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_CP054128	Pseudomonas fluorescens strain MPDS chromosome, complete genome	3 crisprs	DEDDh,csa3,cas3,WYL,PD-DExK,DinG,RT	0	0	6	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP054128_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP054128_1

1429887-1429985

Orphan

Consensus_repeat	Method
CGCGAGGCGGCCTGACAGCCGGCCT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP054128_1

>merge|NZ_CP054128|1|1429887-1429985|CRISPRCasFinder
CGCGAGGCGGCCTGACAGCCGGCCTGGTTCTTTCGGTCGTACACCTGTCAGATCTGTGGGAGCAAAGCTTGCTCGCGAAGGCGGCCTGACAGCCGGCCT

>NZ_CP054128|1|1|1429887-1429985|CRISPRCasFinder
CGCGAGGCGGCCTGACAGCCGGCCT	GGTTCTTTCGGTCGTACACCTGTCAGATCTGTGGGAGCAAAGCTTGCTC
GCGAAGGCGGCCTGACAGCCGGCCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP054128.1\|WP_047228828.1\|1438525_1438780_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP054128.1\|WP_107321911.1\|1421545_1422616_+\|undecaprenyldiphospho-muramoylpentapeptide-beta-N-acetylglucosaminyltransferase	unknown	unknown	gnl\|CDD\|234825
NZ_CP054128.1\|WP_047228825.1\|1433343_1434015_-\|heavy-metal-response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|130454
NZ_CP054128.1\|WP_076383614.1\|1425915_1427175_+\|cell-division-protein-FtsA	unknown	unknown	gnl\|CDD\|273483
NZ_CP054128.1\|WP_047228829.1\|1438807_1439776_-\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|176114
NZ_CP054128.1\|WP_047228830.1\|1440087_1441560_+\|efflux-transporter-outer-membrane-subunit	unknown	unknown	gnl\|CDD\|273830
NZ_CP054128.1\|WP_173406581.1\|1437131_1438289_-\|efflux-RND-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|183194
NZ_CP054128.1\|WP_047228816.1\|1417907_1418990_+\|phospho-N-acetylmuramoyl-pentapeptide--transferase	unknown	unknown	gnl\|CDD\|234638
NZ_CP054128.1\|WP_047228822.1\|1425033_1425900_+\|cell-division-protein-FtsQ/DivIB	unknown	unknown	gnl\|CDD\|224505
NZ_CP054128.1\|WP_160893488.1\|1420344_1421556_+\|putative-lipid-II-flippase-FtsW	unknown	unknown	gnl\|CDD\|274232
NZ_CP054128.1\|WP_024617598.1\|1443749_1443950_+\|DUF1656-domain-containing-protein	unknown	unknown	gnl\|CDD\|377931
NZ_CP054128.1\|WP_173406582.1\|1441567_1443760_+\|FUSC-family-protein	unknown	unknown	gnl\|CDD\|377393
NZ_CP054128.1\|WP_173406580.1\|1434024_1437135_-\|multidrug-efflux-RND-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|182501
NZ_CP054128.1\|WP_047228820.1\|1422608_1424069_+\|UDP-N-acetylmuramate--L-alanine-ligase	unknown	unknown	gnl\|CDD\|234757
NZ_CP054128.1\|WP_171061319.1\|1431979_1433347_-\|heavy-metal-sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|273593
NZ_CP054128.1\|WP_173407514.1\|1430237_1431734_-\|GGDEF-domain-containing-protein	unknown	unknown	gnl\|CDD\|143635
NZ_CP054128.1\|WP_076383613.1\|1424065_1425031_+\|D-alanine--D-alanine-ligase	unknown	unknown	gnl\|CDD\|234948
NZ_CP054128.1\|WP_107321910.1\|1418995_1420342_+\|UDP-N-acetylmuramoyl-L-alanine--D-glutamate-ligase	unknown	unknown	gnl\|CDD\|235160
NZ_CP054128.1\|WP_047228824.1\|1427275_1428469_+\|cell-division-protein-FtsZ	unknown	unknown	gnl\|CDD\|236468
NZ_CP054128.1\|WP_030139673.1\|1428581_1429493_+\|UDP-3-O-acyl-N-acetylglucosamine-deacetylase	unknown	unknown	gnl\|CDD\|237294

Protein	Function_ID	Function_description	E-value
NZ_CP054128.1\|WP_107321911.1\|1421545_1422616_+\|undecaprenyldiphospho-muramoylpentapeptide-beta-N-acetylglucosaminyltransferase	gnl\|CDD\|234825	PRK00726, murG, undecaprenyldiphospho-muramoylpentapeptide beta-N- acetylglucosaminyltransferase; Provisional.	3.03924e-167
NZ_CP054128.1\|WP_047228825.1\|1433343_1434015_-\|heavy-metal-response-regulator-transcription-factor	gnl\|CDD\|130454	TIGR01387, Transcriptional_regulatory_protein_PcoR, heavy metal response regulator. Members of this family contain a response regulator receiver domain (pfam00072) and an associated transcriptional regulatory region (pfam00486). This group is separated phylogenetically from related proteins with similar architecture and contains a number of proteins associated with heavy metal resistance efflux systems for copper, silver, cadmium, and/or zinc. Most members encoded by genes adjacent to genes for encoding a member of the heavy metal sensor histidine kinase family (TIGRFAMs:TIGR01386), its partner in the two-component response regulator system. [Regulatory functions, DNA interactions].	9.65913e-100
NZ_CP054128.1\|WP_076383614.1\|1425915_1427175_+\|cell-division-protein-FtsA	gnl\|CDD\|273483	TIGR01174, Cell_division_protein_FtsA, cell division protein FtsA. This bacterial cell division protein interacts with FtsZ, the bacterial homolog of tubulin. It is an ATP-binding protein and shows structural similarities to actin and heat shock cognate protein 70. [Cellular processes, Cell division].	0
NZ_CP054128.1\|WP_047228829.1\|1438807_1439776_-\|LysR-family-transcriptional-regulator	gnl\|CDD\|176114	cd08422, PBP2_CrgA_like, The C-terminal substrate binding domain of LysR-type transcriptional regulator CrgA and its related homologs, contains the type 2 periplasmic binding domain. This CD includes the substrate binding domain of LysR-type transcriptional regulator (LTTR) CrgA and its related homologs. The LTTRs are acting as both auto-repressors and activators of target promoters, controlling operons involved in a wide variety of cellular processes such as amino acid biosynthesis, CO2 fixation, antibiotic resistance, degradation of aromatic compounds, nodule formation of nitrogen-fixing bacteria, and synthesis of virulence factors, to name a few. In contrast to the tetrameric form of other LTTRs, CrgA from Neisseria meningitides assembles into an octameric ring, which can bind up to four 63-bp DNA oligonucleotides. Phylogenetic cluster analysis further showed that the CrgA-like regulators form a subclass of the LTTRs that function as octamers. The CrgA is an auto-repressor of its own gene and activates the expression of the mdaB gene which coding for an NADPH-quinone reductase and that its action is increased by MBL (alpha-methylene-gamma-butyrolactone), an inducer of NADPH-quinone oxidoreductase. The structural topology of this substrate-binding domain 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.	8.57268e-65
NZ_CP054128.1\|WP_047228830.1\|1440087_1441560_+\|efflux-transporter-outer-membrane-subunit	gnl\|CDD\|273830	TIGR01845, Outer_membrane_protein_OprM, efflux transporter, outer membrane factor (OMF) lipoprotein, NodT family. Members of this model comprise a subfamily of the Outer Membrane Factor (TCDB 1.B.17) porins. OMF proteins operate in conjunction with a primary transporter of the RND, MFS, ABC, or PET systems, and a MFP (membrane fusion protein) to tranport substrates across membranes. The complex thus formed allows transport (export) of various solutes (heavy metal cations; drugs, oligosaccharides, proteins, etc.) across the two envelopes of the Gram-negative bacterial cell envelope in a single energy-coupled step. Current data suggest that the OMF (and not the MFP) is largely responsible for the formation of both the trans-outer membrane and trans-periplasmic channels. The roles played by the MFP have yet to be determined. [Cellular processes, Detoxification, Transport and binding proteins, Porins].	3.00341e-96
NZ_CP054128.1\|WP_173406581.1\|1437131_1438289_-\|efflux-RND-transporter-periplasmic-adaptor-subunit	gnl\|CDD\|183194	PRK11556, PRK11556, MdtA/MuxA family multidrug efflux RND transporter periplasmic adaptor subunit.	4.34124e-79
NZ_CP054128.1\|WP_047228816.1\|1417907_1418990_+\|phospho-N-acetylmuramoyl-pentapeptide--transferase	gnl\|CDD\|234638	PRK00108, mraY, phospho-N-acetylmuramoyl-pentapeptide-transferase; Provisional.	0
NZ_CP054128.1\|WP_047228822.1\|1425033_1425900_+\|cell-division-protein-FtsQ/DivIB	gnl\|CDD\|224505	COG1589, FtsQ, Cell division septal protein [Cell envelope biogenesis, outer membrane].	5.45829e-54
NZ_CP054128.1\|WP_160893488.1\|1420344_1421556_+\|putative-lipid-II-flippase-FtsW	gnl\|CDD\|274232	TIGR02614, Putative_lipid_II_flippase_FtsW, cell division protein FtsW. This family consists of FtsW, an integral membrane protein with ten transmembrane segments. In general, it is one of two paralogs involved in peptidoglycan biosynthesis, the other being RodA, and is essential for cell division. All members of the seed alignment for this model are encoded in operons for the biosynthesis of UDP-N-acetylmuramoyl-pentapeptide, a precursor of murein (peptidoglycan). The FtsW designation is not used in endospore-forming bacterial (e.g. Bacillus subtilis), where the member of this family is designated SpoVE and three or more RodA/FtsW/SpoVE family paralogs are present. SpoVE acts in spore cortex formation and is dispensible for growth. Biological rolls for FtsW in cell division include recruitment of penicillin-binding protein 3 to the division site. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan, Cellular processes, Cell division].	1.33907e-146
NZ_CP054128.1\|WP_024617598.1\|1443749_1443950_+\|DUF1656-domain-containing-protein	gnl\|CDD\|377931	pfam07869, DUF1656, Protein of unknown function (DUF1656). This family contains bacterial proteins, many of which are hypothetical. Some proteins in this family are putative membrane proteins.	9.35958e-12
NZ_CP054128.1\|WP_173406582.1\|1441567_1443760_+\|FUSC-family-protein	gnl\|CDD\|377393	pfam04632, FUSC, Fusaric acid resistance protein family. This family includes a conserved region found in two proteins associated with fusaric acid resistance, FusC from Burkholderia cepacia and fdt-2 from Klebsiella oxytoca. These proteins are likely to be membrane transporter proteins.	0
NZ_CP054128.1\|WP_173406580.1\|1434024_1437135_-\|multidrug-efflux-RND-transporter-permease-subunit	gnl\|CDD\|182501	PRK10503, PRK10503, MdtB/MuxB family multidrug efflux RND transporter permease subunit.	0
NZ_CP054128.1\|WP_047228820.1\|1422608_1424069_+\|UDP-N-acetylmuramate--L-alanine-ligase	gnl\|CDD\|234757	PRK00421, murC, UDP-N-acetylmuramate--L-alanine ligase; Provisional.	0
NZ_CP054128.1\|WP_171061319.1\|1431979_1433347_-\|heavy-metal-sensor-histidine-kinase	gnl\|CDD\|273593	TIGR01386, Probable_sensor_protein_PcoS, heavy metal sensor kinase. Members of this family contain a sensor histidine kinase domain (pfam00512) and a domain found in bacterial signal proteins (pfam00672). This group is separated phylogenetically from related proteins with similar architecture and contains a number of proteins associated with heavy metal resistance efflux systems for copper, silver, cadmium, and/or zinc.	2.25717e-136
NZ_CP054128.1\|WP_173407514.1\|1430237_1431734_-\|GGDEF-domain-containing-protein	gnl\|CDD\|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	1.02595e-63
NZ_CP054128.1\|WP_076383613.1\|1424065_1425031_+\|D-alanine--D-alanine-ligase	gnl\|CDD\|234948	PRK01372, ddl, D-alanine--D-alanine ligase; Reviewed.	0
NZ_CP054128.1\|WP_107321910.1\|1418995_1420342_+\|UDP-N-acetylmuramoyl-L-alanine--D-glutamate-ligase	gnl\|CDD\|235160	PRK03803, murD, UDP-N-acetylmuramoyl-L-alanyl-D-glutamate synthetase; Provisional.	0
NZ_CP054128.1\|WP_047228824.1\|1427275_1428469_+\|cell-division-protein-FtsZ	gnl\|CDD\|236468	PRK09330, PRK09330, cell division protein FtsZ; Validated.	0
NZ_CP054128.1\|WP_030139673.1\|1428581_1429493_+\|UDP-3-O-acyl-N-acetylglucosamine-deacetylase	gnl\|CDD\|237294	PRK13186, lpxC, UDP-3-O-acyl-N-acetylglucosamine deacetylase.	0

