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_CP045802	Paenibacillus sp. B01 chromosome, complete genome	28 crisprs	DEDDh,WYL,csa3,cas3,DinG,cas14j	5	23	7	0

1. NZ_CP045802

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP045802_1

• CRISPR_ID: NZ_CP045802_1
• CRISPR_location: 80411-80585
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP045802_1

Consensus_repeat	Method
GGACGGACATCTGGTGGATGACGGACGTTAGGGACGGACATGT	PILER-CR

spacers of NZ_CP045802_1

>1.1|80454|42|NZ_CP045802|PILER-CR
CCGCGATGGCCGATGCGAGGCAGGGAAGGGCCGGCATCCGAG
>1.2|80539|23|NZ_CP045802|PILER-CR
AATCGGCGATGCAAGGCAAGGAC

CRISPR arrays and Neighbor proteins around NZ_CP045802_1

CRISPR arrays

The CRISPR arrays of NZ_CP045802_1

>merge|NZ_CP045802|1|80411-80585|PILER-CR
GGACGGACATCTGGTGGAGGACGGACGTTAGGGACGGGTCCGCGATGGCCGATGCGAGGCAGGGAAGGGCCGGCATCCGAGGGATGACGGACGTTAGGGACGGACATGTAATCGGCGATGCAAGGCAAGGACGGACGGACATCTGGTGGATGACGGGCGTTAGGGACGGACATGG

>NZ_CP045802|1|1|80411-80585|PILER-CR
GGACGGACATCTGGTGGAGGACGGACGTTAGGGACGGGTCCGC	GATGGCCGATGCGAGGCAGGGAAGGGCCGGCATCCGAGGGAT
GACGGACGTTAGGGACGGACATGTAATCGGCGATGCAAGGCAA	GGACGGACGGACATCTGGTGGAT
GACGGGCGTTAGGGACGGACATGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_153782520.1|63463_67720_-|DUF5057-domain-containing-protein	unknown	unknown	gnl|CDD|374567
NZ_CP045802.1|WP_153782523.1|73991_75485_+|hypothetical-protein	unknown	unknown	gnl|CDD|227306
NZ_CP045802.1|WP_101809382.1|70919_72074_+|type-II-secretion-system-F-family-protein	unknown	unknown	gnl|CDD|224376
NZ_CP045802.1|WP_101808277.1|76436_77255_+|hypothetical-protein	unknown	unknown	gnl|CDD|367091
NZ_CP045802.1|WP_028598290.1|89714_90083_+|GntR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224639
NZ_CP045802.1|WP_028598296.1|96248_96788_+|hypoxanthine-phosphoribosyltransferase	unknown	unknown	gnl|CDD|223707
NZ_CP045802.1|WP_153782522.1|69812_70862_+|PilT/PilU-family-type-4a-pilus-ATPase	unknown	unknown	gnl|CDD|225364
NZ_CP045802.1|WP_153784623.1|90090_91011_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|224054
NZ_CP045802.1|WP_028598288.1|77850_80346_+|stage-II-sporulation-protein-E	unknown	unknown	gnl|CDD|274328
NZ_CP045802.1|WP_127464516.1|88932_89547_-|type-II-toxin-antitoxin-system-PemK/MazF-family-toxin	unknown	unknown	gnl|CDD|367091
NZ_CP045802.1|WP_153782525.1|80695_81520_+|hypothetical-protein	unknown	unknown	gnl|CDD|236545
NZ_CP045802.1|WP_153782527.1|91007_91715_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153782528.1|91836_92871_+|NADPH-dehydrogenase	unknown	unknown	gnl|CDD|239242
NZ_CP045802.1|WP_153782529.1|94667_96194_+|tRNA-lysidine(34)-synthetase-TilS	unknown	unknown	gnl|CDD|238950
NZ_CP045802.1|WP_028598286.1|73216_73975_+|prepilin-peptidase	unknown	unknown	gnl|CDD|377700
NZ_CP045802.1|WP_153782524.1|75474_76236_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153782526.1|82141_88567_+|multifunctional-nuclease/2',3'-cyclic-nucleotide-2'-phosphodiesterase/5'-nucleotidase/3'-nucleotidase	unknown	unknown	gnl|CDD|236505
NZ_CP045802.1|WP_101808275.1|72771_73206_+|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	unknown	unknown	gnl|CDD|225076
NZ_CP045802.1|WP_153782521.1|68029_69694_+|type-II-secretion-system-protein-GspE	unknown	unknown	gnl|CDD|274186
NZ_CP045802.1|WP_028598295.1|93707_94634_+|serine/threonine-protein-kinase	unknown	unknown	gnl|CDD|270916

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_153782520.1|63463_67720_-|DUF5057-domain-containing-protein	gnl|CDD|374567	pfam16480, DUF5057, Domain of unknown function (DUF5057). This family consists of C-terminal of uncharacterized proteins and F5/8 type C domain proteins around 360 residues in length and is mainly found in various Firmicutes species. The function of this family is unknown.	1.15618e-24
NZ_CP045802.1|WP_153782523.1|73991_75485_+|hypothetical-protein	gnl|CDD|227306	COG4972, PilM, Tfp pilus assembly protein, ATPase PilM [Cell motility and secretion / Intracellular trafficking and secretion].	6.90739e-13
NZ_CP045802.1|WP_101809382.1|70919_72074_+|type-II-secretion-system-F-family-protein	gnl|CDD|224376	COG1459, PulF, Type II secretory pathway, component PulF [Cell motility and secretion / Intracellular trafficking and secretion].	2.5628e-116
NZ_CP045802.1|WP_101808277.1|76436_77255_+|hypothetical-protein	gnl|CDD|367091	pfam02452, PemK_toxin, PemK-like, MazF-like toxin of type II toxin-antitoxin system. PemK is a growth inhibitor in E. coli known to bind to the promoter region of the Pem operon, auto-regulating synthesis. This family represents the toxin molecule of a typical bacterial toxin-antitoxin system pairing. The family includes a number of different toxins, such as MazF, Kid, PemK, ChpA, ChpB and ChpAK.	3.85424e-05
NZ_CP045802.1|WP_028598290.1|89714_90083_+|GntR-family-transcriptional-regulator	gnl|CDD|224639	COG1725, COG1725, Predicted transcriptional regulators [Transcription].	2.5079e-26
NZ_CP045802.1|WP_028598296.1|96248_96788_+|hypoxanthine-phosphoribosyltransferase	gnl|CDD|223707	COG0634, Hpt, Hypoxanthine-guanine phosphoribosyltransferase [Nucleotide transport and metabolism].	2.59886e-93
NZ_CP045802.1|WP_153782522.1|69812_70862_+|PilT/PilU-family-type-4a-pilus-ATPase	gnl|CDD|225364	COG2805, PilT, Tfp pilus assembly protein, pilus retraction ATPase PilT [Cell motility and secretion / Intracellular trafficking and secretion].	2.435e-142
NZ_CP045802.1|WP_028598295.1|93707_94634_+|serine/threonine-protein-kinase	gnl|CDD|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	2.10687e-14
NZ_CP045802.1|WP_153782526.1|82141_88567_+|multifunctional-nuclease/2',3'-cyclic-nucleotide-2'-phosphodiesterase/5'-nucleotidase/3'-nucleotidase	gnl|CDD|236505	PRK09419, PRK09419, multifunctional 2',3'-cyclic-nucleotide 2'-phosphodiesterase/3'-nucleotidase/5'-nucleotidase.	2.23418e-122
NZ_CP045802.1|WP_153784623.1|90090_91011_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	8.28173e-55
NZ_CP045802.1|WP_153782521.1|68029_69694_+|type-II-secretion-system-protein-GspE	gnl|CDD|274186	TIGR02538, Type_IV_pilus_assembly_protein_PilF, type IV-A pilus assembly ATPase PilB. This model describes a protein of type IV pilus biogenesis designated PilB in Pseudomonas aeruginosa but PilF in Neisseria gonorrhoeae; the more common usage, reflected here, is PilB. This protein is an ATPase involved in protein export for pilin assembly and is closely related to GspE (TIGR02533) of type II secretion, also called the main terminal branch of the general secretion pathway. Note that type IV pilus systems are often divided into type IV-A and IV-B, with the latter group including bundle-forming pilus, mannose-sensitive hemagglutinin, etc. Members of this family are found in type IV-A systems. [Cell envelope, Surface structures, Protein fate, Protein and peptide secretion and trafficking].	0
NZ_CP045802.1|WP_153782528.1|91836_92871_+|NADPH-dehydrogenase	gnl|CDD|239242	cd02932, OYE_YqiM_FMN, Old yellow enzyme (OYE) YqjM-like FMN binding domain. YqjM is involved in the oxidative stress response of Bacillus subtilis. Like the other OYE members, each monomer of YqjM contains FMN as a non-covalently bound cofactor and uses NADPH as a reducing agent. The YqjM enzyme exists as a homotetramer that is assembled as a dimer of catalytically dependent dimers, while other OYE members exist only as monomers or dimers. Moreover, the protein displays a shared active site architecture where an arginine finger at the COOH terminus of one monomer extends into the active site of the adjacent monomer and is directly involved in substrate recognition. Another remarkable difference in the binding of the ligand in YqjM is represented by the contribution of the NH2-terminal tyrosine instead of a COOH-terminal tyrosine in OYE and its homologs.	1.09371e-169
NZ_CP045802.1|WP_028598286.1|73216_73975_+|prepilin-peptidase	gnl|CDD|377700	pfam06750, DiS_P_DiS, Bacterial Peptidase A24 N-terminal domain. This family is found at the N-terminus of the pre-pilin peptidases (pfam01478). It's function has not been specifically determined; however some of the family have been characterized as bifunctional, and this domain may contain the N-methylation activity (EC:2.1.1.-). It consists of an intracellular region between a pair of transmembrane. This region contains an invariant proline and two almost fully conserved disulphide bridges - hence the name DiS-P-DiS. The cysteines have been shown to be essential to the overall function of the enzyme in, but their role was incorrectly ascribed.	8.3714e-38
NZ_CP045802.1|WP_127464516.1|88932_89547_-|type-II-toxin-antitoxin-system-PemK/MazF-family-toxin	gnl|CDD|367091	pfam02452, PemK_toxin, PemK-like, MazF-like toxin of type II toxin-antitoxin system. PemK is a growth inhibitor in E. coli known to bind to the promoter region of the Pem operon, auto-regulating synthesis. This family represents the toxin molecule of a typical bacterial toxin-antitoxin system pairing. The family includes a number of different toxins, such as MazF, Kid, PemK, ChpA, ChpB and ChpAK.	4.78311e-10
NZ_CP045802.1|WP_028598288.1|77850_80346_+|stage-II-sporulation-protein-E	gnl|CDD|274328	TIGR02865, Stage_II_sporulation_protein_E, stage II sporulation protein E. Stage II sporulation protein E (SpoIIE) is a multiple membrane spanning protein with two separable functions. It plays a role in the switch to polar cell division during sporulation. By means of it protein phosphatase activity, located in the C-terminal region, it activates sigma-F. All proteins that score above the trusted cutoff to this model are found in endospore-forming Gram-positive bacteria. Surprisingly, a sequence from the Cyanobacterium-like (and presumably non-spore-forming) photosynthesizer Heliobacillus mobilis is homologous, and scores between the trusted and noise cutoffs. [Cellular processes, Sporulation and germination].	0
NZ_CP045802.1|WP_101808275.1|72771_73206_+|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	gnl|CDD|225076	COG2165, PulG, Type II secretory pathway, pseudopilin PulG [Cell motility and secretion / Intracellular trafficking and secretion].	2.09641e-09
NZ_CP045802.1|WP_153782525.1|80695_81520_+|hypothetical-protein	gnl|CDD|236545	PRK09510, tolA, cell envelope integrity inner membrane protein TolA; Provisional.	0.00227575
NZ_CP045802.1|WP_153782529.1|94667_96194_+|tRNA-lysidine(34)-synthetase-TilS	gnl|CDD|238950	cd01992, PP-ATPase, N-terminal domain of predicted ATPase of the PP-loop faimly implicated in cell cycle control [Cell division and chromosome partitioning]. This is a subfamily of Adenine nucleotide alpha hydrolases superfamily.Adeninosine nucleotide alpha hydrolases superfamily includes N type ATP PPases and ATP sulphurylases. It forms a apha/beta/apha fold which binds to Adenosine group. This domain has a strongly conserved motif SGGXD at the N terminus.	2.47776e-73

Protein sequences

>NZ_CP045802.1|WP_028598288.1|77850_80346_+|stage-II-sporulation-protein-E
MKEKANVVLFPGQPRTSRAAEALRRGRERAAQWRVFQLIAAKRWTILLAVVGFLLGRAVILENLMPFAPAYFAVIYFLRRDMYKLTAVSLVAGSLLAATPSAIPIAMEIAVLFLLLKGLEVYEKAELSQAPILVFLATLVVKLFGAFVHGTLGWYDLMMVGVESALAFVLTLVFVQAIPVLTMTRKSNSLKNEEIICLMILMASVMTGAVGWSIQGLSLEHILSRYMLLLFAFAGGAPLGASVGVVAGLILSLANLNAVVQMSLLAFSGLLAGLLKEGGRMAVAFGMLLGTSILSLYVGGGMDVMASTWESVVAAALFLLTPKLVVKTISRYVPGTSEHVKSQHEYAKRVREVTAQRVTQFSEVFRQLASSFGQLNTAAPQKPAEEELEHFMNAASSKVCASCHRKDMCWSSKFMDTYKMMTEMMTTIDEGEYTGKKDMPRTWTSHCSKTHPVMNALQQQHERYKHDLHWKRQIFESRQLVADQLAGVSQIMEDLAREIQREGQQLHLQEEQIRDALEALGLSIHGIDIISLEEGNVEIEVYHTFPQGHDEGRKIIAPLLSDILGEHVAVKAEREPLKNGEPRLLRFGSAKEYEVATGIAGAAKGGGLLSGDSFSTVELGNGKFAVAISDGMGNGERARLESSTALSILQQLLQSGMDEQLAIKSVNSVLMLRSPDEMFATVDVALIDLYTAQTTFMKIGSTPSFIKRGSEVIPVAANNLPIGILQDIDVDLIRMQLQPGDTLIMMTDGIYDAPGHAVNKELWMKRIIQEMATDDPQLIADMLLERVVRQYKGEIVDDMTVVVAQVDKHLPEWATFRWPGLSKLERPRTVS
>NZ_CP045802.1|WP_101808277.1|76436_77255_+|hypothetical-protein
MHECLNGHETFGRLDRELQDKLVDQFERLINAEAKVLSQGTDERGKTVYKPSLDRFDIVLVSFIGIGHLMNEPHYAVVWDAPAHSSNLSVFPLSSKVKHPKFAIGPVDTLPAEDTAIMINQLTTVSRRSLIEPVKKRNAAGRLVNVSLTVRQQRQVLALFHETLLKQPTLRSVIEKELGSHIPFGLSDDNRSDLEVPVAYGLHHSLLLYQLPWSKTMKAIPLQAIEMPFGERRRLVRGLLSRDPLQQAEAEAILALKQTGQMAAEAAVGQLS
>NZ_CP045802.1|WP_153782524.1|75474_76236_+|hypothetical-protein
MAARRNSWILLLSAILFLGLLLFFLYGLKPAEEKAASLEAELGTQQKLNDILIAKLQERREEAEIRPVEGVQAELPYWDNTEQLVLDLEQLGAENGVEHVSIAFSGDLAASRPLRSDPSAERSAAPGEGAPAAEGDAAPAVDELGLAAGGSPSSEPQPAGAAAAGPLRLQVSAVVKGTYDAVLKYVQSLHGLTRLTTLESLELSRSSCGCGSEQELTVPLTFAAYFQPTYRDRVETPLLPYAESSVASPPPRS
>NZ_CP045802.1|WP_153782523.1|73991_75485_+|hypothetical-protein
MPALGRKRIGIAIDAAGIRYAPLGKKGLDPEQAGFFPFPPGLIAQDAIVNEESLRLSIREWARERKLQGAVAVLAVPTSQVIVRRMALPAASDRELRQLIHLEVETVMHLPFEHPVYDYVLLEQGGESAQALVYAAPRSWIEPLVAMLREARIRVVGTGIVATALQGAAGFGDEPPCERMHVHLSGAAAEIAMFHEGNPVFVRSIEADGVDQELGGLRIGELTAEITRMLSFYEFGLQEGRSRIRQAVITGAGKQAEALRQSLAAALPEVEFRGAEPGSLAAESLDGRAEPYVVPAGLLVRGSGIRRLNLLPRVDREQRLAPLAAAMLAVAWIACAALLGYSYAGERQAASDAQERLLDASQQQLALQRQLDGLNRQASGAEADPYEQAEQIRAQRRDAAGYVRDLEFYLPTGAELQSIAYSSGGQLSVSVRLGGMKDSSRYLFDIRRIEWLDQATLTSIKQEQTGAENDATPTYAAAYTIVLKPTEPTKEGTADGS
>NZ_CP045802.1|WP_028598286.1|73216_73975_+|prepilin-peptidase
MTLLISLYLFALGLACGSFFNVVALRVPLGQSVVRPPSACPHCGHRLAARELVPVLSYALSRGRCRSCAAPVSPLYPAGELAAALLFVWAYLRFGLTAQGLIGLLLASLAVIVTVSDIRYMRIPNAVLLAFLPPLLLLRLLEPDGRSYAEYALGAIAGGGVLLLVALLSRGGMGMGDVKLLALIGLALGWKGALLTLLLGSFAGTAAGLVLLLRRRSKLRQPMPFGPFLMLGALIAYGYGDALIGSYLQLFK
>NZ_CP045802.1|WP_101808275.1|72771_73206_+|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein
MTAILKKLKKDEKGFTLIELLAVIVILGIIAAIAIPVISNIMNKSRDKSDIATAQQIYDAARMYVSTELNGDFKGKDIKIVGGTGDTLVSKNYLDAGLRLPSTKAVITGGEVKFKADGTLDSVTISTDEAATTEDKVYQAADLK
>NZ_CP045802.1|WP_101809382.1|70919_72074_+|type-II-secretion-system-F-family-protein
MLTAMDKSSAVEELRRRGLVVLALEEHRSSLLQMDIYIGNPVKPAHFIVYCRQFATLVRAGVPIVQATDILSQQTESKPLRKALRDVHASLLRGSSFSQAAMEHRRIFPVMFTSMIRAGEESGDLEGTLERLATFFEKGHVTREKIKSALTYPVIVGLLAVAAVIYLLKAIVPQFVSMFESMNAELPAITKVVMALSASIENEWYLWLGAAVLLLALLLGFKRTQRGAYALDYVKLKLPVFGKLQQKGAIAQVSRTLSSLYASAVPMLQSLQIVEEAVGNRVIARYLRLSADSLRRGNPLSEPLKQSWVFPPLVTQMIAVGEETGALDEMLAKVADFYEMDVDNTVDRLKSLIEPLLIVFLAGVVGLIVAAIMLPMFSLYGQMG
>NZ_CP045802.1|WP_153782522.1|69812_70862_+|PilT/PilU-family-type-4a-pilus-ATPase
MNEPQGLLRELLREARERGASDLHLAAGAPPLLRIDGALAPAVSLAAPLGREQAEALLLPLLGSRRERFDAEGEADLACEADGSRYRLNVFRRLGGLGLAARVLPDGTPTLEELGLSRMLTDWAQRRQGLLLVTGPTGSGKSSTLAALVGHLSRTRSLHIVTLEDPIEHVYPQERSLIDQREIGRDTASFASGLRAALRQAPDVILVGEMRDAETMAAALTAAETGHLVLSTLHTADAPQAVDRIVDAFGADRQGQIRAQLASLLIGVHAQRLLRRAGGRGRVCAAEILVNTPAVANLIRTEKVHQLRGVMQTGRQQGMATLESSVQELLRQGAADPADARAYLQERGE
>NZ_CP045802.1|WP_153782521.1|68029_69694_+|type-II-secretion-system-protein-GspE
MNRVRKRLGDLLVESGVITETELQEALREQGRTKQKLGDLLIAQGYMTEQQLIEVLEFQLGIPHVSLFKYQIDPSIAQIIPESLARRYQVIPLHKEGGKLMVAMADPLDYFAIEELRMSTGFRIEPAISTKEELQRAIARFYGLQDSMSQILGELPTQDEIGEMEITDEDSPVVRLVNGMIQQAVQLQVSDIHVDPGETQVLIRYRIDGELRTERVIPKAMQGYITARLKIMAKLNIAERRLPQDGRIKMQVDFRTVDIRISSLPTIHGEKLVLRILDLSVGVKGIEQLGFSPDNYRLFKGMVESPYGIVLLTGPTGSGKTTTLYSALQHLNRDSENIITVEDPVEYQLEGINQVHVNPAIGLTFAAGLRSILRQDPNIVMVGEIRDSETAEIAIRASLTGHLVLSTLHTNDAVSTVTRFRDMGIASYLIASSLVGVVAQRLVRRICPDCRQAHEPTEQERILLRSYGIETDRLYRGAGCGSCSKTGYRGRIAIHEVLAVTDELRRMIGDDASVLELREAAERAGLAGLLQDGMDKVLQGQTTVQEVMREAALR
>NZ_CP045802.1|WP_153782520.1|63463_67720_-|DUF5057-domain-containing-protein
MLPMAARLRSALCAPLAILLLLASLLSLWPPSVPSASAASAAKIRLLELTDAGTSDLKPLLGSADYEITTMKMKTFVASRVDIDGLYDAVYIGKGKYNPESMSYLSTSDARNAAHDTSKKLNDITNLKAQELIDGYVNRGLLVLLYSDKATSDGLLYQPALPNGESGVLKKRFSIYQESGKQRENVLFLDKQGLSAIASTLKQNKYARLLSLRPELNVTEAPTDYVTNPSHFYRAGDTLVFRYEQPAESRLRANLYLNLDASLRFQAEQVVATSDASGPSGELRYRMPRGYSGLYYWKLELVELETGLKSYASGAVRFRDRQTEISVLQVLPGNANSDLTKDTVLKQSYLSTEDYRIALKTATIQAFNTKGGPYGYDSIGGKYDMLIFGFKDSYNGSAPISETAAKAVKDFIETGQSVLFTHDTVFISDGTTDNVWTRNFKPVTGQTGLHTNIGLGAPKTSSTVAKVNDGLLTKFPFNLDAGTPSVATTHDQYFMLDLEDPTLVPWYNITGGTRDNSDSWNHYYTYSKGNVTYSGTGHQGDSGTFPDWEQRLFVNTMYRAFMGSNHKPELAVHAPAAYSAQAGNYIPHYQQIPVSFTAEDPDYKDRRISAKVEFLYTGTDGKPVVRTMSENASLLSGTLVSESYPNPLPQGGELTVRITATDRQGAFSTESVRVVVRPVTAGLQVDRSVTGTFKEAYVEKGKDFTLSYVVRPQPVTAAKGQSDLVIAAPAFQEKLPPNLEPVSLPPGFQKSGTLASGYTVTGTLPDIRYAADPSGDGTRYVADQVPFSITAKAAAIGRLPLDQATLTYRNLGQIAGTSLRFNALTLEAIVKPTALSLPAEVDIAFGQSFKLLLTMDPAEASVIGLKWTTSQPAHVSIEESVIGGIMVKGLKIGQSSVVQVTDELTGLSASTKVNVIQPGLSLSTADGASVYTLGSRIGLKSVLTKVTSDVVPSGAQVEWSVSPQQAGAESIRERQRTPGVWEWTSGFYPSSPGTYTLRARLTVQGLNDKGELVSRTYESPEPELKLDIVAPDLQVSGPAVIVAGDSAASWTRNWGDRRPVGTDVPGRALTYAWSWEPSAGPSKSLPADSGYQSVRMDPSLTGSGHVALKVTQPLQAGQTPIELAKAAQPVRIIAKPALAAGKSELLPGEQTQLSLRWDGVAAADIPEHTVSWTVSGSGTLQGDAANSRTLTASKPAGSSGKAKAAAIVTMATGYSFTVERELGVFAPELALSALPERLAAGQQLTVSASWSPAYSGSLSALIWSLGGAPADRATLAPIAGNPAKALLSAVSPGSATVTGSIELGSGYRSSVSKSVLIGDFSLPAALTLEQGAQLPLRTSGLQAQPSSLASEILGALRWGSSSPAVVSVDASGRLTAKKPGSAVISAVWRANGLPGGSLQRTIAVTVKAPSGERLGDRY
>NZ_CP045802.1|WP_153782525.1|80695_81520_+|hypothetical-protein
MTTLIRRNPGSARSRKKRESLQQKQQQRLEEQLRLQEQQQLEAARRRREQEREKRREAEARLEELRLEELLMREMERMRLAADKKRGKRLWTAEERMAQRAFAAALMETAAAAQAEREAERSGYAEGWMPAAAAAGGRRPGGAGGARTAAAERTSSRAQLELVAKPPAQPHGGGRGRAAGGMAPPGTGGAAEARQGDAAPGALPLGRASAGQLERLAADVLAAAGSGRRRSRAAQALRRRRGPVRSPCGGEEGRLRLVRPGRPPGKEARGGKPR
>NZ_CP045802.1|WP_153782526.1|82141_88567_+|multifunctional-nuclease/2',3'-cyclic-nucleotide-2'-phosphodiesterase/5'-nucleotidase/3'-nucleotidase
MNIHLCKLKFSAIINAISSIILKELTTLPSHPVSFLIRSKRNISLFTVLALLATLLLPAGMATTVRAAAAGHVVISQIFGAGGNGGALYNADFIELYNPTSETVSLADWKLDYASSAGSYPASAPNSNILMLSGSIAPGGYFLTKQSGGANGAALPAPDATGTLALAAASGKVRLSDASGNIVDMVGYGTAATPFEGSGPTGNLSATTAAIRKASVTGGNDRGQDTDNNVADFDIAAPAPRNSASPSDVPSVVTVQPVTGSPAPNAWPAGTAVTLSTATAGASVYYSTSADSTYRAFTSPIVLTESVTFHTYAAKEGAEGSISRDLAYDVLAKQSVADARLAPVGRNVWTEGVVTAVNGREVYLQDNTAAIVLYDYPDQLRAGDRVSVQGEMVHYNNLQELKPAAGLSLEILERDQPVPAIRAVTPEQLAAPAGEALEAQFISIDNVTIGAKSGSTWSAKQAGSDTSFAIFSSSAKVKENAAFDRVIGVVKQYQGIYQLVPLHDGMLVDQLFTVLASPAGGIVAPGTRVALSVPAGDLPIRYTTDGSEPTASSPLYEESILVDRAMTIRAFATDGEQRTETLSFSYQLAGEVGIRDIQGKGHASPFVGQTIQGVKGVVTQLGYNLASATPSYKGFYIQTLEPDNDPATSEGLFVYSTDASKKPAVGDVVEVSGKIDEYNEGLATNLTTTQLALASISVLESGHELPAPVVLGAGGRVIPTPTIDDDSMTVFDPENDAIDFFESLEGMRVQAPAPVITSPYWITSGLYTIATRIDNGGADLVTPAGGLALGAYKDYNPQRVLILSSNPGFEVGTGDRFAGDVVGALGYHAGNFKLIPAPGSLPAIETSSFAQETTTLQPEGDKLLVASYNIENFYPGVKAEKIEKLGDSIAHNLKAPDIITVIEMQDRNGETDNGIVEADATALIQSIAAKGGPTYTYVDIAPVNKEDGGAPGGNIRVGFLYNAERVQLADSVQGRKGGSTEATAYDAASDSLTLNPGRVDPTNAAFASSRKPLAAQFVFQGRKVIVVANHFNSKTGDQGPFGAAQPPFLSSETTRWEIATLVNGFVKTIVQANPEANVIVTGDLNDFQFTPTAEKLKGGELANLIDTLPAGEQYTYTYDGNSQVLDHILVSRNLLVGSKVDVVHLNADFPESRGRVSDHDPVLAQIDLTPAPKPDFRMTLLHTNDTHANLDTTSAPSSVARRVTAVKEQRASAVNPLLVDAGDVFSGTLYFNKYEGMADLAFMNLMKYDAMTFGNHEFDKNADVLARFVQGAAFPFVSSNVDFSGEAALQALVRPAAGAGQAVAGKIYPTMIKEIGGEQIGLIGLTTPDTANIASPGAVTFADPAVSAAAAVKQLQEQGIDKIIALSHLGYEEDIELAQAVAGIDVIVGGHSHTKLEQAVVDRTFEAPTLIVQTGEKGQFLGRLDVAFDKEGVISEYADKLISIEEKNGSADVLANDPEAEALLKNDYKPGVDALGREEVAKSTVVLNGVRDDVRTKETNLGRLIADGMLSAARKAGANATLALQNGGGIRASIEAGTITLGQVLTVLPFNNDLVTVKLTGKEIREALENGVSKLPASDGRFPHVAGMRFYYDSLKPAGSRVVKIETLQPDGSYVAMKEDATYELATNAFTARGGDFYDSLAKAYNEGRVVPLYLPDYEVMEAYLKEKKTIDESTAPAGRIIDLKGSPLPVDPTPTPTSTTTPTPTPTSTTTPTPTPTSTTTPTPAPTSTATPTGTATPQPTASTTPAPTAKPGAITAPLQLSEQAGLTVGTATVGAEQALAALQAAADGKLTIAASAAGSFDRTEVTLASGTVAALLGAPSFREAAVSSPQGSYVLTRALLESLAKGAANAALTVKIGSAQAGLDLAKAAGLPAIGAAEYELALTVDGKTSEPNRFGSYVPRSLRLADTAAVTAIVRLSSDASGQLAYVPVPFIVQDGQIVFFSRGNSSYVALGGAAAAFADMHGHWAAAAVQELAGKRIVAGKTASAFAPGDAVTRAEFAVLLARTLGLTAGSAASFTDIAAGAWYADGIAAAAEAGLIGGYEDGSFRPQQRITRQEMAVMTLRAVQLAGRQASAPQAEAVAFADSGRIASWAQAAAAELSRYGLIQGDDQGRFQPLAGATRAESAALLQRLLAQASFE
>NZ_CP045802.1|WP_127464516.1|88932_89547_-|type-II-toxin-antitoxin-system-PemK/MazF-family-toxin
MTILKEDAHWHSILKERIADLERTIENMGLKRGKIFLEWMETQNKYLKWETGFEPSKLRKYNRGEIIFVNFGFNPGSEIGGLHYAVVVDENEKSNPVVNVVPLGSLENSQPRSILHKHEIYIGVLEDLNGKEAFAIPNQLQPISKLRIYKPRRAADKVFKLPAPFLDLIDNKILELFTPRYSSAIKLMEQATNTAAASRENDSQ
>NZ_CP045802.1|WP_028598290.1|89714_90083_+|GntR-family-transcriptional-regulator
MSFLKDDGRPIFQQIAEKIEDDIVDGSLPEEGQAPSTTHFAQFYGINPATAAKGVNLLVDQGILYKKRGIGMFVAEGARERLMERRREQFYEQYVVPLLREAEKLGIDSGRLAAIIQEKGRG
>NZ_CP045802.1|WP_153784623.1|90090_91011_+|ATP-binding-cassette-domain-containing-protein
MTVKDRTQAAYALEADRLTKSYGAQKALDGVSLKLEAGLIHGLLGRNGAGKTTLMSIATAQLFATSGEVRIFGQQPYENREALSKICFIKESQRYPDMFHVEDVLATARALYPNWDEALAGELVESFRLPRRKKIKGFSRGMLSSVGIVVGLSSRAELTLFDEPYLGLDAVARSLFYDRLIEDYAEHPRTVVLSTHLIDEVSRLLEAIHVIDGGRLLLSEDAESLRSRAYRVSGSAAKVDAVTAGRRVLRRETIGGSAVASVLAGEPGENGIALALEAGLEAEPLPLQQLIVDLTAHAARGKEESA
>NZ_CP045802.1|WP_153782527.1|91007_91715_+|hypothetical-protein
MNRGLKSILTMYRRDKFNWLLLPWLILLSSFTVNLVVAFSMNRGGGEESFTTGGLLSIIIYMFIVGMISVYWTFNFALSLCISRRDYFTGSGIAFLAMSAFHGALLTVATSIEQAIGGWFGMHFFVIPYTTDGPFWQTFAVYFTVLLFAGYGGFVSGSLSRRYGKRGNFLLYGGTFILGGAFTTIASLRGWWVPIFDWISGLQISLQGVCLLLLALAVLFATLSWLMLRRSSARA
>NZ_CP045802.1|WP_153782528.1|91836_92871_+|NADPH-dehydrogenase
MAKLSEPFRLKGLELKNRIVMAPMCQYSVEEQDGTPNDWHFVHYVSRAVGGTGLIIMEMTNVEPDGRITSRCLGLWDDAQIPAYARIVRECQRYGARVGVQIAHAGRKATDAEQPVSSSPIPVEPTGWKTPRELTTAEVRGQVGLFREAARRAVEAGFDTIELHGAHGYLIHQFHSPSLNRRTDEYGQDKLRFGCEVIAAVREVMPADMPLILRFSATEYIEGGYELDYGLEIARRYKEAGVDILHVSSGGEAPPNGKRQPGNYPGYQVPMARAVREAAGIPVIAVGMLDEPELAQSVVQSGDADLAGIGRALLRNPYWAVDALLKTEGLRTEQPAYKRGYPLK
>NZ_CP045802.1|WP_028598295.1|93707_94634_+|serine/threonine-protein-kinase
MATSAKLDLDRGMVITGKWRRRRYRVERMLGEGANGKVYLVQQEGRLLALKVGMDTADLQSEINVLKALEKQQPRGGGASPYLLDVDDLKLVSGKEYPFYVMRYVRGAKLPAFLAASGDEWFPLAGYNLLLRLAELHASGWAFGDLKIDNVLAAEYGRVELIDYGGVTAFGKGIRQFTEIYDRGYWNAGTRASDAGYDLFSFAVLCVQLFAEKELHRAASGTLPQNRSAGDVLKLAQDAPQLRPFSGWLARALAGGFADAAEASHAWKAVMHRVSRPAKPVPWWTKALFLAAAAGLAASAFWLGGGLG
>NZ_CP045802.1|WP_153782529.1|94667_96194_+|tRNA-lysidine(34)-synthetase-TilS
MASTDSGQPDRTRPEPLRPPASAGDPDRVRRELLRMGADERLWEPGDTVLVAVSGGPDSMALLHALHAAAPQLGVSVAAAHADHGFRPQASAREAETVRGFCARLGVPCDTAELDVPAHLAEHGGNKQAEARRLRYRFLLEAAERAGAPRIALAHHADDQAETVLMRLLRGSSSAGLSGIPLRRQEGKAELIRPLLRIHKPDLLAYCERHGVPYEEDASNRSADYTRNAIRLEAMPYLETFNGRLAESLCRTAESASAESDYLDARTKEVFASSVVSERGGLTMSGAAFAALHVALQRRLIKLILDYLALEMAPSSFDEVERIRVGALSGTPASWRVDLSRGLRFRREYGRLAWTRRADEKPLPYAVEIPEPDGVWTIAEAGLEIRFSAHRHTRDGTARFAASDADARTAFFDWDKLELPLLLRPRRSGDRMRPLGLNGTKKVQDMFVDGKLPPSRRPFLPLLCDGGGRILWIPGLRRSSHALADEGTRLLLRAEVRPAGGSSEPAGE
>NZ_CP045802.1|WP_028598296.1|96248_96788_+|hypoxanthine-phosphoribosyltransferase
MHNDIQEILHSEEEIRDKVKELGEILTRDFEGRNPLVICVLKGAFIFMADLVKEIRVPLEMDFMAVSSYGASTKSSGVVKIIKDLDVSVEGRDVLIVEDIIDSGLTLSYLIDVLERRNAKSVTVVTLFDKPSGRSVDLNADYTGFTLPHAFVVGYGLDYAEYYRNLPYIGILKPEVYRK

Crispr_ID: NZ_CP045802_2

• CRISPR_ID: NZ_CP045802_2
• CRISPR_location: 416954-417300
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 6 spacers

Consensus repeat of NZ_CP045802_2

Consensus_repeat	Method
AAAGGCGACAANGGCGACACCGG	CRT

spacers of NZ_CP045802_2

>2.1|416977|22|NZ_CP045802|CRT
AGACAAAGGGGACAAAGGGGAC
>2.2|417022|49|NZ_CP045802|CRT
CTCGCCCGGCCCTGCAGGAGCGCCTGGCGCGACCGGCGCTCAAGGCGAC
>2.3|417094|40|NZ_CP045802|CRT
CGCGCAAGGTCCGGCGGGTCCGAAAGGCGACAAAGGGGAC
>2.4|417157|22|NZ_CP045802|CRT
TCCGGCGGGTCCGCAGGGCGAA
>2.5|417202|31|NZ_CP045802|CRT
AGCGCAAGGCCCGGCGGGTCCGGCAGGAGCT
>2.6|417256|22|NZ_CP045802|CRT
CGCAACGGGTCCGGCGGGCCCG

CRISPR arrays and Neighbor proteins around NZ_CP045802_2

CRISPR arrays

The CRISPR arrays of NZ_CP045802_2

>merge|NZ_CP045802|2|416954-417300|CRT
AAAGGGGACAAGGGCGACAAGGGAGACAAAGGGGACAAAGGGGACAAGGGCGATAAAGGCGACACCGGCTCGCCCGGCCCTGCAGGAGCGCCTGGCGCGACCGGCGCTCAAGGCGACAAAGGTGAAAAAGGCGACGCCGGCGCGCAAGGTCCGGCGGGTCCGAAAGGCGACAAAGGGGACAAAGGCGACAAAGGCGACACCGGTCCGGCGGGTCCGCAGGGCGAAAAAGGCGACAAGGGCGACACCGGAGCGCAAGGCCCGGCGGGTCCGGCAGGAGCTAAAGGCGACAAGGGCGACACGGGCGCAACGGGTCCGGCGGGCCCGAAAGGCGACAAGGGCGACACCGG

>NZ_CP045802|2|1|416954-417300|CRT
AAAGGGGACAAGGGCGACAAGGG	AGACAAAGGGGACAAAGGGGAC
AAGGGCGATAAAGGCGACACCGG	CTCGCCCGGCCCTGCAGGAGCGCCTGGCGCGACCGGCGCTCAAGGCGAC
AAAGGTGAAAAAGGCGACGCCGG	CGCGCAAGGTCCGGCGGGTCCGAAAGGCGACAAAGGGGAC
AAAGGCGACAAAGGCGACACCGG	TCCGGCGGGTCCGCAGGGCGAA
AAAGGCGACAAGGGCGACACCGG	AGCGCAAGGCCCGGCGGGTCCGGCAGGAGCT
AAAGGCGACAAGGGCGACACGGG	CGCAACGGGTCCGGCGGGCCCG
AAAGGCGACAAGGGCGACACCGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_153782626.1|407893_408298_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153782627.1|409072_409726_+|transcriptional-regulator	unknown	unknown	gnl|CDD|377981
NZ_CP045802.1|WP_153782644.1|428880_429057_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153782633.1|415180_415381_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_052333351.1|429569_430778_+|peptidase-S8	unknown	unknown	gnl|CDD|173810
NZ_CP045802.1|WP_153782639.1|422343_422616_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153782628.1|409709_410852_+|amino-acid-aldolase	unknown	unknown	gnl|CDD|143494
NZ_CP045802.1|WP_028599369.1|419754_420441_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_CP045802.1|WP_153782630.1|410868_412500_+|amidohydrolase-family-protein	unknown	unknown	gnl|CDD|226179
NZ_CP045802.1|WP_146000487.1|429031_429220_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153782632.1|413845_414592_+|glucose-1-dehydrogenase	unknown	unknown	gnl|CDD|187600
NZ_CP045802.1|WP_153782634.1|415519_416182_-|TetR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP045802.1|WP_028599365.1|412629_413094_+|RidA-family-protein	unknown	unknown	gnl|CDD|100006
NZ_CP045802.1|WP_153782631.1|413394_413637_-|DUF3977-family-protein	unknown	unknown	gnl|CDD|289867
NZ_CP045802.1|WP_153782642.1|423350_425063_+|PH-domain-containing-protein	unknown	unknown	gnl|CDD|225962
NZ_CP045802.1|WP_153782638.1|420437_422123_+|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|274368
NZ_CP045802.1|WP_028599361.1|408294_408762_-|VOC-family-protein	unknown	unknown	gnl|CDD|319898
NZ_CP045802.1|WP_153782640.1|422569_423361_+|PH-domain-containing-protein	unknown	unknown	gnl|CDD|225937
NZ_CP045802.1|WP_153782637.1|418136_419534_+|hypothetical-protein	unknown	unknown	gnl|CDD|375999
NZ_CP045802.1|WP_153782643.1|426915_428754_-|SgrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|173872

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_153782627.1|409072_409726_+|transcriptional-regulator	gnl|CDD|377981	pfam08348, PAS_6, YheO-like PAS domain. This family contains various hypothetical bacterial proteins that are similar to the E. coli protein YheO. Their function is unknown, but are likely to be involved in signalling based on the presence of this PAS domain.	3.46505e-51
NZ_CP045802.1|WP_052333351.1|429569_430778_+|peptidase-S8	gnl|CDD|173810	cd07484, Peptidases_S8_Thermitase_like, Peptidase S8 family domain in Thermitase-like proteins. Thermitase is a non-specific, trypsin-related serine protease with a very high specific activity. It contains a subtilisin like domain. The tertiary structure of thermitase is similar to that of subtilisin BPN'. It contains a Asp/His/Ser catalytic triad. Members of the peptidases S8 (subtilisin and kexin) and S53 (sedolisin) clan include endopeptidases and exopeptidases. The S8 family has an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure and are not homologous to trypsin. Serine acts as a nucleophile, aspartate as an electrophile, and histidine as a base. The S53 family contains a catalytic triad Glu/Asp/Ser with an additional acidic residue Asp in the oxyanion hole, similar to that of subtilisin. The serine residue here is the nucleophilic equivalent of the serine residue in the S8 family, while glutamic acid has the same role here as the histidine base. However, the aspartic acid residue that acts as an electrophile is quite different. In S53 the it follows glutamic acid, while in S8 it precedes histidine. The stability of these enzymes may be enhanced by calcium, some members have been shown to bind up to 4 ions via binding sites with different affinity. There is a great diversity in the characteristics of their members: some contain disulfide bonds, some are intracellular while others are extracellular, some function at extreme temperatures, and others at high or low pH values.	1.41275e-111
NZ_CP045802.1|WP_153782628.1|409709_410852_+|amino-acid-aldolase	gnl|CDD|143494	cd06820, PLPDE_III_LS_D-TA_like, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzymes, Low Specificity D-Threonine Aldolase-like. This subfamily is composed of uncharacterized bacterial proteins with similarity to low specificity D-threonine aldolase (D-TA), which is a fold type III PLP-dependent enzyme that catalyzes the interconversion between D-threonine/D-allo-threonine and glycine plus acetaldehyde. Both PLP and divalent cations (eg. Mn2+) are required for catalytic activity. Low specificity D-TAs show similarity to bacterial alanine racemase (AR), which contains an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain. AR exists as homodimers with active sites that lie at the interface between the TIM barrel domain of one subunit and the beta-sandwich domain of the other subunit. Based on its similarity to AR, it is possible that low specificity D-TAs also form dimers in solution. Experimental data show that the monomeric form of low specificity D-TAs exhibit full catalytic activity.	1.80149e-124
NZ_CP045802.1|WP_028599369.1|419754_420441_+|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].	6.54039e-75
NZ_CP045802.1|WP_153782630.1|410868_412500_+|amidohydrolase-family-protein	gnl|CDD|226179	COG3653, COG3653, N-acyl-D-aspartate/D-glutamate deacylase [Secondary metabolites biosynthesis, transport, and catabolism].	1.76723e-119
NZ_CP045802.1|WP_153782638.1|420437_422123_+|HAMP-domain-containing-protein	gnl|CDD|274368	TIGR02966, Phosphate_regulon_sensor_protein_PhoR, phosphate regulon sensor kinase PhoR. Members of this protein family are the regulatory histidine kinase PhoR associated with the phosphate ABC transporter in most Proteobacteria. Related proteins from Gram-positive organisms are not included in this model. The phoR gene usually is adjacent to the response regulator phoB gene (TIGR02154). [Signal transduction, Two-component systems].	5.83486e-42
NZ_CP045802.1|WP_153782634.1|415519_416182_-|TetR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.94909e-09
NZ_CP045802.1|WP_028599365.1|412629_413094_+|RidA-family-protein	gnl|CDD|100006	cd02199, YjgF_YER057c_UK114_like_1, This group of proteins belong to a large family of YjgF/YER057c/UK114-like proteins present in bacteria, archaea, and eukaryotes with no definitive function. The conserved domain is similar in structure to chorismate mutase but there is no sequence similarity and no functional connection. Members of this family have been implicated in isoleucine (Yeo7, Ibm1, aldR) and purine (YjgF) biosynthesis, as well as threonine anaerobic degradation (tdcF) and mitochondrial DNA maintenance (Ibm1). This domain homotrimerizes forming a distinct intersubunit cavity that may serve as a small molecule binding site.	1.82665e-77
NZ_CP045802.1|WP_153782631.1|413394_413637_-|DUF3977-family-protein	gnl|CDD|289867	pfam13122, DUF3977, Protein of unknown function (DUF3977). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are approximately 80 amino acids in length.	2.76928e-21
NZ_CP045802.1|WP_153782642.1|423350_425063_+|PH-domain-containing-protein	gnl|CDD|225962	COG3428, COG3428, Predicted membrane protein [Function unknown].	1.64428e-56
NZ_CP045802.1|WP_028599361.1|408294_408762_-|VOC-family-protein	gnl|CDD|319898	cd06587, VOC, vicinal oxygen chelate (VOC) family. 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 is found in a variety of structurally related metalloproteins, including the type I extradiol dioxygenases, glyoxalase I and a group of antibiotic resistance proteins. 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). Type I extradiol dioxygenases catalyze the incorporation of both atoms of molecular oxygen into aromatic substrates, which results in the cleavage of aromatic rings. They are key enzymes in the degradation of aromatic compounds. Type I extradiol dioxygenases include class I and class II enzymes. Class I and II enzymes show sequence similarity; the two-domain class II enzymes evolved from a class I enzyme through gene duplication. Glyoxylase I catalyzes the glutathione-dependent inactivation of toxic methylglyoxal, requiring zinc or nickel ions for activity. The antibiotic resistance proteins in this family use a variety of mechanisms to block the function of antibiotics. Bleomycin resistance protein (BLMA) sequesters bleomycin's activity by directly binding to it. Whereas, three types of fosfomycin resistance proteins employ different mechanisms to render fosfomycin inactive by modifying the fosfomycin molecule. Although the proteins in this superfamily are functionally distinct, their structures are similar. The difference among the three dimensional structures of the three types of proteins in this superfamily is interesting from an evolutionary perspective. Both glyoxalase I and BLMA show domain swapping between subunits. However, there is no domain swapping for type 1 extradiol dioxygenases.	3.78374e-10
NZ_CP045802.1|WP_153782632.1|413845_414592_+|glucose-1-dehydrogenase	gnl|CDD|187600	cd05341, 3beta-17beta-HSD_like_SDR_c, 3beta17beta hydroxysteroid dehydrogenase-like, classical (c) SDRs. This subgroup includes members identified as 3beta17beta hydroxysteroid dehydrogenase, 20beta hydroxysteroid dehydrogenase, and R-alcohol dehydrogenase. These proteins exhibit the canonical active site tetrad and glycine rich NAD(P)-binding motif of the classical SDRs. 17beta-dehydrogenases are a group of isozymes that catalyze activation and inactivation of estrogen and androgens, and include members of the SDR family. 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 have a 3-glycine N-terminal NAD(P)(H)-binding pattern (typically, TGxxxGxG in classical SDRs and TGxxGxxG in extended SDRs), while substrate binding is in the C-terminal region. A critical catalytic Tyr residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering), is often found in a conserved YXXXK pattern. 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) or additional Ser, contributing to the active site. Substrates for these enzymes include sugars, steroids, alcohols, and aromatic compounds. The standard reaction mechanism is a proton relay involving the conserved Tyr and Lys, as well as Asn (or Ser). Some SDR family members, including 17 beta-hydroxysteroid dehydrogenase contain an additional helix-turn-helix motif that is not generally found among SDRs.	1.80479e-95
NZ_CP045802.1|WP_153782640.1|422569_423361_+|PH-domain-containing-protein	gnl|CDD|225937	COG3402, COG3402, Uncharacterized conserved protein [Function unknown].	2.23349e-33
NZ_CP045802.1|WP_153782637.1|418136_419534_+|hypothetical-protein	gnl|CDD|375999	pfam18573, BclA_C, BclA C-terminal domain. This is the C-terminal domain of BclA (Bacillus collagen-like protein of anthracis) which is expressed on spores of Bacillus species. Trimers of the C-terminal domain (CTD) form the tips of the spore's hair-like nap and are the immunodominant target of vertebrate antibodies and drive trimerization. Structure analysis indicate the C-terminal region of the peptide folding into an all-beta structure with a jelly-fold topology, similar to the first human complement C1q, a member of the tumor necrosis factor (TNF)-like family. The C-terminal globular domain has been shown to be located on the exterior of the exosporium, and therefore is critical in determining the immunogenicity of the spore in a mammalian host.	7.88477e-17
NZ_CP045802.1|WP_153782643.1|426915_428754_-|SgrR-family-transcriptional-regulator	gnl|CDD|173872	cd08507, PBP2_SgrR_like, The C-terminal solute-binding domain of DNA-binding transcriptional regulator SgrR is related to the ABC-type oligopeptide-binding proteins and contains the type 2 periplasmic-binding fold. A novel family of SgrR transcriptional regulator contains a two-domain structure with an N terminal DNA-binding domain of the winged helix family and a C-terminal solute-binding domain. The C-terminal domain shows strong homology with the ABC-type oligopeptide-binding protein family, a member of the type 2 periplasmic-binding fold protein (PBP2) superfamily that also includes the C-terminal substrate-binding domain of LysR-type transcriptional regulators. SgrR (SugaR transport-related Regulator) is negatively autoregulated and activates transcription of divergent operon SgrS, which encodes a small RNA required for recovery from glucose-phosphate stress. Hence, the small RNA SgrS and SgrR, the transcription factor that controls sgrS expression, are both required for recovery from glucose-phosphate stress. Most of periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.31687e-108

Protein sequences

>NZ_CP045802.1|WP_153782634.1|415519_416182_-|TetR-family-transcriptional-regulator
MDSEEEAETMKPAKVDPRVQRTRRLLREALVQLTEERGLDGFSVQELADRATVKRATFYLHYEDKQALLADYIAELLEELRVAVFDPGGQPPDYDYASGEPHPSFVRLFRHLAERYDVYHALLVRRRVPELAAGMLEVVRQFVAEGLAFAQPDDRLLTARRDVTLKYTEAAYVEVIIWWIEQQMPYAEKEIAAQLMDLSIFGPYRELPAWAGSGREKTSG
>NZ_CP045802.1|WP_153782633.1|415180_415381_-|hypothetical-protein
MLQRREELQAILDRAADQARTEAKRAGASIYYIREKKRIRESADGKKFEIMIDESGNRVERVLHEP
>NZ_CP045802.1|WP_153782632.1|413845_414592_+|glucose-1-dehydrogenase
MGRLTGKTAIITGAATGMGAEEARLFAREGAQVVLTDVNLDAMNQVAEEIKAAGGEALALRHNVASEEEWTKVVEETVARFGKVDILVNNAGISARTTIGNLDLAEWQRVLDINLTGCVVGMKAVIPEMQKAGAGSIINISSIGGIVGMAGSSAYTAAKGGLRTLTKAAAVEYAKQSIRVNSVHPGIIVTPMTEPSMKDAMPYYQTFTQLPYFGKPEDVAYGVLFLASDESRFMTGSELVIDGGWTAL
>NZ_CP045802.1|WP_153782631.1|413394_413637_-|DUF3977-family-protein
MKYIEAGIGNRWWLRTEIEHADGTEEERRGAVGPIRIRSLYVRLWIGRRVYILDTRDGWKSGRKRQKRFKLVLGLCGFME
>NZ_CP045802.1|WP_028599365.1|412629_413094_+|RidA-family-protein
MSIIEKRLAELGITLPELPAPKFSYIPVNRTGNLIYTSGFDCRIDGVLLYEGKVGSDLTIEQGQEAARQVVVNLLAAMKAYLGDLDRVVKIVKLLGFVNSAPGFGDQPYVMNAASDLLIEVFGENGRHARSAIGTSDLPFHTPVEIELIAEIRD
>NZ_CP045802.1|WP_153782630.1|410868_412500_+|amidohydrolase-family-protein
MLDLVLKNGRIVDGSGNPWYRGDVGVKDGRIAAVGRIDEEAAATVDVRGQVIAPGFIDGHCHSDLMILDHPLSEIKLSQGVTAEVVGNCGLAPAPVFPDREELLRSYISPVIGSTKQDWQWNTVGEYMDYVGRSAPAEHMATYVAHGALRIAVMGFDNRPATPAELQRMKELLEEGLRAGAIGLSIGLLYSPGSYTSKEELAELCSVLPRYDGLLSTHIRGEGNNLLPSVREVIWIAEQAGIPLHVSHLKAAGKANWGKALEAMELVEDARARGMDVTVDVYPYNAGSTSLTTILPPWVLEGGIPGALEAFRDPALRRRIREELGREQDDWDNLVCSTGWQSVFVASASGANAGLEGKHIAEIAEARGVHPADCMMDLLLEEDGQVPIVYFHMSDDDVRQVIGYSRSLIASDSLTCETGMPHPRLYGTFPRVFAKYVREERVLTLEDAVRKLTSFPVQRFRLGKRGLIVPDYAADLVVFDPDTIRDTATYSEPKQQPEGISTVVVAGRIAMQDGAHTGARGGGFLRASSCACGHGHAHGGAGR
>NZ_CP045802.1|WP_153782628.1|409709_410852_+|amino-acid-aldolase
MEMERNEAAVGAGERLADGIDTPCVVIRSEAVDANIAAMAAEAARRGVQLRPHVKTHKLPELAHRQVAAGACGITAAKLSEAEAMADGGIGDIFVAYPVVGAVKARRAAELARRVRLLVGVDSLAGARQLSAAAEAAGLALEVRLEIESGLQRTGVPPEAALALAREIAAMPGLSLTGIFTYRGAMLGGAPTLDLRAAGHEEGRLMAGVAETLRRGGIAIRDVSVGSTPTAIYAAEIDGVTEIRPGTYVFQDRMQTAFGVCRPEDCAAEVWATVVSRPAPDRIVIDGGSKTFATDVQPDKPPLHLQGFGRVIGLPHAVFERMNEEHGVIRISPDDTCEPGDMLRIVPNHICSTVNLHGSVYVSGKSGLRRVPVAARGCIQ
>NZ_CP045802.1|WP_153782627.1|409072_409726_+|transcriptional-regulator
MQTVSAMLPMLTELAQGIAAQFGERCEVVIHDWSRPYDSTIVFIANGQVTGRKVGDPGTNLGLEVMRGTSEGGHRQNYVTRTKDGRLLRSTSIYLKDDEGQGIGALCINLDISELMAAEKALQGLIGLQELPPVRESFVSNVSDLLDSLIQEAEDAVGCPPALMGREDRIRFIALLDRKGAFLIKKAGEKVCAYLGISKYTLYSDLEEAKGSDGDGA
>NZ_CP045802.1|WP_028599361.1|408294_408762_-|VOC-family-protein
MIEGLYEAHLPVSNLERSRAFYAGLGLRQAWEDEDTVFFWIEEGKSWIGLWLAPELAALPYHPAIRHAAFRVDWEGLLRSAAWLKARGIEPAPFGRQPDAAPFVRPHQANASIYFDDPDGNSLELMCSVEVPADWREHAGKIPAADWPPGNGGTA
>NZ_CP045802.1|WP_153782626.1|407893_408298_-|hypothetical-protein
MKRAAAWLLPLLIFAAGSAAAAWLLIGPPASGDGWAAIGKAAPDEAASARKRAVLAAYAGLTPEESRLLPASPKDSAVLAMTAGPELAQRIGAEHEGRTVHAVRFRVIGPGDAGTLTVYLSQDGKTVLGKERAR
>NZ_CP045802.1|WP_153782637.1|418136_419534_+|hypothetical-protein
MKKASAFLAAMLLASALGGTAFAANEAKSGTTLKTSVEVSGSKTTTDAIIADGVLYVPIRSVAAATGYKTEWDSAKKEVRLDTLASGQTAKAVDRIAPAQQLELKRLDIAFYLDGKLTALVDADGKAVQPLFQQDTLFLPMRALADALGLTASWNAKEKKLTLGKAGDASGSTAVVPVKGDKGDTGAQGSKGDKGDAGAQGPAGPAGAKGDQGDKGDKGDKGDKGDKGDKGDAGAAGSSGATGAQGSKGDKGDAGAQGPAGPAGAKGDKGDTGAQGPAGPAGPKGDQGDIGATGPAGATGPQGAAGPQGAMGPVGPQGAQGDPGPAGTGYLPSMSAYNTIPEDRIILDSNGNNIRFTQLTSTPNSSIAADISSGRFTIDSSGYYYLSYSIRSNQTRAANSRILVNQLEIPEFSNLNQSSQSRWQASGLIRLNAGDVVSLQLFGSIAGSVDLDGGQGASLTLIRVF
>NZ_CP045802.1|WP_028599369.1|419754_420441_+|response-regulator-transcription-factor
MRIHVLVADDDPHIRELLRLVLTREGYAVAEAADGEQAAAVLEREQVHLAVVDVMMPHKDGLQLTEEIRRHYDLPVILLTAKGEMADKEKGYSAGTDDYLVKPFEPQELLFRIRALLRRYRIASSETIALGRVVIDRQSYEVTAGRETLTLPLREFQLLSQLASQPGRIHTREQLISLIWGADYEGDSRTVDVHIKRLRERFEAYRDDFTIVTIRGLGYKLEPGGRRG
>NZ_CP045802.1|WP_153782638.1|420437_422123_+|HAMP-domain-containing-protein
MRTLYFRIVFIFVLIALASGLGGLAVTSFYYEAKLKSGSEHAMEEASRQVRELDALAGAERREQTLQAVSGLSYQLYVVRPDGSAQTYGAAFRHGFLPPEKAVREVRSGGIYPGMTEEDRRFKLLAYFENSPRNTYGFPLPRPDGGIDAVFIRPDLESQIGEVRIILAVLLASTFGLSLLLIAALSRLIVAPVKRLTRAVQRMAAGDYDVRVDTARRDEIGELGRRFTAMAGAVRQLDRMRQEFVANVSHEFQSPLTSIRGFIRTLLDGAAAARDEEARRYLTIIDEESRRLSSMSRQLLLLADVDRPDRALDRRSFRLDEQLRQAILLLEWQWTFKELELDLELPERTVFADEGLLYEIWLNLLGNAIKFSPQGGVIGVSLRVLENGRDGSADMDHPLAEGTGRPAGRSQERRDNRKATAGRWLEVVIADEGPGIPPEELPHIFERFHKADRARTWQAGGMTEHSSAGPHREGFAPEDSSAGVLAEGGGAPRRDLRPLSPGGGQASPPSGAGSGLGLSIAQRIARLHGGDIEALSEPGQGAAFRVTLPEGGAQGREGGGA
>NZ_CP045802.1|WP_153782639.1|422343_422616_+|hypothetical-protein
MLGLLGLALAALWMDHVHRDGRQEAVTVLKAIEGEELVFASEDGEDLRAEAPQLLLPLLEVGREYRIVVDRNRFRHAVLQKIEPHDASSK
>NZ_CP045802.1|WP_153782640.1|422569_423361_+|PH-domain-containing-protein
MRCFRRSSLTTLRRNSGRSSRSRQRCGRPARMKRVKRGRTSIRRGADMEQDQRQPERSIVTGGAAPAPEPMSAAAGQAQERPDGEAGAGGGGQVERPFATDGEPSSSEPLRPLDLRVIRARRLEGAVTSGVYAAVVLALALLSARFGWPWWIAAGAGALALAGAALELLWLPRLLHRSWGYLVREHEIELAHGFIVRKRTLVPVARIQHIDTKQGPIQKRCGIATLTMATAAGSHAIPGLPEEQAEAMRSRLAELTRRADDEI
>NZ_CP045802.1|WP_153782642.1|423350_425063_+|PH-domain-containing-protein
MRSEAASAELRRVHPASMLFFLAKGVKEMYGMLPLLPLLVLWVPRATGLDVSRVGLGALLGGVGLSALLAAAWLRWRRFGYAAEAGAIRIEQGVWSRRTIWIQRERIQSVDTRQNLAERALGLVQLRIETAGGGEKAEAVLPSLSAAEAARLQRLLGFAEAGAAEPEESAAGVGAGAEAVRQAAAPEARRDIGADGLEREAGAVLAASDAARQPEPTFDAAASAASAAAAASAAGRRTELTVGQRKIRPGDLLGYALTSYRTGLVFLLLAGLLSRAADSGWLRRLDVQAELEQLFGDYVLAVAGLLLLLAAWLLTALQLLNANWGFRLERRGRKLHVERGLLEKKRQTIDIARIQALELAQPLLHRPLGWMAVRAFIAGNAEEKERHLLLFPVLKRAEAEAFLREFAPAFVLPADWSRLERSAWTAYAGWPALASLLPAAAGWIWIPEPYRWLAALLPAAVLAYGLLEHRHAAWALEAGQLSLRRGALIRSELLLPGRRIQWHRMSLSPMQRRRGRASLSVSIATGKGARSFRLCHAPAAAVERLLRQLSWRPGRGSGSPAAVRSAPQSE
>NZ_CP045802.1|WP_153782643.1|426915_428754_-|SgrR-family-transcriptional-regulator
MYAAERYLSLLERFSGVAAEGSPVEATLDGIAAALFCTPRNAKLILRRMQEEGLIEWLPGRGRGHRSRIVFLRPKEPYLMELLQAEAEAGNYPAAFELIGRHAGGTSAKERFLEWLDGRFGYRKEQQQGQPSRDTLRFPLLYGVRTFDPSQLNYALDAHVMRQLYDRLLQYSEESERIVPAAAHHWSVNGEGTVWTFFLRKGVLFHDGADLTSRDVAFTFERLRHGPNRWLMRSVRSVEAVGTHVVRFHLHQPNFIFDRFVCAGAASLLPEGLRGLPEEEFWRRPIGTGPFRLLKHTSCGLELGAHEPYYGGRPYLDAVDMVVLPEGCQPVKVAPSVPGLLRIRDGFFNEPETAPPSEGWSSIHNVNHGCAMLGWNMNKPGPHQSEAFRRAVRMILDPSELLDELKDKSVLPAYGFLPETSALRSPEPPRPDRLRAALREAEYDGTPIRLTTVAKYKDEVDWAARKLAEWGIRVETKLEAITSKHGFREADLTVWCIVIAEDEVCEIEAYEHGDCILGNYLTDDTRSWIRGRIDAALATPDAVGRRQIMRQVEEQLRDDGSLIFLHHQQLSTYLHPSVHGVRLNRLGWVDFKNVWLENGLAAPELTASELRP
>NZ_CP045802.1|WP_153782644.1|428880_429057_+|hypothetical-protein
MLEDQYVSEKLEQFRQEERRNVSGKGALLGKLGARAFRRWSRINRTGDEEHDGGSILG
>NZ_CP045802.1|WP_146000487.1|429031_429220_+|hypothetical-protein
MMEDQYLAEKLEQFRQEKYRRMERQGRWRLELEKDEAPAGRSGRSRLGRALAAIASLLAMRR
>NZ_CP045802.1|WP_052333351.1|429569_430778_+|peptidase-S8
MMDWQWLPAVLLLPAAAGVWWMAGQAGAWLAERSMPEHEPGEMLVKFAEGLAAEGRHRIHRRCGCEAVEELGRTGLHVVRSVRGRASARKLKALYERHPGVEFAEPNYVYRTCLVPGDPYYSLQHGPKQIGAERAWEKTRGDRRIIIAVLDTGIDSSHPDLADKVLPGKDFVDPAGTGEDGNGHGTHVAGIAAAEADNGIGIAGIAPGVSLLPVRVLDAAGNGTLRRIAAGIRYAADQGAHVINLSLGGPARSSALRAAIRYAVAKGAVVVAAAGNTGSSDPVYPGAYDEVIAVGSVDPQDLPSAFSAYGPWVELAAPGERIASTYAGGRYTYFSGTSMAAPHVAGTAALLASLGLTGEQIRARLLETADRSGDGGLCWSCGRVDAGQAVAGGGEGGTDGAA

Crispr_ID: NZ_CP045802_3

• CRISPR_ID: NZ_CP045802_3
• CRISPR_location: 512806-512878
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_3

Consensus_repeat	Method
CCAACGACTCCTCAGACGCTTAG	CRISPRCasFinder

spacers of NZ_CP045802_3

>3.1|512829|27|NZ_CP045802|CRISPRCasFinder
CCGCCCTTTTTTCGCGTCTCCAAAAAT

CRISPR arrays and Neighbor proteins around NZ_CP045802_3

CRISPR arrays

The CRISPR arrays of NZ_CP045802_3

>merge|NZ_CP045802|3|512806-512878|CRISPRCasFinder
CCAACGACTCCTCAGACGCTTAGCCGCCCTTTTTTCGCGTCTCCAAAAATCGAACGACTCCTCAGACGCTTAG

>NZ_CP045802|3|1|512806-512878|CRISPRCasFinder
CCAACGACTCCTCAGACGCTTAG	CCGCCCTTTTTTCGCGTCTCCAAAAAT
CGAACGACTCCTCAGACGCTTAG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_028599421.1|504378_505341_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP045802.1|WP_153782687.1|519258_520158_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223472
NZ_CP045802.1|WP_028599426.1|509336_510587_-|copper-amine-oxidase-N-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|377924
NZ_CP045802.1|WP_043111471.1|518329_519241_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_CP045802.1|WP_153782689.1|520318_521968_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270299
NZ_CP045802.1|WP_153782685.1|515811_518046_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|227095
NZ_CP045802.1|WP_028599422.1|505342_506161_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP045802.1|WP_153782690.1|522094_523006_-|DUF4097-family-beta-strand-repeat-protein	unknown	unknown	gnl|CDD|372574
NZ_CP045802.1|WP_028599425.1|509049_509268_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028599428.1|511164_511374_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028599438.1|524169_525540_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270452
NZ_CP045802.1|WP_028599427.1|510608_511016_-|hypothetical-protein	unknown	unknown	gnl|CDD|319906
NZ_CP045802.1|WP_043111516.1|507129_508929_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224055
NZ_CP045802.1|WP_127464475.1|506344_506884_+|copper-amine-oxidase-N-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|377924
NZ_CP045802.1|WP_084137384.1|513257_514277_-|1,4-dihydroxy-6-naphthoate-synthase	unknown	unknown	gnl|CDD|270353
NZ_CP045802.1|WP_084137383.1|511488_512655_-|cation-transporter	unknown	unknown	gnl|CDD|224151
NZ_CP045802.1|WP_028599436.1|523002_523563_-|DUF1700-domain-containing-protein	unknown	unknown	gnl|CDD|285278
NZ_CP045802.1|WP_153782683.1|514273_515002_-|futalosine-hydrolase	unknown	unknown	gnl|CDD|350166
NZ_CP045802.1|WP_028599420.1|503063_504320_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270450
NZ_CP045802.1|WP_153782691.1|523559_523880_-|PadR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224609

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_028599421.1|504378_505341_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	3.5552e-77
NZ_CP045802.1|WP_028599426.1|509336_510587_-|copper-amine-oxidase-N-terminal-domain-containing-protein	gnl|CDD|377924	pfam07833, Cu_amine_oxidN1, Copper amine oxidase N-terminal domain. Copper amine oxidases catalyze the oxidative deamination of primary amines to the corresponding aldehydes, while reducing molecular oxygen to hydrogen peroxide. These enzymes are dimers of identical subunits, each comprising four domains. The N-terminal domain, which is absent in some amine oxidases, consists of a five-stranded antiparallel beta sheet twisted around an alpha helix. The D1 domains from the two subunits comprise the 'stalk' of the mushroom-shaped dimer, and interact with each other but do not pack tightly against each other.	9.33658e-13
NZ_CP045802.1|WP_043111471.1|518329_519241_+|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	2.33751e-120
NZ_CP045802.1|WP_153782689.1|520318_521968_+|extracellular-solute-binding-protein	gnl|CDD|270299	cd13581, PBP2_AlgQ_like_2, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	6.64878e-167
NZ_CP045802.1|WP_153782685.1|515811_518046_+|helix-turn-helix-domain-containing-protein	gnl|CDD|227095	COG4753, COG4753, Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain [Signal transduction mechanisms].	2.30884e-23
NZ_CP045802.1|WP_028599422.1|505342_506161_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	4.48849e-71
NZ_CP045802.1|WP_153782690.1|522094_523006_-|DUF4097-family-beta-strand-repeat-protein	gnl|CDD|372574	pfam13349, DUF4097, Putative adhesin. This has a putative all-beta structure with a twenty-residue repeat with a highly conserved repeating GD, gly-asp, motif. It may form part of a bacterial adhesin.	1.37761e-26
NZ_CP045802.1|WP_153782687.1|519258_520158_+|ABC-transporter-permease-subunit	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	3.26374e-60
NZ_CP045802.1|WP_028599438.1|524169_525540_+|extracellular-solute-binding-protein	gnl|CDD|270452	cd14749, PBP2_XBP1_like, The periplasmic-binding component of ABC transport systems specific for xylo-oligosaccharides; possesses type 2 periplasmic binding fold. This group represents the periplasmic component of an ABC transport system XBP1 that shows preference for xylo-oligosaccharides in the order of xylotriose > xylobiose > xylotetraose. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	8.81961e-110
NZ_CP045802.1|WP_028599427.1|510608_511016_-|hypothetical-protein	gnl|CDD|319906	cd07242, VOC_BsYqjT, vicinal oxygen chelate (VOC) family protein similar to Bacillus subtilis YqjT. 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.	1.53215e-44
NZ_CP045802.1|WP_043111516.1|507129_508929_+|ABC-transporter-ATP-binding-protein	gnl|CDD|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	3.90009e-137
NZ_CP045802.1|WP_127464475.1|506344_506884_+|copper-amine-oxidase-N-terminal-domain-containing-protein	gnl|CDD|377924	pfam07833, Cu_amine_oxidN1, Copper amine oxidase N-terminal domain. Copper amine oxidases catalyze the oxidative deamination of primary amines to the corresponding aldehydes, while reducing molecular oxygen to hydrogen peroxide. These enzymes are dimers of identical subunits, each comprising four domains. The N-terminal domain, which is absent in some amine oxidases, consists of a five-stranded antiparallel beta sheet twisted around an alpha helix. The D1 domains from the two subunits comprise the 'stalk' of the mushroom-shaped dimer, and interact with each other but do not pack tightly against each other.	5.81313e-22
NZ_CP045802.1|WP_084137384.1|513257_514277_-|1,4-dihydroxy-6-naphthoate-synthase	gnl|CDD|270353	cd13635, PBP2_Ttha1568_Mqnd, A menaquinone biosynthetic enzyme exhibits the type 2 periplasmic-binding protein fold. This group includes Ttha1568 (MqnD) from Thermus thermophilies HB8, an enzyme within an alternative menaquinone biosynthetic pathway that catalyzes the conversion of cyclic de-hypoxanthine futalosine to 1,4-dihydroxy-6-naphthoate. Menaquinone (MK; vitamin K) is an essential lipid-soluble carrier that shuttles electrons between membrane-bound protein complexes in the electron transport chain. Ttha1568 has significant structural homology with the members of type 2 periplasmic-binding fold protein superfamily. The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	3.30098e-81
NZ_CP045802.1|WP_084137383.1|511488_512655_-|cation-transporter	gnl|CDD|224151	COG1230, CzcD, Co/Zn/Cd efflux system component [Inorganic ion transport and metabolism].	1.20228e-106
NZ_CP045802.1|WP_028599436.1|523002_523563_-|DUF1700-domain-containing-protein	gnl|CDD|285278	pfam08006, DUF1700, Protein of unknown function (DUF1700). This family contains many hypothetical bacterial proteins and putative membrane proteins.	1.00779e-48
NZ_CP045802.1|WP_153782683.1|514273_515002_-|futalosine-hydrolase	gnl|CDD|350166	cd17766, futalosine_nucleosidase_MqnB, futalosine nucleosidase which catalyzes the hydrolysis of futalosine to dehypoxanthinylfutalosine and a hypoxanthine base; similar to Thermus thermophiles MqnB. Futalosine nucleosidase (MqnB, EC 3.2.2.26, also known as futalosine hydrolase) functions in an alternative menaquinone biosynthetic pathway (the futalosine pathway) which operates in some bacteria, including Streptomyces coelicolor and Thermus thermophiles. This domain model belongs to the PNP_UDP_1 superfamily which includes members which accept a range of purine nucleosides as well as the pyrimidine nucleoside uridine. PNP_UDP_1 includes phosphorolytic nucleosidases, such as purine nucleoside phosphorylase (PNPs, EC. 2.4.2.1), uridine phosphorylase (UP, EC 2.4.2.3), and 5'-deoxy-5'-methylthioadenosine phosphorylase (MTAP, EC 2.4.2.28), and hydrolytic nucleosidases, such as AMP nucleosidase (AMN, EC 3.2.2.4), and 5'-methylthioadenosine/S-adenosylhomocysteine (MTA/SAH) nucleosidase (MTAN, EC 3.2.2.16). Superfamily members have different physiologically relevant quaternary structures: hexameric such as the trimer-of-dimers arrangement of Shewanella oneidensis MR-1 UP, homotrimeric such as human PNP and Escherichia coli PNPII (XapA), homohexomeric (with some evidence for co-existence of a trimeric form) such as E. coli PNPI (DeoD), or homodimeric such as human and Trypanosoma brucei UP. The PNP_UDP_2 (nucleoside phosphorylase-II family) is a different structural family.	2.53072e-74
NZ_CP045802.1|WP_028599420.1|503063_504320_+|extracellular-solute-binding-protein	gnl|CDD|270450	cd14747, PBP2_MalE, Maltose-binding protein MalE; possesses type 2 periplasmic binding fold. This group includes the periplasmic maltose-binding component of an ABC transport system from the phytopathogen Xanthomonas citri and its related bacterial proteins. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	5.1209e-38
NZ_CP045802.1|WP_153782691.1|523559_523880_-|PadR-family-transcriptional-regulator	gnl|CDD|224609	COG1695, COG1695, Predicted transcriptional regulators [Transcription].	8.81605e-22

Protein sequences

>NZ_CP045802.1|WP_084137383.1|511488_512655_-|cation-transporter
MSHEPDLRRRVGKDTPPFESTRSLGQAEPGQTHNHDHLSRSHDGHSHARSAHSRSHDGHSHSHSGHSHSGNGHSHSHAGHSHSHNHGHSHAGHGHFHGGGSGNKRGLLIALLITTGIMVLEFVGGLATGSLALLSDSGHMLSDAGALLLSLVAVGFAARPSSPKRTFGFRRFEILAALFNGATLIAIAIFIVVEAWGRFWEPPTVASRSMLLIAAVGLLANLASAWFLMRQGDVKGNVNLKSAYLHVLGDALGSVGAIAAGALMWAFGWYWADPAISVLVSLLIVKSAWGMLRSTVHILMEGAPETVDTQRVQLELESLPGVIDVHDLHIWTITSGFDAMTCHLLVEDDADSRRVLQQAIALLRDGHGIRHCTIQIEDSSVRHEELGC
>NZ_CP045802.1|WP_028599428.1|511164_511374_+|hypothetical-protein
MDLEREVQDLKRRVEELEERELATSERGYGPVGRRDTGLGGKFLIGIGIGAAVLVLLLFTIGVIQFIRV
>NZ_CP045802.1|WP_028599427.1|510608_511016_-|hypothetical-protein
MLHHIELYVSDLQKSASFWGWFLGELGYEPFQEWPEGRSWKHGSTYLVFVQAKEKYLDVPYHRARVGLNHLAFHAASREQVDRLTDEVRARGMNLLYEDRHPHAGGAGTYILFFEDPDRIKVELVAPAEEQRLPE
>NZ_CP045802.1|WP_028599426.1|509336_510587_-|copper-amine-oxidase-N-terminal-domain-containing-protein
MKPVRHAHAKAPLGTRRAGRSALGMLLAVLLLSGSATTPAAAAEPAGSQAPAAAVKPTASPTPATSFKELAASCGPSTLKSVLIGGASGVDDQLYGARKEDAARIKKVCGMVQAFAKKGKPVKAFDSTPYSFFYGLSLTFSNKGDASIFGSTGGLYLESGSTFLQLDDISVSKDYSSLFVRNEEIAEIPATARFGEKIRLKGHDPLLFSPELFVYWTPNAETYSSSSDSSGYPYDHSLLIGTGTQQFGYYDFSITLPAYGKAKDGTMKFLESKGSLSLYVAYGGNGSRTLGEMSLLPAAEPFLSVDGKPALDAALRPILREGRALLPLRSIAKLAGKSVVWDKASWSALIRSEPPAPRKGAYSFPQLWIDGKLAAPELQPILRDGLTYVPIRALTAAFGISVSWNAASRSVDIELP
>NZ_CP045802.1|WP_028599425.1|509049_509268_-|hypothetical-protein
MAYIRPLHTDADFQEALDERIPVRVFRDDHMVESGSCIVRFDERTVVLQSGVADLAYHARAQCEFFELRKKS
>NZ_CP045802.1|WP_043111516.1|507129_508929_+|ABC-transporter-ATP-binding-protein
MNRTAPAPISSASFESAFQQAATTENRTAFQYLMSLYKGNFLNLTISIVFFLVKSLPVYVLPIVTANMINIVAQPDQHSLRELWINFAVLIAVVLQNIPTHAAYVSFLSRAIRSVEAGLRGAMVRKLQQLSINSHRELAAGRLQSKVLRDVEAVEGMSKQLMLAFIPAIFNVVIAFGLTLYSNWLVSLFYVLTVPAAIGVMQMFKRRIRQSNREFRKEIETMSSHVSEMVEMIPVTKAHGLEQVEIDRIDTTLRRLQGKGYRMDLVEAYFGASGWVTFQIVQVVCLLFTAYLAYTGSIPVGNIVMYQGYFGMILGSITALINVYPMIAKGTESISSITEILRSTDIEDNAGKLKLTRLSGEYRFEDVQLKFPDGDQHVLEEVSLDVRAGECIAFVGESGAGKSTILNLVIGFLNPTSGRVLVDGVPLSALDLSEYRRHLAVVPQTNILFSGSIRDNITYGLQGITEEQVMEAVERAHLTEMVSRLPKGIDTMVGEHGGKLSGGQRQRIAIARALVRDPSVILLDEATSALDNASEHHVQQAMQQLIQGRTTFIVAHRLSTIRHADRIVVMKRGRIAEVGTFDELIARKGEFYNLKQLQM
>NZ_CP045802.1|WP_127464475.1|506344_506884_+|copper-amine-oxidase-N-terminal-domain-containing-protein
MTKQPFRGNRVYSFENMILILKGLRKLSRRIQVLFLALIVGLSVFGAGLAGAAKAPSNNDGIHRPAIVINGKVAELKAVIPPSGSAMVPFRSFFEALDLNAEFDNKTKTVTAKNETTTVTLTAGKMTGTINGKEIKLIQGPSLSDDDDLMYVNVRFIAEAFGGIVGFDKSTLTVTLDFD
>NZ_CP045802.1|WP_028599422.1|505342_506161_+|carbohydrate-ABC-transporter-permease
MKARSILLHVGLTAGLLLSVFPFYWLLVMATRTTADIYSFPPKLWFGTKLGDNVSRVFENIDFFGAFWNTLFVATACAALVLFFDSLAGFTFAKFEFPGKKILFVLLLATMMAPAQLSLVPSFVIMAKLGWVGSFKALIIPGMANAFGIFWIRQYAQESVPSELLDAGRIDGCGFFRLYWNVALPILRPALSFLGAFTFIGAWNDYLWPLIILTDESKYTLQVALASLNGIYLSDYSMVIAGTLLAVIPLIVLFLFVSKQFISDIAAGAIKS
>NZ_CP045802.1|WP_028599421.1|504378_505341_+|sugar-ABC-transporter-permease
MGKPMLNPEPARVPSSRRTEGGLAARIWKHRKEYLAISPFYILFAVFGLFPIAFSMYLSFQKWDGIGRMSYNGLNNYRFMLTDPEFWRAVGNTLLIWIYSTIPMLFLALVVAFLLHSSFVRMRTLYRVGYFLPNVTSLVAVAIVFGTIFSNNYGLLNYTLNLLGLNSIEWLNRTWGIQLAISVMVIWRWAGYNAIIYLAGLQSIPTVLYEAAKIDGASGVQAFFRITVPNLRPIILFTLITSTIGGMQVFTEPQVLVGNDGGAGGGGLTIVLYLYREAFVHNYFGYGAAVGWGMFILIALFSIVNWLFVQGRPSHDQGVK
>NZ_CP045802.1|WP_028599420.1|503063_504320_+|extracellular-solute-binding-protein
MVKFRRIGLPLLSLALVAAGCGGPAPAENTKTLTLWYWNRSLDDGLIQSVEQKFPGIKINAQKIGGDFKSKLKTTLAAGTDGPDIVAFNDWVSELFVSSDRFYDLYELGAKEIEPDFLDWKWNFGVTAEGTMIALPIDTGPTALFYRADLFAEAGLPSEPADVQRELGTWESYLQAGRQLQDHFGGKVKLLDNVKNIYTQFNAQSDRIYFSTDGEFIGDKPESSVKKAWDLAVQAARMKLAGNADAFTSEWNAAMNNGSIASFVGAVWMKEILEQGAPDTAGKWRVARAPGGDGNNGGSFLAIMKSSRYPKEAFDVIRYLQSPDNQIRTYKNINLFPSAAKALDDPILQEKEPFFGDQATGQIFAESARGVKPAYFGDKFTNVNGIALRELNSVALQGKDPDKAWRDALSRIRKELLR
>NZ_CP045802.1|WP_084137384.1|513257_514277_-|1,4-dihydroxy-6-naphthoate-synthase
MKMKIAYSPCPNDTFVFHAWAHGLIAGAPELDVTYADIDVTNGWAARGEGPEVMKISYAALPYVLDRYALIPCGGALGRGCGPLVLTAGGGRIAAERAEVGGAAEPTAGTDRREAGDAAASSQGGSGAAARPSADASAGAARSHVGAAAPGMDPSWLSGRTVAVPSDRSTAYLLFRLWTAQQITGEPPRIVVLPFHEIMPAVRDGRVDAGLVIHEARFTYPDYGLTLMADMGVWWEADTGLPIPLGAIIARRGMDVESLARWTRASVEYAWAHPDESAGYVREHAQEMSPDVARSHIALYVNEFTRSLGEDGLAAVESLLGRAAREGLVPDFDPALLRS
>NZ_CP045802.1|WP_153782683.1|514273_515002_-|futalosine-hydrolase
MKKRILPDPPAYVLIVAAVEAERDAVVRGLMKACPEESCGEAEGPLRRVGRYIVVAGGVGPAAAAASTALAIAGGPPLRYVVSAGIGGGFPGAAPIGSVVVATEIVCADLGAETAQGFASVDELGFGSWRVKTDREVAEALAEALRQAGMAATAAPVLTLSTVTGSGETAAELLRRVPGAAAEAMEGYGAALAASMHGIEAMEVRAISNAVGPRDRDAWRIGDALAALERTAAILPEVLNIR
>NZ_CP045802.1|WP_153782685.1|515811_518046_+|helix-turn-helix-domain-containing-protein
MAEGRIFMKSSWFRKLLLSYLPAFFIVVSILFVVFFQALNEQSRKEAAKANDFLVQQAIRHADNSLRAIDYRILQDILGSAVLKDFYRAEAEDVFVNLQADRLMDSWAFGNPAIDSIYLYRPRDGFVFGDGSLKTEPFRDAAFLRSYLDGERPIGQWSDKRSFQPYAMSKPAEVMTIVRAYPGFSSVKTGYVVVNVSLSKLGQELASMYDPGQTFIAMSDRSGQPAIGPRLDGGELVLAQYVSPYTGWTVSSGPTGKGLKLTLDLYSVWLVLALGAVLLGIAWVVHVTRRNYRPISQLVSLIRSSSLVPQDGPGADRNELGFIRLSLEQLMEEMKRSKQQDTENRLLRKRHRFLEALAGGAPISQAEWESDLERLGFEPRGRTAFAWTLEIDRHAAFCRAYTAHDQAMLKFVLASVVTETVQGGGGAAWAEWTGDRRMSAIVWLPPEAGLDEARRLAAEASDWIRDNLAFGATMALHGPAGPLEEIRRSADIAASLLAYKAALGTGEVITPDRLGSGGSPLHDHFGTIQQLAQAFRTGDPGWRERLRSLYAQIRQSCFSRQEIESLQQVLYQQMDRMFLELAKEYWTAWKEAEAELLALDREWEALDELEAGCLGALERMDARMSELRDSQSARSEIAQIRAYMEENFGSPELSLDYFGDRFSIHPKTISKLFKEQFGENFIDFLMGLRMEQAKRMLGEPSLSLQEISRHIGYYNYNSFNRAFKNHTGMSPSDFRKRAPRPSAG
>NZ_CP045802.1|WP_043111471.1|518329_519241_+|sugar-ABC-transporter-permease
MPMAHAWTRVKRSWELYVLLLLPVLYLIVFKYVPMFGVLIAFKDFNIVQGILGSPWVGLKHFEALFRSPNFPILIQNTLLISLYSLAAGFPVPILLALALNEVRTGLFKRSVQLVTYAPHFISTVVMVSILILMLSPHVGIADRLYGLFGWTAPNFMGEPGFFKSIYVWSGVWQEMGYASIIYMAALAGVDPSLYEAARMDGASRLRKMLHIDLPALVPITVILLILSLGNIMGVGFEKIYLMQNPLNVATSEVIATYVYKVGLLGANFSFSSAVGLFNSVINLILLVAVNTISRRVSQNSLW
>NZ_CP045802.1|WP_153782687.1|519258_520158_+|ABC-transporter-permease-subunit
MLRSRRIKEPIGDRMLVAAIYAALALVAVAVAYPLLYIVSSSFSSPRAVVSGQVWLLPVDFSLRAYASIFQSSQLMLGYWNSIVYTVVGTFLNVAFTVLMAFPLSQRRLAGRGFFMVLMMTTMFFSGGLIPTYLLVKELHLLDTRWAMWLPRVFSVFQVIVARTFFQTSIPAELQEAAEIDGCRDIRYLWSVVLPLSKPILAVLTLMYAVGHWNAYFDALIYLRSEHLFPLQYVLRNLLILNASDPEMLANTTKGMRDQGFEQALKYALIVVASVPVLVLYPFVQKHFAKGVMVGSLKG
>NZ_CP045802.1|WP_153782689.1|520318_521968_+|extracellular-solute-binding-protein
MGWKREGKRLAVLLAATGLLLGACSSGSENGAAGGEAAGAAEDGKPVEMTFFAVQGKAPLEENEYTKRVEEKFGVKIKWDLAPQDALKDRRQLLLASGDYPEVFLEGKFSNTDLLTYSKQGVLIPLNGLIDQYAPNLKALMEKKPYLKESMTAPDGNIYGIPRFNECYHCTYSEKYWMNKDWLDKLGLQVPTTTDELYEVLRAFKTKDPNGNGKADEIPLTGAPNKNVWNGNFDAYLMNAFIYNDNDKYLTLQDGQVGFAADKPEWREGLAYMRKLYKEGLIDPAAFTQNDQAISQLGNREGDEIVGSMTTALLSYLVNVWDDGITRHQHWVAVPPLKGPGGVQLTGVQQGITDFAFALTNKASERQQIAAIQLVDYAFSEEGALLSEYGVQEGIGWNKAKEGELNIWGKPAKYSFDNLPPADENEIRNDSWSLLGPKDMSKEFRDAFASSQNPLSSKGYETRLAQATKLYEPYAPAEFYPSGAYLRPEDTETAAQLTTGIKEYVMTNLAQFVIGNKDLDTDWDAYVKGFDGLNLKQYIDIYQAAIEKK
>NZ_CP045802.1|WP_153782690.1|522094_523006_-|DUF4097-family-beta-strand-repeat-protein
MNRSMRNVVLLGLILLLGGLIGAGVTFGQGDRESLLQFGTEEVRLSEEVPADGISRLRAEAGSMDIELAAGASDDKIVATITGRASKKSLDKIKLELDPQGDELTVKGKEGGVFTFGFNIVNVTMRIEVPARKFEALQAELGSGDIDAQGVEAGELTFKTGSGDIELSGVKGGVISLRSGSGSIDGEGVVAEELAAKASSGNISLEDVLAALQLDAGSGNIRAEMDRLELPVTASSGSGNITLATRVAPASATVQYSVGSGRFRSDWNEDEDGERKSRELVFGDGQVQVKLSTGSGNISLREE
>NZ_CP045802.1|WP_028599436.1|523002_523563_-|DUF1700-domain-containing-protein
MTREHYLNELWQQLAPVPEAKRREWMYDYEEHFRIAAEQGQPEEQTAAELGDPRAVARELLLGYRVEAASQGGGGVRLVSRAVFAAVGLGFFNLVFVLGPYLALLGLLLALWAVAGSFVIAAFAVLLEGWTGDAIAMPLAVFGAMIAGGLGLLLGAAAYKLTGGIMRLTLKYLLANTKMMKRSVAR
>NZ_CP045802.1|WP_153782691.1|523559_523880_-|PadR-family-transcriptional-regulator
MNVQFKKGVLDLCVLSLTAWEDRYGYELAVAMSSKFEVAVGSVYPLLNRLTQEGYFTTYLRESPEGPPRKYYKLTPLGHQHLMELVREWRTFSHAVDELIKEGVER
>NZ_CP045802.1|WP_028599438.1|524169_525540_+|extracellular-solute-binding-protein
MRRSEKKALKKSALLLTAGALAVGLAACGSGNEPAANTGGASNEAAANTGASGGDSGKKVTITFQNIYPDETSVTNKIMKELVADYEAANPNIKIELDSLNTDQQKLKLKTQAASKEVPDITIVNPAAQMKPFVDAGVLAPLNDMLDQNGLKDTFQKGLLDYYSFDGNVYALPDGNNIEVVYYNKDLFAQAGITDVPKTFDEMLEDVKALKAKGITPIAIGEKDTWTGSFLFMNILLRTNGGPGFLQDVMDGKKDFNDPAFTEAVDAFQELVQAGAFPEGATSIDANAGGNIFKTGKAAMFIIGSWETGNIDASSVAGKVGAFSFPTVNGKGDVNQFMLAPGSGFAISANSKHPQETKDFLNYFMTNFPKKKFELKDAVGLGQVVEGDFAAAGYSDLAVGILDLFKSVSGGDLAFDNTMNPAVAQAHLSSIQNLFVQKVDSKQVAKEHQDAFAANK

Crispr_ID: NZ_CP045802_4

• CRISPR_ID: NZ_CP045802_4
• CRISPR_location: 544441-544513
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_4

Consensus_repeat	Method
CTAACGATACGGAGAAACGCTAT	CRISPRCasFinder

spacers of NZ_CP045802_4

>4.1|544464|27|NZ_CP045802|CRISPRCasFinder
TTTGCCTATATCCGCGTTTTCCGAAAG

CRISPR arrays and Neighbor proteins around NZ_CP045802_4

CRISPR arrays

The CRISPR arrays of NZ_CP045802_4

>merge|NZ_CP045802|4|544441-544513|CRISPRCasFinder
CTAACGATACGGAGAAACGCTATTTTGCCTATATCCGCGTTTTCCGAAAGCTAACGATACGGAGAAGCGCTAT

>NZ_CP045802|4|2|544441-544513|CRISPRCasFinder
CTAACGATACGGAGAAACGCTAT	TTTGCCTATATCCGCGTTTTCCGAAAG
CTAACGATACGGAGAAGCGCTAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_153782697.1|538717_540733_-|iron-chelate-uptake-ABC-transporter-family-permease-subunit	unknown	unknown	gnl|CDD|236720
NZ_CP045802.1|WP_028599447.1|536088_537060_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|185037
NZ_CP045802.1|WP_028597989.1|560352_561291_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_CP045802.1|WP_153782695.1|537132_537327_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028597991.1|556972_558301_-|glycoside-hydrolase-family-125-protein	unknown	unknown	gnl|CDD|377716
NZ_CP045802.1|WP_028599451.1|541858_542116_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153782700.1|547392_547878_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_CP045802.1|WP_153782698.1|540729_541731_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|238566
NZ_CP045802.1|WP_153784640.1|551242_552166_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|227095
NZ_CP045802.1|WP_028599453.1|542555_543260_-|hypothetical-protein	unknown	unknown	gnl|CDD|224755
NZ_CP045802.1|WP_127464474.1|543713_543995_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153782701.1|548000_548648_+|nitroreductase-family-protein	unknown	unknown	gnl|CDD|380314
NZ_CP045802.1|WP_153782702.1|549018_549576_+|translation-initiation-factor-IF-3	unknown	unknown	gnl|CDD|234582
NZ_CP045802.1|WP_028599452.1|542136_542433_-|hypothetical-protein	unknown	unknown	gnl|CDD|375079
NZ_CP045802.1|WP_153782703.1|554004_556746_-|alpha-mannosidase	unknown	unknown	gnl|CDD|223460
NZ_CP045802.1|WP_028597993.1|552436_553804_+|MATE-family-efflux-transporter	unknown	unknown	gnl|CDD|240539
NZ_CP045802.1|WP_153782696.1|537578_538607_+|acetylesterase	unknown	unknown	gnl|CDD|368448
NZ_CP045802.1|WP_101808449.1|558470_559403_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP045802.1|WP_028599454.1|543383_543608_-|PspC-domain-containing-protein	unknown	unknown	gnl|CDD|224894
NZ_CP045802.1|WP_153782699.1|544895_547247_-|AAA-family-ATPase	unknown	unknown	gnl|CDD|223288

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_153782697.1|538717_540733_-|iron-chelate-uptake-ABC-transporter-family-permease-subunit	gnl|CDD|236720	PRK10577, PRK10577, Fe(3+)-hydroxamate ABC transporter permease FhuB.	2.60854e-175
NZ_CP045802.1|WP_028599452.1|542136_542433_-|hypothetical-protein	gnl|CDD|375079	pfam17247, DUF5316, Family of unknown function (DUF5316). This is a family of unknown function mainly found in Firmicutes. Might contain multiple trans-membrane sequences.	1.10518e-06
NZ_CP045802.1|WP_028597989.1|560352_561291_-|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	9.12737e-132
NZ_CP045802.1|WP_028599447.1|536088_537060_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|185037	PRK15079, PRK15079, oligopeptide ABC transporter ATP-binding protein OppF; Provisional.	1.30349e-153
NZ_CP045802.1|WP_153782702.1|549018_549576_+|translation-initiation-factor-IF-3	gnl|CDD|234582	PRK00028, infC, translation initiation factor IF-3; Reviewed.	2.57882e-28
NZ_CP045802.1|WP_028597991.1|556972_558301_-|glycoside-hydrolase-family-125-protein	gnl|CDD|377716	pfam06824, Glyco_hydro_125, Metal-independent alpha-mannosidase (GH125). This family, which contains bacterial and fungal glycoside hydrolases, is also known as GH125. They function as metal-independent alpha-mannosidases, with specificity for alpha-1,6-linked non-reducing terminal mannose residues. Structurally this family is part of the 6 hairpin glycosidase superfamily.	0
NZ_CP045802.1|WP_153782700.1|547392_547878_+|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	1.72243e-16
NZ_CP045802.1|WP_153782698.1|540729_541731_-|ABC-transporter-substrate-binding-protein	gnl|CDD|238566	cd01146, FhuD, Fe3+-siderophore binding domain FhuD. These proteins have been shown to function as initial receptors in ABC transport of Fe3+-siderophores in many eubacterial species. They belong to the TroA-like superfamily of helical backbone metal receptor proteins that share a distinct fold and ligand binding mechanism. A typical TroA-like protein is comprised of two globular subdomains connected by a long alpha helix and binds its specific ligands in the cleft between these domains.	1.43405e-72
NZ_CP045802.1|WP_153784640.1|551242_552166_-|helix-turn-helix-domain-containing-protein	gnl|CDD|227095	COG4753, COG4753, Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain [Signal transduction mechanisms].	2.78337e-22
NZ_CP045802.1|WP_028599453.1|542555_543260_-|hypothetical-protein	gnl|CDD|224755	COG1842, PspA, Phage shock protein A (IM30), suppresses sigma54-dependent transcription [Transcription / Signal transduction mechanisms].	7.98089e-18
NZ_CP045802.1|WP_153782701.1|548000_548648_+|nitroreductase-family-protein	gnl|CDD|380314	cd02137, MhqN-like, nitroreductase family protein similar to the NAD(P)H nitroreductase MhqN. A diverse subfamily of the nitroreductase family containing uncharacterized proteins; includes nitroreductases MhqN, YodC, YdgI, DrgA. Nitroreductase catalyzes the reduction of nitroaromatic compounds such as nitrotoluenes, nitrofurans and nitroimidazoles. This process requires NAD(P)H as electron donor in an obligatory two-electron transfer and uses FMN as cofactor. The enzyme is typically a homodimer.	7.00096e-57
NZ_CP045802.1|WP_101808449.1|558470_559403_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	2.7967e-70
NZ_CP045802.1|WP_153782703.1|554004_556746_-|alpha-mannosidase	gnl|CDD|223460	COG0383, AMS1, Alpha-mannosidase [Carbohydrate transport and metabolism].	0
NZ_CP045802.1|WP_028597993.1|552436_553804_+|MATE-family-efflux-transporter	gnl|CDD|240539	cd13134, MATE_like_8, Uncharacterized subfamily of the multidrug and toxic compound extrusion (MATE) proteins. The integral membrane proteins from the MATE family are involved in exporting metabolites across the cell membrane and are responsible for multidrug resistance (MDR) in many bacteria and animals. A number of family members are involved in the synthesis of peptidoglycan components in bacteria.	5.72532e-159
NZ_CP045802.1|WP_153782696.1|537578_538607_+|acetylesterase	gnl|CDD|368448	pfam05448, AXE1, Acetyl xylan esterase (AXE1). This family consists of several bacterial acetyl xylan esterase proteins. Acetyl xylan esterases are enzymes that hydrolyze the ester linkages of the acetyl groups in position 2 and/or 3 of the xylose moieties of natural acetylated xylan from hardwood. These enzymes are one of the accessory enzymes which are part of the xylanolytic system, together with xylanases, beta-xylosidases, alpha-arabinofuranosidases and methylglucuronidases; these are all required for the complete hydrolysis of xylan.	6.9255e-75
NZ_CP045802.1|WP_028599454.1|543383_543608_-|PspC-domain-containing-protein	gnl|CDD|224894	COG1983, PspC, Putative stress-responsive transcriptional regulator [Transcription / Signal transduction mechanisms].	4.29436e-18
NZ_CP045802.1|WP_153782699.1|544895_547247_-|AAA-family-ATPase	gnl|CDD|223288	COG0210, UvrD, Superfamily I DNA and RNA helicases [DNA replication, recombination, and repair].	9.50042e-137

Protein sequences

>NZ_CP045802.1|WP_127464474.1|543713_543995_+|hypothetical-protein
MESDLDPGPGSARAEVVRGRNRMKSCRRAQAIGASPLSTKEVPILMGKNKASKADVQSTKLNSFAANQDTEFAQDLTADAKAAFGSVNKKKKK
>NZ_CP045802.1|WP_028599454.1|543383_543608_-|PspC-domain-containing-protein
MKTLYRSRTDRKIAGLCGGIGRTYGFDPGLVRIGFIAVGVFSCGTALLLYAAASVVLPKEPEWNGPPPREPFYS
>NZ_CP045802.1|WP_028599453.1|542555_543260_-|hypothetical-protein
MSVFDRILNLTKATANEMLNKMENPTLMMNQYIRNMEEEIDGMKSELHRQQAASRSYGSRLEEVTQLAQHNQAKAEEALREGREAEARAALEAKLRYSDQEQEYRRLHEQAKHASVELEIRLDSAKEELQRLIQKRNELSERIQKAEAAAERTAPSFSHGFEPGRASRGFERIEEKVLQWEAQLGLSRDYKGPSASSSSYAGGYEAAPSAAPDNGRSAAIDEQLADLRRKMKGE
>NZ_CP045802.1|WP_028599452.1|542136_542433_-|hypothetical-protein
MTRITLVFLSAGLGLAAVAGAVGLVAGQDSLVRISAWSGGIPLLLAMLFSGAFIQADSRRIGTYTDDGESLRRRNDWSARCLLLAVPSLLLCAGAYFL
>NZ_CP045802.1|WP_028599451.1|541858_542116_-|hypothetical-protein
MTMRRFLASLVFLSTNIFLAAYALDIKQLPGPAWVNDAADVAYVLGQALVLLLAEVRRPPAEKALRLYSLVSLVMLVVFASVKLA
>NZ_CP045802.1|WP_153782698.1|540729_541731_-|ABC-transporter-substrate-binding-protein
MKRLLSGTTALLAVLLLTAACGSTTTENTGSAATSSPAPSSAETAGPIVIKHGKGETKLDKPAEKVVALEWIYSEELIALGIQPVGNADNKEYKLYVTDEAALADSVTDVGLRWEPNLETIASLKPDLIISNTDNNDAIYDQLQAIAPTIEFDPYPNEGDAYTGMVNDFKTIAQAVGKSKEAEQVLADLDAHYAEAKQKLADAGKDNFHYVITQAFTSQNAAALRMFTDTSTVVQTLDRIGLINDWKSEEFEKYGFTDATFESLPAVSGSNFIYIVQDNDNVFGESAKDNKVWNSLDFVKENRTYGIGGDTWTFGGPLSSKALVDRVVDAITK
>NZ_CP045802.1|WP_153782697.1|538717_540733_-|iron-chelate-uptake-ABC-transporter-family-permease-subunit
MRTSILFGGGAAALFLLLIASLCFGEAQITVHVVADALLHRQDALEHHIIWDMRLPRAILGVLSGAGLAVAGALLQTATKNPLASTDTLGINAGAYFMVVAGTVYFPTLLHQSPFLFAAAGGGLAALCAYVLGGGRAATPIRLALSGMIVAMVIGSFTSALHIFHATETQSLFLWGSGSLAQLDWHGVAYAWPGVVAVVLIAFFMSRQFDVLNLDPSTARSLGQKVELARFAGLTLAVLAASVVVSVAGPIGFVGLVAPHLVRLSGLSKHSGLLPAAALWGAVLLTGADVLARIVRSSMGEMPVGAMMAIIGAPWLIWLILRKMNGALGSPPSSPMSIGSGRVPIRFPLLAAIMLAAVVSFILVSMTMGGTRIPLGQLFASLIGSEQAGSYSVLLNLRLPRTLVAAGAGIALSVSGVLIQASVRNPLADSSILGVTSGAGFGALLVLIAWPESPIFLLPIAAVGGAAAAAAIIFLFAWRKSLSPAVLILLGIAVSAVGSAGIQALIVLGPLWGSTGYIWLTGSTYGRTWTQVGVIALFLAVLLPVAVRLSRKFDVLAFSDDSAAGLGLPVRKTRLAAMTTGVLLAAGAVAVAGTVGFLGLIVPHMVRSLIGHNTRRSILLSSLIGALLMVMADAVGRTILAPVEIPSGLFITLIGAPYFLFLMFRSQTRKI
>NZ_CP045802.1|WP_153782696.1|537578_538607_+|acetylesterase
MMNSYASIPGNTELNHLQRRKMELQLYMPPLTMEKEKSEAFWQPRLKQAWSKPLRETRKRVDEELFPYADVYRITYEGYDETPVSGLYMVPAQAAREGRQVPCIVIYPGYTAGAGYPEDHAGWLLAGYAVLAVDARGQGGETGSLLPSLHGMAKGWMTQNLLEGPDRTYYMALFVDSLKALQAAASQPEADARRLVPCGGSQGGGLALAVAALCGLEAPAGIGLAAVLADIPNLCHVDQAIFSSAGSLSEAGQLASRKPEELSRLLEHLACFDNMNLACRISAPVLASVGWKDPICPPETVYAAYNRIHAPKEIRDYPFLGHEVNGAHRRDKLQFVLEHAGR
>NZ_CP045802.1|WP_153782695.1|537132_537327_-|hypothetical-protein
MMADDLYRYELELKRHHRQSGQAAGGPRLPGQAAPPNPLVRPGGVRLGTMSHGAGRALLSWLRS
>NZ_CP045802.1|WP_028599447.1|536088_537060_+|ATP-binding-cassette-domain-containing-protein
MASQPNAMLEVDNLSKFFEVGKGKTLKAVNGLSLSIRKGETLGMVGESGCGKSTAGRTIMRLYEPTSGQVRYNGSNIYDLKGSKLKAFRREMQMVFQDPYASLNPRWTVENIIAEPLDIHKLVSSPKERKVAVERLLDKVGLNPSHLTRYPHEFSGGQRQRIGIARALAVDPKFIVADEPISALDVSIQAQVVNLLQNLQRAEGLTYLFIAHDLAMVKHISDRIAVMYLGKLVEIADSEDLYADPRHPYTQALLSSIPIPDPEIEANKERIVLRGDLPSPISPPSGCPFRTRCPAATERCAAEVPELRQVGPNPSHWAACHYA
>NZ_CP045802.1|WP_153782699.1|544895_547247_-|AAA-family-ATPase
MLKGTTNRHSPAGAPFATGETCPMSANLPLPFKKPFGAAGRGLPAAALASGENSRRLVPDDDADSGFFRALESRGLFLNGPQIEAVRHGAGPLLTLAGAGSGKTSVLAARTGYLIAERGADPRSILLVTFSVKAAQEMKDRISALPGIAPAAAKAVTARTFHSFFLQLLRSQGYRQEILGGGPLAVIVLKGMLRELGIADRLEPETALAALSEAKLSLRPLGELPEASQAERDLKRLLLRFEEWKEREGRMDFDDILLWSHRLLTERPALLRTLQERFRLIMIDEFQDTSRLQYELIRLLAGKRANLMAVGDDDQTIYGFSGARSEYILGFRDAFPGARVVTLDTNYRSSASIVGLGNDIIRHNKARYAKTLKAVRTSRQVPLYIRPFTTDQEAAAVAAHIRERVDEGARGWGDFAILYRTASNSRAMFEQLVLSDIPFHLQDSGELFYDQSAVRPLVDYLRLSIKRRDFAAMEGVLPSMYVGRAKGMAHIRAKDDPRPKKGPLIHLLTLDGLKDFQRDSIQARITFIKGLKALKPADAIRRMRKDFYDAWLDAEAAGAGGADTVYKETLREALDELEASAGRFADVPSFLAFVKRIGERHAEMRALPPEAARDAVKLMTIHKSKGLEFPAVVLIGASEGILPHSLALEADKLSDYGNGAAATGDTASLREAALEEERRLAYVAVTRARDELLVSSPSLWRGRKTDVSRFLLDAFRTAAPAAAAAGGAAHAAAGRGVGVSAAAEASPAARRANLGAATSAAAAAAAAAAGRAKADRPQAWPKA
>NZ_CP045802.1|WP_153782700.1|547392_547878_+|MarR-family-transcriptional-regulator
MSCRTEDLLYVLIHLNKQLACRFETDVGVSPNRLELLCQLRGAEEISQSELQKAVSIDPAAVTRHMQQLEAEGKLVRTRCQDDNRVTKVRLTDEGRSWIESCNRQKERFMERLQAGLEESERKELLRLLAALGRSLEEPPLPAALPAALRLRRSGARRARG
>NZ_CP045802.1|WP_153782701.1|548000_548648_+|nitroreductase-family-protein
MTNAAAVVRTNDYREIVAGRRSVREYDPTVKISREEMTELLEEATLAPSSVNLQPWRFVVVESEEAKAALAEIAPRNRTQVITSAAVIAVFGDMQAFDYAGDIMASSVAKGYMTQEVMDQMLANYGALFGSVPKEAFRDMILLDTGLVSMQIMLAARARGYDTNPIGGYDKSRAAETFGLEADRYVPSMLISIGKAAKDARLTTRLPVDRVAEWK
>NZ_CP045802.1|WP_153782702.1|549018_549576_+|translation-initiation-factor-IF-3
MAVLINEQIKAFEVELTGLGGERLGVVERAEALELARAAGADLVCTSLMSSPPPCRLMPKGKGKAAAQQEAAAARRSAAPTGAGGKPGAGGKGGAAAKGGADKAKELRFTAHIEEHDYETKLRQADKHLRSGKPVQLVVKASGAKEAAAAKAVLERLLADLKEAGVKETGVQSSGKGSQVRVNPK
>NZ_CP045802.1|WP_153784640.1|551242_552166_-|helix-turn-helix-domain-containing-protein
MKLLQFALPPLPYYIASGHEDHPPGMVHVDRCNIGLFDLLAVEEGELLVTEGDRSYEVGPGQALILRPDAHHYGTAPTRLRTRCYWLHFKHDGYWTATDERLPLYRDPRGEWIGRDVFAGEEPDNAHDAEWKMNAPLFSVQMPQYADLVEPARMFELLGQLTAMTSSGQVGGALWRQQILFQELLQQLSAGLDARSTSPSAACAAQAAAYLRQHYREDISARAMSESLNFHSVYIARCMQKEFGCSPKEYLLRYRIDQSKLLLLRTDYPVSRIAGDVGFNQAAYFASCFAKYEGLSPRSYRQRFSHA
>NZ_CP045802.1|WP_028597993.1|552436_553804_+|MATE-family-efflux-transporter
MKNRNYSLWALSWPIFIELFLQFLLGAADTFMVSEISDDAVAVVGFSHQLFNALTVLFTVIASGAGILIAQKLGARKEEDARSISIIALKTTVLIGAAISVLLIALPGPIASLLQMPEELLPLARTYISIVGGSMILAAIMSTLSAAIRNTGNTRGPMYTAIGMNVVHIFLNYGFIYGAFGLPEWGLAGVAISTVVSRLLASALLVYMFLFAFERRIWWGDIKLWSRSLFREILRIGWPLGVYSGNWVLSQLVIFTFIGTLGAAQLAARTYMNTLESFCFLIGFSIALATQIRVAHLFGAGNTREAYKDAYKGLWIGQLVVIANSFIIFLFGSQALGLFTSDPDILAICAGLLGLNLLLQPGKMLNMTIADSLNAVGDTRFTMYVSTISMWGVAVLVSYFFSIHLGYGLTAIYICMIADEYLRGFVCWLRWRSFKWASRAGSPELPAQGAAAAEA
>NZ_CP045802.1|WP_153782703.1|554004_556746_-|alpha-mannosidase
MTKRTAHILSHTHWDREWYLPYEKHHVRLVQLMDSLLDTLETDPGYRSFFLDGQTIILDDYLEVRPENRSRLEKLIREGRIGIGPWYILQDAFLTSGEANVRNLQIGHEEAGRWGPVSKIGYFPDTFGLFGQTPQLMRQAGIDNALFGRGVKPTGFNNEVGESSAYESSFSELVWEGPDGSRVLGILFANWYSNGNEVPTDEEQARAYWERKLADAGRYASTPHLLFMNGCDHQPIQTDLAEAIRVAGAVEPDVEFVHSNFPDYLDAVRAAADGSALSVVRGELRSQLTDGWGTLVNTASSRVYLKQLNAAGQSVLERSAEPLAAYARLVGKDYPQHLLAYAWKLLLQNHPHDSICGCSVDEVHREMVTRFDKSRHVAETIVADSAAFVAEAVDTSVFGSYGADALPFVVFNPSGWMRSGTVSVELDAARIYFRDGVGFGEMNRRMKELDLSGRALVGADGRTLACKVEDLGLQFGYDLPDDAFRQPYQCRRVRLTFQADAVPALGHATYAWVRSDVRPETAPDIAADARTLDNGVLRVEVAEDGSFALTDRRTGQTFPGLGIYEDSGDIGNEYMFMAPKGVEPLTTRGVPAAVSVVENGPGRASLEIVHEWAVPASADETLDREQREIVYYPQRQAGRSAKLVPLRLRTVLSLEQGSGRIDIVSSFDNQARDHRVRLLFPTGLQADTHTADSIFEAAVRSTEPAPEWENPSNAQHQQAFADVSGQAANGSAAGLTVANVGLCEYEVLRDGRNTIAVTLLRSTGELGDWGYFPTPEAQCIGPHEARLALVPHGGDGAASGAFAEAYQLQTPWTAVQTGVHVGKLAAVGSPLAWEGESIAFSAFKASPVTGDLVVRLYNLKREPASLRLLAPAGASSAYKSGVLEQETADALELRDGRLELAVGPAEIVTIGLR
>NZ_CP045802.1|WP_028597991.1|556972_558301_-|glycoside-hydrolase-family-125-protein
MEQFRLPAIPMPELKLPAAVRQALDDAEAKLAGRPKLQRLFRNCFPNTLETTTKLMPDGTTFVITGDIPAMWLRDSVEQVIHYVPLAKDDAGLQRILEGLIRRHMAMILIDPYANAFNESANDWHWNTTDETDMGPWVWERKFELDSICFSFRLAYAYWQETKHTAIFDTDFKRAMRAAIDLWKREQRHFEQSPYRFVRDNGIPEDSLRNKGLGMPVNYTGMIWSGFRPSDDACDFHYNIPANMFAVVTMRQMQEIAEWVFRDMALVKELADLAAEVEHGIRLYGIFRHPQFGPIYAYETDGYGNHCLMDDAGTPGLMSIPYFGYAAADDPIYLNTRRFALSSENPYYFEGKQAKGIGSPHTPDGYIWHMALSMQGLTAISDEEKLAMIDLLEATDADTGYMHEGFHSDDPSVFTRKWFAWSNSLFAQLVWRAMQDGLIGRG
>NZ_CP045802.1|WP_101808449.1|558470_559403_-|carbohydrate-ABC-transporter-permease
MSKPSAALPPKAARDFHKLSPAWNAAFHAVAGLFALLCVFPFVFIIIISFTNEQALAADGYRLIPAEWSLEAYRYVLQNGDALLRSYGVTIFVTVVGTALGLLVVTLYAYGISRKSFQYRKFFNFFAFFTMLFNGGLVPTYIVVTQMLGLKDNVWALILPLMVNAFYVLIMRTFFMTMVPDAIIESGKIDGASELQIFYKLVLPLALPGLATIALFSTLGYWNDWFNALLYIENPNLVPLQSMLMRIETNMQFLLSQASSNASLAQGLQNMPQDTARMAMVVLATGPIVLAYPFFQRYFVQGLTIGAVKE
>NZ_CP045802.1|WP_028597989.1|560352_561291_-|sugar-ABC-transporter-permease
MNGLAGFFRSLNRNKAILLMVLPGALWFLIFSYIPMAGAVIAFKEYRVSRHGFIDSVISSAWVGLDNFKFLFSTNDAWIITRNTLLYNVVFIVIGLVAAVAMAIVLSEIASKRMSKLYQTGMFMPYFLSWVIVGYFAFSFLSLDKGLLNQALRGIGLDPVNWYSDPTYWPFILVFISLWKAIGYNSVVYLASILGIDRSLYEAAMIDGANKWQQIKNITIPMLTPLMTILTLLAIGKIFYADFGLFYQVPRDSGALYSVTNVIDTYVYRGLKTTGEFGMVTAAGLYQSLVGFILVITSNWIVGRVNKDNTLF

Crispr_ID: NZ_CP045802_5

• CRISPR_ID: NZ_CP045802_5
• CRISPR_location: 828370-828469
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_5

Consensus_repeat	Method
CAGGCGCCTCGCCTAGCGCTCAGCCC	CRISPRCasFinder

spacers of NZ_CP045802_5

>5.1|828396|48|NZ_CP045802|CRISPRCasFinder
TCGAGCAGCGCGGCATCGCCCTCGGCGATTCGGCCCTCGCCCGGCCCA

CRISPR arrays and Neighbor proteins around NZ_CP045802_5

CRISPR arrays

The CRISPR arrays of NZ_CP045802_5

>merge|NZ_CP045802|5|828370-828469|CRISPRCasFinder
CAGGCGCCTCGCCTAGCGCTCAGCCCTCGAGCAGCGCGGCATCGCCCTCGGCGATTCGGCCCTCGCCCGGCCCACAGGCGCCCCGCCTAGCGCTCAGCCC

>NZ_CP045802|5|3|828370-828469|CRISPRCasFinder
CAGGCGCCTCGCCTAGCGCTCAGCCC	TCGAGCAGCGCGGCATCGCCCTCGGCGATTCGGCCCTCGCCCGGCCCA
CAGGCGCCCCGCCTAGCGCTCAGCCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_101809403.1|831863_833615_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_CP045802.1|WP_153782779.1|829202_830441_-|MFS-transporter	unknown	unknown	gnl|CDD|340882
NZ_CP045802.1|WP_052333495.1|820933_821587_-|phosphatase-PAP2-family-protein	unknown	unknown	gnl|CDD|239486
NZ_CP045802.1|WP_127464481.1|816484_819532_-|response-regulator	unknown	unknown	gnl|CDD|236848
NZ_CP045802.1|WP_028600087.1|840144_840522_+|hypothetical-protein	unknown	unknown	gnl|CDD|377776
NZ_CP045802.1|WP_028600083.1|835393_836686_+|carbohydrate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_CP045802.1|WP_153782778.1|828487_829228_-|MOSC-domain-containing-protein	unknown	unknown	gnl|CDD|225758
NZ_CP045802.1|WP_153782777.1|821789_822551_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028600080.1|830623_831571_+|ribose-phosphate-pyrophosphokinase	unknown	unknown	gnl|CDD|234929
NZ_CP045802.1|WP_101808516.1|822814_824554_-|M20/M25/M40-family-metallo-hydrolase	unknown	unknown	gnl|CDD|236208
NZ_CP045802.1|WP_101808520.1|827514_827886_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028600085.1|837800_838640_+|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP045802.1|WP_101808523.1|833589_835242_+|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_CP045802.1|WP_052333494.1|820007_820718_-|lysoplasmalogenase	unknown	unknown	gnl|CDD|377946
NZ_CP045802.1|WP_052333493.1|815235_816465_-|hybrid-sensor-histidine-kinase/response-regulator	unknown	unknown	gnl|CDD|236848
NZ_CP045802.1|WP_101808519.1|827002_827497_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028600084.1|836891_837797_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP045802.1|WP_101808518.1|825264_826794_-|long-chain-fatty-acid--CoA-ligase	unknown	unknown	gnl|CDD|236072
NZ_CP045802.1|WP_153782780.1|838737_839988_+|GDSL-family-lipase	unknown	unknown	gnl|CDD|238859
NZ_CP045802.1|WP_101808517.1|824492_825008_-|ATPase	unknown	unknown	gnl|CDD|176868

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_028600085.1|837800_838640_+|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.69007e-83
NZ_CP045802.1|WP_153782779.1|829202_830441_-|MFS-transporter	gnl|CDD|340882	cd17324, MFS_NepI_like, Purine ribonucleoside efflux pump NepI and similar transporters of the Major Facilitator Superfamily. This family is composed of purine efflux pumps such as Escherichia coli NepI and Bacillus subtilis PbuE, sugar efflux transporters such as Corynebacterium glutamicum arabinose efflux permease, multidrug resistance (MDR) transporters such as Streptomyces lividans chloramphenicol resistance protein (CmlR), and similar proteins. NepI and PbuE are involved in the efflux of purine ribonucleosides such as guanosine, adenosine and inosine, as well as purine bases like guanine, adenine, and hypoxanthine, and purine base analogs. They play a role in the maintenance of cellular purine base pools, as well as in protecting the cells and conferring resistance against toxic purine base analogs such as 6-mercaptopurine. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. The NepI-like 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.	7.04201e-72
NZ_CP045802.1|WP_052333494.1|820007_820718_-|lysoplasmalogenase	gnl|CDD|377946	pfam07947, YhhN, YhhN family. The members of this family are similar to the hypothetical protein yhhN expressed by E. coli. Many are annotated as possible transmembrane proteins, and in fact they all have a high proportion of hydrophobic residues. A human member of this family, formerly known as TMEM86B, is a lysoplasmalogenase that catalyzes the hydrolysis of the vinyl ether bond of lysoplasmalogen. Putative conserved active site residues have been proposed for the YhhN family.	1.00984e-30
NZ_CP045802.1|WP_127464481.1|816484_819532_-|response-regulator	gnl|CDD|236848	PRK11107, PRK11107, hybrid sensory histidine kinase BarA; Provisional.	6.59375e-53
NZ_CP045802.1|WP_028600087.1|840144_840522_+|hypothetical-protein	gnl|CDD|377776	pfam07100, ASRT, Anabaena sensory rhodopsin transducer. The family of bacterial Anabaena sensory rhodopsin transducers are likely to bind sugars or related metabolites. The entire protein is comprised of a single globular domain with an eight-stranded beta-sandwich fold. There are a few characteristics which define this beta-sandwich fold as being distinct from other so-named folds, and these are: 1) a well conserved tryptophan, usually following a polar residue, present at the start of the first strand; this tryptophan appears to be central to a hydrophobic interaction required to hold the two beta-sheets of the sandwich together, and 2) a nearly absolutely conserved asparagine located at the end of the second beta-strand, that hydrogen bonds with the backbone carbonyls of the residues 2 and 4 positions downstream from it, thereby stabilizing the characteristic tight turn between strands 2 and 3 of the structure.	1.72827e-59
NZ_CP045802.1|WP_028600083.1|835393_836686_+|carbohydrate-ABC-transporter-substrate-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	6.07905e-48
NZ_CP045802.1|WP_153782778.1|828487_829228_-|MOSC-domain-containing-protein	gnl|CDD|225758	COG3217, COG3217, Uncharacterized Fe-S protein [General function prediction only].	3.93476e-30
NZ_CP045802.1|WP_028600084.1|836891_837797_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	2.56176e-71
NZ_CP045802.1|WP_028600080.1|830623_831571_+|ribose-phosphate-pyrophosphokinase	gnl|CDD|234929	PRK01259, PRK01259, ribose-phosphate diphosphokinase.	5.58054e-136
NZ_CP045802.1|WP_101808516.1|822814_824554_-|M20/M25/M40-family-metallo-hydrolase	gnl|CDD|236208	PRK08262, PRK08262, M20 family peptidase.	0
NZ_CP045802.1|WP_101808517.1|824492_825008_-|ATPase	gnl|CDD|176868	cd07826, SRPBCC_CalC_Aha1-like_9, Putative hydrophobic ligand-binding SRPBCC domain of an uncharacterized subgroup of CalC- and Aha1-like proteins. SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain of a functionally uncharacterized subgroup of CalC- and Aha1-like proteins. This group shows similarity to the SRPBCC domains of Micromonospora echinospora CalC (a protein which confers resistance to enediynes) and human Aha1 (one of several co-chaperones which regulate the dimeric chaperone Hsp90), and belongs to the SRPBCC domain superfamily of proteins that bind hydrophobic ligands. SRPBCC domains have a deep hydrophobic ligand-binding pocket and they bind diverse ligands.	6.83956e-34
NZ_CP045802.1|WP_101808523.1|833589_835242_+|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.60191e-56
NZ_CP045802.1|WP_052333495.1|820933_821587_-|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.	2.83582e-37
NZ_CP045802.1|WP_052333493.1|815235_816465_-|hybrid-sensor-histidine-kinase/response-regulator	gnl|CDD|236848	PRK11107, PRK11107, hybrid sensory histidine kinase BarA; Provisional.	4.44159e-64
NZ_CP045802.1|WP_101809403.1|831863_833615_+|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	4.96695e-68
NZ_CP045802.1|WP_153782780.1|838737_839988_+|GDSL-family-lipase	gnl|CDD|238859	cd01821, Rhamnogalacturan_acetylesterase_like, Rhamnogalacturan_acetylesterase_like subgroup of SGNH-hydrolases. Rhamnogalacturan acetylesterase removes acetyl esters from rhamnogalacturonan substrates, and renders them susceptible to degradation by rhamnogalacturonases. Rhamnogalacturonans are highly branched regions in pectic polysaccharides, consisting of repeating -(1,2)-L-Rha-(1,4)-D-GalUA disaccharide units, with many rhamnose residues substituted by neutral oligosaccharides such as arabinans, galactans and arabinogalactans. Extracellular enzymes participating in the degradation of plant cell wall polymers, such as Rhamnogalacturonan acetylesterase, would typically be found in saprophytic and plant pathogenic fungi and bacteria.	8.10481e-94
NZ_CP045802.1|WP_101808518.1|825264_826794_-|long-chain-fatty-acid--CoA-ligase	gnl|CDD|236072	PRK07656, PRK07656, long-chain-fatty-acid--CoA ligase; Validated.	0

