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_CP017704	Bacillus simplex NBRC 15720 = DSM 1321, complete genome	3 crisprs	DEDDh,RT,csa3,cas14j,DinG,cas3	0	2	2	0

1. NZ_CP017704

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP017704_1

• CRISPR_ID: NZ_CP017704_1
• CRISPR_location: 1334243-1334328
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP017704_1

Consensus_repeat	Method
CGGTGACCAGCATAAGACAGAGGAAATCG	CRISPRCasFinder

spacers of NZ_CP017704_1

>1.1|1334272|28|NZ_CP017704|CRISPRCasFinder
TTGAAAAAGCTCTCCACTCTGAGCATGG

CRISPR arrays and Neighbor proteins around NZ_CP017704_1

CRISPR arrays

The CRISPR arrays of NZ_CP017704_1

>merge|NZ_CP017704|1|1334243-1334328|CRISPRCasFinder
CGGTGACCAGCATAAGACAGAGGAAATCGTTGAAAAAGCTCTCCACTCTGAGCATGGCGGTGACCAGCAAAAGACAGAGGAAATCG

>NZ_CP017704|1|1|1334243-1334328|CRISPRCasFinder
CGGTGACCAGCATAAGACAGAGGAAATCG	TTGAAAAAGCTCTCCACTCTGAGCATGG
CGGTGACCAGCAAAAGACAGAGGAAATCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017704.1|WP_063232210.1|1335857_1336724_+|DegV-family-protein	unknown	unknown	gnl|CDD|273257
NZ_CP017704.1|WP_063232212.1|1337754_1338630_+|glucose-1-dehydrogenase	unknown	unknown	gnl|CDD|187613
NZ_CP017704.1|WP_063232204.1|1329589_1330279_+|Crp/Fnr-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223736
NZ_CP017704.1|WP_063232202.1|1327070_1328303_-|bifunctional-ornithine-acetyltransferase/N-acetylglutamate-synthase	unknown	unknown	gnl|CDD|235441
NZ_CP017704.1|WP_063232200.1|1325137_1326289_-|acetylornithine-transaminase	unknown	unknown	gnl|CDD|179505
NZ_CP017704.1|WP_063232211.1|1337027_1337519_+|YajQ-family-cyclic-di-GMP-binding-protein	unknown	unknown	gnl|CDD|213038
NZ_CP017704.1|WP_063232205.1|1330536_1331550_-|GTP-3',8-cyclase-MoaA	unknown	unknown	gnl|CDD|234672
NZ_CP017704.1|WP_063232209.1|1334858_1335701_-|YitT-family-protein	unknown	unknown	gnl|CDD|224203
NZ_CP017704.1|WP_063232203.1|1328319_1329357_-|N-acetyl-gamma-glutamyl-phosphate-reductase	unknown	unknown	gnl|CDD|234761
NZ_CP017704.1|WP_063232411.1|1332085_1332874_-|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|182555
NZ_CP017704.1|WP_063232199.1|1323972_1325055_-|carbamoyl-phosphate-synthase-small-subunit	unknown	unknown	gnl|CDD|183784
NZ_CP017704.1|WP_063232214.1|1339563_1340607_-|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|380517
NZ_CP017704.1|WP_072272565.1|1336792_1336924_+|DUF3941-domain-containing-protein	unknown	unknown	unknown
NZ_CP017704.1|WP_063232207.1|1333105_1333921_+|Cof-type-HAD-IIB-family-hydrolase	unknown	unknown	gnl|CDD|319818
NZ_CP017704.1|WP_063232206.1|1331658_1331967_-|metal-sulfur-cluster-assembly-factor	unknown	unknown	gnl|CDD|225062
NZ_CP017704.1|WP_063232213.1|1338724_1339525_+|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|293798
NZ_CP017704.1|WP_063232215.1|1340949_1342599_-|alpha-glucosidase	unknown	unknown	gnl|CDD|200472
NZ_CP017704.1|WP_053534119.1|1334470_1334722_-|general-stress-protein	unknown	unknown	gnl|CDD|226252
NZ_CP017704.1|WP_063232201.1|1326285_1327059_-|acetylglutamate-kinase	unknown	unknown	gnl|CDD|234869
NZ_CP017704.1|WP_063232216.1|1342678_1344214_-|alpha-amylase	unknown	unknown	gnl|CDD|200478

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP017704.1|WP_063232210.1|1335857_1336724_+|DegV-family-protein	gnl|CDD|273257	TIGR00762, DegV, EDD domain protein, DegV family. This family of proteins is related to DegV of Bacillus subtilis and includes paralogous sets in several species (B. subtilis, Deinococcus radiodurans, Mycoplasma pneumoniae) that are closer in percent identity to each than to most homologs from other species. This suggests both recent paralogy and diversity of function. DegV itself is encoded immediately downstream of DegU, a transcriptional regulator of degradation, but is itself uncharacterized. Crystallography suggested a lipid-binding site, while comparison of the crystal structure to dihydroxyacetone kinase and to a mannose transporter EIIA domain suggests a conserved domain, EDD, with phosphotransferase activity. [Unknown function, General].	2.08829e-119
NZ_CP017704.1|WP_063232212.1|1337754_1338630_+|glucose-1-dehydrogenase	gnl|CDD|187613	cd05355, SDR_c1, classical (c) SDR, subgroup 1. These proteins are members of the classical SDR family, with a canonical active site tetrad and a typical Gly-rich NAD-binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	2.8463e-173
NZ_CP017704.1|WP_063232204.1|1329589_1330279_+|Crp/Fnr-family-transcriptional-regulator	gnl|CDD|223736	COG0664, Crp, cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases [Signal transduction mechanisms].	1.02302e-46
NZ_CP017704.1|WP_063232202.1|1327070_1328303_-|bifunctional-ornithine-acetyltransferase/N-acetylglutamate-synthase	gnl|CDD|235441	PRK05388, argJ, bifunctional glutamate N-acetyltransferase/amino-acid acetyltransferase ArgJ.	0
NZ_CP017704.1|WP_063232200.1|1325137_1326289_-|acetylornithine-transaminase	gnl|CDD|179505	PRK02936, argD, acetylornithine transaminase.	0
NZ_CP017704.1|WP_063232211.1|1337027_1337519_+|YajQ-family-cyclic-di-GMP-binding-protein	gnl|CDD|213038	cd11740, YajQ_like, Proteins similar to Escherichia coli YajQ. In Pseudomonas syringae, YajQ functions as a host protein involved in the temporal control of bacteriophage Phi6 gene transcription. It has been shown to bind to the phage's major structural core protein P1, most likely activating transcription by acting indirectly on the RNA polymerase. YajQ may remain bound to the phage particles throughout the infection period. Earlier, YajQ was characterized as a putative nucleic acid-binding protein based on the similarity of its (ferredoxin-like) three-dimensional topology with that of RNP-like RNA-binding domains.	6.15959e-82
NZ_CP017704.1|WP_063232205.1|1330536_1331550_-|GTP-3',8-cyclase-MoaA	gnl|CDD|234672	PRK00164, moaA, GTP 3',8-cyclase MoaA.	4.65458e-154
NZ_CP017704.1|WP_063232209.1|1334858_1335701_-|YitT-family-protein	gnl|CDD|224203	COG1284, COG1284, Uncharacterized conserved protein [Function unknown].	2.77471e-76
NZ_CP017704.1|WP_063232203.1|1328319_1329357_-|N-acetyl-gamma-glutamyl-phosphate-reductase	gnl|CDD|234761	PRK00436, argC, N-acetyl-gamma-glutamyl-phosphate reductase; Validated.	0
NZ_CP017704.1|WP_063232411.1|1332085_1332874_-|alpha/beta-fold-hydrolase	gnl|CDD|182555	PRK10566, PRK10566, esterase; Provisional.	7.09815e-56
NZ_CP017704.1|WP_063232199.1|1323972_1325055_-|carbamoyl-phosphate-synthase-small-subunit	gnl|CDD|183784	PRK12838, PRK12838, carbamoyl phosphate synthase small subunit; Reviewed.	0
NZ_CP017704.1|WP_063232214.1|1339563_1340607_-|LacI-family-DNA-binding-transcriptional-regulator	gnl|CDD|380517	cd06294, PBP1_MalR-like, ligand-binding domain of maltose transcription regulator MalR which is a member of the LacI-GalR family repressors. This group includes the ligand-binding domain of maltose transcription regulator MalR which is a member of the LacI-GalR family repressors that are composed of two functional domains: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal ligand-binding domain, which is homologous to the sugar-binding domain of ABC-type transport systems that contain the type 1 periplasmic binding protein-like fold. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcription repressor undergoes a conformational change upon ligand binding which in turn changes the DNA binding affinity of the repressor.	1.77658e-113
NZ_CP017704.1|WP_063232207.1|1333105_1333921_+|Cof-type-HAD-IIB-family-hydrolase	gnl|CDD|319818	cd07516, HAD_Pase, phosphatase, similar to Escherichia coli Cof and Thermotoga maritima TM0651; belongs to the haloacid dehalogenase-like superfamily. Escherichia coli Cof is involved in the hydrolysis of HMP-PP (4-amino-2-methyl-5-hydroxymethylpyrimidine pyrophosphate, an intermediate in thiamin biosynthesis), Cof also has phosphatase activity against the coenzymes pyridoxal phosphate (PLP) and FMN. Thermotoga maritima TM0651 acts as a phosphatase with a phosphorylated carbohydrate molecule as a possible substrate. Escherichia coli YbhA is also a member of this family and catalyzes the dephosphorylation of PLP, YbhA can also hydrolyze erythrose-4-phosphate and fructose-1,6-bis-phosphate. Members of this family belong 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.	3.40803e-76
NZ_CP017704.1|WP_063232206.1|1331658_1331967_-|metal-sulfur-cluster-assembly-factor	gnl|CDD|225062	COG2151, PaaD, Predicted metal-sulfur cluster biosynthetic enzyme [General function prediction only].	1.10738e-39
NZ_CP017704.1|WP_063232213.1|1338724_1339525_+|MBL-fold-metallo-hydrolase	gnl|CDD|293798	cd07712, MBLAC2-like_MBL-fold, uncharacterized human metallo-beta-lactamase domain-containing protein 2 and related proteins; MBL-fold metallo hydrolase domain. Includes the MBL-fold metallo hydrolase domain of uncharacterized human MBLAC2 and related proteins. Members of this subgroup belong to the MBL-fold metallo-hydrolase superfamily which is comprised mainly of hydrolytic enzymes which carry out a variety of biological functions.	3.83414e-56
NZ_CP017704.1|WP_063232215.1|1340949_1342599_-|alpha-glucosidase	gnl|CDD|200472	cd11333, AmyAc_SI_OligoGlu_DGase, Alpha amylase catalytic domain found in Sucrose isomerases, oligo-1,6-glucosidase (also called isomaltase; sucrase-isomaltase; alpha-limit dextrinase), dextran glucosidase (also called glucan 1,6-alpha-glucosidase), and related proteins. The sucrose isomerases (SIs) Isomaltulose synthase (EC 5.4.99.11) and Trehalose synthase (EC 5.4.99.16) catalyze the isomerization of sucrose and maltose to produce isomaltulose and trehalulose, respectively. Oligo-1,6-glucosidase (EC 3.2.1.10) hydrolyzes the alpha-1,6-glucosidic linkage of isomaltooligosaccharides, pannose, and dextran. Unlike alpha-1,4-glucosidases (EC 3.2.1.20), it fails to hydrolyze the alpha-1,4-glucosidic bonds of maltosaccharides. Dextran glucosidase (DGase, EC 3.2.1.70) hydrolyzes alpha-1,6-glucosidic linkages at the non-reducing end of panose, isomaltooligosaccharides and dextran to produce alpha-glucose.The common reaction chemistry of the alpha-amylase family enzymes is based on a two-step acid catalytic mechanism that requires two critical carboxylates: one acting as a general acid/base (Glu) and the other as a nucleophile (Asp). Both hydrolysis and transglycosylation proceed via the nucleophilic substitution reaction between the anomeric carbon, C1 and a nucleophile. Both enzymes contain the three catalytic residues (Asp, Glu and Asp) common to the alpha-amylase family as well as two histidine residues which are predicted to be critical to binding the glucose residue adjacent to the scissile bond in the substrates. The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase.	0
NZ_CP017704.1|WP_053534119.1|1334470_1334722_-|general-stress-protein	gnl|CDD|226252	COG3729, GsiB, General stress protein [General function prediction only].	4.48002e-05
NZ_CP017704.1|WP_063232201.1|1326285_1327059_-|acetylglutamate-kinase	gnl|CDD|234869	PRK00942, PRK00942, acetylglutamate kinase; Provisional.	1.5226e-89
NZ_CP017704.1|WP_063232216.1|1342678_1344214_-|alpha-amylase	gnl|CDD|200478	cd11339, AmyAc_bac_CMD_like_2, Alpha amylase catalytic domain found in bacterial cyclomaltodextrinases and related proteins. Cyclomaltodextrinase (CDase; EC3.2.1.54), neopullulanase (NPase; EC 3.2.1.135), and maltogenic amylase (MA; EC 3.2.1.133) catalyze the hydrolysis of alpha-(1,4) glycosidic linkages on a number of substrates including cyclomaltodextrins (CDs), pullulan, and starch. These enzymes hydrolyze CDs and starch to maltose and pullulan to panose by cleavage of alpha-1,4 glycosidic bonds whereas alpha-amylases essentially lack activity on CDs and pullulan. They also catalyze transglycosylation of oligosaccharides to the C3-, C4- or C6-hydroxyl groups of various acceptor sugar molecules. Since these proteins are nearly indistinguishable from each other, they are referred to as cyclomaltodextrinases (CMDs). This group of CMDs is bacterial. The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues (Asp, Glu and Asp) performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase.	2.5246e-86

Protein sequences

>NZ_CP017704.1|WP_063232207.1|1333105_1333921_+|Cof-type-HAD-IIB-family-hydrolase
MAEKHLIVLDLDGTLLTDNKTISSRTKKTLLKLKEDGHEVMIATGRPFRSSELYYRELGLTTPIVNFNGAFVHHPLHTSWGVYHSPLDISVAKDIVEACDQFKYHNIIAEVRDDVYVHYHDEKLMNMFNVGNPNMKTGDLRNYLQDSPTSMLIHTDSEFVGQIRQHLSDVHAELVDHRRWAEPFHIIEIIKSGLSKAVGLKRVSNYLEIPQNRIIAFGDEDNDLEMLDYAGTGVAMGNAISPVKTVANATTLTNEEDGIAVFLEEKFNIKA
>NZ_CP017704.1|WP_063232411.1|1332085_1332874_-|alpha/beta-fold-hydrolase
MIIIEKEHIGHIPVLHLGKEATFNQELPLIIFIHGFQSAKEHNLHYAYLLAEKGFRVLLPDVIHHGERGAGLSDSQMMPRFWEMVLQTIQDLSLLKDDLLSRKLIDPDRIGVAGTSMGGIVTNGALAAYEWICAGVSLMGNPSYVAYAELQMAEIKKRKVKFPATDEEVAKVIEQLKPFDLSLNQDKLSNRPLLFWHGAKDPVVPYQHAYRFYEGVKAGYKEADEKIDFILDPKAGHKVSREGVLMTADWFAKHLLSTVQNA
>NZ_CP017704.1|WP_063232206.1|1331658_1331967_-|metal-sulfur-cluster-assembly-factor
MDQDTKDIIIGALEQVIDPELGIDIVNLGLVYDVDMDEEGLTTVTMTLTAMGCPMAGTIVDQVKLVLEDIPEVKETDVKIVWSPPWTKDKMSRYAKIALGIK
>NZ_CP017704.1|WP_063232205.1|1330536_1331550_-|GTP-3',8-cyclase-MoaA
MNSQIKDSLDRPLRDLRISVIDRCNFRCQYCMPAEIFHENFQFLPKSELLSYEEIVRLSEIFASLGVKKLRLTGGEPLLRRDLTTLISNLVKIDGIEDIGLTTNGVFLKKHAANLRAAGLQRVNISLDSLDDELFKKMNGRDIGIKPVIEGIAAAKEAGLGVKVNMVVKKETNESQILPMARFCKDEGIQLRYIEFMDVGHTNGWQLKNVITKKELLAMLQTEFDLEPVEEDYFGEVAKRFRYKGTTAEVGFITSVSESFCSSCTRARLSANGSLYTCLFNGKGHDLKSLLRSDMTDEELTGFIISLWNRRDDRYSDERAAGTVKKQEKIEMSFIGG
>NZ_CP017704.1|WP_063232204.1|1329589_1330279_+|Crp/Fnr-family-transcriptional-regulator
MNELSLTNRMHAILDNKHQVKHMEKGRYLFQESTPASDLYYIIKGKVEVSKVVPDGRELTIRISSENDLVGETVLFSQNPKYMMNAKMMEDGTVAVISKEALEDKIASDSRLAVDMMTWLSAQNRKNQAKFRDMLLHGKKGAFYSTLIRLSNSYGTEVEDGKVINLPFTNQELANFCGTSREVVNRMLAQLRKNNVISIKKGRITILDFDYLKQEIDCENCPIDICTID
>NZ_CP017704.1|WP_063232203.1|1328319_1329357_-|N-acetyl-gamma-glutamyl-phosphate-reductase
MNVSLVGATGYGGLELIRFLNNHPQFKIKSLHTSSQFGRSLYEENAHLMHMKDKLEEIDPEAIAKKSDIVFLATPSGVSSQLISEFSDLDIKVIDLSGDLRLQTPGEYEHWYKKPAAPQQIIEEAVYGLAEWNAEAIKKATIIANPGCYPTASLLGLAPLFTEGLAGAAADVIIDAKSGVSGAGKSPSAVTHYSEMNENFKIYKVNQHQHIPEIEQQLGRWSSGLQPITFNTHLVPMTRGIMATMYIKVNRETSNVELKDLYETVYENHPFVRVQPLDRFPSTKQVYGSNFCDIGVDYDERTGKVTVVSVIDNLVKGAAGQAIQNANILMGLEETAGLWNSPLYP
>NZ_CP017704.1|WP_063232202.1|1327070_1328303_-|bifunctional-ornithine-acetyltransferase/N-acetylglutamate-synthase
MNTLQPVEVIKQIQEGNILMPQGFKASGVHAGLRYSKKDVGIIFTDVPASAAAVYTQNVVQAAPINVTKDSIAVTGKLHGIVVNSACANACTGEQGLKDANEMRKLAAQKFGLEDHSFAVASTGVIGEFMEMEKVRKGIESLQPENTPEAAEAFGTAILTTDIVTKSCGYETIIDGKTVKMGGAAKGSGMIHPNMATMLGFITTDAVIEPDDLQQALSSITNDTFNQITVDGDCSTNDMVLVLANGEANNDPLTPNHPEWSIFLELLKQTSENLAKQIAKDGEGATKLIEVNVHGMHTKQDSQMMAKTIVGSNLVKTAAFGADANWGRIIAAMGRSGVAFNPDQTTIVFGDIVVLNDGEPIMFSEEEAKAYLENESIIIHVYLKDGNESGTAWGCDLTYDYVKINGSYRS
>NZ_CP017704.1|WP_063232201.1|1326285_1327059_-|acetylglutamate-kinase
MDILVIKCGGSIINELSESFFNSVRELQNRGYHIVFVHGGGPDINSMLEKFEIEPVFEDGLRKTTTEVLEIVELMLAGKSNRSLVHKLEAHGIKAIGINGSDGGILTGDYIDKQKLGAVGEIQQVNTELFGLLFEKGYCPVLTPISTTEEGTKLNVNADMAAGSVAKALSADMCLFVTDVKGVLKNGQIIEKLNETETKNMIMDGSIHGGMIPKVNTALSVLNKGIEEVMIVSGKDHFYQGGQFIGTKFLQEEGVFQ
>NZ_CP017704.1|WP_063232200.1|1325137_1326289_-|acetylornithine-transaminase
MSSLFPTYARWNIEPDTASGLKITSATGKEYLDFTSGIGVLNLGHCHEKVKMAVTEQLNKYWHVSNMFQSSIQERTAKMLADASGLSQVFFANSGAEANEAAIKLARKATGKSKIITCQQSFHGRTFATMAATGQEKIKTGFGPMLASFEYVPFNDNDAMTAAIDENTAAVMIEIVQGEGGIHVVQQSYLDVIQTQCQEHGALLIIDEIQTGIGRTGKPFAFQHFNIQPDIITSAKGLGNGLPIGAMIGKEALSEFFNPGSHGSTFGGNPVSVSAAEAVLKEIFQSGFLKETVKKAEYLESELAKALKDMEEVKEIRGLGMMVGIECKQDVQAFLMELQEEGLLVLSAGPKVLRLLPSLTVTESEINSAINKIKKVLAIKQTV
>NZ_CP017704.1|WP_063232199.1|1323972_1325055_-|carbamoyl-phosphate-synthase-small-subunit
MKSYLYLENGSVFEGELLTKSTEKTITGEIVFFTGMTGYQEVLTDPSYKDQIVIFTYPLIGNYGINEHDFESKKPHVAGVIVYEGNMSHSHYQAKYSLGEYLDKWNIPLLSHVDTRAVVKNIRQEGSMQAVITAEEKYTVVPGLNGLSAHVAEVSTKIVESFGKGDKHVVMMDFGYKKSILDSLVEQGCRVSVVPFDTEFEQIKDLKPDGILLSNGPGDPKQLEYLLGNIKKIITNFPTMGICLGHQLTALALGGNTKKMLFGHRGANQPVVDLKTKKVYMSSQNHSYEVDEPSLQGTSLQVRFRNVNDNTVEGLMHEDLPIFTTQYHPEANPGPIESSLLFNDFLQMINDYSGREKAYA
>NZ_CP017704.1|WP_053534119.1|1334470_1334722_-|general-stress-protein
MANDEKMSRQEAGRKGGEATSKNHDKDFYREIGQKGGEATSDNHDKEFYQEIGQKGGEATADSHGKDFYKEIGEKGGKARNNN
>NZ_CP017704.1|WP_063232209.1|1334858_1335701_-|YitT-family-protein
MYSGEMKKIIIVVVGALLNAIAMNFFLIPANVYASGFTGVAQLLSRMIGSFAPFNVSTGILLLLLNIPVTIIAWRKVGKSFTFYSFLSVVLMSFFMEIIPITRWSPDILLNAVFGGVIAAVGVGITLKYGASTGGMDIIAMLLSRKKDKPVGTYLFLLNGVIIVTAGAVYGPEKALYTLVTLYTSTRVVDAIHTRHEKLTAMIITKKSEELKQAIHAQLVRGITRVPAKGAFTNETKEMLLIVITRYELYDLERIIKEVDPHAFTNIIETSGIVGTFRRE
>NZ_CP017704.1|WP_063232210.1|1335857_1336724_+|DegV-family-protein
MAITILADSACDLPLSFYKENNVSLIPLQVHLDGENYEDLLTINSHEVYQAMLEGKAPKTSQASPEYFIETFTQFAKEKKQGIYIAFSSELSGTYQTAVMILNQVKEEYPDLDIEIVNTKCASMGVGLIVKKAADLAANGATKEEILADIEFQTRHMEHLFTVDNLEYLARGGRISKTSALVGGLLNIKPLLHVEDGKLVPLEKIRGKKKLIKRVIELMHERGKNLTTQTIAISHGDDEATALEWKEAIQNEFGTTDFMIHTIGSVIGAHAGPGTIALFFLNDTPEKS
>NZ_CP017704.1|WP_072272565.1|1336792_1336924_+|DUF3941-domain-containing-protein
MSKTTDDNKRPKDNQARNAEKNIAYQENLAAGKHSYSKKTDHK
>NZ_CP017704.1|WP_063232211.1|1337027_1337519_+|YajQ-family-cyclic-di-GMP-binding-protein
MAKENSFDIVSKVDFSEVTNAVTMAMKEIQTRYDFKGSISSITIEKEDLVLVSDDEYKLEQLKDVLISKLIKRDVPVKNLDYGKLEGASGGTVRQRAKLIQGIDKEQAKKINTIIKNSGLKVKSQIQDDQIRVTGKNRDDLQGIISAIRGADLSIDVQFLNYR
>NZ_CP017704.1|WP_063232212.1|1337754_1338630_+|glucose-1-dehydrogenase
MTTQNQNQNKQGFPPQHQQHQPGLETKMEPNPDSVKAAYKGSGKLKGKTAIITGGDSGIGKSVAIYYAKEGANVTVAYLDEHEDAKTTKELIEKEGQKCLLISGDIGDEAFCQDVVKKTVDEFGGLDILVNNAGEQHVQTSILDISAEQLEKTFRTNIFSMFHLTKAALKHLKKGSSIINTTSITAYQGNPKLIDYSSTKGAILAFTRALSNSISKDGIRVNGVAPGPIWTPLIPASFGEADVAKFGQDTPMGRAGQPEELAPAYVYLASDDSSYVSGQVIHVNGGTVVNG
>NZ_CP017704.1|WP_063232213.1|1338724_1339525_+|MBL-fold-metallo-hydrolase
MESFLENIVDPWFTVQELDSKTFAISEYGHWEKVHSFLLLGETRAALIDTGLGICSIKRITDQLTNLPIIVLTTHVHADHIGGHGDYDTIYVHGDDANWLINGIEGLSLEQIRKNMARDITVPIPESFDPFTYNPYQGYPDRLLSDGDTIDLGNRSLNIYHTPGHSPGHISILDNETGYLFTGDLLYSDTPVYAFYPSTSPEDLVNSLEKIAKIKAVSKIYGGHNQLGLEPRILEEVLAAIQYLKENNLVRHGTGVHAFKSFSVHF
>NZ_CP017704.1|WP_063232214.1|1339563_1340607_-|LacI-family-DNA-binding-transcriptional-regulator
MAITIKDVAQLANVAPSTVSRVIANNPRISEKTKVRVRKAMSKLGYHPNFIARSLANQSTRIIGLVMPSSSNDYYQNPFFSTILQGLSEGAQENHYSLLLSTGKTEDEIYEGVVNMVQGGMVDGIILMYSRMNDHILTYLRARAFPFVIIGKPFDFIEEITYVDNDNVLAAEQATDYLIQLGHERIGFIGGDVTLVMTLDRLSGYERALKRAGIDRRREYTLHEDFLHEGGQAAAKRLLSIDEPPTALVVSDDLMALGIVHSLREMGVRTPEEMSIVSFNNVVFSELSLPALTSVDINIFDLGYQAAKGIIHMLQTGDTPAGTIIPHHFVERHSCRSIKQGAMAMTY
>NZ_CP017704.1|WP_063232215.1|1340949_1342599_-|alpha-glucosidase
MNKTWWKEAVCYQIYPRSFMDSNGDGVGDIKGLISKLDYLQELGIDVIWICPFYKSPNADNGYDISDYQAVSDEFGSIEDIDLLLKDVHGRGMKVILDLVLNHTSDEHPWFVESRSSRDNPKRDWYIWRDGQDGREPNNWESIFSGSAWKFDERTNQYYLHLFAEKQPDLNWKNTDVRQALYEMVNWWLDKGIDGFRIDAITHIHKREGLPDMPNPYWHQYVPAFEMHTNQDGILDYLQELKEETFSKYDIMTVGEANGVRIEQAEEWVGESNGKFNMIFQFEHLGLWNRGQNHAVDVQGLKRTMTKWQKGLKNKGWNALFFENHDQPRSVSTWGNDHQYWLESAKMIGALYFFMQGTPFIYQGQEIGMTNVQFDSIDDYDDVGMKNFYRIETSKGRPHDEIMNIIWHSGRDNSRTPMQWNDIENGGFTHGTPWMRVNPNYRAINVEQQKNDPLSIYHFYKKMIELRKKHQVLVYGEYELLWEDHPELYIYTRSMNDNSVMVVCNFSMNHHQIDLSYWGEMELLLANYEDCPEVSFIDLRPYETRVYRY
>NZ_CP017704.1|WP_063232216.1|1342678_1344214_-|alpha-amylase
MRKRVLSLALIPLLLFYAIPVGAAEKEQRTWKDEIVYSLLVDRFFDGNTQNNGDANVNDPSTFNGGDFEGVTKKLNYLKDMGYTAIILSPIFANDENGYHGDWVADFYKTDKHYGTMKEFKKLVNEAHKRDMKVIIDFQANNVGPDSTWLTDPKKQDWFHEEKKISKEGSQTDLETGWVDGLPDLNQDNEETREYLLDAAKWWITETDIDGYRINKVQYVAKDFWKEFVDAVKSEKSNFYTIGDVQGDADLISSYKKTGIDAFMAYPQNAELREAFAAPDKELKPIFNAFAKSEDELGGNAHQALFMDTQGMPRFTKDAADHNENPGTRWRMALSYLYTMPGVPIVFYGSEIALNGDIAPDNHKLMNFKTEQELVEYITKLSDLRDMYPALVKGDMELLYEKVGTSVFKRVYGDETIVVAMNNTTKTQTINLTDKELESNKELRGMLNGDLVRSKDNSYSIVIDRETTEVYTLSPKSIINIPYLLVIGLVLLIFGIFIALVIKRSKRNQPK

Crispr_ID: NZ_CP017704_2

• CRISPR_ID: NZ_CP017704_2
• CRISPR_location: 1389026-1389145
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP017704_2

Consensus_repeat	Method
TGATTCACATCATAATGTAAATGAGGTGTCAGTTAAAGACGTAT	CRISPRCasFinder

spacers of NZ_CP017704_2

>2.1|1389070|32|NZ_CP017704|CRISPRCasFinder
TACACTGAAATACCCATAAGTTTTATTACAAA

CRISPR arrays and Neighbor proteins around NZ_CP017704_2

CRISPR arrays

The CRISPR arrays of NZ_CP017704_2

>merge|NZ_CP017704|2|1389026-1389145|CRISPRCasFinder
TGATTCACATCATAATGTAAATGAGGTGTCAGTTAAAGACGTATTACACTGAAATACCCATAAGTTTTATTACAAATGATTCACATCATATTGTAAATGAGGTGTCAGTTAAAGACGTAT

>NZ_CP017704|2|2|1389026-1389145|CRISPRCasFinder
TGATTCACATCATAATGTAAATGAGGTGTCAGTTAAAGACGTAT	TACACTGAAATACCCATAAGTTTTATTACAAA
TGATTCACATCATATTGTAAATGAGGTGTCAGTTAAAGACGTAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017704.1|WP_034314691.1|1393113_1393692_+|HTH-type-transcriptional-regulator-Hpr	unknown	unknown	gnl|CDD|237501
NZ_CP017704.1|WP_063232252.1|1384865_1386077_+|amidohydrolase	unknown	unknown	gnl|CDD|349941
NZ_CP017704.1|WP_063232259.1|1393694_1394021_-|DUF1878-family-protein	unknown	unknown	gnl|CDD|370213
NZ_CP017704.1|WP_063232248.1|1381120_1382056_-|ferrochelatase	unknown	unknown	gnl|CDD|183526
NZ_CP017704.1|WP_061462016.1|1395206_1395290_-|YjcZ-family-sporulation-protein	unknown	unknown	unknown
NZ_CP017704.1|WP_065310849.1|1379969_1380098_+|YhfH-family-protein	unknown	unknown	gnl|CDD|379490
NZ_CP017704.1|WP_063232258.1|1392562_1392925_+|YtxH-domain-containing-protein	unknown	unknown	gnl|CDD|227313
NZ_CP017704.1|WP_063232254.1|1389521_1389944_+|HIT-family-protein	unknown	unknown	gnl|CDD|238608
NZ_CP017704.1|WP_034314696.1|1394911_1395094_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP017704.1|WP_063232249.1|1382134_1383178_-|uroporphyrinogen-decarboxylase	unknown	unknown	gnl|CDD|234644
NZ_CP017704.1|WP_063232253.1|1386916_1388125_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|377581
NZ_CP017704.1|WP_063232256.1|1391447_1391966_+|tryptophan-transporter	unknown	unknown	gnl|CDD|293704
NZ_CP017704.1|WP_063232247.1|1380261_1380837_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP017704.1|WP_063232255.1|1390217_1391321_+|3-phosphoserine/phosphohydroxythreonine-transaminase	unknown	unknown	gnl|CDD|235428
NZ_CP017704.1|WP_063232251.1|1384149_1384773_-|phosphatase-PAP2-family-protein	unknown	unknown	gnl|CDD|239486
NZ_CP017704.1|WP_063232260.1|1394263_1394803_+|DUF3267-domain-containing-protein	unknown	unknown	gnl|CDD|378690
NZ_CP017704.1|WP_063232413.1|1386106_1386811_-|EcsC-family-protein	unknown	unknown	gnl|CDD|378945
NZ_CP017704.1|WP_063232250.1|1383449_1383965_+|antibiotic-biosynthesis-monooxygenase	unknown	unknown	gnl|CDD|225209
NZ_CP017704.1|WP_081112840.1|1395473_1395557_-|YjcZ-family-sporulation-protein	unknown	unknown	unknown
NZ_CP017704.1|WP_048677969.1|1388117_1388861_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224054