>NZ_CP054128.1|WP_030139673.1|1428581_1429493_+|UDP-3-O-acyl-N-acetylglucosamine-deacetylase
MIKQRTLKNIIRATGVGLHSGEKVYLTLKPAPVDTGIVFCRADLDPVVQIPARAENVGETTMSTTLVNGDTKVDTVEHLLSAMAGLGIDNAYVELSASEVPIMDGSAGPFVFLIQSAGLEEQDAAKKFIRILREVTVEDGDKRATFVPFEGFKVSFEIDFDHPVFRDRTQSASVDFSSTSFVKEVSRARTFGFMSDIEYLRKHNLALGGSVENAIVVDSDGVLNEDGLRYEDEFVKHKILDAIGDLYLLGNSLIGEFKGFKSGHALNNQLLRKLIEQKDAWEVVTFEDASTAPISYMRPVAAV
>NZ_CP054128.1|WP_047228824.1|1427275_1428469_+|cell-division-protein-FtsZ
MFELVDNIPASPVIKVIGVGGGGGNAVNHMVKSNIEGVEFICANTDAQALKNIGARTILQLGTGVTKGLGAGANPEVGRQAALEDRERIAEVLAGTNMVFITTGMGGGTGTGAAPIIAEVAKEMGILTVAVVTRPFPFEGRKRMQIADEGIRALSESVDSLITIPNEKLLTILGKDASLLSAFAKADDVLAGAVRGISDIIKRPGMINVDFADVRTVMSEMGMAMMGTGCASGPNRAREATEAAIRNPLLEDVNLQGARGILVNITAGPDLSLGEYSDVGSIIEAFASDHAMVKVGTVIDPDMRDELHVTVVATGLGAKIEKPMKVIDNTVQTSLASQPQQQAAARQEQPAVNYRDLDRPTVMRNQAQAGAATAAKMNPQDDLDYLDIPAFLRRQAD
>NZ_CP054128.1|WP_076383614.1|1425915_1427175_+|cell-division-protein-FtsA
MANVQSGKMIVGLDIGTSKVVALVGEVADDGTLVIVGIGTHPSRGLKKGVVVNIESTVQSIQRAIEEAQLMAGCRIHSAFVGVAGNHIRSLNSHGIVAIRDREVSSADLERVLDAAQAVAIPADQRVLHTLPQDYVIDNQEGVREPLGMSGVRLEAKVHVVTCAVNAAQNIEKCVRRCGLEIDDIILEQLASAYSVLTDDEKELGVCLVDIGGGTTDIAIFTEGAIRHTAVIPIAGDQVTNDIAMALRTPTQYAEEIKIRYACALAKLAGAGETIKVPSVGERPPRELSRQALAEVVEPRYDELFTLIQAELRRSGYEDLIPAGIVLTGGTSKMEGAVELAEEIFHMPVRLGVPHGVKGLDDVVRNPIYSTGVGLLMYGLQKQSDGVSFSGIGSRDSYNSDEPKAPLFERLQAWVKGNF
>NZ_CP054128.1|WP_047228822.1|1425033_1425900_+|cell-division-protein-FtsQ/DivIB
MQGASLRHQPSAPGRKPVPRGASRMVAKEPMSARLPKANFGFLKSLFWPVLLVALGFGTYEGAQRLLPYADRPIARINVQGDLSYISQQAVQQRIAPFVASSFFTIDLAGMRKELEQMPWIAHAEVRRVWPDQVSIRLEEQLPVARWGDESLLNNQGQAFTPRELANYEHLPQLFGPQRAQQKVMQQYQVLSQMLRPLGFSIARLELRERGSWFLTTGAGSSGPGIELLLGRGNQVEKMRRFIAIYDKTLKDQITNIARIDLRYANGLAVGWREPVAPTTAEPAVAKN
>NZ_CP054128.1|WP_076383613.1|1424065_1425031_+|D-alanine--D-alanine-ligase
MTAAYANLVSTLDPKAFGRVAVLFGGKSAEREVSLKSGNAVLQALQSAGVDAFGIDVGDDFLQRLLNEKIDRAFIILHGRGGEDGSMQGLLECLGIPYTGSGILASALAMDKLRTKQVWHSLGIPTPRHAVLASEADCISAATELGFPLIVKPAHEGSSIGMAKVTSLPELTAAWKDASSYDSQVLVEQWITGPEFTIATLRDQVLPPIALGTPHTFYDYDAKYVANDTQYRIPCGLDSAKEKQLMDLTAKACEALGIAGWGRADVMQDADGQFWFLEVNTAPGMTDHSLVPMAARAAGLDFQQLVLSILAASVGSQEPRG
>NZ_CP054128.1|WP_047228820.1|1422608_1424069_+|UDP-N-acetylmuramate--L-alanine-ligase
MVENRKAMPQPEMRRIRRIHFVGIGGVGMCGIAEVLLNLGYEVSGSDLKASPVTERLESFGAQIFIGHRAENAANADVLVVSSAVNTSNPEVATALERRIPVVPRAEMLAELMRYRHGIAVAGTHGKTTTTSLIASVFAAGGLDPTFVIGGRLNAAGTNAQLGTSRYLIAEADESDASFLHLQPLVAVVTNIDADHMATYDGDFNKLKKTFVEFLHNLPFYGLAVVCLDDPVVREILPLIKRPTVTYGFGEEVDVRAINVRQQGMQTFFTVLRPDREPLDVSVNMPGNHNVLNALATICIATDEGVSDEAIVQGLSGFQGVGRRFQVYGELPVDGGNVMLVDDYGHHPTEVAAVIKAVRGGWPERRLVMVYQPHRYSRTRDLYDDFVQVLADANVLLLMEVYPAGEEPIPGADSRQLCHSIRQRGQLDPIYIERGVDLAPLVKPLLRAGDILLCQGAGDIGGLAPKLLKSPLFAGAIVASSEGKLK
>NZ_CP054128.1|WP_107321911.1|1421545_1422616_+|undecaprenyldiphospho-muramoylpentapeptide-beta-N-acetylglucosaminyltransferase
MGANVLIMAGGTGGHVFPALACAREFQARGYTVHWLGTPRGIENELVPAAGLELHRISASGLRGKGKLSLLKAPLMLLKSIWQARAIIRRLRPVCVVGFGGYVTGPGGVAAKLAGVPVIVHEQNAVAGTANRLLVPLAARVCEAFPDTFTLSGSRRTTGNPVRTELFLDTPRPALAGRKARLLILGGSLGAEPLNKLLPEALSQVAPELRPEVFHQAGKNHDEVTAERYRAAGVEAQVQPFIKDMAQAYGWADLVVCRAGALTISELAAAGLPSMLVPLPHAIDDHQTRNADYLAREGAAFLMPQRTTGAADLAARLTEVLMQPQTIEDMARAARRLAKPDATVQVVDTCLEVAHG
>NZ_CP054128.1|WP_160893488.1|1420344_1421556_+|putative-lipid-II-flippase-FtsW
MMNIIKPYPSPLITGRGIDLDFPMLVGCLALLGLGLVMITSASSEVAAVQSGNTLYHMIRHLIYLVIGLVACIVTMMVPIATWQRLGWMMLLGAFGLLVMVLLPGIGREVNGSMRWIGFSFFNVQPSEIAKVFVVIYLAGYLVRRQKEVRESWMGFFKPFIVLLPMAGLLLMEPDFGATVVMMGAAAAMLFLGGVGLFRFTLMVALAVGAVTVLVQAQPYRMARLITFTDPWADQFGSGYQLTQALIAFGRGEWLGVGLGNSVQKQFYLPEAHTDFVFSVLAEELGVVGSLLTVGLFVFVCVRGMYIGLWAERAKQYFAAYVAYGLSFLWIGQFLINIGVNVGLLPTKGLTLPFLSYGGSSLVICCACLGLLLRIEWESRTHLGSEEMEFQESDFAEEPTHGR
>NZ_CP054128.1|WP_107321910.1|1418995_1420342_+|UDP-N-acetylmuramoyl-L-alanine--D-glutamate-ligase
MSLIASDHFRIVVGLGKSGMSLVRFLANRGVSFAVADTRENPPELATLRRDYPQVDVRCGELDVEFLCRADELYVSPGLALATPALQAAAARGVKLSGDIELFARHAKAPIIAISGSNAKSTVTTLVGEMAAAAGKRVAVGGNLGTPALDLLSDDVELYVMELSSFQLETTDHLGAEVATVLNISEDHMDRYSGLPAYHLAKHRIFRGARQVVFNRQDALTRPLLGEGMPCWSFGLGVPDFKGFGLREENGEKYLAFEFQNLMPVRELKIRGAHNQANALAALALGHAVGLPFDAMLSALRTFAGLEHRCQWVRDLDGVAWYNDSKATNVGAALAAIEGLGADIQGKLVLIAGGDGKGADFKDLRDPVAVNCRAVVLMGRDRELIAQALGDGVPLVRVASLDEAVQQCRALAQSGDAVLLSPACASFDMFKNYEERGQLFARAVEGLA
>NZ_CP054128.1|WP_047228816.1|1417907_1418990_+|phospho-N-acetylmuramoyl-pentapeptide--transferase
MLLLLAEYLQQFHKGFAVFQYLTLRGILGVLTALSLSLFLGPWMIRTLQNLQIGQSVRNDGPQSHLSKSGTPTMGGALILSSIGISTVLWADLANRYVWVVLLVTLLFGAIGWVDDYRKVIEKNSRGLPSRWKYFWQSVFGLGAAIFLYMTAASPVETTLILPMLKDYSIPLGAGFIVLTYLVIVGSSNAVNLTDGLDGLAIMPTVMVGGALGIFCYLSGNVKFAEYLLIPYVPGAGELIVFCGALIGAGLGFLWFNTYPAQVFMGDVGALALGAALGTIAVIVRQEIVLFIMGGVFVMETLSVVIQVASFKLTGRRVFRMAPIHHHFELKGWPEPRVIVRFWIITVILVLVGLATLKLR
>NZ_CP054128.1|WP_173407514.1|1430237_1431734_-|GGDEF-domain-containing-protein
MSASSATPGNTPFSIRSERVLVLASSLVVIAILSIVTFLLIREYAAAQQAATRSATNIVQLIDADVLRNVELYDLSLQGLVAAAQRNDLKDVSPTIRHLALFDRATAAPYKGDILLLDKRGNVVADSASIEPRKGNYADREYFQSHVHNPSPGMMISRPFRSRSAAQDWRISFSYRLNDEQGEFLGVAEAAMRLNYFNQLFKSLNIGHGGTVNLVSSEGFLLAQEPPLAEDLIGKDFSNRPNFMRILREGNGSFTSVSGQDQKPRLYTFSQVGDLPLIVVVALSSDEVFASWKRTALLVSGATGALCIGLLWLTWLLRHELRRRHHAERELAQLASIDSLTGLANRRTLDETLQQEWLRAQRSGQPLSVMMIDADHFKAFNDRHGHPSGDEALRTLAHLIGRHVRRPADLAARYGGEEFAVVLPETTTAGAFTMAQNIREAVEQLPPFITGAAPMTVSIGIATWAQGPYGELEQLMFAADKALYQAKASGRNRVVCAM
>NZ_CP054128.1|WP_171061319.1|1431979_1433347_-|heavy-metal-sensor-histidine-kinase
MTLPDSIALRLSGMFTLVAALVFLLIGGALYQQVEKGLGLLPEAELDARYSVLESTVGRYGTPEHWVKINNKLRLLGEEDKRIHFWIVSGDPRFEYGNPDPQIRAFAEGSLGKRDLKLAAQQYPMKVLVSQFPAKDQRPPLRFMIGIDTQTFYQTQHYLLVALVSLAIVGVILASLLGYWVARIGLKPLIKLSDEARRLTPPRLSGRLQMSPLAPELSQFVSSFNATLDRVEQAYSRLESFNADVAHELRSPLTNLIGQTQVALTRGRSAEHYFEVLQSNLEELERLRSIINDMLFLASADQGNKATKLTSTSLAGEVATTLDYLDFILEDAQVQVRVSGDAQANIEIAHLRRALINLLSNAVRHTAPGQVINVRIEALGDQITLAVTNPGEPIADEHLPRLFERFYRVDASRSNSGANHGLGLAIVKAIALMHGGDVFVRSDRGVNTFGIRLPA
>NZ_CP054128.1|WP_047228825.1|1433343_1434015_-|heavy-metal-response-regulator-transcription-factor
MRVLIIEDEEKTADYLHRGLSEQGYTVDVAPDGVEGLHLALESDYAVIVLDVMLPGLDGFGVLRALRARKQTPVIMLTARERVEDRIKGLRDGADDYLGKPFSFLELVARLQALTRRSGSHEPVQVSIADLWIDLISRKATRAGQRLDLTAKEFSLLSVLARRQGEILSKTAIAEMVWDINFDSDANVVEVAIKRLRAKLDGPFEQKLLHTIRGMGYVLESRE
>NZ_CP054128.1|WP_173406580.1|1434024_1437135_-|multidrug-efflux-RND-transporter-permease-subunit
MKGRGSVSAWCIDHPIATVLMTFALILLGLIAFPRLPVAPLPEAEFPTIQVRALLPGASPETMASSVATPLEVQFSAISGITQMTSSSALGSTNLTLQFSLDKSIDTAAQEVQAAINTASGKLPQDMPNLPTWRKVNPADSPVLILSISSSLMPGTELSDYVETLLARQLSQIDGVGQIYITGQQRPAIRVQASADRLAAIGLTLADIRVALQQASLNLAKGALYGESSVSTLSTNDQLFQPEEYGELIVSYKDGAPVHLKDVAKVINGSEDAYIQAWSDEQPGLNLVIFRQPGANIVDTVDRIQAALPTLEAMLPAAVQVKVLNDRTQTIRASLHEVEITLLIAVLLVVAVMALFLRQLSATLIVSAVLGVSLIASFALMYVMGFSLNNLTLVAIVISVGFVVDDAIVVVENIHRHLEAGDGMREAAIKGAGEIGFTVISISFSLIAAFIPLLFMGGVVGRLFKEFALTATSTILISVVVSLTLAPTLAALFMRAPTPHAHGKRSFGERLLGGYERTLRWALAHQRLMIGVFGVTLALAVAGYVFIPKGFFPVQDTGLVLGTSEAAADVSFPDMVAKHKALAEIVAADPAVQSFSHAVGVSGSNQTIANGRFWIALKPQDQRDVSASAFIDRIRPKLLGIPGVVLYLRAGQDINLSPGPSRAQYQYVLKSNDGPTLNTWTQKLTDRLRGNPAFRDISNDLQLGGSITHINIDRSAAARFGLTASDVDQALYDAFGQRQINEFQTETNQYNVILELDTAQRGRAESLAYFYLRSPLSGEMVPLSALARFDAPTNGPLSIAHDGMFPAANLSFNLAPGVALGDAVRMLDQAKNEVGMPASITGNFQGAAQAFQSSLASQPWLILAALLAVYIILGVLYESFVHPLTIISTLPSAGLGALVMLWLLGQDFSIMALIGLVLLIGIVKKNGILMIDFALDAQRKGGLTPQEAIFQACLTRFRPIIMTTLAALLGALPLMLGSGPGAELRQPLGIAVVGGLLVSQALTLFTTPVIYLWLERLFHRPVQQPGPAPTTLATTD
>NZ_CP054128.1|WP_173406581.1|1437131_1438289_-|efflux-RND-transporter-periplasmic-adaptor-subunit
MHIQKKTVLLVALLVALAAVALWYVMKPVTAKPGAPVAVPVRVISVVQKDVPRFASGIGTVLSLHSVVIRPQIDGILTQLLVKEGQQVKKGELLATIDDRSIRASLDQARAQLGESQAQLAVAQVNLKRYKLLSVDDGVSKQTYDQQQALVNQLKATAQGNQAAIDAAQVQLSYTRIRSPVTGRVGIRNVDEGNFLRTSDTEGLFTVTQIDPIAVEFALPQQMLPTLQRLMAAPEQALVQAYIGADGTSGEMLGEGRLSLIDNQINANTGTLRAKAEFSNAAQRLWPGQLVTLKIQTALDKDALVVPPTVVQRGLEQPFVYRITGDRVESVPVVMVYQDSDLHIIKGVSAGDQLVSDGQSRLKPGSRIQVLGDPVAQANVSEPKP
>NZ_CP054128.1|WP_047228828.1|1438525_1438780_+|hypothetical-protein
MTSPTPSPADERPNGEQADRPDSDVSSGESVNAIPTFKFPFKPGELAAAKGAGQQPWYKNGAKNGHTKTPGAAPPGTRRSMGKR
>NZ_CP054128.1|WP_047228829.1|1438807_1439776_-|LysR-family-transcriptional-regulator
MDTLQNMRAFSCVAEAGSFTAAAVQLDTTTANVSRAVSNLEAHLQTRLLNRTTRRIALTEAGKRYLLRCEQILAYVEEAEAEASDAHARPAGQLKVHTMTGIGQHFVIDAIARYRKTHPDVTFDLTLANRVPDILDEGYDVSIVLASELPDSGFVSQRLGITYSIVCASPAYVKASGCPQKPGDLLNHACLRLVSPVIPLEKWVFDGPEGQEMVTISNSPFLVNSADAMKTAITSGMGVGVLPVYAAIEGLRNGTLVRVMPNYRSQELNLYAIYPSRQYLDAKIKTWVEYLRGSLPEILAAHQAELTAYELSGSLAGARVAN
>NZ_CP054128.1|WP_047228830.1|1440087_1441560_+|efflux-transporter-outer-membrane-subunit
MPRCISRELKTLSVWLLTFTISGCIGTGGIAPQGQALSANQLATDEAIREAARDAHWPTGQWWNAYGDRQLDRWIDLAVHDSPSLALAAARVRQAKAMAGVVEAAESLQINGQATLKRHNWPTDQFYGPGELADTTTWDNNAGLGLSYALDLWGRERNASERAVDLAHVSVAEARQAQLELQNNIVRTYIQFALHYAQRDIVVATLHQQEQILELAQKRLDGGIGTHFEVSQAQAPLPETHRQLDALDEAIALSRNQLAALAGKGPGDGARLQRPTLALGAPLKLPSALPAELLGQRPDVVAGRWQVAAQARGIDVARAGFYPNVDLVGSIGYMATGGGALEFLTGKKLNYSVGPAITLPIFDGGRLRSQLGEAAAGYDIAVAHYNQTLVDALKSISDQLIRRESMDKQHVFAAESVAAAQRTYDIAMVAFQRGLTDYLNVLNAQSLLFKQQQVQQQVEAARLTAHADLVTALGGGLDAGKDIPDLSHVE
>NZ_CP054128.1|WP_173406582.1|1441567_1443760_+|FUSC-family-protein
MMSLCAPARWLYRLEWRRGFFDWARSDGVTWVYIFKVLLAAFLTLWLAMRLELPQPRTAMITVFIVMQPQSGQVFAKSFYRLLGTLAGSAVMVALIALFAQNTELFLGSLAIWVGVCSAGAARYRNFRAYGFVLAGYTAAMIGLPALAHPEGAFMAAVWRVLEISLGILCATLISAAILPQTASAAMRNALYQRFGVFALFVTDGLRGRSKREAFEARNVGFIAEAVGLESLRSVTVFEDPHMRRRNGRLSRLNSEFMGITTRFNALHQLLERLRSRGVDHVVNAIKPGLLTLAELLDGFSARALTDKDAARLAAELATYKADLPAQVRTLRGVFEETDPSEAERLDFHTAYELLYRFVDDLHGYAQTHASLADHRHEREQWDQPFMPQTNGLAAAASGFRAAFILLVLGSYWVATAWPSGATMTMIAAATVGLSAATPNPKRMAFQMACGTLLGALIGFVEMFFIFPLIDGFPLLCVMLAPVIMLGSFLSSRPQYAGVGLGLLIFFCTGSVPDNLTVYNPYTFINDYLAMILGMLVCAAAGAIILPPNSRWLWRRLEQDLREQVVFAISGRLKGLASGFESRTRDLLHQAYGLAAGQPGVQRDLLRWMFVVLEVGHAIIELRKEQAILPVHPAYAPSQPWRQAIRVMGRALVRLFRQPGQSNLERALLAVDHAISRVQASDEPFAPHFDTSALRRVKSYLHFIRTSLLDPQSPLAAYARPLPQEPEHAS
>NZ_CP054128.1|WP_024617598.1|1443749_1443950_+|DUF1656-domain-containing-protein
MPREIAFHGVYMPTMTLMFFIAAALAWALDRFLSGLDLYRFFWHPALLRLSLFTCLFGALALTVYR

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Crispr_ID: NZ_CP054128_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP054128_2

2262826-2262919

Orphan

Consensus_repeat	Method
TGTGGGAGCGAGCCTGCTCGCGAT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP054128_2

>merge|NZ_CP054128|2|2262826-2262919|CRISPRCasFinder
TGTGGGAGCGAGCCTGCTCGCGATAGCGGTCTGACGGTCGACCGATCTCTCGCGGATGTACCAGATCCATTGTGGGAGCGAGCCTGCTCGCGAT

>NZ_CP054128|2|2|2262826-2262919|CRISPRCasFinder
TGTGGGAGCGAGCCTGCTCGCGAT	AGCGGTCTGACGGTCGACCGATCTCTCGCGGATGTACCAGATCCAT
TGTGGGAGCGAGCCTGCTCGCGAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP054128.1\|WP_173406739.1\|2272382_2275667_+\|transporter-substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|270423
NZ_CP054128.1\|WP_160891252.1\|2263008_2264625_+\|PvdJ/PvdD/PvdP-like-protein	unknown	unknown	unknown
NZ_CP054128.1\|WP_047229284.1\|2275795_2276230_+\|chemotaxis-protein-CheY	unknown	unknown	unknown
NZ_CP054128.1\|WP_173406738.1\|2270850_2272185_+\|SidA/IucD/PvdA-family-monooxygenase	unknown	unknown	gnl\|CDD\|226017
NZ_CP054128.1\|WP_173406731.1\|2253077_2257235_-\|amino-acid-adenylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|237108
NZ_CP054128.1\|WP_173406736.1\|2266632_2268603_-\|MacB-family-efflux-pump-subunit	unknown	unknown	gnl\|CDD\|182528
NZ_CP054128.1\|WP_173406728.1\|2220072_2232423_+\|non-ribosomal-peptide-synthase/polyketide-synthase	unknown	unknown	gnl\|CDD\|237054
NZ_CP054128.1\|WP_047229292.1\|2260046_2261327_-\|aminotransferase-class-V-fold-PLP-dependent-enzyme	unknown	unknown	gnl\|CDD\|223594
NZ_CP054128.1\|WP_173406735.1\|2265227_2266622_-\|efflux-transporter-outer-membrane-subunit	unknown	unknown	gnl\|CDD\|273830
NZ_CP054128.1\|WP_173406737.1\|2270222_2270705_+\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|171560
NZ_CP054128.1\|WP_173406730.1\|2246074_2249305_+\|amino-acid-adenylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|341253
NZ_CP054128.1\|WP_173406729.1\|2232422_2246078_+\|non-ribosomal-peptide-synthase/polyketide-synthase	unknown	unknown	gnl\|CDD\|237108
NZ_CP054128.1\|WP_172833789.1\|2276306_2276960_+\|response-regulator	unknown	unknown	gnl\|CDD\|225107
NZ_CP054128.1\|WP_173406734.1\|2261323_2262694_-\|pyoverdine-tailoring-dipeptidase-like-protein-PvdM	unknown	unknown	gnl\|CDD\|366534
NZ_CP054128.1\|WP_076383897.1\|2268603_2269755_-\|efflux-RND-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|183211
NZ_CP054128.1\|WP_047229282.1\|2277140_2278007_+\|pirin-family-protein	unknown	unknown	gnl\|CDD\|224655
NZ_CP054128.1\|WP_047230459.1\|2219074_2219809_+\|thioesterase	unknown	unknown	gnl\|CDD\|225749
NZ_CP054128.1\|WP_076383888.1\|2249798_2252267_+\|TonB-dependent-siderophore-receptor	unknown	unknown	gnl\|CDD\|227114
NZ_CP054128.1\|WP_173406732.1\|2257249_2258908_-\|cyclic-peptide-export-ABC-transporter	unknown	unknown	gnl\|CDD\|130262
NZ_CP054128.1\|WP_173406733.1\|2259146_2260022_-\|formylglycine-generating-enzyme-family-protein	unknown	unknown	gnl\|CDD\|335469

Protein	Function_ID	Function_description	E-value
NZ_CP054128.1\|WP_173406739.1\|2272382_2275667_+\|transporter-substrate-binding-domain-containing-protein	gnl\|CDD\|270423	cd13705, PBP2_BvgS_D1, The first of the two tandem periplasmic domains of sensor-kinase BvgS; the type 2 peripasmic-binding fold protein. This group contains the first domain of the periplasmic solute-binding domains of BvgS and related proteins. BvgS is composed of two periplasmic domains homologous to bacterial periplasmic-binding proteins (PBPs), a transmembrane region followed successively by a cytoplasmic PAS (Per/ARNT/SIM), a histidine-kinase (HK), a receiver and a histidine phosphotransfer (Hpt) domains. The sensor protein BvgS can autophosphorylate and phosphorylate the response regulator BvgA. The BvgAS phosphorelay controls the expression of virulence factors in response to certain environmental stimuli in Bordetella pertussis. Its close homologs, Escherichia coli EvgS and Klebsiella pneumoniae KvgS, appear to be involved in the transcriptional regulation of drug efflux pumps and in countering free radical stresses and sensing iron limiting conditions, respectively. The periplasmic sensor domain of BvgS belongs to the type 2 periplasmic-binding fold protein (PBP2) superfamily, whose members are involved in chemotaxis and uptake of nutrients and other small molecules from the extracellular space as a primary receptor. PBP2 typically comprises of two globular subdomains connected by a flexible hinge and 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 receptor cytoplasmically-located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	2.54876e-99
NZ_CP054128.1\|WP_076383888.1\|2249798_2252267_+\|TonB-dependent-siderophore-receptor	gnl\|CDD\|227114	COG4773, FhuE, Outer membrane receptor for ferric coprogen and ferric-rhodotorulic acid [Inorganic ion transport and metabolism].	0
NZ_CP054128.1\|WP_173406738.1\|2270850_2272185_+\|SidA/IucD/PvdA-family-monooxygenase	gnl\|CDD\|226017	COG3486, IucD, Lysine/ornithine N-monooxygenase [Secondary metabolites biosynthesis, transport, and catabolism].	6.02325e-165
NZ_CP054128.1\|WP_173406731.1\|2253077_2257235_-\|amino-acid-adenylation-domain-containing-protein	gnl\|CDD\|237108	PRK12467, PRK12467, peptide synthase; Provisional.	0
NZ_CP054128.1\|WP_173406736.1\|2266632_2268603_-\|MacB-family-efflux-pump-subunit	gnl\|CDD\|182528	PRK10535, PRK10535, macrolide ABC transporter ATP-binding protein/permease MacB.	0
NZ_CP054128.1\|WP_047229292.1\|2260046_2261327_-\|aminotransferase-class-V-fold-PLP-dependent-enzyme	gnl\|CDD\|223594	COG0520, csdA, Selenocysteine lyase/Cysteine desulfurase [Posttranslational modification, protein turnover, chaperones].	2.5978e-58
NZ_CP054128.1\|WP_173406735.1\|2265227_2266622_-\|efflux-transporter-outer-membrane-subunit	gnl\|CDD\|273830	TIGR01845, Outer_membrane_protein_OprM, efflux transporter, outer membrane factor (OMF) lipoprotein, NodT family. Members of this model comprise a subfamily of the Outer Membrane Factor (TCDB 1.B.17) porins. OMF proteins operate in conjunction with a primary transporter of the RND, MFS, ABC, or PET systems, and a MFP (membrane fusion protein) to tranport substrates across membranes. The complex thus formed allows transport (export) of various solutes (heavy metal cations; drugs, oligosaccharides, proteins, etc.) across the two envelopes of the Gram-negative bacterial cell envelope in a single energy-coupled step. Current data suggest that the OMF (and not the MFP) is largely responsible for the formation of both the trans-outer membrane and trans-periplasmic channels. The roles played by the MFP have yet to be determined. [Cellular processes, Detoxification, Transport and binding proteins, Porins].	9.45035e-87
NZ_CP054128.1\|WP_173406737.1\|2270222_2270705_+\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|171560	PRK12527, PRK12527, RNA polymerase sigma factor; Reviewed.	6.22389e-98
NZ_CP054128.1\|WP_173406730.1\|2246074_2249305_+\|amino-acid-adenylation-domain-containing-protein	gnl\|CDD\|341253	cd05930, A_NRPS, The adenylation domain of nonribosomal peptide synthetases (NRPS). The adenylation (A) domain of NRPS recognizes a specific amino acid or hydroxy acid and activates it as an (amino) acyl adenylate by hydrolysis of ATP. The activated acyl moiety then forms a thioester bond to the enzyme-bound cofactor phosphopantetheine of a peptidyl carrier protein domain. NRPSs are large multifunctional enzymes which synthesize many therapeutically useful peptides in bacteria and fungi via a template-directed, nucleic acid independent nonribosomal mechanism. These natural products include antibiotics, immunosuppressants, plant and animal toxins, and enzyme inhibitors. NRPS has a distinct modular structure in which each module is responsible for the recognition, activation, and in some cases, modification of a single amino acid residue of the final peptide product. The modules can be subdivided into domains that catalyze specific biochemical reactions.	3.49563e-162
NZ_CP054128.1\|WP_173406729.1\|2232422_2246078_+\|non-ribosomal-peptide-synthase/polyketide-synthase	gnl\|CDD\|237108	PRK12467, PRK12467, peptide synthase; Provisional.	0
NZ_CP054128.1\|WP_172833789.1\|2276306_2276960_+\|response-regulator	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	7.62208e-57
NZ_CP054128.1\|WP_173406734.1\|2261323_2262694_-\|pyoverdine-tailoring-dipeptidase-like-protein-PvdM	gnl\|CDD\|366534	pfam01244, Peptidase_M19, Membrane dipeptidase (Peptidase family M19).	1.75599e-106
NZ_CP054128.1\|WP_076383897.1\|2268603_2269755_-\|efflux-RND-transporter-periplasmic-adaptor-subunit	gnl\|CDD\|183211	PRK11578, PRK11578, macrolide transporter subunit MacA; Provisional.	3.62898e-78
NZ_CP054128.1\|WP_047229282.1\|2277140_2278007_+\|pirin-family-protein	gnl\|CDD\|224655	COG1741, COG1741, Pirin-related protein [General function prediction only].	4.51702e-88
NZ_CP054128.1\|WP_047230459.1\|2219074_2219809_+\|thioesterase	gnl\|CDD\|225749	COG3208, GrsT, Predicted thioesterase involved in non-ribosomal peptide biosynthesis [Secondary metabolites biosynthesis, transport, and catabolism].	3.89036e-82
NZ_CP054128.1\|WP_173406728.1\|2220072_2232423_+\|non-ribosomal-peptide-synthase/polyketide-synthase	gnl\|CDD\|237054	PRK12316, PRK12316, peptide synthase; Provisional.	0
NZ_CP054128.1\|WP_173406732.1\|2257249_2258908_-\|cyclic-peptide-export-ABC-transporter	gnl\|CDD\|130262	TIGR01194, ATP-binding_protein_SyrD, cyclic peptide transporter. This model describes cyclic peptide transporter in bacteria. Bacteria have elaborate pathways for the production of toxins and secondary metabolites. Many such compounds, including syringomycin and pyoverdine are synthesized on non-ribosomal templates consisting of a multienzyme complex. On several occasions the proteins of the complex and transporter protein are present on the same operon. Often times these compounds cross the biological membrane by specific transporters. Syringomycin is an amphipathic, cylclic lipodepsipeptide when inserted into host causes formation of channels, permeable to variety of cations. On the other hand, pyoverdine is a cyclic octa-peptidyl dihydroxyquinoline, which is efficient in sequestering iron for uptake. [Transport and binding proteins, Amino acids, peptides and amines, Transport and binding proteins, Other].	0
NZ_CP054128.1\|WP_173406733.1\|2259146_2260022_-\|formylglycine-generating-enzyme-family-protein	gnl\|CDD\|335469	pfam03781, FGE-sulfatase, Sulfatase-modifying factor enzyme 1. This domain is found in eukaryotic proteins required for post-translational sulfatase modification (SUMF1). These proteins are associated with the rare disorder multiple sulfatase deficiency (MSD). The protein product of the SUMF1 gene is FGE, formylglycine (FGly),-generating enzyme, which is a sulfatase. Sulfatases are enzymes essential for degradation and remodelling of sulfate esters, and formylglycine (FGly), the key catalytic in the active site, is unique to sulfatases. FGE is localized to the endoplasmic reticulum (ER) and interacts with and modifies the unfolded form of newly synthesized sulfatases. FGE is a single-domain monomer with a surprising paucity of secondary structure that adopts a unique fold which is stabilized by two Ca2+ ions. The effect of all mutations found in MSD patients is explained by the FGE structure, providing a molecular basis for MSD. A redox-active disulfide bond is present in the active site of FGE. An oxidized cysteine residue, possibly cysteine sulfenic acid, has been detected that may allow formulation of a structure-based mechanism for FGly formation from cysteine residues in all sulfatases. In Mycobacteria and Treponema denticola this enzyme functions as an iron(II)-dependent oxidoreductase.	9.74844e-66

>NZ_CP054128.1|WP_173406734.1|2261323_2262694_-|pyoverdine-tailoring-dipeptidase-like-protein-PvdM
MTTPRSKKALFIGVPLALALAVGGGLTAWDHWWRDNPGYPVKVMKEARELHERLLSFDSHISVPLNFGTAGHEADKDGKGQFDLVKANRGHLSGAALTIFGWPELWNGPNAPHKPTAGFVEEARNQQEVRFKIITGMVRDFPNQVAIAYTPDDFRRLHGEGKFAIFISMLNAYPLGHDLSLLDLWTARGMRMFGFSYIGNNDWADSSRPLPFFNDSPDALGGLSDIGKQAVTRLNDLGVIIDVSQMSTQALEQVAQLSRTPLVASHSAPRAMVDIPRNLSDKEMQLIKASGGVVQVVGFSQYLRPLTQKTQDKLNDLRKRFDLPPLPNLAMALMPGDPIIAAWPEQKFGEYAGQLYGILEEEPKASLKDLGDAIDYTVRKIGIDHVGISSDFNEGGGVKGWEDVGEIRNVTAELLTRGYSEADIAKLWGGNFLRVWDQVQQAARPAVASTRGAVQP
>NZ_CP054128.1|WP_047229292.1|2260046_2261327_-|aminotransferase-class-V-fold-PLP-dependent-enzyme
MNERRTFLKHAGILAAGLPLAASLPAPAIADPLPPLPRDKWAQLRSLFNQDPDYLHFSNFLVTTHPRPVREAIDRHRAALDKNPGLLMDWDLGVTEEREENVRTWAGRYLQATPKQIALTGSTTEGLSIIYGGVHVAADQEILSTAHEHYATHTILDLRNQRDGTRVRKIKLFENAHNASHDDILSAIDRNIRPETRVLGMTWVHSGSGVKLPIDKIGALVDKHNQGRSDTQRIIYVVDGVHGFGVEDLSFPAMNCDFFIAGTHKWMFGPRGTGLVCSRSEELKYVTPIIPTFSEATAFSTTMTPGGYHAFEHRWAADEAFKLHLQLGKADVQARIHALNTYLKKQLLALPQIELVTPMSPDVSAGFTFFRVKGRKSDEIAAYLMQNRVIADAVHRDAGPVIRTAPGLLNTEAEIDRFMGLLGKTL
>NZ_CP054128.1|WP_173406733.1|2259146_2260022_-|formylglycine-generating-enzyme-family-protein
MNSFSLKLFPALALAALLPSGAQASQPGQVFRDCKDCPEMVVLPTGTFQMGTPEDEVGREPDEGPMHPVTFAKPLAISRFQVLKGEWFAYLRDTGYSMPDGDKRPGRACKAGIPDYQGSDPRKQYTDRHPAVCMNFEEANAYVAWLSKKTGKPYRLVSESLREYAARGGSTGPFPFPFDEGKEYSIAQHANTYGAADGYNFTAPAGSFAPNAFGVYDMHGNVYEWTADCYNENYVGAPSDGSAWLTGKCEFKRIRGNDWGEAPVFSRSGNRNALVPGNRGDWIGFRVARDM
>NZ_CP054128.1|WP_173406732.1|2257249_2258908_-|cyclic-peptide-export-ABC-transporter
MSQPTRGVINELFILLKPFRLIVVGSILLGMLGGLSITALLATINDALNAAAKPTAQTLVTFVVLCAVALLTSILSDIGSNHVGQNIIAGLRKSLGKKVLLAPIEQIERYRSHRLIPVLTHDVNTVSNFAFSFAPLAIAFTVTLGCLGYLAYLSLPMFLLLLVALVIGTVVQYLARARGIRGFEAAREAEDALQKHYSAIAAGAKELRIHRPRRQRMFSQRIEATADNICDTNIRAVNTFVVAKTFGSMLFFVVIGLVLALQSLWLGTDKAVLSGFVLVLLYMKGPLEYLVMTLPVISRANIAFKRIAELDEQFSSPEPHLLLDDKSLSRPALQQLELRDVHYAFPAVEGSQPFALGPINLSIAQGDIVFIVGENGGGKTTLIKLLLGLYFPQGGEILLDGAPVGAAQRDDYRQLFTTIFADYYLFDDLVQGDQQVPDDANRYLERLEIAHKVRIQDGAFSTTDLSTGQRKRLALLNAWLEERPVLVFDEWAADQDPVFRRVFYTELLPELKALGKTIIVISHDDRYFDIADQLVRMQAGQVISEKAPAAFA
>NZ_CP054128.1|WP_173406731.1|2253077_2257235_-|amino-acid-adenylation-domain-containing-protein
MNPLLDDDLLTLLLEEDADAVQARSSRSRPDRAPLSFAQQRLWLEQQRDPSRSAYNLPRALRLTGELNADALERALNRVIDRHDILRTAFTEIDGAATQVIERNASLIVHRENLAALDQPTRELALSQRIEQHARQPFDLTQAPLMRATLLRLGSDEHVLLLNMHHIVSDAWSNTILMQDMTMAYAQALLGDPSTLPSLPLQYADYASWQRGDYVQSPACHRSGAYWSDYLGHELPALELPQEFARTANQQHMAGRVQVSLDPAMVQALDTFCQREGLTPFVVALAAWQLLLARYSNQNDFTVGVPNANRNSHESQELVGFFVSSQVYRARIDSTRSALDFLRDLRAQSLAALEHADYPLELILDQLQRPGAQGASALFQVLFNWRTGSSSPSAPNLGQLTLEFLNTGDNQAKFDLSLDVDYSQQQLLATFEYSRDLYRAETIERMAGHWQNLLRGLVETTGCALGELQLLSADEHRKTLGDWNRQPTQLRSEQCLHRLIETHAASTGDAIALTFEGQHMSYAELNRQANQLAHRLIEQGVGPDVLVGIAVERTPQMIIGLLAILKAGGAYVPLDPAYPADRLAYMIADSGVTQILTQAHLRESLALPADINCLLLDSVDTNSPYPEHNPNVPMDPDNLAYVIYTSGSTGQPKGALLAHHNVSRLFQATDHWFSFDHQDVWCLFHSYAFDFSVWEIFGALLHGGRLVIVPHAVSRSPQDFYALVCQENVTVLNQTPSAFKALLQVACEPGQPLAHRLRQVIFGGEAIDVQSLRPWFERFGDQTPQLINMYGITETTVHVTWRPLSMSDLHSEAASPIGEPIVDLSWYLLDAHLNPVPKGCIGELYVGRAGLARGYHRRADLTATRFIPDPFDPLPGGRLYRTGDLARYRTDGSIEYIGRLDHQVKIRGFRIELGEIQARLQTLPAVQDGVVLTHEGPGGLQLVAYVIAAQPATAELREGLLSALKAQLPDYMVPSHLLFIDHFPLNANGKLDRKALPEPDAGLWHSLYLAPRTQLEEALAQLWQQSLKVARVGVNDSFFELGGHSILAIELIANLKARLNISVRLQELLANPSVAELALFISQKHREQTQCLVELNNAPASAPQLFCLHPSGGIVFCYQPLARKLQQRARTVGVMHRGFSEPHAGPEAWGEMIADYSQEIVKAQPQGPYYLMGWSLGGAIALDIAATLESLGHTVSFLGLVDSTVPEPLYPATLSRHRHLPGAEQADPASQDLLEAIEYFDLLFPTLTERTATYRREQPESTVKAFHEWAASQIEPGRGDLLAIVQSVKDEVMNAQAFSVHDRLLEAFDGFTFKPVRVRPSCWWTQVEKNPEELAFCEALIKSYSLTGELQCSMHSPLRHRSMIFDDGLLDSLVEAFWASTIEGE
>NZ_CP054128.1|WP_076383888.1|2249798_2252267_+|TonB-dependent-siderophore-receptor
MSSIHELKPLFKALVMSRGLRSRRVLTGLGLVCLLPLSAQVMAEDVSVDIPAQSLPQALQAFGQQTNQQVIYNAGDMAGLKSNRVSGKMSPQAALTELLKGTGVRYSVEGNTLMLLRGSATGSLELGATTVKAQELVATTEGSKSYTSNAVTIGKGTHTLKEIPQSITVMTRKQMDDQNLVNLKDAVNQTTGIVGLQGVGQGMILSSRGFQIDDWQYDGVPILRNNYSLGNWATQDLIFFDRLEIMRGASGLLQGTGSPGGAVNLVRKRGQNAPTVTLTGKAGSWDHYGLQLDAGGPLNQAGNIRGRIVVDEDQSNSFVDHAWSKTHSLYGALDVDLSEDTTLGFAVSQSNGESRGNIRGLPRYADGRMPDVSRSTYTGARWNRSEIDVTTLYADLEHRFNEDWAFKVGAVHMSEDNQAKNQRVQRGGGLLPDGSGVQYADFLTDFQSTKAGLDMNLTGKFEALSMEQEVMLGGNYSQLETDDRYARTFNNTSDSIFDIDNDRPDISYDSLIAAGGQGTLSKYDIRQKGVYGTWRVKPVDDLTLVLGSRVSWYDYSYKSKTENSAGITGNAPSTGTETGVVTPYAGIIYDLSREWAVYASYTDVFQPQTNRDANGSVLKPIVGTNYEVGLKGELMDGRVNTSLAIFRYDHENRAINDGGSGCGGSGCSVASGKVRSQGIDAEISGEVIDNLQLFAGYTYNTTKYLEDPDNEGSIFSTWTPKHMLRVWGNYQFTGDWSRVSTGLGFTSQSHTMVYDYDREVPGYTVWNARVGYQLTSEIALAVNANNLFDKTYITSAYNQLNGNNNFGDPRNLMFSVTYKPQF
>NZ_CP054128.1|WP_173406730.1|2246074_2249305_+|amino-acid-adenylation-domain-containing-protein
MNEVLMDQQDPGFALTPEQQAMLEQLSSTATCGEALRWLNVVIDGDLDPQRLQIAFDTLLAQQPMLLARLDKVAGFHGLRQVASGAARFPLTIQAGEQRTEDVQAQIKDSLGCAFVVGESPNVQAVLYRLAPQQWQLVLGIARYSADAQSLNLLLEQVQQAYAAVQASEDEAPGEFAQYLEWRSEVVLDEDAATGRTYWQHYLQGVQTDIATPWLAARSAGSETGAADTCVSLTLEPAQRDGLQRLAEQLDQPLATLLQGAWWVLLGRLSGLEQALVGVRHDSRGDYEYFANAVGVFEKTLPLSVSLPATVSFSEWLDELAARLEAHRTWQEYWAPELSPEAARPAYGFTLGQANRAGNSGGLNWAVAESVRVPADPFELLLQVQLNAAQQLAAVNLHYASSRYSPASASAVLEQYGVLLASILAAPHTALARLDLLSRTAEQRLLAINPAMHALADGRYLPQRIADLASHTPNAIALTGARQQMSYGQLQARVDSMAQGLKQQGVGAGSMVALALPRSVDLVIAMLASWRLGAAYLPLDVQWPQARQALMLEQAGAALLLTDAAHLPAWQDQPYKALTAAELSHPATPLPALATQGNDIAYVLFTSGSTGVPKGVVIEHRQLLNYTAQASQALGLAQCKNVGFSSSVAADLGNTALFGALFNGATLHVASDEQMQDGVLFAQYLQQQQIDCLKIVPSHLAALLDGERALLPGTLVLGGEPIAPTLVERIARLRSDCRVFNHYGPTEATVGVMIHPLSLNGAAGDCSALTQVLGNNQVYVLDADLRLAPVGVLGEVYLGGAQLCRGYLNAEADAQAFIQSPFDPAQRLYRTGDLARYRPDGAIQLYGRRDQQVKVRGFRIELAEIEAVLVRMPQVAEALVLPAASAEQGLLAFVVAQQGPLTGLLDAARAELSARLPSVMVPQHVHLIERFPRLANGKIDRHALQQLAVATADDEDAAPRDALEQLLAARMAQLLGLERLGIDRDFFAAGGHSLLVIKLVAGIRKLLQCEIHPGLVFDHPTVASLALALRALESSPGQLEKMAQVRLRMEAMSPEEKALLTEQARQLQAAKAAQGS
>NZ_CP054128.1|WP_173406729.1|2232422_2246078_+|non-ribosomal-peptide-synthase/polyketide-synthase
MDKSVALTIAKRFITLPLDKRKLYLEKMLEEGVSPANLPIPQVRLGFEHIPLSYAQERQWFLWQMDPHSSAYHIPSALRLKGQLDVPALERSFNALLERHESLRTTFGENGEQTVQVIHRHMPLGIAVQALTAAPSASEDDAIKAFVEAETARPFDLRQGPLLRVSLLKIAEDDHVLALIQHHIIADGWSMQVLVDELVRHYAADTAGQPLALPALSVQYADYAIWQRHWLEAGERERQLAYWVQTLGDEQPVLELPLDHPRPPVQSFRGARLDLNLPPELGAALKQLAQREGASLFMVLLASFQALLHRYSGQPQIRVGVPVANRNRVETEGLIGFFVNTQVLNAHVDGQLPFDRLLAQVKQSAMAAQAHQDLPFEQLIEALQPERSLSHSPIFQVMFNHQTASDTQDRQQQLPHLSVEDLVWEGRTAQFDLTLGTYETGQGVAAELTYATDLFEPHTIERLARHWQNLLQGIVDAPQQRIGELPLLDTAQQRRTQQDWHRVVDHGSDALCVHQRIAEQARITPDALALSIDGQALSYGQLEARANQLAQRLIGLGVTPDQPVGIAVQRSAEMLVGLLAILKAGGAYVPLDPAYPEDRLAYMIQDSGIELLLTQARLQAQLPIPATLRTLLLDQPDAAWQAAPSTCPAVPLTAEHLAYVIYTSGSTGKPKGVMVRHGALSNFVTSMIARPGITASDRMLSLTTFSFDIFGLEIYGPLSAGASVVLTGQDVHQDPQAVLALIERHDVSVLQATPSSWRMLLDHEHSAVLAGRTFLCGGEALPLELAQRLLALSPKVWNLYGPTETTIWSAVHPLSLENSRPFLGKPLDNTALYIVGSDLTLNPPGAPGELLIGGDGLARGYFQRPALTAERFVPDPFSTCGERLYRTGDLTRYRAEGVVEYIGRIDHQVKIRGLRIELGEIEAALLAQDTVRETVVVAHEAPTGAQLVGYVVPATGEAADEASLRASLKAALKAQLPEYMVPAHLVFLAQLPLTPNGKVDRKALPAPDVGEVQRRYVAPRSQREQQVAAIWQEVLKLERVGLEDNFFELGGHSLLVTQVVSRVRRALAIEVPLRSLFEHSTLQDFVNALDAGQGELAPAMVPVSRDAPLPLSFAQERQWFLWKMDPNSAAYNIPTALRMHGALDKIALRQSFEALLQRHESLRTAFVEDDGRTCQVIRPQGQVHFVEQRLAVADEASIQAFLEQQTQRPFDLLSEALLRVALLELSEQEHILVLTVHHIVADAWSLQVMVDDLMSLYSAFIQEQPAQLPPLAVQYADYAVWQRQWMAAGERERQLAYWTGQLGSEQPLLELPTDHPRPAQQSLRGARLPIVLDRSLSDALKALARRENVTLFVLLLGSFQALLHRYSGQADIRVGVPIANRHRLETERLIGFFVNTQVLRAEFHRDLTGADLLQQLKQTAMAAQMHQDLPFEQLVDALQPQRNLSHSPLFQAMFNHRNETGAALANALPGLAVEPLGWEQRTAQFDLSLDTSDSPQGLHAALTYATDLFEPATIERMGRHWLNLLQGLVQDLHRPVAQWALLDADERRRMLLDWNATTAQYPLDRSVHGLIEEQVRRTPDAPALVFGEQRLTYAQLNARANRLAHRLIEQGVGPDVLVGIAVERSVEMVLGLLAILKAGGAYVPLDPEYPRERLAYMFEDSGIGLLLTQSHLLEQLPIPPGLRSLVLDLPDDGLQAGRDTNPHVKLDGENLAYVIYTSGSTGKPKGAGNRHSALVNRLCWMQDAYRLEADDSVLQKTPFSFDVSVWEFFWPLLTGSTLVVAAPGAHRDPTQLIELITAQRITTLHFVPSMLQAFLQDPHVAECTSLKRIVCSGEALPVDAQQQVFAKLPNAGLYNLYGPTEAAIDVTHWTCVEEGRDSVPIGQPIANLGTCILDDELSPVPVGVIGELYLAGEGLARGYHRRPALTAERFVTGPFGNGQRLYRTGDLARYRADGVIEYAGRMDHQVKIRGLRIELGEIEARLAEHDDVREAVVIAQDGSLLVAYVVPARAELLTAEDIVRQTLQGHLKEHLSQALPDYMVPQHWLWLEEMPVSPNGKLERKALPKADITANPKAYIAPVTAIEQALAGIWQSVLGRGQVGLSDNFFELGGDSIVSIQMVSRARQAGIHFSPKDLFIHQTIQGLASVATLGDSGLAIDQGPVTGETLLLPFQQWFFDQPMAEPHHWNQSVLLKGLRPLHAGHLEQALQALVAHHDALRLAFRREDDAWTARHQTLAEQQANWRRSPLLWTAEVADAPALERLAEQAQRSLDLESGALLRGVLANLADGSQRLLLVIHHMVVDGVSWRILLEDLQQAYEQLQAGQTPKLPAKTSATQAWAQRLKTHAGSAAFQTQMAYWQGQLEGARGDLPCDRPQGELRRCHGAQVQTRLDKNQTRQLLQQAPAAYRTQVNDLLLTALAQVIGRWTGEASTLIQLEGHGREALFDDLDLSRSVGWFTSLFPVRLTPATTTEDSIKAIKEQLRAIPDKGLGFAVLRYLGDEPTRCALQALPVPRITFNYLGQFDSGFADDAAGLFVPAGESAGAPQSPLAPLDNWLTLNGSVYAGELSIDWTFSTQMFDESTIQALALDYAQELQALIEHCCQTRHQGFTPSDFPLAGLTQAQLDTLPLAARQIEDIYPLSPMQQGMLFHTLYEQQAGNYINQLRVDVAGLDVERFRQAWQAAMDTHEVLRSSFVWDGDFKRALQVVHKQMEVAFLFHDGGAAANPSQDLDALALAQREQGFELDAAPLLRLLVVRVAEDRYHLIYTSHHILMDGWSNSQLLGEVLQRYSSQPVVASGSRYRDYIAWLQRQDGAASEAFWKPALQRLEAPTRLADAVASPTQTGAGYGDHVQVLDETLTRRLEAFARASKVTVNTLVQAAWLLLLQRYTGKDTVAFGATVAGRPADLPGIEQQIGLFINTLPVIASPRAEQSLDSWLQAVQAQNLALREFEHTALLDIQRWAGQGGEALFDSLLVFENYPIAQALEQGAPDGLRFGPAATQEQTNYPLTLLVGLDRQLSVHMSYQRASFEPATVTRLATHLAQLLGQMTDGGERCLSELSMLEFDEHQRLTHDWNPLDAPFEQNLCIHQMIARQAEATPDALAVTFANTRLSYSEVDGRANRLAHQLIEMGVGPEVRVGVAMPRSEHLLIALLAVLKAGGAYVPLDPDYPAERLAYMLDDSRARVLLTEQSVAATLSVPAETAVLMLDQLDLAHHPLSAPRTTVTPDNLAYVIYTSGSTGQPKGVAIAHRNVLALIDWSRSVYSHDDIQGVLASTSVCFDLSVWELFVTLANGGSLIIARNALELPQLPTRDQVRLINSVPSAIAALQRSGEIPASVRIINLAGEPLKQSLVDALYQHPIGGSEPVEAKPVGTEPVGAKLARDSILSAGPCVTDPPPSRASFAPTDCASTGVLPQGIEHVYDLYGPSEDTTYSTWTRRTAGGTANIGRPVKHTASYLLDADLQAVPQGVSAELYLSGAGITRGYLGRAAMTAEKYVPNPFSTTGERLYRTGDLSRYRADGVLEYQGRIDHQVKIRGFRIELGEIEARLLQQPQVHDVAVLAQDAPGGQQLVAYVVASALQADESSARAQLKAGLKEHLPDYMIPTHLLFLEHLPLTPNGKLDRKALPAVDTGLSQSGYEAPEGELEQQIAGVWQEVLELEQVGRNDHFFERGGHSLLATQAVSRLRKLTGYPLSLRDLFDHPQLKALAALMAGTVDGPVRAGDSRGVRLQAHGPRRSAPLSLVQRRLWVAEQLSGGTSAYGMPMALRLCGELSVERLMSSFADVVRRHDVLRTAYRQNEEGDPVALIADEVRLDFPVIDLSGLSPSARQEQVAQATLENARTPIDLEQAPLLRGRILHLGPTEHVLLYAMHHIISDGWSMGLLINELVQVYEASLKGEPMPLAPLEIQYHDFALWQQALEEQGVLARQADYWKHRLSGYEGRLNLPLARPRGQTASYDGDALQFQLPTGLTGALRRLSSEAGVTLYSTLLASFQVLLHRLCAAQDLVVGADVAGREQPELERLIGFFVNVLPLRSRLDADATFASFLAQTQDNLLSALEHQDLPFDQIVEASGVPRHKGMNPLLQVLFVMNNVPVRTRSIKGLSVELLPALETHSKFDMALFVDEEEGQLRGTWQFATTLFGHEHIQHLIQAWTALLEQIVADQDIQLGAISMPVDNLAAAAKPATVPGPKADKLGKFLKRSVTPLAKPRPARVRESLVAAPQRFPLMLEPGEPQLDVIEWIHQNRPLIEQKLAEHAGILFRGFELDGIQGFEAFAEAIQPGLYGQYGDLPKKEGGKNTYRSTPYPERKMILFHNESSHQDRWPRKQMFYCEQAAPVGGATPVVDCRLMYEKLPSDLREKFEDKGLLYVRTFTDKLDVSWQHFFKTEDRREVEARCRAGGIQWRWLDNDELQTRTPGPAIITHPITGEKSFFNQVQLHHIYWLEPDVREDLLSMFGLERMPRHVYYGDGSPIEDEVMARIGDLYEACAVRFDWRKGDVILLDNMLVAHARDPFEGPRKIVVAMGDMYERSALEGQVDAGAAIQGIRNLEETGA
>NZ_CP054128.1|WP_173406728.1|2220072_2232423_+|non-ribosomal-peptide-synthase/polyketide-synthase
MNAEDALKLARRFIGLPLDKRRMFLAALDKEGVEFSGFPIPQGVEAEDRQALSYAQQRMWFLWQLEPGSAAYNLPGAVRLKGALSLKALEQAFASLVARHETLRTVFQRQADDSLLQVPTCAPLLIEQQDFSALPVAERERAVAEAAQQQSLLPFDLAVGPLLRVKLLKLDEQEHVLLLTLHHIVSDGWSMNVLIDEFIRCYDAHEAGQSPQLAPLPIQYSDYALWQRRWLEAGEQARQLEYWQAQLGSEHPVLELPTDHSRPAIPSYRGSRHEFAIDAALAEQLRSTAQQHGITLFMLLLGAFNVLLHRYSGQSDIRVGVPIANRNRDEIEGLIGFFVNTQVLRTELDGQTRVADLLRAVKETALGAQAHQDLPFERLVEALKLERSLSHTPLFQVMYNHQPHVVDLTTVSTASGLELGMLDWQGRTTQFDLTLDTYEKAGKLHAALTYANDLFETPTIARMARHWLRLLAAMVTDPSQRIGELPLLDADEHNTLVHGGNATAQRYPTDRCMHQLIEAQVARTPDAPALLFGEQSLSYAQLDARANRLAHLLRERGVRPDTLVGICVERSVEMVVGLLAIHKAGGAYVPLDPEYPQDRLAYMIEDSGIALLLTQRSLAAELPTDGVSVILLDQPSGWLDGYSERRPEVTVDPLSLAYVIYTSGSTGRPKGAGNSHAALVNRVCWMQQAYGLDDSDAVLQKTPFSFDVSVWEFFWPLMAGACLVVAAPGAHRDPLQLIDIINRYRISTLHFVPSMLQAFIHEPGVQTCEGLRRIVCSGEALPLDAQKQVFAKLPNASLYNLYGPTEAAIDVTHWTCVDEGADCVPIGRPIANLRTHVLDAQLAPVPYGVPGELYLGGAGLARSYHQRPALTAERFVPCPFHDGARLYRTGDRVRQRADGVIEYLGRLDHQVKLRGLRIELGEIETRLMQHPLVREAVVLVQDGKHLVGYLVLENTHPHEQWQQDLKAWLLGSLPEYMVPTYLMPLARLPVTANGKLDRKALPQPDAAPQQAFVAPQDALQIALAEIWQDVLGLERVGLEDNFFELGGDSIISIQVVSRARQVGIGINPRDLFQYQTVRSLALVASLDHHSAVDQGPITGEALLGPIQQQFFSRPMNAREHWNQSLLLTAREPLNGQWLDAALTCVINHHDALRLRFVPGADGWRQSHGPLLQSADLWLRDAQSAEQLNALCDEAQRSLSLQEGPLLRAMLVNLADGSQRLALVIHHLVVDGVSWRVLLEDLQQAYEQLAAGGGVTLPAKTSAFQSWTARLNAEAPRFDDQLAYWKAQHQGALDLPCDRPQGSLENAHGAKIEWRLDAELTRQLLQRAPAAYRTQVNDLLLTALARTITRWSGQPDTLIELEGHGREALFDDIDLTRTVGWFTSLFAVKLTASDDLGGSIKAIKEHLRGVPDKGLGYGVLRHLAAPSVRAELADLAPPRITFNYLGQFDRQFDEAALFVPSSEGSGVAQDPTAPLTNWLTVEGQVYGGELAMSWGFSREMFDRATVQQLVDRYAIELKALIEHCANLVTPQATPSDFPMAPVTQAQLDGLPVPAGQLDDLYPLSPMQQGLLFHTLYEQAAGEYVNQLRVDVQGLDTERFRAAWQATVDAQDILRSGFVWQGQLQQPLQIVHKKVPLPFTVLDWREHSDPSQALAALADSERAQGFDLSQAPLLRLVLVQTGAGQWHLIYTYHHILMDGWSNSQLLGEVMQRYSGRTSASAVGRYRDYIAWLQRQDGQLSEAFWSAQLATLQEPTRLASVMSASEIHSGHGDHFQTLDVPHTQALEQFARQQKVTLNTLVQAAWLLLLQRYTGHDCVAFGATVAGRPADLPGIEQQVGLFINTLPVIAAPRPDQSVGAWLQAVQAQNLSLRDFEHTPLADIQRWAGQGGEALFDNILVFENYPIAQALQEGAGQGVVFGEVTHQEQTHYPLSVAVTIGQNLALHYSFDRAHFSPAAIAGISEHLLQLLERFAESALRNLGEIALAGAEEQARQQAANHPQPYPTDIAVHQRIAHLAALNPHSTAVIFNGQRFSYGDIERRANQLAHALMAHGVGPETRVGVALPRSEGVIVALLAVLKAGGAYVPLDTGYPRERLAYLIEDSGLALLLTDSRVSAQLPLEGAAQVLELDRLDLSLQPLSAPSVQIDPQNLAYVIYTSGSTGNPKGVSVAHGPLAMHCQAIGERYEMHSSDCEFHFMSFAFDGAHERWLTSLTHGASLLIRDDSLWTPEQTYNALREHAVTVVAFPPVYLQQLAEHAEREGNPPKVRIYCFGGDAVANASFERVKRALNPDFIINGYGPTETVVTPLIWKAGRDEVCGAAYAPIGSRIGDRSAYVLDADLNLLPQGMAGELYLGGSGLARGYLNRPGLTAERFIADPFSAGGGLLYRTGDLVRQRADGTFDYLDRIDNQVKIRGFRIELGEVEASLQALEGVREAVVVAQEGSAGSGKRLVAYVVADESMAPRADFTEHLRDQLKATLPAHMVPAYLLLLERLPLTPNGKLDRKNLPKPDVSQLQQRYVAPRSTLEQQLASIWQDVLKLGQVGLRDNFFELGGDSIVSIQVVSRARQAGIHFTPKDLFQHQTIEALAVVARSGETTHVIDQGPVSGTLTLLPVQRLFFGQAIPERQHWNQAVMLKPTHALDARVLAPALSALVVHHDGLRLSFSERSEGWQASYRSPASHCAELLWAVDVPDAQALENIANRAQRSLDLQDGPLLRAVLATLADGSQRLLLVIHHLVVDGVSWRILFDDLQSAYRQLADGGMLQLPAKTTSAQVWAERLQGYARSASLQEELAYWQTRLEGVDGRLPMDNPQGGQHNHLALTVRTRLDASLTRQLLQDAPKAYRTQVNDLLLTALARVMVRWTGTDSALIQLEGHGREALFDEVDLTRTVGWFTSLYPARLTPSTDLGTSLKQIKEQLRSIPNKGLGFGALAHLADNPTQAILARLPVPQLTFNYLGQFDASFSEAQGALFVPASEGAGDELNAQAPLSNVLALNGQVFGGELNLGWTFSREQFNEATVQALADDYARELQGLIEHCCHGEHGGVTPSDFPLARLNQQQLDDLPVATAQIADLYPLSPMQQGMLFHSVYGDATGDYINQLRLDVEGLEPQRFRQAWQAAVDAHDILRTRFVWQGDLPDPVQIVSKQLDLPYRLHDLRDDVQPDETLQALAEAERRQLDLSAPALLRLLIVRLDEQRYQLIYTHHHILMDGWSNSQLLGEVLQRYSGQSVSVHGSRYRDYIAWLQRQDGAASEAFWKPALQRLEAPTRLADAIAQSGEADTGYGDHVQVLDETLTRRLEAFARASKVTINTLVQAAWLLLLQRYTGKDTVAFGATVAGRPADLPGIEQQIGLFINTLPVIASPRAEQSLDSWLQALQAQNLALREFEHTALLDIQRWAGQGGEALFDSLLVFENYPIAQALEQGAPDGLRFGPALTQEQTSYPLTLLVGLDRQLSVHMSYQRASFSAATVERLATHLAQLLGQMTDGGERCLSELSMLEFDEHQRLTHDWNPVDAPFEQALCIHQMIARQAEATPDALAVTFANTRLSYSEVDGRANRLAHKLIEMGVGPEVRVGVAMPRSEHLLIALLAVLKAGGAYVPLDPDYPAERVAYMLDDSRAKVLLTEQAVVATLSVPAETAVLMLDQLDLAHYPLSAPHTTVTPDNLAYVIYTSGSTGQPKGVAIAHRNVLALIDWSRSVYSRDDIQGVLASTSVCFDLSVWELFVTLANGGSLIIARNALELPQLPARDQVRLINSVPSAIAALQRSGEIPASVRIINLAGEPLKQSLVDSLYCESGIEHVYDLYGPSEDTTYSTWTRRTAGGTANIGRPVKHTASYLLDANLQAVPQGVSAELYLSGAGITRGYLGRAAMTAEKYVPNPFSTTGERLYRTGDLSRYRADGVLEYQGRIDHQVKIRGFRIELGEIEARLLQQPQVREVAVLAQDVSGGQQLVAYVVAPSLNLDDTEEQRALRDELKARLKDYLPDYMIPTHLLFLEQLPLTPNGKLDRKALPAVDTGWLQAGYVAPVTELEQQVAAIWAQVLTVQRVGLNDHFFELGGHSLLAVNVVSRMALELGLTLTPQLIFQHPVLRDFVAQLDTGDAPINEQKLSKLQALLDEMEEV
>NZ_CP054128.1|WP_047230459.1|2219074_2219809_+|thioesterase
MTQLTLLCLPYSGASAMVYSRWRRKVPQWLQVQPVELPGRGARFGEPLHTDMGPLAMQLARELRPTLQAPYALFGHSLGALLACEIAHALRELGCPEPVALFASGTAAPTMRADYDRGFATPKTDTELIEQLRTLNGTSEEVLANEELMALTLPVLRADFLLCGRFQPRTRAPLKCPVHVLGGTTDKASTEQLIGWSRETSGSFSVDMLAGGHFFIHEHEARVLRLIKDQLSVHHRRHGLAISA
>NZ_CP054128.1|WP_160891252.1|2263008_2264625_+|PvdJ/PvdD/PvdP-like-protein
MTISRRWFMAGLALTGAAVPAVYYGHRELTRPDPTITPGEASFDVADVAGQRRADTLRGIWTIRFSGSDAGLDGLPGDGLQVFLDIAHKGRGLVGCLDTAERLRADDEPRYRVLGDLAGDDKKQLSWRLIGTRQDAPVYEFIMTLDEVWAGFGNAGTATLSGRVLRLDRPLALPELDNQFIARKLPFPEARERTPLSPPLLAWLVSPEHRLFHQLWHASRDKWHSLDEDKRNALRGIGWQPGPRDHERDARGKRKDRNGSGVDFFFMHRHMLGTARSFQPLPSWPRFPLPQPELERDRLGFARYFDNHDGTALPPTWLASGDEQYAQWVSDIKTAETYHSNFQVWESRYRDPRYLSKLTLGQFGSEVELGLHDWLHMRWASVPRDPSNGHPVPFARDPADFAQRWYEPENDFLGDPFSSHVNPVFWAFHGWIDDRLEDWFRAHERFHPGEVSRLEVNGVPWFAPGRWVEIADPWLGPVTHGCSTTPGLQPGRSVEMDPETMKLALRITFGSDDKKLSELFRRVPQRPWYARNLKSKPV
>NZ_CP054128.1|WP_173406735.1|2265227_2266622_-|efflux-transporter-outer-membrane-subunit
MKAHLTLLAAGLLLAACGTPAPTPDSGIQPPPAWQSFDTATARTDNQQWWTHFGSPQLNRLIEQARRESYDLAAAMARVRQAEASAVIAGAPLLPAVTAGLNGTRQELLRGKGYSQLDVNRDNRTIDYYDAHLSASYELDFWGGKRAARNSALSSLSASQFDRATVELTLLSGVANSYTQALSLREQQRIAEQNLDNAQRVLDLVQTRYDAGSATALELSQQKSLVAAQQRRLPQVQQQAREALISLAALLGQPVQSVTLDDENFDRLHWPAIDAGVPSDLLSRRPDIAAAEARLAAAQADISVARAAMLPSVTLGLSLATGADIAEQLLRNNVYNLTAGLAAPIFNNGRLSAERDRATARQEELLELYRASIINGFADVEKALNGIHGLDQQRQWQSEELHQAQSAFDIAQSRYQAGAEDLLTVLETQRTLYAAQDMNVQLRLARVQASVALYRALGGGWRVM
>NZ_CP054128.1|WP_173406736.1|2266632_2268603_-|MacB-family-efflux-pump-subunit
MDAPLIELRDIRKVYGGGDSPRVEVLRGIDLSIHAGEFLAIVGASGSGKSTLMNILGCLDRPTSGDYWFAGEDVAGLGSDELAWLRREAFGFVFQGYHLIPSGTAQENVEMPAIYAGTSAAERHARASALLERLGLASRTGNRPHQLSGGQQQRVSIARALMNGGHIILADEPTGALDSQSGIEVMALLDELASQGHVVILITHDREVAARAKRIIEIRDGLIISDSAGALPHNVQANPKALQAVDLRQRLSAGSEHNGAWKGELLDAVQAAWRVMWINRFRTALTLLGIVIGVASVVVMLAVGEGSKRQVMAQMGAFGSNIIYLNGTAPTPRAAKGIISEHDLAALAALPEVQRIMPVNGADASVRFGNLDHTSYVGGNDTNFPTIFNWPVAQGSYFTDADERSAAAVAVIGHKVRHKLLKEVDDPIGRYILIENVPFQVVGVLAEKGASSGDSDADNRIAVPYSAASVRLFGSRHPEYVVIAARDAGKVREAEQAISRALLRLHDGKQDFELTNNAAMIQAEARTQGTLSLMLGAIAAISLLVGGIGVMNIMLMTVRERTREIGIRMATGARQRDILRQFLTEAVMLSVVGGLAGIGLALLVGGALLLGKIAVAFEWLAVFGAFGCALVTGVVFGFMPARKAARLDPVAALTSE
>NZ_CP054128.1|WP_076383897.1|2268603_2269755_-|efflux-RND-transporter-periplasmic-adaptor-subunit
MKRPRPTRRAWLLTFALLPAVAFAAWQAVAPSRESLITAPVTRGDIENSVTALGTLQPRRYVDVGAQASGQIRKIHVEAGDEVREGQLLVEIDPSTQKAKLDAGRFSIENLKAQLQEQRAQHDLAQQKFRRQQQLKAGGATREEDVQTAQAEVRATQARIDMFQAQIRQAQANLRSDEAELGYTRIFAPMSGTVVAVGAREGQTLNAQQQTPLILRIARLSPMTVWAEVSEADIGHVKPGMTAYFTTLAGGARRWSSTVRQILPVPPRPLEASQGGSLTGGRSGSERVVLYTVLLDVDNADRALMTEMTAQVFFVAAQARDVLTVPSAALQANARQVQVVADNGDVQPRTVRTGVSDRLRTEILDGLSEGDRVLIGPAVGSGG
>NZ_CP054128.1|WP_173406737.1|2270222_2270705_+|sigma-70-family-RNA-polymerase-sigma-factor
MLENYYRELVCFLNARLGNRQAAEDVVHDAYVRVLERASDTPIEQPRAFLYRTALNLVIDGHRRNTLRQVESLEVLDSEERFFTPSPHTSLDHGQRLDMLQRALAELPPLCRESFLLRKLEGLSHPQIAERLGISRALVEKHIVNAMKHCRTRMRQWDAH
>NZ_CP054128.1|WP_173406738.1|2270850_2272185_+|SidA/IucD/PvdA-family-monooxygenase
MTQAIASPNVHDLIGIGFGPSNLALAIALQERGPVQGELDVLFLDKQADYRWHGNTLVSQSELQISFLKDLVTLRNPTSPYSFVNYLKHHGRLVDFINLGTFYPCRMEYNDYLRWVAGQFTRQSRYGEEVLRIEPVLHNQQVEALRVISRDSQGEELVRSARSVVVSAGGTPRIPDAFTAFKEDARVFHHSQYLERMATQPCVNGQPMTIAIIGGGQSAAEAFIDLNDSFPSVQVDMILRGSALKPADDSPFVNEVFSPEFTDLVFQQPHSERERLVNEYHNTNYSVVDIDLIERIYGIFYRQKVSGIARHAFRTLTTVEKATASDAGVELAVRNNATGELSVRRYDAVVLATGYERQMHRTLLAPLEQYLGNFEVDRNYKLITDERCKAAIYMQGFCQASHGLSDTLLSILPVRADEIAGSLYEHSNHRGQSRSVRDLKLATA
>NZ_CP054128.1|WP_173406739.1|2272382_2275667_+|transporter-substrate-binding-domain-containing-protein
MTLFLRTGLVALLLGLSSVTPQVGAAPESLQVLGRSSVSDYSVSLGAADWNWLRGKGTLLLGASAPDYAPFGITSNGRDYEGLTADYAQLLGQMLHVDVRVQRYASREASLQALRSGEIDMLGTANGFEASDPALAMSQAYADDLPTLVARVADSQDLPTDLAGMRVAMLYHYLPTETVKAFYPDAALQLYPSTLSAIGAVAFGQADVYLGDSISSNYLISKNYLNNVQLADFSRMEVQPFAFAVSRENARLLRIINAALQAIPASERMSILRRWSAGGASIPGQQPLHFSVKEQRWLNAHPRITVAVNQNFPPLTFIDEQGHLRGISADVLARISLRTGLKFDIQRGNSLHDVIGRVRSGRADVLAAAPPSTELEGALRFTRPYLSNPFVLVAPLRGKVPLTLDQMEGKRLALIRGNVLREYLLEQFPRVHLVPAENAADAMSMVAAGTVDGAVNSLISARYMISRQYRGKLQITSTVGTFPESVALATHRDAPELHSILDKALLSISPEEMDELTNRWRSEVVIDDNYWLRNRTTIVQGFAIAALLLLLALGWVVYLRRLLEQLRVAKQSADDANRAKTTFLATMSHEIRTPMNAVIGMLELALKKADQGVMDRFAIEVASGAARGMLDLIGDILDIARIESGRLSLTPQRANLRELIESVARIFEGLAWQKQLHLQLELDAAINRDVLVDPLRFKQIVSNLLSNAIKFTDQGQVRLSVRAAPGDDAQCLPIRLRVEDTGCGISAEDQRRLFSPFTQASNNTQSARSGSGLGLVISRTLCEMMGGTLTLSSVPGEGTQIEVLLSLPALDALAQAPSAQVEALAPVRALNILVVDDYPANRLLLSQQLSYLGHRVREADDGVQGLRAWRAERFDVVITDCNMPLMSGYELARAIREAERTEGLSPGVILGFTANAQPEEKARCVEAGMDDCLFKPISLKELNSCLASVTQDCAAVPDERVPAPTTGDIDLSSLELLSAGDTGSIKKLLVEMVNSNAEDLAQLMRLLARQDLPGLADLAHRVKGGALMIRAQRLIAACEALESACRGGDRSLLAAAVDDVRQAMEHLTERLEAYVAGELAPAGARSGPRGSSHG
>NZ_CP054128.1|WP_047229284.1|2275795_2276230_+|chemotaxis-protein-CheY
MPNKALRIMIADTQHAHRMRLEHLFNQQGYFRIAPVSGLQELLTLVEYGSEPFDLVVVNAGLANGALNLHDFILDNPQLRHAMIYNTPQVGLSSAAVARRPGMHLSPAQLPDLASLASLMERIDPQASELTRPWLRPLRQGHAG
>NZ_CP054128.1|WP_172833789.1|2276306_2276960_+|response-regulator
MASAPFAFTWGVALKDVLIVDDHPVIRGALRLICQNEGFTGVRDASGVADARALIKEKAPDLVILDLVMNGFDGMDLLVWIMTQFPECGVLVFTSQDAQHFCNRCISAGARGFVTKKSDLKELIKAIHALKSGYSYFPQMPVRLDFQQRTEQQTLESLSTRELSILRMLAMGMRGKDIAEALFLSPKTVSTYKTRLLEKLGLKTLVGLSDFAKRNHL
>NZ_CP054128.1|WP_047229282.1|2277140_2278007_+|pirin-family-protein
MKNIIGVYTSPRAHWVGDGFPVRTLFSYDNLGKHISPFLLLDHAAPTQFEPTAERRGVGQHPHRGFETVTIVYQGELEHRDSTGSGGKIGPGDVQWMTAASGIIHEEFHSEDFARQGGFMEMVQLWVNLPAKDKMAPAGYQTILKSDIPSIDLKDNAGSLRLIAGRFEGHQGPAKTFTPIDVWDMRLNAGKNLTLDVHEGHNTALVVLRGTVQVNGRERVEAGQLALFDRAGEQLHLHANHDAVVLLLSGEPIDEPIVGHGPFVMNSEQEIHQAFNDFHSGRFGAMDD

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Crispr_ID: NZ_CP054128_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP054128_3

5503395-5503524

Orphan

Consensus_repeat	Method
CTGTCAGGCCGCCTCGCGAGCAGGCTTTGCTCCCACAGGTCCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP054128_3

>merge|NZ_CP054128|3|5503395-5503524|CRISPRCasFinder
CTGTCAGGCCGCCTCGCGAGCAGGCTTTGCTCCCACAGGTCCGGCTCAACATGTCTGATGGGTGTACACCCGCAAAAAACAGGCCGACTGTCAGGCCGCCTCGCGAGCAAGCTTTGCTCCCACAGGTCCG

>NZ_CP054128|3|3|5503395-5503524|CRISPRCasFinder
CTGTCAGGCCGCCTCGCGAGCAGGCTTTGCTCCCACAGGTCCG	GCTCAACATGTCTGATGGGTGTACACCCGCAAAAAACAGGCCGA
CTGTCAGGCCGCCTCGCGAGCAAGCTTTGCTCCCACAGGTCCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP054128.1\|WP_076386379.1\|5508648_5509128_-\|pilus-assembly-protein-PilX	unknown	unknown	gnl\|CDD\|227070
NZ_CP054128.1\|WP_047230173.1\|5510305_5510779_-\|GspH/FimT-family-protein	unknown	unknown	gnl\|CDD\|378793
NZ_CP054128.1\|WP_160893358.1\|5509137_5509851_-\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|227301
NZ_CP054128.1\|WP_076386371.1\|5500982_5502329_+\|sigma-54-dependent-Fis-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP054128.1\|WP_173407395.1\|5512461_5512905_-\|FKBP-type-peptidyl-prolyl-cis-trans-isomerase	unknown	unknown	gnl\|CDD\|223976
NZ_CP054128.1\|WP_047230174.1\|5509847_5510309_-\|type-IV-pilus-modification-protein-PilV	unknown	unknown	gnl\|CDD\|131575
NZ_CP054128.1\|WP_047229875.1\|5499170_5499404_+\|MYND-finger	unknown	unknown	gnl\|CDD\|181875
NZ_CP054128.1\|WP_047229874.1\|5498030_5499047_+\|outer-membrane-protein-assembly-factor-BamD	unknown	unknown	gnl\|CDD\|274513
NZ_CP054128.1\|WP_076386367.1\|5496194_5496920_-\|peptidoglycan-editing-factor-PgeF	unknown	unknown	gnl\|CDD\|182677
NZ_CP054128.1\|WP_047230171.1\|5511385_5512333_-\|4-hydroxy-3-methylbut-2-enyl-diphosphate-reductase	unknown	unknown	gnl\|CDD\|234893
NZ_CP054128.1\|WP_047229871.1\|5493499_5496064_-\|ATP-dependent-chaperone-ClpB	unknown	unknown	gnl\|CDD\|274529
NZ_CP054128.1\|WP_076386386.1\|5510893_5511409_+\|type-II-transport-protein-GspH	unknown	unknown	gnl\|CDD\|378793
NZ_CP054128.1\|WP_047229869.1\|5489545_5490844_+\|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|224172
NZ_CP054128.1\|WP_173407394.1\|5502379_5502745_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP054128.1\|WP_076386375.1\|5505148_5505550_-\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|227303
NZ_CP054128.1\|WP_047229870.1\|5491001_5492627_-\|methyl-accepting-chemotaxis-protein	unknown	unknown	gnl\|CDD\|223910
NZ_CP054128.1\|WP_047229873.1\|5496916_5497879_-\|23S-rRNA-pseudouridine(1911/1915/1917)-synthase-RluD	unknown	unknown	gnl\|CDD\|183020
NZ_CP054128.1\|WP_173407393.1\|5499393_5500986_+\|PAS-domain-containing-sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|236901
NZ_CP054128.1\|WP_160893360.1\|5505560_5508662_-\|pilus-assembly-protein	unknown	unknown	gnl\|CDD\|225953
NZ_CP054128.1\|WP_047230179.1\|5503992_5505093_-\|glycine-oxidase-ThiO	unknown	unknown	gnl\|CDD\|274092

Protein	Function_ID	Function_description	E-value
NZ_CP054128.1\|WP_076386379.1\|5508648_5509128_-\|pilus-assembly-protein-PilX	gnl\|CDD\|227070	COG4726, PilX, Tfp pilus assembly protein PilX [Cell motility and secretion / Intracellular trafficking and secretion].	3.09131e-15
NZ_CP054128.1\|WP_047230173.1\|5510305_5510779_-\|GspH/FimT-family-protein	gnl\|CDD\|378793	pfam12019, GspH, Type II transport protein GspH. GspH is involved in bacterial type II export systems. Like all pilins, GspH has an N-terminus alpha helix. This helix is followed by nine beta strands forming two beta sheets, one of five antiparallel strands and one of four antiparallel strands. GspH is a minor pseudopilin; it is expressed much less than other pseudopilins in the type II secretion pilus (major pilins). The function and localization of minor pseudo-pilins are still to be fully unraveled. It has been suggested that some minor pseudopilins may assemble either into the base or the tip of pili, or both. They function as initiators or regulators of pilus biogenesis and dynamics, and/or as adaptors between various pseudopilin component and other members of the T2SS.	1.45836e-06
NZ_CP054128.1\|WP_160893358.1\|5509137_5509851_-\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	gnl\|CDD\|227301	COG4966, PilW, Tfp pilus assembly protein PilW [Cell motility and secretion / Intracellular trafficking and secretion].	3.8959e-16
NZ_CP054128.1\|WP_076386371.1\|5500982_5502329_+\|sigma-54-dependent-Fis-family-transcriptional-regulator	gnl\|CDD\|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	0
NZ_CP054128.1\|WP_173407395.1\|5512461_5512905_-\|FKBP-type-peptidyl-prolyl-cis-trans-isomerase	gnl\|CDD\|223976	COG1047, SlpA, FKBP-type peptidyl-prolyl cis-trans isomerases 2 [Posttranslational modification, protein turnover, chaperones].	4.46467e-51
NZ_CP054128.1\|WP_047230174.1\|5509847_5510309_-\|type-IV-pilus-modification-protein-PilV	gnl\|CDD\|131575	TIGR02523, probable_type-4_fimbrial_biogenesis_protein, type IV pilus modification protein PilV. Pilus systems categorized as type IV pilins differ greatly from one another, with some showing greater similarty to type II or type III secretion systems than to each other. Members of this protein family represent the PilV protein of type IV pilus systems as found in Pseudomonas aeruginosa PAO1, Pseudomonas syringae DC3000, Neisseria meningitidis MC58, Xylella fastidiosa 9a5c, etc. [Cell envelope, Surface structures, Protein fate, Protein modification and repair].	1.00207e-24
NZ_CP054128.1\|WP_076386375.1\|5505148_5505550_-\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	gnl\|CDD\|227303	COG4968, PilE, Tfp pilus assembly protein PilE [Cell motility and secretion / Intracellular trafficking and secretion].	1.11251e-28
NZ_CP054128.1\|WP_047229874.1\|5498030_5499047_+\|outer-membrane-protein-assembly-factor-BamD	gnl\|CDD\|274513	TIGR03302, OM_YfiO, outer membrane assembly lipoprotein YfiO. Members of this protein family include YfiO, a near-essential protein of the outer membrane, part of a complex involved in protein insertion into the bacterial outer membrane. Many proteins in this family are annotated as ComL, based on the involvement of this protein in natural transformation with exogenous DNA in Neisseria gonorrhoeae. This protein family shows sequence similarity to, but is distinct from, the tol-pal system protein YbgF (TIGR02795). [Protein fate, Protein and peptide secretion and trafficking].	1.84918e-97
NZ_CP054128.1\|WP_076386367.1\|5496194_5496920_-\|peptidoglycan-editing-factor-PgeF	gnl\|CDD\|182677	PRK10723, PRK10723, polyphenol oxidase.	5.79393e-122
NZ_CP054128.1\|WP_047230171.1\|5511385_5512333_-\|4-hydroxy-3-methylbut-2-enyl-diphosphate-reductase	gnl\|CDD\|234893	PRK01045, ispH, 4-hydroxy-3-methylbut-2-enyl diphosphate reductase; Reviewed.	0
NZ_CP054128.1\|WP_047229871.1\|5493499_5496064_-\|ATP-dependent-chaperone-ClpB	gnl\|CDD\|274529	TIGR03346, chaperone_ClpB, ATP-dependent chaperone ClpB. Members of this protein family are the bacterial ATP-dependent chaperone ClpB. This protein belongs to the AAA family, ATPases associated with various cellular activities (pfam00004). This molecular chaperone does not act as a protease, but rather serves to disaggregate misfolded and aggregated proteins. [Protein fate, Protein folding and stabilization].	0
NZ_CP054128.1\|WP_076386386.1\|5510893_5511409_+\|type-II-transport-protein-GspH	gnl\|CDD\|378793	pfam12019, GspH, Type II transport protein GspH. GspH is involved in bacterial type II export systems. Like all pilins, GspH has an N-terminus alpha helix. This helix is followed by nine beta strands forming two beta sheets, one of five antiparallel strands and one of four antiparallel strands. GspH is a minor pseudopilin; it is expressed much less than other pseudopilins in the type II secretion pilus (major pilins). The function and localization of minor pseudo-pilins are still to be fully unraveled. It has been suggested that some minor pseudopilins may assemble either into the base or the tip of pili, or both. They function as initiators or regulators of pilus biogenesis and dynamics, and/or as adaptors between various pseudopilin component and other members of the T2SS.	4.33443e-15
NZ_CP054128.1\|WP_047229869.1\|5489545_5490844_+\|NAD(P)/FAD-dependent-oxidoreductase	gnl\|CDD\|224172	COG1252, Ndh, NADH dehydrogenase, FAD-containing subunit [Energy production and conversion].	5.19159e-148
NZ_CP054128.1\|WP_047229875.1\|5499170_5499404_+\|MYND-finger	gnl\|CDD\|181875	PRK09459, pspG, envelope stress response protein PspG.	0.000798907
NZ_CP054128.1\|WP_047229870.1\|5491001_5492627_-\|methyl-accepting-chemotaxis-protein	gnl\|CDD\|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	4.9202e-70
NZ_CP054128.1\|WP_047229873.1\|5496916_5497879_-\|23S-rRNA-pseudouridine(1911/1915/1917)-synthase-RluD	gnl\|CDD\|183020	PRK11180, rluD, 23S rRNA pseudouridine(1911/1915/1917) synthase RluD.	1.20335e-168
NZ_CP054128.1\|WP_173407393.1\|5499393_5500986_+\|PAS-domain-containing-sensor-histidine-kinase	gnl\|CDD\|236901	PRK11360, PRK11360, two-component system sensor histidine kinase AtoS.	2.68141e-40
NZ_CP054128.1\|WP_160893360.1\|5505560_5508662_-\|pilus-assembly-protein	gnl\|CDD\|225953	COG3419, PilY1, Tfp pilus assembly protein, tip-associated adhesin PilY1 [Cell motility and secretion / Intracellular trafficking and secretion].	8.42486e-79
NZ_CP054128.1\|WP_047230179.1\|5503992_5505093_-\|glycine-oxidase-ThiO	gnl\|CDD\|274092	TIGR02352, Glycine_oxidase, glycine oxidase ThiO. This family consists of the homotetrameric, FAD-dependent glycine oxidase ThiO, from species such as Bacillus subtilis that use glycine in thiamine biosynthesis. In general, members of this family will not be found in species such as E. coli that instead use tyrosine and the ThiH protein. [Biosynthesis of cofactors, prosthetic groups, and carriers, Thiamine].	6.58472e-75

>NZ_CP054128.1|WP_173407394.1|5502379_5502745_-|hypothetical-protein
MCDKSPSASETNNESPYSSLNPKQLDEAAKRALDYYLGPKPEAKKKPASNHLFTVVDGIDTECLLANLSETLASANATVSDLAFELEGSRRHVALGVQQLIELSELLANRVLDERVPVAEG
>NZ_CP054128.1|WP_076386371.1|5500982_5502329_+|sigma-54-dependent-Fis-family-transcriptional-regulator
MTTRSRQRILIVDDEPDIRELLDITLGRMKLDTRSAENLAQARALLAEDTFDLCLTDMRLPDGTGLELVQHIQQRYPQLPVAMITAYGSLETAIDALKAGAFDFLTKPVDLGRLRELVTSALRLPSVAIPAASIERCLLGDSPPMHNVRKQIEKLARSQAPVYISGESGCGKELVARLIHEQGPRSAQRFVPVNCGAIPTELMESEFFGHRKGSFSGAIEDKPGLFQAAHGGTLFLDEVADLPLAMQVKLLRAIQEKAVRAVGGQQEEVVDVRILCATHKDLDAEVTAGRFRQDLYYRLNVIELRVPPLRERREDIESLANHTLQRLAANTGSPAVKLHPQALDALRNYRFPGNVRELENMLERAYTLCEHQLIEAHDLRLAEGISTTDAGSPDLMRVDNLEDYLEDVERKLILQALEETRWNRTAAAQRLKLSFRSMRYRLKKLGLD
>NZ_CP054128.1|WP_173407393.1|5499393_5500986_+|PAS-domain-containing-sensor-histidine-kinase
MTAEQASSPRVKQAQRLLRLYHLYRLSIGITLVLLISSNMDNRLLEFANDDLLRSGSWLYLVLNILLVVFLENTRRPARLFGLALTDVLLLSWLFYAAGGAPSAIGNLLIVSVAIGNTLLRGRIGLLIAAVATLGIVGSSFFLDLSDSSRPSSYLQAGTLGALCFAAALLVQGLTRRLEASEILAEQRASEVVGLEALNALILQRMRTGILVLDGQRRVQLANESALSLLGMHDLVGQRLDDCSGALVERLQLWLNNPSLRPQSLTINGTGLTLQPSFIALGHHDQHQILVFLEDLAQVAQHAQQLKLASLGRLTAGIAHEIRNPLGAISHAAQLLRESEELNSADRRLTQIIQDHSQRMNRVIENVLQLSRRQQTTPQRLDLRIWLDQFVRQARENAAEHQHLHLSIDPGDYLTLMDPDQLTQVLDNLLRNAWRHSAMAHEEAEVWLKLFIAPHSQLSTLDIIDNGPGVTPDQQAHLFEPFFTTSSQGTGLGLYLSRELCESNQARLDFKPRQGGGCFRITFAHGRKQI
>NZ_CP054128.1|WP_047229875.1|5499170_5499404_+|MYND-finger
MLRLLFWIALIAAAIWLWRKFKGTSAAPNSPREQDAPPMVRCAHCGVHLPRDRALALEQQWYCSQAHLEQGPGTRDR
>NZ_CP054128.1|WP_047229874.1|5498030_5499047_+|outer-membrane-protein-assembly-factor-BamD
MQVKHLLLIAILALTAACSSKEVVDENLSEVELYQQAQTDLDNNSYTSATAKLKALESRYPFGRYADQAQLELIYANYKNAEPEAAKSAAERFIRLHPQHPNVDYAYYLKGLTSFDQDVGLLARFLPLDMTKRDPGAARDSYNEFAQLTSRFPNSRYSPDAKQRMIYLRNLLAAYEIHVADYYLTRQAYVAAANRGRYVVENFQETPSVGDGLAVMTEAYQRLHLDDLAATSLETLKLNYPDHPSLEDGQFTPRVDEADNRSWLSKATLGLIESRPPLPPGETRANQDVQRQFQDAKEAIPNELKPKDENGDVLEEEEPESESSDRSWFSYMTFGLFD
>NZ_CP054128.1|WP_047229873.1|5496916_5497879_-|23S-rRNA-pseudouridine(1911/1915/1917)-synthase-RluD
MSDKIELRAEVPSELGGQRLDQVAAQLFAEHSRSRLSAWIKDGRLTVDGAVIRPRDIVHGGAILELTAEQEAQGEWVAQDIALDIVYEDDDILVINKPAGLVVHPAAGHADGTLLNALLHHVPDIVNVPRAGIVHRLDKDTTGLMVVAKTIQAQTQLVTQLQSRSVSRIYECIVIGVVTAGGKINAPIGRHGQQRQRMAVMEGGKQAVSHYRVLERFRSHTHVRVKLETGRTHQIRVHMAHINFPLVGDPAYGGRFRIPPAASITMVESLKNFPRQALHARFLELDHPTTGKRMSWESPLPDDFVWLLTLLKQDREAFIG
>NZ_CP054128.1|WP_076386367.1|5496194_5496920_-|peptidoglycan-editing-factor-PgeF
MNDWLIPDWPAPAWVKACVTTRTGGVSLAPFDSLNLGDHVGDEPTAVAENRRRLTDRFAIRPAWLQQVHGITVVEADPAQVAIADASWTATPGIACTAMTADCLPVLFCNRAGTRVAAAHAGWRGLANGVLEATLDSLQVPADEILAWLGPAIGPQAFEVGPEVREAFMAQLPRAADAFVPGDTAGKFLADIYALARQRLAVRGVTAVYGGGQCTVTDPRFFSYRRNSRTGRFASLIWLDR
>NZ_CP054128.1|WP_047229871.1|5493499_5496064_-|ATP-dependent-chaperone-ClpB
MRIDRLTSKLQLALSDAQSLAVGLDHPGIEPAHLMQAMLEQQGGSIKPLLMQVGFDVSSLRKELAKELDQLPKIQNPTGDVNMSQDLARLLNQADRLAQQKGDQFISSELVLLAAMDENSKLGKLLLGQGVSKKALENAINNLRGGEAVNDANHEESRQALDKYTVDLTKRAEEGKLDPVIGRDDEIRRTIQVLQRRTKNNPVLIGEPGVGKTAIAEGLAQRIINGEVPDGLKGKRLLSLDMGSLIAGAKYRGEFEERLKALLNELSKQEGQIILFIDELHTMVGAGKGEGSMDAGNMLKPALARGELHCVGATTLNEYRQYIEKDAALERRFQKVLVEEPSEEDTIAILRGLKERYEVHHKVAITDGAIIAAAKLSHRYITDRQLPDKAIDLIDEAASRIRMEIDSKPEVLDRLERRLIQLKVESQALKKESDEAAKKRLERLQEEIVRHEREYSDLEEIWNSEKAEVQGSAQIQQKIEQSRQELEAARRKGDLNRMAELQYGVIPDLERSLQMVDQHGKSENQLLRSKVTEEEIAEVVSKWTGIPVSKMLEGERDKLLKMESLLHQRVIGQEEAVVAVSNAVRRSRAGLSDPNRPSGSFMFLGPTGVGKTELCKALAEFLFDTEEAMVRIDMSEFMEKHSVARLIGAPPGYVGYEEGGYLTEAVRRKPYSVILLDEVEKAHPDVFNILLQVLEDGRLTDSHGRTVDFRNTVIVMTSNLGSAQIQELVGDREAQRAAVMDAISTHFRPEFINRVDEVVIFEPLARDQIAGITEIQLGRLRSRLTERELKLQLSDEALDKLIAVGYDPVYGARPLKRAIQRWIENPLAQLILSGRFMPGETVTGTVENDEIVFN
>NZ_CP054128.1|WP_047229870.1|5491001_5492627_-|methyl-accepting-chemotaxis-protein
MVLRQLNIAPRAALGFALIAVLVALLGVFALGQMSSIRDSEVAVETQWLPSIRGGDEIRELMLRIRTISLRMALDQDPKNIPVYRGQMDTRDKELSEKIVSYEKLVITPEGKALYDQFKQTFAAYRTGIAQSFALAEQGRRDELIKLLLVDMKTVVDGSGKQLNDLAELFSRQVSIESQKSQEHYVNSRMIVSLFIVLAALATVALAMLLTRSIVKPLGEALNAAENVARGDLTRPIKTHGSDEVSRLLKALATMQQNLRETLQGISGSATQLATAADELNAVTVDSTHSLQQQNNEIEQAATAVTEMTTAVEEVARNAVSTSDATRQSSESASLGQQRVSDTVDAIGALASDVQVTGGLVQSLANQSQDIGKVLDVIRAIAEQTNLLALNAAIEAARAGESGRGFAVVADEVRALAYRTQQSTQEIEQMVQGMRSGATQALDSMQASSSRAASTLAMAERAGEALQTITASVNEIHERNLVIASAAEEQAQVAREVDRNLVNIRDLSVRSATGADQTSASSHELSQLANSLRTMVQRFQV
>NZ_CP054128.1|WP_047229869.1|5489545_5490844_+|NAD(P)/FAD-dependent-oxidoreductase
MTHRIVIVGGGAGGLELATRLGKTLGKRGTASVMLVDANLTHIWKPLLHEVAAGSLNSSEDELNYVAQAKWNHFGFQLGRMSGLDRERKSIQLAATYDEAGLELLPARELGYDTLVIAVGSTTNDFGTEGAAQHCLFLDTRKQAERFHQQLLNHYLRAHAGQTDVVERISVAIVGAGATGVELAAELHNAAHELAAYGLDRIKPENMHITLIEAGPRVLPALPERIGGPVHKTLEKLGVNVMTNAAVGQVTADSLITVDGKVIDASLKVWAAGIRAPDFLKEIDGLETNRINQLQVLPTLQTTRDENIFAFGDCAACPQPGSDRNVPPRAQAAHQQASLLAKSLKLRIEGKALPEYKYTDYGSLISLSRFSAVGNLMGNLTGSVMLEGWLARMFYVSLYRMHQMALYGMFRTAMLMLGSKIGRGTEPRLKLH
>NZ_CP054128.1|WP_047230179.1|5503992_5505093_-|glycine-oxidase-ThiO
MTRQQQVVIVGGGVIGLLTAFNLASEGQRVVLLDRSSVGQESSWAGGGIVSPLYPWRYSPAVTALAHWSQDFYPQLAQRLFAATGVDPQVHVTGLYWLDLDDQAEALAWAEREGRPLRAVEISAVHDAVPVLGAGFSRAIHMADVANVRNPRLVKSLKAALLALPNVTLHEQCEVGGFIRDGGRIVGVNSSEGPILGDQVVLAAGAWSGELLKTLGLKLPVEPVKGQMILYKCASDFLSSMVLAKGRYAIPRRDGHILVGSTLEREGFDKTPTDVALDSLKASAQQLIPALADAEVVGHWAGLRPGSPEGIPYIGEVPGFSGLWLNCGHYRNGLVLAPASCRLFVDVMLGREPVIDPAPYAPAGRL
>NZ_CP054128.1|WP_076386375.1|5505148_5505550_-|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein
MRRSNRGFTLIEIMIVIAIIGIVITVGYPSLTEYMKKGRRAEIAGLLSEQAQILERHYSKNNVYTNATGLSSGNDFYTITQTLMDQSFTLTAVRNSASSMATDKCGDFTINNTGARSIINAAAGLTAKDCWGR
>NZ_CP054128.1|WP_160893360.1|5505560_5508662_-|pilus-assembly-protein
MRNIKVRRDWKQALWGVLLSLYLAAPAYAFTPSDSPLLSAAAVTPNVMLLIDDSGSMNNIIWASGFDPTVTQTRTYACSASSNCNDRYELDLDDSNILLMSLLRGGCSSGWYGFYRPGLGRICLRLPDPVGGGDTRYTAKYLAYLVTLANGSNRDYTNGSIPRDYRINVARDVSNDLVANNRALRIGLATFNPPNFSNSGPGGYIARVVSDLSPVSGSVTQTQANANYSALINAINGLGAVANTPLAESYYEVTRYFRGMAPYHNNSPSTYTSPIQYRCQKNFGVVITDGLPTYDRTFPTNDPLGGSRLPNWDGISTNDGADRNGDAEGDTLYLDDIAKFAFDIDMRSTGTDVTGQSWNATDFPRQYLNTYTVGFAVTNTMLSDAARYGAGKYYPASDSEGLNSALSSALSDITSKAGSGGGGTTNGATLSTTSSYYQTTYDPKDWRGTIRAFGFTSAGTVDTAAVQWTTNTSIVPGATAPTYQSWNTATNTPVTLAYGNFSPAQQTSLSQGLPTGITGSDLVEWSKGVNKTGLKVRSALLGDIINSPLLLASPNDQTASDLLNDTSYSTYLATKAANMNANLVVNANDGFFSVINSANGTRRYAYMPSSVLPSLRDIADTNYINGVSHKFLVDGQIGVFDAQLGNAWKTVALGGTGAGGKAFYAVQLFDAAAGNALRALWEISAPTVANTANAFNDLGYAYARPEVARLADGRWAAFIANGYGSNTGVAALYVVDIRDGSLIRKITVNNSETGNGLSSVKLRVNSQNVVQAAYGGDLKGRMWKFDLSGTSPTAWGVAFAGQPLFTAPGGATQPITVQPLLAENPQGGTQVFFGTGKFNEAVDKLNKDLQGFYSIWDAVGGTGQIPVSSLQAQSITGVFSGSTGQFVTTSQTDVTYPAKNGWYLPLVYNNALTGERVINPASLVLGRVVFTTAAVDTTDPCASFGTGKLIEVDAFNGKMLNYAVLDTNGDGMLNSLDTVSSGVIFTGGIPTLSAVVSANGATNMIVNDSGGGITDLLGKSVGGSRRIMWRQIQ
>NZ_CP054128.1|WP_076386379.1|5508648_5509128_-|pilus-assembly-protein-PilX
MNSTPIKHRQRGMALLVSLVFLLLLTLIGLSSMQSATLQEKMTSSVMLRNQSFQLAEAALRVGESAVQAEAYSLPVCTTATQCAPPAESATLTTAGRNSSSGVTWIAVPGGFYGVQNLGTTLTAVNVPINTSATLYRITAVAVVGNNQRSVVESIYAKY
>NZ_CP054128.1|WP_160893358.1|5509137_5509851_-|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein
MNRHCRGFGLIELMIALVLSLIVVLGVVQIFIAAKNTYVSQGAAAVMQEDARFALSKMVQELRMVGMFGCLETVLDASSAGDFNASKVTPISWDNANLKLTLVTTDVGNSGGVPTWTVISDCRNTATAYTGARIPAAGQMAFPIRRLVYSFSNNQLLMGTGAGNPTQAVLVDNVRAFDVTFGVASSATDIAASSYSRNPSNPALIRSVRLTLTLFDPKNNVREQTFNVVAALRNRLL
>NZ_CP054128.1|WP_047230174.1|5509847_5510309_-|type-IV-pilus-modification-protein-PilV
MKGCSKQAQDGMTLIEVLVAVLILGVGLLGAAMVQLNALKYTDSSRMTSQASFIAYDMLDRIRANSGADYTVTPPSSPNLNVARDQDLYDFKTNIVSFGGATATGTVALHQRVYTITISWDDARAANTTNAAEARRSFVLTSRVAVDPPGATP
>NZ_CP054128.1|WP_047230173.1|5510305_5510779_-|GspH/FimT-family-protein
MDLRTKGFTLIEVLVALGVLLLLITLAVPALTGSVQGTKADTDIDDLRRALNFARMTAIDRGVTTRIRPTVQGSVWSSELTVYDSTGAEPNVLRVVPAMSSGATLTLTSDVTSIDFNNLGGLSAPATPVTFNYVRGAQSRTLSVCLNGRIVLGGSCG
>NZ_CP054128.1|WP_076386386.1|5510893_5511409_+|type-II-transport-protein-GspH
MYQQGFSLIELLMGLAIAAIVLPWAGSGYKALVESTDRDDAARLLASGLRSARSEAITRNRTVTIQGIDNDWSLGWQIMLDGDDQPLLTQHSRHARIIGNGPVKHSVRFASQGEPLLPSGAFQAGTLHVCAHHKPVSHHQVVLSRSGRVSLRSEKTEQALCEMDSKQGAHA
>NZ_CP054128.1|WP_047230171.1|5511385_5512333_-|4-hydroxy-3-methylbut-2-enyl-diphosphate-reductase
MQIKLANPRGFCAGVDRAIEIVNRALEVFGPPIYVRHEVVHNKFVVEDLRSRGAIFVEELDQVPDDVIVIFSAHGVSQAVRTEAAGRGLKVFDATCPLVTKVHIEVARYSRDGRECILIGHEGHPEVEGTMGQYDASNGGAIYLVEDEEDVAALQVRNPEKLAFVTQTTLSMDDTSRVIDALRARFPAIGGPRKDDICYATQNRQDAVKQLADECDVVLVVGSPNSSNSNRLRELAERMSTPAYLIDGAEDMQRSWFDGVERIGITAGASAPEVLVRGVIQQLQAWGATGADELSGREENVTFSMPKELRVRSLL
>NZ_CP054128.1|WP_173407395.1|5512461_5512905_-|FKBP-type-peptidyl-prolyl-cis-trans-isomerase
MTEQRIAQNTEVKLHFALHLENGDTVDSTFDKAPAVFKVGDGNLLPGFEAAIFGFKAGDKRTVVVPPENAFGQPNPQNVQTMPRSQFQDMELSEGLLVIFNDAANTELPGVVKAFDDAQVTVDFNHPLAGKTLNFEVEILDVKAVEI

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

337249 : 343294

uncultured_Caudovirales_phage(100.0%)

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_122612831.1\|337249_337963_-	arsenical resistance protein ArsH	A0A2H4J5V6	uncultured_Caudovirales_phage	3.5e-122	91.1
WP_122612830.1\|337992_338463_-	arsenate reductase ArsC	A0A2H4J8A6	uncultured_Caudovirales_phage	4.2e-68	82.1
WP_173406364.1\|338478_339762_-	arsenic transporter	A0A2H4J144	uncultured_Caudovirales_phage	9.1e-206	87.4
WP_122612828.1\|339789_340146_-	metalloregulator ArsR/SmtB family transcription factor	A0A2H4J145	uncultured_Caudovirales_phage	3.5e-46	78.8
WP_122612827.1\|340142_340565_-	arsenate reductase ArsC	A0A2H4J437	uncultured_Caudovirales_phage	9.4e-51	73.9
WP_173406365.1\|341922_342342_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_173406366.1\|342727_343294_+	N-acetyltransferase family protein	A0A2H4J136	uncultured_Caudovirales_phage	1.1e-59	62.6

DBSCAN-SWA_2

727133 : 788246

Diachasmimorpha_longicaudata_entomopoxvirus(18.18%)

transposase,holin

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_047230568.1\|727133_728159_-\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_047230429.1\|728280_730146_-	DEAD/DEAH box helicase	Q5GF26	Diachasmimorpha_longicaudata_entomopoxvirus	1.3e-43	30.4
WP_076383372.1\|730412_731189_-	transporter substrate-binding domain-containing protein	NA	NA	NA	NA
WP_047230427.1\|731244_732327_-	hypothetical protein	NA	NA	NA	NA
WP_047230426.1\|732410_733256_-	methylenetetrahydrofolate reductase [NAD(P)H]	NA	NA	NA	NA
WP_076383373.1\|733436_734846_-	adenosylhomocysteinase	S4W1G4	Pandoravirus	1.8e-37	31.1
WP_047230424.1\|735167_735572_+	acyl-CoA thioesterase	NA	NA	NA	NA
WP_047230423.1\|735775_736657_+	formate/nitrite transporter family protein	E7DYY8	Enterobacteria_phage	9.7e-74	53.2
WP_092401567.1\|736607_737777_-	MFS transporter	NA	NA	NA	NA
WP_173406463.1\|737973_738807_+	EamA family transporter	NA	NA	NA	NA
WP_047230420.1\|738858_739242_+	MAPEG family protein	A0A2H4J146	uncultured_Caudovirales_phage	2.3e-40	68.8
WP_076383375.1\|739395_740580_-	murein transglycosylase A	NA	NA	NA	NA
WP_047230418.1\|740703_741153_+	cytochrome c	NA	NA	NA	NA
WP_047230417.1\|741234_741630_-	DUF1090 domain-containing protein	NA	NA	NA	NA
WP_173406464.1\|741718_743392_-	NAD-dependent DNA ligase LigB	F8SJM3	Pseudomonas_phage	1.6e-29	26.4
WP_139048963.1\|743599_744220_+	LysE family transporter	NA	NA	NA	NA
WP_047230414.1\|744361_745552_-	methionine adenosyltransferase	A0A2H4PQS6	Staphylococcus_phage	1.1e-115	56.1
WP_047230413.1\|745571_746567_-	metalloregulator ArsR/SmtB family transcription factor	NA	NA	NA	NA
WP_047230412.1\|746824_748822_+	transketolase	NA	NA	NA	NA
WP_173406465.1\|748970_750026_+	erythrose-4-phosphate dehydrogenase	NA	NA	NA	NA
WP_139048965.1\|750050_751214_+	phosphoglycerate kinase	NA	NA	NA	NA
WP_047230409.1\|751245_751470_+	hypothetical protein	NA	NA	NA	NA
WP_047230408.1\|751527_751863_+	MliC family protein	NA	NA	NA	NA
WP_003177554.1\|752108_753173_+	fructose-bisphosphate aldolase class II	NA	NA	NA	NA
WP_047230501.1\|753575_753860_-	hypothetical protein	NA	NA	NA	NA
WP_139048969.1\|754323_754992_-	polysaccharide lyase family 7 protein	NA	NA	NA	NA
WP_173406466.1\|755297_755966_-	polysaccharide lyase family 7 protein	NA	NA	NA	NA
WP_076383385.1\|756245_756911_-	polysaccharide lyase family 7 protein	NA	NA	NA	NA
WP_076383386.1\|757231_759355_+	EAL domain-containing protein	G3MA91	Bacillus_virus	2.6e-24	39.3
WP_047230503.1\|759395_759899_+	M48 family metallopeptidase	NA	NA	NA	NA
WP_076383387.1\|759903_760200_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_047230495.1\|760253_760706_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_047230494.1\|760967_761705_+	transporter substrate-binding domain-containing protein	NA	NA	NA	NA
WP_160893959.1\|761847_764031_-	TIGR01666 family membrane protein	NA	NA	NA	NA
WP_047230492.1\|764274_765453_-	NAD(P)/FAD-dependent oxidoreductase	NA	NA	NA	NA
WP_047230502.1\|765596_766982_-	ATP-dependent RNA helicase DbpA	Q5GF26	Diachasmimorpha_longicaudata_entomopoxvirus	7.6e-49	30.9
WP_076383389.1\|767232_768660_-	multidrug transporter subunit MdtD	A0A0M3UL24	Mycobacterium_phage	2.8e-22	28.4
WP_173407508.1\|768853_770191_-	TldD/PmbA family protein	NA	NA	NA	NA
WP_173406467.1\|770205_771648_-	TldD/PmbA family protein	NA	NA	NA	NA
WP_076383391.1\|771879_773583_-\|holin	choline dehydrogenase	A0A1V0SI18	Klosneuvirus	6.5e-50	29.7
WP_173406468.1\|773802_775275_-	betaine-aldehyde dehydrogenase	NA	NA	NA	NA
WP_047230364.1\|775355_775976_-	transcriptional regulator BetI	NA	NA	NA	NA
WP_047230365.1\|776286_777465_-\|holin	choline ABC transporter ATP-binding protein	G3M9Y6	Bacillus_virus	4.5e-26	37.6
WP_047230366.1\|777461_778307_-\|holin	choline ABC transporter permease subunit	NA	NA	NA	NA
WP_047230367.1\|778373_779321_-\|holin	choline ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_173406469.1\|779743_781120_+	L-serine ammonia-lyase	NA	NA	NA	NA
WP_047230369.1\|781567_782671_+	GlxA family transcriptional regulator	NA	NA	NA	NA
WP_047230370.1\|782767_783031_-	hypothetical protein	NA	NA	NA	NA
WP_160893957.1\|783410_784574_-	gamma-butyrobetaine dioxygenase	NA	NA	NA	NA
WP_047230372.1\|784594_785071_-	thioesterase family protein	NA	NA	NA	NA
WP_047230373.1\|785233_786199_-	L-carnitine dehydrogenase	NA	NA	NA	NA
WP_076383396.1\|786341_787229_-	3-keto-5-aminohexanoate cleavage protein	NA	NA	NA	NA
WP_173406470.1\|787301_788246_-\|holin	choline ABC transporter substrate-binding protein	NA	NA	NA	NA

DBSCAN-SWA_3

3103907 : 3112720

Bacillus_phage(16.67%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_076384421.1\|3103907_3105338_-	transglycosylase SLT domain-containing protein	A0A223LD43	Bacillus_phage	5.4e-05	37.4
WP_173406901.1\|3105437_3106205_-	hydroxyacylglutathione hydrolase	NA	NA	NA	NA
WP_047225765.1\|3106270_3107029_+	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_047225766.1\|3107118_3107571_+	ribonuclease HI	J9Q745	Salmonella_phage	1.6e-40	56.3
WP_047225767.1\|3107730_3108492_+	DNA polymerase III subunit epsilon	A0A1X9SH08	Bradyrhizobium_phage	1.7e-37	38.6
WP_047225768.1\|3108764_3109379_+	GNAT family N-acetyltransferase	E4ZFP7	Streptococcus_phage	9.6e-20	39.6
WP_047225769.1\|3109344_3110238_-	LysR family transcriptional regulator	NA	NA	NA	NA
WP_047225770.1\|3110324_3110588_-	hypothetical protein	NA	NA	NA	NA
WP_047225771.1\|3110772_3111330_+	NAD(P)H-dependent oxidoreductase	A0A2P0ZL77	Lactobacillus_phage	1.4e-17	35.3
WP_107322357.1\|3111436_3112720_+	arsenic transporter	A0A2H4J144	uncultured_Caudovirales_phage	4.1e-182	78.2

DBSCAN-SWA_4

4049704 : 4055990

uncultured_Caudovirales_phage(83.33%)

tRNA

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_076386709.1\|4049704_4050097_+	sulfurtransferase complex subunit TusD	A0A2H4JA39	uncultured_Caudovirales_phage	1.2e-52	78.3
WP_076385465.1\|4050096_4050459_+	sulfurtransferase complex subunit TusC	A0A2H4J8C0	uncultured_Caudovirales_phage	1.4e-42	70.8
WP_076385467.1\|4050458_4050752_+	sulfurtransferase complex subunit TusB	A0A2H4JG28	uncultured_Caudovirales_phage	4.9e-30	65.7
WP_076385469.1\|4050748_4051084_+	TusE/DsrC/DsvC family sulfur relay protein	A0A2H4J8B6	uncultured_Caudovirales_phage	4.7e-45	80.2
WP_076385471.1\|4051080_4052082_+	glycosyl transferase family protein	A0A2H4JBY5	uncultured_Caudovirales_phage	3.8e-159	82.9
WP_076385473.1\|4052170_4053175_+	glutathione S-transferase family protein	NA	NA	NA	NA
WP_076385475.1\|4053314_4054709_-	uroporphyrinogen-III C-methyltransferase	NA	NA	NA	NA
WP_047227714.1\|4054709_4055990_-\|tRNA	serine--tRNA ligase	A0A1B1IVT2	uncultured_Mediterranean_phage	1.8e-97	53.6

DBSCAN-SWA_5

4483790 : 4491747

Enterobacteria_phage(42.86%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_173407192.1\|4483790_4484921_-	DegT/DnrJ/EryC1/StrS family aminotransferase	E5ES42	Bathycoccus_sp._RCC1105_virus	3.0e-43	30.3
WP_173407193.1\|4485539_4485947_-	WxcM-like domain-containing protein	NA	NA	NA	NA
WP_173407194.1\|4485943_4486510_-	dTDP-4-dehydrorhamnose 3,5-epimerase	I7HJC4	Enterobacteria_phage	1.1e-41	48.4
WP_173407195.1\|4486509_4487388_-	glucose-1-phosphate thymidylyltransferase RfbA	I7I009	Enterobacteria_phage	4.3e-114	70.0
WP_173407196.1\|4487377_4488283_-	dTDP-4-dehydrorhamnose reductase	A0A291LA50	Escherichia_phage	5.0e-25	33.3
WP_173407197.1\|4488279_4489422_-	dTDP-glucose 4,6-dehydratase	I7HTA3	Enterobacteria_phage	2.3e-99	53.1
WP_173407198.1\|4489411_4490422_-	NAD-dependent epimerase	A0A1V0SAI6	Catovirus	5.6e-33	31.7
WP_173407199.1\|4490418_4491747_-	UDP-glucose/GDP-mannose dehydrogenase family protein	A0A127AXI2	Bacillus_phage	3.6e-80	38.4

DBSCAN-SWA_6

5068990 : 5155137

Pseudomonas_phage(45.1%)

protease,tRNA,holin,lysis,tail,plate

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_047228431.1\|5068990_5070706_+\|tRNA	proline--tRNA ligase	A0A2K9L0T2	Tupanvirus	2.6e-06	28.6
WP_047228432.1\|5070723_5071677_+	hypothetical protein	NA	NA	NA	NA
WP_076386106.1\|5071854_5072916_-	DNA polymerase IV	NA	NA	NA	NA
WP_173407323.1\|5073758_5076401_+	bifunctional lysylphosphatidylglycerol flippase/synthetase MprF	NA	NA	NA	NA
WP_173407324.1\|5076400_5077684_+	virulence factor family protein	NA	NA	NA	NA
WP_076386113.1\|5077883_5079785_-	potassium transporter Kup	M1HZV6	Acanthocystis_turfacea_Chlorella_virus	8.5e-75	33.6
WP_047230036.1\|5080059_5081400_+	30S ribosomal protein S12 methylthiotransferase RimO	NA	NA	NA	NA
WP_173407325.1\|5081628_5082102_+	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_047230034.1\|5082175_5082886_+	RNA-binding protein S4	NA	NA	NA	NA
WP_047230033.1\|5082948_5083410_+	DUF1456 family protein	Q9EYF4	Enterobacteria_phage	3.2e-36	50.0
WP_047230032.1\|5083424_5084123_+\|tRNA	tRNA (N6-threonylcarbamoyladenosine(37)-N6)-methyltransferase TrmO	NA	NA	NA	NA
WP_003184787.1\|5084330_5085110_-	ferredoxin--NADP reductase	NA	NA	NA	NA
WP_047230031.1\|5085231_5086158_+	LysR family transcriptional regulator	NA	NA	NA	NA
WP_047230030.1\|5086169_5086532_-	diacylglycerol kinase	NA	NA	NA	NA
WP_047230029.1\|5086601_5087255_-	response regulator transcription factor	NA	NA	NA	NA
WP_047230028.1\|5087479_5088223_-	DTW domain-containing protein	NA	NA	NA	NA
WP_047230027.1\|5088404_5088827_+	quorum-sensing-regulated virulence factor family protein	NA	NA	NA	NA
WP_160891688.1\|5088827_5089022_-	hypothetical protein	NA	NA	NA	NA
WP_139051024.1\|5089473_5090592_+	TIGR00730 family Rossman fold protein	NA	NA	NA	NA
WP_107321595.1\|5090638_5091106_-	recombination regulator RecX	NA	NA	NA	NA
WP_047230023.1\|5091114_5092167_-	recombinase RecA	A0A0S2MVG1	Bacillus_phage	1.7e-109	61.8
WP_047230022.1\|5092250_5092751_-	CinA family protein	B5TK85	Pseudomonas_phage	1.6e-81	94.0
WP_047230021.1\|5092820_5093357_-\|lysis	lysis protein	B5TK84	Pseudomonas_phage	1.0e-73	84.3
WP_107323231.1\|5093338_5093902_-	glycoside hydrolase family 19 protein	B5TK83	Pseudomonas_phage	9.2e-94	88.8
WP_076386117.1\|5093927_5094374_-	hypothetical protein	B5TK82	Pseudomonas_phage	1.1e-36	56.6
WP_107321594.1\|5094374_5095271_-\|tail	phage tail protein	B5TK81	Pseudomonas_phage	6.6e-70	53.8
WP_107321593.1\|5095382_5095943_-\|tail	tail fiber assembly protein	B5TK80	Pseudomonas_phage	6.2e-74	67.7
WP_047230015.1\|5097074_5097584_-	hypothetical protein	B5TK78	Pseudomonas_phage	8.4e-78	92.3
WP_107321592.1\|5097580_5098744_-\|tail	phage tail protein	B5TK77	Pseudomonas_phage	7.7e-204	91.7
WP_047230013.1\|5098755_5099355_-	DUF2313 domain-containing protein	B5TK76	Pseudomonas_phage	4.7e-112	99.0
WP_047230012.1\|5099342_5100383_-\|plate	baseplate J/gp47 family protein	B5TK75	Pseudomonas_phage	8.2e-181	94.2
WP_047230011.1\|5100372_5100771_-	phage GP46 family protein	B5TK74	Pseudomonas_phage	3.5e-71	98.5
WP_173407326.1\|5100770_5101280_-\|plate	phage baseplate assembly protein	B5TK73	Pseudomonas_phage	2.1e-84	94.7
WP_173407327.1\|5101532_5102573_-\|plate	baseplate protein	B5TK72	Pseudomonas_phage	1.0e-191	97.4
WP_173407328.1\|5102576_5103815_-	DNA circularization N-terminal domain-containing protein	B5TK71	Pseudomonas_phage	4.5e-226	97.3
WP_107321589.1\|5103801_5105376_-\|tail	phage tail protein	B5TK70	Pseudomonas_phage	5.8e-154	93.7
WP_047230006.1\|5105506_5105803_-\|tail	phage tail assembly protein	B5TK69	Pseudomonas_phage	1.9e-45	99.0
WP_173407329.1\|5105799_5106147_-\|tail	phage tail tube protein	B5TK68	Pseudomonas_phage	9.7e-62	99.1
WP_047230005.1\|5106214_5107711_-\|tail	phage tail sheath subtilisin-like domain-containing protein	B5TK67	Pseudomonas_phage	4.1e-274	98.0
WP_047230004.1\|5107710_5107893_-	DUF2635 domain-containing protein	B5TK66	Pseudomonas_phage	6.9e-27	96.7
WP_047230003.1\|5107889_5108474_-	hypothetical protein	B5TK65	Pseudomonas_phage	6.2e-101	93.8
WP_173407330.1\|5108613_5109630_-	phage late control D family protein	A0A2H4JH05	uncultured_Caudovirales_phage	3.0e-103	55.8
WP_047230001.1\|5109639_5109852_-\|tail	tail protein X	A0A2H4JGD9	uncultured_Caudovirales_phage	5.8e-17	61.4
WP_047230000.1\|5109844_5110228_-\|tail	phage tail protein	A0A2H4JAC8	uncultured_Caudovirales_phage	2.1e-33	52.0
WP_173407331.1\|5110227_5112405_-\|tail	phage tail tape measure protein	NA	NA	NA	NA
WP_173407332.1\|5112533_5113109_-\|tail	phage tail assembly protein	B0ZSH0	Halomonas_phage	3.4e-27	39.0
WP_047229996.1\|5113288_5113795_-\|tail	phage major tail tube protein	Q6R4W3	Vibrio_virus	1.3e-22	34.5
WP_160891670.1\|5113794_5114961_-\|tail	phage tail protein	B0ZSG8	Halomonas_phage	2.3e-123	56.7
WP_173407333.1\|5114963_5115191_-	hypothetical protein	NA	NA	NA	NA
WP_160891668.1\|5115276_5115534_-	hypothetical protein	E3SP38	Cyanophage	7.8e-08	38.8
WP_160891666.1\|5115536_5116163_-	hypothetical protein	NA	NA	NA	NA
WP_173407334.1\|5116187_5116718_-	hypothetical protein	A2I2X8	Vibrio_virus	1.0e-49	61.9
WP_173407335.1\|5116714_5117359_-\|tail	phage tail protein I	A0A2H4JDK0	uncultured_Caudovirales_phage	7.4e-39	51.7
WP_173407336.1\|5117355_5118351_-\|plate	baseplate J/gp47 family protein	A0A2H4JC04	uncultured_Caudovirales_phage	9.2e-113	64.7
WP_076386161.1\|5118347_5118680_-\|plate	phage baseplate protein	A0A2H4JI46	uncultured_Caudovirales_phage	2.2e-39	72.7
WP_076386163.1\|5118691_5119303_-\|plate	phage baseplate assembly protein V	A0A2H4JBW8	uncultured_Caudovirales_phage	2.0e-46	56.0
WP_160891658.1\|5119306_5119819_-	hypothetical protein	A0A2H4JEV5	uncultured_Caudovirales_phage	1.7e-22	38.7
WP_047229987.1\|5119866_5120217_-\|holin	pyocin R2, holin	B5TK61	Pseudomonas_phage	1.7e-50	87.0
WP_047230040.1\|5120732_5121467_-	helix-turn-helix transcriptional regulator	B5TK58	Pseudomonas_phage	1.4e-134	97.1
WP_173407337.1\|5122114_5122474_+	hypothetical protein	B5TK57	Pseudomonas_phage	8.3e-48	85.7
WP_076386171.1\|5123211_5125791_+	DNA mismatch repair protein MutS	A0A1V0SJ67	Klosneuvirus	4.0e-27	22.1
WP_076386173.1\|5125933_5126257_+	ferredoxin family protein	NA	NA	NA	NA
WP_047227588.1\|5126752_5127760_-	RNA polymerase sigma factor RpoS	G8CLC7	Synechococcus_phage	6.6e-34	35.8
WP_047227587.1\|5127866_5128712_-	peptidoglycan DD-metalloendopeptidase family protein	A0A0S2SXL7	Bacillus_phage	1.9e-05	33.3
WP_171061419.1\|5128938_5129574_-	protein-L-isoaspartate(D-aspartate) O-methyltransferase	A0A1B1IU40	uncultured_Mediterranean_phage	1.2e-41	49.8
WP_047227585.1\|5129615_5130365_-	5'/3'-nucleotidase SurE	A0A1B1ITZ2	uncultured_Mediterranean_phage	8.0e-69	53.0
WP_047227584.1\|5130352_5131411_-\|tRNA	tRNA pseudouridine(13) synthase TruD	NA	NA	NA	NA
WP_076386175.1\|5131407_5131881_-	2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase	NA	NA	NA	NA
WP_076386177.1\|5131974_5132823_-	S-formylglutathione hydrolase	NA	NA	NA	NA
WP_025212132.1\|5132831_5133944_-	S-(hydroxymethyl)glutathione dehydrogenase/class III alcohol dehydrogenase	E3SJ82	Synechococcus_phage	1.2e-33	29.5
WP_047227581.1\|5134051_5134948_+	LysR family transcriptional regulator	NA	NA	NA	NA
WP_173407338.1\|5135083_5135791_-	2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase	NA	NA	NA	NA
WP_047227579.1\|5135787_5136066_-	cell division protein FtsB	NA	NA	NA	NA
WP_047227578.1\|5136236_5137526_-	phosphopyruvate hydratase	A0A1X9I5Z8	Streptococcus_phage	3.4e-136	59.2
WP_047227577.1\|5137685_5138531_-	3-deoxy-8-phosphooctulonate synthase	E3T537	Cafeteria_roenbergensis_virus	1.8e-48	42.4
WP_047227576.1\|5138535_5140167_-	CTP synthase	A0A1J0FA14	Only_Syngen_Nebraska_virus	1.0e-156	53.1
WP_173407339.1\|5140465_5141767_-\|tRNA	tRNA lysidine(34) synthetase TilS	NA	NA	NA	NA
WP_047227574.1\|5141898_5142846_-	acetyl-CoA carboxylase carboxyltransferase subunit alpha	NA	NA	NA	NA
WP_076386183.1\|5142997_5146519_-	DNA polymerase III subunit alpha	A0A1C9LWZ5	Streptomyces_phage	7.1e-200	36.7
WP_160891751.1\|5146615_5147260_-	ribonuclease HII	V5LS49	Emiliania_huxleyi_virus	5.9e-28	39.2
WP_173407340.1\|5147271_5148402_-	lipid-A-disaccharide synthase	NA	NA	NA	NA
WP_047227570.1\|5148404_5149181_-	acyl-ACP--UDP-N-acetylglucosamine O-acyltransferase	NA	NA	NA	NA
WP_047227569.1\|5149177_5149618_-	3-hydroxyacyl-ACP dehydratase FabZ	NA	NA	NA	NA
WP_047227568.1\|5149726_5150782_-	UDP-3-O-(3-hydroxymyristoyl)glucosamine N-acyltransferase	NA	NA	NA	NA
WP_047227567.1\|5150785_5151289_-	OmpH family outer membrane protein	NA	NA	NA	NA
WP_047227566.1\|5151334_5153710_-	outer membrane protein assembly factor BamA	NA	NA	NA	NA
WP_173407341.1\|5153784_5155137_-\|protease	RIP metalloprotease RseP	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_CP054128

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

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