Protein sequences

>NZ_CP045802.1|WP_101808520.1|827514_827886_-|hypothetical-protein
MKPVQASQTYPRLTVYSEERYGGVSRIYRGNLGIRDTDRILDGFESLRFFSTSPNATLVVFSETRFRGNFRVYRGSVRNLPDLDDLIGGEDVESLISTNQSLTDAQIREIRRTGSLPAGYRLL
>NZ_CP045802.1|WP_101808519.1|827002_827497_+|hypothetical-protein
MELYFRDNFFSSGETEIMDASGRPIGKVDLRSAFGSSLEIFGAAGESLYEGRFLAFSSKWRVLQAGGEEIGQLRWRMAFFSKRFEYDSYGRGVYQLTSPAMSKEYEIADEDGRIVGRFERVSGWMSAGAFRLECGECQVPPLEWAAVILGMNAMQKQSAAAGGV
>NZ_CP045802.1|WP_101808518.1|825264_826794_-|long-chain-fatty-acid--CoA-ligase
MSWNLVEALENSAASFPEREAYVYRGASATYAELIEQVRRCAAGLAAEGIAKGDKVVLLLGNAPEFIASLYGALALGAIVVPVNPTYTADELAYILADSGARAAIAAAPLRPLLAALQARLPRPIQPFYVGEEEGEDSFARLLQLGAGHLESAYIDEEDTAVILYTSGTTGKPKGAMLSHRNLATNAESVYTMFELTENERAVAVLPMFHIYSLTVCLNAPLAVGACIVILPRFHPVETIAAIREQRATMFSGVPTMYAYLLQVPDATAADFATLRLCSSGGASLPVEMLRKVEERFGVVIYEGYGLSEAAPVTAFNPLGGKRKPGSVGVDIPRVTNRIVDHQGNEVPRGEIGELIVQGPNVMQGYYKLPDATAEALRGGWLHTGDIARMDEEGYIYIVDRMKDMINVGGFNVYPREVEEVLYRHPGVFEAAVVGVPDETLGEAVKAYVVRSDEALTAEELAAFCSGSLVKYKRPTAIEFLAELPKNSSGKTLRRALKEKAQQPPSAQA
>NZ_CP045802.1|WP_101808517.1|824492_825008_-|ATPase
MTTSMRIRVEGNQFIMERTFGAPKDLVFRAFTEAEHLKKWWGPRGWTLTRCDIDFRPGGVWHYCMKCEDPAQGDFYGMESWGKTIYKETNPQDFYSCTDYFSDEEGTINEELPPCFTELEFVERDGSTTVINRSRYETAAQLQSVIDMGMEHGVRETWDRLEEHLAAVQSA
>NZ_CP045802.1|WP_101808516.1|822814_824554_-|M20/M25/M40-family-metallo-hydrolase
MASAKHGTGSRSIWPPFNPPEPDGPRRTGCRRPPAAMRLRPGPDPTSDSGRHAGGIRSSSGRECYPLTRGGGIGTVDLYSPNLSPMQRRRSPMPQPAVSILLLLLALLLVLAAVLLVRAARFRPDAADLAPHAGGGEPIPVDADAAAGRLSQLIRKRTVSSREPSSADRAEFRSLLDLLPDLYPAAHRALEREIVNGRTLLYRWQGAEPEAPTVLMSHFDVVPAEEEGWLHPPFSGEIADGRVWGRGAIDTKGTLVCILEAVEQLVASGFKPKRDIYLSFCDDEEIAGDGAPTHVRLLQERGIRPGLVVDEGGAVVENIFPGVRGPIAVVGVAEKGVSDFELVVRGAGGHASAPPRLGPAFRLARAIQRLERRPPKPFFPPPTLDMLDTLGRRSSFGYRILFANLWLLRPLLARLFHRLSPETRALSSTTIAVTTLQGSPAANVLPAEAKAGANVRVAVGETAAGVAARMRRAIADDAVELRIVRAGDPSPVSTTREEPYRIVAAAIRGTYPEAAVTPYVMLGGSDSRHFAAVWPYVYRFTPYELSREERETIHAANESLPIRKLGKGIEFYIRLIRSV
>NZ_CP045802.1|WP_153782777.1|821789_822551_+|hypothetical-protein
MSTDPQNRPIPADLREEEERPPSYGRSAPPFAAEHEAAASLAAQGASAKGMGGAAAARLKQVDGRRLAALLRDPLQGLREEPERDSAYGWIGLGASVLGFLVWTLFMQKALQGLFYSLFGFGGLFAYEPGFDFGLALRMLLGGALSLAALLGSLYLFGSRFGSRKRSLLQAAVPLGAMQLLSGAGFAAAGIAALASIRLSLLLLVVTLLVTLATTVTGTAELFEVRQERRFAFIAASIASYAVVLLVLFSLLF
>NZ_CP045802.1|WP_052333495.1|820933_821587_-|phosphatase-PAP2-family-protein
MKAWLIAAAAALAFAALALWAPMDGTAPIDDSIRGSWSLTAEEQPAAAMEALNKLGSTAVFAGATLLAAALSWAFGRRRQAVVVIGTVLAALLLNSGLKEWLQRPRPEHAGWIEASGYSFPSGNAMVGMALYGLLAVIAWRGARSGWLRLAAAAAAVLVIGAVGYCRLYFGVHYATDIAAGYAAGLFCAAAGAALLGPGGSRSSALRRRGSHPTFPG
>NZ_CP045802.1|WP_052333494.1|820007_820718_-|lysoplasmalogenase
MPTPKLDPKSPAEPKSASRLVLPLLIALMGLIYIFAVPFEPEALKLTFKLVPMALIFAYAWTRLPKPADRRPWQTLGLIGLVFCAVGDGTLRWFVIGLSAFLIGHLFYLSSFLLRMRFSPLRIAALLPLAAYGIFMGMRLVEALRGSGQTGLIVPVIAYVAVISLMAWSAIQTGDRQAIAGSLLFVASDSILSWNLFVADVPFSHALIMLTYYGAQFLIAGSLSSRGSDAAPALRR
>NZ_CP045802.1|WP_127464481.1|816484_819532_-|response-regulator
MRAGLAETAGIAERIERGEPVASAAADAPADELGAIAGSFRQIARSLHVKTEQERTLRLQAEEEAWLNARVSEMAILLQGSIEVGAASRIFLAKLASSVDASCGALYALRPDGAYHAAAGYAHDEAELPSEPVRLGQGLVGQCAENRAMIELAEVPPGYIRVRSGLGAAEPAALLLVPILYEDKAVAVLELASFRGFSGKERQLIGRVGADMGILINTLADVARIDELLRETQLQKEELESQTEELQVQAEELQLQTEELQAQTEELKAQTDQLHRQSLDLEASNEQLRLQAEELRGQTEQLEASNRSLLAQTELSERQKLEIQAQAEEILLAAQHKSEFLANVSHELRTPLNSLLILSQILAENRPGNLVGKQLEYIHTIYSSGKDLLQLIDEILDLAKLETGKMTPVIEPTELQDIAGRLYRMFEQQAQSKELAFDIRIAPDAPDSIDTDGHRAQQILRNLLSNALKFTDEGSVALSIRKGAAAADEVVFEVEDTGIGVPTAKLESIFEAFQQADGTTSRKYGGTGLGLTISRELAELLSGRIEAESTPGQGSRFRLVLPARQSEARAQAAAAAQATISIAEKAKAPAAAKFMESFVPDISISNPKLLQFSEMEDDRDRIEPGDAVLLIIEDDAAYAAILLKLARNRGFKALVAFQGDQGLALAHAYKPDAIVLDTDLPVLDGRSIISRLKSRPELRHIPVHVISTEDRDQQTLSLGALSFWKKPSGEDELATAFLEIDSYIRRKEKSLLIVEDNADLRHSLVAYIGHPDVRITAVGSGREALEQLMMQHFDCMVLDLGLSDISGFDLLEQVKTNRKLQTLPTIIYTGKELSRQDEQKLKQYAESIVIKNVRSMERLYDETALYLHRRTADLPPDKRQLIEKLHDPAAAFEGKRILIVDDDMRNIFALSSVLEGYNMDISFAQNGREAVRLLRETPDVELVFMDIMMPEMDGYETMRAIRSDPAFRTLAIIALTARAMEEDRIRCLDAGASDYMPKPINTTQLVTMLKTWLIN
>NZ_CP045802.1|WP_052333493.1|815235_816465_-|hybrid-sensor-histidine-kinase/response-regulator
MHRQSDIPVNILLVDDRPDEYTSIAALLQDRPYKLLGATSGMLALKALLENDIALILMDVLMPDMNGFETARRIKMRKKSQDIPIVFLTSLTSELEDYMKAYSAGAIDYITKPLHPDILLSKIDAFASFYLARKELQLKSDQLLLRTQELEARNREMTALKEQAEAALRVKSGFLDMISHEIRTPLGGILSMSELMLEGNLPEEERHHAEVIHKSGQGLMTIVNQILDYSRMENGKMELHRQPFELEVVLGDTLDLFRPMAEERGLSLESYVAPSLPRTLIGDAGRLKQVLSNLIANAIRHTEAGGVKVYVNERGASDASLQLEFVVEDTGIGIPPDKMDLLFQPFIQLDAPSAKRGGTGLGLSISKTLVELMGGTISASSQVGDGTMFIFTILAALSLDGDSAEEKAE
>NZ_CP045802.1|WP_153782778.1|828487_829228_-|MOSC-domain-containing-protein
MISTKENDERMRIGQTSEIWRYPVKSMGGERLQGVSVERYGLEGDRFCSLYDEAKEGWSSYHTARKFPALLMYRAAYGEEGVRVDSPLGPSYRWEPALGDELEQVTGTRMSMSAEGAPGREGNGLMAVDAASVLIVTDASLRRLKAAWGKEAEALRFRPNLLLRTDEPELDDESLLGARLRIGGALLQVDSFCQRCSMVNYDPDSLERDPSLLRVVNDRFGLSFGLYASVLEPGRIAEGDAALREG
>NZ_CP045802.1|WP_153782779.1|829202_830441_-|MFS-transporter
MNPIPDEPGRIVRGSDDYRRAGRSLFVAGAATFGMLYSVQPLLPEFAREFGQTPAGASLTLSVSTVLLAAALPIAGLLSDRIGRKRVMEASLLLASLICLAAALAPGFASLLALRALLGILLAGLPAVAMTYLAEEMDPASLGAAMGLYISGNSIGGLAGRGAVSTISDLAGWRWGVGAVALCGLLAAWQLMRRLPEPRRSAANRTTPQEMLAHSRRHLRRPVLLALFGIGAVLMGGFVTLYSYLAFRLLAPPFELPQAWVGWIFILFLTGSVSSPLMGRLRDRRAALGLALGLLAAGLALTLPEQLGLTLLGTALFTAGFFGGHAVASAWVGAAAPAGRAQASSLYLLFYYAGSSLGGTAGGLAWSAAGWPGVVRLIGGMLAAGLLLWLALCLLPSARLSARPYDLDKGER
>NZ_CP045802.1|WP_028600080.1|830623_831571_+|ribose-phosphate-pyrophosphokinase
MTDKVKIFSGSSNVPLAKSISEQLGLPLGEVTLSQFDNGELYVSYGEPIRTCHIFIVQSLSDPVNENFMELLIMIDAAKRASAKTINIIMPYYGYARQERKRHPREAISAKLVADLLHTAGASRIITLDLHTAAIQGFFTFPVDHLTALDELTEHIRAKNIENPVIVSPDAGRASTAEKLANYLHAPFAMVVTNHDPHTGEEKMHVIGDVKDKTPVIIEDIIDTGRTLFNVVEKLVEKGGRDVVIAATHGLFSGDALEKLNHPHIREIVVTDSILQQASPSDKLTVIPTAGLFTEAIRSNIYGGSIATLFKNRGI
>NZ_CP045802.1|WP_101809403.1|831863_833615_+|sensor-histidine-kinase
MLLLLSVLMIGCFVFYQLVLGYVFRIYDRQIYEKSSQVLGTSSIAIENRLREVEGLSFRVLADPVIQQALGKLSGSPTSYEQNVLRKRVADQLISYAGSEKDVYSILLIDTRGIPISAGNREGITAGMQLDLVALAERTDGAHAWKVTADKRAALLSVRKIRSFTTQNLTFDNLGTLIIRTRIDRIIEDQMDTGPGQARLILTDGKDIIYPLADDMPLTAAEAARTAAQGKPYGVESYAGGEYFTALMASKNMGWTYLYVTPFDEMFRQLTAVKRIVLASFVAIFLAALLLGAMLSSSINRPMLLLLRKMRQIEKGQLDRLEEQSLGAVPELSHHEAGILHRTFTMMLQRIRELIDENYAKQLTIREAELKALQAQINPHFLYNTLESINWQAKMNGQRSISEMVEALGHLMRSSISGTEDLLPLEQELELVRSYVTIQAIRYEERLDFRLEAEEEALPALLPKLTLQPLVENAVHYALEPMIEPCVITVSASTSGGRLRLAVSDTGPGMPPEFVERLRRGEVRTRGQGIGLANIAERLRLTYGGDASLEIESAEGKGTTVRLDMPYTEEREETSHAKRAAGR
>NZ_CP045802.1|WP_101808523.1|833589_835242_+|response-regulator
MRSVLLVDDERLIVEGIAKVLDWSGLGLRLAGTARNGLEALEAIERERPDLVLTDIRMPGLDGLGLVERTAERHPRIRFAMLTGYKDFDYARRAMQHGVRHYLLKPCSEQQIGEALTELARELEEEDERDGFLSEMEQRYRRMLPHVKEQFLKEFITNRTYGSRDLALYQSLFGMELDGRPVRLMLLSPAGEPDYAQLFALSNIAAELIPGILLSTTIDGTLLVVLDDGGEPDDEAARGTDGAVEAVGTMRVKEAKAGSPQRLAPELEARIGRVQETFRRFYKLEATAALSSAGRMVEARRLYREARECLAHRFYVGDDSLIVRSDLPAAQGAEALPEPDEERLCLLLRSGLADEARLEIERFLGELAERRAALPAARSCVLQLYAAMIRVCPEAEAEAFTLRAAELSGIDTLAGLGEFVTDSAMRLADHYHRLTLSRQSSAVERLIAIIEQDYADSGLTLGAVAAGQLFMNADYVGKMFKKATGESFSAYLNRHRIREACRHIRSGGDARVAELAERFGFGDNAPYFSQVFKKWTGRTPSEFKKCPSDF
>NZ_CP045802.1|WP_028600083.1|835393_836686_+|carbohydrate-ABC-transporter-substrate-binding-protein
MKRRMLGLLAAVTLASTALSACSSGNDAPAGGSADDPVSLRIAWWGSDSRHAYTQQVIDLYTSKHPNVKIDVEYASFDDYWKKLAPQAAAKQLPDIVQMDISYISQYAKNGQLAELEPYLNNQIQVGDVSESVLGTGLLGGKQYGIPIGVNVLGFHYDPELLKKGGIDSIPADWTWEKYEEMARQTGSKGLYFDSGFAPDIFFNYYLRTKGETLYNEEGNALGYDDDKLFTDFFRIQADLVKEKALRSPDYLNQIKGVLEESDLVKGTGIGVFQWSNQFVGLQKAAARPLALAPMMGPDMEKGIYMQPSMYWAITNNSKAKEEAAKFIDFWVNDVEANKIIKGERGVPISSAIKEAIAGELDEPVKQVFDFVSEMEPKASPMSPPPPTGSPEVIAALADLIEELNFGRITPEQAAASFRKTASEVLAANK
>NZ_CP045802.1|WP_028600084.1|836891_837797_+|sugar-ABC-transporter-permease
MLKRNTALRNDLTGYAFISPFVIGFLAFTLIPMFISLYLSFTSYNLFSAPRWIGLDNFVKMFTGDPKYMNSLRVTFLYVFVGVPLRLMFALFIAMLLNNGSRLIGTYRTLFYLPSIIGGSVAVSIMWRNIFGSEGIVNSALIAIGLGPVSWFGDPNAALGMLVTLSVWQFGSSMLIFLAGLKNISPEMYEAAGVDGAGPARRFFRITLPLLSPIILFNLIMQTISAFMTFVPAYIISKGEGGPMDGTMLYSLYLFRQAFMFNNMGYASAMAWVMLIIVGIMTAVLFFVSKYWVFYESEGGR
>NZ_CP045802.1|WP_028600085.1|837800_838640_+|carbohydrate-ABC-transporter-permease
MAWKTIKWPVYHLFAIALAVLMLYPVLWMLMSSFKESRLIFVTAESLLPDKWVWSNYADGWKGTAGYPFMTYIWNSLVIVVLSTIGAVLSSSLIAFGFARLSFRGRNLWFALMMVTLMLPHDVVLVPQYVIFTKLGWLNSIAPIVVPQFFGIPFFIFLMVQFIRTIPRELDEAATIDGCGKLRLYARIILPLLRSSLATAAIFSFYWRWEDLLGPVLYLNSPDKYTVSMALKMFLDSESTSNWGAMFAMSIVSLVPVIALFFAFQKHIVQGMATSGLKG
>NZ_CP045802.1|WP_153782780.1|838737_839988_+|GDSL-family-lipase
MNADLPDGDAGARQDGAAPVEGARRQAGEAPEASAAEPPATGRGAAELRFAFGPGEPPPGAAQVRADDAYSDERGWGFEPGSTVHERLRPGGEGILIPAQAVFAVAVPDGIYHVRVRCGDERHATSTSVRLGEGSLVLPLLERPAGVYAEELFAAAVRGGRLRLRLSGKAPRLCELTVTPAPQAVGLFLAGDSTVCDQPASGYPYFGWGQALPARFKHDVAVDNHAVSGRSSLSFIREGRLEAILERLKPGDWLFVQFGHNDQKNDAERFTEPFGSYKDTLRRYVSGARERQAHAVLVTSMQRRDFDAEGRLRDTHGDYPAAMRELAAEEGVPLIDLAELSRELFEAAGPEGTKDDFMWLLPGESLNHPSGTRDNTHFQERGAVRLAGLVAAEIRRLRLQPLAMYLRESAEGPGSI
>NZ_CP045802.1|WP_028600087.1|840144_840522_+|hypothetical-protein
MSQALGSRSWIIPDGYIPPLSSGSLESHESICVLNAGDEPAELELTVYFEDREPLAGIVETVPGRRTRHIRTAGLASGGERIPAGVPYAVTVASSVPVVVQYSRLDSTQPELALMSVMAHPLERS

Crispr_ID: NZ_CP045802_6

• CRISPR_ID: NZ_CP045802_6
• CRISPR_location: 921035-921538
• CRISPR_type: Orphan
• Repeat_type: I-C:NA
• Spacer_info: 7 spacers

Consensus repeat of NZ_CP045802_6

Consensus_repeat	Method
GTTTCAATCCACGCTCCCNGTACGGGGAGCGACT	CRT
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC	PILER-CR
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC	CRISPRCasFinder

spacers of NZ_CP045802_6

>6.1|921068|34|NZ_CP045802|CRT
CAAAGCCCCTTTCTGGCCCCGAGCCCTCCTGACC
>6.2|921135|36|NZ_CP045802|CRT
CTTGATGAAGTACATGCCGATCAGCGTCGAGTTCTC
>6.3|921204|33|NZ_CP045802|CRT
CGCGCCGACGATGATCCATTTCTTCTTGCCGCT
>6.4|921270|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
GCGTCTTGATCTGCACCTTGTTGTAGTAGCTGCG
>6.5|921337|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
TGGGGGATCGCGTCTAGCCCAGTAACCACCTCAG
>6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
CGCGGTCGTTCAGCGTCAGCGGCAGGTCAGCGAT
>6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
GGGGTCTGGGGCTGCGGCTCGCTGGTGCTGCTCGG

CRISPR arrays and Neighbor proteins around NZ_CP045802_6

CRISPR arrays

The CRISPR arrays of NZ_CP045802_6

>merge|NZ_CP045802|6|921035-921538|CRT,PILER-CR,CRISPRCasFinder
GTTTTAGTCCATGCTCCCCATGGGGGAGTAACTCAAAGCCCCTTTCTGGCCCCGAGCCCTCCTGACCGTTTCAACCCATGCTCCCCGTACGGGGAGTAACCTTGATGAAGTACATGCCGATCAGCGTCGAGTTCTCGTTTCAATCCACGCTCCCATGCGGGGAGCGACTCGCGCCGACGATGATCCATTTCTTCTTGCCGCTGTTTCAATCCACGCTCCCGGTACGGGGAGCGACGCGTCTTGATCTGCACCTTGTTGTAGTAGCTGCGGTTTCAATCCACGCTCCCGGTACGGGGAGCGACTGGGGGATCGCGTCTAGCCCAGTAACCACCTCAGGTTTCAATCCACGCTCCCGGTACGGGGAGCGACCGCGGTCGTTCAGCGTCAGCGGCAGGTCAGCGATGTTTCAATCCACGCTCCCGGTACGGGGAGCGACGGGGTCTGGGGCTGCGGCTCGCTGGTGCTGCTCGGGTTTCAATCCACGCTCCCGGTACGGGGAGCGAC

>NZ_CP045802|6|2|921035-921538|CRT
GTTTTAGTCCATGCTCCCCATGGGGGAGTAACT	CAAAGCCCCTTTCTGGCCCCGAGCCCTCCTGACC
GTTTCAACCCATGCTCCCCGTACGGGGAGTAAC	CTTGATGAAGTACATGCCGATCAGCGTCGAGTTCTC
GTTTCAATCCACGCTCCCATGCGGGGAGCGACT	CGCGCCGACGATGATCCATTTCTTCTTGCCGCT
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC	GCGTCTTGATCTGCACCTTGTTGTAGTAGCTGCG
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC	TGGGGGATCGCGTCTAGCCCAGTAACCACCTCAG
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC	CGCGGTCGTTCAGCGTCAGCGGCAGGTCAGCGAT
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC	GGGGTCTGGGGCTGCGGCTCGCTGGTGCTGCTCGG
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC

>NZ_CP045802|6|2|921237-921538|PILER-CR
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC	GCGTCTTGATCTGCACCTTGTTGTAGTAGCTGCG
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC	TGGGGGATCGCGTCTAGCCCAGTAACCACCTCAG
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC	CGCGGTCGTTCAGCGTCAGCGGCAGGTCAGCGAT
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC	GGGGTCTGGGGCTGCGGCTCGCTGGTGCTGCTCGG
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC

>NZ_CP045802|6|4|921237-921538|CRISPRCasFinder
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC	GCGTCTTGATCTGCACCTTGTTGTAGTAGCTGCG
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC	TGGGGGATCGCGTCTAGCCCAGTAACCACCTCAG
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC	CGCGGTCGTTCAGCGTCAGCGGCAGGTCAGCGAT
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC	GGGGTCTGGGGCTGCGGCTCGCTGGTGCTGCTCGG
GTTTCAATCCACGCTCCCGGTACGGGGAGCGAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_028600238.1|930246_930540_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153782806.1|917365_919993_+|glycoside-hydrolase-family-81	unknown	unknown	gnl|CDD|227785
NZ_CP045802.1|WP_153782805.1|916236_917088_+|hypothetical-protein	unknown	unknown	gnl|CDD|368370
NZ_CP045802.1|WP_153782812.1|927857_928424_+|histidine-phosphatase-family-protein	unknown	unknown	gnl|CDD|366010
NZ_CP045802.1|WP_028600232.1|923888_924950_-|LLM-class-flavin-dependent-oxidoreductase	unknown	unknown	gnl|CDD|274817
NZ_CP045802.1|WP_052333535.1|923227_923803_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP045802.1|WP_153782813.1|928922_929816_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028600225.1|914473_914770_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153782808.1|921908_922976_-|copper-amine-oxidase-N-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|377924
NZ_CP045802.1|WP_043111752.1|912007_912223_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153782804.1|912648_914454_+|hypothetical-protein	unknown	unknown	gnl|CDD|380149
NZ_CP045802.1|WP_153782814.1|930637_931555_+|hypothetical-protein	unknown	unknown	gnl|CDD|379220
NZ_CP045802.1|WP_153782810.1|926658_927537_+|DUF4362-domain-containing-protein	unknown	unknown	gnl|CDD|372994
NZ_CP045802.1|WP_028600222.1|910072_911014_+|hypothetical-protein	unknown	unknown	gnl|CDD|227300
NZ_CP045802.1|WP_153782807.1|920171_920777_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379112
NZ_CP045802.1|WP_028600226.1|914822_916262_+|S-layer-homology-domain-containing-protein	unknown	unknown	gnl|CDD|306825
NZ_CP045802.1|WP_153782802.1|911013_911949_+|pilus-assembly-protein-TadB	unknown	unknown	gnl|CDD|227300
NZ_CP045802.1|WP_153782809.1|924994_926485_+|hypothetical-protein	unknown	unknown	gnl|CDD|377357
NZ_CP045802.1|WP_153782811.1|927558_927861_+|Dabb-family-protein	unknown	unknown	gnl|CDD|214884
NZ_CP045802.1|WP_153782803.1|912158_912638_+|hypothetical-protein	unknown	unknown	gnl|CDD|377921

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_153782806.1|917365_919993_+|glycoside-hydrolase-family-81	gnl|CDD|227785	COG5498, ACF2, Predicted glycosyl hydrolase [Cell envelope biogenesis, outer membrane].	1.8594e-122
NZ_CP045802.1|WP_153782805.1|916236_917088_+|hypothetical-protein	gnl|CDD|368370	pfam05283, MGC-24, Multi-glycosylated core protein 24 (MGC-24), sialomucin. This family consists of several MGC-24 (or Cd164 antigen) proteins from eukaryotic organisms. MGC-24/CD164 is a sialomucin expressed in many normal and cancerous tissues. In humans, soluble and transmembrane forms of MGC-24 are produced by alternative splicing.	1.30057e-05
NZ_CP045802.1|WP_153782812.1|927857_928424_+|histidine-phosphatase-family-protein	gnl|CDD|366010	pfam00300, His_Phos_1, Histidine phosphatase superfamily (branch 1). The histidine phosphatase superfamily is so named because catalysis centers on a conserved His residue that is transiently phosphorylated during the catalytic cycle. Other conserved residues contribute to a 'phosphate pocket' and interact with the phospho group of substrate before, during and after its transfer to the His residue. Structure and sequence analyses show that different families contribute different additional residues to the 'phosphate pocket' and, more surprisingly, differ in the position, in sequence and in three dimensions, of a catalytically essential acidic residue. The superfamily may be divided into two main branches. The larger branch 1 contains a wide variety of catalytic functions, the best known being fructose 2,6-bisphosphatase (found in a bifunctional protein with 2-phosphofructokinase) and cofactor-dependent phosphoglycerate mutase. The latter is an unusual example of a mutase activity in the superfamily: the vast majority of members appear to be phosphatases. The bacterial regulatory protein phosphatase SixA is also in branch 1 and has a minimal, and possible ancestral-like structure, lacking the large domain insertions that contribute to binding of small molecules in branch 1 members.	3.23996e-25
NZ_CP045802.1|WP_028600232.1|923888_924950_-|LLM-class-flavin-dependent-oxidoreductase	gnl|CDD|274817	TIGR03858, LLM_2I7G, probable oxidoreductase, LLM family. This model describes a highly conserved, somewhat broadly distributed family withing the luciferase-like monooxygenase (LLM) superfamily. Most members are from species incapable of synthesizing coenzyme F420, bound by some members of the LLM superfamily. Members, therefore, are more likely to use FMN as a cofactor.	0
NZ_CP045802.1|WP_052333535.1|923227_923803_+|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.	9.52526e-10
NZ_CP045802.1|WP_153782814.1|930637_931555_+|hypothetical-protein	gnl|CDD|379220	pfam13491, FtsK_4TM, 4TM region of DNA translocase FtsK/SpoIIIE. 4TM_FtsK is the integral membrane domain of the FtsK DNA tranlocases. During sporulation in Bacillus subtilis, the SpoIIIE protein is believed to form a translocation pore at the leading edge of the nearly closed septum. The E. coli FtsK protein is homologous to SpoIIIE, and can free chromosomes trapped in vegetative septa.	0.00868903
NZ_CP045802.1|WP_153782808.1|921908_922976_-|copper-amine-oxidase-N-terminal-domain-containing-protein	gnl|CDD|377924	pfam07833, Cu_amine_oxidN1, Copper amine oxidase N-terminal domain. Copper amine oxidases catalyze the oxidative deamination of primary amines to the corresponding aldehydes, while reducing molecular oxygen to hydrogen peroxide. These enzymes are dimers of identical subunits, each comprising four domains. The N-terminal domain, which is absent in some amine oxidases, consists of a five-stranded antiparallel beta sheet twisted around an alpha helix. The D1 domains from the two subunits comprise the 'stalk' of the mushroom-shaped dimer, and interact with each other but do not pack tightly against each other.	5.37806e-15
NZ_CP045802.1|WP_153782811.1|927558_927861_+|Dabb-family-protein	gnl|CDD|214884	smart00886, Dabb, Stress responsive A/B Barrel Domain. The function of this domain is unknown, but it is upregulated in response to salt stress in Populus balsamifera (balsam poplar). It is also found at the C-terminus of a fructose 1,6-bisphosphate aldolase from Hydrogenophilus thermoluteolus.It is found in the pA01 plasmid, which encodes genes for molybdopterin uptake and degradation of plant alkaloid nicotine. The structure of one has been solved and the domain forms an alpha-beta barrel dimer. Although there is a clear duplication within the domain it is not obviously detectable in the sequence.	7.29173e-24
NZ_CP045802.1|WP_153782804.1|912648_914454_+|hypothetical-protein	gnl|CDD|380149	NF012181, MSCRAMM_SdrD, MSCRAMM family adhesin SdrD. Features of this protein family include a YSIRK-type signal peptide at the N-terminus and a variable-length C-terminal region of Ser-Asp (SD) repeats followed by an LPXTG motif for surface immobilization by sortase.	5.10194e-08
NZ_CP045802.1|WP_153782810.1|926658_927537_+|DUF4362-domain-containing-protein	gnl|CDD|372994	pfam14275, DUF4362, Domain of unknown function (DUF4362). This family of proteins is found in bacteria. Proteins in this family are typically between 93 and 146 amino acids in length. There is a conserved IRIV sequence motif.	2.58432e-11
NZ_CP045802.1|WP_028600222.1|910072_911014_+|hypothetical-protein	gnl|CDD|227300	COG4965, TadB, Flp pilus assembly protein TadB [Intracellular trafficking and secretion].	9.74037e-29
NZ_CP045802.1|WP_153782807.1|920171_920777_+|GNAT-family-N-acetyltransferase	gnl|CDD|379112	pfam13302, Acetyltransf_3, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.01663e-24
NZ_CP045802.1|WP_028600226.1|914822_916262_+|S-layer-homology-domain-containing-protein	gnl|CDD|306825	pfam00395, SLH, S-layer homology domain.	6.5098e-05
NZ_CP045802.1|WP_153782802.1|911013_911949_+|pilus-assembly-protein-TadB	gnl|CDD|227300	COG4965, TadB, Flp pilus assembly protein TadB [Intracellular trafficking and secretion].	7.6806e-16
NZ_CP045802.1|WP_153782809.1|924994_926485_+|hypothetical-protein	gnl|CDD|377357	pfam04439, Adenyl_transf, Streptomycin adenylyltransferase. Also known as Aminoglycoside 6- adenylyltransferase (EC:2.7.7.-), this protein confers resistance to aminoglycoside antibiotics.	1.16326e-159
NZ_CP045802.1|WP_153782803.1|912158_912638_+|hypothetical-protein	gnl|CDD|377921	pfam07811, TadE, TadE-like protein. The members of this family are similar to a region of the protein product of the bacterial tadE locus. In various bacterial species, the tad locus is closely linked to flp-like genes, which encode proteins required for the production of pili involved in adherence to surfaces. It is thought that the tad loci encode proteins that act to assemble or export an Flp pilus in various bacteria. All tad loci but TadA have putative transmembrane regions, and in fact the region in question is this family has a high proportion of hydrophobic amino acid residues.	2.37728e-07

Protein sequences

>NZ_CP045802.1|WP_153782807.1|920171_920777_+|GNAT-family-N-acetyltransferase
MGNHVSSSGEDQILRLDGEHIMLREFIAEDLDRFHSLTWQPEIHSYLPGWNVSKDTRKEWLLQYEIPETKRFLQAVKQKEDVGELRLRLGIILKETGELIGWCCSGIKDELPWPNREIMYAVSKDHRGRGYAAQAAQAMIRYLFDQADVEALCAVALVRNLPSNRVLEKCGFDFQGKLEIEQDEYNSYVLRRSNGERAMTE
>NZ_CP045802.1|WP_153782806.1|917365_919993_+|glycoside-hydrolase-family-81
MNKRIAWLLLLSLLAAVAVPAGAATAYSGEVALGAGSYSTVLPPGAVNVQSQIYKTGNVTGAMPTNDWWSNLAWDTYSEAQYPHPLAMKNGSGGIRIYYPGNRITANSSCVCGWINDIHDFTVGHSAVASFPDAKVDGFSDWFVKAQYKSGASEMNVSYGHGSPYVYFTYAGGSPKISFYDTPTIWSGSASTPVLGITVAGAHYGLFGASGTTWSGIGDKTLTNSGTSYFSVAALPDNSAATLSKFAQYAYSHVTGTTASYSYNASASEVTTTYAFTTQAKQGTQTGTLFALYPHQWKNSSTALTSYAYNSVRGQMKVGEGSSFQTKMKYYGVLPSLPDKGSYNRQQLQQYVDQAEAETYTGDGDTYWIGKRLGKLASLAPIADQVGDTTAANKFRSEIKTILQSWFKSSDSAGNLKSSQVFYYNNTWGTVIGYPASYGSNNELNDHHFHYGYFIKAAAEIARVDKAWATQWGPMVNLLIRDIASSSRSDSMFPYLRNFDPYAGHSWAAGHARFGDGNNNESSSEGMNAWAGMILWGQATGDTTARDTGIYLYTTEMNAINEYWFDVNNQNRPAGFTRSTASMVWGGKTVGDGTWWTGNPEEVHGINWLPFTGASLYLTQYPDYTTRNYNALVSENGGTSFDAWEDLIYMYRAISNPGEAKSFWTSRGGALSAEAGNSKAFAYHWIYNLDAIGNQDRTVTANTPAYAVFNKNGVKTYTAYNLTNSAITVTFSDGKTMSVPANGSATEGAGGSNPTPTPTPTPTPTATPTATPTPTATPTPTPPAGQTYTHADFTATVTKSGSSESIAFTPSTAAAYVDVHYLVNGANQQNVRMIKSGSTWTHTIQGLTSGQSIELWFTYEKSGPQYDSPHYTYTH
>NZ_CP045802.1|WP_153782805.1|916236_917088_+|hypothetical-protein
MPKSRRRTEMDALDGARRGRLARLLRDERGGMSLLGIGMMAMFILLAIYLFYFYTVFIEKRQAQNVADAAALAAVETIKELYEEALEQEAGAQARKLHEGEQEARRTPEPTPTSVPTPTPSSPAGGLPDATATPTSTPTPSAPPSERGEFDDERLYDEIVEEERFRDADWLSDNWMRIVRERYFADSFTATRNGDLLYDTVKRHSGRISAAARETARRNEGLPNGGLEFPYERKPKFLLESGRTITLETIGIRSDLTAKAAAALGSKEIPIDVSSKVPMMIYW
>NZ_CP045802.1|WP_028600226.1|914822_916262_+|S-layer-homology-domain-containing-protein
MKPSSTSKAAALLLLTGMVAAACSGGNAEQPSPKPSAAASPSATEGPVGTPVPTASAAPASVVVTDIGDHKFREQIVKLLESGIATPSSGGLFEPSAPVTKGDFLRWMTAYDDKGLEDADLSKPPMYPDLEADSPDYGWIHGLVEAGRLGAEPGKPLQLDGPLQRGELARLWAWYQDRASIKESDRDRLSSEVVIMSREDRKEIPEPYIRAVAHYVSVADGKPYLRTFGDTSRLAAEALVSRSQAAYWIVENAGEESGGDGFSPPAPKVQVEVQGIEEAAPAAAPSDIAGHKREAAVAKLAGQVAGVLDGSGAFRPDEPILRFEFIRWMAAYDDKGVIPFRAPEPTYSDVKQQDEGYELVEGLTQAGIISGFPDGTMRLSEPLTREQLTVLWGWYQRYGLVVKPLAAEVSEVNLRNFEDRDKVGKIFLGGVQAYVSSNWDTPPYLDTFGADKKLEPQKPVTRAEAAYWITQNAEVEAED
>NZ_CP045802.1|WP_028600225.1|914473_914770_+|hypothetical-protein
MIEKIRRMDEKKLTKAMTAANIFFIAGCFLIAYLGGNHDYITFETGIWLFLLFFLPALAVMILMYIRGDAQTRRSYLIRIVLAVVVFGGLNLYRFYMN
>NZ_CP045802.1|WP_153782804.1|912648_914454_+|hypothetical-protein
MRPIRIRSWTRALILLMLLLGGAAHAAVPALAEADSGIGTGLDSYEIPDKGAEKPASSIEVAVPDGSTGRPDYDAGDAASPGPPDPGSTGDSDDTDPGSADPGEVDPGSADPGQTDPGGADPGVTDPGGADPDGADPDGTTDPGRVDGGNTDTDGTTDRDGTTDTDGTTDPDGTTDPDGTTDPGSTDGGDTEPGDTDSGDTDSGDTDPGDIDPGTSDPGKSDPGGADTDGGKPWYEKLWDNTVQFAKGAGGGLLGAAIVVGVVVGVAAIIGITFAAPVIIAALVVGAIAGGIYALVAGDSFSFVKAMGIGGLAAGTVLTLGHAGVFGAVRGGIQLVRSAGLKSALRTAGSRMASFAKSAMGNLKSGFLNMAKHPVAALKSTLTSKTFQFSTAVNMVMNMGIKMTFEGKLPTVGEVGLMAVESFVGALVFDRVGDALGAAARSPLGKRVAATFSQTFENVIVALAKPKEKLDPETAAASGFFKGFVLQSLFGGRLNRLRSEQDIGTSFSDLGGRTVETVVPNRNRTITNIELNRIWNDTANANNISRWDDSGNRVTQRQLDQLQRNQDALDRLQSREGSLQEAVEVGGDEAIKQGKPLLDKN
>NZ_CP045802.1|WP_153782803.1|912158_912638_+|hypothetical-protein
MVALLRSSRRKSKASSTRSRFKSASGGRQAVRPLFRSLRDERGAQAIEFVGIVPLFLLMVLVVVQFALVGMTAVVAKQAAMEGARAAMVADGAGPHYEQAVRNTAGSYGIREISRSESGEYVTVRVVLESPMVTGSLFGSGWAVPISTQVTVMKEKANE
>NZ_CP045802.1|WP_043111752.1|912007_912223_+|hypothetical-protein
MIRTLGIHLYAKAQQARSYLSNQRGAQAIEYIGIAAVAVVLIIALLSMFGDGGIASKLKEKIEGFIDKIKI
>NZ_CP045802.1|WP_153782802.1|911013_911949_+|pilus-assembly-protein-TadB
MQMEWPVRLLYAALGLWALSMALFGWFWIKRISLMQRLGLIEKEKKKKDRLPARIAALVFRWSEGLTPLGRRFKLFASDELLERRLALAGHPHGLTLDTFYGFRFLCLFAGLLAGTMLSLIGFSSIFVLLLFGLGLVWPSLWLRSAAAGRQDQIGVDLPDFMDAMSVTLQAGVPLDPAMKQIVRTMEGPLREELGRFQQELDIGVPREQAYMRLMNRNQSKPLEMLILSLLQGSRLGVPISSTFKTLAEDMRDVRVSAVKERAAKAGPKVTLITTFVILPGVILFIVGMLVLNFIYNPEGIGFSWDGLNGL
>NZ_CP045802.1|WP_028600222.1|910072_911014_+|hypothetical-protein
MPEHSLFLLTVFAAAALGLYGMIELVQARRGMNALSRKLTPLHTEEARASRSAVRRLSLRLDASDYGRGWADRLQAAHIKLTPLQWLSLLSGAWAVISLLIASLLSLGFPYNLLIAYLAVNLGSKQILKSRRQKFGEQINRQLPEICRMLSSCVRAGMSIQQGIDMVAREIKPPAGFLFQTMSRELQMGTGVGDVLERVHERFTSKDIRLMTQTILVQRQAGGNLGAALDHLARTLEERERVNREISNQTAESRYIAVTLALMPVFLVFVFNMVFKGFITPIFTLPGLILLAAVVVLMAIGFVLIQKVSRIKA
>NZ_CP045802.1|WP_153782808.1|921908_922976_-|copper-amine-oxidase-N-terminal-domain-containing-protein
MKKPTKTIPALLSVAALSLAASSVIAASPAGAIVPISAPLPDSSVQNEQQQPAVPNYMSVTGTVKEISDSKTKEGAKTVSLQDDKGEIIANVTVSGDTYVAAPDKLQAGTKWNAYYDAKKPMLMIYPPQFEAEVLVPVEETASWKVDRFKAAEGDAGQLISEDGQLVLNVSEQTPLVLEDGTAFTGDLKGRALAVKYSVTTRSLPPQTSPEQIVVLFEEAVPPIGTLPEPGEGGTIDVAGFPIVVEGKKLAGPSPYTSKDGTVMVPLRAVVEALGQKLTWDASTKSSRIGLATTLTVGKDYYVYNKMAPIELGAAPALVDGKTYVPLQFFRDVMMLNNAYVFEGQIDINNQEKME
>NZ_CP045802.1|WP_052333535.1|923227_923803_+|GNAT-family-N-acetyltransferase
MTGLSKRPPKLIPACWSTERLTVREVSPEDETAASRLFVEAGPLPEWTGRSAEEGYVGRVLKGNPDVPPGGSADRVRLQLAWLREEDGAARPAAILELYHGYPGEEDLYIGYFGVDASLRGTGIGRELVEGIAAQAEALGFRRIRAAVDLKNWTGLRFWVTLGFAEAVKVVGDAVLSASTFGQIELARRLG
>NZ_CP045802.1|WP_028600232.1|923888_924950_-|LLM-class-flavin-dependent-oxidoreductase
MNDMASMEIGISTFLEAAPHPGTGQPKNHAERLREAVEEIVLADQVGLDVYGIGEHHRPDYAGSAPAVILAAAAAQTKHIRLTSAVTVLSSDDPVRVYQQFATLDGISNGRAEIMAGRGSFIESFPLFGYSLDDYNELFDEKLELLLDIAKSEKVSWRGGLRPAIEDRGVYPRAVQDPLPVWIATGGNSQSTIRAGLLGLPVAYAIIGGMPESFAPLVDLYKRAAAQAGHDVSKLQIATHSHGFLADTKQAAADLLYEPYRAQMNKIGAERGWQASFDRRAFDAACDPRGALYVGDPEYVAEKILLLHKNLGVTRFFHHVDVSAVPHRDVLRSIELLGTKVAPIVRRELAKLG
>NZ_CP045802.1|WP_153782809.1|924994_926485_+|hypothetical-protein
MFLNYSKSKGGAGMRKTDVRPWTPQWRERAETEMAWLEAMLGGELLELHHIGSTSVEAIGWAKPVVDLLAVVRSVQALDALEDAFAQLGYEAKGENGIPGRRFYAQGGDRRTAHLHAFEAGAPQIGVHLRFRDYLEAHPERARAYGEHKRELAERFPDDTHAYQEAKQPFVQRLVQEAEAWAEAAERMAAGDAEARKLESESGEDSARPPRRSEDEMTALILGVARADERVRAVCLNGSRVNPLAPRDKLQDYDVVYLVTELDAYLTDDSWIDVFGERVILQMPERMGLIPPDGGGRFAYLMQLADGNRIDLRLIPLEQTDAYLAEDRLTRILLDKDGRLPELPEPSDADFHVRPPRGSEFADCANEFWWVSTYVAKGLWRDEPLYALDHLNGPVRAMLLQMLDWQAGARHGFAVSTGKSGKYLDRWLPAESWQALLATYPSADRESVWTALLRMAELFRSSARDVAARLGLAYDEEEERRVRRYLLEVKSDTGQR
>NZ_CP045802.1|WP_153782810.1|926658_927537_+|DUF4362-domain-containing-protein
MKRMLHPKALAALLLAGLLAGGCSSGPELPSGSGAQASSGSPAPAEAQAEAGALPEQGRAAVVSRSLGFGEVNPAPLALFEESAEIEPFEEAIRSSERIEGILDVAEPDLDLVLQSESGARKAYHLWLPLGGPRTEGMKGMAMEVANTHTGYTISAAAAKQLAELVLSKGYTSEQAVKNGDVVFGLRGQFNADVWQAFAEKVGRGEEAAVQITSYTIEGAPIFENLSLEDGTIRYRRDDRFDGYATKEHPRIYFCKRLEEGEAGEDTVYSLAECGEEASPFLLRLSGTGGGS
>NZ_CP045802.1|WP_153782811.1|927558_927861_+|Dabb-family-protein
MMEHLVSFKFNRPLEAAEQEELLALLRGLRGQVPGIIELTCGFNETEETDNIHGFTLGLRVTFTDREALRDYGPHPAHQAFVSRLEGLVEQVVVVDYPFG
>NZ_CP045802.1|WP_153782812.1|927857_928424_+|histidine-phosphatase-family-protein
MSPAADKTIYLIRHARASGQEPQAELTAEGAVQAERLAELLAGRGIERIVSSPYLRALDTIAPFAAAAGLPVEEDARLAERVLSAAPLPDWEERLRASFLDPELRLDGGESGREALERGQAAIAELERSVGAGKAAAAVSHGNLLALLVGAFDPAFGYDGWRAMRNPDVFELAIGEGGARIRPIRDGK
>NZ_CP045802.1|WP_153782813.1|928922_929816_+|hypothetical-protein
MTISPWLWPLPVLAVLALAFIYSRRKEQERHLLWKLLGYLLLGAFMLRLNGFPLPLGYALFLLLLQAKPKPNRAAKHSAAFAGLLLFFLALALPAAEQSWLERERSYPVEAAQISQLSLQDDWERFKGEDAASSEDRLERFEFVYDRSGAVIQLNYAVSVWSGNGSYRYQVEYAPEKGHAVVQRLGRDGGGSPPDGLSAELVLERLRPEVLAELAPAPERADADRLRLEVPTMWFANGTAFLDPKGFQPAFRIGHDGEVEPLPNVAEPYETAAAVVVYGCRDPELFEGCAAPAYYLF
>NZ_CP045802.1|WP_028600238.1|930246_930540_+|hypothetical-protein
MLGSVLMLFWLLVAIVILASLYAQREREEEWLFLKLIGCYLLGGFVLFLSVLPVPLGFILYWLLLHGKMRSNRAVKESAAFWGLGVLLIRLVVGLIF
>NZ_CP045802.1|WP_153782814.1|930637_931555_+|hypothetical-protein
MVPAWVEWVPTLLAAAGLVWLYRKSSPDEPHRGWKLIGYAALGAFSFRFPAFSFPLGFLICLMLLARAKPNVRAKRGAAIAGLAIFAAGIAIPALDQRLFERERSFAVQSGQAERLDLAGDWRRIAGGGESTDERLDRFQLVQEPDGRIRSLQYQVTARDSKGDYTIEVRYEPESGQAIVERTRRRSLNDEAALSFASGSSGVYRIDPERFLQLLSPDNLERMTMEAASGPAKLRELELLLFNGPAGPVEPSPIRRLLQADGIKPAGEEPVHGYILQARGKTDSEQGKEDKFVWHVIPTQDVQPG

Crispr_ID: NZ_CP045802_7

• CRISPR_ID: NZ_CP045802_7
• CRISPR_location: 1089527-1089623
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_7

Consensus_repeat	Method
CAGTTGCCGCTCGGGCTGCCAAGGC	CRISPRCasFinder

spacers of NZ_CP045802_7

>7.1|1089552|47|NZ_CP045802|CRISPRCasFinder
GTCGGCAGCCGTCGCTTCGCCAGGGAGCCGCCGGCCGCCAGCTGCGC

CRISPR arrays and Neighbor proteins around NZ_CP045802_7

CRISPR arrays

The CRISPR arrays of NZ_CP045802_7

>merge|NZ_CP045802|7|1089527-1089623|CRISPRCasFinder
CAGTTGCCGCTCGGGCTGCCAAGGCGTCGGCAGCCGTCGCTTCGCCAGGGAGCCGCCGGCCGCCAGCTGCGCCAGTTGCCGCTCGGGCTCCCAAGGC

>NZ_CP045802|7|5|1089527-1089623|CRISPRCasFinder
CAGTTGCCGCTCGGGCTGCCAAGGC	GTCGGCAGCCGTCGCTTCGCCAGGGAGCCGCCGGCCGCCAGCTGCGC
CAGTTGCCGCTCGGGCTCCCAAGGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_153782881.1|1086983_1089476_-|hypothetical-protein	unknown	unknown	gnl|CDD|223107
NZ_CP045802.1|WP_153782882.1|1089662_1091477_-|hypothetical-protein	unknown	unknown	gnl|CDD|366353
NZ_CP045802.1|WP_153782884.1|1096001_1096721_-|glycosyl-hydrolase	unknown	unknown	gnl|CDD|235746
NZ_CP045802.1|WP_101808590.1|1093095_1093899_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|224097
NZ_CP045802.1|WP_153784659.1|1099941_1100853_+|glycine/betaine-ABC-transporter	unknown	unknown	gnl|CDD|270357
NZ_CP045802.1|WP_153782879.1|1083094_1084570_+|DHA2-family-efflux-MFS-transporter-permease-subunit	unknown	unknown	gnl|CDD|129794
NZ_CP045802.1|WP_043111083.1|1084721_1085156_-|hypothetical-protein	unknown	unknown	gnl|CDD|226720
NZ_CP045802.1|WP_101808589.1|1091917_1093096_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|226361
NZ_CP045802.1|WP_153784657.1|1080958_1081987_+|ribokinase	unknown	unknown	gnl|CDD|238579
NZ_CP045802.1|WP_153782883.1|1093895_1094744_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|224098
NZ_CP045802.1|WP_028598076.1|1099077_1099923_+|proline/glycine-betaine-ABC-transporter-permease	unknown	unknown	gnl|CDD|226644
NZ_CP045802.1|WP_153784658.1|1085204_1086176_-|aldo/keto-reductase	unknown	unknown	gnl|CDD|381313
NZ_CP045802.1|WP_153782877.1|1079072_1080821_-|M3-family-oligoendopeptidase	unknown	unknown	gnl|CDD|341069
NZ_CP045802.1|WP_101808594.1|1097882_1099103_+|glycine-betaine/L-proline-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|226643
NZ_CP045802.1|WP_153782876.1|1078553_1078955_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153782880.1|1086277_1086916_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028598078.1|1097058_1097634_-|transcriptional-regulator	unknown	unknown	gnl|CDD|224427
NZ_CP045802.1|WP_028598088.1|1077916_1078411_-|cation:proton-antiporter-regulatory-subunit	unknown	unknown	gnl|CDD|223564
NZ_CP045802.1|WP_153782878.1|1082229_1082853_-|TetR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP045802.1|WP_101808592.1|1094740_1095817_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270381

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_153782881.1|1086983_1089476_-|hypothetical-protein	gnl|CDD|223107	COG0028, IlvB, Thiamine pyrophosphate-requiring enzymes [acetolactate synthase, pyruvate dehydrogenase (cytochrome), glyoxylate carboligase, phosphonopyruvate decarboxylase] [Amino acid transport and metabolism / Coenzyme metabolism].	9.61246e-21
NZ_CP045802.1|WP_153782882.1|1089662_1091477_-|hypothetical-protein	gnl|CDD|366353	pfam00877, NLPC_P60, NlpC/P60 family. The function of this domain is unknown. It is found in several lipoproteins.	3.08678e-23
NZ_CP045802.1|WP_153782884.1|1096001_1096721_-|glycosyl-hydrolase	gnl|CDD|235746	PRK06215, PRK06215, hypothetical protein; Provisional.	1.15365e-94
NZ_CP045802.1|WP_101808590.1|1093095_1093899_+|ABC-transporter-permease	gnl|CDD|224097	COG1176, PotB, ABC-type spermidine/putrescine transport system, permease component I [Amino acid transport and metabolism].	2.05399e-76
NZ_CP045802.1|WP_153784659.1|1099941_1100853_+|glycine/betaine-ABC-transporter	gnl|CDD|270357	cd13639, PBP2_OpuAC_like, Substrate binding domain of Lactococcus lactis ABC-type transporter OpuA and related proteins; the type 2 periplasmic binding protein fold. This subfamily is part of a high affinity multicomponent binding-protein-dependent transport system specific to betaine compounds for osmoregulation. The periplasmic substrate-binding domain, which is often fused to the permease component of the ATP-binding cassette transporter complex, is involved in uptake of osmoprotectants (also termed compatible solutes) such as glycine betaine and proline betaine. Many microorganisms accumulate these compatible solutes in response to high osmolarity to offset the loss of cell water. This domain belongs to the type 2 periplasmic binding fold protein superfamily (PBP2). The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.28955e-69
NZ_CP045802.1|WP_153782879.1|1083094_1084570_+|DHA2-family-efflux-MFS-transporter-permease-subunit	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	1.57708e-104
NZ_CP045802.1|WP_043111083.1|1084721_1085156_-|hypothetical-protein	gnl|CDD|226720	COG4270, COG4270, Predicted membrane protein [Function unknown].	1.08294e-09
NZ_CP045802.1|WP_101808589.1|1091917_1093096_+|ABC-transporter-ATP-binding-protein	gnl|CDD|226361	COG3842, PotA, ABC-type spermidine/putrescine transport systems, ATPase components [Amino acid transport and metabolism].	3.48034e-163
NZ_CP045802.1|WP_153784657.1|1080958_1081987_+|ribokinase	gnl|CDD|238579	cd01174, ribokinase, Ribokinase catalyses the phosphorylation of ribose to ribose-5-phosphate using ATP. This reaction is the first step in the ribose metabolism. It traps ribose within the cell after uptake and also prepares the sugar for use in the synthesis of nucleotides and histidine, and for entry into the pentose phosphate pathway. Ribokinase is dimeric in solution.	8.23192e-110
NZ_CP045802.1|WP_153782883.1|1093895_1094744_+|ABC-transporter-permease-subunit	gnl|CDD|224098	COG1177, PotC, ABC-type spermidine/putrescine transport system, permease component II [Amino acid transport and metabolism].	1.89058e-82
NZ_CP045802.1|WP_028598076.1|1099077_1099923_+|proline/glycine-betaine-ABC-transporter-permease	gnl|CDD|226644	COG4176, ProW, ABC-type proline/glycine betaine transport system, permease component [Amino acid transport and metabolism].	1.69585e-135
NZ_CP045802.1|WP_153784658.1|1085204_1086176_-|aldo/keto-reductase	gnl|CDD|381313	cd19087, AKR_AKR12A1_B1_C1, AKR12A, AKR12B, AKR12C families of aldo-keto reductase (AKR). Streptomyces fradiae TylCII, Saccharopolyspora erythraea EryBII, and Streptomyces avermitilis aveBVIII are founding members of aldo-keto reductase family 12 member A1 (AKR12A1), B1 (AKR12B1), and C1(AKR12C1), respectively. TylCII acts as a NDP-hexose 2,3-enoyl reductase. EryBII is a mycarose/desosamine reductase involved in L-mycarose and D-desosamine production. aveBVIII functions as a dTDP-4-keto-6-deoxy-L-hexose-2,3-reductase.	2.60121e-133
NZ_CP045802.1|WP_153782877.1|1079072_1080821_-|M3-family-oligoendopeptidase	gnl|CDD|341069	cd09606, M3B_PepF, Peptidase family M3B, oligopeptidase F (PepF). Peptidase family M3 oligopeptidase F (oligendopeptidase) is mostly bacterial and includes oligoendopeptidase F from Geobacillus stearothermophilus. This enzyme hydrolyzes peptides containing between 7 and 17 amino acids and may cleave proteins at Leu-Gly. The PepF gene is duplicated in Lactococcus lactis on the plasmid that bears it, while a shortened second copy is found in Bacillus subtilis. Most bacterial PepFs are cytoplasmic endopeptidases; however, the Bacillus amyloliquefaciens PepF oligopeptidase is a secreted protein and may facilitate the process of sporulation. Specifically, the yjbG gene encoding the homolog of the PepF1 and PepF2 oligoendopeptidases of Lactococcus lactis has been identified in Bacillus subtilis as an inhibitor of sporulation initiation when over-expressed from a multicopy plasmid.	0
NZ_CP045802.1|WP_101808594.1|1097882_1099103_+|glycine-betaine/L-proline-ABC-transporter-ATP-binding-protein	gnl|CDD|226643	COG4175, ProV, ABC-type proline/glycine betaine transport system, ATPase component [Amino acid transport and metabolism].	0
NZ_CP045802.1|WP_028598078.1|1097058_1097634_-|transcriptional-regulator	gnl|CDD|224427	COG1510, COG1510, Predicted transcriptional regulators [Transcription].	1.34124e-37
NZ_CP045802.1|WP_028598088.1|1077916_1078411_-|cation:proton-antiporter-regulatory-subunit	gnl|CDD|223564	COG0490, COG0490, Putative regulatory, ligand-binding protein related to C-terminal domains of K+ channels [Inorganic ion transport and metabolism].	1.84591e-42
NZ_CP045802.1|WP_153782878.1|1082229_1082853_-|TetR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	3.15648e-12
NZ_CP045802.1|WP_101808592.1|1094740_1095817_+|ABC-transporter-substrate-binding-protein	gnl|CDD|270381	cd13663, PBP2_PotD_PotF_like_2, The periplasmic substrate-binding component of an uncharacterized active transport system closely related to spermidine and putrescine transporters; contains the type 2 periplasmic binding fold. This group represents the periplasmic substrate-binding domain that serves as a primary polyamine receptor of an uncharacterized ABC-type transport system from gram-negative bacteria. Polyamine transport plays an essential role in the regulation of intracellular polyamine levels which are known to be elevated in rapidly proliferating cells and tumors. Natural polyamines are putrescine, spermindine, and spermine. They are polycations that play multiple roles in cell growth, survival and proliferation, as well as plant stress and disease resistance. They can interact with negatively charged molecules, such as nucleic acids, to modulate their functions. Members of this family belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.04049e-147

Protein sequences

>NZ_CP045802.1|WP_153782881.1|1086983_1089476_-|hypothetical-protein
MIDERDAAERGSGSARFFIFPCFVGMQSMACPDSTVAPNPRHIYALVRPVSTVAPNPRHIYALVRPVSTVAPNPRHIYALVRPDSTVAPNPRHISALVRPAPGRRAGSKAHFCLGSPASRPEGRIQGTFLPWLARFPVVGPDPRHISALVGPASRPEGRIQGIFLPWFARLRPGSRAQSPLQVRFFRAPPACCPFPTAAAVHMVRDRAEGVEDRHMNGSDVVMTIWAEKGLRQIYCDRASDSSFVRELAGAARRAGLSVHGCSSLAAALSAAEGYALASGSPAAAIGTSAELSRAEAASIRALSAASVPLLLLLPGCAGRPSRSGSGFKSSALLRQEDDCRSTLEKAYFLAARHGRKGPALVRLAPSFAGERSRRPPFSMPAYEDSEDYMERLVSEPPIRDEQLDRIADGLARARRPLIVVGGGVLHAGAAAELGEFIALTDIPAAATPGGWSALAGGGRPVQNLVLPVTSLPGGRNVLPGEVPNAQTGLPAAAAPDEGSALPGGVPTARELPAQGRQAPADYVLVLGSGEPAPAASGARIDIDPAALARPEEAALERLQSDIRLFLTALSARWLARGLRRQPALLPQTPEPAPGCEAPCGPIPPAAPVPPAAELLPPGGPILPAAALPPAAPLPPASALPSASARPPAALVPSAAELLPPSGPILPAAALPPAAPLPPAAALPPASAHPPAPPVPPAAELLPPGGPLAPALASSPVDPVIPDDAADGAESCRLPGSVLLARRGWSGLPELQRLLLLEPGQRLLLLAGPAGHEADAALGASHGAPSADVTLLLPCAAGRGAPLLRPPARGAPSARVARLRRPSARPMPKA
>NZ_CP045802.1|WP_153782880.1|1086277_1086916_+|hypothetical-protein
MYSRLKKKLQELLRGKAPGGLLACRLAALPAVLAVAAAGALAAPGTAQAAPFRLDQDVVPEQSQASASELVRHADGIAVGSFGESDRMVQTGQSAPQGRLVNFVQKFTVKRWIKGGGSNELTVVTTGIEPLPPPSQLEANERYPGAWATGPDYLLFLHKLEGTDSYVPLGLLQGVYPIQGGRTVSLEDKGFPQLNGIAEAGVQQAVDRLAGS
>NZ_CP045802.1|WP_153784658.1|1085204_1086176_-|aldo/keto-reductase
MTYRKLGASGLTVSALGLGTNAFGKRTGEEESIRIVHAALDAGITFLDTANIYAGTLSETIIGKALAGRRADAVLTTKAGLPRGEGPGKRGASRAHLTAELEGSLRRLGTDYVDLYQIHTFDPETPLEETLRTLEDMVRSGKVRYIGASNYQAWELMKALGISDRLQLERYVSIQTSYSLADRTPELELVPLCLDQGIGLIPYFPLAGGILTGKYAAGAEAPPGSRLDKDGSFGRFLKGDVIGLGQDVAELAEEAGCEPAALSIRWLMDKPAVSTVIAGATSVEQLTANLRSLELALEPSIQDELERISRPFRYGEPFARYRI
>NZ_CP045802.1|WP_043111083.1|1084721_1085156_-|hypothetical-protein
MRYFQTTWPRLIGLLLFAALMVAACLYHFREPDGFAAMLPDWVPLRLPIVYATAILELAIAALVLVPATRGWTGLFAALYLVVIVVANVYAAARGIPAPGSDSASKTALWLRVAAQPLLVWWALWCTRYPSRDTSLKGPPRKAR
>NZ_CP045802.1|WP_153782879.1|1083094_1084570_+|DHA2-family-efflux-MFS-transporter-permease-subunit
MSQVAGGGPAGPELSMRAILAPLVAIIIGMFMVILDGTAMNVAVPKLQQDFGGASLSLIQWTITGYALAQAAVIPLAGWLSDRFGAKTIFILSVVLFTLGSALCAMAGSAEQLIAFRVLQGLGGGMVAPIAMAFTYRIAPPGKVGAVMGMIGIPMLLAPALGPVVSGWLVEYVSWHWIFLINLPIGVIAVIVALRTLPVIDRQTVPVLDMMGIVFGPLAFAALAYGVSEGGTDWTSARTLTGLIVGGVALVVFIIAELRRSNPLLELRVFRSPNFTKGILVQWISQAALFGTIFLLPLFLQTAKGYGALDTGLILLPQALAAGLFMPIGGRLYDKVGARPLVMTGMALVSVAAFLLSGIEADTGVGSLILPLALIGAGMGLSMMPLNTHIIQSAPAQLVGRVTSLTAAAQQVVSSFAIAGLSTYLTGRIKDNGPELGAQPAELLSASYGDTFALLIWIAATGVVLGFLLSRPKPQEGAAPSSEPGMMMGGH
>NZ_CP045802.1|WP_153782878.1|1082229_1082853_-|TetR-family-transcriptional-regulator
MPIPDKRKGSRELSASILDTARSLFAEHGVDAVSMHQIAKAAGVGQGTLYRRYAQKGDLCLCLMEEEFHRLRESILVRLEALAGEPPCVRLAALATLVVEHLIADSRIVEAMHTAIYNGRNTFKEIEQFYESPPYRFLYETIQALLDEARIKGQTIEAVDPAVSAHLLISLFSPQSLLHLHEKLEVDPEEIVRRIVCTAIRPLFRAE
>NZ_CP045802.1|WP_153784657.1|1080958_1081987_+|ribokinase
MKQGANERNGAAPEAAPQRRDVPGRAAAPPRVAVAGSLNMDLVISMGRMPLAGETISGSALHTLPGGKGANQAAGCARLGAATEMIGRVGEDAFGKQLLEQMRRMGVGASGIGVHPSEPTGVASIYHTPEDNCIVIVAGANGECGEAWVESRRESIERAQALLVQLEIPLEGVRAALRIAREAGVATVLNPAPAQQLPRELLELADYITPNETEFAALTGASAESEDELREAIAAWQASVGGRVIVTRGAAGCSFVGEDGRLVTVPAPRVEVVDTTGAGDTLNAALCVKLAELAAQGAAAGDAELLEALRFAVQAASLAVTRFGAQDGLPSREEVEAALQQA
>NZ_CP045802.1|WP_153782877.1|1079072_1080821_-|M3-family-oligoendopeptidase
MEIVSCRTTTITKEVSLVLKFSEYRYERPDREAAADAFKEKIAAMRAAASLEELLEAISAVNKLRNEIETMFQLVYIRHSINTEDAFYKAEQDYSDETSPILQEYVTDYYRALTESPFRSGIEEKYGTQLLRTAELALKTFKPEIIEDLQLENKLRTEYSQLIASARIPFDGEERTLSQLTPYTQSTDRATRKSASEAAFGFLAGNEAELDRIYDELVQVRTRIARQLGYENYVQLGYDRLGRTDYDAAMVANFRRQVREHIVPVASRLYERQQARIGVDKLHYYDEGFRFKSGNPTPKGDPDWILEQGRRMYREMSPELDEFFTFMSERELLDLLSKKGKEGGGYCTYIFDYESPFIFANFNGTSGDIDVLTHEAGHAFQVYMSRGFDVPEYLWPTMEAAEIHSMSMEFLAWPWMELFFQEDTDKYRFDHLASALSFIPYGVSVDEFQHFVYEHPEATPAERKAKWREIERVYTPHRSFDGNAYLEGGGRWQRQSHIYQTPFYYIDYTLAQLCAFQFWKRSREDFDAAWQDYLALCRLGGSKSFTALAASAGLLSPFEDGSVTSVIGEIRSWLDSVDDSSF
>NZ_CP045802.1|WP_153782876.1|1078553_1078955_-|hypothetical-protein
MMNRSGSPARWLTLLLVALILICSTPTPPILLPEAAAAGAAAESAMSRSFDTGVPVTARSYAAEREQSGPLHRPDPPSQAPSALAPPLAAAILMLAAVFAAPAWSRKLRTAPSVARRLVRCLLAPVRSASYAA
>NZ_CP045802.1|WP_028598088.1|1077916_1078411_-|cation:proton-antiporter-regulatory-subunit
MDIRETYLPGIGKKFQIKSRGGDVLIVVVHDDGRRECYMEADRDNDFKPVFSLDDDEARMLASIVGGMQYKPRALENIEMVLDDLIIEWYRVEPTYKSVGSSIGQLGVRNRSGASVLAVVEKGGATKHINPGPDLVLTEEALLIVAGERSQQKAFRDILKNGCE
>NZ_CP045802.1|WP_153782882.1|1089662_1091477_-|hypothetical-protein
MRRLIQTGTAFALIAAAGAGAAAPAGASLPSPSGSPYADAASARVLAGMAGAGAPSSLSAEADAPFSERGTPQALGGAIADYALDYVGTPYQYGGASPAGFDASGFLQYIYRFSAAEVQLPRTVAAQFENGAPVGGQSLLLPGDAVFFRSGAAVSFAGIYIGNKEFVSATVDGVKRSSLASAYWQERYAGARRMTEKAPSAGGGSGTSAGSGVGTGTGAGSGSGAGTGSGTGTGSGAGTGSGTGAGSGSSNGLAGPDQTRAAMRENAYFASVSRFLDKAKPVLDASAYNRLADKAELAFQQYEQGLYPAMLAAHEEIIDEVEALPADARSRIGIKGSELYGSSIPAGLYTVAANGELKLKNESGYSVTLSQRAAAEQLWKQVQAAYPKAYLALVKELRLDVHRGGLSRVETLAKGSVRLVLDPSDLTPGAVQKTRWSLARELGKLVTQQGPAGSQLDHLGGASSALGGAGGLVGGAFAGPAAGSSQWLYARKDSLLTAYYGKFWPAEVASAARAGKPMTTLYTKLFFRDASAYQAQEDIADAWAAFLLYDKPAKPADRRDEKILFFYAKPELVSVRAQYRSGVGLSKSYPKTTTFADLIGPRTW
>NZ_CP045802.1|WP_101808589.1|1091917_1093096_+|ABC-transporter-ATP-binding-protein
MEQVPVISFRGVTKQYEDGVPVLNDVSFDIERGKFYTLLGPSGCGKTTILRLIAGFMEPTSGEIRMDGKLINDLPANKRQVNTVFQDYALFPHLNVFDNVAFGLRIRKLKKDEIERKVEEALRFVNLEGYGKREIREMSGGQRQRVAIARAIVNEPKLLLLDEPLSALDLKLRTEMQYELRELQRRLGITFIFVTHDQEEALAMSDEIFVLNKGIIEQSGTPTDIYDEPINRFVADFIGESNIVPGRMLDDYRVEFAGKEFECVDRGLRRGEPVEIVIRPEDLEMTAAGAGKLAATVDTQLFRGVHYEIICMDDSGNEWMVHSTRKAVVGEAIGLDFDPEAIHVMRFGESEEDFDRRLEGYEEAENAEEAALRRELGEGPPIVETGRPGGNS
>NZ_CP045802.1|WP_101808590.1|1093095_1093899_+|ABC-transporter-permease
MSVRSRNLFLVPYTLWIVLFVAAPIALIAYRSLFDVEGALTLDNYARFFTPVYLRMTLSSFWYALLITLFSLLVAYPAAWALTRAKHKQLWLLLIILPTWINLLLKVYAFLGIFGTYGSVNQLLELVGIGTQQILFTDFSFVFVSVYIFIPFMILPIFNALEELNPSLVFAARDLGASAWTTFAKVVFPLTIDGVKAGCQAVFIPALSLFMITRLVAGNRVITLGTAIEQHFLVTQDWGMGSTIAVFLILVMVAIMFAAGQRKGVIR
>NZ_CP045802.1|WP_153782883.1|1093895_1094744_+|ABC-transporter-permease-subunit
MSESRRWRWSNLYLIAVFAIMYAPIFYLMAYSFNSGGTMHGYDGFTLDWYREVFADTRLLIIVLNTLVIALLSGLLSTVLGVFGALAIHEARRRRTKNTLLSFNNVLIVSPDVIIGASFLILFTMIGIRLGFVSVLLAHIAFSVPIVVLMVLPKLQEMSPTLIDAARDLGASRWQVLTGVVLPFIKPGIFAGFFMALTYSLDDFAVTFFVTGNGFSTLSVEIYSRARQGISLSINALSTLIFLFTMLLVAGYYFLTRRSGTGAQAAAGRGGAARGAAKEGTP
>NZ_CP045802.1|WP_101808592.1|1094740_1095817_+|ABC-transporter-substrate-binding-protein
MKSLIRSFAAILVVALGCLYLTSWLNSSQGYSGANTLTIYNWGDYIDPELLEEFQKETGITVIYQTFDSNEAMMTKIQQGGTTYDVAMPSEYAIDKMKQEGLLLPIDHAKLPNLKHIDERFLDLRFDPGNGYSVPYFWGTVGIVYNPELVPDGLVFDSWDDLWDPRLGNGLMLVDGAREVIGFGLNSLGYSLNDTNEAHLQEALAKLQKLTPNVKAIVGDEIKMLLANEEATAGVVWSGDAAEIMDENDKLDYVIPKEGSNVWFDNMVIPRTARNLDGAYRFMDFMLEPEHAARNAEYVGYSTPNKDAVPLLPEEIRSDERFYPPPQLTSRLEVYDNLGKRMLSHYNELFLEFKMHRK
>NZ_CP045802.1|WP_153782884.1|1096001_1096721_-|glycosyl-hydrolase
MKKTTRLTAFLSVLIGSLLLSATAFAAVWTSSAQWGSWSNGGYTVYNNIWGSGAGTQTIWADSYSKWGVTANHPNTGGIKSYPNSTRPINTQLAALSSLKSSFNVTVPSSGSSFVAAYDIWSGNNAHEIMLWMNKQGAVGPIAGSWDSNGNPVANFTNVSVGGHTWNVYKGSNGSNDVFSFVRTSNTSSGTVDVLAILNWCKSKGWMGNEIVNSVQFGYEITSAPNATFTTNSYSVSFS
>NZ_CP045802.1|WP_028598078.1|1097058_1097634_-|transcriptional-regulator
MNDKFAGLEPDQEQAIHKARKRVIESIGKNMDLYGITQSTGLLYGLMFFQDKPMNLDEMGQAMEMSKTSMSTGIRTLVDLNMVNKVWEKGSRKDLYEVERDWHQTFADFFVLKWRKAVEMNLTALRRSQNELVKLAEGASAETAEPVRAAVAGDLDKIGQAIAYYLWLDRVIDLLESGGIYEHVPKEPDSD
>NZ_CP045802.1|WP_101808594.1|1097882_1099103_+|glycine-betaine/L-proline-ABC-transporter-ATP-binding-protein
MPIIEVKDLTKVFGEDPKRISALLGQGWSKDRIFNETKHTVGVNRVSFSVEPGEIFVIMGLSGSGKSTLVRLLNRLIEPTSGMIEIDGQEITRLGADQLRTVRQKKISMVFQKFALFPHRTLLENVEYGLEVQKVPKAEREPKAREALKLVGLETRADSYPDELSGGMQQRVGLARALANDPDILLMDEAFSALDPLIRKDMQDELLDLQDTMKKTIVFITHDLDEALRIGDRIALMKDGAIVQIGTPEEIMVNPASEYVERFVEDVDLSKVLTAAHVMRRPETIGIDRGARVALQLMRESGISNLFVTDRSRRLIGVLTAEDASEAARRGLPLEDIVIRDAPTVAPGVLLNELFELVGSSKVPVAVVNETGRIVGVIVRGAVLGALAGHVPGREVDGDASETSAG
>NZ_CP045802.1|WP_028598076.1|1099077_1099923_+|proline/glycine-betaine-ABC-transporter-permease
MLPKLPLDKWVDAAVDWIESSLGFVLDPIAAGIEGAVEGISYVLHLLPALAMIVLLAALAWRFMRWKMALFTLVGLFLIDNLGYWDHTMDTLALVLTSAIVSIVIGIPIGIACARSKRTQQIVTPILDFMQTMPAFVYLIPAVTFFNLGVVPGVIASVIFAVPPTIRLTNLGIRQVPADLVEAADSFGSTPAQKLVKVQLPLAVPSIMAGINQTIMLALSMVVIASLIGAQGIGADVYRAVSQIKTGKGFEAGLAIVILAIFLDRLTQHLVKGKRQADRRG
>NZ_CP045802.1|WP_153784659.1|1099941_1100853_+|glycine/betaine-ABC-transporter
MKTLGTAAIATALVLAGCSSNGNEGANAGGEASGSGGSGSIGAAVGHKIIGIDPGAGLMAAADRAVTDYGLTDWTLVEGSSAAMAVALDKAVKNEDPIIVTGWTPHWMFAKYDLKYLDDPKKSFGEDEEIRTVARLGLKEDAPSAYEFLDRFEWTDADMAKVMAAVQEGAEPADAAAAWAEDNAAMIDGWVDGIEPGAGETIKLAYVAWDSEIASTNVVGWVLEHRLGYKTELMQVEAGPMWAGVAGGDADAMVAAWLPITHKDYAEQYEGKYEDLGANLKGTKLGLVVPSYMDVSSIEDLAG

Crispr_ID: NZ_CP045802_8

• CRISPR_ID: NZ_CP045802_8
• CRISPR_location: 1263427-1263503
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_8

Consensus_repeat	Method
GGAGGCCGTAACCCGATTTTTTCGGG	CRISPRCasFinder

spacers of NZ_CP045802_8

>8.1|1263453|25|NZ_CP045802|CRISPRCasFinder
CTACAGCTTTGGAATCGCGCTCGGT

CRISPR arrays and Neighbor proteins around NZ_CP045802_8

CRISPR arrays

The CRISPR arrays of NZ_CP045802_8

>merge|NZ_CP045802|8|1263427-1263503|CRISPRCasFinder
GGAGGCCGTAACCCGATTTTTTCGGGCTACAGCTTTGGAATCGCGCTCGGTGGAGGCAGTAACCCGATTTTTTCGGG

>NZ_CP045802|8|6|1263427-1263503|CRISPRCasFinder
GGAGGCCGTAACCCGATTTTTTCGGG	CTACAGCTTTGGAATCGCGCTCGGT
GGAGGCAGTAACCCGATTTTTTCGGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_101808644.1|1274067_1275711_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270298
NZ_CP045802.1|WP_101808642.1|1264033_1264609_-|dihydrofolate-reductase	unknown	unknown	gnl|CDD|223340
NZ_CP045802.1|WP_101808640.1|1258573_1259299_-|Crp/Fnr-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223736
NZ_CP045802.1|WP_101808635.1|1253006_1254698_+|iron-ABC-transporter-permease	unknown	unknown	gnl|CDD|224099
NZ_CP045802.1|WP_153782979.1|1272319_1272877_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_101808639.1|1257778_1258429_+|pentapeptide-repeat-containing-protein	unknown	unknown	gnl|CDD|224276
NZ_CP045802.1|WP_153782978.1|1271860_1272211_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379112
NZ_CP045802.1|WP_101809425.1|1251093_1251765_+|M15-family-metallopeptidase	unknown	unknown	gnl|CDD|350616
NZ_CP045802.1|WP_153782975.1|1268033_1269308_+|L-rhamnose-isomerase	unknown	unknown	gnl|CDD|179217
NZ_CP045802.1|WP_101808637.1|1255827_1256562_+|serine/threonine-protein-phosphatase	unknown	unknown	gnl|CDD|277316
NZ_CP045802.1|WP_028600378.1|1260756_1261716_+|acetylxylan-esterase	unknown	unknown	gnl|CDD|368448
NZ_CP045802.1|WP_153782974.1|1265907_1268004_+|bifunctional-aldolase/short-chain-dehydrogenase	unknown	unknown	gnl|CDD|236241
NZ_CP045802.1|WP_101808641.1|1259385_1260582_-|chromate-transporter	unknown	unknown	gnl|CDD|273350
NZ_CP045802.1|WP_101809426.1|1275810_1276692_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_CP045802.1|WP_153782977.1|1270971_1271730_+|DeoR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224268
NZ_CP045802.1|WP_101808634.1|1251895_1253002_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270265
NZ_CP045802.1|WP_101808636.1|1254694_1255822_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|226361
NZ_CP045802.1|WP_101808638.1|1256548_1257442_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|176112
NZ_CP045802.1|WP_153782976.1|1269304_1270807_+|rhamnulokinase	unknown	unknown	gnl|CDD|198349
NZ_CP045802.1|WP_153782973.1|1265343_1265757_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_101808644.1|1274067_1275711_+|extracellular-solute-binding-protein	gnl|CDD|270298	cd13580, PBP2_AlgQ_like_1, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	1.23433e-76
NZ_CP045802.1|WP_101808642.1|1264033_1264609_-|dihydrofolate-reductase	gnl|CDD|223340	COG0262, FolA, Dihydrofolate reductase [Coenzyme metabolism].	4.51523e-18
NZ_CP045802.1|WP_101808640.1|1258573_1259299_-|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].	9.08391e-41
NZ_CP045802.1|WP_101808635.1|1253006_1254698_+|iron-ABC-transporter-permease	gnl|CDD|224099	COG1178, ThiP, ABC-type Fe3+ transport system, permease component [Inorganic ion transport and metabolism].	2.06116e-67
NZ_CP045802.1|WP_101809426.1|1275810_1276692_+|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	3.05457e-131
NZ_CP045802.1|WP_101808639.1|1257778_1258429_+|pentapeptide-repeat-containing-protein	gnl|CDD|224276	COG1357, COG1357, Pentapeptide repeats containing protein [Function unknown].	1.75599e-19
NZ_CP045802.1|WP_153782978.1|1271860_1272211_+|GNAT-family-N-acetyltransferase	gnl|CDD|379112	pfam13302, Acetyltransf_3, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	4.68228e-08
NZ_CP045802.1|WP_101809425.1|1251093_1251765_+|M15-family-metallopeptidase	gnl|CDD|350616	cd14817, D-Ala-D-Ala_dipeptidase_VanX, D-Ala-D-Ala dipeptidase VanX. D-Ala-D-Ala dipeptidase (also known as D-alanyl-D-alanine dipeptidase vanX; VanX; EC 3.4.13.22) is a Zn2+-dependent enzyme that mediates resistance to the antibiotic vancomycin in Enterococci and other bacteria (both Gram-positive and Gram-negative). It is part of a gene cluster that affects cell-wall biosynthesis. The operon triggers the termination of peptidoglycan precursors by D-Ala-(R)-lactate instead of D-Ala-D-Ala dipeptides. The enzyme is stereospecific, as L-Ala-L-Ala, D-Ala-L-Ala and L-Ala-D-Ala are not substrates. It belongs in the MEROPS peptidase family M15, subfamily D.	5.47782e-121
NZ_CP045802.1|WP_153782975.1|1268033_1269308_+|L-rhamnose-isomerase	gnl|CDD|179217	PRK01076, PRK01076, L-rhamnose isomerase; Provisional.	0
NZ_CP045802.1|WP_101808637.1|1255827_1256562_+|serine/threonine-protein-phosphatase	gnl|CDD|277316	cd00144, MPP_PPP_family, phosphoprotein phosphatases of the metallophosphatase superfamily, metallophosphatase domain. The PPP (phosphoprotein phosphatase) family is one of two known protein phosphatase families specific for serine and threonine. This family includes: PP1, PP2A, PP2B (calcineurin), PP4, PP5, PP6, PP7, Bsu1, RdgC, PrpE, PrpA/PrpB, and ApA4 hydrolase. The PPP catalytic domain is defined by three conserved motifs (-GDXHG-, -GDXVDRG- and -GNHE-). The PPP enzyme family is ancient with members found in all eukaryotes, and in most bacterial and archeal genomes. Dephosphorylation of phosphoserines and phosphothreonines on target proteins plays a central role in the regulation of many cellular processes. PPPs belong to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	1.71347e-07
NZ_CP045802.1|WP_028600378.1|1260756_1261716_+|acetylxylan-esterase	gnl|CDD|368448	pfam05448, AXE1, Acetyl xylan esterase (AXE1). This family consists of several bacterial acetyl xylan esterase proteins. Acetyl xylan esterases are enzymes that hydrolyze the ester linkages of the acetyl groups in position 2 and/or 3 of the xylose moieties of natural acetylated xylan from hardwood. These enzymes are one of the accessory enzymes which are part of the xylanolytic system, together with xylanases, beta-xylosidases, alpha-arabinofuranosidases and methylglucuronidases; these are all required for the complete hydrolysis of xylan.	1.52134e-169
NZ_CP045802.1|WP_153782974.1|1265907_1268004_+|bifunctional-aldolase/short-chain-dehydrogenase	gnl|CDD|236241	PRK08324, PRK08324, bifunctional aldolase/short-chain dehydrogenase.	0
NZ_CP045802.1|WP_101808641.1|1259385_1260582_-|chromate-transporter	gnl|CDD|273350	TIGR00937, Chromate_transport_protein, chromate transporter, chromate ion transporter (CHR) family. Members of this family probably act as chromate transporters, and are found in Pseudomonas aeruginosa, Alcaligenes eutrophus, Vibrio cholerae, Bacillus subtilis, Ochrobactrum tritici, cyanobacteria and archaea. The protein reduces chromate accumulation and is essential for chromate resistance. [Transport and binding proteins, Anions].	1.98241e-98
NZ_CP045802.1|WP_153782977.1|1270971_1271730_+|DeoR-family-transcriptional-regulator	gnl|CDD|224268	COG1349, GlpR, Transcriptional regulators of sugar metabolism [Transcription / Carbohydrate transport and metabolism].	2.71986e-94
NZ_CP045802.1|WP_101808634.1|1251895_1253002_+|extracellular-solute-binding-protein	gnl|CDD|270265	cd13547, PBP2_Fbp_like_2, Substrate binding domain of an uncharacterized ferric iron transporter, a member of the type 2 periplasmic binding fold superfamily. The periplasmic iron binding protein plays an essential role in the iron uptake pathway of Gram-negative pathogenic bacteria from the Pasteurellaceae and Neisseriaceae families and is critical for survival of these pathogens within the host. This periplasmic domain (Fbp) has high affinity for ferric iron and serves as the primary receptor for transport. After binding iron with high affinity, Fbp interacts with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The ferric iron-binding proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	2.20239e-83
NZ_CP045802.1|WP_101808636.1|1254694_1255822_+|ABC-transporter-ATP-binding-protein	gnl|CDD|226361	COG3842, PotA, ABC-type spermidine/putrescine transport systems, ATPase components [Amino acid transport and metabolism].	8.50018e-125
NZ_CP045802.1|WP_101808638.1|1256548_1257442_+|LysR-family-transcriptional-regulator	gnl|CDD|176112	cd08420, PBP2_CysL_like, C-terminal substrate binding domain of LysR-type transcriptional regulator CysL, which activates the transcription of the cysJI operon encoding sulfite reductase, contains the type 2 periplasmic binding fold. CysL, also known as YwfK, is a regular of sulfur metabolism in Bacillus subtilis. Sulfur is required for the synthesis of proteins and essential cofactors in all living organism. Sulfur can be assimilated either from inorganic sources (sulfate and thiosulfate), or from organic sources (sulfate esters, sulfamates, and sulfonates). CysL activates the transcription of the cysJI operon encoding sulfite reductase, which reduces sulfite to sulfide. Both cysL mutant and cysJI mutant are unable to grow using sulfate or sulfite as the sulfur source. Like other LysR-type regulators, CysL also negatively regulates its own transcription. In Escherichia coli, three LysR-type activators are involved in the regulation of sulfur metabolism: CysB, Cbl and MetR. The topology of this substrate-binding domain is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	5.60061e-50
NZ_CP045802.1|WP_153782976.1|1269304_1270807_+|rhamnulokinase	gnl|CDD|198349	cd07771, FGGY_RhuK, L-rhamnulose kinases; a subfamily of the FGGY family of carbohydrate kinases. This subfamily is predominantly composed of bacterial L-rhamnulose kinases (RhuK, also known as rhamnulokinase; EC 2.7.1.5), which are encoded by the rhaB gene and catalyze the ATP-dependent phosphorylation of L-rhamnulose to produce L-rhamnulose-1-phosphate and ADP. Some uncharacterized homologous sequences are also included in this subfamily. The prototypical member of this subfamily is Escherichia coli RhuK, which exists as a monomer composed of two large domains. The ATP binding site is located in the cleft between the two domains. This model includes both the N-terminal domain, which adopts a ribonuclease H-like fold, and the structurally related C-terminal domain. The presence of divalent Mg2+ or Mn2+ is required for catalysis. Although an intramolecular disulfide bridge is present in Rhuk, disulfide formation is not important to the regulation of RhuK enzymatic activity. Members of this subfamily belong to the FGGY family of carbohydrate kinases.	0

Protein sequences

>NZ_CP045802.1|WP_028600378.1|1260756_1261716_+|acetylxylan-esterase
MPMLDMPLEQLRRYEGINPRPDDFDAYWERALQELDATAAEVELVPSAFQVPTADCFDLYFTGVRGARIHAKYIRPKNVPEPHAALLQFHGYSGNAGDWADKLSYASLGYSVFSMDCRGQGGGSEDRGGVKGNTLNGHIIRGLDGEPDDLLFRQIFLDTAQLARIAMDMPEVDAERIGATGWSQGGALTIACAALEPRVKRLAPVYPFLSDYRRVWEMDQAKDAYAELRNYFRLFDPQHKREQEIFTRLGYIDIQNLAPRIQGETLLGVGLMDSICPPSTQFAAYNKITAPKSLEIYPDFGHEGLPGLNDRILQFMQDL
>NZ_CP045802.1|WP_101808641.1|1259385_1260582_-|chromate-transporter
MKEENDVNPKSKPRALLELFAASTKLGLTSFGGPIAHLGYFHDEYVTRRKWIDERVYAELVALCQFLPGPASSQVGIGIGLIRAGLLGGVVAWIGFTLPSFLALTLFAFLLQGYPMDAAGWIHGLKIVAVAIVAHAIIGMGQKLTPDRNRVAIAVISATVTLSWQTAFSQVLLIVAAGLIGLLMYSKTASSDFSSLSVPVSRGTAALCLGLFASLWIALPLLRPFSNTGFLPLFDSFYRAGSLVFGGGHVVLPLLEREAVPAGWVTSEDFLAGYGAAQAVPGPLFTFAGYLGAMAFGFSGAVVATLAIFLPAFFMIIGALPFWSSLRSIPKVQGALMGINAAVVGILLAALYDPLWTTAILSPADFALAMILFVLIALWKWPPWIVVAASAAGGMMIS
>NZ_CP045802.1|WP_101808640.1|1258573_1259299_-|Crp/Fnr-family-transcriptional-regulator
MDAASGVTKPETAPGNSAAFSADSLAKLSALMRKHRIPAGGHVFWEGEPAEYWYYLEHGHVKGMKTSAEGKEFTMYRYKQGDFFGQLGFDGEPSQSFSAVAQTDCVISFIPRGELEFALWRFGGLALECIGWMSQMNRHTQTKLRDLMLYGKPGALCSTLIRMANTYGMPVDDGILITQRITNSELAETIGAARESVNRLLADYRRAGALSMRQGHIVVHDLEQLMQHCRCEGCPKEICRM
>NZ_CP045802.1|WP_101808639.1|1257778_1258429_+|pentapeptide-repeat-containing-protein
MSETRKRLKLEAPRLPAEPERLSLPARLGTRDAFEHGLVEGERLEELDADKVVFDGVVFRGVTFDSAKLRSLELTDVLFDRCDLSNADLSRAVVHRAQFRSCKLVGADLSEAMLRNVLVEDCQLDYANLRAADLKGVVFADSSLNRADFCMAKLAKTEFHRCKLDGALLGTPLRGIDLSDSEFTGLSCNPDDLRGCIISREQAFIFAALFGMVLKD
>NZ_CP045802.1|WP_101808638.1|1256548_1257442_+|LysR-family-transcriptional-regulator
MNLLKFQIVELLDKHRKITAVAEALGLKQPTVTYHMKSLEQEYGVKLFEPRMDKVILTEAGRALLHYAGKINCLASEAKRTVEEYGTPGRGTLRVGASYVPATYMLPRLLKEFAARHPKVTVTLAVKPSAVIKEMLLNHEIDLGVLSAEPFRLPMLDVRELCDDELVLAHAPSHDLAASSELTPGLLCTADFVLHGPHSSTRELTDRWLEQHGVRLEQHLELDSLEAIKQMVIQGGHVTFASGLAIQAEVARGQLLARAIPEFRHRRKISCATNRDRHHSGPLDSMMELLQGWEQIQ
>NZ_CP045802.1|WP_101808637.1|1255827_1256562_+|serine/threonine-protein-phosphatase
MSRILALSDIHGFTAEARRLLQAAAYEPGRDKLFLLGDYIDYEPCTWSSLDEIMELTAGGAVALAGNMERHLQRHLEQELESRGSLDHGSSVQLQFLKRLPLHAAAGGWLFVHAGIRPGVPLERQAERDLIGIREEFWGAAEAAEAPPMHGGGTLETSGEWLPQVQIVFGHTPTHKIGAPPGELWRGPGKLGIDTGAKHGLRLTLVDLTGRKDYSCPTSPAGPGQEQAAVAINDWEAGEGDEPA
>NZ_CP045802.1|WP_101808636.1|1254694_1255822_+|ABC-transporter-ATP-binding-protein
MTAMLEIKQVGKSYGKQEVLGSVDLSVQAGEIISVLGPSGCGKSTLLQLIAGLQQPDRGEILLRGKLAASRSAMLAPEKRGINMVFQDYALWPHMTVFENIAYGMRRSRQDQAGIKASVAELAALLRLEGLEQRLPPQLSGGQQQRVAIARALATKPDLMLLDEPLSNLDMQLRVEMRTEMAYLFKKLGTTVFHVTHDPEEAFSMADRLVIMREGAIDQIGTPQECWRRPASASAAKLLGAGNRLEVMGRIGGGVSVGEAKLAGVWPGQLAASNAEGPAQLLFRPDAADFQPHVVCTSGEAAESAASLEPAWERNRLPVHVVHSVFEGKGWRVLARTSDGQPLTFLHHRPLAAGDEGLLTISPTDLYLYPILEAN
>NZ_CP045802.1|WP_101808635.1|1253006_1254698_+|iron-ABC-transporter-permease
MKLLPSQGNRTGWLMLAVLFVLILLPLLAVVIQVLFPGIFFGTLKIGDLSLLLDIFRRPLWYASLKNSVLLGLGTTVLATLLGGALAFARSRWAFPTARLLDISVWLLLITPSFILAQGWVMFAAPDGLAAQRLGWDGASALVFQPAGLIAVMTLSKFPLAYLTVKAALQWRVERLSDAARLSGASPWTVLRTVELPLLLPAIASGAMLVFMDTVGDFGLPASIAAVFRFPTLPYSIYSALYTSPIRFDMAGALSFYLVLLIALAMSVQLYAMRKSRFDFLSSRAVESKPRRPARGGSLLALANSAFLAIAIGIPLGSNLLMSLQGDSAGGGFTLDHYRALFQGDSRLAQGLAHSLEIALTAAAIGLVVGFLTAYVLTYTSFRLKKTIDVMSLVSLAVPGIVLGIGYIFIWNQAWLQHIGLLLYGTPWILALGGVAGAIPVITRIMAGAMAQVPERLLAAAQLQGAGFFSRLRTVLAPLVKGALLSAGLTAFGSSVFDLALSSVLYPPNYMTLPVVINKAFEDLRFGYASAATLTGAGLVVLIILSVDLLARGTRRRSRRTTS
>NZ_CP045802.1|WP_101808634.1|1251895_1253002_+|extracellular-solute-binding-protein
MVRRKTVTALLALSLSLAVSACGAQNASQNAAGPAAEGQAPAGTEASTAPEASTAPSKSDEPLVVYLNDFDEIIQPMFEQATGYKLELVSGNGAELASRIEAEKGNPHWDVVWMDSMPLIDQLGKTGRLLEGWTPADIGNLTDFASGLVPANGTYYPTGAHAAAVIAYNTKAFTKDTAPKTWADLADAKFKNALGMADPAVAAPAYPFVSYFFQSQGMDAAKGYFDSLFKNGMHVYPKNPNVAKALTGGEIKAAALQESNAYALKNKGEPVDIIWPAEGAPASVRVAAIQKETKHLEAAKAFVEFLLDPKTQQALIDKGEESYFEPSAKGVNAKADRAGDAKLVLAEAAWAGEHEGEIKQWFADKAVK
>NZ_CP045802.1|WP_101809425.1|1251093_1251765_+|M15-family-metallopeptidase
MSPKPASPKEEKKPVPERKRKLPSGFVYVDEVIPTAQYEIRYFTDYNFVGARLDGYNAPYAILTKQAAEALKEAHDFLAPKGYGLKIFDAYRPAKAVRQFVAWSKDASDQRMKEEFYPEVDKAKAFKLGYISSRSGHSRGSTVDLTLFERKTGKEADMGSPFDFFGDISSHGTPEIGKAPAERRALLKRAMELAGFKPYSKEWWHYTLEKEPFPKKYFDFDIE
>NZ_CP045802.1|WP_101808642.1|1264033_1264609_-|dihydrofolate-reductase
MRKLVLFLHASLDGFVEGPNGAMDIGWVSYDAHLEKHAKEILSTADTVIWGRGTYEMMYGYWPSVPSDPSASQHERDHAEWIEKTTKIVFSTTLDKVEWANSRLVKEEVREAILALKQQPGKDMVILGSPRLAHRLMQLDLIDEFKITVSPVLIGKGLPLFQGIEEKISLELVENKTFDSGAIGLVYRRAR
>NZ_CP045802.1|WP_153782973.1|1265343_1265757_+|hypothetical-protein
MKAELASHLAALFVAPLLASIGISLFLLEPAALIYVLLISWIGTLCVAMPVSWMIGRIVGKKDGPGRALLSVLLHGAAGGALMLAFTALAEPGPPGPLATGGFGWLFVLSGAANGFAYGLIRLAVRSLVIGREPFQK
>NZ_CP045802.1|WP_153782974.1|1265907_1268004_+|bifunctional-aldolase/short-chain-dehydrogenase
MVQSLWNQEAAEKAAKEQNGSLEGLAGLVYRSNRIGADRSVCNWGGGNTSTKTTVKDFRGREIDVMYVKGSGSDLASMTARNFTGLRLDDVLELREREAMSDEEMVAYLGHCMIDASHPRASIETLLHAFLPFKHVDHTHPDAIISLCCADNGRELAAEIFGERFVWVPYIRPGFTLSKMIADGVRANPNAELVLMEKHGLVTWGDTQEACYEQTIRIISEAEAFIEARVDGSRLFGGLKSAPLPETDRRRVAAAVMPLIRGLVSDEKRMVLSFDDGDDILAFAGGADAPQLSQVGAACPDHLVHTKVVPLLADWTPDSSEAGIAALQAALRQGIEAYKENYKAYFERNKNEGDRRFEAAPRVILIPGVGMVNTGKSLASARVSGALYHRAVAVMRGATALGRFVSLSENESYNVEYWPLELYKLSLAPAEAEFSRQIAFITGGAGGIGSETARRLAEGGAHLVLADLNLEGAQKVADDINARFGEGRALAVRMDVTSEEQVAAAFAETALAYGGVDILVNNAGLATSSPFEETTLKEWNLNMNVLGTGYFLVAREAFRQMKEQARGGSMVFIGSKNSVYAGKNASAYSAAKALEAHLARCIAAEGGELGIRVNTVLPDAILQGSAIWNSSWREERAAAYGIEPDQLEDYYRQRTTLRVNIYPRDIAEGIAFFASARAEKTTGCMLTVDGGVPAAFTR
>NZ_CP045802.1|WP_153782975.1|1268033_1269308_+|L-rhamnose-isomerase
MNPTVKQSYELARAQYAAHGIDTDEALERLSRIKLSVHCWQGDDVRGFLFREQELSGGISVTGSYPGAARTPQELRADLERAFSLIPGKHKVNLHAIYADTEEAVDLNELEPKHFQRWVDWAKEQGLGLDFNPTCFSHPKAADGFTLSHPDEAVRRFWIEHCQASRRIGASFGEQLGQPCVTNVWVPDGYKDVPADRLAPRRRLKEALDEVFAEPLDPAHHLDAVESKLFGLGSEAYVVGSHEFYMGYGLQNDKLICLDSGHFHPTETISNKLSSLSLFASGILLHVSRPMRWDSDHVVILDDELLEIARELVRGDLLERTFIGLDFFDGSINRVAAWVIGTRSTLKALLRALLEPAEALRQAELDGDYTTRLALAEEFKSYPFGAVWDYYCERSGVPAREAWLDDVKAYEREVQLPRGEAARV
>NZ_CP045802.1|WP_153782976.1|1269304_1270807_+|rhamnulokinase
MTTRLAFDLGAGSGRAVLGRLGGSRMELTEVHRFANEPVQAGGGLYWDILRLLHELKQGLRLAAREGGAPPASLAIDSWAVDFGLLGRDGTLLGNPLHYRDRHAEGMMERLRERYGDEWLFRRSGLQFLPFNTIYQLAAMGERRSPQLRQAQTLLMIPDLLRYFLTGEKKQEFTNATTTGLLNPSARQWDNELLKAAGVPVRLFAPLAQPGDAAGELTTAVQAELGLSAQVQVLCAAEHDTASAVVAVPAREESFAYLSCGTWSLMGTEVPEPVLSEQALAYNFTNEGGAAGTWRLLKNIMGLWILEELRREWQREGHCPGYEELLAGAGALPAGGPLIDPDDPLFLPAGPMGPRIRQWCRESGQPEPQGYAGHARCILESLALQYRYVLKQTELVSGRSFSGLHMVGGGIRNRLLCQWTADSIGRPVWAGPAEGSAIGNLAVQWISAGELSGLSEARRVIGDSFGVETYEPAPGSGERMAEAYGRLQALKDKRKGRRSG
>NZ_CP045802.1|WP_153782977.1|1270971_1271730_+|DeoR-family-transcriptional-regulator
MLAAERYEQIVQLVNERGSIRVTELSELCRVTEETIRRDLDRLEQEGRLRRSHGGAVSVRDAQPETPFAEREVTFAAQKRRIAAEAARQVRPRERILLDASSTAWYMARELPDMPLTVLTNSARVAVELAAKEQIQVICTGGQLSRASLSFVGPSAERSLEEYHVDKAFLSCKGLHVERGLSESNELQARVKQQMLRMADEVVLLADASKIGLQSFTRFGSLEQVGRLVTDDRITAEAAQALRESGVAVVVV
>NZ_CP045802.1|WP_153782978.1|1271860_1272211_+|GNAT-family-N-acetyltransferase
MLDSQVRMAIEFEGRLIGYADLAQIRTNAAELGIAIGESGLWGKGIGFLAAGRMIELAREKYGITLFNAETNEENARSRTMPEKLDFVEISRVGREAYLGKDGRLIQYRLGPVIEQ
>NZ_CP045802.1|WP_153782979.1|1272319_1272877_+|hypothetical-protein
MKKRLWLVMAAAVLIAAGLFYAFHEREMDRKSAELAEIKNHVAAAAVSSMMSNAAFLDSFLPEASNPSSAKMKLDDRFLACFVAFSNLGQLSLQMETIDESDHEAWREIRLGFEKASKLMAGLERSEMDREIYLARINEFATVFLDGMTHMNRNTSTIPHHELNKIREAAIQFNAESFWEILSKT
>NZ_CP045802.1|WP_101808644.1|1274067_1275711_+|extracellular-solute-binding-protein
MKKTTMLLSATMAMALLAAGCSGGNGNGNGNEGAAAGTDNNAQNAAGSGGEAEAPKEPFTIKMALMAGPKTPDSWAEKALEGELEKSMGRKVDVQPIFLPDWSELNTKINLLMSAKDTRPGILWTGDTKEYTKWVDAGIAQDVTPSLQKYGKEILDYYRKDTLFYHWDKSGKIFRIPGDVPEASYMTTIVRKDWLDKLGLQAPKTLDEYVEVLRAFANGDPDGNGKKDTYGISGDNYYRSLAPFFYANGLDVENFVKNADGSIQFGALDPKVKDVLKLLSELYKEGVMDPRMTTSANNDDNKVNDIYASGKVGSFYRWVDYFNPGNSVNISFKKLNPDGEYISIAPIQGPDGFSSDLPDPGIGWCYLVVTDATDVDSAVQVLNTMATPEVFKTITFGNEGEHYKMDGGIFTPTIQPEEGSKLGLGNFGWYIQRKDAANIKNTPEVTKMFEEKIATSQPMRDKIVVFKAIDRPEWDRYSADVKKVRDELFWGIITGKTPLDAFDKWPAQYEKLGGKKIDEEAAGLFEKQQAEHVEYDKWYEENITPYK
>NZ_CP045802.1|WP_101809426.1|1275810_1276692_+|sugar-ABC-transporter-permease
MRDRYLYLLLLPGLLLVLVFKYMPMYGVIIAFQEYNIYKGITGSEWVGFDQFTRLFNSPDFTEILGNTIIISVYKLIASFTLPIILALLLNELRSKLFKRFAQSVVYLPHFISWVIFSGILITFLNPVDGLVNLILQRFGVMPIDFLGDVRYFRSILVISDIYKEVGWGTIIYLAAIAGVSADLYEAARIDGANKLKQTWHVTLPAIRPVILILVILSLANILEAGFQQIFLLYNPLVYDVADIIDTYVYRVGIQEANYSYATAAGLFKSAVAMTLILTVNTIVKKSGQEGLW

Crispr_ID: NZ_CP045802_9

• CRISPR_ID: NZ_CP045802_9
• CRISPR_location: 1295925-1296080
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_9

Consensus_repeat	Method
TGAGCCGACGGAGGCACGCGGCAGCCGGTGCTGGATGAGCCGACGGAGG	CRISPRCasFinder

spacers of NZ_CP045802_9

>9.1|1295974|58|NZ_CP045802|CRISPRCasFinder
TACGCGTCAGGTGGAGCTGGATGATCCGGTCGTAGGGAGGCGGAAAGGCGGAGCCGAA

CRISPR arrays and Neighbor proteins around NZ_CP045802_9

CRISPR arrays

The CRISPR arrays of NZ_CP045802_9

>merge|NZ_CP045802|9|1295925-1296080|CRISPRCasFinder
TGAGCCGACGGAGGCACGCGGCAGCCGGTGCTGGATGAGCCGACGGAGGTACGCGTCAGGTGGAGCTGGATGATCCGGTCGTAGGGAGGCGGAAAGGCGGAGCCGAATGAGCCGACGGAGGCACGCGGCAGCCGGTGCTGGATGAGCCGACGGAGG

>NZ_CP045802|9|7|1295925-1296080|CRISPRCasFinder
TGAGCCGACGGAGGCACGCGGCAGCCGGTGCTGGATGAGCCGACGGAGG	TACGCGTCAGGTGGAGCTGGATGATCCGGTCGTAGGGAGGCGGAAAGGCGGAGCCGAA
TGAGCCGACGGAGGCACGCGGCAGCCGGTGCTGGATGAGCCGACGGAGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_153782994.1|1297507_1299034_+|iron-sulfur-cluster-binding-protein	unknown	unknown	gnl|CDD|224062
NZ_CP045802.1|WP_153782987.1|1286334_1286715_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|379233
NZ_CP045802.1|WP_153784676.1|1308972_1310112_+|AI-2E-family-transporter	unknown	unknown	gnl|CDD|223701
NZ_CP045802.1|WP_153782990.1|1291785_1292775_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|223521
NZ_CP045802.1|WP_153784675.1|1299299_1299968_+|lactate-utilization-protein-C	unknown	unknown	gnl|CDD|376839
NZ_CP045802.1|WP_153784674.1|1290787_1291771_-|dipeptide-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|236898
NZ_CP045802.1|WP_153782988.1|1287104_1287998_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|224094
NZ_CP045802.1|WP_153782989.1|1288009_1289014_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223674
NZ_CP045802.1|WP_028597852.1|1296782_1297511_+|(Fe-S)-binding-protein	unknown	unknown	gnl|CDD|223325
NZ_CP045802.1|WP_028597858.1|1302978_1304565_-|peptidase-M4-family-protein	unknown	unknown	gnl|CDD|225768
NZ_CP045802.1|WP_153782991.1|1293360_1294011_-|DUF2306-domain-containing-protein	unknown	unknown	gnl|CDD|370803
NZ_CP045802.1|WP_153782998.1|1304985_1305708_+|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|379312
NZ_CP045802.1|WP_153782995.1|1299995_1300706_+|FCD-domain-containing-protein	unknown	unknown	gnl|CDD|225097
NZ_CP045802.1|WP_153782992.1|1294144_1294654_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224759
NZ_CP045802.1|WP_153782986.1|1285516_1286224_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153782997.1|1301858_1302806_-|catalase	unknown	unknown	gnl|CDD|163709
NZ_CP045802.1|WP_101809427.1|1289020_1290661_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|173858
NZ_CP045802.1|WP_153782996.1|1300751_1301732_+|gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_CP045802.1|WP_153782993.1|1294643_1295894_+|MFS-transporter	unknown	unknown	gnl|CDD|341042
NZ_CP045802.1|WP_153782999.1|1305825_1308540_-|aconitate-hydratase-AcnA	unknown	unknown	gnl|CDD|236445

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_153782994.1|1297507_1299034_+|iron-sulfur-cluster-binding-protein	gnl|CDD|224062	COG1139, COG1139, Uncharacterized conserved protein containing a ferredoxin-like domain [Energy production and conversion].	0
NZ_CP045802.1|WP_153782987.1|1286334_1286715_-|helix-turn-helix-domain-containing-protein	gnl|CDD|379233	pfam13518, HTH_28, Helix-turn-helix domain. This helix-turn-helix domain is often found in transposases and is likely to be DNA-binding.	7.87423e-05
NZ_CP045802.1|WP_153784676.1|1308972_1310112_+|AI-2E-family-transporter	gnl|CDD|223701	COG0628, yhhT, Predicted permease, member of the PurR regulon [General function prediction only].	1.6287e-66
NZ_CP045802.1|WP_153782990.1|1291785_1292775_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	0
NZ_CP045802.1|WP_153782995.1|1299995_1300706_+|FCD-domain-containing-protein	gnl|CDD|225097	COG2186, FadR, Transcriptional regulators [Transcription].	1.75513e-52
NZ_CP045802.1|WP_153784674.1|1290787_1291771_-|dipeptide-ABC-transporter-ATP-binding-protein	gnl|CDD|236898	PRK11308, dppF, dipeptide transporter ATP-binding subunit; Provisional.	4.46463e-158
NZ_CP045802.1|WP_153782988.1|1287104_1287998_-|ABC-transporter-permease-subunit	gnl|CDD|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.68603e-115
NZ_CP045802.1|WP_153782989.1|1288009_1289014_-|ABC-transporter-permease-subunit	gnl|CDD|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	6.00891e-136
NZ_CP045802.1|WP_028597852.1|1296782_1297511_+|(Fe-S)-binding-protein	gnl|CDD|223325	COG0247, GlpC, Fe-S oxidoreductase [Energy production and conversion].	1.32599e-55
NZ_CP045802.1|WP_028597858.1|1302978_1304565_-|peptidase-M4-family-protein	gnl|CDD|225768	COG3227, LasB, Zinc metalloprotease (elastase) [Amino acid transport and metabolism].	9.91958e-163
NZ_CP045802.1|WP_153782991.1|1293360_1294011_-|DUF2306-domain-containing-protein	gnl|CDD|370803	pfam10067, DUF2306, Predicted membrane protein (DUF2306). Members of this family of hypothetical bacterial proteins have no known function.	2.15939e-28
NZ_CP045802.1|WP_153782998.1|1304985_1305708_+|methyltransferase-domain-containing-protein	gnl|CDD|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	2.8854e-25
NZ_CP045802.1|WP_153782992.1|1294144_1294654_+|MarR-family-transcriptional-regulator	gnl|CDD|224759	COG1846, MarR, Transcriptional regulators [Transcription].	1.20466e-17
NZ_CP045802.1|WP_101809427.1|1289020_1290661_-|ABC-transporter-substrate-binding-protein	gnl|CDD|173858	cd08493, PBP2_DppA_like, The substrate-binding component of an ABC-type dipeptide import system contains the type 2 periplasmic binding fold. This family represents the substrate-binding domain of an ATP-binding cassette (ABC)-type dipeptide import system. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	0
NZ_CP045802.1|WP_153782997.1|1301858_1302806_-|catalase	gnl|CDD|163709	cd08153, srpA_like, Catalase-like heme-binding proteins similar to the uncharacterized srpA. Catalase is a ubiquitous enzyme found in both prokaryotes and eukaryotes involved in the protection of cells from the toxic effects of peroxides. It catalyses the conversion of hydrogen peroxide to water and molecular oxygen. Several other related protein families share the catalase fold and bind to heme, but do not necessarily have catalase activity. This family contains uncharacterized proteins similar to the Synechococcus elongatus PCC 7942 periplasmic protein srpA, of mostly bacterial origin. The plasmid-encoded srpA is regulated by sulfate, but does not seem to function in its uptake or metabolism.	5.78278e-94
NZ_CP045802.1|WP_153784675.1|1299299_1299968_+|lactate-utilization-protein-C	gnl|CDD|376839	pfam02589, LUD_dom, LUD domain. This entry represents a domain found in lactate utilization proteins B (LutB) and C (LutC), as well as several uncharacterized proteins. LutB and LutC are encoded by th conserved LutABC operon in bacteria. They are involved in lactate utilization and is implicated in the oxidative conversion of L-lactate into pyruvate.	2.58261e-27
NZ_CP045802.1|WP_153782996.1|1300751_1301732_+|gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	1.37086e-64
NZ_CP045802.1|WP_153782993.1|1294643_1295894_+|MFS-transporter	gnl|CDD|341042	cd17489, MFS_YfcJ_like, Escherichia coli YfcJ, YhhS, and similar transporters of the Major Facilitator Superfamily. This subfamily is composed of Escherichia coli membrane proteins, YfcJ and YhhS, Bacillus subtilis uncharacterized MFS-type transporter YwoG, and similar proteins. YfcJ and YhhS are putative arabinose efflux transporters. YhhS has been implicated glyphosate resistance. YfcJ-like arabinose efflux transporters belong to the bacterial MdtG-like and eukaryotic solute carrier 18 (SLC18) family of the Major Facilitator Superfamily (MFS) of transporters. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	9.91891e-63
NZ_CP045802.1|WP_153782999.1|1305825_1308540_-|aconitate-hydratase-AcnA	gnl|CDD|236445	PRK09277, PRK09277, aconitate hydratase AcnA.	0

Protein sequences

>NZ_CP045802.1|WP_153782993.1|1294643_1295894_+|MFS-transporter
MSAEPLTLRKEPLWTRSFIVLTLGAFLMFLCLQMLMSPLPSYVEERFAPGPFVISLVTSLFALAAIAARFATAWMLGRISRNIVLFAGLAVSALATLGFSAVSGIEALLALRVLFGIGFGMASTVLPTLVTGIIPPRRMGEGVGYFGLSSSMAMSLGPMIGLSIMDGLGFRALSLAGAASSLVIIPLLLVFRAIPPVRVRVPAAAIGGTAAERASVGSAAAGAREELGRSEAGPAWLPALLNTLMAVTYGGLLSYLVLFGREMGLPNIGLFFLLNAVAILLVRPIAGRLFDRFGHLAVLPAASLLLMGGLLLLSWSDTTGLLLLSALLYGLGFGSIQPTAQAWMLRSMPVARQASANSLFYNSTDLGVAVGSMLLGAVAAATGYAVMYRWAALSMALLLAVYGAGLALGRRRARRA
>NZ_CP045802.1|WP_153782992.1|1294144_1294654_+|MarR-family-transcriptional-regulator
MHASEDLTHPRSGPASGAGLDDSIGFLLGAAYRKVSLTLLQQLRDWDITPEQWSMLARICERGGRIQRELGELTGKDKPTTTRILELLEAKGLIVKQPDPKDRRSQRIHATAQGERLLAETRPVERKALDIGLRALTEEDRAQLRQLLQRIVQPPASSLAEAQEEADER
>NZ_CP045802.1|WP_153782991.1|1293360_1294011_-|DUF2306-domain-containing-protein
MSSKAALRWLAAAAAAAVAYVLYKSYLADPQAAGFLALKPPGQGPDKLGSWLAVLQVHIAAACAATACGLLGFAPAGRRTPRRLNLHRWNGYLYFICVFLVCLTSGYMAPYATGGKWASVPFNLLNMLWPAITLLAILRARKRRLAAHKRLMIRSYAFCFNNMTLHLFTGLFTGLLELPYAAGYAAALYANIAFLLLAGELAIRMLRVPRDEGGRA
>NZ_CP045802.1|WP_153782990.1|1291785_1292775_-|ATP-binding-cassette-domain-containing-protein
MAPSLLELTDLHTHFATDRGELPAVDGIDLTIRSGEIVGIVGESGCGKSVTSLSIMRLLPEPLARYAGGSIRFKGEDLLRAKEKRMKQVRGNEISMIFQEPMTSLNPLLTIGEQIGETLRVHRPVGRKDAAAKAVEMLRKVGIPRAEGVAKAYPHQLSGGMRQRVMIAIALCCEPELLIADEPTTALDVTIQAQILDLMKTLNRETGTAIMMITHDLGVVAELCERVVVMYAGKIVEEGSVHDILTDPRHPYTQGLIRSIPRLDEERERLYSIPGQVPRPGAIAQGCRFAPRCEHAMPICGEQLPELIAGARPAHRSRCWLNTAQEVAN
>NZ_CP045802.1|WP_153784674.1|1290787_1291771_-|dipeptide-ABC-transporter-ATP-binding-protein
METTPQAEALLEVEELRTHFPIRSGLLQRVSGHVKAVDGVSFQVRRGESFGIVGESGCGKSTTGRSLLRLLEPTSGRVRFDGEDFLALKDEALRRKRRDMQMIFQDPFASLNPRHRIGKILEEPLIVHGIGSAAERRERVARTMETVGLSAWQLDRYPHQFSGGQRQRVAIARALMLEPKLIVADEPVSALDVSIQSQILNLMQDLREQMGLTYVFIAHDLSVVKHFCDRVAVMYLGRVVEIADKRGLYREPRHPYTKALLSAAPSPVPGAAAERIVLQGDVPSPANVPEGCVFHTRCPVAMDVCRSQRPPLKIDGEGHGTACHLYP
>NZ_CP045802.1|WP_101809427.1|1289020_1290661_-|ABC-transporter-substrate-binding-protein
MLLAATLAFAGCSGNSNAPAAQNGGATGSPAPTTSTAPSDGAASSQDTLIVARGGDSAALDPAIVTDGESTKVTEQIFEGLLSYKPGTTEVQPALAESYEVSDDGLTYTFKLRQGVKFHDGTDFNADAVVFNFNRWSDPNSPNKYEGDSFYYYDSMFGPEGSRVIKEVKAIDPATVQFTLNKPQAPFLQNIAMPSFGIASPKAVEEKKDKFKSEPVGTGPFVFKEWKRSESITVEKNPNYWQSGLPKLARVIITVIPDNSARLTALQNGEIDLMEGVNPDDLGTLESNAELQRIERPSFNVGYVGFNLKKKPFDDPKVRVALSHAVNKEGIISAFYAGLAEAAVNPMPPSTLGWNADVKDYPYDLEKAKQLLADAGYPNGLPEEMVFYAMPVARPYMPDGKKVAEAIQADFAKIGVKTRIESPEWATYLDDAKDGEKDDLFMLGWNGDNGDPDNFLFTLLHKDTIGSNNYSFYSNEEVNKLLSEGQAETDPAKREELYKQAQVLIKQDAPWIPLVHSTPLLAGKANLKGYVPSPTGGEPYSEVYFE
>NZ_CP045802.1|WP_153782989.1|1288009_1289014_-|ABC-transporter-permease-subunit
MLNYAIRRLLMLVPVLLGMTVIVFMIIRAIPGDPAEVILGEKASPQSKEALRQELKLDEPLYVQYGDYLGKLLSGDLGKSIRSKEPIATEIGPYLAATLELTAFAMLFAIVVGVNAGIVSAWRQNSWFDYASMLIALVGVSMPIFWLGLMEQWIFALELKWLPSIGRANPRDPVDAVTGLYLIDTLVAGRFDQFGTVLKHLVLPGVALGTIPMAIIARMTRSSMLEVMRSDYIRTAKAKGLSQLALIYKHALRNAFIPVLTVIGLQFGLLLGGAVLTETIFAWPGIGRYIFDAISSRDYPVIQSGILIIAFLFVLINLLVDLLYAAVDPRISYK
>NZ_CP045802.1|WP_153782988.1|1287104_1287998_-|ABC-transporter-permease-subunit
MSQPAVRLPVPLPKPEEASSPWRDAWRSFRRNRMAMAGLGIIVFFILVAALAPVIAPYDYKEQELMNRLQPPGGEHWLGTDDLGRDILSRLIHGARISLWVGVSSVAGSIVAGTMLGILAGYYGRWWDAIISRLFDILLAFPGILLAIAIVAALGPSLQNALLAIAIVNVPVFGRLVRAKVLSLREEEYIVAARSLGMKSSRILLQHILPNSLGPIIVQGTLGIATAIIEAAALGFLGLGAQPPDPEWGKMLSDSRQLIQKAPWTVLFPGLAIMLTVLGFNLIGDGLRDVLDPRMKR
>NZ_CP045802.1|WP_153782987.1|1286334_1286715_-|helix-turn-helix-domain-containing-protein
MKQHRSTSGEVRTQVVRESLDGVPTAELARKYAVSQRSVRAWMREYQEKAALANKSTASTASTGARPDNAQRLAEMEAKYEQVQKLLAEKELESEILRALINTKTNSPASMNDSKSRNHSSGRGNR
>NZ_CP045802.1|WP_153782986.1|1285516_1286224_+|hypothetical-protein
MDFSRHAGHRRGQSFDSAHAAWLQRHVDARTGERKDRLRRGHAHGEILFLRAVWWPLFGHFDDLHPEYEVKDWRGAACYLDFAWFAEGVRFNIDVKGFGPHVQQMDRSGYRREAMREMFLHSHGFRTLTVAYDSLKEEPDQVRDLIAQIARSGSDFSVGIKGDGAGEGMNRVDAALLRYARVHGGDIYPFKAAEAIGVHRRTAAIHLKRLAEKGLFESVAAGGKVCRYRLRPNLA
>NZ_CP045802.1|WP_028597852.1|1296782_1297511_+|(Fe-S)-binding-protein
MKVSLFITCLSDAIYPRVGEAMARILARQGVKLDFPKVQTCCGQPAYNSGYWDEARKTARTILAAFRDSDFVVSPSGSCTYMVHHYEELFKDEPEALREARELRSKTYEFTQFLVQVLGVTDIGARFPHKVTYHPSCHGSRLLGVKEEPLELLRGVDGLQLVPLPFAEDCCGFGGTFAVKMADISGAMVTEKADHVKETEAEVLVGLDMACLMNIAGNLRRRGEPVRVLHLAELLEEGARVG
>NZ_CP045802.1|WP_153782994.1|1297507_1299034_+|iron-sulfur-cluster-binding-protein
MIKEQAKPAQPDTVRERAGLALNDEFLRQAVKFTTERLRSGKKAASEAHGHWDEWREQGRQIRLHTIAHLDYYLNLFADNARANGVHVHFASTAEEAVSLSLAIAESAGARSVVKSKSMVTEELHLNHALESIGVEAVETDLGEYIIQLAGETPSHIIIPAIHKNRYQIAELLSAEAGETLPPDTTILAGFVRRKLREKFLEADIGMTGCNFAIAETGSMVLFENEGNARMVSTVPKTQITLMGMERIIPSWEDLETMATLLPRSATGQRLTVYMSGITGPKRADDADGPEEMHLIILDNGRSNQLGDPEFQELLNCIRCGACLNACPVYRHIGGHAYGGTYSGPIGAVLTPALKSNVAEWDDIASASSLCGACYEACPVKIPLHDMLVSLRRRKVEAGRADALETLGMKGFGAVAGRAGLMGAALGAGRLGQRLVARGGEIRLRLGPLKGWNKYRVTPTLAKQPFRKRWSTLEQELTGELREMDPAVKKRLEELARRGGRKGGDSHG
>NZ_CP045802.1|WP_153784675.1|1299299_1299968_+|lactate-utilization-protein-C
MDGIAAKLGRPRQLERPVQPRRGAPAFWREFQWSPEERAAKLREHFEAAGGKLAELPDLEAAGRFIAEQAREMKARRILRQDEAELARLGLEPALEPEGCEVRVWNEDGGGRESWLPRAAEADFGVVLADGAAAYTGSVCVRSAPHKGRSVSLLPTALFVVLPRERLATRLGELLLPLDEAGREAMPAGVHFISGPSRSADIENDLTIGVHGPGIVTILLIG
>NZ_CP045802.1|WP_153782995.1|1299995_1300706_+|FCD-domain-containing-protein
MEVKPLNKQNHYEAIAGQLRRLIDDGSVKPGDKLPSARELSERFGVGRSTMREALSALKAMGYIDIRQGGGSVVRPPEERAGGLPPLLAAAGATREELLELLEARRSLELANVALAARKRSADDVARLRELAEGMSGTLGDDLEGERYDMEFHLALAHATGNRMMARLYESLMAPIERAIRAVRRTELYASREVAGRLADAHVRILLAVEAGDEALAAAEMQAHLEHVERIVMKHL
>NZ_CP045802.1|WP_153782996.1|1300751_1301732_+|gfo/Idh/MocA-family-oxidoreductase
MEGKKTIRWGIMGPGGISEGFAKDLAHAQGAELAAVAGRDPDKTAAFAGKFGIAKTHGSIEELAADPEVDIVYIGTVHPVHKEHALAALAAGKPVLCEKPLAMNAAEAREIAGLAESKGVFVMEAMWTRFLPAIRQARRWLDEGAIGEVRLLKAEFGFDAGWNPDGRLLNKDLGGGTLLDAGIYPVSFASFVFGEQPERIESVARIGETGVDEQFSLLLGYGDGRAASLHGSIRLEMENDAWIYGTKGRIRIPGFLWSRGAELRVKGEEPVVFEDGRVCNGYAFEAEEAMDALREGRTSSEIMPIAESVRILETMDRIRAQWGLTY
>NZ_CP045802.1|WP_153782997.1|1301858_1302806_-|catalase
MTAPKEPMPSPAELPARSIDAIEELAGSHPGQRRAHARGICARGVFTPSGEAARLTGAAHLQREPSDVVVRFSNSASDPATRDLLSPAKGMAVQFQRPDSAGVKPVIVAVTASVFVARTPESFLEMMLAARDLARDGLSVKERLKSLLGSFPHAGEALTILSELKPPASFASVPYHSIHAFYLVDGEGRKQPVKYEWIPDAEVAYLPLLKTAVASKDYLEDELRERLEKLPAGFTLRIALGEPWDPVDDSSARWPADRPTLDIGHLSITELTDEPAGLLMDPTATGQGIEITPDPILSFRREAYAVSHERRMQGI
>NZ_CP045802.1|WP_028597858.1|1302978_1304565_-|peptidase-M4-family-protein
MKRSVSALLGSILLLSSVSLVNAAPSMSVIPEDSLAPQFIGGDTNAAAAGGTSEDKVWAFLRSQQTKLGLTTSDLKTAFQIKDKQLDAGSGIEHFRLQQVVNGVPVYGADQTIHVDNKTGKVTSFLGAVIPSKKQEQFAAKALQPQLSPTDAIAVATAEAASRIGSLGASEKAPSAQLFVYAENGANNLVYETEVNVLEPEALRTRYLIDAVDGHIVLQYDLLQHATGTGTGVAGDTKTFQTTLSGSTYQLKDTTRGNGISTYTASNRTSLPGTLLTDSDNVWSDRAAVDAHAYAGQVYDFFKNKFGRNSLDGNGFAIRSTVHYSSRYNNAFWNGSQIVFGDGDGTTFTYLSGDLDVIGHELSHGVIEYTSNLRYLNESGALNESYADVLGNSIQAKNWLIGDDIYTPGVAGDALRSMSNPTLYGQPDHYANRYTGTADNGGVHTNSGITNKAFYLLAQGGTHNGVTVAGIGRDAAVNIFYNTVAYYLTSTSTFASAKNASIQAAKDLYGTSSPYVTSVTNAFRAVGL
>NZ_CP045802.1|WP_153782998.1|1304985_1305708_+|methyltransferase-domain-containing-protein
MGAEEIRSKEDVLAMLDALLQERSSFSWDRFYSDRERKVPFFIDLPDESLVQAVESGWIKPGKVLELGCGPGRNALYLAENGFDVHAVDLSEEAIAWAKQRALERGVQVRFERLNLLELSEQGRDCDLVYDSGCFHHIAPHRRMDYCRIVDEALRPGGCFALTCFKENGALGGSARSDWEVYRQMSLGGGIGFTASKLGRHFPDYERIECREMKDCGPESGCFGSSELLAAWFRKPQGSG
>NZ_CP045802.1|WP_153782999.1|1305825_1308540_-|aconitate-hydratase-AcnA
MPLQNQYSVRSTLEVGGKSYTYYRLEGLEEKGHGFISKLPVSIKVLLEGAIRQFDGRGITADHVSQLMNWAQKREDKEIPFIPARIVLQDLTGVPVVVDLAAMRETVKKNGGDPKKINPLVPVDLVIDHSVMVDAFGSPDALEINQRIEFERNAERYKFFRWAQTAFDNFRAVPPDTGIVHQVNLEYLASVAATKVIDGETVVFPDSLVGTDSHTTMINGLGVVGWGVGGIEAEAGMLGQPLYFVAPEVIGFKLTGMLAEGATATDLALTVTEILRKRGVVGKFVEFFGPGLSNISLPDRATVANMAPEYGATVGFFPVDAITLNFLRQTGRTEEQIELVEAYYKAQGMFRTDDTPDPTFTDVIELDLSTIVPSLAGPKRPQDRIELTAMKEAWNSTVRTPVDKGGYGLSDAKIEEVVEIKHANGKVSKMGTGAVVLAAITSCTNTSNPSVMLGAGLVAKKAVEKGLVKPEYVKSSLTPGSLVVTDYLVKAGLLPYLEQLGFHVAGYGCATCIGNSGPLPEDVSQAIADNDMTVAAVLSGNRNFEGRIHAQIKANYLASPPLVVAYALAGTVNIDFANEPIGHDQQGEPVYLRDIWPSSEEIANAASSAITPQMFRDKYDNVYTHNERWNQIPVPEGELYEWDENSTYIANPPFFENLADGIRDVADIKHAKTLLLMGDSVTTDHISPAGSIRADYPGGKYLLEHGVEKKDFNSYGSRRGHHEVMVRGTFANIRIRNQVAPGTEGSFTTYLPTDEVTSVYEASMKYQADKTNLIVIGGKEYGTGSSRDWAAKGTFLLGVKAVITESFERIHRANLVGMGVLPLCFQEGQGWKTLGITGRETFDIEGLTNDVKPGDQVTVTATREDGSSFQFQVTVRLDSLVEVDYYRNGGILQTVLRQMLSEQK
>NZ_CP045802.1|WP_153784676.1|1308972_1310112_+|AI-2E-family-transporter
MNNKFVLFLLVLLLVSVNVYVLAHITFIFAPLIVLVKTVLLPLLLAGVAYYLLNPLVDWMEKRGMKRGWIIAALYVIILGLLTLLVTIVVPVVREQIQGLIDNVPAYTKYVQDTFARYLGNDTVTELQREFNFDPQQLAREVSQRAGSIVQTTLTNIGGFLGTVTEFVLALVTLPFILFYMLRDGRRLPEFILKLLPTGLRPETRRVLSESNDQISSYIRGQIIVSICIGCLLYVGYLVIGLEYSLILAIVAACTAVVPYIGPAIAITPALVVAAFTSPIMLLKMIAVWTIVQLIEGKFISPQVMGKSLKIHPITIIFVILTSGKLFGFLGIILAVPGYAVLKVFVTHLFRWFMVNSKLYGPEPEYKILGVKRDSDLLP

Crispr_ID: NZ_CP045802_10

• CRISPR_ID: NZ_CP045802_10
• CRISPR_location: 1431233-1431306
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_10

Consensus_repeat	Method
GTTAAGTCGATTTTATCGAGCTA	CRISPRCasFinder

spacers of NZ_CP045802_10

>10.1|1431256|28|NZ_CP045802|CRISPRCasFinder
ATGCAGCCGCACGCCCGATTCGGAGCGG

CRISPR arrays and Neighbor proteins around NZ_CP045802_10

CRISPR arrays

The CRISPR arrays of NZ_CP045802_10

>merge|NZ_CP045802|10|1431233-1431306|CRISPRCasFinder
GTTAAGTCGATTTTATCGAGCTAATGCAGCCGCACGCCCGATTCGGAGCGGGTTAAGTCGATTTTATCGAGTTA

>NZ_CP045802|10|8|1431233-1431306|CRISPRCasFinder
GTTAAGTCGATTTTATCGAGCTA	ATGCAGCCGCACGCCCGATTCGGAGCGG
GTTAAGTCGATTTTATCGAGTTA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_153783052.1|1413263_1413668_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_052333576.1|1445398_1446232_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|223521
NZ_CP045802.1|WP_153783059.1|1436774_1439117_+|exosporium-leader-peptide	unknown	unknown	gnl|CDD|371823
NZ_CP045802.1|WP_153784683.1|1432882_1434064_-|Ger(x)C-family-spore-germination-protein	unknown	unknown	gnl|CDD|274338
NZ_CP045802.1|WP_153783060.1|1440200_1441904_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153783062.1|1443589_1444540_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223674
NZ_CP045802.1|WP_153784680.1|1416089_1417121_-|arabinogalactan-endo-1,4-beta-galactosidase	unknown	unknown	gnl|CDD|311610
NZ_CP045802.1|WP_052333595.1|1439394_1440204_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224054
NZ_CP045802.1|WP_153784681.1|1419415_1420978_+|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_CP045802.1|WP_153783061.1|1442013_1443588_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|173855
NZ_CP045802.1|WP_153783056.1|1425717_1426650_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223472
NZ_CP045802.1|WP_153784682.1|1426689_1428264_+|DUF3502-domain-containing-protein	unknown	unknown	gnl|CDD|270298
NZ_CP045802.1|WP_153783058.1|1434091_1435630_-|spore-germination-protein	unknown	unknown	gnl|CDD|377020
NZ_CP045802.1|WP_153783057.1|1431529_1432849_-|endospore-germination-permease	unknown	unknown	gnl|CDD|273333
NZ_CP045802.1|WP_153783055.1|1424778_1425699_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|226666
NZ_CP045802.1|WP_101808687.1|1428452_1430528_+|beta-galactosidase	unknown	unknown	gnl|CDD|224786
NZ_CP045802.1|WP_153783054.1|1421600_1422860_+|IS256-family-transposase	unknown	unknown	gnl|CDD|307151
NZ_CP045802.1|WP_153783053.1|1417568_1419407_+|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|225519
NZ_CP045802.1|WP_028597923.1|1414085_1415714_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|237894
NZ_CP045802.1|WP_084137557.1|1444536_1445487_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|131837

