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_CP051626	Brevibacterium sp. 'Marine' chromosome, complete genome	4 crisprs	WYL,csa3,cas3,DEDDh,cas4,DinG	0	0	3	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP051626_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051626_1

962777-962871

Orphan

Consensus_repeat	Method
CCGTTCTTCCCTGCGTTCTTGCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051626_1

>merge|NZ_CP051626|1|962777-962871|CRISPRCasFinder
CCGTTGTGGCGACCGTTCTTCCCTGCGTTCTTGCCTCCGGGGTGGTCGCCGTCGCGGCTGCCCCAGTGGTTGCCGTTCTTCCCTGCGTTCTTTCC

>NZ_CP051626|1|1|962777-962871|CRISPRCasFinder
CCGTTGTGGCGACCGTTCTTCCC	TGCGTTCTTGCCTCCGGGGTGGTCGCCGTCGCGGCTGCCCCAGTGGTTG
CCGTTCTTCCCTGCGTTCTTTCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051626.1\|WP_051504995.1\|970829_971459_+\|uridine-kinase	unknown	unknown	gnl\|CDD\|235492
NZ_CP051626.1\|WP_169251474.1\|958512_959283_-\|IclR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224332
NZ_CP051626.1\|WP_169251484.1\|978984_980475_+\|fumarylacetoacetate-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|237193
NZ_CP051626.1\|WP_169251469.1\|953119_954613_+\|multicopper-oxidase-domain-containing-protein	unknown	unknown	gnl\|CDD\|182808
NZ_CP051626.1\|WP_169251480.1\|973315_973819_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051626.1\|WP_169253755.1\|955353_956115_+\|nucleotidyl-transferase-AbiEii/AbiGii-toxin-family-protein	unknown	unknown	gnl\|CDD\|378065
NZ_CP051626.1\|WP_169251485.1\|980456_981194_+\|GntR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224715
NZ_CP051626.1\|WP_169251476.1\|960900_962193_+\|aromatic-acid/H+-symport-family-MFS-transporter	unknown	unknown	gnl\|CDD\|340923
NZ_CP051626.1\|WP_169251482.1\|975471_977406_-\|3-hydroxybenzoate-4-monooxygenase	unknown	unknown	gnl\|CDD\|236223
NZ_CP051626.1\|WP_169251479.1\|971587_973183_+\|DUF222-domain-containing-protein	unknown	unknown	gnl\|CDD\|367155
NZ_CP051626.1\|WP_169253756.1\|965692_969097_-\|bifunctional-proline-dehydrogenase/L-glutamate-gamma-semialdehyde-dehydrogenase	unknown	unknown	gnl\|CDD\|143443
NZ_CP051626.1\|WP_039207958.1\|957834_958098_+\|DUF2277-domain-containing-protein	unknown	unknown	gnl\|CDD\|378364
NZ_CP051626.1\|WP_169251478.1\|969254_970796_+\|GntR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224715
NZ_CP051626.1\|WP_169251475.1\|959414_960872_+\|benzaldehyde-dehydrogenase	unknown	unknown	gnl\|CDD\|143470
NZ_CP051626.1\|WP_169251473.1\|958094_958481_+\|DUF1304-domain-containing-protein	unknown	unknown	gnl\|CDD\|377753
NZ_CP051626.1\|WP_169251481.1\|973922_975452_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051626.1\|WP_169251470.1\|954748_955336_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051626.1\|WP_169251471.1\|956225_956984_-\|glucose-1-dehydrogenase	unknown	unknown	gnl\|CDD\|235506
NZ_CP051626.1\|WP_169251483.1\|977451_978900_-\|MHS-family-MFS-transporter	unknown	unknown	gnl\|CDD\|340927
NZ_CP051626.1\|WP_169251472.1\|957184_957748_+\|dihydrofolate-reductase	unknown	unknown	gnl\|CDD\|223340

Protein	Function_ID	Function_description	E-value
NZ_CP051626.1\|WP_051504995.1\|970829_971459_+\|uridine-kinase	gnl\|CDD\|235492	PRK05480, PRK05480, uridine/cytidine kinase; Provisional.	4.96514e-106
NZ_CP051626.1\|WP_169251474.1\|958512_959283_-\|IclR-family-transcriptional-regulator	gnl\|CDD\|224332	COG1414, IclR, Transcriptional regulator [Transcription].	8.84418e-48
NZ_CP051626.1\|WP_169251484.1\|978984_980475_+\|fumarylacetoacetate-hydrolase-family-protein	gnl\|CDD\|237193	PRK12764, PRK12764, fumarylacetoacetate hydrolase family protein.	0
NZ_CP051626.1\|WP_169251469.1\|953119_954613_+\|multicopper-oxidase-domain-containing-protein	gnl\|CDD\|182808	PRK10883, PRK10883, FtsI repressor; Provisional.	1.09928e-96
NZ_CP051626.1\|WP_169253755.1\|955353_956115_+\|nucleotidyl-transferase-AbiEii/AbiGii-toxin-family-protein	gnl\|CDD\|378065	pfam08843, AbiEii, Nucleotidyl transferase AbiEii toxin, Type IV TA system. This family was recently identified as belonging to the nucleotidyltransferase superfamily. AbiEii is the cognate toxin of the type IV toxin-antitoxin 'innate immunity' bacterial abortive infection (Abi) system that protects bacteria from the spread of a phage infection. The Abi system is activated upon infection with phage to abort the cell thus preventing the spread of phage through viral replication. There are some 20 or more Abis, and they are predominantly plasmid-encoded lactococcal systems. TA, toxin-antitoxin, systems on plasmids function by killing cells that lose the plasmid upon division. AbiE phage resistance systems function as novel Type IV TAs and are widespread in bacteria and archaea. The cognate antitoxin is pfam13338.	3.88065e-16
NZ_CP051626.1\|WP_169251485.1\|980456_981194_+\|GntR-family-transcriptional-regulator	gnl\|CDD\|224715	COG1802, GntR, Transcriptional regulators [Transcription].	1.71802e-38
NZ_CP051626.1\|WP_169251476.1\|960900_962193_+\|aromatic-acid/H+-symport-family-MFS-transporter	gnl\|CDD\|340923	cd17365, MFS_PcaK_like, 4-hydroxybenzoate transporter PcaK and similar transporters of the Major Facilitator Superfamily. This aromatic acid:H(+) symporter subfamily includes Acinetobacter sp. 4-hydroxybenzoate transporter PcaK, Pseudomonas putida gallate transporter (GalT), Corynebacterium glutamicum gentisate transporter (GenK), Nocardioides sp. 1-hydroxy-2-naphthoate transporter (PhdT), Escherichia coli 3-(3-hydroxy-phenyl)propionate (3HPP) transporter (MhpT), and similar proteins. These transporters are involved in the uptake across the cytoplasmic membrane of specific aromatic compounds such as 4-hydroxybenzoate, gallate, gentisate (2,5-dihydroxybenzoate), 1-hydroxy-2-naphthoate, and 3HPP, respectively. The PcaK-like aromatic acid:H(+) symporter subfamily belongs to the Metazoan Synaptic Vesicle Glycoprotein 2 (SV2) and related small molecule transporter family (SV2-like) of the Major Facilitator Superfamily (MFS) of membrane transport proteins. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.7532e-81
NZ_CP051626.1\|WP_169251482.1\|975471_977406_-\|3-hydroxybenzoate-4-monooxygenase	gnl\|CDD\|236223	PRK08294, PRK08294, phenol 2-monooxygenase; Provisional.	0
NZ_CP051626.1\|WP_169251479.1\|971587_973183_+\|DUF222-domain-containing-protein	gnl\|CDD\|367155	pfam02720, DUF222, Domain of unknown function (DUF222). This family is often found associated to the N-terminus of the HNH endonuclease domain pfam01844. The function of this domain is uncertain. This family has been called the 13E12 repeat family.	3.01556e-06
NZ_CP051626.1\|WP_169253756.1\|965692_969097_-\|bifunctional-proline-dehydrogenase/L-glutamate-gamma-semialdehyde-dehydrogenase	gnl\|CDD\|143443	cd07125, ALDH_PutA-P5CDH, Delta(1)-pyrroline-5-carboxylate dehydrogenase, PutA. The proline catabolic enzymes of the aldehyde dehydrogenase (ALDH) protein superfamily, proline dehydrogenase and Delta(1)-pyrroline-5-carboxylate dehydrogenase (P5CDH, (EC=1.5.1.12 )), catalyze the two-step oxidation of proline to glutamate; P5CDH catalyzes the oxidation of glutamate semialdehyde, utilizing NAD+ as the electron acceptor. In some bacteria, the two enzymes are fused into the bifunctional flavoenzyme, proline utilization A (PutA) These enzymes play important roles in cellular redox control, superoxide generation, and apoptosis. In certain prokaryotes such as Escherichia coli, PutA is also a transcriptional repressor of the proline utilization genes.	0
NZ_CP051626.1\|WP_039207958.1\|957834_958098_+\|DUF2277-domain-containing-protein	gnl\|CDD\|378364	pfam10041, DUF2277, Uncharacterized conserved protein (DUF2277). Members of this family of hypothetical bacterial proteins have no known function.	1.96352e-38
NZ_CP051626.1\|WP_169251478.1\|969254_970796_+\|GntR-family-transcriptional-regulator	gnl\|CDD\|224715	COG1802, GntR, Transcriptional regulators [Transcription].	1.21162e-14
NZ_CP051626.1\|WP_169251475.1\|959414_960872_+\|benzaldehyde-dehydrogenase	gnl\|CDD\|143470	cd07152, ALDH_BenzADH, NAD-dependent benzaldehyde dehydrogenase II-like. NAD-dependent, benzaldehyde dehydrogenase II (XylC, BenzADH, EC=1.2.1.28) is involved in the oxidation of benzyl alcohol to benzoate. In Acinetobacter calcoaceticus, this process is carried out by the chromosomally encoded, benzyl alcohol dehydrogenase (xylB) and benzaldehyde dehydrogenase II (xylC) enzymes; whereas in Pseudomonas putida they are encoded by TOL plasmids.	0
NZ_CP051626.1\|WP_169251473.1\|958094_958481_+\|DUF1304-domain-containing-protein	gnl\|CDD\|377753	pfam06993, DUF1304, Protein of unknown function (DUF1304). This family consists of several hypothetical bacterial proteins of around 120 residues in length. The function of this family is unknown.	7.67292e-27
NZ_CP051626.1\|WP_169251471.1\|956225_956984_-\|glucose-1-dehydrogenase	gnl\|CDD\|235506	PRK05565, fabG, 3-ketoacyl-(acyl-carrier-protein) reductase; Provisional.	3.11489e-81
NZ_CP051626.1\|WP_169251483.1\|977451_978900_-\|MHS-family-MFS-transporter	gnl\|CDD\|340927	cd17369, MFS_ShiA_like, Shikimate transporter and similar proteins of the Major Facilitator Superfamily. This subfamily is composed of Escherichia coli shikimate transporter (ShiA), inner membrane metabolite transport protein YhjE, and other putative metabolite transporters. ShiA is involved in the uptake of shikimate, an aromatic compound involved in siderophore biosynthesis. It has been suggested that YhjE may mediate the uptake of osmoprotectants. The ShiA-like subfamily belongs to the Metazoan Synaptic Vesicle Glycoprotein 2 (SV2) and related small molecule transporter family (SV2-like) of the Major Facilitator Superfamily (MFS) of membrane transport proteins. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	4.71157e-153
NZ_CP051626.1\|WP_169251472.1\|957184_957748_+\|dihydrofolate-reductase	gnl\|CDD\|223340	COG0262, FolA, Dihydrofolate reductase [Coenzyme metabolism].	1.22411e-14

