\|CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|376633
NZ_CP051167.1\|WP_168570258.1\|4273153_4274671_+\|hypothetical-protein	csm3gr7	pfam03787_csm3gr7_CAS-III-A:CAS-III-D	gnl\|CDD\|377130
NZ_CP051167.1\|WP_168570262.1\|4278211_4279255_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570253.1\|4259134_4259701_-\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|237124
NZ_CP051167.1\|WP_168570257.1\|4272558_4272837_+\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP051167.1\|WP_168570260.1\|4276891_4277326_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570245.1\|4244578_4244812_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570261.1\|4277421_4278240_-\|CRISPR-associated-protein	csm3gr7	pfam03787_csm3gr7_CAS-III-A:CAS-III-D	gnl\|CDD\|224255
NZ_CP051167.1\|WP_168570259.1\|4276312_4276627_+\|nucleotidyltransferase-family-protein	unknown	unknown	gnl\|CDD\|224583

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168571943.1\|4279251_4281507_-\|hypothetical-protein	gnl\|CDD\|187810	cd09679, Cas10_III, CRISPR/Cas system-associated protein Cas10. 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; Multidomain protein with permuted HD nuclease domain, palm domain and Zn-ribbon; MTH326-like has inactivated polymerase catalytic domain; alr1562 and slr7011 - predicted only on the basis of size, presence of HD domain, and location with RAMPs in one operon; signature gene for type III; also known as Crm2 family.	2.46638e-12
NZ_CP051167.1\|WP_168570250.1\|4256313_4258047_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	1.14626e-176
NZ_CP051167.1\|WP_168570246.1\|4245137_4247498_-\|DUF4131-domain-containing-protein	gnl\|CDD\|377126	pfam03772, Competence, Competence protein. Members of this family are integral membrane proteins with 6 predicted transmembrane helices. Some members of this family have been shown to be essential for bacterial competence in uptake of extracellular DNA. These proteins may transport DNA across the cell membrane. These proteins contain a highly conserved motif in the amino terminal transmembrane region that has two histidines that may form a metal binding site.	1.09244e-51
NZ_CP051167.1\|WP_168570247.1\|4247550_4248024_-\|DUF4079-domain-containing-protein	gnl\|CDD\|372553	pfam13301, DUF4079, Protein of unknown function (DUF4079). This is an uncharacterized family of proteins.	5.56196e-36
NZ_CP051167.1\|WP_168570251.1\|4258171_4258723_-\|periplasmic-heavy-metal-sensor	gnl\|CDD\|197366	cd09916, CpxP_like, CpxP component of the bacterial Cpx-two-component system and related proteins. This family summarizes bacterial proteins related to CpxP, a periplasmic protein that forms part of a two-component system which acts as a global modulator of cell-envelope stress in gram-negative bacteria. CpxP aids in combating extracytoplasmic protein-mediated toxicity, and may also be involved in the response to alkaline pH. Functioning as a dimer, it inhibits activation of the kinase CpxA, but also plays a vital role in the quality control system of P pili. It has been suggested that CpxP directly interacts with CpxA via its concave polar surface. Another member of this family, Spy, is also a periplasmic protein that may be involved in the response to stress. The homology between CpxP and Spy suggests similar functions. A characteristic 5-residue sequence motif LTXXQ is found repeated twice in many members of this family.	2.99821e-17
NZ_CP051167.1\|WP_168570254.1\|4262905_4266508_-\|hypothetical-protein	gnl\|CDD\|227922	COG5635, COG5635, Predicted NTPase (NACHT family) [Signal transduction mechanisms].	1.91443e-13
NZ_CP051167.1\|WP_168570249.1\|4254747_4256214_-\|two-component-sensor-histidine-kinase	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	9.52298e-60
NZ_CP051167.1\|WP_168570256.1\|4271487_4272495_+\|CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|272998	TIGR00287, CRISPR-associated_endonuclease_Cas1, CRISPR-associated endonuclease Cas1. This model identifies CRISPR-associated protein Cas1, the most universal CRISPR system protein. CRISPR is an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, a system for heritable host defense by prokaryotic cells against phage and other foreign DNA. Cas1 is a metal-dependent DNA-specific endonuclease.	5.07645e-23
NZ_CP051167.1\|WP_168570248.1\|4248100_4249000_-\|glycine--tRNA-ligase-subunit-alpha	gnl\|CDD\|236473	PRK09348, glyQ, glycyl-tRNA synthetase subunit alpha; Validated.	0
NZ_CP051167.1\|WP_168570255.1\|4266670_4268677_+\|CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|376633	pfam01867, Cas_Cas1, CRISPR associated protein Cas1. Clustered regularly interspaced short palindromic repeats (CRISPRs) are a family of DNA direct repeats found in many prokaryotic genomes. This family of proteins corresponds to Cas1, a CRISPR-associated protein. Cas1 may be involved in linking DNA segments to CRISPR.	1.08231e-113
NZ_CP051167.1\|WP_168570258.1\|4273153_4274671_+\|hypothetical-protein	gnl\|CDD\|377130	pfam03787, RAMPs, RAMP superfamily. The molecular function of these proteins is not yet known. However, they have been identified and called the RAMP (Repair Associated Mysterious Proteins) superfamily. The members of this family have no known function they are around 300 amino acids in length and have several conserved motifs.	3.72196e-09
NZ_CP051167.1\|WP_168570253.1\|4259134_4259701_-\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|237124	PRK12518, PRK12518, RNA polymerase sigma factor; Provisional.	1.03093e-89
NZ_CP051167.1\|WP_168570257.1\|4272558_4272837_+\|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.	4.72875e-25
NZ_CP051167.1\|WP_168570261.1\|4277421_4278240_-\|CRISPR-associated-protein	gnl\|CDD\|224255	COG1336, COG1336, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	1.98867e-18
NZ_CP051167.1\|WP_168570259.1\|4276312_4276627_+\|nucleotidyltransferase-family-protein	gnl\|CDD\|224583	COG1669, COG1669, Predicted nucleotidyltransferases [General function prediction only].	8.35941e-26

>NZ_CP051167.1|WP_168570253.1|4259134_4259701_-|sigma-70-family-RNA-polymerase-sigma-factor
MPTEATETDAELVTRCQEGDRASFRQLYRRYHGKVRSTLYPLCGLSNIDDLVQEVFLRAWKGLPKLKQPAHFGTWLYRISWNVASDRRQAYAKQHQKQERLIGTLPDRDRAGSPETDLMTLHYQDLVKRGLSHLSFDHRSVLVLHDLEDVPQKAIAEILQIPVGTVKSRLFHARSAMRKFLEGEGVQL
>NZ_CP051167.1|WP_168570252.1|4258775_4259138_-|hypothetical-protein
MNQPNDPDRRLVQFLREYAPDVPPPSPELEDRTIDALDGPHPIAVNRAKLRQLRPLWLVPVGIAAGLVVVWNGTRSPIPPQPSAEELAQLETYMETTWDGVLGETSLTESSDWFFPEASE
>NZ_CP051167.1|WP_168570251.1|4258171_4258723_-|periplasmic-heavy-metal-sensor
MKGRMHRRQLCALTALSVLLGTTAAYAAPPEFGNPEIVAQRPGGPGRGRGQGGQRWIEQLDLSQDQQQRIQQIRDRYRSEAESTYTQMMQLRQEMQDLMVGNGSDSQLRSKHDEMMKLHQRMGELRFDQMLEIRAVLSAEQRQQWAQQMQQRHQNRGNRQGNRPGNGRGMGPGGGMDDDFFGE
>NZ_CP051167.1|WP_168570250.1|4256313_4258047_-|ABC-transporter-ATP-binding-protein
MIRSSYGLLLPYLKPQWKTIAQALACTLGFTAFWPILARLAGDMAASIGAGDVATIAQLAGSAAVVFLVRGAVQYGQDALMAKAALAIALDLRQRVYAHLLHLSLGYFSHTQTGDLSYRLTEDIDRIGEVINKIFHQFVPCILQLIVVFSYMIYLNWQLTLASSIVAPLMALSIAWFGEKLRVFSHNSQSRIADLSAIVTEVFGGIRLVQAFCAEDYTLDRFRQAAERNRQARFSAEQLKAIQFPVVGFLEALSVLLLFFLGGWQIAQNNLTGSEFVSYVAAVALSIDPIAITTSNYNEFKQGEASVERVFELLSRQPEVTDKPGAIALPPVKGRIEYRDVTFSYHGKGPYPRPVLQEIDLTVSPGEAIALVGPSGAGKSTLVNLLPRFYDVQSGQVAIDGIDVKSVTLASLRRQIAIVPQETKLFTGTIAENIAFGQLDYDLDRVEAAAKIANAHEFITQMSEGYRSWVGEGGVNLSGGQRQRIAIARAVLLDPTILILDEATSALDSESEGAIQEALDRLMQGRTVLIIAHRLTTVRRCDRIVVLENGQILESGTHGELLAQEGRYAQFHAQQFY
>NZ_CP051167.1|WP_168570249.1|4254747_4256214_-|two-component-sensor-histidine-kinase
MTLIRRWIARPVHWLPKFDPHSLQIRLTVGMALVSALGIGTLAIATSWQMQRQLVATHKQTIKYIFDRFDRDVMHYSERNPAEKGLQPAIDSLSADRVLLWVKRPDGAIAAQSMPLSGRDDDTSKGLLGLPARQMMPQVSEIGGRFWVWCSGPLTVKGTHLGQLYIAADITEDRGILEGLIRTLALASGAAIVAMTVAIALYVRRSLRPVLEIGQLADRISVRELDTARIQLQNAPSEVRQLAQTCNTMLDRLAQSWEQQRQFVSNVSHELRTPLTLVSGYLQSTLRRATNLSEPQREALEIAASEAERTIQLLQDLLDLARADRGYLHFQLEPLLIVDLVAEVVEMAKQYSHREIAIVCGEDLLEASADRNRLKQVLLNLIDNAVKYSPSDTEIKVGVRSFGDRAIVEICDRGVGIPLAQQGRIFERFYRVDEARSRSVSPGESLATGGTGLGLSIVKTLVEGMGGTVTVRSKPGEGSTFGVILQRD
>NZ_CP051167.1|WP_168570248.1|4248100_4249000_-|glycine--tRNA-ligase-subunit-alpha
MNFQSLVATLNQFWSDRGCLIAQPYDMEKGAGTMNPHTFLRAIGPEPWSVAYIEPCRRPTDGRYGENPNRYQHYYQYQVLLKPSPNNIQEIYLDSLRALGIAPEDHDIRFVEDNWEAPTVAAWGVGWEVWLDGMEITQFTYFQQCGGIDCRPVSIEITYGLERLAMYLQNIDAMAKIAWTDDIRYGDVHLQGEIEQCTYNFEASNPELLFTLFGLYEQEAQQLVDRGLVLPTLDYVLKCSHTFNLLDARGVIAVTERTRYIGRIRHLARRVAQLYLEQREALGFPLLNSSTPTETASAA
>NZ_CP051167.1|WP_168570247.1|4247550_4248024_-|DUF4079-domain-containing-protein
MDLTQILEPIASQFRNLGIPEPIVHWGHPLMMGIVVFVMGSYVGWSGWRARVVGAGETAVQSRSDHRKLAPWMFLFMALGYTGGLLSLVMQREPILESPHFWTGSIALILLGINSILSLNFGDDRPNLRTAHAYLGSIVLGLIVLHALLGLKLGLSL
>NZ_CP051167.1|WP_168570246.1|4245137_4247498_-|DUF4131-domain-containing-protein
MTAAPLILLCLAYIAGLLASAIPGGRYGLLVLGIGAGIGVFLKLPGYLRCLKAGLKPAFFIAAGALALIAAFYLQLRLPQPQTDDISHYIAPTTGIGEQPAVTVLGKVTSTPRLTRSNKVQFWFDVTQLNELVGSADPIATVPPTSRTQPVSGKLYVTVPLLQGTGVHPGRRLSISGELYKPEPPKNPGAFDFQAYLASRGSFAGLRGEQVYFLSETREEGWGLWRVQRRIVRSQVRWLGVPHGPLVSAIVLGRRVVDLSIEVRDRFIQVGLAHVLAASGFHVALILSLVRLLTRPLSERLQFGAGSAVLMLYVILTGGSASVSRAAIMGFAALLAPLLQKQVKPLGSLLLAATILLLLQPGWIWDLGFQLSFLATLGLLVTVPSIVERLDWLPVTIASALAVPIAATIWTLPLQLYVFHVVSPYSIAVNLITTPLVSAITIGGFISAIAGAIWPLAGSALAWLLYYPVEGLLEIVEFFANLPGNSVATGALSIAQVVLLYTTIAAIWVIPWLQRQRRWGLGVLFAIALVVTPTLHAKATVVQMTVLATPRDPVLVIQNRGQVALVNSGDDRTTQFTILPFFRQQAIARLDWAISTAPVSSNTGWHQLFDRLDIALFSAPEPSPEEGDLLSHEAILHDLEQFEGSYEPLREDETLKFGAIAVRPISFEPMVVELQFDGQTWLWLGNLDPSQQNRWLGAGILPGSRPESSLDVLWWSGDQVTPYLLDALQPEVAIAASEEIDPATATLLEQKNIRIYITGLEGAVRWTPTQGFESHGAIAEDRIPWI
>NZ_CP051167.1|WP_168570245.1|4244578_4244812_+|hypothetical-protein
MISIAFLGNFPFLLGASLGRDRDRLEGFMLTSIAARIDTSATQVSRGNARDRLIEINRICSDFVFLDFFRFYRYFVN
>NZ_CP051167.1|WP_168570244.1|4244032_4244215_-|replication-restart-DNA-helicase-PriA
MQTIQAIRCPNCGNHAERYHFVHLKQTQTQCPVCDYFMVTCSRTGRVVEAYAPGTYATQV
>NZ_CP051167.1|WP_168570254.1|4262905_4266508_-|hypothetical-protein
MSARSLIASHEGIVKAERALKRLNLTRTAIAKEHQIASWSTVSKFFNYKPVDRSFFQEICHLLDLDWQDIAASPDDSQLDDSNADMTDSEKAAQCDRALLDAVIRNGDRTRKALEPYILPTIRRETFLEKCLQQIELGLSGKPRIVPILGAAGYGKSTILGTLYDELTGDREAAWVALVRCDDLLESALSFPEEVGEKASDRRVTIADLAAQLTVEHGRGVLLLDTLDIVLTKTLVPILRALFAELLEWETTVVFTCRHNDYADFFEPYHESFAGFREQVYDGCKLTPFALEEVTLAARLFARLKTEFPTEESQITFADRLLALCADRVSLTEIVCNPLLLALLCELFAEAQVVPEDLTVSQLYEIYWNWKIAKVRHQQQSRRIGKAKEKLCLFLAERLYCHSGERLRDFLYETSLDLTDETDFIAYTALRSDGIVKELGNDRIGFFHQTFLEYAIARWWNGTESGETAQFVIRQELQSPSGQVRHYIWPIFRQFFTLLPLNQFEQISNELDRTQLLPFRAISLAAVSRIEPEATRVLFPLLELAQLRQGAFIETLLIALNSAPQRHDSTVWDLLVKLLSTVGQDALNKTLEIAAVAIARHPEAGARFPEALTALMSHPEIEGDREQGYRFLGKFLNEYYREIRLRDRAIERPVLTALKEYYASLGSKVRSLAIDLYLSEGVPSAVKADFLLTILQLPPANNSFFEREKAIALTVELLPDLLATQSTILGESWLTAFEAPLPTESLGVIAAAVGQHAIDNRQWMAEMVTYLLIDPPSRLSKSFNSNCTIALKEIVQAGGGDRLVKYFLSLEVEQILDNRISTLSTILKTLAQVEGDRLTIDEVLAVQLAQWLRPRLISHPVESIRILDGLAVQFPGVKPILTQGLREIFARTKTRQVNQILKKLHCLPAELAPDLEARQNSKEARIALLKLLRDRAQRGDRESLERTIAFCGDRSQDLAKAASWTVLDLGWENIGIAIESLLPILRDSPIVVVRQNCLKVILEGVNDFGITPTEIAKVLEVMAEEKSPEVLQGMYQLCTAAIWHHPSGERRVEQAIAKAIFKLTRSVLVQAPQMTVDMMANSAWIAFNQMAFLEERSLIPDLLECTHLLWRAIDVRGKIDKTMVTGLLNQLGKYDPQFLEGLVLEAIGEEGNSLPLANWQALVVAIAHNQGKFSPLLDRVIDDPHIPLEVKHRIYQIRDL
>NZ_CP051167.1|WP_168570255.1|4266670_4268677_+|CRISPR-associated-endonuclease-Cas1
MNFTREQLKAAWQQVRRRSRQAGIDGMTVDRFARDLDEYLSQIQHHLNAETYRALPAKGFYLPKANGGKRSIGIPTVRDRIVQRVLLEELYWPLEETFLDCSYAYRPGRSIHGAARHFSTYTQFQPCWVLKADIAQFFDRLCRSLLLTQLEQLDLEPILVQLLEQQISAGIVIRGQYQNFGQGVLQGAILSGALANLYLTDFDRRSLAAGLNLVRYGDDFAIATSSRRQAQQVLECVGEWLAQVYLTLNPNKTHIYSPDDEFTFLGYRFLGHQFYPPPPPKRPETGEWLLSPSGVPYRRLKPRRTPRVSRPPRGSDSSPMGLPMAHSEHLWSERMTSLYITDQGAYLRVKNQQFEVFYDRQLRVKVPASRVSYIVLFGCCNMSHGAVSLALRRRIPVMFLSQKGRYFGRLYSESHAKVDYLTRQVQCALDSEFTRLQAEAIVAAKLHNSRALLLKLNRRRPTDAAFIALEMLASCRDKLSLAESMDALRGYEGKAASAYFQGLGSLFADPFTFSKRTKRPPTDPINSMMSLGYTLLSQNVHSFVNLAGLHPHFGNLHVPRDNHPALVSDLMEEFRAQIVDSLVAYLVNSKILTPDDFTLPDERNGVYLQPHALKKYLKHWEDKLLSEITHPHTQYKVSLKRCIELQVREYLACLTGEVEVYRPMLWKV
>NZ_CP051167.1|WP_168570256.1|4271487_4272495_+|CRISPR-associated-endonuclease-Cas1
MTAIYLTQPGSLLDAKRGVFELWHDDRRQRRIPAKLTSQILVFEDSQLSKTAIALAISFRLPVLFLDRHHRHLGRLHLNPNSGSQHRSRPGTPDPDDRRDLAERLVSAILNSRQSLLNTLDGAICPTVELTRGTIARILDELPTASGDRLREHLTGVDRLYYPALRQWLRLSAGTVLAPIDPWFYLAHSLLEQVTYGFVLDAGVNPYESILHCDTGDNLPLVRDLMLEWTVTLVDLLVLRFCMDEFLFSGNGNGSHSPLSRLRDRFVQQWETQLASEAIAGTSYRQCLFAQVRRYREALWGDRLYSPVLLRSESFVSGQPLRALRSRRSPCTHLT
>NZ_CP051167.1|WP_168570257.1|4272558_4272837_+|CRISPR-associated-endonuclease-Cas2
MLYLVCYDITKDSRRVRVAKLLETYGMRVQQSVFELVLNEQQYATLEKRLVKLLDRREDQLRFYPLPPQVRDRVTILGVRSPFAIDDPTIIV
>NZ_CP051167.1|WP_168570258.1|4273153_4274671_+|hypothetical-protein
MNLPLPTSLPRWYTVKENEEKGWTPETDDIVDKPENREITQAWNGSFCPPEASQFTLRLNNLQVISPVQVGGGSFREGHILPAQFGGIPCIPGSSIRGALLKWMRRIWSDLPPDEQAFWNKLIEGDRSGWQPRQIRFESLFLKKHLKPFPLYAQQSWQVFDTRSNQLGVQWQVSPVLPPTSPPKFSIQVLLSQEATESEKSWLRNRLEEMLKEQGLGRGTASGFGRMARSLPLTATWEIALTGTKPAIQQQDNKENIVGKYRWSPQVLRATLRGYFTRVALSLLSRNDAETLTSKIFGGLNSPARLTLTSYLTQCQRSPTAGTNYANIPAKDAHSTWIIRADCTPEFQDLIDPLLNIASRIGGLGPGWRRPPHSFRNNSLFRGSEFTLTPKSEDSIDGLIEGVRSRIRRLAAEYDLRTFQQPRSVLGGIVSIWQGKPDAWEAIVHGVCSTQNNSKPDWCGNSKTRPSGYAVRKYEDCCWITVFDAGVENTLEDRGFRKIWPRSPQ
>NZ_CP051167.1|WP_168570259.1|4276312_4276627_+|nucleotidyltransferase-family-protein
MSITFRQSKIEIPEAAIAQICQDYHIRKLALFGSILRDDFRPDSDIDILVEFQPGKTPGFGFIDIQDCLSNLLGRTVDLNTPQDLSRYFRDRVVSEAEVIYGER
>NZ_CP051167.1|WP_168570260.1|4276891_4277326_-|hypothetical-protein
MPVCSYELDREVFRLLNSGIEGFDDWQNAARGIADYVASWGVERFWAMSRSQRLLGGQLPSEGVVSEEERRYFAWSVAREVLCKIVGTELGIDYEMNTDNFQEIFRELDFNQQVLLTDLLMEIAEAIQFWTMRLKDARESGTPA
>NZ_CP051167.1|WP_168570261.1|4277421_4278240_-|CRISPR-associated-protein
MRRSKTMAIEWLICREPVHIGGADSSSRGNNNPIYRLSDRTPTIPGSSLRGALREGAEHSSEYQGYVSNWFGGKDENISPGYIALGWGWPVWWPIHVLGYGSWWVSCPAWLNRYQQLSQQNLLNLTEGNIYATDPQFNNQTVYLRWLKLTQIQTCTLSLPAPSEVPPDRRIIVPSDSINLIVDMGLVRQPRVSLNEEPDKKGSLVKNLFAVEGLPPGAVFMTSWTIRNPEKVEQIGEWEKFLRSEHYLGGLWSVGYGRIAIAQTADSTLSQE
>NZ_CP051167.1|WP_168570262.1|4278211_4279255_-|hypothetical-protein
MSELEQSWYSISPAGTVAIGNLTPVGQNSGQVDCRWPPNGHQLAACLNLPTDCTLCGPFWYLSNPGRIYVILPLPVYELERSPQKKKKQKIPPEIFRMVWEENRWQVQSQHRDASIEVVGGRYLISGITLKQLWRDGSRKEPDLQEFPWQKLTLSHNSREEFEVKDEGGFFAEKTTLMDPGWSILVKIIGNYDWQQRLPNPPWSCIGAGATPVSIKREDEEDLTVDWLEGKAESFQGTGAVLLTGALWYEEENFLSVPYPAQVPIAGYAAEVGIPWQSWKSVRDRHNPERKVQVLTPGEWLTPAGAVYLWEGEAPLETSAPLPDRHHRHCLGYGHLWLFEEKQNNGN
>NZ_CP051167.1|WP_168571943.1|4279251_4281507_-|hypothetical-protein
MAIEDWLIQQQQIYQNLPDASPEISIHPVSGEWQTSAYLKSQFWWGGGASIEACRQVAAASNPELTHLGVLSFGPVQEFLGGGERLRDWAVASWLCHYLTAVAIYRWEERQGQVLLPLHRSSPLLNWLRDEPCDRDRFWQAELPNVITGLHPQDETWLQDFNPIITQEWGKFLEALEEEVSQRYSPHLLNGQGWQVIHRDNAYLWSVYTESTPLSLATVSQDIKQLRERIESRKIGRQWQATWWGGRTSPSAGHLSIWHPGLKPIHDGGTWGLPDSQLKEWWLRAANESRDRLSGLVDSDDRLNSIEFVRRLASVPDIIEPTLQLLWGRTPPPCPWGQFPDRATVAAAWVVDRIDAETWNDTLDTLYQCCLDEKPNFRWGMPKVDGKNPPHFAYPRILERRYLKERVPQEKKDTDDEKKIIKDWEDLSQGWESPIEWTVGWRGDGDNMGKWLSGKQYETLKLQWSRWHLNQDAILQHQLNIDPPTLSANATRKLDLPHVLDLSVLFGCWNQLLYPLTERHHNAKVIFAGGDDFLLLGPLTEAVSLTSNLYRLWRGQLSPLTQPLDPPVDGWVKRESEIYPVPGQRMDFSLGVAIAQRRIPQSLWHRGLTEAYKEAKNQGRDRVCIKVLFNSGQSLDWVCPWRLWELLMHVGLTTEEKTELNRWEKLLSYLESNRLQQSDVDTVRDLIETLWASVGIALTWEAIETVAEYDEFDDELGNWSWWIGWISVMGFLARQQREREKWVERVGGNNP

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Crispr_ID: NZ_CP051167_20

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_20

4269452-4271389

TypeIII

N:A

Consensus_repeat	Method
GTTTCAGCACTTTTTCCCTTCAAAGAGGGTCAAAC	PILER-CR
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	CRISPRCasFinder
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	CRT

26 spacers

cas1,cas2,csm3gr7,cas10,csx1

The CRISPR arrays of NZ_CP051167_20

>merge|NZ_CP051167|20|4269452-4271389|PILER-CR,CRISPRCasFinder,CRT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACGGGATACATTCCAACGTACAAGTTCGGAGGGTTGGAAAGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACATCAATACCGACTTCATAGTCGGTTATGAATTGACGATGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACGTCTATGTTGTTGTTGTTGACTGCTCCGAATACCCGGGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACTTGTATAGGGGTTACCGTCCAGCCGAGGGGCTGCGATAACTGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACATCAGCTTCAGACTGTACCTGCATCTGAAACCCATCTGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACATGGCCGACATCCGTCTCCCGTAATACACCAATAGTTGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACTCTGCCCATTCCTCACAGACCGTCACTTGGACGAGAATGGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACATTACCTCGAACTCGAGGCTTACCGTGCTAGTCCCGTGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACTTAATTAGCCCCGATGAACACTCCAAGCGGAGTGCTCGGGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACTGGTGCGGTCCATTTGGGACCAGATAACCTCTTTAGGAATGGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACCTCAGCAGTCGGCCAGCGAAGGGTTTCTTCGCCAGTTGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACACCCAAACCCATTCTGTCGTTTCCTCTTCGCAGTTGGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACTCTGGTGCAATTACTGCACTGAATGACGTGAGGTTCATGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACGAATTAAAATTTCTTGAGCAGAAACACTAGAAACACCGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACGTTTATCACCTTTGGATCCGTCAGGTCGACGGTACCAGGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACGATTTGGGTTAAACGGAACGCCGTTAAAAGTTGTCATGTCGAGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACTCTTGAGTTTCATAACGAACTCCGTTGTTGTACATGCAGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACTAGACTGTATCCAAGGTCGAGGCTGTACTGCTGGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACATTGGAAAAACTTTCCTTGTTCATTTCATGTGGAAATCGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACTGCCCAGGGCAAAAGGCTTGCCCATGGAGAGTGGAGAAGGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACGGGACCCCAGGGTACTGCCCTTGGAGCAATTCCCACAACGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACAATTGCGAGAGCTTGGTTTAGCATGACACCGCCAGAAGGTGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACGAGCTCCACCCTTCCGGGTCGGAGCGAAAAGGTTGTTCGAGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACGGGCCCCTCCGGGCCCTCGACCCACTCCACACAAACTGGGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACGGATCGTCGACTGGGGACGGTTGGGATCAGCAGTAGTGGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAACAGTGCAGTAACCGCATCGGACCCTTCAGAAGCCATCTGTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAG

>NZ_CP051167|20|16|4269452-4271389|PILER-CR
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GGGATACATTCCAACGTACAAGTTCGGAGGGTTGGAAA
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATCAATACCGACTTCATAGTCGGTTATGAATTGACGAT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GTCTATGTTGTTGTTGTTGACTGCTCCGAATACCCGG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TTGTATAGGGGTTACCGTCCAGCCGAGGGGCTGCGATAACT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATCAGCTTCAGACTGTACCTGCATCTGAAACCCATCT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATGGCCGACATCCGTCTCCCGTAATACACCAATAGTT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TCTGCCCATTCCTCACAGACCGTCACTTGGACGAGAATG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATTACCTCGAACTCGAGGCTTACCGTGCTAGTCCCGT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TTAATTAGCCCCGATGAACACTCCAAGCGGAGTGCTCGG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TGGTGCGGTCCATTTGGGACCAGATAACCTCTTTAGGAATG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	CTCAGCAGTCGGCCAGCGAAGGGTTTCTTCGCCAGTT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ACCCAAACCCATTCTGTCGTTTCCTCTTCGCAGTTG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TCTGGTGCAATTACTGCACTGAATGACGTGAGGTTCAT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GAATTAAAATTTCTTGAGCAGAAACACTAGAAACACC
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GTTTATCACCTTTGGATCCGTCAGGTCGACGGTACCAG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GATTTGGGTTAAACGGAACGCCGTTAAAAGTTGTCATGTCGA
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TCTTGAGTTTCATAACGAACTCCGTTGTTGTACATGCA
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TAGACTGTATCCAAGGTCGAGGCTGTACTGCTG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATTGGAAAAACTTTCCTTGTTCATTTCATGTGGAAATC
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TGCCCAGGGCAAAAGGCTTGCCCATGGAGAGTGGAGAAG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GGGACCCCAGGGTACTGCCCTTGGAGCAATTCCCACAAC
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	AATTGCGAGAGCTTGGTTTAGCATGACACCGCCAGAAGGT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GAGCTCCACCCTTCCGGGTCGGAGCGAAAAGGTTGTTCGA
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GGGCCCCTCCGGGCCCTCGACCCACTCCACACAAACTGG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GGATCGTCGACTGGGGACGGTTGGGATCAGCAGTAGTG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	AGTGCAGTAACCGCATCGGACCCTTCAGAAGCCATCT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAG

>NZ_CP051167|20|18|4269452-4271389|CRISPRCasFinder
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GGGATACATTCCAACGTACAAGTTCGGAGGGTTGGAAA
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATCAATACCGACTTCATAGTCGGTTATGAATTGACGAT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GTCTATGTTGTTGTTGTTGACTGCTCCGAATACCCGG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TTGTATAGGGGTTACCGTCCAGCCGAGGGGCTGCGATAACT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATCAGCTTCAGACTGTACCTGCATCTGAAACCCATCT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATGGCCGACATCCGTCTCCCGTAATACACCAATAGTT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TCTGCCCATTCCTCACAGACCGTCACTTGGACGAGAATG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATTACCTCGAACTCGAGGCTTACCGTGCTAGTCCCGT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TTAATTAGCCCCGATGAACACTCCAAGCGGAGTGCTCGG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TGGTGCGGTCCATTTGGGACCAGATAACCTCTTTAGGAATG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	CTCAGCAGTCGGCCAGCGAAGGGTTTCTTCGCCAGTT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ACCCAAACCCATTCTGTCGTTTCCTCTTCGCAGTTG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TCTGGTGCAATTACTGCACTGAATGACGTGAGGTTCAT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GAATTAAAATTTCTTGAGCAGAAACACTAGAAACACC
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GTTTATCACCTTTGGATCCGTCAGGTCGACGGTACCAG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GATTTGGGTTAAACGGAACGCCGTTAAAAGTTGTCATGTCGA
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TCTTGAGTTTCATAACGAACTCCGTTGTTGTACATGCA
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TAGACTGTATCCAAGGTCGAGGCTGTACTGCTG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATTGGAAAAACTTTCCTTGTTCATTTCATGTGGAAATC
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TGCCCAGGGCAAAAGGCTTGCCCATGGAGAGTGGAGAAG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GGGACCCCAGGGTACTGCCCTTGGAGCAATTCCCACAAC
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	AATTGCGAGAGCTTGGTTTAGCATGACACCGCCAGAAGGT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GAGCTCCACCCTTCCGGGTCGGAGCGAAAAGGTTGTTCGA
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GGGCCCCTCCGGGCCCTCGACCCACTCCACACAAACTGG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GGATCGTCGACTGGGGACGGTTGGGATCAGCAGTAGTG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	AGTGCAGTAACCGCATCGGACCCTTCAGAAGCCATCT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAG

>NZ_CP051167|20|9|4269452-4271389|CRT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GGGATACATTCCAACGTACAAGTTCGGAGGGTTGGAAA
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATCAATACCGACTTCATAGTCGGTTATGAATTGACGAT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GTCTATGTTGTTGTTGTTGACTGCTCCGAATACCCGG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TTGTATAGGGGTTACCGTCCAGCCGAGGGGCTGCGATAACT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATCAGCTTCAGACTGTACCTGCATCTGAAACCCATCT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATGGCCGACATCCGTCTCCCGTAATACACCAATAGTT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TCTGCCCATTCCTCACAGACCGTCACTTGGACGAGAATG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATTACCTCGAACTCGAGGCTTACCGTGCTAGTCCCGT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TTAATTAGCCCCGATGAACACTCCAAGCGGAGTGCTCGG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TGGTGCGGTCCATTTGGGACCAGATAACCTCTTTAGGAATG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	CTCAGCAGTCGGCCAGCGAAGGGTTTCTTCGCCAGTT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ACCCAAACCCATTCTGTCGTTTCCTCTTCGCAGTTG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TCTGGTGCAATTACTGCACTGAATGACGTGAGGTTCAT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GAATTAAAATTTCTTGAGCAGAAACACTAGAAACACC
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GTTTATCACCTTTGGATCCGTCAGGTCGACGGTACCAG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GATTTGGGTTAAACGGAACGCCGTTAAAAGTTGTCATGTCGA
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TCTTGAGTTTCATAACGAACTCCGTTGTTGTACATGCA
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TAGACTGTATCCAAGGTCGAGGCTGTACTGCTG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	ATTGGAAAAACTTTCCTTGTTCATTTCATGTGGAAATC
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	TGCCCAGGGCAAAAGGCTTGCCCATGGAGAGTGGAGAAG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GGGACCCCAGGGTACTGCCCTTGGAGCAATTCCCACAAC
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	AATTGCGAGAGCTTGGTTTAGCATGACACCGCCAGAAGGT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GAGCTCCACCCTTCCGGGTCGGAGCGAAAAGGTTGTTCGA
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GGGCCCCTCCGGGCCCTCGACCCACTCCACACAAACTGG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	GGATCGTCGACTGGGGACGGTTGGGATCAGCAGTAGTG
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAC	AGTGCAGTAACCGCATCGGACCCTTCAGAAGCCATCT
GTTTGACCCTCTTTGAAGGGAAAAAGTGCTGAAAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168571943.1\|4279251_4281507_-\|hypothetical-protein	cas10	cd09679_cas10_CAS-III	gnl\|CDD\|187810
NZ_CP051167.1\|WP_168570250.1\|4256313_4258047_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP051167.1\|WP_168570246.1\|4245137_4247498_-\|DUF4131-domain-containing-protein	unknown	unknown	gnl\|CDD\|377126
NZ_CP051167.1\|WP_168570252.1\|4258775_4259138_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570247.1\|4247550_4248024_-\|DUF4079-domain-containing-protein	unknown	unknown	gnl\|CDD\|372553
NZ_CP051167.1\|WP_168570251.1\|4258171_4258723_-\|periplasmic-heavy-metal-sensor	unknown	unknown	gnl\|CDD\|197366
NZ_CP051167.1\|WP_168570254.1\|4262905_4266508_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227922
NZ_CP051167.1\|WP_168570249.1\|4254747_4256214_-\|two-component-sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|223715
NZ_CP051167.1\|WP_168570256.1\|4271487_4272495_+\|CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|272998
NZ_CP051167.1\|WP_168570248.1\|4248100_4249000_-\|glycine--tRNA-ligase-subunit-alpha	unknown	unknown	gnl\|CDD\|236473
NZ_CP051167.1\|WP_168570255.1\|4266670_4268677_+\|CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|376633
NZ_CP051167.1\|WP_168570258.1\|4273153_4274671_+\|hypothetical-protein	csm3gr7	pfam03787_csm3gr7_CAS-III-A:CAS-III-D	gnl\|CDD\|377130
NZ_CP051167.1\|WP_168570262.1\|4278211_4279255_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570253.1\|4259134_4259701_-\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|237124
NZ_CP051167.1\|WP_168570263.1\|4282631_4284095_-\|hypothetical-protein	csx1	mkCas0108_csx1_CAS-III	unknown
NZ_CP051167.1\|WP_168570257.1\|4272558_4272837_+\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP051167.1\|WP_168570260.1\|4276891_4277326_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571816.1\|4281508_4282546_-\|IS630-family-transposase	unknown	unknown	gnl\|CDD\|315923
NZ_CP051167.1\|WP_168570261.1\|4277421_4278240_-\|CRISPR-associated-protein	csm3gr7	pfam03787_csm3gr7_CAS-III-A:CAS-III-D	gnl\|CDD\|224255
NZ_CP051167.1\|WP_168570259.1\|4276312_4276627_+\|nucleotidyltransferase-family-protein	unknown	unknown	gnl\|CDD\|224583

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168571943.1\|4279251_4281507_-\|hypothetical-protein	gnl\|CDD\|187810	cd09679, Cas10_III, CRISPR/Cas system-associated protein Cas10. 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; Multidomain protein with permuted HD nuclease domain, palm domain and Zn-ribbon; MTH326-like has inactivated polymerase catalytic domain; alr1562 and slr7011 - predicted only on the basis of size, presence of HD domain, and location with RAMPs in one operon; signature gene for type III; also known as Crm2 family.	2.46638e-12
NZ_CP051167.1\|WP_168570250.1\|4256313_4258047_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	1.14626e-176
NZ_CP051167.1\|WP_168570246.1\|4245137_4247498_-\|DUF4131-domain-containing-protein	gnl\|CDD\|377126	pfam03772, Competence, Competence protein. Members of this family are integral membrane proteins with 6 predicted transmembrane helices. Some members of this family have been shown to be essential for bacterial competence in uptake of extracellular DNA. These proteins may transport DNA across the cell membrane. These proteins contain a highly conserved motif in the amino terminal transmembrane region that has two histidines that may form a metal binding site.	1.09244e-51
NZ_CP051167.1\|WP_168570247.1\|4247550_4248024_-\|DUF4079-domain-containing-protein	gnl\|CDD\|372553	pfam13301, DUF4079, Protein of unknown function (DUF4079). This is an uncharacterized family of proteins.	5.56196e-36
NZ_CP051167.1\|WP_168570251.1\|4258171_4258723_-\|periplasmic-heavy-metal-sensor	gnl\|CDD\|197366	cd09916, CpxP_like, CpxP component of the bacterial Cpx-two-component system and related proteins. This family summarizes bacterial proteins related to CpxP, a periplasmic protein that forms part of a two-component system which acts as a global modulator of cell-envelope stress in gram-negative bacteria. CpxP aids in combating extracytoplasmic protein-mediated toxicity, and may also be involved in the response to alkaline pH. Functioning as a dimer, it inhibits activation of the kinase CpxA, but also plays a vital role in the quality control system of P pili. It has been suggested that CpxP directly interacts with CpxA via its concave polar surface. Another member of this family, Spy, is also a periplasmic protein that may be involved in the response to stress. The homology between CpxP and Spy suggests similar functions. A characteristic 5-residue sequence motif LTXXQ is found repeated twice in many members of this family.	2.99821e-17
NZ_CP051167.1\|WP_168570254.1\|4262905_4266508_-\|hypothetical-protein	gnl\|CDD\|227922	COG5635, COG5635, Predicted NTPase (NACHT family) [Signal transduction mechanisms].	1.91443e-13
NZ_CP051167.1\|WP_168570249.1\|4254747_4256214_-\|two-component-sensor-histidine-kinase	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	9.52298e-60
NZ_CP051167.1\|WP_168570256.1\|4271487_4272495_+\|CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|272998	TIGR00287, CRISPR-associated_endonuclease_Cas1, CRISPR-associated endonuclease Cas1. This model identifies CRISPR-associated protein Cas1, the most universal CRISPR system protein. CRISPR is an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, a system for heritable host defense by prokaryotic cells against phage and other foreign DNA. Cas1 is a metal-dependent DNA-specific endonuclease.	5.07645e-23
NZ_CP051167.1\|WP_168570248.1\|4248100_4249000_-\|glycine--tRNA-ligase-subunit-alpha	gnl\|CDD\|236473	PRK09348, glyQ, glycyl-tRNA synthetase subunit alpha; Validated.	0
NZ_CP051167.1\|WP_168570255.1\|4266670_4268677_+\|CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|376633	pfam01867, Cas_Cas1, CRISPR associated protein Cas1. Clustered regularly interspaced short palindromic repeats (CRISPRs) are a family of DNA direct repeats found in many prokaryotic genomes. This family of proteins corresponds to Cas1, a CRISPR-associated protein. Cas1 may be involved in linking DNA segments to CRISPR.	1.08231e-113
NZ_CP051167.1\|WP_168570258.1\|4273153_4274671_+\|hypothetical-protein	gnl\|CDD\|377130	pfam03787, RAMPs, RAMP superfamily. The molecular function of these proteins is not yet known. However, they have been identified and called the RAMP (Repair Associated Mysterious Proteins) superfamily. The members of this family have no known function they are around 300 amino acids in length and have several conserved motifs.	3.72196e-09
NZ_CP051167.1\|WP_168570253.1\|4259134_4259701_-\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|237124	PRK12518, PRK12518, RNA polymerase sigma factor; Provisional.	1.03093e-89
NZ_CP051167.1\|WP_168570257.1\|4272558_4272837_+\|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.	4.72875e-25
NZ_CP051167.1\|WP_168571816.1\|4281508_4282546_-\|IS630-family-transposase	gnl\|CDD\|315923	pfam13358, DDE_3, DDE superfamily endonuclease. This family of proteins are related to pfam00665 and are probably endonucleases of the DDE superfamily. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction.	6.61756e-30
NZ_CP051167.1\|WP_168570261.1\|4277421_4278240_-\|CRISPR-associated-protein	gnl\|CDD\|224255	COG1336, COG1336, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	1.98867e-18
NZ_CP051167.1\|WP_168570259.1\|4276312_4276627_+\|nucleotidyltransferase-family-protein	gnl\|CDD\|224583	COG1669, COG1669, Predicted nucleotidyltransferases [General function prediction only].	8.35941e-26