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_052333576.1|1445398_1446232_+|ABC-transporter-ATP-binding-protein	gnl|CDD|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	4.87484e-104
NZ_CP045802.1|WP_153783059.1|1436774_1439117_+|exosporium-leader-peptide	gnl|CDD|371823	pfam11962, Peptidase_G2, Peptidase_G2, IMC autoproteolytic cleavage domain. This domain is found at the very C-terminus of bacteriophage parallel beta-helical tailspike proteins. It carries the enzymic residues that induce autoproteolytic cleavage to bring about maturation of the folding process of the helix in a chaperone-like manner. The domain thus mediates the assembly of a large tailspike protein and then releases itself after maturation. These C-terminal regions that autoproteolytically release themselves after maturation are exchangeable between functionally unrelated N-terminal proteins and have been identified in a number of bacteriophage tailspike proteins.	4.67071e-27
NZ_CP045802.1|WP_153784683.1|1432882_1434064_-|Ger(x)C-family-spore-germination-protein	gnl|CDD|274338	TIGR02887, Spore_germination_protein_B3, germination protein, Ger(x)C family. Members of this protein family are restricted to endospore-forming members of the Firmicutes lineage of bacteria, including the genera Bacillus, Clostridium, Thermoanaerobacter, Carboxydothermus, etc. Members are nearly all predicted lipoproteins and belong to probable transport operons, some of which have been characterized as crucial to germination in response to alanine. Members typically have been gene symbols gerKC, gerAC, gerYC, etc. [Transport and binding proteins, Amino acids, peptides and amines, Cellular processes, Sporulation and germination].	1.5234e-91
NZ_CP045802.1|WP_153783062.1|1443589_1444540_+|ABC-transporter-permease-subunit	gnl|CDD|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.06662e-114
NZ_CP045802.1|WP_153784680.1|1416089_1417121_-|arabinogalactan-endo-1,4-beta-galactosidase	gnl|CDD|311610	pfam07745, Glyco_hydro_53, Glycosyl hydrolase family 53. This domain belongs to family 53 of the glycosyl hydrolase classification. These enzymes are enzymes are endo-1,4- beta-galactanases (EC:3.2.1.89). The structure of this domain is known and has a TIM barrel fold.	4.06004e-92
NZ_CP045802.1|WP_052333595.1|1439394_1440204_+|ABC-transporter-ATP-binding-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	4.04079e-82
NZ_CP045802.1|WP_153784681.1|1419415_1420978_+|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	7.0121e-49
NZ_CP045802.1|WP_153783061.1|1442013_1443588_+|ABC-transporter-substrate-binding-protein	gnl|CDD|173855	cd08490, PBP2_NikA_DppA_OppA_like_3, The substrate-binding component of an uncharacterized ABC-type nickel/dipeptide/oligopeptide-like import system contains the type 2 periplasmic binding fold. This CD represents the substrate-binding domain of an uncharacterized ATP-binding cassette (ABC) type nickel/dipeptide/oligopeptide-like transporter. The oligopeptide-binding protein OppA and the dipeptide-binding protein DppA show significant sequence similarity to NikA, the initial nickel receptor. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	7.564e-164
NZ_CP045802.1|WP_153783056.1|1425717_1426650_+|ABC-transporter-permease-subunit	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.58091e-63
NZ_CP045802.1|WP_153784682.1|1426689_1428264_+|DUF3502-domain-containing-protein	gnl|CDD|270298	cd13580, PBP2_AlgQ_like_1, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	2.75579e-30
NZ_CP045802.1|WP_153783058.1|1434091_1435630_-|spore-germination-protein	gnl|CDD|377020	pfam03323, GerA, Bacillus/Clostridium GerA spore germination protein.	0
NZ_CP045802.1|WP_153783057.1|1431529_1432849_-|endospore-germination-permease	gnl|CDD|273333	TIGR00912, Spore_germination_protein_A2, spore germination protein (amino acid permease). This model describes spore germination protein GerKB and paralogs from Bacillus subtilis, Clostridium tetani, and other known or predicted endospore-forming members of the Firmicutes (low-GC Gram positive bacteria). Members show some similarity to amino acid permeases. [Transport and binding proteins, Amino acids, peptides and amines].	1.62383e-45
NZ_CP045802.1|WP_153783055.1|1424778_1425699_+|ABC-transporter-permease-subunit	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	1.74771e-106
NZ_CP045802.1|WP_101808687.1|1428452_1430528_+|beta-galactosidase	gnl|CDD|224786	COG1874, LacA, Beta-galactosidase [Carbohydrate transport and metabolism].	0
NZ_CP045802.1|WP_153783054.1|1421600_1422860_+|IS256-family-transposase	gnl|CDD|307151	pfam00872, Transposase_mut, Transposase, Mutator family.	2.84833e-144
NZ_CP045802.1|WP_153783053.1|1417568_1419407_+|HAMP-domain-containing-protein	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	3.21141e-49
NZ_CP045802.1|WP_028597923.1|1414085_1415714_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|237894	PRK15064, PRK15064, ABC transporter ATP-binding protein; Provisional.	0
NZ_CP045802.1|WP_084137557.1|1444536_1445487_+|ABC-transporter-permease-subunit	gnl|CDD|131837	TIGR02790, Nickel_transport_system_permease_protein_nikC., nickel ABC transporter, permease subunit NikC. This family consists of the NikC family of nickel ABC transporter permeases. Operons that contain this protein also contain a homologous permease subunit NikB. Nickel is used in cells as part of urease or certain hydrogenases or superoxide dismutases. [Transport and binding proteins, Cations and iron carrying compounds].	5.61966e-102

Protein sequences

>NZ_CP045802.1|WP_101808687.1|1428452_1430528_+|beta-galactosidase
MAKKLKFPPVSPKLPVMMHGADYNPDQWQHDPAVLEEDIRLMKLAGCNVMSVGIFAWAALEPEEGRFEFGWMDRLLDTFAENGIYAWLATPSGARPAWMSEKYPEVLRVGANRVRNLHGMRHNHCYTSPAYREKTRLMNAKLAERYAHHPAVLGWHISNEYGGECHCGYCQDAFRAWLKERYGSLDALNAAWWATFWSHTYTSWEQVESPAPHGETMVHGHNLDWRRFVTHQTADFCRAEIAPLKAANPELPATTNLMDLFYDLDYRELAKVIDVVSWDAYPMWHSQASDAGTAAWFAFNHDLFRSLKQQPFLLMESTPSLTNWQPVSKLKRPGMHRLSSLQAVAHGSDSVQYFQWRKSRGSSEKFHGAVVDHVGHEHTRVFQDVAELGRELAGLTELVGTGVPAETAIVFDWDNRWAVNDAQGPRNGGLRYEQTVVQHYKALWEMGVPVDVIGSADPLDGYKLLILPMTYLLRQDAGERIEAFVRGGGTVAMTYWSGVVDEHDLCRLDGFPGPLRKAAGVWAEEIEGLHDGEENRLVLREGNPLGLSGSWRIHEICELIHAEGADVVGEYGEDFYAGRPALTVHAFGEGRVHYLAARVADEAFYGAWYGALVREAGVARALEAELPPGVTAQLRSDGEHDYVFVLNFSGAAAQVRLGESGLVRFESGEPAGAELALPAHGAALLKRAARR
>NZ_CP045802.1|WP_153784682.1|1426689_1428264_+|DUF3502-domain-containing-protein
MKTKKATLLPLAAALSLTAVLSACSGGGNAEPSAAPTASPAPSAAAGESSGAVDTSQEVKLKMILVGGKPVDYDKVFGELNAKLKEKINATVDVEFLDWSDWNQKYPLKFAANEDFDLVYTANWAYYNDQALKGGFLELTEDMLKKYAPQTMESMPAVSWDQAKVDGKLYMVPNNNVEVNDKVVLYREDLRKKHNLPEINSLDTYAQYLKAIAANEKGIIPYGAKAGDGWKWHEMDQATLEQHNDWNLVDTTLPLAYKMDDATGQIFNIYDTQEFKDLLVYYKDLADSGVWSKNVVSNKNDVWQDIKAGKVASYAAQNLGTAGSNLAEMRRDNPSLEVAIADITPDGKKIAAISTQNGMAVHATSKNPERSLMLIDLLQNDKEIHDLTMYGISGENYVPEGDDKYTAGPAAGNYTGFSNWGWNSPLNRKDASYPKEADDIFNSWQSKIYHFPLETFVFNGEKVKAEVANIGNVMTRYAIPLEYGLIKDIDKGHADLIKQLKAAGIDKVQAEMQAQVDAFLAAQK
>NZ_CP045802.1|WP_153783056.1|1425717_1426650_+|ABC-transporter-permease-subunit
MKNQAAIAAASDAVRSKAVRRDMLLFRIIGYAVLALLALFCFVPFLLVLSSSLTSESSIIENGFQLLPTEFSTEAYSLLFQYPEQILRAYGVTIGVTALGTFAGLFLTSMTAYVLSRKDFRWRNSFSFFFFFTTLFSGGLVPWYLLIVNYLQLKDTFIVLVLPMLLNVFYIIVMKSFMSGIPEAIVESAKMDGADDFRIYWQLILPLAKPALATIGLFLALGYWNDWYNALLFVSNDNLMPLQYYLYKMLGNMDGMRKALISSGAVVNLSIPTESLKMAMTVTAIGPILLAYPFIQRYFVQGLTIGSVKG
>NZ_CP045802.1|WP_153783055.1|1424778_1425699_+|ABC-transporter-permease-subunit
MNRGGFWSDVSKYRVLLLMLLPAVLFFLLFAYIPMAGIVLAFKQFNYNGGIFGSPWNGLDNFRFFFESGDAWRVTRNTALYNIAFIIVNNVLQIAAAILLFEAARPFFRKIFQTMLFLPYFISWVVVGAIAYNLFNYDYGMLNSVLGWLGMEPIDVYNTAAYWPLLLVLISAWKALGYGTVMYLAAITGLDREMYEAAEIDGANIFQRIIHITIPNLMPTLIILVLLAIGNIFRGDFGMFYNMVGNNGILFSTTDVIDTYVFRALTANNDIGMSAAAGFYQSILGFVTILVANWAVRRYDKDRALF
>NZ_CP045802.1|WP_153783054.1|1421600_1422860_+|IS256-family-transposase
MTQYQITVDQDILHQLFIGTDRDAGVARLLETVLNQVLTAQATDQLAAQTYERTSERKGYRNGSYERDVITRAGSVTLRVLRFRDGSFSTELFARYQRSEQALVLSLMEMVINGVSTRKVTKITEELCGTEFSKSTVSHLCKQLDPAVHDWNNRSLADHAFPFITIDAIYVKVREEGRICSRGVLVGYGVNEQGRREILGLRVDDTESEESWGAYFRWLKERCLHGVELVTSDYHGGLVKAIEKEFQGVSWQRCQTHFIKNVLNAAPKALQSEIKSRVRSIFDAPDMKTARSYLEQTLEAYAETAPKAMKILEDGFEDAVAVLAFPEAYRVRLRTSNGMERLNGEIRRRETVIRIFPNRASVLRLIGAMLMEENEYWMTKKPYMDMTDFKAWKKQKATQGAGSEEQETSTTMTEATDSL
>NZ_CP045802.1|WP_153784681.1|1419415_1420978_+|response-regulator
MPIRVLLVDDEAVDLEWLRRRVAGSGLPVQVAGTASSGFAALDLLQREQVDVILTDIRMPIMSGIEFARRAKEARPHVKIVFISGHEDFHYAKEALRLSASGYLLKPVDDEELLAMLGTLCRDVEQEKRASRSVSEALSLAARELLLRWLGGDRSPLLEEHLQPYLLPAAEHGASCALIEIDDLEWKAASLGEAERDRHIAAMGAFLHDFAERRQLGLMLAGLPGARAVLIARAGADPRLEELVAELARRFPLTVTIGVGRPAGRWQELPESYREAQAALSAKWLLGKNRVLRESPEPLGDEGPSAAQEAVIDRMLAAILQYDLVEIDDCLLELFGGSGRLRRSEAYPLVLRLTSKLHADLQAMDENLYELLKWDTHEPGVMFQFETMNDLLSWLRKRLFELSELLLIKSRRHSRKLIDEIKAYVEERLEQKVTLKETAAQFSFTPNYLGHLFKEETGQHFSDYLLERKLKLTCALLEEPTLKIYEIADRMGYKNIVYFNRQFKQATGMSPGEYRKKAGI
>NZ_CP045802.1|WP_153783053.1|1417568_1419407_+|HAMP-domain-containing-protein
MSGAKRKSYIPYSYKMMIPYLLLVLVTDALIGTISYRMLVESRTEIARTNIQAAMQQTRTNMHYQMEEIKRISDTLFGSVPFQRALQKRGDELQAYLTMLDEIVPKLQEPLQLFGNPLRIELYTTNPDLYEIEGDDPSTKIERSDYYVLSADRLRGSAWAEQAGAGDGSRWMQVESDAEHRQLSHLTRLLSYSDYQTAIGYIRITARLDDLLGRFDAFPVEKGMTLRLLDQPSGRTLYEKGDAHEADAPGHLTLSEAVPGSGYVIQAVVSQRYLQEDARRLGLVIVGVCSVSFAVMALIGFMVARLSGRKMRKIVTLVQSFQDGSLEKRIRFSGKDEFVQIADAFNTMAEHVKELISSVFAQGQKRKQAELEALQAQINPHFLYNTLSTISSLANMGETRQVTEMVKGLSRFYRLSLNEGRVLIPLGQELEQVQTYLDIQRVKYADAFTVHLDAEPDIGELRVMKLILQPFVENVFKHAWYGESIAIRITARRLGADLELKVIDNGVGMNAEALERLRSGTAGSAAAPAASGLAGEPSEFAPAAAVRASGSAGAGGSYGIRNVDERIRLRYGERYGIEVGSVFGGGTTVRILLPAEGEWEDGIVREEKEEGR
>NZ_CP045802.1|WP_153784680.1|1416089_1417121_-|arabinogalactan-endo-1,4-beta-galactosidase
MAALLLLLAPAWEGAGGAGVGGKAAAAPAFAKGADISWVAAMEAQGYKWKDKNGVTRDIFNILKNDYGLNSARIRVWVNPNMSDYGNGYLNADKAAALAARAKAQGMSVMLSLHYSDSWADPGKQTKPYAWTGFTFNQLMDAVWSHTVYVMNTMKAKGVTPDWVQIGNETNDGMLWQDGRASVNMKNYAWLVNTGNNAVKSIFPSTKTIVHLANGYDNALFVWNIGGLIANGATFDYIGMSLYPSVSDWQTKVTQTVANANDMIARYGKSVMICEIGLDYNQPAASKSFIADIKTKIRNISGGKGLGVFYWEPQSTPGYNGGYNKGAWQADGKPTIALDGFLN
>NZ_CP045802.1|WP_028597923.1|1414085_1415714_+|ATP-binding-cassette-domain-containing-protein
MISTSGISLRYGKRALFEDVNIKFTPGNCYGLIGANGAGKSTFLKILSGEIEPNTGEVHITPGERMAVLKQNHFEYDEVPVLMTVIMGHKKLYDVMNEKNALYAKSDFTDEDGMRAGELEAEFADMNGWEAESEAAEMLNGLGITPDLHDKLMKELDGNAKIRVLLAQALFGTPNILLLDEPTNHLDMQSIEWLEKFLSTYEGTVVVVSHDRHFLNQVCTHIADIDFGKVQMYVGNYDFWYESSQLALALQRDANKKKEDKVKELQAFIQRFSANKSKSKQATSRKKMLDKITLDDIRPSSRKYPFINFKGEREAGKQILLIEGISKNVDGEQLLSNFTLTVNKGDKIAFVGPNTLPKTALFQIITGESEADAGTYQWGITTIQGYFPKDNSKYFDGVEMNLVDWLRQYSKDQDESFIRGFLGRMLFSGDEALKKASVLSGGEKVRCMLSKIMLSGANVLVMDEPTNHLDLESITALNNGLIDTDCTVLFTSHDHQFVQTIANRIIEITPGGVIDRLMTYEEYLESDDVKAMRDRLYAGQPS
>NZ_CP045802.1|WP_153783052.1|1413263_1413668_+|hypothetical-protein
MISEIEEFVANERASAKGQRLEMLERDLHGTLKLLEKAILPVFNSLDGFSLEFEFKSSYGYNYYADVYYKPLHAIFECDGFVPHAELMTRERFAWERQRSRAISLGGYRYLPFSYDELDKKKRSLPSSDLRASW
>NZ_CP045802.1|WP_153783057.1|1431529_1432849_-|endospore-germination-permease
MLLACSRRGPGPARAAAARPQKGARPGRGHRPRRTAAFRGARPARSASQSARSDKPVPRGEDRMKPIGNGRISARQFKIMIVFSLIGDSILILPNLMGNISHQDAWLSQLAAIACGMALAWAYAALLGRLGRLSFVGAWTALLGRIAGSALGLVYAYGFYAMVLALLAEISLFMRAQMMRETPAEAIMLAFLIVIAAGLRYGIETFARTSELLYPIFIAMFLFLSLCLLPQIKADQLLPIAGAGMPQIAEGSFLSFAYGFLESAVLLMLTPYLEDDRKAARSAIFNGFLTGGLMLFLILLLCVLVLGPSMMELKHYPTFQLAQRIEIGRFLERLEALLTFLWIVTVFYKALLYSFSLQKTISEIAQLQDDRILAMPLCLLMLAGGMISVPNIAAYNELIKAQFPYYDLILYLGGPLLLLLLLAFPAARRRLEARQPRAG
>NZ_CP045802.1|WP_153784683.1|1432882_1434064_-|Ger(x)C-family-spore-germination-protein
MRICLVLSCLLLLSGCWSRRELNDLLVVLGMGIDWVDGQYLVSFQVVNPSEISSKTKGASRAPGTLYQGRGNTIFEAARSLTTQAPRLMYLGHLQLFVLSEEIARRGVASVIDSPLRDNEARMDYNVVIARGATAAEILDLYTPLERLPTYSMQQSLRTSERSWAPTVAVTMSDMINKLSDDGQQLVLTGIEIEGSRKQAGRPSNLTGFRPAASYNYRGIGAFKGDKLIGWLNEKESKGFTDLTDNLDSTSIELPCSPTGYTGIEVTSSVTRLMPRLRDGKPEFLVKIWAQGDVVENACSMVDFNRDATFVDLEKRSENIVRSNAEAAIRWAKRHETDVLGFGSALAKKHPAYWERARDDWNSSGFSQAAIVFDIDVVIRKTGTIGNSVKPKE
>NZ_CP045802.1|WP_153783058.1|1434091_1435630_-|spore-germination-protein
MKPTFSWEGTEPGMLQPLPLDPDAGRLLETIRQDMGGSGDLVIRRFGDPAAPSPPAALVYIDGISDEETADRYISDVLQAAGAEEDGLAPPAAAVASAALRLLGTIGSGDPVPDMAALYERLLSGSAILVLDGSELAFAASNAKWKSREIAESPNQTAIRGPRESFTETMRVNTALLRRKIKDPRLWMESMQLGRMTKTEVCLIYIQGLAKPSVVEEARSRLQAIDIDGVLDSGYVEELIADDRRSFFPTIKNTELPDSVAGELMEGKIAILVDGSPDALIAPAPFFTFMQSAEDYYQAALYSSLLRMLRLLGLFIALLLPSIYIAITTFHRDMLPFTLLFSLMAQREGVPFPAFVEALVMEITFEILREAGLRMPRPIGQAVSVVGTLVIGQAAVDAGIVSAAMVIVVSVTAIATFTLPSYSISIPIRMLRFAFMAVAASFGLYGIILALLLLLHLSSLKTFGESYMSPIAPLRTRGLADTLARAPRWTGFLQPMLSRRAGARRYRDRRHD
>NZ_CP045802.1|WP_153783059.1|1436774_1439117_+|exosporium-leader-peptide
MDGQCNRQAIGPCSDAGGADTTASGPAAHAEGSETVASGSAAHAEGYRTNAAGDSSHAEGSTTVAAGSASHAEGFTTEALSDAAHAEGSYATASGEASHAEGSRTLAAGDVSHAEGSGTEALGTAAHAEGYQTTAAADSSHAEGSGTTASGSASHAEGYRTAASLDAAHAEGSGTTASGPAAHAEGESSSAEGESSHAEGTGTRSIGAASHAEGSGTRAAGDQAHSEGLGTEASGLASHAEGRSTDAFGPYAHAEGASTEASGESSHAEGAATLASGTTAHAEGSNTVASGNFSHAEGYQTTASGTYAHAEGSLTAATAFNSHAEGYETQASGYAAHAEGNATIASGNDSHAEGATTTASAFAAHAEGNTTVASGGNSHAEGNATLAQGTNSHAEGSTGRALGINSHAEGFNGEASGDNSHAEGADTIASGTSAHSEGSLTTASGNFSHAEGYQTQALDNYAHAEGSLTVASAFNTHAEGYQTTASGYASHAEGSGSSATASYAHAEGLTTEASGYGSHAEGVSTVASGSRAHAEGGNTTASGNYTHAEGLQTTADQAGSHIMGRYGTTLYPYSWHVANGTSAANPGLAAVLQGSTGNMYIDGSYFSGGADYAELYETVDGAPLEPGYFVTLEGEQIRPAEAADGYVLGVTSAVPTLVGDAAELRSPDAYLRDEWGRIVLETVTIPAELAPDGTVIAPAYAVEQPVVDPAYDPTVPFVPRRLLPGWAPVGLIGKLLVRDDGSCAPNGYCLPGSGGVATTAANGYRVLSRTGPNQIRIQMK
>NZ_CP045802.1|WP_052333595.1|1439394_1440204_+|ABC-transporter-ATP-binding-protein
MRVRNLRKWYGSKQVLKGIDLEAYPGQIIGYIGPNGAGKSTTQKLLLGLEQGYDGYIEVLGQDISYGSYEYKSRIGYVPETAEIYDMLTAREYLAFSGQLYGLPREAAERKGERLLALFGLEEMVDRRIDSFSKGMRQKVMLSAAVLHDPDVIFLDEPLSGLDAGSVAVVKEILTRLAARGKAIFYSSHIMDVVEKISSRIVLLHDGQVAADGSFAELQARSEEGSLERIFNRMTGFDEQEAIAEQFCSTIAMTPEQLAAEASEETKRP
>NZ_CP045802.1|WP_153783060.1|1440200_1441904_+|hypothetical-protein
MKEFLSIRLLDRFRGAFTRAGYDFPALRVILQAKLTMGRRRPTGLMNAFGGTRRTEGDELQNSFFSSLWIYVGISLFLVPMAVFLEQPILRMGMLSAVQMLLLSSLLLSDFSTTLLDTRDRTILGVRPVSPKTAGMARLLHAVVYLGWTVSALTALPLLAVLLAHGPASAAVYAVHAALQAALLMSLTAAVYYGVLRLWDGERLKDMINYVQIFLAAVVLGGSQLAVRLFNFSLAEQALQAQWWWTLVPPLWFAAPHGLIDGQGGGWLIACTVLSVAAPLLGLLLYLRLLPSFERSLHKLASKDAPDRPRQRRRRMPMASRLGRLLLRDPRERALLDFSLASLSRERDFKLKVYPSLGYAVLIPVLFVLPTLSGNEFRTDELSPNWSLALYGTGLAVPMLLLMLRFSSRPLAAWIFHAAPGLREGQVHRAAAAAVLLRLGLPALAVPTLLFLAFFGTAILPHLAGLIPALSIFAVIGYRVIPRRLPFAEPFPTGNNVGGAGYTFLLMFLLLGLSLLHVLIANLAGPVGLWLYAVLLLAGQHFSWKYGFREGAAVKKAPANGNPTFRA
>NZ_CP045802.1|WP_153783061.1|1442013_1443588_+|ABC-transporter-substrate-binding-protein
MALTAWKKWKKYALATAISASMIVSAGCSGGASEPNAGDQDRTAAEAAASKRAVVLFHVKSSTLDPADNIITVKAGIAETLTRLDADLGVKPWLAASWTAVDASRWEFLIRDNVTFQDGSPLTAEAVKASLERTMARNESMKLALKIRSMTADGQKLAVETLEPHPALASELLNPHTAIIQVKEEASIASAPVGTGPFRVASFAQDARIELERHDGYWDGAAKLEQVSFRFNEDGNVRALALQSGEADIATQLPAESVEAIRLNPKLKVESEPGLRVHFLLFNPQGEATGDLRVRQAFDVLLDRRSIVEDIMLGHAAPANGPFNDRLPFGRAAAAAEQDLDKAKQLLEQAGYAPDAGGSLVKDGKKLTLKLLTYKARPELPLIAQLLQSDAAKIGIAIDIRTVENIDDTIRQNRDWDLVTYSNLSAPRGDGGFFLNSALMPGGSLNAADIRIDELTDVMKTLNATSEAERRIALTREAVDIAMSRTPHAYAVYPNLIVGLNERIAGWRTDPSEYTILTNELDVS
>NZ_CP045802.1|WP_153783062.1|1443589_1444540_+|ABC-transporter-permease-subunit
MLALVRARLLQLLLVLFFMSILIFGLMKLAPGDPVFALLKADEVKTTMADEQALRESLGLDKPMLVQYGQWLARVARLDFGDSLMRQRPVLELYVEKLPATVELALGGMAFMLALAVPAGLLAARFPGRLPDHAGRAFSLLGASIPVFWIGLLLIYLFAYRLQWLPFMGRGEDWRQLILPSVTLGFGLSAVHASLLRSGMLASLSQPYIRAARARGIRESTIYGKYALRGAIAPVLTVFGMTLGSLLAGSVVVETLFSWPGIGLMAVEAIFQRDYPLVQGFLFLSGALIVLVNLAVDLLYGWIDPRVRLSGKGGRR
>NZ_CP045802.1|WP_084137557.1|1444536_1445487_+|ABC-transporter-permease-subunit
MKAVISIGAAALRRLASRPWGIAGLAVGAVLAVLAFFGSALAPHDPLTVRMDLRLLPSSWTYPLGTDALGRCLLSRLLVGAQTTLGLAGLVIVAVLLIGVPLGLLAGYAGGRVDAFLMRIVDGLSTLPDFLLVIAISGFLGPSQVHLIVAIVAINWIGYARIVRGVVLSEREKDYVAAAIVSGCKPAALLRRHLLPSVLSPVLVYAALDIGKTILVVSSLSFLGLGAQPPSPEWGAMLNDGRAYFQTAPQLMVYPGLAIMLVVIAFNLMGEGLRSRLDQRYSERRSFDDGSSGSNRLAGRTMHRRRTGKPREGNRS
>NZ_CP045802.1|WP_052333576.1|1445398_1446232_+|ABC-transporter-ATP-binding-protein
MTEAAAPIVSLAGLCIGDGRENLVKGIDLEIAPGERLALVGESGSGKSLTASAILGLLPAPLRVTAGTVRFQGTDLAGLSRKERRKGLGARIGCVFQDYRGSFSPYHTVGSQLAEALRTARPMKRKEAKQMALDSLEQVGLPAERAYASYSFQLSGGQLQRAALACVLLLRPELLIADEPTTALDIVSGRSVMQLMLDIQRQTGCGILLISHDLNLVLDWADRAAVMRKGRLVEEGPCDVLRTSASHPYTQELLAACPSLDDALHRHEGGHVHEAHC

Crispr_ID: NZ_CP045802_11

• CRISPR_ID: NZ_CP045802_11
• CRISPR_location: 1554844-1554948
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_11

Consensus_repeat	Method
TGCAAGCGGCAGGGGCGGAAGGAGCGGC	CRISPRCasFinder

spacers of NZ_CP045802_11

>11.1|1554872|49|NZ_CP045802|CRISPRCasFinder
AACGGTGATTAAGTCGGTGTAAGCTACAGGGGCGGGGCGATCCAGTCGG

CRISPR arrays and Neighbor proteins around NZ_CP045802_11

CRISPR arrays

The CRISPR arrays of NZ_CP045802_11

>merge|NZ_CP045802|11|1554844-1554948|CRISPRCasFinder
TGCAAGCGGCAGGGGCGGAAGGAGCGGCAACGGTGATTAAGTCGGTGTAAGCTACAGGGGCGGGGCGATCCAGTCGGTGCAGGCGGCAGGGGCGGAAGGAGCGGC

>NZ_CP045802|11|9|1554844-1554948|CRISPRCasFinder
TGCAAGCGGCAGGGGCGGAAGGAGCGGC	AACGGTGATTAAGTCGGTGTAAGCTACAGGGGCGGGGCGATCCAGTCGG
TGCAGGCGGCAGGGGCGGAAGGAGCGGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_028600625.1|1546169_1546448_+|PqqD-family-protein	unknown	unknown	gnl|CDD|377508
NZ_CP045802.1|WP_153783111.1|1545288_1546173_+|hypothetical-protein	unknown	unknown	gnl|CDD|275080
NZ_CP045802.1|WP_153783116.1|1562687_1563653_-|Ku-protein	unknown	unknown	gnl|CDD|238408
NZ_CP045802.1|WP_028600603.1|1564271_1564469_+|H-type-small-acid-soluble-spore-protein	unknown	unknown	gnl|CDD|377962
NZ_CP045802.1|WP_028600463.1|1544777_1544993_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028600608.1|1556735_1557209_+|polymer-forming-cytoskeletal-protein	unknown	unknown	gnl|CDD|377376
NZ_CP045802.1|WP_101808742.1|1564515_1564716_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153783112.1|1552010_1552268_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_052333635.1|1563951_1564218_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153783115.1|1561244_1562687_-|hypothetical-protein	unknown	unknown	gnl|CDD|185715
NZ_CP045802.1|WP_084137587.1|1550831_1551338_+|DUF1854-domain-containing-protein	unknown	unknown	gnl|CDD|378095
NZ_CP045802.1|WP_101808730.1|1546440_1547253_+|hypothetical-protein	unknown	unknown	gnl|CDD|131283
NZ_CP045802.1|WP_043112008.1|1552573_1553536_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224054
NZ_CP045802.1|WP_146000514.1|1557539_1558244_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_127464560.1|1551676_1551910_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153783113.1|1553528_1554344_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|378937
NZ_CP045802.1|WP_028600606.1|1560326_1561223_-|DNA-polymerase	unknown	unknown	gnl|CDD|240131
NZ_CP045802.1|WP_101809435.1|1548720_1550835_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|224055
NZ_CP045802.1|WP_101808743.1|1564992_1565868_+|YitT-family-protein	unknown	unknown	gnl|CDD|224203
NZ_CP045802.1|WP_153783114.1|1555091_1556519_-|cardiolipin-synthase	unknown	unknown	gnl|CDD|234967

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_028600625.1|1546169_1546448_+|PqqD-family-protein	gnl|CDD|377508	pfam05402, PqqD, Coenzyme PQQ synthesis protein D (PqqD). This family contains several bacterial coenzyme PQQ synthesis protein D (PqqD) sequences. This protein is required for coenzyme pyrrolo-quinoline-quinone (PQQ) biosynthesis.	6.22874e-15
NZ_CP045802.1|WP_153783111.1|1545288_1546173_+|hypothetical-protein	gnl|CDD|275080	TIGR04249, SCM_chp_ScmC, SynChlorMet cassette protein ScmC. A biosynthesis cassette found in Syntrophobacter fumaroxidans MPOB, Chlorobium limicola DSM 245, Methanocella paludicola SANAE, and delta proteobacterium NaphS2 contains two PqqE-like radical SAM/SPASM domain proteins, a PqqD homolog, and a conserved hypothetical protein. These components suggest modification of a ribosomally produced peptide precursor, but the precursor has not been identified. Members of this family are designated ScmC.	7.01891e-13
NZ_CP045802.1|WP_153783116.1|1562687_1563653_-|Ku-protein	gnl|CDD|238408	cd00789, KU_like, Ku-core domain, Ku-like subfamily; composed of prokaryotic homologs of the eukaryotic DNA binding protein Ku. The alignment includes the core domain shared by the prokaryotic YkoV-like proteins and the eukaryotic Ku70 and Ku80. The prokaryotic Ku homologs are predicted to form homodimers. It is proposed that the Ku homologs are functionally associated with ATP-dependent DNA ligase and the eukaryotic-type primase, probably as components of a double-strand break repair system.	1.66562e-121
NZ_CP045802.1|WP_028600603.1|1564271_1564469_+|H-type-small-acid-soluble-spore-protein	gnl|CDD|377962	pfam08141, SspH, Small acid-soluble spore protein H family. This family consists of the small acid-soluble spore proteins (SASP) of the H type (sspH). SspH are unique to spores of Bacillus subtilis and are expressed only in the forespore compartment during sporulation of this organism. The sspH genes are monocistronic and are recognized by the forespore-specific sigma factor for RNA polymerase - sigma-G. The specific role of this protein is unclear but is thought to play a role in sporulation under conditions different from that of the common laboratory tests of spore properties.	4.09906e-19
NZ_CP045802.1|WP_043112008.1|1552573_1553536_+|ABC-transporter-ATP-binding-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	1.30213e-90
NZ_CP045802.1|WP_028600608.1|1556735_1557209_+|polymer-forming-cytoskeletal-protein	gnl|CDD|377376	pfam04519, Bactofilin, Polymer-forming cytoskeletal. This is a family of bactofilins, a functionally diverse class of cytoskeletal, polymer-forming, proteins that is widely conserved among bacteria. In the example species C. crescentus, two bactofilins assemble into a membrane-associated laminar structure that shows cell-cycle-dependent polar localization and acts as a platform for the recruitment of a cell wall biosynthetic enzyme involved in polar morphogenesis. Bactofilins display distinct subcellular distributions and dynamics in different bacterial species, suggesting that they are versatile structural elements that have adopted a range of different cellular functions.	1.01613e-28
NZ_CP045802.1|WP_028600606.1|1560326_1561223_-|DNA-polymerase	gnl|CDD|240131	cd04861, LigD_Pol_like, LigD_Pol_like: Polymerase (Pol) domain of bacterial LigD proteins similar to Pseudomonas aeruginosa (Pae) LigD. The LigD Pol domain belongs to the archaeal/eukaryal primase (AEP) superfamily. In prokaryotes, LigD along with Ku is required for non-homologous end joining (NHEJ)-mediated repair of DNA double-strand breaks (DSB). NHEJ-mediated DNA DSB repair is error-prone. PaeLigD is monomeric, containing an N-terminal phosphoesterase module, a central polymerase (Pol) domain, and a C-terminal ATP-dependent ligase domain. Mycobacterium tuberculosis (Mt)LigD, also found in this group, is monomeric and contains the same modules but these are arranged differently: an N-terminal Pol domain, a central phosphoesterase module, and a C-terminal ligase domain. It has been suggested that LigD Pol contributes to NHEJ-mediated DNA DSB repair in vivo, by filling in short 5'-overhangs with ribonucleotides; the filled in termini would then be sealed by the associated LigD ligase domain, resulting in short stretches of RNA incorporated into the genomic DNA. The PaeLigD Pol domain in vitro, in a manganese-dependent fashion, catalyzes templated extensions of 5'-overhang duplex DNA, and nontemplated single-nucleotide additions to blunt-end duplex DNA; it preferentially adds single ribonucleotides at blunt DNA ends. PaeLigD Pol adds a correctly paired rNTP to the DNA primer termini more rapidly than it does a correctly paired dNTP; it has higher infidelity as an RNA polymerase than it does as a DNA polymerase, which is in keeping with the mutagenic property of NHEJ-mediated DNA DSB repair. The MtLigD Pol domain similarly is stimulated by manganese, is error-prone, and prefers adding rNTPs to dNTPs in vitro. The MtLigD Pol domain has been shown to prefer DNA gapped substrates containing a 5'-phosphate group at the gap.	4.77096e-87
NZ_CP045802.1|WP_153783115.1|1561244_1562687_-|hypothetical-protein	gnl|CDD|185715	cd07906, Adenylation_DNA_ligase_LigD_LigC, Adenylation domain of Mycobacterium tuberculosis LigD and LigC-like ATP-dependent DNA ligases. Bacterial DNA ligases are divided into two broad classes: NAD-dependent and ATP-dependent. All bacterial species have a NAD-dependent DNA ligase (LigA). Some bacterial genomes contain multiple genes for DNA ligases that are predicted to use ATP as their cofactor, including Mycobacterium tuberculosis LigB, LigC, and LigD. This group is composed of ATP-dependent DNA ligases similar to Mycobacterium tuberculosis LigC. ATP-dependent polynucleotide ligases catalyze phosphodiester bond formation using nicked nucleic acid substrates with the high energy nucleotide of ATP as a cofactor in a three step reaction mechanism. DNA ligases play a vital role in the diverse processes of DNA replication, recombination and repair. Members of this group contain adenylation and C-terminal oligonucleotide/oligosaccharide binding (OB)-fold domains, comprising a catalytic core unit that is common to all members of the ATP-dependent DNA ligase family. The adenylation domain binds ATP and contains many of the active-site residues. The common catalytic core unit comprises six conserved sequence motifs (I, III, IIIa, IV, V and VI) that define this family of related nucleotidyltransferases. LigD consists of a central ATP-dependent DNA ligase catalytic core unit fused to a C-terminal polymerase domain and an N-terminal 3'-phosphoesterase (PE) module. LigD catalyzes the end-healing and end-sealing steps during non-homologous end joining.	3.79959e-28
NZ_CP045802.1|WP_084137587.1|1550831_1551338_+|DUF1854-domain-containing-protein	gnl|CDD|378095	pfam08909, DUF1854, Domain of unknown function (DUF1854). This potential domain is functionally uncharacterized. It is found at the C-terminus of a number of ATP transporter proteins suggesting this domain may be involved in ligand binding.	3.21337e-35
NZ_CP045802.1|WP_101808730.1|1546440_1547253_+|hypothetical-protein	gnl|CDD|131283	TIGR02228, Signal_peptidase_I_W, signal peptidase I, archaeal type. This model represents signal peptidase I from most archaea, a subunit of the eukaryotic endoplasmic reticulum signal peptidase I complex, and an apparent signal peptidase I from a small number of bacteria. It is related to but does not overlap in hits with TIGR02227, the bacterial and mitochondrial signal peptidase I.	2.49089e-08
NZ_CP045802.1|WP_101809435.1|1548720_1550835_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	0
NZ_CP045802.1|WP_153783113.1|1553528_1554344_+|ABC-transporter-permease-subunit	gnl|CDD|378937	pfam12730, ABC2_membrane_4, ABC-2 family transporter protein. This family is related to the ABC-2 membrane transporter family pfam01061.	8.71644e-10
NZ_CP045802.1|WP_101808743.1|1564992_1565868_+|YitT-family-protein	gnl|CDD|224203	COG1284, COG1284, Uncharacterized conserved protein [Function unknown].	4.91592e-82
NZ_CP045802.1|WP_153783114.1|1555091_1556519_-|cardiolipin-synthase	gnl|CDD|234967	PRK01642, cls, cardiolipin synthetase; Reviewed.	4.06977e-171

Protein sequences

>NZ_CP045802.1|WP_153783113.1|1553528_1554344_+|ABC-transporter-permease-subunit
MFDFAALVANENMKIYRRPRAWIMLGLLALLAAAIALIASASSSSPLEMWSMTSVMLMLLVPLANIFSVIIAADSVAGEFTGGTIKLLLIRPWTRSKVLLSKYVSVLIFVMFTLLVVYLSVLLINSAVFGYERGVSAEKAFGVLDPGLSAWSYYHQYFLLELISAAVGVTLAFMISAVFRSSALSIGLSLFLLLMGATLSQLLRLVDKPWVDYVLFQHLNLTRYIGSGGASGELHSGSPMTLGFSLAVLAGYYLVFMALSWFVFTKRDVAA
>NZ_CP045802.1|WP_043112008.1|1552573_1553536_+|ABC-transporter-ATP-binding-protein
MLSQPIVQLKQVTKRIGGKTIIDNLSLELPQGEVFGFLGPNGSGKTTTIRMMVGLMRMSEGDIVIGGSSIRTDYEKAIRHVGAIVENPEMYKYLTGYQNLLHYARMVPGISRNRIDEVIRLAGLDKRIEDKVKTYSLGMRQRLGVAQALLHKPSLLILDEPTNGLDPAGIRELRDYLRRLAAEEGTTVFVSSHLLSEMELMCDQAAIIQAGRLIDVRRLRGGEEADAAGIRMPVQMLFEVDRPDEAAALIRDAIRTADGVPAQVQVRSEAGAILLDARRADVAEINALLVRGGILVYGIRSAGKTLEEQFLEVTGGESVV
>NZ_CP045802.1|WP_153783112.1|1552010_1552268_+|hypothetical-protein
MDMKANWQMFHCLCCGQLLRLEAADKLFQTGFYQASYPLGSCTSCRDAKQASSSGLSTSPGGSGSDPGPSSSPSSLLYGCSILSA
>NZ_CP045802.1|WP_127464560.1|1551676_1551910_+|hypothetical-protein
MMRFNDQFHCLSCDRQLPGAEASVLFRTGFYRVDYRLGCCKACEDQAEGGAAADRDGQAPGARDIAHSRFAHYSISA
>NZ_CP045802.1|WP_084137587.1|1550831_1551338_+|DUF1854-domain-containing-protein
MMNGNLVFMNRSKPYEVMLYHSREGYLKAVLGGEPMGRVKLVRCFPYSLPDRLISVRTADTGKELLLLPSLDQLEEESRIAAVMELEREYTIPRIERIVSIRKKGPEWIWSVETDYGPSMLHMSILHEGIHSLADGRWIVTDDDGRRFELSNLDRMDQRSRDQWEKIG
>NZ_CP045802.1|WP_101809435.1|1548720_1550835_+|ATP-binding-cassette-domain-containing-protein
MREGARFTLPHLEAYRIAMPRIAAWLEEPLPVPGGAAPQPPAPGSDAAGASPSAPSGREPHAAPQAGAPQKLPPRVRRGAAQAAAPRGAAVSAEPQGAAEPSRACRVCGKRLWHRRTKCLRCSNKYLMVRRILAYAQPHRRLMIASGVLLLFSIAFELIPTYLMKLLIDNFTEGGSRSALLWLIVAMAAVHLIGTGVSMARSFIGLRFGGRLMGDIRKHAFDAILKLSMSYFDRRQVSQFISRVQNDTEELKQFLTEGFIQFLSQVLLAVGVLGLLFYLNAPLTWMILIPVPFLALGFLWIWPRIRILWYSQWMSVMNVNNVIGESLQGIRVIKAFAQERREKQRFAQANDTLVKRMISMGNLWMSVSPLFSLVIAAFGLLVWYAGGKSVLGGGMTLGSLTAYASYLVMFFGPLQAFGASLNMINRVMGSAERIFELMDAKSDTPDRPDAVQLESAQGEIRFEGVRYGYDKSRAVLKDLNLTIRPGEMIGLVGPSGAGKSTLINLVCRFYDPDAGSIRLDGIDLRDIAQESLRARIGVVLQETFLFDGTIAQNIAYGRKDASPESIIEAARTAGAHGFICGLPEGYETQVGERGHRLSGGEKQRIAIARAVLLDPEILILDEATASVDTETERAIQEALARLVKGRTTIAIAHRLSTLRGADRLIVLEQGRIAETGTHDELYRSKGTYWRLVESQKQMTESEVG
>NZ_CP045802.1|WP_101808730.1|1546440_1547253_+|hypothetical-protein
MNSPAGNLAPMVAALIQKRGAMELTSFGMSMYPLIREGDASRFVRVRARDLEVGDVCLFVSGSGILTGHRLVEIRGEGAGRQYVFRGDTSYVADDPVGPEAILGLWTGVRRARRGGGAGVARIAAAGAGAAKEAAADAAGARAAEGAGAAVGAGTARSAESEADADDARAAKGAVAAVGAGAARSAESEAYADGARAAKGAVAAVGAAGAAPSGTGSRAAEFGGKWITPKHWQARLLRWLVLHYPLTRKFTRKLGTWSMSRKPMYRAASR
>NZ_CP045802.1|WP_028600625.1|1546169_1546448_+|PqqD-family-protein
MTVLANQLLKRQESIETAELDGEWVLLDLESHSITKVNEMGGYIWELLEACPTISQLTERVASEYAADPLQVQADVEAYVAELIRVGLIVHE
>NZ_CP045802.1|WP_153783111.1|1545288_1546173_+|hypothetical-protein
MYLYQAKVGHHRIRFEVQTEHLKEWIAARFPEDRDELAALPVGSGEAAVEAAAGEASESEVVAALASTEAAGAKAVLYITDFYGSMYDEGPVEIEADGDTVVYSRKDYRMETSADYSSVKLQVFDDLALKHALINWYSAWLIHRREGLLVHSSCVVDGGKAWMFVGHSGAGKSTAAELSAPRPILSDEATLLLLDADGGVTIHDSPLRSENEERGEADASPLGGVHFLVQAEEVRREPVGKVEALIGLMDKVFYWKHSKPETAKMIAVCREVVQRVPAYELHFQKNDSFWEVIS
>NZ_CP045802.1|WP_028600463.1|1544777_1544993_+|hypothetical-protein
MKPYCAPAVLGHQSVEFGTVNISNNFFYKWCKSQNFAPFICRLFYGPGGPGGPCGCGTKPLGYLDRYDGAK
>NZ_CP045802.1|WP_153783114.1|1555091_1556519_-|cardiolipin-synthase
MFWLLIALLVFLFQIMTILILEYRQPSKTVAWLLILFVLPVIGFVMYYFIAKEFQNRRTVRRRGVIAREVQLKALRQSALVHRAQDMEAPDFAHEERLFNLLGSFSMLPITGCNETEVLTNAEATYASILDALEGAKHHIHLDYYTLRDDEIGCRFKEALLRKAKQGVEIRIIYDGIGSLELKSWFVKELEEAGVCVQCFLTPRIAFFDKRVNFRNHRKIVVVDGTVGFVGGINIGDEYLGKDPKLGFWRDTHIKLTGDSVYYLQLVFMRDWWFTARERLEKPEYLPEHGCIGEEQVQIVASGPDTSSDAILEGIFSAISAAKEKVYIATPYFIPDPSVLMSLRTAALSGVDVRIILPHGSDSKLVLYSSLSYVEDLLMAGVRIYRYRKGFIHAKVMIVDRLLASVGTANMDMRSFFSNFEINAHVYSAKAISRLEEDFMADLGDCYELTLHEFEKRPRMQKAAEVVAHMLSPLL
>NZ_CP045802.1|WP_028600608.1|1556735_1557209_+|polymer-forming-cytoskeletal-protein
MFKENKRLMAADTLIGQGTRAEGTLSCQASLRIEGEYRGDIECKEDVIVGESGVVRSNISARDLTISGKVYGDVVTTGRLTILSSGQLHGSATTASLLVQDGGVLSGSCRMEAPRPQEAAQPAPAPAPQAARQVQSGEPAPPRELREGVVKERRQAG
>NZ_CP045802.1|WP_146000514.1|1557539_1558244_+|hypothetical-protein
MGDREAKGIKAKEEHEFEEAHAVWLNGHLRKRKGERRDRLKRGHGHGEKLFLKKVWWPMFGSLDELHPEYEVSDWRGARCYLDFAWLRGDLRFNLDVKGYGPHVEQTDRTKYERELLREIQLQTYSFRNVAIPYDTVARDPQLLQQMIRQLLQSLERKPSETSLNLSTTELAILQFAQTQLKDVSPSQVAKAIGIHPSTARHYMKKLVEKGRLIALGKSTCVRRYQYFRDEFRF
>NZ_CP045802.1|WP_028600606.1|1560326_1561223_-|DNA-polymerase
MAVKPEIGEITVEGVTLSITNPSKPLWPEAGVTKLTFLEKLIQLSPYLIRHCRDRHLTTIRYPHGIHDKFFYQKNCPEPRPEFVATRVSGGIDYVVLDKLPTLLWLGNLACLEFHASFDLADDPVHPLEWVIDLDPSQEEEPRIMEAALLVGEQLAALGIESLAKTSGATGVQLIVPLADRLSFDELRSIGQFVGEYMTQKRPDLFTVERLKKHRGDRIYFDYLQHYQGKTIAAPYTPRAKPGATVSTPLGWDEIRAGAQIADFHLLNIAERLQEKGDLLEAAPRQRLRPILEFLRRR
>NZ_CP045802.1|WP_153783115.1|1561244_1562687_-|hypothetical-protein
MGAIRAGGKVGRAGEMGMAGAGSSGAAEADPWPIAGAQAGGAAEAVPWPIAEAQAGGAAEADPSAIAEAQAGGTAEAVPWPIAEAQAGGAAEADPWPIAGAQAGGAAEAMQPMAPIHAAKLPEGPDWGYQIKWDGVRLLATIGGDGGIELFSRNGLRKNAIYPELVELLRSAAPALGPCVLDGELIAWTGERPSFQRVLQRERMRGRSAGSAMTLLRHPDPGVRPWRGGAESAAADAAMAAEEPRSGAKSPGSGQKGEASQSELRHDRPDGSGEPLGLPGLAFILFDLLAYGGTDLRALPYASRHQRLLKLVPLLPDGMLVTELYSDGRALWRWVQEQRWEGVVSKRLTAPYRPAKKHRDWFKTKTALRIDVDIVGLKVREGQVASLVMSLEGQYFGSVSLGLTGEMRTLLTEQLVPDEAFREGSRQHGTLPFPALPSDLKGERIVWLEAPLPGTVTGLEITEAGQLRHPKLAGFGRATS
>NZ_CP045802.1|WP_153783116.1|1562687_1563653_-|Ku-protein
MHTVWKGAISFGLVHVPVKMFSATEDKDISLRMLHSVCGSPIAYVRECPVCDRKIEWDEIVKGYEYEKGRFVTFSKDELEAAAGEKSKTIQILDFVALEEIDPIYFQKTYYLSPDQAGGGAYSLLMEAMKQSGKIGIAKISIRSKSSLAAIRVLEDGCLAMETIFYPDEIRAVSQVPNLPGQVQVSDKELAMAKLLIDQLTTPFEPEKYTDDYRSSMQDLIQGKIAGEDVTVAPRQEPGRVLDLMAALQASLESVKTPAAIPVTDAGAGAAAASGGKRKKAASTGAAGGGKTDSAAESASANGTKKAPKPRVKKKKDAGAS
>NZ_CP045802.1|WP_052333635.1|1563951_1564218_+|hypothetical-protein
MEDGGATSETDAGTGRTNDHGGRMDYEMDIDRMVGEGLGGGQVTIHNGHIGESTTDTMRLKEDIGLDEQEEPDPTERLGRIKSQLMAD
>NZ_CP045802.1|WP_028600603.1|1564271_1564469_+|H-type-small-acid-soluble-spore-protein
MDVKRAMEIYRSSDMFAVHLGGDSVWIENVDEANGMATVQVGTTPQKTKTVSVDRLHEGKPEREH
>NZ_CP045802.1|WP_101808742.1|1564515_1564716_-|hypothetical-protein
MSRNRKKASAKQGASPRQHELDSTRKLWPRKPQTQVGPSRKQQERRTWCRKGRDDGAFPVRAGRPA
>NZ_CP045802.1|WP_101808743.1|1564992_1565868_+|YitT-family-protein
MASVHGQHLRLPLIEVVKRTIFLTIGAILMGVGLEIFLVPNNIIDGGITGISIMVSYLTDAPLGLFLFVLNLPFLFLGYKQIGKTFAISTLYGVAVMSITTFLLHDVDPLTIDEFLASIFGGMVLGVGVGLVIRFGGSLDGTEIVAILFSKKLPFSVGEIVMFVNLFILTSAGFVFSWDRAMYSLIAYYIAYKMIDIVIEGFDESKAAWIISDEHRPIGEAIMSRLGRGVTYLNGEGGFTGGDKKVIFVVITRLEEAKLKSIVTDMDPAAFLAVGNIHDVKGGRFKKRDIH

Crispr_ID: NZ_CP045802_12

• CRISPR_ID: NZ_CP045802_12
• CRISPR_location: 1912979-1913083
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_12

Consensus_repeat	Method
GCGGCTCTAGCCGCAAGCTTTCGC	CRISPRCasFinder

spacers of NZ_CP045802_12

>12.1|1913003|57|NZ_CP045802|CRISPRCasFinder
AGGACGAAAGCAATTGGCGGCTCTAGCCCGCAAGCTTTCGCAGGACGAAAGCGATTG

CRISPR arrays and Neighbor proteins around NZ_CP045802_12

CRISPR arrays

The CRISPR arrays of NZ_CP045802_12

>merge|NZ_CP045802|12|1912979-1913083|CRISPRCasFinder
GCGGCTCTAGCCGCAAGCTTTCGCAGGACGAAAGCAATTGGCGGCTCTAGCCCGCAAGCTTTCGCAGGACGAAAGCGATTGGCGGCTCTAGCCGCAAGCTTTCTC

>NZ_CP045802|12|10|1912979-1913083|CRISPRCasFinder
GCGGCTCTAGCCGCAAGCTTTCGC	AGGACGAAAGCAATTGGCGGCTCTAGCCCGCAAGCTTTCGCAGGACGAAAGCGATTG
GCGGCTCTAGCCGCAAGCTTTCTC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_101808850.1|1905968_1906535_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153783217.1|1917926_1919021_+|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)	unknown	unknown	gnl|CDD|340819
NZ_CP045802.1|WP_153784702.1|1915069_1916236_+|glycosyltransferase	unknown	unknown	gnl|CDD|226988
NZ_CP045802.1|WP_153783218.1|1919993_1920824_+|sugar-nucleotide-binding-protein	unknown	unknown	gnl|CDD|187564
NZ_CP045802.1|WP_101808847.1|1898418_1900179_+|phosphomethylpyrimidine-synthase-ThiC	unknown	unknown	gnl|CDD|236451
NZ_CP045802.1|WP_153783221.1|1924503_1926162_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270302
NZ_CP045802.1|WP_153783210.1|1890651_1897809_+|leucine-rich-repeat-protein	unknown	unknown	gnl|CDD|173801
NZ_CP045802.1|WP_153783213.1|1910056_1911079_+|NTP-transferase-domain-containing-protein	unknown	unknown	gnl|CDD|133019
NZ_CP045802.1|WP_101808849.1|1904906_1905779_+|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase	unknown	unknown	gnl|CDD|180561
NZ_CP045802.1|WP_153783215.1|1913910_1914999_+|glycosyltransferase	unknown	unknown	gnl|CDD|226988
NZ_CP045802.1|WP_028597753.1|1919013_1919997_+|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|367154
NZ_CP045802.1|WP_043111194.1|1913206_1913572_+|hypothetical-protein	unknown	unknown	gnl|CDD|237372
NZ_CP045802.1|WP_153783219.1|1921542_1921941_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153783212.1|1909071_1910082_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153784701.1|1908217_1909075_+|glycosyltransferase	unknown	unknown	gnl|CDD|366154
NZ_CP045802.1|WP_101808848.1|1903638_1904910_+|glycine-oxidase-ThiO	unknown	unknown	gnl|CDD|274092
NZ_CP045802.1|WP_153783211.1|1906762_1907686_+|WIAG-tail-domain	unknown	unknown	gnl|CDD|333735
NZ_CP045802.1|WP_153783216.1|1916279_1917890_+|glycosyltransferase	unknown	unknown	gnl|CDD|340831
NZ_CP045802.1|WP_153783220.1|1922180_1924088_+|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|187570
NZ_CP045802.1|WP_028598130.1|1901667_1902582_+|thiamine-phosphate-synthase	unknown	unknown	gnl|CDD|234590

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_153783217.1|1917926_1919021_+|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)	gnl|CDD|340819	cd03786, GTB_UDP-GlcNAc_2-Epimerase, UDP-N-acetylglucosamine 2-epimerase and similar proteins. Bacterial members of the UDP-N-Acetylglucosamine (GlcNAc) 2-Epimerase family (EC 5.1.3.14) are known to catalyze the reversible interconversion of UDP-GlcNAc and UDP-N-acetylmannosamine (UDP-ManNAc). The enzyme serves to produce an activated form of ManNAc residues (UDP-ManNAc) for use in the biosynthesis of a variety of cell surface polysaccharides; The mammalian enzyme is bifunctional, catalyzing both the inversion of stereochemistry at C-2 and the hydrolysis of the UDP-sugar linkage to generate free ManNAc. It also catalyzes the phosphorylation of ManNAc to generate ManNAc 6-phosphate, a precursor to salic acids. In mammals, sialic acids are found at the termini of oligosaccharides in a large variety of cell surface glycoconjugates and are key mediators of cell-cell recognition events. Mutations in human members of this family have been associated with Sialuria, a rare disease caused by the disorders of sialic acid metabolism. This family belongs to the GT-B structural superfamily of glycoslytransferases, which have characteristic N- and C-terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility.	3.61565e-117
NZ_CP045802.1|WP_153783213.1|1910056_1911079_+|NTP-transferase-domain-containing-protein	gnl|CDD|133019	cd02538, G1P_TT_short, G1P_TT_short is the short form of glucose-1-phosphate thymidylyltransferase. This family is the short form of glucose-1-phosphate thymidylyltransferase. Glucose-1-phosphate thymidylyltransferase catalyses the formation of dTDP-glucose, from dTTP and glucose 1-phosphate. It is the first enzyme in the biosynthesis of dTDP-L-rhamnose, a cell wall constituent and a feedback inhibitor of the enzyme.There are two forms of Glucose-1-phosphate thymidylyltransferase in bacteria and archeae; short form and long form. The homotetrameric, feedback inhibited short form is found in numerous bacterial species that produce dTDP-L-rhamnose. The long form, which has an extra 50 amino acids c-terminal, is found in many species for which it serves as a sugar-activating enzyme for antibiotic biosynthesis and or other, unknown pathways, and in which dTDP-L-rhamnose is not necessarily produced.	6.85794e-108
NZ_CP045802.1|WP_153783218.1|1919993_1920824_+|sugar-nucleotide-binding-protein	gnl|CDD|187564	cd05254, dTDP_HR_like_SDR_e, dTDP-6-deoxy-L-lyxo-4-hexulose reductase and related proteins, extended (e) SDRs. dTDP-6-deoxy-L-lyxo-4-hexulose reductase, an extended SDR, synthesizes dTDP-L-rhamnose from alpha-D-glucose-1-phosphate, providing the precursor of L-rhamnose, an essential cell wall component of many pathogenic bacteria. This subgroup has the characteristic active site tetrad and NADP-binding motif. This subgroup also contains human MAT2B, the regulatory subunit of methionine adenosyltransferase (MAT); MAT catalyzes S-adenosylmethionine synthesis. The human gene encoding MAT2B encodes two major splicing variants which are induced in human cell liver cancer and regulate HuR, an mRNA-binding protein which stabilizes the mRNA of several cyclins, to affect cell proliferation. Both MAT2B variants include this extended SDR domain. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	9.22816e-67
NZ_CP045802.1|WP_101808847.1|1898418_1900179_+|phosphomethylpyrimidine-synthase-ThiC	gnl|CDD|236451	PRK09284, PRK09284, thiamine biosynthesis protein ThiC; Provisional.	0
NZ_CP045802.1|WP_153783210.1|1890651_1897809_+|leucine-rich-repeat-protein	gnl|CDD|173801	cd07475, Peptidases_S8_C5a_Peptidase, Peptidase S8 family domain in Streptococcal C5a peptidases. Streptococcal C5a peptidase (SCP), is a highly specific protease and adhesin/invasin. The subtilisin-like protease domain is located at the N-terminus and contains a protease-associated domain inserted into a loop. There are three fibronectin type III (Fn) domains at the C-terminus. SCP binds to integrins with the help of Arg-Gly-Asp motifs which are thought to stabilize conformational changes required for substrate binding. Peptidases S8 or Subtilases are a serine endo- and exo-peptidase clan. They have an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure and are not homologous to trypsin. The stability of subtilases may be enhanced by calcium, some members have been shown to bind up to 4 ions via binding sites with different affinity. Some members of this clan contain disulfide bonds. These enzymes can be intra- and extracellular, some function at extreme temperatures and pH values.	4.59682e-60
NZ_CP045802.1|WP_153784702.1|1915069_1916236_+|glycosyltransferase	gnl|CDD|226988	COG4641, COG4641, Uncharacterized protein conserved in bacteria [Function unknown].	7.13821e-36
NZ_CP045802.1|WP_101808849.1|1904906_1905779_+|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase	gnl|CDD|180561	PRK06427, PRK06427, bifunctional hydroxy-methylpyrimidine kinase/ hydroxy-phosphomethylpyrimidine kinase; Reviewed.	7.75294e-126
NZ_CP045802.1|WP_153783215.1|1913910_1914999_+|glycosyltransferase	gnl|CDD|226988	COG4641, COG4641, Uncharacterized protein conserved in bacteria [Function unknown].	2.23131e-27
NZ_CP045802.1|WP_028597753.1|1919013_1919997_+|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|367154	pfam02719, Polysacc_synt_2, Polysaccharide biosynthesis protein. This is a family of diverse bacterial polysaccharide biosynthesis proteins including the CapD protein, WalL protein, mannosyl-transferase, and several putative epimerases (e.g. WbiI).	2.65772e-121
NZ_CP045802.1|WP_043111194.1|1913206_1913572_+|hypothetical-protein	gnl|CDD|237372	PRK13386, fliH, flagellar assembly protein H; Provisional.	0.00134375
NZ_CP045802.1|WP_153783221.1|1924503_1926162_+|extracellular-solute-binding-protein	gnl|CDD|270302	cd13584, PBP2_AlgQ1_2, Periplasmic-binding component of alginate-specific ABC uptake system; contains the type 2 periplasmic binding fold. This group represents the periplasmic-binding component of high molecular weight (HMW) alginate uptake system found in gram-negative soil bacteria such as Sphingomonas sp. A1. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that includes alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	1.64147e-174
NZ_CP045802.1|WP_153784701.1|1908217_1909075_+|glycosyltransferase	gnl|CDD|366154	pfam00535, Glycos_transf_2, Glycosyl transferase family 2. Diverse family, transferring sugar from UDP-glucose, UDP-N-acetyl- galactosamine, GDP-mannose or CDP-abequose, to a range of substrates including cellulose, dolichol phosphate and teichoic acids.	3.56164e-17
NZ_CP045802.1|WP_101808848.1|1903638_1904910_+|glycine-oxidase-ThiO	gnl|CDD|274092	TIGR02352, Glycine_oxidase, glycine oxidase ThiO. This family consists of the homotetrameric, FAD-dependent glycine oxidase ThiO, from species such as Bacillus subtilis that use glycine in thiamine biosynthesis. In general, members of this family will not be found in species such as E. coli that instead use tyrosine and the ThiH protein. [Biosynthesis of cofactors, prosthetic groups, and carriers, Thiamine].	4.00416e-88
NZ_CP045802.1|WP_153783211.1|1906762_1907686_+|WIAG-tail-domain	gnl|CDD|333735	NF012201, WIAG-tail, WIAG-tail domain. This 80-amino acid domain occurs in proteins in a single copy at the C-terminus. In most proteins, the domain immediately follows a long, variable run of tandem 10-amino acid repeats. The domain is named for its C-terminal motif, WIAxGx, hence the name WIAG-tail.	2.90726e-17
NZ_CP045802.1|WP_153783216.1|1916279_1917890_+|glycosyltransferase	gnl|CDD|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	1.0007e-29
NZ_CP045802.1|WP_153783220.1|1922180_1924088_+|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|187570	cd05260, GDP_MD_SDR_e, GDP-mannose 4,6 dehydratase, extended (e) SDRs. GDP-mannose 4,6 dehydratase, a homodimeric SDR, catalyzes the NADP(H)-dependent conversion of GDP-(D)-mannose to GDP-4-keto, 6-deoxy-(D)-mannose in the fucose biosynthesis pathway. These proteins have the canonical active site triad and NAD-binding pattern, however the active site Asn is often missing and may be substituted with Asp. A Glu residue has been identified as an important active site base. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	1.96526e-30
NZ_CP045802.1|WP_028598130.1|1901667_1902582_+|thiamine-phosphate-synthase	gnl|CDD|234590	PRK00043, thiE, thiamine phosphate synthase.	1.46588e-84

Protein sequences

>NZ_CP045802.1|WP_153783213.1|1910056_1911079_+|NTP-transferase-domain-containing-protein
MERPARTRNPRRSEAEVKAILLAGGTGTRLRPLTGLMNKHMLPVYQYPMIHYAIHTLAEAGADEILLVTGRQSAGLFIDYLGSGEAFGARLTYLIQEQAGGIAQALDLAKPFIAPQEKFLMLLGDNLVEDSLKPYVEAYRGQEPGTAMVLLKEVPDPHRYGVPVFDSEGGIAAIEEKPANPATSYSVTGIYLYDGSVFDIVAVTQPSGRGELEITDVNNAYARQGKLRYEVLPGWWTDAGTFDSLHEAAGWMKDRMAAAGAGRAAGGADGAGGSAGTDEAGAAAESGEAAEPGEADEAGAGKSVPVEAVPPDDAPTPAATEESAAAMDASPADDDSASQG
>NZ_CP045802.1|WP_153783212.1|1909071_1910082_+|hypothetical-protein
MTKKQASAGRRGAASRPVRRHARRSPRSKRAPASGSRRHRSLAAARRAAARRGGAARSRSARAARLQPAAAGHGWSFPPEAAAVLCSARAESLEAAAAWMEKLGCRKLVLVRCGSGSAEPEAPAGAAELAAEASAADDAGPEAAQRIRLRYPHGGAAAWAAGAAAARQLQPRALLVADADEALQPESRMMLQAVLRAAPERPAAALAEDGGCRRPFSKWSPQTRLNAFLHWSLGGERRTAMSLERTPFALNGAALRRLEDGALLAQPPRALAALLAGGGSALPVRARPSRAASEPIRPLAYADAIRLAGATPRFRYPDHSRDRAAAAGHGEAGTNP
>NZ_CP045802.1|WP_153784701.1|1908217_1909075_+|glycosyltransferase
MPSESRAGNRRQAEADPPPRWRPSGEDASSPLLPPGLLEEDTAPAVSVIIPVMNERRTIAAVLAQAKRVHPRTELIVVSNGTKDGSDRIAARMGAKVLRCARALGHDVGRSVGARAARGEALLFLDGDIVLSAAKLRPFVQAVLSGEADVALNDYSGPTDRSRVHPVVLAKHALNSMAGRSDLRGTSLTAVPHAMSRAAAERIGVEALAVPPLAQVKALAAGLAVRRIVHVDVGRRNRSRLKRERTNPLHRLITGDHLEAAAWLAEAQAKALESGSETREGSGLS
>NZ_CP045802.1|WP_153783211.1|1906762_1907686_+|WIAG-tail-domain
MDMKTNGKPGKASRPFVPGGAPSAKGKAATDSRPRPRRVSRPMYQVDHPDYSELEGLGESPSVDSPHQDTDGRRPGGIRRVKLHGFAAVASPLEGGLVAEELGAREDESEGEGEGEPQRRSRAAFERAGEGDGELARPSAESEPDFHASSRSAAEWARLEEVRFSPALKIRTSPTVRLLPQAMPGGTPEAGADVRSAPPAAAAAQGGPGVSQAGAELAEGPVADGSELQFGTVAFDFKERSRLDLILPLQQPFRDTGYSLACSLDVPFCHAVVRAKLGAEAVVTLIRTQEEGNSRGRLDWIAAGRRE
>NZ_CP045802.1|WP_101808850.1|1905968_1906535_+|hypothetical-protein
MRLVALAAVAAAAGAWLYGYGIMPIWQGGMAAIASDKERYSLDISTLPGEYSMELDLTDLSANVGRDLYRHGDQRIWLSHLEPNSGLLMACFRSDGTVSWSGATLASGLRHARSDSGFGYTLEARMDVQAAGSVYEASGTGMSGINYRKGDMFCYFPFPDKAAEEAAKKEGKALLVVEGLQLHRWTRR
>NZ_CP045802.1|WP_101808849.1|1904906_1905779_+|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase
MRRFKKTLTIAGSDSGGGAGIQADLKTFQELGTFGMSVLTAATAQNSVGVQGVYPLPAEAVARQLDSVLDDIGADAVKTGMLFSADIIGIVAGKLERCGAGPIVVDPVMISKHGSRLLEEKAAEALRTRLLPLAEVITPNLPEACALLGWDESELATEAAMEAAARELLRFGSRHVLLKGGHLPGSAEAVDLLLSADRPDRPERFAAARVPTPHTHGTGCTTASAIAALLALGHELPEAARRAKAFTLKAIQAAGPTGAGTGSLWHAAWRSEPLAEAGAAGSAGRSLPRA
>NZ_CP045802.1|WP_101808848.1|1903638_1904910_+|glycine-oxidase-ThiO
MKERVLILGGGIIGLACAFEAASDGSREVTVVERGGFGGQATGAAAGMLAPFSENVEQPDAFFELCLDSLRRYPEWVERIEERSGMEAGLRRTGSLGVALHEADLLPLQSRLRWQRAAGSGAELLTAAQAARLEPRLAACAGGIYTPAEAHVDAPQLAAALEQACRSVGVRLRAGQGGLASLELRPGDAPECPVALTTERGERFEGDRLVLCAGAWSGEFERLFGLPETIHPIRGQICAYGVPDGEVRHMVFTSQAYWVGKSGGRLVCGASEDVAGFCTDVTDRGIGRLERWSARAFPMLAGMRPSLRWAGLRPATRDGRPLIGRLSGYPQVLFAAGHYRNGILLAPATAAAVLGLLEGDELAASAAFHPERFRRGFSAHPSGAFAPSAGAGTSAPSRAEAAGRGDDAGRTAAAPGGPRRGRA
>NZ_CP045802.1|WP_028598130.1|1901667_1902582_+|thiamine-phosphate-synthase
MKKLDFGLYVITGENYHPGRTLEEVMREALHGGADIVQLRHKTAKKDELLEKARLLRRLTREYGVPFIVNDDPELALEAEADGVHLGQEDGGWREARERLGPDAIIGISTHSLEQALAAEDAGADYIGVGPVFPTETKPGRPAVTLEYVRQASRHVRIPWVAIGGIGPHNAQQVLGAGATRLCAVSAIVGSASPAQACRELKAMIAAARGRRNGQAYEAGRELAAARAAGETNGWAAAAVDIVLNGGPHRTAAGTLERLVEERGLSGRRIVAEADGQIVPREEWSRCRLRRGMAVELVHFVGGG
>NZ_CP045802.1|WP_101808847.1|1898418_1900179_+|phosphomethylpyrimidine-synthase-ThiC
MPILTKPLPGSRKAYIDGKTPGVRVPVREIALTDSDMRGQQVHNEPVRVYDSSGPYTDESYVADIRRGLPALRERWIAERADTEAYDGREVRPEDNGFTDAEKAAAKGAERFPPTGRKPLRAKPGRNVTQLHYARRGIVTPEMEFIALREGMEPEFVRSEVAAGRAIIPANINHPEIEPMIIGRHFHVKINANIGNSAVASSIEEEVEKMTWATRWGADTIMDLSTGKNIHTTREWIVRNSPVPVGTVPIYQALEKVNGKAEDLSWEVFRDTLIEQAEQGVDYFTIHAGVLLRYVPLTAKRVTGIVSRGGSILAAWCLAHHRENFLYTHFEEICEIMKAYDVSFSLGDGLRPGSIADANDEAQFAELDTLGELTKIAWKHDVQVMIEGPGHVPMHLIKENMDRQLAVCDEAPFYTLGPLTTDIAPGYDHITSAIGAAMIGWFGTAMLCYVTPKEHLGLPNKEDVKEGVITYKIAAHAADLAKGHPRARLRDDALSKARFEFRWRDQFHLSLDPERAMSYHDETLPAEGAKTAHFCSMCGPKFCSMRITQDIRDYAEREGLETAEAIEAGMKEQADAFKAGGGKIYA
>NZ_CP045802.1|WP_153783210.1|1890651_1897809_+|leucine-rich-repeat-protein
MSDARWKRSLFSLFALLLLPFQSLTYASHVRLSDSKSLVLTAELSKPDLDLSHLAEQAAKIEGMLDPNEQVKVIVKLKQKSLIDQYSLSSTELSPSQYIQSDAAQREKDLMANEQKIVKSAIASKIAGASFVDSVQYTVALNGFSVELPRKSIENVMRVEGVSSVFEVATYALPDTTAYVSPSLQDAYSSGMIGADLVHSTGYTGKNTVVAILDSGLDTEHEAFKTMPDASSLKYSRDKIAELISGKVLQASKLADIGGNKTYVSDKVPFAFDYANKDTNVRGGMDHGTHVAGIIAGNNTASQTDPSKAFKGVAPDAQLMMMKVFSDGNGSTSDDIILEGLEDAIALGADTINMSLGAAAGFRSTGDQDMDDVYSSVIAAGINLDIAAGNDSSSSVSNTTGLNLNTADNPDTAIVGSPSTVRSALSVASSENVMFSSKYMVVGVTDATYGTEGEASVTLATYIGGVKIPYADVVNANTNAQLPITNTFNDKKLDYVVLDKFGSMEDYQGVDVKGKAVVINRGGGKELTFEQKAVNAKAAGAVAVIVVNNEPGAIVTPAVMNSNIIPLVGVAQNAGEVLANANPMTIYLSKTNESIIENPGGGLISSFSSIGPSPDLKIKPEITAPGGNIYSSMNGNKYQLMSGTSMATPHLAGVSALIRQYLNENPQFSDLSSEGKAKLITNLEMSTASPIKNASGDYYPVRQQGAGLVNVFKAVHSPAYLTVDGERPKAEVGESENGIYSIHFTVNNTSDRTVTYAVYSTALTGKVKSGIYLDTAPRTLRTEEIVVSGDQTVTVPPHGKKDVSLTLALSDTVKQELQQQFKNGIYVEGFVQLESQEEQGINLSLPFLGYYGDWDQPAIFDLPPYAGMPMSPAYTALINQDIYGLVGRLLGENQAATPKTFTDKLAFSTVLADGGRLSSRISLLRNAENMNFSVTSEDGKTEYWHEEYGSARKTYFYANGGSFTTTSPKNAWDGKDKNGKPVPENTKLNYTIKATIAGGTTIQKLVLPFTIDNTAPSITSATTYAENGKTYLELNVADNQNIKYLMFTDTSGHIYALDNYIPEQDGSDITVRVDISNLAEYMQGKGYNPGKIAIYTYDYASNYSIDYVEFGPQTIVMDPAQSVKSGAAVKLHATVKPDKFSNNPVFWSVDDEAVGTIGQDGTFAAKSKGIAVVTAMTGTGLKATTKLYVDTELPDGTGMTETDENLTPPNYINDSQHGNLSVAGNHAQIVANLNEVFRADGLDYRVTGHHEVQLIADQTVDPTSFVARYPDKKGEIILPKAIEHGGEEYSLTSIGYRAFYFASNVERVIVPDGVKIIGEQAFNSAFKLTKVILPDSVERIDDEAFSWLGNAEINIPKNVKFIGRYAFAGNQKLKEVILNPGFQELGYSALGMTSVTKVHLPDGVKGIGENAFINTSKLSEIRLPGDLKRIPRAAFYGSGITSIELPQGLEAIGPSAFQLSKLTSVTIPSTVTRIEAFAYSDLNAKLADVIIPDSVQVMGEKAFRGLTSKSILVGANALRIDRDAFIGAKTNVIAANKTVARQIRRSNYSASITVGGSEFADYVPGLFLADGILYRPTSDTTAEVQALDNKTVSELFIPEQATDSGNNLTYTVTSIAAFLTKGVPTLTKIVLPDTIEIIGERAFDQNLYLKSFNYPKKLKEVGFQALGYSGQQEPGYNGGVDLEIPQSIEWADDSGFAGIKETEITVPAGPTFVNEYQFAAMNNLKKIVMGNSITAINRGGFSGAKALTSVDLPDSLVYIGDEAFSNSGLTSVAIPNSVRYLGSRAFNQVKEARLGGSVDAFGWRTFSNDAQLSVVLNSQREDLVKFNTLERLPALKWDGSTTIPTLDSSIVPAEAVATITTDRSTRAELNPNHAQVSTSIYGKLIVDGSLIIPEDEVLFLSGDLVVNGKVTGKGTIRYAEGATFDKSRIDPTVTVISDEEANNPHIPTPTPSPTPTPSSTPSSTPTPSPAPSDPGIPTASPAPSVQPSPVISNTEHAIRSTETVQDGMMMVTVTDADLTAAIASAGNSIESLVISTNKEQAKLVLTGRQVELLSALPKKSTVVFSAGGSSVVLPLSLMSLAPSNSSLELEIKPAADSSAFVTALGNGKLIGQPVSFEADWTTAAGRKPVDIPNHLFITRTFTVPGSFELDEAGVLYEEDGAVSPVASILSKQADGTTKVTVSRPGFSVYALATRTVNFTDLDDSAAARVIEALAGKWIINGTSATTYSPDASLSRAEFTALLVRALGLKSTALASFTDVKKGDWFAADVAAASEAGLIQGIGKGKFAPNDKVSRQDLAVILERALKLAGIELTTDQTVAYTDLAHAAAYARESIQKLTDAGVLNGYLLSGKTYYQPNAPADREFAAVALYQWLLKAKLMNGLDLS
>NZ_CP045802.1|WP_043111194.1|1913206_1913572_+|hypothetical-protein
MAILLLAASKPATRRMKPKTAAGAKKTTTRTGGKRKKASGTIRRKAKSAAGGKGARPRRRAAAARPRRIRRIRRAPLQAVPQMAGSPSYVAGFQQTYNEGYQLGFGQGYEEGLQLAYETQP
>NZ_CP045802.1|WP_153783215.1|1913910_1914999_+|glycosyltransferase
MASQEQLLAAGRAAGRIAGEAHGRRDGACRSAAQTVAPAAYPQRPLTVLFVPQGFPAIDEGVADALRQHASTVHVGHPSTMLAQAAELRPQLVLVMNGLHVFPPDHAEQIAAIRALGIRTAIWFADDPYFTRETARLAPLYDAVFTHELEAVPFYRASGANAHYLPLGANPTVFHAKPVGQEYRSDVFFVGTGFWNRIRLLDEVLPALEGRKVVLAGGEWERLDRYARYKPFIRPGFMPIEETVNFYNGAKIVLNIHRTTEPGSDNHNDAGLRGASINPRTYEISACGTLQLTDIRDDLRRYYEPGRELDVFTTPAELTAKILHYLDHEDERRRIAVRGMLRTMRDHAFAGRLGMLLDRAGC
>NZ_CP045802.1|WP_153784702.1|1915069_1916236_+|glycosyltransferase
MRGKRIRPSRQKRQAAASVRRSAPPLLDAEVQRGREAGFAAGMEHGLWYGKCEAGLSRLQYAPPVFPIHVLFVATAKGYPYSPLDSAIADTLRSMTARVSITDTQQPVVQLAKELRPDAVIVLDGLQYPTEQVDAIRALGIRTAVWFTDDPYYSDITRKLAPHYDFVFTLESNTVEFYRQLGCPNVTYLPLGVNPAEFRPRNPDLSLRREISFVGSAYHKRVDFFNQITPYLATRDIAISGLWWERLRDFRLLQSKIRAGHWMDPMETAATYNGAKIVINMHRAHDDETFNSNSAQLTAISPNPRTFEISACGTLQLTDVRDDLARFYEPGVEIATYASPQELVEKIDYYLNHEEERQAIAFRGMCRTMKEHTYAHRLTTMLSVMFPS
>NZ_CP045802.1|WP_153783216.1|1916279_1917890_+|glycosyltransferase
MSMEFRPRLLFFSHIGSPEAITGAEKLLLSTIVELSAVADCTLAVPEEGILSGRAAAAGIPVRVTGHVPIYYSMYLGLPSVPEEVEEGTGSEAMERLYRLLLEIRPHAAWVNTCVQPLPAIAAKRLGIPVIWCLTETMRPAAGVGPTMKLIEQHADRVVGISASTLKPLASPLALSRSEVLLPGVDTAAFKPWTWASSRAVRRAELGLQEKQVLIGFIASHLYENKGLEHFLAAAGMAAASRPDLRFVVIGNPVDAEYAARCARIADAAGLSARLSWLPFEPDVSRAYPAMDVLVVPSIVEEGFGMTALEGLLFGKPVVAYASGGLAEILHATGNADWLAPMGDYAGLAERIGRLADNAPLRLATGTRSGAAALAVFGMPAFRGRLLASLERLRLPREPESRIAHGSGPERGLLAGWTLRPIASPEAEASAGLGGVPRVQLPDGVLALLPRGEPIGSPPAEPAAAAEPPAPASPSLAGGRRERLRRKGRLRRGKAGRARRARRGERSRPARRRRAGGASRRRKIGSAGRRAGRKKR
>NZ_CP045802.1|WP_153783217.1|1917926_1919021_+|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)
MRVMTVLGTRPEIIRLSLIIGKLDRLADRHILVHTGQNYTDSLNDVFFRELGVRRPDHVMAGGSHTLGGQLSVMFGEMERLLREERPDIVLLLGDTNSALCAIVAERMGIPVAHMEAGNRCYDLTVPEEKNRRIIDAVATINMPYTEYSKQNLLREGFPANRIVRTGNPIGEVMAQYKDRIDGSGVLERLGLQERDYVLVTTHRAENVDVPAHLDGILGGLNRIAERHGKRIVCSIHPRTRSRIDAGGTAVQPHPLVEFHEPFGFFDFVRLERDAWCAVSDSGTVQEECCLLGVPTVTIRNTTERPETVDCGSNVVSGLRAGNIADAVDVMTALPASWGIPAGYEALDVSDIVVKYVLGGKWNV
>NZ_CP045802.1|WP_028597753.1|1919013_1919997_+|NAD-dependent-epimerase/dehydratase-family-protein
MFENSRILVTGGTGSWGHELIRQLLPQNPKEIIVFSRSESAQVTMSRMFEDARLTFRIGDIRDLEALTKATQGVDYVFHLAALKHVPVCEEHPYEALKTNVLGTQNVIEAANLNKVKRVIYISTDKAANPSNFYGMTKAIGEKLIVYANLVSTDTKFVCVRGGNVLGTNGSVIHLFTNQIKTKGQVRLTDRGMTRFFLTLHDAISLLFKASEESLGGEIFVMTMPTCRIEDLAEVLMEDIGVQAEVVETGIRPGEKLHEILLTEFESKSTVIYDKEYLVILPPLDIPGLQQRYSTYDAVDFDSFCSSENLMDKEQIRDMLRRGGFLQ
>NZ_CP045802.1|WP_153783218.1|1919993_1920824_+|sugar-nucleotide-binding-protein
MRLLVLGGGGMAGSMMVDYFRGRDGFELSWTTRGGGDGSLPLDASDLEAVRRTVAAVRPELIVNCIGKLNADAEAHPLEAYAVNGLLPHWLAFAAGEIGARLIHISSDCVFLGDRGGYTELDRPDGISVYARSKALGEVNDPRHLTIRTSIIGPDASPKGIGLLRWFLAQTGEVSGYSRVYWNGVTTLELAKAVEHAAAHPEIGGLVHLLAAAPASKLEMLEWFKEAYGRDDVAIVPAAEPEIDRTLSAVRTDWIYRAPSIPDMVRELAAWERRGG
>NZ_CP045802.1|WP_153783219.1|1921542_1921941_-|hypothetical-protein
MNQFFRKAGKIGGKGLLIGVLATFALVCIFGIVFFVGLWFGPGKDDIALFHGNKYAISKSPMSYDLYEKDKVLILPNVTSYYVGKEKSYIFNNSDVVIIDEKHGNYEKKDLNDATLEEQSFIEKALEIRPSQ
>NZ_CP045802.1|WP_153783220.1|1922180_1924088_+|NAD-dependent-epimerase/dehydratase-family-protein
MMNYIIFRTKQPRNIDARCWLLLHVNRSRGWPIVPVLERAISWRRQKKDATSMFSTHSAFLDTSAYGRSSAPEVTFAARAFIQRIGPGKQRYEANDEGREGRGRMIGKGTSRREISDSGSSSRSIGGTSGPKGAEASNWRRSSSRRLKKETSGHETGGSAGCRLEEGAAGERSEAGSSGRRKRLLVTGAGGFCGSHAVRHFARAGWEIVACVRPGSTPFWADPAKRPDWFVAADAVDATDAMNVMDAVGATDAVNAADSVDAPGAEAGVDSSDVLNASDVSNSLDAPDALDASNAVDHADASDDGAPGSSSLAFASRPGRDEPEWLSLVRLEALDLSEPGSDSLSELLRRTRPDAVLHLAGLNAAGPSWADPSGYLDLNLMGTVRLLEAVRASGHPCRIVVAGSMLGGSADGPPPVKPLHPYALSKAMQAQAALGWHALYGLDVLVAIPSNLVGPGPSAGLSRLLARYAAACERTAAQAGNSAEAPPASDPSLPGRSDAADPSLPGRSDAVADLAPSAAAETQAPPPFRLSSATEARDFLDVRDAMTGYETLLERGAAGRSYAMASGRMTPLGELAELYRELAAVPLPMEIGGSTAASPEPIDASALRALGWAPRIPLRQSAQDTLEDCRAAGSA
>NZ_CP045802.1|WP_153783221.1|1924503_1926162_+|extracellular-solute-binding-protein
MNRWLKSGLSLALAGALLAGCTSGGGNNGNNAGSGGQTGGAGADGQGAAGAAEQTAYPLQTDKQLAYWAELPGNLVGVQPSLDEVPFFQEWQKRTGVKLEFASPPSGQAKESLNMLLASGDLPDLIEFNFLDGFPGGPEKAIKDGYILRLNDYIDKYAPNLKRFLQDNPDIDKMVKTDSGSYYAFPFIREDEYLRVFQGPIIRQDWLDELGLPVPETIDDWTATLRQFKEKKGAAAPLSFVSKPRFFQESGNGAFLGAFGVTRGFYQEDGQIKFGPSEPGFKDYLELFRGWYAEGLIDKNAATADGKALDGNIVSGAAGATVANAGGGIGKWQPLVQAKDPKAVLAAAPYPVLNKGDKPKFGQRNNAYSPEGIVAVTTSAEDPELAVRMLDFGYSEEGRLFFNFGTEGVSYEMKDGYPTYTDLLMKNPDKLAPAQMISQYARGSYNGPFIQDKRYAEQFFALQTQRDAVELWQQTDSASYNLPPITPTAEESSEYATIMNDINTLVDEMTLKIILGSEPLDAYDDYLAKMKSLRLDRAIEIQTAALARYSSR

Crispr_ID: NZ_CP045802_13

• CRISPR_ID: NZ_CP045802_13
• CRISPR_location: 1973780-1973856
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_13

Consensus_repeat	Method
GCAATTCGGTCGTGGGTGCACCAGTT	CRISPRCasFinder

spacers of NZ_CP045802_13

>13.1|1973806|25|NZ_CP045802|CRISPRCasFinder
GGAGGAGAGTTACTCGGTTTTCCGA

CRISPR arrays and Neighbor proteins around NZ_CP045802_13

CRISPR arrays

The CRISPR arrays of NZ_CP045802_13

>merge|NZ_CP045802|13|1973780-1973856|CRISPRCasFinder
GCAATTCGGTCGTGGGTGCACCAGTTGGAGGAGAGTTACTCGGTTTTCCGAGCAACTCGGTCGTGGGTGCACCAGTT

>NZ_CP045802|13|11|1973780-1973856|CRISPRCasFinder
GCAATTCGGTCGTGGGTGCACCAGTT	GGAGGAGAGTTACTCGGTTTTCCGA
GCAACTCGGTCGTGGGTGCACCAGTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_101808877.1|1963515_1965099_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|381091
NZ_CP045802.1|WP_153783242.1|1983584_1984430_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223472
NZ_CP045802.1|WP_153783235.1|1969321_1970146_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223472
NZ_CP045802.1|WP_101808879.1|1967062_1968352_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_CP045802.1|WP_101808889.1|1985145_1986465_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153783241.1|1979312_1980887_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270452
NZ_CP045802.1|WP_101808874.1|1959368_1960085_-|glycosyltransferase	unknown	unknown	gnl|CDD|133055
NZ_CP045802.1|WP_101808875.1|1960295_1961126_+|amidohydrolase-family-protein	unknown	unknown	gnl|CDD|226145
NZ_CP045802.1|WP_153783233.1|1961305_1963285_+|glycoside-hydrolase-family-127-protein	unknown	unknown	gnl|CDD|226063
NZ_CP045802.1|WP_101808887.1|1982649_1983552_+|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP045802.1|WP_153783240.1|1978513_1979488_+|substrate-binding-domain-containing-protein	unknown	unknown	gnl|CDD|380661
NZ_CP045802.1|WP_153783238.1|1975101_1976709_+|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_CP045802.1|WP_101808886.1|1981159_1982542_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|274816
NZ_CP045802.1|WP_101808873.1|1958998_1959244_+|DUF2164-domain-containing-protein	unknown	unknown	gnl|CDD|378315
NZ_CP045802.1|WP_153783234.1|1968434_1969325_+|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|224096
NZ_CP045802.1|WP_153783237.1|1973972_1974947_+|hypothetical-protein	unknown	unknown	gnl|CDD|131944
NZ_CP045802.1|WP_153783236.1|1970168_1973216_+|DUF4981-domain-containing-protein	unknown	unknown	gnl|CDD|236548
NZ_CP045802.1|WP_153783239.1|1976705_1978499_+|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|225519
NZ_CP045802.1|WP_127464541.1|1984552_1984846_+|hypothetical-protein	unknown	unknown	gnl|CDD|379248
NZ_CP045802.1|WP_101808878.1|1965095_1966871_+|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|225519

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_101808877.1|1963515_1965099_+|response-regulator-transcription-factor	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	6.09889e-55
NZ_CP045802.1|WP_153783242.1|1983584_1984430_+|ABC-transporter-permease-subunit	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	4.65247e-81
NZ_CP045802.1|WP_153783235.1|1969321_1970146_+|ABC-transporter-permease-subunit	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.35566e-68
NZ_CP045802.1|WP_101808879.1|1967062_1968352_+|extracellular-solute-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.86512e-42
NZ_CP045802.1|WP_153783241.1|1979312_1980887_+|extracellular-solute-binding-protein	gnl|CDD|270452	cd14749, PBP2_XBP1_like, The periplasmic-binding component of ABC transport systems specific for xylo-oligosaccharides; possesses type 2 periplasmic binding fold. This group represents the periplasmic component of an ABC transport system XBP1 that shows preference for xylo-oligosaccharides in the order of xylotriose > xylobiose > xylotetraose. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	5.71672e-57
NZ_CP045802.1|WP_101808874.1|1959368_1960085_-|glycosyltransferase	gnl|CDD|133055	cd06433, GT_2_WfgS_like, WfgS and WfeV are involved in O-antigen biosynthesis. Escherichia coli WfgS and Shigella dysenteriae WfeV are glycosyltransferase 2 family enzymes involved in O-antigen biosynthesis. GT-2 enzymes have GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	2.12736e-36
NZ_CP045802.1|WP_101808875.1|1960295_1961126_+|amidohydrolase-family-protein	gnl|CDD|226145	COG3618, COG3618, Predicted metal-dependent hydrolase of the TIM-barrel fold [General function prediction only].	2.271e-63
NZ_CP045802.1|WP_153783233.1|1961305_1963285_+|glycoside-hydrolase-family-127-protein	gnl|CDD|226063	COG3533, COG3533, Uncharacterized protein conserved in bacteria [Function unknown].	0
NZ_CP045802.1|WP_101808887.1|1982649_1983552_+|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	5.972e-68
NZ_CP045802.1|WP_153783240.1|1978513_1979488_+|substrate-binding-domain-containing-protein	gnl|CDD|380661	cd20006, PBP1_ABC_sugar_binding-like, monosaccharide ABC transporter substrate-binding protein such as CUT2. Periplasmic sugar-binding domain of uncharacterized ABC-type transport systems that share homology with a family of pentose/hexose sugar-binding proteins of the type 1 periplasmic binding protein superfamily, which consists of two domains connected by a three-stranded hinge. The substrate specificity of this group is not known, but it is predicted to be involved in the transport of sugar-containing molecules and chemotaxis.	4.99242e-103
NZ_CP045802.1|WP_153783238.1|1975101_1976709_+|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	4.06811e-57
NZ_CP045802.1|WP_101808886.1|1981159_1982542_+|extracellular-solute-binding-protein	gnl|CDD|274816	TIGR03851, chitin_NgcE, carbohydrate ABC transporter, N-acetylglucosamine/diacetylchitobiose-binding protein. Members of this protein family are the substrate-binding protein, a lipid-anchored protein of Gram-positive bacteria in all examples found so far, that include NgcE of the chitin-degrader, Streptomyces olivaceoviridis, and close homologs from other species likely to share the same function. NgcE binds both N-acetylglucosamine and the chitin dimer, N,N'-diacetylchitobiose. [Transport and binding proteins, Carbohydrates, organic alcohols, and acids].	1.34126e-66
NZ_CP045802.1|WP_101808873.1|1958998_1959244_+|DUF2164-domain-containing-protein	gnl|CDD|378315	pfam09932, DUF2164, Uncharacterized conserved protein (DUF2164). This domain, found in various hypothetical prokaryotic proteins, has no known function.	1.17641e-17
NZ_CP045802.1|WP_153783234.1|1968434_1969325_+|ABC-transporter-permease-subunit	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.49834e-83
NZ_CP045802.1|WP_153783237.1|1973972_1974947_+|hypothetical-protein	gnl|CDD|131944	TIGR02898, Uncharacterized_lipoprotein_YlaJ, sporulation lipoprotein, YhcN/YlaJ family. YhcN and YlaJ are predicted lipoproteins that have been detected as spore proteins but not vegetative proteins in Bacillus subtilis. Both appear to be expressed under control of the RNA polymerase sigma-G factor. The YlaJ-like members of this family have a low-complexity, strongly acidic 40-residue C-terminal domain that is not included in the seed alignment for this model. A portion of the low-complexity region between the lipoprotein signal sequence and the main conserved region of the protein family was also excised from the seed alignment. [Cellular processes, Sporulation and germination].	6.33072e-14
NZ_CP045802.1|WP_153783236.1|1970168_1973216_+|DUF4981-domain-containing-protein	gnl|CDD|236548	PRK09525, lacZ, beta-galactosidase.	0
NZ_CP045802.1|WP_153783239.1|1976705_1978499_+|HAMP-domain-containing-protein	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	1.7195e-67
NZ_CP045802.1|WP_127464541.1|1984552_1984846_+|hypothetical-protein	gnl|CDD|379248	pfam13540, RCC1_2, Regulator of chromosome condensation (RCC1) repeat.	0.000235713
NZ_CP045802.1|WP_101808878.1|1965095_1966871_+|HAMP-domain-containing-protein	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	5.84847e-49

Protein sequences

>NZ_CP045802.1|WP_153783236.1|1970168_1973216_+|DUF4981-domain-containing-protein
MSDRQASLDWLADPAVFKVNRLDAHSDHRYYATVEEAEAGAPMKMRHSLNGSWSFHYAANPASRPADFHAEGFSTAGWGDIQVPGHIQLQGWGQPQYVNTMYPWDGLEAIRPPQLPEHNPVGSYVKEFELPADWAGRPTFISFQGVESAFYVWLNGEFVGYAEDSFTPSEFDLTPHIRGGANRLAVAVYQRSTGSWLEDQDFWRFSGIFRDVYLYTTPDIHAVDLEVRADLDDTYRLGTLHASIRLADAAPAGSYALLRLRDPQGAVVAESGQVALDAAGRIAAVLEAGEVQPWSAELPRLYSLLVTIHRPGGELVEAIVQKAGFRRFELKDKLMLVNGKRIVFKGVNRHEFNSRSGRAIGKEDMLRDIRILKQNNLNAVRTSHYPNQTLWYELCDEYGIYVIDEMNLESHGSWQKMGAVEPSWNVPGDLPQWQDIVLDRAASMLERDKNHPSIVIWSCGNESYAGEVILNVSNYFRERDPSRLVHYEGVFHNRAFNDTSDMESRMYAKPADIEAYLNDDPQKPYISCEYMHAMGNSVGGMHKYTELEDKYPLYQGGFIWDYMDQALIRKDRYGKEYLAYGGDFGDRPTDYSFCGNGIVHADGTVSPKMQEVKFLYQNYRLTPSLDSISVRSGSLFAGTGHLELACRLLRDGALVHEAIVPLEVGPGEEAEVPSGLPQGIAEAPGEYVIEASLRLRDDQLWAAAGHEVAFGQSVVRVEREAAEPLPAGEIDVVEGDVNIGVFGRGWQALFSKQAHSLVSLRYGGREVIESPPMPLFWRATTDNDKGTALAYTHGAWLAASVARRCTGWELTQEAGTVTVAYRYEFSTAPGAWLTVAYTVRADGSIRVRTEYKGAQGLADLPILALTFKTSADYGQTKWYALGPEENYSDRCHGARLGTFSRAVAELPSRYLVPQESGNRTGVRRLDVLDAQGKGFAVAAVSEPLECNVSPHSAMELENAAHVWELPAVHYTNVTVAAKQLGVGGDDSWGAPVHPEFRIPSDRDYAFEFILEPSRK
>NZ_CP045802.1|WP_153783235.1|1969321_1970146_+|ABC-transporter-permease-subunit
MKSLKRTPIYLFLTLAAGVSIFPFLWILSSATNKSIDVSSGRLLPGSNLLNNFRNLTEQVELGQAMWNSAKISVTTTLLALLIASLAGYGFEIYRSKAKDIVFNILLLSMMIPFAAIMVPLFQMFAGISGFAPAIGINTIASVILPTFTTAFLIFYFRQSSKMFPKDMLEAGRMDGLSEWGLFFRIYVPTMKTSYAAGAIITFMSSWNNYLWPLVVLQTPDKRTIPLLISNLGSSYSPDYGIIMTAIVVSTLPTALVFFLMQKHFVAGMVGSVK
>NZ_CP045802.1|WP_153783234.1|1968434_1969325_+|ABC-transporter-permease-subunit
MKQTAIVRNRLQPRWTGWMFISVAVLMILLFYFYPMLQALLLSFKSGTGARIDWTGLDNYKRLTSDPVFWTALKNTFLYLIVQVPVMILLAMFISVLLNDSKLRFKGFFRTAIFLPAITSLVAYSVVFKYLFGAEGLVNQALLKLHLIDAPLQWITDPVLAKITIIIAITWRWTGYNMIFYLSALQNIDASIYEAARIDGASPVRQFFSITTPMLKPIILFTSITSTIGTLQLFDEIMNITKGGPGNATMTISQYIYNLSFKYTPDFGYAATVSYTIVILIVLLSILQFKAAGDKR
>NZ_CP045802.1|WP_101808879.1|1967062_1968352_+|extracellular-solute-binding-protein
MKKQMAFAALAGVMALTACSSGNNDGQEGQSSGGGKVTVWAWDPNFNIAAMKLAKEAYAAENPDVNVDIIEYAQADIIQKLNTGLNSGTTSGLPNVVLIEDYRAQSFLQAYPDSFYKMSDLIKPGDFADYKLSSTSLDGVQYGVPFDSGVTGLYVRKDLMEQAGYSVDDLQNIDWDQFIEIGKAVKEKTGKAMLTQDPNDLGLIRMMIQSAGAWYTAEDGTTPDLKDNAALKDAFATYKKLMESDTVKMISDWSQFLAGFNTGDVATVPTGNWITPSVKAEASQSGQWAVVPMPKLKNTASSVNASNLGGSSWYVLNVDGKEQAAEFLAKTLGSDAELYQKLVTDIGVIGTLKAATEGDAYNQEDAYFGGQKIVSDFAAWTQKIPQVNYGMHTYAIEDILVSAMQSYLGGADLDKVLSDAQSQAESQLG
>NZ_CP045802.1|WP_101808878.1|1965095_1966871_+|HAMP-domain-containing-protein
MKEAGGRLSRLGLFGKMFIIMVISTIAVGGMTSWVTVHVSQQLFLDTFSLTNAKVVSQIKRNFESFHYSILTASNEAMQNSTIRSFLTEEEGNSLSENKAYYAMVAQMTRIAAGLDQNEVGTIILGDGERSYFSDRSYWTKSAAALKRQELAAEQPQNASRLTYRLLLEQDGTAGEPILTASRKLISRTTGLPYGTMLFMLPERDFSRFYSTFTSTGNDVLVLDRDGMIVSSNLTGRIGSRDAALLAGAERIRAEGLDSISIGSGEGSQLMVSQHLPEYDFYIVNLVDKKLVRDMLPVTQIVLIGAAIVSAALLILLLISRRLTRSLRLLVRQMSSVTKRNFHNYMPVSGSYETRQLGTAFNYMLDELNAYIMQLVQTQREQRNAELAALQRQINPHFLYNTLASVNFLVQREDKQKATETIHALISLLQNSIGNVEETIPVEQEVQNLKDYAFINGIRYGSGIAVDYFISPDCLQAEVPKLILQPFMENAFFHAFKERESGYIYVIVAREGESLLCEIVDNGDGMDLQDGQDSLPDSQSNRQLFSGIGIRNVHARILLLYGKDYGVTIRSKPGEGTRVQVRLPFAEKSEG
>NZ_CP045802.1|WP_101808877.1|1963515_1965099_+|response-regulator-transcription-factor
MSELTCNVLIVDDELLARQGIKHLLDWESEGFRIVGEAANGKEALELIERLSPHILITDIVMPVMDGEELAREVRIRHPEIRMIVLSSFSEFDYVRSTFQSGVEDYILKPKLDAGKLLATLKKMAAGIPELSGIRLGGAKQQSLRALLDKAAAGFPLGDSMDGARLLQEQLPHRSYAVFGARLDGDSPAAGTAAWKERLEAHLAELPAAGRFAPAAELAEGRDLVRALINFDAADLPLLEAWLERLEASAAEGSWPVLGALGPAFGSLGGLHAAIEQLPALMERRFFRPERRFFAPPAQAAAASGGSAFDAAAFEAELGGQQFEAAFARLRQFASSMEGCEGMRVQELKSFLGHHLFHVIVALLRHQYPAASLDERKYEYFREIHEARSVQEAERTLLRFLDEAEGCVAARQRPGGSQAMQKLLAYIHEHYAEPLHLADVAQHFHFNPSYLSNYFASRNKEGFSEYVNRVRIEQACRLLADTDDAIADIATRVGYADNSYFTKVFRKYMDQSPSQYRRSAQEGKDLR
>NZ_CP045802.1|WP_153783233.1|1961305_1963285_+|glycoside-hydrolase-family-127-protein
MKQAAAAGTKERVRIKDGFWDAYAALVRDTVIPYQWEALNDRIADAEPSYAIRNFRIAAGQEQGEFGGMVFQDSDLAKWLEAVGYALGTHPDPELERIADEAIELVAAAQQEDGYLNTYFTIKEPGKRWTNLYEAHELYCAGHMIEAAVAYYEGTGKRRLLDVVSRFADHIDSVFGREEGQLRGYDGHQEIELALVKLYGATGERRYLDLAKFFIDERGAEPNFLVEECGRRDGVSHWTGRQQPIPSVRQMAYNQAHKPVREQDVAVGHAVRAVYMYTAMADLAGLTGDAELLESCRRLWANMTGKQMYITGGIGSTHHGEAFSFDYDLPNDTVYAETCASIGLIFFARRMLQLEPKSEYADVLERALYNNVIGSMSQDGKHYFYVNPLEVWPKASEGSPDRRHVKAVRQKWFGCSCCPPNVARLLCSLHDYVYTASAEDDVVYAHLFIGSEARFELKSGTAAFVQTSLLPWQGGTRFEWTEAPETAVSLALRVPSWCAGQALLKINGAESAYRTVDGYAVLTRVWAAGDVVEWEPRLEARLIAANPEIRADAGKAAIERGPLVYCLEEVDNGAPIASLSIDPDTELIPTFDAALPGGAVSLEAAGRRADLAGWDPDQPYRPLGQAPEPVAAELRAVPYFLWGNREPGEMAVWIRLSRV
>NZ_CP045802.1|WP_101808875.1|1960295_1961126_+|amidohydrolase-family-protein
MRIDAHQHYWTMSRTDYGWITPDLPVLYRDYLPEDLEPCLQRHGLDGTIVVQAAPTAEETEYLLSLADRSESILGVVGWLDLFDPSHRARYEAYRSHPKFVGFRIMIQEMPDAARVLEPSFVQALRELAREDVPVDLLVKSTQLDALNALLDAVPGLRGVVDHIGKPRIAEQAFEPWAAQLARAAEHPAIYCKLSGMVTEADHQAWTPEHFRGYVEHVLSVFGPERVLFGSDWPVCLLAASYDQVVDVLESSLPAHWGAEERARLFGGNAREFYKL
>NZ_CP045802.1|WP_101808874.1|1959368_1960085_-|glycosyltransferase
MLPLVTVVIPFYNCPYIPQAIQSVLDQSYPSIELIVVDDGSTTNQHLLDPYRHRIVYLSKANGGTASALNYGMQCASGRYVAWLSSDDLFTRDKVLNQVSYMLEKNAQFSFTDFHTINETGQITQMWSMVKFPTEKAFIASMLDFCPVNGCTVMMLRDLIQNVGWFNPGLPYAHDYDLWARIALNDVGMHYLNEPLTLYRRHAGMGTVQHLSRIMPEFESLKAYYAPMLRTKLARMPG
>NZ_CP045802.1|WP_101808873.1|1958998_1959244_+|DUF2164-domain-containing-protein
MMPIKLPLEQKKELAEQLRDFADRELDLPLGTIGAEALLDHMIAALAPHLYNKGVEDALKLLGQRMLQVEDDLHALKRTIR
>NZ_CP045802.1|WP_153783237.1|1973972_1974947_+|hypothetical-protein
MKHPWKVLAAGVALSTALAGCGTHHGELGNKNIRNNNIGNYRLLDKRFADDNMNEMNRVDGRQLNGNNIIGNHRNYNLKSNRQIAGTVKKLEGVRDAYVLTTNDNAYVAVGLKGESIVGSTNTRSGTEMGYAASNTGRMGSNSGRMSAKSGDGLSLERGMKRLDGSMGRMNERLGRGMDGKFDNTIDQYGRMGESRGNNGYISLSNGYNGYGGASATNRRGHMENGLADNNNIYMARSLNEGFKTQVADAVRKSMPGIDKVFVSANPDFFSRMREYDNDAKQGHSIQPYLAEFNAMVERVFPNVDDGSAGTQKKLSGLDAHIFK
>NZ_CP045802.1|WP_153783238.1|1975101_1976709_+|response-regulator
MYKLILVDDEPIVREGLMNTIDWASHGFELAGDYANGRDALEAVELLRPDLVLTDINMPFMDGLELSAAISASHPNVKIIILTGYDQFDYAQQALRMKVYDFILKPITASETRELLDRLRGELDEERRRKEDVDRLRSQLSQSLPLLRERYLDRLAATGAGSQDAEERLAYFGLPPLQPPLLALLLDFDGGPAAGSEPDRELLRFAGFNIAEEIAAREGAICFRTREERIAVLLSGQPPADLYEQASRIAWSIRREIEHYLGYAMSAAFGRAADSLAKLPESYRSAIAALDYRFHYGRDRVLSIVELEGERAAPPAAGEDWSGKLGAALRSGSAGELRQLFGDFTERLKQSRAPLVSCQLEIQRALVTMLSVLQEMGVEESGLGDSPGMLFAEAQRLSTLDEVGGWLTDLATRGAKAAADSRSRLGRSQIGQALLYIERNFADERLSLSDICRQALMSTSYFSQMFKQETGETFVEYLTRVRMAKAKELLEATPLKLYEIAAQVGYSDPNYFSLAFKKHAGLSPREYREQARGQA
>NZ_CP045802.1|WP_153783239.1|1976705_1978499_+|HAMP-domain-containing-protein
MTRLQPPDWLKRGLRPLRTIRGTISAAFSILILGAVGITSLNSYKLSEEAVLTNSQAYMGEVIQQVGQNIQSYIDNMENISLLIFTNKDVKYYLSDNPFLSREEIRAYEKNISDLFQSLLYTRKDIASIMVFGYNGRNVSDRRLTTLNPYVRLREQDWYVKAARAGGRSVISAPHVQNVVTGDYEWVVSLSRELKNSNGMTGQGIALVDLKLNVINEICRSVKLGARGYVFIVDSAGDIVYHPQQQLLYSKLREEPIERILSAGRSSFLVDDGAGERLYSVQDSNFGWKIVGVAYRSELIADPDAMRNSFLLWAAAALAGTLLISLLLSHRITRPIRRLQAAMRQVERGNFEVRAEVEQVNEIGQLERTFNMMVGQTQRLMDERIQTEETKRRTELRLLQSQINPHFLYNTLDSIIWMAEQRKNEEVVRMTSALAKLFRASIAKDDELVPIRIEQEHIASYLQIQKMRYRDMLDYEIDIPRELHLYKTPRILLQPFVENAIYHGIKNMPEGGVIKIAGELDGDSIRFTVRDNGKGMDEETVRAVLSASARDNDGRDHIGVSNVNERIVLTFGAGYGVSIESEPGEGTCVVVTIPKVR
>NZ_CP045802.1|WP_153783240.1|1978513_1979488_+|substrate-binding-domain-containing-protein
MGSKKLWLPLLLLLFAALVVWIGLKRSQPAAAGGGIAVILQTKDVNSSYWQTVRSGALAAAKELNVALELLGPSGAEAAQEQKELLRKAIAARPDAIVLAPISEERLSEELAACRKAGIKLIVIDTPLLQHPYDSYVSSDHVEEGRVAADMLAPDKRKKPVYAFITSDDDSVVASQRRQGVLERLPPGEAFSLGTIDVGKSEEQAYRTVKSLTVAYPGMNGIVALTDVGVSGAARALEDQGLSHSVKLIGFDSSLPEIQLLERGRMHALIVQNPFNMGYLGVETASALREGRKRPQWVDIPSSTITTANMYEPENQKLLFPFVY
>NZ_CP045802.1|WP_153783241.1|1979312_1980887_+|extracellular-solute-binding-protein
MRLSSRTRSTWAISASRRQAPSGRAGSGRSGWTSRPRRSRRPTCTSRRTRSCCSRLSIDFSLIKEEAPDMMNDRRSEASAPAADPPRPRQAAKARASASAAHRTAARRRQLARTAAALALAALMAGCASSSPAPEVTEPEPHQALIKFVASEYSTETKPLLEDIVKGFESLHPDIRVELQVVNWDILDGVYTNMLAQGEPPDLLNANFYAHFAADGLLNDFRNILPEPFLDNLQPSLLARAEYEGTLAAIPYVASMRSLYYNEELFDQAGIAGPPRTWSQLVEDARLVRAGGHGEGFGIDMTDNEIHSYLSYFFYGAGGGWIKDGRWAIDQPANVEGLELLKSMYDAGLTDADPWLTTRDEKQRVLGSGGLAMMISGNYFSSVVPKEFPGLRWGRGPIPVKDGQPPMTFGVQDVLVSFKTAHSDPAALSAFIQYLYEDERYADMVRQEGFLPTTRSAGALLSEGDAEMRANLDDLAGARFVPIEQPRWSNVMDAARKLGSAVLQGRYSPQSALEELQKIAVKQD
>NZ_CP045802.1|WP_101808886.1|1981159_1982542_+|extracellular-solute-binding-protein
MTFTVKKTAAGAMAIAMSLAVLAGCGGNNGNSGNTGEAANEPATNSATNAAAENTSATGGETKLSGDFTVQYFVGGYGDKWWKQVIADFKAANPDLNIKEEAGPQINTQNKPKWIAGTPPDFVYIDGPELNDRQMAEDGQLEDLTDWLQTATNVDGVKILDLLAQQPPQYGGKTYNVPLVLNSWGIFYNKALFEKNGWTEPKDWDTFISSSEAIKAAGTTPFIHTGKYPYYINSSFLFPAIVSANGNDYKLLQDMGDSKVEAFKSPQVLEALGKIVELRDKGFIDKASVSINHTDSQMLFLQNKDAYIPNGLWLPNEMSKDVPADFKFGFIPSVTQKAGDKVVANTSTSTVAIAKNAKNKEAAKAFLQFIFSESQASKFAELSGAPSNIKGDISSSAAPDFVKQAAAYLTADTTVVVPTVTFNQDVDKAMQDATVALTIGKIDPQGWVDRVVKVVEKVAK
>NZ_CP045802.1|WP_101808887.1|1982649_1983552_+|sugar-ABC-transporter-permease
MRLGGAKGQRKLFIAAFIIPTFLYFCLFTIYPIVQALYNSFYDWSGMSQHKDFVGLQNFKDLLQDPIMLTAIGNDYFLVAGKMIGIMAIATFFAVALTRLRIRGAGFFRSIFFIPNVLSVVVVGILWGFIYNPQIGFLNGFLSLFTKEPVTINWLGFESHSIWMLLPPTIWAGIGFYMILLIAAITNIPESLYEAADIEGAGQWHQFRHITLPLVWEQMKISVINIMMTTLNGSFVIVTIMTAGGPDNSTQVMGSYLYQQAFKQAHFGYGASIGIAILTTSLVTTVFLQWLLRKDQVEVS
>NZ_CP045802.1|WP_153783242.1|1983584_1984430_+|ABC-transporter-permease-subunit
MVQRTVHPVIKGFFMLLLVLWGVSVLYPLLWTLMDSLKDNQQFYFNMPWALPELPLQWSNFGYVWNNYNFGKYFVNSILVTTGATLLGLVLASMTAYTIARYRFIGSRVLYLIYISSMMVPFSLALIPLFFLVNDLGLTNTPLGLIFVYASNTLAFGIFVLIGFFKTLPKELEEAAAIDGAGYFGTFFRVMLPLSRSGLISVGIINVLDIWNEFIVGTILVNDPAKYTLPIGLAAMQVEMQYKTEWGPLFAGLLFTIVPVLIVYMFAQRHIVSGLVAGAVK
>NZ_CP045802.1|WP_127464541.1|1984552_1984846_+|hypothetical-protein
MKGGGRPAGSAAAGQRHTVGLRSDGKVVAGGDNDDGPCEVGGWSGIGLPGSVVSRLLNRRFLLFRGTHALTIRCQRLLRRLESLFPSLPKSNDESDA
>NZ_CP045802.1|WP_101808889.1|1985145_1986465_-|hypothetical-protein
MQTNGIYASSTPSAIAAKNNPLPAKVPVPASSHASHAVETYTPSVIDEGQQGLRALGGQWIVGREFTSVQGTDYSKNFLDDVSGFLVKSAYERDLLLQRYAGDELNQQLEQYDKQVQLKLEDIAQTTASTLSQYLNFENDSIFGGSKETQGEFLSAYKPLFDKNELTDRIKNMLQEQSRILDKLQEEQGDQWKQVMEQGGKEITDFRDLLKEEASKASGGESTSFQDISYRDVAAVFDALVHTTAKAMNTSTFDTEWMANNLGTARLKLELYLQQSPMSSAIKEQLTQSVDKAMSTKMGIAEYEDYKSSLVSTPSFRKQFASHQEMTLEIKRMYSDHLQDPNAKKSVGTIMWESMKELLNQKPEHLLSGLMDSFNRLHHSLISSPSMEGDVGPKAKLEFANQVRDANLEDWNSFISSLNMGQQQKSALTMPKNSIDIKV

Crispr_ID: NZ_CP045802_14

• CRISPR_ID: NZ_CP045802_14
• CRISPR_location: 2481629-2481764
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_14

Consensus_repeat	Method
TCGTTCCAGGCACATCGGAGTCTCGACTGTTCGCTATCCCGTTCGACGGCA	CRISPRCasFinder

spacers of NZ_CP045802_14

>14.1|2481680|34|NZ_CP045802|CRISPRCasFinder
ACACGAGCGATGCGGGGGGATAAGCAGCAGCTGA

CRISPR arrays and Neighbor proteins around NZ_CP045802_14

CRISPR arrays

The CRISPR arrays of NZ_CP045802_14

>merge|NZ_CP045802|14|2481629-2481764|CRISPRCasFinder
TCGTTCCAGGCACATCGGAGTCTCGACTGTTCGCTATCCCGTTCGACGGCAACACGAGCGATGCGGGGGGATAAGCAGCAGCTGATCGTTCCAGGCACATCGGAGTCTCGACTGTTCGCTAACCCGTTCGACGGCA

>NZ_CP045802|14|12|2481629-2481764|CRISPRCasFinder
TCGTTCCAGGCACATCGGAGTCTCGACTGTTCGCTATCCCGTTCGACGGCA	ACACGAGCGATGCGGGGGGATAAGCAGCAGCTGA
TCGTTCCAGGCACATCGGAGTCTCGACTGTTCGCTAACCCGTTCGACGGCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_028599639.1|2494361_2494577_-|spore-gernimation-protein	unknown	unknown	gnl|CDD|313906
NZ_CP045802.1|WP_153783444.1|2486892_2488356_+|glycogen-synthase-GlgA	unknown	unknown	gnl|CDD|234809
NZ_CP045802.1|WP_153783447.1|2494573_2494813_-|spore-gernimation-protein-GerPA	unknown	unknown	gnl|CDD|371190
NZ_CP045802.1|WP_153783445.1|2488337_2490296_+|glycoside-hydrolase-family-15-protein	unknown	unknown	gnl|CDD|225922
NZ_CP045802.1|WP_028599637.1|2490993_2491590_-|spore-germination-protein-GerPE	unknown	unknown	gnl|CDD|287884
NZ_CP045802.1|WP_153783433.1|2468996_2469857_+|hypothetical-protein	unknown	unknown	gnl|CDD|379241
NZ_CP045802.1|WP_153783443.1|2484464_2485631_+|glucose-1-phosphate-adenylyltransferase	unknown	unknown	gnl|CDD|179997
NZ_CP045802.1|WP_153783446.1|2491943_2494337_-|hypothetical-protein	unknown	unknown	gnl|CDD|371215
NZ_CP045802.1|WP_153783436.1|2473357_2473984_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|224584
NZ_CP045802.1|WP_153783437.1|2473880_2474897_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|225117
NZ_CP045802.1|WP_153783441.1|2480820_2481498_+|transcriptional-regulator	unknown	unknown	unknown
NZ_CP045802.1|WP_084137414.1|2490854_2490971_-|sporulation-protein-YjcZ	unknown	unknown	unknown
NZ_CP045802.1|WP_153783435.1|2472046_2473279_-|aminopeptidase	unknown	unknown	gnl|CDD|376723
NZ_CP045802.1|WP_153783438.1|2474987_2476490_+|alpha-galactosidase	unknown	unknown	gnl|CDD|185035
NZ_CP045802.1|WP_153783440.1|2480115_2480601_+|disulfide-bond-formation-protein-B	unknown	unknown	gnl|CDD|179540
NZ_CP045802.1|WP_084137417.1|2479338_2480001_+|thioredoxin-domain-containing-protein	unknown	unknown	gnl|CDD|372611
NZ_CP045802.1|WP_153783439.1|2476755_2479131_+|hypothetical-protein	unknown	unknown	gnl|CDD|223633
NZ_CP045802.1|WP_153783434.1|2469959_2471918_+|response-regulator	unknown	unknown	gnl|CDD|274362
NZ_CP045802.1|WP_153783442.1|2482404_2484447_+|1,4-alpha-glucan-branching-protein-GlgB	unknown	unknown	gnl|CDD|235445
NZ_CP045802.1|WP_101808998.1|2485627_2486740_+|glucose-1-phosphate-adenylyltransferase-subunit-GlgD	unknown	unknown	gnl|CDD|273966

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_028599639.1|2494361_2494577_-|spore-gernimation-protein	gnl|CDD|313906	pfam10803, GerPB, Spore germination GerPB. Members of this family are required for formation of functionally normal spores. They may be involved in the establishment of spore coat structure or permeability.	3.4309e-23
NZ_CP045802.1|WP_153783444.1|2486892_2488356_+|glycogen-synthase-GlgA	gnl|CDD|234809	PRK00654, glgA, glycogen synthase GlgA.	0
NZ_CP045802.1|WP_153783445.1|2488337_2490296_+|glycoside-hydrolase-family-15-protein	gnl|CDD|225922	COG3387, SGA1, Glucoamylase and related glycosyl hydrolases [Carbohydrate transport and metabolism].	9.78464e-109
NZ_CP045802.1|WP_028599637.1|2490993_2491590_-|spore-germination-protein-GerPE	gnl|CDD|287884	pfam10970, GerPE, Spore germination protein GerPE. GerPE is required for the formation of functionally normal spores. It could be involved in the establishment of a normal spore coat structure and (or) permeability, which allows the access of germinants to their receptor.	2.17626e-19
NZ_CP045802.1|WP_153783433.1|2468996_2469857_+|hypothetical-protein	gnl|CDD|379241	pfam13529, Peptidase_C39_2, Peptidase_C39 like family.	2.88894e-09
NZ_CP045802.1|WP_153783443.1|2484464_2485631_+|glucose-1-phosphate-adenylyltransferase	gnl|CDD|179997	PRK05293, glgC, glucose-1-phosphate adenylyltransferase; Provisional.	0
NZ_CP045802.1|WP_153783446.1|2491943_2494337_-|hypothetical-protein	gnl|CDD|371215	pfam10737, GerPC, Spore germination protein GerPC. GerPC is required for the formation of functionally normal spores. The gerP locus encodes a number of proteins which are thought to be involved in the establishment of normal spore coat structure and/or permeability, which allows the access of germinants to their receptor.	9.53001e-22
NZ_CP045802.1|WP_153783436.1|2473357_2473984_+|GNAT-family-N-acetyltransferase	gnl|CDD|224584	COG1670, RimL, Acetyltransferases, including N-acetylases of ribosomal proteins [Translation, ribosomal structure and biogenesis].	2.02017e-27
NZ_CP045802.1|WP_153783437.1|2473880_2474897_+|helix-turn-helix-domain-containing-protein	gnl|CDD|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	3.35588e-26
NZ_CP045802.1|WP_153783447.1|2494573_2494813_-|spore-gernimation-protein-GerPA	gnl|CDD|371190	pfam10676, gerPA, Spore germination protein gerPA/gerPF. This is a bacterial family of proteins that are required for the formation of functionally normal spores. Proteins in this family may be involved in establishing normal coat structure and/or permeability which could control the access of germinants to their receptor.	3.00547e-18
NZ_CP045802.1|WP_153783435.1|2472046_2473279_-|aminopeptidase	gnl|CDD|376723	pfam02073, Peptidase_M29, Thermophilic metalloprotease (M29).	0
NZ_CP045802.1|WP_153783438.1|2474987_2476490_+|alpha-galactosidase	gnl|CDD|185035	PRK15076, PRK15076, alpha-galactosidase; Provisional.	0
NZ_CP045802.1|WP_153783440.1|2480115_2480601_+|disulfide-bond-formation-protein-B	gnl|CDD|179540	PRK03113, PRK03113, putative disulfide oxidoreductase; Provisional.	1.13911e-50
NZ_CP045802.1|WP_084137417.1|2479338_2480001_+|thioredoxin-domain-containing-protein	gnl|CDD|372611	pfam13462, Thioredoxin_4, Thioredoxin.	8.35238e-29
NZ_CP045802.1|WP_153783439.1|2476755_2479131_+|hypothetical-protein	gnl|CDD|223633	COG0559, LivH, Branched-chain amino acid ABC-type transport system, permease components [Amino acid transport and metabolism].	0.00217028
NZ_CP045802.1|WP_153783434.1|2469959_2471918_+|response-regulator	gnl|CDD|274362	TIGR02956, sensor_protein_TorS, TMAO reductase sytem sensor TorS. This protein, TorS, is part of a regulatory system for the torCAD operon that encodes the pterin molybdenum cofactor-containing enzyme trimethylamine-N-oxide (TMAO) reductase (TorA), a cognate chaperone (TorD), and a penta-haem cytochrome (TorC). TorS works together with the inducer-binding protein TorT and the response regulator TorR. TorS contains histidine kinase ATPase (pfam02518), HAMP (pfam00672), phosphoacceptor (pfam00512), and phosphotransfer (pfam01627) domains and a response regulator receiver domain (pfam00072). [Signal transduction, Two-component systems].	2.37053e-85
NZ_CP045802.1|WP_153783442.1|2482404_2484447_+|1,4-alpha-glucan-branching-protein-GlgB	gnl|CDD|235445	PRK05402, PRK05402, 1,4-alpha-glucan branching protein GlgB.	0
NZ_CP045802.1|WP_101808998.1|2485627_2486740_+|glucose-1-phosphate-adenylyltransferase-subunit-GlgD	gnl|CDD|273966	TIGR02092, Glycogen_biosynthesis_protein_GlgD, glucose-1-phosphate adenylyltransferase, GlgD subunit. This family is GlgD, an apparent regulatory protein that appears in an alpha2/beta2 heterotetramer with GlgC (glucose-1-phosphate adenylyltransferase, TIGR02091) in a subset of bacteria that use GlgC for glycogen biosynthesis. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	2.59572e-133