>NZ_CP051626.1|WP_169251476.1|960900_962193_+|aromatic-acid/H+-symport-family-MFS-transporter
MSAPSPSASTTGFASAGRWPAVLCWLAVALEGFDLVVLGAVIPELLATEALGFTPEAATMVATLSLVGVGLGAVSVGPVVDRIGRRWAIIGCVIGFSVFTLLVAFAPNVALFTICRFIAGLFLGAVMPSALAYISEYNKSGKTGKATTLTMTGYHAGAVAISLLAVAYSHNWHLLFLAGGIAGLVMVPLLIWKLPESEVFLIAQELKRNPAAAQAVDADAADPAGSVDGTVDAQVKTGMAGLFAGKLALVTIGVWAASFMGLLLVYGLNTWLPKIMADAGYEVSDSLVMLFVMNIGAVVGLVLAGWLADKHGTKKIVLMWFVLAAIFLAALSIPMTSQVLLNLAVFITGVFVFSAQVLVYAFVSAVYPPQARGTALGMASGIGRIGAIVGPFITGALVTAGIAYPWGFYLFAVVALFGFAAMAIVPRSVR
>NZ_CP051626.1|WP_169251475.1|959414_960872_+|benzaldehyde-dehydrogenase
MTDFLGTDWHEKIFTGIWTAGSGETYDVIEPATGETLGRLGAASADDVTAAATRAAAAQKEWAKTTPAERAAVLRRAGALWAEHADELAGWIIREAGSIPPKAALEISSAEAICYESSALPSHPKGQVLTSNEPRWSFARRVPAGVVSVIAPFNFPLILAMRSVAPALALGNAVLLKPDPRTAVCAGVAIAKVFAEAGLPEGLLQVLPGGLDAGEAVVAAPEVSVISFTGSTAAGRKVGEAAGRLLKRCHLELGGNNALVVLPGAEVGPATSAGAFGSWMHQGQICMTTGRHLVHDSIYDEYVEQLAERARNLPVGDPATEEVAIGPIIDEKQRTHVRDILDKATADGARLVAGGPGEGAFVPPTVLTDLSPSNPAWAQEIFGPVAPVARFSTLEEAAAMVNDSEYGLSLGILGDVGMAMDLADLVDTGKVHINEQTVSDEANVPFGGMKDSGNGSRFGGAEANIEAFTETQWVTMRSSIAPYPF
>NZ_CP051626.1|WP_169251474.1|958512_959283_-|IclR-family-transcriptional-regulator
MANSPSGDSMIDRLVRVLASFDPDHQSLSAEEIAERAELPKSTAYRLIGEMMRHDLLQRDPTGRIRIGVGMWELSNRASDAVDLASVARPHMMGVHEFVGENTQLGILREREVLIIERMSAPNAVIHRSKTAGRLPAHASSCGLVLLAYAPKHQREAYLRGPLAAITEKTTTDPASLRTMLTSIRSHHFAELSGHIDEGTTGITVPVFDAGGAAIAGLGVVIDSEHRKGVPAIMRVLRTASARITQDLANDRRFAD
>NZ_CP051626.1|WP_169251473.1|958094_958481_+|DUF1304-domain-containing-protein
MTIAGLVLAGLAAALHVFIFYLESIAWTSPRARATFGTTEAEAETTKSLAFNQGFYNLFLALTVFIGLIVFGTGAAEVGLTLVLVGAGSMVAAALVLALSSRELLASALKQGTLPLLGILCLIVGVLI
>NZ_CP051626.1|WP_039207958.1|957834_958098_+|DUF2277-domain-containing-protein
MCRNIRTLHNFEPAATSDEVHAAALQYVRKIAGTTKPSQANAEAFDAAVEEIAHTTQHLLDALVTNAPPKNREEEAEKRRARFAARA
>NZ_CP051626.1|WP_169251472.1|957184_957748_+|dihydrofolate-reductase
MGKVAWGFTCSIDGFIAGPGHDMSWLGETAETAEDTTEDMASKVAVIISGRRGYDAAKAQADIRDEMTAEPYGGAWSGTEIILTHRPEELAADASVTAMNCTITEAVERAQKIAGDRDIQIISADIARQALEVDLIDELQVYVAPVFLGDGTRIFDVPGGRRLDWELATIDEANPRSFGRTYRPKRD
>NZ_CP051626.1|WP_169251471.1|956225_956984_-|glucose-1-dehydrogenase
MADFTNKVALVTGGGSGLGEAISKDLASKGAKVVLTDINLDAAQRVADEIAEAGGTASAIQQDTSSKEDSEKVVQFAVDTYGGLNFAVNNAGIGGKQVPVGETDLDSWDKVIDVNLNGVLYGMRFQIPAMLESGAKDSAIVNMASVHGTVAAINNGAYTAAKHGVVGITKNAAAEYGAEGLRINAVGPGYITTPLLESSLDAETLEGLKAKHPLGRLGTADEVAKVVSFLLSDDASFVSGAYYLIDGGYTAV
>NZ_CP051626.1|WP_169253755.1|955353_956115_+|nucleotidyl-transferase-AbiEii/AbiGii-toxin-family-protein
MPGPDPGLLDADEASSIAEDFGVAESQVRRDHLISHVLAALSAAVSEDVIFFGGTALTRTHLTDLRLSEDIDLIAVGDRQLVAGFIQAAVSRSLRRSLGRPAFTPDLVDTRRSEPAVMSVADSRIQIQLLSQKGYPPWPTEWREIEQRYSDAPPARLTVLTAPAFAAAKLVAWNDRHASRDLYDMWAMAVNGIISSEAAELFSRHGPFTSPGAVSFASIPSEQAWTTDLAHQCRPQVTAKAAAEAVAAAWSSV
>NZ_CP051626.1|WP_169251470.1|954748_955336_+|hypothetical-protein
MRYQDARSLGTNSWRVLDDLVDQGALKRIARGVYTAPPNGQDARTWSPSLEAAALAVAASRHGSRQAILMGIGAARFWGAIPRAIGSTVVAIPVAGRRPLRVGSGTVYFAHRDLGGIDASVERTELGSGLIASREQTLFDLLMRPAQGGNPEASAEAARNLRPQIDLDEFAEVVGGSVRANDAVRRIVRGTGQKA
>NZ_CP051626.1|WP_169251469.1|953119_954613_+|multicopper-oxidase-domain-containing-protein
MKRRRHASVAAGAAVAVVVAVGLAACGVSTTSVTQAEFDNELAIPPLAESTVDDGVRTFDLTAEKGATEFPGQDGPTETWGFNGSFLGPTLRAERGEKIAVDVANDLDEPTSVHWHGMHLPAKMDGGPHQMIDPGQTWKPYWTIDQPAATLWYHPHPHGKTEDHVYKGLAGMVILDDDASTEADLPDEYGVDDLPLIVQDRSFEDGELELSHDGAEPGMLGDTVMVNGTIGGVQEVASEKVRLRLLNGSTARTYAFEFPDRTMDLIAGDGGLLGEPTEVDRLRLAPGERAEVVVDFSAGETVRMRSAEVDLGGVAVPATMGGHDSFDVLEFRAAETLKPAPEPAWSPSKHAEEDALDGPEAARTRKFELEEREINGERMDMNRIDEVAYVGDTEVWEVRSRQPIPHSFHVHDVQFDVLSVDGEAPPVEMSGRKDTIYLEPNRDYRLLMRFEDFTDPTMPYMYHCHMLLHEDEGMMGQLVVIERGQEAEVGVPAGHEH
>NZ_CP051626.1|WP_169253756.1|965692_969097_-|bifunctional-proline-dehydrogenase/L-glutamate-gamma-semialdehyde-dehydrogenase
MHTETDLATLTAQSIDTVRRWLRVSTSMTTAKNPAAERLSAVLSDDNGLDFTVGFVDRVVRTDDVHAAADALAEVGKLAPETMSYLDRAQIKAGAALAKIAPQVVVPAARTRLRQMVGHMVVDARDKQFGKTVAALTADGHRLNINLLGEAVLGDGEADNHLEQTHRLLARDDVDYVSVKVSSVASQISMWAFDETVDYVVDRLRPLYQQAAKAPTGAKFVNLDMEEYQDLELTIAVFTRLLSEPEFKDLEAGIVIQAYQPDALGAVQRLSEFASRRVENGGVGIKVRLVKGANLAMETVHAEIAGWPATTCDSKQSTDANYKRVLHWLFTPERMKGLRIGVAGHNLFDIAFAHHLSVERAVTDRVEFEMLQGMASEQAAAVTEDVGDLLLYVPAVHPKEFDVAISYLVRRLEENSASENFMSGIFDLANGNDVFKREADRFTASVNQLESILDAEGETAPAPNRHQNRSTETLGETVVPTRFFNEPDTDPSLPANQEWVRTIIAEATAPGYLDDRPNAPKVESTDALDEMIARGRAAAADWRALGAAGRAEILHRAADIFAARRGEFIAVEAAEVGKMPSQSDPEVSEAIDFIRYYALNSLELDNLEGAEFTPDEMVVITPPWNFPVAIPTGGTVAALAAGSAVIHKPSKPTPHCSALIVDCLWQAGVPKDVLQLCAPVERELGQHLVSHPDVDRVILTGASETAAMFKSFRPELHVNAETSGKNALVITPAADRDLAMADLVYSAFGHAGQKCSAASLGIMVGSTYDSERYRRQLVDAASSMVVDWPSNLASTMGPLTEDPSDKLRRALTTLEPGESWLLEPKQLDDSGRLWSPGIKDGVKPGSFFHLTEVFGPVLGLMHAKDLDEAIEFQNAVDFGLTGGIHSLDPEEVATWLDRVEVGNAYVNRGITGAIVRRQSFGGWKQSSVGLGSKAGGPNYLMLFGHFADAGNQDLEAAKADDKRWFEAEFGAAKDHTGLRAEANIFRYRPRPVTLRVTAEASLFDLERSLHAAATVDSPVQLSVAEDVAAEVKIAVTNAGVPARTESAAEFAEMVGQGRYDDTVGARIRVLGRFEDELLAAAAPRPEVAIIDEPVTTSGRVELRYYVQEQAVSMTLHRFGNPSRDFHELAATLTS
>NZ_CP051626.1|WP_169251478.1|969254_970796_+|GntR-family-transcriptional-regulator
MYSAEFRRDAVSLLTTSTLAEASARTGASPSTLRRWANRSDLEDRPRSGRPPIQETADRVVEALVATAGARISGRDYSTRALSEATGLSQSIVSRSVRALTIPVTEVSGGSELVLAASGFPLVIVGVRRIDAGGAGSREESATIVPPRRVQRRIAGITAALRIAGVGRWAQRFDSEHRQVPTAELLGLLDGDGDFLVFDPLGEVPDDLSDGAGARVAVCADFDDFVSALKSRLGECQDIPGSLLDLVADRVRHGLEGVLWRESVPYEPQRTSITSDSMEISSWLPKETRSITEHLAIALREEIIDSGYEPGDRINPRLLSRRMQVPRASVDAALRRMVDDKLLDGSRGGARIPLITTVDVLDLYAARMAIGEVVLRSLALRPQRYLVPVQLALRQVEASAPTRSGIDVEDADLHFQQELARASGLRESARAFEALTLRLRLFISILQLDYSPASDRIVSDDRAMFSALSRADAKMAIEVWRGKVDNAVRHMAGLLGRRRFDQELWTQLTRSLG
>NZ_CP051626.1|WP_051504995.1|970829_971459_+|uridine-kinase
MVYICAVETLVVGVAGGTGSGKTTLTQALLDKCEGPPSVLFHDNYYKRRDELTYAEREKVNYDDLDAFDNDLFVDHLTALRNSQAVDSPVYDFSIHNRSDETTRVEPAPVIIVEGILIFAEPRICQLLDIKLFVDTDADVRLLRRIKRDVVDRGRTLQSVEDQYLGTVKPMHELYVEPSKRNADLIIPDGGHNIVAMDMILNRIQRGVG
>NZ_CP051626.1|WP_169251479.1|971587_973183_+|DUF222-domain-containing-protein
MDVDPAREPASVPDPLTEITRIGDFLRALDPGDTEAETLERITALEELKSAVAAAQAKETVAFETLRIERDRLNRVPALDCGKRAGDEVGLAKKVSPGSGRKFLSTARSIVTGMPNTFKALAGGEISEDKVRILVDETAVLVAADRRTVDMRMKRSLGPSGLRSLRAEVRALSAEMDAEAAAKRAAKAKSNRRVNMTVIDDGIARISAILPLTRAVAAYESLRAGAETITAAGDAGGRNRQQVIADTFVERLSGQASATAVPAEIHLLVDTESLLSDGLVPAWLPGYGPLPAKTDREFIAANEAQMFISRIFTRPEDGQLVGMDAKSREFTGRLRQMITFRDDVCRTPWCDAPIRHADHAQPVAAGGETTWENGSGLCASCNYAKEHPGWTHEATADGLRVTTPSGRSYEVATPAVVRRIRFPRPVSVSEPGGSPPGSDWQQLFSRILEPDREEARRAAREDSRATVAAEEVGTDEPQASAQPEERPPRYCTRAEKIADWRRRNAHRRPSSKDCGGSMVEHQLVQVVFGPD
>NZ_CP051626.1|WP_169251480.1|973315_973819_+|hypothetical-protein
MARVLPSGAVACWVITIFVPVLDSGGPGSMRIRVTSLGFSPIDMNDLDEVYLVLWVVILTGAFTAWLLSASKWWSIAAIVLGTVLGLRLLQMVADPPIMMWDGQTADGMPTGGMEVAYPAAGFGLWVLGSLLFVAAGICGLVAAAQQDHDRRERIKRCMSKRHGPAA
>NZ_CP051626.1|WP_169251481.1|973922_975452_+|hypothetical-protein
MLWVPVAASSEDISEAPHPPRIIVTALGGPPFDLEEARVSMVLVAVGVVVCAVASSLISGRSRPDSHPWPDVVGRLWSVGTLILGACAFLVLAASLANLPTIMWDAVDDRGRPVFGTVVAQPAVGAGLWAIGGLCLLAAGVCGLLGGHRRSRVRSGTAHVPDAASPSRTEPRVTAWPRGNRTHRLAQRLPWVAVAAWVLMIWIPIFDSGDHGDERFIVTSLGSLEFLPTLLLAWAVVLICAATARAFSPFSHWSFVAGLSGVGLLIIEIVLLARPPRERVWVTDSAGEDRSALIVADPSAGVLLWTLGGCALIAAGVCGFISDRRRIERTTQRRTPGEAAERSRRLRRLARLLPLITLTAWVITLFIPVIDSFNDSGPRIIMTSLGDWSLDSTTPPDTFYLVLWALIITIAVLGLFFPSARWWAAAAMLIGALIVVLLIGLVLEPPLLMWDGQLPDGTPTGGMEIGYPSVGYGLWLVGAAALISAGICGLLAQTKRPRPAVQRPPVEGV
>NZ_CP051626.1|WP_169251482.1|975471_977406_-|3-hydroxybenzoate-4-monooxygenase
MHFHQNGYVSADPRIEEAAGYGIERSEELPDEVDVLIVGSGPAGMIAAAQLSQYPHVNTRMIEKRDSRLVIGQADGIQARSVETFQAFGFAEEIMREGYHITEMAFWNPDPENPENIIRTGRPKDDEHGISEFPHLIVNQARVLDYFAQFAAQSPGKITPDYGIEFVDLTVDQDAATASAKDHPVSVTVRYTAGERTGEERTIRAGYVVGCDGARSKVRSSIGRTMSGDQANHAWGVMDVLADSDFPDIRTKCAISSKHGNILHIPREGGHLFRMYVDLGEVPEDDARKVRSTSIDEIIRRANAIIAPYSIDVKNVAWHSVYEVGHRLTDAFDDTDETAPDSQCPRVFITGDACHTHSAKAGQGMNVSMQDGFNIAWKLGQVISGRSSTELLRTYSAERQVAAKNLIEFDKEWSTLMATPQEELPDKTYLEDFYVKTAEFPAGFMTEYTESMITTPTTHQELAVGFPIGKRFKSARVKRSCDANFIHLGHEARADGRWRVYVFADRAAPVVDSSADGSAGESKVAALAEWLASDPASPLVAFRREGEDPDALVELSVIYQQEHKEFAFPDVPQVFRPHVGAYDLEYVEKIYATLPDEDIFEAREISRDGAVVVVRPDQYVSGIFPLDAHAEIGDYFAGVFEPVK
>NZ_CP051626.1|WP_169251483.1|977451_978900_-|MHS-family-MFS-transporter
MWPGCTADARQDTGVMAAQKHTQTRVAFATIVGTSIEWYDYFLYAAASGLIFNQLFFGPLGSTLSTMVAFATVGISFLFRPLGAFLAGHFGDKLGRRVVLIITLIAMGAATALIGFLPTYESAGVLAPILLIALRIIQGISAGGEWGGAVLLAVEHADEKSRGLRGSFPQIGVSIGLLLSSGVLALMTSIAPGDAFLEWGWRVPFFLSIVLVFIGYWIRRGVEESPVFHEIAERKEQVTNPLGTLIKSHWLLVVLASLVFMGNNAAGYMTTGGYIQNYATDPAGPIGLGRGPVLWAVAASAVSWLVFTIIAGAVSDRIGRRNTYILGWILLLAGIFSLFPLVNTGSVGMLLLGLVVLTIGLGFTYGQQPAMYAELFPSSVRFSGVSVSCAIGSILGGAFAPTIAKGLVSSTGTTASVAVYLGVVAVHALAATLLLRDRTGIPLGPDHEDEQAVSPIIGIGAPQVTRDDGDRRHPADTRSYMN
>NZ_CP051626.1|WP_169251484.1|978984_980475_+|fumarylacetoacetate-hydrolase-family-protein
MSTPAGVPARPGKIIAVHVAYESRAAQRGKRPAQPSYFLKAASSVAASGQSIKRPAGTSLLAFEGEIAVVIGTSARNVTEADAWSYVAGVTASNDFGLYDMKTPDKGSNVRSKSRDGYTPLGPELIPAAEAAPDSLRLRTWVNGEVVQDDGTRADQLIFTLPRIVADLSQHLTLEPGDVILTGTPAGSSVVAPGDTVEVEVTAASANGEELSSGRLTTTVVDGPGDFDENLGSLPAVNEALTVDAWGSRVAAGLAPEGDADGTAATALDADLVAKLTEAPTAGLSAQLRSRGLNNVVIEGVAPLKPGAKIVGTAKTLRFVPNREDLFKSHGGGFNAQKQAFDSIRPGEVVVIEARGESGSGTLGDILALRAKSLGAAGVVTDGGVRDSAEVAEILPVFSTAKNPAVLGRKHVPWESDVAVACGNATVLPGDVIVADDDGAIVIPRGLVEEVVDAALAKEVEDGWVAEQVAAGNPIEELFPPKGEWKAKFDEWKASR
>NZ_CP051626.1|WP_169251485.1|980456_981194_+|GntR-family-transcriptional-regulator
MEGLTVKTEQAATAAPSLSKAETAYRWIRERVADQTYQPGHKLVLAQIALELDTSVVPVREAIRRLEADGLVTFERNVGARVAMVDQGSYTQSMEAVAILEAAAVAQAQGHLGADDLDAAEQINDRMRALLDEFEPAEFTRLNHEFHETLYRRCPNERLCTLVELEWDRLNHLRDSTFSFVPERALESVEEHSRIVALIRARASAQEVERAVREHRSATLHSFQNSQTTTAPTTDLQTDSRKDNS

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Crispr_ID: NZ_CP051626_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051626_2

2272514-2272608

Orphan

Consensus_repeat	Method
CCGTAGTTGGGCTGCGAACCGTA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051626_2

>merge|NZ_CP051626|2|2272514-2272608|CRISPRCasFinder
CCGTAGTTGGGCTGCGAACCGTACTGGGGAGCCTGCTGTCCGTATTGCTGCGAGCCGTCGTTGCCGCCCTGGCCGTAGTTCGGCTGCGAACCGTA

>NZ_CP051626|2|2|2272514-2272608|CRISPRCasFinder
CCGTAGTTGGGCTGCGAACCGTA	CTGGGGAGCCTGCTGTCCGTATTGCTGCGAGCCGTCGTTGCCGCCCTGG
CCGTAGTTCGGCTGCGAACCGTA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051626.1\|WP_169252391.1\|2274219_2275227_-\|cell-division-protein-ZapE	unknown	unknown	gnl\|CDD\|224402
NZ_CP051626.1\|WP_169252383.1\|2263912_2264509_-\|Holliday-junction-branch-migration-protein-RuvA	unknown	unknown	gnl\|CDD\|234645
NZ_CP051626.1\|WP_169252384.1\|2264573_2265170_-\|crossover-junction-endodeoxyribonuclease-RuvC	unknown	unknown	gnl\|CDD\|234587
NZ_CP051626.1\|WP_169252394.1\|2277625_2278114_-\|rRNA-maturation-RNase-YbeY	unknown	unknown	gnl\|CDD\|234575
NZ_CP051626.1\|WP_169252396.1\|2280003_2281119_-\|molecular-chaperone-DnaJ	unknown	unknown	gnl\|CDD\|237654
NZ_CP051626.1\|WP_169252386.1\|2266035_2266515_-\|NUDIX-domain-containing-protein	unknown	unknown	gnl\|CDD\|240041
NZ_CP051626.1\|WP_169252397.1\|2281246_2282287_-\|heat-inducible-transcriptional-repressor-HrcA	unknown	unknown	gnl\|CDD\|234621
NZ_CP051626.1\|WP_169253864.1\|2262839_2263883_-\|Holliday-junction-branch-migration-DNA-helicase-RuvB	unknown	unknown	gnl\|CDD\|234619
NZ_CP051626.1\|WP_169253866.1\|2278110_2279052_-\|PhoH-family-protein	unknown	unknown	gnl\|CDD\|376820
NZ_CP051626.1\|WP_169252388.1\|2268684_2269290_-\|HIT-domain-containing-protein	unknown	unknown	gnl\|CDD\|238606
NZ_CP051626.1\|WP_169252395.1\|2279245_2280007_-\|16S-rRNA-(uracil(1498)-N(3))-methyltransferase	unknown	unknown	gnl\|CDD\|367950
NZ_CP051626.1\|WP_169252389.1\|2269286_2271293_-\|threonine--tRNA-ligase	unknown	unknown	gnl\|CDD\|237050
NZ_CP051626.1\|WP_169253865.1\|2273782_2274145_+\|TIGR02611-family-protein	unknown	unknown	gnl\|CDD\|131660
NZ_CP051626.1\|WP_169252398.1\|2282447_2283311_+\|DUF3097-domain-containing-protein	unknown	unknown	gnl\|CDD\|378628
NZ_CP051626.1\|WP_169252385.1\|2265169_2265922_-\|YebC/PmpR-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl\|CDD\|234640
NZ_CP051626.1\|WP_169252392.1\|2275369_2276308_-\|GTPase-Era	unknown	unknown	gnl\|CDD\|234624
NZ_CP051626.1\|WP_169252393.1\|2276309_2277623_-\|HlyC/CorC-family-transporter	unknown	unknown	gnl\|CDD\|224173
NZ_CP051626.1\|WP_169252387.1\|2266645_2268688_-\|S9-family-peptidase	unknown	unknown	gnl\|CDD\|224423
NZ_CP051626.1\|WP_169253862.1\|2260002_2262111_-\|protein-translocase-subunit-SecD	unknown	unknown	gnl\|CDD\|235615
NZ_CP051626.1\|WP_169253863.1\|2262182_2262749_-\|preprotein-translocase-subunit-YajC	unknown	unknown	gnl\|CDD\|376903