>NZ_CP051167.1|WP_168570255.1|4266670_4268677_+|CRISPR-associated-endonuclease-Cas1
MNFTREQLKAAWQQVRRRSRQAGIDGMTVDRFARDLDEYLSQIQHHLNAETYRALPAKGFYLPKANGGKRSIGIPTVRDRIVQRVLLEELYWPLEETFLDCSYAYRPGRSIHGAARHFSTYTQFQPCWVLKADIAQFFDRLCRSLLLTQLEQLDLEPILVQLLEQQISAGIVIRGQYQNFGQGVLQGAILSGALANLYLTDFDRRSLAAGLNLVRYGDDFAIATSSRRQAQQVLECVGEWLAQVYLTLNPNKTHIYSPDDEFTFLGYRFLGHQFYPPPPPKRPETGEWLLSPSGVPYRRLKPRRTPRVSRPPRGSDSSPMGLPMAHSEHLWSERMTSLYITDQGAYLRVKNQQFEVFYDRQLRVKVPASRVSYIVLFGCCNMSHGAVSLALRRRIPVMFLSQKGRYFGRLYSESHAKVDYLTRQVQCALDSEFTRLQAEAIVAAKLHNSRALLLKLNRRRPTDAAFIALEMLASCRDKLSLAESMDALRGYEGKAASAYFQGLGSLFADPFTFSKRTKRPPTDPINSMMSLGYTLLSQNVHSFVNLAGLHPHFGNLHVPRDNHPALVSDLMEEFRAQIVDSLVAYLVNSKILTPDDFTLPDERNGVYLQPHALKKYLKHWEDKLLSEITHPHTQYKVSLKRCIELQVREYLACLTGEVEVYRPMLWKV
>NZ_CP051167.1|WP_168570254.1|4262905_4266508_-|hypothetical-protein
MSARSLIASHEGIVKAERALKRLNLTRTAIAKEHQIASWSTVSKFFNYKPVDRSFFQEICHLLDLDWQDIAASPDDSQLDDSNADMTDSEKAAQCDRALLDAVIRNGDRTRKALEPYILPTIRRETFLEKCLQQIELGLSGKPRIVPILGAAGYGKSTILGTLYDELTGDREAAWVALVRCDDLLESALSFPEEVGEKASDRRVTIADLAAQLTVEHGRGVLLLDTLDIVLTKTLVPILRALFAELLEWETTVVFTCRHNDYADFFEPYHESFAGFREQVYDGCKLTPFALEEVTLAARLFARLKTEFPTEESQITFADRLLALCADRVSLTEIVCNPLLLALLCELFAEAQVVPEDLTVSQLYEIYWNWKIAKVRHQQQSRRIGKAKEKLCLFLAERLYCHSGERLRDFLYETSLDLTDETDFIAYTALRSDGIVKELGNDRIGFFHQTFLEYAIARWWNGTESGETAQFVIRQELQSPSGQVRHYIWPIFRQFFTLLPLNQFEQISNELDRTQLLPFRAISLAAVSRIEPEATRVLFPLLELAQLRQGAFIETLLIALNSAPQRHDSTVWDLLVKLLSTVGQDALNKTLEIAAVAIARHPEAGARFPEALTALMSHPEIEGDREQGYRFLGKFLNEYYREIRLRDRAIERPVLTALKEYYASLGSKVRSLAIDLYLSEGVPSAVKADFLLTILQLPPANNSFFEREKAIALTVELLPDLLATQSTILGESWLTAFEAPLPTESLGVIAAAVGQHAIDNRQWMAEMVTYLLIDPPSRLSKSFNSNCTIALKEIVQAGGGDRLVKYFLSLEVEQILDNRISTLSTILKTLAQVEGDRLTIDEVLAVQLAQWLRPRLISHPVESIRILDGLAVQFPGVKPILTQGLREIFARTKTRQVNQILKKLHCLPAELAPDLEARQNSKEARIALLKLLRDRAQRGDRESLERTIAFCGDRSQDLAKAASWTVLDLGWENIGIAIESLLPILRDSPIVVVRQNCLKVILEGVNDFGITPTEIAKVLEVMAEEKSPEVLQGMYQLCTAAIWHHPSGERRVEQAIAKAIFKLTRSVLVQAPQMTVDMMANSAWIAFNQMAFLEERSLIPDLLECTHLLWRAIDVRGKIDKTMVTGLLNQLGKYDPQFLEGLVLEAIGEEGNSLPLANWQALVVAIAHNQGKFSPLLDRVIDDPHIPLEVKHRIYQIRDL
>NZ_CP051167.1|WP_168570253.1|4259134_4259701_-|sigma-70-family-RNA-polymerase-sigma-factor
MPTEATETDAELVTRCQEGDRASFRQLYRRYHGKVRSTLYPLCGLSNIDDLVQEVFLRAWKGLPKLKQPAHFGTWLYRISWNVASDRRQAYAKQHQKQERLIGTLPDRDRAGSPETDLMTLHYQDLVKRGLSHLSFDHRSVLVLHDLEDVPQKAIAEILQIPVGTVKSRLFHARSAMRKFLEGEGVQL
>NZ_CP051167.1|WP_168570252.1|4258775_4259138_-|hypothetical-protein
MNQPNDPDRRLVQFLREYAPDVPPPSPELEDRTIDALDGPHPIAVNRAKLRQLRPLWLVPVGIAAGLVVVWNGTRSPIPPQPSAEELAQLETYMETTWDGVLGETSLTESSDWFFPEASE
>NZ_CP051167.1|WP_168570251.1|4258171_4258723_-|periplasmic-heavy-metal-sensor
MKGRMHRRQLCALTALSVLLGTTAAYAAPPEFGNPEIVAQRPGGPGRGRGQGGQRWIEQLDLSQDQQQRIQQIRDRYRSEAESTYTQMMQLRQEMQDLMVGNGSDSQLRSKHDEMMKLHQRMGELRFDQMLEIRAVLSAEQRQQWAQQMQQRHQNRGNRQGNRPGNGRGMGPGGGMDDDFFGE
>NZ_CP051167.1|WP_168570250.1|4256313_4258047_-|ABC-transporter-ATP-binding-protein
MIRSSYGLLLPYLKPQWKTIAQALACTLGFTAFWPILARLAGDMAASIGAGDVATIAQLAGSAAVVFLVRGAVQYGQDALMAKAALAIALDLRQRVYAHLLHLSLGYFSHTQTGDLSYRLTEDIDRIGEVINKIFHQFVPCILQLIVVFSYMIYLNWQLTLASSIVAPLMALSIAWFGEKLRVFSHNSQSRIADLSAIVTEVFGGIRLVQAFCAEDYTLDRFRQAAERNRQARFSAEQLKAIQFPVVGFLEALSVLLLFFLGGWQIAQNNLTGSEFVSYVAAVALSIDPIAITTSNYNEFKQGEASVERVFELLSRQPEVTDKPGAIALPPVKGRIEYRDVTFSYHGKGPYPRPVLQEIDLTVSPGEAIALVGPSGAGKSTLVNLLPRFYDVQSGQVAIDGIDVKSVTLASLRRQIAIVPQETKLFTGTIAENIAFGQLDYDLDRVEAAAKIANAHEFITQMSEGYRSWVGEGGVNLSGGQRQRIAIARAVLLDPTILILDEATSALDSESEGAIQEALDRLMQGRTVLIIAHRLTTVRRCDRIVVLENGQILESGTHGELLAQEGRYAQFHAQQFY
>NZ_CP051167.1|WP_168570249.1|4254747_4256214_-|two-component-sensor-histidine-kinase
MTLIRRWIARPVHWLPKFDPHSLQIRLTVGMALVSALGIGTLAIATSWQMQRQLVATHKQTIKYIFDRFDRDVMHYSERNPAEKGLQPAIDSLSADRVLLWVKRPDGAIAAQSMPLSGRDDDTSKGLLGLPARQMMPQVSEIGGRFWVWCSGPLTVKGTHLGQLYIAADITEDRGILEGLIRTLALASGAAIVAMTVAIALYVRRSLRPVLEIGQLADRISVRELDTARIQLQNAPSEVRQLAQTCNTMLDRLAQSWEQQRQFVSNVSHELRTPLTLVSGYLQSTLRRATNLSEPQREALEIAASEAERTIQLLQDLLDLARADRGYLHFQLEPLLIVDLVAEVVEMAKQYSHREIAIVCGEDLLEASADRNRLKQVLLNLIDNAVKYSPSDTEIKVGVRSFGDRAIVEICDRGVGIPLAQQGRIFERFYRVDEARSRSVSPGESLATGGTGLGLSIVKTLVEGMGGTVTVRSKPGEGSTFGVILQRD
>NZ_CP051167.1|WP_168570248.1|4248100_4249000_-|glycine--tRNA-ligase-subunit-alpha
MNFQSLVATLNQFWSDRGCLIAQPYDMEKGAGTMNPHTFLRAIGPEPWSVAYIEPCRRPTDGRYGENPNRYQHYYQYQVLLKPSPNNIQEIYLDSLRALGIAPEDHDIRFVEDNWEAPTVAAWGVGWEVWLDGMEITQFTYFQQCGGIDCRPVSIEITYGLERLAMYLQNIDAMAKIAWTDDIRYGDVHLQGEIEQCTYNFEASNPELLFTLFGLYEQEAQQLVDRGLVLPTLDYVLKCSHTFNLLDARGVIAVTERTRYIGRIRHLARRVAQLYLEQREALGFPLLNSSTPTETASAA
>NZ_CP051167.1|WP_168570247.1|4247550_4248024_-|DUF4079-domain-containing-protein
MDLTQILEPIASQFRNLGIPEPIVHWGHPLMMGIVVFVMGSYVGWSGWRARVVGAGETAVQSRSDHRKLAPWMFLFMALGYTGGLLSLVMQREPILESPHFWTGSIALILLGINSILSLNFGDDRPNLRTAHAYLGSIVLGLIVLHALLGLKLGLSL
>NZ_CP051167.1|WP_168570246.1|4245137_4247498_-|DUF4131-domain-containing-protein
MTAAPLILLCLAYIAGLLASAIPGGRYGLLVLGIGAGIGVFLKLPGYLRCLKAGLKPAFFIAAGALALIAAFYLQLRLPQPQTDDISHYIAPTTGIGEQPAVTVLGKVTSTPRLTRSNKVQFWFDVTQLNELVGSADPIATVPPTSRTQPVSGKLYVTVPLLQGTGVHPGRRLSISGELYKPEPPKNPGAFDFQAYLASRGSFAGLRGEQVYFLSETREEGWGLWRVQRRIVRSQVRWLGVPHGPLVSAIVLGRRVVDLSIEVRDRFIQVGLAHVLAASGFHVALILSLVRLLTRPLSERLQFGAGSAVLMLYVILTGGSASVSRAAIMGFAALLAPLLQKQVKPLGSLLLAATILLLLQPGWIWDLGFQLSFLATLGLLVTVPSIVERLDWLPVTIASALAVPIAATIWTLPLQLYVFHVVSPYSIAVNLITTPLVSAITIGGFISAIAGAIWPLAGSALAWLLYYPVEGLLEIVEFFANLPGNSVATGALSIAQVVLLYTTIAAIWVIPWLQRQRRWGLGVLFAIALVVTPTLHAKATVVQMTVLATPRDPVLVIQNRGQVALVNSGDDRTTQFTILPFFRQQAIARLDWAISTAPVSSNTGWHQLFDRLDIALFSAPEPSPEEGDLLSHEAILHDLEQFEGSYEPLREDETLKFGAIAVRPISFEPMVVELQFDGQTWLWLGNLDPSQQNRWLGAGILPGSRPESSLDVLWWSGDQVTPYLLDALQPEVAIAASEEIDPATATLLEQKNIRIYITGLEGAVRWTPTQGFESHGAIAEDRIPWI
>NZ_CP051167.1|WP_168570256.1|4271487_4272495_+|CRISPR-associated-endonuclease-Cas1
MTAIYLTQPGSLLDAKRGVFELWHDDRRQRRIPAKLTSQILVFEDSQLSKTAIALAISFRLPVLFLDRHHRHLGRLHLNPNSGSQHRSRPGTPDPDDRRDLAERLVSAILNSRQSLLNTLDGAICPTVELTRGTIARILDELPTASGDRLREHLTGVDRLYYPALRQWLRLSAGTVLAPIDPWFYLAHSLLEQVTYGFVLDAGVNPYESILHCDTGDNLPLVRDLMLEWTVTLVDLLVLRFCMDEFLFSGNGNGSHSPLSRLRDRFVQQWETQLASEAIAGTSYRQCLFAQVRRYREALWGDRLYSPVLLRSESFVSGQPLRALRSRRSPCTHLT
>NZ_CP051167.1|WP_168570257.1|4272558_4272837_+|CRISPR-associated-endonuclease-Cas2
MLYLVCYDITKDSRRVRVAKLLETYGMRVQQSVFELVLNEQQYATLEKRLVKLLDRREDQLRFYPLPPQVRDRVTILGVRSPFAIDDPTIIV
>NZ_CP051167.1|WP_168570258.1|4273153_4274671_+|hypothetical-protein
MNLPLPTSLPRWYTVKENEEKGWTPETDDIVDKPENREITQAWNGSFCPPEASQFTLRLNNLQVISPVQVGGGSFREGHILPAQFGGIPCIPGSSIRGALLKWMRRIWSDLPPDEQAFWNKLIEGDRSGWQPRQIRFESLFLKKHLKPFPLYAQQSWQVFDTRSNQLGVQWQVSPVLPPTSPPKFSIQVLLSQEATESEKSWLRNRLEEMLKEQGLGRGTASGFGRMARSLPLTATWEIALTGTKPAIQQQDNKENIVGKYRWSPQVLRATLRGYFTRVALSLLSRNDAETLTSKIFGGLNSPARLTLTSYLTQCQRSPTAGTNYANIPAKDAHSTWIIRADCTPEFQDLIDPLLNIASRIGGLGPGWRRPPHSFRNNSLFRGSEFTLTPKSEDSIDGLIEGVRSRIRRLAAEYDLRTFQQPRSVLGGIVSIWQGKPDAWEAIVHGVCSTQNNSKPDWCGNSKTRPSGYAVRKYEDCCWITVFDAGVENTLEDRGFRKIWPRSPQ
>NZ_CP051167.1|WP_168570259.1|4276312_4276627_+|nucleotidyltransferase-family-protein
MSITFRQSKIEIPEAAIAQICQDYHIRKLALFGSILRDDFRPDSDIDILVEFQPGKTPGFGFIDIQDCLSNLLGRTVDLNTPQDLSRYFRDRVVSEAEVIYGER
>NZ_CP051167.1|WP_168570260.1|4276891_4277326_-|hypothetical-protein
MPVCSYELDREVFRLLNSGIEGFDDWQNAARGIADYVASWGVERFWAMSRSQRLLGGQLPSEGVVSEEERRYFAWSVAREVLCKIVGTELGIDYEMNTDNFQEIFRELDFNQQVLLTDLLMEIAEAIQFWTMRLKDARESGTPA
>NZ_CP051167.1|WP_168570261.1|4277421_4278240_-|CRISPR-associated-protein
MRRSKTMAIEWLICREPVHIGGADSSSRGNNNPIYRLSDRTPTIPGSSLRGALREGAEHSSEYQGYVSNWFGGKDENISPGYIALGWGWPVWWPIHVLGYGSWWVSCPAWLNRYQQLSQQNLLNLTEGNIYATDPQFNNQTVYLRWLKLTQIQTCTLSLPAPSEVPPDRRIIVPSDSINLIVDMGLVRQPRVSLNEEPDKKGSLVKNLFAVEGLPPGAVFMTSWTIRNPEKVEQIGEWEKFLRSEHYLGGLWSVGYGRIAIAQTADSTLSQE
>NZ_CP051167.1|WP_168570262.1|4278211_4279255_-|hypothetical-protein
MSELEQSWYSISPAGTVAIGNLTPVGQNSGQVDCRWPPNGHQLAACLNLPTDCTLCGPFWYLSNPGRIYVILPLPVYELERSPQKKKKQKIPPEIFRMVWEENRWQVQSQHRDASIEVVGGRYLISGITLKQLWRDGSRKEPDLQEFPWQKLTLSHNSREEFEVKDEGGFFAEKTTLMDPGWSILVKIIGNYDWQQRLPNPPWSCIGAGATPVSIKREDEEDLTVDWLEGKAESFQGTGAVLLTGALWYEEENFLSVPYPAQVPIAGYAAEVGIPWQSWKSVRDRHNPERKVQVLTPGEWLTPAGAVYLWEGEAPLETSAPLPDRHHRHCLGYGHLWLFEEKQNNGN
>NZ_CP051167.1|WP_168571943.1|4279251_4281507_-|hypothetical-protein
MAIEDWLIQQQQIYQNLPDASPEISIHPVSGEWQTSAYLKSQFWWGGGASIEACRQVAAASNPELTHLGVLSFGPVQEFLGGGERLRDWAVASWLCHYLTAVAIYRWEERQGQVLLPLHRSSPLLNWLRDEPCDRDRFWQAELPNVITGLHPQDETWLQDFNPIITQEWGKFLEALEEEVSQRYSPHLLNGQGWQVIHRDNAYLWSVYTESTPLSLATVSQDIKQLRERIESRKIGRQWQATWWGGRTSPSAGHLSIWHPGLKPIHDGGTWGLPDSQLKEWWLRAANESRDRLSGLVDSDDRLNSIEFVRRLASVPDIIEPTLQLLWGRTPPPCPWGQFPDRATVAAAWVVDRIDAETWNDTLDTLYQCCLDEKPNFRWGMPKVDGKNPPHFAYPRILERRYLKERVPQEKKDTDDEKKIIKDWEDLSQGWESPIEWTVGWRGDGDNMGKWLSGKQYETLKLQWSRWHLNQDAILQHQLNIDPPTLSANATRKLDLPHVLDLSVLFGCWNQLLYPLTERHHNAKVIFAGGDDFLLLGPLTEAVSLTSNLYRLWRGQLSPLTQPLDPPVDGWVKRESEIYPVPGQRMDFSLGVAIAQRRIPQSLWHRGLTEAYKEAKNQGRDRVCIKVLFNSGQSLDWVCPWRLWELLMHVGLTTEEKTELNRWEKLLSYLESNRLQQSDVDTVRDLIETLWASVGIALTWEAIETVAEYDEFDDELGNWSWWIGWISVMGFLARQQREREKWVERVGGNNP
>NZ_CP051167.1|WP_168571816.1|4281508_4282546_-|IS630-family-transposase
MNIIDELDNFIENTTNTKEMKRALAAKMKLSGQPSKKIEEILNVSSSFVSQWKNKAIFEGVESLNLQYKGSKGYLKPEEKTQITSWIRQQEYLRLSDLKRYLQQEYNVIYSSNQSYYDLLKAAGMSWKKSQKKNPAKDEKLVKKKEEEIQKKLKDWEEDIKAGKLAVFMIDECHLLWGDVLGFVWGRKDIRVEIPIKNQKSRQSYYGALDYQTHEFILQEYPKADTDNTIQFIQYLREQRPGQKLAIFWDGARYHDSQQFRDFLKELNEGLEEDEWLITCTKFAPNAPEQNPVEDIWLQTKNFLRTFYFLCDSFKRVKELFKIFADGQVFDFPKLYSYGFLPQMT
>NZ_CP051167.1|WP_168570263.1|4282631_4284095_-|hypothetical-protein
MTTLILQVLGNSDITSGDLKGWETLTESDSLKGIERRAGINSKKFCEGKTDFDFPLIRKLITATEGVNSSTALFCFILTDQTDWQSQRSETGQGWANIVAKDGIWWKEILAKWCDKNNIKQYSVRFKIEPNLLNGTADWEGMAEKIEKLFKILINFEGDYIYFQPTKEESILIDKIIVQHSSGTPALNGALYLWGIERKLTVKSIDFVYISEEQLECEPHSGTHWQWHLKVPQIRELLKIQDFSGALQILKSHPHSIEEIKTKLQELDRAVSLNLTGRENLTGREGIIERVAIAVWSETAFRDRSQWMHWYLRVAGAFELAILLLIEKQGNGDYEWQGIKLLDPDQKDISPCSIAAIVYPLLTKGVWEYISPKKEIHQFTIAPVTDCNWVKFKKFYVDIWELESKPKTTQAFTSIRNKLYHSLLGDRIDELLDKKTEELGSVTHEKHPAQVAVDYLHYIIDLAGLTDEVQERATTYREIVENIEENL

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Crispr_ID: NZ_CP051167_21

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_21

4274885-4276240

TypeIII

N:A

Consensus_repeat	Method
GTTTCAGCACCTTTTCCTTCTAATGAAGGTCGATCGC	PILER-CR
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	CRISPRCasFinder
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	CRT

18 spacers

csm3gr7,cas2,cas1,cas10,csx1

The CRISPR arrays of NZ_CP051167_21

>merge|NZ_CP051167|21|4274885-4276240|PILER-CR,CRISPRCasFinder,CRT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACCTTGTGGCTGGAATGTAGAATACCTTCTTCTCTGAAGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACCCACATTTGGTCTACATCCGGGGGGATGTAGTTTTTGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACTACAACGTTGAAGTCAGTTTCCAACTGACGGAAGGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACAATCAAAGCTTGGTTCGAGACCAATCGATAATTCCTAGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACTTCAACCCAAGATCCTCGTCGATTTCCAATCGAACGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACTCAACCCCATAGCAATCCGCCAGCACGGTTAATTGGTCTGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACGGGTTCTTGCCCGACAAACTAGAGGTAATCTCTAGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACAGATAGATACTCTCTTGGGCTAGTAATCTCAACCCTTGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACTTTCTCAAGGATTATTTGATTTAATTATTTGGGTAGGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACACTCGCAATCGCTTCGAGCGATAGATCTTCTTGGCAGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACAAGTATATGAACCTAGTCGATCTTCTAATGATTGATTCGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACGAATCCCATATTCTAGGTCTCTTCTTCCAATAATCTGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACCTTGTGTCGGGACAACACCTCCTCTAGTTGCTGCGGGGGAGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACTTCAGGAAAGTTGCGAACCTTTGGCCGCTAAGTTTACGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACCTTATATACTTTCTTATCAACTGAGGCGGCGCTCAAGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACAATCCACTCTAGAGGGAGAGTGCAGAAGTAACCATGTGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACAGCAGTTCGACGCTATGTGGCGCTGGAGAAACAGCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAACATCTTTGATATCTGCCCTTTCCCATCCTTTAAGGTTCGTAGCGATCTTCGTTAGAAGGAAAATGTGCTGAAAC

>NZ_CP051167|21|17|4274885-4276167|PILER-CR
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	CTTGTGGCTGGAATGTAGAATACCTTCTTCTCTGAA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	CCACATTTGGTCTACATCCGGGGGGATGTAGTTTTT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TACAACGTTGAAGTCAGTTTCCAACTGACGGAAG
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AATCAAAGCTTGGTTCGAGACCAATCGATAATTCCTA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TTCAACCCAAGATCCTCGTCGATTTCCAATCGAAC
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TCAACCCCATAGCAATCCGCCAGCACGGTTAATTGGTCT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	GGGTTCTTGCCCGACAAACTAGAGGTAATCTCTA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AGATAGATACTCTCTTGGGCTAGTAATCTCAACCCTT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TTTCTCAAGGATTATTTGATTTAATTATTTGGGTAG
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	ACTCGCAATCGCTTCGAGCGATAGATCTTCTTGGCA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AAGTATATGAACCTAGTCGATCTTCTAATGATTGATTC
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	GAATCCCATATTCTAGGTCTCTTCTTCCAATAATCT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	CTTGTGTCGGGACAACACCTCCTCTAGTTGCTGCGGGGGA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TTCAGGAAAGTTGCGAACCTTTGGCCGCTAAGTTTAC
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	CTTATATACTTTCTTATCAACTGAGGCGGCGCTCAA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AATCCACTCTAGAGGGAGAGTGCAGAAGTAACCATGT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AGCAGTTCGACGCTATGTGGCGCTGGAGAAACA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC

>NZ_CP051167|21|19|4274885-4276240|CRISPRCasFinder
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	CTTGTGGCTGGAATGTAGAATACCTTCTTCTCTGAA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	CCACATTTGGTCTACATCCGGGGGGATGTAGTTTTT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TACAACGTTGAAGTCAGTTTCCAACTGACGGAAG
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AATCAAAGCTTGGTTCGAGACCAATCGATAATTCCTA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TTCAACCCAAGATCCTCGTCGATTTCCAATCGAAC
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TCAACCCCATAGCAATCCGCCAGCACGGTTAATTGGTCT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	GGGTTCTTGCCCGACAAACTAGAGGTAATCTCTA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AGATAGATACTCTCTTGGGCTAGTAATCTCAACCCTT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TTTCTCAAGGATTATTTGATTTAATTATTTGGGTAG
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	ACTCGCAATCGCTTCGAGCGATAGATCTTCTTGGCA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AAGTATATGAACCTAGTCGATCTTCTAATGATTGATTC
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	GAATCCCATATTCTAGGTCTCTTCTTCCAATAATCT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	CTTGTGTCGGGACAACACCTCCTCTAGTTGCTGCGGGGGA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TTCAGGAAAGTTGCGAACCTTTGGCCGCTAAGTTTAC
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	CTTATATACTTTCTTATCAACTGAGGCGGCGCTCAA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AATCCACTCTAGAGGGAGAGTGCAGAAGTAACCATGT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AGCAGTTCGACGCTATGTGGCGCTGGAGAAACA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	ATCTTTGATATCTGCCCTTTCCCATCCTTTAAGGTT
CGTAGCGATCTTCGTTAGAAGGAAAATGTGCTGAAAC

>NZ_CP051167|21|10|4274885-4276240|CRT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	CTTGTGGCTGGAATGTAGAATACCTTCTTCTCTGAA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	CCACATTTGGTCTACATCCGGGGGGATGTAGTTTTT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TACAACGTTGAAGTCAGTTTCCAACTGACGGAAG
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AATCAAAGCTTGGTTCGAGACCAATCGATAATTCCTA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TTCAACCCAAGATCCTCGTCGATTTCCAATCGAAC
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TCAACCCCATAGCAATCCGCCAGCACGGTTAATTGGTCT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	GGGTTCTTGCCCGACAAACTAGAGGTAATCTCTA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AGATAGATACTCTCTTGGGCTAGTAATCTCAACCCTT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TTTCTCAAGGATTATTTGATTTAATTATTTGGGTAG
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	ACTCGCAATCGCTTCGAGCGATAGATCTTCTTGGCA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AAGTATATGAACCTAGTCGATCTTCTAATGATTGATTC
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	GAATCCCATATTCTAGGTCTCTTCTTCCAATAATCT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	CTTGTGTCGGGACAACACCTCCTCTAGTTGCTGCGGGGGA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	TTCAGGAAAGTTGCGAACCTTTGGCCGCTAAGTTTAC
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	CTTATATACTTTCTTATCAACTGAGGCGGCGCTCAA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AATCCACTCTAGAGGGAGAGTGCAGAAGTAACCATGT
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	AGCAGTTCGACGCTATGTGGCGCTGGAGAAACA
GCGATCGACCTTCATTAGAAGGAAAAGGTGCTGAAAC	ATCTTTGATATCTGCCCTTTCCCATCCTTTAAGGTT
CGTAGCGATCTTCGTTAGAAGGAAAATGTGCTGAAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168571943.1\|4279251_4281507_-\|hypothetical-protein	cas10	cd09679_cas10_CAS-III	gnl\|CDD\|187810
NZ_CP051167.1\|WP_168570250.1\|4256313_4258047_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP051167.1\|WP_168570264.1\|4284162_4286073_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|375164
NZ_CP051167.1\|WP_168570252.1\|4258775_4259138_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570259.1\|4276312_4276627_+\|nucleotidyltransferase-family-protein	unknown	unknown	gnl\|CDD\|224583
NZ_CP051167.1\|WP_168570251.1\|4258171_4258723_-\|periplasmic-heavy-metal-sensor	unknown	unknown	gnl\|CDD\|197366
NZ_CP051167.1\|WP_168570254.1\|4262905_4266508_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227922
NZ_CP051167.1\|WP_168570249.1\|4254747_4256214_-\|two-component-sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|223715
NZ_CP051167.1\|WP_168570256.1\|4271487_4272495_+\|CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|272998
NZ_CP051167.1\|WP_168570255.1\|4266670_4268677_+\|CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|376633
NZ_CP051167.1\|WP_168570266.1\|4288325_4289819_-\|glycosyltransferase-family-2-protein	unknown	unknown	gnl\|CDD\|366154
NZ_CP051167.1\|WP_168570258.1\|4273153_4274671_+\|hypothetical-protein	csm3gr7	pfam03787_csm3gr7_CAS-III-A:CAS-III-D	gnl\|CDD\|377130
NZ_CP051167.1\|WP_168570262.1\|4278211_4279255_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570253.1\|4259134_4259701_-\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|237124
NZ_CP051167.1\|WP_168570263.1\|4282631_4284095_-\|hypothetical-protein	csx1	mkCas0108_csx1_CAS-III	unknown
NZ_CP051167.1\|WP_168570257.1\|4272558_4272837_+\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP051167.1\|WP_168571816.1\|4281508_4282546_-\|IS630-family-transposase	unknown	unknown	gnl\|CDD\|315923
NZ_CP051167.1\|WP_168570265.1\|4287178_4288261_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP051167.1\|WP_168570261.1\|4277421_4278240_-\|CRISPR-associated-protein	csm3gr7	pfam03787_csm3gr7_CAS-III-A:CAS-III-D	gnl\|CDD\|224255
NZ_CP051167.1\|WP_168570260.1\|4276891_4277326_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168571943.1\|4279251_4281507_-\|hypothetical-protein	gnl\|CDD\|187810	cd09679, Cas10_III, CRISPR/Cas system-associated protein Cas10. 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; Multidomain protein with permuted HD nuclease domain, palm domain and Zn-ribbon; MTH326-like has inactivated polymerase catalytic domain; alr1562 and slr7011 - predicted only on the basis of size, presence of HD domain, and location with RAMPs in one operon; signature gene for type III; also known as Crm2 family.	2.46638e-12
NZ_CP051167.1\|WP_168570250.1\|4256313_4258047_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	1.14626e-176
NZ_CP051167.1\|WP_168570264.1\|4284162_4286073_-\|hypothetical-protein	gnl\|CDD\|375164	pfam17380, DUF5401, Family of unknown function (DUF5401). This is a family of unknown function found in Chromadorea.	0.000417493
NZ_CP051167.1\|WP_168570259.1\|4276312_4276627_+\|nucleotidyltransferase-family-protein	gnl\|CDD\|224583	COG1669, COG1669, Predicted nucleotidyltransferases [General function prediction only].	8.35941e-26
NZ_CP051167.1\|WP_168570251.1\|4258171_4258723_-\|periplasmic-heavy-metal-sensor	gnl\|CDD\|197366	cd09916, CpxP_like, CpxP component of the bacterial Cpx-two-component system and related proteins. This family summarizes bacterial proteins related to CpxP, a periplasmic protein that forms part of a two-component system which acts as a global modulator of cell-envelope stress in gram-negative bacteria. CpxP aids in combating extracytoplasmic protein-mediated toxicity, and may also be involved in the response to alkaline pH. Functioning as a dimer, it inhibits activation of the kinase CpxA, but also plays a vital role in the quality control system of P pili. It has been suggested that CpxP directly interacts with CpxA via its concave polar surface. Another member of this family, Spy, is also a periplasmic protein that may be involved in the response to stress. The homology between CpxP and Spy suggests similar functions. A characteristic 5-residue sequence motif LTXXQ is found repeated twice in many members of this family.	2.99821e-17
NZ_CP051167.1\|WP_168570254.1\|4262905_4266508_-\|hypothetical-protein	gnl\|CDD\|227922	COG5635, COG5635, Predicted NTPase (NACHT family) [Signal transduction mechanisms].	1.91443e-13
NZ_CP051167.1\|WP_168570249.1\|4254747_4256214_-\|two-component-sensor-histidine-kinase	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	9.52298e-60
NZ_CP051167.1\|WP_168570256.1\|4271487_4272495_+\|CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|272998	TIGR00287, CRISPR-associated_endonuclease_Cas1, CRISPR-associated endonuclease Cas1. This model identifies CRISPR-associated protein Cas1, the most universal CRISPR system protein. CRISPR is an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, a system for heritable host defense by prokaryotic cells against phage and other foreign DNA. Cas1 is a metal-dependent DNA-specific endonuclease.	5.07645e-23
NZ_CP051167.1\|WP_168570255.1\|4266670_4268677_+\|CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|376633	pfam01867, Cas_Cas1, CRISPR associated protein Cas1. Clustered regularly interspaced short palindromic repeats (CRISPRs) are a family of DNA direct repeats found in many prokaryotic genomes. This family of proteins corresponds to Cas1, a CRISPR-associated protein. Cas1 may be involved in linking DNA segments to CRISPR.	1.08231e-113
NZ_CP051167.1\|WP_168570266.1\|4288325_4289819_-\|glycosyltransferase-family-2-protein	gnl\|CDD\|366154	pfam00535, Glycos_transf_2, Glycosyl transferase family 2. Diverse family, transferring sugar from UDP-glucose, UDP-N-acetyl- galactosamine, GDP-mannose or CDP-abequose, to a range of substrates including cellulose, dolichol phosphate and teichoic acids.	2.08127e-30
NZ_CP051167.1\|WP_168570258.1\|4273153_4274671_+\|hypothetical-protein	gnl\|CDD\|377130	pfam03787, RAMPs, RAMP superfamily. The molecular function of these proteins is not yet known. However, they have been identified and called the RAMP (Repair Associated Mysterious Proteins) superfamily. The members of this family have no known function they are around 300 amino acids in length and have several conserved motifs.	3.72196e-09
NZ_CP051167.1\|WP_168570253.1\|4259134_4259701_-\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|237124	PRK12518, PRK12518, RNA polymerase sigma factor; Provisional.	1.03093e-89
NZ_CP051167.1\|WP_168570257.1\|4272558_4272837_+\|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.	4.72875e-25
NZ_CP051167.1\|WP_168571816.1\|4281508_4282546_-\|IS630-family-transposase	gnl\|CDD\|315923	pfam13358, DDE_3, DDE superfamily endonuclease. This family of proteins are related to pfam00665 and are probably endonucleases of the DDE superfamily. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction.	6.61756e-30
NZ_CP051167.1\|WP_168570265.1\|4287178_4288261_+\|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.	7.16752e-28
NZ_CP051167.1\|WP_168570261.1\|4277421_4278240_-\|CRISPR-associated-protein	gnl\|CDD\|224255	COG1336, COG1336, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	1.98867e-18

>NZ_CP051167.1|WP_168570258.1|4273153_4274671_+|hypothetical-protein
MNLPLPTSLPRWYTVKENEEKGWTPETDDIVDKPENREITQAWNGSFCPPEASQFTLRLNNLQVISPVQVGGGSFREGHILPAQFGGIPCIPGSSIRGALLKWMRRIWSDLPPDEQAFWNKLIEGDRSGWQPRQIRFESLFLKKHLKPFPLYAQQSWQVFDTRSNQLGVQWQVSPVLPPTSPPKFSIQVLLSQEATESEKSWLRNRLEEMLKEQGLGRGTASGFGRMARSLPLTATWEIALTGTKPAIQQQDNKENIVGKYRWSPQVLRATLRGYFTRVALSLLSRNDAETLTSKIFGGLNSPARLTLTSYLTQCQRSPTAGTNYANIPAKDAHSTWIIRADCTPEFQDLIDPLLNIASRIGGLGPGWRRPPHSFRNNSLFRGSEFTLTPKSEDSIDGLIEGVRSRIRRLAAEYDLRTFQQPRSVLGGIVSIWQGKPDAWEAIVHGVCSTQNNSKPDWCGNSKTRPSGYAVRKYEDCCWITVFDAGVENTLEDRGFRKIWPRSPQ
>NZ_CP051167.1|WP_168570257.1|4272558_4272837_+|CRISPR-associated-endonuclease-Cas2
MLYLVCYDITKDSRRVRVAKLLETYGMRVQQSVFELVLNEQQYATLEKRLVKLLDRREDQLRFYPLPPQVRDRVTILGVRSPFAIDDPTIIV
>NZ_CP051167.1|WP_168570256.1|4271487_4272495_+|CRISPR-associated-endonuclease-Cas1
MTAIYLTQPGSLLDAKRGVFELWHDDRRQRRIPAKLTSQILVFEDSQLSKTAIALAISFRLPVLFLDRHHRHLGRLHLNPNSGSQHRSRPGTPDPDDRRDLAERLVSAILNSRQSLLNTLDGAICPTVELTRGTIARILDELPTASGDRLREHLTGVDRLYYPALRQWLRLSAGTVLAPIDPWFYLAHSLLEQVTYGFVLDAGVNPYESILHCDTGDNLPLVRDLMLEWTVTLVDLLVLRFCMDEFLFSGNGNGSHSPLSRLRDRFVQQWETQLASEAIAGTSYRQCLFAQVRRYREALWGDRLYSPVLLRSESFVSGQPLRALRSRRSPCTHLT
>NZ_CP051167.1|WP_168570255.1|4266670_4268677_+|CRISPR-associated-endonuclease-Cas1
MNFTREQLKAAWQQVRRRSRQAGIDGMTVDRFARDLDEYLSQIQHHLNAETYRALPAKGFYLPKANGGKRSIGIPTVRDRIVQRVLLEELYWPLEETFLDCSYAYRPGRSIHGAARHFSTYTQFQPCWVLKADIAQFFDRLCRSLLLTQLEQLDLEPILVQLLEQQISAGIVIRGQYQNFGQGVLQGAILSGALANLYLTDFDRRSLAAGLNLVRYGDDFAIATSSRRQAQQVLECVGEWLAQVYLTLNPNKTHIYSPDDEFTFLGYRFLGHQFYPPPPPKRPETGEWLLSPSGVPYRRLKPRRTPRVSRPPRGSDSSPMGLPMAHSEHLWSERMTSLYITDQGAYLRVKNQQFEVFYDRQLRVKVPASRVSYIVLFGCCNMSHGAVSLALRRRIPVMFLSQKGRYFGRLYSESHAKVDYLTRQVQCALDSEFTRLQAEAIVAAKLHNSRALLLKLNRRRPTDAAFIALEMLASCRDKLSLAESMDALRGYEGKAASAYFQGLGSLFADPFTFSKRTKRPPTDPINSMMSLGYTLLSQNVHSFVNLAGLHPHFGNLHVPRDNHPALVSDLMEEFRAQIVDSLVAYLVNSKILTPDDFTLPDERNGVYLQPHALKKYLKHWEDKLLSEITHPHTQYKVSLKRCIELQVREYLACLTGEVEVYRPMLWKV
>NZ_CP051167.1|WP_168570254.1|4262905_4266508_-|hypothetical-protein
MSARSLIASHEGIVKAERALKRLNLTRTAIAKEHQIASWSTVSKFFNYKPVDRSFFQEICHLLDLDWQDIAASPDDSQLDDSNADMTDSEKAAQCDRALLDAVIRNGDRTRKALEPYILPTIRRETFLEKCLQQIELGLSGKPRIVPILGAAGYGKSTILGTLYDELTGDREAAWVALVRCDDLLESALSFPEEVGEKASDRRVTIADLAAQLTVEHGRGVLLLDTLDIVLTKTLVPILRALFAELLEWETTVVFTCRHNDYADFFEPYHESFAGFREQVYDGCKLTPFALEEVTLAARLFARLKTEFPTEESQITFADRLLALCADRVSLTEIVCNPLLLALLCELFAEAQVVPEDLTVSQLYEIYWNWKIAKVRHQQQSRRIGKAKEKLCLFLAERLYCHSGERLRDFLYETSLDLTDETDFIAYTALRSDGIVKELGNDRIGFFHQTFLEYAIARWWNGTESGETAQFVIRQELQSPSGQVRHYIWPIFRQFFTLLPLNQFEQISNELDRTQLLPFRAISLAAVSRIEPEATRVLFPLLELAQLRQGAFIETLLIALNSAPQRHDSTVWDLLVKLLSTVGQDALNKTLEIAAVAIARHPEAGARFPEALTALMSHPEIEGDREQGYRFLGKFLNEYYREIRLRDRAIERPVLTALKEYYASLGSKVRSLAIDLYLSEGVPSAVKADFLLTILQLPPANNSFFEREKAIALTVELLPDLLATQSTILGESWLTAFEAPLPTESLGVIAAAVGQHAIDNRQWMAEMVTYLLIDPPSRLSKSFNSNCTIALKEIVQAGGGDRLVKYFLSLEVEQILDNRISTLSTILKTLAQVEGDRLTIDEVLAVQLAQWLRPRLISHPVESIRILDGLAVQFPGVKPILTQGLREIFARTKTRQVNQILKKLHCLPAELAPDLEARQNSKEARIALLKLLRDRAQRGDRESLERTIAFCGDRSQDLAKAASWTVLDLGWENIGIAIESLLPILRDSPIVVVRQNCLKVILEGVNDFGITPTEIAKVLEVMAEEKSPEVLQGMYQLCTAAIWHHPSGERRVEQAIAKAIFKLTRSVLVQAPQMTVDMMANSAWIAFNQMAFLEERSLIPDLLECTHLLWRAIDVRGKIDKTMVTGLLNQLGKYDPQFLEGLVLEAIGEEGNSLPLANWQALVVAIAHNQGKFSPLLDRVIDDPHIPLEVKHRIYQIRDL
>NZ_CP051167.1|WP_168570253.1|4259134_4259701_-|sigma-70-family-RNA-polymerase-sigma-factor
MPTEATETDAELVTRCQEGDRASFRQLYRRYHGKVRSTLYPLCGLSNIDDLVQEVFLRAWKGLPKLKQPAHFGTWLYRISWNVASDRRQAYAKQHQKQERLIGTLPDRDRAGSPETDLMTLHYQDLVKRGLSHLSFDHRSVLVLHDLEDVPQKAIAEILQIPVGTVKSRLFHARSAMRKFLEGEGVQL
>NZ_CP051167.1|WP_168570252.1|4258775_4259138_-|hypothetical-protein
MNQPNDPDRRLVQFLREYAPDVPPPSPELEDRTIDALDGPHPIAVNRAKLRQLRPLWLVPVGIAAGLVVVWNGTRSPIPPQPSAEELAQLETYMETTWDGVLGETSLTESSDWFFPEASE
>NZ_CP051167.1|WP_168570251.1|4258171_4258723_-|periplasmic-heavy-metal-sensor
MKGRMHRRQLCALTALSVLLGTTAAYAAPPEFGNPEIVAQRPGGPGRGRGQGGQRWIEQLDLSQDQQQRIQQIRDRYRSEAESTYTQMMQLRQEMQDLMVGNGSDSQLRSKHDEMMKLHQRMGELRFDQMLEIRAVLSAEQRQQWAQQMQQRHQNRGNRQGNRPGNGRGMGPGGGMDDDFFGE
>NZ_CP051167.1|WP_168570250.1|4256313_4258047_-|ABC-transporter-ATP-binding-protein
MIRSSYGLLLPYLKPQWKTIAQALACTLGFTAFWPILARLAGDMAASIGAGDVATIAQLAGSAAVVFLVRGAVQYGQDALMAKAALAIALDLRQRVYAHLLHLSLGYFSHTQTGDLSYRLTEDIDRIGEVINKIFHQFVPCILQLIVVFSYMIYLNWQLTLASSIVAPLMALSIAWFGEKLRVFSHNSQSRIADLSAIVTEVFGGIRLVQAFCAEDYTLDRFRQAAERNRQARFSAEQLKAIQFPVVGFLEALSVLLLFFLGGWQIAQNNLTGSEFVSYVAAVALSIDPIAITTSNYNEFKQGEASVERVFELLSRQPEVTDKPGAIALPPVKGRIEYRDVTFSYHGKGPYPRPVLQEIDLTVSPGEAIALVGPSGAGKSTLVNLLPRFYDVQSGQVAIDGIDVKSVTLASLRRQIAIVPQETKLFTGTIAENIAFGQLDYDLDRVEAAAKIANAHEFITQMSEGYRSWVGEGGVNLSGGQRQRIAIARAVLLDPTILILDEATSALDSESEGAIQEALDRLMQGRTVLIIAHRLTTVRRCDRIVVLENGQILESGTHGELLAQEGRYAQFHAQQFY
>NZ_CP051167.1|WP_168570249.1|4254747_4256214_-|two-component-sensor-histidine-kinase
MTLIRRWIARPVHWLPKFDPHSLQIRLTVGMALVSALGIGTLAIATSWQMQRQLVATHKQTIKYIFDRFDRDVMHYSERNPAEKGLQPAIDSLSADRVLLWVKRPDGAIAAQSMPLSGRDDDTSKGLLGLPARQMMPQVSEIGGRFWVWCSGPLTVKGTHLGQLYIAADITEDRGILEGLIRTLALASGAAIVAMTVAIALYVRRSLRPVLEIGQLADRISVRELDTARIQLQNAPSEVRQLAQTCNTMLDRLAQSWEQQRQFVSNVSHELRTPLTLVSGYLQSTLRRATNLSEPQREALEIAASEAERTIQLLQDLLDLARADRGYLHFQLEPLLIVDLVAEVVEMAKQYSHREIAIVCGEDLLEASADRNRLKQVLLNLIDNAVKYSPSDTEIKVGVRSFGDRAIVEICDRGVGIPLAQQGRIFERFYRVDEARSRSVSPGESLATGGTGLGLSIVKTLVEGMGGTVTVRSKPGEGSTFGVILQRD
>NZ_CP051167.1|WP_168570259.1|4276312_4276627_+|nucleotidyltransferase-family-protein
MSITFRQSKIEIPEAAIAQICQDYHIRKLALFGSILRDDFRPDSDIDILVEFQPGKTPGFGFIDIQDCLSNLLGRTVDLNTPQDLSRYFRDRVVSEAEVIYGER
>NZ_CP051167.1|WP_168570260.1|4276891_4277326_-|hypothetical-protein
MPVCSYELDREVFRLLNSGIEGFDDWQNAARGIADYVASWGVERFWAMSRSQRLLGGQLPSEGVVSEEERRYFAWSVAREVLCKIVGTELGIDYEMNTDNFQEIFRELDFNQQVLLTDLLMEIAEAIQFWTMRLKDARESGTPA
>NZ_CP051167.1|WP_168570261.1|4277421_4278240_-|CRISPR-associated-protein
MRRSKTMAIEWLICREPVHIGGADSSSRGNNNPIYRLSDRTPTIPGSSLRGALREGAEHSSEYQGYVSNWFGGKDENISPGYIALGWGWPVWWPIHVLGYGSWWVSCPAWLNRYQQLSQQNLLNLTEGNIYATDPQFNNQTVYLRWLKLTQIQTCTLSLPAPSEVPPDRRIIVPSDSINLIVDMGLVRQPRVSLNEEPDKKGSLVKNLFAVEGLPPGAVFMTSWTIRNPEKVEQIGEWEKFLRSEHYLGGLWSVGYGRIAIAQTADSTLSQE
>NZ_CP051167.1|WP_168570262.1|4278211_4279255_-|hypothetical-protein
MSELEQSWYSISPAGTVAIGNLTPVGQNSGQVDCRWPPNGHQLAACLNLPTDCTLCGPFWYLSNPGRIYVILPLPVYELERSPQKKKKQKIPPEIFRMVWEENRWQVQSQHRDASIEVVGGRYLISGITLKQLWRDGSRKEPDLQEFPWQKLTLSHNSREEFEVKDEGGFFAEKTTLMDPGWSILVKIIGNYDWQQRLPNPPWSCIGAGATPVSIKREDEEDLTVDWLEGKAESFQGTGAVLLTGALWYEEENFLSVPYPAQVPIAGYAAEVGIPWQSWKSVRDRHNPERKVQVLTPGEWLTPAGAVYLWEGEAPLETSAPLPDRHHRHCLGYGHLWLFEEKQNNGN
>NZ_CP051167.1|WP_168571943.1|4279251_4281507_-|hypothetical-protein
MAIEDWLIQQQQIYQNLPDASPEISIHPVSGEWQTSAYLKSQFWWGGGASIEACRQVAAASNPELTHLGVLSFGPVQEFLGGGERLRDWAVASWLCHYLTAVAIYRWEERQGQVLLPLHRSSPLLNWLRDEPCDRDRFWQAELPNVITGLHPQDETWLQDFNPIITQEWGKFLEALEEEVSQRYSPHLLNGQGWQVIHRDNAYLWSVYTESTPLSLATVSQDIKQLRERIESRKIGRQWQATWWGGRTSPSAGHLSIWHPGLKPIHDGGTWGLPDSQLKEWWLRAANESRDRLSGLVDSDDRLNSIEFVRRLASVPDIIEPTLQLLWGRTPPPCPWGQFPDRATVAAAWVVDRIDAETWNDTLDTLYQCCLDEKPNFRWGMPKVDGKNPPHFAYPRILERRYLKERVPQEKKDTDDEKKIIKDWEDLSQGWESPIEWTVGWRGDGDNMGKWLSGKQYETLKLQWSRWHLNQDAILQHQLNIDPPTLSANATRKLDLPHVLDLSVLFGCWNQLLYPLTERHHNAKVIFAGGDDFLLLGPLTEAVSLTSNLYRLWRGQLSPLTQPLDPPVDGWVKRESEIYPVPGQRMDFSLGVAIAQRRIPQSLWHRGLTEAYKEAKNQGRDRVCIKVLFNSGQSLDWVCPWRLWELLMHVGLTTEEKTELNRWEKLLSYLESNRLQQSDVDTVRDLIETLWASVGIALTWEAIETVAEYDEFDDELGNWSWWIGWISVMGFLARQQREREKWVERVGGNNP
>NZ_CP051167.1|WP_168571816.1|4281508_4282546_-|IS630-family-transposase
MNIIDELDNFIENTTNTKEMKRALAAKMKLSGQPSKKIEEILNVSSSFVSQWKNKAIFEGVESLNLQYKGSKGYLKPEEKTQITSWIRQQEYLRLSDLKRYLQQEYNVIYSSNQSYYDLLKAAGMSWKKSQKKNPAKDEKLVKKKEEEIQKKLKDWEEDIKAGKLAVFMIDECHLLWGDVLGFVWGRKDIRVEIPIKNQKSRQSYYGALDYQTHEFILQEYPKADTDNTIQFIQYLREQRPGQKLAIFWDGARYHDSQQFRDFLKELNEGLEEDEWLITCTKFAPNAPEQNPVEDIWLQTKNFLRTFYFLCDSFKRVKELFKIFADGQVFDFPKLYSYGFLPQMT
>NZ_CP051167.1|WP_168570263.1|4282631_4284095_-|hypothetical-protein
MTTLILQVLGNSDITSGDLKGWETLTESDSLKGIERRAGINSKKFCEGKTDFDFPLIRKLITATEGVNSSTALFCFILTDQTDWQSQRSETGQGWANIVAKDGIWWKEILAKWCDKNNIKQYSVRFKIEPNLLNGTADWEGMAEKIEKLFKILINFEGDYIYFQPTKEESILIDKIIVQHSSGTPALNGALYLWGIERKLTVKSIDFVYISEEQLECEPHSGTHWQWHLKVPQIRELLKIQDFSGALQILKSHPHSIEEIKTKLQELDRAVSLNLTGRENLTGREGIIERVAIAVWSETAFRDRSQWMHWYLRVAGAFELAILLLIEKQGNGDYEWQGIKLLDPDQKDISPCSIAAIVYPLLTKGVWEYISPKKEIHQFTIAPVTDCNWVKFKKFYVDIWELESKPKTTQAFTSIRNKLYHSLLGDRIDELLDKKTEELGSVTHEKHPAQVAVDYLHYIIDLAGLTDEVQERATTYREIVENIEENL
>NZ_CP051167.1|WP_168570264.1|4284162_4286073_-|hypothetical-protein
MILFNGGVGFLRVQVQPIGNILLDWLDFLHFFRFLVPRQGTEVKAYKRTDKGDEDYFPEKLGNGNGDRSVFKAVVMALLQTVSREIWWDDIFVPDRLIPFVCLYVNDLPQSEINQFHLLYKLQHFFNSNQGEYPAPEHLDPNPQPWLAYARNHWFIFTLEGGTFLAIDSPEEVFFKETLPQHVKSQYFLLFLLAQYQRFALMSLSQQVANFWLAAEEQRLQEFERIRDRLFLFTARGYFTQVMQRDNYHRCYRKWQEVLQLEQLYREVHDEVHEMQEYLNSQSLRRLEVAEKQRERERQEEKERQEKLEKQREQQYLQELRSKDEAQAKRDRELQDLAYIISGGLGGAAIFASSAGLLTAGSNNGEVTVGWIPTPFNTLHPVTVAIFLSFLAALLFGFTVWGVREGRRWVCDRRAQRKLEAFCLLLERDPAWLSWGDREWLSWGDREQLAELIDCEPNDPRELWEAIARWCQSQSDPRVVRKLAILEKRVKLHAKVHKNYKAELRAKISPPTAAQKTIEGFLQLLHNQPDLFDLEARNDLARQNWSAEPEKLAEQIRKWCQIDRRSAIYAQLLEEQNNWPPHLPISTGNEYSDRLKEASCRLQRLAKPPSLFKKLLNESLRDLEQGWQRIMRSPPP
>NZ_CP051167.1|WP_168570265.1|4287178_4288261_+|tetratricopeptide-repeat-protein
MFKSLRGKKFDRAWIVLACNLSIALMTPAAIAQSLESLFQEGSAAFNTRDYTRSEQIWRAVLERDRDNAAAYDWLGLSLYYQDRVEEAIAAYRQAIALDPQQSSAYNNLGNALNDRGQFEEAIAAYRQGLDINPNQGQTHYNLAVVLSATGRIPEAIASYRRAIQLNPTDGEAYLKLAGLLRRSDRPDEAIVAYRQALQVNPNQARAYNELGIVLVRQGNLEEAIAAYERALQIEPNWAAVHNNLAVALQRQDRPDEAIAAYRRALELDPNLATAYNGLGVIYRQQGQFDESIAHFERAIALPDRAAIPANSRVLAYNGLGLTLQAQGKIAEAIAQFERAVELDPSYTPAQYNLKQIRGQ
>NZ_CP051167.1|WP_168570266.1|4288325_4289819_-|glycosyltransferase-family-2-protein
MKFTIAIATYNRLPLLKRAIDSALAQTLSCEVVVVDDASTDGTEQYVRSLSEALRAAGDKRLVYCRNKENSGHALTVNKGVEVASGDWVKLLDDDDYLAFNCIEEMTRAIALHPAAAICSCQASQVDENECELSRTREVGPGRAFYIPQEDIHYGMLLELVPFGTPAQVAFRRDAFLETGGWDSSLDTNCDDIDSWIRIAEHGDAIFINQCLAFRTVWGEAYNKKITIQKRLETNILMKQKICDRISEKHRDRVPAFQNITAYLKLHWLFVALKSKQLPTALKLAFPSIFRYRGWKLLLETILSRKFNNFSSLNLITEKTLKSVQISSSASPVNPPTFGGSNPELIREQLRLKASKMAFKKGNPIAGVKLGFPALVSMVNRKLFGKTQNLSQTGNRSEIQASGDRNAENNVVVIDRIETLIKNKQNVDLSEIKQVRDYFKLRWSWLALKHGKVAEAVKIALPALFSLNAWKLFIQALLKDKQEKNKSLVQKIVLIDY