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP017704.1|WP_034314691.1|1393113_1393692_+|HTH-type-transcriptional-regulator-Hpr	gnl|CDD|237501	PRK13777, PRK13777, HTH-type transcriptional regulator Hpr.	1.10378e-121
NZ_CP017704.1|WP_063232252.1|1384865_1386077_+|amidohydrolase	gnl|CDD|349941	cd08021, M20_Acy1_YhaA-like, M20 Peptidase aminoacylase 1 subfamily, includes Bacillus subtilis YhaA and Staphylococcus aureus amidohydrolase, SACOL0085. Peptidase M20 family, uncharacterized subfamily of bacterial proteins predicted as putative amidohydrolases or hippurate hydrolases. These are a class of zinc binding homodimeric enzymes involved in hydrolysis of N-acetylated proteins. N-terminal acetylation of proteins is a widespread and highly conserved process that is involved in protection and stability of proteins. Several types of aminoacylases can be distinguished on the basis of substrate specificity. Aminoacylase 1 (ACY1) breaks down cytosolic aliphatic N-acyl-alpha-amino acids (except L-aspartate), especially N-acetyl-methionine and acetyl-glutamate into L-amino acids and an acyl group. However, ACY1 can also catalyze the reverse reaction, the synthesis of acetylated amino acids. ACY1 may also play a role in xenobiotic bioactivation as well as the inter-organ processing of amino acid-conjugated xenobiotic derivatives (S-substituted-N-acetyl-L-cysteine). This family includes Staphylococcus aureus amidohydrolase, SACOL0085, which contains two manganese ions in the active site, and forms a homotetramer with variations in interdomain orientation which possibly plays a role in the regulation of catalytic activity.	0
NZ_CP017704.1|WP_063232259.1|1393694_1394021_-|DUF1878-family-protein	gnl|CDD|370213	pfam08963, DUF1878, Protein of unknown function (DUF1878). This domain is found in a set of hypothetical bacterial proteins.	2.96166e-23
NZ_CP017704.1|WP_063232248.1|1381120_1382056_-|ferrochelatase	gnl|CDD|183526	PRK12435, PRK12435, ferrochelatase; Provisional.	0
NZ_CP017704.1|WP_065310849.1|1379969_1380098_+|YhfH-family-protein	gnl|CDD|379490	pfam14149, YhfH, YhfH-like protein. The YhfH-like protein family includes the B. subtilis YhfH protein, which is functionally uncharacterized. Its expression is repressed by the Spx paralogue MgsR, which regulates genes involved in stress response. This family of proteins is found in bacteria. Proteins in this family are typically between 42 and 53 amino acids in length.	4.05546e-14
NZ_CP017704.1|WP_063232258.1|1392562_1392925_+|YtxH-domain-containing-protein	gnl|CDD|227313	COG4980, GvpP, Gas vesicle protein [General function prediction only].	2.59262e-15
NZ_CP017704.1|WP_063232254.1|1389521_1389944_+|HIT-family-protein	gnl|CDD|238608	cd01277, HINT_subgroup, HINT (histidine triad nucleotide-binding protein) subgroup: Members of this CD belong to the superfamily of histidine triad hydrolases that act on alpha-phosphate of ribonucleotides. This subgroup includes members from all three forms of cellular life. Although the biochemical function has not been characterised for many of the members of this subgroup, the proteins from Yeast have been shown to be involved in secretion, peroxisome formation and gene expression.	1.80466e-56
NZ_CP017704.1|WP_063232249.1|1382134_1383178_-|uroporphyrinogen-decarboxylase	gnl|CDD|234644	PRK00115, hemE, uroporphyrinogen decarboxylase; Validated.	0
NZ_CP017704.1|WP_063232253.1|1386916_1388125_-|ABC-transporter-permease	gnl|CDD|377581	pfam05975, EcsB, Bacterial ABC transporter protein EcsB. This family consists of several bacterial ABC transporter proteins which are homologous to the EcsB protein of Bacillus subtilis. EcsB is thought to encode a hydrophobic protein with six membrane-spanning helices in a pattern found in other hydrophobic components of ABC transporters.	1.33546e-116
NZ_CP017704.1|WP_063232256.1|1391447_1391966_+|tryptophan-transporter	gnl|CDD|293704	pfam17099, TrpP, Tryptophan transporter TrpP. TrpP is a bacterial transmembrane protein that is probably involved in tryptophan uptake. Its expression is regulated by tryptophan-activated RNA-binding regulatory protein (TRAP).	3.34418e-38
NZ_CP017704.1|WP_063232247.1|1380261_1380837_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.78658e-14
NZ_CP017704.1|WP_063232255.1|1390217_1391321_+|3-phosphoserine/phosphohydroxythreonine-transaminase	gnl|CDD|235428	PRK05355, PRK05355, 3-phosphoserine/phosphohydroxythreonine transaminase.	0
NZ_CP017704.1|WP_063232251.1|1384149_1384773_-|phosphatase-PAP2-family-protein	gnl|CDD|239486	cd03392, PAP2_like_2, PAP2_like_2 proteins. PAP2 is a super-family of phosphatases and haloperoxidases. This subgroup, which is specific to bacteria, lacks functional characterization and may act as a membrane-associated lipid phosphatase.	2.0992e-35
NZ_CP017704.1|WP_063232260.1|1394263_1394803_+|DUF3267-domain-containing-protein	gnl|CDD|378690	pfam11667, DUF3267, Putative zincin peptidase. This family of proteins has a conserved HEXXH motif, suggesting the members are putative peptidases of zincin fold.	4.57947e-14
NZ_CP017704.1|WP_063232413.1|1386106_1386811_-|EcsC-family-protein	gnl|CDD|378945	pfam12787, EcsC, EcsC protein family. Proteins in this family are related to EcsC from B. subtilis. This protein is found in an operon with EcsA and EcsB which are components of an ABC transport system. The function of this protein is unknown.	2.11462e-85
NZ_CP017704.1|WP_063232250.1|1383449_1383965_+|antibiotic-biosynthesis-monooxygenase	gnl|CDD|225209	COG2329, COG2329, Uncharacterized enzyme involved in biosynthesis of extracellular polysaccharides [General function prediction only].	4.91053e-19
NZ_CP017704.1|WP_048677969.1|1388117_1388861_-|ABC-transporter-ATP-binding-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	1.36206e-81

Protein sequences

>NZ_CP017704.1|WP_048677969.1|1388117_1388861_-|ABC-transporter-ATP-binding-protein
MSLLEIKQLVGGYTKTPVLKGISFDIQPNELVGLIGLNGAGKSTTIKHIIGLMEPKGGSVSIHGKTLAQDPDTYRKQFTYVPETPILYDELTLEEHLKLTAMAHGLAEATFKERMDVLLKEFHMEKRLKWFPAHFSKGMKQKVMIMCAFLVQPSLYIVDEPFVGLDPLGIQSLLDLMRKMKESGAGILMSTHILATAERYCDSFIILHNGEIRAKGNLEQLREQFSMPGATLDDLYIQLTKEEIGHE
>NZ_CP017704.1|WP_063232253.1|1386916_1388125_-|ABC-transporter-permease
MNSQNLWKERYLGYINETQKYLRYIFNGHLVFVMVLVLGGLAYYYSDWVKTLDSDFPAELIMAFVLSIIVTRSPINTFLKEPDTVFLLPLETKLRSYFKNSLILSWVMQGFILLVVLIASMPMYSKVTGAGGTDLGIILVVLLILKFLNLTMRWQVLKYQDTSVSHWDSLIRFLLNGVILYFICSRANILFSLITFLILLALYMYYRSATKGFVLKWERLVELENKRMNSFYRIANMFTDVPHLKGKVARRKWMDWLLSFIPYGEKSTYTYLYARTLLRSNDYVGLCFRLTIIGSVILSVFTNIWAHLIVTFMFLFMTALQLLPVWKAHEWKVWVSLYPLPAKMRESAVIKLISYFLLFEDLVFSLVLLVKGEWMSALAALAMGLVFLFGFKIYAAKKIKNF
>NZ_CP017704.1|WP_063232413.1|1386106_1386811_-|EcsC-family-protein
MDEYGQKALSELVSWKKKVAKKSGRLERMSKKAQIKLNSYIPDRVHKMITDSIKGMIEAVLSGSKYMSKEKNVVLLSLQQKEEWVAETVTAYRKTAVIEGVGTGAAGLLIGLADFPLLLSIKMKLLFEISRIYGFDPNKYEERLFILHIFQMAFSSEEKKLETLRVIEEWDSGKWPEIDWQEFQQEYRDHIDVIKMFQLVPGFGAAVGAYANHHLLEHLGETAVNCYRIRLLKE
>NZ_CP017704.1|WP_063232252.1|1384865_1386077_+|amidohydrolase
MIQRLHNLLDGSYEEMVSIRRYLHQHPELSFQETQTAAFIAGYYEKLGIEHRTNVGGNGVIAKVTGNKPGKTVALRADFDALPIQDEKEVSYKSSVPGVMHACGHDGHTATLLVLAKNLNELKDELEGEYIFIHQHAEEYAPGGAKPMIEAGCLDGVDVIFGTHLWATVPTGTVQYAYGPIMAAADRFEIIIQGQGGHGAQPHKTRDAIVVGSQLVMALQQIVSRRLNPIDSAVITVGSFVADNAFNVIADKAKIIGTVRTFKEDVRSFISEEMERIVKGTCLAADCTYEYQYFQGYPAVIPHVEETKFLIESTESVKEVLITEEIDPDMTGEDFSYYLQNVKGTFFFTGARPKNEHTYPHHHPLFDIDEKAMLIAAKILGTAAVTYHNKKQSSQKVNESLLR
>NZ_CP017704.1|WP_063232251.1|1384149_1384773_-|phosphatase-PAP2-family-protein
MIKYSWIAMVLLCLLLFFFLMHEVQSEKTLAFDTYIAELFSVGENTFSFTFFKSITYLGKSKFIGFGSLLCVLYLWIIKKDYWTMAVFSIGVTGGDVLNGWIKNHIQRARPENHLMETTGFSFPSGHAMVGLIFFSMVAYLIIKEVKGDFLKWAVGIGFVCMVLLIGVSRIIMKVHFPTDILAGFALGAAYSLTLFNLYKYLGRRVL
>NZ_CP017704.1|WP_063232250.1|1383449_1383965_+|antibiotic-biosynthesis-monooxygenase
MNVFITSGSFDFLKIKKDKHPNEKILLMQNPGTAVLLHETAGKTIFSSPRKYEVVDGKGNLQDHGYVVMNNIPVSEEGRPVFEHRFKNRAEFIENEPGFVALRVLRPINSETYVILTIWEKQTDFLNWKKSSSFQKAHNSDSKAPVTNSSQKMFSGEAYVTQYTLVKDSEE
>NZ_CP017704.1|WP_063232249.1|1382134_1383178_-|uroporphyrinogen-decarboxylase
MSKEITNDTFLKAARGEKTDHVPVWYMRQAGRSQPEYRKLKEKYSLFEITHQPELCAYVTRLPVEQYDVDAAILYKDIMTPLPAIGVDVEIKSGIGPVISNPIKSVTDVEKLGELNPEKDIPYVLDTIKLLTTEQLSVPLIGFSGAPFTIASYMIEGGPSKNYNKTKAFMYSEPKAWFALMDKLADMIIIYVKSQIKAGVKAVQIFDSWVGALNVEDYRVFIKPIMTRIFSSLREENVPLIMFGVGASHLALEWNDLPIDVVGLDWRLPITEARQMGIQKTVQGNLDPALLLSSWDVIEERTKRILDQGMEQDGYIFNLGHGVFPSVNPETLKRLTAFIHEYSSKMK
>NZ_CP017704.1|WP_063232248.1|1381120_1382056_-|ferrochelatase
MSRKKMGLLVMAYGTPYTEEDIERYYTHIRHGRRPSDELIADLKGRYEAIGGLSPLAKITAGQAEALEKKLNSVQEEVEFKAYLGLKHIEPFVEDAVKQMHEDGIKEAVSIVLAPHFSTFSVKSYNGRAEDEAAKLGDLTITSVESWYDEPKFIQYWVDQVKEVIGKMTSEERDNFALIVSAHSLPEKILQSGDPYPNQLKETADMIAKGAGVTNYAVGWQSAGQTPEPWLGPDVQDLTRDLHQAKGYKAFIYIPVGFVAEHLEVLYDNDYECKVVTEDIGACYYRPDMPNVKPEFIDALATIILNKLQEK
>NZ_CP017704.1|WP_063232247.1|1380261_1380837_-|TetR/AcrR-family-transcriptional-regulator
MSVDRKKLILEAATKSFSLFGYKATTMDQVAKIANVGKGTIYTFYKNKEELFKEIVQRMIEEMKYEAEQSLDDQLSFFENLHRAVYRILEFRQEHQLSLKLLQEEREIGTPAVQEMVNEMEEAIVSYIKEKLKIAIEKGYIQPCDPEITAFLMLKMYLALIFDWERNHAPLEKEEIAELFKIYLFKGLSVT
>NZ_CP017704.1|WP_065310849.1|1379969_1380098_+|YhfH-family-protein
MIQSSVEFFKNLPPKQCTECGKKIEEQHECYGNHCDHCLSGE
>NZ_CP017704.1|WP_063232254.1|1389521_1389944_+|HIT-family-protein
MSDCIFCKIIDGEIPSTKVFENEHVLAFLDISQVTKGHTLVIPKVHKENLYELTPEIAKNLFEVVPEIARAMKQEFQPVGLNLLNNNGEAAGQSVFHFHMHLIPRHGEGDGFGAVWKTNTSDYTPDDLKQIADSIAQHLK
>NZ_CP017704.1|WP_063232255.1|1390217_1391321_+|3-phosphoserine/phosphohydroxythreonine-transaminase
MKRAHNFNAGPAALPLEVLQRAQNEWLNIEDSGMSVMELSHRSSEFEKIHNHAIQSLKDLMEIPENYEVLLLQGGASLQFSMIPMNILNDGKRADYVLTGSWSEKALKEAKKVGETAVVASSKDEKYTFIPKVEDIKLNDDAAYLHITSNNTIYGTQWKEFPETGDIPLVADMSSDILSKKIDISKFGIIYAGAQKNLGPSGITVVIIRKDLITDNDKIPSMMNYSIHSKNKSLYNTPPTLAIYLLSLVLDWAKEQGGVEKIAEINEEKAKVIYDAIDGSDGFYKGHALPDSRSLMNVTFTLPSEEAEVQFLNEVKQAGFVGLNGHRSIGGCRASIYNAVPLSHCQDLADFMKNFQESYKAKEAQTL
>NZ_CP017704.1|WP_063232256.1|1391447_1391966_+|tryptophan-transporter
MKTKTLVSLSLLIGIGAALHFIVPGFFLGMKPDMMLLMMFLAITLFPAKKNVFIVALAAGAISAMTTTFPGGQIPNIIDKLATAFLFYLLFISLKKFSTSVVTVSILTALGTMISGAVFLGSAYYIVSLPGPFVALFGAVVLPAVLLNTVAMVIIYPIVNGIVRKSNIPINA
>NZ_CP017704.1|WP_063232258.1|1392562_1392925_+|YtxH-domain-containing-protein
MKAKSLLIGFLTGTVVAGAATLLSTPSSGKDLRTRIKSNTDEIKNTIDELKVKMLNIKDDTMEASQISKETVKTFISDVQVVIENWKREIEPNKNELLKNVQEIENSLKELEAATPSSKN
>NZ_CP017704.1|WP_034314691.1|1393113_1393692_+|HTH-type-transcriptional-regulator-Hpr
MQNKNYSMKEAMIFSQRIAQLSKALWKSIEKDWQQWIKPYDLNINEHHILWIAYHLNGSSISDVAKFGVMHVSTAFNFSKKLEERGYLTFSKKENDKRNTYIEITAEGEKILLDLMETYDPSKNSAFSGALPLRELYGKFPDMIEMMAIIRNIYGEDFMQIFERSFDNIDQEFTDVEGKITKKKIEKETEPV
>NZ_CP017704.1|WP_063232259.1|1393694_1394021_-|DUF1878-family-protein
MKNINEEIEILRFHQRLLLNLIRNPEAKLDYLFVEKNFTKQEAEELLETCDILSKRYEIEKAEGYMNFRPLFNQFERKVNPKITIKECIDACLSQGLYVSFMKEMDRV
>NZ_CP017704.1|WP_063232260.1|1394263_1394803_+|DUF3267-domain-containing-protein
MNSWKTIDVAKQYGNCRLIFFSVFTILMSFVLIYTLFSVFSTHVILYGDQTMVFFSLLFLLYPVHKLLHYLPLRLLCKKVKTSWSLKWNLVLTCKVNVHYPIRKHLYLFTLVLPFFIMTVILIGCALSFPHYIHYFTILLSLHTGLCVSDFIYIKNLVGSPRNSFIEEHLEGYDILIQK
>NZ_CP017704.1|WP_034314696.1|1394911_1395094_+|hypothetical-protein
MISFWFIIFAILILYNINRMTNSLCIQKEIAEDRQPKVFRTINVLITIMLLSSYIEILYT
>NZ_CP017704.1|WP_061462016.1|1395206_1395290_-|YjcZ-family-sporulation-protein
MSGGIGGGFALIVVLFILLIIIGASWL
>NZ_CP017704.1|WP_081112840.1|1395473_1395557_-|YjcZ-family-sporulation-protein
MSNGFNGGFALLVVLFILLIIVGSACC

Crispr_ID: NZ_CP017704_3

• CRISPR_ID: NZ_CP017704_3
• CRISPR_location: 4909179-4909265
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP017704_3

Consensus_repeat	Method
GCTGAATATCGGAGCTGTCTTTAAGGCA	CRISPRCasFinder

spacers of NZ_CP017704_3

>3.1|4909207|31|NZ_CP017704|CRISPRCasFinder
GCTTTTTCTTATGGAACTAACGGGTGCGTTA

CRISPR arrays and Neighbor proteins around NZ_CP017704_3

CRISPR arrays

The CRISPR arrays of NZ_CP017704_3

>merge|NZ_CP017704|3|4909179-4909265|CRISPRCasFinder
GCTGAATATCGGAGCTGTCTTTAAGGCAGCTTTTTCTTATGGAACTAACGGGTGCGTTAGCTGAAGATCGGAGCTGTCTTTAAGGCA

>NZ_CP017704|3|3|4909179-4909265|CRISPRCasFinder
GCTGAATATCGGAGCTGTCTTTAAGGCA	GCTTTTTCTTATGGAACTAACGGGTGCGTTA
GCTGAAGATCGGAGCTGTCTTTAAGGCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP017704.1|WP_063234340.1|4918207_4918639_-|hypothetical-protein	unknown	unknown	gnl|CDD|274476
NZ_CP017704.1|WP_063236557.1|4907999_4908203_-|alpha/beta-type-small-acid-soluble-spore-protein	unknown	unknown	gnl|CDD|365990
NZ_CP017704.1|WP_144479075.1|4915199_4915385_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP017704.1|WP_094246656.1|4897845_4898070_+|transcriptional-regulator	unknown	unknown	gnl|CDD|379188
NZ_CP017704.1|WP_063234337.1|4912495_4913740_+|serine-hydrolase	unknown	unknown	gnl|CDD|365903
NZ_CP017704.1|WP_063234341.1|4919065_4921240_+|DNA-topoisomerase-III	unknown	unknown	gnl|CDD|236078
NZ_CP017704.1|WP_063236554.1|4910202_4910547_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP017704.1|WP_056527673.1|4901333_4901951_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|379534
NZ_CP017704.1|WP_063236535.1|4902245_4903940_+|CocE/NonD-family-hydrolase	unknown	unknown	gnl|CDD|225487
NZ_CP017704.1|WP_063236300.1|4898136_4898325_+|twin-arginine-translocase-TatA/TatE-family-subunit	unknown	unknown	gnl|CDD|237837
NZ_CP017704.1|WP_063234342.1|4921342_4921771_+|transcriptional-regulator-MntR	unknown	unknown	gnl|CDD|179669
NZ_CP017704.1|WP_081113119.1|4910787_4910889_+|LPXTG-cell-wall-anchor-domain-containing-protein	unknown	unknown	unknown
NZ_CP017704.1|WP_063236558.1|4907187_4907688_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP017704.1|WP_094246658.1|4899421_4900696_+|IS110-family-transposase	unknown	unknown	gnl|CDD|376564
NZ_CP017704.1|WP_063234339.1|4915495_4917034_-|multicopper-oxidase-domain-containing-protein	unknown	unknown	gnl|CDD|259958
NZ_CP017704.1|WP_063236555.1|4909434_4909953_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP017704.1|WP_094246657.1|4898388_4899126_+|twin-arginine-translocase-subunit-TatC	unknown	unknown	gnl|CDD|223876
NZ_CP017704.1|WP_063236556.1|4908478_4909135_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP017704.1|WP_094246659.1|4911011_4911461_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP017704.1|WP_063236534.1|4904259_4905198_+|magnesium-transporter-CorA-family-protein	unknown	unknown	gnl|CDD|213361

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP017704.1|WP_063234340.1|4918207_4918639_-|hypothetical-protein	gnl|CDD|274476	TIGR03187, hypothetical_protein, DGQHR domain. This highly divergent, uncharacterized domain has several absolutely conserved residues, including a QR pair and FxxxN motif. Its most striking feature, however, is a near invariant pentapeptide motif DGQHR. Several different subfamilies occur specifically as a part of DNA phosphorothioation systems, previously called DND (DNA instability during electrophoresis), while others (e.g. CPS_2936) occur in other contexts suggestive of lateral gene transfer (sporadic distribution of helicase-containing cassettes). The region described by this model is about 280 amino acids in length; additional sequences show local sequence similarity.	8.03148e-06
NZ_CP017704.1|WP_063236557.1|4907999_4908203_-|alpha/beta-type-small-acid-soluble-spore-protein	gnl|CDD|365990	pfam00269, SASP, Small, acid-soluble spore proteins, alpha/beta type.	1.84401e-21
NZ_CP017704.1|WP_094246656.1|4897845_4898070_+|transcriptional-regulator	gnl|CDD|379188	pfam13443, HTH_26, Cro/C1-type HTH DNA-binding domain. This is a helix-turn-helix domain that probably binds to DNA.	0.000608899
NZ_CP017704.1|WP_063234337.1|4912495_4913740_+|serine-hydrolase	gnl|CDD|365903	pfam00144, Beta-lactamase, Beta-lactamase. This family appears to be distantly related to pfam00905 and PF00768 D-alanyl-D-alanine carboxypeptidase.	1.86897e-59
NZ_CP017704.1|WP_094246658.1|4899421_4900696_+|IS110-family-transposase	gnl|CDD|376564	pfam01548, DEDD_Tnp_IS110, Transposase. Transposase proteins are necessary for efficient DNA transposition. This family includes an amino-terminal region of the pilin gene inverting protein (PIVML) and of members of the IS111A/IS1328/IS1533 family of transposases. The C-terminus is represented by family pfam02371.	1.50822e-27
NZ_CP017704.1|WP_063236535.1|4902245_4903940_+|CocE/NonD-family-hydrolase	gnl|CDD|225487	COG2936, COG2936, Predicted acyl esterases [General function prediction only].	2.5955e-124
NZ_CP017704.1|WP_063236300.1|4898136_4898325_+|twin-arginine-translocase-TatA/TatE-family-subunit	gnl|CDD|237837	PRK14861, tatA, twin arginine translocase protein A; Provisional.	4.38127e-25
NZ_CP017704.1|WP_063234342.1|4921342_4921771_+|transcriptional-regulator-MntR	gnl|CDD|179669	PRK03902, PRK03902, transcriptional regulator MntR.	5.86484e-92
NZ_CP017704.1|WP_063236534.1|4904259_4905198_+|magnesium-transporter-CorA-family-protein	gnl|CDD|213361	cd12827, EcCorA_ZntB-like_u2, uncharacterized bacterial subfamily of the Escherichia coli CorA-Salmonella typhimurium ZntB family. A uncharacterized subfamily of the Escherichia coli CorA-Salmonella typhimurium ZntB (EcCorA-ZntB_like) family of the MIT superfamily of essential membrane proteins involved in transporting divalent cations (uptake or efflux) across membranes.The EcCorA-ZntB-like family includes the Mg2+ transporters Escherichia coli and Salmonella typhimurium CorAs, which can also transport Co2+, and Ni2+. Structures of the intracellular domain of EcCorA-ZntB-like family members, Vibrio parahaemolyticus and Salmonella typhimurium ZntB, form funnel-shaped homopentamers, the tip of the funnel is formed from two C-terminal transmembrane (TM) helices from each monomer, and the large opening of the funnel from the N-terminal cytoplasmic domains. The GMN signature motif of the MIT superfamily occurs just after TM1, mutation within this motif is known to abolish Mg2+ transport through Salmonella typhimurium CorA. Natural variants such as GVN and GIN, such as occur in some ZntB family proteins, may be associated with the transport of different divalent cations, such as zinc and cadmium. The functional diversity of MIT transporters may also be due to minor structural differences regulating gating, substrate selection, and transport.	8.81273e-109
NZ_CP017704.1|WP_056527673.1|4901333_4901951_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|379534	pfam14278, TetR_C_8, Transcriptional regulator C-terminal region. This domain is a tetracycline repressor, domain 2, or C-terminus.	3.89091e-20
NZ_CP017704.1|WP_063236555.1|4909434_4909953_+|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.	3.68565e-17
NZ_CP017704.1|WP_094246657.1|4898388_4899126_+|twin-arginine-translocase-subunit-TatC	gnl|CDD|223876	COG0805, TatC, Sec-independent protein secretion pathway component TatC [Intracellular trafficking and secretion].	1.09894e-63
NZ_CP017704.1|WP_063234341.1|4919065_4921240_+|DNA-topoisomerase-III	gnl|CDD|236078	PRK07726, PRK07726, DNA topoisomerase 3.	0
NZ_CP017704.1|WP_063234339.1|4915495_4917034_-|multicopper-oxidase-domain-containing-protein	gnl|CDD|259958	cd13891, CuRO_3_CotA_like, The third Cupredoxin domain of bacterial laccases including CotA, a bacterial endospore coat component. CotA protein is an abundant component of the outer coat layer in bacterial endospore coat and is required for spore resistance against hydrogen peroxide and UV light. CotA belongs to the laccase-like multicopper oxidase (MCO) family, which are able to couple oxidation of substrates with reduction of dioxygen to water. MCOs are capable of oxidizing a vast range of substrates, varying from aromatic compounds to inorganic compounds such as metals. Although the members of this family have diverse functions, majority of them have three cupredoxin domain repeats. The copper ions are bound in several sites: Type 1, Type 2, and/or Type 3. The ensemble of types 2 and 3 copper is called a trinuclear cluster. MCOs oxidize their substrate by accepting electrons at a mononuclear copper center and transferring them to the active site trinuclear copper center. The cupredoxin domain 3 of 3-domain MCOs contains the Type 1 (T1) copper binding site and part the trinuclear copper binding site, which is located at the interface of domains 1 and 3.	2.2902e-78

Protein sequences

>NZ_CP017704.1|WP_063236556.1|4908478_4909135_+|hypothetical-protein
MKVEISYFPPEKIITVPEEEATYPFEINGEFQYIVEFYTDTHEEFFCNWMDSPDYYPIYSLAEIYDFQQAEYEELFKMQNIEFNYMKGSRKDTFFVKAIIRSPQQFKEYYSYLYGNGSMLNLPLWSLKQDVFRLEEREYESPYPVKKTKNNRTRLVKLKWIANTPIATLVASSTMFWVGYDGDYITAFSNDEHFSTIDSLQKIIPEKVELVTGDYEYE
>NZ_CP017704.1|WP_063236557.1|4907999_4908203_-|alpha/beta-type-small-acid-soluble-spore-protein
MARNNNNNQLVVNGAEQALEQMKYEISSEFGVTLGADTTSRANGSVGGEITKRLVQMAEQQLGGRTR
>NZ_CP017704.1|WP_063236558.1|4907187_4907688_+|hypothetical-protein
MKIRWFIYLVIGIVFGVFDFYFHSFISNVLVQGETFWTVLTYGVWLVPIVPIALYEVRISKSRVRAALASSSTWLVSIIFYYLYNAIQLGIIGRSTRPELHISNHKDPFFWGNWKNVFWEDIVIRGIVEWSVVVVAGGFIVGFSVGFIYLLLEKLIKLRRTTNEDF
>NZ_CP017704.1|WP_063236534.1|4904259_4905198_+|magnesium-transporter-CorA-family-protein
MFITYKSSREGILEIIEKFEKDCWINMTAPSKEELTEVSQLCNIPIEFLRDPLDLEESARIQYDQETNCTLIINDFPTIDMNHGQFDSYITIPIGIILGTDYIVTVCNQSTNSLENVIKKNVNTSMKSRFALEILFSISTQYIEKLKQLNKQRLKIENNLRDSLTNKQLYDLMEIEKSLVYFLTSLKGNGDIITKLFRANSVKLYEDDKDLLEDVKIENNQGIETTELYTRILNSITGSYSSLISNELNNTMKTLTLFTVFLTLPTLVFSFFGMNVTLPIGDQDPFSWMIILIIALIFIALIGLALWRRRIS
>NZ_CP017704.1|WP_063236535.1|4902245_4903940_+|CocE/NonD-family-hydrolase
MNKFLGRPDQKTTHPNDTKPGLNKIVMTTAHYGNQEMIMEKDVPIKMQDGVTIYVNVFRPNKPGKFPVVMSMDPYNKDGFPPYDTFRQVWPTVGTIVTSLFAPFESPDPGFWVPNDYILIKIATRGSSNSEGDLYPWTKTETQDYYEVIEWAGVQEWSDGNVGLNGVSYLAMTQWRVAAMNPPHLKAIIPWEGTSDLYREWYFHGGIPETVFSADFEKLQHTRWPNNNIEEMVAAQKEHPLLDEHWEERQVTLSDIKVPMFVCASWSTQGLHNRGTFEGFKQASSKDKWLLVHGRKEWETYYLRESLEQQKEFFDYFLKGIENDWMDTPRVRYEVREKFYKGHIRTANEWPIAQTKYSKQYLNGEEMSLQQTPVQNETRLTYNAEPGQTENSDLRFKFPADEDIELTGNMKLKLWVSAEDTDDMDIFVGIKKYDRRGNEVFLPDFNHIENGQVANGWLRVSHRELDPERSTPYQPVLKHKRLLKLNKGEIVPVEIEILPSSILLRDGESLVLVIKGSEIIIEENPSGDTRRYGHKETVNKGTHSIYTGGKYDSFLLVPVIPKKE
>NZ_CP017704.1|WP_056527673.1|4901333_4901951_-|TetR/AcrR-family-transcriptional-regulator
MRNSNTDLRVIRTKESIRHALVELINEKGFEAITVKDITIRAKINRGTFYAHYQDKFDLMTKCEEEIMLDMSRITKQNFPSVIAALETDSQTLTPFSLTVSLFEYLNINSGFMKAVLGPKGDLSFQTRLKEFMWETLYGNNPNAFIKEENFLVPGQYLASYMGTAIIGVIQQWLESGRKESPQEMARILTTITANGPYFAAGLKK
>NZ_CP017704.1|WP_094246658.1|4899421_4900696_+|IS110-family-transposase
MKFKMQDKQNQLIERISDKHLVVGVDIAQQLHVARAVNFRGIVVGDPLAFENNEDGFASLLKWMDKLQRLNKLDAAIVGMEPTGHYWINLSKWLFKQGIEVVKVNPHLVKRNKENRDNTQSKSDKKDALVIADMVKNGYYAFVRNTSESFEILRVLMSNRDVVVKRLVSTINQLNRWVDIVFPELRQVFKDITGKGAIATLRLFPSPMELRSLKPHDVVSGWKSIMKRQPGLKKAQLLLQLARKSVGTRQALEAYKFHLEQLLEEYDLAVLQLERVEQEVKDVLKQIPFAKKLLAIKGISEISLAGILGEAGDLSGFSHGNSLLRHAGLHLAEASSGKWKGQIVISKRGRSRLRRFLYLATMSLVMNNTEFRAIHTHNVKVKKMKKMKSIMKLVGKLARIFVGIARRNESYCADKVQPITELVA
>NZ_CP017704.1|WP_094246657.1|4898388_4899126_+|twin-arginine-translocase-subunit-TatC
MEGQNMNVVQHIEELRKRIIITLVAFLLFLALAFIYVQDIYHVIVEDLPFKLAVLGPSDILFVYLMIASVVAITVTIPVAAHQVWLFVRPALTQNERKVTIAYIPALFILFVLGISFGYYILFPLVLKFLMSLSNDMFTTFFTTEKYFRFLLHMTLPFGFLFEMPVVIMFLTSLGIINPYRLQKMRKYAYFILIVVSILITPPDFLSDILVIIPLLLLYESSISLSKFVYKRQQRAKEGKKDVYE
>NZ_CP017704.1|WP_063236300.1|4898136_4898325_+|twin-arginine-translocase-TatA/TatE-family-subunit
MLQNIGIPGLILVLIIALIIFGPSKLPEIGRAFGSTLREFKKSTRELVTDDTNIETSNKKNN
>NZ_CP017704.1|WP_094246656.1|4897845_4898070_+|transcriptional-regulator
MMKLGKKRSNFGRWVDKQKDINKLELERASNLSRMTISKLCSDPDYRPRFSTVIKINQGLKKLGKNMDLNDFFY
>NZ_CP017704.1|WP_063236555.1|4909434_4909953_+|GNAT-family-N-acetyltransferase
MEIRKARKEDIKGISRVYVDSWRTTYRDLVPDDYLDELSYEDAEKRWNDFLYNENEPFIYVAINETGKIIGFASGKSIDEKNYDGELYSLYLLQECRGFGVGRQLISAIAKHFKEKGFYSMMVWVMKQNNSGLGFYERMGGKEYIHRTSTFGGTIVEDIAYGWKDISELCIE
>NZ_CP017704.1|WP_063236554.1|4910202_4910547_-|hypothetical-protein
MIFLALLLMLGGLLIINAIYAYHTKHIDSNFLSTLWYYIKLLPLFLPASIMIGYGVKFLTKIVDNLTFSLIVSKGMEILVSVAIGYIFLKEIPNWRTGVGITIILIGFWLLKGK
>NZ_CP017704.1|WP_081113119.1|4910787_4910889_+|LPXTG-cell-wall-anchor-domain-containing-protein
MLGDIIYQVIVFGGISLILGVLGYLFFKRTKKS
>NZ_CP017704.1|WP_094246659.1|4911011_4911461_+|hypothetical-protein
MLFHIIIGFILPWIVGVYLFRNQKKLFIIFYPIGTATSFLINEIGFNYFWRMDIVFQESSLTGIPYDLGLYPILGCLFICVIHYKKMPILITFLVFTLVTTFGEYILVCLEKIVYRNEWNIIWTGVSYLFAYSIFYVYYKLVRKFILLN
>NZ_CP017704.1|WP_063234337.1|4912495_4913740_+|serine-hydrolase
MKKITTGQSNTGLSETGLRRMRDVLARHVESGKIPGLVALVSRYGETHVEAIGTMRHDGGAPMRRDTIFRLASTSKPLAVASVMILLDECKLHLDDPVDTWLPELADRQVLKRADGPLDDTVPARRPITIRDLLTSTFGLGVDITLMGSPIQNAIFESGIYDTPGAELPDPDEWMRRLGTLPLSYQPGERWQYHVSNEVLGVLVARVTGQTFETFLRERILDPLGMKDTGFYVPANKIDRLPPAFNPDPQTGEFIVWDEAAGGRYSRPPAFQAGGGGLLSTVDDYHAYLRMLLNQGMHGTERILSRPAVQLMTTNRLTPEQQAARDALAKNNVHLSHGQGQHGGWGFGMAVRTYRGDYASIGQFGWDGGTGTTTYADPDKQLTGILLTQVGMSTPDSARLIHDFWTMVYQAIED
>NZ_CP017704.1|WP_144479075.1|4915199_4915385_+|hypothetical-protein
MTFKSEIIKICIAIVITFLLGRTVSQGIQIELLRDIVVGITVAVVYLLLIIRFLKRSDDDE
>NZ_CP017704.1|WP_063234339.1|4915495_4917034_-|multicopper-oxidase-domain-containing-protein
MILSKFVDELPIPPILKPRWKDQFYTYYEVNMTEFKQSLHRELNDTTVWGYEGSYPGPTIEVERGEIVFIKWINNLPDKHLFPVDYTVHGAHMDVPEVRTVVHVHGACVESESDGYPEAWFTKEFKQVGRYFRKQVYRYDNCGHDSTLWYHDHALGITRLNVYAGLAGFYLIRDQHERLLNLPSEQYEIPLMIQDKTFNKDGSLYYPKQPDQPIPKLETSIIPEFVGDTIIVNGKVHPYLKVEPRKYRFRLLNASNTRFFRMKLDSEQPMYQIATDGGLMQHPIGVKEIMLAPAERAEVIIDFTNLEGKYIIMTNDAPAPFPTGNGNQINENTGTVMQFRVILPLSSVDTSVIPAYMMPVPKIREQLASKVRYLTLNDNMDKYGREFMLLDNKQWDAPITENPKLGSTEIWCLINLTTDTHPIHLHLIDFQILDRRDFDVQRYKKEKIIHYTGPAISPEPYERGWKDTVQSNPNQVTRIIMKFGPYTGLYVWHCHILEHEDYEMMRPYIVIR
>NZ_CP017704.1|WP_063234340.1|4918207_4918639_-|hypothetical-protein
MYNKGTLIGKRTKEKHITLQNVYNFLLLLIKNTKLAELPKEKILNITLTYFNCIKELLPVEWSDYKQYRLTHIVCLNAFAIAGNKIIPSNYNFVSNQLNIKEVNKRMSSIKIFDWSSEGTLKYLKGASGSKLLAEDIIASVEK
>NZ_CP017704.1|WP_063234341.1|4919065_4921240_+|DNA-topoisomerase-III
MKLIIAEKPDQGSTLAAQFKTKKQQGYIEIMPNELFPDGAYVTWAVGHLCQLVSPETYHSKWKKWSMETLPMIPEKFQYEVTRQKAKQFNVVKTLLRKPDVDEIIHAGDAGREGELIVRNIVNLCNVNKPMKRLWISSLTPKAIYEGFQNLKNEEKTRPLYYEAYTRACADWVVGMNASRAYSILLQQRGVSDVFSAGRVQTPTLALIVKRELEIEQFKSEPFWEVFADFKMDGKKYQGKWQQNNDPRIKTKEMAEKIAAFCKGKEAEIAEMDTERKEFQPPLLFNLSSLQATVNKIYKYSPKQTLDIVQSLYQKGIVSYPRSDSNYVTEGEAETFPDILQKLSGFSEYESLFPLPQPNIMNNKRFVNEKKVTDHYAIIPTEQVTDPKRLSAEERNIYDLVVRRLIAAHYEKAIFDYTTIKTLVDKRAEFISKGKQQIQEGWRKVIFQNDKDDDDIILPSVSKGDSGKVSNIKVKEGKTQPPKRYTEGQLITLMKTAGKHLDNEELEKVLMKTEGLGTEATRAGIITMLKDRKYINVKKNQVFATDKGKVLITAIGEKILASPEMTAKWEQRLREIGEGKASAGGFMEAVKKMSAKIISDAVESSESWDFQGLDTESIQRSGPKKRSSASMGSCKLCGSKIVDKGEFYGCVSYQKTKCNFTISKKILNKKISQANIKKLLASGETDMISGFIKGEKTFDAILSWSDSEKKISFTFPTEQNVKQT
>NZ_CP017704.1|WP_063234342.1|4921342_4921771_+|transcriptional-regulator-MntR
MPTPSMEDYIEQIYLLIEEKGYARVSDIAENLSVHPSSVTKMVQKLDQEKYLIYEKYRGLVLTANGKKVGKRLVYRHELLEQMLRLIGVKEENIYHDVEGIEHHLSWNAIDRIGDLVEFFEESPDRVEDLRKIQKRNEENSK

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NC_013793	Bacillus pseudofirmus OF4 plasmid pBpOF4-02, complete sequence	19473-19503	4	0.871
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP043831	Bacillus sp. BS98 plasmid unnamed1	242677-242707	6	0.806
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP017081	Bacillus muralis strain G25-68 plasmid pG25-68, complete sequence	84131-84161	6	0.806
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP017081	Bacillus muralis strain G25-68 plasmid pG25-68, complete sequence	34956-34986	6	0.806
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP017081	Bacillus muralis strain G25-68 plasmid pG25-68, complete sequence	72849-72879	6	0.806
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP033045	Bacillus foraminis strain Bac44 plasmid unnamed, complete sequence	136268-136298	6	0.806
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP011009	Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence	18430-18460	6	0.806
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP011009	Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence	117473-117503	6	0.806
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP011009	Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence	6086-6116	6	0.806
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP009691	Bacillus mycoides strain ATCC 6462 plasmid pBMX_1, complete sequence	178151-178181	6	0.806
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP011009	Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence	10876-10906	7	0.774
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP011009	Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence	16820-16850	7	0.774
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP011009	Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence	35530-35560	7	0.774
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP011009	Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence	111059-111089	7	0.774
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NC_011973	Bacillus cereus Q1 plasmid pBc239, complete sequence	160771-160801	7	0.774
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP015507	Bacillus oceanisediminis 2691 plasmid pBO1, complete sequence	3988-4018	7	0.774
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NC_018688	Bacillus thuringiensis MC28 plasmid pMC319, complete sequence	223738-223768	7	0.774
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP016589	Bacillus thuringiensis strain KNU-07 plasmid pBTKNU07-01, complete sequence	365432-365462	7	0.774
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	CP016195	Bacillus thuringiensis serovar coreanensis strain ST7 plasmid pST7-1, complete sequence	284668-284698	7	0.774
NZ_CP017704_2	2.1|1389070|32|NZ_CP017704|CRISPRCasFinder	1389070-1389101	32	MT758689	Lactobacillus phage Lbab1, complete genome	104389-104420	8	0.75
NZ_CP017704_2	2.1|1389070|32|NZ_CP017704|CRISPRCasFinder	1389070-1389101	32	NC_012530	Lactobacillus phage Lb338-1, complete genome	108018-108049	8	0.75
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP017081	Bacillus muralis strain G25-68 plasmid pG25-68, complete sequence	36686-36716	8	0.742
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP040783	Bacillus thuringiensis strain HM-311 plasmid p1, complete sequence	235764-235794	8	0.742
NZ_CP017704_3	3.1|4909207|31|NZ_CP017704|CRISPRCasFinder	4909207-4909237	31	NZ_CP029455	Bacillus cereus strain FORC087 plasmid pFORC087.1, complete sequence	180307-180337	9	0.71

1. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NC_013793 (Bacillus pseudofirmus OF4 plasmid pBpOF4-02, complete sequence) position: , mismatch: 4, identity: 0.871

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
tcattttcttattcaactaacgggtgcgtta	Protospacer
 * *********  *****************

2. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP043831 (Bacillus sp. BS98 plasmid unnamed1) position: , mismatch: 6, identity: 0.806

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
tttaattcttattgaactaacgggtgcttta	Protospacer
 .*  ******* ************** ***

3. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP017081 (Bacillus muralis strain G25-68 plasmid pG25-68, complete sequence) position: , mismatch: 6, identity: 0.806

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
gctttttcttgtggaactaacggggcaggtt	Protospacer
**********.*************   * * 

4. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP017081 (Bacillus muralis strain G25-68 plasmid pG25-68, complete sequence) position: , mismatch: 6, identity: 0.806

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
tctttttcttatggaactaaaggggcagttt	Protospacer
 ******************* ***   *** 

5. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP017081 (Bacillus muralis strain G25-68 plasmid pG25-68, complete sequence) position: , mismatch: 6, identity: 0.806

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
gataagtcttattgaacgaacgggtgcgtta	Protospacer
* *   ****** **** *************

6. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP033045 (Bacillus foraminis strain Bac44 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.806

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
gctttttcttatggtactaacggggcaggtt	Protospacer
************** *********   * * 

7. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP011009 (Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence) position: , mismatch: 6, identity: 0.806

gctttttcttatggaactaacgggtgcgtta-	CRISPR spacer
cctttttcttatggtactaacggg-gcaggat	Protospacer
 ************* ********* **.  * 

8. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP011009 (Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence) position: , mismatch: 6, identity: 0.806

gctttttcttatggaactaacgggtgcgtta-	CRISPR spacer
cctttttcttatggcactaacggg-gcaggat	Protospacer
 ************* ********* **.  * 

9. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP011009 (Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence) position: , mismatch: 6, identity: 0.806

gctttttcttatggaactaacgggtgcgtta-	CRISPR spacer
gctttttattatggaactatcggg-gcagaat	Protospacer
******* *********** **** **.  * 

10. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP009691 (Bacillus mycoides strain ATCC 6462 plasmid pBMX_1, complete sequence) position: , mismatch: 6, identity: 0.806

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
tctttttcttatggcactaacgggggattga	Protospacer
 ************* ********* *  * *

11. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP011009 (Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence) position: , mismatch: 7, identity: 0.774

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
cctttttcttatggcactaacggggcagatt	Protospacer
 ************* *********   * * 

12. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP011009 (Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence) position: , mismatch: 7, identity: 0.774

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
cctttttcttatggtactaacggggcaggtt	Protospacer
 ************* *********   * * 

13. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP011009 (Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence) position: , mismatch: 7, identity: 0.774

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
gctttttattatggaactatcggggcaggtt	Protospacer
******* *********** ****   * * 

14. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP011009 (Bacillus simplex strain SH-B26 plasmid pSHB26, complete sequence) position: , mismatch: 7, identity: 0.774

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
cctttttattatggaactatcggggcagttt	Protospacer
 ****** *********** ****   *** 

15. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NC_011973 (Bacillus cereus Q1 plasmid pBc239, complete sequence) position: , mismatch: 7, identity: 0.774

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
aataattcttattgaactaacgggtgcattt	Protospacer
. *  ******* **************.** 

16. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP015507 (Bacillus oceanisediminis 2691 plasmid pBO1, complete sequence) position: , mismatch: 7, identity: 0.774

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
cctttttcttattggactaacggggcagttt	Protospacer
 *********** *.*********   *** 

17. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NC_018688 (Bacillus thuringiensis MC28 plasmid pMC319, complete sequence) position: , mismatch: 7, identity: 0.774

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
tctttttcttatgtcactaacgggggattga	Protospacer
 ************  ********* *  * *

18. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP016589 (Bacillus thuringiensis strain KNU-07 plasmid pBTKNU07-01, complete sequence) position: , mismatch: 7, identity: 0.774

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
tctttttcttatggcactgacgggggattga	Protospacer
 ************* ***.***** *  * *

19. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to CP016195 (Bacillus thuringiensis serovar coreanensis strain ST7 plasmid pST7-1, complete sequence) position: , mismatch: 7, identity: 0.774

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
tctttttcttatggcactgacgggggattga	Protospacer
 ************* ***.***** *  * *

20. spacer 2.1|1389070|32|NZ_CP017704|CRISPRCasFinder matches to MT758689 (Lactobacillus phage Lbab1, complete genome) position: , mismatch: 8, identity: 0.75

-tacactgaaatacccataagttttattacaaa	CRISPR spacer
ggatagt-aaatacccataagttctaatacatc	Protospacer
  *.* * ***************.** ****  

21. spacer 2.1|1389070|32|NZ_CP017704|CRISPRCasFinder matches to NC_012530 (Lactobacillus phage Lb338-1, complete genome) position: , mismatch: 8, identity: 0.75

-tacactgaaatacccataagttttattacaaa	CRISPR spacer
ggatagt-aaatacccataagttctaatacatc	Protospacer
  *.* * ***************.** ****  

22. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP017081 (Bacillus muralis strain G25-68 plasmid pG25-68, complete sequence) position: , mismatch: 8, identity: 0.742

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
cctttgtcttatggaactatcggggcaggtt	Protospacer
 **** ************* ****   * * 

23. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP040783 (Bacillus thuringiensis strain HM-311 plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.742

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
tagtgattttatccaactaacgggtgcgtta	Protospacer
   *  *.****  *****************

24. spacer 3.1|4909207|31|NZ_CP017704|CRISPRCasFinder matches to NZ_CP029455 (Bacillus cereus strain FORC087 plasmid pFORC087.1, complete sequence) position: , mismatch: 9, identity: 0.71

gctttttcttatggaactaacgggtgcgtta	CRISPR spacer
taggtaagttattgaactaacgggtgcttta	Protospacer
    *   **** ************** ***

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	2165397 : 2173692	8	Synechococcus_phage(50.0%)	NA	NA
DBSCAN-SWA_2	3190835 : 3199965	8	Staphylococcus_phage(66.67%)	NA	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP017704|2165397:2173692|DBSCAN-SWA
ATTAAGTAAGTTTCTTGTGGCATAGCTCCTGCAAAACTGACGGATACAAGTCATGCTCCATTTCCTGAATTCTTTTTTGAAGGATATCTTTCGTATCCCCCTCAAGAATTGGCACTGCTTTTTGGGCAATGACCGGTCCTGTGTCCATTCCATCATCAACATAATGAACCGTTACCCCCGTTTCCTTCACTCCGGCGTCAAAAGCCTGGCCAATTGCATCCTTGCCTGGAAAACTAGGCAAGAGTGAAGGGTGGATGTTCACAATCCTCTGTGAATACTTTTGTAATAATGTCGGACCGATCAAACGCATATAACCAGCCAGAATGATAAATTCTATCTCATACTGGCGAAGTTTTTCCAGGATTTCCGATTCATACTCAGTCTTGTTAGAGTAATTCTTCGCTAAAAAGGAGAAAGAATCAATATTCTCAAGCTTAGCTCTCTCAAGCACATATGCGTCTTCACGATCGCAAACGACAAGACAGATTTCCGCTTCCAACTTTCCACTTTTTATTGCTTCAGCAATTGATTGAAAATTACTACCGTTACCTGATGCAAAGACAGCAAGGCGTTTCATTATTTGAACGACACTCCATTTCCATCCACAACCGTTCCAATAACTGAGGCTTCTTCACCGCAAGACTGTAGGTGGGCTAGCACATCTGATGCCACTTCTTTTTTCACGACAGCCGTCATTCCAATCCCCATATTGAAGATATTGAACATTTCCTCTTTTACAAGGTTCCCTTTTTCTTCAAGGAATGAGAATATAGTTGGAATTTCCCAGCTTCCAAGCTCGATTTCAACACCGCATCCTTCAGGAAGAATACGCGGAATATTCTCGATGAACCCTCCACCAGTGATATGGGCAAGACCATTAACATCAAATTTTTCCAACGTCGATAAAACGGACTTCACATAGATTTTTGTCGGTTTTAATAATTCCTCTCCCAACTTGCAATCCAGTTCCGGTACGAAGTCATGAAGCGACATACCTGAGTCTTCAAGAAGAATTTTACGAACAAGGGAATACCCGTTACTGTGGATGCCGCTTGAAGCGAGTCCAATAACGACATCACCCGCCGAGATCGCTTCACCAGTAATTAGACGTGATTTTTCAACGGCACCTACAGTAAAACCTGCCACATCGTATTCTTCCGTCTCGTACATGCCTGGCATTTCAGCTGTTTCTCCGCCGATTAAAGCACATCCCGCCTGCTCACAGCCATCTGCAATCCCTTTGACGATCATTTCAATTCGTTCAGGATCTGCTTTACCGCAGGCAATATAATCTAAAAAGTATAAAGGTGCAGCACCTTGAACGACAACATCATTGACGCACATAGCTACACAATCCACTCCAATTGTATCGTGTTTATCCATCATGAACGCCAACAAAAGTTTCGTACCCACTCCATCCGTACCTGAAATGAGGACAGGTTCTTTAAGGTTCAAGGAAGATAAATCAAACATGCCGCCGAAACCGCCAAGACCATTCATTACTTCTGGACGTAATGTGCGCTTTACATGTTTTTTCATTCGATTTACCGCTTCATAACCAGCCTCAATATCCACACCAGCCTGTTTATATGCATTAGCCATTTGAAATCCTCCTCCGAAAATCAATCATCATTGCCGACTTGATTAACATTTTGTTTTTTCTCGTTCGTATTCAAAAATTTCAGTCGGATAATTTCCGGTGAAACAAGCTAGGCATGAACCGCGCGTTTCTCCAGGAAACGGTCGTCCAATTGCTTCGACCATACCTTCGACACTTAAAAAAGTTAAGGAATCAGCACCGATGATTTCTCTTATTTCCTCCACTGATTTAGAGCTCGCAATCAGTTCTTCCTTTTTAGACGTGTCAATGCCATAAAAACATGGATTCTTAATCGGTGGTGAGCTGATTACTACATGCACTTCTTTCGCTCCAGCATCTTTTAACATGCGGACAATCCTTCTGCTCGTTGTCCCACGGACGATTGAATCATCAACCATTATGACCCGCTTACCTTCCACTACCCCTCTTACAGGTGAAAGTTTCATCTTCACGCCTTGTTCACGCAAACTTTGTGATGGCTGAATGAACGTCCGTCCAACATACCGATTTTTTATTAAACCCATTTCATATGGAATGCCTGCAGCTTCAGCATAGCCAATCGCTGCCGAAATGCTGGAATCAGGTACACCTGTAACTACATCGGCTTCAATTTTGGTTTCCAGTGCCATTTGCTTGCCAAGATTTTTTCGTGCCGTATGAACATTGATCCCATCAATGTTGCTATCCGGACGGGAAAAATACACGTACTCCATCGTGCACATTGCCTGTTGACTGGAAAGCGAAAAGTATTCGGATGTGATTCCCTCATCATTAATGACAACCAGTTCACCCGGTTCAATATCGCGGATGAATTCTGCACCTACAATATCAAGTGCACATGTTTCGGATGCAGCGAAATATGCATCGCCTATTTTCCCCAAGGAAAGTGGACGGAAGCCATGCGGATCTCTAGCCATGATCATTTGGTTTTCTGTCATGATGACAAAGGCATAAGCTCCCTTCAGCATGCTTAAACTGTTCTTCACGGAATCTCTGATATCCGAGTAGCCGGAACGTTTAATCAGATGGGCCAGAACTTCCGTATCAGATGTCGTTTGAAAAATGCTTCCCTGTCCTTCAAGCTGTGCTTTTAACTGATGGGCATTGACGATATTCCCATTATGAGCAAGAGCCAGCCCTCCTGTATGTGAATTGAACAAGAAAGGCTGAACATTTTGATACCCGCCGCCGCCTGCCGTTGTATAACGGACATGGCCGATTGCTGCTTTTCCGGTACCGGAAAGTGCCTGCATTTTTTCTGCCGTGAATATCTCTGTGACAAGACCTTCACCCTTGGAGATTGACATCTGCTCACCGTCCGTCACGACGATGCCAGCTCCTTCTTGCCCACGATGTTGTAAGCTATGCAAACCGTAGTAAGCCAGCTGTGCTGCATCGGGATGTCCCCAGACTCCAACAACACCACACTCTTCGTTTAGGCTTCTTATTTCAGCAAGCATGGTATGGCTCCCTTCCAAGCTGTTTGTAAATCTTCAACGTCCGCTTCCAATACTTTGCTATCAATGTCTGTTGCCACGACTAATTTATTATCTCCCGTTACTGAGCCAATGCATATCGCATCTTCAACTAGCGCTTCGAATGCCGTTTTGTTTTCAGGCTTGATGGATAGTAGGAATCGAGATTGCGTTTCACTGAATAATTCTGATACCGGTTCGCCCGCTAAATTCACTTTTGCCCCAAGCTTGCTAGCCCCGAATAAAGATTCAGCTAAAGCCACTGCCAAACCGCCTTCCGAAAGGTCATGGGCTGATGCAACAAGTCCTTTTTGGATTGCAGCGAGGATTTGCTGCTGACGTTTTTGTTCAACGGCCAAATCAAGTTCTGGAGCGCGTCCAAAGATTTTACCCTCAAGCATTTTCTGTAATTCACTGCCACCAAATTCAACTTTCGCTTCGCCGACCACATAAATCAAATCGGATTCATTTTTAAATGTTTGTGTAGTGATGTGCTGAAGGTCACTGACAAGACCAACCATCCCAACTACAGGTGTCGGATAAATCGCTTCACCATTCGTTTCATTGTAAAGGGAGACATTTCCGCCAATTACAGGAGTACTTAAGCTTCTGCAAGCTTCACTCATACCGTCTGCCGCTTTTTCCAATTGCCAAAATATTTCAGGTTTTTCTGGATTCCCAAAATTCAAGCAATCCGTAATCGCTAAAGGTTCTGCACCCGAGCAAATGATGTTACGGGCAGCTTCAGCCACTGCGATTTTGCCACCTGTTTCAGGATCTAAATAAATAAAGCGGGAGTTGCAATCCGTCGTCATGGCAAGGGCCTTATTTGTACCCCGTACACGCACAACCGCTGCATCCGATCCAGGTGAGACGACTGTATTCGTGCGGACCATGTAATCATATTGGTCGTAGACCCATTCCTTACTCGAAATTGTCGGTTGCTTCAATAGTGATACCAATGTTTCTTTATAATCTCCAATGACTGGCACTTCTGCTGTCATGCTTTGGAAGTCACGGAAATATTGCGGTTCTGCAGATGGCTTGTGGTAAATCGGAGCTTCTTCAGCCAATGCATCAACCGGAACCTCAGCAACGATTTCACCTTGATGGGAAAGTGTTAGATTTTTATCATCCGTTACTACTCCAACAGCAACCGCTTCTAGGTCATATTTCGTAAACAAGTCAACGATTTCCTGTTCGCGTCCTTTAGTTACAACGATCAGCATCCGCTCTTGTGATTCAGAAAGCATCATTTCATATGCTGTCATTCCCGTTTCACGCTGCGGTACCAAATCAAGGTTCATTTTTATTCCTGATCCAGCTTTGCTCGCCATTTCGGCAGATGAACTTGTAAGACCCGCAGCTCCCATATCCTGAATACCAACAAGGGCATCATTTTGAATCAATTCAAGGCATGCTTCCAAAAGCAGTTTCTCCATGAATGGATCGCCTACTTGTACGGCAGGTCGTTTTTCTTCTGAAGACTCTGATAGCTCTTCAGATGCAAATGTTGCTCCATGAATACCATCACGTCCAGTTTTGGCACCCACATACATCACTGTGTTTCCCACTCCATGCGCTTGGCCTTTTTTAATGTCCTTATGATCGATCAAACCGACACACATTGCATTGACCAGAGGATTTCCTTCATACGATGGATCAAATTGAATTTCTCCGCCGACAGTTGGAATTCCGATACAATTCCCGTATCCTGCAATCCCTGCAACCACTTCTTTGAATAGATATTTCACACGATCATTGTCTAACTCACCGAAGCGAAGCGAGTTCAGCATCGCAATCGGACGGGCACCCATGGAGAAAACATCACGGATAATACCGCCGACACCAGTAGCAGCACCTTGATAAGGTTCAATTGCCGATGGGTGGTTATGACTTTCTATTTTAAAAACGACAGCCTGGTCGTCACCGATATCAACGATACCTGCTCCTTCACCAGGACCTTGTAGCACTTTCTCCCCTGTAATCGGGAACTTCCTTAAGATGGGTTTTGAATTTTTGTAGGAACAATGCTCTGACCACATAACCGAAAACAATCCAGTTTCCGTATAATTCGGCAGTCTGCCTAAGATTTTCTCAACCATTGCAAATTCATCATCGGATAGTCCCATAGTTGCGTACAATCGATCCGATTTAATTTTTTCCGGACTTGGTTCAAGCTGTAATAACATGTGATTCCCTCCAGTTTTTTACGATGGATTGAAAAATCTTTAAGCCGTCTTTACTGCCAAGCAGCGAATCAACAGCACGTTCGGGATGAGGCATCATTCCGAGGACATTTCCTTGTTCATTTGTAATTCCCGCTATTTGTTCCAAGCTTCCGTTTGGATTTTCACCATCATACGTGAACAAGATGCGGTTGTTTCGTTTTAATTCAGCCAATGTCTCATTATCACAGTAGTAATTCCCTTCACCATGGGCAACTGGAATCGTAATCGTTTCATTTAATTCATATCCTGTCGTGAACATCGATTGATTATTTTCAACCTTCAATCCTACATTGCGGCAAATGAATTTCAAGCCTTCATTACGGCGCATCGCTCCAGGTAAAAGTCCTGCTTCAAGTAAAATCTGAAAACCATTGCAGACACCCAATACAGGCTTTCCTGCTTGTGCCGCTTTTACGACTTCGGCCATTACATTCGAAAATCGTGCAATTGCTCCAGAGCGTAAATAGTCTCCATAAGAGAAACCTCCAGGAAGGAGAATCCCATCATACTGATCTAGATTGTCTGTAGAGTGCCAAACATACTCCACTTCTTCCCCAAGTGCATCCTTTATCGCATGGTACATATCGACATCACAATTGGAACCAGGGAAAACTATGACAGCAAATTTCATTGGGTGATAACCTCCTCAACATCATAACGGTAAGCTTCAATTACCGTATTGGCCAATAGTTTTTCACACATTTCCTTCACAAGTTGATCTAAATCACGATCCGTATCCTTAATTGTAAGTTCAATGTATTTCCCCACTCGAACATCACTAACTTCGTTATAAGTCAAACTATGAAGTGATTGTTGCACTGCTGCTCCCTGTGGATCTAGTACACTTTCGCGTAGTGTGATATATACCTTAACCTTATACATGTTGAGTGCCCTCCAACTTTGCTAGTATTTTTTCGTAAGCATCTGTTAAACTGCCTAAATTACGGCGGAATACATCTTTGTCTAACTTTTCGTTCGTGTTAATATCCCATAATCGGCAGGTATCAGGTGAAATTTCATCTGCCAGCAGAATGTCTCCATTCGGGGTTTTACCGAACTCTAATTTAAAATCAATCAATTTAATGTCCAATTCTTTAAAGAAGGAAGTTAAGACGATACTGATTTCTTGTGCCTTTTCTTTTAAAATGGCTACATCTTCCTTGCTTGCAAGTTCCAATTCTTCAATATGGTCTTCCGTTAACAGAGGATCGCCGAGCTCGTCGTCTTTATAGTAAAACTCAATCAGCGTTTTCTTGAGCGGCTGGCCTTCTTCAATGCCAGTCCTTTTAGAAAAACTGCCGGCAGCCGTATTTCTGACAACGACTTCAAGCGGAATGATGGATACCCTCTTGACTAGCTGCTCCCGGTCGGAAAGCTTTTCAATAAAATGGGACGGGATATTTTCCTGGGCAAGCTTTGAAAAGAGTAAGCTAGTAATTTGATTATTCAACTTACCTTTTCCGGCAATCTCTGACTTCTTCTCACCATTAAACGCTGTTGCCGAATCCTTGTATTCCACCCATACTATTTCACTGTTGTCCGTTGCAAAAATCTGTTTCGCTTTTCCTTCATACAACAATTCTCGTTTTTCCATCTGTCCAGACCCCCACATTGTGAATATTATGAATCTTCCTGCCATTGATCAGGCTTGGCAAACATATCACCGTTTAGAGGTGCCATGTTTGCCGCCTTCACTTTTATAAACCTAAACGATCAAAGATTACATCAACATTTTTCAGGTGATGTGTAGGATCGAAACAATCATCAAGTTCTTCTTTCGTAAGCAAGCTTGTGATTTTATCATCCTTTTCGATCAGGCTTCTGAATGGAACCTGAAGCTCCCATGCTTCCATCGCTTTCGGCTGAACCGTATCATAAGCTTCTTCACGGACAAGTCCTTTATCGATAAGGGAAAGCAGCACACGTTGTGAGAAAATCAATCCCAGCGTACGGTCCATATTGCGTTTCATATTTTCTGGATAAACGGTCAAGTTCTTAATTATGTTGCTGAAACGGTTCAGCATGTAGTTTAATGCGATCGTTGCATCCGGCAAGATGATGCGCTCAGCAGAAGAATGAGATATGTCACGTTCATGCCATAATGGCACATTCTCATATGCTGTCATCATGTAACCGCGGATTACACGAGCCATACCCGTCATATTTTCTGAGCCGATTGGATTCCGTTTATGAGGCATTGCCGAAGATCCCTTTTGTCCTTTTGCAAAGAATTCTTCCACTTCGCGTGTTTCACTTTTTTGCAAGCCGCGAATTTCCACTGCGAACTTTTCAATTGATGTCGCAATTAAAGCCAATGTGCTCATATAATGTGCGTGGCGATCGCGCTGCAATGTTTGCGTTGAAATAGGCGCTGCCTCAAGGCCAAGCTTTTCACAAACGAATTTTTCAACGAACGGGTCGATGTTAGCGTAGGTTCCGACAGCTCCAGAGATTTTCCCAACCTCTATGTTCTTTCTAGCTTCTTCAAAACGTTCGACATTTCGTTTCATTTCTTGATACCAAAGTGCCAGTTTCAACCCAAAAGTGGTCGGTTCAGCATGAACTCCATGTGTACGTCCCATTTGAACCGTGTATTTATGTTCTTTCGCTTTATTTTTCAGGATCTCCACGAAGTTATTTAAATCCTTGGCAAGGATATCATTCGCTTGCTTTATTACATATGAAAGAGCTGTATCCACCACATCAGTAGAAGTCAGTCCGTAATGGACCCATTTCCGTTCTTCACCCAACGTTTCAGAAACCGCACGTGTAAAAGCAACAACATCGTGGCGTGTATCTTTTTCGATTTCATTGATACGGTCCACATCGAATGTAGCATTTTCACGAAGAAGCTTCACATCTTCTTTTGGAATGACACCTAGTTCAGACCATGCTTCACAAGCTAAGATTTCAACTTCCAACCACGCATTAAAGCGGTTCTTTTCTGTCCAAATGTTTCCCATCTCTGGGCGGGTATAACGTTCAATCAT

Protein sequences of DBSCAN-SWA_1

>NZ_CP017704|2165397:2173692|2170646_2171333_-|WP_034306116.1|DBSCAN-SWA
MKFAVIVFPGSNCDVDMYHAIKDALGEEVEYVWHSTDNLDQYDGILLPGGFSYGDYLRSGAIARFSNVMAEVVKAAQAGKPVLGVCNGFQILLEAGLLPGAMRRNEGLKFICRNVGLKVENNQSMFTTGYELNETITIPVAHGEGNYYCDNETLAELKRNNRILFTYDGENPNGSLEQIAGITNEQGNVLGMMPHPERAVDSLLGSKDGLKIFQSIVKNWRESHVITA
>NZ_CP017704|2165397:2173692|2171576_2172296_-|WP_063235720.1|DBSCAN-SWA
MEKRELLYEGKAKQIFATDNSEIVWVEYKDSATAFNGEKKSEIAGKGKLNNQITSLLFSKLAQENIPSHFIEKLSDREQLVKRVSIIPLEVVVRNTAAGSFSKRTGIEEGQPLKKTLIEFYYKDDELGDPLLTEDHIEELELASKEDVAILKEKAQEISIVLTSFFKELDIKLIDFKLEFGKTPNGDILLADEISPDTCRLWDINTNEKLDKDVFRRNLGSLTDAYEKILAKLEGTQHV
>NZ_CP017704|2165397:2173692|2167040_2168456_-|WP_063235722.1|DBSCAN-SWA
MLAEIRSLNEECGVVGVWGHPDAAQLAYYGLHSLQHRGQEGAGIVVTDGEQMSISKGEGLVTEIFTAEKMQALSGTGKAAIGHVRYTTAGGGGYQNVQPFLFNSHTGGLALAHNGNIVNAHQLKAQLEGQGSIFQTTSDTEVLAHLIKRSGYSDIRDSVKNSLSMLKGAYAFVIMTENQMIMARDPHGFRPLSLGKIGDAYFAASETCALDIVGAEFIRDIEPGELVVINDEGITSEYFSLSSQQAMCTMEYVYFSRPDSNIDGINVHTARKNLGKQMALETKIEADVVTGVPDSSISAAIGYAEAAGIPYEMGLIKNRYVGRTFIQPSQSLREQGVKMKLSPVRGVVEGKRVIMVDDSIVRGTTSRRIVRMLKDAGAKEVHVVISSPPIKNPCFYGIDTSKKEELIASSKSVEEIREIIGADSLTFLSVEGMVEAIGRPFPGETRGSCLACFTGNYPTEIFEYEREKTKC
>NZ_CP017704|2165397:2173692|2165397_2165973_-|WP_063235724.1|DBSCAN-SWA
MKRLAVFASGNGSNFQSIAEAIKSGKLEAEICLVVCDREDAYVLERAKLENIDSFSFLAKNYSNKTEYESEILEKLRQYEIEFIILAGYMRLIGPTLLQKYSQRIVNIHPSLLPSFPGKDAIGQAFDAGVKETGVTVHYVDDGMDTGPVIAQKAVPILEGDTKDILQKRIQEMEHDLYPSVLQELCHKKLT
>NZ_CP017704|2165397:2173692|2172399_2173692_-|WP_063235719.1|DBSCAN-SWA
MIERYTRPEMGNIWTEKNRFNAWLEVEILACEAWSELGVIPKEDVKLLRENATFDVDRINEIEKDTRHDVVAFTRAVSETLGEERKWVHYGLTSTDVVDTALSYVIKQANDILAKDLNNFVEILKNKAKEHKYTVQMGRTHGVHAEPTTFGLKLALWYQEMKRNVERFEEARKNIEVGKISGAVGTYANIDPFVEKFVCEKLGLEAAPISTQTLQRDRHAHYMSTLALIATSIEKFAVEIRGLQKSETREVEEFFAKGQKGSSAMPHKRNPIGSENMTGMARVIRGYMMTAYENVPLWHERDISHSSAERIILPDATIALNYMLNRFSNIIKNLTVYPENMKRNMDRTLGLIFSQRVLLSLIDKGLVREEAYDTVQPKAMEAWELQVPFRSLIEKDDKITSLLTKEELDDCFDPTHHLKNVDVIFDRLGL
>NZ_CP017704|2165397:2173692|2168440_2170663_-|WP_063235721.1|DBSCAN-SWA
MLLQLEPSPEKIKSDRLYATMGLSDDEFAMVEKILGRLPNYTETGLFSVMWSEHCSYKNSKPILRKFPITGEKVLQGPGEGAGIVDIGDDQAVVFKIESHNHPSAIEPYQGAATGVGGIIRDVFSMGARPIAMLNSLRFGELDNDRVKYLFKEVVAGIAGYGNCIGIPTVGGEIQFDPSYEGNPLVNAMCVGLIDHKDIKKGQAHGVGNTVMYVGAKTGRDGIHGATFASEELSESSEEKRPAVQVGDPFMEKLLLEACLELIQNDALVGIQDMGAAGLTSSSAEMASKAGSGIKMNLDLVPQRETGMTAYEMMLSESQERMLIVVTKGREQEIVDLFTKYDLEAVAVGVVTDDKNLTLSHQGEIVAEVPVDALAEEAPIYHKPSAEPQYFRDFQSMTAEVPVIGDYKETLVSLLKQPTISSKEWVYDQYDYMVRTNTVVSPGSDAAVVRVRGTNKALAMTTDCNSRFIYLDPETGGKIAVAEAARNIICSGAEPLAITDCLNFGNPEKPEIFWQLEKAADGMSEACRSLSTPVIGGNVSLYNETNGEAIYPTPVVGMVGLVSDLQHITTQTFKNESDLIYVVGEAKVEFGGSELQKMLEGKIFGRAPELDLAVEQKRQQQILAAIQKGLVASAHDLSEGGLAVALAESLFGASKLGAKVNLAGEPVSELFSETQSRFLLSIKPENKTAFEALVEDAICIGSVTGDNKLVVATDIDSKVLEADVEDLQTAWKGAIPCLLK
>NZ_CP017704|2165397:2173692|2171329_2171584_-|WP_034306118.1|DBSCAN-SWA
MYKVKVYITLRESVLDPQGAAVQQSLHSLTYNEVSDVRVGKYIELTIKDTDRDLDQLVKEMCEKLLANTVIEAYRYDVEEVITQ
>NZ_CP017704|2165397:2173692|2165972_2166998_-|WP_063235723.1|DBSCAN-SWA
MANAYKQAGVDIEAGYEAVNRMKKHVKRTLRPEVMNGLGGFGGMFDLSSLNLKEPVLISGTDGVGTKLLLAFMMDKHDTIGVDCVAMCVNDVVVQGAAPLYFLDYIACGKADPERIEMIVKGIADGCEQAGCALIGGETAEMPGMYETEEYDVAGFTVGAVEKSRLITGEAISAGDVVIGLASSGIHSNGYSLVRKILLEDSGMSLHDFVPELDCKLGEELLKPTKIYVKSVLSTLEKFDVNGLAHITGGGFIENIPRILPEGCGVEIELGSWEIPTIFSFLEEKGNLVKEEMFNIFNMGIGMTAVVKKEVASDVLAHLQSCGEEASVIGTVVDGNGVSFK

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_063235724.1|2165397_2165973_-	phosphoribosylglycinamide formyltransferase	M4QRX9	Synechococcus_phage	1.4e-28	37.7
WP_063235723.1|2165972_2166998_-	phosphoribosylformylglycinamidine cyclo-ligase	A0A0E3F760	Synechococcus_phage	6.0e-67	45.9
WP_063235722.1|2167040_2168456_-	amidophosphoribosyltransferase	A0A0M3SGR2	Mollivirus	8.6e-56	34.0
WP_063235721.1|2168440_2170663_-	phosphoribosylformylglycinamidine synthase subunit PurL	A6N228	Microbacterium_phage	2.5e-166	43.1
WP_034306116.1|2170646_2171333_-	phosphoribosylformylglycinamidine synthase subunit PurQ	NA	NA	NA	NA
WP_034306118.1|2171329_2171584_-	phosphoribosylformylglycinamidine synthase subunit PurS	NA	NA	NA	NA
WP_063235720.1|2171576_2172296_-	phosphoribosylaminoimidazolesuccinocarboxamide synthase	A0A0E3HI61	Synechococcus_phage	2.2e-47	43.5
WP_063235719.1|2172399_2173692_-	adenylosuccinate lyase	A0A2H4UUU6	Bodo_saltans_virus	2.9e-18	24.4

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP017704|3190835:3199965|DBSCAN-SWA
TATGAAACTTTGTACAATCGGACTTGGTTATATAGGACTTCCAACATCTTTAATGTTTGCGAAACACGGTGTCGATGTTGTCGGCGTGGATATCCATCCTGAGATTATTTCCAATTTGAATAGCGGCAGGCTCCATATCGAAGAACCTGGATTGGATGAGGTATTAGAAGAAGTGATTACTTCCAATAAGTTCCGAGCTGCGTTAAGCCCGGAACATGCGGATGTTTTCATTATCGCGGTGCCTACTCCAAATAAAAAGGACATGCATCAATCCTGTGATTTAACTCATGTCATGGATGCAACCTCCAACATTCTTCCTTTCATCAAAAAAGGGAATGTCATCATTATCGAATCGACGATTGCGCCAAGAAGCATGGATGATCATATTAGACCGATGATCGAGAGGACGGGCCTTACCATCGGAAAGGACATTTTCCTCGTTCATTGTCCGGAACGTGTTTTACCTGGAAGGATTCTTGAAGAGTTGGTTCATAATAACCGTATCGTCGGGGGCATCACGGAAACATGCTCATATAAAGGAAGTCTTGTTTACAAAACCTTTGTTCAGGGGGAGATCATTCAGACGGATGCGAAAACGGCTGAAATGTCCAAACTGATGGAAAACACTTTCAGGGATGTTAATATCGCCCTTGCGAATGAGCTGACGAAAGTCTGTTTCGAACTGGACATCAATGTTTTGGATGTCATATCAATGGCAAACAAACACCCTCGAGTCAATATACACCAACCAGGACCAGGAGTTGGCGGCCATTGTTTAGCGGTCGATCCGTATTTCGTCGTTGCAAAGTCACCAGAGTATGCGAAAATCATTAAATTGGCCCGTGATACCAACGTATCGATGCCTTATTATATCGTTAATTGTGTAAGGATGATGCTAGAGGGGATCCGGAAGCCAAAAGTAGCTGTTTTCGGTCTTGCATACAAAGGAAATGTAGATGATATTCGTGAAAGTCCCGCCATTGATGTCGTCAATATCTTGATGGGGATGGAAAACATGGATGTAGCCTTGCATGACCCGCATGTCCAATCTGGAAAGATGCCAGTCGTATCAGTTGAAGACGCTGTAAATGATGCAGACTTGATACTTGTCCTGACTGACCATGATGAATTTAAACAGATGGATTATGATAAGCTATCGAATCTCATGAGCAATAAATTGATTTTGGATACACGCAATTGCATTGATGCAACTAAAACCGATGTACCGGTGGCCAACCTGGGCAATATATATCAATACAAAACGATGTCCATGAAAAAAGCCAGGAATAAAGCGATCATCTAAAAATTTGGACAGACATAGATAATGGAATAAGGATTAAGGGGGCGCTGACCATGACAGCGCCCTTTTTGAATATCATGATCTGACTGGAGGGACGGGCATTAAACCAATGAAGAAAAGGACCAAGCAAGAGCTTGGTCCTTTCAGAATGTAAAAGCGTTCCAGTTGGTTTCGGAAATCCGCTCCCTTTCCGCCAAGCCTCCTCGCCGAAAGCATCTAGCGGGGGCTTGGCTAGCCAGTTATTCGGCAGGAGTGTCGCAATTATCTTCAATCCAATAAGGATTACAGTAAAAAAACCATGTAGGATAACCTAGTCTTGGTTTAAAATCATGTTTCGGGAAGAAACATTTCTTGTCGAAAAACTTAAAGGACCAAGCAAGAGCTTGGTCCTTTTGTGTACAATTTATTGAGCTGTCGGTCCGCCAAGTTCTTCGATTTCACTTGGAACACTGCCGAATTTCTTGAAGTTTGCACGGAATTGAGCGGCGAGGGCTGTTGCTGCTTGTTTATAAGCGGCAGGATCTGCCCAAGTCTTGATTGGTTGAAGCACTTCGTCTGGAACCCCAGGAACATGAAGAGGAATATCCAAACCGAAGATTTCATCTTTGATCGTTTCGATGTTCGCTAATTCACCTTCAAGTGCCGCTTGTACCATCGCACGAGTGTAAGCAAGTTTCATACGGCTTCCAGTTCCGTATGCTCCGCCAGTCCATCCAGTGTTGACAAGGTATACCTTTGCATTGTGCTCGTCAATTTTATCACCAAGCATCTCAGCATAGCGTTGAGCGGGAAGCGGTAAGAAAGGTGAACCGAAGCAAGTGGAGAATGTAGCTTCCGGTGAAGTTACGCCTCTTTCAGTACCAGCCAATTTACTAGTGTATCCACTTAGGAAATGGAACATTGCCTGTTCTTTCGAAAGCTTGCTGATTGGAGGCAGAACGCCTGAAGCATCAGCTGTTAAGAAAATGATTGTATTAGGGTGTCCTGCAATACTTGGGTTCACGATGTTATCGATCGCTTGCATTTGGTAAGCAGCACGAGTGTTTTCAGTCAATGAACTGTCATCATAGTTCGCTTCACGTGTATCCGGATCAACAACAACATTTTCCAGTACGGCACCGAAACGGATCGCATCGAAAATTTGTGGTTCTTTTTCACGTGAAAGATTAATCGTTTTCGCATAGCAGCCGCCTTCGATGTTGAATACACCGTTAGAAGACCAGCCGTGCTCGTCATCACCAATCAGTTTACGACTAGTGTCTGCGGATAAAGTTGTTTTGCCTGTACCGGACAGTCCGAAGAATAAAGCGACGTCCCCTTCACGTCCTACGTTAGCAGAGCAATGCATTGGAAGGATTCCAGCCTCTGGAAGTAAGTAGTTCATGATCGAGAAGATCGATTTTTTCATTTCTCCTGCATATTCCGTTCCGCCGATCAGGATTGTACGGCGTTCAAATGAAACGATGATGAAAGTTTCGGATGAAGTTCCGTCCACTTCTGGGTCTGCTTTGAAGTTAGGTGCAGAAAGGATTGTGAATTCTGCTTCGTGACCTCTTAGTTCCTCTTCGTTTGGACGGATGAACAAAGTATGGGCGAAAAGGTTATGCCAAGCATATTCATTAACAACACGGATTGGAAGACGTGATGATTCGTCTGCACCAGCGAAACCTTTAAAAACAAAGATCTCTTCTTTTGCTTTTAGGTAGTCAACTACTTTATTATATAGTTTATTGAACACATCTTCGGAAATTGGCTGGTTCACTGAACCCCAATCAACTTTATCTTTAACTGATGCTTCTTCCACGATATATTTATCCTTAGGTGATCGACCAGTATATTTGCCAGTTTCAGCTTTTACCGCGCCGGTTGATGTTAAAACGCCTTCACTTCTGCTTAATACTTTTTCGACCAATTGAGGAACTGAAAGTTGAGTTTGCACATTGTTTCCTGTTAATAATTGGTGTAACTCATTAGAAACATCTACAGAATTCATATATGAGGTACCTTCCTTTGTTTAAGTTTTTAGATTACAATTAGTATAACACATTCATTTAATTAGTCTATACTATTTCTTTTAATTTGTGATTATTTTCAGTTGGTCGCGTTAATCATTTTAATCCGGCAGGAACCGAGTCAGGATTATCGCATATACTTTCATGAAGAAAATTTTATTTTAATAGGAAGTAAGTAAGCAATACATGTCTATTGGGAAAGTCAGGATGTCGTTCCTTTTCGTATGCTCAATACTTTATTATTAATGGCAATTTACAACATTTCTATTCGTATTTTGCATTGTAAACCCTTCTAGGACGTTGTATCAACATGTTTTTTTAAATGAACGCCATTCTGAGTGGAAATGTTCTTTTTAGAAAAGCATTGACAAATTCCAGCTAGATACGATAATATCTTAAATTGTACGGATTCTCTTATCCCGAGTTGGTGGAGGGACAGGCCCTTTGAAACCCAGCAACCTGCCATATTGAACTTGACTCCAAGATCGATCGCCGAAAATAAAGCGAAGGTCTTCAAGGAATAGTGGTGATGGTGCTAACCTGAGCAAGGTAAAAAACCCTTGAACGATAAGAGTGAAAGGATAGAAGACAGAATTTTAAACCTTTCCTCATTTGCCAGGGAAGGTTTTTGTGTTTTTTATAAGTAATTCTGTGTCTATAGTTGAAACTAATGAGGGAAACGAGTTCCGTAAAAAACAGGCTTATGCCTACAACATACTAACTTCCAAGGAGGAAATATGATGTCAAAGAAACGTCTATTTACTTCTGAATCTGTTACAGAGGGCCATCCGGACAAAATTTGTGATCAGATTTCAGATTCCATTTTAGATGCTATCCTTGCTAAGGATGCAAATGCACGTGTAGCGTGTGAAACTAGTGTAACAACAGGTCTTGTACTTGTTGCCGGTGAAATTACAACGTCCGCTTACGTGGATATTCCGCGTATCGTTCGTGATACGATTAAAGGAATTGGCTACACACGTGCGAAATACGGTTTCGATGCTGAAACTTGTGCCGTATTGAGTTCCATTGATGAGCAGTCTGCCGATATCGCAGCTGGTGTCGATAAAGCATTGGAAGCTCGTGAAGGAAACATGTCAGAGGAAGAAATCGATGCAATCGGTGCAGGGGACCAAGGTCTTATGTTCGGATTTGCTTGTAATGAAACAGAAGAGCTTATGCCGCTTCCGATTTCATTGGCGCATAAACTTTCATTCCGCTTGGCTCAAGTACGTAAAGATGAAACTCTTCCTTACTTACGCCCTGATGGTAAAACACAGGTAACTGTGGAGTATGATGAGAATAACCTTCCTGTACGTGTAGATACGATCGTTATCTCTACACAGCACGATGCAGAAATTACGCTTGAACAAATTCAAGCCGATCTAAAAGAACATGTGATCAAAGCAGTCGTTCCAGCTGAATTGATCGATGCTGAAACTAAGTACTTCATCAACCCGACTGGCCGTTTCGTAATTGGCGGACCTCAAGGTGATGCTGGTCTTACTGGACGTAAAATCATCGTTGATACTTACGGCGGATACGCTCGTCACGGCGGCGGTGCATTCTCTGGTAAGGATGCTACTAAAGTTGACCGTTCTGCTGCATACGCTGCTCGTTACGTTGCGAAAAACATCGTGGCAGCCGGCCTTGCCGACAAAGCGGAAGTTCAATTGGCATACGCAATCGGTGTGGCAGAGCCTGTATCAATCTCTATTGATACTTTCGGAACTGGTACAGTTAGCGAAGAAGTCCTTGTTGACTTAGTTCGCGCTAACTTCGACCTTCGTCCAGCTGGAATCATCAAAATGCTTGACCTTCGTCGCCCAATCTACAAACAAACAGCTGCCTACGGACACTTTGGCCGTACAGATGTCGATCTTCCATGGGAACGCACGGACAAAGCAGAAACATTAAAAGCACAAGCGTAATCCATAAAAAAAGGTGTCCCGCAATAGCGGGGCACCTTTTTTATGGATTAATTTTGCCGTCAGCGGGAATAATTCAAGAAATCCCAAAGAAATTCAAATTACGTGCAATACTCGTGAGTTAGGGGCGATTACAAGTTTGTTTGGGTCAACTACTAATGAGTTTGGAACTTTTACTCATGAGTTTGAGTACAATACTCGTAACTTTCAGTCAATTGCTCGTGAGTTACTTTATTCGTTCCGCCGTTTTATAGTATTGTCCTTTTTCGGCGTATTCGCGTACGATGCGTTCCATATCCTGGCGATCTTCTTCGTTGATTTCGCGAATGACTTTAGCTGGGCGCCCGAATGCCAACATGTTCGGTGGAATGACTTTACCTTGGGGAACGAGACTGCCGGCACCGATGAAGGCCCCTTCGCCGATTTCGGCTTCATCAAGTACAATCGATCCCATGCCGATCAAAGCTCCTTTACGGATTTTACAGCTATGTAAAATGACCTGGTGGCCAATGGTTACTTCATCCTCGATGATCAATGGATTATTTGGGCTTTGGTGCAGGACGCTGTTATCCTGTATACTGACTTTTTTCCCGATGATGGTTGGGGATACATCACCGCGAATGACGGAATTGAACCAAATTGATGTTTCGTCGCCAATTTTGACATCACCAGTCACGACAGCATTTTCAGCAATATAAGCGCTTTCAGCAATTTCAGGTTCTTTGCCTTTATACGGATAAATAATCATTTTCAATCATTTCCTTTCCGAAGTGAATGTTTTTATGTATTATTTTAATATACCGTATGCAAATACACTTGGCTATTTATAATAGCAATGTACAACTTGTTAGATTTCTTTTTTGTCGAAAATCACGAATATGGTTATAATTTATATATATTATTTTAACTATCATGGATCGTACACAACAAGTGAAAAGTGAAAGGGGGATTTCGAATGTGGAAATGGGAGACAGAAGGAGACGCAAAGGGCGTCATTGTCATCATTCATGGGGCAATGGAACATCACGGACGTTATAAGTGGGTAACACAAATGTGGCTTTCAGCTGGATACCATGTCGTCATGGGCGACCTTCCAGGGCAGGGTATGACAACTCGCGCCTACCGGGGACATATCGATTCCTTTGATGAGTATTTGGACGAAGTGAAAAGCTGGATAGAAGAGGCTTACGAATATTCGTTGCCGGTCTTTTTACTTGGACACAGCATGGGTGGTTTGATTTCGATACGCCTTCTTCAGGAAGAGGAATGGGACATTGCAGGGGTGATTCTTTCTTCTCCATGCTTGGGCCTCGTGACGAAGCCGCGGAAGTTCCTTACAACCATCTCGCATGGTTTGAACTTCGTGATGCCTATGTTCAGGGTAGATTCCGGATTGACACCTGAAATGGCGACGAGAAGTGCGGAAGTTCGTGAATCCGATAGAAACGATACATTATATATCACAAAGGTTTCGATTCGCTGGTATCGCGAGTTGGCACAGGCCATGAAGGATGCTTTTGAAGAGATTCCTGAATTTCAGGATGTGCCGCTTTTGGTCATGCAGGGCGGAGATGACCGAATCGTGAATAAGAAGGCGGTTCGTGAGTGGTTTAATTATAACTTGGCCAGTGAAAAGCAATATAAGGAATGGCCGAAGCTTTATCATGAAATCTTCAATGAACCAGAGCGTGATGATGTATTTCAATATGCGCTGAGTTTTGTTGAAAACCGTTTAAAGATTTTAGGGTATGTCGTTTGATCAGTACATACTGTCACGATAAATGAAAAAGCTGCCGAAGTTAGATCTCGGCGGCTTGTTTTTATTTGGTTCAGCCTGCGTTTTTAAGCATTTCATTCGATTTGATGACCGGTGCCCAGAAAGTAACCGGATACATAAATTGGTTTAAATGTGTAAGTTCTTTTTTATTGGATAATGCGATCGATAGAAGATAAATGGATTTGAAGGTCAAATCATTGGCGAATAGGTCCAAAAGCGTCGCTTTCATATTCATGATTGCTTCATGGTTTTGGGTGGAAATCATTAAATCGAGCTGTGGCAGGAACTTATCAAAATGATGATCGAATTGTTTGAGGTCCTCCATGGTTTTTTGTTTTTCTGTCAACGAGTTAAGCGAGCTGACAAAATTCCCGTATTGCTCACTTGAATTCCTTTTGATTTTTTCAGTCAGTATATCCGTCAGTATTGAAGTAGGCAAATGTTTCATTTTCTGCACCCTCTTATCTATTTTCTATCATTATAATCATTGTAGACGAAAAATTCAAAAAGTTATGATTGGTAATTCTGCTGCATGCGAGTGTGGATTGAAAAAACACCGTTCGTATAGAACGGTGTCAAAAGTCATCATCTCTTTTCAATCGCGACAATGAATGGCGGATTGTTTGCTTGGTTGATGAACCCGTATTTAAGGATATGGGCTTTCTGTTGAGGGAAGTTCTGTACATAATCCATCAATGCATCCCGTTCTGCCGATCCCCCTGGATGACCATGGTAAATGACGAGGATGATGATGCCTTCAGGCGCCAGCAATTCGAACAGCTGTTCAATGGCTGATATCGTCGTATCGGCTTGGGTGATGATTGATTTGTCTCCGCCAGGAAGGTAGCCTAGGTTGAAAATGGCACCCGTGATCTTTCCGGAATGTTCGTTCCTGATGTATTTGCTTAAATGTTCATGCCCATCGTGAATGAGGGTGCAGCGCTCTTGTAAATTCTCGGCGTTCAGTTTCGCCGTTGTGGTTTGGATCGCTTCTTCCTGAATATCAAAGCTATAGACATGTCCGTCTACACCTGTAAGTCCTGCAAGAAAGACCGTATCAAAGCCGTTGCCCATCGTCCCATCTATAGTTATATCCCCGGGGTGGACCGCTTTTTCCAGCAGAATCCTGGCGAATGGCAAAATTCGATCAAGCTTCATGATTGTACCTCCATGTGATGATTTTTCCCCTGCCAGCTGTTGCGGCGTTTCAATTCGGCGTCAATGGCATTCAAGACATCCCATTTATTGACGCTCCACATTGGACCGATCATCAAATCGATCGGACCGTCACCCGTAATGCGGTGAACGATCATTTCTGGAGGGATTATTTCCAGCTGGTCACATACCAGGCTGACATAATCGTCACGGTCAAGAAACTCGAGCAGGCCTTTTTCATATTGTTTGACCATCGGTGTCCCTTTTAATAAATGAAGTAAATGGATCTTTATCCCCTGCACATCGAGTTTGGCGACTTCACGGGCTGTTTCCATCATCATGCCGTAATCTTCCTGAGGAAGGCCATTAATGATATGGGAGCATACGCGGATGCCGTGTTTGCGCAGTTTGTCGACGCCTTCTTTGTAGCAATCGAAGTCATGGGCACGGTTGATCATCGTCGCTGTCTTTTCATGGACCGTCTGGAGACCTAGTTCCACCCAAAGGTAAGTGCGTTCGTTCAATTCCGCTAAATACTCGACCACATCTTCTGGAAGGCAATCCGGGCGCGTCGCGATCGAGAGTCCGACGACACCTTCCTGGGTCAATACACTTTCATATTTCTCACGAAGCTCTGCCACGGGTGCATGCGTATTCGTGAACGCTTGGAAATAGGCCATATATTTTCCATCTTTCCATTTATGATGCATCCGTTCGCTGATCTTCTTAAACTGGACGTCGAGGGGTTCAACCCTGCTGCCAGCAAAGTCACCAGAGCCTGAGGCACTGCAGAAGGTACAGCCGCCATGTGCGACGGTGCCATCACGGTTCGGACAGTCAAAACCGCCATCAAGAGCAACTTTAAAAACCTTATGACCAAAATGTTCCCTAAGGTGGTAATTCCATGTATGATATCGTTTGTTATCCGTTGCATATATAAACGGGTTTGCTTGATTCAA

Protein sequences of DBSCAN-SWA_2

>NZ_CP017704|3190835:3199965|3192537_3194127_-|WP_063234883.1|DBSCAN-SWA
MNSVDVSNELHQLLTGNNVQTQLSVPQLVEKVLSRSEGVLTSTGAVKAETGKYTGRSPKDKYIVEEASVKDKVDWGSVNQPISEDVFNKLYNKVVDYLKAKEEIFVFKGFAGADESSRLPIRVVNEYAWHNLFAHTLFIRPNEEELRGHEAEFTILSAPNFKADPEVDGTSSETFIIVSFERRTILIGGTEYAGEMKKSIFSIMNYLLPEAGILPMHCSANVGREGDVALFFGLSGTGKTTLSADTSRKLIGDDEHGWSSNGVFNIEGGCYAKTINLSREKEPQIFDAIRFGAVLENVVVDPDTREANYDDSSLTENTRAAYQMQAIDNIVNPSIAGHPNTIIFLTADASGVLPPISKLSKEQAMFHFLSGYTSKLAGTERGVTSPEATFSTCFGSPFLPLPAQRYAEMLGDKIDEHNAKVYLVNTGWTGGAYGTGSRMKLAYTRAMVQAALEGELANIETIKDEIFGLDIPLHVPGVPDEVLQPIKTWADPAAYKQAATALAAQFRANFKKFGSVPSEIEELGGPTAQ
>NZ_CP017704|3190835:3199965|3197903_3198299_-|WP_063234886.1|DBSCAN-SWA
MKHLPTSILTDILTEKIKRNSSEQYGNFVSSLNSLTEKQKTMEDLKQFDHHFDKFLPQLDLMISTQNHEAIMNMKATLLDLFANDLTFKSIYLLSIALSNKKELTHLNQFMYPVTFWAPVIKSNEMLKNAG
>NZ_CP017704|3190835:3199965|3194883_3196077_+|WP_063234884.1|DBSCAN-SWA
MMSKKRLFTSESVTEGHPDKICDQISDSILDAILAKDANARVACETSVTTGLVLVAGEITTSAYVDIPRIVRDTIKGIGYTRAKYGFDAETCAVLSSIDEQSADIAAGVDKALEAREGNMSEEEIDAIGAGDQGLMFGFACNETEELMPLPISLAHKLSFRLAQVRKDETLPYLRPDGKTQVTVEYDENNLPVRVDTIVISTQHDAEITLEQIQADLKEHVIKAVVPAELIDAETKYFINPTGRFVIGGPQGDAGLTGRKIIVDTYGGYARHGGGAFSGKDATKVDRSAAYAARYVAKNIVAAGLADKAEVQLAYAIGVAEPVSISIDTFGTGTVSEEVLVDLVRANFDLRPAGIIKMLDLRRPIYKQTAAYGHFGRTDVDLPWERTDKAETLKAQA
>NZ_CP017704|3190835:3199965|3199005_3199965_-|WP_063234888.1|DBSCAN-SWA
MNQANPFIYATDNKRYHTWNYHLREHFGHKVFKVALDGGFDCPNRDGTVAHGGCTFCSASGSGDFAGSRVEPLDVQFKKISERMHHKWKDGKYMAYFQAFTNTHAPVAELREKYESVLTQEGVVGLSIATRPDCLPEDVVEYLAELNERTYLWVELGLQTVHEKTATMINRAHDFDCYKEGVDKLRKHGIRVCSHIINGLPQEDYGMMMETAREVAKLDVQGIKIHLLHLLKGTPMVKQYEKGLLEFLDRDDYVSLVCDQLEIIPPEMIVHRITGDGPIDLMIGPMWSVNKWDVLNAIDAELKRRNSWQGKNHHMEVQS
>NZ_CP017704|3190835:3199965|3197029_3197833_+|WP_063234885.1|DBSCAN-SWA
MWKWETEGDAKGVIVIIHGAMEHHGRYKWVTQMWLSAGYHVVMGDLPGQGMTTRAYRGHIDSFDEYLDEVKSWIEEAYEYSLPVFLLGHSMGGLISIRLLQEEEWDIAGVILSSPCLGLVTKPRKFLTTISHGLNFVMPMFRVDSGLTPEMATRSAEVRESDRNDTLYITKVSIRWYRELAQAMKDAFEEIPEFQDVPLLVMQGGDDRIVNKKAVREWFNYNLASEKQYKEWPKLYHEIFNEPERDDVFQYALSFVENRLKILGYVV
>NZ_CP017704|3190835:3199965|3198436_3199009_-|WP_063234887.1|DBSCAN-SWA
MKLDRILPFARILLEKAVHPGDITIDGTMGNGFDTVFLAGLTGVDGHVYSFDIQEEAIQTTTAKLNAENLQERCTLIHDGHEHLSKYIRNEHSGKITGAIFNLGYLPGGDKSIITQADTTISAIEQLFELLAPEGIIILVIYHGHPGGSAERDALMDYVQNFPQQKAHILKYGFINQANNPPFIVAIEKR
>NZ_CP017704|3190835:3199965|3190835_3192137_+|WP_063234882.1|DBSCAN-SWA
MKLCTIGLGYIGLPTSLMFAKHGVDVVGVDIHPEIISNLNSGRLHIEEPGLDEVLEEVITSNKFRAALSPEHADVFIIAVPTPNKKDMHQSCDLTHVMDATSNILPFIKKGNVIIIESTIAPRSMDDHIRPMIERTGLTIGKDIFLVHCPERVLPGRILEELVHNNRIVGGITETCSYKGSLVYKTFVQGEIIQTDAKTAEMSKLMENTFRDVNIALANELTKVCFELDINVLDVISMANKHPRVNIHQPGPGVGGHCLAVDPYFVVAKSPEYAKIIKLARDTNVSMPYYIVNCVRMMLEGIRKPKVAVFGLAYKGNVDDIRESPAIDVVNILMGMENMDVALHDPHVQSGKMPVVSVEDAVNDADLILVLTDHDEFKQMDYDKLSNLMSNKLILDTRNCIDATKTDVPVANLGNIYQYKTMSMKKARNKAII
>NZ_CP017704|3190835:3199965|3196300_3196819_-|WP_063234974.1|DBSCAN-SWA
MIYPYKGKEPEIAESAYIAENAVVTGDVKIGDETSIWFNSVIRGDVSPTIIGKKVSIQDNSVLHQSPNNPLIIEDEVTIGHQVILHSCKIRKGALIGMGSIVLDEAEIGEGAFIGAGSLVPQGKVIPPNMLAFGRPAKVIREINEEDRQDMERIVREYAEKGQYYKTAERIK

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_063234882.1|3190835_3192137_+	nucleotide sugar dehydrogenase	A0A127AXI2	Bacillus_phage	3.8e-26	24.1
WP_063234883.1|3192537_3194127_-	phosphoenolpyruvate carboxykinase (ATP)	A0A2H4PQN1	Staphylococcus_phage	2.7e-191	63.1
WP_063234884.1|3194883_3196077_+	methionine adenosyltransferase	A0A2H4PQS6	Staphylococcus_phage	6.4e-161	74.1
WP_063234974.1|3196300_3196819_-	gamma carbonic anhydrase family protein	NA	NA	NA	NA
WP_063234885.1|3197029_3197833_+	alpha/beta hydrolase	A0A220T682	Eptesipox_virus	8.4e-08	22.6
WP_063234886.1|3197903_3198299_-	hypothetical protein	NA	NA	NA	NA
WP_063234887.1|3198436_3199009_-	16S rRNA (cytosine(1402)-N(4))-methyltransferase	A0A2H4PQV0	Staphylococcus_phage	9.2e-49	51.9
WP_063234888.1|3199005_3199965_-	TIGR01212 family radical SAM protein	A0A2H4PQV5	Staphylococcus_phage	2.1e-58	74.5