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_CP047310	Stenotrophomonas maltophilia strain CPBW01 chromosome, complete genome	3 crisprs	csa3,DEDDh,WYL,cas3,Cas9_archaeal,DinG	0	0	2	0

1. NZ_CP047310

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP047310_1

• CRISPR_ID: NZ_CP047310_1
• CRISPR_location: 335883-335978
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP047310_1

Consensus_repeat	Method
TTGGTAGGTGTCGACCTTGGTCGACACA	CRISPRCasFinder

spacers of NZ_CP047310_1

>1.1|335911|40|NZ_CP047310|CRISPRCasFinder
GTAGATCCACGCCATGCGTGGATGTTCTTCCGAATTCGCT

CRISPR arrays and Neighbor proteins around NZ_CP047310_1

CRISPR arrays

The CRISPR arrays of NZ_CP047310_1

>merge|NZ_CP047310|1|335883-335978|CRISPRCasFinder
TTGGTAGGTGTCGACCTTGGTCGACACAGTAGATCCACGCCATGCGTGGATGTTCTTCCGAATTCGCTTTGGTGGGTGTCGACCTTGGTCGACACA

>NZ_CP047310|1|1|335883-335978|CRISPRCasFinder
TTGGTAGGTGTCGACCTTGGTCGACACA	GTAGATCCACGCCATGCGTGGATGTTCTTCCGAATTCGCT
TTGGTGGGTGTCGACCTTGGTCGACACA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP047310.1|WP_159359680.1|322959_324864_+|hypothetical-protein	unknown	unknown	gnl|CDD|284995
NZ_CP047310.1|WP_053442400.1|340034_342092_-|potassium-transporting-ATPase-subunit-KdpB	unknown	unknown	gnl|CDD|234905
NZ_CP047310.1|WP_159359683.1|331520_332783_+|bifunctional-phosphopantothenoylcysteine-decarboxylase/phosphopantothenate--cysteine-ligase-CoaBC	unknown	unknown	gnl|CDD|235513
NZ_CP047310.1|WP_159359686.1|344091_344754_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP047310.1|WP_005420469.1|345595_346396_+|exodeoxyribonuclease-III	unknown	unknown	gnl|CDD|197336
NZ_CP047310.1|WP_049412124.1|333265_335611_+|phosphomannomutase/phosphoglucomutase	unknown	unknown	gnl|CDD|100091
NZ_CP047310.1|WP_159359685.1|342102_343812_-|potassium-transporting-ATPase-subunit-KdpA	unknown	unknown	gnl|CDD|235494
NZ_CP047310.1|WP_049480356.1|339387_340038_-|potassium-transporting-ATPase-subunit-KdpC	unknown	unknown	gnl|CDD|376890
NZ_CP047310.1|WP_010486900.1|328087_329776_-|arginine--tRNA-ligase	unknown	unknown	gnl|CDD|234964
NZ_CP047310.1|WP_029550913.1|329890_330595_-|JAB-domain-containing-protein	unknown	unknown	gnl|CDD|178801
NZ_CP047310.1|WP_159359687.1|346392_347766_+|MFS-transporter	unknown	unknown	gnl|CDD|341039
NZ_CP047310.1|WP_014645675.1|344773_345433_-|orotate-phosphoribosyltransferase	unknown	unknown	gnl|CDD|234771
NZ_CP047310.1|WP_159359684.1|336675_339336_-|DUF4118-domain-containing-protein	unknown	unknown	gnl|CDD|225115
NZ_CP047310.1|WP_159359682.1|325092_326355_-|conjugal-transfer-protein-TrbI	unknown	unknown	gnl|CDD|225499
NZ_CP047310.1|WP_010486901.1|327163_328066_-|SPOR-domain-containing-protein	unknown	unknown	gnl|CDD|225629
NZ_CP047310.1|WP_021204751.1|332779_333253_+|dUTP-diphosphatase	unknown	unknown	gnl|CDD|234802
NZ_CP047310.1|WP_010486889.1|335981_336695_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_CP047310.1|WP_019338987.1|330665_331292_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225107
NZ_CP047310.1|WP_159359681.1|324814_325096_-|DUF2274-domain-containing-protein	unknown	unknown	gnl|CDD|370791
NZ_CP047310.1|WP_005407770.1|343824_343917_-|potassium-transporting-ATPase-subunit-F	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP047310.1|WP_159359680.1|322959_324864_+|hypothetical-protein	gnl|CDD|284995	pfam07693, KAP_NTPase, KAP family P-loop domain. The KAP (after Kidins220/ARMS and PifA) family of predicted NTPases are sporadically distributed across a wide phylogenetic range in bacteria and in animals. Many of the prokaryotic KAP NTPases are encoded in plasmids and tend to undergo disruption to form pseudogenes. A unique feature of all eukaryotic and certain bacterial KAP NTPases is the presence of two or four transmembrane helices inserted into the P-loop NTPase domain. These transmembrane helices anchor KAP NTPases in the membrane such that the P-loop domain is located on the intracellular side.	1.7018e-13
NZ_CP047310.1|WP_053442400.1|340034_342092_-|potassium-transporting-ATPase-subunit-KdpB	gnl|CDD|234905	PRK01122, PRK01122, potassium-transporting ATPase subunit KdpB.	0
NZ_CP047310.1|WP_159359683.1|331520_332783_+|bifunctional-phosphopantothenoylcysteine-decarboxylase/phosphopantothenate--cysteine-ligase-CoaBC	gnl|CDD|235513	PRK05579, PRK05579, bifunctional phosphopantothenoylcysteine decarboxylase/phosphopantothenate synthase; Validated.	0
NZ_CP047310.1|WP_005420469.1|345595_346396_+|exodeoxyribonuclease-III	gnl|CDD|197336	cd10281, Nape_like_AP-endo, Neisseria meningitides Nape-like subfamily of the ExoIII family purinic/apyrimidinic (AP) endonucleases. This subfamily includes Neisseria meningitides Nape and related proteins. These are Escherichia coli exonuclease III (ExoIII)-like AP endonucleases and belong to the large EEP (exonuclease/endonuclease/phosphatase) superfamily that contains functionally diverse enzymes that share a common catalytic mechanism of cleaving phosphodiester bonds. AP endonucleases participate in the DNA base excision repair (BER) pathway. AP sites are one of the most common lesions in cellular DNA. During BER the damaged DNA is first recognized by DNA glycosylase. AP endonucleases then catalyze the hydrolytic cleavage of the phosphodiester bond 5' to the AP site, and this is followed by the coordinated actions of DNA polymerase, deoxyribose phosphatase, and DNA ligase. If left unrepaired, AP sites block DNA replication, and have both mutagenic and cytotoxic effects. AP endonucleases can carry out a variety of excision and incision reactions on DNA, including 3'-5' exonuclease, 3'-deoxyribose phosphodiesterase, 3'-phosphatase, and occasionally, nonspecific DNase activities. Different AP endonuclease enzymes catalyze the different reactions with different efficiences. Many organisms have two AP endonucleases, usually one is the dominant AP endonuclease, the other has weak AP endonuclease activity; for example, Neisseria meningitides Nape and NExo. Nape, found in this subfamily, is the dominant AP endonuclease. It exhibits strong AP endonuclease activity, and also exhibits 3'-5'exonuclease and 3'-deoxyribose phosphodiesterase activities.	3.94565e-146
NZ_CP047310.1|WP_049412124.1|333265_335611_+|phosphomannomutase/phosphoglucomutase	gnl|CDD|100091	cd03089, PMM_PGM, The phosphomannomutase/phosphoglucomutase (PMM/PGM) bifunctional enzyme catalyzes the reversible conversion of 1-phospho to 6-phospho-sugars (e.g. between mannose-1-phosphate and mannose-6-phosphate or glucose-1-phosphate and glucose-6-phosphate) via a bisphosphorylated sugar intermediate. The reaction involves two phosphoryl transfers, with an intervening 180 degree reorientation of the reaction intermediate during catalysis. Reorientation of the intermediate occurs without dissociation from the active site of the enzyme and is thus, a simple example of processivity, as defined by multiple rounds of catalysis without release of substrate. Glucose-6-phosphate and glucose-1-phosphate are known to be utilized for energy metabolism and cell surface construction, respectively. PMM/PGM belongs to the alpha-D-phosphohexomutase superfamily which includes several related enzymes that catalyze a reversible intramolecular phosphoryl transfer on their sugar substrates. Other members of this superfamily include phosphoglucosamine mutase (PNGM), phosphoacetylglucosamine mutase (PAGM), the bacterial phosphomannomutase ManB, the bacterial phosphoglucosamine mutase GlmM, and the phosphoglucomutases (PGM1 and PGM2). Each of these enzymes has four domains with a centrally located active site formed by four loops, one from each domain. All four domains are included in this alignment model.	0
NZ_CP047310.1|WP_159359685.1|342102_343812_-|potassium-transporting-ATPase-subunit-KdpA	gnl|CDD|235494	PRK05482, PRK05482, potassium-transporting ATPase subunit A; Provisional.	0
NZ_CP047310.1|WP_049480356.1|339387_340038_-|potassium-transporting-ATPase-subunit-KdpC	gnl|CDD|376890	pfam02669, KdpC, K+-transporting ATPase, c chain. This family consists of K+-transporting ATPase, c chain, KdpC. KdpC forms strong interactions with the KdpA subunit, serving to assemble and stabilize the Kdp complex. It has been suggested that KdpC could be one of the connecting links between the energy providing subunit KdpB and the K+-transporting subunit KdpA. The K+ transport system actively transports K+ ions via ATP hydrolysis.	8.49875e-85
NZ_CP047310.1|WP_010486900.1|328087_329776_-|arginine--tRNA-ligase	gnl|CDD|234964	PRK01611, argS, arginyl-tRNA synthetase; Reviewed.	0
NZ_CP047310.1|WP_029550913.1|329890_330595_-|JAB-domain-containing-protein	gnl|CDD|178801	PRK00024, PRK00024, DNA repair protein RadC.	4.47597e-120
NZ_CP047310.1|WP_159359687.1|346392_347766_+|MFS-transporter	gnl|CDD|341039	cd17486, MFS_AmpG_like, AmpG and similar transporters of the Major Facilitator Superfamily. AmpG acts as an inner membrane permease in the beta-lactamase induction system and in peptidoglycan recycling. It transports meuropeptide from the periplasm into the cytosol in gram-negative bacteria, which is essential for the induction of the ampC encoding beta-lactamase. The AmpG family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	3.79764e-106
NZ_CP047310.1|WP_014645675.1|344773_345433_-|orotate-phosphoribosyltransferase	gnl|CDD|234771	PRK00455, pyrE, orotate phosphoribosyltransferase; Validated.	6.34267e-82
NZ_CP047310.1|WP_159359684.1|336675_339336_-|DUF4118-domain-containing-protein	gnl|CDD|225115	COG2205, KdpD, Osmosensitive K+ channel histidine kinase [Signal transduction mechanisms].	0
NZ_CP047310.1|WP_159359682.1|325092_326355_-|conjugal-transfer-protein-TrbI	gnl|CDD|225499	COG2948, VirB10, Type IV secretory pathway, VirB10 components [Intracellular trafficking and secretion].	2.20559e-76
NZ_CP047310.1|WP_010486901.1|327163_328066_-|SPOR-domain-containing-protein	gnl|CDD|225629	COG3087, FtsN, Cell division protein [Cell division and chromosome partitioning].	3.81664e-18
NZ_CP047310.1|WP_021204751.1|332779_333253_+|dUTP-diphosphatase	gnl|CDD|234802	PRK00601, dut, dUTP diphosphatase.	1.05129e-89
NZ_CP047310.1|WP_010486889.1|335981_336695_-|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	5.89423e-73
NZ_CP047310.1|WP_019338987.1|330665_331292_-|response-regulator-transcription-factor	gnl|CDD|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	7.57719e-49
NZ_CP047310.1|WP_159359681.1|324814_325096_-|DUF2274-domain-containing-protein	gnl|CDD|370791	pfam10038, DUF2274, Protein of unknown function (DUF2274). Members of this family of hypothetical bacterial proteins have no known function.	5.93741e-23

Protein sequences

>NZ_CP047310.1|WP_049412124.1|333265_335611_+|phosphomannomutase/phosphoglucomutase
MSGIGEGQRGRSLGRSAPLLGVLLVLLAGWFGWSAVQQWRQEANGQALEAARDQAVQGLQEAAAGQLKQLQQQLKNERVQQALQAGDAAAAALAVRESWTGVEHAEVLTADLANAYADPATFGYARLALLEAALAETGPSLRVVRDGGGNRLGLAAPVPLGSLGPAVLYVRQPLLRLTSPLDQVSAPSAGFLGLRQGAHDLVAQGDASLAESAEALARPIPGTPLRLVAAVPNVEPGPLGLGSLASAIVALLLAFIAVLLVVGRGRLPKTLPLPRRAAVAEADHGPTLSESLQMAPPPVAEASTTESAPPPPPPVPAEELAAGIFRAYDIRGVVGSQLTPKTAALIGQAIGTVALEQGLREVVIGRDGRLSGPELAAGLAEGLRRAGCAVIDIGLAPTPVVYYAAFHLRTGTCVAVTGSHNPPEYNGFKVVIGGETLSGDAITDLYQRIIEGRLVQAAEPGDYQQRDVSADYIQRIADDVQLDRPLKVVADAGNGVAGALAPQLLEAIGAEVIPLYCDVDGTFPNHHPDPSEPANLEDLVQTVKRFGADLGVAFDGDGDRLGVVTGEGRIIYADRLLMLFAADVLMRNPGAMVIYDVKCTGKLSDHVLRNGGSPLMWKTGHSLMKAKMRETDAELAGEMSGHFFFKERWFGFDDGLYAAARLLEILAQREETPDEVLAELPEMVATPELKVPVADGTPHALVAMLVAAAQSPDNPYVGGRLSTIDGLRVDFPDGWGLVRASNTTPVLVLRFEGNDEAALERIQALFRSQLQPVLGETPLGF
>NZ_CP047310.1|WP_021204751.1|332779_333253_+|dUTP-diphosphatase
MTQAFTSQPLQVKLLDPRFGDSWPLPAYATEASAGMDLRAALDTALTLQPGDTALVPSGLAIHIADPNLCAVILPRSGLGHRHGIVLGNGTGLIDADYQGPLLISVWNRGREAFTIEPGDRIAQLVVVPIARVSLQVVDTFTDSVRGTGGFGHTGVR
>NZ_CP047310.1|WP_159359683.1|331520_332783_+|bifunctional-phosphopantothenoylcysteine-decarboxylase/phosphopantothenate--cysteine-ligase-CoaBC
MADSPNASPAPARALEGQKLLLCVGGGIAAYKALELVRRLRDAGAQVQVAMTAGAQQFVTPLSFQALSGQPTRTTLWDSAAEQAMGHIELARWADRIVVAPGTADLLARLAQGHADDLVSTLCLASTAPLTICPAMNHRMWLHPATQANIALLRQRGAQVIGPVDGPLAEGESGPGRLAEPGDIVAALAANGSATATVAAPETRALQGLRLLISAGPTYEDIDPVRYVGNRSSGKMGFALAAAAATMGAQVVLVSGPVQLPTPPGVQRVDVRSAAQMRDAVLKSLPADIYIGAAAVSDYTPRQVAAQKLKKTADSQSLVIELVRTPDILAEVAAQTQSLKLVVGFAAETHDVEKYARGKLVDKRLDLVIANQVGISGGGFESDNNAATAFWQDGEQVFPATSKRELAEQLLALIARRLQA
>NZ_CP047310.1|WP_019338987.1|330665_331292_-|response-regulator-transcription-factor
MHPRIIIADDHPVVLHGIRVVLQTHLMDIVGSARDGAQLLELVDQHDCDAVLTDLSMPGAGPDGPELIDALRMRRPGLPVVVLTGARHPGLLDGLLREGISGLVDKCADFAELPQALNAAMAGQVFVSQQLRHHLQARDLLFPREPAPLSAREQEVLELLAAGLNVNQVAERCGRSPKTISRQKAEAKRKLGLQNNQELFDYLQTRRD
>NZ_CP047310.1|WP_029550913.1|329890_330595_-|JAB-domain-containing-protein
MPIHDWPEQERPREKLIARGPTSLSDAELLALFLGSGFGGRDAVQTARDLLQAHGPLRVLLDRPARELARLPGLGPARSCTLVAGLELAHRYLAAELEHGEAVGNNPAAVGRYLQHRLRGQAREIFMALFLDNRHRLIACEELFHGTINAAPVYPREVVRRALLHNAAAVILSHNHPSGDPEPSSADTRITDELQQALAMVDVRLLDHFVVGEGRPVSFAERGLLSAPQPRLFG
>NZ_CP047310.1|WP_010486900.1|328087_329776_-|arginine--tRNA-ligase
MKNLLRALISQGIEALRANGTLPADSLPPDFVVERPKTRDHGDFATNAAMLLAKAARSNPRALAQALVEALPRSEDVSKVEIAGPGFINFHLAPAAYQREAASVIKEAHDYGRNLSGNGRTVGVEYVSANPTGPLHVGHGRAAAIGDCVARVLDANGWNAKREFYYNDAGVQIENLALSTQARIKGIAPDQDGWPEGGYRGEYIADVARAYMAGASVDLEGSTVVGAKDPDDMQAIRRFAVAYLRNEQNLDLAAFGVDFDIYFLESSLYADGKVAEAVAKLQASGHTYEEGGALWLRSTDFGDDKDRVMRKSDGTFTYFVPDVAYHLSKWQRGYERAITELGADHHGSLARVRAGLQAMEVGIPQGWPEYVLHQMVTVMRGGEEVKLSKRAGSYFTLRDLIEEAGRDATRWFLIARKPDSQLTFDIDLARQQSNDNPVFYVQYAHARVCSLLRQAQEKGLVYEQGNGLANLGRLADDASLLLMNEISRYPEVVEAAGVALEPHLVAQYLRELAHAFHTWYHGTPVLVDDAADRNAKLTLACAARQVLANGLELLGVSAPEKM
>NZ_CP047310.1|WP_010486901.1|327163_328066_-|SPOR-domain-containing-protein
MAARRGKNQARRNSSSQGTPGWVWLVAGVAIAAVVFLAAPNLFKGEGDGFLRAGPQPNPNAQPAPVADADSDVGAQPAAQPATPKPAEPEKPAATQYDFYTLLPGKEVEMSDAELAASARAEDQRRAKAEAQRAQAALEGKPVPAAAAAPAPTATASVASTAPVTATSRPLPAPLSERPAAATPPASTPTASTSAAAATPAARAETPPTAASTPAAAAPAAADNARYILQAGAFGASGDAEATKAKLAMMGLAARVESAQINGKTVYRVRMGPYGSAGELSEAKQKLDGTGLQAMAIKAQ
>NZ_CP047310.1|WP_159359682.1|325092_326355_-|conjugal-transfer-protein-TrbI
MRPEDSAPAAGKVAPEAMTLRAPPRPVTRLNRRTLMLLASGLAVAVLVATMWGLRSPSRESSQALELYNVDRVAKPEGLDGLPADYSKLPPKAPELGPPLPGDLGPAILASQQPVTATYQAPGEDPEEARRKEAESAAGSSVFFRSGGQGAAAAPATAAAAAPSAESSLTGFDPLAAGPHSAAPQPHDPTAVQNRQDEKEAFLRKGGAAQTRNSGDLQLAASPYQVMAGTVIAAALVTGVKSNVPGDVIGTVTEPVYDTATGKFVLIPQGSRVLGKYSSQVSYGQTRVQVVWHRIILPDTSSLNLDNLVGTDPAGYAGLQDEVDGHWGRLFASAALTTILGVGAELAAPENRQDGNRVVIAGRDSAQDGVNQLGQELTRRSLNVQPTLSARPGLPVRLIVSRDLVLRPYQPMFFVRGSLP
>NZ_CP047310.1|WP_159359681.1|324814_325096_-|DUF2274-domain-containing-protein
MSTGRKLRLGPLPKLESTRVTFVCPAALKAELDRYAAMHSQAYGESVDAAALIPLMLEAFMDGDRGFRRGKHASPVGPKLLLRNRALHQDRRR
>NZ_CP047310.1|WP_159359680.1|322959_324864_+|hypothetical-protein
MISRIWKKFMPSKAEERAPGASSETKKNSGNEMADRNVHVKEYLRYYLSLSTSPGFAVLLDGPWGIGKTFVIKTFLDTLDKETTPYIYVSLYGIQSVDDIDDAILQGMYPVLANKGVELGGRALKSIGKYFNVELDLKAKDFLKKSKADVYVFDDLERCEMPINAVMGYINVFVEHEGRKVILIANENEIEDQPKYKRIREKLVGRTFEVQSSFEEALDGFVASAKDEAAKKFLSSASSTISEVYHQSEMNNLRVLQQTILDFERLYIVLEERHRKNDEAMKALLALLFALSFEVKAGRLAADDMKNRQTHLLSSYIQNKKDDYVPPKIVAVNNRYPLARIDADLLSDDTLVDLIVRGIIDRRKLRDELDSSSFFFTAEKEPAWRTVWNSHERTEEEFNVALAEMTRAFAAHEYTVLGEIRHVFGIQLRLSGIGVTTASRAQVVADAKSYVDYLYDHKLLEPIEPHRDSFDVNFDSYAGLGYMEASSAEFRELSEYLNQKRHAAAVDRRPAIAKDLLTLMVEDPSQFLRRICLTNHEDNEFYDIPVLASLDVRKFVDAFLGLHPAKQKTVILALKLRYQHRMLDRDLEDERPWATEVRSQILAASGAMSPISKDRIQRLIAYGLDEALDSARGA
>NZ_CP047310.1|WP_010486889.1|335981_336695_-|response-regulator-transcription-factor
MSPTPIEASAPAARVLVIDDETQIRRFLDISLRAQGYQVRQAATGQEGLQLAASEDMDLVILDIGLPDMEGHEVLEQLRQWSQVPVIMLTVRAGEAEKVRALDTGANDYVTKPFGTQELMARVRALLRTRSVPSDGTPPVFDDGHLHVDLVRREVALDGEPVALTRKEYALLSLLLRNAGRVVTQPQILQEIWGPTHQHDTHYLRILVGKLRHKLGDSALDSRYLFTEPGVGLRFKG
>NZ_CP047310.1|WP_159359684.1|336675_339336_-|DUF4118-domain-containing-protein
MTDARTRQADALVEGLQREAGGKLTVFLGAAPGVGKTYTMLTRAQEQLRRGVDLVVGLVETHGRADTQALLEGLPQLSLKAVAYHGHTLQEMDLDAVLARHPALVLVDELAHRNAPGSRHERRWQDVMELLDAGIDVWTTVNIQHLESLNDVVMRITGVRVSETVPDGVLDRLHDIVLVDLPPRELIARLQQGKVYVPEQAAQALQAFFSPANLTALRELAMQEAADRVDSSLRETRAARGEGNLPLRRGVLVAIDGGGQSEYLVRVARRIAERRDAPWTVVTVQGRRQDEATRREIDAAFALARRLGGDAELLHGSSIADALLDHAAHNGVSTLVLGRTRERPLARMFNRTLTQQLIQRGAHYEITIISTPQARARSRRESLLPPMRGISHEPAQALIATALACAVAWLAEHWVGMADLSMVFIVAVVLVAARTRASVAVMAAILCFLAYNFLFIAPRFTFAISARQGVITVFLFLAAALVAGRLASRLRMQVIALRAANRHARARQQLGRQLASAAGNGEVAQAGRHALEQAMDVPAWLRIGADTATGGRSQPGDTDLAAADWALRHGQPSGRFTDTLAGAQWWFLPLLDGEDRAIGVAGLYLPGAQARLLPEQRQLAEAMVDDIAQAALRTRLVAELEQAHVSNETERLRSALLSSVSHDLRSPLAAMIGSADSLASYGTAMDTADRRALLDTILVEGERLDRYIQNLLDMTRLGHEGLKINRDWIGVDELIGSAARRLQRYQPKVRLELDIPSTLAPIWVHPALVEQAVFNVMENAAKFSPPDAAVQVQARELDGQLRIDVIDAGPGIPDDERARIFDMFYSVERGDRGRHGTGLGLTICQGMIGAHGGSVQALPGRDGRGTLIRITLPLLKPASHDEPDPD
>NZ_CP047310.1|WP_049480356.1|339387_340038_-|potassium-transporting-ATPase-subunit-KdpC
MNRTVSTSSSLPREQKAEARVASLQDGASWRPAIGLGLATLLLAGAVYAGIATGFAGLAFPGQAEGSLLRDDSGQVRGSVWLAQPFTGDGYFQARPSAANYDPMAAAGSNMARSNPALAERVAASTAAVAAREGVAPAQVPADLVTQSGGGLDPQLSPAAAQLQVARVARARGLPVARVQALVQAHTEGRQWGLFGQPRVNVVTLNFALDHAAKAP
>NZ_CP047310.1|WP_053442400.1|340034_342092_-|potassium-transporting-ATPase-subunit-KdpB
MSTHASSTRSSLAPRPALLDGAGLRRALVDAVRKLSPMHLVRSPVMAVVMAGTIVAAIVTLTGNAPLGFGLAVTAILLVTVLFGNFAEAVAEARGRGQAASLRRARQDLVARRLAAPQPGAAETQVPAAELRPGDHVIVSAGELVPADGEIVQGLATINEAAVTGESAPVLREAGTDRSGVIGGTKVLSDQIIVRVTAEPGHSFLDRMIALVEGANRQKTPNEIALTLLLAAMTLTFLVVVATLPAIGASVGVKVDPLLLIALLVCLIPTTIGGLLPAIGIAGMNRALAANVLAKSGKAVEVAGDVDVLLLDKTGTITYGDRQASHFHPLAGIDASQLREAALLSSLADPTPEGKSIVRLAREQGCATAEPDHADYLAFTAQTRMSGVDLEHGRQIRKGAADAIRAHVQALGGNVPAELAGRVEQVARNGATPLVVAEGRHVLGVIELSDVVKHGMREKFAQLRAMGIRTVMITGDNPLTAAAIAAEAGVDDYIAEARPEDKLARIRQEQAGGRLVAMVGDGTNDAPALAQADIGLAMNSGTQAAKEAGNMVDLDSDPAKLLAVVEVGKQQLITRGALTTFSLANDVSKYFAILPALFAAAVPTMAALNVMQLSSPRNAVLAALIFNALVIPALIPLALRGVRFRPATATALLRRNMLVYGLGGVLLPFAAIKAIDLLLVLVFGA
>NZ_CP047310.1|WP_159359685.1|342102_343812_-|potassium-transporting-ATPase-subunit-KdpA
MTEMLVIIAASLLLAWPLGLYLARVMRGTPMKVDVLFHWIEKPLYRVFGVDPSRSMSWRGYVLAFVLSNVVVAVLTQAVFMTQAWLPLNPDQIPNMRWDTALHTMISFLTNTNQQHYSGQAQLSYLSQMTGITGLQVVTPMMGLALAVATLRALFSRAPQAAAATGSGDDRQVAVGNYYVDVVRLCVRFLLPLCLVWTLVLTSQGVPSTTAGGPQATPIDASAGMAGQKLPLGPVAAMVAAKQLGANGGGWYGPNSSFPLENPTPLSNALEIVGILLVPMAVIFMIGAFTGRRRFGALVFSCMLGMSLLSTGAMMWSEGHSASAATPLLMEGKEVRFGADGTALWAAVTTQVSNGSVNGMHDSLAPLSGGIAMVNMLVSAIWGGIGCGLQQFIVYLLLGVFLAGLMTGRTPEMFGRKLETPQVRLLALLVLLQPITLLVFTAITLAVPGLAGTSNPGFHGISQVFYEYVSAYANNGSGFEGLGDATLWWNLSCSLVLLLGRFPLLIIPLVVAAQLAAKRQAPESAGSLQIETPTFALTLVSVIVILTVLQFMPALVLGPIADHLSLGLH
>NZ_CP047310.1|WP_005407770.1|343824_343917_-|potassium-transporting-ATPase-subunit-F
MSPWLSLLCGVLVLVAAAYLLYVVLRPESF
>NZ_CP047310.1|WP_159359686.1|344091_344754_-|hypothetical-protein
MSRVPAVLFASLLLAVPFTVPAQPRGGDKTEKKLYCWNEGKERICSDSLPADAVNHAREEFNAKSGLRNAQVQRALTDEERAAASTVAAQQQLDLMAEQTRQRTEQAMLTTYGSEDDLRRVFAERQEVLDNNLKTAEYNVTSLRESLVALLSAAGDRELAGAKVADKQAGAIRQRHVQLQAQQRLQAGFLQQQQALKAEIESTLQRYRELKGVAPAAPAG
>NZ_CP047310.1|WP_014645675.1|344773_345433_-|orotate-phosphoribosyltransferase
MSDHRHRFLQLALTADALRFGQFTLKSGRLSPYFFNAGRFDSGSLLSQLGACYADAIDATGIKYDVVFGPAYKGIPLATAMACELAQRGRDLPLSFNRKEAKDHGEGGQLIGADMNGKRVLIVDDVITAGTAIREALGIIRAAGGTPAGIVVALDRQEIASEADRRSAAQSVAEEAGIPVIAVASLADLLDFASGNPELVGYRQPLEAYRAQYGVRSIR
>NZ_CP047310.1|WP_005420469.1|345595_346396_+|exodeoxyribonuclease-III
MRIISFNANGIRSAATKGFLDWFRAQDADVLCIQETKAQEDQLTDPMFRPDGHHCFYRDAITKKGYSGVAIYSKREPDQVITSLGWAPFDDEGRYIEARYGNLSVVSFYIPSGSSGDLRQGFKFEVMEWLRPILEEWARSGRDYVLCGDWNIVRSALDIKNWKSNQKNSGCLPEERDWLNALCADHGQATDVAAGRGWADAYRLLNPTGEDYTWWSNRGAARANNVGWRIDYQFITPGLRDKLRSCSIYRDERFSDHAPFTVDYDL
>NZ_CP047310.1|WP_159359687.1|346392_347766_+|MFS-transporter
MTEAAKPRRPWQQVLSNLSQRKVLAMLLLGFSSGLPIYLVGNTLGFWMRKEGIELSTIGFLSWVGLAYTMKFLWAPIVDKTDVPLFGRFGRRRGWMLLSQLVVVVGLVGMALVQPKGGQIQFLGIAWQHIVVFGVMAVIVAFASATQDIVIDAWRIESADNSEQLGLLTSSSALGYRTALLVTDALILIIAARVGWQVSYEIMAVLMALGVVAVVMAREPAREVAAVQAQATSLWTPRGLFDAVAGPFIAFVREHRSGAILILVAISVYRMADFVMGPMANPFYVDLGLDEDTVGAVRGSVGLVATFVGIAAAGLVSVRWGVLAALMVGAVLGPASNLAFAWLAYSGPDTTHFAVAMAIDNFASGFAGTALIAYMSSLTSIGYTATQYALLSSFYAMPGKALKGLSGWSVQTLAQGRTLLEGYALFFVGTALVAIPVVILCALLILQQRRRQAASST

Crispr_ID: NZ_CP047310_2

• CRISPR_ID: NZ_CP047310_2
• CRISPR_location: 426456-426547
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP047310_2

Consensus_repeat	Method
CCCCGGCCGCCGATGCCGCCGCC	CRISPRCasFinder

spacers of NZ_CP047310_2

>2.1|426479|46|NZ_CP047310|CRISPRCasFinder
CCGGCCGCCGATGCCGCCGCCCCGGCCACCACCGAGCAGGCCGCCA

CRISPR arrays and Neighbor proteins around NZ_CP047310_2

CRISPR arrays

The CRISPR arrays of NZ_CP047310_2

>merge|NZ_CP047310|2|426456-426547|CRISPRCasFinder
CCAAGCCGGCCGACACCGCTGCCCCGGCCGCCGATGCCGCCGCCCCGGCCACCACCGAGCAGGCCGCCACCCCGGCTGCCGATGCCGCCGCC

>NZ_CP047310|2|2|426456-426547|CRISPRCasFinder
CCAAGCCGGCCGACACCGCTGCC	CCGGCCGCCGATGCCGCCGCCCCGGCCACCACCGAGCAGGCCGCCA
CCCCGGCTGCCGATGCCGCCGCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP047310.1|WP_159360774.1|436878_437592_-|HNH-endonuclease	unknown	unknown	gnl|CDD|379157
NZ_CP047310.1|WP_010484192.1|425717_426308_+|malonic-semialdehyde-reductase	unknown	unknown	gnl|CDD|180040
NZ_CP047310.1|WP_159359707.1|429260_429821_-|PadR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224609
NZ_CP047310.1|WP_159359706.1|428402_429200_-|SIP-domain-containing-protein	unknown	unknown	gnl|CDD|99790
NZ_CP047310.1|WP_159359703.1|421667_422228_-|queuosine-precursor-transporter	unknown	unknown	gnl|CDD|224652
NZ_CP047310.1|WP_099551328.1|416827_418342_-|acetyl-CoA-hydrolase/transferase-family-protein	unknown	unknown	gnl|CDD|274588
NZ_CP047310.1|WP_159359711.1|435198_436806_+|ADP-ribosylglycohydrolase-family-protein	unknown	unknown	gnl|CDD|377122
NZ_CP047310.1|WP_010484201.1|415370_416732_+|VOC-family-protein	unknown	unknown	gnl|CDD|319958
NZ_CP047310.1|WP_159359705.1|427363_427765_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP047310.1|WP_100447494.1|422304_422817_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP047310.1|WP_159359704.1|423372_424224_-|DUF2145-domain-containing-protein	unknown	unknown	gnl|CDD|227071
NZ_CP047310.1|WP_159359708.1|430366_433054_+|pyruvate-dehydrogenase-(acetyl-transferring),-homodimeric-type	unknown	unknown	gnl|CDD|236500
NZ_CP047310.1|WP_057499938.1|438256_438625_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP047310.1|WP_010484193.1|424631_425591_-|nucleoside-diphosphate-sugar-epimerase	unknown	unknown	gnl|CDD|377637
NZ_CP047310.1|WP_159359710.1|434558_435209_+|DUF4433-domain-containing-protein	unknown	unknown	gnl|CDD|373093
NZ_CP047310.1|WP_159359709.1|433155_434562_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|223288
NZ_CP047310.1|WP_049443513.1|424272_424503_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP047310.1|WP_159359702.1|418729_421525_+|bifunctional-[glutamate--ammonia-ligase]-adenylyl-L-tyrosine-phosphorylase/[glutamate--ammonia-ligase]-adenylyltransferase	unknown	unknown	gnl|CDD|236836
NZ_CP047310.1|WP_100053258.1|422849_423410_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP047310.1|WP_159360775.1|439111_439333_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP047310.1|WP_159360774.1|436878_437592_-|HNH-endonuclease	gnl|CDD|379157	pfam13391, HNH_2, HNH endonuclease.	1.20466e-15
NZ_CP047310.1|WP_010484192.1|425717_426308_+|malonic-semialdehyde-reductase	gnl|CDD|180040	PRK05365, PRK05365, malonic semialdehyde reductase; Provisional.	1.96255e-127
NZ_CP047310.1|WP_159359707.1|429260_429821_-|PadR-family-transcriptional-regulator	gnl|CDD|224609	COG1695, COG1695, Predicted transcriptional regulators [Transcription].	1.16809e-17
NZ_CP047310.1|WP_159359706.1|428402_429200_-|SIP-domain-containing-protein	gnl|CDD|99790	cd06193, siderophore_interacting, Siderophore interacting proteins share the domain structure of the ferredoxin reductase like family. Siderophores are produced in various bacteria (and some plants) to extract iron from hosts. Binding constants are high, so iron can be pilfered from transferrin and lactoferrin for bacterial uptake, contributing to pathogen virulence. Ferredoxin reductase (FNR), an FAD and NAD(P) binding protein, was intially identified as a chloroplast reductase activity, catalyzing the electron transfer from reduced iron-sulfur protein ferredoxin to NADP+ as the final step in the electron transport mechanism of photosystem I. FNR transfers electrons from reduced ferredoxin to FAD (forming FADH2 via a semiquinone intermediate) and then transfers a hydride ion to convert NADP+ to NADPH. FNR has since been shown to utilize a variety of electron acceptors and donors and has a variety of physiological functions including nitrogen assimilation, dinitrogen fixation, steroid hydroxylation, fatty acid metabolism, oxygenase activity, and methane assimilation in a variety of organisms. FNR has an NAD(P)-binding sub-domain of the alpha/beta class and a discrete (usually N-terminal) flavin sub-domain which vary in orientation with respect to the NAD(P) binding domain. The N-terminal moeity may contain a flavin prosthetic group (as in flavoenzymes) or use flavin as a substrate. Because flavins such as FAD can exist in oxidized, semiquinone (one-electron reduced), or fully reduced hydroquinone forms, FNR can interact with one and two electron carriers. FNR has a strong preference for NADP(H) vs NAD(H).	8.97861e-89
NZ_CP047310.1|WP_159359703.1|421667_422228_-|queuosine-precursor-transporter	gnl|CDD|224652	COG1738, yhhQ, Uncharacterized member of the PurR regulon [General function prediction only].	2.32365e-32
NZ_CP047310.1|WP_099551328.1|416827_418342_-|acetyl-CoA-hydrolase/transferase-family-protein	gnl|CDD|274588	TIGR03458, Propionyl-CoA:succinate_CoA_transferase, succinate CoA transferase. This family of CoA transferases includes enzymes catalyzing at least two related but distinct activities. The E. coli YgfH protein has been characterized as a propionyl-CoA:succinate CoA transferase where it appears to be involved in a pathway for the decarboxylation of succinate to propionate. The Clostridium kluyveri CAT1 protein has been characterized as a acetyl-CoA:succinate CoA transferase and is believed to be involved in anaerobic succinate degradation. The propionate:succinate transferase activity has been reported in the propionic acid fermentation of propionibacterium species, where it is distinct from the coupled activities of distinct nucleotide-triphosphate dependent succinate and propionate/acetate CoA transferases (as inferred from activity in the absence of NTPs). The family represented by this model includes a member from Propionibacterium acnes KPA171202 which is likely to be responsible for this activity. A closely related clade not included in this family are the Ach1p proteins of fungi which are acetyl-CoA hydrolases. This name has been applied to many of the proteins represented by this model, possibly erroneously.	0
NZ_CP047310.1|WP_159359711.1|435198_436806_+|ADP-ribosylglycohydrolase-family-protein	gnl|CDD|377122	pfam03747, ADP_ribosyl_GH, ADP-ribosylglycohydrolase. This family includes enzymes that ADP-ribosylations, for example ADP-ribosylarginine hydrolase EC:3.2.2.19 cleaves ADP-ribose-L-arginine. The family also includes dinitrogenase reductase activating glycohydrolase. Most surprisingly the family also includes jellyfish crystallins, these proteins appear to have lost the presumed active site residues.	4.16666e-20
NZ_CP047310.1|WP_010484201.1|415370_416732_+|VOC-family-protein	gnl|CDD|319958	cd16348, VOC_YdcJ_like, uncharacterized metal-dependent enzyme similar to Shigella flexneri YdcJ. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	0
NZ_CP047310.1|WP_010484193.1|424631_425591_-|nucleoside-diphosphate-sugar-epimerase	gnl|CDD|377637	pfam06258, Mito_fiss_Elm1, Mitochondrial fission ELM1. In plants, this family is involved in mitochondrial fission. It binds to dynamin-related proteins and plays a role in their relocation from the cytosol to mitochondrial fission sites. Its function in bacteria is unknown.	1.28412e-92
NZ_CP047310.1|WP_159359704.1|423372_424224_-|DUF2145-domain-containing-protein	gnl|CDD|227071	COG4727, COG4727, Uncharacterized protein conserved in bacteria [Function unknown].	9.4644e-86
NZ_CP047310.1|WP_159359708.1|430366_433054_+|pyruvate-dehydrogenase-(acetyl-transferring),-homodimeric-type	gnl|CDD|236500	PRK09405, aceE, pyruvate dehydrogenase subunit E1; Reviewed.	0
NZ_CP047310.1|WP_159359710.1|434558_435209_+|DUF4433-domain-containing-protein	gnl|CDD|373093	pfam14487, DUF4433, Domain of unknown function (DUF4433). This family of proteins is found in bacteria, archaea and eukaryotes. Proteins in this family are typically between 201 and 230 amino acids in length. There is a single completely conserved residue E that may be functionally important. This family is distantly similar to pfam01885 suggesting these may be ADP-ribosylases.	3.20872e-17
NZ_CP047310.1|WP_159359709.1|433155_434562_+|AAA-family-ATPase	gnl|CDD|223288	COG0210, UvrD, Superfamily I DNA and RNA helicases [DNA replication, recombination, and repair].	9.0012e-11
NZ_CP047310.1|WP_159359702.1|418729_421525_+|bifunctional-[glutamate--ammonia-ligase]-adenylyl-L-tyrosine-phosphorylase/[glutamate--ammonia-ligase]-adenylyltransferase	gnl|CDD|236836	PRK11072, PRK11072, bifunctional [glutamate--ammonia ligase]-adenylyl-L-tyrosine phosphorylase/[glutamate--ammonia-ligase] adenylyltransferase.	0

Protein sequences

>NZ_CP047310.1|WP_010484192.1|425717_426308_+|malonic-semialdehyde-reductase
MSHALDAAALDQLFRTARTQNAFLDKPVPESLLKELYDLVKWGPTAANTTPARFVFVTSKEAKDKLAPALSEGNLAKTMAAPVTVIIGFDLDFHEKLPYLFPHTDAKAWFDGPQEGRHEAAIRNGSLQGAYLILAARALGLDAGPMSGFDPAKVDEAFFAGTSIKSNFLVNLGYGDSAGLFPRLPRLSFDEAARIA
>NZ_CP047310.1|WP_010484193.1|424631_425591_-|nucleoside-diphosphate-sugar-epimerase
MVKRSSAPWTVTDGRAGNVRQAVALASALRQGTHRPLVLQPRAPWRWLSPRRLPGDVNGYGEAFATLAADAPALAIGCGRQAAGALRVLRARGSQVVQILDPRINARHWDVVVVPEHDALRGSNVLTLLGSLNPVDDDWLAWGRAAFAGFSTLPGPRTALLVGGPTPLAPWDETSMVGVFRALADQIHSEGGSLLATTSRRTPPALAEILRATFADLPHVIWGDGGDGTNPYGGLLGWANRVVVSPDSVNLLSEACATRMPVMVALADTAQGRLARFQQQLRERGRLQAHWLDWQYDRIEPLRETARVAAEVKQRLALG
>NZ_CP047310.1|WP_049443513.1|424272_424503_-|hypothetical-protein
MRTLLLLPLALLAACSTAPTELDPISYQCQQQLDAYREQPALRDPKTGERPPLPIAPISDACDRELKRKGVDRPLR
>NZ_CP047310.1|WP_159359704.1|423372_424224_-|DUF2145-domain-containing-protein
MDRFSRLPRAALLIASLLATAPAWANSTECRERYPSVASQAAMLDVAWTTAERLDALPDVDVVVAARGGQDLSRYGLRHSHLAFLLREDDGRWRAMHLLNRCKTDSSQLYHEGLGNFVGESGGHIDLRIGVPAAPLRAALKAMLVSPSIQPKALHETRYNVVAYPFATDYQNSNQWVLEVLAAAMAQAEGAPAIVKREQAQQWLRQQKYQPSVLHIGLGKRVGARLFVANATTTDHPAGERISGNYSVVTVESVFDFLHQRSQLQQELVIPHVPVAGAAAATP
>NZ_CP047310.1|WP_100053258.1|422849_423410_-|hypothetical-protein
MYRWPVLPPPRPESSKENDMRTLPAFLMPMLIVASLAWSTAAHAERRIVIIHDPGPQGPSLEMSSQMVNSARAAAAKEAQDAADAGQPLARPQQIKLPQMQVSAIATTVDGRREVLLRDANDPQNTASMQYPRGIGDPAVQFTVGQTVNFEPTGNDQGWQLKDNQGRPLEYLPEATGPRDIFDTRR
>NZ_CP047310.1|WP_100447494.1|422304_422817_-|hypothetical-protein
MFRCLRVPATALLLSALLVPTVHAGAAPELNSSEASVLITSLIVVSVPLAASAGLSELSKAPFKASERNARAARTKAVPLPPMDVKKVETTAAGERQVQLQVPGKADQTATLRWPARVHEDQTAAFVVGQQVHFDPTEAGAGWTVKSAQGQALAYVPTAYAAGDVMSEAL
>NZ_CP047310.1|WP_159359703.1|421667_422228_-|queuosine-precursor-transporter
MSVRPAPVFAPLTARALVLAVLAMGAVVLLSNVLVQYPINDWLTWGAFSYPVAFLVSNLINRRFGPGPARRVAWIGFAVAVLLSIWVATPRIAIASCSAFIVAQLLDITVFDRLRRGSWWRAPMVATTCSATVDTTIFWSIAFAGSALPWVSWAAGDLAVKLAIGVCLLAPFRALLWKMAPLRATS
>NZ_CP047310.1|WP_159359702.1|418729_421525_+|bifunctional-[glutamate--ammonia-ligase]-adenylyl-L-tyrosine-phosphorylase/[glutamate--ammonia-ligase]-adenylyltransferase
MTLAPAELSAALQPVVDRALARLAQVLPEPVPAELLPLLTRLAVTSDFALDTLVRQPALLAQLAAPGCPPIPAPVLDPLQPSDWPAQIRRWRTAMSTRLIWRDLAGLDDVPQTLAGATALAEDCLRLALDALQQEFAQRHGVVRDGEGTPQQLVVFGLGKLGGGELNFSSDVDLVYAYPHGGESDGARALAAEEYFARLGQRLAKLLDETTVDGFSHRVDLRLRPFGSAGRVALSFAAMDQYFQREGRDWERYAWLKARAVAGDIAAGEAWLQTLRPFVYRRYLDFTALDGLREMKAAITAEVARRELHEDIKRGAGGIREIEFLCQALQLIRGGREPALRERRLLVALDALVAAGQIAPEDGSALREAYLFLRRLENRLQMLRDAQTHVLPSDALDRERIAVGLGYPDWDVLRAALAVQQARVSTEFAALLAPRKGQAAPDALANYWRSLPEGANAPLLAEAGFLDANGADQSLRDFAQGTGVKSLSDAARARLDRVLPALLHAATRSPQPDAALKRVLGLLQAVLRRTSYLALLDEQPSALARLVDVLARSALLAERLAAYPLLLDELLDVRVSGPMPDAAGMLAECQQVLAVEDPESALRWLNETRLALSFRMAMATLDGRQGAVDSTRQLAELAQAVVVTVLAMAEADMRAAHGEIPGGRFAIIGYGSLGGLELGFGSDLDLVFLHDNPAGVDASDGARPLEPGRWYARLAQKVMALLGAVTAAGRLYDIDVRLRPDGGKGSLVSSLASYTEYQRERAWTWEHQALVRARGVAGDASLLADFEQVRAQTLGRERDPATLYADVLKMRGRMRTELDRSDAARLDLKQGAGGVVDLEFLLQTGVLARSAQHAALLQPRDTPSLIDALAVVGFLPEDTAEALHGAHATLLDVGLACTLDRRPRLAPTTPAIEEACAAITAACRAAELPFG
>NZ_CP047310.1|WP_099551328.1|416827_418342_-|acetyl-CoA-hydrolase/transferase-family-protein
MSVDRIANARLRDRVVSAEAAAALIQPGETVAMSGFTGSGYPKAVPVELARRIEAVHAQGQPFQISLMTGASTAPELDGALAKADGIAMRMPFQSDPDARNRINEGKLDYIDIHLSHVAQHVWFGFYGEIDTAVIEVSAIREDGSLVPSTSVGNNKTWLDLAKKVIVEVNEWQPAGVDGMHDIYYGTALPPHRKPIPLVNANDRIGDTALRCDPDKIVAVVRTNGPDRNSPFSPIDATSEQIASHLIEFLQHEVKKGRLPPNLLPLQSGVGNIPNAVLAGLAKSGFRDLAAFTEVIQDGMLDLLRDGVLSYASCTGFALSPQANETFKENIDFYRERIIMRTQEISNHPELVRRLGCIGMNGMIEVDIYGNVNSTHVMGTRIMNGIGGSGDFARNGFLSAFLSPSTAKNGTISAIVPMASHVDHTEHDVSVIVTEQGLADLRGLTPRKRAQVLIDNCAHPDFRPQLQDYFDRASRESYGKHTPHLLPEALSWHQRWLDTGTMKG
>NZ_CP047310.1|WP_010484201.1|415370_416732_+|VOC-family-protein
MSASFVSPDVIRRLFAQAMSRMYRTEVPLYGTLVELVERINAQVLEQDPALAAQLQRNDERARLDEERHGAIRVGTVQELATLRRLFAVMGMYPVGYYDLSVAGVPVHSTAFRPLTGAALAQNPFRVFTSLLRLELIEDEALRAESAKILARRRIFTEGALALIDQAERDGGLAQADAERFVEQALETFRWHGDATVDLPTYHALHNAHRLVADVVSFRGPHINHLTPRTLDIDAAQAAMIEHGMAAKAVIEGPPRRACPILLRQTSFKALEEAVHFPDAEGGDAGTHTARFGEIEQRGLALTPKGRALYDQLLSQARDAGGEGSTGGDYGQRLQAVFASFPDDHDTLRQEGLGYYRYQLTDAGRAAPERVADLPAEVLVAAGLATADPIVYEDFLPVSAAGIFQSNLGGEEQRAYAAHANREAFEQALGVAVNDEFEIYERLQAESLAALRA
>NZ_CP047310.1|WP_159359705.1|427363_427765_-|hypothetical-protein
MAKLTLASVDALRTRFADDAACDAALAAFADTKALRTPLRELVEAQHRYLQAEFEVAQVADVLRRDQKYAPVGRPSVHIVQLRKQQAATKQAALIARQVVAQAAQTFVRVSGMTVKAKQSPSETCVAWLGALR
>NZ_CP047310.1|WP_159359706.1|428402_429200_-|SIP-domain-containing-protein
MTEHNNTRLRLDVRFRELTVMRTEEVTPHMRRIVLGGDALAGFDSPGADDHIKLFFPNAAGEMVLPVLTAEGRSYPDGKEPSPARDYTPRWWDHETGELAIDFVLHDQGIAGPWAESAQPGDTLVIGGPRGSFVVADTYDAYVLIGDETALPAIARWLDVLPEDAEVQAFIEVSDEAERQDLPQYENVRIHWLERNGFPAATSTLLEDMLTDFEAPEGDVFYWIATESRRARMMRKFIEGHLGVPRDWIRSTGYWKAHPDETDGD
>NZ_CP047310.1|WP_159359707.1|429260_429821_-|PadR-family-transcriptional-regulator
MSRSPSPRARSTDSAVPRRNGQPRVLSRGDLRLLVLALIGEQPRHGYELMQLISNQFMQAYTPSAGTMYPLLASFEQAGWIEAEEVDGKRIFRITAAGEFELKVQRTQVRLAQRRAFDRAREITKASLPAPLACALREFKRALVHHHGRWAEGEADEVAALLTRASALLNGTAGNERPPISMTQPD
>NZ_CP047310.1|WP_159359708.1|430366_433054_+|pyruvate-dehydrogenase-(acetyl-transferring),-homodimeric-type
MNWLNEVLNNDPNPVETQEWIESLKAVIDVEGSERAHQLLEGMVELTRRSGAYLPFSPTTEYVNTIEPQLEAKSPGNAELEWRIRSIIRWNAMATVVRANRKPGDLGGHIASFASGATLYDVGFNHFWRAPSENHPGDLLFIQGHSAPGIYARSFLEGRISEEQLDKFRMEVDGGGLSSYPHPWLMPDYWQTPTVSMGLGPLAAIYQAQFMRYLENRGLIEKSDRKVWCFIGDGESDEPETLGAIALAGREGLDNLIFVVNCNLQRLDGPVRGNGKIIQELEGVFRGGGWNVIKLLWGGYWDALLAKDTNGVLKKLMMETVDGEYQNCKAFGGAYTREHFFGKYPETAAMVAGLSDDDIWRLNRGGHDPHKVYAAYHQAVNTKGMPTVILAKTVKGYGMGSAGEALNPTHQTKKLDDEAVRHFRDRFNIPVTDAQLADGQVPFYHPGPDSPEVQYLQERRAALGGYLPQRRRKADKTFVAPKLEAYDRLLKSSGERSYSTTMAFVQSLNITLRDKELGPHIVPIVADEARTFGMEGLFRQIGIYAPFGQKYKPVDADQLMFYREDQSGQVLQQGISEPGAISSWMAAGTSYSVSNVPMLPFYIYYSMFGFQRVGDIAWQAADMRTRGFLLGGTAGRTTLNGEGLQHEDGFSHLVAGGIPNVRSYDPTFGFEVTVILQHGTKRMMEDQVDEYYYVTLMNENYTHPEMPEGAAEGIVKGMYLLTDAGKPKKGELRVQLLGSGTILREAIAAAELLDKDFGVTADIWSCPSFNELRRDGFDVERANRLHPEGEQRKAYVTELLEGRQGPAIAATDYVRAYADQIRAFVPMSYTVLGTDGFGRSDTRANLRRFFEVDRYYIAHAAIAALAKEGKMTAKDVARAIKQYKIDPEKANPVGV
>NZ_CP047310.1|WP_159359709.1|433155_434562_+|AAA-family-ATPase
MKALKDVVPTPEQLALFSRVRPGVELIRGAAGSGKTTTALLKLKAAVGFYVNRVKRSPAKRQVKVLVLTFNRTLRGYIAELARSQFVEGNEISLEISTFSSWAKAMVGAGDVLGAAQSQGILQAFAAGGTIDPEFAAEEAMYVLGRFMPDQVDEYLSTKRVGRGLVPRMERTQRSVLLKSVVEPYVQHKKNHGLLDWNDLAVLAAEQSEEIYDVVVIDEAQDFSANEMRAVVAKLRGDHTICIVLDAAQRIYARSGFGWSEVGLHVKSENSFRLDVNYRNTKQIAAFATGILDGIDPGDDGALPDFTKAKVDGDLPVILKGTFGRQMDWVMQFISEKVDLSEESVAFLHPAGGGWFRHIRETLDNAGIGYAEISRKADWPDGAESIALSTMHSAKGLEFDYVIMLGISSENMPLDDESTDDEAHHRARRLLAMAVGRARRQVVIGYKPEQASEISAFFKDELCRVINL
>NZ_CP047310.1|WP_159359710.1|434558_435209_+|DUF4433-domain-containing-protein
MTIEDFCETRGVSRILHFTTNRGCIGVLHSRALRSRQRLTEDEQLKFVFQPNAASRTKDAAWLDYVNLSIERINNTFFGICSERWHDGRDNWWCVLQFSPEILTHPGVFFSTTNNIYTSVVRGEGVAGIAALYGDKVQRWYGNVVARPGDLPDAYTTCVQAEVLYPGEVSTSWLEAIHVRTSEESDEVAAQIRATGHRDVPVYVNGEIFGENVDEC
>NZ_CP047310.1|WP_159359711.1|435198_436806_+|ADP-ribosylglycohydrolase-family-protein
MSAKQPVSLKQIRNSMLWAAWGDAVGFPAELVSDREYSKRVGAKGWGGTPAWKKVVGGRFGVQVQLPAGAYSDDTQLRLATCRAIFTGGRFDVELFSKIELPIWLSYALGAGRGSKAAASSLTSNNVAWFSNFYSAKGIDYMYGGGNGAAMRIQPHVWSCADLSSPIAYMVDVVRNSVCTHGHVRGIIGAAIHARFLAYALMTRKIPPLNLWSELAHDAAESAVGAIDQDEQLSQIWLPTWEAKSGVAFCEAVEEVLREWEQLVLLAGDIRAETEDYRAAYRRLVDSCGGLDSSSRGSGILSALLSAAGSLWLDQAGERGALVEMGTLLGSDTDTIASMAGALIGACSSIEPPEVIQDREYLIQCADRLWRLSQSLAVDDFIYPDLLYWQPPKNALDVMSIKTKMIVVPGLGRVSPKDGKWVLRKGGVAFQWFEIWFGQTILCKYRIGAEDPAQRSHESVLIENTLPDLFVDKVDVGSVEAQIDNNIDALVSSVLDSNFNPGILGRILSEMIRSGRPVEDIVCFSALVTRSFRSR
>NZ_CP047310.1|WP_159360774.1|436878_437592_-|HNH-endonuclease
MEARLANGSALEKARVYRELAARHGRTSKAWEYRMQNISHVLDQAGKPWLPGLLPASNVGAKVEPKLAKLLGLSGETLTSVSGPTRGLLQQEAKTAEASGSFSSTDEVDERRRVLAAIVRRRGQPAFRKALLDAYGGRCAMTGCNVPDALEAAHIHPYSGLKSNDVRNGLLLRADVHTLFDLYLVTINPDSLRIAVAPALQNSAYVELEGKELTPASSNDVLASPESLTWHRSRCSW
>NZ_CP047310.1|WP_057499938.1|438256_438625_-|hypothetical-protein
MNTSDFRSLHAQYDPDNTEPDRERSIDPNAFVATLHRIGTGAAADGQPWPERHQLPGRCLQLADADCALAGLRVVAELMLAAERTRQNGAPEEYLGDRVMEGLKMACVALTAQVAERLHVRE
>NZ_CP047310.1|WP_159360775.1|439111_439333_-|hypothetical-protein
MPMTKIDPTWLEAFDKELLRLFAIDHRDAGMDEYLLGCYTDLPPREAALAFGNDYDLERDDALWPRPGVALQS

Crispr_ID: NZ_CP047310_3

• CRISPR_ID: NZ_CP047310_3
• CRISPR_location: 2091702-2091809
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP047310_3

Consensus_repeat	Method
ATCCACGCATGGCGTGGATCTACC	CRISPRCasFinder

spacers of NZ_CP047310_3

>3.1|2091726|60|NZ_CP047310|CRISPRCasFinder
GCAACCCGTTTTGGTGGGTGCTGACCTTGGTCGGCACGAATGCCTCCTGCACGCGCGACC

CRISPR arrays and Neighbor proteins around NZ_CP047310_3

CRISPR arrays

The CRISPR arrays of NZ_CP047310_3

>merge|NZ_CP047310|3|2091702-2091809|CRISPRCasFinder
ATCCACGCATGGCGTGGATCTACCGCAACCCGTTTTGGTGGGTGCTGACCTTGGTCGGCACGAATGCCTCCTGCACGCGCGACCATCCACGCATGGGGTGGATCTACC

>NZ_CP047310|3|3|2091702-2091809|CRISPRCasFinder
ATCCACGCATGGCGTGGATCTACC	GCAACCCGTTTTGGTGGGTGCTGACCTTGGTCGGCACGAATGCCTCCTGCACGCGCGACC
ATCCACGCATGGGGTGGATCTACC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP047310.1|WP_010485865.1|2094046_2094661_-|high-frequency-lysogenization-protein-HflD	unknown	unknown	gnl|CDD|234690
NZ_CP047310.1|WP_010485880.1|2083652_2084873_+|two-component-sensor-histidine-kinase	unknown	unknown	gnl|CDD|340419
NZ_CP047310.1|WP_010485856.1|2096845_2097172_+|ATP-dependent-Clp-protease-adapter-ClpS	unknown	unknown	gnl|CDD|178809
NZ_CP047310.1|WP_159360117.1|2083222_2083561_+|flagellar-protein-FlgN	unknown	unknown	unknown
NZ_CP047310.1|WP_010485887.1|2081063_2082008_-|chemotaxis-protein-CheV	unknown	unknown	gnl|CDD|381151
NZ_CP047310.1|WP_010485859.1|2096259_2096733_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP047310.1|WP_049481290.1|2086667_2088770_-|PAS-domain-containing-sensor-histidine-kinase	unknown	unknown	gnl|CDD|226951
NZ_CP047310.1|WP_019337423.1|2084890_2086663_-|EAL-domain-containing-protein	unknown	unknown	gnl|CDD|238923
NZ_CP047310.1|WP_159360122.1|2097276_2098089_-|APH(6)-family-putative-aminoglycoside-O-phosphotransferase	unknown	unknown	gnl|CDD|226100
NZ_CP047310.1|WP_010485889.1|2080511_2080907_-|flagellar-basal-body-rod-protein-FlgB	unknown	unknown	gnl|CDD|183628
NZ_CP047310.1|WP_159360118.1|2088901_2091661_+|EAL-domain-containing-protein	unknown	unknown	gnl|CDD|236645
NZ_CP047310.1|WP_159360120.1|2094657_2095800_-|tRNA-2-thiouridine(34)-synthase-MnmA	unknown	unknown	gnl|CDD|234664
NZ_CP047310.1|WP_071306143.1|2100581_2100959_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP047310.1|WP_010485867.1|2092692_2093883_-|chemotaxis-protein	unknown	unknown	gnl|CDD|206779
NZ_CP047310.1|WP_159360121.1|2095796_2096258_-|NUDIX-domain-containing-protein	unknown	unknown	gnl|CDD|239647
NZ_CP047310.1|WP_010485884.1|2082188_2082845_+|flagellar-basal-body-P-ring-formation-protein-FlgA	unknown	unknown	gnl|CDD|183625
NZ_CP047310.1|WP_019337421.1|2082920_2083226_+|flagellar-biosynthesis-anti-sigma-factor-FlgM	unknown	unknown	gnl|CDD|274802
NZ_CP047310.1|WP_049481282.1|2098227_2100513_+|ATP-dependent-Clp-protease-ATP-binding-subunit-ClpA	unknown	unknown	gnl|CDD|236828
NZ_CP047310.1|WP_010485892.1|2080100_2080508_-|flagellar-basal-body-rod-protein-FlgC	unknown	unknown	gnl|CDD|183634
NZ_CP047310.1|WP_010485869.1|2092378_2092594_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP047310.1|WP_010485865.1|2094046_2094661_-|high-frequency-lysogenization-protein-HflD	gnl|CDD|234690	PRK00218, PRK00218, lysogenization regulator HflD.	1.23642e-86
NZ_CP047310.1|WP_010485880.1|2083652_2084873_+|two-component-sensor-histidine-kinase	gnl|CDD|340419	cd16943, HATPase_AtoS-like, Histidine kinase-like ATPase domain of two-component sensor histidine kinases similar to Escherichia coli K-12 AtoS. This family includes the histidine kinase-like ATPase (HATPase) domains of various histidine kinases (HKs) of two-component signal transduction systems (TCSs) such as Escherichia coli AtoS, an HK of the AtoS-AtoC TCS. Proteins having this HATPase domain also contain a histidine kinase dimerization and phosphoacceptor domain (HisKA); some have accessory domains such as HAMP or PAS sensor domains or CBS-pair domains.	2.03429e-52
NZ_CP047310.1|WP_010485856.1|2096845_2097172_+|ATP-dependent-Clp-protease-adapter-ClpS	gnl|CDD|178809	PRK00033, clpS, ATP-dependent Clp protease adaptor protein ClpS; Reviewed.	9.35868e-44
NZ_CP047310.1|WP_010485884.1|2082188_2082845_+|flagellar-basal-body-P-ring-formation-protein-FlgA	gnl|CDD|183625	PRK12617, flgA, flagellar basal body P-ring formation protein FlgA.	2.96267e-108
NZ_CP047310.1|WP_010485887.1|2081063_2082008_-|chemotaxis-protein-CheV	gnl|CDD|381151	cd19924, REC_CheV-like, phosphoacceptor receiver (REC) domain of chemotaxis protein CheV and similar proteins. This subfamily includes the REC domains of Bacillus subtilis chemotaxis protein CheV, Myxococcus xanthus gliding motility regulatory protein FrzE, and similar proteins. CheV is a hybrid protein with an N-terminal CheW-like domain and a C-terminal CheY-like REC domain. The CheV pathway is one of three systems employed by B. subtilis for sensory adaptation that contribute to chemotaxis. It is involved in the transmission of sensory signals from chemoreceptors to flagellar motors. Together with CheW, it is involved in the coupling of methyl-accepting chemoreceptors to the central two-component histidine kinase CheA. FrzE is a hybrid sensor histidine kinase/response regulator that is part of the Frz pathway that controls cell reversal frequency to support directional motility during swarming and fruiting body formation. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	1.30475e-37
NZ_CP047310.1|WP_049481290.1|2086667_2088770_-|PAS-domain-containing-sensor-histidine-kinase	gnl|CDD|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	3.84698e-42
NZ_CP047310.1|WP_019337423.1|2084890_2086663_-|EAL-domain-containing-protein	gnl|CDD|238923	cd01948, EAL, EAL domain. This domain is found in diverse bacterial signaling proteins. It is called EAL after its conserved residues and is also known as domain of unknown function 2 (DUF2). The EAL domain has been shown to stimulate degradation of a second messenger, cyclic di-GMP, and is a good candidate for a diguanylate phosphodiesterase function. Together with the GGDEF domain, EAL might be involved in regulating cell surface adhesiveness in bacteria.	5.40463e-97
NZ_CP047310.1|WP_159360122.1|2097276_2098089_-|APH(6)-family-putative-aminoglycoside-O-phosphotransferase	gnl|CDD|226100	COG3570, StrB, Streptomycin 6-kinase [Defense mechanisms].	6.04889e-77
NZ_CP047310.1|WP_010485889.1|2080511_2080907_-|flagellar-basal-body-rod-protein-FlgB	gnl|CDD|183628	PRK12620, flgB, flagellar basal body rod protein FlgB; Provisional.	5.39936e-79
NZ_CP047310.1|WP_159360118.1|2088901_2091661_+|EAL-domain-containing-protein	gnl|CDD|236645	PRK10060, PRK10060, cyclic di-GMP phosphodiesterase.	1.52744e-105
NZ_CP047310.1|WP_159360120.1|2094657_2095800_-|tRNA-2-thiouridine(34)-synthase-MnmA	gnl|CDD|234664	PRK00143, mnmA, tRNA-specific 2-thiouridylase MnmA; Reviewed.	0
NZ_CP047310.1|WP_159360121.1|2095796_2096258_-|NUDIX-domain-containing-protein	gnl|CDD|239647	cd03675, Nudix_Hydrolase_2, Contains a crystal structure of the Nudix hydrolase from Nitrosomonas europaea, which has an unknown function. In general, members of the Nudix hydrolase superfamily catalyze the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+, for their activity. They also contain a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which forms a structural motif that functions as a metal binding and catalytic site. Substrates of nudix hydrolases include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance & "house-cleaning" enzymes. Substrate specificity is used to define families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required.	1.94626e-70
NZ_CP047310.1|WP_049481282.1|2098227_2100513_+|ATP-dependent-Clp-protease-ATP-binding-subunit-ClpA	gnl|CDD|236828	PRK11034, clpA, ATP-dependent Clp protease ATP-binding subunit; Provisional.	0
NZ_CP047310.1|WP_019337421.1|2082920_2083226_+|flagellar-biosynthesis-anti-sigma-factor-FlgM	gnl|CDD|274802	TIGR03824, FlgM_jcvi, flagellar biosynthesis anti-sigma factor FlgM. FlgM interacts with and inhibits the alternative sigma factor sigma(28) FliA. The C-terminus of FlgM contains the sigma(28)-binding domain.	3.49375e-14
NZ_CP047310.1|WP_010485892.1|2080100_2080508_-|flagellar-basal-body-rod-protein-FlgC	gnl|CDD|183634	PRK12629, flgC, flagellar basal body rod protein FlgC; Provisional.	6.04545e-81
NZ_CP047310.1|WP_010485867.1|2092692_2093883_-|chemotaxis-protein	gnl|CDD|206779	cd11386, MCP_signal, Methyl-accepting chemotaxis protein (MCP), signaling domain. Methyl-accepting chemotaxis proteins (MCPs or chemotaxis receptors) are an integral part of the transmembrane protein complex that controls bacterial chemotaxis, together with the histidine kinase CheA, the receptor-coupling protein CheW, receptor-modification enzymes, and localized phosphatases. MCPs contain a four helix trans membrane region, an N-terminal periplasmic ligand binding domain, and a C-terminal HAMP domain followed by a cytoplasmic signaling domain. This C-terminal signaling domain dimerizes into a four-helix bundle and interacts with CheA through the adaptor protein CheW.	6.0076e-31

Protein sequences

>NZ_CP047310.1|WP_159360118.1|2088901_2091661_+|EAL-domain-containing-protein
MDQGIIASLLQHPLASALVIVDRTGRPLAANPAAREHGLPATVAAYAPMLEDLRLMAADGGIVACTLPGGPHGHYDGHLRAVHDGAGNLLAFTLSIPEPVPLGGGGRWELALDSAGHSLWDWDIPSDRVVRTPALGDETATEILARVHSEDIAQVRVALDEHLRGLSEQYSAQFRFRQADGQWRWVLDRGRVVARTADGQPLRMVGTHTDIEQQKQLEGLLQEQQLHLSEAQRIASMGSWSFDPNSGHFWWSPELRSMLALEQGSAPGQRRWMKQLHPRSRGALRAAWRRLWRDGRAANIELELTRGHEPSQHLRLWMQPLLDMDGQPKRLLGQVQNITEQHQTDALIRWRTELLNRVSALGRIGGCEIEVQTRHMQWTEECYRIHGLRKEPITLDQALALYTEDSRNAFEAALGRIADGGLPEQLDLCFYRQSGLRVWVQVLIELDRRDGLPPRFVVLFRDITREREANERIELLAHYDLLTGLPNRVLLGEQTAEAIEEARDRGTSLAMLFIDLDGFKTINDSFGHATGDALLKAAATRLHQNLRNNDLFGRFSGDEFIVVLRDLAEPEDAGHVARKLIASLAEPLRRGETTLKVGASVGIAMLGDAQTDFDSLLRAADAAMYAAKEAGRNTYQYYSQDALARIQRKLELEHALHGAIEREEFSLAYQPLLHAHHGEPPAIEALLRWHRPGIGYCSPAEFIPIAEKCGEIVRIGDWVLNEACRQATAWDRAGLRFDRIAVNVSAVQLRDRGFAERVIEICHAHGWPPQRLELELTESALIRDTDILRHCFDVLERHGVPLAVDDFGTGFSNLNYLNRFPVGRLKIDRSFVQGMLHDSGTAEVTQAIVHLGHALGMKVVAEGVETHQEEDMLRRQGCDEIQGYLYSRPLSPRDLAQWLRQPQPVSLRTDASGEVVLVR
>NZ_CP047310.1|WP_049481290.1|2086667_2088770_-|PAS-domain-containing-sensor-histidine-kinase
MPAEPTGNAPVPDPRMAQALSRDRRRVVLSYLAMALAWMISTDSAVQALVPDPQQAALWQGLKGSFFALASAGLLYLLLRPLAEHVLHTHARQQASELRLRQMFEGNPGPILVYDLDTLAILDANPAACTAFGWDRDELLEQTIDALWPPGQDQALQTKLEAIREAPEELCILRTQLQLRDGSLRQMELRSNAISYDGHNARLLIAIDRTAEDLAQLRRDQALARVEEAHELARIGAWELDPSTGLGRYSNQVYRLLGRRPPEARRWHRFDELLVPADPATATQTEQLLAELCSGDPVHVDVLLPLLSMDGRALMVHLRAASGIDEAGRNRVLGTLQDVTEREQSRRLLREREEQFRELVRVLPDGVVILSDEHVLYANAWAASLFGYGSHTLLGEPLSALVDNADLSRVRSQLRAGQPHLGPGHSSVVVMQRADGRSFHAGLAVGEVRYGGRDCKLLIVRDLSDSERTRSALETSNRELQAMAGRLFSLQEDERRAISRDLHDDIGQAITAIKLSAYAAQDEDDPQRRAEDLAQIVSLADTTVAKLRDISTLLRPPQLDALGLEAALSWQARVLFRSSPVELLAEIEPLPHRPDNSIEQACFRIAQESLTNVLRHARASQVQLQLRDVGQRGLHLQIRDDGEGFDPDGPRGLGLIVMRERAQSVGGHVRIESAHGEGTLIDVHLPYQAASMAAVESPEY
>NZ_CP047310.1|WP_019337423.1|2084890_2086663_-|EAL-domain-containing-protein
MWNPNQPPVSIDDAPDRLGAGNPELQVMVAEAASGGTALMLMHVDIDHFASVNENMSAEVGDQALALVAQRLQSYLRGRGKLWRHGSDEFLIAVPRTADVPLPEDFAEEIRQQMELPLSVLPYTLFMTGKLGVSLCPDHASSASRLLDHAEDALYQAAREGGNAVRIHAVDTPPSAHSESIIARQIVDAIPNGELKLRYQPLVSARDGHVVGMEALLRWQSPTLGMLVPERFMRTAERLGIIVQIGTWVLEGALKQARLWRDQGFDDFTIAVNVSTLQLLRPNFFAEVMGLIQAAGVPAQMLTLEINESALTNNVNFVHETLANLRNEGISLSLDNFGTGDSSLSALVRYPVDKLKIDRSFIKSAPAGNREAAIARAIIAMGHQLGMTVIANGVESQAQLGFLRRNDCDVFQGYLFGEPMSADAAGMTLRRRYLRPEAFAETRPDRTLLLLDDEENVLRSLVRLFRRDGYRILAAGNVRDAFDLLAINDVQVILSDQRMSDMSGTEFLGRVKMLYPDTIRLVLSGYTDLNTVTDAINRGAIYRFLTKPWNDDELRKHIHQAFRTYEEQRRSNAGPAPVESGDGGEDRPLR
>NZ_CP047310.1|WP_010485880.1|2083652_2084873_+|two-component-sensor-histidine-kinase
MSAANALVTAPLPPQPVLQALLERLREGLLLFTDDGQVALANPAAQNLLASGEGGGLPPPQRLRELLPPDALEQARQHGHWNGSLPLGEGVVIAHLYHHGPVGQGHFLALFRHIEGQEDYERELQQRHAELRQAYLRLNGTQEKLLQSEKMASIGQLAAGVAHEINNPIGYVHSNLGSLQEYLRSLFTVIEAYERALRAPDPKALIPEIDDIRDRLDIDFISRDLPQLMAESREGIERVTRIVRDLKDFSYSGRDESWKLVDLHAGLESTINIIWNELKYKVTLVREFGQLPLVECLPSELNQVYMNLLLNAGHAIAERGTITVRTGVDGDHVWVEFEDTGGGISPELRQRIFDPFFTTKPVGSGTGLGLSISYSIINKHHGRIDLDSTPGVGSRFRVVLPVKQPR
>NZ_CP047310.1|WP_159360117.1|2083222_2083561_+|flagellar-protein-FlgN
MTAAMSEPLQRLAQALDVERQALVEHDVHALIRATGAKLEALRALEGAPPVGEGEQLRELAERNRANGVLLSRRRREVNWALRQLGRTEDASAYDAKGQAHTVTARRPLAVA
>NZ_CP047310.1|WP_019337421.1|2082920_2083226_+|flagellar-biosynthesis-anti-sigma-factor-FlgM
MSQKIDGNLQVPQALRSVTTPANKPGVSTDAAARPVEAADSLRLTGEATNLQAIERELTTAPAIDAQRVAAVRESLQNGTYKINPDAIASRMLELDQQLHG
>NZ_CP047310.1|WP_010485884.1|2082188_2082845_+|flagellar-basal-body-P-ring-formation-protein-FlgA
MRRVTSLFAIALALASPWAVAADWQPVASIRAAALSTLPAGSEGEAQVADALRLPRCGGALQVQPTANTTVEVSCPDAGGWRLFVPVKVRRNQTVLVLNRGIGTGETLTAADITTAQRDAARIAGAVLADPNAAIGRIARRPLQAGALLSNNDLVVQRLIKRGDNVALVSRRGSVEVRIAGRAMGDAGENERVSVENLSSRRIVQGTVDAAGDVIVAR
>NZ_CP047310.1|WP_010485887.1|2081063_2082008_-|chemotaxis-protein-CheV
MSHDLLNRIDQRTRLAGHNRLALLLFRLGGRQLFGVNVFKVQEVLRRPELFQVPGLPSQFSGVADVRGRSVPVLDLGLAIGHPEREPDADTSPGYLVVTEFNRSIQGFLVSGVERIVNIAVEDIHPPPELGAESSYLTAVTRFQGELIQVIDVESVLADIAQVRGEAVLDPTMAMPADGPQLQVLVVDDSRVARQQIRSVLDQLGVGATLLSDGKQALDHLLQIHASGENPAERYAMVISDIEMPAMDGYTLTTEIRRHPGLAGLYVLLHTSLSGVFNNAMVERVGANAFVAKYSPHELADFVLDRLRKVAMAA
>NZ_CP047310.1|WP_010485889.1|2080511_2080907_-|flagellar-basal-body-rod-protein-FlgB
MRNLITDYLGVHAQAMPLREQRMKLIASNLGNADTPGYKAQDLDFDAALRHAQGQDANGLMTTTNEQHYEISSGLNPFQIARDGVQPSLDGNTVDPDAERAAYGRAALEYRASLSFVESKVRSMLTAITGQ
>NZ_CP047310.1|WP_010485892.1|2080100_2080508_-|flagellar-basal-body-rod-protein-FlgC
MSNLPIFDIAGSALQAQSVRMSTIASNLSNADTVAGSADAVYKPLEPIFQAVTSKNDPNITSVKVKEITQSEAAPIKRYEPGHPLADGDGYIYQPDVDPVAQMVNLISTSRNYQAGVEMLTTAKELALATLTMGR
>NZ_CP047310.1|WP_010485869.1|2092378_2092594_-|hypothetical-protein
MTLIHALPSLTNTERPRNASVREQLQQLEEVAREEIRELQQLADARPAPSRADEALLGLAWDLGLDGEALR
>NZ_CP047310.1|WP_010485867.1|2092692_2093883_-|chemotaxis-protein
MYSRIFIRLAAPLALTLLLPFAIGFEWPAALRWAILTTMTLSWLGFAWWTTRAQAHRSPEHARVLREQDQLLTELRNFVGNEIDGSRGEVERARDLIRQAVSSLGGSFDAMNRKSRQQSQALSRIVDRAGDEGNAGLDVARFAQHASHRMEQLVEALEQVSGQSSTTVQHIDQMAQHLDGIFALLEDVKSIADQTNLLALNAAIEAARAGEAGRGFAVVADEVRNLSERSTTFNEQIRKLAHSSKDAIAKVRETVSHMASRDMDRSREARQEAAAMLDNVAQINASLGDGMREVSECARSIDGSVAEAVRALQFEDIATQALGGVHTHLDRLTAINREAVALQELLHRNGGVFDEEIATALQRTGSRLRELRSEWERPPHKPVAQQSMGAGTVELF
>NZ_CP047310.1|WP_010485865.1|2094046_2094661_-|high-frequency-lysogenization-protein-HflD
MSFTVDDRVLALAGIAQALQQVRRIADTGHSDAAAVRTAVDSVFRVDASSPQEVFGDRHALKAGLRLLHNYFRSQGQDPILPKLALSVLQLERRFVQDGATVNKVASGIERAQRQATELGDSGHPDVLANLGGLYADTISHLKPRVMVQGNPHYLGQAGVVAEIRALLLAAVRSAVLWRQLGGSYWDFLFSRKAMIEAVDRQLA
>NZ_CP047310.1|WP_159360120.1|2094657_2095800_-|tRNA-2-thiouridine(34)-synthase-MnmA
MSTPRVMVGVSGGVDSSVAAWRLVQQGEAVAGLFMQNWADDGSGDCRAEDDRRDAVAVCGLLGIPFHFRDFSSEYWQGVFEHFLAEYAAGRTPNPDVLCNREVKFKHFLDAARELGAERIATGHYARVTQRGHQWLLLRGADRSKDQSYFLHQLGQEQLAATLFPIGDLEKTDLRRIARDVSLPTHAKKDSTGICFIGERDFREFLGRYLPAKPGQILDPADGSVIAEHPGVFYFTLGQREGLNIGGVRGRPAAPWYVVGKDVASNVLYVDQDRDSKWMLSDRLRSETAHWIAGAPPARRFECTAQTRYRQPDEPCTVEVLDDGSVLVTFARPQRAVTPGQSLVLYDGDECLGGAVIAATDAPLEQRLRTTPSPFEVIAA
>NZ_CP047310.1|WP_159360121.1|2095796_2096258_-|NUDIX-domain-containing-protein
MNATPDPRWAPHATVATVVVDGGRVLLVEETIDGRQVLNQPAGHLEPGESLAEAALRETREETGWTVQLTHFIGCYQWAAGDGTTFLRFCYAARPVSHDPAQPLDTGIDRALWLTPAELQAAGERQRSPLVWQVVADYLGGQRHPLSLVREVA
>NZ_CP047310.1|WP_010485859.1|2096259_2096733_-|hypothetical-protein
MKRTLLSALLIALAAAGSAAAETQADKAVARHLDKLGYTYEVDEDGDYRMVFDVEGDRTQMVYVRSSVEDFGTHNIREIWSPAYNAKTKQFPVAVANRLLEDSQDAKMGGWVKQDTTAMFVVKIDADATADQLSDAIDAAIRTADAMELELTKKDEF
>NZ_CP047310.1|WP_010485856.1|2096845_2097172_+|ATP-dependent-Clp-protease-adapter-ClpS
MPRESSPDSHHEHGVAVEPARPEVAPPPFYQVMLLNDDYTPMDFVVDVLQQFFSMDLDKATQVMLHVHTRGRGVCGVFTREVAETKVAQVNEYSRMNQHPLLCTMEKA
>NZ_CP047310.1|WP_159360122.1|2097276_2098089_-|APH(6)-family-putative-aminoglycoside-O-phosphotransferase
MSEPYLSRWRLRRDGAAIETPHAQLWPVLTIAGEPAMLKISSETEEQNSHRLLRWWEGDGAARLLAHEGPAILIERAGGDSLRQRSIEGDDDACTTILCQVLQRLHRPRSAPPAELVCLRRWFADLLQPRAALPPLLEQCRSLAEGLLQEEREIRPLHGDLHHDNVLDFGARGWLAIDPKRLLGDRAFDYTTLFSNPDLCGPGIHVATQPERFAARLEQVSALAGLERTRLLRWIAASAGLSAVWFRDDGAPAEVDEALARMALEALAEA
>NZ_CP047310.1|WP_049481282.1|2098227_2100513_+|ATP-dependent-Clp-protease-ATP-binding-subunit-ClpA
MFSKDLEHTIGQCYKRAREARHEFMTVEHLLLALLDNPSAQAVLKACGADAERLRQELEQAIEASVSRLAEDDGRDTQPTLGFQRVLQRAVYHVQSSGKKEVTGANVLVAIFGEKDSHAVYYLNQQDVTRLDVVNYLSHGIAKLGEEGEQPSSSSEGEGRIEGGEGEPKGDALTEFASNLNEQARAGRIDPLVGRADEIERTIQVLCRRRKNNPLYVGEAGVGKTAIAEGLARRIVEGSVPEVLADAVIYSLDLGALVAGTKYRGDFEKRLKSVLTALKKVPNAVLFIDEIHTIIGAGSASGGTMDASNLIKPALASGELRCIGSTTFQEYRGIFEKDRALARRFQKIDIVEPTVGETYEILQGLKSKYELHHGVTYSDEALQAAVDLSVKHIGDRLLPDKAIDVIDEAGARQRLLPEEQRKELIDVEEVEAIVAKMARIPAKQVSATDKDVLQHLERNLKMVIFGQDPAIETLSSAIKLARSGLGNPEKPIGNFLFAGPTGVGKTEVTKQLALQLGIELVRFDMSEYMEPHSISRLIGAPPGYVGFDQGGLLTEKIVKTPHCVLLLDEIEKAHPDIFNILLQVMDRGVLTDTNGREANFKNVVLVMTTNAGAAQASRRSIGFTKQDHATDAMETIRRSFTPEFRNRLDAVVQFQALGFEHILRVVDKFLIELEMLLQDKHVSLSATPTARDWLAHHGFDPLMGARPMARVIQDKIKRPLADELLFGKLVNGGKVSIDVRDDELVVETQAEPERLLPVTVE
>NZ_CP047310.1|WP_071306143.1|2100581_2100959_-|hypothetical-protein
MNLSSLLIPLALSAATLLASPAHAADTPPAQCVPLTGEQQIVRAGADKNILLRSGEDHYVVHFRNSCPSAVLATRLGFKTDGKEAGELCSEGRSALDTGRGSCEVARIELIDAERFKREARRRSR

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	572252 : 584892	10	Enterobacteria_phage(37.5%)	NA	NA
DBSCAN-SWA_2	2147610 : 2154774	11	Stenotrophomonas_phage(100.0%)	capsid	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP047310|572252:584892|DBSCAN-SWA
ATCAATCTTCAGAGACATTCGAATGCGTGCCCTGCCACGTGTCTTGCCAGATGATGAACTGGGGACGGCGCTTCGATTCGCTGTGGATGCGGCCGATGTAGAGGCCGACCACGCCCAGGCTGCCCATGATGAAGCTGCCCACTAGCCAGATTGAAGCGAGTATGCTGGTGAAGCCCGCCACCCTGATGTCACCGGCCCAGTAACGGTAGACCGCCAGAAGTGCGATGCCCGCACCGATGGCGGCCAGTGCAAATGCCGCCGTCATGACCAGTCGCAGGGGCTTGTCGGAGAACGACAGCGCGATCCGGGTCGCCATCTGCAGGAGCTTGCGCAGCGTGTAGCCACTCTTGCCCTCCGTACGACGACCATGCGACACCGGTACGCGCAGGGTTTTAAAACCAGTCCAGCGGGCCATCAGAGGGAGGAAGCGATCCGTCTCAGGCATCGCATTCATGGCATCAACAGCCTTGCGGCTGTAGGCACCGAAATTGGCCGTCGAAGGATCATAGTCGGTATCGGTCAGCCATCCCAGTGCCTTGTAGAAGGCACTGGAACCGCTTCGCTTCAGCCAGGTGTCCTGGCGTTCCACCCGCTGGCCCAGCACGATCTCGTTGTCACCTTCCAGGCCTGCCAGCAGCGAGGGAATTTCCTCGGGGACATCCTGTAGGTCACAATCCATGACAATGACACGGCTGCCCTGGGCGTACTGCAGCCCGGCACTGATTGCCGCATGCTGTCCGAAGTTGCGGGACAGGCGCAGGCCGCGAACCCGGGAAGACAGCTTCCCGAGTTCGCAGATCCGCTGCCAGGACTGATCGGGACCCTGGTCGTCCACGAGGATCAGTTCGTGCGTCAGGCCCATGCCCGAGATCGCACCGGCAACACGTTCGGAAAGCTGTTCAAGGCAACCTTCACAACCGTACACGGGCACCACCACCGAAACGTCGGGGGTGGGGCCACTGTCCGGGGGATTCTGATTGCCTGCCTCAGCGCGCATGGCGTACTCACCCATGATGGAAGCCGGAGTCCAGATTCAAAGTGCTGCTTCCAGCTCCGGCAGGATCGCAAACAGATCCCCCACCAGACCGATATCGGCAATCTCGAAGATCGGCGAATCCGCATCCTTGTTGATCGCCACGATCGTGCCGGCATCCTTGATGCCGGTCAGGTGCTGGATCGCACCGCTGATGCCGACGGCTACATACAGTTCCGGCGCGATGATCTTGCCGGTCTGGCCGACCTGCAGGTCGCTGGGCACGTAACCGGCGTCGACCGCGGCACGCGAGGCACCCACGGCGGCACCGAGCTTGTCGGCCAGCTGGAAGATGACCTTGAAGTTCTCTTCCGAACCGACGCCACGGCCACCGGAGACCACGCGCTTGGCGCTCTGCAGGTCCGGGCGGTCGCTGGCACCGGCGGCCAGACCGACGAAGCGGGTGTGGGTCGGCAGGGCAGCGTCAACGCTGGCCGCTTCGACGGCGGCGCTGCCGCCCTGGGCAGCTTCCGGCCACGAGGCAGCACGCACGGTCGCGACCACGATCTGGTCGGCCGGTGTTTCCACGGTGATGATCGCGTTGCCGGCGTAGATCGGGCGCTTGAAGGTGTGGCTGCCTTCGACGCTCATCAGGTCGGAGACCTGGTTGACGCCCAACAGGGCAGCCACACACGGCATCAGGTCCTTGCCGAAGGTGGTCGACGGGCCGAACACGTGGGTGTAGCCCTTGGCCAGCTGCGCGATCTGCGGCGCCAGTACCTGGGCGATGGCCTGCGCGTTGGCGGCATTGGCCACGGTCAGGACCTTGGCGACGCCAGCGATCTTCGCGGCTTCGGCGGCGACGGCGGCCGGGTCGGCGGCCAGCACCAGCACGTCGATGCTGGCACCGCTGATGGCGGCGGCGGCACTGACGGTCTTGGCGGTGGCGGCGTTGAGCTTGCCGTCGTGGTGCTCGGCGATGACGAGAATCTTGCTCATTACAGCAGCCCCTTCTGCTTGAGTGCGGCAACCAGTTCGGCCGCGTCCTTGACCATCACACCCTTGCTGCGCTTGGACGGCGCGGCGTACTGGGTGGTCTTGAAGGTGTCGGCGGCTTCAACGCCGAGGTCGGCCAGCTGCAGGGTTTCCAGCGGCTTGGCCTTGGCCTTCATGATGTCCGGCAGCTTGATGAAGCGCGGCTCGTTCAGGCGCAGGTCGGTGGTGACCACGGCCGGCAGCTCCACTTCAAGTGTTTCCAGGCCGGCGTCGACTTCACGGGTCACCGTGGCCTTGCCATCGGCAATCTCCAGCTTGCTGGCGAAGGTCGCCTGCGGGCGGCCCCACAGCGTGGCCAGCATCTGGCCGGTCTGGTTGGCGTCGTCGTCAATGGCCTGCTTGCCGAGGATCACCAGGTCCGGCTGTTCCTTCTCGATCAGCTTGAGCAGGGTGCGCGACGCGGTCAGCGGCTGGATGGCCTGGTCGGTGACGACATGGATGGCGCGGTTGGCGCCCATGGCCAGGCCGTTGCGCAGGTGCGCCTGGGCGTCGGCCGGGGCGATGGTGGCAACCACGACTTCGCTGGCGATGCCCTTGTCGCGCAGGCGCAAGGCTTCTTCCAGGGCGATTTCATCGAAGGGGTTGGGGGACAGCTTGACGCCGTCGGTGACCACGCCGGAACCGTCCGGCTTGACCTGAATGCGGACGTTGTAGTCCACCACGCGCTTGTACGCGACGAGGATTTTCATCTGGTACGGGGTCCTTCAGTAACAGGGAGAACGTCCGGTCCTGCAACAGCAACCGGTTCGGGGGTGGGACCCCGATTCTAGCTGGCTTGGGGTGACCATGCGAATGCGTATGGTTATGTTGCGGCGCCGCAAGAATGAACCTCCGCGAGCTCGTGTTCACGTCACGCAGGCGGTCGTGAAGGCCATCGGGATGTATCCTGTGACGCTGCGCTGGGGCGCCCGTGGGCGCTCCTTGGATGAATTTAGATCAGGAGAACAGGTAGTGCCCACATGGCTTGTCACCGGCGGCGCCGGATTCATTGGCGGTAACTTCGTTCTCGAGGCCGTCGCACGCGGCGTCAAGGTCATCAATCTCGATGTGCTGACCTACGCCGGCAACCTGAGGACCCTGTCCAGCCTGGACGGCAACCCCAACCACCTGTTCGTGCAGGGCGATATCGGCGACCAGGCCCTGGTCGCGAACCTGCTGGCCGAACACCGGCCGGATGCCGTGGTGAACTTCGCCGCCGAAAGCCACGTTGACCGCTCCATCGACGGTCCCGGCGCCTTCATCCAGACCAATGTGGTGGGCACCCTGGGCCTGCTGGAAGCGGTCCGTGACTACTGGAAGGCGCTGCCGGCCGAACAGGGCGCGGCCTTCCGCTTCCTGCACGTGTCCACCGACGAGGTGTACGGCACCCTGGGCGAGACCGGCAAGTTCAGCGAAACCACACCGTACGCCCCGAATTCGCCGTACTCGGCGTCGAAGGCCGCTTCGGACCACCTGGTCCGTGCCTTCCACCACACCTACGGGCTGCCGGTACTGACCACCAACTGCTCCAACAACTATGGCCCGTACCACTTCCCCGAGAAGCTGATCCCGCTGGTGATCGCCAAGGCGCTGGCTGGCGAGCCGCTGCCGGTGTACGGCGATGGCAAGCAGGTGCGCGACTGGCTGTTCGTGTCCGACCACTGCGAAGCGATCCGCACCGTGCTGGCCAAGGGCCAGGTCGGCGAGACCTACAACGTCGGCGGCAACTCGGAAAAGCAGAACATCGAAGTGGTGCAGGCCATCTGTGCGCTGCTGGACCAGCGCCGCCCGCGCGCGGATGGACAGCCGCGCAGCAGCCAGATCACCTACGTCACCGACCGCCCCGGCCATGACCGCCGCTATGCGATCGATGCCTCCAAGCTGAAGAACGACCTGGGCTGGGAACCGGCCTACACCTTCGAGCAGGGCATCACGTTCACCGTCGACTGGTACCTGGACAACCAGGAATGGATCAACGGCGTGCTGGATGGCAGCTACCGTCTGCAGCGCATCGGCACTGCCGCCTGAGGCCGGGAGATAACATGACGCAACGCAAGGGCATCATCCTGGCCGGCGGTTCCGGCACCCGGCTGTATCCGATCACCAAGGGCGTCAGCAAGCAGCTGTTGCCGGTGTACGACAAGCCGATGATCTACTACCCGCTCAGCGTGCTGATGCTGGCGGGCATCCGCGAAGTGTTGATCATCAATACTCCGCACGAACAGGCGCTGTTCCAGCAGCTGCTGGGCGACGGTTCGCAATGGGGCATGGACATCCAGTACGCGGTGCAGCCGAGTCCGGATGGCCTGGCCCAGGCCTACCTGATCGGCCGCGACTTCGTCGCCGGCAAGCCGAGCTGCCTGGTGCTGGGCGACAACATCTTCCACGGCCACGGCCTGCGCGAGGTGCTCAAGCGTGCAGACGAACGCGTGCACGGCTCGACCGTGTTCGGCTACTGGGTGAATGATCCGGAGCGCTACGGCGTGGCCGAGTTCGACCAGAGCGGCAAGGTGATCGATCTGGTGGAGAAGCCGGAGAAACCGCGCTCCAACTATGCGGTGACCGGCCTGTACTTCTATGACGGCAAGGCCAGCGATTACGCGGCCGAACTGAAGCCGTCGCCGCGTGGTGAGCTGGAGATCACCGATCTCAACAAGCGCTACCTGGAAGAAGGCAATCTTCACCTGGAAGCGCTCGGCCGTGGCTATGCGTGGCTGGATACCGGCACTCACCAGTCGCTGCTGGAAGCCTCCAACTTCATCGAGACCATCCAGACCCGCCAGGGCCTGCAGGTCTGCTGCCCGGAAGAAATCGCCTTCGGCAAGGGCTGGATCACCGCCGAGCAGCTGGAAGCACTGGCTGCGCCGCTGATCAAGAATGGCTACGGCCAGTACCTGCACAAGCTCGCTCTGCGTGGAGTCGTTCCGTGAAAGTGATTGAAACCAAGTTGCCCGGCTGCGTGGTGATCGAACCGGCCGTGTTCGGTGACGCGCGCGGTTACTTCTTCGAAACCTGGAATGCCGAGCGTTTCGCCGCGCTGGGCCTGCCGGATCGTTTCGTGCAGAGCAACGTGTCCACCTCGGCGCAGGGCGTGCTGCGTGGCCTGCATTACCAGTGGCCGCGCCCGCAGGGCAAGCTGGTCAGCGTGCTGGAAGGCGAGGTCTATGACGTGGCCGTGGACATCCGCCGCGGCTCGCCGACCTTCGGCCAGTGGGAAGCGGTGGTGCTGAGCGCGGAGAACAAGAAGCAGTTCTGGATTCCGGAAGGCTTCGCCCACGGTTTTGCCGTACTGTCCGAGCGCGCGGTGTTCAGCTATCTGTGCACCGAGGTCTACCTGAAGGACTTCGACGCAGGCGTGCGCTGGAACGATGCAGATATCGCCGTGGACTGGCCGGTGAGTGCACCGACCCTGTCGGCCAAGGACGAGACCGCGCCCTTCCTGAAGGATATTGCCGAAGACCGTCTGCCGGTCTACGTGCCATGACCGTTCTGGTGTTCGGCGGCAATGGCCAGGTCGGCCAGGAACTGCTGCGCGCGCTGGCGCCACTAGGCAAAGTAGTCGCGACCACCCGCAGCGGGCAACTGCCCGACGGAAGTGCCTGCGAGATGGCTGATTTCGGCCAGCCCGACAGCCTGTCGGCGCTGCTGGATCGCCTGCAGCCATCGGTGGTGGTCAACGCGGCCGCCTACACGGCGGTGGACCGTGCCGAGCAGGAGGTCGATGCGGCCTTCGCCGCCAACGCGCAGGCGCCGGGCGTGATCGCGCGCTGGTGCGCGGCCCATGGCGTGCCCTTGGTGCATTACTCCACCGACTACGTGTTCGACGGCCAGGGCCGTGCGCCCTACCGCGAAGACGAGCCGACCGCGCCGCTGGGCGTCTATGGCACCAGCAAGCGCGATGGTGAGGATGCAGTGCGTTTGGCCGGTGGCCGCCACCTGATCTTCCGCACGGCGTGGGTCTATGCCTCACATGGCGCCAATTTCCTGCGCACCATGCTGCGCGTGGGATCAGAACGCGAACAGTTGCGGGTAGTGGCCGACCAGATCGGTACGCCCACTCCGGCTGCGCTGATCGCCGATGTCACCGCGCAGGCGCTGCAGCATCCGGGCCACTTGTCCGGAACCTGGCATCTGACGGCCAGTGGCCAGACCAGCTGGCATGGGTTTGCCGAGGCGATCTTCGCCGAAGCGCTGGCTAACGGTGTGCTGGCGAAGGTGCCGGCCGTCGAGGCGATTCCCAGTTCCGAGTATCCGACGCCGGCCAAGCGCCCGGCCTGGTCGGTGCTGGACAACCGCAAGCTGCAGCAGGATTTCGGCATCGTGCTGCCGGCATGGCAGGACGGGTTGAAGCGGGTGATGGCGGAGATTGCCTGACCGGGTAGGCGACCACCGTTGGTGGTCGCGTGGATCCACAGTGTGCCGACCAACGGTCGGCACTCGCTGCAGGGTGTCGCGTCAACTGCGCCCGTAGGTATCCTCGAAGCGCACGATGTCATCCTCGCCCAGGTAGCTGCCCGACTGTACTTCGATCAGTTCCAGCGGCAGTTTTCCGGGGTTGCGCAGGCGGTGGGTCACGCCCAGCGGGATGTAGGTGCTCTGGTTCTCGCTGAGCAGGATCACTTCGTCGCCGCGGGTCACTTCTGCGGTGCCGCTGACCACGATCCAGTGTTCGGCGCGATGGTGATGCATCTGCAGGCTGAGCGTGCCGCCGGGCTTGACCGTGATGCGCTTGACCTGGAAACGCTCGCCGTTATCGATTGAATCGTAGGCGCCCCACGGGCGGTAGACCTTGCGATGCCAGGCGGCCTCGCTGCGGCCTTCGGCCTTCAGTTGGGCGACAACGGTCTTGACCTCCTGCATGCGGTCTGCCTTGCCGACCAGCACCGCGTCGTCGGTCTCGACGACGATCACGTCATCCAGGCCGACCAGTGCCACCAGGCGCTGTGCATAGGCATAGGTGTTGCGGCAGTCGATGGCGATCACATCGCCCTGGTGGGCGTTGCCGTCGCCGTCCTGCTGCGAGACATCGCGCAGCGCCGTCCACGAGCCGACATCGTTCCAGCCGGCGTCCAGCGGAATCACCACGGCGTCTGCGGTTTTTTCCATCACCGCGTAGTCGATGGAGTCGGAAGGAACCGCAGCGAAGGCGTCCTTGTCCAGACGGGTGAAATCCGAATCGCGACGGGCCTGCTGCCAGGCCTGGCGGCTGCCGGCCAGCATGTCGGGCTGGAAGTGCTCCAGTTCCTGCAGGTAGCGCGAGGCCTTGAACAGGAACATGCCGCTGTTCCAGTAATACTGGCCGCTGCTGACGTAACCGGTGGCGGTCTCAAGGTCGGGCTTTTCGACAAAGCGCTCGACCGCACGCAGGCCCTGTCCATCGGCGGCCTTGATATAGCCGTAGCCGGTTTCCGGACCGGTCGGCACGATGCCGAAGGTCACCAGCTTGCCGGCCTCGGCAGCGCCGGCTGCAGCCTGCACGACTGCGCGGAACGCGGCAGCATCGGTGATCACATGGTCCGAGGGCAGCACCAGCAGCAGCGCATCGGCGCCGTCGCGGGTGGCCTCCAGGGCTGCGACCGCGATCGCCGGTGCCGTATTGCGGCCCACCGGCTCCAGGATGATGGCAGCCGGCTCGGCGCCGACCTGCTGCAGCTGCTCGGCAGCAACGAAGCGATGCTCCTCGTTGGCGATCACCAGCGGGCCGTGCGTGGCGATGGCGGCGACGCGCTGCCAGGTGGCCTGCAGCATCGTCTGTTCGCCTGCCAGCGGCAGGAACTGCTTCGGATACGCCTCGCGCGACAGCGGCCACAGGCGAGTGCCGGAACCACCGGAGAGGATGACGGGCTGGATGTTGCTCATGGTCTTCCTTGATTACTGCTGGATAAGGCGGGAAATCTCGTCGGTACGCGCCTGCATCAGCGATGCATCGCCGCGCGATTCGACATTCAGGCGCAGCAGCGGCTCGGTGTTGGAGCTGCGCAGGTTGAAGCGCCAGTCGCCGAAGTCGGCACTGATGCCGTCGGTGTGGTCCAGTACCGGCGCTTGCGCCGCGAAGTGCGCCATGACGCGGGCCACAGCGGCCTTGGCATCGGCCACCTTGAAGTTGATCTCGCCACTGCACGGATAGGCCGCCATGCGGTCTTCGACCCAGTCGGCCAGCGAGCGGCCGCTTTCGGAAATCAGCTGGGCGATCAGCAGCCACGGGATCATGCCGGAGTCGGCATAGGCGAATTCGCGGAAGTAGTGGTGGGCGCTCATCTCACCGCCGTACACCGCATCCTCGGCGCGCATCTTTTCCTTGATGAAGGCATGGCCGCTCTTGCACAGCACCGGTACGCCGCCCGCCTGCTCCACCATCTCCACGGTGTTCCAGACCAGGCGCGGGTCATGCACGACCTTGCCGCCGGGATTGCGCGCGAGGATGGCCTTGGCCAGCAGGCCGACCAGGTAATAGCCCTCGATGAAGCGGCCGGTGTGATCGAAGAAGAAGCAGCGATCAAAGTCGCCGTCCCAGGCGATGCCGAAGTCAGCACCGTGCTCGCGCACGGCGTCGGCAGTGGCGGCACGGTTTTCCGGCAGCAGCGGGTTGGGAATGCCGTTGGGGAAGTTGCCGTCGGGTTCGTGGCAGATGCGGATGAACTCGAACGGCAGGTGCGGTGCCAGCAGGTCGACGATGGCGCCCGCGCCGCCGTTGCCGGCATTCACCACCAGCTTCAGCGGCGTGAGCTTGCTGGCATCGACATAGCTGAGCAGGTGCTGGATGTAGGCGCTCTTGTCATGCTGGGCGGTCTGCCCGGCGCGCGGCGGCTGGGCCTCGGACGTATCGACGGCGACCGCGTCGGAAATCGCGAACAGGCCGGTATCGGAGCTGATCGGACGGGCATTCTCCTTGACCAGCTTCATCCCGTTGTAGTCCATCGGGTTGTGGCTGGCGGTCACCATCACGCCGCCGGCCGCACCGAGGTGATCGGTCTGGAAGTAGACCTCTTCGGTACCGCACAGGCCGATATCGATCACCTCGCGGCCGGTACCACGCAGGCCTGCGGCCAGCGCATCCTGCAGCGCCGGGCTGGTCAGGCGCACATCGTGGCCGAGGACCACCGGGCCGGGAGCGAGCTGCGCGGCCAGGGCGACGCCGATGCGGCGGGCCAGGTCATCGTTCAGTTCTTCCGGCACACGGCCGCGGATATCGTAGGCCTTGAAGGCGGGCAGGGGCATCGATCAGATCCTTTGTGAGCTCAGCCCCCAATTGTAGTCCCAGTCCCGTATGGGAATCGTTTCCATCGGGGAACGCCACCTGACTGGCGTTCGGGGGTCAGGCTCGCGTCGACCGTTTGCCCGCTTTACGGGAACGTTTGCCGGGCACGCCCGGCAACGGCGCCAGCAGCGCCTGCACGTCTTCCTCGCTGAAGCGTGGCCCCGCAGCGCCGCCGCCTTCGAGAATCGAGTCGGCCAGCGTGGCCTTGCGTTCCTGCAGCTCGGCGATCCGTTCTTCAATGCTGCCTGCGGCGATCAGCCGGTAAACGAACACCGGCTGCTGCTGGCCGATGCGATGGGCGCGGTCACTGGCCTGGTTTTCGGCCGCCGGGTTCCACCAGGGGTCGAAGTGGATGACGGTGTCGGCGGCGGTCAGGTTCAACCCGACGCCACCTGCCTTCAGGCTGATCAGGAACACCGGCACCTCGCCCTGCATGAAGCGCTGCACCGGCGTAGCCCGGTCCTGGGTGTCGCCGGTCAGGGTCACATAGGCCAGCCCGAGCTCCTCCAGCGCCTGCGCGATCAGTGCCAGCATGCCGGTGAACTGCGAGAACACCAGGACCCGCCGGCCTTCCTCGACCATCGACGGCAGCATGTCGCGCAGCAGCTCCAGCTTGGCCGAGCCGGCATTGCGTGCCGGGGCGTCGCCCGGCAGCAGGCGCGGATCGCAGCAGACCTGGCGCAGCTTCAGCAGGGCATCCAGCACCACGATATGGCTGCGCGCCAGCCCGCTGCCGCTGATGGCCTCGCGCACCTGCTTTTCCATCGCTGCACGCACGGTTTCATAGAGATCACGCTGGCCGCCTTCCATGTCCACCGCGCGGGTAATGAGGGTCTTGGGCGGAAGCTCTGACGCGACCTGGTCCTTGCGCCGGCGCAGGATGAAGGGACGCAGGCGCTGCGCCAGCAACGTGGCGCGACGGTGGTCGCTGCCACGTTCGATCGGATGGCGCCAATGCTGGTTGAACTGCTTCTCGCTGCCGAGCAGGCCGGGCAGCAGGAAGTCGAACTGCGTCCACAGCTCGCCCAGATGGTTCTCCAGTGGCGTGCCGGTCAGGCACAGGCGATGGCGGGCCTGCAGCGTGCGCAGGGTGATGGCCGCGCGAGACTTCGGATTCTTCACCTGCTGGGCTTCATCCAGAATCAGCAGATGGTAGGCATGTGCCTGCAGCGCCTGCTCGTCGCGCCACAGCAGGGGATACGTGGTCAGCACAAGATCATGCTCGGGAATCGCCTCGAACAGTGCTTCGCGCGTCGGTCCGTGCAGGGTCAGCACCCGCAGGCCAGGGGTGAAGCGTGCGGCTTCGCTCTGCCAGTTGTGCAGCAGCGAGGTCGGCACCACCAGCAGCGCCGGCTGGTCCAGGCGGCCACTTTCCTTTTCGACCAGCAGATGCGCCAGCGTCTGCAGGGTCTTGCCCAGCCCCATGTCATCGGCCAGCACGCCGCCCAGACCCTGCTGGCGCAGGTACTGCAGCCACGACAGGCCTTCACGCTGATAGGGACGCAGCGTCGCCACCAGCCCCGCCGGTGGCGGCACTTCACCCAGTGCGGGTGCCTGCATCAGGCGCTGCACCAGCGCCTGGGTATCCTTGCGCCCCCGGAACTGCAGGCGCGCCGTGTCTCGCAGCGCCTGCAGGCGACCACGGTCAAGCGCTGACAAGCGCAGCGGCGCGCCACGCTGGGTGAACAGGTCCGCCAGCAGGGCCATGATCGGCTTCAGTCGCGCGGCCCGCAGTGCCAGGCGGGTGTTGTCGCCTGCCATCAACAGGATGTTCTCGTCATCGCCGATGGCGTCCAGCTGGCCACGCATCCAGCGGGGATCGGACTGCAGCACCTGCTGCAGCAGCGGAACCATCGACACGTTGCGGCCTTCCACCTGGATGTCCAGGCCCAGGTTGAACCAGCCCGCATCCGCCGGGTCGGTCTGGATGTCCAGGCCGATCTCATCCACCCGGGTGATGCGATGGCGGAAATCGTCGTCCGTCTCCACTTTCCAGCCCAGGGCTTCCAGACGCGGCAGGTCGTCCAGCAGGAACCGTGTCCAGTCATGGGTGCGCAGCTGGAACTGCGGGCCTGCGCCCTCCAATGGCGCCCGCGGGGCCGTGTCGCGATGCAGTCCCACCGTGCGCAGCTCGGCCTCGCGCCGTGACTCCTCAACCAGGTCGCGGGGCAGCAGGGCGAGCTGGCCCTCCGGATCGTGTGCGAACAGGCTCGGATCATCCAGGAACCGCACGTGCTCGTCGTATTCGAAGGCCACGGTCGCGATATCGGCCCACTGCGACGGGTCGCGGCGGCCGAGCCACGGCGGACGGAACTCGACCGTGTGCAGGCGCAGCACGGGAATCATCGAGGCGATCTGCAGGGTGGGCAGCGTGTCGCTTGCACCGGGGCGCGGCAGCGCAGGGTCGATCTGCTGCAGCAGTTGCGCCACGATCGGTTCCTCATCGGGGAGCAGGTGGGGAAGGGCGAGGAACGCGTCCGCGTCCTCCGGCTTGACGTCCAGCAGGAGAAGCCCGACTTCACCGGAGACCGGATCCAGGTAACCGGCACTGGATCCCAGTACGAGGCCTTCCGCATCGCCCTCCACGCTCAGTGTCGGCGCCAGCAGCAACCTGCCGTGAGTCGTCTCTGCGCTCCATCCCAACGTACCGCGACGTGGTGTGCCGGGCCTGGCCGGCACGCGGTCATGCATGCCACATGACACCCAGCCATGCTCGCTGGACACGATCGACTGCAGGATCGTGCCGATGTCGAACCGTTCCGGCGGTTTCACGGACTGATGCAGGGCCCACAGCTGCGCCACCGCGGCCAAGTCGGCCTGCGTCAGGTAGCCAGGTGGTTCCAGCAACAGCTGAGGGGTGATTTCCTGCCATTTGCCGAACTCGATCGTGCCGTCGAGGGCGTACTTGACGCGACGGAGCAGGATGGAAGGCCGGTGATTGAACGTGGACAGCTCGAAGATGATGCCGTTTCTACGTGACCGGGGAGGCTGGGCTCTGGCGGCCTGCCAGCGTGACAGCTGTTCCAGCAGTTCGCGGCGTGGTGACTGGACCGGATCGTGCTCCAACGCTGGATCGTCATCGCCCAGGTCTGCCGCGTCCAGCATATGCGCGACCAGCACGGCCGCCACGTGCTTGCAGTGATGGCCGACAGGGCACGAGCATTCACTACGCAGGCGGCTGCGGGGATGGCGCAGGCTGGCTTCCAGATCGATTTCCACCCGGTAGGGGTATCTGGCCGAGCCTTTCACTTCGGCGATGAGCATTCCACTGGTCAGATGCATGTTGCGGACACCGGACAGGCAACGTTCGCTCTTTTCCAGTGTCCACGCGTCCATCCAGCGGAGCAGGTCTTCTTCGGTGTAGATCTGGGCCAT

Protein sequences of DBSCAN-SWA_1

>NZ_CP047310|572252:584892|575231_576287_+|WP_159359771.1|DBSCAN-SWA
MPTWLVTGGAGFIGGNFVLEAVARGVKVINLDVLTYAGNLRTLSSLDGNPNHLFVQGDIGDQALVANLLAEHRPDAVVNFAAESHVDRSIDGPGAFIQTNVVGTLGLLEAVRDYWKALPAEQGAAFRFLHVSTDEVYGTLGETGKFSETTPYAPNSPYSASKAASDHLVRAFHHTYGLPVLTTNCSNNYGPYHFPEKLIPLVIAKALAGEPLPVYGDGKQVRDWLFVSDHCEAIRTVLAKGQVGETYNVGGNSEKQNIEVVQAICALLDQRRPRADGQPRSSQITYVTDRPGHDRRYAIDASKLKNDLGWEPAYTFEQGITFTVDWYLDNQEWINGVLDGSYRLQRIGTAA
>NZ_CP047310|572252:584892|577739_578633_+|WP_049480751.1|DBSCAN-SWA
MTVLVFGGNGQVGQELLRALAPLGKVVATTRSGQLPDGSACEMADFGQPDSLSALLDRLQPSVVVNAAAYTAVDRAEQEVDAAFAANAQAPGVIARWCAAHGVPLVHYSTDYVFDGQGRAPYREDEPTAPLGVYGTSKRDGEDAVRLAGGRHLIFRTAWVYASHGANFLRTMLRVGSEREQLRVVADQIGTPTPAALIADVTAQALQHPGHLSGTWHLTASGQTSWHGFAEAIFAEALANGVLAKVPAVEAIPSSEYPTPAKRPAWSVLDNRKLQQDFGIVLPAWQDGLKRVMAEIA
>NZ_CP047310|572252:584892|578714_580118_-|WP_159359772.1|DBSCAN-SWA
MSNIQPVILSGGSGTRLWPLSREAYPKQFLPLAGEQTMLQATWQRVAAIATHGPLVIANEEHRFVAAEQLQQVGAEPAAIILEPVGRNTAPAIAVAALEATRDGADALLLVLPSDHVITDAAAFRAVVQAAAGAAEAGKLVTFGIVPTGPETGYGYIKAADGQGLRAVERFVEKPDLETATGYVSSGQYYWNSGMFLFKASRYLQELEHFQPDMLAGSRQAWQQARRDSDFTRLDKDAFAAVPSDSIDYAVMEKTADAVVIPLDAGWNDVGSWTALRDVSQQDGDGNAHQGDVIAIDCRNTYAYAQRLVALVGLDDVIVVETDDAVLVGKADRMQEVKTVVAQLKAEGRSEAAWHRKVYRPWGAYDSIDNGERFQVKRITVKPGGTLSLQMHHHRAEHWIVVSGTAEVTRGDEVILLSENQSTYIPLGVTHRLRNPGKLPLELIEVQSGSYLGEDDIVRFEDTYGRS
>NZ_CP047310|572252:584892|576301_577189_+|WP_049480755.1|DBSCAN-SWA
MTQRKGIILAGGSGTRLYPITKGVSKQLLPVYDKPMIYYPLSVLMLAGIREVLIINTPHEQALFQQLLGDGSQWGMDIQYAVQPSPDGLAQAYLIGRDFVAGKPSCLVLGDNIFHGHGLREVLKRADERVHGSTVFGYWVNDPERYGVAEFDQSGKVIDLVEKPEKPRSNYAVTGLYFYDGKASDYAAELKPSPRGELEITDLNKRYLEEGNLHLEALGRGYAWLDTGTHQSLLEASNFIETIQTRQGLQVCCPEEIAFGKGWITAEQLEALAAPLIKNGYGQYLHKLALRGVVP
>NZ_CP047310|572252:584892|574222_574969_-|WP_159359770.1|DBSCAN-SWA
MKILVAYKRVVDYNVRIQVKPDGSGVVTDGVKLSPNPFDEIALEEALRLRDKGIASEVVVATIAPADAQAHLRNGLAMGANRAIHVVTDQAIQPLTASRTLLKLIEKEQPDLVILGKQAIDDDANQTGQMLATLWGRPQATFASKLEIADGKATVTREVDAGLETLEVELPAVVTTDLRLNEPRFIKLPDIMKAKAKPLETLQLADLGVEAADTFKTTQYAAPSKRSKGVMVKDAAELVAALKQKGLL
>NZ_CP047310|572252:584892|580130_581477_-|WP_159359773.1|DBSCAN-SWA
MPLPAFKAYDIRGRVPEELNDDLARRIGVALAAQLAPGPVVLGHDVRLTSPALQDALAAGLRGTGREVIDIGLCGTEEVYFQTDHLGAAGGVMVTASHNPMDYNGMKLVKENARPISSDTGLFAISDAVAVDTSEAQPPRAGQTAQHDKSAYIQHLLSYVDASKLTPLKLVVNAGNGGAGAIVDLLAPHLPFEFIRICHEPDGNFPNGIPNPLLPENRAATADAVREHGADFGIAWDGDFDRCFFFDHTGRFIEGYYLVGLLAKAILARNPGGKVVHDPRLVWNTVEMVEQAGGVPVLCKSGHAFIKEKMRAEDAVYGGEMSAHHYFREFAYADSGMIPWLLIAQLISESGRSLADWVEDRMAAYPCSGEINFKVADAKAAVARVMAHFAAQAPVLDHTDGISADFGDWRFNLRSSNTEPLLRLNVESRGDASLMQARTDEISRLIQQ
>NZ_CP047310|572252:584892|581574_584892_-|WP_159360778.1|DBSCAN-SWA
MAQIYTEEDLLRWMDAWTLEKSERCLSGVRNMHLTSGMLIAEVKGSARYPYRVEIDLEASLRHPRSRLRSECSCPVGHHCKHVAAVLVAHMLDAADLGDDDPALEHDPVQSPRRELLEQLSRWQAARAQPPRSRRNGIIFELSTFNHRPSILLRRVKYALDGTIEFGKWQEITPQLLLEPPGYLTQADLAAVAQLWALHQSVKPPERFDIGTILQSIVSSEHGWVSCGMHDRVPARPGTPRRGTLGWSAETTHGRLLLAPTLSVEGDAEGLVLGSSAGYLDPVSGEVGLLLLDVKPEDADAFLALPHLLPDEEPIVAQLLQQIDPALPRPGASDTLPTLQIASMIPVLRLHTVEFRPPWLGRRDPSQWADIATVAFEYDEHVRFLDDPSLFAHDPEGQLALLPRDLVEESRREAELRTVGLHRDTAPRAPLEGAGPQFQLRTHDWTRFLLDDLPRLEALGWKVETDDDFRHRITRVDEIGLDIQTDPADAGWFNLGLDIQVEGRNVSMVPLLQQVLQSDPRWMRGQLDAIGDDENILLMAGDNTRLALRAARLKPIMALLADLFTQRGAPLRLSALDRGRLQALRDTARLQFRGRKDTQALVQRLMQAPALGEVPPPAGLVATLRPYQREGLSWLQYLRQQGLGGVLADDMGLGKTLQTLAHLLVEKESGRLDQPALLVVPTSLLHNWQSEAARFTPGLRVLTLHGPTREALFEAIPEHDLVLTTYPLLWRDEQALQAHAYHLLILDEAQQVKNPKSRAAITLRTLQARHRLCLTGTPLENHLGELWTQFDFLLPGLLGSEKQFNQHWRHPIERGSDHRRATLLAQRLRPFILRRRKDQVASELPPKTLITRAVDMEGGQRDLYETVRAAMEKQVREAISGSGLARSHIVVLDALLKLRQVCCDPRLLPGDAPARNAGSAKLELLRDMLPSMVEEGRRVLVFSQFTGMLALIAQALEELGLAYVTLTGDTQDRATPVQRFMQGEVPVFLISLKAGGVGLNLTAADTVIHFDPWWNPAAENQASDRAHRIGQQQPVFVYRLIAAGSIEERIAELQERKATLADSILEGGGAAGPRFSEEDVQALLAPLPGVPGKRSRKAGKRSTRA
>NZ_CP047310|572252:584892|572252_573248_-|WP_159360777.1|DBSCAN-SWA
MRAEAGNQNPPDSGPTPDVSVVVPVYGCEGCLEQLSERVAGAISGMGLTHELILVDDQGPDQSWQRICELGKLSSRVRGLRLSRNFGQHAAISAGLQYAQGSRVIVMDCDLQDVPEEIPSLLAGLEGDNEIVLGQRVERQDTWLKRSGSSAFYKALGWLTDTDYDPSTANFGAYSRKAVDAMNAMPETDRFLPLMARWTGFKTLRVPVSHGRRTEGKSGYTLRKLLQMATRIALSFSDKPLRLVMTAAFALAAIGAGIALLAVYRYWAGDIRVAGFTSILASIWLVGSFIMGSLGVVGLYIGRIHSESKRRPQFIIWQDTWQGTHSNVSED
>NZ_CP047310|572252:584892|573284_574223_-|WP_159359769.1|DBSCAN-SWA
MSKILVIAEHHDGKLNAATAKTVSAAAAISGASIDVLVLAADPAAVAAEAAKIAGVAKVLTVANAANAQAIAQVLAPQIAQLAKGYTHVFGPSTTFGKDLMPCVAALLGVNQVSDLMSVEGSHTFKRPIYAGNAIITVETPADQIVVATVRAASWPEAAQGGSAAVEAASVDAALPTHTRFVGLAAGASDRPDLQSAKRVVSGGRGVGSEENFKVIFQLADKLGAAVGASRAAVDAGYVPSDLQVGQTGKIIAPELYVAVGISGAIQHLTGIKDAGTIVAINKDADSPIFEIADIGLVGDLFAILPELEAAL
>NZ_CP047310|572252:584892|577185_577743_+|WP_049480754.1|DBSCAN-SWA
MKVIETKLPGCVVIEPAVFGDARGYFFETWNAERFAALGLPDRFVQSNVSTSAQGVLRGLHYQWPRPQGKLVSVLEGEVYDVAVDIRRGSPTFGQWEAVVLSAENKKQFWIPEGFAHGFAVLSERAVFSYLCTEVYLKDFDAGVRWNDADIAVDWPVSAPTLSAKDETAPFLKDIAEDRLPVYVP

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_159360777.1|572252_573248_-	glycosyltransferase	F1C5B0	Cronobacter_phage	8.2e-29	30.3
WP_159359769.1|573284_574223_-	electron transfer flavoprotein subunit alpha/FixB family protein	NA	NA	NA	NA
WP_159359770.1|574222_574969_-	EtfB protein	NA	NA	NA	NA
WP_159359771.1|575231_576287_+	dTDP-glucose 4,6-dehydratase	I7HTA3	Enterobacteria_phage	1.4e-79	46.8
WP_049480755.1|576301_577189_+	glucose-1-phosphate thymidylyltransferase RfbA	I7I009	Enterobacteria_phage	3.7e-97	58.5
WP_049480754.1|577185_577743_+	dTDP-4-dehydrorhamnose 3,5-epimerase	I7HJC4	Enterobacteria_phage	2.1e-45	51.1
WP_049480751.1|577739_578633_+	dTDP-4-dehydrorhamnose reductase	A0A291LA50	Escherichia_phage	1.8e-27	37.5
WP_159359772.1|578714_580118_-	mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase	A0A1V0SH58	Hokovirus	2.1e-46	28.7
WP_159359773.1|580130_581477_-	phosphomannomutase	A0A127AWJ1	Bacillus_phage	2.7e-30	26.6
WP_159360778.1|581574_584892_-	helicase	Q9YNZ9	Choristoneura_fumiferana_nuclear_polyhedrosis_virus	1.4e-48	30.5

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP047310|2147610:2154774|DBSCAN-SWA
GTCATTGAGAGCGTTGGCTTTCGTGGCCTATCAAGGACTGAATGGAGCCGCCTTTGAAGAGGAAGAGATCATTGTCGCGGGGGTCGGCTTGGTCTGCGGCTGGATCGCTTGGGTCATGTACAAGACCCTGATCGGACGATGGAGAAAGCCGTAGCTGCCAGGCCGCGAGGGGCACGCTGGGGAGGCTGGCTTCTTGGCTTGGCATGGCAAGGTGATTGAGGCGAACGGTACGCCAGCGCCCCTCGGGGATGCTTTGAACATAATATACAGAATGGGTCAGTAGACCCGAGCTAACCGCCTGATTTTGGGCGGTTTTTGCGTTTCCGAGGCTCGGCAACGACAGCGCCACCAGCGCGACGACCGCAGCCGCCGCGCTCATTCGGTCCAGCATCAGCCGCCATAGCGCACGCTCGGTTGCAGAGGTCGCCCGCTCGGCGTGGATCATCGCGATCCACGTGGGGCCATCCAGTTTTGCCAGTGCGCAGATCTGCGCAATTCGCTCATCAGCCAGCGGCGTGTCGCCTTTCCGCCACCTGGACACAAGCGAACGGGTCACCGTCAGCCTTTCGGCCAAAGCCATGTCTGACGCGAGATTCAAGCGGATTTTCACGTTGTCAAGTAGTTCGTTGACGGCGGTCATGGCGGCTCCAGTTGATCGATCAGTTGACACGTGTTTCGTGATCAGTTTACATGCGCCACGTTGAGTGATCACTCAACACCCGCCACCGGCACCCCAAGGCCGCTGGCGGGTTCTCTTGGGGCTTGGGGTAGGGGACAGGGATGATCGATCCGCTCATTACCTTCGTGCTGCTGGCGGCCATCGTGGCCGTATCCATTGGCATCGCCAAACTCGTTTCGTGGTGCCTCGACCGGCGTGGGGAGTCCGCCCGTCGCAGCGCACACGAAGCGGCCTTCGTCGCCCGGGTACGCGCCGAACTGGCCGCAACCGATTGGACCCCGGATCGCGAAACGCTGTATCAGGCCGAAATCGCCGCCACCAAGCGCGGTGATCTTCTTGCTGCCGCTCGCTATGCCGAAGAGCAGGAGCGCGCCGCATGAGTACGTTTCCCACTTTCGCCGAACTGGCGGAGTTCGATATGGGTCTTGCCGGGTGCGCCGCTCTCATCGCCGTTTGGCTGGGAGTGGCATTGCTCTCCATCGTGATCGAGCAGGCATGGCTGGGGCTTCGTCGCCTGTGGAAGCTCGGCAAGGACCGCGCCAATGGTCGGTGATCGCGCGGTGCTGGCCGGGTCGGGACTCCCCTCGTCTAACAGGGGAGTCAGTGAATTCAGGAACGCCGATGGAACCCTGACGGTCGGCATTGACTGGTTCTCCGCTTCCATTGATCTGCGCGCAGCGCTGGACGAACTCGCGTTCCGTGATGGCGACAGCTTTGAAGAGGTCCGCCAGTGGATTGAGTTCTCCCCGGAGAACGCACGCATCGCGGCCTTGCAGGTGTTCTGCTGGTTCTTCGCCGGCCTTGGCCTTGAACTGGATGAGGTAGCGGGCGGCGGTCGCTTCTACACGTGGCGAGTCAAGATCATCGACGCGGCCAAGAAGTTCGTCGGCATGATCGAACTGGGCGGCGAAGAGTGCCGACGCGCGGATGGCACGTATACCGCCCGCATCGAGCTAACCGGTGATGGATGCAAGGCGATAGGCGCAGCGCGCTGCGGCCATGCGCAGCGGTGGCTGGAGCTTCGAGCGAAGCTCGAAAGCTGCGCCGGGAGGATCACCCGTGTCGATGTGTGCGCCGATGACCTGGTGGGCGACTACCCATTGCGCATGGCACAGAAGTGGTACGAGGAAGGCGAGTTCAACAATCGCGGTCAGCGCCCCAAGGCACAGCTGGTGGACGACTACGACAGCGGTGACGGCAAGACGTTCTATGTCGGCGGCAAGAAGTCGGAAAAGCAGCTGCGCGTCTACGAGAAGGGCAGGGAGCAGGGCGACAAGAGTTCGCCGTGGGTGCGCTATGAGGCGCAGTTCCGCAATTCCAACCGCAAGGAACTGCCACTCGACATTCTGCGTGATCCGGCGGCCTACCTGCTCGGCGCCTATCCAGTCCTGTCCTTTCTGCGCTGCGTTGCCACGCGCATCGAAATCTCAAAAGCCGCCGTTGAAGCGACGTGGAAGAGCGTTCGCCGTCACATCCGCCGCCAGTACGGCGCGGCCCTCAATTTCATCGCCAAGAACTGCCCTGACGATCAGGCGTTGCGGGCGGTAATCGAATCCTGCACTTCGCCATCGCTGCCGAAGTGGGTCACAGGTGACACAGCAGCGCACTGGCCCGAAATCGCGGCCGTACAGCCAACCTCAAAGGGGTAACAGCACATGAGCATCAAGGTCACTGTCCTGAAGAACGAAATCGACGAACGCGGCGGCAGCTTCAAGAATGACGCTGGCGAGAACGTCGAGTACACCACCCGCAAGCAGAAGGCGAAGCTTGAAACCGGTGGTTTTGCGTATCCGTTCGACGTGCGCCTGGACAAGGGCCAGCCGGGCTATCCCGAAGGCGAGTACGAGCTCGACGTGGAGTCCATGTTGCAGGTCAACAAGGGCGTCGCATCGCTGAGCAAGTTCACCGTCCTGCGCATGGTGCCGAAGGGCGCACCTCGCGCGGCTGCTCAGGCCTAAGTCATGGCCGTGTGCGTGTCTCTGACAGCTGAGGGGACGCTTGTACCCACCGGGGAGCCTGCATCGCAGTGTGGTGGGTATGTGCTTGTGTCGGCGGCAGAACACGCACAGGCCTCAATCCTCATCGATCTATTCCAGTGGCCCGAACCGGAAGTGGCCGCTGGTTGGTTCTCGGGGGTGTTCACGCTGGTGCTCGCACTGAACGTGCTGGGCTACATCGTGGGCGCCGTCGTGAAGTCGGTCAGTACAGAGCGGGATTGACCACCCCATCTAACGCGCACAACGCGCACAACAAAGGAGCAGTGCAATGGACTTCAGCGACATTCTGACCGGCCTCGCAGCCGCCAGCGCAGTCAGCGCAATCATCAGCGCAGGTGCCATCAAGGCATCCCCGGGCTTCGCCCGCTGGGCGACCAACAAGGTCGCGACCTTCTTCCGCTGATCGCGGAAGAATCGTGACGGGGAGGGGCCGGGAAACCGGCCCCGATTCCTATGCAGACGCAGCCCGATGACTTCAACACCGACGAATACCAGGACGACTGGTGTCCCGAGTGCGGCGGTGATGACGTGATCGCGTTGGACGACGGCGAACTATGGTGCACGGAGTGCCGCGCCGTCATCGATTACTAGGGGCTGATGATGGATTTCAGTGGGGTTTTTCTCGGGCTGTCCGTTGCTCAGGCTGTCGCTGCGATCGTTGCAGCGGGGACGCTCATGGCGCTTCCGTGGTTTGGCCGTTGGTGCGTTGACAAGATCGCGGGCTTCTTTGAGGACCGGGAGGATCAGGACGCCGACGAGCATGCCGACGAAGAGGCGGGCGAGGTTGAGGAGGCCGTCTGTGGCGACACCGGCCATGACTACGACGGCGGGGAGTGCATCTTCTGCGGCCAATCAGAGGGGGAGGACTGACGATGCTGGTTTGCATGGTTTTCGCATTCATAGGCGGCCTTGCCGGTCATGCGGTCGCCCTTGCATTTAATGAGGCGAGCCAGTGAGAAGTTCGCTATTAGTTGTGCTTCTCACCATTAGCGGCGTAGCGGCACACAGTGCCCATGCGGCTACTCAGTGTCTGGACAATGAGAACTGCGATAAGGGGCAGGCTCGGGAGTCGTGTGAAACGTTTCCCGTGAACATCGCCGGCAATAGCACAGTTGTCTCATACACCAGGCGGCAGTGCATTGCTGTTGACAATGGCACGAGGGGCTACTTTCTATCCCAGTACTTTGGCAAACAGGCCAACGGGGTTGAGGCAGGACCATTCAATTACTTAAGGCACTACTGGGCTTCTCTTTGTACGGCGCGGCCGGAGGAGACCGGCTGGAAGGGTGGCGGCAGCACTGGCCTAGATAGCGTGTGCAGCAACGGTTGCACATATAGCGGCTCGCTCTATGCCCAGTCGCCGACTGGTCGCCTTTTCACCCCTACCGGTGCCACGTGCACCACAGATGACCACCCTGCACCCACCACGCCCGACCCCGGTGAGGGAGGAGGGGATGGCGGTGGTACTGGCCCGGGTGACGGCGGTGGTGACGGCGGCGGTGACGGCGGCGGTGATGGGGGTGGCGATGGCGGCGGTGACGGTGGAGGCGGTGATGGCGGCGGTGGCACCGGGCCGGGTGATGGTGATGGTGATGGTGATGGTGATGGCGACTGCAAAGACCCGGACGGCTGTGCGGGACCCGGGCCGGGACCTGGTCCGGGCGAGGGCGGTGGTAGTGACGGAGGGGCGCCGGGACCTACGACAGGGCGCCTCTACAAGAAGTCCGGCAAGACGGTCCAACAGGTGATAGCGGAGTTCAAGACGGCCATTGAAGGCGCCCCGATCTTGTCGAAGGTCAAAGGCTTCTTCGGCAGCTGCACAGGCGGTGGCAGTTGCCCGACGGCAACATGGGACGGTGGGCAGTACGCGGGCAAGTTTGACCTGGCCTCGCTGTGCTCTGGCCCACTGCTACAGCTATTCCAGTACGCCGGATTCGTCTTCCTTGCAGGCATGGGCATCGTGGCGCTGAGGTGGGCACTGCTATGAAGCGTAATCATCTGATCGTGCTGGCTGTTGCGCTGATTGTGCTCGTGCTGTCAGCTTCGTGGGCATATGCCGATGGGGTAGGGCCGGTCACCGCCCTTACCACGTGGGCAAAGGAACAGATCACGTCGTTGTGGGCGGACTTCTCCGACTTCATGACGGATCTGCAGACCGACTTCATCGAGTTGGTGTTGTCGTTCGTCAAGGCCATCGTGTACCTGATTCCAGCGCCTGATTTCCTATCGCAAATCAGCTTCTGCGCAATGCTCAACGCTGCGGGGCCGTGGACCGCCTTCATCGTTGCCCAGTTGCGCGTCGGTGAGGCTATCGCTGTGTTGACGGCTGCACTTGTATTCCGCCTTGTGCGGGTGTTCCTCACTCTCTTCCAGTGGACGTAACGAAATGATCTTCGGCCATGAGGGGTTGCCGCGCAGCGGCAAGAGCTACGAGGCGGTGCTGCACCATATCCTGCCCGCGCTCCGCGCAAAGCGGCATGTGTACGTGCGCCTAAACGGGGTAGGGGAGAGCCTCGACAAGATCGCCGCGCACCTGGGCATGCCTGAAGAAGAGGTGCGCGAGCTGGTGCACGTGATGGGCGACAGGGAAGTGGTTGATTGGTGCGTATGCGACACCGACAACGATGGCGCCATTTCGTTTCCGCATATCGAGAAGCACGCACTGATCGTGATCGATGAGGCACACGAATACTGGCCGACCAACCGCGCCAACCTCCCCGAGCGCACTGCAAACTTCTTTGCTAAGCACGGCCATATCAGCTTGGACATGGTGATCATTTCGCAGGACTGCAAAGACCTGCACCGCCTGATCATCCGCCGCATGGCGAAGAAGAACACGTATACCAAGCTCGACGCGCTGGGGTCCGATCAGCGGTACTCGGTGCGGTTCTACGCGGCCACTGGCACCGGCAAATACGAAACGGTGGGCACAGAGGTCCGCAAGTACGATCCGGCCATCTGGGAGCTCTACCACGGCGTACAGCCGGGCATTGAGTCCAATGAGGTCTACAAGGGAAACACGCGCACTTTGTGGAAGACCCTGCGCGGCCCATCAATCGTAATGGGCCTCGCACTTGTCATTGGCGTGGTGATGTTCCTGCGGTTCTTCTTCGCAGACGGCTCAACGGGCGAGGAAAGCAAGCTCAAGGAGGTTGTCAAAACGCAGAAGGCCGCAATTCCCGCGATAGCGCACGCACCGGGTGCTCAGCCGGCCACGGTGGTCACAAAGGTTGTCGAGACGCCCAAGACGAAGGAGAAGCTTCCTGCGGGCGTTCAGTACATTCTGGACATGGCGGCCAATGCCAGGGCGAGGCACGCCGGGTGGTACGGCCAGCGCGACATCGTGGAGTTTCGCGCGTCAGGCGGCGGGCAAGTACTCGATCGATTCACCACTGAGCAGCTGTGGGCGCTGGGCTGGTCTGTCAAGCGAACCGAATTCGGCGTGTTACTGAGCGCTAAGGGGCATGAGATTATCGCCACGACTTGGCCCGTGGATCCGTTTGGCGAGCAGTCCGATGCTACGACCGCGCGCATAAGGGCTGCGGCGGGGTCGCCTGTGACGAGCGCGAGCGAGACACAGCCGACCACCGCCGCGGCGAACGGGAGCACCCTAATTGCAGTTGGGAAGCGCCCCTTGGGCACGTTCCCAGAGACGCCGCCATACCCGGCGAGCTTCTGATTTTCGCAATGGGATACCATGCCCCCGAACCTTGGGGGCGAAATGGACATTCGATCAGGCCTAGTTCTGGCTCTAGTGCTGCTGTGGGCACCTGCGCATGGGCAACAACTACGCTCGGCCACCGGTCCACAGCCACCGCCCAGGTACACGCCGCCAGCACCGAAAGCGAGCAACCTCGGCGCTGAGCCGCTGAAATGCCAGCAACACGTTGATCCGCGAATTCGGCTCTATTGCGCGGAAATTGAGCGATCCCTGATACAGGGCGAGGCGCGTCGTCAAGGGTTACCAACGCCGTCGAGCGAGATTGTTCGCATGCCAGCCTACGGGAGCGCTGAGGCAAAGCAGCTGGGTGCTGCCTGTATGGGGGGCACCGCGATGCGCCGCCTAAACAACGGCTGGGAACAGTTGCGAAATGCGAAGGGCGAATGGCTGCGCTGCCGCGAGCAATGAACCGGGGTGTAGGGGCGGCGCCCCTACGAAAACGCCTCACACGCGCTGGCGAGACCTCGGCCCCGGTACCCGCAGGACACCTGCAGCAGGATCGGCGTCGGGACCAGCCATCACCGTGGAAGACCGCTTCGCGCGGCGGTGGGCAACCTCAGCGAGGTCAACGATGCCCGCACGCCCGAATGGCCGTTTCTGACCGCCTCGGGCAATCTCCATCATCCGGCGCCATTCCTGCGCCTGTGCGGCCAGCAGGGACAGCCATGCAAGGTCCTGCGGTTCCAACTCGCGGCCTTCGGGTGTAACCAGTCGGCCACCCTTAAACGAAAAACCGGCCCAAGGGCCGGTTAGGTTGCGATCACGCAC

Protein sequences of DBSCAN-SWA_2

>NZ_CP047310|2147610:2154774|2154450_2154774_-|WP_159360143.1|DBSCAN-SWA
MRDRNLTGPWAGFSFKGGRLVTPEGRELEPQDLAWLSLLAAQAQEWRRMMEIARGGQKRPFGRAGIVDLAEVAHRRAKRSSTVMAGPDADPAAGVLRVPGPRSRQRV
>NZ_CP047310|2147610:2154774|2147610_2148249_-|WP_159360135.1|DBSCAN-SWA
MTAVNELLDNVKIRLNLASDMALAERLTVTRSLVSRWRKGDTPLADERIAQICALAKLDGPTWIAMIHAERATSATERALWRLMLDRMSAAAAVVALVALSLPSLGNAKTAQNQAVSSGLLTHSVYYVQSIPEGRWRTVRLNHLAMPSQEASLPSVPLAAWQLRLSPSSDQGLVHDPSDPAADQADPRDNDLFLFKGGSIQSLIGHESQRSQ
>NZ_CP047310|2147610:2154774|2148664_2148841_+|WP_159360137.1|DBSCAN-SWA
MSTFPTFAELAEFDMGLAGCAALIAVWLGVALLSIVIEQAWLGLRRLWKLGKDRANGR
>NZ_CP047310|2147610:2154774|2150553_2150688_+|WP_095378027.1|capsid|DBSCAN-SWA
MDFSDILTGLAAASAVSAIISAGAIKASPGFARWATNKVATFFR
>NZ_CP047310|2147610:2154774|2148830_2149937_+|WP_159360138.1|DBSCAN-SWA
MVGDRAVLAGSGLPSSNRGVSEFRNADGTLTVGIDWFSASIDLRAALDELAFRDGDSFEEVRQWIEFSPENARIAALQVFCWFFAGLGLELDEVAGGGRFYTWRVKIIDAAKKFVGMIELGGEECRRADGTYTARIELTGDGCKAIGAARCGHAQRWLELRAKLESCAGRITRVDVCADDLVGDYPLRMAQKWYEEGEFNNRGQRPKAQLVDDYDSGDGKTFYVGGKKSEKQLRVYEKGREQGDKSSPWVRYEAQFRNSNRKELPLDILRDPAAYLLGAYPVLSFLRCVATRIEISKAAVEATWKSVRRHIRRQYGAALNFIAKNCPDDQALRAVIESCTSPSLPKWVTGDTAAHWPEIAAVQPTSKG
>NZ_CP047310|2147610:2154774|2148389_2148668_+|WP_159360136.1|DBSCAN-SWA
MIDPLITFVLLAAIVAVSIGIAKLVSWCLDRRGESARRSAHEAAFVARVRAELAATDWTPDRETLYQAEIAATKRGDLLAAARYAEEQERAA
>NZ_CP047310|2147610:2154774|2151739_2152033_+|WP_159360140.1|DBSCAN-SWA
MAVVLARVTAVVTAAVTAAVMGVAMAAVTVEAVMAAVAPGRVMVMVMVMVMATAKTRTAVRDPGRDLVRARAVVVTEGRRDLRQGASTRSPARRSNR
>NZ_CP047310|2147610:2154774|2149943_2150246_+|WP_088430765.1|DBSCAN-SWA
MSIKVTVLKNEIDERGGSFKNDAGENVEYTTRKQKAKLETGGFAYPFDVRLDKGQPGYPEGEYELDVESMLQVNKGVASLSKFTVLRMVPKGAPRAAAQA
>NZ_CP047310|2147610:2154774|2150738_2150876_+|WP_159360139.1|DBSCAN-SWA
MQTQPDDFNTDEYQDDWCPECGGDDVIALDDGELWCTECRAVIDY
>NZ_CP047310|2147610:2154774|2152671_2153964_+|WP_159360142.1|DBSCAN-SWA
MIFGHEGLPRSGKSYEAVLHHILPALRAKRHVYVRLNGVGESLDKIAAHLGMPEEEVRELVHVMGDREVVDWCVCDTDNDGAISFPHIEKHALIVIDEAHEYWPTNRANLPERTANFFAKHGHISLDMVIISQDCKDLHRLIIRRMAKKNTYTKLDALGSDQRYSVRFYAATGTGKYETVGTEVRKYDPAIWELYHGVQPGIESNEVYKGNTRTLWKTLRGPSIVMGLALVIGVVMFLRFFFADGSTGEESKLKEVVKTQKAAIPAIAHAPGAQPATVVTKVVETPKTKEKLPAGVQYILDMAANARARHAGWYGQRDIVEFRASGGGQVLDRFTTEQLWALGWSVKRTEFGVLLSAKGHEIIATTWPVDPFGEQSDATTARIRAAAGSPVTSASETQPTTAAANGSTLIAVGKRPLGTFPETPPYPASF
>NZ_CP047310|2147610:2154774|2152268_2152667_+|WP_159360141.1|DBSCAN-SWA
MKRNHLIVLAVALIVLVLSASWAYADGVGPVTALTTWAKEQITSLWADFSDFMTDLQTDFIELVLSFVKAIVYLIPAPDFLSQISFCAMLNAAGPWTAFIVAQLRVGEAIAVLTAALVFRLVRVFLTLFQWT

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_159360135.1|2147610_2148249_-	hypothetical protein	S0F2J2	Stenotrophomonas_phage	1.2e-52	95.8
WP_159360136.1|2148389_2148668_+	hypothetical protein	S0F3S0	Stenotrophomonas_phage	5.3e-18	65.5
WP_159360137.1|2148664_2148841_+	hypothetical protein	NA	NA	NA	NA
WP_159360138.1|2148830_2149937_+	replication protein	S0F3I3	Stenotrophomonas_phage	6.4e-208	94.8
WP_088430765.1|2149943_2150246_+	single-stranded DNA-binding protein	B1NI78	Stenotrophomonas_phage	1.6e-44	92.8
WP_095378027.1|2150553_2150688_+|capsid	capsid protein	NA	NA	NA	NA
WP_159360139.1|2150738_2150876_+	hypothetical protein	S0F2B8	Stenotrophomonas_phage	9.8e-18	84.4
WP_159360140.1|2151739_2152033_+	hypothetical protein	NA	NA	NA	NA
WP_159360141.1|2152268_2152667_+	hypothetical protein	S0F3B3	Stenotrophomonas_phage	8.6e-62	96.2
WP_159360142.1|2152671_2153964_+	Zona occludens toxin	S0F2C3	Stenotrophomonas_phage	5.5e-251	99.5
WP_159360143.1|2154450_2154774_-	hypothetical protein	S0F2C0	Stenotrophomonas_phage	2.7e-50	92.5