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Crispr_ID: NZ_CP051167_22

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_22

4379530-4380495

TypeV

N:A

Consensus_repeat	Method
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	CRISPRCasFinder
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	CRT
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	PILER-CR

12 spacers

cas14j,cas2,cas1,csx18

The CRISPR arrays of NZ_CP051167_22

>merge|NZ_CP051167|22|4379530-4380495|CRISPRCasFinder,CRT,PILER-CR
CCCTACCGAAACTTGCGGGGAGTTGGGCATAAGTGACCCCTCTTCGACGATAAACTGTCTACCTTGTGTCTTGAGTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGACGGTGATGGAGGAGGTGGTCAACTGAACCTCTACGCGGAGTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGACTGGAAGCTTAAAGCTAAGGAAGTGGCAAAAGGTTACGATGAATTGTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGACGGCTTGTACTTCTCGACAAGTAACCCCTGTGCGCGTCGTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGACAAGTCGGCGTGGTAAGAACCGGGCTGACTATCGTAACCGTGAGGGTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGACGCCTTATCGGTAAAGCTGAGAGTGCGACCCAAGCACGGGTTGTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGACCTTGAGGTCAAGTTGTACCCCACCCCTTGTGGTGGCTACAGTTTGGCTGTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGACCCGTATATCCGAAGGATTCTCTCTAGTAAAGGCGAGAACAGTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGACCAGTGAAAGGGTTCGCGCGGCGGACTGGAGAGATATTTAGTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGACTGGTAGAGATGGAAGATTTAGTCGTCCTCAGTAACGGGTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGACTGGAGACCAATGGGATAACGTTATTCCGACGGTGGACGGGTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGACTTCCTCTGCTCAAGCTCCGGTCATTCGTGTACCTGCTGAGAGTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC

>NZ_CP051167|22|20|4379530-4380495|CRISPRCasFinder
CCCTACCGAAACTTGCGGGGAGTTGGGCATAAGTGAC	CCCTCTTCGACGATAAACTGTCTACCTTGTGTCTTGA
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	GGTGATGGAGGAGGTGGTCAACTGAACCTCTACGCGGA
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	TGGAAGCTTAAAGCTAAGGAAGTGGCAAAAGGTTACGATGAATT
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	GGCTTGTACTTCTCGACAAGTAACCCCTGTGCGCGTC
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	AAGTCGGCGTGGTAAGAACCGGGCTGACTATCGTAACCGTGAGG
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	GCCTTATCGGTAAAGCTGAGAGTGCGACCCAAGCACGGGTT
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	CTTGAGGTCAAGTTGTACCCCACCCCTTGTGGTGGCTACAGTTTGGCT
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	CCGTATATCCGAAGGATTCTCTCTAGTAAAGGCGAGAACA
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	CAGTGAAAGGGTTCGCGCGGCGGACTGGAGAGATATTTA
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	TGGTAGAGATGGAAGATTTAGTCGTCCTCAGTAACGG
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	TGGAGACCAATGGGATAACGTTATTCCGACGGTGGACGG
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	TTCCTCTGCTCAAGCTCCGGTCATTCGTGTACCTGCTGAGA
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC

>NZ_CP051167|22|11|4379530-4380495|CRT
CCCTACCGAAACTTGCGGGGAGTTGGGCATAAGTGAC	CCCTCTTCGACGATAAACTGTCTACCTTGTGTCTTGA
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	GGTGATGGAGGAGGTGGTCAACTGAACCTCTACGCGGA
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	TGGAAGCTTAAAGCTAAGGAAGTGGCAAAAGGTTACGATGAATT
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	GGCTTGTACTTCTCGACAAGTAACCCCTGTGCGCGTC
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	AAGTCGGCGTGGTAAGAACCGGGCTGACTATCGTAACCGTGAGG
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	GCCTTATCGGTAAAGCTGAGAGTGCGACCCAAGCACGGGTT
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	CTTGAGGTCAAGTTGTACCCCACCCCTTGTGGTGGCTACAGTTTGGCT
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	CCGTATATCCGAAGGATTCTCTCTAGTAAAGGCGAGAACA
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	CAGTGAAAGGGTTCGCGCGGCGGACTGGAGAGATATTTA
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	TGGTAGAGATGGAAGATTTAGTCGTCCTCAGTAACGG
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	TGGAGACCAATGGGATAACGTTATTCCGACGGTGGACGG
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	TTCCTCTGCTCAAGCTCCGGTCATTCGTGTACCTGCTGAGA
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC

>NZ_CP051167|22|18|4379604-4380495|PILER-CR
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	GGTGATGGAGGAGGTGGTCAACTGAACCTCTACGCGGA
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	TGGAAGCTTAAAGCTAAGGAAGTGGCAAAAGGTTACGATGAATT
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	GGCTTGTACTTCTCGACAAGTAACCCCTGTGCGCGTC
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	AAGTCGGCGTGGTAAGAACCGGGCTGACTATCGTAACCGTGAGG
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	GCCTTATCGGTAAAGCTGAGAGTGCGACCCAAGCACGGGTT
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	CTTGAGGTCAAGTTGTACCCCACCCCTTGTGGTGGCTACAGTTTGGCT
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	CCGTATATCCGAAGGATTCTCTCTAGTAAAGGCGAGAACA
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	CAGTGAAAGGGTTCGCGCGGCGGACTGGAGAGATATTTA
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	TGGTAGAGATGGAAGATTTAGTCGTCCTCAGTAACGG
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	TGGAGACCAATGGGATAACGTTATTCCGACGGTGGACGG
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC	TTCCTCTGCTCAAGCTCCGGTCATTCGTGTACCTGCTGAGA
GTTTCAATCCCCTTGCGGGGAGTTGGGCATAAGTGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168570330.1\|4382752_4383364_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP051167.1\|WP_168570326.1\|4374928_4375129_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570323.1\|4372859_4373159_+\|DUF3007-family-protein	unknown	unknown	gnl\|CDD\|371542
NZ_CP051167.1\|WP_168570329.1\|4382317_4382641_+\|hypothetical-protein	csx18	cls000006_csx18_CAS-I:CAS-III	unknown
NZ_CP051167.1\|WP_168570327.1\|4380826_4381111_-\|CRISPR-associated-endonuclease-Cas2	cas2	COG1343_cas2_CAS-I:CAS-II:CAS-III	gnl\|CDD\|273699
NZ_CP051167.1\|WP_168570325.1\|4374311_4374656_-\|DUF760-domain-containing-protein	unknown	unknown	gnl\|CDD\|368489
NZ_CP051167.1\|WP_168570332.1\|4387425_4387596_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570321.1\|4371399_4372392_+\|photosystem-reaction-center-subunit-H	unknown	unknown	gnl\|CDD\|224785
NZ_CP051167.1\|WP_168570324.1\|4373403_4374198_+\|tryptophan-synthase-subunit-alpha	unknown	unknown	gnl\|CDD\|237285
NZ_CP051167.1\|WP_168571950.1\|4370055_4371312_+\|transposase	cas14j	-	gnl\|CDD\|223747
NZ_CP051167.1\|WP_168570322.1\|4372527_4372764_+\|NAD(P)H-quinone-oxidoreductase-subunit-L	unknown	unknown	gnl\|CDD\|313841
NZ_CP051167.1\|WP_168570333.1\|4387582_4388056_-\|peptide-methionine-(S)-S-oxide-reductase-MsrA	unknown	unknown	gnl\|CDD\|376578
NZ_CP051167.1\|WP_168570319.1\|4363773_4365702_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|99707
NZ_CP051167.1\|WP_168570328.1\|4381201_4382212_-\|CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|376633
NZ_CP051167.1\|WP_168570335.1\|4390471_4392781_-\|response-regulator	unknown	unknown	gnl\|CDD\|223715
NZ_CP051167.1\|WP_168570318.1\|4363213_4363435_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570331.1\|4383401_4387265_-\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|238923
NZ_CP051167.1\|WP_168570320.1\|4366147_4369873_+\|chromosome-segregation-protein-SMC	unknown	unknown	gnl\|CDD\|274009
NZ_CP051167.1\|WP_168570334.1\|4388842_4390090_+\|WD40-repeat-domain-containing-protein	unknown	unknown	gnl\|CDD\|238121
NZ_CP051167.1\|WP_168570336.1\|4393057_4399591_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|236848

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168570330.1\|4382752_4383364_+\|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.	2.57582e-16
NZ_CP051167.1\|WP_168570323.1\|4372859_4373159_+\|DUF3007-family-protein	gnl\|CDD\|371542	pfam11460, DUF3007, Protein of unknown function (DUF3007). This is a family of uncharacterized proteins found in bacteria and eukaryotes.	2.57852e-53
NZ_CP051167.1\|WP_168570327.1\|4380826_4381111_-\|CRISPR-associated-endonuclease-Cas2	gnl\|CDD\|273699	TIGR01573, cas2, CRISPR-associated endonuclease Cas2. This model describes most members of the family of Cas2, one of the first four protein families found to mark prokaryotic genomes that contain multiple CRISPR elements. CRISPR systems protect against invasive nucleic acid sequences, including phage. Cas2 proteins have been characterized as either endoribonuclease (for ssRNA) or endodeoxyribonuclease (for dsDNA), depending on the system to which the Cas2 belongs. CRISPR is an acronym for Clustered Regularly Interspaced Short Palindromic Repeats. The cas genes usually are found near the repeats. A distinct branch of the Cas2 family shows a very low level of sequence identity and is modeled by TIGR01873 instead of by this model (TIGR01573).	3.04868e-22
NZ_CP051167.1\|WP_168570319.1\|4363773_4365702_-\|AAA-family-ATPase	gnl\|CDD\|99707	cd00009, AAA, The AAA+ (ATPases Associated with a wide variety of cellular Activities) superfamily represents an ancient group of ATPases belonging to the ASCE (for additional strand, catalytic E) division of the P-loop NTPase fold. The ASCE division also includes ABC, RecA-like, VirD4-like, PilT-like, and SF1/2 helicases. Members of the AAA+ ATPases function as molecular chaperons, ATPase subunits of proteases, helicases, or nucleic-acid stimulated ATPases. The AAA+ proteins contain several distinct features in addition to the conserved alpha-beta-alpha core domain structure and the Walker A and B motifs of the P-loop NTPases.	0.00250354
NZ_CP051167.1\|WP_168570321.1\|4371399_4372392_+\|photosystem-reaction-center-subunit-H	gnl\|CDD\|224785	COG1873, COG1873, Protein implicated in RNA metabolism, contains PRC-barrel domain [General function prediction only].	0.000276124
NZ_CP051167.1\|WP_168570324.1\|4373403_4374198_+\|tryptophan-synthase-subunit-alpha	gnl\|CDD\|237285	PRK13111, trpA, tryptophan synthase subunit alpha; Provisional.	5.05054e-133
NZ_CP051167.1\|WP_168571950.1\|4370055_4371312_+\|transposase	gnl\|CDD\|223747	COG0675, COG0675, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	2.19711e-39
NZ_CP051167.1\|WP_168570322.1\|4372527_4372764_+\|NAD(P)H-quinone-oxidoreductase-subunit-L	gnl\|CDD\|313841	pfam10716, NdhL, NADH dehydrogenase transmembrane subunit. The NdhL family is a component of the NDH-1L complex that is one of the proton-pumping NADH:ubiquinone oxidoreductases that catalyze the electron transfer from NADH to ubiquinone linked with proton translocation across the membrane. NDH-1L is essential for photoheterotrophic cell growth. NdhL appears to contain two transmembrane helices and it is necessary for the functioning of though not the correct assembly of the NDH-1 complex in Synechocystis 6803. The conservation between cyanobacteria and green plants suggests that chloroplast NDH-1 complexes contain related subunits.	3.73734e-24
NZ_CP051167.1\|WP_168570333.1\|4387582_4388056_-\|peptide-methionine-(S)-S-oxide-reductase-MsrA	gnl\|CDD\|376578	pfam01625, PMSR, Peptide methionine sulfoxide reductase. This enzyme repairs damaged proteins. Methionine sulfoxide in proteins is reduced to methionine.	2.74173e-89
NZ_CP051167.1\|WP_168570325.1\|4374311_4374656_-\|DUF760-domain-containing-protein	gnl\|CDD\|368489	pfam05542, DUF760, Protein of unknown function (DUF760). This family contains several uncharacterized plant proteins.	2.02357e-36
NZ_CP051167.1\|WP_168570328.1\|4381201_4382212_-\|CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|376633	pfam01867, Cas_Cas1, CRISPR associated protein Cas1. Clustered regularly interspaced short palindromic repeats (CRISPRs) are a family of DNA direct repeats found in many prokaryotic genomes. This family of proteins corresponds to Cas1, a CRISPR-associated protein. Cas1 may be involved in linking DNA segments to CRISPR.	3.01215e-103
NZ_CP051167.1\|WP_168570335.1\|4390471_4392781_-\|response-regulator	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	2.39013e-49
NZ_CP051167.1\|WP_168570334.1\|4388842_4390090_+\|WD40-repeat-domain-containing-protein	gnl\|CDD\|238121	cd00200, WD40, WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from its N-terminus and the WD dipeptide at its C-terminus and is 40 residues long, hence the name WD40; between GH and WD lies a conserved core; serves as a stable propeller-like platform to which proteins can bind either stably or reversibly; forms a propeller-like structure with several blades where each blade is composed of a four-stranded anti-parallel b-sheet; instances with few detectable copies are hypothesized to form larger structures by dimerization; each WD40 sequence repeat forms the first three strands of one blade and the last strand in the next blade; the last C-terminal WD40 repeat completes the blade structure of the first WD40 repeat to create the closed ring propeller-structure; residues on the top and bottom surface of the propeller are proposed to coordinate interactions with other proteins and/or small ligands; 7 copies of the repeat are present in this alignment.	9.00538e-94
NZ_CP051167.1\|WP_168570331.1\|4383401_4387265_-\|diguanylate-cyclase	gnl\|CDD\|238923	cd01948, EAL, EAL domain. This domain is found in diverse bacterial signaling proteins. It is called EAL after its conserved residues and is also known as domain of unknown function 2 (DUF2). The EAL domain has been shown to stimulate degradation of a second messenger, cyclic di-GMP, and is a good candidate for a diguanylate phosphodiesterase function. Together with the GGDEF domain, EAL might be involved in regulating cell surface adhesiveness in bacteria.	1.2824e-107
NZ_CP051167.1\|WP_168570320.1\|4366147_4369873_+\|chromosome-segregation-protein-SMC	gnl\|CDD\|274009	TIGR02169, chromosome_segregation_protein_related_ptotein, chromosome segregation protein SMC, primarily archaeal type. SMC (structural maintenance of chromosomes) proteins bind DNA and act in organizing and segregating chromosomes for partition. SMC proteins are found in bacteria, archaea, and eukaryotes. It is found in a single copy and is homodimeric in prokaryotes, but six paralogs (excluded from this family) are found in eukarotes, where SMC proteins are heterodimeric. This family represents the SMC protein of archaea and a few bacteria (Aquifex, Synechocystis, etc); the SMC of other bacteria is described by TIGR02168. The N- and C-terminal domains of this protein are well conserved, but the central hinge region is skewed in composition and highly divergent. [Cellular processes, Cell division, DNA metabolism, Chromosome-associated proteins].	0
NZ_CP051167.1\|WP_168570336.1\|4393057_4399591_-\|PAS-domain-S-box-protein	gnl\|CDD\|236848	PRK11107, PRK11107, hybrid sensory histidine kinase BarA; Provisional.	7.32798e-127

>NZ_CP051167.1|WP_168570326.1|4374928_4375129_-|hypothetical-protein
MGDRPGKVNHFLGGVTGRAIAPAFVKIWQRFGEFCQDRAAPWRRSPGRALPFLILDCPFPPPTEGA
>NZ_CP051167.1|WP_168570325.1|4374311_4374656_-|DUF760-domain-containing-protein
MVYQPDFMYSNSEDEQVNPLLRYLQDQPPEVLARVAKTVSPEIKEIISQNVQGLVGVLPSENFDVQITTNRENLAGLLASAMMTGYFLHKMEQRMHLDENLGGIGSIASDSAED
>NZ_CP051167.1|WP_168570324.1|4373403_4374198_+|tryptophan-synthase-subunit-alpha
MKSVSQCFESLRQQQQCALIPFITAGDPDLETTAKALKLLDDKGADAIELGVPYSDPLADGPVIQAAATRALRRGTRLEQVLAMLERVTPTLRAPIILFTYYNPILYRGIESFLKSAAQAGVKGLVVPDLPLEESDEVLSRAAECGIEVILLVAPTSSADRIEAIAHQSQGFIYLVSVTGVTGMREQVQARVPDLLDRIRSYTDKPIGVGFGISAPEQARQVKEWGADAVIVGSAFVKRLDDPSPEAGLAAVGEFCASLKAAIA
>NZ_CP051167.1|WP_168570323.1|4372859_4373159_+|DUF3007-family-protein
MRRIDAIGIGLGIFIAGGLAYTLLQGAGFDATSAGIWSQLLLVGGLLGWLASYLWRAVSGNMTYHQQVKDYEEAVLNKRLEEMSPEELERLQAEIEAQE
>NZ_CP051167.1|WP_168570322.1|4372527_4372764_+|NAD(P)H-quinone-oxidoreductase-subunit-L
MRQMLDSTLFVLLLYAGLGGAYLLVIPGLTYFYLQRRWYVVSSVERVFMYLLVFLFFPGMLLLSPFLNFRPKRREIGA
>NZ_CP051167.1|WP_168570321.1|4371399_4372392_+|photosystem-reaction-center-subunit-H
MTSDKIRQRSDLLNTQVITRNTGKRLGVVKELLVDIDRREVVALGLRDNLLAIAGMPRFMLLDSIQQIGDVILVEDENVIEDVDVESYSSLINSEVITENGELLGKVRGFKFNVETGEVVSIVIAALGLPQIPDQAISTYELPVEEVVSSGPNRLIVFEGAEDRITQLTVGVLERLGIGEPPWAREAEDEYLMPTASPENRLGTGARTPAPEPVRSPARVVEEVWDEDQAWEQPAPEPLRQPEPEPIYYEDEVAEENWSEATKDDRYYDEPYGEPVYGEAYEEVEYDEDYDEDVEGDAWADEGADKPYTPPRVNIPEKTKTTQYEEEPGY
>NZ_CP051167.1|WP_168571950.1|4370055_4371312_+|transposase
MNYTYRIYPNVVQQTELLSWLETCRGVYNYALRELKDWIASRKCSVDRCSLEKEYIIPADEPFPSYHRQQNNLPKAKKQFPHLGKVHSQVLQNTIRRLHDTWEAFKKRGHGFPRFKKFGQFKSFLFPQFKHNPINGFTIKLPKLGEIPMNLHRPIPDGFKVKQVRVLSRVRGTQWYVVVTIESDISVPDVPVHGRAIGIDLGLQRFLTASDGSFQERPKFFKSMQRKLKLLQRRAARKQKGSQNWEKAQIEVARMHHRIANRRKDFHLKTAHQLCDRAQTIFAEDLNVTGLTRGMLRKDCVDAAFGQFLSLTEWVCWKRGVYFAKVNPNGTSQTCPSCLATVSKGLEVREHHCPECGYRTHRDHAAAEMVLDRGLENVVAQGLWGTETACQVGLSGVYDLDKWRGAGIPNREAGKPAL
>NZ_CP051167.1|WP_168570320.1|4366147_4369873_+|chromosome-segregation-protein-SMC
MVHINRLELTNFKSFGGTTSIPVLPGFTVVTGPNGSGKSNILDALLFCLGISTSKGMRAERLPDLVNHNLARSRTTVEASVTVTFDLEGEGLPTEEDYLQEAQAIADPGPAQVQPSEEPQEQNGTLASPGNEAAIAESDPQAVRESDPSNEWSITRRLRVTKAGTYTSTYYINGQACTLSELHEQMNRMRIYPEGYNVVLQGDVTAIISMNARERRTIIDELAGVAAFDRKIAQAKDKLDEVKEREDRCRIVEQELISQRDRLAKDRDKAQKYQALRAQVQEKELLEAVLQWHQLNQQEWKLREQIEAGDREAAQLRDRVATASGEIQQANERLEELNARVKALGEEELLAKQSVLAQREAEKEQQGQRLHELQESQQQQQRDIAEAEREIGHYQQKLEQVAQERQESDAQLKSARQLSDELQQDLDRRRERASAIAAASEEWVQQQTALHRQIETLQKSLDPQRTEQARLGERVRSLDRAIAEQHETLQDFGARLAEKKVNLGEVDLRHQAAIDRVQSLAGGLAAAENDLKTQQDTEKRLLDEQREKQRRLDKLEAQTQALREASGTGASQVIVQAGLQGVCGLVAELGRVDPHYQLALETAAGGRLAYLVVEDDAVAASAIQLLKQKRAGRATFLPLNKIRPPRFSPIAELRQARGFVDYAVNLIECDRPYLQVFAYVFGNTVVFETLDAARSHMGKTRIVTLDGELLETSGAMTGGSSSHRSSLHFGTGGDTESAEVTELKERLEQIEQILQRCGEAIAQAAEQVKGRSQELIDAKQQQRELQLKTEQLQGEIDSLSAQQQQVRQQLADNTQELTAARDRLQVLDGEIPSQEARLQQWRHELSALEESGTNSEWQGIQAQVRQLESELQDASASLRAAQSRRQDLDNQQQRLDEKRQETRRRLEDLNHAQINLDSRIEQTRAKLGEIDENIAQNRRELAEIEAKLGEDKQARDRAEEALRQLHLARQQIEWQGQKLQESQDARREQLGALREQIAAGRAELPDPVPPVPEESKNRLVTALQELQKEVRSLQKQLKAMEPVNMLALEEYDRTQTRLEELQSKLATLEGERTELLLRIENFTTLRLRAFKEAFDAVNENFQTIFADLSEGDGYLQLDDPEDPFSSGLNLVAHPKGKPVQRLAAMSGGEKSMTALSFIFALQRYRPSPFYAFDEVDMFLDGANVERLAKMIKQQVQRAQFIVVSHKTPMIKAAERVIGVTQARGAHTQVVGLNLESNSAPV
>NZ_CP051167.1|WP_168570319.1|4363773_4365702_-|AAA-family-ATPase
MSCTSVSSAIVHLNAAIAAANPFERATRVTEREIWWATPPNLEGLNPEAIAAVLDAVERARKRIEPLSSLAILGETGTGKTHAIACVRQQLQRDRRGLLVYVNAGQFSDVNLIRYQFLQTVVDSFRHPGSANFMQWQDLATAIALEAFQSIYPERDRFSVDSLVNKLNRQTLSKNQTWIAQLSEAFFKIRPTLGDPDLVRALLWTLCHAQAPYAIKWLAGQVLASAKAEELGLPNRSRDYRDAQGWEIVLEIFSLATQFYPVVIAFDQLDSPENSDTGLKRERVVASLVKRIWETLPIARLNYGVVLAIAATPQTWYEKIQSLPSGIVAYLSKSVAPIRLQAIDVRGMRELVGLFLQQFYDRCHLIPPRSLYPFDSDQLDALAREELNVRELLEWCAENFRPVEVDPWEAVQIALDRAKQTVEERQLHADRRSLVAALQLALQMLLDRSIAGVTLEAVESMEARDLHDRRYVPLRAIVRTDAGSHAIGLAIVPRLNASELRATFARLLDRDRLGLDGACLLAPQIPAHWQCRQGLARFIRGDRCSYIPLDRDALTPLLALWWLHRERQQWQLGDREIVEFVRQHQFLAENPTISAILSTAIAPLPQAVEGDGDRPYFPPDRRSNPTGNDRNLLKIDESNDSP
>NZ_CP051167.1|WP_168570318.1|4363213_4363435_-|hypothetical-protein
MCMSLAISLIFALVAGSICLGTRDEMIAILSGTIAAVSSVVVIFLVAWQIQLLLVCLLVGLSKVFAVEDATHA
>NZ_CP051167.1|WP_168570327.1|4380826_4381111_-|CRISPR-associated-endonuclease-Cas2
MTDFWLVCYDVRDDKRRNKLAKLIEQRCQRVQYSVFECPVEGEILCELIERRWLKVLKLSEDSLRAYPLSGTAKKQAKIYGSPPLYEPPDYLIL
>NZ_CP051167.1|WP_168570328.1|4381201_4382212_-|CRISPR-associated-endonuclease-Cas1
MTTLYLTEPGTYVRYRNHTLDIKKEDRHHTCRLSELDLVVVLPGVQLTDGAIAQLLDRGIETLFLRQDGRFRGRLQGHFHSNPSIRLAQYRCVETTFGLALAQKLVSGKIRNQRTLLQQRNRATQGRIGELSEAIDAIASYSSRLQQLATPLTRDELMGIEGICAKNYYQALRHWFPTQWNFSGRNRRPPLDPINALLSWGYGVLLARVFAAAVQAGLDPYLGFFHAIEPYRPNLVLDLMEEFRPVIVDRAAIAIVKAELLDPLDFEPSPDGAGIWLGQTAKKLFLGQLQRQFSSRVLYSPQNRRLTLAQILLEQARSLGRCLCESNLDYEPFLLK
>NZ_CP051167.1|WP_168570329.1|4382317_4382641_+|hypothetical-protein
MSKVMTRQLVRYRSIFVAIANAAVTWVILIIAPLGLFSVITCTALVFVASLLNGWMGDRALLSLLAASDRDAVVSTSQGTPLSAPDSPSVGDRAIGEPERNKELPRE
>NZ_CP051167.1|WP_168570330.1|4382752_4383364_+|tetratricopeptide-repeat-protein
MELIILLVILVWIAVETGIWERFWQNKRLLRQQTREEAVFQELVKQLERENGDRTNATHLEGVGTFKIAAGNYREGIADLTRAIALNPAKASLYCNRAQAFYLLEDWGQAVRDYRKTIELDAEEIGAYIGLARVFLQIGDYREAIATCNGAVLLDENEAIVYTLRARAYRRLGDRDRARRDCDRAEICDPNHVEVQHLRTELN
>NZ_CP051167.1|WP_168570331.1|4383401_4387265_-|diguanylate-cyclase
MFKPLRLQEQLLYQIVNCIHDSFDLQEILAGIVSQIREFLAVDRVKIYQFAADGSGEVIAEAIGGDRLPSLLGLHFPATDIPAYARDRFAKGHLRTIVDVASKRKILNRLGPQESDGETAGPNYAPVDPCHLQYLLAMGVLSSLAVPIFDRGATPEGYRAQLWGLLVAHHSEPRRYSETELQTIDLLAHQISIAIAQTSLIAKAQEQVRQEQIVARLSRQLDGGGDRDRLWQTALNECVTALNADGGRLYVGADLTGEPSQCFICGEQPAREDLESYALWQQLTKYGGSKSRDRQDPAAAIADPPQGAFPYTVAQLDADPHWQDLAALFAPTPIQSLLIVPLRYCNQWVGSLVLFRHARDIEKRWAGRHNSDPRNQMPRQSFAEWCAIERLTPNWSPEDLQLAQRLGLHLYAALTQHRVTRLTHSQASYDTLTQLPNSVLFERQLSLALLHLREQGEMLAVAILDLDRFQTINETFSHAGGDYVLTDVTRRLQRCLETYRDRFQDRGSLLGRWHGDEFVLMLPNITYAEDIIDIGRELLDSLQQPFYFQGRELYLSACLGIALAPYDGETAPILLKHAEAAMYQAKQQGQNSYQLYAPQMNTRDLERLMLEVDLRKALERDEFVLYYQPQVELGTGRIVGMEALLRWQHPRLGFVPPEQFIPLAEELGQIAAIGEWVLYKACTQHRAWQLAGLPSVRMAVNLSARQFREENLVEKVREILLQTQVDPQLLELEITENTAIDDLEFTIAVLQQFKQVGIRVAIDDFGMGYSSLSALKHLPIDSVKIDKSFVRDLGMEESDTAIVRAIVALGRGLHLETIAEGVESWPQLEVLQSVGCDRVQGYLIGEPLAADAAVAMLVAGRLSCLRKSESAVTAVAATLTQQAHHRSQETDNRPVATLDSGNGAVADGSGDDRPSPETQENRQELAAKIVEYEQLKEELKQQARREQLVGEIAQKIRRSLTLSEILNKTVTEVRHFLQADRTILYRFHPNWTGEVVVESVAPGCLSILGETIDDPCFRNNYVKYYRQGRIRAIENIFEAGLNSCHLQLLDRYRVKANLVVPVVNGDTLWGLLIAHQCHDTRQWRQHEISLLSQLATQVAIAIHQGELYSQLESTNRELQELSSRDGLTQIANRRLFDLHLEREWQRLKREQAPLALVLCDVDRFKLYNDTYGHQAGDICLQEVARGLQGAVKRPADLVARYGGEEFAAILPNTPASGALRVAEEMRMRVRDLQIPHSKSEHHRVTLSLGVAVLVPTAGLSPEALIQAADEALYRAKEHGRDRCTLAT
>NZ_CP051167.1|WP_168570332.1|4387425_4387596_+|hypothetical-protein
MLSRSPPIATDRPRQPTGIARARAIHSEKRLKNECEGLIEGAIPQKSSTAIGSNFD
>NZ_CP051167.1|WP_168570333.1|4387582_4388056_-|peptide-methionine-(S)-S-oxide-reductase-MsrA
MVLEKATFAAGCFWGVERRFRQVPGVVSTSVGYTGGHFPNPCYLDVCARITGHAEAVQIEYDRDRLSYEDLLEVFWTCHDPTQVDRQGPDRGEQYRSVIFYHDSQQERAARRSKLTWERSGKFEKPIATQIEPIGEFWLAAEEHQQYFEKKLKPNQN
>NZ_CP051167.1|WP_168570334.1|4388842_4390090_+|WD40-repeat-domain-containing-protein
MTDCPPQPKTYDLVLGGQNLPLSGAVLGGLDGVKQRLATAQVQQKINALHQALHYGQPGLELIVETLKDADPQIQKSAYLLLRERSEPEVKRALATVNPYEYLTRIDTLNGHKGLVLCVAFSPDGQTLATSGSGDKAIAMWDISSGKKLKTLQGHGDWVNAIAFNPQGPTCASCSSDGTIKIWDTSSGNPLGTLQGHTGAVYSLAYTPDGRTLVTGSADCTIDIWDLSQGRRSGSASLQRTLLGHQSRVEGVAVSPDGKIVASSSWDRTIQLWDLETGQSFQTLRAHQGLVVGVAFSPTGKHLVSYSTDTTIAVWKLFGRGLGTVATLQHTLCGHEERVNSVSIAPDGRTLIGGSRDGTISIWDLHRGELLGSVRSHSGWVNSVAYTVRTTYPQSRQKMLLASGGFGGAIELWTI
>NZ_CP051167.1|WP_168570335.1|4390471_4392781_-|response-regulator
MAKILVIDDDGATRLLLKRNLQLEGYQVFAAKDGREGLEQAREHRPDLIICDWVMPFYDGVEVCRQLKADPRLGNTFFILLTSSRGEINHRVEGLDAGADEFLSKPIDAEELSARVRAGLRLQQVTARLSEANRNLSALVRVQRRLLANESVCVPGRSLSGDGTQAEDRSRRSTGSVVADGFDLSRPQSHHLPRDANLLCPQDCHALDLLQPIGEAIGAERAFLWKFQPANGSFQISLGCCWLAGSPPCEESWERAAGFQFHEAWLERLRDGAIVAGYTADFPAEQRQNLQHAEVDSIAIVPLSIEGNCFGAIVFENCPETVAAYQSEGADGSSGDVCCPVTENSRFEPTSPIDMLRGAAAAIALHLDRSAALSALQASEARYRAIVEDQTELICRFDANGNLTFANEAYRRYFELDRCELNGGSHLPLSPDLERDLSESAAIERESSLVMSNGETRWQQWSERAIFDDRDRLLEFQAVGRDITERKRAEEETLKALGKEKELNELKTHFISMVSHEFKTPLTTIVSSADLLEFYLESVNHGTPEKLDNCLQRIQKAAIHMNELLEDVLTLARTESGRLECKPAPLNLNTFCQDLVEEFQGNHGDDLFLDFQCVGTLPEVCLDRKLLYHILSNLLSNAIKYSPENTAVEFRVFSEGDRAIFQVKDSGIGIPEEDLPYVFDAFQRCRNVGKIGGTGMGLAIVKRCVELHGGHVKVTSQLKGDRPSGGTTFTVAFPVDGNPRESLSLTSAAAIHREAPVGNSSGDRFHTHP
>NZ_CP051167.1|WP_168570336.1|4393057_4399591_-|PAS-domain-S-box-protein
MSDHSPVQILLVEDNNADAELLETWLLDVEKFRFNLTRASRLSEAIAHVENQSFDIILLDLSLPDSCGLETLHQLQQWNPTSWDGHSPRSSIALVPTIVLTGLDDEDVAIAAIHCEAQDYLVKGRFDGQLLVKSIRYAIERSSLSRQLKHLSEQLEHRVKERTAELEDAIASLEAEIRIRNQIEAALENSYNLLNGVVENSDDVIYVKNREGCYLLGNASLGKTLGCSIQDLFGKNDSELLPSDIAATLKEHDRQVVETGESRTFEEPIPVGGQWRIFSSNKSPYRNSKGEIVGSIGICRDMTDRVEMERQLKNFAEKQALLIEHTPLAAIEWNENLEIVAWNPSAERIFGYSREEAIGADRRLLFPDAEIETDEAIAILGSIGADGMGVVREHVTRDGRPVICEWYSTPIYQGGETIAGAISLILDISDRVRQEREIRDNEVEFRALFAAMNDIVIVLDDRGDCLKVAPTQEKLLYKPPEELVGKTLHEIFPIALADEFLNYIQTAIASQTPVKCEYWLPIGDRDICFDATISPMSAHTVIWVARDITDRQNAQQELRQYQNHLEELVRERTAELECANAELQAQIERRQQSETALRQSETRFRAIVEGTTVPLVITRNSDGTIFYTNQLFGELVGLSVSEAIGQSVRQFYADPDDRPRLLRQVERDGYVHSYELQFKPADGMLRWAMVSMQSIDFEGEDALLATFYDITQRKRIEEALAASERQYRYLVETSRDLIWSVDAQGCWTFLNPVARSIYGYDLEEMLGRPFSEFASPEQAQKDLEIFAGLLAGEHQSLVYETRHRRKDGRAVDLCYNVVVVRDRDGAIVGTTGTATDITERKRVEEALKFTQFSVDHAGDAICWATPEGRFLFVNESLCRYFGYTREELLNLSIADLDVKYGGDRWDEQWQNLKAAKTLTMETIGQTKAGTQRPFEVVANYLEYQGQEYLCAFLRDIGDRQEAERKLRDREQFLRSIWEGAGIPIFVLEVGEDGEFRYAGVNPIAAGYSPIPAAQLLGRTSREVLPPEIADPWNARYRECWQTGKPISFEEALVGGETCTWFLATLTPLRDGEGRIDRLICSAIDITDRRLADRALQESREQLDNILRSLDDIVWSTSADNSRIFYLNEAFERVYGRSLAEIHENPSIWFEAIAPEDREGLEPQGGKLWEKGSHDREYQIVRPDGERRWIRDRARVIRDEEGSAIRIDGIATDITERKTYEAALDRERRQLREIVTRAPVAMAMFDAPKEPLGERQWRYLAYSDRWVEEYDLGDESLVGRTLGETLPELARHWADPCDRAFNGEAISHPEDCLEIEDDRRIYLRWAIQPWYASAGEVGGIAIATHIIDELVEAREAALQTARLKAQFLANMSHEIRTPMNGVLGMTELLLHSSLTPQQRDIVETLRLSGQNLLALINDILDFSKLEVGEMRLEIHPFDLAEGLEELLNLFGPQAQAKGIGFAIVLDPQVERDRRGDLYHLKQILSNLLGNAVKFTQRGQILLRVRNAATPPGDERATVLRFEVDDTGIGIDRQDRDKLFTCFSQVDPSTTREYGGTGLGLAIAKQLVDLMGGEIGLESEPGRGSTFWFEVPLECNRDAEPNPEAGCLTGRRLLAVRERAADREAIAAWAAYWGVEVTEAADLRQALALVYTALTEERPFDFLAIDWAIVKSTPKLLERLLRGNAALAGTAAIAIGLFAEIEPLQALLNRGFAGYAIEPLVPSRLLQCLRGELVSPLPTPGQPRFSVGEATGTPLAPSSGLKVLLVEDTPINQKVVRGQLEVLGIAVEVACNGREALDRLARERYDLVLMDCQMPVLDGYDATRQLRAREGSATEHREGGEGRTTVVGLTAYAMKGDREKCLAAGMDDYLSKPVTVEDLEGILRRWTPWQPSHGVREPSPQENLAPVAVSPAAHAPNNGIPVDLAHLQKVSRGDRDFQRELVTVFLNDCNDYLAALKQGLTQGDAPQVARAAHQIKGASLSVGIRTIPDLVATLEEDARQGNITHTGAIATAIEAALERVRLWVAQFESISRDAEAIAVETPPVEPTPPQIASPPPSDPEECPVDRDRLHALSRGDRAFQIELLQAFVDDASGYLAKIDAALAASDAIALARHAHQLKGSSATVAIHSMPEIAHAIEQMAKQNQLDAVPDYMEELETIFERVRVFLRSLQTGKFDTNPE

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Crispr_ID: NZ_CP051167_23

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_23

4667793-4669506

Orphan

N:A

Consensus_repeat	Method
GTTTCAATCCCCTTACGGGGAGTTGGGCATAAGTGAC	PILER-CR
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CRISPRCasFinder
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CRT
GTTTCAATCCCCTTACGGGGAGTTGGGCATAAGTGAC	PILER-CR

21 spacers

The CRISPR arrays of NZ_CP051167_23

>merge|NZ_CP051167|23|4667793-4669506|PILER-CR,CRISPRCasFinder,CRT,PILER-CR
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACCATCAGCTGGTACTTGAATATCATGAGGTATACGATAGTCAGGAGTGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACGTCTGTGCCTGAAGAAGAAGCTCACGTTCCTTCAACAGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACTGAGGGAATACTTTCCGGCGACTAATAACCCCTTAGCGGCAGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACCTCCAGTTTTTCGAGCGAACCCTTTCACTGGTTTACCTCGAAGGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACACTTCCAGTGGGCTTTTCGCCCACTCAAGGACTTTTGCCGCTGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACTTCTGCTACAATGTGTGGAGATTTATTGAGGGAACATGGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACCATGGCCCACGTCAAGGCCATTTGCACTGATATATGCTGTATGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACGCCAGCTTCATCGAGCTTAACCCCTTCTTTCGTGTATCCTTCCGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACGAGTCTAGTGTTGCTCCAAGAGCTACGAGGTTATAAGCTTGAAGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACGGGGTGAATGTCAAGTACTCCCGCATCAAACAGGTCGAGCTTCCGTAACTCGACACCATATACGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACCCACTGGGGCGAAGGCGTCCGTATCACTCCACAATTGAGGGAGCGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACTCCTGCTCCCATGCGGTCTTAGGACCAACCGTTACAACCTCGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACTCGTACTCCTCTTGTAACTGCTCCAGGTATTCCACATACCTGAGAATGGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACACTTGTTCCATATAGCCACCTCAGCCTCATCAGCTTCCCAGGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACTCGTACTCCTCTTGTAACTGCTCCAGGTATTCCACATACCTGAGAATGGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACACTTGTTCCATATAGCCACCTCAGCCTCATCAGCTTCCCAGGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACCTATTTTCATATCATTCAATAATTAACAAGAACGCGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACCCTGGGATAATTCCCATTGCCATATCGAACAGCTTGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACAGTGCGAAGTCCTCATTCTCAAAGTTCATCGGCCCGTAATGCTGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACAGCGGTGCGACCTCCTCTGGGGGCAAGTTGTCGATACAAACCGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACCAGATTGCCTCAGCTTGCGGGGACATCGGATCAACTGGGAACAAGTCACTTATGCCCAACTCCCCGCAAGGGGATTGAAAC

>NZ_CP051167|23|19|4667793-4668457|PILER-CR
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CATCAGCTGGTACTTGAATATCATGAGGTATACGATAGTCAGGAGT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	GTCTGTGCCTGAAGAAGAAGCTCACGTTCCTTCAACA
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TGAGGGAATACTTTCCGGCGACTAATAACCCCTTAGCGGCA
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CTCCAGTTTTTCGAGCGAACCCTTTCACTGGTTTACCTCGAAG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	ACTTCCAGTGGGCTTTTCGCCCACTCAAGGACTTTTGCCGCT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TTCTGCTACAATGTGTGGAGATTTATTGAGGGAACATG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CATGGCCCACGTCAAGGCCATTTGCACTGATATATGCTGTAT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	GCCAGCTTCATCGAGCTTAACCCCTTCTTTCGTGTATCCTTCC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACGAGTCTAGTGTTGCTCCAAGAGCTACGAGGTTATAAGCTTGAAGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACGGGGTGAATGTCAAGTACTCCCGCATCAAACAGGTCGAGCTTCCGTAACTCGACACCATATACGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CCACTGGGGCGAAGGCGTCCGTATCACTCCACAATTGAGGGAGC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TCCTGCTCCCATGCGGTCTTAGGACCAACCGTTACAACCTC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TCGTACTCCTCTTGTAACTGCTCCAGGTATTCCACATACCTGAGAATG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	ACTTGTTCCATATAGCCACCTCAGCCTCATCAGCTTCCCAG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TCGTACTCCTCTTGTAACTGCTCCAGGTATTCCACATACCTGAGAATG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	ACTTGTTCCATATAGCCACCTCAGCCTCATCAGCTTCCCAG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CTATTTTCATATCATTCAATAATTAACAAGAACGC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CCTGGGATAATTCCCATTGCCATATCGAACAGCTT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	AGTGCGAAGTCCTCATTCTCAAAGTTCATCGGCCCGTAATGCT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	AGCGGTGCGACCTCCTCTGGGGGCAAGTTGTCGATACAAACC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CAGATTGCCTCAGCTTGCGGGGACATCGGATCAACTGGGAACAA


>NZ_CP051167|23|21|4667793-4669506|CRISPRCasFinder
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CATCAGCTGGTACTTGAATATCATGAGGTATACGATAGTCAGGAGT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	GTCTGTGCCTGAAGAAGAAGCTCACGTTCCTTCAACA
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TGAGGGAATACTTTCCGGCGACTAATAACCCCTTAGCGGCA
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CTCCAGTTTTTCGAGCGAACCCTTTCACTGGTTTACCTCGAAG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	ACTTCCAGTGGGCTTTTCGCCCACTCAAGGACTTTTGCCGCT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TTCTGCTACAATGTGTGGAGATTTATTGAGGGAACATG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CATGGCCCACGTCAAGGCCATTTGCACTGATATATGCTGTAT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	GCCAGCTTCATCGAGCTTAACCCCTTCTTTCGTGTATCCTTCC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	GAGTCTAGTGTTGCTCCAAGAGCTACGAGGTTATAAGCTTGAA
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	GGGGTGAATGTCAAGTACTCCCGCATCAAACAGGTCGAGCTTCCGTAACTCGACACCATATAC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CCACTGGGGCGAAGGCGTCCGTATCACTCCACAATTGAGGGAGC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TCCTGCTCCCATGCGGTCTTAGGACCAACCGTTACAACCTC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TCGTACTCCTCTTGTAACTGCTCCAGGTATTCCACATACCTGAGAATG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	ACTTGTTCCATATAGCCACCTCAGCCTCATCAGCTTCCCAG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TCGTACTCCTCTTGTAACTGCTCCAGGTATTCCACATACCTGAGAATG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	ACTTGTTCCATATAGCCACCTCAGCCTCATCAGCTTCCCAG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CTATTTTCATATCATTCAATAATTAACAAGAACGC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CCTGGGATAATTCCCATTGCCATATCGAACAGCTT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	AGTGCGAAGTCCTCATTCTCAAAGTTCATCGGCCCGTAATGCT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	AGCGGTGCGACCTCCTCTGGGGGCAAGTTGTCGATACAAACC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CAGATTGCCTCAGCTTGCGGGGACATCGGATCAACTGGGAACAA
GTCACTTATGCCCAACTCCCCGCAAGGGGATTGAAAC

