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_CP043618	Sulfurimonas sp. GYSZ_1 plasmid unnamed, complete sequence	0 crisprs	NA	0	0	0	0
NZ_CP043617	Sulfurimonas sp. GYSZ_1 chromosome, complete genome	4 crisprs	DEDDh,RT,WYL,csa3,cas3,cas9,cas1,cas2	1	20	1	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP043617_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP043617_1

13990-14093

Orphan

Consensus_repeat	Method
AATAAGCAGTTATTATTTGCTTTAC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP043617_1

>merge|NZ_CP043617|1|13990-14093|CRISPRCasFinder
AATAAGCAGTTATTATTTGCTTTACTATTTAGTCCTCGATGGTCCTTCGGACAACATCTGCGGTTCCGAACCTACAAATAATAAGCAGTTATTATTTGCTTTAC

>NZ_CP043617|1|1|13990-14093|CRISPRCasFinder
AATAAGCAGTTATTATTTGCTTTAC	TATTTAGTCCTCGATGGTCCTTCGGACAACATCTGCGGTTCCGAACCTACAAAT
AATAAGCAGTTATTATTTGCTTTAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP043617.1\|WP_152306146.1\|14978_16055_-\|23S-rRNA-(adenine(2503)-C(2))-methyltransferase-RlmN	unknown	unknown	gnl\|CDD\|237719
NZ_CP043617.1\|WP_152306148.1\|16715_17474_-\|imidazole-glycerol-phosphate-synthase-subunit-HisF	unknown	unknown	gnl\|CDD\|234996
NZ_CP043617.1\|WP_152306153.1\|21592_22897_+\|flagellar-protein-export-ATPase-FliI	unknown	unknown	gnl\|CDD\|181439
NZ_CP043617.1\|WP_152306140.1\|8331_8715_-\|flagellar-assembly-protein-FliW	unknown	unknown	gnl\|CDD\|183946
NZ_CP043617.1\|WP_152306142.1\|9075_11442_-\|ribonucleoside-diphosphate-reductase-subunit-alpha	unknown	unknown	gnl\|CDD\|236266
NZ_CP043617.1\|WP_152306147.1\|16051_16594_-\|purine-nucleoside-phosphorylase	unknown	unknown	gnl\|CDD\|376443
NZ_CP043617.1\|WP_152306137.1\|3312_5052_-\|response-regulator	unknown	unknown	gnl\|CDD\|274362
NZ_CP043617.1\|WP_152308338.1\|6416_6839_-\|thioredoxin-TrxC	unknown	unknown	gnl\|CDD\|182889
NZ_CP043617.1\|WP_152306149.1\|17655_18120_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379331
NZ_CP043617.1\|WP_152306143.1\|11650_12979_-\|adenylosuccinate-lyase	unknown	unknown	gnl\|CDD\|181437
NZ_CP043617.1\|WP_152306150.1\|18162_18948_+\|16S-rRNA-(adenine(1518)-N(6)/adenine(1519)-N(6))--dimethyltransferase-RsmA	unknown	unknown	gnl\|CDD\|234708
NZ_CP043617.1\|WP_152306145.1\|14573_14819_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP043617.1\|WP_152306141.1\|8735_9074_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP043617.1\|WP_152306154.1\|22900_25018_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238121
NZ_CP043617.1\|WP_152306138.1\|5077_6355_-\|citrate-synthase	unknown	unknown	gnl\|CDD\|180164
NZ_CP043617.1\|WP_152306152.1\|21002_21587_+\|GTP-cyclohydrolase-I-FolE	unknown	unknown	gnl\|CDD\|236472
NZ_CP043617.1\|WP_152306151.1\|18962_20912_+\|RNase-J-family-beta-CASP-ribonuclease	unknown	unknown	gnl\|CDD\|223668
NZ_CP043617.1\|WP_152306135.1\|1567_2812_+\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|226229
NZ_CP043617.1\|WP_152306139.1\|6838_8218_-\|Do-family-serine-endopeptidase	unknown	unknown	gnl\|CDD\|273938
NZ_CP043617.1\|WP_152306136.1\|2821_3316_+\|crossover-junction-endodeoxyribonuclease-RuvC	unknown	unknown	gnl\|CDD\|234587

Protein	Function_ID	Function_description	E-value
NZ_CP043617.1\|WP_152306146.1\|14978_16055_-\|23S-rRNA-(adenine(2503)-C(2))-methyltransferase-RlmN	gnl\|CDD\|237719	PRK14462, PRK14462, 23S rRNA (adenine(2503)-C(2))-methyltransferase RlmN.	0
NZ_CP043617.1\|WP_152306148.1\|16715_17474_-\|imidazole-glycerol-phosphate-synthase-subunit-HisF	gnl\|CDD\|234996	PRK02083, PRK02083, imidazole glycerol phosphate synthase subunit HisF; Provisional.	5.78948e-170
NZ_CP043617.1\|WP_152306153.1\|21592_22897_+\|flagellar-protein-export-ATPase-FliI	gnl\|CDD\|181439	PRK08472, fliI, flagellar protein export ATPase FliI.	0
NZ_CP043617.1\|WP_152306140.1\|8331_8715_-\|flagellar-assembly-protein-FliW	gnl\|CDD\|183946	PRK13282, PRK13282, flagellar assembly protein FliW; Provisional.	4.49333e-46
NZ_CP043617.1\|WP_152306142.1\|9075_11442_-\|ribonucleoside-diphosphate-reductase-subunit-alpha	gnl\|CDD\|236266	PRK08447, PRK08447, ribonucleoside-diphosphate reductase subunit alpha.	0
NZ_CP043617.1\|WP_152306147.1\|16051_16594_-\|purine-nucleoside-phosphorylase	gnl\|CDD\|376443	pfam01048, PNP_UDP_1, Phosphorylase superfamily. Members of this family include: purine nucleoside phosphorylase (PNP) Uridine phosphorylase (UdRPase) 5'-methylthioadenosine phosphorylase (MTA phosphorylase).	4.59914e-07
NZ_CP043617.1\|WP_152306137.1\|3312_5052_-\|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].	1.10574e-84
NZ_CP043617.1\|WP_152308338.1\|6416_6839_-\|thioredoxin-TrxC	gnl\|CDD\|182889	PRK10996, PRK10996, thioredoxin 2; Provisional.	8.50473e-52
NZ_CP043617.1\|WP_152306149.1\|17655_18120_+\|hypothetical-protein	gnl\|CDD\|379331	pfam13682, CZB, Chemoreceptor zinc-binding domain. The chemoreceptor zinc-binding domain (CZB) is found in bacterial signal transduction proteins - most frequently receptors involved in chemotaxis and motility, but also in c-di-GMP signalling and nitrate/nitrite-sensing. Originally discovered in the cytoplasmic chemoreceptor TlpD from Helicobacter pylori, it is often found C-terminal to the MCPsignal domain in cytoplasmic chemoreceptor proteins. The CZB domain contains a core sequence motif, Hxx[WFYL]x21-28Cx[LFMVI]Gx[WFLVI]x18-27HxxxH. The highly-conserved H-C-H-H residues of this motif are believed to coordinate zinc; mutating the latter two histidines of the motif to alanines abolishes Zn binding. This domain binds zinc with high affinity, with a Kd in the femtomolar range. This domain has been shown in E. coli to be a zinc sensor that regulates the catalytic activity of pfam00990.	1.92418e-08
NZ_CP043617.1\|WP_152306143.1\|11650_12979_-\|adenylosuccinate-lyase	gnl\|CDD\|181437	PRK08470, PRK08470, adenylosuccinate lyase; Provisional.	0
NZ_CP043617.1\|WP_152306150.1\|18162_18948_+\|16S-rRNA-(adenine(1518)-N(6)/adenine(1519)-N(6))--dimethyltransferase-RsmA	gnl\|CDD\|234708	PRK00274, ksgA, 16S rRNA (adenine(1518)-N(6)/adenine(1519)-N(6))-dimethyltransferase RsmA.	4.21963e-86
NZ_CP043617.1\|WP_152306154.1\|22900_25018_-\|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.	5.79181e-06
NZ_CP043617.1\|WP_152306138.1\|5077_6355_-\|citrate-synthase	gnl\|CDD\|180164	PRK05614, gltA, citrate synthase.	0
NZ_CP043617.1\|WP_152306152.1\|21002_21587_+\|GTP-cyclohydrolase-I-FolE	gnl\|CDD\|236472	PRK09347, folE, GTP cyclohydrolase I; Provisional.	5.04508e-117
NZ_CP043617.1\|WP_152306151.1\|18962_20912_+\|RNase-J-family-beta-CASP-ribonuclease	gnl\|CDD\|223668	COG0595, COG0595, mRNA degradation ribonucleases J1/J2 (metallo-beta-lactamase superfamily) [Translation, ribosomal structure and biogenesis; Replication, recombination and repair].	0
NZ_CP043617.1\|WP_152306135.1\|1567_2812_+\|diguanylate-cyclase	gnl\|CDD\|226229	COG3706, PleD, Response regulator containing a CheY-like receiver domain and a GGDEF domain [Signal transduction mechanisms].	1.01229e-76
NZ_CP043617.1\|WP_152306139.1\|6838_8218_-\|Do-family-serine-endopeptidase	gnl\|CDD\|273938	TIGR02037, Probable_periplasmic_serine_protease_do/HhoA-like, periplasmic serine protease, Do/DeqQ family. This family consists of a set proteins various designated DegP, heat shock protein HtrA, and protease DO. The ortholog in Pseudomonas aeruginosa is designated MucD and is found in an operon that controls mucoid phenotype. This family also includes the DegQ (HhoA) paralog in E. coli which can rescue a DegP mutant, but not the smaller DegS paralog, which cannot. Members of this family are located in the periplasm and have separable functions as both protease and chaperone. Members have a trypsin domain and two copies of a PDZ domain. This protein protects bacteria from thermal and other stresses and may be important for the survival of bacterial pathogens.// The chaperone function is dominant at low temperatures, whereas the proteolytic activity is turned on at elevated temperatures. [Protein fate, Protein folding and stabilization, Protein fate, Degradation of proteins, peptides, and glycopeptides].	3.36997e-165
NZ_CP043617.1\|WP_152306136.1\|2821_3316_+\|crossover-junction-endodeoxyribonuclease-RuvC	gnl\|CDD\|234587	PRK00039, ruvC, Holliday junction resolvase; Reviewed.	6.54328e-74

>NZ_CP043617.1|WP_152306143.1|11650_12979_-|adenylosuccinate-lyase
MVERYAREEMSKNWTQHARYAAWLEVEKAAVKAWAKLGKIPQDDADKIVKNATFSVERIEEIEAITKHDLIAFNTSVSESLGDESRWFHYGMTSSDAVDTGVALQMRDSLTIIIEDVKMLMESIKKRAEEHKFTLMVGRSHGIHGEPITFGLTLAVWYDEVARHLKNLEDTMEVISVGQISGAMGNFAHAPLELEELAMAELGLKPEPCSNQVVHRDRYARLATALALLASSVEKFAVQVRHLQRTEVYEAEEYFAKGQKGSSAMPHKRNPILTENITGLARMIRAYANPAMENVALWHERDISHSSTERFWLPDAFITTDFMLHRMNSVIANLTVMPENMMKNLNLTGGLVFSQRVLLELPLQGVSREDAYKIVQRNAMKVWEEIQQGKATTNEKGESLYLNHLLADDELRSKLSEEQIRECFNYDYYTKNVDAIFKRVFG
>NZ_CP043617.1|WP_152306142.1|9075_11442_-|ribonucleoside-diphosphate-reductase-subunit-alpha
MITVIKRNGRTEPLDITKIQKYTSAAVKGLENVSQSELEVDAQIHFRDGITSKEIQQTLIKTAVDKIDIDAPNWTFVASRLFMFNLYHQVNGFSGYSSLEDYFKRGEKEGRLLLGLKEMYDLEALDKHIKPERDMLFNYLGVKTLYDRYLIKDRNSDPIELPQHMFMAIAMFLAQREENRQEWAIKFYDMISQFEVMLATPTLSNARTTRHQLSSCYIGSTPDNIEGIFDSYAEMAMLSKFGGGIGWDWTQVRSMGSYIDGHKNAAGGTVPFLKITNDIAIAVDQLGTRKGAIAVYLEPWHIDINDFLDLKKNSGEERRRAHDLFPSLWLNDLFMQRVQEDGIWTLFDPYDVRELSTLHGEEFSKRYIELENDEGLIKEKIKAKNLWKKILTSYFETGSPFLCFKDNANRANPNSHTGVIRSSNLCTEIFQNTNPNRYKIKFIFENGDSVSYEEDEIVKVDSGIEKPAKKVTALDSLGGMPIYVVEKEKINGDTAVCNLASVNLSRINTKEDIDRIVPTAIRCLDNVIDLNFYPVEKVKRTNMKTRSIGLGVMGEAQMLAEAGITWGSQEHFDKIDEIMESVSFNAISASSDLAIEKGQYPEFEGSKWSQGIMPHDHANAEVVNLVDRGGLFASKYEWDDLRAKVKKQGMRNGYLMAVAPTSSISILTGTTQAIEPVFKRKWFEENLSGLIPVVVPKLSPETWAFYTPAYDLNQTILIKAAAIRQKWIDQGQSLNIFITLDKASGKYLNEIYMLAWKLGLKSTYYLRSQSPEISNDVEDRSMECVGCQ
>NZ_CP043617.1|WP_152306141.1|8735_9074_-|hypothetical-protein
MKPLSKNSLENFLKRFEYFKDGEFRDIIINSPTNITLNFAIQDASRGYDWITLKLEFDGISDASLLDSSNLAHIDMSEGVYLKNDGTEFAFKVNNSTFKIKSSSLKYEEGQF
>NZ_CP043617.1|WP_152306140.1|8331_8715_-|flagellar-assembly-protein-FliW
MSYEVKGQILGFENTMTVDIHEVDELFSTMIDVNNENISFTLANPYVLREYSFDLPTNLKVLLDIKEDSKVNVYNIVVIQEPLEKSSVNFLAPIIVNEDNKTVGQAVLNSKTHPDFGMAETIESFKQ
>NZ_CP043617.1|WP_152306139.1|6838_8218_-|Do-family-serine-endopeptidase
MKKIALVLLLGLSLLQAKGSIDFKYSDVETRKFPTNQDYILSYNNVLKDVRTSVVNISTQKNVTQTVNPLMNDPFFREFFRGYQNIPQERIQRALGSGVIISEDGYIVTNNHVVDGADKIVVNLVGDKKEYEAKLIGKDEKSDLAVIKIEKDDLNAVSFYNSDNVKVGDVVFALGNPFGLHETITQGIVSATGRSGVGIVEYENFIQTDASINPGNSGGALINSKGDLIGINSAILSKSGGNVGIGFAIPSNMVTSIAKQLIESGKFSRAYLGVNISDISEDMSKFYNNNFGALVTGVEDETPAQKAGIIRGDLIVAVNSKEIKSASELKNIIGTFAPNTEVTIKFLRDKKLKTAEVKLGSLENISPSGAVSYNGIELRDIDAQTRSRLMLSQEVKGVIVTKVDPKSDAARIGVKIGDVVIQVENKEITNTKEFLHATKSKSKKRLFIYRRGGVFAVVL
>NZ_CP043617.1|WP_152308338.1|6416_6839_-|thioredoxin-TrxC
MRVVCPHCLSVNNIPKKESYKKANCGKCKKSLLDTNPIELTDSNFDEVVVNSDIPVIVDFWAPWCGPCKMFGPVFEKSSKNYPLKALYVKVNTENEQNLGARFGIRSIPTLMIFKNSKEAHRISGALDESSLNNLVSQFT
>NZ_CP043617.1|WP_152306138.1|5077_6355_-|citrate-synthase
MAKNTVTIINNRDGKEYEFNILDASIGPSVVDISSFYKETGMFTYDEGYTSTASCESKITYIDGAAGKLMYRGYDISYMAKEKSFLDTAYLLLNGELPTKEESKEFRIEMNKRAFVHEGIRKLYDSFPDRAHPMAILSAGVSALSTIYFNHLEINTPEEYREMANRIVAKVPTLAAMSYRYSNGMPIIYPDLDKTFTENFLYMMRAYPHKHVDLKPIEVKALDTIFTLHADHEQNASTTAVRNLASTMAHPYAAISAGIGALWGRSHGGANESVIRQLEMIGTVDKVDEFIARAKDKNDPFRLMGFGHRVYKNFDPRATILKDIRDKLMDELGISSELVAVANKIEHIALNDEYFVSRGLYPNIDFYSGLILRALKIPKEMFAVIFVIGRTPGWIAQWSELRQQKTIKIARPRQLYTGKTERTPN
>NZ_CP043617.1|WP_152306137.1|3312_5052_-|response-regulator
MEKKDYLEHKELAYLYDNLNSSTLGLFGVATVIFFVLRGEVPDINLNIWYLFIVFMVIARLFLAKKYSSVKINKKNFKKYKFYFAISLITSGTVWGVIPFVILPQSIVYQIFLVLMLGGLTSTASASLATNNKLYISFVILTMTPFMYIITTMDNPIYNPLFITLFLYILFSFASSKKMNKLVINSISLSYRNQDLIKKLEVKADEANRAAEAKSNFLSTMSHEIRTPLNAIIGFIKILKKTEKDSKRLKYLNTIDQSSYSLLNIINDILDFSKIESGKFSLEFTKFNPKKELDNIYELYSEAASENGVTLVNSISNKLPKNIKTDKLRLKQIISNLISNAIKFTHENNEVEFIVKFNRAESSLYIEIKDEGIGIEKEKISSITQEFIQADTSITRKYGGTGLGLSIVLKLLKLLGSELHIESELGKGSRFFFTIDIEVLDSNEEELTTTEDIHRFENKSILVVEDNKTNQMLIKLLLDDMDIDITMANDGLEAENYFKKEKYDMVFMDINMPNKNGLEAMKSIKEYQKDFENKTPIIALTANAVSGDREKYIEEGFDDYLAKPINNESLITILKKYLD
>NZ_CP043617.1|WP_152306136.1|2821_3316_+|crossover-junction-endodeoxyribonuclease-RuvC
MIILGIDPGTRNMGYALIELNKGKTSLKEAGLIKIKADDLQFQIPQMVEAFDTIFKNNKIDEVAMEDIFYAHNPKTTIKLAQFRGAIMLKLLQEFGQFSEYTALQVKQAITGNGKAKKEQVAFMVKRLLNIKKEIKPLDITDAIAVAITHSQRIKFSENKKSTT
>NZ_CP043617.1|WP_152306135.1|1567_2812_+|diguanylate-cyclase
MDRILVIEDNKTLANLMAKKISSKLDFEVDVAYSMSEAKLFLKGYKYFLTLSDLNLPDAPNGEIIDYVLKTGNHVIILTSNIDKSFRKKMFEKNIIDYIHKTGIEDINYIINNIRRLSKNRKHKVLVVDDSVVFRKQMKDMLTNLFFNVITVAHGEEAINILDTTPDISLVLTDYNMPVMNGLELTTQIRKKYKKSELCIIALSGKSDDEEIAMFLKSGANDFIKKPFSKEEFSCRINNSIEALENIHAITNQSIRDFLTGLYNRRYFFKEVEKYFIDAVNNDESFSIAMVDIDDLKKINDTYGHENGDKIIVSLAETLRSETSKDDIVARFGAGEFCMVLKDVSTDKAIDALESIRQKVQNSVTLSDKNQEIKYTISVGIALEHENTLEDTVNEADMHLYTAKENGKNKIEHQ
>NZ_CP043617.1|WP_152306145.1|14573_14819_-|hypothetical-protein
MSDIPKKTNTERIKRIYDLCEEHFGDIRFVGIKYHKKIGWIAKAQFDDGFENLTADGETSVEALRKLKKRVKKIINRYNKV
>NZ_CP043617.1|WP_152306146.1|14978_16055_-|23S-rRNA-(adenine(2503)-C(2))-methyltransferase-RlmN
MTELKPSLLDFTKKELLDIIKPSFRVKQILGWLYHNYASEYDDMKNIPKSLKEELAKKYIVNPLKIIKKEVSSDGTVKYLFELQDGKTVEAVWLKMKDDVYDESGKLIHEAKYTICVSTQVGCKVGCAFCLTAKGGFTRDLSAGEIVGQVVALKRDNAHKHNRKINIVYMGMGEPLDNLNNLAKAIEIFKEEDGLSISGKRQTVSTSGLSNKIDQLGAMDLGVHIAISLHAVDDELRTELIPMNKAHNINSIIEAVKRFPIDTRKRVMFEYLVIKDKNDDLASAKKLVKLLHGIKAKVNLIYFNPYPGTTYNRPELKDMLNFQEYLVKHGLLCTIRDSKGIDISAACGQLKEKNKEIS
>NZ_CP043617.1|WP_152306147.1|16051_16594_-|purine-nucleoside-phosphorylase
MIICAGNNETFDFATPMGVGLIESAMNITRLCLFDKPEFLLFVGTAGSYGKHEIFDIIESKTASNIELGFLDSCAYTPLDNVVSTNTTNTQDIIVNSSNYISTCKEQTKKFLKFGVEIENMEFYSVLKIAQEFNIPAGGVFCVTNYTNKNAHKDFLDNHTKAKELLTEHVKKRIKELTSV
>NZ_CP043617.1|WP_152306148.1|16715_17474_-|imidazole-glycerol-phosphate-synthase-subunit-HisF
MNYFAKRIIPCLDVKDGRVVKGVNFVGLKDAGDPVEVAKRYNQEGADEITFLDITASSDNRDTIVDIVAEVAREIFIPLTVGGGIRKLDDIYKLLNVGCDKVSVNSAAIKRPELINEGAKRFGSQCIVTAIDVKKTGDSYNVYLNGGRVDTGIDAVEWAKEVVDRGSGEILLTSMDADGTKAGFELNITEQISSVVNVPVIASGGAGTMEHIKDAFNHGADAALAASIFHYKEIDIMDLKHYLNDEGIAVRL
>NZ_CP043617.1|WP_152306149.1|17655_18120_+|hypothetical-protein
MDKEEIIEHLRAAKTAHIKWVQKAKLLINGIEIEKDAIPVNSTECKFGKWFYSDGQVLNALSNNPMECMNSIEQLHFELHDIYMHIFNIYFSKPEGGFLSKLFGKKKEVTEIDAQRAQTYFANMEEVSKKLLDEINRLERRILAIPEERIKELM
>NZ_CP043617.1|WP_152306150.1|18162_18948_+|16S-rRNA-(adenine(1518)-N(6)/adenine(1519)-N(6))--dimethyltransferase-RsmA
MNENSVVAKKKFGQNFLKDESVLHKIIQSKPKNDNKIVEIGPGLGDLTKYLVDVGSVEAFEVDTDLCKILQEKFKKEINTKQLHLNCGDVLNAWQSSSEGNLIDEPYDLVANLPYYIATNIILKALADTMCKNILVMTQLEVAEKFCAEAGEKVFGSLGIITQSVGTAKIVVKVPPTAFEPPPKIDSAVFLIQKDKDRSDKAFEDMLRVAFMQPRKTLMKNLSSKYEKAKLQEVFQELGLTLTIRPHQVNTKDYHQLYKKI
>NZ_CP043617.1|WP_152306151.1|18962_20912_+|RNase-J-family-beta-CASP-ribonuclease
MEKNGNVKEPEVNGNVKESSKPNSNRKPNNRNNNRSNQNRDSKQNNKNNSQNRNKNSGGRGRRRQSTPVDENLKKFVAMNQEGHKQRLNPHFKLDLNSKDKIRITPLGGLGEIGGNITVFETQKEAILVDVGMSFPDEDMHGVDILVPDFSYIREIKDKIKAVIITHAHEDHIGAMPYLYKEMQFPIYGSPLPLAMIGNKFDEHHIKEHRRFFNPIEKRKVYEIGDDFKIEWMHMTHSIIDSSSLAITTEAGTVIHTGDFKIDHTPVDGYTADLHRLAYYGEKGVLCLLSDSTNSYNPQPTPSELSVAPALDRVFSKAEGRVILSTFSSNIHRVQQAIQYGIKYGRKICVIGRSMERNIEIAMQYDYVKLPKNAFVEPEQISHMNDKDVLIVTTGSQGEPSSALFRMSIGEHRHVKIKPTDLVVLSSRAIPGNEGSISGMLNHLQRAGAKISHDKDIHVSGHASIEEQKLMLRLTNPKFFLPVHGEYNHVVRHKETAVMCGIPERNIYIMNDGDSIEVAPKYMRKVKTVKSGKTYIDNQNNHKIDDDIVLDRQKLASDGIVMLIAEVDGQHAKMLSKPKVTTFGLVADKQDKAFAKEMEDVLEHFLLHIKDGLLENGRALENDLRQVVRKHIYRKMKKYPLIVPHVFVQ
>NZ_CP043617.1|WP_152306152.1|21002_21587_+|GTP-cyclohydrolase-I-FolE
MSDTKDTQFENAVKTMMEHVGEDPNREGLLDTPSRVKKAYEFIFGGYKEDPKKILESALFTSSNDEMVLIKDIELYSTCEHHLLPIIGRVHVAYIPDGKVVGLSKIPRVVNVFARRMQIQEQLTEQIADAIMETINPKGVAVVVQARHMCMEMRGVEKINSTTTSSALRGLFKKDEKTRGEFFSLINSPTGTRY
>NZ_CP043617.1|WP_152306153.1|21592_22897_+|flagellar-protein-export-ATPase-FliI
MPFSSLKEKLSSVSHSTHFGEVVKINATVITATGLNVSISDMVKIISNYNGQETVGMVTEIDGNTFYITPFRFVEGFRAGDKVYLDSNGLNINVGEGLIGRVVNPFMQPIDGKGPIKNTQTAPIIKEPIPAMKRGMIDEVFSVGVKSIDGLLTCGKGQKLGIFAGSGVGKSTLMGMIVRGADAPVKVVALIGERGREVPEFIEKNLGGDLTNTVIIVATSDDSPLMRKYGAFSAMSVAEYFKDKGQDVLFIMDSVTRFAMAQREIGLALGEPPTSKGYPPSSLTLLPQLMERAGKEVGKGSITAFFTVLIEGDDMSDPIADQSRSILDGHIVLSRELTDFGIYPPIHILNSASRVMNDITSVEHIDAVMKFRRMYTLLKENEMLIRIGAYIKGTDKELDEAIEKKDSMENFLKQRADNQIPYEQSMQEILSIIK
>NZ_CP043617.1|WP_152306154.1|22900_25018_-|hypothetical-protein
MSEIIECIKARSFITSLKTTSTDELAFCTKLHGAKIFSTKNCNVKYHFTSQHLNQDTTAFTFNLQGNLIAFANIKAIYIADIEKKEILKIIPTDDQHIQILTFDETSNYLIAGNENGRVTQYNWANSSAISRLCSFPHECSDRKYIRKNYVSALCVKNNRLACSGLGGAIIVLDMYSRANKIVLQNTNSRINALHFIDDDTILSANFDGLISIFSIKQRKLLSEIDTPLTQIRQVLPMPESNYIMLCSNTNYVSIVDIKNSKMLQHKYMSFDDKVIRLSSIDYKHVAVALRSGFIKKIELSCEEDLKSLVLHNSLDKAYELVEKEPMLKSTKTYMDLNKLYNNIYNKAIVALINQNTSLANELLKMFKNIPSKQKEINSLFIAFKNYNNLKLLYLSKKLSLAYALCSKYPELEKTPIFRKMEEIWRDVFKNAQRQILLNKTQNARSLLQEYKTIPSKKEMIDLVLNQNKDFVEFIFAIDKKNYAKASMLALRNKLLMKSPSYNTLQSEIEYKTEQIKNFIYHGDVANARIAISIIKDVPYLKQQISDFDRECKHLEALQHYYKENNLKKCYETLDIYTSLYTTELGELLEKHWQKIVEECESYALKGKISDIKNTLGLLVTLKSRVDKIGDLFRLAFHIRVKTYLSKRSFKNAQQLIYSYIDTFGLDYEIKMLMKKYEQKTKHKLAITHDITTQRDSWLFSEFIQ

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP043617_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP043617_2

553654-553739

Orphan

Consensus_repeat	Method
ATTATTCTCATAATAATTTATTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP043617_2

>merge|NZ_CP043617|2|553654-553739|CRISPRCasFinder
ATTATTCTCATAATAATTTATTTAAAAATAATACTATTGAAAAGTCAAGAGACATTACTCTTGATTATTCTCATAATAATATATTT

>NZ_CP043617|2|2|553654-553739|CRISPRCasFinder
ATTATTCTCATAATAATTTATTT	AAAAATAATACTATTGAAAAGTCAAGAGACATTACTCTTG
ATTATTCTCATAATAATATATTT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP043617.1\|WP_152306676.1\|561981_562578_+\|branched-chain-amino-acid-aminotransferase	unknown	unknown	gnl\|CDD\|235934
NZ_CP043617.1\|WP_152306664.1\|552193_552664_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377526
NZ_CP043617.1\|WP_152306657.1\|546347_547559_+\|nitrous-oxide-reductase-family-maturation-protein-NosD	unknown	unknown	gnl\|CDD\|275079
NZ_CP043617.1\|WP_152306671.1\|557029_558112_+\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP043617.1\|WP_152306660.1\|548889_549369_+\|c-type-cytochrome	unknown	unknown	gnl\|CDD\|225418
NZ_CP043617.1\|WP_152306662.1\|550286_550925_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP043617.1\|WP_152306661.1\|549378_550284_+\|NapH/MauN-family-ferredoxin-type-protein	unknown	unknown	gnl\|CDD\|274004
NZ_CP043617.1\|WP_152306659.1\|548276_548888_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225418
NZ_CP043617.1\|WP_152306658.1\|547561_548302_+\|4Fe-4S-dicluster-domain-containing-protein	unknown	unknown	gnl\|CDD\|319895
NZ_CP043617.1\|WP_152306663.1\|551357_552185_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|372253
NZ_CP043617.1\|WP_152306672.1\|558115_558790_+\|response-regulator	unknown	unknown	gnl\|CDD\|223816
NZ_CP043617.1\|WP_152306665.1\|552665_553190_+\|PAS-domain-containing-protein	unknown	unknown	gnl\|CDD\|369881
NZ_CP043617.1\|WP_152308365.1\|551019_551358_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP043617.1\|WP_152306670.1\|556062_557028_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP043617.1\|WP_152306675.1\|561062_561992_+\|cysteine-synthase-A	unknown	unknown	gnl\|CDD\|273463
NZ_CP043617.1\|WP_152306674.1\|560607_561051_+\|low-molecular-weight-phosphotyrosine-protein-phosphatase	unknown	unknown	gnl\|CDD\|319971
NZ_CP043617.1\|WP_152306668.1\|554956_555394_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP043617.1\|WP_152306667.1\|554415_554853_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377526
NZ_CP043617.1\|WP_152306673.1\|558776_560474_-\|nitrite/sulfite-reductase	unknown	unknown	gnl\|CDD\|223233
NZ_CP043617.1\|WP_152306669.1\|555403_556066_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|223736

Protein	Function_ID	Function_description	E-value
NZ_CP043617.1\|WP_152306676.1\|561981_562578_+\|branched-chain-amino-acid-aminotransferase	gnl\|CDD\|235934	PRK07101, PRK07101, hypothetical protein; Provisional.	7.80355e-77
NZ_CP043617.1\|WP_152306664.1\|552193_552664_+\|hypothetical-protein	gnl\|CDD\|377526	pfam05573, NosL, NosL. NosL is one of the accessory proteins of the nos (nitrous oxide reductase) gene cluster. NosL is a monomeric protein of 18,540 MW that specifically and stoichiometrically binds Cu(I). The copper ion in NosL is ligated by a Cys residue, and one Met and one His are thought to serve as the other ligands. It is possible that NosL is a copper chaperone involved in metallo-centre assembly.	3.48485e-18
NZ_CP043617.1\|WP_152306657.1\|546347_547559_+\|nitrous-oxide-reductase-family-maturation-protein-NosD	gnl\|CDD\|275079	TIGR04247, nitrous_oxide_maturation_protein_NosD, nitrous oxide reductase family maturation protein NosD. Members of this family include NosD, a repetitive periplasmic protein required for the maturation of the copper-containing enzyme nitrous-oxide reductase. NosD appears to be part of a complex with NosF (an ABC transporter family ATP-binding protein) and NosY (a six-helix transmembrane protein in the ABC-2 permease family). However, NosDFY-like complexes appear to occur also in species whose copper requiring enzymes are something other than nitrous-oxide reductase.	3.21107e-159
NZ_CP043617.1\|WP_152306671.1\|557029_558112_+\|PAS-domain-S-box-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	3.66452e-34
NZ_CP043617.1\|WP_152306662.1\|550286_550925_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	1.19259e-58
NZ_CP043617.1\|WP_152306660.1\|548889_549369_+\|c-type-cytochrome	gnl\|CDD\|225418	COG2863, COG2863, Cytochrome c553 [Energy production and conversion].	4.93132e-13
NZ_CP043617.1\|WP_152306661.1\|549378_550284_+\|NapH/MauN-family-ferredoxin-type-protein	gnl\|CDD\|274004	TIGR02163, Ferredoxin-type_protein_NapH_homolog, ferredoxin-type protein, NapH/MauN family. Most members of this family are the NapH protein, found next to NapG,in operons that encode the periplasmic nitrate reductase. Some species with this reductase lack NapC but accomplish electron transfer to NapAB in some other manner, likely to involve NapH, NapG, and/or some other protein. A few members of this protein are designated MauN and are found in methylamine utilization operons in species that appear to lack a periplasmic nitrate reductase.	3.37063e-93
NZ_CP043617.1\|WP_152306659.1\|548276_548888_+\|hypothetical-protein	gnl\|CDD\|225418	COG2863, COG2863, Cytochrome c553 [Energy production and conversion].	4.6372e-07
NZ_CP043617.1\|WP_152306658.1\|547561_548302_+\|4Fe-4S-dicluster-domain-containing-protein	gnl\|CDD\|319895	cd16373, DMSOR_beta_like, uncharacterized subfamily of DMSO Reductase beta subunit family. This family consists of the small beta iron-sulfur (FeS) subunit of the DMSO Reductase (DMSOR) family. Members of this family also contain a large, periplasmic molybdenum-containing alpha subunit and may have a small gamma subunit as well. Examples of heterodimeric members with alpha and beta subunits include arsenite oxidase, and tungsten-containing formate dehydrogenase (FDH-T) while heterotrimeric members containing alpha, beta, and gamma subunits include formate dehydrogenase-N (FDH-N), and nitrate reductase (NarGHI). The beta subunit contains four Fe4/S4 and/or Fe3/S4 clusters which transfer the electrons from the alpha subunit to a hydrophobic integral membrane protein, presumably a cytochrome containing two b-type heme groups. The reducing equivalents are then transferred to menaquinone, which finally reduces the electron-accepting enzyme system.	5.87045e-42
NZ_CP043617.1\|WP_152306663.1\|551357_552185_+\|ABC-transporter-permease-subunit	gnl\|CDD\|372253	pfam12679, ABC2_membrane_2, ABC-2 family transporter protein. This family is related to the ABC-2 membrane transporter family.	1.40608e-09
NZ_CP043617.1\|WP_152306672.1\|558115_558790_+\|response-regulator	gnl\|CDD\|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	2.57355e-41
NZ_CP043617.1\|WP_152306665.1\|552665_553190_+\|PAS-domain-containing-protein	gnl\|CDD\|369881	pfam08447, PAS_3, PAS fold. The PAS fold corresponds to the structural domain that has previously been defined as PAS and PAC motifs. The PAS fold appears in archaea, eubacteria and eukarya.	2.53517e-13
NZ_CP043617.1\|WP_152306675.1\|561062_561992_+\|cysteine-synthase-A	gnl\|CDD\|273463	TIGR01136, Cysteine_synthase, cysteine synthase. This model discriminates cysteine synthases (EC 2.5.1.47) (both CysK and CysM) from cystathionine beta-synthase, a protein found primarily in eukaryotes and carrying a C-terminal CBS domain lacking from this protein. Bacterial proteins lacking the CBS domain but otherwise showing resemblamnce to cystathionine beta-synthases and considerable phylogenetic distance from known cysteine synthases were excluded from the seed and score below the trusted cutoff. [Amino acid biosynthesis, Serine family].	3.93526e-160
NZ_CP043617.1\|WP_152306674.1\|560607_561051_+\|low-molecular-weight-phosphotyrosine-protein-phosphatase	gnl\|CDD\|319971	cd16343, LMWPTP, Low molecular weight protein tyrosine phosphatase. Low molecular weight protein tyrosine phosphatases (LMW-PTP) are a family of small soluble single-domain enzymes that are characterized by a highly conserved active site motif (V/I)CXGNXCRS and share no sequence similarity with other types of protein tyrosine phosphatases (PTPs). LMW-PTPs play important roles in many biological processes and are widely distributed in prokaryotes and eukaryotes.	3.40244e-62
NZ_CP043617.1\|WP_152306669.1\|555403_556066_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|223736	COG0664, Crp, cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases [Signal transduction mechanisms].	6.95521e-16
NZ_CP043617.1\|WP_152306667.1\|554415_554853_-\|hypothetical-protein	gnl\|CDD\|377526	pfam05573, NosL, NosL. NosL is one of the accessory proteins of the nos (nitrous oxide reductase) gene cluster. NosL is a monomeric protein of 18,540 MW that specifically and stoichiometrically binds Cu(I). The copper ion in NosL is ligated by a Cys residue, and one Met and one His are thought to serve as the other ligands. It is possible that NosL is a copper chaperone involved in metallo-centre assembly.	0.00021516
NZ_CP043617.1\|WP_152306673.1\|558776_560474_-\|nitrite/sulfite-reductase	gnl\|CDD\|223233	COG0155, CysI, Sulfite reductase, beta subunit (hemoprotein) [Inorganic ion transport and metabolism].	8.73645e-58

>NZ_CP043617.1|WP_152306665.1|552665_553190_+|PAS-domain-containing-protein
MKKPTPIDEEIELDPKRYIVSETDEKGKITFCNDYFKEISGYSEEELMGSPHNIVRHPDMPKIVFKLLWQTISAGKNINAVVKNMAKDGRYYWIFTEFEIRKDTDTGKIIGYHASRKNISKHVLAVIADLYAKLLEIEKTEGVDASEKYLINFLKDKGDDIEFANIMEEIHKFY
>NZ_CP043617.1|WP_152306664.1|552193_552664_+|hypothetical-protein
MLKIFVSLAMFIGLLNAYEMDFTKETQGLVRHIKIYKDPKWASKIELQNGKKVFFCSPKSMFEFYFRPGKWHNVGVKSEKDFKDILVTDHNTLEIIEARGAFFVYGSSVTSPAGDDLVPFNSYKEAKEFAEKYNGKRVFGFREVSDALIRLLNGRI
>NZ_CP043617.1|WP_152306663.1|551357_552185_+|ABC-transporter-permease-subunit
MKNLSLIAYLDLKESIRARWFLIYSLVFGGLIALFFIAGVTESQVMGFSGLSRLLLMYIQITIVILPIFILITTVRSISGDRDNHILEYMLSFPISLKQYYWGKVIGRFITVYLPVFFAMLIAIIYGATIGADIPWSIFFLYTGLLFSLSSAFLGIAFFVSSFVKSSEVALGIAFFVWIFMLAFLDIALISLMLSQRFNEELIIFIALANPMEIFRVAAISLFDPELTVMGPVAFYILDTMSQVVFVLLSIGYPLVLGLLFAYGGFKIFKKKDLV
>NZ_CP043617.1|WP_152308365.1|551019_551358_+|hypothetical-protein
MNVKYADDYSTEIKVKGEDFYFDDIGCMIIYAYEKNIDIEKFLPKVFTKDTKKYIPILQAKYKIGDNTPMSYGFAAYENEGDGMISYDEVVLKMLRGEHMANPKIRKKVLGQ
>NZ_CP043617.1|WP_152306662.1|550286_550925_+|ATP-binding-cassette-domain-containing-protein
MVKISNLTKKFGSHVSLDNINCEFKKNDSIALMGANGAGKTTLIRSMLGYYHPDAGEVLIDGYNPITDRTKVLENISFVPQLPPPIKLSIDELINYISTSSGVDKDLILNYANEMQLDLKSNMSKSFFKLSGGMKQKLLIAISLAKKSDIIIYDEPTANLDPKARDDFYRLLKENEQNKVLLFVTHRLEEVQELVNRQIYMDLGKVVSDERV
>NZ_CP043617.1|WP_152306661.1|549378_550284_+|NapH/MauN-family-ferredoxin-type-protein
MDKYNNRETIANSSFWSTFFDTTRDGKRIFSYRMKRWILVISIHLFFFLSFFIDLQMLEGTLNGSRFLGFHMIDIYTTMQLFLATHEMPVNMIIGTSTILIVYVLVGGRSYCSWVCPYGILSEIGEKLHNMLVKKKIIKERKFDQRVRYIFWAIFLVLSATSGYLVFETFNVVGILSRMFVYGWTVALLWVVVVFLIEVFYSRRAWCTYVCPIGTTYGFIGKVSALRIQWNDNCDSCMVCHDVCFEPQVLEITKAKYKKQIEEKNITEQYITGADCTLCGRCVDVCHEDALKFDFRLKSLV
>NZ_CP043617.1|WP_152306660.1|548889_549369_+|c-type-cytochrome
MKNTVVGILTIIIVALMGFVATDDAVYHGGEHGKVIEDMGNKTVNASSSTAPEEKDDREKEKEQLKALRDKAGNAGAFKVSQEYKSKCASCHGVNGEGIMGPKLFGQSADKVYKDLVDFKAGRKENYIMKGLLIKLEESDLRRLADEIGDFPNRAKESK
>NZ_CP043617.1|WP_152306659.1|548276_548888_+|hypothetical-protein
MNSIIKMHNLIYALIISTMIIGCSDNKQTEEKTTQVKQASASGIEVVENKDANAIKVQEKAQDKNQSKSYYFDYGIKSAYSEDAKPANSDASVRVKPRTNIDANMNVRSPYEKVQVSLLVSKLSKKFIVKCSACHNDYANGVIGPSLLHKDSEYIFSQIMKFKKDKNLNVLMSNLVENMSETEIKEIADEIYSFNKKINEMRK
>NZ_CP043617.1|WP_152306658.1|547561_548302_+|4Fe-4S-dicluster-domain-containing-protein
MATIKTDRRKFVKYSTLGVLGLAMGAGVFFSPYGKVPENRLRPPGAVEEDKFLALCIKCGQCLQVCPYHSIKLSDMAKGHGVGTPYIDASERACYACSAVPCVLACPSGALDHHCEKPEDIEMGIAYLEHPDTCLAMTNTPIPKGYNTKMHEFTKNVTNVTQLELDLLEKLDSFEGKQCTLCADMCPIPNPLSAIAMVYDSSGDGKKPEIYDGCIGCGACEEVCPTQVPSIVIKPRGTYEQYYKNA
>NZ_CP043617.1|WP_152306657.1|546347_547559_+|nitrous-oxide-reductase-family-maturation-protein-NosD
MIRLFFILLFSTLLGANILQEAIDNAPVGSILKLPAGVYKGKITIDKPLSIVGKEDGVIIDGMGEGTVIKTVGSNITLKNLTIVNSGDRHDKIDSAITMTNGKQCEISNCTIKDCLFGIDMQMVSNSIVQNNYISSKDLDLGLRGDGLRIWYSNDNIIRKNSLVKSRDMVVWYSHGNLIEENYGEHNRYSLHFMYAGKNIVKNNSYKYNSVGIFFMYSKDTVATGNVVKSSLGATGMGIGLKDVSNFTLKENTVIYCAQGIYIDRSPFEPDTNNWIENNKVLYNSEALHFHSLSENNIIKNNLIMGNIEDIVNDSRGSKTDQNDIVGNYWDNYSGFDRDGDNVGDTPHRVYQYADQLWVYDPNVKFFYGSPVISLLNFLAKLAPFTKPLFLLEDEKPKVRFEG
>NZ_CP043617.1|WP_152306667.1|554415_554853_-|hypothetical-protein
MKKLNYIITLSLLVFLGCSEKQNDGVSEVHWDRDMCARCVMVVSDRHNTVQVKDSKGKAYMFDDIGCMILWFEEEHPELKESSKIYITDVKDGSWIDAREAFYTTQNITPMAFGFSAYKSKVNIPKDEEVIDYNEVYKRVLKPKK
>NZ_CP043617.1|WP_152306668.1|554956_555394_+|hypothetical-protein
MKNLFLILSILVSITIAEETPTRTGEFPKEQMKIQAKEIAQRAAYSMNEGLPQTIDKYTELISVKAENTTMVFTFEINTGAKSDEAVRKEDHSRMQKAVTVGVCQQSQKFLESGINTSYVYTSAKTKKLLFKFDISQDKCKGLVN
>NZ_CP043617.1|WP_152306669.1|555403_556066_+|helix-turn-helix-domain-containing-protein
MSIKEIVKSLSFFSSLNDEDVEKICTISTLHKYTTGYVLHYENQDKDSIEFLVSGLAKAYKIDKHKNEIFLYHLSNDSLLSDINNISSDTLTSFSNLEMAEDSVVLKIDYTEFKQQFLNSRILCSELMNEIIKRSEYMQNIFNREFIFDAVTKVAKMIDDDLDMFNKIKRHDISLILNIQPATLSRVLSRLKRNNIISIEHGKIGIIDKEELKAIYEEVL
>NZ_CP043617.1|WP_152306670.1|556062_557028_+|hypothetical-protein
MKKIKIVIALIFLLSILLAIIFSYINEQRSVSNNFLNVINQQKAFTQEIAKNIFYMYKNQNASDKQLDDSIKKFLSNMQNRDKNLKYIDSKEIREHSKEIAVLWNKFYLEVQNFRDLNKVTVAYSNLILEELVNKIYNLNLDLVVEFNTMIDIYHKELENNISTYRNIEYILFLVLVICLIYLVSQVKDLIKFFQKFTSASKRVISNASVIGIKKIEETKTVEDVASATYAFNTLVEKIDTSILNATNSIENTYANLHTLENDIENFIELISEMHDGEEIDKELTKKEDILIESLEELNVSAENLKNLKRDFLEFANQKRD
>NZ_CP043617.1|WP_152306671.1|557029_558112_+|PAS-domain-S-box-protein
MLQQFKDAIESSNIISKTDTNGIITFVNDEFCKISGYTKDELIGQNHNIVRHPDVDKNNFKELWNTIKNKKIYKSTVKNLAKDGSVFYVNTTIIPILDDNDDIFEYIAIRYDVTKEMFYKEELEKNEVKQKILFAQARHASLGQMLANIAHQWRQPLTELSLTVFNLKKNALSKDEEALQKYYEESKNIINSMSKTIEDFSNFFTPNREVEQFDIKLSVDEALELMDNSLKSSMVDVEFRIQNDLEVLGVANELTQVVLNLLKNSIDAFELNGVLIRQIDITIRRLKDSAEIEFRDNAGGIKKDIVDRIFEPYFTSKHQKNGTGLGLFMSKMIVEQSFDGSLDVKSKKHYTIFSIKIPTA
>NZ_CP043617.1|WP_152306672.1|558115_558790_+|response-regulator
MRDKKLKTLKVLLVEDEQAIAELLKSAIGDNFRSFIIANDGLEGYELYSKITPDIIITDIMMPNSSGLELAKKIRLNDRLIPIIILSAFSEKEKLFGAIDAGVTKYFTKPYDPDEILEYIHTIASEIQEKTLELCDDFSFDKNNHSLYKESSFVKLSKNETSFITLLAESLERRLSYEDIKSSMWEDKDVSDERLRTFVKRLREKTSKNLIETIKGYGYRLNES
>NZ_CP043617.1|WP_152306673.1|558776_560474_-|nitrite/sulfite-reductase
MVDEKLNKREKYKARLRPIDYYKDFENLDFENLGEGDRFYLQDFGIFTTDFLEDEFTIRIRLAGGRIGTKEFQAIADIVKEYDLTIVMTARGGIQLHDIYVDDVLEIHKRINSLNLTTWQSFGDNIRNIVTDAYDGVIAESEIECYPIIEQMQDFILQNPRYVGMLPRRVSIGISGNSVNVNSFFANDIYFALAKKDGVFGFNVYMGGKNTDVAQDVDIFLHKEDVFDFFKAFVETFYTHGSRYSRSRTRLIYLIEDIGIDKLKELIQNEYKKEFLTSGELVLNKGKFSEYRELKDGTYAFVYQTNFSKLTADEMNKIAEFATKNDAQIRLGIDQNIYILGLKEKKSPLISPSNSSTVVACAGNLCPYAVWSIKEETKYLPLDLIQKHSIFVGFSGCAKGCGRHRHTDIGLIGLKTNNFGDTDGGCRIFIGAEHSDGKSVGRELFSMVPFVHLNSVVTLIISLFEKSGYSDFETYSKEILNNYSELFLSLWHLANLESKQTIALPKQSKKISQEDEEKLLKDNFKELEIHEDGFRKTISLKVKELWTIEGKDPNYKPPIERTNFR
>NZ_CP043617.1|WP_152306674.1|560607_561051_+|low-molecular-weight-phosphotyrosine-protein-phosphatase
MKSIIFVCLGNICRSPLADGIAKKYIKDNALDISVDSAGTGNWHVGENPCPNSIKVAKNNGIDISALVSRQVTKNDFEIYDLVVALDDNNMNDLTALGAKNIVKLGDYGFYGKDVPDPYFYNGFEGFDKVYDMIQKCVINLIDEYTK
>NZ_CP043617.1|WP_152306675.1|561062_561992_+|cysteine-synthase-A
MANIANDVTELIGNTPLVRLNKASQITGATILGKCEFMNPTSSVKDRLGFNMIRRAQEKGLINENSTIIEPTSGNTGIALAANCAAQNLKLVLTMPESMSIERRNLLKALGAELVLTSAAKGMSGAIEKAKELEALTNNSIILQQFENDANAEIHELTTAREILRDTDSNIDAFVAAVGTGGTLTGTARVLKKEIQNIAVFAVEPKDSPVLSGGNGGPHKIQGIGAGFIPKVLDTSVYGEVVQVSNEDAIETAKMLAREEGLLVGISAGANVWATMQVAKRDEFKGKILVTVLCDTGERYLSTALFNEE
>NZ_CP043617.1|WP_152306676.1|561981_562578_+|branched-chain-amino-acid-aminotransferase
MKNEFLETIKILDAKVWHPEYHQKRYESVLKHFGVCTYKKLEDFIKPPKKGLYRCRLVYTPEDIKKISVEYIEYEKKDINTLKLVYDDEIDYPLKSTDRSELNKLYEKRQDADDILIVKKGYLTDTSIANIALFDGEWKTPKYPLLKGTTRQRLLDSGKIHEDDIKVQDIGRFSKVALLNAMIDFDIIADENIKDVFC

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP043617_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP043617_3

819344-819949

Orphan

Consensus_repeat	Method
ACAACGGATGAAGCTACGGTAGATGAAGTTCCTGAAAGTACTGTAGATGAA	CRISPRCasFinder

4 spacers

The CRISPR arrays of NZ_CP043617_3

>merge|NZ_CP043617|3|819344-819949|CRISPRCasFinder
ACAACGGATGAGAGTACGGTAGATGCAGTAGCAGAAGATACAAGTGATGTAATAAATACGGAAGCACAAGCTGAACAGACCGTAGATGAAGACACTGTAGATGCGGTAGCGGAAGATACTACTGATGAAGCTACTACCGATGCGGTAAATGAACAAACAACGGATGAAGCTACGGTAGATGAAGTTCCTGAAAGTACTGTAGATGAAAATACTATAGATGCAGTAGCAGAAGATACAACGGATGAAGCTACGGTAGATGAAGTTCCTGAAAGTACTGTTGATGAAGATACGACAGATGCTATCCCGGAAAGTACGGTTGATGAGAATGTTATAACAGAAGCTAGACCTGAGGCAACAGTTCTTTCATATGAAATAATAAGCCAAAGACCTGAAGATACGGAACCTGAGAGTACAATAGATGCAGTAGCGGAAGAGACTACGGATGAAGATACTGTAGATGCAGTACCTGAATCTACAACTGATGAAGTTGTTAATACTCCGGCAAGTGATGAAGCAACTACTGATGAAGATACTACGGATGCTACACCGGAAAATACTGTTGATGAAGCAACTGTAGATGCCGTACCTGAAAGTACGGTAGATGAA

>NZ_CP043617|3|3|819344-819949|CRISPRCasFinder
ACAACGGATGAGAGTACGGTAGATGCAGTAGCAGAAGATACAAGTGATGTA	ATAAATACGGAAGCACAAGCTGAACAGACCGTAGATGAAGACACTGTAGATGCGGTAGCGGAAGATACTACTGATGAAGCTACTACCGATGCGGTAAATGAACAA
ACAACGGATGAAGCTACGGTAGATGAAGTTCCTGAAAGTACTGTAGATGAA	AATACTATAGATGCAGTAGCAGAAGATACAACGGATGAAGCTACGGTAGATGAAGTTCCTGAAAGT
ACTGTTGATGAAGATACGACAGATGCTATCCCGGAAAGTACGGTTGATGAG	AATGTTATAACAGAAGCTAGACCTGAGGCAACAGTTCTTTCATATGAAATAATAAGCCAAAGACCTGAAGATACGGAACCTGAGAGTACAATAGATGCAGTAGCGGAAGAG
ACTACGGATGAAGATACTGTAGATGCAGTACCTGAATCTACAACTGATGAA	GTTGTTAATACTCCGGCAAGTGATGAAGCAACTACTGATGAAGATACTACGGATGCTACACCGGAAAAT
ACTGTTGATGAAGCAACTGTAGATGCCGTACCTGAAAGTACGGTAGATGAA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP043617.1\|WP_152306903.1\|836329_836758_+\|DUF255-domain-containing-protein	unknown	unknown	gnl\|CDD\|379399
NZ_CP043617.1\|WP_152306892.1\|815273_816383_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP043617.1\|WP_152306890.1\|812675_814913_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|370774
NZ_CP043617.1\|WP_152306888.1\|808605_811530_+\|type-VI-secretion-system-tip-protein-VgrG	unknown	unknown	gnl\|CDD\|274542
NZ_CP043617.1\|WP_152306902.1\|835230_836328_+\|succinyl-diaminopimelate-desuccinylase	unknown	unknown	gnl\|CDD\|237265
NZ_CP043617.1\|WP_152306891.1\|814915_815224_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP043617.1\|WP_152306885.1\|806351_807032_+\|SpoIIE-family-protein-phosphatase	unknown	unknown	gnl\|CDD\|223704
NZ_CP043617.1\|WP_152306886.1\|807019_807886_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP043617.1\|WP_152306887.1\|807991_808516_+\|type-VI-secretion-system-tube-protein-Hcp	unknown	unknown	gnl\|CDD\|213799
NZ_CP043617.1\|WP_152306896.1\|823600_824206_-\|DNA-binding-response-regulator	unknown	unknown	gnl\|CDD\|225107
NZ_CP043617.1\|WP_152306904.1\|836754_837132_+\|deaminase	unknown	unknown	gnl\|CDD\|129116
NZ_CP043617.1\|WP_152306900.1\|829606_830383_-\|OmpA-family-protein	unknown	unknown	gnl\|CDD\|143586
NZ_CP043617.1\|WP_152306897.1\|824210_825551_-\|HlyD-family-type-I-secretion-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|130902
NZ_CP043617.1\|WP_152306894.1\|816914_818033_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP043617.1\|WP_152308379.1\|833602_834424_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP043617.1\|WP_152306898.1\|825534_827709_-\|type-I-secretion-system-permease/ATPase	unknown	unknown	gnl\|CDD\|274550
NZ_CP043617.1\|WP_152306889.1\|811516_812686_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276807
NZ_CP043617.1\|WP_152306899.1\|827727_829590_-\|TolC-family-outer-membrane-protein	unknown	unknown	gnl\|CDD\|273829
NZ_CP043617.1\|WP_152306901.1\|830576_833606_+\|DNA-mismatch-repair-protein	unknown	unknown	gnl\|CDD\|223327
NZ_CP043617.1\|WP_152306893.1\|816390_816855_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379331

Protein	Function_ID	Function_description	E-value
NZ_CP043617.1\|WP_152306903.1\|836329_836758_+\|DUF255-domain-containing-protein	gnl\|CDD\|379399	pfam13899, Thioredoxin_7, Thioredoxin-like. Thioredoxins are small enzymes that participate in redox reactions, via the reversible oxidation of an active centre disulfide bond.	1.82243e-06
NZ_CP043617.1\|WP_152306890.1\|812675_814913_+\|hypothetical-protein	gnl\|CDD\|370774	pfam09994, DUF2235, Uncharacterized alpha/beta hydrolase domain (DUF2235). This domain, found in various hypothetical bacterial proteins, has no known function.	9.84286e-13
NZ_CP043617.1\|WP_152306888.1\|808605_811530_+\|type-VI-secretion-system-tip-protein-VgrG	gnl\|CDD\|274542	TIGR03361, VI_Rhs_Vgr, type VI secretion system Vgr family protein. Members of this protein family belong to the Rhs element Vgr protein family (see TIGR01646), but furthermore all are found in genomes with type VI secretion loci. However, members of this protein family, although recognizably correlated to type VI secretion according the partial phylogenetic profiling algorithm, are often found far the type VI secretion locus.	1.51402e-96
NZ_CP043617.1\|WP_152306902.1\|835230_836328_+\|succinyl-diaminopimelate-desuccinylase	gnl\|CDD\|237265	PRK13009, PRK13009, succinyl-diaminopimelate desuccinylase; Reviewed.	0
NZ_CP043617.1\|WP_152306901.1\|830576_833606_+\|DNA-mismatch-repair-protein	gnl\|CDD\|223327	COG0249, MutS, Mismatch repair ATPase (MutS family) [DNA replication, recombination, and repair].	5.32251e-99
NZ_CP043617.1\|WP_152306899.1\|827727_829590_-\|TolC-family-outer-membrane-protein	gnl\|CDD\|273829	TIGR01844, Proteases_secretion_protein_PrtF, type I secretion outer membrane protein, TolC family. Members of this model are outer membrane proteins from the TolC subfamily within the RND (Resistance-Nodulation-cell Division) efflux systems. These proteins, unlike the NodT subfamily, appear not to be lipoproteins. All are believed to participate in type I protein secretion, an ABC transporter system for protein secretion without cleavage of a signal sequence, although they may, like TolC, participate also in the efflux of smaller molecules as well. This family includes the well-documented examples TolC (E. coli), PrtF (Erwinia), and AprF (Pseudomonas aeruginosa). [Protein fate, Protein and peptide secretion and trafficking, Transport and binding proteins, Porins].	1.11407e-60
NZ_CP043617.1\|WP_152306886.1\|807019_807886_+\|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.	2.31969e-49
NZ_CP043617.1\|WP_152306887.1\|807991_808516_+\|type-VI-secretion-system-tube-protein-Hcp	gnl\|CDD\|213799	TIGR03344, VI_effect_Hcp1, type VI secretion system effector, Hcp1 family. This family includes Hcp1 (hemolysin coregulated protein 1), an exported, homohexameric ring-forming virulence protein from Pseudomonas aeruginosa. Hcp1 lacks a conventional signal sequence and is instead exported by means of the type VI secretion system, encoded by a pathogenicity cluster of a class previously designated IAHP (IcmF-associated homologous protein). Homologs of Hcp1, in this protein family, are found in various bacteria of which most but not all are known pathogens. Pathogens may have many multiple members of this family, with three to ten in Erwinia carotovora, Yersinia pestis, uropathogenic Escherichia coli, and the insect pathogen Photorhabdus luminescens. [Cellular processes, Pathogenesis].	9.97906e-75
NZ_CP043617.1\|WP_152306896.1\|823600_824206_-\|DNA-binding-response-regulator	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	2.76987e-19
NZ_CP043617.1\|WP_152306904.1\|836754_837132_+\|deaminase	gnl\|CDD\|129116	TIGR00004, RutC_family_protein, reactive intermediate/imine deaminase. This protein was described initially as an inhibitor of protein synthesis intiation, then as an endoribonuclease active on single-stranded mRNA, endoribonuclease L-PSP. Members of this family, conserved in all domains of life and often with several members per bacterial genome, appear to catalyze a reaction that minimizes toxic by-products from reactions catalyzed by pyridoxal phosphate-dependent enzymes. [Cellular processes, Other].	2.53789e-53
NZ_CP043617.1\|WP_152306900.1\|829606_830383_-\|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.	1.37706e-39
NZ_CP043617.1\|WP_152306897.1\|824210_825551_-\|HlyD-family-type-I-secretion-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].	6.55911e-110
NZ_CP043617.1\|WP_152308379.1\|833602_834424_-\|hypothetical-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	3.55384e-34
NZ_CP043617.1\|WP_152306898.1\|825534_827709_-\|type-I-secretion-system-permease/ATPase	gnl\|CDD\|274550	TIGR03375, type_I_sec_LssB, type I secretion system ATPase, LssB family. Type I protein secretion is a system in some Gram-negative bacteria to export proteins (often proteases) across both inner and outer membranes to the extracellular medium. This is one of three proteins of the type I secretion apparatus. Targeted proteins are not cleaved at the N-terminus, but rather carry signals located toward the extreme C-terminus to direct type I secretion. This model is related to models TIGR01842 and TIGR01846, and to bacteriocin ABC transporters that cleave their substrates during export. [Protein fate, Protein and peptide secretion and trafficking, Cellular processes, Pathogenesis].	0
NZ_CP043617.1\|WP_152306889.1\|811516_812686_+\|tetratricopeptide-repeat-protein	gnl\|CDD\|276807	sd00010, SLR, Sel1-like repeat. Sel1-like repeats (SLRs) share similar alpha-helical conformations with Tetratricopeptide repeats (TPRs), but with different consensus sequence lengths and superhelical topologies. SLRs contain 36 to 44 amino acids and are present in bacteria and eukaryotes but not in archaea. SLR proteins are involved in a variety of functions, and many serve as adaptor proteins for the assembly of macromolecular complexes. The SLR family was named after the Caenorhabditis elegans Sel1 protein which is predicted to fold into 11 SLRs, a transmembrane domain, and an N-terminal signal sequence. The human Sel1L protein contains an additional fibronectin type-II domain and an N-terminal PEST sequence. Its downregulation is associated with the development of breast and pancreatic carcinomas.	1.03762e-14
NZ_CP043617.1\|WP_152306885.1\|806351_807032_+\|SpoIIE-family-protein-phosphatase	gnl\|CDD\|223704	COG0631, PTC1, Serine/threonine protein phosphatase [Signal transduction mechanisms].	2.93114e-39
NZ_CP043617.1\|WP_152306893.1\|816390_816855_-\|hypothetical-protein	gnl\|CDD\|379331	pfam13682, CZB, Chemoreceptor zinc-binding domain. The chemoreceptor zinc-binding domain (CZB) is found in bacterial signal transduction proteins - most frequently receptors involved in chemotaxis and motility, but also in c-di-GMP signalling and nitrate/nitrite-sensing. Originally discovered in the cytoplasmic chemoreceptor TlpD from Helicobacter pylori, it is often found C-terminal to the MCPsignal domain in cytoplasmic chemoreceptor proteins. The CZB domain contains a core sequence motif, Hxx[WFYL]x21-28Cx[LFMVI]Gx[WFLVI]x18-27HxxxH. The highly-conserved H-C-H-H residues of this motif are believed to coordinate zinc; mutating the latter two histidines of the motif to alanines abolishes Zn binding. This domain binds zinc with high affinity, with a Kd in the femtomolar range. This domain has been shown in E. coli to be a zinc sensor that regulates the catalytic activity of pfam00990.	3.58816e-06

>NZ_CP043617.1|WP_152306894.1|816914_818033_-|hypothetical-protein
MKIKEAIISLDIMPRETYDKFSKFSKLQNASPDEIWKHYPSTGLNNYNPQTMVLEASIIETYLLLDYLKQNKIKARLWYNNPLFIHNEKLFRIKGDEVVEENIENLYFVSLREALAHPFFRILKIILEAKGGALVKPNMQTMQNTGCMNKFYAKRELYSKREKYLGDVIIPFNITQRDHKTFMKYVRENLGDKIVLKKDCVQEGKGVIFKDLSRDNQMQSISKILNSHKSKDREVLISKAYDIEREYRCYFTKHGDKKTVYSIKQRVNHEDIDVFDKDDITIYKNISVKWHEVKTDSDVFKFGSELTYEMLELMTFDTGCLEFAQTTTGEIVFFEVNQMAGPLPFAGEDTKNMTRYYHSIFDNMFKTKEKSD
>NZ_CP043617.1|WP_152306893.1|816390_816855_-|hypothetical-protein
MDKQQTLEHLRAAKASHLEWTQHAKFLIRGMNIEEKAIPVNSMDCNFGKWFYKEGQKLNGLPNNPAECMSEIEQLHFQLHDVYFNIYNIYYTKQKKGFLSKIFGDKREVSAQDVKMAEKYFEELEVISKKLIEELNRLERRLLAVPDKKIEELF
>NZ_CP043617.1|WP_152306892.1|815273_816383_+|hypothetical-protein
MSINGRILFYNSQTGEGKLILDTKEKIDFSVDVWDDFEVGPQSNILVECDIEDGILKSIKASPLDEPMQKSNFQKQETQKMFFDEDGGARYSVSETLKNYFSHIEDVIGEPPEIINTKAQLDYFLSKRFLLTAYNNLRGLDPSLYERKNIKEKINTIEELHKAYNSITEKIDIPHLAFEMIFLRVQPEYIEYQKKKEKYLNNIPILTKLINSLEPELKKGEGNLKVIKNPKISTELKNKLKKIRGRYVDAIHERACITEELSEMPDIKAIYTDRYFHDFERELSILQVKYKDMISRILNYKAYDLDVSIWQNASKSKMIQEYFKDAGIKGGYSTKTFLRYYLETLDKDKVKEEQEELFKLLDYLEKITK
>NZ_CP043617.1|WP_152306891.1|814915_815224_+|hypothetical-protein
MYELKEIIYYLRKFDLDEKSIKKCYEMIPDPAGKVESQDKLFIECQTQYHINTIGSFIENITRGIEKGYITEAIKKTAREFSYVREIPRIAFYVVVLSKVVK
>NZ_CP043617.1|WP_152306890.1|812675_814913_+|hypothetical-protein
MMSKPFSIGTVVYNGSEFMSVAKVLSNEEVSSTSHDMCVPRDEYNHWAYLIVGYEESKSLRTGVKEDKKILENIKNKYIQILKSAIESTEGKIQSNGYEIDNKLVYHQISGVKSTKNLKHFLQSEKFTCQAKKLKDSENSILQSRMYLKLTNQEANQLLQKEYDTLNPDQKKKVHAYAFVAMPYTYSNDKLKLNSEAVFVAFMPRVQFEAGVFFDGTLNNMYNTNLRVDFEKYTQAQVDVLGGFSSQEKISTNGPKRFLEGAPKEEVLEKIQTDLKKSINFYKNGIGDSKLKDYVEKSAKGASEELYAYFEDVLSRKASSVEEFVKEELLPDKGSYQNDQSNIAILHSLYDTNIKDSKSKGEFFRKSIYITGAGSYNPYLKKEHESDALLGKALGMGETGVLAKVNQACKFIKESIEQKNLSYIDTLVFDVFGFSRGAAEARHFVNSIADELDLKLKNDNKEFVLYKKDGSNLYPYLIKEIEGKKDEVIIDKIVFRFVGIFDTVSHYGLYQEDDKEDELNLVFDDTKISNVLHLVAKDEYRENFALTKLQTNVRHFEEKSFHGAHSDIGGGYIDGKDEKIQLYKSYNIRENSLVKTKKSLESKLKKWNKKYRWLQNDLISYKYDVKDGFYIQITKRIRGSHRNVSYTLSAWMIRSSVSSEYSKIPLEYMHKKLKELKIPFTSLGTHKVTDSILKQNQQKIVNLDENTIKSIRAKYFHHSSDLSGVGMDGADAIDDSEFYGKRVVY
>NZ_CP043617.1|WP_152306889.1|811516_812686_+|tetratricopeptide-repeat-protein
MMKYKLSILLLLVSILNAEIKECFLVENKTEFIGCLESEVKKSDSVKDTNFLASIYVNDKEYEKAIKLYEKSVEKGDVKAMYYLGGIYNEALKDYDKALYWFERSYEYNYKDSSAFVAEILSKKFNNNQEAVKNYLQKRIDANDSKAYEFLGAYEYNLKNYKKAIDYYKKAVKAYNSPQAMYAIGSIYYQHLKDTNKGMKWLKKASKLQHPDGVYSVGFIYKDKKEYKKAIEWFNKALDLGVKGSHYAISECYRKMGEFDKAKEQYLKMVKEGNIKGYREIGVMYSLYPEIKDEIKEMKWYERGIEARDGSAAAAAAVGFRDKKDYENFLKYNKIAYSLGYAGGANEIAYYYLRTVKDEKKAIEWGKRANRLGDPMFLKFLKNIGVYDE
>NZ_CP043617.1|WP_152306888.1|808605_811530_+|type-VI-secretion-system-tip-protein-VgrG
MAVSTLPTVNNSSKITKQLTNKINQRIVTDIVLKTLSNESFSVYRLSGSSEVGETYEFNVSFVSSHAIDIEDIVDTDVKISIKDENSLQIKEIYAKVYKASEDSVVASKYMYKLHVVSPLYYLKFNKRYEIYHDKKASDIITEIFNRYGSVLNIRLENKIDSEKIPLREYTTQYNQSDLEFIEMLCKEEGYSLVYHYSSEDKDFFTSAFEFTLCELNEHCKVINHSAVADFNISKKFVPTNVLEDYYDYDKPSLDMKTEFGATLDTEFLKDNSSTKQLRSHLQTHTLRDKLNVQDESLYKDLKRYSQIDAYANMAQSRVIEANTQELFIHDSMAIELHDEKAGKNFEVIITKCEYKIVSPNALEEYIEAEEFSDELEYEVHFEAIPKDVIYKPLQTTHKPKINSIQTAIVSKGTQQSDESANEIDVDEKGRIRVLFHFEQNKETSCYIRVASFYNGDGYGAQFLPRVNSEVLVSFINGDIDKPVVVGSLYNGENKLPYNLPKDKTKSYIRTHSIPAYEEEFGYNEISFEDKRGEEKLYQRAQKDYELEIKNNYKAVIDHDMHSIVGNDETQSINNNYKQTVGNDSTRQIQANDIKVVEKEEVHTINEDKELFVLKDYNTVVEQSKKTIVEKDMIHRVKGILHQYVHKDVKHKLLSNLFIQVGKDYRLDVTQSYHVKSKSEKHTTGTFEILAQDGISLKCGGSVLTVDGSGIHLKAPNVDTASGNGGVEATAVEKVEIEKPVYNKVRVTSLSVDVEKQVDITDILTFTAEVEVYEDDAWVAKTELTDTQKSQVVWAFVKNNDENDKDILTDNPVNDNITEDGLTMTVNVDEENIYKYAHVHCYVADSENEGYAMSELKRYLEVENILPNGGLDENSKVDCQAILNVEDPRADELEQIRWSINDKDKAEFNGKETITHDMNNESTRSVMFNAYIDGSKELMASCELQNTKKVQESSNTTSNEKSSSKNRDIEHDEI
>NZ_CP043617.1|WP_152306887.1|807991_808516_+|type-VI-secretion-system-tube-protein-Hcp
MNNPIFISIEGSTQGLMTEGAFTPESVGNSYQEGHENEALVKEFKHTIKVPRDPQSGQPSGQRIHEPLIVSKLFDKSSPLLYNALTKGETLKNVEMKWYRTSYEGKPEHYFTMVLEDAVIVNISSDMGLEDNKTTSQIAPMEKVSFAYRKITWRHEIASTSGEDDWRLGVSKMA
>NZ_CP043617.1|WP_152306886.1|807019_807886_+|protein-kinase
MCIIGSNKNKQALIEDIYENTSGIFNQRYIIVEYISFGGMSVVFKVKDIYCEYFNENKQLVIKIPIKNLLKKDDIAAFMYSEYTFLRDLNNENIVKVYDYGIDINTDIPYIVMEYLDGSLLENINLQNLKYKDKIFIFKNLHNTIRHIHKKGIIHADITPKNITVVHNKFITLFDFGISKRINTEKKMELDYNQAKAYNPKYSAPEIINGGKPTVESDLFSLALVLYEIFTTNLPFNINSLELEKKPLTFLNCPKQIPFILKIWFVKNLNINPKKRTNKLSILHKVII
>NZ_CP043617.1|WP_152306885.1|806351_807032_+|SpoIIE-family-protein-phosphatase
MKNKSFSFTHPGHKRRVNEDSFYVNDEKGLWVVCDGMGGHEEGLFASSLATDSFSALELNSTFNDNVERILQTIHFIKQQLDKKVYTLDINDFVGTTLILLYIKDGKALCISAGDSRCYILRNDKLSLVNKDHTRDVIDAKQETRSVLTNAIFAPGDINIDIKKFTINKNDVFLLCSDGLYSYLNIKEIKHAMNLAFEGRGLNLLKTSVLSQDADDNLTGAMICVL
>NZ_CP043617.1|WP_152306896.1|823600_824206_-|DNA-binding-response-regulator
MQIIFFSSDENTINEWRNKYNTQDFKSCYDIESLNNEIKNIEKFILVCDYDSIAHDLNTLISSKTLPYYSVVLERSPAIATGKILIKNGVKAYGNSKMLLKHFNQLVDTVKENKTWTYPELTAALVKSTKKTSINSDAAELIESRLTLKERDVVLLVLEGLTNDAIANELGITTRTVKAHISSIFSKLHVNDRISLVLLLK
>NZ_CP043617.1|WP_152306897.1|824210_825551_-|HlyD-family-type-I-secretion-periplasmic-adaptor-subunit
MSKNNKPVEYTDKDYEFMQSLSSAILEHTPTRVSAIIKIWLITIVVFIIWASLAKIDEITRGDGDVVPYGQNQIIQNLEGGIVESIFVHEGQTIKKGDKILKINNAESLSKSETNKMKYEELLAKKYRLEAEANQEEFKSELTDNPELNRQIALAKNLYESNKIEFEAKDNVIVQQIEQKKQEYKEAKAKLKSLNVSLEYVSQEIAMTAPMVREGVKSKVDFLKLKREANGIENDIEAAKLSLPRIESTIKEFRQKRIENKQLFINTAKKELNEVTAEILRLQTQQVAYSDEVKRTVVTSPVDGIVQKLYVNTIGGVIKPGADLVEIVPTNEKLYLEVKIKPSDIAFLHPGAKAKVKVSAYDFAIHGGLVGKIVNISPDTITDKEENTFYLINIETEKNYLGTKEHPLKIIPGMTVSVDIVTGKKTIMQYILKPILKSKQYVFSER
>NZ_CP043617.1|WP_152306898.1|825534_827709_-|type-I-secretion-system-permease/ATPase
MLIAEADNLRMDSLLDCLVLFTKLYHKPFSAEALSAGLPTEPGHETPELFSINNAKGLFSRAAERAGLKSSLIRRPLSHISTLQLPMIILLSNQSACILERFSEDRTQAKIIMPTDEAVEQWVDLDVLEDEYIGFGFMIKKAYEYTDDNTRTLHLNQKHWFWSTIKLSLPIYKDVIYASLLINIFVLASPLFTMNVYDRVVPNNAIETLWVFAIGVAIIYGIDTFLKFTRTFLLETAAKKSDIIMSSIIFEKVLDLKMAHHPASVGSFSSNLKDFDSIRSFLTNATMAAIIDLPFAVIFLAVIGYIGGSIVFIPMVTMFLILAYAFFIKNPLRKSIESTHEANAKKNSILIETLNNIETLKTLGTINQVQYKWEESTGEIAGKSLKSRLLSASIPTVTQLLIQLNTVMIIIYGVYLIQDFELSMGGLIAIVILTSRTLAPMGQVAALMTNYEDTKTSYETLNDIISKPTERPSGKKFVERPKFSGHIEFVDVTFTYPNTEIPALKNVSFIINPGENIAIIGRIGSGKSTIQKLLLGLYEPDSGQILIDGIDIKQIDPADLRKNIGYVSQDIMLFRGTVKDNITFRASHASDVAMIKAAEVSGTSEFIKKHPKGYEMPVGERGQGLSGGQRQSIGIARAFLLDAPIMLMDEPTNAMDQITESKLLDNLETNLKDKTSIIVTQKMTILKIVERVIVLNEGKVFIDAPKEEALLKLQGGGNKVEQKQ
>NZ_CP043617.1|WP_152306899.1|827727_829590_-|TolC-family-outer-membrane-protein
MNKKLIFLPLSLVTLLSAQDLRTTVEEVINTNPTVQERLKNYNATKEDIKIAESEYYPTLDLSIGVGVENNQKKTDYSGASTLIEKGGPNITNSNTLSVYQNSLTFTQNVFNGFSTTNKISQQQHRTTSAAYSYIENVNDISFKMVDAYLQVMRNKELLETAQANVDINEEIFKKVQKLYDAGLTTLSEVNKIESSLSLAKSNYVVQENTLLDVTYNMQRVFGRYLDVDKMQKPVLNVALPGSIEEAAQYSIQNNPSLLVAAYNVKLAQAGYKQQKSAYYPTIDIEISQNMNKNLSGIQGKDERLRAMAYLRYNLFNGFSDEARVQQSVSKIHQEVENKNDLRRQVLEGLNLSWAANEKLGDQLEHLNEYKKFSFKTLTLYAKEYDLGRRSLLDLLSAQNDFIGAKQQIINTQYSMLFAKYRILDAMGTLVQTVLGNTDIVYSNVGLNGKTPQNMDSLPISYDKDLDLIVDEYDLCSNSLNDKMRNIYGCKFVFEDTLKIERYTGFYTNDTDDNNATALNEEGTLKLNGLVQQISPYGFEYLKFDILGNVDDAKMSDLDKIELSKQRAIYVKDQLVKAGAKEENIKIHANSDKAPMFSRELDEAIEKNNRVDIVVKKLYK
>NZ_CP043617.1|WP_152306900.1|829606_830383_-|OmpA-family-protein
MKIKVNFLIIAFLSVSLYAQNIIKENNQSISEYQFVKPIAIEKAPVKEIVPQETVSDKDGDGVLDEKDRCPNTKEGEKVDEFGCLVKLDSDKDGVPDSDDKCPNSQEGTQVDYRGCEVDSDGDGIADSKDTCPDTSKEFVVDGYGCPQTATLNVNFKSSKWDIDEKLISDLQTFALFLKENKGYDVIIYGYTDSVGKAAANKTLSQNRAEAVKEVLTRYGISTTRLTAIGKGEENPIGDNSTKEGRAQNRRIEVELLQ
>NZ_CP043617.1|WP_152306901.1|830576_833606_+|DNA-mismatch-repair-protein
MKHSEVDKILNNKKNLLTQTYFELQEHFENKYGYDTVVFMEIGTFFEVYEVNNDDMQIGKAKEIAELLNIQLTKKNKNIIENSDKNPLLAGVPAVSFERYLSRLISEQKYTIIVVKQKGNPPKISRYISQIVSPGTNFDYIVDNDDNYIVSLLVDKHKDIYTVGYSAIDVTTGKTWLYETHGTSEDPSYALDEVFNLLNVYRTSEVVITFLDGIDDQRHVMQYLEISEHYHYSVNNDRPKIDFQNELFKGVYQIQSLLSPIEHLDLERSPMITEALAILINFVVEHDYHIVQKLSMPKTIDNRRFMYLGNNALEQMGVISKDKKEFTLLKMMDKSSTAIGRRLLKERLLNPIMEKDELERRYNLVERVNSHVRFLDETMRGIYDLERLSRRLNLSKLHPFEMNHIYDSIVSVKELMQYVKKHKIQKTPFSEFEIDEFLRDIQKSIDLDVSRRFTNQTVDENFLMSGVDEAIDTLVKENSVMLIAFDDIMAKIESMLKDANASSSNKLVTLGLLEKEGYYISLSKTRFSMIESEFKKSEEFSEFIVKKLTNNVKITSAFTDNLSDKIMQNRRKIITLVKERYIQLQSLYERRYALLFDRIISYVADLDVGVSSSKVAQTYNHSRPMIVDVADEDNFMQLMQLRHPLIEVQERGGIYVPNDIVMGNRDYMDLPHPKTVMLDVSVHDGHDVNGVLLYGINSSGKSSLMKSIGIATLMAQSGFFVSASVMKFSLFDSLFTRIVSRDNLAKGLSTFAVEMLEMKNIFNRATLRSLVLGDEISHGTETLSGVSIVASAIMKLAKVRSLFLFATHLHQLSTMKEITSLDNVVDLHLSVEYDEDKDALVFNRVLQAGSGSSIYGLEFAKSLHMDEEFLDTANKIRKRLAKDFDELELLVKKKTSKYNKDLYVTKCVICGAMAEDVHHINNQSLANQAGFIDHFHKDAKHNLIPLCKEHHKEIHEGKLRVDGFVMTSNGLALKYEQQMSKPKEKVVEEPEINETNEDEPKGFVLDDWD
>NZ_CP043617.1|WP_152308379.1|833602_834424_-|hypothetical-protein
MFVNLAEYVKQLKSFNNELEKRVKDEINKQQNQEHMMIHQSRQAAMGEMLESIAHQWRQPLNIIGIATANLETEYDLGLINEKKFHEKMDVISLNLNYMSDTIDDFRDFLNPKKDMSIFEAEKSIEDVLTILSAQLQNYNIEYSLQCNDELLLYGVENEFKQVMLILLNNSKDAIKLQQKIEQSKKGKILISINRENNQGIIKLCDNGGGIASEIIDSIFEPYFSTKLNANGTGIGLYIAKNIIESRMNGKISVINKDSGCCFIISVPLSIGN
>NZ_CP043617.1|WP_152306902.1|835230_836328_+|succinyl-diaminopimelate-desuccinylase
MQIIELFKRLIESKSETPDDGGLLDFIENYLDGFSAKRIDIEDTKNLFIYKKFSEGEHLCFAGHVDVVPAGEGWDTNPYELVEKDGYLYGRGTQDMKSGVAAFVQAVSEVKDFNGTLSILLTSDEEGEATYGTIKVLEYLKETSFLPDAVVVAEPTCEKKFGDAIKVGRRGSINGYITLKGKQGHAAYPEKAINPIHNIAGVLGNMAGINIDEGDEFFSPSKFVVTDIRSGMQVTNVTPNELKMMFNVRNTTLTTQKEVREFVHQNLKEFDYELKLTQGSYPFRTNTDTKLVKNIDLAIEETTGLKPKHSTAGGTSDARFVAGFGIDVIEFGVKNDTIHAVNERTTAYEVESLYKVFKRLIQIWE
>NZ_CP043617.1|WP_152306903.1|836329_836758_+|DUF255-domain-containing-protein
MRKIFILLLLVNLLFSEEIGELTFSNDYKKVMAQAKKENKRVYMLITSSSCRWCRKFESTTLTDWTVAEKLEGKYLLLHIDRDNDYFPKHLKHKRVPRHYFLTPDEQVIYTFLGYWNVEDFTSYVDDVDWQYSDKLKKGIIK
>NZ_CP043617.1|WP_152306904.1|836754_837132_+|deaminase
MKFVQTDKAPSAIGPYSQAVVVEGMVYTSGQIALLPDGCEDVLKDGIAPQAKQVMANLKAVLEEAGSSMDKVVKTTIFLASMDDFILVNGIYEEAFGSHKPVRSTVAVKTLPKNALVEIDAVALI

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Crispr_ID: NZ_CP043617_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP043617_4

2137265-2139407

TypeII

Consensus_repeat	Method
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACCAAA	PILER-CR
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CRISPRCasFinder
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CRT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	PILER-CR
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	PILER-CR
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	PILER-CR

32 spacers

cas2,cas1,cas9

The CRISPR arrays of NZ_CP043617_4

>merge|NZ_CP043617|4|2137265-2139407|PILER-CR,CRISPRCasFinder,CRT,PILER-CR,PILER-CR,PILER-CR
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACGAAGCGAATAGAGAGCGTAGCTCGTTGTGCATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACCAAAGTGAAAGTTTAGAGTATTATTCTAAAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACACGAGTTTAGCACTATAACATCACTTTTAAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACGCATGTTCTGTAGCACCGACTATCTTCATAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACAGTATGTTTTTATATAAATGATTTAGAACAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACTGTGTTTCAGATGGCGAAGGGGATTATGATATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACTTTTCGCAAGAGGACAATTCAACCACCAGAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACCATACCATCTGAATTACATAGCACTTTATAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACAAACTCAGTCAAGTTGATGTCACCTGTAGTATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACGCAGGTAAACGCATTATGATTTCTTTGCGAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACTGTTATCTCATCATATTAGAAAAATAAACTATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACATGACAGGTGTATTTATAGCACTTGGAACAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACTACCTAAAAGAGCTGGACGCATACAGCTTGATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACACTAATTCTCAATTGAAATTCCAAAATGAGATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACATAGCTTACAAATGGTAAAAGCAGAATCAGATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACAAAGGTGTAATAAATGAATCTAAAACCAAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACCATAACTTTGTCGGAGGTGTTACGAAAAGTATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACGGTATAACTCAACTAATGGGGATGAATTAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACTATGAAAACATAATTGATAGCGTTCTGCGTATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACTAGACTTTTCGCCATCAAAACCTTTACGTTATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACTGTCCTACTGATATATTGATACTCATTTTTATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACAGACAAATTAGGAAATGAAATTACAAAAGAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACTAAGCACTATAACTTACCGATATGTTAATTATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACAGTAGTAGCTGATACGATACCGACTAAGAAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACGTACAAGCTGACTACTCATTCACTATGAAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACCCTTGTCTTAGCTTATTAGCTCTTTTTTGAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACAAAAGTGTTTTATGATCTAAATGCACCGGCATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACATGTTTGTTGGCAAAGAGCTTTTAACTAAAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACCGCGTGGGTACAAAACCCTAATTTAATTTATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACATGAGTAGAGTTACTTATTATTCATTAGATATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACCGCGTGGGTGCAAAACCCTAATTTAATTTATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACATGAGTAGAGTTACTTATTATTCATTAGATATTGTATCAAATGGGAATATTCATTACAACATTTAA

>NZ_CP043617|4|1|2137265-2137433|PILER-CR
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACGAAGCGAATAGAGAGC	GTAGCTCGTTGTGCATTGTATC
AAATGGGGATTTGAGAGTAGCTGAAGACCAAAGTGAAAGTTTAGAGTATTAT	TCTAAAATTGTATCAAATGGGGATTT
GAGAGTAGCTGAAGACACGAGTTTAGCACTATAACATCACTTTTAAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACGCATGTTCTGTAGCACCGACTATCTTCATAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGTATGTTTTTATATAAATGATTTAGAACA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTGTTTCAGATGGCGAAGGGGATTATGAT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TTTTCGCAAGAGGACAATTCAACCACCAGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACCATACCATCTGAATTACATAGCACTTTATAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAACTCAGTCAAGTTGATGTCACCTGTAGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GCAGGTAAACGCATTATGATTTCTTTGCGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTTATCTCATCATATTAGAAAAATAAACT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGACAGGTGTATTTATAGCACTTGGAACA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TACCTAAAAGAGCTGGACGCATACAGCTTG
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ACTAATTCTCAATTGAAATTCCAAAATGAG
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACATAGCTTACAAATGGTAAAAGCAGAATCAGATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAAGGTGTAATAAATGAATCTAAAACCAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CATAACTTTGTCGGAGGTGTTACGAAAAGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GGTATAACTCAACTAATGGGGATGAATTA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TATGAAAACATAATTGATAGCGTTCTGCGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TAGACTTTTCGCCATCAAAACCTTTACGTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTCCTACTGATATATTGATACTCATTTTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGACAAATTAGGAAATGAAATTACAAAAGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TAAGCACTATAACTTACCGATATGTTAATT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGTAGTAGCTGATACGATACCGACTAAGAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GTACAAGCTGACTACTCATTCACTATGAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CCTTGTCTTAGCTTATTAGCTCTTTTTTGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAAAGTGTTTTATGATCTAAATGCACCGGC
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGTTTGTTGGCAAAGAGCTTTTAACTAAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CGCGTGGGTACAAAACCCTAATTTAATTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGAGTAGAGTTACTTATTATTCATTAGAT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CGCGTGGGTGCAAAACCCTAATTTAATTT


>NZ_CP043617|4|4|2137265-2139341|CRISPRCasFinder
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GAAGCGAATAGAGAGCGTAGCTCGTTGTGC
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CAAAGTGAAAGTTTAGAGTATTATTCTAAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ACGAGTTTAGCACTATAACATCACTTTTAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GCATGTTCTGTAGCACCGACTATCTTCATA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGTATGTTTTTATATAAATGATTTAGAACA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTGTTTCAGATGGCGAAGGGGATTATGAT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TTTTCGCAAGAGGACAATTCAACCACCAGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CATACCATCTGAATTACATAGCACTTTATA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAACTCAGTCAAGTTGATGTCACCTGTAGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GCAGGTAAACGCATTATGATTTCTTTGCGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTTATCTCATCATATTAGAAAAATAAACT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGACAGGTGTATTTATAGCACTTGGAACA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TACCTAAAAGAGCTGGACGCATACAGCTTG
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ACTAATTCTCAATTGAAATTCCAAAATGAG
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATAGCTTACAAATGGTAAAAGCAGAATCAG
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAAGGTGTAATAAATGAATCTAAAACCAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CATAACTTTGTCGGAGGTGTTACGAAAAGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GGTATAACTCAACTAATGGGGATGAATTA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TATGAAAACATAATTGATAGCGTTCTGCGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TAGACTTTTCGCCATCAAAACCTTTACGTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTCCTACTGATATATTGATACTCATTTTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGACAAATTAGGAAATGAAATTACAAAAGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TAAGCACTATAACTTACCGATATGTTAATT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGTAGTAGCTGATACGATACCGACTAAGAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GTACAAGCTGACTACTCATTCACTATGAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CCTTGTCTTAGCTTATTAGCTCTTTTTTGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAAAGTGTTTTATGATCTAAATGCACCGGC
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGTTTGTTGGCAAAGAGCTTTTAACTAAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CGCGTGGGTACAAAACCCTAATTTAATTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGAGTAGAGTTACTTATTATTCATTAGAT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CGCGTGGGTGCAAAACCCTAATTTAATTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC

>NZ_CP043617|4|1|2137265-2139407|CRT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GAAGCGAATAGAGAGCGTAGCTCGTTGTGC
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CAAAGTGAAAGTTTAGAGTATTATTCTAAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ACGAGTTTAGCACTATAACATCACTTTTAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GCATGTTCTGTAGCACCGACTATCTTCATA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGTATGTTTTTATATAAATGATTTAGAACA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTGTTTCAGATGGCGAAGGGGATTATGAT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TTTTCGCAAGAGGACAATTCAACCACCAGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CATACCATCTGAATTACATAGCACTTTATA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAACTCAGTCAAGTTGATGTCACCTGTAGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GCAGGTAAACGCATTATGATTTCTTTGCGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTTATCTCATCATATTAGAAAAATAAACT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGACAGGTGTATTTATAGCACTTGGAACA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TACCTAAAAGAGCTGGACGCATACAGCTTG
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ACTAATTCTCAATTGAAATTCCAAAATGAG
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATAGCTTACAAATGGTAAAAGCAGAATCAG
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAAGGTGTAATAAATGAATCTAAAACCAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CATAACTTTGTCGGAGGTGTTACGAAAAGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GGTATAACTCAACTAATGGGGATGAATTA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TATGAAAACATAATTGATAGCGTTCTGCGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TAGACTTTTCGCCATCAAAACCTTTACGTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTCCTACTGATATATTGATACTCATTTTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGACAAATTAGGAAATGAAATTACAAAAGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TAAGCACTATAACTTACCGATATGTTAATT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGTAGTAGCTGATACGATACCGACTAAGAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GTACAAGCTGACTACTCATTCACTATGAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CCTTGTCTTAGCTTATTAGCTCTTTTTTGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAAAGTGTTTTATGATCTAAATGCACCGGC
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGTTTGTTGGCAAAGAGCTTTTAACTAAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CGCGTGGGTACAAAACCCTAATTTAATTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGAGTAGAGTTACTTATTATTCATTAGAT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CGCGTGGGTGCAAAACCCTAATTTAATTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGAGTAGAGTTACTTATTATTCATTAGAT
ATTGTATCAAATGGGAATATTCATTACAACATTTAA

>NZ_CP043617|4|2|2137529-2137762|PILER-CR
	GTAGCTCGTTGTGCATTGTATC
AAATGGGGATTTGAGAGTAGCTGAAGACCAAAGTGAAAGTTTAGAGTATTAT	TCTAAAATTGTATCAAATGGGGATTT
GAGAGTAGCTGAAGACACGAGTTTAGCACTATAACATCACTTTTAAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACGCATGTTCTGTAGCACCGACTATCTTCATAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGTATGTTTTTATATAAATGATTTAGAACA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTGTTTCAGATGGCGAAGGGGATTATGAT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TTTTCGCAAGAGGACAATTCAACCACCAGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACCATACCATCTGAATTACATAGCACTTTATAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAACTCAGTCAAGTTGATGTCACCTGTAGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GCAGGTAAACGCATTATGATTTCTTTGCGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTTATCTCATCATATTAGAAAAATAAACT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGACAGGTGTATTTATAGCACTTGGAACA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TACCTAAAAGAGCTGGACGCATACAGCTTG
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ACTAATTCTCAATTGAAATTCCAAAATGAG
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACATAGCTTACAAATGGTAAAAGCAGAATCAGATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAAGGTGTAATAAATGAATCTAAAACCAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CATAACTTTGTCGGAGGTGTTACGAAAAGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GGTATAACTCAACTAATGGGGATGAATTA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TATGAAAACATAATTGATAGCGTTCTGCGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TAGACTTTTCGCCATCAAAACCTTTACGTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTCCTACTGATATATTGATACTCATTTTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGACAAATTAGGAAATGAAATTACAAAAGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TAAGCACTATAACTTACCGATATGTTAATT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGTAGTAGCTGATACGATACCGACTAAGAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GTACAAGCTGACTACTCATTCACTATGAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CCTTGTCTTAGCTTATTAGCTCTTTTTTGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAAAGTGTTTTATGATCTAAATGCACCGGC
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGTTTGTTGGCAAAGAGCTTTTAACTAAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CGCGTGGGTACAAAACCCTAATTTAATTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGAGTAGAGTTACTTATTATTCATTAGAT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CGCGTGGGTGCAAAACCCTAATTTAATTT


>NZ_CP043617|4|3|2137793-2138224|PILER-CR
	GTAGCTCGTTGTGCATTGTATC
AAATGGGGATTTGAGAGTAGCTGAAGACCAAAGTGAAAGTTTAGAGTATTAT	TCTAAAATTGTATCAAATGGGGATTT
GAGAGTAGCTGAAGACACGAGTTTAGCACTATAACATCACTTTTAAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACGCATGTTCTGTAGCACCGACTATCTTCATAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGTATGTTTTTATATAAATGATTTAGAACA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTGTTTCAGATGGCGAAGGGGATTATGAT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TTTTCGCAAGAGGACAATTCAACCACCAGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACCATACCATCTGAATTACATAGCACTTTATAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAACTCAGTCAAGTTGATGTCACCTGTAGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GCAGGTAAACGCATTATGATTTCTTTGCGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTTATCTCATCATATTAGAAAAATAAACT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGACAGGTGTATTTATAGCACTTGGAACA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TACCTAAAAGAGCTGGACGCATACAGCTTG
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ACTAATTCTCAATTGAAATTCCAAAATGAG
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACATAGCTTACAAATGGTAAAAGCAGAATCAGATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAAGGTGTAATAAATGAATCTAAAACCAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CATAACTTTGTCGGAGGTGTTACGAAAAGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GGTATAACTCAACTAATGGGGATGAATTA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TATGAAAACATAATTGATAGCGTTCTGCGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TAGACTTTTCGCCATCAAAACCTTTACGTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTCCTACTGATATATTGATACTCATTTTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGACAAATTAGGAAATGAAATTACAAAAGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TAAGCACTATAACTTACCGATATGTTAATT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGTAGTAGCTGATACGATACCGACTAAGAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GTACAAGCTGACTACTCATTCACTATGAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CCTTGTCTTAGCTTATTAGCTCTTTTTTGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAAAGTGTTTTATGATCTAAATGCACCGGC
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGTTTGTTGGCAAAGAGCTTTTAACTAAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CGCGTGGGTACAAAACCCTAATTTAATTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGAGTAGAGTTACTTATTATTCATTAGAT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CGCGTGGGTGCAAAACCCTAATTTAATTT


>NZ_CP043617|4|4|2138255-2139341|PILER-CR
	GTAGCTCGTTGTGCATTGTATC
AAATGGGGATTTGAGAGTAGCTGAAGACCAAAGTGAAAGTTTAGAGTATTAT	TCTAAAATTGTATCAAATGGGGATTT
GAGAGTAGCTGAAGACACGAGTTTAGCACTATAACATCACTTTTAAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACGCATGTTCTGTAGCACCGACTATCTTCATAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGTATGTTTTTATATAAATGATTTAGAACA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTGTTTCAGATGGCGAAGGGGATTATGAT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TTTTCGCAAGAGGACAATTCAACCACCAGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACCATACCATCTGAATTACATAGCACTTTATAATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAACTCAGTCAAGTTGATGTCACCTGTAGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GCAGGTAAACGCATTATGATTTCTTTGCGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTTATCTCATCATATTAGAAAAATAAACT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGACAGGTGTATTTATAGCACTTGGAACA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TACCTAAAAGAGCTGGACGCATACAGCTTG
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ACTAATTCTCAATTGAAATTCCAAAATGAG
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGACATAGCTTACAAATGGTAAAAGCAGAATCAGATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAAGGTGTAATAAATGAATCTAAAACCAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CATAACTTTGTCGGAGGTGTTACGAAAAGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GGTATAACTCAACTAATGGGGATGAATTA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TATGAAAACATAATTGATAGCGTTCTGCGT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TAGACTTTTCGCCATCAAAACCTTTACGTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TGTCCTACTGATATATTGATACTCATTTTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGACAAATTAGGAAATGAAATTACAAAAGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	TAAGCACTATAACTTACCGATATGTTAATT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AGTAGTAGCTGATACGATACCGACTAAGAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	GTACAAGCTGACTACTCATTCACTATGAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CCTTGTCTTAGCTTATTAGCTCTTTTTTGA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	AAAAGTGTTTTATGATCTAAATGCACCGGC
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGTTTGTTGGCAAAGAGCTTTTAACTAAA
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CGCGTGGGTACAAAACCCTAATTTAATTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	ATGAGTAGAGTTACTTATTATTCATTAGAT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC	CGCGTGGGTGCAAAACCCTAATTTAATTT
ATTGTATCAAATGGGGATTTGAGAGTAGCTGAAGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP043617.1\|WP_152308117.1\|2143857_2144862_-\|phosphate-ABC-transporter-substrate-binding-protein-PstS	unknown	unknown	gnl\|CDD\|182837
NZ_CP043617.1\|WP_152308114.1\|2139676_2140828_+\|alcohol-dehydrogenase-catalytic-domain-containing-protein	unknown	unknown	gnl\|CDD\|176186
NZ_CP043617.1\|WP_152308122.1\|2148339_2150607_+\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|377162
NZ_CP043617.1\|WP_152308120.1\|2146795_2147581_+\|phosphate-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224042
NZ_CP043617.1\|WP_152308115.1\|2140817_2142422_-\|sodium:proton-exchanger	unknown	unknown	gnl\|CDD\|179625
NZ_CP043617.1\|WP_152308110.1\|2131512_2132256_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|187617
NZ_CP043617.1\|WP_152308105.1\|2127575_2128778_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP043617.1\|WP_152308104.1\|2125443_2127456_-\|BCCT-family-transporter	unknown	unknown	gnl\|CDD\|376718
NZ_CP043617.1\|WP_152308109.1\|2130968_2131430_-\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197670
NZ_CP043617.1\|WP_152308111.1\|2132425_2135899_+\|type-II-CRISPR-RNA-guided-endonuclease-Cas9	cas9	cd09643_cas9_CAS-II-A:CAS-II-B:CAS-II-C	gnl\|CDD\|187774
NZ_CP043617.1\|WP_152308106.1\|2128755_2129661_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|377694
NZ_CP043617.1\|WP_152308121.1\|2147595_2148267_+\|PhoU-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|273990
NZ_CP043617.1\|WP_152308119.1\|2145860_2146700_+\|phosphate-ABC-transporter-permease-PstA	unknown	unknown	gnl\|CDD\|183065
NZ_CP043617.1\|WP_152308118.1\|2145003_2145861_+\|phosphate-ABC-transporter-permease-subunit-PstC	unknown	unknown	gnl\|CDD\|223646
NZ_CP043617.1\|WP_152308116.1\|2142559_2143693_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP043617.1\|WP_152308112.1\|2136013_2136886_+\|type-II-CRISPR-associated-endonuclease-Cas1	cas1	cd09720_cas1_CAS-II-A:CAS-II-B:CAS-II-C	gnl\|CDD\|274694
NZ_CP043617.1\|WP_152308107.1\|2129872_2130211_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227262
NZ_CP043617.1\|WP_152308123.1\|2150652_2151393_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP043617.1\|WP_152308108.1\|2130222_2130957_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|380375
NZ_CP043617.1\|WP_152308113.1\|2136882_2137215_+\|CRISPR-associated-endonuclease-Cas2	cas2	COG3512_cas2_CAS-II-A:CAS-II-B:CAS-II-C	gnl\|CDD\|226043

Protein	Function_ID	Function_description	E-value
NZ_CP043617.1\|WP_152308117.1\|2143857_2144862_-\|phosphate-ABC-transporter-substrate-binding-protein-PstS	gnl\|CDD\|182837	PRK10918, PRK10918, phosphate ABC transporter substrate-binding protein PstS.	8.81042e-110
NZ_CP043617.1\|WP_152308114.1\|2139676_2140828_+\|alcohol-dehydrogenase-catalytic-domain-containing-protein	gnl\|CDD\|176186	cd05283, CAD1, Cinnamyl alcohol dehydrogenases (CAD). Cinnamyl alcohol dehydrogenases (CAD), members of the medium chain dehydrogenase/reductase family, reduce cinnamaldehydes to cinnamyl alcohols in the last step of monolignal metabolism in plant cells walls. CAD binds 2 zinc ions and is NADPH- dependent. CAD family members are also found in non-plant species, e.g. in yeast where they have an aldehyde reductase activity. The medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family, which contains the zinc-dependent alcohol dehydrogenase (ADH-Zn) and related proteins, is a diverse group of proteins related to the first identified member, class I mammalian ADH. MDRs display a broad range of activities and are distinguished from the smaller short chain dehydrogenases (~ 250 amino acids vs. the ~ 350 amino acids of the MDR). The MDR proteins have 2 domains: a C-terminal NAD(P) binding-Rossmann fold domain of a beta-alpha form and an N-terminal catalytic domain with distant homology to GroES. The MDR group contains a host of activities, including the founding alcohol dehydrogenase (ADH), quinone reductase, sorbitol dehydrogenase, formaldehyde dehydrogenase, butanediol DH, ketose reductase, cinnamyl reductase, and numerous others. The zinc-dependent alcohol dehydrogenases (ADHs) catalyze the NAD(P)(H)-dependent interconversion of alcohols to aldehydes or ketones. Active site zinc has a catalytic role, while structural zinc aids in stability. ADH-like proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and generally have 2 tightly bound zinc atoms per subunit. The active site zinc is coordinated by a histidine, two cysteines, and a water molecule. The second zinc seems to play a structural role, affects subunit interactions, and is typically coordinated by 4 cysteines.	3.31119e-168
NZ_CP043617.1\|WP_152308122.1\|2148339_2150607_+\|diguanylate-cyclase	gnl\|CDD\|377162	pfam03924, CHASE, CHASE domain. This domain is found in the extracellular portion of receptor-like proteins - such as serine/threonine kinases and adenylyl cyclases. Predicted to be a ligand binding domain.	1.09057e-70
NZ_CP043617.1\|WP_152308120.1\|2146795_2147581_+\|phosphate-ABC-transporter-ATP-binding-protein	gnl\|CDD\|224042	COG1117, PstB, ABC-type phosphate transport system, ATPase component [Inorganic ion transport and metabolism].	7.23855e-154
NZ_CP043617.1\|WP_152308115.1\|2140817_2142422_-\|sodium:proton-exchanger	gnl\|CDD\|179625	PRK03659, PRK03659, glutathione-regulated potassium-efflux system protein KefB; Provisional.	7.76907e-83
NZ_CP043617.1\|WP_152308110.1\|2131512_2132256_+\|SDR-family-oxidoreductase	gnl\|CDD\|187617	cd05359, ChcA_like_SDR_c, 1-cyclohexenylcarbonyl_coenzyme A_reductase (ChcA)_like, classical (c) SDRs. This subgroup contains classical SDR proteins, including members identified as 1-cyclohexenylcarbonyl coenzyme A reductase. ChcA of Streptomyces collinus is implicated in the final reduction step of shikimic acid to ansatrienin. ChcA shows sequence similarity to the SDR family of NAD-binding proteins, but it lacks the conserved Tyr of the characteristic catalytic site. This subgroup also contains the NADH-dependent enoyl-[acyl-carrier-protein(ACP)] reductase FabL from Bacillus subtilis. This enzyme participates in bacterial fatty acid synthesis, in type II fatty-acid synthases and catalyzes the last step in each elongation cycle. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRS are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes have a 3-glycine N-terminal NAD(P)(H)-binding pattern (typically, TGxxxGxG in classical SDRs and TGxxGxxG in extended SDRs), while substrate binding is in the C-terminal region. A critical catalytic Tyr residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering), is often found in a conserved YXXXK pattern. In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) or additional Ser, contributing to the active site. Substrates for these enzymes include sugars, steroids, alcohols, and aromatic compounds. The standard reaction mechanism is a proton relay involving the conserved Tyr and Lys, as well as Asn (or Ser). Some SDR family members, including 17 beta-hydroxysteroid dehydrogenase contain an additional helix-turn-helix motif that is not generally found among SDRs.	8.16492e-70
NZ_CP043617.1\|WP_152308104.1\|2125443_2127456_-\|BCCT-family-transporter	gnl\|CDD\|376718	pfam02028, BCCT, BCCT, betaine/carnitine/choline family transporter.	0
NZ_CP043617.1\|WP_152308109.1\|2130968_2131430_-\|MarR-family-transcriptional-regulator	gnl\|CDD\|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	5.91105e-18
NZ_CP043617.1\|WP_152308111.1\|2132425_2135899_+\|type-II-CRISPR-RNA-guided-endonuclease-Cas9	gnl\|CDD\|187774	cd09643, Csn1, CRISPR/Cas system-associated protein Cas9. 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; Very large protein containing McrA/HNH-nuclease related domain and a RuvC-like nuclease domain; signature gene for type II.	1.01342e-63
NZ_CP043617.1\|WP_152308106.1\|2128755_2129661_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|377694	pfam06719, AraC_N, AraC-type transcriptional regulator N-terminus. This family represents the N-terminus of bacterial ARAC-type transcriptional regulators. In E. coli, these regulate the L-arabinose operon through sensing the presence of arabinose, and when the sugar is present, transmitting this information from the arabinose-binding domains to the protein's DNA-binding domains. This family might represent the N-terminal arm of the protein, which binds to the C-terminal DNA binding domains to hold them in a state where the protein prefers to loop and remain non-activating. All family members contain the pfam00165 domain.	2.07638e-44
NZ_CP043617.1\|WP_152308121.1\|2147595_2148267_+\|PhoU-family-transcriptional-regulator	gnl\|CDD\|273990	TIGR02135, Uncharacterized_protein, phosphate transport system regulatory protein PhoU. This model describes PhoU, a regulatory protein of unknown mechanism for high-affinity phosphate ABC transporter systems. The protein consists of two copies of the domain described by pfam01895. Deletion of PhoU activates constitutive expression of the phosphate ABC transporter and allows phosphate transport, but causes a growth defect and so likely has some second function. [Regulatory functions, Other, Transport and binding proteins, Anions].	2.53144e-14
NZ_CP043617.1\|WP_152308119.1\|2145860_2146700_+\|phosphate-ABC-transporter-permease-PstA	gnl\|CDD\|183065	PRK11268, pstA, phosphate ABC transporter permease PstA.	2.82194e-114
NZ_CP043617.1\|WP_152308118.1\|2145003_2145861_+\|phosphate-ABC-transporter-permease-subunit-PstC	gnl\|CDD\|223646	COG0573, PstC, ABC-type phosphate transport system, permease component [Inorganic ion transport and metabolism].	5.25805e-89
NZ_CP043617.1\|WP_152308112.1\|2136013_2136886_+\|type-II-CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|274694	TIGR03639, cas1_NMENI, CRISPR-associated endonuclease Cas1, subtype II/NMENI. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is a prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes the Cas1 variant of the NMENI subtype of CRISPR/Cas system.	7.6434e-80
NZ_CP043617.1\|WP_152308107.1\|2129872_2130211_+\|hypothetical-protein	gnl\|CDD\|227262	COG4925, COG4925, Uncharacterized conserved protein [Function unknown].	9.65458e-44
NZ_CP043617.1\|WP_152308108.1\|2130222_2130957_+\|hypothetical-protein	gnl\|CDD\|380375	cd02910, cupin_Yhhw_N, Escherichia coli YhhW and YhaK and related proteins, pirin-like bicupin, N-terminal cupin domain. This family includes the N-terminal cupin domains of YhhW and YhaK, Escherichia coli pirin-like proteins with unknown function. YhhW is structurally similar not only to human pirin but also to quercitin 2,3-dioxygenase (quercitinase). Although the function of YhhW is not completely understood, YhhW and its human ortholog have quercitinase activity and are likely to play an important role in transcription and apoptosis. This N-terminal cupin domain of YhhW has a metal coordination site and is thought to have catalytic activity while the C-terminal cupin-like domain has diverged considerably and has closer alignment with C-terminal pirin. YhaK is found in low abundance in the cytosol of E. coli and is strongly up-regulated by nitroso-glutathione (GSNO). There are major structural differences at the N-terminus of YhaK compared with YhhW; YhaK lacks the canonical cupin metal-binding residues of pirins and may be involved in chloride binding and/or sensing of oxidative stress in enterobacteria. YhaK showed no quercetinase and peroxidase activity; however, reduced YhaK was very sensitive to reactive oxygen species (ROS). Proteins in this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold.	7.09596e-16
NZ_CP043617.1\|WP_152308113.1\|2136882_2137215_+\|CRISPR-associated-endonuclease-Cas2	gnl\|CDD\|226043	COG3512, COG3512, CRISPR-associated protein, Cas2 homolog [Defense mechanisms].	9.74278e-22

>NZ_CP043617.1|WP_152308113.1|2136882_2137215_+|CRISPR-associated-endonuclease-Cas2
MSRFRRMVLFAMFDMPTETKGDLKRYRQFRKDLLSYGFIMFQYSVYVRFCDSLYMAEKYEAKIEEVAPEKSSIRVLRVTENQYKNMIIVENYREKPEEKVEEMTQLVMVF
>NZ_CP043617.1|WP_152308112.1|2136013_2136886_+|type-II-CRISPR-associated-endonuclease-Cas1
MFKHIFIKNRSHLYYKNNSLGIKNDDFDTTISLDDIDMLIVENQQTTITSSLLSHLAQKNICTVFVDEKYMPSSINIPLYKNSRVSLVQKAQQKVSKPKHNQLWKQIIFAKIKHQSFVLEKYKKSKAIDGLWHKVTSADKTNIEALAANIYFPELFGKEFTRRDDSVINAALNYGYSIIRSSIARYIIAYGINPTNGIFHSSQLNNFNLADDFIEVFRPVVDEFVHCNIKSKSFGWEEKKKFSVLLYEYELFNIEEERKISLDNAIKTVVASYQSFCLGKRENINIAKMI
>NZ_CP043617.1|WP_152308111.1|2132425_2135899_+|type-II-CRISPR-RNA-guided-endonuclease-Cas9
MKRVLGLDIGVASIGFSLIDVLEKDGKTEFNNLTTNSIIFDVPELAEERRKGRSSRRLNDRKSRRKQHIRNLFFEHGLTDKSFVTEPSSYLNTLDVESDVYILREKALHQDLSKAEFIKALYSITTRRGYSNQFESTEQDENSAKENEKINGSISKNIQLIKEKGFILPTELLTYRRTQKEELGYQNIPVRNKGGNYTNSLNRKLHEDELKIVIFSQKDNRNIFASEEKCEKFYIAVRDVMMEQRPLKSFEDMVAYCSYFDKYHETPQKRMSLSSIYNIELTLKQSLSNYKTMDKKSGEIISLSKKQIDEVVAKWVNEPTSDKITFANIFTKTSLKNCKLNDVGGSAEVLNIKGFRELSAIFKQYNVDFYTEHRDFFEKALLILSYYKNISKRVEELQKSFTGKLEPKDEFINEVAKVSSIDGFGSFSVRFAKMVLEKMEQGNSFSEALESLGYFDKYLGMPAYDYLPPFNPTQADIKWLKENLSYFDTKHLYYKANSSKTVERIISVMRKLINDIIKKYGKIDEIAIEGGKELNSKKEEDKIKENQKDDKKINDEAKNLLKDKNIKDYDNPTKVRKAKMLIEQKYKCLYSNEPLTLKEALDEEECEIEHFIPRSHFWNNSQKNTILVLKKHNQNKTDVPPMEYLKQIGKWEDYKAAVHNSSMKESKKDWLTNEEKIEAIFDQDTNVFLANYLNDTRSSIKIIKNYLEHYLYPKTNRYGKDEQSNVRVVSAKAINELKHIWGIKELITSEDTGKKDRTTNYHHSIDALTVALCDKKGMFALHNFFKQKENKFKTKAMKENVSKNVPFTSEGETLHSFCSHLVEKYKNNELYVCPYNKIKTNKKGFKDGNKKLVVAQNSKGVKQLQELKNISLLPYDLLQEKKQLKVTDRTDEGVRMCVQEIVSQLDIFKQKGIREALPKYGEFLIAKRAEEEKFSVLEKELVNKQKADKKKEDVELSKQIDEIKSQLQSVRDEIAFSNCYFVTKNGTKQIVKGVKNLSDSETKASTVLIQNGNSILMEKLNIETFKQAQEEGHPFVCKENDYTVSVDIYSSSKHQIIGLKYFRSIENDIEPNFKESFQNIDKQYEFSIHKGEVVVILDEKEKVQYLAVANGGGQIAGTNHKIQIENINTNGVVAVTINKKTIIKKAKIDFYGNFQIG
>NZ_CP043617.1|WP_152308110.1|2131512_2132256_+|SDR-family-oxidoreductase
MSKKNVLITGGARGIGAATAKELGAQGYRVFINYVNSTQVANELVDEINSNGGEAYAIQADVRVDTQVESMFDDIESKYGGVDILVSNANMNFTQKPFVEQTWDEFSQKLNDEMHAAYVSAKYATTSMIKKKFGRLVFISSTLSESPAPSFIAHGSAKGALDTFSKYLAQELGAHGITSNIIAPGLVLTDATSQAPDEFKEFIRSMTPTQTISKPEDVANAISFLVKDESAQVTGAYLSVSGGAYLS
>NZ_CP043617.1|WP_152308109.1|2130968_2131430_-|MarR-family-transcriptional-regulator
MCYNFLMKKEEFNLSESYGYHFNIIFTNIKRMMESRLKIYDATHLQFSILVNLYKNNVKTQKEMLKYVNGDEASITRLIDRLESKGLIKRVKSTEDKRKKHLVLTHSGVSLAKKTIACAQEVNQEIIKDLDKDEAKKLLELLQKVHLSLDKLE
>NZ_CP043617.1|WP_152308108.1|2130222_2130957_+|hypothetical-protein
MLLHKSKSDQQIQHLFNNSFTENKPIPFPEHNKHYAYSSLFYWAHLVAHESAEFPLHGHKGFEIMTFVLKGSLEHFDTATNVWTPIKQGGFQIIQAGSGVMHSERIVKGSEVFQIWFDPDFSKTLKTDPSYQDYTEDNLSIDNAENVKAIEYIGTKSDIEHQTADISIRREFFQKGTYTKKTGISYVYSIYVMEGEGSINKKSVVQDDFVVIDDTSSFVVDAKDELELFIIKSPKVLPYPRVKI
>NZ_CP043617.1|WP_152308107.1|2129872_2130211_+|hypothetical-protein
MQITIESNGEKTIFELNDSDAAKELYTQLPLNIDVENFGSNEKIFYPPKKLSTSNTPPANAKNGTLAYYAPWGDVVMFYKDFGAAKGLYELGSCISACENIKNMSGTINIHK
>NZ_CP043617.1|WP_152308106.1|2128755_2129661_-|helix-turn-helix-domain-containing-protein
MHSNLEKLRSEMIDFLSATYPLEGDVQSEISNLDFFFSKSPTQQINILYEPSLCVILQGHKAVGFGDETLSYDNEEYLISSTHLPAKMKILEASEDKPYMSLRVKFSLEDIYELLKTLKPHEEKLDKNAQKGLYFGDMDIELYESIHRFIMLLKRPKEDIEYLSPLLVKEILYNLVKSKGGTFLRKFSQAGTTSNKITKVISQIKENFDEKLNIKELAYSVDMSESSLYQHFKTITTMSPIQFQKNLRLEEAKQLLLLKDIEISEAAFQVGYESPSQFSREFSRMFGLSPKAYILKNNIQN
>NZ_CP043617.1|WP_152308105.1|2127575_2128778_+|hypothetical-protein
MKRPNKFLSLSLSFLATSCFLEASSSYNSIKIGDFSLGGALRVNYVNDSSKTDTANASKGSQGIFDLDTARVNIDYKHDDFLGKFEYRWYPGFGNTQNGTNYSFIHTAWLGYAINNTAHVEVGINRVPFGPTAYGASQSWFFDQHYYVGLADDMDLGVKFSSTLNNIKYDLAYYYGSEDDGIGAGGESTRYAYDVVDDFHEKNQLSARVIYSSKLWDKKQEYGISLLYSQLEAQTQGVDDGSRFAVSAHMINRYKNFTLTTQLTRYEMSVDANNDSVDDALIKMGGFNYGEGVASEAWLPSVSLNYKIDTPNIEWLDYALPYIEYSNIIKDEDTFNNSYMWMIGTAFARGNWYIYTDLALANGNYFVGPYTGSDGGTNNFGANSSNDLEHRLNINFGYYF
>NZ_CP043617.1|WP_152308104.1|2125443_2127456_-|BCCT-family-transporter
MEESEASKSRESTILKPVFYPSVAVIFIMVVFAVIDPQDVGEIFSSIKQFIAQKFGWLYMLSVGVFTFFVLFLALSPYGRFKLGPDQSKPNFSYSSWFAMLFSAGMGIGLMFWSVAEPVMHYTSPPIGDGGTMQAAKDAMKITFFHWGFHAWAIYAVVGLVLAYFSFRHGLPLSVRSALYPLVGKKIYGSIGHTVDTVAVLGTILGVATSLGLGVMQVNAGLNYLFDITISTSVQVVLIAIITAMATVSVVLGLEGGIKKLSNLNLYLAASLLLFVLLAGPTFFLLDAWLQNIGNYLSDIVYMTFNQYAYNDTKWMSSWTLFYWAWWIAWAPFVGMFIARVSRGRTIREFVFGVMFVPVGFTFIWMTVFGNTALDAIMNNGFVALSEAVSADVSTALFKFLEHFPMSSFVSVVAMILVITFFVTSSDSGSLVVDTIASKTKLEAPVWQRIFWAVLEGVVAATLLLAGGLGALQSASITIALPFAVIMLIASWGLYRALHLESTRYESLQHHMNAGRHGKISGTWKSRLSRIVSYPSMQETKRFISEDVMNAMKLVKDELNTHYWDVEIIHDNKNSVSFFKAEHSGDMDFIYEVRAKKYDTPEYAFPESINPTQEQHEYARAEVYLQDGNKAYDIYGYDEEVIATDIIDQFEKHRHFLHNTAGLSPAIPID
>NZ_CP043617.1|WP_152308114.1|2139676_2140828_+|alcohol-dehydrogenase-catalytic-domain-containing-protein
MQTSQNPSRRDFIKTSAAIGAGLILWSPVLATDKGDKMNAITTKGYAAFDESGVLKPWTFTRRPVGDNDVLIDIKFASICHSDIHQEKGHWGKQQYPQVPGHEIAGVVTAVGKNVTKFKVGDRAGVGCMVDGCTTCENEEQYQSDTLFTYGYPDKREPTRISQGGYSKQIVVRDHYVVHIPDSLSFENAAPLLCAGITTYSPIMRADFKKGDKVAVAGIGGLGHMAVKFALSRGAEVYAFTTSADKVEDIKAFGVKEVIVVDDTKKLYEYAGQMDYMICTIPYQFDVAAYASVVKPYGFFTQVGMPEAFEITLNNLGLSFSRVNFNASLIGGMKETQEVVDYCAENKIYPQIEIIDAKDITDAWKKVENKQARFRYVIDTATI
>NZ_CP043617.1|WP_152308115.1|2140817_2142422_-|sodium:proton-exchanger
MLEIIIFSILSATILNLFLKKFSIPTIIGYIATGTIIAYGYELHDAINSHELKEIAEFGVVFLMFTIGLEFSVRNLIKMKKEVFLYGALQVFITAAFFSFLAHNIFSIEAKSSIIIGAALALSSTAIVLKLLNENGDINKLYGRKVLGILLFQDIAVIPILLMITMFSVTDKSVSSLLIETLLNAVVLLMGLFLVGKYLIEPFFHQVSKTKSNEIFVGSVLLIVMGASYLAHAFGFSYSLGAFIAGMMIAETHYKHQVEADLVPFRDLLLGVFFVTVGMQLNFSIIFENIYTVLLILPVLILAKILIIYLLLRFATDSRVALKSAITLFQFGEFGLVIFELSFAKNLIDPVIGQVLVVMVVISMIMTPFVLKNISKIVDMFSYTPEESQEYTSPDNNEKLSNHIVLIGYGRLGKNISRLIEKKNMDYIAIENDILSVKEARKLNKPVIFGNAAQKNVLESVNIKDASAVVISIGNSEKLHQICQAVKDLRENKKTIVKVNKYEEQEALSSLNLSHIIVETEKTASAMFEEAIKL
>NZ_CP043617.1|WP_152308116.1|2142559_2143693_-|hypothetical-protein
MKKIILSAVAGLTLASSVMASDATPVFSHTDKLKFSGLTYIGLTKNSYKDELVNPNETNFELRRAYFQLKAYLLDDPKSYYRVTFDMHQNAEDDMVVRAKYAYLYLNNVLENTGVELGLVHRPWHDYEEHNAWFYRDISKVMIEAKNGGDLSNSADFGFNFKTKTQYFDSEIGIFNGEGYHSDFNDDEASDKAGNGMSLEWRATAHILGVNGKDKQTKKTYFDASFFGQYNQEHKASASGLANDYDDLVFYGLHTVYNQPEFLVSAQYVVSDDTADNSTYVSAQAGSGYSINGEYRFGNTYEYRVLARYDAWTDEELVSSDERERTSLIAGFAWQQNHNVQWVANVIVKDNEKDAFKASKPEKADSTAYMLTAQVEF
>NZ_CP043617.1|WP_152308117.1|2143857_2144862_-|phosphate-ABC-transporter-substrate-binding-protein-PstS
MLKKILSTLLVAAVGVTPLLAADKINGAGASFPAPLYYGWAFDYRKDTKNRVNYQSIGSGGGIKQITKRVVDFGASDKPLNAKKLSKGKLLQFPAVIGSIVVAFNIDGIADATLKLKNDVVADIFAGRITKWNDAAIKADNPDINLPDAKIIVVHRSDGSGTTYNFTYYLSGSSKNWKENFGTGKAIDWATGIGGKGNEGVANLIKQTPNSIGYIENAYKEKNHLSAAVLKTASGKWVQATEANFKAAAKYASWTKKDHFYAMLALQPGDTSYPIVAATFILLPIEKPKMNKKVIKFYDYAFMNGDAQAKKLGYIALPDATKKMIREYWAENIK
>NZ_CP043617.1|WP_152308118.1|2145003_2145861_+|phosphate-ABC-transporter-permease-subunit-PstC
MSLIIDKFFANSTKLIAVGILLLVASIFAILFEHSLTSIQAFGVSFVTETKWAPNLEKFGALPAIYGSVLSTFLAMILAVPVAIGVAIFLSELAPAKLKSPVGVSIELLAAIPSVIYGMWGLFYFVPIVRDAVGGIGISMLTAGIVLSIMILPFMAAVTRDAMNTTPDILKESAYALGGTKWDVIKDIVIPYAKAGIIGSFILALGRAIGETMAVTFVMGNVHKVSTDLTQPATSIPVTLANEFTEADTDLYYSSLFELSLLLLVISFTIIFVAKFYFLRRKKAV
>NZ_CP043617.1|WP_152308119.1|2145860_2146700_+|phosphate-ABC-transporter-permease-PstA
MTQTQKRILTNKIVMSLSTLSALIGMGFLFWILYVLVFNGVDALSSTIFTSEGAPPGYEQSGLKHALIGQLYIVGYATIFGVPLGILAGTYLSEYGGRAKLAEIIRDISDIMMSAPSIVIGAFVYAIVVAPMGHFSGWAGSVALTIIMIPIILRTTDDMLQLVPSTLREAAFALGAPKYKVIIQVVYRGAKAGILTGILLGVARVAGETAPLLFTSFNDNFLNTDMMEPMASLTVTMYNYATSPYEDWQRLGWAAAFILSMFILGLNIIGRLFIMKKKS
>NZ_CP043617.1|WP_152308120.1|2146795_2147581_+|phosphate-ABC-transporter-ATP-binding-protein
MASIVDINGEIALDVKDFDFTYASAEEASIKKVSMPIAKNSITALIGPSGCGKTTLLRSFNRMHDLYPGNKYDGEVMFKGRNILSAKEDLINLRIQIGMIFQKPTAFPMSIFDNVAYGMRLQGIKNKTELQDRVEKALKDAAIFKEVKDRLKHDANGLSGGQQQRLCIARAIAVEPEVLLFDEPTSALDPISTAGIEELVVSLKDRVSIVIVTHNMQQAARVSDYTGFMYLGELIELGKTEELFVTPREKLTQDYITGKFG
>NZ_CP043617.1|WP_152308121.1|2147595_2148267_+|PhoU-family-transcriptional-regulator
MRSKYEIKITDIREKIAKLLENITQANKIAYDAYKDNDTIKFQEVQDKLNNLGFNADMIDNEIIKAFALFGPEADELRSLIAYLKMTNEIVRIGMGIKKYARRMKEHIDSECDLEPLNPTILPLHKSTIASLELICECFVNFDECNIEDNYRKVMVEESKNDDLFSILEKDIMTNIIDEKELAIEYVKVLGSLRKLERSCDRTVNIANLMLYAKNGGEIHLHQ
>NZ_CP043617.1|WP_152308122.1|2148339_2150607_+|diguanylate-cyclase
MPIHFNKSHKVWPIVTIIIGLLFSALSGWLTYNYYKEKENLRLDLASNEIILLVQNRMAAYEQVLKSGVGLFNASDMVSRKEWTIFVKEHKLNENFKGIQGFGYSEVVLPQNKHQHEERIRKEGFADFKIYPDGKRELYTSIIYLEPFDERNIRAFGYDMFSEKIRRIAMKKAMLNGKAALSGKIKLVQEFNTDIQAGFLMYLPVYKKGYKLDTPQERALAIQGFVYAPFRANDLMNGILGKMFPNIDFEIYDGDSIAKDNILYSSNSNNKSKLYKKTNITMNGHTWTLIFKTNSVFKSENIYVIFLIPSLILILTFLLYSLLNSLIKTEKNAVQIAKKATQKLQNSEERLRYALEGAGDGLWDWNLVTDEVFFSKRWKKMLGFSEDEIGSDIDEWKSLIHPEDLEHMDADITAHIEGKRDTYKNEHRVKCKDGSYKWILDRGIIVSRSIDGTPLRMVGSQSDISERKQSQLKLAYYLEIIDKNVISSTTDLHGKITKVSQAFSDISGYSKNELLGKSHNILRHKDMPSSTYKELWKTIQSGNIWEGEIKNKRKDGSTYWVDATISPVKNEQGETINYTSIRHDITDKKRIEELSVTDKLTQLYNRLKLDEIFSMKLASARRYNSTFSIIMMDIDYFKSVNDTWGHQAGDDILKEFATIIKNNIRETDVVGRWGGEEFLILSSESDLESAIKLSEKLRDIVSLFKFSFAGHKTASFGVSSYHAGDDEKTMVKRADDALYRAKENGRNRVEVEKYD
>NZ_CP043617.1|WP_152308123.1|2150652_2151393_-|hypothetical-protein
MVYDFWKNYEELLSYEQASLLDYRLDNISIKLNEFFQRLIITHIKKRYIKFYLAGSCIKADRFRDLDMFFPFNEDRELLNSAMNQDFFEYENNSYTYKYKNDIYQLVYRERFEGASLKELVEGFDFDSTKIAFECVYDTKKRLFSILECDMRIEFVNYINTRINHLTRVSVNPFVSLQRAIYFLKRGDDVPYDVFLQVCSKIADLKVEEDKDTSKHFQNLQGNPNKLSNIKEAISHYIDEQKDSHK

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP043617_4	4.9\|2137697\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137697-2137726	30	NZ_CP043617.1	587969-587998	0	1.0

1. spacer 4.9|2137697|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to position: 587969-587998, mismatch: 0, identity: 1.0

ttttcgcaagaggacaattcaaccaccaga	CRISPR spacer
ttttcgcaagaggacaattcaaccaccaga	Protospacer
******************************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP043617_4	4.2\|2137391\|26\|NZ_CP043617\|PILER-CR	2137391-2137416	26	NZ_CP048772	Campylobacter jejuni strain ZS007 plasmid pCJ145K, complete sequence	112828-112853	3	0.885
NZ_CP043617_4	4.2\|2137391\|26\|NZ_CP043617\|PILER-CR	2137391-2137416	26	NZ_MK275621	Clostridium perfringens strain JXJA17 plasmid p3, complete sequence	14813-14838	3	0.885
NZ_CP043617_4	4.2\|2137391\|26\|NZ_CP043617\|PILER-CR	2137391-2137416	26	NZ_CP014857	Lysinibacillus sphaericus III(3)7 plasmid, complete sequence	66805-66830	4	0.846
NZ_CP043617_4	4.2\|2137391\|26\|NZ_CP043617\|PILER-CR	2137391-2137416	26	NZ_CP014644	Lysinibacillus sphaericus strain OT4b.25 plasmid unnamed, complete sequence	32445-32470	4	0.846
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	AP013392	Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C6A-MedDCM-OCT-S43-C64	7130-7159	5	0.833
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	AP013391	Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C6A-MedDCM-OCT-S33-C54	3911-3940	5	0.833
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	AP013390	Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C6-MedDCM-OCT-S27-C41	21879-21908	5	0.833
NZ_CP043617_4	4.4\|2137367\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2137367-2137396	30	NZ_CP014644	Lysinibacillus sphaericus strain OT4b.25 plasmid unnamed, complete sequence	32445-32474	6	0.8
NZ_CP043617_4	4.4\|2137367\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2137367-2137396	30	NZ_CP014857	Lysinibacillus sphaericus III(3)7 plasmid, complete sequence	66801-66830	6	0.8
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	MN694255	Marine virus AFVG_250M362, complete genome	22646-22675	6	0.8
NZ_CP043617_4	4.14\|2138027\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138027-2138056	30	NZ_CP028882	Borreliella bavariensis PBi plasmid lp28-3, complete sequence	5011-5040	6	0.8
NZ_CP043617_4	4.17\|2138225\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2138225-2138254	30	AP013543	Uncultured phage_MedDCM-OCT-S30-C28 DNA, complete genome, group G8, isolate: uvMED-CGR-U-MedDCM-OCT-S30-C28	7359-7388	6	0.8
NZ_CP043617_4	4.18\|2138291\|29\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138291-2138319	29	KY653124	Staphylococcus phage IME1367_01, complete genome	5994-6022	6	0.793
NZ_CP043617_4	4.18\|2138291\|29\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138291-2138319	29	MK554696	Fusobacterium phage Fnu1, complete genome	124245-124273	6	0.793
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	NC_022778	Clostridium tetani 12124569 plasmid p12124569, complete sequence	7648-7677	6	0.8
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	KP836356	Marinitoga camini virus 2, complete genome	27307-27336	6	0.8
NZ_CP043617_4	4.29\|2139014\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2139014-2139043	30	NC_008382	Rhizobium leguminosarum bv. viciae 3841 plasmid pRL7, complete sequence	84505-84534	6	0.8
NZ_CP043617_4	4.31\|2139146\|29\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2139146-2139174	29	NZ_AP017296	Nostoc sp. NIES-3756 plasmid pNOS3756_1, complete sequence	266900-266928	6	0.793
NZ_CP043617_4	4.4\|2137367\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2137367-2137396	30	NZ_CP048772	Campylobacter jejuni strain ZS007 plasmid pCJ145K, complete sequence	112824-112853	7	0.767
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	MN693159	Marine virus AFVG_25M303, complete genome	16382-16411	7	0.767
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	NC_014839	Pantoea sp. At-9b plasmid pPAT9B02, complete sequence	81514-81543	7	0.767
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	NZ_CP009368	Bacillus cereus strain FM1 plasmid unnamed, complete sequence	120974-121003	7	0.767
NZ_CP043617_4	4.13\|2137961\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137961-2137990	30	AP014137	Uncultured Mediterranean phage uvMED isolate uvMED-GF-C47-MedDCM-OCT-S35-C41, * SEQUENCING IN PROGRESS *	18444-18473	7	0.767
NZ_CP043617_4	4.16\|2138159\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138159-2138188	30	NZ_CP049297	Bacillus megaterium strain S188 plasmid pS188, complete sequence	76801-76830	7	0.767
NZ_CP043617_4	4.16\|2138159\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138159-2138188	30	NZ_CP045274	Bacillus megaterium strain FDU301 plasmid pFDU301B, complete sequence	147937-147966	7	0.767
NZ_CP043617_4	4.17\|2138225\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2138225-2138254	30	MK250029	Prevotella phage Lak-C1, complete genome	305453-305482	7	0.767
NZ_CP043617_4	4.17\|2138225\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2138225-2138254	30	MK250016	Prevotella phage Lak-A1, complete genome	339427-339456	7	0.767
NZ_CP043617_4	4.17\|2138225\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2138225-2138254	30	MK250019	Prevotella phage Lak-A2, complete genome	260094-260123	7	0.767
NZ_CP043617_4	4.18\|2138291\|29\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138291-2138319	29	MN855613	Siphoviridae sp. isolate 60, complete genome	650-678	7	0.759
NZ_CP043617_4	4.19\|2138356\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138356-2138385	30	NZ_CP015602	Pseudomonas antarctica strain PAMC 27494 plasmid pP27494_2, complete sequence	19483-19512	7	0.767
NZ_CP043617_4	4.22\|2138553\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138553-2138582	30	NZ_CP022366	Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence	500020-500049	7	0.767
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	MH791411	UNVERIFIED: Escherichia phage Ecwhy_1, complete genome	335704-335733	7	0.767
NZ_CP043617_4	4.29\|2139014\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2139014-2139043	30	NC_022536	Rhizobium sp. IRBG74 plasmid IRBL74_p, complete sequence	13569-13598	7	0.767
NZ_CP043617_4	4.29\|2139014\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2139014-2139043	30	NZ_CP053858	Rhizobium pusense strain 76 plasmid pR76, complete sequence	18764-18793	7	0.767
NZ_CP043617_4	4.29\|2139014\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2139014-2139043	30	NZ_CP033024	Agrobacterium fabrum strain 1D132 plasmid pAt1D132a, complete sequence	13968-13997	7	0.767
NZ_CP043617_4	4.30\|2139080\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2139080-2139109	30	NZ_CP045339	Vibrio sp. THAF190c plasmid pTHAF190c_a, complete sequence	1644105-1644134	7	0.767
NZ_CP043617_4	4.33\|2139277\|29\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2139277-2139305	29	NZ_CP017217	Borreliella burgdorferi strain B331 plasmid B331_lp38, complete sequence	25902-25930	7	0.759
NZ_CP043617_4	4.33\|2139277\|29\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2139277-2139305	29	NC_017421	Borreliella burgdorferi N40 plasmid N40_lp38, complete sequence	27252-27280	7	0.759
NZ_CP043617_4	4.33\|2139277\|29\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2139277-2139305	29	NC_001856	Borreliella burgdorferi B31 plasmid lp38, complete sequence	26962-26990	7	0.759
NZ_CP043617_4	4.33\|2139277\|29\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2139277-2139305	29	NZ_CP019853	Borreliella burgdorferi plasmid lp38, complete sequence	26975-27003	7	0.759
NZ_CP043617_4	4.33\|2139277\|29\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2139277-2139305	29	NZ_CP019764	Borreliella burgdorferi strain B31_NRZ isolate B31 plasmid p_lp38, complete sequence	26968-26996	7	0.759
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	NZ_CP027419	Staphylococcus cohnii strain FDAARGOS_334 plasmid unnamed2, complete sequence	5384-5413	8	0.733
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	NZ_CP017461	Staphylococcus nepalensis strain JS1 plasmid pSNJS101, complete sequence	51955-51984	8	0.733
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	CP019598	Staphylococcus cohnii strain SNUDS-2 plasmid pSC-SNUDS-2-1, complete sequence	23146-23175	8	0.733
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	NZ_CP014171	Clostridium tyrobutyricum strain KCTC 5387 plasmid pCTK01, complete sequence	60480-60509	8	0.733
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	CP016281	Clostridium tyrobutyricum strain W428 plasmid pW428, complete sequence	39091-39120	8	0.733
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	NZ_KX274135	Staphylococcus arlettae strain SA-01 plasmid pSA-01, complete sequence	11500-11529	8	0.733
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	NZ_CP033734	Staphylococcus cohnii strain FDAARGOS_538 plasmid unnamed, complete sequence	30213-30242	8	0.733
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	NZ_CP017467	Staphylococcus nepalensis strain JS11 plasmid pSNJS1101, complete sequence	38547-38576	8	0.733
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	NZ_CP054578	Staphylococcus saprophyticus strain UTI-050 plasmid pUTI-050-3, complete sequence	6054-6083	8	0.733
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	CP031730	Stenotrophomonas rhizophila strain GA1 plasmid unnamed1, complete sequence	6168-6197	8	0.733
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	NZ_CP045225	Clostridioides difficile strain TW11 plasmid p_TW11, complete sequence	18138-18167	8	0.733
NZ_CP043617_4	4.9\|2137697\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137697-2137726	30	NZ_CP050315	Shewanella aestuarii strain PN3F2 plasmid pPN3F2_2, complete sequence	28473-28502	8	0.733
NZ_CP043617_4	4.13\|2137961\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137961-2137990	30	KJ019082	Synechococcus phage ACG-2014i isolate Syn7803US120, complete genome	118848-118877	8	0.733
NZ_CP043617_4	4.13\|2137961\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137961-2137990	30	NZ_CP015803	Borrelia mayonii strain MN14-1539 plasmid lp17	6593-6622	8	0.733
NZ_CP043617_4	4.13\|2137961\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137961-2137990	30	NZ_CP015788	Borrelia mayonii strain MN14-1420 plasmid lp17, complete sequence	6593-6622	8	0.733
NZ_CP043617_4	4.13\|2137961\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137961-2137990	30	AP013398	Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-U-MedDCM-OCT-S30-C38	3812-3841	8	0.733
NZ_CP043617_4	4.14\|2138027\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138027-2138056	30	KY554772	Lactococcus phage AM5, complete genome	43006-43035	8	0.733
NZ_CP043617_4	4.14\|2138027\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138027-2138056	30	NC_049856	Lactococcus phage AM4, complete genome	25051-25080	8	0.733
NZ_CP043617_4	4.14\|2138027\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138027-2138056	30	LN681542	Clostridium phage phiMMP03, complete genome	6409-6438	8	0.733
NZ_CP043617_4	4.14\|2138027\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138027-2138056	30	AY522333	Clostridium difficile phage phiC2 isolate 1.9 capsid protein gene, complete cds	907-936	8	0.733
NZ_CP043617_4	4.14\|2138027\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138027-2138056	30	HG531805	Clostridium phage CDMH1 complete genome	6655-6684	8	0.733
NZ_CP043617_4	4.14\|2138027\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138027-2138056	30	NC_009231	Clostridium phage phiC2, complete genome	6440-6469	8	0.733
NZ_CP043617_4	4.14\|2138027\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138027-2138056	30	LN681541	Clostridium phage phiMMP01, complete genome	6409-6438	8	0.733
NZ_CP043617_4	4.15\|2138093\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138093-2138122	30	MN693197	Marine virus AFVG_25M502, complete genome	5599-5628	8	0.733
NZ_CP043617_4	4.17\|2138225\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2138225-2138254	30	MG589384	Enterobacter phage phi63_307, complete genome	39017-39046	8	0.733
NZ_CP043617_4	4.17\|2138225\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2138225-2138254	30	MK759884	Salmonella phage vB_SenM_SB18, complete genome	55203-55232	8	0.733
NZ_CP043617_4	4.17\|2138225\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2138225-2138254	30	MK759884	Salmonella phage vB_SenM_SB18, complete genome	55501-55530	8	0.733
NZ_CP043617_4	4.17\|2138225\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2138225-2138254	30	NC_015292	Erwinia phage phiEa104, complete genome	55219-55248	8	0.733
NZ_CP043617_4	4.17\|2138225\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2138225-2138254	30	MH426725	Erwinia phage SunLIRen, complete genome	55219-55248	8	0.733
NZ_CP043617_4	4.17\|2138225\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2138225-2138254	30	FQ482083	Erwinia amylovora phage phiEa104 complete genome	55219-55248	8	0.733
NZ_CP043617_4	4.17\|2138225\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2138225-2138254	30	NC_011811	Erwinia phage phiEa21-4, complete genome	55233-55262	8	0.733
NZ_CP043617_4	4.17\|2138225\|30\|NZ_CP043617\|CRISPRCasFinder,CRT	2138225-2138254	30	MN604407	Salmonella phage ST-3, complete genome	28652-28681	8	0.733
NZ_CP043617_4	4.23\|2138619\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138619-2138648	30	NZ_CP024314	Rhizobium sp. NXC24 plasmid pRspNXC24c, complete sequence	1106496-1106525	8	0.733
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	NZ_CP007648	Lactobacillus salivarius strain JCM1046 plasmid pMP1046B, complete sequence	107151-107180	8	0.733
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	NZ_CP014283	Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence	597277-597306	8	0.733
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	NZ_CP022446	Bacillus cereus C1L plasmid pC1L1, complete sequence	105758-105787	8	0.733
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	NZ_CP032614	Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence	286461-286490	8	0.733
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	MN694545	Marine virus AFVG_250M894, complete genome	37903-37932	8	0.733
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	NZ_CP029455	Bacillus cereus strain FORC087 plasmid pFORC087.1, complete sequence	343218-343247	8	0.733
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	NZ_CP050184	Bacillus thuringiensis strain HER1410 plasmid pLUSID1, complete sequence	123157-123186	8	0.733
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	NC_014533	Gloeothece verrucosa PCC 7822 plasmid Cy782201, complete sequence	450363-450392	9	0.7
NZ_CP043617_4	4.24\|2138685\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2138685-2138714	30	KJ608188	Enterococcus phage EFC-1, complete genome	4104-4133	9	0.7
NZ_CP043617_4	4.30\|2139080\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2139080-2139109	30	NZ_CP030933	Enterococcus gilvus strain CR1 plasmid pCR1A, complete sequence	776569-776598	9	0.7
NZ_CP043617_4	4.32\|2139211\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2139211-2139240	30	NZ_CP045296	Paenibacillus cellulositrophicus strain KACC 16577 plasmid unnamed1, complete sequence	121600-121629	9	0.7
NZ_CP043617_4	4.34\|2139342\|30\|NZ_CP043617\|CRT	2139342-2139371	30	NZ_CP045296	Paenibacillus cellulositrophicus strain KACC 16577 plasmid unnamed1, complete sequence	121600-121629	9	0.7
NZ_CP043617_4	4.7\|2137565\|30\|NZ_CP043617\|CRISPRCasFinder,CRT,PILER-CR	2137565-2137594	30	NZ_CP031220	Arcobacter mytili LMG 24559 plasmid pAMYT, complete sequence	87266-87295	15	0.5

1. spacer 4.2|2137391|26|NZ_CP043617|PILER-CR matches to NZ_CP048772 (Campylobacter jejuni strain ZS007 plasmid pCJ145K, complete sequence) position: , mismatch: 3, identity: 0.885

gtgaaagtttagagtattattctaaa	CRISPR spacer
atggaagtttagagttttattctaaa	Protospacer
.**.*********** **********

2. spacer 4.2|2137391|26|NZ_CP043617|PILER-CR matches to NZ_MK275621 (Clostridium perfringens strain JXJA17 plasmid p3, complete sequence) position: , mismatch: 3, identity: 0.885

gtgaaag---tttagagtattattctaaa	CRISPR spacer
---aaagttttttagagtattattctaaa	Protospacer
   ****   *******************

3. spacer 4.2|2137391|26|NZ_CP043617|PILER-CR matches to NZ_CP014857 (Lysinibacillus sphaericus III(3)7 plasmid, complete sequence) position: , mismatch: 4, identity: 0.846

gtgaaagtttagagtattattctaaa	CRISPR spacer
tttaaagtttaaagtattattcttaa	Protospacer
 * ********.*********** **

4. spacer 4.2|2137391|26|NZ_CP043617|PILER-CR matches to NZ_CP014644 (Lysinibacillus sphaericus strain OT4b.25 plasmid unnamed, complete sequence) position: , mismatch: 4, identity: 0.846

gtgaaagtttagagtattattctaaa	CRISPR spacer
tttaaagtttaaagtattattcttaa	Protospacer
 * ********.*********** **

5. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to AP013392 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C6A-MedDCM-OCT-S43-C64) position: , mismatch: 5, identity: 0.833

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
agcacaattaggaaatgaaattaccaaagc	Protospacer
**   ******************* ****

6. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to AP013391 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C6A-MedDCM-OCT-S33-C54) position: , mismatch: 5, identity: 0.833

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
agcacaattaggaaatgaaattaccaaagc	Protospacer
**   ******************* ****

7. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to AP013390 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C6-MedDCM-OCT-S27-C41) position: , mismatch: 5, identity: 0.833

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
agcacaattaggaaatgaaattaccaaagc	Protospacer
**   ******************* ****

8. spacer 4.4|2137367|30|NZ_CP043617|CRISPRCasFinder,CRT matches to NZ_CP014644 (Lysinibacillus sphaericus strain OT4b.25 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.8

caaagtgaaagtttagagtattattctaaa	CRISPR spacer
aaagtttaaagtttaaagtattattcttaa	Protospacer
 **. * ********.*********** **

9. spacer 4.4|2137367|30|NZ_CP043617|CRISPRCasFinder,CRT matches to NZ_CP014857 (Lysinibacillus sphaericus III(3)7 plasmid, complete sequence) position: , mismatch: 6, identity: 0.8

caaagtgaaagtttagagtattattctaaa	CRISPR spacer
aaagtttaaagtttaaagtattattcttaa	Protospacer
 **. * ********.*********** **

10. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to MN694255 (Marine virus AFVG_250M362, complete genome) position: , mismatch: 6, identity: 0.8

-agtatgtttttatataaatgatttagaaca	CRISPR spacer
tggta-gtttttatatatatgattttgaaac	Protospacer
 .*** *********** ******* ***

11. spacer 4.14|2138027|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP028882 (Borreliella bavariensis PBi plasmid lp28-3, complete sequence) position: , mismatch: 6, identity: 0.8

atgacaggtgtatttatagcacttggaaca	CRISPR spacer
aaaacaagtgtatttatagcacttataaaa	Protospacer
* .***.*****************. ** *

12. spacer 4.17|2138225|30|NZ_CP043617|CRISPRCasFinder,CRT matches to AP013543 (Uncultured phage_MedDCM-OCT-S30-C28 DNA, complete genome, group G8, isolate: uvMED-CGR-U-MedDCM-OCT-S30-C28) position: , mismatch: 6, identity: 0.8

atagcttac-aaatggtaaaagcagaatcag	CRISPR spacer
-tttcttgtaaaatggtaaaagcagaaacag	Protospacer
 *  ***.. ***************** ***

13. spacer 4.18|2138291|29|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to KY653124 (Staphylococcus phage IME1367_01, complete genome) position: , mismatch: 6, identity: 0.793

aaaggtgtaataaatgaatctaaaaccaa	CRISPR spacer
aaagatgtaatagatgaatctaaaatacc	Protospacer
****.*******.************.

14. spacer 4.18|2138291|29|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to MK554696 (Fusobacterium phage Fnu1, complete genome) position: , mismatch: 6, identity: 0.793

aaaggtgtaataaatgaatctaaaaccaa	CRISPR spacer
gtagatgtaataaatgaatataaaaataa	Protospacer
. **.************** ***** .**

15. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NC_022778 (Clostridium tetani 12124569 plasmid p12124569, complete sequence) position: , mismatch: 6, identity: 0.8

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
aataaaatcaggaattgaaattacaaaaca	Protospacer
*.  ****.***** ************* *

16. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to KP836356 (Marinitoga camini virus 2, complete genome) position: , mismatch: 6, identity: 0.8

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
agataaattaggaaatgaaataacttataa	Protospacer
***.***************** **  * .*

17. spacer 4.29|2139014|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NC_008382 (Rhizobium leguminosarum bv. viciae 3841 plasmid pRL7, complete sequence) position: , mismatch: 6, identity: 0.8

aaaagtgttttatgatctaaatgcaccggc	CRISPR spacer
aagcgtgttttatgatccaaatgcagcccc	Protospacer
**. *************.******* *  *

18. spacer 4.31|2139146|29|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_AP017296 (Nostoc sp. NIES-3756 plasmid pNOS3756_1, complete sequence) position: , mismatch: 6, identity: 0.793

cgcgtgggtacaaaaccctaatttaattt	CRISPR spacer
gggagggttacaaaaccctaacttaattt	Protospacer
 * . ** *************.*******

19. spacer 4.4|2137367|30|NZ_CP043617|CRISPRCasFinder,CRT matches to NZ_CP048772 (Campylobacter jejuni strain ZS007 plasmid pCJ145K, complete sequence) position: , mismatch: 7, identity: 0.767

caaagtgaaagtttagagtattattctaaa	CRISPR spacer
atttatggaagtttagagttttattctaaa	Protospacer
    .**.*********** **********

20. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to MN693159 (Marine virus AFVG_25M303, complete genome) position: , mismatch: 7, identity: 0.767

agtatgtttttatataaatgatttagaaca	CRISPR spacer
tgttagtttttatgtaaatggtttagaagt	Protospacer
 **  ********.******.*******

21. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NC_014839 (Pantoea sp. At-9b plasmid pPAT9B02, complete sequence) position: , mismatch: 7, identity: 0.767

agtatgtttttatataaatgatttagaaca	CRISPR spacer
tgtatgtttttatataaattcttttcaccg	Protospacer
 ******************  ***  * *.

22. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP009368 (Bacillus cereus strain FM1 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

agtatgtttttatataaatgatttagaaca	CRISPR spacer
tgtgaaattttatataaaaaatttagaaca	Protospacer
 **. . *********** .**********

23. spacer 4.13|2137961|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to AP014137 (Uncultured Mediterranean phage uvMED isolate uvMED-GF-C47-MedDCM-OCT-S35-C41, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 7, identity: 0.767

tgttatctcatcatattagaaaaataaact	CRISPR spacer
ggttatctcctcaaattagaaaaatttgca	Protospacer
 ******** *** ***********  .*

24. spacer 4.16|2138159|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP049297 (Bacillus megaterium strain S188 plasmid pS188, complete sequence) position: , mismatch: 7, identity: 0.767

actaattctcaattgaaattccaaaatgag	CRISPR spacer
gaaaattctcaattgaatttcgaaaagaag	Protospacer
.  ************** *** **** .**

25. spacer 4.16|2138159|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP045274 (Bacillus megaterium strain FDU301 plasmid pFDU301B, complete sequence) position: , mismatch: 7, identity: 0.767

actaattctcaattgaaattccaaaatgag	CRISPR spacer
gaaaattctcaattgaatttcgaaaagaag	Protospacer
.  ************** *** **** .**

26. spacer 4.17|2138225|30|NZ_CP043617|CRISPRCasFinder,CRT matches to MK250029 (Prevotella phage Lak-C1, complete genome) position: , mismatch: 7, identity: 0.767

atagcttacaaatggtaaaagcagaatcag	CRISPR spacer
ttcatttacaaatgaaaaaagcagaatcat	Protospacer
 * ..*********. *************

27. spacer 4.17|2138225|30|NZ_CP043617|CRISPRCasFinder,CRT matches to MK250016 (Prevotella phage Lak-A1, complete genome) position: , mismatch: 7, identity: 0.767

atagcttacaaatggtaaaagcagaatcag	CRISPR spacer
ttcatttacaaatgaaaaaagcagaatcat	Protospacer
 * ..*********. *************

28. spacer 4.17|2138225|30|NZ_CP043617|CRISPRCasFinder,CRT matches to MK250019 (Prevotella phage Lak-A2, complete genome) position: , mismatch: 7, identity: 0.767

atagcttacaaatggtaaaagcagaatcag	CRISPR spacer
ttcatttacaaatgaaaaaagcagaatcat	Protospacer
 * ..*********. *************

29. spacer 4.18|2138291|29|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to MN855613 (Siphoviridae sp. isolate 60, complete genome) position: , mismatch: 7, identity: 0.759

aaaggtgtaataaatgaatctaaaaccaa	CRISPR spacer
gaaggtgtaaaaaatgaaactaaataaga	Protospacer
.********* ******* *****   .*

30. spacer 4.19|2138356|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015602 (Pseudomonas antarctica strain PAMC 27494 plasmid pP27494_2, complete sequence) position: , mismatch: 7, identity: 0.767

cataactttgtcggaggtgttacgaaaagt	CRISPR spacer
cataacttcgtcgtaggtgttactagccat	Protospacer
********.**** ********* *.  .*

31. spacer 4.22|2138553|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022366 (Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence) position: , mismatch: 7, identity: 0.767

tagacttttcgccatcaaaacctttacgtt-	CRISPR spacer
cggccttttcgccatcaagaccttt-cgcca	Protospacer
..* **************.****** **..

32. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to MH791411 (UNVERIFIED: Escherichia phage Ecwhy_1, complete genome) position: , mismatch: 7, identity: 0.767

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
tgataaattaggaaacgaaattacttatta	Protospacer
 **.***********.********  *  *

33. spacer 4.29|2139014|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NC_022536 (Rhizobium sp. IRBG74 plasmid IRBL74_p, complete sequence) position: , mismatch: 7, identity: 0.767

aaaagtgttttatgatctaaatgcaccggc	CRISPR spacer
aagcgtgttttatgacctaaatgcaggccc	Protospacer
**. ***********.*********    *

34. spacer 4.29|2139014|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP053858 (Rhizobium pusense strain 76 plasmid pR76, complete sequence) position: , mismatch: 7, identity: 0.767

aaaagtgttttatgatctaaatgcaccggc	CRISPR spacer
aagcgtgttttatgacctaaatgcaggccc	Protospacer
**. ***********.*********    *

35. spacer 4.29|2139014|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP033024 (Agrobacterium fabrum strain 1D132 plasmid pAt1D132a, complete sequence) position: , mismatch: 7, identity: 0.767

aaaagtgttttatgatctaaatgcaccggc	CRISPR spacer
aagtgtgttttatgacctaaatgcagccct	Protospacer
**. ***********.********* *  .

36. spacer 4.30|2139080|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP045339 (Vibrio sp. THAF190c plasmid pTHAF190c_a, complete sequence) position: , mismatch: 7, identity: 0.767

-atgtttgttggcaaagagcttttaactaaa	CRISPR spacer
catg-atgttggcaaagggcttttaacgccc	Protospacer
 ***  ***********.*********

37. spacer 4.33|2139277|29|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP017217 (Borreliella burgdorferi strain B331 plasmid B331_lp38, complete sequence) position: , mismatch: 7, identity: 0.759

cgcgtgggtgcaaaaccctaatttaattt	CRISPR spacer
gtttttggtgtaaaaccctaattttattt	Protospacer
  . * ****.************* ****

38. spacer 4.33|2139277|29|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NC_017421 (Borreliella burgdorferi N40 plasmid N40_lp38, complete sequence) position: , mismatch: 7, identity: 0.759

cgcgtgggtgcaaaaccctaatttaattt	CRISPR spacer
gtttttggtgtaaaaccctaattttattt	Protospacer
  . * ****.************* ****

39. spacer 4.33|2139277|29|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NC_001856 (Borreliella burgdorferi B31 plasmid lp38, complete sequence) position: , mismatch: 7, identity: 0.759

cgcgtgggtgcaaaaccctaatttaattt	CRISPR spacer
gtttttggtgtaaaaccctaattttattt	Protospacer
  . * ****.************* ****

40. spacer 4.33|2139277|29|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP019853 (Borreliella burgdorferi plasmid lp38, complete sequence) position: , mismatch: 7, identity: 0.759

cgcgtgggtgcaaaaccctaatttaattt	CRISPR spacer
gtttttggtgtaaaaccctaattttattt	Protospacer
  . * ****.************* ****

41. spacer 4.33|2139277|29|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP019764 (Borreliella burgdorferi strain B31_NRZ isolate B31 plasmid p_lp38, complete sequence) position: , mismatch: 7, identity: 0.759

cgcgtgggtgcaaaaccctaatttaattt	CRISPR spacer
gtttttggtgtaaaaccctaattttattt	Protospacer
  . * ****.************* ****

42. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP027419 (Staphylococcus cohnii strain FDAARGOS_334 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.733

agtatgtttttatataaatgatttagaaca	CRISPR spacer
ttaatgtttttatataactgatttagtttc	Protospacer
   ************** ********  .

43. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP017461 (Staphylococcus nepalensis strain JS1 plasmid pSNJS101, complete sequence) position: , mismatch: 8, identity: 0.733

agtatgtttttatataaatgatttagaaca	CRISPR spacer
ttaatgtttttatataactgatttagtttc	Protospacer
   ************** ********  .

44. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to CP019598 (Staphylococcus cohnii strain SNUDS-2 plasmid pSC-SNUDS-2-1, complete sequence) position: , mismatch: 8, identity: 0.733

agtatgtttttatataaatgatttagaaca	CRISPR spacer
ttaatgtttttatataactgatttagtttc	Protospacer
   ************** ********  .

45. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP014171 (Clostridium tyrobutyricum strain KCTC 5387 plasmid pCTK01, complete sequence) position: , mismatch: 8, identity: 0.733

agtatgtttttatataaatgatt------tagaaca	CRISPR spacer
tatatgtttttatataaatgattgcctcat------	Protospacer
 .*********************      *

46. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to CP016281 (Clostridium tyrobutyricum strain W428 plasmid pW428, complete sequence) position: , mismatch: 8, identity: 0.733

agtatgtttttatataaatgatt------tagaaca	CRISPR spacer
tatatgtttttatataaatgattgcctcat------	Protospacer
 .*********************      *

47. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_KX274135 (Staphylococcus arlettae strain SA-01 plasmid pSA-01, complete sequence) position: , mismatch: 8, identity: 0.733

agtatgtttttatataaatgatttagaaca	CRISPR spacer
ttaatgtttttatataactgatttagtttc	Protospacer
   ************** ********  .

48. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP033734 (Staphylococcus cohnii strain FDAARGOS_538 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.733

agtatgtttttatataaatgatttagaaca	CRISPR spacer
ttaatgtttttatataactgatttagtttc	Protospacer
   ************** ********  .

49. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP017467 (Staphylococcus nepalensis strain JS11 plasmid pSNJS1101, complete sequence) position: , mismatch: 8, identity: 0.733

agtatgtttttatataaatgatttagaaca	CRISPR spacer
ttaatgtttttatataactgatttagtttc	Protospacer
   ************** ********  .

50. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP054578 (Staphylococcus saprophyticus strain UTI-050 plasmid pUTI-050-3, complete sequence) position: , mismatch: 8, identity: 0.733

agtatgtttttatataaatgatttagaaca	CRISPR spacer
ttaatgtttttatataactgatttagtttc	Protospacer
   ************** ********  .

51. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to CP031730 (Stenotrophomonas rhizophila strain GA1 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.733

agtatgtttttatataaatgatttagaaca	CRISPR spacer
tcgttgtttttttatagatgatttagaagt	Protospacer
    ******* ****.***********

52. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP045225 (Clostridioides difficile strain TW11 plasmid p_TW11, complete sequence) position: , mismatch: 8, identity: 0.733

agtatgtttttatataaatgatttagaaca	CRISPR spacer
tttatatttttatataaatgattctttaaa	Protospacer
  ***.*****************.   * *

53. spacer 4.9|2137697|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050315 (Shewanella aestuarii strain PN3F2 plasmid pPN3F2_2, complete sequence) position: , mismatch: 8, identity: 0.733

ttttcgcaagaggacaattcaaccaccaga	CRISPR spacer
ttttcgcaagaggaccatttaacatgtcca	Protospacer
*************** ***.***   .  *

54. spacer 4.13|2137961|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to KJ019082 (Synechococcus phage ACG-2014i isolate Syn7803US120, complete genome) position: , mismatch: 8, identity: 0.733

tgttatctcatcatattagaaaaataaact	CRISPR spacer
ggttatctcctcaaattagaaaaatttgaa	Protospacer
 ******** *** ***********  .

55. spacer 4.13|2137961|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015803 (Borrelia mayonii strain MN14-1539 plasmid lp17) position: , mismatch: 8, identity: 0.733

tgttatctcatcatattagaaaaataaact	CRISPR spacer
aaatgcctcaacatattagaaaaagaaaca	Protospacer
 . *..**** ************* ****

56. spacer 4.13|2137961|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015788 (Borrelia mayonii strain MN14-1420 plasmid lp17, complete sequence) position: , mismatch: 8, identity: 0.733

tgttatctcatcatattagaaaaataaact	CRISPR spacer
aaatgcctcaacatattagaaaaagaaaca	Protospacer
 . *..**** ************* ****

57. spacer 4.13|2137961|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to AP013398 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-U-MedDCM-OCT-S30-C38) position: , mismatch: 8, identity: 0.733

tgttatctcatcatattagaaaaataaact	CRISPR spacer
agttatctgagcatattagaaaaaactata	Protospacer
 ******* * *************   *.

58. spacer 4.14|2138027|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to KY554772 (Lactococcus phage AM5, complete genome) position: , mismatch: 8, identity: 0.733

atgacaggtgtatttatagcacttggaaca	CRISPR spacer
ccatcaagtgtatttatagcactttgaaat	Protospacer
 .. **.***************** ***

59. spacer 4.14|2138027|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NC_049856 (Lactococcus phage AM4, complete genome) position: , mismatch: 8, identity: 0.733

atgacaggtgtatttatagcacttggaaca	CRISPR spacer
ccatcaagtgtatttatagcactttgaaat	Protospacer
 .. **.***************** ***

60. spacer 4.14|2138027|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to LN681542 (Clostridium phage phiMMP03, complete genome) position: , mismatch: 8, identity: 0.733

atgacaggtgtatttatagcacttggaaca	CRISPR spacer
gaaacaggtgtaattattgcacttgggtga	Protospacer
. .********* **** ********.  *

61. spacer 4.14|2138027|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to AY522333 (Clostridium difficile phage phiC2 isolate 1.9 capsid protein gene, complete cds) position: , mismatch: 8, identity: 0.733

atgacaggtgtatttatagcacttggaaca	CRISPR spacer
gaaacaggtgtaattattgcacttgggtga	Protospacer
. .********* **** ********.  *

62. spacer 4.14|2138027|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to HG531805 (Clostridium phage CDMH1 complete genome) position: , mismatch: 8, identity: 0.733

atgacaggtgtatttatagcacttggaaca	CRISPR spacer
gaaacaggtgtaattattgcacttgggtga	Protospacer
. .********* **** ********.  *

63. spacer 4.14|2138027|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NC_009231 (Clostridium phage phiC2, complete genome) position: , mismatch: 8, identity: 0.733

atgacaggtgtatttatagcacttggaaca	CRISPR spacer
gaaacaggtgtaattattgcacttgggtga	Protospacer
. .********* **** ********.  *

64. spacer 4.14|2138027|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to LN681541 (Clostridium phage phiMMP01, complete genome) position: , mismatch: 8, identity: 0.733

atgacaggtgtatttatagcacttggaaca	CRISPR spacer
gaaacaggtgtaattattgcacttgggtga	Protospacer
. .********* **** ********.  *

65. spacer 4.15|2138093|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to MN693197 (Marine virus AFVG_25M502, complete genome) position: , mismatch: 8, identity: 0.733

tacctaaaagagctggacgcatacagcttg	CRISPR spacer
tagttaaaagagatggacgcatacaagaat	Protospacer
** .******** ************.

66. spacer 4.17|2138225|30|NZ_CP043617|CRISPRCasFinder,CRT matches to MG589384 (Enterobacter phage phi63_307, complete genome) position: , mismatch: 8, identity: 0.733

atagcttacaaatggtaaaagcagaatcag	CRISPR spacer
aaggcttacaaatgggaaaagctgaagtct	Protospacer
* .************ ****** *** .

67. spacer 4.17|2138225|30|NZ_CP043617|CRISPRCasFinder,CRT matches to MK759884 (Salmonella phage vB_SenM_SB18, complete genome) position: , mismatch: 8, identity: 0.733

atagcttacaaatggtaaaagcagaatcag	CRISPR spacer
aaggcttacaaatgggaaaagctgaagtct	Protospacer
* .************ ****** *** .

68. spacer 4.17|2138225|30|NZ_CP043617|CRISPRCasFinder,CRT matches to MK759884 (Salmonella phage vB_SenM_SB18, complete genome) position: , mismatch: 8, identity: 0.733

atagcttacaaatggtaaaagcagaatcag	CRISPR spacer
aaggcttacaaatgggaaaagctgaagtct	Protospacer
* .************ ****** *** .

69. spacer 4.17|2138225|30|NZ_CP043617|CRISPRCasFinder,CRT matches to NC_015292 (Erwinia phage phiEa104, complete genome) position: , mismatch: 8, identity: 0.733

atagcttacaaatggtaaaagcagaatcag	CRISPR spacer
aaggcttacaaatgggaaaagctgaagtct	Protospacer
* .************ ****** *** .

70. spacer 4.17|2138225|30|NZ_CP043617|CRISPRCasFinder,CRT matches to MH426725 (Erwinia phage SunLIRen, complete genome) position: , mismatch: 8, identity: 0.733

atagcttacaaatggtaaaagcagaatcag	CRISPR spacer
aaggcttacaaatgggaaaagctgaagtct	Protospacer
* .************ ****** *** .

71. spacer 4.17|2138225|30|NZ_CP043617|CRISPRCasFinder,CRT matches to FQ482083 (Erwinia amylovora phage phiEa104 complete genome) position: , mismatch: 8, identity: 0.733

atagcttacaaatggtaaaagcagaatcag	CRISPR spacer
aaggcttacaaatgggaaaagctgaagtct	Protospacer
* .************ ****** *** .

72. spacer 4.17|2138225|30|NZ_CP043617|CRISPRCasFinder,CRT matches to NC_011811 (Erwinia phage phiEa21-4, complete genome) position: , mismatch: 8, identity: 0.733

atagcttacaaatggtaaaagcagaatcag	CRISPR spacer
aaggcttacaaatgggaaaagctgaagtct	Protospacer
* .************ ****** *** .

73. spacer 4.17|2138225|30|NZ_CP043617|CRISPRCasFinder,CRT matches to MN604407 (Salmonella phage ST-3, complete genome) position: , mismatch: 8, identity: 0.733

atagcttacaaatggtaaaagcagaatcag	CRISPR spacer
aaggcttacaaatgggaaaagctgaagtct	Protospacer
* .************ ****** *** .

74. spacer 4.23|2138619|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP024314 (Rhizobium sp. NXC24 plasmid pRspNXC24c, complete sequence) position: , mismatch: 8, identity: 0.733

tgtcctactgatatattgatactcattttt	CRISPR spacer
tgtcctattgatatattgatacattagtgc	Protospacer
*******.************** .   * .

75. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP007648 (Lactobacillus salivarius strain JCM1046 plasmid pMP1046B, complete sequence) position: , mismatch: 8, identity: 0.733

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
agaaaaattaggaaatgatattaaagctac	Protospacer
*** ************** **** *.  .

76. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP014283 (Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence) position: , mismatch: 8, identity: 0.733

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
ctaatgtttacgaaatgaaattaaaaaaga	Protospacer
  *  . *** ************ ******

77. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022446 (Bacillus cereus C1L plasmid pC1L1, complete sequence) position: , mismatch: 8, identity: 0.733

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
ctaatgtttacgaaatgaaattaaaaaaga	Protospacer
  *  . *** ************ ******

78. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032614 (Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence) position: , mismatch: 8, identity: 0.733

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
ctaatgtttacgaaatgaaattaaaaaaga	Protospacer
  *  . *** ************ ******

79. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to MN694545 (Marine virus AFVG_250M894, complete genome) position: , mismatch: 8, identity: 0.733

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
agataaattaggaaatgaaatggctggaag	Protospacer
***.***************** .* ..*..

80. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP029455 (Bacillus cereus strain FORC087 plasmid pFORC087.1, complete sequence) position: , mismatch: 8, identity: 0.733

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
ttaatgtttacgaaatgaaattaaaaaaga	Protospacer
  *  . *** ************ ******

81. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050184 (Bacillus thuringiensis strain HER1410 plasmid pLUSID1, complete sequence) position: , mismatch: 8, identity: 0.733

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
ctaatgtttacgaaatgaaattaaaaaaga	Protospacer
  *  . *** ************ ******

82. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NC_014533 (Gloeothece verrucosa PCC 7822 plasmid Cy782201, complete sequence) position: , mismatch: 9, identity: 0.7

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
agaaaaattagaaaatgaaattaattgttt	Protospacer
*** *******.***********   .

83. spacer 4.24|2138685|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to KJ608188 (Enterococcus phage EFC-1, complete genome) position: , mismatch: 9, identity: 0.7

agacaaattaggaaatgaaattacaaaaga	CRISPR spacer
ttttaaatcaggtaatgaaattacaaattt	Protospacer
   .****.*** **************

84. spacer 4.30|2139080|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP030933 (Enterococcus gilvus strain CR1 plasmid pCR1A, complete sequence) position: , mismatch: 9, identity: 0.7

atgtttgttggcaaagagcttttaactaaa	CRISPR spacer
tgttttgttggcaaagagctcttagttttc	Protospacer
   *****************.***..*

85. spacer 4.32|2139211|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP045296 (Paenibacillus cellulositrophicus strain KACC 16577 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.7

atgagtagagttacttattattcattagat	CRISPR spacer
caatttatagttactaattattcattagta	Protospacer
  .  ** ******* ************

86. spacer 4.34|2139342|30|NZ_CP043617|CRT matches to NZ_CP045296 (Paenibacillus cellulositrophicus strain KACC 16577 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.7

atgagtagagttacttattattcattagat	CRISPR spacer
caatttatagttactaattattcattagta	Protospacer
  .  ** ******* ************

87. spacer 4.7|2137565|30|NZ_CP043617|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP031220 (Arcobacter mytili LMG 24559 plasmid pAMYT, complete sequence) position: , mismatch: 15, identity: 0.5

agtatgtttttatataaatgatttagaaca---------	CRISPR spacer
---------gtatagtaatgatttatataaaaatatact	Protospacer
          ****  ********* *  *

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

766032 : 844327

Indivirus(25.0%)

protease,plate

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_152306855.1\|766032_767268_-\|protease	ATP-dependent Clp protease ATP-binding subunit ClpX	G3M9Z9	Bacillus_virus	4.9e-116	52.1
WP_152306856.1\|767264_768053_-	acyl-ACP--UDP-N-acetylglucosamine O-acyltransferase	NA	NA	NA	NA
WP_152306857.1\|768064_768511_-	3-hydroxyacyl-ACP dehydratase FabZ	NA	NA	NA	NA
WP_152306858.1\|768570_769665_-	diacylglucosamine hydrolase like protein	NA	NA	NA	NA
WP_152306859.1\|769749_770253_-	peptidylprolyl isomerase	A0A1V0SCU1	Indivirus	1.6e-17	43.1
WP_152308377.1\|770396_771611_+	sensor histidine kinase	Q6XLV6	Feldmannia_irregularis_virus	5.4e-06	25.8
WP_152306860.1\|771612_772269_+	response regulator	NA	NA	NA	NA
WP_152306861.1\|772356_774036_+	HAMP domain-containing protein	NA	NA	NA	NA
WP_152306862.1\|774203_775571_+	outer membrane porin, OprD family	NA	NA	NA	NA
WP_152306863.1\|775679_775994_+	DUF485 domain-containing protein	NA	NA	NA	NA
WP_152306864.1\|775995_777663_+	sodium/solute symporter	NA	NA	NA	NA
WP_152306865.1\|777716_779522_+	CBS domain-containing protein	NA	NA	NA	NA
WP_152306866.1\|779521_780151_+	3'-5' exonuclease	NA	NA	NA	NA
WP_152306867.1\|780140_782096_+	acetate--CoA ligase	A0A2H4PQU7	Staphylococcus_phage	6.5e-78	36.7
WP_152306868.1\|782164_782848_+	orotidine-5'-phosphate decarboxylase	NA	NA	NA	NA
WP_152306869.1\|783075_783324_-	hypothetical protein	NA	NA	NA	NA
WP_152306870.1\|783640_783928_-	hypothetical protein	NA	NA	NA	NA
WP_152306871.1\|783928_784711_-	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_152306872.1\|784759_785548_-	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_152306873.1\|785551_789505_-	hypothetical protein	NA	NA	NA	NA
WP_152306874.1\|789638_791132_+	type VI secretion system protein TssA	NA	NA	NA	NA
WP_152306875.1\|791143_791626_+	type VI secretion system contractile sheath small subunit	NA	NA	NA	NA
WP_152306876.1\|791635_793111_+	type VI secretion system contractile sheath large subunit	NA	NA	NA	NA
WP_152306877.1\|793110_793527_+\|plate	type VI secretion system baseplate subunit TssE	NA	NA	NA	NA
WP_152306878.1\|793516_795292_+\|plate	type VI secretion system baseplate subunit TssF	NA	NA	NA	NA
WP_152308378.1\|795295_796288_+\|plate	type VI secretion system baseplate subunit TssG	NA	NA	NA	NA
WP_152306879.1\|796290_798852_+	type VI secretion system ATPase TssH	K4FB40	Cronobacter_phage	4.6e-100	33.5
WP_152306880.1\|798995_800204_+	type VI secretion system-associated FHA domain protein TagH	NA	NA	NA	NA
WP_152306881.1\|800216_800654_+	type VI secretion system lipoprotein TssJ	NA	NA	NA	NA
WP_152306882.1\|800656_801988_+\|plate	type VI secretion system baseplate subunit TssK	NA	NA	NA	NA
WP_152306883.1\|801998_802889_+	DotU family type IV/VI secretion system protein	NA	NA	NA	NA
WP_152306884.1\|802881_806352_+	type VI secretion system membrane subunit TssM	NA	NA	NA	NA
WP_152306885.1\|806351_807032_+	SpoIIE family protein phosphatase	NA	NA	NA	NA
WP_152306886.1\|807019_807886_+	protein kinase	A0A1V0SKK4	Klosneuvirus	2.2e-14	27.4
WP_152306887.1\|807991_808516_+	type VI secretion system tube protein Hcp	NA	NA	NA	NA
WP_152306888.1\|808605_811530_+	type VI secretion system tip protein VgrG	NA	NA	NA	NA
WP_152306889.1\|811516_812686_+	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_152306890.1\|812675_814913_+	hypothetical protein	NA	NA	NA	NA
WP_152306891.1\|814915_815224_+	hypothetical protein	NA	NA	NA	NA
WP_152306892.1\|815273_816383_+	hypothetical protein	NA	NA	NA	NA
WP_152306893.1\|816390_816855_-	hypothetical protein	NA	NA	NA	NA
WP_152306894.1\|816914_818033_-	hypothetical protein	NA	NA	NA	NA
WP_152306895.1\|818176_823582_+	DUF4114 domain-containing protein	NA	NA	NA	NA
WP_152306896.1\|823600_824206_-	DNA-binding response regulator	NA	NA	NA	NA
WP_152306897.1\|824210_825551_-	HlyD family type I secretion periplasmic adaptor subunit	NA	NA	NA	NA
WP_152306898.1\|825534_827709_-	type I secretion system permease/ATPase	F2Y2R6	Organic_Lake_phycodnavirus	1.1e-20	34.1
WP_152306899.1\|827727_829590_-	TolC family outer membrane protein	NA	NA	NA	NA
WP_152306900.1\|829606_830383_-	OmpA family protein	NA	NA	NA	NA
WP_152306901.1\|830576_833606_+	DNA mismatch repair protein	A0A1V0SDQ0	Indivirus	6.6e-146	32.2
WP_152308379.1\|833602_834424_-	hypothetical protein	NA	NA	NA	NA
WP_152306902.1\|835230_836328_+	succinyl-diaminopimelate desuccinylase	NA	NA	NA	NA
WP_152306903.1\|836329_836758_+	DUF255 domain-containing protein	NA	NA	NA	NA
WP_152306904.1\|836754_837132_+	deaminase	NA	NA	NA	NA
WP_152306905.1\|837141_837729_+	TetR family transcriptional regulator	NA	NA	NA	NA
WP_152306906.1\|837731_838610_+	hydrogenase	NA	NA	NA	NA
WP_152306907.1\|838602_839862_+	hydrogenase	NA	NA	NA	NA
WP_152306908.1\|839987_841226_+	hydrogenase small subunit	NA	NA	NA	NA
WP_152306909.1\|841225_842974_+	hydrogenase 2 large subunit	NA	NA	NA	NA
WP_152306910.1\|842984_843686_+	Ni/Fe hydrogenase	NA	NA	NA	NA
WP_152306911.1\|843760_844327_+\|protease	hydrogenase maturation protease	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_CP043617

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CRISPR-Cas detection and classification

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Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

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Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection