CRISPRimmunity

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_CP022412	Bacteroides caccae strain ATCC 43185 chromosome, complete genome	3 crisprs	PrimPol,cas3,RT,PD-DExK,DEDDh,cas9	0	1	2	0

1. NZ_CP022412

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP022412_1

• CRISPR_ID: NZ_CP022412_1
• CRISPR_location: 1470871-1470976
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP022412_1

Consensus_repeat	Method
CAGTGTCTTTGACTACTGTATCATT	CRISPRCasFinder

spacers of NZ_CP022412_1

>1.1|1470896|56|NZ_CP022412|CRISPRCasFinder
GACAAAAGCGGTTGGTGCACTCAGTTCTGTTTTCACAGGTTCGTCTTTTTTAGTTA

CRISPR arrays and Neighbor proteins around NZ_CP022412_1

CRISPR arrays

The CRISPR arrays of NZ_CP022412_1

>merge|NZ_CP022412|1|1470871-1470976|CRISPRCasFinder
CAGTGTCTTTGACTACTGTATCATTGACAAAAGCGGTTGGTGCACTCAGTTCTGTTTTCACAGGTTCGTCTTTTTTAGTTACAGTGTCTTTGACTACTGTATCATT

>NZ_CP022412|1|1|1470871-1470976|CRISPRCasFinder
CAGTGTCTTTGACTACTGTATCATT	GACAAAAGCGGTTGGTGCACTCAGTTCTGTTTTCACAGGTTCGTCTTTTTTAGTTA
CAGTGTCTTTGACTACTGTATCATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022412.2|WP_005679063.1|1464771_1465926_+|lactaldehyde-reductase	unknown	unknown	gnl|CDD|182595
NZ_CP022412.2|WP_005679069.1|1467708_1468455_+|3-oxoacyl-[acyl-carrier-protein]-reductase	unknown	unknown	gnl|CDD|273824
NZ_CP022412.2|WP_005679059.1|1461570_1462827_+|L-rhamnose-isomerase	unknown	unknown	gnl|CDD|179217
NZ_CP022412.2|WP_005679078.1|1476833_1478066_+|insulinase-family-protein	unknown	unknown	gnl|CDD|223685
NZ_CP022412.2|WP_005679071.1|1469702_1470650_-|endonuclease/exonuclease/phosphatase-family-protein	unknown	unknown	gnl|CDD|197317
NZ_CP022412.2|WP_005679077.1|1475988_1476828_+|peptidylprolyl-isomerase	unknown	unknown	gnl|CDD|365914
NZ_CP022412.2|WP_005679084.1|1486407_1488750_+|BamA/TamA-family-outer-membrane-protein	unknown	unknown	gnl|CDD|227116
NZ_CP022412.2|WP_005679074.1|1472972_1474355_-|alpha-L-fucosidase	unknown	unknown	gnl|CDD|226195
NZ_CP022412.2|WP_005679073.1|1471371_1472928_-|sulfatase	unknown	unknown	gnl|CDD|293763
NZ_CP022412.2|WP_005679083.1|1481893_1486405_+|translocation/assembly-module-TamB-domain-containing-protein	unknown	unknown	gnl|CDD|367909
NZ_CP022412.2|WP_005679057.1|1459359_1459833_-|arginine-repressor	unknown	unknown	gnl|CDD|224355
NZ_CP022412.2|WP_005679076.1|1474527_1475898_-|sigma-54-dependent-Fis-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225114
NZ_CP022412.2|WP_005679085.1|1488875_1489787_+|hypothetical-protein	unknown	unknown	gnl|CDD|133024
NZ_CP022412.2|WP_005679060.1|1462830_1463850_+|L-rhamnose/proton-symporter-RhaT	unknown	unknown	gnl|CDD|237401
NZ_CP022412.2|WP_005679061.1|1463863_1464673_+|rhamnulose-1-phosphate-aldolase	unknown	unknown	gnl|CDD|179615
NZ_CP022412.2|WP_005679070.1|1468464_1469136_+|RNA-pseudouridine-synthase	unknown	unknown	gnl|CDD|211346
NZ_CP022412.2|WP_005679058.1|1460068_1461526_+|rhamnulokinase	unknown	unknown	gnl|CDD|198349
NZ_CP022412.2|WP_005679080.1|1479439_1481731_+|response-regulator	unknown	unknown	gnl|CDD|274362
NZ_CP022412.2|WP_005679068.1|1467101_1467692_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP022412.2|WP_005679079.1|1478062_1479421_+|MATE-family-efflux-transporter	unknown	unknown	gnl|CDD|240536

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP022412.2|WP_005679063.1|1464771_1465926_+|lactaldehyde-reductase	gnl|CDD|182595	PRK10624, PRK10624, L-1,2-propanediol oxidoreductase; Provisional.	0
NZ_CP022412.2|WP_005679069.1|1467708_1468455_+|3-oxoacyl-[acyl-carrier-protein]-reductase	gnl|CDD|273824	TIGR01830, 3-oxoacyl-_reductase_FabG, 3-oxoacyl-(acyl-carrier-protein) reductase. This model represents 3-oxoacyl-[ACP] reductase, also called 3-ketoacyl-acyl carrier protein reductase, an enzyme of fatty acid biosynthesis. [Fatty acid and phospholipid metabolism, Biosynthesis].	2.97021e-123
NZ_CP022412.2|WP_005679059.1|1461570_1462827_+|L-rhamnose-isomerase	gnl|CDD|179217	PRK01076, PRK01076, L-rhamnose isomerase; Provisional.	0
NZ_CP022412.2|WP_005679078.1|1476833_1478066_+|insulinase-family-protein	gnl|CDD|223685	COG0612, PqqL, Predicted Zn-dependent peptidases [General function prediction only].	3.84259e-70
NZ_CP022412.2|WP_005679071.1|1469702_1470650_-|endonuclease/exonuclease/phosphatase-family-protein	gnl|CDD|197317	cd09083, EEP-1, Exonuclease-Endonuclease-Phosphatase domain; uncharacterized family 1. This family of uncharacterized proteins belongs to a superfamily that includes the catalytic domain (exonuclease/endonuclease/phosphatase, EEP, domain) of a diverse set of proteins including the ExoIII family of apurinic/apyrimidinic (AP) endonucleases, inositol polyphosphate 5-phosphatases (INPP5), neutral sphingomyelinases (nSMases), deadenylases (such as the vertebrate circadian-clock regulated nocturnin), bacterial cytolethal distending toxin B (CdtB), deoxyribonuclease 1 (DNase1), the endonuclease domain of the non-LTR retrotransposon LINE-1, and related domains. These diverse enzymes share a common catalytic mechanism of cleaving phosphodiester bonds. Their substrates range from nucleic acids to phospholipids and perhaps, proteins.	8.83159e-117
NZ_CP022412.2|WP_005679077.1|1475988_1476828_+|peptidylprolyl-isomerase	gnl|CDD|365914	pfam00160, Pro_isomerase, Cyclophilin type peptidyl-prolyl cis-trans isomerase/CLD. The peptidyl-prolyl cis-trans isomerases, also known as cyclophilins, share this domain of about 109 amino acids. Cyclophilins have been found in all organisms studied so far and catalyze peptidyl-prolyl isomerisation during which the peptide bond preceding proline (the peptidyl-prolyl bond) is stabilized in the cis conformation. Mammalian cyclophilin A (CypA) is a major cellular target for the immunosuppressive drug cyclosporin A (CsA). Other roles for cyclophilins may include chaperone and cell signalling function.	2.06194e-36
NZ_CP022412.2|WP_005679084.1|1486407_1488750_+|BamA/TamA-family-outer-membrane-protein	gnl|CDD|227116	COG4775, COG4775, Outer membrane protein/protective antigen OMA87 [Cell envelope biogenesis, outer membrane].	3.95683e-21
NZ_CP022412.2|WP_005679074.1|1472972_1474355_-|alpha-L-fucosidase	gnl|CDD|226195	COG3669, COG3669, Alpha-L-fucosidase [Carbohydrate transport and metabolism].	2.52051e-24
NZ_CP022412.2|WP_005679073.1|1471371_1472928_-|sulfatase	gnl|CDD|293763	cd16144, ARS_like, uncharacterized arylsulfatase subfamily. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	2.14718e-176
NZ_CP022412.2|WP_005679083.1|1481893_1486405_+|translocation/assembly-module-TamB-domain-containing-protein	gnl|CDD|367909	pfam04357, TamB, TamB, inner membrane protein subunit of TAM complex. TamB is an integral inner membrane protein that forms a complex - the translocation and assembly module or TAM - with the outer membrane protein, TamA. TAM is responsible for the efficient secretion of the adhesin protein Ag43 in E.coli K-12.	4.39956e-24
NZ_CP022412.2|WP_005679057.1|1459359_1459833_-|arginine-repressor	gnl|CDD|224355	COG1438, ArgR, Arginine repressor [Transcription].	5.18832e-42
NZ_CP022412.2|WP_005679076.1|1474527_1475898_-|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].	5.07174e-173
NZ_CP022412.2|WP_005679085.1|1488875_1489787_+|hypothetical-protein	gnl|CDD|133024	cd04181, NTP_transferase, NTP_transferases catalyze the transfer of nucleotides onto phosphosugars. Nucleotidyltransferases transfer nucleotides onto phosphosugars. The enzyme family includes Alpha-D-Glucose-1-Phosphate Cytidylyltransferase, Mannose-1-phosphate guanyltransferase, and Glucose-1-phosphate thymidylyltransferase. The products are activated sugars that are precursors for synthesis of lipopolysaccharide, glycolipids and polysaccharides.	5.97554e-11
NZ_CP022412.2|WP_005679060.1|1462830_1463850_+|L-rhamnose/proton-symporter-RhaT	gnl|CDD|237401	PRK13499, PRK13499, L-rhamnose/proton symporter RhaT.	1.65604e-131
NZ_CP022412.2|WP_005679061.1|1463863_1464673_+|rhamnulose-1-phosphate-aldolase	gnl|CDD|179615	PRK03634, PRK03634, rhamnulose-1-phosphate aldolase; Provisional.	6.40539e-135
NZ_CP022412.2|WP_005679070.1|1468464_1469136_+|RNA-pseudouridine-synthase	gnl|CDD|211346	cd02869, PseudoU_synth_RluA_like, Pseudouridine synthase, RluA family. This group is comprised of eukaryotic, bacterial and archeal proteins similar to eight site specific Escherichia coli pseudouridine synthases: RsuA, RluA, RluB, RluC, RluD, RluE, RluF and TruA. Pseudouridine synthases catalyze the isomerization of specific uridines in a n RNA molecule to pseudouridines (5-ribosyluracil, psi) requiring no cofactors. E. coli RluC for example makes psi955, 2504 and 2580 in 23S RNA. Some psi sites such as psi1917 in 23S RNA made by RluD are universally conserved. Other psi sites occur in a more restricted fashion, for example psi2819 in 21S mitochondrial ribosomal RNA made by S. cerevisiae Pus5p is only found in mitochondrial large subunit rRNAs from some other species and in gram negative bacteria. The E. coli counterpart of this psi residue is psi2580 in 23S rRNA. psi2604in 23S RNA made by RluF has only been detected in E.coli.	3.03548e-57
NZ_CP022412.2|WP_005679058.1|1460068_1461526_+|rhamnulokinase	gnl|CDD|198349	cd07771, FGGY_RhuK, L-rhamnulose kinases; a subfamily of the FGGY family of carbohydrate kinases. This subfamily is predominantly composed of bacterial L-rhamnulose kinases (RhuK, also known as rhamnulokinase; EC 2.7.1.5), which are encoded by the rhaB gene and catalyze the ATP-dependent phosphorylation of L-rhamnulose to produce L-rhamnulose-1-phosphate and ADP. Some uncharacterized homologous sequences are also included in this subfamily. The prototypical member of this subfamily is Escherichia coli RhuK, which exists as a monomer composed of two large domains. The ATP binding site is located in the cleft between the two domains. This model includes both the N-terminal domain, which adopts a ribonuclease H-like fold, and the structurally related C-terminal domain. The presence of divalent Mg2+ or Mn2+ is required for catalysis. Although an intramolecular disulfide bridge is present in Rhuk, disulfide formation is not important to the regulation of RhuK enzymatic activity. Members of this subfamily belong to the FGGY family of carbohydrate kinases.	0
NZ_CP022412.2|WP_005679080.1|1479439_1481731_+|response-regulator	gnl|CDD|274362	TIGR02956, sensor_protein_TorS, TMAO reductase sytem sensor TorS. This protein, TorS, is part of a regulatory system for the torCAD operon that encodes the pterin molybdenum cofactor-containing enzyme trimethylamine-N-oxide (TMAO) reductase (TorA), a cognate chaperone (TorD), and a penta-haem cytochrome (TorC). TorS works together with the inducer-binding protein TorT and the response regulator TorR. TorS contains histidine kinase ATPase (pfam02518), HAMP (pfam00672), phosphoacceptor (pfam00512), and phosphotransfer (pfam01627) domains and a response regulator receiver domain (pfam00072). [Signal transduction, Two-component systems].	5.36005e-55
NZ_CP022412.2|WP_005679068.1|1467101_1467692_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	6.83845e-12
NZ_CP022412.2|WP_005679079.1|1478062_1479421_+|MATE-family-efflux-transporter	gnl|CDD|240536	cd13131, MATE_NorM_like, Subfamily of the multidrug and toxic compound extrusion (MATE)-like proteins similar to Vibrio cholerae NorM. The integral membrane proteins from the MATE family are involved in exporting metabolites across the cell membrane and are responsible for multidrug resistance (MDR) in many bacteria and animals. This subfamily includes Vibrio cholerae NorM and functions most likely as a multidrug efflux pump, removing xenobiotics from the interior of the cell. The pump utilizes a cation gradient across the membrane to facilitate the export process. NorM appears to bind monovalent cations in an outward-facing conformation and may subsequently cycle through an inward-facing and outward-facing conformation to capture and release its substrate.	1.21993e-107

Protein sequences

>NZ_CP022412.2|WP_005679071.1|1469702_1470650_-|endonuclease/exonuclease/phosphatase-family-protein
MKLRSLLLIALVAVVFCGCHSYQPTSITVASYNLRNANGSDSAKGNGWGQRYPVIAKMVQYHDFDIFGTQECFIHQLKDMKEALPGYDYIGVGRDDGKEKGEHSAIFYRTDKFDVIEKGDFWLSETPDVPSKGWDAVLPRICSWGHFKCKDTGFEFLFFNLHMDHIGKKARVESAYLVQDKMKELGKGKELPAILTGDFNVDQTHQSYDAFVSKGVLCDSYEKCDFRYATNGTFNDFDPDSFTESRIDHVFVSPVFKVKRYGVLTDTYRSIRGNGGKKDATDCPEEIDIKAYQARTPSDHFPVKVELVFEGEEQK
>NZ_CP022412.2|WP_005679070.1|1468464_1469136_+|RNA-pseudouridine-synthase
MTVVYEDNHIIVVNKTASEIVQADKTGDTPLSETVKQYLKEKYQKPGNVFLGVTHRLDRPVSGLVIFAKTSKALTRLNEMFRAGEVKKTYWAVVKNAPKESEGELVHFLVRNEKQNKSYAYDKEVPNSKKAVLDYRLIGRSENYYLLEVDLKTGRHHQIRCQLAKMGCPIKGDLKYGSPRSNPDGSICLHARRVRFVHPVSKELIELKAPLPEGNLWKGFELF
>NZ_CP022412.2|WP_005679069.1|1467708_1468455_+|3-oxoacyl-[acyl-carrier-protein]-reductase
MGLLDGKTAIVTGAARGIGKAIALKFAAEGANIAFTDLVIDENAENTTKELEAMGVKAKGYASNAANFEDTAKVVEEIHKDFGRIDILVNNAGITRDGLMMRMSEQQWDMVINVNLKSAFNFIHACTPVMMRQKAGSIINMASVVGVHGNAGQANYAASKAGMIALAKSIAQELGSRGIRANAIAPGFILTDMTAALSDEVRAEWAKKIPLRRGGTPEDVANIATFLASDMSSYVSGQVIQVDGGMNM
>NZ_CP022412.2|WP_005679068.1|1467101_1467692_+|TetR/AcrR-family-transcriptional-regulator
MTVSKTKAKLVDVARQLFAKMGVENTTMNDIALASKKGRRTLYTYFKSKDEIYLAVVESELDILSDMMKRVAEKNISPDEKLLEMIYTRLDAVKEVVYRNGTLRAYFFRDIWRVEKVRKKFDAKEVQLFKAVLLEGQAKGVFHIDDVEMTADLIHYCVKGIEVPYIRGHIGAHLDEDTRNKYVANIVFGALHRTEI
>NZ_CP022412.2|WP_005679063.1|1464771_1465926_+|lactaldehyde-reductase
MNRIILNETSYFGAGCRSVIAVEAARRGFKKAFFVTDKDLVKFGVAAEIIKVFDDNKIPYELYSDVKANPTIANVQNGVAAYKASGADFIVALGGGSSIDTAKGIGIVVNNPDFADVKSLEGVADTKHKAVPTFALPTTAGTAAEVTINYVIIDEDARKKMVCVDPNDIPAVAIVDPELMYSMPKGLTAATGMDALTHAIESYITPGAWAMSDMFELKAIEMIAQNLKAAVDNGKDVVAREAMSQAQYIAGMGFSNVGLGIVHSMAHPLGAFYDTPHGVANALLLPYVMEYNAESPAAPKYINIAKAMGVETAGMSEAEGVKAAIEAVKSLSLSIGIPQKLHEINVKEEDIPALAVAAFNDVCTGGNPRPTSVEDIEVLYRKAF
>NZ_CP022412.2|WP_005679061.1|1463863_1464673_+|rhamnulose-1-phosphate-aldolase
MKSILENRSALAKEVDKVAEVAGYLWQKGWAERNGGNITINITEFVDDEIRRMQPISEVRSIGVTLPYLKGCYFYCKGTNKRMRDLARWPMENGSVIRILDDCASYVIIADEAVVPTSELPSHLSVHNDLLSKNSPYKASVHTHPIELIAMTHCEKFLQKDVATNLLWSMIPETKAFCPRGLGIIPYKLPSSVELAEATIKELQDYDVVMWEKHGVFAVDCDAMQAFDQIDVLNKSALIYIAAKNMGFEPDGMSREQMKEMTVAFNLPK
>NZ_CP022412.2|WP_005679060.1|1462830_1463850_+|L-rhamnose/proton-symporter-RhaT
MDILIGLLIIAIGSFCQSSSYVPIKKVKEWSWESFWLIQGVFAWLVFPFLGSLLGVSEGGSLFELWGAGGAGMSILYGILWGVGGLTFGLSMRYLGVALGQSISLGTCAGFGTLLPALFAGTNLFEGNGLVLLLGVCITLAGIAIIGYAGSLRAQNMSEEEKRAAVKDFALTKGLLVALLAGVMSACFALGLDAGTPIKEAALAGGVEGLYAGLPVIFLVTFGGFLTNAIYCLQQNVTNKSMNDYAKGKVWSNNLVFCALAGVLWYMQFFGLEMGKSFLAESPVLLAFSWCILMALNVTFSNVWGIILKEWKGVSVKTITVLVCGLLVLIFSLVFPNLF
>NZ_CP022412.2|WP_005679059.1|1461570_1462827_+|L-rhamnose-isomerase
MKKEELIQKAYEIAVERYAAVGVDTEQVLKTMQDFHLSLHCWQADDVAGFEVQAGSLTGGIQATGNYPGKARNIDELRADILKAASYIPGTHRLNLHEIYGDFQRKVVDRDQVEPEHFKSWIEWGKEHNMKLDFNSTSFSHPKSGDLSLSNPDEGIRQFWIEHTKRCRAVAEEMGKAQGDPCIMNLWVHDGSKDITVNRMKYRALLKDSLDQIFATGYKNMKDCIESKVFGIGLESYTVGSNDFYIGYGASHNKMITLDTGHFHPTESVADKVSSLLLYVPELMLHVSRPVRWDSDHVTIMDDPTMELFSEIVRCGALDRVHYGLDYFDASINRIGAYVIGSRAAQKCMTRALLEPIAKLREYEANGQGFQRLALLEEEKALPWNAVWDMFCLKNNVPVGEDFIAEIEKYEAEVTSKR
>NZ_CP022412.2|WP_005679058.1|1460068_1461526_+|rhamnulokinase
MKQNFFAVDLGATSGRTILGTFIEGGLNLEEINRFPNHLIEVGGHFYWDIYALYRHVIEGLKLVAHRGESIASIGIDTWGVDFVCVGKDGNLLRQPYAYRDPHTVGAPDALFSRISRSKVYEKTGIQIMNFNSLFQLDTLRRNNDSALEAADKILFMPDALSYMLTGKMVMEYTIASTAQLVNAQTRSLEPELLKVVGLTEKNFGRFVFPGEKVGVLTEEVQKITGLGAVPVIAVIGHDTGAAVAAVPALDRNFAYLSSGTWSLMGVETDAPVINTETETLNFTNEGGVEGTIRLLKNICGMWLLERCRLNWGDTSYPELISEADACEPFRSLINPDDDCFVNPANMEKSIAAYCHATGQPVPEQRGQVVRCIFESLALRYRQVLENLRSLSPRPIETLHVIGGGSRNDLLNQFTANAIGIPVVAGPSEATAIGNVMIQAMAAGEATDMAGMRRLIQRSVPLKTYHPQDTDAWDTAYIHFKNCIR
>NZ_CP022412.2|WP_005679057.1|1459359_1459833_-|arginine-repressor
MKKKANRLDAIKMIISSKEVGSQEELLQELNREGFELTQATLSRDLKQLKVAKAASMNGKYVYVLPNNIMYKRSTDQSAGEMLRSNGFISLQFSGNIAVIRTRPGYASSMAYDIDNNEFSEILGTIAGDDTIMLVLREGVATSKIRQLLSLIIPNIE
>NZ_CP022412.2|WP_005679073.1|1471371_1472928_-|sulfatase
MNKKKLFPLALVPLAATSLQAQSNIQTGRTDKRPNIILFMVDDMGWQDTSLPFWTQKTHYNELYETPNMERLARQGMMFTQAYASSISSPTRCSLITGTNAARHRVTNWTLQKNTMTDRKNKQLAVPDWNYNGVSQVPGTNNTFVGTSFVQILKDNGYHTIHCGKAHFGSIDTPGEDPHHWGFEVNIAGHAAGGLASYLGEENYGHTKDGKPVSLMAVPGLEKYWGTETFVTEALTQEAIKALNKAKKYNQPFYLYMAQYAIHVPLNKDMRFYDKYKKKGMTDHEAAYATLIEGMDKSLGDLMNWLEKNDEADNTIIIFMSDNGGLAAESYWRDGKLHTQNHPLNSGKGSTYEGGIREPMIVSWPGVVKPGSKCDNYLLIEDFYPSILEMAGIKKYKTVQPIDGISFIPLLKQTGNPSKGRSLFWNMPNNWGNDGPGINFNCAVRNGDWKLIYYYGTGKKELFNIPNDIGESNDLSAQHPDIVKRLSKELGNYLRKVDAQRPTFKATGQPCPWPDEKK
>NZ_CP022412.2|WP_005679074.1|1472972_1474355_-|alpha-L-fucosidase
MKKFNFICLSILYSICSFAQQQSIPVPKPHQLKWHEAEMGAVFHYDLHVFDGIRYGQGNNRITPIEDYNIFNPTELNTDQWVQAAKAAGCKFAVLTATHETGFGLWQSDVNPYCLKAVKWKDGKGDIVRDFVNSCHKYGLQPGIYIGIRWNSLLGIHNFKAEGEGEFARNRQAWYKRLCENMVTELCTRYGDLYMIWFDGGADNPRRDGPNVEPIVNKYQPDCLFYHNVDRADFRWGGSETGTVEYPCWSTFPYPYSHSNATEPARNHNILLKHGDKDGKYWVPAMADTPLRGANGRHEWFWEPDDENNIYPLDALMDKYEKSVGRNATLILGLTPDPTGLIPIGDTQRLKEMGDEINRRFSSPIAKTLGKKKSLTLNLGKKQTVNYCIIQENIKNGERIRQYKIEAKVNGKWQPVCSGESVGHKRIEKFDPIEASALRLTIPESVALPDIINFSTYYIK
>NZ_CP022412.2|WP_005679076.1|1474527_1475898_-|sigma-54-dependent-Fis-family-transcriptional-regulator
MKAILIVEDDITFGMMLKTWLGKKGFEVSSVSNIARARKHIESQTVDLVLSDLRLPDYEGIDLLKWMNDRGLDIPLIIMTGYADIQSAVLAMKLGARDYIAKPVNPEELLKKISEALQTERTPTAHSAAKMSSKKVSPASSKETTETRRAYLEGESDAAKQLYNYVGLVAPTNMSVLINGSSGTGKEYVAHRIHQLSKRSDKPFIAVDCGSIPKELAASEFFGHVKGSFTGALTDKTGAFVAANGGTIFLDEIGNLSYEVQIQLLRALQERKIRPVGSTQEISVDIRLVSATNENLEQGIEKGTFREDLYHRINEFTLRMPDLKERKEDILLFANFFLDQANKELDKHLIGFDAKASQALLSYHWPGNLRQMKNIVKRATLLAQGSFITLLELGTDLLDTTTTCTTSMSLRNEETEKEHILEALRQTGNNKSKAAQLLNIDRKTLYNKLKLYNIDL
>NZ_CP022412.2|WP_005679077.1|1475988_1476828_+|peptidylprolyl-isomerase
MKKITLILLTISFCGLTACKTGTKKGGDMDKETLVKIETTAGDIKVKLYNETPKHRDNFIKLVKDGVYEGTLFHRVIKDFMIQAGDPDSKNAPKGKMLGAGDVGYTVPAEFVYPKYFHKKGALSAARQGDNVNPKKESSGCQFYIVTGKVYNDSTLLGMESQMNENKINVIFNKLAQKHMKEIYKMRKANDENGLYDLQEKLFAEAQELSAKEPEFHFTPEQIEAYTTVGGTPHLDGEYTVFGEVVEGMDVVDKIQKVKTDRSDRPEEDVKIIKATILD
>NZ_CP022412.2|WP_005679078.1|1476833_1478066_+|insulinase-family-protein
MKINRHILDNGLRLVHSRDESTQMVALNILYNVGARDEHPEHTGFAHLFEHLMFGGSVNIPDYDMPLQLAGGENNAWTNNDITNYYLTVPRQNVETGFWLESDRMLSLDFSERSLEVQRGVVMEEFKQRCLNQPYGDVGHLLRPLAYQKHPYQWPTIGKDLSHVANATLEEVKAFFFRFYAPNNAILAVTGNISFEEAVELTEKWFGSVPRREVPVRNLPQEPEQTEERRLTVERNVPLDSLFMAYHMCDHRHPDYYVFDILSDVLSNGRSSRLNQHLVQEKQLFSSIDAYISGSVDAGLFHIAGKPSAGVSLELAEAAVRDELDRLQQELVDGQELEKVKNKFESTQIFGNINYLNVATNLAWFELLGKAEDLEKEVERYRSVTAMQLREVAQSAFRKENGVVLYYKSK
>NZ_CP022412.2|WP_005679079.1|1478062_1479421_+|MATE-family-efflux-transporter
MRNIYRTYREHYKALFFLGLPIVIGQIGVIVLGFADTLMIGHHSTVELGAASFVNNVFNLAIIFSTGFSYGLTPVVGGLYGTHQFAPAGQALRNSLLANLMVALLLTLCMTVLYLNIENLGQPEELIPLIKPYYLVLLASLVFVMLFNGFKQFTDGITDTKTAMWILLGGNVLNIIGNYLLIYGKLGLPELGLLGAGISTLFSRIMMVLVFIIIFLRSSRFIRYKVGFFRLGWSRAIFGRLNGLGWPVAFQMGMETASFSLSAIMIGWLGTIALASHQVMLAISQFTFMMYYGMGAAVAVRVSNFKGQNDILNVRRSAYAGFHLMMTLGVVLSFIVFLCRNYLGGWFTDSPEVAAMVTSLIFPFLVYQFGDGLQITFANALRGISDVKLMMLIAFIAYFIISLPVGYFCGFVMGWGVVGVWMAFPFGLTSAGLMLWWRFHYMTKLPTPQVNT
>NZ_CP022412.2|WP_005679080.1|1479439_1481731_+|response-regulator
MASYRSTKLKVTIGYTLLLAILLFSLVFVHREMETLSAADDQENLRTDSLLTLLHEKDRNTIQMLRVLSEANDSLLSASEIEEIISEQDSVITQQRVQHRVITKRDSLLTTPKKKGFFKRLAEVFVPTKQDSAVLVNTSMEVATDTILEPTTSKDSLQQKIRMATEEKRLQRRKTIRRTSTKYQRMNSQLTARMDSLIKQYEEEMTLRARQDAEMQQEVRMRSARTIGGIAIGAVLLSVFFLILIVRDISRSNRYRRQLEEANKRAEDLLIAREKLMLAITHDFKAPLGSIMGYTELLSRLTEDERQRFYLDNMKSSSEHLLKLVSDLLDFHRLDLNKAEVNRVTFNPSQLFEEIHVSFEPLTAAKGLTLQCHVAQELNGRYISDPLRLRQIVNNLLSNAVKFTPKGEIALTAKYDSSKLTIAISDTGKGMATEDRERIFQEFTRLSGAQGEEGFGLGLSIVKKLVVLLEGTIDVQSKLGEGSCFTVILPLYPVGKSVSERALEEKTISAEDPVTLPPMKVIRVLLIDDDKIQLSLTAAMLKQHGIDAVCCEQLEELIEQLRTSVFDVLLTDIQMPAINGFDLVKLLRASNIPQAKTIPVIAVTARSEMDIDALQEHGFAGCLHKPFTVKELLLTVNEGQLAADEAHITEDMQTVSSLNFSALTAFSEDDADAAHSIIQTFIEETGKNADRMQQALAGKEVDGIAAMAHKLLPLFTLIGAMEAVPLLNWLETQRGQCFSEEIGEKTACVLLEIQKVLEEARKV
>NZ_CP022412.2|WP_005679083.1|1481893_1486405_+|translocation/assembly-module-TamB-domain-containing-protein
MKRKWIRRVSWILLTPVLLFVILMILLYIPPVQNLLRREVTAYASKATGMQIQVERIDLRFPLNLLVRGVEVIQQPDTLLSLESLNVRVQAWPLVKGKVEVDEVTLSQVAFNSANLIEGMKIKGVLGRFFLQSHGVDLSNELAVINQTELSDTHVQMLMNDTTTTPKDTTASAPVNWKVDLHKLKLKNVSFSMQLPADSMRMAAHIEEAFINDAQADLKNQFYELKQFLLSGSSANYDTGAAKPGEGFDASHIAVRDIRIGLDSLLYKGRDMNAVIREFSMNERSGLSITSLTGRAFSNDSIIRIPGIKLQTPHSEIDLSAQTYWELVNIPTTGRLSAGLNAYIGKEDVMLFAGGLPDSFKEAYPFRPLVVRAGTDGNLKQMQISRFTVDLPGAFSMKGGGILENLADSLTRSGTIGLDMITQNLNFLTALTGEAPNGTIVIPDSMNLKARVELKGPEYKANLHLKQGQGSMGVNAELNTSTEAYAADLKIDNLQLHNFLPKDSIYELSLSADAKGRGLDVMSYRALAKLNLSLDQLHYARYQLSNVHLTGALKGALVTANLTSDNALLKMTTDAEYNLAHRYPDGKVTVDVTQLDLHELGLMPQPMKRPLAFNLSAEARQNRVFTHLTSGDMKLNLSARSGVNSLISQSTHFMDVLMKQIDEKALNHAELREALPTAILSFSAGKENPLAYFLATKNISYHDVSMKFGTAPDWGINGKAAVHALKMDTLQLDTIFFTVKQDTTLMKLRAGVINGPKNPQFSFATTLTGEIRDRDAELLVDYKNGKGETGVLLGVNARPLFEGHGKGNGIAFTLIPENPIVAFQRFHFNENHNWIYLHKNMRVYANVDMWDEEGMGFRVHSVPGDTVSLQNIDVEIRRIRLQEITSVLPYFPEITGLFSLEAHYIQTEKDLQLSAEASVDELTYERQRIGDVALGATWLPGEQGKQYLNAYLNHEQAEVLVADGKLVPTRTGKDSLEVNTTLEHFPLRVANVFIPDQMVTLSGDMDGNLNITGSTEQPLINGELVLDSVAVLSRQYGARFMFDNRPVQIKNNRLEFDKFAIYTTSKNPFTIDGYVDFRDMSRPMANLNMLAQNYTLLDAKRTRESLVYGKVFADFRATVKGPLDGLNMRGNVSLLGNTDVSYVLTDSPLTVQDRLGSLVTFTSFSDTTTVVRQEVPTVSLGGLDMVMMVHIDPSVRVKVDLDASNDNRIELEGGGDLSMKYTPQGDLTLTGRYTLSGGLMKYALPVIAAKEFAIDNGSYVEWTGNPMDPMLNFKATDRIRASVSEGENGGSRMVNFDVSVVVKNRLDNLSFAFDVAAPEDATVQNELTAMGAEERGKQALYIMVMKTYLGTGPIGGGGGGLGKLNMGSALTSVLSSQINSLMGNLKNASLSVGVEDHDDSETGSKRTDYSFRYSQRLFNNRFQIVIGGKVSQGENATNDAESFIDNISLEYRLDRTGTRYIRLFYDKNYESVLEGEITETGVGIVLRKKLDKLSELFIFKKKK
>NZ_CP022412.2|WP_005679084.1|1486407_1488750_+|BamA/TamA-family-outer-membrane-protein
MKEIHINILAVCLISVVLLSACSVTKHLPEGEVLYTGSKTVILNKSTTPVGETALTEIDAALDKTPSTKMFGGILPIPFKMWMYNDFVKYKKGFGKWMFNRFAANPPVFISTVNPEVRVKVTTNLLRDYGYFNGKVAYETVVDKKDSLKAGIIYTVDMKNPYFIDTVYYQRFTPQTLRIMERGRRMSYISPGEQFNVVDLDEERSRISTLLRNLGYFYFRPDYMTYQADTTLVPGGHISLRLIPVPGLPAAAQRPYYVGDASVYLFGKNGEAPNDSMMYKNLNIHYYNKLQVRPNMLYRWLNYQQFVRNAQMRASNRTRLYSQYRQEQIQEKLSQLGIFSYMDIQYAPKDTTAVCDTLDITMQATFAKPLDAELELNVVTKSNDQTGPGASFGVTRNNVFGGGESWNVKLKGSYEWQTGGGEKSSLMNSWEMGISTSLTFPRVVFPRWGKREFDFPATTTFRLYIDQLNRARYYKLLSFGGNATYDFQPTRTSRHSITPFKLTFNVLQHQSKEFMEIAADNPALYVSLDNQFIPAMEYTYTYDNASVRRVKNPIWWQSTVTSAGNVTATIYRAFGKPYNEEGKKLLGAPFSQFMKFNTEFRHLWNMDKNNKIASRVALGALFAYGNATIAPYSEQFYVGGANSIRAFTVRSIGPGGYHPKDSKYSYLDQTGTFRFEANVEYRFRIFKSIWGATFLDAGNVWLLRKDEARPDSQLRLKTFPKQIALGTGVGVRYDMDILVFRLDFGIPLHLPYDTERSGYYNVTGTFFKNLGIHFAIGYPF
>NZ_CP022412.2|WP_005679085.1|1488875_1489787_+|hypothetical-protein
MKPTLFLLAAGMGSRYGGLKQLDGLGPNGETIMDYSIYDAINAGFGKLVFVIRKDFEQDFRDKIISKYEGHIPCELVFQALDALPEGFTCPADRTKPWGTNHAVMMGADVIKEPFAVINCDDFYGRDSFQVMGKFLSALPADSKNVYSMVGFRVGNTLSESGTVSRGICSTDDKGLLTSVVERTKIQRLDGEVKYIDDNGEWTATPDTTPVSMNFWGFTPDYFAYSQEFFKTFLSDPKNMENLKSEFFIPLMVDKLINDGTATVEVLDTASKWFGVTYPEDRQSVVDKIQALVDAGEYPAKLF

Crispr_ID: NZ_CP022412_2

• CRISPR_ID: NZ_CP022412_2
• CRISPR_location: 1550700-1550800
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP022412_2

Consensus_repeat	Method
CGTTTCAATAGTGGTGAAGGTGG	CRISPRCasFinder

spacers of NZ_CP022412_2

>2.1|1550723|55|NZ_CP022412|CRISPRCasFinder
CGACCGTCCTCAGCGTCCTTACAACCGCGAAGGTGGTGACCGCCCGTATCGTCCT

CRISPR arrays and Neighbor proteins around NZ_CP022412_2

CRISPR arrays

The CRISPR arrays of NZ_CP022412_2

>merge|NZ_CP022412|2|1550700-1550800|CRISPRCasFinder
CGTTTCAATAGTGGTGAAGGTGGCGACCGTCCTCAGCGTCCTTACAACCGCGAAGGTGGTGACCGCCCGTATCGTCCTCGCTTCAATAGTGGTGAAGGTGG

>NZ_CP022412|2|2|1550700-1550800|CRISPRCasFinder
CGTTTCAATAGTGGTGAAGGTGG	CGACCGTCCTCAGCGTCCTTACAACCGCGAAGGTGGTGACCGCCCGTATCGTCCT
CGCTTCAATAGTGGTGAAGGTGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022412.2|WP_032855465.1|1537383_1539372_-|family-20-glycosylhydrolase	unknown	unknown	gnl|CDD|119334
NZ_CP022412.2|WP_005679148.1|1551781_1553185_+|asparagine--tRNA-ligase	unknown	unknown	gnl|CDD|235176
NZ_CP022412.2|WP_004314716.1|1554107_1554569_+|50S-ribosomal-protein-L13	unknown	unknown	gnl|CDD|181703
NZ_CP022412.2|WP_005679155.1|1557634_1557985_-|translation-initiation-factor	unknown	unknown	gnl|CDD|211319
NZ_CP022412.2|WP_005679143.1|1543634_1546856_+|carbamoyl-phosphate-synthase-(glutamine-hydrolyzing)-large-subunit	unknown	unknown	gnl|CDD|273581
NZ_CP022412.2|WP_005679152.1|1555082_1555919_+|30S-ribosomal-protein-S2	unknown	unknown	gnl|CDD|235396
NZ_CP022412.2|WP_005679154.1|1557103_1557613_-|TlpA-family-protein-disulfide-reductase	unknown	unknown	gnl|CDD|239264
NZ_CP022412.2|WP_081447323.1|1543441_1543561_+|methyltransferase	unknown	unknown	unknown
NZ_CP022412.2|WP_005679138.1|1541213_1541684_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP022412.2|WP_005679156.1|1558150_1558801_+|redox-sensing-transcriptional-repressor-Rex	unknown	unknown	gnl|CDD|235486
NZ_CP022412.2|WP_005679153.1|1556040_1557033_+|elongation-factor-Ts	unknown	unknown	gnl|CDD|236491
NZ_CP022412.2|WP_005679157.1|1558801_1559416_+|fumarylacetoacetate-hydrolase-family-protein	unknown	unknown	gnl|CDD|223257
NZ_CP022412.2|WP_005679149.1|1553324_1553816_+|DUF4488-domain-containing-protein	unknown	unknown	gnl|CDD|381210
NZ_CP022412.2|WP_005679142.1|1542192_1543287_-|tryptophan--tRNA-ligase	unknown	unknown	gnl|CDD|183400
NZ_CP022412.2|WP_005679145.1|1547754_1548306_+|sugar-O-acetyltransferase	unknown	unknown	gnl|CDD|100047
NZ_CP022412.2|WP_005679144.1|1546975_1547749_+|peroxide-stress-protein-YaaA	unknown	unknown	gnl|CDD|377151
NZ_CP022412.2|WP_005679146.1|1548771_1550118_+|adenylosuccinate-lyase	unknown	unknown	gnl|CDD|236452
NZ_CP022412.2|WP_005679136.1|1539468_1540107_-|DsbA-family-protein	unknown	unknown	gnl|CDD|375718
NZ_CP022412.2|WP_005679151.1|1554575_1554962_+|30S-ribosomal-protein-S9	unknown	unknown	gnl|CDD|178888
NZ_CP022412.2|WP_005679137.1|1540484_1541186_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP022412.2|WP_032855465.1|1537383_1539372_-|family-20-glycosylhydrolase	gnl|CDD|119334	cd06564, GH20_DspB_LnbB-like, Glycosyl hydrolase family 20 (GH20) catalytic domain of dispersin B (DspB), lacto-N-biosidase (LnbB) and related proteins. Dispersin B is a soluble beta-N-acetylglucosamidase found in bacteria that hydrolyzes the beta-1,6-linkages of PGA (poly-beta-(1,6)-N-acetylglucosamine), a major component of the extracellular polysaccharide matrix. Lacto-N-biosidase hydrolyzes lacto-N-biose (LNB) type I oligosaccharides at the nonreducing terminus to produce lacto-N-biose as part of the GNB/LNB (galacto-N-biose/lacto-N-biose I) degradation pathway. The lacto-N-biosidase from Bifidobacterium bifidum has this GH20 domain, a carbohydrate binding module 32, and a bacterial immunoglobulin-like domain 2, as well as a YSIRK signal peptide and a G5 membrane anchor at the N and C termini, respectively. The GH20 hexosaminidases are thought to act via a catalytic mechanism in which the catalytic nucleophile is not provided by solvent or the enzyme, but by the substrate itself.	3.18138e-129
NZ_CP022412.2|WP_005679136.1|1539468_1540107_-|DsbA-family-protein	gnl|CDD|375718	pfam18291, HU-HIG, HU domain fused to wHTH, Ig, or Glycine-rich motif. Rapidly-diverging family of HU domains predominantly observed in the bacteroidetes lineage with a predicted role in recognition and possible interception of the DNA of parasitic elements, a counter-conflict strategy preventing incorporation of these elements into the host genome.	1.86129e-32
NZ_CP022412.2|WP_004314716.1|1554107_1554569_+|50S-ribosomal-protein-L13	gnl|CDD|181703	PRK09216, rplM, 50S ribosomal protein L13; Reviewed.	1.9096e-84
NZ_CP022412.2|WP_005679155.1|1557634_1557985_-|translation-initiation-factor	gnl|CDD|211319	cd11567, YciH_like, Homologs of eIF1/SUI1 including Escherichia coli YciH. Members of the eIF1/SUI1 (eukaryotic initiation factor 1) family are found in eukaryotes, archaea, and some bacteria; eukaryotic members are understood to play an important role in accurate initiator codon recognition during translation initiation. The function of non-eukaryotic family members is unclear. Escherichia coli YciH is a non-essential protein and was reported to be able to perform some of the functions of IF3 in prokaryotic initiation.	2.72762e-28
NZ_CP022412.2|WP_005679143.1|1543634_1546856_+|carbamoyl-phosphate-synthase-(glutamine-hydrolyzing)-large-subunit	gnl|CDD|273581	TIGR01369, Carbamoyl-phosphate_synthase_large_chain, carbamoyl-phosphate synthase, large subunit. Carbamoyl-phosphate synthase (CPSase) catalyzes the first committed step in pyrimidine, arginine, and urea biosynthesis. In general, it is a glutamine-dependent enzyme, EC 6.3.5.5, termed CPSase II in eukaryotes. An exception is the mammalian mitochondrial urea-cycle form, CPSase I, in which the glutamine amidotransferase domain active site Cys on the small subunit has been lost, and the enzyme is ammonia-dependent. In both CPSase I and the closely related, glutamine-dependent CPSase III (allosterically activated by acetyl-glutamate) demonstrated in some other vertebrates, the small and large chain regions are fused in a single polypeptide chain. This model represents the large chain of glutamine-hydrolysing carbamoyl-phosphate synthases, or the corresponding regions of larger, multifunctional proteins, as found in all domains of life, and CPSase I forms are considered exceptions within the family. In several thermophilic species (Methanobacterium thermoautotrophicum, Methanococcus jannaschii, Aquifex aeolicus), the large subunit appears split, at different points, into two separate genes. [Purines, pyrimidines, nucleosides, and nucleotides, Pyrimidine ribonucleotide biosynthesis].	0
NZ_CP022412.2|WP_005679152.1|1555082_1555919_+|30S-ribosomal-protein-S2	gnl|CDD|235396	PRK05299, rpsB, 30S ribosomal protein S2; Provisional.	5.4808e-134
NZ_CP022412.2|WP_005679154.1|1557103_1557613_-|TlpA-family-protein-disulfide-reductase	gnl|CDD|239264	cd02966, TlpA_like_family, TlpA-like family; composed of TlpA, ResA, DsbE and similar proteins. TlpA, ResA and DsbE are bacterial protein disulfide reductases with important roles in cytochrome maturation. They are membrane-anchored proteins with a soluble TRX domain containing a CXXC motif located in the periplasm. The TRX domains of this family contain an insert, approximately 25 residues in length, which correspond to an extra alpha helix and a beta strand when compared with TRX. TlpA catalyzes an essential reaction in the biogenesis of cytochrome aa3, while ResA and DsbE are essential proteins in cytochrome c maturation. Also included in this family are proteins containing a TlpA-like TRX domain with domain architectures similar to E. coli DipZ protein, and the N-terminal TRX domain of PilB protein from Neisseria which acts as a disulfide reductase that can recylce methionine sulfoxide reductases.	1.94923e-30
NZ_CP022412.2|WP_005679156.1|1558150_1558801_+|redox-sensing-transcriptional-repressor-Rex	gnl|CDD|235486	PRK05472, PRK05472, redox-sensing transcriptional repressor Rex; Provisional.	3.05828e-97
NZ_CP022412.2|WP_005679157.1|1558801_1559416_+|fumarylacetoacetate-hydrolase-family-protein	gnl|CDD|223257	COG0179, MhpD, 2-keto-4-pentenoate hydratase/2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) [Secondary metabolites biosynthesis, transport, and catabolism].	1.18421e-61
NZ_CP022412.2|WP_005679153.1|1556040_1557033_+|elongation-factor-Ts	gnl|CDD|236491	PRK09377, tsf, elongation factor Ts; Provisional.	4.23363e-96
NZ_CP022412.2|WP_005679149.1|1553324_1553816_+|DUF4488-domain-containing-protein	gnl|CDD|381210	cd19435, lipocalin_Bacteroides, bacteroides lipocalin. An uncharacterized Bacteroides subfamily of the lipocalin/cytosolic fatty-acid binding protein family a characterisitc of which is a large beta-barrel ligand-binding cavity. Lipocalins are mainly low molecular weight extracellular proteins that bind principally small hydrophobic ligands, and form covalent or non-covalent complexes with soluble macromolecules, as well as membrane bound-receptors. They participate in processes such as ligand transport, modulation of cell growth and metabolism, regulation of immune response, smell reception, tissue development and animal behavior. Cytosolic fatty-acid binding proteins, also bind hydrophobic ligands in a non-covalent, reversible manner, and have been implicated in intracellular uptake, transport and storage of hydrophobic ligands, regulation of lipid metabolism and sequestration of excess toxic fatty acids, as well as in signaling, gene expression, inflammation, cell growth and proliferation, and cancer development.	1.01394e-87
NZ_CP022412.2|WP_005679142.1|1542192_1543287_-|tryptophan--tRNA-ligase	gnl|CDD|183400	PRK12282, PRK12282, tryptophanyl-tRNA synthetase II; Reviewed.	0
NZ_CP022412.2|WP_005679145.1|1547754_1548306_+|sugar-O-acetyltransferase	gnl|CDD|100047	cd03357, LbH_MAT_GAT, Maltose O-acetyltransferase (MAT) and Galactoside O-acetyltransferase (GAT): MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively at the C6 position of the nonreducing end glucosyl moiety. GAT specifically acetylates galactopyranosides. Furthermore, MAT shows higher affinity toward artificial substrates containing an alkyl or hydrophobic chain as well as a glucosyl unit. Active MAT and GAT are homotrimers, with each subunit consisting of an N-terminal alpha-helical region and a C-terminal left-handed parallel alpha-helix (LbH) subdomain with 6 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X).	1.99116e-86
NZ_CP022412.2|WP_005679144.1|1546975_1547749_+|peroxide-stress-protein-YaaA	gnl|CDD|377151	pfam03883, H2O2_YaaD, Peroxide stress protein YaaA. YaaA is a key element of the stress response to H2O2. It acts by reducing the level of intracellular iron levels after peroxide stress, thereby attenuating the Fenton reaction and the DNA damage that this would cause. The molecular mechanism of action is not known.	7.79764e-106
NZ_CP022412.2|WP_005679146.1|1548771_1550118_+|adenylosuccinate-lyase	gnl|CDD|236452	PRK09285, PRK09285, adenylosuccinate lyase; Provisional.	0
NZ_CP022412.2|WP_005679148.1|1551781_1553185_+|asparagine--tRNA-ligase	gnl|CDD|235176	PRK03932, asnC, asparaginyl-tRNA synthetase; Validated.	0
NZ_CP022412.2|WP_005679151.1|1554575_1554962_+|30S-ribosomal-protein-S9	gnl|CDD|178888	PRK00132, rpsI, 30S ribosomal protein S9; Reviewed.	1.9271e-65

Protein sequences

>NZ_CP022412.2|WP_005679146.1|1548771_1550118_+|adenylosuccinate-lyase
MELDVLTAISPIDGRYRGKTKALAAYFSEFALIKYRVQVEVEYFITLCELPLPQLKGIDNSVFETLRNIYRNFSEADAQRIKDIESVTNHDVKAVEYFLKEEFDKMGGMDDYKEFIHFGLTSQDINNTSVPLSIKEALDKVYYPLIEELIAQLKTYATDWADIPMLAKTHGQPASPTRLGKEVMVFVYRLERQLAMLKACPITAKFGGATGNYNAHHVAYPQYDWKQFGNRFVAEKLGLEREEYTTQISNYDNLSAVFDAMKRINTIMVDMNRDFWQYISMEYFKQKIKAGEVGSSAMPHKVNPIDFENAEGNLGIATSILEHLAVKLPVSRLQRDLTDSTVLRNVGVPFGHIVIAIQSSLKGLRKLLLNEPAIYRDLDNCWSVVAEAIQTILRREAYPHPYEALKALTRTNQAITENSIKEFIEELNVNEDIKKELRAITPHTYTGL
>NZ_CP022412.2|WP_005679145.1|1547754_1548306_+|sugar-O-acetyltransferase
MTEVEKMRNGLLADMSSPELQVRFEHAKKLLARMRGMSTYDEGYRKLLEELVPRIPETSVICPPFYCDHGDGIKLGEHVFVNANCTFLDGGYITIGAHTLIGPCVQIYTPHHPMDYLERRGSKEYAYPVAVGEDCWIGGGAIICPGVTIGDRCVIGAGSVVTKDIPDDSIAVGNPARVIRRRD
>NZ_CP022412.2|WP_005679144.1|1546975_1547749_+|peroxide-stress-protein-YaaA
MLVLLSCAKTMSDVSKVKVPLTTAPRFQKEASEIALQMSQFAVGDLERLLRVNAKIAVENYKRYQAFHAEETPELSALFSYTGIVFKRLNPKDFSASELEYAQEHLRLTSFCYGLLRPLDVIRPYRLEGDVVLPELGNQTMFSYWRSRLTDTFIQDIKQVGGILCNLASDEMRSLFDWKRVEKEVRVVTPEFHVWKNGKLATVVIYTKMSRGEMTRFILKNRIENPEDLKEFSWEGFEFDEALSDERRFVFINGQGG
>NZ_CP022412.2|WP_005679143.1|1543634_1546856_+|carbamoyl-phosphate-synthase-(glutamine-hydrolyzing)-large-subunit
MEKEIKKVLVLGSGALKIGQAGEFDYSGSQALKALKEEGISSVLVNPNIATIQTSEGIADKVYFLPVTTYFVEEIIKKERPDGILLAFGGQTALNCGAELYTQGILDKYGVKVLGTSVEAIMYTEDRDLFVKKLDEINMKTPVSQAVESMEDAIAAARKIGYPVMVRSAYALGGLGSGICANEEEFLKLAESSFAFSKQILVEESLKGWKEIEFEVIRDANDHCFTVASMENFDPLGIHTGESIVVAPTCSLDDKELKLLQELSTKCIRHLGIVGECNIQYAFNSDTDDYRVIEVNARLSRSSALASKATGYPLAFVAAKIALGYSLDQIGEMGTPNSAYVAPQLDYYICKIPRWDLTKFAGVSREIGSSMKSVGEIMSIGRSFEEIIQKGLRMIGQGMHGFVGNDELHFDDLDKELSRPTDLRVFSIAQALEEGYTIDRIHELTKIDPWFLGKLKNIVDYKAKLSTYNKVEDIPADVMREAKILGFSDFQIARFVLNPTGNMEKENLAVRAHRKAMGILPAVKRINTIASEHPELTNYLYMTYAVEGYDVNYYKNEKSVVVLGSGAYRIGSSVEFDWCSVNAVQTARKLGYKSIMINYNPETVSTDYDMCDRLYFDELSFERVLDVIDLEQPRGVIVSVGGQIPNNLAMKLYRQSVPVLGTSPISIDRAENRNKFSAMLDQLGIDQPAWQELTSLEDVKGFVEKVGYPVLVRPSYVLSGAAMNVCYDDEELENFLKMAAEVSKEYPVVVSQFLENTKEIEFDAVAQNGEVVEYAISEHVEFAGVHSGDATLVFPAQKIYFATARRIKKISRQIAKELNISGPFNIQFLARNNEVKVIECNLRASRSFPFVSKVLKRNFIETATRIMLDAPYSRPDKSAFDIDWIGVKASQFSFSRLHKADPVLGVDMSSTGEVGCIGDDFSEALLNSMIATGFKIPEKAVMFSSGAMKSKVDLLDASRMLFAKGYQIYATAGTAAFLNAHGVDTTPVYWPDEKPGAENNVMKMIADHKFDLIVNIPKNHSKRELTNGYRIRRGAIDHNIPLITNARLASAFIEAFCELKLSDIQIKSWQEYK
>NZ_CP022412.2|WP_081447323.1|1543441_1543561_+|methyltransferase
MNQQEIRSKYYLHSDVFHPETAGFFSFLQKRYFSSLVMR
>NZ_CP022412.2|WP_005679142.1|1542192_1543287_-|tryptophan--tRNA-ligase
MGKEKIILTGDRPTGRLHIGHYVGSLKRRVDLQDAGDYSKMFIFIADSQALTDNIDNPEKVRQNVIEVALDYLACGIDPSKATIFIQSQIPELCELSFYYMDLVSVSRLQRNPTVKSEIQMRNFEASIPVGFFTYPISQAADITAFRATTVPVGEDQEPMLEQAREIVRRFNYIYGETLVEPEILLPDNAACLRLPGTDGKAKMSKSLGNCIYLSEEPEEIQKKIMSMYTDPGHLRVQDPGKIEGNTVFTYLDAFCRPEHFERYLPDYPNLAELKAHYQRGGLGDVKVKRFLNAIMQETLEPIRNRRKEFSKDIPAVYEMLQKGCEVARAAAAETLADVKKAMKINYFDDKELIEEQVKRFSQE
>NZ_CP022412.2|WP_005679138.1|1541213_1541684_-|hypothetical-protein
MKHLTLFFAFGALLFLSCQTVSARGVKIPFGDREVLNKVADLPDTEEYKTDNGNYIDLGTIHQEFNIAYILPLYIEQEPRLVGYCEKEDTYYELTEEQLSAILKENNLDGEKLNKVGFYSRYGGKIVGLIIIALIIWGFIPSKKKKTEPGRSIKHT
>NZ_CP022412.2|WP_005679137.1|1540484_1541186_-|hypothetical-protein
MSIYTLIPIIFIVLYAGYWYYVKNKNSQQAQVVNNTDFKAEFANAERYKNSVLTSELPFLQEEMKQEKIDAFNYASTEYGVGSALKDGVKDKLKGMATLGTVRFNTVQTPKYLVLSGNSLHLFDTDTEGEIDRHLVFNQSRLENSRLTEIPMEGQVKAQAQARGNNVKAYKLSLQTDDKPIELIIYSCLIFTNIPEIPTDPQETVQAIVIGNDFLKQLGDRYPNLKVSLPIFS
>NZ_CP022412.2|WP_005679136.1|1539468_1540107_-|DsbA-family-protein
MAISFDWYENPVSPDKPEEKRFHPRIIANGQIDTKDLRSRIQSRCTLNEVDVTAVLDALSQVMGEELCEGRQVHLDGIGYFYPTLTATEEIAADTPRRNTKVKLKGIQFRSDQKLKNSVGHIKIKQMKRIIHSPKLSETDIDSRLRKYFTDHQIMQRSDFQDITGMVRSTAMIHIRRLRTKGKLLNIGIPSQPIYVPAPGFYGKPADYQPVK
>NZ_CP022412.2|WP_032855465.1|1537383_1539372_-|family-20-glycosylhydrolase
MKSPLIIVCCLLMVCVFATAQEPCPQVIPALQQWKGGKGELALPAEGSIVLSPADEATLSPTAQILAQDLKELFGWNYVIKTGKPVGKDICLSLSKPDKELGEEGYTLTVNRYAGIAAPTGQGVFWGTRTLLQILHNEQGKLPKGTARDYPLFPNRGFMLDVARKFFTMDYLKQYVKILSFYKMNEFQIHLNDNGFPQFFGDDWNRTYAAFRLESERFPGLTAKDGSYSKQEFIDLQRMGLEYGVRIIPEIDIPAHSLAFAHYKPEIASRKYGMDHLDLYKKETYQFVDSLLDEYLSGDNPVFIGDLHIGTDEYNKKEAEQYRYFTDRYLKFVEKYGKNVRMWGGLKWLPGKTPVKAEGVTVNAWSYDWVDPVVSLQDGYKLINTCDTYLYIVPAAGYYRDFLDHQWIYEKWSPWIMNRKQTLPEGTPGVLGGMFAVWNDKCGNGISEQDVHLRSFPAMQVLAEKLWKGENKNVTYEAFAKLCKTTPEAPGINLLGKVPAETALTEAGKELSFNGKEAVSTPLQEVGYPYSVEFQLCPEKTNPISSILFQGPHSVVYTNWENTRRIAFSRDGYTFVFNSYRLPADQWTTIRIEGDYKGTSLYINGALQERLEGRTMQVYRKEYDRMEHMTYQETLIFPLQQIGDSRNGFKGKLKNILVRQQH
>NZ_CP022412.2|WP_005679148.1|1551781_1553185_+|asparagine--tRNA-ligase
MEKIGRTKIVDLLKRTDIGAMVNVKGWVRTRRGSKQVNFIALNDGSTINNLQVVVDLANFDEEMLKLITTGACISVNGEMVESVGSGQKVEVQAREIEVLGTCDNTYPLQKKGHSMEFLREIAHLRPRTNTFGAVFRIRHNMAIAIHKFFHDRGFFYFHTPIITASDCEGAGQMFQVTTMNLYDLKKDERGSISYDDDFFGKQASLTVSGQLEGELAATALGAIYTFGPTFRAENSNTPRHLAEFWMIEPEVAFNDIADNMDLAEEFIKYCVKWALDNCADDVKFLNDMFDKGLIERLQGVLKDNFVRLPYTDGIKILEEAVAKGHKFEFPVYWGVDLASEHERYLVEEHFKCPVILTDYPKEIKAFYMKQNEDGKTVRAMDVLFPKIGEIIGGSERESDYDKLMTRIEEMHIPMKDMWWYLDTRKFGTCPHSGFGLGFERLLLFVTGMSNIRDVIPFPRTPRNADF
>NZ_CP022412.2|WP_005679149.1|1553324_1553816_+|DUF4488-domain-containing-protein
MKKLYFFTMLSIMLLAVTGAMAQKKTKFKVAELKGIWQLCHYVSESPDVPGELKPSNTFKVLSDDGRIVNFTIIPGSSAIVTGYGSWKQLTDDSYRESIEKNIHLPMLDNQDNILEFEIKDSDYLHLKYFIKNDLNGNELNTWYYETWKRISMPAKFPEDIVR
>NZ_CP022412.2|WP_004314716.1|1554107_1554569_+|50S-ribosomal-protein-L13
MDTLSYKTISANKATVTKEWVIVDATDQTLGRLGAKVAKLLRGKYKPNFTPHVDCGDNVIIINADKVKLTGNKWNDRVYLSYTGYPGGQREMTPARLIAKPNGEERLLKKVVKGMLPKNILGAKLLNNLYVYAGSEHKQAAQNPKMIDINSYK
>NZ_CP022412.2|WP_005679151.1|1554575_1554962_+|30S-ribosomal-protein-S9
MEVVNALGRRKRAIARIFVSEGTGKITINKRDLAEYFPSTILQYVVKQPLNKIGAAEKYDIKVNLCGGGFTGQSQALRLAIARALVKINAEDKAALRAEGFMTRDPRSVERKKPGQPKARRRFQFSKR
>NZ_CP022412.2|WP_005679152.1|1555082_1555919_+|30S-ribosomal-protein-S2
MSRTNFDTLLEAGCHFGHLKRKWNPAMAPYIFMERNGIHIIDLHKTVAKVDEAAEALKQIAKSGKKVLFVATKKQAKQVVAEKAQSVNMPYVIERWPGGMLTNFPTIRKAVKKMATIDKLTNDGTYSNLSKREILQISRQRAKLDKTLGSIADLTRLPSALFVIDVMKENIAVREANRLGIPVFGIVDTNSDPSNVDFVIPANDDATKSVEVILDACCAAMIEGLEERKAEKIDMEAAGEAPANKGKKKSAKARLDKSDEEAINAAKAAAFLKEDEEA
>NZ_CP022412.2|WP_005679153.1|1556040_1557033_+|elongation-factor-Ts
MAVTMADITKLRKMTGAGMMDCKNALTEAEGDFDKAMEIIRKKGQAVAAKRSEREAAEGCVLAKTTGDRAVIIALKCETDFVAQNADYVKLTQDILDLAVANKCKTLEEVKALPMGNGTVQDAVVDRSGITGEKMELDGYMTVEGVCTAVYNHMNRNGLCTIVAFNKEVNDQLAKQVAMQIAAMNPIAIDEDGVSEEVKQKEIEVAIEKTKAEQVQKAVEAALKKANINPAHVDSEEHMESNMAKGWITAEDVAKAKEIIATVSAEKAAHLPEQMIQNIAKGRLGKFLKEVCLLNQEDIMDAKKTVREVLAAADPELKIVDFKRFTLKAE
>NZ_CP022412.2|WP_005679154.1|1557103_1557613_-|TlpA-family-protein-disulfide-reductase
MKKVTLFCAAALFSLLSFAQNDKGDIVKTGDKMPAFTLTSTVNGTVNSADLKGKVVLINIFATWCGPCQSELAEVQKTLWPKYKDNKDFRMIVIGREHTDEELTAYNKRKEFTFPLYPDPKREVTNKFASQYIPRSYLINKEGKVISATVGYQKEEMDKLMKEIDKALK
>NZ_CP022412.2|WP_005679155.1|1557634_1557985_-|translation-initiation-factor
MKKNDWKDRLNVVYSTNPDFGYEMDNDEEQVTLDKDKQNLRVSIDKKNRGGKVVTLITGFVGTENDLKELGKLLKSKCGVGGSAKDGEIIIQGDFKTKVMELLVREGYTKTKGIGG
>NZ_CP022412.2|WP_005679156.1|1558150_1558801_+|redox-sensing-transcriptional-repressor-Rex
MSTYIPKEADKVPEPTLRRLPWYLSNIKLMKEKGEQYVSSTQISKEINIDASQIAKDLSYVNISGRTRVGYNIDALIEVLESFLGFTNMHKAFLFGVGSLGAALLRDSGLHHFGLEIVAAFDVNPELVGKDLNGIPIFHSDDFETKMKEYDVNIGVLTVPINIAQEITNKMVDGGIKAVWNFTPFRIRVPENIVVQNTSLYAHLAVMFNRLNFNEK
>NZ_CP022412.2|WP_005679157.1|1558801_1559416_+|fumarylacetoacetate-hydrolase-family-protein
MKIIAVGMNYARHNKELGHTQINTEPVIFMKPDSAILKDSKPFFIPDFSNEIHYETELVVRINRLGKNIAPRFANRYYDAVTVGIDFTARDLQRKFREQGNPWELCKGFDSSAAIGTFVPVDRYKDIQNLNFNLLIDGKEVQSGCTADMLFKIDDIIAYVSRFVTLKIGDLLFTGTPAGVGPVSIGQHLQGYLEGEKLLDFYIR

Crispr_ID: NZ_CP022412_3

• CRISPR_ID: NZ_CP022412_3
• CRISPR_location: 4126978-4127052
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP022412_3

Consensus_repeat	Method
ATTAAAAATAGAACATTAATTCA	CRISPRCasFinder

spacers of NZ_CP022412_3

>3.1|4127001|29|NZ_CP022412|CRISPRCasFinder
AATGCTTTTATATCATTTTTCTCCGTATA

CRISPR arrays and Neighbor proteins around NZ_CP022412_3

CRISPR arrays

The CRISPR arrays of NZ_CP022412_3

>merge|NZ_CP022412|3|4126978-4127052|CRISPRCasFinder
ATTAAAAATAGAACATTAATTCAAATGCTTTTATATCATTTTTCTCCGTATAATTAAAAATAGAACATTAATTCA

>NZ_CP022412|3|3|4126978-4127052|CRISPRCasFinder
ATTAAAAATAGAACATTAATTCA	AATGCTTTTATATCATTTTTCTCCGTATA
ATTAAAAATAGAACATTAATTCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022412.2|WP_005678345.1|4118509_4119031_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP022412.2|WP_005678326.1|4137919_4139626_+|acyl-CoA-dehydrogenase-family-protein	unknown	unknown	gnl|CDD|173842
NZ_CP022412.2|WP_005678333.1|4129689_4132533_+|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP022412.2|WP_005678339.1|4122881_4123223_+|DUF4907-domain-containing-protein	unknown	unknown	gnl|CDD|374455
NZ_CP022412.2|WP_005678335.1|4127132_4128338_+|DUF4925-domain-containing-protein	unknown	unknown	gnl|CDD|318501
NZ_CP022412.2|WP_005678336.1|4125433_4126639_-|histidine-kinase	unknown	unknown	gnl|CDD|225814
NZ_CP022412.2|WP_005678334.1|4128359_4129676_+|DUF4925-domain-containing-protein	unknown	unknown	gnl|CDD|318501
NZ_CP022412.2|WP_005678327.1|4136893_4137913_+|electron-transfer-flavoprotein-subunit-alpha/FixB-family-protein	unknown	unknown	gnl|CDD|224936
NZ_CP022412.2|WP_005678331.1|4133387_4135268_+|alpha-L-fucosidase	unknown	unknown	gnl|CDD|226195
NZ_CP022412.2|WP_005678346.1|4117438_4118284_-|patatin-family-protein	unknown	unknown	gnl|CDD|132847
NZ_CP022412.2|WP_005678332.1|4132667_4133348_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP022412.2|WP_005678338.1|4123399_4124584_+|aminopeptidase	unknown	unknown	gnl|CDD|367314
NZ_CP022412.2|WP_005678324.1|4141643_4142063_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP022412.2|WP_005681647.1|4120280_4121618_-|DUF4270-family-protein	unknown	unknown	gnl|CDD|379464
NZ_CP022412.2|WP_005678347.1|4115168_4117049_-|GH32-C-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|350134
NZ_CP022412.2|WP_005678325.1|4139880_4141635_+|rhomboid-family-intramembrane-serine-protease	unknown	unknown	gnl|CDD|366759
NZ_CP022412.2|WP_005678328.1|4136018_4136891_+|electron-transfer-flavoprotein-subunit-beta/FixA-family-protein	unknown	unknown	gnl|CDD|238847
NZ_CP022412.2|WP_005681648.1|4121815_4122904_+|hypothetical-protein	unknown	unknown	gnl|CDD|276965
NZ_CP022412.2|WP_005678337.1|4124705_4125434_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225818
NZ_CP022412.2|WP_005678344.1|4119078_4120284_-|hypothetical-protein	unknown	unknown	gnl|CDD|224978

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP022412.2|WP_005678326.1|4137919_4139626_+|acyl-CoA-dehydrogenase-family-protein	gnl|CDD|173842	cd01153, ACAD_fadE5, Putative acyl-CoA dehydrogenases similar to fadE5. Putative acyl-CoA dehydrogenase (ACAD). Mitochondrial acyl-CoA dehydrogenases (ACAD) catalyze the alpha,beta dehydrogenation of the corresponding trans-enoyl-CoA by FAD, which becomes reduced. The reduced form of ACAD is reoxidized in the oxidative half-reaction by electron-transferring flavoprotein (ETF), from which the electrons are transferred to the mitochondrial respiratory chain coupled with ATP synthesis. The ACD family includes the eukaryotic beta-oxidation, as well as amino acid catabolism enzymes. These enzymes share high sequence similarity, but differ in their substrate specificities. The mitochondrial ACD's are generally homotetramers and have an active site glutamate at a conserved position.	5.25293e-163
NZ_CP022412.2|WP_005678333.1|4129689_4132533_+|TonB-dependent-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	9.70265e-31
NZ_CP022412.2|WP_005678339.1|4122881_4123223_+|DUF4907-domain-containing-protein	gnl|CDD|374455	pfam16250, DUF4907, Domain of unknown function (DUF4907). A family of uncharacterized proteins around 110 residues in length and found in various Bacteroides species. The function of this family is unknown.	4.76074e-34
NZ_CP022412.2|WP_005678335.1|4127132_4128338_+|DUF4925-domain-containing-protein	gnl|CDD|318501	pfam16272, DUF4925, Domain of unknown function (DUF4925). This family consists of uncharacterized proteins around 400 residues in length and is mainly found in various Bacteroides species. The function of this family is unknown.	1.30329e-166
NZ_CP022412.2|WP_005678336.1|4125433_4126639_-|histidine-kinase	gnl|CDD|225814	COG3275, LytS, Putative regulator of cell autolysis [Signal transduction mechanisms].	8.49741e-33
NZ_CP022412.2|WP_005678334.1|4128359_4129676_+|DUF4925-domain-containing-protein	gnl|CDD|318501	pfam16272, DUF4925, Domain of unknown function (DUF4925). This family consists of uncharacterized proteins around 400 residues in length and is mainly found in various Bacteroides species. The function of this family is unknown.	3.18469e-158
NZ_CP022412.2|WP_005678327.1|4136893_4137913_+|electron-transfer-flavoprotein-subunit-alpha/FixB-family-protein	gnl|CDD|224936	COG2025, FixB, Electron transfer flavoprotein, alpha subunit [Energy production and conversion].	7.70127e-105
NZ_CP022412.2|WP_005678331.1|4133387_4135268_+|alpha-L-fucosidase	gnl|CDD|226195	COG3669, COG3669, Alpha-L-fucosidase [Carbohydrate transport and metabolism].	1.20972e-54
NZ_CP022412.2|WP_005678346.1|4117438_4118284_-|patatin-family-protein	gnl|CDD|132847	cd07208, Pat_hypo_Ecoli_yjju_like, Hypothetical patatin similar to yjju protein of Escherichia coli. Patatin-like phospholipase similar to yjju protein of Escherichia coli. This family predominantly consists of bacterial patatin glycoproteins, and some representatives from eukaryotes and archaea. The patatin protein accounts for up to 40% of the total soluble protein in potato tubers. Patatin is a storage protein, but it also has the enzymatic activity of a lipid acyl hydrolase, catalyzing the cleavage of fatty acids from membrane lipids. Members of this family have also been found in vertebrates.	1.22172e-122
NZ_CP022412.2|WP_005678338.1|4123399_4124584_+|aminopeptidase	gnl|CDD|367314	pfam03051, Peptidase_C1_2, Peptidase C1-like family. This family is closely related to the Peptidase_C1 family pfam00112, containing several prokaryotic and eukaryotic aminopeptidases and bleomycin hydrolases.	4.39874e-19
NZ_CP022412.2|WP_005681647.1|4120280_4121618_-|DUF4270-family-protein	gnl|CDD|379464	pfam14092, DUF4270, Domain of unknown function (DUF4270). This family of lipoproteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 444 and 534 amino acids in length.	1.42771e-23
NZ_CP022412.2|WP_005678347.1|4115168_4117049_-|GH32-C-terminal-domain-containing-protein	gnl|CDD|350134	cd18622, GH32_Inu-like, glycoside hydrolase family 32 protein such as Aspergillus ficuum endo-inulinase (Inu2). This subfamily of glycosyl hydrolase family GH32 includes endo-inulinase (inu2, EC 3.2.1.7), exo-inulinase (Inu1, EC 3.2.1.80), invertase (EC 3.2.1.26), and levan fructotransferase (LftA, EC 4.2.2.16), among others. These enzymes cleave sucrose into fructose and glucose via beta-fructofuranosidase activity, producing invert sugar that is a mixture of dextrorotatory D-glucose and levorotatory D-fructose, thus named invertase (EC 3.2.1.26). These retaining enzymes (i.e. they retain the configuration at anomeric carbon atom of the substrate) catalyze hydrolysis in two steps involving a covalent glycosyl enzyme intermediate: an aspartate located close to the N-terminus acts as the catalytic nucleophile and a glutamate acts as the general acid/base; a conserved aspartate residue in the Arg-Asp-Pro (RDP) motif stabilizes the transition state. These enzymes are predicted to display a 5-fold beta-propeller fold as found for GH43 and CH68. The breakdown of sucrose is widely used as a carbon or energy source by bacteria, fungi, and plants. Invertase is used commercially in the confectionery industry, since fructose has a sweeter taste than sucrose and a lower tendency to crystallize. A common structural feature of all these enzymes is a 5-bladed beta-propeller domain, similar to GH43, that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	3.7423e-145
NZ_CP022412.2|WP_005678325.1|4139880_4141635_+|rhomboid-family-intramembrane-serine-protease	gnl|CDD|366759	pfam01694, Rhomboid, Rhomboid family. This family contains integral membrane proteins that are related to Drosophila rhomboid protein. Members of this family are found in bacteria and eukaryotes. Rhomboid promotes the cleavage of the membrane-anchored TGF-alpha-like growth factor Spitz, allowing it to activate the Drosophila EGF receptor. Analysis has shown that Rhomboid-1 is an intramembrane serine protease (EC:3.4.21.105). Parasite-encoded rhomboid enzymes are also important for invasion of host cells by Toxoplasma and the malaria parasite.	6.03154e-35
NZ_CP022412.2|WP_005678328.1|4136018_4136891_+|electron-transfer-flavoprotein-subunit-beta/FixA-family-protein	gnl|CDD|238847	cd01714, ETF_beta, The electron transfer flavoprotein (ETF) serves as a specific electron acceptor for various mitochondrial dehydrogenases. ETF transfers electrons to the main respiratory chain via ETF-ubiquinone oxidoreductase. ETF is an heterodimer that consists of an alpha and a beta subunit which binds one molecule of FAD per dimer . A similar system also exists in some bacteria. The homologous pair of proteins (FixA/FixB) are essential for nitrogen fixation. The beta subunit protein is distantly related to and forms a heterodimer with the alpha subunit.	2.65922e-79
NZ_CP022412.2|WP_005681648.1|4121815_4122904_+|hypothetical-protein	gnl|CDD|276965	sd00038, Kelch, Kelch repeat. Kelch repeats are 44 to 56 amino acids in length and form a four-stranded beta-sheet corresponding to a single blade of five to seven bladed beta propellers. The Kelch superfamily is a large evolutionary conserved protein family whose members are present throughout the cell and extracellularly, and have diverse activities. Kelch repeats are often in combination with other domains, like BTB and BACK or F-box domains.	1.79384e-14
NZ_CP022412.2|WP_005678337.1|4124705_4125434_-|response-regulator-transcription-factor	gnl|CDD|225818	COG3279, LytT, Response regulator of the LytR/AlgR family [Transcription / Signal transduction mechanisms].	2.47533e-44
NZ_CP022412.2|WP_005678344.1|4119078_4120284_-|hypothetical-protein	gnl|CDD|224978	COG2067, FadL, Long-chain fatty acid transport protein [Lipid metabolism].	0.000641346

Protein sequences

>NZ_CP022412.2|WP_005678336.1|4125433_4126639_-|histidine-kinase
MERVRKQQLLEQSIYGVIWSVIFFLPLIGEYFAVSGGLEKEEVRTLVRDSWLGILPFFMLFLLNNYVLVPYFLFKKKYWQYTLSLVFAIGVIFLIVPFPMKGRFPKEFRQEPVYHSAKESRRNQIIEMREKARKKETANWELPDQVKYPVEKFQRPEALLKPVPFLYPPITVRYLIHFMIAFLMVGFNIAIKLFFKSFRDEEMLKELEHQRLQSELQYLKYQINPHFFMNTLNNIHALVDIDTGKAKSTIVELSKLMRYVLYEASNKTILLKREVQFLENYIAIMGLRYTDKVSIEMKFPIEVPEVQIPPLLFISFVENAFKHGVSYRNDSFVRVIVQQEEGNRLTFRCTNSNNGRADEQHHGIGLDNIRKRLRLLFGNDYTLSITQDKNKFDVLLIIPLL
>NZ_CP022412.2|WP_005678337.1|4124705_4125434_-|response-regulator-transcription-factor
MKCLAIDDEPLALAQLSDYISRVPFLSLVKPCQDAFEAMKVLSDEDVDLIFVDINMPDLNGLDFIRSLISPPLVIFTTAYSEYAVDGFKLDAVDYLLKPFEFQDLLKAADKARKQFEYKLLEQQSELGNASQVKGDSLFVKSDCRVVRIDINNIRYIEGMSEYVRIFVEGENKPVITLASLQKMEERLPAHFMRVHRSYIVNLRKITEISRLRIIFDKNTYIPVGDNYKERFTEFISKLSFS
>NZ_CP022412.2|WP_005678338.1|4123399_4124584_+|aminopeptidase
MKKSILIAALGLFSLSTMAQDAKPEEGFVFTTVKENPITSIKNQNRSSTCWSFSTLGFVESELLRLGKGEYDLAEMFVVHKTMQDRGANYVRYHGDSSFSPGGSFYDVMYCIKNYGIVPQEVMPGIMYGDTLPVHNELDAVASGYINAIAKGKLSKLTPVWKNGLAAIYDTYLGKCPENFTYKGKEYTPKTFAESLGLNPDDYVSLTSYTHHPFYSQFAIEIQDNWRNGLSYNLPIDEFMAVMDNAVKKGYTFAWGSDVSEQGFTRDGIAVMPDINKESELSGSDMARWTGLTTANKRQIMTTKPHPEIDVTQEMRQVAFDNWETTDDHGMVIYGIAKDQNGKEYFMVKNSWGKSGKYNGIWYASKAFVAYKTMNILVHKDALPKEIAKKLGIK
>NZ_CP022412.2|WP_005678339.1|4122881_4123223_+|DUF4907-domain-containing-protein
MNGKKMTKKNSSRLFVAGILTAAICLAFSVAATSDTHYSIEIIEVNGGYGYQISHNNHITIFQPFIPAISGKKPFMEKEDAKKVGKLVMRRMKTGENYTVTRHDLENLGIKIK
>NZ_CP022412.2|WP_005681648.1|4121815_4122904_+|hypothetical-protein
MKKLQLLLVSVAMLSIFSCSDDDDDTLGVWYRRSDFDGRAREDAAGFVIGNRGYLCGGYRGKDQREKDCWEYNIDNDWWTQCKDMPDDATARNGAAGFAVGSKGYVTTGYTVYKDDDPMHTGGYAYLKDTWEYDPATNEWRQMDDYPGDARINAIAFTIGNYGYVGTGQSKDDKQTKDFYRFDPTAPSGSQWGIVNGFGGQKRTGGLSFIIDNVAYIVGGTNNGQDVTDFWKFDPSKSEENKWTRLREIKNDSSDDYDDDYNSITRTYGCAFVIDGQAYITLGQTSGSSLRNNYWIYDPNTDLWRSSDTEDDFDYTPFEGSARTKAICFSTGKRGIITTGGSSGYYYDDTWELHPYEWEEDD
>NZ_CP022412.2|WP_005681647.1|4120280_4121618_-|DUF4270-family-protein
MRLFITLFYSLLLFCILFSCRDESSSIGAKWVDSSFMNAVTDTCTVTLSTLLSDSLATSGDTVCQIGRYKDNLYGEIKTSFYAEYEVPSHSLNETTEYQFDSITFKWYSSGNYLGDTLVYHRIELFSLSQGISLEDNGYLFNKTNVNYNRNNLLATLSIRPTPGHRNEMHELRLPDEWGKKWFNLMLEDEECMESQERFRAFFKGIAFIPDENGTCINGFQVNDSSFCLTLYYHELKEKPTEQTLVFKASSSLNYTKVEHDRTGTPIESLRAGTDYNLFSSESDHQVYLQGLTGMYINLEFPHLNNLNQKGRLVSIESAVLKLYPIKGTYNGKYPLPKSLTLYTADQNNSTQSVITDLSGNSVQTGNLVEDNVYYEDTHYSFDITSFIQNNLGTAGQSREKLQLFLSDNDFYNTVQGVIFGDSKHPMNDHNNNVSLTIYYKTYTK
>NZ_CP022412.2|WP_005678344.1|4119078_4120284_-|hypothetical-protein
MKRKVLSIFILSANLLNLTAQNMTNSPASMFGLGELSTGEGGIYSGMGGVGIALRGENAYNSANPASLTGLMPQYFFFDLGVSGAYEKYSQSGANNHSFNGNLNNLGAGFRIAPRWYGAIFMAPVSSVGYAISLEQDVAGTNGETVTSLFQGEGGLSKVGISVAHQLWKGLSLGANFSYVGGTITQSESQGSATETNSSYKHTVYVDFGLQYTYEIERDRSLVAGAVYGYSQDLLQDNDHSVSSSSSSGSITEKGKKYRTCLPQFFGVGVSYNTLRWMASADYKFVDWSRLEFSRSSVSFHNQHRLMLGGSYTLGNPYRKPVRLLLGAGIGNSYLSIQNKTTTNYYLSTGINFEYRSRSTLSLGVKYTDQFKVSSGRFQGQKLAFFLNITFSEKTYRAKLK
>NZ_CP022412.2|WP_005678345.1|4118509_4119031_+|hypothetical-protein
MRIQFEIKEKLPEIIEEIMNSGKWQTSVKEELSGRTTVVIRDQAYGSEATIEIYAKSIEIKTAWSKYSYRIFVANDIVWCEYNGAYRGLLEQVLLPTITPKESLLDSDVTESSLYGREHKKLREYAEDNLKLKQFRRENFNEQRNGTAAFDHPKRVYDEFIKEDYVVTPKDNK
>NZ_CP022412.2|WP_005678346.1|4117438_4118284_-|patatin-family-protein
MKNLKIDESTGLVLEGGGMRGVFTCGVLDYFMDHDIRFPYAIGVSAGACNGLSYASRQRGRAKYSNIDLLEKYNYIGLKHLLKKRNILDFDLLFNEFPEHILPYDYETYFASSERFVMVTTNCITGEANYFEEKKDKRRVIDIVRASSSLPFVCPITYVDNIPMLDGGIVDSIPLQRAIADGYTRNVVVLTRNRGYRKDSKDIRVPSFVYRKYPKLREALSRRCAVYNEQLEMVEKMEDEGKIFVIRPQNPVMVDRIERDVQKLTEFYEEGYECARNLIEK
>NZ_CP022412.2|WP_005678347.1|4115168_4117049_-|GH32-C-terminal-domain-containing-protein
MKTTSWMKLCKGAVLALAVSYGLIYCHTNKSKFMLEQKGDSLTLIHITNPTNYILLPIEEAAEESRVRLDIGDAADTDMDIRLAQTKVDYWVPFVLPADAKTVTVRVQKSLGDALCWKEMKLSDTFDPSHTDKFRPVYHHAPLYGWMNNANGLVYEDEEYHLYYQYNPYGSKWGNMHWGHSISKDLMHWEHLAPAIVRDTLGHIFAGSSIVDQENVAGYGTGTILAFYTSASDKNGQIQCLAYSNDNGRTFTKYDKNPILRSSDRRKDFRDPKVFWYAPGNKWIMIVAADKEMRFYDSEDLKDWNYMSSFGEGYGVQPCQFECPDMVELPVDGDTEHKKWALIVNVNPGCYFGGSATQYFIGDFDGTRFICDSKPDVTKWLDWGKDHYATVSFSNMGRRVIVVPWMSNWQYCNNVPTKPFRGVNALPRELGLYTQSGDIYLSAAPVAEVKNLRKETKEIPAFTVANDYHIESLLPDNGGAYELSLDITAEKAEIIGFSLFNDKGEKVDIYFNLPERKLVMDRTKSGIVDFGKNSVTHEIEVHDRRKTISINYIDDFALATWAPVRKENKYRLDIFVDKCSVEIFLNEGKIAMSNLVFPTEPYNRMCFYSKGGTFKVDTFKVHRLSL
>NZ_CP022412.2|WP_005678335.1|4127132_4128338_+|DUF4925-domain-containing-protein
MKNLRKLFCVACAVLFFTSCEETYNDKLFWPGEISQEYGSYIKPYTLDLTYSGEKLIGKTASFKTEDSETGTLTLNGIIPGEVTTPISRIKLNENGEKDAYTFSGTNITMGGVTVKYNGIITPKAMKLSLDVTMAHANNLAHTYAFPAYSHTTNEEATIRNSGASYVNITTKEGAESIAPIVLQMQQMATNILDVLFPYVLKNITLEKDGIVTANYTTSPIDMKEIMEVANAGKTDAEFRGLIGQRTYVSSPKGLAYWNQTGDKAFVVQLNIPAIISLIAENNGQQIDPQLIAGISEALLKSDPARLKLALSTLNMILNNEIITYILKMDDNTFVTLLSWMRNGIPMGISQATKDHTYIYFKKETLTPFINIIDILLKTNLDEVVALFDKMEIGVDLTIQK
>NZ_CP022412.2|WP_005678334.1|4128359_4129676_+|DUF4925-domain-containing-protein
MKKLSILFISFLTVISAFLISCDEDHYGPAPVDVTANYSNKISNPNPNLVLTYNGDAMNGKSVDFSTVTGETAIITLYDILPGEKAIKITSIPLSGDTEGYSFSGNGMGNETLTTFRYEGRVTKGKLTLNISNIQMGNADLWANTYKLPEVVNGVKKILVGDTWGNEYTWQEVDGQVLNASCYFHADVEATESGATTQTWGNGIQNIVSYILPQVLQDITLGADGNVTASYSNDPLSGVDIDVIFGFLETPLTQEMITPNIADRKYIPSPKGFATWFQKDGKLILKLNLANIISSIASSSDTYMDVNIINAIIDAVSQMDAMKVKELLTTLNQSLNNETLGFLVNVNDTSFNAIFNWLTTGIPMQVTSKEGHTYIYLDKEGFTPIAKLLPDLSPLIVSMLPEDMQGLGFIISTFLNGISEAFLSPEKIEFGLELVPNK
>NZ_CP022412.2|WP_005678333.1|4129689_4132533_+|TonB-dependent-receptor
MKKIYILTLLICLTCFGTSFAQTLKGHIYDAKTNEPLVGAAVTYKLHGNQGVVSNINGEYEIKLPEGGVDLVFSYVGYDDVLMPIVINKREVVTKDVYMKESTKLLEEVVVSAGRFEQKLSDVTVSMDVVKSGDIARQAPTDISSTLRTLPGVDIVDKQPSMRGGSGWTYGVGARSQILVDGMSTLNPKTGEINWNTVPLENVEQVEVIKGASSVLYGSSALNGIINIRTARPGLTPKTRFSAYVGIYGDAENDEYQWSDKNFWKDDKYAVKPILRGSLLSGVRNPIYEGFDLSHSRRIGNFDVSGGINLFTDEGYRQQGYNKRFRMGGSLTYHQPDMGLKILNYGFNVDFLSNQYGDFFIWRSPTEVYKPSPFTNMGREENNFHIDPFINYVNPENGTSHKIKGRFYYSADNIVRPTEGSSITDILGNMGTDANTIKNIVNGDYSSLYPALVGIGSGIINGNLDDAMNGAFTSLRNIFPNATTADYCDLISWVMDNGLPDLSGIQNGQLPSDLVPWLSNVINPSRLNPKTQTDKNFDYYLDYQFNKKWNGGAQITTGMTFEHIRYDSAVMDEVYKSDNAALFFQYDQRFWDRLSVSAGVRAEYYRVNNHRREAETKVFGTKIPFRPVFRAGLNYQLADYSFIRASFGQGYRNPSINEKYLRKDIGGVGVYPNPNIKPEKGFNAELGFKQGYKIGNFQGFVDIAGFYTQYKDMVEFQFGLFNNANNTMINSIGDVFQMLTDGKGFGIGAQFHNVSKAQIYGVEISTNGVYNFNKNTKLFYNLGYVYTEPRDADYQERNAVEGLYTDPLQMKEKSNTGKYLKYRPKHSFKTTVDFQWKRINVGANVAWKSKILAVDYLMLDERSKTQNDLMDYVRGILFGYSKGETLATYWKKHNTDYATVDFRFGVKATKEVAFQFMVNNLFNKEYSYRPMAVAAPRTFVLKMDVTF
>NZ_CP022412.2|WP_005678332.1|4132667_4133348_+|hypothetical-protein
MKKQIVLIAILCCTAFAQAQEVFVNADFVSSYIWRGIDSGNACIQPTLGLNWKGLTVYAWGSTEFRNKNNEIDLSLEYEYKNLTLYANNYFTQTEEEPFKYFNYSSHSTGHTFEVGAGYIFSEKFPLSVSWYTTFAGNDYRENDKRAWSSYCELSYPFSVKDVDMSIEAGFTPWEGFYSNKFNVVNIGLSATKELKITSGFSLPIFGKLIANPYEEQVYFVFGLSL
>NZ_CP022412.2|WP_005678331.1|4133387_4135268_+|alpha-L-fucosidase
MKKHPLILCAGITSLLLSACNPVKAPEAILPVPEAKQVEWQKMETYAFVHFGLNTFNDREWGYGDSDPKTFNPAKLDCEQWVKTFVESGMKGVILTAKHHDGFCLWPTQLTEYCIRNTPYKNGQGDIVRELSDACKKYGIKFAVYLSPWDRNQANYGTPEYVDYFYKQLHELLTNYGDVFEIWFDGANGGDGWYGGAKDSRTIDRKTYYNYPRAYKMIDELQPQAVIFSDGGPGCRWVGNEKGFAGATNWSFLRAGEVYPGYPNYRELQYGHADGNQWVAAECDVSIRPGWFYHPEEDGRVKTVDELTDLYYRSVGHNATLLLNFPVDRDGLIHPTDSANAVNFHKNIQKQLEKNLLAGLSPKASDERGKAFSAKAVTDNDYDTYWATNDDVTSATIEFDLPQPEKINRMMLQEYIPLGQRVKSFVVEYNQEGEWLPVKLNEETTTVGYKRLLRFETITTDKLRVRFTDSRACLCINNIEAFYAGATSDTYSAKAEELKSFPFTLSGVDTEEAQKCMDKNDQTACFVNGNTLLIDLGEERTITSFHYLPDQSEYNKGVIAAYEISVGMDSNAVNQVVAKDEFSNIKNNPILQSVYFTPLKARYVKLKATRMIHDGEPLGLAEIGIQ
>NZ_CP022412.2|WP_005678328.1|4136018_4136891_+|electron-transfer-flavoprotein-subunit-beta/FixA-family-protein
MSLKIVVLAKQVPDTRNVGKDAMKADGTINRAALPAIFNPEDLNALEQALRLKDAHPGSTVTILTMGPGRAADIIREGLFRGADNGYLLTDRAFAGADTLATSYALATAIRKIGNCDIIIGGRQAIDGDTAQVGPQVAEKLGLTQITYAEEILEVGKDKITVKRHIDGGVETVEGPLPIVITVNGSAAPCRPRNAKLVQKYKHAKTVSEKQQGNLDYTDLYDKRDYLNLVEWSVADVNGDLAQCGLSGSPTKVKAIQNIVFQAKESKTISGSDRDVEDLIVELLANHTIG
>NZ_CP022412.2|WP_005678327.1|4136893_4137913_+|electron-transfer-flavoprotein-subunit-alpha/FixB-family-protein
MNNLFVYCEIEEGNVADVSLELLTKGRSLANQLNCQLEAVVAGTDLKDIEKQILPYGVDKLHVFDGEGLYPYTSLPHTAILVNLFKEEQPQICLMGATVIGRDLGPRVSSALTSGLTADCTSLEIGDHEDKKEGKVYKNLLYQIRPAFGGNIVATIVNPEHRPQMATVREGVMKKEILSPTYQGEVIRHDVKKYVADTDYVVKVIERHVEKAKNNLKGSPIIVAGGYGVGSKENFDLLFDLAKELHAEVGASRAAVDAGYAEHDRQIGQTGVTVRPKLYIACGISGQIQHIAGMQESGIIISINNDPDAPINTIADYVINGTIEEVVPKMIKYYKQNSK
>NZ_CP022412.2|WP_005678326.1|4137919_4139626_+|acyl-CoA-dehydrogenase-family-protein
MANYYTDIPELKYHLNNPMMKRICELKERNYRDKDEFDYAPLDFEDAVDSYDKVLEITGEITGEIIAANAEGVDEEGPHCANGRVEYASGTKQNLDAMVKAGLNGMTMPRQFGGLNFPITPYTMCAEIVAAADAGFGNIWSLQDCIETLYEFGNADQHSRFIPRICQGETMSMDLTEPDAGSDLQSVMLKATYSEKDGCWLLNGVKRFITNGDADIHLVLARSEEGTRDGRGLSMFIYDKRQGGVNVRRIENKLGIHGSPTCELVYKNAKAELCGDRKLGLIKYVMALMNGARLGIAAQSVGLSQAAYNEGLAYAKDRKQFGKAIIEFPAVYDMLAIMKGKLDAGRALLYQTARYVDIYKALDDIARERKLTPEERQEQKKYAKLADSFTPLAKGMNSEYANQNAYDCIQIHGGSGFMMEYACQRIYRDARITSIYEGTTQLQTVAAIRYVTNGSYIATIREFEAIPCSPEMEPLMSRLKKMADKFEASTNAVKEAQDQELLDFTARRLMEMAADIIMSHLLIQDASRSSELFSKSAHVYLNYAEAEVEKHANFISNFDKEDLAFYKK
>NZ_CP022412.2|WP_005678325.1|4139880_4141635_+|rhomboid-family-intramembrane-serine-protease
MAFRLRPLHEDTLQFAGLSNTQILILALEASQKLEWNIEELTLEGVRFDVPMSIKSHGEEITVSIQEGSDGEISVRSQSIAMQLVDYGKNRKNIQSLQKAMEEIKSTLSPEELEQKAKKLEDDFNRPLTEEEEAYLKEIEKKSSFISFFIPRKGFIATPILMDLNLLIFILMVAFGVGILEPSTLALLKWGADFGPLTLTGDWWRAITCNFIHIGAFHLLMNMYAFMYIGLWLEDLIGTRRMFISYLLTGVCSAAFSLYMHAETISAGASGAIFGLYGIFLAFLLFHHIPRAQRKALLISILLFVGYNLVYGMKAGIDNAAHIGGLLSGFLLGIIYVISYRFEKKDAQRTISIVGELGIFGIFLFSFLGLCQNIPSTYREIRKEWESGIVEAYLNGELEEENDNQPATNTPSKSSTLQMPPYTPVGNNDTWLSFYDATTNFSCQYPTNWHKITGARGLTPTAEPPFLMLVNGGNQLTAVALTYDTRKEFERIKELTLLLPRNTNGEPSEDYKQSNVTINGLPMTQTSNPLHIGAPDEPGHDVQQIALRYFQEDQLRVFSIVMLVYDKEAQADLEAIVSSIQITK
>NZ_CP022412.2|WP_005678324.1|4141643_4142063_+|hypothetical-protein
MRVYIQVKQLGKRKCCIEKLPVDFSVPPTNVQELIASIVSWQVSKYNDRLQQSEVLQYLTREEVEDKAASGKVGFEVNYNGRPAAETEAIVNALQSYEDGIFRIFIDDTEAGGLSSPVVLKEETTLTFIRLTMLSGRLW

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP022412_3	3.1|4127001|29|NZ_CP022412|CRISPRCasFinder	4127001-4127029	29	NZ_LR214986	Mycoplasma cynos strain NCTC10142 plasmid 13	922997-923025	7	0.759

1. spacer 3.1|4127001|29|NZ_CP022412|CRISPRCasFinder matches to NZ_LR214986 (Mycoplasma cynos strain NCTC10142 plasmid 13) position: , mismatch: 7, identity: 0.759

aatgcttttatatcatttttctccgtata	CRISPR spacer
gatgctattatatcatttttctgatttaa	Protospacer
.***** ***************   *  *

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	1134635 : 1142255	8	Ostreococcus_tauri_virus(16.67%)	NA	NA
DBSCAN-SWA_2	2710220 : 2718149	12	Riemerella_phage(33.33%)	portal	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP022412|1134635:1142255|DBSCAN-SWA
AATGAGAATCGGAATCTTAACATCAGGGGGAGATTGCCCCGGTATAAATGCCACTATTCGTGGCGTGTGCAAAACTGCCATTAACTACTACGGTATGGAAGTGGTAGGTATTCATAGCGGCTTTCAGGGGTTGCTCACAAAAGATGTAGAATCCTTTACAGATAAATCTTTATCGGGTTTGCTGAATCTTGGTGGAACGATGTTGGGGACTTCCCGCGAGAAGCCTTTTAAAAAAGGAGGTGTTATTTCGGATGTCGATAAACCTGCACTGATCCTTCAGAATATTCGGGAAATGGGATTGGATTGTGTTGTCTGTATCGGTGGAAACGGAACGCAAAAGACGGCTGCCAAATTTGCTGCCATGGGTGTAAATATCGTTTCGGTTCCTAAAACCATTGACAACGATATCTGGGGGACGGATATCTCTTTTGGTTTCGACTCGGCTGTAAGTATTGCTACGGACGCTATTGACCGGTTGCATTCTACCGCAAGTTCTCATAAAAGGGTGATGGTGATTGAGGTCATGGGACATAAAGCGGGTTGGATTGCTTTGTATTCCGGTATGGCAGGAGGGGGAGATGTTATTCTTGTGCCTGAAATACCTTATAGCATTAAAAACATAGGAAACACTATTCTGGAAAGATTGAAAAAGGGGAAACCATACTCTATTGTAGTAGTAGCTGAAGGCATTCATACGGACGGCCGTAAACGTGCTGCGGAATACATTGCACAGGAAATAGAGTATGAGACGGGTATTGAAACCCGTGAAACCGTATTAGGGTATATTCAACGTGGTGGTTCGCCTACTCCTTATGACCGTAATCTCTCTACCCGAATGGGCGGACACGCGACGGAACTGATTGCCAACGGGGAATTCGGGCGTATGGTTGCACTAAAAGGAGATACTATCGCTTCTATCCCTTTGGAAGAAGTGGCTGGGAAACTAAAGTTGGTTAGTGAGGATCACGATCTGGTGATTCAGGGACGTCGCATGGGGATTTGCTTTGGATAGATTCCACGATCGGTTCTGCCGTAATCTCATTGTCGAACTCATTTTCTTCCAATATATTGTCATTCAGCAATTCGATATCAGAGTCTGCATCCATTTCGGGTTCAGGTTCGGCTGCCATTGCTGATTGCTGCATTTTGGTTTCGTTGACGGTTGCCATGAAAGTCGGGTCCTTTACTTTCTTTATAGCCATTTGGGCGGCATTCTGTTGGGATTCTTTCTTGGAATATCCGGTTCCGGTTCCGGCAGGAAGTCCTTCAATGCGTACTTCTGTCTGGAAAACAGGATTGCTGTCCTGATCAAGGAATTGCTCAATCAGTTCAAAAGAAACCTCCAGTTTGCTCTTTTGGCTCCATTCGATCAGTTTTGATTTGAAGTTTACTTCTTTACGGGAGATTTTATCCAGATCAATATAACGATTAATGATTCGCTGCTCCATAAACTGTTTGCAGCGTTCATATCCCTGGTCCAGGTAGATCGCTCCGATAAATGCCTCGAAAGCATTCCCGTACATATAGCTGTTGTGGGAAGAAGAACGGGTTGAATATTTAATAAGTTTGTCCAGTCCGATCTCTACGGCAAGTTTGTTTAAAGTCTCCCGTTGTACAATCTTGGAACGTGTGTTTGTCAGGAAACCTTCCCGCTTCCCTTCAAAACGTTTGTAGACGATATCGCCTACGATAGCGTCGAGAATGGCATCACCTAAAAATTCCAGACGCTCATTGTTTAACGGACGCCCCTTGTCCGAACGGACAGATGAGGATTTATGTAAGAGAGCCTGCTCATAGAGCTGGATGTTACGCGGGTAGAAACCGAGTATCCGGTAAAAACAAAGATAAGACTCTCTATCCCTGTGGAACAAGAGCCTTATCTTATCTATTTGGTTTCGTAACACGATTTTACTCAGCGTATTTTTTGAAGATAACGCACGCATTATGACCGCCGAATCCGAATGTGTTGGACAAGGCAACATTAACTTCGCGTTTCTGTGCTTTATTGAACGTGAAATTAAGGTTATAGTCGATATTTTCGTCGTCGTCACCTTCTTCATGGTTGATAGTCGGGGGAACAATGCCGTTCTTGATGGCAAGGATACTTGCAATTGATTCTACCGCACCGGCAGCACCCAGCAAGTGACCTGTCATTGATTTTGTTGAACTGATGTTCAACTCGAACGCATGATCACCGAATACTTCTTTAATCGCTTTTGCTTCCGAAATGTCACCAACCGGAGTAGATGTACCGTGTACATTGATATAATCCACTTCTTTCGGGTCCATTTCCGCATCTTCCAATGCATTCATCATCACAAGTTTGGCTCCAAGACCTTCCGGATGAGAAGCTGTCAGGTGATGTGCATCAGCAGACATGCCTACACCGGCAACTTCTGCATAGATTTTAGCACCACGGGCTTTCGCATGTTCTAGTTCTTCCAGAATCAAGCAACCGCCACCTTCGCCCATGATGAAGCCGTCACGGCTTGCACTGAACGGACGTGAAGCCTTTTCGGGCTCGTCGTTGCGGGTTGACAGAGCATGCATAGCATTGAAACCACCTACACCTGCGGGGAAGATAGCCGCTTCCGAACCACCGGATACAATCACATTTGCTTTGCCCAGACGAATCAGGTTAAACGCATCTGCAATGGCATTGGTAGAAGTAGCACATGCCGAACAAGTCGCGTAGTTAGGACCATGGAAGCCATACATGATAGAAATCTGTCCGGCAGCGATATCCGAGATCATCTTCGGGATGAAGAACGGATTAAACTTCGGACCCATTTCCTGACGAGTGTAGTAGTTGCCTACTTCCTCTTCAAATGTATGTATACCACCGATACCGGCGCCAAAAATAACACCGATTCTGTTCAAGTCTTCTTTTTCTACATCAAGACCGGAGTCTGCTACCGCTTCTTTGGCAACTGCAATGGCGTACTGAGTGTACAGATCCATTTTCCTTGCCTCTTTACGATCGATATATTTCGTTACATCGAAGTTTTTCACTTCGCATGCGAATTGGGTCTTGAATAGCGACGCATCAAAATGAGTAATAGGCCCTGCTCCACTAACCCCGTTCACAATATTCTCCCAAAATTCGGGCACACCATTGCCAACAGGAGTAATGGCGCCAAGGCCTGTTACTACCACTCTTTTTAATTCCATATTGATGAAATCGGATAATTACTTAGCGTGTTCTTCGATATAAGATACAGCATCACCTACAGTACCAATCTTTTCTGCTTGGTCATCAGGAATAGAGATACCGAATTCTTTTTCGAATTCCATGATAAGTTCTACAGTGTCAAGAGAATCTGCTCCCAGGTCGTTAGTGAAGCTTGCTTCGGTTGTAACTTCTGATTCCTCTACGCCTAATTTATCAACGATAATCGCTTTTACTCTTGATGCAATTTCAGACATAACTTTAAGTTTTTAATTAATAATTAGTTTTATTTCTTTAAATTTGCGGTGCAAAGGAATGAATATTTATCGTTTTGCGCAAATATTTGACTAAATAAATGCAATGTTTTGCACATTTTTCACTGTTTTGTGCATTGAAATCGAGAGTTATGAAGAAAAACATCGCTATTTTCGCTTCCGGTTCCGGCTCTAATGCCGAGAATATTATCCGGTATTTCCAAAAGAATGACTCTGCTCAGGTGTCATTGGTGCTTTCCAACAAAAGTGATGCCTATGTTTTGGAGCGTGCACACCGTCTAGGAGTGCCCTGTAACGTGTTTACAAAGGAAGATTGGATAGCCGGAGATGAAATTCTGGCTGTTTTGCAAGAGTATCGAATTGATTTTATTGTGTTGGCAGGATTCCTTGTCCGCGTGCCGGATTTACTTTTGCATGCTTATCCCGATAAAATCATAAATATACATCCTGCACTTCTTCCGAAGTTCGGCGGGAAGGGGATGTATGGAGATCGTGTTCACCAGGCTGTGGTTGCTGCCGGTGAAAAAGAAAGCGGTATTACTATACATTATATTAATGAACACTATGATGAAGGAGATACGATCTTTCGGGCGACCTGTCCCGTTCTTCCGACAGATTCTCCTGGGGATGTCGCTGAGAAGGTACACGCTTTAGAGTACGAACATTTCCCACGAGTAATAGAACAGATTATAACGACGTTATAATCCCCACACTAAATTAGCCTTCTAAACTGTTATGTTGTTCAATTCAATAGAATATGTAATATTCTTGCCATTGTTTTTTATCGGATACTGGTTTATTTTTAAACGTTTGAAATTACAAAATATATTTGTTGTAATCAGTAGTTATATCTTTTATGGTTGGTGGGACTGGCGTTTTCTAATTTTAATAGCATTTACTACTTTGTGTAGTTATGCTAGCGGAATCCTGATAGAGCGGCAAGAACGTCGTTTGATTCAACGATGGATATGTGCGGCTAATATTACATTGAATTTGTTGGTGTTATGCATATTTAAGTACTTTAATTTCTTTTCTGAGAACTTTGTGTCCTTATTTGAGACTTTCGGGATTAAGTTGGATTGGGTAACATTAGATATTCTGCTTCCTGTTGGAATCAGCTTTTACACTTTTCAGGCTCTCAGCTATACTATTGATATATATCAGCATAAAATGAAACCGACACATGATATGGTGGCATTTTTTGCTTTTATCAGTTTCTTTCCTCAATTAGTGGCAGGTCCTATCGAAAGGGCTACTAACTTGTTGCCGCAGTTCTTGAAAGTTCGCACGTTCGATTATGGACAGGCAGTAGACGGAATGCAGCAGATACTGTACGGGTTATTTAAGAAAATGGTGATAGCCGATAATTGTAGCCGATTGGTCGATATCGTTTTTAGCAATTACCAACAGTTGGGAAGCATACAACTATTTTTAGGAGCTGTCTTCTTCACCTTTCAAATCTACTGTGATTTTTCCGGTTATTCGGATATAGCTATCGGTACAGCCAAGTTGCTCGGGATTAAATTAATGAAGAATTTCGATTATCCGTATATCTCGCGTAATATAGCGGAGTTTTGGAGAAGATGGCATATTTCGCTAACGACATGGTTTAGAGATTACATTTATATTCCTTTAGGCGGAAGCCGGGTAGGGAAGTGGAAAAGTGTGCGGAATACTTTTATTATATTTCTCGTAAGCGGCTTCTGGCATGGAGCTAACTGGACATTTATTTGCTGGGGACTTTTCCATGCTTTATTATTCCTGCCTTTATTACTGACTTCTTCCAATAGAAAATATCGTGGCATTGTGGCAGAAGGAAAACTTCTTCCTTCCTGGAAGGAGGCTATTCAGATAGGAACAACATTTTTTCTGGTAGTAATCGGCTGGATACTGTTCCGGGCAGAAAATATGGAACAAGCTATCGGCTATATCGGACGACTTTTTTCTATGCAACAGTCTACCGGCAATATGCCTTCCCACTCTTTGGAGGTAGGATTGTATATTCTGCTTTTCTGGATTCTGGAATGGTTTCAGCGAGATAAGCCATATGCGTTGCAGATTCAGTTTCTAAAAAGTAAATCATTGCGCGTTGCTATCCTGACGTTTGTAATCTTATTCATAGAGATAACCATGGGTAAGTCCTCGGAGTTCATTTATTTTCAATTCTAAATAAGGAATATGAGAAAGTTCTTAAGAAATCTTCTTTTAGCATTAATTCCCGTAGCTGTTATTAATGCATTGTGTTGGGGAACGTTGGTCTTTTTAGCATGGCAAGATGATTTGACATATGTGAATTATGCGTCTGCACTGGATAAAGAAAAGCGTTTGGAAGAATTGGGAAATCAGTCCCGCTTGCTAATAATAGGTGGTTCTAACGCCCGCTTTGGCTTTGATTCTTCCATTCTGAGAGATACATTACATCTGGAACCTGTGAATATGGGAATACATATCGGGTTGGGATTGAATTATATGTTTGAGGAGGTTTACGACCATTTACGAAAAGGAGATGTGTTGCTCGTTTCTGCAGAATATAATCATTTTCTTAAGGAGGGCAGTTATTATGGGGATGAAGGTCTGACTGATATGTATCTGATAAAGCATGAATGGGGAAAGGCCTTATATAATATGGTAAATACACATAATTTTTTTTCGATGTATCGCTTGATTCGTAAACGTGTAAAACGGATAGGTATGGATATAGAAGATATACCGGAGAATATGGAAGTTCGTACTAAATATAATGAATATGGTGATTATACCGGACATTATAATCTATCTTCTGCCGGACATTGGGACAGTGCCCCATTACCTATGGTATCACCCGATGAAAAAGTTTTTATAGATTTGAAAGAGAAAATATCTACTTTAAGTGAGCGGGGGGTGACTATTTTCTTCTTGCCTCCTCCATATTGTCGTTCTTCTTTTCAAAATGATTCTTTGGCCATTAACCGTATCTCGGAGAGTTTGAAGGCTATAGGCTTTCCTTATTATTTGGAACCTTCCGGTTGTGTTTATCCTGATAGTATGTTCTATGACTCGCGTTATCATCTGATTAGGGAAGGTGTGGTGATGCATTCTCGGAAGATAGCAGGTGAGTTGAAAAGAACTTTATAAATATATGTGAGAAATTGTTTTATTCAATTTTTATTATGTAGGCTTTTTCTTCTCTTCGTAACGGATAGTTTCCCCGTAATTCTTCAAACAGTTCCGGTTGAGCTTTCAGCCGGTCGCTGTCTTCGACAGGGTTATATATTTGGAGCAATGCTTCTTCCTGACTTTGTGCATGAATGATAGGAGAGGTAGGTGCGGGAGCGTTAATTTCATACTTTCCCTCTATATGGAAGAACTTACAGATTGCATCCAGCGACATTCGCGTTGCATTAGCCTTGCCGTCAGCGGAATATCCGGCAATGTGTGGAGTGCCGATAATCACTTTCTCTAATAATTCACGATTGATTTCCGGTTCGTGTTCCCATACATCAATAATAGCGTCTGAGATAGAACCATTGTTCAATGCCTTCAAGAGAGTGTCCGTGTCGATAACTTCTCCTCGTGAAGTATTAATGATAACAGGTTTGCGTTTTAGCGAATTGAAGAAATCTTCATCTGCCAGGTGGAATGTTTTGTATTTGCCTTCTTTATATAAAGGTACATGAAAAGTGATGATGTCACATTCTTCCGCTATCTTATTTAAAGAGGTAAAGGATTCTTTTCCTTCTTTTTCTTCCCGTGGCAGATCGTTCAGTAGAACGCGTATGCCGAAGTCTTCGGCGACTTTGGCAACTTTACTCCCCACATTTCCTACTCCTACGATTCCAATAGTCAGTTCGTCCAGTTTCTTATTTCTGAGAGACTTCCATATCAGGAGTGAAGATTGAATATATTGGGCAACAGAAGCTGAGTTGCAACCGGGTGCATTTGTCCATTCGATACCTGCCCGCTTACAATATTCAGTATCGATATGGTCGAACCCTATGGTTGCCGTAGCTATAAACTTTACCCGGCTGCCTTCCAGTAATTCCTGATTGCAGTGAGTACGGGTCCGGATAATCAGCGCATCTGCGTCTTGTACCAGTTTCGGAGTAAAATCCTTTCCGGGGGCGTAGATTATTTCGTCGGCTATTGTCTGGACAGCCTCTTTTATATAAGGTATCTTATTATCGATAATAATTTTCAT

Protein sequences of DBSCAN-SWA_1

>NZ_CP022412|1134635:1142255|1137823_1138060_-|WP_002558672.1|DBSCAN-SWA
MSEIASRVKAIIVDKLGVEESEVTTEASFTNDLGADSLDTVELIMEFEKEFGISIPDDQAEKIGTVGDAVSYIEEHAK
>NZ_CP022412|1134635:1142255|1138813_1140247_+|WP_005676986.1|DBSCAN-SWA
MLFNSIEYVIFLPLFFIGYWFIFKRLKLQNIFVVISSYIFYGWWDWRFLILIAFTTLCSYASGILIERQERRLIQRWICAANITLNLLVLCIFKYFNFFSENFVSLFETFGIKLDWVTLDILLPVGISFYTFQALSYTIDIYQHKMKPTHDMVAFFAFISFFPQLVAGPIERATNLLPQFLKVRTFDYGQAVDGMQQILYGLFKKMVIADNCSRLVDIVFSNYQQLGSIQLFLGAVFFTFQIYCDFSGYSDIAIGTAKLLGIKLMKNFDYPYISRNIAEFWRRWHISLTTWFRDYIYIPLGGSRVGKWKSVRNTFIIFLVSGFWHGANWTFICWGLFHALLFLPLLLTSSNRKYRGIVAEGKLLPSWKEAIQIGTTFFLVVIGWILFRAENMEQAIGYIGRLFSMQQSTGNMPSHSLEVGLYILLFWILEWFQRDKPYALQIQFLKSKSLRVAILTFVILFIEITMGKSSEFIYFQF
>NZ_CP022412|1134635:1142255|1141211_1142255_-|WP_005676988.1|DBSCAN-SWA
MKIIIDNKIPYIKEAVQTIADEIIYAPGKDFTPKLVQDADALIIRTRTHCNQELLEGSRVKFIATATIGFDHIDTEYCKRAGIEWTNAPGCNSASVAQYIQSSLLIWKSLRNKKLDELTIGIVGVGNVGSKVAKVAEDFGIRVLLNDLPREEKEGKESFTSLNKIAEECDIITFHVPLYKEGKYKTFHLADEDFFNSLKRKPVIINTSRGEVIDTDTLLKALNNGSISDAIIDVWEHEPEINRELLEKVIIGTPHIAGYSADGKANATRMSLDAICKFFHIEGKYEINAPAPTSPIIHAQSQEEALLQIYNPVEDSDRLKAQPELFEELRGNYPLRREEKAYIIKIE
>NZ_CP022412|1134635:1142255|1138158_1138782_+|WP_005682440.1|DBSCAN-SWA
MQCFAHFSLFCALKSRVMKKNIAIFASGSGSNAENIIRYFQKNDSAQVSLVLSNKSDAYVLERAHRLGVPCNVFTKEDWIAGDEILAVLQEYRIDFIVLAGFLVRVPDLLLHAYPDKIINIHPALLPKFGGKGMYGDRVHQAVVAAGEKESGITIHYINEHYDEGDTIFRATCPVLPTDSPGDVAEKVHALEYEHFPRVIEQIITTL
>NZ_CP022412|1134635:1142255|1135587_1136577_-|WP_005676980.1|DBSCAN-SWA
MRALSSKNTLSKIVLRNQIDKIRLLFHRDRESYLCFYRILGFYPRNIQLYEQALLHKSSSVRSDKGRPLNNERLEFLGDAILDAIVGDIVYKRFEGKREGFLTNTRSKIVQRETLNKLAVEIGLDKLIKYSTRSSSHNSYMYGNAFEAFIGAIYLDQGYERCKQFMEQRIINRYIDLDKISRKEVNFKSKLIEWSQKSKLEVSFELIEQFLDQDSNPVFQTEVRIEGLPAGTGTGYSKKESQQNAAQMAIKKVKDPTFMATVNETKMQQSAMAAEPEPEMDADSDIELLNDNILEENEFDNEITAEPIVESIQSKSPCDVPESPDRDPH
>NZ_CP022412|1134635:1142255|1136542_1137805_-|WP_005676981.1|DBSCAN-SWA
MELKRVVVTGLGAITPVGNGVPEFWENIVNGVSGAGPITHFDASLFKTQFACEVKNFDVTKYIDRKEARKMDLYTQYAIAVAKEAVADSGLDVEKEDLNRIGVIFGAGIGGIHTFEEEVGNYYTRQEMGPKFNPFFIPKMISDIAAGQISIMYGFHGPNYATCSACATSTNAIADAFNLIRLGKANVIVSGGSEAAIFPAGVGGFNAMHALSTRNDEPEKASRPFSASRDGFIMGEGGGCLILEELEHAKARGAKIYAEVAGVGMSADAHHLTASHPEGLGAKLVMMNALEDAEMDPKEVDYINVHGTSTPVGDISEAKAIKEVFGDHAFELNISSTKSMTGHLLGAAGAVESIASILAIKNGIVPPTINHEEGDDDENIDYNLNFTFNKAQKREVNVALSNTFGFGGHNACVIFKKYAE
>NZ_CP022412|1134635:1142255|1134635_1135646_+|WP_005676979.1|DBSCAN-SWA
MRIGILTSGGDCPGINATIRGVCKTAINYYGMEVVGIHSGFQGLLTKDVESFTDKSLSGLLNLGGTMLGTSREKPFKKGGVISDVDKPALILQNIREMGLDCVVCIGGNGTQKTAAKFAAMGVNIVSVPKTIDNDIWGTDISFGFDSAVSIATDAIDRLHSTASSHKRVMVIEVMGHKAGWIALYSGMAGGGDVILVPEIPYSIKNIGNTILERLKKGKPYSIVVVAEGIHTDGRKRAAEYIAQEIEYETGIETRETVLGYIQRGGSPTPYDRNLSTRMGGHATELIANGEFGRMVALKGDTIASIPLEEVAGKLKLVSEDHDLVIQGRRMGICFG
>NZ_CP022412|1134635:1142255|1140256_1141192_+|WP_005676987.1|DBSCAN-SWA
MRKFLRNLLLALIPVAVINALCWGTLVFLAWQDDLTYVNYASALDKEKRLEELGNQSRLLIIGGSNARFGFDSSILRDTLHLEPVNMGIHIGLGLNYMFEEVYDHLRKGDVLLVSAEYNHFLKEGSYYGDEGLTDMYLIKHEWGKALYNMVNTHNFFSMYRLIRKRVKRIGMDIEDIPENMEVRTKYNEYGDYTGHYNLSSAGHWDSAPLPMVSPDEKVFIDLKEKISTLSERGVTIFFLPPPYCRSSFQNDSLAINRISESLKAIGFPYYLEPSGCVYPDSMFYDSRYHLIREGVVMHSRKIAGELKRTL

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_005676979.1|1134635_1135646_+	6-phosphofructokinase	H8ZJH0	Ostreococcus_tauri_virus	6.4e-13	28.7
WP_005676980.1|1135587_1136577_-	ribonuclease III	A0A0P0YM82	Yellowstone_lake_phycodnavirus	1.8e-23	33.8
WP_005676981.1|1136542_1137805_-	beta-ketoacyl-ACP synthase II	NA	NA	NA	NA
WP_002558672.1|1137823_1138060_-	acyl carrier protein	A0A1P8VWH3	Flavobacterium_phage	5.7e-05	35.6
WP_005682440.1|1138158_1138782_+	phosphoribosylglycinamide formyltransferase	M4QRX9	Synechococcus_phage	1.5e-20	33.2
WP_005676986.1|1138813_1140247_+	MBOAT family protein	A0A125RNP0	Pseudomonas_phage	9.0e-61	33.5
WP_005676987.1|1140256_1141192_+	hypothetical protein	NA	NA	NA	NA
WP_005676988.1|1141211_1142255_-	4-phosphoerythronate dehydrogenase PdxB	A0A1J0F959	Only_Syngen_Nebraska_virus	2.4e-23	27.0

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP022412|2710220:2718149|DBSCAN-SWA
TATGGCAGGTAGAGGTAGGCCCAAATTAGAGATGTCTCTTTATGATAAATATATAAAAGGTAAAGAGGATATTATTATAGCAGACTGTAGGAATGGAGCTGATAACAAAGGTTTATGTGTACGTCTTGGAATAGGACTTACTACATTTAAAAGTATATTAAAAAAGCATCCTGAAGTTGTAGATTTATTGAGAGAAGGTAAGGAAGAAGCTGACATGAAAGTAGAGAGTGCTTTATATAAAAGAGCTATTGGCTATGATATCGAGGAAACTACAACTGAAGTGAGAATAGGAGAGGACGGATCAGGTCAAACTACCGTTGTTAAGAAGACGAAAAAGCATGTCGCAGGAGATACAACGGCACAAATATTCTGGTTGAAAAATCGTAGGCCAAATGAATGGAAAGATAAACAGGATGTAAACGTAACTAACAATGATTGGGTAGATGCTTTAAAATCATTAACCACTTCATATAAGAATGGTGACAAAGGATGAAAAGAAGGAACTAATCAGTGAAATTATAGCATACTGGTCTAATGACTGGAATAAGTTCGTTCGTGACGCATTATGTGCAAGATTAGATCGTGAGCAGCAAGCTATTATTGAGTCTGTTCAGCATAATCCAATGACTGCTGTTGCAAGTGGAACTGCTCGTGGAAAAGATTTTGTTGCTGCCTGTGCTTCGCTATGTTTTATGTATCTAACTCCTAGATTTAATGAAAAAGGTGTGCTTGTTGGGAATACTAAGGTGGCTATGACAGCACCAACAGGGCGGCAAGTGAAAAATATTATGACTCCTGAAATAAGAAGGCTGATTCGTGCTGCAAGGACAAAGTTCCCTTTTTGTTGTCCTGGCAGATTGGTTGCTGATGATATAAGAACGGATTATGAAGAATGGTTTCTGACAGGATTTAAAGCGGATGATAATGCAACCGAATCATGGTCTGGATTTCATGCAGCGAATACCATGTTTGTTATCACGGAGGCATCAGGTATATCCGAAATTGTTTATAATGCAATAGAAGGTAACTTGCAGGGCAATTCTCGGATGCTCATAGTATTTAACCCGAATATTACTACTGGTTACGCAGCTCGTGCCATGAAGTCTGACCGTTTTGCGAAATTCAGGCTTAGCTCTCTAAATGCAGAAAATGTAGTAAAGAAGCAAATAGTAATACCCGGTCAAGTGGATTATGAATGGGTTAAGGACAAGGTTATAAATTGGTGCTCCCCCATTCAACAAACGGACTTCAATGAGGGAGAAGGAGATTTTAATTGGGAAGGTAAGCTATACCGACCTAACGATTTGTTTCGCGTCAAGGTACTTGGTATGTTCCCGAAAGTATCTGAAGATGTTCTTATTCCTTATGAATGGATAGAGATAGCAAATAGGAATTGGCAGGAATTACAGGCAAGTGGTTTCATTCCAGCCAAATCTTGTAAGCTAGGTGTTGATGTTGCCGGTATGGGACGCGACAATAGTGTCCTTTGTCCGAGATACGGGAATTATGTTCCACAATTTGATGTTCATCAATCTGCTGGACGTGCGGATCACATGCATGTAGTAGGTATGACAATACCATATTTAAAGAAGAAGGGAGCAAAAGCATTTATTGATACGATAGGAGAGGGGGCAGGTGTCTATTCTCGTTTGTTGGAGGAAGAATTTACGAATGCTTTTTCATGCAAATATTCGGAAGGGACAGATGGATTGCATGATATTACCGGAGAGTACGAATTTGCCAACATGCGTGCATATCTGTATTGGGCTTTACGTGATTGGCTCAATCCTAAAAATGGTTTTGGTGCAGCTTTGCCACCGTGCGACCAGTTGATGGAAGAAGCGACTGAAACCAAGTGGAAATTCCTTAGTAATGGAAAGGTTATTATTGAACCTAAGGAAGATGTCAAAAAACGTATTAAGCGTTCTCCTGACTATATGGACGCATTAGCGAATACGTTTTATCCTAGAAATTATAGTTTTATTAGTGATGAAGAGTTGCTCAAAGATTTTTTGTAGTTGTGTTTCTTTTAGTACCTTTGCCTTTGAAAACACTTCTAATTTGTGTTTTCATTGCTCTTATGTGCACTGGCTTGTGAAAGTCGGTGCCATTTTTGTTCTATGTCAAAAGTTAAATCTTTGATTATGAGTGTTTTATACTTAAAATAATTGTGTAGATATTTGGCTAAATCACTGATAATGAGTATCTTTACAATACTAAAAGAAACCAATATTACTAACAATTAAAAGACAAGAGCAATGAAAGCAACAGCAATCCAACAGAGAATAATAGAAAAATTCATCATGTCAGAGTTTGCACAAGGTAACTTAGATACCAAAGAACAAGTTAGCTGTATGCTTCTACTGATTCAAAAGAAACTAGATATGTCAGTAGAACAAGCAAGTGATTTTATGAGAAACGCAATTGGTATTAACGCTTAATACATACGATTATGAAAGTGTATGATATAAATGGGAACGTAGTAGCAGAAGGATACTTGGTACCCAATCCTAATTTCATTCCCAAAGGTGAATACAAAGAAACAGAACTGGATTATCAAAAGAAGCAAGCTGATATGTTAATAACTTCTATTGATGGCAATTTCTATGAAATCAGTTTGCCTAAAAGTGCTACACTTCGCCAGAAGATAAACAAAGACATACAGGGATATGGTAGAAACGTAAGAAGGTATAATGAAAATATAATTCATGTAACAGAGAAGGTTCTAAAGATTTTGCAAACTAAATATACTATAATGTGTGACTTTTAAAAATAGATATGACACAAGAACGACTTGATATATTTGAAAAAGTACTCTTCCTCTATGGAGAATACGTCTTACTCGATCTTTATTCTTTTGCTAAAGTTACGGAAAGATATGAAGATTGCGCTATCATGAGAGATTTAATGAAGAAGTACAATATTGATGAACGTGATGATATACAAGATTGGCAGGCTGAATTATGGCGTTGTGGATATTCTGGTAAGATTGCTGTCATAAATTTCCCTTATTATATGCATAAAGCTATCAAATTAGTTGGATATTTATAAATAAAAGTGATATAAATTACGCGACTTTTATTATATTTGCACCAAGTAAAAACGAATATTAAGTAATATTCTACTCAAATGGACGAAATCACCTCTATCTTAGACAGTACACGGCCCGTTGATAACATAATCAACGATTTGAAAGAAAAGTCTGTAACAGTCCCCTCATGGGATAAACTTCTCAAAGACTACGAACCAACAGAACATGAGATAGTATCTGACACAGTTACTCGTAAAGACAAGATTCGATCTAATGGAGATATAGAAAAAGCTTCCCGTATCTACATTGGGCTTGAAAAACTTCTCACCAAACGAATGACTGAATTCATGTTTGCTATCCCTGTTAAACGTGTATATCACAATATAGAAGACAATGAAACCCGCCAAAGTATTGCGAAAGCGATTGAAGCGATATATAAGTATTCCCGTATTGACAGTGAAAATATTAAGCGAGGAAATGCTTACTTTGCTTCATGCGAAGTGTTTACCATTTGGTACACAGTTGAGAGTTTCAACACTCTATACGGCTTTAAAAGTAAGTATAAGCTAAAATGTAAGACCTACTCACCAATGGACGGTGTTAGGTTATATCCTTTACTTGATGAGCTTGGCGATATGATTGCAATGTCTTTTGAATACACAAAAAAGGTCAAAAATGTAGAAGTTACGTATTTTGAGACATACACGGCAAATATTCATTATAAATGGGAACAACAAGGAAACGGCTGGGAATTAGTTAAATCAGAACCAGTCGTTATTCTGAAAATACCTGGAGTATACGTTTATCGTCCTGTTCCCATTTATCACGGTCTTTCCTATATCAGAAAAGAAATCGAATACACCCTTTCACGCAATAGCGATGTCATAGCATATAACTCCGCTCCAATCCTAAAAATAGCTGGCGGCATAAAAGGTGGAGAAGATAAAGGAGAAAGCCGTAGAGTTTATCGCGTAGAACAAAACGGGGATGTGTCCTATGTTTCATGGGCACAATCTATCGAAGCGTTAAAATATCATGTCGATACCCTTATTAAGTTATTTTGGTCACAATCACAAATGCCGGATATTTCTTTTGAAAACATGAAGTCTCTTGGCAATATCGGATTTGACGCAAGGCAGACTTTACTTACTGACGCTCATTTAAAGGTTGGAGATGAAAGTGGTGCATGGATAGAAGCATTTGAACGTGAATGTAGCGTAATCAAAGCTTTCCTAAAAATGATGAATGTCTCTTGGAAAGACGAAGTAGATAATGTTGAGGTTGAGCACATCATAACTCCGTTTATTCAAAATGACGAAAAGTCAGAAATAGAAAAGTGGGTTACGGCAAGTGGTGGAAAAGCAGTTGTCAGCCAATTAGAAGCCATCAAGAACTTAGGTATCTCTACTGATCCACAAGATACTCTTTCCCAAATTCAAAAAGAAGATGCAGAGGCTTCCAAAAGCAGGATAAGCAATATTTTCGAACAATCGGAATAATAATCAAAATATAATCATTATGGCAAAAATAGATGTATTAGAATTTAGTAAAGAAAAACAAGGTTATTCCTGTGAATTTACTTCTGTTGGGAAATGTGTAATACAGATAGATAGAGAAATGAATGGGACACTTAGCCTATTTGCAAAATTGGAGGGTATGGATTATGCACTGTTGTATCAATACCCTTCTGCTCAATTTAATGATAATGTGATTTTTGAGCTTGACGTACAAAAGGGGCTTTCTATCAAGATCCTAAGCACAGTCGGTGTTATGAGTGCAAAGATGGCTTATGAAGATGAAGATTTATAACCTATTTGCCAACTTGTAGAAAAGGTAAAGGCAGCGTAGACATATGTTTATGCTGCCGACTTAAAACTTAAAATCATGAAGACAAAAATATCAAACTGGCTTATTAGATTAGCAGAAAAAATCAATCCACAAGAAAGATTGAGTAGTATTGAACGAGTTGATAACTACGAAGCGAAGAAGCTTGGTATCTGCCTTGTCCGGACTAAAAAAGAAATCAAGGATTACCGGAAAAAGAAGAAACTTGATGAAGGTTGGTCTAATCGAAAATCAGATGAAATGTTCCTCAAGGAAGTTAAGGATGAAGTTCGCCAATCAATTATCAGTTCGATCAACCAAAGGGGACTAATAGAATACTCCGTTGAAAAAGTTGGTGATGAACTCTATGTTACTGGTGAAATTAAAGTATATATAAAAAAAGAATAATATGCAGGTTCCTATAGATAACATAACTTTTAGCGAAAGTGAATATCATCGTGGAGACAAGATATGGAAAGCTCAAACACTCTACGATTTTGCTAAGGCAAAAGAATATCCAGTGCTTGATATGCCATTATGGAATATAGACCTTACAGCTGAACCATTTGAATGTAATCAGCTTCACAGTTTCATTTTTCAATGCAAACGGGTGAATCAATGCTCTCTTGAATATCCTATTATCCTTGACGAAGTAGGTCAAATTGCCGATGGCTACCATCGTTTATGTAAAGCGATATTGGAGGGCAAGGAGACAATTAAAGCTATCCGATTATTGGAGATGCCAGCACCTGATAGAATTTCGGAGGAATAAAAAAGCAAATGAACTAATGGCAAAACCCAAGATTCCAAATCAGAAAAAAAAGTACCAAGAACTCAACGGGAGATTAAACGGATATGTATCCCTCGTTGAGCAAATATACGATACCCTGAATTTGGAAGCTGCCAAATCTGTTTCACGTACTAAATATTCCCCTGATAGCGATAAGCCGTTTAAATGGTCTGACTATCCTCAAACGAAGAAACAGATAGATGACATACAGGCTCAATTTGTTGATGACATTCATGCCGCTATCTATCGTGGCACATCTGAAGAATGGAAGAACAGTAATGAAGCACAGGATTTAATAGCCAACAAAGTATTAAGAGCTTATAACGCCCAAGTTGACAAAGAGAAATATAAAGTTTTGTATCAAACAAATTCAGATGCTTTGAAAGCATTCCAGAACCGAAAAGATAAAGGATTAAATATATCTGCAAAACTTTGGCAACAATCTATGATCTACAAAGAAGAACTGGAGGCCGCGATCTCATGCGCTATTCAAAAAGGAACCAGTGCTGTTACGTTGAGTAAGCAAATAAGTAAGTATCTTCTTGATTTCCCATTACTGCAAAAAGATTACAAAGACAGATATGGCAGTGCTGAACATATACAAGATTGTGAATATCGTTCCATACGTCTAGCCCGTTCAGAAATAAATATGGCTTATAGAACAGCTGAAAACGAAAGATGGAAACAAATGGATTTCGTAGTCGGATATGAAATAAAACTAAGTTCTTCTCATCATAGCCGTATGCCACATGGAGACATTTGTGATACACTTGCCGGTAAATATCCTAAAGACTTCACATGGACAGGATGGCATCCGAATGATTTATGTTATAAAGTTCCTATCCTCAAAACAGAAGAAGAATTCTGGGAATGGGATGGGCGGATCGATGTTTCTACAGAAAGTATAAATGAAGTAAAGGATGTTCCTGACGAATTCAAAAAATGGGTACTCGAAAACCAACAAAAGATAGAAAAAGCCCGGAAAAGAAACACCTTACCTTATTTTTTGAGAGATAACAAATCAATTATTCAGAATATAAATACCGATAATTCAGCTAAGGAGCTTGTTAATCGTGCTTCTTTAGTTGGTAATGAGGTACAAAGTTTAGCGGAATCCATAGCTAAAAAGCACAAAGGATTTGTAACTCCAATCAATTACAAAAGTATTTCATCAATAACAAGAAAGGTGACAACGGAGAGTATAACTCCATATGATATAAAAGACGCTGTTAGGACGACAATTATAGTTCCTAAATCACAAATAGATCAAGTCTTGAACGAACTGTCTGAAAGCGATTCATTTGTTCGACTGAAAAGACAAAAACCGGAATCGTTTATGGGATATAGTGGGAATATAGTTAATATCCAAGCGTCTAACGGATTAATTGCCGAGATTCAAGTCAATACAGATCGTATGATTTATGCCAAAGAAAAGCCGGAAGACGCAAAACGAATTCTTGGAGAAAAACGTTGGAAAGAAATACAAAAGCAAACAGGTATGAAAGGGGGACTAGGACATAAATATTATGAAGAATGGCGAGTATTAGACAAGGCTGATAAAAAGGCGCAAAAAATAGCTGAAAAATCAATCGAATATTATAGTCATTTCCAATAAAAATCACTATCTTTACATATAAAAATGAACCAACAGGAATTATATAATAAATTACAGTCAGGCGAAACGGTTTATTTACTTGACGATTTTGAAGAAGCTGTTGTCCGTTTATATCTCGATAACGGTCAAACAAAATCATATATAAAACATCGTGGGTGTAACGAGATAGGAATTCCTCAATCCAATGAGACAGTTTGTGATATAATTCTTGGAGGAAAAGAAATTTCAAAATCAGAATATGACAAATACTAGTACTTTATTAGAAAAAGCTCTTCAAATCGCCGTCAAAGCCCATAGCGGACAAATCGATAAAGCTGGATCAGCCTACATCTTCCATCCTATCCGTGTCTCAAACAGATGTTCTACTGATGACGAAAGGATTGTCGCTTTACTGCACGATACAATAGAAGATACCGAAGTTACCGCTGAATATTTACTTATGGAAGGGTTTCCTCGTAATATAGTAGATGCTATACTTTCTGTCACTCGCAACGAGGATGAAAGCTATGACGATTTCATAAAACGTTCTAGACTTAATCCTATAGGAAGACAAGTAAAACTACATGATTTAGAAGACAACATGGATATAACACGTTTGAATGAACTTACAGAAAAGGATATTTACAGATTAAACAAATACATAAAAGCATATAAATATCTTAAAGAATAA

Protein sequences of DBSCAN-SWA_2

>NZ_CP022412|2710220:2718149|2715483_2715846_+|WP_005676525.1|DBSCAN-SWA
MQVPIDNITFSESEYHRGDKIWKAQTLYDFAKAKEYPVLDMPLWNIDLTAEPFECNQLHSFIFQCKRVNQCSLEYPIILDEVGQIADGYHRLCKAILEGKETIKAIRLLEMPAPDRISEE
>NZ_CP022412|2710220:2718149|2714768_2715059_+|WP_005676527.1|DBSCAN-SWA
MAKIDVLEFSKEKQGYSCEFTSVGKCVIQIDREMNGTLSLFAKLEGMDYALLYQYPSAQFNDNVIFELDVQKGLSIKILSTVGVMSAKMAYEDEDL
>NZ_CP022412|2710220:2718149|2713348_2714749_+|WP_005676528.1|portal|DBSCAN-SWA
MDEITSILDSTRPVDNIINDLKEKSVTVPSWDKLLKDYEPTEHEIVSDTVTRKDKIRSNGDIEKASRIYIGLEKLLTKRMTEFMFAIPVKRVYHNIEDNETRQSIAKAIEAIYKYSRIDSENIKRGNAYFASCEVFTIWYTVESFNTLYGFKSKYKLKCKTYSPMDGVRLYPLLDELGDMIAMSFEYTKKVKNVEVTYFETYTANIHYKWEQQGNGWELVKSEPVVILKIPGVYVYRPVPIYHGLSYIRKEIEYTLSRNSDVIAYNSAPILKIAGGIKGGEDKGESRRVYRVEQNGDVSYVSWAQSIEALKYHVDTLIKLFWSQSQMPDISFENMKSLGNIGFDARQTLLTDAHLKVGDESGAWIEAFERECSVIKAFLKMMNVSWKDEVDNVEVEHIITPFIQNDEKSEIEKWVTASGGKAVVSQLEAIKNLGISTDPQDTLSQIQKEDAEASKSRISNIFEQSE
>NZ_CP022412|2710220:2718149|2715862_2717479_+|WP_005676523.1|DBSCAN-SWA
MAKPKIPNQKKKYQELNGRLNGYVSLVEQIYDTLNLEAAKSVSRTKYSPDSDKPFKWSDYPQTKKQIDDIQAQFVDDIHAAIYRGTSEEWKNSNEAQDLIANKVLRAYNAQVDKEKYKVLYQTNSDALKAFQNRKDKGLNISAKLWQQSMIYKEELEAAISCAIQKGTSAVTLSKQISKYLLDFPLLQKDYKDRYGSAEHIQDCEYRSIRLARSEINMAYRTAENERWKQMDFVVGYEIKLSSSHHSRMPHGDICDTLAGKYPKDFTWTGWHPNDLCYKVPILKTEEEFWEWDGRIDVSTESINEVKDVPDEFKKWVLENQQKIEKARKRNTLPYFLRDNKSIIQNINTDNSAKELVNRASLVGNEVQSLAESIAKKHKGFVTPINYKSISSITRKVTTESITPYDIKDAVRTTIIVPKSQIDQVLNELSESDSFVRLKRQKPESFMGYSGNIVNIQASNGLIAEIQVNTDRMIYAKEKPEDAKRILGEKRWKEIQKQTGMKGGLGHKYYEEWRVLDKADKKAQKIAEKSIEYYSHFQ
>NZ_CP022412|2710220:2718149|2717717_2718149_+|WP_005676521.1|DBSCAN-SWA
MTNTSTLLEKALQIAVKAHSGQIDKAGSAYIFHPIRVSNRCSTDDERIVALLHDTIEDTEVTAEYLLMEGFPRNIVDAILSVTRNEDESYDDFIKRSRLNPIGRQVKLHDLEDNMDITRLNELTEKDIYRLNKYIKAYKYLKE
>NZ_CP022412|2710220:2718149|2717503_2717731_+|WP_005676522.1|DBSCAN-SWA
MNQQELYNKLQSGETVYLLDDFEEAVVRLYLDNGQTKSYIKHRGCNEIGIPQSNETVCDIILGGKEISKSEYDKY
>NZ_CP022412|2710220:2718149|2710695_2712237_+|WP_005676533.1|DBSCAN-SWA
MVTKDEKKELISEIIAYWSNDWNKFVRDALCARLDREQQAIIESVQHNPMTAVASGTARGKDFVAACASLCFMYLTPRFNEKGVLVGNTKVAMTAPTGRQVKNIMTPEIRRLIRAARTKFPFCCPGRLVADDIRTDYEEWFLTGFKADDNATESWSGFHAANTMFVITEASGISEIVYNAIEGNLQGNSRMLIVFNPNITTGYAARAMKSDRFAKFRLSSLNAENVVKKQIVIPGQVDYEWVKDKVINWCSPIQQTDFNEGEGDFNWEGKLYRPNDLFRVKVLGMFPKVSEDVLIPYEWIEIANRNWQELQASGFIPAKSCKLGVDVAGMGRDNSVLCPRYGNYVPQFDVHQSAGRADHMHVVGMTIPYLKKKGAKAFIDTIGEGAGVYSRLLEEEFTNAFSCKYSEGTDGLHDITGEYEFANMRAYLYWALRDWLNPKNGFGAALPPCDQLMEEATETKWKFLSNGKVIIEPKEDVKKRIKRSPDYMDALANTFYPRNYSFISDEELLKDFL
>NZ_CP022412|2710220:2718149|2712477_2712660_+|WP_005676532.1|DBSCAN-SWA
MKATAIQQRIIEKFIMSEFAQGNLDTKEQVSCMLLLIQKKLDMSVEQASDFMRNAIGINA
>NZ_CP022412|2710220:2718149|2712997_2713270_+|WP_005676529.1|DBSCAN-SWA
MTQERLDIFEKVLFLYGEYVLLDLYSFAKVTERYEDCAIMRDLMKKYNIDERDDIQDWQAELWRCGYSGKIAVINFPYYMHKAIKLVGYL
>NZ_CP022412|2710220:2718149|2715134_2715482_+|WP_005676526.1|DBSCAN-SWA
MKTKISNWLIRLAEKINPQERLSSIERVDNYEAKKLGICLVRTKKEIKDYRKKKKLDEGWSNRKSDEMFLKEVKDEVRQSIISSINQRGLIEYSVEKVGDELYVTGEIKVYIKKE
>NZ_CP022412|2710220:2718149|2710220_2710712_+|WP_005676534.1|DBSCAN-SWA
MAGRGRPKLEMSLYDKYIKGKEDIIIADCRNGADNKGLCVRLGIGLTTFKSILKKHPEVVDLLREGKEEADMKVESALYKRAIGYDIEETTTEVRIGEDGSGQTTVVKKTKKHVAGDTTAQIFWLKNRRPNEWKDKQDVNVTNNDWVDALKSLTTSYKNGDKG
>NZ_CP022412|2710220:2718149|2712671_2712989_+|WP_005676531.1|DBSCAN-SWA
MKVYDINGNVVAEGYLVPNPNFIPKGEYKETELDYQKKQADMLITSIDGNFYEISLPKSATLRQKINKDIQGYGRNVRRYNENIIHVTEKVLKILQTKYTIMCDF

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_005676534.1|2710220_2710712_+	hypothetical protein	A0A0E3U2Q7	Fusobacterium_phage	2.0e-20	41.0
WP_005676533.1|2710695_2712237_+	hypothetical protein	A0A0A8WEW2	Clostridium_phage	2.1e-31	26.7
WP_005676532.1|2712477_2712660_+	hypothetical protein	NA	NA	NA	NA
WP_005676531.1|2712671_2712989_+	hypothetical protein	NA	NA	NA	NA
WP_005676529.1|2712997_2713270_+	hypothetical protein	NA	NA	NA	NA
WP_005676528.1|2713348_2714749_+|portal	phage portal protein	F5A3C6	Riemerella_phage	5.2e-45	32.6
WP_005676527.1|2714768_2715059_+	hypothetical protein	NA	NA	NA	NA
WP_005676526.1|2715134_2715482_+	hypothetical protein	NA	NA	NA	NA
WP_005676525.1|2715483_2715846_+	hypothetical protein	I6R9T2	Croceibacter_phage	2.5e-20	39.8
WP_005676523.1|2715862_2717479_+	hypothetical protein	F5A3C5	Riemerella_phage	5.8e-32	30.8
WP_005676522.1|2717503_2717731_+	hypothetical protein	NA	NA	NA	NA
WP_005676521.1|2717717_2718149_+	hypothetical protein	A0A141E1X8	Streptococcus_phage	1.1e-25	43.7