>NZ_CP051167|23|12|4667793-4669506|CRT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CATCAGCTGGTACTTGAATATCATGAGGTATACGATAGTCAGGAGT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	GTCTGTGCCTGAAGAAGAAGCTCACGTTCCTTCAACA
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TGAGGGAATACTTTCCGGCGACTAATAACCCCTTAGCGGCA
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CTCCAGTTTTTCGAGCGAACCCTTTCACTGGTTTACCTCGAAG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	ACTTCCAGTGGGCTTTTCGCCCACTCAAGGACTTTTGCCGCT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TTCTGCTACAATGTGTGGAGATTTATTGAGGGAACATG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CATGGCCCACGTCAAGGCCATTTGCACTGATATATGCTGTAT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	GCCAGCTTCATCGAGCTTAACCCCTTCTTTCGTGTATCCTTCC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	GAGTCTAGTGTTGCTCCAAGAGCTACGAGGTTATAAGCTTGAA
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	GGGGTGAATGTCAAGTACTCCCGCATCAAACAGGTCGAGCTTCCGTAACTCGACACCATATAC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CCACTGGGGCGAAGGCGTCCGTATCACTCCACAATTGAGGGAGC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TCCTGCTCCCATGCGGTCTTAGGACCAACCGTTACAACCTC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TCGTACTCCTCTTGTAACTGCTCCAGGTATTCCACATACCTGAGAATG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	ACTTGTTCCATATAGCCACCTCAGCCTCATCAGCTTCCCAG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TCGTACTCCTCTTGTAACTGCTCCAGGTATTCCACATACCTGAGAATG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	ACTTGTTCCATATAGCCACCTCAGCCTCATCAGCTTCCCAG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CTATTTTCATATCATTCAATAATTAACAAGAACGC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CCTGGGATAATTCCCATTGCCATATCGAACAGCTT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	AGTGCGAAGTCCTCATTCTCAAAGTTCATCGGCCCGTAATGCT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	AGCGGTGCGACCTCCTCTGGGGGCAAGTTGTCGATACAAACC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CAGATTGCCTCAGCTTGCGGGGACATCGGATCAACTGGGAACAA
GTCACTTATGCCCAACTCCCCGCAAGGGGATTGAAAC

>NZ_CP051167|23|20|4668601-4669506|PILER-CR
	CATCAGCTGGTACTTGAATATCATGAGGTATACGATAGTCAGGAGT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	GTCTGTGCCTGAAGAAGAAGCTCACGTTCCTTCAACA
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TGAGGGAATACTTTCCGGCGACTAATAACCCCTTAGCGGCA
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CTCCAGTTTTTCGAGCGAACCCTTTCACTGGTTTACCTCGAAG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	ACTTCCAGTGGGCTTTTCGCCCACTCAAGGACTTTTGCCGCT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TTCTGCTACAATGTGTGGAGATTTATTGAGGGAACATG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CATGGCCCACGTCAAGGCCATTTGCACTGATATATGCTGTAT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	GCCAGCTTCATCGAGCTTAACCCCTTCTTTCGTGTATCCTTCC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACGAGTCTAGTGTTGCTCCAAGAGCTACGAGGTTATAAGCTTGAAGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAACGGGGTGAATGTCAAGTACTCCCGCATCAAACAGGTCGAGCTTCCGTAACTCGACACCATATACGTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CCACTGGGGCGAAGGCGTCCGTATCACTCCACAATTGAGGGAGC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TCCTGCTCCCATGCGGTCTTAGGACCAACCGTTACAACCTC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TCGTACTCCTCTTGTAACTGCTCCAGGTATTCCACATACCTGAGAATG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	ACTTGTTCCATATAGCCACCTCAGCCTCATCAGCTTCCCAG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	TCGTACTCCTCTTGTAACTGCTCCAGGTATTCCACATACCTGAGAATG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	ACTTGTTCCATATAGCCACCTCAGCCTCATCAGCTTCCCAG
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CTATTTTCATATCATTCAATAATTAACAAGAACGC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CCTGGGATAATTCCCATTGCCATATCGAACAGCTT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	AGTGCGAAGTCCTCATTCTCAAAGTTCATCGGCCCGTAATGCT
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	AGCGGTGCGACCTCCTCTGGGGGCAAGTTGTCGATACAAACC
GTCACTTATGCCCAACTCCCCGTAAGGGGATTGAAAC	CAGATTGCCTCAGCTTGCGGGGACATCGGATCAACTGGGAACAA
GTCACTTATGCCCAACTCCCCGCAAGGGGATTGAAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168570522.1\|4662786_4663827_-\|sulfate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270226
NZ_CP051167.1\|WP_168570523.1\|4663873_4664899_-\|sulfate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270226
NZ_CP051167.1\|WP_168570533.1\|4686223_4686601_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570531.1\|4680480_4683990_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238121
NZ_CP051167.1\|WP_168570520.1\|4661073_4661937_-\|sulfate-ABC-transporter-permease-subunit-CysW	unknown	unknown	gnl\|CDD\|226665
NZ_CP051167.1\|WP_168570535.1\|4687103_4687727_-\|J-domain-containing-protein	unknown	unknown	gnl\|CDD\|223560
NZ_CP051167.1\|WP_168570519.1\|4657289_4660991_-\|helicase	unknown	unknown	gnl\|CDD\|365992
NZ_CP051167.1\|WP_168570526.1\|4666457_4667480_+\|tRNA-dihydrouridine(20/20a)-synthase-DusA	unknown	unknown	gnl\|CDD\|236991
NZ_CP051167.1\|WP_168570524.1\|4665144_4666161_-\|sulfate-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|213263
NZ_CP051167.1\|WP_168570536.1\|4688017_4688614_-\|ATP-dependent-Clp-protease-proteolytic-subunit	unknown	unknown	gnl\|CDD\|178955
NZ_CP051167.1\|WP_168570521.1\|4661929_4662727_-\|sulfate-ABC-transporter-permease-subunit-CysT	unknown	unknown	gnl\|CDD\|131194
NZ_CP051167.1\|WP_168570534.1\|4686621_4686960_-\|antibiotic-biosynthesis-monooxygenase	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570530.1\|4679023_4680052_+\|dihydroorotase	unknown	unknown	gnl\|CDD\|235474
NZ_CP051167.1\|WP_168570532.1\|4684525_4685836_-\|serine/threonine-protein-kinase	unknown	unknown	gnl\|CDD\|373105
NZ_CP051167.1\|WP_168570518.1\|4654179_4655316_+\|succinylglutamate-desuccinylase/aspartoacylase-family-protein	unknown	unknown	gnl\|CDD\|349468
NZ_CP051167.1\|WP_168570528.1\|4671104_4678025_+\|DUF4347-domain-containing-protein	unknown	unknown	gnl\|CDD\|372982
NZ_CP051167.1\|WP_168570527.1\|4670197_4670377_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224854
NZ_CP051167.1\|WP_168570525.1\|4666213_4666360_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570529.1\|4678485_4678677_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571960.1\|4655377_4657252_+\|excinuclease-ABC-subunit-UvrC	unknown	unknown	gnl\|CDD\|234792

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168570522.1\|4662786_4663827_-\|sulfate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270226	cd01005, PBP2_CysP, Substrate binding domain of an active sulfate transporter, a member of the type 2 periplasmic binding fold superfamily. This family contains sulfate binding domain of CysP proteins that serve as initial receptors in the ABC transport of sulfate and thiosulfate in eubacteria. After binding the ligand, CysP interacts with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The CysP proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	3.26805e-143
NZ_CP051167.1\|WP_168570528.1\|4671104_4678025_+\|DUF4347-domain-containing-protein	gnl\|CDD\|372982	pfam14252, DUF4347, Domain of unknown function (DUF4347). This domain family is found in bacteria and eukaryotes, and is approximately 160 amino acids in length. There are two completely conserved residues (C and G) that may be functionally important.	1.10382e-56
NZ_CP051167.1\|WP_168570536.1\|4688017_4688614_-\|ATP-dependent-Clp-protease-proteolytic-subunit	gnl\|CDD\|178955	PRK00277, clpP, ATP-dependent Clp protease proteolytic subunit; Reviewed.	2.44127e-128
NZ_CP051167.1\|WP_168570531.1\|4680480_4683990_-\|hypothetical-protein	gnl\|CDD\|238121	cd00200, WD40, WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from its N-terminus and the WD dipeptide at its C-terminus and is 40 residues long, hence the name WD40; between GH and WD lies a conserved core; serves as a stable propeller-like platform to which proteins can bind either stably or reversibly; forms a propeller-like structure with several blades where each blade is composed of a four-stranded anti-parallel b-sheet; instances with few detectable copies are hypothesized to form larger structures by dimerization; each WD40 sequence repeat forms the first three strands of one blade and the last strand in the next blade; the last C-terminal WD40 repeat completes the blade structure of the first WD40 repeat to create the closed ring propeller-structure; residues on the top and bottom surface of the propeller are proposed to coordinate interactions with other proteins and/or small ligands; 7 copies of the repeat are present in this alignment.	1.39264e-101
NZ_CP051167.1\|WP_168570520.1\|4661073_4661937_-\|sulfate-ABC-transporter-permease-subunit-CysW	gnl\|CDD\|226665	COG4208, CysW, ABC-type sulfate transport system, permease component [Inorganic ion transport and metabolism].	2.55387e-132
NZ_CP051167.1\|WP_168570535.1\|4687103_4687727_-\|J-domain-containing-protein	gnl\|CDD\|223560	COG0484, DnaJ, DnaJ-class molecular chaperone with C-terminal Zn finger domain [Posttranslational modification, protein turnover, chaperones].	1.91702e-21
NZ_CP051167.1\|WP_168570519.1\|4657289_4660991_-\|helicase	gnl\|CDD\|365992	pfam00271, Helicase_C, Helicase conserved C-terminal domain. The Prosite family is restricted to DEAD/H helicases, whereas this domain family is found in a wide variety of helicases and helicase related proteins. It may be that this is not an autonomously folding unit, but an integral part of the helicase.	0.000105383
NZ_CP051167.1\|WP_168570526.1\|4666457_4667480_+\|tRNA-dihydrouridine(20/20a)-synthase-DusA	gnl\|CDD\|236991	PRK11815, PRK11815, tRNA dihydrouridine(20/20a) synthase DusA.	0
NZ_CP051167.1\|WP_168570532.1\|4684525_4685836_-\|serine/threonine-protein-kinase	gnl\|CDD\|373105	pfam14516, AAA_35, AAA-like domain. This family of proteins are part of the AAA superfamily.	9.68403e-172
NZ_CP051167.1\|WP_168570521.1\|4661929_4662727_-\|sulfate-ABC-transporter-permease-subunit-CysT	gnl\|CDD\|131194	TIGR02139, permease_CysT, sulfate ABC transporter, permease protein CysT. This model represents CysT, one of two homologous, tandem permeases in the sulfate ABC transporter system; the other is CysW (TIGR02140). The sulfate transporter has been described in E. coli as transporting sulfate, thiosulfate, selenate, and selenite. Sulfate transporters may also transport molybdate ion if a specific molybdate transporter is not present. [Transport and binding proteins, Anions].	5.99411e-131
NZ_CP051167.1\|WP_168570518.1\|4654179_4655316_+\|succinylglutamate-desuccinylase/aspartoacylase-family-protein	gnl\|CDD\|349468	cd06250, M14_PaAOTO_like, Peptidase M14 Succinylglutamate desuccinylase (ASTE)/aspartoacylase (ASPA)-like subfamily; subgroup includes Pseudomonas aeruginosa AotO. An uncharacterized subgroup of the Succinylglutamate desuccinylase (ASTE)/aspartoacylase (ASPA) subfamily which is part of the the M14 family of metallocarboxypeptidases. This subgroup includes Pseudomonas aeruginosa AotO and related proteins. ASTE catalyzes the fifth and last step in arginine catabolism by the arginine succinyltransferase pathway, and aspartoacylase (ASPA, also known as aminoacylase 2, and ACY-2; EC:3.5.1.15) cleaves N-acetyl L-aspartic acid (NAA) into aspartate and acetate. NAA is abundant in the brain, and hydrolysis of NAA by ASPA may help maintain white matter. ASPA is an NAA scavenger in other tissues. Mutations in the gene encoding ASPA cause Canavan disease (CD), a fatal progressive neurodegenerative disorder involving dysmyelination and spongiform degeneration of white matter in children. This enzyme binds zinc which is necessary for activity. Measurement of elevated NAA levels in urine is used in the diagnosis of CD. The gene encoding P. aeruginosa AotO was characterized as part of an operon encoding an arginine and ornithine transport system, however it is not essential for arginine and ornithine uptake.	2.20257e-63
NZ_CP051167.1\|WP_168571960.1\|4655377_4657252_+\|excinuclease-ABC-subunit-UvrC	gnl\|CDD\|234792	PRK00558, uvrC, excinuclease ABC subunit UvrC.	0
NZ_CP051167.1\|WP_168570527.1\|4670197_4670377_-\|hypothetical-protein	gnl\|CDD\|224854	COG1943, COG1943, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	9.52372e-07
NZ_CP051167.1\|WP_168570524.1\|4665144_4666161_-\|sulfate-ABC-transporter-ATP-binding-protein	gnl\|CDD\|213263	cd03296, ABC_CysA_sulfate_importer, ATP-binding cassette domain of the sulfate transporter. Part of the ABC transporter complex cysAWTP involved in sulfate import. Responsible for energy coupling to the transport system. The complex is composed of two ATP-binding proteins (cysA), two transmembrane proteins (cysT and cysW), and a solute-binding protein (cysP). ABC transporters are a large family of proteins involved in the transport of a wide variety of different compounds, like sugars, ions, peptides, and more complex organic molecules. The nucleotide binding domain shows the highest similarity between all members of the family. ABC transporters are a subset of nucleotide hydrolases that contain a signature motif, Q-loop, and H-loop/switch region, in addition to, the Walker A motif/P-loop and Walker B motif commonly found in a number of ATP- and GTP-binding and hydrolyzing proteins.	1.47145e-152
NZ_CP051167.1\|WP_168570530.1\|4679023_4680052_+\|dihydroorotase	gnl\|CDD\|235474	PRK05451, PRK05451, dihydroorotase; Provisional.	0
NZ_CP051167.1\|WP_168570523.1\|4663873_4664899_-\|sulfate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270226	cd01005, PBP2_CysP, Substrate binding domain of an active sulfate transporter, a member of the type 2 periplasmic binding fold superfamily. This family contains sulfate binding domain of CysP proteins that serve as initial receptors in the ABC transport of sulfate and thiosulfate in eubacteria. After binding the ligand, CysP interacts with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The CysP proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.14689e-154

>NZ_CP051167.1|WP_168570526.1|4666457_4667480_+|tRNA-dihydrouridine(20/20a)-synthase-DusA
MTSTLPRSAPVLDSPDDRPAGRPLSVAPMMDRTDRHFRYFMRQITRETLLYTEMVVSAAIIHGDRDRLLGFSPEEKPLALQIGGDDPRELAECARIAEDFGYDELNLNVGCPSSRVQNGNFGACLMARPERVAEAVAAMQAATRLPVTVKHRIGIDDRDRYEDMAHFVSVVAEAGCRRFTVHARKAWLSGLNPKENRNVPPLRYADVYRLKREFPHLWIEINGGIKTVAQIEQQLQQVDAVMVGRAAYDDPYLFAPCDRAIFGVASAPPTRHEVVERMLPYIDRCVGAGVRLHKISRHLLQLFAGQPGSRAWKRHISEHACRPGAGSTVICEALARVPRG
>NZ_CP051167.1|WP_168570525.1|4666213_4666360_+|hypothetical-protein
MTRDPQVGRDGTIASAKIYGKLVGILYFYSIPRRSPDRPSPLFLQKLS
>NZ_CP051167.1|WP_168570524.1|4665144_4666161_-|sulfate-ABC-transporter-ATP-binding-protein
MGIVVENVSKRFGNFAAVDSVSLTVKTGCLMALLGPSGSGKSTLLRLISGLETPDSGKIWLIGQDATYQSVQERNIGFVFQHYALFKHLTVRQNIAFGLEIRKLPKAKVKRRVEQLLNLIQLEGLGDRYPNQLSGGQRQRVALARALAVEPQVLLLDEPFGALDAKVRKDLRAWLRRLHDEVHVTTVFVTHDQEEAMEVADEIAIFNQGHIEQVGSPSEIYDRPATPFVMSFIGPVNVLPSHSRIFQDRPVDGAGKQVFVRSHDVAVAPVASDNSAPARVVRIVNLGWEIQAELQLDDGQMVVAHLSRERFDELNLEPQQRVFVSPREAKSFPLDYSI
>NZ_CP051167.1|WP_168570523.1|4663873_4664899_-|sulfate-ABC-transporter-substrate-binding-protein
MNWHRSIALLLVGTFSGVAIAACTGGERSSENSLELTLVSYAVTRAAYENIIPKFTAEWKEKHGQDITFTQSYGGSGSQTRAVVDGLEADIVALALALDTQKIEEAGLIDPGWENEAPNGAIVHKSVAALVTREGNPKQIETWQDLAKPDVATITANPKTSGGARWNFLALWGAATRTRGDETAAENFVTQVFKNVPILPRDARESSDVFFKQGQGDVLINYENEVILAAINGQKLPYVVPDVNISIDNPIAVVDANVDRHGTREVAEAFVEYLFTPAAQREFAKVGFRPVDASVAEEFKEQYPEVKTLFTVEDLGGWDQVQTQFFDEGALFDKMLAEINR
>NZ_CP051167.1|WP_168570522.1|4662786_4663827_-|sulfate-ABC-transporter-substrate-binding-protein
MNKNRSCWRIFPALTLGIGTVLIGAIAGCSPSEKSENTVELTLVSYMVTHAAYQHIIPQFAEQWQRDRGQTVVVRESYGASGNQTRTVLHGLEADVVALALTLDIRQIEKAGLIDPGWEQEAPNGAIVTRSVPALAVREGNPQQIKTWADLAKTGVTVLTPNPKTSGVARWNFLALWGSVTETGGSPEEALQFTRNVFANAPALPKDAREATDIFFRDHRADVLINYENELILAQLNDRPIAYFVPEVNLAIEHAVAVVDRNVEAHGNREVAEAFVRYLFTPEAQREFAKVGFRPVDPTVAAEFADRYPPVKNLYTIEDLGGWDALQAQFFDEGGIFDRIEAAIGP
>NZ_CP051167.1|WP_168570521.1|4661929_4662727_-|sulfate-ABC-transporter-permease-subunit-CysT
MKHISWPWRITFGYMTIMLLLPIAALLLSASTKGFAEFWRIATSPIAIAAYDVTFITALLAAGLNGIFGTLIAWVLVRYEFPFKRIVDATIDLPFALPTAVAGLSLATVYSENGWIGSLLAPLGIKIAFTRLGVWVAMLFISLPFVVRTLQPVLREIEPEIEECAWCLGASKSQTFWRVLLPQMISPILIGVALGFSRAVGEYGSIVIVASNIPFKDLIAPVLVFQRLEQYDYYGATVIGTVLLVVSLLILLAINLLQTWGRRYA
>NZ_CP051167.1|WP_168570520.1|4661073_4661937_-|sulfate-ABC-transporter-permease-subunit-CysW
MHEVNQDRSNLAIYHHQKQIDWGKIIAIAVAIVYLGLVLLIPAINVFFQAFRKGIAPFLHNLAEPAFLHAVTLTVIVAAIVIPINTVFGLCAAWAIARDKIPGRTLITSVIDLPFSVSPVVAGLAIVLLYGRNGWFASILDFANIKVIFALPGIVIATLFITLPFVARSVIPVLEETGADQEEAAKTLGATDWQIFWRVTLPNIRWGLLYGLILTNARAMGEFGAVAVVSGNIIRKTQTLPLFVEEAYKQYQTQAAFSAAVLLSCLGVVTLVLKEILERKTKIEDLR
>NZ_CP051167.1|WP_168570519.1|4657289_4660991_-|helicase
MEELGRFFEVGFNIGILAEIERRNLRHPFGSCYRQELASLRLSKIVRRIVKKYEAIAPQNVAIVTQWTQFFLLKGFVSGLNFLREYLKATNWKKRQLEQVEILYYQCNFGNDNTVGTSQKSERDRIRDYFAQLGMGEESDRLTLQYKGKGQFLQADTLLWLRHRQKHRIVCVDLSVFSVKSAADLVPLDEIEMLRQLLATEIKYLRSKSVFSKLRIDTGQQEDFDLHFSQDLMRYFTAFKRKDKESAKLIQAGSYAYSFYQFLQQFGRLKDAKSLILNVVGYSDRQISNLSISLDNIDLLKTCAYIYKNEPSNAQIQETRHQVLEIVRRNAAKSFENGTHLVNQLLDILSNHSANGISQVVHQEHLDNFVNSIGIVDDDLADRLQVERGSQLRSAHAQLIEKALNSDDIYLFLTGNPGIGKTTAIANFLKQHFDEGFLFLYISPRKQVNLDILEKFKDKTGNLCDDRLFCITSNSVIIKENNGLKTVLYHANKSQNHFTLNTVNFIPINDRNTNSKKSERPTSLEQTRQDTIRSLKNRSSGVLQSLCEALNGIVTQEISNHTIATVAIQSLRMTGEESSTLTHLDRIFASAYNSREERVIPEKMAAISRRIKHLFIAIDEITGDDSGVSFFKGIREFINKFNLAEYGFNLKIIVADASIVDSQVIEQHLSDSSPELDKIYVRRTKSDIEPLSVKEFNFHRNKARSINTNSYPASSLDFTYKVFLETIEFSQNPFKYDANNALVSSIQERIFKDICNLLDREGSAQILVYIQDKRRLQELIEQLKNQRKQFQYCSDYLEIHANLSDPEKSLIQQYKQDAKVIFMTSSASRGLSFPKARHILVDIPQFQIERNLMEVIQVIYRARGNYWENEELKTLDNLSKEIIFYLGDRAIYYPGTSESYSEEEMKLSKAFSRQESLLNVLNILLVLKVSILTRIVGAGRLGRKKDYSIIPIGGKSVSASGMTFTDRMANLIRQLKNEHRRLPSHQQLKRVYTSLEKLLDRAEFVLDKRSQQDFQETYLSLKNSFFSKFVEACHRFDRLLDLKDIETGYLNGNLLVVPISNRRLEESYTIALETQIKQYATPDLIEDMRAIGRNQQYPENLQAAIEDGALELIELLEGERSQSQYLELNSAESDRYYAIPLFAFVSSETLRDYFKNYPRDLEDHRRFRSLLSSYVRCLYPVYNTLPIGYKYEEFPFLIFRSYSLEQIRYKMFADRYLLRSHELNVLNLILAKE
>NZ_CP051167.1|WP_168571960.1|4655377_4657252_+|excinuclease-ABC-subunit-UvrC
MTSSLSTVPLIKDPDRLESRLKEIPPVPGVYFMRDNNDRILYIGKSKKLRSRVRSYFRDSQQLSPRIALMVQQVCEIEFIVTDTEAESLALEANLIKQHQPNFNVLLKDDKKYPYLCITWSEDYPRIFITRKRKLGNRKDRYYGPYVDSTALRNTLHLVKQIFPLRQRPQPLFKNRPCLNYDIGRCPGVCQQLISPEDYRQIVQKVAMVFQGRTEELVGILSEQMQQAAEALNFEQAAKLRDRIAGLNSLNSDQKVALPDDRISRDAIALAKNRHHACIQLFQIRAGQLVGRLGFVTSAENAESGEILQRVLEEHYQHVESVEIPTEILVQSDLTDGPMLAEWLSDRKGRKVAIVTPQRQTKADLLEMVERNAEYELQRLQRQSDRNAEALQDLAELLDLPDWPRRIECYDISHIQGSDAVASRVVFVDGMPAKQHYRRYKIRNPEVRSGHSDDFASLAEVLGRRFRHSRGDLDLCINAPDWPDLVAIDGGKGQLSTVVEVLEQLEIADVLTVVSLAKQREEIFRPGESAPVPSDPEQPGVQLLRRVRDEAHRFAVTFHRQQRGDRMRRSRLDEIPGLGFQRQKQLLAHFHSIDYLRVATPEQIAEVPGIGPRLARQIYEYFHP
>NZ_CP051167.1|WP_168570518.1|4654179_4655316_+|succinylglutamate-desuccinylase/aspartoacylase-family-protein
MLPEISTLPILQLASGDYLSLQVYHFRGDRPGKKAYLQSNLHGCEISGNAVLHELINFLQSLDRTQLEGEVVIVPACNPMAMNARSHHFSSGRYNPYDGRDWNRIFWDYHKVSHDLDEIARDFCELEVETIRKEYLKLIQTTFNRHHDNLDSASGVPLHKRYRYLLQSLCLDANYVIDCHSSSNRTIDYFYCFHDREESAKYFLIDLGIFLESYDGYTFDEAFLKPWLALEKALAKQGRKIIFDLESWTLELGGGMEVNSQSVAKGVRGIKNYLAGKKMLTISGFPLAETHQHQVQFFHKHQLRRYHAVAGGILRDRLPLGTVVKAGDRLYTLLSFNKNGECPTQVAIEAERDGIIYDLSLNESVNQSDYVLSIFEDH
>NZ_CP051167.1|WP_168570527.1|4670197_4670377_-|hypothetical-protein
MNLETTISASRKARRERNLWQRRFWEHRVRDEQEFAAYCDYIHINPVKHGLCKSPTDWP
>NZ_CP051167.1|WP_168570528.1|4671104_4678025_+|DUF4347-domain-containing-protein
MLKMSGPTDKRSHGICDRSSKTVKELVIVDAQVEQWEILASGVRPECEVVVLHPHEDGIQQIAALLTADRPDGIQSGSLSTIHIISHGSADTLYLGNSILNRETLETLYSQAIQQWRQVLSDNAHILIYGCNVAAIDADASSQTSLLSLLRELTGANIAASSTAIGNAAQGGNWNLDYSTDPKQPALAFLPEVMANYPAVLGKGPGGVGTTDGTSTLELWLKGDAGVTQTANAVSAWGDQSGNGVSLDQPTAASQPTYNATGLNNQPTLTFDGTDDYLETAFNANLNSPQFDLFVVTKATGGAGTFRSVITSREVTPEARGYSLYAADVNTWQHWTGDGAAAWVKGGSSPVTADSWEVIAGNYDGTTQRTFTNGAEVDSIATTYPPNTSNPTRIGAGFRAGDPSLDFYLPGEIAEVLIYSNALNTAERTIVDNYLSSKYALTTATDKYVGDNAANGDYDLNVAGIGQEANGNNTTATSADLTIANNTYLQDNGDYLLFGHNQATNSLVTTDIPTGTTNRWNRVWYLDKTDTNTNNGTVDLTFDFSELGSTPTGTYTLLFRNGTTGAFSAVAGVTAGTISGNQVVFSGVDLSALADGYYTLGSDSSAPTLSSVSIASNNANDTSLAKVGDTVTVTFTASDPLSGTPTVTIGGQTATVTNTTGNTYEATYTLTDSDTEGAQAINIQFSDAGGNTGTATATTDSSSVSLDKTAPSLSAVSIASNNANDTSTATVGDTVTVTFTASETLSGTPTVTIGGQTATVTNTTGNSYEATYTLADGDSTGALGFNINFTDVVGNTGTSAATTDSSSVTFNATPDSIGLAFDNSEVITNPLNLGFTKLQESLTDSLGKLPIVGESVQTAVPNFFNNIKNQLSTGLSVSQVWDAAKFKQAIQDALSQDFANVTVSESVGANGELQAIVNLSQQYNPTVGLNGDLGLPGLKLNAQGDANTKFNYDFSLGLGLNEQGLFFDTNNTTLSLNTEASLADNFQGTSDVSLLPINLANNTNNPTQLTGDFQLSLQDLTADLGGVNDGKLTFSELDQGTYDLSYLIDTTLNTKGTLGFKARTNLGESAAIPSYSFDLNANFPELNYANGQWSGPQIPKLAFNNIQLDLGTFVADFAEPVMSTIDDIISPIKPLLTVFNGNIEPLSHFGIVREFFDINEDGKVTLIEVGAKITGNDIDTSFLDSLEYVIQANSLLVDLANSGGNITIDLGDYELDFDPTNPNAELKNAPKTQVKTTASSLEQAKSNSTTQELFNLFGKMDGLSFPILTPDNSVDLLLGKEDVTLFAYKLPDLDFEFNLGEEFPIFSIPVVNVGVNGTFGIDLAATSNLGFGFDTYGLAEWKKSGGTDYSKIFDGFYVSDRQNADGTGDDVHELKLTGGINLGGGVNVALAKAYLTGGLEANIKFDLLDVGEGEFSSSQFDGLREEVRAVLNEYSHLGVDPNLADDLNMNAENLYEEGKAKIREPAGSSVSAENVDTVRNEMWWKVHDVLGKVYNSSVEKALGTGDGKIRASEITSRISRPLSLFAINGDLKAVLDFVAEYYVPLSWYTAYEKRLAEVTLAEFRLGDYTSNKSRAIDPYISGGFVFFDANFNEVFDEDTEPFALTNPDGSFELDIQLDSFDLNGNGTIDPTEGQIILNEGVDASTYLPLVTPLTSIPGSEVVTPLTTMIAWLVEDGLDPASAENQVKTALGLPAEVNLSTYDPLFAIANGDPNGVAVFAAMIQVQNTIVQTAKLIEGGSDIAVVQLGHAAISGIAKFLKSNSSVDLTQLETIEAIVQDAISFSPSFGSEGNTVNAEQISSVASAAAEVMALGNQIVQELSTSGLPLTDIATEITKMQAVAVGQIAVGLPELAAGTLPVEEFLANNTKEAIEQKMAEVRVADPTVRPTFPSFNIEVDPAGPQLEDPSELSPWLPQQLLTNNDGEQLSDDKQIETAQPRKLSILLFDPAYYLAENVDVADAVANGTVRSAAEHFSLFGLAEGRSPSEVFTNLYLANNPDVADAVTNGSFRSAFQHFIKFGFAEGRFPSDLFKDFEMFYVSQNADAAEAIANGTYSNGLEHLVSVGFAEGRNPFVQFEMLTQTFDAKYYLSQNADVADAVENGIFRNAMEHFIYFGLSEGRNPSLAFSNPIYLANNPDVESAINEGSFASGYAHYLMHGFAEGRIGGAIAVNARTNFNLGDRALLTEQETDLLTGMDENTINSDLGDVDQLIGQPGAETFILGDANQAYYLNSADAVSGKEYAIVTNFDTSEDIIQLQGVSADYELAASPAGIPSGTAIYRNEGDSKDLIAVVQDVSELSLQSDYFSFV
>NZ_CP051167.1|WP_168570529.1|4678485_4678677_+|hypothetical-protein
MSKIGSIPIDGNGIKSFGAFQLHLLQLLPPQAKSIEKTIAAIDPLTTHQPHRKPHRLFADTCP
>NZ_CP051167.1|WP_168570530.1|4679023_4680052_+|dihydroorotase
MQQLTLTRPDDWHLHLRDGAALKVVLPHTVRQFARAIIMPNLKPPVRSLADAAAYRDRILAAIPAGKQFEPLMTLYLTDNTSPEETIAAKASGFVKAVKYYPSGATTNSEFGVTDIRKCDRVFEAMQQVDLPLLLHGEVTDKDVDIFDREKVFIQRYLIPLKQRFPKLRVVLEHITTADAVEYVLNANNIGATITPQHLLFNRNRIFKGGINPHFYCLPILKRETHRQALVKAATSGNPKFFLGTDSAPHTRTSKESACGCAGCFSALHAIELYAEAFESVNALDKLEAFASFYGPDFYQLPRNTEQITLNKSTWKIPDEVPFTESGLVPLNAGQEMTWQMV
>NZ_CP051167.1|WP_168570531.1|4680480_4683990_-|hypothetical-protein
MPDSDYQVGGSLPSDAPTYVVRQADERLYRALKNGEFCYVLNCRQMGKSSLKVRTMQRLQAEGFSCGAIDITLLGTQEVTIQQWYGSAIVTLSQNFDRLRSFNPLKWLGDRAQLSPVQWFSEFIDRVILDAIDGNIVIFIDEIDSLISLNFKDDFLAFIRACYNQRSHDSRYNRLSFCLLGVATPSDLIRDKSKTPFNIGHPIELTGIQFEEAEPLLIPGLRDRFDHPETVLREILNWTGGQPFLTQKLCRLSIEDLDRNDPDLDCLVYNKILDNWEAQDQPEHLKTIRDRLFYDDRQTGRLLGLYQKVLLSGDRPFPAEGSREENLLRLSGLIVKGDRGLRVANRIYREVFNRDWIERSLAHLRPYSEALNAWLTSDRKDSSRLLRGRALQEALTWANDKSLSDLDYQFLAASQEQEKQEVQKELEVQRRASEILATANKTLKDAQIKAKRTIQTGALILVGILLGSTLIVWGAASQAKKAEIDELKALNSASKFNRESNQQLKALVNAVRAARKLQALRVDAEIREQTIANLEQLLSEIDEYNRLDEQEGWVWNVAFSPDGDRLATAAEAKVRIWSDNGELEGVLDHDDRVYGLAFSPDGQTLATASKDGTVRLWSDDGELLHRLDAHQESVFAVAFSPDGRYVASASEDKTIAIWGVDGSLKGRLSGHTQSIYSLSFSPDGKLLASASEDNTVRVWPFPIPEEQEKITPIDILTEHKFDVTGVSFAPNGDRLASADSNGTIHLWQFDPKTQKFLLKERFKDHENVIWMLAWSPDSRTLGSASADKTVKFWSLDGTLLKTLEGHDDAVLALSFSPKDGLVATGSSDRTVKLWKPQIRLVEVFDNGETMVNGIDFAPDGGAIASASRDNQVRLWNLDGTVRQTFSGHTNWVYDVSFSPDGQFLASASKDKTVKLWNLQGKAIRTLEGHGDEVNAVAISPDSQQIASASFDRTIKLWNRDGEAIGDLTGHQNWVYDVTFSPDGQMLASASKDKTVKLWSRDGTLLETLEGHANEVNAVAFSPDGEFLASASDDNTVKIWQLDGTLVRTLRGHTNKILDVTFSPDGELIASGSDDNTIKIWTRKGDLLATLSEHTNRVWSVRFSPNGYSLASGSWDRTVKLWALGDVRLQLEEAMDRNQSDLDRLLGNACDRLQDYLEFHLESRVCDRVL
>NZ_CP051167.1|WP_168570532.1|4684525_4685836_-|serine/threonine-protein-kinase
MQEQAIDLEQALQVADEAVFTKTDKHLTDVEIAIFRGAWQNQTYQEMAENTDYSANYLHRVVGQKLWDRLSDALEEKVSKKNFRAALERRWRSQHSPNSHAGFAADRPFSIDLPDIEKRCYHAIAQPGALLRIKAPKRTGKTLLSAKILDFAARQGYRTAYLNLNLASQSDFTNLDRFFQWFCVSVAQMLQLPARLNDYWNSQILTSKMNCTQYFENYLLAGDAPPLVLCLDEVDLLFPHTLVAQEFLGLLRGWHEQAKVRNIWQKLHLIFVYSTEVYISLKIEDSPFNVGVPIELPEFNREQVLRLARAYGLQWSESDVSALMAMVGGHPFLVQQAISNLKNQPGMTLAEILATAPTEAGIYNHHLRRLWLHLQAHPNLLDAFKKAIASDNPVNLERTEGYQLHGVGLLQLRGNNYIPRCDLYLQYFRDRFESSG
>NZ_CP051167.1|WP_168570533.1|4686223_4686601_+|hypothetical-protein
MYFLILNDLDPELQDLFPEGVPTFSATPDEFVEIYDESGLELVDIQPAFRVNLGGLSADRELKLLAAYTSEMNDPHFIRGCFKLLDKGWVTIPEDRVASVVWRYGDYVFSAVRDGSSAIADPVEC
>NZ_CP051167.1|WP_168570534.1|4686621_4686960_-|antibiotic-biosynthesis-monooxygenase
MSEFLDFLQHKCAYVAIGEFKPGKFAEARHLYEKAVSTYRDGFQGAYLLQEPGTDKGIAVVFWDNIADMEANRNQVHDAILQEMSDLFLYPPTTNFYEVCSEIDSPAKSVGV
>NZ_CP051167.1|WP_168570535.1|4687103_4687727_-|J-domain-containing-protein
MNIRECYQLLGLSAGATLADLKSSYRKLARRYHPDVNRGDRGCHEKFIEINQAYQILLQALESTPVSANPAGSPTASATPRRSSPPPPPPPPRVVRKEPSFRYSPHLTELEQLLKRKGYLQLQQLLKYKRFPRAIALVEALAHRIPRDAEVRQWQAIVYQRYGRYSIECGQLDKARIYLKKALKTDPHNRSLWVEVERDFRRLERVL
>NZ_CP051167.1|WP_168570536.1|4688017_4688614_-|ATP-dependent-Clp-protease-proteolytic-subunit
MPIGVPKVPYRMPGETYTQWIDIYNRLYRERIIFIGKDIDDELANQVIAVMLYLDSEDSGKDIILYINSPGGMVTAGMAIYDTMQHIKSDVVTICVGLAASMGSFLLAAGTPGKRLALPHSRIMIHQPSGGTRGQASDIEIEAREIIRIRHQLNEIYARRTGQSLEKIEKDMDRDFFMSAYEAKEYGLVDRVIEDRTS

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Crispr_ID: NZ_CP051167_24

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_24

5132132-5132215

TypeV

N:A

Consensus_repeat	Method
CGGCGACACCTCGCACGGATTCGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051167_24

>merge|NZ_CP051167|24|5132132-5132215|CRISPRCasFinder
CGGCGACACCTCGCACGGATTCGGCGAATCGTCCAAATTCGGATCGATCTGGCAAATTCCCGGCGACACCTCGCACGGATTCGG

>NZ_CP051167|24|22|5132132-5132215|CRISPRCasFinder
CGGCGACACCTCGCACGGATTCGG	CGAATCGTCCAAATTCGGATCGATCTGGCAAATTCC
CGGCGACACCTCGCACGGATTCGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168570836.1\|5144761_5145610_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|370723
NZ_CP051167.1\|WP_168570838.1\|5146581_5147154_+\|PepSY-domain-containing-protein	unknown	unknown	gnl\|CDD\|377164
NZ_CP051167.1\|WP_168570827.1\|5129579_5130977_+\|argininosuccinate-lyase	unknown	unknown	gnl\|CDD\|179143
NZ_CP051167.1\|WP_168570822.1\|5122055_5122928_+\|glycosyltransferase-family-2-protein	unknown	unknown	gnl\|CDD\|133005
NZ_CP051167.1\|WP_168570821.1\|5121122_5121944_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|271381
NZ_CP051167.1\|WP_168570824.1\|5124425_5125055_+\|transcription-antitermination-protein-NusB	unknown	unknown	gnl\|CDD\|182007
NZ_CP051167.1\|WP_168570832.1\|5138401_5139826_+\|sugar-transferase	unknown	unknown	gnl\|CDD\|274398
NZ_CP051167.1\|WP_168570828.1\|5131387_5131942_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571988.1\|5137061_5137580_+\|thioredoxin-family-protein	unknown	unknown	gnl\|CDD\|379034
NZ_CP051167.1\|WP_168570820.1\|5119608_5120949_+\|DUF2064-domain-containing-protein	unknown	unknown	gnl\|CDD\|275103
NZ_CP051167.1\|WP_168570833.1\|5139950_5140952_-\|glycosyltransferase-family-9-protein	unknown	unknown	gnl\|CDD\|223928
NZ_CP051167.1\|WP_168570835.1\|5143800_5144478_+\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|223816
NZ_CP051167.1\|WP_168570823.1\|5123615_5124398_+\|DUF502-domain-containing-protein	unknown	unknown	gnl\|CDD\|225480
NZ_CP051167.1\|WP_168570834.1\|5141123_5141813_+\|2-C-methyl-D-erythritol-4-phosphate-cytidylyltransferase	unknown	unknown	gnl\|CDD\|234670
NZ_CP051167.1\|WP_168570837.1\|5145569_5145743_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570830.1\|5133388_5135683_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|226428
NZ_CP051167.1\|WP_168571987.1\|5129211_5129412_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570831.1\|5135923_5136634_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133055
NZ_CP051167.1\|WP_168570825.1\|5125444_5127070_+\|signal-recognition-particle-docking-protein-FtsY	unknown	unknown	gnl\|CDD\|236686
NZ_CP051167.1\|WP_168570826.1\|5127606_5129094_+\|PP2C-family-protein-serine/threonine-phosphatase	unknown	unknown	gnl\|CDD\|225118

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168570836.1\|5144761_5145610_+\|hypothetical-protein	gnl\|CDD\|370723	pfam09849, DUF2076, Uncharacterized protein conserved in bacteria (DUF2076). This domain, found in various hypothetical prokaryotic proteins, has no known function. The domain, however, is found in various periplasmic ligand-binding sensor proteins.	0.000512629
NZ_CP051167.1\|WP_168570827.1\|5129579_5130977_+\|argininosuccinate-lyase	gnl\|CDD\|179143	PRK00855, PRK00855, argininosuccinate lyase; Provisional.	0
NZ_CP051167.1\|WP_168570822.1\|5122055_5122928_+\|glycosyltransferase-family-2-protein	gnl\|CDD\|133005	cd02511, Beta4Glucosyltransferase, UDP-glucose LOS-beta-1,4 glucosyltransferase is required for biosynthesis of lipooligosaccharide. UDP-glucose: lipooligosaccharide (LOS) beta-1-4-glucosyltransferase catalyzes the addition of the first residue, glucose, of the lacto-N-neotetrase structure to HepI of the LOS inner core. LOS is the major constituent of the outer leaflet of the outer membrane of gram-positive bacteria. It consists of a short oligosaccharide chain of variable composition (alpha chain) attached to a branched inner core which is lined in turn to lipid A. Beta 1,4 glucosyltransferase is required to attach the alpha chain to the inner core.	5.09176e-78
NZ_CP051167.1\|WP_168570821.1\|5121122_5121944_+\|hypothetical-protein	gnl\|CDD\|271381	cd11490, SLC5sbd_SGLT6, Na(+)/chiro-inositol cotransporter SGLT6 and related proteins; solute-binding domain. Human SGLT6 (also called KST1, SMIT2) is a chiro-inositol transporter, which also transports myo-inositol. It is encoded by the SLC5A11 gene. Xenopus Na1-glucose cotransporter type 1 (SGLT-1)-like protein is predicted to contain 14 membrane-spanning regions. This subgroup belongs to the solute carrier 5 (SLC5) transporter family.	0.00872277
NZ_CP051167.1\|WP_168570824.1\|5124425_5125055_+\|transcription-antitermination-protein-NusB	gnl\|CDD\|182007	PRK09634, nusB, transcription antitermination protein NusB; Provisional.	2.20726e-102
NZ_CP051167.1\|WP_168570832.1\|5138401_5139826_+\|sugar-transferase	gnl\|CDD\|274398	TIGR03025, EPS_sugtrans, exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase. Members of this family are generally found near other genes involved in the biosynthesis of a variety of exopolysaccharides. These proteins consist of two fused domains, an N-terminal hydrophobic domain of generally low conservation and a highly conserved C-terminal sugar transferase domain (pfam02397). Characterized and partially characterized members of this subfamily include Salmonella WbaP (originally RfbP), E. coli WcaJ, Methylobacillus EpsB, Xanthomonas GumD, Vibrio CpsA, Erwinia AmsG, Group B Streptococcus CpsE (originally CpsD), and Streptococcus suis Cps2E. Each of these is believed to act in transferring the sugar from, for instance, UDP-glucose or UDP-galactose, to a lipid carrier such as undecaprenyl phosphate as the first (priming) step in the synthesis of an oligosaccharide "block". This function is encoded in the C-terminal domain. The liposaccharide is believed to be subsequently transferred through a "flippase" function from the cytoplasmic to the periplasmic face of the inner membrane by the N-terminal domain. Certain closely related transferase enzymes, such as Sinorhizobium ExoY and Lactococcus EpsD, lack the N-terminal domain and are not found by this model.	1.84751e-137
NZ_CP051167.1\|WP_168570835.1\|5143800_5144478_+\|response-regulator-transcription-factor	gnl\|CDD\|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	4.14347e-84
NZ_CP051167.1\|WP_168570830.1\|5133388_5135683_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|226428	COG3914, Spy, Predicted O-linked N-acetylglucosamine transferase, SPINDLY family [Posttranslational modification, protein turnover, chaperones].	7.42952e-50
NZ_CP051167.1\|WP_168570820.1\|5119608_5120949_+\|DUF2064-domain-containing-protein	gnl\|CDD\|275103	TIGR04283, glycosyl_transferase_family_2, transferase 2, rSAM/selenodomain-associated. This enzyme may transfer a nucleotide, or it sugar moiety, as part of a biosynthetic pathway. Other proposed members of the pathway include another transferase (TIGR04282), a phosphoesterase, and a radical SAM enzyme (TIGR04167) whose C-terminal domain (pfam12345) frequently contains a selenocysteine. [Unknown function, Enzymes of unknown specificity].	1.69333e-105
NZ_CP051167.1\|WP_168570833.1\|5139950_5140952_-\|glycosyltransferase-family-9-protein	gnl\|CDD\|223928	COG0859, RfaF, ADP-heptose:LPS heptosyltransferase [Cell envelope biogenesis, outer membrane].	4.02738e-57
NZ_CP051167.1\|WP_168570823.1\|5123615_5124398_+\|DUF502-domain-containing-protein	gnl\|CDD\|225480	COG2928, COG2928, Uncharacterized conserved protein [Function unknown].	1.10567e-77
NZ_CP051167.1\|WP_168570834.1\|5141123_5141813_+\|2-C-methyl-D-erythritol-4-phosphate-cytidylyltransferase	gnl\|CDD\|234670	PRK00155, ispD, D-ribitol-5-phosphate cytidylyltransferase.	1.73557e-111
NZ_CP051167.1\|WP_168570838.1\|5146581_5147154_+\|PepSY-domain-containing-protein	gnl\|CDD\|377164	pfam03929, PepSY_TM, PepSY-associated TM region. The PepSY_TM family is so named because it is an alignment of up to five transmembranes helices found in bacterial species some of which carry a nested PepSY domain, pfam03413.	0.00255404
NZ_CP051167.1\|WP_168571988.1\|5137061_5137580_+\|thioredoxin-family-protein	gnl\|CDD\|379034	pfam13098, Thioredoxin_2, Thioredoxin-like domain.	1.60117e-05
NZ_CP051167.1\|WP_168570831.1\|5135923_5136634_+\|glycosyltransferase	gnl\|CDD\|133055	cd06433, GT_2_WfgS_like, WfgS and WfeV are involved in O-antigen biosynthesis. Escherichia coli WfgS and Shigella dysenteriae WfeV are glycosyltransferase 2 family enzymes involved in O-antigen biosynthesis. GT-2 enzymes have GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	1.75597e-30
NZ_CP051167.1\|WP_168570825.1\|5125444_5127070_+\|signal-recognition-particle-docking-protein-FtsY	gnl\|CDD\|236686	PRK10416, PRK10416, signal recognition particle-docking protein FtsY; Provisional.	5.5071e-161
NZ_CP051167.1\|WP_168570826.1\|5127606_5129094_+\|PP2C-family-protein-serine/threonine-phosphatase	gnl\|CDD\|225118	COG2208, RsbU, Serine phosphatase RsbU, regulator of sigma subunit [Signal transduction mechanisms / Transcription].	8.75257e-89

>NZ_CP051167.1|WP_168570828.1|5131387_5131942_-|hypothetical-protein
MRDSHKRPSPSDAVLGGQNRVPRGAMVLGGVEGVRRRLSSPRVEHRIAALYEALNCGTDGLDLIIERLHDRSWKVRQAAYSILEKRTETQARQALRRYDSYNNCWQTWRSMGRLGGVDHVDTMMLALENDSNHATGKAIEESLDLVETIQGQNRLKDYLLNGTPIQRNYAASYFKKKGGLDFRV
>NZ_CP051167.1|WP_168570827.1|5129579_5130977_+|argininosuccinate-lyase
MSEQKTWSQRFESALHPAIARFNASIGFDIELIEYDITGSEAHAKMLAKTGIISSEEGEKLIQGLEQIRREYRQGLFKPGVDDEDVHFAVERRLTEIAGDVGKKLHTARSRNDQVGTDTRLYLREQVRHIRTQLVEFQQVLLDLAEANIETLIPGYTHLQRAQPLSLAHHLLAYVEMSARDWERLGDVYRRIDISPLGCGALAGTTFPIDRHYTANQLGFSRIYANSLDGVSDRDFAIEFLTAASLIMVHLSRLSEEVILWASEEFNFVTLKDSCSTGSSIMPQKKNPDVPELVRGKTGRVFGHLQGLLVLMKGLPLAYNKDLQEDKEALFDAVKTVRGCLEAMTILFREGLEFKGDRLAEAVASDFANATDVADYLAAKGVPFREAYNLVGKVVKMSLAAGKLLKDLTLDEWQQLHPAFEEDIYAAIAPKQVVAARNSYGGTGFEQVRQALVRARDRLNSASIE
>NZ_CP051167.1|WP_168571987.1|5129211_5129412_+|hypothetical-protein
MHWGEWLSVLNGSHFPDASVLAQQVNDPDILGRIQRTWMTFVKTGQIWAFIIGAILGYVFRGITGT
>NZ_CP051167.1|WP_168570826.1|5127606_5129094_+|PP2C-family-protein-serine/threonine-phosphatase
MTAVPFPRQPFGSTDSSANPNGSPTEVTPVLALKELVASLHREQNKVQDLLSSLGFALRSFNNLNQFLELIPLVASRVTDADGGALVLFKPNGQLRLQRLHCQEGQECQDIRQAIETATRQMSTPGGQNGSPTLPTATLDYQLSNYLGSDVHLFGTAILVKNSERGRLYVFSRDPDYTWTTTRQKLVRLVADQTAVAIENDELSVELRKKERLDRELEIGAEIQLRLLPRQCPHIEGIELAATCKTANRVGGDYYDFIPASHDLVGPKHNGGNPAERWSIAIGDVMGKGVPAGLIMTMTRGMLRAEVLNGHSPGRILQHLNRVMYNDLENSNRFVTLFYSEYDPKTRTLAYSNAAHNPPLLWRASTGQIDRLDTLGMLIGLDADTQYQEAQVQLNLGDTIMYYTDGFTDAVNQHGHRFDEENLVAAFEWACKHCHGPQAILDYLFDRVGEFIGPHNSNTDDMTLIVMQVRSPSETPEEEGVNPQTVDAEPSSTEE
>NZ_CP051167.1|WP_168570825.1|5125444_5127070_+|signal-recognition-particle-docking-protein-FtsY
MVFNWFRRQFDDRAQKSEAKTTESEPAQPEETTPSAEEESTDEEEVDYLTWAKAAYKNIQQQKGVSTEPEPEAEPEAVEAQSEPELEPEAVEAEAQPEPEAEPEAVEAQPEPETEPEAVEAQPEPEAEPEAVEAQPEPEAEPEAVEAQPEPEPEPAPTSFLARAEAERQSRLQRVAESAVEVVEEEEEFEESAAAREIWPTRHPELAFDEGFLWSAEVLAAQGRRPDEISVEEITWLQKLRQGLDKTRRSLINQLRAIVGQGPLNRDAVMEIEAALLQADVGIAATDYIIEALQEKMREEALPPDLAIAYLKRIIGDLLDRPTQELEKPFLVPEKDRLNIWLVTGVNGAGKTTTIGKIAHLAKKSDYKCLIAAADTFRAAAVEQMKVWGQRSGVEVIANPGKNTDPAAVVFDAIAAAQSRGTELLIVDTAGRLQNKKNLMDELSKIRRIINKKAPDAIVESLLVLDATLGQNGLNQAQVFSEAVNLSGAILTKLDGTAKGGIALAVVQQMNLPIRFIGAGEGIEDLRPFSSYEFVEALISG
>NZ_CP051167.1|WP_168570824.1|5124425_5125055_+|transcription-antitermination-protein-NusB
MQARRIARELALLSMSQLSNRPEKLSAQELEDLLLAAVRALTNEVHDILENAAAELKRGSDRLLNSELQATGVQSSRTMVYDAIELTQSAVNRLGMAMELPEFIQLTNRQEVRAYALEILSVIRDNRDRIDETIAASLVNWQLNRLPRIDRDILRVAVAEMFYIGTPDRVAINEAVELAKRYSGDDGHKFVNGVLRRVSDRAKEVSHKG
>NZ_CP051167.1|WP_168570823.1|5123615_5124398_+|DUF502-domain-containing-protein
MIQRFKQDLKNDLIAGLLVVIPLATTIWLTITIARWVIDFLTSIPKQLNPFDGLDPLLVYFLNLGVGLAVPLFSILLIGLMARNIAGRWLLDLGERLLQAIPLAGSVYKTLKQLLETLLKDSNEKFRRVVLVEYPRRGIWTMAFVTGALGASVQQQLNSHVPNGPMLSIFIPTTPNPTSGWYAIVPERDVVNLSMSVEDAFKAIVSGGIVNPNPSPPLPLPPSKQKKLDPLHAEQKPQEIATSDVPSELEDYSPEQEEYI
>NZ_CP051167.1|WP_168570822.1|5122055_5122928_+|glycosyltransferase-family-2-protein
MFSIYILTHNEQIDIAACIESAMLSDDIIVVDSVSSDRTVEIARQYPVRVVEHPFESHGKQRTWMLRSLETKYEWVYILEADERMTPELFEECVQAIEKSEAIGYYVAERVIFMDRWIKHCTQYPRYQMRLFRKDKVWFTDYGHTEREVCDGPTGFLKETYPHYTCSKGFSRWIEKHNRYSTDEAAETIAQLDRGQVSWRDLFGGRSEVERRRALKDLSLRLPWRPFLRFIYMYILLGGFLDGKPGFAWCTLQTFYEYLILLKVWERRHQPPVSAESASSSEGESLRPSP
>NZ_CP051167.1|WP_168570821.1|5121122_5121944_+|hypothetical-protein
MTPQSSIAAIALKVVGVVLILSSIIDYITLAIPVQLLERQWQLGYTTQIVDRGVIPLVALVFIFTGYWISSNEGGDRSSPGSIADLRFWALLFSTVLGVIYLLLFPLHLNNVRLERSATLTEIAQQANQAEEQLRGQLENPQFQQEIGQRREALKGQLSQLLEDQGRLDQALENPDVPDDEKQLLQEFKDNPGQIDAFLDERLSTEGFRDRRLTEIRTRRQDLESEAKTRFAKLAVQTGISSLLLSVAYSAIGWSGLKNMGYLQGGRRKRAGR
>NZ_CP051167.1|WP_168570820.1|5119608_5120949_+|DUF2064-domain-containing-protein
MISSPVRRDRLVIFTRYPQPGQTKTRLIPALGPEGAARLQRQMTELTCDRARQLRAAGVGDRRDLDIEICFTGGDRQGMQQWLGDDLLYKTQGDGDLGDRLARAVDRAFASGAERVVVVGIDCPHLETPILQQAFSALDRAPVVLGPALDGGYYAIAVRRPCPQLFEGIAWGSDKVFQQTIDKCSDLCIKPALLPPLADIDRPEDLDRLPDPLGRTLLAKISTIIPVLNEAERVRDTLASVTRGANVEAIVVDGGSRDDTPAIVESTGVRLLHSPPGRALQMNAGARAATGSILLFLHGDTRLPSGFETVIREILTRPGVVGGAFPLAIDSQQPGLKLLATVANWRSHLWQMPYGDQGLFVPREIFWDLGGFPELPIMEDYEFVRQLQRRGRIALAPTPVQTSARRWQQLGAFKTTAINQAIVLGYTLGVSPERLARWYRQSRDRP
>NZ_CP051167.1|WP_168570830.1|5133388_5135683_-|tetratricopeptide-repeat-protein
MNQSLNFYRDPLYLQALAADRAGYEQMALKNYRELLELYPKSADLWLELSRLYQRLQQYDRALEAIETSLNLSPNNANAYHQLSVSLSQLGYLQDAIAAGWKAIRLNSQSIETYLHLGYLLLERGEFEQSEHIYRRAIAIAPQHYQTYLNLGHLDLIRERTDEAIALFQKALQLKPRDPDIIYNLALALSATGQTNEAILYFAFAAYRRQQYNEAISYFCQYLDTQTGEIEAYQALANCYQALNRIEDCLNLYQTAIDLYPHSLDLYLNYLLSLQYFGQSDRAIAAIEQANPSFAASLILKLHKLRLLPILYRSQEQIKTCRNHFNQNLNQILFKIQTTSELRTKEALQAIGSGTNFYLQYQGQDDTKIQSKYGEIVHQIMKANYPQWGEKRLLPPLTQEGKIKIGYLSCCLQWHTVGMVFLGWLREASRDQFEIVCYDIGRKTDKFNELFRLYSDRFYQIPNNLEAIAAKITQDCLHILVFLDIGMYAPMTQLAGLRLAPIQCAAWGHPVTSGSPTMDYFISADLLEPEDAQKHYTETLIRLPNIGICYPKPTIPPLRRSRSEFGVEEEAIVYISCQSLFKYLPQYDWIFAETARQVERAQFIFFGHPSSAISQQFYNRLDRAFDRLGLKFANFGKILPRQSYANYWNLLSISDVALDTFGFTGFLTTLDSVALGLPIVTRSGSFMRSRQSAGILKRLDCMETIAADEQEYLEIAVRLGLNSDWRNSLAEKIKRNGVNLFGDRAGVAGLEQFYRDTVRENWVQ
>NZ_CP051167.1|WP_168570831.1|5135923_5136634_+|glycosyltransferase
MEDLIDVSAIVPCFNQGEFILDAIASIEASVEVNWELIIINDGSTEPLTLEVLQYLERHGYWVINQSNRGLAAARNRGIREASGRYILPVDADNKIRPDYMGLARDILDSSPEIGVVYGNVQFFGDRQALWHVPAFDRDRLLQSNYIDACAVFRKQLWEGCGGYDTAIPNRLGFEDWDLWLTALGRGWQFYRLPEIVFDYRVRPRSMVTRCLQQENHDKILEYLRKKHPDLLRGKQ
>NZ_CP051167.1|WP_168571988.1|5137061_5137580_+|thioredoxin-family-protein
MAVLLWFAGAPSARASLNDDRFDGNIYALYGGNGSLVPPKVTFRQALKRDDKATLVVFYLDDSRDCKQFASVVSQLQAYYGRAADILPLNVDAITTEGSFTPNDAGYYYEGVVPQTVVFDQSGKKVYSGLGQVDFGEVDRVLRKLYNLVPRDESQELKKRSFNEFNSELAPD
>NZ_CP051167.1|WP_168570832.1|5138401_5139826_+|sugar-transferase
MHKQKLDIRAPIIAQLSRGTGIGWLRVALLAIVDSLTIAAAWYLADLWGTPVGGFSLLWNVDGKPGFLLPIMAITIGILWASGLYGTDDRRRDFFSLIKSLTLAQGVLLIVGYLYEPEAVASRSTFLLAWIFNLLFVFSERLIIHLSIINLRHKGAIRQRISLLGQAPDIEEAQKLIQKTKQYIICDAEDVGLRQEEDWSSLIDKLRLKQVSEVFVCSHLSVKQQVSLYWELKTAGIHLRILPMGLELPIQWSEIKMVNGLPTMRFRSPPIIGGDFWIKRGFDLVAGSLILLATSPILTAIALAIKIDSPGPIFYKQTRIGVKGREFKVWKFRTMVVDAERLQKQLEEMNEMKGGIMFKMKEDPRITKVGRFLRRYSLDELPQIINVLIGEMSLVGPRPFPLRDVERFSEHHHMRHEVLPGITGLWQVSGRSDIIDFEDVFRLDMTYIQNWSVSLDFQILFQTIKVVLGKEGAY
>NZ_CP051167.1|WP_168570833.1|5139950_5140952_-|glycosyltransferase-family-9-protein
MRILALVPGGIGDQILFFPTLEDLKRSYPNARIDVIVEPRAKDAYRVCKFLHDKSLQVLPFDFVDRNGLADWGNLLGVVRDREYDAVISLERRPLFKVLLWLSGIPTRVGYRDLTFDDWFLNAAVERKTEQYLPLVNHDLLQGLGLNTPCPDLSVTLLKEDLNWAEAEQDRLGVKNSGYILAYGGSGSLCETQGSDGIYPVEQWQQIVEQIQQRQPQLPIVWIEEPENPELSQQLAGACPGLKVTSAPDLGKLAGMVAAANLMLCTDSVPLHLAVALQTYTIALFGPTTAKKRLPSPTDRGSDAEVRFLSIQSPTGKLADISPETVLDKVWGS
>NZ_CP051167.1|WP_168570834.1|5141123_5141813_+|2-C-methyl-D-erythritol-4-phosphate-cytidylyltransferase
MHLLIPAAGMGRRMGSDRNKLLLQLSNRPLLAWTLQAVNAAEQITWIGIVGQPTDWPDFKAILAAEPPSKPVEFIPGGDTRQESVYNGLQALPDGAERVLIHDGARALATPHLFDRCAESLRHCSGIVAAVPVKDTIKIVDPTDELIRDTPDRRNLWAAQTPQGFEVAALKDCHDRGRREGWQVTDDAALFEKNGLPVKIVPGEETNLKITTPVDLAIAEFILQQRLGS
>NZ_CP051167.1|WP_168570835.1|5143800_5144478_+|response-regulator-transcription-factor
MKILLVEDDNRIAETLASILRDRYYTVEIAGDGERAWSLASAFSYDLILLDVMLPKIDGITLTQRWRAAGKSTPILILTAKNTSRDKVLGLDVGADDYVVKPFDLPELLARIRALLRRGDRDPSLILKWGLLQLDPNRCESEYNGVALPLTPKEYSLLELLLRHPRRLFSRPAILDRLWSFEDPPGEETVKVHIRSLRKKLQAAGAPSNFIQTVYGLGYRLNQHL
>NZ_CP051167.1|WP_168570836.1|5144761_5145610_+|hypothetical-protein
MDDDFFDDDDFFENDFDDNLFDDDFDDDDFDDDDFDDDFFDRIDGFIDRLVQPRFYLTTYPDVAEAIRNGSFRGDADDHFEEFGGREGRDPSIFYSEQFYLANNPDVAEAVNRGQFLSGFEHFFSFGAREGRNPSPNFNSNFYLENNPDVAAAVNRGTFNSGFFHFIAFGQFENRQPRPASPPAPVANDPLIGSTANPAQFASDNADPLTTGGTIANEAIEIAPAVPGDRLPDLAAVSGGSAPEDLSLFLPNTVEGFAASTPALPTLSDVESNGDRLPLDLF
>NZ_CP051167.1|WP_168570837.1|5145569_5145743_+|hypothetical-protein
MNRTAIASPSICFSLIGGKPRTLREAVGMKAEAIEWNGLANLVNLNWHGSNALDGQD
>NZ_CP051167.1|WP_168570838.1|5146581_5147154_+|PepSY-domain-containing-protein
MNKAAFRKLHRTIAPIIFVPLLLSALTGIGYRIGRSWLAIPRRAGHLLMAVHQGEYLGHALTPVYVLFVGLGLLGAIATGLTLTGWFRGNRSAKAANSLNFRQIHRRLAPLFFIPLALVAMTGIGYCLGESWLGLPEGITDRLMDIHQGSFLGNRLRPIYVLVVGMGLLSLLITGIEMTGMFRKKRQSSM

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Crispr_ID: NZ_CP051167_25

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_25

5266046-5266141

Orphan

N:A

Consensus_repeat	Method
GCTCGAAAGCGGGCAAGATGCCCGCCCTAC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051167_25

>merge|NZ_CP051167|25|5266046-5266141|CRISPRCasFinder
GCTCGAAAGCGGGCAAGATGCCCGCCCTACAGATTTTGATTTAGGATGGATATAGTGTGCTTTTTTGCTCGAAAGTGGGCAAGATGCCCGCCCTAC

>NZ_CP051167|25|23|5266046-5266141|CRISPRCasFinder
GCTCGAAAGCGGGCAAGATGCCCGCCCTAC	AGATTTTGATTTAGGATGGATATAGTGTGCTTTTTT
GCTCGAAAGTGGGCAAGATGCCCGCCCTAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168571997.1\|5264770_5265901_+\|geranylgeranyl-reductase-family-protein	unknown	unknown	gnl\|CDD\|273936
NZ_CP051167.1\|WP_168570941.1\|5277284_5277491_+\|high-light-inducible-protein	unknown	unknown	gnl\|CDD\|177653
NZ_CP051167.1\|WP_168570930.1\|5261426_5261933_-\|single-stranded-DNA-binding-protein	unknown	unknown	gnl\|CDD\|223702
NZ_CP051167.1\|WP_168570925.1\|5247187_5248078_-\|phosphate/phosphite/phosphonate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270232
NZ_CP051167.1\|WP_168570938.1\|5272683_5272959_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570935.1\|5267627_5270456_+\|GAF-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP051167.1\|WP_168570934.1\|5266174_5266651_+\|NADAR-family-protein	unknown	unknown	gnl\|CDD\|225776
NZ_CP051167.1\|WP_168570939.1\|5273041_5273905_-\|fatty-acid-desaturase	unknown	unknown	gnl\|CDD\|366126
NZ_CP051167.1\|WP_168570940.1\|5274151_5275225_+\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270281
NZ_CP051167.1\|WP_168570928.1\|5255817_5257170_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|373105
NZ_CP051167.1\|WP_168571998.1\|5275437_5276949_+\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|226654
NZ_CP051167.1\|WP_168570926.1\|5249014_5250820_+\|mechanosensitive-ion-channel-family-protein	unknown	unknown	gnl\|CDD\|366370
NZ_CP051167.1\|WP_168570942.1\|5277553_5278051_+\|Orange-carotenoid-protein	unknown	unknown	gnl\|CDD\|370323
NZ_CP051167.1\|WP_168570927.1\|5250813_5255085_-\|PAS-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP051167.1\|WP_168570937.1\|5271727_5272687_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225779
NZ_CP051167.1\|WP_168570932.1\|5263211_5263940_+\|UMP-kinase	unknown	unknown	gnl\|CDD\|239787
NZ_CP051167.1\|WP_168570936.1\|5270416_5271592_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|132512
NZ_CP051167.1\|WP_168570933.1\|5263926_5264475_+\|ribosome-recycling-factor	unknown	unknown	gnl\|CDD\|178850
NZ_CP051167.1\|WP_168570929.1\|5257501_5261059_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238121
NZ_CP051167.1\|WP_168570931.1\|5262488_5263043_+\|thioredoxin-family-protein	unknown	unknown	gnl\|CDD\|239267

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168571997.1\|5264770_5265901_+\|geranylgeranyl-reductase-family-protein	gnl\|CDD\|273936	TIGR02032, Uncharacterized_protein_MJ1520, geranylgeranyl reductase family. This model represents a subfamily which includes geranylgeranyl reductases involved in chlorophyll and bacteriochlorophyll biosynthesis as well as other related enzymes which may also act on geranylgeranyl groups or related substrates. [Biosynthesis of cofactors, prosthetic groups, and carriers, Chlorophyll and bacteriochlorphyll].	7.86854e-82
NZ_CP051167.1\|WP_168570941.1\|5277284_5277491_+\|high-light-inducible-protein	gnl\|CDD\|177653	PLN00014, PLN00014, light-harvesting-like protein 3; Provisional.	4.97113e-07
NZ_CP051167.1\|WP_168570930.1\|5261426_5261933_-\|single-stranded-DNA-binding-protein	gnl\|CDD\|223702	COG0629, Ssb, Single-stranded DNA-binding protein [DNA replication, recombination, and repair].	3.93766e-21
NZ_CP051167.1\|WP_168570925.1\|5247187_5248078_-\|phosphate/phosphite/phosphonate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270232	cd01071, PBP2_PhnD_like, Substrate binding domain of phosphonate uptake system-like, a member of the type 2 periplasmic-binding fold superfamily. This family includes alkylphosphonate binding domain PhnD. These domains are found in PhnD-like proteins that are predicted to function as initial receptors in hypophosphite, phosphonate, or phosphate ABC transport in archaea and eubacteria. PhnD is the periplasmic binding component of an ABC-type phosphonate uptake system (PhnCDE) that recognizes and binds phosphonate. PhnD belongs to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. The PBP2 have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	8.26736e-58
NZ_CP051167.1\|WP_168570939.1\|5273041_5273905_-\|fatty-acid-desaturase	gnl\|CDD\|366126	pfam00487, FA_desaturase, Fatty acid desaturase.	9.81055e-16
NZ_CP051167.1\|WP_168570935.1\|5267627_5270456_+\|GAF-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.556e-45
NZ_CP051167.1\|WP_168570934.1\|5266174_5266651_+\|NADAR-family-protein	gnl\|CDD\|225776	COG3236, COG3236, Uncharacterized protein conserved in bacteria [Function unknown].	1.49093e-71
NZ_CP051167.1\|WP_168570940.1\|5274151_5275225_+\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|270281	cd13563, PBP2_SsuA_like_6, Putative substrate binding domain of sulfonate binding protein-like, a member of the type 2 periplasmic binding protein fold. This subfamily includes the periplasmic component of putative ABC-type sulfonate transport system similar to SsuA. These domains are found in eubacterial SsuA proteins that serve as initial receptors in the ABC transport of bicarbonate, nitrate, taurine, or a wide range of aliphatic sulfonates, while other closest homologs are involved in thiamine (vitamin B1) biosynthetic pathway and desulfurization (DszB). After binding the ligand, SsuA interacts with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The SsuA proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.76712e-52
NZ_CP051167.1\|WP_168570928.1\|5255817_5257170_+\|hypothetical-protein	gnl\|CDD\|373105	pfam14516, AAA_35, AAA-like domain. This family of proteins are part of the AAA superfamily.	0
NZ_CP051167.1\|WP_168571998.1\|5275437_5276949_+\|sensor-histidine-kinase	gnl\|CDD\|226654	COG4191, COG4191, Signal transduction histidine kinase regulating C4-dicarboxylate transport system [Signal transduction mechanisms].	7.77468e-48
NZ_CP051167.1\|WP_168570926.1\|5249014_5250820_+\|mechanosensitive-ion-channel-family-protein	gnl\|CDD\|366370	pfam00924, MS_channel, Mechanosensitive ion channel. Two members of this protein family of M. jannaschii have been functionally characterized. Both proteins form mechanosensitive (MS) ion channels upon reconstitution into liposomes and functional examination by the patch-clamp technique. Therefore this family are likely to also be MS channel proteins.	3.29804e-48
NZ_CP051167.1\|WP_168570942.1\|5277553_5278051_+\|Orange-carotenoid-protein	gnl\|CDD\|370323	pfam09150, Carot_N, Orange carotenoid protein, N-terminal. Members of this family adopt an alpha-helical structure consisting of two four-helix bundles. They are predominantly found in prokaryotic orange carotenoid protein, and carotenoid binding proteins.	4.29955e-84
NZ_CP051167.1\|WP_168570927.1\|5250813_5255085_-\|PAS-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	3.52096e-44
NZ_CP051167.1\|WP_168570937.1\|5271727_5272687_+\|hypothetical-protein	gnl\|CDD\|225779	COG3239, DesA, Fatty acid desaturase [Lipid metabolism].	4.53344e-14
NZ_CP051167.1\|WP_168570932.1\|5263211_5263940_+\|UMP-kinase	gnl\|CDD\|239787	cd04254, AAK_UMPK-PyrH-Ec, UMP kinase (UMPK)-Ec, the microbial/chloroplast uridine monophosphate kinase (uridylate kinase) enzyme that catalyzes UMP phosphorylation and plays a key role in pyrimidine nucleotide biosynthesis; regulation of this process is via feed-back control and via gene repression of carbamoyl phosphate synthetase (the first enzyme of the pyrimidine biosynthesis pathway). The UMP kinase of E. coli (Ec) is known to function as a homohexamer, with GTP and UTP being allosteric effectors. Like other related enzymes (carbamate kinase, aspartokinase, and N-acetylglutamate kinase) the E. coli and most bacterial and chloroplast UMPKs (this CD) have a conserved, N-terminal, lysine residue proposed to function in the catalysis of the phosphoryl group transfer, whereas most archaeal UMPKs appear to lack this residue and the Pyrococcus furiosus structure has an additional Mg ion bound to the ATP molecule which is proposed to function as the catalysis instead. Members of this CD belong to the Amino Acid Kinase Superfamily (AAK).	7.32072e-147
NZ_CP051167.1\|WP_168570936.1\|5270416_5271592_-\|glycosyltransferase	gnl\|CDD\|132512	TIGR03472, HpnI, hopanoid biosynthesis associated glycosyl transferase protein HpnI. This family of genes include a glycosyl transferase, group 2 domain (pfam00535) which are responsible, generally for the transfer of nucleotide-diphosphate sugars to substrates such as polysaccharides and lipids. The member of this clade from Acidithiobacillus ferrooxidans ATCC 23270 (AFE_0974) is found in the same locus as squalene-hopene cyclase (SHC, TIGR01507) and other genes associated with the biosynthesis of hopanoid natural products. Similarly, in Ralstonia eutropha JMP134 (Reut_B4902) this gene is adjacent to HpnAB, IspH and HpnH (TIGR03470), although SHC itself is elsewhere in the genome. Notably, this gene (here named HpnI) and three others form a conserved set (HpnIJKL) which occur in a subset of all genomes containing the SHC enzyme. This relationship was discerned using the method of partial phylogenetic profiling. This group includes Zymomonas mobilis, the organism where the initial hopanoid biosynthesis locus was described consisting of the genes HpnA-E and SHC (HpnF). Continuing past SHC are found a phosphorylase enzyme (ZMO0873, i.e. HpnG, TIGR03468) and another radical SAM enzyme (ZMO0874), HpnH. Although discontinuous in Z. mobilis, we continue the gene symbol sequence with HpnIJKL. Hopanoids are known to feature polar glycosyl head groups in many organisms.	6.0889e-47
NZ_CP051167.1\|WP_168570933.1\|5263926_5264475_+\|ribosome-recycling-factor	gnl\|CDD\|178850	PRK00083, frr, ribosome recycling factor; Reviewed.	1.18804e-104
NZ_CP051167.1\|WP_168570929.1\|5257501_5261059_+\|hypothetical-protein	gnl\|CDD\|238121	cd00200, WD40, WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from its N-terminus and the WD dipeptide at its C-terminus and is 40 residues long, hence the name WD40; between GH and WD lies a conserved core; serves as a stable propeller-like platform to which proteins can bind either stably or reversibly; forms a propeller-like structure with several blades where each blade is composed of a four-stranded anti-parallel b-sheet; instances with few detectable copies are hypothesized to form larger structures by dimerization; each WD40 sequence repeat forms the first three strands of one blade and the last strand in the next blade; the last C-terminal WD40 repeat completes the blade structure of the first WD40 repeat to create the closed ring propeller-structure; residues on the top and bottom surface of the propeller are proposed to coordinate interactions with other proteins and/or small ligands; 7 copies of the repeat are present in this alignment.	2.27178e-76
NZ_CP051167.1\|WP_168570931.1\|5262488_5263043_+\|thioredoxin-family-protein	gnl\|CDD\|239267	cd02969, PRX_like1, Peroxiredoxin (PRX)-like 1 family; hypothetical proteins that show sequence similarity to PRXs. Members of this group contain a conserved cysteine that aligns to the first cysteine in the CXXC motif of TRX. This does not correspond to the peroxidatic cysteine found in PRXs, which aligns to the second cysteine in the CXXC motif of TRX. In addition, these proteins do not contain the other two conserved residues of the catalytic triad of PRX. PRXs confer a protective antioxidant role in cells through their peroxidase activity in which hydrogen peroxide, peroxynitrate, and organic hydroperoxides are reduced and detoxified using reducing equivalents derived from either thioredoxin, glutathione, trypanothione and AhpF.	5.29666e-70

>NZ_CP051167.1|WP_168571997.1|5264770_5265901_+|geranylgeranyl-reductase-family-protein
MFDCIIVGGGPAGGTAAYHLAKRGRSVLVVEKEALPRYKPCGGGVSPAIAQWFDFDFSPAISLKVKQLRYTWQGGDPIDAEIETPEPMWMVRRDVFDNFLIEQAKAQGAQVRDNTEVTGVKFAGDRWTVTTNGEPVEGRYLIAADGAKGPMPKLLGFKERKPHTAWAIEVSGSESDDSARIQFDLGQVKKGFIWNFPKADGYSIGAAALQGRSKDNLDKTMQTYAGQLGLSLDGAKHYEHGLCLWDGEQKLHTQNALLAGEAACMVDPLTAEGIRPSMYSGMKAAEAIDGALGGDAKALETYTQVMNEEWGSDMTWAGRLAGVFYQFPGLAYKVVIKQPAATYRMGQILCGELRYGEIANKAIKHIKGSLIPGRGR
>NZ_CP051167.1|WP_168570933.1|5263926_5264475_+|ribosome-recycling-factor
MKLSEVESHMSKAVEATQRSFNTIRTGRANAALLDRVMVEYYGSPTPLKSLANISTPDASTIAIQPYDRSSLAAIEKAISMSDIGLTPNNDGSIVRLNIPPLTSDRRNEFVKLAGKYAEEGRVAIRNIRRDAIDSIRKQEKNSDISEDESRDLQDRIQKLTDKYTAKVDELLAAKEEDIKTV
>NZ_CP051167.1|WP_168570932.1|5263211_5263940_+|UMP-kinase
MGIVYRRVLLKLSGEALMGDLAYGIDPGVVQGIAEQVAEVTSKGVEVAIVVGGGNIFRGVKGAAAGMDRATADYIGMIATVMNAMTLQDALEQIGVPTRVQTAISMQEVAEPYIRRRAMRHLEKKRVVIFGAGSGNPFFTTDTTAALRAAEIDAEVIFKATKVDGVYDCDPHQNPEARRYESLTYGHVLANDLRVMDSTAIALCKENNIPIVVFDLTVKNNICRAVMGEKVGTIVGGYCEVI
>NZ_CP051167.1|WP_168570931.1|5262488_5263043_+|thioredoxin-family-protein
MENTGKSIGIHAPDFELPGIDDQVHHLARYLDRYRAVCTVFMCNHCPYVRGYLERLKQIQSQFEGRDFTLIGINSNDAVQYPEDGFEKMKSFAREHGLNFPYLRDANQDVAASFGAHLTPQVFLLDQSGVVGYSGAIDDSPDDPKAVGVHYLRDAIAQLLDGETIRIPSSQPVGCSLKWRQSPS
>NZ_CP051167.1|WP_168570930.1|5261426_5261933_-|single-stranded-DNA-binding-protein
MNSCILMAEIIEAPQLRYTNDNLAIAEMLVQFPALRSDDPPETLKVVGWGNRAEEIHNDFKLGDRVVLEGRLKMETREMPQGYKEKRAELTVQRVHRLDGSASQTAPAPTAARSPAPSNLVSMESRRPEPPVERSQPSRPAAPPPPTPRPTAPSFNDSDDDMDDEIPF
>NZ_CP051167.1|WP_168570929.1|5257501_5261059_+|hypothetical-protein
MSLYFYQVGGSLEPNSPNYVVRPADYQLYQALKQGDFCYLLNCRQMGKSSLLVRTSHRLQAEGYRCTSLDMSAIGSQLITAEQWYKGIVADLWRSFELFGKVNLKQWWQDKKDLSVSQQCKEFIEDILLKFFPDRNIVIFIDEIDSLLSLDFCVDDFFALIRFFFNQRAVNPEYKRLSFALFGVATPSDLIADRQRTPFNIGRAIALDGFTLEQAQHLALGFEGKTRDPEAILKAILGWTGGQPFLTQKLCYLARVALEYPADGEDSPALPLLPIAGKEREWIEFLVRDRLIYNWEEQDEPEHLKTIRNRLLVNFQSAARHLSLYQKLLENGDCELDDSREQIELLLSGIAVKQNGRLTVKNRIYREVFDRAWVKAQLDRLRPYASALDAWLATDREDRSRLLRGRALADARLWAQGKRLSDADYQFLAASEQFDREIVQQALEAQRVREVEGRLKEQHKRLALERENARRQRTFILVLSGVLAVAVALGVCALWQYREAISSERRSRVSAVQALVSSSQALFASERNLDALVEAIAAHQALDRLPSAPKPLQTEVQGVLQQALYSATEVNRFSGHLGWVLAVESSPDGRRVATGSNDRTVRLWKPDGTLLSTLPHGHTVHALAFSADSQSLVTSNLNGMVYTWDRDGRAIGNFRAHDSAIWDVAVSPDGKRIATASEDGTIALWSFQGQLLATLTGHQGAVWGVAFSPDGKLIASGSEDRTLRIWTADGKAATKIDAHEAAVWDVEFALLEVDGGEQKQTVISASADRTIGLWNPDGMAISTIEGHESEVFEIAVSADGKQIASASADKTVRLWTSQGMPLKVFKGHQSSIRGVTLLGSRGTIISASDDSTVRLWKPNRHFSQKIVAHRGTIWDIDYSPDGELVGTGSNDRTLKLWTRDGSLVRSLTTSEAAVLGIGFLPGKSASGVTWVASANSDRTIKVWQLDGTLVQTLAGHDGGVLDITPSPKGDRWVSASDDKTIKLWTRDGQLLKTLVGHQTRVYDVDFTPDARRLVSASEDGTIRVWSTDGELLKTIDAHQSGIWQVAVSPDGQRIASASLDDTIALWTIEGELVKTLEGSGMGITSIDWSADGRMLVSGGASGVVQLRDAEGNEIAVLKGHQGNVWGVAFSPDGKQIASVGDDRALILWDVERIVNLDPVAYGCDLIRDYLHTNSQLKEEQRQLCD
>NZ_CP051167.1|WP_168570928.1|5255817_5257170_+|hypothetical-protein
MTIDQVVQLLNASLSQPLTELQEWMLRRSWEGQTYADMAAQLNYSAQYLRSKAASELWPILSEFWGESISKPNLRSQLEACPLSREQQQLLETLNRTYPYELPNFPSGPVPLDSPLYIDRPPIEELAYQELTRPGTVIRIKAPRLMGKSSLMLRMADRARQLNYHIVKLDFQEADASIFNSSDRFLRWLSANVTRQLQLDLHLDDYWFEEIGSKVSCTSYFEEYLLSQIETPLLFILNEVNVVFEYPEIARDFLPLLRFWHEQAKQRENWTKLRLIVIYSTEVYIPLNVNQSPFNVGLPLSLPPFSLAQTQELARRHGLDWSNSKEAKELRDFVGGHPYLIRIALYYLCQSGQSLTLKQLLAEASSDTGIYGDRLRNLLLTLKQNPQLYDAFRKVISSDRPVLLEPIAAYKLDCLGLVRCSTDGCAISCELYRRYFEFHFRNLQFGSDSC
>NZ_CP051167.1|WP_168570927.1|5250813_5255085_-|PAS-domain-containing-protein
MTSSKETANPTIDVNVLLIDEHSSEQKAIATMLDRPYKNFQFTLWKCLTLSEAGFIITVEQFDIIFINLSGISETEIEAFSQCNCKNQGIPLVAIVDESQEEWAISLSESWLDEYIVKGRYDRDLLVRLIRWASCYHHLEHQTSRESNNKIFWQSYFNNPLVGFYKIRPNLGQIPGGEPWLDLNPSFCHWLNYSLGDLMFKSWDEFTHPEDVNQELEHLRQIYNSQKNIAIFNKRWLGKNGEIVHTRVCLSCSRDDHGEIEQLTATLVNISDRLRSEEILVEREQFLQSIYNGIEAAIAVVNVEENGEFRFLGINRMQEKLLGLRSREVEGKSPEDLFSPEIAKTVCERYKSCLRSVKQIVYEQSLLSEGEPSWWITNLTPLFDAENRIDRIISTSFNISDRKQAEEEVRASQHFIEQVAEANPNIIYIYDIEERRNVFINRNIAAMLGYNKAEIAAMGNTVLPTLMHPDDFARYPSYLEKIINGSDGEFFEIEYRMRSKSGTWYWLNSREVIFARTPDGNPKQILGTATNITELKHQAEELQIAGNRLQLALEGSNLGLWDWNLSTQEVYFDPYWKKMLGYEVEELQNSFETWEKLVHPDDLPPIRVRLMDYLENRLPSYNVEFRMKHKSGEWRWISCHGKIFDRDKNGKAVRMTGTHQDITDRKLAELELIKFQLAVESSSDAIGMADIEGNHYYHNQAFSDLYGYPTAAEFNAAGGPPIAFVDREIGKQVIETISSGRPWVGEVEQIARDGRKMQILLRANPIKDKQGNIVGLIGINTDITERKRVEEEKTELIQSLQQTTRHLQDAQRIAHIGNWELDIVSSEMMWSEELFRIFGLEPSSAVSFDDIINTRIHPDDRPALLTQIEQAIARGTCYNIDSRIIRNDGSIGYINSRGETLLDESGKAIKLMGTSIDITERKQAEESLKQQFVREQLTGAIANKIRQTLDLDAILNTTVFELQKVLKADRVLVYRIFPDETGCAIAEMTAPGIEKLLDRVFPEEVFPRDVYASYLQGRICAVGDRDAGGIVPCLVDFMVEIGVRAKLVVPIVQHQTLWGLLIAHDCSQPREWQTWEISLCKQLANQVAIGIQQSTLFKQAKSELVERKAAEYALRKSEARERAKAIELEQLVHQLKNTQAQLVQQEKMAGLGQMVAGIAHEINNPVNFIYGNLSHATDYTHDLLNLLELYRGSFPHPGSDILEEIEAIELDFLKEDFPNLLNSMREGANRIKGIVMSLRNFSRLDEAERKQADIHSGIDSTLMILHHRLKKQRERPEIEVIQEYGDLPLVECYPGQLNQVLMNVLTNAIDALEERMKSDCHLKPRICIQTRLGELKISDDRSENLPSVVIRIADNGNGITPQVQSHIFNPFFTTKEVGSGTGLGLSISYQIVVEKHRGKISCHSQVKQGTEFTIEIPMRYIGH
>NZ_CP051167.1|WP_168570926.1|5249014_5250820_+|mechanosensitive-ion-channel-family-protein
MSIHTARGGRPRVIRRSRRRSIAVAIAIFSFVFGAIVGIERAAIAQSAAGAAQIQSLFPPTSIVSENRIGNLVYAPVILDGRKLFRVAAAAVSDADPARGETSLLNERVDRIENELYGLIATGFNPETLQINVAILNGETAIVASDGDRVNNQPIVTVTDLDARIYGFSVSQWAQALSEIIHQGAIRAYRERQLPYLLRHAQIAAAIAVAVAVLTLGLQSLEKRLKATTIALPGPTPSLEAVDSLPSAFRPSSPEEVRAADRSRAIAQRQEVINRDRHRNLTSLKQWLLQIAKLLLWIGGIAAIAGLFPWTRWLQSWLASKPIVLVAIVLLTKLSIDVSCVLVDVFLNTLVQRTTLNSNGSQRQALRFSTFSVVLKSVAFFICATVGTVVALERLDIPLGPILAGAGILGFAISLSSQNFIKDVVNGCLILIEDQYAIGDFIAIDPVMGFVENMNLRVTQLRDGDGHLITIPNGTISIVRNMSKNWSRVNFTIQVAYDNDIEKVMQILEQVGQQLYEDPEWSDRIIEVPLLLGIDELAHQGITLRVWIKTAPLQQWAVGREYRRRLKLSFDRLGISIGIPQQYISFKTDTNGEVPFPRSSQ
>NZ_CP051167.1|WP_168570925.1|5247187_5248078_-|phosphate/phosphite/phosphonate-ABC-transporter-substrate-binding-protein
MKRRQFLWSSLLFVAGCTTATRQPERNRSQTAANCPDPLRLAITDIKGLEQLQAEFGAFKSALADVLGRNVEFFSVENYVAASPALLSGRVDLVLAGPSEYVLLHARAQAIPLIALTRPDYYSVISVRADSGIKSLKQLKGKTIAMRTAGSTAGHLGSTKLLVDVGLNPQSDFRTVMTGDRGLEALQNGEVDAWADSNIRRTQFLREAGLSESAVPIVARGTDLPSDVFAANSQLDPACLEEVRSLMLAAQDQLLKGILASAANEKYASSEMVAAKDSDYDPIREAYRAIGQDDYL
>NZ_CP051167.1|WP_168570934.1|5266174_5266651_+|NADAR-family-protein
MTIYFYKVPDPYGCFSNFSPHSIHLNGRDWPTVEHYYQAHKFVGTRDEGLIEKIRGVKTPEEAAALGRDRGYEVRSDWEGVKREIMYEAVLTKFLTHRDIQKVLLETGDEAIVEDSPTDYYWGCGAEKTGANHLGKILMEVRSQLRDRAVFTETIVGG
>NZ_CP051167.1|WP_168570935.1|5267627_5270456_+|GAF-domain-containing-protein
MKHTENHVRSLQQKLDREVLLHRTIDRIRQSLELEEILTATAAEIRSFLGTDRVMVYRFNPDSSGEVIAESIDEGRLCSLKGLNFPPDDIPLEARERFLQQRVRSIVKVNSQQIGLSPFGCNGREDPGEREQVEISYRPLDPCHMTYLKAMGVYCSLVVPIIANGELWGLIVSHHAEERDISEEDLQLVQLVTDQVSIAIAQATLLAKTRERQAREATINRIATLLHGSPEIELQGALEATVQSLDGCGGRVYIAPAEGDDDVRGRRLPEIFAWGDRPTFPDATETPILEEHPQWRQWRERRRSPSHNSSQVYERADAIADLYKDPSLAAIAPAFKNTQIRGLLVIPLYYRQKFLGYLSIFRHEVDTETLWAGRFNSNVRQLMPRQSFEAWRERKKNQAREWTDEELQMAKALGDQFSMGVGQYLLYKKVTALNANLEYQVQQRTAQLQNTLKFTRILKQVSDRIRSTLDLDEILQTIVGRVRNLLNTDRVVIYQFRGDGTGEVTVEDVRGNWKSVLGTRCPGDCFPQAYGNLYLRGRVRAIDDIATEDLTPCHREFLESLQVKANLIVPIRMGSDLWGLTIAHECQGPRVWSKDEIELVQQLGDQAAIAISQAELYRKSQQAAATAEAKARELTVALQDLQHAQGQLVQSEKMSSLGQLVAGVAHEINNPVNFIYGNLAHATEYAHDLLELLDLYQKHLPEPDVEIVDLMEDIDFEFLVEDLPRMLASMKVGADRIRQIVLSLRNFSRLDQSEMKPVNIHDGIDSTLMILHHRIKAKGDRPAIEIVKNYGDLPSVECYAGQLNQVFMNILGNAIDALEEAWIAHSHPDQPPGPTPSIRITTERHKNHTIAIEIRDNGPGIPEHLKNRIFDPFFTTKDIGKGTGMGLSISHQIVVEKHGGQFVCESEPGNGTTFRIVIPIAALRPSPGPTHPVGSRLSERSS
>NZ_CP051167.1|WP_168570936.1|5270416_5271592_-|glycosyltransferase
MLWNGIGIAIAVLASVTAWAMVVATLYFLRSRSIDRGESPAPPEVDSSVRVSILKPIKGLDDRLERNLEAFLNLQSIAYEVLIGIGDRRDPAWPAIDRFLAAHPEAPMRVIFTDSPPDAHPKMSNLAGLEAQACGEILLVSDGNTCPPPDALERLVASFADPQIGLVAAPFLVRSPLTLGARLRSLRIGTAIACSICGSYTLFKTPFVVGKWMAVRQQALAEMGGFAALSGVMCADGLIYPKLRALGWRGAIVPQAIDVYLGPWSWRQAWSQQLRWSRHVRFVAPIETAVEFLWNGLFLGSLAIAFAWGGATIAACALGAAGLGIWCAYAIAYVSLGGAATDLLLLPIVDLQMLAIAVWAYASNEIQWRGRRFYIGPGGQLERSESLDPTG
>NZ_CP051167.1|WP_168570937.1|5271727_5272687_+|hypothetical-protein
MNPTPLPPPAHLDLTPPERLNIALSCAIVLAGLGLQWGASHVGHAGIAFGFAIAFSFLFLPLYSLLHEAEHNLFHRHPKINNTFGFLLAAFFPGSFTFLRSCHLGHHRRNRTDAEMFDLYYPTDNLGMKRLYFYSLYLGLFWLAVPVATIALLIYPKLLQNQLLQDAPSASAMINGLPTHYLLKIRLECLAVIAIQVSLFFWLDLQLQWYLLLYACYGLNWSSQQYINHAHSPRHVLNGAHNLKAHGLYQGLLLNFNWHLAHHQYPNVPWIYLPQFDDINRDRPGYLTAFIRFWAGPQPCQEPEPKAIALPKIGREITS
>NZ_CP051167.1|WP_168570938.1|5272683_5272959_-|hypothetical-protein
MSTESEFLYPHSHFHGELTPENIEFHNKMEDFVQRSSILSNLASNGKISLEQAFTEIGDLWEELCQKKEQLNIGTSSEVSQTEPSEKEDRS
>NZ_CP051167.1|WP_168570939.1|5273041_5273905_-|fatty-acid-desaturase
MLTPTPIDGLRSPRDGRSLTFVAIAYLLLLVPFAIDLPIGCWGFWLIGSSLFCFCACVINHNHQHLPIFVRPWLNQVFNVILTPIRGHTATQIAIPHNYNHHIYHGDRRDWMSPELAGEGCGCVRWLRYLVKASLHTAHQRKQPDAPQLSPEQQQSLQRERVVLWLFIGAIAIANPVKALWFVGVPWGMAVIALLSVNFIQHDGCNPGDRYNCSRNFTSSLGNWLFFNNGYHTIHHLRPTLHWSELPEAHDRLVKPHLNPDLDVRSILGFFLSSYLLAWRSPKIKNP
>NZ_CP051167.1|WP_168570940.1|5274151_5275225_+|ABC-transporter-substrate-binding-protein
MQKFNHDRFGSSWAFLRNFNFKLRVKRRKFPLLLSILTLFCVIALNACLGSPQGELTPLRMGITPWPGFDIAIYGKEAGLFQQRGLDVEFVRFDNQQDSSRAVMRNQLDLAFASLWDVMQVDPTSDRPEFVMVTNVSQGSDGVVAKPGIESAKQLRGKKIGCKLGTVNHLILLEALQSNGIEPNAVEIADLPNEVAARQLKEGTLDAAVLWEPDLTAIAREIQGKVVFTTAEVDSLVIDGVIARSSFVAERERALQQFILAWFDIMNAVETQPDRVFEFVGEQLGQTGESFAQDYSGLQKGDRDLNRRMFATNGRLQEAVGKIAELLKADPRHGKSIREDIQLNATSVNAAIEAWES
>NZ_CP051167.1|WP_168571998.1|5275437_5276949_+|sensor-histidine-kinase
MLRRVVQNYVTLPAVREIAIVAPDGETITRSGAFKNDRPYALVRPQLAAAMEDSARSGEERFLELELDGKPVLVEILPFHNTLFGTSGRRGLAIAILDLRQLQAATLQMFLTLTGAIAIGIVAILILMWVSIHRVVLKPLTLVNQAVAESDRTGVFTMPANLPRNEIKFLARNFERVVKQLEAYDQLHKEIEQRKQVEAALRQSEARERAKSHELGKLVRELKQTQAQLVQTEKMSSLGRMVGGVAHEINNPVSFIFGNLTFAQEYFEQLVDLIELYQQSYPQPTPQIARRLDEIELEFLIDDTQKLFASMKVGAERIRDIVLSLRNFSRFDEAELKSVKIEEGLRNTLLILQPRFQGGSPVEIVTVEEFGDLPLVECYASQINQVFLNLLSNAIDALESDERYRHGRKLPVPATIWIRTEALNKKTIAVRIRDNGPGMPPEVRQKAFDPFFTTKEIGKGTGLGLSISYQIIVEQHKGRLECISKPGEGTEFVIEIPTQIPRS
>NZ_CP051167.1|WP_168570941.1|5277284_5277491_+|high-light-inducible-protein
MNGYTVNEQGLMNNFAVEPKMYVQEQSRTGFTQYAEKLNGRLAMLGFVSMLVMEALTGQGLISWLSNL
>NZ_CP051167.1|WP_168570942.1|5277553_5278051_+|Orange-carotenoid-protein
MAVTTEFNTAIFNPQLEAVPATLAEYERLSTDDKLGLLWVIYENLGGAITPAAPGAARMQFAEGLLNQIREMPFEAQLQAMRDLVEKVNNPISRAYGVLSNNNKLAFWFQLAEWMKSGEVIPVPANYSLSPRASAVFNRITLLDFNQQITVLRKAATDMGIDPFA

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Crispr_ID: NZ_CP051167_26

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_26

5352594-5352719

Orphan

N:A

Consensus_repeat	Method
TAAATTGGCGCCGGAGAGATCGGC	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP051167_26

>merge|NZ_CP051167|26|5352594-5352719|CRISPRCasFinder
TAAATTGGCGCCGGAGAGATCGGCACCGCGCAAGTTAGCCCGTAGCTGGGCATCCGCTAAATTGGCGCCGGAGAGATTGGCCCCGCTTAAATTCGCTTGGGACAGATCGGCGCCGGAGAGATCGGC

>NZ_CP051167|26|24|5352594-5352719|CRISPRCasFinder
TAAATTGGCGCCGGAGAGATCGGC	ACCGCGCAAGTTAGCCCGTAGCTGGGCATCCGC
TAAATTGGCGCCGGAGAGATTGGC	CCCGCTTAAATTCGCTTGGGA
CAGATCGGCGCCGGAGAGATCGGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168570988.1\|5341388_5343731_+\|DUF3488-domain-containing-protein	unknown	unknown	gnl\|CDD\|224224
NZ_CP051167.1\|WP_168570993.1\|5349835_5351230_+\|UDP-glucose/GDP-mannose-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|223936
NZ_CP051167.1\|WP_168570994.1\|5351307_5352075_-\|DUF2993-domain-containing-protein	unknown	unknown	gnl\|CDD\|378597
NZ_CP051167.1\|WP_168570992.1\|5348763_5349696_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|187541
NZ_CP051167.1\|WP_168571001.1\|5363065_5365114_+\|universal-stress-protein	unknown	unknown	gnl\|CDD\|223551
NZ_CP051167.1\|WP_168571003.1\|5365561_5366725_+\|DUF262-domain-containing-protein	unknown	unknown	gnl\|CDD\|377008
NZ_CP051167.1\|WP_168570999.1\|5359108_5361631_-\|phosphoenolpyruvate-synthase	unknown	unknown	gnl\|CDD\|235809
NZ_CP051167.1\|WP_168570996.1\|5354375_5354612_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168572002.1\|5338976_5340107_+\|heterocyst-differentiation-protein-HetZ	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570998.1\|5357548_5358805_-\|catalase	unknown	unknown	gnl\|CDD\|223824
NZ_CP051167.1\|WP_168570997.1\|5354883_5357073_-\|tetratricopeptide-repeat-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570990.1\|5346030_5346258_-\|type-II-toxin-antitoxin-system-CcdA-family-antitoxin	unknown	unknown	gnl\|CDD\|377822
NZ_CP051167.1\|WP_168572003.1\|5352842_5354246_-\|histidine-kinase	unknown	unknown	gnl\|CDD\|226701
NZ_CP051167.1\|WP_168570989.1\|5343816_5345676_-\|GAF-domain-containing-protein	unknown	unknown	gnl\|CDD\|236848
NZ_CP051167.1\|WP_168570991.1\|5346749_5348561_+\|elongation-factor-4	unknown	unknown	gnl\|CDD\|235462
NZ_CP051167.1\|WP_168571000.1\|5362380_5362965_+\|HD-domain-containing-protein	unknown	unknown	gnl\|CDD\|379122
NZ_CP051167.1\|WP_168570986.1\|5338389_5338881_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168570987.1\|5340151_5341285_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571004.1\|5366779_5367694_-\|histone-deacetylase	unknown	unknown	gnl\|CDD\|212518
NZ_CP051167.1\|WP_168571002.1\|5365319_5365520_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168570988.1\|5341388_5343731_+\|DUF3488-domain-containing-protein	gnl\|CDD\|224224	COG1305, COG1305, Transglutaminase-like enzymes, putative cysteine proteases [Amino acid transport and metabolism].	8.14701e-25
NZ_CP051167.1\|WP_168570993.1\|5349835_5351230_+\|UDP-glucose/GDP-mannose-dehydrogenase-family-protein	gnl\|CDD\|223936	COG1004, Ugd, Predicted UDP-glucose 6-dehydrogenase [Cell envelope biogenesis, outer membrane].	0
NZ_CP051167.1\|WP_168570992.1\|5348763_5349696_+\|SDR-family-oxidoreductase	gnl\|CDD\|187541	cd05230, UGD_SDR_e, UDP-glucuronate decarboxylase (UGD) and related proteins, extended (e) SDRs. UGD catalyzes the formation of UDP-xylose from UDP-glucuronate; it is an extended-SDR, and has the characteristic glycine-rich NAD-binding pattern, TGXXGXXG, and active site tetrad. 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.	0
NZ_CP051167.1\|WP_168571001.1\|5363065_5365114_+\|universal-stress-protein	gnl\|CDD\|223551	COG0475, KefB, Kef-type K+ transport systems, membrane components [Inorganic ion transport and metabolism].	1.53428e-57
NZ_CP051167.1\|WP_168571003.1\|5365561_5366725_+\|DUF262-domain-containing-protein	gnl\|CDD\|377008	pfam03235, DUF262, Protein of unknown function DUF262.	2.53925e-23
NZ_CP051167.1\|WP_168570999.1\|5359108_5361631_-\|phosphoenolpyruvate-synthase	gnl\|CDD\|235809	PRK06464, PRK06464, phosphoenolpyruvate synthase; Validated.	0
NZ_CP051167.1\|WP_168570990.1\|5346030_5346258_-\|type-II-toxin-antitoxin-system-CcdA-family-antitoxin	gnl\|CDD\|377822	pfam07362, CcdA, Post-segregation antitoxin CcdA. This family consists of several Enterobacterial post-segregation antitoxin CcdA proteins. The F plasmid-carried bacterial toxin, the CcdB protein, is known to act on DNA gyrase in two different ways. CcdB poisons the gyrase-DNA complex, blocking the passage of polymerases and leading to double-strand breakage of the DNA. Alternatively, in cells that overexpress CcdB, the A subunit of DNA gyrase (GyrA) has been found as an inactive complex with CcdB. Both poisoning and inactivation can be prevented and reversed in the presence of the F plasmid-encoded antidote, the CcdA protein.	0.00474824
NZ_CP051167.1\|WP_168570998.1\|5357548_5358805_-\|catalase	gnl\|CDD\|223824	COG0753, KatE, Catalase [Inorganic ion transport and metabolism].	0
NZ_CP051167.1\|WP_168571000.1\|5362380_5362965_+\|HD-domain-containing-protein	gnl\|CDD\|379122	pfam13328, HD_4, HD domain. HD domains are metal dependent phosphohydrolases.	3.23821e-33
NZ_CP051167.1\|WP_168572003.1\|5352842_5354246_-\|histidine-kinase	gnl\|CDD\|226701	COG4250, COG4250, Predicted sensor protein/domain [Signal transduction mechanisms].	7.60852e-55
NZ_CP051167.1\|WP_168570989.1\|5343816_5345676_-\|GAF-domain-containing-protein	gnl\|CDD\|236848	PRK11107, PRK11107, hybrid sensory histidine kinase BarA; Provisional.	7.52257e-60
NZ_CP051167.1\|WP_168570991.1\|5346749_5348561_+\|elongation-factor-4	gnl\|CDD\|235462	PRK05433, PRK05433, GTP-binding protein LepA; Provisional.	0
NZ_CP051167.1\|WP_168570994.1\|5351307_5352075_-\|DUF2993-domain-containing-protein	gnl\|CDD\|378597	pfam11209, DUF2993, Protein of unknown function (DUF2993). This family of proteins with unknown function appears to be restricted to Cyanobacteria.	7.52443e-21
NZ_CP051167.1\|WP_168571004.1\|5366779_5367694_-\|histone-deacetylase	gnl\|CDD\|212518	cd09992, HDAC_classII, Histone deacetylases and histone-like deacetylases, classII. Class II histone deacetylases are Zn-dependent enzymes that catalyze hydrolysis of N(6)-acetyl-lysine residues of histones (EC 3.5.1.98) and possibly other proteins to yield deacetylated histones/other proteins. This group includes animal HDAC4,5,6,7,8,9,10, fungal HOS3 and HDA1, plant HDA5 and HDA15 as well as other eukaryotes, archaeal and bacterial histone-like deacetylases. Eukaryotic deacetylases mostly use histones (H2, H3, H4) as substrates for deacetylation; however, non-histone substrates are known (for example, tubulin). Substrates for prokaryotic histone-like deacetylases are not known. Histone acetylation/deacetylation process is important for mediation of transcriptional regulation of many genes. Histone deacetylases usually act via association with DNA binding proteins to target specific chromatin regions. Interaction partners of class II deacetylases include 14-3-3 proteins, MEF2 family of transcriptional factors, CtBP, calmodulin (CaM), SMRT, N-CoR, BCL6, HP1alpha and SUMO. Histone deacetylases play a role in the regulation of cell cycle, cell differentiation and survival. Class II mammalian HDACs are differentially inhibited by structurally diverse compounds with known antitumor activities, thus presenting them as potential drug targets for human diseases resulting from aberrant acetylation.	2.18573e-135

>NZ_CP051167.1|WP_168570994.1|5351307_5352075_-|DUF2993-domain-containing-protein
MVSALFGSTPFQNQGGDALVSQVAGKAIAALFKRSEKVEANVRAEPVAKLLQGSIDGFDFIGQGMLMYNGLRIENMELYLQAVAIDFGAIFSGNVKLRQPTSARMRVVLTENDLTTSFNTPFVVEKLQRLQYNGESLHFQKTEVKLTSDKALRVSSEVKIGDADEPVHLDFTAQVDVEERRKVQFVNVKCEGSDRAVDLGNALIEHINSLLDLDKFALEGTQLRVDRIRIQSKAMVFYGSANIYQFPSRQLQKKS
>NZ_CP051167.1|WP_168570993.1|5349835_5351230_+|UDP-glucose/GDP-mannose-dehydrogenase-family-protein
MRVCVIGTGYVGLVTGACLAHTGHHVICVDNNEQKVKMMKAGQSPIYEPGLSDIIQKASQEDLLEFTTDLAYGVNHGDILFIAVGTPALPTGESDTRYVEAVARGIGSHLEKGYKVIVNKSTVPIGSGDWVRMIVLDGIAERQKASGGGNSISGDEAAAKLGIEFDVVSNPEFLREGSAVYDTFNPDRIVLGGNSDKALSMMEELYQPIVKRKFGEDPSLPPVPVVKTDLSSAEMIKYAANSFLATKISYINEIANICDRVGADVVQVAKGIGLDSRIGTKFLQAGIGWGGSCFPKDVSALIHTSDDYGYDAHLLKAAVDVNKRQRTIAIEKLQHELKILKGKTVGLLGLTFKPDTDDMRDAPALNLIEQLNRLGTKVKAYDPIVSQSGIGQGLSGVVVETSPEQLAYACDALVVVTDWQQFLTLDYAAMAKVMNNPVIIDGRNFLDRKMLQKAGFRYVGIGCS
>NZ_CP051167.1|WP_168570992.1|5348763_5349696_+|SDR-family-oxidoreductase
MRILVTGGAGFIGSHLIDRLMDQGHEVLCLDNFFTGHKHNILKWLDNPYFELIRHDITEPIRLEVDQIYHLACPASPVHYQYNPVKTIKTNVIGTLFMLGLAKRVKARFLLASTSEVYGDPDVHPQTEEYRGNVNTIGIRSCYDEGKRVAETLAFDYHRQNGVDIRVARIFNTYGPRMLENDGRVVSNFIVQALRGIPLTVYGDGSQTRSFCYVSDLVEGLIRLMNGESTGPINLGNPDEYTILELAEKIQKTVNPDAEIQFKPLPQDDPRQRQPDITKAKTFLGWQPTIPLDEGLKLTIEDFRSRLRSS
>NZ_CP051167.1|WP_168570991.1|5346749_5348561_+|elongation-factor-4
MTDVPVSRIRNFSIIAHIDHGKSTLADRLLMATGTVEDRVMKQQFLDNMDLERERGITIKLQAARMNYKGKDGQQYVLNLIDTPGHVDFSYEVSRSLVACEGALLVVDASQGVEAQTLANVYLALEHDLEIIPVLNKIDLPGAEPERVKAEIEEVIGLDCSQAILASAKEGIGIDEILESIVHLVPPPQDTIDRPLRALIFDSYYDPYRGVIVYFRVVDGTVKQGDRVRLMASKKEYEIDELGVLCPTQKPVDELHAGEVGYFAAAIKTVEDARVGDTITLAKAQASEALPGYTEAKPMVFCGMFPTDSDQFEDLREALEKLKLNDAALSYEPETSSAMGFGFRCGFLGLLHMEIVQERLEREYDLDLITTAPSVVYRVTTIDGEELLVDNPSNLPDPQEREKIEEPYVRVEMITPETYVGALMELSQSRRGEFKDMKYLTLGRTTLVYELPLAELVTDFFDQMKSRSRGYASMEYHPIGYRENPLVRMDILINSDPVDALSTIVHRDKAYPVGRALVEKLKELIPRHQFKVPLQAAIGSRVIASESIPALRKDVLAKCYGGDISRKKKLLQKQAKGKKRLKAIGTVDVPQDAFMAVLKLDRG
>NZ_CP051167.1|WP_168570990.1|5346030_5346258_-|type-II-toxin-antitoxin-system-CcdA-family-antitoxin
MNDQVVHSDRKEKVEVSIHLDAELLEQIQHLTNDPSKVIETAVRQWLRGERSRDNDLSRNLLRNPPVPPRGEWND
>NZ_CP051167.1|WP_168570989.1|5343816_5345676_-|GAF-domain-containing-protein
MASADRFSVSSNSASGPSHHSQQGDNWLEALGAPLAFTHDREGYYRAFYWERASECELDPQTLIGTRIDEQFQPVAIVPYGDRVRRVLSSGVPERFSYPFRYRDCYFLFDLTIAAIPDSDSEGQQVLVMGRTIPGVLSQCELPTNENPNNSHLLASGLNLHQKLLAEIVGSLRRTLPPGSELYQKLLAQMSRQIRRTLDLNTIARQTVKGLAEALGVSRCFICLYNSARNCVQVTAEYCPGDRPSLLGWDFLLEDYPDWQRALDSSDAIAVETLILPGCAPQAALIFATRYQDRPNALVCLCQEAIADGERQPDPDPEPDRTWGAAEIEFVRELGEQVGTAIAHATLYQELEQAREQAEAASKLKSQFLANTSHELRTPLNGMIGFLKLIMEGMAEDEEEEKQFIEEAYRSALHLLNLINDILDIAKIEAGKMHLDLNPVNLGELVSTVENHTRALVQQKNLTLQIQLPETEDEILLYGNYQRLLQVMLNIVGNAIKFTHEGGIEIRATIVKNKVEVRGLELPGVVQISVTDTGIGVSLDKQDKLFQSFSQVDSDRTRQYGGTGLGLAISQKLIEAMGGLVNFYSLGEGLGSTVTFVVPLYQEPAIVSLGSPDSLDLLS
>NZ_CP051167.1|WP_168570988.1|5341388_5343731_+|DUF3488-domain-containing-protein
MSHSSGIWHLFDFRGVRRLRQKLAALPPPVPEHSIALRVLVQTLVIVGIIATDIAAQTQMSLWAIPLSILGAVWSWYRRDKPDIPVKFVLAIAMLLVLGAFFNRLIRELNDTRVVLAELLIRIQIIHSFDIPRRKDLGYSMVIGLILLGVAGTLSQTLAFAPLLFIFLALALPTLVLDYRSRLGLTPLSRRGESRSKPRQTLWQRLSRDLSPKRLGVFLLVTVSLGLLVFALLPRFPGYQLQTFPVSSEIEFEGEFDGRSIVNPGYARNGRGDGEDLGEGEGGDEPGEMDSTFYYGFNSRINQNLRGQMEPKVVMRVRSQAPGFWRVLAFDRYTGKGWEISRNDDVRTLDRPGWSYQFLIPRDARSAGTGLAEISRVVQSYTVVSDLPNIIPALLEPRALYFPTREVALDPEGSLRSPLGLLEGLTYTVISEVPHRDRTALGNAPKNYPPSIRDYYLDVPASIRDRVRQLAQEILQTSPNPLDNPYEQTLYLAQYLKQNYSIPTDPFGLPFFDENEDLVESFLFEQQGGYPDHFSTVLTVMLRSIGIPARLAVGFGPGEFNPFTGLYVVRNTDAYAITEVCFPQYGWFGFDPIPGHELIPPSVEEYEPFGVLQMFWKWVAGWLPSPVTGLIQTVVSAAIGGILRFAAWLLRLFGRGWFGVVSGLVVFLSFGLLGWLGWKGWKWWHYRRFLAKLPPLESIYRQMVDTLAREGYPKNPAQTPFEYARQLPPHYPEERAAAIAEISQAYVRWRYGGRQENCDRLSQVLKRLQRLQKGDRPSAR
>NZ_CP051167.1|WP_168570987.1|5340151_5341285_+|hypothetical-protein
MESRDAEAFERIQHSKALQQQLLEWLLSENRHPVELSPPGTTDIDRPFDPLDSETFDDFLSGPGDIEAGIANPDESPLGGIRPHQPGEIPAVQDRYYALLKRRLQTEIQHHLPLFPWENEVLDYDAETSDWSVAQQVPDRLWTAQLEQLNLPVTLPPAVLTRIFEQCRRLVNSSVQEGLKLVRAVEDLFPEQTYTLHQLAGTLMVAGAPQRSTDAIDRLSQAAADFPETYEAASPTQQMVMSLLAAREIVGSLTLSVRAGDPPVQRQWLTGYGTLELNVEYTRRDTPEASRSDRPSTAATSQAPSCLRVAADLPCGGRLTLEKDRSQGSNCRSDAGSLSVEVQDPQPHEKYFLKVELDDPDSHPLIFTVYPLDNFRA
>NZ_CP051167.1|WP_168572002.1|5338976_5340107_+|heterocyst-differentiation-protein-HetZ
MAEIERGVEDIFELLFTELQQSTRASEANCREVSGRIAAEVERICQQSKRIQASGEVRTWAIALSRHRLQQCLNYYKLGSQAGRIDLHSTLSAIVYRYITPPQVQSSYQARLNLIEDFLQGFYLEALNAFRREAQLEATFSPSTLLELAEYMAFTERYGKRRIPLPGGRSQQLIVLRAQTFSQQQPPETIVDMEQAAEGASLDSDRTWNDSSVQQVREAMVDPDSLSAEDSLRETVIQELMTYLQNRDQQDCADYFALRLQDLPTAEIEAILGLTPRERDYLQQRFKYHLIRFALSHRWELVHEWLEADLDHNLGLSPSQWQTFQQKIGPEQVKLLELKQQNLPEAQIAQALGCTLNQVQKRWFKLLEVAWEIRNH
>NZ_CP051167.1|WP_168570986.1|5338389_5338881_-|hypothetical-protein
MDLNQQIQLLTENAPQDGKTPGIVAAIAPVLKSVAGQLRHREYYLLQSLDSRWVVTTLSNRAHPDVEKRAIYAFPSLKDATNHAIAPKDAGTIAVAVPVTHILFQMVAIDAVDSLVFFETPGDFSTGIEVSRETLQQSIRAELQKHLQKRSSPQESQLPPDLA
>NZ_CP051167.1|WP_168572003.1|5352842_5354246_-|histidine-kinase
MNPESTLNQLKAALPEGQLPSSYGVYFKNTLVALCHALEDHILQTSSDKSEVDPLVLATFQQGKWYLQEAERYRKIADRSRHILISAVSDSGFSTHETSQLDNVSLVDLDPEDSLVNEWNLVILAPSYQAIVLCHELDPDEYRPEDRPQVDTERKFYGLWTFDRAVVSQSTEILLDRLRPYNPDLIDRLKATQRQILECKDVPQTDMSGVVSRIVSYLQSSQQQIVAVNRQTRELWELEGQALKVSRNLNANKLQAFLRMAQRVDERDSANPVASLQVSALSETLGQLLDLPTLKLRRLRLAGLLFRIGLVSAPPEVFSTPASQLDDVTRSFWRDRARIGAQLLAAMPELTPVKEIVEHHLEYWDGSGQPDGLRGEEIPIEARILGLVAYFQELTQTRGDRSALTPQAALEQCQQRSETRFDPKAIETLGNVVRLAEMGLMQLPNRPSQLPNVWLEESPAPSTTVKS
>NZ_CP051167.1|WP_168570996.1|5354375_5354612_-|hypothetical-protein
MRYESYSKNPLCEKNARNFKTLLHEPISRSSFSDFELFLSGKVTPVQGLGGVQIEQWESEGWKSTYLWAGFTLPGEWR
>NZ_CP051167.1|WP_168570997.1|5354883_5357073_-|tetratricopeptide-repeat-protein
MKETASEAQQLFDRGVEFAGKNTIPDLVAAIEALEMARSLWSKTGDRDREVLTLLELGSLYKALGATTPARERYNEALTFYQERGDRLLEAFILAQIGSLYAEDAIQLKLDSLPYQVGFPEENESSLTLSGLGSTSEIEGNSPDEWDSKIEQEVERAREFYARSLEIYEELNNSSNPDRIAVRQAQAQTLKRMGMMFVQRRRFYPHFFMRYYHFYDNFYNFKPKNFLEQSLEIYQEIGDLQGEAFVLGQLMKLYRDDPVKSEQLFDRAITIYDDLESARGDRNTTILQAKAKLLNIAAQNTSRETRETALMFYDRALTLYQQIGDRHGEANTIFDLAQFYSEVDVLKSRTYYQKSLNLYAETGDLFSQAEVYKRLGGTYFNLKDWIKSLSFFEQELDTIDEIIRLYQKLNDEKLTLKFKYRKPIILLKIAFVSNQEGDREQEFQALSRAQTVYQQPKNIKRESNFLISIAQYHQWHNRPKQSQKAIDEAIALYRESGDLEGEVRFLRDRVQRFFGRNLIDDIEPVNSRKELLLTYDRIIAIYQQLGNKREEARSLANLAEFYFSSLTVVDNIELKHPENTELALSFYQKALNVSREISDPDVQKSDQSFQVYLLLAMAKIYYVLDRQEQCVETLKEIERTTSGLDDLYNLAVDATTYEEPLLAIDFYYKLLQASRDLKMNSDSEIRYEESLIFRSISEIYYYELNDLGRALRYFEKAYQLDGKNQNLEH
>NZ_CP051167.1|WP_168570998.1|5357548_5358805_-|catalase
MSDRNNLTTADGIPVGDNQNSLTAGSRGPVLMQDFHLQEKLAHFNRERIPERVVHAKGAGAFGTFTVTQDITQYSKAKLFSQVGKQTDVLVRFSTVGGEQGSADAERDPRGFAIKFYTEEGNWDLVGNNTFSLINANNERVWCKFHVKTLQGIQNMTAEEAARVRGEDPDRALRDLYKAIARGEYPQWRVSIQVMTEQQAAKHPDNPFDVTKVWKHADYPLIEVGILELNRNPENYFAQIEQAAFSPSAVVPGISFSPDKMLQARIMSYPDAHRYRLGANYQQLPVNEPKCPVMHYQRDGAMALGNNGGNSPNYEPNSYDDAPKQNPAYVEPSLPLGNVEAGHYDHREGNDDYTQAGDLFRLLSTDERRRLIDNIVGSLSQATEEIQKRQLCHFFRADANFGGAIASGLGLEVEMPTR
>NZ_CP051167.1|WP_168570999.1|5359108_5361631_-|phosphoenolpyruvate-synthase
MVSTAPEKTPQGSKETAFVLWFEEVGIADLALVGGKNSSLGEMIQQLASKGVSVPTGFATTAYAYRYFIEKAGLEEKLRKLFADLDLDDVNNLRERGKQARALVMNTPFPQDLQDAIAAAYLQLCKRYGGDSQFCERFGPDYQKVCEEYSSDTDVAVRSSATAEDLPDASFAGQQETYLNVHGVKGVLEACHKCFASLFTDRAISYRHQYAEKREDFDEFSVALSVGVQKMVRSDLATSGVMFSIDTETGFKNAALITAAYGLGENVVQGAVNPDEYFVFKPTLKEGKRPILEKRLGSKEIKMVYDLGGSKLTKNVPVPEPEREKFCISDEEILTLAKWACIIEDHYSQVRGKDTPMDIEWAKDGMTGELFIVQARPETVQSQKAGNVIRNFKLNGTSDVLARGRAVGEMIGQGKARVILDVHKIDQFKEGEVLVTNKTDPDWEPIMKKSSAIVTNQGGRTCHAAIIAREMGIPAIVGCGTATADIETGQEITVSCSEGEEGKVYSGLIPFEVQETKIDNLPRTKTKILMNVGNPEEAFGLSSIPCDGVGLARFEFIIANHIKAHPLALIHYDELEDESVKKEIAQLTALYPKNKPEFFVDKLAHGIGTIAAAFYPNPVVVRMSDFKSNEYANLLGGKQFEPKEENPMIGWRGASRYYDPKYEQAYGLECKALKRVRDEMGLTNVIPMIPFCRTPDEGRKVLETMEKYGLKRGENGLQVYVMCEIPSNVILADQYSEIFDGFSIGSNDLTQLTLGLDRDSALVAHIFDERNKAVKDMVQMVIEKAKKNGRKIGICGQAPSDYPEFARFLVELGIDSISLNPDSVMKTLLDIAKLEESLNR
>NZ_CP051167.1|WP_168571000.1|5362380_5362965_+|HD-domain-containing-protein
MLSKRFNEALSFAAELHATQTRKGSGIPYIAHLLAVASIALEYGANEDEAIAALLHDAIEDQGGAIAREQIRRRFGDTVTAIVEGCTDADTLPKPPWRQRKETYLAHLLSASPSVRLVCAADKLHNARSILNDYRQVGEDLWTRFKGGRDGTLWYYRSLVETFKQIDSTPLIEDLARVVDELETTCKNPVRLSS
>NZ_CP051167.1|WP_168571001.1|5363065_5365114_+|universal-stress-protein
MEIVRDLFAQDPIFPFALLLGIILVVPLCFERLQLPGLVGLLVAGVVFGPHGLQLLESGSEAMKLLSDIGVVYLMFVAGLEMDIAQFQRVRDRALGFGFLTFLFPLIAGTIVGRWFGFDWNASILLGSLLSSHTPLGYPILSRMGLMGNEAVIVALGGTIFTNIPALLVLAICVGVKTGNFTPVELLILIVSLSLYSAVVLWGVNWVGKEFFRRSGDEEGNQFLFILLAVFVAAVGAQVIGVEKIIGAFLAGMAVNEVVESETVKEKVVFVGSVLFIPMFIINLGLLIDLQEFAKGLASFGLTIAIVGALLGSKWIAAVGTQWLYRYTRAETIAIWSLSIPQVAATLAATIVGYRQGILTEEVLNSAIVMMLVTATLGPWVTARVAGALPLPEADLGAIATTFDETEAQVGHLFTVVVPVCNPETERYLVEMAALLARSEAGQIVSLSIARSIAYMEVSALDEAIARGERLANEAVEFARSMGVSARGILRIDSDVALGIVHGSREQNASAIVMGWSETTSLRSRLFGNAIDSVLWGAHCPVAVTRLLASPMQMQRILVLVDRAIAQSVLSVRVAFILASANQGEVTLLYAGDRHTSPEVHEQIGAQLSQLVAQWSGSTPSQIAILADDDPVGAIVTASARYDLAILRSTRRRTVAGLEIDDLTTQLLRQLPLSLVMLGEPE
>NZ_CP051167.1|WP_168571002.1|5365319_5365520_-|hypothetical-protein
MREISSSVELFDSRRWRSSLVERVEPFIIHQFNSYIILGFEFEIETRETLQKLHGDRLDEIKLREI
>NZ_CP051167.1|WP_168571003.1|5365561_5366725_+|DUF262-domain-containing-protein
MIETGLTIANADTNSEEEAVLVEEKFDAEEDEDSPELEIPLSDRKLVTHPYDFVIRSLKDQIDDGTLILADKFQRRQVWDRTKSSRLIESLLLNVPIPVCYFAELEDGTYSVIDGQQRLTAIYRFLHDEYPLRALKVLSELNRQKFYQLDAPYKRLLLSRTIRCIVILKESHPDIKYDVFERLNSGFVPLNAQELRNSVYRGKLNDLIHQLSEDEVFQKARRVSDIDKRMHDCEMILRFFAFHFHLSEYKGTLARFLDRYLESGINFDEETLEQHRALFRQTIDDVYYVFEDRAFRRYTLENGWEKSLNRAIYDVVMLFFARLNSEDIRAMKDEIVEALKQVCQDPEFCEAITSSTKNKDRIQMRLDKWREALLNIGLDVPYLQVGQ
>NZ_CP051167.1|WP_168571004.1|5366779_5367694_-|histone-deacetylase
MFSAIYCDEFLLHDTGRGHPERPDRLRAIVKALKSAPWADRLHWQQPTPPNERAVSEAIARIHTRRHVHAVETIAHNGGGGLDLDTPVSPRSYEVAELAVSAWLDGIDWICQTGDPAFVLARPPGHHATPDRGMGFCLFSNAAIAAYYAIEQCGVERVGILDWDVHHGNGTQEIVETHPQMTYCSLHQFPCYPGTGRAEETGSYNNVLNIPMKPGSTGAEYKQAFDEKIMPFFENFKPDILIVSAGYDGNSSDPLAGIDLQPEDFGVFTNYCLQLTRRIVFGLEGGYELDSLSRSVLATIAPCL

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Crispr_ID: NZ_CP051167_27

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_27

5600459-5600559

TypeV

N:A

Consensus_repeat	Method
GAACCGACTCCAGGCGATCGCCA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051167_27

>merge|NZ_CP051167|27|5600459-5600559|CRISPRCasFinder
GAACCGACTCCAGGCGATCGCCACCGAACCCAACAAAACCCCAACTCAACCGCACCTCCGTTGTCCCCTACGTTATCTGGACCGACTCCAGGCGATCGCCA

>NZ_CP051167|27|25|5600459-5600559|CRISPRCasFinder
GAACCGACTCCAGGCGATCGCCA	CCGAACCCAACAAAACCCCAACTCAACCGCACCTCCGTTGTCCCCTACGTTATCT
GGACCGACTCCAGGCGATCGCCA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168572024.1\|5608500_5608902_+\|HNH-endonuclease	unknown	unknown	gnl\|CDD\|224321
NZ_CP051167.1\|WP_168571166.1\|5609360_5609543_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|273632
NZ_CP051167.1\|WP_168571160.1\|5598579_5600025_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224588
NZ_CP051167.1\|WP_168571167.1\|5609661_5610060_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571157.1\|5595877_5596888_+\|ParM/StbA-family-protein	unknown	unknown	gnl\|CDD\|212669
NZ_CP051167.1\|WP_168567325.1\|5603253_5603424_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571156.1\|5595348_5595531_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571161.1\|5601100_5601427_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571159.1\|5597495_5598593_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571152.1\|5593515_5593872_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571155.1\|5595058_5595352_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168572025.1\|5610073_5612935_-\|RHS-repeat-protein	unknown	unknown	gnl\|CDD\|225750
NZ_CP051167.1\|WP_015152084.1\|5596887_5597103_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571154.1\|5594651_5595059_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571153.1\|5593997_5594225_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|226181
NZ_CP051167.1\|WP_168571158.1\|5597099_5597387_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571165.1\|5607610_5608330_+\|recombinase-family-protein	unknown	unknown	gnl\|CDD\|214861
NZ_CP051167.1\|WP_168571162.1\|5602006_5602867_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571163.1\|5603456_5606483_-\|Tn3-family-transposase	unknown	unknown	gnl\|CDD\|376561
NZ_CP051167.1\|WP_168571164.1\|5606585_5607233_+\|recombinase-family-protein	unknown	unknown	gnl\|CDD\|214861

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168572025.1\|5610073_5612935_-\|RHS-repeat-protein	gnl\|CDD\|225750	COG3209, RhsA, Rhs family protein [Cell envelope biogenesis, outer membrane].	7.3811e-24
NZ_CP051167.1\|WP_168571166.1\|5609360_5609543_+\|hypothetical-protein	gnl\|CDD\|273632	TIGR01448, recD_rel, helicase, putative, RecD/TraA family. This model describes a family similar to RecD, the exodeoxyribonuclease V alpha chain of TIGR01447. Members of this family, however, are not found in a context of RecB and RecC and are longer by about 200 amino acids at the amino end. Chlamydia muridarum has both a member of this family and a RecD. [Unknown function, Enzymes of unknown specificity].	3.7195e-10
NZ_CP051167.1\|WP_168571160.1\|5598579_5600025_+\|hypothetical-protein	gnl\|CDD\|224588	COG1674, FtsK, DNA segregation ATPase FtsK/SpoIIIE and related proteins [Cell division and chromosome partitioning].	2.06895e-06
NZ_CP051167.1\|WP_168571153.1\|5593997_5594225_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|226181	COG3655, COG3655, Predicted transcriptional regulator [Transcription].	1.81302e-10
NZ_CP051167.1\|WP_168571157.1\|5595877_5596888_+\|ParM/StbA-family-protein	gnl\|CDD\|212669	cd10227, ParM_like, Plasmid segregation protein ParM and similar proteins. ParM is a plasmid-encoded bacterial homolog of actin, which polymerizes into filaments similar to F-actin, and plays a vital role in plasmid segregation. ParM filaments segregate plasmids paired at midcell into the individual daughter cells. This subfamily also contains Thermoplasma acidophilum Ta0583, an active ATPase at physiological temperatures, which has a propensity to form filaments.	8.96112e-34
NZ_CP051167.1\|WP_168571165.1\|5607610_5608330_+\|recombinase-family-protein	gnl\|CDD\|214861	smart00857, Resolvase, Resolvase, N terminal domain. The N-terminal domain of the resolvase family contains the active site and the dimer interface. The extended arm at the C-terminus of this domain connects to the C-terminal helix-turn-helix domain of resolvase.	1.68218e-39
NZ_CP051167.1\|WP_168571163.1\|5603456_5606483_-\|Tn3-family-transposase	gnl\|CDD\|376561	pfam01526, DDE_Tnp_Tn3, Tn3 transposase DDE domain. This family includes transposases of Tn3, Tn21, Tn1721, Tn2501, Tn3926 transposons from E-coli. The specific binding of the Tn3 transposase to DNA has been demonstrated. Sequence analysis has suggested that the invariant triad of Asp689, Asp765, Glu895 (numbering as in Tn3) may correspond to the D-D-35-E motif previously implicated in the catalysis of numerous transposases.	0
NZ_CP051167.1\|WP_168572024.1\|5608500_5608902_+\|HNH-endonuclease	gnl\|CDD\|224321	COG1403, McrA, Restriction endonuclease [Defense mechanisms].	2.73368e-11
NZ_CP051167.1\|WP_168571164.1\|5606585_5607233_+\|recombinase-family-protein	gnl\|CDD\|214861	smart00857, Resolvase, Resolvase, N terminal domain. The N-terminal domain of the resolvase family contains the active site and the dimer interface. The extended arm at the C-terminus of this domain connects to the C-terminal helix-turn-helix domain of resolvase.	7.02297e-36

>NZ_CP051167.1|WP_168571160.1|5598579_5600025_+|hypothetical-protein
MSRTKPDPLTTRQLGLLLAATLFSGSIAAWIASLTPQTTSAVRQTQGAIDVLTERTPNDNWGFFLGTSIACLAGGSLILSRKEFFDPSTLRDDAISTILALTSHSNYLLAGGLQATAKIALTSPPAKKGKEVVLRVIPPQLKSAAEKLSGDRKWFVEWAGFRKGLGGQSWQCNFVVGLPGSGKTTVVNEIIVGFIRFSEGTGQLRIFDINYGKPDDSGRVNTWMGLPLNQIVEAQFDRIHAGINAVWDELEKRRQQAIKVASDGGKQTLNFTPLLCVIDELPALMNTAKQHEVDEEIKEKIADILTMGRGYRVKLLLISQMLAVGSVALTKAQQQQVNKLILGTSALDADIINRIPGTAQDLRGEIEPLLKQKKRACVVQFGASLPEVRVIPEIDIKAHRVRVCATDPDEVWWRETWTGETRKRVEELARSYANGEIKSPLKGEVISLFNITNMSRDERYKRFVSPVWNELVNQHKTEQKP
>NZ_CP051167.1|WP_168571159.1|5597495_5598593_+|hypothetical-protein
MMTPFGGSYLEIEEDLPDLQDSPDETSNLPDLLNPPPLEADPAPTVKPSVNHARLWLIIGTIGVGLAVSAIAQNQPQFSQISLPQLNPQTGQQTHQKPICREGEQSMAGCIPLPALDPAEMRRNELLAKTLIETSMQQTAIDRARRDNLLALFAPNHKEGDYTPLDIKLVREMARQSQNLRELGQFEYSGEASIIDIPRVYNSDARAVVLAALTRIGEQSLVQSFLAQQLQTLTNELNEILAPTMGEVTDSNRATFERLSSEIDAVNDAIRASAGGNTPEPINLAYLASLMEQLTLESANQLSREDYMRLRMEARQQAITEEMERQKQLQEIERIRQQSGIALPSRSRSVSERESPTGGPPDEPN
>NZ_CP051167.1|WP_168571158.1|5597099_5597387_+|hypothetical-protein
MNYKITTLITCIVGSMLTMILVLGALEPQVDSARMMTIAILCGIGSAIANIVFQRRRCPPASDSLQSLLRGGRLSPAQQFTILDAIAILDEREKA
>NZ_CP051167.1|WP_015152084.1|5596887_5597103_+|hypothetical-protein
MGKKLTLRTELIPLVESFASAKGDDSLGAAMNRLIYLGLKAEGFIPHATHTKGGNTSPNNDDLEILGVIDL
>NZ_CP051167.1|WP_168571157.1|5595877_5596888_+|ParM/StbA-family-protein
MQPYALDLGNGYTKFSRGSTPQMMPSYICEALDPSELCDDIGFGAIIKYTVGERTDLAGRIWAVGEAAKTSFPGAFSRVVDSENSTGKVDFALHFALAGLPPVSHGQYFQIPMMYASLPDPALLGSAFKRAIIGTHRYIHNGVEASATIDDVTVLHEGQGAFVYALSQGVFPSGTANAIIDCGNGTTIAQAFSPNGHLIPKSRTVSQVGVFHLLKSIASDIRFKKTLGKEGNIHLIQQAIEDGSLSYGSRNIDISNIYREHRNRWASQALKKALEKFSTMKDEIDTILLIGGGANIVKILAEKKDSIELCPEPQLANVLGLAKLADKRIRNLRSVA
>NZ_CP051167.1|WP_168571156.1|5595348_5595531_+|hypothetical-protein
MNNVEERTIHWESVLMATPLPGELVTYVATILVQDENWGFDARTRQQQAIMARAAQSVSL
>NZ_CP051167.1|WP_168571155.1|5595058_5595352_+|hypothetical-protein
MQLPNKLAPFIQLDNLCYEDKLDLLIVATQALKQCHSNSHYEIDLLNALENSDCTQDAFEGITESHEFLEVTLTEVEWIQFSQAVLTALKLVFEVAK
>NZ_CP051167.1|WP_168571154.1|5594651_5595059_+|hypothetical-protein
MTTLSISSPKCMGFYSQGLQDKLYPFVENGQRLTLDDAIRLIHLSSEGAWWAMQKGMDQAIGQIMSDLEADSMDCVPFDGFDSDADEFRALKLELTEWLALARWSSELAELRLNDYTRAKVSEMAAQSPPIWEVL
>NZ_CP051167.1|WP_168571153.1|5593997_5594225_-|helix-turn-helix-domain-containing-protein
MMATVMEIYWNLRALMALKRVSVGELAEILEVSRTTASRYKNSDIVPPGLDHEKLTRLCELLQCEPGDLIKTAND
>NZ_CP051167.1|WP_168571152.1|5593515_5593872_-|hypothetical-protein
MVWSAPRDHHHPTGQLQRVAASPDRAIAAIQLALLWTKIFHRESPGAIVRLAPSCCIYANTAANRDPLSAKFSETERDRYLLALFRDGDFSGNGVQSEVVRLADGLTIALEKAQENLQ
>NZ_CP051167.1|WP_168571161.1|5601100_5601427_+|hypothetical-protein
MNTVAPFLNTYLKHRGVRMFSGDRFRTYKRGQYLVLEYRDGSGTLIIGRPTGNGSWETPKQFPVKVKREDANYIVERSIPLMQEDIRQRQQRYRPSKRSRSNQLDISD
>NZ_CP051167.1|WP_168571162.1|5602006_5602867_-|hypothetical-protein
MSRPSKKAEAKSSKSGRAQVNVRTTPQLLAQIDQARQDTSRSEFIVQAIEAYLGIEPPSPQTTATVQSLVDAAVEQAILGVTRTLEERLKALEIRLSASDVDENVDAPVDGLDAPGDSGDAPVDEVARVDVDGQVDSLVDSGDAPVEGEIQATSAELELEEVTVRDRHASPESERFVEAAGDSGDDAVEGEVQATSGELGLEEATGGDLSRSQESKQGVDAAGDFRTQGLSGRELAKRLSVSPSSITTNRKKKGTNAFAKWTSQQDPEEIAWSYQKERYYPVEPKG
>NZ_CP051167.1|WP_168567325.1|5603253_5603424_-|hypothetical-protein
MLFKPRLPLCDEDLDARESNRLNNRINELEEKIGMALAELRLRLTELEEENERLQD
>NZ_CP051167.1|WP_168571163.1|5603456_5606483_-|Tn3-family-transposase
MSIRFLTEEQQQSYGRYVGDPTPVQLARYFHLDDTARQLVNKRRGDHNRLGFAIQLCTVRFLGTFLTNPIDVPQVVIADLAAQLDITNKNCLPRYLERPTTHWEHAQAIKLHYAYRDFSEQPFHWRLVRWLYERAWVSDESPSILFDLTTARLVENKILLPGVSVLVRLISSVRERVAKRLWLLLSKLPNAEQTNQLEALLFVNEKMRPTLLEQLRRSPTRTSSSALVNALNRLVTIRSLGIRQLPVAKIPPTQLKALSRTALTVRAQAIARMPSSRRLATLVAFAYVMEAIATDDALDVLELLVKDLLSCSAREGKKERLRTLKDLDAAALQLSQVGRVLLDPNCDDEKVREKVWRLLTKDQLTKAVTQVEELARPPDHNYYQELLGRWRQARCFLPTLLLTIEFLANKAGQPILAAWRFLQSIEGQTKPDMKAAPLQVVSKSWGRWVVLSDGRIDRRAYTFCVLEQLVEGLRRRDLFVSPSERWSNPQAKLLQGRAWESARSHVCRALNLNPTPVEELNVLRQQLDEAYSRTANNLPNNAAVRIEVTKGRETLTISNLDKLEEPDSYLLLKQQVESLLPHVDLPEVLLEIQVKTGFMDEFIHINESFARVRDLSTSICAVLIASACNIGLTPLVRPDLPALTRSRLTWVEQNYIRPETLVRANARLVDTQAQIPLAQNWGGGEVASADGLRFVVPVRTLNAGPNSKYFGQGRGITYYNFTSDQFTGFHGLVVPGTLRDSLVVLVGLLEQQTSLQPKELMTDTSGYSDVVFGLFWLLGYQFSPRLADVGEARFWRLDTNADYGVLDKLARQWVKTHLIEQNWDDLLRVAGSLKLGTVSAQEIMRALQLGKKPSTLAKAIGELGRVAKTLYLLNYVDDEAYRRRILTQLNRGEGRHSLSRAIFYGRRGEVRQRYREGQEEQLSALGLVVNVLVLWNTYYMNTALNHLRLQGTLVKAEDIARLSPLAYSHINMLGRYHFNLPSELLDGGMRPLRDLNDFPETWGETPCM
>NZ_CP051167.1|WP_168571164.1|5606585_5607233_+|recombinase-family-protein
MVQKVAIYCRVSTSDQSCSRQERDLVAYAELAGYQVVGIWKETASGSKHRLLQRDQILKLAQARAIDAVLVTELTRWGRSTLDLIHTLQDLAHWRVSLIAQTGIEFSLDTPQGKLIANVMATLAEFERDLVRERVRSGLAAAKARGVKLGRQPGQRVKADRLENKVLLLVEQGHSYRAIARQLHLSKTTVNDIVKRHRQKTAPSLTGISTEDSES
>NZ_CP051167.1|WP_168571165.1|5607610_5608330_+|recombinase-family-protein
MTKGFDNSTVIYIRVSTDEQAKEGVSIPAQVEKLTAYCKQAGLRVVSTIIDDGVSAGKFLSTRPGGSQLVELVRSRQVKNIVAVKLDRLFRSAADALTSVDNWDKLGASLHLLDFNGMSLDTSSPMGRMMLTMIAGFAELERNLCKQRTKDAIQHKKASKQKYCRSVYGYQTLEDGTMVPDASEQEAICIIKMMRSSGASLRAICSKLTELGYKTKRGGVQWYAATIKGILENDIHQLA
>NZ_CP051167.1|WP_168572024.1|5608500_5608902_+|HNH-endonuclease
MSNRNWVFATKGEQPKKLVLHTEFATSSNKHLLVKGDRSPYEGDLVYWSRRLGRHPELPNRQAILLKQQQGKCAWWGLHFLSGNVMEVDHKIPLSQGEKDEWVNRQLLHRHCHDEKTAADGSQKSVIDKGIAH
>NZ_CP051167.1|WP_168571166.1|5609360_5609543_+|hypothetical-protein
MLGIERYLGDGQIPGIGPGLAKKIVAYFEEQTLSVIENQVERLIEVPGIGKKKADQIQAV
>NZ_CP051167.1|WP_168571167.1|5609661_5610060_-|hypothetical-protein
MKREFMLFWFNSKKKLEEFLQRPRMTDEDFLSELGFSGTKLKKVVKDYRSKLGDMFQVPPEKIYPNDKFGELSRLQPCDWDLLEIVLFLEDSLKVELDDEKVPDWNGTTNVGSWVADLLSKCFTQNRENLES
>NZ_CP051167.1|WP_168572025.1|5610073_5612935_-|RHS-repeat-protein
MYPDNTPENPNDNPRTINVYDKGGRQRATIDEAGRVIHYKYDAAGQLTETIYLDKTDTLQQFIDAVAPGKTAATIDWSLVVYPDDLPTYLTDNPRSVTEYNKNGQVKANIDQRGNRTEYRYDDAGRLIETIYPDDTPDDLSDNPRSKSEYNNAGQRVKEIDAQGHATRFVYDNLGRLVATHFADGTKAETIYDALGRRVAAIDQAENKTEYEYDALGRLTDVVQFLNGEEIRTEYGYDESGRLIWQEDANNHRTNYEYDNLGRRTAVELPDTQRSTTEYDAVGNTFSVTDFNGDTITYNYDAQNRLIEKRVGETPIASFTYTPTGQLETITDSRGVTSYSYDELGRLLSRTDPDGPYLTSGASIEYGYDSAGNRTSVTTPTGTIEYAFEEQNRLKTVTDDAGVTSYSYDEVGNLIRTELPNGVVETRTYDELSRLESVSYVKDGTLIASYDYTLDPVGHRRVVEERDGRKVEYEYDDLYRLTKEAIADPVNGNRTIEYTYDAVGNRLSRIDSVEGTTTYVYDESDRLVRKELTLDGNVVRVYEYRYDDNGNTIERIEKDGSNNVIGNATYSWDKENRLVGATTSTGDVISYSYDTDNIRVSSTVNGVTTEYLVDKNRPYAEVLSEYVDDTLAVSYLHGLDLISQERDGSESFYLVDGLGSTRLLTDEGGEVTNAYSYDAFGNLVASSGSIENEFLFAGEQYDESLEQYYLRQRYYDAGIGRFTRRDTYEGRLNEPITLHKYLYGNANPVNYVDPSGFFALTEVLAGSTIIGSLAGAVGGGYYGAYKSGEVFSKETLKFALVGAVGGAAAGAMLGGAFYLTPAGLGPILTRGFQELWRKALTRHSTTAAALIGGFALGFTGGLLEPDYEVTLGTALTTAITIVDDALIRGAIWRRHEIARVVGQGFATQAKVLLKYGQSTTFIALGFLFGFTIGYASGARIRKTYDHQYGLTNN

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Click the colored protein region to show detailed information

Crispr_ID: NZ_CP051167_28

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051167_28

5637229-5637323

Orphan

N:A

Consensus_repeat	Method
GATTCAGTTTCTTCAGGAATTGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051167_28

>merge|NZ_CP051167|28|5637229-5637323|CRISPRCasFinder
GATTCAGTTTCTTCAGGAATTGAAGTGAATTCAGTCGGCTCAACTGTTGTCTCATCAGATAGGAGAGTTTCTGATTCAGTTTCTTCGGGAATTGA

>NZ_CP051167|28|26|5637229-5637323|CRISPRCasFinder
GATTCAGTTTCTTCAGGAATTGA	AGTGAATTCAGTCGGCTCAACTGTTGTCTCATCAGATAGGAGAGTTTCT
GATTCAGTTTCTTCGGGAATTGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051167.1\|WP_168571177.1\|5636688_5636925_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571176.1\|5632865_5636444_-\|DUF4114-domain-containing-protein	unknown	unknown	gnl\|CDD\|275156
NZ_CP051167.1\|WP_168571184.1\|5649719_5650523_-\|DUF2993-domain-containing-protein	unknown	unknown	gnl\|CDD\|378597
NZ_CP051167.1\|WP_168571816.1\|5631863_5632901_+\|IS630-family-transposase	unknown	unknown	gnl\|CDD\|315923
NZ_CP051167.1\|WP_168571186.1\|5653239_5653674_+\|DUF4079-domain-containing-protein	unknown	unknown	gnl\|CDD\|372553
NZ_CP051167.1\|WP_168572026.1\|5652712_5653105_+\|DUF1830-domain-containing-protein	unknown	unknown	gnl\|CDD\|370162
NZ_CP051167.1\|WP_168571182.1\|5647479_5648820_-\|AAA-family-ATPase	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571180.1\|5639386_5639710_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571173.1\|5622169_5622556_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051167.1\|WP_168571183.1\|5648991_5649702_-\|thiaminase-II	unknown	unknown	gnl\|CDD\|381701
NZ_CP051167.1\|WP_168571172.1\|5620476_5622153_-\|DNA/RNA-non-specific-endonuclease	unknown	unknown	gnl\|CDD\|214889
NZ_CP051167.1\|WP_168571816.1\|5640107_5641145_+\|IS630-family-transposase	unknown	unknown	gnl\|CDD\|315923
NZ_CP051167.1\|WP_168571181.1\|5642260_5647162_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|280546
NZ_CP051167.1\|WP_168571175.1\|5626352_5631329_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|380078
NZ_CP051167.1\|WP_168571171.1\|5619817_5620273_+\|pentapeptide-repeat-containing-protein	unknown	unknown	gnl\|CDD\|224276
NZ_CP051167.1\|WP_168571816.1\|5622611_5623649_+\|IS630-family-transposase	unknown	unknown	gnl\|CDD\|315923
NZ_CP051167.1\|WP_168571174.1\|5623608_5626452_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225926
NZ_CP051167.1\|WP_168571185.1\|5650644_5652315_-\|B12-binding-domain-containing-radical-SAM-protein	unknown	unknown	gnl\|CDD\|223963
NZ_CP051167.1\|WP_168571170.1\|5615720_5619653_-\|RHS-repeat-protein	unknown	unknown	gnl\|CDD\|225750
NZ_CP051167.1\|WP_168571179.1\|5637547_5638417_-\|DUF4114-domain-containing-protein	unknown	unknown	gnl\|CDD\|379190

Protein	Function_ID	Function_description	E-value
NZ_CP051167.1\|WP_168571170.1\|5615720_5619653_-\|RHS-repeat-protein	gnl\|CDD\|225750	COG3209, RhsA, Rhs family protein [Cell envelope biogenesis, outer membrane].	1.06826e-23
NZ_CP051167.1\|WP_168571176.1\|5632865_5636444_-\|DUF4114-domain-containing-protein	gnl\|CDD\|275156	TIGR04362, hypothetical_protein, choice-of-anchor C domain. This family describes an extracellular bacterial domain that occurs on a number of proteins with PEP-CTERM (exosortase recognition site) sequences at the C-terminus, as well some with an apparent alternate anchor sequence. Note that related pfam04862 (DUF642), as of release 26, is double the length of this model because it has two tandem regions homologous to this domain. pfam04862, in turn, belongs to a Pfam clan called the galactose-binding domain-like superfamily.	4.27253e-27
NZ_CP051167.1\|WP_168571184.1\|5649719_5650523_-\|DUF2993-domain-containing-protein	gnl\|CDD\|378597	pfam11209, DUF2993, Protein of unknown function (DUF2993). This family of proteins with unknown function appears to be restricted to Cyanobacteria.	2.98562e-15
NZ_CP051167.1\|WP_168571816.1\|5631863_5632901_+\|IS630-family-transposase	gnl\|CDD\|315923	pfam13358, DDE_3, DDE superfamily endonuclease. This family of proteins are related to pfam00665 and are probably endonucleases of the DDE superfamily. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction.	6.61756e-30
NZ_CP051167.1\|WP_168571186.1\|5653239_5653674_+\|DUF4079-domain-containing-protein	gnl\|CDD\|372553	pfam13301, DUF4079, Protein of unknown function (DUF4079). This is an uncharacterized family of proteins.	1.35502e-29
NZ_CP051167.1\|WP_168572026.1\|5652712_5653105_+\|DUF1830-domain-containing-protein	gnl\|CDD\|370162	pfam08865, DUF1830, Domain of unknown function (DUF1830). This family of short proteins is functionally uncharacterized.	1.56024e-43
NZ_CP051167.1\|WP_168571185.1\|5650644_5652315_-\|B12-binding-domain-containing-radical-SAM-protein	gnl\|CDD\|223963	COG1032, COG1032, Fe-S oxidoreductase [Energy production and conversion].	1.36826e-59
NZ_CP051167.1\|WP_168571183.1\|5648991_5649702_-\|thiaminase-II	gnl\|CDD\|381701	cd19366, TenA_C_BhTenA-like, TenA_C proteins similar to Bacillus halodurans TenA. This family of TenA proteins belongs to the TenA_C class as it has a conserved active site Cys residue; the double Glu residues identified in the active site of TenA_E from the archaeon Pyrococcus furiosus is conserved in this family. TenA_C proteins (EC 3.5.99.2) catalyze the hydrolysis of the thiamin breakdown product 4-amino-5-amino-methyl-2-methylpyrimidine (amino-HMP) to 4-amino-5-hydroxymethyl-2-methylpyrimidine (HMP) in a thiamin salvage pathway. This family includes Bacillus halodurans TenA which participates in a salvage pathway where the thiamine degradation product 2-methyl-4-formylamino-5-aminomethylpyrimidine (formylamino-HMP) is hydrolyzed first to amino-HMP by the YlmB protein, and the amino-HMP is then hydrolyzed by TenA to produce HMP. It has also been suggested that TenA proteins act as transcriptional regulators based on changes in gene-expression patterns when TenA is overexpressed in Bacillus subtilis, however this effect may be indirect.	2.5361e-93
NZ_CP051167.1\|WP_168571172.1\|5620476_5622153_-\|DNA/RNA-non-specific-endonuclease	gnl\|CDD\|214889	smart00892, Endonuclease_NS, DNA/RNA non-specific endonuclease. A family of bacterial and eukaryotic endonucleases share the following characteristics: they act on both DNA and RNA, cleave double-stranded and single-stranded nucleic acids and require a divalent ion such as magnesium for their activity. An histidine has been shown to be essential for the activity of the Serratia marcescens nuclease. This residue is located in a conserved region which also contains an aspartic acid residue that could be implicated in the binding of the divalent ion.	4.48906e-22
NZ_CP051167.1\|WP_168571181.1\|5642260_5647162_-\|hypothetical-protein	gnl\|CDD\|280546	pfam02399, Herpes_ori_bp, Origin of replication binding protein. This Pfam family represents the herpesvirus origin of replication binding protein, probably involved in DNA replication.	8.11658e-05
NZ_CP051167.1\|WP_168571175.1\|5626352_5631329_-\|hypothetical-protein	gnl\|CDD\|380078	pfam17963, Big_9, Bacterial Ig domain. This entry represents a wide variety of bacterial Ig domains.	9.68891e-08
NZ_CP051167.1\|WP_168571171.1\|5619817_5620273_+\|pentapeptide-repeat-containing-protein	gnl\|CDD\|224276	COG1357, COG1357, Pentapeptide repeats containing protein [Function unknown].	1.16226e-13
NZ_CP051167.1\|WP_168571816.1\|5622611_5623649_+\|IS630-family-transposase	gnl\|CDD\|315923	pfam13358, DDE_3, DDE superfamily endonuclease. This family of proteins are related to pfam00665 and are probably endonucleases of the DDE superfamily. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction.	6.61756e-30
NZ_CP051167.1\|WP_168571174.1\|5623608_5626452_-\|hypothetical-protein	gnl\|CDD\|225926	COG3391, COG3391, Uncharacterized conserved protein [Function unknown].	0.00366038
NZ_CP051167.1\|WP_168571816.1\|5640107_5641145_+\|IS630-family-transposase	gnl\|CDD\|315923	pfam13358, DDE_3, DDE superfamily endonuclease. This family of proteins are related to pfam00665 and are probably endonucleases of the DDE superfamily. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction.	6.61756e-30
NZ_CP051167.1\|WP_168571179.1\|5637547_5638417_-\|DUF4114-domain-containing-protein	gnl\|CDD\|379190	pfam13448, DUF4114, Domain of unknown function (DUF4114). This is a repeated domain that is found towards the C-terminal of many different types of bacterial proteins. There are highly conserved glutamate and aspartate residues suggesting that this domain might carry enzymic activity.	6.85474e-20

>NZ_CP051167.1|WP_168571177.1|5636688_5636925_+|hypothetical-protein
MNSVEADEVVEATKSSSAKSRGSSSSELKSVSSVVKDEEFVSVESSEDSSESGVSSALAGVVAESDEAGDSASISSSD
>NZ_CP051167.1|WP_168571176.1|5632865_5636444_-|DUF4114-domain-containing-protein
MGETGSINIEYIFDGGYYQGTVGLFNMAGLSEYEWGSAEFFQEIARRSLSNSDEGYVLISDSTEAAKLDGKLEAYNWNRGIKSGEKTFSLPEGTEFGLILIPDGTLQELFDNPQVTGSKKPFLSLTPSDPERALHQPQLVDVTGDGNLFAWEDLRLPGGDADFNDITFKMSAATGIVTNLDEVIAPDSDWRNSEIGQQIVSYAEQNNQSPIITAKLAEDTGISDSDRKTYNPTITGTLTNPLHIVSFTASFDNSSFINIDSQLLETGDFTLTPSQLATIYGDSLPDGSHTLYLQAIDEWGNITEYQYDFTLDTTAPPLTFDLDPASDTDIPGDAQTAASPVTLTGTTEPNATVTLIETGTTVTADTTGQFSFAGIDLTVGENSFTIQTLDDAGNSTVTSRIITRTEVSNVDDIVLVEGENFSVSHREELTIPQTSSQLVFTLAALNFDRSDSNAINDAFEVALLDAEGNSLVHTIGSGDAFFNLTEGEEPKLAAGVEYNESTGTVTLNLNGVSPGSANLVLRLVNGDRDTTTSVSIRNLNLVGSTQQQPPVSSGEDNHRSQPIELAEFGKLTDITPSNPLEYRSTRFDESSNELYAEVAIRNEGNYSVDGPLLVAVSNISDPTVLLRNPDGFTPEGVPYYNFSELAEDGKLDPTEITELGSLTFFNPNRVQFTYELAVLGQLNADPVIESKPPLEAIGGNSYRYEVIAKDANNDGLSYSLLSAPNGMIIDSETGVITWETTVEEIGTHAVVVEVVDSRGGKDVQSFTLSVTEIPPNRPPIFTSTPVVDAYINQPYRYQISATDPDRDKLTFSVMNAPEGMSFDSETQTLTWQPNTQQLGLQKVTLNAEDGRGGKVTQSFNILIQEKPGNYAPIIISEPSQRVNVGSDYLYSVRALDPENDQLTYSLVNPPDGMTVDPITGEIRWNDLTDDNVGEYEIAVEVQDTQGGIDTQIFQLSVAHQTDLGEIRGIKWLDSNKNSVFDPEESGLAGVEIYLDLNNNGRLDVEEPSTKTSTDNPATPLTDETGSYQFTNLTADTYTIREIVPSSLEQTFPLLSPAIGENLIQNGSFERGPAPKNSWTIVRYNSTTLEGWDVMLRSVDHCGTGLWQASDGDYSIDLDGTPGPGGIKQTINTIPGEDYLVTFDLSAHGFLAAGSERPMTVTAAGQSAEFVGIGSGNKNIAILSHLWQKSIRI
>NZ_CP051167.1|WP_168571816.1|5631863_5632901_+|IS630-family-transposase
MNIIDELDNFIENTTNTKEMKRALAAKMKLSGQPSKKIEEILNVSSSFVSQWKNKAIFEGVESLNLQYKGSKGYLKPEEKTQITSWIRQQEYLRLSDLKRYLQQEYNVIYSSNQSYYDLLKAAGMSWKKSQKKNPAKDEKLVKKKEEEIQKKLKDWEEDIKAGKLAVFMIDECHLLWGDVLGFVWGRKDIRVEIPIKNQKSRQSYYGALDYQTHEFILQEYPKADTDNTIQFIQYLREQRPGQKLAIFWDGARYHDSQQFRDFLKELNEGLEEDEWLITCTKFAPNAPEQNPVEDIWLQTKNFLRTFYFLCDSFKRVKELFKIFADGQVFDFPKLYSYGFLPQMT
>NZ_CP051167.1|WP_168571175.1|5626352_5631329_-|hypothetical-protein
MTIDSETGVIVWKPTVIQRSESNSIYLASGVYNVLVRVQDNLGGVDLQSFQVKLTPVNNLPAFTNSSPTFIQPQRGKLFEYRLNALDADGDAEIRYELVNPPTGATLNPDTGILRWTPSQTGEFQFTVKAIDSLGGEASQTITATVVEPRPNTPPEITATPRSSVRIGSTYLYQLPLTDSDGDPLTFNFLQSPAGMELDSQGRIIWTPTPSQFGSHPISLEVNDGEDTTTLSWTLNVSNQTVNRAPSITSTPNLITNLERVYQYQLVGFDPDGDLLLWTLDKAPSGMVIDPNSGMLSWQPNATQIGEHTIAIRVTDATGHFVGQEFDLTVRGINTPPEIVSVPITAAAVGTDYRYQIASTDLENDGGRYSLGIAPDGMQIDPETGLITWTPTAQQSGSVEVEVLVIDGQNGVNRQTYTIEVGSDAINHPPVITSTAKYFAATGVPYRYQIEATDADNDGLIYQPISVPNGMTLDVNTGELRWDSPTFGTHQVVVGVNDGRLGAAQGFTLTVQNDLPPVFNTNEPPTVAIPNRLFSYDIQATDPNGSSLTYRLDDASIALGMSVDELGRLRWIPTVENVGTHAITIEAIDELGTTATQTFNLTVTADNVAPQIQLLPSNVYLVDDDYRADIGSEITFFLQATDNVGITGMQLFINDEPVELSGLGTAKIKIEEFGNIKVRAVAYDAAFNVTESTLEITAIDSSDPDSPVVALAEGLFDETVTASLEIVGTVEDENLDYYTLEVAAGGSSEFREIFRGTESVVDGVLGTFDPSILQNDSYVLRLSAYDKGGNGSTIEERIEVGGEKQGNLNLSFNDLVEIPITGFPIILTRTYDSLNAEDSDDFGYGWRMELVDTDLRTNVPPPSFEQELLDIQNAFTDDTRVYVTLPDGERIDFRFEPTGDRLNSFLSLYGDGAARWYHPTFVADNGSGMTLSVPDTRLILGPDGNYYDLAGVPYNPENSRFGGQYTLTTPEGVVAEIDAKSGDLLKVTDADGYSLTFSDAGIFSSTGEAIALGRDAKGRINTVTDFNNQVIRYQYDEKGDLVAVTDRDNVTTHFDYHQSFDHYLTSVLDPLGRSGANAFYDENGRLQLLLQDGTDLLTNQAPILINDSVLVSANLPATIDLSSLVTDPDGDRVTYHISNALNGTAELLADGTTLSFQPAPDFVGTASFDLVANDGGVRSVNETITVKVSDAPLLSLDVVERDVQLRSDGTTNLVVTANFADRKGVVIPASELTYSTDNPDLVTVESDGTITAKNAEGVAVVRVSYRDEEAVTAIRIGATPTPTNDAEFNVALAEFEGIDPYPDAITLVPGAKRQLQLRLNSLSDSPDLSAAASGTRYYVSDENVVRISEDGKITALSSGYATVTVVHGAAEETIEVRVVEPISGTASIGVNGGAVRSDDGAMVMVPPGALTEETPVSIGQIEESNLSLEIPEKFSFAGSFNLDIGEQPLEFPLQFAIPAPAGVEPGTEVFFLRKGELPALQQGDKWVGSETMHPIWTMVESGIVGDDGMIYTTSPPWRGAYESGEYSIAIPKFDYSVAHLRLAGFSAGVGLGLIAVGGIALAYPKLSPLTYSRPDYFVPGGLIGAGALALASVPVLLDASERSVTTLTIPTVGLPYTTELNVSLNLCLMCQLNPYPILNPFWNGSNFSMTNNKDECCI
>NZ_CP051167.1|WP_168571174.1|5623608_5626452_-|hypothetical-protein
MLDVPTQPVPDTQPVLERLQLQYDEQQGRVLYLEGRNFGTNLDDLEVNFHLGGKVYPGTILAPLSQPEQERIAVTTDFVPLAEAEVSLKRTTHSVIDTQTETETERVKIPIDGCVEMAMVPRQTSDTISLVNTLNPEQVIAQTDSKDLLLADIPVGSPNREDGPRAIAATSNASRAYVTLNKSAQVALVDLTAFKQLDAQPNVEGINGIDLPSHAIPSAIAIDSRDEYAYVADWKTGAIYVIDINPSSDFYNQYIGTIEVENASLGLRQLAMSSDGTRLFATTPGGSDTGRGQILVFNIDPRDRPDNPADPNQNTRKWHQQIGRVEGGYGVEGLAATYDPTKMVFTSRGEEPKGYGVLTILNNDPLSFEAVTHYAQLTLGGLTDYFDVNEAVSVAVMYDEESGTDYAFVAGRNGRMIGSGIESVDGSKAGGNIGIIKDALGPNPTLVAATRPIPNGFTNGVSLSSDNKYLTASYPGIDSTFVFNVKEMLQTVNSTPLEVFEEKPIDDINPSISLAADFKDIGNAIDSFTRKIPYGVPNNSHTGPISLGGGSPFSVATASSRPIVNLQNPIGVFDEETLTPTFKWNFNGEGDETDVCATPVDEDDVKEVRLYVSVFPEGEGLLPRDIWPELDSPTPGRDYNPNRILTATWKEGVWTWNGGSQAGAKDQFTLPDDRMLTAGQEYYWAVEAVINGSPTPVVEDSQFKTPLPPSPSSSPFTSVTVLTRGVEPQNDEEHNRLLNSQINALASKIQEAGGSVMKYNPSTGGWQSVTLNGNSWVATNTTPIEEKPLVLLADWMQGLDASSFYNGGFAEAAADSMFASLVKLDQQYGGKVGEGSGLYDANGNLIRTQGDIFNSPLHFIGLGQGAVVNTEMIQRLGTYFPNAGGTNASNRDLQMTTIDPYDYDPTFPEPVFSTVLDPEVVVWDNVTYADNYSNPKSFVAKIHKNIA
>NZ_CP051167.1|WP_168571816.1|5622611_5623649_+|IS630-family-transposase
MNIIDELDNFIENTTNTKEMKRALAAKMKLSGQPSKKIEEILNVSSSFVSQWKNKAIFEGVESLNLQYKGSKGYLKPEEKTQITSWIRQQEYLRLSDLKRYLQQEYNVIYSSNQSYYDLLKAAGMSWKKSQKKNPAKDEKLVKKKEEEIQKKLKDWEEDIKAGKLAVFMIDECHLLWGDVLGFVWGRKDIRVEIPIKNQKSRQSYYGALDYQTHEFILQEYPKADTDNTIQFIQYLREQRPGQKLAIFWDGARYHDSQQFRDFLKELNEGLEEDEWLITCTKFAPNAPEQNPVEDIWLQTKNFLRTFYFLCDSFKRVKELFKIFADGQVFDFPKLYSYGFLPQMT
>NZ_CP051167.1|WP_168571173.1|5622169_5622556_-|hypothetical-protein
MNHLGLLYYQNKGTDNTLNGKELSTADWNVNLGSWANFDQNLDTGGPHQAAAAWYAGTADLNLSQIPSENGQTIYRRLGDLSSSERPWYTPDHTNANFSHGEEMASLGGDWYGLVPLSFGWGQSITSI
>NZ_CP051167.1|WP_168571172.1|5620476_5622153_-|DNA/RNA-non-specific-endonuclease
MSKDEIQEFSYPNDGWGEYLKTKRVSVEQENNPIPGMRGDFAVPTLFNGNFDAIVYKYSSQNIPSWYIDTPTNPLKQSALIDVAGIPGSTGLPNYALQLGGGNPTQATHDWFMVPDWGNLRFDVFAPVESGELNVKLETIEGQSKNVTIALDRDADFLIDETNSREIPIVKEIYSEIENQIGFGRKGFETFQLKLHLSDSEIAEFRGKPAKISFSLQGGDFVYIDNVFFKSDFLAIANPTEARWNLESSTSVNNLLLEKPQYALSYNADTKLANWVGWKVDKTWVTQPQPEPGEFPTGLLRRPEFIADPDLLASGLSSYDANIFTGLGMDRGHLAPDRDKRRHPKDQLSTYLTTNLIAQSMDNNRFFVSGSDNPRDASAWFNIEDKVVFPRAAQGEELYIFAGAFGNNDNSQPRTNVPELLNLNVNRGNTNPDNLVSQEIHIPKWTWKSIIALEQPGADITSSNIEGFAYITPNRAEPDWNNVSSEGIANPLNVFSQFLNNNRGNITNPTDWRNPDTWRVTIPELTHILNERNRVRDYDFNFDFLSNLPETIQQTLNS
>NZ_CP051167.1|WP_168571171.1|5619817_5620273_+|pentapeptide-repeat-containing-protein
MDGEELLRRYDAGERDFRAIILQHTDLSNVKLDSVNLSGACFYHVNLQSANLKNVNLSSTEWSDCNLSVMQFWLCNLKDATIEQCDLESARFFDCDLRGIRISLSNVSRAAFIRVNFQDAKLGGSGEDPCEFWDVIRPDGVFISGFTYHIT
>NZ_CP051167.1|WP_168571170.1|5615720_5619653_-|RHS-repeat-protein
MPSGVFIVDGDFEVPLGTPITFFTNATDNIGVEGVQLFVDEVPVTLTANGTASYTPSELGTLTAKAVAVDAAGNLGESSIDIRVYDPNDLNPPIVELSPTLGEKPLTDFTDIIGTVTDDNLTNYVLSIAPASGGEFVEIASGNSQITNGKLAEFDPTLLQNDTYILRLTATDESGNSASTEQMVDVAGELKLGNFRLSFTDLEVPVAGIPINLTRTYDTLTTNQSDDFGYGWRLEFRDTDLRTSVGRDELYEQTGIPSVGFEEGTRVYVTLPGGKRTGFTFKPVMDPEIVKALRMGAPLPQSMIFYNPAFETDDGEQVTLSAQKTQLLYNQETGQYYHPSGSPYNPANSFFGGSYTLRTKEGIEYVIDGTTGDLLTVTDTNGNTLTYSDEGIFSSTGKSVTFERNASGRIVAAVDPEGNKIQYEYDENGDLVGVTDREENTTRFEYHEEREHYLEEIIDPLGRTGVRTEYDESGRLKRMLDVNGEAVELVYDPDNSTQTVLDVFGNPTTYVYDERGNIVQKVNAVGGISKQSYDKDNNLLSETDPEGNTIKYDYDSNGNLLAITDPLGNVARYTYNSLGQVLTKTDPLGNTITYTYDSRRNLLSTTNAQGKVIKQTTDEFGNVTSLTDADGNTTQFEYDSFGNVTRQIDVLGNETTYTYDNNGNQLTETVTVTTPEGKKTLVTKWTYDSKGNVLTKTDSSGHVIRHEYDQLGNLTALVEEGTKNRRTEYRYNEKGHLEETLYPDGTLERFVYDKAGRKVAVLDQQGQMTHFVYDALNRLIETIYPDDTPNNLSDNPRTKTEYSQAGQIKAKIDERGYRTEYEDDKTGRRTLMRDALNNETKYTYDSVGNRLSETNARNHTTKFVYDRVGRPIETHYADGSRTVTTYDAVGRKHSFTDQAGRTTYFVYDLLDRLVEVIHPDNTPDDLADNPRTKTEYNELGWVVAEIDERGNRNEYEYDTLGRVIESRSSCGCRRKTITYDEFGNQISETDQMGNTTRFVYDELGRLSETHFPDNTYTTTTYDNLGRVTSITDQVGKKTEFEYDPQGRLVAVVDALKQRTEYGYDFSGNLTSIKNANGDVTTYEYDELGRRVGTVLPEFQYSQTTYDAVGNLLSAKDFNQDSVSYEYDSLNHLTAERFPDGRSLEYTYTPTGLRHTVTEIEAGMTRTTTYKYDERDRLIERTESDGRKIEYTYDGAGNITSVTTSSGTTYYTYDRYNQLETVTTPDLGVTQYAYDKAGNLTRTEFPNGTIELREYDELNRLVFLKNLKVEPSTGQEVTLFSYRYTLNAAGQRTKVEENNGRVIEYTYDDLY
>NZ_CP051167.1|WP_168571179.1|5637547_5638417_-|DUF4114-domain-containing-protein
MQILNNESLFPDSQGDPLISGLVDNPVDPFNNPIKPLESPPTGSELFPINSQYGVEDTSLTDGVSVNNIESSILPSSDNNSPIDPLTGEALPSVQNTDFTSGIFVVGNTGQVNIEFLYDGGAYQSEIGIFSLTGMEEFVPGSAEFIKEAAKRALSHSEQGYIVISDANEAAKFTGDLEEATNFNWGKHEGNKTFLMQPGDKFGIILVPNGTIEEVQENPELTGNKRPLFSLATANPEDAFHVGQIADVTGEGNLFVMEDLRVDVGSDLDYNDLIFSYLELPEPPQSLMN
>NZ_CP051167.1|WP_168571180.1|5639386_5639710_-|hypothetical-protein
MLRSLVRILAGKVKVATPTDQLTSTELTSHELLKLAHALFLKLAAEGLDKAELRGFIKRRYGKPTKFAMTREELEDLLRLLKLYGPAICSRVTGEFDPPTQIQLDFW
>NZ_CP051167.1|WP_168571816.1|5640107_5641145_+|IS630-family-transposase
MNIIDELDNFIENTTNTKEMKRALAAKMKLSGQPSKKIEEILNVSSSFVSQWKNKAIFEGVESLNLQYKGSKGYLKPEEKTQITSWIRQQEYLRLSDLKRYLQQEYNVIYSSNQSYYDLLKAAGMSWKKSQKKNPAKDEKLVKKKEEEIQKKLKDWEEDIKAGKLAVFMIDECHLLWGDVLGFVWGRKDIRVEIPIKNQKSRQSYYGALDYQTHEFILQEYPKADTDNTIQFIQYLREQRPGQKLAIFWDGARYHDSQQFRDFLKELNEGLEEDEWLITCTKFAPNAPEQNPVEDIWLQTKNFLRTFYFLCDSFKRVKELFKIFADGQVFDFPKLYSYGFLPQMT
>NZ_CP051167.1|WP_168571181.1|5642260_5647162_-|hypothetical-protein
MDTTHNAGTLDPNSEQILDQIINTLELSEGEFALIFARCNFRDFRQQSIRRLQEKSPFPILEIPLENPIADLYNPIARAIAETPAKAVMVYGLEELTEIEAILSATNHAREQFRQNFAFPVIIWVNDEISKQFTRVIKDFKSWGISLNFSMSDDRLLQFLKNRGEKGFKIIIEGGELMSPEEIFSPVEQQEINFAVQELERRRVQWSPELNACLNFMAGWRAYLGGELEQALQDYHKSLSFWQGEAIALTRTQALERQAIAHFYIAACHQRQAQWNEAKQAMQACLDTLQIAGREDLKLKYAVELGAVLQQMQGWDELEAFAHQKLSEHRQHPDPLREARYYGFLAEVAYHRQQWTQGGKWAQSALATVAKIEPSPGMPQAYYLLLIALNLQELKEWEGAIAALEQAREIVGIDTEATTATERRPDFDPELYINRILATLHQLYYQQQEYRKAFAIKQIQQRLGYQYGLLAFIGAGQVQPQLRQRDPSGDLAPTFALSGRQDDVDFLIKDRLSQTSHKLAIVYGPSGVGKSSLLHAGLIPQFHLRPLGGRYGLPVMIRKYDRWTEEKRQEWERQQRIRVQAQKQEQARKIEATDRLEEAFAERDRQYRQYLKSRPLSDRHYQNLKARGLSAEAIELGSFGSSERGGMICPAFWGDKIIGFQWRKDPSGFGQIAGGKYIWSKSPLDSKLPNGEMPITALGTAIDGIGNFSEGILKPDIAQSLRSGLWLGAAGGNFPALITQKAIKDFGIKKAIFWPDGGSRVNAHVKASYRNLKALLDKEGIELQFADWGQWNDKSQPDCDELPEGTAIKLKPAAEFFGPLQEANPKRHEFTDEEKQAWKAQQQRQQWEKCYQFTPDRLIQGDWVDLDPDEILGKITAVRAGMGAGKTTALVKLASAFKGKHKILYLGVSNTLLIQTAEKVKGLHFRSEDDEFFFAPDPLGHHLFCIQSLHRFKPQHLEDAIIVLDEATAIIREFVDGSTLTSRPLAEQRFIESNWHDALQHSKAIVALDGYLGDRHCEYLQTVAPHLELTKIAKPVTPKTPIHFHLGSLVEGDVKAGNFSSILKQIIELATQGKRFAIASDSQKTCEALDETLTAMGILEGYRVDSTTVPEDWMKSILKDPNEAILSNKITRFIYSPSAMSGVDISVPDWFDAQFCIFHGVLSADLLSQMVWRIRDCCERHVWVNPKGLGEGGQYTPRAIERTIRFGLAQNLWDSFGEGHGTFDNWQTQLNSPDCRQAYWERAKANYEKANLRECLRWLLEVNGSEVIEAAVEADPEALAQFKNAKDEIKDREAIGAHEADNIDDDEFTRLKKGCNREDRPKVIRHSIRMSLPEIDLDPQWSPEFIRWYLENRDTRSQAKRWFLFQQQETAKSTTSESWIKREGFRAYQFRSYLGEVRALAELGILEVFKTPKSKDDPEVQAIADRWRKDPQIRARLGGRMPAQNPIRSFNWILGLFGIRLRCAQQQRGKNKKKNLYQIDYSLSETANWKAVARAVARTYADKGLQAANDCTIFVGELYNPVENGTEFNTANSAIDTQPTPESETMADPEPMTEVASDAETWKGKWFTIAPDATNPRPDWGQWVGRADGEPFQNPYRRNEWHVIIRVPDMGTVTVPAHSVEIACTEAVAVSTA
>NZ_CP051167.1|WP_168571182.1|5647479_5648820_-|AAA-family-ATPase
MDRNEFKRFFRACNPSKTIWIERPEDKDYYIDFTSVRGTDIVEQLGETISLLSPDPTCQLFTGHIGCGKSTELLRLKFELEKQGFVVVYIDTRDDLEMGDVDVTDVLLAIAQKVLDTLEQQSLNLKPGYFNELLEQCVQFLLTPIELKAEMEFNPEISFLGAKVNLGKIVAKTKDSPQMRDRLRDYLEPKTNTLLQAINGDLIQPANLQLKKQGKEGLVIIIDSLDRVDNRKRSDDKSAVEYLFITRGEQLKELKCHVVYTIPLVLMFSNEREALKKRLGGGNAPMVLPMVPVKLADGQNCEKGLELLRQAILARAFPKLSPKQRRDRITEVVDRPETLDRLCGISGGHVRNLLSLLFRCLQQSKQLPITRDRLEIAIRQERDDLMLAITELEWELLKKVSQTKKVTGEDQYQILLRSLFVFEYRTNEFGRWFDLNPLLEDAPELT
>NZ_CP051167.1|WP_168571183.1|5648991_5649702_-|thiaminase-II
MLDLSKRVGAEPGTLCDRLFQNSRSIWERQFDHPFVEALGNGSLPRENFEFYILQDARFLEQLTKIFAAGAIASDEPAVMEKMCQLALDTIRVERELHETFAREFGLTIAQMEATPLAPTNYAYTRHLLSVVNNGTLPEIITATLPCAWIYAEIGKHFVSLGDPPADHPYRNWIQTYADPSFEEVGTWLRTTLNRITPEDEKTFRRLDEIFTISSRYEWMFWEMAWTLEAWKPQIS
>NZ_CP051167.1|WP_168571184.1|5649719_5650523_-|DUF2993-domain-containing-protein
MEFLTILFSSLLTVISPVNTVSDTVIERELRDRLHGVEVLEVRIDNTPNYQVIRGKIDRFRLAGRGLYVLPDLRIDTLDIETDPIAVDLEKLRRGSRDRAVESLERPAIAAIHLVLTETDLNRALRSPEFLNTLQTVATEIFDSPLLRQNASRYTLVDPQIELLENNRIVFETQLAEKGYSDRLKLTIKTGFRWIDGRQLELSEPQVLVNDRPAPGQFVRGLNAVARRFNLDRAADRGIQARAIRVQIAGDRLETVLCVRSIATHSP
>NZ_CP051167.1|WP_168571185.1|5650644_5652315_-|B12-binding-domain-containing-radical-SAM-protein
MQIPDRNDIVKLYEKLFRKLNAPNTLTSQTQMNTDRILYVRLPCNPIFPIGVVYLADRIHKLFPDVEQQIFDLGTIPPLDFASALDRAIDEFKPSLLVFSWRDIQIYAPVGGRGGNPLQYAFEFYYARNPLVKLRGALGGLRITTAYYTELWRNLGLIKRGLKRAKTYNPDARAVVGGGAVSVFYEQLGKSLPDGTIVSVGEGEALLEKLLRGDSLDDERCYIVGQTEPRDRMIHEKPTDFEKTACNYDYIETIWPAFNYYLQESDFYIGVQTKRGCPHNCCYCIYTVIEGKQVRINPADEVVAEMRQLYDRGIRNFWFTDAQFIPARKFIDDAIELLQKILASGMKDIHWAAYIRADNLTPELCDLMVKTGMNYFEIGITSGSQELVRKMRMGYNLRTVLENCRDLKAAGFNDLVSVNYSFNVIDETFETIRQTIAYHRELERIFGADKVEPAIFFIGLQPHTHLEEYAFDNDILKPGYNPMSLMPWTARKLLWNPEPLGSFFGEVCLEAWRRNPNDFGREVMNILEERLGCGDLEAALSAPIDTAKKSLVGASS
>NZ_CP051167.1|WP_168572026.1|5652712_5653105_+|DUF1830-domain-containing-protein
MAQILDPLPSDRSGRILCCYVNATSKIQIARISNIPNWYFERVVFPGQRLVFEAFSEALLEIHTGMMASAILSDKIPCTRLRIADNDSSGSEDSGDPIEEPTRPQPRRESYDKRPAITDPLAVAALTTIA
>NZ_CP051167.1|WP_168571186.1|5653239_5653674_+|DUF4079-domain-containing-protein
MDLPSFLWLWKIAAWSMGLTIAAYVVLATTGWFVFRARKARRRRVLLKSIHQTVGVAIVGLVLLLLAIGIVGTLGHYGSLGHSVHLVAGLSTVVLVLLSAWSSTQIAPRRPWARTVHVSTNVTLFFVLAWVSWTGWSVVQKYLP

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP051167_7	7.3\|1409863\|19\|NZ_CP051167\|CRISPRCasFinder	1409863-1409881	19	NZ_CP051167.1	1428257-1428275	2	0.895
NZ_CP051167_13	13.1\|2208690\|20\|NZ_CP051167\|PILER-CR	2208690-2208709	20	NZ_CP051167.1	1108681-1108700	2	0.9

1. spacer 7.3|1409863|19|NZ_CP051167|CRISPRCasFinder matches to position: 1428257-1428275, mismatch: 2, identity: 0.895

tgtcggcgtcggcgtaggg	CRISPR spacer
tgtcggcgacggcgaaggg	Protospacer
******** ***** ****

2. spacer 13.1|2208690|20|NZ_CP051167|PILER-CR matches to position: 1108681-1108700, mismatch: 2, identity: 0.9

ttgagcgttttgggcgacgc	CRISPR spacer
ttgggggttttgggcgacgc	Protospacer
***.* **************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP051167_7	7.2\|1409821\|19\|NZ_CP051167\|CRISPRCasFinder	1409821-1409839	19	NZ_AP022578	Mycolicibacterium aubagnense strain JCM 15296 plasmid pJCM15296, complete sequence	86296-86314	0	1.0
NZ_CP051167_7	7.2\|1409821\|19\|NZ_CP051167\|CRISPRCasFinder	1409821-1409839	19	NC_011961	Thermomicrobium roseum DSM 5159 plasmid unnamed, complete sequence	404332-404350	0	1.0
NZ_CP051167_7	7.2\|1409821\|19\|NZ_CP051167\|CRISPRCasFinder	1409821-1409839	19	NC_011961	Thermomicrobium roseum DSM 5159 plasmid unnamed, complete sequence	405809-405827	0	1.0
NZ_CP051167_19	19.7\|4260894\|37\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260894-4260930	37	NZ_CP045289	Curtobacterium flaccumfaciens pv. flaccumfaciens strain P990 plasmid pCff2, complete sequence	13524-13560	5	0.865
NZ_CP051167_6	6.12\|1142876\|34\|NZ_CP051167\|CRT	1142876-1142909	34	NZ_CP015095	Pelagibaca abyssi strain JLT2014 plasmid pPABY4, complete sequence	96247-96280	7	0.794
NZ_CP051167_17	17.2\|4026565\|37\|NZ_CP051167\|CRISPRCasFinder,CRT	4026565-4026601	37	KX879627	Campylobacter phage vB_CjeM_Los1, complete genome	89031-89067	7	0.811
NZ_CP051167_17	17.2\|4026565\|37\|NZ_CP051167\|CRISPRCasFinder,CRT	4026565-4026601	37	NC_042112	Campylobacter phage CP81, complete genome	37451-37487	7	0.811
NZ_CP051167_4	4.32\|1032005\|35\|NZ_CP051167\|CRISPRCasFinder,CRT,PILER-CR	1032005-1032039	35	NZ_CP032341	Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence	738689-738723	8	0.771
NZ_CP051167_4	4.32\|1032005\|35\|NZ_CP051167\|CRISPRCasFinder,CRT,PILER-CR	1032005-1032039	35	NZ_CP012916	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence	309911-309945	8	0.771
NZ_CP051167_17	17.2\|4026565\|37\|NZ_CP051167\|CRISPRCasFinder,CRT	4026565-4026601	37	KF148616	Campylobacter phage CP8, complete genome	91416-91452	8	0.784
NZ_CP051167_17	17.2\|4026565\|37\|NZ_CP051167\|CRISPRCasFinder,CRT	4026565-4026601	37	NC_016562	Campylobacter phage CPX, complete genome	91180-91216	8	0.784
NZ_CP051167_17	17.2\|4026565\|37\|NZ_CP051167\|CRISPRCasFinder,CRT	4026565-4026601	37	JX569801	Campylobacter phage CP30A, complete genome	5087-5123	8	0.784
NZ_CP051167_17	17.14\|4027432\|34\|NZ_CP051167\|CRISPRCasFinder,CRT,PILER-CR	4027432-4027465	34	NZ_CP023000	Rhizobium sp. 11515TR strain 10195 plasmid p11515TR-B, complete sequence	315143-315176	8	0.765
NZ_CP051167_17	17.43\|4026565\|38\|NZ_CP051167\|PILER-CR	4026565-4026602	38	KX879627	Campylobacter phage vB_CjeM_Los1, complete genome	89030-89067	8	0.789
NZ_CP051167_17	17.43\|4026565\|38\|NZ_CP051167\|PILER-CR	4026565-4026602	38	NC_042112	Campylobacter phage CP81, complete genome	37451-37488	8	0.789
NZ_CP051167_19	19.7\|4260894\|37\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260894-4260930	37	MK249136	Blackfly microvirus SF02 isolate 021, complete genome	23-59	8	0.784
NZ_CP051167_5	5.2\|1044327\|35\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	1044327-1044361	35	MH925091	UNVERIFIED: Vibrio phage ValSw4_1, complete genome	30523-30557	9	0.743
NZ_CP051167_5	5.2\|1044327\|35\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	1044327-1044361	35	MN871506	UNVERIFIED: Vibrio phage VspDsh_2, complete genome	30523-30557	9	0.743
NZ_CP051167_5	5.7\|1044690\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	1044690-1044723	34	AP013529	Uncultured Mediterranean phage uvMED DNA, complete genome, group G3, isolate: uvMED-CGR-U-MedDCM-OCT-S40-C13	27080-27113	9	0.735
NZ_CP051167_5	5.13\|1045124\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	1045124-1045157	34	NC_018265	Melissococcus plutonius DAT561 plasmid 1, complete sequence	33308-33341	9	0.735
NZ_CP051167_5	5.13\|1045124\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	1045124-1045157	34	LN681534	Clostridium phage phiCD24-1, complete genome	483-516	9	0.735
NZ_CP051167_5	5.13\|1045124\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	1045124-1045157	34	MN718463	Clostridium phage phiCDKH01, complete genome	19845-19878	9	0.735
NZ_CP051167_11	11.13\|2128425\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	2128425-2128458	34	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	668251-668284	9	0.735
NZ_CP051167_11	11.13\|2128425\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	2128425-2128458	34	NZ_CP012915	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence	1464131-1464164	9	0.735
NZ_CP051167_19	19.7\|4260894\|37\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260894-4260930	37	MN693184	Marine virus AFVG_25M66, complete genome	34038-34074	9	0.757
NZ_CP051167_19	19.8\|4260966\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260966-4260999	34	MN698248	Pelagibacter phage HTVC202P, complete genome	7299-7332	9	0.735
NZ_CP051167_19	19.8\|4260966\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260966-4260999	34	MF351863	Synechococcus phage Bellamy, complete genome	104593-104626	9	0.735
NZ_CP051167_3	3.1\|998534\|32\|NZ_CP051167\|CRISPRCasFinder	998534-998565	32	NZ_AP017962	Synechococcus sp. NIES-970 plasmid plasmid3 DNA, complete sequence	34643-34674	10	0.688
NZ_CP051167_3	3.1\|998534\|32\|NZ_CP051167\|CRISPRCasFinder	998534-998565	32	NZ_CP050268	Salinivibrio costicola strain M318 plasmid pM138.1, complete sequence	28347-28378	10	0.688
NZ_CP051167_3	3.1\|998534\|32\|NZ_CP051167\|CRISPRCasFinder	998534-998565	32	NZ_CP016489	Synechococcus sp. PCC 8807 plasmid unnamed6, complete sequence	6483-6514	10	0.688
NZ_CP051167_5	5.13\|1045124\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	1045124-1045157	34	NZ_CP012100	Bacillus thuringiensis strain HS18-1 plasmid pHS18-1, complete sequence	14205-14238	10	0.706
NZ_CP051167_6	6.12\|1142876\|34\|NZ_CP051167\|CRT	1142876-1142909	34	NZ_CP013054	Sinorhizobium americanum CCGM7 plasmid C, complete sequence	1189296-1189329	10	0.706
NZ_CP051167_6	6.12\|1142876\|34\|NZ_CP051167\|CRT	1142876-1142909	34	NZ_CP029232	Sinorhizobium fredii CCBAU 45436 plasmid pSF45436b, complete sequence	728514-728547	10	0.706
NZ_CP051167_6	6.12\|1142876\|34\|NZ_CP051167\|CRT	1142876-1142909	34	NZ_CP013110	Sinorhizobium americanum strain CFNEI 73 plasmid C, complete sequence	1219658-1219691	10	0.706
NZ_CP051167_6	6.12\|1142876\|34\|NZ_CP051167\|CRT	1142876-1142909	34	NZ_CP029452	Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence	1379773-1379806	10	0.706
NZ_CP051167_6	6.12\|1142876\|34\|NZ_CP051167\|CRT	1142876-1142909	34	NZ_CP023071	Sinorhizobium fredii CCBAU 83666 plasmid pSF83666b, complete sequence	1357751-1357784	10	0.706
NZ_CP051167_11	11.11\|2128281\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	2128281-2128314	34	NZ_CP015881	Ensifer adhaerens strain Casida A plasmid pCasidaAA, complete sequence	1080456-1080489	10	0.706
NZ_CP051167_11	11.12\|2128352\|36\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	2128352-2128387	36	NZ_CP031160	Deinococcus wulumuqiensis strain NEB 479 plasmid pDrdB, complete sequence	47628-47663	10	0.722
NZ_CP051167_19	19.7\|4260894\|37\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260894-4260930	37	NZ_CP039703	Clostridium butyricum strain 29-1 plasmid p-butyl_plas_29-1, complete sequence	511897-511933	10	0.73
NZ_CP051167_19	19.8\|4260966\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260966-4260999	34	NC_022111	Prevotella sp. oral taxon 299 str. F0039 plasmid, complete sequence	507220-507253	10	0.706
NZ_CP051167_4	4.33\|1032077\|36\|NZ_CP051167\|CRISPRCasFinder,CRT,PILER-CR	1032077-1032112	36	NZ_CP009547	Burkholderia sp. 2002721687 plasmid pBTU, complete sequence	154000-154035	11	0.694
NZ_CP051167_4	4.33\|1032077\|36\|NZ_CP051167\|CRISPRCasFinder,CRT,PILER-CR	1032077-1032112	36	NZ_CP013381	Burkholderia sp. Bp5365 strain MSMB43 plasmid pMSMB43, complete sequence	268968-269003	11	0.694
NZ_CP051167_5	5.6\|1044617\|36\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	1044617-1044652	36	CP011076	Brevibacillus laterosporus strain B9 plasmid unnamed2, complete sequence	770733-770768	11	0.694
NZ_CP051167_5	5.13\|1045124\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	1045124-1045157	34	NZ_CP012101	Bacillus thuringiensis strain HS18-1 plasmid pHS18-2, complete sequence	113432-113465	11	0.676
NZ_CP051167_5	5.13\|1045124\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	1045124-1045157	34	NZ_CP040345	Bacillus albus strain DLOU-Yingkou plasmid unnamed1, complete sequence	469364-469397	11	0.676
NZ_CP051167_11	11.19\|2128859\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	2128859-2128892	34	MN045228	Staphylococcus phage Maine, complete genome	15099-15132	11	0.676
NZ_CP051167_16	16.17\|3602354\|38\|NZ_CP051167\|CRISPRCasFinder,PILER-CR,CRT	3602354-3602391	38	NZ_CP016083	Streptomyces sp. SAT1 plasmid unnamed3, complete sequence	549134-549171	11	0.711
NZ_CP051167_19	19.7\|4260894\|37\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260894-4260930	37	MN176220	Bacillus phage 019DV002, complete genome	50382-50418	11	0.703
NZ_CP051167_19	19.7\|4260894\|37\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260894-4260930	37	MN176230	Bacillus phage 056SW001B, complete genome	50750-50786	11	0.703
NZ_CP051167_19	19.7\|4260894\|37\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260894-4260930	37	MN176232	Bacillus phage 280BB001, complete genome	50431-50467	11	0.703
NZ_CP051167_19	19.7\|4260894\|37\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260894-4260930	37	MN176221	Bacillus phage 019DV004, complete genome	50382-50418	11	0.703
NZ_CP051167_19	19.7\|4260894\|37\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260894-4260930	37	MN176231	Bacillus phage 276BB001, complete genome	50430-50466	11	0.703
NZ_CP051167_19	19.7\|4260894\|37\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260894-4260930	37	NZ_CP010581	Bacillus thuringiensis serovar morrisoni strain BGSC 4AA1 plasmid pBMB68, complete sequence	43423-43459	11	0.703
NZ_CP051167_19	19.8\|4260966\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260966-4260999	34	MN694526	Marine virus AFVG_250M936, complete genome	9657-9690	11	0.676
NZ_CP051167_19	19.8\|4260966\|34\|NZ_CP051167\|PILER-CR,CRISPRCasFinder,CRT	4260966-4260999	34	NC_009705	Yersinia pseudotuberculosis IP 31758 plasmid p_153kb, complete sequence	139957-139990	12	0.647

1. spacer 7.2|1409821|19|NZ_CP051167|CRISPRCasFinder matches to NZ_AP022578 (Mycolicibacterium aubagnense strain JCM 15296 plasmid pJCM15296, complete sequence) position: , mismatch: 0, identity: 1.0

ggtcggggtcggcgtcggc	CRISPR spacer
ggtcggggtcggcgtcggc	Protospacer
*******************

2. spacer 7.2|1409821|19|NZ_CP051167|CRISPRCasFinder matches to NC_011961 (Thermomicrobium roseum DSM 5159 plasmid unnamed, complete sequence) position: , mismatch: 0, identity: 1.0

ggtcggggtcggcgtcggc	CRISPR spacer
ggtcggggtcggcgtcggc	Protospacer
*******************

3. spacer 7.2|1409821|19|NZ_CP051167|CRISPRCasFinder matches to NC_011961 (Thermomicrobium roseum DSM 5159 plasmid unnamed, complete sequence) position: , mismatch: 0, identity: 1.0

ggtcggggtcggcgtcggc	CRISPR spacer
ggtcggggtcggcgtcggc	Protospacer
*******************

4. spacer 19.7|4260894|37|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP045289 (Curtobacterium flaccumfaciens pv. flaccumfaciens strain P990 plasmid pCff2, complete sequence) position: , mismatch: 5, identity: 0.865

gtttttctttttgtttttttcttttcttttttccttc	CRISPR spacer
ttctttctttttccttttttcttttcttttttccttt	Protospacer
 *.********* .**********************.

5. spacer 6.12|1142876|34|NZ_CP051167|CRT matches to NZ_CP015095 (Pelagibaca abyssi strain JLT2014 plasmid pPABY4, complete sequence) position: , mismatch: 7, identity: 0.794

-gtctcctgtctcggcatagttgccgaagctcggc	CRISPR spacer
cgccagct-tttcggcataggtgccgtagctcggc	Protospacer
 *.*  ** *.********* ***** ********

6. spacer 17.2|4026565|37|NZ_CP051167|CRISPRCasFinder,CRT matches to KX879627 (Campylobacter phage vB_CjeM_Los1, complete genome) position: , mismatch: 7, identity: 0.811

aatatataaaacataaaaaagaaagggaatatattgg	CRISPR spacer
aatatataatacagaaaaaagaaagggattgatttga	Protospacer
********* *** ************** *.  ***.

7. spacer 17.2|4026565|37|NZ_CP051167|CRISPRCasFinder,CRT matches to NC_042112 (Campylobacter phage CP81, complete genome) position: , mismatch: 7, identity: 0.811

aatatataaaacataaaaaagaaagggaatatattgg	CRISPR spacer
aatatataatacagaaaaaagaaagggattgatttga	Protospacer
********* *** ************** *.  ***.

8. spacer 4.32|1032005|35|NZ_CP051167|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032341 (Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence) position: , mismatch: 8, identity: 0.771

tcggcgaggcgctcgtcggcagcgatcgcccgcca-	CRISPR spacer
ccggggaggcggtcgtcggcagcgatca-gggcgat	Protospacer
.*** ****** ***************.   ** *

9. spacer 4.32|1032005|35|NZ_CP051167|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012916 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence) position: , mismatch: 8, identity: 0.771

tcggcgaggcgctcgtcggcagcgatcgcccgcca-	CRISPR spacer
ccggggaggcggtcgtcggcagcgatca-gggcgat	Protospacer
.*** ****** ***************.   ** *

10. spacer 17.2|4026565|37|NZ_CP051167|CRISPRCasFinder,CRT matches to KF148616 (Campylobacter phage CP8, complete genome) position: , mismatch: 8, identity: 0.784

aatatataaaacataaaaaagaaagggaatatattgg	CRISPR spacer
aatatataatacagaaaaaagaaaggaattgattttg	Protospacer
********* *** ************.* *.  ** *

11. spacer 17.2|4026565|37|NZ_CP051167|CRISPRCasFinder,CRT matches to NC_016562 (Campylobacter phage CPX, complete genome) position: , mismatch: 8, identity: 0.784

aatatataaaacataaaaaagaaagggaatatattgg	CRISPR spacer
aatatataatacagaaaaaagaaaggaattgattttg	Protospacer
********* *** ************.* *.  ** *

12. spacer 17.2|4026565|37|NZ_CP051167|CRISPRCasFinder,CRT matches to JX569801 (Campylobacter phage CP30A, complete genome) position: , mismatch: 8, identity: 0.784

aatatataaaacataaaaaagaaagggaatatattgg	CRISPR spacer
aatatataatacagaaaaaagaaaggaattgatttga	Protospacer
********* *** ************.* *.  ***.

13. spacer 17.14|4027432|34|NZ_CP051167|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP023000 (Rhizobium sp. 11515TR strain 10195 plasmid p11515TR-B, complete sequence) position: , mismatch: 8, identity: 0.765

ggaacgcggtgtccgggacgggaatcgccgcact	CRISPR spacer
gtgccgcgatgtccgggacgggcatcgcccagct	Protospacer
* . ****.************* ******  .**

14. spacer 17.43|4026565|38|NZ_CP051167|PILER-CR matches to KX879627 (Campylobacter phage vB_CjeM_Los1, complete genome) position: , mismatch: 8, identity: 0.789

aatatataaaacataaaaaagaaagggaatatattggc	CRISPR spacer
aatatataatacagaaaaaagaaagggattgatttgaa	Protospacer
********* *** ************** *.  ***.

15. spacer 17.43|4026565|38|NZ_CP051167|PILER-CR matches to NC_042112 (Campylobacter phage CP81, complete genome) position: , mismatch: 8, identity: 0.789

aatatataaaacataaaaaagaaagggaatatattggc	CRISPR spacer
aatatataatacagaaaaaagaaagggattgatttgaa	Protospacer
********* *** ************** *.  ***.

16. spacer 19.7|4260894|37|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to MK249136 (Blackfly microvirus SF02 isolate 021, complete genome) position: , mismatch: 8, identity: 0.784

gtttttctttttgtttttttcttttcttttttccttc	CRISPR spacer
ttttttcgttttgtttttttctttttttgtatttttt	Protospacer
 ****** *****************.** * *..**.

17. spacer 5.2|1044327|35|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to MH925091 (UNVERIFIED: Vibrio phage ValSw4_1, complete genome) position: , mismatch: 9, identity: 0.743

attaaataaaactcctattgaaaat-----ttattaggaa	CRISPR spacer
attaaataaaactcctattagaaataaacgttttc-----	Protospacer
*******************..****     ** *.

18. spacer 5.2|1044327|35|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to MN871506 (UNVERIFIED: Vibrio phage VspDsh_2, complete genome) position: , mismatch: 9, identity: 0.743

attaaataaaactcctattgaaaat-----ttattaggaa	CRISPR spacer
attaaataaaactcctattagaaataaacgttttc-----	Protospacer
*******************..****     ** *.

19. spacer 5.7|1044690|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to AP013529 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G3, isolate: uvMED-CGR-U-MedDCM-OCT-S40-C13) position: , mismatch: 9, identity: 0.735

agtaaggcgtcgaagaacccatcatactcttcat	CRISPR spacer
agtaaggcctcaaagaacccatcatcgccaggct	Protospacer
******** **.*************  .*    *

20. spacer 5.13|1045124|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to NC_018265 (Melissococcus plutonius DAT561 plasmid 1, complete sequence) position: , mismatch: 9, identity: 0.735

ttttgtatgcttttttgtatacttttttgtcgag	CRISPR spacer
tttcaattgcttttttatatacttttttatctca	Protospacer
***..  *********.***********.**  .

21. spacer 5.13|1045124|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to LN681534 (Clostridium phage phiCD24-1, complete genome) position: , mismatch: 9, identity: 0.735

ttttgtatgcttttttgtatacttttttgtcgag	CRISPR spacer
ttttgtatgctttcttgtatgcttctgttgcatt	Protospacer
*************.******.***.* *  *.

22. spacer 5.13|1045124|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to MN718463 (Clostridium phage phiCDKH01, complete genome) position: , mismatch: 9, identity: 0.735

ttttgtatgcttttttgtatacttttttgtcgag	CRISPR spacer
ttttgtatgctttcttgtatgcttctgttgcatt	Protospacer
*************.******.***.* *  *.

23. spacer 11.13|2128425|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.735

cagactaactgtcaaaattgccgccgctcgattt	CRISPR spacer
ttggcaaactgtcaaaaatgccgccgttcgttgg	Protospacer
. *.* *********** ********.*** *

24. spacer 11.13|2128425|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP012915 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence) position: , mismatch: 9, identity: 0.735

cagactaactgtcaaaattgccgccgctcgattt	CRISPR spacer
ttggcaaactgtcaaaaatgccgccgttcgttgg	Protospacer
. *.* *********** ********.*** *

25. spacer 19.7|4260894|37|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to MN693184 (Marine virus AFVG_25M66, complete genome) position: , mismatch: 9, identity: 0.757

gtttttctttttgtttttttcttttcttttttccttc	CRISPR spacer
ctttttcttttggttcttttcttttcttttgattgcc	Protospacer
 ********** ***.**************  .. .*

26. spacer 19.8|4260966|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to MN698248 (Pelagibacter phage HTVC202P, complete genome) position: , mismatch: 9, identity: 0.735

ttgtttcttcttcttctttttatccccacccctg	CRISPR spacer
ttatttcttcttcttttttttatcctgaaacagt	Protospacer
**.************.*********. *  *

27. spacer 19.8|4260966|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to MF351863 (Synechococcus phage Bellamy, complete genome) position: , mismatch: 9, identity: 0.735

ttgtttcttcttcttctttttatccccacccctg	CRISPR spacer
ttttttctttttcttctttttatcttcggcaacg	Protospacer
** ******.**************..*. *  .*

28. spacer 3.1|998534|32|NZ_CP051167|CRISPRCasFinder matches to NZ_AP017962 (Synechococcus sp. NIES-970 plasmid plasmid3 DNA, complete sequence) position: , mismatch: 10, identity: 0.688

tttttttgaggggcgatcgccttttttccctc	CRISPR spacer
tacttctgaagggcgatcgcctttttaaggct	Protospacer
* .**.***.****************    ..

29. spacer 3.1|998534|32|NZ_CP051167|CRISPRCasFinder matches to NZ_CP050268 (Salinivibrio costicola strain M318 plasmid pM138.1, complete sequence) position: , mismatch: 10, identity: 0.688

tttttttgaggggcgatcgccttttttccctc	CRISPR spacer
ggttttagaggggcgaccgccttttacaaaac	Protospacer
  **** *********.******** .    *

30. spacer 3.1|998534|32|NZ_CP051167|CRISPRCasFinder matches to NZ_CP016489 (Synechococcus sp. PCC 8807 plasmid unnamed6, complete sequence) position: , mismatch: 10, identity: 0.688

tttttttgaggggcgatcgccttttttccctc	CRISPR spacer
ttttttagagcggcgatcgccttcaaagtagc	Protospacer
****** *** ************.    .  *

31. spacer 5.13|1045124|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP012100 (Bacillus thuringiensis strain HS18-1 plasmid pHS18-1, complete sequence) position: , mismatch: 10, identity: 0.706

ttttgtatgcttttttgtatacttttttgtcgag	CRISPR spacer
taaagtatgtatttttgtatacttttttacaatg	Protospacer
*   *****. *****************.. . *

32. spacer 6.12|1142876|34|NZ_CP051167|CRT matches to NZ_CP013054 (Sinorhizobium americanum CCGM7 plasmid C, complete sequence) position: , mismatch: 10, identity: 0.706

gtctcctgtctcggcatagttgccgaagctcggc	CRISPR spacer
gcccagcagttcggcatagttgccgaggcccggc	Protospacer
*.*.  .. .****************.**.****

33. spacer 6.12|1142876|34|NZ_CP051167|CRT matches to NZ_CP029232 (Sinorhizobium fredii CCBAU 45436 plasmid pSF45436b, complete sequence) position: , mismatch: 10, identity: 0.706

gtctcctgtctcggcatagttgccgaagctcggc	CRISPR spacer
gcccagcagttcggcatagtttccgaagcccggc	Protospacer
*.*.  .. .*********** *******.****

34. spacer 6.12|1142876|34|NZ_CP051167|CRT matches to NZ_CP013110 (Sinorhizobium americanum strain CFNEI 73 plasmid C, complete sequence) position: , mismatch: 10, identity: 0.706

gtctcctgtctcggcatagttgccgaagctcggc	CRISPR spacer
gcccagcagttcggcatagttgccgaggcccggc	Protospacer
*.*.  .. .****************.**.****

35. spacer 6.12|1142876|34|NZ_CP051167|CRT matches to NZ_CP029452 (Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence) position: , mismatch: 10, identity: 0.706

gtctcctgtctcggcatagttgccgaagctcggc	CRISPR spacer
gcccagcagttcggcatagtttccgaagcccggc	Protospacer
*.*.  .. .*********** *******.****

36. spacer 6.12|1142876|34|NZ_CP051167|CRT matches to NZ_CP023071 (Sinorhizobium fredii CCBAU 83666 plasmid pSF83666b, complete sequence) position: , mismatch: 10, identity: 0.706

gtctcctgtctcggcatagttgccgaagctcggc	CRISPR spacer
gcccagcagttcggcatagtttccgaagcccggc	Protospacer
*.*.  .. .*********** *******.****

37. spacer 11.11|2128281|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP015881 (Ensifer adhaerens strain Casida A plasmid pCasidaAA, complete sequence) position: , mismatch: 10, identity: 0.706

cccgatcgatttccgacatctccttgatcgttcg	CRISPR spacer
ggtggccgatttccgaaatctcctcgatcggcag	Protospacer
  .*..********** *******.***** . *

38. spacer 11.12|2128352|36|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP031160 (Deinococcus wulumuqiensis strain NEB 479 plasmid pDrdB, complete sequence) position: , mismatch: 10, identity: 0.722

caatttggcctgagcatgcgcagcagctcgaagctg	CRISPR spacer
tcggtgcgcccgagcatgcgcagcagctcgtaggcg	Protospacer
. . *  ***.******************* ** .*

39. spacer 19.7|4260894|37|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP039703 (Clostridium butyricum strain 29-1 plasmid p-butyl_plas_29-1, complete sequence) position: , mismatch: 10, identity: 0.73

gtttttctttttgtttttttcttttcttttttccttc	CRISPR spacer
tctagtctttttcttttttccttttctttttttagtt	Protospacer
 .*  ******* ******.************.  *.

40. spacer 19.8|4260966|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to NC_022111 (Prevotella sp. oral taxon 299 str. F0039 plasmid, complete sequence) position: , mismatch: 10, identity: 0.706

ttgtttcttcttcttctttttatccccacccctg	CRISPR spacer
ttgtttcttcttcatctttatatcaaatttaatg	Protospacer
************* ***** ****    ..  **

41. spacer 4.33|1032077|36|NZ_CP051167|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP009547 (Burkholderia sp. 2002721687 plasmid pBTU, complete sequence) position: , mismatch: 11, identity: 0.694

tcgcgttccgacgagggcgcgatcggcgatccttgt	CRISPR spacer
caagacagcaacgcgggcgcgatcggcgatcctggt	Protospacer
. . ..  *.*** ******************* **

42. spacer 4.33|1032077|36|NZ_CP051167|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013381 (Burkholderia sp. Bp5365 strain MSMB43 plasmid pMSMB43, complete sequence) position: , mismatch: 11, identity: 0.694

tcgcgttccgacgagggcgcgatcggcgatccttgt	CRISPR spacer
caagacagcaacgcgggcgcgatcggcgatcctggt	Protospacer
. . ..  *.*** ******************* **

43. spacer 5.6|1044617|36|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to CP011076 (Brevibacillus laterosporus strain B9 plasmid unnamed2, complete sequence) position: , mismatch: 11, identity: 0.694

cgtgacactttcgatgaattcaattaattcttgttt	CRISPR spacer
tagattcatttcgatgaattcaattgaatcttgtat	Protospacer
.. . .  *****************.* ****** *

44. spacer 5.13|1045124|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP012101 (Bacillus thuringiensis strain HS18-1 plasmid pHS18-2, complete sequence) position: , mismatch: 11, identity: 0.676

ttttgtatgcttttttgtatacttttttgtcgag	CRISPR spacer
ttttgtatgtttttttgtatatttaaggtataaa	Protospacer
*********.***********.**      ..*.

45. spacer 5.13|1045124|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP040345 (Bacillus albus strain DLOU-Yingkou plasmid unnamed1, complete sequence) position: , mismatch: 11, identity: 0.676

ttttgtatgcttttttgtatacttttttgtcgag	CRISPR spacer
aaaactatgctttttagtatagttttttgccaga	Protospacer
     ********** ***** *******.*...

46. spacer 11.19|2128859|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to MN045228 (Staphylococcus phage Maine, complete genome) position: , mismatch: 11, identity: 0.676

ttatcggtaaatagtagagtatgggctaataata	CRISPR spacer
agagaaagtaatattagagtatgggataataatg	Protospacer
  *  ..  **** *********** *******.

47. spacer 16.17|3602354|38|NZ_CP051167|CRISPRCasFinder,PILER-CR,CRT matches to NZ_CP016083 (Streptomyces sp. SAT1 plasmid unnamed3, complete sequence) position: , mismatch: 11, identity: 0.711

gaggtcagcgccccggaggtcagcgccccggagatcgg	CRISPR spacer
ctcatcagctccccggcggtcagcgccccggccttggc	Protospacer
   .***** ****** **************   * *

48. spacer 19.7|4260894|37|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to MN176220 (Bacillus phage 019DV002, complete genome) position: , mismatch: 11, identity: 0.703

gtttttctttttgtttttttcttttcttttttccttc	CRISPR spacer
aaacctcttttagtctttttcttttcttttttttatt	Protospacer
.  ..****** **.*****************.. *.

49. spacer 19.7|4260894|37|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to MN176230 (Bacillus phage 056SW001B, complete genome) position: , mismatch: 11, identity: 0.703

gtttttctttttgtttttttcttttcttttttccttc	CRISPR spacer
aaacctcttttagtctttttcttttcttttttttatt	Protospacer
.  ..****** **.*****************.. *.

50. spacer 19.7|4260894|37|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to MN176232 (Bacillus phage 280BB001, complete genome) position: , mismatch: 11, identity: 0.703

gtttttctttttgtttttttcttttcttttttccttc	CRISPR spacer
aaacctcttttagtctttttcttttcttttttttatt	Protospacer
.  ..****** **.*****************.. *.

51. spacer 19.7|4260894|37|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to MN176221 (Bacillus phage 019DV004, complete genome) position: , mismatch: 11, identity: 0.703

gtttttctttttgtttttttcttttcttttttccttc	CRISPR spacer
aaacctcttttagtctttttcttttcttttttttatt	Protospacer
.  ..****** **.*****************.. *.

52. spacer 19.7|4260894|37|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to MN176231 (Bacillus phage 276BB001, complete genome) position: , mismatch: 11, identity: 0.703

gtttttctttttgtttttttcttttcttttttccttc	CRISPR spacer
aaacctcttttagtctttttcttttcttttttttatt	Protospacer
.  ..****** **.*****************.. *.

53. spacer 19.7|4260894|37|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP010581 (Bacillus thuringiensis serovar morrisoni strain BGSC 4AA1 plasmid pBMB68, complete sequence) position: , mismatch: 11, identity: 0.703

gtttttctttttgtttttttcttttcttttttccttc	CRISPR spacer
tgcaatttttttatttttttctttacttttttctata	Protospacer
  .  *.*****.*********** ********. *

54. spacer 19.8|4260966|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to MN694526 (Marine virus AFVG_250M936, complete genome) position: , mismatch: 11, identity: 0.676

ttgtttcttcttcttctttttatccccacccctg	CRISPR spacer
tatcttcttcttctcctttatatccccagtatac	Protospacer
*  .**********.**** ******** . .

55. spacer 19.8|4260966|34|NZ_CP051167|PILER-CR,CRISPRCasFinder,CRT matches to NC_009705 (Yersinia pseudotuberculosis IP 31758 plasmid p_153kb, complete sequence) position: , mismatch: 12, identity: 0.647

ttgtttcttcttcttctttttatccccacccctg---	CRISPR spacer
---ttgcttcttcttcttctttttctctttcttgaat	Protospacer
   ** ************.** *.*.* ..*.**

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

1052034 : 1061870

Catovirus(33.33%)

transposase

The bacterium proteins that are colored denote the protein is present at specific phage-related keywords (such as 'capsid', 'head', 'integrase', 'plate', 'tail', 'fiber', 'coat', 'transposase', 'portal', 'terminase', 'protease' or 'lysin' and 'tRNA')

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_168568030.1\|1052034_1054035_-	serine/threonine protein kinase	A0A1V0SBL0	Catovirus	1.9e-08	21.4
WP_168568031.1\|1054074_1054533_-	GatB/YqeY domain-containing protein	A0A292GL36	Xanthomonas_phage	3.9e-18	45.3
WP_168568032.1\|1055028_1056045_+	ribose-phosphate pyrophosphokinase	A0A1V0SHF7	Hokovirus	4.9e-45	33.6
WP_168568033.1\|1056274_1056847_+\|transposase	IS607 family transposase	Q331V0	Clostridium_botulinum_C_phage	1.2e-43	46.6
WP_168568034.1\|1056860_1057934_+\|transposase	transposase	A0A1V0S9X0	Catovirus	4.1e-26	33.3
WP_168568035.1\|1058004_1058469_-	hypothetical protein	NA	NA	NA	NA
WP_168568036.1\|1059169_1060132_+	protochlorophyllide reductase	NA	NA	NA	NA
WP_168568037.1\|1060205_1061870_-	ABC transporter ATP-binding protein	G9BWD6	Planktothrix_phage	1.9e-22	34.4

DBSCAN-SWA_2

1744912 : 1796531

Thermus_phage(20.0%)

tail,protease,tRNA,transposase

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_168568520.1\|1744912_1745869_+\|tRNA	tRNA epoxyqueuosine(34) reductase QueG	NA	NA	NA	NA
WP_168568521.1\|1745917_1746739_-	hypothetical protein	NA	NA	NA	NA
WP_168568522.1\|1747023_1747599_-	TPM domain-containing protein	NA	NA	NA	NA
WP_168568523.1\|1748235_1751868_-	methionine synthase	NA	NA	NA	NA
WP_168571783.1\|1752949_1755388_+	PAS domain-containing protein	NA	NA	NA	NA
WP_168571784.1\|1755524_1756847_+	CHAT domain-containing protein	NA	NA	NA	NA
WP_168568524.1\|1757697_1758975_+\|transposase	transposase	A0A068A1P5	Thermus_phage	2.9e-42	30.2
WP_168568525.1\|1759091_1761581_+	diguanylate cyclase	NA	NA	NA	NA
WP_168568526.1\|1761645_1762563_-	hypothetical protein	NA	NA	NA	NA
WP_168568527.1\|1762817_1764356_-	mercuric reductase	NA	NA	NA	NA
WP_168571785.1\|1764399_1764942_-	TVP38/TMEM64 family protein	NA	NA	NA	NA
WP_168571786.1\|1765300_1767316_-	glycogen debranching protein	NA	NA	NA	NA
WP_168568528.1\|1767579_1767813_-	hypothetical protein	NA	NA	NA	NA
WP_168568529.1\|1768267_1768879_+	cupin	NA	NA	NA	NA
WP_168568530.1\|1768880_1769336_-	DUF4281 domain-containing protein	NA	NA	NA	NA
WP_168568531.1\|1770162_1770762_+	SH3 domain-containing protein	NA	NA	NA	NA
WP_168568532.1\|1771549_1773754_-	EAL domain-containing protein	G3MA91	Bacillus_virus	3.2e-17	33.3
WP_168568533.1\|1777441_1778650_+	hypothetical protein	NA	NA	NA	NA
WP_168568534.1\|1778753_1779242_+\|protease	ATP-dependent zinc protease	NA	NA	NA	NA
WP_168568535.1\|1779238_1780144_+	30S ribosomal protein S6--L-glutamate ligase	A0A1D7SR78	Cyanophage	2.0e-34	32.5
WP_168568536.1\|1780219_1781200_+	succinylglutamate desuccinylase/aspartoacylase family protein	NA	NA	NA	NA
WP_168568537.1\|1781405_1781582_+	hypothetical protein	NA	NA	NA	NA
WP_168568538.1\|1781555_1781918_-	hypothetical protein	NA	NA	NA	NA
WP_168568539.1\|1782091_1782394_+	hypothetical protein	NA	NA	NA	NA
WP_168568540.1\|1782503_1782653_-	hypothetical protein	NA	NA	NA	NA
WP_168568541.1\|1782789_1783233_+	hypothetical protein	NA	NA	NA	NA
WP_168568542.1\|1783244_1783391_-	hypothetical protein	NA	NA	NA	NA
WP_168568543.1\|1784302_1784878_-	hypothetical protein	NA	NA	NA	NA
WP_168568544.1\|1785019_1786372_-	3-phosphoshikimate 1-carboxyvinyltransferase	NA	NA	NA	NA
WP_168568545.1\|1786618_1787110_+	hypothetical protein	NA	NA	NA	NA
WP_168568546.1\|1787116_1788835_-	hypothetical protein	NA	NA	NA	NA
WP_168568547.1\|1788988_1789468_-	hypothetical protein	NA	NA	NA	NA
WP_168568548.1\|1789615_1790335_-	M23 family metallopeptidase	A0A075BS18	Microcystis_phage	1.9e-27	50.4
WP_168568549.1\|1790752_1791538_+	DUF2927 domain-containing protein	NA	NA	NA	NA
WP_168568550.1\|1791560_1792409_-	hypothetical protein	NA	NA	NA	NA
WP_168568551.1\|1792493_1792847_-	hypothetical protein	NA	NA	NA	NA
WP_168568552.1\|1792853_1793342_-\|tail	phage tail protein	NA	NA	NA	NA
WP_168568553.1\|1793406_1793544_-	hypothetical protein	NA	NA	NA	NA
WP_168568554.1\|1793613_1794093_-\|tail	phage tail protein	NA	NA	NA	NA
WP_168568555.1\|1794190_1794664_-\|tail	phage tail protein	NA	NA	NA	NA
WP_168568556.1\|1794821_1796531_-\|tail	phage tail sheath family protein	A0A127AW39	Bacillus_phage	3.9e-18	27.9

DBSCAN-SWA_3

4424511 : 4490354

Hokovirus(33.33%)

protease,tRNA,transposase

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_168570358.1\|4424511_4425708_-\|transposase	ISAs1 family transposase	NA	NA	NA	NA
WP_168570359.1\|4426120_4426690_-	pentapeptide repeat-containing protein	NA	NA	NA	NA
WP_168570360.1\|4426815_4428630_-\|tRNA	proline--tRNA ligase	NA	NA	NA	NA
WP_168570361.1\|4428839_4432340_-	PAS domain S-box protein	A0A1V0SGX0	Hokovirus	8.7e-33	38.9
WP_168570362.1\|4432908_4433124_+	hypothetical protein	NA	NA	NA	NA
WP_168570363.1\|4433156_4433756_+	NfeD-like protein	NA	NA	NA	NA
WP_168570364.1\|4433803_4435165_+	flotillin family protein	NA	NA	NA	NA
WP_168570365.1\|4435179_4436739_+	flotillin family protein	NA	NA	NA	NA
WP_168570366.1\|4438161_4438818_+	sugar transferase	NA	NA	NA	NA
WP_168570367.1\|4439343_4439553_-	DUF433 domain-containing protein	NA	NA	NA	NA
WP_168570368.1\|4440200_4441022_-\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_168570369.1\|4441039_4441327_-\|protease	ATP-dependent Clp protease adapter ClpS	NA	NA	NA	NA
WP_168570370.1\|4441505_4444670_-	hypothetical protein	NA	NA	NA	NA
WP_168570371.1\|4445179_4446217_+	class II fructose-bisphosphatase	NA	NA	NA	NA
WP_168570372.1\|4446630_4447935_+\|tRNA	glutamyl-tRNA reductase	NA	NA	NA	NA
WP_168570373.1\|4448074_4451065_+	COG1615 family transporter	NA	NA	NA	NA
WP_168570374.1\|4451110_4451335_+	hypothetical protein	NA	NA	NA	NA
WP_168570375.1\|4451377_4451644_+	cytotoxic translational repressor of toxin-antitoxin stability system	NA	NA	NA	NA
WP_168570376.1\|4451686_4452409_+	pyridoxine 5'-phosphate synthase	NA	NA	NA	NA
WP_168570377.1\|4452598_4452931_+	DUF2488 family protein	NA	NA	NA	NA
WP_168570378.1\|4453121_4453814_+	hypothetical protein	NA	NA	NA	NA
WP_168570379.1\|4453920_4454376_-	divergent PAP2 family protein	NA	NA	NA	NA
WP_168570380.1\|4454389_4455316_-	polyprenyl synthetase family protein	NA	NA	NA	NA
WP_168570381.1\|4455632_4456517_-	bifunctional methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase FolD	A0A249XZQ2	Enterococcus_phage	8.3e-33	37.4
WP_168570382.1\|4456709_4458974_+	CHAT domain-containing protein	NA	NA	NA	NA
WP_168570383.1\|4458981_4460613_-	hypothetical protein	NA	NA	NA	NA
WP_168570384.1\|4460873_4461230_+	iron-sulfur cluster assembly accessory protein	A0A1B1IT29	uncultured_Mediterranean_phage	3.5e-14	43.0
WP_168570385.1\|4461421_4461841_+	hypothetical protein	NA	NA	NA	NA
WP_168570386.1\|4462105_4464052_+	alpha/beta hydrolase	NA	NA	NA	NA
WP_168570387.1\|4464371_4464710_-\|transposase	transposase	A0A1V0SDE2	Indivirus	8.7e-15	40.6
WP_168570195.1\|4465017_4465602_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_168571951.1\|4465612_4466218_+\|transposase	transposase	NA	NA	NA	NA
WP_168570388.1\|4466520_4466661_-	hypothetical protein	NA	NA	NA	NA
WP_168570389.1\|4466843_4467002_-	hypothetical protein	NA	NA	NA	NA
WP_168570390.1\|4468444_4469641_-	N-acetyltransferase	NA	NA	NA	NA
WP_168570391.1\|4469726_4470431_-	RibD family protein	NA	NA	NA	NA
WP_168570392.1\|4470587_4470803_+	RNA-binding S4 domain-containing protein	NA	NA	NA	NA
WP_168570393.1\|4470847_4473931_-	response regulator	A0A1V0SGX0	Hokovirus	2.3e-45	32.8
WP_168570394.1\|4474633_4474804_-	hypothetical protein	NA	NA	NA	NA
WP_168570395.1\|4475392_4478308_+	calcium-translocating P-type ATPase, PMCA-type	M1HK51	Paramecium_bursaria_Chlorella_virus	3.5e-96	30.6
WP_168570396.1\|4479681_4481262_-\|tRNA	lysine--tRNA ligase	NA	NA	NA	NA
WP_168570397.1\|4481412_4482240_-	nucleoside triphosphate pyrophosphohydrolase	NA	NA	NA	NA
WP_168570398.1\|4482428_4483031_-	metal-binding protein	NA	NA	NA	NA
WP_168570399.1\|4483439_4483724_-	hypothetical protein	NA	NA	NA	NA
WP_168570400.1\|4483956_4484193_-	hypothetical protein	NA	NA	NA	NA
WP_168570401.1\|4484248_4484419_-	ssl1498 family light-harvesting-like protein	NA	NA	NA	NA
WP_168570402.1\|4484656_4485478_-	DnaJ domain-containing protein	NA	NA	NA	NA
WP_168571952.1\|4485539_4486307_-	tryptophan-rich sensory protein	NA	NA	NA	NA
WP_168570403.1\|4486516_4487986_+	hypothetical protein	NA	NA	NA	NA
WP_168570404.1\|4488250_4488754_+	hypothetical protein	NA	NA	NA	NA
WP_168571816.1\|4489316_4490354_-\|transposase	IS630 family transposase	NA	NA	NA	NA

DBSCAN-SWA_4

5509990 : 5517743

Paramecium_bursaria_Chlorella_virus(33.33%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_168572017.1\|5509990_5510773_+	metal ABC transporter ATP-binding protein	A0A285PWH2	Cedratvirus	9.7e-09	27.6
WP_168571091.1\|5510850_5511258_-	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_168571092.1\|5511401_5512307_+	metal ABC transporter permease	NA	NA	NA	NA
WP_168571093.1\|5512284_5513145_-	N-carbamoylputrescine amidase	M1H5W0	Paramecium_bursaria_Chlorella_virus	8.0e-73	47.6
WP_168571094.1\|5513247_5514312_-	agmatine deiminase family protein	A7RCL2	Paramecium_bursaria_Chlorella_virus	3.2e-55	34.1
WP_168571095.1\|5515038_5515248_-	hypothetical protein	NA	NA	NA	NA
WP_168571096.1\|5515878_5516598_+	FAD-dependent thymidylate synthase	G8EY29	Synechococcus_phage	5.9e-69	53.6
WP_168571097.1\|5516647_5517073_-	dUTP diphosphatase	A0A1L2BX65	Bacteriophage	1.7e-36	52.9
WP_168572018.1\|5517245_5517743_+	dCMP deaminase family protein	A0A160DDE4	Gordonia_phage	2.7e-20	40.4

DBSCAN-SWA_5

5603456 : 5686394

Bacillus_phage(14.29%)

protease,transposase

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_168571163.1\|5603456_5606483_-\|transposase	Tn3 family transposase	A0A125RQ78	Bacillus_phage	9.8e-283	50.0
WP_168571164.1\|5606585_5607233_+	recombinase family protein	A0JC18	Ralstonia_phage	1.0e-11	35.3
WP_168571165.1\|5607610_5608330_+	recombinase family protein	A6M972	Geobacillus_virus	2.0e-24	33.9
WP_168572024.1\|5608500_5608902_+	HNH endonuclease	NA	NA	NA	NA
WP_168571166.1\|5609360_5609543_+	hypothetical protein	NA	NA	NA	NA
WP_168571167.1\|5609661_5610060_-	hypothetical protein	NA	NA	NA	NA
WP_168572025.1\|5610073_5612935_-	RHS repeat protein	NA	NA	NA	NA
WP_168571168.1\|5612988_5614128_-	hypothetical protein	NA	NA	NA	NA
WP_168571169.1\|5614142_5615693_-	hypothetical protein	NA	NA	NA	NA
WP_168571170.1\|5615720_5619653_-	RHS repeat protein	NA	NA	NA	NA
WP_168571171.1\|5619817_5620273_+	pentapeptide repeat-containing protein	NA	NA	NA	NA
WP_168571172.1\|5620476_5622153_-	DNA/RNA non-specific endonuclease	NA	NA	NA	NA
WP_168571173.1\|5622169_5622556_-	hypothetical protein	NA	NA	NA	NA
WP_168571816.1\|5622611_5623649_+\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_168571174.1\|5623608_5626452_-	hypothetical protein	NA	NA	NA	NA
WP_168571175.1\|5626352_5631329_-	hypothetical protein	NA	NA	NA	NA
WP_168571816.1\|5631863_5632901_+\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_168571176.1\|5632865_5636444_-	DUF4114 domain-containing protein	NA	NA	NA	NA
WP_168571177.1\|5636688_5636925_+	hypothetical protein	NA	NA	NA	NA
WP_168571178.1\|5636931_5637468_+	hypothetical protein	NA	NA	NA	NA
WP_168571179.1\|5637547_5638417_-	DUF4114 domain-containing protein	NA	NA	NA	NA
WP_168571180.1\|5639386_5639710_-	hypothetical protein	NA	NA	NA	NA
WP_168571816.1\|5640107_5641145_+\|transposase	IS630 family transposase	NA	NA	NA	NA
WP_168571181.1\|5642260_5647162_-	hypothetical protein	A0A2D2W6Z8	Pectobacterium_phage	1.1e-06	24.2
WP_168571182.1\|5647479_5648820_-	AAA family ATPase	NA	NA	NA	NA
WP_168571183.1\|5648991_5649702_-	thiaminase II	NA	NA	NA	NA
WP_168571184.1\|5649719_5650523_-	DUF2993 domain-containing protein	NA	NA	NA	NA
WP_168571185.1\|5650644_5652315_-	B12-binding domain-containing radical SAM protein	NA	NA	NA	NA
WP_168572026.1\|5652712_5653105_+	DUF1830 domain-containing protein	NA	NA	NA	NA
WP_168571186.1\|5653239_5653674_+	DUF4079 domain-containing protein	NA	NA	NA	NA
WP_168571187.1\|5653737_5654313_+	hypothetical protein	NA	NA	NA	NA
WP_168571188.1\|5654345_5655116_+	ATP-binding cassette domain-containing protein	G9BWD6	Planktothrix_phage	1.7e-18	34.0
WP_168571189.1\|5655142_5655943_-	response regulator transcription factor	NA	NA	NA	NA
WP_168571190.1\|5655926_5656139_-	hypothetical protein	NA	NA	NA	NA
WP_168571191.1\|5656795_5657047_+	hypothetical protein	NA	NA	NA	NA
WP_168571192.1\|5657286_5657610_-	Grx4 family monothiol glutaredoxin	NA	NA	NA	NA
WP_168571193.1\|5657700_5657961_-	BolA/IbaG family iron-sulfur metabolism protein	NA	NA	NA	NA
WP_168571194.1\|5658403_5658607_-	hypothetical protein	NA	NA	NA	NA
WP_168572027.1\|5658647_5659265_-	hypothetical protein	NA	NA	NA	NA
WP_168571195.1\|5659604_5661770_+	S8 family serine peptidase	NA	NA	NA	NA
WP_168571196.1\|5661795_5662521_-	1-acyl-sn-glycerol-3-phosphate acyltransferase	NA	NA	NA	NA
WP_168571197.1\|5662614_5663136_-	nucleoside deaminase	S4VYT2	Pandoravirus	5.8e-10	31.4
WP_168571198.1\|5663240_5663657_-	DUF393 domain-containing protein	NA	NA	NA	NA
WP_168571199.1\|5663715_5664033_-	glutaredoxin 3	V9QKN6	Rhizobium_phage	1.2e-10	45.5
WP_168572028.1\|5664465_5664984_-	mechanosensitive ion channel	NA	NA	NA	NA
WP_168571200.1\|5665237_5667850_-	CHAT domain-containing protein	NA	NA	NA	NA
WP_168571201.1\|5667801_5669658_-	ShlB/FhaC/HecB family hemolysin secretion/activation protein	NA	NA	NA	NA
WP_168571202.1\|5670148_5670850_-	Uma2 family endonuclease	NA	NA	NA	NA
WP_168571203.1\|5670891_5672310_-	cobyrinate a,c-diamide synthase	NA	NA	NA	NA
WP_168571204.1\|5672834_5674670_+	VWA domain-containing protein	NA	NA	NA	NA
WP_168571205.1\|5674980_5675139_+	hypothetical protein	NA	NA	NA	NA
WP_168571206.1\|5675204_5676671_+	multicopper oxidase family protein	NA	NA	NA	NA
WP_168571207.1\|5677159_5677756_+	zinc ribbon domain-containing protein	NA	NA	NA	NA
WP_168571208.1\|5677898_5678672_+	class I SAM-dependent methyltransferase	NA	NA	NA	NA
WP_168571209.1\|5678798_5681894_+	transglutaminase family protein	NA	NA	NA	NA
WP_168571210.1\|5682715_5682931_+	DUF4327 family protein	NA	NA	NA	NA
WP_168571211.1\|5683699_5685460_+\|protease	M48 family metalloprotease	NA	NA	NA	NA
WP_168571212.1\|5685725_5686394_-\|protease	ATP-dependent Zn protease	NA	NA	NA	NA

DBSCAN-SWA_6

6249989 : 6307045

Ostreococcus_lucimarinus_virus(16.67%)

holin,tRNA,transposase

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_168571594.1\|6249989_6250364_+\|holin	phage holin family protein	NA	NA	NA	NA
WP_168571595.1\|6250596_6250788_-	hypothetical protein	NA	NA	NA	NA
WP_168571596.1\|6250750_6253087_-	hypothetical protein	NA	NA	NA	NA
WP_168571597.1\|6254759_6256187_-	decarboxylating NADP(+)-dependent phosphogluconate dehydrogenase	A0A0P0C6S9	Ostreococcus_lucimarinus_virus	2.7e-41	29.0
WP_168571598.1\|6256412_6257627_-\|transposase	IS200/IS605 family element transposase accessory protein TnpB	A0A7P9	Microcystis_virus	2.3e-113	59.9
WP_168571599.1\|6258046_6259786_+	hypothetical protein	NA	NA	NA	NA
WP_168571600.1\|6259981_6261208_+\|transposase	IS200/IS605 family element transposase accessory protein TnpB	A0A0H3UZC2	Geobacillus_virus	6.5e-76	43.5
WP_168571601.1\|6262917_6266289_+\|tRNA	isoleucine--tRNA ligase	A0A2P1ELB8	Moumouvirus	2.0e-79	28.2
WP_168571602.1\|6266366_6267725_+	DUF3696 domain-containing protein	Q2P9X8	Enterobacteria_phage	3.2e-23	30.7
WP_168572072.1\|6267736_6268213_+	hypothetical protein	NA	NA	NA	NA
WP_168571603.1\|6268337_6269021_-	HEAT repeat domain-containing protein	NA	NA	NA	NA
WP_168571604.1\|6269121_6269721_-	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_168571605.1\|6270006_6271584_+	hypothetical protein	NA	NA	NA	NA
WP_168571606.1\|6271580_6276293_-	PAS domain S-box protein	Q8QKV7	Ectocarpus_siliculosus_virus	7.3e-43	30.6
WP_168571607.1\|6278015_6278942_+	TIGR01777 family protein	NA	NA	NA	NA
WP_168571608.1\|6279329_6279521_+	hypothetical protein	NA	NA	NA	NA
WP_168571609.1\|6279631_6280012_-	hypothetical protein	NA	NA	NA	NA
WP_168572073.1\|6280125_6280926_+	PEP-CTERM sorting domain-containing protein	NA	NA	NA	NA
WP_168571610.1\|6281074_6282280_-	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_168571611.1\|6282412_6282736_-	DUF3082 domain-containing protein	NA	NA	NA	NA
WP_168571612.1\|6282781_6283726_-	4-(cytidine 5'-diphospho)-2-C-methyl-D-erythritol kinase	NA	NA	NA	NA
WP_168571613.1\|6283734_6284577_-	16S rRNA (adenine(1518)-N(6)/adenine(1519)-N(6))- dimethyltransferase RsmA	NA	NA	NA	NA
WP_168571614.1\|6284659_6285295_-	triacylglycerol lipase	NA	NA	NA	NA
WP_168571615.1\|6285638_6286076_+	hypothetical protein	NA	NA	NA	NA
WP_168571616.1\|6286399_6286603_-	hypothetical protein	NA	NA	NA	NA
WP_168571617.1\|6286662_6287844_+	calcium-binding protein	NA	NA	NA	NA
WP_168571618.1\|6287994_6292002_+	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_168571619.1\|6292175_6293354_+	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_168571620.1\|6293609_6294143_-\|transposase	transposase	NA	NA	NA	NA
WP_168572074.1\|6294811_6297139_-	glycosyltransferase	NA	NA	NA	NA
WP_168571621.1\|6297259_6299644_-	glycosyltransferase family 4 protein	NA	NA	NA	NA
WP_168571696.1\|6299888_6300908_-\|transposase	IS4 family transposase	NA	NA	NA	NA
WP_168571622.1\|6301245_6302538_+	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_168571623.1\|6302970_6306138_-	UbiA family prenyltransferase	NA	NA	NA	NA
WP_168571624.1\|6306469_6307045_-\|transposase	transposase	NA	NA	NA	NA

Anti-CRISPR protein detection

Acr ID	Acr position	Acr size	Homology with known anti	Neighbor HTH/AcRanker	Neighbor Aca	In prophage	Protospacer in prophage

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP051167

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CRISPR-Cas detection and classification

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Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection