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_CP022743	Mucilaginibacter xinganensis strain BJC16-A31 chromosome, complete genome	3 crisprs	cas3,DEDDh,csa3,WYL	0	0	0	0

Cas Category Instructions

Results visualization

1. NZ_CP022743

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP022743_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022743_1

865270-865385

Orphan

Consensus_repeat	Method
CTGTTCCGTTCGATATTTGTGCCGAACATGCTGAAACA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP022743_1

>merge|NZ_CP022743|1|865270-865385|CRISPRCasFinder
CTGTTCCGTTCGATATTTGTGCCGAACATGCTGAAACAAATGTGAAACAGCAGCTGATTTATTTTAAATTCCAATATCCTGTTCCGTTCGCTATTTGTGCCGAACATGCTGAAACA

>NZ_CP022743|1|1|865270-865385|CRISPRCasFinder
CTGTTCCGTTCGATATTTGTGCCGAACATGCTGAAACA	AATGTGAAACAGCAGCTGATTTATTTTAAATTCCAATATC
CTGTTCCGTTCGCTATTTGTGCCGAACATGCTGAAACA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022743.1\|WP_094569258.1\|861059_861695_+\|DNA-3-methyladenine-glycosylase-2-family-protein	unknown	unknown	gnl\|CDD\|223200
NZ_CP022743.1\|WP_157740584.1\|861705_862257_+\|sugar-O-acetyltransferase	unknown	unknown	gnl\|CDD\|100047
NZ_CP022743.1\|WP_094569255.1\|856856_857351_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP022743.1\|WP_094569265.1\|869143_870052_+\|cyanophycinase	unknown	unknown	gnl\|CDD\|131124
NZ_CP022743.1\|WP_157740588.1\|873145_873763_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022743.1\|WP_094569263.1\|865400_866183_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|176519
NZ_CP022743.1\|WP_094569256.1\|858139_859618_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022743.1\|WP_094569266.1\|870150_870993_+\|isoaspartyl-peptidase/L-asparaginase	unknown	unknown	gnl\|CDD\|271340
NZ_CP022743.1\|WP_094569257.1\|859715_860996_-\|replication-associated-recombination-protein-A	unknown	unknown	gnl\|CDD\|237355
NZ_CP022743.1\|WP_094569267.1\|871037_871550_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022743.1\|WP_094569260.1\|863742_864447_-\|pseudouridylate-synthase	unknown	unknown	gnl\|CDD\|211333
NZ_CP022743.1\|WP_094572842.1\|874008_876159_+\|carboxy-terminal-processing-peptidase	unknown	unknown	gnl\|CDD\|236873
NZ_CP022743.1\|WP_094569271.1\|877387_879013_+\|ATP-dependent-DNA-ligase	unknown	unknown	gnl\|CDD\|236428
NZ_CP022743.1\|WP_094569261.1\|864594_864858_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022743.1\|WP_094569268.1\|871626_872952_-\|amino-acid-permease	unknown	unknown	gnl\|CDD\|129983
NZ_CP022743.1\|WP_094569254.1\|856275_856827_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022743.1\|WP_094569270.1\|876245_877391_+\|ligase-associated-DNA-damage-response-exonuclease	unknown	unknown	gnl\|CDD\|274995
NZ_CP022743.1\|WP_094572840.1\|857394_858138_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP022743.1\|WP_157740586.1\|862339_863383_+\|DUF4097-family-beta-strand-repeat-protein	unknown	unknown	gnl\|CDD\|372574
NZ_CP022743.1\|WP_094569264.1\|866323_868951_-\|cyanophycin-synthetase	unknown	unknown	gnl\|CDD\|237586

Protein	Function_ID	Function_description	E-value
NZ_CP022743.1\|WP_094569258.1\|861059_861695_+\|DNA-3-methyladenine-glycosylase-2-family-protein	gnl\|CDD\|223200	COG0122, AlkA, 3-methyladenine DNA glycosylase/8-oxoguanine DNA glycosylase [DNA replication, recombination, and repair].	2.05793e-50
NZ_CP022743.1\|WP_157740584.1\|861705_862257_+\|sugar-O-acetyltransferase	gnl\|CDD\|100047	cd03357, LbH_MAT_GAT, Maltose O-acetyltransferase (MAT) and Galactoside O-acetyltransferase (GAT): MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively at the C6 position of the nonreducing end glucosyl moiety. GAT specifically acetylates galactopyranosides. Furthermore, MAT shows higher affinity toward artificial substrates containing an alkyl or hydrophobic chain as well as a glucosyl unit. Active MAT and GAT are homotrimers, with each subunit consisting of an N-terminal alpha-helical region and a C-terminal left-handed parallel alpha-helix (LbH) subdomain with 6 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X).	9.3106e-96
NZ_CP022743.1\|WP_094569255.1\|856856_857351_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	1.65013e-13
NZ_CP022743.1\|WP_094569265.1\|869143_870052_+\|cyanophycinase	gnl\|CDD\|131124	TIGR02069, cyanophycinase, cyanophycinase. This model describes both cytosolic and extracellular cyanophycinases. The former are part of a system in many Cyanobacteria and a few other species of generating and later utilizing a storage polymer for nitrogen, carbon, and energy, called cyanophycin. The latter are found in species such as Pseudomonas anguilliseptica that can use external cyanophycin. The polymer has a backbone of L-aspartic acid, with most Asp side chain carboxyl groups attached to L-arginine. [Energy metabolism, Other].	1.67835e-60
NZ_CP022743.1\|WP_094569266.1\|870150_870993_+\|isoaspartyl-peptidase/L-asparaginase	gnl\|CDD\|271340	cd14949, Asparaginase_2_like_3, Uncharacterized bacterial subfamily of the L-Asparaginase type 2-like enzymes, an Ntn-hydrolase family. The wider family of Asparaginase 2-like enzymes includes Glycosylasparaginase, Taspase 1, and L-Asparaginase type 2. Glycosylasparaginase catalyzes the hydrolysis of the glycosylamide bond of asparagine-linked glycoprotein. Taspase1 catalyzes the cleavage of the Mix Lineage Leukemia (MLL) nuclear protein and transcription factor TFIIA. L-Asparaginase type 2 hydrolyzes L-asparagine to L-aspartate and ammonia. The proenzymes of this family undergo autoproteolytic cleavage before a threonine to generate alpha and beta subunits. The threonine becomes the N-terminal residue of the beta subunit and is the catalytic residue.	0
NZ_CP022743.1\|WP_094569263.1\|865400_866183_-\|hypothetical-protein	gnl\|CDD\|176519	cd08577, PI-PLCc_GDPD_SF_unchar3, Uncharacterized hypothetical proteins similar to the catalytic domains of Phosphoinositide-specific phospholipaseand Glycerophosphodiester phosphodiesterases. This subfamily corresponds to a group of uncharacterized hypothetical proteins similar to the catalytic domains of Phosphoinositide-specific phospholipase C (PI-PLC), and glycerophosphodiester phosphodiesterases (GP-GDE), and also sphingomyelinases D (SMases D) and similar proteins. They hydrolyze the 3'-5' phosphodiester bonds in different substrates, utilizing a similar mechanism of general base and acid catalysis involving two conserved histidine residues.	3.89065e-64
NZ_CP022743.1\|WP_094572840.1\|857394_858138_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	1.09715e-52
NZ_CP022743.1\|WP_094569257.1\|859715_860996_-\|replication-associated-recombination-protein-A	gnl\|CDD\|237355	PRK13342, PRK13342, recombination factor protein RarA; Reviewed.	0
NZ_CP022743.1\|WP_094569271.1\|877387_879013_+\|ATP-dependent-DNA-ligase	gnl\|CDD\|236428	PRK09247, PRK09247, ATP-dependent DNA ligase; Validated.	0
NZ_CP022743.1\|WP_094572842.1\|874008_876159_+\|carboxy-terminal-processing-peptidase	gnl\|CDD\|236873	PRK11186, PRK11186, carboxy terminal-processing peptidase.	0
NZ_CP022743.1\|WP_094569268.1\|871626_872952_-\|amino-acid-permease	gnl\|CDD\|129983	TIGR00905, Arginine/ornithine_antiporter, transporter, basic amino acid/polyamine antiporter (APA) family. This family includes several families of antiporters that, rather commonly, are encoded next to decarboxylases that convert one of the antiporter substrates into the other. This arrangement allows a cycle that can remove proteins from the cytoplasm and thereby protect against acidic conditions. [Transport and binding proteins, Amino acids, peptides and amines].	4.63784e-88
NZ_CP022743.1\|WP_157740586.1\|862339_863383_+\|DUF4097-family-beta-strand-repeat-protein	gnl\|CDD\|372574	pfam13349, DUF4097, Putative adhesin. This has a putative all-beta structure with a twenty-residue repeat with a highly conserved repeating GD, gly-asp, motif. It may form part of a bacterial adhesin.	2.05311e-05
NZ_CP022743.1\|WP_094569270.1\|876245_877391_+\|ligase-associated-DNA-damage-response-exonuclease	gnl\|CDD\|274995	TIGR04122, hypothetical_protein, putative exonuclease, DNA ligase-associated. Members of this protein family frequently are found annotated as a putative exonuclease involved in mRNA processing. This protein is found, exclusively in bacteria, associated with three other proteins: an ATP-dependent DNA ligase, a helicase, and putative phosphoesterase.	0
NZ_CP022743.1\|WP_094569260.1\|863742_864447_-\|pseudouridylate-synthase	gnl\|CDD\|211333	cd02563, PseudoU_synth_TruC, tRNA pseudouridine isomerase C. Pseudouridine synthases catalyze the isomerization of specific uridines in an tRNA molecule to pseudouridines (5-ribosyluracil, psi). No cofactors are required. TruC makes psi65 in tRNAs. This psi residue is not universally conserved.	5.59981e-97
NZ_CP022743.1\|WP_094569264.1\|866323_868951_-\|cyanophycin-synthetase	gnl\|CDD\|237586	PRK14016, PRK14016, cyanophycin synthetase; Provisional.	0

>NZ_CP022743.1|WP_094569261.1|864594_864858_+|hypothetical-protein
MTKYQQANGTSIEVYFFKYRRFITILSIVLLLYFPFDIYLSPAFIPGHTYQTIGHWLNDSIIYLVVPIGLLVYLQRLRKAHVAEADR
>NZ_CP022743.1|WP_094569260.1|863742_864447_-|pseudouridylate-synthase
MPLLKILFHDEHLVAINKPHGLLVHRSSIANDATEFALQMLRDQLNRHVFPAHRLDRKTGGVLLFALSKDAEKLMQQQFSDNRVNKKYLAIVRGHTPDTEEINYPLRKENGTLQEAFTKYKTLARAELDVPLGSHPTSRYSLVEANPESGRMHQLRKHFAHVFHPIIGDRTHGCNKQNKLFKERWELDTMLLHASQLAFTHPVTQQPVHIEAPLQDEFLRVMKIMGWGLNDLAS
>NZ_CP022743.1|WP_157740586.1|862339_863383_+|DUF4097-family-beta-strand-repeat-protein
MKTYLTLFIVACQSVVALAQDNDGKAPYSTKSLANDAISSVMVSTSAGGINVSGRPGEAPRVEVYIRGNNGRELSKEEIQKRLARDYDMNIAVNGHELSATVKTKHNFSNWTQSLSISFKIFVPQQVATNLKTSGGGIVLDNLKGNETFSTSGGGLVIDKLSGVIRGRTSGGGIEVSNSSEDIDLSTSGGGIVAKNCTGKMKLITSGGGIELANLKGNIVAHTSGGGVEGRNVEGELVTGTSGGGIDLKGMSCSLDASTSAGNLDVEMKQAGKYVKLTASSGDVNLSLPLKQGLDLSLRGESVSQRPSKISGFTGEWGKNRINGSVNGGGIPVEASAGSGNLNVRFN
>NZ_CP022743.1|WP_157740584.1|861705_862257_+|sugar-O-acetyltransferase
MTEKEKMIAGLPYNANNPELVALRRDVRVKLAAYNSAGYVTETISAMLAGILGETGKGSWIEPPFYCDYGFNIKTGKDFYMNFDCVILDVAPVTIGDNVMCGPKVQLLAATHSLDPEERNFSGTELGKPITIGNRVWIGAGVIVCPGVTIGDEAVIGAGSVVTRDVPPRVFAAGNPCKVIKAI
>NZ_CP022743.1|WP_094569258.1|861059_861695_+|DNA-3-methyladenine-glycosylase-2-family-protein
MPDKFTKENYQSICDGLAAADPDLAAIIRAHSYPPFWWRPNTFETLVHIILEQQVSLASALSALKKLKERLQELTPARLLLLTGEEMRACYVSRQKSGYIKYLAEALLSGQLRLAEMEELPDEQVRAKLVALKGIGNWTADVYLMFVLQHPDIFPIGDLAAVNALKKIKNLPATVTREQIMAITMQWQPYRTIAAMLLWHYYLSAPKNKIQ
>NZ_CP022743.1|WP_094569257.1|859715_860996_-|replication-associated-recombination-protein-A
MNNLPPLAERMRPKNLDDYVGQKHLVGHGAVLRKAIASGALPSMIFWGPPGVGKTTLAYIISQTLDRPFFALSAINSGVKDVREVIEKASLLKAEGLVLPVLFIDEIHRFSKSQQDSLLGAVERGIVTLIGATTENPSFEVISALLSRCQVYILQPLDEYDLMSLLDKAMREDVVLEKKVIIVKENEALLRLSGGDARKLLNIFELLVNAFDSKKITLTNKNILEHVQQNMALYDKTGEQHYDIISAFIKSMRGSDPNGAVYWLARMIVGGEDPLFIARRMLILASEDIGNANPNALLLAQSCFEAVNKIGMPESQLILSQTAIYLATSAKSNSATTAIGAAIAMVKQTGDLPVPLHLRNAPTKLMKNIGYGKDYKYAHSYEGNFTELDFLPDAIKGTKLYNPGNNARENESKEKLKKLWGERYKY
>NZ_CP022743.1|WP_094569256.1|858139_859618_-|hypothetical-protein
MISTFFRHELKAFWRSKNTGKSIAIRVVMGLLILYLFINVLVMGFFLDKFLEKAFPHDDLVMSFCGILLFYFLFDLFARLQFQELPTLRVQPYLQLPVKRNSLVRYLAFTSLLSVFNLWPFVLFAPFIVKIIATDSGAVVALAFFISLAGLTIFNNYLALYLKRKANLNGWIFLAAAAVIILIGLSDFLWHLISIRKFSFLFFGNVITHPALAVAPVLLGTVMYYLNFLYLKENLYLEELGSRKAAKYKSSTEYPLLSRFGSVGDLAANEFKLIFRNKRSRSAFIMGLFIMFYGLIFYTNPKMNSESLSVFVSMFMTGIFVINYGQFMYSWQASHFDGLLVSKVKFADFVRAKYLMFTIISTFFLLLTTPYAYFGWKILVIEVIMYLWNIGVNTTLVLFFANRNYKRIDLSKGAAFNWEGVSGNQWILSFPLLIAPYVFYGPFALLHHENAGLALLAVISLVFIFTRSFWIKKLETDFYTKRYTIAEGFRNK
>NZ_CP022743.1|WP_094572840.1|857394_858138_-|ABC-transporter-ATP-binding-protein
MIEIKNLKKIYNGVTVVNIPGVAIATGESVGLVGNNGAGKTTLFRMMLDLIRPETGQVLMKGEPVAGNEDWKNFTASYLDEGFLIDYLTPEEYFYFIGGLHQQSRAHVDDFMAGLTDFFNGEILKKGKYIRDLSKGNQCKVGVASCLLQSPQLLMLDEPFANIDPSTQFRLKSIVKDLNKNKGVTTLISSHDLNHITDVCDRILLMEKGVIIKDIATSSSTLNELQEYFGVGQTAATHIKVDEEENH
>NZ_CP022743.1|WP_094569255.1|856856_857351_-|GNAT-family-N-acetyltransferase
MYTIRKATLNDVETIIDIAEKTWWPSYSPILEKEQISFMLGEIYSVAKIKLQIDNSSQIYLLLLEDEKPVAFAAYSPREENPEIYKLHKLYCLPETQGKGYGKVLINAVAHKTIEAGKHILDLNVNRHNKAKSFYEKMGFEVAYEEDIAIGPYWMNDYVMRKEL
>NZ_CP022743.1|WP_094569254.1|856275_856827_-|hypothetical-protein
MQTLRSPLIVIVIFATCFCLNASAQSSVDCTKLLKKEIDPDSARNMENDVADHADCFGLDSIGIKIFADRTTLRALLVKNASASTGKLTYANLLSDINKAKKDTGYYNPLRNLVIAQTTLEATKISVASWDSSVKLLKVIGMPDSEMENFHQFLLEKKDKNWNYRQLVTAYRMKQMDAPKTKN
>NZ_CP022743.1|WP_094569263.1|865400_866183_-|hypothetical-protein
MNKLKSILSLIALSFALSSCLTSNKDYTPADAHSHNDYKNSIPFYRAYDAGFGSIEADVFAVNGQLLVAHSEKEITPSRSLKRLYLDPLIAKFKRDTTRKLRLLIEIKKDYTITLPLVIEELKPLSQYLDYPGHTGRLSIVMTGAVPPGEVMLNYPAWLNFDVGHVGGFTPQQLTKIGLISVPFSHFSTWNGERDISQPDVDRLRSIIDSAHAVGKKIRFWDTPDNPACWKELIRLHSDVIGTDKINELAIYLNNKAYLE
>NZ_CP022743.1|WP_094569264.1|866323_868951_-|cyanophycin-synthetase
MKIENIQVLRGPNIWSVSRKKLIQMRLNLEDLENRPTNTIDGFYERLENLMPSLYSHRCSPGVPGGFFQRIQAGTWMGHVIEHIALEIQTLAGMETGFGRTRETKTPGIYNVVFTYLEEKVGIFAAEASVKIAEALINGDEYDLEHDIQKMREIRENTRLGPSTGSIVEEAIARDIPWIRLNNQSLVQLGYGKNQVRFRATMTEKTSSIAVDIASNKDETKRLLMEQAIPVAKGITISTIEGVDEAIRKVGFPLVFKPLDGNHGRGISINIKTHEEAVEAYEHAARISRKVIVERFVTGYDFRVLVIDNKMVAAALRDPAHVKGDGVSTIQQLIDKENEDPRRGYGHENVLTLISIDRDTLDLLEKKGYTLDTVPKKGEKVFVKSTANLSTGGTSVDVTDHVHPQNIFICERISKIIGLDICGIDIMAENLTEPLTENGGVVLEVNAAPGFRMHIAPSEGLPRNVAGHVIDMLYPPGKSARIPIIAITGTNGKTTTTRLIAHIVKNNGFRVGFTTSDGIYVQNHMMLKGDTTGPVSSEFILKDPTVDFAVLETARGGILRSGLGFGFCDIGVVTNIQEDHLGLQDIHTLDDLTRVKNVVVDAIKKDGWAVLNADNEYCVRMGKNAHCKVAYFSLHENNPIVKSHCKKGGIACIYENGFITIQKGDWKIRVQRTTLIPVTFGGTVPFMIENVLAATLATFLYDFKTEDIKISLETFIPSAAQTPGRMNIFNFRDFRFMIDFAHNPAGFKGIKAFLDHIDSPLKIGIIAGTGDRRDEDIRELGKLSAEMFDYIIIRQEKHLRGRTAENIVGLLVEGIDSVDKEKKYEVVPNEIDAIKHSMSLARPGTFIVALSDVIDNAIETVQNYQEQERNGTFNM
>NZ_CP022743.1|WP_094569265.1|869143_870052_+|cyanophycinase
MTVPKGKLIIIGGAVDMNTNLGAQEEILKPDHLKFFEQGILKRIITESARQSASKVEVITTASQIPELVGEEYTEAFNYLLANPIGVMDIRTREDASNPEYLERIRKCDVVMFSGGDQLRLSSIFGGTEFLQIMKNRYEHEHFVIAGTSAGAAAASTNMIYRGQSSKALIKGEVQITAGLGFIDSVIIDTHFVQRGRIGRLLYAVASNPGMLGIGLGEDAGLLITEGTMMEAIGSGLTILVNGRKMAETNIYDVEMGSPVSIKNMRVSVMSIFDKYDLAQSQLLIKKATKAEEGVVVTAPGS
>NZ_CP022743.1|WP_094569266.1|870150_870993_+|isoaspartyl-peptidase/L-asparaginase
MKIIIHGGFFSESLTNQEVKKAKQDALAEIVQLGHTYLQEHTALETVVYTVQLLEDCELFNAGTGSQIQSDGKIRLSASLMDGKTLKFSGVINIEDVQNPICIAEKLLAFDDRVLSGKGAHDFAREHGFNYHNPEIPQRREEYEKKLSDSIRLGTVGCVALDSDGNLAAATSTGGKGFEMPGRVSDSATTAGNYANAFAGISCTGVGEDIVSGAVASNIVIRVTDALPLAQATKKTLSELKPYDGFAGVIGISATGEIYHADTHPYMVWASYDEGVEVFA
>NZ_CP022743.1|WP_094569267.1|871037_871550_-|hypothetical-protein
MKKLILITVLLLSASLFTRAQDTTRSKAQPDSIIKVIPFGEGTHTAHLYTIGGKLQTPEDVKMRLLSYAPSAAEYNLAKSNITWGYISFTGFVASGTGAAIAFAKTSKFAGETTALVNGQPTFIYQHHNKTAAYILTGVATAFLTTAIIKLVHSGRHGNRALKLYNQRFE
>NZ_CP022743.1|WP_094569268.1|871626_872952_-|amino-acid-permease
MAEPSKKIGIWTSTSLVVGSMIGAGVFLVPSAMASYGSVSLLGWVFSAIGAFFLARVFSRLSALVPKSTGGPYAYTHHGFGDFAGFIVAWGYYISVITANAAITISFVSAMSTFFPALATNAAAAILTGLSAIWFLAWINTRGVPASGRVQLVTTILKLLPLLVISIGGLFFIRAENFHPFNSSGGSVYDAINATATITMFSFVGIECATIPADSVENPGKIIGRATMLGLLICTIVYILGSVSIMGIIPAAQLKYSVTPYADAAAIMFGNNARYWASAGMAIAAFGALNGWTLIQGKLPYAIAKDKLFPPVFGRQNKKGAPYVGIIVSSTFVSVFMMMNYTKGLVEQFRFLLLLSTLTTLVPYLFCAAAFVIIRLKIKQSKGLPAAIIVGALAFAYSIWAVAGSGQNTVYWGFLLLMAGIPFYVWATYKKNSELKDVSEV
>NZ_CP022743.1|WP_157740588.1|873145_873763_+|hypothetical-protein
MKFTLLILCSMFSLTASAQWYNIFKNHQRFPLVEQVTDHSVARIKVNTAIKPAKIHNFTLDRSEYSYQAVENMVMRTAQHNMRFRVYNDASYNFSELAKLYIQQNRYSEAKWYLLQSNIISRRQNDDKHTIANLMELAIIKSELGDYAQAQQDLTEAHDMATMRGFNTELTAIDKKMALIKQNKNNAPKTDVRYAEAAMSSSKAE
>NZ_CP022743.1|WP_094572842.1|874008_876159_+|carboxy-terminal-processing-peptidase
MFKKLYLVLVLGATLACSAKPAKHVNVDGSNNIQPDEKQAIVCKTIATLISKYNYKKVELNDSISSIVYNRYLKMMDESHNYFLASDITDFDKYKTVLDDDVKNGNLSDVFYIFNVYQKRYIDRIKYSLTQLDNDFDFSKNDNFTYNRESLPFVSSETEMNKIWSERVKYDMLNLKLAGTDAAKNKQTLKKRYESLLAQANKLNNQDVFQLFMDAFTEAIDPHTNYFNPANAANFNIEMSRQLEGIGAGLNTENEFIIIKSLTAGGPAEKSKQVNVDDRIVGVAQGADGEFQNVVGWRVENAIALIRGKKGTTVRLELLPKGLSVGSKPKVVELVREKIILKDESAKKEIRTYNENGKTVKIGVISVPAFYLDFNDYKSGNPNYKSTTHDVKLLIDSLKLEGVDGIVMDMRQNGGGSLLEAVDLTGLFIKTGPVVQVRNPNGEVEVDKDEDPSVAYAGPLAILVDRFSASATEIFSGAIQDYGRGIILGSQTYGKGSVQNAIDLDRVIPPSILERAAALVGKDKVTKTTTTGSQSVFGQLNLTIAKFYRITGNSTQHKGVTPDIAFPSVIPLDKYGEDTEPSAMPFDVIEKSAYTKVGDFNAILPQLKKLHDQRMETSPNYKYMLEDIADIKKHQTEKSVTLNEQKLKEQRDQDEKKAFEENNLRRVAMGLPVLKKGQTRPRNEDLDFLKREAGQILTDYISLDNKFTNTTPALRN
>NZ_CP022743.1|WP_094569270.1|876245_877391_+|ligase-associated-DNA-damage-response-exonuclease
MPKKPLLEFTDKGIYCAAGKFYIDPWKPVDDAVITHAHADHAYWGNKHYLAHHHSREVLLYRLGEIQLQTVEYGEKVMKNGVEISLFPAGHVIGSAQIRVEYRGEVWVVSGDYKVEDDGISTPFEPVRCNHFISECTFGMPVYQWKPQVEIFNDMNNWWRSNAEHNLATVVVGYSLGKAQRILQNLDLSIGTVYTHGVIENTNEALRRNGIILNPTSRITPDTPKEEVRKGIIIAPPSSVGTPWMRKFSPYSFGYCSGWMAIRGAKRRRAADRGFVLSDHADWDGLVSAIDATGCDSVYLTHGYTATFTRYLNGIGFDAHEVHTLYGDDEGVGSVPEEEPEVHAVSHPALSKGEGSKKDNKGTSKVLSFGEDLGEAGGHLS
>NZ_CP022743.1|WP_094569271.1|877387_879013_+|ATP-dependent-DNA-ligase
MRAFAQLFLSLDETNKTNEKVKVLKAYFNSVPDTDKMHMLALFSGRKPKRQINSTLVRKWAIEASNIPAWLFEESYHVVGDLAETMALLMPQNRGSSNKTLTEWIAEINGLGTKSEEEKKLWLFDSWAMLDSSERFVFNKLLTGSFRVGVSQSLVVKALAEITGIEAPALTHRIMGNWMPETYSFEQLVQEQNAADDISRPYPFFLAYPIQETSERQKSTDELKASLGDEAEWQAEWKWDGIRSQLIKRGGEIFIWSRGEDLATDKFPELHPFLNALPDGTVIDGELLSFQNGLPMPFNVLQTRIGRKNLSKKILEESPVAVIAYDCLEYAGEDIRNKTQTERRQILEGLQAATPFPEIFRISALISFESWGELAVVREQSRAMIAEGLMLKRKSAAYQVGRKRGDWWKWKIDPLSVDAVMIYAQKGHGRRADLYTDYTFAVWDGDKLVPFAKAYSGLTDAEINKVDYFVKRNTLEKFGPVRTVKPELVFEIGFEGINRSARHKSGIALRFPRILRWRQDKPKEEADTIESLRALLGDGEY

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Crispr_ID: NZ_CP022743_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022743_2

4995664-4995794

Orphan

Consensus_repeat	Method
CAGCCAGCCCATCCCGCGCATCATTGCGAGGAACGAAGCAACC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP022743_2

>merge|NZ_CP022743|2|4995664-4995794|CRISPRCasFinder
CAGCCAGCCCATCCCGCGCATCATTGCGAGGAACGAAGCAACCCTCTACTAAGGACAATCACGAACCTTTATGTTGATGGGGACCTTTCAGCCAGCCCATCCCGCGCGTCATTGCGAGGAACGAAGCAACC

>NZ_CP022743|2|2|4995664-4995794|CRISPRCasFinder
CAGCCAGCCCATCCCGCGCATCATTGCGAGGAACGAAGCAACC	CTCTACTAAGGACAATCACGAACCTTTATGTTGATGGGGACCTTT
CAGCCAGCCCATCCCGCGCGTCATTGCGAGGAACGAAGCAACC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022743.1\|WP_094572540.1\|4989484_4990657_+\|restriction-endonuclease	unknown	unknown	gnl\|CDD\|370247
NZ_CP022743.1\|WP_094572549.1\|5000270_5000657_-\|30S-ribosomal-protein-S9	unknown	unknown	gnl\|CDD\|376328
NZ_CP022743.1\|WP_094572554.1\|5006625_5007090_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022743.1\|WP_094572538.1\|4988050_4988281_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197775
NZ_CP022743.1\|WP_094572552.1\|5004402_5005584_-\|PAS-domain-containing-protein	unknown	unknown	gnl\|CDD\|312075
NZ_CP022743.1\|WP_094572543.1\|4994605_4994845_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022743.1\|WP_094572536.1\|4984559_4986314_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP022743.1\|WP_094572547.1\|4998436_4999288_-\|elongation-factor-Ts	unknown	unknown	gnl\|CDD\|236491
NZ_CP022743.1\|WP_094573062.1\|4986517_4987081_-\|ribosome-recycling-factor	unknown	unknown	gnl\|CDD\|178850
NZ_CP022743.1\|WP_094572537.1\|4987565_4987988_+\|DNA-mismatch-endonuclease-Vsr	unknown	unknown	gnl\|CDD\|226250
NZ_CP022743.1\|WP_094572550.1\|5000683_5001121_-\|50S-ribosomal-protein-L13	unknown	unknown	gnl\|CDD\|181703
NZ_CP022743.1\|WP_094572541.1\|4990779_4993107_+\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|372641
NZ_CP022743.1\|WP_094572546.1\|4997178_4998294_-\|N-acetylglucosamine-6-phosphate-deacetylase	unknown	unknown	gnl\|CDD\|224733
NZ_CP022743.1\|WP_094572539.1\|4988280_4989492_+\|DNA-(cytosine-5-)-methyltransferase	unknown	unknown	gnl\|CDD\|236696
NZ_CP022743.1\|WP_094572542.1\|4993110_4994262_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225114
NZ_CP022743.1\|WP_094572551.1\|5001666_5004321_+\|carboxypeptidase-like-regulatory-domain-containing-protein	unknown	unknown	gnl\|CDD\|372685
NZ_CP022743.1\|WP_094572544.1\|4995008_4995521_-\|lipocalin-family-protein	unknown	unknown	gnl\|CDD\|381213
NZ_CP022743.1\|WP_094572548.1\|4999385_5000252_-\|30S-ribosomal-protein-S2	unknown	unknown	gnl\|CDD\|235396
NZ_CP022743.1\|WP_094572545.1\|4996267_4996972_-\|UMP-kinase	unknown	unknown	gnl\|CDD\|239787
NZ_CP022743.1\|WP_094572553.1\|5005972_5006455_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP022743.1\|WP_094572540.1\|4989484_4990657_+\|restriction-endonuclease	gnl\|CDD\|370247	pfam09019, EcoRII-C, EcoRII C terminal. The C-terminal catalytic domain of the Restriction Endonuclease EcoRII has a restriction endonuclease-like fold with a central five-stranded mixed beta-sheet surrounded on both sides by alpha-helices. It cleaves DNA specifically at single 5' CCWGG sites.	2.29496e-69
NZ_CP022743.1\|WP_094572549.1\|5000270_5000657_-\|30S-ribosomal-protein-S9	gnl\|CDD\|376328	pfam00380, Ribosomal_S9, Ribosomal protein S9/S16. This family includes small ribosomal subunit S9 from prokaryotes and S16 from eukaryotes.	1.06919e-63
NZ_CP022743.1\|WP_094572538.1\|4988050_4988281_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|197775	smart00530, HTH_XRE, Helix-turn-helix XRE-family like proteins.	1.01016e-11
NZ_CP022743.1\|WP_094572552.1\|5004402_5005584_-\|PAS-domain-containing-protein	gnl\|CDD\|312075	pfam08448, PAS_4, 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.	8.15253e-10
NZ_CP022743.1\|WP_094572536.1\|4984559_4986314_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	1.49622e-132
NZ_CP022743.1\|WP_094572547.1\|4998436_4999288_-\|elongation-factor-Ts	gnl\|CDD\|236491	PRK09377, tsf, elongation factor Ts; Provisional.	4.05262e-121
NZ_CP022743.1\|WP_094573062.1\|4986517_4987081_-\|ribosome-recycling-factor	gnl\|CDD\|178850	PRK00083, frr, ribosome recycling factor; Reviewed.	2.34007e-98
NZ_CP022743.1\|WP_094572537.1\|4987565_4987988_+\|DNA-mismatch-endonuclease-Vsr	gnl\|CDD\|226250	COG3727, Vsr, DNA G:T-mismatch repair endonuclease [DNA replication, recombination, and repair].	3.97301e-63
NZ_CP022743.1\|WP_094572550.1\|5000683_5001121_-\|50S-ribosomal-protein-L13	gnl\|CDD\|181703	PRK09216, rplM, 50S ribosomal protein L13; Reviewed.	8.19201e-89
NZ_CP022743.1\|WP_094572541.1\|4990779_4993107_+\|sensor-histidine-kinase	gnl\|CDD\|372641	pfam13589, HATPase_c_3, Histidine kinase-, DNA gyrase B-, and HSP90-like ATPase. This family represents, additionally, the structurally related ATPase domains of histidine kinase, DNA gyrase B and HSP90.	5.59318e-18
NZ_CP022743.1\|WP_094572546.1\|4997178_4998294_-\|N-acetylglucosamine-6-phosphate-deacetylase	gnl\|CDD\|224733	COG1820, NagA, N-acetylglucosamine-6-phosphate deacetylase [Carbohydrate transport and metabolism].	1.52318e-116
NZ_CP022743.1\|WP_094572539.1\|4988280_4989492_+\|DNA-(cytosine-5-)-methyltransferase	gnl\|CDD\|236696	PRK10458, PRK10458, DNA cytosine methylase; Provisional.	3.35061e-134
NZ_CP022743.1\|WP_094572542.1\|4993110_4994262_+\|hypothetical-protein	gnl\|CDD\|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	0.000980237
NZ_CP022743.1\|WP_094572551.1\|5001666_5004321_+\|carboxypeptidase-like-regulatory-domain-containing-protein	gnl\|CDD\|372685	pfam13715, CarbopepD_reg_2, CarboxypepD_reg-like domain. This domain family is found in bacteria, archaea and eukaryotes, and is approximately 90 amino acids in length. The family is found in association with pfam07715 and pfam00593.	2.77641e-13
NZ_CP022743.1\|WP_094572544.1\|4995008_4995521_-\|lipocalin-family-protein	gnl\|CDD\|381213	cd19438, lipocalin_Blc-like, bacterial lipocalin Blc, Arabidopsis thaliana temperature-induced lipocalin-1, and similar proteins. Escherichia coli bacterial lipocalin (Blc, also known as YjeL) is an outer membrane lipoprotein involved in the storage or transport of lipids necessary for membrane maintenance under stressful conditions. Blc has a binding preference for lysophospholipids. This group includes eukaryotic lipocalins such as Arabidopsis thaliana temperature-induced lipocalin-1 (TIL) which is involved in thermotolerance, oxidative, salt, drought and high light stress tolerance, and is needed for seed longevity by ensuring polyunsaturated lipids integrity. This group belongs to the lipocalin/cytosolic fatty-acid binding protein family which have a large beta-barrel ligand-binding cavity. Lipocalins are mainly low molecular weight extracellular proteins that bind principally small hydrophobic ligands, and form covalent or non-covalent complexes with soluble macromolecules, as well as membrane bound-receptors. They participate in processes such as ligand transport, modulation of cell growth and metabolism, regulation of immune response, smell reception, tissue development and animal behavior. Cytosolic fatty-acid binding proteins, also bind hydrophobic ligands in a non-covalent, reversible manner, and have been implicated in intracellular uptake, transport and storage of hydrophobic ligands, regulation of lipid metabolism and sequestration of excess toxic fatty acids, as well as in signaling, gene expression, inflammation, cell growth and proliferation, and cancer development.	1.75985e-46
NZ_CP022743.1\|WP_094572548.1\|4999385_5000252_-\|30S-ribosomal-protein-S2	gnl\|CDD\|235396	PRK05299, rpsB, 30S ribosomal protein S2; Provisional.	3.5643e-140
NZ_CP022743.1\|WP_094572545.1\|4996267_4996972_-\|UMP-kinase	gnl\|CDD\|239787	cd04254, AAK_UMPK-PyrH-Ec, UMP kinase (UMPK)-Ec, the microbial/chloroplast uridine monophosphate kinase (uridylate kinase) enzyme that catalyzes UMP phosphorylation and plays a key role in pyrimidine nucleotide biosynthesis; regulation of this process is via feed-back control and via gene repression of carbamoyl phosphate synthetase (the first enzyme of the pyrimidine biosynthesis pathway). The UMP kinase of E. coli (Ec) is known to function as a homohexamer, with GTP and UTP being allosteric effectors. Like other related enzymes (carbamate kinase, aspartokinase, and N-acetylglutamate kinase) the E. coli and most bacterial and chloroplast UMPKs (this CD) have a conserved, N-terminal, lysine residue proposed to function in the catalysis of the phosphoryl group transfer, whereas most archaeal UMPKs appear to lack this residue and the Pyrococcus furiosus structure has an additional Mg ion bound to the ATP molecule which is proposed to function as the catalysis instead. Members of this CD belong to the Amino Acid Kinase Superfamily (AAK).	1.11091e-147

>NZ_CP022743.1|WP_094572544.1|4995008_4995521_-|lipocalin-family-protein
MKAVCILLISFFTLFTTLPNKTVAYVDSKRFGGTWYSLYSIPTMFDKGSRETTTHYTLNKDGYYDVVTTCIKNEKGELRTVKSKIFRVDGTTDGQMKAQFIWPIKIDYWVVDLAPDYSWAVVGHPDHRFLFIMSRKPEMDKALHEQIVAKCKAMGYPVEKLVSQGFKGAE
>NZ_CP022743.1|WP_094572543.1|4994605_4994845_+|hypothetical-protein
MNDQLENDKLNAGLQNGPANLNATIINSAASTYAYNKINNLLLMQILAKLENRDLEEIRNNVDRYVAQFTEEFMQKNLL
>NZ_CP022743.1|WP_094572542.1|4993110_4994262_+|hypothetical-protein
MIIAFDDDAAIRKSYQETLSKMGVDIKVVECATKGEVRKALKDPNIMSQVKVLIFDLSVSKEEAESLNFDILDDIKENYKKYPIPIFIHSAFAHTVEGYDDLGTLFKIDKSHNSLENIVNKIFLFYESGFLDIFSPNGFIESEMFVQIHKAFIDQFRGDEISLIIESIKSANNENFKQRTRSVFERIAIRSLYQNLLSAKKTEASNKIEEIQINAVEHYYRRKSDFSVWTGDIFKEKGSKNSLIVITPRCDINNGNNGGKYLVCNIDPLAERNISDLSKDTKTVYNYINDNPQNTGHKYRFLIPTPSFHGGKIDLTSYSTIEENSLLGEDSNYEYCISLSDELTNDVVRKYASYMLRSGISQSDITEALYYAKVEGEKTIKVA
>NZ_CP022743.1|WP_094572541.1|4990779_4993107_+|sensor-histidine-kinase
MENLNNYKFEPGARSIIQMGEELIGHPTTAINELVKNGYDADATDCKVYVNYHKDNSKSFVAISDNGLGMNSKTLFGDWLQPSVSHKRLGNSKSKIFQRNFLGSKGIGRLAAMALGRYLTVITKTSDESDYNWLVIDRQDFKAEALLSHIEFPGGSSNSANALLADERVIKKKNGISNNDLSKYLLDNKLTNFKEGTIIIVEELDDSIKTIVEDEFLNGDTEIQNIDLIQSLKILITPLILNSVIQDELINKNILEKKYEIATPESTFELFFGCNLIRSAGDTRNFIKIEEYSILSNFDYRVLGKVSKDGSINGLYYCNRLIEDSFNDSFVLSRDDVFSTEYLRTRNIDVLQDINNTNKVGEFYFDIRVFDRDPDALDKLAKLLGAPNRRSAGYLLDDIVGLRVSKDGFGVKPYGDEGNDWMELGQMRVQNPTAVIGTNQLIGNIFLFSPENDSLSEKTNREGFFENEAFITFKKMLRSILLEVGKKRYNYRQKHGLGRKAISKHDRPDSSRFLDFIKKITQDETVISQAEVYLNEISTTLDNLENSLSFSQRLATLGSGLELVYHEMSQPIMLIGKCLFSMKFPVGRINKLEDRNEILSEMTGIKSAIATLDHLKESLQPAIGISRKSNFKPVDTFDKVCYLLTKDFITYNISVDIDDNIREFKINDHEYHLWISFLNILNNSIYWLKSVENDERKILFKKGIDNELIISNNGPKIEIGELENIFNYGVTHKKVKNATGLGLAYTRSLLSTNNWEIWCENYDYGPAFILKPLKP
>NZ_CP022743.1|WP_094572540.1|4989484_4990657_+|restriction-endonuclease
MNSIAEQAILSVQKSLKSFCKFISANDAGGTGAHQSGFYIPKNSFSLLFETAGVKGSNKDRFVTIRWQNEFETTSRFIYYGTGTRNEYRLTRFGKGFPFLGEDNVGDLLIISQINVGYYEGFVLTLDDDIENFFTVFNISSNETNKLIEKTESFNAEDSLLECFLSYNKSFITDFPSTNSLSKNARDCYNISYKITDNNIKSEPDKYLLKWLDTEYQLFKSIEFKVYSEKIKTPFKSVEELVEIANTILNRRKSRAGKSLELHLAEVFNKFELLYDPQVITEDNKKPDFIFPGGKYYHDSNYDSQKLIFLASKTTCKDRWRQIINEANRIEIKHLFTLQQGISKNQLNEMYKEGVRLVVPKPYIGSFPEEYQPKILSLENFINFTSIKQT
>NZ_CP022743.1|WP_094572539.1|4988280_4989492_+|DNA-(cytosine-5-)-methyltransferase
MAAKPSQAKSNIVNNELDSAVLTHYVVTKNDVYKEKAYDITENSYGNFQEPEVLYQAIQKELFDVNDIPFPGPKPGAEKFTFIDLFAGIGGFRLALQNLGGLCLYSSEYDKYAQKTYLANFGETPFGDITKEETKSYIPKTFDVLCGGFPCQPFSIAGVSKKNSLGRKHGFEDEKQGNLFFHVAEIIEKHRPKAFFLENVKNLVSHDKGNTFKVIRQTLLDLGYSFDHRVLNGKHFVPQHRDRTIMVGFDKKVFGEDISFDFNLVKLPEANKKIKSILKEDVDPKYTLSDHLWNYLQEYAKKHKLKGNGFGFGLVNLDGISRTMSARYYKDGAEILIPQNGSAPRRLTPDECAALQGYPVNKGKKSFRIPVSDNQAYKQFGNSVVTPLIQAVGKEIVNLLQHE
>NZ_CP022743.1|WP_094572538.1|4988050_4988281_+|helix-turn-helix-transcriptional-regulator
MDIRKKIGLRIKEYRTNLKLTQEALAFKAEIDKTYVNEVENGKRNVSVINLEKIICALDATIRDFFDSEVFEGGIN
>NZ_CP022743.1|WP_094572537.1|4987565_4987988_+|DNA-mismatch-endonuclease-Vsr
MADVHSKETRSYNMSRIRSKDTRPEMLVRKFLHKNGFRYRLHVKTLPGKPDIVLPKYKTVIFIHGCFWHGHEGCKYYVVPKTRTEWWLNKIGGNILNDNNAEVLLKAAGWNIITIWECELKKSSLEATLENLINSLHKTS
>NZ_CP022743.1|WP_094573062.1|4986517_4987081_-|ribosome-recycling-factor
MSELIKKQVTDAKAHMDKAIDHCDGELQKIRAGKASPSMLDDIMVDYYGSPTPLSQVGSVNTPDARTIVVQPWEKSMLSAIEKAIMEANLGVNPQNDGVIIRINVPPLTEERRRDLAKKAKAEAESGKIAIRNIRKDANEKIRKLKTEGVSEDEMKAGEAEIQKLTDAYIIKVDVLSDAKEKDIMTV
>NZ_CP022743.1|WP_094572536.1|4984559_4986314_-|ABC-transporter-ATP-binding-protein
MKILLSYLSKHRWVVALALLMAALNIGFSLLDPYITGRIVDGVIEKRSILAYDQYIHNIIVLVSMAIGVAMVSRIAKNFQDYFTNIITQKVGAEMYADGLTHSLELPYQVFEDQRSGETLGILQKVRLDCEKFITSFISILFVSLIGMVFVIVYSVHVSYKVTLVYFAAIPIITFVSMAMSRKIKTIQKRIVSETTALAGSTTESLRNIELVKSLGLVKQEIARLNNTTYKILGLELKKVKYVRSMSFVQGTTVNFVRSVMVVVLLLLIFHGTISPGQYFSFLFYSFFLFNPLQELGNVILSWREAEVSLGNFKGILNTPIDKKPEKPVLLEKVKTLTFDNVSFKHLTANRNALNNISFETNTGETIAFVGPSGSGKTTLVKLLVGLYQPLEGDILYNNILSKEIDLDQLREKIGFVTQDTQLFSGSIRENLLFVRPGATDEECLDVLERAACQTLMARADNGLSTVIGEGGVKVSGGEKQRLSIARALLRKPDILVFDEATSSLDSITEEEITETIRDVSVLDNHITILIAHRLSTIMHADNIYVLEKGKIIESGKHLDLIAQKGLYYAMWRQQIGEKISVEA
>NZ_CP022743.1|WP_094572545.1|4996267_4996972_-|UMP-kinase
MAYKRILLKLSGESLMGDKQYGIDNKQVLQYAQDIKAVKDKGIEIAIVVGGGNIFRGLSAEKSGMERAQADYMGMLATVINCMALQNALESIGVETRLQSAIKMEQICEPYIRRRAMHHLEVGKIVIFGAGTGNPYFTTDTAASLRAIEIKADVVLKGTRVDGIYTADPEKDPAATRYDEISFQEVYDKGLNVMDMTAITLCQENNLPIIVFDMNKPGNFMKIADGEAIGTLVK
>NZ_CP022743.1|WP_094572546.1|4997178_4998294_-|N-acetylglucosamine-6-phosphate-deacetylase
MITALHNLQLISDGRITAGKVVLISGRQIVAITDESAMPDGVEQIDLKGAYLAPGLIDLQIYGSGGKLFAGTPEVDALERMENDLLNQGTTGFFATIGTNTNDIVEQGIESAKIYRERCRGNFWGLHLEGPYLNPVKKGAHPANLIKKGTLAEVKRWVEQADGVIKMMTIAPELQDQEVIDYLQAQGIILSSGHSNATYAEGKAFLNKPIPAVTHLFNAMPQMHHREPGYIPAIFEERPYTSIVADGIHVDFAMVRLAKRELGDKLFLITDAVTAATEGTYQHQFTGDRYVMPDGTLSGSCLTMLKAVQNCVEKVGIELAEALNMASLYPAQLAGLPQKGKVAAGCDADMVVFDADFRVLGTVFRGEYLKK
>NZ_CP022743.1|WP_094572547.1|4998436_4999288_-|elongation-factor-Ts
MSTVQISAADVNKLRQQTGAGMMDCKKALTETNGDFEAAIDFLRKKGAKVAASRQDRESNEGVVIARSSADGKFGVIIELNCETDFVAKNAEFIAFANLIANTAVEAKPASIEALYDLTIDVDSTTAKIGDVIIDKTGKIGEKIGVSKYAVVEGEKVVAYIHGNFRLGVLVGLSAAVAGADEAGKDVAMQIAAMNPIAIDKDGIDSTTIERELEIAKDQIRAEGKPEEMVEKISLGKLNKFYKDSTLLNQEFVKDPSKNVAQFLSTVEKGLTVTAFKRVALGA
>NZ_CP022743.1|WP_094572548.1|4999385_5000252_-|30S-ribosomal-protein-S2
MARTTYQDLLDAGVHFGHLTRKWDPKMSQYIFMERNGIHIIDLNKTLTKVEEAAAAIKQIVKSGRKVLFVATKKQAKDIVAEYAKTVNMPFITERWLGGMLTNFATVRKSIKKMSNIDKLTKDGTYSNLSKKERLMIQRERIKLETLLGGIADLNRLPAALFLIDVKKEHIAVSEALKLNIPTFAMVDTNSDPSNIDFPIPANDDATKSISLITGIIIQAIVEGLDERKREKEDEAEKEAAVAKAKADAPEAIVDRSGAAEGKRTRKVAVEADAAVEDATPTAESTEE
>NZ_CP022743.1|WP_094572549.1|5000270_5000657_-|30S-ribosomal-protein-S9
MPTTNTSGRRKTAVARIYLTDGSGAITVNGKDYKEYFPTLPLQYIVTQSTEVSGSAGKFDVKANVAGGGVKGQAEAVRLAIAKAIVELDPEKKPSLRAKGLMTRDDRMVERKKPGRKKARKRFQFSKR
>NZ_CP022743.1|WP_094572550.1|5000683_5001121_-|50S-ribosomal-protein-L13
MNTLSYKTVSANKKTVNKQWVVVDAQGEILGRLSTKIAMIIRGKTKPDFTPNVDCGDNVIVINADKVKLTGNKFSDKRYVSYTGYPGGQRFISPKELMAKHPTRVIEKAVRGMLPKSRLGKALFGNLHVYAGAEHPHEAQNPTTI
>NZ_CP022743.1|WP_094572551.1|5001666_5004321_+|carboxypeptidase-like-regulatory-domain-containing-protein
MLLIFWICAGVLTFQAKRIIGSLTVLNGKPLKILSCLWLLLAALNVAAQQTDSVKKAGGVTQVTGQVTDAATGLPLPYISITFTGSRQGVNTDKLGNFRLSAQGNFSQVTFSHLGYLSITKTIQPAQLNELEVKLHSSQTQLKEVAITSAKRQRYRNKGNPAVSLIQQIINHKDENRMESSDYLQYDQYERIGLSFFNLSQKFINGSFFSKYKFMLDTTLKINGQAQTSLPVYFSEKLSQNYYRKEPSKTIQVLNAQKQINIIKFVDTAGLDVYLNRLYGDNLDIYSNNIFIITNQFLSPIANHAPDFYKFFITDTIKTATGKLVEVSFTPRNKGDLLFEGKLLVTMDGRYAVQACELNVNKQININFMRSLKIRLDFGQYPGGRYYLNKSDVTADFGLSKTKGLGVIGERTVFYTNYKLNAPQSAQFYEGKSLQIAPNVNQNDTAYWASHRTDTLSGQQAQVYSKISRLEQMASFKRTMWLASTFTGGYATFGGLQVGPIGRFFSFNSQEGLRLQLGGRTTPQFNPSVYLEGYGAVGTKDKLAKYNLITYFSLNKTPPYRFPNDYIRVSYLYDVDVPGHSFVINNRQAALSSFHTGKTDYWLYSRIFRVSYVKDFENHFSYNLTFRNWNQQAAGTLVYQFNDANNTVVHNLTTTEADLHLRYAPHEQILQGTQERHTIYSKYPIFDVDINHGFTGIMNGSYAYTNIGANIYKRFYFSQLGYADVTLMGGYLSGKVPFPLLNISTANQSIAYDPDAYNRMNYLEFVSDHYVGLNITQAFNGFFLNKIPLVEHLKWREYLSLKILYGGLRNENNPLYSANLYKFPAAANGATGTYALGSTPYIEAGAGIGNIFKILRVDVIKRFNYLNHPGTSPYGIKFSFSPDF
>NZ_CP022743.1|WP_094572552.1|5004402_5005584_-|PAS-domain-containing-protein
MPLNQKLTLFTLKYKVIDAEHSIIGYCDAELSYCYANDAHWYWFGKMPDQIVGKMSLQNLLGPFLYGTSREYIDRVLLGRLQEFECLVVLPSGEVKKVRTKYVPDIEDGIVIGFFIYSFDVRRSDILVNQNKLQPLSNENAYDHSSVDYILEAVLRALRASILTGFPGIVKLAKRYFISETKLKTEFKKAYHTTIFIYYRNLQMEVAHDYISRRLANKGQMAMKFNFSNPSNFSACYKRFLREKEQQAEEEVNSLNPQNAINPGQYVKFIEELPTAAAVVNADFVFLGASQLWYSVFKLGTCDIKGKSLFDISPDLKVMYKKVFTECLNKTVTHLEEECLEKVDGSYGWLRWDIKPWYQSKGKVGGLLIFATDISSFKINTGKAKYFNHLNAS
>NZ_CP022743.1|WP_094572553.1|5005972_5006455_+|hypothetical-protein
MTSAQQIESQTNTLKTTEWDLLKMNFQGELNGLYYRKKKLINFFDLLYNMDAFFPAKMQLLKAGAKLTTQIRLLERLSGLADEDIQLGQSPGMDMNLMETFISKLMKNDVNKSYLALIVYLKTIEKNDIDAVTKLGHLATILNYRNFLVFLNQASLIFRY
>NZ_CP022743.1|WP_094572554.1|5006625_5007090_+|hypothetical-protein
MYLILLAFHSLVRWFVLASLLFAVYRACRGLFGKKSYTNTDEKTRIVTATIAHIQLVLGLWLYFISPVVNYFLHNFKSAVHERQIRFFGMEHITVMLTAIVLITIGSAKAKQKATSHEKFKTMAIWFIIALLLILSSIPWSFSPLISRPLFRAF

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Crispr_ID: NZ_CP022743_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022743_3

5127114-5127205

Orphan

Consensus_repeat	Method
TTCCTGAAATCCGGACGATTACC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP022743_3

>merge|NZ_CP022743|3|5127114-5127205|CRISPRCasFinder
TTCCTGAAATCCGGACGATTACCGCCGCCACCCTGGTTAGGGCCGCCGGCACCTGGGTTGTTACCCCTGTTCCTGAAATCCGGACGATTACC

>NZ_CP022743|3|3|5127114-5127205|CRISPRCasFinder
TTCCTGAAATCCGGACGATTACC	GCCGCCACCCTGGTTAGGGCCGCCGGCACCTGGGTTGTTACCCCTG
TTCCTGAAATCCGGACGATTACC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022743.1\|WP_094572638.1\|5112039_5113554_+\|glucose-6-phosphate-dehydrogenase	unknown	unknown	gnl\|CDD\|235579
NZ_CP022743.1\|WP_094572646.1\|5124067_5124820_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022743.1\|WP_094572654.1\|5135730_5137065_-\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|378963
NZ_CP022743.1\|WP_094572644.1\|5120102_5121296_-\|DUF4249-domain-containing-protein	unknown	unknown	gnl\|CDD\|379442
NZ_CP022743.1\|WP_157741055.1\|5118939_5120094_-\|DUF4249-family-protein	unknown	unknown	gnl\|CDD\|379442
NZ_CP022743.1\|WP_094572650.1\|5130233_5130656_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022743.1\|WP_094572642.1\|5116494_5118852_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|376626
NZ_CP022743.1\|WP_094572639.1\|5113651_5114374_+\|6-phosphogluconolactonase	unknown	unknown	gnl\|CDD\|238694
NZ_CP022743.1\|WP_094572655.1\|5137154_5137676_+\|putative-metal-dependent-hydrolase	unknown	unknown	gnl\|CDD\|183954
NZ_CP022743.1\|WP_094572648.1\|5128275_5129511_-\|transcription-termination/antitermination-protein-NusA	unknown	unknown	gnl\|CDD\|236410
NZ_CP022743.1\|WP_094573072.1\|5138466_5139159_+\|flavin-reductase-family-protein	unknown	unknown	gnl\|CDD\|224766
NZ_CP022743.1\|WP_094572640.1\|5114442_5115228_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022743.1\|WP_094572657.1\|5139262_5141902_+\|ligase-associated-DNA-damage-response-DEXH-box-helicase	unknown	unknown	gnl\|CDD\|274994
NZ_CP022743.1\|WP_094572637.1\|5110570_5112001_+\|NADP-dependent-phosphogluconate-dehydrogenase	unknown	unknown	gnl\|CDD\|236453
NZ_CP022743.1\|WP_094572653.1\|5132877_5135280_-\|S9-family-peptidase	unknown	unknown	gnl\|CDD\|224423
NZ_CP022743.1\|WP_094572641.1\|5115224_5116430_-\|glycoside-hydrolase-family-88-protein	unknown	unknown	gnl\|CDD\|369381
NZ_CP022743.1\|WP_094572649.1\|5129598_5130063_-\|ribosome-assembly-cofactor-RimP	unknown	unknown	gnl\|CDD\|179358
NZ_CP022743.1\|WP_094572656.1\|5137672_5138296_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022743.1\|WP_094572645.1\|5121300_5124066_-\|TonB-dependent-receptor	unknown	unknown	gnl\|CDD\|366183
NZ_CP022743.1\|WP_094572652.1\|5131161_5132730_+\|serine-hydrolase	unknown	unknown	gnl\|CDD\|224594

Protein	Function_ID	Function_description	E-value
NZ_CP022743.1\|WP_094572638.1\|5112039_5113554_+\|glucose-6-phosphate-dehydrogenase	gnl\|CDD\|235579	PRK05722, PRK05722, glucose-6-phosphate 1-dehydrogenase; Validated.	0
NZ_CP022743.1\|WP_094572642.1\|5116494_5118852_-\|hypothetical-protein	gnl\|CDD\|376626	pfam01835, A2M_N, MG2 domain. This is the MG2 (macroglobulin) domain of alpha-2-macroglobulin.	0.000165164
NZ_CP022743.1\|WP_094573072.1\|5138466_5139159_+\|flavin-reductase-family-protein	gnl\|CDD\|224766	COG1853, COG1853, Conserved protein/domain typically associated with flavoprotein oxygenases, DIM6/NTAB family [General function prediction only].	3.18779e-21
NZ_CP022743.1\|WP_094572644.1\|5120102_5121296_-\|DUF4249-domain-containing-protein	gnl\|CDD\|379442	pfam14054, DUF4249, Domain of unknown function (DUF4249). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 279 and 365 amino acids in length. There are two completely conserved residues (C and G) that may be functionally important.	5.05198e-45
NZ_CP022743.1\|WP_157741055.1\|5118939_5120094_-\|DUF4249-family-protein	gnl\|CDD\|379442	pfam14054, DUF4249, Domain of unknown function (DUF4249). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 279 and 365 amino acids in length. There are two completely conserved residues (C and G) that may be functionally important.	7.6987e-36
NZ_CP022743.1\|WP_094572652.1\|5131161_5132730_+\|serine-hydrolase	gnl\|CDD\|224594	COG1680, AmpC, Beta-lactamase class C and other penicillin binding proteins [Defense mechanisms].	3.47465e-36
NZ_CP022743.1\|WP_094572655.1\|5137154_5137676_+\|putative-metal-dependent-hydrolase	gnl\|CDD\|183954	PRK13291, PRK13291, putative metal-dependent hydrolase.	5.03941e-93
NZ_CP022743.1\|WP_094572639.1\|5113651_5114374_+\|6-phosphogluconolactonase	gnl\|CDD\|238694	cd01400, 6PGL, 6PGL: 6-Phosphogluconolactonase (6PGL) subfamily; 6PGL catalyzes the second step of the oxidative phase of the pentose phosphate pathway, the hydrolyzation of 6-phosphoglucono-1,5-lactone (delta form) to 6-phosphogluconate. 6PGL is thought to guard against the accumulation of the delta form of the lactone, which may be toxic through its reaction with endogenous cellular nucleophiles.	3.60539e-80
NZ_CP022743.1\|WP_094572648.1\|5128275_5129511_-\|transcription-termination/antitermination-protein-NusA	gnl\|CDD\|236410	PRK09202, nusA, transcription elongation factor NusA; Validated.	9.70394e-168
NZ_CP022743.1\|WP_094572654.1\|5135730_5137065_-\|FAD-dependent-oxidoreductase	gnl\|CDD\|378963	pfam12831, FAD_oxidored, FAD dependent oxidoreductase. This family of proteins contains FAD dependent oxidoreductases and related proteins.	1.00152e-24
NZ_CP022743.1\|WP_094572657.1\|5139262_5141902_+\|ligase-associated-DNA-damage-response-DEXH-box-helicase	gnl\|CDD\|274994	TIGR04121, ATP-dependent_helicase, DEXH box helicase, DNA ligase-associated. Members of this protein family are DEAD/DEAH box helicases found associated with a bacterial ATP-dependent DNA ligase, part of a four-gene system that occurs in about 12 % of prokaryotic reference genomes. The actual motif in this family is DE[VILW]H.	0
NZ_CP022743.1\|WP_094572637.1\|5110570_5112001_+\|NADP-dependent-phosphogluconate-dehydrogenase	gnl\|CDD\|236453	PRK09287, PRK09287, NADP-dependent phosphogluconate dehydrogenase.	0
NZ_CP022743.1\|WP_094572653.1\|5132877_5135280_-\|S9-family-peptidase	gnl\|CDD\|224423	COG1506, DAP2, Dipeptidyl aminopeptidases/acylaminoacyl-peptidases [Amino acid transport and metabolism].	3.12803e-64
NZ_CP022743.1\|WP_094572641.1\|5115224_5116430_-\|glycoside-hydrolase-family-88-protein	gnl\|CDD\|369381	pfam07470, Glyco_hydro_88, Glycosyl Hydrolase Family 88. Unsaturated glucuronyl hydrolase catalyzes the hydrolytic release of unsaturated glucuronic acids from oligosaccharides (EC:3.2.1.-) produced by the reactions of polysaccharide lyases.	3.97204e-09
NZ_CP022743.1\|WP_094572649.1\|5129598_5130063_-\|ribosome-assembly-cofactor-RimP	gnl\|CDD\|179358	PRK02001, PRK02001, ribosome assembly cofactor RimP.	2.12102e-40
NZ_CP022743.1\|WP_094572645.1\|5121300_5124066_-\|TonB-dependent-receptor	gnl\|CDD\|366183	pfam00593, TonB_dep_Rec, TonB dependent receptor. This model now only covers the conserved part of the barrel structure.	2.29357e-16

>NZ_CP022743.1|WP_094572646.1|5124067_5124820_-|hypothetical-protein
MNKLTSLFLAVLAFCVFFCQNVCAQVALGDSSSQQNALNNAVNLFKTSLGNQQAIYTGPEYYFYDPHIKGNAYFKEVNGFTKGSIYYDGSLYNNISMLYDLNIDQVVILLPSHVSKFSVIKERVKSFDFLGNHFVNINADSVSNNTILKSGYYNQLYNGKCEVLGKYSKSIQTTTSSISGLENYFSLSKDYYIKKDNIYRSVGGQGALLDILKDKKKELKKYIKTNNIVYRDNPEEAMVKIAAYYDQLSN
>NZ_CP022743.1|WP_094572645.1|5121300_5124066_-|TonB-dependent-receptor
MRKIYLASICFLVFLQALSAQQRNTKVFSVNFQQATIAQVVNELESKSTYHFYYDPMQFDSLRVTLQLADKPLENILDQAFKNTNFVYAVNQQQVFLTRGRQIKNELAMGYSRVQTNTQSPQTEPVADYTAEADKKVPDATTENKLYEIGIKTNNIKPGKSILSGYIRDIKSGEAVTGASIYVANTKTGAATDQFGYFSITLPRGRQTLLVRGLGMRDSRRQIILYSDGKLNIEMQEQINSLKEVKISADKVANVRSTDLGVTRLDIKNIKQIPTAFGEADVLKVVLTLPGVTSVGEATTGFNVRGGAADQNLILLDGNTIYNPAHFFGFFAAFNPDIVKDIELYKSSIPEKFGGRLSSVLDITNREGNKKKFTGSAGIGLLTSRLNVEGPLIKDKTSFIFGGRTTYSDWLLKLLPESYKHSQASFYDFNLGISHQINEKNNLYLSGYLSQDKFKLNSDTAYSYSNRNINLKWKHNFNNKLYSLISAGIDRYQYDVSSSANPVNAYDLGFKVNQSNFKTDFTYYLSNKHTLNFGLSSILYKINPGTFEPNGPKSLILPDAVPAEKALESALYLGDKYDVSDNLTISAGVRFNIYNYLGPQTVNNYAPELPREPANILDSTKYGSGSFIKTYMAPDIRVSARYLLSDNLSIKAGYNTLHQYIHLLSNSTSISPTDIYKLSDPNIKPEHGDQVSLGLFKNASANTIEMSVEVYYKRLRNYLDYKSGAVLLLNHHIEQDVINTEGKAYGAEFLLKKTAGKLNGWVSYTYSRTFLRQDDPYAGEFINSGKYYSANYDKPHSVNFNGNYRFTHRYSVSFDVSYSTGRPITLPIAKYEYAGSERVFYSDRNVYRIPDYFRSDFSIIIEGNHKVHQLTHNSWTIGVYNITGRQNAYSTFFTEQSGVISGYKLSIFAAPIPFINYNIRF
>NZ_CP022743.1|WP_094572644.1|5120102_5121296_-|DUF4249-domain-containing-protein
MKYQNFYIVFYASVVLVLSCKKPYSPPVTDTANNYLVVEGFINSGADSTMIKLNRTVKLSGNVNVNPELNAVVTVEGDDNTTSALREMPNGVYVSAGLNLNTTHKYRLRIKAAGGREYLSDFVPVVKAPPIDSITYKVQSDGVDINLNTHDVVTNTRYYRWEYDETWIFVSAFQSEYKSNGDTVLRRDLINDEIYTCWRTEHSTVITLGSSAKLSANLISDGPITFISRHSEKIKHKYSILIRQYALTKEAYDFWQILKKNTEQLGSIFDAQPSQLKGNIHAVDNALEPVIGFVSIGSFSVKRAFVDQRNLPAWIDPDDSGCKVNAYLYEYRDPVTGTTVNQVDQYINFNKATRGPIIPVEGIQPPGAPKLQGFSGSTPECVDCTLRGTNKQPGFWQ
>NZ_CP022743.1|WP_157741055.1|5118939_5120094_-|DUF4249-family-protein
MKNWKILLAGIILSVGCKKPYNPQVINSPKSYLVVEGVINTNDVSTIKVSKTVNLTSSVTTNPVQAALTIECDNGNSYSLTEINEGVYQLSGVILDNTRKFRLRITTIDDHKQYLSDYEQAKTAPPIDSIGFIVGNNKLQLYANTHDANNATHYYRFDYVETWKFHSKYDSGYISDGSAIVPRTADQQIYFCFANNASSTILLGSSAKLTQDVIFQAPLTSVESTSEKIELRYSILVHEYALTEKAYKFWDNLKKNTEQLGSIFDAEPTQLIGNIHNTADAAEPVIGYISAGTVTSKRIFISSEQLPQTWLPAYPYDCALDSAWYDNPKSHLNQVAAYLIPRIEIPVTPYFANGSISPVGYLATGIECVDCTLRGSKQQPVFWK
>NZ_CP022743.1|WP_094572642.1|5116494_5118852_-|hypothetical-protein
MIKPIQSIKAMLLTSALLLLMLNSRAQVIQEVQNSFNAYKQTALQEKVFVHTDKSTYLPGEIIWFKIYCVDGNDHKPLNLSKVVYVEVLDNSQNPIAQAKIAVKYGVGDGSIYVPVTVNSGNYKIRAYTSWMKNFSPDYYFEKKITLLNPLKSPENLGKDNANSYEIGFFPEGGNLVSGIESKVAFKAVGKNGHGVAVTGAIVNNVNDTVARFKALKFGMGSFSFTPAANNTYKAIIKFNGASATKSLPEVNSQGYVMKLTDKGDQLEVTVKGADGNVYLFAHTRQVVKAAESMTINNGMARFMVNKSLLGDGISSITIFNSAKQAVCERLYFKRPPQKLFIDAGSDQQQYALRKKVNVNVSPKDQAGKPVYANMSMAVYRIDSLQDIDRSNIFDYLWLGSDLKGNIESADYYLKNTNAEADEALDNLMLTQGWRRFDWNRVLENKPLEFNYLPEYNGHIVTAKITNTLTNTPAAGIMTYIGVPGKRVQVYASQSDSLGHLLYSTKDFYGPGEIVAQTNTTLDTTYRIDVQSPFSEQYSKVTLPKFEFLNGSQSALQAHSVGVQVLNIYSANNLKRFFTPVVDSSAFYGKPYKTYKLDDFTRFTTMEEDLREYVSEDNIVRSKGKFHIKVLNDHGFLDGDPLVLIDGVPVFDVNKIFTVDPLKVRKLEVIRDRFYYGQSAHEGIFSFTTYKGDLGGVELDPKAVVIDYEGLQLHRQFYSPVYDSETQAASRIPDFRNLLFWAPSVNNGGKLSFYTSDQAGKYVGVVQGITANGDAGSQYFTFEVK
>NZ_CP022743.1|WP_094572641.1|5115224_5116430_-|glycoside-hydrolase-family-88-protein
MKVKSLFIIIGSCLVQYCFAQPVQYLKPQPQLLNTIKKNFADAARQYKAIGANFQPGQFPRSYDPAAGKLITSNSGWWCSGFYAGTLLNLYEQEHDPALLTEANRSMDSLAKEQYNTHTHDLGFMMYCSFGNAYRLDPKPGYRQILLNSAKSLASRFNPKTGCIKSWDSKPSDFLVIIDNMMNLELLFWATKETGDSTFYKIAVTHANTTMKNHYRADYSSYHVVNYNAQTGEVLQRKTAQGYADESAWVRGQTWGLYGFTVMYRETKDKRYLQQAQHIAGFILNNPNLPPNKIPYWDFNAPNIPNALRDASAGAIMASALLELCRYTDKREAISYFNAAQTILRTLSSPEYLAVPGANGGFILMHSVGHFPQKSEIDVPLTYADYYFVEAMKRYQQFSDK
>NZ_CP022743.1|WP_094572640.1|5114442_5115228_-|hypothetical-protein
MKHWIVVVSFFSLLGLCGSANAQKVTLDYYFNHEVHKGASGNTERFHYLWDEKGNSGFSVFGDAFKKTRATLDTLGAPPTTANLKGTAIYIIVDPDTKKESPNPNYINRDDINEIAAWVKKGGVLLMMANDSANVELPHFNNLAGKFGMHFNDDLQNHVTDDNHFEEGAVVTAGNPMFKTASKIFMKDVCSISLTGPTGAALKNSGGAVIIATTKYGKGTVVAVGDPWLYNEYTNGRLPAGFENDKAANDIVAWLIKQVKK
>NZ_CP022743.1|WP_094572639.1|5113651_5114374_+|6-phosphogluconolactonase
MLNVFNTADDVLTALAEYFVILANEAIKKNKKFSVALSGGSSPKKLYELLATSYHDQVEWEKVYFFFGDERNVPQDHPDSNYLMAKKALFAPLMIEPANIFPVDTSLEPKEAAKKYQEEIEEFFDEDEQSFDLILLGLGDNSHTASLFPHTPVLHDRVPGVSEVFLQDQQVYRITLNAPLINEAQNIAFLVYGEGKAIAVHHVIEDDEDIEEYPAQLIEPIVGDIQWFLDEAAASLLRHK
>NZ_CP022743.1|WP_094572638.1|5112039_5113554_+|glucose-6-phosphate-dehydrogenase
MSTSIKSDPTIFVIFGGTGDLNSRKIAPALYNLFLDGWLPAQFSIIGTGRTKFTDEQFRDNLHNDINQFSRSGKADEKKWEEFSKNIYYQVSDINDFETYKEFGKRVEKHNAEWKTKSNVLFYLAVSPNFFPIIAANISKAKLAEDKKRVRIIIEKPFGHDLETAKELNSLLSNIFDECQIYRIDHYLGKETVQNIMAFRFANSIMEPLWNRNYIEHVQISVTEQLGVEERGDYYDGSGAMRDMIQNHLLQLLCHVAMEPPVSFNADEVRDRKVDVLKAMRKFSPEDVRNSAVRGQYGSGWMKGKEVPGYREEPKVDPDSNTETFAAIKFFVDNWRWQGVPFYLRTGKRMHQSSSVITIQFKDVPHLIFPTEAAESWQQNRLIISIQPEMSIRLQVQAKRPGLDMVLNTVDMVFDYKGTYTSQAPEAYETLILDTMLGDQTLFMRGDQVEAAWELVMPILSTWQNKKSLNFPNYSADSWGPEAAEALIARDGFTWFTIPVNGKK
>NZ_CP022743.1|WP_094572637.1|5110570_5112001_+|NADP-dependent-phosphogluconate-dehydrogenase
MSATTDKYAFGMIGLGTMGRSLLLNMADHGFAVAGHDKDAAKVASLNDEGKEKNVKGFGDVKEFIQSLTTPRAIMMLVPAGKIVDSVIEELTPLLDKGDILIDGGNSHFTDTNRRVEELEAKGLHFFGMGVSGGEEGARRGPSMMPGGDKDAYAVMKPIFEAIAAKVDGAPCVTYIGPGASGHFVKMVHNGIEYGIMQLIAETYEIMKTGLKLDNAAIGEVFAKWNEGRLKSFLLDITKDIFKYKAPGTDHLLLDDIKDEAKAKGTGKWTSQVAMDLQAPIPTVDTAVAMRDLSKYKALRVQAGDIYSKDEIKLDVNTDEFLIALEQAFYFNMIISYAQGMHLLSLASAEYKYELDLGDIAKIWRGGCIIRSEFLNDIFNAYQKDAKLVHLLLDSSVAELIKAAVPGARTVLSATVAAGVATPAYASSLSYFDAFRSKRMPSNLTQAQRDYFGAHTYELIGKEGVFHTQWTPKSED
>NZ_CP022743.1|WP_094572648.1|5128275_5129511_-|transcription-termination/antitermination-protein-NusA
MSNINLIDSFQEFKDFKNIDRPTMMSVLEDVFRSMIRKKYGTDENCDVIVNTDNGDLEIWRTRKVMEDGFSEDDDLEIELAEAKLLDPTLEVGDEHIEQITLESFGRRAILAARQTLVSKILELEKDEIFKKYKDRVGEIVTGEVYQVWKKETLVLDDEGNELLLPKSEQIPADYFKKGDSVKAVVDKVDMMNSNPKIIISRTAPEFLQRLFEQEVPEIFDGLITIKKIVREPGERAKVAVESYDDRIDPVGACVGMKGSRIHGIVRELKNENIDVINYTNNLQLYIQRALSPAKITSIKLDDEKKTAAVYLKPDQVSLAIGRGGHNIKLAGKLTGYEIDVYREADETDEDVDIEEFTDEIDSWIIDEFKRIGLDTAKSVLALTVGELVKRTDLEEETVKEVLSILQAEFE
>NZ_CP022743.1|WP_094572649.1|5129598_5130063_-|ribosome-assembly-cofactor-RimP
MNIEKRVKQLVEEKIADKPNLFLVDVKMHSNGKLMILVDGDNGIGIDECVAISRHVGFHLEEENVIETAYNLEVSSPGVDFPLASVRQYAKNIGRTLAIKMADGGKREGKLTGITEDAIIIEEKIKEKGKKAETVESVIPIDKITEAKVLISFK
>NZ_CP022743.1|WP_094572650.1|5130233_5130656_-|hypothetical-protein
MKKNGWILLLFCFACTQKPKGPVVTVSASDNNRSVKFKGLDYAILSEINRDTTRGIWENLLPVYRMPADTDLKNYQPVQHGLYTVIDSAVVFTPDTPLIKGKTYFMRYYRFKGENIWDYIKGKKRLGGVGHTDLVIKLQR
>NZ_CP022743.1|WP_094572652.1|5131161_5132730_+|serine-hydrolase
MQTFISSFLRANKRLAVAFLLFANVTLYAQTKNSLPVSKPEAEGVSAAAIDSFLNATAQSKHDFHSFMFLRHGKVVAQGWWNPYQPKLRHSLYSCSKSFTSTAIGFAVSEGRLSVSDKVVSFFPGSLPDTIKPYLAALTVKDLLTMSVGQSSDPTFAVASAKDDWVKAFLALPITYKPGSQFLYNSLATFMLSAIVQKVTGQKVVDYLKPRLFAPLGITGMDWEINKQGINTGGWGLRVQTEALAKMGQLYLQQGKWEGKQLLPAAWVAEATTFKIDQAPGAPQSKKDSSDWMQGYCYQFWRCRNNAFRADGAFGQYIIVMPKQDAVIAITSETSDMQGELNLVWKYLLPAMQRKSLPANATADDRLAKHLAALTLPPAAGASNSTNGIFNKTYTVKPNALNIRSIAFNSANGVCHLTLKKDSVTYNLDFANGKWLPGQTELQGPGLVAAAHEDFSILQPYKVVGSYGWNDSQDLQLKLRYIESPHTETIICHFNGSGLNAEVEYSFNYGNNKIALHGELLK
>NZ_CP022743.1|WP_094572653.1|5132877_5135280_-|S9-family-peptidase
MKKIFTLLLLTYCTGAFAQKLGALSIEKIMRDPKWIGTSPSNIRWTDDSKKILFKWNPANADRDELFAITPGNIKPVKVSIDEQKALVPEYGSWNKKRTLKVFEKNGDIWLSDLKTGKIQHLTSTADQENSPVFSGDESRIIFTKGDNLYSIKINSGELIQLTNFTRAAAATPVAAAGAGRRGGARKAAAEPVAGNEQERWLKSEQLELFDIIKVKDKDRKLDSIESKAFETKKLKEIATSDRSVGGVQLSPDGRYITYRLAKYPDGVKNAIVPNYVTASGFTEDIPNRTKVGGPQTTFESFVFDTQKDTVYKIVTAAIPGIKDVPAYVKDYPAELEKLTKNNEDRQVRISGPYWSEDSKYAVVEVSAQDNKDKWIMKLDPATGALSLLDREHNDAWVGGAGQGNLGWADNSHFYFESEASGYAHIYMLDLASGIKKQLTSGKWEVQTLQLSNDKKTFYFTANAEHPGITHFYRIPVSGGEPVKITGMKGGNEVTLSPDEKWLAIRYSYSNKPWELYLQANKPGAKAVQVTNSVSEEFKSYPWREPQVITFKNRYGSDVYARLYVPEKQDPAKPAVVFVHGAGYLQNVHYWWSSYFREYMFNNMLADAGYTVLDVDYSGSAGYGRDWRTAIYRHMGGKDLTDQEDGVKMLVDKYGVNPKHVGLYGGSYGGFITLMAMFTEPDTWAAGGAIRSVTDWAHYNHGYTSDILNEPYTDEKAYRLSSPIYFADGLKGNLLMLHGMVDQNVNYQDIIRLTQRLIELHKENWELASYPVEDHGFVQPSSWTDEYKRIFKLFETTLRK
>NZ_CP022743.1|WP_094572654.1|5135730_5137065_-|FAD-dependent-oxidoreductase
MIKKLTLLLLICHSTIIYAQTIKTDVLVVGSGASGIAAAIQCGRSKVKTVLADGGFKIGGGTAEGQMLAVDAGNNIASGIWGEFRKHVREFYHETAGYDTVQNHTLRSDPATATAILKKISDTVKNLAVYHDAVFGSIKKDGDRWEVMLTQNGRKLIVKARVVIDATEAGIVAAGADAKFYDGFDSQADNGNLKLYRTSIATGEYIPDQSTGDPGAVKSNYPPYPAFCIPVHAVLVQQAENILVTEKALPGDKNIQYLPLQLQLGQGVATVAAYCAFFKTTTKHLNVRIIQGELLDFKGYLLPFTDISQQDRAWRAIQQVCSTGMLRGGVQKAKFVFMPDSAVNTAEIQPVLTEIYTRAFLWFNKEKTGEKFTVGNAISFISDYTLTEPQLLTRSMQKAWKTQYKFKADFDINRPITRYEFAVLANRFLNPFARTVDLSGRLVN
>NZ_CP022743.1|WP_094572655.1|5137154_5137676_+|putative-metal-dependent-hydrolase
MTDEQMKFPIGDFKAPVSYTAEDLRKWITTIKEFPGRLRQAIINLNEKQLDTPYRTGGWTIRQVVHHCADSHMNSLLRFKWALTEDSPVVKPYEEADWALLPDYRMPVESSLKMLEGMHQHWVALLESFTENEWERSFKRPSGETIQLKKALALYAWHSKHHLAHVTETIKKF
>NZ_CP022743.1|WP_094572656.1|5137672_5138296_-|hypothetical-protein
MKKRIIKYALLTALSGSLYSCGQHSGSENTANETAVPAGEDAVDTSKIVPADKLIVPGKSAGKIVLNGSADSLVSVFGKPDFSDAGMGSVVITWYAKHDTSGYKISIFAGHNFGAKDESVAHIRKVLVTSPDFKTAEGLNTGLDLTKYQEHYKLKQISSYTDKGKKVKVYEATGKGIAFEVDSLSNKGVAIVVHQPNDSRATYINMH
>NZ_CP022743.1|WP_094573072.1|5138466_5139159_+|flavin-reductase-family-protein
MHIASEPSILYFGTPVVLIGTKNPNGTDNLAPMSSIFWLGWRCIIGLAAASKTTENLLLNRQCVLNLASVNEVAAVNRLAKTTGSNPVPDGKLLKGYRYEADKFAIAGLTKQHAATVKAPRVKECPVQMEAVVEAIHGLAADDAGQRGKIITFELRIQRVYLHEAILMDGHPNRVDPDKWKPLIMSFQQFYSLGDKVHASTLSEIPERLYNTLDRERAIKSYELSGDDER
>NZ_CP022743.1|WP_094572657.1|5139262_5141902_+|ligase-associated-DNA-damage-response-DEXH-box-helicase
MITKGQQVIRDWYRKKNWEQFAFQREMESAYLNGFSGLLNAPTGSGKTFALFLPFLADFINKHPDTYTTQGNNGLLMLWITPLRALTNDIRKAMQEVCDELGLPWRIMTRTGDTSAAEKQALKKKLPEVLLTTPESLHLMLAQKEYPKIFKGLQVVVIDEWHELLGTKRGVQVELGLSRLKALSTVGSEQLADSKDESTGNKKQPAEDCPLPTENRQLKIWGISATIGNLEQAAEVLLGNTFPPERVKMVRANLNKKLLIKSIIPENIENYSWAGHIGLKLLPQVMELVARSKTTLIFTNTRSQSEIWYHAILDNYPEYAGIMAMHHGSLDNELRNWVEQALHAEALKVVVCTSSLDLGVDFRPVDTVIQVGSPKGVARFMQRAGRSGHAPGEVSKAYFVPTHSLELLEGAALKQAIKEGIFESRDPMLLAMDVLIQYMVTLAVSDGFRADELFKEVKGTFAFADLTWNEFNQLLDFITTGGKTLAEYDEFLKVEVENGLFKVNSRRVAMRHRLSIGTITSEMSIRVKWLSGGSLGTLEESFISKLKPGNTFWFAGRSLEFIRIKEMSAYVKKSNAKKGLIPSWNGGRMPLSSQLAAVFRDKLDEVAHGIEQDEEVVALKPLFALQAQLSHLPQSHEFLIESFKSRQGHHLLFYPFEGRLVHEGMASLLAYRFSKIKTATFSIAMNDYGFELLTDEEIPIEQALEDTSFFSIDHLLEDIQHSLNANEMARRRFRDIAHIGGLVFTGYPGQQIKNKHLQASTSLLFDVFSEYEPDNLLVRQAYNEALAFQLEEFRLRMALQRIVKQNIILKTIDRPTPFAFPIMVDSLGREKLTTETLEERIAKMARQYGADEVWEEAEKSDRPKSPRARKPGVTRKKGF

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site	Prophage annotation

Anti-CRISPR protein detection

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