Protein	Function_ID	Function_description	E-value
NZ_CP051626.1\|WP_169252391.1\|2274219_2275227_-\|cell-division-protein-ZapE	gnl\|CDD\|224402	COG1485, COG1485, Predicted ATPase [General function prediction only].	1.47081e-64
NZ_CP051626.1\|WP_169252383.1\|2263912_2264509_-\|Holliday-junction-branch-migration-protein-RuvA	gnl\|CDD\|234645	PRK00116, ruvA, Holliday junction branch migration protein RuvA.	1.66523e-67
NZ_CP051626.1\|WP_169252384.1\|2264573_2265170_-\|crossover-junction-endodeoxyribonuclease-RuvC	gnl\|CDD\|234587	PRK00039, ruvC, Holliday junction resolvase; Reviewed.	4.80387e-75
NZ_CP051626.1\|WP_169252394.1\|2277625_2278114_-\|rRNA-maturation-RNase-YbeY	gnl\|CDD\|234575	PRK00016, PRK00016, metal-binding heat shock protein; Provisional.	1.7875e-55
NZ_CP051626.1\|WP_169252396.1\|2280003_2281119_-\|molecular-chaperone-DnaJ	gnl\|CDD\|237654	PRK14278, PRK14278, chaperone protein DnaJ; Provisional.	1.37072e-165
NZ_CP051626.1\|WP_169252386.1\|2266035_2266515_-\|NUDIX-domain-containing-protein	gnl\|CDD\|240041	cd04685, Nudix_Hydrolase_26, Members of the Nudix hydrolase superfamily catalyze the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily requires a divalent cation, such as Mg2+ or Mn2+, for their activity and contain a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which functions as a metal binding and catalytic site. Substrates of nudix hydrolases include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance & "house-cleaning" enzymes. Substrate specificity is used to define families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required.	2.96312e-37
NZ_CP051626.1\|WP_169252397.1\|2281246_2282287_-\|heat-inducible-transcriptional-repressor-HrcA	gnl\|CDD\|234621	PRK00082, hrcA, heat-inducible transcription repressor; Provisional.	1.35495e-133
NZ_CP051626.1\|WP_169253864.1\|2262839_2263883_-\|Holliday-junction-branch-migration-DNA-helicase-RuvB	gnl\|CDD\|234619	PRK00080, ruvB, Holliday junction branch migration DNA helicase RuvB.	0
NZ_CP051626.1\|WP_169253866.1\|2278110_2279052_-\|PhoH-family-protein	gnl\|CDD\|376820	pfam02562, PhoH, PhoH-like protein. PhoH is a cytoplasmic protein and predicted ATPase that is induced by phosphate starvation.	7.17899e-135
NZ_CP051626.1\|WP_169252388.1\|2268684_2269290_-\|HIT-domain-containing-protein	gnl\|CDD\|238606	cd01275, FHIT, FHIT (fragile histidine family): FHIT proteins, related to the HIT family carry a motif HxHxH/Qxx (x, is a hydrophobic amino acid), On the basis of sequence, substrate specificity, structure, evolution and mechanism, HIT proteins are classified into three branches: the Hint branch, which consists of adenosine 5' -monophosphoramide hydrolases, the Fhit branch, that consists of diadenosine polyphosphate hydrolases, and the GalT branch consisting of specific nucloside monophosphate transferases. Fhit plays a very important role in the development of tumours. Infact, Fhit deletions are among the earliest and most frequent genetic alterations in the development of tumours.	1.74412e-65
NZ_CP051626.1\|WP_169252395.1\|2279245_2280007_-\|16S-rRNA-(uracil(1498)-N(3))-methyltransferase	gnl\|CDD\|367950	pfam04452, Methyltrans_RNA, RNA methyltransferase. RNA methyltransferases modify nucleotides during ribosomal RNA maturation in a site-specific manner. The Escherichia coli member is specific for U1498 methylation.	3.25093e-54
NZ_CP051626.1\|WP_169252389.1\|2269286_2271293_-\|threonine--tRNA-ligase	gnl\|CDD\|237050	PRK12305, thrS, threonyl-tRNA synthetase; Reviewed.	0
NZ_CP051626.1\|WP_169253865.1\|2273782_2274145_+\|TIGR02611-family-protein	gnl\|CDD\|131660	TIGR02611, Putative_membrane_protein, TIGR02611 family protein. Members of this family are Actinobacterial putative proteins of about 150 amino acids in length with three apparent transmembrane helix and an unusual motif with consensus sequence PGPGW. [Hypothetical proteins, Conserved].	1.5731e-14
NZ_CP051626.1\|WP_169252398.1\|2282447_2283311_+\|DUF3097-domain-containing-protein	gnl\|CDD\|378628	pfam11296, DUF3097, Protein of unknown function (DUF3097). This family of proteins with unknown function appears to be restricted to Actinobacteria.	1.21467e-136
NZ_CP051626.1\|WP_169252385.1\|2265169_2265922_-\|YebC/PmpR-family-DNA-binding-transcriptional-regulator	gnl\|CDD\|234640	PRK00110, PRK00110, YebC/PmpR family DNA-binding transcriptional regulator.	1.61281e-140
NZ_CP051626.1\|WP_169252392.1\|2275369_2276308_-\|GTPase-Era	gnl\|CDD\|234624	PRK00089, era, GTPase Era; Reviewed.	4.07864e-162
NZ_CP051626.1\|WP_169252393.1\|2276309_2277623_-\|HlyC/CorC-family-transporter	gnl\|CDD\|224173	COG1253, TlyC, Hemolysins and related proteins containing CBS domains [General function prediction only].	8.55023e-87
NZ_CP051626.1\|WP_169252387.1\|2266645_2268688_-\|S9-family-peptidase	gnl\|CDD\|224423	COG1506, DAP2, Dipeptidyl aminopeptidases/acylaminoacyl-peptidases [Amino acid transport and metabolism].	3.87541e-75
NZ_CP051626.1\|WP_169253862.1\|2260002_2262111_-\|protein-translocase-subunit-SecD	gnl\|CDD\|235615	PRK05812, secD, preprotein translocase subunit SecD; Reviewed.	6.03546e-115
NZ_CP051626.1\|WP_169253863.1\|2262182_2262749_-\|preprotein-translocase-subunit-YajC	gnl\|CDD\|376903	pfam02699, YajC, Preprotein translocase subunit. See.	7.23329e-18

>NZ_CP051626.1|WP_169252389.1|2269286_2271293_-|threonine--tRNA-ligase
MADSIDCAGESIPFTEGLTGTEIFSTDRTVVAMWLNGEPADLSRELQSGDRIAPITIDSDAGLDILRHSTGHVTAQAVQELFPGTKLGIGPYITDGYYFDFDAAEPFTPEDLKAIQKKAAQIVKSGQTFNRVVVTEDEARERMANEPFKLELIDDKGKGGDEETSVEVGGGELTVYENVDRKGEVVWQDLCRGPHLPNTKLIGNGFAITRSSAAYWRGDQANASLQRVYGTAWASKDDLKAYQDRIAEAERRDHRKLGAEMDLFSFPEELGSGLPVFHPKGGVIKREMEDYVRARHIAEGFEYVGTPHISKETLYYTSGHLPYYGENMFPAMSVDEIRDESGQVVKEGTPYRLKAMNCPMHNLIYRSRGRSYRDLPLRLFEFGTVYRDEASGVIHGLTRVRALTQDDSHSYVAQEDAGKEIRHLLNFVLSLLRDFGLDDFYLELSTRDEDGKKADKFIGSDEQWAEATSVLEEVAQETGLELVPDPGGAAFYGPKISVQARDAIGRTWQMSTVQLDFNQPERFGLEYVAADGSRKQPVMIHSAKFGSIERFLGVLTEHYAGAFPVWLAPVQVTCIPVADEFNDYLAEVADQLRRSGVRVELDDSDDRFPKKIRNASKSKVPFTLIAGGEDRDAGAVSFRFRSGEQENGVPVAEAVRRILDTIETKAQV
>NZ_CP051626.1|WP_169252388.1|2268684_2269290_-|HIT-domain-containing-protein
MSGGDDDRTAQENSGGRLGEGIAYPEAAAGFPGEPDGFQRLWTPHRMVYIDGQDKPKDDRADECPFCTAPSKTDADGLIVARGQHVYAVLNLYPYNPGHLLICPYRHVADYTDLSHDETVELAEFTQKAMRVIRAVSGPHGFNLGMNQGPVAGAGIAAHLHQHVVPRWGGDANFLPVIAQTKALPQVHADVQARLQKEWNR
>NZ_CP051626.1|WP_169252387.1|2266645_2268688_-|S9-family-peptidase
MNPEDLGTLAEYSSPMLRGSDTVITIRRPDLETNSYLAQLFSLDADRSRRLTHSWSDSNPQCGPNWSGYLSAEKKAAPQLFAGDSLETAHQITDNHLGVAEFALDDSRARALYVARVAEPGRYGLDDAVPAAEEAPRRITTASYLANGLGYTNDRPARAFLVDLAEPGIGTVGLRGASEVPLSTLLTTPDTDVHDPRFSPGGHWASVIAAAEPDRGRPDLRSTVWLLGREESHPLDLPPMSLSLHVWIDTERVLLLGNALSRDELDFVGQMPGLFLHDMTTGSTTRLTDPETVALAPIRPQIYGGAVVAAVDTDGATRIVRIGLDAAQVALDDLEFLTDDTTAVNGFDLDEETLVFTGSTPRSPAVLGRISLDARADSGAASVMGETVIVKEHPAPANSVEPQVLRVPGVSGTITGWLAKPHGEGPFPVILNIHGGPFAQYTHSWFDETQVLTSAGYAVVYSNPRGSGGRTRSWGTAVQGDMAAPAMADVLAVLDHALDSDPTLDRSRLGIQGGSYGGYLTAMTIAADHRFRAAIVERGYLDPDSFVGTSDIGRFFTEEYTGRSREAIAAQSPLAHAPQVGTPTLVMHSELDLRCPLEQAQQYYAALQRAGVDTEMLIFPGENHELSRAGQPRHRRQRFEAILDWWDRHFSGGIRTQPEGERHRSDAADPGAASAADSAS
>NZ_CP051626.1|WP_169252386.1|2266035_2266515_-|NUDIX-domain-containing-protein
MKPRKASRVVLLNERDEVLLIRAQDLLTPSHQWWMTCGGGSELGESAAQTAARELAEETGIECEPHELIGPLATRDEVFEFTEKSLRQVETYFAFRTTEDIELEDAVWTDIEKRSLLEFRWWTREELLATTETIYPKNLLGLIDLATAGSVPDVPLVID
>NZ_CP051626.1|WP_169252385.1|2265169_2265922_-|YebC/PmpR-family-DNA-binding-transcriptional-regulator
MSGHSKWATTKHKKAAIDAKRGKLFAKLIKNIEVAARNGGPDPDGNPTLFDAIQKAKKNSVPADNITRAVKRGGGLDGSGVNYETIMYEGYAAGGVALLIECLTDNRNRAASEVRVAVTRNGGSMADPGSVTYNFNRKGVITVGAEETDEEAILLATMDAGAEEVKEVGEKFEIICEATDLVAVRTALVDAGIDYDSAEASFVPELEVSLDAETARKVFSLIDALEDSDEVQNVYSNADVSDEVLAELDA
>NZ_CP051626.1|WP_169252384.1|2264573_2265170_-|crossover-junction-endodeoxyribonuclease-RuvC
MRILGVDPGLTRCGLGVIDTLPARKATMVAVDVLRTPSADSVDLRLGAIAEAFDTWLDTYRPDVVAIERVFARNDVSTIMGTAQASGLTMGLAARRGLPVAMHTPSEVKAAITGSGRADKKQVTSMVTRILGLEAPPKPADAADALAIAICHSWRGALAAQSTPGKNKDLTERKSGGRQGSGLTKAQQQWAEAMRRAK
>NZ_CP051626.1|WP_169252383.1|2263912_2264509_-|Holliday-junction-branch-migration-protein-RuvA
MISFLSGTVHRIAADHLVVLTYGVGRKVHVTPDTLAGTRHGAEIELVTSLVVREDSMTLFGFTTEDENHTFEVLLSISGIGPRLAMAILSVMGPDELAAAITNQDANALTRVPGIGKKGASRIILELENKLPKLTAAAPGPTLSFGGGNQQVVDALVGLGWKEPQAEEVVAEVVKETGADAGTSVILKAALKVLGAKR
>NZ_CP051626.1|WP_169253864.1|2262839_2263883_-|Holliday-junction-branch-migration-DNA-helicase-RuvB
MDFGDQDLTGAEQERLVSGRAETAERDAEAALRPKGLADFIGQPQVREQLSLVLDAAKARQKAPDHVLLSGPPGLGKTTLAMIIAHEMNSSLRVTSGPAVQHAGDLAAILSSLEEGEVLFIDEIHRMARAAEEMLYVAMEDFRVDVIVGKGPGATAIPLDLPQFTLVGATTRSGLLPAPLRDRFGFTALLDFYSSADLLTVLRRSAKMLGIESELAGLEEISTRSRGTPRIANRLLRRVRDWAQVRGSGIIDEEAATNALRVYEVDELGLDRLDRSVLHVLCQRFGGGPVGLGTLAVSVGEEADTVETVSEPYLVREGLISRTPRGRVATSAAWNHLKMQIPANYEF
>NZ_CP051626.1|WP_169253863.1|2262182_2262749_-|preprotein-translocase-subunit-YajC
MIPLALAALLIFFLFNSRRKQKARAEQIKSGLVPGATVMTTFGVFGTVLSIDEENNQVTIESGPGTVLRVHRQAIGQIENNQAAAPVDAPGADAPAADVDAAADDEKPAITDAELDAMNERKRAEKDTADDETAEDISADESAAKTEDADAVAEAEDVDIDAAETDADSAAADDDSTDSTDSDSDKKN
>NZ_CP051626.1|WP_169253862.1|2260002_2262111_-|protein-translocase-subunit-SecD
MRFLWLTIITVVLAAIIAGGVIWSNATTTPKLALDLEGGTSIILEPQVSEGTDISKEQLDQAVAIIRQRVDSTGVSEAEITTQGDRNIVVNLPGNPDEETRNLVRSSAQLVFRRVALVGDPRSQEQIQKEQEKSGEESGADDGLSDEERKRLEDLTGADSQGDGQGEDQAPSGGGDVVEAGGSATKTDESTEETKSSESASKDAEKSGEGSGSSEGSKVTDSTPRPLFDPEKDASEWQTDAIIKEYTELDCTNKKNRTGGQQQPSDEPVVSCSEDGQAKYILGPVELSGDHLADANAGYAAGANGVQTNNPAVNLSFDSTGREIFKQITSDITGKQQPYNQFAIELDGLVLSAPSSNAVITDGNAQITGNFTLDEAQTLANQLKNGSLPLSFQVQSEDQISPTLGSNYLKIGLLTGLVGLLLVVVYSLLQYRVLGLVTVSSLVVAGVLTYLLLLLASWRYGYRLSLAGVAGIIIGIGMAADSFIVYFERVRDELRSGRNLLSAVEVGWDRAKRTIYASKAVNMLAAVILYILAVGSVRGFAFTLGLTVIIDVLIVFLFTHPMLQFLARTKFFGEGHPMSGMDPRLLGVKPAAYRGALNLSIDDQDKSPEAKRREKARLRKAGMTAEDGSDTTAAAAASESEETTTDESKASTAAKSKSAESKPAKTATGGMTIAERKAAARRAEEEHAAEDSAAADGKEDDK
>NZ_CP051626.1|WP_169253865.1|2273782_2274145_+|TIGR02611-family-protein
MLANPHTARLYRSIVGGLGTLIVLIGLVLVPLPGPGWLIVIIGLFIISSEFHWARRLLHFVRVNVERWTHWIMAQRLWVRWTVGAVTAAFVTAIVWLTLRLTGLPDWVPDLRIFDVIGLS
>NZ_CP051626.1|WP_169252391.1|2274219_2275227_-|cell-division-protein-ZapE
MNAEQTLVALSDRSPQVAPEELIAGLVPPPQFEDVSFDSYRTDPAEPSQEEARNRLREFTERSTGQGFFGKLFSKGKSGAKGVYLDGGYGVGKTHLLASAWHANEKPATFGTFVEYTNLVGALGFARARDDLSAMKLVCVDEFELDDPGDTVLMSRLMRELTDAGVKIIATSNTLPGSLGEGRFAAQDFLREIQALADQFEVYRIDGKDYRARELTAPADPLPESELDAAASRLDGVVARDDFSQLLSHLSTVHPSRYGRMVDGIDAAVWENVRTIDNESVALRFVALVDRLYDRNVPIINSGAALDKVFTDESLAGGYKKKYMRCLSRLTALSS
>NZ_CP051626.1|WP_169252392.1|2275369_2276308_-|GTPase-Era
MEFRTDYPEDYRAGFACFVGRPNTGKSTLTNALVGEKVAITSAKPQTTRHTIRGVVHKDDHQLILIDTPGLHKPRTLLGSRLNDLVASTLGEVDVIGFCLPADEPIGPGDRYIASQLALLDGRTPIVALVTKVDRVPKDKIAEALLAVGELADFADVVPVSAVEDFQVDTVDSVLAAHLPKSPPLYPDGDLTDEPEEKMIAELVREAALEGVRDELPHSLAVQVEEMYPREGRSEDNPLWNVHVNLYVERPSQKAIIIGKGGSRLKAIGSESRQGIERLLGTKVYLDLHVKVAKDWQRDPKQLGRLGFDFNS
>NZ_CP051626.1|WP_169252393.1|2276309_2277623_-|HlyC/CorC-family-transporter
MFMFFLGAALCLIIAATLSAVDAALLNVSHHAVEEAKEDGKRSAVRVERILADLPTNINVIIFVRNFLEALATVFIALAYDSYYSVGPLMVFLTVITASVAVFIIAGVSPRTIGKRRSLAVSLNLSWVVRIVLVALKPLARILVVLGNLLTPDKVYKDGPFVTSEQLRDLVERASESDIIEDGEREMIQSVFNLSDTSANEVMVPRTDLITVDADVSLQKTMNLFFRSGFSRIPVCGEDLDDVRGVAYLKDVARRLHLHPEEAERPVGNLARTVLFVPETKPADDLLRQMQLDSTHLAILIDEYGGTAGLVTIEDIVEEIVGEIEDEYDNGDDELVAGDDGSFIISTRMSISDFADYFDVRIDEDDVNSVGGLLSKLIDRVPIDGSHASIAGLEIEAMEGQGRRHRITHVRVTRTHEDSRDDAQTAAAGGSGTKEED
>NZ_CP051626.1|WP_169252394.1|2277625_2278114_-|rRNA-maturation-RNase-YbeY
MNTEILNETDAEVDLDEVVALTEYLGGALHMHPGAELAVTMVDSSAMSELHVTWMDLEGPTDVMSFPMDQLHRGEPGTPTEGQMGDVIICPEVAEAQARAAGHSTMDEILLLTVHGFLHLLGYDHGEPEEREEMFALQRHLLLTFFAARYDGRTDIPTPTEV
>NZ_CP051626.1|WP_169253866.1|2278110_2279052_-|PhoH-family-protein
MRLVIPDSIDLVAFFGPGESNLRALEKTFDDLDIHVRANQVQVTGDPQRVEAFVSVIGELKKLHAAGHRINEETIERVTTFSSEGAAASAVLGTNILSTRGKSIRPKTMGQHDYVRAIRNHTITFGIGPAGTGKTYLAMAMAVNALQHKEVSRIILTRPAVEAGESLGYLPGTLNDKIDPYVRPLYDALHDMVDPESIPLLIETGTIEVAPLAYMRGRTLNDAFIILDEAQNTTAEQMKMFLTRLGFGSRMVVTGDISQIDLPGKTRSGLKVVRDILDGIDDLQFCELGSKDVVRHSLVTKIVEAYDLWGSAE
>NZ_CP051626.1|WP_169252395.1|2279245_2280007_-|16S-rRNA-(uracil(1498)-N(3))-methyltransferase
MSLPVFRSATAAEAVVGSALTFGEDVAGHAVRVRRIGPGEGIDIVDGDGTRVRGTVTAASANELTIDVTAVTNEDSTGPRLVLVQALAKGDRDLQAIETATEIGVDDVIPWAAERSIADWPAKKREKMAAKWENLLNAASLQARRSRFPVLRELVRGASLATVFDESDAVFVLHETAQRRLSAALADLIADGSSPLPKRIVFVVGPEGGISDGELEALTGRGARPVLLGPTILRSSSAGPAGLVLAQNSLGRW
>NZ_CP051626.1|WP_169252396.1|2280003_2281119_-|molecular-chaperone-DnaJ
MADHYETLGVSKDASAAEIKSSYRKLARKYHPDVNPGHEDEFKAISLAYDVLSDPEKRRNYDMGGGENGQGFPAGGGFGGFGDIFETFFGGGGGQAGGPIPRTQRGKDALVGVNIDLKTAAFGGTVDLDVTTAVVCDTCSGAGTQEGTKIETCSLCHGAGSVQRMTRTLLGQMVTNQTCNSCHGFGTVIPNPCLNCQGDGRVRKQRTMKIRIPAGVSDGTRIQLGSQGEVGPGGGPAGDLFVEVMVTRHDVFQRDGDNLRAAVSVPMTAATLGATIPFETFDGTQDLTIAAGTQSGTVVKLPGLGASRLRSETRGDLLITVDVLTPDSLDDEQRELLEKLAELRGEEAPRAQISTENRGMFSRMRERFAGR
>NZ_CP051626.1|WP_169252397.1|2281246_2282287_-|heat-inducible-transcriptional-repressor-HrcA
MNDSRRAQVLRAIVEDFVATNEPVGSKAIVQRHTLGVSPATIRNDMAQLEQEGYIAQPHTSAGRIPTDLGYRMFVDRIDEFKPLTTAERRAIFQLIDGDVDLDEMLDRTVRVLSGLTRQVALIQYPTVSRARIKHVEIVGLGPGRILVVLITDAGQVEQKSVITPTPLDEDAVRGLRDQINAEFAGRTLAQVFGSAPTAEAVAAESSEAAGRDESGLTQIRAAVVDLVAATREERIIMAGTANLARSGSEFGEKMAPILEAFEEQVVLLRLLTSMAEDHEGISVRIGRENTHESFSSTSVVAAEYGHDAGSSARLAVLGPTRMDYPTTISAVRAVAKYVSSILDRG
>NZ_CP051626.1|WP_169252398.1|2282447_2283311_+|DUF3097-domain-containing-protein
MPVNAFDRYGPDVLSGSSPSSHRPKKSRQVELGLGMVLEDAMSGYVGAVVGAEKTTAGVVVKLEDRVGKVRAFPLGPGFLLEGQPVDVQLPKKEAQQPGRTASGSRAVVGAKARVARGSRIWVEGKHDAELVEKIWGDDLRIEGVVVEPLGGLDDVADKLAAFGPDREHRVGVLADHLVTGTKESKIAEAVRADPRYRDVVHIIGHPYVDIWQAVKPHVVGIRQWPVVPRGEDWKTGILRRIGWPHADHRDVARGWVRILGKVSTIADVEPTLSGRVEELIDFVTVG

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Crispr_ID: NZ_CP051626_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051626_3

2587272-2587361

Orphan

Consensus_repeat	Method
CGTCCGCTGGGTAGGTGGGCCGC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051626_3

>merge|NZ_CP051626|3|2587272-2587361|CRISPRCasFinder
CGTCCGCTGGGTAGGTGGGCCGCTTCGGTGGGCGTTCCCTTCGCCGAGGTGGCCCCGCGGTTCCGCACGTCCGCTGGGTGGGTGGGCCGC

>NZ_CP051626|3|3|2587272-2587361|CRISPRCasFinder
CGTCCGCTGGGTAGGTGGGCCGC	TTCGGTGGGCGTTCCCTTCGCCGAGGTGGCCCCGCGGTTCCGCA
CGTCCGCTGGGTGGGTGGGCCGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051626.1\|WP_169252593.1\|2586133_2587177_-\|phenylalanine--tRNA-ligase-subunit-alpha	unknown	unknown	gnl\|CDD\|234780
NZ_CP051626.1\|WP_169252589.1\|2581096_2581789_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051626.1\|WP_169252587.1\|2574964_2575906_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|153232
NZ_CP051626.1\|WP_062861908.1\|2576013_2576325_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224278
NZ_CP051626.1\|WP_169252596.1\|2590242_2590716_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051626.1\|WP_169253889.1\|2578251_2580675_-\|aminodeoxychorismate-synthase-component-I	unknown	unknown	gnl\|CDD\|215481
NZ_CP051626.1\|WP_169252598.1\|2591859_2592978_+\|nucleotide-binding-protein	unknown	unknown	gnl\|CDD\|378409
NZ_CP051626.1\|WP_169252588.1\|2577400_2578255_-\|aminotransferase-class-IV	unknown	unknown	gnl\|CDD\|376449
NZ_CP051626.1\|WP_169252597.1\|2590737_2591397_-\|pentapeptide-repeat-containing-protein	unknown	unknown	gnl\|CDD\|224276
NZ_CP051626.1\|WP_169252602.1\|2597701_2599147_+\|sodium/solute-symporter	unknown	unknown	gnl\|CDD\|271369
NZ_CP051626.1\|WP_169252590.1\|2581805_2582336_-\|GIY-YIG-nuclease-family-protein	unknown	unknown	gnl\|CDD\|198380
NZ_CP051626.1\|WP_169252586.1\|2573885_2574599_+\|amino-acid-racemase	unknown	unknown	gnl\|CDD\|224707
NZ_CP051626.1\|WP_169253890.1\|2595323_2596550_+\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|366534
NZ_CP051626.1\|WP_169252591.1\|2582478_2583360_-\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|212491
NZ_CP051626.1\|WP_169252592.1\|2583546_2586132_-\|phenylalanine--tRNA-ligase-subunit-beta	unknown	unknown	gnl\|CDD\|234804
NZ_CP051626.1\|WP_169252595.1\|2589093_2590188_+\|MerR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|133382
NZ_CP051626.1\|WP_169252594.1\|2587425_2589060_+\|acetolactate-synthase-large-subunit	unknown	unknown	gnl\|CDD\|236239
NZ_CP051626.1\|WP_169252601.1\|2597053_2597458_+\|zinc-binding-dehydrogenase	unknown	unknown	gnl\|CDD\|176227
NZ_CP051626.1\|WP_169252599.1\|2594075_2595101_-\|AsnC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|214628
NZ_CP051626.1\|WP_169252600.1\|2596763_2597099_+\|alcohol-dehydrogenase-catalytic-domain-containing-protein	unknown	unknown	gnl\|CDD\|176227

Protein	Function_ID	Function_description	E-value
NZ_CP051626.1\|WP_169252593.1\|2586133_2587177_-\|phenylalanine--tRNA-ligase-subunit-alpha	gnl\|CDD\|234780	PRK00488, pheS, phenylalanyl-tRNA synthetase subunit alpha; Validated.	0
NZ_CP051626.1\|WP_169252601.1\|2597053_2597458_+\|zinc-binding-dehydrogenase	gnl\|CDD\|176227	cd08266, Zn_ADH_like1, Alcohol dehydrogenases of the MDR family. This group contains proteins related to the zinc-dependent alcohol dehydrogenases. However, while the group has structural zinc site characteristic of these enzymes, it lacks the consensus site for a catalytic zinc. NAD(P)(H)-dependent oxidoreductases are the major enzymes in the interconversion of alcohols and aldehydes, or ketones. Alcohol dehydrogenase in the liver converts ethanol and NAD+ to acetaldehyde and NADH, while in yeast and some other microorganisms ADH catalyzes the conversion acetaldehyde to ethanol in alcoholic fermentation. ADH is a member of the medium chain alcohol dehydrogenase family (MDR), which has a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The NAD(H)-binding region is comprised of 2 structurally similar halves, each of which contacts a mononucleotide. A GxGxxG motif after the first mononucleotide contact half allows the close contact of the coenzyme with the ADH backbone. The N-terminal catalytic domain has a distant homology to GroES. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit, a catalytic zinc at the active site, and a structural zinc in a lobe of the catalytic domain. NAD(H)-binding occurs in the cleft between the catalytic and coenzyme-binding domains at the active site, and coenzyme binding induces a conformational closing of this cleft. Coenzyme binding typically precedes and contributes to substrate binding. In human ADH catalysis, the zinc ion helps coordinate the alcohol, followed by deprotonation of a histidine, the ribose of NAD, a serine, then the alcohol, which allows the transfer of a hydride to NAD+, creating NADH and a zinc-bound aldehyde or ketone. In yeast and some bacteria, the active site zinc binds an aldehyde, polarizing it, and leading to the reverse reaction.	9.08893e-41
NZ_CP051626.1\|WP_169252587.1\|2574964_2575906_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|153232	cd03138, GATase1_AraC_2, AraC transcriptional regulators having a Type 1 glutamine amidotransferase (GATase1)-like domain. A subgroup of AraC transcriptional regulators having a Type 1 glutamine amidotransferase (GATase1)-like domain. AraC regulators are defined by a AraC-type helix-turn-helix DNA binding domain at their C-terminal. AraC family transcriptional regulators are widespread among bacteria and are involved in regulating diverse and important biological functions, including carbon metabolism, stress responses and virulence in different microorganisms. The catalytic triad typical of GATase1 domains is not conserved in this GATase1-like domain. However, in common with typical GATase1domains a reactive cys residue is found in the sharp turn between a beta strand and an alpha helix termed the nucleophile elbow.	2.07886e-57
NZ_CP051626.1\|WP_062861908.1\|2576013_2576325_+\|hypothetical-protein	gnl\|CDD\|224278	COG1359, COG1359, Uncharacterized conserved protein [Function unknown].	0.0030776
NZ_CP051626.1\|WP_169253889.1\|2578251_2580675_-\|aminodeoxychorismate-synthase-component-I	gnl\|CDD\|215481	PLN02889, PLN02889, oxo-acid-lyase/anthranilate synthase.	0
NZ_CP051626.1\|WP_169252594.1\|2587425_2589060_+\|acetolactate-synthase-large-subunit	gnl\|CDD\|236239	PRK08322, PRK08322, acetolactate synthase large subunit.	0
NZ_CP051626.1\|WP_169252588.1\|2577400_2578255_-\|aminotransferase-class-IV	gnl\|CDD\|376449	pfam01063, Aminotran_4, Amino-transferase class IV. The D-amino acid transferases (D-AAT) are required by bacteria to catalyze the synthesis of D-glutamic acid and D-alanine, which are essential constituents of bacterial cell wall and are the building block for other D-amino acids. Despite the difference in the structure of the substrates, D-AATs and L-ATTs have strong similarity.	2.01918e-33
NZ_CP051626.1\|WP_169252597.1\|2590737_2591397_-\|pentapeptide-repeat-containing-protein	gnl\|CDD\|224276	COG1357, COG1357, Pentapeptide repeats containing protein [Function unknown].	3.95412e-08
NZ_CP051626.1\|WP_169252602.1\|2597701_2599147_+\|sodium/solute-symporter	gnl\|CDD\|271369	cd11475, SLC5sbd_PutP, Na(+)/proline cotransporter PutP and related proteins; solute binding domain. Escherichia coli PutP catalyzes the Na+-coupled uptake of proline with a stoichiometry of 1:1. The putP gene is part of the put operon; this operon in addition encodes a proline dehydrogenase, allowing the use of proline as a source of nitrogen and/or carbon. This subfamily also includes the Bacillus subtilis Na+/proline cotransporter (OpuE) which has an osmoprotective instead of catabolic role. Expression of the opuE gene is under osmotic control and different sigma factors contribute to its regulation; it is also a putative CcpA-activated gene. This subfamily belongs to the solute carrier 5 (SLC5) transporter family.	1.50081e-92
NZ_CP051626.1\|WP_169252590.1\|2581805_2582336_-\|GIY-YIG-nuclease-family-protein	gnl\|CDD\|198380	cd00719, GIY-YIG_SF, GIY-YIG nuclease domain superfamily. The GIY-YIG nuclease domain superfamily includes a large and diverse group of proteins involved in many cellular processes, such as class I homing GIY-YIG family endonucleases, prokaryotic nucleotide excision repair proteins UvrC and Cho, type II restriction enzymes, the endonuclease/reverse transcriptase of eukaryotic retrotransposable elements, and a family of eukaryotic enzymes that repair stalled replication forks. All of these members contain a conserved GIY-YIG nuclease domain that may serve as a scaffold for the coordination of a divalent metal ion required for catalysis of the phosphodiester bond cleavage. By combining with different specificity, targeting, or other domains, the GIY-YIG nucleases may perform different functions.	1.92683e-05
NZ_CP051626.1\|WP_169252586.1\|2573885_2574599_+\|amino-acid-racemase	gnl\|CDD\|224707	COG1794, RacX, Aspartate racemase [Cell envelope biogenesis, outer membrane].	2.64147e-80
NZ_CP051626.1\|WP_169253890.1\|2595323_2596550_+\|diguanylate-cyclase	gnl\|CDD\|366534	pfam01244, Peptidase_M19, Membrane dipeptidase (Peptidase family M19).	4.82743e-65
NZ_CP051626.1\|WP_169252591.1\|2582478_2583360_-\|SDR-family-oxidoreductase	gnl\|CDD\|212491	cd05233, SDR_c, classical (c) SDRs. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human prostaglandin dehydrogenase (PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, PGDH numbering) and/or an Asn (Asn-107, PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	3.33488e-34
NZ_CP051626.1\|WP_169252592.1\|2583546_2586132_-\|phenylalanine--tRNA-ligase-subunit-beta	gnl\|CDD\|234804	PRK00629, pheT, phenylalanyl-tRNA synthetase subunit beta; Reviewed.	0
NZ_CP051626.1\|WP_169252595.1\|2589093_2590188_+\|MerR-family-transcriptional-regulator	gnl\|CDD\|133382	cd01107, HTH_BmrR, Helix-Turn-Helix DNA binding domain of the BmrR transcription regulator. Helix-turn-helix (HTH) multidrug-efflux transporter transcription regulator, BmrR and YdfL of Bacillus subtilis, and related proteins; N-terminal domain. Bmr is a membrane protein which causes the efflux of a variety of toxic substances and antibiotics. BmrR is comprised of two distinct domains that harbor a regulatory (effector-binding) site and an active (DNA-binding) site. The conserved N-terminal domain contains a winged HTH motif that mediates DNA binding, while the C-terminal domain binds coactivating, toxic compounds. BmrR shares the N-terminal DNA binding domain with other transcription regulators of the MerR superfamily that promote transcription by reconfiguring the spacer between the -35 and -10 promoter elements.	1.62092e-30
NZ_CP051626.1\|WP_169252598.1\|2591859_2592978_+\|nucleotide-binding-protein	gnl\|CDD\|378409	pfam10137, TIR-like, Predicted nucleotide-binding protein containing TIR-like domain. Members of this family of bacterial nucleotide-binding proteins contain a TIR-like domain. Their exact function has not, as yet, been defined.	4.76288e-24
NZ_CP051626.1\|WP_169252599.1\|2594075_2595101_-\|AsnC-family-transcriptional-regulator	gnl\|CDD\|214628	smart00344, HTH_ASNC, helix_turn_helix ASNC type. AsnC: an autogenously regulated activator of asparagine synthetase A transcription in Escherichia coli).	1.34796e-16
NZ_CP051626.1\|WP_169252600.1\|2596763_2597099_+\|alcohol-dehydrogenase-catalytic-domain-containing-protein	gnl\|CDD\|176227	cd08266, Zn_ADH_like1, Alcohol dehydrogenases of the MDR family. This group contains proteins related to the zinc-dependent alcohol dehydrogenases. However, while the group has structural zinc site characteristic of these enzymes, it lacks the consensus site for a catalytic zinc. NAD(P)(H)-dependent oxidoreductases are the major enzymes in the interconversion of alcohols and aldehydes, or ketones. Alcohol dehydrogenase in the liver converts ethanol and NAD+ to acetaldehyde and NADH, while in yeast and some other microorganisms ADH catalyzes the conversion acetaldehyde to ethanol in alcoholic fermentation. ADH is a member of the medium chain alcohol dehydrogenase family (MDR), which has a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The NAD(H)-binding region is comprised of 2 structurally similar halves, each of which contacts a mononucleotide. A GxGxxG motif after the first mononucleotide contact half allows the close contact of the coenzyme with the ADH backbone. The N-terminal catalytic domain has a distant homology to GroES. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit, a catalytic zinc at the active site, and a structural zinc in a lobe of the catalytic domain. NAD(H)-binding occurs in the cleft between the catalytic and coenzyme-binding domains at the active site, and coenzyme binding induces a conformational closing of this cleft. Coenzyme binding typically precedes and contributes to substrate binding. In human ADH catalysis, the zinc ion helps coordinate the alcohol, followed by deprotonation of a histidine, the ribose of NAD, a serine, then the alcohol, which allows the transfer of a hydride to NAD+, creating NADH and a zinc-bound aldehyde or ketone. In yeast and some bacteria, the active site zinc binds an aldehyde, polarizing it, and leading to the reverse reaction.	5.89459e-15

>NZ_CP051626.1|WP_169252593.1|2586133_2587177_-|phenylalanine--tRNA-ligase-subunit-alpha
MTDQLDPLDESAVKQAVDAALKAFTDATTLDELKQAKIDHTGDKAPLALANRAIGSLDKADKAAAGKIVGKSRGAVKQAHDVRLAELEAERDAAVLIEEAIDVTLPTDRRRLGARHPLSLIQEQAADYFVGLGWEVAEGPEIESEWLNFDALNFGPDHPARQMQDTFFVDPADAGLVLRTHTSPVQSRSLLQRGVPLYVVCPGKTFRTDELDATHTPVFHQIEGIAIDKGLTMANLQGTLDGFAREMFGPESKTRLRPSFFPFTEPSAEMDFWFPNKVGGPGWIEWGGCGMVHPNVLRAAGIDPDVYQGFAFGMGIERTLMLREGINDMHDMVEGDVRFSARFGMKA
>NZ_CP051626.1|WP_169252592.1|2583546_2586132_-|phenylalanine--tRNA-ligase-subunit-beta
MRVPLNWLADYVDLPAETDPHALAAEFASIGLEEEDFFGPEITGPLVVGRVLELVKEEHSNGKTVNWCRVDVGPEHNEAQDDPKDPQPGPEVPSRGIICGAHNFVPGDLIVACLPGAVLPGDFKIAARKTYGHKSDGMICSAKELGLGEDHDGIIVLTDLGLTGEPGDDAIALLGLDQVTLDVNVTPDRGYQLSIRGIGREYAQMKGQKFTDIGSAEVAPTNAATDDGFPVSVEDNNPINEVAGCDQFTALQITGLDPQAKTPFWMQRRLQQAGMRPISLTVDVTNYVMLELGQPLHAYDTALLGDEIVVRRATAGEKFTTLDDVERKLDPEDLLITDRGSGATGKAGKIIGLAGVMGGAEVEVNDQTTDVVIEAAHFDPISIARTSRRHKLSSEASRRFERGVDPRLGPVAARRCADLLVELGGGTLSPATTQVGQAPEPTVIELPVERVDSLVGVDYTTAEVTGLLEGIGATIDVIGKDRLAVTVPSWRTDITDAVDLIEEVARTGGYDRIPSIQPAARAGKGLTVAQKTRRRISNLLAADGFTEVLSYPFTNEKRDDQLRLDADDVRRKHVRLANPMSEDLPLMRTNLLSTLVDLVVRNQGRGAKDVALFEAGLVSTSAGLPEGPGPRHLPGYHPSDDELEAIYASVPHQPYHYAGIISGNAEMPGVWGKGRKAEATDVIDTVRRIAETNGLEVTVEADQIAPWHPGRAAKFVLADGQVLGHAGELHPKVCENLGLPARTVAFEIDLDALLAQDDLRAWDGALSTYPVSRQDVALIVDAELPTQTLAATLREGAGEELELLETFDLYTGDQLPEGKKSLAFRLTFRAPDRTLKADEASAMREAATKLAAERHGAEVRS
>NZ_CP051626.1|WP_169252591.1|2582478_2583360_-|SDR-family-oxidoreductase
MSEKLPYGTNMPTTDGTSEATAVPSETIALITGGARGIGRHLSEAFAKAGYDVIVTATSAEKAEAAADEIAEATGGAVTGVGLRTDDITAVNQLRDSVAELEKSTGKRLQVLINNAGRIESTEGPLWDADPESLKDVVDANVLGVALMINVFAPVLMAGAQATGRLSRIIDLNSGSGAKGTPAYAVYSASKAALFRIADSVVHFGHDKGLRIFEMAPGVVETAMTKSMPVHDFRQGDDWTSTEQVTGLALALASGTLDAFTGRYVRAGADTEESLLVEAADGLSDTTRRLVLG
>NZ_CP051626.1|WP_169252590.1|2581805_2582336_-|GIY-YIG-nuclease-family-protein
MIIGAYGLFWEQGLVEWDARPWRLLGRRGLNSGSLRIVDFRRARGVYILYNDVNVYYVGLAVGANGIGSRIRDHLDDEHSQLWNRFSWFTFDSPDGEGAIGDDGVETVTQTYNGVENLDTKDLIRDLEALLQQAMQPLANKAMTKFADGEEWYQVASRVPEVLLFEHLAPRLRPRL
>NZ_CP051626.1|WP_169252589.1|2581096_2581789_-|hypothetical-protein
MADIDSAFPEVSSDTIDFAKSKCLLVLRDDLTPGRVRRYYDANTNYAGSTFAGLEPNVSDTITATDLLAVTTLSVDIPVLAVRRILEDEATQNELRVALGSLPTCSLEDTVEHDFPAMQVFYDLVKSLLARADTKSSNAWVTASKITARKRPGLFPVRDNVVCKLLGIDRLGDRAKDWIVFRELMRDKEVRAALTATVSKAEALKDERVVRFDVQPLRQLDVALWTAESK
>NZ_CP051626.1|WP_169253889.1|2578251_2580675_-|aminodeoxychorismate-synthase-component-I
MRTLLIDNADSFTLNLFHLLAEVNECAPTLVPNDWTEFELSVLDEFDNVVISPGPGTPERSADFGICAEVIEHSTIPVLGVCLGHQGIAHVHGGAVVHSPEPRHGRVSAIRHTETELFAGIPSPFSAVRYHSLAVTDLPDCLEATAWSEDGVIQALRHRSRPQWGVQFHPESIASDEARTLLRKFAELTAAWNRGTEHQDDGSVNEAWDGEEIVSKSDLLAGTCAALNRSEATPHPADDRHHYILDTDVLPQTFTDERLFAELFGDEPEAVWLDGNLPGNDSSRFSIMGAPSGPLSKVATASVSEGTVEVRSASGESKSFIQSSGFFDWLDIELASTTVSVSGTEDEPPSAGSETPDIRADNHDLPFDFHLGWVGYLGYELKTEVGSPNQRESDLPDAVMMFLDRALIIDHETERIHLLVLRRDDDPAGRATNQEWLDYTRTRIASIPTDEVTGAHQPSTASAKADITNPAKRRDPNLVARNSRHEYLDLIDQVQEKITDGETYEVCLTNMLEGTVDPHASPLEMYLRLREDNPTSFGAFIRTREAVILSTSPERFLRIGADGRVESKPIKGTRPRGATPAEDEAIKAELAASVKDRSENLMIVDLVRHDLGRTAELGSVQVDTLFGIESYATVHQMVSTVSSRLAEDASPVACVRAAFPPGSMTGAPKLRTMTTIEELEAGPRGVYSGAVGYFSLGGAVDLSVVIRTLVVQGETLSYGVGGAIVALSDSEEEYEETVVKAAPVLRLLGGVEFPGEVVVHANAPSELRTHIHSTEQIGDADVHTMIPAEEAGPTDTAVAEYSGGVER
>NZ_CP051626.1|WP_169252588.1|2577400_2578255_-|aminotransferase-class-IV
MNVWLWNQQDHRFEEPTTDISSSKLMAADSWLVEDGRVRAFDLHRTRFGDAAAQVGMGDAITDEFWAAVVEKISAKGEWFPRVDVLDVSPDAERELAFRLRPAPTRTQELKVLIPPYSDPRITPNRKGPDIALLERVREEAGEQYSCDEVLLINGDGYVIEGATTSLLWWDEETLCAQDPELGALPGVTSAVILEEARARSVPIELRRVRPEELMEHEAWLVNALHGIRRVSELVDGRDLHDSVQRGDEPNQIWAGHRGGPHADAVRLGRWREWLETIRVAPGM
>NZ_CP051626.1|WP_062861908.1|2576013_2576325_+|hypothetical-protein
MSTPASLPYAFVAKIVAADGQHDAVADLLAGAVALANEEVGTIVWFAVRTDADTFWIFDAFPDEAARDAHANGAIVAALMANQHLLSAAPEILAADVLASKLP
>NZ_CP051626.1|WP_169252587.1|2574964_2575906_-|helix-turn-helix-domain-containing-protein
MRIGLIAIDGCFGSAIASIIDIVRVADGARGDVDPRIDPIELAILGPKRRVATTASMTLSVDHPLSESAEFDVVIVPALGTLTAAATNDALQSRDARSVIASLGRLDEATTRIAAACTGVFAVAETGRMHHRRATTSWFLGPEFLKRYPTVALDLDTMVVADGNLVTAGAAFAHIDLALSLVRSISPDLAQHVAKLLIIDERPSQAAFVAYEHLRHEDPIVVEFERFVRARLDEPFNVAFVAQSLGTSRRTLERRVRAALNLTPLGFVQRLRIERARHLSATTDLTSAEIALRVGYANAETLRSLLRRERRRS
>NZ_CP051626.1|WP_169252586.1|2573885_2574599_+|amino-acid-racemase
MRRIGLLGGMSWHSSIEYYTKINDAVAKKLGGHHSAQILLDSCDFADIRELQEANDWAGNDASLTATAKRLVDGGAEAVAIATNLMHKCAPAIEASVDAPFIHMVDSIATMAKRQGYSTLAVLGTRWTMLEDFYTGRLEAQGIKTLVPDEETCLEVDQIIWDELTQGIFTDKSGARYVEIMNDLKARGADAVALSCTEIGLLVPPETAPLPALDSVDAHVSAIVEWIMADEPVTIRH
>NZ_CP051626.1|WP_169252594.1|2587425_2589060_+|acetolactate-synthase-large-subunit
MTTQRASDVMVRALENEGVERIFGIPGEENLDFVDSLRNSSIELILTRHEQAAAFMAATYGRLTGKPGVVLTTLGPGALNLATGAAYAHLGGMPVIMITGQKGIRTAEQAAFQMVNTVATMDPLTKVSKQISSAAMIPTMVREAFRAAQAERPGPVHLELPEDIAGMPVDGFELIEPHTNSRPVAGDTAIANAANVIREAKNPLLMLGADASRASCSEALSRFVAGMRIPYVTTQMGKGSVTGASDLYMGTAALTSGDYVHDAIDAADVIVTIGHDTTEKPPFTMDENGPTVVHIGYRPAIVEQVYFPQFEVIGDLAPSLDKLAEVLDGPVPTAEALLPMRDEILIKIHEGADEDRFIPQRIVQEVRDVVPTDGIVALDNGMYKIWFARNYRTTRANTLLLDNALATMGAGLPSAIGAKLTYPERRVMAVVGDGGFMMNSQEMETAVRLGLDLVVVILEDNAYGMIRWKQAADGMADFGLTFDNPDFVKYAESYGATGTRVKDVDSISDALEHAFSVGGVHIVVVPVDYSENKRVLIDELGQRS
>NZ_CP051626.1|WP_169252595.1|2589093_2590188_+|MerR-family-transcriptional-regulator
MTVSDLMPIGTFARIVGLTASALRFYDDAGVLRPDHVDAQTEYRFYSDAQVAAAQRLRELRELGMPLSDVSRFFAAESASDSTESLRLLNDHLRRVSAENARLQHVAARLSESLQSEASTSLCTLSGPVFAAAVDQLLATTADDPDFPVLNGVRLSIEPDALTLAATDRYRFTSRTLVPSRSAGTTWAGTVSGHALRTAVSAIRRSPTVTLEAGDDVLRVVLDDGTMSQCTLIDEPFPDTSDFFSSLPTAVHHCMVDRRQLLQTMERQAPDKVGLRLSASGVRVLHPADSVDIDGTGDGSELTLWFELTTLHPAVANALGNDLILDVTASDQPVVLRSADDGDFTTVLMPCQAPPTDTDRNRPP
>NZ_CP051626.1|WP_169252596.1|2590242_2590716_+|hypothetical-protein
METIGRAVELGRSGDVGTAQRQLVSLWQEVGPTGDPFHHCTLAHYLADLLDHPAEALIWDIRALDAAASLSDERAQAHHQSLQVAGFYPSLHLNIADNFRCLSAFGAAAEHICAAEERSEALPDDGYGRMIRTAIDEVRAAIDRRETARRDSAPGGS
>NZ_CP051626.1|WP_169252597.1|2590737_2591397_-|pentapeptide-repeat-containing-protein
MVTSAPRPPKLSLGDLVPGYLGDFGPEEFLEGMEFTDLDLAEADATQATFLDCRMTNVNFGDAEAQIDLSGVRISGTEITDCRADTWTIPRGNLLHTDVSGTRIGAGVAYDSVWEKVRFTNCRISYLNLRESKLTDVEFRDCKIDEIDLDRAKASRVAFPGSSVGVFQCEGATLGNVDIRGLEPHKISGVHSLRGAIIDDTQLMLFAELFASELGISVE
>NZ_CP051626.1|WP_169252598.1|2591859_2592978_+|nucleotide-binding-protein
MTDRSAEFIAIAEEASEIADRESSLDTQPLDALENAAKEIGRSWSKSNLGYQANVYYQGFEAPPNGAMFSREWGLLGMFQGTTGEWEIHQVDEVVAKIEERAGNPDLNRLREQSDATGSEVEELIQRARSVAAKVPIPCDDYVKENVEELQHIILPDADSLARLQMRGVTGQIMTRDAQALEGGAQPAGHQIALATVRKLKSPFLVARELATVCKRLGKHLEGDEATTQRAVIQLGSKVFIGHGGASAEYLKLGVWLSGQGLGWEVFDRKPTAGMSVKERLLEMLDNASIAFLVMTPEDENSEGKAVARANVIHEVGLFQGRLGWMKAIVLLEEGCEEFSNIEGIGQIRYPKGNIKAAFDEIRQVLHREGVI
>NZ_CP051626.1|WP_169252599.1|2594075_2595101_-|AsnC-family-transcriptional-regulator
MIVMVRNDTMARLHPHRPRAGKSGESAVLDEVDRKIVAALQVAPRASWARVANVLELSESVVFRRGKKLLDSEVVQVSALPDPTLTDRGFPVLVRLRCEVGEAYSVARAMAARPDTRLVLALAASYDVLVELIVPTRHSLGDVLQEGFKDVSGIVESESATVIRNFKTSFDWARASVGSDLSQLDEKRACSELNRTVDESDLKIIEILAGNGRLSYKTVGEIAGLSESSVRRRVDALLDNGAFQFATYVEPDLLGFNAPLFVWFDVDARDLEGVAARLSALPEVRYVSATTGKSQLAAEILSRGIDDIYDLTTSEILGVDDVKRVDVGLEVRSFKRGFMIR
>NZ_CP051626.1|WP_169253890.1|2595323_2596550_+|diguanylate-cyclase
MISHDKKESVFELKKYGGYKSYEYLEAGVDYIDFKLAPEFDRAPKHDLDLDDVEAQRTAQLLRDNIVISLHDHPTVFPEDMSETRAYNRTGRQRTGYAGLAKSGMTVVFDNMMDGTACVTSKFGWKFDDVIYDLGMRLSDIAHQDFVTLCRNAEDINQAHETGNVTLVMSLEAATPIENELDRLDILYGLGIRSMGIAYSESNALGSGLKEPGDGGLTMFGRQAVKRMNQLGIAIDVSHSSDQTCLDTIEHSEAPVLITHAGARAIWPTKRMKPDEVLKACAESGGVIGLEAAPHTSLSHDHIEHSIDSVMDHFEYCVELMGIDHVSFGPDTLYGDHVGLHDEFASNLGVHNATAAPDYPKMPYVSGMENPTECFFNIVGWLVKHGYSDEDIVKVISSNTLRALNFIW
>NZ_CP051626.1|WP_169252600.1|2596763_2597099_+|alcohol-dehydrogenase-catalytic-domain-containing-protein
MGADTSGTVVYVGKTANTDLQVGEPVVIYPGLSCDACARCRSGDTTMCGHYKLMGEDVDGVQGAVSHKLRYISLSLPGRRSSLGPVIAVRPSSVSPRWEPRSWSTLQIPIG
>NZ_CP051626.1|WP_169252601.1|2597053_2597458_+|zinc-binding-dehydrogenase
MGAEIVVDTSNPDWVSELAVFTQGRGVDVVVDPIGAATWKRSINALSTGGRLATCGAATGDSVEISIREIYQHHRSIVGAPMNGIRQFHAATRMVSTKRLKPTVDSTYSFGSVQRAHQRLSPSEGFGRIVLAVD
>NZ_CP051626.1|WP_169252602.1|2597701_2599147_+|sodium/solute-symporter
MSFTTVFIIVFAIFVIVVLIEGLRSAKSQSGEKDFLVAGRGMGAWVGGASIAATQMSAGTFVGTMGIHYLTGSSFLMPTIGIWLAFIFAGFVIAPRLHRYIDKTGALTFPDFIGDRYGQKLPRVVITVLLIGSYLIFLSAQYQAGGIVFQQIFDIPFYWGSTILMVFIVIYTVVGGMTAVMRTDFVQQIVMSLAVVIGVPVAIHAAGGIGELPTEFNDIGAEFAGWNYSWVDLLGFVMGFGFAAMVAPVLLMRFYAMRDAKTCARGSLVAVFFTMITFGCVAIIGMSMRIISPDLESPDLASSVFATEVLPSFLGALMLTAVLAAVLSTVDSVLLVIGPAFSHDLYGKILRPQATERQRLRTARIATIVFGALPILLTFMQLDVVQFIVLAYAALVGSTVFAPLVLGIFWERANTAGAMTAMVGGFSVCLIWYLIGQPYFAPVVPGIIVNVLAMAIVSPLTKRPEPQTLEPFFDQPDKVRT

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Crispr_ID: NZ_CP051626_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051626_4

3514535-3514634

Orphan

Consensus_repeat	Method
CCCCCGCCGAGGCGGCCGGGCCGTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051626_4

>merge|NZ_CP051626|4|3514535-3514634|CRISPRCasFinder
CCCCCGCCGAGGCGGCCGGGCCGTTGCCTGCGGGAGCAGCGTGGTGTGCATGACCGGTGTTGCCGACGCCGGCATCCCCCGCCGAGGCGGTCGGGCCGTT

>NZ_CP051626|4|4|3514535-3514634|CRISPRCasFinder
CCCCCGCCGAGGCGGCCGGGCCGTT	GCCTGCGGGAGCAGCGTGGTGTGCATGACCGGTGTTGCCGACGCCGGCAT
CCCCCGCCGAGGCGGTCGGGCCGTT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051626.1\|WP_101554655.1\|3511594_3511990_-\|universal-stress-protein	unknown	unknown	gnl\|CDD\|366180
NZ_CP051626.1\|WP_169253260.1\|3525752_3527825_-\|TRAP-transporter-permease	unknown	unknown	gnl\|CDD\|273983
NZ_CP051626.1\|WP_169253257.1\|3519832_3521488_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224048
NZ_CP051626.1\|WP_169253977.1\|3512286_3513648_-\|APC-family-permease	unknown	unknown	gnl\|CDD\|129987
NZ_CP051626.1\|WP_169253978.1\|3522398_3523391_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223674
NZ_CP051626.1\|WP_169253250.1\|3510411_3511497_+\|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|223566
NZ_CP051626.1\|WP_169253246.1\|3500666_3503753_+\|aminopeptidase-N	unknown	unknown	gnl\|CDD\|341065
NZ_CP051626.1\|WP_169253258.1\|3521487_3522399_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224094
NZ_CP051626.1\|WP_169253251.1\|3512074_3512284_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|240609
NZ_CP051626.1\|WP_169253252.1\|3513825_3514527_-\|type-1-glutamine-amidotransferase	unknown	unknown	gnl\|CDD\|153212
NZ_CP051626.1\|WP_169253255.1\|3517825_3518626_-\|serine-hydrolase	unknown	unknown	gnl\|CDD\|379138
NZ_CP051626.1\|WP_169253256.1\|3518622_3519840_-\|LD-carboxypeptidase	unknown	unknown	gnl\|CDD\|132882
NZ_CP051626.1\|WP_169253248.1\|3505584_3506700_-\|LLM-class-flavin-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|274646
NZ_CP051626.1\|WP_035321156.1\|3517402_3517711_-\|DUF3870-domain-containing-protein	unknown	unknown	gnl\|CDD\|372419
NZ_CP051626.1\|WP_169253249.1\|3506858_3509165_-\|DUF222-domain-containing-protein	unknown	unknown	gnl\|CDD\|238038
NZ_CP051626.1\|WP_169253254.1\|3515997_3517155_-\|DUF819-domain-containing-protein	unknown	unknown	gnl\|CDD\|227792
NZ_CP051626.1\|WP_169253259.1\|3523633_3525466_-\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|173853
NZ_CP051626.1\|WP_169253247.1\|3504123_3505212_-\|C40-family-peptidase	unknown	unknown	gnl\|CDD\|366353
NZ_CP051626.1\|WP_025780412.1\|3509573_3510173_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|238045
NZ_CP051626.1\|WP_169253261.1\|3527821_3528805_-\|TAXI-family-TRAP-transporter-solute-binding-subunit	unknown	unknown	gnl\|CDD\|270285

Protein	Function_ID	Function_description	E-value
NZ_CP051626.1\|WP_101554655.1\|3511594_3511990_-\|universal-stress-protein	gnl\|CDD\|366180	pfam00582, Usp, Universal stress protein family. The universal stress protein UspA is a small cytoplasmic bacterial protein whose expression is enhanced when the cell is exposed to stress agents. UspA enhances the rate of cell survival during prolonged exposure to such conditions, and may provide a general "stress endurance" activity. The crystal structure of Haemophilus influenzae UspA reveals an alpha/beta fold similar to that of the Methanococcus jannaschii MJ0577 protein, which binds ATP, though UspA lacks ATP-binding activity.	3.35038e-17
NZ_CP051626.1\|WP_169253260.1\|3525752_3527825_-\|TRAP-transporter-permease	gnl\|CDD\|273983	TIGR02123, conserved_inner_membrane_protein, TRAP transporter, 4TM/12TM fusion protein. In some species, the 12-transmembrane spanning and 4-transmembrane spanning components of tripartite ATP-independent periplasmic (TRAP)-type transporters are fused. This model describes such transporters, found in the Archaea and in Bacteria. [Transport and binding proteins, Unknown substrate].	0
NZ_CP051626.1\|WP_169253257.1\|3519832_3521488_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224048	COG1123, COG1123, ATPase components of various ABC-type transport systems, contain duplicated ATPase [General function prediction only].	0
NZ_CP051626.1\|WP_169253977.1\|3512286_3513648_-\|APC-family-permease	gnl\|CDD\|129987	TIGR00909, putative_amino_acid_transporter, amino acid transporter. [Transport and binding proteins, Amino acids, peptides and amines].	1.27864e-34
NZ_CP051626.1\|WP_169253978.1\|3522398_3523391_-\|ABC-transporter-permease	gnl\|CDD\|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	2.41228e-117
NZ_CP051626.1\|WP_169253250.1\|3510411_3511497_+\|NAD(P)/FAD-dependent-oxidoreductase	gnl\|CDD\|223566	COG0492, TrxB, Thioredoxin reductase [Posttranslational modification, protein turnover, chaperones].	2.13391e-44
NZ_CP051626.1\|WP_169253246.1\|3500666_3503753_+\|aminopeptidase-N	gnl\|CDD\|341065	cd09602, M1_APN, Peptidase M1 family including aminopeptidase N catalytic domain. This model represents the catalytic domain of bacterial and eukaryotic aminopeptidase N (APN; CD13; alanyl aminopeptidase; EC 3.4.11.2), a type II integral membrane protease belonging to the M1 gluzincin family. APN preferentially cleaves neutral amino acids from the N-terminus of oligopeptides and, in higher eukaryotes, is present in a variety of human tissues and cell types (leukocyte, fibroblast, endothelial and epithelial cells). APN expression is dysregulated in inflammatory diseases such as chronic pain, rheumatoid arthritis, multiple sclerosis, systemic sclerosis, systemic lupus erythematosus, polymyositis/dermatomyosytis and pulmonary sarcoidosis, and is enhanced in tumor cells such as melanoma, renal, prostate, pancreas, colon, gastric and thyroid cancers. It is predominantly expressed on stem cells and on cells of the granulocytic and monocytic lineages at distinct stages of differentiation, thus considered a marker of differentiation. Thus, APN inhibition may lead to the development of anti-cancer and anti-inflammatory drugs. APNs are also present in many pathogenic bacteria and represent potential drug targets. Some APNs have been used commercially, such as one from Lactococcus lactis used in the food industry. APN also serves as a receptor for coronaviruses, although the virus receptor interaction site seems to be distinct from the enzymatic site and aminopeptidase activity is not necessary for viral infection. APNs have also been extensively studied as putative Cry toxin receptors. Cry1 proteins are pore-forming toxins that bind to the midgut epithelial cell membrane of susceptible insect larvae, causing extensive damage. Several different toxins, including Cry1Aa, Cry1Ab, Cry1Ac, Cry1Ba, Cry1Ca and Cry1Fa, have been shown to bind to APNs; however, a direct role of APN in cytotoxicity has been yet to be firmly established.	0
NZ_CP051626.1\|WP_169253258.1\|3521487_3522399_-\|ABC-transporter-permease	gnl\|CDD\|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.18383e-87
NZ_CP051626.1\|WP_169253251.1\|3512074_3512284_+\|hypothetical-protein	gnl\|CDD\|240609	cd12796, LbR_Ice_bind, Ice-binding protein, left-handed beta-roll. The ice-binding protein of the grass Lolium perenne (LpIBP) discourages the recrystallization of ice. Ice-binding proteins produced by organisms to prevent the growing of ice are termed to anti-freeze proteins. LpIBP consists of an unusual left-handed beta roll. Ice-binding is mediated by a flat beta-sheet on one side of the helix.	2.42177e-05
NZ_CP051626.1\|WP_169253252.1\|3513825_3514527_-\|type-1-glutamine-amidotransferase	gnl\|CDD\|153212	cd01741, GATase1_1, Subgroup of proteins having the Type 1 glutamine amidotransferase (GATase1) domain. This group contains a subgroup of proteins having the Type 1 glutamine amidotransferase (GATase1) domain. GATase activity catalyses the transfer of ammonia from the amide side chain of glutamine to an acceptor substrate. Glutamine amidotransferases (GATase) includes the triad family of amidotransferases which have a conserved Cys-His-Glu catalytic triad in the glutaminase active site. In this subgroup this triad is conserved. GATase activity can be found in a range of biosynthetic enzymes, including: glutamine amidotransferase, formylglycinamide ribonucleotide, GMP synthetase , anthranilate synthase component II, glutamine-dependent carbamoyl phosphate synthase, cytidine triphosphate synthetase, gamma-glutamyl hydrolase, imidazole glycerol phosphate synthase and, cobyric acid synthase. Glutamine amidotransferase (GATase) domains can occur either as single polypeptides, as in glutamine amidotransferases, or as domains in a much larger multifunctional synthase protein, such as CPSase.	7.41257e-54
NZ_CP051626.1\|WP_169253255.1\|3517825_3518626_-\|serine-hydrolase	gnl\|CDD\|379138	pfam13354, Beta-lactamase2, Beta-lactamase enzyme family. This family is closely related to Beta-lactamase, pfam00144, the serine beta-lactamase-like superfamily, which contains the distantly related pfam00905 and PF00768 D-alanyl-D-alanine carboxypeptidase.	3.51402e-36
NZ_CP051626.1\|WP_169253256.1\|3518622_3519840_-\|LD-carboxypeptidase	gnl\|CDD\|132882	cd07025, Peptidase_S66, LD-Carboxypeptidase, a serine protease, includes microcin C7 self immunity protein. LD-carboxypeptidase (Muramoyltetrapeptide carboxypeptidase; EC 3.4.17.13; Merops family S66; initially described as Carboxypeptidase II) family also includes the microcin c7 self-immunity protein (MccF) as well as uncharacterized proteins including hypothetical proteins. LD-carboxypeptidase hydrolyzes the amide bond that links the dibasic amino acids to C-terminal D-amino acids. The physiological substrates of LD-carboxypeptidase are tetrapeptide fragments (such as UDP-MurNAc-tetrapeptides) that are produced when bacterial cell walls are degraded; they contain an L-configured residue (L-lysine or meso-diaminopimelic acid residue) as the penultimate residue and D-alanine as the ultimate residue. A possible role of LD-carboxypeptidase is in peptidoglycan recycling whereby the resulting tripeptide (precursor for murein synthesis) can be reconverted into peptidoglycan by attachment of preformed D-Ala-D-Ala dipeptides. Some enzymes possessing LD-carboxypeptidase activity also act as LD-transpeptidase by replacing the terminal D-Ala with another D-amino acid. MccF contributes to self-immunity towards microcin C7 (MccC7), a ribosomally encoded peptide antibiotic that contains a phosphoramidate linkage to adenosine monophosphate at its C-terminus. Its possible biological role is to defend producer cells against exogenous microcin from re-entering after having been exported. It is suggested that MccF is involved in microcin degradation or sequestration in the periplasm.	1.77763e-78
NZ_CP051626.1\|WP_169253248.1\|3505584_3506700_-\|LLM-class-flavin-dependent-oxidoreductase	gnl\|CDD\|274646	TIGR03558, oxido_grp_1, luciferase family oxidoreductase, group 1. The Pfam domain family pfam00296 is named for luciferase-like monooxygenases, but the family also contains several coenzyme F420-dependent enzymes. This protein family represents a well-resolved clade within family pfam00296 and shows no restriction to coenzyme F420-positive species, unlike some other clades within pfam00296. [Unknown function, Enzymes of unknown specificity].	9.73206e-116
NZ_CP051626.1\|WP_035321156.1\|3517402_3517711_-\|DUF3870-domain-containing-protein	gnl\|CDD\|372419	pfam12986, DUF3870, Domain of unknown function (DUF3870). A family based on the C-terminal domain of 3KOG which shows structural similarity to pore-forming proteins, suggesting it may have a lytic function.	1.18193e-36
NZ_CP051626.1\|WP_169253249.1\|3506858_3509165_-\|DUF222-domain-containing-protein	gnl\|CDD\|238038	cd00085, HNHc, HNH nucleases; HNH endonuclease signature which is found in viral, prokaryotic, and eukaryotic proteins. The alignment includes members of the large group of homing endonucleases, yeast intron 1 protein, MutS, as well as bacterial colicins, pyocins, and anaredoxins.	3.80191e-12
NZ_CP051626.1\|WP_169253254.1\|3515997_3517155_-\|DUF819-domain-containing-protein	gnl\|CDD\|227792	COG5505, COG5505, Predicted integral membrane protein [Function unknown].	1.66873e-94
NZ_CP051626.1\|WP_169253259.1\|3523633_3525466_-\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|173853	cd00995, PBP2_NikA_DppA_OppA_like, The substrate-binding domain of an ABC-type nickel/oligopeptide-like import system contains the type 2 periplasmic binding fold. This family represents the periplasmic substrate-binding domain of nickel/dipeptide/oligopeptide transport systems, which function in the import of nickel and peptides, and other closely related proteins. The oligopeptide-binding protein OppA is a periplasmic component of an ATP-binding cassette (ABC) transport system OppABCDEF consisting of five subunits: two homologous integral membrane proteins OppB and OppF that form the translocation pore; two homologous nucleotide-binding domains OppD and OppF that drive the transport process through binding and hydrolysis of ATP; and the substrate-binding protein or receptor OppA that determines the substrate specificity of the transport system. The dipeptide (DppA) and oligopeptide (OppA) binding proteins differ in several ways. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Similar to the ABC-type dipeptide and oligopeptide import systems, nickel transporter is comprised of five subunits NikABCDE: the two pore-forming integral inner membrane proteins NikB and NikC; the two inner membrane-associated proteins with ATPase activity NikD and NikE; and the periplasmic nickel binding NikA, which is the initial nickel receptor that controls the chemotactic response away from nickel. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand binding domains of ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	1.50002e-124
NZ_CP051626.1\|WP_169253247.1\|3504123_3505212_-\|C40-family-peptidase	gnl\|CDD\|366353	pfam00877, NLPC_P60, NlpC/P60 family. The function of this domain is unknown. It is found in several lipoproteins.	2.76539e-31
NZ_CP051626.1\|WP_025780412.1\|3509573_3510173_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	7.60436e-17
NZ_CP051626.1\|WP_169253261.1\|3527821_3528805_-\|TAXI-family-TRAP-transporter-solute-binding-subunit	gnl\|CDD\|270285	cd13567, PBP2_TtGluBP, Substrate binding domain of Thermus thermophilus GluBP (TtGluBP) of TAXI family of the tripartite ATP-independent periplasmic transporters; contains the type 2 periplasmic binding protein fold. This subgroup includes TtGluBP of TAXI-TRAP family and closely related proteins. TRAP transporters are comprised of an SBP (substrate-binding protein) and two unequally sized integral membrane components. Although TtGluBP is predicted to be an L-glutamate and/or an L-glutamine-binding protein, the substrate spectrum of TAXI proteins remains to be defined. A sequence-homology search also shows that TtGluBP shares low sequence homology with putative immunogenic proteins of uncharacterized function.	4.86107e-97

>NZ_CP051626.1|WP_169253252.1|3513825_3514527_-|type-1-glutamine-amidotransferase
MTRLLVIVNDIDSQPGLLTRWMISENVEFDLRIGGVSPLPGPAELDAYDGLIMLGGGYMPDETDRAPWLADEAALVRRALELDLPQFGICLGGQLIAHVIGGDVRAQTGAPEKGYTQIDTTAEAAADPVFSAIRPRTSFVESHVDRIVALPEEASLLATSAACEFQAFRVGQAWGTQFHPESTRVNIERWDAEKLQTLGFDKDTLLEEAKELGPESERDSQALFSAFLTVVRN
>NZ_CP051626.1|WP_169253977.1|3512286_3513648_-|APC-family-permease
MGPKLLLLFIVGDILGTGVYALTGKVAGQVGGAGWAPVILAFLIALITAFSYMELVTKYPQAAGAALYTHKAFGVHFVTFLVAFAVLSSGITSASTASNVFAANLVAGFGWDVSGTGVMWIALAFLTLIALINLRGVGESVWFNVVLTLIELSGLLLVIVVGFFALGAGDADFSRVMIFETEGDKSVFLAVTGATALAFFSMVGFEDSVNMVEETKDPRIFPKIMLSGLTITGIIYVLVSLVTVAAVPIGVLTESETPLLEVVREGAPGLPIDTIFPFMTMFAVANSALINMLMASRLLYGMAKQNVLPPVFAKVLAGRRSPWVSIIFTTLIAFALIFFVTSILPETVTASLGGTTSLLLLAVFAVVNVAVLILRKDKSGNAEHFKAPTVLPWIGVITCVFLVGPWARLDELIQYQIAAALVGIGVVLWAVTWFWNRSTKGTSTRFRNPEELT
>NZ_CP051626.1|WP_169253251.1|3512074_3512284_+|hypothetical-protein
MARWVIPSAPELRCTSARDGRAASARERTDAAKNGTVPGKNDTVPGKGGTVPGKGGTVPGRDGTASARG
>NZ_CP051626.1|WP_101554655.1|3511594_3511990_-|universal-stress-protein
MTVLVGYVNNPAGHAALDAGIAQAKKDGKELVVVNASRSAQRNDSYRLGEGELRSVNDYLTRADVEFRVLTSGSEYDPAEQILDTATEVGAELIVLGTRKRTPVGKFLLGSTIQKVILDATAPVLCVKAAH
>NZ_CP051626.1|WP_169253250.1|3510411_3511497_+|NAD(P)/FAD-dependent-oxidoreductase
MTAPSTPEYSRPSASEGSRPSSSEGSRPSPSETLASSAESAQNSFDVAVIGGGAGGLAASIALARSLRSVVVIDAGQLRNSSSPHAHNVLGHEGIRPQDLVAKGRAEAAEYGVAFIDATVQNARTIDSDPNSAEAAPRHRFELTTSAGVDVRARRIIIATGLSDELPDVPGLAEGWGDTVLHCPYCHGYEVRGQRIGVIGTTAMSYHQAMLFSQLSDRVSFIRHAAPAPDSEQAAMLETLGIEYIDSTVTEVARTDSDTVVSLTADESADGANARTFDALAVGAYARANAELFAQLGGEVVAHPSGMGTYIPTQMAGQTDVPGVWAVGNSADVSAMVVASTASGVLAGAHVNADLIMERLG
>NZ_CP051626.1|WP_025780412.1|3509573_3510173_-|helix-turn-helix-transcriptional-regulator
MLADGAAPVEAQEAIRQSLAGVGARLRSLRQEQNRTLDEVAELAGMSTSTLSRLESGKRKPSLELLLPLAGVYGLPLDELVGTPPIGDPRIHISPRKFHDQTILPLSRGAIGVQAFKHIVDGRQTPKLGALKTHPGFEWVYVIRGRLTLILGDRTMILSAGEAAEFDTRTPHWFGGADDDGVEYLSLFGPEGQRVHMKS
>NZ_CP051626.1|WP_169253249.1|3506858_3509165_-|DUF222-domain-containing-protein
MALIPDRRYDEHSEREAGKASQAPPPQGSPPSGLPPTAAGSSVCSADGDSSRSTYRELLAEAGFDLTGHPLADRFDAIADNLVDGEAGAEVSTAVERVAAVEGVAAVEGVAAVEGVAAVEGGSQPAAVEGDADDSPLPGGDIRAGQGLWTSRTTMPETEAEVQACIKEIEARQSAWMKVKREEREAQKAAEREEFLRKNPQARAEDEELARERAEWNARVERYEAKKRAQEEAERIAEAERTERHKALAEHYDSEADAHPLLDEFRWSDLKHAAPEVAESICALQGLLDGLHDFTRPMGPDDAVTLLDGLETLNRLTESLSIVTLSVFERVGTPRDYGAKTTKALVQHRLNLSAHEAQRRTQLAECLGKRTSISGESIEAQFPILAAALREGVLSANQASTISKCLKNLPVNVSEDDKIKAESLLVEKAQAVRVCDIHALFEEILGWIDPDGQEPKEAADRDSFAVNLRQAKDGTWTLKGRLDEETGGILNGLLTSRIKTDSPSDDEGCDDTAASGADRDREIVDTFSEVLRGDRSDCLDPSLDFAPPQVGENGEIPQGAGVKQDGTLVAMAAEQPSVRRRIYERFSSVIGSIEMNRIKAGAAYALVVTAKAEDVANQTGKAVTGVEAPFPIDAAVLEGLNGSVFFHLMGEKAKSMALATERRLATEKQLAILASRDQGCTFPGCDTPPGWCEAHHIVPWAENGKTDVNNLTLACSAHHHLLDYTEWDCRMLIDGRPAWVPPATIDPAQEPVLHARFIAREIGETLFG
>NZ_CP051626.1|WP_169253248.1|3505584_3506700_-|LLM-class-flavin-dependent-oxidoreductase
MKLSILDLIPVRTGQTTADSFAASKQIIDTADKLGFTRYWVAEHHNMPSIASTMPGPELMYLGQGTQQIRLGSGGVMLPNHAPLAVAELFALLSAVYGDRIDLGIGRAPGTDPITSAAMRGHLGEGRMVDGEGRAIDPVEQFPQHVIDTLSLMQPEGMRVPLHGGREHVLKATPAAVPGTQPLPWLLGSSGYSARLAAELGMPYVFANHFASGATTGMKIYRDNFTPGAYGDTPQTFVTANVVAAPTEDEAQLRSEPFMLQMARLRTGGPMEKLHLAGDDVRSVMTDQERMVGEELSGNWIIGDTESVSAQLEELAERFDVDEIMIQPIAGAMEGEDVREDPGRIQTIELLAAEVLGSTTASGVAGAGTDK
>NZ_CP051626.1|WP_169253247.1|3504123_3505212_-|C40-family-peptidase
MRTKIAVSAALGVGLVFGAGAPALSSNLSSTDAANTSGISAGVVPGQELERITDGKIEKGETAYVDVTVATLWTDPKAPRKVDKPALQHPVDLKKWNKNLESTDVRRGLTGKTETQATYGSEVSVLDIKGSWAKVAVTDQKTPKDKKGYPGWLPKKQLVENDRFGKLREDQPRAVVTKPKSELEGIEFTKDTGADVSFNVDLPLIAQDVDDVRVALPGGGAAWIDIDDVEVYDVGGKPEKPSGKDLVKTAKQFDGLRYLWAGVSAYGFDCSGFTYSIYKAHGIDLPRDSGEQAKAGKAVSSSNLKPGDLLFFSTSSGTVHHVGMYVGDGKMIHSPNASKDVYVTDWKKWDSGNEFSGARRIL
>NZ_CP051626.1|WP_169253246.1|3500666_3503753_+|aminopeptidase-N
MTTNLTRSEAQSRTQLLEVDSYSVHIDVSNAETDADTYLSRTVVDFTARFVDSTFIDLIADSVTSVLINGESLSPAEVFDGARVTFPVRAGRNSLTIEAQARYSTSGEGLHRFTDPADGKTYLYTQYEPTDARRVFANFDQPDLKAEFIFTVTAPAHFQVLSNRAEARTEPAEAAAGAASAVTHHFEPTLKQSSYITCITAGPYEGATDEWTDPRTGQTVQLGAWTRASLVDHLDADDIFGVTKAGLDFFTSEFDYPYPWGKYDQIFVPEYNLGAMENPGLVTFTDNLIFRDKVTDANYESRANVILHEMAHMWFGDLVTMKWWDDLWLKESFADFMGGLALAEATRFTDGWVTFALRRKAWAYTQDLYPTTHPIVADIPDVEAAKLNFDGITYAKGASVLKQLVAFVGREAFFAGSRLYFKRFEYGNTELADFLECLAEAAPDRDIANWAAAWLGTSGVSELSLQLTTSDGAAGPSAGSAAGSAGAVGSAGAVGSAGYSGSAGFASGGAPTDSVAASRGAGGGRLVASSSGARLRSPDAVDDSVDSATGVAHAAGSGGSGSVQPPRRRSGSEKVTGATITQADSAEGAALLRPHTIEIATLGRSGRAIVPLDSFRFEFSTESADVEQLIGRSAGVITLLNYNDLDYARVRLDPESMEAAVTSASRITDPLSRALVWSALDNAVRDGLMPVQKYLTAYARSLGKESHAGIMAGLSQTALTCIDQWVADRNFDAAIMGLLGAALDALAAAKAGSDAQLHLANLVLALTSRTARCAAGSSAVAMGRGFASQILAVPVGEEVDRMYAGAPGQAGRVDSADQAEAVDQAGTVDQSVEASGGARAGRGAEHSTATLPFRGLINDHALRWNALTALVCLGWADQTDIARENHSDPSSSGRLHAETASAALPLPIVKIRAWEAIREAGALSNDVLSAIISGFIAPSAMPLIEEYVDEYFDGLLGFWMDNSIEIARRLVLGLYPRWSVNEEAVVEKTDAWLAANVDAPAALRRLVIERRDDLARAIFLKSTQSSRH
>NZ_CP051626.1|WP_169253254.1|3515997_3517155_-|DUF819-domain-containing-protein
MITDGFLFISLLLAISAALVVADRSGRFKLFKYVPGFVILYIVAALLNTFGVFDHDGGDITAVGDTLREVMLPAMILLMLFKCDVRQIIKLGPKLLLTFAVTAASIIAGFIISYLILHSSLDPEAWKALGALNASWTGGSANMVAVQEVLQAPENVFGYVLIVDTVLYSFWLLLVFSSVTVSDKFDTWTKADMSKLDFTDTIAAEDEKPMTLPSIFGLIGFALLASALAIRLGELLPEVGAVIDGTAWTILIVSVLGLAIGSTRFGRTAGSNELATILLYLIIGIIASGSDFTSLAEAPLYLVAGIIVLVVHIVIMLIYAKLTRTELFSIAVASTANIGGIASAPVVAGAFNRQLVPVGVLFALMGTFLGTFLGLWSAQILSGLA
>NZ_CP051626.1|WP_035321156.1|3517402_3517711_-|DUF3870-domain-containing-protein
MSDTIYLTGEAKAPSNNPITSQFGLFYVAFEIAPDTHRILDVDCTATLALTRNFIRSLFVDADITDPGRLIERIQRRYHGSSQKALITAVNNAAKKYREVAA
>NZ_CP051626.1|WP_169253255.1|3517825_3518626_-|serine-hydrolase
MSELRFDGLPGVRFSALAFDVDSGERVFAHNENDELDTASMGKVFLLHTALQMAVDGTLDLEERLHRRPSERVDESGIWYLMEQDDLSIFDVALLIGAFSDNFATNVLIRRVGLANVADQVVDLGYRNSGLHDFLRWPRPAKAPRTLSTGTAAELSDFMARHAKDEFWDESTNEIFRRWLGAGADTSMVASAFDLDPLAHYNYQRDVWVWNKTGTNGTIRADAGIVMTRTRRVAYAVFANWEPGTDRVVDVMPVMREAGDAIHRFL
>NZ_CP051626.1|WP_169253256.1|3518622_3519840_-|LD-carboxypeptidase
MSRQDSAGAVGAGGAAPAEDRVGRPAPSPYLRTAPLAAGDTVRLIAPSGPTDEESLQRAIAQLESWGLTVVPGGNVRGRHPRVTYLAGTDAERRCDLVDAWCDPDTDAVIALRGGFGAMRLLDGIDFDLMRRHMLRRDGRPKLLTGSSDITALHQAWEHHLGVATLFCPMVGNDPFKNSTVVPDEVASWLFQPWGGRELGFPADISAGAAADASADENRSPSDISDAEKSPKATTFLPDTAADDAARPLSRAQTLVPGEAKGRLGGGNLSLIAAGMGSPELSDVRERRERQGPSILMLEDVDEELYRLDNLMVQLVRGGWFTSADAVVLGSWQDCAAVHEVEALMIDYLGGLGVPIVSEMGFGHDPDAPSAPLGVDVTLEAEPGERPRLWVDAPANTTAEGETRS
>NZ_CP051626.1|WP_169253257.1|3519832_3521488_-|ABC-transporter-ATP-binding-protein
MTDLQFENVSITYRSSSDRGDVVAVQDVSLDLPSGATLGIAGESGSGKSTLIMSALRLLPKSARLDGRVLLGGQDIRELSFGQIRAVRWAQASIVFQGALHSLNPVREVGSQIIEALEHHSKDTWTTPQKRRDRMFELLAEVNLEAAKSSAYPHELSGGQKQRIMIAMALACEPDIIIADEPTTALDVIVQKQILTGLARLVAERGISLLMISHDLAVLSAVCADLAIMRHGRLVEYGPSDDVCLSPQEDYTQQLAGAFPQIGDPESRLNPRTRRPAEVARAEPFTMTDEVVLEAKDLSVSFDTRRGRERAVRGVDLQLKKAEILAVVGQSGSGKTTLARSLLELQEVEAGSQLFFAGKPLPRKAKELRAFRRQVQMILQDPAGSLNPKRSVYEAVVEGLKVQGIKDREYERVVGALAAAELTPAEDYLESIPQELSGGQRQRVVIAGALALDPQVLIADEPVASLDASVRGEILSLFLALKKNLGMSALIITHDLGLAWNIADTVAVMKRGEIVEYGEVEKVLSDPQHEYTQELLAAVPRLGSQSLVRNE
>NZ_CP051626.1|WP_169253258.1|3521487_3522399_-|ABC-transporter-permease
MSANTPAVDGAKLVRERRLNNAKKNWALFRSDAPALIGAVVLLFFIVIAIAAPLIAPASMLDVTKQLDVPRYAPPSLDHPLGTDDLGREMWVRILWGARVSILVGVAATVMSMLIGTIMGLAAGHFSGLFGGIIMRIVDFFIVLPSLLLAIVLSSVLERGVFTIVVAIGLTSWASTARIVRSQTLSVESRLYIERARILGAGHSHILFRHLLPAVMPLVLANTTLTVGGAIIAESTLSFLGLGDTSKESWGTILKNSMDVSAATSGYWWYVLTPGVAILLVVLAFTMVGRAFEAIINPALRSR
>NZ_CP051626.1|WP_169253978.1|3522398_3523391_-|ABC-transporter-permease
MDEPPAGGSFARYFLRKLGGAATSMVLVIVLGFFAFRMLPGDPVLKIAKERPMSPAQIAELRSQYGLDKPVIVQFWDYLVGIVTGDLGESYVYRKSVSSLIGDYLGPTLLLTGTAAVIAIALGLWLGQLSAWRRNSLFDKLASSTSLIFWSVPTFWLGLILLMIFGGTLQWLPTGGMITPGLDPWSPAGIIDVITHLILPVVSLVAVVYAQFLMIMRASLLEEMSEDYLTTARAKGLTEDEVRRRHAVPNALLPTVTVVFLHIGGLIAGAVTVEAVFSWPGLGKLTFEAIRGPDLPLLQGTFVVFSALIIVMNLAADIVYRFLDPRVRRV
>NZ_CP051626.1|WP_169253259.1|3523633_3525466_-|ABC-transporter-substrate-binding-protein
MVTQHSLRRTVRVSLRRCLAGIAALALAGSMAASPAQAADSEAPAAENVLRIATDGFIDSFNPFTSFYLVPTNTFRYMYENLVANDAKDGSVTEGLATEWNTDSDGKVWTYTIRPDMKWSDGEPLTSKDVAWTYNQMMDNDEMAVANGSLVENFAKVEAPDDSTVKITLKKAQANNPGQEIPVVPEHVWSKIDNPGEFKNDEKSVGSGPFQLDSYEANKSITLKANPNFWRGKPKLDEIQYRYYTNSDAQVQAIRSGEVDFITGLSPDQFTALENADNVELNDGNGRRFNGISINPGVADADGKEFGTGNEALGDKKVRQAIRAGIDTETLRKQVMQDYAQPATSFIPAVYPDWALSPDNPVVSGFDVDRAKTLLDDAGWKEGSDGIREKDGEKLQLRFLTDADVPTEQSTAKFLKPWMKDIGIDLKNESTDADTESERTTKGDYDMYFSGWSINPDPDYQLSINTCGQRPDAEGNGGTSQDGWCNKEFDKLYQAQHVELDQAKRQELVQKALAIHYEEAPSVTLWYPNQLEAYRSDRFENFTKQPSDGGAIANQVGYWGYSSVEPVSAGEATGGGMGAGGWIGIGAAVIVVLGGGGWLLSRRRKSDDRE
>NZ_CP051626.1|WP_169253260.1|3525752_3527825_-|TRAP-transporter-permease
MSEDSTPTRPSAATAGPGADEVAAGERASADVLAKHDTSSRYRKDLGWWVWVVGGLSIAFTVYHLYAALERPFNTWMHTSLHLAGATALIFFLYPPSRRLLDAPATGNRVADALIGRGSRIPWYDVLLGFAGLGCNLYVFVEYSRLVSNSVQILGYSNLDYFVAILGVLLILEATRRCVGLPIVIIGGIAILYGLFGNYSPVFTHSGMSLEDFATTMFLSNGSGIFGTPIQVSANFIFLFLFFAVMLVHTNIGQFFNDLAFRLTGRFTGGPAKAAVVASGLQGMVSGSSVANTVASGSFTIPLMKRSGFKPHFAAATEATASTGGQLMPPIMGAAAFIMAQNVPDLEYNGLIVIAIIPAILYFLGAFLSIHFEAKTDGILGLSKASLPDGKELLKRLDLLLPLAVIILTLLSGMSPIRAALFGIGTAFFLSFLRKSTRMDPRGFVTLLVEGARTALPVIAACATAGIVAGTVTATGLGGQLGKGLVDLAGGNFFIVLVMVMIACIVLGMGLPTTANYVVTATVAAPILYNNFDVPLIAAHMFVFFFGILADITPPVCLAAYAGAGIARANPMRAGVTAVRIAIAGFLIPYVFILEPALLLQGTWQELLLALVTVILGMIGVSSGLAGYFMGRANIVERVLLLAAGITLIYPNIWVSLVGLVVLVAVALIQRLRKATTTTEIAAQRAAATA
>NZ_CP051626.1|WP_169253261.1|3527821_3528805_-|TAXI-family-TRAP-transporter-solute-binding-subunit
MNIRRMTVAAVAAVALALTGCGSDGGSGGGGETTDDLTLGTGGTSGTYYPLGGELASIFEDNVDGVTVNYVESGASAENLGKIYQGEWQLGFTQSDTANTAVNGELEDLDGTKIDNVGWLASLYPEAAHIIVREDSGIESVEDLKGKKIAVGDAGSGTRAISDAILDAAGIGESDYTPEITDFGASTDMLADKQIDATIFVVGTPVAGLTQLAATTDVKLLGLDDDTTKTIEEGSGAESYDIPADAYDFLDEDVPTVSVFASLVASTDQVSEDTAYNLTKALFEHTDDITLDVGKLITKDSAMLGVGDVPLHPGAQKYFEEEGIELP

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

Click the colored protein region to show detailed information

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

DBSCAN-SWA_1

1879687 : 1946188

Streptococcus_phage(23.08%)

holin,transposase,tRNA,protease

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_169253834.1\|1879687_1880248_+\|protease	ATP-dependent Clp protease proteolytic subunit	A0A223W000	Agrobacterium_phage	2.4e-46	52.2
WP_169252137.1\|1880274_1880919_+\|protease	ATP-dependent Clp protease proteolytic subunit	A0A223W000	Agrobacterium_phage	3.1e-37	43.3
WP_169252138.1\|1881115_1882399_+\|protease	ATP-dependent Clp protease ATP-binding subunit ClpX	G3M9Z9	Bacillus_virus	2.0e-136	58.7
WP_169252139.1\|1882411_1883698_+	MFS transporter	NA	NA	NA	NA
WP_169252140.1\|1883978_1884731_-	AIM24 family protein	NA	NA	NA	NA
WP_169252141.1\|1884900_1887546_-\|tRNA	valine--tRNA ligase	A0A2K9KZB8	Tupanvirus	2.4e-160	37.4
WP_169252142.1\|1887734_1888925_+	acyltransferase family protein	A0A0F6TJ51	Escherichia_coli_O157_typing_phage	9.0e-06	27.9
WP_169252143.1\|1889004_1889760_+	SDR family oxidoreductase	NA	NA	NA	NA
WP_169252144.1\|1890074_1893338_+\|tRNA	isoleucine--tRNA ligase	A0A2K9L260	Tupanvirus	2.1e-153	32.7
WP_169252145.1\|1893334_1894831_+	bifunctional folylpolyglutamate synthase/dihydrofolate synthase	NA	NA	NA	NA
WP_025776799.1\|1894827_1895193_+	DUF4233 domain-containing protein	NA	NA	NA	NA
WP_169252146.1\|1895276_1895696_+	nucleoside-diphosphate kinase	D2E8E1	Anguillid_herpesvirus	6.1e-26	43.5
WP_169252147.1\|1895849_1896497_-	vitamin K epoxide reductase family protein	NA	NA	NA	NA
WP_169252148.1\|1896741_1899780_+	Rne/Rng family ribonuclease	NA	NA	NA	NA
WP_169253835.1\|1899866_1900679_-	SPFH domain-containing protein	NA	NA	NA	NA
WP_169252149.1\|1901320_1902850_+	alanine:cation symporter family protein	NA	NA	NA	NA
WP_167195869.1\|1902975_1903293_+	chorismate mutase	NA	NA	NA	NA
WP_025776790.1\|1903540_1903849_+	50S ribosomal protein L21	NA	NA	NA	NA
WP_025776788.1\|1903864_1904116_+	50S ribosomal protein L27	NA	NA	NA	NA
WP_169252150.1\|1904218_1905784_+	GTPase ObgE	NA	NA	NA	NA
WP_169252151.1\|1905780_1906947_+	glutamate 5-kinase	A0A1X9I5D0	Streptococcus_phage	7.1e-56	38.9
WP_101593614.1\|1906950_1908240_+	glutamate-5-semialdehyde dehydrogenase	A0A1X9I5D4	Streptococcus_phage	9.2e-89	46.2
WP_155807341.1\|1908413_1908575_+	hypothetical protein	NA	NA	NA	NA
WP_035319614.1\|1908576_1909182_+	nicotinate-nucleotide adenylyltransferase	NA	NA	NA	NA
WP_169252152.1\|1909174_1910668_+	hypothetical protein	NA	NA	NA	NA
WP_051504967.1\|1910706_1911099_+	ribosome silencing factor	NA	NA	NA	NA
WP_101553974.1\|1911095_1911692_+	histidine phosphatase family protein	NA	NA	NA	NA
WP_169253836.1\|1911748_1912849_-	glycosyltransferase family 4 protein	NA	NA	NA	NA
WP_169252153.1\|1913010_1916049_+	DUF4040 family protein	NA	NA	NA	NA
WP_169252154.1\|1916045_1916378_+	cation:proton antiporter subunit C	NA	NA	NA	NA
WP_169252155.1\|1916374_1917892_+	monovalent cation/H+ antiporter subunit D family protein	NA	NA	NA	NA
WP_169252156.1\|1917891_1918266_+	Na+/H+ antiporter subunit E	NA	NA	NA	NA
WP_169252157.1\|1918262_1918523_+	transporter	NA	NA	NA	NA
WP_169252158.1\|1918522_1918912_+	cation:proton antiporter	NA	NA	NA	NA
WP_169252159.1\|1918975_1919698_-	alpha-ketoglutarate-dependent dioxygenase AlkB	NA	NA	NA	NA
WP_169252160.1\|1919781_1920993_-	FAD-dependent oxidoreductase	NA	NA	NA	NA
WP_169252161.1\|1921344_1921701_+	hypothetical protein	NA	NA	NA	NA
WP_169253837.1\|1921854_1923165_+	family 1 glycosylhydrolase	A0A0B5JD41	Pandoravirus	1.0e-58	35.5
WP_169253838.1\|1923230_1924451_+	MFS transporter	NA	NA	NA	NA
WP_169252162.1\|1924482_1925025_-	DUF1905 domain-containing protein	NA	NA	NA	NA
WP_169253839.1\|1925243_1926692_-	3-hydroxyacyl-CoA dehydrogenase	NA	NA	NA	NA
WP_169252163.1\|1926715_1927627_-	3-keto-5-aminohexanoate cleavage protein	A0A1V0SL81	Klosneuvirus	1.0e-25	27.9
WP_169252164.1\|1927623_1928580_-	TetR family transcriptional regulator	NA	NA	NA	NA
WP_169252165.1\|1928740_1930114_+	aminotransferase class V-fold PLP-dependent enzyme	NA	NA	NA	NA
WP_169252166.1\|1930174_1930870_-	hypothetical protein	NA	NA	NA	NA
WP_169252167.1\|1930978_1932469_+	PLP-dependent aminotransferase family protein	NA	NA	NA	NA
WP_169252168.1\|1932512_1933292_+	YggS family pyridoxal phosphate-dependent enzyme	NA	NA	NA	NA
WP_101553988.1\|1933309_1934272_+	arsenic resistance protein	NA	NA	NA	NA
WP_169252169.1\|1934304_1935768_+	DNA-3-methyladenine glycosylase 2 family protein	NA	NA	NA	NA
WP_169252170.1\|1935769_1936348_+	methylated-DNA--[protein]-cysteine S-methyltransferase	M1PFU9	Streptococcus_phage	1.2e-19	50.0
WP_169252171.1\|1937290_1937860_-\|transposase	transposase	NA	NA	NA	NA
WP_101553991.1\|1938287_1938515_-	hypothetical protein	NA	NA	NA	NA
WP_101553992.1\|1939380_1940286_+	universal stress protein	NA	NA	NA	NA
WP_169253840.1\|1940386_1941163_+	alpha/beta hydrolase	NA	NA	NA	NA
WP_169252172.1\|1941255_1941486_-	hypothetical protein	NA	NA	NA	NA
WP_169252173.1\|1941558_1941978_-\|holin	phage holin family protein	NA	NA	NA	NA
WP_169252174.1\|1942230_1943541_+	MFS transporter	NA	NA	NA	NA
WP_169252175.1\|1943688_1945158_+	MFS transporter	A0A0P0IY73	Acinetobacter_phage	5.0e-75	36.5
WP_164742880.1\|1945378_1946188_-\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA

DBSCAN-SWA_2

2021331 : 2044818

Gordonia_phage(66.67%)

transposase,tRNA

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_169252224.1\|2021331_2022009_+\|tRNA	leucyl/phenylalanyl-tRNA--protein transferase	NA	NA	NA	NA
WP_169252225.1\|2022119_2022992_+	cytochrome c oxidase subunit II	NA	NA	NA	NA
WP_169252226.1\|2022988_2024683_+	cytochrome c oxidase subunit I	NA	NA	NA	NA
WP_169252227.1\|2024679_2025081_+	cytochrome c oxidase subunit 4	NA	NA	NA	NA
WP_169252228.1\|2026269_2026716_-	hypothetical protein	NA	NA	NA	NA
WP_169252229.1\|2026712_2027201_-	hypothetical protein	NA	NA	NA	NA
WP_169252230.1\|2028516_2029470_-	cytochrome c oxidase assembly protein	NA	NA	NA	NA
WP_169252231.1\|2034053_2034362_-\|transposase	transposase	NA	NA	NA	NA
WP_169253849.1\|2034448_2035327_+\|transposase	IS5 family transposase	NA	NA	NA	NA
WP_169253850.1\|2035385_2036510_+\|transposase	IS701 family transposase	NA	NA	NA	NA
WP_169252232.1\|2036845_2037457_-	DUF5134 domain-containing protein	NA	NA	NA	NA
WP_169252233.1\|2037637_2037988_+	transcriptional regulator	NA	NA	NA	NA
WP_169252234.1\|2037999_2038776_+	M56 family metallopeptidase	NA	NA	NA	NA
WP_169252235.1\|2038826_2040896_+	cytochrome c oxidase assembly protein	NA	NA	NA	NA
WP_169252236.1\|2040885_2043195_+	heavy metal translocating P-type ATPase	A0A218MNH6	uncultured_virus	3.8e-85	32.3
WP_169252237.1\|2043387_2043627_-\|transposase	transposase	NA	NA	NA	NA
WP_169252238.1\|2043762_2044425_-\|transposase	IS3 family transposase	A0A1B3AZE5	Gordonia_phage	3.0e-35	47.4
WP_169252239.1\|2044512_2044818_-\|transposase	transposase	A0A1B3AZF8	Gordonia_phage	3.5e-15	45.0

DBSCAN-SWA_3

3366395 : 3437809

Bacillus_phage(27.27%)

holin,transposase,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_169253151.1\|3366395_3368477_-\|holin	choline BCCT transporter BetT	A0A2I7QNT1	Vibrio_phage	2.3e-09	22.1
WP_169253152.1\|3368709_3370089_-	short-chain fatty acid transporter	NA	NA	NA	NA
WP_169253153.1\|3370242_3371622_-	NAD-dependent succinate-semialdehyde dehydrogenase	NA	NA	NA	NA
WP_169253154.1\|3371843_3373103_-	hypothetical protein	NA	NA	NA	NA
WP_169253155.1\|3373276_3373630_+	SnoaL-like domain-containing protein	NA	NA	NA	NA
WP_169253156.1\|3373644_3374445_-	DUF981 family protein	NA	NA	NA	NA
WP_169253157.1\|3374622_3375543_-	hydroxylacyl-CoA dehydrogenase	NA	NA	NA	NA
WP_169253158.1\|3375707_3376571_+	hypothetical protein	NA	NA	NA	NA
WP_169253159.1\|3376616_3377855_+	chromate efflux transporter	NA	NA	NA	NA
WP_169253160.1\|3377922_3379554_-	long-chain-fatty-acid--CoA ligase	NA	NA	NA	NA
WP_169253161.1\|3379817_3380579_-	enoyl-CoA hydratase	NA	NA	NA	NA
WP_169253162.1\|3380759_3381743_-	cytochrome c oxidase assembly protein	NA	NA	NA	NA
WP_169253163.1\|3381948_3382521_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_169253164.1\|3382520_3383780_-	PLP-dependent transferase	NA	NA	NA	NA
WP_169253165.1\|3383832_3384750_-	LysR family transcriptional regulator	NA	NA	NA	NA
WP_169253166.1\|3384836_3385979_+	putative sulfate exporter family transporter	NA	NA	NA	NA
WP_169251415.1\|3386296_3387364_+\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_169252171.1\|3388314_3388884_-\|transposase	transposase	NA	NA	NA	NA
WP_169253167.1\|3389145_3390531_+	C4-dicarboxylate ABC transporter	NA	NA	NA	NA
WP_169253168.1\|3390622_3391210_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_169253169.1\|3391390_3391717_+	N-acetyltransferase	NA	NA	NA	NA
WP_169253170.1\|3392084_3393542_+	NAD-dependent succinate-semialdehyde dehydrogenase	NA	NA	NA	NA
WP_169253171.1\|3393613_3394651_-	alcohol dehydrogenase catalytic domain-containing protein	NA	NA	NA	NA
WP_169253172.1\|3394680_3396045_-	shikimate transporter	NA	NA	NA	NA
WP_169253173.1\|3396298_3396808_+	hypothetical protein	NA	NA	NA	NA
WP_169253832.1\|3397189_3398359_+\|transposase	IS30 family transposase	Q9MBM9	Staphylococcus_prophage	2.3e-38	34.2
WP_169253174.1\|3398462_3400631_-	hypothetical protein	NA	NA	NA	NA
WP_169253175.1\|3400749_3401346_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_169253176.1\|3401454_3402357_-	UTP--glucose-1-phosphate uridylyltransferase GalU	A0A127AW70	Bacillus_phage	1.3e-68	46.7
WP_169253968.1\|3402348_3403167_+	hypothetical protein	NA	NA	NA	NA
WP_169253177.1\|3403290_3403614_+	FmdB family transcriptional regulator	NA	NA	NA	NA
WP_169253178.1\|3403724_3404354_+	hypothetical protein	NA	NA	NA	NA
WP_169253179.1\|3404594_3405056_+	large conductance mechanosensitive channel protein MscL	NA	NA	NA	NA
WP_169253180.1\|3405190_3405469_-	hypothetical protein	NA	NA	NA	NA
WP_169253181.1\|3405461_3410498_-	DUF4011 domain-containing protein	NA	NA	NA	NA
WP_169253182.1\|3410855_3411920_-	universal stress protein	NA	NA	NA	NA
WP_169253183.1\|3412065_3412566_-	HNH endonuclease	H6WG01	Cyanophage	6.4e-22	41.4
WP_169253184.1\|3412851_3413010_-	hypothetical protein	NA	NA	NA	NA
WP_169253185.1\|3413161_3413989_-	C40 family peptidase	D2KRB9	Lactobacillus_phage	3.1e-05	32.2
WP_169253186.1\|3414445_3415132_-	metal-dependent transcriptional regulator	NA	NA	NA	NA
WP_169253187.1\|3415396_3416869_-	aldehyde dehydrogenase family protein	NA	NA	NA	NA
WP_169253188.1\|3416945_3417617_-	pyridoxamine 5'-phosphate oxidase	NA	NA	NA	NA
WP_169253189.1\|3417792_3418974_+	phosphoserine transaminase	NA	NA	NA	NA
WP_169253190.1\|3419343_3419841_-	DUF456 domain-containing protein	NA	NA	NA	NA
WP_169253191.1\|3420017_3421295_-	MFS transporter	D0R099	Streptococcus_phage	7.9e-08	21.7
WP_169253192.1\|3421303_3422263_-	DUF3027 domain-containing protein	NA	NA	NA	NA
WP_101594737.1\|3422262_3422643_-	cold shock domain-containing protein	Q9AZD3	Lactococcus_phage	1.3e-06	41.0
WP_025780328.1\|3423077_3423308_-	hypothetical protein	NA	NA	NA	NA
WP_169253193.1\|3423382_3425533_+	hypothetical protein	NA	NA	NA	NA
WP_169253194.1\|3425669_3427304_+	DEAD/DEAH box helicase	B2CRJ8	Acidianus_filamentous_virus	1.2e-11	23.6
WP_169253195.1\|3427378_3428344_-	EamA family transporter	NA	NA	NA	NA
WP_169253196.1\|3428666_3429266_+	CGNR zinc finger domain-containing protein	NA	NA	NA	NA
WP_169253197.1\|3429301_3429991_+	hypothetical protein	NA	NA	NA	NA
WP_169253198.1\|3430260_3431019_+	response regulator transcription factor	W8CYM9	Bacillus_phage	4.2e-33	35.0
WP_169253969.1\|3431124_3432993_+	HAMP domain-containing histidine kinase	W8CYF6	Bacillus_phage	4.2e-10	46.6
WP_169253199.1\|3432989_3435017_+\|protease	trypsin-like serine protease	A0A1B1IT49	uncultured_Mediterranean_phage	1.1e-11	25.3
WP_035321190.1\|3435275_3435563_+	WXG100 family type VII secretion target	NA	NA	NA	NA
WP_025780460.1\|3435787_3436537_+	PspA/IM30 family protein	NA	NA	NA	NA
WP_025780459.1\|3436533_3436818_+	hypothetical protein	NA	NA	NA	NA
WP_169253200.1\|3436897_3437809_+\|protease	zinc metalloprotease HtpX	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_CP051626

Click the left colored region to show detailed information

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

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection