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_CP045293	Paenibacillus guangzhouensis strain KCTC 33171 chromosome, complete genome	10 crisprs	cas3,DEDDh,WYL,csa3,DinG	2	13	4	0
NZ_CP045294	Paenibacillus guangzhouensis strain KCTC 33171 plasmid unnamed1, complete sequence	0 crisprs	NA	0	0	1	0

1. NZ_CP045293

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP045293_2

• CRISPR_ID: NZ_CP045293_2
• CRISPR_location: 289354-289504
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045293_2

Consensus_repeat	Method
GAAATAAATTTCTTTTCAGGAGCTTGAGCGAAGACAGGTGGGGTAG	CRISPRCasFinder

spacers of NZ_CP045293_2

>2.1|289400|59|NZ_CP045293|CRISPRCasFinder
GAATCTCCTTCGATGCAACAGGTTCAAGGACTTTCTTGTCAATGTTTTGAGGTGACTTG

CRISPR arrays and Neighbor proteins around NZ_CP045293_2

CRISPR arrays

The CRISPR arrays of NZ_CP045293_2

>merge|NZ_CP045293|2|289354-289504|CRISPRCasFinder
GAAATAAATTTCTTTTCAGGAGCTTGAGCGAAGACAGGTGGGGTAGGAATCTCCTTCGATGCAACAGGTTCAAGGACTTTCTTGTCAATGTTTTGAGGTGACTTGGAAATAAATTTCTTTTCAGGAGCTTGAGCGAAGACTGGTGGGGTAG

>NZ_CP045293|2|2|289354-289504|CRISPRCasFinder
GAAATAAATTTCTTTTCAGGAGCTTGAGCGAAGACAGGTGGGGTAG	GAATCTCCTTCGATGCAACAGGTTCAAGGACTTTCTTGTCAATGTTTTGAGGTGACTTG
GAAATAAATTTCTTTTCAGGAGCTTGAGCGAAGACTGGTGGGGTAG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045293.1|WP_152391863.1|291136_292096_+|NTP-transferase-domain-containing-protein	unknown	unknown	gnl|CDD|133032
NZ_CP045293.1|WP_152391870.1|298157_298586_+|GerAB/ArcD/ProY-family-transporter	unknown	unknown	gnl|CDD|281794
NZ_CP045293.1|WP_152391855.1|282498_282954_+|NUDIX-domain-containing-protein	unknown	unknown	gnl|CDD|239519
NZ_CP045293.1|WP_152391866.1|294535_295144_+|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|225136
NZ_CP045293.1|WP_152391861.1|287793_288933_-|glycosyltransferase	unknown	unknown	gnl|CDD|340831
NZ_CP045293.1|WP_152391856.1|283003_283546_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|224584
NZ_CP045293.1|WP_152391854.1|281893_282457_+|YdcF-family-protein	unknown	unknown	gnl|CDD|99750
NZ_CP045293.1|WP_152391869.1|296961_297939_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP045293.1|WP_152391871.1|298582_299083_+|GerAB/ArcD/ProY-family-transporter	unknown	unknown	gnl|CDD|281794
NZ_CP045293.1|WP_152391860.1|285868_286645_-|sporulation-protein	unknown	unknown	gnl|CDD|369195
NZ_CP045293.1|WP_152391868.1|295894_296941_+|phosphotransferase	unknown	unknown	gnl|CDD|270702
NZ_CP045293.1|WP_152391858.1|284146_284755_+|hypothetical-protein	unknown	unknown	gnl|CDD|223489
NZ_CP045293.1|WP_152391865.1|293407_294355_+|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|187566
NZ_CP045293.1|WP_152391857.1|283623_284082_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152391867.1|295455_295722_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152391852.1|280669_281053_+|glyoxalase	unknown	unknown	gnl|CDD|319937
NZ_CP045293.1|WP_152391872.1|299079_299295_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152391864.1|292108_293401_+|nucleotide-sugar-dehydrogenase	unknown	unknown	gnl|CDD|223936
NZ_CP045293.1|WP_152391853.1|281290_281860_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP045293.1|WP_152391859.1|284735_285785_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045293.1|WP_152391863.1|291136_292096_+|NTP-transferase-domain-containing-protein	gnl|CDD|133032	cd04189, G1P_TT_long, G1P_TT_long represents the long form of glucose-1-phosphate thymidylyltransferase. This family is the long form of Glucose-1-phosphate thymidylyltransferase. Glucose-1-phosphate thymidylyltransferase catalyses the formation of dTDP-glucose, from dTTP and glucose 1-phosphate. It is the first enzyme in the biosynthesis of dTDP-L-rhamnose, a cell wall constituent and a feedback inhibitor of the enzyme.There are two forms of Glucose-1-phosphate thymidylyltransferase in bacteria and archeae; short form and long form. The long form, which has an extra 50 amino acids c-terminal, is found in many species for which it serves as a sugar-activating enzyme for antibiotic biosynthesis and or other, unknown pathways, and in which dTDP-L-rhamnose is not necessarily produced.The long from enzymes also have a left-handed parallel helix domain at the c-terminus, whereas, th eshort form enzymes do not have this domain. The homotetrameric, feedback inhibited short form is found in numerous bacterial species that produce dTDP-L-rhamnose.	3.82414e-110
NZ_CP045293.1|WP_152391870.1|298157_298586_+|GerAB/ArcD/ProY-family-transporter	gnl|CDD|281794	pfam03845, Spore_permease, Spore germination protein.	9.3761e-11
NZ_CP045293.1|WP_152391855.1|282498_282954_+|NUDIX-domain-containing-protein	gnl|CDD|239519	cd03427, MTH1, MutT homolog-1 (MTH1) is a member of the Nudix hydrolase superfamily. MTH1, the mammalian counterpart of MutT, hydrolyzes oxidized purine nucleoside triphosphates, such as 8-oxo-dGTP and 2-hydroxy-ATP, to monophosphates, thereby preventing the incorporation of such oxygen radicals during replication. This is an important step in the repair mechanism in genomic and mitochondrial DNA. Like other members of the Nudix family, it requires a divalent cation, such as Mg2+ or Mn2+, for activity, and contain the Nudix motif, a highly conserved 23-residue block (GX5EX7REUXEEXGU, where U = I, L or V), that functions as a metal binding and catalytic site. MTH1 is predominantly localized in the cytoplasm and mitochondria. Structurally, this enzyme adopts a similar fold to MutT despite low sequence similarity outside the conserved nudix motif. The most distinctive structural difference between MutT and MTH1 is the presence of a beta-hairpin, which is absent in MutT. This results in a much deeper and narrower substrate binding pocket. Mechanistically, MTH1 contains dual specificity for nucleotides that contain 2-OH-adenine bases and those that contain 8-oxo-guanine bases.	5.85972e-47
NZ_CP045293.1|WP_152391854.1|281893_282457_+|YdcF-family-protein	gnl|CDD|99750	cd06259, YdcF-like, YdcF-like. YdcF-like is a large family of mainly bacterial proteins, with a few members found in fungi, plants, and archaea. Escherichia coli YdcF has been shown to bind S-adenosyl-L-methionine (AdoMet), but a biochemical function has not been idenitified. The family also includes Escherichia coli sanA and Salmonella typhimurium sfiX, which are involved in vancomycin resistance; sfiX may also be involved in murein synthesis.	1.05171e-35
NZ_CP045293.1|WP_152391856.1|283003_283546_+|GNAT-family-N-acetyltransferase	gnl|CDD|224584	COG1670, RimL, Acetyltransferases, including N-acetylases of ribosomal proteins [Translation, ribosomal structure and biogenesis].	5.60847e-39
NZ_CP045293.1|WP_152391852.1|280669_281053_+|glyoxalase	gnl|CDD|319937	cd08349, BLMA_like, Bleomycin binding protein (BLMA) and similar proteins. BLMA also called Bleomycin resistance protein, confers Bm resistance by directly binding to Bm. Bm is a glycopeptide antibiotic produced naturally by actinomycetes. It is a potent anti-cancer drug, which acts as a strong DNA-cutting agent, thereby causing cell death. BLMA is produced by actinomycetes to protect themselves against their own lethal compound. BLMA has two identically-folded subdomains, with the same alpha/beta fold; these two halves have no sequence similarity. BLMAs are dimers and each dimer binds to two Bm molecules at the Bm-binding pockets formed at the dimer interface; two Bm molecules are bound per dimer. BLMA belongs to a conserved domain superfamily that is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. As for the larger superfamily, this family contains members with or without domain swapping.	0.000262927
NZ_CP045293.1|WP_152391871.1|298582_299083_+|GerAB/ArcD/ProY-family-transporter	gnl|CDD|281794	pfam03845, Spore_permease, Spore germination protein.	2.33787e-13
NZ_CP045293.1|WP_152391860.1|285868_286645_-|sporulation-protein	gnl|CDD|369195	pfam07070, Spo0M, SpoOM protein. This family consists of several bacterial SpoOM proteins which are thought to control sporulation in Bacillus subtilis.Spo0M exerts certain negative effects on sporulation and its gene expression is controlled by sigmaH.	3.61736e-102
NZ_CP045293.1|WP_152391866.1|294535_295144_+|methyltransferase-domain-containing-protein	gnl|CDD|225136	COG2226, UbiE, Methylase involved in ubiquinone/menaquinone biosynthesis [Coenzyme metabolism].	2.14507e-18
NZ_CP045293.1|WP_152391858.1|284146_284755_+|hypothetical-protein	gnl|CDD|223489	COG0412, COG0412, Dienelactone hydrolase and related enzymes [Secondary metabolites biosynthesis, transport, and catabolism].	5.64442e-23
NZ_CP045293.1|WP_152391865.1|293407_294355_+|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|187566	cd05256, UDP_AE_SDR_e, UDP-N-acetylglucosamine 4-epimerase, extended (e) SDRs. This subgroup contains UDP-N-acetylglucosamine 4-epimerase of Pseudomonas aeruginosa, WbpP, an extended SDR, that catalyzes the NAD+ dependent conversion of UDP-GlcNAc and UDPGalNA to UDP-Glc and UDP-Gal. This subgroup has the characteristic active site tetrad and NAD-binding motif of the extended SDRs. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	1.36126e-91
NZ_CP045293.1|WP_152391869.1|296961_297939_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	1.25947e-09
NZ_CP045293.1|WP_152391861.1|287793_288933_-|glycosyltransferase	gnl|CDD|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	1.95976e-58
NZ_CP045293.1|WP_152391868.1|295894_296941_+|phosphotransferase	gnl|CDD|270702	cd05153, HomoserineK_II, Type II Homoserine Kinase. This subfamily is composed of unusual homoserine kinases, from a subset of bacteria, which have a Protein Kinase fold. These proteins do not bear any similarity to the GHMP family homoserine kinases present in most bacteria and eukaryotes. Homoserine kinase catalyzes the transfer of the gamma-phosphoryl group from ATP to L-homoserine producing L-homoserine phosphate, an intermediate in the production of the amino acids threonine, methionine, and isoleucine. The Type II homoserine kinase subfamily is part of a larger superfamily that includes the catalytic domains of other kinases, such as the typical serine/threonine/tyrosine protein kinases (PKs), RIO kinases, actin-fragmin kinase (AFK), and phosphoinositide 3-kinase (PI3K).	1.65634e-32
NZ_CP045293.1|WP_152391853.1|281290_281860_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	8.94357e-15
NZ_CP045293.1|WP_152391864.1|292108_293401_+|nucleotide-sugar-dehydrogenase	gnl|CDD|223936	COG1004, Ugd, Predicted UDP-glucose 6-dehydrogenase [Cell envelope biogenesis, outer membrane].	0

Protein sequences

>NZ_CP045293.1|WP_152391861.1|287793_288933_-|glycosyltransferase
MNVLLICTEKLPVPNIRGGAIQTYIGGVTKQLSEHHQVTIIGKSDPTLLSDESVGGVRYVRVPSDGMFELYLEGVIHFISTSGQNYDLIHIFNRPRMVLPVRGVAANARIILSMHNDMFNPTKLTTEEGRAVIAHTETIITISNYIGQEIERYFPEAKPKLRTIYSAVDLDRFAPWIESNTARQSRQEIRDQYQLQSKKIILFVGRLSRNKGPHVLVRAMSHLRHPDACLVVVGGAWYSDHRVSDYIGYVRALAERSTLPVITTGYIDAHDIHRWFCAADVFVCTSIWDEPLARVHYEAMAAGLPFITTARGGNPEIIINDNGLLISNPEDPLEYAEKLNNMLSNMENSRKMGLRGRRLTEQRFHWQRVAQDILSVWGT
>NZ_CP045293.1|WP_152391860.1|285868_286645_-|sporulation-protein
MSFFNKMLAKVGIGAAEVDTLLEEVSYVPGEDVRGVVRVTGGQVDQEIDRIYLQLMTRYVRESGDNKVTEHYSLAKFNVSGKMTIRGGETMEIPFSFPLPLETPVTYNGQPVWLHTGLDIDVAIDPTDNDGIEVRPHPYMDVIFQAVQSLGFRFRSSSCEYHSRLGRGVPFVQEFEFLPGSSFANRVKELELIMKVDHNGVNVLIEIDRKARGLTGLFEQALDMDERLVRVYFTETELDQGPQVIAQELAAIIQQQAR
>NZ_CP045293.1|WP_152391859.1|284735_285785_+|hypothetical-protein
MGSIHHKAVLDNYHFSGLEASQIGALLSALRYYNVPVTASWIYGMTGMAFLLVHDHDFKKPNAGPPEPQIFKLARNLGLEIEGIHTYAENESFRTLQQEMWQHAQTAIHKGYPVFAKNLDIRNQTSLVYGVDAEGYYTHSWHCGEGHENWDDVIPWHRLGQAYCPCRYCLTRRETSGYIEEERGLISLHAAKFIQPAEPLAALRDALHFVLSLNQQGVLHWQHHTYYIGEQAYEGWIQALERDEITKYEFSLTIEPLADARKHAVSFISEWRDLGLGLSSELLDAAVEKYAKIAASYQRLVQKYPYEQPSEFMTATERLACVDILRSLLHDEKQALDILVLLYEQIQAR
>NZ_CP045293.1|WP_152391858.1|284146_284755_+|hypothetical-protein
MNKPNNTLVILLHEIYGVNDHMQYYRDQWLQEGVDVLTPDLLHGRVFSYAQDEQAYQYFVNEIGFEQAAEEVRKIILTHRANYDRIFLMGFSIGATLAWMNSASGVDGMIGFYGSRIRNYADLVPGCQALLFFASQEKSFDVSALADQLHGKTNTITEVIQGEHGFMNPFHHAYLPDESKQCMMKSMNYILEEVAAIGVNPS
>NZ_CP045293.1|WP_152391857.1|283623_284082_+|hypothetical-protein
MERVKFRDSKRSKAIADLAKQTDHRLLARWATDCAEHVLSLFEAHCPGDNRPREAIEAGRAWVRGEIPMVEARAAAFASHTAARDIEHPAACAAARAAGHASATAHVAGHAVHAATYAAKAAAYAADDPSETSSSIAKERDWQYQRLLDLQQ
>NZ_CP045293.1|WP_152391856.1|283003_283546_+|GNAT-family-N-acetyltransferase
MDFPILETRRLKLRQLRLDDAPDLYDYFSQDKVTTYYDLDRFTELKQAEDLIQMWIDNFDSQRSIRWGITLKSEDRVIGTCGFHKWSQKHHRAEIGYELSPAYWRQGYMGEVVDAVVRYGFHGFDLHRIEAQIFQANIGSRKVLEKIGFQEEGVLQDYFYLKDQYVDAVIFAMCKSGKWA
>NZ_CP045293.1|WP_152391855.1|282498_282954_+|NUDIX-domain-containing-protein
MSNVEMTNMCMIYDPETNKVLVQERIKSWKGIAFPGGHIEDGESIIDSTIREIHEETGLTISNLELCGIVYWYNDATGDKYLVFSYRTQVFSGQLLDETEEGRLFWVDKDELASLPLAEGLKERLPLFLENQYSEGFGIWNEHRKTEMKWQ
>NZ_CP045293.1|WP_152391854.1|281893_282457_+|YdcF-family-protein
MYPFDCITDFMFFETRIEPADLILIPGGSHPQLMERAAELYHQGLAPYLLPSGGATAHVTTTEWAFLRDVGLQLGVPEQAILREDQARNTFDNARFSWQVIQEHGLQPKKVILVCKSYHARRALLTYQTVFPMDVTICVSPVTDKTGITKENWFLEDSTIRIVMNELTKVGRYFAHHIPNWVNSKRE
>NZ_CP045293.1|WP_152391853.1|281290_281860_+|GNAT-family-N-acetyltransferase
MQPIHYFTEIKSLVQVTAEEILSLGDFGYISNQKYEVKKEESLQSCAIMLQLVDLDEPYVKQDLIEADDLNRYQDLIKQGYSLGLYVDHKLIALAIAEAQTWNNTLLLWYLHVHEDHRRQRYGHALLSKMIELAQGSGFRALTLEAQNTNVPAIHFYKSLGFEIEGIDLSLYNLGEDNEEVALFLRKKF
>NZ_CP045293.1|WP_152391852.1|280669_281053_+|glyoxalase
MGKGFSHCLQIFPTPDLHKTTAYYETLGFRAVYYLESSEPHVCLYRDAIEIVLTKSKQETIVPNRVMHGYGYDGYFIAEKQRELEQEFMHLGINIVRSLGTTDYNNREFVFDDVDGRWIAVGNKNGT
>NZ_CP045293.1|WP_152391863.1|291136_292096_+|NTP-transferase-domain-containing-protein
MKGLIVCAGRGTRLQPFSYLTSKVLLPVANKPLIFYSLEKLKSLGITEIGIVIQPAQKLLFEEQVGDGIDRGVHITYLFQEMPLGIADAVKQSETFIGSDSFILLLGDNLISQSLSVLKDSILVDHYDGALLLGKVENPHEYGIAEIEEQRIIGLEEKPLQPKSNLAIVGAYAFTAQIFKAIDAITPSRRGEYEITDAIQYLIQHGYSISYDITTSPHTDVGTPGRWLEANRWMLQTMPVEKTTTMNESYEGSILKSPVLIDPSSTLLNCDIGPYVVIGPGVVLENCKIEDSIILEGVNLRNRTLKGSIVSIHHAVPPI
>NZ_CP045293.1|WP_152391864.1|292108_293401_+|nucleotide-sugar-dehydrogenase
MNILVVGVGYVGTTTALLFAELGYKITGFDTDIHKIQALKEGNLPFFEPGLDTLLNKHVQQGSLSFTTDPVQAIREHQVIFICVGTPSQADGSTDLTYVQNVSETIGSYMESYKLIVIKSTVPIGTHKKVSEWVTDAQHEHLPFDVVMNPEFLREGNAVYDCFHPERIVIGSDSAIAAGQVSLLYHSIDCPLVMTNPATAEMIKYASNAFLATKISYMNELARLCDQVDVSISTVAQGMGLDSRISRSFLKAGIGYGGSCFPKDVFSLLHTAKDYGIDLNLIRSVVEVNNTQCQYFMKRIRRKLGILRGKRIAILGLSFKPGTDDMREAPAFTMMKGLLECGSYLKVHDPVAKLPDGWKTHAIKQYDSVEETLRSAHAVILCTEWSEYVEGDWDAWRQLLKFPYLFDGRNVLDRSQLESRGWDYNGIGNG
>NZ_CP045293.1|WP_152391865.1|293407_294355_+|NAD-dependent-epimerase/dehydratase-family-protein
MSRILVTGAAGFIGSHLCEELLLDESNQVIGIDAFIDFTTPTWMRRRNIGSLLDHLRFEWVDSNLLTVSWDELLTRVDIIYHLAGMPGVRSSWGPDFVQYATHNIVATQRLLEACKRYPLQRFIFASTSSVYGEKTGRVDEQATMLPLSPYGISKLTCEHLCRVYGDAGIPVVVLRFFTVYGPRQRPDMAFHRFIKQMLDRQPITLYGDGTQSRDFTYVLDCVRAVAAVAHANGVVGETINIGGKERASINECIALLEELFEQKAQIEVVRNTFGEPTSTWADVSKAEKLLGYSPTVDLKTGLSMEIQYLRELYQ
>NZ_CP045293.1|WP_152391866.1|294535_295144_+|methyltransferase-domain-containing-protein
MDKDKLIHKFDRQAGVYDRRRQKSSDRTWREPLVSCAYGKVLEISVGAGANFPFYPKDVEVTAVDFSNEMLLAAQRGAADHRLQVTFLQSDVESLAFPANTFDTIVSTLSFCGYENPLQVLASLKEWCKPNGQILLMEHGRSSSPIIRPLQHIINPMFRRMVGCHVNRDIMGMVQQAGLHIEREEHHWLDMIHRVWARPNKS
>NZ_CP045293.1|WP_152391867.1|295455_295722_+|hypothetical-protein
MKYINADVVLPDHLLKELQQYVPGGMLYVPKPAGLRKKWGEKSGSRLYLSRRNDEIRQKFSVGTSIDQLSDQFCLSYDSIKKIVYSKK
>NZ_CP045293.1|WP_152391868.1|295894_296941_+|phosphotransferase
MQDFFQMDTEEKRTNLLARARQAALSAMEQYDLTSEQMTFIQLSDSITYQIETSSGETYLLRIHADQWKKEELRSELLLLQYLSHDAGMTVPTGVASRDGSCILEVAAEEGYRNPCVTLMRWVEGEGLNEMQDEDAYELGVMAGNLHAAVAQFNPPGHFVRPSLGIESFREEVARLAQYYDRFLSESAWEMYQLAANQILASLAEMTRTNDNYGLIHGDLHTGNIMFHEGTPYPIDFGRCSYGYYLYDVASTILGLVPKQRAMFMQGYLKVRSLTEEDLQHLETFFVMVLIGNYSHHAANPAERSNLIDEQPYAQAIIRAFLRVEPFLFQVIKPVEIECGSVPKTIIQ
>NZ_CP045293.1|WP_152391869.1|296961_297939_+|GNAT-family-N-acetyltransferase
MEIVIRRMVVPDDYEDVARLINVIASEVVTAQDLADEDARIPAVGSLSRDEEGRLTGHDRPRWIAKDGEGRTIGYAHAWRAPWSSPGVLYEQVIVDPNARHQGVGRALFDVVMAYTSEVRADRVIVDLRDDDPVSLAFATKRGFKQERHLFESCIELANLDRESLDYPAFANDSFQMMSLADRPGEAMEQQLYELYRATHEDIPGFEGEYMWYSEWRKWTLDKEDFERSLALLVLDGDRPIGVVQLTANPESESLYNSFTGVDAAYRGQGIARALKIQSIREAIKRGYRYIRTNNDSLNAPMLRINRSLGYQPVPGYYMMTRNIE
>NZ_CP045293.1|WP_152391870.1|298157_298586_+|GerAB/ArcD/ProY-family-transporter
MCKRFRTGSALVFPLNLDAKEAGWISKLLGMAAALIFYAVFCYIARDKPRQPFTVVIEGIIGKVPGKILASLYTLFFIYQASRQFNDFALLMSVSVFDQTPIIMIHAMMVVAIGYVLALGIVVLARTGEIFYVVMMSMIVLS
>NZ_CP045293.1|WP_152391871.1|298582_299083_+|GerAB/ArcD/ProY-family-transporter
MTPFLKEHGSLLRTGIISLIFSGLILAWITALNVSVLGVDILRQSFFPFLMSIGEVNISNFIQRLDVIAVMMLIIGVFFKASIFYAASAVAVYRLFHMTSFRKAILLVGTIIFLSALVISPNSSHHLQEGLISDQWIIYLPFEITIPVLLGGWVWLRNKFNRERST
>NZ_CP045293.1|WP_152391872.1|299079_299295_-|hypothetical-protein
MKNIAIFTALLAGSLLFDLVLDMPLGVSMYDDVQMILRKIQIIHPIILWLFGLTLVIILYVLGTNKKRTKS

Crispr_ID: NZ_CP045293_1

• CRISPR_ID: NZ_CP045293_1
• CRISPR_location: 286778-286980
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 4 spacers

Consensus repeat of NZ_CP045293_1

Consensus_repeat	Method
TCATCTTCCGAATCTTCTTCATC	CRISPRCasFinder

spacers of NZ_CP045293_1

>1.1|286801|16|NZ_CP045293|CRISPRCasFinder
CTTTGTTTACTGATCT
>1.2|286840|25|NZ_CP045293|CRISPRCasFinder
ATAACCATCTTCGTCGTCTTCGGAA
>1.3|286888|22|NZ_CP045293|CRISPRCasFinder
AACTTCTTCTGCTTCAACTTCT
>1.4|286933|25|NZ_CP045293|CRISPRCasFinder
CGAATCTTCTTCATCTTCTTCATCA

CRISPR arrays and Neighbor proteins around NZ_CP045293_1

CRISPR arrays

The CRISPR arrays of NZ_CP045293_1

>merge|NZ_CP045293|1|286778-286980|CRISPRCasFinder
CCAGCGGCTGAATCCTCTTAATCCTTTGTTTACTGATCTTCATCTTCTTCATACTCGTCATCATAACCATCTTCGTCGTCTTCGGAATCTTCTTCTTCATCAACTTCTTCAACTTCTTCTGCTTCAACTTCTTCTTCTTCTAAATTTTCATCTTCCGAATCTTCTTCATCTTCTTCATCATCGTCTTCCGAATCTTCTTCATC

>NZ_CP045293|1|1|286778-286980|CRISPRCasFinder
CCAGCGGCTGAATCCTCTTAATC	CTTTGTTTACTGATCT
TCATCTTCTTCATACTCGTCATC	ATAACCATCTTCGTCGTCTTCGGAA
TCTTCTTCTTCATCAACTTCTTC	AACTTCTTCTGCTTCAACTTCT
TCTTCTTCTAAATTTTCATCTTC	CGAATCTTCTTCATCTTCTTCATCA
TCGTCTTCCGAATCTTCTTCATC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045293.1|WP_152391851.1|280119_280539_+|metallothiol-transferase-FosB	unknown	unknown	gnl|CDD|179740
NZ_CP045293.1|WP_152391870.1|298157_298586_+|GerAB/ArcD/ProY-family-transporter	unknown	unknown	gnl|CDD|281794
NZ_CP045293.1|WP_152391855.1|282498_282954_+|NUDIX-domain-containing-protein	unknown	unknown	gnl|CDD|239519
NZ_CP045293.1|WP_152391854.1|281893_282457_+|YdcF-family-protein	unknown	unknown	gnl|CDD|99750
NZ_CP045293.1|WP_152391856.1|283003_283546_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|224584
NZ_CP045293.1|WP_152391861.1|287793_288933_-|glycosyltransferase	unknown	unknown	gnl|CDD|340831
NZ_CP045293.1|WP_152391869.1|296961_297939_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP045293.1|WP_152391868.1|295894_296941_+|phosphotransferase	unknown	unknown	gnl|CDD|270702
NZ_CP045293.1|WP_152391864.1|292108_293401_+|nucleotide-sugar-dehydrogenase	unknown	unknown	gnl|CDD|223936
NZ_CP045293.1|WP_152391860.1|285868_286645_-|sporulation-protein	unknown	unknown	gnl|CDD|369195
NZ_CP045293.1|WP_152391862.1|289037_290849_-|CotS-family-spore-coat-protein	unknown	unknown	gnl|CDD|131952
NZ_CP045293.1|WP_152391866.1|294535_295144_+|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|225136
NZ_CP045293.1|WP_152391858.1|284146_284755_+|hypothetical-protein	unknown	unknown	gnl|CDD|223489
NZ_CP045293.1|WP_152391865.1|293407_294355_+|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|187566
NZ_CP045293.1|WP_152391857.1|283623_284082_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152391867.1|295455_295722_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152391852.1|280669_281053_+|glyoxalase	unknown	unknown	gnl|CDD|319937
NZ_CP045293.1|WP_152391863.1|291136_292096_+|NTP-transferase-domain-containing-protein	unknown	unknown	gnl|CDD|133032
NZ_CP045293.1|WP_152391853.1|281290_281860_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP045293.1|WP_152391859.1|284735_285785_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045293.1|WP_152391851.1|280119_280539_+|metallothiol-transferase-FosB	gnl|CDD|179740	PRK04101, PRK04101, metallothiol transferase FosB.	8.65996e-88
NZ_CP045293.1|WP_152391870.1|298157_298586_+|GerAB/ArcD/ProY-family-transporter	gnl|CDD|281794	pfam03845, Spore_permease, Spore germination protein.	9.3761e-11
NZ_CP045293.1|WP_152391855.1|282498_282954_+|NUDIX-domain-containing-protein	gnl|CDD|239519	cd03427, MTH1, MutT homolog-1 (MTH1) is a member of the Nudix hydrolase superfamily. MTH1, the mammalian counterpart of MutT, hydrolyzes oxidized purine nucleoside triphosphates, such as 8-oxo-dGTP and 2-hydroxy-ATP, to monophosphates, thereby preventing the incorporation of such oxygen radicals during replication. This is an important step in the repair mechanism in genomic and mitochondrial DNA. Like other members of the Nudix family, it requires a divalent cation, such as Mg2+ or Mn2+, for activity, and contain the Nudix motif, a highly conserved 23-residue block (GX5EX7REUXEEXGU, where U = I, L or V), that functions as a metal binding and catalytic site. MTH1 is predominantly localized in the cytoplasm and mitochondria. Structurally, this enzyme adopts a similar fold to MutT despite low sequence similarity outside the conserved nudix motif. The most distinctive structural difference between MutT and MTH1 is the presence of a beta-hairpin, which is absent in MutT. This results in a much deeper and narrower substrate binding pocket. Mechanistically, MTH1 contains dual specificity for nucleotides that contain 2-OH-adenine bases and those that contain 8-oxo-guanine bases.	5.85972e-47
NZ_CP045293.1|WP_152391854.1|281893_282457_+|YdcF-family-protein	gnl|CDD|99750	cd06259, YdcF-like, YdcF-like. YdcF-like is a large family of mainly bacterial proteins, with a few members found in fungi, plants, and archaea. Escherichia coli YdcF has been shown to bind S-adenosyl-L-methionine (AdoMet), but a biochemical function has not been idenitified. The family also includes Escherichia coli sanA and Salmonella typhimurium sfiX, which are involved in vancomycin resistance; sfiX may also be involved in murein synthesis.	1.05171e-35
NZ_CP045293.1|WP_152391856.1|283003_283546_+|GNAT-family-N-acetyltransferase	gnl|CDD|224584	COG1670, RimL, Acetyltransferases, including N-acetylases of ribosomal proteins [Translation, ribosomal structure and biogenesis].	5.60847e-39
NZ_CP045293.1|WP_152391861.1|287793_288933_-|glycosyltransferase	gnl|CDD|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	1.95976e-58
NZ_CP045293.1|WP_152391868.1|295894_296941_+|phosphotransferase	gnl|CDD|270702	cd05153, HomoserineK_II, Type II Homoserine Kinase. This subfamily is composed of unusual homoserine kinases, from a subset of bacteria, which have a Protein Kinase fold. These proteins do not bear any similarity to the GHMP family homoserine kinases present in most bacteria and eukaryotes. Homoserine kinase catalyzes the transfer of the gamma-phosphoryl group from ATP to L-homoserine producing L-homoserine phosphate, an intermediate in the production of the amino acids threonine, methionine, and isoleucine. The Type II homoserine kinase subfamily is part of a larger superfamily that includes the catalytic domains of other kinases, such as the typical serine/threonine/tyrosine protein kinases (PKs), RIO kinases, actin-fragmin kinase (AFK), and phosphoinositide 3-kinase (PI3K).	1.65634e-32
NZ_CP045293.1|WP_152391860.1|285868_286645_-|sporulation-protein	gnl|CDD|369195	pfam07070, Spo0M, SpoOM protein. This family consists of several bacterial SpoOM proteins which are thought to control sporulation in Bacillus subtilis.Spo0M exerts certain negative effects on sporulation and its gene expression is controlled by sigmaH.	3.61736e-102
NZ_CP045293.1|WP_152391862.1|289037_290849_-|CotS-family-spore-coat-protein	gnl|CDD|131952	TIGR02906, Spore_coat_protein_S, spore coat protein, CotS family. Members of this family include the spore coat proteins CotS and YtaA from Bacillus subtilis and, from other endospore-forming bacteria, homologs that are more closely related to these two than to the spore coat proteins YutH and YsxE. The CotS family is more broadly distributed than YutH or YsxE, but still is not universal among spore-formers. [Cellular processes, Sporulation and germination].	4.68201e-94
NZ_CP045293.1|WP_152391866.1|294535_295144_+|methyltransferase-domain-containing-protein	gnl|CDD|225136	COG2226, UbiE, Methylase involved in ubiquinone/menaquinone biosynthesis [Coenzyme metabolism].	2.14507e-18
NZ_CP045293.1|WP_152391858.1|284146_284755_+|hypothetical-protein	gnl|CDD|223489	COG0412, COG0412, Dienelactone hydrolase and related enzymes [Secondary metabolites biosynthesis, transport, and catabolism].	5.64442e-23
NZ_CP045293.1|WP_152391865.1|293407_294355_+|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|187566	cd05256, UDP_AE_SDR_e, UDP-N-acetylglucosamine 4-epimerase, extended (e) SDRs. This subgroup contains UDP-N-acetylglucosamine 4-epimerase of Pseudomonas aeruginosa, WbpP, an extended SDR, that catalyzes the NAD+ dependent conversion of UDP-GlcNAc and UDPGalNA to UDP-Glc and UDP-Gal. This subgroup has the characteristic active site tetrad and NAD-binding motif of the extended SDRs. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	1.36126e-91
NZ_CP045293.1|WP_152391869.1|296961_297939_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	1.25947e-09
NZ_CP045293.1|WP_152391852.1|280669_281053_+|glyoxalase	gnl|CDD|319937	cd08349, BLMA_like, Bleomycin binding protein (BLMA) and similar proteins. BLMA also called Bleomycin resistance protein, confers Bm resistance by directly binding to Bm. Bm is a glycopeptide antibiotic produced naturally by actinomycetes. It is a potent anti-cancer drug, which acts as a strong DNA-cutting agent, thereby causing cell death. BLMA is produced by actinomycetes to protect themselves against their own lethal compound. BLMA has two identically-folded subdomains, with the same alpha/beta fold; these two halves have no sequence similarity. BLMAs are dimers and each dimer binds to two Bm molecules at the Bm-binding pockets formed at the dimer interface; two Bm molecules are bound per dimer. BLMA belongs to a conserved domain superfamily that is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. As for the larger superfamily, this family contains members with or without domain swapping.	0.000262927
NZ_CP045293.1|WP_152391863.1|291136_292096_+|NTP-transferase-domain-containing-protein	gnl|CDD|133032	cd04189, G1P_TT_long, G1P_TT_long represents the long form of glucose-1-phosphate thymidylyltransferase. This family is the long form of Glucose-1-phosphate thymidylyltransferase. Glucose-1-phosphate thymidylyltransferase catalyses the formation of dTDP-glucose, from dTTP and glucose 1-phosphate. It is the first enzyme in the biosynthesis of dTDP-L-rhamnose, a cell wall constituent and a feedback inhibitor of the enzyme.There are two forms of Glucose-1-phosphate thymidylyltransferase in bacteria and archeae; short form and long form. The long form, which has an extra 50 amino acids c-terminal, is found in many species for which it serves as a sugar-activating enzyme for antibiotic biosynthesis and or other, unknown pathways, and in which dTDP-L-rhamnose is not necessarily produced.The long from enzymes also have a left-handed parallel helix domain at the c-terminus, whereas, th eshort form enzymes do not have this domain. The homotetrameric, feedback inhibited short form is found in numerous bacterial species that produce dTDP-L-rhamnose.	3.82414e-110
NZ_CP045293.1|WP_152391853.1|281290_281860_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	8.94357e-15
NZ_CP045293.1|WP_152391864.1|292108_293401_+|nucleotide-sugar-dehydrogenase	gnl|CDD|223936	COG1004, Ugd, Predicted UDP-glucose 6-dehydrogenase [Cell envelope biogenesis, outer membrane].	0

Protein sequences

>NZ_CP045293.1|WP_152391860.1|285868_286645_-|sporulation-protein
MSFFNKMLAKVGIGAAEVDTLLEEVSYVPGEDVRGVVRVTGGQVDQEIDRIYLQLMTRYVRESGDNKVTEHYSLAKFNVSGKMTIRGGETMEIPFSFPLPLETPVTYNGQPVWLHTGLDIDVAIDPTDNDGIEVRPHPYMDVIFQAVQSLGFRFRSSSCEYHSRLGRGVPFVQEFEFLPGSSFANRVKELELIMKVDHNGVNVLIEIDRKARGLTGLFEQALDMDERLVRVYFTETELDQGPQVIAQELAAIIQQQAR
>NZ_CP045293.1|WP_152391859.1|284735_285785_+|hypothetical-protein
MGSIHHKAVLDNYHFSGLEASQIGALLSALRYYNVPVTASWIYGMTGMAFLLVHDHDFKKPNAGPPEPQIFKLARNLGLEIEGIHTYAENESFRTLQQEMWQHAQTAIHKGYPVFAKNLDIRNQTSLVYGVDAEGYYTHSWHCGEGHENWDDVIPWHRLGQAYCPCRYCLTRRETSGYIEEERGLISLHAAKFIQPAEPLAALRDALHFVLSLNQQGVLHWQHHTYYIGEQAYEGWIQALERDEITKYEFSLTIEPLADARKHAVSFISEWRDLGLGLSSELLDAAVEKYAKIAASYQRLVQKYPYEQPSEFMTATERLACVDILRSLLHDEKQALDILVLLYEQIQAR
>NZ_CP045293.1|WP_152391858.1|284146_284755_+|hypothetical-protein
MNKPNNTLVILLHEIYGVNDHMQYYRDQWLQEGVDVLTPDLLHGRVFSYAQDEQAYQYFVNEIGFEQAAEEVRKIILTHRANYDRIFLMGFSIGATLAWMNSASGVDGMIGFYGSRIRNYADLVPGCQALLFFASQEKSFDVSALADQLHGKTNTITEVIQGEHGFMNPFHHAYLPDESKQCMMKSMNYILEEVAAIGVNPS
>NZ_CP045293.1|WP_152391857.1|283623_284082_+|hypothetical-protein
MERVKFRDSKRSKAIADLAKQTDHRLLARWATDCAEHVLSLFEAHCPGDNRPREAIEAGRAWVRGEIPMVEARAAAFASHTAARDIEHPAACAAARAAGHASATAHVAGHAVHAATYAAKAAAYAADDPSETSSSIAKERDWQYQRLLDLQQ
>NZ_CP045293.1|WP_152391856.1|283003_283546_+|GNAT-family-N-acetyltransferase
MDFPILETRRLKLRQLRLDDAPDLYDYFSQDKVTTYYDLDRFTELKQAEDLIQMWIDNFDSQRSIRWGITLKSEDRVIGTCGFHKWSQKHHRAEIGYELSPAYWRQGYMGEVVDAVVRYGFHGFDLHRIEAQIFQANIGSRKVLEKIGFQEEGVLQDYFYLKDQYVDAVIFAMCKSGKWA
>NZ_CP045293.1|WP_152391855.1|282498_282954_+|NUDIX-domain-containing-protein
MSNVEMTNMCMIYDPETNKVLVQERIKSWKGIAFPGGHIEDGESIIDSTIREIHEETGLTISNLELCGIVYWYNDATGDKYLVFSYRTQVFSGQLLDETEEGRLFWVDKDELASLPLAEGLKERLPLFLENQYSEGFGIWNEHRKTEMKWQ
>NZ_CP045293.1|WP_152391854.1|281893_282457_+|YdcF-family-protein
MYPFDCITDFMFFETRIEPADLILIPGGSHPQLMERAAELYHQGLAPYLLPSGGATAHVTTTEWAFLRDVGLQLGVPEQAILREDQARNTFDNARFSWQVIQEHGLQPKKVILVCKSYHARRALLTYQTVFPMDVTICVSPVTDKTGITKENWFLEDSTIRIVMNELTKVGRYFAHHIPNWVNSKRE
>NZ_CP045293.1|WP_152391853.1|281290_281860_+|GNAT-family-N-acetyltransferase
MQPIHYFTEIKSLVQVTAEEILSLGDFGYISNQKYEVKKEESLQSCAIMLQLVDLDEPYVKQDLIEADDLNRYQDLIKQGYSLGLYVDHKLIALAIAEAQTWNNTLLLWYLHVHEDHRRQRYGHALLSKMIELAQGSGFRALTLEAQNTNVPAIHFYKSLGFEIEGIDLSLYNLGEDNEEVALFLRKKF
>NZ_CP045293.1|WP_152391852.1|280669_281053_+|glyoxalase
MGKGFSHCLQIFPTPDLHKTTAYYETLGFRAVYYLESSEPHVCLYRDAIEIVLTKSKQETIVPNRVMHGYGYDGYFIAEKQRELEQEFMHLGINIVRSLGTTDYNNREFVFDDVDGRWIAVGNKNGT
>NZ_CP045293.1|WP_152391851.1|280119_280539_+|metallothiol-transferase-FosB
MQIQGINHFCFSVSDLDQSIAFYERVFDAKLLVTGRTLAYFELNGLWIALNEEKDTPRPPLSTYTHIAFTVLEEEFDHWVDRLVQLNVHILPGRTRDERDRKSVYFTDPDGHKFEFHTGGLNDRLAYYRQDKKHMEFQD
>NZ_CP045293.1|WP_152391861.1|287793_288933_-|glycosyltransferase
MNVLLICTEKLPVPNIRGGAIQTYIGGVTKQLSEHHQVTIIGKSDPTLLSDESVGGVRYVRVPSDGMFELYLEGVIHFISTSGQNYDLIHIFNRPRMVLPVRGVAANARIILSMHNDMFNPTKLTTEEGRAVIAHTETIITISNYIGQEIERYFPEAKPKLRTIYSAVDLDRFAPWIESNTARQSRQEIRDQYQLQSKKIILFVGRLSRNKGPHVLVRAMSHLRHPDACLVVVGGAWYSDHRVSDYIGYVRALAERSTLPVITTGYIDAHDIHRWFCAADVFVCTSIWDEPLARVHYEAMAAGLPFITTARGGNPEIIINDNGLLISNPEDPLEYAEKLNNMLSNMENSRKMGLRGRRLTEQRFHWQRVAQDILSVWGT
>NZ_CP045293.1|WP_152391862.1|289037_290849_-|CotS-family-spore-coat-protein
MDQYQVVPWDHHVDVISTGTVLEQYVPPELEELAYQVMMNYDMYVSSMVLITSKPDKGGAIWRIDTDKGPRSLKVLHRLPQRSLFSVGAQQYLVEKGARVPALIPTKNNELYIEAGGKLWIVTDWIDTLQQASKIDLEGASALCLGLGEFHHHTKGYTSPPGAAKSSRLTGWTKYYQKIIAKIGWFRDIAQAYPDAAGSGPLLQVVDEFERQAKDALERLNQSSYAKMIAMGDAYWGLAHQDYGWSNGQMGPEGIWVIDLDGVAYDLPFRDLRKLMTSTMDDMGTWDITWIRSMIAAYHQGNPLTREMFEILSIDMAFPNEFYKHIKEVVFDTVNFLNVDLEPILQRVLATENTKWQVLEELWKDIDLYPAGNYVVEPVAIADLPIPPVLTKPSKPKMPTPTPASIPAPAPARAPGPAPILTPTPAATYNPPAAVDRKVVEPVASKEPSTPPVFAQAPEKKFISKSPQNIDKKVLEPVASKEIPTPPVFAQAPEKKFISKSPQNIDKKVLEPVTAAKDVPTPPQSKKVTKQKERKDYILPPNFASNTPKNVETAPEPTAPEPENNTPDSLEYSQQQTFYPVQRAHQEYREYLSERVPFYFRRR
>NZ_CP045293.1|WP_152391863.1|291136_292096_+|NTP-transferase-domain-containing-protein
MKGLIVCAGRGTRLQPFSYLTSKVLLPVANKPLIFYSLEKLKSLGITEIGIVIQPAQKLLFEEQVGDGIDRGVHITYLFQEMPLGIADAVKQSETFIGSDSFILLLGDNLISQSLSVLKDSILVDHYDGALLLGKVENPHEYGIAEIEEQRIIGLEEKPLQPKSNLAIVGAYAFTAQIFKAIDAITPSRRGEYEITDAIQYLIQHGYSISYDITTSPHTDVGTPGRWLEANRWMLQTMPVEKTTTMNESYEGSILKSPVLIDPSSTLLNCDIGPYVVIGPGVVLENCKIEDSIILEGVNLRNRTLKGSIVSIHHAVPPI
>NZ_CP045293.1|WP_152391864.1|292108_293401_+|nucleotide-sugar-dehydrogenase
MNILVVGVGYVGTTTALLFAELGYKITGFDTDIHKIQALKEGNLPFFEPGLDTLLNKHVQQGSLSFTTDPVQAIREHQVIFICVGTPSQADGSTDLTYVQNVSETIGSYMESYKLIVIKSTVPIGTHKKVSEWVTDAQHEHLPFDVVMNPEFLREGNAVYDCFHPERIVIGSDSAIAAGQVSLLYHSIDCPLVMTNPATAEMIKYASNAFLATKISYMNELARLCDQVDVSISTVAQGMGLDSRISRSFLKAGIGYGGSCFPKDVFSLLHTAKDYGIDLNLIRSVVEVNNTQCQYFMKRIRRKLGILRGKRIAILGLSFKPGTDDMREAPAFTMMKGLLECGSYLKVHDPVAKLPDGWKTHAIKQYDSVEETLRSAHAVILCTEWSEYVEGDWDAWRQLLKFPYLFDGRNVLDRSQLESRGWDYNGIGNG
>NZ_CP045293.1|WP_152391865.1|293407_294355_+|NAD-dependent-epimerase/dehydratase-family-protein
MSRILVTGAAGFIGSHLCEELLLDESNQVIGIDAFIDFTTPTWMRRRNIGSLLDHLRFEWVDSNLLTVSWDELLTRVDIIYHLAGMPGVRSSWGPDFVQYATHNIVATQRLLEACKRYPLQRFIFASTSSVYGEKTGRVDEQATMLPLSPYGISKLTCEHLCRVYGDAGIPVVVLRFFTVYGPRQRPDMAFHRFIKQMLDRQPITLYGDGTQSRDFTYVLDCVRAVAAVAHANGVVGETINIGGKERASINECIALLEELFEQKAQIEVVRNTFGEPTSTWADVSKAEKLLGYSPTVDLKTGLSMEIQYLRELYQ
>NZ_CP045293.1|WP_152391866.1|294535_295144_+|methyltransferase-domain-containing-protein
MDKDKLIHKFDRQAGVYDRRRQKSSDRTWREPLVSCAYGKVLEISVGAGANFPFYPKDVEVTAVDFSNEMLLAAQRGAADHRLQVTFLQSDVESLAFPANTFDTIVSTLSFCGYENPLQVLASLKEWCKPNGQILLMEHGRSSSPIIRPLQHIINPMFRRMVGCHVNRDIMGMVQQAGLHIEREEHHWLDMIHRVWARPNKS
>NZ_CP045293.1|WP_152391867.1|295455_295722_+|hypothetical-protein
MKYINADVVLPDHLLKELQQYVPGGMLYVPKPAGLRKKWGEKSGSRLYLSRRNDEIRQKFSVGTSIDQLSDQFCLSYDSIKKIVYSKK
>NZ_CP045293.1|WP_152391868.1|295894_296941_+|phosphotransferase
MQDFFQMDTEEKRTNLLARARQAALSAMEQYDLTSEQMTFIQLSDSITYQIETSSGETYLLRIHADQWKKEELRSELLLLQYLSHDAGMTVPTGVASRDGSCILEVAAEEGYRNPCVTLMRWVEGEGLNEMQDEDAYELGVMAGNLHAAVAQFNPPGHFVRPSLGIESFREEVARLAQYYDRFLSESAWEMYQLAANQILASLAEMTRTNDNYGLIHGDLHTGNIMFHEGTPYPIDFGRCSYGYYLYDVASTILGLVPKQRAMFMQGYLKVRSLTEEDLQHLETFFVMVLIGNYSHHAANPAERSNLIDEQPYAQAIIRAFLRVEPFLFQVIKPVEIECGSVPKTIIQ
>NZ_CP045293.1|WP_152391869.1|296961_297939_+|GNAT-family-N-acetyltransferase
MEIVIRRMVVPDDYEDVARLINVIASEVVTAQDLADEDARIPAVGSLSRDEEGRLTGHDRPRWIAKDGEGRTIGYAHAWRAPWSSPGVLYEQVIVDPNARHQGVGRALFDVVMAYTSEVRADRVIVDLRDDDPVSLAFATKRGFKQERHLFESCIELANLDRESLDYPAFANDSFQMMSLADRPGEAMEQQLYELYRATHEDIPGFEGEYMWYSEWRKWTLDKEDFERSLALLVLDGDRPIGVVQLTANPESESLYNSFTGVDAAYRGQGIARALKIQSIREAIKRGYRYIRTNNDSLNAPMLRINRSLGYQPVPGYYMMTRNIE
>NZ_CP045293.1|WP_152391870.1|298157_298586_+|GerAB/ArcD/ProY-family-transporter
MCKRFRTGSALVFPLNLDAKEAGWISKLLGMAAALIFYAVFCYIARDKPRQPFTVVIEGIIGKVPGKILASLYTLFFIYQASRQFNDFALLMSVSVFDQTPIIMIHAMMVVAIGYVLALGIVVLARTGEIFYVVMMSMIVLS

Crispr_ID: NZ_CP045293_3

• CRISPR_ID: NZ_CP045293_3
• CRISPR_location: 3209789-3210524
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 14 spacers

Consensus repeat of NZ_CP045293_3

Consensus_repeat	Method
TTAACTGCTTTTTNGCAGTTATT	CRT

spacers of NZ_CP045293_3

>3.1|3209812|28|NZ_CP045293|CRT
TGGGCGATTCGTGCGTTAGGCGGGCTAA
>3.2|3209863|28|NZ_CP045293|CRT
TGGACGATTAGAGCGAGCGGCGAGCCTA
>3.3|3209914|28|NZ_CP045293|CRT
CAGGCGGTTTGAGCGTTCGGCGAGCTAT
>3.4|3209965|28|NZ_CP045293|CRT
CAGGCGATCTGTGCGAGCGGCGAGCCTA
>3.5|3210016|28|NZ_CP045293|CRT
CGAGCGGTTTGAGCGAGCGGAGAGCCTA
>3.6|3210067|28|NZ_CP045293|CRT
CGCACGACTTGAGCGTTCGGCGAGCCTA
>3.7|3210118|28|NZ_CP045293|CRT
TGGGCGACTTGTGCGGGAAGCGAGCTAT
>3.8|3210169|27|NZ_CP045293|CRT
GAACGCTTTGAGCGAGCGGTGAGCCTA
>3.9|3210219|28|NZ_CP045293|CRT
CAGGCGACTTTAGCGTTCTGCGAGCTAA
>3.10|3210270|28|NZ_CP045293|CRT
TGGACGATTAGAGCAATCGGCGAGCCTA
>3.11|3210321|28|NZ_CP045293|CRT
CAGGCGACTTTAGCGTTTGGCGAGCAAT
>3.12|3210372|28|NZ_CP045293|CRT
CAGGCGGTTTGAGCGAGCGGTGAGCCTA
>3.13|3210423|28|NZ_CP045293|CRT
TGGGCGACTTGTGCGGGAAGCGAGCTAT
>3.14|3210474|28|NZ_CP045293|CRT
CGAACGCTTTGAGCGAGCGGTGAGCCAA

CRISPR arrays and Neighbor proteins around NZ_CP045293_3

CRISPR arrays

The CRISPR arrays of NZ_CP045293_3

>merge|NZ_CP045293|3|3209789-3210524|CRT
ATAACTGCTTTTTGGCAGTTGTTTGGGCGATTCGTGCGTTAGGCGGGCTAAATAACTGCTTTTTAGCAGTTATTTGGACGATTAGAGCGAGCGGCGAGCCTATTAACTGCTTTTTAGCAGTTATTCAGGCGGTTTGAGCGTTCGGCGAGCTATTTAACTGCTTTTTGGCAGTTATTCAGGCGATCTGTGCGAGCGGCGAGCCTATTAACTGCTTTTTTGCAGTTATTCGAGCGGTTTGAGCGAGCGGAGAGCCTATTAACTGCCTTTTGGCAGTTATTCGCACGACTTGAGCGTTCGGCGAGCCTATTAACTGCTTTTTTGCAGTTAATTGGGCGACTTGTGCGGGAAGCGAGCTATTTAACTGCTTTTTAGCAGTTATCGAACGCTTTGAGCGAGCGGTGAGCCTATTAACTGCTTTTTAGCAGTTATTCAGGCGACTTTAGCGTTCTGCGAGCTAAATAACTGCTTTTTAGCAGTTATTTGGACGATTAGAGCAATCGGCGAGCCTATTAACTGCCTTTTAGCAGTTATTCAGGCGACTTTAGCGTTTGGCGAGCAATTTAACTGCTTTTTAGCAGTTATTCAGGCGGTTTGAGCGAGCGGTGAGCCTATTAACTGCTTTTTTGCAGTTAATTGGGCGACTTGTGCGGGAAGCGAGCTATTTAACTGCTTTTTAGCAGTTATTCGAACGCTTTGAGCGAGCGGTGAGCCAATTAACTGCTTTTGGGCAGTTATT

>NZ_CP045293|3|1|3209789-3210524|CRT
ATAACTGCTTTTTGGCAGTTGTT	TGGGCGATTCGTGCGTTAGGCGGGCTAA
ATAACTGCTTTTTAGCAGTTATT	TGGACGATTAGAGCGAGCGGCGAGCCTA
TTAACTGCTTTTTAGCAGTTATT	CAGGCGGTTTGAGCGTTCGGCGAGCTAT
TTAACTGCTTTTTGGCAGTTATT	CAGGCGATCTGTGCGAGCGGCGAGCCTA
TTAACTGCTTTTTTGCAGTTATT	CGAGCGGTTTGAGCGAGCGGAGAGCCTA
TTAACTGCCTTTTGGCAGTTATT	CGCACGACTTGAGCGTTCGGCGAGCCTA
TTAACTGCTTTTTTGCAGTTAAT	TGGGCGACTTGTGCGGGAAGCGAGCTAT
TTAACTGCTTTTTAGCAGTTATC	GAACGCTTTGAGCGAGCGGTGAGCCTA
TTAACTGCTTTTTAGCAGTTATT	CAGGCGACTTTAGCGTTCTGCGAGCTAA
ATAACTGCTTTTTAGCAGTTATT	TGGACGATTAGAGCAATCGGCGAGCCTA
TTAACTGCCTTTTAGCAGTTATT	CAGGCGACTTTAGCGTTTGGCGAGCAAT
TTAACTGCTTTTTAGCAGTTATT	CAGGCGGTTTGAGCGAGCGGTGAGCCTA
TTAACTGCTTTTTTGCAGTTAAT	TGGGCGACTTGTGCGGGAAGCGAGCTAT
TTAACTGCTTTTTAGCAGTTATT	CGAACGCTTTGAGCGAGCGGTGAGCCAA
TTAACTGCTTTTGGGCAGTTATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045293.1|WP_152394172.1|3205998_3206712_+|cyclic-nucleotide-binding-domain-containing-protein	unknown	unknown	gnl|CDD|223736
NZ_CP045293.1|WP_152394178.1|3215334_3217941_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152394181.1|3221931_3224883_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|271155
NZ_CP045293.1|WP_152394182.1|3225244_3226648_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270451
NZ_CP045293.1|WP_152397250.1|3226947_3228081_-|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|380491
NZ_CP045293.1|WP_152394177.1|3214439_3215333_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|224096
NZ_CP045293.1|WP_152394167.1|3199704_3200415_-|purine-nucleoside-phosphorylase	unknown	unknown	gnl|CDD|180275
NZ_CP045293.1|WP_152394173.1|3207666_3208686_-|phosphotransferase	unknown	unknown	gnl|CDD|366736
NZ_CP045293.1|WP_152394170.1|3202971_3203730_-|TrmB-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197223
NZ_CP045293.1|WP_152394175.1|3210609_3213384_-|alpha-mannosidase	unknown	unknown	gnl|CDD|223460
NZ_CP045293.1|WP_152394165.1|3195424_3196981_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|223562
NZ_CP045293.1|WP_152394176.1|3213468_3214422_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223472
NZ_CP045293.1|WP_152394168.1|3200457_3201462_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|225263
NZ_CP045293.1|WP_152394179.1|3217978_3220042_-|DUF1282-domain-containing-protein	unknown	unknown	gnl|CDD|271320
NZ_CP045293.1|WP_152394180.1|3220057_3220930_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223472
NZ_CP045293.1|WP_152394171.1|3203862_3205725_-|bifunctional-metallophosphatase/5'-nucleotidase	unknown	unknown	gnl|CDD|236566
NZ_CP045293.1|WP_152394169.1|3201627_3202812_-|MFS-transporter	unknown	unknown	gnl|CDD|225371
NZ_CP045293.1|WP_152394174.1|3208712_3209471_-|DUF4184-family-protein	unknown	unknown	gnl|CDD|379379
NZ_CP045293.1|WP_152394166.1|3197149_3199387_-|bifunctional-2',3'-cyclic-nucleotide-2'-phosphodiesterase/3'-nucleotidase	unknown	unknown	gnl|CDD|236506
NZ_CP045293.1|WP_152397249.1|3220934_3221906_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|224096

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045293.1|WP_152394172.1|3205998_3206712_+|cyclic-nucleotide-binding-domain-containing-protein	gnl|CDD|223736	COG0664, Crp, cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases [Signal transduction mechanisms].	1.73381e-45
NZ_CP045293.1|WP_152397249.1|3220934_3221906_-|ABC-transporter-permease-subunit	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	2.73525e-51
NZ_CP045293.1|WP_152394181.1|3221931_3224883_-|extracellular-solute-binding-protein	gnl|CDD|271155	cd14489, CBM_SBP_bac_1_like, Putative Carbohydrate Binding Module (CBM) of extracellular solute-binding protein family 1. Domains in this family co-occur with extracellular solute-binding domains which are periplasmic components of ABC-type sugar transport systems involved in carbohydrate transport and metabolism. Carbohydrate binding modules of family 6 (CBM6), also known as cellulose binding domain family VI (CBD VI), and related CBMs (CBM35 and CBM36) are non-catalytic carbohydrate binding domains found in a range of enzymes that display activities against a diverse range of carbohydrate targets, including mannan, xylan, beta-glucans, cellulose, agarose, and arabinans. These domains facilitate the strong binding of co-occuring (catalytic) modules to their insoluble substrates.	3.59422e-66
NZ_CP045293.1|WP_152394182.1|3225244_3226648_-|extracellular-solute-binding-protein	gnl|CDD|270451	cd14748, PBP2_UgpB, The periplasmic-binding component of ABC transport system specific for sn-glycerol-3-phosphate; possesses type 2 periplasmic binding fold. This group includes the periplasmic component of an ABC transport system specific for sn-glycerol-3-phosphate (G3P) and closely related proteins from archaea and bacteria. Under phophate starvation conditions, Escherichia coli can utilize G3P as phosphate source when exclusively imported by an ATP-binding cassette (ABC) transporter composed of the periplasmic binding protein, UgpB, the transmembrane subunits, UgpA and UgpE, and a homodimer of the nucleotide binding subunit, UgpC. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised 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. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. 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.	5.28115e-39
NZ_CP045293.1|WP_152397250.1|3226947_3228081_-|GntR-family-transcriptional-regulator	gnl|CDD|380491	cd06267, PBP1_LacI_sugar_binding-like, ligand binding domain of the LacI transcriptional regulator family belonging to the type 1 periplasmic-binding fold protein superfamily. Ligand binding domain of the LacI transcriptional regulator family belonging to the type 1 periplasmic-binding fold protein superfamily. In most cases, ligands are monosaccharide including lactose, ribose, fructose, xylose, arabinose, galactose/glucose, and other sugars. The LacI family of proteins consists of transcriptional regulators related to the lac repressor. In this case, the domain sugar binding changes the DNA binding activity of the repressor domain.	2.35134e-63
NZ_CP045293.1|WP_152394177.1|3214439_3215333_-|ABC-transporter-permease-subunit	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.27016e-37
NZ_CP045293.1|WP_152394167.1|3199704_3200415_-|purine-nucleoside-phosphorylase	gnl|CDD|180275	PRK05819, deoD, DeoD-type purine-nucleoside phosphorylase.	7.83358e-142
NZ_CP045293.1|WP_152394173.1|3207666_3208686_-|phosphotransferase	gnl|CDD|366736	pfam01636, APH, Phosphotransferase enzyme family. This family consists of bacterial antibiotic resistance proteins, which confer resistance to various aminoglycosides they include: aminoglycoside 3'-phosphotransferase or kanamycin kinase / neomycin-kanamycin phosphotransferase and streptomycin 3''-kinase or streptomycin 3''-phosphotransferase. The aminoglycoside phosphotransferases inactivate aminoglycoside antibiotics via phosphorylation. This family also includes homoserine kinase. This family is related to fructosamine kinase pfam03881.	3.76846e-16
NZ_CP045293.1|WP_152394170.1|3202971_3203730_-|TrmB-family-transcriptional-regulator	gnl|CDD|197223	cd09124, PLDc_like_TrmB_middle, Middle phospholipase D-like domain of the transcriptional regulator TrmB and similar proteins. Middle phospholipase D (PLD)-like domain of the transcriptional regulator TrmB and similar proteins. TrmB acts as a bifunctional sugar-sensing transcriptional regulator which controls two operons encoding maltose/trehalose and maltodextrin ABC transporters of Pyrococcus fruiosus. It functions as a dimer. Full length TrmB includes an N-terminal DNA-binding domain, a C-terminal sugar-binding domain and middle region that has been named as a PLD-like domain. The middle domain displays homology to PLD enzymes, which contain one or two HKD motifs (H-x-K-x(4)-D, where x represents any amino acid residue) per chain. The HKD motif characterizes the PLD superfamily. Due to the lack of key residues related to PLD activity in the PLD-like domain, members of this subfamily are unlikely to carry PLD activity.	7.47708e-18
NZ_CP045293.1|WP_152394175.1|3210609_3213384_-|alpha-mannosidase	gnl|CDD|223460	COG0383, AMS1, Alpha-mannosidase [Carbohydrate transport and metabolism].	0
NZ_CP045293.1|WP_152394165.1|3195424_3196981_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|223562	COG0488, Uup, ATPase components of ABC transporters with duplicated ATPase domains [General function prediction only].	0
NZ_CP045293.1|WP_152394176.1|3213468_3214422_-|ABC-transporter-permease-subunit	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	8.2929e-59
NZ_CP045293.1|WP_152394168.1|3200457_3201462_-|helix-turn-helix-domain-containing-protein	gnl|CDD|225263	COG2390, DeoR, Transcriptional regulator, contains sigma factor-related N-terminal domain [Transcription].	1.31242e-112
NZ_CP045293.1|WP_152394179.1|3217978_3220042_-|DUF1282-domain-containing-protein	gnl|CDD|271320	cd05819, NHL, NHL repeat unit of beta-propeller proteins. The NHL(NCL-1, HT2A and LIN-41)-repeat is found in multiple tandem copies, typically as 6 instances. It is about 40 residues long and resembles the WD repeat and other beta-propeller structures. The repeats have a catalytic activity in Peptidyl-glycine alpha-amidating monooxygenase; proteolysis has shown that the Peptidyl-alpha-hydroxyglycine alpha-amidating lyase (PAL) activity is localized to the repeats. Tripartite motif-containing protein 32 interacts with the activation domain of Tat. This interaction is mediated by the NHL repeats.	3.79229e-27
NZ_CP045293.1|WP_152394180.1|3220057_3220930_-|ABC-transporter-permease-subunit	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.23572e-53
NZ_CP045293.1|WP_152394171.1|3203862_3205725_-|bifunctional-metallophosphatase/5'-nucleotidase	gnl|CDD|236566	PRK09558, ushA, bifunctional UDP-sugar hydrolase/5'-nucleotidase periplasmic precursor; Reviewed.	1.10825e-121
NZ_CP045293.1|WP_152394169.1|3201627_3202812_-|MFS-transporter	gnl|CDD|225371	COG2814, AraJ, Arabinose efflux permease [Carbohydrate transport and metabolism].	1.07797e-84
NZ_CP045293.1|WP_152394174.1|3208712_3209471_-|DUF4184-family-protein	gnl|CDD|379379	pfam13803, DUF4184, Domain of unknown function (DUF4184). This domain of unknown function contains several highly conserved histidines.	4.52709e-58
NZ_CP045293.1|WP_152394166.1|3197149_3199387_-|bifunctional-2',3'-cyclic-nucleotide-2'-phosphodiesterase/3'-nucleotidase	gnl|CDD|236506	PRK09420, cpdB, bifunctional 2',3'-cyclic-nucleotide 2'-phosphodiesterase/3'-nucleotidase.	0

Protein sequences

>NZ_CP045293.1|WP_152394174.1|3208712_3209471_-|DUF4184-family-protein
MPFTFAHPLYAYPLKSIKPKYFSLTGLILGSMAPDFEYFIMLEPYSWIGHSMAGLFFEALPLCTLLALIFHYIVKDVLAIHLPAIWQLDQRAYQIRGAWNLRGPRAWLIFLGSVALGFATHVLIDAFTHVSGYFVVRYAILREAVVWNIPVYKILQHSLSLLGLIVIGYVILTNLFRSNPNNSPVAPCATKKQKLQYWSIVIAIALAVTCIKLLLTSSQNQLGILVVAPVSGAVVGIIVASIRNKMIRSIGR
>NZ_CP045293.1|WP_152394173.1|3207666_3208686_-|phosphotransferase
MSNESNTSSLYAPISSEEIINIMKDTFGADCDVLHTSLLKGGLFNTTYLIETTSPEGKWVLRLAPQETEHLYSFEKQMMAVEPHIYRLLESEDIPSSRVIRYDESGSLIVRPYLIIEFIDSIPLNDPSILPEDYARLKEELGRYTRQMHHLTSDRFGWPQPDGTVRGYPTWSQMLLELSTEVVDRCSVYHVFEEQILQEFAAVFHDNAELFDEITVPSLVHNDLWDPNVLVRRGGDGELHIAALIDADRAVYADREYEFIVYENHPNFMQGYGYELSMEPRPRARRTAYQMMLSFLCAFVYEIQLAMPENATWCKKDALAQLQAFRELWSEATMEGRSE
>NZ_CP045293.1|WP_152394172.1|3205998_3206712_+|cyclic-nucleotide-binding-domain-containing-protein
MIEMNEVPIFSEVPAEELHSIAPLLRERKYKKNHVFMFENDQNEGIFILRTGKVKVYRIHEGREIVIGIHLPGDIIGEAEALTGDTYRVSSVEALEPVVAWHITKQDFLDIVHRYPSVLLRAYQIMFARVRVLNRMIRYLTFLDVRTKIANLILDLYYNFGKQVDNDYKIDMKFNHALLASMVGNTRESISKTLSDFQNEGLIDIRQKYIYLLDMKRLERMCYETEEVPELRIWHHG
>NZ_CP045293.1|WP_152394171.1|3203862_3205725_-|bifunctional-metallophosphatase/5'-nucleotidase
MKAKTILLTGALSTVFAASAFAAPLHPVVHNEWMQDKKIINGFDKGGLLLERSVSLGEAIALIARGTGAEIVQPQGYWATNYLTWAYSKGAITKDEKGNDRSFPSADRLMAIAKKLGLDLQLPAGEQVTRGDYVQALGDALTEHITIAHTNDVHGHIQENSKDKEFGYAKIATLVKEWREENKNFLLMDAGDTFQGTIYTNQFKGESILPILNSLGYGAMAAGNHEFDFGYEQLLKLRDQLKYPMINANVYKADGTNLLIPTYTAEIGGQKIAFIGFVTEETPIVTHPNNVIGLTFKDPVDIAKKLVPEMKEKADRVIILSHIGVEKDREIAKNVSGIDLIIGGHSHTPLRTPEVVNGTYIVQDWEYGKSLGRVDLYYYKKDLVGFSGGLVEYDESVKADPEVEKLVQDVVKKVDTAMAAVIGKTDVDLQGERNQVRAVETNLGNFIADAIIAKTKTIKGHEADVALVNGGGIRASKKAGDLTKKDLYSILPFPNTLTIVKATGADIKAALEVSVKGVEKKDDLPGSFLQIGGLSYVYDVTKPVGERVLEVKVGGQPIDPAKTYTVATNDFITSGGDGYSMLKKDQVLNTGYTFYDVVEEYLQNVKVINPKVENRIVEKK
>NZ_CP045293.1|WP_152394170.1|3202971_3203730_-|TrmB-family-transcriptional-regulator
MLHKFGFSQYESKVYEALVTSLQPMDATLIVKVSGVPKAKIYEVISRLVEKGMVLESISEKKKLYTALALPLVIEKLTAEFQSDLEELEARATPKVFIDDQVWSLKANSSIEPQLSQVLQEATKSIRFSGWRDDIAKYMPLLEAKEQEGVTVEVHAVGEVESNLTNLVYFVPSKEHVTLERFRLLIVDDREMIFAGVEQQEWQAIKTKSQPLVRVFTEFFNHDVLLSIITSKYIDVLMEDKDIMDRLMQLKY
>NZ_CP045293.1|WP_152394169.1|3201627_3202812_-|MFS-transporter
MNFKIYILAIACFVTGTVELIVGGILDLISQDLNISLSASGQLITIYSIAFALAGPILLAATAAVERKKLYMITLVTFIIGNLLSTFSPSFEVLLAARVLSAASSALIVVLSITMASQLVEPKYRARAIGTIYMGVSGSLVLGVPLGMMLGNAYGWRAPFMMISVLSLLALLAVGRFMTKAQPTPSVPLKQQLASLKNGKIVLAHLLSILMLTGHLTLYAYLTPFLQETLHLSASTLSLFYFIFGIAAVAGGGVGGWVSDRFGPEKSILFIVSAFAVMMFLMPLATFSIYVCLVVMMLWSMLSWSVSPALQSYLIKSAPESAEIQQSLNSSALHVGIALGSAVGGVVIEQASVYYNAWVGVIFVLFALVCAVLSIRWRQTRSTRVVAPVGESIS
>NZ_CP045293.1|WP_152394168.1|3200457_3201462_-|helix-turn-helix-domain-containing-protein
MDQEKIRKMIEAAKMYYFMDYSQQDIADKLGVSRPTVSRFLQQAKEDGLVQIRIMDPTEDTAKLAYELKQKYNLKKVIVVPVPHYEDDLIKEYLAEDTALYLDEIVKDGDTIGVTWGSTIYQVARKLKHKHVNQVNVVQLKGGVSQLETNTYNSEILHLFGKAYHTYPHFLPLPAIVDHLLVKQAMESDRHIRKILDLGEQANIALFTVGVAESDSLFLQMGYFSEEELQVIYKQAVGDICSRFYDVNGQICVPDLNARTIGIELEALKRKERSILVAGGARKVEAIFGALRGRYANVLVTDQFTAKSLLDKDHDVSSRMNTSTAFPLSGIPLY
>NZ_CP045293.1|WP_152394167.1|3199704_3200415_-|purine-nucleoside-phosphorylase
MSVHIGAMPSDIAESILLPGDPIRAKFIAETFLEESYCYNGVRGMLGYTGYYKGKRVSVQGTGMGVPSMSIYAHELIQEYGVKNMIRVGTCGAIQHDVKLRDIVIAMSASTSSAINQRRFNGIDFAPTANFHFLRKAYDLSQAKKLSVKVGNVMTTDTFYINNWDEIRLWADYQMLALEMETAELYTLATRHHVNALSILTVSNLVLTGEMTTAEERESTFTEMIELALDVAVTPD
>NZ_CP045293.1|WP_152394166.1|3197149_3199387_-|bifunctional-2',3'-cyclic-nucleotide-2'-phosphodiesterase/3'-nucleotidase
MNHKKMLKSLLAAALVSSAFSMSAFAEASDPGAKLKLRLMETTDIHTHIVNHDYYQDQSTEEFGLALTASLIMKARQEVTNSMLIDNGDLIQGNPLGDFVAKVRPLQEGQVHPVFKAQNLLEYDAAGIGNHEFNFGLEFLDRSLKGAKFPHVNANVYIDDHDNNPDNDKNYFKPYEILTRTFKDDKDAPVTLKIGVIGFVPPQIMEWDKANLEGKVIAKDIIETANKFVPKMKQEGADLIIAVPHSGFDSSPYKENMSDATVHLAKVPGIDAILFGHDHKVFPSKEFDNIEGIDIQKGTIHGVAAVMPGFWGDHLGVVDLTLEKKDGKWKVVDSQSEARPIYDKANKKSLAKVDERIVDAVKEEHAATVEFVRGPIGETTAPINSFFAVVHDDPSVQIVSNAQKWYTEKYIQGTSFEGIPVLSAAAPFKAGGRWGPNYFTDIPTGTLAVKSAADLYVYPNTVNVVQLNGDQVREWLEHAAGQFNQIDPSKKDEQPLINEDFPTYLYDVIDGVTYQIDVTKPARYDRKGKLVNPDSHRIVNLQFNGKPVTKDQQFLVATNNYRASGGGNFPNLDGSNIVISSPDETRQVLIDYIAQNKKINPTADNNWSFIPVTGDTNITFRTSPKAKDAATKLGGMKYVGEEKDGFAKFTLDLSKGAQPETTPMTDPSPVTSELVPVRETAGAHGITVAYDLKTKTVTLTHGAAIVSYVLNTDSALVNGTKVPVSAELKDNTLWLPASILQSLTS
>NZ_CP045293.1|WP_152394165.1|3195424_3196981_-|ATP-binding-cassette-domain-containing-protein
MSILNVERLSHGFGDRAIFNDVSFRLLKGEHIGLIGANGEGKSTFMNIITGKLQPDDGKVEWSKRMRVGYLDQHAVLSQGMTIRDVLRGAFQYLFDMEQEMNDMYGRMGEVSAEELEQLLEDVGTIQDTLTNQDFYMIDAKIEETARGLGITDIGLDKDVNDLSGGQRTKILLAKLLLEKPDILLLDEPTNYLDEQHIEWLKRYLQEYENAFILISHDIPFLNSVINLIYHMENQELTRYVGDYDHFQQVYEMKKSQLESAFKRQQQEIADLKDFVARNKASVATRNMAMSRQKKLDKMDVIELAKEKPKPQFNFKDSRASGKMIFETKDLVIGYDSPLSRPLDLRMERGQKIALVGANGIGKTTLLRSLLGEIPAISGTVQRGENLDIGYFQQEMKDTNYNTCIEEIWQEFPAFTQFEVRAALAKCGLTTKHIESKIAVLSGGEKAKVRLCKLINRETNLLVLDEPTNHLDVDAKDELKRALKAFKGSILLISHEPEFYRDVVTETWNCESWTTKVF
>NZ_CP045293.1|WP_152394175.1|3210609_3213384_-|alpha-mannosidase
MSQSKTVHIISHTHWDREWYLPYEKHHVLLIKLMDTLMETLERDEEYRSFHLDGQTIILEDYLQVRPEMRAKLEHYIREGRIHIGPWYILQDEFLTSSEANVRNLLIGHRDAAAYGTISKLGYFPDSFGNMGQAPQMLKQAGIQHAVFGRGVKPTGFNNEVTDVSAYESPYSEMWWESPDGSKVLGILFANWYSNGNEVPAEAEAAKIYWDKKLADAEKYASTRHLLFMNGCDHQPVQTDLSEAIKTAEQLYPDVTFVHSNFDDYLEQVGRSLPDNLSVIRGELRSQHTDGWGTLVNTASSRVYMKQKNQQGQTALEKVAEPLAAMAYMLGQSYPHHLFNYAWKTLMQNHPHDSICGCSVDEVHAEMMTRFEKSRHVAEAIADESLAWIADRADTSSFAAYGTDAVPFVVSNTTGWVRSGSLSVELEVKRIYFRSGMDFGQMRREVKEYNLDGFVLVDSDGVQLPCTVEDLGIQFGYDLPEDQFRQPYFARSVRVTFEAVAVPALGYRAYGVVRTTDAASNREAASLITDTNQMENDKLIVAVEVDGTLTVTDKSSGVVYRGLGTLEDTGDIGNEYMYREANGTAPITTRGVPAAAIHVVRDTPYQAAIEIVHELEIPIAADDLLELEQREIVWFTGRRAGRSSQMTTMRIVTHVSLNRHGEGVEVACSFNNQAKDHRLRMLFPTGLRVGTHYADSIFEVPERSSTPAEEWKNPSNCHHQQAFVTVSGEEAGLTIANQGLNEYEVIQGEAGDDTIAVTLLRAVGELGDWGYFPTPEAQCQGEHSVKLCIIPFTHEERSVDADPRDDAMGSIVQAYQFQVPWSTQQAEVHEGSLPATHSFVSWEGPSLAFSAMKVAEASGDIILRWFNVSTDVQALNVALHAEDDIVVYRSDILERQLERLVQAEDGALTAPIRPAEIVTLSFAK
>NZ_CP045293.1|WP_152394176.1|3213468_3214422_-|ABC-transporter-permease-subunit
MRVQAARMGEWLSRKSPQEKAKLWTWIAVRTLLILGFCYIILFPLFLRISVAFRSKVDIYDPTVLWIPRHFTFENLKLAISATKYGSALLNTFMISSATTIIQLATCALAGYAFARLKFKGSGILFALVIFTIVVPPQTIMIPLYLTYRYFDLFGILKWFTEKGSVNLIDTFWPFLISSGTAMGLKNGLYIYIFRQFFRGVPKELEEASLVDGAGIFKTFYRIILPNAIPAIVTVLLFSFVWQWNDSYYVSLFLSKVKVLATQLTDMGPALGKEPDPVYQSMLLNTGVLLMMAPLIVLYLFVQRYFVESVERTGLVG
>NZ_CP045293.1|WP_152394177.1|3214439_3215333_-|ABC-transporter-permease-subunit
MKRKSLTLEQKKAWYGVLFASPLIIGMIMLFLLPLIQSFRFSLSSIHIVESGFATEYKGFVNYISLFTSNPDYPRSLTESVAHMLVNVPIIIIFSLFAAVLLNQKFRGRSIARAIFFLPVILASSAIANLDISSFVGGTAMSGGGEGGANLLQSFELKKMLLESGMGPAIVDYITGAVDRIYEIISSSGVQILIFLAGLQSISPSLYEASKIEGATGYEIFWKVTFPMMTPLILTNLVYSIIDSFSSNKINTLISQTAFKTFDFGLSAAMSWVYFIVVAIILFVSTAIISRKVFYYD
>NZ_CP045293.1|WP_152394178.1|3215334_3217941_-|hypothetical-protein
MSGKLKISLGILSAGMVICGLIALGMPESESMDRTAQKAVQEIGSNTVKTKSYQNVKTASASGMVQSSSEKVTVNTAEELAALQQMKLVTQNETLMLYVNEETAVIAVKDKRDGYIWFSNPVDRDQDPIASPLYKSEMSAQLLVAYYNGKGQINTFNSFDDSVNKKQFKITNVDQGVKIIYQLGKISKSFANIPQKISKQRFDDMILSKLPDQDARDSMTYKFKLDEQTQIYEVRKLKDFVAEEISAKLTEIGYTNEEAAKDNAENGVTEAAEDDGPQFTIPLEYVLDGNELVARVPSQEIQYAKSYPIATLQVLKYFGAAHEKKQGYMFVPDGSGALIYLNNNKKNTEPYDMPVYGPDGTFDVKERIQTNEVTRMPVFGMKQNDHAMIGVIEAGDGLSSITADISGRNDSYNTIASKFNLVSMDFYTLTSGTKSSSVPMFQTKPYAGDYTVRYGFLSGSKANYSGMAGVYRDYLVKKYDMKKLEAKAEAPLVLEVEGAFQKQKSFLGVPYQSTESLTTFDEARELLSTLKEKGVQQVDMRYVGWFNGGIRHTSPTSVKAVGALGGNGDFRKLVDYAKQENIGLYPDVAFQAKYKGSSDAATFLDGQKASIYQYDPVMYVKDTLKFSHYLLSPAVLGETVDRFASKYATYDVPGVSLRDLGNELHSDFAKDQSVNRQEALQIAEEQVAKLKQQTKNVMVDGGNVYTLPSANVIVNAPIRSSQLNITDEDIPFYQMALHGYVDLAGAPMNAQHATDPRIPLLRAMETGSNLFYQWYAADASVIKDSDYNGLYGLHYQDWMDQAVANYQEVKSQLGAVRHQTITGHRKLAEGVVETTFEQGTRVIINYNNTPIQAEGHSIDGLGYWVGGE
>NZ_CP045293.1|WP_152394179.1|3217978_3220042_-|DUF1282-domain-containing-protein
MKRILALLFAITLFAGFTTPAAQAASDETYNYNYWGQTVPAPSPYEEQRVMYGRDWGMKELSSPQDIYVGSNRLIYIADTGNDRIIVLNDQFETARILSEFQHDGKTDTFNKPEGVFYNRYDGHLFIADTQNKRIVELDEEGKFVRQIGDPKSTLIREGFQYTPIKVIVDKAQRIYVISRGSYEGIMEFDTDGAFNGFIGTNRVKFSPVDLFWKRISTKSQREQMQLFIPLEFNNMDIDADGFIYTTTSEEKSDQPIKRLNASGVDILRDKGYFPPKGDIHTLDIGSAPGSSIFVDVVSDEGGIYNALDSKRGRIFTYDKDGNLLYVFGGLGSQQGKFRTPSAIAMLDDKLLVLDKDYNRLSLFRPTHYGSLIREAVISLYNGQAEQSTAAWQKVLQMNGNLEVAYIGIGKSLLKNGDNHGAMKYFELGNNRENYSEAFKRYRKEIVFDYFGMIVLTIALVIGGSIAAVKLAGRRKAQQHYVDVGSIKSPFYTMVHPFNGFWEMKYEKKGKVKIVLVMVALLVLFTIIKRQYSGFVVNFNNPNELNSINELKFIVLPFILWCVANWSLTTLMDGEGKFRDIVMATGYALMPFIIIYLPQTLYSNLITGSESSFYYILDAIAFIWFIWLLFIGTMTVHQYSASKTVVTMLLTLVVIGIMVFLGVLFFSMLQQMANFVISIYRELSFRF
>NZ_CP045293.1|WP_152394180.1|3220057_3220930_-|ABC-transporter-permease-subunit
MNMKLIMKKRLNRSWAVDLLLFLLLGSVAFFMAIPLIFTISNAFKPIDEIFVFPPRMLVRHPTLKNFTDLVNIFSDSWVPFSRYVFNTFFIAITGTVGHVIIASAAAYPLAKIRFPGRNFLFSIVVMSLMFTAYVTQVPNYMTISWLNLINTYWAILLPSFGMTLGLYLMKQFMEQIPDALLEAAKIDGASEYRIFWTIVMPIVKPAWLTLIIFSLQSLWTNGSVTSHKYIYSEQLKTVDYVFGQVASGGLVRTGPVAAVTLLMMAVPITVFIVTQSNIIQTMSTSGLKE
>NZ_CP045293.1|WP_152397249.1|3220934_3221906_-|ABC-transporter-permease-subunit
MNLNPIGPPETGRHGRVAALRALPARIGRVFREMKKNKHAYALIAPYFLIFGTFTVFPVLMSLALSFTSFNMLEPPKWVGWHNYARLFVQDDIFLIALKNTLLFALITGPISYMACFLFAWLINELPPKLRALLTLILYAPSISGNTYLIWQTLFASDSYGYANSFLMKWGVIMEPIQWLQDPRFMLGILILVQLWLSLGTSFLAFIAGLQNVDRTLYEAGAIDGVRNRWQELWFITLPAMRPQLLFGAVIQITLAFSVAEISIYMIGFPSVDYAAHTIVTHLVDYGSIRFEMGYASAIATVLFTMMLCTNLLTRKLLGKVGE
>NZ_CP045293.1|WP_152394181.1|3221931_3224883_-|extracellular-solute-binding-protein
MRRSSKKTVFILVTCIAIACTPLWWVGGEARQVASAEGSSSGMDQALLSTLTGTSKKGGYREYAALHNQANRPSEEIVIEADSFDRTQDMDVTVLDHFEGSTGRSVRTSDSGSIEWKFSVPQDGLYNIGLNYFTVKGKDSDIERELRIDGKIPFTEANSITFQRIWKDESTTFERDERDNDLLPSQIEVPMWQDMLLKDATGYVEEPYAFYFAKGEHTLTLTSVKEPLVIRSIKLTNPQTTPSYETIARTYKERGYKNAQQELKIQAEHATYKSSPTLLAYNDHSSPAVEPYHVSKLRNNAMGGWAWRLPGQWIEWEIDVPEDGLYQIALKNHQNYLRGMAALRTLYIDGQVPFEEVRHVPFPYNSEWQMTVLGKDAENPYEFYLTKGKHSIRFEVTLGDLAPILTAVESSILELNAIYREIISFTGTVPDTFRDYQLEQRIPDMVENFRKQSELLYRVAKTLTGPNGKNDDRTAMLNTLAYQLQDMADRPETVPSRVEQFKTNVGSLGAWLLSVNEQPLAIDYLMISTPKAELPDPTASTWLSLKSSTMAFFASFFENYDDFSEDKSDKAVTVWITSARDQAQTVKKLIDDTFTPKTGIPINIKLVSSDILLPSTVAGEGPDVALQVGNDLPVNYATRNAMQDLSVFPDFEQVKTRFNPSAMVPISYNGGVYALPETQTFPVLFYRKDILEDELHLKVPQTWDDVYEMLPVLQKHNLEFGLPQRGLNTFGNDTGTTDIITIGPNPALTMFLYQNDGELYRNNGMKSGLDSETAVQQFKKWTDFYVNYKIPIQADFANRFRTGEMPIGVIDYTMYNKLSVFAPEIKGLWAFAPVPGTKTADGTIRRETGSGGSATVMFKKTKNKEAAWEFMKWWTSKETQIAFGRQMEIRMGASARYPTANQEALSALPWPTKDFSILKEQMSWVQGVPEVPGGYLTGRNIENAFRRVVVQGDDAREALEYYVRYINEEITLKRQEFNLPTEK
>NZ_CP045293.1|WP_152394182.1|3225244_3226648_-|extracellular-solute-binding-protein
MKALKFASYFLTLMLIVSVIGCSKGTDTKPAAEPAAQQEDTTKTEPAKEEPAAAEEKKFDLNGQTVKIGVWWDDADPRTMKDKGPAEEAQIKLIEETEKKYNAKIEFVKFGDYGKYVENFTVTSLSGEPFADIVRLELFWAFPQLVNKEFIQPIDEWIDVKDAKYIDWMRAGGSYKGKQYGIIDSAPSPYGIFYNKTLVQKLGLEDPYELQQKGEWTWDKFREFAKKATKDTNGDGKTDVWGLSGAYGKLKALTEQMVYTNKGSVDKDESGEIKFSLNGPNAVEALQYVSDLFNVDKSIQQPIPDDASKEFVAGKGVMYAGFSWELGGFVENMKGQDLGYVFFPKGPKAEKYVSYTPFGNMWMVSKYSKNAEAALHIIDEISLNEAGRKLSEESWQTSYPNKESMDTRKQMADNIDYISYYAIPDGEKLFEGVVKEITEGKVSPATAIDKVKPQFEANIKKLLDSSK
>NZ_CP045293.1|WP_152397250.1|3226947_3228081_-|GntR-family-transcriptional-regulator
MILESEKQPLYMRILGDLQEKIRTGQYVPEQQLPTEVDLAEQYGVSRITSKRALIELEREGLIYRKRGSGSYVKHPEDANLSGETGSPVAHRIISMVLPYMATSELDYIKGAHDYLDSKGYFLTIHNSNWKKDKEREMITKIPKSGPSGIILYPISTISNIDVVHAIYSNDFPIVTIDQYFDSLPISSVVSDNFEGGYQTAKRLIELGHERIAFVSSVSVEYRSSVRDRYLGYCRALKDHRIPIDTELLITDFYTEMYSPNANAFYNTLLDRLLDLEVSAIQAEHDHLAVDLVRCCLDKGIQVPEQLAIAGFDDHDVSRQADVPVSSVAQNYYAIGYEAARMIVQRIEQPELAHQQVKVPIRIIERESTSQHVNTSV

Crispr_ID: NZ_CP045293_4

• CRISPR_ID: NZ_CP045293_4
• CRISPR_location: 3832684-3833431
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 14 spacers

Consensus repeat of NZ_CP045293_4

Consensus_repeat	Method
CANTTAACTGCTTTTTTGCAGTTATTTCGGCG	CRT

spacers of NZ_CP045293_4

>4.1|3832716|19|NZ_CP045293|CRT
GTGCGCGGCCTGGGCGCGG
>4.2|3832767|19|NZ_CP045293|CRT
GATCGAGGCCTGGACGCGG
>4.3|3832818|19|NZ_CP045293|CRT
GCACACGGCCTGGGCGCGA
>4.4|3832869|19|NZ_CP045293|CRT
GTGCGCGGCCTGGGCGCGG
>4.5|3832920|20|NZ_CP045293|CRT
AACCGCGGCCTGGGGCGCGG
>4.6|3832972|19|NZ_CP045293|CRT
GCACGCGGCCCGGGCGCGG
>4.7|3833023|19|NZ_CP045293|CRT
GCACGCGGCCCGGGCGCGG
>4.8|3833074|19|NZ_CP045293|CRT
GCACGCGGCCTGGGCGCGG
>4.9|3833125|19|NZ_CP045293|CRT
AACCGCTGCCCTGACGAGC
>4.10|3833176|19|NZ_CP045293|CRT
GTGCGCGGCCCGGGCGCGA
>4.11|3833227|19|NZ_CP045293|CRT
GTACGCGGCCCGGACGAGG
>4.12|3833278|19|NZ_CP045293|CRT
GTTCACGGGCGAGTCGCGA
>4.13|3833329|19|NZ_CP045293|CRT
AACCGCGACCTGGGCGCGA
>4.14|3833380|20|NZ_CP045293|CRT
ACGCGCGGCCTTGGGCACGC

CRISPR arrays and Neighbor proteins around NZ_CP045293_4

CRISPR arrays

The CRISPR arrays of NZ_CP045293_4

>merge|NZ_CP045293|4|3832684-3833431|CRT
GAAATAACTGCTTTTTTGCAGTTATTTCGGCGGTGCGCGGCCTGGGCGCGGCATTTAACTGCTTTTTTGCAGTTATTTCGGCGGATCGAGGCCTGGACGCGGCATTTAACTGCTTTTTTGCAGTTATTTCGACGGCACACGGCCTGGGCGCGACAATTAACTGCTTTTTTGCAGTTATTTCGGCGGTGCGCGGCCTGGGCGCGGCATTTAACTGCTTTTTTGCAGTTAATTCGGCGAACCGCGGCCTGGGGCGCGGCATTTAACTGCTTTTTTGCAGTTATTTCGGCGGCACGCGGCCCGGGCGCGGCATTTAACTGCCTTTTTGCAGTTATTTCGGCGGCACGCGGCCCGGGCGCGGCATTTAACTGCCTTTTTGCAGTTATTTCGGCGGCACGCGGCCTGGGCGCGGCATTTAACTGCTTTTTTGCAGTTATTTCGGCGAACCGCTGCCCTGACGAGCCAATTAACTGCTTTTTTGCAGTTATTTCGGCGGTGCGCGGCCCGGGCGCGACATTTAACTGCTTTTTTGCAGTTATTTCGGCCGTACGCGGCCCGGACGAGGCATTTAACTGCTTTTTTGCAGTTATTAGGACGGTTCACGGGCGAGTCGCGACAATTAACTGCTTTTTTGCAGTTATTTCGACGAACCGCGACCTGGGCGCGACAATGAACTGCTTTTATGCAGTTATTTCAGCAACGCGCGGCCTTGGGCACGCCCAATAACTGCTGTTCGGCAGTTATTTCGCAC

>NZ_CP045293|4|2|3832684-3833431|CRT
GAAATAACTGCTTTTTTGCAGTTATTTCGGCG	GTGCGCGGCCTGGGCGCGG
CATTTAACTGCTTTTTTGCAGTTATTTCGGCG	GATCGAGGCCTGGACGCGG
CATTTAACTGCTTTTTTGCAGTTATTTCGACG	GCACACGGCCTGGGCGCGA
CAATTAACTGCTTTTTTGCAGTTATTTCGGCG	GTGCGCGGCCTGGGCGCGG
CATTTAACTGCTTTTTTGCAGTTAATTCGGCG	AACCGCGGCCTGGGGCGCGG
CATTTAACTGCTTTTTTGCAGTTATTTCGGCG	GCACGCGGCCCGGGCGCGG
CATTTAACTGCCTTTTTGCAGTTATTTCGGCG	GCACGCGGCCCGGGCGCGG
CATTTAACTGCCTTTTTGCAGTTATTTCGGCG	GCACGCGGCCTGGGCGCGG
CATTTAACTGCTTTTTTGCAGTTATTTCGGCG	AACCGCTGCCCTGACGAGC
CAATTAACTGCTTTTTTGCAGTTATTTCGGCG	GTGCGCGGCCCGGGCGCGA
CATTTAACTGCTTTTTTGCAGTTATTTCGGCC	GTACGCGGCCCGGACGAGG
CATTTAACTGCTTTTTTGCAGTTATTAGGACG	GTTCACGGGCGAGTCGCGA
CAATTAACTGCTTTTTTGCAGTTATTTCGACG	AACCGCGACCTGGGCGCGA
CAATGAACTGCTTTTATGCAGTTATTTCAGCA	ACGCGCGGCCTTGGGCACGC
CCAATAACTGCTGTTCGGCAGTTATTTCGCAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045293.1|WP_152394643.1|3844290_3845403_-|citrate-synthase	unknown	unknown	gnl|CDD|184467
NZ_CP045293.1|WP_152394623.1|3821956_3823099_+|ROK-family-protein	unknown	unknown	gnl|CDD|366120
NZ_CP045293.1|WP_152394631.1|3830169_3831522_+|cytochrome-ubiquinol-oxidase-subunit-I	unknown	unknown	gnl|CDD|376587
NZ_CP045293.1|WP_152394640.1|3840902_3841175_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152394627.1|3825835_3826711_-|phosphate-ABC-transporter-permease-PstA	unknown	unknown	gnl|CDD|223654
NZ_CP045293.1|WP_152397299.1|3841230_3841890_+|sortase	unknown	unknown	gnl|CDD|320678
NZ_CP045293.1|WP_152394642.1|3842928_3844221_-|NADP-dependent-isocitrate-dehydrogenase	unknown	unknown	gnl|CDD|180792
NZ_CP045293.1|WP_152394624.1|3823119_3823746_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152394636.1|3834377_3836183_-|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|380161
NZ_CP045293.1|WP_152394629.1|3827671_3828622_-|phosphate-ABC-transporter-substrate-binding-protein-PstS-family-protein	unknown	unknown	gnl|CDD|270372
NZ_CP045293.1|WP_152394638.1|3838947_3839541_+|5'-deoxynucleotidase	unknown	unknown	gnl|CDD|378993
NZ_CP045293.1|WP_152394626.1|3825039_3825795_-|phosphate-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224042
NZ_CP045293.1|WP_152394628.1|3826715_3827645_-|phosphate-ABC-transporter-permease-subunit-PstC	unknown	unknown	gnl|CDD|223646
NZ_CP045293.1|WP_152394632.1|3831518_3832541_+|cytochrome-d-ubiquinol-oxidase-subunit-II	unknown	unknown	gnl|CDD|224213
NZ_CP045293.1|WP_152394635.1|3833530_3834256_-|response-regulator	unknown	unknown	gnl|CDD|223816
NZ_CP045293.1|WP_152394630.1|3828785_3829889_-|hypothetical-protein	unknown	unknown	gnl|CDD|206779
NZ_CP045293.1|WP_152394637.1|3837215_3838754_-|fumarate-hydratase	unknown	unknown	gnl|CDD|377546
NZ_CP045293.1|WP_152394625.1|3824352_3825006_-|phosphate-signaling-complex-protein-PhoU	unknown	unknown	gnl|CDD|273990
NZ_CP045293.1|WP_152394639.1|3839869_3840736_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|235853
NZ_CP045293.1|WP_152394641.1|3841959_3842901_-|malate-dehydrogenase	unknown	unknown	gnl|CDD|180477

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045293.1|WP_152394643.1|3844290_3845403_-|citrate-synthase	gnl|CDD|184467	PRK14034, PRK14034, citrate synthase; Provisional.	0
NZ_CP045293.1|WP_152394623.1|3821956_3823099_+|ROK-family-protein	gnl|CDD|366120	pfam00480, ROK, ROK family.	4.20435e-70
NZ_CP045293.1|WP_152394631.1|3830169_3831522_+|cytochrome-ubiquinol-oxidase-subunit-I	gnl|CDD|376587	pfam01654, Cyt_bd_oxida_I, Cytochrome bd terminal oxidase subunit I. This family are the alternative oxidases found in many bacteria which oxidize ubiquinol and reduce oxygen as part of the electron transport chain. This family is the subunit I of the oxidase E. coli has two copies of the oxidase, bo and bd', both of which are represented here In some nitrogen fixing bacteria, e.g. Klebsiella pneumoniae this oxidase is responsible for removing oxygen in microaerobic conditions, making the oxidase required for nitrogen fixation. This subunit binds a single b-haem, through ligands at His186 and Met393 (using SW:P11026 numbering). In addition His19 is a ligand for the haem b found in subunit II.	2.35662e-160
NZ_CP045293.1|WP_152394627.1|3825835_3826711_-|phosphate-ABC-transporter-permease-PstA	gnl|CDD|223654	COG0581, PstA, ABC-type phosphate transport system, permease component [Inorganic ion transport and metabolism].	3.26863e-89
NZ_CP045293.1|WP_152397299.1|3841230_3841890_+|sortase	gnl|CDD|320678	cd05829, Sortase_F, Sortase domain found in the class F family of sortases. Class F sortases are mainly present in Actinobacteria, Chlorobacteria and Firmicutes. Their functions are largely unknown.	5.02315e-59
NZ_CP045293.1|WP_152394642.1|3842928_3844221_-|NADP-dependent-isocitrate-dehydrogenase	gnl|CDD|180792	PRK07006, PRK07006, isocitrate dehydrogenase; Reviewed.	0
NZ_CP045293.1|WP_152394630.1|3828785_3829889_-|hypothetical-protein	gnl|CDD|206779	cd11386, MCP_signal, Methyl-accepting chemotaxis protein (MCP), signaling domain. Methyl-accepting chemotaxis proteins (MCPs or chemotaxis receptors) are an integral part of the transmembrane protein complex that controls bacterial chemotaxis, together with the histidine kinase CheA, the receptor-coupling protein CheW, receptor-modification enzymes, and localized phosphatases. MCPs contain a four helix trans membrane region, an N-terminal periplasmic ligand binding domain, and a C-terminal HAMP domain followed by a cytoplasmic signaling domain. This C-terminal signaling domain dimerizes into a four-helix bundle and interacts with CheA through the adaptor protein CheW.	9.48543e-38
NZ_CP045293.1|WP_152394636.1|3834377_3836183_-|HAMP-domain-containing-protein	gnl|CDD|380161	NF033092, HK_WalK, cell wall metabolism sensor histidine kinase WalK. This model describes WalK as found in Staphylococcus aureus (sp|Q2G2U4.1|WALK_STAA8). A shorter version, as found in Streptococcus pneumoniae, called WalK(Spn) or VicK, is not included. WalK is part of a two-component system and works with partner protein WalR.	9.21744e-100
NZ_CP045293.1|WP_152394629.1|3827671_3828622_-|phosphate-ABC-transporter-substrate-binding-protein-PstS-family-protein	gnl|CDD|270372	cd13654, PBP2_phosphate_like_2, Substrate binding domain of putative ABC-type phosphate transporter, a member of the type 2 periplasmic binding fold superfamily. This subfamily contains uncharacterized phosphate binding domains found in PstS proteins that serve as initial receptors in the ABC transport of phosphate in eubacteria and archaea. After binding the ligand, PstS interacts 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. The PstS proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	5.16037e-125
NZ_CP045293.1|WP_152394638.1|3838947_3839541_+|5'-deoxynucleotidase	gnl|CDD|378993	pfam12917, HD_2, HD containing hydrolase-like enzyme. This is a family of bacterial and archaeal hydrolases.	3.75857e-96
NZ_CP045293.1|WP_152394626.1|3825039_3825795_-|phosphate-ABC-transporter-ATP-binding-protein	gnl|CDD|224042	COG1117, PstB, ABC-type phosphate transport system, ATPase component [Inorganic ion transport and metabolism].	4.77318e-178
NZ_CP045293.1|WP_152394628.1|3826715_3827645_-|phosphate-ABC-transporter-permease-subunit-PstC	gnl|CDD|223646	COG0573, PstC, ABC-type phosphate transport system, permease component [Inorganic ion transport and metabolism].	2.00435e-92
NZ_CP045293.1|WP_152394632.1|3831518_3832541_+|cytochrome-d-ubiquinol-oxidase-subunit-II	gnl|CDD|224213	COG1294, AppB, Cytochrome bd-type quinol oxidase, subunit 2 [Energy production and conversion].	3.74098e-52
NZ_CP045293.1|WP_152394635.1|3833530_3834256_-|response-regulator	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	4.92761e-85
NZ_CP045293.1|WP_152394637.1|3837215_3838754_-|fumarate-hydratase	gnl|CDD|377546	pfam05681, Fumerase, Fumarate hydratase (Fumerase). This family consists of several bacterial fumarate hydratase proteins FumA and FumB. Fumarase, or fumarate hydratase (EC 4.2.1.2), is a component of the citric acid cycle. In facultative anaerobes such as Escherichia coli, fumarase also engages in the reductive pathway from oxaloacetate to succinate during anaerobic growth. Three fumarases, FumA, FumB, and FumC, have been reported in E. coli. fumA and fumB genes are homologous and encode products of identical sizes which form thermolabile dimers of Mr 120,000. FumA and FumB are class I enzymes and are members of the iron-dependent hydrolases, which include aconitase and malate hydratase. The active FumA contains a 4Fe-4S centre, and it can be inactivated upon oxidation to give a 3Fe-4S centre.	1.93196e-96
NZ_CP045293.1|WP_152394625.1|3824352_3825006_-|phosphate-signaling-complex-protein-PhoU	gnl|CDD|273990	TIGR02135, Uncharacterized_protein, phosphate transport system regulatory protein PhoU. This model describes PhoU, a regulatory protein of unknown mechanism for high-affinity phosphate ABC transporter systems. The protein consists of two copies of the domain described by pfam01895. Deletion of PhoU activates constitutive expression of the phosphate ABC transporter and allows phosphate transport, but causes a growth defect and so likely has some second function. [Regulatory functions, Other, Transport and binding proteins, Anions].	2.44985e-60
NZ_CP045293.1|WP_152394639.1|3839869_3840736_-|SDR-family-oxidoreductase	gnl|CDD|235853	PRK06701, PRK06701, short chain dehydrogenase; Provisional.	2.54543e-170
NZ_CP045293.1|WP_152394641.1|3841959_3842901_-|malate-dehydrogenase	gnl|CDD|180477	PRK06223, PRK06223, malate dehydrogenase; Reviewed.	0

Protein sequences

>NZ_CP045293.1|WP_152394632.1|3831518_3832541_+|cytochrome-d-ubiquinol-oxidase-subunit-II
MSYEILGITVLWIFLYGYLIVASIDFGAGFYSFFSLITGKRHRIHPIVERYLTPVWEVTNVFLVFFFVGIIGFFPETAYYYGTSLLVPGSIAIVLLAIRGVYYVYSQYGNRNNKFYMFLYGVSGLLIPASLSIVLTLSEGGYIHEQGGVVSLDYHALFTSAYSWSVVVLAIVSVLYISAMFLTYYAAKAKDKEALDILRSYALFWSVPTILCSLWVFFAIQRHNLDHFNKMVDNAWFFIASFICYVIAVYLVWKRSRLQLSFVMVMLQFGFAFFGYGKSHLPYILVPYLTLHEHFTNESMALALVIVFLLGLLVLVPSLYLLLRLFLFDASYVRGKLSKK
>NZ_CP045293.1|WP_152394631.1|3830169_3831522_+|cytochrome-ubiquinol-oxidase-subunit-I
MSHYDPVIYSRMLTTLTLAFHIIYATIGVGVPMLIALAEWMGIKRKDPHYLLLARRWARGYTITVAVGVVTGTAIGLQLSLLWPSFMLVAGQSIALPLFMETFAFFIEAIFLGIYLYTWNRFRNPMKHFMLLIPVVIGSSGSAFFITCVNAFMNTPRGFNISDTGKLTDVQPFLAMFTASMPTKAAHVLATAYVTASFILGAMAAMALLKGKNHVYYRKALKITMVAGLIFSLATILIGDLSGKYLAAYQPEKLAAGEWHFKTERYAPLIVGGILDDQNQVHYALKIPYALSILSHGLPSAEVQGLDETPKDLQPPLWIHYMFDLMVSIGMLLLFIGLWYVIAMRRRRKSGESARPLNKLLLSLIVVGAPLSVISIEAGWIYTEVGRQPWILVGFMKTVQGATKSEHVDLMLWIFAGLYLILGVSSAYVLRRMFKHHPAEEELKGGGSKA
>NZ_CP045293.1|WP_152394630.1|3828785_3829889_-|hypothetical-protein
MRGTAMSKVLMIHKFITVPSVLSPNQPCREVVQMIHRGIDSECLVVCNETTNEPMGLVMKDRFFRFLGKKYGADLYYEKPIAQIMDPNPLIVDIHIGPQEMIDKALNREEKHMYDCVIVTSQGQFVGVLTVGVLLHISRMQQQQSIQDQLGIAHSMEERIDQIHASVEEVASAADQGMKQSEEMVHLTLQGKSELDKVSKLFQHFAIQAERQEKQIDTLQQKTSSVTEISHFIREIAEKSNLLAVNAAIEAARAGEHGKGFAVVAAEVRKLADETKRSALAITEMIEQIAEAVTSTVRDVQSGREETANSALLVTEAKDLFEKLSHAAEENRLQASDIRHQSVIADKKTSEVTRSLSQIVEQLRKTS
>NZ_CP045293.1|WP_152394629.1|3827671_3828622_-|phosphate-ABC-transporter-substrate-binding-protein-PstS-family-protein
MMLVMLLIVAVALAACGGGKKEEAGAGTTDTGTEAAALSGTIEIDGSSTVFPLTEAAAEEFGKENSGVRVSVGTAGTGGGFKRFIKGEIAMSNASRPIKDKEAEEAKAAGIDYKELEVAYDGLSIVVNKENTWVDKLTLDELKKIYGPEATAKTWADVRAGWPADPIKIYSPGSEHGTFDYFTEVINGKAQESRNDKQITFAADTNSIVSGVEGDKASIGYFGFSFYEENQDKLKLVPIDNGTAVVSPSAETIKDNSYAPLSRPLYVYLNTKALEKPEVKAFTEYYLKNVANFAQEVGFIALPQEKYDEQIASLNK
>NZ_CP045293.1|WP_152394628.1|3826715_3827645_-|phosphate-ABC-transporter-permease-subunit-PstC
MNQAKERPGITSISFKNKKTYILDRAMPLFLFLCAAVSIVTTIGIVYTLLSETVDFFRKIPIFDFIFGTNWSPLIAPKAFGILPLLSGTMLITIIACLFAIPVGLACAIYLSEYAPTRVRKIVKPVLEVLAGVPTIVYGYFALTFVTPLIRTIFPDTGVFNALSAGLVVGIMIIPMVSSLSEDAMQAVPRSLRNGAYALGATRFEVALKVVVPAAFSGIVSSAVLAFSRAIGETMIVAVAAGATPKLTFNPLESIQTMTGYIVQVSLGDIPHGSIEYGTIYAVGMALFVITFLLNILALWVARRFREEY
>NZ_CP045293.1|WP_152394627.1|3825835_3826711_-|phosphate-ABC-transporter-permease-PstA
MSILQDANREQISRRRKTDWVLHILFVAATAIGVLALMALLVNIMMDGLSRLSPDLFTNYPSRMASKAGLKSAIVGSIYMVLIMTPLSFILGVGAAIYLEEYANKNWFTRLIQLNISTLAGVPSIVYGILGLTIFVRGMHLERSLLSGALTMTLLILPIIIVSSQEALRAVPRQRRDASFALGATRWQTVSGSVLPSAMPGIMTGVILALSRAIGETAPLVMIGALTFVAFLPNGIMDSFTVMPIQIFNWISRPQEAFHELAAAGIILLLGLLLIMNFSAILLRNKYSKNL
>NZ_CP045293.1|WP_152394626.1|3825039_3825795_-|phosphate-ABC-transporter-ATP-binding-protein
MNTLIDIKKLNLYYGTYHALKDVSLTIPEKAVTAFIGPSGCGKSTLLRTLNRMNDMIAGTKIEGAVEITGTDIYSNEVDVETLRKKVGMVFQQPNPFPKSIYDNIAYGPRLHGIRNKQKLDEIVEQSLRQSVLWDEVKDYLKRSAFSLSGGQQQRLCIARALAVNPDILLMDEATSALDPISTLKIEELVQELKDRYTIVMVTHNMHQAARVSDQTVFFLNGEVVEFAPTEQLFSNPSDQRTEDYITGRFG
>NZ_CP045293.1|WP_152394625.1|3824352_3825006_-|phosphate-signaling-complex-protein-PhoU
MPRKEFDSGLNELTKLLEAMGNETEQMLKESIESLQRLDVEHARALIARDSEINHMEERILDVGSKLILTQQPVAKDLRRILVAFKISSDLERMADLSVDIAKVVVRLEGQKLVKPLIDIPRMGEIVEQMIFESIRAYMEENVDLAYKMSKDDDAVDQLYSQIVRELFTLMVEDPKTVSQAMLLTFVGRYIERIADHATNIGESVVFLVTGKRPELN
>NZ_CP045293.1|WP_152394624.1|3823119_3823746_-|hypothetical-protein
MKKRHVFLFLLIISIIWLARDHLNQSFGELTFRAFGMSPWSEGTQGLHIPNSIGLMVLLIGFIGVVNSYRTIYPKIFSRLLIGVILLFAAIPWVTEHVMYLAHYNAKDTGTIQVVTKDRRAYIERNEAGDVTIRSQEFKIYNYGQATRMKVIPLTHDTEWREVTFDPFELQVEPHTQATFDTTFKGTDVKGAAYSHDSLIDIQVISVE
>NZ_CP045293.1|WP_152394623.1|3821956_3823099_+|ROK-family-protein
MKTTGDQFLVKKINKSIVLDTIREHSPISRAAVSKMTGLNKGTVSSLVQELIDNGLILEIGMGKSSGGRKPVMLLFHETAGYAIGVELGVTRVRTILTNLNGEMIEEDQLPLPTTDSERVIEVLFAAIQAMIERAPSSRYGVVGIGIGVPGIVDEKGQILFAPNLAWEHVDLHTLVSERFKLPVTIDNEANAGAVGELQYGAGRSAANIVYVSVSEGIGTGIMIGGELFRGAAGLSGEMGHMTIEANGRKCRCGNKGCWELYASSSAHPDYDFKTLLRMATEGEADGIRGFYDIGEYLGIGISTIINTFNPELIIIGNQISRAERYITSAIQQTVAARSLSYHRKQTTIRFAQLETRSTLLGAAYYAISGFFSKDRATLV
>NZ_CP045293.1|WP_152394635.1|3833530_3834256_-|response-regulator
MPQKILIIEDEPTLARLLSYNLSQDGYEITVIDHGTEGLQAALQKMYDLIILDIMLPGMNGFEILSRIRQSGMRTPIIILTARNAEEEVVQGLKHGADDYITKPFGVAELLARVSAVLRRTTGDESALTQAATKENVIHAGELLIYPEKYEVVLHGEAIPLRPKEFEVLLYLVQRPGMVITRDDLMNVVWGFDYIGGQRTVDVHVSSLRKKLEMNQQSVQIDSIRGVGYKLVMNKKVSTTR
>NZ_CP045293.1|WP_152394636.1|3834377_3836183_-|HAMP-domain-containing-protein
MKKFKVRLTVIMIVLIGLSMAASGFYMVQVFKRSHIEALEENMTREIKIIDTTFHWDQIQSTEPEAIKQLTEESHLISKSSGARVTFIRQDGKVLGDSDHDPASMDNHLDRQEVMNAQTKGFGSEIRYSNTLGENMLYVALPVHNKPYFEGYVRLAMSIQDVEASIRALWIYLSVGLAIMFVLAGMISYRIAHNLTRPIEKITRVAHQIKHMNYRSRVDVKNVDEIEQLGSAINAMADSLQTQMNLIRENENRLKNVLEHMINGIVMVDPTGKIVLVNQMAEMILGKETGYLLGHRYTEVKQQYELTKMIAEGLEKREVMRDEVTIYFPEERLLEIDVVPMIWEDEFGGILVLMQDLSAIRRLERMRSEFVANVSHELKTPIAAVKGFAETLLSGAVNDPATANSFLQIIYDESERLNRLIGDILELSKIESKRVPLQFSPVELHSFVESTVDVLRTEASKKLIDLQVQVPEHLYAEADEDRLRQIILNLVSNGISYTPEGGAVKVTLEPVDVNAAGDYERIRFIISDTGIGIPKADLPRIFERFYRVDKARSRSSGGTGLGLSIVKHLVDSHDGTISVESEIGVGTRFIIEIPVVQEHAF
>NZ_CP045293.1|WP_152394637.1|3837215_3838754_-|fumarate-hydratase
MQQFEESVYQLIVETSTNLPADVRRAVKKAREAEDQATRAGIALSTIAQNIEMAECNVSPICQDTGMPTFIVHTPVGTNQIVMKQQIKHAIQRATKNGKLRPNSVNSLTGANSGDNIGPGVPVIHFEQWERDEIDVRLILKGGGCENKNIQYSLPTELEGLGKAGRDLDGIRKCIMHAVYQAQGQGCSAGFIGVGIGGDRTTGYELAKQQLFRHVDDVNEIEDLAKLEDYILENANKLGIGTMGFGGQVSLLGCKIGVMDRLPASFFVSVAYNCWAYRRQGVLINAESGEIQEWIYEQGTEVTMNDAAEEEVREVKGAERREVVLTTPITEEQIRSLRVGDVVVINGEMHTGRDALHKYLMDHDAPIDLNGAVIYHCGPVMMKDEEGWHVKAAGPTTSIREEPYQGDIIKKFGIRAVIGKGGMGAKTLAALQEHGAVYLNAIGGAAQYYAQCLNKVNGVDFMEFGIPEAMWHLQVEGFAAIVTMDSHGNSLHADVEQDSLTKLSQFKDPVFK
>NZ_CP045293.1|WP_152394638.1|3838947_3839541_+|5'-deoxynucleotidase
MEKHFSAYMYRLRYIERWSLMRNVMPENVAEHSYHVALLTHMLCTIGNQEFNRQVDTHQAVTMALFHDATEVFTGDIPTPVKHHNPRILANFREIEDIASERLISMVPAKLLPVYEPLLDSKADQHSELRKYVKAADLLDAYLKCVTELTAGNREFAEAKRQTEEKLQQLSMPEVDYFLTYLAPSFEKTLDELSETE
>NZ_CP045293.1|WP_152394639.1|3839869_3840736_-|SDR-family-oxidoreductase
MPQSKQKAINPPQHQNQQPGIEAEMTPRPAFEGKHYKPAGKLAGKKAIISGGDSGIGRAVALAFAKEGADVAILYLNEEQDAQETKQSVEQLGRQCIAIGGDIGEEHFCKTAVKQVIDAWGQLDIVVNNAAEQYPQKSLSDITTAQLLRTFKTNIFGYFHLTKMALPHLKQGSSIVNTASITAYKGSPELIDYSATKGAIVSFTRSLAGSLVAQGIRVNGVAPGPIWTPLIPASFDEQKVSTFGSDTPMGRPGQPEELAASYVFLASEDASYITGQMIHVNGGDIVNG
>NZ_CP045293.1|WP_152394640.1|3840902_3841175_+|hypothetical-protein
MKKIAAAVLSACLVLSVASVASAAPAEQHPKHKMHAKSHHKMHAKSHKMHAKSTHKTKKLHAKSHKKGHIKMKGLTPKALPKTGFGGVSE
>NZ_CP045293.1|WP_152397299.1|3841230_3841890_+|sortase
MTPKQRNSFIIAIVMTLLFVGCSTRPSAEVKPQVLPKNQPTQEMAPLQPKTESLPPSAASSIAVKSEKAVRTGIIPNKILIPSVRIQTSVEPVGVLDNGQMEVPESTERVGILMNGVKAGEQGNAVIAGHVDNYTGPAIFYGLKKLKKDDPIILSDASGKYLVYKVLSVESFKTAEAPIDRVFGKTDESRLNLITCTGKYDRKKKEHEKRLIVFARLMK
>NZ_CP045293.1|WP_152394641.1|3841959_3842901_-|malate-dehydrogenase
MAIQRKKITVVGAGFTGATTALMLAQKELGDVVLLDIPQLENPTKGKALDMLEASPVQGFDSNIIGTSNYEDTADSDIVIITAGIARKPGMSRDDLVSTNASIVRSVCENIKKYCPDSIVIILSNPVDAMTYAAFETLGFPKNRVIGQSGVLDTARYCTFIAQELHVSVEDVRGFVLGGHGDDMVPLVRYSNVGGIPIEKLIPADRIEAIVQRTRVGGGEIVNLLGNGSAYYAPAASLVQMAEAIIKDKKRIIPVIALLEGEYGYHNLFLGVPTILGGNGIEKVFELELTADEKAALDKSADSVRNVIKVVQG
>NZ_CP045293.1|WP_152394642.1|3842928_3844221_-|NADP-dependent-isocitrate-dehydrogenase
MQLEKFALPTEGDKITIDNGKLQVPSNPIIPFIEGDGTGRDIWKASKRVLDAAVEKAYNGDKKIAWYEVFAGEKAFNAYGEWLPNDTLTAIREYIVAIKGPLTTPIGGGIRSLNVALRQELDLYTCLRPVRYFDGVPSPVKRPELVDMVIFRENTEDIYAGIEYASGSAEVKKVLEFLQQEMGVKKIRFPETSGIGIKPVSEEGSKRLVRAAVEYAIKHGRKSVTLVHKGNIMKFTEGAFKNWGYEVAEQEFGDKVFTWDQYDRIKAADGVDTANKAQADALAAGAILVKDAIADIALQQVLTRPTDFDVIATLNLNGDYLSDALAAQVGGIGIAPGANINYVTGHAIFEATHGTAPKYADLDVVNPGSVILSGVMLLEHLGWQEAADLIYKGMETSINNKTVTYDFARLMEGATEVKCSAFADEIIKNM
>NZ_CP045293.1|WP_152394643.1|3844290_3845403_-|citrate-synthase
MTATKGLEGIVATTSSISSIIDGALTYRGYNIDDLAVNASFEEVIYLLWFGRFPVQAELDQLLRDLSESAAIPAELVDQMRLYPSGTNTMAALRSAVSALALYDETANDMSPEANTRKAIKLQAQLPTIVAALSRLRAGLEPIAPKAGVSIAHNFLYMLNGEEPSELAVKALNQALVLHADHELNASTFAARVTVATLSDIYSGVTSAIGALKGPLHGGANEAVMVMLEEIGSFDRVEDYVQTKLDNKEKIMGFGHRVYKNGDPRAKHLQKMSQNLSELQGNTELYDMSVRIEEMVTGQKGLKPNVDFYSASVYTILGIQRELFTPIFAISRVSGWTAHILEQYENNRLIRPRAEYTGLTNQKYVPIQNR

Crispr_ID: NZ_CP045293_5

• CRISPR_ID: NZ_CP045293_5
• CRISPR_location: 4522977-4523260
• CRISPR_type: TypeI-A
• Repeat_type: NA
• Spacer_info: 5 spacers
• Cas_protein_info: csa3

Consensus repeat of NZ_CP045293_5

Consensus_repeat	Method
TAACTGCTTTTTTGCAGTTAATTTAG	CRISPRCasFinder
TAACTGCTTTTTTGCAGTTAATNTAG	CRT

spacers of NZ_CP045293_5

>5.1|4523003|25|NZ_CP045293|CRISPRCasFinder,CRT
CGGAAACATGACTTGCCGAGCAAAA
>5.2|4523054|26|NZ_CP045293|CRISPRCasFinder,CRT
ACGCTAGTGTGACCGATCGAGTGAAT
>5.3|4523106|26|NZ_CP045293|CRISPRCasFinder,CRT
GCCGACTCGCGCCCAACCGAGCTAAT
>5.4|4523158|25|NZ_CP045293|CRISPRCasFinder,CRT
TCGGAACGCGGCCTATCGAGCGGAA
>5.5|4523209|26|NZ_CP045293|CRISPRCasFinder,CRT
ATGCTAGCGTGGCCGATCGAGTGAAT

CRISPR arrays and Neighbor proteins around NZ_CP045293_5

CRISPR arrays

The CRISPR arrays of NZ_CP045293_5

>merge|NZ_CP045293|5|4522977-4523260|CRISPRCasFinder,CRT
TAACTGTTTTTTTGCAGTTAATTTAGCGGAAACATGACTTGCCGAGCAAAATAACTGCTTTTTTGCAGTTAATTTAGACGCTAGTGTGACCGATCGAGTGAATTAACTGCTTTTTTGCAGTTAATCGAAGCCGACTCGCGCCCAACCGAGCTAATTAACTGCTTTTTTGCAGTTAATTTAGTCGGAACGCGGCCTATCGAGCGGAATAACTGCTTTTTTGCAGTTAATTTAGATGCTAGCGTGGCCGATCGAGTGAATTAACTGCATTTTTGCAGTTATTGTAG

>NZ_CP045293|5|3|4522977-4523260|CRISPRCasFinder
TAACTGTTTTTTTGCAGTTAATTTAG	CGGAAACATGACTTGCCGAGCAAAA
TAACTGCTTTTTTGCAGTTAATTTAG	ACGCTAGTGTGACCGATCGAGTGAAT
TAACTGCTTTTTTGCAGTTAATCGAA	GCCGACTCGCGCCCAACCGAGCTAAT
TAACTGCTTTTTTGCAGTTAATTTAG	TCGGAACGCGGCCTATCGAGCGGAA
TAACTGCTTTTTTGCAGTTAATTTAG	ATGCTAGCGTGGCCGATCGAGTGAAT
TAACTGCATTTTTGCAGTTATTGTAG

>NZ_CP045293|5|3|4522977-4523260|CRT
TAACTGTTTTTTTGCAGTTAATTTAG	CGGAAACATGACTTGCCGAGCAAAA
TAACTGCTTTTTTGCAGTTAATTTAG	ACGCTAGTGTGACCGATCGAGTGAAT
TAACTGCTTTTTTGCAGTTAATCGAA	GCCGACTCGCGCCCAACCGAGCTAAT
TAACTGCTTTTTTGCAGTTAATTTAG	TCGGAACGCGGCCTATCGAGCGGAA
TAACTGCTTTTTTGCAGTTAATTTAG	ATGCTAGCGTGGCCGATCGAGTGAAT
TAACTGCATTTTTGCAGTTATTGTAG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045293.1|WP_152395180.1|4511685_4512651_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|226967
NZ_CP045293.1|WP_152395190.1|4526111_4529225_-|glycoside-hydrolase	unknown	unknown	gnl|CDD|367090
NZ_CP045293.1|WP_152395196.1|4533074_4533644_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152395186.1|4518984_4520895_+|arginine--tRNA-ligase	unknown	unknown	gnl|CDD|223097
NZ_CP045293.1|WP_152395187.1|4520990_4521737_-|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|225130
NZ_CP045293.1|WP_152395179.1|4510945_4511506_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152395185.1|4517618_4518542_-|ArsR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|238042
NZ_CP045293.1|WP_152395184.1|4515586_4517320_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|173853
NZ_CP045293.1|WP_152395189.1|4523372_4526108_-|alpha-mannosidase	unknown	unknown	gnl|CDD|223460
NZ_CP045293.1|WP_152395198.1|4536362_4536761_+|DUF2871-family-protein	unknown	unknown	gnl|CDD|378551
NZ_CP045293.1|WP_152395197.1|4533999_4536228_+|MMPL-family-transporter	unknown	unknown	gnl|CDD|225272
NZ_CP045293.1|WP_152395193.1|4530514_4530895_+|metalloregulator-ArsR/SmtB-family-transcription-factor	csa3	COG0640_csa3_CAS-I-A	gnl|CDD|223713
NZ_CP045293.1|WP_152395181.1|4512643_4513627_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|223521
NZ_CP045293.1|WP_152395195.1|4531614_4532994_+|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|274368
NZ_CP045293.1|WP_152395191.1|4529564_4529780_-|hypothetical-protein	unknown	unknown	gnl|CDD|227095
NZ_CP045293.1|WP_152395188.1|4521891_4522320_+|AsnC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224439
NZ_CP045293.1|WP_152395182.1|4513636_4514563_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|224094
NZ_CP045293.1|WP_152395183.1|4514574_4515528_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223674
NZ_CP045293.1|WP_152395192.1|4530086_4530518_+|SRPBCC-domain-containing-protein	unknown	unknown	gnl|CDD|176856
NZ_CP045293.1|WP_152395194.1|4530937_4531618_+|response-regulator	unknown	unknown	gnl|CDD|223816

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP045293.1|WP_152395193.1|4530514_4530895_+|metalloregulator-ArsR/SmtB-family-transcription-factor	csa3	COG0640_csa3_CAS-I-A	5.7e-19	63.4	0.3

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045293.1|WP_152395180.1|4511685_4512651_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|226967	COG4608, AppF, ABC-type oligopeptide transport system, ATPase component [Amino acid transport and metabolism].	8.88647e-147
NZ_CP045293.1|WP_152395190.1|4526111_4529225_-|glycoside-hydrolase	gnl|CDD|367090	pfam02449, Glyco_hydro_42, Beta-galactosidase. This group of beta-galactosidase enzymes belong to the glycosyl hydrolase 42 family. The enzyme catalyzes the hydrolysis of terminal, non-reducing terminal beta-D-galactosidase residues.	2.01969e-08
NZ_CP045293.1|WP_152395186.1|4518984_4520895_+|arginine--tRNA-ligase	gnl|CDD|223097	COG0018, ArgS, Arginyl-tRNA synthetase [Translation, ribosomal structure and biogenesis].	1.99657e-123
NZ_CP045293.1|WP_152395187.1|4520990_4521737_-|MBL-fold-metallo-hydrolase	gnl|CDD|225130	COG2220, COG2220, Predicted Zn-dependent hydrolases of the beta-lactamase fold [General function prediction only].	2.52416e-17
NZ_CP045293.1|WP_152395183.1|4514574_4515528_-|ABC-transporter-permease-subunit	gnl|CDD|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	3.91836e-117
NZ_CP045293.1|WP_152395185.1|4517618_4518542_-|ArsR-family-transcriptional-regulator	gnl|CDD|238042	cd00090, HTH_ARSR, Arsenical Resistance Operon Repressor and similar prokaryotic, metal regulated homodimeric repressors. ARSR subfamily of helix-turn-helix bacterial transcription regulatory proteins (winged helix topology). Includes several proteins that appear to dissociate from DNA in the presence of metal ions.	2.28476e-09
NZ_CP045293.1|WP_152395184.1|4515586_4517320_-|ABC-transporter-substrate-binding-protein	gnl|CDD|173853	cd00995, PBP2_NikA_DppA_OppA_like, The substrate-binding domain of an ABC-type nickel/oligopeptide-like import system contains the type 2 periplasmic binding fold. This family represents the periplasmic substrate-binding domain of nickel/dipeptide/oligopeptide transport systems, which function in the import of nickel and peptides, and other closely related proteins. The oligopeptide-binding protein OppA is a periplasmic component of an ATP-binding cassette (ABC) transport system OppABCDEF consisting of five subunits: two homologous integral membrane proteins OppB and OppF that form the translocation pore; two homologous nucleotide-binding domains OppD and OppF that drive the transport process through binding and hydrolysis of ATP; and the substrate-binding protein or receptor OppA that determines the substrate specificity of the transport system. The dipeptide (DppA) and oligopeptide (OppA) binding proteins differ in several ways. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Similar to the ABC-type dipeptide and oligopeptide import systems, nickel transporter is comprised of five subunits NikABCDE: the two pore-forming integral inner membrane proteins NikB and NikC; the two inner membrane-associated proteins with ATPase activity NikD and NikE; and the periplasmic nickel binding NikA, which is the initial nickel receptor that controls the chemotactic response away from nickel. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand binding domains of ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	1.28351e-118
NZ_CP045293.1|WP_152395189.1|4523372_4526108_-|alpha-mannosidase	gnl|CDD|223460	COG0383, AMS1, Alpha-mannosidase [Carbohydrate transport and metabolism].	0
NZ_CP045293.1|WP_152395198.1|4536362_4536761_+|DUF2871-family-protein	gnl|CDD|378551	pfam11070, DUF2871, Protein of unknown function (DUF2871). This family of proteins has no known function.	1.65472e-44
NZ_CP045293.1|WP_152395197.1|4533999_4536228_+|MMPL-family-transporter	gnl|CDD|225272	COG2409, COG2409, Predicted drug exporters of the RND superfamily [General function prediction only].	2.54607e-84
NZ_CP045293.1|WP_152395193.1|4530514_4530895_+|metalloregulator-ArsR/SmtB-family-transcription-factor	gnl|CDD|223713	COG0640, ArsR, Predicted transcriptional regulators [Transcription].	2.69516e-16
NZ_CP045293.1|WP_152395181.1|4512643_4513627_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.6837e-179
NZ_CP045293.1|WP_152395195.1|4531614_4532994_+|HAMP-domain-containing-protein	gnl|CDD|274368	TIGR02966, Phosphate_regulon_sensor_protein_PhoR, phosphate regulon sensor kinase PhoR. Members of this protein family are the regulatory histidine kinase PhoR associated with the phosphate ABC transporter in most Proteobacteria. Related proteins from Gram-positive organisms are not included in this model. The phoR gene usually is adjacent to the response regulator phoB gene (TIGR02154). [Signal transduction, Two-component systems].	2.94616e-63
NZ_CP045293.1|WP_152395191.1|4529564_4529780_-|hypothetical-protein	gnl|CDD|227095	COG4753, COG4753, Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain [Signal transduction mechanisms].	4.24807e-07
NZ_CP045293.1|WP_152395188.1|4521891_4522320_+|AsnC-family-transcriptional-regulator	gnl|CDD|224439	COG1522, Lrp, Transcriptional regulators [Transcription].	1.9764e-29
NZ_CP045293.1|WP_152395182.1|4513636_4514563_-|ABC-transporter-permease-subunit	gnl|CDD|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	2.59384e-95
NZ_CP045293.1|WP_152395192.1|4530086_4530518_+|SRPBCC-domain-containing-protein	gnl|CDD|176856	cd07814, SRPBCC_CalC_Aha1-like, Putative hydrophobic ligand-binding SRPBCC domain of Micromonospora echinospora CalC, human Aha1, and related proteins. This family includes the SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain of Micromonospora echinospora CalC, human Aha1, and related proteins. Proteins in this group belong to the SRPBCC domain superfamily of proteins, which bind hydrophobic ligands. SRPBCC domains have a deep hydrophobic ligand-binding pocket. MeCalC confers resistance to the enediyne, calicheamicin gamma 1 (CLM), by a self sacrificing mechanism which results in inactivation of both CalC and the highly reactive diradical enediyne species. MeCalC can also inactivate two other enediynes, shishijimicin and namenamicin. A crucial Gly of the MeCalC CLM resistance mechanism is not conserved in this subgroup. This family also includes the C-terminal, Bet v1-like domain of Aha1, one of several co-chaperones, which regulate the dimeric chaperone Hsp90. Aha1 promotes dimerization of the N-terminal domains of Hsp90, and stimulates its low intrinsic ATPase activity, and may regulate the dwell time of Hsp90 with client proteins. Aha1 can act as either a positive or negative regulator of chaperone-dependent activation, depending on the client protein, but the mechanisms by which these opposing functions are achieved are unclear. Aha1 is upregulated in a number of tumor lines co-incident with the activation of several signaling kinases.	1.85595e-27
NZ_CP045293.1|WP_152395194.1|4530937_4531618_+|response-regulator	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	1.56199e-77

Protein sequences

>NZ_CP045293.1|WP_152395188.1|4521891_4522320_+|AsnC-family-transcriptional-regulator
MNDVTIDAVDLDILQLLIEDANRSHKEIGQSVHLTGQAVGARVRKLQDIGVIEGYTVRWNPEKLGQAVQALVTVFLTSHTAHQRFRAFVDSSDEIVEAHRVSGEGCYWMRIRVGSPSALSAFLEQLLEFANYKVSLTIDQVK
>NZ_CP045293.1|WP_152395187.1|4520990_4521737_-|MBL-fold-metallo-hydrolase
MKIQLIRNATLWLEYAGVKILVDPMFSDAEANPPIINSNNDRRNPLVPLPADAAVWAQPDLMLVSHLHQDHFDEAAIARLPKTTPVVCQPGNEEQLHGHGFTDVTSIESTISTNGITIHRTQGQHGTGEIGQWMGQVSGFVLQAANEPTLYIAGDTIWCDDVVQALDAYHPDVTVVNAGGAQFVMGDPITMDAADVIAVCEHAPYTQVVAVHMDAINHCHVTRDKLRDALDASGKSYNVRIPEDGEWV
>NZ_CP045293.1|WP_152395186.1|4518984_4520895_+|arginine--tRNA-ligase
MRLQTFIITHIEQAITRLYQLSLNSEEGGKPQAAVRIEQPSHMEHGDYSTNIAMQLAKVLRKSPMILASEIAAQLEQEGKLEQLVEKIEVAPPGFINLFIDWSVWASRDWQLEQRRAQKAIVEHTSINPNKSAHIGHLRNACIGDSIVRLLNRAGVQVEVHNYIDDLGNQLADTVVGMLHTPLKNEHARFGDFCWDVYSSLHREYKVRPDLEQERSTVLHALEEGHNNTAWMGMLVAERIVREQLEEMEQFGIGYHLLVWESNIVREGFWDAAFQLLQQTPQFKQETAGKLAGCWVLKQGDTNHEAQGDADQLEGDHEHQLDKVLVRSNGILTYTAKDIAYHLWKFGLLGKDFGYKRFADGLYTTTAASLGAPVADAFGHADTVINVIDARQAYPQMMVKQALEVLGFQDQADQLRHISYGVVSLSPRSAADLGIDTSDGKSAYAMSGRQGIGIKISRLLDLMEQVIADNRSNPDGLSSRLIAAASIRYYLLRFNLQTEVVFDLQQATEISGNTGVYLLYAYARASTLMHRASAEHGITPQLPAAFPDLHRAEYALLRQLALWPDTLHAAVEELSPSLICTYAHELATLFNNFYGACPILKGDDASKAFRVWLTSRFHETLGDALNTLGLPTPERM
>NZ_CP045293.1|WP_152395185.1|4517618_4518542_-|ArsR-family-transcriptional-regulator
MALDYRLRVSFTPLHEFISSLHTYLCRKSYKKIDLSMDWVETTQERLSPELRDMLGNTEVNGDWRFIYLLALVCPDSTSPEELVAWIEGHSVGELYELLSQYGNEFPAQMEAFRTHAVQLLTAWNEEYFRQLDPEIIQLLHAEATRRTEMLTQLSPEDFVDDTTNGMLFTPIPGLEELILVPQYHFQPLNVIWHFGKVTLCHYAARVYVDEPGELSPHHYRILRTIGEKSRMKILRYLHNGPQPFTEIVRHLKISKGITHDHIGKLRSAGFIHAHIEGEVTTHYSLRLKAIRQIDEILYRYIATISQ
>NZ_CP045293.1|WP_152395184.1|4515586_4517320_-|ABC-transporter-substrate-binding-protein
MRKGLFSVLTVIISGALLLSACSSPASTPAADSGKTEAGATTSEQTPTPAAGGITSLVKATDLAKLPENAKKRTDTIIVGLTDPSGAFTPFFHQSGYDGNVSSVLYSSLVKVDEKGLPIPGLAEKWDISDDQLTYTYHLRKDLKFSDGSPLTADDVAFTWTILHDKAYDGQYDILSTNIKGGKAYKEGKASSIEGIKIIDPLTISVTLEKVNATALTVLGTDVLSKAYYGKDYKFGQLDYIKNLHAKPLGNGPYKLDKFIPGQEVRFVANENYYAGKPKTEHFIYKTTEGDAFQFIETGEQDYGSFQATTDNIDRLQKLGFLNLEPYTASNYGYLQFNMEHEALKDKLVRQALTYGLDRQTIYVDSNQGAATIANIPTQQSSWAYTEEGINPYKYDPEKAKQLLDEAGWKEGTDGIREKDGKKLSIHFIGSKKKGTDIFIAVAKENYAAIGVQLEAEQFADFNAQIAKFESGDYDLVSFSTSILGDPSEGVMSFVDGEVKGYDNPKVKELYTKGLATTDIEERKAIYKELYQVINEDAPYIFTSYSKLILAYNGRIENIKINPSQGISASLPEWTLK
>NZ_CP045293.1|WP_152395183.1|4514574_4515528_-|ABC-transporter-permease-subunit
MSTYLTKRLIYMVLILLGASMLIFFLYALTPGDFVSSNMKLTAERKAELREIYGLNKPLIDRYLLWMKNALHGDFGYSLAQQKPVLTLFNEYIWNSFLLAITSTFFTWLLAVIIGVISAYRQYSWFDTLVMIGIFAAMSIPSFFIGLFLIKTLAVDLKWLPPGGMMTTGSNATGLAYIKEVINHMALPVIVMTLLGVGSLTRYFRSNMIDVIKQDYIRTARAKGMTEKKVLFRHALRNALLPAITLVGFELPGLFGGSLIIEKIFNWPGIGQLYMQSFGARDYPLLMGFTMFIAVLTVIGTLISDILYNIADPRVKL
>NZ_CP045293.1|WP_152395182.1|4513636_4514563_-|ABC-transporter-permease-subunit
MAMVQGEVVKGRSSKLPAVRTSLWTQSMRKLLKNKLAVSGFIFIVFMFVACFIGPFFSPYTDGKVNVTAMNNAPNLKHWLGTDMLGRDVLTRLLQAGRISLTVGLASMLLSVFIGSLLGAIAGYYRGIVDQIIMRIADLLLSIPSLPILFILGALLSEWKIPTDYRMYIVMMMLSFVGWPGLARLVRGQMLSLREREFMQAAVVLGLRDRRKLFHHLLPNLFPLLIVVATLNIGGAILSESVLSYFGLGVMPPTATWGNMIDAANSIIDFEKHPWLWIPPGFAIFSTVIAINIFGDGLRDVLDPKHKK
>NZ_CP045293.1|WP_152395181.1|4512643_4513627_-|ATP-binding-cassette-domain-containing-protein
MKNTLEIDHLSTYFYTEEGTVKAIDDISLRVREGETVCIVGESGCGKSMTAMSIMGLIEGPAGKVVNGRIGFEGEDLLKMSKNEMRTIRGHDIAMIFQEPMSSLNPVLPIGQQITEPLIEHLKMSKKEARKRAIELIEQVGISRAEQIFHSYPHELSGGMLQRIMIAIAISCNPKLLIADEPTTALDVTIQAQILDMLRDIKSHSNMSILLITHDLGVVAEMADYVIVMYSGKIVEEGEVVELFNNPRHPYTQGLLKSKPIINQRQDQLYSIPGQVPNPLTLTESCYFHDRCGQCMAICESKEPQLRDIADRQKVACWLYEEAAVHV
>NZ_CP045293.1|WP_152395180.1|4511685_4512651_-|ATP-binding-cassette-domain-containing-protein
MSEPIVEVRNLKKYFPITGGLFNRTIGHVKAVDDISLSIRAGETFGLVGESGSGKSTVGRTILRLTDKTSGEVLFKGIDLHTLAPKELRKLRPQMQLIFQDPYSSLNPRVRVGDAIGEALLDHGLLQKGEIRDRVEEVLAACGLSSYHYDRFPHEFSGGQRQRIGIARALVLNPDLIIADEPVSALDVSIQAQIINLFRGLQESQGLTYLFISHDLSVVEHLCTRIGVMYLGSMMETAPRDELFRNPLHPYTKALLSAVPIPIPKLKRDRIVLKGDIPSPANPPSGCKFHTRCPFATEQCKAEAPAFRHVGHDHYVACHLV
>NZ_CP045293.1|WP_152395179.1|4510945_4511506_-|hypothetical-protein
MDFQVERQAFHSSTDEGLVWVCFKPIITTYKAMMRENETIGRDGVVAKVQFYRELTPGQQALFMYCSYHHHAIESQAEFYWWSAYFIAQPMFWTSLKKAVQYFEEDTMLLLLEEIEKIFTSQHDTHHELDDKLMFAAISPLDQMFHQFAPATLQRIGARIRQNPSAFVQIVDEAAASSTPESLRMF
>NZ_CP045293.1|WP_152395189.1|4523372_4526108_-|alpha-mannosidase
MEQRRTAHIISHTHWDREWYLPYEKHHVRLVELVDALLDKLDQDPEFKSFCFDGQTIILEDYLQVRPGQRERLTKYIQEGRIIIGPWYILQDAFLTSGEANVRNMQVGHEDSKRFGEPAKIGYFPDTFGLVGQTPQLMQQSGITNAFFGRGVKPTGFNNTVSDGGYESSFSELTWEGPDGSKVLGILFANWYSNGNEVPTDKEEAKKFWDRKLADAEKYASTRELLFMNGCDHQPIQLDVPEAIRVAKELYPDTEFVHSNFIDYLAAVEGAMEKELSSVRGELRSQRTDGWGTLVNTASARVYLKQMNQTGQMLLEKVAEPLATFADLLGRPYPHDLLTYAWKTLMQNHPHDSICGCSVDEVHREMVTRFDKSRHVAESIVDASARTIADAIDTTGFSAHGEEPLPLVVFNTTGWSRTGVVSVELEVAKIYERDVLSAKERTERMKAVSLAGRVLVDTEGNAIPCTVEDLGVVFDYDLPNDKFRQPFLTRKVRLTFEAEGIPAMGLKTYAWVKRDEEASQLSSLVTGERSMANHLLQVEITGDGSFALTDKRTGRVFTDLGVYESTGDIGNEYMYKQPDGEQALTTRGLPAQIRVLEDSAYRASFEIVHAWEIPASAEELLEIEQRELVGWSVRKAQRSTKMVPFTIRTVLTLDRHGRGLQIETSYNNQAKDHRLRALFPTNVTASVHDVDSMFEIAKRSIEPAPEWTNPSNAQHQQAFVDVSEAGAGLTVANFGLNEYEVLRDGRNTIAVTLLRSVGELGDWGYFPTPEAQCIGEHTVRMEVIPHDGDGIASGAYAEAYQFQVPWTACQTGVQAGRVSAVCAPFSWESPAAAFSSLKMNPETGDMMLRWYNMSEQPVDMALQASIGTAQLYKTTILEQPAEPFASDATDGVTLPLGPCEIVTIGVKPARA
>NZ_CP045293.1|WP_152395190.1|4526111_4529225_-|glycoside-hydrolase
MSTKAIFFFDPSFPNIHAEGISVEALAKFGTVVGAEGLAAALQGAEGGCFVNMHAPYFPKAAWNGIIQYLKNGGGLLSVGGAPFKHPVREENGKWIVEAEQTGYHQELYIHEALQVSADKVVRVEASAAYPLLADYAGLFPVEDSWNLVPHTTKNADLPLQMGSAGTMSTQITPLLIGKSAEDRELSAPVVLWENSRGTFVGSRWVFVHAPLHASFWAQGGADVLAKLAAFCGKGLTEISIKPNYANYEAGERPLLTLQTQNLQRNAEAVEGWTFDLTLTHQDEEAPCWTHCVEAEARCEQQYVRIPVPIEIRSGLYQLCATATSASGEVRVLRQGFWGHDAALLREGEPVSANRDYFVKDGRPLPVVGMTYMTSDVARKFLFLPNVDVWDRDMAQMKKAGINWIRTGVWTAYRNIMQVDGHASEEVLRAIDAFILTAKRHDLQLTFTFFSFTPETWEGVNPYLDPQSVEAQKRFIRAIVSRHRDTVNVDWDLINEPSMFAPEKIFSAGPRSAHDPYEREAYRTWLQERHGSIELLQERWNMSPVQLPSFDVILPPEEEEINFDVQNMHQGKKGTRWLDYCLFSMDMHNRWAKELTDTIKDIVPNHLVTVGQDEALGAQRPSPFFYEEAVDYTTVHSWWLNDQLVWDGIFAKTANKPNMIQETGIMYVETPDGRAKRSEFELRSILERKYAYAFSTGGAGAIQWIWNTNFYMDNANESHIGALRADGTEKPEADVSYDFGQFMNENRDLFEDRKLEDIAVIFPYSNDFSNRKFAFDATTRITRVMNYSLKWPFRGTSEYHLEDLRVNPAKLIVLPSAHNIDDKAMEQLVEIVKETGATLLITGPVGIGAYWQTSNRLNDVFGERKLGNVRREEMLLIGDKRYRVSFGQRRIAQLAKEVPAVQQASDGDAIVEVMVGQGRIIWSPLAVELNERDEVIEALYRYAAGQAGVSPVMDWLTGSELPGVYGQKLAFKNGNVYIFVSEYAWDAPVEIKDPVSGMTYRFTLPAERSILFATDQAGQLVSTYRPQEVNIEVKGRE
>NZ_CP045293.1|WP_152395191.1|4529564_4529780_-|hypothetical-protein
MGTSIQEHGSNVIQRFRVWFERANFLVLITDKKIYEIATEIGFRKLDTFYKRFKTYTGKSAGEIRAESGMT
>NZ_CP045293.1|WP_152395192.1|4530086_4530518_+|SRPBCC-domain-containing-protein
MTTNTPETLPDIVKEIEFNAPIQKVWDSVSSAEGIAAWFMPNDFEPVLGHKFTITSTYAVSPCEVLEIDPPNKLVFSWGEDWVITFELRAIEDRTAFTLIHGGWVDKVAPDTGIPYSVARDRMNGGWDSAVLPRLKAYVEGTA
>NZ_CP045293.1|WP_152395193.1|4530514_4530895_+|metalloregulator-ArsR/SmtB-family-transcription-factor
MTAAPKYDIFQAIADPTRRKLLHLLAEEKELPVSVISSNFPMSRTAVSKHLHVLESAGLVSERKIGRETRYRLHAAPLRELKDWLAYYEQFWDNKLAMLKHLVEAADEELKSERNPSNVTGPLKPL
>NZ_CP045293.1|WP_152395194.1|4530937_4531618_+|response-regulator
MRIHILVADDDPHIRELLRFILEKEGYVPHEAEDGEQAMHILEHEQVHLAVIDVMMPGKTGLELCEEIRRHHDLPVILLTAKGEMEDKEKGFLSGTDDYMVKPFEPKELLFRIRALLRRYQLVSAETIKLGRTLIDRRSYEIHAGGDTLVLPLKEFELLSHLASNPGRIFTREQLLQAIWGSDYEGDSRTIDVHIKRLRERFHDRPEDFIITTVRGLGYKLEVTET
>NZ_CP045293.1|WP_152395195.1|4531614_4532994_+|HAMP-domain-containing-protein
MRTLYVRIVMIFLLITFLGGILALIVTNFYYLGHIRDSNEKKIMSIGEDIRSLYVQNPDMELGSYLTHIANLGYQIYAVDSDLNGTYYGTPFKHKQFNGEHIKHVLQGGVYNGIKQESQWLKINSLFENSLRNSVGLPVQVHGEPYALFIRPNMEQQIGEVRIILALLIGFSFLFSIILIVVLSRFIVKPIKKLTDATHRIVGGDYRMELDVTRRDEIGNLARDFTHMARSIKQLDNMRQEFVANVSHEIQSPLTSIQGFAQSILEKKTTPEEEERYLRIIEEESRRLSSLSKQLLTLATLDKEDHILKRSSFRLDEQIRQIFIVTEQQWSDRDLELDLDLAEVVVSADQQLLYQVWYNLITNAIKFTNPGGMLRVTLAAEARLAVVRIADSGIGIPEDELAHIFDRFYKADKTRTRAQGGSGLGLSIARKVTTLHGGRIEVASRLGEGTEFTVRLPVG
>NZ_CP045293.1|WP_152395196.1|4533074_4533644_+|hypothetical-protein
MIGITALGQLFRCIATNPRQLTDFLQLFQRIAADSSHLTAFLQLFRRIAANTSQLTAFGQLFRRIAANTSQLTDFWQLFRRIAVKPSQLTAFWQLFRRISTNPRQLTDFLQLFRCIATNPRQLTAFLQLFRRVAASSSQLTVFWQLFRRIATNTSQLTDFGQLFRRIAANTSQLTAYGQLFRRITASAS
>NZ_CP045293.1|WP_152395197.1|4533999_4536228_+|MMPL-family-transporter
MHRFFQSLANRISTRKGAWTVLTIWLVVIIVLSGVAPSSKKYAVSSGEGSIHENTPSAIAEQLMNEQFPTEDGPVGLLVFHAKQAITTEQRAKISEVSTWLASDQKPVHVSSALPFHKFPKQVQDQMFSEDQTTLLLNIALDKNLDSAQLYDTMQLIRDKVAQIDMLDMQFEITGPAGIAADTTSLFKNADFVLMFATVGLILIILIVIYRSPLMAVIPLIIAGLVYQVTDRILGLAAKNEWFVVDKQALSIMMILLFAVLTDYCLFIVARYREALKTMDSKYEAMRVAFGQVAEPIAFSGGTVLIAMLTLFAAIFKPYHNFAPVFSVAMVVILLGGLTLIPAIYTLFGRRGFWPFMPKQELHTAPKKKPGFWARMGGVVTRKPGITSGILLLFLILSSINVTGMNYSFNLMKSFPSDTSSRQGFELLEEQFPPGQLAPVTVLLQSNKEIVIDAAYIEKLTKLTKALEAEGGIHDIRPNVTPALAAPDAKLPDKFISDQKHTLQLKVTLQANPYDPEALDVVRNLQDKSESILEQADFDPAQNTLHFAGQTAQQLDVRGMNAQDTIVTFSLVTLLIALMLTFQARSIKFAVTMIVTMLLSYTATLGLGWIVFHDILGYDAISYRLPVYTFVFLIALGVDYNIMLVSRIREEAKHHPWTEAISRGVAKTGGVISSAGIILAATFCVLITQPLQELFLFGFTMAMGILIDTFLVRGMLLPALMTLLGPRSTSVKTPLHQDHTRS
>NZ_CP045293.1|WP_152395198.1|4536362_4536761_+|DUF2871-family-protein
MKKSYYAAFFYLIIGMLSGVFYREYTKYSNFDGQSVLSVAHTHLLVLGFLFFLVVLILCKLFEIHKHKQFNLWFIVYNVAFIIMIGALIARGILQIEGSDFAGLPHIAGLSHTIMFVALIWLLLLFRKKIKE

Crispr_ID: NZ_CP045293_6

• CRISPR_ID: NZ_CP045293_6
• CRISPR_location: 4933525-4933633
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045293_6

Consensus_repeat	Method
TCATTTTTAGAATCAATTTCTTCAT	CRISPRCasFinder

spacers of NZ_CP045293_6

>6.1|4933550|59|NZ_CP045293|CRISPRCasFinder
TTAGTCTTCTTATATGTGAGTTCCTTTCATCTACTTCTTGCTGCAAACGAACAATTAAA

CRISPR arrays and Neighbor proteins around NZ_CP045293_6

CRISPR arrays

The CRISPR arrays of NZ_CP045293_6

>merge|NZ_CP045293|6|4933525-4933633|CRISPRCasFinder
TCATTTTTAGAATCAATTTCTTCATTTAGTCTTCTTATATGTGAGTTCCTTTCATCTACTTCTTGCTGCAAACGAACAATTAAATCATTTTTAGAATCGATTTCTTCAT

>NZ_CP045293|6|4|4933525-4933633|CRISPRCasFinder
TCATTTTTAGAATCAATTTCTTCAT	TTAGTCTTCTTATATGTGAGTTCCTTTCATCTACTTCTTGCTGCAAACGAACAATTAAA
TCATTTTTAGAATCGATTTCTTCAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045293.1|WP_152395466.1|4922540_4924151_-|lipopolysaccharide-biosynthesis-protein-RfbH	unknown	unknown	gnl|CDD|237960
NZ_CP045293.1|WP_152395465.1|4921715_4922510_-|glucose-1-phosphate-cytidylyltransferase	unknown	unknown	gnl|CDD|133015
NZ_CP045293.1|WP_152395480.1|4948060_4948702_+|transcriptional-regulator	unknown	unknown	gnl|CDD|377981
NZ_CP045293.1|WP_152395477.1|4940453_4941323_-|UTP--glucose-1-phosphate-uridylyltransferase-GalU	unknown	unknown	gnl|CDD|224131
NZ_CP045293.1|WP_152395478.1|4941449_4944074_-|U32-family-peptidase	unknown	unknown	gnl|CDD|223896
NZ_CP045293.1|WP_152395482.1|4949925_4951530_+|amidohydrolase-family-protein	unknown	unknown	gnl|CDD|226179
NZ_CP045293.1|WP_152395464.1|4920654_4921719_-|CDP-glucose-4,6-dehydratase	unknown	unknown	gnl|CDD|274236
NZ_CP045293.1|WP_152395479.1|4944557_4946453_-|hypothetical-protein	unknown	unknown	gnl|CDD|377924
NZ_CP045293.1|WP_152395470.1|4927515_4928103_-|SIS-domain-containing-protein	unknown	unknown	gnl|CDD|184408
NZ_CP045293.1|WP_152395481.1|4948793_4949891_+|amino-acid-aldolase	unknown	unknown	gnl|CDD|143494
NZ_CP045293.1|WP_152395473.1|4930190_4931045_-|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|212494
NZ_CP045293.1|WP_152397379.1|4934423_4935689_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213187
NZ_CP045293.1|WP_152395467.1|4924292_4925657_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152395469.1|4926818_4927514_-|NTP-transferase-domain-containing-protein	unknown	unknown	gnl|CDD|133065
NZ_CP045293.1|WP_152397380.1|4946473_4947622_-|trypsin-like-serine-protease	unknown	unknown	gnl|CDD|273938
NZ_CP045293.1|WP_152395476.1|4936647_4939116_+|O-antigen-ligase-domain-containing-protein	unknown	unknown	gnl|CDD|377422
NZ_CP045293.1|WP_152395472.1|4929144_4930161_-|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|187570
NZ_CP045293.1|WP_152395468.1|4926337_4926826_-|D-glycero-beta-D-manno-heptose-1,7-bisphosphate-7-phosphatase	unknown	unknown	gnl|CDD|319806
NZ_CP045293.1|WP_152395475.1|4935704_4936499_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|224596
NZ_CP045293.1|WP_152395471.1|4928103_4929132_-|dehydrogenase	unknown	unknown	gnl|CDD|225325

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045293.1|WP_152395466.1|4922540_4924151_-|lipopolysaccharide-biosynthesis-protein-RfbH	gnl|CDD|237960	PRK15407, PRK15407, lipopolysaccharide biosynthesis protein RfbH; Provisional.	0
NZ_CP045293.1|WP_152395465.1|4921715_4922510_-|glucose-1-phosphate-cytidylyltransferase	gnl|CDD|133015	cd02524, G1P_cytidylyltransferase, G1P_cytidylyltransferase catalyzes the production of CDP-D-Glucose. Alpha-D-Glucose-1-phosphate Cytidylyltransferase catalyzes the production of CDP-D-Glucose from alpha-D-Glucose-1-phosphate and MgCTP as substrate. CDP-D-Glucose is the precursor for synthesizing four of the five naturally occurring 3,6-dideoxy sugars-abequose (3,6-dideoxy-D-Xylo-hexose), ascarylose (3,6-dideoxy-L-arabino-hexose), paratose (3,6-dideoxy-D-ribohexose), and tyvelose (3,6-dideoxy-D-arabino-hexose. Deoxysugars are ubiquitous in nature where they function in a variety of biological processes, including cell adhesion, immune response, determination of ABO blood groups, fertilization, antibiotic function, and microbial pathogenicity.	1.40956e-167
NZ_CP045293.1|WP_152395480.1|4948060_4948702_+|transcriptional-regulator	gnl|CDD|377981	pfam08348, PAS_6, YheO-like PAS domain. This family contains various hypothetical bacterial proteins that are similar to the E. coli protein YheO. Their function is unknown, but are likely to be involved in signalling based on the presence of this PAS domain.	9.10892e-56
NZ_CP045293.1|WP_152395477.1|4940453_4941323_-|UTP--glucose-1-phosphate-uridylyltransferase-GalU	gnl|CDD|224131	COG1210, GalU, UDP-glucose pyrophosphorylase [Cell envelope biogenesis, outer membrane].	0
NZ_CP045293.1|WP_152395478.1|4941449_4944074_-|U32-family-peptidase	gnl|CDD|223896	COG0826, COG0826, Collagenase and related proteases [Posttranslational modification, protein turnover, chaperones].	3.11211e-114
NZ_CP045293.1|WP_152395482.1|4949925_4951530_+|amidohydrolase-family-protein	gnl|CDD|226179	COG3653, COG3653, N-acyl-D-aspartate/D-glutamate deacylase [Secondary metabolites biosynthesis, transport, and catabolism].	1.58012e-121
NZ_CP045293.1|WP_152395464.1|4920654_4921719_-|CDP-glucose-4,6-dehydratase	gnl|CDD|274236	TIGR02622, CDP-glucose_46-dehydratase, CDP-glucose 4,6-dehydratase. Members of this protein family are CDP-glucose 4,6-dehydratase from a variety of Gram-negative and Gram-positive bacteria. Members typically are encoded next to a gene that encodes a glucose-1-phosphate cytidylyltransferase, which produces the substrate, CDP-D-glucose, used by this enzyme to produce CDP-4-keto-6-deoxyglucose. [Cell envelope, Biosynthesis and degradation of surface polysaccharides and lipopolysaccharides].	0
NZ_CP045293.1|WP_152395479.1|4944557_4946453_-|hypothetical-protein	gnl|CDD|377924	pfam07833, Cu_amine_oxidN1, Copper amine oxidase N-terminal domain. Copper amine oxidases catalyze the oxidative deamination of primary amines to the corresponding aldehydes, while reducing molecular oxygen to hydrogen peroxide. These enzymes are dimers of identical subunits, each comprising four domains. The N-terminal domain, which is absent in some amine oxidases, consists of a five-stranded antiparallel beta sheet twisted around an alpha helix. The D1 domains from the two subunits comprise the 'stalk' of the mushroom-shaped dimer, and interact with each other but do not pack tightly against each other.	9.82687e-18
NZ_CP045293.1|WP_152395470.1|4927515_4928103_-|SIS-domain-containing-protein	gnl|CDD|184408	PRK13937, PRK13937, phosphoheptose isomerase; Provisional.	9.65907e-104
NZ_CP045293.1|WP_152395481.1|4948793_4949891_+|amino-acid-aldolase	gnl|CDD|143494	cd06820, PLPDE_III_LS_D-TA_like, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzymes, Low Specificity D-Threonine Aldolase-like. This subfamily is composed of uncharacterized bacterial proteins with similarity to low specificity D-threonine aldolase (D-TA), which is a fold type III PLP-dependent enzyme that catalyzes the interconversion between D-threonine/D-allo-threonine and glycine plus acetaldehyde. Both PLP and divalent cations (eg. Mn2+) are required for catalytic activity. Low specificity D-TAs show similarity to bacterial alanine racemase (AR), which contains an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain. AR exists as homodimers with active sites that lie at the interface between the TIM barrel domain of one subunit and the beta-sandwich domain of the other subunit. Based on its similarity to AR, it is possible that low specificity D-TAs also form dimers in solution. Experimental data show that the monomeric form of low specificity D-TAs exhibit full catalytic activity.	1.88802e-128
NZ_CP045293.1|WP_152395473.1|4930190_4931045_-|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|212494	cd08946, SDR_e, extended (e) SDRs. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	3.05049e-20
NZ_CP045293.1|WP_152397379.1|4934423_4935689_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|213187	cd03220, ABC_KpsT_Wzt, ATP-binding cassette component of polysaccharide transport system. The KpsT/Wzt ABC transporter subfamily is involved in extracellular polysaccharide export. Among the variety of membrane-linked or extracellular polysaccharides excreted by bacteria, only capsular polysaccharides, lipopolysaccharides, and teichoic acids have been shown to be exported by ABC transporters. A typical system is made of a conserved integral membrane and an ABC. In addition to these proteins, capsular polysaccharide exporter systems require two 'accessory' proteins to perform their function: a periplasmic (E.coli) or a lipid-anchored outer membrane protein called OMA (Neisseria meningitidis and Haemophilus influenza) and a cytoplasmic membrane protein MPA2.	8.08363e-111
NZ_CP045293.1|WP_152395469.1|4926818_4927514_-|NTP-transferase-domain-containing-protein	gnl|CDD|133065	cd06915, NTP_transferase_WcbM_like, WcbM_like is a subfamily of nucleotidyl transferases. WcbM protein of Burkholderia mallei is involved in the biosynthesis, export or translocation of capsule. It is a subfamily of nucleotidyl transferases that transfer nucleotides onto phosphosugars.	9.28841e-100
NZ_CP045293.1|WP_152397380.1|4946473_4947622_-|trypsin-like-serine-protease	gnl|CDD|273938	TIGR02037, Probable_periplasmic_serine_protease_do/HhoA-like, periplasmic serine protease, Do/DeqQ family. This family consists of a set proteins various designated DegP, heat shock protein HtrA, and protease DO. The ortholog in Pseudomonas aeruginosa is designated MucD and is found in an operon that controls mucoid phenotype. This family also includes the DegQ (HhoA) paralog in E. coli which can rescue a DegP mutant, but not the smaller DegS paralog, which cannot. Members of this family are located in the periplasm and have separable functions as both protease and chaperone. Members have a trypsin domain and two copies of a PDZ domain. This protein protects bacteria from thermal and other stresses and may be important for the survival of bacterial pathogens.// The chaperone function is dominant at low temperatures, whereas the proteolytic activity is turned on at elevated temperatures. [Protein fate, Protein folding and stabilization, Protein fate, Degradation of proteins, peptides, and glycopeptides].	4.51664e-65
NZ_CP045293.1|WP_152395476.1|4936647_4939116_+|O-antigen-ligase-domain-containing-protein	gnl|CDD|377422	pfam04932, Wzy_C, O-Antigen ligase. This group of bacterial proteins is involved in the synthesis of O-antigen, a lipopolysaccharide found in the outer membrane in gram-negative bacteria. This family includes O-antigen ligases such as E. coli RfaL.	7.29137e-06
NZ_CP045293.1|WP_152395472.1|4929144_4930161_-|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|187570	cd05260, GDP_MD_SDR_e, GDP-mannose 4,6 dehydratase, extended (e) SDRs. GDP-mannose 4,6 dehydratase, a homodimeric SDR, catalyzes the NADP(H)-dependent conversion of GDP-(D)-mannose to GDP-4-keto, 6-deoxy-(D)-mannose in the fucose biosynthesis pathway. These proteins have the canonical active site triad and NAD-binding pattern, however the active site Asn is often missing and may be substituted with Asp. A Glu residue has been identified as an important active site base. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	2.41821e-153
NZ_CP045293.1|WP_152395468.1|4926337_4926826_-|D-glycero-beta-D-manno-heptose-1,7-bisphosphate-7-phosphatase	gnl|CDD|319806	cd07503, HAD_HisB-N, histidinol phosphate phosphatase and related phosphatases. This family includes the N-terminal domain of the Escherichia coli bifunctional enzyme histidinol-phosphate phosphatase/imidazole-glycerol-phosphate dehydratase, HisB. The N-terminal histidinol-phosphate phosphatase domain catalyzes the dephosphorylation of histidinol phosphate, the eight step of L-histidine biosynthesis. This family also includes Escherichia coli GmhB phosphatase which is highly specific for D-glycero-D-manno-heptose-1,7-bisphosphate, it removes the C(7)phosphate and not the C(1)phosphate, and this is the third essential step of lipopolysaccharide heptose biosynthesis. This family belongs to the haloacid dehalogenase-like (HAD) hydrolases, a large superfamily of diverse enzymes that catalyze carbon or phosphoryl group transfer reactions on a range of substrates, using an active site aspartate in nucleophilic catalysis. Members of this superfamily include 2-L-haloalkanoic acid dehalogenase, azetidine hydrolase, phosphonoacetaldehyde hydrolase, phosphoserine phosphatase, phosphomannomutase, P-type ATPases and many others. HAD hydrolases are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	7.6285e-70
NZ_CP045293.1|WP_152395475.1|4935704_4936499_-|ABC-transporter-permease	gnl|CDD|224596	COG1682, TagG, ABC-type polysaccharide/polyol phosphate export systems, permease component [Carbohydrate transport and metabolism / Cell envelope biogenesis, outer membrane].	3.68537e-46
NZ_CP045293.1|WP_152395471.1|4928103_4929132_-|dehydrogenase	gnl|CDD|225325	COG2605, COG2605, Predicted kinase related to galactokinase and mevalonate kinase [General function prediction only].	2.70297e-135

Protein sequences

>NZ_CP045293.1|WP_152395473.1|4930190_4931045_-|NAD-dependent-epimerase/dehydratase-family-protein
MSIFIIGKSGYIAKRLIDYLDSNPIDNQDINVTSSHTEEQAMYLNLLEPQSFDYSMIKENDFIVLLAAISSPDICNRDYDTAYEINVSGTAYFISKCIERNARVLFMSSDTVYGLQQSEVDENTDTNPIGNYALMKQEIEQKFMGYSNFKVFRLSYIFSREDKFTSYIHGCCRKGEVVDVFHPIFRRTVYIEDLIQAIITIEQDWDEWSNQIFNICGPSLLSRVDLVQFYKFNVNNELEYRTTEPDESFFKARPKTIDMASIFFEKLLKRKPIKIDEAMSREFS
>NZ_CP045293.1|WP_152395472.1|4929144_4930161_-|NAD-dependent-epimerase/dehydratase-family-protein
MSKKRALITGITGMVGSHLVDYLLENTDWEVYGMCRWRSPFDNVQHLLPRINQRDRVHILYGDLNDYLSLHEVIEKSKPDYVFHLAAQSFPKTSFDAPIDTFNVNILGTARLLEALRKFNDIDPVIHVCASSEVFGRVPKEKLPIDEECSFHPASPYAISKIGTDLIGRYHAEAYGQKVMTTRMFTHTGPRRGDVFAESTFAKQIAMIEAGMIPPIVKTGNLDSLRTWADVRDAVRAYYMLVTVNPIAGEYYNIGGTYTCSVRDMLNTLVSMSSVKDIKIETDPERIRPIDADLQVPNTSKFKNHTGWAPEIPFETTMEDLLNYWRDRIKMGQNFLTR
>NZ_CP045293.1|WP_152395471.1|4928103_4929132_-|dehydrogenase
MLIRSKAPLRLGLAGGGTDVSPYCDEFGGYVLNATIDMYAYCTIEPTSDNKISFYATDREEYTEYDSTYFLEFDGVLDLHKGIYNRIIKQYHQSVPLSFRMTTYSDAPAGSGLGSSSTMVVAILHAFAEWLNLPLGEYDVAQLAYQIERQDVGLSGGKQDQYAATFGGINFIEFYNDDRVIVNPLRVKSWIVNELENSLVLYYTGASRESAKIIDEQVKNTTGKNMKSIEAMHELKIDALVMKEMVLKGDLRTFANYLGKSWEAKKRTASTITNQSIDRVYDIAIASGAYAGKVSGAGGGGFMMFMVDPAKRINLIKELQRLDGVVMNFHFTKNGAESWRIN
>NZ_CP045293.1|WP_152395470.1|4927515_4928103_-|SIS-domain-containing-protein
MQSFINNQIKESYEIKRLILESTELTKLIKEVAEKTTVVYRNGKKTLLAGNGGSAADAQHIAGEFVSRFYFDRPGIPSVALTTDTSILTAIGNDYGYERLFARQIQAQGSEGDLFIGISTSGNSPNIISALKECREKGIITVGLTGASGGRMEEFCDYCIKVPSDETPRIQESHILIGHIICAVVEESIFGKGFN
>NZ_CP045293.1|WP_152395469.1|4926818_4927514_-|NTP-transferase-domain-containing-protein
MEAIILAGGFGTRLQSAVNDVPKPMAPINGQPFLTYLLKYLLKYDIRSVLLSTGYKHEVIEDYYGSCFQGVMRLEYSVEKEPLGTGGAIAQSMRYTTEEDIIVINGDTFFNVDLKEMMLFHRTQAGEMTMALKPMSDFERYGKVDHVNNRVVKFQEKQYTSFGDINGGVYILNRSIFNGCNLEKTFSFETDFLQKHLQRIQVNSYIADEYFIDIGIPEDYYKAQSELIKFE
>NZ_CP045293.1|WP_152395468.1|4926337_4926826_-|D-glycero-beta-D-manno-heptose-1,7-bisphosphate-7-phosphatase
MNKAVFFDRDGVINVEKNYVYKIEDFEFVDGIFDVMKHFQSLGYLLIVITNQAGIGRGYYSEEDFHKLNDWMIERFKVEGIEITKVYYSPYHPEHGIGEYKKDSWCRKPNPGMILQAKDDFDIDLRESILFGDKDSDIEAGIRAEVGENVLVQMNVKINANK
>NZ_CP045293.1|WP_152395467.1|4924292_4925657_-|hypothetical-protein
MHFHLIHEKKKKKKIIAFGLIVSPIIFYLMFKKLFLKSSILVGTGYTSIKINVYSVIKFFIGGLLNLFGFNIGPEHLNGIPINQVNLTTIIVSVLVLILSMIVFIAAIKGKDKKEKLIEFKIFLIMLMLVCALVLVSSITVYQELRWLQTPYLVFIIYMGYLFAKINSKKLMMILMILFTCCNLKQNSYYKDYIHNIYFVYSQQISDSAYDETIKKYGTNIRQYKVFIEKHRDIDWPLLDSLFLKPYLGDDTFKVEYVDNILDVDLTKIDPTKVVLLKLNDSQKRFINVTNEVILYKNKALGKNKNIKYSLIDHFHEGEVTPQSVNEDTPNGEGVFIFDWTTQFQKINTLTIISGFKYTYKNIFIPTDSKICGDLILPLKGSDGANFYISINDNGNERRIYESNVTQESNFNEIEISIEGYSGKNVDITFGVESPNGNNIADWIALGDLGIAQR
>NZ_CP045293.1|WP_152395466.1|4922540_4924151_-|lipopolysaccharide-biosynthesis-protein-RfbH
MLIIDAEEYLKYLKECRHLKQGSIVKFKNTGEYGLIGYELENIFQVFKLSKNAPEIQNGNFHEVIKVNKETPLFLDVRDKLHVLKNDIEFIFDLSEHDFEKVMRLEILSKVENYYDLFHSNRNKKFDVEKSSLSYGGRIYDEKEMRSLVDSSLDFWLTAGRYNKQFEKEFAEFLGVRYALLTNSGSSANLLAFSTLTSPKLGDRRVMPGDEVITVAAGFPTTVAPIIQNGAIPVFIDVELGTYNIMVDRIEDAITPRTKAIMVAHTMGNPFELDKVMEIAEKYNLWVIEDNCDALGSTFNGKLTGTHGHIGTSSFYPPHHMTMGEGGAVYTNDPKLKMIIESFRDWGRDCWCESGCDNTCKKRFGWELGSLPYGYDHKYTYSHIGYNLRVTDMQAAIGVEQLKKVPSFVQARKNNFNRLLAGLRELDQYFILPRATENSDPSWFGFILTLRDGVNFTKNEIVDYLEANRIQTRMLFAGNLIRQPAYQNVNFRIHGGLKNTDKILYDTFLVGVYPGLSDEMIDYVIDKIKEFVYSKN
>NZ_CP045293.1|WP_152395465.1|4921715_4922510_-|glucose-1-phosphate-cytidylyltransferase
MKVVILAGGYGTRISEESHLKPKPMIEIGQKPILWHIMKLYSQHGFNDFVICLGYKGFYIKEYFAHYFLHESDVTFDFRNDNQIITHNHSAEPWKVTLVNTGLDTMTGGRVKRIQPYIEDEPFMLTYGDGVSDVNITELVNYHKLHGRIGTVTSVQPSGRFGALNITENNLVKGFQEKPKGDNSWINAGFFVLQPEIFNYIADDSTIFEKAPLETLAKNEELMSYKHDGFWQPMDTLRDKNYLEDLWGSGKAPWKTWDRDPVNV
>NZ_CP045293.1|WP_152395464.1|4920654_4921719_-|CDP-glucose-4,6-dehydratase
MINTNFWVNKRVFITGHTGFKGSWLSLWLHSMGAKVYGYAQIPNTEPSLYHVCGIDEILEKSFIADIRDSKSLQEAMEFSSPEIVIHMAAQPLVRESYINPVDTYSINVMGTVNLFEAVRNCSSVKAVVNVTTDKCYENKEWVWGYRENEPMGGYDPYSSSKACSELVTSAYKNSFFYHNEKRFVGVASARAGNVIGGGDWAKDRLIPDCIKALMADQTIIIRNPYSIRPWQHVLEPLGGYLLLAEKLFEDGEKYSEAWNFGPYDIDAKPVEWIVQEMCNKWGTEANYRVDSNPQPHEAQYLKLDCSKANAILNWSPRWNLETAIEKIVSWTKAYRNNENMREVCIKHIKEYQS
>NZ_CP045293.1|WP_152397379.1|4934423_4935689_-|ATP-binding-cassette-domain-containing-protein
MTSNYALKVENISKIYKIYDKPSDRLKEALIPFGKKFYTDFHALNGISFKVSKGESLGILGKNGSGKSTLLKIITGVLTQTTGTIQVNGRISALLELGAGFNPEYTGIENIYLNGTIMGFSKEAMDAKIKDILDFADIGDFIYQPVKMYSSGMFARLAFAVAINVDPDILIVDEALSVGDMRFQQKCYRKIEEFKDTKTVIMVTHDISAITKYCDRAIWINEGNLMGDGSPIEIAKKYQAFMIDSAISKNDSKSSLGFEKDDNIDAINPSLDVMGDRSVEIVGISMFDELSSTKLDLVAPDQRIKISIKVKSNQNITDPIVGLSVKDRLGTTLFQTNSFVLNQPMDDLHDNEMAIYSFSFYFPSLNHGMYTISPAIASGTQGNHTQHCWIHDAIVFHVIQKQIFELEGCLVMNNIDFSRNL
>NZ_CP045293.1|WP_152395475.1|4935704_4936499_-|ABC-transporter-permease
MITGFLKDVFIKQKFILEMSKKDIKSRYLGSFLGVVWAFIQPTVQILIFWFVFQVGFKSAPVDNFPFILWLISAMIPWFFISDSIIGATNSIIDNSYLVKKIVFRVSILPIVRIYSALFIHLFFICFMIIMFAVYGYLPTVYYLQIFYYLFASILLVLGISWITSSLVIFLKDIGQFVGVLVQFGFWLTPIFYSINTVPEKYHFLLKLNPAFYIVEGYRETFIYHKWFWEHPLLSLNFWIITILLLTAGTFIFKKLRPHFADVL
>NZ_CP045293.1|WP_152395476.1|4936647_4939116_+|O-antigen-ligase-domain-containing-protein
MSSFLNEEGDCRTMSYPSYGKIKNTTSKISKHDQTSLIQWILMGVLALFLLWSPLWAALFNGQQITFERPLYEAMRWVAVIMLITGVYLFKNWRPGDIKDWYAILVFALPLTYLISLIPAASHYQALNMVYVYLIYAIIFVVGLYFTRNARDNSIIRNTLLVSTYFTVFFGLFHWFGNSKFIADVLGWLIPLKSAAGTYLDAVMTDSNGLRLTSFFQYANTYAAFLIAILFASAFLLVKSRKWYVSAIHAFMLVPIILSFFLTLSRAAYVILPVVFLIVILCLKPYRQIMYTVHMAIAFIASMAILNKVTTIGISVNEQFNGSESLKGWMLTLGVSLAVAILATLSQQFVTPWLQQKLNQFGQRKASSLIMPAAAVILGVVMVFVFIGTSAKNLLPENVKIRLENINFNQHSVLERGTFYKDAMKLVADYPVFGAGGGAWYSMYEKYQHNPYISRQAHSFFFQNIVEVGIVGFSVLVGLLILFFYTYLKNFVRSEENDRDSHFYYFIIAIALLIHSALDFDLSYVYVGVLLFLCLGAMLANIKSQESVKLKKLTGLKWAYPSFISVLALVMFIFAQMSLSANASFMTSLTMVQQQTSNDYNQIVTPLNKALGLRENPDYTQLKVQLLQSVYSQNQNQPFYDEAQSLLDKTLKKEPYNFGLISLQMKQYDLIGDKKKQLTLVEEQLKNFPWNMTLYENAIQLNINSENYDAALATYQKILDQKQVLASLPKEQSQGRAFDITPKTNLDIAKIYFTQANYEKASAFIKPLLTADYNDAVNKDMARYYVISLQKQGTTDQAVYDALVATGVNEKDIIDAIAADAK
>NZ_CP045293.1|WP_152395477.1|4940453_4941323_-|UTP--glucose-1-phosphate-uridylyltransferase-GalU
MKIRKAIIPAAGLGTRFLPATKAMPKEMLPIVDTPTIQYIVEEAVASGIEDIIIVTGKSKRAIEDHFDNSFELEHTLLEKGKIQLLGEVQKSSQMADIHYIRQKEPKGLGHAVWCARKFIGNEPFAVLLGDDIVQSGDPCLKQMIEVFNQHQASVVGVQPVPHAEVSRYGIVDGLAIGERLYQAKGFVEKPPVDQAPSDLAIMGRYILTPAIFDILDQQDVGAGGEIQLTDAIARLNQQERVLAYHFLGKRHDVGEKLGFIKTTIEYALQKEELRDELREFMRGIVETK
>NZ_CP045293.1|WP_152395478.1|4941449_4944074_-|U32-family-peptidase
MSQTTLTRADIELLAPAGDWDCMRAAVANGADAIFFGVEKFNARARANNFQMDELPEIMAFLHSYGVKGFLTFNILVFEEELPDAKELIDACIDAGVDAVIVQDLGLVKMIREISPDFPIHGSTQMTITSPEAVEFTKPWDMERVVLGRENNLKQIKMIGDQAKLPMEVFVHGALCVSYSGQCLTSEMWGGRSANRGECAQACRLPYDLMVDGEQKPMGDVAYLLSPKDLAAIDIVPELIEAGVTSFKIEGRLKSPEYVANVVSKYRKAIDQYFAGDRSGPSKEEIRELQQSFSRGFTHGFLEGTNNKKLVEGTFPKSRGVYLGRVEKILRDGVVCKIEAPLKRGDGIVFDAGDPTKKEEGGRVYDVRRQGVKLEGEAAEGWIIDIVPGRNDVNLQKVHVGDRIWKTSDPALDKRLRQTFETEKPYRVFPVHVRVEGRAGEPLRTWWTDVQKGVTVQVDSELLLEEALKRPMDAALLEEQLGRLGGTLFQLEAMDAHLEGAVILPMRELNALRRSAVEQLAGERPKPPVYVKRAVEVYADAKAHAPGTVHSKLTALCRTLEQVQAAAASEVGMIYADFEFIKQFPAAVEAARAAGKQIALVTPRIHMPNENGYHRNILKLQPDAILVRNTGALYFYMRARAEFEAMKNGMNVNAVASGDILHVGTAVGPSNISTGSLADTFAKMEKFPRLIGDFSLNIANHKAADLFVEAGCDLVTPSYDLNIQQMVDLLGRADTSKMEVVIHQHLPMFHTEHCVYCTFMSEGTDYTNCGRPCEEHRASLQDRIGMSHPVRVDEGCRNTVYNAIEQSGAEYIQNFLELGVTHYRVEFLEETADQVHEVIDLYSRALQGKISGTKVWKTLKATNQLGVTRGQLVK
>NZ_CP045293.1|WP_152395479.1|4944557_4946453_-|hypothetical-protein
MGKKLSGWLICLVLAFTMVMPGVAMAGAGDSVELKFKLGSTNATLNGQRISIAKPYTEKGTTMVPLSLITKAFQVEFSFENNKKITITSGDHTIQFVIGSTNATVDGRTVPTGAAPQLVNGVVMVPMRVVTDALAANVKVDADHTIVITANLDGNAGTGAIGGIDSDAGKTMIGDSYYSWSMRYPTGLVKQFQSEADDYVSFTDEKGTYLLAVSVSKVDDKMTDDDLLKQLTNAALSENGLVVDKKTVKSGTTPYAQVISKGEDGVYSAIRGYYANDTYYELYYSDGLAKNYKDLAKHNDLLNSFRPAYDKGNAKLKDLSTVVGGMRKVVNSDYGVTVNVPASWELYPEDLIFGNDDGTAQLTFDISSAASGLKLDAWAGQMDQYFKDVFVPDAWKLLTTEPIKVDGQEGLLKKYQFTTGEDTYVQSEIFLIAGSYKYLIQYDYDAKNKAADSLFGTLVKGIKLNTKELSSNFGFLEDTRAYVDRSLTTVKSSKKNAYSLTIPNYWTRIESEYGASDPGKVQYHFPGGSFEVSVNPSDRTLSEEVEAYKYVYEQQRILYKNYTVTSTDSTTLAGQPAYKIVLDGKEAHYEQYVIVKNGKVYSLLSTVMKANRTDVNEKAIQSVFQSLKWTN
>NZ_CP045293.1|WP_152397380.1|4946473_4947622_-|trypsin-like-serine-protease
MSGMKSGNRARMRRMVCGSAIALMVFSNAAGVLAAGQSSDAQLEAKVVDGQVYVKASSLVSQLGGQGVYDAKSQTYQYKSGNSVPSIVKKLSPSVVAIIGKVSEGGEVDTSDRYNLAHGTGVVLKKDGWIVTNAHVVSGLKNAVVVMSDGKSYTIVKQFVDEVSDIAIIQINAKNLTPAVFAPSTASVEVGESVVALGTPISFSFRNSATVGVISGLNRSVDSIYKLIQTDAAINPGNSGGPLVNMKGEVVGINSLKYSAIGVENMGFSIPTNTVQYIVNQLMQYGKVKRPALGFDMEESWSAIVGLPTNEPLTVTRVDSDAAAKAGVKAGDVLYSINGKQVTTMLDINEMFKGYMPGQTVKLMMQSGGDLVERKLQLTEQS
>NZ_CP045293.1|WP_152395480.1|4948060_4948702_+|transcriptional-regulator
MERIEAEFEFLSSLVRGIAAQFGENCEVVLHDLTRPYDSTIVAIENGHVTGRKVGDPGTNLGLELLRGQSDSGNKINYVTQTKDGRILRSTSLYMRNSEGTVIGSLCINYDITDLMMAEKTLQSLTASGLQPEVRESFVSNVSDLLDQLIQEAQEQVGRPVAAMTKEDKMRLIQLLDQKGAFLIKKAGEKICGYLNISKYTLYSYLEESKTSE
>NZ_CP045293.1|WP_152395481.1|4948793_4949891_+|amino-acid-aldolase
MSTHLETPCIVIDAAKVRQNIDRMAQTIQSHGVKLRPHAKTHKMPSVAQSQLEAGSHGITVAKVSEAEVMAAGGITDIFIAYPLVTPSKIARAIELSRSIRLIIAVDSLEGARRLSEQAAAAGTSLEVRLEINTGLRRTGVNPDQAVALGQQIDAFDHLRLTGIFTFRGALIDGAATLDLERAGRDEGEWMVRIATAMRDAGLTIEDVSVGSTPTAAYAAAVPGITEVRPGTYVYQDRMQAAFGVCAINDCAASVLVTVVSRPSPDLLVIDGGSKTFATDVQPGTAPLHLVGFGHVIGTPEAVLERLSEEHGMLRVPADCPWQVGDLIQIIPNHICSTVNLHNQVIWQDQGEWTAMPVLGRGMLE
>NZ_CP045293.1|WP_152395482.1|4949925_4951530_+|amidohydrolase-family-protein
MLDLMLKNGKIVDGTGNPWIAGDVGIKQGQIVQVGQLQQEAHRTIDVHGQVIAPGFIDGHCHSDLMILDHPYSEIKLQQGVTTEVVGNCGLAPAPFFPETASLLQTYVEPILGKTKWNWPWKTVEQYMETLAKSSPSENIATYVAHGALRIAVMGFANRPATREELDRMKQLLEEGLRAGAIGLSIGLLYAPGSYTSREEIAELCSVLPKYNGLFSTHIRGEGNNLLPSIEEVIWIAEKTGVSLHISHLKAAGRANWGKILEALELIEAARGRGMDVTVDVYPYNAGSTMLTTVLPPWVLEGGIERTLEAFRDPSIRRRVREELGSEQKDWDNLVYSTGWHSVYLSAVHTEANRPLEGKHIEEISELRGQHPVDCVMDLLLEEGGQISIVYFHMSDSDVKEVIRYDKSLIASDSLTCETGKPHPRLYGSFPRIFAKYVREEKTLTLEQAVRKMTSFPVQRFKLGKRGLIVPGYIADLVVFDPATITDTATYQDPRQYPTGISEVIVRGEPTLSHGRHTRAREGAFIPAQHCCHH

Crispr_ID: NZ_CP045293_7

• CRISPR_ID: NZ_CP045293_7
• CRISPR_location: 5397427-5397704
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 5 spacers

Consensus repeat of NZ_CP045293_7

Consensus_repeat	Method
AAATAACTGCTAAAAAGCATTTA	CRISPRCasFinder
GCAAAATAACTGCTAAAAAGCATTTA	PILER-CR

spacers of NZ_CP045293_7

>7.1|5397450|28|NZ_CP045293|CRISPRCasFinder
TTTGGTGGAAATGTGATCTGAAAATACG
>7.2|5397501|28|NZ_CP045293|CRISPRCasFinder
ATTTGGAGAAAAAGTGGGCGTGCTCACA
>7.3|5397552|29|NZ_CP045293|CRISPRCasFinder
ATTCGGAGAAAAAGTAGGCCAACCTCGCA
>7.4|5397604|28|NZ_CP045293|CRISPRCasFinder
ATTAGCTGGAAAGTCGCTCGAGAATACG
>7.5|5397655|27|NZ_CP045293|CRISPRCasFinder
ATAGCCGGAATAAGGTTTGAAACTGAA
>7.6|5397604|29|NZ_CP045293|PILER-CR
GCAAATTAGCTGGAAAGTCGCTCGAGAAT
>7.7|5397659|24|NZ_CP045293|PILER-CR
ATAGCCGGAATAAGGTTTGAAACT

CRISPR arrays and Neighbor proteins around NZ_CP045293_7

CRISPR arrays

The CRISPR arrays of NZ_CP045293_7

>merge|NZ_CP045293|7|5397427-5397704|CRISPRCasFinder,PILER-CR
GAATACTTGCTAAAAAGCATCTATTTGGTGGAAATGTGATCTGAAAATACGAAATAACTGCTAAAAAGCAGTTAATTTGGAGAAAAAGTGGGCGTGCTCACAAAATAACTGCAAAAAGGCAGTTAATTCGGAGAAAAAGTAGGCCAACCTCGCAAAATAACTGCAAAAAAGCAGCAAATTAGCTGGAAAGTCGCTCGAGAATACGAAATAACTGCTAAAAAGCATTTAATAGCCGGAATAAGGTTTGAAACTGAAAAATAACTGCTAAAAAGCATTTA

>NZ_CP045293|7|5|5397427-5397704|CRISPRCasFinder
GAATACTTGCTAAAAAGCATCTA	TTTGGTGGAAATGTGATCTGAAAATACG
AAATAACTGCTAAAAAGCAGTTA	ATTTGGAGAAAAAGTGGGCGTGCTCACA
AAATAACTGCAAAAAGGCAGTTA	ATTCGGAGAAAAAGTAGGCCAACCTCGCA
AAATAACTGCAAAAAAGCAGCAA	ATTAGCTGGAAAGTCGCTCGAGAATACG
AAATAACTGCTAAAAAGCATTTA	ATAGCCGGAATAAGGTTTGAAACTGAA
AAATAACTGCTAAAAAGCATTTA

>NZ_CP045293|7|1|5397578-5397704|PILER-CR
GCAAAATAACTGCAAAAAAGCAGCAA	ATTAGCTGGAAAGTCGCTCGAGAATACGA
AATAACTGCTAAAAAGCATTTAATAG	CCGGAATAAGGTTTGAAACTGAAA
AATAACTGCTAAAAAGCATTTA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045293.1|WP_152395827.1|5399615_5399879_+|DUF1450-domain-containing-protein	unknown	unknown	gnl|CDD|377806
NZ_CP045293.1|WP_152395826.1|5398743_5399238_+|single-stranded-DNA-binding-protein	unknown	unknown	gnl|CDD|180915
NZ_CP045293.1|WP_152395828.1|5400062_5400869_+|TIM-barrel-protein	unknown	unknown	gnl|CDD|366542
NZ_CP045293.1|WP_152395825.1|5398412_5398700_+|30S-ribosomal-protein-S6	unknown	unknown	gnl|CDD|179034
NZ_CP045293.1|WP_152395830.1|5403073_5403988_+|DUF2232-domain-containing-protein	unknown	unknown	gnl|CDD|370773
NZ_CP045293.1|WP_152395817.1|5390218_5390470_+|DUF3343-domain-containing-protein	unknown	unknown	gnl|CDD|378728
NZ_CP045293.1|WP_152395819.1|5391412_5391628_+|DUF951-family-protein	unknown	unknown	gnl|CDD|377606
NZ_CP045293.1|WP_152395823.1|5394999_5395581_+|TetR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP045293.1|WP_152395824.1|5398001_5398196_-|YjzC-family-protein	unknown	unknown	gnl|CDD|372942
NZ_CP045293.1|WP_152395821.1|5393298_5393964_-|HAD-hydrolase-like-protein	unknown	unknown	gnl|CDD|136007
NZ_CP045293.1|WP_152395815.1|5389033_5389528_+|DUF4446-family-protein	unknown	unknown	gnl|CDD|379655
NZ_CP045293.1|WP_152395822.1|5394250_5394835_+|cell-wall-associated-hydrolase	unknown	unknown	gnl|CDD|366353
NZ_CP045293.1|WP_152397412.1|5395629_5397084_+|DHA2-family-efflux-MFS-transporter-permease-subunit	unknown	unknown	gnl|CDD|129794
NZ_CP045293.1|WP_152395829.1|5402112_5402529_+|CBS-domain-containing-protein	unknown	unknown	gnl|CDD|341404
NZ_CP045293.1|WP_018754181.1|5402756_5403068_+|hypothetical-protein	unknown	unknown	gnl|CDD|378899
NZ_CP045293.1|WP_152395820.1|5391999_5393256_+|hypothetical-protein	unknown	unknown	gnl|CDD|376461
NZ_CP045293.1|WP_152395816.1|5389502_5390108_-|spore-protease-YyaC	unknown	unknown	gnl|CDD|131888
NZ_CP045293.1|WP_078498027.1|5399258_5399540_+|30S-ribosomal-protein-S18	unknown	unknown	gnl|CDD|178997
NZ_CP045293.1|WP_152397413.1|5401094_5402066_+|LytR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224235
NZ_CP045293.1|WP_152395818.1|5390494_5391409_+|mechanosensitive-ion-channel	unknown	unknown	gnl|CDD|223740

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045293.1|WP_152395827.1|5399615_5399879_+|DUF1450-domain-containing-protein	gnl|CDD|377806	pfam07293, DUF1450, Protein of unknown function (DUF1450). This family consists of several hypothetical bacterial proteins of around 80 residues in length. Members of this family contain four highly conserved cysteine residues. The function of this family is unknown.	3.02684e-07
NZ_CP045293.1|WP_152395826.1|5398743_5399238_+|single-stranded-DNA-binding-protein	gnl|CDD|180915	PRK07275, PRK07275, single-stranded DNA-binding protein; Provisional.	4.11343e-59
NZ_CP045293.1|WP_152395828.1|5400062_5400869_+|TIM-barrel-protein	gnl|CDD|366542	pfam01261, AP_endonuc_2, Xylose isomerase-like TIM barrel. This TIM alpha/beta barrel structure is found in xylose isomerase and in endonuclease IV (EC:3.1.21.2). This domain is also found in the N termini of bacterial myo-inositol catabolism proteins. These are involved in the myo-inositol catabolism pathway, and is required for growth on myo-inositol in Rhizobium leguminosarum bv. viciae.	4.7454e-09
NZ_CP045293.1|WP_152395825.1|5398412_5398700_+|30S-ribosomal-protein-S6	gnl|CDD|179034	PRK00453, rpsF, 30S ribosomal protein S6; Reviewed.	2.66534e-42
NZ_CP045293.1|WP_152395830.1|5403073_5403988_+|DUF2232-domain-containing-protein	gnl|CDD|370773	pfam09991, DUF2232, Predicted membrane protein (DUF2232). This family of bacterial proteins are multi-pass membrane proteins with up to 10 (2 x 4/5) transmembrane regions. The exact function of this potential pore molecule is not known, but in many instances it is associated with ABC-transporter-like domains, implying that it is part of a secretion system that uses energy.	6.37385e-28
NZ_CP045293.1|WP_152395817.1|5390218_5390470_+|DUF3343-domain-containing-protein	gnl|CDD|378728	pfam11823, DUF3343, Protein of unknown function (DUF3343). This family of proteins are functionally uncharacterized. This protein is found in bacteria and archaea. Proteins in this family are typically between 78 to 102 amino acids in length.	5.75722e-17
NZ_CP045293.1|WP_152395819.1|5391412_5391628_+|DUF951-family-protein	gnl|CDD|377606	pfam06107, DUF951, Bacterial protein of unknown function (DUF951). This family consists of several short hypothetical bacterial proteins of unknown function. Structural modelling suggests this domain may bind nucleic acids.	4.82812e-29
NZ_CP045293.1|WP_152395823.1|5394999_5395581_+|TetR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	2.042e-16
NZ_CP045293.1|WP_152395824.1|5398001_5398196_-|YjzC-family-protein	gnl|CDD|372942	pfam14168, YjzC, YjzC-like protein. The YjzC-like protein family includes the B. subtilis YjzC protein, which is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are approximately 60 amino acids in length.	1.97672e-24
NZ_CP045293.1|WP_152395821.1|5393298_5393964_-|HAD-hydrolase-like-protein	gnl|CDD|136007	PRK06698, PRK06698, bifunctional 5'-methylthioadenosine/S-adenosylhomocysteine nucleosidase/phosphatase; Validated.	5.87596e-35
NZ_CP045293.1|WP_152395815.1|5389033_5389528_+|DUF4446-family-protein	gnl|CDD|379655	pfam14584, DUF4446, Protein of unknown function (DUF4446). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria and eukaryotes. Proteins in this family are typically between 165 and 176 amino acids in length.	1.71273e-57
NZ_CP045293.1|WP_152395822.1|5394250_5394835_+|cell-wall-associated-hydrolase	gnl|CDD|366353	pfam00877, NLPC_P60, NlpC/P60 family. The function of this domain is unknown. It is found in several lipoproteins.	4.23067e-29
NZ_CP045293.1|WP_152397412.1|5395629_5397084_+|DHA2-family-efflux-MFS-transporter-permease-subunit	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	5.6852e-83
NZ_CP045293.1|WP_152395829.1|5402112_5402529_+|CBS-domain-containing-protein	gnl|CDD|341404	cd09834, CBS_pair_bac, Two tandem repeats of the cystathionine beta-synthase (CBS pair) domains present in bacteria. The CBS domain, named after human CBS, is a small domain originally identified in cystathionine beta-synthase and is subsequently found in a wide range of different proteins. CBS domains usually occur in tandem repeats. They associate to form a so-called Bateman domain or a CBS pair based on crystallographic studies in bacteria. The CBS pair was used as a basis for this cd hierarchy since the human CBS proteins can adopt the typical core structure and form an intramolecular CBS pair. The interface between the two CBS domains forms a cleft that is a potential ligand binding site. The CBS pair coexists with a variety of other functional domains and this has been used to help in its classification here. It has been proposed that the CBS domain may play a regulatory role, although its exact function is unknown. Mutations of conserved residues within this domain are associated with a variety of human hereditary diseases, including congenital myotonia, idiopathic generalized epilepsy, hypercalciuric nephrolithiasis, and classic Bartter syndrome (CLC chloride channel family members), Wolff-Parkinson-White syndrome (gamma 2 subunit of AMP-activated protein kinase), retinitis pigmentosa (IMP dehydrogenase-1), and homocystinuria (cystathionine beta-synthase).	8.10902e-67
NZ_CP045293.1|WP_018754181.1|5402756_5403068_+|hypothetical-protein	gnl|CDD|378899	pfam12643, MazG-like, MazG-like family. This family of short proteins are distantly related to the MazG enzyme. This suggests that these proteins are enzymes that catalyze a related reaction.	1.27573e-21
NZ_CP045293.1|WP_152395820.1|5391999_5393256_+|hypothetical-protein	gnl|CDD|376461	pfam01120, Alpha_L_fucos, Alpha-L-fucosidase.	1.64038e-49
NZ_CP045293.1|WP_152395816.1|5389502_5390108_-|spore-protease-YyaC	gnl|CDD|131888	TIGR02841, Uncharacterized_protein_YyaC, putative sporulation protein YyaC. A comparative genome analysis of all sequenced genomes of shows a number of proteins conserved strictly among the endospore-forming subset of the Firmicutes. This protein, also called YyaC, is a member of that panel and is otherwise uncharacterized. The second round of PSI-BLAST shows many similarities to the germination protease GPR, which is found in exactly the same set of organisms and has a known role in the sporulation/germination process. [Cellular processes, Sporulation and germination].	1.95247e-76
NZ_CP045293.1|WP_078498027.1|5399258_5399540_+|30S-ribosomal-protein-S18	gnl|CDD|178997	PRK00391, rpsR, 30S ribosomal protein S18; Reviewed.	1.1677e-38
NZ_CP045293.1|WP_152397413.1|5401094_5402066_+|LytR-family-transcriptional-regulator	gnl|CDD|224235	COG1316, LytR, Transcriptional regulator [Transcription].	7.28734e-55
NZ_CP045293.1|WP_152395818.1|5390494_5391409_+|mechanosensitive-ion-channel	gnl|CDD|223740	COG0668, MscS, Small-conductance mechanosensitive channel [Cell envelope biogenesis, outer membrane].	7.33028e-41

Protein sequences

>NZ_CP045293.1|WP_152397412.1|5395629_5397084_+|DHA2-family-efflux-MFS-transporter-permease-subunit
MQATTQTEGKSYKVMPIMISLLISGFVGMFSETALNIALSQLMEILHITPATAQWLTTGFLLTLGILVPVSGLLLQWFTTRQLFVASLSFSIAGTLVAALAGNFEVLLIARVLQAVGTALLLPLMFNTILVIFPPEKRGAAMGVIGLVIMFAPAVGPTAAGLIIEHLTWNWIFWISLPFLVIGLLFGIAYMQNVSTVTKPKIDILSIILSTIGFGGIVFGFSKAGEEGWSNPIVLITIGAGIAALILFSIRQLTMKKPMMDLRVFKYPMFVVGTLMVLICMMIILSTVLILPLYMQNGMGLSAFTAGIALLPGGILNGLMSPVMGKLFDKYGPRWLVIPGLIIAGVCLWFFTSLTTTSAIALIIVLHSCLFIGISMVFMPAQTNGLNQLPPSMYPDGTAVMNTLQQVAGAIGTAVAVSILSHGTSDYLKTSANPQDPMEIVKGMTMGAQHSFLFGLIIAVVGLVLAFFIRRVHVEKQEMKVSMH
>NZ_CP045293.1|WP_152395823.1|5394999_5395581_+|TetR-family-transcriptional-regulator
MRVKPKTRDHIVEIATRLFFVQGYHATGLNQIIQESQAPKGSLYYYFPNGKEELAQVCIEQQRKHTAEILRSNFTASNDFVTGVQAFFLGLVQEIERQQFQGVPPSCFWNAVETSCISNRLREACQDTFDMWKSIMVERLLKEGHEEKRAESIAMGVFSLLEGSFVLALTYRDANPLINASNLIPLLLISESN
>NZ_CP045293.1|WP_152395822.1|5394250_5394835_+|cell-wall-associated-hydrolase
MKNPTNKRIHKTAVAMMLSLSITLSAGLIIPAPSAQAAPTTNSYTVAMAVMNTGEKFLGVPYKFSAEAGRTDQFDCSSFTQYVFKKNGIDLPRSSREQATVGTRVAKSDLRAGDLVFSDTNHDGIINHVSIYMGDGRLLHTYRVGIGVAISNFEGSTWDKTFVTARRVIPDNTNLTYDNNNSDNNNGNWDNQAE
>NZ_CP045293.1|WP_152395821.1|5393298_5393964_-|HAD-hydrolase-like-protein
MLQKPAAMIFDLDGTLFQTETIVIEAFHLTYAKLREENLYHGDVPADQDILGCLGMLLEHIWERLMPKASLEVRERANELMHEYENALMERGQGKLYPGVAETLQALRDQGIRLFVGSNGLEGYVKDVTRHMGIDHLFERLYSAGEFQTATKVDLIRILLENHQVPTAWMVGDRSSDIEAGKKNQITAIGCDYAGFRKSGELEGADAIITSFDELLHLIRS
>NZ_CP045293.1|WP_152395820.1|5391999_5393256_+|hypothetical-protein
MLSKTTVVPKVKQLQFQDWEYGLFLHFGLRTFYEGYVDFDERPMTPEVFMPTNLDCEQWIRNAKESGMEYAVLTAKHHDGFSNWPSKYTKFSVAYSPWKNGQGDVVREFVEACRKNDVKPGLYYSPFDGSADFYTQDAKAYDDYFVNQITELLGDYGDIDILWFDGCGSEGHEYDWPRIIREIRRLQPNILIFNIGDPDFRWIGNEDGIAPIPTWNVTDAIEWSILSEGEDELSGQHWLPAECDVQLRSTWFYSDQNEDTLKSLDELMGLYYHSVGRGTNLLLNIGPDREGLLPAIDVERVQQMGAEIRRRFGQPIADTSTFVEEKPGKWVYQTDKPHLIDHVVLQENLEQGERVRRFTVTVISKKTHKPVQVYEGINMGHKAIIRIPAVYIRGVIIEVTESEGTPILREASLHYTGA
>NZ_CP045293.1|WP_152395819.1|5391412_5391628_+|DUF951-family-protein
MERKQFELWDVVQMKKPHPCGTNEMEIIRMGMDIRVKCVGCQHSVLIPRQKFEKNMKKVLRNTKQITPPTE
>NZ_CP045293.1|WP_152395818.1|5390494_5391409_+|mechanosensitive-ion-channel
MAYYALAEETGEIIEQNLNWFQKKIWGPVTNPELWENMMWEIIKVLLIIIVCRVLIRVLHKAINHLIIKKGDTRLQFTPRRMITIGKLLKNVTTYVINFVMILMVISEWNIVDLRPVLAGAGVLGLAIGFGAQSLVKDIITGFFIIFEDQFAVGDVIEVNKNRGTVEVIGLRSTRIQSWTGEVFIIPNGMINEVTNFSLHNSVAFIDISVAYEENVDEAMEIMKKAMPELKERNLDIVKVPEVLGVQMMSASDVKIRIIAECKPYTQAGVARFINIEMKRLLDAHGIEIPYPRMVTYHRSEREG
>NZ_CP045293.1|WP_152395817.1|5390218_5390470_+|DUF3343-domain-containing-protein
MGTWMLIAFDSTQQALRTEMLLEFLDIEIDICPTPKEITAGCALSIHFPAQEVELVKKTIRDEQVEIRGIFRQQEHEYVFVDM
>NZ_CP045293.1|WP_152395816.1|5389502_5390108_-|spore-protease-YyaC
MSFSLYSSRIKELPSLKIAHTESHIHAAVTNRIVDFLTPIPAESTITVVCVGTDRSTGDCLGPLVGTALSKFNSPLFEIYGTLDHPVHAVNLSDTLQYIESSVKNPFIIGIDACLGQTTSVGNIQVASGPVRPGAGVHKQLPPVGDMHITGIVNVGGFMEYFVLQNTRLSLVMKLSDIIANSLYMAIKQWHHRLNSYAGRD
>NZ_CP045293.1|WP_152395815.1|5389033_5389528_+|DUF4446-family-protein
MDTMTLEQMQWMIMGVMVLLMVVLLIMFIAQAVKLKKLRRKYDLMMEGTGVNDLENIIIEMKEHIYALREEQSEHTKQVSGIHQQMKKMKSNVGFLRYNPFQGNGSDLSFSLAIVNDEQDGIVLSALHSRENTYVYAKPVEQGESKYPLSPEEMEALNLAQRKN
>NZ_CP045293.1|WP_152395824.1|5398001_5398196_-|YjzC-family-protein
MGERTEFEPGDKAPNNGWYMEVGEASFHTEIQDPKMIELKRGDTFPETTNKDRKWKKKHHAMVH
>NZ_CP045293.1|WP_152395825.1|5398412_5398700_+|30S-ribosomal-protein-S6
MRKYEVMYIIRTDIEQEVVQAAVEKFQGIISNGGGEITKHDVLGKRRLAYEIKKFRDGHYVLVNFTAEPAVVAELERVMKISDEVIRYLITQDVA
>NZ_CP045293.1|WP_152395826.1|5398743_5399238_+|single-stranded-DNA-binding-protein
MLNRVILIGRLTRDPELRYTPAGVAVTQFTIAVDRPFSNQGGEREADFIPVVTWRQLAETCANYLRKGRLTAVEGRIQVRNYDNNEGKRVYVTEVIADNVRFLESGNREGGGSREEAQGSGGFGGGGFGGGSNQGSNRNTSRSNQDPFSDDGKPIDISDDDLPF
>NZ_CP045293.1|WP_078498027.1|5399258_5399540_+|30S-ribosomal-protein-S18
MSFKQRDNNEERGEKKFGGRRGGRNKRRKVCYFTVNKITHIDYKDTDLLRKFISERGKILPRRVTGTSAKYQRLLTIAVKRSRQIALLPYTTE
>NZ_CP045293.1|WP_152395827.1|5399615_5399879_+|DUF1450-domain-containing-protein
MGLGLIVVEVCESNAMAALPLEDLEEEFPEVAIMRTDCLNMCALCKAKSYVMVDNQRVASSDRDICLAKTKEAIKQHLDQFYGAVEE
>NZ_CP045293.1|WP_152395828.1|5400062_5400869_+|TIM-barrel-protein
MKISVEGFSFFHLLQQEMIDVFGYLESLKYRYRVDAAGLWNGYFVNRSEEICQLREVDYIRKIKLALAERSMTVPNIAIDGAHVWDPNPEKRELLYQNALAHLDVAEYLGAQTVRIDTGGFGSTDMTEEQFEYTAKRFQEFAQRAYDGGYRIGPENHSGPSRMPKWMVKLAQAVNHPGYGVLLHMGRWDSDVEAGDSLLAPWVYHVHLDPKYVHPHQIENRMQLLFNHGYDGYWGIEYYAQAAPYAEIESYVSAVKAAYLKQIGVIIR
>NZ_CP045293.1|WP_152397413.1|5401094_5402066_+|LytR-family-transcriptional-regulator
MKKRYIAISLVALVLIGGFIFRKQLVLLGFDLFLSGQVEKKLEGSYEPIEGKKPEESKITPAGDPFSMLLLGIDQRGKEVGRSDTIIYTVARPKDDKILMVSIPRDTYAEIVGKDKEDKINHAFAFGGKKMIIDSVAKLVDEPVDHYATINFQGFIDVVDAMGGVELPITKDIVNKAAEHEKFTVKGGKPIYSGQEALYYVRYREDDHINRSERNMVFLNAIMNRMTQLNQITKVPELISIMGDNFTTDIEPKKIIDLAKDVFTADHREIYSYTLKGEGGRKANHIWYYIPDEKDLSYIHDMIDNWMDPNTKTDQLMVPVKEK
>NZ_CP045293.1|WP_152395829.1|5402112_5402529_+|CBS-domain-containing-protein
MNIAFFLLPKNEVVCLTQESTLRQALERMEYHRYTSVPVLTEDGEYVGTCTEGDLLWFMKNSNGKTTFETAHKVVLKDIPLRSANKPVRIDSNMEDLISLAKVQNFVPVVDDMNKFIGIVRRSEIIGYCEKRVFANKV
>NZ_CP045293.1|WP_018754181.1|5402756_5403068_+|hypothetical-protein
MTKMQKEMDLAKRAKVIEWLKTEVLDHVSRLFKSLWEGSTTRVVDSLSSLIVSSYILGRRLGVPYKELDDSILEKLKKHKQEGHQLEDWYQDISALEEHLRKR
>NZ_CP045293.1|WP_152395830.1|5403073_5403988_+|DUF2232-domain-containing-protein
MKMRWSSALWSIAALLLILSLFTPFQIVTISFIAIPIVVLYATTNVRTFILHMLCVYLVAFLAMGTFGSAAILFAVYFTIPAVVMGRLYRRKASAMAVFVGGTVTVLAESIIMLFVMNTILGFDFNLYLGETVRTSLDPLQTANLMPVGWTPKMTDDLVAMMTQMVPFALIFSSVLIAAVTHTISRRILNRQGVEASKFKPLHEWMLPRSLIWYYFIAVLADMFISDTDTSFVTVVLVNLLPLLKIAFMIQTVCFFFFVAHIKQWNRILPILFVIPLFIFPPLRIIGLLDIAFPIRQSLVKPKM

Crispr_ID: NZ_CP045293_8

• CRISPR_ID: NZ_CP045293_8
• CRISPR_location: 5594899-5595126
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 4 spacers

Consensus repeat of NZ_CP045293_8

Consensus_repeat	Method
TAACTGCCTTTTTGCAGTTATTT	CRISPRCasFinder

spacers of NZ_CP045293_8

>8.1|5594922|28|NZ_CP045293|CRISPRCasFinder
CATACTTGTCGCGCTAGTCCGCGCCAAA
>8.2|5594973|28|NZ_CP045293|CRISPRCasFinder
CACGAGTAATACGGCGGTTTGTACCATT
>8.3|5595024|29|NZ_CP045293|CRISPRCasFinder
TCGCACATTATCCATCTGATCGCGCCGAA
>8.4|5595076|28|NZ_CP045293|CRISPRCasFinder
CATGCGGAACGCGGTTATTTGTGCTATT

CRISPR arrays and Neighbor proteins around NZ_CP045293_8

CRISPR arrays

The CRISPR arrays of NZ_CP045293_8

>merge|NZ_CP045293|8|5594899-5595126|CRISPRCasFinder
TTAGCTCCTTTATGCAGTTAATTCATACTTGTCGCGCTAGTCCGCGCCAAATAACTGCTTTTATGCAGTTATTTCACGAGTAATACGGCGGTTTGTACCATTTAGATGCATTTATGCAGTTATTTTCGCACATTATCCATCTGATCGCGCCGAATAACTGCCTTTTTGCAGTTATTTCATGCGGAACGCGGTTATTTGTGCTATTTAACTGCCTTTATGCAGTTATTT

>NZ_CP045293|8|6|5594899-5595126|CRISPRCasFinder
TTAGCTCCTTTATGCAGTTAATT	CATACTTGTCGCGCTAGTCCGCGCCAAA
TAACTGCTTTTATGCAGTTATTT	CACGAGTAATACGGCGGTTTGTACCATT
TAGATGCATTTATGCAGTTATTT	TCGCACATTATCCATCTGATCGCGCCGAA
TAACTGCCTTTTTGCAGTTATTT	CATGCGGAACGCGGTTATTTGTGCTATT
TAACTGCCTTTATGCAGTTATTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045293.1|WP_152395975.1|5586220_5587585_-|TrkH-family-potassium-uptake-protein	unknown	unknown	gnl|CDD|223246
NZ_CP045293.1|WP_152395971.1|5579149_5580520_+|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_CP045293.1|WP_152395976.1|5587793_5588747_-|phospho-N-acetylmuramoyl-pentapeptide--transferase	unknown	unknown	gnl|CDD|234638
NZ_CP045293.1|WP_152395979.1|5591627_5594777_-|response-regulator	unknown	unknown	gnl|CDD|274362
NZ_CP045293.1|WP_152395988.1|5603819_5604491_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379228
NZ_CP045293.1|WP_152395982.1|5597843_5598851_-|EamA-family-transporter	unknown	unknown	gnl|CDD|307170
NZ_CP045293.1|WP_152395985.1|5600570_5602157_+|PTS-sugar-transporter-subunit-IIA	unknown	unknown	gnl|CDD|273923
NZ_CP045293.1|WP_152395987.1|5602739_5603597_-|fructose-bisphosphate-aldolase	unknown	unknown	gnl|CDD|169068
NZ_CP045293.1|WP_152395984.1|5600013_5600313_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152395974.1|5584461_5586117_-|diguanylate-cyclase	unknown	unknown	gnl|CDD|143635
NZ_CP045293.1|WP_152395980.1|5595319_5596735_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl|CDD|224089
NZ_CP045293.1|WP_152395981.1|5596868_5597822_+|proline-dehydrogenase	unknown	unknown	gnl|CDD|223580
NZ_CP045293.1|WP_152395983.1|5599027_5599897_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|176133
NZ_CP045293.1|WP_152395970.1|5577714_5579175_+|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|225519
NZ_CP045293.1|WP_152395986.1|5602282_5602654_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152395977.1|5588810_5589908_-|amidohydrolase-family-protein	unknown	unknown	gnl|CDD|225070
NZ_CP045293.1|WP_152395978.1|5590033_5591503_-|chemotaxis-protein	unknown	unknown	gnl|CDD|214599
NZ_CP045293.1|WP_152395989.1|5604487_5605057_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152395973.1|5582356_5584375_+|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|223910
NZ_CP045293.1|WP_152395972.1|5580777_5582160_+|sugar-porter-family-MFS-transporter	unknown	unknown	gnl|CDD|182225

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045293.1|WP_152395975.1|5586220_5587585_-|TrkH-family-potassium-uptake-protein	gnl|CDD|223246	COG0168, TrkG, Trk-type K+ transport systems, membrane components [Inorganic ion transport and metabolism].	1.10809e-78
NZ_CP045293.1|WP_152395971.1|5579149_5580520_+|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	1.10759e-41
NZ_CP045293.1|WP_152395976.1|5587793_5588747_-|phospho-N-acetylmuramoyl-pentapeptide--transferase	gnl|CDD|234638	PRK00108, mraY, phospho-N-acetylmuramoyl-pentapeptide-transferase; Provisional.	3.48034e-88
NZ_CP045293.1|WP_152395979.1|5591627_5594777_-|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].	5.95122e-54
NZ_CP045293.1|WP_152395988.1|5603819_5604491_-|GNAT-family-N-acetyltransferase	gnl|CDD|379228	pfam13508, Acetyltransf_7, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.01576e-09
NZ_CP045293.1|WP_152395982.1|5597843_5598851_-|EamA-family-transporter	gnl|CDD|307170	pfam00892, EamA, EamA-like transporter family. This family includes many hypothetical membrane proteins of unknown function. Many of the proteins contain two copies of the aligned region. The family used to be known as DUF6. Members of this family usually carry 5+5 transmembrane domains, and this domain attempts to model five of these.	2.55517e-08
NZ_CP045293.1|WP_152395985.1|5600570_5602157_+|PTS-sugar-transporter-subunit-IIA	gnl|CDD|273923	TIGR02002, PTS_system_glucose-specific_IIABC_component, PTS system, glucose-specific IIBC component. This model represents the combined B and C domains of the PTS transport system enzyme II specific for glucose transport. Many of the genes in this family also include an A domain as part of the same polypeptide and thus should be given the name "PTS system, glucose-specific IIABC component" while the B. subtilus enzyme also contains an enzyme III domain which appears to act independently of the enzyme II domains. This family is most closely related to the N-acetylglucosamine-specific PTS enzymes (TIGR01998). [Transport and binding proteins, Carbohydrates, organic alcohols, and acids].	0
NZ_CP045293.1|WP_152395987.1|5602739_5603597_-|fructose-bisphosphate-aldolase	gnl|CDD|169068	PRK07709, PRK07709, fructose-bisphosphate aldolase; Provisional.	1.68838e-174
NZ_CP045293.1|WP_152395974.1|5584461_5586117_-|diguanylate-cyclase	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.	7.17929e-55
NZ_CP045293.1|WP_152395980.1|5595319_5596735_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl|CDD|224089	COG1167, ARO8, Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs [Transcription / Amino acid transport and metabolism].	2.59321e-143
NZ_CP045293.1|WP_152395981.1|5596868_5597822_+|proline-dehydrogenase	gnl|CDD|223580	COG0506, PutA, Proline dehydrogenase [Amino acid transport and metabolism].	2.90582e-31
NZ_CP045293.1|WP_152395983.1|5599027_5599897_+|LysR-family-transcriptional-regulator	gnl|CDD|176133	cd08442, PBP2_YofA_SoxR_like, The C-terminal substrate binding domain of LysR-type transcriptional regulators, YofA and SoxR, contains the type 2 periplasmic binding fold. YofA is a LysR-like transcriptional regulator of cell growth in Bacillus subtillis. YofA controls cell viability and the formation of constrictions during cell division. YofaA positively regulates expression of the cell division gene ftsW, and thus is essential for cell viability during stationary-phase growth of Bacillus substilis. YofA shows significant homology to SoxR from Arthrobacter sp. TE1826. SoxR is a negative regulator for the sarcosine oxidase gene soxA. Sarcosine oxidase catalyzes the oxidative demethylation of sarcosine, which is involved in the metabolism of creatine and choline. The 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.	4.06746e-73
NZ_CP045293.1|WP_152395970.1|5577714_5579175_+|HAMP-domain-containing-protein	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	4.60015e-50
NZ_CP045293.1|WP_152395977.1|5588810_5589908_-|amidohydrolase-family-protein	gnl|CDD|225070	COG2159, COG2159, Predicted metal-dependent hydrolase of the TIM-barrel fold [General function prediction only].	5.80671e-10
NZ_CP045293.1|WP_152395978.1|5590033_5591503_-|chemotaxis-protein	gnl|CDD|214599	smart00283, MA, Methyl-accepting chemotaxis-like domains (chemotaxis sensory transducer). Thought to undergo reversible methylation in response to attractants or repellants during bacterial chemotaxis.	3.33381e-41
NZ_CP045293.1|WP_152395973.1|5582356_5584375_+|HAMP-domain-containing-protein	gnl|CDD|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	1.17262e-62
NZ_CP045293.1|WP_152395972.1|5580777_5582160_+|sugar-porter-family-MFS-transporter	gnl|CDD|182225	PRK10077, xylE, D-xylose transporter XylE; Provisional.	8.37429e-164

Protein sequences

>NZ_CP045293.1|WP_152395979.1|5591627_5594777_-|response-regulator
MSNFSDMMRIYNKPALKYITIILLFLILLTGMRMTWSSFFTPSEAPRAVRGVIDLRGITLDTRSTYPLNGEWEFYPDKLLTHASTKEQQAHTQFLQVPGNWNQAWANTSDSSYGYGTYRLRILVDPLEQPVSLWIKGIEASSAVEINGIASGGIGSVTSDVGSYEPMNVSYRPSYEGNGTTEIELLIRVANFDDPYYGGIEKSIRFGAQAGIDYVRWYSIGFQLVTFIILLVHSVYALILFLFSRRESTLFIVVLLTMLVGTQIVVSHDHLLLLWLPINYTWAIKIRLLSMMWQTFLILLVFRRFTTANPKSRSVQIYTVALIAYSVVTIAAAAPLVQSTVHFGIFWVLYLFPLAWLVYVIGKMTTDKLDDVDNIFLILSATAILSNILWGLWNAYREFNIVYYPIDMIAILIGFSTYWFKKFFRNVRANTLLNEQLTQADKLKDQFLANTSHELRTPLHGIMNIAQNIVTKEQAQMSDSTRRDMELLITVSRRMSHLLGDLLDVARLKEHRIVLSQEPIKIQAVAPGVIAMLQFLTEGKPVHFRMDIADSLPPVLADEKRLVQILYNLMHNAIKYTNEGTIVISAEIRGEHALVHITDTGVGMDKATLERVFLPYEQGSYGIQDGRGLGLGLSICKQLVELHGGALTVQSEEGKGSTFSFNLPLAEATLMSSTMSEPGPAPLQGMMFRVNDASPASTMAAAAALEWSAPTIPTPLSQSTERAHILAVDDDPVNLNVLVGILAAEPYYITTVSSAREALYQLRAKPWDLLITDVMMPQMSGYELTQHVREHYSVSELPVLLLTARSQPADIYTGFLSGANDYVTKPVDALELKYRIRALITLKQSINERLRMEAAYLQAQIHPHFLFNTLNSIMALSDIDTEKMRQLGEAFASYLRISFDFLNAGKLVELSHELDLVEAYLYIEKERFEDRLSILWEVDPDVHVLFPPLTVQPLVENAVKHGLLSRQKGGTVLIRITAQEGHTRIEVIDNGKGMEQDQVDQLLYQPSKRKGGIGLYNTNRRLIQLYGQGLSIQSRPEVGTTVSFIIPNH
>NZ_CP045293.1|WP_152395978.1|5590033_5591503_-|chemotaxis-protein
MTRSDTLHRRNKLLVNIIWVMLVLGVVVDMLTGAPTSSIIVLVIVGSITCGMATVMTYKRWLSDYVMYFIPIIVTVLTLLLILTGPIITTYFLVFVNLGIMTLYNNFRAQAFSTFLGLALTIYLIISPYKEEMFGNNDPLTIMLYFVLISAPLLASTRFSGQLQQEAAEQREQAITEKDRTQTMIDQISSSLHVLNDFNTKLRQNVTSTSTISQEVTSSFSEVTSSIETQTHSITDMSESVRRIEHTVASLAERSSTMKTLSENSVDLAQQGWIGAEQLSQKIDHVYETIELSAALMKELNAQNERISDIVTSINQISSQTNLLALNAAIEAARAGEHGKGFAVVSSEIQKLAESSRQSTEQIGTILENIRVKTDQAAEQIILGQQSVIDSRDVTKHVAGLISSLSNDSMKVEDQSTQVQQYANDVYRQYMKLTEDIVTIAGTTEVNMASIEEMSASMTTQDERISEIKDSFLQLDKLATDLNNMTQRG
>NZ_CP045293.1|WP_152395977.1|5588810_5589908_-|amidohydrolase-family-protein
MSRPKWHVVFSAIPIGILLITGCTSNTSAAVEPLSEYSPKSELALIQNVRKSKDASQSLHEIYRDLTLIDIHNHDAGHPDPVSKWGQYGIDRIVLFGDISEPSAQTTDQLAWDHYRKAPDHIYPSFAGFPIYEEEGLSIVRDKLEQGYLNIGEIAAASTYSPIVSKVAWKSEHPNDGYFPQIYELAAQYRVPILLHIDPPNGTPIFHLETALEQHPNTTIIFGHGNAYNDPSSLQTLLAKHPNLYIDFFAGFTAYSPDSTNKLQDFIPLIESYPDRFMLSTDSGFGLTAEQAASALYETIDLLTPETAQRVAYQNYERLIELQPPTESQIKKIKELSAELGTKETYRLNKRMANELIFEWSKDKQ
>NZ_CP045293.1|WP_152395976.1|5587793_5588747_-|phospho-N-acetylmuramoyl-pentapeptide--transferase
MTSSLLFALGISFLLVAALTPILIWGLRSLKLTQPIRAELPPEHHAKRGTPLMAGIILLIGVMTSTYLHPQPLVLFIGATFVLFSFVGFMDDFKKAAFQDPSGISGRTKLIFQFTFTITLLLILLFQFDLSSEITLFNNFSLHLPILAYLIIMTLFIVGSANAINFTDGLDGLLINVAIPTFFFFFVISERIEVKTFSLVMVGCLLGLFIYNIYPAKAFMGDTGSLAIGGSLAFLAVIEKVEILIPILFSVYLVEQFSVMLQVWYYKKTKLRIFRMAPIHYHFSLKYGWSENKIVMVFGFISWFSAFISWAIWKFIL
>NZ_CP045293.1|WP_152395975.1|5586220_5587585_-|TrkH-family-potassium-uptake-protein
MFKKLRNWLERRSPAQVISGYYLLAVTVSVLLFNIPAVHRPGVDMSFFDTVFTAVSVVSDTGLGVINVSETFSVFGYFVIMLVLQFGGIGIMAMSTFFWILLGRKIGLRERRLIMVDNNQFALSGLVQLVKEILQIFILTELIGALLFGFHFLRYFPTWQEAFLQGLFASVSAATNAGMDITGNSLIPFAHDYYVQLLTIVLIVFGSIGFPVLIELKAYLSRRKSKLEQPFRFSLFTKLSTLTYGVLLLIGTVLIFALEYQHFFKGMALHESFFYSLFQSATTRSAGLTTMDISEFSHPTLLVMGVLMFIGGSPNSVGGGIRTTTFALNILFIYHFARGNREIKVFRRELHQDDVMKSLAITLLASIMCCLSVIAISISDKQHQLIEIFLEVCSAFGTVGLSTGITPELSTFAKSILIILMFIGRIGLTSFLYIIGGSKKDAKFHYPVERVITG
>NZ_CP045293.1|WP_152395974.1|5584461_5586117_-|diguanylate-cyclase
MWIDFVLFILLFTLFAYIFATVTITNLHKAYLVFHFSMMVWPFCQFAIKATDNPQLQLLYVKIAFVDMSMLTVGWLLFTLFLTGRSPFPRRKVLFTMSVPTICAAIIVILNPYGMFVEPLDGGYIQRTYGPLFWLCITIFIGYVFVSLYMMYLALAGNSSPRIKKQVKQVLTGIVVMTIFILADIALNVVFWQSLKVLPGLTSLGIMLSAIIFVVAIHRDKVFDIVTIAHQDIINTIAHGIVVLDDNETIVEINHSLRPYFELHVGDRFDITSILPHHESTDKTNAFIQTYQQSPLKRAEIEVMFNRDNRRYIHIHAAPIIVRDAMVGRIITFQDMSVLRRLINETNLQNQILHDRNQSLIAIQRELFESNQKLEKMAITDSLTNCYNRHYLTQQLELEVIKNMNHRIPFSLLLVDIDYFKFINDNYGHLAGDRVLCSTVEVIRQNLRQRDILARYGGEEFIIYLPNTTRAQANILAERIKSTVEANKMNISPVTPALSITISVGLLALDNMTLEPVKDSKSTLNELFQSVDEALYQAKREGRNRIVSIAK
>NZ_CP045293.1|WP_152395973.1|5582356_5584375_+|HAMP-domain-containing-protein
MRFSSLFKNYTTSKGGNMMKWRFTIRARLILSFIVILIAPSLAIGLFSYDSASSTVEKQIRQGTEQSVKLLNEKLSSVILENKQNVAFLANTIRNHEDKAQSYTSARQLIEQFQLQHKGIESAYVGTFDGIMIQFPDVKMPDGYDPRNRDWYKASVDKKGNTIVSPPYKSSSTGNMVITISRALEDGSGVIGVDVNLEQILTIAQNMKVGEKGYSIILDQNRRAIVHPTKKAGQVLKENWLDEVYSESSGHVDYELDGSPKIMDFVTNEETGWKIGGTIDVQEFKDAAGPIFRTTVIVIVIGLLAGFVIVYVTVRSILKPLRRLIQAANMVSDGDLTKRVHRESQDEIGILSETFDKMTDSLRTVLQEVADTSMQLSASSQELAAASEESAQASHYTAESMMQLAEGSDEQMNSMNRVDLTVQEMIMGVRQIAESSQTVSQAAVHSSDMVDEGRHSIQKTVHQMESISSSVSQLGESMKGLSDQARSIDDIVQAIAGIASQTNLLALNASIEAARAGEHGRGFAVVAAEVRKLAEQSNSMAQQIAETIQHIQSEMLRSAQDTEKSAAEVTLGIEVMHEAGEAFQRIEQSVNVVATQIQGVSASVQQMAAGTEQMASDILDAKSTTTAMAGNTQSVSATTEEQLASMQEISMSAEELSKMADRLKVVISQFKL
>NZ_CP045293.1|WP_152395972.1|5580777_5582160_+|sugar-porter-family-MFS-transporter
MSLKEHHEEQQVSMKFVTLVSMVAALGGLLFGFDTAVVSGAIGFMKDHFSLNEVEVGWAVSSLIIGCIAGAASAGVLGDRFGRKKVLITAAILFIIGSIGSAIPSTFSGYIIARIIGGIGIGITSTLCPLYNAEIAPAKYRGRLVALNQFATVTGIFLTYFVNLGIAGYGDDAWDIAMGWRWMFGFGVLPGVLFLVLLFFVPESPRWLIKQGKAAESLPILLKIHGEELAKQEVLDIKKSFAQESGSIRQLFSPALRISLIVGVGLAILQQVTGINAVMYYAPEIFKETGAGTNAALVQTILVGLINFLFTILAIWLIDKVGRKVLLLIGSASMAVSLAVIGTAFYTGHTSGMLVLIFILIYVASFAISLGPVVWVIMSEIFPNRIRGKATAIASMALWAADYIVSQTFPPMLASAGPAITFWIFGVMSVITFLFTWRIVPETKGKSLEEIETLLASSKG
>NZ_CP045293.1|WP_152395971.1|5579149_5580520_+|response-regulator
MYRLLIADDEALEREGIEWIVNRMLPNTFEIMHAENGRMAIQKAYEFRPHIILMDIKMPGIQGLEALKEIKAHHPQVKMILVTAYEYFEYAKEALALGVKEYLVKPAKRDHIAALLQRLIDEIDQEKRKREEEIAVRDKFFQLLPLAETEMALVFMSDQVNETEVGQLADIVGVSIDKGCAIVLALPDLGKLPHKEIGNDKKYLFETVKSAAKGFIKQRTGCVVSSMVYWHMAIFLLEEDSSKDAVLREEALGLGTKLIENLHEQHGIDVTVGIGTVGADISGIRRSYFEGVFASTYEQQWGSLCLFEDLAVPRSEDSSDRHADAKFTEHIAERTYVELAIQRIREEREQRTWSVIDNAVTFIQERFREEISLEDVAEHVHLNPHYFSKVFKQQTGETFIDYVTRLRIDKAKVLIGEGQFSLKEVCYLVGYKDPNYFSRVFKKVAKVSPTEYRNQL
>NZ_CP045293.1|WP_152395970.1|5577714_5579175_+|HAMP-domain-containing-protein
MNIRRMLFIVIPALFIASNAVAFFIFQSGITVQKSYNVMLDRVLLYKQIAGQTENNLRTLNVYLSDRNEMSRSNFTQQRNELKQLREGLSAQETISSTAVLVCSYLHMIDTFMAQEDDVMQAFHHTDSLAYAGFYEKAERTAAFIQEEGHQLIDLELSYYQPFYQQIFTHTKSMNGWAVAVFVLNTLISVACAYWISLGITRPIRQLTRTAQQISRGNLQAPSPKIGAHHEFGVLSEAFERMQESLKSLIAKEKEGLERDKLVKSLELEVLQNQMNPHFLFNSLNVLSKLALLEGAEKTSDLTVTMSNLLRYNLRKLDHPVTLRDEVEHAKEYFTIQQARFRDRIRFITEIDERGLDIWVPTLTLQPLLENVFVHGIEGMEQGAEIKLAVSYIPGEVRVSISDNGIGMSEEVRQSLLQHDARPPTAQAKGQSTGLGTRNVFRRLELFYGREDLVDIVSKPGLGTTVLIRFPAAGKEEEDVSLIDRR
>NZ_CP045293.1|WP_152395980.1|5595319_5596735_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MTWIEIDRSSGISLYRQIYDCYRRKILQGEMRSGEQLPSTRELAANLQVSRNIVIEAYEQLLAEGYIEGRHGSGTYVAEGAYLEGIGGQAAPSPLSDALTGHEQRDIIHFRPGIPALDLFPRKLWGKLTEQIYNQAPHDAFGYGKPEGRHELRTAVTRYLRRTRGILCEPEQLLITTGATQALGLIAKLLLASGSEVIVEDPLTHEIHTIFKMPGAELLPIPVDEQGLLTQLLPHDRKPAFTYVTPSHQFPMGGVLPIQRRVQLIQFARATDSYIVEDDYDSEFRYDSAPISSLQGLDPERVIYIGTFSKIVSPALRIGYLILPPSLIERARDLKWLTDLHTPALEQLTLARFIEEGYLERHIAKMKKVYRKRRDFMVQTLQQRFGDNMRIMGSSTGLHLLAEFPGIEFTQDVLSKIEAYGVRVHPVEIHAIRKGTGHEHRILLGYGNVSEANIAEGIRRLAAALSAIQSL
>NZ_CP045293.1|WP_152395981.1|5596868_5597822_+|proline-dehydrogenase
MELQASAAQALKSIARNEQMKSYIQESKDLYPLLARAARRYVAGETRDEAIAEAMELTARGYVTSLEYIGENTRDQAGCEAAHHEFLQLIHTANQAGIQHTISLDLSHIGMVVDAELAYKHLAALAREAGLHGMKVMISAEESAKTDQILAIYRRACEDYANVGITLQAQLHRTERDVEEVLACRGPIRLVKGAYQESPDLALPRSEALNARYLGLADRLIASGRSVSIATHDEVLHQAIRQRGYLQHSNVEIEMLYGIRPDLLKRLRDEGHRVKVYVLYGREWFLYFCHRLSEYPPNLYQAIVDVVMPRDSKEIGY
>NZ_CP045293.1|WP_152395982.1|5597843_5598851_-|EamA-family-transporter
MLKKQTIIGSILCLIASMSWGAMFPVAHVALQQIDPFYFSFIRYFVVAIILTIMLWMKEGRAAFRMEGKGKALLFFGTMAFTVYNMGVFLGQQLMGDAGTIAASIMEVMMPMISIMVVWLTTRKAPNKFTLVSVVIALAGALLVITNGKLAFFVMAGQHLFPLLLIFTGVVGWVIYSMGGTHFKEWSILRYSTLTCLLGSAVSFVVVSAASISGVLPVPTLHTIFSIKYEMAFMILLPGLAALLCWNQGIKLLSPVNGILFINFVPITTFVIMAFQGYQISMYEFYGTLLIIFALLRNNLQQRKAERSVRIESARTVQATSPTRAKEERIKAASS
>NZ_CP045293.1|WP_152395983.1|5599027_5599897_+|LysR-family-transcriptional-regulator
MELNDLRIFQTVAVHGSISRAALELNYVQSNVTARIKLLEKELRTPLFYRHKRGMILNPEGKRLLMHTREILSGVDAMLRSFEDTSSPSGTLEIGIVETVNALPGILSAYYSKYPQVELSLKAGVTEQLLQHVVDMKLDGAFVSGPIRHPLIEQVEVMQEQLVLVSKSPNFTIEELTQRPLLLYNKGCGYREKLESWMKAEGIIPKHIMEFGTFGTIIGSVAAGIGITIFPESSVTDLAVGGTVYCHRIPEPFREITTIFIRRRDAYVTSTLQCFMDEIVARSTSGHVR
>NZ_CP045293.1|WP_152395984.1|5600013_5600313_+|hypothetical-protein
MEQELTKVTMKDIAGCRSSVPCSSICWIVLMRTQIRTDSSACSILCSATGRAPFAEWLEEGQRDGSIRQDLQVEVCTAMISNVMNATIQRIAIRGDILH
>NZ_CP045293.1|WP_152395985.1|5600570_5602157_+|PTS-sugar-transporter-subunit-IIA
MFKNIFGVLQKVGKALMLPVAILPAAGILLALGNVLHNPSLLEWIPALDNDTVRGVSAVMEQAGGIIFDNLSLLFAVGVAIGLAGGDGVAGLAAIIGYLVMNVTMKLIIGITPEMVATNLSYANVLGISTLQTGVFGGIIVGILAAVLYKRFFTIELPSYLGFFAGKRFVPIITAASSLILGIIMVFVWPPIQGGLNAFSHSMIDKNQTLAAFVFGVIERSLIPFGLHHIFYSPFWFEFGQYVNKAGELVRGDQKIFFAQLADGVNLTAGTFMVGKFPFMMFGLPAAALAMYHEARPEHKKLVAGMMGSAALTSFLTGITEPLEFSFLFVAPLLFAVHALFAGLSFMTMQLLNVKIGMTFSGGVIDFLLFGVLPNRTRWWLVIVVGLILAVIYYFGFRFAIRAFNLRTPGREEVTRDRAAVSAKDADELPRNILTALGGQENITSLDACITRLRVTVKNSAGVNKSQLKELGASGVLEVGNNIQAIFGPKSDILKTKISEIITRDSMELEASKDVVKDKDTEKPSDKE
>NZ_CP045293.1|WP_152395986.1|5602282_5602654_+|hypothetical-protein
MFEQDTNLYAAFMEGAGAVRQRADLVIYAANLPSANLKPTLRLEWSEPFGENLPWFLHELPTVFVSFANPYQLYDLPRVPVYVNAYLASEHTVRAVVTKLVGASSFEGSSPVDPFCGSWDAWF
>NZ_CP045293.1|WP_152395987.1|5602739_5603597_-|fructose-bisphosphate-aldolase
MPLVSMKDMLVKALKEGYAVGQFNINNLEWTQAILAAAEEEKSPVILGVSEGAARHMGGFKVVTAMTAALIEEMKITVPVAIHLDHGSSFDKCKAAIDAGFTSVMIDASHHPFAENVETTKKVVEYAHSKGVSVEAELGTVGGQEDDVVADGVIYADPAECAELVKLTGIDCLAPALGSVHGPYKGEPKLGFKEMEEICKSTQLPLVLHGGTGIPTDQIKKSISLGTAKINVNTENQIAFSKKVREVLAADSEAFDPRKYIVPGRDAIKATVIGKIREFGSSNKA
>NZ_CP045293.1|WP_152395988.1|5603819_5604491_-|GNAT-family-N-acetyltransferase
MSGPYSVSKLTKSDKPLFVTLMRRAFARDPLFLHIFGDSEQDRRARGRVEAFVSFLFDKSLLFHEEEVWGVFENERLLGTYLVEKPPTRRPNVSGVLFLTMRLIPLLFQISTRAVNLLNSYMHVTRSAAPSVTHHYLIMIGVQPEAQGKGIGRVMLQHLLDTVNADKNSCGIALDTENKENVHLYQRFGFTLNKETQFDNLSVYCMFHQKISPENDASTLKSE
>NZ_CP045293.1|WP_152395989.1|5604487_5605057_-|hypothetical-protein
MTQIRIPSFLHDVFGEQQSIGSIVSILLFGGLLTTALYVIFPDLTDDLPLWRSALALLLIFDIFAGCVANFTASTSNFYASRRTNRIVFIAIHFHIVIVALLLNTNIWHAIGVWAYTIAGAFIVNALIGKASQRFVAGILLSMGLGGIPLLPSMQPYMLTISLLFLLKVLYSFAVDHYGIAQHPAGDET

Crispr_ID: NZ_CP045293_9

• CRISPR_ID: NZ_CP045293_9
• CRISPR_location: 5789740-5789814
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: WYL

Consensus repeat of NZ_CP045293_9

Consensus_repeat	Method
AAAAAGGCAGTTAATTGAGCTGAG	CRISPRCasFinder

spacers of NZ_CP045293_9

>9.1|5789764|27|NZ_CP045293|CRISPRCasFinder
GTGGCACGATACGTGTGAAATAACTGC

CRISPR arrays and Neighbor proteins around NZ_CP045293_9

CRISPR arrays

The CRISPR arrays of NZ_CP045293_9

>merge|NZ_CP045293|9|5789740-5789814|CRISPRCasFinder
AAAAAGGCAGTTAATTGAGCTGAGGTGGCACGATACGTGTGAAATAACTGCAAAAAAGCAGTTAATTGAGCTGAG

>NZ_CP045293|9|7|5789740-5789814|CRISPRCasFinder
AAAAAGGCAGTTAATTGAGCTGAG	GTGGCACGATACGTGTGAAATAACTGC
AAAAAAGCAGTTAATTGAGCTGAG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045293.1|WP_152396159.1|5795701_5796883_+|biotin/lipoyl-binding-protein	unknown	unknown	gnl|CDD|273776
NZ_CP045293.1|WP_152396155.1|5792200_5792989_+|glyoxalase/bleomycin-resistance/dioxygenase-family-protein	unknown	unknown	gnl|CDD|319939
NZ_CP045293.1|WP_152396145.1|5781702_5782989_-|ammonium-transporter	unknown	unknown	gnl|CDD|223083
NZ_CP045293.1|WP_152396161.1|5798434_5799790_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_CP045293.1|WP_152397435.1|5786202_5786889_+|response-regulator	unknown	unknown	gnl|CDD|223816
NZ_CP045293.1|WP_152396152.1|5789908_5790409_+|hypothetical-protein	unknown	unknown	gnl|CDD|368313
NZ_CP045293.1|WP_152396144.1|5778326_5781590_-|helicase-SNF	unknown	unknown	gnl|CDD|223627
NZ_CP045293.1|WP_152396157.1|5793874_5794738_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|224096
NZ_CP045293.1|WP_152396151.1|5788729_5789686_+|WYL-domain-containing-protein	WYL	COG2378_WYL_CAS-I:CAS-III	gnl|CDD|225253
NZ_CP045293.1|WP_152396150.1|5786885_5788640_+|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|274368
NZ_CP045293.1|WP_152396147.1|5783592_5784021_+|EamA-family-transporter	unknown	unknown	gnl|CDD|225308
NZ_CP045293.1|WP_152396160.1|5796885_5798274_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_CP045293.1|WP_152396153.1|5790510_5790909_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152396156.1|5793023_5793701_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379326
NZ_CP045293.1|WP_152396148.1|5784114_5785215_+|nitric-oxide-synthase	unknown	unknown	gnl|CDD|376957
NZ_CP045293.1|WP_152396158.1|5794760_5795627_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223472
NZ_CP045293.1|WP_152396154.1|5791181_5791811_+|NAD(P)H-binding-protein	unknown	unknown	gnl|CDD|225462
NZ_CP045293.1|WP_152396143.1|5776478_5778242_+|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|225519
NZ_CP045293.1|WP_152396146.1|5783346_5783478_-|DUF4023-domain-containing-protein	unknown	unknown	gnl|CDD|372519
NZ_CP045293.1|WP_152396149.1|5785219_5786173_+|1,4-dihydroxy-2-naphthoate-polyprenyltransferase	unknown	unknown	gnl|CDD|237373

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP045293.1|WP_152396151.1|5788729_5789686_+|WYL-domain-containing-protein	WYL	COG2378_WYL_CAS-I:CAS-III	3.4e-53	175.9	0.1

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045293.1|WP_152396159.1|5795701_5796883_+|biotin/lipoyl-binding-protein	gnl|CDD|273776	TIGR01730, COG0845:_Membrane-fusion_protein, RND family efflux transporter, MFP subunit. This model represents the MFP (membrane fusion protein) component of the RND family of transporters. RND refers to Resistance, Nodulation, and cell Division. It is, in part, a subfamily of pfam00529 (Pfam release 7.5) but hits substantial numbers of proteins missed by that model. The related HlyD secretion protein, for which pfam00529 is named, is outside the scope of this model. Attributed functions imply outward transport. These functions include nodulation, acriflavin resistance, heavy metal efflux, and multidrug resistance proteins. Most members of this family are found in Gram-negative bacteria. The proposed function of MFP proteins is to bring the inner and outer membranes together and enable transport to the outside of the outer membrane. Note, however, that a few members of this family are found in Gram-positive bacteria, where there is no outer membrane. [Transport and binding proteins, Unknown substrate].	1.40283e-31
NZ_CP045293.1|WP_152396145.1|5781702_5782989_-|ammonium-transporter	gnl|CDD|223083	COG0004, AmtB, Ammonia permease [Inorganic ion transport and metabolism].	2.08508e-128
NZ_CP045293.1|WP_152396161.1|5798434_5799790_+|extracellular-solute-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised 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. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. 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.	4.66606e-37
NZ_CP045293.1|WP_152397435.1|5786202_5786889_+|response-regulator	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	5.6695e-77
NZ_CP045293.1|WP_152396152.1|5789908_5790409_+|hypothetical-protein	gnl|CDD|368313	pfam05163, DinB, DinB family. DNA damage-inducible (din) genes in Bacillus subtilis are coordinately regulated and together compose a global regulatory network that has been termed the SOS-like or SOB regulon. This family includes DinB from B. subtilis.	5.34786e-27
NZ_CP045293.1|WP_152396144.1|5778326_5781590_-|helicase-SNF	gnl|CDD|223627	COG0553, HepA, Superfamily II DNA/RNA helicases, SNF2 family [Transcription / DNA replication, recombination, and repair].	3.31268e-104
NZ_CP045293.1|WP_152396157.1|5793874_5794738_+|ABC-transporter-permease-subunit	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	2.53674e-53
NZ_CP045293.1|WP_152396151.1|5788729_5789686_+|WYL-domain-containing-protein	gnl|CDD|225253	COG2378, COG2378, Predicted transcriptional regulator [Transcription].	3.27619e-49
NZ_CP045293.1|WP_152396150.1|5786885_5788640_+|HAMP-domain-containing-protein	gnl|CDD|274368	TIGR02966, Phosphate_regulon_sensor_protein_PhoR, phosphate regulon sensor kinase PhoR. Members of this protein family are the regulatory histidine kinase PhoR associated with the phosphate ABC transporter in most Proteobacteria. Related proteins from Gram-positive organisms are not included in this model. The phoR gene usually is adjacent to the response regulator phoB gene (TIGR02154). [Signal transduction, Two-component systems].	1.15761e-53
NZ_CP045293.1|WP_152396147.1|5783592_5784021_+|EamA-family-transporter	gnl|CDD|225308	COG2510, COG2510, Predicted membrane protein [Function unknown].	2.06501e-36
NZ_CP045293.1|WP_152396160.1|5796885_5798274_+|extracellular-solute-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised 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. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. 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.	1.82079e-35
NZ_CP045293.1|WP_152396155.1|5792200_5792989_+|glyoxalase/bleomycin-resistance/dioxygenase-family-protein	gnl|CDD|319939	cd08351, ChaP_like, ChaP, an enzyme involved in the biosynthesis of the antitumor agent chartreusin (cha), and similar proteins. ChaP is an enzyme involved in the biosynthesis of the potent antitumor agent chartreusin (cha). Cha is an aromatic polyketide glycoside produced by Streptomyces chartreusis. ChaP may play a role as a meta-cleavage dioxygenase in the oxidative rearrangement of the anthracyclic polyketide. ChaP belongs to a conserved domain superfamily that is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases.	7.23855e-09
NZ_CP045293.1|WP_152396156.1|5793023_5793701_+|GNAT-family-N-acetyltransferase	gnl|CDD|379326	pfam13673, Acetyltransf_10, Acetyltransferase (GNAT) domain. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	0.000556958
NZ_CP045293.1|WP_152396148.1|5784114_5785215_+|nitric-oxide-synthase	gnl|CDD|376957	pfam02898, NO_synthase, Nitric oxide synthase, oxygenase domain.	0
NZ_CP045293.1|WP_152396158.1|5794760_5795627_+|ABC-transporter-permease-subunit	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	3.50974e-66
NZ_CP045293.1|WP_152396154.1|5791181_5791811_+|NAD(P)H-binding-protein	gnl|CDD|225462	COG2910, COG2910, Putative NADH-flavin reductase [General function prediction only].	4.42116e-94
NZ_CP045293.1|WP_152396143.1|5776478_5778242_+|HAMP-domain-containing-protein	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	8.9354e-46
NZ_CP045293.1|WP_152396146.1|5783346_5783478_-|DUF4023-domain-containing-protein	gnl|CDD|372519	pfam13215, DUF4023, Protein of unknown function (DUF4023). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are approximately 40 amino acids in length. There is a conserved KLP sequence motif.	0.000849086
NZ_CP045293.1|WP_152396149.1|5785219_5786173_+|1,4-dihydroxy-2-naphthoate-polyprenyltransferase	gnl|CDD|237373	PRK13387, PRK13387, 1,4-dihydroxy-2-naphthoate octaprenyltransferase; Provisional.	3.36753e-86

Protein sequences

>NZ_CP045293.1|WP_152396151.1|5788729_5789686_+|WYL-domain-containing-protein
MNQAERRLALIGVLQRSGMQRAKDLAATFRTSARTIYRDVDALIHAGVPIYGAPGRGYALANQEALPPVSLTAEEALTLLLGIDWIAGQLGPDYRAAAEQIRGKVEGILPSAVKRKADRQRAGLLRASIHPLHQEETLGVMALLRQAIVRETTVRFRYERRDPYPDGTLETVRSVDPYGLVFAAGAWSVMGYCHLRQGIRQFHIDRVFDLVLEPRIFTRPLDVEFHRPAGKNRSMVVIVRFAGDMGHVIAERLSPDVTRMQRTADGWIVTLHVSRMEDACAWILSWGVDAEVLEPEEVKVRIGETASAMLSRYSSGAH
>NZ_CP045293.1|WP_152396150.1|5786885_5788640_+|HAMP-domain-containing-protein
MKKWGSGRLSTKVYWTTAIGFLAFVTLFMVLQLLFFQPYSLKVRSSELEDDFRSMYEQLRDNPMDERWMEELADFDVAHYSLTGVVHKQGLNVDVYLGTRELRAVPLKKARIGDEMKVQIIMADPWQKVTPARPLTPSTPVHPDEESQNKSAPIRTVAAISWYSLDTLRLNDLLQEKLADMLQSPMSGGITAQLFNQGVGVDSNKERVWAAIAPLEQENGQERYLVTVSTLEPVSDAAALLGGFYRYFYIAAVLLLFGFAFLFSRMISNPLVQLNHAAKRLAKLDFSVRTDMKRQDEIGELAQTFDYLATELRDTMGELQEANDQLQQDIEKEKQLERMRKRFVANVSHELKTPISLIQGYAEALRDNVGQGAKRDKYASVIIHESERMSRLVNDLLDLSQLESGKFRLQWSAVPLREHICFVLGTLEQIVSDRMLRLEWLCAEEEILVRSDAQRLQQILTNVLTNAIRYTEAGDRIYITVRPVSDSMEGHDLKVPSDGGSLGSWVQVSIFNSGPSIGEEHLPHIWDAFYRPDESGSRGDTGNGIGLSIVKHLLEMHGSEYSIGNVDGGVEVRFMLPVIPRSEA
>NZ_CP045293.1|WP_152397435.1|5786202_5786889_+|response-regulator
MGEADKSPVILIVDDEQLIRELVVDYLSDEGYLVLQAKNGRDALNLLREQAVDLVVLDVMMPGMNGFEVCEELRTFSSTLVIMLTAKSEDEDKLSGYECGVDDYVTKPFSPKVLAAKINVLLQRFRASDLARDAGGDLYFVMDEAAMELRIGGEVIALSSKEFELLVYLAKHPNQVLSRDSLLDAIWGFDYYGDARAVDTSIKRLRRKLGVEAERIVTVRGSGYKYQS
>NZ_CP045293.1|WP_152396149.1|5785219_5786173_+|1,4-dihydroxy-2-naphthoate-polyprenyltransferase
MTLGRFLQLVEIKTKVASMIPFLMGTFYALYRFHAFHGFHFILMFISLLSFDMATTAINNYYDYKKAVKTEGYGYETHNAIVKYGMRERTVVIIIAVLLILAIGTGIMLVVETGWLIFFIGGLSFCVGILYSFGPIPISRMPLGELFSGLFMGFVILFLSTYIHVPGGELVKLTFDHGIAHLDIQILEVLLLFGVSIPAVLAIANIMLANNICDMDEDVENRRYTLPVYIGRKNALRLFRWIYYAAYVDVFVLFYLGVHPILLLLLFITLIPVNRHVNQFEKLQTKKDTFVLAVRNFMMMNAARIAVYGVAIVMAEL
>NZ_CP045293.1|WP_152396148.1|5784114_5785215_+|nitric-oxide-synthase
MSGLVNREEAMQFIQTCYYEWGRSEEEAKARWSEIEQEMAQRGMYEHTEEELIYGAKLAWRNSNRCIGRLFWDTLTVLDARHVNTEEGIADALIQHLLFATNDGKIRPTITVFRPAMSSQEEIRILNHQLIRYAGYTTDAGIVGDPHSASFTAYCESLGWRGKGGAFDILPLVVQIGSREPKWFELPSPAVLEVPITHPEWSSFTDLGLRWYAVPAVSDMRLEMGGISYPAAPFNGFYMGTEIGARNFADAERYNMLPKVAKIMGLDTSSEATLWRDKALVELNIAVLHSFRERGVSIVDHHTAAQQFMRFEANEAKAERPVTGNWTWLIPPVSPATTHIFHKPYRNEIVKPNFFYRRKVNEQQGE
>NZ_CP045293.1|WP_152396147.1|5783592_5784021_+|EamA-family-transporter
MSWLVYALGSAAMAALVSIFGKIGLKGVDSNTATTIRAVIMMLFLFGVLVFQGKISQIGDVLANKKAMLFIVLSGIAGALSWMFYFIAIQKGDVAKVAPIDKLSVVLAVAFALLFLGEKLSLWGGIGVGLIAIGVLITAFAP
>NZ_CP045293.1|WP_152396146.1|5783346_5783478_-|DUF4023-domain-containing-protein
MDSTRDFVEKVHDTQEKARKNKQHNGQGSPEKKLPGKQHSTGK
>NZ_CP045293.1|WP_152396145.1|5781702_5782989_-|ammonium-transporter
MELGINAVWTMLGAILVLFMQSGFIMLEAGSTRMKNAGHIAGKTIFTIGIVSMVFWAVGYAFIFGSQGTPFLGWGDYFGFSSMAVPEGSVVAPTVNFMFQLAFATISMSVAFGGFAERAKLSAYLIFAIVFSAIIYPVIAHWIWGGGWLAKHGDQDFAGSTVVHLTGAVAAMAATMLLGPRLGKYNKNGKPNNILGHNQVFTTLGVMLLWVGWFGFNAGSTIAAGDGSFFGFIAINTQLGAAAGAVAALLISWMVTGKADISVMLNGALAGLVAITASCAFVESWAAIVIGLIAGIVVFLSMRLFERLRMDDPIYAMSAHGMAGVWGTLANGFFATPELAAKVGVGKAGLFYGGGFEQLGVQALGVIVCAAFTFAISYAVLYLMKITIGIRVTEEEETIGLDLSEHGAYGYPEQMKALAHNSSQGHSA
>NZ_CP045293.1|WP_152396144.1|5778326_5781590_-|helicase-SNF
MQVPLTLKRIRSLCGEKAYERGEAYRLAGQVQFVNKYPLTPYYAATVQDNSAYQVTVEIEPSGDIDAECSCLAFYSYDHYCKHVAAVLIHIHDILHGLDTPSGTRTPHESKTVSRDEQFMQSMLGLFRDKPVRSSATGTFLDARTLLQVEFHCRLIPYGARKFMFGIEIKVGPQRLYVVQRIRDFLEHIERGAPYTFAKHFTYEPTNYRFSKEDDAVLQELIRVHHQDKLYQERSTATSAQAARPASDSRTLLIPPFAWDKTLSFLQFASSVKLEHEGRIHEGITVSDEPIPLRFSFDEGSGDGCELDIQGFDEVTVLEAYNTLLYDSKLLKLKPAEARRIADIRQLIDTARKDQLHIPRAQMESFMEEVVPGLRKLGTVHIAQSISDRIVNTPLMAKLYLDRVNDKLLAGLEFHYGEMIFNPLEDSGQQHGSDRILIRDGEKEQRILALMDQSAFTKTDAGYYMENEDYEYEFLYRVVPELEKLAHIYATSAVKVRLHLPTVPPRITVNADERTDWLEFQFELDGISDAEIRKVVQALEDKRKYYKMPNGAFLPLEGEAFQEIIYLINEFGIRKSEITGTQLRVPIVRGLHLLDTAQPSPYVKLGKSFRKLIEHMRNPDHLDFPVPDSLAAILRDYQVYGFQWMKTLAHYRFGGILADDMGLGKTIQSITFLVSVLPEIRWEKRQALIICPASLVYNWQNELRRFAPEIRAVIADGSKTERSGIIRADDSEADVIITSYPLLRRDVSLYTKRSYHTLILDEAQAFKNYTTQTAQAVRELDARYRFALTGTPIENSLEELWSIFGVVFPDLLPGLKAFGDLSRDTIAKRIRPFLLRRLKSDVLKELPAKIESTQASELLPEQKKLYASFLAELQQETLKHLAEKDFYKTRIQILAGLTRLRQICCHPALFMEGYEGSSAKFEQLFEMIEECRGTGRRLLIFSQFTEMLGMIGRKLSRQGVPYFYLDGQTPSAERVEICHRFNEGERDLFLASLKAGGTGLNLTGADTVILYDLWWNPAVEQQAADRAHRIGQRRVVQVIRLVAQGTVEDKMYELQQRKMNLIDEVIQPGHEGLSALTEQEIREILMI
>NZ_CP045293.1|WP_152396143.1|5776478_5778242_+|HAMP-domain-containing-protein
MQAQTQTKKRMYIPIGFKLMLTYMLFIVIPVIVIGYVSNSMYQNSIRTQTENNIQGTLLQIRDNIEYKLEDVKRVSSMLYFDYSLATQLRSFREGWESYERTTKLVLPKFDIAVNATGMNIAMSIFLENNSLPEVYHGSYERENPDLLGDRAYNLYHLSRIAEKSWYKEFPEEKYAETMEWRQVERDAEFNRISLLRRMVDSLYPKKLKEIGFMRLSVKIPDIFQSVDFGKIGEGTVLSIRDEHERVMYQSGVLPQQVLQAENPADHYLLLEEPLGSMPWKLVAHIPTTIIQRDAQKIRMLIIGVCLVCLLVFTFIGVFVSKYFSVRIQKFVSVLNAFREGDLHKRMFYRGRDEFSQIATALNEMGENIDGLIKKVYLTQLQKKEAELEMLQSQINPHFLYNTLSSINRLAKFGETEKVQQTVLELAKFYRLTLNEGRTMIPVASELEQANAYLEIQKIKYGDRMEVIFDIDPNIWPYVTMKLILQPFIENVLKHAWCGDRIHLRIVGQMEGADILFRVIDDGIGMKQERIDQLFGPEGYMNAGYGIRNVDQRIKLQYGSQYGVSIYSRVGIGTSIQIRIPAQRSKS
>NZ_CP045293.1|WP_152396152.1|5789908_5790409_+|hypothetical-protein
MYQSLQSFIEEYRLESASTQKVLDALTDASLKQEVAPGYRTLGQLAWHLVHNDEGMLLGAGLKFEAPAANGEPPTSASEIAEAYRKVTAALLQALESQWSDASLLEKNNMYGQVWPNGLTLYIYLKHEIHHRGQLTVLMRQAGLQVPGVYGPSKEEWASMGVEAPV
>NZ_CP045293.1|WP_152396153.1|5790510_5790909_-|hypothetical-protein
MLSPVVSTEDAIPITRWEITDLGPASAAKNEDKILQVTAIIDLGEDTIARAAATVQMQEVMFGGSMGRKFIHSIDRSERLTVTTTQDKKLVTNYVKGTVQSDHRLQISYNGYLEKREHVRQPFWGTGFIQIA
>NZ_CP045293.1|WP_152396154.1|5791181_5791811_+|NAD(P)H-binding-protein
MKIAVVGASGKAGSRIVKEALDRGHEVTAIVRDASKVSGNAAVIEKAVFDLTASDLQAFDVVVNAFGAAPGQEHLHVDAGNVLIAALKGSNTRLIVVGGAGSLYVDEAKTLKVMDTPDFPAIYFPTASNQGKNLDILKETTDLKWTFISPSALFALGQRTGSYVKGKDHLLVNSKGESYVSYEDYAVAVVDEIEQPQHIGERFTVVSES
>NZ_CP045293.1|WP_152396155.1|5792200_5792989_+|glyoxalase/bleomycin-resistance/dioxygenase-family-protein
MITHFAGLRLNTMSIQGVKQFYHHQMGFPIQSSSKYTITFQPTPDLTLAFEEVQEPISPAHFAFEVPYSQFGALVDQLQARGITLLTWPDGEAVKTFETGVNVYFRDGDGNILELIAHHDVQEEAISPSGDWQILYMREIGMPAEDVPALTRWMRETLQMGVRDESDWFNFVIGGTAHAVVVSTQRRWIPIQMIALPPRMTVSFGVSDLNQLAARIEPGRTDEMILLNTEDEFKIRKGLYTFRFVRTTLAPDITDRLNLPHF
>NZ_CP045293.1|WP_152396156.1|5793023_5793701_+|GNAT-family-N-acetyltransferase
MIRGGTICNPLITIRRQDIPRAADVLAQGFAKSDPLYRHILPDEATRLHVLKIFFHRYLEMLYPYSDVLTTSDHYEAVALVFRSEREAETWFSKMKYRKQIVMAILKSTPICRMIGVRGFIRGLSILNRMSSSWLSMLGDQEYMHLDMLVVQEPYRGQGYVSRILKPLLAECDERNMLCTLETQTPSNLPIYEHYRFRTLQVIPLQGSTLEQYCMIYSPPGAASK
>NZ_CP045293.1|WP_152396157.1|5793874_5794738_+|ABC-transporter-permease-subunit
MRYTRRARQEIYVALLFLVPSLAGFAIFYLIPFVESVGTSFQSGSGGFTLDQYDAVLGSSSFRNAAGNTIWFTSISVPLIVILSLLIAMWLNQKVYIRNALRTAYVLPLVVPVASIVLLWQITFDWNGALNSILSYFGVERIDWMKTNWSGTVVILMYIWKNLGYNVILFLAGLQNIPASYYETADLEGAGKARQFFGITVIYLIPTTFLVILMSILNSFKVFRETYLLAGDYPHERIYFLQHYMNNMFVSLDMEKLSAAAVIMAVGILGIVGMLFQIERRFRSFME
>NZ_CP045293.1|WP_152396158.1|5794760_5795627_+|ABC-transporter-permease-subunit
MRKIRLSSTLPMLRTLFLASLALIMVTPIVLTVINSFMTEREITANYASLGQTSMRTWVTLKLIPDWVSFDQYMTLLIRTPEFLRMFWNSVGLVVPIIVGQLICASLAAFAFAKLRFPGRDPLFFIYLITLMLPFQVTLVPNYMMVDRLGLLNHMGSIILPGIFAPFGVFLLRQFMINIPSGYMEAARIDGASALRIFLQIILPMVRPGIAALVVLLFADYWNMVEQPLIFLQEAALQPLSLFLTTIQKGAFGVSFAASTLYMIPMVLLFLYAEPHFVEGIEMSGIKG
>NZ_CP045293.1|WP_152396159.1|5795701_5796883_+|biotin/lipoyl-binding-protein
MGARRNKVILTITVIFLSVMAILAFLSNTISAAMLPKVTTERASVQELEVSLSGRGTLQPKEKADVMSDTGFEITDMRVKEGDHVKRGQVLFTLDATDLKDQIADERTRLQQAGLGTKALQQAFIDAQLTGDPVAIDKAKRDLENDRLNRILSERKIARMEKELVEKSRIKAPFDGVIQKVNAKKGDTAAAGKALASVMNTSAGYQFSFTVSEGEASILAVDEKIAVRVKQPGGKEISIQGKVSDMSDASSSSGDAGNAGSGITLGGSKGDSGGAGQGSQEDSGSKMKITIEVNDPKLHGGESVSVSKSKSLGEKGIVISKDRLKKDADGSYLLIVRTKKSPLGNSYVAEKARVRLGAETKDKVIVAQGLNSDDDIIVETSEPLQDGNEVRVK
>NZ_CP045293.1|WP_152396160.1|5796885_5798274_+|extracellular-solute-binding-protein
MNGNRTFEERGDKAMKFKPWGCVGLAGVILLSGCSGGKEAASPKMSDDGKKIVVVGTKGSTRFLQEAEKKFEAAHPDIDIQLKKYGTPEKKNDGGGMQVAPEMTQEEYDRLIQQINTEVLSGKGPDVIDTTGLSLGVYANKGAIEDLHERMKKDSSFKPSDYYEGIWQASEINGGLYALPTSFFIENMMVDTRKLQQAGVKLDDTKWTWKDFFDIAIKVKASSNDEVYALGSNSPKGDLLFSIVESEYDRYVQHDQKTANFDSDEFRQRMQQVKDLYDQGFITQDIGDKDKLIFSQNTMSNSGLLAVMTYLPGWKSILPPTEAGGAAGPSFKAYGGFAINAKSGVKDEAWAFMKFLLSPEMQQSSEFIGIPMLKELVKAQFEESKKLAANKDAFIQIDDADAFNQHVDGMLSLLDQPGKPFAMDPKIQSMMREEFDTFMVGQKSAEEVSKLIQSRVTTYLNE
>NZ_CP045293.1|WP_152396161.1|5798434_5799790_+|extracellular-solute-binding-protein
MKMKFKSWGFLGLAGMIVLAGCSGGKEAGPKMTDDGKKIVVVGTAGSTRFLEEAEKAFEAKHPDIDIQIKKYGPEEKKNDGGGMQAGQVLTRDEYDQFISRLNTEVLSGKGPDLMDTTGLSLGVYANKGAVIDLHDLMKKDQEFKASDYYEGLWKATEIDGGLYALPTNYFVNTMMVDQKRLDQAGVKLDDTKWTWNDFFDIADKIKKSSSDEVYALGTNGPKGELLYSIVEADYKRYVQHEKKTANFDSDEFRQMMQHVKDLYDKGFITNYDGSLDKLMFTQNTYITPDMLAAFTYTKGWKSILPPTSEGSSSGLSFQPMGSYSINAKSGVKDEAWQFMKFMLSPEMQQSPELGGISMLKEQVNAKFDELKQQVQDGTSQMAVKIDDPQDFARHVDEMKALLNNTGQPSAMDPKIRTIISDEFKTFMDGSKSADEVSKLIQSRVTTYLNE

Crispr_ID: NZ_CP045293_10

• CRISPR_ID: NZ_CP045293_10
• CRISPR_location: 6535595-6536137
• CRISPR_type: Unclear
• Repeat_type: NA
• Spacer_info: 10 spacers
• Cas_protein_info: cas3

Consensus repeat of NZ_CP045293_10

Consensus_repeat	Method
CAAAATAACTGCNCAAAANGCAGTTATTTCGCTC	CRT

spacers of NZ_CP045293_10

>10.1|6535628|18|NZ_CP045293|CRT
AAAGTAGCGCGTACGCTC
>10.2|6535679|18|NZ_CP045293|CRT
AAAGAAGCGCCCGCGTCT
>10.3|6535730|18|NZ_CP045293|CRT
AAAGCGGCGCCCGCGCCC
>10.4|6535781|18|NZ_CP045293|CRT
AAAGAAGCGCCCACGCCT
>10.5|6535832|18|NZ_CP045293|CRT
GCAGCAGCGGCTGCTACC
>10.6|6535883|18|NZ_CP045293|CRT
TCAGTAACGCGTGCGCCC
>10.7|6535934|18|NZ_CP045293|CRT
AAAGAAGCGCCCACGCCT
>10.8|6535985|18|NZ_CP045293|CRT
AAAGAAGCGCGTGCGTCT
>10.9|6536036|18|NZ_CP045293|CRT
AAAGCGGCGCCCGCATCT
>10.10|6536087|18|NZ_CP045293|CRT
AAAGTAGCGCCCACGCCC

CRISPR arrays and Neighbor proteins around NZ_CP045293_10

CRISPR arrays

The CRISPR arrays of NZ_CP045293_10

>merge|NZ_CP045293|10|6535595-6536137|CRT
CAAATAACTGCAAAAAAAGCAGTTATTACGCACAAAGTAGCGCGTACGCTCCAAAATAACTGCCAAAAAGCAGTTATTTTGCTCAAAGAAGCGCCCGCGTCTCAAAATAACTGCCAAAAGGCAGTTATTTTGCTCAAAGCGGCGCCCGCGCCCCAAAATAACTGCCAAAAAGCAGTTATTTCGCTCAAAGAAGCGCCCACGCCTCAAAATAACTGCCAAAAAGCAGTTATTTCGCTCGCAGCAGCGGCTGCTACCCCAAATAACTGCAAAAAGGCAGTTATTTCGCTCTCAGTAACGCGTGCGCCCTAAAATAACTGCCAAAAAGCAGTTATTTCGCTCAAAGAAGCGCCCACGCCTCAAAATAACTGCCCAAAAGCAGTTATTTCGTTCAAAGAAGCGCGTGCGTCTCAAAATAACTGCCAAAAGGCAGTTATTTTGCTCAAAGCGGCGCCCGCATCTCCAAATAACTGCCAAAAGGCAGTTATTTCGCTCAAAGTAGCGCCCACGCCCCAAAATAACTGCCAAAAGGCAGTTATTTCGCTC

>NZ_CP045293|10|4|6535595-6536137|CRT
CAAATAACTGCAAAAAAAGCAGTTATTACGCAC	AAAGTAGCGCGTACGCTC
CAAAATAACTGCCAAAAAGCAGTTATTTTGCTC	AAAGAAGCGCCCGCGTCT
CAAAATAACTGCCAAAAGGCAGTTATTTTGCTC	AAAGCGGCGCCCGCGCCC
CAAAATAACTGCCAAAAAGCAGTTATTTCGCTC	AAAGAAGCGCCCACGCCT
CAAAATAACTGCCAAAAAGCAGTTATTTCGCTC	GCAGCAGCGGCTGCTACC
CCAAATAACTGCAAAAAGGCAGTTATTTCGCTC	TCAGTAACGCGTGCGCCC
TAAAATAACTGCCAAAAAGCAGTTATTTCGCTC	AAAGAAGCGCCCACGCCT
CAAAATAACTGCCCAAAAGCAGTTATTTCGTTC	AAAGAAGCGCGTGCGTCT
CAAAATAACTGCCAAAAGGCAGTTATTTTGCTC	AAAGCGGCGCCCGCATCT
CCAAATAACTGCCAAAAGGCAGTTATTTCGCTC	AAAGTAGCGCCCACGCCC
CAAAATAACTGCCAAAAGGCAGTTATTTCGCTC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045293.1|WP_152396689.1|6532478_6533831_+|aminotransferase-class-III-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl|CDD|181078
NZ_CP045293.1|WP_152396685.1|6527386_6527815_-|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_CP045293.1|WP_152396683.1|6523439_6525629_+|DEAD/DEAH-box-helicase	cas3	cd09639_cas3_CAS-I	gnl|CDD|224122
NZ_CP045293.1|WP_152396688.1|6530993_6532457_+|CoA-acylating-methylmalonate-semialdehyde-dehydrogenase	unknown	unknown	gnl|CDD|143404
NZ_CP045293.1|WP_152396693.1|6536288_6537218_+|hypothetical-protein	unknown	unknown	gnl|CDD|277341
NZ_CP045293.1|WP_152397488.1|6539660_6539939_-|DivIVA-domain-containing-protein	unknown	unknown	gnl|CDD|237616
NZ_CP045293.1|WP_152396698.1|6544865_6546212_+|purine-permease	unknown	unknown	gnl|CDD|274468
NZ_CP045293.1|WP_152396699.1|6546518_6546845_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152396690.1|6533844_6534978_+|alanine-dehydrogenase	unknown	unknown	gnl|CDD|240630
NZ_CP045293.1|WP_152396691.1|6535102_6535540_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045293.1|WP_152396694.1|6538355_6539582_+|RtcB-family-protein	unknown	unknown	gnl|CDD|224604
NZ_CP045293.1|WP_152397487.1|6537559_6538351_+|nucleotidyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|313370
NZ_CP045293.1|WP_152396697.1|6543615_6544596_-|Rieske-2Fe-2S-domain-containing-protein	unknown	unknown	gnl|CDD|226985
NZ_CP045293.1|WP_152397486.1|6528096_6528510_+|8-oxo-dGTP-diphosphatase-MutT	unknown	unknown	gnl|CDD|239517
NZ_CP045293.1|WP_152397489.1|6540146_6540881_-|cyclic-nucleotide-binding-domain-containing-protein	unknown	unknown	gnl|CDD|223736
NZ_CP045293.1|WP_152396684.1|6525703_6527362_-|MFS-transporter	unknown	unknown	gnl|CDD|340868
NZ_CP045293.1|WP_152396695.1|6540981_6542268_+|NCS2-family-permease	unknown	unknown	gnl|CDD|225161
NZ_CP045293.1|WP_152396696.1|6542347_6543553_+|anaerobic-sulfatase-maturase	unknown	unknown	gnl|CDD|188457
NZ_CP045293.1|WP_152396687.1|6528871_6530536_+|PucR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|377939
NZ_CP045293.1|WP_152396686.1|6528512_6528845_+|phosphoribosyl-ATP-pyrophosphohydrolase	unknown	unknown	gnl|CDD|212139

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP045293.1|WP_152396683.1|6523439_6525629_+|DEAD/DEAH-box-helicase	cas3	cd09639_cas3_CAS-I	1.8e-12	41.7	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045293.1|WP_152396689.1|6532478_6533831_+|aminotransferase-class-III-fold-pyridoxal-phosphate-dependent-enzyme	gnl|CDD|181078	PRK07678, PRK07678, aminotransferase; Validated.	0
NZ_CP045293.1|WP_152396685.1|6527386_6527815_-|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	6.57423e-23
NZ_CP045293.1|WP_152396683.1|6523439_6525629_+|DEAD/DEAH-box-helicase	gnl|CDD|224122	COG1201, Lhr, Lhr-like helicases [General function prediction only].	2.71863e-140
NZ_CP045293.1|WP_152396688.1|6530993_6532457_+|CoA-acylating-methylmalonate-semialdehyde-dehydrogenase	gnl|CDD|143404	cd07085, ALDH_F6_MMSDH, Methylmalonate semialdehyde dehydrogenase and ALDH family members 6A1 and 6B2. Methylmalonate semialdehyde dehydrogenase (MMSDH, EC=1.2.1.27) [acylating] from Bacillus subtilis is involved in valine metabolism and catalyses the NAD+- and CoA-dependent oxidation of methylmalonate semialdehyde into propionyl-CoA. Mitochondrial human MMSDH ALDH6A1 and Arabidopsis MMSDH ALDH6B2 are also present in this CD.	0
NZ_CP045293.1|WP_152397487.1|6537559_6538351_+|nucleotidyltransferase-domain-containing-protein	gnl|CDD|313370	pfam10127, Nuc-transf, Predicted nucleotidyltransferase. Members of this family of bacterial proteins catalyze the transfer of nucleotide residues from nucleoside diphosphates or triphosphates into dimer or polymer forms.	1.08449e-112
NZ_CP045293.1|WP_152397488.1|6539660_6539939_-|DivIVA-domain-containing-protein	gnl|CDD|237616	PRK14127, PRK14127, cell division regulator GpsB.	4.62727e-14
NZ_CP045293.1|WP_152396698.1|6544865_6546212_+|purine-permease	gnl|CDD|274468	TIGR03173, pbuX, xanthine permease. All the seed members of this model are observed adjacent to genes for either xanthine phosphoribosyltransferase (for the conversion of xanthine to guanine, GenProp0696) or genes for the conversion of xanthine to urate and its concomitant catabolism (GenProp0640, GenProp0688, GenProp0686 and GenProp0687). A number of sequences scoring higher than trusted to this model are found in different genomic contexts, and the possibility exist that these transport related compounds in addition to or instead of xanthine itself. The outgroup to this family are sequences which are characterized as uracil permeases or are adjacent to established uracil phosphoribosyltransferases.	9.86991e-124
NZ_CP045293.1|WP_152396690.1|6533844_6534978_+|alanine-dehydrogenase	gnl|CDD|240630	cd05305, L-AlaDH, Alanine dehydrogenase NAD-binding and catalytic domains. Alanine dehydrogenase (L-AlaDH) catalyzes the NAD-dependent conversion of pyruvate to L-alanine via reductive amination. Like formate dehydrogenase and related enzymes, L-AlaDH is comprised of 2 domains connected by a long alpha helical stretch, each resembling a Rossmann fold NAD-binding domain. The NAD-binding domain is inserted within the linear sequence of the more divergent catalytic domain. Ligand binding and active site residues are found in the cleft between the subdomains. L-AlaDH is typically hexameric and is critical in carbon and nitrogen metabolism in micro-organisms.	0
NZ_CP045293.1|WP_152396694.1|6538355_6539582_+|RtcB-family-protein	gnl|CDD|224604	COG1690, RtcB, Uncharacterized conserved protein [Function unknown].	3.19465e-116
NZ_CP045293.1|WP_152396693.1|6536288_6537218_+|hypothetical-protein	gnl|CDD|277341	cd07396, MPP_Nbla03831, Homo sapiens Nbla03831 and related proteins, metallophosphatase domain. Nbla03831 (also known as LOC56985) is an uncharacterized Homo sapiens protein with a domain that belongs to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	2.34479e-23
NZ_CP045293.1|WP_152396697.1|6543615_6544596_-|Rieske-2Fe-2S-domain-containing-protein	gnl|CDD|226985	COG4638, HcaE, Phenylpropionate dioxygenase and related ring-hydroxylating dioxygenases, large terminal subunit [Inorganic ion transport and metabolism / General function prediction only].	1.06981e-52
NZ_CP045293.1|WP_152397486.1|6528096_6528510_+|8-oxo-dGTP-diphosphatase-MutT	gnl|CDD|239517	cd03425, MutT_pyrophosphohydrolase, The MutT pyrophosphohydrolase is a prototypical Nudix hydrolase that catalyzes the hydrolysis of nucleoside and deoxynucleoside triphosphates (NTPs and dNTPs) by substitution at a beta-phosphorus to yield a nucleotide monophosphate (NMP) and inorganic pyrophosphate (PPi). This enzyme requires two divalent cations for activity; one coordinates the phosphoryl groups of the NTP/dNTP substrate, and the other coordinates to the enzyme. It also contains the Nudix motif, a highly conserved 23-residue block (GX5EX7REUXEEXGU, where U = I, L or V), that functions as metal binding and catalytic site. MutT pyrophosphohydrolase is important in preventing errors in DNA replication by hydrolyzing mutagenic nucleotides such as 8-oxo-dGTP (a product of oxidative damage), which can mispair with template adenine during DNA replication, to guanine nucleotides.	3.86505e-51
NZ_CP045293.1|WP_152397489.1|6540146_6540881_-|cyclic-nucleotide-binding-domain-containing-protein	gnl|CDD|223736	COG0664, Crp, cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases [Signal transduction mechanisms].	3.02955e-45
NZ_CP045293.1|WP_152396684.1|6525703_6527362_-|MFS-transporter	gnl|CDD|340868	cd06179, MFS_TRI12_like, Fungal trichothecene efflux pump (TRI12) of the Major Facilitator Superfamily of transporters. This family includes Fusarium sporotrichioides trichothecene efflux pump (TRI12), which may play a role in F. sporotrichioides self-protection against trichothecenes. TRI12 belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.51761e-58
NZ_CP045293.1|WP_152396695.1|6540981_6542268_+|NCS2-family-permease	gnl|CDD|225161	COG2252, COG2252, Xanthine/uracil/vitamin C permease [Nucleotide transport and metabolism].	5.15092e-116
NZ_CP045293.1|WP_152396696.1|6542347_6543553_+|anaerobic-sulfatase-maturase	gnl|CDD|188457	TIGR03942, sulfatase_rSAM, anaerobic sulfatase-maturating enzyme. Members of this protein family are radical SAM family enzymes, maturases that prepare the oxygen-sensitive radical required in the active site of anaerobic sulfatases. This maturase role has led to many misleading legacy annotations suggesting that this enzyme maturase is instead a sulfatase regulatory protein. All members of the seed alignment are radical SAM enzymes encoded next to or near an anaerobic sulfatase. Note that a single genome may encode more than one sulfatase/maturase pair. [Protein fate, Protein modification and repair].	2.96931e-133
NZ_CP045293.1|WP_152396687.1|6528871_6530536_+|PucR-family-transcriptional-regulator	gnl|CDD|377939	pfam07905, PucR, Purine catabolism regulatory protein-like family. The bacterial proteins found in this family are similar to the purine catabolism regulatory protein expressed by Bacillus subtilis (PucR). PucR is thought to be a transcriptional activator involved in the induction of the purine degradation pathway, and may contain a LysR-like DNA-binding domain. It is similar to LysR-type regulators in that it represses its own expression. The other members of this family are also annotated as being putative regulatory proteins.	5.00773e-40
NZ_CP045293.1|WP_152396686.1|6528512_6528845_+|phosphoribosyl-ATP-pyrophosphohydrolase	gnl|CDD|212139	cd11532, NTP-PPase_COG4997, Nucleoside Triphosphate Pyrophosphohydrolase (EC 3.6.1.8) MazG-like domain found in a group of uncharacterized proteins from archaea and bacteria. The family includes some uncharacterized hypothetical proteins from archaea and bacteria. Although their biological roles remain unclear, the family members show significant sequence similarity to the dimeric 2-deoxyuridine 5'-triphosphate nucleotidohydrolase (dUTP pyrophosphatase or dUTPase) and NTP-PPase MazG proteins. However, unlike typical tandem-domain MazG proteins, the family contains a single MazG-like domain.	2.04121e-32

Protein sequences

>NZ_CP045293.1|WP_152396691.1|6535102_6535540_+|hypothetical-protein
MKHLKSLLMVCLTIVLILSLSNVALAKSSKSTLKSYKITFVSAKLVENNHVGNEWSTGAEVNGQAISVGKSKTLKLKDSDMIILTATAIEEDKVPDEGTESEEVEVSSLTKQKTTSKINVMVTENRGRYSGNTATWTFMFKIEKL
>NZ_CP045293.1|WP_152396690.1|6533844_6534978_+|alanine-dehydrogenase
MLIGVPKEIKNNENRVGMTPSSVVTYINAGHEVLVETNAGAGIGFTDQDYLAAGARIVSTAKEAWAAEMVVKVKEPIPSEYGYFHEGLILYTYLHLAPEPELTKALVDSKVTAIAYETIQLDNGSLPLLTPMSEVAGRMSIQIGARFLEKANGGKGVLLSGVPGVAPAKVAIVGGGIVGANAAKMAIGLGADVSILDISPDRLRQLDDMFQGRVKTIMSNPFNIAETVRNADLVVGAVLIPGARAPRLVTEKMVQSMSPGSVIVDVAIDQGGSIETIDRITTHDNPTYEKHGVVHYAVANMPGAVARTSTLALTNVTTPYGVQIASKGYKQAALDNKALAKGINVVDGHVTYKAVADAHGYAFTDVYAVLNQTAVHA
>NZ_CP045293.1|WP_152396689.1|6532478_6533831_+|aminotransferase-class-III-fold-pyridoxal-phosphate-dependent-enzyme
MSIKREPVDILAKDRKYLWHAMSPYNENVPPMVVTAGEGSWITDLNGNRYLDAMSGLWCVNVGYGREEMAKAAYDQLVAMPYYPLTQSHIPAIELAAKLNEWLEGEYVIFFSNSGSEANETAFKIVRQYHEQSGYPNRYKFISRYRAYHGNSMGALAATGQAQRKYKYEPLGGGFVHVHPPDSYRRPAGMSVEAFNLQCAREIEDTIVWEGEETIAAVIMEPAITGGGVIVPHPVYMEEVQKICHRHGVLLIIDEVICGFGRSGRKFGHMNYDVKPDIVTMAKGLTSGYLPLSATAVRKEIYEAFKSKADYSHLRHVNTFGGTPAACALALKNLEIMEREHLVERSRVLGEKLEAGMAELRDHPLVGDTRRFGFLMGIEVVQNQDTKEPLPLAAIGKIIAECKAKGLIIGKNGDTVAGYNNVLMFSPPLSCTDEDVDFIVNTFKAVMNNQ
>NZ_CP045293.1|WP_152396688.1|6530993_6532457_+|CoA-acylating-methylmalonate-semialdehyde-dehydrogenase
MSEVKTQVMTIKNYINGEWIESASGRYDQVPNPATGEMIAQVPHSTRAELDQAAEAAANAFATWKNVAVPRRARILFRYQQLLVEHWEELAKIVTMENGKSYTEAYGEVQRGIECVEFAAGAPTLMMGNQLPDIATGVESGMYRYPIGVVGGITPFNFPMMVPCWMFPLAIACGNTFVLKPSERTPILANRLAELFEQAGLPKGVLNIVHGSHDVVNGILENERIKAVSFVGSQPVAEYIYRTAAANGKRVQALAGAKNHSIVMPDADLDNAVTNIISAAFGSAGERCMACAVVVAVGDVADELVDRLLQAANGIKIGNGMQSDVFLGPVIREENKARTINYIEIGQSEGAVLVRDGRLDQAVNGDGYFVGPTIFDEVKPGMRIWKDEIFAPVLSIVRAKNLAEAIEIANQSEFANGACLYTDSAKAIRQFREDIDAGMLGVNLGVPAPMAFFPFSGYKKSFYGDLHANGRDGVEFYTRKKMLTARY
>NZ_CP045293.1|WP_152396687.1|6528871_6530536_+|PucR-family-transcriptional-regulator
MEFILTVHDILLRPLFQNAVVVAGEGGLARRVRWVHILEVSNFDQLINGEELILTTGISFHSDPSYAVSYVEELAKQNASCLCIELGQFFDKLPEAMIEAASRHQLPLVIFPHGVRFVDITQDLHSMIINSHHRILQELESVSREFHRLTLTSQGITNVLKLLHTSTKAQVIYVPTQGQPTFNPALPIQTQKRYLEALSSRIPEIPDHKPHVVPMEWAFDNKTMILQSVGALGKTWAYIVMVLDHPPQEYDYLILDSASLSISQDLLRKRYIEERKLYTENLWVDDLLHVRIKDEEQLKSLMGTDFKKLNEAQYRVCLIEFDQQGDQSFHAVEEGTESVGIHLSMVLRSIFEQHAFMPLITLKNNRLIIVAIDLNPKRPSKIRLQQVFDSLRQIQLDEKIEDMDLLIGVGRSYVKLMNAHHSYQEAIRAISLYPCFKKPVMFFEDLGVFQLLFHIDNREMLESFVHSYLGPLIDHDLTRGSELIRTLKVYLDHDGSKQIAAQKLFIVRQSLYYRLEKIAELLGADFIEPENRIALQVALRGYQMLNPDRLLNQD
>NZ_CP045293.1|WP_152396686.1|6528512_6528845_+|phosphoribosyl-ATP-pyrophosphohydrolase
MPTYTYNKLVRDLIPQIIEAQGKRANTSVLEEFDYMEALRVKYREETQEYFEANNNEEALEELADALEVIRALAVGHGASWDELEQIRAKKTEARGGFQNRVYLIDVVED
>NZ_CP045293.1|WP_152397486.1|6528096_6528510_+|8-oxo-dGTP-diphosphatase-MutT
MEQVMKWIDVGAAIIENEAGEILIARRKPGKSQAGLWEFPGGKIESGESIVACIRRELMEELQIDVDIGSYFGTHEHQYETANIRLIAYKVSYLQGEIRLIDHDAYCWVRREVLHTIAFAPADVQFVQMLQEELEEK
>NZ_CP045293.1|WP_152396685.1|6527386_6527815_-|MarR-family-transcriptional-regulator
MPINTELVEVTTLFKTLIKRVTQNWNKRMVHQLTYPQFKMLFKLEKHGPQKVSQLAEALCITSGAVTGAADRLLSEGYIERTRAADDRRVVYIQITEEGRRITHQVMEDQKETIAMFFGSLPDEDIKHLKRIMTTVLAKIDN
>NZ_CP045293.1|WP_152396684.1|6525703_6527362_-|MFS-transporter
MEHLSLKRKITIMIAIMAAMFFAAINQTIGSTAMPRIIAILDGMNLYTWTINIYLLTSTIATVLVGKLSDIYGRKPFLLAGILFFMVGAFLTGTSSDVYQFITYRGIQGIGAGIIMATSFTAIGDLFPPRERGKWTGLMTAVFGFSSVIGPTLGGYMIDNMDWHWVFWIFLPLGVVAFFMIIFLFPKVDRKKSESIDYLGSIFLTTSLVPLLLAFSWAGSEYKWVSPQILGLLAASIISAIIFIFVEKHAKSPVLPLSLFKNRIVTVSNIIGFLMNFGMMGALIYLSFFVQGVLEISPTYAGYVTMPMSIFMMITAAITGQKISKSGKYKRFAMLGVPIMIAGMAIMVFMTNVTMAVISMIIFGIGLGLGMPVFSLATQNAVSHKEIGVATASSQLFRNLGGTIGIAVMGSVMATSLKSNITDKMQSAAAHGVDMTKMDPNIAKQLAAFANPQTLMNKPLITETMAKLPADIQPLFTKMLDMIRDALSSTLSTVFLTGTLVLFLALALVFFLKEIPLRTSNSVPAAAADGEQAKAEGTDVGTKQVFASDSMN
>NZ_CP045293.1|WP_152396683.1|6523439_6525629_+|DEAD/DEAH-box-helicase
MSDHPFYRLAPFIQEYIYRKRWDTLREAQVEACRVLFDTRNHLLIASGTASGKTEAAFFPALTELHHEPSKSVGILYIGPLKALINDQFERLKELLQEAHIPVWHWHGDVPQSEKTKLVRDPSGVLQITPESLEGLLMNRPNAIPALFYDLRYIVIDEVHAFMGADRGMQVLSEIARIERMAGCRPRRIGLSATLSDYATASEWLRAGSVEGVEVVAPQGGRKLRLSIEHFSFPSARDEEQTEHLAQATRAYYDYIYDHTRLKKALVFTNSRSDAELAALELRRTAGRRQEPDVFHVHHGSISAMLREEAEAALRTGHGPAVAMATVTLELGIDLGELERVVQLESPSSCASFVQRLGRSGRRGDMPSEMMFVIPEEEDEQAQLPARMPWTLMRAIAIIELYVRHKWVEPLSLRKKPVGLLYHQTMSVLKSMGEAAPKDLARMILSLPPFQHISPEEYQQFLQYLLQTDHVQRTEVGGLIIGLTGEKTVNNYRFYAVFKDDEEYVVYNGSEEIGSITTVPPPEYCFSLAGKLWKVIEIDRKHKAVYVKPSLGKVDTLWVGGRGDIHTEVMRKMRDVLADNTIYPYLAPRAVNRLERARRLARESGLLEKTVIPAGGDSMFILPWIGTKSFRTLERLVKYRLADRLSLRSIVPMEPYYMVISGRADAETLLAEIQAECSEAIDPLGLLKPDESPYLGKYDEFVLPELVRQAFAEDGLDIEGLRAALSVQE
>NZ_CP045293.1|WP_152396693.1|6536288_6537218_+|hypothetical-protein
MNEYTTVPPLRFGVIADLHQDIMHDGPERLQAFIDRMKVADVDFIIQLGDFCFPIPENEVILRIWNLFEGPKFHVLGNHDMDRNDKLEIQNYLGMPNHYYSFDAGTYHFVVLDANYYKHEDQYVDYNNGNYYAHGEQLPYIPDEQLQWLIDDLSRTDRHTIIFSHQSLHNPTDGVRNRDDVHAALVAANQAAEFPKVIACFNGHNHIDAAITRDGIHYIEVNSTSNQWLGEGYEYDQYEASIRSRRPAMKYVAMYADPLYMTVTIAPNMIQIEGIQSEFVGPAPRERGHEGIVCGHEITATITSRHLMF
>NZ_CP045293.1|WP_152397487.1|6537559_6538351_+|nucleotidyltransferase-domain-containing-protein
MIDMNTRILQELRNIEQEENVRILYACESGSRAWGFPSQDSDYDVRFIYLRPVDWYLSIFDKRDVIERPINDLLDINGWDLRKALNLFRKSNPPLLEWLQSPIQYMEQYTVTEQIRRISPLSFSPKSCMYHYLNMAKGNYRDYLQGDQVKIKKYFYVLRPILACAWIERYDDMPPIAFDTLVERLLPGDGELYQFIQQLLIRKKAGEELDYEPRIHLLNTFIEEHISHFEQKAAALKAAEGTLDDQLDALFRAALTEVWKERK
>NZ_CP045293.1|WP_152396694.1|6538355_6539582_+|RtcB-family-protein
MAYQTIDGVRVWGNPDDGALAQARTCAEHGRVVQTLLMADHHKGYSQPIGGVVAYDGQISPSGVGYDIACGNKAVRTNLMAADVMPKISKIMDQIARHISFGIGRVNNDKVDHALFDDPDWDVYLNVGRQEHDKLKSLARDQLGTVGSGNHYVDLFEEKATGRLWIGNHFGSRGFGHKTASGFINLAAGREFLANAPGEKMDQPPILLDLDSELGDMYYRAMKLAGRYAYAGRDYVIEQVLSLLGAEADFEVHNHHNYAWQETHQGRNAVVVRKGATPSAPGQLGFIGGSMGDISVIVRGKDTEENRSAFYSTVHGAGRIMSRTQAAGRMNWKTRKRSGGQISPQQMRSAVKSYNVELRGAGTDESPFVYRKLQDVLDAHAETIDVLHILKPIGVCMAGADEFDPYKD
>NZ_CP045293.1|WP_152397488.1|6539660_6539939_-|DivIVA-domain-containing-protein
MKNLEEMGIKLNAEEIHSKEFTRSLRGYNEEEVDAYLDEIIKDYELFSRLIKEMQKHIYDMQNAANVEISNTDDLLQRVRELEMFCWGKIKG
>NZ_CP045293.1|WP_152397489.1|6540146_6540881_-|cyclic-nucleotide-binding-domain-containing-protein
MIEINQVPIFSDLPSDALQQIIPLLRERQYKKNHVFMFENDQSDSIFILRSGKVKVYRGQEGKEVIMGIQFPGDVIGEAEALTGDSHRIATIEALEPVAAWQITKKDFLDLVDRYPSILRRAYDIMFARVRVLNRTIRYLTFCDVRTKIANLIMDLYYNFGEQDGIAYKIDMKINHSLLASMVGITRESISKTLNDLQHEGIIEIRQKYIYVLNLKHLERICQETEEVPELRKWQHGTTSEQPV
>NZ_CP045293.1|WP_152396695.1|6540981_6542268_+|NCS2-family-permease
MNSKLGRIFQIDNQQTSIRTEMLAGLTSFITIAYIIAVNGAILSNAGMPYEAATIATVFSALVGCMLMAFWAKSPLILAPGMGDNAFFVFTLVFSFGLTWQQALAAVLIAGIVFFLVSMTKGAVYLSKKIPTSMIHAMTAGIGLFIGFLGLKNGGVIVASEGTFVQLASLRDPHVLTTLLTLVIVVPLFLRGVRGNFLIGIIAGTIIGILLGIVDFSQMGSFQFSMAGYDQVFFAFDFSQLHSFQFWIAVFSLSMVIIFANMGAQLGMLPDTSKFRRSFQANSLSIIAASMFGCSPTTTAAEGAAGIAAGGRSGLTPFIAGLLFIPALFLIPILKIIPSSAIAPVLIVVGCLMIQGMKHVKLDDFTEAFPAYLMIAIMPLTFSIVNGIAFGFIAYPIVKIVTGRRQEVSGAMYVIAALFLVYFILGVK
>NZ_CP045293.1|WP_152396696.1|6542347_6543553_+|anaerobic-sulfatase-maturase
MDSCRTATMEAPAALMWKTVSEECNLACDYCYYSSCHGRPSADIQRIDDELLRKVIQEMMQGSRGSVSFAWQGGEPLLAGLDFFRRVVQYQQHYAPRNTIISNALQTNGTLVTREWAAFFRQYSFLLGVSVDGPAWIHDRRRKTGSGKGSYDRVMQGIEVLREARVDFNILMVIHEDNVHEAEAITTWIDQHQFDFVQFIPGMDFRSQDAGAEGKFLVTAKQYGQFLCQIFDWWYRDGEPCVSVRVFDNWLQRLVGQEPEMCVHRESCPSILILEQNGAAYPCDFYIHEQYRLGDAGEQSLSALMADSAWDAFRSQKQVLADACRACEYVQYCHGGCPRHRVGNAGQDALCESYRMLYAYGEDRMRRLAKMLIGRHGWKLPARNERCMCGSGRKYKSCCAI
>NZ_CP045293.1|WP_152396697.1|6543615_6544596_-|Rieske-2Fe-2S-domain-containing-protein
MIIEDAVLRREWLVACRTDELQEKPLGVMLMGERVVLFRNEEGIHAFKDLCIHRGAKLSLGCVRDGNLVCPYHAWEYDGSGACVKIPQLPADRAIPGKARTFKYACKEEYGLVWVCLDSEQPAPMFALPEWTDESYRNVMWGSTTVEAKPPRVIENFLDVGHLAVVHEGYLGVSTHTIIGDYHVIYDEHSIRSEEIEVFQPDPDGSGQAKNVYYTYEILRPMTVKFTKRDKETDNKMSIVLTVAPKDAETTIAYGILSFNYPMDLSDQEIAAFQDVIFAQDKPVVENQKPEDLPLDLQAELSLACDRMSIAYRRYLKDSGLVWGTA
>NZ_CP045293.1|WP_152396698.1|6544865_6546212_+|purine-permease
MEQQQPNKPQLIVGVNEKIGPVKALLLGLQHVLAMDLYIAPIIIAGILSLSNSNASFFIQMCFFATGIATLIQTGIGLRLPVVQGPSYVPIAAIGAIGSKLGMGAMAGSLIPGALIVMLLGLPLKWFAKAVRKFIPPLVGGTVILIVGIGLMPVGLGNVYHAKGELGTNILIGAVSAIVLVICILLGRNAKGLGTFFRLISVIVAIVAGIITASLFGAVDFSPVKDAAWFSFPKLFPFGAPVFDISAILTMVFVYFIVLIETTGTWFVISSVTGEELTNERLNRASFGEGLGCFVGSLFGGTPMTGYSSNAGLIAITGVGSRMAIMAGGGILVLLGLMPKLSALITCIPESVINGIFCIVCVAIVINGLKVIQHVVLDDRNMMVIGIPVLLTIAITVLPKGATDGLPDFVNYVLSSGLTVGALAAVLLNLLIPNHKEKPAAASKQEVA
>NZ_CP045293.1|WP_152396699.1|6546518_6546845_+|hypothetical-protein
MAGKVAHVYEITAKKQLIGAKVARMCGITAKKQLIGGKVARVCGITAKRQLIGGKVARMCEITAKKQLIGGKVARMCEITAKKQLIGVKVACMCEITAKKQLIGGESV

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP045293.1	286966-286990	0	1.0
NZ_CP045293_3	3.6|3210067|28|NZ_CP045293|CRT	3210067-3210094	28	NZ_CP045293.1	3210525-3210552	2	0.929

1. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to position: 286966-286990, mismatch: 0, identity: 1.0

cgaatcttcttcatcttcttcatca	CRISPR spacer
cgaatcttcttcatcttcttcatca	Protospacer
*************************

2. spacer 3.6|3210067|28|NZ_CP045293|CRT matches to position: 3210525-3210552, mismatch: 2, identity: 0.929

cgcacgacttgagcgttcggcgagccta	CRISPR spacer
cgcacgacttaagcgttcggcgagctta	Protospacer
**********.**************.**

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP045293_4	4.1|3832716|19|NZ_CP045293|CRT	3832716-3832734	19	NZ_CP011166	Xanthomonas citri pv. aurantifolii strain FDC 1609 plasmid pXfc46, complete sequence	7347-7365	0	1.0
NZ_CP045293_4	4.1|3832716|19|NZ_CP045293|CRT	3832716-3832734	19	NZ_CP011161	Xanthomonas citri pv. aurantifolii strain FDC 1559 plasmid pXfc43, complete sequence	29818-29836	0	1.0
NZ_CP045293_4	4.4|3832869|19|NZ_CP045293|CRT	3832869-3832887	19	NZ_CP011166	Xanthomonas citri pv. aurantifolii strain FDC 1609 plasmid pXfc46, complete sequence	7347-7365	0	1.0
NZ_CP045293_4	4.4|3832869|19|NZ_CP045293|CRT	3832869-3832887	19	NZ_CP011161	Xanthomonas citri pv. aurantifolii strain FDC 1559 plasmid pXfc43, complete sequence	29818-29836	0	1.0
NZ_CP045293_1	1.3|286888|22|NZ_CP045293|CRISPRCasFinder	286888-286909	22	MH460463	Dickeya phage vB_DsoM_AD1, complete genome	247188-247209	1	0.955
NZ_CP045293_1	1.3|286888|22|NZ_CP045293|CRISPRCasFinder	286888-286909	22	KJ192399	Vibrio phage CHOED, complete genome	47326-47347	2	0.909
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	LC553734	Escherichia phage EK010 DNA, complete sequence	71520-71544	3	0.88
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MT774393	CrAssphage cr127_1, complete genome	3319-3343	3	0.88
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP011356	Bacillus thuringiensis strain YC-10 plasmid pYC11, complete sequence	2650-2674	3	0.88
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP015182	Bacillus thuringiensis serovar alesti strain BGSC 4C1 plasmid pBMB8291, complete sequence	3730-3754	3	0.88
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_018881	Bacillus thuringiensis Bt407 plasmid BTB_8p, complete sequence	2420-2444	3	0.88
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP004865	Bacillus thuringiensis serovar kurstaki str. YBT-1520 plasmid pBMB8240, complete sequence	3730-3754	3	0.88
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP010099	Bacillus thuringiensis serovar galleriae strain 4G5 plasmid pBMB8, complete sequence	5232-5256	3	0.88
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_020242	Bacillus thuringiensis serovar kurstaki str. HD73 plasmid pHT8_2, complete sequence	4283-4307	3	0.88
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_MG710483	Bacillus thuringiensis serovar israelensis strain Bti-UFT6.51 plasmid pBtiUFT6.51.2, complete sequence	6631-6655	3	0.88
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MH460463	Dickeya phage vB_DsoM_AD1, complete genome	246912-246936	3	0.88
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MG945403	UNVERIFIED: Microviridae sp. isolate 3951-1801, complete genome	1379-1403	3	0.88
NZ_CP045293_7	7.1|5397450|28|NZ_CP045293|CRISPRCasFinder	5397450-5397477	28	NZ_CP048881	Oceanospirillales bacterium S2-4-1H plasmid pC, complete sequence	65109-65136	3	0.893
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP009070	Borreliella afzelii K78 plasmid cp32-3, complete sequence	26607-26631	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	779742-779766	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP013709	Clostridium botulinum strain F634 plasmid pRSJ2_2, complete sequence	11621-11645	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP032054	Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence	381511-381535	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP031276	Staphylococcus xylosus strain 2 plasmid unnamed1, complete sequence	17693-17717	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP016560	Streptomyces clavuligerus strain F613-1 plasmid pSCL4, complete sequence	38768-38792	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP013844	Clostridium botulinum strain A634 plasmid pRSJ19_2, complete sequence	47767-47791	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP031945	Nostoc sphaeroides strain Kutzing En plasmid p4, complete sequence	8244-8268	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MK310183	UNVERIFIED: Phage NC-B, complete genome	6504-6528	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MT647605	Pelagibacter phage Lederberg EXVC029P, complete genome	17393-17417	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP011009	Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence	68536-68560	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_KP342511	Enterococcus faecium isolate N12-493 plasmid pEfm12493, complete sequence	104931-104955	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP024793	Nostoc flagelliforme CCNUN1 plasmid pNFSY08, complete sequence	638975-638999	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_018516	Bacillus thuringiensis HD-789 plasmid pBTHD789-1, complete sequence	234053-234077	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP053970	Bacillus thuringiensis strain FDAARGOS_796 plasmid unnamed2, complete sequence	196400-196424	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP053979	Bacillus thuringiensis strain FDAARGOS_795 plasmid unnamed3, complete sequence	104612-104636	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP013277	Bacillus thuringiensis serovar israelensis strain AM65-52 plasmid pAM65-52-2-350K, complete sequence	322934-322958	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP039723	Bacillus thuringiensis strain BT-59 plasmid p2, complete sequence	90335-90359	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP009348	Bacillus thuringiensis HD1002 plasmid 2, complete sequence	322936-322960	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP009334	Bacillus thuringiensis strain HD1011 plasmid 2, complete sequence	168250-168274	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP045024	Bacillus thuringiensis strain JW-1 plasmid p2, complete sequence	322546-322570	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MT786458	Staphylococcus phage vB_SauH_SAP1, complete genome	15330-15354	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MG557618	Staphylococcus phage HSA30, complete genome	128962-128986	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KX349303	Cyanophage S-RIM14 isolate Sn_11_0110, complete genome	96362-96386	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MH729379	Aerococcus phage vB_AviM_AVP, complete genome	42703-42727	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KX349304	Cyanophage S-RIM14 isolate Sn_18_0910, complete genome	95890-95914	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MG603697	Vibrio phage Vp_R1, complete genome	68863-68887	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KX349306	Cyanophage S-RIM14 isolate W1_23_0910, complete genome	95894-95918	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KX349298	Cyanophage S-RIM14 isolate LIS_02_1110, complete genome	95891-95915	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KY779849	Staphylococcus phage qdsa002, complete genome	34222-34246	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MF001365	Staphylococcus phage SA3, partial genome	3697-3721	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KX349299	Cyanophage S-RIM14 isolate LIS_22_0610, complete genome	95891-95915	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MH159197	Staphylococcus phage VB_SavM_JYL01, complete genome	3789-3813	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MN304941	Staphylococcus phage vB_SauH_IME522, complete genome	8555-8579	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KX349305	Cyanophage S-RIM14 isolate Sn_23_0910, complete genome	95892-95916	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	JF974292	Cyanophage S-SSM2 genomic sequence	149544-149568	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MK250904	Staphylococcus phage VB-SavM-JYL02, complete genome	2361-2385	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KX349300	Cyanophage S-RIM14 isolate Np_11_1211, complete genome	95892-95916	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MH248138	Erwinia phage vB_EamM_Alexandra, complete genome	251976-252000	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KF669649	Bacillus phage CampHawk, complete genome	108382-108406	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_015281	Synechococcus phage S-ShM2, complete genome	95895-95919	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KX349301	Cyanophage S-RIM14 isolate Np_45_0711, complete genome	95891-95915	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KM216423	Staphylococcus phage P108, complete genome	109716-109740	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MK249872	Vibrio phage LP.1, complete genome	5194-5218	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MK415405	Phage FAKO05_000032F, complete genome	75472-75496	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_011421	Bacillus phage SPO1, complete genome	107497-107521	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_019448	Staphylococcus phage GH15, complete genome	30853-30877	4	0.84
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KX349302	Cyanophage S-RIM14 isolate RW_03_0110, complete genome	95891-95915	4	0.84
NZ_CP045293_1	1.2|286840|25|NZ_CP045293|CRISPRCasFinder	286840-286864	25	MH460460	Dickeya phage vB_DsoM_JA13, complete genome	219048-219072	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP009070	Borreliella afzelii K78 plasmid cp32-3, complete sequence	26598-26622	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP031069	Bacillus sp. JAS24-2 plasmid pl626, complete sequence	379597-379621	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP031069	Bacillus sp. JAS24-2 plasmid pl626, complete sequence	379606-379630	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_011412	Clostridium perfringens plasmid pCP8533etx, complete sequence	43769-43793	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_007773	Clostridium perfringens plasmid pCPF5603, complete sequence	46028-46052	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP014283	Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence	407793-407817	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP014283	Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence	407844-407868	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP014283	Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence	407868-407892	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP014283	Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence	407892-407916	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP014283	Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence	407916-407940	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP014283	Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence	407958-407982	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP014283	Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence	408000-408024	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP014283	Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence	408024-408048	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP014283	Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence	408057-408081	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_011255	Borrelia recurrentis A1 plasmid pl35, complete sequence	1325-1349	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_011255	Borrelia recurrentis A1 plasmid pl35, complete sequence	34044-34068	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP022446	Bacillus cereus C1L plasmid pC1L1, complete sequence	652708-652732	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP032614	Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence	96947-96971	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP032614	Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence	96998-97022	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP032614	Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence	97022-97046	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP032614	Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence	97046-97070	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP032614	Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence	97070-97094	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP032614	Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence	97112-97136	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP032614	Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence	97163-97187	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP032614	Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence	97187-97211	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP032614	Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence	97220-97244	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP053838	Aliiarcobacter faecis strain CCUG 66484 plasmid pAFAEC, complete sequence	15718-15742	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP011154	Bacillus cereus strain CMCC P0011 plasmid pRML05, complete sequence	498446-498470	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP011154	Bacillus cereus strain CMCC P0011 plasmid pRML05, complete sequence	498755-498779	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP011154	Bacillus cereus strain CMCC P0011 plasmid pRML05, complete sequence	498773-498797	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP011152	Bacillus cereus strain CMCC P0021 plasmid pRML04, complete sequence	48120-48144	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP011152	Bacillus cereus strain CMCC P0021 plasmid pRML04, complete sequence	48138-48162	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP011152	Bacillus cereus strain CMCC P0021 plasmid pRML04, complete sequence	48447-48471	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	CP020755	Bacillus thuringiensis strain ATCC 10792 plasmid pLDW-16, complete sequence	583626-583650	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	CP020755	Bacillus thuringiensis strain ATCC 10792 plasmid pLDW-16, complete sequence	583743-583767	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_020385	Bacillus thuringiensis serovar thuringiensis str. IS5056 plasmid pIS56-328, complete sequence	224221-224245	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP021062	Bacillus thuringiensis strain ATCC 10792 plasmid poh1, complete sequence	214734-214758	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP021062	Bacillus thuringiensis strain ATCC 10792 plasmid poh1, complete sequence	214851-214875	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP022536	Spiroplasma corruscae strain EC-1 plasmid unnamed, complete sequence	8743-8767	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_016770	Bacteroides phage B124-14, complete genome	2660-2684	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KT895374	Bacillus phage vB_BpuM-BpSp, complete genome	177306-177330	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	AP013401	Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-U-MedDCM-OCT-S37-C49	4664-4688	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	AP013532	Uncultured Mediterranean phage uvMED DNA, complete genome, group G4, isolate: uvMED-CGR-U-MedDCM-OCT-S28-C22	37376-37400	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	AP013489	Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C30A-MedDCM-OCT-S45-C81	14630-14654	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MT311645	Salmonella phage vB_Sen-E22, complete genome	8949-8973	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KX017521	Salmonella phage 118970_sal2, complete genome	40825-40849	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MH447526	Sulfolobus filamentous virus 1 isolate S48, complete genome	22191-22215	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MK064562	Sulfolobales Beppu filamentous virus 1 clone A, partial genome	23002-23026	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_047835	Escherichia phage OSYSP, complete genome	10981-11005	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MG065642	UNVERIFIED: Campylobacter phage A148, complete genome	3494-3518	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	LT960552	Yersinia phage fHe-Yen9-03 genome assembly, complete genome: monopartite	181038-181062	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	AP013488	Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C30A-MedDCM-OCT-S38-C82	18689-18713	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	LR596615	Yersinia phage fHe-Yen9-04 genome assembly, chromosome: I	181462-181486	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MN694275	Marine virus AFVG_250M227, complete genome	39157-39181	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	AP013764	Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C30A-MedDCM-OCT-S40-C140, *** SEQUENCING IN PROGRESS ***	1290-1314	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	HE608841	Bacteroides phage B124-14 complete genome	2660-2684	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MN698245	Pelagibacter phage HTVC111P, complete genome	17190-17214	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MN698248	Pelagibacter phage HTVC202P, complete genome	17627-17651	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	AP013486	Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C30A-MedDCM-OCT-S29-C73	28018-28042	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MK728824	Salmonella phage Seabear, complete genome	39132-39156	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	AP013487	Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C30A-MedDCM-OCT-S33-C83	616-640	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_042116	Yersinia phage fHe-Yen9-04 genome assembly, complete genome: monopartite	181462-181486	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MK448744	Streptococcus phage Javan377, complete genome	22638-22662	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KT997868	Uncultured Mediterranean phage uvDeep-CGR2-KM24-C165, complete genome	34084-34108	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MN956514	Salmonella phage L6jm, complete genome	37302-37326	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MK448745	Streptococcus phage Javan381, complete genome	22638-22662	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	AP014446	Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C43-MedDCM-OCT-S31-C62, *** SEQUENCING IN PROGRESS ***, 3 ordered pieces	8739-8763	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MT774375	CrAssphage cr50_1, complete genome	18756-18780	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	AP014322	Uncultured Mediterranean phage uvMED isolate uvMED-GF-U-MedDCM-OCT-S33-C37, *** SEQUENCING IN PROGRESS ***	19135-19159	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_048062	Salmonella phage Sw2, complete genome	39412-39436	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KU594606	Cyanophage S-RIM32 isolate RW_108_0702, complete genome	13739-13763	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_027297	Salmonella phage Stitch, complete genome	40118-40142	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MG711466	Faecalibacterium phage FP_Toutatis, complete genome	26004-26028	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	AP013559	Uncultured Mediterranean phage uvMED isolate uvMED-CGR-C43-MedDCM-OCT-S32-C95, *** SEQUENCING IN PROGRESS ***, 2 ordered pieces	21317-21341	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MK448923	Streptococcus phage Javan380, complete genome	22638-22662	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	AP014119	Uncultured Mediterranean phage uvMED isolate uvMED-GF-C36-MedDCM-OCT-S41-C69, *** SEQUENCING IN PROGRESS ***	32831-32855	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MW147367	Synechococcus phage S-H9-2, complete genome	140250-140274	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_015269	Enterobacteria phage SPC35, complete genome	36327-36351	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MN022787	Salmonella virus VSe12, complete genome	37542-37566	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NC_031902	Salmonella phage 100268_sal2, complete genome	41714-41738	5	0.8
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MN850632	Escherichia phage alia, complete genome	39494-39518	5	0.8
NZ_CP045293_3	3.4|3209965|28|NZ_CP045293|CRT	3209965-3209992	28	JN106171	Uncultured bacterium plasmid pAKD26, complete sequence	31706-31733	5	0.821
NZ_CP045293_3	3.6|3210067|28|NZ_CP045293|CRT	3210067-3210094	28	NZ_CP012477	Arthrobacter sp. ERGS1:01 isolate water plasmid unnamed2, complete sequence	273891-273918	5	0.821
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	NZ_CP045822	Bacillus subtilis strain MB8_B7 plasmid pBs001, complete sequence	20050-20074	6	0.76
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	MH542234	Staphylococcus phage Terranova, complete genome	130309-130333	6	0.76
NZ_CP045293_1	1.4|286933|25|NZ_CP045293|CRISPRCasFinder	286933-286957	25	KP027447	Staphylococcus phage phiIPLA-C1C, complete genome	97669-97693	6	0.76
NZ_CP045293_3	3.2|3209863|28|NZ_CP045293|CRT	3209863-3209890	28	NZ_KY000062	Agrobacterium genomosp. 3 strain CFBP4424 plasmid pTi_CFBP4424, complete sequence	106723-106750	6	0.786
NZ_CP045293_3	3.2|3209863|28|NZ_CP045293|CRT	3209863-3209890	28	NZ_CP039918	Agrobacterium tumefaciens strain CFBP6626 plasmid pAtCFBP6626a, complete sequence	266776-266803	6	0.786
NZ_CP045293_3	3.2|3209863|28|NZ_CP045293|CRT	3209863-3209890	28	NZ_CP048633	Rhizobium oryzihabitans strain M15 plasmid p1, complete sequence	8000-8027	6	0.786
NZ_CP045293_3	3.2|3209863|28|NZ_CP045293|CRT	3209863-3209890	28	NZ_CP048637	Rhizobium oryzihabitans strain M15 plasmid p5, complete sequence	86336-86363	6	0.786
NZ_CP045293_3	3.4|3209965|28|NZ_CP045293|CRT	3209965-3209992	28	NZ_CP054033	Rhizobium sp. JKLM13E plasmid pPR13E02, complete sequence	257257-257284	6	0.786
NZ_CP045293_3	3.4|3209965|28|NZ_CP045293|CRT	3209965-3209992	28	NZ_CP050093	Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b5, complete sequence	221955-221982	7	0.75
NZ_CP045293_3	3.4|3209965|28|NZ_CP045293|CRT	3209965-3209992	28	NC_008384	Rhizobium leguminosarum bv. viciae 3841 plasmid pRL11, complete sequence	349939-349966	7	0.75
NZ_CP045293_3	3.4|3209965|28|NZ_CP045293|CRT	3209965-3209992	28	NZ_CP054032	Rhizobium sp. JKLM13E plasmid pPR13E01, complete sequence	522666-522693	7	0.75
NZ_CP045293_3	3.12|3210372|28|NZ_CP045293|CRT	3210372-3210399	28	NZ_CP016452	Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence	1487380-1487407	7	0.75
NZ_CP045293_3	3.14|3210474|28|NZ_CP045293|CRT	3210474-3210501	28	NZ_CP050096	Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b3, complete sequence	213221-213248	7	0.75
NZ_CP045293_3	3.14|3210474|28|NZ_CP045293|CRT	3210474-3210501	28	NZ_CP050102	Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b2, complete sequence	194457-194484	7	0.75
NZ_CP045293_3	3.14|3210474|28|NZ_CP045293|CRT	3210474-3210501	28	NZ_CP050107	Rhizobium leguminosarum bv. trifolii strain 4B plasmid pRL4b1, complete sequence	231684-231711	7	0.75
NZ_CP045293_3	3.14|3210474|28|NZ_CP045293|CRT	3210474-3210501	28	NZ_CP018229	Rhizobium leguminosarum strain Vaf-108 plasmid unnamed1, complete sequence	332596-332623	7	0.75
NZ_CP045293_3	3.14|3210474|28|NZ_CP045293|CRT	3210474-3210501	28	NC_017327	Sinorhizobium meliloti SM11 plasmid pSmeSM11c, complete sequence	258857-258884	7	0.75
NZ_CP045293_3	3.14|3210474|28|NZ_CP045293|CRT	3210474-3210501	28	NZ_CP016290	Rhizobium leguminosarum strain Vaf10 plasmid unnamed3, complete sequence	456993-457020	7	0.75
NZ_CP045293_3	3.14|3210474|28|NZ_CP045293|CRT	3210474-3210501	28	NZ_CP050112	Rhizobium leguminosarum bv. trifolii strain 3B plasmid pRL3b5, complete sequence	231684-231711	7	0.75
NZ_CP045293_3	3.14|3210474|28|NZ_CP045293|CRT	3210474-3210501	28	NZ_CP021217	Sinorhizobium meliloti RU11/001 plasmid pSymA, complete sequence	1022116-1022143	7	0.75
NZ_CP045293_3	3.14|3210474|28|NZ_CP045293|CRT	3210474-3210501	28	NZ_CP050089	Rhizobium leguminosarum bv. trifolii strain 23B plasmid pRL23b2, complete sequence	236923-236950	7	0.75
NZ_CP045293_7	7.3|5397552|29|NZ_CP045293|CRISPRCasFinder	5397552-5397580	29	NZ_AP018173	Calothrix sp. NIES-2098 plasmid plasmid1 DNA, complete genome	110125-110153	8	0.724
NZ_CP045293_7	7.6|5397604|29|NZ_CP045293|PILER-CR	5397604-5397632	29	NC_048807	Erwinia phage pEp_SNUABM_01, complete genome	24818-24846	8	0.724

1. spacer 4.1|3832716|19|NZ_CP045293|CRT matches to NZ_CP011166 (Xanthomonas citri pv. aurantifolii strain FDC 1609 plasmid pXfc46, complete sequence) position: , mismatch: 0, identity: 1.0

gtgcgcggcctgggcgcgg	CRISPR spacer
gtgcgcggcctgggcgcgg	Protospacer
*******************

2. spacer 4.1|3832716|19|NZ_CP045293|CRT matches to NZ_CP011161 (Xanthomonas citri pv. aurantifolii strain FDC 1559 plasmid pXfc43, complete sequence) position: , mismatch: 0, identity: 1.0

gtgcgcggcctgggcgcgg	CRISPR spacer
gtgcgcggcctgggcgcgg	Protospacer
*******************

3. spacer 4.4|3832869|19|NZ_CP045293|CRT matches to NZ_CP011166 (Xanthomonas citri pv. aurantifolii strain FDC 1609 plasmid pXfc46, complete sequence) position: , mismatch: 0, identity: 1.0

gtgcgcggcctgggcgcgg	CRISPR spacer
gtgcgcggcctgggcgcgg	Protospacer
*******************

4. spacer 4.4|3832869|19|NZ_CP045293|CRT matches to NZ_CP011161 (Xanthomonas citri pv. aurantifolii strain FDC 1559 plasmid pXfc43, complete sequence) position: , mismatch: 0, identity: 1.0

gtgcgcggcctgggcgcgg	CRISPR spacer
gtgcgcggcctgggcgcgg	Protospacer
*******************

5. spacer 1.3|286888|22|NZ_CP045293|CRISPRCasFinder matches to MH460463 (Dickeya phage vB_DsoM_AD1, complete genome) position: , mismatch: 1, identity: 0.955

aacttcttctgcttcaacttct	CRISPR spacer
aacttcttcggcttcaacttct	Protospacer
********* ************

6. spacer 1.3|286888|22|NZ_CP045293|CRISPRCasFinder matches to KJ192399 (Vibrio phage CHOED, complete genome) position: , mismatch: 2, identity: 0.909

aacttcttctgcttcaacttct	CRISPR spacer
aacttcttcggcttcaacttcc	Protospacer
********* ***********.

7. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to LC553734 (Escherichia phage EK010 DNA, complete sequence) position: , mismatch: 3, identity: 0.88

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcatcttcttcatcttcttcatca	Protospacer
   **********************

8. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MT774393 (CrAssphage cr127_1, complete genome) position: , mismatch: 3, identity: 0.88

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttaatcttcttcatcttcttcatta	Protospacer
. *********************.*

9. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP011356 (Bacillus thuringiensis strain YC-10 plasmid pYC11, complete sequence) position: , mismatch: 3, identity: 0.88

cgaatcttcttcatcttcttcatca	CRISPR spacer
agattcttcttcatctttttcatca	Protospacer
 ** *************.*******

10. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP015182 (Bacillus thuringiensis serovar alesti strain BGSC 4C1 plasmid pBMB8291, complete sequence) position: , mismatch: 3, identity: 0.88

cgaatcttcttcatcttcttcatca	CRISPR spacer
agattcttcttcatctttttcatca	Protospacer
 ** *************.*******

11. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_018881 (Bacillus thuringiensis Bt407 plasmid BTB_8p, complete sequence) position: , mismatch: 3, identity: 0.88

cgaatcttcttcatcttcttcatca	CRISPR spacer
agattcttcttcatctttttcatca	Protospacer
 ** *************.*******

12. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP004865 (Bacillus thuringiensis serovar kurstaki str. YBT-1520 plasmid pBMB8240, complete sequence) position: , mismatch: 3, identity: 0.88

cgaatcttcttcatcttcttcatca	CRISPR spacer
agattcttcttcatctttttcatca	Protospacer
 ** *************.*******

13. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP010099 (Bacillus thuringiensis serovar galleriae strain 4G5 plasmid pBMB8, complete sequence) position: , mismatch: 3, identity: 0.88

cgaatcttcttcatcttcttcatca	CRISPR spacer
ggattcttcttcatctttttcatca	Protospacer
 ** *************.*******

14. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_020242 (Bacillus thuringiensis serovar kurstaki str. HD73 plasmid pHT8_2, complete sequence) position: , mismatch: 3, identity: 0.88

cgaatcttcttcatcttcttcatca	CRISPR spacer
agattcttcttcatctttttcatca	Protospacer
 ** *************.*******

15. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_MG710483 (Bacillus thuringiensis serovar israelensis strain Bti-UFT6.51 plasmid pBtiUFT6.51.2, complete sequence) position: , mismatch: 3, identity: 0.88

cgaatcttcttcatcttcttcatca	CRISPR spacer
agattcttcttcatctttttcatca	Protospacer
 ** *************.*******

16. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MH460463 (Dickeya phage vB_DsoM_AD1, complete genome) position: , mismatch: 3, identity: 0.88

cgaatcttcttcatcttcttcatca	CRISPR spacer
cagatcttcttcgtcttcttcatca	Protospacer
*..*********.************

17. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MG945403 (UNVERIFIED: Microviridae sp. isolate 3951-1801, complete genome) position: , mismatch: 3, identity: 0.88

cgaatcttcttcatcttcttcatca	CRISPR spacer
agaatcttcttcaatttcttcatca	Protospacer
 ************ .**********

18. spacer 7.1|5397450|28|NZ_CP045293|CRISPRCasFinder matches to NZ_CP048881 (Oceanospirillales bacterium S2-4-1H plasmid pC, complete sequence) position: , mismatch: 3, identity: 0.893

tttggtggaaatgtgatctgaaaatacg	CRISPR spacer
tttggttgaaatgtgatctaaaaataag	Protospacer
****** ************.****** *

19. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP009070 (Borreliella afzelii K78 plasmid cp32-3, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
tctatcttcttcatcttcttcatct	Protospacer
.  ********************* 

20. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcatcttcttcatcg	Protospacer
.  *********************.

21. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP013709 (Clostridium botulinum strain F634 plasmid pRSJ2_2, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
actatcttcttcatcttcttcatct	Protospacer
   ********************* 

22. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP032054 (Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcatcttcttcatcg	Protospacer
.  *********************.

23. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP031276 (Staphylococcus xylosus strain 2 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttgttcttcttcatcttcttcatca	Protospacer
. . *********************

24. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP016560 (Streptomyces clavuligerus strain F613-1 plasmid pSCL4, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcatcttcttcatcg	Protospacer
.  *********************.

25. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP013844 (Clostridium botulinum strain A634 plasmid pRSJ19_2, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
actatcttcttcatcttcttcatct	Protospacer
   ********************* 

26. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP031945 (Nostoc sphaeroides strain Kutzing En plasmid p4, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ataatcttcttcatcttcttcagcc	Protospacer
  ******************** * 

27. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MK310183 (UNVERIFIED: Phage NC-B, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcatcttcttcatcgtcttcatca	Protospacer
   ************ *********

28. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MT647605 (Pelagibacter phage Lederberg EXVC029P, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
aagatcttcttcatcttcttcaaca	Protospacer
 ..******************* **

29. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP011009 (Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
atagtcttcttcttcttcttcatca	Protospacer
  *.******** ************

30. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_KP342511 (Enterococcus faecium isolate N12-493 plasmid pEfm12493, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
tgattcttcttcttcttcttcatcc	Protospacer
.** ******** *********** 

31. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP024793 (Nostoc flagelliforme CCNUN1 plasmid pNFSY08, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
aaaatcttcttcatcttcgttatca	Protospacer
 .**************** *.****

32. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_018516 (Bacillus thuringiensis HD-789 plasmid pBTHD789-1, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
atactcttcttcgtcttcttcatca	Protospacer
  * ********.************

33. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP053970 (Bacillus thuringiensis strain FDAARGOS_796 plasmid unnamed2, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
atactcttcttcgtcttcttcatca	Protospacer
  * ********.************

34. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP053979 (Bacillus thuringiensis strain FDAARGOS_795 plasmid unnamed3, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
atactcttcttcgtcttcttcatca	Protospacer
  * ********.************

35. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP013277 (Bacillus thuringiensis serovar israelensis strain AM65-52 plasmid pAM65-52-2-350K, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
atactcttcttcgtcttcttcatca	Protospacer
  * ********.************

36. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP039723 (Bacillus thuringiensis strain BT-59 plasmid p2, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
atactcttcttcgtcttcttcatca	Protospacer
  * ********.************

37. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP009348 (Bacillus thuringiensis HD1002 plasmid 2, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
atactcttcttcgtcttcttcatca	Protospacer
  * ********.************

38. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP009334 (Bacillus thuringiensis strain HD1011 plasmid 2, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
atactcttcttcgtcttcttcatca	Protospacer
  * ********.************

39. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP045024 (Bacillus thuringiensis strain JW-1 plasmid p2, complete sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
atactcttcttcgtcttcttcatca	Protospacer
  * ********.************

40. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MT786458 (Staphylococcus phage vB_SauH_SAP1, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
acaaacttcttcatcttcatcatca	Protospacer
  ** ************* ******

41. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MG557618 (Staphylococcus phage HSA30, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
acaaacttcttcatcttcatcatca	Protospacer
  ** ************* ******

42. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KX349303 (Cyanophage S-RIM14 isolate Sn_11_0110, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ggtatcttcttcatcttcttcagga	Protospacer
 * *******************  *

43. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MH729379 (Aerococcus phage vB_AviM_AVP, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
agaatcttcttcttcttcttcgtcc	Protospacer
 *********** ********.** 

44. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KX349304 (Cyanophage S-RIM14 isolate Sn_18_0910, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ggtatcttcttcatcttcttcagga	Protospacer
 * *******************  *

45. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MG603697 (Vibrio phage Vp_R1, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
tgaatcttcttcatcttctggatct	Protospacer
.******************  *** 

46. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KX349306 (Cyanophage S-RIM14 isolate W1_23_0910, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ggtatcttcttcatcttcttcagga	Protospacer
 * *******************  *

47. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KX349298 (Cyanophage S-RIM14 isolate LIS_02_1110, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ggtatcttcttcatcttcttcagga	Protospacer
 * *******************  *

48. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KY779849 (Staphylococcus phage qdsa002, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
acaaacttcttcatcttcatcatca	Protospacer
  ** ************* ******

49. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MF001365 (Staphylococcus phage SA3, partial genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
acaaacttcttcatcttcatcatca	Protospacer
  ** ************* ******

50. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KX349299 (Cyanophage S-RIM14 isolate LIS_22_0610, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ggtatcttcttcatcttcttcagga	Protospacer
 * *******************  *

51. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MH159197 (Staphylococcus phage VB_SavM_JYL01, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
acaaacttcttcatcttcatcatca	Protospacer
  ** ************* ******

52. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MN304941 (Staphylococcus phage vB_SauH_IME522, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
acaaacttcttcatcttcatcatca	Protospacer
  ** ************* ******

53. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KX349305 (Cyanophage S-RIM14 isolate Sn_23_0910, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ggtatcttcttcatcttcttcagga	Protospacer
 * *******************  *

54. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to JF974292 (Cyanophage S-SSM2 genomic sequence) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ggtatcttcttcatcttcttcagga	Protospacer
 * *******************  *

55. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MK250904 (Staphylococcus phage VB-SavM-JYL02, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
acaaacttcttcatcttcatcatca	Protospacer
  ** ************* ******

56. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KX349300 (Cyanophage S-RIM14 isolate Np_11_1211, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ggtatcttcttcatcttcttcagga	Protospacer
 * *******************  *

57. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MH248138 (Erwinia phage vB_EamM_Alexandra, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
agaatcgtcttcatcttcttcttct	Protospacer
 ***** ************** ** 

58. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KF669649 (Bacillus phage CampHawk, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
agaatcgtcttcatcttcatcatcc	Protospacer
 ***** *********** ***** 

59. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_015281 (Synechococcus phage S-ShM2, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ggtatcttcttcatcttcttcagga	Protospacer
 * *******************  *

60. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KX349301 (Cyanophage S-RIM14 isolate Np_45_0711, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ggtatcttcttcatcttcttcagga	Protospacer
 * *******************  *

61. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KM216423 (Staphylococcus phage P108, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
acaaacttcttcatcttcatcatca	Protospacer
  ** ************* ******

62. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MK249872 (Vibrio phage LP.1, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
tgaatcttcttcatcgtcttcacct	Protospacer
.************** ******.* 

63. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MK415405 (Phage FAKO05_000032F, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
agaatcatcttcatcttcgtcatct	Protospacer
 ***** *********** ***** 

64. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_011421 (Bacillus phage SPO1, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
agaatcgtcttcatcttcatcatcc	Protospacer
 ***** *********** ***** 

65. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_019448 (Staphylococcus phage GH15, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
acaaacttcttcatcttcatcatca	Protospacer
  ** ************* ******

66. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KX349302 (Cyanophage S-RIM14 isolate RW_03_0110, complete genome) position: , mismatch: 4, identity: 0.84

cgaatcttcttcatcttcttcatca	CRISPR spacer
ggtatcttcttcatcttcttcagga	Protospacer
 * *******************  *

67. spacer 1.2|286840|25|NZ_CP045293|CRISPRCasFinder matches to MH460460 (Dickeya phage vB_DsoM_JA13, complete genome) position: , mismatch: 5, identity: 0.8

ataaccatcttcgtcgtcttcggaa	CRISPR spacer
gtaatcatcttcgtcgtcttcgtcg	Protospacer
.***.*****************  .

68. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP009070 (Borreliella afzelii K78 plasmid cp32-3, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcatcttcttcattt	Protospacer
.  ********************. 

69. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP031069 (Bacillus sp. JAS24-2 plasmid pl626, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcttcttcttcatcttcttcatct	Protospacer
.   ******************** 

70. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP031069 (Bacillus sp. JAS24-2 plasmid pl626, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcatcttcttcttct	Protospacer
.  ****************** ** 

71. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_011412 (Clostridium perfringens plasmid pCP8533etx, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
taaatcttcttcatcttcttcaaat	Protospacer
..********************   

72. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_007773 (Clostridium perfringens plasmid pCPF5603, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
taaatcttcttcatcttcttcaaat	Protospacer
..********************   

73. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP014283 (Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcgtcttcttcgtcttcttcatca	Protospacer
.  .********.************

74. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP014283 (Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcgtcttcttcgtcttcttcatca	Protospacer
   .********.************

75. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP014283 (Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcgtcttcttcgtcttcttcatca	Protospacer
   .********.************

76. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP014283 (Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcgtcttcttcgtcttcttcatca	Protospacer
   .********.************

77. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP014283 (Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcgtcttcttcgtcttcttcatca	Protospacer
.  .********.************

78. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP014283 (Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcgtcttcttcgtcttcttcatca	Protospacer
.  .********.************

79. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP014283 (Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcgtcttcttcgtcttcttcatca	Protospacer
   .********.************

80. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP014283 (Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcgtcttcttcgtcttcttcatca	Protospacer
.  .********.************

81. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP014283 (Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcgtcttcttcgtcttcttcatca	Protospacer
   .********.************

82. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_011255 (Borrelia recurrentis A1 plasmid pl35, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ataatcttcgtcatcttcttcatag	Protospacer
  ******* ************* .

83. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_011255 (Borrelia recurrentis A1 plasmid pl35, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ataatcttcgtcatcttcttcatag	Protospacer
  ******* ************* .

84. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP022446 (Bacillus cereus C1L plasmid pC1L1, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcttcttcttcgtcttcttcatca	Protospacer
    ********.************

85. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP032614 (Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcgtcttcttcgtcttcttcatca	Protospacer
.  .********.************

86. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP032614 (Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcgtcttcttcgtcttcttcatca	Protospacer
   .********.************

87. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP032614 (Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcgtcttcttcgtcttcttcatca	Protospacer
   .********.************

88. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP032614 (Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcgtcttcttcgtcttcttcatca	Protospacer
   .********.************

89. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP032614 (Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcgtcttcttcgtcttcttcatca	Protospacer
.  .********.************

90. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP032614 (Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcgtcttcttcgtcttcttcatca	Protospacer
.  .********.************

91. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP032614 (Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcgtcttcttcgtcttcttcatca	Protospacer
   .********.************

92. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP032614 (Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcgtcttcttcgtcttcttcatca	Protospacer
.  .********.************

93. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP032614 (Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcgtcttcttcgtcttcttcatca	Protospacer
   .********.************

94. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP053838 (Aliiarcobacter faecis strain CCUG 66484 plasmid pAFAEC, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
tttatctttttcatcttcttcatct	Protospacer
.  *****.*************** 

95. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP011154 (Bacillus cereus strain CMCC P0011 plasmid pRML05, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcgtcttcttcatct	Protospacer
.  *********.*********** 

96. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP011154 (Bacillus cereus strain CMCC P0011 plasmid pRML05, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcgtcttcttcatct	Protospacer
.  *********.*********** 

97. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP011154 (Bacillus cereus strain CMCC P0011 plasmid pRML05, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcgtcttcttcatct	Protospacer
.  *********.*********** 

98. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP011152 (Bacillus cereus strain CMCC P0021 plasmid pRML04, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcgtcttcttcatct	Protospacer
.  *********.*********** 

99. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP011152 (Bacillus cereus strain CMCC P0021 plasmid pRML04, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcgtcttcttcatct	Protospacer
.  *********.*********** 

100. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP011152 (Bacillus cereus strain CMCC P0021 plasmid pRML04, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcgtcttcttcatct	Protospacer
.  *********.*********** 

101. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to CP020755 (Bacillus thuringiensis strain ATCC 10792 plasmid pLDW-16, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcgtcttcttcatct	Protospacer
.  *********.*********** 

102. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to CP020755 (Bacillus thuringiensis strain ATCC 10792 plasmid pLDW-16, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcgtcttcttcatct	Protospacer
.  *********.*********** 

103. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_020385 (Bacillus thuringiensis serovar thuringiensis str. IS5056 plasmid pIS56-328, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcgtcttcttcatct	Protospacer
.  *********.*********** 

104. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP021062 (Bacillus thuringiensis strain ATCC 10792 plasmid poh1, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcgtcttcttcatct	Protospacer
.  *********.*********** 

105. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP021062 (Bacillus thuringiensis strain ATCC 10792 plasmid poh1, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcgtcttcttcatct	Protospacer
.  *********.*********** 

106. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP022536 (Spiroplasma corruscae strain EC-1 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcattttcttcatcttcttcatct	Protospacer
   **.****************** 

107. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_016770 (Bacteroides phage B124-14, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
tgaatcttcttcatcttcatcaatg	Protospacer
.***************** *** ..

108. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KT895374 (Bacillus phage vB_BpuM-BpSp, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcttcctcttcttcatct	Protospacer
.  ********* *********** 

109. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to AP013401 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-U-MedDCM-OCT-S37-C49) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aatatcttcttcatcttcttcaacc	Protospacer
 . ******************* * 

110. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to AP013532 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G4, isolate: uvMED-CGR-U-MedDCM-OCT-S28-C22) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
cgtatcttcttcatcttcttctggc	Protospacer
** ******************    

111. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to AP013489 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C30A-MedDCM-OCT-S45-C81) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aatatcttcttcatcttcttcaaaa	Protospacer
 . *******************  *

112. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MT311645 (Salmonella phage vB_Sen-E22, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
gtcatcttcttcatcatcttcatcg	Protospacer
   ************ ********.

113. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KX017521 (Salmonella phage 118970_sal2, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
gtcatcttcttcatcatcttcatcg	Protospacer
   ************ ********.

114. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MH447526 (Sulfolobus filamentous virus 1 isolate S48, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
tctctcttcttcatcttcttcaaca	Protospacer
.   ****************** **

115. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MK064562 (Sulfolobales Beppu filamentous virus 1 clone A, partial genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
tctctcttcttcatcttcttcaaca	Protospacer
.   ****************** **

116. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_047835 (Escherichia phage OSYSP, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
gtcatcttcttcatcatcttcatcg	Protospacer
   ************ ********.

117. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MG065642 (UNVERIFIED: Campylobacter phage A148, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
gtcatcttcttcatcatcttcatcg	Protospacer
   ************ ********.

118. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to LT960552 (Yersinia phage fHe-Yen9-03 genome assembly, complete genome: monopartite) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aaaatcttcttcttcttcttcattc	Protospacer
 .********** **********. 

119. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to AP013488 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C30A-MedDCM-OCT-S38-C82) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aatatcttcttcatcttcttcaaaa	Protospacer
 . *******************  *

120. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to LR596615 (Yersinia phage fHe-Yen9-04 genome assembly, chromosome: I) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aaaatcttcttcttcttcttcattc	Protospacer
 .********** **********. 

121. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MN694275 (Marine virus AFVG_250M227, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aagttctccttcatcttcttcatca	Protospacer
 .. ***.*****************

122. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to AP013764 (Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C30A-MedDCM-OCT-S40-C140, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aatatcttcttcatcttcttcaaaa	Protospacer
 . *******************  *

123. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to HE608841 (Bacteroides phage B124-14 complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
tgaatcttcttcatcttcatcaatg	Protospacer
.***************** *** ..

124. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MN698245 (Pelagibacter phage HTVC111P, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aatatcttcttcatcttcttcaaaa	Protospacer
 . *******************  *

125. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MN698248 (Pelagibacter phage HTVC202P, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aatatcttcttcatcttcttcaaaa	Protospacer
 . *******************  *

126. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to AP013486 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C30A-MedDCM-OCT-S29-C73) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aatatcttcttcatcttcttcaaaa	Protospacer
 . *******************  *

127. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MK728824 (Salmonella phage Seabear, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
gtcatcttcttcatcatcttcatcg	Protospacer
   ************ ********.

128. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to AP013487 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G19, isolate: uvMED-CGR-C30A-MedDCM-OCT-S33-C83) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aatatcttcttcatcttcttcaaaa	Protospacer
 . *******************  *

129. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_042116 (Yersinia phage fHe-Yen9-04 genome assembly, complete genome: monopartite) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aaaatcttcttcttcttcttcattc	Protospacer
 .********** **********. 

130. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MK448744 (Streptococcus phage Javan377, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttctttatcttcttcatct	Protospacer
.  ********.************ 

131. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KT997868 (Uncultured Mediterranean phage uvDeep-CGR2-KM24-C165, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aaaatcttcttcatcttcttcgata	Protospacer
 .*******************. .*

132. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MN956514 (Salmonella phage L6jm, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
gtcatcttcttcatcatcttcatcg	Protospacer
   ************ ********.

133. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MK448745 (Streptococcus phage Javan381, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttctttatcttcttcatct	Protospacer
.  ********.************ 

134. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to AP014446 (Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C43-MedDCM-OCT-S31-C62, *** SEQUENCING IN PROGRESS ***, 3 ordered pieces) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aatatcttcttcatcttcttcaaaa	Protospacer
 . *******************  *

135. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MT774375 (CrAssphage cr50_1, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
tttttcttcttcctcttcttcatca	Protospacer
.   ******** ************

136. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to AP014322 (Uncultured Mediterranean phage uvMED isolate uvMED-GF-U-MedDCM-OCT-S33-C37, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
agaatcttcttcatcttctttagat	Protospacer
 *******************.*   

137. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_048062 (Salmonella phage Sw2, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
gtcatcttcttcatcatcttcatcg	Protospacer
   ************ ********.

138. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KU594606 (Cyanophage S-RIM32 isolate RW_108_0702, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttcctcatcttcttcatct	Protospacer
.  ******.************** 

139. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_027297 (Salmonella phage Stitch, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
gtcatcttcttcatcatcttcatcg	Protospacer
   ************ ********.

140. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MG711466 (Faecalibacterium phage FP_Toutatis, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
tccgtcttgttcatcttcttcatca	Protospacer
.  .**** ****************

141. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to AP013559 (Uncultured Mediterranean phage uvMED isolate uvMED-CGR-C43-MedDCM-OCT-S32-C95, *** SEQUENCING IN PROGRESS ***, 2 ordered pieces) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aatatcttcttcatcttcttcaaaa	Protospacer
 . *******************  *

142. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MK448923 (Streptococcus phage Javan380, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
ttcatcttctttatcttcttcatct	Protospacer
.  ********.************ 

143. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to AP014119 (Uncultured Mediterranean phage uvMED isolate uvMED-GF-C36-MedDCM-OCT-S41-C69, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
aaaatcttcttcatcttcttcgata	Protospacer
 .*******************. .*

144. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MW147367 (Synechococcus phage S-H9-2, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcgtcgtcttcatcttcttcatca	Protospacer
   .** ******************

145. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_015269 (Enterobacteria phage SPC35, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
atcatcttcttcatcatcttcatcg	Protospacer
   ************ ********.

146. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MN022787 (Salmonella virus VSe12, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
gtcatcttcttcatcatcttcatcg	Protospacer
   ************ ********.

147. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NC_031902 (Salmonella phage 100268_sal2, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
gtcatcttcttcatcatcttcatcg	Protospacer
   ************ ********.

148. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MN850632 (Escherichia phage alia, complete genome) position: , mismatch: 5, identity: 0.8

cgaatcttcttcatcttcttcatca	CRISPR spacer
gtaatcttcttcatcttcttcccaa	Protospacer
  ******************* . *

149. spacer 3.4|3209965|28|NZ_CP045293|CRT matches to JN106171 (Uncultured bacterium plasmid pAKD26, complete sequence) position: , mismatch: 5, identity: 0.821

caggcgatctgtgcgagcggcgagccta	CRISPR spacer
gatgcgatctgagcgagcggcgcgcctg	Protospacer
 * ******** ********** ****.

150. spacer 3.6|3210067|28|NZ_CP045293|CRT matches to NZ_CP012477 (Arthrobacter sp. ERGS1:01 isolate water plasmid unnamed2, complete sequence) position: , mismatch: 5, identity: 0.821

cgcacgacttgagcgttcggcgagccta	CRISPR spacer
cgcacgacaggagcgttcggcgaacttg	Protospacer
********  *************.*.*.

151. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to NZ_CP045822 (Bacillus subtilis strain MB8_B7 plasmid pBs001, complete sequence) position: , mismatch: 6, identity: 0.76

cgaatcttcttcatcttcttcatca	CRISPR spacer
taaatcttcttcatcttcttctaag	Protospacer
..*******************   .

152. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to MH542234 (Staphylococcus phage Terranova, complete genome) position: , mismatch: 6, identity: 0.76

cgaatcttcttcatcttcttcatca	CRISPR spacer
aaggctttcttcatcttcttcatca	Protospacer
 .....*******************

153. spacer 1.4|286933|25|NZ_CP045293|CRISPRCasFinder matches to KP027447 (Staphylococcus phage phiIPLA-C1C, complete genome) position: , mismatch: 6, identity: 0.76

cgaatcttcttcatcttcttcatca	CRISPR spacer
aaggctttcttcatcttcttcatca	Protospacer
 .....*******************

154. spacer 3.2|3209863|28|NZ_CP045293|CRT matches to NZ_KY000062 (Agrobacterium genomosp. 3 strain CFBP4424 plasmid pTi_CFBP4424, complete sequence) position: , mismatch: 6, identity: 0.786

tggacgattagagcgagcggcgagccta	CRISPR spacer
tggaccattcgagcgagcggcgaaagaa	Protospacer
***** *** *************.   *

155. spacer 3.2|3209863|28|NZ_CP045293|CRT matches to NZ_CP039918 (Agrobacterium tumefaciens strain CFBP6626 plasmid pAtCFBP6626a, complete sequence) position: , mismatch: 6, identity: 0.786

tggacgattagagcgagcggcgagccta	CRISPR spacer
tggaccattcgagcgagcggcgaaagaa	Protospacer
***** *** *************.   *

156. spacer 3.2|3209863|28|NZ_CP045293|CRT matches to NZ_CP048633 (Rhizobium oryzihabitans strain M15 plasmid p1, complete sequence) position: , mismatch: 6, identity: 0.786

tggacgattagagcgagcggcgagccta	CRISPR spacer
tggaccattcgagcgagcggcgaaagaa	Protospacer
***** *** *************.   *

157. spacer 3.2|3209863|28|NZ_CP045293|CRT matches to NZ_CP048637 (Rhizobium oryzihabitans strain M15 plasmid p5, complete sequence) position: , mismatch: 6, identity: 0.786

tggacgattagagcgagcggcgagccta	CRISPR spacer
tggaccattcgagcgagcggcgaaagaa	Protospacer
***** *** *************.   *

158. spacer 3.4|3209965|28|NZ_CP045293|CRT matches to NZ_CP054033 (Rhizobium sp. JKLM13E plasmid pPR13E02, complete sequence) position: , mismatch: 6, identity: 0.786

caggcgatctgtgcgagcggcgagccta	CRISPR spacer
tcggcgatctgggcgagcggcgaaccac	Protospacer
. ********* ***********.**  

159. spacer 3.4|3209965|28|NZ_CP045293|CRT matches to NZ_CP050093 (Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b5, complete sequence) position: , mismatch: 7, identity: 0.75

caggcgatctgtgcgagcggcgagccta	CRISPR spacer
gaggcgatccgtgcgagcggcgtatcat	Protospacer
 ********.************ ..*  

160. spacer 3.4|3209965|28|NZ_CP045293|CRT matches to NC_008384 (Rhizobium leguminosarum bv. viciae 3841 plasmid pRL11, complete sequence) position: , mismatch: 7, identity: 0.75

caggcgatctgtgcgagcggcgagccta	CRISPR spacer
gaggcgatccgtgcgagcggcgtatcat	Protospacer
 ********.************ ..*  

161. spacer 3.4|3209965|28|NZ_CP045293|CRT matches to NZ_CP054032 (Rhizobium sp. JKLM13E plasmid pPR13E01, complete sequence) position: , mismatch: 7, identity: 0.75

caggcgatctgtgcgagcggcgagccta	CRISPR spacer
aaggcgagctgtccgagcggcgagttcc	Protospacer
 ****** **** ***********... 

162. spacer 3.12|3210372|28|NZ_CP045293|CRT matches to NZ_CP016452 (Sinorhizobium sp. RAC02 plasmid pBSY16_1, complete sequence) position: , mismatch: 7, identity: 0.75

caggcggtttgagcgagcggtgagccta	CRISPR spacer
gcgagggtttgagcgagctgtgagccgg	Protospacer
  *. ************* ******* .

163. spacer 3.14|3210474|28|NZ_CP045293|CRT matches to NZ_CP050096 (Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b3, complete sequence) position: , mismatch: 7, identity: 0.75

cgaacgctttgagcgagcggtgagccaa	CRISPR spacer
gctccgctttcagcgaccggtgagccag	Protospacer
    ****** ***** **********.

164. spacer 3.14|3210474|28|NZ_CP045293|CRT matches to NZ_CP050102 (Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b2, complete sequence) position: , mismatch: 7, identity: 0.75

cgaacgctttgagcgagcggtgagccaa	CRISPR spacer
gctccgctttcagcgaccggtgagccag	Protospacer
    ****** ***** **********.

165. spacer 3.14|3210474|28|NZ_CP045293|CRT matches to NZ_CP050107 (Rhizobium leguminosarum bv. trifolii strain 4B plasmid pRL4b1, complete sequence) position: , mismatch: 7, identity: 0.75

cgaacgctttgagcgagcggtgagccaa	CRISPR spacer
gctccgctttcagcgaccggtgagccag	Protospacer
    ****** ***** **********.

166. spacer 3.14|3210474|28|NZ_CP045293|CRT matches to NZ_CP018229 (Rhizobium leguminosarum strain Vaf-108 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.75

cgaacgctttgagcgagcggtgagccaa	CRISPR spacer
gctgcgctttcagcgaccggtgagccag	Protospacer
   .****** ***** **********.

167. spacer 3.14|3210474|28|NZ_CP045293|CRT matches to NC_017327 (Sinorhizobium meliloti SM11 plasmid pSmeSM11c, complete sequence) position: , mismatch: 7, identity: 0.75

cgaacgctttgagcgagcggtgagccaa	CRISPR spacer
gctgcgctttcagcgaccggtgagccag	Protospacer
   .****** ***** **********.

168. spacer 3.14|3210474|28|NZ_CP045293|CRT matches to NZ_CP016290 (Rhizobium leguminosarum strain Vaf10 plasmid unnamed3, complete sequence) position: , mismatch: 7, identity: 0.75

cgaacgctttgagcgagcggtgagccaa	CRISPR spacer
gctgcgctttcagcgaccggtgagccag	Protospacer
   .****** ***** **********.

169. spacer 3.14|3210474|28|NZ_CP045293|CRT matches to NZ_CP050112 (Rhizobium leguminosarum bv. trifolii strain 3B plasmid pRL3b5, complete sequence) position: , mismatch: 7, identity: 0.75

cgaacgctttgagcgagcggtgagccaa	CRISPR spacer
gctccgctttcagcgaccggtgagccag	Protospacer
    ****** ***** **********.

170. spacer 3.14|3210474|28|NZ_CP045293|CRT matches to NZ_CP021217 (Sinorhizobium meliloti RU11/001 plasmid pSymA, complete sequence) position: , mismatch: 7, identity: 0.75

cgaacgctttgagcgagcggtgagccaa	CRISPR spacer
gctgcgctttcagcgaccggtgagccag	Protospacer
   .****** ***** **********.

171. spacer 3.14|3210474|28|NZ_CP045293|CRT matches to NZ_CP050089 (Rhizobium leguminosarum bv. trifolii strain 23B plasmid pRL23b2, complete sequence) position: , mismatch: 7, identity: 0.75

cgaacgctttgagcgagcggtgagccaa	CRISPR spacer
gctccgctttcagcgaccggtgagccag	Protospacer
    ****** ***** **********.

172. spacer 7.3|5397552|29|NZ_CP045293|CRISPRCasFinder matches to NZ_AP018173 (Calothrix sp. NIES-2098 plasmid plasmid1 DNA, complete genome) position: , mismatch: 8, identity: 0.724

attcggagaaaaagtaggccaacctcgca	CRISPR spacer
tcaacgagaaaaagtaggacaaactcgcc	Protospacer
 .   ************* *** ***** 

173. spacer 7.6|5397604|29|NZ_CP045293|PILER-CR matches to NC_048807 (Erwinia phage pEp_SNUABM_01, complete genome) position: , mismatch: 8, identity: 0.724

gcaaattagctggaaagtcgctcgagaat	CRISPR spacer
gcaaatcaactggaaagtcgctcttcgtc	Protospacer
******.*.**************   . .

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	2699370 : 2735515	41	Brevibacillus_phage(23.81%)	tail,portal,plate,protease,holin	NA
DBSCAN-SWA_2	3001221 : 3010073	10	Staphylococcus_phage(50.0%)	NA	NA
DBSCAN-SWA_3	4914172 : 4931045	17	Enterobacteria_phage(25.0%)	NA	NA
DBSCAN-SWA_4	6309164 : 6324370	12	Mollivirus(20.0%)	NA	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP045293|2699370:2735515|DBSCAN-SWA
ATTATTGATCACTCCCTGCGTCATCGTTAGGTATCGGTGCTTGCTCGAATAACTTTGTCTGCTCTTCTTTCGTTAACACACCGTCATCTCGGTTATCAATTGGCGACGTCTCCGATGTCGTTGATTGAACTTCGTTCTGCACCACCGATTGAGGCGTCGTAGATGGTCCAAGTGTTAGATTGCTATAACGCATCTGCTGCTCAGCAAGTGCTGTCTCCAGCTTCTTCCGCGCCACCTTCGCGAGAGCCGTCTTCGCTTCCTCCACAATATTGGGATTAGTCTCAATCAATGCAAGCACTTCCGCATTCGACGGATAATTCACAATCGCGCTGGACTGCATACCCGGATCAACATAGGTTAGTCCATAGATGGAACCATGGTGAATCAATGCATCGACCATTGCGCTCGACATCATTAATATTTCCTGCTCCGTCAGCTGCAGGCTGATCGTATTTCCTGCGACTCGCTTCACTCGCTTCTTGGATAAGACAATATAATCCTGACCCGTTGGAAATTGGATACGGACATCAATGACATCCTGATCACGCAAATTCAGCGGTAGTTGGATCTGAGCAAATTGCTCATTTCGAAGATCATTCGGCGTTGCTTGCCCTTCGTAGAACATGGACGGGATAAGAACGGTATTCGCGGACAAGTCGATTTTAGATATTTTTCCAACAATCTTCTCTTTCGTGCCGACCACGTTCGCAGGAAGAAGACGAAGTTCCATTTCTTGCATTTCTACCTGTTGTGCTGAAATACGCGTACCTGCAGCAACATTGCCTTTTAGAACCCATACGTTCCCCATCTTGGCTTGCTGCTCCTGCCGTGCGGTCTGTAGTTCAGCGATTTGCTGTTCATATTGCTTCTCTGTATCCCGTTTGATTTTCTGAACGTGTAATTGCGAGTACACGGCATAACTTAGGAACAAACATCCCATGATGGCAGCGCCACTGAGTCCGGCAATCCATAAGTTTTTCGTCCGTTGTCTAATTTTTGACATCCCTTCTGCTCCTTCTTGAGAATAAAAGCTTACCGAGTCCTGTCCTCCAATTCGAATGCGTCTGTTCCATCGGCAGAATAGCCGAGAGGGCCTTTCGTGCCATATCGTCAATGTGGAATGGATCCACATGATACGGAATGGCATACAGCTGTGGAACGATGAAATTCTGTTCCATATCTCGAATCGTCTGCTGAGTCGCAAGGGGAATCAATCCTATGAAGCTGGCAGCTTGATGGGCGAACCCCGCTCGACGCATGAAATCGGATAAATCTTCTTGCCTCCACTCCGCGCCGGAAGCAACCACACACGATATATTGGCACGTAGAAACTCGGCGAACATAGCAGCATTGTCCCCATATACACCTAGATCAAGGACGATCACATCATAATCGGTATGGAGCAGAGGGATGAGGCTGCGTGATTCGAGATAAGGATAGTAATCGACGCCATGAATGGTGAAATGCTCTCCCGAGCGTCGGATGGGTTCTCCATCGAATATGGATCGAATACGATAAAAGGCTTCAGTCCTCATACACTCGACACATGCAACACGCTGATTGGATGCCGCTAAATAATGTGCGAACATAATTGCAGTATGCGTTGTTCCCACTCCGGAATCGATACCCAGAAGTGCAATTGTGCCTGTCCCGCGCCAACGATGCGTGGTTGATACAGGTTGATTCCCTCTCCATGTTTTGGCCATCTCCATATGAATCTGTTCCAGCTTCTCACGGACTTCCTGCGCCGTTTGAATCCGCAAATTCGGATCTCGATCTAACAGATGCTTCAGCAATTGCCGAAAAGCCAGTGGAACTTCTTGCGGCATCGCGTCCATCCCGGCTTGACCGAACTGACTCGTACGCCCTCCCGTTATCAAGTGCATCAATAATGCACCAAGACCGTAAAGATCGCTACGTGTATCGCTTTGCTTGCCTGTATACTGCTCCGGAGCAGCGAAACCAACGGTACCGAGACATACAGTGTCATCCTCCTGATTCGGCTTGAAATGTCTTGCGATGCCAAAATCAATCAACCGGATCTGACCATGCACATCCATCATGACATTCGTAGGCTTCAGATCCCGATAGACAATTGGCGGCTGGCATTGGTGTAGATATTGAAGCACCTCACAGAGCTGTATACCGAGCCGAAGAATATGATCGAAGGCTAACGATCGTCCCCGACGTTCGAAGTCGACAGCCAGCGTCTCCCCTTCGATATAATCCATGAACAAATAAATATACCCCTCTGCATCAGGACCAAGAAAATCGACAATTTGCGGTAAATTCGGATGATTCAATCGAATCAACATGGCCGCCTCCGCTGCTACGCCTGCCGCATTTCCCGGTTGCTGCAGTCTCGTCTCCTTTACAGCCCAACGCTTACCGACAAGCTTCAGATCCTCGACCAAATAGACATAACTCATCCCCCCTTCACCAATTTGTTTCATCACTCGATAACGCCCACCAAGCACCTGATGAATGCTTAGCCTAGACTCCCATTTCACGAGTCCACCTCCCTAGGAACAACAAAAAGGGAAAGCCTCTCGAATCATGACAATCGACACATCGGTCAATTCTCATGGCTTCGGGATGCTTTCCCTATCCATTTCATATTAAGTTGCATTGGACACATTATATATCATCTATTCCAAGATTGTCCATATGCAAATTTCATTTTATTGAATACTATTAATATTTCACCATGTACAACGTGATTTCATCGCGATTATGAACAAGCTGCTTCATGCGCCGAATTTCCAAATGCTCACTGAATTTTTCGCTGATATCACGTATCGTTTGCAGCGGCTTTTTATGCATGAGCTTGACGGTTACGATCGCTGTACCGCCTGATCTCAACGCGTACAACAAATCCATTACAAGACGCACCATTTGCATTGGACTCCAGCTCATGTCGCAGACGATGAGGTCGAATTGCGATTCGCGGAATTTCACTTCAGATGCATTTTTCTTCAGCACCGTTAGCCTACGATTCTCGAGCAATGAAGGATGCATTTCCGCCGGATCGATAGCAGTAACTTTTAAGCCCCGCTCGAGCAATAACGATGTCCATCCCCCAGGGGCTGCACCAATATCGAGCCCTTCAGAGAAACTCGCAAGATCCAGACCAAATGCTCGCTCTGCTTCTAACAGTTTGAATTTGGCCCGCGAGATTTGTCCTTCTTCCCGCTGAAACCGCAATGCCCCGCCAGACCAATCGCTTAGATTATCTTCTGGCGTCGAAATGCCGACATAAACGGTATCTTTTCCAGCAAAAATCGATACAATCCAATGAGAATCCCGTGTGACGGTTTCCATACCTGACTCGCTCAATCCCGCTTCCAACGCTGACTTCAGAAGAGCTAAGTCGACTGCGCCTGCGTCATTCGACGCTTTACGAAGCTGAACCGCAACCGATTGGCCCCGATGAAGAGCTTGATTCGATTGAACGAAGCTCAGAATCGCAGCGTTTCGTTCCTCTTGCCCCGCTTCCGCAAGAAGAAACTCTTGTTGAACTGGCTGAATATGACGTAAGAAAATAAGCGGATCCGTCTGCAGTTCACGGATGACCTGCGATTCATCCACCGGTAACGTCACCAGAATGACTTCGCTCGGAATAAGCACCATTGCTTTCACTTGTCCGAAACGGCGGCGTAACTCTTCTTGCGCGTAAGCAATAAAGCCATGATTGGCTGTACAGATCCATTTGGATGTTATTTCATGCTGTTGTTCTTGATGTTCAAGTTGTTCATTCAACGGTTATTGACCTCCAAGCCTTGCACCCGAATCCACGGCCGTCCATCTACCCATTCGAGTGAAAGAGGCACTTCGTATGCTTGTATTAATATTTCAGGGGTAAGTACCGATTCTTTCGTCCCGGCAGCTACCAATTTTCCTTGATGGATTAAGGCGACGTGCGTAAATAATGGTACGATTTCTTCCAGATGATGTGTGACGTAGACAAGTGCAATGTTTCTTTTCTTCAACAAGTTAATCTGATCAAGGAATTTCTCTCGCTCATACAGATCTAACCCTGCGCATGGCTCGTCCAAGATGAGGACTTGCGGGTCCGCCATTAAGGCGCGTGCGAGCATGATTTTCTTCCGTTCACCTTGTGATAAGGTTCCAAGTGGATTGTCCGCGACATGCCCTAACTTCATTTCATCGATCAGCCCCCGGGCTTTCGCAACGACTTCCTCGGGAATATCCTGATAGAACCGTAGAAATCCGTATTCCCCCGTAGCAACCACTTCCCAGACAGGATCGCGAAGCGTCAATTTCTCCATCAAGGATTGACTGATATACCCGATTTTTTTACGAACCTCGCGAATATCGCACTGGCCATATCGATTCCCCATCACATCAATCTGGCCTGAGCTCGGGAACATGTAGCCTGTCATCATTTCGAGCAGTGTCGTCTTCCCTGAACCGTTCCGTCCAAGGATCACCCAATGCTCCCCTTCATTCATTTGAAGCGTAATGTCATTTAGAATTTGTCGTTCTTCACGTCTCAGCTTAATGTGCTGCATCGAAATCATCGAATCACATCCTTAATGATGTTGAATAAATGTTCTACGGACCGCATCTCGTAGACTTGTACCGGTTCGCCTCTCCTCTTCGGGTCGAATAAGAATAACCCTGGGACGCTTCGTACGTGATACCTCGCCACGAGACGAGGGGAGAAATTCAAATTGATCTGTAGCAACTCGACATCCGGCAGCATTGCTTCAACCACATGCAGCATCCGCATTCCTGCCTTACACGTCCCACAAAGCGGTGTGTATAGATACAGACCGAACGGCCTGTACACGTCTACATGATCGATTCGATCGAGTAAATCTTGCTCATTGATTTCTTTCATGGGCAGCCTCTCGAATGCGCGTCAACACCGATTGCGGCATCGGGCCGTTATGGAGGATGACATGATCGGGTTTGTTCTGATAGAACAATTCATACATCGTCTTACGACCGGATAAACTGGAGGTATGTAAGTATATCTCTCGCGGATATAAACCTCGAAGCACCATTTGCTTCACTAGCTGTGTCCCATTCGGCTGATTGATGCCCAGATCATGATCCAAGGACAGAATATTGACGTCCGCTTCCTCCAGCAGCAGTAGGCATTCCTCAGCCGATCGCGCATAGACGAATCCCTCAGGACAACGGCGAATATCGTCTAAAAATACATGTATCATGCTCATTCCCCTTCATCTACCAAACCTACTTTTCTTTTTGACAGCTTGCGCAATAATACGTTTTTCGAGAACCAACCTCTGCCTTTTGAATCGTCGCACCGCAACGCTCGCATGCTTGACCGTCTCGCTCAATAACACGTACATGCGATTTATAACCTCCCGTGAGGTCATCCTTCGCGTTCAGACGCTCCTCGCCCATGCCGCCATATTCAATTGCATCGTGCAGGACCGTCATCGTACTGTGATACAGCCGTTCTATGCTCTCCTCCGATAAATCCTGTAACTTCGCTGAAGGCAGCAAGGCTGCTTCGAACGCAATTTCATCTGCATAACCGTTCCCGAGGCCTGCAATGAACGACTGATTTACAAGCGCAGATTTAAGCATCCCACGTTTACGAGCGAATAACGTCTGGAACTTCTCCAGATTCATTTTACGATCCAATAACTCTGGACCTAGATTACTTAGTTCTTGATCTGCTTCTTTTGCACTGAGAAGATGGATATACCCCTGCCGAATCCCCAGCAAACGAAGTGCCTGATCGCCAAAAGATATCATAACTTGTGCGTTAGCATGGCTTCCTTCATCCACTTCCAGTCCATTGAGTTGAATTTGCCCCGCTGCACCAAGGTTTAGCAGCAGTCGTTTTCCATTATCTAAGTGAAAGAGAAGCTGCTTCCCGCGACGCTCAATGAACAGAACTTCTCGCCCTTGCAATTGCTTGGACCAAGCAGCTGTATCACTATTAATCAGTTTATCTTCCTTTACTTGCACACCTGTGATCCGTTTATTGATAATTTGCTCGGAGAGCAATTTTTTGTAGGTTTCTAGTTCCGGTAGTTCTAACACGTATTTTCCCTCCATGTTGCGTACGAGATGATGAATCCAATAGGTAGGTATGTAAGTATTCTATTGCGCGTTTCTGCCTGATGTGACTGCAGCCGCCTCGTACAAATCCTTACAGATCCACGATGGCTGTACATCCGCTTGCGCCAATAATTGGTCTTTATTCGCTTCAGTCGCGAGCCCCGTCAACACGAGAATCGTATCACAGCCTGCTGCTTGTCCCGCGCGTAAATCCGTCAGCGGATTATCTCCAATAACAATCGCGTCTTGAGGCTCACATCCAAGCCTAGCGAGCGCGTAATTCATAATAATCTTAGAAGGTTTACCCATGACAATGGGTTCCTCGCGTGTTGCGGCTTGGATTGCCGCTGACAATGTGCCGGCACCCGGCATGATGCCAGTATCTGAAGGCAAAAGAAGATCGGGATTGGTGAGAATATACGCAGCGCCTTCACGAATCCATTGTACCGCTTGCGTTAATTTGGCGTAATCAAAAGATCGGTCGATCCCTTGCACGACGATCTCCGGTTGGTCCTCCGTGATCTCTACGCCGGCTTCGCGAAGTGCTGTCTCTAATCCATATTCTCCGATCACCGCTGCTCTTACACCTTGAGGGTAATGCTCTTGAATATATTGTGCCGCAGCCAATGCTGATGTGTAGACGTCCGCATGCGTGGCTGGAATCCCCATCTCCGCTAAATGCGCAGCAACATCCTCTGGCGTACGTGATGAATTATTCGTCACGAACAAATAAGGAATCTGAAGTGATTTCAACTCTTGAATCCATAAGTCAGCACCCTCTATACGATGCTTCCCATGATATAATGTACCATCCAAATCAATTAATAGTGCTTTGTTAGAATTCCCCATATCGGCCAGTATCCTTTCTTCAGCCTATCTTGAACACCCATGTTCACAATGCTTTTATCATAGCGAATTCATCGCATGCCTGCAATCCATTATACCTTCGAGCGAAGAATTCGATCGATCCACATCTCCGCATGCGCCGCATCCTTCATCGTCGGAGCAAGACCCTCATTCGCCCATGCATCTTCGCCAATATAACGGTGCAGGAAGTGATTCAAGGCACCAAAGTGACTATCTACGAATACGCCCATCGTTGTTTTGTCATTCGGAATCAGCTGTAGACTCGAGGGCACTGGAAGCGCAGGCGTCGCCCCCGACAACATGGAGACTTTCGGCGTAATGTCTTTCTCAAGATCGCAAGTGATACTTCCTCTGGTCCCAACGATCTGCACACTGAACCGATCCGAACCCCAAGCAATACGGGACACTTCACCCGTTCCTCTTACACCGCTTTTCGTCGTATAAAAGAAACTCGCCCAATCATCCACTGTCATTTGTACGCGCTCATCTGACCCTTGTGCTTTCGGACGTTCTTTGACGAAAATATTCGTCTCTCCGTGTACATCCGTAAGTTCCCCGAATAGATGGGCGATCAAATCAATTACGTGGATGCCCAAATCCGTAACGGCACCGCCGCCTGATATCGTATCGTCTAACCGCCATGAAACGGGACGCTCAGCATTCAAATATCCTGAACGCAGGTAAGAGCAATTGCACTGGAGAACGTCGCCAATGATCCCTTCCTGCAATATCGCCTTCATCTTCATAACAGCCGGGTGATAACGATAAACGAGTGCAACTTGCTGAAGCGTGTTTGCAGGAATATGATTCATTAACTCTTCCGTTCTACTGTACGCTTCTGTTAATGGTTTCTCAAAATATATAGCCTTGTCAGCGGATGCAGCAGCCGTCCCTTCCGTAAAATGCATCGCATTCGGCGTACAAATATCGACAATATGTACCGTGGGATTCGTTAGCGCCTCATCAAGACTGTTCGTCACCTGCTGAAACCCCATAGCTAATGCTTGTTCCCGATTCCCATCTGGGTTTCTGGTCACTAACGTGTCTAATACAGGCACAAAAGGAGATTTCTGAATGACAGGCATAGCACGTAGTGCGACAATATGGGTTTTGGCAATGGCACCGAGCCCTGTAAAAGCAAAATGTATCGGTTTCATAACGATATCCCTCTCTCTTATAAAGTATTTCCTATTGTAAAAGATGCGCAAACGATGTTGCAAGGCATCAATTCATGTCAAATCCTGCGCTTTCCCGGGAAAGTATTATATATTGCCTAGTAAAAGACGGAAAGCTTGTATGCGATGGAATGGATCGAACCGCATCAAGCTTCTTGGAACTTAGCGTAACATATAAATAACATATCCTGCTATACTCAGGAGGATCATCAATATCGCAATGACATTAAGAAAATTCCGTCTGTTGCCGGGGCTGTCGAAGCGATTTCTGCGGTGATCATCAAAGTCTGACATCGGTAAGCGACCTCCTTTTTCTACTCATTATGATTGCCCTGTGTGACTTCGCCTGTGGATCGGGATGAGCTCCAGTTGATTAGCAGCGATCGTATGCGGAAAAATCACATTAGCTTCCGCCACAAGCGGTTCGATATCACTATACCTAGCGCTGAAATGGGTTAAGACGAGTTGACCAACGGCTGCATCTCGCGCCGTCTCAGCTGCTTGTCTGGTTGTACTATGATAGAAGTTCTCGGCTAAAGACTCGAGTCCTTCCATGAAGGTTGCTTCATGTACGAGCACATCGGCATTCTGTGCGAGGTATCTCGAACCTGCACAAGGCCTTGTATCCCCTAGAATCGTGATAATCATGCCTGGAATCGGCGCTTGGATGAACTCATCGGGAGTGATAACTGTTCCGTCATCAAGAACCACATCTTCGCCCTTCTTTAACTTGCCATAGATCGGACCTGGAGGAATGCCTGCCTTCGTTAAGGCCTCAACATTGATCCGTCCCGGGCGATCCTTTTCCATTACCCGATATCCAAAAGATTCAATGCGATGATCCAACCTTGCTGCTTCAACCTTGCACTGCTCATCTTCAAAGACAATTCCTTCATCAACCTCTATAATCCGTATCTCATAATTGAGATGGGACTGACTTAATTGCAATGATGTCTTGAGATATTGACGAAGACCTGTTGGTCCATAGATTTCAAGCTTCTCCGTTCCTCCTTGATGGGAGCGACTGGATAACAATCCTGGAAGTCCAAAGATATGATCTCCATGCAAATGGGTAACGAATATTTTCTCAAGTTTACTCGGTTTAAGCGGCGACTTCAATATTTGATGCTGTGTCGCTTCGCCGGCATCGAACAACCAGAAGGTACCACGCTCGTCGAACATGCGCAGCGCAATGGACGTCACATTTCGCTCTGTCGTCGGCATCCCTGCACCTGTCCCTAAGAAATAGAGTTCCATAGCCATCCCTCCATTCTGCACCAAGAGCCTCCAACGAAATCGGAGGCTCTTGTGTCTTTATCTTATATTATACTTTCTCTACGTTAAAATATTGCGCTTGCGGATGGGCAAATACCATCGCGGATACCGAAGCTTCCGGTTCCATCATGAATCCCTCTGTCAATTGAATACCAATGTCCTCAGGCTTCATCAACTCGAACAATGGTCCTTGATCTTCCAGATCCGGACACGCAGGATACCCGAAGGATACCCGAATGCCTTGATATCTCGCACCATGACGTTGTTTCATTGTCATCTCTTGCGGATCCGGATAGCCCCAAATATCGCGCATCATGTGGTGAACCCGCTCAGCTAGACCTTCGGCGACTTCTAACGCTGTCGCTTGAATCGCATGGGATTTCAGGTAGTCCCCTACTTCCTTATATTTCGTCGCGAGCTCACGCACGCCATTGCCTGCAGTTACCACCAAGAATCCAACATAATCCATGATACCACTATCAACGGATTTAAGGTAATCGGCTAAGCATAGGAACGGTTCCACTTGCTGACGCGGGAAGGTGAAGGTATGAAGGACCTTCGTCGTGTCCTGCGGATCATAGATAATAATACTATCGCCAGATGATTGCGCCGGGAAGAATCGATACATGCCTTGCGCTCTAATCGTTCCATCCGTGATGGCGTTCTGTAATATTTCATCGACGGTTGCTTTTAACTCAACCGCCTTAGGATTTTTCTCTGCCAGCATTTGTTCTACCGAACCGCGTAATCCAAGATGATGCCCCAGCAGCATTTGCATATTTACATAAGGAATAATATGCCCTAATGGATAGTCGCGTAGAATATGACGATCGAGATCTGGCGGAATGAATACCGGTGCATCTTGCGAAATGTTCGAACGCACGGCTCTCGTGAGCTTCGGCAGCGGCTTCTTCTCCTCTTCTTCGCCTACACTTTCCTTGATCGCTGCAGTCTCTGCTATCATGAGCTGACGGTGCGTCGGATCCATAATTTTGTTCGCAAGATCTAAGCCGTCCATCGCATCCTTCGCATAGAGAACGAGCCCGTTATATTCGGGTAAAATACGTGTTTTGGTGAATTTCCGTGTCAACGCTGCACCACCAACCATAATCGGAACATCAATATTCGCATTGCGTAAATCTTGTGCGGTCAACACCATCTGCTGCGCCGATTTCACGAGTAGTCCCGATAGTCCGATCGCATCTGGCTTCTCTTTGCGATAAGCTTCGATGATCTGCTCAGGCGGAACTTTAATGCCTAGATTCACGATCTCATACCCGTTATTCGATAAAATGATCTCAACCAAGTTTTTGCCGATATCGTGCACGTCGCCTTTTACCGTCGCGAGCATGATTTTACCTTTAACCGATGATTCATTTTTTTCCATGAATTGCTCTAGATGAGCAACGGATGCCTTCATAACCTCTGCACTCTGCAGTACCTCAGCTACAATCAGCTCATTATTATTGAATAATCGACCAACTTCAGACATCCCTTCCATCAGCGGTCCATTAATCACTTCAAGTGCTGTGTACTTCTTAAGCGCCTCGTCCAAATCTGGAATAAGGCCTTCCTTGGTTCCTTCAACAACGTAAGATCCTAAACGCTCTTCTAACGTCAAGTTCGAAGCCTTCTCTTTCTTCACGACCTTCATATCCCGGAAAGCCGCTACAAAAGCAGAAAGTGTCGCATCATTCGTATCGTAGAGCAACTCTTCGGATAGGCGACGCTCATGCTCAGGGATCGAGGCGTAACGCTCTAACTTCTCGGTATTAACGATCGCGTAGTCAAGTCCTGCCTTCGTACATTCATACAAGAAGACGGAGTTCAGCACTTCACGACCAGCTTCCGGCAGACCGAACGAAATGTTACTAATGCCAAGGATGGTCTGACATTCTGGCATCGCTTCTTTAATGAGGCGAATCCCTTCGATTGTCTCTTTGGCAGAACCAATATACTGTTCATCCCCTGTCCCAACCGGGAAGACGAGCGGGTCGAAAATAATATCTTCAGGCTGCATGCCATATTTGTTCACTAATAGTTCACGCGAGCGCTTCGCAACTTCTAGCTTATCTACTCGCGTAATTGCTTGTCCACGTTCGTCAATTGTTCCGACAACTGCAGCAGCGCCGTACTTATGAATTAATGGGACAACATGTTCGAATTTCTCTTCCCCATCCTCTAAGTTAATGGAGTTAATAATCGCTTTCCCTTGTGAGTACTTCAGCGCCAAATCAATAACCTTCGCATCAGTGGTATCAATAACGAGAGGTACTTTGACCTTCTTCACGACTAGCTCCAAGAATTTCTTCATATCCTCGGCTTCTTCACGATCCGGATCTTGTACACAGACGTCAATGACGTGTGCACCGCTCTTCACTTGCGCTCGTGCGATTTCGGACGCTTCCTCGTACTTCCCTTCTGCGATAAGGCGTTTGAATTTACGTGAACCCAATACATTCGTCCGTTCACCCACCATGTAAGGCCGGTTCTCCGATTCAATATATACCGTCTCAATACCTGATACGGCTGGAGGGTGTGTTCCAAAAGCACTACGCGGTTGGAACTGACTCATTGTATCCGCTAATGCACGAATATGATCTGGCGTTGTTCCGCAGCATCCGCCTGCAATATTCAGCCAGCCTTGCTCCGCGAACCCTGCCATTTTCTTCGCTAACGAATCCGGGGATTCATGATAGTGACCATTCTCATCTGGTAACCCCGCATTAGGGTAACAACTAATTGCCGTATCGGCAATTTCAGATAAAGAACGAATATGATCACGCATAAACTCTGGGCCTGTCGCACAGTTTAACCCCACGGAGATTGGCTTCAAATGCTCCAATGAAATATACAAAGATTCGATGTTCTGACCAGCAAGTGTCGTACCCATCGGTTCAATCGTACCTGAGATCATCAGCGGAAGCGTCTTTCCCGTTGTCTCAAATGCGCGTCGTATGCCGATACTTCCGGCCTTCACATTCAATGTATCCTGCGATGTCTCGAGCAATATCGTATCAACACCGGCTTCAATAAGTGCAACGGTCTGTTCATAATAAGAATCGACAAGTTCATCAAACGTGACTCCACCGGTTACGGACAATGTCTTCGTCGTCGGTCCTAACGCACCCGCAACATAACGCGGCCACTCCGGTGTTGAATATTTATTCGCTGCATCTACTGCGAGCTTGGCTGCTGCCAAGTTCAACTCTCTTGCTCGATCTTGCAAATCATATTCTGCAAGTACCACGCTCGTGGCACCAAATGTATTCGTCTCCAAAATATCCGCGCCAGCTTCAAGATATTCTTCATGAATCTTCTGGATCACATCCGGTCGCGTTAGAACAAGAATCTCATTACAGCCATCAAGTTCTTCGCTCCCAAAATCATCCGCCGTTAAGTCTTCACGCTGAATCATCGTTCCCATTGCGCCGTCAAGGATAAGGATTTTATGTTTCATTTGTTCTTGTATGCTCAGCTTATTCATGCCCAATCCCCTTCCTTCTGCAAAAACGTTAAGAATTAGTTTAACAGAATACCAATGTTTAGAAAAGTGTCAATGCATTAAAAGTCGACAGCCAGCTCAAAATCCACTATAATACAATCAAAATCAAGTTAATTTATAGGAAAGAAGGGATTAATTTTGGCTGAAATTTACATTCGTAATACAAAAGAGCGTATTTCAGGTGAAGAAGACGTTCGTGCATTTCTAGCGAACCAAGAAGTATTATATGAGCATTGGGATCCAACGAAGCTGCCAGAAAACCTTCGTGAACGGTTCGTTCTCTCCGATGAGGAGAAAGCCGAAGTTCTCGCGACCTATGATGTAGAGATTCGTGACCTTGCTGCACGTCGTGGCTATCAGATCTGGGATATCATTACGCTATCCGATGCAACTCCGAATCTTGAAGAACTACTCACAAAATTCGAAGACGTCCACACGCATACGGAAGATGAGATCCGCGCTATCACGGCGGGAAAGGGGATCTTCATCATCAAGGGAAAAGACGACGTAGGTTATTTCAACGTCGAGTTAGAAGCTGGTGATGTCATCTCCGTTCCTGAGCACACGCCGCATTTCTTTACGCTCATGGATAACCGTCAAATCGTTGCTGTTCGCCTCTTTATTGAGAAAGATGGCTGGATTGCTACTTCTTACGATGACCCTGCGTTCCAAAAGGCCTAATGAATTCATTTCTGCGCTAAATATTCAAAGCCCGCTTCGTCTTCTTCAGACGGAAGCGGGCTCTTCTTGTTTATTTTGCAACTTCGAAAGTTTTCTTAGGCATGGAATGCATTTCACGGGCTGTAACATGCGCGATCATCGTATATTCCCCGGATTCTGCGAACTGCTTTTCAATTTGATATACGCCATTACTGGTAAGTTTCGCTTCAATTTTCTCATGTTCTTGTTCTTCTCCACGCCATAGCTCAAACATGACTTCCTTCGCATCATCGACAGGTTTGTCCGTTTGCGTTACTTTCGCTTGAAGCACAACATCTTTATTGGCGGTAATCTGCGCTGGCAGAATAATTTCTACTTTGATCGGATTCATGGCATCTTCGCTCATGTCCATATCCATGTTCATGCCGTCATGATTCATACCCTCATTCGATCCTGAACAACCTGCTAATAAAGCGATCAAGAGGATACAAGCAATCGCAAGCATACTCATCTTTTTTCTTTGCATGATTTGCATTCCTTTCTAATCTGCTTACTTGTTCGTTAGATTAAGTCTTTAACATCCTTAATGATTTGATCGTATGGAACATCTTCTACGCCATCATACTTCTTCATGATATATCCTTCTTTACTTACCAAATAGAACGATGTGCCATGAATCATCTGATCCGAACTAGGTTCCTTCTCTACAATCGTCTTAAAGGATGATTTTGCGAAAGCCTGAATATCTTCTAGCTTGTAATTGGTCAAGAAATGCCAGCTCGCAAAGTCAACGCCGAATTTGTCAGCGAACGCTTTCATAACCTCCGGCTTATCTCGGTCAGGATCAACACTAAAAGATACGAATGTAACGTCTAAGTTCTCAGCTTTCAATCTCTTCTGAAGATCCGTTAAGTTGAACGTCATCGGTTGGCAAACGGATGTGCAATTCGTAAATACGAAATCAGCGAGCCATACTTTACCTTTCAAATCAGCAAGACCGAACGCTTGACCCGCTTGATCCGTATAAGCGAAATCGCCAACTTTCATCGAGCTTGTCTGCTTCGCTCCACCACAGGCAGTTAATAACAGCATAACCCCAAGCATCAAGAACATTAATTTTTTCATTTTAACCTCTCCTCTATGTATCGCGGAACAAATTTCCTTTTTCATTATAATTTGATTGTACATGAGAAGAATGACTCATTCGGGCTATCTTTGTCAATTCTTTGTGACGATTTTGTATCAAATGTCATAGCCGAGCACAAAAAAAAGCCCTTGTTCCGATTTCGGCAACAAGGGCTACTTCTTACTTAAGCATGTTGATTAATAATATTGTGTAGTTCCGAGAGATGTGTGATTTCATAATCTGGAACAATTTCATCCGAACGTTGGACACCATGTCGATTCACCCAAACAGCATGCATACCTACGCCTAGCGCACCCTTGATATCCGTCGTAAGCTTGTCACCCACCATAAGACCTTCATGAGGTTCAATGTCAAGCGCAGCCATCGCATGTCTAAAGATAGAAGAAGCTGGTTTACCTTCGCCGAATGCCCCTGAAATCACAATATGATCAAAATAAGGAATAATGTTAGGAACTCCGTTCAACTTCTCCTGCTGCAGGTCAGGTGATCCATTCGTTAATAATAGAAGCTTCACATTCCCTCTCAACTCGTCGAGAATTTGGAACGTCTCCTCATAGACATAAGGACGAGCCCGGCGTTCAGTCGCGAATAATAAACCTAGACGCTCGCCGAGCGCTGCATCTTCGACACCTAACGCTTGTAGACCTTTTGTCCATGCTTCCGTACGATAACCTGGCGCTAATGCCTGTAATTGACGAAATTCTTGTTGTTCCCCATGTGTGAAATTCGCCCACAATCCTTCAAAAGGATTAATCCCGATCATCTGCGTGAAGGGGAACGTTGGGTACGTTTCATAGAGGGCTCTAGCCTCTCGTCTCACCGCTTCTTCCAACGCAGTAGGTTGAATGTGAGGATACGCTTGCGCAGCTGCAACACATGTCGCTTCAAACGATTCCTTCACACTGCGATCATCCCATAATAAAGTATCGTCCAGATCGAATAATACGGCCTTAATCGTCATCTCTCTTCTCCCCCATACCTTTACAGTGCTCTATCCTTAACGTTCTTCAAAAGGAACATGATTAACGCGTGCAAACTCTTTCAATCGCTCACCGATCACTGCGGTCTCATAACGGTTCATTAATCTGGAGAACACCCAGTTGGAGCCTTTAGCCTTTGGACTAATAACGACATAACCTTTTTGTACAGTAATCTCTTTGATTTGACTTGCATCCAGCCGTACGTCTCGATTGAAACGACGTGTCCCGATAGAAGATTTACCTACGCTAATATAGGGTCTACGAAGGAAGATCACAACTCCCAGGAATATGTATAAACCTACGGTCCCCCAAAATAAGGCTGGCGAGGTTTTTTGATCTACTGCAGAATATAGAATTGCATACAATAAACCGAATGCAACTAATGTAATTGGCAGAATCAGATTTCGACCAACATACCGATCCACATCTGATTTCGCTTCTCTACTCGATCCTATCATTTGTTGCCCTTGCTTCTTACGAACCTTATTTACATTCTTCGTGTTCTTACGCACCATTCTTTCCCATGAGCGGGCCATCCAAATCCTTCCTCCTTGGAAGTTTTCCCGAAGGAAAACTTGCTTCATCTAATGTTTAATTGTTGGATTATTATCATCCTCATCAACAATCTCAATATTATCGAGCTGTTGCTTCAAGGAACGTTTGAACCCATCAATATATTGTCGACGAAGCGCGTCCCGTTCAACCGTCTCTTCCGGTGTCAATCCTACCGATTTATGTTTACGAGCCAATTCATTAATTCGCTCAACAATTTTTTCGAAATCCATCCCTATCCCCCCTATTCTGTCCTTATTACTTTGACATTTACAATAGAGGTTGTCAAGGGTAACCCGTCCGCTCCCAGCATGTGCCTATGCCTTACACTTGCATACAATTTATCCTTTAAGAACTGGTAACTTAATCACTTCACCAGATTGAATAGAACTGTTACGTTTACCATTTAATTCTTTGATCTCTTCAATATAATTACGAACATCCATTCCGTCTGGCTTATGTTCCTTCGCGATCGCCCACAACGTATCCCCCGGAGAAACAACAATCTGAAGCGGTATGTTCGCATTCCGTTCCCCATCACGTGTATCCGCAGCAAAAGCATTCAATAACCCCATACTCGTCAAGCTGCATACAAGAACTAAAAATAACACGACCTGAACGACCTTCTTCTTAAGGAAAGAGCCTCTATTCACGACTTTGGACTGGTTATTATAAACACTTTGATATGAGCTATACTTTAGCATTTTCAGCACCCCAAACGTTTGTTCTGTTTTCTATGTCCATAATTTAACACGAACATTCGTTTGTGTCAATAACTTTTTAGAACATTCGTTCCCCTTGTTCGTATATTTTAGAACTAATGTTTGTACGAACGGTAGTTCTATGCTATAATTTTGTAAAAGTCTACTAATGGAGTTGAACCTCATGTCTAAAATATCCAATAGACAACAAGCTATTTTAGAATTTATAAGGAATGAAGTACGATCTAAAGGTTACCCTCCTTCTGTTCGTGAGATTGGAGAAGCTGTCGGTCTAGCTTCCAGCTCCACTGTGCACGGCCATTTGGATCGACTAGAGAAGAAAGGCTTAATTCGCCGCGACCCTACCAAGCCGCGGGCAATCGAGCTTCTGAGCCAAGAAGAATCCGAACATACGCATCTCTATACGCAGATGATTGCGAAGGTACCAATCGTGGGGAAAGTTACCGCAGGTGCACCGATTACAGCAACGGAGAACATCGAGGATTACTTCCCGCTGCCGGAGCAATTCGTACATGACCAGAATGTATTTATGCTTTCTGTTATGGGTGAGAGTATGATCGAAGCAGGCATTCATAATGGAGACTTCGTTATTGTACGCCAACAACAGACAGCGAATAACGGCGATATCGTCGTCGCGATGACGGAAGACGATGAAGCAACGGTTAAGACTTTCTATAAGGAAAAGGATCACATTCGACTGCAACCTGAGAATGCAACGATGGAACCTATCCGATTGAATCATGTGACTATTCTAGGCAAAGTTATTGGTCTTTTCCGTAACATGCACTAATCCGCCCTACATATTAGCCGTGTTGTTTAAAGAGCGATGCGCTAATTCCTATAACATTCGTTGAACTAGGACATGTTTAACGACAACCAAAAAACAAGCTGGTATCTGTATCACACAGATCTCAGCTTGTTTTTTCGAATCATTGTGGAGCCTGCCCCGAAGCTTTTCGCAGTTCATTCGCTAATCGATTCGCTTCTTTCTTTCCTGCCTCGTCCCCTTTTTGCTGCGCTATTTCCCAAGCTGGTTTTAGATACAGATCGATTAATTTATTGGCATCTTCCTTCGCTAACATGACATTCGCCTCCGTTTCAACATACGCGATCCCAAAATACTGGCAGACACCTCTTGCAATTTCTTCAGCACATAGGTCTCGATATGCGTCCGACAGCAAAAGCTTGGCTTCTTCCATGTTATCCATAAAGCCGCACTCCACGAGGACTGCCGGCATTGTAGATTCCCTTAGCACATGGAGATTCGCCGGTTTGACGCCTCTGTCGCGGAGCTTCGTGCCTTGGACCAACCTTGCATGAATCGCTTCCGCAGCTTTCATGCTGGTCACACGTCCGGGATAGTAGAATGACTCAATCCCATTCACACTCCCCCATGTCTCTCCTGCTGCGTTCGCATGAACGGATACATAGAGGTCTACACCGGATTGATTCGCTGTGTCCGTCCGGGTCTTCAGGGGAACATCGCTATCTCCTGGCGCCACGAGCAATGTACGAAAACCACATCGTTGTAGGTGCTCGTCCAAAAGAGCAACAACCGCACGGTTGAATTCGTTCTCGTGCATAAATGGCTCACCGGTTTCTTTTGACCGCGTCCCATCCTTGAACAAAGGCGTCCGCTTACCTGGCGGTTGCATTCCATGTCCATCATCTAAAGCAATAAATAGACTCAATTGTCTTCACCTCTCTTCCTACTCTATTAATATGCATCAATAGAATTGAAGCGAATGATAGATACCATGGTCTAAGTAGCCTGACTGCTTTCTATATCGACTGGGCTGAGGGTTTTGTAATGCACTTATAAGTTCTATCTGAGGACCGTTCACCACAGTTGCATTGGCTTATGTGACAAATTAATCAATTCCTCACATTTTAATGTAAAATCATGCCACTTTTTCACTTATAATAAGGTCTAATGAATAGGGGGGGATACCTTGAATAAGCAATTTATTAAAACAACCGCAACTCTTTTCATCGGCATGATGCTCGGTACTGTTACAATTGCAGCAGCTGCACCGGAAGTATTCCAAGCTTCCATTGCAAAGTTAAAAATCGTTGTGAATGGAAAAGAGCAAAAGCTTAAAAATTCACCTTTGCTCGTTAATGGCACTACATATTTACCAGTACGTGATGTAGCTGGTCTATTGGGAGCAAATGTTGATTTTAATAAAGGCACGATCACTATTGCTCAAAAAAAGGTCCAGCCAACTGTGAATACAATAGAGTCAATAAATGGACGGGATCTTGTTGAGATCTTAGGGAAAAAATACCCTGATTTTAAGATCTCCCTTTCTAATGAGGGGCTGCTTAAATTAGGCGATAACATCATTCATTTAACAGTGAATGATGACTCGACTCTCAATGTCACTCCACTTAAGGATTCCGGCTTTATTTCTAAATCTGATCTTTAGTAGATTCCGCTACCACGACTTTACGCGAAAAAATTGCGTACTAATGTGACTACACGCCCCAGTTAATTCACTGGGGTTATTGTTGTTTCTTGAAAGTTCCTCGTTGAATCTTTCCAGAACTATCATTCGAAAGATAAGGGAACCAACATCGAAACTTGTTCCATACTCACTACTACCTTGCCATCAACTTTTACATCCACTGTTGATGGACAAATATGAGACTCATCTTCAAACCATCCTCGATAATTAATTATTTGTGGGTGCTCATGCCCTCACAACCATCTCGCGAAAAATACCCACACAAACAAAAACCCCCGACGCATACAGCGTCAAGCTTAGTATAGAGTAATGTATTGATCGCGTTCCAATAGGTGGACTTGCGTGCGATAGTATATTATGCCGTGTTATTCCTTATATTATATGAAGAAAAAAATTTAAAACTTGGCTATTAAAGGTTCTGAATTGATATGTCTGGGGGCATTTAGGGGGTGACCTTGGGGGCACATTATTTAACTTCAAATGAAAAATAGCCTCGGTTTTCCCGAGGTTATTTTATTCCTATAATTTTGAAAATGCTGATATTTTCGATCTTACATTTTTAAATTAACTGTCCCATGTTGTTGATCAACACAGTCACGACTCCACTTAATTCTTCATTTATAATCTCATTAAATACGACCAAAGTTATCTTGGACCCTATGGAATATGATTCTCCTAATGCTACAGCAATAAACATCTCTTGTGGGGATGGGTGACACTCTTAATGATGCAGTACAATTTTACTATAGTGGTGGAAGCCATTCGGTAGCATATGCATGAATAGATAGTACTTCGGATTATGATTATTATGTTATCGATAATATAGGATCAAGTGATCCTGTAAGATATGCTCTAACACTAAGATCTCCCGCAGGAAAAAACTATGACATGCAGGTTATTTTAGTTGATCCAAATTGAAATATATTTGACTCGAAGTACGCCACTATTGACGGTGCGGGTGGTACTGAATTATTTAATGGAATCTCTACAATGTGCGGTTGGAGAACATATGTAAAAGTATCTTCTCAACTCCGTCTCAGTCCAACCGTATGATGGCGAACCTTCTTCCGAATCTCGTAATGCAGATGTGGCCCTGTGCTCACTCCCGTCGAGCCTTGGTGCCCGATCATTTCCCCTTTACCCACTCGTTGCCCCACTTTGACCGTGATCATGCTCAGATGAGCGTAACAATGCAGGAACCCATATTTACCCTTGATTGCTACAACCTATCTCATGTTTCCGAATCCAGTCCCTGGCTTACCGAGTGAAGCGTGTAATACTTCACCTGATACGAATGCATATATCGGACTGTTGGCGGGACTGACTACTAAATTAACGCCACGATGGAATTTAGGAACCTTGTATACTGAGTGAATCCGCGATCCGAACGGACTGGTTAGTATATTCATCGTACATTCCCGTTTCTAGATTTAGCACGATCGACTTTCATATCAGTTCACTCTCGACCCATTTAATGATCTAATACCTTTTGTGGGAGCCAATCTGCCCAGCCGGCCCATACTGCATTTGCCGTCATCGACTGCAGCGTATGATACAATACCCCAACCGCTAAAGCACCGAATATGATATCCGGGAACCCGAATACTTCATCTAGCAAGTGGCCGGCAGCGGGTAGCAGCAGAATGAAAAAGGTTCGAACCACTCCGTCAATCCCATATTTACTGGCGTATGTTCGATCCATCTTTGCAGCCCATACACCCGTGATCCAATCCATCACAATAAAGAAAACAAGTGCGATCATCAAGCCACTTGCCATTTTGTTACCTCCATAGAAAAAATTGAACACCGGCGCACCGATCGTTCCCACAATTAAAGCCATGATTTTTCCATTACCTCAATCCTCCTCAATGTAAATAGCCCCCGGAAACCCGAGGGCATAATAATAGCGCCAACCTTATTGGCGGCGCTCAGGCAGTGATTAAATCTTCTTTTCCTTTTGATTTCAAATAGGTGTCGATTCCTGCTTTTAGGTCAGGACGCTTGCTAATTACATAATCGTACTCCTGCGCCCCGTCAATAATGCGCTGTGCCATATATGCCACCATTATAAAGTCCCTCCTAAAATTAAAACATCTAGTGCGGATTGCATTAAGTTCTGTTTGGTTTTTAAAGATTCGTTTTCTGCTTTTAGCTTATCTATCTCTGTTGGATCAGATACAAAATCACGCTTAGCAGCTTCACTAAAAATTTCAGCGGTAACTTCTTCGACATGCTCTTTCGGTGCTTGTGTTACTTTTTCATCAATACAGATATAAGCAACTTCTTTTCCATTTTCCATTCTAGGAAAGCCGCCTAATAGCTGATCAATGGGAACACCTCCGTAGGTATAAGTAATGGAAGCCCCGATTTCAATCTTAAAATTATCTGTTAACCTGTAGTATTTTACGTTCATATTAATTCCTCCTAATATAAATTCCCTGTATAAATATACTGACCGTATGACTGAGGCTGGAAAAGCACCGTACTAGGTGCATTCATACATAAATATTTCTTACCATCAAGCCCCTTAATCATCGAAGGAGGGTCACTTCTATTAAACATTCTATCGTAGAAATTAGTAGTAACCTTATAATGGTATTGTATTACACCGTTAGCAGTAATGATCATAGTTTGCAAAGGGGTATTCTGATTAGAAATCATAAATTTACCTTCGCACATCGCATATGTCATAGTACCAGAACCCCCGCCGATCTCGTACTCATATGAACCAGAATAGTTATTTAACAGAACCCCTGCTGTATTGTAGATTGATAAAGTGTATGATGTAGCTCCTCCGATAATGGTATAAAACTTATCGTTATAAAATTGACAGTCATCGTTACCTATCTGGTATCCCTTCACATTTGGGACTGTGCCTAATTCAGTATAGTTCCATCGGTTATCTCCAGCTGCATATGAAATTTGAACTTTTCTTAGATAATTTCCTGCAATTGATCCACAATACCACGTTGTATCATATGCATGACCTTTTGCTCCTCTTAATTGTTGAATTGCTCCATTGTCATACTGCCCTGCCGGAATTGAAAAGAATTCATAAGAATTTCCGTCCCCGCCTATTTGCCATACCTTTGCAGTAGAATTAGAGCTGTCATAAAACCCAAATAACCCCTTATTAACATCGAATCCCAAAGGCGCATTGACCATTCTCGACGTTAAAGCTGTCAATCCTCTTGGAGTGCCGACGACTTTAAGCAGTTCGTTTGTTATTTGTGATTGCTCTGCTGTACCTACCACCCCAAATATACTCTTTCCTTTAATAATATTGGCAGGAATATAATTAGTGTCTGACGCTATCAAAGCACCGTAGCCGTTGACGTTTTTACCCTGTTTGTAATAGCCTGTTGGCGGCTCCATTATAAGGGAAGTCATGCTGTCCCCTTTAGTGCTCAAGGCGAAAACATACCCACCGTTATTGGGATATGCAGAATAGTCAGGCATCGTCCCCGTCAACTGTACCCCAACATCATTCGTGAATGTCTTAGTGGCTAATACATCTGCTGTAGTCGCATTACCCGATCCCCGAATGATCTGCGAAATCTTATTGACTAATGCCGTAAGAGTCTCGGATGCCGACGCTGCCACGCCCTTCGCGGTTAAATTTGTCGCCGCTGTGGACTTAATCGTGTTGATCTTACTTTCCATTTGACTCGCATCATCGGTTGCAGAAAGCGGCGCGCCAATAGCCCCTGCAACCTTGGATTTCAGGTTATTGGCAAGCGACTTTAAACTTTTTAATACCGCGAGTACCGTTTTCTCTGTGAAATCAGTATCGTTCACAGCAATCGCCGATGCGTCATGCGCCGCTGTTGTCTTGTTTGCGTGATTATCAACTTTTGTTTGTGCACCTGTGGTCGTTTCTTTGGCGTTCCAACTGGTTTTCTCTGCGTCTGTGACAAGCCTATTATTAGCATCTTGTACTAGGATACTTGCTGGATGCGTTGCGGGATGTACGTACTTATTCGCCCCGGCCTCGATCCCGTCTAACTTCCCTTTATCCTCTTTTGTCATTCTCCCGTCAGCTGTACTAGATGCCTTTTTGACTACTTCTGCGTCCAATGTATCCATGTTTCCGTTAAGGTCATCGATATTGACAATATCCGTACCCTCTGGTTTTTTCAGCCCCAAATTAGCGGTTGTCTTCATTCTCTCACTCTCCCTTATATGTCCTTAGTTCGCCCCATGATTTGGTGTTAGCTTGCTGCCAAGTCAGACCTTTCAATGTCTCCCACCAAGTATACGTGTACTTGAATGAGTAGGTCAGATGTGCCGGCTTAATTTCTTCTAGAACCTGTTTAAGTCCAGCCATGTTGGGTGGTATCCCCATTACACCAATAAACTGTACCTCGAACCGGTGTTCAGATGGATACTCGACAACTTCTGTTTCTCCACCACTAAAGGCAGCTGCTACACCTTTAATCATCTCTTTTGTTGTAGTCCCTGATCCTCTTAGTTTAGCCAATATCATTTCTCGTCTGCGCTCATAGGGTTTGGTATTGTCAGTTGTGAGGCCCAGCTCTCTTTCCCAGTACGCTAATCCCCAAGTTGCAGTTTGAACAAAGAACTGGTTGCCGAGTTCACTAAGCGCAAACCTTGCGGATCCAATTTCTCTAGCAGCTACATCTTGGATACATGCCATTTCAGAAATTTCATGCCAGTATTGTGGTAGATATTTGAGCAGATCGGGTATGTAGCCGTCTATTGGGTCTTTTCCCTCGACTTCCGCCCCGAATTGTAATGATCCGTATTGATATTGTCCGTACATATCACACCCCCTTAAGCTGATTCCATGTAAGAGGCCCTTTTGACATGAGTTCCGGTTTACCTGTGATACCAGTCCACGAGACGGATTCAGCCACTTCCGCGATATCTACTTTGCCATCATTATCCGTATCATATATGCTTTTCAACATATCCCCGGCTGTCTGAGCGGCCACTAGTAACACATTGCCGGAATCAAATCCAATGTATAATTTTTTTGTATCTGTGCAGAATCCCATTTCTCCTAATGCAAGTTGGCCAATATTTGCTTCAACACCTCGGCGGATTTGTATCAATGCTTTTCTAGGCATTTGTCATCCCCCTAAAATGTGCCGCCATCAACGATAGACACCATTAATTTATTCCCATTTGCAGCATCATACGAAATACTTGTGCCGTCTATATTCGCGGCAACGCCGTTCCCATCAACAAGTACGCCTTTACCGGCCTTCACTGAAACAGATTCCGCCGCTACAGTGATACCATTGCCCTGTCCTACAGTTAGTGTCACGGAATCAGCTTGTCCTCCACCCGTTAAGCCATTCCCTGCCGTAATGGTCTGGAGCGCACCACCGGTTCGAACCCATGATGTACCATTCCAGGAGTATATCTTTTGCTCATCATCTACATAACACGTCCAACCAACCGCGGGAGGATAATACATCCATGTTCCGGACTGCCACTCTGCAATTTGATTCTGTTTGCCTGCCCAAACACCGGATGCACCCGATGGAATAACGTACCGATCAGCTTCAATAGGGCTTGCAGGTGGGGCTGCTGTAGTACGGTTTTTAACCGATGCCTGCGGCTCAATGTTATGCTTTGCTAATTCGATTTCATTTTTAATTTTTTGCGCTGACCACAAATCAACTGATGATCCACCCGAATCGTTAATTACACGATGTTTCGTTACATCATCAATATGAGTCTTTATTTCAGCTGCTGTTTTGGTATTTATTCCATCCGATACCTTATTGACTTGTCCATTTGTTATTTCCGACTTTTTCACCCTTGCATACGTAGTGCCATCTGCACCATCATCAATTGTCCCTATTAATTCAGAGATTTTTTGTGCATTCACACGCTGCCATGCAGTTCCAGTGTCAAAGTACAAATATCCTGAGTTCGTTCCGCTTGTTACAAAATAGAACCTACCAAGATTCGCTGCAACTGGTCGCGCTGCTTCCGTTCCTGACATCGCTCTACCAACAAAGTTATTTACTGCACCATCCCCAATGAATACCTCTTTCGTATCCGTACAAAAGCCCATTTCTCCAGTCAACAATGCTCCTAATGCGACTAATTCGGCCTTATTGCCTCGTCGAACTCGTATTGTTTGCTGTGCCACTATGGATCACTTCCCCCTCGCAAAATATCCGCCATCAATAATCCCCACTTCTTTGTACCTTTCTAGTTCAGCCTGAATCGATATAATGCTAGACTGTAATTGGTTAATATCATCAGCTTCTACAATATCCCCGTTTGTTTCATAAGTAACATAGACCTTCGAAACCTCCGTATAAATCTTGATTGATCGACGCCAAGGTGTATCGGCTGGAACGGATATTACATAGTCTGTGATTTCCTTGCCGGTTAACTTCGGTCCGGTATAAACCCTAATACTGTTATTTGTGATGTTATCGTGAGCGAGTAACCCCTCAAATGATCCTCCCGCGATCACAAGTATTTCTTCAATCACATACACGCTGCCGTCTAACTTTTTATTAAGTTTCTCCGTAAATTTGTCCACTTGATCGGGATAAGACATCTATTACACCCCCAACTCGACTGAACCGAAAACAGGTATTTCTTCATCAGCCAATGGGATGTTGACTGTCCCTCCGTTTAATGACATAGCCGAATAATCCAATACGCCGGGCACACTCATTAACAACGTACCTATTCGAGCATAGCTAACATACGTCATCTCAAATGCGATACTCTTCAAATAATCCGTAAGAAGCGATTTGAAACCCTCGGTTACACTTTGTAATGTGTAGCTAGTTGCTAAAGCCACTTTAGCCTTCACTATGATTGCTTTGCCTACACCAGACACAACGGTCACATTCGCTCCAATCGGACGTACCTCCTCGATATAATCGGATGTCTGTGCTACCGAAGCAGGGTCAGCTGGTTTTTTATCCAAATCGGCAATTACGACCTTAACGCTGCCCGGACCATTCCATAGCGGAAAGACTTTCGCATCCCCTACACCTTGAACTGTTATCGCCCACTGCTTATATTGATAGGCATTTCCTGAAGTCGAGGCCTGCTGGACACGAAGCTGATATTTGGCTAGAAGCTTCTCATCGGGCTCCTCGTTGACCCCTTCTTGTACGATGTCGGTTAACACTGCACGCGTGAGTTTTGGCACATAGTCTACGGGTAACAATGGGCCAATTGGGGTATTGCCGACATTTCCAGCAACTTCACATTCCAGAATATAAATTCCTGGATCGATCCGATCCCGCGCGACATACGTCACATCATCTATTGAGAACCGACTACCCAATGGGACATCCAAGTACTCATTACCTGAATAAAAAACGCCTTGACGTTTGGCCTTTGTTGCCGGATTACGTGAAACACCCATTTCAGCTGCACGTAACGCAAGGTATTCGCCGCTTGATGTGGATGCAAATGTTAAGCGTAGAAACATGTCTATGTCCATATACATCTGAGCCATTTCCGCTGCAGCTGGTGCCAACGCATCATAAATAACGCTACCAGGTCGCTTATCGACGTCATTGGTAACCCGATTGAGCATGCGGTTCAAAATAACTTCAAAACTTTGTGCTTCATACATCTCTTATCAACTCCATTCTGAAATCGCCATAGGTGGATACGACCGTGAAATCCACTAGAGCTTCATCGCCTTGGACAATGATCTGTACATCGGTAATATCGGATATCCGATCATCCTGCATCAAGGCCTCGCGAATTCGACGTTCCAGTTCAACGCGTAGAACCGCTTCACTTTGACCGATCAGATGATTCCCTTGAAATCCATACCAGTTGCCATAAATGAGATGAACGAATCGCTCCGCGTTTAGAATTTTATAAACTGATTGCTTGACAGCATCAATGCCCTCCGTCATGCCTATCACGCGTCTAGTCCCAAAGTTTATTTTGTAAGTTCTGCTCGTCTCAACCTTTTCCTCATTATGAGGTTCAATATCGCCACCAATCGGAATCACGTCGTCACCACCTTGTCCCACACCACATATTTTTGTCCGCCTTGAATACGCAATAGGATAACAACATCCCCAACCTTAAGTCCTTCGCGGATAATTACTATATTTTTCATAGACTGTTGCGTTTCCGTTTGGGTATTGCCACTCATATTCACATACGCAAGTTCTAGATCCACCTCATAGCGTGTCAATTGCTCGGTTATAATCAAAAAATCCTCATCGAGCGTAAACCGTTGATCAACGATTACCTCAAGAGGATTGATTTTCGACACCTTTCCGAACAACACAGCAACGGGATTTCCTGCGCTTATCGCATCTATTCCTAGTTGTCTTATTTTATCTGCAATGCTCATCATATCACCTTCAAATCTAATGTCATGGTGTACTCTTCACCACTGAAATTATGCGAACATTCATCAATCAGATAAGGACTATGAATTGCTAAGTGGGCAATTTGCATATGGACATAGCAGCCGGCACGCACGCTTGTCTCTCCAAGGGCTTCGATTCTTAATTTTTTCGTTGGTCTGTTTTTCAATCGTGCCAGAGTGTCAAGCAGATTTCTGATTTGCGCATCGTTTTGGTTCTCGCCAACTTTCTGGTAGAGCTGCAGCCTACCCCATTTTGCAATATTCTCGCTGTCCTGAGCAATATGCACATCGCGTCCGCCTGTTTCTTTGTTATCCCTGACTAATTTGATCCGGTTGTACGTATCCTGATCAATCGATCTTTCGAAAGAATGATCGATCATAAGGCTATCGTCGCCAATCATCAAATCTAGCATCATATCCCTCGCATCACGCAAGGCAAGCGCACCGAACTCATCGTAAAAATTGTAAATATTCCCTGTGTTGATCACGGTCTGATCCAATGCCTTGCAGATGATATCCATAAGCTTCTGACCATCTTCATGAACGGTCGGAATAATATACTTGGTGTCAACAATCATCCCCGATTTCAAACCGAAGTCATTCGCGATTCGCTTAAGCAGAGCAGCAGCCGTTATATTCTTCAATACATACGTGTCGCTTGCCATAAGGTATCTGATTTGGTCATAACACTTTACGGCGATTTGCTCATCTTGCCCACTTCCGATCGTGAACACATATCCATAAAAAAGAGGACGTCCATCCCATTTCGCTCGAACGATGTCCCCGTGATTCATCCTGAAGTTCCCGTCGTTAAGGACTGAAAAGTCAAAACTACCTGGCTTGCCAATTCTCGACGTCTTCCATGTTGCATCATATACTAGTTCAGATAAGTCCCACACGTTACCATCTTTATTATCTAGTAATACTTCTAGCATCGTCCCCCTCCTATCATGACAGCTTGATGACCTTGCCGACAGGCAGACGCTTTAGTTCTGCATCCGTAATCCCGTTTAACTTTTGTAGAGATCGCCATTTCGAATCATCGCCGAGAATTTTCTTGGCTACTTTCCATAGATTATCGCCCGGTTGTAACGTATATGTCGTTGGTAGGATACGGGTATCCGGACGCGTCGGCCGGGATTGATGCTCGTTCATGATAACCTTCTTACTGCCGGAATCCGTTGCCAACGTTTGAATATTGACCTTCTTAGCCTCATAAGGACGATATTCCTTAAAAGAGATTTGATATTTAATGTCTCCGACAGCCCCAGCTTCTTCGGAATAAGTGAATTTCTCAATGCTTACGTACATGCTTACTCCTAAATTTGACCCTATTAGGTTCAACATGACAGGCTGCTTTTTTGTGCGCCATGAATTAATTTTCTTAATATAATGGGCTGGCCCAAAACATTCGCGGGCACTAACATTCGCCCCTGGGTACCACCGATTCGGGAAGAAACTTTCAAACGAAATTTCAGCCAACTTCGTCTTTCTAATGACATTAATTTCCCCGACGATGGATATTTCATAGGTCTTGTTGTTACCGCTCTCCGTCACTTCGAGGACTTCAGGTAGCACAGGAAAAGCTAATGCTTCCGTTTGATTATTGAAAGATAACGTCAATGAATAACTCATTTGTACACCCCCGCCGCCGTGGCCGCAATCTCTTCTTCCAACGTTCGTTCAATTCTCGCAATGATCGAATCAATATCCGTTGGTTTATTGACTGGGCCTGTGGTGACTTGCACCGTTGGGGTTAAAGATACGAAGTTTTGGATGGATTTCATTTCAGCAAGCTCGCGCATCGTCTTCAAGTCTTCGCTTGAAACATCTACCGTGTCTTGAATCTTCCCAACTTCGCCAACTCGATCGATATTTCTCATCGAAGATAGTTCTGAACCCGGATTACTGGATCCTGTTATCTTTTTTTCTCCATTTGTTATCGTTGATAACTTCTTCATGAAGCTATCCGCCCCGTTGTAGCCCTTCGCATACCCCGATTTATAAAAGTCGTTAAGATTTTTCTGCTCCATTCTGTCAAACTTTACGACGTTTTTATCGCTGACGGGTTCTTGAATTTGTGACATCAAGTTTTTTAATCCATCACTTAAGATATGCGTATTATTCGTATCGATCATTGCCGCTGTTTTGAATTCCGTACCGAATAGATCATTCGCTTTTTTTACGAACCAATTGAATCCTTCAAGAGCTTTATTTACAGCCGAGAGAATAATCTTTACAAATCCGCCACCAAAATCCTCCGCAGACCGTATCATATTGACTAAATAATCGCCAAATGTCATCGTGAGATCATAAAAAAGTTTTTTTACTGCATAGACCGGGTCAATAAATAAGTTGATCAGAAACTCTGCAAAACTAACGAGCGTATTCCAGATCAACGCGATCAAATTGTATACATTGGCATATAAAGCAAAGAAAAAGCCGACCACTGCACCCACGACTTGCTGTGCGGAGACGCCGAAATAAAGCAAAGCCGCTACGATCGCCGTGATCAATCCGATAATGATGAGCATTGGCGCATTTAGCGTAGCCCATACGGCTAAATTCGTAAGAAGAGCCGCTGTCATACTCCAAATTCGTTGAACCATCATCGTGAGCCAATAAGAAGCCACCGCCATTAAAAACCCGATCACGATCGGCTGATTATCTCGGATTATGTTCATCAGCCACATGACGCCATCTAATAAAGGCGACGCAGCACTTGCCGCGATCATCATGCCATCTGTTAGACCATTGAAGAAGTCATCCACCGCCTTGCTATCAAGGAGACTCACTAAGGTATCAAAAAATGGCCCCAATGCATTTACGACTTTTTGTCCAACCGAAGCGAATTTGAACTTGAATGTTTCGATGATCCGATTCCATTTCGCAGCCGGCGTATCCAGCATCTTTTCAAATGCTTTTTGAGTCATATTCTGCTGGTTCAACAGTTGATCCATCCCTTTAATAAAACCATCAATGTCCCCGGAAGCTCCTGCTTTTCTCGCATCACTATCCTTAAGCACAGACTGCGGAATATTGAACTGTTTCGATACGGCTGCATAGTCGCCCGACATGAAATCCTTGAGTGAGCGGGCTGCCCCTTCAAGTCCCTCTGCTGGATTTAGCTTGGCAAGCCGCATAGCTAACAAGTTGAGTTGCGTTAGCTTCTTCGGATCTGTGGTGGAAGACATGAAAGCATGAGTCCCATTGAGCGTCGCGTTAACATCTTGACCATATTTCAGAGCACTCTTAGTCACTTGATCGAATATCTCTTCTCCCCGAGCCTCATTTCCCGTTCTGGCAGCAAAAGTATCGATCATGCTTTGCTGGGACATGCCGGGTTTAATCATCATGGTGTTCATCGCATTTGTAATCCTTTTTATTGGCCCTGCCATCTTATCAAACATTTTTATTGTATCGGAAACCGTTGCCATCGCTTACCTCCTTTCGAACAAAACTAAGCGCCCTGATCTCAGGACGCTTGCCTTACGATTTAGCAGCCTTTTCTGCCTTCAGTCTGATTTGGATCATGGCAATCAATGCTGCTCTTTTGCGCGGCTCGAGTTCAACGAAGTCCCAAGGCATGATACGTAATTTATGGAGGGCATAGTAAGCGTAATTCCCCTCACCATCGCCCCCCTCGATTAGTTTTTTACCTCTTCAACCAGGTCGTTGATATCTTGATCGAAGCCGTTTACCGATTGAACCGCTTGAAGCAATTGACCATATTCGCCGGCTAGAAGCATTTTGCGAAGCAGGTCATCGGCGCCGATGACGCCATATGACTTTTGCAAGTCAGCCTCCTTCAAGTCAGGGAAGACGACACTAGCTACGATCATTTTCGTCATGTAAGACTCATAATCAATTTCAGGTGTCGTCACGCCGCCTTTACCTTTCACCTTCTTCGTAGCTGCTTTACGCAACTCCGAGTTTTCCCCCTCAGAAAGTCCACGTATTTTCCAAAAAATAGGCTTCCCGTTATCGCCTTTAAACCGATCCGAGACAATGACCTCTTGCGTGACTTCAGAAACCACGTTATTGGCGAAAAAAGCGCTTAATGTACTCATATTGATTTATCCTCCCTAGATCCCTTGGATCGAATTGAATTGGTCCAGAATATCGTAACCCTCGAATGTGAAAGGAATTTCTTCTTCGAGCATATCGTCACTTGACGCATCGAATTTAGCTGCAATAATGCTGTCAATATTGCAATTCTTAAGCAGCGTTGTTTGCTTGCCTGTGGCGCTTCCTGGTTGCTCATTCACCACTTGAAGGTCGAACCAGAAGTCTGATCCCGTTTGAATGTAATCTCGCATCAACTGGCGGAATGCAGTTGAGATATAATAAATCGTAAGAGTGCCACTCCCTTTCCACCCTGCAGAACGCTGAGGTGTATTGGTTCTTCCCAACATCGGAACATCCACTTTATTTTTTTCAATCGTCGCTTCTAAGCTTTTTGCATAGAATAATTCTTCAACACGTCCGTTAATCGTTACGAACGCCTTTGCTTGCTTCCCACTAATTGCATCCTTCACGTTAAAAATTGCCATCTTTATTCCTCCTTACTTGACCGTTACTGTCATATAGATTTTTTCAATGCTATCAACGGGTTGAATCGCCAAATTAACGACAACGGCGTCTGAATCGTTACCCTGCACTATGACAATGTCCGTTTGTGAGTTGAAATTTTGCACGGCCCCTAGCCCTTGAAGCGTCGTCATGTAATTGATAATCTCGGCTTTGAACAAGTTCCGCCCTTCAGCGTTATTGCTCACTTTACCGATATAGCTCGTACTGAAAATACGCTGCAAATCATTCGCGATCGAGTCAAGCACTCTTACGATTCGGTTCTTCCGGAATTGCTTTCCTTTATCCGACGTGAATGTTTTCAGCGAGTTAACGTCCTGCTCGATACGCACTTCTCCGTTAACAACCGATAGCACCAACTCACCGTTTTTAAGTGCCTGGCCGATTTCCGTGCTTGTATATTTAGGGAATACGTCCACCGCATCAGGAATGACCGTATAAGTCAATGAATCGTCAACGTTCGCGGCAGCTTCCATCGCGGCAATTTCCCAGAGCATATGCAACGGATCTACCTTCATCCCATCGGATGCAATAATGCTATTCTTAAGGTTGATTACCCCCTCATGATCTGCACCAGGATGATTGTATAGCACGGTCTGCATCTTCTTCCCTTCACTATCTCGCAGACGCTTCGTATAAGCCACTGCCAATTGTTTGATTGAACTGTCATCCGTAGGTACGGTCAAGACATTGAAATCTTCAACCTCGAACGCTGTGAATGCTTCAGCATACTCGCCGTTACCGCCTGTTCCTGCCGTTCCGCCGGTTAAAGAAACCCCGGCGTTAGCCGTCAATGCGCCAGTACCAGAGAAAACAACGAAATCGTTCGATATAAGTTTATCGGCAGTCGCGACCATCTGCGAATCTACCTCTTCACTTTCAAGTAAGGTTTTCACGTCAAAGGATCCCGCTACATCGACATTTGCTTCGATAATAATCTTCAAATCATTCCCGCGTACTCCCTCATACTTTGCTGTGGCTGTTAAAGTGCCAGCCGTAGCCTTCGCTTTTACTCCACCTTTAGCAGATAGTCGATACAGCAGGATTTTGCTCGCATGTCCCATTGCTGCCGTAATATGACGTACGCGGTCATCGGTCGCGCGATATCCAATCAACGCTAATGCCTTGTCCAAATACGTCTCAGCATTTAGCACGATAAGACCGTTCGGATTACCCCAAGATAATGCGGCTGGTACCGCTAAGATTCCTCGTTCACCCATTGAACCAACTGATGCTTCCTTTGATTTAAAATTGATATACAACCCTGGTCTATCTTTGCTTTGACTCACCCATGTTCCACCCATTTATTTCGCTCCTTCGTTCATAAAATTTTGAATAGCAACCGTTACTTGTTCTTCTGTAAACTTACCGTCTGCATCAAGCACGACAGACATAATATCCTTCTCCACGCCTGTAAAGCGGATCGAAGATAGAAATTGATCCTTGGTGTACGAAATTTCCTTCGATTCTTTAACTGCCATGTTTAATTACTCCCTCCTCCGTTAGCGTCCGCATTTTCGGTTCGTCCGCTTCGACTAACCATATCCGAATCTCGAGATCGAAAAAGAAATGCAAGACTTGATCTGCGACATTATGATGCATATGGATCCCGTTATAGGCAGAGCCGTCAATCGTAAAGCTATCTAATGTGCTATAAAGCCGCTCTGCCATTTCATGGGCATCTGCATTCGTCCCTGATTGCGCGATATGCTGAACTTCAAATCGATAGATTCGATGATACCGGCGTTTTAGTTCTTGATCTTGTCTGCATGATAGAAGATGCACCAAAAAATATGGAGCGCTAACTCCCTGCCCAATCTCTTCACCAGAAACGGTCACCCCATCGAAATGATCATGCAAAGTTGAAATGACCCCTTTACGTATGCTATTAATCGTTACCTCCGACATGTAATCACCCCCTTTCGTATGATTGAACACTGTGTTGACCGCCGTTGAACGCACAATAAAAGCACTCTCCATGACGGAAAGTGCCTCTTCTACTTCATTGGGTATCAAATTGTATCAATCAAATGAATCGTTTTCTCATTTGCTCTACAATACAATCTTAACACCCCAAAAACCTAATAACACATCCGTAAGCAGGAAAAATCACGACCTTTTCTGGCCCTTAAAGATAAAAAAAAGAGAATCACCATTTCGTGATTCTCTCTCAGATCGTTAGTATTGCAAAATATTTAATGCGCTGGCTATCCGTTGAACTGCATTCCATCGCCATTTTCTGTACGTCTTCTCGCTAATCGGCGGATCAAATACAAAGTTGTAAACCTGATAATCCTTCATATATTCCTTCATGTATCGATTTTCGATAATGAGACGTTCCACGGGATGCAGTTTACTTACAATGGCTTCAATTCTTTTACAATGCATGAGTCTATCCTTAATCTCAGCATTCTTTATACCTGCACGAGCTGTCGAATCGTTAATCATCCCAGTTGAACCGCTATGTAGACGATATTCATAGGATTGTGTTACTGTAGGCTCGTCCGTATTTATCTCACAAAACTTATTTAGACGGTACAGTTCAAATTCTCTTTCCACCACTCGATATGTTGCCTCTTTATCTACTGCTTGAACGGAAATCATTCAATCACCTCATCGATTTTTTATATTTCAGAACATTACAAGTGCTTGCGATTCAAATGCCATAGCGAAGCTCTGCTTACATATAAATCATCCATCTCCTTTCATCAAGTAGCATTTCGACCATATTTTTGATTTGTTGCTTAATAGGTTCACTTCCTTCTTGAGATAAATATATAACTCTATTGAGTTATATACAACATCTCTTGCAACTCAAAAGTGTTCTAATTTCCGTTATTTCCTACATATTCCTTCATCAATCTTGACTTATCGCACTTTTTAGTTATAGAATAACTTTATTGAGTTATAACTACTTAGTTATAGTGGAGGTATTGGAAGTGGAGATCGCTGAAATGATACAAAGGTTAATGGACGAAAAGGGAATATCGATATACAAATTGTCCAAAGAGACCGGTGTTTCCTATACCGGACTCACGAAGATATTGAATGGCCAGACAAAACATCCTCAAATCGATTCGCTAAAATTGATCGCTGATTATTTCCATAAACCTGTGGATTATTTTACAAGCACTAGATCACCTGACGTAAGCCCTCTCCCAGAATGGGCAACCTCGAAAGACAAGATGGATTTCAAAAAAATGCTTGAGGAAGACGCTCCTGTGATGTTCGATGGGGTTCCGATTGAAGGTCAGGCACGACAAAGGGTACTAGACGTACTTACAGGTCTTTTCTGGGAAGCAAAAGAAATGAACAAGAAAACGTACGGCCAGAAAAATTCTAAAAAAGAAAGTTCTAATGAAGACAATGAGTAGGTGACAATTATTGGATAAGACTATCCAGAAGCTGGTGCGAAAATTTAAGACGAATGATCCATTTATCATTGCATCAGGATTAAACATCATTGTTAAATATGCAGATCTCGGAGAAGGTACACGGGGTCTTTATTATAAAAAACTGAGAAGAAGATTTATCGTATTACAGGAAGGGATGGATGATCACTGGCAACGACTCGTACTAGCGCATGAAATTGGCCATGATCGACTACATCCAGGAATCAGTAGATTTTGGCTCGATGAACAATCTTTCTTTAATGCGGGGAAATACGAGAGGCAGGCTAATGAATTTGCAGTAAAATTATTAATTCATACGTCTAGTATCGAGCAAGATGAGTCCGTTTTTCATTTTTTACTCAGATGCGGAATACCGTGCGAAATGCATCAATATTATTATGAATAA

Protein sequences of DBSCAN-SWA_1

>NZ_CP045293|2699370:2735515|2735101_2735515_+|WP_152393766.1|DBSCAN-SWA
MDKTIQKLVRKFKTNDPFIIASGLNIIVKYADLGEGTRGLYYKKLRRRFIVLQEGMDDHWQRLVLAHEIGHDRLHPGISRFWLDEQSFFNAGKYERQANEFAVKLLIHTSSIEQDESVFHFLLRCGIPCEMHQYYYE
>NZ_CP045293|2699370:2735515|2733187_2733625_-|WP_152393763.1|DBSCAN-SWA
MSEVTINSIRKGVISTLHDHFDGVTVSGEEIGQGVSAPYFLVHLLSCRQDQELKRRYHRIYRFEVQHIAQSGTNADAHEMAERLYSTLDSFTIDGSAYNGIHMHHNVADQVLHFFFDLEIRIWLVEADEPKMRTLTEEGVIKHGS
>NZ_CP045293|2699370:2735515|2715934_2716297_-|WP_152393745.1|DBSCAN-SWA
MLKYSSYQSVYNNQSKVVNRGSFLKKKVVQVVLFLVLVCSLTSMGLLNAFAADTRDGERNANIPLQIVVSPGDTLWAIAKEHKPDGMDVRNYIEEIKELNGKRNSSIQSGEVIKLPVLKG
>NZ_CP045293|2699370:2735515|2727108_2728062_-|WP_152393757.1|DBSCAN-SWA
MLEVLLDNKDGNVWDLSELVYDATWKTSRIGKPGSFDFSVLNDGNFRMNHGDIVRAKWDGRPLFYGYVFTIGSGQDEQIAVKCYDQIRYLMASDTYVLKNITAAALLKRIANDFGLKSGMIVDTKYIIPTVHEDGQKLMDIICKALDQTVINTGNIYNFYDEFGALALRDARDMMLDLMIGDDSLMIDHSFERSIDQDTYNRIKLVRDNKETGGRDVHIAQDSENIAKWGRLQLYQKVGENQNDAQIRNLLDTLARLKNRPTKKLRIEALGETSVRAGCYVHMQIAHLAIHSPYLIDECSHNFSGEEYTMTLDLKVI
>NZ_CP045293|2699370:2735515|2728758_2730564_-|WP_152393759.1|DBSCAN-SWA
MATVSDTIKMFDKMAGPIKRITNAMNTMMIKPGMSQQSMIDTFAARTGNEARGEEIFDQVTKSALKYGQDVNATLNGTHAFMSSTTDPKKLTQLNLLAMRLAKLNPAEGLEGAARSLKDFMSGDYAAVSKQFNIPQSVLKDSDARKAGASGDIDGFIKGMDQLLNQQNMTQKAFEKMLDTPAAKWNRIIETFKFKFASVGQKVVNALGPFFDTLVSLLDSKAVDDFFNGLTDGMMIAASAASPLLDGVMWLMNIIRDNQPIVIGFLMAVASYWLTMMVQRIWSMTAALLTNLAVWATLNAPMLIIIGLITAIVAALLYFGVSAQQVVGAVVGFFFALYANVYNLIALIWNTLVSFAEFLINLFIDPVYAVKKLFYDLTMTFGDYLVNMIRSAEDFGGGFVKIILSAVNKALEGFNWFVKKANDLFGTEFKTAAMIDTNNTHILSDGLKNLMSQIQEPVSDKNVVKFDRMEQKNLNDFYKSGYAKGYNGADSFMKKLSTITNGEKKITGSSNPGSELSSMRNIDRVGEVGKIQDTVDVSSEDLKTMRELAEMKSIQNFVSLTPTVQVTTGPVNKPTDIDSIIARIERTLEEEIAATAAGVYK
>NZ_CP045293|2699370:2735515|2700358_2701879_-|WP_152393729.1|DBSCAN-SWA
MKWESRLSIHQVLGGRYRVMKQIGEGGMSYVYLVEDLKLVGKRWAVKETRLQQPGNAAGVAAEAAMLIRLNHPNLPQIVDFLGPDAEGYIYLFMDYIEGETLAVDFERRGRSLAFDHILRLGIQLCEVLQYLHQCQPPIVYRDLKPTNVMMDVHGQIRLIDFGIARHFKPNQEDDTVCLGTVGFAAPEQYTGKQSDTRSDLYGLGALLMHLITGGRTSQFGQAGMDAMPQEVPLAFRQLLKHLLDRDPNLRIQTAQEVREKLEQIHMEMAKTWRGNQPVSTTHRWRGTGTIALLGIDSGVGTTHTAIMFAHYLAASNQRVACVECMRTEAFYRIRSIFDGEPIRRSGEHFTIHGVDYYPYLESRSLIPLLHTDYDVIVLDLGVYGDNAAMFAEFLRANISCVVASGAEWRQEDLSDFMRRAGFAHQAASFIGLIPLATQQTIRDMEQNFIVPQLYAIPYHVDPFHIDDMARKALSAILPMEQTHSNWRTGLGKLLFSRRSRRDVKN
>NZ_CP045293|2699370:2735515|2724916_2725330_-|WP_152393754.1|DBSCAN-SWA
MSYPDQVDKFTEKLNKKLDGSVYVIEEILVIAGGSFEGLLAHDNITNNSIRVYTGPKLTGKEITDYVISVPADTPWRRSIKIYTEVSKVYVTYETNGDIVEADDINQLQSSIISIQAELERYKEVGIIDGGYFARGK
>NZ_CP045293|2699370:2735515|2706370_2707456_-|WP_152393736.1|DBSCAN-SWA
MKPIHFAFTGLGAIAKTHIVALRAMPVIQKSPFVPVLDTLVTRNPDGNREQALAMGFQQVTNSLDEALTNPTVHIVDICTPNAMHFTEGTAAASADKAIYFEKPLTEAYSRTEELMNHIPANTLQQVALVYRYHPAVMKMKAILQEGIIGDVLQCNCSYLRSGYLNAERPVSWRLDDTISGGGAVTDLGIHVIDLIAHLFGELTDVHGETNIFVKERPKAQGSDERVQMTVDDWASFFYTTKSGVRGTGEVSRIAWGSDRFSVQIVGTRGSITCDLEKDITPKVSMLSGATPALPVPSSLQLIPNDKTTMGVFVDSHFGALNHFLHRYIGEDAWANEGLAPTMKDAAHAEMWIDRILRSKV
>NZ_CP045293|2699370:2735515|2726360_2726660_-|WP_152397218.1|DBSCAN-SWA
MTEGIDAVKQSVYKILNAERFVHLIYGNWYGFQGNHLIGQSEAVLRVELERRIREALMQDDRISDITDVQIIVQGDEALVDFTVVSTYGDFRMELIRDV
>NZ_CP045293|2699370:2735515|2734656_2735091_+|WP_152393765.1|DBSCAN-SWA
MEIAEMIQRLMDEKGISIYKLSKETGVSYTGLTKILNGQTKHPQIDSLKLIADYFHKPVDYFTSTRSPDVSPLPEWATSKDKMDFKKMLEEDAPVMFDGVPIEGQARQRVLDVLTGLFWEAKEMNKKTYGQKNSKKESSNEDNE
>NZ_CP045293|2699370:2735515|2720848_2721196_-|WP_152393751.1|DBSCAN-SWA
MNVKYYRLTDNFKIEIGASITYTYGGVPIDQLLGGFPRMENGKEVAYICIDEKVTQAPKEHVEEVTAEIFSEAAKRDFVSDPTEIDKLKAENESLKTKQNLMQSALDVLILGGTL
>NZ_CP045293|2699370:2735515|2730774_2731197_-|WP_152393760.1|portal|DBSCAN-SWA
MSTLSAFFANNVVSEVTQEVIVSDRFKGDNGKPIFWKIRGLSEGENSELRKAATKKVKGKGGVTTPEIDYESYMTKMIVASVVFPDLKEADLQKSYGVIGADDLLRKMLLAGEYGQLLQAVQSVNGFDQDINDLVEEVKN
>NZ_CP045293|2699370:2735515|2717244_2718006_-|WP_152393747.1|DBSCAN-SWA
MSLFIALDDGHGMQPPGKRTPLFKDGTRSKETGEPFMHENEFNRAVVALLDEHLQRCGFRTLLVAPGDSDVPLKTRTDTANQSGVDLYVSVHANAAGETWGSVNGIESFYYPGRVTSMKAAEAIHARLVQGTKLRDRGVKPANLHVLRESTMPAVLVECGFMDNMEEAKLLLSDAYRDLCAEEIARGVCQYFGIAYVETEANVMLAKEDANKLIDLYLKPAWEIAQQKGDEAGKKEANRLANELRKASGQAPQ
>NZ_CP045293|2699370:2735515|2721207_2722947_-|WP_152393752.1|DBSCAN-SWA
MKTTANLGLKKPEGTDIVNIDDLNGNMDTLDAEVVKKASSTADGRMTKEDKGKLDGIEAGANKYVHPATHPASILVQDANNRLVTDAEKTSWNAKETTTGAQTKVDNHANKTTAAHDASAIAVNDTDFTEKTVLAVLKSLKSLANNLKSKVAGAIGAPLSATDDASQMESKINTIKSTAATNLTAKGVAASASETLTALVNKISQIIRGSGNATTADVLATKTFTNDVGVQLTGTMPDYSAYPNNGGYVFALSTKGDSMTSLIMEPPTGYYKQGKNVNGYGALIASDTNYIPANIIKGKSIFGVVGTAEQSQITNELLKVVGTPRGLTALTSRMVNAPLGFDVNKGLFGFYDSSNSTAKVWQIGGDGNSYEFFSIPAGQYDNGAIQQLRGAKGHAYDTTWYCGSIAGNYLRKVQISYAAGDNRWNYTELGTVPNVKGYQIGNDDCQFYNDKFYTIIGGATSYTLSIYNTAGVLLNNYSGSYEYEIGGGSGTMTYAMCEGKFMISNQNTPLQTMIITANGVIQYHYKVTTNFYDRMFNRSDPPSMIKGLDGKKYLCMNAPSTVLFQPQSYGQYIYTGNLY
>NZ_CP045293|2699370:2735515|2703124_2703910_-|WP_152393731.1|DBSCAN-SWA
MISMQHIKLRREERQILNDITLQMNEGEHWVILGRNGSGKTTLLEMMTGYMFPSSGQIDVMGNRYGQCDIREVRKKIGYISQSLMEKLTLRDPVWEVVATGEYGFLRFYQDIPEEVVAKARGLIDEMKLGHVADNPLGTLSQGERKKIMLARALMADPQVLILDEPCAGLDLYEREKFLDQINLLKKRNIALVYVTHHLEEIVPLFTHVALIHQGKLVAAGTKESVLTPEILIQAYEVPLSLEWVDGRPWIRVQGLEVNNR
>NZ_CP045293|2699370:2735515|2703906_2704233_-|WP_152393732.1|DBSCAN-SWA
MKEINEQDLLDRIDHVDVYRPFGLYLYTPLCGTCKAGMRMLHVVEAMLPDVELLQINLNFSPRLVARYHVRSVPGLFLFDPKRRGEPVQVYEMRSVEHLFNIIKDVIR
>NZ_CP045293|2699370:2735515|2728075_2728762_-|WP_152393758.1|DBSCAN-SWA
MSYSLTLSFNNQTEALAFPVLPEVLEVTESGNNKTYEISIVGEINVIRKTKLAEISFESFFPNRWYPGANVSARECFGPAHYIKKINSWRTKKQPVMLNLIGSNLGVSMYVSIEKFTYSEEAGAVGDIKYQISFKEYRPYEAKKVNIQTLATDSGSKKVIMNEHQSRPTRPDTRILPTTYTLQPGDNLWKVAKKILGDDSKWRSLQKLNGITDAELKRLPVGKVIKLS
>NZ_CP045293|2699370:2735515|2713005_2713449_-|WP_152393740.1|DBSCAN-SWA
MQIMQRKKMSMLAIACILLIALLAGCSGSNEGMNHDGMNMDMDMSEDAMNPIKVEIILPAQITANKDVVLQAKVTQTDKPVDDAKEVMFELWRGEEQEHEKIEAKLTSNGVYQIEKQFAESGEYTMIAHVTAREMHSMPKKTFEVAK
>NZ_CP045293|2699370:2735515|2708798_2712236_-|WP_152393738.1|DBSCAN-SWA
MNKLSIQEQMKHKILILDGAMGTMIQREDLTADDFGSEELDGCNEILVLTRPDVIQKIHEEYLEAGADILETNTFGATSVVLAEYDLQDRARELNLAAAKLAVDAANKYSTPEWPRYVAGALGPTTKTLSVTGGVTFDELVDSYYEQTVALIEAGVDTILLETSQDTLNVKAGSIGIRRAFETTGKTLPLMISGTIEPMGTTLAGQNIESLYISLEHLKPISVGLNCATGPEFMRDHIRSLSEIADTAISCYPNAGLPDENGHYHESPDSLAKKMAGFAEQGWLNIAGGCCGTTPDHIRALADTMSQFQPRSAFGTHPPAVSGIETVYIESENRPYMVGERTNVLGSRKFKRLIAEGKYEEASEIARAQVKSGAHVIDVCVQDPDREEAEDMKKFLELVVKKVKVPLVIDTTDAKVIDLALKYSQGKAIINSINLEDGEEKFEHVVPLIHKYGAAAVVGTIDERGQAITRVDKLEVAKRSRELLVNKYGMQPEDIIFDPLVFPVGTGDEQYIGSAKETIEGIRLIKEAMPECQTILGISNISFGLPEAGREVLNSVFLYECTKAGLDYAIVNTEKLERYASIPEHERRLSEELLYDTNDATLSAFVAAFRDMKVVKKEKASNLTLEERLGSYVVEGTKEGLIPDLDEALKKYTALEVINGPLMEGMSEVGRLFNNNELIVAEVLQSAEVMKASVAHLEQFMEKNESSVKGKIMLATVKGDVHDIGKNLVEIILSNNGYEIVNLGIKVPPEQIIEAYRKEKPDAIGLSGLLVKSAQQMVLTAQDLRNANIDVPIMVGGAALTRKFTKTRILPEYNGLVLYAKDAMDGLDLANKIMDPTHRQLMIAETAAIKESVGEEEEKKPLPKLTRAVRSNISQDAPVFIPPDLDRHILRDYPLGHIIPYVNMQMLLGHHLGLRGSVEQMLAEKNPKAVELKATVDEILQNAITDGTIRAQGMYRFFPAQSSGDSIIIYDPQDTTKVLHTFTFPRQQVEPFLCLADYLKSVDSGIMDYVGFLVVTAGNGVRELATKYKEVGDYLKSHAIQATALEVAEGLAERVHHMMRDIWGYPDPQEMTMKQRHGARYQGIRVSFGYPACPDLEDQGPLFELMKPEDIGIQLTEGFMMEPEASVSAMVFAHPQAQYFNVEKV
>NZ_CP045293|2699370:2735515|2718267_2718744_+|WP_152393748.1|DBSCAN-SWA
MNKQFIKTTATLFIGMMLGTVTIAAAAPEVFQASIAKLKIVVNGKEQKLKNSPLLVNGTTYLPVRDVAGLLGANVDFNKGTITIAQKKVQPTVNTIESINGRDLVEILGKKYPDFKISLSNEGLLKLGDNIIHLTVNDDSTLNVTPLKDSGFISKSDL
>NZ_CP045293|2699370:2735515|2712392_2712935_+|WP_152393739.1|DBSCAN-SWA
MAEIYIRNTKERISGEEDVRAFLANQEVLYEHWDPTKLPENLRERFVLSDEEKAEVLATYDVEIRDLAARRGYQIWDIITLSDATPNLEELLTKFEDVHTHTEDEIRAITAGKGIFIIKGKDDVGYFNVELEAGDVISVPEHTPHFFTLMDNRQIVAVRLFIEKDGWIATSYDDPAFQKA
>NZ_CP045293|2699370:2735515|2719808_2720000_-|WP_152393749.1|DBSCAN-SWA
MKGKYGFLHCYAHLSMITVKVGQRVGKGEMIGHQGSTGVSTGPHLHYEIRKKVRHHTVGLRRS
>NZ_CP045293|2699370:2735515|2704216_2704567_-|WP_152393733.1|DBSCAN-SWA
MIHVFLDDIRRCPEGFVYARSAEECLLLLEEADVNILSLDHDLGINQPNGTQLVKQMVLRGLYPREIYLHTSSLSGRKTMYELFYQNKPDHVILHNGPMPQSVLTRIREAAHERNQ
>NZ_CP045293|2699370:2735515|2716478_2717105_+|WP_152393746.1|DBSCAN-SWA
MSKISNRQQAILEFIRNEVRSKGYPPSVREIGEAVGLASSSTVHGHLDRLEKKGLIRRDPTKPRAIELLSQEESEHTHLYTQMIAKVPIVGKVTAGAPITATENIEDYFPLPEQFVHDQNVFMLSVMGESMIEAGIHNGDFVIVRQQQTANNGDIVVAMTEDDEATVKTFYKEKDHIRLQPENATMEPIRLNHVTILGKVIGLFRNMH
>NZ_CP045293|2699370:2735515|2731212_2731680_-|WP_152393761.1|portal|DBSCAN-SWA
MAIFNVKDAISGKQAKAFVTINGRVEELFYAKSLEATIEKNKVDVPMLGRTNTPQRSAGWKGSGTLTIYYISTAFRQLMRDYIQTGSDFWFDLQVVNEQPGSATGKQTTLLKNCNIDSIIAAKFDASSDDMLEEEIPFTFEGYDILDQFNSIQGI
>NZ_CP045293|2699370:2735515|2699370_2700516_-|WP_152393728.1|protease|DBSCAN-SWA
MPFRIMWIHSTLTIWHERPSRLFCRWNRRIRIGGQDSVSFYSQEGAEGMSKIRQRTKNLWIAGLSGAAIMGCLFLSYAVYSQLHVQKIKRDTEKQYEQQIAELQTARQEQQAKMGNVWVLKGNVAAGTRISAQQVEMQEMELRLLPANVVGTKEKIVGKISKIDLSANTVLIPSMFYEGQATPNDLRNEQFAQIQLPLNLRDQDVIDVRIQFPTGQDYIVLSKKRVKRVAGNTISLQLTEQEILMMSSAMVDALIHHGSIYGLTYVDPGMQSSAIVNYPSNAEVLALIETNPNIVEEAKTALAKVARKKLETALAEQQMRYSNLTLGPSTTPQSVVQNEVQSTTSETSPIDNRDDGVLTKEEQTKLFEQAPIPNDDAGSDQ
>NZ_CP045293|2699370:2735515|2702063_2703128_-|WP_152393730.1|DBSCAN-SWA
MNEQLEHQEQQHEITSKWICTANHGFIAYAQEELRRRFGQVKAMVLIPSEVILVTLPVDESQVIRELQTDPLIFLRHIQPVQQEFLLAEAGQEERNAAILSFVQSNQALHRGQSVAVQLRKASNDAGAVDLALLKSALEAGLSESGMETVTRDSHWIVSIFAGKDTVYVGISTPEDNLSDWSGGALRFQREEGQISRAKFKLLEAERAFGLDLASFSEGLDIGAAPGGWTSLLLERGLKVTAIDPAEMHPSLLENRRLTVLKKNASEVKFRESQFDLIVCDMSWSPMQMVRLVMDLLYALRSGGTAIVTVKLMHKKPLQTIRDISEKFSEHLEIRRMKQLVHNRDEITLYMVKY
>NZ_CP045293|2699370:2735515|2733895_2734321_-|WP_152393764.1|DBSCAN-SWA
MISVQAVDKEATYRVVEREFELYRLNKFCEINTDEPTVTQSYEYRLHSGSTGMINDSTARAGIKNAEIKDRLMHCKRIEAIVSKLHPVERLIIENRYMKEYMKDYQVYNFVFDPPISEKTYRKWRWNAVQRIASALNILQY
>NZ_CP045293|2699370:2735515|2705474_2706281_-|WP_152393735.1|DBSCAN-SWA
MGNSNKALLIDLDGTLYHGKHRIEGADLWIQELKSLQIPYLFVTNNSSRTPEDVAAHLAEMGIPATHADVYTSALAAAQYIQEHYPQGVRAAVIGEYGLETALREAGVEITEDQPEIVVQGIDRSFDYAKLTQAVQWIREGAAYILTNPDLLLPSDTGIMPGAGTLSAAIQAATREEPIVMGKPSKIIMNYALARLGCEPQDAIVIGDNPLTDLRAGQAAGCDTILVLTGLATEANKDQLLAQADVQPSWICKDLYEAAAVTSGRNAQ
>NZ_CP045293|2699370:2735515|2715625_2715826_-|WP_152393744.1|DBSCAN-SWA
MDFEKIVERINELARKHKSVGLTPEETVERDALRRQYIDGFKRSLKQQLDNIEIVDEDDNNPTIKH
>NZ_CP045293|2699370:2735515|2720254_2720623_-|WP_152393750.1|holin|DBSCAN-SWA
MALIVGTIGAPVFNFFYGGNKMASGLMIALVFFIVMDWITGVWAAKMDRTYASKYGIDGVVRTFFILLLPAAGHLLDEVFGFPDIIFGALAVGVLYHTLQSMTANAVWAGWADWLPQKVLDH
>NZ_CP045293|2699370:2735515|2723884_2724832_-|WP_152397217.1|DBSCAN-SWA
MGFCTDTKEVFIGDGAVNNFVGRAMSGTEAARPVAANLGRFYFVTSGTNSGYLYFDTGTAWQRVNAQKISELIGTIDDGADGTTYARVKKSEITNGQVNKVSDGINTKTAAEIKTHIDDVTKHRVINDSGGSSVDLWSAQKIKNEIELAKHNIEPQASVKNRTTAAPPASPIEADRYVIPSGASGVWAGKQNQIAEWQSGTWMYYPPAVGWTCYVDDEQKIYSWNGTSWVRTGGALQTITAGNGLTGGGQADSVTLTVGQGNGITVAAESVSVKAGKGVLVDGNGVAANIDGTSISYDAANGNKLMVSIVDGGTF
>NZ_CP045293|2699370:2735515|2704592_2705414_-|WP_152393734.1|DBSCAN-SWA
MLELPELETYKKLLSEQIINKRITGVQVKEDKLINSDTAAWSKQLQGREVLFIERRGKQLLFHLDNGKRLLLNLGAAGQIQLNGLEVDEGSHANAQVMISFGDQALRLLGIRQGYIHLLSAKEADQELSNLGPELLDRKMNLEKFQTLFARKRGMLKSALVNQSFIAGLGNGYADEIAFEAALLPSAKLQDLSEESIERLYHSTMTVLHDAIEYGGMGEERLNAKDDLTGGYKSHVRVIERDGQACERCGATIQKAEVGSRKTYYCASCQKEK
>NZ_CP045293|2699370:2735515|2731692_2733021_-|WP_152393762.1|tail|DBSCAN-SWA
MGGTWVSQSKDRPGLYINFKSKEASVGSMGERGILAVPAALSWGNPNGLIVLNAETYLDKALALIGYRATDDRVRHITAAMGHASKILLYRLSAKGGVKAKATAGTLTATAKYEGVRGNDLKIIIEANVDVAGSFDVKTLLESEEVDSQMVATADKLISNDFVVFSGTGALTANAGVSLTGGTAGTGGNGEYAEAFTAFEVEDFNVLTVPTDDSSIKQLAVAYTKRLRDSEGKKMQTVLYNHPGADHEGVINLKNSIIASDGMKVDPLHMLWEIAAMEAAANVDDSLTYTVIPDAVDVFPKYTSTEIGQALKNGELVLSVVNGEVRIEQDVNSLKTFTSDKGKQFRKNRIVRVLDSIANDLQRIFSTSYIGKVSNNAEGRNLFKAEIINYMTTLQGLGAVQNFNSQTDIVIVQGNDSDAVVVNLAIQPVDSIEKIYMTVTVK
>NZ_CP045293|2699370:2735515|2707795_2708731_-|WP_152393737.1|DBSCAN-SWA
MELYFLGTGAGMPTTERNVTSIALRMFDERGTFWLFDAGEATQHQILKSPLKPSKLEKIFVTHLHGDHIFGLPGLLSSRSHQGGTEKLEIYGPTGLRQYLKTSLQLSQSHLNYEIRIIEVDEGIVFEDEQCKVEAARLDHRIESFGYRVMEKDRPGRINVEALTKAGIPPGPIYGKLKKGEDVVLDDGTVITPDEFIQAPIPGMIITILGDTRPCAGSRYLAQNADVLVHEATFMEGLESLAENFYHSTTRQAAETARDAAVGQLVLTHFSARYSDIEPLVAEANVIFPHTIAANQLELIPIHRRSHTGQS
>NZ_CP045293|2699370:2735515|2725333_2726368_-|WP_152393755.1|plate|DBSCAN-SWA
MYEAQSFEVILNRMLNRVTNDVDKRPGSVIYDALAPAAAEMAQMYMDIDMFLRLTFASTSSGEYLALRAAEMGVSRNPATKAKRQGVFYSGNEYLDVPLGSRFSIDDVTYVARDRIDPGIYILECEVAGNVGNTPIGPLLPVDYVPKLTRAVLTDIVQEGVNEEPDEKLLAKYQLRVQQASTSGNAYQYKQWAITVQGVGDAKVFPLWNGPGSVKVVIADLDKKPADPASVAQTSDYIEEVRPIGANVTVVSGVGKAIIVKAKVALATSYTLQSVTEGFKSLLTDYLKSIAFEMTYVSYARIGTLLMSVPGVLDYSAMSLNGGTVNIPLADEEIPVFGSVELGV
>NZ_CP045293|2699370:2735515|2715058_2715577_-|WP_152393743.1|DBSCAN-SWA
MARSWERMVRKNTKNVNKVRKKQGQQMIGSSREAKSDVDRYVGRNLILPITLVAFGLLYAILYSAVDQKTSPALFWGTVGLYIFLGVVIFLRRPYISVGKSSIGTRRFNRDVRLDASQIKEITVQKGYVVISPKAKGSNWVFSRLMNRYETAVIGERLKEFARVNHVPFEER
>NZ_CP045293|2699370:2735515|2722951_2723566_-|WP_152393753.1|DBSCAN-SWA
MYGQYQYGSLQFGAEVEGKDPIDGYIPDLLKYLPQYWHEISEMACIQDVAAREIGSARFALSELGNQFFVQTATWGLAYWERELGLTTDNTKPYERRREMILAKLRGSGTTTKEMIKGVAAAFSGGETEVVEYPSEHRFEVQFIGVMGIPPNMAGLKQVLEEIKPAHLTYSFKYTYTWWETLKGLTWQQANTKSWGELRTYKGE
>NZ_CP045293|2699370:2735515|2726755_2727112_-|WP_152393756.1|DBSCAN-SWA
MMSIADKIRQLGIDAISAGNPVAVLFGKVSKINPLEVIVDQRFTLDEDFLIITEQLTRYEVDLELAYVNMSGNTQTETQQSMKNIVIIREGLKVGDVVILLRIQGGQKYVVWDKVVTT
>NZ_CP045293|2699370:2735515|2713475_2714039_-|WP_152393741.1|DBSCAN-SWA
MKKLMFLMLGVMLLLTACGGAKQTSSMKVGDFAYTDQAGQAFGLADLKGKVWLADFVFTNCTSVCQPMTFNLTDLQKRLKAENLDVTFVSFSVDPDRDKPEVMKAFADKFGVDFASWHFLTNYKLEDIQAFAKSSFKTIVEKEPSSDQMIHGTSFYLVSKEGYIMKKYDGVEDVPYDQIIKDVKDLI
>NZ_CP045293|2699370:2735515|2714224_2715022_-|WP_152393742.1|DBSCAN-SWA
MTIKAVLFDLDDTLLWDDRSVKESFEATCVAAAQAYPHIQPTALEEAVRREARALYETYPTFPFTQMIGINPFEGLWANFTHGEQQEFRQLQALAPGYRTEAWTKGLQALGVEDAALGERLGLLFATERRARPYVYEETFQILDELRGNVKLLLLTNGSPDLQQEKLNGVPNIIPYFDHIVISGAFGEGKPASSIFRHAMAALDIEPHEGLMVGDKLTTDIKGALGVGMHAVWVNRHGVQRSDEIVPDYEITHLSELHNIINQHA

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_152393728.1|2699370_2700516_-|protease	zinc metalloprotease ZmpB	NA	NA	NA	NA
WP_152393729.1|2700358_2701879_-	protein kinase	A0A0U2U263	Niemeyer_virus	2.3e-14	26.9
WP_152393730.1|2702063_2703128_-	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_152393731.1|2703124_2703910_-	ATP-binding cassette domain-containing protein	W8CYL7	Bacillus_phage	1.2e-11	30.2
WP_152393732.1|2703906_2704233_-	thioredoxin	NA	NA	NA	NA
WP_152393733.1|2704216_2704567_-	cell division protein FtsJ	NA	NA	NA	NA
WP_152393734.1|2704592_2705414_-	endonuclease VIII	NA	NA	NA	NA
WP_152393735.1|2705474_2706281_-	TIGR01457 family HAD-type hydrolase	NA	NA	NA	NA
WP_152393736.1|2706370_2707456_-	gfo/Idh/MocA family oxidoreductase	NA	NA	NA	NA
WP_152393737.1|2707795_2708731_-	ribonuclease Z	NA	NA	NA	NA
WP_152393738.1|2708798_2712236_-	methionine synthase	A0A140XBC7	Dickeya_phage	2.7e-10	50.0
WP_152393739.1|2712392_2712935_+	cupin domain-containing protein	NA	NA	NA	NA
WP_152393740.1|2713005_2713449_-	hypothetical protein	NA	NA	NA	NA
WP_152393741.1|2713475_2714039_-	redoxin family protein	NA	NA	NA	NA
WP_152393742.1|2714224_2715022_-	HAD-IA family hydrolase	NA	NA	NA	NA
WP_152393743.1|2715058_2715577_-	hypothetical protein	NA	NA	NA	NA
WP_152393744.1|2715625_2715826_-	DUF896 domain-containing protein	NA	NA	NA	NA
WP_152393745.1|2715934_2716297_-	LysM peptidoglycan-binding domain-containing protein	NA	NA	NA	NA
WP_152393746.1|2716478_2717105_+	transcriptional repressor LexA	A0A1B2APZ1	Phage_Wrath	4.3e-15	59.4
WP_152393747.1|2717244_2718006_-	N-acetylmuramoyl-L-alanine amidase	G3MB93	Bacillus_virus	7.2e-33	42.2
WP_152393748.1|2718267_2718744_+	hypothetical protein	NA	NA	NA	NA
WP_152393749.1|2719808_2720000_-	peptidoglycan DD-metalloendopeptidase family protein	A0A1D6X855	Bacillus_phage	2.9e-07	54.3
WP_152393750.1|2720254_2720623_-|holin	holin	NA	NA	NA	NA
WP_152393751.1|2720848_2721196_-	hypothetical protein	NA	NA	NA	NA
WP_152393752.1|2721207_2722947_-	hypothetical protein	S6B1J7	Thermus_phage	3.4e-22	32.0
WP_152393753.1|2722951_2723566_-	DUF2313 domain-containing protein	S6BFJ0	Thermus_phage	5.2e-58	62.6
WP_152397217.1|2723884_2724832_-	DUF2793 domain-containing protein	A0A0S0N9R1	Pseudomonas_phage	1.1e-14	45.8
WP_152393754.1|2724916_2725330_-	phosphoglucomutase	A0A0A7RW10	Clostridium_phage	2.4e-35	55.7
WP_152393755.1|2725333_2726368_-|plate	baseplate J protein	S6AVU3	Thermus_phage	5.1e-98	54.5
WP_152397218.1|2726360_2726660_-	DUF2634 domain-containing protein	A0A0K2CP95	Brevibacillus_phage	1.4e-19	52.2
WP_152393756.1|2726755_2727112_-	DUF2577 domain-containing protein	S5M5M4	Brevibacillus_phage	4.7e-19	46.2
WP_152393757.1|2727108_2728062_-	hypothetical protein	S5MNC9	Brevibacillus_phage	5.5e-99	52.8
WP_152393758.1|2728075_2728762_-	LysM peptidoglycan-binding domain-containing protein	A0A0K2CNM3	Brevibacillus_phage	2.0e-42	41.7
WP_152393759.1|2728758_2730564_-	hypothetical protein	S5MNW9	Brevibacillus_phage	1.2e-113	39.0
WP_152393760.1|2730774_2731197_-|portal	phage portal protein	X5JAB6	Clostridium_phage	3.1e-25	42.5
WP_152393761.1|2731212_2731680_-|portal	phage portal protein	A0A0A7RVP1	Clostridium_phage	1.2e-41	53.3
WP_152393762.1|2731692_2733021_-|tail	phage tail sheath protein	A0A0A7S087	Clostridium_phage	1.0e-95	44.0
WP_152393763.1|2733187_2733625_-	hypothetical protein	NA	NA	NA	NA
WP_152393764.1|2733895_2734321_-	transcriptional regulator	A0A0C5AJ96	Bacteriophage	4.4e-24	45.5
WP_152393765.1|2734656_2735091_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_152393766.1|2735101_2735515_+	ImmA/IrrE family metallo-endopeptidase	A0A2P1JU12	Anoxybacillus_phage	3.1e-22	40.2

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP045293|3001221:3010073|DBSCAN-SWA
GTCAATCGAACGCTGTGAACAAAGCATTAAAAACCGCTCTAGCAACATCCACCAAGCTTCCCCGAGCTTGAGATGATGAATGACTAACATAAGCTGTCTTTCCTTGCTCATTGGCGAACACAGATCGATCCTTTGTTCTTAACAACGCGCTGTCCTTCTCATACAACGGAATAACGCCTAGCTGCTTCGTCCCAAGCATCACGAACAGCTTCCCGCGTTCTCCAAATGTGTAATCCATCGATGTACGAACCGTGAGTACAAGCTTGGTTCGGACCTGTTCCATTTCCCCTTCAGCGAAAGGATAAGCGAATGACTTCCCCACCTGGTAGGGGTAGTTCTGCACACCTTGTCCTTTCTGATAAATATCCTTGAGCGGGAAATGCTCAAAGCCGTAATCTAGCATATGTTTATGGTCTACCCAGTCCGTCCCATCATTCAACGTAACTGCAACAAGCTGTTGACCTTGGCGGGTCGCCGAACTGACGAGACAGCGAAGCGCTTTTTTGGTATAGCCTGTCTTTACGCCATCCGCACCCTCATACATTTGCAGCATCTTATTTTTGTTCAACCAACTATAATCCCATTTATCATTCGGATTAGGCGCTTTCTTCACTTTCGTCTTCACAATATCGCGAAAAATGGGATTCTTAAGCGCATATGCCGTAAGAACGGCCAAATCATTCGCAGAAGAATAATGACCTTCCGCATCCAGGCCATGAGGATTCATGAAATGGCTGTTATGCAGCCCTAACATTTCTGCCTTCTGATTCATCATGTATACGAATCCCTCTTCCGAACCGCCAATATGCTCAGCGATAGCCGTCGCTGCATCATTGCCAGAACGCAGCATGAGTCCGTACAGCATGTTCTCCAGCGACATTTCCTCACCAATCTTCAAATAGATCGATGAGCCTTCCTTACCTGATGCGCGTTTGCTGACTTCCACCTTATCAGACAATCGTCCATGTTCGATGGCGACAATCGCTGTCATTATTTTCGTCAAGCTAGCAATACGCATGGGTTCATCGCCATGACTGCTCCATAATATACGCCCCGACGTAACATCAATCAGCGCAGCTGCCTTTGCATTCGTCTGGACTCCCGAATCTATTGTTCGATTTCCTGTCGCCCAAGCAGAAGCACCTGAAATTCCCCAGAATAATACGAAGAATATCATCATCTTCGGTAAACTTATGGCCTTTCTCATTGTCGCCCTCCGTGTTATAGGTTCCTTGTCTTCTCATCTATATGCTTATCCACATCAGAGTATGTCCTAATCAAAAGATCTGTATCCTTAAAAAGGAATGTTACTATTCATCCTTATTGCACCCATACGATAATTATGAGAAAACCTCTATCGAAGCCTTTCGAAGATGAATTCTATTGTGGTTACAAAAAAACCGCCTCGCGCTCATCGTGCAGCGAAGCGGTGTTCTTGTTAACTCGAGAAGTTCGAAGGAGGCATATATCCACTCGGTTCTGGCGGATTCATCGTCGAATTCGCACTGGACTTTGCATTTGATTTATTCTCCATCATCGTCTGATACTTCTCCATAAATTGCGGGATCGAATCGATAACCCGTTCAACAAGATGTGTCTGATTATCCAGAGATACGATACGCACGCCATGCGTTCCTACAACGAGGAATGCAATCGGTGTGATGGATACACCACCGCCGCTGCCGCCACCGAATGGAAGCGCAACATCGGCATGATCTTGTTTTAGATCGTTCGATTTGGCTTTAGTCCGATCATCCGTTTGGAACTCACTTCCCCCTGCAGCAAATCCGAACCCGACCTTACTGATCGGAAGAATAATGCTGCCGTCAGGTGTTTGAACCGGCTCGCCAACAATGGTGTTAACTTCCACCATTTTCTTAATATTTTCCATTGAAGTCTGCATTAGGCCTTGAATAGGATGCTCTGCCACAACTTCAGTCCTCCCTTCACTCTCACAATGCGTACAAGAAGTACAACGCCTGCAATCATAGCGTGTCCGAAGCGAATTTTGGCTATGCAGCGCAATTCAGTGGTAAATTGCGGGTCATTGAAATGGGTATGTACTTGAAGCTGAGGCATATGCTCTAATTGAATCGTATGGGATAACCAGCCGGTTATGGTTCCCTTCATAGCCCAGACGATCCCCGTAGCCATTCCTGTCTCTACAACATCCCCGAACCCGATATGTGTCTCCCACGTTAGAACATCACAATGCACATGACGGAGCAGCTTCCTCACCCAGCGCTTGAAATCCGCTGTAAACCGAATAATGAGTGCGATTTGATTGTAAATGTGCTGAATGAATTCAAAATTGATAGAGATATGTTCGCGGGAATCATGACCATGCAGAATATTATCCTTTTCCTTTCTTTTCATAAGAAAGCCTTGATCGAACCCCTTGAACTTGATTTGTCGGATCTGATAATTCAATTTCACGAGTCCGAAGAGCATTCGCACCTTAATGGTGAAGTAATCATCTTTCTCCACTTTATTGAACAAAATCTTGATATCGATATATGTACATGCTGCGATGAGCAGCGCAACGAGAATACAACCTATGATGCCAATAACAATCCAGATCCACACGAGCAAGAACCCCCTGACTCTAATTCCCTCCGGTTAGAGGTAGTTCAAAAAGTCATCATTTGATCACGAAGTCATTCGAAGAAACATGATCGGCATCGAATCTTACGTTCACCTTCGAAGTCCGGTACTCATTTAGGTTTTGCCTAAACTCCGTTCCTCCTTCTTCAGGTTCTCGCAACCTTCTCGGTGCTGAAATGCCAACTTTTTGAACACGCACGGTTAGTATGGCTGAATTACATTCTTTTCATGACAAAAAACAGCCTACCACGGTTCAACCGAGATAGACTGTTCTTGTGAGACGTTCTATTTCATATCATCAATCGTCATTTGACGACCATCGAGCTTCTCGAAGAGCAACTGCGTCTCTTCATCCAGATCCATTTCACTCTCAAATTGGGAAGAATCGGGCAATCCCTTAAGACTATCGAGTCCAAAATAATCCAAGAATGATTTCGTCGTTCCATAGAGGATCGGACGGCCTATTGCTTCCGCACGTCCAACTTCCTCAATTAAATCTTTGGCGGTCAACGTCTGCAGTGCACGGTCCGACTTCACGCCACGAATCTCTTCAATATCTACACGCGTAATCGGCTGCCGATAGGCAATAATCGATAACGTCTCCAGTGCCGCTTGGGATAAGGTTGAACGTGAAGGCGAATAAGCCAATCGCTCAAAATAGGGTGCGTGCGCAGGTAATGTCGTTAATTGAAAAGCACTTGCAATCTCCGTAATCTGAATGCCTCGCTTGTTGCGTTTGTAATCCCCCTTCAAATCATGGATCACATCCAATACCAGATCAAGCGGCTGTTCGACGACTTCGGCGATCTGCTTTGCAGTTAATCCTTCGTCGCCCGCAACAAATAGTAGTCCTTCAATAATTGATTTCATGGTCTTGAAGTCCATCGATGCTCTCGTCCCCCTTCCATTCGATCACAATATCATCAAATAAATGGTCTTGATAACATCGGATCTGTTTCATCTTCATCAGCTCTAAGATGGCTAGAAAGGTTACGACAATCTCATGCCGGTCCATCTCTTCATTTAGCAGCTTCGAGAATAATACTTTACCGCCTCTTCCTACGCGATGTAAAGTAGTAACGACATCTCGAATACGATCTTTCACAGAAATTTCATCACGCTGGATTCTTGCAACGGTATTGCGACGCGTTGCTTTACGTAGTGCCTTCTGAAAAGCTCTGACCAGATCCGCCGTATGAAGTCCTTCAACAGGATTTTCGATTACCGTTGGCATGAAGGGTGTTAAATCCTCCGGTTCGCGAGAGTAAATCAAGCTTCGCTCGAATTCTCTCTCCCGAAGATGGTCTGCAATGCCTTTATACTTCCGATACTCAATCAGCTTCTGAATCAATTCCGCGCGTGGATCGAGCTCATCCTCAGGATCCATATAAAAATCTTCTTCCCATTCAATAACCGGAGGTTTCGGTAGCAGCAGCTTGCTTTTCATGGAGAGAAGCGTTGCCGCCATCACCAGAAATTCGCTCGTGACATCGAGTTCCAGCTCCTGCATCGTATTTAAGTATTCCATATATTGATCCGTAATTTCACTGATCGACACATTCTGGATATCGATTTCCGCCTTATCAATGAGGTGCAGCAGCAAATCGAGCGGTCCTTCAAATGTCTCCAGCTTATACGTTACCGTGGTCAAAATGACTTCCTCCCGCTTATCTTCTTACTAATAGATAAGCATTATTTCAACTGTTTCGTCAAGTTCGCCATTTCAATTGCCGTCACAGCCGCTTCCCAGCCTTTGTTCCCTGCTTTGGTACCCGCACGCTCAATGGCTTGCTCAATACTATCCGTTGTGATGACACCGAAGATGGTAGGGATACCTGTCTTTAAGTTAATGGCGCTTACGCCTTTCGCAACTTCGCTGCATACGAAGTCAAAATGAGGTGTCGAACCGCGAATCACTGTACCGAGTGTAATGACGGCATCATATTTACCGCTCTCCGCCATTTTCTGAGCGATGAGAGGAAGCTCAAATGCACCAGGAACCCAAGCGACATCAACCTCTTGATCTTGGGCCCCGTGACGTTTGAGTGCGTCCAATGCGCCGCTCAACAATTTCGTTGTGATAAATTCATTGAACCGTCCAACAACAACCCCATATTTTAATCCTGTCGATACTAAATGTCCTTCGAAAATGTTAGCCATGCTTCAACAATCCCTTCTTTTTATCTTCTTTTCTCATGCGATGATTTTATCGTCAACACCTTATTTGACTTCATTCTGCTCGACATCATCGAACTTCAGCAGATGACCAAGCTTCGATTGCTTCGTGTGCAAATATTTGGTGTTATCTTTGTTCTCCTGCATCTGGATCGGGACACGCTCAATGACTTCAAGTCCGTACCCTTCCAGCCCTTTAATCTTACGCGGATTATTCGTGAGAAGACGAATTTGCCGAATGCCAAGATCCTTCAGAATTTGTGCGCCAATTCCGTACTCGCGAAGGTCGGCGGGAAAGCCTAACTTCAGATTCGCTTCCACGGTATCTAGCCCTTGCTCCTGTAATTTATACGCACGGAACTTATTAATGAGCCCAATGCCACGTCCTTCTTGACGCATATAGAGCAATACGCCTTGGCCCTCTTGCTCAATTTGACGCATCGCTGCCTCGAATTGAGGCCCGCAGTCACAACGATGGGAATGGAATACATCCCCTGTCAGACATTCGGAGTGAACACGAACGAGCACAGGCTTCGATGGATCTATTTCACCTTTCACGAGCGCGATATGTTCTTTGCTATCCACTTCATTCGTGTAAGCAACGGCATGGAACTCACCGAAATCCGTCGGGAGCTTCACTTCCACTTCGCGTTTGACCAGCTTATCTTTCTCGTTCCGATAATGGATCAGCTCTTCGATCGTAATTAGCTTCAGATCATGCTTCTTCGCAATCTCGACGAGATCCGGAAGTCTAGCCATCGTGCCGTCTTCTTTAATCACTTCACAGATCACTCCAGCAGGATAGGATCCGCATAAGCGAGCCAAATCAACGGCTGCCTCGGTGTGTCCTGCACGGCGCAGTACGCCGCCCTTCTTCGCAACAAGCGGGAACATATGGCCCGGTTTACGGAAATCTTCTGGCTTCGATGCCGGATTGATCAATCCCTTCACCGTGCTCGAACGTTCAAAAGCCGAGATCCCTGTTGTCGTATCCACATGATCTACAGAGATGGTAAAGGCGGTGCCATGATAGTCGGTATTATGGGATACCATGGGCGCCAAATCTAGCTCTTCCGCACGCTCTTCGGTGATCGGCACACAGACAAGACCGCGTCCTTCCGTAATCATGAAATTAATGACATCGGGAGTCGCTTTCTCTGCAAGCGCAATGAAGTCCCCTTCGTTCTCGCGATCTTCATCATCCACGACGATGACAACCTTCCCCATCATCAGATCATATATAGCTTCCTCAATCGGATCGAACCGATAACGTTCTTCACTCATCTCTCCATCACCTTCACTTTCTTCTTGATTAGATAAACCCATTCTCCGCTAGAAATTGTTCCGTTACGCGATTTGCAGGTCTCGCTTGATCTCCGCTTGAACGATAATGCAGCAGGTGATCGACATATTTGCCCAGCACATCGCATTCGATATTGATGGTTGCTCCCGTACCCTTCTCCTGCAGCACCGTCTCAGCCAAGGTGTGAGGGATGATGGATACAGAGAAGACGCCATCTGCCTGATCAGCCTTCACCACCGTCAGACTAATACCGTCCAATGTGACAGAACCTTGCGGGATAATAAATTTGAACATGGAAATCTCATCTGGTCTGATCCCGAATACGACGGCATTCGCGTCTTCCGATCGGCTAATAATTGTCCCCGTGCCATCGGCATGCCCTTGCACAATATGACCGCCAAATCGTCCATTCGCTCGCATGGCTCGTTCGAGGTTAACTCGACTCCCAGGTTTTAACTGAAATAGATTGGTATGGCGGAAAGTCTGGGGCATCACATCCACGGAGAAAGACCCCTGGTCATAAGCAACGACCGTCAGACAAACCCCATTGACAGCAATACTGTCTCCAAGCTGCACATCATCCATAATCTTAGAAGCTCCAATATGTAAGATCATGGCTTCCCCTTTGCGATAGATCCGCCGCATGGTTCCGATCTCTTCGACCAATCCCGTAAACATCGTATCCTCCTCCTTCCATTCAATCCTTCGTATGACATTAAGCTTGAGCAGGGTAACCTGTTATACAGACATTATCTCCGAGCTGCTCCACCGTTAATTTCTCTAATACGATCGCTTCGCTCATCTTCTCGTATCCTTCGAAGACGATCGTACCCGGAGCCATAAATCCTCCAATAATCTTCGGTGCAAAGAAGAGCATGACCTTATCCACACAGCCCGCCTCGAGCATGGAGCCGTTTAAGCGGCCGCCACCTTCCAACAGAATTGAGCTAATCTCAAGCTCACCCAATCGTTCCATCGCGAGCGCCATATCAACATGTTCGCCAGATCCACATCGGATGATTTGTGCCCCTAGTGCTTCTAACTCCAGTACCCGTTCCTGGCTTGCTTGATCCGTCGTTAGAATCATCGTTGGCGCAGTGCCATCCTGAAGAACCTTAGCTTCTCGTGGAATGCGAAGCTTGGAATCCACAACGATTCGGGTCGGATGAAGACCCGGGACTGACAGTCTCGTCGTCAGGCTTGGGTCGTCTGCAAGTACCGTACCGATCCCGACCATGATCCCTTGATGCTGATGTCGCAACGTATGCACGATTTCACGAGCTGCCTCATTCGAGATCCACTTGCTGTCGCCCGTCTTGGAGGCTACTTTGCCATCCAACGTGCTCGCCGTCTTCAACGTGACGAATGGGCGTCTCGTCGTTATATATTTAATAAATTTTTCATTGAGCTTGATCGCTTCAGCTTCTAGAACTCCTACCTCAACTTCAATCCCATGGGACCGAAGCATTTCAACCCCTGTTCCCGCAACTTGTGGATTTGGATCTAGACAAGCAACAACGACGCGGTTAACCCCTTCACGAATCAATCGTTCGCTGCATGGCGGTGTCTTGCCATAATGACTGCAAGGTTCCAAGGTCACGTAAGCCGTACTTCCTACGGCCTCTGCTCCTGCCATATTCAGTGCATGAACCTCTGCATGTCCTGTTCCACGCTGCAGATGTGTGCCTAGCCCGACTACACGCCCGTCCTTCACAACAACGCATCCTACGACAGGGTTAATTCCTGTCTGGCCGACAGCTCGCTCAGCCATTTGAAGTGCAAGTCGCATATAAAATGCATCATTCATGACTTCCACCCTGATCCCCACCTTTCTCTCTCCAGTTCTCTTCTCTACATAGCATGGCAAAAAACCCCTTGGTACATGCCCAAGGGGTTGTAGAAGTTCGGTTCAACGTGAGACTAATCCCTATGAAGCGAATCCAGATTCATCAGCAAATAGACGTCACCAAATAGAGTCTACGCGATAGCCTTTTGTTAAAAAAGCGCGTGTACTCTCGCAGATTCGATTCTGTGTCTTACGTTTCCTTCTCCCATCCAGACTATACTGTCGGTCTCGGATTCTCACCGAGTCAGCCTTCACCCGTCTTGCAGCCAAGACATGGATCCGGGTCACGGACTTTACGAGTCTTCTGCTCGTATCACCGCCGGTTGGGATTTTCACCCGACCCCGAAGGAACATCACATTTTCTCCCACAGCTTATCATCTGCGCTTACAAAAAGCAAGCACATCCATCACTGCATGTATTACAGTAAGATGTTATGGCGACATGTAAAAACCCCGCAGGCCAATGCCTACGGGGTCTTCTGTCTTGCGACAATTAAACTTCTGTTACTTCCACTGTTTCCATACGATCTTTGCCTTTGAATGTATCAACATGCTCCATGCCTGATACAACTTTACCAAATACCGTATGTTGTCCGTCCAAATGCGGTTGCGGTTGGTATACGATATAGAATTGGCTTCCGCCTGTGTTACGTCCTGCATGTGCCATTGCAAGCGCACCGCGCTCATGTTTGTTCGGGTTGATCTCGCAATTGATTGTGTAACCAGGACCACCAGTTCCGTTACCTGTTGGGCAGCCGCCTTGTGCAACGAAGCCAGGAATTACACGGTGGAAAGTAAGTCCGTTATAGAACCCTTCGTTTGCTAGTTTTTCAAAGTTCGCTACTGTATTCGGTGCGTCTTTATCGAATAATTCAAATACGATTTCGGCGCCATTGGCCATTTTAATTTTTGCTTGTTTTGCCAT

Protein sequences of DBSCAN-SWA_2

>NZ_CP045293|3001221:3010073|3001221_3002427_-|WP_152394001.1|DBSCAN-SWA
MRKAISLPKMMIFFVLFWGISGASAWATGNRTIDSGVQTNAKAAALIDVTSGRILWSSHGDEPMRIASLTKIMTAIVAIEHGRLSDKVEVSKRASGKEGSSIYLKIGEEMSLENMLYGLMLRSGNDAATAIAEHIGGSEEGFVYMMNQKAEMLGLHNSHFMNPHGLDAEGHYSSANDLAVLTAYALKNPIFRDIVKTKVKKAPNPNDKWDYSWLNKNKMLQMYEGADGVKTGYTKKALRCLVSSATRQGQQLVAVTLNDGTDWVDHKHMLDYGFEHFPLKDIYQKGQGVQNYPYQVGKSFAYPFAEGEMEQVRTKLVLTVRTSMDYTFGERGKLFVMLGTKQLGVIPLYEKDSALLRTKDRSVFANEQGKTAYVSHSSSQARGSLVDVARAVFNALFTAFD
>NZ_CP045293|3001221:3010073|3004109_3004709_-|WP_152394004.1|DBSCAN-SWA
MDFKTMKSIIEGLLFVAGDEGLTAKQIAEVVEQPLDLVLDVIHDLKGDYKRNKRGIQITEIASAFQLTTLPAHAPYFERLAYSPSRSTLSQAALETLSIIAYRQPITRVDIEEIRGVKSDRALQTLTAKDLIEEVGRAEAIGRPILYGTTKSFLDYFGLDSLKGLPDSSQFESEMDLDEETQLLFEKLDGRQMTIDDMK
>NZ_CP045293|3001221:3010073|3007311_3007980_-|WP_152394008.1|DBSCAN-SWA
MFTGLVEEIGTMRRIYRKGEAMILHIGASKIMDDVQLGDSIAVNGVCLTVVAYDQGSFSVDVMPQTFRHTNLFQLKPGSRVNLERAMRANGRFGGHIVQGHADGTGTIISRSEDANAVVFGIRPDEISMFKFIIPQGSVTLDGISLTVVKADQADGVFSVSIIPHTLAETVLQEKGTGATINIECDVLGKYVDHLLHYRSSGDQARPANRVTEQFLAENGFI
>NZ_CP045293|3001221:3010073|3003122_3003806_-|WP_152394003.1|DBSCAN-SWA
MWIWIVIGIIGCILVALLIAACTYIDIKILFNKVEKDDYFTIKVRMLFGLVKLNYQIRQIKFKGFDQGFLMKRKEKDNILHGHDSREHISINFEFIQHIYNQIALIIRFTADFKRWVRKLLRHVHCDVLTWETHIGFGDVVETGMATGIVWAMKGTITGWLSHTIQLEHMPQLQVHTHFNDPQFTTELRCIAKIRFGHAMIAGVVLLVRIVRVKGGLKLWQSILFKA
>NZ_CP045293|3001221:3010073|3008017_3009118_-|WP_152394009.1|DBSCAN-SWA
MEVMNDAFYMRLALQMAERAVGQTGINPVVGCVVVKDGRVVGLGTHLQRGTGHAEVHALNMAGAEAVGSTAYVTLEPCSHYGKTPPCSERLIREGVNRVVVACLDPNPQVAGTGVEMLRSHGIEVEVGVLEAEAIKLNEKFIKYITTRRPFVTLKTASTLDGKVASKTGDSKWISNEAAREIVHTLRHQHQGIMVGIGTVLADDPSLTTRLSVPGLHPTRIVVDSKLRIPREAKVLQDGTAPTMILTTDQASQERVLELEALGAQIIRCGSGEHVDMALAMERLGELEISSILLEGGGRLNGSMLEAGCVDKVMLFFAPKIIGGFMAPGTIVFEGYEKMSEAIVLEKLTVEQLGDNVCITGYPAQA
>NZ_CP045293|3001221:3010073|3004677_3005475_-|WP_152394005.1|DBSCAN-SWA
MTTVTYKLETFEGPLDLLLHLIDKAEIDIQNVSISEITDQYMEYLNTMQELELDVTSEFLVMAATLLSMKSKLLLPKPPVIEWEEDFYMDPEDELDPRAELIQKLIEYRKYKGIADHLREREFERSLIYSREPEDLTPFMPTVIENPVEGLHTADLVRAFQKALRKATRRNTVARIQRDEISVKDRIRDVVTTLHRVGRGGKVLFSKLLNEEMDRHEIVVTFLAILELMKMKQIRCYQDHLFDDIVIEWKGDESIDGLQDHEINY
>NZ_CP045293|3001221:3010073|3006044_3007283_-|WP_152394007.1|DBSCAN-SWA
MSEERYRFDPIEEAIYDLMMGKVVIVVDDEDRENEGDFIALAEKATPDVINFMITEGRGLVCVPITEERAEELDLAPMVSHNTDYHGTAFTISVDHVDTTTGISAFERSSTVKGLINPASKPEDFRKPGHMFPLVAKKGGVLRRAGHTEAAVDLARLCGSYPAGVICEVIKEDGTMARLPDLVEIAKKHDLKLITIEELIHYRNEKDKLVKREVEVKLPTDFGEFHAVAYTNEVDSKEHIALVKGEIDPSKPVLVRVHSECLTGDVFHSHRCDCGPQFEAAMRQIEQEGQGVLLYMRQEGRGIGLINKFRAYKLQEQGLDTVEANLKLGFPADLREYGIGAQILKDLGIRQIRLLTNNPRKIKGLEGYGLEVIERVPIQMQENKDNTKYLHTKQSKLGHLLKFDDVEQNEVK
>NZ_CP045293|3001221:3010073|3009641_3010073_-|WP_152394010.1|DBSCAN-SWA
MAKQAKIKMANGAEIVFELFDKDAPNTVANFEKLANEGFYNGLTFHRVIPGFVAQGGCPTGNGTGGPGYTINCEINPNKHERGALAMAHAGRNTGGSQFYIVYQPQPHLDGQHTVFGKVVSGMEHVDTFKGKDRMETVEVTEV
>NZ_CP045293|3001221:3010073|3002658_3003150_-|WP_152394002.1|DBSCAN-SWA
MAEHPIQGLMQTSMENIKKMVEVNTIVGEPVQTPDGSIILPISKVGFGFAAGGSEFQTDDRTKAKSNDLKQDHADVALPFGGGSGGGVSITPIAFLVVGTHGVRIVSLDNQTHLVERVIDSIPQFMEKYQTMMENKSNAKSSANSTMNPPEPSGYMPPSNFSS
>NZ_CP045293|3001221:3010073|3005516_3005984_-|WP_152394006.1|DBSCAN-SWA
MANIFEGHLVSTGLKYGVVVGRFNEFITTKLLSGALDALKRHGAQDQEVDVAWVPGAFELPLIAQKMAESGKYDAVITLGTVIRGSTPHFDFVCSEVAKGVSAINLKTGIPTIFGVITTDSIEQAIERAGTKAGNKGWEAAVTAIEMANLTKQLK

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_152394001.1|3001221_3002427_-	D-alanyl-D-alanine carboxypeptidase	A0A1P8VVG5	Erythrobacter_phage	4.8e-07	30.9
WP_152394002.1|3002658_3003150_-	sporulation protein YtfJ	NA	NA	NA	NA
WP_152394003.1|3003122_3003806_-	DUF2953 domain-containing protein	NA	NA	NA	NA
WP_152394004.1|3004109_3004709_-	SMC-Scp complex subunit ScpB	A0A1B1IVT7	uncultured_Mediterranean_phage	6.9e-15	31.5
WP_152394005.1|3004677_3005475_-	segregation/condensation protein A	A0A1B1IVW1	uncultured_Mediterranean_phage	3.1e-10	39.5
WP_152394006.1|3005516_3005984_-	6,7-dimethyl-8-ribityllumazine synthase	A0A2H4PQS3	Staphylococcus_phage	6.1e-43	56.3
WP_152394007.1|3006044_3007283_-	bifunctional 3,4-dihydroxy-2-butanone-4-phosphate synthase/GTP cyclohydrolase II	A0A2H4PQS2	Staphylococcus_phage	3.1e-118	52.9
WP_152394008.1|3007311_3007980_-	riboflavin synthase	A0A2H4PQS5	Staphylococcus_phage	3.5e-39	44.7
WP_152394009.1|3008017_3009118_-	bifunctional diaminohydroxyphosphoribosylaminopyrimidine deaminase/5-amino-6-(5-phosphoribosylamino)uracil reductase RibD	A0A2H4PQS8	Staphylococcus_phage	3.3e-55	37.5
WP_152394010.1|3009641_3010073_-	peptidylprolyl isomerase	A0A1B1IVS0	uncultured_Mediterranean_phage	1.4e-20	44.2

Sequences of DBSCAN-SWA_3

Nucleotide sequences of DBSCAN-SWA_3

>NZ_CP045293|4914172:4931045|DBSCAN-SWA
CTTACTCACCTAAGCGTTCACCGTATTGCTTGGCATAGTATTCTTGGTAGGCACCTGATTGAATCCGAGTCCACCATCCTTTATTGTCTAGATACCATTGAATGGTCTTCTGAATTCCCTTTTCGAAAGGATACTGCGGTTGCCAGCCTAGTTTGGCGCGGATCTTCGTCGCGTCAATCGCGTAACGGCGGTCATGGCCAAGTCGATCAGCTACGTAAGTAATCAGTGATTTCGGTTTACCAAGAGCCTCAAGAATGGTCTCTACAATCTGAATATTCGTACGTTCGTTATTCCCGCCAACGTTGTATACCTCGCCGCTGACGCCTTTATGAATCACGAGATCAATGGCGCTACAGTGATCCTCGACATATAGCCAATCACGAACATTCAAACCGTCCCCATAGACTGGGAGTTGCTTATCATTCAGTGCATTCGAGATCATTAATGGGATTAGTTTCTCAGGGAAGTGATATGGCCCATAGTTATTCGAACAACGAGTGATATTCACATTCATGCCGTAAGTCTCGTGATATGCACGCACCAGCAAGTCCCCACCCGTCTTACTTGCCGAATATGGGCTGTTGGGCGCAAGAGGAGTCGTCTCCGAGAACAGACCGGTATCCCCCAGTGTTCCGTAGACTTCGTCCGTAGAGATTTGAACATATTTGTTCACATTATATTTCCGAGCTGCATCGAGCAATACTTGCGTTCCCATGACATTTGTCTGCACAAAAATGCCTGGGTCCAAAATACTGCGATCCACATGCGACTCCGCTGCAAAGTTAACCACAACATCGATTTGATGCTGCTGGAAGATCTCTTCTACTTTGACTGCATCAGCGATATCACCTTTAATAAAAGTGTAATTCGGTTTATCCTGAACACTTGTTAAGTTCTCAAGATTCCCCGCATACGTAAGTGCATCGAGGTTAATGATCTGGTACTCAGGATATTTATTCACCATATAGATCACAAAGTTACTTCCGATAAATCCGGCCCCGCCGGTAACTAAAAGTTTCAACACGGCTCCTCCTCAATCAAAGTTGATGTCCGCATCACGCAGAACGGGATGCTTCGTATCTTTATCAGATAAGATCGGCTGTTCTACCGGCCAATCGATGCCTAACGCAGGGTCATTCCACAAAATACCTCGATCATGCTCAGGGGAGTAAAGTGCGTCTACTTTGTAGAGTACCTCCGTGTTGGCTTCTGTGGTACAGAAACCGTGAGCGAAGCCCTGCGGCACAAGTAGCTGACGCTTATTCTCAGCACTTAAATGTACACCCACCCACTGGCCGAAAGTTGGCGAGTTACGACGAATATCTACAACCACATCATAGATTGCACCAGCAGCGACACGGACAAGCTTCGTCTGTGCTTTAGGATTCAGTTGGTAGTGCAACCCGCGAAGAACACCCTTCTCCACAGATAGTGAATGATTGTCTTGGACGAACAAATAATCCATATTATATTCACGGAACTTCGCACTGTTGTAGCTTTCCATAAAAAACCCGCGATGGTCCCCATGGACCGCGGGTTCAATGATTCGAACGCCTTGTAGTTTTGTATCGATTATGTTCATGAACTTACACCTCTACAATTTCAATTTTCCAAACTCTTCGGAAAAGGTGATGTTCTGCGCAAGCTCATTTGCTTTAGCCCAAGAGACATGCGTACCAGCATCTGTCCACCAGCCTTGAAGGACATCATAAGTAAGCTCGCCACGTGCGATGTAGGCATTATTTACATCCGTAATTTCCAATTCACCGCGACCAGATGGTTTTAGTGTTTTTACGATATCGAACACAGTACTGTCAAACATATAAATTCCTGTCACTGCGTAGTTACTCTTTGGTGCTCTCGGCTTTTCTTCGATGGAAACAATGTTGTCTCCGTTAAGTTCAGCCACCCCGTAACGTTGTGGATCATGTACTTGTTGAAGAAGAATTTTCGCGCCTGTTTGTTGCTCACGGAAGTTTGCAACATATCCAGAGATGTCATCTTCGAAGACGTTGTCTCCGAGAATAACAACCATTTGATCATCGCCGACGAATTGTTCCGCTAGATCAAGGGCTTGTGCAATCCCACCGGCTTCATCTTGTACTTTATAAGTAAATGTAACGCCCATGTCACGCCCACTTCCTAGAAGGTTTACAACGTCGCCCATGTGTTCTTTACCGGTGACAACTAGAATATCATTAATGTCTGCTTGCATTAACTTATTTACAGAATGAAAAATCATTGGATATTTACCGACCGGTAATAAATGTTTATTTGTGACTTTTGTTAGTGGGTACAGGCGCGATCCAGTGCCTCCTGCTAAGATAATACCTTTCATAACTCCACCTACTTTTCATTTACTCAAATAATTTCTTCTTAATTATTTGTAGCTTTCACTCTGAATACAAATCTCTTATTTAATATATATGACACCATAGACATTGGTAGGATCAAAATCGCGTACGCTATATAGATACTCACAAATTCTTTTAAAAACGTTAATAATGCTAAATTTAATAAATATGTTACTCCATATGTTATGAAAAACTTAATTATCAAAGAATTATCACTACTTTTAAATACAATTCGTCCTGTAGTTTTAAAGTTAAAAAGAATTCCAACAAGGGTAGACAATAAAGATGCTAATGTATAATGCAATCCTACAAAAATAAACAACGAGAAAACAGAGTAGCCAAAGATTGTATTTATAACACCAACTATAATAAATTTTACGAATTGATTGTCCATTAGTTACTCCTTGGCCTTTACTGAATTAACCTTTTACTCTCTCTAGTTCTTGATTGATTATGGTTTCGAAATTTATTCGCTCTTTTTCTACAACCAAAGGCCTCTTCAATACCTGTGTATGAATGGAACCAATATATTCCCCTATAATTCCAATAAAAAATAATTGCACAGAAGAAAATAAAAATAGACCTATCACGAGAGGTGCCAGCCCTAGCGTGAAATAATTCCAGAATACTAGCTTTGCAATCAGATAACCCACTGCAACCAAAAGACTTACAGCTGACATTAAGAAGCCTAGCATAGCAGCTAATCGCAGTGGTATCTTAGAATGGTTTGTAATTCCTAGCATTGCCATATCATATAATGTATAGAAATTATTCTTGGTTATACCTCGTTTTCTAACAGGCTGCACATATTCTATTTTATAACTTTCAAAACCAATATCCGAAATCAACCCTCTAAAGTAAGGATATGGATCATTAATCTCTCTTAAGATCTGAATGATTTTACGATCATATAATCCAAACCCTGTGTTATTTTTCGTTAGTTCAATTTCAGATACCCTGTTAATAAAATTATAATACATTTTTCGAATCGCAAACATCGCAGCACTTTCATGGCTCTCCGTTTTTACACCAAGAACTACTTTATAGCCTTCTTCCCATTTCTCAATAAAGTCAATAATCATGTTAGGCGGGTCTTGCAAATCTGCAACCAATAAAATAACTGCATCCCCATCTGCTTGTAGTAATGCATGATAAGGAGAGCGTATATGTCCAAAGTTTCTGGCGTTAACGATAATCTTAACATTTTGATCCTTTAGTGCTATTCTTTTCAATATTGCAACCGTATTATCTTTCGAAGCATTATCGATGAAGATATGTTCATATACATAACCACTTAGTTCATCAAATACTTCTCTAACGCGCTGGTATAGTTCTTCAACATTGTCCTCTTCATTATAGCAAGGGGTTACTATACTAATTTTCTTCATTTTTCTAGCCTCATTCTAATATATTTATACTCATCATCAATACTCTCTATAGAGCTATACTGTGGGTGAAATCCTACATTTTGTGCCTTATGAAATTCTGAGTAGTAATTGTCCTTGTTACCTGTAACAGATGACTTCACATCCCCCTCAATAATTCTATAGCTCAATTGATGATTATCCTTAAAGTAATTCAGCAAATCAAATTTCGATATAGGGCATTTTGAATAAACGTCAAAAGCATCATTAACTTCAGGGTTATTGATAAGTCGTTCAATAAGTTGATTTAAGTCATGCGGATGAATGTAATCACGAATAATATTAGACGGACTAGTTACAAGCTCATTGCCAGTCCTAATACAGTTAATAATATCAGTCATGAGGAACTTTGAGTTTAGATCAATATACCTGCTAAAAAAGCCAAAAACTCTCAAATCGACAATATTATTCATCAATAAACTTCGATGCTTTGCTTCAGTATACAGCTTAGTTACACCATAATAATCTTTGGTTGAAAAACTATTAATCTTTACTTTATTCGAAGTTGTATATTCTACGGGCTTCATGAAATCTTCACCGTACGCCGCACCACTGCTAAAATTGATATACAATGTTTCTTGTGAATCACGAATCTTCTCTATAATCAAATTATCGAATGATTCTGTTAGATGAAAAATTTTATAAGGATCTTGCTGTAAATCTTGTGGATTTCCGATGCCAACGCAATTTATGATGACATCAAAAAACCGCTCCTTAAAATCATTTAAATCTAGTATGGTTACAACCTCTAAACGCTCCGCTTCAAGAAACTCTACTAACTTTGCCTCAGTACGCGCATATGCAAATATTTCATGCTCTTTCTTTAAACATAACCCTGTTATAATATTTTTGGCTATATGACCTGTAGCGCCTAATACCGCTATCTTCTTTTTAATCACCACCATCAATGGCTCCTTTATTTAGGGACTTCCATTTCTTCAACAAGATCAATGAGCATGACTTCCTTTAACTCTTCTCTATCTAAATGCGGCGACATATCTTCAATCGGACGATTTACAACCAACTTAGGTTGAACTTCTGTATTTTTTTGTAACATGACTTCTATAAAAGCAGGCCCTTCCTCAGCAAAAAACTGTTCGATCGTTGCTGTCTCGCTCAATGATCTAACTTGATATGAAGGAATGCCATATGCTTCGAAAATATCACCAAAGTTCGGATTCTCACTTACCGTCGATTGCTGTCTTCCATCAAAATATAAGTCTTGGAATTGTCTAACCATGCCCAGGCAATTGTTATTCATAACGCAAATTTTGACAGGCAAATTCATTCGTCTAAGGGTATCCAATTCTTGAATGTTTAGTTGAATGCCTCCATCCCCGGCAATAACGAGTGATTCCTGATTAGTGGCTAGCGTTGCACCAATTGCTGCAGGCAGCGCAAAACCCATTGCCCCCATTCCACCCGAGTTAAGAATACGCTGGCCATCTTGGAGTTTAAATGATTGAGATGCCCACATTTGATGCTGACCGACATCTAAACAGATGGCTTTAATTTTCCTTGCATATGAAGATAGTACACCCATAAATTGATTTGGTTCAATTATATCTGCTGATGTAATCCCAGATGAAGTCGGATATTTTGCTTTAAGTGTTTCGATCTTCATTAGCCAGTCTGATAGATCCGGCTTTCTATAATTTTTTAACTTGATATTCATTTGCTTCAAAAATTGTAATAAGTCAGTTTTAATTGCTATATCAACCTGTACCTTGCAATTCAACTCATTAGGGTCAATGTCAACGTGGATTTTTTTCGCTGCTCGTGCAAATGTATCGGGTCTTGTTCCCGTTTGCCTACTATCTAGTCTAGAACCTAGTATAATCAATAAATCACAGTTCGCTAACGTCATATTGCTATATCGATTTCCATACGAGCCAATTAACCCGCAATAAAGTGGATTATCATGTGAAATAACGTCAAGGCCCATTAATGAACTCACAACAGGTATACCGGTTTTCTCTATAAACAAACTAAGTTCTTCATAGGCGTTACTTACTCTCACGCCACCTCCCGCAAGTATTACTGGTCTCTGTGCGTTAGAAATCATTTCATATAATTGGGAGATGATACGAGCATCCAGAACATCGTTCGCCATTGATAACTCTTTGTATTCATCACTGTCAAAGAAACTCTCTAAATTACTCGGATCAATGTCAGCTCTTTGAACATTCATTGGGATATCAATCAGAACTGGCCCAGGTCTACCATTCTGAGCTAGATAAACGGCTTTTTCTAAAGAATATCTAATTTGGGATGGGTCAGTTACTAATGCTGCATACTTCGTGAGTGGTGTTACAACACTTACGATATCCGTTTCTTGAAATCCAATTTGTCGAACAGGTCTATCAAATTTATATTCATATGTATTTACCTGGCCTGTTACAAACAAACAAGGAACTGAATCAAAGAAACAGCTCCCAATCCCTGTCAATAAATTCAACGCCCCCGGGCCGCTAGTTGCCATAGCAACGCCAAGTTTTCCATTCATTCTGGCATATGCTTCTGCTGCAAAAGACGCTGCTTGCTCATGGCGAACCGAGACACATTCGATATCATCTCTTTTTGCAATCGAATCTAAGAGATGTGCAATTGCTCCACCTATAAATTCAAATACATGTGAGACGCCTTCTTTTTTTATAAAATCAATAACGTAATCAGAAAGCTTCATAGCGCATCTCCAATCTAGATCAGCTTTGATATTCCTTAATATGCTTTATACAAACTTCCCGCATATTTTCGTTGTTTCGATATGCCTTAGTCCAACTAACAATTTTCTCAATTGCCGTTTCCAAATTCCAGCGTGGCGACCAGTTCAATATAGCATTCGCTTTAGAACAGTCCAACTTTAAGTACTGCGCTTCATGCGGCTGTGGATTTGAATCAACACGATAGTTCGCTTCCGTTCCCCACTTATTACACATTTCTTGGACAATCCATTCGACTGGTTTGGCATCAATATCGTAAGGGCCAAAATTCCATGCTTCTGAATATTTCTCTCCATCTTCGAATAATTTTTCTGCCAGAAGCAAGTACCCTCCTAGTGGTTCTAAAACATGCTGCCAAGGTCTAATCGAATATGGATTACGAATAATGATCGTTTGATCAGCCATTAATGCCTTAATGCAATCAGGAATCAATCTATCTTTAGCCCAGTCTCCCCCGCCAATAACATTTCCAGCACGAGCTGATGCTACTCCTACAAATCTCTTTTCGTTATGGTAAAAAAATGAGTTTTTATACGCTGAGGTTACTAATTCAGAGCATGCCTTACTACTAGAATATGGATCGTATCCTCCCATAGGTTCATTTTCTCTATATCCCCAAACCCATTCTTTATTCTCATAACATTTATCTGTCGTTACATTCACAACAGCTTTCACAGAACTACAATTCCGGACTGCTTCAAAGAGATTAACCGTTCCCATAACATTGATGCTATAAGTATCCACAGGATTAATGTACGATTCCCTTACTAAAGGCTGTGCCGCCATATGAATAACGATTTCAGGAGATGAGAATTCCATAGCCTCTTGAAGCGACTTGCTATCTCTAATATCTGCGATAAAGCTTTTTTCAAGTATTTCATCAATTCCACAAACATGATACAGGCTAGGCTCCGTATTAGGTATTTGTGCATATCCGTATACTTTTGCCCCCATCGAATGTAACCACAACGATAACCAAGACCCTTTAAAGCCTGTATGACCTGTTATAAATACCCGTTTATTTACCCAAAAGTTTGTGTTTATCATACATTCACCGGATCCCGATCCCAAGTTTTCCATGGTGCTTTACCAGATCCCCACAAATCTTCAAGATAATTTTTATCTCTCAAAGTATCCATTGGTTGCCAGAATCCATCATGTTTATAGGACATTAACTCCTCATTCTTTGCCAGTGTTTCTAGCGGAGCTTTCTCAAAAATTGTGCTATCATCAGCAATATAATTAAAAATTTCGGGTTGCAGTACAAAAAAACCTGCATTGATCCATGAGTTATCACCTTTTGGCTTTTCCTGGAATCCTTTAACTAGATTATTCTCAGTAATATTAAGAGCGCCGAATCTCCCACTTGGTTGAACAGAAGTGACCGTCCCAATTCTTCCATGTAACTTATGATAATTAACTAACTCGGTAATATTCACATCCGATACCCCATCACCATAAGTCAGCATAAATGGCTCATCTTCGATGTAAGGTTGGATTCGCTTCACTCTCCCACCTGTCATCGTATCAAGCCCCGTATTGACTAATGTTACTTTCCATGGTTCTGCCGAATGATTATGTGTAATGATTTGGTTATCATTTCTAAAATCAAACGTTACATCGGACTCATGAAGGAAATAATGTGCAAAGTATTCTTTAATATAAAATCCTTTGTAGCCTAAACAAATCACAAAATCATTAAACCCGTGCTGTGAATACAATTTCATAATATGCCATAAGATAGGCTTTTGTCCGATCTCGATCATCGGCTTAGGCTTTAAGTGCGATTCTTCACTAATTCGAGTACCATATCCACCTGCAAGTATAACGACCTTCATTTAATACCCTCCTTCAAGCTAGACTAATTATCAGTTTTTGGAATACACAAATTCTTTGATTTTATCAATAACGTAATCAATCATCTCATCTGACAAACCTGGATAAACCCCTACGAGAAATGTATCATATAAGATTTTATCAGTATTTTTTAGGCCTCCATGAATTCTAAAGTTAACATTTTGATAAGCTGGCTGACGGATGAGATTTCCCGCGAATAACATGCGAGTTTGAATGCGGTTAGCTTCTAAGTAATCAACAATTTCATTTTTGGTGAAGTTAACTCCATCTCTTAATGTCAAAATGAAACCAAACCAGCTTGGATCCGAGTTCTCTGTTGCTCTAGGAAGAATAAAATATTGGTCGAGCTCCCTCAATCCTGCCAATAAGCGATTAAAGTTATTCTTTCTTGCCTGTACAAACGAAGGCACTTTCTTAAGTTGCTCTACCCCAATAGCTGCTTGCATATCCGTAACTCTCAAATTATATCCAATATGAGAATACGTATATTTATGATCATATCCATACGGCAGAGAGCCTAATTCCCAACCAAAACGTTTCTTGCACGTATTATCACAACCCGATTCACACCAGCAATCACGACCCCAATCCCTGAATGATTCAATAATCATCTTTAATTTAGGGTCATTCGTATAGACTGCCCCACCTTCACCCATCGTCATATGATGAGGCGGATAGAAGCTCGATGTGCCAATATGACCATGAGTACCCGTAAGTTTTCCGTTAAATGTCGAACCCAGAGCATCACAGTTATCTTCTATTACCCATAAATTGTATTTTTCTGCAATTTCCATTACCTTGTCCAATTCAAAGGGATTCCCCATCGTATGGGCTACCATAATCGCCTTAGTTCTTGGAGTGATTGCATCTTCAATACGATCAACCATGATGTTATATGTACCTAACTCCACATCAATAAATACCGGGATCGCCCCATTTTGAATAATTGGAGCTACCGTTGTTGGGAATCCCGCAGCTACAGTGATAACTTCATCACCAGGCATTACACGACGATCACCAAGTTTTGGCGAAGTAAGTGTTGAAAATGCCAATAGATTAGCGGATGAACCGGAATTCGTAAGTAGTGCATACCTTACACCTAGGAATTCAGCAAATTCTTTTTCGAATTGTTTGTTATATCGACCCGCCGTAAGCCAGAAATCAAGCGATGAATCTACAAGACTGCGCATTTCCTTTTCGTCATAGATTCGCCCGCCATAAGAAAGAGAAGATTTCTCAACATCGAATTTTTTGTTTCTATTAGAATGAAAAAGATCATAATAGTTTTCAACCTTTGAAAGGATTTCTAATCTCATTACCTTCTCAAAATCGTGCTCACTTAAATCAAAGATAAATTCAATATCATTTTTTAATACATGAAGTTTATCTCTCACATCTAAAAATAACGGCGTTTCTTTATTAACTTTTATTACTTCATGGAAATTTCCGTTTTGTATTTCTGGAGCATTTTTACTTAGTTTGAATACTTGAAATATATTTTCTAGTTCATATCCAATCAAACCATATTCACCTGTATTTTTAAACTTCACTATACTACCTTGTTTCAAATGCCTACACTCCTTTAAATATTTTAAGTATTCTTCAGCATCAATGATTAACATGGCCTTTAGAATATTATGTAAATAGTAGGTTAAATCATTTCATATTAGTTAACATAAAAAGCATTATTTTTTTACCTTTTCGATAGATGGGTCCTGGAATGTCCCTTTTTAAATAACTCACAATACGCTTACTTATGAACTTTAACGTTGGGCAATACCCAAATCCCCCAATGCAATCCAATCGGCAATATTATTTCCATTTGGTGACTCAACACCAAATGTAATATCAACATTTTTTCCAGAATAGCCCTCAATACTGATTTCTATTTCATTAAAATTGGATTCCTGCGTGACATTGCTTTCATAAATCCTACGCTCATTTCCATTATCATTAATGCTGATATAGAAATTTGCACCATCACTTCCTTTAAGGGGAAGTATTAAATCACCACAAATCTTCGAATCTGTAGGAATAAATATATTCTTATAGGTGTATTTAAATCCACTAATGATTGTTAACGTATTTATCTTTTGAAATTGTGTTGTCCAATCAAATATAAATACTCCTTCCCCATTAGGTGTATCTTCATTTACACTCTGTGGGGTTACCTCACCTTCATGGAAATGGTCGATAAGACTATATTTAATGTTTTTATTCTTACCTAGCGCTTTATTTTTATATAGAATCACCTCGTTGGTGACATTAATAAATCTCTTTTGAGAATCATTCAGTTTTAGTAAAACTACTTTTGTCGGATCAATCTTCGTGAGATCTACATCTAGTATGTTATCAACATATTCAACCTTAAACGTATCATCTCCCAAATAAGGTTTTAAAAACAATGAATCTAATAAAGGCCAATCTATATCCCGATGTTTTTCTATAAAAACTTTGTACTGCCTAATATTCGTACCATACTTTTTAATGGTCTCATCGTAGGCAGAGTCTGAAATCTGCTGAGAATACACAAAATATATATTATGGATATAATCCTTATAATAAGAATTTTGTTTAAGGTTACAACAAGTAAATAAAATCATCAAAATCATCATCAATTTTTTGGAATTTATCTTAGCAAAAAGATATCCCATGTATATAATGAATACTAAGTATGGGGTTTGCAACCATCTCAGTTCTTGATACACAGTAATTGATGAGACTAGCACTAAGGCGCATACAAGCATTAACATTATCAAAAATATTTTGAATTCAATCAATTTTTCTTTTTTATCCTTGCCTTTTATTGCTGCTATAAATACTATCATAGAGAGTATCAGTACTAATACTGATACTATTATTGTTGTTAAATTAACCTGATTTATCGGAATACCATTCAAGTGTTCTGGCCCTATATTAAACCCAAATAAATTTAATAGCCCTCCTATAAAAAACTTTATTACCGAATATACATTAATTTTGATACTTGTATAACCAGTCCCTACTAAAATACTTGATTTAAGAAAAAGCTTTTTGAACATCAGATAAAAAATGATTGGGGAGACAATTAAGCCAAATGCGATAATTTTCTTTTTCTTTTTCTTTTCATGTATTAAGTGAAAATGCATAAACAAAATTATTACTGGAATTATAGCTATAAATCTCTCATGTGTAAAAATAATTAAAAATTCCAGTATAAGTATATATAAAAAACCACTTTTTTTTCCTTTGCAGTATAATAAATACGAATTCAATATTATGAGTATAAGGAATAATGTACAAATAGCCTCCATCAATCCATAAATTTGCAATATATTATAGTAAGCAAAACGGGATGTAATAAAAAGTAAGGAAATAGCATAACTAATATACTTATTATTACTAATCAAGTTTAATAATTTATAAACAAAATAAATGATTATACAATTGAACGTAATATTAAACATAAAATACAATTGATAATTATTATCGAATAATTTATATAATATATATTGCACTAAATTAAACACAGGTCTGTATTTATCAGCGAAGTCATTTAATAAAACAGCCTCCAAAAAGGACTTTCCACGGAAAAAATCCCAACTGTTTAGATCATCACCCATAATCGTGTGATAACCACCTAATTTTATATACCAAAAGAAATTAATAATAAATAGACTACATAATAATATTTTATTAATTATATTTTCTTTCAATTCTAGCCTTAACCTATTCATAAATTTCTATGGCCTCCGCTGAATGTTCTGTTATTAAAGAGTAATGGATTCGGATGATATCACCCCAAATTAATATCACTATATAAACCAGGCTATTTATTCGCATTTATTTTCACATTCATTTGAACTAGTACATTTTCCCCGACTTCAGCTCTTATCCCCGCCTCAATATCACTATCTTTATCTCCAAACAATATTGACTCTCTCAAATCTATATCAAAATCATCTTTTGCTTGCAAAATCATTCCCGGGTTCGGTTTTCTACACCAACTATCCTTTTTATACTCCCCAATTCCGTGCTCTGGATGATAAGGAGAGTAGTAAACTTTAGTAATCTCAATCCCCTCCACCTTAAACCGCTCAATCATCCAATCGTTCAACTTGTGAAAATCCTCTTCTGAGTAATACCCTCTTCCAATCCCCGCCTGATTTGTTATCACAATTAGCAAATACCCCAAAGATTGAAAATGCTTCATTACATCAAATATTCCATCCACAAACTCAAAGTCTTCAATTTTATAGACATAGTTTTTCTCTACATTGATGACTCCATCTCTATCAAAAAACACGGCCTTATTCAAATTTAATCAACTCACTTTGAGCTTTATAATAATCTTCAGGAATACCAATATCAATAAAATACTCGTCTGCAATATATGAATTTACCTGGATCCGCTGTAGATGTTTCTGAAGGAAATCAGTCTCAAATGAAAAGGTCTTCTCAAGATTACAGCCATTAAAAATACTACGATTCAGTATATAAACACCACCATTGATATCACCAAAACTCGTATATTGTTTTTCTTGGAATTTCACTACTCGGTTGTTAACGTGATCCACCTTACCGTAACGTTCAAAGTCACTCATTGGTTTCAATGCCATCGTCATTTCCCCAGCCTGAGTTCTATGGAATAACATCATTTCTTTCAGATCAACATTAAAAAAAGTATCTCCATTAATTACGATGATATCTTCCTCTGTTGTATATCGCATTGACTGTGCAATAGCCCCTCCAGTACCGAGGGGCTCCTTTTCAACTGAATATTCAAGTCTCATAACACCCTGGAAGCACGAACCATAATAGTCTTCGATAACTTCATGCTTATATCCCGTAGACAACAAAACAGAACGAATGTCATACTTTAATAAATACTTAAGTAAGTAGGTTAAGAATGGTTGCCCATTAATAGGTGCCATAGGTTTAGGTACATCATTGACAGCACTTTGCAGTCTTGTTCCGAATCCTCCGGCAAGTATAATAGCTTCCATATTAATTAAATCCTTTCCCGAAAATGCTTTCTTCTACTACAGCACAAATAATATGTCCGATCAATATATGAGATTCCTGGATTCTCGGTGTTTCATCAGAAGGGACTTTTATACAATAATCACAGAACTCTTCCATTCTACCTCCGGATGCTCCTGTGAGTCCCACTGTGATAATACCTTTTTCTCTACATTCTTTCAATGCACTTATTATATTGGGGGAGTTGCCTGATGTTGAAATTCCAATAAATAAATCTCCCTCTGAACCCTGTGCCTGGATTTGTCTAGCAAACAATCGTTCATACCCGTAATCATTCCCTATAGCAGTTAATATTGAAGTATCTGTAGTTAGCGCAACTGATGGAATACCCGGCCGATCAAAATAAAACCGACTTACAAATTCTCCAGCGATATGCTGAGCATCGGCAGCACTACCTCCATTACCTGCTAGCAACGTCTTTTTCCCATTCCGATATACTACAGTTGTCTTTTCAGCAACCTCTTTGATGAGCTTTGTTAATTCAGTGCTCTCTAATATTAATCGCTTAATCTCATAAGATTCTTTTATCTGATTATTAATAAAACTTTGCATCTAATTAATCCTCCAACTCTCTGCACCGTTTTTCGTGAAATGGAAGTTCATTACAACACCATCTAATCTTTGAAGTTCCTTAATAAGATTTATTCGCTTTGCAGGATCAACCATAAACATCATAAATCCACCACCACCTGCACCGGATACTTTACCAGCATAAGCACCCGAAGCTATTGCGATATCATAAACCCTATCAATGGATTGGTTCGTTATCGTTGATGCTGTTCTCTTCTTTGCTTCCCAAGATTTCCCTAAATAGTTTGCGAACGTTCTCAAATCGCCCTTTAGTACCATTTCTTTCATTACTAGTGCATCTATTTTTAATTCATGCATCGCTTCAATGGATTTCATATTTTTACCAGTTGTGTTTTTCACTTGTTCATCAATAATTTTTGCAGATTCTCTTGATGCGCCCGTGTAATACAATACCAATGAGTTTTCTAATTCGTTAACGATCCAACTTTTAACTCGTAATGGATTTACTATGACTCTATCATCGTTATAAAACTCTATAAAATTAATCCCACCAAAAGTTGCAGCGTATTGATCTTGTTTCCCACCACTAAGTCCAACATCTTGCCTCTCGATCTGATAAGCTAACTGAGCAACATCATATTCTCCCAGTGGGAGATTCAACCATTCTGCAAAGGCATGTAATATAGCCACAACCATCGTTGAGGAAGAACCCAACCCCGATCCCGCAGGTGCATCAGAATACGTTGTCATCCGGAAAGATAATGGTACAGATTGATGATATTGCTTAATTATTCGATTGTATATTCCTTTATGCAAATCCAATACACCATCAAACTCCAAGAAATATGTAGAATCATACTCTGTATACTCTTCTCGATCAGTTGCATAAAAGCTTATTTTATTATCACTTGTCGGTTCAATCGTACAATAGGCATACATATCTATAGTTGCATTTAGGACATATCCCCCAAATTCATCGCAGTATGGTGAAACATCTGTCCCACCACCTGCTAGTCCCAACCGTAAAGGAGCTTTTGAACGAATTAACATACTAGCATTCCCCTATCTTGTCAAAAAATTCTGTCCCATTTTGATTCTATCTCTCCAATAATTCAACAAATCTTCCATCGTTGTCTCAAATGGAATTTCAGGAGCCCATCCCGTATGATTCTTAAACTTGCTTGTGTTGGGTACTTGGAGATCCGCATCAATCGGTCTAATTCTTTCTGGATCCGTTTCAATTTTAATATCTTTCACACTTGACATACTGACAAGCGTATTTAACATATCACGCACTGAGCAAGTGTAAGTTCCTCCAATATTATAGTATTCCCCTGCTATTGGATTTACGGTTACTAACATGTAATAAGCTCTTACAGCATCCCTTACATCAGCCCATGTTCGTAAAGAATCTAAATTGCCCGTTTTAACAATTGGAGGAATCATCCCCGCTTCAATCATCGCAATTTGCTTTGCAAAAGTCGATTCAGCAAACACATCTCCTCTGCGAGGACCTGTATGAGTGAACATCCGAGTTGTCATTACTTTTTGACCATATGCCTCAGCATGATATCGACCAATAAGATCAGTACCTATTTTGGAGATTGCATACGGTGATGCAGGATGAAAGGAACATTCTTCATCTATAGGCAACTTTTCTTTTGGAACTCTCCCGAACACTTCAGACGACGCGCACACATGAATCACAGGATCAATGTCATTAAATTTCCGAAGAGCCTCAAGTAATCTAGCTGTTCCCAATATATTCACGTTAAAAGTATCGATTGGGGCATCAAAGCTTGTTTTAGGAAAACTTTGAGCGGCAAGATGAAAGACATAATCAGGTTTGCTTTTTTCGATAACCTCATGCAACGACAAATAATCATTTAAATCTCCATATAAAATATGGACTCGATCTCTCTGATTAATTCTCGGCAAAAGATGTTGCACATTGTCAAACGGGCTTCTCCACCGACACATCCCATATACTTCCCAGTCTGTATTCTCCAATAGATAATCTACTAAATGAGAACCAACCATTCCTGTAATCCCTGTAATTAATGCTCGCTTTTTGCTCATACAAAACCATTCCCCTTCTATACATATAATTAAGAAAACTCTCTACTCATTGCTTCATCAATCTTAATTGGCTTTCTTTTTAGTAGCTTTTCAAAAAAGATCGAGGCCATATCTATCGTTTTAGGTCGAGCTTTAAAAAATGATTCATCTGGTTCAGTCGTACGATATTCAAGTTCATTATTCACATTGAATTTATAAAACTGCACTAAATCCACTCTAGATAGTAAGCTAGGACCGCAAATATTAAAGATCTGATTACTCCATTCATCCCAATCTTGCTCAATAGTAATAATAGCTTGTATTAAATCTTCAATATATACAGTTCGTCTAAATATAGGATGAAATACATCAACAACCTCGCCTTTACGACAACAACCATGGATATAACTTGTAAATTTATCTTCTCTAGAGAAAATATAAGATAATCTAAAAACTTTAAAGTTTGAATAACCCATAAATTTCTGTTCGATTTCCTGCTTCATTAATGCATAATTCCCAATCGGGTTAGTATCAGTATTTTCATCCACCTCAGATTGTTGAAGACCGTACACCGTATCAGAAGACATAAATAATACTCTCGCATTCCTCTCAATACATTTAGATATGAAATAAGCAGTCCCGCTAACGTTAATTTCATATGCCGTATCATAATCACGATTACATATGTCTGGAGAAGAAATAGCAGCTAATAGCACGATAAAATCATTCTCTTTAATCATGCTATAATCAAACGATTGTGGTTCTAACAAGTTTAAATACATAGCTTGTTCTTCAGTATGACTAGATGTTACATTTATGTCTTGATTATCTATAGGATTTGAATCTAAATAGTCTATCAATCTTTTTGCAATATAGCCACTCTTTCCGATAATAAATATACTCAT

Protein sequences of DBSCAN-SWA_3

>NZ_CP045293|4914172:4931045|4927515_4928103_-|WP_152395470.1|DBSCAN-SWA
MQSFINNQIKESYEIKRLILESTELTKLIKEVAEKTTVVYRNGKKTLLAGNGGSAADAQHIAGEFVSRFYFDRPGIPSVALTTDTSILTAIGNDYGYERLFARQIQAQGSEGDLFIGISTSGNSPNIISALKECREKGIITVGLTGASGGRMEEFCDYCIKVPSDETPRIQESHILIGHIICAVVEESIFGKGFN
>NZ_CP045293|4914172:4931045|4920654_4921719_-|WP_152395464.1|DBSCAN-SWA
MINTNFWVNKRVFITGHTGFKGSWLSLWLHSMGAKVYGYAQIPNTEPSLYHVCGIDEILEKSFIADIRDSKSLQEAMEFSSPEIVIHMAAQPLVRESYINPVDTYSINVMGTVNLFEAVRNCSSVKAVVNVTTDKCYENKEWVWGYRENEPMGGYDPYSSSKACSELVTSAYKNSFFYHNEKRFVGVASARAGNVIGGGDWAKDRLIPDCIKALMADQTIIIRNPYSIRPWQHVLEPLGGYLLLAEKLFEDGEKYSEAWNFGPYDIDAKPVEWIVQEMCNKWGTEANYRVDSNPQPHEAQYLKLDCSKANAILNWSPRWNLETAIEKIVSWTKAYRNNENMREVCIKHIKEYQS
>NZ_CP045293|4914172:4931045|4918865_4920635_-|WP_152395463.1|DBSCAN-SWA
MKLSDYVIDFIKKEGVSHVFEFIGGAIAHLLDSIAKRDDIECVSVRHEQAASFAAEAYARMNGKLGVAMATSGPGALNLLTGIGSCFFDSVPCLFVTGQVNTYEYKFDRPVRQIGFQETDIVSVVTPLTKYAALVTDPSQIRYSLEKAVYLAQNGRPGPVLIDIPMNVQRADIDPSNLESFFDSDEYKELSMANDVLDARIISQLYEMISNAQRPVILAGGGVRVSNAYEELSLFIEKTGIPVVSSLMGLDVISHDNPLYCGLIGSYGNRYSNMTLANCDLLIILGSRLDSRQTGTRPDTFARAAKKIHVDIDPNELNCKVQVDIAIKTDLLQFLKQMNIKLKNYRKPDLSDWLMKIETLKAKYPTSSGITSADIIEPNQFMGVLSSYARKIKAICLDVGQHQMWASQSFKLQDGQRILNSGGMGAMGFALPAAIGATLATNQESLVIAGDGGIQLNIQELDTLRRMNLPVKICVMNNNCLGMVRQFQDLYFDGRQQSTVSENPNFGDIFEAYGIPSYQVRSLSETATIEQFFAEEGPAFIEVMLQKNTEVQPKLVVNRPIEDMSPHLDREELKEVMLIDLVEEMEVPK
>NZ_CP045293|4914172:4931045|4922540_4924151_-|WP_152395466.1|DBSCAN-SWA
MLIIDAEEYLKYLKECRHLKQGSIVKFKNTGEYGLIGYELENIFQVFKLSKNAPEIQNGNFHEVIKVNKETPLFLDVRDKLHVLKNDIEFIFDLSEHDFEKVMRLEILSKVENYYDLFHSNRNKKFDVEKSSLSYGGRIYDEKEMRSLVDSSLDFWLTAGRYNKQFEKEFAEFLGVRYALLTNSGSSANLLAFSTLTSPKLGDRRVMPGDEVITVAAGFPTTVAPIIQNGAIPVFIDVELGTYNIMVDRIEDAITPRTKAIMVAHTMGNPFELDKVMEIAEKYNLWVIEDNCDALGSTFNGKLTGTHGHIGTSSFYPPHHMTMGEGGAVYTNDPKLKMIIESFRDWGRDCWCESGCDNTCKKRFGWELGSLPYGYDHKYTYSHIGYNLRVTDMQAAIGVEQLKKVPSFVQARKNNFNRLLAGLRELDQYFILPRATENSDPSWFGFILTLRDGVNFTKNEIVDYLEANRIQTRMLFAGNLIRQPAYQNVNFRIHGGLKNTDKILYDTFLVGVYPGLSDEMIDYVIDKIKEFVYSKN
>NZ_CP045293|4914172:4931045|4915204_4915753_-|WP_152395458.1|DBSCAN-SWA
MNIIDTKLQGVRIIEPAVHGDHRGFFMESYNSAKFREYNMDYLFVQDNHSLSVEKGVLRGLHYQLNPKAQTKLVRVAAGAIYDVVVDIRRNSPTFGQWVGVHLSAENKRQLLVPQGFAHGFCTTEANTEVLYKVDALYSPEHDRGILWNDPALGIDWPVEQPILSDKDTKHPVLRDADINFD
>NZ_CP045293|4914172:4931045|4916547_4916919_-|WP_152395460.1|DBSCAN-SWA
MDNQFVKFIIVGVINTIFGYSVFSLFIFVGLHYTLASLLSTLVGILFNFKTTGRIVFKSSDNSLIIKFFITYGVTYLLNLALLTFLKEFVSIYIAYAILILPMSMVSYILNKRFVFRVKATNN
>NZ_CP045293|4914172:4931045|4929144_4930161_-|WP_152395472.1|DBSCAN-SWA
MSKKRALITGITGMVGSHLVDYLLENTDWEVYGMCRWRSPFDNVQHLLPRINQRDRVHILYGDLNDYLSLHEVIEKSKPDYVFHLAAQSFPKTSFDAPIDTFNVNILGTARLLEALRKFNDIDPVIHVCASSEVFGRVPKEKLPIDEECSFHPASPYAISKIGTDLIGRYHAEAYGQKVMTTRMFTHTGPRRGDVFAESTFAKQIAMIEAGMIPPIVKTGNLDSLRTWADVRDAVRAYYMLVTVNPIAGEYYNIGGTYTCSVRDMLNTLVSMSSVKDIKIETDPERIRPIDADLQVPNTSKFKNHTGWAPEIPFETTMEDLLNYWRDRIKMGQNFLTR
>NZ_CP045293|4914172:4931045|4921715_4922510_-|WP_152395465.1|DBSCAN-SWA
MKVVILAGGYGTRISEESHLKPKPMIEIGQKPILWHIMKLYSQHGFNDFVICLGYKGFYIKEYFAHYFLHESDVTFDFRNDNQIITHNHSAEPWKVTLVNTGLDTMTGGRVKRIQPYIEDEPFMLTYGDGVSDVNITELVNYHKLHGRIGTVTSVQPSGRFGALNITENNLVKGFQEKPKGDNSWINAGFFVLQPEIFNYIADDSTIFEKAPLETLAKNEELMSYKHDGFWQPMDTLRDKNYLEDLWGSGKAPWKTWDRDPVNV
>NZ_CP045293|4914172:4931045|4917909_4918854_-|WP_152395462.1|DBSCAN-SWA
MVVIKKKIAVLGATGHIAKNIITGLCLKKEHEIFAYARTEAKLVEFLEAERLEVVTILDLNDFKERFFDVIINCVGIGNPQDLQQDPYKIFHLTESFDNLIIEKIRDSQETLYINFSSGAAYGEDFMKPVEYTTSNKVKINSFSTKDYYGVTKLYTEAKHRSLLMNNIVDLRVFGFFSRYIDLNSKFLMTDIINCIRTGNELVTSPSNIIRDYIHPHDLNQLIERLINNPEVNDAFDVYSKCPISKFDLLNYFKDNHQLSYRIIEGDVKSSVTGNKDNYYSEFHKAQNVGFHPQYSSIESIDDEYKYIRMRLEK
>NZ_CP045293|4914172:4931045|4915765_4916509_-|WP_152395459.1|DBSCAN-SWA
MKGIILAGGTGSRLYPLTKVTNKHLLPVGKYPMIFHSVNKLMQADINDILVVTGKEHMGDVVNLLGSGRDMGVTFTYKVQDEAGGIAQALDLAEQFVGDDQMVVILGDNVFEDDISGYVANFREQQTGAKILLQQVHDPQRYGVAELNGDNIVSIEEKPRAPKSNYAVTGIYMFDSTVFDIVKTLKPSGRGELEITDVNNAYIARGELTYDVLQGWWTDAGTHVSWAKANELAQNITFSEEFGKLKL
>NZ_CP045293|4914172:4931045|4914172_4915192_-|WP_152395457.1|DBSCAN-SWA
MKLLVTGGAGFIGSNFVIYMVNKYPEYQIINLDALTYAGNLENLTSVQDKPNYTFIKGDIADAVKVEEIFQQHQIDVVVNFAAESHVDRSILDPGIFVQTNVMGTQVLLDAARKYNVNKYVQISTDEVYGTLGDTGLFSETTPLAPNSPYSASKTGGDLLVRAYHETYGMNVNITRCSNNYGPYHFPEKLIPLMISNALNDKQLPVYGDGLNVRDWLYVEDHCSAIDLVIHKGVSGEVYNVGGNNERTNIQIVETILEALGKPKSLITYVADRLGHDRRYAIDATKIRAKLGWQPQYPFEKGIQKTIQWYLDNKGWWTRIQSGAYQEYYAKQYGERLGE
>NZ_CP045293|4914172:4931045|4926818_4927514_-|WP_152395469.1|DBSCAN-SWA
MEAIILAGGFGTRLQSAVNDVPKPMAPINGQPFLTYLLKYLLKYDIRSVLLSTGYKHEVIEDYYGSCFQGVMRLEYSVEKEPLGTGGAIAQSMRYTTEEDIIVINGDTFFNVDLKEMMLFHRTQAGEMTMALKPMSDFERYGKVDHVNNRVVKFQEKQYTSFGDINGGVYILNRSIFNGCNLEKTFSFETDFLQKHLQRIQVNSYIADEYFIDIGIPEDYYKAQSELIKFE
>NZ_CP045293|4914172:4931045|4926337_4926826_-|WP_152395468.1|DBSCAN-SWA
MNKAVFFDRDGVINVEKNYVYKIEDFEFVDGIFDVMKHFQSLGYLLIVITNQAGIGRGYYSEEDFHKLNDWMIERFKVEGIEITKVYYSPYHPEHGIGEYKKDSWCRKPNPGMILQAKDDFDIDLRESILFGDKDSDIEAGIRAEVGENVLVQMNVKINANK
>NZ_CP045293|4914172:4931045|4928103_4929132_-|WP_152395471.1|DBSCAN-SWA
MLIRSKAPLRLGLAGGGTDVSPYCDEFGGYVLNATIDMYAYCTIEPTSDNKISFYATDREEYTEYDSTYFLEFDGVLDLHKGIYNRIIKQYHQSVPLSFRMTTYSDAPAGSGLGSSSTMVVAILHAFAEWLNLPLGEYDVAQLAYQIERQDVGLSGGKQDQYAATFGGINFIEFYNDDRVIVNPLRVKSWIVNELENSLVLYYTGASRESAKIIDEQVKNTTGKNMKSIEAMHELKIDALVMKEMVLKGDLRTFANYLGKSWEAKKRTASTITNQSIDRVYDIAIASGAYAGKVSGAGGGGFMMFMVDPAKRINLIKELQRLDGVVMNFHFTKNGAESWRIN
>NZ_CP045293|4914172:4931045|4924292_4925657_-|WP_152395467.1|DBSCAN-SWA
MHFHLIHEKKKKKKIIAFGLIVSPIIFYLMFKKLFLKSSILVGTGYTSIKINVYSVIKFFIGGLLNLFGFNIGPEHLNGIPINQVNLTTIIVSVLVLILSMIVFIAAIKGKDKKEKLIEFKIFLIMLMLVCALVLVSSITVYQELRWLQTPYLVFIIYMGYLFAKINSKKLMMILMILFTCCNLKQNSYYKDYIHNIYFVYSQQISDSAYDETIKKYGTNIRQYKVFIEKHRDIDWPLLDSLFLKPYLGDDTFKVEYVDNILDVDLTKIDPTKVVLLKLNDSQKRFINVTNEVILYKNKALGKNKNIKYSLIDHFHEGEVTPQSVNEDTPNGEGVFIFDWTTQFQKINTLTIISGFKYTYKNIFIPTDSKICGDLILPLKGSDGANFYISINDNGNERRIYESNVTQESNFNEIEISIEGYSGKNVDITFGVESPNGNNIADWIALGDLGIAQR
>NZ_CP045293|4914172:4931045|4916944_4917913_-|WP_152395461.1|DBSCAN-SWA
MKKISIVTPCYNEEDNVEELYQRVREVFDELSGYVYEHIFIDNASKDNTVAILKRIALKDQNVKIIVNARNFGHIRSPYHALLQADGDAVILLVADLQDPPNMIIDFIEKWEEGYKVVLGVKTESHESAAMFAIRKMYYNFINRVSEIELTKNNTGFGLYDRKIIQILREINDPYPYFRGLISDIGFESYKIEYVQPVRKRGITKNNFYTLYDMAMLGITNHSKIPLRLAAMLGFLMSAVSLLVAVGYLIAKLVFWNYFTLGLAPLVIGLFLFSSVQLFFIGIIGEYIGSIHTQVLKRPLVVEKERINFETIINQELERVKG
>NZ_CP045293|4914172:4931045|4930190_4931045_-|WP_152395473.1|DBSCAN-SWA
MSIFIIGKSGYIAKRLIDYLDSNPIDNQDINVTSSHTEEQAMYLNLLEPQSFDYSMIKENDFIVLLAAISSPDICNRDYDTAYEINVSGTAYFISKCIERNARVLFMSSDTVYGLQQSEVDENTDTNPIGNYALMKQEIEQKFMGYSNFKVFRLSYIFSREDKFTSYIHGCCRKGEVVDVFHPIFRRTVYIEDLIQAIITIEQDWDEWSNQIFNICGPSLLSRVDLVQFYKFNVNNELEYRTTEPDESFFKARPKTIDMASIFFEKLLKRKPIKIDEAMSREFS

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_152395457.1|4914172_4915192_-	dTDP-glucose 4,6-dehydratase	I7HTA3	Enterobacteria_phage	2.4e-76	46.5
WP_152395458.1|4915204_4915753_-	dTDP-4-dehydrorhamnose 3,5-epimerase	I7HJC4	Enterobacteria_phage	3.3e-40	47.5
WP_152395459.1|4915765_4916509_-	NTP transferase domain-containing protein	I7I009	Enterobacteria_phage	1.8e-52	44.0
WP_152395460.1|4916547_4916919_-	GtrA family protein	NA	NA	NA	NA
WP_152395461.1|4916944_4917913_-	glycosyltransferase	U5P087	Shigella_phage	7.7e-40	33.8
WP_152395462.1|4917909_4918854_-	NAD-dependent epimerase/dehydratase family protein	NA	NA	NA	NA
WP_152395463.1|4918865_4920635_-	thiamine pyrophosphate-binding protein	A0A0P0CDR3	Ostreococcus_lucimarinus_virus	3.1e-87	33.8
WP_152395464.1|4920654_4921719_-	CDP-glucose 4,6-dehydratase	D6PH86	uncultured_phage	4.5e-09	22.4
WP_152395465.1|4921715_4922510_-	glucose-1-phosphate cytidylyltransferase	NA	NA	NA	NA
WP_152395466.1|4922540_4924151_-	lipopolysaccharide biosynthesis protein RfbH	A0A218MN59	uncultured_virus	5.2e-65	33.8
WP_152395467.1|4924292_4925657_-	hypothetical protein	NA	NA	NA	NA
WP_152395468.1|4926337_4926826_-	D-glycero-beta-D-manno-heptose 1,7-bisphosphate 7-phosphatase	NA	NA	NA	NA
WP_152395469.1|4926818_4927514_-	NTP transferase domain-containing protein	A0A0G2Y8M0	Acanthamoeba_polyphaga_mimivirus	9.5e-08	26.3
WP_152395470.1|4927515_4928103_-	SIS domain-containing protein	A0A067XQR2	Caulobacter_phage	3.2e-12	32.8
WP_152395471.1|4928103_4929132_-	dehydrogenase	A0A222YW25	Synechococcus_phage	1.9e-65	43.0
WP_152395472.1|4929144_4930161_-	NAD-dependent epimerase/dehydratase family protein	A0A222YY99	Synechococcus_phage	2.3e-103	54.3
WP_152395473.1|4930190_4931045_-	NAD-dependent epimerase/dehydratase family protein	A0A222YYW2	Synechococcus_phage	4.4e-39	33.3

Sequences of DBSCAN-SWA_4

Nucleotide sequences of DBSCAN-SWA_4

>NZ_CP045293|6309164:6324370|DBSCAN-SWA
AATGAAGACATTAGTATTGGCTGAAAAACCCTCCGTCGCGAGGGAAATTGCAAGAGTCATGGGGAGCAACCAGAAGCACAAGAGCTATTTCGAAGGCCCGAAGTATATCGTTACCTGGGCGCTTGGGCATTTGGTCGGTCTGGCAGAGCCGGAAGACTATGACGTGAAGTACCGGACATGGGAGTTGGAGCATCTGCCAATCATGCCGGAGAAGATGAAGCTGAAGGTGCTGCGTGAGACATCGCATCAATTCAAGGCAGTGCAGCAGCTGGCAGGCCGTCAGGATGTGGCGGATCTTATCATCGCAACGGATGCGGCGCGTGAAGGGGAGCTCCTCGCACGCTGGATTATGGCGATGGTGAAGTGGAAGAAGCCGTTCCATCGGCTGTGGATCTCTTCACAGACGGACAAGGCGATCCGCGAAGGATTTGCGAATTTGAAGCCTGGCTCGCAGTACAACCGGCTGTATGAGTCGGCTCGCTGCCGTGCGGAGGCGGATTGGCTCATTGGACTTAATGTGACGCGTGCGCTCACTTGTAAATTCAATGCACAATTGTCGGCTGGCCGTGTGCAGACGCCAACGCTAGGGATGATTATGGATCGCGAGAACGAGATTCGTAATTTCCGTTCCGCAGAGTATCAGACGCTTCAAGGGGAGTTCGAAGGATTCCAGGCACAGTGGCGGCCTCGAGGCGGTCAAGGGGATGGCCGGATGTTCGATCCGAATCAAGCGGAAGCGCTGCGTAAGAAGGTGGACGGCAAGAAAGGCAAGGTCACCTTGGTGAAAAAATCCGAGAAATCGGAGCCGCATCCGCTCGCGTATGACTTGACTGAATTACAGCGGGATGCGAATAAACGGTATGGGTTCTCTGCTAAGCAGACGTCGAACGTGCTTCAGCGACTGTACGAGCAGCATAAGCTCGTCACGTATCCACGTACGGATTCTCGCTATCTGTCCAGCGATATGACGGACACGCTGCCAGAGCGCATCCGGTCCGTAGCTGTTGGACCGTATGCCGCCATCGCCAAACCGCTCTTGCGCGGCAAGCTGCCAATCACGCGCCGTGTTGTTGATGATTCGAAGGTCTCGGATCACCATGCGATTATTCCGACGGATCAGACCGTTCTGCTGAATGCGTTATCGAATGAAGAGCGGAAGCTCTATGATCTGATCGTGAGACGGTTCTTGGCATTATTCTATCCAGCAGCGAAATACGAGTTAACGGCCTTAACGATTGAGGTCGAAGGCGAGACGTTCATGACACGCGGCAAGACGGTCATCCAGAACGGTTGGCGTGAAGTGTACGGGCAAGAGGATAGCTGGGACGATGACGAGGACGAGTCTGGTGCAGATCGCGACGACGACCGATCCGGCATTCAGCTGCTGCCAAGCTTGCGTGAAGGGGAAGCTGTTCAAATGAAGCGGGCTAACCTTCGCAAAGATCGCACGCAGCCTCCGAAGCGGTATACCGAAGCATCGCTACTCGGTCAGATGGAGAAATACGGTCTCGGCACACCGGCGACGCGCGCGGATATTATCGAGAAACTCGTGTCGAGCGATACGATCGAGCGGCAAGGGGCTTCCTTACATCCAACGGGTAAAGGCGTTCAGTTGATTGAGCTTGTGGCAAGCGAACTGCGGACACCGGAGTTAACAGCGAAATGGGAACAGGAGCTTGAGAAAATTGCACGCGGTCAAGGCGGGACAGAACCTTTCATGAAAGGGATTCGCGACATGGCTCAGAGCCTCGTCAGCGGTGTGAAGACAAGCGATGCTGCGTATAAACCGCATAACTTGCTGAACAGCCGTTGCCCAGAGTGCGGCGAGAAGATGATGGAGAAGAAGGGCAAGCGCGGTAAAATGCTCGTCTGCTCCAGCGGGGATTGCAGCTACCGTCGATCCGGCGAGAAGCAGCTCTCCAACAGACGCTGTCCGCAATGCCATAAGAAGATGGAGCTCAAAGACGGGAAGGCTGGCAAGTATGTGCAATGCCTCGGCTGTAATGTCATCGAAGTGCTGGATGGGGAACGCGGCGGCCGTGTGAATAAGCGAGAGCAGCAGAAGCTTGTGAAGCAATTCGAGAAGACAGAGTCGATGGGTTCGAGTCTCGGTGACGCACTGCGGGCAGCGCTTGAGCGAAAAGAGTGAATTATCTGAAAAGTGAATTGTCAGAAAATACGAACTTTAATTTAATGTAAACAATTTAATGTTCGTCTTTAAGTTGACATCTCATGTAATGGACTGATAATATAGGGATATAAAGTGGCGAGCCACGAATAAATGATCTCGTATAATTGTGGGGATATGGCCCAAAGTTTCTACCCAAAGACCTTAAATTTTTGGACTACGAGTGAAAGCCTAGCATCTGGCGAGGACAGCGATGATCCGTGGGTTACTGCTGTCGAAATTTACTGTCGAATATCGCATCATAAGGCCTGCGTTAGGCACAATGCTTGCGAATCTGCAGTGATGCGAGTGTGCAAGACTCTTTCATTTTCTTATTCCTAAAAAAACGGTCCGAAGATAGAACGAAGTGTATGCTTGGCGTACACGCCTATCCGAGGACCTTTTCTTATATTTATTCCATTACTGAATCGATAGAAAGTGGGTTATGACATGTCAGTACAAGTAGGCGTCATTATGGGCAGTCAGTCCGATTGGGAGACAATGAAACATGCATGCGACGTGCTGGATGAGCTAGGGATCGCATATGAGAAGAAGGTCGTATCGGCTCACCGTACACCAGACCTGATGTTCCAATATGCAGAGAGCGCGGTAGAGCGAGGCTTAAAAGTCATTATTGCTGGCGCAGGCGGCGCAGCGCACCTCCCAGGTATGGTGGCAGCGAAGACGATTCTTCCAGTGATCGGAGTGCCCGTGAAGTCGTCTACACTGAATGGTCTGGATTCCCTTCTATCGATTGTACAAATGCCAGGGGGCGTTCCAGTTGCTACGGTAGCGATTGGAAATGCAGGAGCAACGAATGCAGGACTGCTCGCAGCCCAAATCATCGGCGCATTCGATCCAGCGGTACAGCGGCGTGTGCAGTCACGACGCGATGCCATTCGCGATCATGTGCTTGAAGGCAGTGATTCACTATGATCGAGAAGAACATGATTACATCGGTTGAGAGAATCATCGCTCCAGGCTCGACCATTGGTGTACTAGGCGGCGGACAATTAGGCCGGATGATGGCGTTATCGGGCAGTAACCTCGGTTATCGCTTCGTGACGCTCGATCCGATGCCGGATGGCCCTTGCGGTCAGGTCGCAGAGCAGATTATCGCTGCTTATGATGATCAGGATGCAGCTCGGAAGCTCGCGGACGAAGCGGATGTCATTACGTATGAGTTCGAAAATGTGGATGCCGGCGTGGCGGCGATGCTGATGTCGGAATCCTATGTTCCACAGGGCAGTGAGCTGCTCTACACGACGCAGCATCGACTGCGGGAGAAGCGGGCGATTGAAGCGGCTGGCGTGCGCGTCGCGCCTTACGCGGAGATTACGAGCGAGGAGGACCTTCGCGCTGCGGTGGATCGCTTTGGATTGCCTTGTGTATTGAAGACGGCTACTGGCGGATATGATGGCAAAGGGCAATGGGTCATCCGTTCAGCGGATGAAATCCCAGAGGCTTATGCAACGCTTGCAGCGGCGAAGACAGAGCTCGTGCTCGAACAATTTATCCGGTTTACAAAGGAATTGTCAGTCATTGCAGCTCGTAGCCCACGAGGAGAGGTTAAAGTATTCCCTGTAGCAGAGAATATTCATGTGGACAACATTCTGCATCAATCCATTGTTCCAGCTCGGGTATCGTTCGATATACAGGATAGAGCAGAAGCGCTAGCGATTCGCATTGCGGAATCGATGAATGTCGTCGGGTTGATCGCGGTAGAGCTCTTCTTAACGGAAGACGGTGAATTATTCGTCAATGAATTAGCACCAAGACCACATAATTCTGGGCATTATACGATGGAGGCCTGTCGAACGTCACAGTTCGAGCAGCATGTGCGGGCCATTTGTAATTTACCTCTTGGAGATACGATGTTGTTGACGCCCGTCGTCATGGTCAACGTGCTAGGAGAGCATGTTGAACCGCTGCTTGCCCATATGGTGCAGGAAGATGAAGCGGCTGAGGCGTTCAACGTCGCTCCGAAAGTTCACTTATACGGCAAAAAAGAAGCAAAAGTAAAACGAAAAATGGGCCATGTGAATGTCTTGGCAGATCATCTAGATGATGCCCTCGCATGGATCGAGAAAACACAAATTTGGAGGAATCATTAGATGTTAGAACGTTACAGCAGACCGGAAATGAGAGCAATTTGGACGGAAGAGAATAAATTCAATTCCTGGTTAGAAGTTGAGATCTGTGCGTGTGAAGCGTGGGCAGAGCTAGGCGTCATCCCGAAAGAAGATGTTGCGACGCTCCGTAAGAACGCAAGCTTCAACATTGACCGGATTTATGAAATCGAGCAGGAGACACGTCACGACGTGATCGCGTTCACGCGCGCGGTATCTGAGTCTCTAGGCGAAGAGCGCAAATGGGTGCATTACGGATTAACGTCGACAGACGTCGTGGATACAGCACTTGGTTATGTATTGCGTCAAGCGAATGAAATTATTGAGAAGGACATTCTTCAGTTCATCGACATTCTGAAGACGAAAGCTCTCACTTACAAACATACGCCGATGATGGGTCGTACTCACGGTGTGCATGCGGAGCCGACAACATTCGGACTCAAAATGGCGCTCTGGTACGAAGAAATGAAGCGCAACTTGGAGCGCTTCCGCCATGCAGCGAACGGTGTACAGTATGGTAAAATCTCCGGTGCAGTCGGCACATACGCGAATATCGATCCGTTCGTTGAGAAGTTCGTGTGCGAGAAATTAGGAACAACGGCAGCGCCGATCTCGACGCAAACGCTGCAGCGTGACCGTCATGCCGAATATATGGCGACACTTGCGTTGATCGCAACGAGCTTGGATAAATTCGCGACAGAAATTCGTGCTTTGCAGAAGAGTGAAGTGCGTGAAGTGGAAGAGGCTTTTGCGAAAGGTCAAAAAGGATCATCAGCAATGCCGCACAAACGCAATCCAATCGGTTGCGAAAATATTTCCGGTCTTGCGCGCGTCATCCGCGGCTTCATGGTATCGGCTTATGAGAACGTACCGCTCTGGCATGAACGCGACATTTCGCACTCCTCCGTTGAGCGTGTGATTCTGCCGGATGCGACGATGCTGCTCAACTACATGTTGAACCGCTTCGGGAACATCGTGAAGAACTTGACGGTGATGCCAGAGAACATGAAGCGCAATATGGAAAGAACATTCGGCGTACCGTTCTCAGGCCGCGTGATGACGAAGCTGATCGACAAAGGCATGAGCCGTGAGCAAGCGTACGATACGGTTCAACCGCGCGCGATGCAAGCATGGGAAGAGCAACGCAGCTTCCGTGAGATTATTGAAGCAACACCTGAAATTGCAACGGTATTAAGCGCTGAAGAGATTGCGGATGCATTCAACCCGGCTTGGCATTTGAAGCATGTGGATACGATTTTTGCGCAATTAGGATTGGAATAGTAGAGGGAGAAGGGGAGGAATAAGGTGTCTGTCAGAGCGATTTCGACTGCTGTTGATCTAGTGAAAGCGCCGCTGCTCTATAAAGGGAAAGTGCGCGAGTTGTATGATCTTGGGGAACATTATTTAATCGTCGTGACCGACCGTATTTCCGCTTTTGATTATGTGCTGGAGCCGGCGGTACCGGAGAAGGGCAATGTACTGAATCGCCTCACGGCATTCTGGTTCGAACAGACGGCGGCGATCGAGCCGAACCATGTCGTTCATACCGATGTCGAGAAGCTTGGCGATCTGGTGACGGAACCAGAATTGTTGAAGGACCGCATCATGGTAACGAAAAAAGCAGAGCGCATCGATATCGAATGCGTGGTCCGCGGCTATATTACAGGCGGCGGATGGCGACAGTATCAGCAATCCGGTTCGGTGAACGGGATTGCGTTACCAGCTGGCATGAAGAAGAACGAGCGCTTCGCAGCGCCAATCTTCACCCCGGCGGCGAAAAATGATGTGGGGCATGACGAGGACATCTCCTTCGATCGGATGAAGGAACTCGTCGGCGAAGAGCTTGCGCATGAACTGCAAATGAAGAGCCTTCAGCTCTACAGCTTCGCACATGCTTACTGCGAGAAGCGCGGGATCATCCTTGCGGACTGCAAGTTCGAGTTCGGCTTGATCGACGGCCAAGTCATTCTGATCGATGAATTATTCACCCCGGATTCCGCTCGGTTCTGGGTGAAAGAAAATTATGCATTGAACATCGAGATTGACAGCATGGATAAAGAGCCTGTGCGCACGTATTTGGCGAACAGCGATTGGGATAAGAACAGCGTGCCGGATCCGTTGCCAGCCGAAGTAGTGGCGGAGACGACGCATCGGTACCAAGATATCTATCGGAGATTGACGGAGTAGTCGCGAGGCGTGGCGATGATGCTGGACATAGGGGGGCGGAACGCAGGTGTATCGTCTTCCATCGCTGTTGAAATCGGGAAAGGTTTGATTGGATGTTATGGTATTTTCCCGATTTCAAAGGCGAGCGCTATCGCTCTCCAGCCGCTACACCCGCTTTTCCTTCCTGAGTCCAGCATCATCGCAGCTTGCCCCTCCCCATCACGGGGAGGGGGCAGGGATGCACCGTTCAGCCATAGGCAAGAACGGTGTCGTGAACAACGCTGAGAGCGAGTGCGCCGAGAATCGGCCGCACGGCAAGCGAGAAGCGCTGGGAGCAGTTGTTCAGGCATAGCCTGAAATAGCCCCGCGTCTAGCGAAAAAGGTAGTAGGGTTTAGGTGTTATAGCCGCAGTAGAGCGTGTGCGACGGGGTTGCCTAGCACAACCCCACGCACAGTAGCGCTCCTAGCACACTGTGACGCTCGAGGCACGTACTCACGCATCTCCACCGATAGATTTGAAGTTACTAGATTCGCACGCATGGCAAGCGTATGTGGGACGATGTTTCGGCCGTGCTAGAGAGCACGATCGAAACATCGTCCCACATGGGAGCGATCATTGCACACAAGTAGATAGATTCCGCCGCAGTCCGTCATCAGGCCGATTTCGGGGTCCAGGGGCGTAGCCTCTGGGGTCCCCTTTCCAGATGGAAGGGGGATTTAGGGGGATGGTAAAAAGGTTTTATCAAAGAGGGCCCCTGCCCAAAAAGGGAATAAACAATCTCCATTTTTATATTATTTTTCACTCTAGGAGGAAATAATCGATGTTCAAAGCAACCGTGTATGTCACTGTGAAGGAAAACGTATTGGATCCACAAGGTGTAGCCGTTCAAGGCGCATTGCATTCGATGGGATTCAGCGAAGTTAGCAAGGTTCGAATCGGGAAGTATATGGCGTTTGAAGTCGATACGACAGATCGCGCAGAAGCGGAAGAGCGCGTACGTCAAATGTGCGAGAAATTGCTGGCGAATACGGTGGTTGAAGACTATCGCTTTGAGTTGGAGGGTTAATAGCATGAATTTTGCAGTTATCGTATTTCCAGGTTCCAACTGCGATATCGACTGCTACAAAGCCGTAGAACAAACGGTGGGGCAGCCAGTCGATTACGTATGGCATACCGCGACGGACTTATCCAAATATGATTGCATCTTGATTCCGGGTGGCTTCTCCTACGGTGACTACCTTCGCAGCGGCGCGATTGCACGTTTCGCACCTGTTATGACTGAAGTAGCGAAAGCAGCGGCAGCTGGCAAATATGTAATGGGTATCTGCAACGGCTTCCAAGTGCTCACAGAAGCGGGACTGCTGCCAGGCGCACTTCGCCGGAACGTGTCTCTGAAATTCCGCTGCCATTCGACGATCTTGCGTGTGGAGAACAACCAGACAGCATTCACGAATCAATATGAAGTTGGCGAGTTGATCGATATTCCGATTGCGCACGGGGAAGGCAACTATTATTGCGATGAAGCAACGCTAGAACAACTGAAGAAGAATAACCAGATTATTTTCCGCTATTCGGATAATCCGAACGGCTCCTTGGAGGATATCGCAGGAATTTGTAACGAGCAGGGCAATGTCCTGGGTCTTATGCCGCATCCAGAGCGCGCAGTGAACCAACTGTTAGGCTCGGAAGACGGTAAGAAAATGTTTACATCGATTTTGAATGCATGGAGGGAACAACATGACGCAGCAAGTATCGGCTAAGGAGCCAACAGCACAGCAAATCGCTGACCAGCAAATTTATAAGCAATTTGGCGTATCCGAATCCGAGTACGCATTAATCTGTGGATTTCTAGGCCGTCAGCCGAACTATACCGAGATTGGCGTATTCAGCGTTATGTGGTCGGAGCACTGCGCATACAAGAACTCGAAACCGCTGCTTCGCCGCTTCCCGGTAACGGGAGAACGCGTCCTGATGGGACCGGGCGAAGGCGCAGGGATCGTCGATATCGGCGACAATCAAGCGGTTGTATTCAAAATCGAAAGTCACAATCACCCTTCCGCGGTTGAGCCGTATCAAGGCGCAGCGACAGGGGTGGGCGGGATTATCCGCGATATTTTCTCCATGGGCGCAAGACCTGTGGCGCTACTAAATTCACTCCGTTTCGGTAAATTAGAATCCGAGCGGGTCAAATATTTGTTCGAGCATGTCGTGTCCGGGATTGCGGGATACGGGAACTGTATCGGGATTCCAACGGTTGCAGGCGAAGTCATGTTCGATGAGAGCTATGAAGGCAATCCACTTGTCAATGCGATGTGCGTAGGGTTAATCGACCACGATAAAATCCAACGCGGCGTAGCCAAAGGGATCGGCAACCCGGTGTTCTACGTTGGTCCTCCAACTGGACGCGACGGAATTCACGGTGCGACGTTCGCATCGGAAGAATTGACGGCTGAGACGGAAGCGAAGCGTTCGGCGGTGCAAGTCGGCGATCCATTTATGGAGAAGCTGGTTATGGAATCCACGCTTGAGCTGATCAATGCAGGAATCGTCGTCGGGATTCAAGATATGGGCGCAGCGGGCCTTACATGCTCGAGTGCTGAGATGGCAAGTAAAGCAGGTAATGGCTTAGAGCTATACCTGGATGAAGTACCGCAGCGCGAGCCGAACATGACGGCGTATGAGATGATGCTCTCCGAGTCGCAAGAGCGGATGCTGTTCGTCGTTGAACCGAAGGACGAAGCGCAAGCGATGGAGATTTTCGAGCGTTGGGGCGTGATTTGTGCCAAAGTCGGTAAAGTAACAGACGACGGACGTCTGCGTCTGATCCACAAAGGCGAAGTGGTCGGCGATATGCCGGTTCAAGCGCTTGTTGACGAGTGTCCGGTATACAACAAACCATCGGCAGTACCAGCGTATTACACAGCGAACGAGAACGTAGACACGACGCGTTACGAAGAAGTGACGGATTTGAACCGCGCATTGGAGCAAGTACTTGCTTCTCCAACGGTAGCGAGCAAAGAATGGGTCTACAATCAATATGATCACATGGTACGCACGAACACAGCAGTTCGTCCGGGTTCGGATGCGGCTGTCGTGCTCGTAGAAGGCACGCGCAAAGGTCTGGCAATGACAACGGACTGTAACGGCCGTTATGTCTACCTGGATCCAGAAGTCGGCGGACGGATCGCAGTCAGTGAAGCAGCGCGCAACATCGTATGTTCCGGTGCTGAGCCGCTTGCGATTACAGATAACCTGAACTTCGGCAGTCCGGAGAAGCCGGATATTTTCTGGCAAATGGAACGTGCTGTAGACGGCATGGCAGAAGCTTGCCGCGAGCTCAATACGCCGGTAATTGGCGGTAACGTGAGCTTGTACAACGAGAATAAGAAGGGCGCGATCTATCCGACACCTGTTGTAGGGATGGTTGGCCTTGTACATGATACGGATCATATTACGACTCAAGCATTCAAGAACGAAGGCGACGTGATCTTCCTACTCGGGGAGACGCATGCAGAGCTTGGCGGAAGCGAATTCCAATATGTCGTGCATGGCGTAACGGAAGGCAGACCTCCGCAGTTGGATCTGGCCACGGAACGTACATTGCTGAACTCGGTGCTTGGCGCGATTCAGCAAGGACTAGTGGCATCGGCGCATGATTTGTCCGAAGGCGGTATTGCTGCAGCGGTAGCAGAGAGCTGCATTAGCGGCAGCATCGGCGCATCGGTCAATATTGCAACGGAGTTGCGTCCGGATTTCGCGCTATTCAGCGAGAGCCAATCTCGTATTCTATTGACGGCATCGGCAGCACAGGCAGAAGCATTAGCGGCTTATGTACGTGAACAAGGTGTTCCTGTTCAGCGAATCGGAACCGTGCAAGGCAGCGATCTGACGATCACAGTGAACGGCAAACCAGGGGTCGCGGCACCTGTATCTCAATTTGCGAAGGTCTGGAAGGATGCGATTCCATGTCTCATGAAATAAAATCCTCCGAAGCGATCGCTCCGAAGTTATGGGTCGGCGATTACTACAACGAGGGAATGGGCCGGGACGATATTTTCGATAAGTTAAAAGAAGAATGCGGCGTGTTCGGGGTGTTCGGTCACCCCGACGCAGCGTCCTTGTCTTATTATGGTCTCCATGCCCTGCAGCATCGCGGCGAAGAGAGCGCGGGAATCTGCACGACGGACGGCGGTGATTTCAACTATCATCGCGGGATGGGTCTTGTAAAAGAAGTGTTCGATAAGGATCGCTTGGCGTCCTTAGTCGGCTCTCGATCGATCGGCCATGTTCGTTATTCGACGTCAGGGGAGAGTAAGCTGGCGAATGCGCAGCCGCTCGTATTCAAATATCGGGATGGCGATCTGGCGATCGCAACGAACGGCAATATCGTGAATGCCAATCAAATCCGTCGCGAGCTCGAGTCTTCGGGTTCGATCTTCCAGACGTCGAGCGATACGGAAGTACTGGCGCATTTGATCGCACGATCGCCGAAGGATTTCGTAACGGCGACGAAAGAAGCCCTGCAGAAGCTGGTCGGCGGTTTTGCCTTCCTCATCATGACGAATGATAAGCTGATCGTTGCTTCCGATCCGAACGGACTTCGTCCGATAACGATGGGACGACTCGGGGATGCGTATTTGTTCGCTTCGGAGACTTGTGCATTCGAGGTTGTAGGAGCGGAGCAAATTCGTGACATTCAACCGGGAGAAATGCTCATTCTGGATGCGACAGGGATGAAGGAAGATCGTTACACCGAGATGCAGCGCCGTTCGTTATGCGCGATGGAGTATATTTATTTCTCCCGTCCGGATACGGATTTGAACGGTTCGAATCTTCACGCGGCTCGCAAACGGATGGGCAAGAAGATGGCGCAGGAATCCTTCGTGGATGCAGATATCGTCACAGGGGTACCGGATTCCAGTATCTCCGCGGCGATCGGATATGCAGAAGAGACAGGTATACCTTATGAGTTAGGGCTCATTAAAAACAAATATACTGGCCGTACCTTCATTCAACCGAGCCAAGAGCTGCGGGAGCAAGGCGTGAAGATGAAGCTGAGCGCCGTCCGCAAAGTCGTGGAAGGTAAACGCGTCGTCATGATCGACGATTCGATCGTACGCGGCACCACGTCTCGCCGGATCGTGAACTTGCTGCGGGAAGCGGGTGCGACGGAAGTGCATGTGCGGATTACGTCGCCGCCGTTTAAGAATCCATGCTTCTACGGGATTGATACCCCAAGCCGCAAGGAATTGATCGCCTCTTATCAATCGATCGATGAGATTCGCCGGGAGATTAATGCAGATTCGCTTGCTTTTCTAACGAAAGATGGCTTGATTGAAGCGATTGACAGCTACTCGACGAACGAGATGAACGGCGGTTTGTGCCTGGCATGTTTTGATAATGATTACCCAACAGAAGTGGAGTTCCACGGAACAGAGAAATTCGGTTGCGGATGCGACTGATCGAATAGATATGACGAGTACAAAGAGAAAGACCACCAGAATGTAAAGGAGTGTACATGATGTCCTCAGAAGCCTACAAAGAAGCCGGCGTCGATATCGCGGCAGGAAATGAAGCGGTCGAGCGCATGAAGAAGCATGTCAAAAGAACGTTCCGTCCTGAGGTGATGACTGACCTGGGAGGATTCGGCGGCTTGTTCGGATTGAACAAAGACAAATACGAAGAGCCAGTTCTCGTATCCGGTACCGACGGTGTAGGGACGAAGCTCAAAATTGCATTCGCGATGGATAAGCACGACACGATCGGGATCGATGCAGTGGCGATGTGCGTCAACGATATTATCGTGCAAGGGGCAGAGCCATTGTTCTTCCTCGATTACTTGGCTTGCGACCGTGTCATTCCGGAGAAAATCGAAGCGATTGTCAAAGGAATTGCAGATGGCTGCGCAGAATCAGGTTGTGCGCTGATCGGCGGCGAGACAGCAGAGATGCCGGGTATGTACGCAGAAGGCGAGTATGACATTGCGGGCTTTACGGTCGGGATTGTCGATAAAAAGAAAATCATTGACGGCTCCACGATTGCACCTGGGGATGTTGTTCTTGGTCTAGCATCGAGCGGCGTACACAGCAACGGATTTTCGCTGGTTCGTAAGCTATTGCTAGAGAAGCATGGTTATCAATTGACAGATGCGCTGCCTGAGCTTGGTGGTGCAACACTCGGCTTGACACTGCTCGAGCCGACGAAGCTCTATGTGAAGCCGATCCTGAAACTGATCGAAGAGGTACAAGTGAAAGGCATGGCTCACATTACGGGCGGAGGCTTCATCGAGAATATTCCTCGTATGCTTCCTTCGAACGTGAACGTGAATATTGAATACGGCACATGGCCAATTCTGCCGATCTTCCAGTTGATGCAGCAGAAAGGCGAGATCACGAACCGTGACATGTTCACGACGTTCAACATGGGGATCGGGATGGTTATCGTCGTACCTGCGGATCAGGCTGATCAAGCTGTTGCTGTACTCAATGTGCAGGGCGAGCAAGTCTATCGCTTAGGCTCCGTTACTGAAGGAGAGCGTGTGGTCACCTTCACAGGAGCGGACGTGTAATGGAACGATTGCGTGTGGCGGTGTTTGCTTCCGGGAACGGAAGCAATTTTCAAGCGCTGGTCGACGCGATCGAGGCAGGACAGCTCCATGCGACCATGGAGCTGCTCGTCTGTGATCGGCCGTCCGCCCTCGTGGCGGAGCGAGCAGCGCAGGCAGGCGTGGACACCTTCTTGTTCTCGCCGAAGCAGTACCCGAATCGCGAAGCGTACGAAGCGGAAATCTTGAAGCAGCTAGAGGCAAAGAAGATTGATCTCGTCGTGTTGGCGGGGTATATGCGGATTATTACCGATACGCTCGTCAAGCCGTTCTATGGCCGTCTGATCAATATCCATCCGTCGCTGCTGCCTGCTTTTCCCGGCATGAACGCGATTCAGCAAGCACTGGACTACGGAACGAAGGTGACGGGGGTCACGGTTCATTTCGTTGATGGCGGCATGGATACAGGTCCGATCATTGCACAGCGTGTTGCCCTGATTGAAGAGGGAGCAGGGATAGAAGAGGTTACACAGTCGGTTCAACGTATCGAACGCGAGCTGTACCCGCAAGTGGTGCAGTGGTTCTGCGAAGAACGTATACAACTAATCGATCGAATTGTTCATATAAATTCATAGCATGGGAGGAATCAGACGTGGCTATTCGTAGAGCGCTGATCAGCGTATCGGATAAGACGGGGATTGTAGATTTTGCACGTGAGCTTGCGGCAGCAGGGGTAGAGATTATTTCGACGGGTGGCACGAAGAGCCTGCTCGAGAAGGAGAATGTTCCTGTGATCGGGATCTCCGAAGTAACAGGATTTCCGGAGATTATGGACGGCCGTGTCAAAACATTGCATCCAGCGGTTCACAGCGGCTTGCTCGCAGTGCGTGACAATGAAGAGCATACGGCACAGATGAAAGAGCTTGGGCTTGATTATATCGATATCGTGGTCGTGAATTTGTATCCGTTCAAAGAAACGATTGCTAAACCGGGCGTCTCATACGAGGATGCGATCGAGAATATCGATATCGGCGGACCGACGATGCTGCGTTCCGCTGCGAAGAATCACGCGTTCGTCACCGTGGTTGTGGATGCAGCGGATTATGCGCAGGTGATCGAGGAAGTACGTGCTGGCGGCGATACGACACTTGAGACTCGTAAACGCTTAGCGGCCAAAGTATTCCGTCACACGGCAGCATACGATGCGCTTATCTCGGACTACCTCTCCAAGCAAGTCGGCGAGCCATTGCCTGAGACGTTCACTGTGACGTATGAGAAGGTGCAGGACCTACGATATGGAGAGAATCCGCATCAGAGCGCGGCGTTCTATCGCAAACCGCTCGCAGGCCTAGGCAACATTACGACAGCAGAGCAGTTGCACGGCAAAGAACTATCCTACAACAACATCAACGACGCGAACGCAGCGCTCTCGATCGTACGTGAATTCGATGAGCCTACGGTTGTCGCGGTGAAGCATATGAACCCATGCGGCGTGGGCATCGGCGAGACGATCCACGAAGCGTATCAGAAAGCCTACGCAGCTGACCCGACTTCAATCTTCGGCGGTATCGTGGCTGCAAACCGTGTGATCGGCGCAGAGACAGCATCGTTGCTTGGCGAGATCTTCCTTGAGATCGTGATGGCGCCAGACTTCACACCAGAAGCATTCGATATTCTGGCGAAAAAGAAAAACATTCGTCTATTGAAATTAGGCGAGTTCTCGGCTTCTGCTGATCGCAAGACCGAATTCGCGGTGACATCGGTTGATGGCGGCATGCTCGTCCAAGAGACAGATATCCGTCAATTGGATGAGTCAGACCTGAAAGTAGTAACTGATCGTCAGCCAACGGCAGAAGAGCTGAAGCAGCTCTTGTTCGGTTGGAAAGTTGTGAAGCACGTAAAATCCAACGCAATCGTATTAGCCAAAGACGATATGACAATCGGTGTAGGTGCAGGCCAAATGAACCGCGTCGGTGCAGCGCGTATCGCAATTGAACAAGCTGGAGAGAAAGCGCAAGGCTCCGTACTCGCTTCCGACGCATTCTTCCCGATGGGCGACACCGTTGAACTGGCTGTCAAAGCTGGCGTAACGGCAATCATCCAACCAGGCGGGTCGATCAAGGACGAGGAGTCCATTCGCGTGGCGAACGAGCACGGCATTGCGATGATCTGCACAGGTGTGCGTCATTTCAAGCATTAA

Protein sequences of DBSCAN-SWA_4

>NZ_CP045293|6309164:6324370|6314764_6315646_+|WP_152396547.1|DBSCAN-SWA
MSVRAISTAVDLVKAPLLYKGKVRELYDLGEHYLIVVTDRISAFDYVLEPAVPEKGNVLNRLTAFWFEQTAAIEPNHVVHTDVEKLGDLVTEPELLKDRIMVTKKAERIDIECVVRGYITGGGWRQYQQSGSVNGIALPAGMKKNERFAAPIFTPAAKNDVGHDEDISFDRMKELVGEELAHELQMKSLQLYSFAHAYCEKRGIILADCKFEFGLIDGQVILIDELFTPDSARFWVKENYALNIEIDSMDKEPVRTYLANSDWDKNSVPDPLPAEVVAETTHRYQDIYRRLTE
>NZ_CP045293|6309164:6324370|6313444_6314740_+|WP_152396546.1|DBSCAN-SWA
MLERYSRPEMRAIWTEENKFNSWLEVEICACEAWAELGVIPKEDVATLRKNASFNIDRIYEIEQETRHDVIAFTRAVSESLGEERKWVHYGLTSTDVVDTALGYVLRQANEIIEKDILQFIDILKTKALTYKHTPMMGRTHGVHAEPTTFGLKMALWYEEMKRNLERFRHAANGVQYGKISGAVGTYANIDPFVEKFVCEKLGTTAAPISTQTLQRDRHAEYMATLALIATSLDKFATEIRALQKSEVREVEEAFAKGQKGSSAMPHKRNPIGCENISGLARVIRGFMVSAYENVPLWHERDISHSSVERVILPDATMLLNYMLNRFGNIVKNLTVMPENMKRNMERTFGVPFSGRVMTKLIDKGMSREQAYDTVQPRAMQAWEEQRSFREIIEATPEIATVLSAEEIADAFNPAWHLKHVDTIFAQLGLE
>NZ_CP045293|6309164:6324370|6322822_6324370_+|WP_152396553.1|DBSCAN-SWA
MAIRRALISVSDKTGIVDFARELAAAGVEIISTGGTKSLLEKENVPVIGISEVTGFPEIMDGRVKTLHPAVHSGLLAVRDNEEHTAQMKELGLDYIDIVVVNLYPFKETIAKPGVSYEDAIENIDIGGPTMLRSAAKNHAFVTVVVDAADYAQVIEEVRAGGDTTLETRKRLAAKVFRHTAAYDALISDYLSKQVGEPLPETFTVTYEKVQDLRYGENPHQSAAFYRKPLAGLGNITTAEQLHGKELSYNNINDANAALSIVREFDEPTVVAVKHMNPCGVGIGETIHEAYQKAYAADPTSIFGGIVAANRVIGAETASLLGEIFLEIVMAPDFTPEAFDILAKKKNIRLLKLGEFSASADRKTEFAVTSVDGGMLVQETDIRQLDESDLKVVTDRQPTAEELKQLLFGWKVVKHVKSNAIVLAKDDMTIGVGAGQMNRVGAARIAIEQAGEKAQGSVLASDAFFPMGDTVELAVKAGVTAIIQPGGSIKDEESIRVANEHGIAMICTGVRHFKH
>NZ_CP045293|6309164:6324370|6316696_6317386_+|WP_152396549.1|DBSCAN-SWA
MNFAVIVFPGSNCDIDCYKAVEQTVGQPVDYVWHTATDLSKYDCILIPGGFSYGDYLRSGAIARFAPVMTEVAKAAAAGKYVMGICNGFQVLTEAGLLPGALRRNVSLKFRCHSTILRVENNQTAFTNQYEVGELIDIPIAHGEGNYYCDEATLEQLKKNNQIIFRYSDNPNGSLEDIAGICNEQGNVLGLMPHPERAVNQLLGSEDGKKMFTSILNAWREQHDAASIG
>NZ_CP045293|6309164:6324370|6321147_6322194_+|WP_152397472.1|DBSCAN-SWA
MSSEAYKEAGVDIAAGNEAVERMKKHVKRTFRPEVMTDLGGFGGLFGLNKDKYEEPVLVSGTDGVGTKLKIAFAMDKHDTIGIDAVAMCVNDIIVQGAEPLFFLDYLACDRVIPEKIEAIVKGIADGCAESGCALIGGETAEMPGMYAEGEYDIAGFTVGIVDKKKIIDGSTIAPGDVVLGLASSGVHSNGFSLVRKLLLEKHGYQLTDALPELGGATLGLTLLEPTKLYVKPILKLIEEVQVKGMAHITGGGFIENIPRMLPSNVNVNIEYGTWPILPIFQLMQQKGEITNRDMFTTFNMGIGMVIVVPADQADQAVAVLNVQGEQVYRLGSVTEGERVVTFTGADV
>NZ_CP045293|6309164:6324370|6322193_6322805_+|WP_152396552.1|DBSCAN-SWA
MERLRVAVFASGNGSNFQALVDAIEAGQLHATMELLVCDRPSALVAERAAQAGVDTFLFSPKQYPNREAYEAEILKQLEAKKIDLVVLAGYMRIITDTLVKPFYGRLINIHPSLLPAFPGMNAIQQALDYGTKVTGVTVHFVDGGMDTGPIIAQRVALIEEGAGIEEVTQSVQRIERELYPQVVQWFCEERIQLIDRIVHINS
>NZ_CP045293|6309164:6324370|6311780_6312266_+|WP_152396544.1|DBSCAN-SWA
MSVQVGVIMGSQSDWETMKHACDVLDELGIAYEKKVVSAHRTPDLMFQYAESAVERGLKVIIAGAGGAAHLPGMVAAKTILPVIGVPVKSSTLNGLDSLLSIVQMPGGVPVATVAIGNAGATNAGLLAAQIIGAFDPAVQRRVQSRRDAIRDHVLEGSDSL
>NZ_CP045293|6309164:6324370|6309164_6311312_+|WP_152396543.1|DBSCAN-SWA
MKTLVLAEKPSVAREIARVMGSNQKHKSYFEGPKYIVTWALGHLVGLAEPEDYDVKYRTWELEHLPIMPEKMKLKVLRETSHQFKAVQQLAGRQDVADLIIATDAAREGELLARWIMAMVKWKKPFHRLWISSQTDKAIREGFANLKPGSQYNRLYESARCRAEADWLIGLNVTRALTCKFNAQLSAGRVQTPTLGMIMDRENEIRNFRSAEYQTLQGEFEGFQAQWRPRGGQGDGRMFDPNQAEALRKKVDGKKGKVTLVKKSEKSEPHPLAYDLTELQRDANKRYGFSAKQTSNVLQRLYEQHKLVTYPRTDSRYLSSDMTDTLPERIRSVAVGPYAAIAKPLLRGKLPITRRVVDDSKVSDHHAIIPTDQTVLLNALSNEERKLYDLIVRRFLALFYPAAKYELTALTIEVEGETFMTRGKTVIQNGWREVYGQEDSWDDDEDESGADRDDDRSGIQLLPSLREGEAVQMKRANLRKDRTQPPKRYTEASLLGQMEKYGLGTPATRADIIEKLVSSDTIERQGASLHPTGKGVQLIELVASELRTPELTAKWEQELEKIARGQGGTEPFMKGIRDMAQSLVSGVKTSDAAYKPHNLLNSRCPECGEKMMEKKGKRGKMLVCSSGDCSYRRSGEKQLSNRRCPQCHKKMELKDGKAGKYVQCLGCNVIEVLDGERGGRVNKREQQKLVKQFEKTESMGSSLGDALRAALERKE
>NZ_CP045293|6309164:6324370|6319591_6321088_+|WP_152396551.1|DBSCAN-SWA
MSHEIKSSEAIAPKLWVGDYYNEGMGRDDIFDKLKEECGVFGVFGHPDAASLSYYGLHALQHRGEESAGICTTDGGDFNYHRGMGLVKEVFDKDRLASLVGSRSIGHVRYSTSGESKLANAQPLVFKYRDGDLAIATNGNIVNANQIRRELESSGSIFQTSSDTEVLAHLIARSPKDFVTATKEALQKLVGGFAFLIMTNDKLIVASDPNGLRPITMGRLGDAYLFASETCAFEVVGAEQIRDIQPGEMLILDATGMKEDRYTEMQRRSLCAMEYIYFSRPDTDLNGSNLHAARKRMGKKMAQESFVDADIVTGVPDSSISAAIGYAEETGIPYELGLIKNKYTGRTFIQPSQELREQGVKMKLSAVRKVVEGKRVVMIDDSIVRGTTSRRIVNLLREAGATEVHVRITSPPFKNPCFYGIDTPSRKELIASYQSIDEIRREINADSLAFLTKDGLIEAIDSYSTNEMNGGLCLACFDNDYPTEVEFHGTEKFGCGCD
>NZ_CP045293|6309164:6324370|6316446_6316692_+|WP_152396548.1|DBSCAN-SWA
MFKATVYVTVKENVLDPQGVAVQGALHSMGFSEVSKVRIGKYMAFEVDTTDRAEAEERVRQMCEKLLANTVVEDYRFELEG
>NZ_CP045293|6309164:6324370|6312262_6313444_+|WP_152396545.1|DBSCAN-SWA
MIEKNMITSVERIIAPGSTIGVLGGGQLGRMMALSGSNLGYRFVTLDPMPDGPCGQVAEQIIAAYDDQDAARKLADEADVITYEFENVDAGVAAMLMSESYVPQGSELLYTTQHRLREKRAIEAAGVRVAPYAEITSEEDLRAAVDRFGLPCVLKTATGGYDGKGQWVIRSADEIPEAYATLAAAKTELVLEQFIRFTKELSVIAARSPRGEVKVFPVAENIHVDNILHQSIVPARVSFDIQDRAEALAIRIAESMNVVGLIAVELFLTEDGELFVNELAPRPHNSGHYTMEACRTSQFEQHVRAICNLPLGDTMLLTPVVMVNVLGEHVEPLLAHMVQEDEAAEAFNVAPKVHLYGKKEAKVKRKMGHVNVLADHLDDALAWIEKTQIWRNH
>NZ_CP045293|6309164:6324370|6317363_6319607_+|WP_152396550.1|DBSCAN-SWA
MTQQVSAKEPTAQQIADQQIYKQFGVSESEYALICGFLGRQPNYTEIGVFSVMWSEHCAYKNSKPLLRRFPVTGERVLMGPGEGAGIVDIGDNQAVVFKIESHNHPSAVEPYQGAATGVGGIIRDIFSMGARPVALLNSLRFGKLESERVKYLFEHVVSGIAGYGNCIGIPTVAGEVMFDESYEGNPLVNAMCVGLIDHDKIQRGVAKGIGNPVFYVGPPTGRDGIHGATFASEELTAETEAKRSAVQVGDPFMEKLVMESTLELINAGIVVGIQDMGAAGLTCSSAEMASKAGNGLELYLDEVPQREPNMTAYEMMLSESQERMLFVVEPKDEAQAMEIFERWGVICAKVGKVTDDGRLRLIHKGEVVGDMPVQALVDECPVYNKPSAVPAYYTANENVDTTRYEEVTDLNRALEQVLASPTVASKEWVYNQYDHMVRTNTAVRPGSDAAVVLVEGTRKGLAMTTDCNGRYVYLDPEVGGRIAVSEAARNIVCSGAEPLAITDNLNFGSPEKPDIFWQMERAVDGMAEACRELNTPVIGGNVSLYNENKKGAIYPTPVVGMVGLVHDTDHITTQAFKNEGDVIFLLGETHAELGGSEFQYVVHGVTEGRPPQLDLATERTLLNSVLGAIQQGLVASAHDLSEGGIAAAVAESCISGSIGASVNIATELRPDFALFSESQSRILLTASAAQAEALAAYVREQGVPVQRIGTVQGSDLTITVNGKPGVAAPVSQFAKVWKDAIPCLMK

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_152396543.1|6309164_6311312_+	DNA topoisomerase III	A0A0G2Y4W4	Acanthamoeba_polyphaga_mimivirus	1.3e-26	25.7
WP_152396544.1|6311780_6312266_+	5-(carboxyamino)imidazole ribonucleotide mutase	A0A2P0VNU7	Tetraselmis_virus	1.1e-21	41.5
WP_152396545.1|6312262_6313444_+	5-(carboxyamino)imidazole ribonucleotide synthase	NA	NA	NA	NA
WP_152396546.1|6313444_6314740_+	adenylosuccinate lyase	A0A2H4UUU6	Bodo_saltans_virus	5.9e-19	25.8
WP_152396547.1|6314764_6315646_+	phosphoribosylaminoimidazolesuccinocarboxamide synthase	A0A0M4JBD3	Mollivirus	2.3e-35	32.3
WP_152396548.1|6316446_6316692_+	phosphoribosylformylglycinamidine synthase subunit PurS	A0A0E3FJ99	Synechococcus_phage	3.1e-06	34.6
WP_152396549.1|6316696_6317386_+	phosphoribosylformylglycinamidine synthase subunit PurQ	NA	NA	NA	NA
WP_152396550.1|6317363_6319607_+	phosphoribosylformylglycinamidine synthase subunit PurL	A6N228	Microbacterium_phage	2.1e-165	43.7
WP_152396551.1|6319591_6321088_+	amidophosphoribosyltransferase	A0A0M3SGR2	Mollivirus	1.2e-50	32.4
WP_152397472.1|6321147_6322194_+	phosphoribosylformylglycinamidine cyclo-ligase	Q58MH8	Prochlorococcus_phage	8.3e-72	46.2
WP_152396552.1|6322193_6322805_+	phosphoribosylglycinamide formyltransferase	M4QRX9	Synechococcus_phage	1.4e-23	37.5
WP_152396553.1|6322822_6324370_+	bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase	Q58MG4	Prochlorococcus_phage	1.1e-75	52.0

2. NZ_CP045294

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	33891 : 44280	12	Clostridium_phage(37.5%)	tail,plate,portal	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP045294|33891:44280|DBSCAN-SWA
TATGGGATTACCGAATGTGAACATTATTTTTAAGCAAAAAGCCGCGTCCGCGGTACAGCAAGGGGCTGTCGGCGTCGTCGCGATCGTCTTGAAGGACGCGTCCGTGTCTGCGTTAACAAGCTATGAATTGCATGGCGCCGATGAGTCGCCGCAAGCTCTAAAGGCTCAGAACGCTGCCTATGTGCAGCAAGCGTTTATGGGGATGCCGAAGCTCGTGAAGCTGGTCGTCATTCCGGAGACGGAGACGGATTACAGCAAGGCGATGCAGTATCTCGAGACAATTGCGTTCAACGTCGTGGCGTTCCCTGGCGCAGCGACAGCCGACGTAACGGCGCTCTCCACTTGGGCCAAAAACGTCTTTACGAACAAAGACCGCAAGATTATCGCGGTGCTGCCGAACTCGGCGGCGGATCATCCATCCGTCGTCAACCTGGCGACCGACAATATCGAGGTTGGCGCTCAAAAATATACGGCTACGCAATATACGGCGCGGATTGCAGGTCTGATCGCGGGTCTGCCACTCACCGTGGCGCCAACGTTCCAAGTGCTGCCGGAGGTGACGAATGTGCCTTCCATGACGAAGTCGGAAGCTGACACCGCGGTAAATGCCGGGAAATTCGTGCTATACCACGACGGCGAGAAGGTTAAAATCGCGCGCGGCGTCACTTCGCTCGTGACGACGACGGAAGCGATGGGTGAGGATTGGAAGAAGATCAAAGTCGTACGCATCCTGAACAAAACCTATCAAGATTTGAAGGAAACGGTGGAAGATTTCTACGTAGGCAAGGTGCAGAACAGTTACATGAACAAGCTGCTGCTCATTTCTGCGATGAATGCGTATTACGAATCGCTTGAACAGGACGGGATCCTTGATCCAGGCAAAAATGCGGCTGAGATTGATCTGGCAGCACAGCGCACTTATTTGAAATCCATTCTTGGAACTGAGGTTGTCGCAGGCATGACGGATCAGCAAGTCAAAGAAGCGAACACGCGGGATAAAGTATTCATTATGGCTAGACAACGCCCGCTGGATGCAATCGAAGACGTCACAATGACGGTCTATCTATAAGGAGGAATGAACAATGGCAACTTTTAACGGTGAAAAAGTCATTTCGGGAACGTTCGGCGAGGCATGGCTCGACGGGCAGTATATTGCGGAGATTATGGCGCTGGAAGCCAAAATCGAAATCGAGAAGGAAGATGTGCCGATGGCGGGTCGTTTTGCGACGGACAGCAAGTTCATGGGCTTCAAGGGCAGCGGCACCTTGCGGATGCACAAAGTCAATTCGCGCTTGATCAAAGCGCTCAGTGATAACTTGAAGAATGGGGTGAACCCGCGGTTCCAGATCATGTCGAGCTTGAACGATCCGTCTTCCGGCGGTGCGGAGCGCATTACAATCAAGGATGCCAGCTTCAATGACTTGTCCCTGATCAACTGGGAGTTGAAGAAGAAAGGCGAGATTGAAGCGCCGTTCACGTTCACGGATTGGAATGTCGAGGATTCGATTAAACCTTAATTTTAGCGTGCAAAAGGAGGAAGTTAAGCTATGAGTCAATTATCTCTCGATTTGTTGTTAAAAATGGACAAGTCCAAAATTCAACGTCCTACAGCCAAAATCGAAATGAGTCGCTTAAGCGAGCTGGTCGGTGAGCCGGTGATCTTCACCTGCCAAGCGCTCACGATGGATGAGTTCGAGGAGGTGCAGGAGGTTTCGGTATCGTTTGGCAAGAAAGGCGAACTGGAAGAGTTCAGCACGAATAAAGTGCAGATTTTTACACTGCTCAAGGGGATCGTCGATCCGAAGTTGTCCGATTCGAAATTGCTCGAAGCGTACGGCGTGACGACACCGAAGCAGTTGATCGAAGAGTCGAAGCTGCTCTTGCCGGGCGAAGTGACGCAATTGTACAACGTGATCTCGAGCCTGTCGGGATTCGGGGATGAAGCGGTCAAAGAATTAAAAAACGGATAAAATCGGACGGCTACGTTGAAATGCTCTACTACTATTGGAGCCGCAGAGGGATGCGCCCGAGCGAGTTCTATAATATGCCGGCAGGGGAGCAGTGGCTGATCCGAGTGTTCTACGAGATGGAAATGGAGGAGCGGGAACGAATAGCGAAGACGGGGAATGTCTTCGCGACCCTTCCCGTTCTCTAGGGAGGTGAGAATGGAATGTGTGGATCGAATGGAGAGAAGAAATCTTGCAGCAAATGCAATAAAGCGAGCAGCGACGGCTCAGCGAATATATCGCTGAAGCATGCGCTGTTCCAAGTGCAGATGGTCCAGCGGCAGGTGGATCTGCTGAAGAAGTCGATGCGCAATATGCAGATGAACATTCAGGTAAAGACGAATGTCGTGCGCAAGCAAATGCTGGATATGAAGGCGCAGATCGAGGGTACAGCAAAGTTCAACATTGAACTGGTTGCCGAGCCGAAGATCAAATTGGACTGGAAAGATATGCTGATGAAAGCTGGTATTTTCATTGCGACACTCGTGGCGCTCAAGATCGCTATCAAGAAGTTGGGCGGCAGCGCAGAATTTAAGATCAAATACTCGATCGAAAAAATGAAGCCGAAGCGGACGAAGGCGACGCTGATGAATCCACCCCCAGTGGGTCCGAAGTATCCTAGCGGAGACGAAGGCGGACTTCCACCAAGAAGGAATAGGAGTGGAGGTAAACGCGGTGGGAAAGGTGGCAAAGGCGGCGGTCTACTAGGTGGTTTAGGTGGATTGCTCGGCGGATTAGGCAAAGGGCTTGGCGGCCTCGGCAAAATGCTGAATCCGTTCAAGCTGATCGGCAAGATTGTTCCGATGTTCAGGCTGCTCGGGCCCGTGATCTCGAAGCTGTCGCCGCTGGTTGCGAAGCTGGGGGATGCATTTCTGAAAGGGATGGGGAAAAGCTCAGGCATCATTAAAAAGGTGAGTACTCTGATTGGTTCTTTTCAGAGTGTGCTCATCAACTTGGTTACCATGGCGGGACAACGGTTTGCGCAATTCATCGCGTGGCTGCAGCCGGCACTTCCGACGATCGTCGGATTTATCACGGGTGTAGTTCAGAAGGCTGTACAGTTCTTTGCGCCATTGCTGCCACCGATCATGCAGGTGTTCCAGACGGTATTCGGCTGGATTGTCGAGAACATGCCTGTGTTTCAAGCAGCGATCGGAAGTGTATTTAGCGCACTCGGCCCGATTATTCAGACGGTCGTGAATGTGTTCCAGATGCTCTGGGGCATTTGGATGGAGGCCTGGCCGACGATTCAATCGATTCTAGAATCGGTATGGGCTGTCGTGCAGCCGATCTTTGACGTCTTCATTACGATCATTCAGATTTTAATGAACGTGATTCAAGCGGTCTGGGATGCGCTGAAGCCGGTGCTCGAGATGATTTGGGAGGCGCTAAAACCAATTATTGATGGGATTGGCAGCATGATTAGTGCGTTTGGCGATGGCTTGGACTGGGTGCTCGATAAGGTATTTGGAGGCGGCGGAGGCAGCGGTCAAGACAGTGCAGTCGGAGGTGCCTCAGATCCAGCGAAGAAGCATGCGGCTGGTCTGCTTACGGTTCCGAGGGACAACTACCCGGCGCTGCTGCATCGTAATGAAGCCGTGCTCACAGCACGCGAAGCCAATCAATATCGCAATGGCGGAGCGGGGCGCGGCATTACGATCAATCTGAATAATCCAGTGGCACGTGAGGAAGCCGACTTCAAGAAATGGGCAGTCATCCTGCGCACAGAGCTGGAAAGTGCGGGCTTGAACATGGCTTAGGAGGAGGTGAGAAGGAATGATCGAATTTTGGTTGACGTTCAACAACAATGAAGAATCCATATGGCTGCACATTCCGCCGCCGTCGTTCGAGATTCAGACGGGGTTATGCAATTCGACAGTCACCTTGCACGAATTGGGCGAGTTAATGCTAACGGGCAAGCGCAGGCTGAAGACGGTGTCGTTGAGCAGTTATTTTCCAGTGGTGGACGATGGGCTTGGTCAGTATAAGTCGCCGAAGCCGCCAAAGGAGCTTGTGAAGATGATTGAGAACTGGCGGGACAGCCAAAAGCCGATGCGGCTGCTGATTTTCGGCAAGGGGCTTGTCGTCAATGAAGCGATGGTGATTGAGAATTTCTCGTATTCGCAGAAGAATGGACCGGAGGATGTCTATTTTACGCTGGACTTGAAAGAGTATCGGTTCGTGAAGGTGAAGACAACACCCCTGAATGCGAAGGAAGCGGAGCAATTGCGGCCGCGTCCGTCAGATCGTGGGCTGGCCAAGACGTATACCGTTCAACCGGGAGATACGCTGAAGAAGATCGCGAAGAAAGTCTATGGCGATGAATCCAGGTCAATCACGATTAAGGAGACGAATCATATTACGAGCGAATACAGCCTGAAAGTAGGCATGCAGCTAAAGATCGGATAAAGGAGGGGGTGGCATGCGGATTGTCTATATATCCCGAACGAATCAGAAGTCGGATATCACCGAGTTATTCATTCGGGCGACATGGAGCGGCGACGTCAAGGAAGTGGCGCGCAAGCTGGAGGTATCGTTTGCGGTGAACGCGGGTGAACCTTACCTTCCTAAGCTATTCATGGACCTAGGAGAGATGCTGATGGTCATCGATGATGAGGGGAAGGAGCTGTGGCGGGGGTATATTTTCGCGAAAAGCAAGTCTTTGTCCGGCACGGAGGTGACATATACGGCGTATGACGGCTTGATCTATCTAACGAAGTCCAAGGTATCGAAGAACTTCAAGCAAGTGACGGCCGAGCAGATCACGAACTTGCTGTGCAAGGAGTTCGGTATCCCGGTTGGGCAGCTCGCGAAGACGAATATCCCGCAGAGCTTCGTACATATGGGTAAGACGGTGTATGAAGCGATCATGACAGGATACACGCTGGCGTCCAGCCGGACCAAGCGCAAATATATGCCGCGGATGCGAGAAGGCAAGCTGGATGTGGTACTGCTCGGCGAGACGGTCGTGAAGCGCATCCTGACGGCAGAGACGGATCTGCTCGAATCCACAGTGGACGAGAGCATCGATGCGATGGTTAACCGTGTGTTGATCGTCAATGAGGCGGGCAGCGTTGAACGGGTCGTAGACAATGGACCGTGGGTCGAGAAATATGGCCAGATGCAGGAAGTGTACCAGAAGGAAGAAGGTAAAGATGCGAACCAGGAAGCGAAATCTAGACTATATGGTATGGATCGTAGTGCTTCGGTTCAGGTTATCGGCGGGCGGGATGCTTATGATCTGGTCGCTGGAAATGCGGTGCGAATGATCGAGGATGTGACCGGGATGACCGGTCTTTTTTATATCGAAAATGATTCGCATTCGTTTGAAAATGGTGTGCACACCTTGAATTTACAGCTCAATTTCGAGAAGGTCATGGACGAATATATGCCGGATGAGCAAGGGGGAATTTGATGTCCGAGTTGTCATGGCTCGTTGAATTTATTCGGGATCAGGGACAGAAGTCGATGGGTCCTTCGGTGTTGCTGGGTCAGGTGCTCACGGTTCCGCCCTCGTTGGTGGTTCGTGTGCAGGGGATGGATCTCATGGTAGAGGATCTCTATATCTCTTCTTCGTTGCTTCTTCCGGATGCGTTACGGATCGGGGATCGGGTTACATTGATGCCGCTTGCCGGAGGACAGCAATTTATCGTATTAAGCAAGGTGGTGAAGATGGGTGAATGATCTATTTCCGATGGTGGATGTCCCGCCGGATATAGCTGTTGGTGTTGGTAGCGGAGCAAGTTTGCCGTTATTCCGGGAATATGCATGGGATTTCGATCGGGATGAATTTGTGATGAAGGATGGGCAGTTGGTGCTGCTCGAAGGTCAGGCAGCTGTGCAAGTGTGGGTATATAAGGCGCTGCGTACCGAGCGTTATCGGTATTTGGCGTATACCTGGGATTATGGCAATGAGATCGAGAGGCTCATCGGCAGCACGTTCTCGCCTGCTGCGCAGCGCAGTGAAGCAGAACGTTACGTTCGTGAGGCGTTAATGGTTCTCCCATACATTCGGGAAGTGAACCAAATCGAGATCGCATCGGAAGGCGATGAGCTGCGTATCGAAGCGACGGTCGAGACCGTCTATGGGGAGGTGAAGGTGCGTGTTTGAACAACAATCTTGGGATAGCATTCTCGCACGGATGCTGAACCGATTTGCCCCGCAAGGGGTGGCGAAGCAGGAAGGCAGCTTTGTCTATGACGCAATGTCGCCGGTCGCGGTGGAATTGTCGCAGGCATATAGCGATTTGGATCGCGTGCTGGAGCAGGGGTTCGCTGAGACGAGCAACGGGGTGTATCTGGACCGGCGTGCAGGTGAGCACGGTGTGACGCGCAAGCCGCCGGCGAAGGCGCACGGGATTGTGAAGGTGAGCGGAACGGCGGGTGCGAAGATTCCCGCGGGTGCGATGTTCGCAACGAAGAATGGCACGCTGTTCGTAGCGGCGGCCGAGGCAGTTATTACTACGGAAGGCTTCGTGAAAGTAAACGTGGCCGCGGAAGAAGCGGGTGTGAGCGGGAATGTGCCGGCACTGGGGATTACGGAGATTATCGGCAGTATCCCAGGCGTACAGCAGGCAGTGAACGAAGCGGCTTGTGCCGGAGGGTATGACGGGGAGACGGACGATGCCCTGTTGGATCGGCTGCTGACTAAGGTTCGTACACCGGCGACGAGCGGCAATGCGAACCAATATCGTCAATGGGCGATGGAAGTGACAGGTATCGCGGATGCCAAAGTGTTCCCGCTATGGAACGGCAACGGGACCGTCAAAGTCGTCCTGCTGGATGACAATCGGCGTGCGCCTGTACCAGAGCTGGTTACACAGGTTGCGAATCATATCGCATTGGTGAGGCCGATTGGGGCGAACGTGACCGTGTCGGCTGCCGTGGAGGTGCCGCTGAATATCGACGTGGACCTGGATGTCTTACCCGGCACATCACTTGAGGATGCCAAAGCGTTGATTACCAGTGAGATTATCGTGTATTTGAAGGGCCTTTCGTTCGTGGATCCGATCGTTCGGACTGCCCGTATTGCGAATGTCATCTTGGATACGAAATCGATCGTGGACTACCGCGACCTGAAGATTAACGGGAGCATGGAGAACATCATTATTCCGGAAGGCAGCGTCGCGGTGATCGGGACGGTGACTGTGCGATGACGGATGTAAGGGAAAGGGCAGTCATCGAAAGGGCTGTGGGGAATAATCCGCTACGTCGATATGTGCCAGAATTCGTATCGGGCTCGCGTATTCTTGGCGGTATGCTGGATTCGCAATATCAGGAGAATCAGGAGCTGACGGCATCGATTGACGAAGTGCTCGATCAATTTTATATCGAGACAGCAACGTGGGGTCTGGATCGGTGGGAGCGCATGTGCGGCATTGCGACCGACCCGTCCAAGCCGCTTGATCAACGCCGCAGTGTCATCAAGTCCAAACTGCGCGGGATCGGCACCGTCACAGTGGACCTCGTGAAGAACGTCGCCGAGGCTTTCGCGAACGGCCAGGTCGATGTACAGGAGGATGTCGCGAAGTACACAATCACTGTCACCTTCGTCGGCAAGCTCGGCATCCCGCCGAATATGGAAGACATCACCCATGCGCTGCGGGATATTATCCCGGCACATTTGGGGATTGAGTATGTGTATAAGTTCTATCCTTACTATGAATTAGCGAAGTCAGGGAAGAAGTATCAAGATCTAACGTCATTGACGTATTACAAATTAGTAGACAAGGGGGTTCAATAACATGGCAACAACACCCAAAATTAATCTCCCGCTGATCGATAGCTCAATGACCGCTGACATCCCACGCGATATGAACGCGCTAGCCAACGCCATTGACGCGGTGGTGGAGACTACTACGGGAGCGAAGACGAAGGTAGACCAAGCATTGGCTAGCGCGAAGGCTTACGTAGATGCAGACCTAAAAGAGGCTCCGGCGGTGCCGATCAACCTTAAGATGGGAATGCAGGTCATTGATGCGAAAGAGACGAGCCTTGTGAATATTACGGGGCTGAAGGGTCGGACGTTGGTGAATTTACTGGGGCGTGATGGGAATTGTGAGGATATGAGTAAGTGGTCATTAATCGGCACCACGGTTCTGGACACTGCGAATAAAACGTGCGGAATGAATGGATTTAAGAGTACGGTGACTAATGGAACATATGCCGATATCTGGCGTACGGTTGCATACGATAAGAATAAATACTATATTGCGCTGGCAGATATCAAGAACGGCAATGCTCTTAAAATGCGACTTCGCATGAATGATAATGTTGCCGTTAAAGAGATTATGTCCAGGGATGTTACGGAGACTTCTCAGTTTACTACTGCTTGGGTAAGAATCGAGCCTAACGCATTTACGGGTACTAATCCTGTGTATCTCAGTATTGTCACAGCAGGTGGTAATGGAAGTTATGGATATGTAGATGCAATCCGCCTATATGAAATTCCGAAAATGGAATATGAGGCATTGACCTCTATGGCAGATAGTCAAATCGCTGCCAAATACCCGTATGTCGATAGTTTGCAGAACGTAGCGAATCCATATGTGATTGGATATGGGGAGAATTTGTTGCCGCCGTTTATGGAATGGATACCTAGCGGTAATTTAACTCAGTATTCAGCACTAGCGCCCTACGAAGCTTCGACGGTAACGACTGGTGATTTTCAAGCATTAATTTCGCCGCAAATTCCAGCCGTAAAAGGTCAAACATATACGCTTAGTATTGAATCTCGAGCAGGTCGTATGGTAGTAGGTCAGTACGATAAGGCTGGTAATGTAATAGACTACCCTGTAGCAGAGGCGCAGAACGGACAAGGGGCCTTCTCAGCGACATTTACTGTTGCCGATAACGTATCTCACCTCGTCGTTCAATTATCCAACTATGGTGCGGGAACTTTCATTTTCAAAAAGCCGATACTCACGTTAGGCAGCACATCCAAGCCGTTTGTACTACGTCAAGATTCGATTCTCGCACTAACGACGGAACTAGCGTCCAACGTTGACGGGTCAATAGCTGACGAGCTTTTCACGAAGGACGGGCTATATTGGAAGCTGTCGAAGTACAAGAAGATTACGCTTGACGGGTCGCGAGATTGGAAGTTTAACGCTGTGAAATCTGGATTTAAACAGGTAAGACTGGAAGGCAATCAAAAAGCGTCAGGAAGTCCTGTTATACAGTACGCAACAAAGTATGACGGTAAAGCACTTAAATATGATGGCAATGTCACAGAAGGAGACTCCTTCAACGTTACCAGCACAAATGACGTCATATACATGGGCATATCTAACGCAGATAGTGGTTGGGGCGATAGTTACGCACCAACAGACGCGGAGGTTAAGGCGTACATGAACGGCTGGAAGATGTTCTCCGTGGGTGGCCCTGCTACATCAGAATATACAGGAACAGGTACAAAAGGTTGGGTTAAGATTCCGGTTAAAACTAAAAGTAATCTAGTACTAGGGACTGAATACGTTACGGATATATCAGTAACAACTCTATACAGTGACTTCCCCTACACACCGTACCAGATCCAGTACCTACTAGCGACGCCAATTGTCGAACCTGTCCAACATGAAGGCAAGCTGCTACTTAATAAAGGGTGGAACCAAATAGTGTGCGGCGGCGGTATCGAGGTTCGCGAGAAGGCGAATCCTGTCTATTGGCCCTTAGGGAACCATTGGGTATTTAACAACATACATCCTAGCCTAATTGCAGGTAGATTTAATTATAAGACTAATAAGATTTACACTGTATACGCAAACAACAAGGCAGATAGCAGTTTCGTGATGTTGAACAATGACCCCAACAGTAATGGAATAGAGGATGGGTATATAGATGATTCCAAGTATAAAAAAGATGGAACCTACCACGTCACCTATACACGCCTGGAGAACGTCGTCCCATTTCTAGCGATCGCCGGAGAGATCGCGGCGAACCTACGTGGAACGGTAGATGATTTGGTGAACGAAACGCAGGCGCTGGATACGAGGTTAAGCGTAGTTGAGCGTATGAAGGCAGAGAAGGACAGTAAAGGTACTTGGATCATGCCGACGTTATTAAATGGATGGGAGCCATACGATGTTTATAGCGGGTACGTGGCAGCATACAAGAAGGTTCCTAACACCAATCTCGTAACAATCACCGCAACTCTAAAAAACGGCTCGACCGCTTACGGAAGTACATTGTGGAATATGCCTGTCGGATATAGACCAAAGTACATTGTTTCGGGAACAGCAGTAACCCGAAATGTTGGAGTAACTGCGGTATCCGCGCTTGCTGTAGAAGTGTACACGGACGGTAGAGTGTTGTTAGGCATGAGTACAGCAGCTATTCAAAATGGCGCAATTGAGTTCTCATTGGTGTATGAAGCTGAACAATAA

Protein sequences of DBSCAN-SWA_1

>NZ_CP045294|33891:44280|34972_35407_+|WP_152397542.1|portal|DBSCAN-SWA
MATFNGEKVISGTFGEAWLDGQYIAEIMALEAKIEIEKEDVPMAGRFATDSKFMGFKGSGTLRMHKVNSRLIKALSDNLKNGVNPRFQIMSSLNDPSSGGAERITIKDASFNDLSLINWELKKKGEIEAPFTFTDWNVEDSIKP
>NZ_CP045294|33891:44280|41640_44280_+|WP_152397551.1|DBSCAN-SWA
MATTPKINLPLIDSSMTADIPRDMNALANAIDAVVETTTGAKTKVDQALASAKAYVDADLKEAPAVPINLKMGMQVIDAKETSLVNITGLKGRTLVNLLGRDGNCEDMSKWSLIGTTVLDTANKTCGMNGFKSTVTNGTYADIWRTVAYDKNKYYIALADIKNGNALKMRLRMNDNVAVKEIMSRDVTETSQFTTAWVRIEPNAFTGTNPVYLSIVTAGGNGSYGYVDAIRLYEIPKMEYEALTSMADSQIAAKYPYVDSLQNVANPYVIGYGENLLPPFMEWIPSGNLTQYSALAPYEASTVTTGDFQALISPQIPAVKGQTYTLSIESRAGRMVVGQYDKAGNVIDYPVAEAQNGQGAFSATFTVADNVSHLVVQLSNYGAGTFIFKKPILTLGSTSKPFVLRQDSILALTTELASNVDGSIADELFTKDGLYWKLSKYKKITLDGSRDWKFNAVKSGFKQVRLEGNQKASGSPVIQYATKYDGKALKYDGNVTEGDSFNVTSTNDVIYMGISNADSGWGDSYAPTDAEVKAYMNGWKMFSVGGPATSEYTGTGTKGWVKIPVKTKSNLVLGTEYVTDISVTTLYSDFPYTPYQIQYLLATPIVEPVQHEGKLLLNKGWNQIVCGGGIEVREKANPVYWPLGNHWVFNNIHPSLIAGRFNYKTNKIYTVYANNKADSSFVMLNNDPNSNGIEDGYIDDSKYKKDGTYHVTYTRLENVVPFLAIAGEIAANLRGTVDDLVNETQALDTRLSVVERMKAEKDSKGTWIMPTLLNGWEPYDVYSGYVAAYKKVPNTNLVTITATLKNGSTAYGSTLWNMPVGYRPKYIVSGTAVTRNVGVTAVSALAVEVYTDGRVLLGMSTAAIQNGAIEFSLVYEAEQ
>NZ_CP045294|33891:44280|36618_37656_+|WP_152397545.1|DBSCAN-SWA
MLGGLGKGLGGLGKMLNPFKLIGKIVPMFRLLGPVISKLSPLVAKLGDAFLKGMGKSSGIIKKVSTLIGSFQSVLINLVTMAGQRFAQFIAWLQPALPTIVGFITGVVQKAVQFFAPLLPPIMQVFQTVFGWIVENMPVFQAAIGSVFSALGPIIQTVVNVFQMLWGIWMEAWPTIQSILESVWAVVQPIFDVFITIIQILMNVIQAVWDALKPVLEMIWEALKPIIDGIGSMISAFGDGLDWVLDKVFGGGGGSGQDSAVGGASDPAKKHAAGLLTVPRDNYPALLHRNEAVLTAREANQYRNGGAGRGITINLNNPVAREEADFKKWAVILRTELESAGLNMA
>NZ_CP045294|33891:44280|37672_38305_+|WP_152397546.1|DBSCAN-SWA
MIEFWLTFNNNEESIWLHIPPPSFEIQTGLCNSTVTLHELGELMLTGKRRLKTVSLSSYFPVVDDGLGQYKSPKPPKELVKMIENWRDSQKPMRLLIFGKGLVVNEAMVIENFSYSQKNGPEDVYFTLDLKEYRFVKVKTTPLNAKEAEQLRPRPSDRGLAKTYTVQPGDTLKKIAKKVYGDESRSITIKETNHITSEYSLKVGMQLKIG
>NZ_CP045294|33891:44280|39999_41052_+|WP_152397549.1|plate|DBSCAN-SWA
MFEQQSWDSILARMLNRFAPQGVAKQEGSFVYDAMSPVAVELSQAYSDLDRVLEQGFAETSNGVYLDRRAGEHGVTRKPPAKAHGIVKVSGTAGAKIPAGAMFATKNGTLFVAAAEAVITTEGFVKVNVAAEEAGVSGNVPALGITEIIGSIPGVQQAVNEAACAGGYDGETDDALLDRLLTKVRTPATSGNANQYRQWAMEVTGIADAKVFPLWNGNGTVKVVLLDDNRRAPVPELVTQVANHIALVRPIGANVTVSAAVEVPLNIDVDLDVLPGTSLEDAKALITSEIIVYLKGLSFVDPIVRTARIANVILDTKSIVDYRDLKINGSMENIIIPEGSVAVIGTVTVR
>NZ_CP045294|33891:44280|39310_39580_+|WP_152397548.1|DBSCAN-SWA
MSELSWLVEFIRDQGQKSMGPSVLLGQVLTVPPSLVVRVQGMDLMVEDLYISSSLLLPDALRIGDRVTLMPLAGGQQFIVLSKVVKMGE
>NZ_CP045294|33891:44280|38318_39311_+|WP_152397547.1|DBSCAN-SWA
MRIVYISRTNQKSDITELFIRATWSGDVKEVARKLEVSFAVNAGEPYLPKLFMDLGEMLMVIDDEGKELWRGYIFAKSKSLSGTEVTYTAYDGLIYLTKSKVSKNFKQVTAEQITNLLCKEFGIPVGQLAKTNIPQSFVHMGKTVYEAIMTGYTLASSRTKRKYMPRMREGKLDVVLLGETVVKRILTAETDLLESTVDESIDAMVNRVLIVNEAGSVERVVDNGPWVEKYGQMQEVYQKEEGKDANQEAKSRLYGMDRSASVQVIGGRDAYDLVAGNAVRMIEDVTGMTGLFYIENDSHSFENGVHTLNLQLNFEKVMDEYMPDEQGGI
>NZ_CP045294|33891:44280|35437_35860_+|WP_152397543.1|DBSCAN-SWA
MSQLSLDLLLKMDKSKIQRPTAKIEMSRLSELVGEPVIFTCQALTMDEFEEVQEVSVSFGKKGELEEFSTNKVQIFTLLKGIVDPKLSDSKLLEAYGVTTPKQLIEESKLLLPGEVTQLYNVISSLSGFGDEAVKELKNG
>NZ_CP045294|33891:44280|41048_41639_+|WP_152397550.1|DBSCAN-SWA
MTDVRERAVIERAVGNNPLRRYVPEFVSGSRILGGMLDSQYQENQELTASIDEVLDQFYIETATWGLDRWERMCGIATDPSKPLDQRRSVIKSKLRGIGTVTVDLVKNVAEAFANGQVDVQEDVAKYTITVTFVGKLGIPPNMEDITHALRDIIPAHLGIEYVYKFYPYYELAKSGKKYQDLTSLTYYKLVDKGVQ
>NZ_CP045294|33891:44280|39590_40007_+|WP_152397553.1|DBSCAN-SWA
MVDVPPDIAVGVGSGASLPLFREYAWDFDRDEFVMKDGQLVLLEGQAAVQVWVYKALRTERYRYLAYTWDYGNEIERLIGSTFSPAAQRSEAERYVREALMVLPYIREVNQIEIASEGDELRIEATVETVYGEVKVRV
>NZ_CP045294|33891:44280|36224_36659_-|WP_152397544.1|DBSCAN-SWA
MPRPPSPLPNPPSNPPKPPSRPPPLPPFPPRLPPLLFLLGGSPPSSPLGYFGPTGGGFISVAFVRFGFIFSIEYLILNSALPPNFLIAILSATSVAMKIPAFISISFQSNLIFGSATSSMLNFAVPSICAFISSICLRTTFVFT
>NZ_CP045294|33891:44280|33891_34959_+|WP_152397541.1|tail|DBSCAN-SWA
MGLPNVNIIFKQKAASAVQQGAVGVVAIVLKDASVSALTSYELHGADESPQALKAQNAAYVQQAFMGMPKLVKLVVIPETETDYSKAMQYLETIAFNVVAFPGAATADVTALSTWAKNVFTNKDRKIIAVLPNSAADHPSVVNLATDNIEVGAQKYTATQYTARIAGLIAGLPLTVAPTFQVLPEVTNVPSMTKSEADTAVNAGKFVLYHDGEKVKIARGVTSLVTTTEAMGEDWKKIKVVRILNKTYQDLKETVEDFYVGKVQNSYMNKLLLISAMNAYYESLEQDGILDPGKNAAEIDLAAQRTYLKSILGTEVVAGMTDQQVKEANTRDKVFIMARQRPLDAIEDVTMTVYL

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_152397541.1|33891_34959_+|tail	phage tail sheath protein	A0A0A7S0D2	Clostridium_phage	2.6e-57	38.2
WP_152397542.1|34972_35407_+|portal	phage portal protein	A0A1V0DZX1	Clostridioides_phage	2.0e-27	45.6
WP_152397543.1|35437_35860_+	XkdN-like protein	NA	NA	NA	NA
WP_152397544.1|36224_36659_-	hypothetical protein	NA	NA	NA	NA
WP_152397545.1|36618_37656_+	hypothetical protein	NA	NA	NA	NA
WP_152397546.1|37672_38305_+	LysM peptidoglycan-binding domain-containing protein	J9QDY6	Clostridium_phage	4.9e-19	31.6
WP_152397547.1|38318_39311_+	hypothetical protein	A0A0K2SUC1	Clostridium_phage	5.7e-30	30.9
WP_152397548.1|39310_39580_+	hypothetical protein	NA	NA	NA	NA
WP_152397553.1|39590_40007_+	DUF2634 domain-containing protein	A0A1V0DZX2	Clostridioides_phage	5.0e-28	42.3
WP_152397549.1|39999_41052_+|plate	baseplate J protein	S6AVU3	Thermus_phage	2.0e-57	39.9
WP_152397550.1|41048_41639_+	DUF2313 domain-containing protein	S6BFJ0	Thermus_phage	2.4e-28	40.1
WP_152397551.1|41640_44280_+	hypothetical protein	A0A0K2D0A9	Bacillus_phage	1.7e-17	31.9