Protein sequences

>NZ_CP045802.1|WP_153783441.1|2480820_2481498_+|transcriptional-regulator
MPNFQTAYDEWLQAEIQDETNPRRRELLEKGLGHGTVAFLKQIWFPTMRSFKHLHPEWEVRDASNGYRYVDLAYLPGGGAKGGIEIQGFGPHARDLDVRRFKDLSWRYSMLSIDDWLFIPVAYLSIVEEPKRCQQLVLSFVGKFIAGESAGSLTALEAETVRYARRVFRPFTPSELTVHLNVSAAYARRILHRLVELGRLKQVGGNLRYRSYALPDWRPLPGSDG
>NZ_CP045802.1|WP_153783440.1|2480115_2480601_+|disulfide-bond-formation-protein-B
MAEQNTEGELPEHDERDSFDEDEPQGLWERYRFYCAWVVALAATLGSLYLSEVAGYMPCDLCWYQRIFMYPLAVLLGIAAYRGDRQIGVYALPLAWIGIAISFYHNLLQWFPSLSGIVPCKSGVPCNQDYLNWLGFITIPLMALTAFALILILLHVKGRRR
>NZ_CP045802.1|WP_084137417.1|2479338_2480001_+|thioredoxin-domain-containing-protein
MPPAKQKKGNGALIWLTIAIAFIAVVIILGINNSSKPHAFNYGEMPRLGDENAQVKLVEFGDYKCPSCKLFSEQVKPLLVQDYINDGKAALYFANYAFLGQDSVTAAVAAHSVYLQDPEQFWAYNDAIYANQGDETTVWATPERLVQIAKDAKLDIDFDKLLSDINAGVGSDKVAEESRLAESTLKVGGTPSLFVDGEQLQFKGYDDIKKAIDAKLDEKK
>NZ_CP045802.1|WP_153783439.1|2476755_2479131_+|hypothetical-protein
MSIEWGPLGRAGQPNRKPWRKRLLPQEAPGQRDTAFWLRSMAGVWIGAAFLCAACAQGLPLGFGPAYDLMAMTLAGTAALGIAAWALSWLLCWMRLPLPRRFAGGALALAAGTAGALLVAELRWTAALPLAAAYSLAAAVGGVAFAAALPRLRLRRPQPLAALLCSAGALLVLPLLLSLPAPGFGGSADDADGAGAAGSAIAPDLPGRSGAYAYSVLTYGSGTGRRAEFAAEADIRTSSADASALLTDWSRLKAWYWGFEPDRFPLNGTMWLPDGDGPFPLALIVHGNHIAQQRSDAGYAYLGERLASKGYAAVSVDENFLNFSPWTGIPDDDMKLRAWLLLRHLEELKRLSGQPDGPLAGKLDASRTLLIGHSRGGQAAAMAADAGKWFPGDAALARSVLGVAALAPTDTEEDGQRAVLEHASYLTLHGSRDADLTVFYGERQYGRVRLDPGSDRFKAAVYIEDANHSRFNADWGTMDNSLPGGLLLRQRDMLSGERQRLLAASYVGAFADAVLGGDAAARAWLLPESDAAAAWPEEQGVSGEAEAGRPEAVSGVRTYRLYADADELPVADFEQEDARQAGSGVRAEAADGSSLSAEPLLDRNGSPKGSRGAVVSWGALGAAAERPGSDEDAAGSSAASEGSWLRLTGLPQPPDPGGGGISFTAANLGRELCSEGAGCEPQALQLQVVLRDRNGAEAEVAVADALAAVEDEPFLRPAWLDGFASEGKYDRPAELARVTIRLPLSAFREAEPLLDTDSLDRLELRFRSADGGAGRIMLDDVSWYAGETAGR
>NZ_CP045802.1|WP_153783438.1|2474987_2476490_+|alpha-galactosidase
MSFKVAFIGAGSIGFTRGLLRDLLSVPEFAGIEVAFADIDPDNLERVRSLCQRDIDENGLAIRIQATTDRREALKGAKYILNTIRVGGLEAFRTDVEIPLRYGIDQCVGDTLCAGGIMYGQRGIAEMLAICKDIREFAREDALLLNYANPMAMLTWACNAYGGVRTIGLCHGVQGGHHQIAQALGLEMDEVDIVCAGINHQTWYVSVKTGGVDRTGDLLEAFERHPDFARTEKVRIDMLRRFGYYSTESNGHLSEYVPWYRKRPQEIPDWIDLNSWINGETGGYLRVCTEGRLWFETEFPAWMKEPALRYEASERSQEHGGYIIESLETGRVYRGHFNVVNRGVISNLPDDCIIEAPGYVDRNGISMPVVGDLPLGPAAVCQASVNVQRLAVEAAVRGDDKLLRQAFLMDPLVGAVCNPPEVWQLVDEMLVAGERWLPQYGEAIAAAKERLAAGNLIPTREYEGAARLQTKTLEQMQAARDEADANAREADKGKRRAEQR
>NZ_CP045802.1|WP_153783437.1|2473880_2474897_+|helix-turn-helix-domain-containing-protein
MRTACSSTMPSTACWRETGREGGRAPMFRTGSLFDPAVRRGGCEPEVTAYYFKKWQGYAMDYHRHDATEIMYVMEGGCLVETEPGTPMEPGSAASRLKRGDLVLLDANVPHRLLVREECRMLNVEFRFVAAAAPLAEAAALAEADAPLAEWLSRKAPSLVLRDSRERALQTLRQLVLELDESGIGGSAMSRLLHAQLLLRLSRLETAHAAERPQDGYVEQAKRYMAERLDQPLQAEQVAAAVRLHPGYLQRIFRQAEGVTLGGYLSAIRLEKARQLLRHSSIPVSDLWDYVGLGSRAYFHAWFRRQTGMTPSEFRRSVTADSRPDSAYSPGQGSDFEQ
>NZ_CP045802.1|WP_153783436.1|2473357_2473984_+|GNAT-family-N-acetyltransferase
MMEKTSPLSGREAKAMFHRRLEGGCELRVLAPADAKALYRTLEKDRRELETWLPWVGQIRSAADMKDYVRFECKRYKEGKAMSAVLLDGASAAGMISFQELDFRHRKASLGYWLGSAWQGRGLMAQAAGEMLSFAYGTLDLNRVEIRARTDNRRSRAVALRLGFSLEGVLREEEHADGMFLDHAVYGLLARDWARGRASTDVPDRQPV
>NZ_CP045802.1|WP_153783435.1|2472046_2473279_-|aminopeptidase
MSKLQQQIERYADLIIRVGVRIQPGQKLAINATLDSADLVRGLVRKAYEAGAYSVKVNWSDDTIARTRYELAPDEAFLEEPKWYAGEMTELGEQGGAAISVVSSDPDLLKGIDKQRIVNHQKTYGKAMAAYRQMTQSDKFSWCVVAAPSKAWAAKVFPGSTEEEQYISLWNSILKAVRCDLDDPVAAWEEHIASLNSRSEHLNARKYKKLHYTAPGTDLMIELPEGHLWVAADSVNEAGIPFVANLPTEEVFTAAKADGVNGYVSSTKPLSYGGTIIDNFKLTFENGSVVKAEAERGLETLEGLLEMDAGARRIGEVALVPFDSPISRSNILYYNTLFDENASNHLALGSAYAFNIEGGKGLSQEELAARGLNTSITHVDFMIGSADMNIDGIAEDGSVEPIFRAGNWAF
>NZ_CP045802.1|WP_153783434.1|2469959_2471918_+|response-regulator
MENNAAQRSGAGGRTPAQPSRAMLASVISLSPVPLLLFDSGLSIMTVNPAFLRTFACTEQELTGLGADALARLCFPADSLCRAELARIRQLEPIDCEEEMTLQSGERRMFRIIGYALDGEEGAGGGYLLSLEDVSERKRFELQLQESVERYTSLKKYNHDAVISLDLQGRVINYNQEAGRLLGMPVEELAGKDFSPYLLVEEIGPILRQASQDTEAERQLSGMRHRSGRVTEILASIAPIIINGTIKGYYLIAKDMSEQKKLLIEKEAAEATNRAKNEFLTMMSHEIRNPMNGILGLTRMVLDTPLEEEARRYIELIRKSSHALLHIVNDTLDYTRLESAGAEAAEERPFRLAELLDEIVAIQMPIVVQKGLKLETAIAADVPAELLGDREKLGKVLLNLIGNAVKFTERGQIRAVFSAGGEDRGSRLIECEVSDTGIGITETEQQQLFHPFRRIGTYMTRTEEGSGLGLAISRRLVELMGGTIEVESEPGQGSRFRFAAKAARDQPPHALPDAAMAAPEPDGPLRVLVAEDNEINQLVIRKMLEKSGHSVRVVANGAEVLEALQEPEPYDLLLLDILMPVLGGFETMDEIRAMGLARPPYVVAVTANALRGDREACLAAGMDDYLSKPIRRDKLEEAIDAYRSSAKARQRG
>NZ_CP045802.1|WP_153783433.1|2468996_2469857_+|hypothetical-protein
MSGATASGSTPEFRGPLSAASAAAPNAAVRLVQERLSALGYSGADGAPLKADGCFGRNTLHAVNRFKTRSRLGNAGSAAGVVGRQTWEALFASTAVREERVSRERIYYSQEDPRWRNVPYTIGGKETIGSSGCGPTCMAMAVASLTQARPLPTELAAFSVKGGHRTRASGTSWSFFPAASREYGLACKATGSIDEARAALQRGDVAIASMKPGRFTSAGHFILLAEPARTAAGEPGFLVFDPNPDNRLYRGAVDEGVPDDGRVTAPEALLRQEAKQFWLLAAGPAG
>NZ_CP045802.1|WP_153783442.1|2482404_2484447_+|1,4-alpha-glucan-branching-protein-GlgB
MPTLKPKQPVPSDPAVLDGRPASIDQPADSKPSAKPRASAKPKPSAKSKQDKALLKDVYLFNRGENDFAYRTFGAHVKLEERRRGVRFTVWAPNAREVGVAGDFNGWDGVQHRMEPVDATGVWSLFIPGLKAGDLYKYEIVTADGRKLLKADPFAFASELRPNTASVVADLSGYKWKDDEWERRKRTTSPYDQPMLVYEMHLGTWKIKAPEVFYSYDEIGGEIIDYVVRMGYTHIELMPLAEHPLDKSWGYQITGYFAPTARYGPAKSLMKFIDRCHRKGIGVILDWVPAHFVKDEQGLRRFDGTPLYESADPSLAEKPLWGTNAFDYGRTEVQSFLISNALYWMDLFHVDGLRVDAVASMRDLTMDKPPELQARNIYGGTRHLEADAFLQKLNKAVFRYFPNTLMIAEDSSPEPGVTAPVHDGGLGFNFKWSMGWMNDMLRYMQLDPSQRSQRHDWLTFAMMYHHTENFILPLSHDEVVHGKKSLLNKMPGSYEEKFANLRLFYGFWMAHPGKKLLFMGGEFGQFDEWKDSESLDWMVLEYDSHRSMQQYVRKLNGLYRKLPQLWEQDYDPAGFEWIDADNAEQSVVSFIRRSKDGGYAVAVANFSRSSYEDYRIGVPDKGRYKLLLHSDDARLGGASTGLPTSISSQKAPMHGRDYSLTLHLPPLSFQLLEHQPRGTH
>NZ_CP045802.1|WP_153783443.1|2484464_2485631_+|glucose-1-phosphate-adenylyltransferase
MGQKEMIAMLLAGGEGKRLGVLTKDLAKPAVHFGGKYRIIDFTLSNCMHSGIDTVGVLTQYQPLVLNRYLGIGSPWGLDRSDGGMAVLPPYVKSKGGDWYKGTANAIYQNMGFIDRYEPEYVLIISGDHIYKMDYEKMLEHHKSTGADVTVAGLEVDIKEASRFGTMILGEGFRIVDFEEKPKHPVSNVVSMGVYIFSWKVLQKYLIRDEADRKSSHDFGKDIIPAMLEDDIHLHMYPFKGYWKDVGTIESLWEAHMDLLGCEPQLDLGDSDWRIYSTRHNRPAHYVSPAASIRESMITEGCVVEGEVSRSVVFSGVEIGEGSLISESVIMPGAVIGAGCKVYRTIIGENAVLEPGVMLGSPDGTEIGVVGSDEKIGRNHSLQEVQQP
>NZ_CP045802.1|WP_101808998.1|2485627_2486740_+|glucose-1-phosphate-adenylyltransferase-subunit-GlgD
MINKAMGVVNLIHETDELESLTATRCPATVPFGARYRLIDFILSSMVNSGISKVAVFAHTKYRSLMDHLGSGRPWDLHTRQSGLFVLPPSSDQIHELSRGDLYHFYQHRDYFQRCKLEYVVVTRSHMVCNVDLDAVIDYHESQNADITVICKKQADLLGGKTRKVELGEGGRVKDMQDHFGNMDSDVHSMEIYVMKKDLLMDLVQTSLAQGQDHLVRHAILSRIDRLRIFGYLYEGYLGVVNTVEAYYRTSMDLLRPEAWRELFFRPGPIFTKTKDEPPTRYLEGAKTGNSLIANGCKIEGTVINSVLFRGVHVGKGAVIRNSIVMQNGVIGDGTQLDRVILDKESQVEPHRDIRGTAGLPFVAGKRKTI
>NZ_CP045802.1|WP_153783444.1|2486892_2488356_+|glycogen-synthase-GlgA
MNVLFATSEAVPLAKTGGLADVAGALPKALRQAGTEARVILPKYDTIPWTLAQRFRKIDEFTVQLGWRTQYCGLLEGEVDGVVYYLIDNEFYFHRGGLYGYGDDPERFVFFSIAVLEAARRMDIRWDVLHCHDWQTGLIPFLLKRRYFADERLSSVRTVFTIHNLRYQGVFGKQEMMDLIGMGPEIFAWDGLEHDGAANCMKGGLLYADKLTTVSPTYAEEIKTEYYGEGLDGILRMRAGDLAGIVNGIDTELFDPMNDEAIAVPYLDSLERKRQNKLALQKELGLPQREDVPVIGIVSRLVEQKGFDLIDGVFGELLEEDMQLAVLGSGEWKYEEMFRSASHTRYDKVSLATGFNDGLARRIYAGSDLYLMPSQFEPCGLSQLLALRYRSVPIVRETGGLKDTVQPYDEYTGRGNGFSFASYNAHDMLFTIRRALHFYREPAAWEAIVRNGAGDDYSWNRSARSYIDLYEQLAPERKEKDSWPVTS
>NZ_CP045802.1|WP_153783445.1|2488337_2490296_+|glycoside-hydrolase-family-15-protein
MARHLVIGNGKMLLNLDQNCYIRDIYYPYVGQLNHVGGQYCRLGLWTEGQFSWLEDPAWSRELGYIEDSLVTDVTARHGGLGVELQMNDGIHQRECIYLKRVVIRNHADREREFRLFFHQDLMIDGTEVGDTAAYYPDNHTLFHYKRSSYFMFNGFSDEGGMSQYSTGIKRFHSAEGTWRDAEDGVLMGNAIAQGSVDSTISFRTVVPAGGEKTVYYWMSIGKSLEEVKQLNDYVQDQHPEKLLSRIVVYWNHWLGRAEKDLGDLPPEVARMFRQSLLLVRTQTDERGAIIAANDTDILQYNRDHYSYMWPRDGALVADAMSLAGYQSVIAPFFQFCSEALTPDGYLNHKFNPDGTVGSSWHPYTVQGAKRLPIQEDETALVLFALWRDFQRHQVIELPQSLYSNLIRKSAAFLSSYMEHSLSLPKPSYDLWEERYGIWTYTAASVYGGLMAASFFTDLFGDYERSDHYKRTAEEVKHGILTQLWDEASGRFARGLVQKDGGWVKDMTLESSLFAVLEFGVLPADDERVVRTMTAIRDGLAVRTDVGGIARYTNDYYFQQSGEIDRVPGNPWIICTLWVANFEIDSARCLADLEAPKRTLEWVVRTALESGVLPEQLNPHDGTPLSVAPLTWSHATFVQSVSKYAAKYKELS
>NZ_CP045802.1|WP_084137414.1|2490854_2490971_-|sporulation-protein-YjcZ
MGYAAEGVGAGYGGLGTSTGVILVLFILLVIISRAFFI
>NZ_CP045802.1|WP_028599637.1|2490993_2491590_-|spore-germination-protein-GerPE
MIDSDASIRTSYIGSAELISIGLSSVVQFGDTGSVNARVTGLAVQRQLDHRAGGEVDFAGYSLFVKPFNPIEEESLEEADVRTIRSNPCPAIQVGCVNVIAYSSASVLLGGNAVEVNLESRLKHFRQYAYAITASTEPTPAATELIESAEPAGSGEPLRPILSADPGQLPGSVSPPAAYSEDVKSGNPHGRPFADFAP
>NZ_CP045802.1|WP_153783446.1|2491943_2494337_-|hypothetical-protein
MDPKDSSASGGSSPSGAPEAPPNRSFLSNPLLGMLTGTGGMGGMGSGIVPKLLGKSMAWPGLGGAFPGMMGGKGGGAGWPPPYPGAAAGPGAWPPYPGGGVPGSWGAPAPSPGFPGAWGGGFPGGGAPQAGNWIAPQGAPQPGNWNVPQGAPQAGNWIAPQGATQAGNWIAPQGATQAGNWIAPPGGPQAGGWIAPPGGPQAGGWIAPPGAPQPGNWAAAPQAGWPPSAAPPPAAPPDPSLSPAPGITAATPASPAIEGDNTFQIPGATVVPEPGGSEASSGSWLQPPGQTSFAPPFVPPPAPIPPPAGPQAAPPGSAAGGAAPAGFPPGAFPAGIGIPGIDPNFAPGLNEEAIPKAIASIDPNWVQKWQHYQGWPFSAPPFPFVPDQASEAAAEQAAAEYPCAGNLLDPICLQRCLQALAAGWTAQQRLNEHLTSSMKRIESRLAELETRPSYTIEKLEYNFDQLKVEQLDGTLNIGMTAPSEAQMQEFGQMALPSQVKGGAKVYPLPIPQSAAPGIAQQLAAQAAHSGTGSGIASTPAGSQGPGAPAGAWTPGPEQPSFGNAPGTALAPNLVGSQAPGVLPPQAGGQTLAPGAAAPPGFSGPPGAPNAGAAGTSGIAPPGGPNAPGLIPGSAGFGVPGAQSGLQPGPGAFTAPALDNFSGQPPAGSAAVPPAGAAPAPQPGALPGFTDVRSVVHQWLSESAHDKLESAARGHRLELDPSHRQMVIEDVRRQLPDRIRLYLNEELSSRSAMQAAAGSPLRREQLQRTAQRAIRDAETALEQYAAQLARIAPQRRKD
>NZ_CP045802.1|WP_028599639.1|2494361_2494577_-|spore-gernimation-protein
MNLTVHQSITIHQLRVDSVANSSVLQIGSAGSIRPVSQLYNSGGFDKPAEALTAAEESSNALNFVPLPNPS
>NZ_CP045802.1|WP_153783447.1|2494573_2494813_-|spore-gernimation-protein-GerPA
MPAAVGFVNIVSIGSSGVVQFGDTVQISPSSTSKTYAGSGSFLTGGLTNANNGLSATNTLDPDLQDNSSNQVASGANII

Crispr_ID: NZ_CP045802_15

• CRISPR_ID: NZ_CP045802_15
• CRISPR_location: 2512389-2514408
• CRISPR_type: Orphan
• Repeat_type: NA:I-C
• Spacer_info: 30 spacers

Consensus repeat of NZ_CP045802_15

Consensus_repeat	Method
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	CRISPRCasFinder
GTCGCTCCCCGNNGGGGAGCGTGGATTGAAAC	CRT
GTTTCAATCCACGCTCCCC	PILER-CR

spacers of NZ_CP045802_15

>15.1|2512421|33|NZ_CP045802|CRISPRCasFinder,CRT
ACCCTTTCTCGCTGTTCGGCGGAAGGCCCGACG
>15.2|2512486|35|NZ_CP045802|CRISPRCasFinder,CRT
GTTCGTGTTTAAGAGTCAAAATAGCTTCAGCTGCT
>15.3|2512553|34|NZ_CP045802|CRISPRCasFinder,CRT
CCCAGGCGAGGCCCTATTCGGAAGTACGGTCGAG
>15.4|2512619|34|NZ_CP045802|CRISPRCasFinder,CRT
TTTTCCCGCCTTGGCGAGGATCGCCATATAGTCG
>15.5|2512685|33|NZ_CP045802|CRISPRCasFinder,CRT
GCCGGCGGGGTTGGAAAGGCGTGAACCATGCTG
>15.6|2512750|36|NZ_CP045802|CRISPRCasFinder,CRT
ACCTTGTCCAACTGGCACCGGCGCGGGCGCGACGTC
>15.7|2512818|35|NZ_CP045802|CRISPRCasFinder,CRT
CTCGAATCGAAGGGCTTCACGGTGGTTCGTCACTA
>15.8|2512885|34|NZ_CP045802|CRISPRCasFinder,CRT
GCTCGTTCGGCACGGTCATTCGCGACGTGCTGGA
>15.9|2512951|34|NZ_CP045802|CRISPRCasFinder,CRT
AATAAGACGCATGAGTTGCCGGTAGACCATCGAC
>15.10|2513017|34|NZ_CP045802|CRISPRCasFinder,CRT
CAATTCTTTAATAATGGCTTGAATTGCTTTTTCT
>15.11|2513083|34|NZ_CP045802|CRISPRCasFinder,CRT
CCATATATCGGCATATCCACAATGCGCTACTTTA
>15.12|2513149|33|NZ_CP045802|CRISPRCasFinder,CRT
CATTGCCGCTGGATCGACTCCCGCGCCTCCTGC
>15.13|2513214|33|NZ_CP045802|CRISPRCasFinder,CRT
TCATATATGCAAATGATGGAAGCTGTGCATGCA
>15.14|2513279|35|NZ_CP045802|CRISPRCasFinder,CRT
GCAAAAGCCGCAATCGTATGAAGCCTGCGAACGTC
>15.15|2513346|35|NZ_CP045802|CRISPRCasFinder,CRT
CATTCGCAGATACCGATAATTCTCATTCTCGACTC
>15.16|2513413|34|NZ_CP045802|CRISPRCasFinder,CRT
CGCAGCGGGAAATTGGCAAAGACCTGCGATCCGT
>15.17|2513479|32|NZ_CP045802|CRISPRCasFinder,CRT
ACCGAGCCAGAGCCGCGAAAAGGAGAAGAGGG
>15.18|2513543|34|NZ_CP045802|CRISPRCasFinder,CRT
TGCTACTTGCCGGCCATCGTCGACTGGCCGTTAT
>15.19|2513609|34|NZ_CP045802|CRISPRCasFinder,CRT
TGGAGGACGCCTGCGATTTTCCCGAGGTCTTGGA
>15.20|2513675|35|NZ_CP045802|CRISPRCasFinder,CRT
CTGATCTGGGCGATCAACTGGGTGGTGCGTCGTAT
>15.21|2513742|35|NZ_CP045802|CRISPRCasFinder,CRT
ACGGACACACCCAGCGCCTGCAGCACGTCCGCGAC
>15.22|2513809|34|NZ_CP045802|CRISPRCasFinder,CRT
ACCCCTTGACTACCACTACCACGACGCAAAAAGC
>15.23|2513875|34|NZ_CP045802|CRISPRCasFinder,CRT
GGAAGCTAACATATCACCGAACACCCGTTCGTGA
>15.24|2513941|33|NZ_CP045802|CRISPRCasFinder,CRT
GACTGACGCACGGCCTGCGGACGTTCGCGGAAC
>15.25|2514006|33|NZ_CP045802|CRISPRCasFinder,CRT
TCTCCACAAAAGCCTCTATCATAATAAACAAGG
>15.26|2514071|37|NZ_CP045802|CRISPRCasFinder,CRT
GCCGCCTGGCGAGACGCGACGCCGATGCACAACGATC
>15.27|2514140|34|NZ_CP045802|CRISPRCasFinder,CRT
GTCTGGTTCTTTATATGAGACAACGTCTCAAGAT
>15.28|2514206|37|NZ_CP045802|CRISPRCasFinder,CRT
TGGCCGCCATGCTCGTCTTGTTCGGGCGGGGGTGACG
>15.29|2514275|37|NZ_CP045802|CRISPRCasFinder,CRT
TCAGCAAAGAGTCGTGCATTTTGGAAATGAAGCAGAT
>15.30|2514344|33|NZ_CP045802|CRISPRCasFinder,CRT
TCCACGGCCTCGAGATCCAACGGGATACCGGCC
>15.31|2512421|46|NZ_CP045802|PILER-CR
ACCCTTTCTCGCTGTTCGGCGGAAGGCCCGACGGTCGCTCCCCGTG
>15.32|2512486|48|NZ_CP045802|PILER-CR
GTTCGTGTTTAAGAGTCAAAATAGCTTCAGCTGCTGTCGCTCCCCGTG
>15.33|2512553|47|NZ_CP045802|PILER-CR
CCCAGGCGAGGCCCTATTCGGAAGTACGGTCGAGGTCGCTCCCCGTG
>15.34|2512619|47|NZ_CP045802|PILER-CR
TTTTCCCGCCTTGGCGAGGATCGCCATATAGTCGGTCGCTCCCCGTG
>15.35|2512685|46|NZ_CP045802|PILER-CR
GCCGGCGGGGTTGGAAAGGCGTGAACCATGCTGGTCGCTCCCCGTG
>15.36|2512750|49|NZ_CP045802|PILER-CR
ACCTTGTCCAACTGGCACCGGCGCGGGCGCGACGTCGTCGCTCCCCGTG
>15.37|2512818|48|NZ_CP045802|PILER-CR
CTCGAATCGAAGGGCTTCACGGTGGTTCGTCACTAGTCGCTCCCCGTG
>15.38|2512885|47|NZ_CP045802|PILER-CR
GCTCGTTCGGCACGGTCATTCGCGACGTGCTGGAGTCGCTCCCCGTG
>15.39|2512951|47|NZ_CP045802|PILER-CR
AATAAGACGCATGAGTTGCCGGTAGACCATCGACGTCGCTCCCCGTG
>15.40|2513017|47|NZ_CP045802|PILER-CR
CAATTCTTTAATAATGGCTTGAATTGCTTTTTCTGTCGCTCCCCGTG
>15.41|2513083|47|NZ_CP045802|PILER-CR
CCATATATCGGCATATCCACAATGCGCTACTTTAGTCGCTCCCCGTG
>15.42|2513149|46|NZ_CP045802|PILER-CR
CATTGCCGCTGGATCGACTCCCGCGCCTCCTGCGTCGCTCCCCGTG
>15.43|2513214|46|NZ_CP045802|PILER-CR
TCATATATGCAAATGATGGAAGCTGTGCATGCAGTCGCTCCCCGCA
>15.44|2513279|48|NZ_CP045802|PILER-CR
GCAAAAGCCGCAATCGTATGAAGCCTGCGAACGTCGTCGCTCCCCGCA
>15.45|2513346|48|NZ_CP045802|PILER-CR
CATTCGCAGATACCGATAATTCTCATTCTCGACTCGTCGCTCCCCGCA
>15.46|2513413|47|NZ_CP045802|PILER-CR
CGCAGCGGGAAATTGGCAAAGACCTGCGATCCGTGTCGCTCCCCGCA
>15.47|2513479|45|NZ_CP045802|PILER-CR
ACCGAGCCAGAGCCGCGAAAAGGAGAAGAGGGCGTCGCTCCCGCA
>15.48|2513543|47|NZ_CP045802|PILER-CR
TGCTACTTGCCGGCCATCGTCGACTGGCCGTTATGTCGCTCCCCGCA
>15.49|2513609|47|NZ_CP045802|PILER-CR
TGGAGGACGCCTGCGATTTTCCCGAGGTCTTGGAGTCGCTCCCCGCA
>15.50|2513675|48|NZ_CP045802|PILER-CR
CTGATCTGGGCGATCAACTGGGTGGTGCGTCGTATGTCGCTCCCCGCA
>15.51|2513742|48|NZ_CP045802|PILER-CR
ACGGACACACCCAGCGCCTGCAGCACGTCCGCGACGTCGCTCCCCGCA
>15.52|2513809|47|NZ_CP045802|PILER-CR
ACCCCTTGACTACCACTACCACGACGCAAAAAGCGTCGCTCCCCGTG
>15.53|2513875|47|NZ_CP045802|PILER-CR
GGAAGCTAACATATCACCGAACACCCGTTCGTGAGTCGCTCCCCGTG
>15.54|2513941|46|NZ_CP045802|PILER-CR
GACTGACGCACGGCCTGCGGACGTTCGCGGAACGTCGCTCCCCGTG
>15.55|2514006|46|NZ_CP045802|PILER-CR
TCTCCACAAAAGCCTCTATCATAATAAACAAGGGTCGCTCCCCGTG
>15.56|2514071|50|NZ_CP045802|PILER-CR
GCCGCCTGGCGAGACGCGACGCCGATGCACAACGATCGTCGCTTCCCGTG
>15.57|2514140|47|NZ_CP045802|PILER-CR
GTCTGGTTCTTTATATGAGACAACGTCTCAAGATGTCGCTCCCCGTG
>15.58|2514206|50|NZ_CP045802|PILER-CR
TGGCCGCCATGCTCGTCTTGTTCGGGCGGGGGTGACGGTCGCTCCCCGTG
>15.59|2514275|50|NZ_CP045802|PILER-CR
TCAGCAAAGAGTCGTGCATTTTGGAAATGAAGCAGATGTCGCTCCCCGCA

CRISPR arrays and Neighbor proteins around NZ_CP045802_15

CRISPR arrays

The CRISPR arrays of NZ_CP045802_15

>merge|NZ_CP045802|15|2512389-2514408|CRISPRCasFinder,CRT,PILER-CR
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAACACCCTTTCTCGCTGTTCGGCGGAAGGCCCGACGGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACGTTCGTGTTTAAGAGTCAAAATAGCTTCAGCTGCTGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACCCCAGGCGAGGCCCTATTCGGAAGTACGGTCGAGGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACTTTTCCCGCCTTGGCGAGGATCGCCATATAGTCGGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACGCCGGCGGGGTTGGAAAGGCGTGAACCATGCTGGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACACCTTGTCCAACTGGCACCGGCGCGGGCGCGACGTCGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACCTCGAATCGAAGGGCTTCACGGTGGTTCGTCACTAGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACGCTCGTTCGGCACGGTCATTCGCGACGTGCTGGAGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACAATAAGACGCATGAGTTGCCGGTAGACCATCGACGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACCAATTCTTTAATAATGGCTTGAATTGCTTTTTCTGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACCCATATATCGGCATATCCACAATGCGCTACTTTAGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACCATTGCCGCTGGATCGACTCCCGCGCCTCCTGCGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACTCATATATGCAAATGATGGAAGCTGTGCATGCAGTCGCTCCCCGCAGGGGAGCGTGGATTGAAACGCAAAAGCCGCAATCGTATGAAGCCTGCGAACGTCGTCGCTCCCCGCAGGGGAGAGTGGATTGAAACCATTCGCAGATACCGATAATTCTCATTCTCGACTCGTCGCTCCCCGCAGGGGAGCGTGGATTGAAACCGCAGCGGGAAATTGGCAAAGACCTGCGATCCGTGTCGCTCCCCGCAGGGGAGCGTGGATTGAAACACCGAGCCAGAGCCGCGAAAAGGAGAAGAGGGCGTCGCTCCCGCAGGGGAGCGTGGATTGAAACTGCTACTTGCCGGCCATCGTCGACTGGCCGTTATGTCGCTCCCCGCAGGGGAGCGTGGATTGAAACTGGAGGACGCCTGCGATTTTCCCGAGGTCTTGGAGTCGCTCCCCGCAGGGGAGCGTGGATTGAAACCTGATCTGGGCGATCAACTGGGTGGTGCGTCGTATGTCGCTCCCCGCAGGGGAGCGTGGATTGAAACACGGACACACCCAGCGCCTGCAGCACGTCCGCGACGTCGCTCCCCGCAGGGGAGCGTAGATTGAAACACCCCTTGACTACCACTACCACGACGCAAAAAGCGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACGGAAGCTAACATATCACCGAACACCCGTTCGTGAGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACGACTGACGCACGGCCTGCGGACGTTCGCGGAACGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACTCTCCACAAAAGCCTCTATCATAATAAACAAGGGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACGCCGCCTGGCGAGACGCGACGCCGATGCACAACGATCGTCGCTTCCCGTGGGGGAGCGTGAATTGAAACGTCTGGTTCTTTATATGAGACAACGTCTCAAGATGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACTGGCCGCCATGCTCGTCTTGTTCGGGCGGGGGTGACGGTCGCTCCCCGTGGGGGAGCGTGGATTGAAACTCAGCAAAGAGTCGTGCATTTTGGAAATGAAGCAGATGTCGCTCCCCGCAGGGGAGCGTGGATTGAAACTCCACGGCCTCGAGATCCAACGGGATACCGGCCGTCGTTCCCCGCCGGGGAGCATGATTTGAAAC

>NZ_CP045802|15|13|2512389-2514408|CRISPRCasFinder
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	ACCCTTTCTCGCTGTTCGGCGGAAGGCCCGACG
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	GTTCGTGTTTAAGAGTCAAAATAGCTTCAGCTGCT
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	CCCAGGCGAGGCCCTATTCGGAAGTACGGTCGAG
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	TTTTCCCGCCTTGGCGAGGATCGCCATATAGTCG
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	GCCGGCGGGGTTGGAAAGGCGTGAACCATGCTG
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	ACCTTGTCCAACTGGCACCGGCGCGGGCGCGACGTC
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	CTCGAATCGAAGGGCTTCACGGTGGTTCGTCACTA
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	GCTCGTTCGGCACGGTCATTCGCGACGTGCTGGA
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	AATAAGACGCATGAGTTGCCGGTAGACCATCGAC
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	CAATTCTTTAATAATGGCTTGAATTGCTTTTTCT
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	CCATATATCGGCATATCCACAATGCGCTACTTTA
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	CATTGCCGCTGGATCGACTCCCGCGCCTCCTGC
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	TCATATATGCAAATGATGGAAGCTGTGCATGCA
GTCGCTCCCCGCAGGGGAGCGTGGATTGAAAC	GCAAAAGCCGCAATCGTATGAAGCCTGCGAACGTC
GTCGCTCCCCGCAGGGGAGAGTGGATTGAAAC	CATTCGCAGATACCGATAATTCTCATTCTCGACTC
GTCGCTCCCCGCAGGGGAGCGTGGATTGAAAC	CGCAGCGGGAAATTGGCAAAGACCTGCGATCCGT
GTCGCTCCCCGCAGGGGAGCGTGGATTGAAAC	ACCGAGCCAGAGCCGCGAAAAGGAGAAGAGGG
CGTCGCTCCCGCAGGGGAGCGTGGATTGAAAC	TGCTACTTGCCGGCCATCGTCGACTGGCCGTTAT
GTCGCTCCCCGCAGGGGAGCGTGGATTGAAAC	TGGAGGACGCCTGCGATTTTCCCGAGGTCTTGGA
GTCGCTCCCCGCAGGGGAGCGTGGATTGAAAC	CTGATCTGGGCGATCAACTGGGTGGTGCGTCGTAT
GTCGCTCCCCGCAGGGGAGCGTGGATTGAAAC	ACGGACACACCCAGCGCCTGCAGCACGTCCGCGAC
GTCGCTCCCCGCAGGGGAGCGTAGATTGAAAC	ACCCCTTGACTACCACTACCACGACGCAAAAAGC
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	GGAAGCTAACATATCACCGAACACCCGTTCGTGA
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	GACTGACGCACGGCCTGCGGACGTTCGCGGAAC
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	TCTCCACAAAAGCCTCTATCATAATAAACAAGG
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	GCCGCCTGGCGAGACGCGACGCCGATGCACAACGATC
GTCGCTTCCCGTGGGGGAGCGTGAATTGAAAC	GTCTGGTTCTTTATATGAGACAACGTCTCAAGAT
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	TGGCCGCCATGCTCGTCTTGTTCGGGCGGGGGTGACG
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	TCAGCAAAGAGTCGTGCATTTTGGAAATGAAGCAGAT
GTCGCTCCCCGCAGGGGAGCGTGGATTGAAAC	TCCACGGCCTCGAGATCCAACGGGATACCGGCC
GTCGTTCCCCGCCGGGGAGCATGATTTGAAAC

>NZ_CP045802|15|3|2512389-2514408|CRT
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	ACCCTTTCTCGCTGTTCGGCGGAAGGCCCGACG
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	GTTCGTGTTTAAGAGTCAAAATAGCTTCAGCTGCT
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	CCCAGGCGAGGCCCTATTCGGAAGTACGGTCGAG
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	TTTTCCCGCCTTGGCGAGGATCGCCATATAGTCG
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	GCCGGCGGGGTTGGAAAGGCGTGAACCATGCTG
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	ACCTTGTCCAACTGGCACCGGCGCGGGCGCGACGTC
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	CTCGAATCGAAGGGCTTCACGGTGGTTCGTCACTA
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	GCTCGTTCGGCACGGTCATTCGCGACGTGCTGGA
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	AATAAGACGCATGAGTTGCCGGTAGACCATCGAC
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	CAATTCTTTAATAATGGCTTGAATTGCTTTTTCT
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	CCATATATCGGCATATCCACAATGCGCTACTTTA
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	CATTGCCGCTGGATCGACTCCCGCGCCTCCTGC
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	TCATATATGCAAATGATGGAAGCTGTGCATGCA
GTCGCTCCCCGCAGGGGAGCGTGGATTGAAAC	GCAAAAGCCGCAATCGTATGAAGCCTGCGAACGTC
GTCGCTCCCCGCAGGGGAGAGTGGATTGAAAC	CATTCGCAGATACCGATAATTCTCATTCTCGACTC
GTCGCTCCCCGCAGGGGAGCGTGGATTGAAAC	CGCAGCGGGAAATTGGCAAAGACCTGCGATCCGT
GTCGCTCCCCGCAGGGGAGCGTGGATTGAAAC	ACCGAGCCAGAGCCGCGAAAAGGAGAAGAGGG
CGTCGCTCCCGCAGGGGAGCGTGGATTGAAAC	TGCTACTTGCCGGCCATCGTCGACTGGCCGTTAT
GTCGCTCCCCGCAGGGGAGCGTGGATTGAAAC	TGGAGGACGCCTGCGATTTTCCCGAGGTCTTGGA
GTCGCTCCCCGCAGGGGAGCGTGGATTGAAAC	CTGATCTGGGCGATCAACTGGGTGGTGCGTCGTAT
GTCGCTCCCCGCAGGGGAGCGTGGATTGAAAC	ACGGACACACCCAGCGCCTGCAGCACGTCCGCGAC
GTCGCTCCCCGCAGGGGAGCGTAGATTGAAAC	ACCCCTTGACTACCACTACCACGACGCAAAAAGC
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	GGAAGCTAACATATCACCGAACACCCGTTCGTGA
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	GACTGACGCACGGCCTGCGGACGTTCGCGGAAC
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	TCTCCACAAAAGCCTCTATCATAATAAACAAGG
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	GCCGCCTGGCGAGACGCGACGCCGATGCACAACGATC
GTCGCTTCCCGTGGGGGAGCGTGAATTGAAAC	GTCTGGTTCTTTATATGAGACAACGTCTCAAGAT
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	TGGCCGCCATGCTCGTCTTGTTCGGGCGGGGGTGACG
GTCGCTCCCCGTGGGGGAGCGTGGATTGAAAC	TCAGCAAAGAGTCGTGCATTTTGGAAATGAAGCAGAT
GTCGCTCCCCGCAGGGGAGCGTGGATTGAAAC	TCCACGGCCTCGAGATCCAACGGGATACCGGCC
GTCGTTCCCCGCCGGGGAGCATGATTTGAAAC

>NZ_CP045802|15|3|2512402-2514343|PILER-CR
GGGGAGCGTGGATTGAAAC	ACCCTTTCTCGCTGTTCGGCGGAAGGCCCGACGGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	GTTCGTGTTTAAGAGTCAAAATAGCTTCAGCTGCTGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	CCCAGGCGAGGCCCTATTCGGAAGTACGGTCGAGGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	TTTTCCCGCCTTGGCGAGGATCGCCATATAGTCGGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	GCCGGCGGGGTTGGAAAGGCGTGAACCATGCTGGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	ACCTTGTCCAACTGGCACCGGCGCGGGCGCGACGTCGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	CTCGAATCGAAGGGCTTCACGGTGGTTCGTCACTAGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	GCTCGTTCGGCACGGTCATTCGCGACGTGCTGGAGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	AATAAGACGCATGAGTTGCCGGTAGACCATCGACGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	CAATTCTTTAATAATGGCTTGAATTGCTTTTTCTGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	CCATATATCGGCATATCCACAATGCGCTACTTTAGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	CATTGCCGCTGGATCGACTCCCGCGCCTCCTGCGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	TCATATATGCAAATGATGGAAGCTGTGCATGCAGTCGCTCCCCGCA
GGGGAGCGTGGATTGAAAC	GCAAAAGCCGCAATCGTATGAAGCCTGCGAACGTCGTCGCTCCCCGCA
GGGGAGAGTGGATTGAAAC	CATTCGCAGATACCGATAATTCTCATTCTCGACTCGTCGCTCCCCGCA
GGGGAGCGTGGATTGAAAC	CGCAGCGGGAAATTGGCAAAGACCTGCGATCCGTGTCGCTCCCCGCA
GGGGAGCGTGGATTGAAAC	ACCGAGCCAGAGCCGCGAAAAGGAGAAGAGGGCGTCGCTCCCGCA
GGGGAGCGTGGATTGAAAC	TGCTACTTGCCGGCCATCGTCGACTGGCCGTTATGTCGCTCCCCGCA
GGGGAGCGTGGATTGAAAC	TGGAGGACGCCTGCGATTTTCCCGAGGTCTTGGAGTCGCTCCCCGCA
GGGGAGCGTGGATTGAAAC	CTGATCTGGGCGATCAACTGGGTGGTGCGTCGTATGTCGCTCCCCGCA
GGGGAGCGTGGATTGAAAC	ACGGACACACCCAGCGCCTGCAGCACGTCCGCGACGTCGCTCCCCGCA
GGGGAGCGTAGATTGAAAC	ACCCCTTGACTACCACTACCACGACGCAAAAAGCGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	GGAAGCTAACATATCACCGAACACCCGTTCGTGAGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	GACTGACGCACGGCCTGCGGACGTTCGCGGAACGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	TCTCCACAAAAGCCTCTATCATAATAAACAAGGGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	GCCGCCTGGCGAGACGCGACGCCGATGCACAACGATCGTCGCTTCCCGTG
GGGGAGCGTGAATTGAAAC	GTCTGGTTCTTTATATGAGACAACGTCTCAAGATGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	TGGCCGCCATGCTCGTCTTGTTCGGGCGGGGGTGACGGTCGCTCCCCGTG
GGGGAGCGTGGATTGAAAC	TCAGCAAAGAGTCGTGCATTTTGGAAATGAAGCAGATGTCGCTCCCCGCA
GGGGAGCGTGGATTGAAAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_028599869.1|2511535_2512093_+|elongation-factor-P	unknown	unknown	gnl|CDD|234788
NZ_CP045802.1|WP_028599864.1|2518720_2518924_+|stage-III-sporulation-protein-AC	unknown	unknown	gnl|CDD|131895
NZ_CP045802.1|WP_153783450.1|2507830_2508157_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_101809010.1|2522054_2522753_+|hypothetical-protein	unknown	unknown	gnl|CDD|378918
NZ_CP045802.1|WP_052333436.1|2519348_2520560_+|stage-III-sporulation-protein-AE	unknown	unknown	gnl|CDD|213743
NZ_CP045802.1|WP_153783454.1|2520597_2521326_+|stage-III-sporulation-protein-AF	unknown	unknown	gnl|CDD|378212
NZ_CP045802.1|WP_028599866.1|2516753_2517020_+|YqhV-family-protein	unknown	unknown	gnl|CDD|378514
NZ_CP045802.1|WP_028599868.1|2514483_2515737_+|aspartate-kinase	unknown	unknown	gnl|CDD|235843
NZ_CP045802.1|WP_028599871.1|2509955_2510402_+|type-II-3-dehydroquinate-dehydratase	unknown	unknown	gnl|CDD|235443
NZ_CP045802.1|WP_028599859.1|2522997_2523486_+|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein	unknown	unknown	gnl|CDD|235777
NZ_CP045802.1|WP_028599870.1|2510443_2511511_+|aminopeptidase-P-family-protein	unknown	unknown	gnl|CDD|223085
NZ_CP045802.1|WP_153783453.1|2518947_2519343_+|stage-III-sporulation-protein-AD	unknown	unknown	gnl|CDD|131896
NZ_CP045802.1|WP_101809008.1|2518188_2518707_+|stage-III-sporulation-protein-AB	unknown	unknown	gnl|CDD|181372
NZ_CP045802.1|WP_153783451.1|2508188_2509169_-|DUF1385-domain-containing-protein	unknown	unknown	gnl|CDD|226390
NZ_CP045802.1|WP_028599861.1|2521342_2521987_+|stage-III-sporulation-protein-AG	unknown	unknown	gnl|CDD|274319
NZ_CP045802.1|WP_043111623.1|2506014_2507058_-|spore-photoproduct-lyase	unknown	unknown	gnl|CDD|213890
NZ_CP045802.1|WP_153783452.1|2509348_2509876_+|hypothetical-protein	unknown	unknown	gnl|CDD|314111
NZ_CP045802.1|WP_028599874.1|2507259_2507685_+|transcriptional-regulator-MntR	unknown	unknown	gnl|CDD|179669
NZ_CP045802.1|WP_028599876.1|2505291_2506002_+|cytochrome-C-biogenesis-protein-CcdA	unknown	unknown	gnl|CDD|280792
NZ_CP045802.1|WP_028599877.1|2503242_2505246_+|methionine--tRNA-ligase	unknown	unknown	gnl|CDD|237028

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_028599869.1|2511535_2512093_+|elongation-factor-P	gnl|CDD|234788	PRK00529, PRK00529, elongation factor P; Validated.	1.13872e-109
NZ_CP045802.1|WP_028599864.1|2518720_2518924_+|stage-III-sporulation-protein-AC	gnl|CDD|131895	TIGR02848, Stage_III_sporulation_protein_AC, stage III sporulation protein AC. Members of this protein family are designated SpoIIIAC, part of the spoIIIA operon of sporulation genes whose mutant phenotype is linked to sporulation stage III. Members of this family are encoded by the genome of a species if and only if that species is capable of endospore formation, as in Bacillus subtilis. The molecular function of this small, probable integral membrane protein is unknown. [Cellular processes, Sporulation and germination].	3.87684e-19
NZ_CP045802.1|WP_101809010.1|2522054_2522753_+|hypothetical-protein	gnl|CDD|378918	pfam12685, SpoIIIAH, SpoIIIAH-like protein. Stage III sporulation protein AH (SpoIIIAH) is a protein that is involved in forespore engulfment. It forms a channel with SpoIIIAH that is open on the forespore end and closed (or gated) on the mother cell end. This allows sigma-E-directed gene expression in the mother-cell compartment of the sporangium to trigger the activation of sigma-G forespore-specific gene expression by a pathway of intercellular signaling. This family of proteins is found in bacteria, archaea and eukaryotes and so must have a wider function that in sporulation. Proteins in this family are typically between 174 and 223 amino acids in length.	2.12163e-15
NZ_CP045802.1|WP_052333436.1|2519348_2520560_+|stage-III-sporulation-protein-AE	gnl|CDD|213743	TIGR02829, Stage_III_sporulation_protein_AE, stage III sporulation protein AE. A comparative genome analysis of all sequenced genomes of shows a number of proteins conserved strictly among the endospore-forming subset of the Firmicutes. This protein, a member of this panel, is found in a spore formation operon and is designated stage III sporulation protein AE. [Cellular processes, Sporulation and germination].	1.03306e-119
NZ_CP045802.1|WP_153783454.1|2520597_2521326_+|stage-III-sporulation-protein-AF	gnl|CDD|378212	pfam09581, Spore_III_AF, Stage III sporulation protein AF (Spore_III_AF). This family represents the stage III sporulation protein AF (Spore_III_AF) of the bacterial endospore formation program, which exists in some but not all members of the Firmicutes (formerly called low-GC Gram-positives). The C-terminal region of these proteins is poorly conserved.	1.40599e-27
NZ_CP045802.1|WP_028599866.1|2516753_2517020_+|YqhV-family-protein	gnl|CDD|378514	pfam10942, DUF2619, Protein of unknown function (DUF2619). This bacterial family of proteins has no known function.	1.21967e-23
NZ_CP045802.1|WP_028599868.1|2514483_2515737_+|aspartate-kinase	gnl|CDD|235843	PRK06635, PRK06635, aspartate kinase; Reviewed.	0
NZ_CP045802.1|WP_028599871.1|2509955_2510402_+|type-II-3-dehydroquinate-dehydratase	gnl|CDD|235443	PRK05395, PRK05395, type II 3-dehydroquinate dehydratase.	1.04992e-89
NZ_CP045802.1|WP_028599859.1|2522997_2523486_+|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein	gnl|CDD|235777	PRK06302, PRK06302, acetyl-CoA carboxylase biotin carboxyl carrier protein.	8.01354e-59
NZ_CP045802.1|WP_028599870.1|2510443_2511511_+|aminopeptidase-P-family-protein	gnl|CDD|223085	COG0006, PepP, Xaa-Pro aminopeptidase [Amino acid transport and metabolism].	1.01272e-122
NZ_CP045802.1|WP_153783453.1|2518947_2519343_+|stage-III-sporulation-protein-AD	gnl|CDD|131896	TIGR02849, Stage_III_sporulation_protein_AD, stage III sporulation protein AD. Members of this family are the uncharacterized protein SpoIIIAD, part of the spoIIIA operon that acts at sporulation stage III as part of a cascade of events leading to endospore formation. Note that the start sites of members of this family as annotated tend to be variable; quite a few members have apparent homologous protein-coding regions continuing upstream of the first available start codon. The length of the alignment and the scoring cutoff thresholds for the model have been set to try to detect all valid members of the family, even if annotation of the start site begins too far downstream. [Cellular processes, Sporulation and germination].	1.45054e-27
NZ_CP045802.1|WP_101809008.1|2518188_2518707_+|stage-III-sporulation-protein-AB	gnl|CDD|181372	PRK08307, PRK08307, stage III sporulation protein SpoAB; Provisional.	7.9027e-55
NZ_CP045802.1|WP_153783451.1|2508188_2509169_-|DUF1385-domain-containing-protein	gnl|CDD|226390	COG3872, COG3872, Predicted metal-dependent enzyme [General function prediction only].	1.23455e-124
NZ_CP045802.1|WP_028599861.1|2521342_2521987_+|stage-III-sporulation-protein-AG	gnl|CDD|274319	TIGR02830, Stage_III_sporulation_protein_AG, stage III sporulation protein AG. CC A comparative genome analysis of all sequenced genomes of shows a number of proteins conserved strictly among the endospore-forming subset of the Firmicutes. This protein, a member of this panel, is found in a spore formation operon and is designated stage III sporulation protein AG. [Cellular processes, Sporulation and germination].	1.38738e-43
NZ_CP045802.1|WP_043111623.1|2506014_2507058_-|spore-photoproduct-lyase	gnl|CDD|213890	TIGR04070, photo_TT_lyase, spore photoproduct lyase. DNA damage to bacterial spores from ultraviolet light accumulates in the form of 5-thyminyl-5,6-dihydrothymine, spore photoproduct. The damage is repaired by spore photoproduct lyase, a member of the radical SAM family of enzymes. The score of this model is set to restrict itself to spore-forming members of the Firmicutes, but additional homologs scoring below the trusted cutoff tend to occur in radioresistant organisms (e.g. Kineococcus radiotolerans) and may be functionally equivalent. A related family in the Mycobacterium lineage is described by family TIGR03886, and may or may not be equivalent in function. [DNA metabolism, DNA replication, recombination, and repair, Cellular processes, Sporulation and germination].	0
NZ_CP045802.1|WP_153783452.1|2509348_2509876_+|hypothetical-protein	gnl|CDD|314111	pfam11085, YqhR, Conserved membrane protein YqhR. This family is conserved in the Bacillaceae family of the Firmicutes. The function is not known.	2.45075e-30
NZ_CP045802.1|WP_028599874.1|2507259_2507685_+|transcriptional-regulator-MntR	gnl|CDD|179669	PRK03902, PRK03902, transcriptional regulator MntR.	2.91354e-83
NZ_CP045802.1|WP_028599876.1|2505291_2506002_+|cytochrome-C-biogenesis-protein-CcdA	gnl|CDD|280792	pfam02683, DsbD, Cytochrome C biogenesis protein transmembrane region. This family consists of the transmembrane (i.e. non-catalytic) region of Cytochrome C biogenesis proteins also known as disulphide interchange proteins. These proteins posses a protein disulphide isomerase like domain that is not found within the aligned region of this family.	1.67174e-47
NZ_CP045802.1|WP_028599877.1|2503242_2505246_+|methionine--tRNA-ligase	gnl|CDD|237028	PRK12267, PRK12267, methionyl-tRNA synthetase; Reviewed.	0

Protein sequences

>NZ_CP045802.1|WP_028599869.1|2511535_2512093_+|elongation-factor-P
MISVNDFKTGLTIEVDTDIFTVIEFQHVKPGKGAAFVRSKLKNLRNGNIVEKTFRAGETLGRAHVENREVQYLYNSGSEYTFMDNESFDQFNLDKKQLEWEINFLKENMNVNIASYKGEIIGITMPNSVELKVAETEPGVKGNTAQGATKNATLETGYTVQVPLFINEGDLLLIDTREGRYISRA
>NZ_CP045802.1|WP_028599870.1|2510443_2511511_+|aminopeptidase-P-family-protein
MAQRLDKLREKLASQGLEALLIGSAYNRQYISGFTGSAGWVLVAADRAWFLTDFRYTEQAAEQVHGFDIVEHGPDPIASIGDLLRGAGLSKLGFEENHTTYAQFAKWSKTLQGVELVPVPGLVEELRMIKDEAELAVMQEAADLADRAFSYIQGLIKPGMKESDIALELEVFLRSGGAASSCFDTIVASGERSALPHGVASDRVIGSNEFVKLDFGALYRGYCSDITRTVAVGQVSDKHREIYDIVLEAQLHALEHIRPGMTGKQADALARDVIAKHGYGDRFGHSLGHGLGMEVHEQPSLSVRSDIVLVPGMVVTVEPGIYIPGFGGVRIEDDIVLTDDGIRILTSSTKQLITL
>NZ_CP045802.1|WP_028599871.1|2509955_2510402_+|type-II-3-dehydroquinate-dehydratase
MIRILVLNGPNLNMLGVREPGIYGSATLQDIEAMLRGIAETAGAELEFRQSNHEGELIDLIHAAHGSADGILLNPGALTHYSYALRDALGSVSVPAVEVHLSNIHKREAFRHVSVTAAAAIGQIAGFGPASYSLGLTALLDHLKAGGQ
>NZ_CP045802.1|WP_153783452.1|2509348_2509876_+|hypothetical-protein
MSASAASREASSASRRSRRSRRVTNPWSYCASLGFWAGLFWGTIRWLLYTFKFTSVLPAFLADPFFRRSFLVTGWGHGTGIAAFIVFSIVAAYLYKLLLGRFRGPWAGFFYGLLWWTLLFLAFGPLLGMMEPVTRIGWNSIFTEISLFIVWGMFIGYSIAFEFNDEASREPRKEP
>NZ_CP045802.1|WP_153783451.1|2508188_2509169_-|DUF1385-domain-containing-protein
MPEPTTSIYGGQAVIEGVMFGGRNVNVTAVRRKNDEIAYYEVPASRKKPWYQPLKKVPFVRGVIGILESSARGSQHLNFSMEAYAEDNEEKDEASAADSSKPKPEKKEGWSLAMVFGVAVAGVISFILGKVVFTAVPAIVEDLLFQGRFGNIVIHNLLEGAIKILFLLAYLYLLSLTPMIKRLFQYHGAEHKVITAYEHGDELTVENVQRRTRLHYRCGSSFIIFSVLVGVIVYSFFTWDTLWERVYIRLLLLPVVLGVSYEVLRFTNSLREVPVLRFLGYPGLWLQLLTTKEPTDDQVAVSIASFKRMRELEQQVNEPQPAGAAV
>NZ_CP045802.1|WP_153783450.1|2507830_2508157_-|hypothetical-protein
MKRRTATIWMAVLAFLALIGLVQMVLSRNFTALLPLVVLALIFGLYRLSPAGRASRAARPRVKPGRAAAASSAGKPRQAAAAKPRSRKASPFRVIEGGKDEDGMPKYH
>NZ_CP045802.1|WP_028599874.1|2507259_2507685_+|transcriptional-regulator-MntR
MPTPSMEDYLERIYKLIEEKGYARVSDIAEGLEVHPSSVTKMIQKLDKDQYLIYEKYRGLVLTSKGKKMGKRLVERHHLLEEFLELIGVQEENIYRDVEGIEHHLSWDSITCIETLVEYFRRDSERLESLRGLRGELEADS
>NZ_CP045802.1|WP_043111623.1|2506014_2507058_-|spore-photoproduct-lyase
MERPPARLESFVPELVYFEPDALSYPKGKRIYEWAVQQGLPVRMTTSHNRITDLPGESELEKYRIAKRTLVVGLRKTLKFDTSKPSAEYAIPIATGCMAHCHYCYLQTTLGAKPYVRVYVNTEEIMDAARGYIAERAPQITRFEAACTSDPVGLEPISGSLAELIEFMADQELGRLRFVTKFHHVDSLLGLRHNGHTRIRFSVNARYVIKNFEPATSSFEQRIEAAGKVARAGYPIGFLIAPIIWHDGWEEGYAELLDRLAKALPSGVPDLTFELIQHRFTKTAKNTIEKRYPKTKLEMDIEKRKYKWGRWGQGKYVYPDEQADALRMFISERIFDRFPQATIDYFT
>NZ_CP045802.1|WP_028599876.1|2505291_2506002_+|cytochrome-C-biogenesis-protein-CcdA
MSSINIGLAFIGGIASFISPCCLPLYPSYLSYITGISVADLKSEKPGAEVRRRTMTHTLFFILGFSVVYYTLGYSTNKFAELFSDYQDLIRMLSAILIMLMGLFLLGLFQPRALMRDFKLPVKRGSGYLGSFIFGIGFSAGWSPCIGPILAGILALAASDPGTWFSLTTAYALGFAIPFFLLAFFIGSARWILKYSSLLMKLGGGLMLVMGVLLFTDRMYIITVYLNSITPDWLKF
>NZ_CP045802.1|WP_028599877.1|2503242_2505246_+|methionine--tRNA-ligase
MSSETKSFYITTPIYYPSGKLHIGHAYCTLAGDAMARYKRARGYDVWYLTGTDEHGQKIERSAKEEGLTPIQFLDRNVSEIQKLWAKLEISHDDFIRTTEERHKLSAQKIFKQLLDQGDIYKGTYEGWYCTPCESFFTERQLENGNCPDCGRPVELVKEESYFFRMSKYADRLLSYYEEHPEFIQPESRKNEMINNFIKPGLEDLAVSRATFDWGIQVPNDPEHVIYVWIDALSNYITALGYGSDDESAYRKFWPADVHLVGKEIVRFHTIYWPIMLMALDLPLPKKVFGHGWWLVKEGKMSKSKGNVIDPVVLLDRYGLDALRYFLLREVPFGSDGTFTPEGFVERLNFDLANDLGNLLNRTVAMIDKYFGGEIPAYAGKVTPFDEALEKQAADSIAAVEEAMESMQFSVALSAIWQLVSRTNKYIDETQPWVLAKDEARRAELASAMHHLAESLRIVSVLLTPFMSRAPREIRVQLGVEEGPLASWDSAREFGSLPGGTRVAKGSPLFPRLDAEEEIAYIVSAISGGSKPAEAPAAEAAASAAALPAAAEPVEAPELKEEIGIDDFAKVELRVAQVIAAEPVPKADKLLKLQLDLGFEQRQVVSGIAKFYKPEELVGRKVICVTNLKPVKLRGELSRGMILAASQGDQLTLATVPDSMPNGAVVK
>NZ_CP045802.1|WP_028599868.1|2514483_2515737_+|aspartate-kinase
MSLIVMKFGGSSVGTTERMQRVAQRIVENRDAGHKVVVVVSAMGDTTDDLIDQSKRLNPNPPAREMDMLLTTGEQISVALLSMTIHAMGRKAVSMTGWQAGIRTEPLHGKARITDIQPDRIHAALEEGGIVIVAGFQGMTEQGEITTLGRGGSDTTAVALAAAIEADVCEIFTDVDGIYSTDPRVVKNARKLPEISYDEMLELAHLGAAVLHPRAVEYAKHNNVKLVVRSSFTHNEGTTVKEEAVMEQGIVVRGIAFDKDVARISILGVEDVPGVLAGVFGALADGGIDVDMIVQSGVQDGKADFSFTVAGGDAEQAVSIIAGIRSEVPYRETTSETGLVKVSIVGAGMVSNPGVAARMFRAISDLGVSIKMVSTSEIKTSCVIAAEPLQDVVRALHTTYGLDTAEQVFVGGPSERR
>NZ_CP045802.1|WP_028599866.1|2516753_2517020_+|YqhV-family-protein
MLNKAVAAMASLRLVSGSIEIMAALLMLRLNQVDKALAVNSALALVGPIVLLTTTAIGLIGLSDKLSPSRMLWIGTGVACLLIGVLKK
>NZ_CP045802.1|WP_101809008.1|2518188_2518707_+|stage-III-sporulation-protein-AB
MIKAAGAVLVLIAGTLIGFLQAARFARRPKQLRELAHGLQRLETEIGYGYTPLPEALRRVAAQTSEPLASMLLSPADDIESGRSADFQAGWEASIQAYGPRTALKAPELASLRRLGSILGMSDREDQLKHLKLAQQQLLAEESGARDDQARYEKLSRALGILLAALVVILIV
>NZ_CP045802.1|WP_028599864.1|2518720_2518924_+|stage-III-sporulation-protein-AC
MTMDISAIFQIAGIGIIVAMIHTVLKQMGKEDMAHWVTLIGFVVVLFMVVRMLNDLFQEIKTIFLFQ
>NZ_CP045802.1|WP_153783453.1|2518947_2519343_+|stage-III-sporulation-protein-AD
MEMVHIAGIGLLAAILVLVLKEQKPLFAFLLAMFAGIFIFLLMIGRIEAVIGTMQQLAERSGIPSVYLKTILKMIGIAYIAEFAAQIIRDAGAEGVASKVEFAGKVLILVLAVPIINVIVETVVGLLPAGG
>NZ_CP045802.1|WP_052333436.1|2519348_2520560_+|stage-III-sporulation-protein-AE
MRFKLALLWLLLAAWGLGLAPAASAQPPDGGDGSRTAAGITEELAREQAQSYGTDAVESYWDDLVRQYGGYFPEGTMPSFLEMVAPGGQGLKASDVLKGLLAMLTHEVLYNGKLLVSIVLLAVFSSILQTLQSAFERQTVSQVAYAVAYMVLIVLAVNSFHVAIGYAKDAIETMIQFMMAMVPLLMTLIASSGGIATVTLLHPVIIFMVHLVGTLIYTVVFPLLFFSAVLHIASAMSDRFKVTQLANMLRTIGAGLLGVMLTVFLGVVSIQGATGSMTDGVTLRTAKFISGSFVPVVGKTFSDAADTVISASMLAKNAVGLAGVIILLFISAFPAIKILVLAVIYNACGAVLQPLGASPITTCLSTIGKTMLYVFGALAAVSLMFFLAVTILLTAGNAAIMMR
>NZ_CP045802.1|WP_153783454.1|2520597_2521326_+|stage-III-sporulation-protein-AF
MLDWLSSWLKDVVAVVLLAALVDLLLPNQRMQRYARLVTGLIVLLVILTPLLRLVQGDFQTRLETGYREWNRELERSQVKMPSLDEILRQAEIAAGRSGEQAVALARTQLEMGIREAVERETGAAVKEVAAAVAWDGQGGGEIRSVNVRLAAAPSGEVLPAEAAAADDASAGEASIEPVKPVEPVEVRLSEPEAQEAMAGMGEASPRKADARLESRIRQIVSGSWPIGAAQVSVELEPADGS
>NZ_CP045802.1|WP_028599861.1|2521342_2521987_+|stage-III-sporulation-protein-AG
MANWWEKLRQAAAGGAEGPSRIKSLRWLLVLGGIGVLLILAGNVLNFRDVGTLPSGDAAPPPAAEDQAALGGRVQSPGTDFGGIEAPLEARLKDILEKIVGVGEVDVLVTVDSTEENVWGKDDNTSQQVTDETDKSGGKRHVTQMTSSGKIVMYEVSGEQKPVVTKIVKPKVRGVLVVANGAENATVRRIIAEAVERGMDVPLSAISIVPRKTG
>NZ_CP045802.1|WP_101809010.1|2522054_2522753_+|hypothetical-protein
MNSKRQTIWLVSMLSLMVVLSAYYLFTEDAGTKGLADTAQTQAGAAEVSQTDGIEVQQVTGDGALDAEAAAEAAETAESAESAEPGKDAAGADKETAADGGLSPEDQAVLQQYESSGSSSQFTELGLRSQERVNAEYDKIMQKISDVKSDSETSAKAVTELEGFEERQSKLTELRGQLEKEFKNVVIDENGDAVKVVVQSQKLERSQAAAIISTVSAALDVNAGDVLVQYLP
>NZ_CP045802.1|WP_028599859.1|2522997_2523486_+|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein
MFKLNEIKELIKLIDQTSVHEFEIENEGTKLAIRKPGKAETVFVQGAPAISTYTAPAAEPAASVAAAAPASAAPAASAAPKENLHQIVSPMVGTFYAASTPDSPPYVSPGSKVTEKSVVCILEAMKLMNELEAEVRGEIVEVLVQNGQLVEYGQPLFTVRPE

Crispr_ID: NZ_CP045802_16

• CRISPR_ID: NZ_CP045802_16
• CRISPR_location: 3388269-3389068
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 15 spacers

Consensus repeat of NZ_CP045802_16

Consensus_repeat	Method
CAAGGCACTTTGNGTGCCCTGGATTCGAGATTG	CRT

spacers of NZ_CP045802_16

>16.1|3388302|18|NZ_CP045802|CRT
GATTGGTTCTCGCTGATT
>16.2|3388353|19|NZ_CP045802|CRT
GATTGGGTTTCGCCTGATT
>16.3|3388405|18|NZ_CP045802|CRT
GTTTGGGTTTCGCTGGTT
>16.4|3388456|18|NZ_CP045802|CRT
GTCTAGGTTTCGCTGGTT
>16.5|3388507|18|NZ_CP045802|CRT
GTCTGGGTTTCGCTGATT
>16.6|3388558|18|NZ_CP045802|CRT
GGCACGTTCCCACTGATC
>16.7|3388609|18|NZ_CP045802|CRT
GTCTGGGTTTCGCTGATT
>16.8|3388660|18|NZ_CP045802|CRT
GTTTGGGTTTCGCTGTTT
>16.9|3388711|18|NZ_CP045802|CRT
GTTTGGGTTTCGCTGTTT
>16.10|3388762|18|NZ_CP045802|CRT
GGCTCGTCTTCGATGATT
>16.11|3388813|18|NZ_CP045802|CRT
GGCTCGTCTTTGATGGTT
>16.12|3388864|18|NZ_CP045802|CRT
GGCTCGTCTTCGATGATT
>16.13|3388915|19|NZ_CP045802|CRT
GTTTGGGTTTCGCCTGATT
>16.14|3388967|18|NZ_CP045802|CRT
AGCACGTCTTCGCAGATC
>16.15|3389018|18|NZ_CP045802|CRT
GGCTCGTTCCCGCTGATT

CRISPR arrays and Neighbor proteins around NZ_CP045802_16

CRISPR arrays

The CRISPR arrays of NZ_CP045802_16

>merge|NZ_CP045802|16|3388269-3389068|CRT
CAAGGCACTCTGGGTGCCTTGGATTCGAGATTGGATTGGTTCTCGCTGATTCAAGGCACTTTGAGTGCCCTGGATTCGAGATTTGATTGGGTTTCGCCTGATTCAAGGCACTCTGAGTGCCTTGGATTCGAGATTGGTTTGGGTTTCGCTGGTTCAAGGCACTTTGAGTGCCTTGGATTCGAGATTGGTCTAGGTTTCGCTGGTTCAAGGCACTTTGGGTGCCCTGAATTCGAGATTCGTCTGGGTTTCGCTGATTCAAGGCACTTTGGGTGCCCTGGAATCGAGATTGGGCACGTTCCCACTGATCCAAGGCACTTTGAGTGCCTTGGATTCGAGATTCGTCTGGGTTTCGCTGATTCAAGGCACTTTGAGTGCCCTGGATTCGAGATTGGTTTGGGTTTCGCTGTTTCAAGGCACTTTGAGTGCCCTGGATTCGAGATTGGTTTGGGTTTCGCTGTTTCAAGGCACTTTGAGTGCCCTGGATTCGAGATCGGGCTCGTCTTCGATGATTCAAGGCACTTTGAGTGCCCTAGATTCGAGATTGGGCTCGTCTTTGATGGTTCAAGGCACTTTGGGTGCCCTGAATTCGAGATCGGGCTCGTCTTCGATGATTCAAGGCACTTTGAGTGCCCTGGATTCGAGATTGGTTTGGGTTTCGCCTGATTCAAGGCACTTTGGGTGCCCTGGATTCGAGATTGAGCACGTCTTCGCAGATCCAAGGCACTTTCGGTGCCCTGGATTCGAGATTGGGCTCGTTCCCGCTGATTCAAGGCACTTTGGGTGCCCTGGATTCGAGATTG

>NZ_CP045802|16|4|3388269-3389068|CRT
CAAGGCACTCTGGGTGCCTTGGATTCGAGATTG	GATTGGTTCTCGCTGATT
CAAGGCACTTTGAGTGCCCTGGATTCGAGATTT	GATTGGGTTTCGCCTGATT
CAAGGCACTCTGAGTGCCTTGGATTCGAGATTG	GTTTGGGTTTCGCTGGTT
CAAGGCACTTTGAGTGCCTTGGATTCGAGATTG	GTCTAGGTTTCGCTGGTT
CAAGGCACTTTGGGTGCCCTGAATTCGAGATTC	GTCTGGGTTTCGCTGATT
CAAGGCACTTTGGGTGCCCTGGAATCGAGATTG	GGCACGTTCCCACTGATC
CAAGGCACTTTGAGTGCCTTGGATTCGAGATTC	GTCTGGGTTTCGCTGATT
CAAGGCACTTTGAGTGCCCTGGATTCGAGATTG	GTTTGGGTTTCGCTGTTT
CAAGGCACTTTGAGTGCCCTGGATTCGAGATTG	GTTTGGGTTTCGCTGTTT
CAAGGCACTTTGAGTGCCCTGGATTCGAGATCG	GGCTCGTCTTCGATGATT
CAAGGCACTTTGAGTGCCCTAGATTCGAGATTG	GGCTCGTCTTTGATGGTT
CAAGGCACTTTGGGTGCCCTGAATTCGAGATCG	GGCTCGTCTTCGATGATT
CAAGGCACTTTGAGTGCCCTGGATTCGAGATTG	GTTTGGGTTTCGCCTGATT
CAAGGCACTTTGGGTGCCCTGGATTCGAGATTG	AGCACGTCTTCGCAGATC
CAAGGCACTTTCGGTGCCCTGGATTCGAGATTG	GGCTCGTTCCCGCTGATT
CAAGGCACTTTGGGTGCCCTGGATTCGAGATTG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_153783747.1|3391918_3392998_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223674
NZ_CP045802.1|WP_153783750.1|3398647_3400432_-|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|225519
NZ_CP045802.1|WP_101809250.1|3385396_3385987_-|16S-rRNA-(guanine(966)-N(2))-methyltransferase-RsmD	unknown	unknown	gnl|CDD|223813
NZ_CP045802.1|WP_153783743.1|3384849_3385413_-|pantetheine-phosphate-adenylyltransferase	unknown	unknown	gnl|CDD|234674
NZ_CP045802.1|WP_028597466.1|3378300_3379302_-|phosphate-acyltransferase-PlsX	unknown	unknown	gnl|CDD|235414
NZ_CP045802.1|WP_153783748.1|3392985_3394701_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|173883
NZ_CP045802.1|WP_153783751.1|3400541_3401378_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223472
NZ_CP045802.1|WP_028596831.1|3394975_3395392_-|nickel-responsive-transcriptional-regulator-NikR	unknown	unknown	gnl|CDD|179855
NZ_CP045802.1|WP_153784744.1|3395653_3396919_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_CP045802.1|WP_028597467.1|3379298_3379904_-|transcription-factor-FapR	unknown	unknown	gnl|CDD|179847
NZ_CP045802.1|WP_153783740.1|3380913_3382158_+|nucleotidyltransferase	unknown	unknown	gnl|CDD|377535
NZ_CP045802.1|WP_153783742.1|3383378_3384740_+|hypothetical-protein	unknown	unknown	gnl|CDD|274333
NZ_CP045802.1|WP_153783746.1|3389979_3390987_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|223521
NZ_CP045802.1|WP_153783741.1|3382425_3383280_-|hypothetical-protein	unknown	unknown	gnl|CDD|226011
NZ_CP045802.1|WP_153784743.1|3391040_3391904_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|224094
NZ_CP045802.1|WP_153783739.1|3380272_3380776_-|DUF177-domain-containing-protein	unknown	unknown	gnl|CDD|376863
NZ_CP045802.1|WP_153783749.1|3397050_3398673_-|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_CP045802.1|WP_153783745.1|3389129_3389756_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|224049
NZ_CP045802.1|WP_028597468.1|3380048_3380222_-|50S-ribosomal-protein-L32	unknown	unknown	gnl|CDD|237038
NZ_CP045802.1|WP_153783744.1|3386225_3388106_+|chitinase	unknown	unknown	gnl|CDD|119350

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_153783747.1|3391918_3392998_-|ABC-transporter-permease-subunit	gnl|CDD|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	4.03313e-103
NZ_CP045802.1|WP_153783750.1|3398647_3400432_-|HAMP-domain-containing-protein	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	2.42148e-63
NZ_CP045802.1|WP_101809250.1|3385396_3385987_-|16S-rRNA-(guanine(966)-N(2))-methyltransferase-RsmD	gnl|CDD|223813	COG0742, COG0742, N6-adenine-specific methylase [DNA replication, recombination, and repair].	3.38723e-66
NZ_CP045802.1|WP_153783743.1|3384849_3385413_-|pantetheine-phosphate-adenylyltransferase	gnl|CDD|234674	PRK00168, coaD, phosphopantetheine adenylyltransferase; Provisional.	8.35287e-98
NZ_CP045802.1|WP_028597466.1|3378300_3379302_-|phosphate-acyltransferase-PlsX	gnl|CDD|235414	PRK05331, PRK05331, phosphate acyltransferase PlsX.	1.17179e-177
NZ_CP045802.1|WP_153783748.1|3392985_3394701_-|ABC-transporter-substrate-binding-protein	gnl|CDD|173883	cd08518, PBP2_NikA_DppA_OppA_like_19, The substrate-binding component of an uncharacterized ABC-type nickel/dipeptide/oligopeptide-like import system contains the type 2 periplasmic binding fold. This CD represents the substrate-binding domain of an uncharacterized ATP-binding cassette (ABC) type nickel/dipeptide/oligopeptide-like transporter. The oligopeptide-binding protein OppA and the dipeptide-binding protein DppA show significant sequence similarity to NikA, the initial nickel receptor. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	0
NZ_CP045802.1|WP_153783751.1|3400541_3401378_-|ABC-transporter-permease-subunit	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	4.57249e-83
NZ_CP045802.1|WP_028596831.1|3394975_3395392_-|nickel-responsive-transcriptional-regulator-NikR	gnl|CDD|179855	PRK04460, PRK04460, nickel-responsive transcriptional regulator NikR.	1.13224e-45
NZ_CP045802.1|WP_153784744.1|3395653_3396919_-|extracellular-solute-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.69393e-49
NZ_CP045802.1|WP_028597467.1|3379298_3379904_-|transcription-factor-FapR	gnl|CDD|179847	PRK04424, PRK04424, transcription factor FapR.	1.60304e-101
NZ_CP045802.1|WP_153783740.1|3380913_3382158_+|nucleotidyltransferase	gnl|CDD|377535	pfam05636, HIGH_NTase1, HIGH Nucleotidyl Transferase. This family consists of HIGH Nucleotidyl Transferases.	8.25866e-169
NZ_CP045802.1|WP_153783742.1|3383378_3384740_+|hypothetical-protein	gnl|CDD|274333	TIGR02871, conserved_hypothetical_protein, sporulation integral membrane protein YlbJ. Members of this protein family are found exclusively in Firmicutes (low-GC Gram-positive bacterial) and are known from studies in Bacillus subtilis to be part of the sigma-E regulon. Mutation leads to a sporulation defect, confirming that members of this protein family, YlbJ, are sporulation proteins. This protein appears to be universal among endospore-forming bacteria, but is encoded by a pair ORFs distant from eash other in Symbiobacterium thermophilum IAM14863. [Cellular processes, Sporulation and germination].	1.98452e-34
NZ_CP045802.1|WP_153783746.1|3389979_3390987_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	4.35864e-91
NZ_CP045802.1|WP_153783741.1|3382425_3383280_-|hypothetical-protein	gnl|CDD|226011	COG3480, SdrC, Predicted secreted protein containing a PDZ domain [Signal transduction mechanisms].	1.36307e-23
NZ_CP045802.1|WP_153784743.1|3391040_3391904_-|ABC-transporter-permease-subunit	gnl|CDD|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	6.22945e-68
NZ_CP045802.1|WP_153783739.1|3380272_3380776_-|DUF177-domain-containing-protein	gnl|CDD|376863	pfam02620, DUF177, Uncharacterized ACR, COG1399. This family is nearly universally conserved in bacteria and plants except the Chlorophyceae algae. Thus far, mutantional analysis in bacteria have not established a function. In contrast, mutants have embryo lethal phenotypes in maize and Arabidopsis. In maize, the mutant embryos arrest at an early transition stage.It has been suggested that family members specifically affect 23S rRNA accumulation in plastids as well as bacteria.	1.49467e-29
NZ_CP045802.1|WP_153783749.1|3397050_3398673_-|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	3.28535e-53
NZ_CP045802.1|WP_153783745.1|3389129_3389756_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|224049	COG1124, DppF, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	4.13948e-72
NZ_CP045802.1|WP_028597468.1|3380048_3380222_-|50S-ribosomal-protein-L32	gnl|CDD|237038	PRK12286, rpmF, 50S ribosomal protein L32; Reviewed.	1.40627e-27
NZ_CP045802.1|WP_153783744.1|3386225_3388106_+|chitinase	gnl|CDD|119350	cd02871, GH18_chitinase_D-like, GH18 domain of Chitinase D (ChiD). ChiD, a chitinase found in Bacillus circulans, hydrolyzes the 1,4-beta-linkages of N-acetylglucosamine in chitin and chitodextrins. The domain architecture of ChiD includes a catalytic glycosyl hydrolase family 18 (GH18) domain, a chitin-binding domain, and a fibronectin type III domain. The chitin-binding and fibronectin type III domains are located either N-terminal or C-terminal to the catalytic domain. This family includes exochitinase Chi36 from Bacillus cereus.	7.76721e-133

Protein sequences

>NZ_CP045802.1|WP_153783744.1|3386225_3388106_+|chitinase
MEGNSFPYPKEENHLTPTRFKLPRRLAAACLSLALAAGLSAAALSAPKAAEAAPAGGYKIVGYWHNFDNGSGFIRLRDVSPDFDVVNVSFAEPVGGSSTGNIGFAPYNYTEADFKADVAYLKSQGKKVLISIGGANGQVQLASTAARDAFVSSVSGIIDKYGFDGLDVDFEGHSLYLNAGDSDFKNPTTPVIVNLISALKTIDARYGSDKFVLTMAPETFFVQLGYSFYGGSCISCDSRAGAYLPVIHATRDILDWLQVQNYNSGPITGLDDQYHTMGNADFHVAMADMLLTGFPVAKNAASFFPPLRQEQVLLGLPANGNAGGGFTSVAEVQKALDALIKGQQLSTYKTRGSSTGYPNFGGLMTWSVNWDKFNGFEFSRQHRAYLNAIAPSAPDTQPPTAPANVVSTAKTASSVSLSWGASTDNRGVTGYVVYYGGSSLQTSGTSATVAGLTANTAYTFTVKAKDAAGNLSAASAPLSVTTSAPSADTTPPTAPGSLAATAKTASSVTLGWSASTDNVGVTGYVVTYGTTSVETAVTSLAVTGLSPSTAYTFAVKAKDAAGNLSAAASLTVTTDAASGAQAWAAGVSYKTGDLVTYGGKTYSCRQPHTSLQGWEPPNVPALWLLK
>NZ_CP045802.1|WP_101809250.1|3385396_3385987_-|16S-rRNA-(guanine(966)-N(2))-methyltransferase-RsmD
MRVIAGEAKGRALKAVPGMNTRPTTDKVKEAIFSMIGPYFDGGWALDLFAGTGGLGIEALSRGMDKAVFVDMDRASVAVVRANVAAAGMAARAEIYTNEAGRAVKALQKRGQRFSAVFLDPPYRLTHMDELIAELQERELLADDAVIVVEHDASRAYPERIGAWERSKRAEYGETAVTVYRRREDGNTEAADGQEG
>NZ_CP045802.1|WP_153783743.1|3384849_3385413_-|pantetheine-phosphate-adenylyltransferase
MDKKDRHLEGTTGAEAEPAAGTAGKGRIAVYPGSFDPVTCGHLDIIQRAARQFDTVIVAVLNNTSKNPLFSVEERKRLLVEITKDIPNVEVDSFRDLTVRFMRSRGASTIVRGIRTVTDFEYELQLASMNHRLDEEIETIFMMTNPKYSYLSSSMVKEIARFQGSVKDLVPPAVERELLLKYPDRPE
>NZ_CP045802.1|WP_153783742.1|3383378_3384740_+|hypothetical-protein
MLRTLLTACAAILVVAAIVGGTSEAFQASLSGLSLWWNFVFPAVLPFLVLAELMLAFGLVDGLGVLLAPLMRQLRLPGSAGWALVQGWTSGYPAGSSAAARLVRSQRLTPAQGQRLLALVHSPNPLFVIVVLGAGFLHQPLFGLLLLPLLWAGSLLAAWTMSRLAPLSAAETKTTSADGASASAAAAEPSGLTGAGSRDASGSDREGAPAAEGPPAPVAMRPAATRASLAARALQAVEEGRARDGRSFGKALGDGVNGAVQQLMAAGGLIILASVLLRLLQPLLPAAIAGPGLTAAAEAHLGAAALASWHAPEPASLLQAAALAAALGWGGLCALLQAGGAASGSGLRLLPLAGSRLLAAAYSGGLALLLWRPLSSLAGSAAPAFADAGWAPPTGWAAGAQRLLQEPGAWSGVLRGALLLQLPLAAALVSALLLLSAAAALALRLRRSARTEA
>NZ_CP045802.1|WP_153783741.1|3382425_3383280_-|hypothetical-protein
MREKRTGLAPRASIRRWLPALALAGFVAAAALPRPYYVQTAGFARNAAPLIQFGAAMEGREAEAAAAATGPAWLYTAVKLERASLLEAAYAELTGRGDALSVRSVLGGASEEAYRIRMEEAMRQALLLAARAAADEAKREVVEAEGEAGTSEREAEKAGSQPSGLRLADGGREPLWLGAAAAGGPSAGLMAALSLYDRLTPDAELLGGRRIAGTGTIDAAGRIGAVGGVARKAQAAAEAGAGLFVAPKSEAGEAEKAARRAGGRMRVVGADTLAEAVALLQPRP
>NZ_CP045802.1|WP_153783740.1|3380913_3382158_+|nucleotidyltransferase
MRTVGLIVEYNPFHHGHAYHLQKSKEAAVAEASVAVMSGSFLQRGEPALMDKWARTRTALEGGIDLVLELPLAYAVQPAEWFAYGAVWTLEATGVVDAFCFGSETGELAPLRAAARLLAEEPESFRAALASGLERGLPYPSAYSAAAAELLRRDGGAEFPPLAAEQLAQPNMTLGLHYLLALERLGGRMEPLTIRREGAGYHDEAGSGSIASATAIRRMLEQGGGAAGIARYVPASTLRVVEEQLAAGEAPRRWDDYFPQLLHRLLVEPPASLAGTLGFGEGLERRIAAQLAALPELGFEPLLAAVKTKRYTRTRLQRALLGVLLNLRAAELGRERLAAGPGYIRVLGFTPRGQQLLARMRREASAPVLTSAARADGLPLLELDVRGTAVHAAGGGSRDPRRLLRDYYEPPIRL
>NZ_CP045802.1|WP_153783739.1|3380272_3380776_-|DUF177-domain-containing-protein
MEFRVMEVVSKGQEPSFREKLDVTELLQDRKDVVAAKPMSVELDVRPYEGTAQVAGELRADLTMVCSRCLEPVEEHLSIPIEERFALASMVKDPEADEDLILVAEDKVDLQPYVEGTLLIYLPMAPLCSDDCKGLCPDCGTNLNEQSCGCSRDVIDPRFEALKKLLE
>NZ_CP045802.1|WP_028597468.1|3380048_3380222_-|50S-ribosomal-protein-L32
MAVPQRRTSKTRRDKRRTHFKLTVPGMVKCEQCGELKLAHHVCKVCGYYKTKEVISQ
>NZ_CP045802.1|WP_028597467.1|3379298_3379904_-|transcription-factor-FapR
MVQVIERLPKKQRHQQLLKHMEDNPFMTDRELTRLLKVSIQTVRLDRMELGIPELRERLKLMAERSYDPIRSLQADEVIGEIVDLQLDRSGISIFEIGEEHAFSRSGIARGHHLFAQANSLAVAVINDEVALTATADIRFLRPVRLGEKCIAKAYVRRAGQRSKAKVEVFSYVGDELVFEGQFMIHRSGGEAASIEGGDEH
>NZ_CP045802.1|WP_028597466.1|3378300_3379302_-|phosphate-acyltransferase-PlsX
MKIAIDAMGGDRAPAEIVKGALAAAREWPDTQLVLVGAPEAIEAHLDGAPPSNLTIHPASEKIEADDEPVRAVRRKKDASMVVAGRLVREGAADAMLSAGNTGALMTAGLLVVGRMDGIERPALAPVLPTLDNVGVLALDLGANMDAKPEHLAQYAVMGSIYREKVHGIARPRVGLLNVGTEPGKGSELTKAAFELLEKAPIEFVGNVESRDVMQRNCDVLVCDGFAGNILLKTMEGTAGAIMKELKSAFTSSLLTKLAAAVLMPGLKGLKSKMDYAQYGGAPLLGLNGLVVKCHGSSDAESVKNAVRQARIALQARLIPTVAAEIKGKEVLS
>NZ_CP045802.1|WP_153783745.1|3389129_3389756_-|ATP-binding-cassette-domain-containing-protein
MLEVDKVGIHLGGRWLFRDMSLTLEAGEVVGISGDSGVGKSTLARMLAGHLAPDEGEVRYGGRPAARRGPHPAQLVLQHPERAVNPRWRIRRILAEAGAPEPSLLEALQIAPSWLDRWPSELSGGELQRVCIARALGPATRVLIADEMTAMLDALTQAGIWRAALGVAQERGLGVLAISHDEALLERICTRRLRWEELRGDATTVMMP
>NZ_CP045802.1|WP_153783746.1|3389979_3390987_-|ATP-binding-cassette-domain-containing-protein
MAIGAKRVPAQEASLRGASSEEAALGAAAPLLEIEGLRVSFLQYGRGLQRRTVQALAGVDLSVGAGELVALVGSSGSGKSLLAHAVMGLLPDNARSSGSIRYAGEPLDGERLLRLRGKELALVPQGVTYLDPLLRAGEQALGRQRGPQARSRLRAVFSRFGLPERAERLYPHQLSGGMARKVLVSAAALGGARLVVADEPTPGMEAGKAAEALQALRELADGGCGVLLLTHDIEAALRVADRVAVLYAGEAVELAAASDFAGAGERLRHPYTRALWQALPANGFRPLPGVQPAPEEAAASCAFAARCGQAAPECRAAKPAMRAWRGGQVRCFKPD
>NZ_CP045802.1|WP_153784743.1|3391040_3391904_-|ABC-transporter-permease-subunit
MQAASQRKAVPAASLPSGRLRLLVGAALLVAALLGLGLWASLSGGGEGLRTNLAERSLPPSWGHPLGTDWLGRDMLVRTVQGLWLSLQVGLLASLAGAAIAAAAGLSAALLGRTADRIVSWLMDLFLSLPHLVTLILIAFVCGGGLRGVLIGVALTHWPSLARLIRAEAMQLRSADYVAVSRSLGKSRVWIMTRHLLPHLLPHLLTGCLLLFPHAILHEAAITFIGLGLPPDQPAIGVILSESMRYLNAGLWWLAVFPGVALLLLVGAFDRLGHAASALLDPGRSQQ
>NZ_CP045802.1|WP_153783747.1|3391918_3392998_-|ABC-transporter-permease-subunit
MEKLSADIQDGRRRGAGAEAAQSASGGEGIKGGWGLYLLGKALRLVLLLAAVSAVTFTLVSHSPVDPVRAYIGADILRVGPEQQAQIASYWGLDEPPLERFFRWVGALLSGDLGTSMIYREPVADVIAERFASSALLMAAAWLLSGALGFSAGIAAAMAHGRWPDRLIRRCCYLLASTPPFWLALLLLTVFGVALGWFPIGLAAPAGMAAEEVGWLDRLRHMALPALTLSVVGIAPVVLHTRQKLLEVLASDHVLYARSRGERGWALLRRHGLRAVALPALTLQLAGFSELFGGAVLAEQVFSYPGLGQATVQAGLRGDVPLLMGLVLGSALFVFAGNLLADLSYRLVDPRLRERSRTS
>NZ_CP045802.1|WP_153783748.1|3392985_3394701_-|ABC-transporter-substrate-binding-protein
MRHDRGRQDVRNGSGAGFRREKRRKLRPAVAAALIAVALAGCAGAEGTPAPSAKPAGAGAEADGNAGQAAAQAKDSLILAVGSEPETGFDPVTGWGRYGSPLFQSTLLKRDDDLNIVNDLATGYEVSGDGLEWTVKLRGDAVFTDGVPVTAEDVAFTFEQTAKSGAAVDLTNFEAVEAPAVDVVVFRLHSPQSTFVSLLVSTGIVPKHAYGPSYAEQPIGSGPFQLVQWDKGQQLIVEANPDYYGRKPSFKRLTFLFLGEDAAFAAAKAGEADVAYIPSSFSRQPVAGMTLVDVKSVDNRGIQFPYKPAGGKTSGGDPIGNDVTSDPAIRKAVNAAIDRQALVDGVLDGYGSPAYSPSDGLPWWNPDTTVPDGDPAAARQLLEQGGWSDPDGDGILDKDGQRAEFTLLYPAGDVTRQSLALAAADMVRAAGIEIRPDGKSWEEIEKRMHADATLFGWGSHDPLEMDHLFRGASGGVGYYNAGYYANKTVDAWMDKALAAPSETEALEFWKKAQWDGETGFSALGDAPWAWLVNLDHLYLVSDKLDVGKQRIQPHGHGWPITDNIADWTWKS
>NZ_CP045802.1|WP_028596831.1|3394975_3395392_-|nickel-responsive-transcriptional-regulator-NikR
MAEKEELVRFGVAFPAPLIERFDGYIEAKGYTNRSEAIRDMARKAMLEDEGIAPETAVAGTISLVYDHHVRELPLLLTELQHDYHEEIISTMHVHLTHHQCMEIILIRGRVERLRRLHGAIQAQKGVQVAEMSVTFLE
>NZ_CP045802.1|WP_153784744.1|3395653_3396919_-|extracellular-solute-binding-protein
MTASLLILLMMGGTLSACSGVKEEEAGTADGGGATVKLRIMWWGSQARHDATLKALDAYASANPGVAFEPEYQSFDGYQDKLSTMSAGKNTPDLFQMDAAWFNDWASSGRLEDLSSIPAADIDTSLLETGTYEGKLYAMPLGNNAWGMIYNKTMMDSLGVAPPTTWDEFFQLARDIKPKLAKDQYLSKDLTADGAMYMSYQLSMGKGYSLSKDGKFHYDEATWKDWMNKWAVLRQDKLAAPPDVTVSDKGQDAQMDLLVQKKILLKGAHAAEFGGFDALMPGDLALTALPRGAQASGWLKASMYWSVSPNSKHKEEAKKFIDWFVNSEEAAAILGTSRGIPVSRTVVEAIQQNFTAVDKNALGLIETVSKDGSAFDPGPGNKGGWANFTKEYDNIVQSILFGKIGIDEGWEQVVGLSRNLG
>NZ_CP045802.1|WP_153783749.1|3397050_3398673_-|response-regulator
MWTIAIVDDDRQALDGMSRLIPWDQLDASLVGEASDGEQGLRLIEEKNPDIVITDIYMPVMNGLDMIEELRKQKYGGKIIILSGYSDFDYARKALRLSVDDYLPKPASLPTIREVLGRVAAELSRQKAVESEERKIREKLLQYEPYWEREWAKSVLTGGVPSPSGTAAELPAKLGWSRAQVMTLAVELKRQGRMEGMSLRDWSLFRFAIGNMVEELAAAAGMRSLFLELHSHQMAILLSKPLSWPEPVFRQEALELAGRIVDAAGSCLHVKLRIGAGSRKSDWRLAADSTEEAFRALGSRRQPHPLHPCVYLHEEGSGSPGSSRELRPVRFFQEMADAIRSFDERRALLALEQFCREGGGAASSLDEAMLEEIGAQLFAILSFTLYESGIRLDDALAPSELSRELALVEGVSSWKDWVAEKIRLVCSRYAPNENLKHKETVDFIIQYIHEHYAENIHLQQLADRVYISKNHLSTIFRQATGETFGDYLTRVRMERAKSMVLEKRLLVAEIAERVGYRNVPYFTTLFKRHTGKSPTEFYKA
>NZ_CP045802.1|WP_153783750.1|3398647_3400432_-|HAMP-domain-containing-protein
MNPFRKHRVDKVFLLSFAAFIGLLVTVIMAVSYQLSAREQATSASAYQQAMLQQLNKQLTDQMDAVEQTALFISLNAQLASYLTSKGDYFALKKARDELNRDYLAPILNSSRSIFTFQVYMNEPLQVDPNAAIQYLPLSQARSESWHAAVEKADSVWVGQRAVGSPQGEQQAVSFIRRINTPEGVNLGLLVLNVRMRFLQSILTEDNSSASRLLLDSGGRMIMHANRALPPGEIEALQQQVRGDAGHARQRLAAAGSQPAKDMLTVWSRTTPNSWMLVELTPWKEITGGSVRLAWTLAGVGAAAILLALVFTLYLSRSFTRPIRQLVQLMKSYAPGRPARPPQTEYRNEFGSLFGGYRKLTERIEGLYQSLEQQHRAQRRAEIRALQAAINPHFLYNTLDQLNWMAIEAGQEKISHVVELMGRMFRISLSGGETMIPLQEELLLVESYLGIQQAKWRSGLEYRIEIAGELRELLVPKLTLQPFVENAIVHGFHGSSRGLVTISGEQHGSGMRLVVQDDGIGLRDDWQARKRTRTGGYGVRNVKERIEVLFGRPYGVELRSLPERKGTRVEIYLPSREDHGAERGEPHVDDRDRG
>NZ_CP045802.1|WP_153783751.1|3400541_3401378_-|ABC-transporter-permease-subunit
MNGKPRKSNLLVHLVMIAACLVMSYPLLWWIGASFKSAAELGNPGLFPEQWLWRNYSDGWVALPQYTFTRFFENSLLLNASTTLLHVVSASLVAFGFARLTFPLKGMWFSILLLTLMLPGQVTLIPQYTMFHAFDWINTYLPLIVPSAMGGAFFIFLLVQFIRGIPRELDESAKIDGCSWFGIYARIVMPLTVPALITVMIFSFIWGWDDYFGPLIYLNTVDKYTVPLALRMFIDTQSAVAWGQLLAMSLLSVLPPVLIFFLAQKHFVEGIATSGLKG

Crispr_ID: NZ_CP045802_17

• CRISPR_ID: NZ_CP045802_17
• CRISPR_location: 3884675-3884750
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_17

Consensus_repeat	Method
CAGTGGTACTTTTACCACTGACG	CRISPRCasFinder

spacers of NZ_CP045802_17

>17.1|3884698|30|NZ_CP045802|CRISPRCasFinder
GGCGCCATTTCCGCCGCAGAGCCTGCACGT

CRISPR arrays and Neighbor proteins around NZ_CP045802_17

CRISPR arrays

The CRISPR arrays of NZ_CP045802_17

>merge|NZ_CP045802|17|3884675-3884750|CRISPRCasFinder
CAGTGGTACTTTTACCACTGACGGGCGCCATTTCCGCCGCAGAGCCTGCACGTCAGTGGTACTTTTACCACTGACG

>NZ_CP045802|17|14|3884675-3884750|CRISPRCasFinder
CAGTGGTACTTTTACCACTGACG	GGCGCCATTTCCGCCGCAGAGCCTGCACGT
CAGTGGTACTTTTACCACTGACG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_101807834.1|3886438_3887443_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|236863
NZ_CP045802.1|WP_101807832.1|3882794_3884267_+|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|225307
NZ_CP045802.1|WP_101807838.1|3894551_3894947_+|VOC-family-protein	unknown	unknown	gnl|CDD|319910
NZ_CP045802.1|WP_052332873.1|3873438_3875706_-|transglutaminase-domain-containing-protein	unknown	unknown	gnl|CDD|376628
NZ_CP045802.1|WP_028597171.1|3891523_3891907_-|MerR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|133384
NZ_CP045802.1|WP_028597175.1|3893057_3894161_-|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_CP045802.1|WP_028597167.1|3885746_3886406_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|224922
NZ_CP045802.1|WP_153783896.1|3891912_3892893_-|aldo/keto-reductase	unknown	unknown	gnl|CDD|381305
NZ_CP045802.1|WP_043110746.1|3875692_3876976_-|DUF58-domain-containing-protein	unknown	unknown	gnl|CDD|224635
NZ_CP045802.1|WP_153783893.1|3880327_3881605_+|MFS-transporter	unknown	unknown	gnl|CDD|340897
NZ_CP045802.1|WP_052332875.1|3881803_3882373_+|NlpC/P60-family-protein	unknown	unknown	gnl|CDD|366353
NZ_CP045802.1|WP_028597166.1|3884847_3885696_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270315
NZ_CP045802.1|WP_153783894.1|3888625_3890605_+|copper-amine-oxidase-N-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|377924
NZ_CP045802.1|WP_153783895.1|3890629_3891403_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028597159.1|3872671_3873199_-|YqeG-family-HAD-IIIA-type-phosphatase	unknown	unknown	gnl|CDD|225090
NZ_CP045802.1|WP_028597162.1|3878464_3879484_-|stage-V-sporulation-protein-AD	unknown	unknown	gnl|CDD|183504
NZ_CP045802.1|WP_043110818.1|3879485_3879938_-|stage-V-sporulation-protein-AC	unknown	unknown	gnl|CDD|131885
NZ_CP045802.1|WP_052332874.1|3876978_3877935_-|MoxR-family-ATPase	unknown	unknown	gnl|CDD|223786
NZ_CP045802.1|WP_101807835.1|3887738_3888497_+|YdcF-family-protein	unknown	unknown	gnl|CDD|99750
NZ_CP045802.1|WP_028597161.1|3878117_3878468_-|stage-V-sporulation-protein-AE	unknown	unknown	gnl|CDD|131886

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_101807834.1|3886438_3887443_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|236863	PRK11153, metN, DL-methionine transporter ATP-binding subunit; Provisional.	0
NZ_CP045802.1|WP_101807832.1|3882794_3884267_+|NAD(P)/FAD-dependent-oxidoreductase	gnl|CDD|225307	COG2509, COG2509, Uncharacterized FAD-dependent dehydrogenases [General function prediction only].	1.95538e-179
NZ_CP045802.1|WP_101807838.1|3894551_3894947_+|VOC-family-protein	gnl|CDD|319910	cd07246, VOC_like, uncharacterized subfamily of vicinal oxygen chelate (VOC) family. 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.	1.54324e-37
NZ_CP045802.1|WP_052332873.1|3873438_3875706_-|transglutaminase-domain-containing-protein	gnl|CDD|376628	pfam01841, Transglut_core, Transglutaminase-like superfamily. This family includes animal transglutaminases and other bacterial proteins of unknown function. Sequence conservation in this superfamily primarily involves three motifs that centre around conserved cysteine, histidine, and aspartate residues that form the catalytic triad in the structurally characterized transglutaminase, the human blood clotting factor XIIIa'. On the basis of the experimentally demonstrated activity of the Methanobacterium phage pseudomurein endoisopeptidase, it is proposed that many, if not all, microbial homologs of the transglutaminases are proteases and that the eukaryotic transglutaminases have evolved from an ancestral protease.	9.14442e-26
NZ_CP045802.1|WP_028597171.1|3891523_3891907_-|MerR-family-transcriptional-regulator	gnl|CDD|133384	cd01109, HTH_YyaN, Helix-Turn-Helix DNA binding domain of the MerR-like transcription regulators YyaN and YraB. Putative helix-turn-helix (HTH) MerR-like transcription regulators of Bacillus subtilis, YyaN and YraB, and related proteins; N-terminal domain. Based on sequence similarity, these proteins are predicted to function as transcription regulators that mediate responses to stress in eubacteria. They belong to the MerR superfamily of transcription regulators that promote transcription of various stress regulons by reconfiguring the operator sequence located between the -35 and -10 promoter elements. A typical MerR regulator is comprised of distinct domains that harbor the regulatory (effector-binding) site and the active (DNA-binding) site. Their N-terminal domains are homologous and contain a DNA-binding winged HTH motif, while the C-terminal domains are often dissimilar and bind specific coactivator molecules such as metal ions, drugs, and organic substrates.	1.54392e-50
NZ_CP045802.1|WP_028597175.1|3893057_3894161_-|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	2.48415e-85
NZ_CP045802.1|WP_028597167.1|3885746_3886406_-|ABC-transporter-permease	gnl|CDD|224922	COG2011, AbcD, ABC-type metal ion transport system, permease component [Inorganic ion transport and metabolism].	3.59501e-101
NZ_CP045802.1|WP_153783896.1|3891912_3892893_-|aldo/keto-reductase	gnl|CDD|381305	cd19079, AKR_EcYajO-like, Escherichia coli YajO and similar proteins. Escherichia coli YajO is the prototype of this family. It is an uncharacterized aldo/keto reductase family oxidoreductase.	0
NZ_CP045802.1|WP_043110746.1|3875692_3876976_-|DUF58-domain-containing-protein	gnl|CDD|224635	COG1721, COG1721, Uncharacterized conserved protein (some members contain a von Willebrand factor type A (vWA) domain) [General function prediction only].	8.8619e-32
NZ_CP045802.1|WP_153783893.1|3880327_3881605_+|MFS-transporter	gnl|CDD|340897	cd17339, MFS_NIMT_CynX_like, 2-nitroimidazole and cyanate transporters and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Escherichia coli 2-nitroimidazole transporter (NIMT) and cyanate transport protein CynX, and similar proteins. NIMT, also called YeaN, confers resistance to 2-nitroimidazole, the antibacterial and antifungal antibiotic, by mediating the active efflux of this compound. CynX is part of an active transport system that transports exogenous cyanate into E. coli cells. The NIMT/CynX-like 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.	1.04709e-132
NZ_CP045802.1|WP_052332875.1|3881803_3882373_+|NlpC/P60-family-protein	gnl|CDD|366353	pfam00877, NLPC_P60, NlpC/P60 family. The function of this domain is unknown. It is found in several lipoproteins.	5.60999e-27
NZ_CP045802.1|WP_028597166.1|3884847_3885696_-|ABC-transporter-substrate-binding-protein	gnl|CDD|270315	cd13597, PBP2_lipoprotein_Tp32, The substrate-binding domain of the 32-kilodalton lipoprotein (Tp32) from Treponema pallidum binds L-methionine; the type 2 periplasmic-binding protein fold. This group includes the lipoprotein Tp32, a periplasmic component of a methionine uptake transporter system, and its closely related homologs. The Tp32 has both structural and sequential homology to the MetQ family of substrate-binding protein, and thus it belongs to the type 2 periplasmic binding fold protein superfamily (PBP2). The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea.	6.46262e-130
NZ_CP045802.1|WP_153783894.1|3888625_3890605_+|copper-amine-oxidase-N-terminal-domain-containing-protein	gnl|CDD|377924	pfam07833, Cu_amine_oxidN1, Copper amine oxidase N-terminal domain. Copper amine oxidases catalyze the oxidative deamination of primary amines to the corresponding aldehydes, while reducing molecular oxygen to hydrogen peroxide. These enzymes are dimers of identical subunits, each comprising four domains. The N-terminal domain, which is absent in some amine oxidases, consists of a five-stranded antiparallel beta sheet twisted around an alpha helix. The D1 domains from the two subunits comprise the 'stalk' of the mushroom-shaped dimer, and interact with each other but do not pack tightly against each other.	6.35596e-07
NZ_CP045802.1|WP_028597159.1|3872671_3873199_-|YqeG-family-HAD-IIIA-type-phosphatase	gnl|CDD|225090	COG2179, COG2179, Predicted hydrolase of the HAD superfamily [General function prediction only].	4.91497e-62
NZ_CP045802.1|WP_028597162.1|3878464_3879484_-|stage-V-sporulation-protein-AD	gnl|CDD|183504	PRK12404, PRK12404, stage V sporulation protein AD; Provisional.	0
NZ_CP045802.1|WP_043110818.1|3879485_3879938_-|stage-V-sporulation-protein-AC	gnl|CDD|131885	TIGR02838, stage_V_sporulation_protein_AC, stage V sporulation protein AC. This model describes stage V sporulation protein AC, a paralog of stage V sporulation protein AE. Both are proteins found to present in a species if and only if that species is one of the Firmicutes capable of endospore formation, as of the time of the publication of the genome of Carboxydothermus hydrogenoformans. Mutants in spoVAC have a stage V sproulation defect. [Cellular processes, Sporulation and germination].	4.62525e-64
NZ_CP045802.1|WP_052332874.1|3876978_3877935_-|MoxR-family-ATPase	gnl|CDD|223786	COG0714, COG0714, MoxR-like ATPases [General function prediction only].	5.51939e-96
NZ_CP045802.1|WP_101807835.1|3887738_3888497_+|YdcF-family-protein	gnl|CDD|99750	cd06259, YdcF-like, YdcF-like. YdcF-like is a large family of mainly bacterial proteins, with a few members found in fungi, plants, and archaea. Escherichia coli YdcF has been shown to bind S-adenosyl-L-methionine (AdoMet), but a biochemical function has not been idenitified. The family also includes Escherichia coli sanA and Salmonella typhimurium sfiX, which are involved in vancomycin resistance; sfiX may also be involved in murein synthesis.	4.49473e-36
NZ_CP045802.1|WP_028597161.1|3878117_3878468_-|stage-V-sporulation-protein-AE	gnl|CDD|131886	TIGR02839, stage_V_sporulation_protein_AE, stage V sporulation protein AE. This model describes stage V sporulation protein AE, a paralog of stage V sporulation protein AC. Both are proteins found to present in a species if and only if that species is one of the Firmicutes capable of endospore formation, as of the time of the publication of the genome of Carboxydothermus hydrogenoformans. Mutants in spoVAE have a stage V sproulation defect. [Cellular processes, Sporulation and germination].	3.12845e-44

Protein sequences

>NZ_CP045802.1|WP_101807832.1|3882794_3884267_+|NAD(P)/FAD-dependent-oxidoreductase
MGKYDVIVVGAGPAGIFACYELTLKAPQLKVLLVDKGHSIDRRSCPILEEKIQLCPPPAGKKEFAGCLPACSITAGFGGAGAYSDGKFNITTEFGGWLTDYLPPSQVLELIRYVDRINLEHGATTAITDPTTDTIRDIEQRGYAAGLKLLRAEVRHLGTEQNLAILKSIFDYLQTRVDMRFKTEVEDLVTVKENGAHRVTGITIRGGETHEADVVMVAPGRDGSAWLTEVLKRRRLKMHNNQVDVGVRVETSDVVMREINEHLYEGKFIYNTSVGTRVRTFCSNPSGHVVVENHSGVMAANGHSYKDPALGSSNTNFALLVSHRFTEPFDKPNEYAREICQRANDLSSGGVIVQKYGDILRGRRSTASRIREGFLEPTLHEAVPGDLGLVLPYNTMRSLIEMVEALEKVTPGIASEHTLFYGVEAKFYSARPKLTNDLETEISGLYCGGDGAGITRGLAQAGAAGVWIARAMLRRTSGSAAGAEAALPTL
>NZ_CP045802.1|WP_052332875.1|3881803_3882373_+|NlpC/P60-family-protein
MNHHHHPMLRRLLVVTAAATLVAGLSLPSTAAASTAAVSSVSTSAASASADDAAASVSASSKADRIIAFAQSLRGKVKYVYGANQPSRLVFDCSSFTKYVFASEGVSLKWGSTAQSKQGVKVGKDSLRKGDLMFFRSSSGSSSKISHVGIYIGDGKFIHNTIGSNVNGVVISSFNSSYQKRFVSAARVL
>NZ_CP045802.1|WP_153783893.1|3880327_3881605_+|MFS-transporter
MSERRALSMIPHSSPAGRRPTWLAVAGILLIAANMRAAITSVGPLLDRIATDYRLSSEMSGLLTSLPLLAFGAMSLLAPRLAEKLGSERSLLYGLALLLAGMLIRALPGTEALFAGTALLGLAIAVSNVLLPSLIKRDFPGQIGLLTGSYSVTMSVFAAIASGASVPLAALPGWDWSRSLLLWALLAALAFAVWLPVSLSSKRVAAAAPAQSPARMLRSPLAWRITLYMGLQSLTFYATITWLPVLFHERGFSAASAGWLLSLMQLVSLPTSFFVPVWASRMRSQVPLVGIAGALSLSGYAGLLWGSASMSLLWITLLGLSQGATISLALTFFGLRTRTAAEAARLSGMAQSIGYFLAAFGPVLLGTLHDRTGSWNPVLAVLLLVSVVVVALGLGAGRPGTISEPHGGASGLRSPAGGKLTGPAR
>NZ_CP045802.1|WP_043110818.1|3879485_3879938_-|stage-V-sporulation-protein-AC
MTMSPKEYKAFAKNREPARSVLGNCIRAFLVGGFICLIGQGVQEFFMHAFGFDAEKAANPTVAVMILLSIILTCLGVYDKIAQWAGAGTAVPVTGFANSMCSAALEHRSEGLVLGVGANMFKLAGSVIVFGTVAAFFVGIAHLILGTGGQ
>NZ_CP045802.1|WP_028597162.1|3878464_3879484_-|stage-V-sporulation-protein-AD
MKKGKQTWWFENRPVIIGTATVVGPDEGDGPLAADFDLVHPELDLQQKSWEKAERLLLEQASDLAIKKSGIAKDELEFYVGGDLMNQIISNTFAARTLGVPYLGVFGACSTSMESLAIASMIVNSGNGTHVLAGTCSHNCTAEKQFRYPTEYGSQKPPTAQYTITGAGAAIVAPAGSGPVVECATIGRIVDLGVKDPFNMGAAMAPAAVDTIQAHLTDTGRSPGDYDMIVTGDLATVGHRIATDLLKRGGVPMEETVFADCGLMVYDVDRQKVQAGGSGCACSAVVTYGHLLKRIEKGELRRILVVATGALLSPLSFQQGESIPCIAHAVSIERNEVKP
>NZ_CP045802.1|WP_028597161.1|3878117_3878468_-|stage-V-sporulation-protein-AE
MIYLWAFVIGGAICVFGQLLFDVVKLTPAHTMSLLVVLGAIVDGLGWYEPLIKFAGAGVTVPITSFGNSLVHGALTELHDTGWIGVISGIFKVTSAGISAAIIFSFLAALIVRPKG
>NZ_CP045802.1|WP_052332874.1|3876978_3877935_-|MoxR-family-ATPase
MEVYAPHTRLCSSIRSNLESVILGKEREIELVLIALLAGGHLLLEDVPGTGKTQLVKALARSIGGDFRRIQCNPDLLPTDITGLTIYHPREEQFIFRPGPIMSHLVLADEINRATTKTQSALLEAMEENSVTVDGETHALPAPFILIATQNPIEFEGTYLLPEAQMDRFMMKLSLGYPGEADEKRMVLGRQSGHPVDALERVASIADIIALQQQAERIHADEAVADYLVRIVRGTREHEGVQLGASPRAAVALMRAAKARALVEQREYVIPDDVKQLSPHVLSHRLLLQPSARLRGTRPETVVQDVIERTKAPVRLER
>NZ_CP045802.1|WP_043110746.1|3875692_3876976_-|DUF58-domain-containing-protein
MRRPATDRRSVRARRRWGLMASLYVSSLLYMLFQGGKTAVMLFCIFNGLILYLILGYWSGIRRISGSRRIAATAPAGMAAGSADSRVLAAGDSLRVEMQLRLPGYYPVPYVLVQERLERNGGETIPFEVSFVPGMRRSGAADFETPPLRRGVYRFLPTLCTTKDVFGFLEHEGSFEEEMSFSVRPRTIAVPGWDRVSRGAKGHFSHSAAPRSSRETTQINGIREFIPGDRLSRIHWGATAKTGQWKSKEFEREALPRTIVLLDACVRSGPGEAERFETAVSAAASLFEHGMKRGTSMGLWCSSAVPAALKARSGGDQLHRAMELLTEASRDGADRLAQAVLRADPILEAGSMTLLVTDAPPEEIRQAMSWLARRGHNPCCIRVLDEDQARSADGLSDHAVGPVHAIRSLEELPEALSGREAAADAGS
>NZ_CP045802.1|WP_052332873.1|3873438_3875706_-|transglutaminase-domain-containing-protein
MLEAEPTRGRMRTSRGWERLQPPARARWFLALSGVLTAVMIASSLSVLEELWWEETYTIVYAVLGVAALLELLPVRRLLRLVLQAVAVAVILVQLAPVDWSLLPRPAEIGLGESVRAAATLLHPFWEIALAVWAVHAMFAAWNRARIRIVGFTTVNLLVLAISDSFTPIYLWDSVAIVVFAGLVWLIAEHYAGFQQRHPVSWRRLLRYPLQLLLPIVLVLSLVMAAGLAAPEIPPLLKDPYTAWQESRGVAVQNFVGDKGIAPASSKKSAKSGYSRDDSKLGGGFNFDYSPVMEVSSTHKSYWRGETKDYYSGEGWKASEAISSPFELPLGTDLGDRPDIAGAETVMVDQTFTMLRKDKFPVLFAAPSVRSLKPPEREDGSRMRVLYDSRTEKLMPDPGGNAYPSSYTIRSEQVVLSEELKAAPAIMETGMISDYYRQVPSKTPSRVADLAREITAGAATDYDKAKAIETYLSTTFPYTNEPDLTKKKSADFVDSFLFEIQEGYCDYFSSAMAVLARSAGLPSRWVKGYASGTGTVDPEAMMRGGREAAERMDRDGADTYTVRNSDAHSWVEIYFEGYGWIPFEPTPGFAFPYASAAAEAAPEPSLAPEPSAAPDATEAPAEAAGPLVPRWLGWTGLGLFAAAAAVLAFLRRDWLAARWRGYRTRSLTAEQRIVWETERLIRSARRHGLAKAEHETLREAVERWSGQRRFLKQELGEVLGLFERTKYGGRPATREEADSYAAKVRELSGRLRSPG
>NZ_CP045802.1|WP_028597159.1|3872671_3873199_-|YqeG-family-HAD-IIIA-type-phosphatase
MFERLVPHMRVKSIYDIDLDLLARKGVKGIITDLDNTLVGSKIALATPELIVWLDRVRELGFQVVVVSNNHETRVSRFALPLSIPFIHAARKPSTRAFRKALVVLGLEAEQTVVIGDQMMTDVLGGKRMGLYTILVSPIAPLDEGFGTRINRLLERIALTRLRRKGLWQEEETGK
>NZ_CP045802.1|WP_028597166.1|3884847_3885696_-|ABC-transporter-substrate-binding-protein
MNKWLKGITVAALAVSLAACGAKNEGNNAPADNAANSGGAAAEPVTLTVGATAVPHAEILNHVKDQLAKEGVDLVVKEFTEYVQPNVQLYEKQLDANFFQHVPYLDDQNKERGYDLVKVVNVHVEPMGAYSDKIKSVDELQDGATVAIPNDATNGGRALALLAENGLITLKEGVGIAATVKDVTENAKNLKFKELEAATLPRVLGEVDLAVINTNYALEADLNPTADALFIESKDSPYANILVARPDNKDSEAIQKLAKALNSEEVKTFIDETYKGAIVAAF
>NZ_CP045802.1|WP_028597167.1|3885746_3886406_-|ABC-transporter-permease
MDWSRIDPAEIWTATQDTLSMLGLSLVFTIALGLVIGVLLYLTSSRQLLYLPVVYSFLSLVVNILRSVPFIILMIAVMPLTKEIAGTTIGVAGTIPPLVIGAAPFFGRLVETALREIDRGIIEAAQAMGASKWDIVRRVLLRESRPGLLAAVTVTAITLVSYTAMAGVVGGGGLGDLAIRYGYQRYQTEVMIVAVVVLILLVQLLQMLGDWLVRKISRK
>NZ_CP045802.1|WP_101807834.1|3886438_3887443_-|ATP-binding-cassette-domain-containing-protein
MIELQHVTKIYKGRGGTVDAVKDVSLKVEPGEIYGIIGHSGAGKSSLIRCMNLLERPSSGKVLFGGRELTSLKERELQAERRRIGMIFQHFNLLTSATVRENIAFPLVLAGQSKRRQAARVDELLELVGLQAHGDKYPAQLSGGQKQRVGIARALAAEPAVLLCDEATSALDPQTTSSILSLLLSINEKLGLTIILITHEMQVIRSICDRVAVMDAGRVVEEGPVLDVFLRPAHGVTKQFADELSELEGGAPLPRRAGSKLVRLHFVGEETYEPVLFEAVKDSAVQCAILQGTVSRMKHTPYGQLLVELSGSPSDIDGAIASLRSSGIDAEVLP
>NZ_CP045802.1|WP_101807835.1|3887738_3888497_+|YdcF-family-protein
MIYFIKAIYSFLLPPGLFLLLLGAASWRMLRRDRRWAMLPLAALLLLYALSSPWAADGLARSLEQRYPQPALNETASDVIVVLGAGAVPDTPDVGGLGNMSATAEARLLAAVRLSRSTGLPVLFSGGQVYPDSGNEADIAGRQLRELGLPPDRILLENRSLNTEQNARLTRRLLYERGLSRPMLLTSALHLPRALEQFRKAGLEPLPYPVDYAAPVQPRWYWSKLLPSGAALALSQAALKEHLGLAALKLGL
>NZ_CP045802.1|WP_153783894.1|3888625_3890605_+|copper-amine-oxidase-N-terminal-domain-containing-protein
MKWWKSLALLSLAAAPLYGAAGEASAEPGVNTITLTKGSKQMDKDGTAITAVQPLTIKNDVSYAAFSTLAQLYGYKTSYDAKAKESIAKTPSGEIRFRMNTKDIWVDGTKWTGEAASYSEKGSLMIPIRTWAKISGSSISFSGKQILLRWTEQQAPTAGFQVQPAVIYAGDPVTYVDQYASPSGAPLLNEEWTGRQDVFVEPGTYTVTRRAQDADGNWSEPFTVTVQVLAVNQPPVADFTTDKPVYRQGEKIAYTDLSSDDNNAIDPAKTKWTGKQDAFFSPGDHTVTLSVTDAQGLTSTVSKTISVTDEILYTENEFGLLFAQPGEKIRVDGDQVLNIPTRSYDFDSEPSKMIRSNSPEIWNEEGIVFDDQFDGKVRLLFHNKNNMSGNVPGNVRMYLAVTNEGYQTARFGVGATGTGGPDPSEIRTGKLSTIRYLTAVNANGPQTYTDIKAGETKLVLNEISQNAIKPGMVYSAYADVTADRTLRFRVVVVRDGREPIAALDQLSLLPADGTHTRGSFNNTTRDIHIDGMLGEGGKAERVVLGDNKLDPYLDGYDNSDGSLQLNRGNFGVLYKMTVTLAPRTVIYLNPRGGLYAGAFIVNGQIVPVTNNEQLKNSSEAAVLHRSGDSPETVELKYMIASGSNLPITMVFQPMPPLKS
>NZ_CP045802.1|WP_153783895.1|3890629_3891403_+|hypothetical-protein
MTLKWRDEYEPEHPEDVRASRRKRWIRDAVLGLLLLAVCVLAAKHFSARVFELDGTLYKLESAAGETRRYAPVTGSAAGAVVAAGSDTERVVTAGGYQFRIEELVAEAGKPPAMADAVFRIAYPGGETYRVEWSQGLLLAYDAEGEFYAGAAAYANGAPVGGGTVPERFHPAAVLTAAYPDFQESRGQPIPFGLAVLLFVLGWGMLRFERVRRAFYWLSLDWLRREDPDPESGELSYYKLSGIAVMVGGVLLGLASL
>NZ_CP045802.1|WP_028597171.1|3891523_3891907_-|MerR-family-transcriptional-regulator
MTISEVSERFGLSQDTLRYYERIGLIPPVRRSASGIRDYGEEDLKWIDFVKCMRQKAGLPVEMLIEYLALFQQGDGTLDARKTLLVEQRGRLAEKIDDMTSTLRRLDDKIARYEQTIGGKEQALRAP
>NZ_CP045802.1|WP_153783896.1|3891912_3892893_-|aldo/keto-reductase
MDYVKLGKTGLDVSRICLGCMGFGDATRWTHPWVLDEERSREVIRQALELGINFFDTANVYSAGTSEEYLGRALRDYANRDEVVIATKVHFRMHDGPNGAGLSRKAILSEIDKSLSRLGTDYVDLYQIHRWDYDTPIEETMEALHDVVKAGKARYIGASAMFAWQFQKALHVAEKRGWTKFVSMQNHYNLIYREEEREMLPLCREEGIGVIPYSPLAGGRLTRGRDESTLRSETDQVQKSKYDRMAEADQAIVDRLAAIAEQREAPRAQVALAWLLQQSPVSAPIVGATKAAHLETAVAALSVQLTPEEAAALEAPYVPHPVVGPQ
>NZ_CP045802.1|WP_028597175.1|3893057_3894161_-|Gfo/Idh/MocA-family-oxidoreductase
MTQTLRVGIIGCGGIANGKHLPALSQNKHVVLAAFCDIEVDKARDAAEKYGIEGAGVYADYRELLKDGSLDVIHVCTPNDSHAPISIASLEAGKHVMCEKPMAKTAAEARAMLDAAKRTGKKLTIGYNNRFRSDSQHLKKVCEAGELGDIYYARAHAIRRRAVPTWGVFLDEEKQGGGPLIDIGTHALDLTLWMMDNYKPVSVTGSVYHKLGSKENAANAWGPWDPAKFTVEDSAMGFIKMENGATITLEASWALNTLDIDEAKCSLSGTEGGADMKGGLRINGEENSRLFVKEIDLNAGGVAFYSGSSARDIDVECAAWIDAILQDKDPVVLPEQALVVTEILEAIYESARTGKTVYLNQDQPAAV
>NZ_CP045802.1|WP_101807838.1|3894551_3894947_+|VOC-family-protein
MSNAWKPKGYSSVSPYLVVPSAERAIHFLQEAFDANELRRFYRPDGSIMHVELQIEDTVVMLGEATPAWSATVAQLHLYVEDVKSAYQRAVHAGGKSIMEPTRKEGDPDRRAGVKDPAGNTWWIATQEESS

Crispr_ID: NZ_CP045802_18

• CRISPR_ID: NZ_CP045802_18
• CRISPR_location: 4125566-4125653
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_18

Consensus_repeat	Method
CCACCTATCTCGCTTCTCCAGACCGCC	CRISPRCasFinder

spacers of NZ_CP045802_18

>18.1|4125593|34|NZ_CP045802|CRISPRCasFinder
TGGGAAAGGCTCGCTTGCGCAGCGGCCTGTTCGT

CRISPR arrays and Neighbor proteins around NZ_CP045802_18

CRISPR arrays

The CRISPR arrays of NZ_CP045802_18

>merge|NZ_CP045802|18|4125566-4125653|CRISPRCasFinder
CCACCTATCTCGCTTCTCCAGACCGCCTGGGAAAGGCTCGCTTGCGCAGCGGCCTGTTCGTCCACCTATCTCGCTTCTCCAGACCGCC

>NZ_CP045802|18|15|4125566-4125653|CRISPRCasFinder
CCACCTATCTCGCTTCTCCAGACCGCC	TGGGAAAGGCTCGCTTGCGCAGCGGCCTGTTCGT
CCACCTATCTCGCTTCTCCAGACCGCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_043110899.1|4115898_4117731_-|aspartate--tRNA-ligase	unknown	unknown	gnl|CDD|234775
NZ_CP045802.1|WP_028597538.1|4112115_4113441_-|replication-associated-recombination-protein-A	unknown	unknown	gnl|CDD|237355
NZ_CP045802.1|WP_153783989.1|4126462_4128886_-|single-stranded-DNA-specific-exonuclease-RecJ	unknown	unknown	gnl|CDD|273193
NZ_CP045802.1|WP_153783986.1|4119562_4119739_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153783985.1|4114990_4115746_-|tRNA-threonylcarbamoyladenosine-dehydratase	unknown	unknown	gnl|CDD|224100
NZ_CP045802.1|WP_028597537.1|4113771_4114821_-|adenosine-deaminase	unknown	unknown	gnl|CDD|236480
NZ_CP045802.1|WP_028597529.1|4132151_4132385_-|hypothetical-protein	unknown	unknown	gnl|CDD|379375
NZ_CP045802.1|WP_153783988.1|4123737_4124997_+|IS256-family-transposase	unknown	unknown	gnl|CDD|307151
NZ_CP045802.1|WP_101807920.1|4125929_4126442_-|adenine-phosphoribosyltransferase	unknown	unknown	gnl|CDD|235028
NZ_CP045802.1|WP_153783990.1|4128948_4129845_-|cation-diffusion-facilitator-family-transporter	unknown	unknown	gnl|CDD|223131
NZ_CP045802.1|WP_153783987.1|4120312_4122490_-|RelA/SpoT-family-protein	unknown	unknown	gnl|CDD|223394
NZ_CP045802.1|WP_084136638.1|4129861_4130785_-|protein-translocase-subunit-SecF	unknown	unknown	gnl|CDD|237275
NZ_CP045802.1|WP_028597526.1|4135279_4135669_+|TIGR04086-family-membrane-protein	unknown	unknown	gnl|CDD|274969
NZ_CP045802.1|WP_028597535.1|4117770_4119021_-|histidine--tRNA-ligase	unknown	unknown	gnl|CDD|234586
NZ_CP045802.1|WP_028597534.1|4119852_4120296_-|D-tyrosyl-tRNA(Tyr)-deacylase	unknown	unknown	gnl|CDD|235383
NZ_CP045802.1|WP_028597527.1|4134293_4135079_-|DUF421-domain-containing-protein	unknown	unknown	gnl|CDD|225205
NZ_CP045802.1|WP_052332950.1|4130795_4132067_-|protein-translocase-subunit-SecD	unknown	unknown	gnl|CDD|237276
NZ_CP045802.1|WP_101808235.1|4135805_4136609_+|inositol-phosphorylceramide-synthase	unknown	unknown	gnl|CDD|239481
NZ_CP045802.1|WP_153783984.1|4110008_4111373_-|Mn(2+)-uptake-NRAMP-transporter-MntH	unknown	unknown	gnl|CDD|234815
NZ_CP045802.1|WP_153783991.1|4132659_4134246_+|stage-V-sporulation-protein-B	unknown	unknown	gnl|CDD|240529

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_043110899.1|4115898_4117731_-|aspartate--tRNA-ligase	gnl|CDD|234775	PRK00476, aspS, aspartyl-tRNA synthetase; Validated.	0
NZ_CP045802.1|WP_028597538.1|4112115_4113441_-|replication-associated-recombination-protein-A	gnl|CDD|237355	PRK13342, PRK13342, recombination factor protein RarA; Reviewed.	0
NZ_CP045802.1|WP_153783989.1|4126462_4128886_-|single-stranded-DNA-specific-exonuclease-RecJ	gnl|CDD|273193	TIGR00644, recJ, single-stranded-DNA-specific exonuclease RecJ. All proteins in this family are 5'-3' single-strand DNA exonucleases. These proteins are used in some aspects of mismatch repair, recombination, and recombinational repair. [DNA metabolism, DNA replication, recombination, and repair].	0
NZ_CP045802.1|WP_028597537.1|4113771_4114821_-|adenosine-deaminase	gnl|CDD|236480	PRK09358, PRK09358, adenosine deaminase; Provisional.	2.10278e-139
NZ_CP045802.1|WP_153783985.1|4114990_4115746_-|tRNA-threonylcarbamoyladenosine-dehydratase	gnl|CDD|224100	COG1179, COG1179, Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 1 [Coenzyme metabolism].	2.50986e-116
NZ_CP045802.1|WP_028597529.1|4132151_4132385_-|hypothetical-protein	gnl|CDD|379375	pfam13797, Post_transc_reg, Post-transcriptional regulator. This family includes post-transcriptional regulators.	4.06712e-15
NZ_CP045802.1|WP_153783988.1|4123737_4124997_+|IS256-family-transposase	gnl|CDD|307151	pfam00872, Transposase_mut, Transposase, Mutator family.	6.8439e-147
NZ_CP045802.1|WP_101807920.1|4125929_4126442_-|adenine-phosphoribosyltransferase	gnl|CDD|235028	PRK02304, PRK02304, adenine phosphoribosyltransferase; Provisional.	3.05886e-94
NZ_CP045802.1|WP_153783990.1|4128948_4129845_-|cation-diffusion-facilitator-family-transporter	gnl|CDD|223131	COG0053, MMT1, Predicted Co/Zn/Cd cation transporters [Inorganic ion transport and metabolism].	3.1273e-19
NZ_CP045802.1|WP_153783987.1|4120312_4122490_-|RelA/SpoT-family-protein	gnl|CDD|223394	COG0317, SpoT, Guanosine polyphosphate pyrophosphohydrolases/synthetases [Signal transduction mechanisms / Transcription].	0
NZ_CP045802.1|WP_084136638.1|4129861_4130785_-|protein-translocase-subunit-SecF	gnl|CDD|237275	PRK13022, secF, protein translocase subunit SecF.	1.22136e-105
NZ_CP045802.1|WP_028597526.1|4135279_4135669_+|TIGR04086-family-membrane-protein	gnl|CDD|274969	TIGR04086, hypothetical_protein, putative membrane protein, TIGR04086 family. Members of this family of strongly hydrophobic putative transmembrane protein average about 125 amino acids in length and occur mostly, but not exclusively, in the Firmicutes. Members are quite diverse in sequence. The function is unknown.	6.33549e-18
NZ_CP045802.1|WP_028597535.1|4117770_4119021_-|histidine--tRNA-ligase	gnl|CDD|234586	PRK00037, hisS, histidyl-tRNA synthetase; Reviewed.	0
NZ_CP045802.1|WP_028597534.1|4119852_4120296_-|D-tyrosyl-tRNA(Tyr)-deacylase	gnl|CDD|235383	PRK05273, PRK05273, D-tyrosyl-tRNA(Tyr) deacylase; Provisional.	8.50711e-98
NZ_CP045802.1|WP_028597527.1|4134293_4135079_-|DUF421-domain-containing-protein	gnl|CDD|225205	COG2323, COG2323, Predicted membrane protein [Function unknown].	6.88176e-70
NZ_CP045802.1|WP_052332950.1|4130795_4132067_-|protein-translocase-subunit-SecD	gnl|CDD|237276	PRK13024, PRK13024, bifunctional preprotein translocase subunit SecD/SecF; Reviewed.	1.44579e-140
NZ_CP045802.1|WP_101808235.1|4135805_4136609_+|inositol-phosphorylceramide-synthase	gnl|CDD|239481	cd03386, PAP2_Aur1_like, PAP2_like proteins, Aur1_like subfamily. Yeast Aur1p or Ipc1p is necessary for the addition of inositol phosphate to ceramide, an essential step in yeast sphingolipid synthesis, and is the target of several antifungal compounds such as aureobasidin.	5.70424e-20
NZ_CP045802.1|WP_153783984.1|4110008_4111373_-|Mn(2+)-uptake-NRAMP-transporter-MntH	gnl|CDD|234815	PRK00701, PRK00701, divalent metal cation transporter MntH.	0
NZ_CP045802.1|WP_153783991.1|4132659_4134246_+|stage-V-sporulation-protein-B	gnl|CDD|240529	cd13124, MATE_SpoVB_like, Stage V sporulation protein B, also known as Stage III sporulation protein F, and related proteins. The integral membrane protein SpoVB has been implicated in the biosynthesis of the peptidoglycan component of the spore cortex in Bacillus subtilis. This model represents a subfamily of the multidrug and toxic compound extrusion (MATE)-like proteins. Proteins from the MATE family are involved in exporting metabolites across the cell membrane and are often responsible for multidrug resistance (MDR).	2.23765e-124

Protein sequences

>NZ_CP045802.1|WP_153783988.1|4123737_4124997_+|IS256-family-transposase
MTQYQITVDQDILHQLFIGTDRDAGVARLLETVLNQVLTAQATDQLAAQTYERTSERKGYRNGSYERDVITRAGSVTLRVPRFRDGSFSTELFARYQRSEQALVLSLMEMVINGVSTRKVTKITEELCGTEFSKSTVSHLCKQLDPAVHDWNNRSLADHAFPFITIDAIYVKVREEGRICSRGVLVGYGVNEQGRREILGLRVDDTESEESWGAYFRWLKERGLHGVELVTSDYHGGLVKAIEKEFQGVSWQRCQTHFIKNVLNAAPKALQSEIKSRVRSIFDAPDMKTARSYLEQTLEAYAETAPKAMKILEDGFEDAVAVLAFPEAYRVRLRTSNGMERLNGDIRRRETVIRIFPNRASVLRLIGAMLMEENEYWMTKKPYMDMTDFKAWKKQKATQGAGSEEQETSTTMTEATDSL
>NZ_CP045802.1|WP_153783987.1|4120312_4122490_-|RelA/SpoT-family-protein
MGIDQLLAKASTYMKEQDLARIREAYVFADQAHFGQVRKSGEPYILHPVAVAEILVNMQMDVTSIIAALLHDVVEDTTVEVEQVRARFGDTCAMLVDGLTKLEKIKFRSKEEHQNENYRKMFVAMAQDIRVILIKLADRLHNMRTLKFQSEEAQRRIAYETLEIFCPIAHRLGISAIKWEMEDTALRYLNPQQYYRIANLMKKKRAEREDFIGQVISRISEKLDEMGIEGDISGRPKHIYSIYRKMTMRNKQFNEIYDLMAIRIIVDNIKDCYATLGIIHTLWKPMPGRFKDYVAMPKANMYQSLHTTVVGPNGEPTEVQIRTWEMHRTSEYGVAAHWAYKEGTAPGGNIEDKMSWFREILELQNEAEDASEFMESLKMDFFSDLVFVFTPKGEVIELPAGSVPLDFAYRIHTEVGNRTIGAKVNGRIVPLDHKLKTGDIVEILTSKHSYGPSQDWIKLTKSSHARAKIKQWFKKERREENVVKGREALERELRKLGLEPSAWMTEDKLMEAASKFSFHDPEDMMSAIGFGGITAAQICTKMTEKMRREAEAAQQIELTSEPVEMKSPGTRKKAATGGVTVKGIDNLLVRFARCCNPVPGDAIVGYITRGRGVSVHRSDCPNIPIEEGGEDAERVIEVEWEESAESNYSVDIEITGYDHRGLLNEVLQAVAESKTNISAVTGRTGRNKMVIIHMTILIRNIEHLQSVVEKIKRVKDIYSVQRIMQ
>NZ_CP045802.1|WP_028597534.1|4119852_4120296_-|D-tyrosyl-tRNA(Tyr)-deacylase
MKVVVQRCSSAHVAVDGETTGRIGRGLLLLVGLTHEDGEADLRWMADKIAGLRIFEDESGKMNLSVKEAGGDILSVSQFTLYGDARKGRRPNFMAAARPEQAEPLYEAFNEALRSAGLKVETGRFGAMMDVALVNDGPVTLVIDSKE
>NZ_CP045802.1|WP_153783986.1|4119562_4119739_-|hypothetical-protein
MRVGRKQLVLGAAGRRLLQAERREALLLEELEEDLEFAEDWACSAPLPERKQPEPDRP
>NZ_CP045802.1|WP_028597535.1|4117770_4119021_-|histidine--tRNA-ligase
MKFQKMPGTQDLLPGAVERWQLVEAKAREICRRFNFREIRTPIFESTDLFRRGVGETTDIVEKEMYTFEDRGGRSLTLRPEGTAGVVRAYAENKLYGEPDLTKLYYIGPMFRYERQQAGRYRQFHQFGVEALGSAEPALDAEVIALGYTFYTEVGLRGVRVEINSVGTPEVRADFRAKLLGFLEPKRQLLCKDCQSRMDRNPLRVLDCKVDQAHFEGAPSILDSLDEACADHFAKVKAGLDDMGIPYEINPRLVRGLDYYTHTAFEFKAEGIGAIDTIGGGGRYNGLVGEIGGPDQPGVGLGLGLERTVLILEHQQGEASTAQPLDVYLVALGEAAEREVSRQLHALRAAGLSADRDYQGRKMKAQMKSADRYAARFTAILGDDELAQGQIALKRMDTGEQRMVPLGELAAAIQGE
>NZ_CP045802.1|WP_043110899.1|4115898_4117731_-|aspartate--tRNA-ligase
MSSIIHCGRLSKADVGKTVELKGWVQRRRDLGGVLFIDLRDRTGIVQIVFNPDFSGDALAVADRARSEYVLAVKGKVVERDEETRNPNLETGEIEVRVTEIEVLNAAKTPPFPIEDGIEVDETLRLKYRYLDLRRPEMQRTLLLRSKAAKIFRDFLDGEQFVEVETPILTKSSPEGARDYLVPSRVHAEEFFALPQSPQLYKQLLMVGGIERYYQIARCFRDEDLRADRQPEFTQVDIETSFLSQDELLAMMESLAQRLFKETIGVDIPAPFQRITYADAIDKYGSDKPDLRFGLEIEDITDIVSTSDVKVFASVAAGGGVVRALNAKGCAGWSRKELDDLQPFAARYGGKGLAWITVKDGEWRGPIVKFLKAEEIQALTERLGVEEGDLLTFSADKKKVVADVLGNLRLKVGRQLGLIDDSAYKFAWVVDFPLLGWDEEAKRYVAEHHPFTRPKDEDLHLFETDPGAIRAQAYDLVLNGYEVGGGSMRIYKREVQEQMFQALGFSMEEAHDKFGFLLDAFEYGTPPHGGIAFGFDRLVMLLTNRSNLRETIAFPKTASATDLLMDAPAQVDLAQLQQLHIRTVPKPGSKPAAPQGGQPAEAAAGAPAQG
>NZ_CP045802.1|WP_153783985.1|4114990_4115746_-|tRNA-threonylcarbamoyladenosine-dehydratase
MLNQFSRTELAFGPEGIDVMKRSTVAVLGIGGVGSIAAEALARTGVGRIILIDKDVVDITNINRQIHALTTTVGQPKADLMRDRIQLINPECEAISLRMFYTEETYEKLFEYPLDYVLDASDTISYKVHLIKQCLERNIPIISSMGAANKMDPTKFTVTDISKTHTDPIARVVRQKLRREGVRKGVKVVFSSETPKKPREDVTQRIVPDNAPEIRKAQQPPASNAFVPPVAGLIMVSVAVRDLLEKNGVEV
>NZ_CP045802.1|WP_028597537.1|4113771_4114821_-|adenosine-deaminase
MEMSLMRRLPKIELHCHLDGSVRPATAAEIAEEEGIELSCADLRELTGRMTAPPSCSSLVEYLERFELPLLLMQTRSALRRIAYEAAEDAALDNVRYLEVRFAPQLHTRGGLSVDEIVTSVAAGLAEAEAKYGHCVRMILICMRHHGQMDNEEVVRAASRFMPLGVVGVDLAGDEAGYPNELHAEVFELAHRLGLPITIHAGEAAGACSIRCAVEKLRARRIGHGVRLREDAEVTQLIRERRIPLELCVISNVQTKAVPSMDLHPIRDYLDSGLLVTVNTDNPTVSGTNQTREYENLAHRFRFSERDIKKVARHAIEAAFVDEERKRQLKASFEREWQELGLTAAEAQA
>NZ_CP045802.1|WP_028597538.1|4112115_4113441_-|replication-associated-recombination-protein-A
MDLFDYKEEERQPRARLLADRMRPQTLDEYIGQEDVVGPGTLLRRAIEGDQVSSLLLFGPPGSGKTTLAHIISRRTEGEFVKLNAVDATVKDVRDVIERAKSSKSLYGRKTILFLDEVHRFNSSRQDALLPAVEQGIIIFIGATTENPFHSVNGALLSRSTLFRLHALESRHALEAMRRAIADKERGLGFMKLDARPEALEHIAGMAGGDIRRALNALELAAVTTPSEPDGTVVVTLEVAQESIRSRAVQADESTQYDVLSAFHKSIRGSSDAALFWFLYAVEKLGMDPMVFIRRLIVACSEDIGLANPQAMLQAVASMDAYHKIGWPEAKYNVAQAILFAVESPKSNATALAIGKAMAKMDAVGTAEVPLHLRDTHYKGSQQLGHVGYQYPHDFPGHYVDQLYYPERLAGSTVYEATRQGMEDKIRHNQQQRRSAPSQRR
>NZ_CP045802.1|WP_153783984.1|4110008_4111373_-|Mn(2+)-uptake-NRAMP-transporter-MntH
MKNERAVGNEAALESGGWRRSGGEPSLAEANRSLQVPRKGSWLRKLLAFMGPGYLVAVGYMDPGNWATDLAGGSLFGYTLLSVVLLSNLIAMVLQSLAGKLGIVTGRDLAQACRDHYSKPVALMLWALCELAIAACDLAELIGTAIALNLLFGLPLLWGVILTSLDVMLVLLLQNKGFRYMEALVIVLIGTIGGCFLLELIWAQPVVADVLKGFVPSGQIVSNPAMLYIAIGILGATVMPHNLYLHSSIVQTRRFEQTPLGKKEAIRFSTIDSTIALGLALFINAAILIVAGAVFHTSGHTDIAEIGDAYRLMAPLMGGAAASVLFGVALLAAGQNSTLTGTLAGQIVMEGFLGLRMKPWLRRLITRLIALVPAVIVTALYGERGTTELLIFSQVILSLQLSFAVFPLVKFTSDPRNMGEFANRPLLKAVAWSCAALIAVLNLYLLAMTVGGWF
>NZ_CP045802.1|WP_101807920.1|4125929_4126442_-|adenine-phosphoribosyltransferase
MNYKDYIRVIEDFPQPGIRFKDITTLLGDGKAYRAAIEDMKAALKDKQIDLIAGPEARGFVIGAPLALALGVGFVPIRKSGKLPGETVEASYDLEYGKDKLAIHKDAIAPGQRVLIADDLLATGGTIATTMDLIRQVGGEVVGASFLIELSYLNGREKLGGTDVFSLIQY
>NZ_CP045802.1|WP_153783989.1|4126462_4128886_-|single-stranded-DNA-specific-exonuclease-RecJ
MIPSKTRWRIRELDASGEEKAAKLAAQLRLSPLAARLLVLRGQESPEQAERFLHGGVEELHDPYELLGMEAAVRRIRQAADGGERVLVYGDYDADGVSSTSLMLYLLRELGMRHDYYIPHRMKEGYGLNVPAVERAAEQGFSLIITVDNGISAVEPIARARELGLSVVVTDHHEPPESLPEADAIVNPKQPGCPYPFKGLAGAGVAFKLAQALLGRPPLEWSDIAALGTVADLMPLEDENRFLVRCGLETMRRSPKPGFKALAEACGTALESVTASDIGFQMGPRINAAGRLEHADAAVRLLVSEDLAEAAGLAGELDELNVRRRAIVEQMTLEAEEAWQERCRRADEAGEPHPGVIVLAREGWNPGVIGIVASKLLDRHFRPAVLLGHDLETGLCKGSARSIPGFDLYEALSASKHLMEHYGGHAAAAGMTLKHEHLAELERGLCLEAARQLQPEDYVPVSEIDLVCLPEEASLKTIEQLALLEPFGSGNPLPKVLLQGARLAELRTIGKDQSHLKLSLGKPGASALDAIGFGLGGLSEQLAGSSAADIVGELSVNEWNGRKRPQLMIRDLAVRQPRVYDHRGTRDPLALVARLRERLLREGATGAVIASPARLQGPLRQETAAAASGAAGGFRCCDPAELPAGGFGCRELALLEPPSSWAELEAGLRLTPGLAAVHLLYPKQQPAGADWTERERMGQLYARLRRLAPLPGGRAEAARQLAQQAGCPSAAAALALAVFTELGFLREEGGALALEPAPGRRELTESASWRAAREESRLAALLQDSPEAISAWLSQLRPELQAESILN
>NZ_CP045802.1|WP_153783990.1|4128948_4129845_-|cation-diffusion-facilitator-family-transporter
MAIKLQPAADSGKRGTAVHIGLALAKGTSGALLGSSAVLSDAFRSAADACGSYLSSGEGARRGRSALSRRWLGGAEHAPAYLFSILLMLIGLELAMLAVQDLLDPPDLYPRWPAAFVVPACLVIRLLLVRGAAPATEWLSSIAATAGAGAAWAGGESGIEWLLYMDPIASALIAAVLVSKGYGLIMQAGRPRIETRQADDGLASDLMELIQRVDGVVTVEAVQPVHNGGKLAADIVISVNPRISVMEGSEIAGRVRTLVQKRFLQIVEMRICVEPYNPGYPYKSNHDPNQEHMPTLLQ
>NZ_CP045802.1|WP_084136638.1|4129861_4130785_-|protein-translocase-subunit-SecF
MRNFKESKIDFVKYSKYFYLFAIVVTLGGIISLASLGLNYGVDFSSGSSVDVQSSKSLESQRAEIETFLTEGGYGKHNAPTFGQDRMTIRFDEVLSQDQENKLKTDLKAKFDPAASVEVNTVDVEIAREMQWNALKAMIVASIGIVLYMAIRFEWRFGLAAIVSLVHDAFLVISIFSVFRLEVNLPFIVAILTIIGYSINDTIVIFDRIRENLRFAKIKSPDDLRKLVNDSIWQTMTRSINTAVTVLFAAAALFVLGSESIRLFSLAILIGLFCGAYSSIFIASPLWLLMKSKSKQKQAPAGNPAAS
>NZ_CP045802.1|WP_052332950.1|4130795_4132067_-|protein-translocase-subunit-SecD
MKRMLAFLLIVVVSLGVIGATSPALLDKTRLGLDLKGGFEILYQATPLYEGGTVTKESLNETAKSLEKRVNQTGVSEPEVTTEGADRIRIRIAGMEESKEAELRETLVKPANLTFRSARGCKDGEGYCKIELTGQDFKENGAALQQSALNEYGISIKLKDASKFAEVTREVAKLTNGKNVLAIYLDEEEISAPSVRSEINQSEASITGSFTRDEAMALRDTINLGALPLKLEVKYTQSVGATLGQKSLDDTIFAGVIGTVFIVLFMLIFYRVPGIAASVSLIIYTWLLLAAHIALDATLTLPGIAAFILGVGIAVDANIITAERIKEELRSGKSLNSAFRAGSKTSLRTIIDSHVTTIIASLVLFFIGVGSVKGFAITLLLSVLISLISNVVVSRYLLWLMIKSGRFAKPGYYGVKESEIRAL
>NZ_CP045802.1|WP_028597529.1|4132151_4132385_-|hypothetical-protein
MSEDEIAAELFVLCESKAEEFRWIGYESVTGPDIWECVHAKYAKSGAPPLYRLVNDILSLKPQQLMHHLTMSAWQNP
>NZ_CP045802.1|WP_153783991.1|4132659_4134246_+|stage-V-sporulation-protein-B
MTKQTFIKGAMILLAAGVVNRILGFVPRIALPRVIGAEGVGLYQLCYPFLGVLLTLITGGIPVAVAKWVAEAESQGGGARVRQIFRTAMGLTVALGLIMTSVMLLSAKWITTRVLTDPRVYEAFLVMAPMLLLIGVSSVYRGYFQGKQNMIPTAQSQVVETVLRIAAQLTLAALLLPMGLQWAAAGAMMGTVLGEVASLLVMLHHARKDRLEHPRERDGLDMPAEGAALPLEPLPAGRAPVLRKLLRLSVPITGSRLVGSLSYLLESILTARSLAAAGIATGAATAQYGALQGMIIPLLLLPTALTYSLSVSLVPSLSAAAARGDRAAIHKRLHQSLRLALVSGAPFVVIMGLLAEPLCRILYDHAEIAPLLTLLAPVGIFIYLQGPLQAALQALDKPGTALLNTTIGAAVKLYLIVELASRPDLGIYGAVIAISVNIVLVTLLHGISVLRISGFRMKLPDFVKVGAAMIIMGAACRWIMSHHPLSLEWLGLAAACTISALLYLALMAVMGIIDRHDLRRIPGIGRWF
>NZ_CP045802.1|WP_028597527.1|4134293_4135079_-|DUF421-domain-containing-protein
MDLGSLLLRTVLIYFVVFLIMRLMGKREIGKMSVFDLVISFMIAEIAVLVIEDTERPLLDGIVPMVILMAVQVGIAYIGMKNRRIRLLFDGKPSVIIADGKLDPEEMKKQRYNLDDLLQQLRENQIARVADVEFAILETSGKLSVIPKEQEESGAGGGKGGEADEQGGQDSAGGSGASRKADGVQHKPVQMKLPASYRFETLPIPLIMDGKVLDQSLERLEKNRFWLKQQLRKFNVSDYKQVFFCSVDHKGELFVDVRKKQ
>NZ_CP045802.1|WP_028597526.1|4135279_4135669_+|TIGR04086-family-membrane-protein
MNPIKTVPKVRLGSPMLAGLVFAALWLALGALLLSLLLYAGSLNESSLPAWSLGIHGAAALCGGFTSGKRSGSKGWYHGGLLGLGYGLLVLIISFLAADAGIGARTGILFLIVALAGAFGGMVGVNLRK
>NZ_CP045802.1|WP_101808235.1|4135805_4136609_+|inositol-phosphorylceramide-synthase
MNQVTIYTILTSALLIGFGTGRNPLRAAWVFVRNLATRPRYLLLFASLLGILFLNKFELTLEKAMKPQPDFTPYIFSFEGRFVENFQQLFHAEWLTPFLAFFYIVVFQSVLVASLGIYMFRDRSGRQFKATCYAVMINYLVAIPFYLFLPVKEVWAYDPNVHFYMLEAFPAFESMYRGLSGLDNCFPSLHTSISVTMALLAARSGNRRWAWFAGINAAIIIFTIFYMGIHWLTDMLGGLGLAVFSVALAYRLADLSSIRKPLPTVQG

Crispr_ID: NZ_CP045802_19

• CRISPR_ID: NZ_CP045802_19
• CRISPR_location: 4207380-4207928
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 10 spacers

Consensus repeat of NZ_CP045802_19

Consensus_repeat	Method
CGAGNTNCTCGGNTTTTCCGCGTAACTCC	CRT

spacers of NZ_CP045802_19

>19.1|4207409|23|NZ_CP045802|CRT
ACCATTCGGGCCCACGTTTGAAC
>19.2|4207461|23|NZ_CP045802|CRT
GCCGTTCGGGCACTCGTTTGAAC
>19.3|4207513|23|NZ_CP045802|CRT
CCCGTCCGGGCACGCGTTTGAAC
>19.4|4207565|23|NZ_CP045802|CRT
GCCGTCCGGGCCCACGTTTGAAT
>19.5|4207617|23|NZ_CP045802|CRT
CCCGTCCGGGCACGCGTTTGAAC
>19.6|4207669|23|NZ_CP045802|CRT
GCCGTCCGGGCCCACGTTTGAAT
>19.7|4207721|23|NZ_CP045802|CRT
CCCGTCCGGGCACGCGTTTGAAC
>19.8|4207773|23|NZ_CP045802|CRT
GCCGTCCGGGCCCACGTTTGAAT
>19.9|4207825|23|NZ_CP045802|CRT
CGTCGGTTCGGCACCCGCTTGCC
>19.10|4207877|23|NZ_CP045802|CRT
ACCGTCCGGGCCCGCGCTTGAAT

CRISPR arrays and Neighbor proteins around NZ_CP045802_19

CRISPR arrays

The CRISPR arrays of NZ_CP045802_19

>merge|NZ_CP045802|19|4207380-4207928|CRT
CGAGTTACTCGGGTTTTCCGCGCAACTCCACCATTCGGGCCCACGTTTGAACCAAGTTACTCGGGTTTTCCGCGTAACTCCGCCGTTCGGGCACTCGTTTGAACTGAGTTACTCGGATTTTCCGCGTAACTCCCCCGTCCGGGCACGCGTTTGAACCGAGCTGCTCGGTTTTTCCGCGTAACTCCGCCGTCCGGGCCCACGTTTGAATCGAGCTGCTCGGGTTTTCCGCGTAACTCCCCCGTCCGGGCACGCGTTTGAACCGAGCTGCTCGGTTTTTCCGCGTAACTCCGCCGTCCGGGCCCACGTTTGAATCGAGCTGCTCGGGTTTTCCGCGTAACTCCCCCGTCCGGGCACGCGTTTGAACCGAGCTGCTCGGTTTTTCCGCGTAACTCCGCCGTCCGGGCCCACGTTTGAATCGAGCCGCTCGGTTTTTCCTCGTAACTCCCGTCGGTTCGGCACCCGCTTGCCCGAGTTACTCGGTTTTTCCGCGTAACTCCACCGTCCGGGCCCGCGCTTGAATCGAGCTGCTCGGTTTTTCCGCGTAACTCC

>NZ_CP045802|19|5|4207380-4207928|CRT
CGAGTTACTCGGGTTTTCCGCGCAACTCC	ACCATTCGGGCCCACGTTTGAAC
CAAGTTACTCGGGTTTTCCGCGTAACTCC	GCCGTTCGGGCACTCGTTTGAAC
TGAGTTACTCGGATTTTCCGCGTAACTCC	CCCGTCCGGGCACGCGTTTGAAC
CGAGCTGCTCGGTTTTTCCGCGTAACTCC	GCCGTCCGGGCCCACGTTTGAAT
CGAGCTGCTCGGGTTTTCCGCGTAACTCC	CCCGTCCGGGCACGCGTTTGAAC
CGAGCTGCTCGGTTTTTCCGCGTAACTCC	GCCGTCCGGGCCCACGTTTGAAT
CGAGCTGCTCGGGTTTTCCGCGTAACTCC	CCCGTCCGGGCACGCGTTTGAAC
CGAGCTGCTCGGTTTTTCCGCGTAACTCC	GCCGTCCGGGCCCACGTTTGAAT
CGAGCCGCTCGGTTTTTCCTCGTAACTCC	CGTCGGTTCGGCACCCGCTTGCC
CGAGTTACTCGGTTTTTCCGCGTAACTCC	ACCGTCCGGGCCCGCGCTTGAAT
CGAGCTGCTCGGTTTTTCCGCGTAACTCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_153784010.1|4214263_4215595_+|spore-germination-protein	unknown	unknown	gnl|CDD|377020
NZ_CP045802.1|WP_153784001.1|4198649_4199951_-|trigger-factor	unknown	unknown	gnl|CDD|234956
NZ_CP045802.1|WP_153784012.1|4216705_4217848_+|Ger(x)C-family-spore-germination-protein	unknown	unknown	gnl|CDD|274338
NZ_CP045802.1|WP_153784009.1|4213369_4214113_-|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|379312
NZ_CP045802.1|WP_153784003.1|4204160_4204502_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153784002.1|4200050_4200956_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153784005.1|4205006_4206851_+|asparagine-synthase-(glutamine-hydrolyzing)	unknown	unknown	gnl|CDD|273676
NZ_CP045802.1|WP_153784006.1|4208159_4208813_-|RdgB/HAM1-family-non-canonical-purine-NTP-pyrophosphatase	unknown	unknown	gnl|CDD|184835
NZ_CP045802.1|WP_028599066.1|4208809_4209556_-|ribonuclease-PH	unknown	unknown	gnl|CDD|178914
NZ_CP045802.1|WP_153784000.1|4197821_4198418_-|ATP-dependent-Clp-endopeptidase-proteolytic-subunit-ClpP	unknown	unknown	gnl|CDD|178955
NZ_CP045802.1|WP_153784764.1|4201392_4201821_+|EamA-family-transporter	unknown	unknown	gnl|CDD|225308
NZ_CP045802.1|WP_101807938.1|4196543_4197797_-|ATP-dependent-protease-ATP-binding-subunit-ClpX	unknown	unknown	gnl|CDD|235422
NZ_CP045802.1|WP_153784008.1|4211767_4212124_-|cupin-domain-containing-protein	unknown	unknown	gnl|CDD|380393
NZ_CP045802.1|WP_153784007.1|4210979_4211534_+|phosphatidylglycerophosphatase-A	unknown	unknown	gnl|CDD|224186
NZ_CP045802.1|WP_084136632.1|4203141_4204062_+|YihY/virulence-factor-BrkB-family-protein	unknown	unknown	gnl|CDD|377085
NZ_CP045802.1|WP_101807941.1|4209755_4210841_-|hypothetical-protein	unknown	unknown	gnl|CDD|227688
NZ_CP045802.1|WP_153784765.1|4212221_4213256_-|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|293811
NZ_CP045802.1|WP_153784004.1|4204498_4204846_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153784011.1|4215591_4216719_+|GerAB/ArcD/ProY-family-transporter	unknown	unknown	unknown
NZ_CP045802.1|WP_028597477.1|4201983_4202940_-|sugar-binding-transcriptional-regulator	unknown	unknown	gnl|CDD|225263

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_153784010.1|4214263_4215595_+|spore-germination-protein	gnl|CDD|377020	pfam03323, GerA, Bacillus/Clostridium GerA spore germination protein.	7.6525e-123
NZ_CP045802.1|WP_153784001.1|4198649_4199951_-|trigger-factor	gnl|CDD|234956	PRK01490, tig, trigger factor; Provisional.	1.93227e-165
NZ_CP045802.1|WP_153784012.1|4216705_4217848_+|Ger(x)C-family-spore-germination-protein	gnl|CDD|274338	TIGR02887, Spore_germination_protein_B3, germination protein, Ger(x)C family. Members of this protein family are restricted to endospore-forming members of the Firmicutes lineage of bacteria, including the genera Bacillus, Clostridium, Thermoanaerobacter, Carboxydothermus, etc. Members are nearly all predicted lipoproteins and belong to probable transport operons, some of which have been characterized as crucial to germination in response to alanine. Members typically have been gene symbols gerKC, gerAC, gerYC, etc. [Transport and binding proteins, Amino acids, peptides and amines, Cellular processes, Sporulation and germination].	4.87151e-49
NZ_CP045802.1|WP_153784009.1|4213369_4214113_-|methyltransferase-domain-containing-protein	gnl|CDD|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	1.52168e-24
NZ_CP045802.1|WP_153784007.1|4210979_4211534_+|phosphatidylglycerophosphatase-A	gnl|CDD|224186	COG1267, PgpA, Phosphatidylglycerophosphatase A and related proteins [Lipid metabolism].	8.65062e-47
NZ_CP045802.1|WP_101807941.1|4209755_4210841_-|hypothetical-protein	gnl|CDD|227688	COG5401, COG5401, Spore germination protein [General function prediction only].	1.06958e-16
NZ_CP045802.1|WP_153784006.1|4208159_4208813_-|RdgB/HAM1-family-non-canonical-purine-NTP-pyrophosphatase	gnl|CDD|184835	PRK14822, PRK14822, XTP/dITP diphosphatase.	3.95616e-90
NZ_CP045802.1|WP_028599066.1|4208809_4209556_-|ribonuclease-PH	gnl|CDD|178914	PRK00173, rph, ribonuclease PH; Reviewed.	1.12962e-163
NZ_CP045802.1|WP_153784000.1|4197821_4198418_-|ATP-dependent-Clp-endopeptidase-proteolytic-subunit-ClpP	gnl|CDD|178955	PRK00277, clpP, ATP-dependent Clp protease proteolytic subunit; Reviewed.	3.53849e-149
NZ_CP045802.1|WP_153784764.1|4201392_4201821_+|EamA-family-transporter	gnl|CDD|225308	COG2510, COG2510, Predicted membrane protein [Function unknown].	5.7382e-36
NZ_CP045802.1|WP_101807938.1|4196543_4197797_-|ATP-dependent-protease-ATP-binding-subunit-ClpX	gnl|CDD|235422	PRK05342, clpX, ATP-dependent Clp protease ATP-binding subunit ClpX.	0
NZ_CP045802.1|WP_153784008.1|4211767_4212124_-|cupin-domain-containing-protein	gnl|CDD|380393	cd06988, cupin_DddK, Dimethylsulfoniopropionate lyase DddK and related proteins, cupin domain. This family includes mostly bacterial proteins homologous to dimethylsulfoniopropionate lyase DddK from marine bacterium Pelagibacter. DddK cleaves dimethylsulfoniopropionate (DMSP), the organic osmolyte and antioxidant produced in marine environments, and yields acrylate and the climate-active gas dimethyl sulfide (DMS). DddK contains a double-stranded beta-helical motif which utilizes various divalent metal ions as cofactors for catalytic activity; however, nickel, an abundant metal ion in marine environments, confers the highest DMSP lyase activity. Also included in this family is Plu4264, a Photorhabdus luminescens manganese-containing cupin shown to have similar metal binding site to TM1287 decarboxylase, but two very different substrate binding pockets. The Plu4264 binding pocket shows a cavity and substrate entry point more than twice as large as and more hydrophobic than TM1287, suggesting that Plu4264 accepts a substrate that is significantly larger than that of TM1287, a putative oxalate decarboxylase. Thus, the function of Plu4264 could be similar to that of TM1287 but with a larger, less charged substrate. Proteins in this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold.	0.000750891
NZ_CP045802.1|WP_084136632.1|4203141_4204062_+|YihY/virulence-factor-BrkB-family-protein	gnl|CDD|377085	pfam03631, Virul_fac_BrkB, Virulence factor BrkB. This family acts as a virulence factor. In Bordetella pertussis, BrkB is essential for resistance to complement-dependent killing by serum. This family was originally predicted to be ribonuclease BN, but this prediction has since been shown to be incorrect.	6.30674e-69
NZ_CP045802.1|WP_153784765.1|4212221_4213256_-|MBL-fold-metallo-hydrolase	gnl|CDD|293811	cd07725, TTHA1429-like_MBL-fold, uncharacterized Thermus thermophilus TTHA1429 and related proteins; MBL-fold metallo hydrolase domain. Includes the MBL-fold metallo hydrolase domain of uncharacterized Thermus thermophilus TTHA1429 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.	3.68258e-48
NZ_CP045802.1|WP_153784005.1|4205006_4206851_+|asparagine-synthase-(glutamine-hydrolyzing)	gnl|CDD|273676	TIGR01536, Asparagine_synthetase_1, asparagine synthase (glutamine-hydrolyzing). This model describes the glutamine-hydrolysing asparagine synthase. A poorly conserved C-terminal extension was removed from the model. Bacterial members of the family tend to have a long, poorly conserved insert lacking from archaeal and eukaryotic sequences. Multiple isozymes have been demonstrated, such as in Bacillus subtilis. Long-branch members of the phylogenetic tree (which typically were also second or third candidate members from their genomes) were removed from the seed alignment and score below trusted cutoff. [Amino acid biosynthesis, Aspartate family].	1.28137e-156
NZ_CP045802.1|WP_028597477.1|4201983_4202940_-|sugar-binding-transcriptional-regulator	gnl|CDD|225263	COG2390, DeoR, Transcriptional regulator, contains sigma factor-related N-terminal domain [Transcription].	3.45386e-108

Protein sequences

>NZ_CP045802.1|WP_153784005.1|4205006_4206851_+|asparagine-synthase-(glutamine-hydrolyzing)
MCGFTGWIDWTRDLTLHSEDLERMTATLALRGPDASGTWISGSCALGHRRLSVMDPENGAQPMIRSQDGQKFVIVYNGELYNAPELKRELEGRGRRFTTTCDTEVLLTAYMEWGPAAVEKFNGIFAFAIWDDQEQKLFLARDRVGVKPLFVSHAGGQFVFGSEPKALLAHPAVSSDVGAQGIAELFIVGPARTPGVGVYKDLTELLPGKCMTVDRGGARVHTYWELRSREHEHGVEETAAHVGELLRDTVERQLASDVPVGTLLSGGLDSSALTALAVDFYGRSGAGSLDTFSVDYVDNDKFFKSHAFQPNADAPWIEKMVSHLGTAHHDIKFDTPELVAALDDALTARDLPGMADVDASLLLFCREIKKGVTVAISGEAADEVFGGYPWFHREESLNAGTFPWALASPMRAELLSPEMQEWTRPLEYIGDRYSEAVAAVPHLSGENELQRKMRTMSYLNITRFMPTLLDRKDRMSMAAGLEVRVPFCDHRLIEYVFNIPWAIKTAGDREKGILRQSLRGALPDDVLFRKKSPYPKTHNPNYLNAVRSKLMEVLDDPSSPILPLINAKKVREIAESDAASSNIPWFGQLMSGPQLFAYLYQVNRWLTQYGVRVV
>NZ_CP045802.1|WP_153784004.1|4204498_4204846_-|hypothetical-protein
MADYGTEGQRKHYYVAVGAGQVLEDKEAAAYELEIVATEEEKDGLKALFAEMSSMDEAAMVHFHSHPFGSASVEEMNQGYEGILKQIYTLVYRLGTEETRRHVASLNLDIGGLPG
>NZ_CP045802.1|WP_153784003.1|4204160_4204502_-|hypothetical-protein
MNVLEAHVARSLEKDGTPCAEVQVRTDDPQCEQVLAYFSLSEDQDYDLVSIVRDDADLLTDWFDNSMHTAYEDITMQWFENESLKTDWGRRETFKQQVLASGQVREDLRELLG
>NZ_CP045802.1|WP_084136632.1|4203141_4204062_+|YihY/virulence-factor-BrkB-family-protein
MTRAVELGKNLYARFQDDEVPALGAQLTYYLLLSFFPFLIFLVSLLGFLNLNGDELIADMIAMMPAEGGETVRTILGEVSTGGSGALLSVGMIGTIWAASNGVNAIIKGLNKAYDEEEDRPFWKVRGLSLLATIVLAAVVILVVVLLVFGRGVGEFLFQWLDYPAGFEALWTIVRYVLPIAAMALVFTLLYWFTPNRRLTFREALPGACFASLGWVVTSIAFSYYVSQFGNYTKTYGSLGGVIVLLIWLYLSSIIIVLGGEINAALSFGSAGVEKKRPAKSFGLRLFRKKGVPSGRAPGPDKRIPL
>NZ_CP045802.1|WP_028597477.1|4201983_4202940_-|sugar-binding-transcriptional-regulator
MSEKLEKIVEAARLYYQMDFSQQDIAKKLGVSRPTVSRFLQQAKADGIVQITIHDPLENNDLVCRQLEKRFGLNRAIVVSTPSHEDAVVKKYIGEAAAAHLYETVAEGDTIAVTWGSTLYEVAQRLPLKSVRDVKVVQLNGGLSYSETNTFASEIVHLFAGAFNTSPHLLPLPAIVDQPLVKRAIEADRHIAKILEMGRQANIAVFTVGVPTADSLLVRANYLSAEELDIVHQAGKGDICSRFIDIDGNICLSELDDRTIGIRLEELRRKEHSVLVAGGIDKADAVFAAVKGGYPNTIVTDAFTARHLLERDQARVTA
>NZ_CP045802.1|WP_153784764.1|4201392_4201821_+|EamA-family-transporter
MMLWLPYALLSAVFAALVSIFGKIGLKDLDANSATALRAVIMALFLLGVVAVQGKFGQVGEIFAQRKALAFVAMSGAAGALSWLFYFLALKAGTVSQVGPVDKLSVVFAIVLALLFLGEKITVWNGVGVLMITAGVILTSLK
>NZ_CP045802.1|WP_153784002.1|4200050_4200956_-|hypothetical-protein
MDDSTRGEKDNLYLFPSSLDHYQEQLTRLLESEHYAEAKRLLQFLLQCRGEEPRHYEEWSNLLAWLEMAFPGGAEEEDGEPSEDDLRRTALSPAEQDESYVQQVLYIMKNHPMLDQQLLALERAAHLRSSEVDETIRRWLEQETLHPMVQFKALQCLRRRGDAGVVRLERLGETAELEIERTPLDLDDYPEPVRLILERVEGVTETMDPTLPHFARELWKECLQYLYGSSAYARMLSEEEAVVDSYAAALHLTLLLAVYGTAEEEKIRHTYGITDELRFRYEQACRAMRQITDLQEGSGDG
>NZ_CP045802.1|WP_153784001.1|4198649_4199951_-|trigger-factor
MTATWEKIETNVVAIDVEVGAEQVKEALDQAFKKVVGRVNVPGFRKGKVPRSIFESRFGVESLYQDAIDILLPTAYSEALKDTGIEPVDRPEIDVEQFGKGQPFKFKAKVTVKPEVKLGEYKGIEVPAASSDVTDEELSAELERLQQRHAELVVVEEGAAENGDTVVIDFEGFVDGEAFEGGQAERYSLELGSNSFIPGFEEQVVGLATGDFKDVEVTFPEEYHAENLAGKAAVFKVKLHEIKRKNLPALDDEFAKDVSEFDTLDEFKQDLSKKLQERKEKENEQARETALVDKIAAAAEVEIPEAMINTEVDYLLRDFENRIKQQGLNMELYYQFSGQDEAALRGQMRSDAEKRVLNNLVLDAIAKQESIEISEEEVGEELENLSKMYSRPAAELRDIFERNGNLDNMKEDLKLRKTIKFLLDNSKIASEVA
>NZ_CP045802.1|WP_153784000.1|4197821_4198418_-|ATP-dependent-Clp-endopeptidase-proteolytic-subunit-ClpP
MNLVPIVVEQTNRGERSYDIYSRLLKDRIIFLGSAIDDDVANSIIAQLLFLAADDPEKDIHLYINSPGGSVTAGMGIYDTMQFIKPDVSTICVGMAASMGSLLLTAGAKGKRFALPNSEVMIHQPLGGVRGQASDIKIHADWIIKTKQKLNQIYVDRTGQPYEKIERDTDRDNFLSADDALAYGLIDKVIAVPEAGLL
>NZ_CP045802.1|WP_101807938.1|4196543_4197797_-|ATP-dependent-protease-ATP-binding-subunit-ClpX
MFKFNEEKGQLKCSFCGKSQDQVRKLVAGPGVYICDECIELCTEIVEEELGHEEELDLKDIPKPKDIRAILDSYVIGQEAAKKSLSVAVYNHYKRINSQSKLEDVELQKSNIMLVGPTGSGKTLLAQTMAKILNVPFAIADATSLTEAGYVGEDVENILLKLIQAADYDVEKAERGIIYIDEIDKVARKSENPSITRDVSGEGVQQALLKILEGTVASVPPQGGRKHPHQEFIQIDTTNILFICGGAFDGLEQIIKRRIGKKVIGFNTGDGTKDMKAGEYLSLVLPEDLLKFGLIPEFVGRLPVISTLEPLDEAALVRILAEPKNALVKQYQKLLEMDNVKLEFEAGALDAIAKEAIKRNTGARGLRAIIEGIMLEIMYEAPSREELSTCVITEKVVQDRVVPELTAKKGKKKEESA
>NZ_CP045802.1|WP_153784006.1|4208159_4208813_-|RdgB/HAM1-family-non-canonical-purine-NTP-pyrophosphatase
MSGGYIVVATGNAGKVKEFAHAFAGLGLSVRSLKDYPELPEPVEDGDTFAANARIKAGTIGRLLGAPVLADDSGLCVDALDGAPGVYSARYSGPGATDARNNAKLLRELEAAGADASGRAAAPPDGGRLLSAGRFVCALALYVPERDGYIESEGAMEGFVLDAPRGSGGFGYDPLLWLPELGRSAAELSVEEKQRVSHRGEALRRLLAELERSGIRL
>NZ_CP045802.1|WP_028599066.1|4208809_4209556_-|ribonuclease-PH
MRSDGRKPSQLRPVAIAVGVNKYAEGSVLIEAGDTKVLCTASVEERVPPFMKGQGKGWVTAEYSMLPRATHTRSQRESQRGKVNGRTMEIQRLIGRALRSVVNLQALGERTITLDCDVLQADGGTRTTSITGSFVALALAVAKIDARSPFAVYPLTDYLASTSVGIIGGEPRLDLHYEEDSRAKVDMNLVMTGAGSFVELQGTGEEEPFSREELDRLLSLGEQGIRELIEIQQMALGAAGARIGTGRA
>NZ_CP045802.1|WP_101807941.1|4209755_4210841_-|hypothetical-protein
MEQQRYRWIRKAALTGALTLPVMVAGCGWFSPSDSKAVDPPQGETGSAITGADGQTSAAATGSAEVSAQGEASGLTVYLKDAEGYLAPVTIQAKLDSKLTAEAQALELLVDGGAYSKLLPEGFSGVLPQGTQVLNVQVNEKTKLATVEFSKQFSDYNEQDERTMLEAITYTLTGLDGIQGVELWEEGERLQEMPVGQYPLDRALTRAIGINLEADSGVDYSLSTPVTLYFSSKTELGDPYFVPVTRLVPRTTDKLTAALDQLAEGPLEESRLLPVWLQDVSVDKITQNKDTITLDLKDEAYKKGDVAPAEMMRAVVLSLTDNAGVDQVQIKLNGASDFKDELDTSYTEPVSRPEQLNAFKS
>NZ_CP045802.1|WP_153784007.1|4210979_4211534_+|phosphatidylglycerophosphatase-A
MSKPAAYALNSKAVAEATAEWLAKRGVTKAEIAELTFFLQKDYYPDLSLAECEENIEAVLSKREVQNAILTGIQLDLLAEEGRLLPPLQEMIRNDEGLYGCDEILALSIVNVYGSIGLTNFGYVDKLKPGILVRLNDKNDGQIHTFLDDIVGAIAAAAASRIAHRKQAEREEARGERQDDVPLP
>NZ_CP045802.1|WP_153784008.1|4211767_4212124_-|cupin-domain-containing-protein
MKIYQLPGREWPIDAFSSQGVMFSGITRHDGRIQLSSMRIEANGIVGRHVAEASQLFLLIDGEGWVSGADGKRISVKAGQAAYWEAGEEHESGSRTGMTVIVVEGGQLVVEMEELASF
>NZ_CP045802.1|WP_153784765.1|4212221_4213256_-|MBL-fold-metallo-hydrolase
MGAGRDPLQAEPLGGGWLRVPVPLPYSLRFVNAYLVPEPDGGWTVIDPGLNTEDARTTWRELQQQAGIARGDIRRVLLTHQHPDHYGLSGWMQQEHGCPVWMTRQAHRYAVRMWGTDSRFPRELEAWFRCHGMPDELLALLGPHLDSFRERVEPQPQPSYLEPGEIVELGGRSWRLIDAPGHAPGAVCLYEPGRRELIAGDQVLARITPNISLLPGDGVDPDPLRSYLASLAELAELPTERVYPGHREPFADAGKRAREIAEHHARRLEHLLGLLAERGEASAFELCELEFGVHLRRNIHNLRFALSETLAHLAYLERDGRAEARFRADGAIRYRGVTRENGIG
>NZ_CP045802.1|WP_153784009.1|4213369_4214113_-|methyltransferase-domain-containing-protein
MSEWFVRSFGEDYKIAYRHRDWEQAEREVGRLAARLELRPGARIADIGCGMGRHSLALSRLGYEVSGLDLSQALLREARSQPGSEAVSWFEGDMRRMPFEDGQFDAAVNLFTSFGYFEEDREHLQVLREMRRILRPGGRFVIDFLNAEQVKSTLVPESRRVDEETGTVIVERRCIEHGRVVKKIELTDAAGGEPRRYTESVRLLGEPWFRSALAEAGLVLESAGGGYDGEPYEPERSKRLVLFGRRP
>NZ_CP045802.1|WP_153784010.1|4214263_4215595_+|spore-germination-protein
MLQAIRERFASATDVKTHRITNSRFIAEVAFIATLVDESKVSDMVLVPFAKEEVPFDELLRRNPNFQPLDDPARWTDSLLRGFVLVKLNSAIYKMDAARIIRNSTPETTVESTIEGPQIALSEDLMDSINMIRSRYASPDLLEEEFTVGSLSKTRVVMLYDQVRVDPAVLEIVRLKLRSIQTDVLSASGQLAKFMNDNRKRLFPVEMVTERIDRLSVGLSKGKIIVMMQGSMFALLLPIVFTDLMSATEDRYESFWTSLLLLSLRFIALLMTTTLPALYIAAISYNPELFRVQLAFSIAGSRASVPYPSFIEVFIMLFMIEMLVEASVRLPKYIGSTATTVGGLILGQAAQQAGLVSSIMIIVTSVMAISNFVIPVYSLSLSVRFIKYPLIALAIFFGLPGVAGGVFAGLIYLCSQRSFGKPYFRLRLPIDWRHADIGEVKAE
>NZ_CP045802.1|WP_153784011.1|4215591_4216719_+|GerAB/ArcD/ProY-family-transporter
MNRYFYYSFIMVAMLNLMLYVPSVLLEERMTGAVSSLLVAIGLGTLTAYAVTSAMARYPGLGVPEILRLYLPEWIVKTLLSLFAFVFFFASSFALVGYTLLLNRVLTPDLPAWNLLLVLGLICIYGSTRSSMTLLFLLEMTMVLTIPVILFILFKGIRSPDVAWNAIYTIAQYVTVRPTLTSVAAGTFIFTGYINLAIFNRLNPPNFRLKGRWLIPLLGSGILLTTFFLPIGYHGTMAVDRYMYVWTQTADSMTMSFGFIERVLFLFLLVYLALTLLYTSIGWHQAIEFIHSLRKDRKFEVDSTETPASSWWISSIFFALSVASMFFLDEKLTLAVAEIWLTFRMFIEQGAAALLFLLSFKRPPDAAKEAAHDSA
>NZ_CP045802.1|WP_153784012.1|4216705_4217848_+|Ger(x)C-family-spore-germination-protein
MIRLDAPRRPSLPLRAFSRRLAALLLAAALLLQATGCGFIDIDKRFFVVALSVDKSGNDKKPYRITIRLSIPNSKTEPGMEKSQIETIDAKEISEGLRILKSRVDKEIDLGHCKVLLLGEQLARDDISDAVEWMMRRRDIQSSAFVAVGQPDGRRILEQMPLSERYSGNTLFLTFGGDATKSSFIRPIKLFDLFRRINEHGMDPYLPIVSLTKNGYEVDRLALLDKTRIRAVLGPDETQLFNQLDQQYINSTIKTSFEDRTVMLAVMDLTVREKIRRAGAGQGTLDLSIHAGGTLEEGPNDILHRHAAVVEASFERDLAAKTEALLRKIQRSGVDPLQFGLRFRATHRSKQAFEEWQEMYPTLKFRVRTDVDIQGAGRIK

Crispr_ID: NZ_CP045802_20

• CRISPR_ID: NZ_CP045802_20
• CRISPR_location: 4843841-4843951
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_20

Consensus_repeat	Method
GCGGTTGAGCGAAGCCGAGCATGCGGA	CRISPRCasFinder

spacers of NZ_CP045802_20

>20.1|4843868|57|NZ_CP045802|CRISPRCasFinder
ACGAGCGGCGGATGCGCGGTTGAGCGAAGCCGAGCCGTCGGAGCTCGTGGCAGACGG

CRISPR arrays and Neighbor proteins around NZ_CP045802_20

CRISPR arrays

The CRISPR arrays of NZ_CP045802_20

>merge|NZ_CP045802|20|4843841-4843951|CRISPRCasFinder
GCGGTTGAGCGAAGCCGAGCATGCGGAACGAGCGGCGGATGCGCGGTTGAGCGAAGCCGAGCCGTCGGAGCTCGTGGCAGACGGGCGGTTGAGCGATGCCGAGCATGCGGA

>NZ_CP045802|20|16|4843841-4843951|CRISPRCasFinder
GCGGTTGAGCGAAGCCGAGCATGCGGA	ACGAGCGGCGGATGCGCGGTTGAGCGAAGCCGAGCCGTCGGAGCTCGTGGCAGACGG
GCGGTTGAGCGATGCCGAGCATGCGGA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_028598816.1|4845411_4846281_-|aminoglycoside-6-adenylyltransferase	unknown	unknown	gnl|CDD|377357
NZ_CP045802.1|WP_028598823.1|4837708_4838833_-|hypothetical-protein	unknown	unknown	gnl|CDD|185594
NZ_CP045802.1|WP_153784791.1|4848845_4849772_-|peptidase	unknown	unknown	gnl|CDD|223862
NZ_CP045802.1|WP_153784227.1|4846294_4846714_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028598811.1|4850157_4851264_-|dipeptide-epimerase	unknown	unknown	gnl|CDD|239435
NZ_CP045802.1|WP_153784224.1|4842548_4842863_-|hypothetical-protein	unknown	unknown	gnl|CDD|227178
NZ_CP045802.1|WP_153784222.1|4830420_4837458_-|carbohydrate-binding-protein	unknown	unknown	gnl|CDD|224389
NZ_CP045802.1|WP_153784788.1|4828550_4829039_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|378968
NZ_CP045802.1|WP_153784228.1|4846855_4847665_-|inositol-monophosphatase	unknown	unknown	gnl|CDD|223559
NZ_CP045802.1|WP_153784789.1|4839339_4839900_-|DUF1273-family-protein	unknown	unknown	gnl|CDD|237461
NZ_CP045802.1|WP_153784220.1|4827157_4828444_+|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_CP045802.1|WP_028598810.1|4852309_4853926_-|peptide-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|173869
NZ_CP045802.1|WP_153784230.1|4851314_4852313_-|LD-carboxypeptidase	unknown	unknown	gnl|CDD|132882
NZ_CP045802.1|WP_153784229.1|4847661_4848747_-|phosphotransferase	unknown	unknown	gnl|CDD|366736
NZ_CP045802.1|WP_153784790.1|4840056_4841361_-|DNA-recombination-protein-RmuC	unknown	unknown	gnl|CDD|376878
NZ_CP045802.1|WP_153784221.1|4829125_4830262_+|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|369777
NZ_CP045802.1|WP_153784231.1|4853965_4855180_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|223521
NZ_CP045802.1|WP_153784225.1|4843153_4843702_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|213752
NZ_CP045802.1|WP_153784223.1|4841427_4842552_-|SH3-domain-containing-protein	unknown	unknown	gnl|CDD|119407
NZ_CP045802.1|WP_153784232.1|4855182_4856103_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|224094

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_028598816.1|4845411_4846281_-|aminoglycoside-6-adenylyltransferase	gnl|CDD|377357	pfam04439, Adenyl_transf, Streptomycin adenylyltransferase. Also known as Aminoglycoside 6- adenylyltransferase (EC:2.7.7.-), this protein confers resistance to aminoglycoside antibiotics.	1.05256e-155
NZ_CP045802.1|WP_028598823.1|4837708_4838833_-|hypothetical-protein	gnl|CDD|185594	PTZ00395, PTZ00395, Sec24-related protein; Provisional.	3.47673e-13
NZ_CP045802.1|WP_153784791.1|4848845_4849772_-|peptidase	gnl|CDD|223862	COG0791, Spr, Cell wall-associated hydrolases (invasion-associated proteins) [Cell envelope biogenesis, outer membrane].	4.66829e-27
NZ_CP045802.1|WP_153784231.1|4853965_4855180_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	2.54505e-178
NZ_CP045802.1|WP_028598811.1|4850157_4851264_-|dipeptide-epimerase	gnl|CDD|239435	cd03319, L-Ala-DL-Glu_epimerase, L-Ala-D/L-Glu epimerase catalyzes the epimerization of L-Ala-D/L-Glu and other dipeptides. The genomic context and the substrate specificity of characterized members of this family from E.coli and B.subtilis indicates a possible role in the metabolism of the murein peptide of peptidoglycan, of which L-Ala-D-Glu is a component. L-Ala-D/L-Glu epimerase is a member of the enolase-superfamily, which is characterized by the presence of an enolate anion intermediate which is generated by abstraction of the alpha-proton of the carboxylate substrate by an active site residue and is stabilized by coordination to the essential Mg2+ ion.	1.85579e-135
NZ_CP045802.1|WP_153784224.1|4842548_4842863_-|hypothetical-protein	gnl|CDD|227178	COG4841, COG4841, Uncharacterized protein conserved in bacteria [Function unknown].	6.45736e-26
NZ_CP045802.1|WP_153784222.1|4830420_4837458_-|carbohydrate-binding-protein	gnl|CDD|224389	COG1472, BglX, Beta-glucosidase-related glycosidases [Carbohydrate transport and metabolism].	1.30949e-84
NZ_CP045802.1|WP_153784788.1|4828550_4829039_+|helix-turn-helix-domain-containing-protein	gnl|CDD|378968	pfam12840, HTH_20, Helix-turn-helix domain. This domain represents a DNA-binding Helix-turn-helix domain found in transcriptional regulatory proteins.	4.66389e-06
NZ_CP045802.1|WP_153784228.1|4846855_4847665_-|inositol-monophosphatase	gnl|CDD|223559	COG0483, SuhB, Archaeal fructose-1,6-bisphosphatase and related enzymes of inositol monophosphatase family [Carbohydrate transport and metabolism].	1.47245e-57
NZ_CP045802.1|WP_153784789.1|4839339_4839900_-|DUF1273-family-protein	gnl|CDD|237461	PRK13660, PRK13660, hypothetical protein; Provisional.	2.33731e-74
NZ_CP045802.1|WP_153784220.1|4827157_4828444_+|MFS-transporter	gnl|CDD|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like 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.	4.65176e-58
NZ_CP045802.1|WP_028598810.1|4852309_4853926_-|peptide-ABC-transporter-substrate-binding-protein	gnl|CDD|173869	cd08504, PBP2_OppA, The substrate-binding component of an ABC-type oligopetide import system contains the type 2 periplasmic binding fold. This family represents the periplasmic substrate-binding component of an ATP-binding cassette (ABC)-type oligopeptide transport system comprised of 5 subunits. The transport system OppABCDEF contains two homologous integral membrane proteins OppB and OppF that form the translocation pore; two homologous nucleotide-binding domains OppD and OppF that drive the transport process through binding and hydrolysis of ATP; and the substrate-binding protein or receptor OppA that determines the substrate specificity of the transport system. The dipeptide (DppA) and oligopeptide (OppA) binding proteins differ in several ways. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	0
NZ_CP045802.1|WP_153784230.1|4851314_4852313_-|LD-carboxypeptidase	gnl|CDD|132882	cd07025, Peptidase_S66, LD-Carboxypeptidase, a serine protease, includes microcin C7 self immunity protein. LD-carboxypeptidase (Muramoyltetrapeptide carboxypeptidase; EC 3.4.17.13; Merops family S66; initially described as Carboxypeptidase II) family also includes the microcin c7 self-immunity protein (MccF) as well as uncharacterized proteins including hypothetical proteins. LD-carboxypeptidase hydrolyzes the amide bond that links the dibasic amino acids to C-terminal D-amino acids. The physiological substrates of LD-carboxypeptidase are tetrapeptide fragments (such as UDP-MurNAc-tetrapeptides) that are produced when bacterial cell walls are degraded; they contain an L-configured residue (L-lysine or meso-diaminopimelic acid residue) as the penultimate residue and D-alanine as the ultimate residue. A possible role of LD-carboxypeptidase is in peptidoglycan recycling whereby the resulting tripeptide (precursor for murein synthesis) can be reconverted into peptidoglycan by attachment of preformed D-Ala-D-Ala dipeptides. Some enzymes possessing LD-carboxypeptidase activity also act as LD-transpeptidase by replacing the terminal D-Ala with another D-amino acid. MccF contributes to self-immunity towards microcin C7 (MccC7), a ribosomally encoded peptide antibiotic that contains a phosphoramidate linkage to adenosine monophosphate at its C-terminus. Its possible biological role is to defend producer cells against exogenous microcin from re-entering after having been exported. It is suggested that MccF is involved in microcin degradation or sequestration in the periplasm.	1.22709e-114
NZ_CP045802.1|WP_153784229.1|4847661_4848747_-|phosphotransferase	gnl|CDD|366736	pfam01636, APH, Phosphotransferase enzyme family. This family consists of bacterial antibiotic resistance proteins, which confer resistance to various aminoglycosides they include: aminoglycoside 3'-phosphotransferase or kanamycin kinase / neomycin-kanamycin phosphotransferase and streptomycin 3''-kinase or streptomycin 3''-phosphotransferase. The aminoglycoside phosphotransferases inactivate aminoglycoside antibiotics via phosphorylation. This family also includes homoserine kinase. This family is related to fructosamine kinase pfam03881.	3.17576e-14
NZ_CP045802.1|WP_153784790.1|4840056_4841361_-|DNA-recombination-protein-RmuC	gnl|CDD|376878	pfam02646, RmuC, RmuC family. This family contains several bacterial RmuC DNA recombination proteins. The function of the RMUC protein is unknown but it is suspected that it is either a structural protein that protects DNA against nuclease action, or is itself involved in DNA cleavage at the regions of DNA secondary structures.	2.37473e-89
NZ_CP045802.1|WP_153784221.1|4829125_4830262_+|methyltransferase-domain-containing-protein	gnl|CDD|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	8.28424e-07
NZ_CP045802.1|WP_153784225.1|4843153_4843702_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|213752	TIGR02954, RNA_polymerase_ECF-type_sigma_factor, RNA polymerase sigma-70 factor, TIGR02954 family. This group of sigma factors are members of the sigma-70 family (TIGR02937). They and appear by homology, tree building, bidirectional best hits and one-to-a-genome distribution, to represent a conserved family. This family is found in certain Bacillus and Clostridium species.	3.25579e-41
NZ_CP045802.1|WP_153784223.1|4841427_4842552_-|SH3-domain-containing-protein	gnl|CDD|119407	cd02696, MurNAc-LAA, N-acetylmuramoyl-L-alanine amidase or MurNAc-LAA (also known as peptidoglycan aminohydrolase, NAMLA amidase, NAMLAA, Amidase 3, and peptidoglycan amidase; EC 3.5.1.28) is an autolysin that hydrolyzes the amide bond between N-acetylmuramoyl and L-amino acids in certain cell wall glycopeptides. These proteins are Zn-dependent peptidases with highly conserved residues involved in cation co-ordination. MurNAc-LAA in this family is one of several peptidoglycan hydrolases (PGHs) found in bacterial and bacteriophage or prophage genomes that are involved in the degradation of the peptidoglycan. In Escherichia coli, there are five MurNAc-LAAs present: AmiA, AmiB, AmiC and AmiD that are periplasmic, and AmpD that is cytoplasmic. Three of these (AmiA, AmiB and AmiC) belong to this family, the other two (AmiD and AmpD) do not. E. coli AmiA, AmiB and AmiC play an important role in cleaving the septum to release daughter cells after cell division. In general, bacterial MurNAc-LAAs are members of the bacterial autolytic system and carry a signal peptide in their N-termini that allows their transport across the cytoplasmic membrane. However, the bacteriophage MurNAc-LAAs are endolysins since these phage-encoded enzymes break down bacterial peptidoglycan at the terminal stage of the phage reproduction cycle. As opposed to autolysins, almost all endolysins have no signal peptides and their translocation through the cytoplasmic membrane is thought to proceed with the help of phage-encoded holin proteins. The amidase catalytic module is fused to another functional module (cell wall binding module or CWBM) either at the N- or C-terminus, which is responsible for high affinity binding of the protein to the cell wall.	2.08456e-60
NZ_CP045802.1|WP_153784232.1|4855182_4856103_-|ABC-transporter-permease-subunit	gnl|CDD|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	2.1795e-107

Protein sequences

>NZ_CP045802.1|WP_153784225.1|4843153_4843702_+|sigma-70-family-RNA-polymerase-sigma-factor
MLARRAAAGDEEAFLELMDAERHRLRRIASACLSGEHDVLEAVQETACRAWLKRRELRQPDYMGTWLVRILLRVCADELKRSRRQPPSAEAAELLERRGREAAPLADEAGEADLRLDLAAVVDALEPPYRDVVRMKYHRDMTLTEIARALEKPPGTVKTWLHKALGQMRGQLRKGEEGKHGG
>NZ_CP045802.1|WP_153784224.1|4842548_4842863_-|hypothetical-protein
MKLVVEPEAARWYKRELGLEDGEQLRVFVRLGGCGSVQPGLSLGIMKDESRSPGLRKEQEGLVFFMEEDQLWYLDAKELHLVYDEAEREAVIEVRDGPLKGGAE
>NZ_CP045802.1|WP_153784223.1|4841427_4842552_-|SH3-domain-containing-protein
MICRLTMLLIALLLALPAWTAGEATAAGASYKVGTKSLAVREDADSGSAVKGYLKQGTVVQVTEEKYGWAKLSGGGLKGWAAAHFLVASSGSASASGSGSSVTTASAAKDSGWKSVAGSGVRLRSGPGTGYDVVGSVTTGDRVKILKQEGSWTRVTTESGQTAWMSSQYIGGSVAVSSGGGLGPATGSSRGSLQGKLIAVDPGHGGNDPGMIGTTHGTEEKDLTLSTSKLLAEELRSLGARVVMTRTKDGEKPALPERVKTAADAEADAFVSVHYNSAKNQASGTLVFYYSKSKDAPLAHAVEGRLQGLSLRSNGIAFGDYHVLRENRLPSVLVELGFLSNAKDEKEARTASYQKAAAKAIAEGLQDYFARKSS
>NZ_CP045802.1|WP_153784790.1|4840056_4841361_-|DNA-recombination-protein-RmuC
MGLQLLVLAGVGLLLLRRPGSGRGGQDALIRELRAELERLRAELRRESSEQAAQARQEASASARQSREELAAALNATNRMLMANMNDMAQQQKHLLDHFSERLSELTRVSETKLELVRGTVEEKLRLLQEDNGRRLEQMRATVDEKLHATLEQRLGESFKLVSDRLELVHQGLGEMKNLASGVGDLRKVLTNVKTRGTLGEIQLGNLLEQTLTVEQYERNAATRRGSSERVEFAVRIPDKHNPKQWLYLPIDSKFPIEDYQRLLDALDADDHAAAAECSRLLDARIKAEAKSIQAKYLDPPNTTDFGIMFLPVEGLFAEVLRRPGLWEYVQREHRVVIAGPTTLTALLNSLQMGFQTLAIQQRSSEVWQVLGAVKTEFGKFGDLLDKTQKKLQEASNSIDAASVRSRAIERKLRKVQELPAGETPDLLLEAAGD
>NZ_CP045802.1|WP_153784789.1|4839339_4839900_-|DUF1273-family-protein
MVNLLATGYRAHELNIFNQKHEAIPYIKAAATSRLVPLLEDGLEWLLSPGGYGFDLWAVEAALELKRDYPQLKVSILTAYANVDEKWKDDRKLYYEELLRQVDHHASVSKQSYEGVWQLTARDSLLVRKSDAMLLFYDEEMGEGSPRYFKERALKRQETGDDYPLLTISAETVQSIADDARSAAFE
>NZ_CP045802.1|WP_028598823.1|4837708_4838833_-|hypothetical-protein
MQSDIETDGQPADGWHHSTSMERSLLGRLVNRRNKVKAEKPPKYIPKQLVGAEALSPVSLQLSFSKPLAPEELEAAPAYLKLSGGLQVTGCPRLKNGSRASYIVPTSLQQPGKRYACAFRGGDKLGFRAGVDRIFFRRAVACAYDTVELAASLGDAVVDVGRVTEAVRPEFAGSGFELSADNVFEGRYYQIVPPLDGLTVQISPERGQTLEATYIPGTQLASARQAPRFRLPAGFAFTSGQRYAVSAEWARIGQDEFTAPAYRLPAPPHSASPHSAPPHSASPHSASPHSASPHSASPHSAPPHSAPPHSASPHSASPHSASPHSASPHSASPHSAPPHSAPMLPSPKLPAPAPERLRPLAALPAPSPARRSSN
>NZ_CP045802.1|WP_153784222.1|4830420_4837458_-|carbohydrate-binding-protein
MKPSIPSAQQRGSGGGRARPPEARKGKAKRWLSALTAAALAAGMLPAATSAAPEAGTLPAYYNPALTPEKRTEDLLARMTVEEKVGQMVQAERASVTPEDVRTYHLGSVLSGGGSFPNGKQADSTLENWTELYESYQNGALSTRLGIPLLYGVDAVHGHNNVKGATLFPHNIGLAAAGSEELAERVGEAAAAEIRATGINWTFAPALAVVQDIRWGRTYEGFGDSPELAAKLGAAYIRGLQGEKPEQLADREHVVATAKHFVGEGYTAGGVNQGNVTAYSEEDIWKLEKPVYEAAVKAGVGTVMASYHSIQGLKMHANERLLQDKLKGELGFKGFVISDYNAIDQITRDSAGNAVSGLKAQVRTAVNAGVDMIMEPDKWKQVYADLKALAEEGAVPMSRIDDAVTRILTVKFRSGVFEQPYGDRDMQQAFGSQASRAVAREAVSRSLVLLKNDPVRGADGVEAPILSLLPTMKNLLVAGKNANDIGRQSGGWSITWQGSAGAITPGTTILEGLQAAAKAAGATVTFNEHGRGAAGKDAAIVVLGEKPYAEGSGDASSLDLDTEDQATLDNIRAANPDLPVVLVLVSGRPMTVAKQLDQVQGLVAAWLPGTEGAGVADVLLGEREFEGKLPIRWPFELSAYAKPDPGAEEFLFQTGYGLQKNQATPPLPEAPQPETPENPGYVQIEAESFVAQSGIQTEKTQDAGGGDNIGYIDDGDWTEHEVELEGGLYDVEVRYASWGDSSGLRIVDGNKQASATIPLPRIASYQDWGSAKAKDIELPGGPCKQKLRLSFLGGSFNLNWVKLTRTGDAPSPTTVVCTEEPGGPGTPIEPEIVQEDAVQSWISRERDPGDIRWYYAPRWQEGDSKLAPQAPLDVVKPNEAAGEVIELDADTAYQSIFGIGSSMEESTVGNLMKMSPEKRHELLVQLFDKEKGAGMSLVRVTIGTADFTGQPFYSYNDLPPGETDPELKKFSIQKDRDLGIISTLQEIQAINPDVKFFGSPWSAPGWMKTTGSMIKGEVLEPYLPVYADYLVKFVQAYGDEGIPIEMLTMQNEPLLEIEYPSTKMSWQQQGRLAALLRAKLDAAGLGEVKILTFDHNPGDTMAYPAQLLRDPAAYAAVDGTAFHDYGGELSEMTRLKELFPEKNVYLTERAVWGTQGADRIAQYFRNWARSYNSWVVMLDSDIRAHQWTGVPDPTPVIQDSADRDHYWLAPETYLMAQFSKFVLPGYERIDSNYGSKDTVTNVAFRSPDGKKIVAVLINQTASDQPVKLLSDGTQISAVVPAKSVATYSWTRPELGRTAPGRFAASSFDRAEGSYSADAATGVVDGLNADPAQGQAAFDYGVNVRKAGRYTLDLSYAGQPADASVTVKAGGATAAYVPVTRDTYGEFAAVRVQLDLPAGEQQLRLEAAGTGYRLRELRLQPAAGEAALPQRVEAEAASSTAHALLLEAPAGASKDAVSLHGGSELNVRVSAPESGLYQLQYRYRTESEADATVSWSVYGGSPIHSDALPASSAWTTASGTIRLSQGAQQLRLTAADGPLALDWVQLGPVLQVKDNPRLIAVPGTASADDYAAMSGFKPGAGGSADGRQLGESDAGDWADYRLAVPEAGRYTVTLELQSQNGGIGAFSLKLGESVLATYGVPQIYNNWITVRKTIDLPGGEQTLRLAANVGGFNVGSLAVEPLRPQMAGADGALQLEAESYFDADRNAIETNRSSGTANVGYTNAGNKLHYGVDVPQAGRYKVTYRYATQQSGVSAALLADGQSVGAVSLPSTGGWGTYREVSGIVALPAGPQQLSVLIQGDGFNLDWLRLAPTDEEPAVQPERAAIAKASLKAGKHAKPQAVTLASGTADAAVYYTLDGSLPSAESGRRADGPIQVEGTVVIRAVAVKAGMDASFVSAFTYVTGPADPQPSTDPGTSPQPSESPGSSPTPSAGPTATPEPTGGPIATPAPSASPSASPTASPGGSLTSGQPKLDAASGIASVAVSQAELDQAGSAGGKITINVPFVAGATGYTVILPAEALRSGASSMELRLPNGTLLLPAGWLQGAALAGADVRLTLADAADRSALTAGQQAASAGLPVYRISLDSGGKPVVPAASHPAASVSVPAKLAGQALADSHRIAVRLLDGSRSLPVPSGRYVAGAGAGSGSVKFDVRASGTYAAVLSGAEFRDLTRHAWAQQAIEALAARGIVQGVDEQRFQPGAEVRRADLLLLLVRAFEFSADGEASFRDIPAGAYYEEAARIAKLLGLAQGREDGRFDPLAPVSRQELMTLLARAAELAGEPLEPAALSSLAAFRDSGSVAPYAAASAAALVQAGIVGGDNGALKPQGTASRAETAAMLYRLLERS
>NZ_CP045802.1|WP_153784221.1|4829125_4830262_+|methyltransferase-domain-containing-protein
MRIDLGCGAAKHPGCIGIDTRGLPDVDLVHDFDTPLPLSDDSVDFAMLADSAQFSADPLRLMKELYRVCRHGAVVCIAAPYAHASSHLANPAYRSLLSEQSPRYWTSHPVCYVDPDEYRFCAERSWSLQGEEAPDLRLVRLEFFYYPQYEGMYEPHELSLLRQSQMNVAHHFMMHLIVVKQSVSEDEMQWLSVQPMEEPSYVQELRFPVRSGSEEPFLYPGPMELMMSAAAPSAKESGQADVPAAEKSSEADGSAESSGEEAAGAHPQRSDAAADGPDEAPGAGAELGSGGTDDAEAELGSGETDSAGAGLGSGEAADRAGNLPDRVVEPARRGAPPARASRPRVKPGGGKRTRRSAAAKPAPKKRTRTRNRASSKRT
>NZ_CP045802.1|WP_153784788.1|4828550_4829039_+|helix-turn-helix-domain-containing-protein
MKILDQFYKATEPSTIKEIADQLGEVPAKVYYHARKLESIGLLELKETRLINGITAKYYKAFEGSVQVRRDDVDESIRTVFASEAQKLVARMFDASKQKYLDNQSSGKKRIGTVLNSDLYLNKEESEAFVEMIQDFIREHSKPASPGQEAHHFFFSFSHIEE
>NZ_CP045802.1|WP_153784220.1|4827157_4828444_+|MFS-transporter
MSLPAAGLAPAPSRPFRALLAHRSFMLLLAARMTSRFGDSIDSIAYSWMVYQLTGSKLMMGSLFALNFVPGILFSLFIGVLIDRIPQKTILVASYAARGLSVAATAALLGLGLLEPWHLFVFTFLNSTLECFATPTETSLVPRLLPKPLLLSGNSLSASLSRSAELAGLAAAGAIIAWTGLAGAILVDASTFLLSALLLLFLAVPARPDEDRPSPSQDDAGAKKTAYWQDFKLGLSFVRSHSLLILTLMTGALLNVGLIPHNVMGPVYVKDVLHAGPSVLSLLGVCLLTGMILSGLAIGAWGSRFRKSSLIVFGCFLLGASQGLYFLPAAIEWQPAVIVAALAFSSGAAIPFINTPLSTYMMEVTPAGMLGRVSSLSSMISSALLPVGAIAVGAVGSLVPVETLYLGAGLLMVLPAFFLLTRKSFMKI
>NZ_CP045802.1|WP_028598816.1|4845411_4846281_-|aminoglycoside-6-adenylyltransferase
MRSETDMMELFLATAREDERIRAVTLEGSRTDPNAAPDLFQDYDISYLVSDMDSFQADPDWIDRFGSRLWLQTPEAMELFPAELGRRFSYLILFEDGNKLDLTLIPMEEASAYAAEDKLLKVLLDKDGLLPEVPPSTDEDYRVSAPSEAYFHDCRNEFWMVSTYVAKGLWRREILYAMDHLNGILRPMLLQMLEWQAGYRTGFSVSVGKNRKRIRRWLEEDEWEGLMQTFPGGSEEEVWEALFAAVRLFRRSGEQVAARLGCRYPAEEDERMAAYLRRVQSLPADAGRF
>NZ_CP045802.1|WP_153784227.1|4846294_4846714_-|hypothetical-protein
MGEEALNGMRLYVVDRVEKGSSCRCAVLQLSCGACSGWSEAEVARCGQPFDLVRWACCLQPLRRMTPEQAMRAVQERGSGWGEPRRRLVLGALLELRERLTRPERPKERPVWTGEGRLGAAERDERAMLERAASYYEIL
>NZ_CP045802.1|WP_153784228.1|4846855_4847665_-|inositol-monophosphatase
MTEHQAVLARAREVAELAAREAAALARDYFTRDKQVQDKGDSGDLVTVADTLAEEIILAHIRAAFPDHEIRSEETGWHGAPGDWLWLVDPLDGTNNYAIGLPVYGVSITLLYRREPLLGVICDSHLDRLYVAEQGKGAFVDGAPLSIRRCPSVPRMTVGWIQGHAVGKDERVLALKARLEGSFKRVLRLWAPALQWCMLARGDLDAMVLYNSEGDDLYAGLLLAREAGAAVVDFDGEPFEGMNAEPYLIAAHPDHLPELIALVRDGLKV
>NZ_CP045802.1|WP_153784229.1|4847661_4848747_-|phosphotransferase
MEGYASTDGCREGAAMTTKIIFSSPRVGETSDEQLQRMLDRHGLGRLLAWSRTGQGAMSQTLRIETSTGAFILKGNPLYPGHLEEERWFTEQLASRTRLPLPIPYIVDERTDLFGWSYAIMPCLPGRHLGDLADEGGFAGAEAAAEALHEIHRWKEPVYGEYDPISRRIVPFEGGYYGWLFERILYWLHDAARFSAIGAEDTAWTEERLRQAQPDFAELGQAALCMGDFKPGNFLLSSRPADASRLAVSGLFDLTNAYFGDPLADLAKLLVYYRGRGRQDLAACFLRAYAEGMEDERGLGSRLGVHLLHQNVLDWGCLKAMGAADWPAELTFRAWAAAQQADLADWLAAIEPRSAGRRETP
>NZ_CP045802.1|WP_153784791.1|4848845_4849772_-|peptidase
MDFEQRLDLCEGNRLQTQLLLGERVLVAEEKDGWARIHAPSQATAKEPDGYPGWMPLAQLVFDGAAGEPERGGPAPIAVVTAESAWLHLGSAPLGAAADIAPSAPAASGGAGAAASEAAEPEAACEPQPWIELSFLTELPVLSERGDWAEVALPQGGGGWLRRSDIRLREPRETSALVGEGRHAGRVIVEQAKRYLGLPYLWGGISSFGYDCSGLAYAMHRAAGFVIPRDASDQALGGLPVEREELTPGDLLFFAYEEGKGRIHHVGIYAGGGRMIHSPRTGRCVELVKLDESYELYREHCASRRYWK
>NZ_CP045802.1|WP_028598811.1|4850157_4851264_-|dipeptide-epimerase
MNIESIKAMRQSTPMARPFRTALRTVREAESIIVRVRDQDGRIGWGEAPSTVVITGDSLESIQAAIEHTLAPPLIGQSLLGYERLLQTVHGAMVGSPSAKAALDMAIYDLVAQHCGLPLYQFLGGYKDRLETDFTVSVGEPEEMARDAEASVRGGFDVLKIKVGKDAAELDVRRIEEIRARVGPDVRIRLDANQGWSVKEAVRAIRRMEDLGLNLELVEQPVRAHDVEGLKAVTDAVQTPIMADESVFSPAEALRVLQLRAADLINIKLMKAGGIYKAQQINALAEQYGVECMVGSMIESRVAVTAAAHLAASKKNITRFDFDAPLLIGSDIVDGGVRYDGRVMTFPDAPGLGIRGVRIRPGAGAAVS
>NZ_CP045802.1|WP_153784230.1|4851314_4852313_-|LD-carboxypeptidase
MMLRPPALKPGDTVGIPALASPGDPAQIEAASRQLERLGLRVRLGRTVSLRRGYLAGSDEERADELMEMFADPSISGIVCARGGYGTARIADRLDYGVIRAHPKAFWGYSDITFLHAAIGRLAGLVTFHGPMMIDLQEQPAGSGGFDHARPHPVTLEAYRQLLAPRRPQLGEEHGPLRPIVPGEASGPVVGGNLTLIVSTLGTRYELDTRGRLLLLEDIDEEPYRVDRMLMQLRQAGKLDDAAGIVVGDFHNCGPAKRKASLSLDEVLQEHLGAAGKPALAGFRIGHGSPQLAVPLGVEARLSTAERRLDFAESGWAEDEAASGSAADSERG
>NZ_CP045802.1|WP_028598810.1|4852309_4853926_-|peptide-ABC-transporter-substrate-binding-protein
MKKLSMLLMSVMLAGGVLAACGNDSSNGEAGEGEAAGKILRYNNGKEPTSLDPPIGFDQISYDIVNNAFEGLARLGKDDKPEPAMAAEWKVSDDGLVYTFTLRDGVKWSNGDPVKASDFEFAWKRLLNPETASDAAFLAYPIVGAEDYNSGKGSADAVGIKAKDDKTLEVTLRHPAAWLVQMTASPAFFPVHQATVEGNAQWAGEASTIVSNGPFTITEWKHEEELKMVKNKDYWDAGTVKLGGVTYKMVNDTNTAYQLFTTGELDTTGSIPADMADQLFADGKVKVEESAGTAFYRFNTTMEPFTNKSIRQAFVAAVDRQQLVDLVLRQKHKPAVGFVSPGLEDAAGGDFRDVGGDLIGFDAAKAKELLAAGMKEAGYSALPPITLTYSTNDVNQKVAQALQAMFKDNLGVEVKLESKESKVMTAEQKALQLQLSRSSFLPDFADPINFLDGFQSDNPFSRTGWKNDKFDELIQGAYEQADEKQRYEMMHEAEKILMDDAPILPLYYYNSVNLESDKLSGVVRHAFGFIDFKWAELK
>NZ_CP045802.1|WP_153784231.1|4853965_4855180_-|ATP-binding-cassette-domain-containing-protein
MWRRSDRDHRKKAALSAVAAPPAPEAAQARPERADSGGAPEPDLGRAAQAARPLGEVILEVDDLRVSFRTHGGQVQAVRGVSLSLRQGETLAIVGESGCGKSVTARSLMRLLPEHAAVLGAGSSIRWKGRELTKLKEKELRKLRGAEIAMIFQDAMTALNPTLTIGEQLIEGIALHRKVPRSEARRLAVDMLELVGIPSPEARLKQYLGEFSGGMRQRIMIAIAASCSPSLLIADEPTTALDVTIQAQILDLFRMLQERTGAAIVLITHDLGVVAETADRVCVMYAGEIVESGTVRELFRRPQHPYTQGLLAALPRLDRERGRSLVPIPGTPPDLFAPPPGCAFAARCPHAMEVCRLHRPQMAELDGTHAVACWLQDPRAARPPAAGAGAGSGMAGEPARTALG
>NZ_CP045802.1|WP_153784232.1|4855182_4856103_-|ABC-transporter-permease-subunit
MSVPDSLFVPMNRDAVDAEAIVRPRLSFAQEAWRRLKQNRLAFAGALLIVLLALLATVGPYLPVQSYDKQVLTDINLAPSAQHWFGTDELGRDVFARIVYGARISLFIGLAATLIDVVIGIVYGGIAGYVGGRADNVMMRFVDMLYGVPYLLIVILLMVVMSPGLATIIVALSATGWIGMARVVRGQVLSLKSSEYVLAARSMGSSGWRIIRKHLVPNAMGVILVQISFSVPSAIFAEAFLSFLGLGIQPPLASWGVMASDGLSVILSGQWWRLFFPALFISVTMLAFNLLGDGLQDIFNPRQRRS

Crispr_ID: NZ_CP045802_21

• CRISPR_ID: NZ_CP045802_21
• CRISPR_location: 4960354-4960462
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP045802_21

Consensus_repeat	Method
AGACGGCCGCAGGACAGGGCAGAC	CRISPRCasFinder

spacers of NZ_CP045802_21

>21.1|4960378|20|NZ_CP045802|CRISPRCasFinder
CAGACGGCCAGGGCAGACCA
>21.2|4960422|17|NZ_CP045802|CRISPRCasFinder
GGCCCGCAGGACAGGGC

CRISPR arrays and Neighbor proteins around NZ_CP045802_21

CRISPR arrays

The CRISPR arrays of NZ_CP045802_21

>merge|NZ_CP045802|21|4960354-4960462|CRISPRCasFinder
AGACGGCCGCAGGACAGGGCAGACCAGACGGCCAGGGCAGACCAGACGGCCCGCAGGACAGGGCAGACGGCCCGCAGGACAGGGCAGACGGCCGCAGGACAGGGCAGAC

>NZ_CP045802|21|17|4960354-4960462|CRISPRCasFinder
AGACGGCCGCAGGACAGGGCAGAC	CAGACGGCCAGGGCAGACCA
GACGGCCCGCAGGACAGGGCAGAC	GGCCCGCAGGACAGGGC
AGACGGCCGCAGGACAGGGCAGAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_153784291.1|4970278_4972528_-|phosphoribosylformylglycinamidine-synthase-subunit-PurL	unknown	unknown	gnl|CDD|234921
NZ_CP045802.1|WP_028598696.1|4950658_4951801_+|hypothetical-protein	unknown	unknown	gnl|CDD|274338
NZ_CP045802.1|WP_028598694.1|4952844_4953189_+|hypothetical-protein	unknown	unknown	gnl|CDD|334619
NZ_CP045802.1|WP_153784282.1|4948969_4950646_+|spore-germination-protein	unknown	unknown	gnl|CDD|377020
NZ_CP045802.1|WP_153784796.1|4961407_4962352_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|224096
NZ_CP045802.1|WP_153784288.1|4963811_4965092_-|phosphoribosylamine--glycine-ligase	unknown	unknown	gnl|CDD|234856
NZ_CP045802.1|WP_084137132.1|4953538_4954987_-|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_CP045802.1|WP_101808211.1|4965313_4966861_-|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase	unknown	unknown	gnl|CDD|234854
NZ_CP045802.1|WP_153784289.1|4966897_4967593_-|phosphoribosylglycinamide-formyltransferase	unknown	unknown	gnl|CDD|235544
NZ_CP045802.1|WP_153784283.1|4951840_4952662_-|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|366166
NZ_CP045802.1|WP_028598682.1|4972505_4973201_-|phosphoribosylformylglycinamidine-synthase-subunit-PurQ	unknown	unknown	gnl|CDD|235140
NZ_CP045802.1|WP_153784797.1|4968665_4970132_-|amidophosphoribosyltransferase	unknown	unknown	gnl|CDD|235984
NZ_CP045802.1|WP_052333168.1|4957415_4958417_-|polysaccharide-deacetylase-family-protein	unknown	unknown	gnl|CDD|213022
NZ_CP045802.1|WP_028598681.1|4973205_4973448_-|phosphoribosylformylglycinamidine-synthase-subunit-PurS	unknown	unknown	gnl|CDD|376904
NZ_CP045802.1|WP_153784286.1|4958782_4960189_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270451
NZ_CP045802.1|WP_084137135.1|4947782_4948973_+|GerAB/ArcD/ProY-family-transporter	unknown	unknown	gnl|CDD|281794
NZ_CP045802.1|WP_153784287.1|4960517_4961411_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223472
NZ_CP045802.1|WP_153784285.1|4955821_4957324_-|hypothetical-protein	unknown	unknown	gnl|CDD|379232
NZ_CP045802.1|WP_153784284.1|4954944_4955790_-|response-regulator	unknown	unknown	gnl|CDD|223816
NZ_CP045802.1|WP_153784290.1|4967592_4968636_-|phosphoribosylformylglycinamidine-cyclo-ligase	unknown	unknown	gnl|CDD|235439

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_153784291.1|4970278_4972528_-|phosphoribosylformylglycinamidine-synthase-subunit-PurL	gnl|CDD|234921	PRK01213, PRK01213, phosphoribosylformylglycinamidine synthase subunit PurL.	0
NZ_CP045802.1|WP_028598696.1|4950658_4951801_+|hypothetical-protein	gnl|CDD|274338	TIGR02887, Spore_germination_protein_B3, germination protein, Ger(x)C family. Members of this protein family are restricted to endospore-forming members of the Firmicutes lineage of bacteria, including the genera Bacillus, Clostridium, Thermoanaerobacter, Carboxydothermus, etc. Members are nearly all predicted lipoproteins and belong to probable transport operons, some of which have been characterized as crucial to germination in response to alanine. Members typically have been gene symbols gerKC, gerAC, gerYC, etc. [Transport and binding proteins, Amino acids, peptides and amines, Cellular processes, Sporulation and germination].	2.42681e-37
NZ_CP045802.1|WP_028598694.1|4952844_4953189_+|hypothetical-protein	gnl|CDD|334619	pfam01638, HxlR, HxlR-like helix-turn-helix. HxlR, a member of this family, is a DNA-binding protein that acts as a positive regulator of the formaldehyde-inducible hxlAB operon in Bacillus subtilis.	2.87562e-35
NZ_CP045802.1|WP_153784282.1|4948969_4950646_+|spore-germination-protein	gnl|CDD|377020	pfam03323, GerA, Bacillus/Clostridium GerA spore germination protein.	4.34171e-161
NZ_CP045802.1|WP_153784796.1|4961407_4962352_-|ABC-transporter-permease-subunit	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	2.19919e-86
NZ_CP045802.1|WP_153784288.1|4963811_4965092_-|phosphoribosylamine--glycine-ligase	gnl|CDD|234856	PRK00885, PRK00885, phosphoribosylamine--glycine ligase; Provisional.	0
NZ_CP045802.1|WP_084137132.1|4953538_4954987_-|HAMP-domain-containing-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	3.91704e-66
NZ_CP045802.1|WP_101808211.1|4965313_4966861_-|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase	gnl|CDD|234854	PRK00881, purH, bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase; Provisional.	0
NZ_CP045802.1|WP_153784289.1|4966897_4967593_-|phosphoribosylglycinamide-formyltransferase	gnl|CDD|235544	PRK05647, purN, phosphoribosylglycinamide formyltransferase; Reviewed.	6.74637e-103
NZ_CP045802.1|WP_153784283.1|4951840_4952662_-|alpha/beta-fold-hydrolase	gnl|CDD|366166	pfam00561, Abhydrolase_1, alpha/beta hydrolase fold. This catalytic domain is found in a very wide range of enzymes.	8.88186e-16
NZ_CP045802.1|WP_028598682.1|4972505_4973201_-|phosphoribosylformylglycinamidine-synthase-subunit-PurQ	gnl|CDD|235140	PRK03619, PRK03619, phosphoribosylformylglycinamidine synthase subunit PurQ.	4.21235e-159
NZ_CP045802.1|WP_153784797.1|4968665_4970132_-|amidophosphoribosyltransferase	gnl|CDD|235984	PRK07272, PRK07272, amidophosphoribosyltransferase; Provisional.	0
NZ_CP045802.1|WP_052333168.1|4957415_4958417_-|polysaccharide-deacetylase-family-protein	gnl|CDD|213022	cd10917, CE4_NodB_like_6s_7s, Catalytic NodB homology domain of rhizobial NodB-like proteins. This family belongs to the large and functionally diverse carbohydrate esterase 4 (CE4) superfamily, whose members show strong sequence similarity with some variability due to their distinct carbohydrate substrates. It includes many rhizobial NodB chitooligosaccharide N-deacetylase (EC 3.5.1.-)-like proteins, mainly from bacteria and eukaryotes, such as chitin deacetylases (EC 3.5.1.41), bacterial peptidoglycan N-acetylglucosamine deacetylases (EC 3.5.1.-), and acetylxylan esterases (EC 3.1.1.72), which catalyze the N- or O-deacetylation of substrates such as acetylated chitin, peptidoglycan, and acetylated xylan. All members of this family contain a catalytic NodB homology domain with the same overall topology and a deformed (beta/alpha)8 barrel fold with 6- or 7 strands. Their catalytic activity is dependent on the presence of a divalent cation, preferably cobalt or zinc, and they employ a conserved His-His-Asp zinc-binding triad closely associated with the conserved catalytic base (aspartic acid) and acid (histidine) to carry out acid/base catalysis. Several family members show diversity both in metal ion specificities and in the residues that coordinate the metal.	8.96852e-78
NZ_CP045802.1|WP_028598681.1|4973205_4973448_-|phosphoribosylformylglycinamidine-synthase-subunit-PurS	gnl|CDD|376904	pfam02700, PurS, Phosphoribosylformylglycinamidine (FGAM) synthase. This family forms a component of the de novo purine biosynthesis pathway.	1.82686e-40
NZ_CP045802.1|WP_153784286.1|4958782_4960189_-|extracellular-solute-binding-protein	gnl|CDD|270451	cd14748, PBP2_UgpB, The periplasmic-binding component of ABC transport system specific for sn-glycerol-3-phosphate; possesses type 2 periplasmic binding fold. This group includes the periplasmic component of an ABC transport system specific for sn-glycerol-3-phosphate (G3P) and closely related proteins from archaea and bacteria. Under phophate starvation conditions, Escherichia coli can utilize G3P as phosphate source when exclusively imported by an ATP-binding cassette (ABC) transporter composed of the periplasmic binding protein, UgpB, the transmembrane subunits, UgpA and UgpE, and a homodimer of the nucleotide binding subunit, UgpC. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.7347e-127
NZ_CP045802.1|WP_084137135.1|4947782_4948973_+|GerAB/ArcD/ProY-family-transporter	gnl|CDD|281794	pfam03845, Spore_permease, Spore germination protein.	4.40632e-19
NZ_CP045802.1|WP_153784287.1|4960517_4961411_-|ABC-transporter-permease-subunit	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	2.27663e-72
NZ_CP045802.1|WP_153784285.1|4955821_4957324_-|hypothetical-protein	gnl|CDD|379232	pfam13517, VCBS, Repeat domain in Vibrio, Colwellia, Bradyrhizobium and Shewanella. This domain of about 100 residues is found in multiple (up to 35) copies in long proteins from several species of Vibrio, Colwellia, Bradyrhizobium, and Shewanella (hence the name VCBS) and in smaller copy numbers in proteins from several other bacteria. The large protein size and repeat copy numbers, species distribution, and suggested activities of several member proteins suggests a role for this domain in adhesion (TIGR).	0.000180494
NZ_CP045802.1|WP_153784284.1|4954944_4955790_-|response-regulator	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	7.30601e-74
NZ_CP045802.1|WP_153784290.1|4967592_4968636_-|phosphoribosylformylglycinamidine-cyclo-ligase	gnl|CDD|235439	PRK05385, PRK05385, phosphoribosylaminoimidazole synthetase; Provisional.	0

Protein sequences

>NZ_CP045802.1|WP_153784286.1|4958782_4960189_-|extracellular-solute-binding-protein
MVIRNWKWALPAAAAMLILPLSACAGNPDTNNGGAASSEPSTTASPSSSPAGGEASKAPVKVVWWHSMSGELGKAADALVSGFNSTHPDVQVEAVFQGTYDESLNKMKASMDSKSGPSLIQVYEIGSRFMIDSGAVTPVQQFIDAEGYDVGSLEPNIRGYYTFGGKQYSMPFNTSNPILYYNKDLFKAAGLDPEKPPATYQEVADAAKALTKDGVTGASFAIYGWFMEQLLAAQGKELVNNGNGRDSAATESLVNQEAAVQTLEWWKGLVDAKTALNLGRKTDDTKKAFLAGQVAMTLDSTAGLRGIVDGAAGKFEVGTAFLPRPSADAEGGVVVGGASLWVLNNKPAEEQQAAWEFIKYLAEPATQAQWHINTGYFPITTKAYDEQVVKDNLVKYPQFQTAVDQLHASKPSTASQGAVMGVFPEARQLVEAAIEEAFTGKKDVKAALDDAAKQITDKIAVYNKTVSK
>NZ_CP045802.1|WP_052333168.1|4957415_4958417_-|polysaccharide-deacetylase-family-protein
MRKPAGAAVRRRAPQAAALAALTALALAAGGCGSADHVEAGGFQPSASASPGASSPSASPDAGATQPGAGAPTAIPATASPSPHPSASSGPKSPHPSPTASPHPSPSERPHTVTGDTYEKPPLQAQAGPLAEPNDGRAHTAKLEKGAKAVALTFDDGPDAATTVKILDILRKEKVKATFFVVGTQVKKYPEVMQRIVDEGHALGNHTTHHPDLSKTGKTKILQEIKDNDTLIQKAVGITPTMFRPPYGATSAELKAILSEGGRTEVLWNVDTRDWAGTSVKTMRANVAKHAKPGSIILMHSFGSKLHTAELLPLIIHDLKTAGYRFVTPDQLG
>NZ_CP045802.1|WP_153784285.1|4955821_4957324_-|hypothetical-protein
MSNSCNRINRTSRPPRSGARKPLRLLALLGACALALSGCRYTAAPADLLGPPMEAPQAGGASSSLKQLLPAGGSLSLPTRERQPEAIRSIDLDGDGSPEAVLTYSDAYGSSRILIARQEAGEWKTWAVLRSAMGTSLEWLSFVDMNGDKQPEIIAGWLVRQPGNSLTWQQYEVQVYSASDPLFEESEEGRLLKPVAELGYEAGDTGDVDGDGRQELVLVRRPGSPNEPMLEVYRFANGRLDRAATLPLEADATLYERLAIGRIAKDRFGVIAEAGAGAHSSLTLMAGWYDDGLEQVYPPVEEPDLGFNMSPVLNTDINGDGILEWSRQVEAPGQPEGTPYSDLITYTEWTQWSGLRPQDPGFVRKDMFLPVTLEYNDFSSGVSVQIPSRWRGQFTLSRPVEEPEAIIQLDYYNAKSGAIAPLWTLYGIPIKEWGSWSAAMEGKGRKPANLRTAGGYVYAAIEEPKPKAEDGWSDTDLNRYDAMRLTGEQLASSVRLQPAD
>NZ_CP045802.1|WP_153784284.1|4954944_4955790_-|response-regulator
MKILLVEDEEAIRGFVRINLKRADMEPVEAGSAEQALRLVAEQGPPDIALLDIMLPGLSGLELCSALREAYPEMGIIMLTAKSQEQDKIEALELGADDYIQKPFSPGELMARIRSLQRRMNIGAWRGPAPAAVAAPEAEGEAAAARTAAMPAPAEAEAHGAPAPSAAAPAPASVPASAAVRSGEPFRLAPGDRRLWKHDREIVLTPTEWSLVKLLLERRGQSVSRDEILSEVWGRYYVGDLKVVDVNIRRIRQKVEDDPSEPAIIETVWGFGYRWNRSDPG
>NZ_CP045802.1|WP_084137132.1|4953538_4954987_-|HAMP-domain-containing-histidine-kinase
MGVRLPVEQERSGMRSLRTKMVFSYLLLVFLTVVVLGGMFLTLIWNYYYGSASSAMKQRVATSMSLHARAMQWMSANERASYMLQSMSEADTRIQLLQPDGMMFLDSNGFSDNRTIRTPDVVRAAEGDTSAWIGKDETSGERIVAASAPLLREGRIISVVRYSAALGEVDRMVTLLIRMTLLTGAAVILLFLALSMWMAGRIVRPLRELTRRARHMAAGDWQLGMSGQRGRDEIGQLSDTLHTLAVELNKREKLKNDFISSVSHELRTPLTSIKGWSETLADPGSRREEVQEGLGIIARETERLTGLVEDLLDFSNLSSGSMDLHLEELDLNLPVRECVTQQAVRQEETGVRLLSLLEPAPLLVRGDPNRLRQVLINLIDNAFKFTPEGGSIRVSAHREGAEAVLLVADSGVGIAPEDLPHVTDKFYKGLSARPGSGLGLAICKEIAEQHGGSLHIGSEPGAGTTAELRLPLIDGSGPLLPG
>NZ_CP045802.1|WP_028598694.1|4952844_4953189_+|hypothetical-protein
MSRLDMELCPRFEKAVDLLSKRWTTLIVYKLLAGPQRFARIEDSLPGLSGKMLAERLKELEAEGVVLRTVYPEMPVRIEYSLTDKGRALEPIVSEIARWSQDWLPASSPDPAES
>NZ_CP045802.1|WP_153784283.1|4951840_4952662_-|alpha/beta-fold-hydrolase
MEKQLILRHEGLELTATLHYPAASAADERERQPVVVICHGFIGSRIGVDRLFVKTARALAAQGSFVLRFDYGGCGESSGSYGALGFDSMIGQTRAALDYVLAMDCVDPQRVTLLGHSLGGAVALHAAVKDKRVNRLILWSAVGYPFNDIVRLVGRSGYDEAVLKGSTDHAGYTLEPKFFDSLQQHQPFQAAVRFGGDVLLVHGTSDDVIPADYSFLYQKVFWTRGDGLCDKEILFQADHTYSTRAHQEEAIRVTVDWLAKLEKRHEQWLDWSI
>NZ_CP045802.1|WP_028598696.1|4950658_4951801_+|hypothetical-protein
MRRLRLIAAAALLLLLAGCKGSKTNNELYLKAIGIDYKDGIYTMYVQMLDFAGESKSETGTVSGKQIPIWTGHGSGKSIGDANAKLMNSSQQPMDFSHVSALLLTEGALKAMSSRDISELIAGYPESRMNVWMFGTRHKLDDIFITKSFFNLSNTTTLLHSPEASYSQKSDIEPVFLFKLLRELQHPAINGYVPELMLEERAWEKDEKPHPELKVAGAFFFRQAAYETRLPIGQLEGWHWMNPHMEQYLIEIVHDGVDYGYGSFTRTKIKLRLKEDEQGEPAFEARVHVKGVLMTRNTQSPMAEVEEAAAKMIEAQIVSTYRSALSRKIDIFELEELYYRKHPREWQERTDGGAKTLLKPDSLRLAEVRVDLESPGKYKP
>NZ_CP045802.1|WP_153784282.1|4948969_4950646_+|spore-germination-protein
MKKPNANRAAGTATACGNGGSAGNSAGNGGSEGERLPGREQLRQWLQGSDDVSLLDIEVEAERARPGAEAQASEAPDEVDEAEKPPRGLPEPGPPSGARPLKLTLVYCSAMADPMLLQKVVLPQARAGVPALAPEEAASARPGNMGAWQELKLPRISKEAPHTITWRDYICRMIFEANAILFCDEQQRAWSMSAGTVPGRSPSEAATEVSVRGPKDGFVEQLHTNTALIRYRLRTPGLRCEQLCVGTRSGTKAALLYEADIANPQLVDAIRDKLSGIDADDIVSTRHLQDLLVDRSWSLLPRTSYTGRPDFAVQCLAAGRAVILLDGNPTAIIAPANLFLLMKSAEDAQQNYFFVNFTRLLRYVCLLVTCFLPGLYIALAVYHVDQIPFNLLATIMNSRLGLPLSSIEEMFLALLLIEIFREAGARLPGAIGQTLTVVGGLIIGDAAVRAGLISPVMIVMAAMTFVAGSTLVNQSLTGAVTLIRFYVYASSSALGFFGFMISTISVLVYLTRIQSFGVPYLTPISPIQLRDLLPGLFILPFRKRPRRAEALRVQKPLK
>NZ_CP045802.1|WP_084137135.1|4947782_4948973_+|GerAB/ArcD/ProY-family-transporter
MPAPIHTSRMGRRRPSDPRHARKEARNPMPISNRISVWTCIIMLLLSSGGVANILVPPFIFSRSGSDSWVAILLALPPMLLWCGLLCYVIRKLNGVPIEQWLSDRFGRAASWTMRALVVVLLLLQASTLSWETAHIAIHSYMSHTPVWIIAGATAALCAWTASGGLRSIAYACVILVPIAVILDSLLLMLNWPNMDSRMLLPILENGISPALKGMPLAAAAMLEIWLVLFVQQHVKGRFRWYQFALLVLFLCWLQLIPVVVSICVFGSDQAFKLRSPVLEIWKVISLGPTIEHIDLFAIVQRVSSTFARISLLFYLSARLGPVRGRRGLTIFFVGMAAVVTAFSSSKVTDSELFFFLIEYQYPVFIAFVPALTALLAILLRWRSPLPTAGKEAEPG
>NZ_CP045802.1|WP_153784287.1|4960517_4961411_-|ABC-transporter-permease-subunit
MSAASPSPVEPAARAAASALPSAASRRLVVSALRFVLTAALALLTVGPLLYLLAQIFMTPAEASMYPPRLLPSGLDTSSLRQAIETVPIFGFIANSFVLASAVTALQVLSAALAAYAFVYVRFAGSRFWFALFISTMMIPWEVTIIPNYLTVKSWGWLDTFPGLIVPFAASAFGVFLLRQFFLQLPRELFEAARIDGCGHVRHFLSVVLPLSGPAAASLGVYVFLNGWNMYLWPLLVTSSDAMRTVQIGIAMLQFEEMTSWNLVLCGVALVLVPSLVLLALGLRPLVRGITAGAVKG
>NZ_CP045802.1|WP_153784796.1|4961407_4962352_-|ABC-transporter-permease-subunit
MSGASSHLASGAASPRGAARSARLRRWREQALGYAFLAPSLAVFAVFLFYPMIRSVYLSFQLTDPRGRVAAYAGWDNYTGMLQSSAFWNSLLVTLKFTLLTVPAGLALGLLCASLVHSAGRGRSALRFLFSLPLAMSVSTASIIWMILYHPSLGMLNWLLLQLGLGPVQWLTDPGSALGSVSLMTVWMNSGFPFVLLLAAIQGLDGDVLDSARIDGASGWRTFVSVKLPLLSPTLFFLAVVSVMSAFQSFGQIHILTKGGPAGSTDVLVYSIYREAFVNYQFGTGSALAIVLFAIMLLLTLLQFLVLGKKVHYQ
>NZ_CP045802.1|WP_153784288.1|4963811_4965092_-|phosphoribosylamine--glycine-ligase
MRILVIGGGGREHAIVWSLAKSPKVSELLCAPGNAGIAELAECVPIAVDRFDDLVQLAREREIDLVFVGPDDPLAAGIVDAFQDAGIPAFGPDRKAAEIEGSKIFMKDLLRKYDIPTARYESFTDFEAALAYLRTQQAPIVVKADGLAAGKGVTVAATLEEAEEALRGMMLGGVFGASGSQVVIEEFMTGEEMSILAFVDGETVRAMVPAQDHKPIFDGDKGPNTGGMGTYSPLPHLSEALVNDAIATIIEPTARAMVAEGRPFRGVLFAGLMLTPDGVKTVEFNARMGDPETQVVLPRLETDLLDIVLAAMDGRLADIEIKWKDEAAVCVIAASEGYPGSYPKGRPISGLEAAKEAGALVFHAGTAEKDGEIVTSGGRVLGIVGLGRDIAEARERAYEAADRISFEGMQRRSDIAMKALKAAGQA
>NZ_CP045802.1|WP_101808211.1|4965313_4966861_-|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase
MAIRRALISVSDKTGIVAFARELADAGVQIISTGGTHGLLEKEGIPVIGISEVTGFPEIMDGRVKTLHPAVHSGLLAVRDNEEHQRAIRELGLDYIDLVVVNLYPFAATIAKPDVTYEDAIENIDIGGPTMLRSAAKNHAFVTVVVDAADYEGVLSEIKQDGDTTLDTRKRLAAKVFRHTGAYDALIGDYLSKLGGDPLPERYTVTYEKVQDLRYGENPHQRAAFYRRPLAEAGNVTTAEQLHGKELSYNNINDANAALAIVKEFSEPAVVAVKHMNPCGVGVGADIHEAYQKAYAADPTSIFGGIVAANRTIGAETATLLSEIFLEIILAPDFTPEALDILSRKKNIRLLRTGELAAAAGRKSDWVVTSVEGGMVVQESDVHSISEADLKVVTERQPTAEEMKQLLFGWKVVKHVKSNAILLAKDDMTVGVGAGQMNRVGAARIAIEQAGEQAKGAALASDAFFPMGDTVELAAKAGITAIIQPGGSIKDEESIRAANEHGIAMVFTGVRHFKH
>NZ_CP045802.1|WP_153784289.1|4966897_4967593_-|phosphoribosylglycinamide-formyltransferase
MAEQLRFDLGDGDRTGGQLRVAVFASGQGSNFQALADAAADGKLGGSIELLVCDRAEAPVVGRARRAGIDAWVFDPKAYASREAYEGEILAELQRRGVGLVVLAGYMRILTPVLVDAYAGRMINIHPSLLPAFPGMHAIRQALNYGVKVTGVTIHFVDGGLDSGPIIAQRALEIGEGESEASLAERIHAAENALYPWAVRGFAEGRISLDGRRALVSADAGAGADDDSADK
>NZ_CP045802.1|WP_153784290.1|4967592_4968636_-|phosphoribosylformylglycinamidine-cyclo-ligase
MAEAYKQAGVDIAAGNEAVERMKKHVKRTIRPEVLGGLGGFGGLFSLDKNKYEEPVLVSGTDGVGTKLMLAFAMDKHDTIGIDAVAMCVNDIIVQGAEPLFFLDYLATGKVEPEKIEQIVAGIAEGCVQAGCALIGGETAEMPGMYTPEEYDIGGFTVGVVDRAKMIDGSAIAPGDAVIGLASSGIHSNGYSLVRRLLLEQAGYGLQDELAELGGKRLGDVLLEPTRIYVKPALELIGKVQVKGMAHITGGGFIENIPRVLPEGVNVEVAFGSWPIQPIFKLLQDKGSITNRDMFTTFNMGIGLVVVVPADEAEAALAALAELGEQAYRIGAVTEGSRIVTFTGADV
>NZ_CP045802.1|WP_153784797.1|4968665_4970132_-|amidophosphoribosyltransferase
MRAVSRAWEDAHYNAGIGRDDIFDKLKEECGVFGVFGTPDASSLAYYGLHALQHRGEESSGVCTVDSATGGFAYHRGMGLVKEVFTSDILASLPGDRAIGHVRYSTSGASQLGNAQPLVFKYRDGDLAVATNGNIVNAPSIRRELESMGSIFQTTSDTEVIAHLIARSPKDFVSAARDALRRIVGGFAFLIMTNERLLVASDTNGLRPLVMGRLGDGYVFASETCAFETIGAEYVRDVQPGELLILDADGLREERFDEEERRASCAMEYIYFARPDSDINEVNIHTARKQMGRRLAVEAFVDADIVVGVPDSSISAAIGYAEQTGIPYEMGLIKNKYSGRTFIQPSQELREKGVKMKLSAVRKIVQGKRVVMIDDSIVRGTTSLRIVNMLREAGAAEVHVRISSPPFANPCYYGIDTPDRRELIASSKTVEEIREAINADSLYFLSAEGLIESASVPGDSKGGGLCLACFNNDYPTPVDESSDKSCSC
>NZ_CP045802.1|WP_153784291.1|4970278_4972528_-|phosphoribosylformylglycinamidine-synthase-subunit-PurL
MTQQSTAKALEPTAEQIAEQRIYQQFGVTDHEYELICGFMGRLPNYTEIGVFSVMWSEHCSYKNSKPILKKFPITGPKVLMGPGEGAGIVDIGDNQAVVFKIESHNHPSAVEPYQGAATGVGGIIRDIFSMGARPVALLNSLRFGRLESDRVKYLFEHVVGGIAGYGNCIGIPTVAGEVMFDESYEGNPLVNAMCVGLIDHDKIQRGVAKGVGNPVFYVGPATGRDGIHGATFASVELSEESEEKRTAVQVGDPFMEKLVMESTLELIDSGIVLGIQDMGAAGLTCSSAEMASKAGNGLELYLDEVPQREEGMTPYEMMLSESQERMLFVVAPEHEAQAREIFERWGVICAKVGKVTDDGRLRLFHQGEQVADMPVKALVDECPVYSKPSQEPASYAASASIDTAAFEEITDLTGALKDVLGSPTVASKEWVYRQYDYMVRTGTAVPPGSDAAVVLVPGTRKALAMTTDCNGRYVYLDPEVGGAIAVAEAARNIVCSGAQPLAITDNLNFGSPEKPEVFWQLEKAADGMSEACRVLETPVIGGNVSLYNENAKGAIYPTPVIGMVGLIDDIDYITTQEFKQAGDAIILLGETRAEFGGSELQQVRGGKAEGRPPALDLAVEKTLLDAVQAAIRAGLVASAHDLSEGGLAAALAEASFGRGLGASVDVATELRADHALFSESQSRILLSASPERKGELLALLAERGVPHAELGTVGGEELDIRVNGRPGVRAAVSELRSVWKEAIPCLMK
>NZ_CP045802.1|WP_028598682.1|4972505_4973201_-|phosphoribosylformylglycinamidine-synthase-subunit-PurQ
MKFAVIVFPGSNCDIDCYKAVEETIGQSVDYVWHTATDLSAYDAILVPGGFSYGDYLRCGAIARFAPVMAEVVKAAEAGKYVLGICNGFQILTEAGLLPGALLRNRDLKFLCHQSPLEVVNAATPFTNQYREGEVISIPIAHGEGNYYCDDETLARLQKNNQIVFRYASGGNPNGSVHDIAGICSERGNVVGMMPHPERAVSQLLGSEDGKRMFTSILNAWREQHDAAVNS
>NZ_CP045802.1|WP_028598681.1|4973205_4973448_-|phosphoribosylformylglycinamidine-synthase-subunit-PurS
MKATVYVTIKQNVLDPQGTAVQGALHSMGFAEVDKVRIGKYLELTLDTTDRAEAEERVRAMCEKLLANTVVEDYRFELEG

Crispr_ID: NZ_CP045802_22

• CRISPR_ID: NZ_CP045802_22
• CRISPR_location: 5087743-5087904
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP045802_22

Consensus_repeat	Method
GTTTCAATCTACGCTCCCCAGCGGGGAGCG	CRISPRCasFinder

spacers of NZ_CP045802_22

>22.1|5087773|36|NZ_CP045802|CRISPRCasFinder
CGCGCGGGACTACCATTTGAATGTGATCGGGCTACC
>22.2|5087839|36|NZ_CP045802|CRISPRCasFinder
ACGTTAGCCGGGGCCCCTCGGTTATTTTCCAGATTT

CRISPR arrays and Neighbor proteins around NZ_CP045802_22

CRISPR arrays

The CRISPR arrays of NZ_CP045802_22

>merge|NZ_CP045802|22|5087743-5087904|CRISPRCasFinder
GTTTCAATCGTCGCTTCCCTGGGGGAGACGCGCGCGGGACTACCATTTGAATGTGATCGGGCTACCGTTTCAATCTACGCTCCCCAGCGGGGAGCGACGTTAGCCGGGGCCCCTCGGTTATTTTCCAGATTTGTTTCAATCCACGCTCCCCAGCGGGGAGCG

>NZ_CP045802|22|18|5087743-5087904|CRISPRCasFinder
GTTTCAATCGTCGCTTCCCTGGGGGAGACG	CGCGCGGGACTACCATTTGAATGTGATCGGGCTACC
GTTTCAATCTACGCTCCCCAGCGGGGAGCG	ACGTTAGCCGGGGCCCCTCGGTTATTTTCCAGATTT
GTTTCAATCCACGCTCCCCAGCGGGGAGCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_043111208.1|5097923_5098625_-|sulfite-oxidase-like-oxidoreductase	unknown	unknown	gnl|CDD|239027
NZ_CP045802.1|WP_153784360.1|5083851_5084739_-|ABC-transporter-permease-subunit	unknown	unknown	gnl|CDD|223472
NZ_CP045802.1|WP_052333153.1|5097293_5097743_-|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_CP045802.1|WP_153784355.1|5074779_5075373_-|DUF4309-domain-containing-protein	unknown	unknown	gnl|CDD|372945
NZ_CP045802.1|WP_153784364.1|5094667_5095495_-|hypothetical-protein	unknown	unknown	gnl|CDD|274875
NZ_CP045802.1|WP_153784358.1|5078254_5080072_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|227095
NZ_CP045802.1|WP_153784362.1|5087069_5087654_-|VOC-family-protein	unknown	unknown	gnl|CDD|319910
NZ_CP045802.1|WP_153784359.1|5082079_5083759_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270300
NZ_CP045802.1|WP_153784357.1|5076260_5078090_-|cellulase-family-glycosylhydrolase	unknown	unknown	gnl|CDD|365907
NZ_CP045802.1|WP_153784365.1|5098630_5098864_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153784363.1|5093314_5094607_+|C4-dicarboxylate-transporter-DctA	unknown	unknown	gnl|CDD|234968
NZ_CP045802.1|WP_153784361.1|5086265_5086889_-|uridine-kinase	unknown	unknown	gnl|CDD|235492
NZ_CP045802.1|WP_153784802.1|5080071_5081859_-|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|225519
NZ_CP045802.1|WP_028598637.1|5088024_5089104_-|DctP-family-TRAP-transporter-solute-binding-subunit	unknown	unknown	gnl|CDD|270392
NZ_CP045802.1|WP_028598647.1|5084757_5085726_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|226666
NZ_CP045802.1|WP_028598634.1|5091812_5093258_+|NAD-dependent-malic-enzyme	unknown	unknown	gnl|CDD|223358
NZ_CP045802.1|WP_043111209.1|5089276_5090899_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225827
NZ_CP045802.1|WP_153784356.1|5075440_5076235_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028598635.1|5090885_5091587_+|response-regulator	unknown	unknown	gnl|CDD|226931
NZ_CP045802.1|WP_028598631.1|5095600_5097229_-|MFS-transporter	unknown	unknown	gnl|CDD|129794

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_043111208.1|5097923_5098625_-|sulfite-oxidase-like-oxidoreductase	gnl|CDD|239027	cd02109, arch_bact_SO_family_Moco, bacterial and archael members of the sulfite oxidase (SO) family of molybdopterin binding domains. This molybdopterin cofactor (Moco) binding domain is found in a variety of oxidoreductases, main members of this family are nitrate reductase (NR) and sulfite oxidase (SO). Common features of all known members of this family are that they contain one single pterin cofactor and part of the coordination of the metal (Mo) is a cysteine ligand of the protein and that they catalyze the transfer of an oxygen to or from a lone pair of electrons on the substrate. The specific function of this subgroup is unknown.	1.56751e-97
NZ_CP045802.1|WP_153784360.1|5083851_5084739_-|ABC-transporter-permease-subunit	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	2.46818e-54
NZ_CP045802.1|WP_052333153.1|5097293_5097743_-|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	3.44731e-23
NZ_CP045802.1|WP_153784355.1|5074779_5075373_-|DUF4309-domain-containing-protein	gnl|CDD|372945	pfam14172, DUF4309, Domain of unknown function (DUF4309). This family includes the B. subtilis YjgB protein, which is functionally uncharacterized. This is not a homolog of E. coli YjgB. Expression of B. subtilis YjgB is regulated by the alternative transcription factor sigma-B. This family is found in bacteria, and is approximately 140 amino acids in length.	4.76076e-29
NZ_CP045802.1|WP_153784364.1|5094667_5095495_-|hypothetical-protein	gnl|CDD|274875	TIGR03951, Fe_III_red_FhuF, siderophore-iron reductase FhuF. Members of this protein family, including FhuF of E. coli, are siderophore ferric iron reductases that appear to play a role in iron removal from certain hydroxamate-type siderophores, including coprogen, ferrichrome, ferrioxamine B, and aerobactin. Genes occur in regularly in siderophore transport and/or biosynthesis clusters. The C-terminus includes four Cys residues in a C-C-10(X)-C-X-X-C motif that binds a 2Fe-2S cluster. Family TIGR03950 is similar, but especially in the C-terminal region, but likely acts on a different panel of siderophores. [Energy metabolism, Electron transport, Transport and binding proteins, Cations and iron carrying compounds].	2.86114e-06
NZ_CP045802.1|WP_153784362.1|5087069_5087654_-|VOC-family-protein	gnl|CDD|319910	cd07246, VOC_like, uncharacterized subfamily of vicinal oxygen chelate (VOC) family. 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.	3.96144e-25
NZ_CP045802.1|WP_153784359.1|5082079_5083759_-|extracellular-solute-binding-protein	gnl|CDD|270300	cd13582, PBP2_AlgQ_like_3, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	3.52173e-62
NZ_CP045802.1|WP_153784357.1|5076260_5078090_-|cellulase-family-glycosylhydrolase	gnl|CDD|365907	pfam00150, Cellulase, Cellulase (glycosyl hydrolase family 5).	4.7796e-24
NZ_CP045802.1|WP_153784363.1|5093314_5094607_+|C4-dicarboxylate-transporter-DctA	gnl|CDD|234968	PRK01663, PRK01663, C4-dicarboxylate transporter DctA; Reviewed.	0
NZ_CP045802.1|WP_153784361.1|5086265_5086889_-|uridine-kinase	gnl|CDD|235492	PRK05480, PRK05480, uridine/cytidine kinase; Provisional.	6.46622e-107
NZ_CP045802.1|WP_153784802.1|5080071_5081859_-|HAMP-domain-containing-protein	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	2.92058e-49
NZ_CP045802.1|WP_028598637.1|5088024_5089104_-|DctP-family-TRAP-transporter-solute-binding-subunit	gnl|CDD|270392	cd13674, PBP2_TRAP_SBP_like_1, Uncharacterized substrate-binding protein of the Tripartite ATP-independent Periplasmic transporter family; the type 2 periplasmic-binding protein fold. This subfamily includes uncharacterized periplasmic substrate-binding proteins similar to TRAP transport systems such as SiaP (a sialic acid binding virulence factor) and TeaA (an ectoine binding protein). TRAP transporters are a large family of solute transporters ubiquitously found in bacteria and archaea. They are comprised of a periplasmic substrate-binding protein (SBP) and two unequally sized integral membrane components: a large transmembrane subunit involved in the translocation process and a smaller membrane of unknown function. The driving force of TRAP transporters is provided by electrochemical ion gradients (either protons or sodium ions) across the cytoplasmic membrane, rather than ATP hydrolysis. This substrate-binding domain belongs to the type 2 periplasmic binding fold protein superfamily (PBP2). The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	3.28246e-138
NZ_CP045802.1|WP_028598647.1|5084757_5085726_-|sugar-ABC-transporter-permease	gnl|CDD|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	6.45105e-111
NZ_CP045802.1|WP_028598634.1|5091812_5093258_+|NAD-dependent-malic-enzyme	gnl|CDD|223358	COG0281, SfcA, Malic enzyme [Energy production and conversion].	0
NZ_CP045802.1|WP_043111209.1|5089276_5090899_+|sensor-histidine-kinase	gnl|CDD|225827	COG3290, CitA, Signal transduction histidine kinase regulating citrate/malate metabolism [Signal transduction mechanisms].	0
NZ_CP045802.1|WP_153784358.1|5078254_5080072_-|helix-turn-helix-domain-containing-protein	gnl|CDD|227095	COG4753, COG4753, Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain [Signal transduction mechanisms].	9.53867e-43
NZ_CP045802.1|WP_028598635.1|5090885_5091587_+|response-regulator	gnl|CDD|226931	COG4565, CitB, Response regulator of citrate/malate metabolism [Transcription / Signal transduction mechanisms].	3.24028e-81
NZ_CP045802.1|WP_028598631.1|5095600_5097229_-|MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	1.03312e-53

Protein sequences

>NZ_CP045802.1|WP_153784362.1|5087069_5087654_-|VOC-family-protein
MCRAAVPQRGSGHPASIITRGGIRVDHNVSTSGVTGEHTTNGRPHGYSALTPFIVVSDPAEAIRFYEAVFGAKTKSVTDVGTDGNSFIVHADIDFGNGYLQLGAANPDYHLVPPPGGGDACYSLGVYVPDVDRALELAVQHGATVREPAANFVSGDRYCSILDPFGIRWSIMTRVEDLSEEESARRVAEWSKSL
>NZ_CP045802.1|WP_153784361.1|5086265_5086889_-|uridine-kinase
MLIIGIAGGTGSGKTTVARSVIERMGTGNVTFISQDNYYRDRPELTFAEKEKINYDHPFAFENELLVEHLQQLKRGVAAEAPVYDFTMHARKSDETVTLLPSSIVMIEGLHVLSDEGLRGLLDIKVFVDTDPDVRILRRVLRDIEERGRSIHSIHDQYMQTVKPMHEAFIEPSKKYADLIIPEGGHNEVGIGVLASLTEKYLSSGHY
>NZ_CP045802.1|WP_028598647.1|5084757_5085726_-|sugar-ABC-transporter-permease
MEPGAQAGIEAASPKAGSERWKKWLRRIYSQRYLQVMALLGVAWMVVFNYIPMYGIIIAFKEYDIIFPMSMAPWVGLDNFREFLSDDMLLTVIKNTLGISLIKLIIGFPLPILFALLLNEVRSVMFKRWTQTITYLPHFLSWVILGGILATWLSDVGIINKILLSLNVIDAPITYLAEPKYFWSIIIVSDIWKELGWSAIIYLAAISSVSPELYEAATIDGAGRLQKMRNITLPSIMGTITILFILAVGNVLNSNFDQILVLRNQLNAEASTVIDYYVYQTGLIDNRFSYSTAVNLIKSVIALFLLLMANFVTKKLNNNSLF
>NZ_CP045802.1|WP_153784360.1|5083851_5084739_-|ABC-transporter-permease-subunit
MFSLKRQTPGEAAFGILNGLLMLIICFLTLYPIWYVLVNAFNDGADAMRGGIYWIPREFSLENFRAVFRSEGIMTAMGVTVAKTLVGVPVHVLFTAMVAYAVSRRELIGRNLYMIIGTITMFFGGGLIPYYLLIRDLGLLDNFLVYIIPAAFSFFDLIIFLSFFREIPAGLEEAARIDGANDLTIFTRVIIPVSMPVVATIALFHGVYQWNDYFTGMIYINNTDLQPIQTFLYRVVAQSSSNQMLGAMPSGVTQTVTSQSLKLATMVVTTAPIVCVYPFLQKYFVKGFMVGSLKG
>NZ_CP045802.1|WP_153784359.1|5082079_5083759_-|extracellular-solute-binding-protein
MRTTRKVATTLLALAMTFSVAACSSNGNGNSNSGGTASPAPTAGTDASASPAPAASDEPAWKQDTSPITFDWYLNFSWFNKKWGGDATADYITKKTGVSLNFIVPAGNENEKLNTLMASGSLPDFITLGWYEEGVRKMIEGKLVLPLNKLAEEYDPYFFKVGDPAKLGWYTKEDGNVYGYPNASSSPADYEKYGENFTSNQTFAVRKDMYEALGKPDMSTPEGFLNALKLAKEKFPDVNGQPLIPLGLHEFTETGNYSLEGYLQNFLAIPQVKDGKLYDRRQDPEYLKWLKVFRQANQDGLLAKDIFIDKRPQMEEKIAQGRYFAMLYQRSDFAAQNTQLYQKDPNMVYIAVDGPKNAAGDQPTLSGPGISGWTVTLISKNVKDKKRAIAFLSYLMSEEGNKDLFLGEKGVTYDTIDGKDQFLPEALELLNKDRTAFDQKYGASFTYWMLMDTNMNLQWAPPSVEPAKQMEDWTKGKSISMAEFDNLDPAATSKEGVAGSKNARAWGKALPKMILAKSDAEFDEIFNKYLKDRSEQEAIDAYRQAAYESNLKKLESLNK
>NZ_CP045802.1|WP_153784802.1|5080071_5081859_-|HAMP-domain-containing-protein
MLLFSWYTLHGVSDYSMRELVKKNESILDIERTNIQNNIELMEWTGQLALSNREMNDYLQTKEDLDTEWLLDFKTRTFQMFQSFLFNNPRISGIRLFASNPEVHEFWPIVLSEARIRDKPWYDTVLDRKGLVWWEIQNNRELLNNTSTTSGSEVMSVSLLREFKYPDDMTHNGLLEISMELRNFFTKTFSSVQDPSSRMVVVDRRGQVHADMAAPIFQQTPAKELLRHIALTEAPGNHTSYFTAGGQSFLAIQAFIPGLDAHLVNLVSRTDTLADIERTRGNLVILIVVLIAVLILLSYFMQSIILKRLRVLRDSMKKVRGGDFHVDVPVAGSDEVGELAHHYRQLLRKINELIVDQVNRQAAGKEAELRSLKNQIDSHFLYNTLENLKMLAEIEGQYTISDALTSLGGMMRYSLQWTRGHVRLKDEVQHIQNYIAIMNIRYDGKLELRLDIAPECLEQEVLKMSLQPIVENAVKHGMDDLDSDSGKLTITVSAFIRLDDCVIEVTDNGCGIPGEQLRLLNGMMRMEEADYQERRARTSAARRGEGSGIGLRNVDHRLVMSYGQEYGLRVESVEGSFTKVVMTLPHLILTGGEPR
>NZ_CP045802.1|WP_153784358.1|5078254_5080072_-|helix-turn-helix-domain-containing-protein
MRNLLIVDDEKNIRLGLKAMIERQFPGRYAFRFAENGREALEQLAASPADLMITDIRMPVLDGLGLLERLHALGRGTGGGADRAAAGAQGESGRGDRAAAGAQGESGRGDRAAAGIQGESGRGDRAAADASEREAAGGSERGAAGSPDPAAQGKLPASPAARPLAGPAPLVIILSGHDDFPYARAAIRYQAKEYLLKPIKREELFEVLERLEGELDRRHGAAAGAAAPADRESRAGELLQGMLAGEAAPEAAALAAAGLGWLAGDYSVGVLRAAGGGEGSQLQGLVQPLLEETGSEAWAMRQLRGGDLVLAAEDEELLRRLGARLDGHALLRCRLALSSRASGPGQLRRAYSQAQQAQKYFLLHPGVALLSYDSVRSLSAGCPLPEEPIRRLSNLLGTGRLPEMKKLLQGILDIRVIGRCEIGYLEGISRRLNEEVFDGVFRSYGEESVDILRLYKNAGHIENFERFEDYYRHAEQLLERLDEFVGRVRGAHADRKDMQKAVEYLLEHYAEDVNMAVVSNHISLNYTYFSQAFKEHTGESFSSYLRKLRLNRAKDLLSSSDLKVYEISAQSGFDNVKHFTRVFKEAEGITPLEFRSMRQGIGPGR
>NZ_CP045802.1|WP_153784357.1|5076260_5078090_-|cellulase-family-glycosylhydrolase
MATENGCRQSEVDGWVKADGKRLVNGRGEELILRGVGLGSWLLPEGYMWKMPQQGDRPRRIEAMVSGLLGESGAEAFWRTYFERYTAEEDIRQLALEGFNSVRVPFNSRKLLEGPLNEDGYNAFQVGLLDDVVGWCRKWGVYVILDMHGAPGGQTGANIDDCENDQPELFTSAEHRQASIDLWRYLAKRYRDEWIVAGYDLLNEPLPEFHGQYNDRVEPLYRDMIAAIREVDDRHLIVVEGVHWSTDFSIFTEKLDGNVLYQFHKYWNNPDTESIQKYLDFRDEWNVPIFMGEGGENDLDWYAGGFRLFEDHRIGWNFWTWKKMDTTNSPCSVRKPDGWEKLGAWLEGGAKPEPEEAVRILGDYLDGLPLAAVDYRPEVVNALLRRLPVRIPAIHYGYKGEGESFGLGGAERIDWESGYRRGDGLAIRKLDGAPHLPPSEPGWHPWNVGDGLCVELPAGAWTAYEFLAPDAAADAARAGSAAAGAARANAAATGSAATPDGGAQASDEAAAAADSAGGVGREAAVMDLDVGAQESGEAAGFGVKLRLKAAAAGAAAELELDGRPIGRLDASGEWSEAELGALPQPEPGLRRLVVKASGGALLLEGIWLG
>NZ_CP045802.1|WP_153784356.1|5075440_5076235_-|hypothetical-protein
MDKASRPASAQGGTLYNSLPVQPPSVEASQGTLDSLVGRKPRIPALQGTPGSLAEPKPRIPAIEGTLDSLAEPKPRIPAIEGTPGSLAEPKRRIPAIEGTLDSLAEPKPRIPAIEGTLDSLAEPKPRIPAIEGTLDSLVEPKPRVPAIQGTLDSLAEPKPRIPAIQGTLGSLDEPHPRIPAIEGTLYSLAEPKPRIPAIQGTLGSLAEPKPHIPAIEGTLRSLDEPHPRIPASQGTLDSLIKPRLCNLSAARSVWIYASLIIYI
>NZ_CP045802.1|WP_153784355.1|5074779_5075373_-|DUF4309-domain-containing-protein
MKANAKKAALSVLAAAVVAGFGASLPQEAAHAAAKPAAAASASDQKMAMEKLMAMYKPALEGQFPNFNGFTIGKTTRQQVIDQLGEAPEPRKTAGGFDFYHAEMGHPGYALRYDRDNVVAEMRYFGTNVERQTNIGGMTRDLLVQQWFMPQASTVFTSGGKKQKKLSYVRGNYQLDFIFNDVKGTDLDHINLIPKAL
>NZ_CP045802.1|WP_028598637.1|5088024_5089104_-|DctP-family-TRAP-transporter-solute-binding-subunit
MGKWRFKLWGGGLLLAAAAVLTIFWLGGYKLPGPLPVDDEQTGFSGRHVIKFSYVVAENTPKGLAAQRFADLVEEKSGGKVQVQLFPNGTLYTEPDEQAALARGDVQMIAPAFSNLSTRMPEWSVMDLPFAFPTEKAVEEAFGGEVGSMLFKRLESRGMIGLAFWGNGFKQMTASDRPLEHPQDFRGLKFRILPSPIIDAQFRSLGAATADIPFNSVYKAFESGTVDGGENTITNIYSKKFYQVQNYMTVSNHAYLGYAVVMNLSFWESLPSDVQGIIQEAMRETTGWANESAREMSRKELAEMRSGRLMSIIDLGEAERREWMDLWEPLYGQAEKLAGRELMDAVRRLRSKYESQGGE
>NZ_CP045802.1|WP_043111209.1|5089276_5090899_+|sensor-histidine-kinase
MLKQLKINWKIALLSFGVVLFALAAGGGVAVGSILHLQEKELGRRLLVTAKTAASLPVIVAGLEDAALQPKLREAAEKIGIIHDATYVVVLDMQHKRLSHPVPDRVGTFSRGTDEGPAFAEHSYVSKAKGELGTALRAFVPVMDSMHVQIGTVLVGRVLPSPREVILPFAGQISTVLLLSLLVGLAGSWALARQIKKEMFDMEPLEIARLLMERDATFHAMHEGVIAIHNDERIAVFNERARQIFHIGGDVVGRPIRDVLPDTRLPEILELDAPVYQQEIFIGGQHIVSNRVPIRVQGHTVGAVAIFQDRTEVARMAEELTGVKALVETVRVQNHEYMNRLHTIGGLIQLGQGEKALDYLFRMSDEREQLNRFLGTRFFHDSLTGLLLGKISRGRELGIDVRIDPHSRLQRFPKHLDHHDFVVLLGNLIENAFDSLASAPEPRRVLVSLEQDDEQLSMLVEDNGCGMDELVRQRMFERGFSTKPGDGRGIGMFLIAGIAEKGGGTIRVESAPGAGASITLSFPMTEESRPKKGRSEHEED
>NZ_CP045802.1|WP_028598635.1|5090885_5091587_+|response-regulator
MKRIKVVLIEDDPMVREVNRQFVESVEGFHVTGTASSGREGMELIRQMNPDLVILDIYMPGLDGIQTLRQLRSEGHAAGVIVISAANDRDTIRSMVQGGADDYIMKPFKAERVREALLRWRQRSRQLADGGQLDQGELDRFLHGPLSASASAPASDNGGSLPKGLQAATLEHILRYLALQEEAVSAESVAENVGIARVTARRYLEHLAKSGQLRLQLQYGLGRPVNLYSLDKS
>NZ_CP045802.1|WP_028598634.1|5091812_5093258_+|NAD-dependent-malic-enzyme
MSIPAGASTPIILRLELSRSTASFAQIATVIGDTGGDIVAIDVTRSDAASTVRDLTVNVYERSHADRIAAAVGRLPGVRVLQVSDQTFLLHIGGKIETTPKTPIKNRDDLSRVYTPGVARVCMAIHEKPSRAHTLTIKRNTIAVVSDGSAVLGLGNIGPQAAMPVMEGKAVLFKQFAGVDAFPICLNTQDTEEIIAIVKALSPTFGGINLEDISAPRCFEIERRLAEELDIPVFHDDQHGTAVVLLAGLLNAVKLTGKTLESCKIVVCGIGAAGTACSKMLMAAGVTNIIGVDREGALVPGKSYANEFWQWYADNSNPFRLEGSLSDVIEDADIFIGVSGPGVLKAEDLKKMAVDPIVFAMANPTPEILPEEAAPYVRVMATGRSDYPNQINNVLCFPGIFRGILDCRASRVTEEMKLAAAKAIASVVTDEELNEQYIIPSVFNHLVVERVREAVIEAAYASGVARKETPSKPRASSPTPI
>NZ_CP045802.1|WP_153784363.1|5093314_5094607_+|C4-dicarboxylate-transporter-DctA
MKINFRNLTVQVLTAIVIGIAIGYFFPSFGASLKVLADVFIKLIKMVITPIVFFTIVIGFAGMGSMKKIGRIGGKALLYFELVTTFAMAIGIAVAFLIRPGDGIDTSGVDSKSDAVAGYAQQASETSHGFKDFLLGIIPDNAIAAMASGQMLPVLFFSVLFGLALSMIGEKGRPVTEFFEKLNEIFFKIVGIIMRFSPYAAGGAMAYTIGKFGLGSLLSLGKMMVATYMTMFLFIIVILGLIARYYKFSIFGLIRHIKEEILLVLGTSSSESALPRLMNKMETYGCSKPVVGLVVPTGYSFNLDGTSIYLSMAALFIAQAYGIELTLLQILTFLGVLMLTSKGAAGVTGSGFITLAATLAALPGHPIPLEGIALLIGVDRFMSEARAITNLIGNSVATVVIAKSENQFQSSKEPGLAIGTAAGHSASVEA
>NZ_CP045802.1|WP_153784364.1|5094667_5095495_-|hypothetical-protein
MDEVIGVAQEAASFDFGIIKMYYHISPEGADEPLFEMDADRFFDAESLGGALDLGGATVQATSRALPASFVGTTIGKLLLTQAYLYAMYESILDLSPERLTFQVEAHDDHAHLGFRIKELLPQPVPSERAEELLAAAWTDYVRSFVRPAVEAVSEASGLKAAAIWQQYGAMSEYMKEFAGTMPLPEPVRERMALAFRVLAEGIPAEAFGTRRNPFVHKARYCDNPYPTGGDKLMMQSSCCLYDQREGGQKCYTCPMLTPEQRAERRVQVQAELAG
>NZ_CP045802.1|WP_028598631.1|5095600_5097229_-|MFS-transporter
MEHLTHKRKLSIMIAVMAAMFFAAINQTITSTAMPRIIAILDGMEYYTWTINIYLLTSTIATILVGKLSDMFGRKPFILAGILLFIIGAFLTGTSSDVYQFITYRGIQGIGAGIIQSTAFMAVGDLFSPRERSKWMGLMTAVFGFSSVLGPTLGGYLVDHLDWHWLFWIFLPLGVVAFAMIWVLFPKIERVKGEKIDLLGSLFLTTTIVPLLLGFSLAGPNHAWGSPEILGLFAAALVSGFIFVMVERYAKSPILPLHLFKNGIVTVSNLIGFLMNFGMMGALIYLTFFVQGVLGISATYSGYVTMPMSIFMVVTSALIGQRISKSGKYKRYALIGVPIMILGMGIMVLMNSVGMAVLSMCIFGIGIGMGMPVFSLATQNAVAHTELGVVTASSQLFRNLGGTIGIAVMGTVMSNTLTKNLKDTLTSPNMPDLSQLDPTVAQQLTGFANPNLLMNKPLIDETAAGLPEQARTLFLQLIEQFRGALGDTLALVFLVGTLVLCVSLVLVFFLREIPLRTTNQTAPAPAEGESAGAAAGKLQSES
>NZ_CP045802.1|WP_052333153.1|5097293_5097743_-|MarR-family-transcriptional-regulator
MKEEAKRFHAAVQAFIQTMEMSMPELLKECGMTRTQLFALHLVKVKGPCKLALIADKLEVKPSAVTVMMDRLESGGWVRRKPDTVDRRAVFVEITDEGRKALEKFQQLREKLIERRLVKLTVEEQRTLSGLMEKLAEDVPAEGQSAAEA
>NZ_CP045802.1|WP_043111208.1|5097923_5098625_-|sulfite-oxidase-like-oxidoreductase
MAQPYESDKAERLKRNAAALLQKIKPDAKYGDRVPPGQTVTDRFPILHEGAVPAYDMSTWDLRVTGAVREERRFSFAELESLPRVSVMRDIHCVTRWSKMDTVWEGILFRDFLRHLGIEPLPEAKHVMVYGDYDYETNVPLADLMGDDILLAFRYGGEPLTDKHGGPLRLVVPHLYFWKSAKWLRGFEFMTEDRPGFWERNGFHNEADPFREQRYSEEGFELPEDEWVHKDYD
>NZ_CP045802.1|WP_153784365.1|5098630_5098864_-|hypothetical-protein
MTERNESAEVQADGAAAEAEAQPKKMSLAEAAKLKLQQKKQTQAVGKQGQSGAQGGAKELRSQLNKKPNNQRRRMGV

Crispr_ID: NZ_CP045802_23

• CRISPR_ID: NZ_CP045802_23
• CRISPR_location: 5217743-5218132
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 7 spacers

Consensus repeat of NZ_CP045802_23

Consensus_repeat	Method
TGCAACCCGACTTTTTCGGGTTGCAGCTTGCCG	CRT

spacers of NZ_CP045802_23

>23.1|5217776|18|NZ_CP045802|CRT
GGCGCGCTCGCGGTCCTC
>23.2|5217827|18|NZ_CP045802|CRT
AGCGCGCTGCTGGGCTTC
>23.3|5217878|18|NZ_CP045802|CRT
AGCGCGCTGCCGAGCTTC
>23.4|5217929|18|NZ_CP045802|CRT
GGCGGGCTCGCGGTCCTC
>23.5|5217980|18|NZ_CP045802|CRT
CGCGGGCTGCCGGGCTTC
>23.6|5218031|18|NZ_CP045802|CRT
GGCACGCTCGCGGTCCTC
>23.7|5218082|18|NZ_CP045802|CRT
AGCGTGCTGCCGGGACTA

CRISPR arrays and Neighbor proteins around NZ_CP045802_23

CRISPR arrays

The CRISPR arrays of NZ_CP045802_23

>merge|NZ_CP045802|23|5217743-5218132|CRT
TGCAACCCGACTTTTTCGGGTTGCAGCTTGCCGGGCGCGCTCGCGGTCCTCTGCAACCCGACTTTTTCGGGTTGCAGCTTGCCGAGCGCGCTGCTGGGCTTCTGCAACCCGACTTTTTCGGGTTGCAGCTTGCCGAGCGCGCTGCCGAGCTTCTGCAACCCGACTTTTTCGGGTTGCAGCTTGCCGGGCGGGCTCGCGGTCCTCTGCAACCCGACTTTTTCGGGTTGCAGCTTGCCGCGCGGGCTGCCGGGCTTCTGCAACCCGACTTATTCGGGTTGCAGCTTGCCGGGCACGCTCGCGGTCCTCTGCAACCCGACTTTTTCGGGTTGCAGCTTGCCGAGCGTGCTGCCGGGACTATGCAACCCGACTTTTTCGGGTCGCAGTCTTGAT

>NZ_CP045802|23|6|5217743-5218132|CRT
TGCAACCCGACTTTTTCGGGTTGCAGCTTGCCG	GGCGCGCTCGCGGTCCTC
TGCAACCCGACTTTTTCGGGTTGCAGCTTGCCG	AGCGCGCTGCTGGGCTTC
TGCAACCCGACTTTTTCGGGTTGCAGCTTGCCG	AGCGCGCTGCCGAGCTTC
TGCAACCCGACTTTTTCGGGTTGCAGCTTGCCG	GGCGGGCTCGCGGTCCTC
TGCAACCCGACTTTTTCGGGTTGCAGCTTGCCG	CGCGGGCTGCCGGGCTTC
TGCAACCCGACTTATTCGGGTTGCAGCTTGCCG	GGCACGCTCGCGGTCCTC
TGCAACCCGACTTTTTCGGGTTGCAGCTTGCCG	AGCGTGCTGCCGGGACTA
TGCAACCCGACTTTTTCGGGTCGCAGTCTTGAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_153784408.1|5215390_5216236_+|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|224423
NZ_CP045802.1|WP_101807664.1|5213073_5213982_-|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|223566
NZ_CP045802.1|WP_153784405.1|5206620_5208018_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|274362
NZ_CP045802.1|WP_052333258.1|5223114_5224611_-|S41-family-peptidase	unknown	unknown	gnl|CDD|223864
NZ_CP045802.1|WP_153784406.1|5208605_5210084_-|HD-domain-containing-protein	unknown	unknown	gnl|CDD|225116
NZ_CP045802.1|WP_153784409.1|5216354_5217656_+|peptidylprolyl-isomerase	unknown	unknown	gnl|CDD|234605
NZ_CP045802.1|WP_043111322.1|5210246_5211107_+|aldose-epimerase	unknown	unknown	gnl|CDD|185702
NZ_CP045802.1|WP_028599044.1|5226886_5227804_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|225088
NZ_CP045802.1|WP_028599054.1|5211944_5212814_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|235853
NZ_CP045802.1|WP_028599057.1|5208285_5208504_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028599047.1|5224734_5225145_-|DUF86-domain-containing-protein	unknown	unknown	gnl|CDD|366864
NZ_CP045802.1|WP_153783988.1|5218245_5219505_-|IS256-family-transposase	unknown	unknown	gnl|CDD|307151
NZ_CP045802.1|WP_153784410.1|5220025_5221306_-|voltage-gated-chloride-channel-protein	unknown	unknown	gnl|CDD|239654
NZ_CP045802.1|WP_101807662.1|5221696_5223004_-|PDZ-domain-containing-protein	unknown	unknown	gnl|CDD|238487
NZ_CP045802.1|WP_084137297.1|5227793_5228486_-|cell-division-ATP-binding-protein-FtsE	unknown	unknown	gnl|CDD|225438
NZ_CP045802.1|WP_028599046.1|5225134_5225542_-|nucleotidyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|376187
NZ_CP045802.1|WP_084137302.1|5211241_5211898_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP045802.1|WP_153784411.1|5221304_5221700_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_153784808.1|5225680_5226811_-|peptidoglycan-DD-metalloendopeptidase-family-protein	unknown	unknown	gnl|CDD|366703
NZ_CP045802.1|WP_153784407.1|5214253_5215171_-|D-alanyl-D-alanine-carboxypeptidase-family-protein	unknown	unknown	gnl|CDD|350624

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_153784408.1|5215390_5216236_+|alpha/beta-hydrolase	gnl|CDD|224423	COG1506, DAP2, Dipeptidyl aminopeptidases/acylaminoacyl-peptidases [Amino acid transport and metabolism].	3.38602e-10
NZ_CP045802.1|WP_101807664.1|5213073_5213982_-|NAD(P)/FAD-dependent-oxidoreductase	gnl|CDD|223566	COG0492, TrxB, Thioredoxin reductase [Posttranslational modification, protein turnover, chaperones].	4.1039e-42
NZ_CP045802.1|WP_153784405.1|5206620_5208018_-|sensor-histidine-kinase	gnl|CDD|274362	TIGR02956, sensor_protein_TorS, TMAO reductase sytem sensor TorS. This protein, TorS, is part of a regulatory system for the torCAD operon that encodes the pterin molybdenum cofactor-containing enzyme trimethylamine-N-oxide (TMAO) reductase (TorA), a cognate chaperone (TorD), and a penta-haem cytochrome (TorC). TorS works together with the inducer-binding protein TorT and the response regulator TorR. TorS contains histidine kinase ATPase (pfam02518), HAMP (pfam00672), phosphoacceptor (pfam00512), and phosphotransfer (pfam01627) domains and a response regulator receiver domain (pfam00072). [Signal transduction, Two-component systems].	1.90778e-55
NZ_CP045802.1|WP_153784406.1|5208605_5210084_-|HD-domain-containing-protein	gnl|CDD|225116	COG2206, COG2206, c-di-GMP phosphodiesterase class II (HD-GYP domain) [Signal transduction mechanisms].	2.24007e-66
NZ_CP045802.1|WP_153784409.1|5216354_5217656_+|peptidylprolyl-isomerase	gnl|CDD|234605	PRK00059, prsA, peptidylprolyl isomerase; Provisional.	2.99196e-51
NZ_CP045802.1|WP_043111322.1|5210246_5211107_+|aldose-epimerase	gnl|CDD|185702	cd09025, Aldose_epim_Slr1438, Aldose 1-epimerase, similar to Synechocystis Slr1438. Proteins similar to Synechocystis Slr1438 are uncharacterized members of aldose-1-epimerase superfamily. Aldose 1-epimerases or mutarotases are key enzymes of carbohydrate metabolism, catalyzing the interconversion of the alpha- and beta-anomers of hexose sugars such as glucose and galactose. This interconversion is an important step that allows anomer specific metabolic conversion of sugars. Studies of the catalytic mechanism of the best known member of the family, galactose mutarotase, have shown a glutamate and a histidine residue to be critical for catalysis; the glutamate serves as the active site base to initiate the reaction by removing the proton from the C-1 hydroxyl group of the sugar substrate, and the histidine as the active site acid to protonate the C-5 ring oxygen.	3.27471e-97
NZ_CP045802.1|WP_028599044.1|5226886_5227804_-|ABC-transporter-permease	gnl|CDD|225088	COG2177, FtsX, Cell division protein [Cell division and chromosome partitioning].	1.22221e-68
NZ_CP045802.1|WP_028599054.1|5211944_5212814_+|SDR-family-oxidoreductase	gnl|CDD|235853	PRK06701, PRK06701, short chain dehydrogenase; Provisional.	0
NZ_CP045802.1|WP_052333258.1|5223114_5224611_-|S41-family-peptidase	gnl|CDD|223864	COG0793, Prc, Periplasmic protease [Cell envelope biogenesis, outer membrane].	2.19785e-109
NZ_CP045802.1|WP_028599047.1|5224734_5225145_-|DUF86-domain-containing-protein	gnl|CDD|366864	pfam01934, DUF86, Protein of unknown function DUF86. The function of members of this family is unknown.	1.92392e-27
NZ_CP045802.1|WP_153783988.1|5218245_5219505_-|IS256-family-transposase	gnl|CDD|307151	pfam00872, Transposase_mut, Transposase, Mutator family.	6.8439e-147
NZ_CP045802.1|WP_153784410.1|5220025_5221306_-|voltage-gated-chloride-channel-protein	gnl|CDD|239654	cd03682, ClC_sycA_like, ClC sycA-like chloride channel proteins. This ClC family presents in bacteria, where it facilitates acid resistance in acidic soil. Mutation of this gene (sycA) in Rhizobium tropici CIAT899 causes serious deficiencies in nodule development, nodulation competitiveness, and N2 fixation on Phaseolus vulgaris plants, due to its reduced ability for acid resistance. This family is part of the ClC chloride channel superfamiy. These proteins catalyse the selective flow of Cl- ions across cell membranes and Cl-/H+ exchange transport. These proteins share two characteristics that are apparently inherent to the entire ClC chloride channel superfamily: a unique double-barreled architecture and voltage-dependent gating mechanism. The gating is conferred by the permeating anion itself, acting as the gating charge.	5.42023e-156
NZ_CP045802.1|WP_101807662.1|5221696_5223004_-|PDZ-domain-containing-protein	gnl|CDD|238487	cd00987, PDZ_serine_protease, PDZ domain of trypsin-like serine proteases, such as DegP/HtrA, which are oligomeric proteins involved in heat-shock response, chaperone function, and apoptosis. May be responsible for substrate recognition and/or binding, as most PDZ domains bind C-terminal polypeptides, though binding to internal (non-C-terminal) polypeptides and even to lipids has been demonstrated. In this subfamily of protease-associated PDZ domains a C-terminal beta-strand forms the peptide-binding groove base, a circular permutation with respect to PDZ domains found in Eumetazoan signaling proteins.	1.7763e-08
NZ_CP045802.1|WP_084137297.1|5227793_5228486_-|cell-division-ATP-binding-protein-FtsE	gnl|CDD|225438	COG2884, FtsE, Predicted ATPase involved in cell division [Cell division and chromosome partitioning].	3.56826e-127
NZ_CP045802.1|WP_028599046.1|5225134_5225542_-|nucleotidyltransferase-domain-containing-protein	gnl|CDD|376187	pfam18765, Polbeta, Polymerase beta, Nucleotidyltransferase. A member of the nucleotidyltransferase fold found in polymorphic toxins (NTox45) and polyvalent proteins.	3.68385e-21
NZ_CP045802.1|WP_084137302.1|5211241_5211898_-|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.	3.29139e-09
NZ_CP045802.1|WP_153784808.1|5225680_5226811_-|peptidoglycan-DD-metalloendopeptidase-family-protein	gnl|CDD|366703	pfam01551, Peptidase_M23, Peptidase family M23. Members of this family are zinc metallopeptidases with a range of specificities. The peptidase family M23 is included in this family, these are Gly-Gly endopeptidases. Peptidase family M23 are also endopeptidases. This family also includes some bacterial lipoproteins for which no proteolytic activity has been demonstrated. This family also includes leukocyte cell-derived chemotaxin 2 (LECT2) proteins. LECT2 is a liver-specific protein which is thought to be linked to hepatocyte growth although the exact function of this protein is unknown.	9.51689e-46
NZ_CP045802.1|WP_153784407.1|5214253_5215171_-|D-alanyl-D-alanine-carboxypeptidase-family-protein	gnl|CDD|350624	cd14852, LD-carboxypeptidase, L,D-carboxypeptidase DacB and LdcB, and related proteins. This L,D-carboxypeptidase family includes LdcB LD-Carboxypeptidase from Streptococcus pneumoniae, Bacillus anthracis, and Bacillus subtilis, and L,D-carboxypeptidase DacB from Streptococcus pneumonia and Lactococcus lactis. These enzymes are active against cell-wall-derived tetrapeptides and synthetic tetrapeptides lacking the sugar moiety but are inactive against tetrapeptides terminating in L-alanine. L,D-carboxypeptidase DacB plays a key role in the remodeling of S. pneumoniae peptidoglycan during cell division. It adopts a zinc-dependent carboxypeptidase fold and acts as an L,D-carboxypeptidase towards the tetrapeptide L-Ala-D-iGln-L-Lys-D-Ala of the peptidoglycan stem. This family also includes vanY D-Ala-D-Ala carboxypeptidase which is vancomycin-inducible and penicillin-resistant. VanY hydrolyzes depsipeptide- and D-alanyl-D-alanine-containing peptidoglycan precursors; it is insensitive to beta-lactams. All these enzymes belong to the MEROPS family M15 subfamily B.	3.34492e-83

Protein sequences

>NZ_CP045802.1|WP_153784409.1|5216354_5217656_+|peptidylprolyl-isomerase
MAENKKDPLDANGNDHLTPEDTATREGADFAGDSGSERREETIQAEEEVEERRTDDALRRAEYDAEVHTADPERAFGSLPVAPVAGAADLPLDNDGVHGDGDGGRPKRSGAATGWMIASLVLAVGLIIALVSLFSNRGGEAVATVNGEKITKDELYDMLAPTYGKSALDQLVTMKLVDQEADNKSVAVTEEEENAELEDIKKNFTSEAEFENALAQSGMSLDDLKKQMLMQVQMRKLLADQVKVSDEDIKKNYEENKESFATPEQVQASHILVATKEEADAIEKQLKNGGDFAAIAKEKSTDTGSAANGGDLGFFGKGSMVPEFEEAAFGMKVGEISAPIKSDYGYHIIKLVDRKEATTPTLEDKKEEIRKTLENQQLSTLSQTLITDLRAKATITNTLDPSQNTNGSAEKNGSSENAPAENAPAENAASNSK
>NZ_CP045802.1|WP_153784408.1|5215390_5216236_+|alpha/beta-hydrolase
METKAPRKAPFELRLGDGGTIRGEVRFVPGGGRKPVVLIAHGFKGFKDWGFLPYAAERIAEAGFYAVTFNFSRNGVSGGEAFDELNKFALNTYSREQSDLERIVAALAGRELPHPEQADAKRIGICGHSRGGGNAIVFASEHPIVRAAVTWNGIARANLFDAEFEAAARRDGEAFVPNARTGQQMPIGKGFFEDLDRSGERFDIPARLASLRAPVLLIQGDADSSRLIEGFGRLKEAAPRQPSLLLEGASHTFGASHPFAGATPELNAALDASVRFLQEKM
>NZ_CP045802.1|WP_153784407.1|5214253_5215171_-|D-alanyl-D-alanine-carboxypeptidase-family-protein
MNSKRNRMPAASALLLAAALTLSACSGAAAPEPDASPGASATASPPASAGGGGSSASPSPSLTPSPSSSPTAKPSSSPSAKPSSKPSASPAGAKGGSSGGFYEAIEVTANASAAAALVNKQFRLPEGYAPKDLVYPDIPFTFSEKIDKRKLRKEAAEALEQLVAGAAKDGIKLAGVSGYRSESRQKTLYEGYVKKDGVAAADKYSARPGHSEHQTGLAIDMSGIDGKCAAESCFAGTPEAEWLAEHATDYGFIIRYPEGKEDITGYKYEPWHIRYVGVELAAKLAESGDTLEEHYGGAVPVSGGN
>NZ_CP045802.1|WP_101807664.1|5213073_5213982_-|NAD(P)/FAD-dependent-oxidoreductase
MVIDCAIIGGGPAGLAAALVLGRARRSALVVDDARPRNAVTAAGHGYPTRDGVPPGELRRLAREELAAYPGIRLRSGKVAAIEGRAGRFRVHLEGGGGFEARTVLLAAGLKEQLPDIPGLRELYGTSLFNCPYCDGWELRDASLVAISTGGNLFQQAKQLLVWSRDLLVCTHGRGQLSPQQQQALEARGARVARAPIAALEGSGGKLHAVRFADGSRIARSGGFVTPDAMLGTPLGAMLGCAHDAHGVLLVDGFGRTSVPGVYAAGDTAGMSPSQVVGAAASGNRAAFSIGGDLAEADFGPA
>NZ_CP045802.1|WP_028599054.1|5211944_5212814_+|SDR-family-oxidoreductase
MSSPTETVKTFPPQHQDKQPGIESEMNPLPVYAAPDYRGSGKLEGKKALITGGDSGIGRAAAIAFAKEGADVAIVYLSEDADAEQTKKEIEAAGRSCLLLAGDIGDEAFAKEAVSRTVEALGGLDVLVNNAAEQHPQPKFEDITAEQLEKTFRTNIFSMFHLTKAALPHLKPGSSIVNTASVTAYEGNPQLIDYSSTKGAIVSFTRALSNHLVERGIRVNGVAPGPIWTPLIPSTFDEQHVSEFGGDTPMKRAGQPHELAPAYVYLASSDSSYVSGQMIHINGGQVLNG
>NZ_CP045802.1|WP_084137302.1|5211241_5211898_-|GNAT-family-N-acetyltransferase
MPPGSTERSSSGPAERQGGNRMNTQAIEMIEPEAAAGFAAEIVTPDTAAEASELLVGIARWLRGNGSRQWSGLLDGEDSHGLDEAVRRGEAILFRDGMDGPGREKGRPAGLVLLLRQPGAWDRELWGEQGHEPYVYLHRLAVARAYAGSGLGRAILRWAREQAVHPGKKAIRLDCIAGNPKLEALYASAGYSRLGTSPNGFCLFEQALPEAQERRPSR
>NZ_CP045802.1|WP_043111322.1|5210246_5211107_+|aldose-epimerase
MYKEAYEMVELSEASTRSRVLLCPERGGIALECRLNGYELFYLDEATFLDPSANIRGGNPVLFPISGPVAGGEYEWEGKPYAMKQHGVARTEAWQVAETSEDGAASATLVLRSSERTRAAFPFDFELRFAYALKDGELTIRQQYRNLSDRAMPMYPGFHPYFATSAKDIPFATDATRYLDYNDGQVKPYEGRLDLGLMQESAALLDARRPEISFPLDSGITVTLAYSEAFKYVVLWSVPGKPFVCVEPWMALSGELDRREELVQVPPGGEIEAVLTLRASHAPGQG
>NZ_CP045802.1|WP_153784406.1|5208605_5210084_-|HD-domain-containing-protein
MRRPAVRMMSVALVSFLLPLGMFLALRESGGFDPRLHAPIIHFYIVSGVSFLALLLAAALGYAGMRLRNFGIAFLSLAYVSMTGLLMLHGLATPGFLMDHNSVQGVSSQLGILAAAGWIWLSSLPAARRMVLRLGNASRWLAPAYTLLLLAFLVFSLQGPHTMHDWALDLQGSRPALTGLVLALLAHAAWSYARNYRSARMPLQLGILYGCGLLAAGQVVMVSGEPWRLSWWLYHVLLLLSLVSVAWGLGRQLAGSRGSLSAALRALYRSTPQEWLQKCISPSVEDLIEATEQKDGYTAGHNYRVALYALKLAEKLDLAPEQLLAIGQGAIVHDVGKLYVPEAILNKPAALSPEERQVVELHPVRGYELCRNLGFMRQELAVVRSHHERWDGTGYPDRLEAEQIPLTARIAAVADVYDALTSQRAYRRAMTPEQALAFIGAESGRHFDPACVAAWLELAEEEPEFFARMTEEDQRPLLGRSRAVPGSVPPLA
>NZ_CP045802.1|WP_028599057.1|5208285_5208504_+|hypothetical-protein
MMKSITYKNRSVPVFYPPGQEEAVRLLPDKLKEYELNFDFRKRWKRIASVEMSRDVAIFQYNDGTKLYLEVG
>NZ_CP045802.1|WP_153784405.1|5206620_5208018_-|sensor-histidine-kinase
MAFLKVFFTNISLLVTIAYLFNLGYKLFFHRIRPAAQQAAAALVFVASGILTMLFGLQLSDEVRFDLRQVPLLLAVLAFRSPWAVGLIGAGIGAGRLLFGIAPAAWAGVGNMLILGIAGALANVWFRKRRLSYPVRATITILGINLLNGINISLFGVIPFEVYWSRFFPLTFPLSVLLSGFFVYMIRDFSKEQERMKELGVKNDTLRLQTEELQAAKHELEEQAVQLKLASKYKSEFLANMSHELKTPLNSILLLSELIGDNEDERRTVEERRHGAMIHAAGRELLQQIEDILDLSRVEAGKLSIQIEPLSTLELMQSLQLQFEPQARRKGLRFDVEVDPEAPELLLTDPLRIRQILRNLLANAIKFTDAGGVALAVRAEPAADRTPWLRFDVVDSGIGIEPDKHELIFEAFRQADGAVTRTYGGTGLGLSISLQLAELLGGRLELESRAGGGSRFSLVLPVRMN
>NZ_CP045802.1|WP_153783988.1|5218245_5219505_-|IS256-family-transposase
MTQYQITVDQDILHQLFIGTDRDAGVARLLETVLNQVLTAQATDQLAAQTYERTSERKGYRNGSYERDVITRAGSVTLRVPRFRDGSFSTELFARYQRSEQALVLSLMEMVINGVSTRKVTKITEELCGTEFSKSTVSHLCKQLDPAVHDWNNRSLADHAFPFITIDAIYVKVREEGRICSRGVLVGYGVNEQGRREILGLRVDDTESEESWGAYFRWLKERGLHGVELVTSDYHGGLVKAIEKEFQGVSWQRCQTHFIKNVLNAAPKALQSEIKSRVRSIFDAPDMKTARSYLEQTLEAYAETAPKAMKILEDGFEDAVAVLAFPEAYRVRLRTSNGMERLNGDIRRRETVIRIFPNRASVLRLIGAMLMEENEYWMTKKPYMDMTDFKAWKKQKATQGAGSEEQETSTTMTEATDSL
>NZ_CP045802.1|WP_153784410.1|5220025_5221306_-|voltage-gated-chloride-channel-protein
MSEATGLKKRLAEAGKGKSAGGMVAFLLKWLALGSLVGALAGTASALFLWSLELATETRLEHSWLLFLLPAAGFFVSWIYRQYGGTAIRGSNLILESIHEGRERIPLRMAPLVLGGTVLTHLTGGSAGREGTAVQMGGSLAWLAGTLVRSGAADRRILLLCGMAGGFGSVFGTPLAGAVFGVEVLAIGMLRHGALYPCLVAALVGDAVTRAWGIGHAAYRIGEVPAESFGTLAAVAIAAVAFGLAARLFIAAVHGVRRLATRLVAPAPGRAAACGAVIVLLALLVGGGDYLGLSLPLLQDSFAPAGTVEPFAWLWKLVFTALTLGAGFQGGEVTPLFVIGSTLGHALAPLLQLPAPLLAGLGLVGVFSAAANTPLACFVLGLELFGADAAAYLLVASVIAYLCSGSASIYSSQRRTIRKDGREPVG
>NZ_CP045802.1|WP_153784411.1|5221304_5221700_+|hypothetical-protein
MPFPSFLIVLAKAKRPVPGRSACAGACTCTYAYAGACTCTFTYAGACTYACTCACTFTCTCTCTYAYAGACTFTCTYAYAGACTCTCAYTFTCTCHRLTARLRLRIRPRPWLTGPCACSCVHVRVSDLVRA
>NZ_CP045802.1|WP_101807662.1|5221696_5223004_-|PDZ-domain-containing-protein
MELTLELLRQYGSAALGLLAQPYYYLALIVMGFLYRRLAVTERSHFHVRLHAWPLLLLRAAGWGLLAGAGVSIAAAFIGAALTPDAVLWLWGTAAALALLRVRFLCFAYSAGVLGVLQAASGLLSLEESGGTAGRLGTSLAALDMPGLLLLVALLHVAEALLVKRDGQRLASPLYLEGKRGKLIGGYSLQGLWPVPLLLLVPASGGAEGAAAALPWTPLLGGEGWSAGWTVLALPAVIGFTDLALSELPKQAARLASRRLLIYSLILGALALAASYARPLVLVASLAALGLHEALTRLAERRERQRPPRFVHDERGLCILGVLPGTPAQEMGLEAGEVLRKVNGRGVRTKEELHAALHENSAFCRLEVLNLDGQVKFVQRARFAGEHHQLGVLLAPDEDAAYSAVPGRGSVLALLLRRGHKVRRRASGEPPSMEA
>NZ_CP045802.1|WP_052333258.1|5223114_5224611_-|S41-family-peptidase
MNRNENAAAGPRRLKAVLSASLAAALLLGGAWPAGEAGAKPASAEAARPAQAGERQDASAGLTKEEAQRLSAVMELIQRQYYEPVDRDKLISGALSGMVQALGDPYSTYMDAGAAKQFSETVEGAFGGVGAEVTSESGKVVIVSPIKGSPAEKAGLQAKDVILSVNGVGLSGLPISEAVAKLRGPKGSAAELVILRAGRANPFAVKLMRAEIDIETVEGKRLADGIGLIEIRQFSLNTADRFAAELAKLEKRELKGLVIDVRNNPGGILPVVERIAQPFVPKGKPILQIAQRGAKPEQVLSEGGGKPYPVAVLMNKGSASASEILAGALQESAGAVLVGETSFGKGTVQVSYDRQLEGGLVKMTIAKWLTPSGGWIHKRGIKPDVAVRPPALYAATRLSKTATIPADAISDDAKSLQVMLKGLGYDPGRLDGYYSSGTAEAVRGFQRASGLRASGQADPATQRKLEEAVQAWVSGDEHDTQLEAAVQALREGKGAPRH
>NZ_CP045802.1|WP_028599047.1|5224734_5225145_-|DUF86-domain-containing-protein
MKHDVILNKAANIERCLRRIGEVYQGRPEHLNDFTKQDSIVLNLQRACEASIDLAMAVVASGKLGVPQTSRDAFELLEQSGRLDSELADKMKAMVGFRNIAVHDYQKLNPDILRSILDLHLGDFTDFARAMLASDG
>NZ_CP045802.1|WP_028599046.1|5225134_5225542_-|nucleotidyltransferase-domain-containing-protein
MDARLDLDIAVDEIEKAVSPDLLLLFGSAAAGRMRADSDIDLAYYGGKPLSAYERFLLAQKLAGRLGREVDLVDLKEASTVMQMQILSEGHTLRCKDEDLDLRLRTQVYKMYAKLNEERSPVLRSIRERGSIYEA
>NZ_CP045802.1|WP_153784808.1|5225680_5226811_-|peptidoglycan-DD-metalloendopeptidase-family-protein
MPQAAGALSQSEKINRELKQVREQMQAAAQGRKQADAQSKTVLTQKFYTAESLKAVMTEIDIVGSRMSAVQSQVSSTTQALEQTARELDEAEQRIARQDERLQSRMRVTYMNGRVSYLDVLLNATSFSDFLGRLDSLHTIMVQDKETLLDRKQDKQLVVAKKAEVEQKLAEVKSLYAKVAEYQQVLASKEAQKTQLISSYNTKLDELGDISEEQEKLLLELAAKESALIKKKNSLKTTYSGGQLGAPVKASYRLSSPFGYRIHPISGTRKLHAGVDMAAPAGTNIYAAEGGIVLVAQWWSGYGNCIVIDHGGGLWTIYGHIRDGGILVEKGQTVKRGEHIGEVGSTGNSTGNHLHFEVRKNGEPVNPLPYLKGKAN
>NZ_CP045802.1|WP_028599044.1|5226886_5227804_-|ABC-transporter-permease
MKLRTLARHLREGVRGIFRNGWMSFASISSIFISLFILGVFVLLALNVSKLADQLESQVEIRAFLQLDATAESAAALETKLRAIPEVKSVEYRTPEQNLQEMSEMLGADGKQLLEDYQGEDNPLPASFTIEVYDPQTIAAAASQVQAVSAAQDPPAFQQIKYGQGTVETLFKITGAVRNIGLIIVAGLAVTAMFLIATTIKTTIIARQREIGIMKLVGATNAFIRWPFFVEGALIGFLSSALTAAVVVLGYGELIRQSEFDLGLMSIRLVSMEEAAGIIVPVTIGIGTLLGVWGSVLSVRRYLKV
>NZ_CP045802.1|WP_084137297.1|5227793_5228486_-|cell-division-ATP-binding-protein-FtsE
MPVIEMMDIWKTYPNGAHALKGISVVIDRNEFVYIVGPSGAGKSTFMKLIYREEFPTKGQLFVNGFNIGKLKPRKIPYVRRNIGVIFQDYRLLPKLTAYENVAFAMEVIEAPRKLMKKRTMEVLELVGLGGKHAHLPAQLSGGEQQRVAIARAIVNNPSVIVADEPTGNLDPETSWGIMNLLEEINFRGTTIVMATHNREIVNTLRKRVIAIENGLIARDQARGEYGYEA

Crispr_ID: NZ_CP045802_24

• CRISPR_ID: NZ_CP045802_24
• CRISPR_location: 5331205-5332165
• CRISPR_type: Orphan
• Repeat_type: NA:I-C
• Spacer_info: 14 spacers

Consensus repeat of NZ_CP045802_24

Consensus_repeat	Method
GTTTCAATCCACGCTCCCCAGCGGGGAGCGACN	CRT
GTTTCAATCCACGCTCCCC-AGCGGGGAGCGAC	PILER-CR
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	CRISPRCasFinder

spacers of NZ_CP045802_24

>24.1|5331237|34|NZ_CP045802|CRT
ACGGCGGAGCAGATGGCAGAGACGCGCGAATCGC
>24.2|5331303|33|NZ_CP045802|CRT
CAACACCGTCCTGACGCGATTGCTCACGCACCC
>24.3|5331368|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
GCGCAAGCAGTTCGAGGCGACGAAAAACACTATG
>24.4|5331434|36|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
TGATTGGACTCGATGGACGAAATCGCAGCAGCATCT
>24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
TCAGCGTATCGCCGATCTCGCCGCCTTCGCGGAG
>24.6|5331568|33|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
CGGGGCAACTGTATGCGGCTTCCCCACTTATCG
>24.7|5331633|36|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
GGGCATCGGGGCGATCATGGGCGGCATCAGCGGGGC
>24.8|5331701|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
GCGGCTCCCGGCAGCCGGCCGGCCTACCAACCGCC
>24.9|5331768|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
GTCAAGCAATGCGTCTGCTATTCGCTCATGTACG
>24.10|5331834|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
AATCGAACACCTCGTCGAGAGGCTATATCGTGTG
>24.11|5331900|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
TAATCAAAATGGCGACGTCCGACCGGCTCCGCTT
>24.12|5331966|33|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
TTTTTCACGACTCGAAGATATGAAATCGGAGTG
>24.13|5332031|37|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
GCGGTACAATCACCAAAAGGTTGATTGAGCTAGGCGA
>24.14|5332100|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder
CTCGCCGTTCTTCGTTGAGGGCGGCTTGCCTGGC

CRISPR arrays and Neighbor proteins around NZ_CP045802_24

CRISPR arrays

The CRISPR arrays of NZ_CP045802_24

>merge|NZ_CP045802|24|5331205-5332165|CRT,PILER-CR,CRISPRCasFinder
GCTTCCAATTACGCTCCATGCCGGGGAGGGACACGGCGGAGCAGATGGCAGAGACGCGCGAATCGCGTTTCAATTCATGCTCCCAGCGGGGAGTGACCCAACACCGTCCTGACGCGATTGCTCACGCACCCGTTTCAATCCACGCTCCCCAGCGGGGAGCGACGCGCAAGCAGTTCGAGGCGACGAAAAACACTATGGTTTCAATCCACGCTCCCCAGCGGGGAGCGACTGATTGGACTCGATGGACGAAATCGCAGCAGCATCTGTTTCAATCCACGCTCCCCAGCGGGGAGCGACTCAGCGTATCGCCGATCTCGCCGCCTTCGCGGAGGTTTCAATCCACGCTCCCCAGCGGGGAGCGACCGGGGCAACTGTATGCGGCTTCCCCACTTATCGGTTTCAATCCACGCTCCCCAGCGGGGAGCGACGGGCATCGGGGCGATCATGGGCGGCATCAGCGGGGCGTTTCAATCCACGCTCCCCAGCGGGGAGCGACGCGGCTCCCGGCAGCCGGCCGGCCTACCAACCGCCGTTTCAATCCACGCTCCCCAGCGGGGAGCGACGTCAAGCAATGCGTCTGCTATTCGCTCATGTACGGTTTCAATCCACGCTCCCCAGCGGGGAGCGACAATCGAACACCTCGTCGAGAGGCTATATCGTGTGGTTTCAATCCACGCTCCCCAGCGGGGAGCGACTAATCAAAATGGCGACGTCCGACCGGCTCCGCTTGTTTCAATCCACGTTCCCCAGCGGGGAGCGACTTTTTCACGACTCGAAGATATGAAATCGGAGTGGTTTCAATCCACGTTCCCCAGCGGGGAGCGACGCGGTACAATCACCAAAAGGTTGATTGAGCTAGGCGAGTTTCAATCCACGTTCCCCAGCGGGGAGCGACCTCGCCGTTCTTCGTTGAGGGCGGCTTGCCTGGCGTTTCAATCCACGTTCCCCAGCGGGGAGCGAC

>NZ_CP045802|24|7|5331205-5332165|CRT
GCTTCCAATTACGCTCCATGCCGGGGAGGGAC	ACGGCGGAGCAGATGGCAGAGACGCGCGAATCGC
GTTTCAATTCATGCTCCCAGCGGGGAGTGACC	CAACACCGTCCTGACGCGATTGCTCACGCACCC
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	GCGCAAGCAGTTCGAGGCGACGAAAAACACTATG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	TGATTGGACTCGATGGACGAAATCGCAGCAGCATCT
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	TCAGCGTATCGCCGATCTCGCCGCCTTCGCGGAG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	CGGGGCAACTGTATGCGGCTTCCCCACTTATCG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	GGGCATCGGGGCGATCATGGGCGGCATCAGCGGGGC
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	GCGGCTCCCGGCAGCCGGCCGGCCTACCAACCGCC
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	GTCAAGCAATGCGTCTGCTATTCGCTCATGTACG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	AATCGAACACCTCGTCGAGAGGCTATATCGTGTG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	TAATCAAAATGGCGACGTCCGACCGGCTCCGCTT
GTTTCAATCCACGTTCCCCAGCGGGGAGCGAC	TTTTTCACGACTCGAAGATATGAAATCGGAGTG
GTTTCAATCCACGTTCCCCAGCGGGGAGCGAC	GCGGTACAATCACCAAAAGGTTGATTGAGCTAGGCGA
GTTTCAATCCACGTTCCCCAGCGGGGAGCGAC	CTCGCCGTTCTTCGTTGAGGGCGGCTTGCCTGGC
GTTTCAATCCACGTTCCCCAGCGGGGAGCGAC

>NZ_CP045802|24|4|5331336-5332165|PILER-CR
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	GCGCAAGCAGTTCGAGGCGACGAAAAACACTATG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	TGATTGGACTCGATGGACGAAATCGCAGCAGCATCT
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	TCAGCGTATCGCCGATCTCGCCGCCTTCGCGGAG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	CGGGGCAACTGTATGCGGCTTCCCCACTTATCG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	GGGCATCGGGGCGATCATGGGCGGCATCAGCGGGGC
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	GCGGCTCCCGGCAGCCGGCCGGCCTACCAACCGCC
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	GTCAAGCAATGCGTCTGCTATTCGCTCATGTACG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	AATCGAACACCTCGTCGAGAGGCTATATCGTGTG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	TAATCAAAATGGCGACGTCCGACCGGCTCCGCTT
GTTTCAATCCACGTTCCCCAGCGGGGAGCGAC	TTTTTCACGACTCGAAGATATGAAATCGGAGTG
GTTTCAATCCACGTTCCCCAGCGGGGAGCGAC	GCGGTACAATCACCAAAAGGTTGATTGAGCTAGGCGA
GTTTCAATCCACGTTCCCCAGCGGGGAGCGAC	CTCGCCGTTCTTCGTTGAGGGCGGCTTGCCTGGC
GTTTCAATCCACGTTCCCCAGCGGGGAGCGAC

>NZ_CP045802|24|19|5331336-5332165|CRISPRCasFinder
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	GCGCAAGCAGTTCGAGGCGACGAAAAACACTATG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	TGATTGGACTCGATGGACGAAATCGCAGCAGCATCT
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	TCAGCGTATCGCCGATCTCGCCGCCTTCGCGGAG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	CGGGGCAACTGTATGCGGCTTCCCCACTTATCG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	GGGCATCGGGGCGATCATGGGCGGCATCAGCGGGGC
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	GCGGCTCCCGGCAGCCGGCCGGCCTACCAACCGCC
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	GTCAAGCAATGCGTCTGCTATTCGCTCATGTACG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	AATCGAACACCTCGTCGAGAGGCTATATCGTGTG
GTTTCAATCCACGCTCCCCAGCGGGGAGCGAC	TAATCAAAATGGCGACGTCCGACCGGCTCCGCTT
GTTTCAATCCACGTTCCCCAGCGGGGAGCGAC	TTTTTCACGACTCGAAGATATGAAATCGGAGTG
GTTTCAATCCACGTTCCCCAGCGGGGAGCGAC	GCGGTACAATCACCAAAAGGTTGATTGAGCTAGGCGA
GTTTCAATCCACGTTCCCCAGCGGGGAGCGAC	CTCGCCGTTCTTCGTTGAGGGCGGCTTGCCTGGC
GTTTCAATCCACGTTCCCCAGCGGGGAGCGAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_084137279.1|5324049_5324379_-|DNA-directed-RNA-polymerase-subunit-beta	unknown	unknown	gnl|CDD|378713
NZ_CP045802.1|WP_021880270.1|5327571_5327856_-|sporulation-transcriptional-regulator-SpoIIID	unknown	unknown	gnl|CDD|378813
NZ_CP045802.1|WP_028598974.1|5342501_5342972_-|DNA-starvation/stationary-phase-protection-protein	unknown	unknown	gnl|CDD|153102
NZ_CP045802.1|WP_028598985.1|5319085_5320795_-|phospho-sugar-mutase	unknown	unknown	gnl|CDD|100092
NZ_CP045802.1|WP_043111317.1|5321686_5323852_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028598975.1|5340064_5340322_-|DUF1146-domain-containing-protein	unknown	unknown	gnl|CDD|377678
NZ_CP045802.1|WP_101807702.1|5334707_5335865_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|182528
NZ_CP045802.1|WP_028598981.1|5326475_5327480_-|MreB/Mrl-family-cell-shape-determining-protein	unknown	unknown	gnl|CDD|237563
NZ_CP045802.1|WP_028598984.1|5320895_5321327_-|3-hydroxyacyl-ACP-dehydratase-FabZ	unknown	unknown	gnl|CDD|234568
NZ_CP045802.1|WP_052333247.1|5340528_5342271_-|S8-family-serine-peptidase	unknown	unknown	gnl|CDD|173803
NZ_CP045802.1|WP_084137275.1|5335839_5336649_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213222
NZ_CP045802.1|WP_084137314.1|5329039_5329894_-|stage-II-sporulation-protein-D	unknown	unknown	gnl|CDD|274332
NZ_CP045802.1|WP_153784453.1|5332417_5334001_-|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|274368
NZ_CP045802.1|WP_153784454.1|5336648_5338112_-|efflux-RND-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl|CDD|273776
NZ_CP045802.1|WP_028598979.1|5333997_5334681_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_CP045802.1|WP_028598983.1|5324434_5325286_-|flagellar-hook-basal-body-protein	unknown	unknown	gnl|CDD|227125
NZ_CP045802.1|WP_028598976.1|5338282_5339704_-|UDP-N-acetylglucosamine-1-carboxyvinyltransferase	unknown	unknown	gnl|CDD|236486
NZ_CP045802.1|WP_101807628.1|5325300_5326161_-|flagellar-hook-basal-body-protein	unknown	unknown	gnl|CDD|227125
NZ_CP045802.1|WP_084137277.1|5328071_5328920_-|M23-family-metallopeptidase	unknown	unknown	gnl|CDD|366703
NZ_CP045802.1|WP_043111315.1|5343193_5343991_+|hypothetical-protein	unknown	unknown	gnl|CDD|373047

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_084137279.1|5324049_5324379_-|DNA-directed-RNA-polymerase-subunit-beta	gnl|CDD|378713	pfam11772, EpuA, DNA-directed RNA polymerase subunit beta. This short 60-residue long bacterial family is the beta subunit of the DNA-directed RNA polymerase, likely to be EC:2.7.7.6. It is membrane-bound and is referred to by the name EpuA.	2.37289e-10
NZ_CP045802.1|WP_021880270.1|5327571_5327856_-|sporulation-transcriptional-regulator-SpoIIID	gnl|CDD|378813	pfam12116, SpoIIID, Stage III sporulation protein D. This stage III sporulation protein is a small DNA-binding family that is essential for gene expression of the mother-cell compartment during sporulation. The domain is found in bacteria and viruses, and is about 40 amino acids in length. It has a conserved RGG sequence motif.	1.25721e-36
NZ_CP045802.1|WP_028598974.1|5342501_5342972_-|DNA-starvation/stationary-phase-protection-protein	gnl|CDD|153102	cd01043, DPS, DPS protein, ferritin-like diiron-binding domain. DPS (DNA Protecting protein under Starved conditions) domain is a member of a broad superfamily of ferritin-like diiron-carboxylate proteins. Some DPS proteins nonspecifically bind DNA, protecting it from cleavage caused by reactive oxygen species such as the hydroxyl radicals produced during oxidation of Fe(II) by hydrogen peroxide. These proteins assemble into dodecameric structures, some form DPS-DNA co-crystalline complexes, and possess iron and H2O2 detoxification capabilities. Expression of DPS is induced by oxidative or nutritional stress, including metal ion starvation. Members of the DPS family are homopolymers formed by 12 four-helix bundle subunits that assemble with 23 symmetry into a hollow shell. The DPS ferroxidase site is unusual in that it is not located in a four-helix bundle as in ferritin, but is shared by 2-fold symmetry-related subunits providing the iron ligands. Many DPS sequences (e.g., E. coli) display an N-terminal extension of variable length that contains two or three positively charged lysine residues that extends into the solvent and is thought to play an important role in the stabilization of the complex with DNA. DPS Listeria Flp, Bacillus anthracis Dlp-1 and Dlp-2, and Helicobacter pylori HP-NAP which lack the N-terminal extension, do not bind DNA. DPS proteins from Helicobacter pylori, Treponema pallidum, and Borrelia burgdorferi are highly immunogenic.	7.44913e-58
NZ_CP045802.1|WP_028598985.1|5319085_5320795_-|phospho-sugar-mutase	gnl|CDD|100092	cd05799, PGM2, This CD includes PGM2 (phosphoglucomutase 2) and PGM2L1 (phosphoglucomutase 2-like 1). The mammalian PGM2 is thought to be a phosphopentomutase that catalyzes the conversion of the nucleoside breakdown products, ribose-1-phosphate and deoxyribose-1-phosphate to the corresponding 5-phosphopentoses. PGM2L1 is thought to catalyze the 1,3-bisphosphoglycerate-dependent synthesis of glucose 1,6-bisphosphate and other aldose-bisphosphates that serve as cofactors for several sugar phosphomutases and possibly also as regulators of glycolytic enzymes. PGM2 and PGM2L1 belong 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 bifunctional phosphomannomutase/phosphoglucomutase (PMM/PGM). 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_CP045802.1|WP_028598975.1|5340064_5340322_-|DUF1146-domain-containing-protein	gnl|CDD|377678	pfam06612, DUF1146, Protein of unknown function (DUF1146). This family consists of several hypothetical bacterial proteins of unknown function.	4.5797e-09
NZ_CP045802.1|WP_101807702.1|5334707_5335865_-|FtsX-like-permease-family-protein	gnl|CDD|182528	PRK10535, PRK10535, macrolide ABC transporter ATP-binding protein/permease MacB.	1.022e-66
NZ_CP045802.1|WP_028598981.1|5326475_5327480_-|MreB/Mrl-family-cell-shape-determining-protein	gnl|CDD|237563	PRK13928, PRK13928, rod shape-determining protein Mbl; Provisional.	0
NZ_CP045802.1|WP_028598984.1|5320895_5321327_-|3-hydroxyacyl-ACP-dehydratase-FabZ	gnl|CDD|234568	PRK00006, fabZ, 3-hydroxyacyl-ACP dehydratase FabZ.	4.88568e-84
NZ_CP045802.1|WP_052333247.1|5340528_5342271_-|S8-family-serine-peptidase	gnl|CDD|173803	cd07477, Peptidases_S8_Subtilisin_subset, Peptidase S8 family domain in Subtilisin proteins. This group is composed of many different subtilisins: Pro-TK-subtilisin, subtilisin Carlsberg, serine protease Pb92 subtilisin, and BPN subtilisins just to name a few. Pro-TK-subtilisin is a serine protease from the hyperthermophilic archaeon Thermococcus kodakaraensis and consists of a signal peptide, a propeptide, and a mature domain. TK-subtilisin is matured from pro-TK-subtilisin upon autoprocessing and degradation of the propeptide. Unlike other subtilisins though, the folding of the unprocessed form of pro-TK-subtilisin is induced by Ca2+ binding which is almost completed prior to autoprocessing. Ca2+ is required for activity unlike the bacterial subtilisins. The propeptide is not required for folding of the mature domain unlike the bacterial subtilases because of the stability produced from Ca2+ binding. Subtilisin Carlsberg is extremely similar in structure to subtilisin BPN'/Novo thought it has a 30% difference in amino acid sequence. The substrate binding regions are also similar and 2 possible Ca2+ binding sites have been identified recently. Subtilisin Carlsberg possesses the highest commercial importance as a proteolytic additive for detergents. Serine protease Pb92, the serine protease from the alkalophilic Bacillus strain PB92, also contains two calcium ions and the overall folding of the polypeptide chain closely resembles that of the subtilisins. Members of the peptidases S8 and S35 clan include endopeptidases, exopeptidases and also a tripeptidyl-peptidase. The S8 family has an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure and are not homologous to trypsin. The S53 family contains a catalytic triad Glu/Asp/Ser. The stability of these enzymes may be enhanced by calcium, some members have been shown to bind up to 4 ions via binding sites with different affinity. Some members of this clan contain disulfide bonds. These enzymes can be intra- and extracellular, some function at extreme temperatures and pH values.	6.69923e-57
NZ_CP045802.1|WP_084137275.1|5335839_5336649_-|ABC-transporter-ATP-binding-protein	gnl|CDD|213222	cd03255, ABC_MJ0796_LolCDE_FtsE, ATP-binding cassette domain of the transporters involved in export of lipoprotein and macrolide, and cell division protein. This family is comprised of MJ0796 ATP-binding cassette, macrolide-specific ABC-type efflux carrier (MacAB), and proteins involved in cell division (FtsE), and release of lipoproteins from the cytoplasmic membrane (LolCDE). They are clustered together phylogenetically. MacAB is an exporter that confers resistance to macrolides, while the LolCDE system is not a transporter at all. An FtsE null mutants showed filamentous growth and appeared viable on high salt medium only, indicating a role for FtsE in cell division and/or salt transport. The LolCDE complex catalyzes the release of lipoproteins from the cytoplasmic membrane prior to their targeting to the outer membrane.	2.78694e-116
NZ_CP045802.1|WP_084137314.1|5329039_5329894_-|stage-II-sporulation-protein-D	gnl|CDD|274332	TIGR02870, Stage_II_sporulation_protein_D, stage II sporulation protein D. Stage II sporulation protein D (SpoIID) is a protein of the endospore formation program in a number of lineages in the Firmicutes (low-GC Gram-positive bacteria). It is expressed in the mother cell compartment, under control of Sigma-E. SpoIID, along with SpoIIM and SpoIIP, is one of three major proteins involved in engulfment of the forespore by the mother cell. [Cellular processes, Sporulation and germination].	1.02385e-113
NZ_CP045802.1|WP_153784453.1|5332417_5334001_-|HAMP-domain-containing-protein	gnl|CDD|274368	TIGR02966, Phosphate_regulon_sensor_protein_PhoR, phosphate regulon sensor kinase PhoR. Members of this protein family are the regulatory histidine kinase PhoR associated with the phosphate ABC transporter in most Proteobacteria. Related proteins from Gram-positive organisms are not included in this model. The phoR gene usually is adjacent to the response regulator phoB gene (TIGR02154). [Signal transduction, Two-component systems].	1.93675e-59
NZ_CP045802.1|WP_153784454.1|5336648_5338112_-|efflux-RND-transporter-periplasmic-adaptor-subunit	gnl|CDD|273776	TIGR01730, COG0845:_Membrane-fusion_protein, RND family efflux transporter, MFP subunit. This model represents the MFP (membrane fusion protein) component of the RND family of transporters. RND refers to Resistance, Nodulation, and cell Division. It is, in part, a subfamily of pfam00529 (Pfam release 7.5) but hits substantial numbers of proteins missed by that model. The related HlyD secretion protein, for which pfam00529 is named, is outside the scope of this model. Attributed functions imply outward transport. These functions include nodulation, acriflavin resistance, heavy metal efflux, and multidrug resistance proteins. Most members of this family are found in Gram-negative bacteria. The proposed function of MFP proteins is to bring the inner and outer membranes together and enable transport to the outside of the outer membrane. Note, however, that a few members of this family are found in Gram-positive bacteria, where there is no outer membrane. [Transport and binding proteins, Unknown substrate].	8.3938e-34
NZ_CP045802.1|WP_028598979.1|5333997_5334681_-|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].	1.73603e-87
NZ_CP045802.1|WP_028598983.1|5324434_5325286_-|flagellar-hook-basal-body-protein	gnl|CDD|227125	COG4786, FlgG, Flagellar basal body rod protein [Cell motility and secretion].	1.25694e-64
NZ_CP045802.1|WP_028598976.1|5338282_5339704_-|UDP-N-acetylglucosamine-1-carboxyvinyltransferase	gnl|CDD|236486	PRK09369, PRK09369, UDP-N-acetylglucosamine 1-carboxyvinyltransferase; Validated.	0
NZ_CP045802.1|WP_101807628.1|5325300_5326161_-|flagellar-hook-basal-body-protein	gnl|CDD|227125	COG4786, FlgG, Flagellar basal body rod protein [Cell motility and secretion].	6.79534e-61
NZ_CP045802.1|WP_084137277.1|5328071_5328920_-|M23-family-metallopeptidase	gnl|CDD|366703	pfam01551, Peptidase_M23, Peptidase family M23. Members of this family are zinc metallopeptidases with a range of specificities. The peptidase family M23 is included in this family, these are Gly-Gly endopeptidases. Peptidase family M23 are also endopeptidases. This family also includes some bacterial lipoproteins for which no proteolytic activity has been demonstrated. This family also includes leukocyte cell-derived chemotaxin 2 (LECT2) proteins. LECT2 is a liver-specific protein which is thought to be linked to hepatocyte growth although the exact function of this protein is unknown.	1.21694e-23
NZ_CP045802.1|WP_043111315.1|5343193_5343991_+|hypothetical-protein	gnl|CDD|373047	pfam14398, ATPgrasp_YheCD, YheC/D like ATP-grasp. A member of the ATP-grasp fold predicted to be involved in the modification/biosynthesis of spore-wall and capsular proteins.	7.90335e-55

Protein sequences

>NZ_CP045802.1|WP_084137314.1|5329039_5329894_-|stage-II-sporulation-protein-D
MLVRVYLTEEKRVEKVPMELYVRGVLAGEMPIGFEPEALKAQAIAARTYIVKRLAAKDRSGVPGGAADVTDTTAHQVYVPLAELQKRWSGEERERNLAKLNAAVQQTRGQIVTYEGKPIEALFFSTSNGYTENSEDYWDASLPYLRSVASPWDKTISPEYKETTTMSLAAFWRKLGVSSKAGARSLRVLDTTDGRRIRKLAAGGQVLTGREVREKLGLPSTQFTWKVEGGDIEITTYGYGHGVGMSQWGADGMAKAGRSAYQILSHYYTGTEVVRTASLPRNPA
>NZ_CP045802.1|WP_084137277.1|5328071_5328920_-|M23-family-metallopeptidase
MNEQDQKNAKQDPPKNQLGGRKPASTYKKTLSRKWISPAIFVAAAAIIVTVMWLYQGDEQKTSTTETPESVQTEQGGQEQIQETVKPVPGETALWPVASVEDVLVKRGYFDRNASAAEQEASLVEQGNTYKGNTGIDLARADDQPFDVQAVLSGKVTLVQDQPTNGTVVEIAHGNGLVSVYQSLSGVTVKPGDEVKQATVIGKAGRNDLQKELGVHLHFALLKNDEHVDPSSLLPAAAPQLQTAAAQPEAGSSAAPDAAEQTDAGAADSAGAADGAQPDDAE
>NZ_CP045802.1|WP_021880270.1|5327571_5327856_-|sporulation-transcriptional-regulator-SpoIIID
MHDYIKERTIKIGRCIVETKHTVRTIAKEFGVSKSTVHKDLTERLPEINPDLADQVKHILEYHKSIRHLRGGEATKIKYKKSTKRREVLAAGKR
>NZ_CP045802.1|WP_028598981.1|5326475_5327480_-|MreB/Mrl-family-cell-shape-determining-protein
MLSKDIGIDLGTANVSIHVKGKGVVLDEPSVVAVETDTRRVLAVGDEAYRMVGRTPGNIVAIRPLRDGVIADFEITEMMLKAFIDRIGGRSWYSRPRILICAPTNITSVEQKAIREAAERCGAREVYMEEEPKAAAIGAGMDIYQPSGNMVVDIGGGTTDVAVLSMGDIVTSASIKVAGDTFDSDISRYIKAKYKLLIGERTSEEIKIRIGSVHSGARNDAIDIRGRDMVTGLPRTISIHSEEVREALSDSVAAIVAAAKTVLEQTPPELSADIIDRGVILTGGGALLDGLDLLMADELKVPVLVAEDPMHCVVKGTGYMLDHLDRMSRKKARI
>NZ_CP045802.1|WP_101807628.1|5325300_5326161_-|flagellar-hook-basal-body-protein
MIRGLYTAAAGMIAQQRVHDTATTNIANLNTTGYKASHALNRSFPEMLLSMSGKNDEPVRRIGRLSTGVLAEESIALQVQGDLNKTDKPSDFAILSEIQVPGVTFDASGKSVAEDGTVTYRPQAYFTVLNEQEQTRYTRGGEFHLTGEGALVTSDGSPVLGAGGQPIAFEPGTSLDSLKLDGSFRFVDATGAPTGQALLITQVDRVADLVREGDGKLRLDGEGGAAPAQPGAGIEVRQGYAERSNVDPTQTMLDLMGAMRAYEANQKVIQFYDKSLEKAANEIGRV
>NZ_CP045802.1|WP_028598983.1|5324434_5325286_-|flagellar-hook-basal-body-protein
MNNSIINATVSMSALQQRLDLLAENMANVNTAGYKRKEATFQDLLTNAKQQPEAFRREGRVGPLGYNQGWGARFIQMGPDMTQGSLKETGTSTDLALEGNALFVVASDDAGGRGYTRSGAFQLTVTGQGDTILATATGYPVLGQVPVQTANGVVLREGPIVVPEGVSLQISPEGVVDGVRADGSRTRLGQLSLVQPTRPESLVAAADNLFAVAAGTDAADVLTPVQAGEGGAVAVRQGFIEQSNVDLVEEMTELLSVQRAYQLSARALTSADTMAGLANNMRA
>NZ_CP045802.1|WP_084137279.1|5324049_5324379_-|DNA-directed-RNA-polymerase-subunit-beta
MMIMTNDTQASSMGGAPSPREGEKSSSASAGGAARPKEKQAAASSGKPRKKSRFTAWWFARKLIVLALFAGALVGGLYLGFVTVGGGSMSDAFDIATYKHIYDLIFSDS
>NZ_CP045802.1|WP_043111317.1|5321686_5323852_+|hypothetical-protein
MTRHATPRGRTLLSLLLAAVLALSLLAPAAHAEDAVTSVSLDAGSSLSLTYGEDPFALVLWASYSGSSAKKDVTSSAVWTTSLSSVVKVSGGVLTPVASGKATITGKFGGYSASVAVTVEYPYSKLQLQRGGENAPSKLEAAVGDKLQLDVLGVKNGLTTELTEDADWTSSSAAVATVKDGEIEILSAGTTTIKASYRGVSASLTLTAESPYKAIELSETSLVELETGGSPARLSATAQPKDGGASLDVTSKAVWSSSAPTVVKAEKDGVLTPVGPGTATISVSLHGVTATVQAVVRQPYEVLKLSPSAELHLLLSDSPVQLSASIPSASGSAEDVTALAAWTSSDLYAATADGGLVTPKAAGSSTIKAEYKGVSRSLKVTVYPTAVRIKAAEEKLSAIVEETRELPSITAAGLDDAEFSVTKLVKWTSSDSDIVEIKDGKWIARKSGSAVLKAELGDMSVELPFEVNAKPLALLSETKNLSLVIGKTVGLPKLTITYTTGEEEDVTAKAVWKASGSSLLVLEDSMRGLASAKTTLTASYLGKTVSFPVTIEEEIVKLTVDPSSLTLNPNRSKTVKVTGTYKSGSTVSLAAKMDWSTDASAVASVQRGTIKALKLGSAKLTGTYQGKSVTVSLSVKPKLKSLVLSEKSLKLAPGASAQLKLKAFYDNGTYEEVTAASLWSSSRESSAAVTQGGTVSAVAKGTATIKAVFDGKSVTARVTVK
>NZ_CP045802.1|WP_028598984.1|5320895_5321327_-|3-hydroxyacyl-ACP-dehydratase-FabZ
MLNINEIMDIIPHRQPFLLIDRILEVEEGRRAVGLKNVTMNEPFFAGHFPGFPVMPGVLIVEALAQVGAVAILKLEANRGKLAMFAGIDEFRFRGQVTPGDTLRLEVEITRLKGIVGKGKATASVDGKVVAEGGIMFALTDPS
>NZ_CP045802.1|WP_028598985.1|5319085_5320795_-|phospho-sugar-mutase
MSVTAIATERYHAWLSDPLIDEATKEELRGIAGDEKEITDRFYRDLEFGTGGLRGVMGAGTNRLNAYTVGKATQGLAQWLLAQTDSPSVVIAHDSRNNSPEFTLDAALVLAGNGIKTYLFPSLRPTPQLSFAVRDLGASGGIVITASHNPPEYNGYKAYGPEGCQLVPHEAEQAIAAIGRVGSFAEIKRIGREEAEAKGLLVWLGAADDRRFIEAVAAQSLNRDLLKRGAGSDLKVVFTPLHGTGNHPVREALAEIGLSNVSVVQEQEQPDGYFSTVKSPNPEEREAFTLAIRQAQEQDADLIIGTDPDADRVGAVVKNNRGEYVVLTGNQSGALLVNYVLSQLKERGQLPANGVVVKTIVTSEMGADIAKAHGADVIDTLTGFKYIGEKMTEFERTGSHAFLFGYEESYGYLTGMYARDKDAVVAAMLIAEAAAYYKHQGKTLYDVLLELYDEYGTYLEGLESRTLKGLDGVQKIGAIMDSFRSAPPAEAGGVKIAEVLDYSIGLDGLPKENVLKYLLEDGSWFTLRPSGTEPKIKVYFAVRGESQQAAGEALDALRSSVMERVDAMA
>NZ_CP045802.1|WP_153784453.1|5332417_5334001_-|HAMP-domain-containing-protein
MSAGGLKDAARRLGERAAAVARRLGVGGIFAKLLLISLSTLAVTFLVYNLLSSQLVGRDMLDRRQGVEGAELRRTITLLETAARDGWSDDSIRTALQLVVPPQMKSILIIDRGGRYMQIGQVPLPESDIRELIASAGIGRSPEARTEMVENDSGKYIVSSQYVPSLDRYVVSLSTGFQREFRRVQNLNALAIGIAIAVSVLVSWAFSRYMTRRIRRMSLGAEQFAKGRFETKIADRSADELGQLAGSLNRMAGELGALEQMRRDFLANVSHDLRSPLTSIHGYLEAILDGTVPRDKADRYLRITQDQTARLMKLVSDLLDMSKIEAGQFDVVPAEFDLADMIRLLLSRMESTFSHHSVRYEIAGLPGGERRERAEPEGAEAGMAGTAGAPRAAEPGEVLVVGDPHRLEQVMVNLLQNAMAFSPHGSTVHVTLECGPDRACVSVRDEGIGMSEEQARRIWERFYKSDEARGGRGGTGIGLSIVKHILDAHGSRIEVRSEPGQGSEFRFCLVRAGLAGSDEQYRESSEK
>NZ_CP045802.1|WP_028598979.1|5333997_5334681_-|response-regulator-transcription-factor
MKSPSILLIEDDPLITDLLELYLERYGFRFSVAHDGAAGLARFYDQIPDLVVLDVMMPGRDGWSVCEEIRSASKVPIIFLTGKGEGYDKLKGFSLGADDYLVKPFDPKELIARIRAVLKRTHPTLYKDSAEFPDLVVDATEYRVLVRGKDAGCAPKEVELLYCLASRPGKVFSREELLQAVWGMDYFGDSNTVDVHIKRIRDRIGEHPAWRIGTVRGVGYRFEAGAS
>NZ_CP045802.1|WP_101807702.1|5334707_5335865_-|FtsX-like-permease-family-protein
MAWSSILANKLRTALSMLGILIGVATVISLVAMGQGSANEVSAQLQGLGTNMLSVNVTGRGSSTTLTLPQAETLGDGIDGIDGLSPTVSGSAAARYGSVQTESSVTVEGVTPDYEDVQDFHPQEGRFIAPLDLEAYSKVALLGIDTSEELFGPGVSPVGETILLSGVKYKVVGLLEPKGTSLGASNDEKILVPITTAQRLFQSEGVRTVAVKAASEETMDAVTAALEAKLSAIFRGNTNSYRITNSEELKETATSVSKTMSTMMAGVAAISLLVGGIGIMNIMLVSVTERTREIGIRKALGARKRDVLLQFLVEAASISSLGGALGIAAAFGAAAIMERTGTATQIESDIVLYSFVFSALVGIVFGLFPANKAASLKPVDALRHD
>NZ_CP045802.1|WP_084137275.1|5335839_5336649_-|ABC-transporter-ATP-binding-protein
MGRGRRTAAAHGDVSLTATLPPSSERAPLISIRDVRKSYRMAGEEVPILKGVDLEVMAGDFLAIIGPSGSGKSTLMNVIGCLDTPTSGSYKLDGQEVGGLSENRLAEVRNRGIGFIFQSFHLLPRMTARENVELPLIYRGLSGKERREAAEAALAKVGLADRMDHRPNQLSGGQMQRVAIARALAGHPPILLADEPTGALDTKTGAEVLGLVQELNRQGHTIVLITHDLDVAAKAGRIAFMKDGLLTEEGGDAREAFARHPHGLEQHSR
>NZ_CP045802.1|WP_153784454.1|5336648_5338112_-|efflux-RND-transporter-periplasmic-adaptor-subunit
MRKWMVVLGVLILAGGGYAYYAYRSQDQAPAAAAATARTVQATQGSIETSVSGSGTVAAADPTVVRTGRQGTVEKVLVQEGDEVKAGQTLLTFEKKDNALSIRQKQLEQSKQELSLQQLKIQYWQEGDEDKQDELMLQIDSAKLSLEQLAADIADLQAEQNADGKVVAPAAGTVTSVAVEAGQEVNGSVEAVTLTDYSELTFTMSADELDVPKLKAGQPAEIVLNALPDETFEGEITEIARAGTSSNGVASYPVTIRMTRLDGVLAGMSGSVKIVTESADNAVLVPVDAVVTMAGKSYVRVPASGTDAAAGGAGAAAADGASGQGQGQWQGQRGERPAGSGQGQPGTGAAGQAGAAGQPAAAGQAGSAGQVGAAGQAEAAGEAGATAGQSGSNRANRMALGGQLQEVEVGLISEDYAQIVSGLSAGDSVLVPLPTGTVGGSTGQSTQQGGFGAGGGFGGGAAGFGGGMPGGMGGGGGFAGGMGGGRN
>NZ_CP045802.1|WP_028598976.1|5338282_5339704_-|UDP-N-acetylglucosamine-1-carboxyvinyltransferase
MSKIVVRGGRRLEGTVRVHGAKNAVLPILAASLLATEGESVICDVPLLDDVLTIRQVLETLGATAVIGEDCMTISAERLTSCEAPYEWVSKMRASFLVMGPLLARLGKVRISMPGGCAIGTRPIDQHLKGFEAMGAEITIGQGFVEASAPDRLKGAKIYLDVASVGATENIMMAAALAEGTTTLENAAKEPEIVDLANYLNAMGARVRGAGTGMIRIEGVEKLVGARHHVIPDRVEAGTFLIAAAITGGDVFVEGAISDHLGPVIAKLQEMGVQLTEEDTGIRVTAGRPLRGVDVKTLPHPGFPTDMQSQMMALLLVSEGTSVVTETVFENRFMHVDEFRKMNANIKVEGRSAIITGGVPLYGAKVTATDLRAGAALICAGLVADGETEVGGLHHVDRGYVDIAGKLAALGADIRRTEPVEPAQELLEPIVLPSLREPAETEEVQVAAAAASEEDSYKAEQEVAIEDVEATLA
>NZ_CP045802.1|WP_028598975.1|5340064_5340322_-|DUF1146-domain-containing-protein
MNSNQGIREAFTSLGLVGLFSILVTILSILLAWYLLQELKLDTWFKHPRGPRARVLIAVLAVILGHQFARFILDYWSWTNMLKLI
>NZ_CP045802.1|WP_052333247.1|5340528_5342271_-|S8-family-serine-peptidase
MNRWHILAATLRRKRLAAVASAVFLTSVLGAGPAHPNEPVRVLSARSASPAEAAATGPAGASPAAAAQKEQQAYLRQIGALEVQSARKQSSGLTVAIVDTGVDLQHPALKGRLLPGVNLLQPGKPPQDDNGHGTSVAGVVAALLPQAKLLPVKALDENGYAEERGLGEGIRKALDKGARIVVLSVGLYHSSPYMADIVNRAERTGVLLVAAAGNDMQRFGGKTTVKYPAAYPTVLAVGGVAADGAPERRSSRGSEIDVAGAWRVFTAQLGGGYRYEEGTSMAAPQAAAAAALLWSKYPALKPYEIRSFLRQTTKDTLPAGFDRATGYGLLRMDQSLGGKYKADPHEPNDTRALAAALPLGKQLSAELAGGGDRDWYVLDCPHDGSVKLRLQQLLSPDAAPAPLDVLLEQDGGTVEKKLAASNNVLVWRVKKGANRLRIQLQGAGMEKAAPYLLSSVFSMRPDDGEPNGSAEEATALPDRSQTVKATFHETGDSDWYKIQVQKEGRLRLQLEPGTMRMDPAFAYRRAGSPETAVDEAGEGAAEASASIRVSPGTYYVRVWDAAELPYAPPEGYYTLSIERS
>NZ_CP045802.1|WP_028598974.1|5342501_5342972_-|DNA-starvation/stationary-phase-protection-protein
MATSSASRAAKANVKTQEALNKQVATLGVLYMKLHSFHWNVTGPNFYTLHVKFEELYNAVTLMFDEAAERLIAIGGKPVSTMKGMLSQSAIKEATEKEDADAMVRAVIDDFATIASEMKEAAEAAEKEDDAATADILTGMVEQLDKHRWMLEKFLG
>NZ_CP045802.1|WP_043111315.1|5343193_5343991_+|hypothetical-protein
MPSVKKYVKRYKSRALWGKLRVSRMLKKDPATAGLVPAAKPFSLERLTQMASRYEMLYIKPNIGSLGMGVHRLRRTASGDYELASVLSRKQTTRSFRTIDAVYRHLKRRKSGKKLLIQRGIPLDQVEGRPYDLRAMVQRRPKGPWTCTAFTAKIASPSKIVTNVHQGAKLVMLSSLWEMQGLPASAARANTDLIERKALAVSRSLSRRYKGMHEMGIDFAIDRSKKLWVLEVNTNHPQFRPVKKLDRAAYNRMASFARSYGRYDD

Crispr_ID: NZ_CP045802_26

• CRISPR_ID: NZ_CP045802_26
• CRISPR_location: 5386405-5386476
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_26

Consensus_repeat	Method
GTCCGCCGCAGCGTCTCCGCCAG	CRISPRCasFinder

spacers of NZ_CP045802_26

>26.1|5386428|26|NZ_CP045802|CRISPRCasFinder
AGTTGTTGTTGAAAATGACCTCCACC

CRISPR arrays and Neighbor proteins around NZ_CP045802_26

CRISPR arrays

The CRISPR arrays of NZ_CP045802_26

>merge|NZ_CP045802|26|5386405-5386476|CRISPRCasFinder
GTTGTCCGCGGCGTCTCCCCCGGAGTTGTTGTTGAAAATGACCTCCACCGTCCGGCTCTGCGCCTCCAGCCG

>NZ_CP045802|26|21|5386405-5386476|CRISPRCasFinder
GTTGTCCGCGGCGTCTCCCCCGG	AGTTGTTGTTGAAAATGACCTCCACC
GTCCGGCTCTGCGCCTCCAGCCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_153784462.1|5387292_5387559_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028598938.1|5379931_5380810_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP045802.1|WP_153784469.1|5394775_5395684_+|glycosyltransferase-family-2-protein	unknown	unknown	gnl|CDD|133029
NZ_CP045802.1|WP_153784468.1|5393696_5394752_+|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|187566
NZ_CP045802.1|WP_101807611.1|5379091_5379928_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP045802.1|WP_153784465.1|5390395_5391823_-|undecaprenyl-phosphate-glucose-phosphotransferase	unknown	unknown	gnl|CDD|274396
NZ_CP045802.1|WP_153784467.1|5392921_5393656_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213187
NZ_CP045802.1|WP_052333269.1|5374000_5374780_-|aldo/keto-reductase	unknown	unknown	gnl|CDD|381383
NZ_CP045802.1|WP_028598941.1|5376852_5378067_-|N-acyl-D-glucosamine-2-epimerase	unknown	unknown	gnl|CDD|238153
NZ_CP045802.1|WP_153784471.1|5397687_5398809_-|glycosyltransferase	unknown	unknown	gnl|CDD|224137
NZ_CP045802.1|WP_153784810.1|5384656_5385682_-|LacI-family-transcriptional-regulator	unknown	unknown	gnl|CDD|380629
NZ_CP045802.1|WP_052333243.1|5382759_5384664_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_CP045802.1|WP_153784461.1|5378067_5379051_-|1,4-beta-xylanase	unknown	unknown	gnl|CDD|381624
NZ_CP045802.1|WP_028598945.1|5373432_5373858_-|Rrf2-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224870
NZ_CP045802.1|WP_028598937.1|5381255_5382767_-|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_CP045802.1|WP_028598942.1|5375405_5376728_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270452
NZ_CP045802.1|WP_153784466.1|5392095_5392911_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|224596
NZ_CP045802.1|WP_153784470.1|5395680_5397513_+|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|132997
NZ_CP045802.1|WP_153784463.1|5387809_5388562_+|DsbA-family-oxidoreductase	unknown	unknown	gnl|CDD|239322
NZ_CP045802.1|WP_153784464.1|5389410_5390406_-|glycosyltransferase	unknown	unknown	gnl|CDD|366154

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_028598938.1|5379931_5380810_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	3.25921e-72
NZ_CP045802.1|WP_153784469.1|5394775_5395684_+|glycosyltransferase-family-2-protein	gnl|CDD|133029	cd04186, GT_2_like_c, Subfamily of Glycosyltransferase Family GT2 of unknown function. GT-2 includes diverse families of glycosyltransferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	1.1981e-31
NZ_CP045802.1|WP_153784468.1|5393696_5394752_+|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|187566	cd05256, UDP_AE_SDR_e, UDP-N-acetylglucosamine 4-epimerase, extended (e) SDRs. This subgroup contains UDP-N-acetylglucosamine 4-epimerase of Pseudomonas aeruginosa, WbpP, an extended SDR, that catalyzes the NAD+ dependent conversion of UDP-GlcNAc and UDPGalNA to UDP-Glc and UDP-Gal. This subgroup has the characteristic active site tetrad and NAD-binding motif of the extended SDRs. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	1.52306e-59
NZ_CP045802.1|WP_101807611.1|5379091_5379928_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	8.79331e-57
NZ_CP045802.1|WP_153784465.1|5390395_5391823_-|undecaprenyl-phosphate-glucose-phosphotransferase	gnl|CDD|274396	TIGR03023, Sugar_transferase., Undecaprenyl-phosphate glucose phosphotransferase. This family of proteins encompasses the E. coli WcaJ protein involved in colanic acid biosynthesis, the Methylobacillus EpsB protein involved in methanolan biosynthesis, as well as the GumD protein involved in the biosynthesis of xanthan. All of these are closely related to the well-characterized WbaP (formerly RfbP) protein, which is the first enzyme in O-antigen biosynthesis in Salmonella typhimurium. The enzyme transfers galactose from UDP-galactose (NOTE: not glucose) to a polyprenyl carrier (utilizing the highly conserved C-terminal sugar transferase domain, pfam02397) a reaction which takes place at the cytoplasmic face of the inner membrane. The N-terminal hydrophobic domain is then believed to facilitate the "flippase" function of transferring the liposaccharide unit from the cytoplasmic face to the periplasmic face of the inner membrane. Most of these genes are found within large operons dedicated to the production of complex exopolysaccharides such as the enterobacterial O-antigen. Colanic acid biosynthesis utilizes a glucose-undecaprenyl carrier, knockout of EpsB abolishes incorporation of UDP-glucose into the lipid phase, and the C-terminal portion of GumD has been shown to be responsible for the glucosyl-1-transferase activity.	0
NZ_CP045802.1|WP_153784467.1|5392921_5393656_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|213187	cd03220, ABC_KpsT_Wzt, ATP-binding cassette component of polysaccharide transport system. The KpsT/Wzt ABC transporter subfamily is involved in extracellular polysaccharide export. Among the variety of membrane-linked or extracellular polysaccharides excreted by bacteria, only capsular polysaccharides, lipopolysaccharides, and teichoic acids have been shown to be exported by ABC transporters. A typical system is made of a conserved integral membrane and an ABC. In addition to these proteins, capsular polysaccharide exporter systems require two 'accessory' proteins to perform their function: a periplasmic (E.coli) or a lipid-anchored outer membrane protein called OMA (Neisseria meningitidis and Haemophilus influenza) and a cytoplasmic membrane protein MPA2.	6.98298e-100
NZ_CP045802.1|WP_052333269.1|5374000_5374780_-|aldo/keto-reductase	gnl|CDD|381383	cd19157, AKR_AKR5G1-3, AKR5G family of aldo-keto reductase (AKR). Bacillus subtilis glyoxal reductase (GR), uncharacterized oxidoreductase YtbE, and Bacillus aryabhattai aldo-keto reductase are founding members of aldo-keto reductase family 5 member G1-3 (AKR5G1-3), respectively. GR (YvgN, EC 1.1.1.283), also called methylglyoxal reductase, reduces glyoxal and methylglyoxal (2-oxopropanal). It is not involved in vitamin B6 biosynthesis.	3.26646e-171
NZ_CP045802.1|WP_028598941.1|5376852_5378067_-|N-acyl-D-glucosamine-2-epimerase	gnl|CDD|238153	cd00249, AGE, AGE domain; N-acyl-D-glucosamine 2-epimerase domain; Responsible for intermediate epimerization during biosynthesis of N-acetylneuraminic acid. Catalytic mechanism is believed to be via nucleotide elimination and readdition and is ATP modulated. AGE is structurally and mechanistically distinct from the other four types of epimerases. The AGE domain monomer is composed of an alpha(6)/alpha(6)-barrel, the structure of which is also found in glucoamylase and cellulase. The active form is a homodimer. The alignment also contains subtype III mannose 6-phosphate isomerases.	8.38586e-58
NZ_CP045802.1|WP_153784471.1|5397687_5398809_-|glycosyltransferase	gnl|CDD|224137	COG1216, COG1216, Predicted glycosyltransferases [General function prediction only].	6.31086e-37
NZ_CP045802.1|WP_153784810.1|5384656_5385682_-|LacI-family-transcriptional-regulator	gnl|CDD|380629	cd19974, PBP1_LacI-like, ligand-binding domain of uncharacterized DNA-binding regulatory proteins that are members of the LacI-GalR family of bacterial transcription repressors. This group includes the ligand-binding domain of uncharacterized DNA-binding regulatory proteins that are members of the LacI-GalR family of bacterial transcription repressors. The LacI-GalR family repressors 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.	7.77189e-96
NZ_CP045802.1|WP_052333243.1|5382759_5384664_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	8.4788e-53
NZ_CP045802.1|WP_153784461.1|5378067_5379051_-|1,4-beta-xylanase	gnl|CDD|381624	cd19606, GH113-like, Glycoside hydrolase family 113 beta-mannosidase and similar proteins. Family 113 glycoside hydrolases cleave (1->4)-beta-glycosidic linkages, such as endo-1,4-beta-mannanase. This family also includes TIM-barrel domains found in gene transfer agent proteins.	9.94199e-116
NZ_CP045802.1|WP_028598945.1|5373432_5373858_-|Rrf2-family-transcriptional-regulator	gnl|CDD|224870	COG1959, COG1959, Predicted transcriptional regulator [Transcription].	1.89174e-26
NZ_CP045802.1|WP_028598937.1|5381255_5382767_-|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	7.46714e-44
NZ_CP045802.1|WP_028598942.1|5375405_5376728_-|extracellular-solute-binding-protein	gnl|CDD|270452	cd14749, PBP2_XBP1_like, The periplasmic-binding component of ABC transport systems specific for xylo-oligosaccharides; possesses type 2 periplasmic binding fold. This group represents the periplasmic component of an ABC transport system XBP1 that shows preference for xylo-oligosaccharides in the order of xylotriose > xylobiose > xylotetraose. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.40094e-36
NZ_CP045802.1|WP_153784466.1|5392095_5392911_+|ABC-transporter-permease	gnl|CDD|224596	COG1682, TagG, ABC-type polysaccharide/polyol phosphate export systems, permease component [Carbohydrate transport and metabolism / Cell envelope biogenesis, outer membrane].	1.05751e-48
NZ_CP045802.1|WP_153784470.1|5395680_5397513_+|methyltransferase-domain-containing-protein	gnl|CDD|132997	cd00761, Glyco_tranf_GTA_type, Glycosyltransferase family A (GT-A) includes diverse families of glycosyl transferases with a common GT-A type structural fold. Glycosyltransferases (GTs) are enzymes that synthesize oligosaccharides, polysaccharides, and glycoconjugates by transferring the sugar moiety from an activated nucleotide-sugar donor to an acceptor molecule, which may be a growing oligosaccharide, a lipid, or a protein. Based on the stereochemistry of the donor and acceptor molecules, GTs are classified as either retaining or inverting enzymes. To date, all GT structures adopt one of two possible folds, termed GT-A fold and GT-B fold. This hierarchy includes diverse families of glycosyl transferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. The majority of the proteins in this superfamily are Glycosyltransferase family 2 (GT-2) proteins. But it also includes families GT-43, GT-6, GT-8, GT13 and GT-7; which are evolutionarily related to GT-2 and share structure similarities.	2.09906e-11
NZ_CP045802.1|WP_153784463.1|5387809_5388562_+|DsbA-family-oxidoreductase	gnl|CDD|239322	cd03024, DsbA_FrnE, DsbA family, FrnE subfamily; FrnE is a DsbA-like protein containing a CXXC motif. It is presumed to be a thiol oxidoreductase involved in polyketide biosynthesis, specifically in the production of the aromatic antibiotics frenolicin and nanaomycins.	7.55722e-51
NZ_CP045802.1|WP_153784464.1|5389410_5390406_-|glycosyltransferase	gnl|CDD|366154	pfam00535, Glycos_transf_2, Glycosyl transferase family 2. Diverse family, transferring sugar from UDP-glucose, UDP-N-acetyl- galactosamine, GDP-mannose or CDP-abequose, to a range of substrates including cellulose, dolichol phosphate and teichoic acids.	3.24713e-24

Protein sequences

>NZ_CP045802.1|WP_153784810.1|5384656_5385682_-|LacI-family-transcriptional-regulator
MGHPEPSGSGQASGATAIGGQPGVPGFPAGEAGRFSPASSRAASNPAATQAASDGLGSQVIILVPNVRFQTRLSYYWGRIIEGVQEELEERGIGSILITEQGTTRFSSLINPRGVMGLVGVGFISYPVLLEIRNLGIPTVLIDHEEPLVPTDVLSMNNFEWMRRVANYLIGLGHRRLQFVGNLTYSRSFYDRWFGFRAMMEEHGLSTDGQHDGLLTVRGHNRSEMTEALEPMLQELRREGRMPTAFACANDSIAICIMTILARMGVSVPEDVSVAGFDDIEDAALSSPTLTTVHVHKHGMGRRAVEALLRRVQQPASPVEKVLLTGELVIRASTGAARADG
>NZ_CP045802.1|WP_052333243.1|5382759_5384664_-|sensor-histidine-kinase
MARLWSALRQQLEPLLHRLETRLLLVYFLLVLLPIAVITYVSASHNFATIEQNTVTYASQVSDRMLNSLDDYIHDMKQIAIIPAYLDEIQSGLERSNQFYATRASEGGGADPWLEAGLKLSIQREVESSIYFMNNLKKGSSNVYLFDRQGNPYTAVKSGGVRSDLKEVYERWRQLAEPKNGTPVLVSTQAVTSSANSSKQYVFTVVRDIITTSFRSVGLIAVDANISVIEDMVRDLDEATRGTTIIADEGGTVIYDSEKRYLAENLGSAPLLAEARGSAGSYRTSVDGEEQLVIYRQSPDTGWKLLITIPQRHLVEDAVRNRNFSLIAAGVAMAAAMALTVVLILALTKPLRSLVSLMKQVQGGNFEVSFPVRRRDEAGMAGQAFNRMIARTRELIDNIYRIEQRKTEVQLENLQRQINPHFIYNTLESIRMTAVLSDADEVGRMVQLLGEQLRYSLHAGSAAVPAQREWEHLEQYVELMNYRYGGERFRLTLSAEARAADASVMKLIFQPIVENAVLHGYDDSRERLTIEIDSWIEGMDRVVRIRDDGRGMQPEVLARVRAELASAAAPLDEESGGIGLRNVQERLQLRYGPGYGLQLASEPGAGTTVTMRIPQIQAMDAPAEGEKRGEGADA
>NZ_CP045802.1|WP_028598937.1|5381255_5382767_-|response-regulator
MLKVAVVDDEEKIRLGLAKIIERTGPYEVVGVWASAREALSNLDASGAELLITDIRMPQMDGLQLIDELRERGSQIAVAVLSGYNDFAYAREALRGGVEDYLLKPVNQDELARLLERIAEKVGVSRSRQPLHAEALIELLLAADAKRIPEPVMQTACAQLDELGSIRGMYAFVVLHAAPMPDGERIAEALAALRREHRLLLREAGPPAVLLALRHGDHADTPRELAVTLLGRLPLSAEPRGGISGVHSGAAALARAYGEAEAALLQAWYAGSPAGTAVSAAASTPGRMPAAAQMPGAARPDEQELRAVLQAADLERAAAIAEEWLGAAEQRRLSWAELDAAAATLLGVLDDSLAGQPGPQPGSRPQPIRSRSWDAYAAALRQELQQRLALLGELKHQSRAVEAVKAYLQEHYADELDLQRLAELVHLTPSYLSKLFRSETGETITDYAISVRIEVAKRLLKDRPELKTYEVGERSGYADPAYFTKAFKRVTGKTPKEYRDSAR
>NZ_CP045802.1|WP_028598938.1|5379931_5380810_-|sugar-ABC-transporter-permease
MNQLSYKAQRRLILFGFLIVPVALCLTFSYYPAASLIYYSFTDWTGTGWDMNWVGLDNYKQIFTEPEVFLALKNNAYYFVGGLIQVALSLWFAVILTSRLKGRYGFRVMLFLPYVLHSVATVIMFKNVYHLDYGSLNSLLRTIGLESWQQSWLGNPHLVNVSLAFISMWKYMGLNMVIFIGALQSIPSDLYEAGSIDGASGWQKFRYITVPSIKSVLSLMLLLTLTGALEAFDIPYIMMLGANGTSTFVVQTVDTAFKYQSFGLASAMAVVLLIIVIFFIIIQRKVLFREER
>NZ_CP045802.1|WP_101807611.1|5379091_5379928_-|carbohydrate-ABC-transporter-permease
MDTTKSPPLFTAFKYLTLLIALFVVFFPIYSVFVGAFKTQAEFYQSSALAFPADFFHFDNFKRVYEVGDLGLGFRNTLVILVCAVAGNVVLGTMVAYALGRFDFKLKTPIMGMYLVAQVIPMVTTQVATFSIIQNLGLYNTMGAPILLYLGADVLQIVIYLQFVNSIPKDLDESAMIEGASLFRIYRSIIFPLLGPATATLVILKTISIYNDFYTPYLYMPSQKLKVVSTAIYSFVGPNAAQLNVISAGILIIFIPTVVLFLFLQKYIFAGVTNGAVK
>NZ_CP045802.1|WP_153784461.1|5378067_5379051_-|1,4-beta-xylanase
MTTQAKAAGSAAAAAELGYIAGMTWGWTGVRGTWEGPEADFSLSEMAKLNVGWTAVTLGALQATAQSTEIEYWNEPTVTDDEVRSAIRRAKALGQKVCLKPVVNVADGTWRAHINFFDMDIPGEPTWGQWFESYARFILHYADIAREEGCEMLCIGCEMVQADKREAEWRALIAQVREAYSGLVTYNCDKYQEGNVKWWDAVDLISSSGYYPIDQWEEQLDRIEAAVAPYGKPFFFMEAGCPSRDTSPARPNDWSLAGRPDGEAQRAYYEAMFGACGRREWVRGFVLWDWPARLYAAPDAAANDDYCMYGKPAAQTVKDFYGSRREG
>NZ_CP045802.1|WP_028598941.1|5376852_5378067_-|N-acyl-D-glucosamine-2-epimerase
MDKQAWLHELQQELQDNILGFWQTHALDELHGGFIGEMDSSGKVNPEADKSLVLNARILWTFAAAHRRTKNPQHLALAERALEQLRTVFYDELHGGFYWMATPDGRPSEDKKQVYGQSFVLYALAEYMLATGSTAELPLAEETYRLLERWAHDPVHRGYIEALARDWSETDDLSLSGKDLNERKSMNTHLHVLEGYTNLYRVWPSDGLRDRLRELIELHLERILDGETGHFKLFFDDEWNSATRDVSYGHDIEGSWLLCEAAEALGDPELLKQTERAALQMAEATLLEGVDEDGGVFNELHEDGRLDDSKDWWPQAEAMVGFLNAFQLSGEERYVQAAERSWSFIRQHVRDEDGGEWHWQVSRDGRPDRTQVKIGAWKCPYHNGRACLEALHRLESLTKEDALA
>NZ_CP045802.1|WP_028598942.1|5375405_5376728_-|extracellular-solute-binding-protein
MKKPLLVTMTAVLSLSMLAACGSNNNEGNANTAGNTSGSANTAANEGGSGGEAKLSGTIKMLTHRTDYINDGTMERYLKKFQEKYPDAKVEFEGLTNYATDIKTRLTTGETGDVLMIPSGMPASDLPKYFEPLPDSMFDDVYFADNSAFEGKRYGITTGVNTQGIVYNKKAFEKAGIAKAPTTLDELYDAAKKLKEAGIIPLYMNFGAQWPMGSWGDGSAFYVAGDADLTTKMAADPAPFQEGNAWGILAKIGRDFIKNGWVEKDLYTNNWEMSKGEIASGKAAMYFLGNWVIPQVIGAGAASEDIGFVPFPYDNSGKLNAPLGGDYMMGVSANSKNKELAIAWTDFFVKESGYVADSGFMPILKSEKAESPQLAEFQAANPTFIEGLPNNDKFAEIANKAQIGIGTGNYIQDLLLSKDLKAGLDELNKKWAKAKTDLGY
>NZ_CP045802.1|WP_052333269.1|5374000_5374780_-|aldo/keto-reductase
MPRLGLGVWKVTEEGQVEQAIRDAVKAGYRSIDTAKAYGNEEGVGRAIRECGVPREELFITTKVWNSDQGYESTLQAFQDSLDKLGLDTLDLYLIHWPVKGKYKDTWRALEQLYKDGKVRAIGVCNFHVHHLEDLLQDAEIKPMVNQVEYHPLLTQVELRQYCQDQGIVLEAWSPLMQGNLDVPQIQELAAKHGKTPAQIVLRWDLQNGVVTIPKSTHEKRIRENADVFDFELSHEDMALLDGLDQGKRFGPDPDNFNF
>NZ_CP045802.1|WP_028598945.1|5373432_5373858_-|Rrf2-family-transcriptional-regulator
MNSEFTIAVHSLVYLAYVPERSASSEAIAENVCTNPARVRKVMGYLKRCGYVATREGSGGGYRLTAEPSQVTLNDIYQAIARGSLMPNWCSGDPDCECLVGSNMQEVMNGIFCGAEQRLESYFQGLTIAGVLERIHRCETC
>NZ_CP045802.1|WP_153784462.1|5387292_5387559_+|hypothetical-protein
MTYVWAAIIVLAAGAVVYAAIASGKRWTLLRSESKARIDKLYRLEAHLKSNGVRTRTEEEDGHLRLLVLRKQLEQGRELLEAYEEETG
>NZ_CP045802.1|WP_153784463.1|5387809_5388562_+|DsbA-family-oxidoreductase
MTPLAHLPGGQALKPPSAWFILEGTIAGRRPRERRPPLLIEVYHDLLCPWCRIGRRHLELALREWQPPEGREASVRFSPYLLHPSVPPEGLPFREAMAQRLGGGQAALTRTLRHVARDGQAVGLDFRFERIATLPSTRLAHQALALTPAAAQGAFVDELSRRYFEEGENIGELEIVAQAGAAAGWEADGLADRLEQGDGRVEMEAMLELGRRIGQGGVPLFVFEGQYALSGAYPHSELLLLLRRLGQLLG
>NZ_CP045802.1|WP_153784464.1|5389410_5390406_-|glycosyltransferase
MHTEIQQAPGGIRSPEAPGSEAAGPVPAASVGDRVSVIIPTRNAGPDLEELLSRLSRQTLPPYEIIVIDTESTDGTPERAIRAGARLLSIARSEFDHGGARNRAAAEASGCILLFMTQDAMPADERLVEQLARSVGDPGVGYAYARQLARPEADLLERMSREHNYPAQSRLKSREDLSELGLKTFFCSNVCAATRRETFRTMGGFAEPTFFNEDLFLAGRMVLEGYRIAYNAEAQVVHSHAYTPGQQFKRFYDNGTSMAEQAWILPYAGVGKEGSSLVKAQLKALAQEGQWGKMPRLVADNAAKLIGYKLGIHHRRLPERLRRAFSMYRPG
>NZ_CP045802.1|WP_153784465.1|5390395_5391823_-|undecaprenyl-phosphate-glucose-phosphotransferase
MLRRNQRFLTQMYVLSDLAVMLGLFLGAYWIKFHSGLLVYYNTVPLKTYLVWSTVYAFAAVLIGFYTSFYTPKRRKKFSHDLLKIFQVQTLSLLLLLSLLFITKEVHISREFLAIFFAFNLVGLGLYRYALKRTLTVLRRRGLNKRYVLILGAGSVGRSFHDQLSLYPDLGYEAYGFLDDFHEEHDAAVLRRYSGRPLAPIVGRLDELERLLADNPTIDEVILALPLEAHSKYGELIQTCEKAGVKTLIIPDYFDLLPAKPFFDNFAGMPLINIRDVPLDEMGNRIAKRTFDIVFSLTALIALSPVMLLIALGIKLTSPGPVLFRQERVGLNRRSFAMLKFRSMRVSTDADASRTWTVENDPRRTRFGTFLRSTSLDELPQFLNVLRGEMSVVGPRPERPFFVDQFREEIPRYMVKHHIRPGITGWAQTNGLRGDTSIDERIRHDLFYIENWSFFFDIRIIFKTVLKGLIHKNAY
>NZ_CP045802.1|WP_153784466.1|5392095_5392911_+|ABC-transporter-permease
MFEILINQVRKCCPVNHFSRIINYRELLSELVKRDLKIKYRRSVLGVLWSILNPLLFMLITTMIFSTMFKNQIQNFPIYFLTGQIMYAFFAESTSMAQMGVLGNGSLIKKVYTPKYIFPLSKIIFSLVNTCYSLLAILIIFIIMGYSITLTALFFFIPILLLFIFSTGVGLFLSCMTVFYRDLLHIYSIILSLLSFFSATFYPIEIIPYPYRTFVEYNPVYVYIHYLRSLLIEGQFPDLTQNILAVAYSMVSLIIGFYIFNKNENKIVLHL
>NZ_CP045802.1|WP_153784467.1|5392921_5393656_+|ATP-binding-cassette-domain-containing-protein
MSNYAIKISDVSMVFDLHKENISSLKEMIIKRLKGQLQTEKFYALQNISLTIEKGEVAGILGFNGAGKSTLLKTIAGVLVPSTGKIETQGKIAPLIELGAGFDMELTARENIFLNGAILGYSRRFIQNKFDEIIDFAEIHDFLDVPLKNYSSGMIARIGFSIATVVKPDILIVDEILSVGDYKFQMKCEERIRTMIGDDTTVIMVSHSIEQIRTMCTKAFLLQQGRLIAQGEAAEICDIYMNSN
>NZ_CP045802.1|WP_153784468.1|5393696_5394752_+|NAD-dependent-epimerase/dehydratase-family-protein
MTRTCLITGGAGFIGCEVSKLIEDDFSSIIIMDSMHPQIHKSPEKPAALSLKANLYVSDITDPSAWDELLSKWKPDVVLHLAAETGTGQSLTESTRHASVNVVGTTQMLDAFVRNEIMPQKIVLASSRAVYGEGNWMNQDDSIYYPGQRTNEQLAREEWDFVESSFLPMRSASTLSMPTSIYGATKLTQENILTCWCNSFDVNYSILRFQNVYGPGQSLINSYTGIVSLFVRMAKQNESIPLYEDGLMIRDFVYISDVASAIREAMINPDANKKILDVGSGYGATIKEIAELIAIRYGAPQPFVCKKYRNGDVRHAQADISDTLATLNWTPEVTLNEGMNNLCDWIDLQLG
>NZ_CP045802.1|WP_153784469.1|5394775_5395684_+|glycosyltransferase-family-2-protein
MSQLRNLQIQSVLYHNEKSRIIRSIKSIVRAVDFSIHERIFDKVVVQYGDGSPAPIFTDEDLECLKKEYGEFIELKYEFFGENLGSARGHNRLASLSSTNFIMIINPDILLAPDTILELAKPFWESKNNIGIVEAKQLPIEHPKWFDPKSGATSWASTACVLMPRKAFDSVDGFDADTFFLYCDDVDFSWMLRKEGFQVLFQPSAVAFHDKTLSDEASWRTSSAEDYFSAEAGLLLAYKWSRIDILQNILAYFEQSDVDYYIKAAAEFRRREAAGILPKQYDTNHKIGEFSNNNYGKMRFVL
>NZ_CP045802.1|WP_153784470.1|5395680_5397513_+|methyltransferase-domain-containing-protein
MKRKSEIDYAYKFEYAFDNVYGHAFSLLKKFNFPKNGVHLDMGCGWGAISEKINELGLHYVGMDADPDATEHLRSIGRESHTFQFGLFKANIEAIETVLQGRPLASITVLDTLEHVLYYEELIKTISALSHKYGAPVVISVPNFAHDDVAFKLLCNRLDETSSGLLDETHINLFTAEKLLHTCKKNGLHQLAEKDVLLEKSDQYFPRDLLSLADASSLRQLLLNLRAGMNANGKVNQIVRLFVASHPSVLPAPESKRPFLTIVTRTTGDRAQELKEVLLCLTGQENTDFEVLIVGHNLTLDNQIKVENVIQSTPDWIRAKIRLIRINGGNRSAPLNAGFQEAQGEYISILDDDDIVFSNWIEQFYSLSKKNYGKILKSVSVRQEFEPVQTEYGSKASMAISSFHRDYPAEFDYLTMLHHNQCPGLCLAFPRSVYHDFGLRFDETINTVEDWDFILRATFICGVASSPVVTNIYRWWAKGNSSQTLHDSQEWTENYRHVQNKINQSYLILPPGNAKRISAMVDALSHGGPVSHPAQSEPQEMLWAKRDIAHQILSSDSWAVTKPLRIIKKWMGERTEVPNIFQSSEKELDDFIHHAQNSKSWRLTRFFRKS
>NZ_CP045802.1|WP_153784471.1|5397687_5398809_-|glycosyltransferase
MNIQDSAAQASPSPDKGGSGASQGSAAASVRATVSVHIVTYNSVDDIEGCLACVRAQSYPIEKIVVLDNASGDGTPELLGRIGEGLDVVLSPVNTGFAGGQNRALARSDADYALVLNPDVRLHPDYVRRLVESLERRPEAGSATGMLVRQPAEGLAGAPGVGGAEGGIAAPDEAGGGESPPAVQAWLDRLPAEALIDSTGLAMDAARQARDRGAGEPASAWLEAGETFGVSGAAAMYRRSMIRHVSLGGEFFDETFFAYKEDVDVAWRARGLGWAALYAPDARALHARGWKEGGRTSVSAFVRRHSYQNRFYTLVKNEREWRRLPAIVAIELAKFGYILLRERDLLRCWPEIMRRLPEMRAKRRELVAMKCLK

Crispr_ID: NZ_CP045802_25

• CRISPR_ID: NZ_CP045802_25
• CRISPR_location: 5386138-5386212
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP045802_25

Consensus_repeat	Method
GTCCGCCGCAGCGTCTCCGCCAG	CRISPRCasFinder

spacers of NZ_CP045802_25

>25.1|5386161|28|NZ_CP045802|CRISPRCasFinder
TGGTACATTTACCATATACGCGCCCCAT

CRISPR arrays and Neighbor proteins around NZ_CP045802_25

CRISPR arrays

The CRISPR arrays of NZ_CP045802_25

>merge|NZ_CP045802|25|5386138-5386212|CRISPRCasFinder
GTCCGCCGCAGCGTCTCCGCCAGTGGTACATTTACCATATACGCGCCCCATTTCCGCCGCAGCGTCTCCGCCAGC

>NZ_CP045802|25|20|5386138-5386212|CRISPRCasFinder
GTCCGCCGCAGCGTCTCCGCCAG	TGGTACATTTACCATATACGCGCCCCAT
TTCCGCCGCAGCGTCTCCGCCAGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_153784462.1|5387292_5387559_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028598935.1|5386305_5387178_-|DUF72-domain-containing-protein	unknown	unknown	gnl|CDD|224714
NZ_CP045802.1|WP_028598938.1|5379931_5380810_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP045802.1|WP_153784469.1|5394775_5395684_+|glycosyltransferase-family-2-protein	unknown	unknown	gnl|CDD|133029
NZ_CP045802.1|WP_153784468.1|5393696_5394752_+|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|187566
NZ_CP045802.1|WP_101807611.1|5379091_5379928_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP045802.1|WP_153784465.1|5390395_5391823_-|undecaprenyl-phosphate-glucose-phosphotransferase	unknown	unknown	gnl|CDD|274396
NZ_CP045802.1|WP_153784467.1|5392921_5393656_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213187
NZ_CP045802.1|WP_052333269.1|5374000_5374780_-|aldo/keto-reductase	unknown	unknown	gnl|CDD|381383
NZ_CP045802.1|WP_028598941.1|5376852_5378067_-|N-acyl-D-glucosamine-2-epimerase	unknown	unknown	gnl|CDD|238153
NZ_CP045802.1|WP_153784810.1|5384656_5385682_-|LacI-family-transcriptional-regulator	unknown	unknown	gnl|CDD|380629
NZ_CP045802.1|WP_052333243.1|5382759_5384664_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|225519
NZ_CP045802.1|WP_153784461.1|5378067_5379051_-|1,4-beta-xylanase	unknown	unknown	gnl|CDD|381624
NZ_CP045802.1|WP_028598945.1|5373432_5373858_-|Rrf2-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224870
NZ_CP045802.1|WP_028598937.1|5381255_5382767_-|response-regulator	unknown	unknown	gnl|CDD|381091
NZ_CP045802.1|WP_028598942.1|5375405_5376728_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270452
NZ_CP045802.1|WP_153784466.1|5392095_5392911_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|224596
NZ_CP045802.1|WP_153784470.1|5395680_5397513_+|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|132997
NZ_CP045802.1|WP_153784463.1|5387809_5388562_+|DsbA-family-oxidoreductase	unknown	unknown	gnl|CDD|239322
NZ_CP045802.1|WP_153784464.1|5389410_5390406_-|glycosyltransferase	unknown	unknown	gnl|CDD|366154

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_028598935.1|5386305_5387178_-|DUF72-domain-containing-protein	gnl|CDD|224714	COG1801, COG1801, Uncharacterized conserved protein [Function unknown].	2.24971e-71
NZ_CP045802.1|WP_028598938.1|5379931_5380810_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	3.25921e-72
NZ_CP045802.1|WP_153784469.1|5394775_5395684_+|glycosyltransferase-family-2-protein	gnl|CDD|133029	cd04186, GT_2_like_c, Subfamily of Glycosyltransferase Family GT2 of unknown function. GT-2 includes diverse families of glycosyltransferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	1.1981e-31
NZ_CP045802.1|WP_153784468.1|5393696_5394752_+|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|187566	cd05256, UDP_AE_SDR_e, UDP-N-acetylglucosamine 4-epimerase, extended (e) SDRs. This subgroup contains UDP-N-acetylglucosamine 4-epimerase of Pseudomonas aeruginosa, WbpP, an extended SDR, that catalyzes the NAD+ dependent conversion of UDP-GlcNAc and UDPGalNA to UDP-Glc and UDP-Gal. This subgroup has the characteristic active site tetrad and NAD-binding motif of the extended SDRs. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	1.52306e-59
NZ_CP045802.1|WP_101807611.1|5379091_5379928_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	8.79331e-57
NZ_CP045802.1|WP_153784465.1|5390395_5391823_-|undecaprenyl-phosphate-glucose-phosphotransferase	gnl|CDD|274396	TIGR03023, Sugar_transferase., Undecaprenyl-phosphate glucose phosphotransferase. This family of proteins encompasses the E. coli WcaJ protein involved in colanic acid biosynthesis, the Methylobacillus EpsB protein involved in methanolan biosynthesis, as well as the GumD protein involved in the biosynthesis of xanthan. All of these are closely related to the well-characterized WbaP (formerly RfbP) protein, which is the first enzyme in O-antigen biosynthesis in Salmonella typhimurium. The enzyme transfers galactose from UDP-galactose (NOTE: not glucose) to a polyprenyl carrier (utilizing the highly conserved C-terminal sugar transferase domain, pfam02397) a reaction which takes place at the cytoplasmic face of the inner membrane. The N-terminal hydrophobic domain is then believed to facilitate the "flippase" function of transferring the liposaccharide unit from the cytoplasmic face to the periplasmic face of the inner membrane. Most of these genes are found within large operons dedicated to the production of complex exopolysaccharides such as the enterobacterial O-antigen. Colanic acid biosynthesis utilizes a glucose-undecaprenyl carrier, knockout of EpsB abolishes incorporation of UDP-glucose into the lipid phase, and the C-terminal portion of GumD has been shown to be responsible for the glucosyl-1-transferase activity.	0
NZ_CP045802.1|WP_153784467.1|5392921_5393656_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|213187	cd03220, ABC_KpsT_Wzt, ATP-binding cassette component of polysaccharide transport system. The KpsT/Wzt ABC transporter subfamily is involved in extracellular polysaccharide export. Among the variety of membrane-linked or extracellular polysaccharides excreted by bacteria, only capsular polysaccharides, lipopolysaccharides, and teichoic acids have been shown to be exported by ABC transporters. A typical system is made of a conserved integral membrane and an ABC. In addition to these proteins, capsular polysaccharide exporter systems require two 'accessory' proteins to perform their function: a periplasmic (E.coli) or a lipid-anchored outer membrane protein called OMA (Neisseria meningitidis and Haemophilus influenza) and a cytoplasmic membrane protein MPA2.	6.98298e-100
NZ_CP045802.1|WP_052333269.1|5374000_5374780_-|aldo/keto-reductase	gnl|CDD|381383	cd19157, AKR_AKR5G1-3, AKR5G family of aldo-keto reductase (AKR). Bacillus subtilis glyoxal reductase (GR), uncharacterized oxidoreductase YtbE, and Bacillus aryabhattai aldo-keto reductase are founding members of aldo-keto reductase family 5 member G1-3 (AKR5G1-3), respectively. GR (YvgN, EC 1.1.1.283), also called methylglyoxal reductase, reduces glyoxal and methylglyoxal (2-oxopropanal). It is not involved in vitamin B6 biosynthesis.	3.26646e-171
NZ_CP045802.1|WP_028598941.1|5376852_5378067_-|N-acyl-D-glucosamine-2-epimerase	gnl|CDD|238153	cd00249, AGE, AGE domain; N-acyl-D-glucosamine 2-epimerase domain; Responsible for intermediate epimerization during biosynthesis of N-acetylneuraminic acid. Catalytic mechanism is believed to be via nucleotide elimination and readdition and is ATP modulated. AGE is structurally and mechanistically distinct from the other four types of epimerases. The AGE domain monomer is composed of an alpha(6)/alpha(6)-barrel, the structure of which is also found in glucoamylase and cellulase. The active form is a homodimer. The alignment also contains subtype III mannose 6-phosphate isomerases.	8.38586e-58
NZ_CP045802.1|WP_153784810.1|5384656_5385682_-|LacI-family-transcriptional-regulator	gnl|CDD|380629	cd19974, PBP1_LacI-like, ligand-binding domain of uncharacterized DNA-binding regulatory proteins that are members of the LacI-GalR family of bacterial transcription repressors. This group includes the ligand-binding domain of uncharacterized DNA-binding regulatory proteins that are members of the LacI-GalR family of bacterial transcription repressors. The LacI-GalR family repressors 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.	7.77189e-96
NZ_CP045802.1|WP_052333243.1|5382759_5384664_-|sensor-histidine-kinase	gnl|CDD|225519	COG2972, COG2972, Predicted signal transduction protein with a C-terminal ATPase domain [Signal transduction mechanisms].	8.4788e-53
NZ_CP045802.1|WP_153784461.1|5378067_5379051_-|1,4-beta-xylanase	gnl|CDD|381624	cd19606, GH113-like, Glycoside hydrolase family 113 beta-mannosidase and similar proteins. Family 113 glycoside hydrolases cleave (1->4)-beta-glycosidic linkages, such as endo-1,4-beta-mannanase. This family also includes TIM-barrel domains found in gene transfer agent proteins.	9.94199e-116
NZ_CP045802.1|WP_028598945.1|5373432_5373858_-|Rrf2-family-transcriptional-regulator	gnl|CDD|224870	COG1959, COG1959, Predicted transcriptional regulator [Transcription].	1.89174e-26
NZ_CP045802.1|WP_028598937.1|5381255_5382767_-|response-regulator	gnl|CDD|381091	cd17536, REC_YesN-like, phosphoacceptor receiver (REC) domain of YesN and related helix-turn-helix containing response regulators. This family is composed of uncharacterized response regulators that contain a REC domain and a AraC family helix-turn-helix (HTH) DNA-binding output domain, including Bacillus subtilis uncharacterized transcriptional regulatory protein YesN and Staphylococcus aureus uncharacterized response regulatory protein SAR0214. YesN is a member of the two-component regulatory system YesM/YesN and SAR0214 is a member of the probable two-component regulatory system SAR0215/SAR0214. Also included in this family is the AlgR-like group of LytTR/AlgR family response, which includes Pseudomonas aeruginosa positive alginate biosynthesis regulatory protein AlgR and Bacillus subtilis sensory transduction protein LytT, among others. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	7.46714e-44
NZ_CP045802.1|WP_028598942.1|5375405_5376728_-|extracellular-solute-binding-protein	gnl|CDD|270452	cd14749, PBP2_XBP1_like, The periplasmic-binding component of ABC transport systems specific for xylo-oligosaccharides; possesses type 2 periplasmic binding fold. This group represents the periplasmic component of an ABC transport system XBP1 that shows preference for xylo-oligosaccharides in the order of xylotriose > xylobiose > xylotetraose. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.40094e-36
NZ_CP045802.1|WP_153784466.1|5392095_5392911_+|ABC-transporter-permease	gnl|CDD|224596	COG1682, TagG, ABC-type polysaccharide/polyol phosphate export systems, permease component [Carbohydrate transport and metabolism / Cell envelope biogenesis, outer membrane].	1.05751e-48
NZ_CP045802.1|WP_153784470.1|5395680_5397513_+|methyltransferase-domain-containing-protein	gnl|CDD|132997	cd00761, Glyco_tranf_GTA_type, Glycosyltransferase family A (GT-A) includes diverse families of glycosyl transferases with a common GT-A type structural fold. Glycosyltransferases (GTs) are enzymes that synthesize oligosaccharides, polysaccharides, and glycoconjugates by transferring the sugar moiety from an activated nucleotide-sugar donor to an acceptor molecule, which may be a growing oligosaccharide, a lipid, or a protein. Based on the stereochemistry of the donor and acceptor molecules, GTs are classified as either retaining or inverting enzymes. To date, all GT structures adopt one of two possible folds, termed GT-A fold and GT-B fold. This hierarchy includes diverse families of glycosyl transferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. The majority of the proteins in this superfamily are Glycosyltransferase family 2 (GT-2) proteins. But it also includes families GT-43, GT-6, GT-8, GT13 and GT-7; which are evolutionarily related to GT-2 and share structure similarities.	2.09906e-11
NZ_CP045802.1|WP_153784463.1|5387809_5388562_+|DsbA-family-oxidoreductase	gnl|CDD|239322	cd03024, DsbA_FrnE, DsbA family, FrnE subfamily; FrnE is a DsbA-like protein containing a CXXC motif. It is presumed to be a thiol oxidoreductase involved in polyketide biosynthesis, specifically in the production of the aromatic antibiotics frenolicin and nanaomycins.	7.55722e-51
NZ_CP045802.1|WP_153784464.1|5389410_5390406_-|glycosyltransferase	gnl|CDD|366154	pfam00535, Glycos_transf_2, Glycosyl transferase family 2. Diverse family, transferring sugar from UDP-glucose, UDP-N-acetyl- galactosamine, GDP-mannose or CDP-abequose, to a range of substrates including cellulose, dolichol phosphate and teichoic acids.	3.24713e-24

Protein sequences

>NZ_CP045802.1|WP_153784810.1|5384656_5385682_-|LacI-family-transcriptional-regulator
MGHPEPSGSGQASGATAIGGQPGVPGFPAGEAGRFSPASSRAASNPAATQAASDGLGSQVIILVPNVRFQTRLSYYWGRIIEGVQEELEERGIGSILITEQGTTRFSSLINPRGVMGLVGVGFISYPVLLEIRNLGIPTVLIDHEEPLVPTDVLSMNNFEWMRRVANYLIGLGHRRLQFVGNLTYSRSFYDRWFGFRAMMEEHGLSTDGQHDGLLTVRGHNRSEMTEALEPMLQELRREGRMPTAFACANDSIAICIMTILARMGVSVPEDVSVAGFDDIEDAALSSPTLTTVHVHKHGMGRRAVEALLRRVQQPASPVEKVLLTGELVIRASTGAARADG
>NZ_CP045802.1|WP_052333243.1|5382759_5384664_-|sensor-histidine-kinase
MARLWSALRQQLEPLLHRLETRLLLVYFLLVLLPIAVITYVSASHNFATIEQNTVTYASQVSDRMLNSLDDYIHDMKQIAIIPAYLDEIQSGLERSNQFYATRASEGGGADPWLEAGLKLSIQREVESSIYFMNNLKKGSSNVYLFDRQGNPYTAVKSGGVRSDLKEVYERWRQLAEPKNGTPVLVSTQAVTSSANSSKQYVFTVVRDIITTSFRSVGLIAVDANISVIEDMVRDLDEATRGTTIIADEGGTVIYDSEKRYLAENLGSAPLLAEARGSAGSYRTSVDGEEQLVIYRQSPDTGWKLLITIPQRHLVEDAVRNRNFSLIAAGVAMAAAMALTVVLILALTKPLRSLVSLMKQVQGGNFEVSFPVRRRDEAGMAGQAFNRMIARTRELIDNIYRIEQRKTEVQLENLQRQINPHFIYNTLESIRMTAVLSDADEVGRMVQLLGEQLRYSLHAGSAAVPAQREWEHLEQYVELMNYRYGGERFRLTLSAEARAADASVMKLIFQPIVENAVLHGYDDSRERLTIEIDSWIEGMDRVVRIRDDGRGMQPEVLARVRAELASAAAPLDEESGGIGLRNVQERLQLRYGPGYGLQLASEPGAGTTVTMRIPQIQAMDAPAEGEKRGEGADA
>NZ_CP045802.1|WP_028598937.1|5381255_5382767_-|response-regulator
MLKVAVVDDEEKIRLGLAKIIERTGPYEVVGVWASAREALSNLDASGAELLITDIRMPQMDGLQLIDELRERGSQIAVAVLSGYNDFAYAREALRGGVEDYLLKPVNQDELARLLERIAEKVGVSRSRQPLHAEALIELLLAADAKRIPEPVMQTACAQLDELGSIRGMYAFVVLHAAPMPDGERIAEALAALRREHRLLLREAGPPAVLLALRHGDHADTPRELAVTLLGRLPLSAEPRGGISGVHSGAAALARAYGEAEAALLQAWYAGSPAGTAVSAAASTPGRMPAAAQMPGAARPDEQELRAVLQAADLERAAAIAEEWLGAAEQRRLSWAELDAAAATLLGVLDDSLAGQPGPQPGSRPQPIRSRSWDAYAAALRQELQQRLALLGELKHQSRAVEAVKAYLQEHYADELDLQRLAELVHLTPSYLSKLFRSETGETITDYAISVRIEVAKRLLKDRPELKTYEVGERSGYADPAYFTKAFKRVTGKTPKEYRDSAR
>NZ_CP045802.1|WP_028598938.1|5379931_5380810_-|sugar-ABC-transporter-permease
MNQLSYKAQRRLILFGFLIVPVALCLTFSYYPAASLIYYSFTDWTGTGWDMNWVGLDNYKQIFTEPEVFLALKNNAYYFVGGLIQVALSLWFAVILTSRLKGRYGFRVMLFLPYVLHSVATVIMFKNVYHLDYGSLNSLLRTIGLESWQQSWLGNPHLVNVSLAFISMWKYMGLNMVIFIGALQSIPSDLYEAGSIDGASGWQKFRYITVPSIKSVLSLMLLLTLTGALEAFDIPYIMMLGANGTSTFVVQTVDTAFKYQSFGLASAMAVVLLIIVIFFIIIQRKVLFREER
>NZ_CP045802.1|WP_101807611.1|5379091_5379928_-|carbohydrate-ABC-transporter-permease
MDTTKSPPLFTAFKYLTLLIALFVVFFPIYSVFVGAFKTQAEFYQSSALAFPADFFHFDNFKRVYEVGDLGLGFRNTLVILVCAVAGNVVLGTMVAYALGRFDFKLKTPIMGMYLVAQVIPMVTTQVATFSIIQNLGLYNTMGAPILLYLGADVLQIVIYLQFVNSIPKDLDESAMIEGASLFRIYRSIIFPLLGPATATLVILKTISIYNDFYTPYLYMPSQKLKVVSTAIYSFVGPNAAQLNVISAGILIIFIPTVVLFLFLQKYIFAGVTNGAVK
>NZ_CP045802.1|WP_153784461.1|5378067_5379051_-|1,4-beta-xylanase
MTTQAKAAGSAAAAAELGYIAGMTWGWTGVRGTWEGPEADFSLSEMAKLNVGWTAVTLGALQATAQSTEIEYWNEPTVTDDEVRSAIRRAKALGQKVCLKPVVNVADGTWRAHINFFDMDIPGEPTWGQWFESYARFILHYADIAREEGCEMLCIGCEMVQADKREAEWRALIAQVREAYSGLVTYNCDKYQEGNVKWWDAVDLISSSGYYPIDQWEEQLDRIEAAVAPYGKPFFFMEAGCPSRDTSPARPNDWSLAGRPDGEAQRAYYEAMFGACGRREWVRGFVLWDWPARLYAAPDAAANDDYCMYGKPAAQTVKDFYGSRREG
>NZ_CP045802.1|WP_028598941.1|5376852_5378067_-|N-acyl-D-glucosamine-2-epimerase
MDKQAWLHELQQELQDNILGFWQTHALDELHGGFIGEMDSSGKVNPEADKSLVLNARILWTFAAAHRRTKNPQHLALAERALEQLRTVFYDELHGGFYWMATPDGRPSEDKKQVYGQSFVLYALAEYMLATGSTAELPLAEETYRLLERWAHDPVHRGYIEALARDWSETDDLSLSGKDLNERKSMNTHLHVLEGYTNLYRVWPSDGLRDRLRELIELHLERILDGETGHFKLFFDDEWNSATRDVSYGHDIEGSWLLCEAAEALGDPELLKQTERAALQMAEATLLEGVDEDGGVFNELHEDGRLDDSKDWWPQAEAMVGFLNAFQLSGEERYVQAAERSWSFIRQHVRDEDGGEWHWQVSRDGRPDRTQVKIGAWKCPYHNGRACLEALHRLESLTKEDALA
>NZ_CP045802.1|WP_028598942.1|5375405_5376728_-|extracellular-solute-binding-protein
MKKPLLVTMTAVLSLSMLAACGSNNNEGNANTAGNTSGSANTAANEGGSGGEAKLSGTIKMLTHRTDYINDGTMERYLKKFQEKYPDAKVEFEGLTNYATDIKTRLTTGETGDVLMIPSGMPASDLPKYFEPLPDSMFDDVYFADNSAFEGKRYGITTGVNTQGIVYNKKAFEKAGIAKAPTTLDELYDAAKKLKEAGIIPLYMNFGAQWPMGSWGDGSAFYVAGDADLTTKMAADPAPFQEGNAWGILAKIGRDFIKNGWVEKDLYTNNWEMSKGEIASGKAAMYFLGNWVIPQVIGAGAASEDIGFVPFPYDNSGKLNAPLGGDYMMGVSANSKNKELAIAWTDFFVKESGYVADSGFMPILKSEKAESPQLAEFQAANPTFIEGLPNNDKFAEIANKAQIGIGTGNYIQDLLLSKDLKAGLDELNKKWAKAKTDLGY
>NZ_CP045802.1|WP_052333269.1|5374000_5374780_-|aldo/keto-reductase
MPRLGLGVWKVTEEGQVEQAIRDAVKAGYRSIDTAKAYGNEEGVGRAIRECGVPREELFITTKVWNSDQGYESTLQAFQDSLDKLGLDTLDLYLIHWPVKGKYKDTWRALEQLYKDGKVRAIGVCNFHVHHLEDLLQDAEIKPMVNQVEYHPLLTQVELRQYCQDQGIVLEAWSPLMQGNLDVPQIQELAAKHGKTPAQIVLRWDLQNGVVTIPKSTHEKRIRENADVFDFELSHEDMALLDGLDQGKRFGPDPDNFNF
>NZ_CP045802.1|WP_028598945.1|5373432_5373858_-|Rrf2-family-transcriptional-regulator
MNSEFTIAVHSLVYLAYVPERSASSEAIAENVCTNPARVRKVMGYLKRCGYVATREGSGGGYRLTAEPSQVTLNDIYQAIARGSLMPNWCSGDPDCECLVGSNMQEVMNGIFCGAEQRLESYFQGLTIAGVLERIHRCETC
>NZ_CP045802.1|WP_028598935.1|5386305_5387178_-|DUF72-domain-containing-protein
MITIGLAGWGDHDSLYRTREAAKAKLAAYSRLFGTVEVDSSFYAVQPQRNMEKWTAETPEDFRFVVKAYQGMTGHSRGAIPYPDEEAMFADFKLALTPMRESGKLSCVLFQYPPWFACTRESVETLRKAKRLMEDIPCALEFRHQSWFVPQMRERTLGFMREEGWRHSVCDEPQAGEGSIPIVEAATDESHTLVRMHGRHAEGWHSSGQPNWREVRYLYRYSRQELEEWAERLRRLEAQSRTVEVIFNNNSGGDAADNARELMALLGQTPPPIPEEPPERDPGVEQLELF
>NZ_CP045802.1|WP_153784462.1|5387292_5387559_+|hypothetical-protein
MTYVWAAIIVLAAGAVVYAAIASGKRWTLLRSESKARIDKLYRLEAHLKSNGVRTRTEEEDGHLRLLVLRKQLEQGRELLEAYEEETG
>NZ_CP045802.1|WP_153784463.1|5387809_5388562_+|DsbA-family-oxidoreductase
MTPLAHLPGGQALKPPSAWFILEGTIAGRRPRERRPPLLIEVYHDLLCPWCRIGRRHLELALREWQPPEGREASVRFSPYLLHPSVPPEGLPFREAMAQRLGGGQAALTRTLRHVARDGQAVGLDFRFERIATLPSTRLAHQALALTPAAAQGAFVDELSRRYFEEGENIGELEIVAQAGAAAGWEADGLADRLEQGDGRVEMEAMLELGRRIGQGGVPLFVFEGQYALSGAYPHSELLLLLRRLGQLLG
>NZ_CP045802.1|WP_153784464.1|5389410_5390406_-|glycosyltransferase
MHTEIQQAPGGIRSPEAPGSEAAGPVPAASVGDRVSVIIPTRNAGPDLEELLSRLSRQTLPPYEIIVIDTESTDGTPERAIRAGARLLSIARSEFDHGGARNRAAAEASGCILLFMTQDAMPADERLVEQLARSVGDPGVGYAYARQLARPEADLLERMSREHNYPAQSRLKSREDLSELGLKTFFCSNVCAATRRETFRTMGGFAEPTFFNEDLFLAGRMVLEGYRIAYNAEAQVVHSHAYTPGQQFKRFYDNGTSMAEQAWILPYAGVGKEGSSLVKAQLKALAQEGQWGKMPRLVADNAAKLIGYKLGIHHRRLPERLRRAFSMYRPG
>NZ_CP045802.1|WP_153784465.1|5390395_5391823_-|undecaprenyl-phosphate-glucose-phosphotransferase
MLRRNQRFLTQMYVLSDLAVMLGLFLGAYWIKFHSGLLVYYNTVPLKTYLVWSTVYAFAAVLIGFYTSFYTPKRRKKFSHDLLKIFQVQTLSLLLLLSLLFITKEVHISREFLAIFFAFNLVGLGLYRYALKRTLTVLRRRGLNKRYVLILGAGSVGRSFHDQLSLYPDLGYEAYGFLDDFHEEHDAAVLRRYSGRPLAPIVGRLDELERLLADNPTIDEVILALPLEAHSKYGELIQTCEKAGVKTLIIPDYFDLLPAKPFFDNFAGMPLINIRDVPLDEMGNRIAKRTFDIVFSLTALIALSPVMLLIALGIKLTSPGPVLFRQERVGLNRRSFAMLKFRSMRVSTDADASRTWTVENDPRRTRFGTFLRSTSLDELPQFLNVLRGEMSVVGPRPERPFFVDQFREEIPRYMVKHHIRPGITGWAQTNGLRGDTSIDERIRHDLFYIENWSFFFDIRIIFKTVLKGLIHKNAY
>NZ_CP045802.1|WP_153784466.1|5392095_5392911_+|ABC-transporter-permease
MFEILINQVRKCCPVNHFSRIINYRELLSELVKRDLKIKYRRSVLGVLWSILNPLLFMLITTMIFSTMFKNQIQNFPIYFLTGQIMYAFFAESTSMAQMGVLGNGSLIKKVYTPKYIFPLSKIIFSLVNTCYSLLAILIIFIIMGYSITLTALFFFIPILLLFIFSTGVGLFLSCMTVFYRDLLHIYSIILSLLSFFSATFYPIEIIPYPYRTFVEYNPVYVYIHYLRSLLIEGQFPDLTQNILAVAYSMVSLIIGFYIFNKNENKIVLHL
>NZ_CP045802.1|WP_153784467.1|5392921_5393656_+|ATP-binding-cassette-domain-containing-protein
MSNYAIKISDVSMVFDLHKENISSLKEMIIKRLKGQLQTEKFYALQNISLTIEKGEVAGILGFNGAGKSTLLKTIAGVLVPSTGKIETQGKIAPLIELGAGFDMELTARENIFLNGAILGYSRRFIQNKFDEIIDFAEIHDFLDVPLKNYSSGMIARIGFSIATVVKPDILIVDEILSVGDYKFQMKCEERIRTMIGDDTTVIMVSHSIEQIRTMCTKAFLLQQGRLIAQGEAAEICDIYMNSN
>NZ_CP045802.1|WP_153784468.1|5393696_5394752_+|NAD-dependent-epimerase/dehydratase-family-protein
MTRTCLITGGAGFIGCEVSKLIEDDFSSIIIMDSMHPQIHKSPEKPAALSLKANLYVSDITDPSAWDELLSKWKPDVVLHLAAETGTGQSLTESTRHASVNVVGTTQMLDAFVRNEIMPQKIVLASSRAVYGEGNWMNQDDSIYYPGQRTNEQLAREEWDFVESSFLPMRSASTLSMPTSIYGATKLTQENILTCWCNSFDVNYSILRFQNVYGPGQSLINSYTGIVSLFVRMAKQNESIPLYEDGLMIRDFVYISDVASAIREAMINPDANKKILDVGSGYGATIKEIAELIAIRYGAPQPFVCKKYRNGDVRHAQADISDTLATLNWTPEVTLNEGMNNLCDWIDLQLG
>NZ_CP045802.1|WP_153784469.1|5394775_5395684_+|glycosyltransferase-family-2-protein
MSQLRNLQIQSVLYHNEKSRIIRSIKSIVRAVDFSIHERIFDKVVVQYGDGSPAPIFTDEDLECLKKEYGEFIELKYEFFGENLGSARGHNRLASLSSTNFIMIINPDILLAPDTILELAKPFWESKNNIGIVEAKQLPIEHPKWFDPKSGATSWASTACVLMPRKAFDSVDGFDADTFFLYCDDVDFSWMLRKEGFQVLFQPSAVAFHDKTLSDEASWRTSSAEDYFSAEAGLLLAYKWSRIDILQNILAYFEQSDVDYYIKAAAEFRRREAAGILPKQYDTNHKIGEFSNNNYGKMRFVL
>NZ_CP045802.1|WP_153784470.1|5395680_5397513_+|methyltransferase-domain-containing-protein
MKRKSEIDYAYKFEYAFDNVYGHAFSLLKKFNFPKNGVHLDMGCGWGAISEKINELGLHYVGMDADPDATEHLRSIGRESHTFQFGLFKANIEAIETVLQGRPLASITVLDTLEHVLYYEELIKTISALSHKYGAPVVISVPNFAHDDVAFKLLCNRLDETSSGLLDETHINLFTAEKLLHTCKKNGLHQLAEKDVLLEKSDQYFPRDLLSLADASSLRQLLLNLRAGMNANGKVNQIVRLFVASHPSVLPAPESKRPFLTIVTRTTGDRAQELKEVLLCLTGQENTDFEVLIVGHNLTLDNQIKVENVIQSTPDWIRAKIRLIRINGGNRSAPLNAGFQEAQGEYISILDDDDIVFSNWIEQFYSLSKKNYGKILKSVSVRQEFEPVQTEYGSKASMAISSFHRDYPAEFDYLTMLHHNQCPGLCLAFPRSVYHDFGLRFDETINTVEDWDFILRATFICGVASSPVVTNIYRWWAKGNSSQTLHDSQEWTENYRHVQNKINQSYLILPPGNAKRISAMVDALSHGGPVSHPAQSEPQEMLWAKRDIAHQILSSDSWAVTKPLRIIKKWMGERTEVPNIFQSSEKELDDFIHHAQNSKSWRLTRFFRKS

Crispr_ID: NZ_CP045802_27

• CRISPR_ID: NZ_CP045802_27
• CRISPR_location: 5556304-5556482
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 3 spacers

Consensus repeat of NZ_CP045802_27

Consensus_repeat	Method
GCCTCGGAAATCCGGGCTC	CRT

spacers of NZ_CP045802_27

>27.1|5556323|34|NZ_CP045802|CRT
CGATATAGCGGGCGGAGCCGGCTGGAGGAGGTTG
>27.2|5556376|35|NZ_CP045802|CRT
GCGTACAGAGGCGCCAGCCTTGGACAGCCAGGTTA
>27.3|5556430|34|NZ_CP045802|CRT
CGATATAGCAGGCGGAGCCGGCTGGAGGGCGTTA

CRISPR arrays and Neighbor proteins around NZ_CP045802_27

CRISPR arrays

The CRISPR arrays of NZ_CP045802_27

>merge|NZ_CP045802|27|5556304-5556482|CRT
GTGCCACTAATCCGGGCTCCGATATAGCGGGCGGAGCCGGCTGGAGGAGGTTGGCCTCGGAAGTCCGGGCTGGCGTACAGAGGCGCCAGCCTTGGACAGCCAGGTTAGCCTCGGAAATCCGGGCTCCGATATAGCAGGCGGAGCCGGCTGGAGGGCGTTAGCCTCGGAAATCCGGGCTC

>NZ_CP045802|27|8|5556304-5556482|CRT
GTGCCACTAATCCGGGCTC	CGATATAGCGGGCGGAGCCGGCTGGAGGAGGTTG
GCCTCGGAAGTCCGGGCTG	GCGTACAGAGGCGCCAGCCTTGGACAGCCAGGTTA
GCCTCGGAAATCCGGGCTC	CGATATAGCAGGCGGAGCCGGCTGGAGGGCGTTA
GCCTCGGAAATCCGGGCTC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_052333212.1|5552015_5553161_-|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|378964
NZ_CP045802.1|WP_028598843.1|5554674_5556222_-|L-glutamate-gamma-semialdehyde-dehydrogenase	unknown	unknown	gnl|CDD|179543
NZ_CP045802.1|WP_028598846.1|5549715_5550693_-|aromatic-ring-hydroxylating-dioxygenase-subunit-alpha	unknown	unknown	gnl|CDD|226985
NZ_CP045802.1|WP_101807556.1|5562693_5564040_-|glycosyltransferase-family-4-protein	unknown	unknown	gnl|CDD|340831
NZ_CP045802.1|WP_028598837.1|5572021_5572930_-|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223656
NZ_CP045802.1|WP_084137206.1|5546230_5547142_-|M23-family-metallopeptidase	unknown	unknown	gnl|CDD|366703
NZ_CP045802.1|WP_028598847.1|5548970_5549585_+|DedA-family-protein	unknown	unknown	gnl|CDD|223659
NZ_CP045802.1|WP_101807558.1|5558481_5560443_+|PAS-domain-S-box-protein	unknown	unknown	gnl|CDD|226350
NZ_CP045802.1|WP_028598850.1|5543973_5545434_+|catalase	unknown	unknown	gnl|CDD|163710
NZ_CP045802.1|WP_153784526.1|5575286_5577047_-|HAMP-domain-containing-protein	unknown	unknown	gnl|CDD|223910
NZ_CP045802.1|WP_101807557.1|5561068_5562697_-|cupin-domain-containing-protein	unknown	unknown	gnl|CDD|133003
NZ_CP045802.1|WP_153784525.1|5568710_5571749_-|MMPL-family-transporter	unknown	unknown	gnl|CDD|223911
NZ_CP045802.1|WP_127464548.1|5547183_5548515_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_101807554.1|5573134_5575204_-|catalase	unknown	unknown	gnl|CDD|236886
NZ_CP045802.1|WP_028598842.1|5557330_5558254_+|proline-dehydrogenase	unknown	unknown	gnl|CDD|223580
NZ_CP045802.1|WP_028598849.1|5545621_5546161_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_101807561.1|5550720_5551848_-|BMP-family-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|380618
NZ_CP045802.1|WP_028598839.1|5567393_5568587_+|glycosyltransferase-family-1-protein	unknown	unknown	gnl|CDD|340842
NZ_CP045802.1|WP_101807560.1|5553283_5554615_-|RNA-polymerase-factor-sigma-54	unknown	unknown	gnl|CDD|274109
NZ_CP045802.1|WP_028598840.1|5565404_5566637_+|peptidase-T	unknown	unknown	gnl|CDD|235484

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_052333212.1|5552015_5553161_-|AraC-family-transcriptional-regulator	gnl|CDD|378964	pfam12833, HTH_18, Helix-turn-helix domain.	5.78252e-20
NZ_CP045802.1|WP_028598843.1|5554674_5556222_-|L-glutamate-gamma-semialdehyde-dehydrogenase	gnl|CDD|179543	PRK03137, PRK03137, 1-pyrroline-5-carboxylate dehydrogenase; Provisional.	0
NZ_CP045802.1|WP_028598846.1|5549715_5550693_-|aromatic-ring-hydroxylating-dioxygenase-subunit-alpha	gnl|CDD|226985	COG4638, HcaE, Phenylpropionate dioxygenase and related ring-hydroxylating dioxygenases, large terminal subunit [Inorganic ion transport and metabolism / General function prediction only].	1.4019e-41
NZ_CP045802.1|WP_101807556.1|5562693_5564040_-|glycosyltransferase-family-4-protein	gnl|CDD|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	3.99307e-27
NZ_CP045802.1|WP_084137206.1|5546230_5547142_-|M23-family-metallopeptidase	gnl|CDD|366703	pfam01551, Peptidase_M23, Peptidase family M23. Members of this family are zinc metallopeptidases with a range of specificities. The peptidase family M23 is included in this family, these are Gly-Gly endopeptidases. Peptidase family M23 are also endopeptidases. This family also includes some bacterial lipoproteins for which no proteolytic activity has been demonstrated. This family also includes leukocyte cell-derived chemotaxin 2 (LECT2) proteins. LECT2 is a liver-specific protein which is thought to be linked to hepatocyte growth although the exact function of this protein is unknown.	6.80789e-10
NZ_CP045802.1|WP_028598847.1|5548970_5549585_+|DedA-family-protein	gnl|CDD|223659	COG0586, DedA, Uncharacterized membrane-associated protein [Function unknown].	1.00785e-45
NZ_CP045802.1|WP_101807558.1|5558481_5560443_+|PAS-domain-S-box-protein	gnl|CDD|226350	COG3829, RocR, Transcriptional regulator containing PAS, AAA-type ATPase, and DNA-binding domains [Transcription / Signal transduction mechanisms].	6.95456e-136
NZ_CP045802.1|WP_028598850.1|5543973_5545434_+|catalase	gnl|CDD|163710	cd08154, catalase_clade_1, Clade 1 of the heme-binding enzyme catalase. Catalase is a ubiquitous enzyme found in both prokaryotes and eukaryotes, which is involved in the protection of cells from the toxic effects of peroxides. It catalyzes the conversion of hydrogen peroxide to water and molecular oxygen. Catalases also utilize hydrogen peroxide to oxidize various substrates such as alcohol or phenols. Clade 1 catalases are found in bacteria, algae, and plants; they have a relatively small subunit size of 55 to 69 kDa, and bind a protoheme IX (heme b) group buried deep inside the structure. They appear to form tetramers. In eukaryotic cells, catalases are located in peroxisomes.	0
NZ_CP045802.1|WP_153784526.1|5575286_5577047_-|HAMP-domain-containing-protein	gnl|CDD|223910	COG0840, Tar, Methyl-accepting chemotaxis protein [Cell motility and secretion / Signal transduction mechanisms].	9.30268e-50
NZ_CP045802.1|WP_101807557.1|5561068_5562697_-|cupin-domain-containing-protein	gnl|CDD|133003	cd02509, GDP-M1P_Guanylyltransferase, GDP-M1P_Guanylyltransferase catalyzes the formation of GDP-Mannose. GDP-mannose-1-phosphate guanylyltransferase, also called GDP-mannose pyrophosphorylase (GDP-MP), catalyzes the formation of GDP-Mannose from mannose-1-phosphate and GTP. Mannose is a key monosaccharide for glycosylation of proteins and lipids. GDP-Mannose is the activated donor for mannosylation of various biomolecules. This enzyme is known to be bifunctional, as both mannose-6-phosphate isomerase and mannose-1-phosphate guanylyltransferase. This CD covers the N-terminal GDP-mannose-1-phosphate guanylyltransferase domain, whereas the isomerase function is located at the C-terminal half. GDP-MP is a member of the nucleotidyltransferase family of enzymes.	5.10162e-30
NZ_CP045802.1|WP_153784525.1|5568710_5571749_-|MMPL-family-transporter	gnl|CDD|223911	COG0841, AcrB, Cation/multidrug efflux pump [Defense mechanisms].	0
NZ_CP045802.1|WP_028598837.1|5572021_5572930_-|LysR-family-transcriptional-regulator	gnl|CDD|223656	COG0583, LysR, Transcriptional regulator [Transcription].	9.52066e-28
NZ_CP045802.1|WP_101807554.1|5573134_5575204_-|catalase	gnl|CDD|236886	PRK11249, katE, hydroperoxidase II; Provisional.	0
NZ_CP045802.1|WP_028598842.1|5557330_5558254_+|proline-dehydrogenase	gnl|CDD|223580	COG0506, PutA, Proline dehydrogenase [Amino acid transport and metabolism].	3.00752e-47
NZ_CP045802.1|WP_101807561.1|5550720_5551848_-|BMP-family-ABC-transporter-substrate-binding-protein	gnl|CDD|380618	cd19963, PBP1_BMP-like, periplasmic binding component of a basic membrane lipoprotein (BMP) from Brucella abortus and its close homologs in other bacteria. Periplasmic binding component of a family of basic membrane lipoproteins from Borrelia and various putative lipoproteins from other bacteria. These outer membrane proteins include Med, a cell-surface localized protein regulating the competence transcription factor gene comK in Bacillus subtilis, and PnrA, a periplasmic purine nucleoside binding protein of an ATP-binding cassette (ABC) transport system in Treponema pallidum. All contain the type 1 periplasmic sugar-binding protein-like fold.	1.17035e-151
NZ_CP045802.1|WP_028598839.1|5567393_5568587_+|glycosyltransferase-family-1-protein	gnl|CDD|340842	cd03814, GT4-like, glycosyltransferase family 4 proteins. This family is most closely related to the GT4 family of glycosyltransferases and includes a sequence annotated as alpha-D-mannose-alpha(1-6)phosphatidyl myo-inositol monomannoside transferase from Bacillus halodurans. Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in bacteria and eukaryotes.	2.32936e-142
NZ_CP045802.1|WP_101807560.1|5553283_5554615_-|RNA-polymerase-factor-sigma-54	gnl|CDD|274109	TIGR02395, RNA_polymerase_sigma-54_factor, RNA polymerase sigma-54 factor. A sigma factor is a DNA-binding protein protein that binds to the DNA-directed RNA polymerase core to produce the holoenzyme capable of initiating transcription at specific sites. Different sigma factors act in vegetative growth, heat shock, extracytoplasmic functions (ECF), etc. This model represents the clade of sigma factors called sigma-54, or RpoN (unrelated to sigma 70-type factors such as RpoD/SigA). RpoN is responsible for enhancer-dependent transcription, and its presence characteristically is associated with varied panels of activators, most of which are enhancer-binding proteins (but see Brahmachary, et al., ). RpoN may be responsible for transcription of nitrogen fixation genes, flagellins, pilins, etc., and synonyms for the gene symbol rpoN, such as ntrA, reflect these observations [Transcription, Transcription factors].	1.98115e-122
NZ_CP045802.1|WP_028598840.1|5565404_5566637_+|peptidase-T	gnl|CDD|235484	PRK05469, PRK05469, tripeptide aminopeptidase PepT.	0

Protein sequences

>NZ_CP045802.1|WP_028598843.1|5554674_5556222_-|L-glutamate-gamma-semialdehyde-dehydrogenase
MRMEYANEPFTNFSKEEESAAYEAALAAVRGQLGRTYPIVIGGEAIETGRTLDSINPADKAEVVGVVHQADRELAEKAIRTAYETFGWWRHTSAKERSGYLFKAAAVMRRRKHEFSAWLTVESGKNRAEADADTAEAIDFMEFYAREMLRLSEPQPLTRIPDEDNELYYIPLGVGIVIPPWNFPLAIMAGMTTAALVSGNTVVLKPASPTAVIAAKFVELLEEVGVPAGVVNFLPGPGSEVGDFLVEHPLTRFISFTGSRDVGLRINERAAKTAPGQKWIKRVIAEMGGKDSIVVDADADLELAADAIAASAFGFSGQKCSACSRAIVHADVYDEVLAKVVERTAKLTLGDPAERGTNLGPVVDDKAYAKIQEYIEIGKNEGRLVHGGGTGDEKGFFIEPTIFADIAPEARLAQEEIFGPVVAFIKASTFDEALEIANNTDYGLTGAVISRNRSRLEQARREFFAGNLYFNRKCTGALVGVHPFGGFNMSGTDSKAGGRDYLLLFTQAKLVSEKM
>NZ_CP045802.1|WP_101807560.1|5553283_5554615_-|RNA-polymerase-factor-sigma-54
MPGPVLQPQALLRQEQRQKLALTQQMRQSLALLALPAAELDRAVRELAADNPLLEIREPAASRRLGGRGHASAADPLERAAAAPPTLEAELLAQLRLSGAPAPLRRAAAWLAGNLDESGWLALPLAEAAERLRLSAAEAEAALRLLQSLQPAGIGARDLRECLLLQLDREPEPAPGARELAARWLPQLAARRWEEIAAGTGLSRAQLEEARRALLRLDPRPGQRLAAGAAGRTQAVVPDALVRQGADGELLVELAAAWEPRLSLADIGSGPLAAVARGHEAYAYVESCRRAARALIGGLEQRRETLARVVRAVFEEQAAFLERGWPALRPLTLADVALRLGLHESTVSRAVSGKQVRTPLGTYPLKAFFSAALGRGGAAEEVSAAAAKQRLAELVAAECRERPLSDQQLAERLAELGIPLSRRTVAKYRAELRIPSSSSRRGD
>NZ_CP045802.1|WP_052333212.1|5552015_5553161_-|AraC-family-transcriptional-regulator
MDDRELLPLNNRAIFEPRAAAQSFRLQRLLPQGPAAAYIRHYWLIEWNLPPGAVHTQEVLEHPTVNVVLQPGRSVVSVAGAERSQQRLEGRDEVLGMLFRPGLFRRWLDRDPGELAGRRLPAEQVLGPGVLELERAVFAEPDSSRRAALVDAFWAERLAEPGTLPCFRTTSDPTSDPPSDPEPDPTSDPPSDPEPDPTSDPTPDPTFDPASDPTPASAPPAPVPSGSVSFAPASLGAAPETDPSKMAPSRSAAPGTDHSKRAPSGSASLAPDPSAQLADRIVTGIQLDRSQRSAREVAARWGLSPRSLQRLFRAYIGMTPQAVIRRYRLHETMGLASGDPDWASLALELGYFDQAHLIRDFKAVVGMTPGSYAKRITSEER
>NZ_CP045802.1|WP_101807561.1|5550720_5551848_-|BMP-family-ABC-transporter-substrate-binding-protein
MLAILLVLGACSGGGGAANEGAGPTSVPSAGEPAGASPAPAGGGIAKPRVAFVYLGVPGDGGWTYEHDQGRLMMEKELGIEATTVENVPEGADAERVFEELAQNHDVVFGTSFGYMDAMVNVAKRHPDVKFMHASGYKTADNLGTYLGKEYQSAYLVGMAAGKMTKNDHLGYVGAYPIPEVIYTINAFALGAQSVNPDIKLSVVWSNTWYDPATERQAAVSLLDKGVDVLAAYQDSPASIQAAAERGVWGIGNDSDMGRYAPETYISNPVWRWGPYYVEQVKAVIDGTWQSGSYFGSMADGITDIAPFGKNVPEDVKALAEEKKQEILAGSFDVFAGPIRDQSGAERVPEGGAMTVEDILGMTWFVEGIEGTIPQ
>NZ_CP045802.1|WP_028598846.1|5549715_5550693_-|aromatic-ring-hydroxylating-dioxygenase-subunit-alpha
MRLEDPVLTACWHPAALARDVTDRPYPVTVLGEKLVLFRSGSGVHALKDLCIHRGVPLSLGKVDRGELVCAYHGWRYDGGGACVCIPSLPPRQPIPSKARAEAYRCREEGGFVWVCLGEAEPERLPLQGKVDPALIPVWMGPYPVQAAAPRVVENFLDVSHLMFVHEGLLGDSRHAEINDYGVHRREDALFTDEIVVYQPDPDGRGVGVESRYVYEIFGPTCVKLVKRSSGSDEEFHLFLIVLPETATACTAFMLQLRNYSPNVPEQVFIDFQNTLLAQDKVIVEAQKPELLPLDLQAELHLRSDRVAIAYRRMLREQGMTIGTE
>NZ_CP045802.1|WP_028598847.1|5548970_5549585_+|DedA-family-protein
MEAWITEIMDRFGYFGVGFLIAIENLFPPIPSEVILTFGGFMTARTSMTVVGVIIAATLGSVIGAVILYYIGAWLNAERLERIVARWGHILRLKPEDVRKADAWFDRYGPWAVLLCRLVPLVRSLISIPAGMSGMSFPLFLLLTTIGSLIWNTVLVSVGASVGESWETIVGYMDIYSNIAYALIALGVLAGAFWFYRSRRKAGR
>NZ_CP045802.1|WP_127464548.1|5547183_5548515_-|hypothetical-protein
MKKSTITIVLTSALILVGAATSHIIQASAPNGPDPYQLEAVPYEGQISKVMRGESGSSLLVDSIGSNEYSKMMSILYPNGIVDAQGQEVPGIDNLVEVRERFIEEHMRALSLVGSTPIEIEKTPFTISIADESNGEYKSLFYKASIGKDTFVFPSEWGNQPFDFVSDSEKNIYIIYTDAGIWKIDPIALSAKKITADTYSGKDRQQIGQELTKLHPDAYLLWVSSVMISPDGKQVVYRTNRDSTRLDETSIWAIDLDSGKESQLVPPSVNNDILGFISDRDVVVGALADTRAIDVYDKSIIALDVPKVPNLRISAVQDGKIVISSHEEGSSTSTATVSSVDLSKGILTEISEISGYLDGEPRFSPSGTQVAIGYGDDPSVGVEDVMMVELSTKTQKLLSSSLQNKRSVKGNIIRFQWLNDETAVVETQTGSSFSSAVVNSTEK
>NZ_CP045802.1|WP_084137206.1|5546230_5547142_-|M23-family-metallopeptidase
MRYKKLTIMMLSFVLVTFIFPAGVFAADYSIVFGNTPPSIVNFNSPLSNSSSAGFAAVNSKWNQPRSSGTNPHNGADLQAALNTNVYAPYDGWATGITVTGSYDIDFLVDANNNNVKDDGDYHVRFYHMNSRETDGKKSQGALIGKSGNQGDVPPHLHFGVCSTSGGLKWLRNEVNYRHLSSSNWSSGKDLDAYSVVAWNSNIASFTAYIRNDGTKESFSEVRIYYRTSAGSWTDGGVMNKSGDVYSYNFTGKVSSGTSVQWMFRMLRSGVSQAAFGPAKFYQPDNNPNASSYAYSYFTNTVT
>NZ_CP045802.1|WP_028598849.1|5545621_5546161_-|hypothetical-protein
MNRFPKAPLPMLVTGMILTALTGCTNEAPAEMPPPSPRVSSVSTPTATVSPTEIPTLSPTPSAPVGEIRTFTFGRLKLEVTQVIETRTKQSSDGGVPWEYQQVVYGAGARVRVLDTGMSDASITEDGKSHPQFGISFEPDGRQEIDEKLESFEITPDMRGIFSLESSVFVLGFEAYQAS
>NZ_CP045802.1|WP_028598850.1|5543973_5545434_+|catalase
MNRLTTNQGVPIGDNQNSRTAGPNGPTLLEDYQLLEKLAHFDRERIPERVVHARGAGAHGVFRTAASMKRWTKAAFLQDAGTETPVFVRFSTVIHGQHSPETLRDPRGFAVKFYTTEGNYDFVGNNLPVFFIRDAMKFPDMVHSLKPDPSTNIQHPDRYWDFMSLTPESTNMLLHLFSDEGIPANYREMRGSGVHAFKWVNEHGNRVYTKLRWVPKQGVRNLSGDEASAIQAHDFNHATRDLQEAIKRGDFPEWDLFVQILDPADLDSFDFDPLDPTKDWFEEDIPYVHVGTMTLNRNPDNVFAETEQVGFNPGVVVPGIEPSEDKLLQGRLFSYSDTQRYRVGTNYLQLPINCPFAQVSNNQRDGTMQHGKPGGSVNYEPSRHKDAPQEDPAYAEPPAPLAAGAQAGRQKIAKTNDFGQAGQVWRRYSAAEQDAVIRNLSGDLAQAESSTQLRAVCNFYRADADLGKRLAGALGVDLTPYLQHLG
>NZ_CP045802.1|WP_028598842.1|5557330_5558254_+|proline-dehydrogenase
MDIGSELYRKTLLTISGNSLVEKLTLKYGGKLAAKFIASQELDGALQVIGDLNRKGIMVTLDHLGEGIRALSEASGYREEYIRLVRGIEQAGVNSNVSLKPTQMGLALDPEACYANIRAVVREAAASGNFVRIDMEDSPYTQATIDMVKRLHGEGLTNVGTVIQAYLRRTQADVRDLIQSGVNLRLVKGAYKEPAEVAYQKKSEVIDNFKAIIRMHLDQGVYTAIASHDDTIIRWVREYASANRIGQDKFEFQMLYGLRMNEQARLASEGYRVRCYVPYGKMWYPYYTRRLAEKPANLMMVLQNMFR
>NZ_CP045802.1|WP_101807558.1|5558481_5560443_+|PAS-domain-S-box-protein
MKLNLPRLIELPQTSYALAEWPEQPPDRPLFRQETDGSWSWLPEALASLPDRLAAALPASAFPASLRLDELPPLPDGCPWLLLLDEGGQPCGCVSATAALEELRQSFRRLRAGFEATLETVDSAITVINADSEVIAWTGEAERMFGIRREEIMGRPADAFFQKERLQVLRALTTGEVLQGAQHQPRPDMHAVIHARPIELGGERIGAVAAEQDITSQIRLNQQLFRMTAKMQHLERKVERLDPSGADPFSAIRGGSPAVRASVETARKLASAKAPVLLLGESGVGKELYARAMHDAGPGPETPFIAINCGAISPTLFESELFGYERGAFSGADPRGRKGKLDLAAGGTLLLDEVGEMPLELQVKLLRVLQEKTFYAVGGTTLRRADCRILAATNRDLLAMIADGRFREDLYYRLSVVTLDIPPLRERTGDVYELLPAFLSEFALLYGRFIEACPHEVVQRLAAYDWPGNIRELRGAAERLVLLATDGVIRLEHLPPRLLQNAARQSSGTGGKSARSAATPDRLGWAGTSEAAGGAAFGEQVFGGPASGSAASGGPAYGAVPGSAASSELSVDGAALGRPFSAGPAPGGAAHGYGNGSQPFPPARWPDSPEDYERERIRRLLEAERGNKKAVARQLGISRATLYNRMKKLGMPL
>NZ_CP045802.1|WP_101807557.1|5561068_5562697_-|cupin-domain-containing-protein
MRLILLSGGSGKRLWPLSNEIRSKLFLKLLPAPDGTLESMMQRLCRQLREEGLLEGAVIVTHRSQAEITRAHAGADVPIVEEPAKRGTFTAAALGAAYLAGPGRAPEDEAVCVLPVDLFVEADFLALLRRLPEALARGADLGMIGTEPTHPSAQYGYIVPIREPRPRRPKRRAAAGGRKFGGMTDAGAGAGAGERAARPDADAGADGAGVGKSAARPDADAGADGAGVGRSAARPDADAGGNGARAGRNAAPPGADAGADGAGAGWLPVGRFAEKPDPPAATRLIKQGGLWNSGVFVFRLGWLLGQLQARGYPSSLPELLRGYDEWSEKSFDQELAEKASRSLVLRYAGSWKDLGSWSTFLSQLGEAQLGPGAVSAGARNTHLINELGCPIHVIGISDAVVAASPDGILVASKEHSDRIKEALRELPGLPMQEEKRWGSCRTLEIDRLSGGGQVLTRRVAVHAGKCTSYHLHEGKEEVWTVLSGEGRFMLEDEIYPIGPGSVMRFPPGSRHGVKAVTELQCMQVEIGRVLDERDIERLLMSW
>NZ_CP045802.1|WP_101807556.1|5562693_5564040_-|glycosyltransferase-family-4-protein
MKPRGSGRAGHAAPGRGRSPQARRSGWSVDWRGPLGRAGGLGGASRSYVRALRGAGLPVNASAAMGQPAAGRLAPGTRRMLVYHYPPHTLDPDRARRAGYGRVVLNAVWETSRIPSQWRRTINRYDAVLVPSRHNVQAMKDSGVSVPVYRVPHGVDTRRFRPGRPKAALSGAEGRFVFLSVFSFQHRKNPEALLRAYAEEFSEKDSVLLVIKTSGWREAGGSAGAERAIRRYVASLRLSHRPAPIHIVAGHIGERRLLGLYASADAFVLPTRGEGVGMPFMEALASGVPVIAPRWGGQSDFLTDGNSFAVPYKLRKPAESMKGAGAISRRFGGLFAQEGQLWAEADLAGLKRQLRAASRDVALCRRKGRQGCQDMKSWSWEAAGRQLRQALERIGTQPPRGGAAASRESGEADPPGFVSAALRGQRRRAPRGSGSAPADAKERRTRRK
>NZ_CP045802.1|WP_028598840.1|5565404_5566637_+|peptidase-T
MKSELIRRFVAYAAVDTRSDDSSETCPSTPGQLVLARQLADELEAIGLTEVTLDANGYVMATLPATSAKAVPTIGFLAHMDTASDFTGTNVKPQLIESYDGGDIVLSAEPGITLSPREFPELAGYKGQTLLTTDGTTLLGADDKAGIAEIMTAMAYLAAHPEIPHGRIRVGFLPDEEIGRGPHRFDVAAFGADFAYTMDGGPLGELEYESFNAAEAVVTIQGKNVHPGYAKGKMLNAQSIGMALHGRLPAGEVPEFTEGYEGFFHLISFEGTVDRTRMRYIIRDFDRESFENRKSLLATIAEEFRQTYGAGSVTLELKDQYYNMREKIEPVMHIVELARQALEDCGVKPDIKPIRGGTDGSQLSYMGLPTPNLFAGGENFHGRYEYVSADTMVKAAEVILRIAALAEEQA
>NZ_CP045802.1|WP_028598839.1|5567393_5568587_+|glycosyltransferase-family-1-protein
MRLALFTDTFAPQMNGVARTLGRLTAHLERRGIEHLVFAPASPEEATTPPPAPEAPPLSLRPSPSVPFLLYPECRLALPNLLSIRQQLDRFRPDLLHLATPFNIGLCGLRYARRRGLPHAASYHTHFDRYLAYYGMAKAVPLYWRYIRWFHRSCGATFAPSRETLLALYRQGVGGLRLWTRGVDSELFHPAKRRAGLVRERFGIAPDERILLYVGRIAPEKDVATLAELLRRLPASREGRARWLIVGDGPALPELRAAAPDNAIFAGYREGEELAELYASADLFVFPSSTETFGNVALEAMASGLPVIGADAGGIRESVRHEATGLLCPPGDAAAFASAIERLTAAPELARRMGEQGRSHAVTRSWVSIFDELLEQYGEVIERSRHAEHAGRSYRTG
>NZ_CP045802.1|WP_153784525.1|5568710_5571749_-|MMPL-family-transporter
MRSFIQGAFRNKAAVWLCVVLVLAMGTASYLKLPMEFLPEADNPEVTVTTIGPGYDAASMEALVTKPMQEATAGIKGKTASFASSGDSYSQLNLSFDSSTDMKQARMDVERAIAAVPLPERVAPPYVIQLNTSMIPVSWVTLTFDDTVAEAKRAEAEKDILEAFQGIDGIGAAQLSGRPQPSVTVAPDPDKLAAKGLPLQALYGVLQGRTGSASVGESQLGGSAVNLNVASTLRDVETLRKLPVAPGVALGDVAQVEAKSEAGGISRLGGKDALVLTVTKAPGANAVAVGEGVEKAAERLNEEIPGAELKVLMSTSEQVVHSVNSMMKEVLLGALFATLVILVFMRNIRATLVTIVSIPLSLGLTLYLLDLSGVSLNILTLGGVAVAVGRLVDDSIVVIENIFRRLQKERFSIPLVVDATREVSTAITASTLTTVAVFLPMGLLRGSLQAFLLPFALTVTYSLLSSLLVALTVIPLLGAGLFKGVSLKEHGPSRRFQRFLDWNLRRKWLPLTAAVVLLAGSIGAYVAMPKGALDTSDASNLTVTLKFKADATQERMDADGEKLESYLRSLPEQEWVYMSAGGNAESAQYGGVASRTQISYMLGLKKGTDAEALVEQVKAKAGAPADAALEVQTSSLIGGGGGSQVYVDVTGPDAATASSAAAKVMAAIEPVRDVLKVESNEQERKTVYTLEVDPAKAKSAELAQQLQGMLNPVPIGMLAGEDGRQTPVVLQPALAPADAAELDALTVLTDAGPQPVSAVAKWVKEEKPAVYYLKDGKPYVRIAAEAEPSRLSVVGADIAKAVGGLKLPEGTHAYVGGASADMSQDFADLGMIALISIGIVYLIMVLTFKTLRTPLAILFTLPLAAIGAVLGLIVTQVTPDFTAMFGALMLIGIVVTNAIVLLDRVKQNEETMPIREALLEAAGTRMRPILMTAVATVCAMLPLVFGSAESGSIVSQSLAIVVIGGLIVATVLTLVIVPCIYELLFFRKAARQRREAAGAAPKREEAGEALAL
>NZ_CP045802.1|WP_028598837.1|5572021_5572930_-|LysR-family-transcriptional-regulator
MTLQQLRYIIEVAARGSMNEAARRLFISQPSLSKAVQELEQELQITIFRRTNKGIELSTEGTEFLAYARQVVEQADLLESRYRSARQAPQHFSVSTQHYAFAVNAFVRLVEQYGQEEYDLALRETKTHEIIEDVRLLRSEIGILYRNEFNAQVIQKLLASASLEFHSLFTAEPHVFISIRNPLARKARVTVEDLEPYPYLSFDQGEYNSFHFAEEILSTLSHPKSIRVSDRATLFNLLIGLNGYTISTGVLSKDLNGNEIIPVPLECDETIEVGWISQRQRALSRLGAAYVEELERAVRRED
>NZ_CP045802.1|WP_101807554.1|5573134_5575204_-|catalase
MSEQPKRHPNETAKTERLKDFTVDNDGQKLTTNTGLHVAEDEHSLKAGVRGPTLMEDFHFREKMTHFDHERIPERIVHARGAGAHGYFQAYEPLTELTEAGFLQDPSKQTPVFVRFSTVAGSRGSADTVRDVRGFAVKFYTEEGNFDLVGNNMPVFFIQDAMKFPDFIHAVKPEPHNEIPQAQSAHDTFWDFVVHNTETAHMVMWAMSDRSLPRSYAMMEGFGVHTFRLVNAEGKARFVKFHWKPLLGTHSLVWDEVQKLGGKDPDFNRRDLHDSIEAGRCPEWEFGIQVLEEEDEFKFGFDILDPTKLWPEELVPVRKIGKLTLNRNTDNYFAETEQIAFHPGHLVKGIDFSNDPLLQGRLFSYTDTQLSRLGGPNFNELPINRPMCPVHNNQRDGMHRMTINRGPAAYHKNGIAGGSPHPSADGYKHHQEKVEGHVTRERSDSFKDHYSQAALFWNSMSDVEKGHIVSAFSFELGHVKDKALRQAVVDMFANVSGELAAGIAANIGAASPAEADGAAGKSKSGASPALSMMNTVKTPKGRKVAVLVAGGFDGAATDALVRELRAAGIVPEFCSTRLGPIKSGSGADVEADHSFLTSDSVLFDAVLVAGGKASVEALAAEPKLADFLKEAFRHFKAIGFARTEDAERLLALAGIKAQAGDPGLLAGDGLGQPFIQAVAEHRHWTRQAQ
>NZ_CP045802.1|WP_153784526.1|5575286_5577047_-|HAMP-domain-containing-protein
MLKLRTVLSLGFAGVLLLTMVVGGAGWFQVGSVKGTYQQLMEERVGNIVLIQNLRYLAASEDKNIRGYLLTGQEKNYTAYNQDRKAFAAGMERLQADMREEKAAGLVTELHRLEGEYGKVVAELTKLRQRGDTEGYTALLVEKSIPLSAQLSDKAAELEAFQQSLLDESIAASQEQVERTRLVLAIIVAAALLVGAAAAAWLTRLIVRPVRATARLAGDIASGNLGGEDMERPRIAELGAMAESVNAMKAKLSRLIETIGDNADELGGAARLLARSSSSAEKDSERMVETMRLISESAEGQRQRMGENRTALEESSVSLNGVAESASLTAESSERAMQAAEAGKARMAEARRRMDSVGAAIEQAGAVAERLVRQAKEIGQVTDVITAVAEQTKLLSFNASIEAARAGEHGRGFAVVAQEVKKLSDETAASSVRIAAAVRGMAQQADEAAEAMVRGLEETKAGFRELERTGAAFDDVNESIAVVAEQAQEVSASTEELSASMEELLASSDDLLGLATSIAKHTVHAEELCAAQRGVMQEVSASTEQLRDMSDALRQELSGFRRAENAGSPPGRRDGAAAGGSSPDAA

Crispr_ID: NZ_CP045802_28

• CRISPR_ID: NZ_CP045802_28
• CRISPR_location: 5717235-5717504
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 4 spacers

Consensus repeat of NZ_CP045802_28

Consensus_repeat	Method
CTGCACCGCCGCCTCCAGTGGCGGTTACAGTGCCGCCATTGATGGTGACTGTGCCACCAGCA	PILER-CR
TGACCACCACCGATACCTGCACCGT	PILER-CR

spacers of NZ_CP045802_28

>28.1|5717297|37|NZ_CP045802|PILER-CR
TCGCCATCCAGACCACTACCGATACCTGCTGAATATT
>28.2|5717396|22|NZ_CP045802|PILER-CR
CCAGTGTAACCACCACCGATAC
>28.3|5717332|64|NZ_CP045802|PILER-CR
TGAATATTCTCCAGTGGCGGTTACAGTGCCGTCATTGATGGTGACTGTGCCACCAGCACCAGTG
>28.4|5717421|65|NZ_CP045802|PILER-CR
CGCCTCCATTGGCGGTTACAGTGCCGCCATTGATGGTGACTGTGCCACCATCCGTAACACCAGAT

CRISPR arrays and Neighbor proteins around NZ_CP045802_28

CRISPR arrays

The CRISPR arrays of NZ_CP045802_28

>merge|NZ_CP045802|28|5717235-5717504|PILER-CR,PILER-CR
CTGCACTGCCGCCTCCAGTGGCGGTTACAGCTCCGCCATTGATGGTGACTGTGCCACCAGCATCGCCATCCAGACCACTACCGATACCTGCTGAATATTCTCCAGTGGCGGTTACAGTGCCGTCATTGATGGTGACTGTGCCACCAGCACCAGTGTAACCACCACCGATACCTGCACCGTCGCCTCCATTGGCGGTTACAGTGCCGCCATTGATGGTGACTGTGCCACCATCCGTAACACCAGATTGACCACCACCGATACCTGCACCGT

>NZ_CP045802|28|5|5717235-5717464|PILER-CR
CTGCACTGCCGCCTCCAGTGGCGGTTACAGCTCCGCCATTGATGGTGACTGTGCCACCAGCA	TCGCCATCCAGACCACTACCGATACCTGCTGAATATT
	TTCTCCAGTGGCGGTTACAGTGCCGTCATTGATGGTGACTGTGCCACCAGCACCAGTGTAACCA
	CCACCGATACCTGCACCGTCGC
CTC	CATTGGCGGTTACAGTGCCGCCATTGATGGTGACTGTGCCACCATCCGTAACACCAGATTGACCA


>NZ_CP045802|28|6|5717307-5717504|PILER-CR
	TCGCCATCCAGACCACTACCGATACCTGCTGAATATT
	TTCTCCAGTGGCGGTTACAGTGCCGTCATTGATGGTGACTGTGCCACCAGCACCAGTGTAACCA
	CCACCGATACCTGCACCGTCGC
CTC	CATTGGCGGTTACAGTGCCGCCATTGATGGTGACTGTGCCACCATCCGTAACACCAGATTGACCA
CCACCGATACCTGCACCGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045802.1|WP_084136803.1|5723446_5724190_+|hypothetical-protein	unknown	unknown	gnl|CDD|373047
NZ_CP045802.1|WP_153784587.1|5726203_5727304_-|hypothetical-protein	unknown	unknown	gnl|CDD|293841
NZ_CP045802.1|WP_127464567.1|5729941_5730901_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028598055.1|5724251_5724560_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028600143.1|5708418_5708766_+|cupin-domain-containing-protein	unknown	unknown	gnl|CDD|380355
NZ_CP045802.1|WP_153784588.1|5727675_5729637_+|sensor-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_CP045802.1|WP_028598054.1|5724621_5724984_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224647
NZ_CP045802.1|WP_028600141.1|5710740_5711274_-|RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|224511
NZ_CP045802.1|WP_028598057.1|5722841_5723321_-|23S-rRNA-(pseudouridine(1915)-N(3))-methyltransferase-RlmH	unknown	unknown	gnl|CDD|376840
NZ_CP045802.1|WP_028598053.1|5725126_5725768_+|NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|225462
NZ_CP045802.1|WP_153784583.1|5704250_5704841_-|TetR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|182177
NZ_CP045802.1|WP_153784586.1|5718136_5722507_-|AAA-family-ATPase	unknown	unknown	gnl|CDD|226415
NZ_CP045802.1|WP_153784584.1|5704858_5705290_-|glyoxalase/bleomycin-resistance/extradiol-dioxygenase-family-protein	unknown	unknown	gnl|CDD|319947
NZ_CP045802.1|WP_028600142.1|5709721_5710744_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP045802.1|WP_028600146.1|5705431_5706343_-|copper-amine-oxidase-N-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|377924
NZ_CP045802.1|WP_043111058.1|5729625_5729868_-|NHLP-leader-peptide-family-natural-product-precursor	unknown	unknown	gnl|CDD|274786
NZ_CP045802.1|WP_028600140.1|5711910_5713485_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|223562
NZ_CP045802.1|WP_043111721.1|5707014_5708394_+|PLP-dependent-aminotransferase-family-protein	unknown	unknown	gnl|CDD|224089
NZ_CP045802.1|WP_153784582.1|5702880_5704239_+|MATE-family-efflux-transporter	unknown	unknown	gnl|CDD|240548
NZ_CP045802.1|WP_028600145.1|5706486_5706903_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379228

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP045802.1|WP_084136803.1|5723446_5724190_+|hypothetical-protein	gnl|CDD|373047	pfam14398, ATPgrasp_YheCD, YheC/D like ATP-grasp. A member of the ATP-grasp fold predicted to be involved in the modification/biosynthesis of spore-wall and capsular proteins.	4.36543e-51
NZ_CP045802.1|WP_153784587.1|5726203_5727304_-|hypothetical-protein	gnl|CDD|293841	cd16283, RomA-like_MBL-fold, Enterobacter cloacae RomA and related proteins; MBL-fold metallo hydrolase domain. Derepression of the romA-ramA locus results in a multidrug-resistance phenotype. 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. The class B metal beta-lactamases (MBLs) from which this fold was named are only a small fraction of the activities which are included in this superfamily. Activities carried out by superfamily members include class B beta-lactamases, hydroxyacylglutathione hydrolases, AHL (acyl homoserine lactone) lactonases, persulfide dioxygenases, flavodiiron proteins, cleavage and polyadenylation specificity factors such as the Int9 and Int11 subunits of Integrator, Sdsa1-like and AtsA-like arylsulfatases, 5'-exonucleases human SNM1A and yeast Pso2p, ribonuclease J and ribonuclease Z, cyclic nucleotide phosphodiesterases, insecticide hydrolases, and proteins required for natural transformation competence. Classical members of the superfamily are di-, or less commonly mono-, zinc-ion-dependent hydrolases, however the diversity of biological roles is reflected in variations in the active site metallo-chemistry.	1.52547e-65
NZ_CP045802.1|WP_028600143.1|5708418_5708766_+|cupin-domain-containing-protein	gnl|CDD|380355	cd02226, cupin_YdbB-like, Bacillus subtilis YdbB and related proteins, cupin domain. This family includes bacterial proteins homologous to YdbB, a Bacillus subtilis protein of unknown function. It also includes protein Nmb1881 From Neisseria meningitidis, also of unknown function. Proteins in this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold capable of homodimerization.	9.51668e-39
NZ_CP045802.1|WP_153784588.1|5727675_5729637_+|sensor-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.57605e-42
NZ_CP045802.1|WP_028598054.1|5724621_5724984_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	7.66146e-38
NZ_CP045802.1|WP_028600141.1|5710740_5711274_-|RNA-polymerase-sigma-factor	gnl|CDD|224511	COG1595, RpoE, DNA-directed RNA polymerase specialized sigma subunit, sigma24 homolog [Transcription].	2.90638e-37
NZ_CP045802.1|WP_028598053.1|5725126_5725768_+|NAD(P)-dependent-oxidoreductase	gnl|CDD|225462	COG2910, COG2910, Putative NADH-flavin reductase [General function prediction only].	6.34277e-89
NZ_CP045802.1|WP_153784583.1|5704250_5704841_-|TetR-family-transcriptional-regulator	gnl|CDD|182177	PRK09975, PRK09975, DNA-binding transcriptional regulator EnvR; Provisional.	2.00747e-12
NZ_CP045802.1|WP_153784586.1|5718136_5722507_-|AAA-family-ATPase	gnl|CDD|226415	COG3899, COG3899, Predicted ATPase [General function prediction only].	1.17892e-31
NZ_CP045802.1|WP_153784584.1|5704858_5705290_-|glyoxalase/bleomycin-resistance/extradiol-dioxygenase-family-protein	gnl|CDD|319947	cd08359, VOC_like, uncharacterized subfamily of vicinal oxygen chelate (VOC) family. 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.	2.92785e-49
NZ_CP045802.1|WP_028598057.1|5722841_5723321_-|23S-rRNA-(pseudouridine(1915)-N(3))-methyltransferase-RlmH	gnl|CDD|376840	pfam02590, SPOUT_MTase, Predicted SPOUT methyltransferase. This family of proteins are predicted to be SPOUT methyltransferases.	1.03847e-87
NZ_CP045802.1|WP_028600146.1|5705431_5706343_-|copper-amine-oxidase-N-terminal-domain-containing-protein	gnl|CDD|377924	pfam07833, Cu_amine_oxidN1, Copper amine oxidase N-terminal domain. Copper amine oxidases catalyze the oxidative deamination of primary amines to the corresponding aldehydes, while reducing molecular oxygen to hydrogen peroxide. These enzymes are dimers of identical subunits, each comprising four domains. The N-terminal domain, which is absent in some amine oxidases, consists of a five-stranded antiparallel beta sheet twisted around an alpha helix. The D1 domains from the two subunits comprise the 'stalk' of the mushroom-shaped dimer, and interact with each other but do not pack tightly against each other.	1.44465e-24
NZ_CP045802.1|WP_043111058.1|5729625_5729868_-|NHLP-leader-peptide-family-natural-product-precursor	gnl|CDD|274786	TIGR03793, TOMM_pelo, NHLP leader peptide domain. This model represents a domain that is conserved among a large number of putative ribosomal natural products (RNP) precursor, including the thiazole/oxazole-modified microcins (TOMMs). As a leader peptide domain, likely to be removed from the mature product, this domain is unusual in several ways. First, it is longer than most previously described RNP leader peptides. Second, most of the domain is homologous to nitrile hydratase alpha subunits. Finally, it appears that this domain correlates with a specific family of cleavage/export proteins while members undergo modifications by different classes of peptide maturase, including cyclodehydratases, lantibiotic synthases, radical SAM peptide maturases. This family is expanded especially in Pelotomaculum thermopropionicum SI. [Cellular processes, Biosynthesis of natural products].	5.41953e-12
NZ_CP045802.1|WP_028600140.1|5711910_5713485_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein	gnl|CDD|223562	COG0488, Uup, ATPase components of ABC transporters with duplicated ATPase domains [General function prediction only].	6.60685e-165
NZ_CP045802.1|WP_043111721.1|5707014_5708394_+|PLP-dependent-aminotransferase-family-protein	gnl|CDD|224089	COG1167, ARO8, Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs [Transcription / Amino acid transport and metabolism].	1.03166e-129
NZ_CP045802.1|WP_153784582.1|5702880_5704239_+|MATE-family-efflux-transporter	gnl|CDD|240548	cd13143, MATE_MepA_like, Subfamily of the multidrug and toxic compound extrusion (MATE)-like proteins similar to Streptococcus aureus MepA. The integral membrane proteins from the MATE family are involved in exporting metabolites across the cell membrane and are responsible for multidrug resistance (MDR) in many bacteria and animals. This subfamily includes Streptococcus aureus MepA and Vibrio vulnificus VmrA and functions most likely as a multidrug efflux pump.	1.33935e-103
NZ_CP045802.1|WP_028600145.1|5706486_5706903_-|GNAT-family-N-acetyltransferase	gnl|CDD|379228	pfam13508, Acetyltransf_7, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.737e-11

Protein sequences

>NZ_CP045802.1|WP_028600140.1|5711910_5713485_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein
MSVIRLENVTKKYEDSVIFRDIYFRVMQGERIGLIGRNGAGKSTVFKLIMGKEEPTSGRVEIDPKVKIGYFSQFSELSGSLSVQQELEMCFEQVACIERELQEVGEKLGMSPDDNETEELLARQAELFEQMDHLDGWNVSIEINTVLTKLGFNDRSRNQPIDELSGGWRNRAALAKMLIELPDVVLLDEPTNYLDIEGITWLEQWLYRFKGAMILVSHDRQFIDKVVTRTIEIENYHFQQYEGNYTEYVRKKKMRKKELDRQFEWEEQLLLLESEEIDNRASRKAASKDRLSRKLADNKKRIEPHPVNVLITDIYEKLRFPDKLCEVKKIGQTYEGRQIFENVSFDIQKEDRLVITGPNGSGKSTLIKVLTGTEKPESGEVIWEKGVSYAYFNRMWEELDPKDTVSHAVNTYGLGLDAPRKKVAKFLAMLQFSEADLSKAIGNLSGGQKARVALAKCLLSGAAVIVLDEPTNHLDLMSIQVMEQALIHFPGAVITVSHDRFFIDKIGTKMLTFDPAAGVTEQRL
>NZ_CP045802.1|WP_028600141.1|5710740_5711274_-|RNA-polymerase-sigma-factor
MEFQYLINTDSMSETELCRLMTTYGDDVRRYAYAITRNQEQAKDIAQEVFLKAFHHVGSFRGNSSFKTWLFAIARNLAINEMRSSYVRRIVLFEWVHPQANERSAESDYFAEQSVQELRGIILSLPAKLREALILTLEHELTMAEAASLMGVSEGTVKSRLHRARKIINKKWKEAER
>NZ_CP045802.1|WP_028600142.1|5709721_5710744_-|hypothetical-protein
MSEHSMEWEDKVKQGLFAEETFSEEMKRSVLDAVNRRHARYRLRPWKQLLGSAMLVAAALLVAIHWPSDPASKMAAGSPDSVSGPASGSPESAPLPVSFEPLAAKDWERGQPTYAEDPDILPGLSNKFNPLSNESNERIDQIPFSDIQLLEEKPIEGFGTALRYTLKPGSTAPHVLPNNGAYFGFTVDGSTEPDTLYHYGTGHMYDLKFSMTRLFGQEALKIEQTICRTDGESCVWYFRKDVHGEVYSLMRLDAASYERDWDGDGKEEAIVATHKRNQIYVFKEQDGRLLWTSIRDALRAGRDDEVQYDDGRGVFLLRSAGGMLETYRLQGEPDSLVRVG
>NZ_CP045802.1|WP_028600143.1|5708418_5708766_+|cupin-domain-containing-protein
MKTGQLEKINLLELTRGVSEYKNWMVSEVNDHALRIAVMNGPFHWHKHDEGDELFLVLEGELYIDLEGETVSLKPGESFTIPQGVMHRTWSKERTVNLCVEKTATVTSGLDTQQE
>NZ_CP045802.1|WP_043111721.1|5707014_5708394_+|PLP-dependent-aminotransferase-family-protein
MKYAKVRDGLKQQINSGAIKPGAKLPSIRELSLQWACSKNTVIRAVDELEKEHLIYSVPKSGHYVLVRSSPSDDPPQGRIDFAAAAPDPGLIPYEELQHGLNRAVQLYGDQLFAYGDPFGFPSLREALSRHLAAAQVFAGPERICVVSGSQQALHLLASMPFPNGKSTILVEQPCYAGMLKALDLLGATAIGIPRTESGLDLEEVERHFRSNSIRFFYTVPRYHNPLGTSLSRREKEALADLADRHDVYIVEDDYLADLETDRKSDPIFSYDRSGRVIYIRSFSKTMLPGLRLGAAVLPEAFVPMFRRYKSMSDLSTAALSQAALEIHLGSGLFQRHAAMVKDRYRSRMMALQEACGRHLSGGFRLSPSGGGIFACLELPEHPGAEELAAALRQKDVLVFPTTPCYLPGTGSSNSWRLSIIRTNEHQIEQGIRLIGQTADELASRGRPTGPGRSAIAWI
>NZ_CP045802.1|WP_028600145.1|5706486_5706903_-|GNAT-family-N-acetyltransferase
MEWIPGDLPYRMSDRTEELQPDVVVGLLQGSYWAADRSKETILDSWRDSLCFGVYGEDGVQVAFMRVVTDGATFAWLCDVIVVPEHRGKGLGKWMMSVLIGHPRLRGTAIHLGTRDAHGLYEQYGFERRETMVRRAVR
>NZ_CP045802.1|WP_028600146.1|5705431_5706343_-|copper-amine-oxidase-N-terminal-domain-containing-protein
MGKKRLLSSLIGVAMLAAMGNSAFAAEAPLHLNVNGTKLADQKPVIIDQSILVPIRTISQLPGFHVDWDNKSKTVSVTNGSTQDVLKLTVGKTKAVLGASTVTVSVPPRNIGSSVYVPLRFIAESLNAYAAWDAESRTAVVYPFPASEEYKSEDLAASRQAVLGLPKISLKDHLGFTPDVRTTTYYFPQNQSQKFFIQEGEYIRYFEVENGAAWQRWEGQAGAKKAGERDAVPNLVPAVKGEWGKRPAYSGAYVYFMHEWMAGEVRYGLLDETGEGTELGSKEGVFDQVIIFPIDGEKGMELR
>NZ_CP045802.1|WP_153784584.1|5704858_5705290_-|glyoxalase/bleomycin-resistance/extradiol-dioxygenase-family-protein
MKASSFYPVLLTDQVRSTASFYEEHFGFQKVFEADWYVSLKLSGEKVSYELAVLDAAHPTIPEPYRNRTNGLILNFEVEDVDAQYDRLIRDAGLPLALELRSEDFGQRHFITSDPNGVLIDVITVIPPSDGYSEQYSEQIWNE
>NZ_CP045802.1|WP_153784583.1|5704250_5704841_-|TetR-family-transcriptional-regulator
MKRSKEEAAETIRKLMEVARSHFAEHGYAEAALESIVQEAGLTRGAVYHHFRSKKDLFRAVLADVQQDVAERVESEAATSEEMGEQLYLGCRAFILAAIEERNRRILLIDGPAIVGWEAWREMDRHHSMRLLREQLGLMQEHGYVRPMPLDALVHFISGGLNETALWLAGASVEPDAQEETMKMLAFLLDGLKKQS
>NZ_CP045802.1|WP_153784582.1|5702880_5704239_+|MATE-family-efflux-transporter
MDAENLHYFEKAPIAKAVAHFAVPMMLGTSMSVIYSILNAYFLGTLHDTAMLTALALTLPLFAIIMALGNLIGMGSGTFISRLLGERSYDEAKQVSSFAFYSSLVLGLIVMAIGLPLIDPIVHSLGATPDSFGFTKDYVTVMLIGSPLVVLFFTLENIVRAEGAAVTSMAGMMLSVAVNIALDAIAVFVLDWGVVGVASATVVSNGVASAFYAYHIGVKSRFLTVSARWFKASRKILANVFKIGVPVFIMSVFLGAMSLILNHYLVEYGDPAVAAYGISSRLLQFPEFILMGLCEGVVPLIAFSFAANKGRMKQTIGFTIKTILALAASFGVIVYLVSDHLIGWFTHDPHLIEMGSYILHVTFLSLFITGLTTLFVGIFQATAQGTAAFIMSVIQGITLIPVLYFADRLHGFHGVVWSLVIADAAAFLVGAILLYALRKKLQPDLEGLVQGG
>NZ_CP045802.1|WP_153784586.1|5718136_5722507_-|AAA-family-ATPase
MRYPSMTTNDMKLKDYLIDVGSPVALPIFIPLSIAITELVYREHQQTAVIGYLNPANIRLESETPAKQVRLSAYMDWDEVYQSPEQTGLLNLQINGRSDLYSLGVIFYVMLTGTTPFQPEEGDSWAVAHIRMPPAAWTSSSDALQSIIMKLLAKSPDDRYQSAYGLLDDLRQCERMLVDDDKMHAFEIGRLDRLRSFRLPDALYGNHVAIERMQAALAQAASGASVFRWLCGSAGSGKSELVQKLREDIAAVGGRLVAGVGEQSRSVHPLEPLLQALRQWIDQLWSDPPETIARLQERLTAVFGQDAQTIVTVLPEARILFANLVDIQAKQRPTSDADSWVRFGRLLPALIRALVNYGSPRTHGRAVPEGNDQPVVLFIDQIQFADEHTLDAIQIMVRNRGIPGLFVIGAIRTEHVERVPWLADRLRTNPDEWVDLHPWTYEDIRQYVVDAVQEDSARVRLLARSLHLLTDGNPHALRLRLEDWVRDKKLVFDDTQRRWTWETEIARLTEDLQAKRERLEIDFAMLTDEAKGLLATAAAMGLTFRLTVLCACTDLQPDEVLRHFDAAEALGIVCWEDEPDLYSKSDRMYMFMHDHLHHLAYTYDAAGNAQRHLKIGQYLLRDYRNAMDSERLRTAVDHLNRGRAELSASERKQLASYNAQVGQQFGQERRFDKGQAYMEVGLELVDGDDEPLFYQLKRAAVEFAYMSGNTEQSKQHLLDMDQLGERLHRADRAWVWNKLLEMNSFVENETAINYGKQALEAYGWHLREKPSKLVVLREIIHTLGHMRSKQARRITLASPHDEDYMALCESVELIMFQLAMHDGNALIDLYARFIRYGLGKGLNASLLSIMCVYELLMQRGLKSRYTGANPLARLRTIGDAMDYDPKYQHTIDFTVGMFQQLDHPASAYLHMERALRGALEMDRVTVANVDMILCLVTYNHDLNALSNLLTYFDKDLKSYGASDTTLEMADIMRRYLVALRDVDALTPFVAIPSGLDDEDNVSYMCKLEVAYLSGQYREALHWAKRARENEFAMDWVRVWKHRLYETLALAAVYPEVDAVERKSIKRSMQRQLREMKRRKGYLGVDSSAYLLLNAEWARVTGDERGTWRGYTDAVQRAKEEQYALIEAIACERLAAYLQHHAKKPSAALIAAMDACTAYTLWGADAKVAQMRREYPNLQWMVTQPNEDVPAEEENRIDTASASTRTPRVYPYRSVDRRELERPDELLRQMMDWTSRSHGERSWLDHFLHIALRQAGADRGSIIRCRNDEFQLEASSDRQVHHEVSALAAMSVLRYTIMMNEAVMLHDATESHFLRDAYIREWRTKSILCLPIQVPGEDYLILLYLENRTVAGVFTERDVNVLQLLITRVVYLKMLADVSIEIAPISSDAEVLAEPLTKRELEILVAMAEGLSNQEIAERFAITERTVKKHGTSIFGKLDVKRRGQAVSRARALHIID
>NZ_CP045802.1|WP_028598057.1|5722841_5723321_-|23S-rRNA-(pseudouridine(1915)-N(3))-methyltransferase-RlmH
MQIQIVCVGKLKEKYWTGGVDEYAKRLGAYAKLDIRELPDEKTPDSMSPAEEDQVRAREGERILGALRDGAHVVALAIDGETWSSEQLAAHLDKQAVYGGGSVSFVIGGSLGLSPAILKRADKKLSFGRMTYPHQMMRVMLLEQIYRGFRINRGEPYHK
>NZ_CP045802.1|WP_084136803.1|5723446_5724190_+|hypothetical-protein
MKKAGMTVAVQKDKWEQYGVLRAGPPLDARLPETRLLEKDALSSMLQRHPSVVLKPRDGSFGTNIIFIQRTETGAYRMQHENNAITMSGTDKVLEWLWIESKGRGYIVQERIPLARIGRRPFDIRVMVQRQKAASSPWTVTGSYAKAATKGYLVTNVASRPLPLLRALKSARIEDRSLPAKIARAALEAAERLGERYPDLRQVGFDIGIDRERRIWIIEGNYQPALRPFRLLKDSTMLRRIHWYRNH
>NZ_CP045802.1|WP_028598055.1|5724251_5724560_-|hypothetical-protein
MGLREVQGYDPVQITNSTSFNAYGAVEYSSIFCSDDLYSVQRDETWRASGRGVCLLTRITATVRTPSGDIAAEPYTSSGTSYSRFAIIQVGENRFQVTRIVS
>NZ_CP045802.1|WP_028598054.1|5724621_5724984_-|helix-turn-helix-transcriptional-regulator
MARANFKGEIPEEKRELCLVSDALNVIAGKWKLIILWQLKETRRFGELQRLLPGISKSILTSQLRELERDGMVHREVYHEVPPKVEYSLTGMGRGFLPILDSMGEWRKKHAAGKGEDADS
>NZ_CP045802.1|WP_028598053.1|5725126_5725768_+|NAD(P)-dependent-oxidoreductase
MNIAIIGANGVSGSLILKEAVDRGHDVTAIVRDASKISAANVAVIEKDLFDLTGADLRPFDVVVSAFKAPIGQETLYLDSSVALAAALQDAPDTKLIVVGGAGSLFVDADSTSLLMDTPDFPDFVYPTAFNAGKQLEHLRQTDSLTWTYISPAAFFDPEGPRTGSYRKGKDHVIPNAQGDSYVSYADFAIAVLDEIEHPQHVNERFTVVSDKE
>NZ_CP045802.1|WP_153784587.1|5726203_5727304_-|hypothetical-protein
MGVWIGIAAALAAALTLAYLYIRPALGGKPSPESRERIRRSKQYRDGVFAYPLPTPMLSGWKDQVSILGEFLKGTPQAVPDRPLDVERYSPASAAERENAVRVTWFGHSAVLLELGDMTVFLDPMLGRAPSPVPMIGGQRFKGSSPVDLERLPRLDAVVLSHDHYDHLDYPTILRLKEKTGMFIVPLGVAAHLERWGVAREAIRECDWSEAVKLNGLTLTCAAARHFSGRGLLSRNSTLWCSWVIEGQGRRIFFSGDSGYGPHFREIGETYGPFDLTLMECGQYDRRWASIHMLPEETVQAHRDVRGSLLLPIHWGAFRLALHAWTDPVERLLRAASADGVAVCTPRIGETVTLGQGEPPATPWWR
>NZ_CP045802.1|WP_153784588.1|5727675_5729637_+|sensor-histidine-kinase
MRTLRLCLFPALAVLALLAGWLHWPSLLSAAEPGDVAASAAPAARSSLDRWQVLPIPADATPGTAPPADADWLDAELREPRVELPKDAQGIWIRLRVPATEQWHRPGLLAGRMYSRHVQVYERGVLLYESSRGFDFDQGRLLVPLDAKPQETVLDVRILNKGERAGFLTPPQLGEFDELDRTYIRKELPSLLLGVSLVFLAAIMFICSSFLSRRQRGFWISLCLIALSAGLLISAYSPLLYLYFPDAAQVFLACFELSLFTMFPALGYFVNEALERKSPPFQRFTRWQTYYSAFGVLCFVAYRLSDGQLHAFYDLVSVVAVGFLILVQMVWISILSIAHTFQGDRQARILSLGLLAFAVSSAIDLILFYGSGKSYVLFLWKLGIVALIFSLVVILARRVSSDYKTLVSYSKQLEQFNLSLERTEKLKIISDLAASVAHEVRNPLQVTRGFLQLLSKKEDPQSQDYITIAVSELDRAAEIITDFLTFAKPDLEMIVKIDLHELLEQLDLIMGPHAAMHGGRLVIISEEGLEIMGSPSKLKQALINLIKNSVEAFGQEGIIELTARAEGGEAVLRLKDNGEGMDEEQLAKLGVPYFSTKTKGTGLGTMVTMRIIEVMNGSIDFRSEKGKGTEVTIRFPLTGQIVSEMTDAISLPD
>NZ_CP045802.1|WP_043111058.1|5729625_5729868_-|NHLP-leader-peptide-family-natural-product-precursor
MTVAVESLRVQIIRKAWKDEIFKQQLLADPKKAIKEAFDYEVAADIQVTAVAETEKHFYLVLPPSPENVANGQGEVELVW
>NZ_CP045802.1|WP_127464567.1|5729941_5730901_-|hypothetical-protein
MSIEWNLEMARKEAAAIFADAREGASACPEPLRGVLRQLIDRADPSAREGGSNFIAYLLPAWTGEQAGLPPAVGRELAVGSVYMMLHYLLLDDVMDGDEIGLGPKEALAAGQLLHSLFLERYERAVPGSAELWSRYRAYAGEWAQAVSQEGRQRAEPQDAAALAAKSAPVKIGAAAVWLAAGRPERIADAEQATELALASLQLADDWADWRDDLAAGEERSNAFLTLVRRMLDQPEEQPLAERLVRRAVYQEDAVERLAELVRGHRRELSDRHEAPSGLAGFHRAVLAGIEADVMSIRQTADGLALNGGFFHYLSHLEN

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP045802_23	23.2|5217827|18|NZ_CP045802|CRT	5217827-5217844	18	NZ_CP045802.1	4540205-4540222	1	0.944
NZ_CP045802_23	23.3|5217878|18|NZ_CP045802|CRT	5217878-5217895	18	NZ_CP045802.1	4540205-4540222	1	0.944
NZ_CP045802_23	23.5|5217980|18|NZ_CP045802|CRT	5217980-5217997	18	NZ_CP045802.1	4529759-4529776	1	0.944
NZ_CP045802_19	19.9|4207825|23|NZ_CP045802|CRT	4207825-4207847	23	NZ_CP045802.1	2850548-2850570	2	0.913
NZ_CP045802_19	19.9|4207825|23|NZ_CP045802|CRT	4207825-4207847	23	NZ_CP045802.1	4476117-4476139	2	0.913
NZ_CP045802_28	28.2|5717396|22|NZ_CP045802|PILER-CR	5717396-5717417	22	NZ_CP045802.1	5716952-5716973	2	0.909

1. spacer 23.2|5217827|18|NZ_CP045802|CRT matches to position: 4540205-4540222, mismatch: 1, identity: 0.944

agcgcgctgctgggcttc	CRISPR spacer
agcgcgctgccgggcttc	Protospacer
**********.*******

2. spacer 23.3|5217878|18|NZ_CP045802|CRT matches to position: 4540205-4540222, mismatch: 1, identity: 0.944

agcgcgctgccgagcttc	CRISPR spacer
agcgcgctgccgggcttc	Protospacer
************.*****

3. spacer 23.5|5217980|18|NZ_CP045802|CRT matches to position: 4529759-4529776, mismatch: 1, identity: 0.944

cgcgggctgccgggcttc	CRISPR spacer
cgcgggctgccgcgcttc	Protospacer
************ *****

4. spacer 19.9|4207825|23|NZ_CP045802|CRT matches to position: 2850548-2850570, mismatch: 2, identity: 0.913

cgtcggttcggcacccgcttgcc	CRISPR spacer
cgccggttcggctcccgcttgcc	Protospacer
**.********* **********

5. spacer 19.9|4207825|23|NZ_CP045802|CRT matches to position: 4476117-4476139, mismatch: 2, identity: 0.913

cgtcggttcggcacccgcttgcc	CRISPR spacer
cgccggttcgccacccgcttgcc	Protospacer
**.******* ************

6. spacer 28.2|5717396|22|NZ_CP045802|PILER-CR matches to position: 5716952-5716973, mismatch: 2, identity: 0.909

ccagtgtaaccaccaccgatac	CRISPR spacer
ccattgtaaccactaccgatac	Protospacer
*** *********.********

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP045802_2	2.1|416977|22|NZ_CP045802|CRT	416977-416998	22	JQ015307	Pectobacterium phage phiTE, complete genome	117722-117743	2	0.909
NZ_CP045802_2	2.1|416977|22|NZ_CP045802|CRT	416977-416998	22	KY514263	Pectobacterium phage vB_PatM_CB7, complete genome	9368-9389	2	0.909
NZ_CP045802_2	2.4|417157|22|NZ_CP045802|CRT	417157-417178	22	MH744420	Streptomyces phage Kromp, complete genome	24244-24265	2	0.909
NZ_CP045802_2	2.6|417256|22|NZ_CP045802|CRT	417256-417277	22	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	4097421-4097442	2	0.909
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NC_014331	Bacillus cereus biovar anthracis str. CI plasmid pCI-XO1, complete sequence	127566-127593	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP022045	Bacillus anthracis strain FDAARGOS_341 plasmid unnamed1, complete sequence	64227-64254	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NC_007322	Bacillus anthracis str. 'Ames Ancestor' plasmid pXO1, complete sequence	127318-127345	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NC_012579	Bacillus anthracis str. CDC 684 plasmid pX01, complete sequence	127641-127668	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP015777	Bacillus anthracis strain Tangail-1 plasmid pXO1, complete sequence	127318-127345	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP018904	Bacillus anthracis strain Tyrol 4675 plasmid pXO1, complete sequence	127009-127036	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP023002	Bacillus anthracis strain 14RA5914 plasmid pX01, complete sequence	78679-78706	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_AP019732	Bacillus anthracis strain PCr plasmid PCr-pXO1	73153-73180	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_AP018444	Bacillus anthracis strain CZC5 plasmid pXO1, complete sequence	127240-127267	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP029324	Bacillus anthracis strain 17OD930 plasmid pXO1, complete sequence	96537-96564	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NC_012656	Bacillus anthracis str. A0248 plasmid pXO1, complete sequence	127582-127609	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NC_010934	Bacillus cereus strain G9241 plasmid pBCXO1, complete sequence	185429-185456	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP019589	Bacillus anthracis strain SPV842_15 plasmid pX01, complete sequence	127318-127345	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP010853	Bacillus anthracis strain A1144 plasmid pXO1, complete sequence	127300-127327	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP007665	Bacillus anthracis str. Vollum plasmid unnamed, complete sequence	74529-74556	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP008847	Bacillus anthracis strain HYU01 plasmid pX01, complete sequence	127563-127590	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP006743	Bacillus anthracis str. SVA11 plasmid pXO1, complete sequence	127475-127502	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_AP014834	Bacillus anthracis strain Shikan-NIID plasmid pXO1	127402-127429	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP029806	Bacillus anthracis strain London_499 plasmid pX01, complete sequence	126305-126332	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NC_001496	Bacillus anthracis virulence plasmid PX01, complete sequence	151889-151916	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NC_017726	Bacillus anthracis str. H9401 plasmid BAP1, complete sequence	127343-127370	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP014177	Bacillus anthracis strain Stendal plasmid pXO1, complete sequence	127318-127345	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP009597	Bacillus anthracis str. V770-NP-1R plasmid pXO1, complete sequence	100975-101002	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP009901	Bacillus anthracis strain 2002013094 plasmid pXO1, complete sequence	98473-98500	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP009340	Bacillus anthracis strain Ohio ACB plasmid 1, complete sequence	131365-131392	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP009696	Bacillus anthracis strain RA3 plasmid pXO1, complete sequence	69622-69649	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP009463	Bacillus anthracis strain SK-102 plasmid pXO1, complete sequence	115665-115692	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP009699	Bacillus anthracis strain BA1035 plasmid pXO1, complete sequence	78551-78578	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP009592	Bacillus cereus G9241 plasmid pBCX01, complete sequence	66799-66826	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP009543	Bacillus anthracis strain BA1015 plasmid pXO1, complete sequence	32187-32214	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP010321	Bacillus anthracis strain Canadian Bison isolate A0369 plasmid 1, complete sequence	13765-13792	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP009540	Bacillus anthracis str. Sterne plasmid pXO1, complete sequence	48110-48137	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP009330	Bacillus anthracis strain K3 plasmid 1, complete sequence	165158-165185	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP009324	Bacillus anthracis strain PAK-1 plasmid 1, complete sequence	72739-72766	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP009327	Bacillus anthracis strain Vollum 1B plasmid 1, complete sequence	171129-171156	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP001975	Bacillus anthracis str. A16R plasmid pXO1, complete sequence	127372-127399	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP009317	Bacillus cereus 03BB102 plasmid unnamed, complete sequence	16672-16699	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP009980	Bacillus anthracis strain Ames isolate BACI008 plasmid unnamed1, complete sequence	162097-162124	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP001971	Bacillus anthracis str. A16 plasmid pXO1, complete sequence	127403-127430	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NC_012473	Bacillus cereus 03BB102 plasmid p03BB102_179, complete sequence	120224-120251	5	0.821
NZ_CP045802_25	25.1|5386161|28|NZ_CP045802|CRISPRCasFinder	5386161-5386188	28	NZ_CP047132	Bacillus anthracis str. BF1 plasmid pXO1, complete sequence	95657-95684	5	0.821
NZ_CP045802_2	2.5|417202|31|NZ_CP045802|CRT	417202-417232	31	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	576349-576379	6	0.806
NZ_CP045802_24	24.1|5331237|34|NZ_CP045802|CRT	5331237-5331270	34	NZ_CP021025	Rhizobium sp. TAL182 plasmid pRetTAL182a, complete sequence	162867-162900	6	0.824
NZ_CP045802_24	24.1|5331237|34|NZ_CP045802|CRT	5331237-5331270	34	NZ_CP013512	Rhizobium sp. N1314 plasmid pRspN1314a, complete sequence	158812-158845	6	0.824
NZ_CP045802_2	2.5|417202|31|NZ_CP045802|CRT	417202-417232	31	NZ_CP015867	Streptomyces parvulus strain 2297 plasmid pSPA1, complete sequence	72297-72327	7	0.774
NZ_CP045802_2	2.5|417202|31|NZ_CP045802|CRT	417202-417232	31	NZ_CP015867	Streptomyces parvulus strain 2297 plasmid pSPA1, complete sequence	154088-154118	7	0.774
NZ_CP045802_2	2.5|417202|31|NZ_CP045802|CRT	417202-417232	31	NZ_CP020333	Martelella mediterranea DSM 17316 strain MACL11 plasmid pMM170, complete sequence	96124-96154	7	0.774
NZ_CP045802_6	6.3|921204|33|NZ_CP045802|CRT	921204-921236	33	NC_011366	Rhizobium leguminosarum bv. trifolii WSM2304 plasmid pRLG202, complete sequence	192599-192631	7	0.788
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NC_013354	Escherichia coli O103:H2 str. 12009 plasmid pO103, complete sequence	71226-71259	7	0.794
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP031909	Escherichia coli O103:H2 strain FWSEC0007 plasmid unnamed16, complete sequence	49814-49847	7	0.794
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP027389	Escherichia coli strain 2011C-4251 plasmid unnamed	44362-44395	7	0.794
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP014753	Escherichia coli strain PSUO103 plasmid, complete sequence	68676-68709	7	0.794
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	CP031285	Escherichia fergusonii strain 40A plasmid p46_40A, complete sequence	42488-42521	7	0.794
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP051657	Escherichia coli strain SJ7 plasmid pSJ7-1	338-371	7	0.794
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	CP043544	Escherichia coli strain F2_81 plasmid pF2_18C_FIB, complete sequence	69841-69874	7	0.794
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP024480	Escherichia coli strain 2011C-4315 plasmid unnamed1, complete sequence	23105-23138	7	0.794
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP022502	Salmonella enterica subsp. enterica serovar Kentucky str. SA20030505 plasmid unnamed2, complete sequence	5949-5982	7	0.794
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP022502	Salmonella enterica subsp. enterica serovar Kentucky str. SA20030505 plasmid unnamed2, complete sequence	53404-53437	7	0.794
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_AP014804	Escherichia coli O119:H6 strain EC404/03 plasmid pEC404/03-1, complete sequence	15735-15768	7	0.794
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP031163	Deinococcus wulumuqiensis strain NEB 479 plasmid pDrdI, complete sequence	356035-356069	7	0.8
NZ_CP045802_15	15.13|2513214|33|NZ_CP045802|CRISPRCasFinder,CRT	2513214-2513246	33	NC_003064	Agrobacterium fabrum str. C58 plasmid At, complete sequence	253996-254028	7	0.788
NZ_CP045802_17	17.1|3884698|30|NZ_CP045802|CRISPRCasFinder	3884698-3884727	30	NC_008271	Rhodococcus jostii RHA1 plasmid pRHL3, complete sequence	76141-76170	7	0.767
NZ_CP045802_24	24.1|5331237|34|NZ_CP045802|CRT	5331237-5331270	34	NZ_CP020948	Rhizobium sp. CIAT894 plasmid pRheCIAT894a, complete sequence	211754-211787	7	0.794
NZ_CP045802_24	24.1|5331237|34|NZ_CP045802|CRT	5331237-5331270	34	NZ_CP016293	Rhizobium leguminosarum strain Vaf10 plasmid unnamed5, complete sequence	261086-261119	7	0.794
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_CP028348	Novosphingobium sp. THN1 plasmid pTHN, complete sequence	814108-814141	7	0.794
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_CP029357	Azospirillum sp. CFH 70021 plasmid unnamed2	640909-640942	7	0.794
NZ_CP045802_2	2.5|417202|31|NZ_CP045802|CRT	417202-417232	31	MN586033	Corynebacterium phage EmiRose, complete genome	19245-19275	8	0.742
NZ_CP045802_2	2.5|417202|31|NZ_CP045802|CRT	417202-417232	31	AP021850	Deinococcus grandis ATCC 43672 plasmid: pDEGR-1 DNA, complete genome	283373-283403	8	0.742
NZ_CP045802_2	2.5|417202|31|NZ_CP045802|CRT	417202-417232	31	KC954774	Cronobacter phage CR8, complete genome	12079-12109	8	0.742
NZ_CP045802_2	2.5|417202|31|NZ_CP045802|CRT	417202-417232	31	NC_028672	Cronobacter phage PBES 02, complete genome	66256-66286	8	0.742
NZ_CP045802_2	2.5|417202|31|NZ_CP045802|CRT	417202-417232	31	NC_017974	Cronobacter phage CR3, complete genome	12077-12107	8	0.742
NZ_CP045802_2	2.5|417202|31|NZ_CP045802|CRT	417202-417232	31	CP042595	Streptomyces albogriseolus strain LBX-2 plasmid pSALBX2, complete sequence	21303-21333	8	0.742
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP038636	Cupriavidus oxalaticus strain X32 plasmid unnamed1, complete sequence	943017-943050	8	0.765
NZ_CP045802_15	15.19|2513609|34|NZ_CP045802|CRISPRCasFinder,CRT	2513609-2513642	34	NZ_CP039919	Agrobacterium tumefaciens strain CFBP6626 plasmid pAtCFBP6626b, complete sequence	134083-134116	8	0.765
NZ_CP045802_15	15.24|2513941|33|NZ_CP045802|CRISPRCasFinder,CRT	2513941-2513973	33	NZ_HG938354	Neorhizobium galegae bv. orientalis str. HAMBI 540 plasmid pHAMBI540a, complete sequence	1758627-1758659	8	0.758
NZ_CP045802_15	15.30|2514344|33|NZ_CP045802|CRISPRCasFinder,CRT	2514344-2514376	33	NC_014213	Meiothermus silvanus DSM 9946 plasmid pMESIL01, complete sequence	290210-290242	8	0.758
NZ_CP045802_17	17.1|3884698|30|NZ_CP045802|CRISPRCasFinder	3884698-3884727	30	NC_008042	Ruegeria sp. TM1040 plasmid unnamed, complete sequence	26198-26227	8	0.733
NZ_CP045802_18	18.1|4125593|34|NZ_CP045802|CRISPRCasFinder	4125593-4125626	34	NZ_CP015988	Sphingobium sp. EP60837 plasmid pEP1, complete sequence	108313-108346	8	0.765
NZ_CP045802_24	24.1|5331237|34|NZ_CP045802|CRT	5331237-5331270	34	NZ_CP022569	Rhizobium leguminosarum bv. viciae strain BIHB 1148 plasmid pSK05, complete sequence	123816-123849	8	0.765
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_CP015744	Shinella sp. HZN7 plasmid pShin-08, complete sequence	95925-95958	8	0.765
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_AP014705	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence	459794-459827	8	0.765
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_CP032325	Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence	77632-77665	8	0.765
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_LR536451	Methylocella tundrae isolate MTUNDRAET4 annotated genome plasmid 2	247330-247363	8	0.765
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_CP010410	Xanthomonas sacchari strain R1 plasmid unnamed, complete sequence	159115-159148	8	0.765
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_CP046574	Rhodococcus sp. WAY2 plasmid pRWAY02, complete sequence	263924-263957	8	0.765
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP031918	Escherichia coli O45:H2 strain FWSEC0003 plasmid unnamed12, complete sequence	28770-28803	9	0.735
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP012835	Salmonella enterica subsp. enterica serovar Cerro str. CFSAN001588 plasmid pCFSAN001588_002, complete sequence	19719-19752	9	0.735
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_LT900339	Gluconobacter oxydans 621H isolate WT-DSMZ plasmid 2	49356-49389	9	0.735
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NC_006672	Gluconobacter oxydans 621H plasmid pGOX1, complete sequence	49355-49388	9	0.735
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP016613	Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence	149004-149038	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP021449	Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence	1593490-1593524	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	CP023013	Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence	472973-473007	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP049790	Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence	1609242-1609276	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP049794	Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence	1062602-1062636	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP049788	Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence	1473610-1473644	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP022766	Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence	477208-477242	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP021763	Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence	527295-527329	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP015116	Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence	628425-628459	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP016555	Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence	130332-130366	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP049792	Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence	844078-844112	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052069	Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence	481021-481055	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP016915	Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence	182412-182446	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP016905	Ralstonia solanacearum strain KACC 10709 plasmid unnamed1	1473314-1473348	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP025986	Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence	707091-707125	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP022769	Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence	478470-478504	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP015851	Ralstonia solanacearum strain YC40-M plasmid, complete sequence	1702322-1702356	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP022773	Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence	489944-489978	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP022783	Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence	474401-474435	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP022791	Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence	371307-371341	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP022795	Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence	473492-473526	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052071	Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence	492223-492257	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP022482	Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence	603782-603816	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP009763	Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence	470494-470528	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	CP023015	Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence	474143-474177	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP022779	Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence	478487-478521	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052075	Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence	492223-492257	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052085	Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence	491730-491764	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052095	Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence	474193-474227	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052105	Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence	492223-492257	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052077	Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence	471510-471544	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052087	Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence	491730-491764	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052097	Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence	474193-474227	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052115	Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence	492223-492257	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052127	Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence	491730-491764	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052079	Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence	471513-471547	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052089	Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence	491734-491768	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052093	Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence	474193-474227	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052101	Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence	474193-474227	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052099	Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence	474193-474227	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052107	Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence	492223-492257	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP022781	Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence	1619404-1619438	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052117	Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence	492223-492257	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052125	Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence	471513-471547	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP022793	Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence	489925-489959	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP022785	Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence	489879-489913	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP022787	Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence	482089-482123	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP022756	Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence	481702-481736	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052129	Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence	472704-472738	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052121	Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence	492223-492257	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052123	Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence	471513-471547	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052131	Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence	491730-491764	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	CP011998	Ralstonia solanacearum strain YC45 plasmid, complete sequence	562482-562516	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052073	Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence	492222-492256	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052081	Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence	471513-471547	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052083	Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence	471513-471547	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052109	Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence	492223-492257	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052091	Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence	474195-474229	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052103	Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence	492223-492257	9	0.743
NZ_CP045802_6	6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921471-921505	35	NZ_CP052119	Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence	492223-492257	9	0.743
NZ_CP045802_15	15.10|2513017|34|NZ_CP045802|CRISPRCasFinder,CRT	2513017-2513050	34	MF417970	Uncultured Caudovirales phage clone 7S_1, partial genome	4092-4125	9	0.735
NZ_CP045802_15	15.10|2513017|34|NZ_CP045802|CRISPRCasFinder,CRT	2513017-2513050	34	AJ972879	Yersinia phage phiR1-37 complete genome	200078-200111	9	0.735
NZ_CP045802_15	15.10|2513017|34|NZ_CP045802|CRISPRCasFinder,CRT	2513017-2513050	34	NC_016163	Yersinia phage phiR1-37, complete genome	200078-200111	9	0.735
NZ_CP045802_15	15.18|2513543|34|NZ_CP045802|CRISPRCasFinder,CRT	2513543-2513576	34	NZ_CP042998	Aquisphaera giovannonii strain OJF2 plasmid pOJF2_1, complete sequence	74048-74081	9	0.735
NZ_CP045802_15	15.18|2513543|34|NZ_CP045802|CRISPRCasFinder,CRT	2513543-2513576	34	NZ_CP015739	Shinella sp. HZN7 plasmid pShin-03, complete sequence	357367-357400	9	0.735
NZ_CP045802_18	18.1|4125593|34|NZ_CP045802|CRISPRCasFinder	4125593-4125626	34	NZ_CP011600	Phytobacter ursingii strain CAV1151 plasmid pCAV1151-215, complete sequence	55888-55921	9	0.735
NZ_CP045802_18	18.1|4125593|34|NZ_CP045802|CRISPRCasFinder	4125593-4125626	34	NZ_CP011600	Phytobacter ursingii strain CAV1151 plasmid pCAV1151-215, complete sequence	57611-57644	9	0.735
NZ_CP045802_18	18.1|4125593|34|NZ_CP045802|CRISPRCasFinder	4125593-4125626	34	NZ_AP018757	Metakosakonia sp. MRY16-398 plasmid pMRY16-398_1, complete sequence	149424-149457	9	0.735
NZ_CP045802_18	18.1|4125593|34|NZ_CP045802|CRISPRCasFinder	4125593-4125626	34	NZ_CP051549	Phytobacter diazotrophicus strain UAEU22 plasmid unnamed1	94732-94765	9	0.735
NZ_CP045802_18	18.1|4125593|34|NZ_CP045802|CRISPRCasFinder	4125593-4125626	34	NZ_CP026198	Enterobacteriaceae bacterium ENNIH3 plasmid pKPC-c606, complete sequence	32886-32919	9	0.735
NZ_CP045802_18	18.1|4125593|34|NZ_CP045802|CRISPRCasFinder	4125593-4125626	34	NZ_CP026189	Enterobacteriaceae bacterium ENNIH2 plasmid pENT-812c, complete sequence	35838-35871	9	0.735
NZ_CP045802_24	24.3|5331368|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331368-5331401	34	NZ_CP039913	Agrobacterium tumefaciens strain CFBP6625 plasmid pAtCFBP6625b, complete sequence	347523-347556	9	0.735
NZ_CP045802_24	24.3|5331368|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331368-5331401	34	NZ_CP039905	Agrobacterium tumefaciens strain CFBP6623 plasmid pAtCFBP6623a, complete sequence	60045-60078	9	0.735
NZ_CP045802_24	24.3|5331368|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331368-5331401	34	NZ_CP039909	Agrobacterium tumefaciens strain CFBP6624 plasmid pAtCFBP6624, complete sequence	293633-293666	9	0.735
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_CP039965	Pseudorhodobacter sp. S12M18 plasmid unnamed1, complete sequence	1347715-1347748	9	0.735
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_CP025017	Rhizobium leguminosarum strain Norway plasmid pRLN5, complete sequence	227372-227405	9	0.735
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_CP054026	Rhizobium sp. JKLM12A2 plasmid pPR12A205, complete sequence	268367-268400	9	0.735
NZ_CP045802_24	24.11|5331900|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331900-5331933	34	NZ_LT969521	Pseudomonas aeruginosa isolate RW109 genome assembly, plasmid: RW109 plasmid 2	73206-73239	9	0.735
NZ_CP045802_24	24.11|5331900|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331900-5331933	34	NZ_CP032256	Pseudomonas aeruginosa strain AR_0111 plasmid unnamed, complete sequence	125366-125399	9	0.735
NZ_CP045802_24	24.11|5331900|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331900-5331933	34	NZ_CP034355	Pseudomonas aeruginosa strain IMP-13 plasmid pPYO_TB, complete sequence	122159-122192	9	0.735
NZ_CP045802_27	27.3|5556430|34|NZ_CP045802|CRT	5556430-5556463	34	NZ_CP053709	Acetobacteraceae bacterium strain PAMC 26569 plasmid unnamed1, complete sequence	436509-436542	9	0.735
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP025885	Escherichia coli strain 503440 plasmid p503440_68, complete sequence	5035-5068	10	0.706
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP027106	Escherichia coli strain RM14721 plasmid pRM14721, complete sequence	92447-92480	10	0.706
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP024583	Roseomonas sp. FDAARGOS_362 plasmid unnamed2, complete sequence	81844-81877	10	0.706
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP017185	Enterobacter roggenkampii strain DSM 16690 plasmid pDSMZ16690, complete sequence	27193-27226	10	0.706
NZ_CP045802_15	15.18|2513543|34|NZ_CP045802|CRISPRCasFinder,CRT	2513543-2513576	34	NZ_CP033971	Cupriavidus pauculus strain FDAARGOS_614 plasmid unnamed2, complete sequence	184683-184716	10	0.706
NZ_CP045802_15	15.18|2513543|34|NZ_CP045802|CRISPRCasFinder,CRT	2513543-2513576	34	NZ_CP038636	Cupriavidus oxalaticus strain X32 plasmid unnamed1, complete sequence	202928-202961	10	0.706
NZ_CP045802_15	15.18|2513543|34|NZ_CP045802|CRISPRCasFinder,CRT	2513543-2513576	34	NZ_CP043441	Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence	146160-146193	10	0.706
NZ_CP045802_18	18.1|4125593|34|NZ_CP045802|CRISPRCasFinder	4125593-4125626	34	NZ_CP042572	Enterobacter hormaechei strain E5 plasmid pE5_001, complete sequence	143519-143552	10	0.706
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_CP024310	Sinorhizobium fredii strain NXT3 plasmid pSfreNXT3c, complete sequence	363157-363190	10	0.706
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_CP023064	Sinorhizobium sp. CCBAU 05631 plasmid pSS05631b, complete sequence	213912-213945	10	0.706
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NC_016623	Azospirillum lipoferum 4B plasmid AZO_p3, complete sequence	180606-180639	10	0.706
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_CP013054	Sinorhizobium americanum CCGM7 plasmid C, complete sequence	385586-385619	10	0.706
NZ_CP045802_24	24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331502-5331535	34	NZ_CP013110	Sinorhizobium americanum strain CFNEI 73 plasmid C, complete sequence	2081844-2081877	10	0.706
NZ_CP045802_24	24.11|5331900|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	5331900-5331933	34	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	468293-468326	10	0.706
NZ_CP045802_28	28.1|5717297|37|NZ_CP045802|PILER-CR	5717297-5717333	37	NC_041875	Arthrobacter phage Jasmine, complete genome	28276-28312	10	0.73
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP025922	Escherichia coli strain 103605 plasmid p103605_83, complete sequence	39077-39110	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP025912	Escherichia coli strain 204446 plasmid p204446_92, complete sequence	46569-46602	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP047309	Citrobacter freundii strain L75 plasmid pCf76, complete sequence	63636-63669	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP017473	Enterobacter cloacae strain M12X01451 plasmid pM12X01451, complete sequence	98112-98145	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP023348	Escherichia coli strain ETEC-2265 plasmid unnamed2, complete sequence	13524-13557	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP019187	Salmonella enterica subsp. enterica serovar Pomona str. ATCC 10729 plasmid pATCC10729_01, complete sequence	25862-25895	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_KT754161	Shigella dysenteriae 1 strain CAR10 plasmid pCAR10, complete sequence	26566-26599	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	CP042948	Escherichia coli strain 90-9133 plasmid p90-9133_1, complete sequence	57631-57664	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP017848	Escherichia coli strain FMU073332 plasmid pEcoFMU07332d sequence	109957-109990	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP019175	Salmonella enterica subsp. enterica serovar Give strain CFSAN024229 plasmid pCFSAN024229, complete sequence	25544-25577	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NC_009787	Escherichia coli O139:H28 str. E24377A plasmid pETEC_35, complete sequence	6397-6430	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NC_009790	Escherichia coli O139:H28 str. E24377A plasmid pETEC_74, complete sequence	69661-69694	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP024244	Escherichia coli O128:H27 strain 90-9281 plasmid unnamed, complete sequence	57003-57036	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	MH450052	Escherichia coli plasmid pHN32wt, complete sequence	7704-7737	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	MH450053	Escherichia coli plasmid pHN32_1, complete sequence	7703-7736	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP027332	Escherichia coli strain 2013C-3277 plasmid unnamed1	18478-18511	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP041420	Escherichia coli strain STEC711 plasmid pSTEC711_4, complete sequence	47695-47728	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP038299	Escherichia coli O157:H7 strain TB182A plasmid pTB182A-5, complete sequence	50415-50448	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP053580	Salmonella enterica strain 94-0093 plasmid unnamed, complete sequence	7505-7538	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NC_022333	Escherichia coli plasmid pCss165Kan DNA, complete genome, strain: 4266 delta cssB::Km	10975-11008	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP029998	Salmonella enterica subsp. salamae strain SA20053897 plasmid pSA20053897.3, complete sequence	51451-51484	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP030210	Salmonella enterica strain SA20044414 plasmid pSA20044414.1, complete sequence	82511-82544	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP042531	Klebsiella aerogenes strain C9 plasmid pC9_001, complete sequence	128365-128398	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP022913	Escherichia coli O6:H16 strain 2011EL-1370-2 plasmid unnamed1, complete sequence	47288-47321	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP022156	Escherichia coli strain ABWA45 plasmid pABWA45_2, complete sequence	104231-104264	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP050381	Klebsiella pneumoniae strain 51015 plasmid p51015_OXA_244, complete sequence	68536-68569	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	CP025909	Escherichia coli strain 204576 plasmid p204576_83, complete sequence	77460-77493	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	CP025898	Escherichia coli strain 500465 plasmid p500465_79, complete sequence	70651-70684	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP046347	Citrobacter portucalensis strain FDAARGOS_738 plasmid unnamed1, complete sequence	115274-115307	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP024674	Citrobacter freundii strain UMH19 plasmid pUMH19, complete sequence	7825-7858	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP029982	Escherichia coli strain 99-3165 plasmid unnamed3, complete sequence	40562-40595	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP030780	Escherichia albertii strain 05-3106 plasmid unnamed2, complete sequence	25665-25698	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP011595	Klebsiella oxytoca strain CAV1099 plasmid pKPC_CAV1099, complete sequence	7239-7272	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP024250	Escherichia coli O182:H21 strain D181 plasmid unnamed2, complete sequence	49333-49366	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP054617	Azospirillum oryzae strain KACC 14407 plasmid unnamed3, complete sequence	13628-13661	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	CP049614	Escherichia coli O157:H7 strain K1516 plasmid pK1516-2	10555-10588	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP054717	Salmonella enterica strain 85-0120 plasmid unnamed1, complete sequence	214-247	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP020338	Shigella flexneri 4c strain 1602 plasmid unnamed2, complete sequence	75168-75201	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP044100	Citrobacter werkmanii strain FDAARGOS_616 plasmid unnamed1, complete sequence	1657-1690	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_LT985275	Escherichia coli strain R71 plasmid RCS70_p, complete sequence	36226-36259	11	0.676
NZ_CP045802_6	6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder	921404-921437	34	NZ_CP025918	Escherichia coli strain 120899 plasmid p120899_76, complete sequence	65091-65124	11	0.676
NZ_CP045802_15	15.13|2513214|33|NZ_CP045802|CRISPRCasFinder,CRT	2513214-2513246	33	NZ_CP039644	Azospirillum sp. TSA2s plasmid p2, complete sequence	226959-226991	11	0.667
NZ_CP045802_15	15.17|2513479|32|NZ_CP045802|CRISPRCasFinder,CRT	2513479-2513510	32	NZ_CP053347	Sphingomonas sp. AP4-R1 plasmid unnamed1, complete sequence	4911-4942	11	0.656
NZ_CP045802_15	15.17|2513479|32|NZ_CP045802|CRISPRCasFinder,CRT	2513479-2513510	32	AB624551	Enterobacteria phage FI genomic RNA, RNA-directed RNA polymerase beta chain region, isolate: 110112RS393	447-478	11	0.656

1. spacer 2.1|416977|22|NZ_CP045802|CRT matches to JQ015307 (Pectobacterium phage phiTE, complete genome) position: , mismatch: 2, identity: 0.909

agacaaaggggacaaaggggac	CRISPR spacer
cgacaaaggggacaaaggcgac	Protospacer
 ***************** ***

2. spacer 2.1|416977|22|NZ_CP045802|CRT matches to KY514263 (Pectobacterium phage vB_PatM_CB7, complete genome) position: , mismatch: 2, identity: 0.909

agacaaaggggacaaaggggac	CRISPR spacer
cgacaaaggggacaaaggcgac	Protospacer
 ***************** ***

3. spacer 2.4|417157|22|NZ_CP045802|CRT matches to MH744420 (Streptomyces phage Kromp, complete genome) position: , mismatch: 2, identity: 0.909

tccggcgggtccgcagggcgaa	CRISPR spacer
tccggcgggtccgcagggtgag	Protospacer
******************.**.

4. spacer 2.6|417256|22|NZ_CP045802|CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 2, identity: 0.909

cgcaacgggtccggcgggcccg	CRISPR spacer
ggcaacgggtacggcgggcccg	Protospacer
 ********* ***********

5. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NC_014331 (Bacillus cereus biovar anthracis str. CI plasmid pCI-XO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

6. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP022045 (Bacillus anthracis strain FDAARGOS_341 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

7. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NC_007322 (Bacillus anthracis str. 'Ames Ancestor' plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

8. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NC_012579 (Bacillus anthracis str. CDC 684 plasmid pX01, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

9. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP015777 (Bacillus anthracis strain Tangail-1 plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

10. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP018904 (Bacillus anthracis strain Tyrol 4675 plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

11. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP023002 (Bacillus anthracis strain 14RA5914 plasmid pX01, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

12. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_AP019732 (Bacillus anthracis strain PCr plasmid PCr-pXO1) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

13. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_AP018444 (Bacillus anthracis strain CZC5 plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

14. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP029324 (Bacillus anthracis strain 17OD930 plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

15. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NC_012656 (Bacillus anthracis str. A0248 plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

16. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NC_010934 (Bacillus cereus strain G9241 plasmid pBCXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

17. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP019589 (Bacillus anthracis strain SPV842_15 plasmid pX01, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

18. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP010853 (Bacillus anthracis strain A1144 plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

19. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP007665 (Bacillus anthracis str. Vollum plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

20. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP008847 (Bacillus anthracis strain HYU01 plasmid pX01, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

21. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP006743 (Bacillus anthracis str. SVA11 plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

22. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_AP014834 (Bacillus anthracis strain Shikan-NIID plasmid pXO1) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

23. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP029806 (Bacillus anthracis strain London_499 plasmid pX01, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

24. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NC_001496 (Bacillus anthracis virulence plasmid PX01, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

25. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NC_017726 (Bacillus anthracis str. H9401 plasmid BAP1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

26. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP014177 (Bacillus anthracis strain Stendal plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

27. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP009597 (Bacillus anthracis str. V770-NP-1R plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

28. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP009901 (Bacillus anthracis strain 2002013094 plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

29. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP009340 (Bacillus anthracis strain Ohio ACB plasmid 1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

30. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP009696 (Bacillus anthracis strain RA3 plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

31. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP009463 (Bacillus anthracis strain SK-102 plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

32. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP009699 (Bacillus anthracis strain BA1035 plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

33. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP009592 (Bacillus cereus G9241 plasmid pBCX01, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

34. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP009543 (Bacillus anthracis strain BA1015 plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

35. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP010321 (Bacillus anthracis strain Canadian Bison isolate A0369 plasmid 1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

36. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP009540 (Bacillus anthracis str. Sterne plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

37. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP009330 (Bacillus anthracis strain K3 plasmid 1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

38. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP009324 (Bacillus anthracis strain PAK-1 plasmid 1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

39. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP009327 (Bacillus anthracis strain Vollum 1B plasmid 1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

40. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP001975 (Bacillus anthracis str. A16R plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

41. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP009317 (Bacillus cereus 03BB102 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

42. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP009980 (Bacillus anthracis strain Ames isolate BACI008 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

43. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP001971 (Bacillus anthracis str. A16 plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

44. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NC_012473 (Bacillus cereus 03BB102 plasmid p03BB102_179, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

45. spacer 25.1|5386161|28|NZ_CP045802|CRISPRCasFinder matches to NZ_CP047132 (Bacillus anthracis str. BF1 plasmid pXO1, complete sequence) position: , mismatch: 5, identity: 0.821

tggta-catttaccatatacgcgccccat	CRISPR spacer
-aatacccttttccatatacgcgccccat	Protospacer
 ..** * *** *****************

46. spacer 2.5|417202|31|NZ_CP045802|CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 6, identity: 0.806

agcgcaaggcccggcgggtccggcaggagct	CRISPR spacer
tgcggctggcccggcgggtctggcaggagcg	Protospacer
 ***   *************.********* 

47. spacer 24.1|5331237|34|NZ_CP045802|CRT matches to NZ_CP021025 (Rhizobium sp. TAL182 plasmid pRetTAL182a, complete sequence) position: , mismatch: 6, identity: 0.824

acggcggagcagatggcagagacgcgcgaatcgc	CRISPR spacer
acggcggagcagatggaagagatgcgcggcttcc	Protospacer
**************** *****.*****. *. *

48. spacer 24.1|5331237|34|NZ_CP045802|CRT matches to NZ_CP013512 (Rhizobium sp. N1314 plasmid pRspN1314a, complete sequence) position: , mismatch: 6, identity: 0.824

acggcggagcagatggcagagacgcgcgaatcgc	CRISPR spacer
acggcggagcagatggaagagatgcgcggcttcc	Protospacer
**************** *****.*****. *. *

49. spacer 2.5|417202|31|NZ_CP045802|CRT matches to NZ_CP015867 (Streptomyces parvulus strain 2297 plasmid pSPA1, complete sequence) position: , mismatch: 7, identity: 0.774

agcgcaaggcccggcgggtccggcaggagct	CRISPR spacer
ggatcaaggcccggcggatgcggcaggactt	Protospacer
.*  *************.* ******** .*

50. spacer 2.5|417202|31|NZ_CP045802|CRT matches to NZ_CP015867 (Streptomyces parvulus strain 2297 plasmid pSPA1, complete sequence) position: , mismatch: 7, identity: 0.774

agcgcaaggcccggcgggtccggcaggagct	CRISPR spacer
ggatcaaggcccggcggatgcggcaggattt	Protospacer
.*  *************.* ******** .*

51. spacer 2.5|417202|31|NZ_CP045802|CRT matches to NZ_CP020333 (Martelella mediterranea DSM 17316 strain MACL11 plasmid pMM170, complete sequence) position: , mismatch: 7, identity: 0.774

agcgcaaggcccggcgggtccggcag---gagct	CRISPR spacer
ggcgcaaggcccggctgatccggccgtccga---	Protospacer
.************** *.****** *   **   

52. spacer 6.3|921204|33|NZ_CP045802|CRT matches to NC_011366 (Rhizobium leguminosarum bv. trifolii WSM2304 plasmid pRLG202, complete sequence) position: , mismatch: 7, identity: 0.788

cgcgccgacgatgatccatttcttcttgccgct	CRISPR spacer
cgccgcagcgacgatcaatttcttcttgccgcg	Protospacer
***  *..***.**** *************** 

53. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NC_013354 (Escherichia coli O103:H2 str. 12009 plasmid pO103, complete sequence) position: , mismatch: 7, identity: 0.794

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
cctgctggttcagcgtcagcagcaggtctgcgct	Protospacer
* .* * *************.******* *** *

54. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP031909 (Escherichia coli O103:H2 strain FWSEC0007 plasmid unnamed16, complete sequence) position: , mismatch: 7, identity: 0.794

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
cctgctggttcagcgtcagcagcaggtctgcgct	Protospacer
* .* * *************.******* *** *

55. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP027389 (Escherichia coli strain 2011C-4251 plasmid unnamed) position: , mismatch: 7, identity: 0.794

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
cctgctggttcagcgtcagcagcaggtctgcgct	Protospacer
* .* * *************.******* *** *

56. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP014753 (Escherichia coli strain PSUO103 plasmid, complete sequence) position: , mismatch: 7, identity: 0.794

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
cctgctggttcagcgtcagcagcaggtctgcgct	Protospacer
* .* * *************.******* *** *

57. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to CP031285 (Escherichia fergusonii strain 40A plasmid p46_40A, complete sequence) position: , mismatch: 7, identity: 0.794

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
cctgctggttcagcgtcagcagcaggtctgcgct	Protospacer
* .* * *************.******* *** *

58. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP051657 (Escherichia coli strain SJ7 plasmid pSJ7-1) position: , mismatch: 7, identity: 0.794

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
cctgctggttcagcgtcagcagcaggtctgcgct	Protospacer
* .* * *************.******* *** *

59. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to CP043544 (Escherichia coli strain F2_81 plasmid pF2_18C_FIB, complete sequence) position: , mismatch: 7, identity: 0.794

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
cctgctggttcagcgtcagcagcaggtctgcgct	Protospacer
* .* * *************.******* *** *

60. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP024480 (Escherichia coli strain 2011C-4315 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.794

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
cctgctggttcagcgtcagcagcaggtctgcgct	Protospacer
* .* * *************.******* *** *

61. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022502 (Salmonella enterica subsp. enterica serovar Kentucky str. SA20030505 plasmid unnamed2, complete sequence) position: , mismatch: 7, identity: 0.794

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
cctgctggttcagcgtcagcagcaggtctgcgct	Protospacer
* .* * *************.******* *** *

62. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022502 (Salmonella enterica subsp. enterica serovar Kentucky str. SA20030505 plasmid unnamed2, complete sequence) position: , mismatch: 7, identity: 0.794

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
cctgctggttcagcgtcagcagcaggtctgcgct	Protospacer
* .* * *************.******* *** *

63. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_AP014804 (Escherichia coli O119:H6 strain EC404/03 plasmid pEC404/03-1, complete sequence) position: , mismatch: 7, identity: 0.794

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
cctgctggttcagcgtcagcagcaggtctgcgct	Protospacer
* .* * *************.******* *** *

64. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP031163 (Deinococcus wulumuqiensis strain NEB 479 plasmid pDrdI, complete sequence) position: , mismatch: 7, identity: 0.8

ggggtctggggctgcggctcgctggtgc-tgctcgg	CRISPR spacer
gtggtctgggcctgctgctcgctggtgcgtacatg-	Protospacer
* ******** **** ************ *.* .* 

65. spacer 15.13|2513214|33|NZ_CP045802|CRISPRCasFinder,CRT matches to NC_003064 (Agrobacterium fabrum str. C58 plasmid At, complete sequence) position: , mismatch: 7, identity: 0.788

tcatatatgcaaatgatggaagctgtgcatgca	CRISPR spacer
atcgatacgcaaatgatggaagttgtgcatgcg	Protospacer
 .  ***.**************.*********.

66. spacer 17.1|3884698|30|NZ_CP045802|CRISPRCasFinder matches to NC_008271 (Rhodococcus jostii RHA1 plasmid pRHL3, complete sequence) position: , mismatch: 7, identity: 0.767

ggcgccatttccgccgcagagcctgcacgt	CRISPR spacer
tgcgccgtatccgccgcagagcctcccgga	Protospacer
 *****.* *************** *  * 

67. spacer 24.1|5331237|34|NZ_CP045802|CRT matches to NZ_CP020948 (Rhizobium sp. CIAT894 plasmid pRheCIAT894a, complete sequence) position: , mismatch: 7, identity: 0.794

acggcggagcagatggcagagacgcgcgaatcgc	CRISPR spacer
acggcggagcagatgggagagatgcgcaccttcc	Protospacer
**************** *****.****.  *. *

68. spacer 24.1|5331237|34|NZ_CP045802|CRT matches to NZ_CP016293 (Rhizobium leguminosarum strain Vaf10 plasmid unnamed5, complete sequence) position: , mismatch: 7, identity: 0.794

acggcggagcagatggcagagacgcgcgaatcgc	CRISPR spacer
acggcggagcagatggaagagatgcgcagcttcc	Protospacer
**************** *****.****.. *. *

69. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP028348 (Novosphingobium sp. THN1 plasmid pTHN, complete sequence) position: , mismatch: 7, identity: 0.794

tcagcgtatcgccgatctcgccgccttcgcggag	CRISPR spacer
acagcgtctcgccgatctcggcgccttggacgcg	Protospacer
 ****** ************ ****** *  * *

70. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP029357 (Azospirillum sp. CFH 70021 plasmid unnamed2) position: , mismatch: 7, identity: 0.794

tcagcgtat-cgccgatctcgccgccttcgcggag	CRISPR spacer
-cggcgcctgcgccgacctcgccgccttcgccgaa	Protospacer
 *.***. * ******.************** **.

71. spacer 2.5|417202|31|NZ_CP045802|CRT matches to MN586033 (Corynebacterium phage EmiRose, complete genome) position: , mismatch: 8, identity: 0.742

agcgcaaggcccggcgggtccggcaggagct	CRISPR spacer
tattcaaggcccggcggggccagcaggagag	Protospacer
 .. ************** **.*******  

72. spacer 2.5|417202|31|NZ_CP045802|CRT matches to AP021850 (Deinococcus grandis ATCC 43672 plasmid: pDEGR-1 DNA, complete genome) position: , mismatch: 8, identity: 0.742

agcgcaaggcccggcgggtccggcaggagct	CRISPR spacer
tgggcgaggaccggcgggtccggcaggcctg	Protospacer
 * **.*** *****************  . 

73. spacer 2.5|417202|31|NZ_CP045802|CRT matches to KC954774 (Cronobacter phage CR8, complete genome) position: , mismatch: 8, identity: 0.742

agcgcaaggcccggcgggtccggcaggagct	CRISPR spacer
tccttgtggtccggcgggtccggcaggacct	Protospacer
  * .. **.****************** **

74. spacer 2.5|417202|31|NZ_CP045802|CRT matches to NC_028672 (Cronobacter phage PBES 02, complete genome) position: , mismatch: 8, identity: 0.742

agcgcaaggcccggcgggtccggcaggagct	CRISPR spacer
tccttgtggtccggcgggtccggcaggacct	Protospacer
  * .. **.****************** **

75. spacer 2.5|417202|31|NZ_CP045802|CRT matches to NC_017974 (Cronobacter phage CR3, complete genome) position: , mismatch: 8, identity: 0.742

agcgcaaggcccggcgggtccggcaggagct	CRISPR spacer
tccttgtggtccggcgggtccggcaggacct	Protospacer
  * .. **.****************** **

76. spacer 2.5|417202|31|NZ_CP045802|CRT matches to CP042595 (Streptomyces albogriseolus strain LBX-2 plasmid pSALBX2, complete sequence) position: , mismatch: 8, identity: 0.742

agcgcaaggcccggcgggtccggcaggagct	CRISPR spacer
gcatcaaggcccggcggatgcggcaggactt	Protospacer
.   *************.* ******** .*

77. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP038636 (Cupriavidus oxalaticus strain X32 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.765

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tgttgtcagacagcgtcagcgtcaggtcaacgat	Protospacer
.*. ***.  *********** *******.****

78. spacer 15.19|2513609|34|NZ_CP045802|CRISPRCasFinder,CRT matches to NZ_CP039919 (Agrobacterium tumefaciens strain CFBP6626 plasmid pAtCFBP6626b, complete sequence) position: , mismatch: 8, identity: 0.765

tggaggacgcctgcgattttcccga---ggtcttgga	CRISPR spacer
cggaggacgccagccattttcccgatccggtcac---	Protospacer
.********** ** **********   **** .   

79. spacer 15.24|2513941|33|NZ_CP045802|CRISPRCasFinder,CRT matches to NZ_HG938354 (Neorhizobium galegae bv. orientalis str. HAMBI 540 plasmid pHAMBI540a, complete sequence) position: , mismatch: 8, identity: 0.758

gactgacgcacggcctgcggacgttcgcggaac	CRISPR spacer
ctttgacgaagggcctgcggacgttcgcgcgag	Protospacer
  .***** * ****************** .* 

80. spacer 15.30|2514344|33|NZ_CP045802|CRISPRCasFinder,CRT matches to NC_014213 (Meiothermus silvanus DSM 9946 plasmid pMESIL01, complete sequence) position: , mismatch: 8, identity: 0.758

tccacggcctcgagatccaacgggataccggcc	CRISPR spacer
ccatcagcgtcgagatccgacgggataccgact	Protospacer
.*  *.** *********.***********.*.

81. spacer 17.1|3884698|30|NZ_CP045802|CRISPRCasFinder matches to NC_008042 (Ruegeria sp. TM1040 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.733

ggcgccatttccgccgcagagcctgcacgt	CRISPR spacer
gcagccattgcagccgcagagcctgcggca	Protospacer
*  ****** * **************.   

82. spacer 18.1|4125593|34|NZ_CP045802|CRISPRCasFinder matches to NZ_CP015988 (Sphingobium sp. EP60837 plasmid pEP1, complete sequence) position: , mismatch: 8, identity: 0.765

tgggaaaggctcgcttgcgcagcggcctgttcgt	CRISPR spacer
ctgggaccactcgcttccgcagcggcctgttcgg	Protospacer
. **.*  .******* **************** 

83. spacer 24.1|5331237|34|NZ_CP045802|CRT matches to NZ_CP022569 (Rhizobium leguminosarum bv. viciae strain BIHB 1148 plasmid pSK05, complete sequence) position: , mismatch: 8, identity: 0.765

acggcggagcagatggcagagacgcgcgaatcgc	CRISPR spacer
acggcggagcagatggaagagatgcggagcttcc	Protospacer
**************** *****.*** .. *. *

84. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP015744 (Shinella sp. HZN7 plasmid pShin-08, complete sequence) position: , mismatch: 8, identity: 0.765

tcagcgtatcgccgatctcgccgccttcgcggag	CRISPR spacer
ccaccgtatcgccgatctcggcgccgagccagag	Protospacer
.** **************** ****    *.***

85. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_AP014705 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence) position: , mismatch: 8, identity: 0.765

tcagcg-tatcgccgatctcgccgccttcgcggag	CRISPR spacer
-cgccgacctctccgatctcgcggccttcgcggcg	Protospacer
 *. ** . ** ********** ********** *

86. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP032325 (Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence) position: , mismatch: 8, identity: 0.765

tcagcgtatcgccgatctcgccgccttcgcggag	CRISPR spacer
gctgcgcccggccgatcccgccgccttggcggag	Protospacer
 * ***. . *******.********* ******

87. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_LR536451 (Methylocella tundrae isolate MTUNDRAET4 annotated genome plasmid 2) position: , mismatch: 8, identity: 0.765

tcagcgtatcgccgatctcgccgccttcgcggag	CRISPR spacer
acggccgcttgccgatcccgcggccttcgcggag	Protospacer
 *.**   *.*******.*** ************

88. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP010410 (Xanthomonas sacchari strain R1 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.765

tcagcgta-tcgccgatctcgccgccttcgcggag	CRISPR spacer
-cggcgcgcccgccgatttcgccgccttcgccgac	Protospacer
 *.***.. .*******.************* ** 

89. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP046574 (Rhodococcus sp. WAY2 plasmid pRWAY02, complete sequence) position: , mismatch: 8, identity: 0.765

tcagcgtatcgccgatctcgccgccttcgcggag	CRISPR spacer
tgaaggtgtcgccgatctcgcggccttcggcgat	Protospacer
* *. **.************* *******  ** 

90. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP031918 (Escherichia coli O45:H2 strain FWSEC0003 plasmid unnamed12, complete sequence) position: , mismatch: 9, identity: 0.735

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
cctgccggttcagcgtcagcagcaggtctgcggg	Protospacer
* .* . *************.******* ***. 

91. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP012835 (Salmonella enterica subsp. enterica serovar Cerro str. CFSAN001588 plasmid pCFSAN001588_002, complete sequence) position: , mismatch: 9, identity: 0.735

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
cctgcatgttcagcgtcagcagcaggtctgcact	Protospacer
* .*  .*************.******* **. *

92. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_LT900339 (Gluconobacter oxydans 621H isolate WT-DSMZ plasmid 2) position: , mismatch: 9, identity: 0.735

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
acatgtcggtcagcgtctgcggcaggtccttgat	Protospacer
    **** ******** **********  .***

93. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NC_006672 (Gluconobacter oxydans 621H plasmid pGOX1, complete sequence) position: , mismatch: 9, identity: 0.735

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
acatgtcggtcagcgtctgcggcaggtccttgat	Protospacer
    **** ******** **********  .***

94. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP016613 (Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

95. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP021449 (Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

96. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to CP023013 (Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

97. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP049790 (Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

98. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP049794 (Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

99. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP049788 (Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

100. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022766 (Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

101. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP021763 (Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgttgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

102. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP015116 (Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

103. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP016555 (Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

104. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP049792 (Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

105. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052069 (Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

106. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP016915 (Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

107. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP016905 (Ralstonia solanacearum strain KACC 10709 plasmid unnamed1) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

108. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP025986 (Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

109. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022769 (Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

110. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP015851 (Ralstonia solanacearum strain YC40-M plasmid, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgttgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

111. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022773 (Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

112. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022783 (Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

113. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022791 (Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

114. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022795 (Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

115. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052071 (Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

116. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022482 (Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

117. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP009763 (Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

118. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to CP023015 (Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

119. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022779 (Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

120. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052075 (Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

121. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052085 (Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

122. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052095 (Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

123. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052105 (Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

124. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052077 (Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgttgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

125. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052087 (Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

126. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052097 (Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

127. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052115 (Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

128. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052127 (Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

129. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052079 (Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgttgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

130. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052089 (Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

131. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052093 (Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

132. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052101 (Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

133. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052099 (Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

134. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052107 (Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

135. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022781 (Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

136. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052117 (Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

137. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052125 (Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgttgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

138. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022793 (Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

139. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022785 (Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

140. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022787 (Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

141. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022756 (Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

142. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052129 (Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

143. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052121 (Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

144. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052123 (Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgttgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

145. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052131 (Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

146. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to CP011998 (Ralstonia solanacearum strain YC45 plasmid, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
ccgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
  * * .* ***.***** ***************.

147. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052073 (Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

148. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052081 (Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgttgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

149. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052083 (Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgttgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

150. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052109 (Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

151. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052091 (Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

152. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052103 (Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

153. spacer 6.7|921471|35|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP052119 (Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.743

ggggtctggggctgcggctcgctggtgctgctcgg	CRISPR spacer
acgctgcgcggccgcggcacgctggtgctgctcga	Protospacer
. * * .* ***.***** ***************.

154. spacer 15.10|2513017|34|NZ_CP045802|CRISPRCasFinder,CRT matches to MF417970 (Uncultured Caudovirales phage clone 7S_1, partial genome) position: , mismatch: 9, identity: 0.735

caattctttaataatggcttgaattgctttttct	CRISPR spacer
tctatctttattaatggcctgaattgcttcatca	Protospacer
.   ****** *******.**********. ** 

155. spacer 15.10|2513017|34|NZ_CP045802|CRISPRCasFinder,CRT matches to AJ972879 (Yersinia phage phiR1-37 complete genome) position: , mismatch: 9, identity: 0.735

caattctttaataatggcttgaattgctttttct	CRISPR spacer
tataaattaaataatggcttaaattgcttttctt	Protospacer
.*    ** ***********.**********..*

156. spacer 15.10|2513017|34|NZ_CP045802|CRISPRCasFinder,CRT matches to NC_016163 (Yersinia phage phiR1-37, complete genome) position: , mismatch: 9, identity: 0.735

caattctttaataatggcttgaattgctttttct	CRISPR spacer
tataaattaaataatggcttaaattgcttttctt	Protospacer
.*    ** ***********.**********..*

157. spacer 15.18|2513543|34|NZ_CP045802|CRISPRCasFinder,CRT matches to NZ_CP042998 (Aquisphaera giovannonii strain OJF2 plasmid pOJF2_1, complete sequence) position: , mismatch: 9, identity: 0.735

tgctacttgccggccatcgtcgactggccgttat	CRISPR spacer
ttgttgatgacggccatcgtcgcctggccgttcc	Protospacer
*  *   ** ************ ********* .

158. spacer 15.18|2513543|34|NZ_CP045802|CRISPRCasFinder,CRT matches to NZ_CP015739 (Shinella sp. HZN7 plasmid pShin-03, complete sequence) position: , mismatch: 9, identity: 0.735

tgctacttgccggccatcgtcgactggccgttat	CRISPR spacer
gtggactggccggccttcgtcgactggctggaat	Protospacer
    *** ******* ************.*  **

159. spacer 18.1|4125593|34|NZ_CP045802|CRISPRCasFinder matches to NZ_CP011600 (Phytobacter ursingii strain CAV1151 plasmid pCAV1151-215, complete sequence) position: , mismatch: 9, identity: 0.735

tgggaaaggctcgcttgcgcagcggcctgttcgt-	CRISPR spacer
cgtaaacggctcgcttgcgctgcggcct-ccggtg	Protospacer
.* .** ************* ******* .. ** 

160. spacer 18.1|4125593|34|NZ_CP045802|CRISPRCasFinder matches to NZ_CP011600 (Phytobacter ursingii strain CAV1151 plasmid pCAV1151-215, complete sequence) position: , mismatch: 9, identity: 0.735

tgggaaaggctcgcttgcgcagcggcctgttcgt-	CRISPR spacer
cgtaaacggctcgcttgcgctgcggcct-ccggtg	Protospacer
.* .** ************* ******* .. ** 

161. spacer 18.1|4125593|34|NZ_CP045802|CRISPRCasFinder matches to NZ_AP018757 (Metakosakonia sp. MRY16-398 plasmid pMRY16-398_1, complete sequence) position: , mismatch: 9, identity: 0.735

tgggaaaggctcgcttgcgcagcggcctgttcgt-	CRISPR spacer
cgtaaacggctcgcttgcgctgcggcct-ccggtg	Protospacer
.* .** ************* ******* .. ** 

162. spacer 18.1|4125593|34|NZ_CP045802|CRISPRCasFinder matches to NZ_CP051549 (Phytobacter diazotrophicus strain UAEU22 plasmid unnamed1) position: , mismatch: 9, identity: 0.735

tgggaaaggctcgcttgcgcagcggcctgttcgt-	CRISPR spacer
cgtaaacggctcgcttgcgctgcggcct-ccggtg	Protospacer
.* .** ************* ******* .. ** 

163. spacer 18.1|4125593|34|NZ_CP045802|CRISPRCasFinder matches to NZ_CP026198 (Enterobacteriaceae bacterium ENNIH3 plasmid pKPC-c606, complete sequence) position: , mismatch: 9, identity: 0.735

tgggaaaggctcgcttgcgcagcggcctgttcgt-	CRISPR spacer
cgtaaacggctcgcttgcgctgcggcct-ccggtg	Protospacer
.* .** ************* ******* .. ** 

164. spacer 18.1|4125593|34|NZ_CP045802|CRISPRCasFinder matches to NZ_CP026189 (Enterobacteriaceae bacterium ENNIH2 plasmid pENT-812c, complete sequence) position: , mismatch: 9, identity: 0.735

tgggaaaggctcgcttgcgcagcggcctgttcgt-	CRISPR spacer
cgtaaacggctcgcttgcgctgcggcct-ccggtg	Protospacer
.* .** ************* ******* .. ** 

165. spacer 24.3|5331368|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP039913 (Agrobacterium tumefaciens strain CFBP6625 plasmid pAtCFBP6625b, complete sequence) position: , mismatch: 9, identity: 0.735

gcgcaagcagttcgaggcgacgaaaaacactatg	CRISPR spacer
gcgcgagcagttcgaggcgatgaagcacgtcaac	Protospacer
****.***************.***. **...*  

166. spacer 24.3|5331368|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP039905 (Agrobacterium tumefaciens strain CFBP6623 plasmid pAtCFBP6623a, complete sequence) position: , mismatch: 9, identity: 0.735

gcgcaagcagttcgaggcgacgaaaaacactatg	CRISPR spacer
gcgcgagcagttcgaggcgatgaagcacgtcaac	Protospacer
****.***************.***. **...*  

167. spacer 24.3|5331368|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP039909 (Agrobacterium tumefaciens strain CFBP6624 plasmid pAtCFBP6624, complete sequence) position: , mismatch: 9, identity: 0.735

gcgcaagcagttcgaggcgacgaaaaacactatg	CRISPR spacer
gcgcgagcagttcgaggcgatgaagcacgtcaac	Protospacer
****.***************.***. **...*  

168. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP039965 (Pseudorhodobacter sp. S12M18 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.735

tcagcgtatcgccgatctcgccgccttcgcggag	CRISPR spacer
acacctcgccgccgatctcgccgccctcggggat	Protospacer
 ** * ...****************.*** *** 

169. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP025017 (Rhizobium leguminosarum strain Norway plasmid pRLN5, complete sequence) position: , mismatch: 9, identity: 0.735

tcagcgtatcgccgatctcgccgccttcgcggag	CRISPR spacer
gcaggccgaggccgaactcgccgcattcgcggag	Protospacer
 ***  ..  ***** ******** *********

170. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP054026 (Rhizobium sp. JKLM12A2 plasmid pPR12A205, complete sequence) position: , mismatch: 9, identity: 0.735

tcagcgtatcgccgatctcgccgccttcgcggag	CRISPR spacer
gcaggccgaggccgaactcgccgcattcgcggag	Protospacer
 ***  ..  ***** ******** *********

171. spacer 24.11|5331900|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_LT969521 (Pseudomonas aeruginosa isolate RW109 genome assembly, plasmid: RW109 plasmid 2) position: , mismatch: 9, identity: 0.735

taatcaaaatggcgacgtccgaccggctccgctt	CRISPR spacer
ggatcaaaatggctacgttcgaccggcgcgtcgc	Protospacer
 .*********** ****.******** *  * .

172. spacer 24.11|5331900|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP032256 (Pseudomonas aeruginosa strain AR_0111 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.735

taatcaaaatggcgacgtccgaccggctccgctt	CRISPR spacer
ggatcaaaatggctacgttcgaccggcgcgtcgc	Protospacer
 .*********** ****.******** *  * .

173. spacer 24.11|5331900|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP034355 (Pseudomonas aeruginosa strain IMP-13 plasmid pPYO_TB, complete sequence) position: , mismatch: 9, identity: 0.735

taatcaaaatggcgacgtccgaccggctccgctt	CRISPR spacer
ggatcaaaatggctacgttcgaccggcgcgtcgc	Protospacer
 .*********** ****.******** *  * .

174. spacer 27.3|5556430|34|NZ_CP045802|CRT matches to NZ_CP053709 (Acetobacteraceae bacterium strain PAMC 26569 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.735

cgatatagcaggcggagccggctggagggcgtta	CRISPR spacer
tgctggcgggggcggagccggcgggacggcgtta	Protospacer
.* *.  * .************ *** *******

175. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP025885 (Escherichia coli strain 503440 plasmid p503440_68, complete sequence) position: , mismatch: 10, identity: 0.706

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tttcagaattcagcttcagcggcaggtcatcgat	Protospacer
. . .  .****** ************** ****

176. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP027106 (Escherichia coli strain RM14721 plasmid pRM14721, complete sequence) position: , mismatch: 10, identity: 0.706

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tttcagaattcagcttcagcggcaggtcatcgat	Protospacer
. . .  .****** ************** ****

177. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP024583 (Roseomonas sp. FDAARGOS_362 plasmid unnamed2, complete sequence) position: , mismatch: 10, identity: 0.706

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
gccggccgttcagcgtcaccggcagggggtagaa	Protospacer
  ***.************ *******  .  ** 

178. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP017185 (Enterobacter roggenkampii strain DSM 16690 plasmid pDSMZ16690, complete sequence) position: , mismatch: 10, identity: 0.706

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagcatccagcttcagcggcaggtcatcgat	Protospacer
. . . *.*.**** ************** ****

179. spacer 15.18|2513543|34|NZ_CP045802|CRISPRCasFinder,CRT matches to NZ_CP033971 (Cupriavidus pauculus strain FDAARGOS_614 plasmid unnamed2, complete sequence) position: , mismatch: 10, identity: 0.706

tgctacttgccggccatcgtcgactggccgttat	CRISPR spacer
tggcgcttgccggccatccacgactggccccggc	Protospacer
** ..*************  ********* . ..

180. spacer 15.18|2513543|34|NZ_CP045802|CRISPRCasFinder,CRT matches to NZ_CP038636 (Cupriavidus oxalaticus strain X32 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.706

tgctacttgccggccatcgtcgactggccgttat	CRISPR spacer
tggcgcttgccggccatccacgactggccccggc	Protospacer
** ..*************  ********* . ..

181. spacer 15.18|2513543|34|NZ_CP045802|CRISPRCasFinder,CRT matches to NZ_CP043441 (Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.706

tgctacttgccggccatcgtcgactggccgttat	CRISPR spacer
tggcgcttgccggccatccacgactggccccggc	Protospacer
** ..*************  ********* . ..

182. spacer 18.1|4125593|34|NZ_CP045802|CRISPRCasFinder matches to NZ_CP042572 (Enterobacter hormaechei strain E5 plasmid pE5_001, complete sequence) position: , mismatch: 10, identity: 0.706

tgggaaaggctcgcttgcgcagcggcctgttcgt	CRISPR spacer
cagaaacggctcgcttgcgctgcggcctgcggtg	Protospacer
..*.** ************* ********.    

183. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP024310 (Sinorhizobium fredii strain NXT3 plasmid pSfreNXT3c, complete sequence) position: , mismatch: 10, identity: 0.706

tcagcgt----atcgccgatctcgccgccttcgcggag	CRISPR spacer
----cgccgaaatcgccgaactcgtcgccttcgcgctc	Protospacer
    **.    ******** ****.**********   

184. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP023064 (Sinorhizobium sp. CCBAU 05631 plasmid pSS05631b, complete sequence) position: , mismatch: 10, identity: 0.706

tcagcgt----atcgccgatctcgccgccttcgcggag	CRISPR spacer
----cgccgaaatcgccgaactcgtcgccttcgcgctc	Protospacer
    **.    ******** ****.**********   

185. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NC_016623 (Azospirillum lipoferum 4B plasmid AZO_p3, complete sequence) position: , mismatch: 10, identity: 0.706

tcagcgtatcgccgatctcgccgccttcgcggag	CRISPR spacer
ccagcgtcttgccgatctcgccgccgtaatagcc	Protospacer
.****** *.*************** * ...*  

186. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP013054 (Sinorhizobium americanum CCGM7 plasmid C, complete sequence) position: , mismatch: 10, identity: 0.706

tcagcgt----atcgccgatctcgccgccttcgcggag	CRISPR spacer
----cgccgaaatcgccgaactcgtcgccttcgcgctc	Protospacer
    **.    ******** ****.**********   

187. spacer 24.5|5331502|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP013110 (Sinorhizobium americanum strain CFNEI 73 plasmid C, complete sequence) position: , mismatch: 10, identity: 0.706

tcagcgt----atcgccgatctcgccgccttcgcggag	CRISPR spacer
----cgccgaaatcgccgaactcgtcgccttcgcgctc	Protospacer
    **.    ******** ****.**********   

188. spacer 24.11|5331900|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 10, identity: 0.706

taatcaaaatggcgacgtccgaccggctccgctt	CRISPR spacer
ccctgatgatggcgacgtcggaccgggtccgcga	Protospacer
.  * * .*********** ****** *****  

189. spacer 28.1|5717297|37|NZ_CP045802|PILER-CR matches to NC_041875 (Arthrobacter phage Jasmine, complete genome) position: , mismatch: 10, identity: 0.73

tcgccatccagaccactaccgatacctgctgaatatt	CRISPR spacer
tcgctatccagaccactaccgctaccgtcaccatcaa	Protospacer
****.**************** ****  *   **   

190. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP025922 (Escherichia coli strain 103605 plasmid p103605_83, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

191. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP025912 (Escherichia coli strain 204446 plasmid p204446_92, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

192. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP047309 (Citrobacter freundii strain L75 plasmid pCf76, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

193. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP017473 (Enterobacter cloacae strain M12X01451 plasmid pM12X01451, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

194. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP023348 (Escherichia coli strain ETEC-2265 plasmid unnamed2, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

195. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP019187 (Salmonella enterica subsp. enterica serovar Pomona str. ATCC 10729 plasmid pATCC10729_01, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

196. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_KT754161 (Shigella dysenteriae 1 strain CAR10 plasmid pCAR10, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

197. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to CP042948 (Escherichia coli strain 90-9133 plasmid p90-9133_1, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

198. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP017848 (Escherichia coli strain FMU073332 plasmid pEcoFMU07332d sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

199. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP019175 (Salmonella enterica subsp. enterica serovar Give strain CFSAN024229 plasmid pCFSAN024229, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

200. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NC_009787 (Escherichia coli O139:H28 str. E24377A plasmid pETEC_35, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

201. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NC_009790 (Escherichia coli O139:H28 str. E24377A plasmid pETEC_74, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

202. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP024244 (Escherichia coli O128:H27 strain 90-9281 plasmid unnamed, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

203. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to MH450052 (Escherichia coli plasmid pHN32wt, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

204. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to MH450053 (Escherichia coli plasmid pHN32_1, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

205. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP027332 (Escherichia coli strain 2013C-3277 plasmid unnamed1) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

206. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP041420 (Escherichia coli strain STEC711 plasmid pSTEC711_4, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

207. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP038299 (Escherichia coli O157:H7 strain TB182A plasmid pTB182A-5, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

208. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP053580 (Salmonella enterica strain 94-0093 plasmid unnamed, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tttcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

209. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NC_022333 (Escherichia coli plasmid pCss165Kan DNA, complete genome, strain: 4266 delta cssB::Km) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

210. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP029998 (Salmonella enterica subsp. salamae strain SA20053897 plasmid pSA20053897.3, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tttcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

211. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP030210 (Salmonella enterica strain SA20044414 plasmid pSA20044414.1, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

212. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP042531 (Klebsiella aerogenes strain C9 plasmid pC9_001, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tttcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

213. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022913 (Escherichia coli O6:H16 strain 2011EL-1370-2 plasmid unnamed1, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

214. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP022156 (Escherichia coli strain ABWA45 plasmid pABWA45_2, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

215. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP050381 (Klebsiella pneumoniae strain 51015 plasmid p51015_OXA_244, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

216. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to CP025909 (Escherichia coli strain 204576 plasmid p204576_83, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

217. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to CP025898 (Escherichia coli strain 500465 plasmid p500465_79, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

218. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP046347 (Citrobacter portucalensis strain FDAARGOS_738 plasmid unnamed1, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

219. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP024674 (Citrobacter freundii strain UMH19 plasmid pUMH19, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

220. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP029982 (Escherichia coli strain 99-3165 plasmid unnamed3, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

221. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP030780 (Escherichia albertii strain 05-3106 plasmid unnamed2, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

222. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP011595 (Klebsiella oxytoca strain CAV1099 plasmid pKPC_CAV1099, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

223. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP024250 (Escherichia coli O182:H21 strain D181 plasmid unnamed2, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

224. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP054617 (Azospirillum oryzae strain KACC 14407 plasmid unnamed3, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
gcgggtcgtccagcgtcagcggccggtggttgcc	Protospacer
   ******.************* *** . .* .

225. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to CP049614 (Escherichia coli O157:H7 strain K1516 plasmid pK1516-2) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

226. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP054717 (Salmonella enterica strain 85-0120 plasmid unnamed1, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tttcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

227. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP020338 (Shigella flexneri 4c strain 1602 plasmid unnamed2, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

228. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP044100 (Citrobacter werkmanii strain FDAARGOS_616 plasmid unnamed1, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

229. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_LT985275 (Escherichia coli strain R71 plasmid RCS70_p, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

230. spacer 6.6|921404|34|NZ_CP045802|CRT,PILER-CR,CRISPRCasFinder matches to NZ_CP025918 (Escherichia coli strain 120899 plasmid p120899_76, complete sequence) position: , mismatch: 11, identity: 0.676

cgcggtcgttcagcgtcagcggcaggtcagcgat	CRISPR spacer
tctcagaatccagcttcagcggcaggtcatcgat	Protospacer
. . .  .*.**** ************** ****

231. spacer 15.13|2513214|33|NZ_CP045802|CRISPRCasFinder,CRT matches to NZ_CP039644 (Azospirillum sp. TSA2s plasmid p2, complete sequence) position: , mismatch: 11, identity: 0.667

tcatatatgcaaatgatggaagctgtgcatgca	CRISPR spacer
gatcgtatgcaaatgatcgatgctgtgcaaatg	Protospacer
   ..************ ** ******** ...

232. spacer 15.17|2513479|32|NZ_CP045802|CRISPRCasFinder,CRT matches to NZ_CP053347 (Sphingomonas sp. AP4-R1 plasmid unnamed1, complete sequence) position: , mismatch: 11, identity: 0.656

accgagccagagccgcgaaaaggagaagaggg	CRISPR spacer
ctcgacgcagagccgcgaaaaggagcgttctc	Protospacer
 .***  ****************** .     

233. spacer 15.17|2513479|32|NZ_CP045802|CRISPRCasFinder,CRT matches to AB624551 (Enterobacteria phage FI genomic RNA, RNA-directed RNA polymerase beta chain region, isolate: 110112RS393) position: , mismatch: 11, identity: 0.656

accgagccagagccgcgaaaaggagaagaggg	CRISPR spacer
ttcgagcgagagccgcgaaaatgagcgactct	Protospacer
 .***** ************* *** ..    

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	1759147 : 1844134	51	Tupanvirus(50.0%)	tRNA,coat,protease,holin,transposase	NA
DBSCAN-SWA_2	2346932 : 2356127	11	Staphylococcus_phage(50.0%)	NA	NA
DBSCAN-SWA_3	2458245 : 2466755	11	uncultured_Caudovirales_phage(44.44%)	tail,plate	NA
DBSCAN-SWA_4	2561313 : 2569960	10	Staphylococcus_phage(50.0%)	NA	NA
DBSCAN-SWA_5	2820933 : 2831696	10	Bacillus_virus(12.5%)	NA	NA
DBSCAN-SWA_6	4288697 : 4359054	52	Brevibacillus_phage(46.67%)	protease,portal,tail,coat	NA
DBSCAN-SWA_7	4966897 : 4976580	8	Synechococcus_phage(28.57%)	NA	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP045802|1759147:1844134|DBSCAN-SWA
TTTAAAGGCTGTCCGTCGCTTCCGTCATGGTGGTGCTGGTTTCCTGCTCCTCCGAGCCGGCGCCCTGAGTGGCTTTCTGCTTCTTCCACGCCTTGAAGTCCGTCATGTCCATGTACGGCTTCTTCGTCATCCAGTACTCGTTCTCTTCCATGAGCATGGCTCCGATGAGACGGATGACGGAAGCGCGATTGGGAAAGATGCGGATGACCGTCTCGCGCCTGCGGATCTCCCCGTTCAGGCGTTCCATGCCGTTGGAGGTGCGCAGCCGCACGCGGTAGGCCTCCGGGAAGGCCAGCACCGCGACGGCGTCCTCGAACCCGTCCTCCAGTATTTTCATCGCTTTGGGTGCTGTCTCGGCATACGCCTCAAGCGTCTGTTCGAGATAGGAACGAGCCGTCTTCATGTCGGGCGCATCGAAGATCGATCGGACGCGACTCTTGATTTCGCTTTGGAGCGCTTTGGGCGCTGCGTTCAGCACGTTCTTGATGAAGTGCGTCTGGCACCGCTGCCACGAGACCCCTTGAAACTCCTTCTCGATGGCCTTGACCAGCCCGCCATGATAGTCGCTCGTGACGAGCTCTACGCCGTGCAGGCCGCGCTCTTTCAGCCAGCGGAAGTAGGCGCCCCAGCTCTCCTCCGACTCGGTGTCGTCGACGCGCAGGCCCAGAATCTCACGCCGGCCTTGCTCGTTCACGCCGTAGCCCACCAGAACGCCTCGAGAACAGATACGGCCTTCTTCACGCACCTTCACGTAGATCGCATCGATGGTGATGAAGGGGAAGGCGTGGTCGGCCAGAGAGCGGTTGTTCCAGTCGTGGACAGCCGGGTCCAGCTGCTTGCACAGGTGGCTGACCGTTGACTTGGAGAACTCGGTTCCGCACAGCTCCTCGGTGATTTTAGTCACCTTGCGCGTCGACACGCCGTTGATGACCATTTCCATGAGCGAGAGAACCAGCGCTTGCTCGCTGCGCTGATACCGGGCGAAAAGCTCGGTAGAAAAGGAGCCGTCCCGAAACCGGGGGACGCGCAAGGTGACGCTGCCAGCGCGGGTAATGACGTCGCGCTCGTAGCTGCCGTTGCGATAGCCCTTGCGCTCGCTGGTGCGCTCGTACGTCTGCGCCGCCAGCTGATCTGTCGCCTGGGCTGTCAGCACCTGATTCAGCACCGTCTCCAACAAGCGGGCCACTCCCGCGTCCCGATCGGTTCCGATAAACAGCTGGTGCAAAATGTCCTGATCTACGGTAATCTGGTATTGAGTCATGTGTAGGCACTCTCCTTGGAATGTTGGTCTCGACAACTTCCATTCTAACCGAGAGTCCTACCATGGCTTTTCTTTTTATGGTCAGGAGCATTTTACACAATTATATGGACTTAACTGGTTTCGGCTTCCGCTAGCCCGAGTTACGCAGTTTTTCCGAGCAACTCCGACCGTATCGGCCCCCACTTGCCCGAGTTACTCGGTTTTTCCGCGTAACTCCGACGGGTGCGGCACCCACTTGCCCGAGTTACGCGGTTTTTCCGAGCAACTCCGCCGGGTTCGGCCTCCGCTCGCTCGAGTTACTCGGTTTTTCCGCGTAACTCCGACGGGTTAGGCCCCCGCTAGCCCGAGTTACGCGGTTTTTCCGAGTAACTCCAACTGTTTCGGCCCCCGCTAGCCCGAGTTACTCGTTTTTTCCGCGTAACTCCGCCCGATTCGGCCCCCGCTAGCCCGAGTTACTCGTTTTTTCCGAGCAACTCCAACCGTTTCGGCCTCCGCTCGCTCGAGTTACTCGGTTTTTCCGCTTAACTCCGACGGGTTCGGCCTCCGCTTGCCCGAGACGAGGGAGTCCACGTTCTATGGATCGCGCGAGCGATTTCGATACGGGCCCAAGTCGTTGCAGCCTGGGTAAGCTCCAGCAAGTGGGAGCTGCTTTCAGGCTCTTTTCGCAGCGGCCGTTCAATGACAAATAATCCTGCTGGATAAGGTGCTAGGTGCGGTCTGGAGGTTATGGTAAACTATTCCCAAACGAACGGCGAGGGAGGAAGGACGATGACGAGAGGCAAAGTACCCCGCTAATCCCGTAAGAAGACCGGAGCAAAAACTTGGGCCGACGTCCGCGTACGCGCCAGATCCGGCTGCAATGTCGGCGTCCGTACAGTCGTCAGAGCTAGCTGCAATGCCGGCGTCCGCGCACGCGTCAGAGCCGGCTGCAATGCCGAAATTCGCGCAAACGTCGATGCTATCGCTCGCGGAGCCGAGCGTGCCCGCGCTCCTCCCTGCGCTTTCCTGTCCGGTCGGAACGGAGGAAACGCAAAGGGGAGGATGACGAAAATGAGAGAACGGAACGATTGGAACGTTGCTCACGGAATGGAGGAGCGCTGGCGGGAGCTGCGCTTCGGGCTGGAGATCGAGTTCGTCGGCGGCGAGCCGGAGCGGCTGGAGCTGCTGCCGGGCTGGACGATGGCGCTGGACGAGAAGCAGATCGACGGAGACGGAGAGGCGTCGGGCAGCGAGCTGCAGTCGCCGCCCCTTCGCTGGGAGGAGCTCGATCAAGCGGAGGCGATGCTGGAGCGGCTGAGGCGGCAAGGGGCGCAAGCCAACTGGAGCTGCGGCCTGCATGTGCATGTCGGGCTGGAGCCGTTCGGCGAAGCCGCGCTCCCGGCGCTGCTGGAGGCGGCGCTGAGCTCGCAGGAAGCGCTTAGCTCTCTGCTCGGCACGAGCCCGCACCGCCGCTTTTATGCGCCGCCGATCACGGCGGAGATGGCGGAGGCTTTCCGCGCCAGCGGCGATCTGGCGGCGCTGAGGCGCAGCGGACGGCCGCAGTCCCATCGCTGCGGCATCAATCTGAGGCCGTGGAGCGAGATCGGCACCGTCGAGATCCGCTACGCGAATGGAACGCTCGAGGCGGCCGAGGTCAGGCGCGTTGTCGAGCTTTGCCTCCGGTTCGTGGACGGCGCCTGCAGAGGGCAACGCATGCCGGATGAGCCGGCGGCTTTGGCCGCCGCGCTCGGCGCGCCGTCCGGCGGTTACCCGCCGCGCGCCGATCCGCCTCGCTGGCATCGCGAGCGGATCGCGCTCGAGAACGCCCTGCTGCCGCAGCTTGCGGCACAGGCGGCGGAGCTCGTGCCCGGCGGCGAGATCCATCACATCGTCGCTGCGGACGGCGGCGTCATGGTAGCGGTCGAGGATGAAGAAGGCTCGCTGCATCGGTTCCGCTGCGCGCTTGCCGCCGGCGGACTGGAGCCGCTGGGCGACGGATAATCAGGAGGGAGTGGAGTCCGGATGGAAAGGGAACTTCAGGAAATTCAGGGCAGGCTGGCCGCAGAGCTGGCTGCCGCGCTGCAGGAGCGCAGGCTGCCGCTGGCTCCGGACGGGAATCCGATCGTCGAGGAACGCGAGCGGCGTCTCGACCGGGAGGCGGCGCGGCTGCTGGAGCTGCGTGAGCGCCGGATCGGGGAGGAGGAGACGAGGCTGCGGCTGCTGGCGCTCGTATCGGGCCTGCATTTGCGCAACGGCAGCTTGAACCGCTCGCATGAGCTGTCGCAGGAGCTGGACGGTCCCGACGGCAGCTATCTGCACGGGATGATGCACCGGATGGAAGGGGACTTTTCCAACGCGAAGTATTGGTTCCGGCTCGCCGGCCCGCATCCCCGCGCCGAGACCTGGCGCCGCCGGACCGAGCAGCTGCTCGACGGCACGCCGGATGCGGAGCCGGCTCTCGCCCGCCGGCTGCGCCGCGAGCCGGGCGTGGACCCGGCGCTGCTGACGGACCTGGCGGCCGCCTCCGCGCTGACCGGCCATGCCGGAGCGGATACGCCGCTGCTGGAGCGGGTTCAGGAGCTGGAGCTGGAGCTGCTGCTGGAGGCGCTGGCTGAAGCCGGCGAAGACCGGTCATGAGCGAAGGAATGCTGCCGGTCGTGTGGCTGCTGATCGCCGTCGCGCTCATGGCCCAGCCGGTCTACCGTCTGACCCGGCGCATCCGCGAGCTGGAGGACAAAGTGCGGGAGCTCGAGGCGGAGGTCCGCACTCCGAGCCGGAGACGGAACAACCTGCGCATGCTGGACGGGGGAGACAAGGAGAGCTGACGCATTTCGGGCCTTGCCTGCCCGGGAGCGGCCGCATTTTTGAAAAGGGGCGGTTCCAAGGTCGTTTTCATCGACCTTTGGAACCGCCCCTGCTTTTTCAACATGCAAGAGGCAGCCGGCGCGCCGCGAGCGACGTGCCGGCTGCCTCTTGCTTGGAATCGCGGTCGGCCCGGAGCCGCGCCGGCCTCCGGCCTAAACGCCGATCAGCTCGCCGTCGCCGCGCAGCGCGGCGGCCCGATGGAGCTTGTTCGCATGGAAGTAAGCCGTTCCTTCCAGCCTGCGGCCGTCCTTCGTCAGCGCTGACACCTCGACGCCGATGTCCGATGCCGTATAGAAATAGTCCAGCAGCTCGCTGTCGGCCACTCCGTTCACGTCGATATACCACAGCCTCGAGCCGGCGTCCGTGACGAGCGCCAGCTCGGCCGATTCCATCTCCAGCTCTTTCGTCCAGCCGCCATGAGTCAGCGTCAACAGCAGCAGCGGATACGTTTCCATGTCGATTTCTCTCCCGTCTGCTCCTGATTGTACCTGCGGCACTGCCGCGATGCAACCTTTCGGAGCGGGCGTCCGTCCATCACAGCAAGATCCAGAATTGGGCCTTGATCCCACAGGAAAGAAACCGGGGGGCGATGAGCATGAAAAAGAGAAACGACGAGCCATCGGGCATGGAAACGAACCGGCAGCCTGCGCCAGAGAGCGGCCGAGGACTCCGATGGACCAAGATCGGTCCGCGGCTGAAGCTGGCCACGGCCAGCCTGCTGATCGCGGCGCTGCTGACCGGCTGCGGCGCGGCGGATGAAGGGGCGGTCCCGGGGAGCGGGGAAGCTGCTGCAGGCGGAGCCGCCGCCGTAGACGCGGCCAGCCGGGAGTCCGTCGCCGGCGCGCCGCAGAAGAGCGCGGCGAAAGAGGCTCCGACTGGCGCTGCCGCGGCGCAAGGGAGCGAGGAGCCCTCTGCGGCTGACGCATCCGCCGCAGAAAGCGCTGAGCTCCAGCATTCGGACGCCATGCCTCCAAAGGCAGAGCCGCGGCAAATGCCCGAACCGCAAGCCGGCATGCTGACGGCAGGAGAATGGGACGATCTCGGCGCGTGGAGCCGCTGGACGGAGCTGATTCAGGACAGTCCTTATCCGGCTGCCTGGGGCTTCGCCCCCTATCGCCGCCTGACGGTGCAGGCGACGGCCAAAGGCAAGCCGGCACGGGACGTCGAGGTCATCCTGCAATGCGGCGGCAAGCGGGAATGGACGGCTCGCACCGACGGCAAGGGACAGGCGACGCTGTTCGCGGGACTGCTCGAGTCGCGAAGCCGGCAGGACGTGGAGCTGCAAAACGAGCCGGCTGCTTCGAGCGAGCAGCAGGGAGGCTCAAAAGATCAGGCCGCCGCGCCTCAGGACTGCTCGGTCCAAATCGACGGGGGGAACGGACTTCTCGTACGAGAAGCGGAAGCGAAGGATTGGGCGGGGCGGGTCATGAAGCTTGAGACCGACCGGGAAGCGGCGCAGCCGGACGCCGTGCTCGACCTGCTGCTCATGATCGATACGACCGGGTCGATGGCCGACGAGCTGAGCTATCTATCGACCGAGCTGACGAACGTCGTCTCCCGCGTCAAGAAAAACATCGGGCAGAACCTGACCGTCCGGATCAGCCCGAACTTCTACCGCGACCACAACGACGAGTATGTCGTGCGGTCGTTCCCGTTCCTCGAGGACGCCGTCAAGGCGCAGGCGCATATCGCCCGCCAGGAGGCCGACGGCGGACAGGATTACCCGGAGGCGGTCGCCGAGGCGCTGACCGATGCCGTGCTGGAGCATGATTGGAGCCGCAGCGCGAGGGCGAGGCTGATGCTGCTCGTGCTCGACGCTCCGCCCCACCAAGGACTTCGGGAGCGCGAAAGCATCCAGCATGCGGCCGCCGAAGCGGCGAAGCAGGGCATCCGCATCGTGCCGGTCGCCGCGAGCGGCACCGACCTGGAGACGGAGCTGCTTCTGCGCACGCTCGCCGTCTCGACCGGCGGCAGCTACGTGTTCCTGACCGACGACAGCGGCATCGGCAACGGCCATAAGCAGCCGGAGGGCGTCGAGCCGCAGATCATGCCGCTGAACGATCTGCTCGTCGATCTGATCAGCCGGCACGCGGAGGGCTGAGCCCGCCTGCATCCGCCCGATCCTCCCTTCCCGCAACAGCACCAGCCCGCTTCCGGCATCCGCCGGAGCCGGGCTGTTCAGCATTTCCATCGTGTATTCCGATAATGAACTAGCGGCTATCCTCCTCGTGAGGGAACGATTCACGCCGTCCGATCAGCCATCAGGAAGGAATCGACATGAAGAACCAACTGCTCCTGCTCGTCGGCTTGGTCCTGATTTTCGCGGCCGCCGCTTCCATCGTCGTCTACTACTGGCTCCATCCCGTCGAAAACTACCCGCAAGCGCGAGCGGGCGTCCTCGACGCCCGCGATTGGGATTTTACGAAGCAAGGCGTCATCCCGCTGCAGGGAGAATGGGAATTTTATGAAGACAGGCTTCTAACGCCGGCCGATTTCGCCCAGAGCGAAAAGGAGCTGGAAAGCGGACGAAGCCTGCTGAACGTGCCCGGCAACTGGAACTCGGCGGACGGCTTCGGCGCGGGAACGTACCGGCTCCGAATCGAGGTGAGCGAGCCGGGATATTACAGCGTGAGAGCAAAAAAGATCCGCCTGTCCAGCCGCATTTACGCGGCGGGGGACGAGCTTGGAGGCAGCGGAACGCCCGCTGCGGACCCGAGCCGCTTCGTGCCGAGCAATCTGCCCGTCCTGGGGACGGTCAAGGCGGAGAGCCGCACGATCGACATCGTCATCCAGGTGGCCAGCTACCGGTATTTGCCGGGCGGACTCGTGCAGCCGCCGGAGTTCGGGCTGGCGGAGGAGGTGGCGGCCAGGCGAGACGTCTCGCGCATGGGCGACATGATCCTCGTCACGGCCCTGCTCGTCTTCGGCCTTTATTTCGCCGGCATGTTCAGGCAATGGAGGCGCGAGCCTTACCTGCTCTACTTCAGCCTGTTCTGCCTCTCGCTCGGCCTGTTCTTCAGCATCGACAACGAGATCGTGCTCGCGTCGCTGCTTCCGTCGATCTCGTTCCCGGCGCTGCAGAAGCTGCTCTTCATCGTGCCGTCGCTGTCGATCCTGTTCTTCATCCATTACGTCCGGCTGTATTTGGACGACAAGCCCGGCAGGGGGCTCAAGGCGTTCCTGGGAGCGAGCTACGGCTTTCTGGCCGTGCTCATCTTCATTCCCAACGAGGGGCTCGTTCCGCTCCTGTGGCCCGGCATCCTCATGCAGACGCTCTCGTTCGTCTTCATCTTCACGTCGATCTTTCGCAAGCGCCATCTCGGCGCAAGGGTCTATTCCATCCTGCTCGGGACCTTTTTCCTCATCATCAGCTGGGTGTTCGCGCAGACGCGCTATCAGCTGGCGCTGGACAGTCCCTACTACATGGTCGTCACGCTGCTGCTCGTCGTGCTGTCCCAATCGTTCCTAATGTCGGACCGGCTGCGCTCCGCCTTTGTGCAGAGCGAGCGGCTCTCCCGAAGACTGCTGATCCAGGATCGGCAAAAGGATGAGTTCCTCGCCAAGACGTCGCATGAGCTGAGGACGCCTCTGCACGGCATCGTGAACCTGTCCCAGTCGCTGCTGGACCAGGCCGAGACTCCGCTCCAAGCGGAGCATCGCGACAACATCCTGCTGCTGAATCGGCTCGGGAGGCGGCTCGCCGGCCTGGTGGGCGACATCCTCGATCTGAATCGGATCCGCTATGGGGAGCTGCGGGTGCAGCTGAGGCCGGTCGACATGCGCGTCTCCGCCGAATTCGTCTGGGAGACGCTGGCGATCGCATCGGTCAATCCGGGCATTCGGCTGCTCAACGAGCTGCCGGCGGAGCTGCCTCTCGTCCTCGCGGACGAGAATCGGCTGCGCCAGATTTTGCACAATCTGCTCGAAAACGGGCTGAAATACACGGAGCGCGGCACGGTGTCGCTCTCGGCCGCACGGCAGGGGGACATGCTGGCGGTGACGGTCAGCGACACGGGCCGGGGAATTCCCCCGGAGCTGCGGGAGGAGCTGTTCCAGCCGTTCGTCCATGGCCGCGAATCGGGGGCGGGCTCGCGCGAGGGCATCGGACTGGGGCTGAGCATCGCCCGGCAGCTGGTGGAGCTGCAGGGCGGCGCCATGTCGCTGGAGTCGGAGGTCGGACGAGGGTCCAGGTTTACGTTCACGCTGCCGGTGGCCGATGCCGGGGAGCGGCCAGCCGGGGCTGCCGCAGCGCCCTCCTCCGCCATGCGGGCGGAAGGGAGCGAAGCTCGGCACGGCGCTTCGGCGCCGCATCCGATGCGCATGGGCGAGGGCGGCGGCTCCGCAGCGGCCCTGCACATTCTGATCGTCGACGACGAGCCGTCCAATCTGAAAGTGGCGCTGGACGCGGTCTCCTCGCTCGGACATCGCTTCACTGCGGTCAGCAGCGGAGCGGAAGCGCTCGAGGCGCTGCGGCGCCGGCAGCCGGATCTCGTGCTGCTCGACCTGATGATGCCCGGCGTGTCCGGACTGGACGTCTGCCGGGAGATCCGGTCGCTGCACGGACTGTCCGAGCTTCCCGTGCTCATGCTCACCGCTTCCGGCCAGACCGCAGACATTGTGGCCGCCTTTGCCGCCGGCGCCAACGACATTCTGCACAAGCCGTTCGAGCTGGCGGAGCTGAAGGCCCGCGTCCAGTCGCTGCTGGCGATGAAAAGCTCCTCGGAGCAGGCGGTGCGCCGGGAGATGGACTTCCTGCAGGCCCAGATCACCCCTCATTTCCTGTACAACACGTTGAATGCCCTGATCGGGCTGAGCTACAAGGACGTGGACAAGCTGCGCGAGACGATCGAGCATCTGACGACCTATTTGCGCGCCAAGTTTACGTTTGTCCTCGCCGAAGCGGTCCCGCTGGAGCGGGAGCTGGAGCTGGCGCGGGCTTATCTGGCGATCGAGCAGCTGCGCTTCGGCCCGCGGCTGCAGGTGGAATGCGTCGTCGACGAAGGAGCGCGCGCGCTCCTGCCGCCGCTGACCTTGCAGCCGATCGTGGAGAATGCCGTCCGCCACGGCATCGGGCCCAAGCCCGAGGGCGGCACGGTGACGGTCTCGATCCGCAGCATCCCGGTTGGGGTCGAGATCCGGGTCGAGGATGACGGAGTCGGCATGGACGAGGCGATGCTGGCCAGGCTGGAGGCCGGGCAGGCCGGCGGCATCGGCATCGGCAATGTCAACCGCCGGCTGCAGATGAGGTATGGGCGCAAGCTGGACATCGCCAGCCGTCCGGGGGCGGGGACCCGAATGACGATGATCGTGACGAAGGAGGAGCGCGCGTGAGGGCGATTTTGATCGACGATGAAGAAATAGCGCTCGATGTCCTGGAAATCAAGCTGAACGAGGCGGGCGGAGTGGATGTCGTCGGCAAGTTCCAGCGCGTGGCGGACGCGATCTCGCAGTGCGGCGCGCTGCAGCCCGAGCTTCTCTTCCTGGATATCGAGATGCCCGGCATGAATGGGCTTGAAGCCGCCGCGGCGCTGCGCGCCGTCTGCCCGGACGCCGAGGTGATCTATGTGACGGCCTACCACCATTATGCGGTGGATGCGTTCGGCACGGAGGCGATCGGCTATCTGCTCAAGCCCGTCGCCAAAGACAAGCTGCTTCAGGCGCTGTCGCGCTACGAGAGCCTGCGGGCCCGGCTGCGCGATCGCAGCGGCGCCGGTCAGGAGCCGAGCGGCGCGACGACAGGGAGGACCGGGACCGGGCAAGCCAGTCCGCTCGACCTCGTCCCGCCGCCGGATTCGCCGACGCTGTCGCTGAAGGTGCTGGGCAGCATGGAGCTGTACGGCGGGGACGGCCGCCTGCTCACCTGGCGCACCCGCAAGACCAAGGAGCTGTTCGCCTACCTCTGGCATCATCGCGGCCGACCGGTCTACAAATATGCCATCCTGGAGCATCTGTGGCCGGACGATTCCGCGGAGCGGGCGCAGAAGCTGCTGCATACGTCGCTCTATTATTTGCGGAGCCTGCTGAAGGCGGAGGGCTGCGGGGAGATCGTCCACTATGGAGACGAGCGGTATTGGCTGGACGCGGGCGGCATCCGCAGCGATCTGGAGGAGCTGCTGGAGCGGTCGAAGACCGGCTTGGAAGGGGAGGCCGGACAGGACGCGGCGGGGCTCTACCGGGGCGACTATCTGGAGACGGAGCATTACCCGTGGGCGGACGCGTACCGGATCGAGCTGCGCTCCTCGTTCACGGCGGCGCTGAGAGCCGGCCTGGTCCAAGCCGGCTCCGCGCAGCGGCTGGCGCTGCTCGGCAAGCTGATCGAGCTGGAGCCGGAGCATGGCCCGTATTACGACCTGCTGGCCGAGTCGCAGGAGCAGATGGGACATTGGAGCGGCGCGCGCCAGGCGCTGGCGCTCAAGGAACGGATGGGACGGGAGTAAGGCTGGCCGGCCGGGACGAGCAAAGGCCGGCTGCAGCAGGAAACGGCTGTCGAAGCATCATTCGACAGCCGTTTTTGTCGTTTTTTGGCGAGATTGTTGTGAAAGTGTTGAGAATCGCCCTGCTACACTGGACGAGGCGGAACGCAATCACTCAAGGACAAGGTGGGAATACGAATGAAAAAATGGGGATCGCTTCTCCTCGTCATCGCGATGCTCTTCACCGCCGTGCCGACGGCATTCGGTGCCGTCCGCACGGGCTGGGACCTGAAAAGTCCTCGCGGCATCGCGACGGACAGCAGCGGACGCATCTATGTCGCGGATATAGGCAATCATCGAATTCAGGTCTTCAACGAAAACGAGAGCTTGTCGATGACGCTGGGCGAAACGGGGATCAGAGGGGCGGACAACGCCCATCTGGATACGCCGACGACGGTAGCAGTCGATGCTGCGACGGGAGAAATCTATGTAACGGATACTTCCAACAAGCGCATCCAGGTGTACAGCAGCCAAGGAAGCTATCTCCGCAGCCTTGCTCTTCCAGCCAGCGCAGTGTCGGAGTCTGTCGCGCTGGACGGCCTTGGACATGTCTTCGTGACGGACCACAACAACATGATCTACCGCTTTAATACGGACGGAAGCGGCTATAAGCAGCTCTTCGGCTATCCCGATGTAGACTACAGGCCGCTAGGAATCGCGGCGGATTCCAAGGGAACGTTATACATCTCCCAAGTATTGAGAAACACGATAGTGGTATACACATACAATAAAAGCCAGGACAAGTACACGTATCAGAAGACGATCGGTGAGAAGGACAAACCGGGCACGGACAACATGCATTTCAATCAGCCTTGGGGCGCGCATGTCGACCGCGACGATCGCCTTTATATCGCCGACGGCGGCAACAAGCGGGTGCAGGTGTATAACAGCGACGGCAGTTATCACATGACGTTGACAGCCCCGAGTCTGACCTCCCCTTACCATGTGGCGACAGACCGAAACGGCACCATCTATGTCAGCGACAACCATAGGTCGATCCTGATGTTCGACGCGCAGGGGCAGTTCGTGAAGACGCTCGGCCAGAACACCGTTCCGGTATTCGAGGGCAGCCAGACGGCGCTTGCGGTCGCGCAGGACTCTTCGCCGACGGATGTCAGATCCTTGCTGAAGGTCACGGACAGCGACAGCGGGCAGACGCTGAGCTGGACGCTGACGACAGCGCCGACTCATGGAGCCGTCAGCCTCGGCCAAGGCGTCGCTGCCAGCGGAGGCTCCGGGCTGACGCCGGCCGATGCGATCGAATACGAGCCGGCTGCAGGCTATTTCGGCACGGACCAGTTCACGGTCACGGTCAGCGACGGAGCGGGAGGCTCGGCTGCCCGCACGATCAACGTCACGGTGAGCCGGAAGGCGGCCGCGCCGACAGCCGATCCGGCCAGCGGCTCCGTCGTGGCGGACGGCAGCGGCATCGCTCTTTCGACGACGACGCCGGGCGCGTCCATCTACTATACGACCGACGGCACGGAGCCGACGACGGCCAGCGCCGCCGGCACGGCAGTCGCCGTCAGCGGCGCTCCCGGCGAGACCGTGACGGTGAAGGCGTTCGCGGCAGGGCCGAATCTGCTCGACAGCGACGTCGTGACGTTCTCGTATGTCATCGAGACGCCGAAGTCGAGCAATGCCGATCTGCAAAGCCTGTCGCTGTCGGCAGGAGACTTGAGCCCGGCCTTCTCGAGCGGCACGACCCGGTACTCGGCCAGCGTGGCCAGCGAGATCTCCAGCTTGACGGTCACGCCGAGCGTGGCGGATGCGGTGTACGGCACCGTAGCCGTCAGCGTGTATGATGGAACGGGCAAGCTGACGGGCGGACCTCATGCCTTGAGCGGAGGGGGAGCCTCGCCCGCGCTGCCTCTGGCGGCAGGCGACAACGTCATCGAGATCCGGGTGAGCGCGCAGGACGGCAGCATGCTCATCTATACGGTGAGCGTGCAGAGAGCGCAAGCAACGGAAACGCCGCAGCCGGAACAGCCGACGGAGGAGCCGACGCCGACGCCAACGCCGGTGGAATCATCGACTCCGACCCCGACTCCGGTCGAAACGCCGACGCCGACACCGACAGCGACGCCGACACCGACAGCGACGCCGACGGCCTCTCCCGGCCTGAGCATGACGGTGAACGGCCAGCCGAAGGGGCAGCTCGTGCAGGCGGCGACGGAGCAGACGAACGGCCAGACGATTCTCGTCGCGTCCGTCAACCGCGCGCAGCTGCTGGAGCAGCTGGCGGCTGCGGCTGACGGGGCCGTAATGGCGATCCCCGCCGCGAACGAGCCGGTCGACGGCGTATCCGTCCGCCTGACCGGCGATGTCGTCCAGGCGATGGCCGCCCGCAAGGCGCAGCTGCAGGTGCAGGCGCCGAGCGGCACCTACGCGCTGCCGGCGGGACAGATCGACATCGCGAGCCTGGCGGCGCGGTTTGGCGCTGCGGACCGCCTGTCGGAGATCCTGCTGCGGATCGACGTCGTCCAAAGCGATGCGGCGACAGCCGAGCTGGCGCGGCAAGCCGGCCTTCGTCAAGGCTTCCACGTCGCCGCGGCGCCGGTGACGTTCGAGGCGGCGGCTGCCTTTGACGGCAAAAGCGTCGCGATCGACCGCTTCAGCTCTTATGTGAAGCGCGAGCTGCCGCTGCCGCAAGGCGCGGATCCGGCCAAGATCACGACCGCTGTCGTCATCGGCAAGGACGGTACGGTCCGGCATGTGCCGACCTTCATCGAGATGCGGGACGGGGCGCAATACGCGATTGTCAACAGCTTGACGAACAGCGCCTACGCGCTCGTCTACCATCCCGCCGCCTTCGCCGATGTCGCGGGGCATTGGGCGGAGCCGGCCGTGAACGACCTGGCCTCGCGGATGGTCGTCAGCGGCGTTGACGCCGAGCATTACCGTCCGGATGCGGCCGTCACCCGCGCCGAGATCGCCTCGATCCTCGTGCGTGCGCTTGGCCTCGCTCCGAGCTCCGCCGCTTCGCCGTTCGCCGATGTCGACGCAGCGGCCTGGCATGCGGGCTCGATCACGGCGGCGCAGGCGTACGGCCTCGTCCAGGGCGACGGGCACGGCTCGTTCAACCCGAGCCGCAGCGTGACCCGCGAGGAGGCTCTGACGATGCTGGCCCGAGCGATGGCGATCGCAGGCATGGACGCCAGCGGCGCAGGCGCCGATTCCCTGGCTGCGCACCGGGATGGCGGCCAGGTCAGCCTATGGGCGCAGGATGCGTTCGCGGCCGCTTTGCGCCACGGACTGGTCCAAGGCTCGGGCAAGGGGCTGGAGCCGAAGCGGCCGATCACCCGCGCCGAGACGGCTGCGCTCGTGCAGCGGCTGCTCATCGCCGCCGGCTTGATTGACCAAGCCGGCTCCAAGTAGCAAAAGCAAAAAGGCTGTTCCCCTCGATGCCGGTCATGAAGCCGGATCGTACGGGACAGCCTTTTTTTCGTTTTCCTATCCTCAGCTCGATGCGGCTCGAAGCCGCGCCCGCGAGCGCAGGAAGTACGCGTCCTCGAGCGTCGGCTCCTGGACGGCGAACTCCGGCCCGGGACAGTCCGCTGCGAGCAGGCGCACGCTCCAGAGGTCCAGCTCCGGCCGAACCTGCAGCAGGTCGCCAGGCGGCAGCTCGCGGTAGCGCTCCGGCGAGACCGATCCGCCCCAGACCGAGCCGGGCAGGGCGGACGTCCACTCCTGCGGCGTGCCGTGGAACTGCGGCTTGCCGTCCGCCAGCCACAGGATGCGGGACGCCCAGGCTTCCCACTCGTTGAGCTCATGCGTGGAGACGACGACGGCGCGGCCGCGGGCGTACGAGGCGAGAAAGCGGATCAGCCGCAGCCGCTCGACCGAGTCAAGCGCGTTGAGCGGCTCGTCCAGGAACAGGTAGTCCGGCGAGCCGATGACGGACTGCGCGAGCGCGATCCGCTGGCGGATGCCCTGCGGCAGCGTCTTGATCGCGCGCCGCCGGTAAGGCTCCAGCTGGAACAGCCCGATGACCCGGTCGGTCTCCGCGCGGCCGGCCTCGCCTTTGAGCTCGGACAGATAGCGCAGCAGCCGCTCCATCCGCATGTCCTCGTACAGCTCCAGCCCGGTCGGCACATAGCCGATCGACGAGCGGATCGCCGCCAGATCGCGGTCGCCGCTCATGAGGCCGTAGCGGATGCCGCCCTGGTCGGGAAACTCGGCGGTCGCCAGCAGCTGCAGCAAGGAGGACTTGCCGGAGCCGTTGGCGCCGGCCATGACGGTGATGCCTTCGCGCAGCAGCAGCCGGGGGACGTCCAGCGTGAATACGCCGGCCCGGCGCTCCCAGCGCACGCCGCTCAGCTCGATCATCGGCGGGCCTCCTTTAGACGACCCGCTTGATGACGAGGCTGCGGCGGTACGCCATCGAAATCATGAGCGCGCCGGCTCCAAGGCAGAGCCAGTAGATGGCGGTGCGGATCGTTTCCGGCGCGGAGCTGCCGCTTTCGGGCATGCGCAGCACGTATTCCATGACGTTCCACGCCATCCAGAACAGCGAGCCGATCACGAACGAGCTCTTGACCCCGGCCCGCAGCATGACGTAGGCGGCGCCGCCGGCGATGAGCAGGATGAGCGACATCCACTGAAGGATGAACGGCAGCACCGGGAACTGCTCCATGCGCGTCGCCAGATAGAGCGAGGCCGCCACGCCGAACAGCACGTTCAGGCCGCCGACGATCATGACGCGGGCCATCAGCAGCAGCGCGGGCGGATACGGCGTGATGCTCTCGATCGTGCGCATCTCGCGGTTCCAGCTGCGGAAGCTGTACAGCAGGCCGGAGAGGAACATCATCGGCAGGAACAGCGACAGCTTGGCGCTCACCTCGCTCAGCATTGACGAGCCTTCCTCGCCGGAGCCGTACGGCAGGATGTACATCAGCATGAGGAATACCCCCAGGCTGGCGAGCCAGTACGCCCGCGAATACGCGCCGAGCTGCGTGCGCAGCAGCTTGAGCAGCGTCGGCCGGCGGGCGTCCGGCACGCTGCCGCCCATCCAGTCCGGCACGCCTCGGCCGGAGAGCTCCGGACGCAGCCCGTCGAAGGCGGGCTGCAGCGACGCCAGCAGGCGCGCCGTATCCGAGGCCGTCACCGGCCGCGCGTGCAGCGAGGACAGGGGACCGCGAAGCTCCTCTTCCAGCTGCTTCAGTTCCTTATCGTTCGGCAATTCCATCCGGTTCCCCTCCTTCCGCCCGCATCGGGGCTTTCTGCTCCTTGCCGAGCTTCGTCTTGAGCCGGCGCAGAGCCTTGTACAGATGCGTCTTCACCGAGCCCAGCGGGAGCTGGAGCGCGTCGGCGATGTCCTGCAGCTTGAGATCCTGATAAAAGCGGAGCAGCACGACCTCGCGCTGCACCTGCGGCAGCTCCTCGAGCGTCTGCCGGATCTCGCGGCGCGTCTCCGAGCGCTCGGCCATCTCCACGACGGAGGGCCGCTCGTCCTTGCGCTCCGGCGGCTCGCCGAAGCGGTTGCGGTCGGTCTGGTAGCCGGAGCTTTTCCAATAGTCGCGGCACTGGTTCATCGCCACCCGGTACAGCCACGCCTGCACGTTGTCGGGGCTGCGCCGGTCCTTGAGCTGGCGGATCAGCTTGAGGAACGTCTCCTGCACGATATCCTCCGCCCGCCCCGGATCCTTCAGCTGGCGCTGCAGGAAGCCCGAGAGCGGAGCATGGTAGCGGTGGACCAGCGCCTCGAAGCTCGCCTGGTCTCCGTCCATCATTCCTTGGACCAATTCTTCATCCGTCACCGTCACGCGGTCATCCTCCTTCATCGTCCGTCATCGGCGGCCAGCGGTCGTCCGGCATGCGCGCTCGCCATTCCTTCATAAATTCGTCCACCGTCACGTACGGCGGCGCGGCTGCGGCCATGCGCTCGCCGGCTCCGCTGCGAGGCGGCTCCGGCAGCGCGAGCCCGCGGCTGCGGAACTGCTCCAGCACCTCGCGGGCGAGCGCGGCATGGCCTCGGTCGTAGGCGGCCTGGATCAAGGCGCGCATCGACCTCCATGCCGGCAGCTCCTCCGCCTCGATGCGGTACGGCTCGTCCGGGCCGCGCTGCTTGTTGTACAGAAAAGCATAAGCGGAGCGGATCGCCAAGGCAACGGATTCGCTGCCGGAAGGATCCTCCAGCGCGTTCTCCCGGGCCATCGCTTCTCCCCGACCGACGTCGCCGAACAGCAGCAGGTCGCTCAGCGCGTCCTCGGCGTAGCCGTCGAGATTGCGATGCTCCGTCTGCGGGATGAACAGCGTGTCGTTCTCCGCATGCCAGGAGCGGTTCACGCTCGGAGCCTCGACCGGCGCGCCGATCAGATGCATCGGGAAAAAGAACAGCTGCCGGACCGCGCCGAGCGGAGCTCCGGCCAGCTCCTCCAATCCTTCGCGTCGCCGCTCGAACCGCTCGAGGAACGCTTCCGCCTCGTCCCGGTTGCCCGGCGTCGTCACGATCCGAATCGCCTCGCCCTCCCGCCGGACCGTCTCGAAGCGGCCTCCGACGAGCGTGAGTCCCGCGCCGGAGACGCCGCGGAAGCGGACGGCTCCGTCCGCCGACGGCTCCTCCGGCAGCGTGCCGAACAGCGGAGCGCGGAAGCCGGACGCTTCCACCTCGTAGGCGGTGCCAGGCGTCAGCGCGGACGACGGGCGGTCGAGCAGCCTGCCGTCTTCGTCGAGCGCCAGCAGCGTGTCGCCGCCGGGCAGCGGGTACCAGCCGAGCGAGGCGGGCAGGTAGAGCGCATCGGAGCGGAGGAAGGCGAGATAGCTCTCGCTGCCGCCCGGCCCGCTCAGCCATTCGTCGAGCCGGCCGCCGTAGCGGATCTCCACCGTCTGGACAGGCCGGCCGCGATCGAGCATAAGCTCGGGAAAGCGGATGCTGTCGCCTTTGCGCTCCCAGGCGATCGGCACGCCGTTCAGCTGGACCGACCGCACCTGCAGCGACGGATAGAGCAGCAGCGACACGATGCCGGGCTCCTTGTAGCGCAGCGTCCGCCCCCGCTCGGCCGGCAGCAGCCGGCCCTTTTCGGTCGGCAGCTCGAGCGTCGCCTCGGCGACGAGACTGCCGTCGCCGGCCAGCTTGAGCCGCAGGTCCATCCGTTCCAGCCGGAAGCGGTAGGCGGCGGGATCGAGCCGTTCGTCCGGGCCGGCCGCCGCCTGCTCGAGCTGCGCGCGATGGACGTCGCGGGCCGCCTCCAGCGAGGCGAACGGCGCGAATGCTCCTGCAGCGGCCAGCATCGCCACGAGCGCGAGCAGCCACGGCCGCCGCCGGTTCAGCGGCGGCTTGCTGCGGCCGAGCAGCGCCGCGCCGGCCACGAGCAGGAACAGCGAGAACGCGGCGCCGAAGCCCATGATGCGCAGCAGCTCGCCGCGGGCGAGCGGCCAGGACCAGACCTCGTTGCCGAGCAGGCTGTTCTCGAACAGCGGCTGCAGGTAGAACGCCTTGAGCCAGCTCCATTCGTAGACCGGCCGGATGTAGGCCTGCAGGAACAGCGAGCCGAACACCCAGGCGCAGAACGCCGCCGGCAGCGAGAAGCGGAGCGGCAGCAGCACGCCCAGGAACAGCCCAAGCGCCAGCGAGACGGCGAAGGCATGCTCGTACAGCAGTCCGTAAAGGGCGAGCTGCCGCCCCATCGAGGCGGCGGGCAGGCCGTGCCGCAGCGCCGAGGCGGCGTACGCCGCTCCGACCGCGAGCGTGTACAGCGTCATGTAGGCCAGGCCGGCGAGCCATTTGGCCGCCATCCAGCCGCCGGCGGGCAGCGGCAGCCGGAACAGCCATTCGGCGGACGGATGGAGCAGGTCGCGCCGCATGAGCAGCACGCCGAGCAGCAGCGGGATGGCGGTCGTCAGCATGAGCAGCATCTGATGCGTGTCGGACGCGTACAGATTGATGTCCTGCGACGACTCCGGCCGCAGCCGCCATGTGTGCAGCAGCATCCAGATGGAGGCCGCGGCCGGCAGCAGCAGCGTCCAGCGCAGCAGCAGCAGGGAGCGCAGCTCCATCGCCGCCTGGCGAAGCACGTTCGGAATCATGTCGGACCTCCGGAGGGCTGGCGGTTCATGAGGCTCAGATAGCCTTCCTCCAGCGTCGGCTCCACGCGCTCCGCGAACGGCGACGGCGGGCGGTCGCTCAGCGCGCGGCAGAGGATGCCCTCCTCCGTGCGCCGGGCGCTCAGCAGCCCGCCCAGCGGCATGCGCCGCCATTCGTTCTCCGACGTCTCCCACGCCCAGGTGCGGTCCTCGGCGAAGCCGGCGAGCCCTTGGGTGCTGCCGTGGTACAGCAGCCGTCCTTCGCCGAGCACGATCACCTCGCGGCAGCTCGCGCCGATGTCGCCGAGCACATGCGTCGACAGCAGCACGACCCGCGTCGCCGCGGCCTCGGCGAGCACCCGCCGCAGGCGGATGCGCTCTTCGGGATCGAGGCCGGCGGTCGGCTCGTCGACGATCAGCAGATCGCCGGCCGACAGCAGCGCCTGGGCGACGCCGAGCCTTTTGGTCATGCCGTACGAATAGTGGCGGGCCGGCAGATCGGCCTCGCCGAGCAGATTGACCTGCTCGAGCACCTCGTCGACCTTGCGCCGGCGCTCCGCGAGCGAGCCGCCGCCTTGCAGCGAGGCGGCATGGAGCAGCCACTGGCGGGCGGAGAACTGCGGCAGCACGCGGATGTTCTGCGGCAGGTAGCCGATGCGGCTGCCGCTGCGACGGAAGTCGCGGACCGAGCTGCCGCGCAGCAGCGCGTCGCCGGTCGTCGGCGCCAGCATGCCGGCCAGCAGCCGCAGCAGCGTCGACTTGCCGGCTCCGTTCGGGCCGAGCAGGCCGTGGAGGCCGGGGCCGAGCTCCAGCGTAAGCGGGCGCAGCGCCCAGCCCGTTTTGTATTGTTTTCCCAGCTTGCAGGCGGTAAGCATGTAGATGTGAGCCTCCTGTGCAATCAACGACTGTCTCGCGCAAAAAGTTTCTCTATAGAAAGCAGTATACCATCCGGAGCCGGAGCGCGCCGCCGGCGGAGAACGCCGCGCGGGGGGCGAGGCGTCCTCCGCCGGGCGTCGTTGACAGCTTCGCGACGCGGCGAAGATAATGAAGGAATGTGATCGACGGGCCGGCAGGCGAGGCGGGCGGGAGGCTGCCGCCGCATGCCGACAACGCAGGAGACCGAGCGGAGGGGTAGCCGATGGCGACGGGCAGCGGGCGGGACGAGCAGGAGCGGATGGCGACGGGCAGCGAGCGGGACGAGCGGGAGCGGAAGCCGACGGGAGGCGAGCGGGAGAGGCCGTCCGAAGCGGTCATGAGCGGCGCGGCTGCCGGGCTGCGCAAGCCGCCGCTGCGCTGCGAGCCGGCCGGAGACCGGGCGCTGCTGCTGCTCCCGCCGGGGGACGGCTCGGCGCCGCCGGAGGGCGAGCCGCTGCAGCGGCTGCTGGCCCATGCCGCGGCTTGGCTGGAGGCGGCAGGCTGGGAGTGGCTGGAGGACGCGGTGCCGGCCTATGAGAGCGTGCTGGCCGTCTACGATCCGGCGCGGCTGCAGCGCGGCCGGAAGGGCGCTGTCCCGTGGCGGCTGGCGCAGCGCCTGATCGAGGATCGGCTGGCCGAGCTGCCTCCGCCGCCCGAAGCGGCGGAGCGGGCCGCGATCGAGATCCCGGTGCGCTACGGCGGCGAGCACGGGCCCGATCTGGAGCAGGCGGCGCGGCGCAGCGGCATGACGCCGAGCGCGTTCATCGCGGCGCATTCCAAGCCGCTGTACCGAGTCGTCATGCTCGGCTTCCTGCCTGGCTTTCCCTATCTCGACGGACTGCCGCCGGAGCTGGCGCAGCCCCGGCTCGATGCGCCGCGGCTGCGCGTTCCGGCCGGATCGGTCGGCATCGGCGGCGCGCAGACCGGTCTCTACCCGTCGGAATCTCCGGGCGGCTGGCAGCTGATCGGACGCACCGCTGCGTCGTTGTACGACCCCGCCCGCGAGCGTCCCGCGCTGCTCGCCCCCGGAGACCGGGTGCGGTTCGTTCCGGTGGAGAGATGACATTTGGACGGAATTAGGACCGAATTAGGACAAAAGTCTAAGAAATTATAGGTATTTCTTCATATTTTCGATCTAGATGCCGATAAAAAAACGGCGTCAGAAAGAAAAAGGGGGAGTACCTTATTTTCATTCATAGCAAAACAAGGCCGCGAATAGCGGCCCTGACCGCAGCAGCCGTGCTGCTCGGGTCCGGTTTTCCGGCGCCTCAAGGCGTCCGAGCGCAAGCTTCGGTCGGCGGAACCTATTTCACCGATACGGACAACTGGGGAGGAGGCGCCGCCGGCAGCGCGCCGGACGGCGATCTCGACTACGCGACCAACCGCATCTCCAACGGTCACGCGCTGTACCCGATCGAACTCAAGATCGAGAACGTCGACAAGCTTCCGGCCGAGAGCGCCAGGCTGCTCATACGGGCGTACGATGTCGACGAGTATGACGGGACGGACAGCACTTCGACAGGCGAATGGGATCGGATCTACTTGTCGGACAAGCCGGAGGATATCGTGCTTGGCAATCCCTACACGCCGTGGAAGACGACCGGCGGCTGGAGCAGCGCGACGGCCTCCTACAAGAAAGAGTTCAAGCAATCCGCTTATGTCGGAGCTCTGTCCGGAGCCAACGAGAAGTGGAATACGACGGTGCTGTCGGTCGATCCGGACAGGATCAAGCTGGGCGACCAGTATGTCGGCGCATCCATCCACCACTACTTCAAGTCGAGCAGGCTGAACGCCGGCTGGGTGACCGAGATCGACTGGGCGCAGCTCGTCGTGGACGGCGGCATCCGGGACAAGGCGGAATTTTCGAGCGCCGGCATCACGGTCAAGAACGGGAAAATCTCGATTGATTCGGCTTTTCTGGGCAAGGCCGGATACCAGGGCCCGTTCTCGCTCGAAGCCAACGTCATCCAAGAGGTCACGGATGCGGACGGGACGGTGCGCGAGGTCAACCTCGCTCTCGACAGCAAGCGGGTCGCCAGCGTGGATCCGGGCGAGCCGGGCCGCTGGAGCCTTGATCTCGAGAACCCGGACATCCGTCTCGGCGAGGACTATCGGATCAACTTGATCCTGTTCGAGGATCGCGGAGGCAACGGATCGAACCCGAATCCGGGCAAGGTGCAGCATCTGCTCGATATCCCGACCTCGGAAATCCAGATGCTGGCGGAGGACTTCCGCAAGCCGTCGTCCGTCTTCGCGGCGGAGGACTTCCGTTCCAGCTTCTTCAAGACGAACGGCGTCGAGGGCGCTGACGCCTTGGCCAACGGAGCCAATCTGGAAAAGATCCGCATCGCGTCGCTCCCCGATCCGCAGGACGGCGAGCTGATGTACGACGGCGTTCCGCTGAGCGCCGCCGATATCGGCAAGGAGATCGCGATCGCGAACGTCTCCAAGCTCGGATTCCGTCCGGCCTCCACCACCGACGGGGAAGCCGAATTCGGCTGGACCGGCTTTGCCGAGGGCAAATATGCCTCCAAGCCGGGCCAAGCGAGCTTCGGCGTCAACCGCGCTCCGATCGTGGAGTCGCTGAGCAAGCCGGCGCTGAAGGGCGAGACGCTTTCCTTCAGCCGGACCGACTTCGCGCAGGCATCCGCTTATGTGGATCCGGAGCAGCAGCCGCTGGCCGCCATCATGGTGACACAGCTGCCGGATCCGGCCAAGGGCAAGCTGTACCTCAAGCGTGCCGATGCGCCGCTTGTGCCGATCGTCGCAGGCATGCCGATCGCCGCAGCCGATCTGGACCGCCTCGTGTTCCAGCCGGAGGCCGGCGCGACGGGCACGGCCGAATTCCGCTGGAACGGAAGCGACGGCGAGCTGTACGCCGCAGCGGACAAAACCGTCCACATCCGGATCAACACGCCGCCTGTCGGCGCCGATCTGAGCCGGACAGGGCCGATGGGAGCGCCGATCGGCTTCGCGGCTCCGGGCGGAGGGAGCAGCTTCGCGGCGCTGTACGGCGACGAGGACGGCGACGCCTTCCATAGCGCCGCGTTCGACCTGCCTGCCGGCTTCGCGGCGAAAGGCACGCTCAGCTATACGGACCCGTCCACGACGGAAACCGTATACGCCGAGCCCGGCCGGCGCACGCTGGTGCCCGCGCTGGCGCTGGAATCGCTTCGCTTCGTGCCGGCGCCAGGCCTCGCCAACGGCGCGGCGGTCGACATCCCGTGGCGTCCGTTCGACGGCAAGCAGCTGGCGGAGCAGCCTTCGCTGCTGCGGATCGCCTACGACGGCATTCCAAGGGCGGAATGGATTTTCGCCTTGGCCAATGAAGGGGTCCAGGAGCTCCGCCTGATTCCGTCCGGGACCGACCAGGAGACGGTGACCGGCCTCGTCTACCGGCTTGTTCCGGATTCTGGCCCTTCCCGCGGAACGCTCGTTCCGGACGTGGATTCGGACCGGGGCGGCTGGATCTACACGCCGGACAAAAGCTTCGTCGGCGGCACGGACAGCTTCCGTTACGTCGCGGTGGATGAGAGCGGACAGGTCAGCGAGCCTGCGACGGCGACGATCATCATCCACAAGGCGCTCGACGGCTGGGCGGGAGACAAGCCGCAAGGCGATCCGAGCCGCATGACGGCGCTGCCGGGCTACCCGGTCCGGCTGTCCGCGGTATCGTCGCTGGCTGCGGAAAAAGTAACGGCATCGCTCGCAGGAGCGGAGACCGAGCTGGTCTGGATCAATCCGTCGACGAGCCAGGCGGAAGGGGTCAAGCGGTGGGAGAAGGAGGGCTTCCTGCTGCCGCAAGCCGCGGCAGGCGAGCATGAGGCGGCATTCACCGCTTACGGTCCGCTTGGACAGCTGATCTCAAACGAAGAAGCCTCGCGCCGATCGGACAACTGGATCACCGTGCTGACGACCCGCATCGCCTTGACCGCGGATCCCGACCGGATCGTCGGCGACGGCAGCTCGACTTCCGTGCTGACCGCAGCCGTGACGGACGAGAGTGGCGGTCCGGTGAGCGGCGTATCCGTCTCGTTCGCGGCCGGAGCCGGTTCGTTCCCGGACGGCGCGACTGCCGTGACCGGAGCGGACGGCAAGGCCAGCGTCGTCTATCGTTCGGCGGCGATGAGCGGCACGGCGGAGCAGCGGATCCCGGTTACGGCCAAGGTGCTGGATCTCGTACGAGGGTTGGCCGGAGAAAAAGGGATCGAGCTGACGTTCCTGCCTGCCCGCATTCAAGGCGTCCTTACCTCCGGCAGCTCCAATGCGCCGGTCGCAGGAGCGATCGTCCGGGCGGCGCTGGATCTGAACGGCGACGGCGTCATCGAGCCTGGCGTCGATTTTGAAGCCTCGACGACGACGGATGAGCGTGGACGCTATTCGCTGGCAGTGCCTAAGGGAGACGCGGTCTACGAGCTGGCGGTTACGCAGCTCATCGAGATCGGCGGCGTGCCGACTCCGGTCACCTATACGCAAAAAGCCGTTGTCGGCCATGCCGACGGAACGGGGGAGCAATCCTTCGAATCCGAAAAGACGGTCAGCGGCATCGTTCTGCTCAAGCAGCCGGACGGCGGCACGGCGAAGCTGGATGCGGAGACGGCCGGCCGTTCCAGCGTTTATTTCAAGGACAGCCAAGGAAAATACGTCACGGACGGCAGCGGGGCGCCGAAGGCTCATCCGCTGAGCGCCCAGGGCGTCTTCTCGACAGAGGGCCTGCCGGTCGGCTCGTACGCCTTCGAGATCCGGTATGAGTTCGAGCCCGGCGTGCAGGCGGTGCTGAGCGTAGGCCAGGCTCATGTCAAAGCGGACGGAGAGCTCAACCTGCTCACGCAGCTGGTCGATCCGTACGGAACGGTAAGCGACGCCTCGAGCGGAGCCGTCATCGAAGGCGCGACGGTCATGCTGCATTACGCCGACACCGGCCGCAACAAGGCCGCCGGCAAGGCTGCCGGGTCGGGCGTCGTCCTGCCCGCGCTGGTCGGCTTCGAGCCGAACGACAACGCCAGTCCGTTGCAGATGACCGACAAGAACGGGTTCTACGCGTACATGGTCTACCCGGAGACGGACTATTATCTCGTCGTCTCCAAGGCCGGCTACGAGACGTACCGCAGTCCGGTCATATCGGTCGAATGGGACATCGTCAAGCATGACCTTCAGCTGCGCCCGCTGTCTGCGCCGGCTCCGCAGCCTCCGGCACGGACCGGACTGGCGGTGGAGATCGCCTCGGAGCAGATGGTCGTGCGCGAGGAGAGCGAGTCGCTGCTGACGGTCACCTACAAAAACAGCGGTTCCGACCGCATGGCAAGCGGAACCGTCGAGGTCGTCCTGCCTGACGGCGCAAGCTTCGTCCGCGCCGACGGCGCGGCCATCGAGGGCGCGAAGGCGGTCTGGAGCGTCAAGGATCTCGCAGCCGGACAGACGGGCCAGCTGCAGCTGACCGTGCGCTGGCCGCGCCTGGATGCGAAGGAAAAGGACGCCGACATCACCGCGGCCTTCTTCTCGGGAGATGCGTCCGCGAAGTCGGTCGCCAAATTCAAGCTGTACTCGGACCGCTTCGAGCCGCTGTTCCATTCGCGCTACATCCGCGGCTAACCGGACGGGGAGTTCAAGCCCGGACAGACGCTGACGCGGGCGGAGGTCGCCGCTGTCACGGCGCGCTTGTCCGACGGTCCGGCCGATGATGCGAAGGCGGGCTCCTTCCGCGACATCCGCAGCGGCCACTGGGCGGAAGGCTACATCCGCGAGTCTGCCGCCAAAGGCTACTTCAAGGGAGGAACGGACGGCCGCTTCCGGCCGGACGCGCCTGTGACCCGCGCGGAGCTCGTCGTCGTCCTGTCGCGCTTCCTCGGCCTCGAGCCGGGAGAGCCTGCAGGCAGCCGCTTCCTCGACACGGCCGGCCACTGGGCCGAAAAGGAGATCGAGGCGCTGCGCGTCGGCAAGTATTTGAACGGCTACCCGGACGGAAGCTTCCGTCCGAACCAGCCGATCCGGCGCGACGAGGCGGTCGCTCTCATCAACGGCATGCTGCGGCGCGGTCCGCTTGCCGGCGTGCAGCCGCTGTTCCCGGACATGCCGCAGGGCAACTGGGCTTACGGAGCTGTCATGGAGGCTTCGCTCTCTCATGAATCGGAGCGGGTCGAGGACGGATCGGAGCGCCTGCTGAAGGCGATCGAGGACCATATGGAATAACGAAAAAGCGAGGCTCAATCAGCCTCGCTTCGGAAAGCGGCATCGGGCCCGAGAGGCGCCCGGCGCCGCTTTTTTTCATGCCGCTCGGCGATGGCGTCCCGTGGCGGCGGCCGATGGCCGCGGGAAGGCGGCAACGGAAAGCGAGCAGCGGATGACTGTCGTCGGCATGAGCGGCTTCCGCCGCTTAGCAGCCTCCTTCAGCCTTCTTCAAAGCGGCCGAGCGCGATGACGGCATTATGGCCGCCGAAGCCGAACGAGTTGGACAGCCCGACCGCTAGCCTCTCGCGCCGCGGGGCGGCCGGGACGGTCAAGGCGCAGTCCGGGTCGGGCTCCTCCTGGTTGAGCGTCGGCGCGATCAGCCCCTCGCGCAGCATGCGGACGAGCGTGATCGCCTGCGCGCCGCCTGATGCGCCGAGCATATGGCCGGTCATCGACTTGCCGGCGAATACCGGCACGCTCCCGCCTCGCTCGCCGAGCGCGCTGCGGATCGCCCGGCTCTCCGACAGGTCGCCGGCCGGCGTGCCGGTCGCATGGGCGCAGACGAGGTCCACGCGCTCGGCCTCCAGGCCGGCGTCGGCGAGCGCCAGCCGCATGGCGGCCGCCGCGCCGCGGCCGGTCGGCTCGGTCGCGACCCGGTGGTACGCGTCGGAGGTCGCGCCGTAGCCGAGCACCTCGGCCAGCGGCTCGGCGCCGCGCGCAAGCGCGTGGGCGAGCGTCTCGAGCACGATGATGCCGGCGCCCTCGGCCATGACGAAGCCGGAGCGGCTGCGGCTGAAAGGACGGCTGGCCGCCGCCGGATCGCCGCCCGACGAAGCGAGCGCGGTCGCGTTGCCGAAGCCGGCGAGGGCGATCGGGACGACGGCGGCTTCGGATCCGCCGGCGACGGAGACATCGGCGATGCCGGCGCGCAGCAGGCGCATCGCTTCCCCGATCGCCGTGTTGCCGATCGAGCAGGCGGTCACCGGCGAGAGCGTCGGCCCGGTCAGGCTGTAGCGGATGCTGATTTCCGCGGCGGCCATGTTGGCGATCATCATCGGCACGAGCGTCGGGCTGACGCGGCTATGGCCGCGGGCGCCCAGCACGCGCGCCTGCTCCATGAGCGTGCCGAGCCCGCCGATGCCGGAGCCGACATAAACGGCCGTCCGATCCGGCACGAGCCGGCCCTCGCCGAGTCCGGCCTGGCCGAGCGCTTCCTCGGCCGCCGCGAGCGCGAACTGCACGAAGCGGTCCATCTTGCGGGCTTCTTTGCGGCCGAACCGGGCTTCTCCGTCCCAATCGGGCACGAGGCCGGCAATCGCCCGCTCGTCGGCCTGCTCCAGCCACTCCTCCGGCCATCCGCCTTCTTGCAGGCGGCGGATGCCCGAGCGGCCTTCTGCCTGGGCGGTCCATAACGTCTCGGCGCCGGCGCCGAACGGACTGACGGCTCCCATGCCGGTAATGACGACGCGATGCTCCTTGCTGGACGGGGCGGCGTTCGTGTAAAGCTCCATCATGCTCCATCTCCTTCGCAGCTTGCGGATAAGCGCAGTTTCGCACAGCTCTTATGCTGGTACAAGTTGTTGTTTATACTAGGATAAGAAGTAATGGGATCGAGGAGGAAGGGCATGAACCGACAGGAGAGGCTGAAGGCTCTATCGGAATTTCTGCGCTCGCGCCGGATGGCGCTGCTGCCGGAGGAGCACGGCTTTCCCGCAGGGGGGAGGCGGCGGACGCCGGGGCTGCGGAGGGAGGAGGTCGCGCAGCTGGCCGGTGTGAGCCCGACCTGGTACACCTGGCTCGAGCAAGGACGGGACATCCGCGTCTCGTCCTCGGTGCTCGACGCGGTGGCGAAGGCGCTGCGGCTGAATGCGGACGAAAAGCGGTACATGGCCGCGCTGGCGGGCGACGCCGCAGAGGGCGGCGAGCCGGAGAGGAGCGCGTCCGACGAGCCGGCGGCGCTGCCCGCTCCGCTGGGGCGGATTTTGGACGAGCTGGCCGGCTGTCCCGCGATCGTCTCGGATCGCCGCTGCCGGATCGCCGGCTGGAACGAGGCGGCGGCCCGCGTTTTTCTCGACTTCGGCTCGGTGCCCACGGAGGAGCGCAACATGATCACGCTGCTGTTCACCCGGCCGGAGCTGCAGCGGCTCGCCGTCAACTGGGAGCAGTTCGTACGGGGCTATCTGGCGCTGTTCCGCTATTACTACGGCCGGTATGCCGACGACGACTGGTATTCCCGCTTCATCGAGGCGATGGAGCGGCGCGACGCCCGCTTCGCCCCGCTCTGGGAGGAGAGCCGCGTCAGCGCCGCGCCGGAGGTGATCCTGGAGTTCCGCCACGCCCGCGCGGGCAAGATGCAGTTCCAGCTGACGAGCCTGCAGGCCCAGGGACAGCCGGATCTGCGCGTCAGCATCTACACGCCCGCTCAAGGCACGGCGACGGAGCGCAAGATGAGACGGCTGATGGACGAGGAGCGGGGCGGCTGAGCGGAAGATGAGGCGGCTGATGGACGAGGAGCGGGCGGCTGAGCGGAAGATGAGGCGACTGATGGACGAGGAGCAGGGCGGCTGAGCGGAAGATGAGGCGGCTGATGGACGAGGAGCGGGCGGCTGGGCAGAAGATGAGGCGGCTGATGGACGAGGAGCGGGGCGGCTGAGCGGCAGGCGGAGCCGCGAGCGGAGGGAATGGAAGTCTGTCGTGGCTTCATGCGGACAGGCCAGCCGAAGCGCTTCAGCGGAACGGGCTGCCGGCCAAGCAGCTGGTCGCGGGGCCAGTCGATGAGGTCGAGGCGCGGGATGGCAAGCTGGAGCCGGCATGAGCTACAATGAAGGTCATGAGCGCGGAAAGGAAGGGATGAGGATGAGGACGAAGGAAGCGGCGTTCACGATCATCCGCCCCGGCTTCGGCGCCGAGCTGCAGCATCTGGGCCGTCCCGGCCTGCGAGCCCAGGGCATGCCGGCCGGCGGCGCGATGGATGCGGTCTCGCTGCAGACAGCCAATCTGCTGTGCGGCAATTCGCGCGGCGCGCCGGCGCTGGAGCTGGCGCTCGGCGGCGTCCGCATGCGCGTCGACGCGCCGGACGGCGTGCTCGCGGCGATTTGCGGCGCCGACATGCCGGCCGACTTGGACGGCGTGCCGGTGCCTGCGGGCCGAGCCGTCTGGCTGCCGGCGGGCGGCACGCTTTCGCTCGGCGCGGCGCGCTCCGGCTGCCGCGCCTACTTGGCCGCCGCAGGCGGCCTCGCCGCGCCGGGGCGGCGGCCTGTGGCGCGGCCGGCGGCGATGAACGCGCCGGCATCGGCCGCCGGCTTGCCGCCGGCGAGGCGCTCCGCCGCGGCGAGCCTTCGGCGCGCGGCGCGGCGCTGCTGGCGGCGCTCGCGCAGCGCGCCGCCCAGGCCGGCGGCGGCGGGAGGCTGCCCGCCGCCGCGCCGTGGCTCGCGCCGCGCCTCGTGGCGCGCGGCGGAGCCGACGGCTCCGGCACCGCCGTGCTGCGCGCGGTGCCGGGAGCCGCTTACGGGCAGCTGACGCAGGCTGCCCGGGAGCGGCTGTGGCGGGAGCGGCTCGCCGCCTCTCCCGCCAGCGATCGGATGGGCGTCCGGCTCATCCCGGACGCCCATCCGATCGAGCTCGAGCGCCGCGCGGAGCTGCGCTCGCACGGCGTGCTGCCGGGCGCGGTGCAGCTCCCGCCCGGCGGCCATCCCGTCGCGCTGGCGGCAGGCTGCCAGACGACGGGCGGTTATCCCGTCATCCTGCATGTCATCGCCGCCGACCTGCCGCGGCTCGGCCAGCTGCGGCCCGGCGACGGGACGCGCTTCCTCCGCGTGGAGCTGGAGGAGGCGCAGCGCCTCCTGCTGCGGCAGCAGCGGGAGCTCGACCGGCTCGAAGCCGCGCTGCGGCTTCGGACCGAACGCTTCTTGCAGGAGCAGCGCCGCGCGCCGGCCGCTGACAGCTGATTTTTTCATTTGAACAGGAGGTAAGCGACATGACCAACGATCAGCCGGGCGTCGACCCGCAGGCTGCGAGCAGCGCCAAGTCCGGCAAGCGGAAAGGGGCGCCGGCCTTCGTGGCCGGCCTGTATACGGCCGATGCGCCGGGCAGCTTCGTCTCCCGCGAACTTGCGGAGGCAGAGCTGGAGTTCGGCGGAATCCGCGGCGACCGCCACTTCGGCGTGACGTCCCGCGCGGACAGCCGCCAGCCAATGTATCCTCGCGGCACCGAGATCCTCAACCGTCGGCAGATCAGCATCCTCTCGCGCGAGGAGCTGGAGGAGACGCGGGAGCGGATGGGCATCGAGGCGCTCGATCCCGAGTGGATCGGCGGCAACCTGCTGCTCTCCGGCTATCCCGGGCTGACGCAGCTGCCCGCAGGCTCGCGGCTGCTCTTCCCAAGCGGCGCCGGGCTCGTCTGCGAAGGCGAGAACCATCCCTGCACCGACGCCGGCAAGGAGGTCGAGCGGCATGTCGCTCCCAAGGAGCGGCTGCCGCAGGCGTTCGTGAAGGCCGCGCGCGGCCGGCGCGGCATCGTCTGCTCCGTGGAGCGTCCCGGCCGCATCGCGTTCGGCGACGAGATCCGCATCATCCCCCCGATGTAGGGGAAAAGGAGGCCATCCCGCATGCAAAAGCCGACGATCGACCTGAACGCCGATTTCGGCGAAGGGTATGGAAGCTACGCCTTCGGAGATGACGCCGCGCTGCTCGGCTCCATCACGAGCGCCAGCATCGCCTGCGGCTGGCATGCCGGCGACGCCCGCACGATGCGGACGTCGGTCGAGCGCTGCCTGCGGGCCGGCGTGGCGGTCGGCGCCCATCCGGGCTACCCGGACCGGCAAGGCTTCGGCCGCCGCGCGATGGCGCTGGACGCCGAGGAGGTGTACGAGGCCGTCCTTTATCAGACGGGCGCGCTGCAGGCGTTCGTGCGCGCCGCTGGCGGCGAGCTGCGCCACATCAAGCCGCATGGCGCGATGTATCATCGCTGCGGAGCCAGCCAGGCCCATGCGGATGCGGTCGCCCGGGCTGCCGCCGAACTGGGCGGGCTGGCGCTGTTCGGCCCTCCCGGCGGACTGCTGGAGCGCGCGGCCGTCTCGGCCGGACTGCCGTTCGCGGCGGAAGGCTTCGCCGACCGCGCCTACTTGCCGGACGGCTCGCTCGCCGGCAGGGACCGGCCCGGCGCCGTGCACGGCGAGCCGTCCCAAGCGCTGGAGCAGGCGCTGACGATCGCGCTGCGCGGCGAGGCGCCCGCCTTGGGCGGAGGCTTCGCGCCGGTGGCGGCTCGGACGCTGTGCCTGCACGGCGACGGACCGGGCGCGGCCGAGCTGGCCGCGCTTATCCGCGCCGGCCTGGAGGCGGCCGGCGTCGCCGTGCGCGCGCCTTGGCAGCCATGAGCGGCGTGCTGGAGGCTCGCCGCAGCCGCTCCAGCTCCGAGGCCAGGGGCTCGAAAGCCCTTCTCGGAGCAAGCCCCGAAGCCGGCGGCTCGGAAGCTCCTCTTGGCGCATGCTCCGAGGCCGGCGGCTTGGAACCTCCTCTTGGTGCATGCTCCGAGGCGAGCGGCTCGGAAGCACCTCTCGGCGCATGCTCCGAAGCCGGCGGCTTGAAAGCCCTTTTCAACGCATGCCCTGAGGCCAGCGGCTTGGAAGCCACTCTCGGCACATGCTCCGAGGTCAGCGGCTCGAAAGCACCTCTCGACGCTTGCTCCGAGGCCGGCGGCTCGGAAGCCACTCTCGGGGCATGCCCCGAGGCCGGCGGCTCGAAGGCACATCGCCCCGCATGCCCTGTGAGCAACGATCCGCAAGCCGCTCGCGGCCCATCCGCTCCATCCGCTCCGCTGCCTCAGGCTGATCAAGCACATTCGTTGATGTCCCCATCCTCTGGCATCTGGATGTTTGTCTACGGTACGCTACAGCCCGGACGCAGCAACTTCGGCGTCGTCGCTCCGTTCGTCCTTGCGCAGCGGCCGGGACGGGTGCGGGGGCGCCTCGTCGACGCGGCGGACGGCCATTATCCCGCGCTTGTCCGCGAGCTTTCCGCTTTGAACCGGGCCGTTCGGGGCTGGTGGCTGCTGCTGGAGCGCGACGGCTTGGCCGCCTGCGATCGGCTGGAGGAATTTTTCGGCCCGGAAGAGGCGAATGACTACGAGCGGATCTGGACGCGGGATCTCGACGATCCGGCCCGTCAGGGCTGGGTCTATGTCTGGCCCGACGACCGCGGCTGCGCCGATTTGCACAACGGAGTGTGGCCGTAACGTTGCAGTCTCGTTTGCAGCCTCGAGTTGAGATGGAAGCGGGCTTGGCTCCACCACCAGCATCGTACACCCTGAGACAAAAGCGGAGCTTGAGCGGCTGACGGCTATGAATAAGGATAGAAACCAAACCGCTGGTGACGAGGCGGTTTGGTTTTTGGTTTTCCCAACTATCGGAATACTGCATTCTAGCTTGGTTATCGGGCGTTCGGAGCCTGGCTCTCCGGCTCGGGTTCGAAAGCGATCAGCGTCACCGGGCGGCCTTCTCCGTCCGACAGCGATTGCTCCAGCTCCCGGATCCTTTCCACTGCCACGAGGGGAAGCTCGGCGTATCGGTACGGCTCGAAGGGCTGGGACTTGCTCATCTGCGTTCACCTCCTTGCGGATAGCGTTCGCTCTCCACAGCATCTTTATCCAGATAAAGGGAGAGGGGGGCGGCGCTTTTGAGAGGCGTCCGCTCCATCACATCGACGCTCATCGCTCGATCGTCCGTCACGGGATCGCTCGAAAAACTCGGATTGCAGCTGCCCGGCGGCGCGCATCCGAGACCGTAACCGGAAAAAGTCGGGCTGCAGCTCCTGGGCAGAGTGCATCCGAGCCTCTAACCCGAAAAAATCGGGTTGCAGGCGCCAGGCAGAGCGCATCCGAGGCTGTAACCCGAAAAAATCGGGTTGCAGCCGTCTGGCAGAGTGTATCCGAGCCTGTAACCCGAAAAAATCGGGTTGCAGTCACCAGGGCAGAGCGTATCCGAGCCTGTAACTCGAAAAACTCGGGTTGCAGGGCTTTGAGGTGCGCGTTCGTAGGCAATTACGCGGAAAAACCGAGTAACTCGGGCGTGCAGGAGGAGAAACGGAGGGAGTTGCGCGGAAAGACCGAGTAACTCGGGCATGCAGAAGGCGAAGCGTAGGGAGTTGCGCGGAAAAACCGAGTAACTCGAGCATGCAGGAGGAGAAACGGAGGGAGTTGCGCGGAAAAACCGAGTAACTCGGGCGTGCAGGGGAAGACACGGAGGGAGTTGCGCGGAAAAACCGAGTAACTCGGGCGTGCAGGGGAAGACACGGAGGGAGTTGCGCGGAAAAACCGAGTAACTCGGGCGTGCAGGAGGAGAAACGGAGGGAGTTGCGCGGAAAAACCGAGTAACTCGGGTGCGAGGATGGCAGAACGCCCGGAATTGCCGGGCCTTCCCCAAATGTTCACAAACCGGATTGGTCGAGATGGAGCCCATCAAGTAAACTAGAGGGCGAGAGGAAGGAACGAAAGGAAGTGCCCCCGAGCGCATGAACGCCAACTCACGCAACGAATTCCCACCGGACGCCATACGAGCGGCAACGGCGCGGAAGCAGTCTCAAACCTCGCACGAGACCGAGCTCGCCGCAAAGCGGCCTCGGCCAGAGGCGCTCCATCGGCCTCGCGCCTCGGCGCCGCGCCCCCCGGCGCCCGGCCACCGCGCCTCGGCTCTGCGCCCTCTGGCGCCCGGCCACCGCGCCTCGGCTTCGCGCCCCCCGGCGGCCGGCCCCCGCGCCTCGGCGCCGCGCCCCGGCGGCCGGCCACCGCGCCTCGGCTTCGCGCCCTCTGGCGCCCGGCCACCGCGCCTCGGCGCCGCGCCCCGGCGCCTGGCCACCGCGCCTCGGCGCCGCGCCCCGGCGGCCGGCCACCGCGCTTCGGCGCCGCGCCCCGGCGCCTGGCCACCGCGCCTCGGCTCCGCGCCCCCGGCGGCCGGCCTTCGCGCCTCGGCGCCGCGCCCCGGCGGCCGGCCACCGCGCCTCGGCTCCGCGCCCCTGGCGGCCGGCCACCGCGCCTCGGCTTCGCGCCCCGGCGCCCGGCCACCGCGCCTCGGCTTCGCACCCCCCGGCGCCCGGCCACCGCGCCTCGGCTTCGCGCCCCCTGGAGCCCGGCCACCGCGCCTCGGCTCCGCGCCCCCTGGCGGCCGGCCACCGCGCCGCAGCCGCCGCCAAGCGGCCGCGGCCAGCTTCGCACCGGCGGCCCGGCGCCTCCCCGCGCGCCGCGCGCCTGACGCTGCGGCGCCTCAACGCCGCGCTGCTCGGCGTGCTGGCGCTGCTCGCGCTGCTGCTCGGCGCGCCGCAGCAGGCAGCGGCGCACGCGTCGCTGCTCGAAGCGAGCCCGGCAGCGGGCTCGCGGCTCGAAGCCGCGCCCGCCGAGGTGCGGCTCGTGTTCAACGAGCGCATCGAAGGCGCGGTCGGCGCGCTCGAGGTGCTGGACGGCAGCTCCGATCCCGTCACCGCCGAGCGGGCGAAGCTCAGCGAGGACGGGCTGACGCTGACCTTGCCGCTGCCCAAGCTGGGCGAGGGCGTCTATACGGTAAGCTACCGCATCATTTCCGAGGACGGCCATCCGGTCGGCGGCTCCTACGTCTTCGTCGTCGGAGACCCGCCCGCCGCGCGGGACGCCTCGACGTTCGACGTCCATGCCCAGCTCGGCCACGCCGGCCACGAAGAAGGCGGGCTGACGACGGCCAGCCTGATCCTGTACGCCGTGCGCTTCCTGTACTACGCGGCGCTCATGCTGGCCGCCGGAGCGGCGCTCTGGCCGCTGCTGTACCGGCAAGGCTGGTCCCGCATCCCCGAGCCGCTGCGCGGACGGCTCGAGCGGCTGCCGCAGCAGGCGCTCGTGCTCGCCGCGCTGCTCTACGTCTTCGTCGAGACGCAGCAGCTCATGATCGGCCAGCCGGCGTCCGAATGGAGCCGGCTGTTCACGGCTACGGCCGTCGGACAGAGCTATCTGGCGCTGCTGCTGCTCGCCTTTGCCGGCCTCGCGCTGCCGGCGGGCCGAAGCGCGCTGCGCTTCGTCTGGGCGCTGCCGCTGCTCGCGACGGAGGCGTGGAGCGGCCATGCGGCCGCTGCCGCGCCGCGCTGGGCGGCGCTCTCGCTCGATTACGTCCATCTCGCCTTCGCGGCGCTGTGGGCGGGCGGCCTCATGCTGCTGCTCGTCCTCTGGCAGGCGGAGCGCAAGGAAGCCGGACGCTTCGCCGCCAGCTTCTCGCGCATGGCCTGGATCAGCATCGTGGCGCTGACGCTGACGGGCATCGGCTTGACGCTCCTGTACATGACCAAGCCCGAGTATTTGCTGCTGACGCCTTGGGGCATCCTGCTGCTTGTCAAGACCGGGCTGGTCGTGCTCGTGGCGGGAGCCGGCTTCCTGATCCGCGTCCGCATGAAGCGGTCTGGCTTCCCGGGCGGCGCGCTGCTCAAGGCCGACGGCGCGCTGATGGCGCTCATCCTCGTCATCGTCGGCATTTTCACCTACATCAGCCCGCTTCCGGCCAACGAGCCGGTCGGCTGGCACAAGATGGGCAGCGAGATGCATGTGTCGATCCGGATCGCGCCGAACGTGCCGGGAGACAACGAGTTCACGGTCCGCATCTGGATGCACAAGAGCCTGGGCGATCCGAAGTCGGTCCAGCTGCGCCTCATGTCCGAAGACAAGCCGGAGCTCGGCGCGATCGAGATTCCGCTGGAGCCGTTCAAGGACGACGAGATCAGCACGTTCGAAGGCTACACCAAGACGGCCTACCGGGCCAAGGGCACGTATCTTCCGTTCGCGGGCCGCTGGACGGCCGAGGTCCGCGTCATGGACCCGAACGACGACGAGCGGGTCGAGCGCTTGAGCTTCCGCAATTACTGACGAGCGGCGACAGGAGCTGCGAGAGGAGCCGGCAGGCCGGCCGAGGAGGGGGAGACGGACGAGATGAAAGCAAGCACGATCAAAAGGCTCATCCTCTGGACGCCGACCGTCCTGACGGCGGCATGGGAATATGCCCGCCATACGTTCCTGTTGCCGTACGTGTCGATGGACACGGGCAACGTCATCAGTCCGATCCTCGTTTTTCTCGTCACGGTGACGCTGCTCTCCAAGCTGTTCGCCATGCTTGAGAACGTGCAGGAGCAGCTGCGGCGCGAGCAGGCGGTGAAGGCGGCCGTCCAGGAAAGGGATCAGATGGCCCGCGAGCTGCACGACGGCATCTCGCAGTCGCTGTTCCTGCTGTCGGTCAAGCTCGATCGGCTCGACCGGGCGGAGTCGCCCGAGGAGGTCAAGCAGGCGAGCGAGCAGATCCGCGGCACGGTGCGCCATGTGTACGAGGACGTGCGGGAGGCGATCGCCAGCCTGCGCTCGGCGGATACGGCGGCGGAGAGCGGCATGCCGTGGCTGCAGCCGCTGCAGGATGCCGCGGCCGAGCTGGAGGAGTCGGGGACGAGCACGGAGATCGACTGGCAGCTGCCCGACCTGCTGCTGACGAGCCGCGAAAAGGTCGAGCTGCTCGCGATCGTGCGCGAGGCGCTCATGAACGTGCGCAAGCATGCCTCCGCCTCGCTCGTGAGCGTCGCCTGCCGGCAGGTCGGAGCGGACGGCTTTCGCTGCGTCGTCGCCGACGACGGGCTCGGCGCTTCGCCGGGAGCCGAGTCGGCCAAGGGCCATTACGGCGTGCGCATGATGCGCGACCGCGCGGAAGGCGCGGGCTGGAGCTTCCGGTTCCAGAGCCCCCGCCCCGACCTGGAGACAGGCACGTCCGTCGAAATCATGCGCCAGCCGTCTGACGCCAAGTTGAAGCCATGAACATCGAGGAGGAAAGACGATGAATGCTGCCGAACGGAACGACCCGGTGCGGGTGCTGCTGGTCGACGACCATCCGCATGGGCGCGAAGGAATGAGGATGATCGTCTCGGAGGACCCTTTCTTCGAGATCGCCGGAGAGGCGTCGGGAGGGGAGGAGGCGGTCGCGCGCGCCGAAGAGCTGCAGCCGGACCTCATCCTGATGGACATCCGCATGCCGGGCGTCGGAGGGCTGGAGGCGACGTCCCGCATCAAGGCGTCGCTGCCGTCCGTCAAGATCGTCATGGTGACGGTGTCCGACGATATCGCCGACCTGTTCGAGGCGATCAAGCGGGGAGCCCAGGGCTATCTGCTCAAAAACCTGTCCCCGTCCGCCTGGCTCGATTACTTGCGGGCCGTCTCGCTCGACCAGGCGCCGATGAGCCGGGAGCTGGCGACGCGCATCCTGCAGGAATTCCTGCCGGGAGGGCGGGCCTCCGCGTCCGCGGACCCGCGGACGGCGATCCCTTCCGCTCCGCGGACGGCGGCGTCGACGCTGTCTCCGCTCACCGAGCGCGAGAAGGAGATCCTCGAGCGCGTCGCGCGCGGCGACTCCAATCGCGAGGCGGCGGCTGCGCTCGGCATTTCGGAGAATACGGTCAAGAACCATCTCAAGAACATCCTGCAGAAGCTGCATCTCGACAACCGGGTCCAGCTCGCGCGCTACGCCTACGAGAACGGGCTCATGGACCGCGGCGCAGGCGGAGGCTGAGTCGGCGAGAGGGCGGTCCGCACGGCGGCCGGTCCCACCTTCCCGAGCGGACGGCGGACCGGCCGTCGTCCTCATTTTTGTCAAGATCATAGCCCTTTCGGGTCATGTCCATTGCCTGCGGCGATCCTATACTTGTAAAAGAAAATCACGGACCAGCACAACAGTCCGACAGGAGGAAACAAGACATGAATCAACGCCGCAAAAGCGCGCTGTCCCGCAGCAAAGGGAGCGTCGCGGCTCTGCTCGCCGCGCTGTCGCTGTTCCTGATGGCCGGCATGGCGAGCGCCCATGTGACGGTATGGCCCAAGGAGGTCGCTCAGAACTCGTATGAGGTGTTCACGGTGCGGGTGCCGAGCGAGAAGAAGGACGTGCTGACGACCGCGGTCGCCGTGCGCGTGCCGGAGGGCGTGAACATCACCCGCACGCAGCCGCAGCCTGGCTGGAAGACCGAGCTCGAGCGCTCGGCCGACGGCAAGATCGAGCGCATCACCTGGACGGCGGAAGAAGGCCAGGGACTGGCCGTCGAGAACTTTACCGAGTTCAAGCTGTCGGGCAAGGTAGAGGCGGACGCGACCGAGCTCAAGTGGAAGGCTTACCAGACGTACAGCGACAGCAGCGTCGTCGAGTGGATCGGCGCGCCGGACGCCGACTATCCGGGTCCGGTCACGGCCGTAGGCGCCGGCGAGGCCGAGAGCGACGGCCATGGCCACGGCGCGGCCGAAGCGAGCCCGGCTCCGAGCTCGGCTCCAGACGCATCGGCTGCTCCGGAGGCGTCCGCCGCTCCGGCCGCCAGCGACGCCCCGGCTGTCGATCAGCCGCTTGCTCCGGCTGCGGAGAAGGACAGCCTGCCGCTGATCCTCTCGATCATCGCGCTGGCGCTCGGCGTCGTCGCCGTCATCGCGGCGTTCACGCGCCGCGGCGGCTCGAAGGGCTGAGCAGGCGGCCGAGCCGCCTGCGCCCCCGCATGGCTTCTGCCACCAGAACCCCGGACGGATCGAGCCTCTCGATTCGTCCGGGGCCATTTTTGCCCATCGTATAGGGGAGAAGGAAGGATGCCGCTGATGAAGGAAACGGAACAGGCGCCGCTGCCGCAAGGGACGGCCGGGCCCGGCCGCGCGGCCTTGCCTGCCGAATCGTCCGCCGGGCCTGAAGCGGCGGCTGCCGATGCCGGGCGGACGGAGCCCCTTCAGTTGCATTTTCTATTCGCTCTGGATATAATGAGCCAAGATATCCACCAGCATCGATGGAGACCAGTACGCCATGCCTGGCCCGACAGGGAGGGACCGCCGCCGATTGAGAGCGGTCCCCGGCAGCCAGCCGGCCGAATTCACTCCGGAGCTCGAGCCTTGAACGCGTCCGCCAGGACGCCTGTAGAGGCTCGCGGGCAGCCGTCCGTTATCCGGCCTTCAAGCAGCCCGGCGCATCCGCGCCAGGGACGAGCGGCTTTTCCGGCGGGTTTTCCGCCTCCAGGAGATGCCCCGCCCAGCGGCTGGAATCAGGGTGGTACCACGGTCCTTTCGTCCCTAGCGGAGAAAGGGCCTTTTTGTTTTTTCACAGCGGCTTGCGGCGGCAGCCGGAGCCAAGTCCGAAGGAGGCGTTAGCGATGAAGGAACGTTTGGAGGCTTTGCAGGCGGAAGCGCTGCAGGAGCTGCAAGGAGTCGCCGGACCGCAGGAGCTCGGCGAGCTTCGCATCAAGTATTTGGGCAAAAAGGGCGCGCTCACCGAAATTCTGCGCGGCATGGGCGCGCTGAACGCCGAGGAGCGTCCGGCCGTCGGCGAGGTCGCCAACCGCGTGCGCGGGGCGATCGAGGCCGTCATCGAGGAAAAGGCGGCGGCCTACCGGCGCGCCGAGACCGAGCTGCGGCTGCGCTCGGAGACGATCGACGTGACGCTGCCCGGCAGCGCGCTGCCGACCGGAGCGGTCCATCCGCTGAACAAGGTCGCGCAGGAGATCGAGGACATCTTCATCGGCCTCGGCTACACGATCGCCGAAGGTCCCGAGGTCGAGACCGACTACTACAACTTCGAGGCGCTCAACCTGCCCAAGAACCACCCGGCCCGCGACATGCAGGACTCGTTCTACATCACCGACGAGATCCTCATGCGCACGCAGACGTCGCCCGTGCAGATCCGCGCCATGAAGGCGATGAACGGCAAGTCGCCGCTCAAGGTCATCTGCCCCGGCAAGGTGTACCGCCGCGACGACGACGACGCGACGCATTCGTTCCAGTTCAACCAGGTCGAGGGACTCGTCGTCGGCAAAGGCATCCGCATGAGCGACCTGAAGGGCACGCTGCTGCAGTTCGTGCAGGAGATGTTCGGCAAGCAGGCGCGCATCCGCCTGCGCCCGAGCTTCTTCCCGTTCACCGAGCCGAGCGCCGAGGTCGACGTCACCTGCTCGCAGTGCGGTGGCAGCGGCTGCCGGATGTGCAAGCAGACCGGCTGGCTCGAGATTCTCGGCTGCGGCATGGTGCATCCCAAGGTGCTCGAGGCTGGCGGATACGATCCGGAGGAAGTGACCGGCTTCGCCTTCGGCATGGGCATCGAGCGGATCGCGCTGCTCAAATACGGCATCGACGACATCCGCCACTTCTACGCGAACGACCTGCGCTTCCTGAGCCAGTTCGAGCGGATGTAAGGAAAGAGAGGGGACTAGCGCCATGAAAATATCGACGAACTGGCTGGCGGACTACATCAGCCTTGAAGGGCTGACGCCGCAGGAGATCGCGGAGAAGATGACGTCCGGCGGCATCGAGATCGACGCCGTCGAGGCGATGGATAAAGGCGTAAGCGGCGTTGTCGTCGGCTACGTCAAGGAAAAGACGAAGCATCCCGACGCCGACAAGCTGAACGTCTGCAAGGTCGACGTCGGTGCCGGCGAGGACCTGCAGATCGTCTGCGGCGCGGCCAACGTGGACGCCGGCCAGCATGTGCCGGTCGCGACCGTCGGCGCGAAGCTGCCGGGCGGCCTCGCGATCAAGCGCGCCAAGCTGCGCGGCGTCGAGTCGCAGGGCATGATCTGCTCCGCCCGCGAGCTCGGGCTGAACGACAAGCTGCTGCCCAAGGAACTGCAGGAGGGCATCCTCGTCCTGCCGAAGCTGGAGCTCGGCCGGCCGATCGTCGACGTGCTCGACCTCGGCGCCCATGTGCTGGAGCTCGATCTGACGCCGAACCGCTCGGACGCGCTCAGCTACCTCGGCGTCGCCTACGAGATCGGCGCGCTCACGGGCCGTCCGGTCAAGCTGCCGGAGAGCGCCGTGTTCGGCGCGGCGGACAAGACGGCGGACCGCCTGTCCGTGCGCATCGACGCCCGCGAGGCTTGCGCGCACTACAGCGCCCGCTACATCCGCGGCGTGCAGGTCGCGCCGTCGCCGCTCTGGCTGCAGAACCGGCTGATGGCGGCCGGCATCCGGCCGATCAACAACATCGTCGACGTGACGAACTACGTCATGCTGGAATACGGCCAGCCGCTCCATGCGTTCGACGCGGACCGCGTGGCCGGTGGCAGCATCGTCGTGCGCTTCGCCCGCGAAGGCGAGGAGCTGGAGACGCTGGACGGCCAGCTGCGCAAGCTGCAGCCGCATATGCTCGTCATCGCCGACGGCGATCGGGCGATCGGCCTTGCCGGCGTCATGGGCGGCGCGAACTCCGAGGTGGACGGCGATACGACGAACGTCATCCTCGAATCCGCCAAGTTCGACGGCTCCGTCGTGCGGCGCACGTCCCGCCAGCTCGGCTTGCGCTCGGAGGCGAGCCTGCGCTTCGAGAAGGAAGTCGATCCGGCGCGCGTCATCCCGGCGCTCGACCGCGCGGCTTCGCTGATCGCGAAGCTCGGCAGCGGCCTCGTCACCGACGGCATCGCCGAGGACGTGGCGCGCACGTACGAGCCGGCCGTCATCGAGGTGTCGCTGGAGCGGATCTCCGGCTATCTCGGCGCGGACATCTCCAAGCTGGAGGCGCAGGCGATCTTCGGCCGCCTCGGCTTCGACTCCGAGGTCGGCGACGGGTCGATCCGTGTGGAGGTGCCGACGCGCCGCGGGGACATCTCCCGCGACGTCGACCTGATCGAGGAGATCGCCCGCCTGTACGGCTACGACAACATCAAGGCGACGCCGATCGTCGGCGAGACGACGCCGGGCTCGCTGACCGCGCCGCAGGCGGTGCGCCGCGAGCTGCGCCGCCGCTTGTCGGACGCCGGCCTGCACGAGGTCATCAGCTACTCGTTCACGGCGCCGGAGCGGGCGGGGCTGTTCCCGGACCTCGCTCAGGACGCGAAGCCGATCCGCCTGGCGATGCCGATGAGCGAGGAGCGCAGCGTGCTGCGCACGTCGCTGCTGCCGCAGCTGCTGGAGACGGCGGCGTACAACCGCAATCGCAAAAACCACGATCTCGCGCTGTTCGAGATCGGCACGGTGTTCCACACCGACGAGGAGACGCTGACGCGTCTGCCGCAGGAGAAGCATCGCTTCGCGCTGCTGCTGACCGGAGCGAGCCGCTCCGCCGCGTGGAACCGCAAGGCGGAGAAGGCCGACTTCTACGACGCCAAGGGCGTGCTGGAGACGATCTTCGCCGCGCTCGGCCTGAGCGGATCGGTCTCCTACGAGGCCGCCGCTCCGTCCGGCCTGCATCCGGGCCGCACGGCCGCCGTCAAGCTGGACGGCGAGCGCGGAGCGGAGACGATCGGCTACGTCGGCCAGCTTCATCCGGAGCTGCAGCTGGAGCTCGGCCTTGACGACGTCTTCGTCGCCGAGCTGGAGCTGGGCGCGCTGTACGATGCGGCCGACCGCTCGATCGTCTACCGCACGCTGCCGCGCTATCCGGCGGCCGACCGCGACATCGCGGTGACGGTCGACGAGACGGTGCCGGCGGCCGCGCTGGCCGCCGCTGTCCGCGAGGCGGCCGGCGAGCTGCTGGAGTCGGTGCGGGTGTTCGACGTCTACACCGGAGAAAAGCTCGGCGCCGGCCGCAAGAGCGTCGCGCTGGCGCTCGTGTACCGCCATGCGGAGCGCACGCTGACCGACGAGGAGGTCGCGGCGGCGCATGCCGCGGCGGTCGCCGCGCTGGAGCAATCTTTCTCCGCGGAATTAAGGAAATAGGCAGGAAACGCAGGAAGCCGCATCGAAGTAATCCCGCGAGGGAGCTGCCGATGCGGCTTTTCCTTGTCTGGAGGGGCGCGGCGAAGCCGGAAGGCCCTCTGGATCGTTCTTATCCACATGGATCTTGACGCCCTGAGACGGGCGATCGAAATAGACGGGCAGCAGGAGAGCAGCTCAACGAGCAACGGGAGGATACCGCCTTGAAGGAAGCCGATCGCTTGAGAGTAACGGTCGATATATACGGACATCAATACCGGTTGACGGGTCATAGCAGCTCGGATTATATCCGCCGGGTCGCGCAGGTCGTCGACGAGAACATGCACAAGCTGGCCAAGGGCTACCCGCGGCTGGACATGCCGAGGCTGGCGGTGCTTGCGGCCGTGCATATGGCGGAGGACGTATTCCGCTTGCGGCAGGACAGCGAGCTGCTCAAGGAGGAGCAGAGCATCCGCAAGACGCTCATGGGCGAGCTGGACAAGGCGCAGGCCGCGACGGAGCAGGCGCGCGAGGAGCTCGCGCGGTCCGAGCGGCGGGCGGCGGAGGAGCTGGAGCGGCTGCTCGGCGAGCGCGAGGCGGCGGAAGCCGCGCTGCGCGCCGAGGCCGAGGAGCGGCTGGCCGCCGTGCAGGAGGCCGTCAAGGAGGAGGCGCAGCGGCTGGAGCGCCAAAGCGCCGAGACGGCGGCCGAGCTCGAGCGGCGCTGGCGGGAGGAAAGAGAGCGCCTGATCGAGGAGAACCGCGTCCGCGCCGAGGAGCTGGAGCGCCGGCATGAGGCGGAGCGCGCCGAGGCCGCGCAGATGCTGGAAGCGGAGCGGCAGGAGTGGGAACGGCTCTACGAGGCGGAGGCGAACGAGCGCGAGTCGCGGCTTGCCGAGGCGATGGCGGAGGCGGAGCGGCGCCATGAGGCGGAAAAGGCCGCCGCCCGCGAGCAGCTCGAGACGGAGCGGCGCCGGCTGGCGGTGCAGCTGGAGGAGAGCCGCGCGGAGCTGGAGCGCCGGCTCGAGGAGGAGCGCGCCGAGGCGGCCGGCGTCTTCGAGCGCGAGCGGGCGGAGCTCGCGGCGGCGCATGCGGCCGAGATGGCCGCGCGCGAGGAAGCGTTCGCCGTCCAGCTCGCGGAGCTGGAGGAGCGCTTGCTGGAGCGCATCCATGAGCTTCAGGCGCTGCATGCCGGCGAGGCCGAGGCGCGCGAGCGCGAGCGGGCGGAGCTGGAGCAGCTGTACGAGGCCGAGTGCCGGGAGCGCGAGCAGGAACGCGCGGCGCTGCTGGAATCGAAGCGGGCGGAGCTCGAGACGCTCGAGGCTCGTCATCTGCTGCGCGTCGGCGAGCTGGAGGAGCAGCTGCTCGCGGCGCGGCAGCAGGGCGAGCGCAGCCTCGCCGAGCTTCGCCTGCAGCAGCGGGCGGAGCTCGAGGGCGCGCTTGCCGGCCGCGAGGCCGAGCATCGCGGCGAGCTGGAGCGGCTGCGCGCGGAGCAGGAGCTTCAGCTCGCCGAAGCGCTGGAGCTGGCGCAGGCGACGGAGGCTGAGCTCCAGTCGCAGCTGACGGAGAGCGCTTCCGCGCTGGAGGAGGCTCGCCTGCAGCTCGCCGCGCTGGAGCAGCGGCTGCAGCAGCAGCGCCAGGAGCAGCAGCGGCAGCTGCAAGAGCTGCAGCAGGAGCAGCTGCAAGTGCTGCAGGAGCTGCGCCAGGAGCAGCAGCAGGCGCTGGAGGCCGAGCGGCAGCAGCTGCAGGAGCGCCAGCAGGAGCTGGAGGCCGAGCAGCAGCAGCTGCAGGCCGAGCGCGAGCGCGGCAGCCGGCTTGAGCTGAAGCTTGCCGCCGAGCGGACCGGACGCGAGGAGGCGGAGCGGCTGTTCGCCGAGGCCGGAGAGCGGGCCGAGGCGCTGGAGCGCGGCGAGGCCGAAGCGCGCGAGCGGCTCGGCCTTGCCGAGGAGCAGCTCGAGGCGTCGCGCCGCGAGCTGGAGGCGCAGGCCGGCCGCGCCGCCGCGCTGGAGGCGGAGCTGGAGCGGCTGCGCGCGGCGTCCGCCGCCGAGCGCGAGGCGGCCGCGAGCGAGCTGCGCGAGGCGCTGGAGCGGGCGGCCGGCGAGATCGGCCATGCGCGCGAGCAGGCGCAGGCCGAGGCGGCCGAGCAGGTGCGCGCGGCCGAGCGGCGCGCGGAGGCGCTGCAGGCGTCCGCCGCCGAGGAGGCGGAGCGGCTGCGCCGCGAGGCGGGCGAGGAGCTGGAGCTCGCGCAGCTTGCCGCGCAGGAGGAGCGCGAGCGGCTCGCCGCCGCCCATGCGCAGGAGCGCGAGCGGCTCGCTGCCGCCCATGCGCAGGAGCTGGAGCGGCTTCGCGCTGCAGCCGAGGCCGAGCGCATCGGCGGCGCGGAGCGTCTGCGCGAGCTGGAGGAGCGAGCGGCCGGCGAGGCCGGCCGGGCGGAGGAGGCGCAGAGCCGCCTCGCCGGGCAGGGCGAGCAGTGGGCCCGGGAGCGGTCCGGCCTGGAGCAGGAGCGCGACGCCGCCCGTCGCGAGCTGGCTGAGGCTCGCGACGACTGGTCCAAGCGGATCGCGGATGCCGAGGAGCATCTGATGCTCGTCATGGAGCAGGAGGAAGCCCGCGGCCGGCTGCTCGGAGAATCCCAGCGGCTGCTGCGCTCGACGCAGGAGGAGCTGGAGCTGTCCCGGCAGCGGACGGCGGAGCTGGATGACCGGCTGCGCGAGACGGCGAGCCGCCTGCAGGAAGCGGTCGCTTCCCGCGATGAGGCCGAGGCCGCCCTGCGGGAGCGGCTGGCCGCAGCCGAGGCTGCCCGGGAAGCGCTGGAGCGCCGCCTGTCCGAGATGACAGGCCAGGCCGAGGCGCTGCGCGAGCAGTCCGAGCGGGACTGGCAGCGGCAGCTGGACGAGGCGGCCGCCGAGCGCGAGCGCCTGAGCCGTCTTGTCGCCGAGCAGCAGGAGCGGCTCGAGCAGCAGTCCCGGCTGGAGGCGGACCGCGCCGAGGCCGAGGAGGAGCTGCGGCGCCAGCTGGAGCTCGCGCATCGGGAGGCCGCCGTCTCCGGCAGCGCGGTCGAGCGTCTGGAGGATGCGATGCGTCAGCTGGAGGAGGAGCGCACGGACAGCCGGCAGGATCTCGGCGAGCTGCAGCGCGACAACGAGCGGCTGACGACGGCCTACGACAAGCTGCGCACGGAATTCGAGCTGCTGCGTACCGAATATTCCAAGCTGCAGACGGAATATAACGAATGGATCGAGCTGATCGAGCAGAGCTGACGCCTTGAAGCGTGTCCGTCTCGAGCGGTCAAAAGAGGAGCCTTGCGGGCCGGAAACGGCATCCCGCAAGGCTTTTTCATTTCCCACAGGCGCAGTTGGAATAGAAAAGTCCCCCGGTGCCCAAGCACTTTTCTCCCTGTCGCCGCTTCCCTATATCCTCTAGTATTTAGGTGAAATAGACAATTTTAGCTCTTTGACAATGAGGAGAATCAGGAGATTGGACCTAGGGCTGCGGGCAGCCTTGCCTCGCTTGTTCCCGTGCCTTGCGGCATGCCGGTCCTTTTCTCCTGCAGCGCGTCCCCGCGGCGCGCGCCGCATCTTCGCTCATTCCCCCCACCACGACTTCCTTCGAGCCGTTTCGCCGGCGAGCTTCCATCCACTCTTGACGAAAGGCGGTGCCCTCGCTCCTGCGGCCTCCGGCCGCGCTGCGTCCGAACTCCCGAACCGATCGCTACCATTCCCAAGAGGAGAGTGTCCTTATGTTCAGAGAAATCCACAAATCCAAAATCCACCGCGCCGCCGTCACCGAGGCGAACCTCCACTATGTCGGCAGCATCACGATCGACCAGGACCTGCTCGATGCGACCGACATCTGGGAAAACGAAAAGGTGCAGGTCGTCAACATCAACAACGGCTCCCGCCTCGAAACCTACGTCATCCCCGGCCCGAGGGGCTCCGGCGTCATCTGCCTGAACGGCGCCGCCGCTCGGCACGCGCAGCCCGGCGACCTCGTCATCATCATGTCCTACGCGATGATGGCCGAGGAGGAAGCCCGCGGCTACGTCCCCAAGGTCATCGTCCTCGACGCGGACAACCGGATCGCGTCCGCCTCCTACCGCGAGCTCCATTCCACGACGATCTAGCGGAGGACGACATCATGGACTCCTTCCTCACGCTGACCGGGCTGCTCGCCGCGAGAAGGCGCGATGCGTCCGGCATCGTCTTCGCCGAGCCGTCCGGCGAACGATTCCTCCCCTATGCCGAGCTGGAGAGCCGCGCGCTCGGCTGTCTCGTCTCCCTTCGCCGCCGCGGGCTGCGGCCCGGCCGGCATGTCGTGCTTCAGACCGAAAGCAACGCAAGCTTCCTGGAGCTGTTCTGGGCCAGCCTGCTCGGAGGCGCCGTGCCGGTGCCGCTCGCGGCGGCGCGGACGGACGAGCAGCGCCGCAAGCTGGCGGCCGTGCTCGCCCAGCTGCCCGCTCCGCTCGTGCTTGCCGATGCCGATCTCGCCGAGGCGGCGGGCGGCGCGGACGTGATCCAGATCGCGGAGCTGGAGCCGGCGGCGGACGGGGGGACGACTCAGCCGCATCGAGCCGATCCGGACGAGCCCGCGTTCATCCAATTCACCTCGGGATCGACAGGCGATCCGAAAGGAGTCGTGCTGACGCACGCCAACCTGCTCGCCAACATGCGGGGCATCGTCGACGGAGCCCGTTCCGGGCCGGGAGATTCCTCGCTCAGCTGGCTCCCTCTGACGCATGACATGGGCCTCATCGGCTTCCATCTGTCGCCGCTGCTGGCCGGCATGACCCAGTGGCTGATGCCGACGTCGCAGTTCGTGCTGCGGCCGATGAGCTGGCTGGAGCTCGCTTCCCGCGAGCGGATCACCTGCCTCGCCTCGCCGAACTTCGGCCTCCTTCATCTGCTCCAGCATTTCAAGCCGGAGCAGGCGACGGGCTGGAATCTGTCCGCCGTGCGGCTGCTGTTCAACGGAGCCGAGCCGATCTCGGCGGACGCCTGCCGCTCGTTCCTGGAGCGGCTCGCGCCTTACGGGCTGCGGCCGCAAGCTCTCTTTCCCGTCTACGGCCTCGCCGAGGCGTGCCTGGCGGTCACCTTCCCCGACCCGGACGAGCGGCTGCGCACGGTCCATGTCCGGCGCGGACGGCTGCGTCCCGGAGAGCCGGTGCCTTTCGCGGCGGCCGGCGATCCGCAGGCGATGGAGCTCGTGGAGCTCGGCTCGTCCGTCGCCGGCTGCGAGGCCGCGCTGTTCGACGAGCTGGGCCGCAGGCTTGGCGAGGACGAGGCCGGCCTCGTCTGCATCCGCGGCCTCAACGTGACGGGAGGCTACTACAACCGTCCGGACGTCAACGAAGCGCTGATCCGGGACGGCTGGCTGAACACCGGCGACATCGGCTTCTTCCACGGAGGGCGGCTCTATCTGACCGGACGGGTGAAGGACATCCTGCTCGTCAACGGCCAGAACTATTATCCGCATGATCTGGAGGAGCTGCTGGCCGAGCTGCCGGCATGCGCAGCGGGCAAGGCGGCGGTCTGCGCCGTCGCCGACCCGGCATCCGGCTCCGAGGCCGCGGCGGTATTCGTGCAGCATCGCGGCAAGCCGGAGTCGTTTCTGGACATCCGCCGCAGCGTGCGCGTCCTGCTGAGCCGCCGGGCCGGACTTGAAGCCGGCCCCGTCATTCCGGTCAAGCGCATCCCCAAGACGACCTCGGGCAAAATCAAGCGCTTCGAGCTGGCGGACGAGCTGCTCGCCGGCCGCTTCGACGAGGCGCTCGCCGCGCTGGAGGCGGCGGAGGCGGCAGCGCTTGCGGCTGCGGCGGCGGATATGCCCTCCGCAGCGGCGGATGCGTCTTCCGCAGCGGCGGATGCGTCCCTCGCAGTGGCGGATGCGTCCCTCGCAGCGGCGGATGCGTCCCCTGCGAAGGGGGCGCCGCCGTCCGCGTCAGCGGAGACGGCCGCGGAAGAGGAGCGGCCCGCTCCGGCGATAGGCGCCGGCGCAGGCGAGCCGCGCGGAGAGACGGGCAAGCAGCCGCCAAGCCTGTCGCAGGAGGAGACGGCGACAGAGCGCCGGCTGCTCGCGATCTGGCGGGAGCTGCTCGGCACGGAGCGGCTCGGCCGGGACGATTCCTTTCTCGAGCATGGAGGCAATTCGCTGCGCGCTGCCCTTGCGGCGGCCCGCATCCAGGAGGAGCTGGAGACGCCGCTGCCGCTGACGGAGCTGCTCCGGCACGATACGGCTCGCTCGCTGGCGGCCTTTATCGAGGAACGCAAGGCGGAGGGGGCGCGGATCGAACCGCCGGCCGAGCCGATCCGGAGGCGGATGCGCGCCGGCTATCCCGCAACGCCTGCGCAGCGGCGGCTGCATGTGCACGAGCAGCTGTACCCGGGCTCGCTCAGCTATCAGCTGCCGTACGAGATCGCTGTCGACGGCCCGCTCGACGATGACCGGCTGCGGCGCGCCTGGCAGGAGCTGCTCGCCCGTCATGACGCGCTGCGCACCTCGTTCCGCGTCGCGGAGGACGGCGTCCTCGTCGCCGAGATCGCGGACCGCGCGGAGCTGCCGCTTGCGACCGTCGACCTGACGGGGCTCGCGCCGCAGGAGGCCGAGGCGGCCGCGGCTGAGCGGGCGCGGGCCTTTCCCCGGCCGATGGAGCTGGAGCGGGCGCCGCTGCTGCGGCTGGAGCTGCTGCTCCTGCCGGAGGGGCGCCGCCGGCTGCTGCTCGACCTGCATCATCTCGTGACGGACGGCAGCTCGATGGGCGTGCTCATGCAGGAGCTGGCCGCCCTGTACGATGGCCGGCCGCTGCCGGAGCCGGCTCCGGGCATCGGCGACATCGCCGAGCGGGAGCGCGAGGAGGAGGGCGGCGCGGCTGCCGAGCGGTCGCGGCGCTACTGGCGGGACCGGTTCTTGTCCGGCGTGCCCGCCGCCGCTTTTCCGGCGGATCGGCTCCGCCCGGCACGGCCGACCTTCCGCGGACGGTCGGAGCGGCTCGCGCTCGGTCCGGAGCTTACGGACGGCCTCGGCCGGCTCGCGCGCCGCGCCGGGACGACGCTGTACGGCGCGCTGCTCGCCGTCTACGGCGTGCTGCTCGAGCGGTACGCGGGCGAAGACGACGCCGTCGTCGGCACGGCGTACGCCCGCCGCACCCGCCGCGAGACGGTCGGCACCGTCGGCCTGCTGGCGACGCTGCTGCCGCTGCGGCTGACCGGCAGCAGGGAGAGCAGCGTGCTGGACTGGGTGCGGACGGCCGGTGAAGCGGCCGCCGAAGCGATCGAGCACGGAGCGATCGGCTACGAGGCGATCGTCGAGGCCGTCGGAGCGGCTCGCGAGCCGGGCCGCGCGGCGCTGTTCGATACGGCGTTCACGCTCCAGAACGTGGAGCTGCCGGAGTTCCGCACGGAGGAGCTGGCGCTGCGGCCTGCGATGATCGAGACCGGCTCCTGCAAGTTCGATCTGTTCTGGGAATGCGAGCTCGGTCCGGAAGGGCTGTCGATCCGGCTGGAATATGCGGAGGACTTGTTCGACGGCGAGACGGCCCGGCAGCTGCTCCGCCATTACGCGCAGCTGGCCCGCGAGGCGGCGCTCGATCCGCTGCGCCCCGCCGCTTCTCTCCCTTTGATGGACGAGGAGGAGCGCGCGCTGCTGCTGCGGCGCGGCCTCAGCCGCTGGCCGGAAAAAGACGCCGTCCCGCTGCAGGAGCGGATCGGCCGGCACGCGCTGGCGTCGCCGGAGCGCATCGCCGTCTCGTTCGCAGGCGGCAGCTGGACGTACGGCCGGCTGTGGGAAGCTTCCGGACGCGTCGCGGCGGCTCTCTCCGCGCTCGGCCTCGGCCGCGGCTCCCGCATCGCGATCGCGATGGGCCGCTCGCCGCAGCAGCTGGCGGCGCTGCTCGCCAGCCTGCGGATCGGAGGCGCGTACGTGCCGATCGATCCGGGCTATCCGGCGGAGCGCGCGGCATTCATGCTGGCCGACGCCGAGGCCGACATCCTGCTGGCCGACGAAGCCGCGCTCCCGCTGTGCCGGCAGGCGATCGCCGCCTGCGGACGTGCGGTGCGGCTGATCGAGGCCGAGACGTTGGCCGGGCGCTGTCCGTCCAGCTCTTCGCCCGACTCGCCGCTGCCGCGCACGGCTTCCGCCGGCCCGGCCGGGGAAGCCGCGGAGCGCGCGGAGAGCTTCGTTTCGCCCGACGATCTGGCCTACATCCTCTACACCTCCGGCTCGACCGGCAGGCCGAAAGGAATTCGTACGACCCACCGCAACGTCGCGCGCGTCGTCGATCGGCCGGGCTATGTGGAGATCGGTCAGGACGACGTGCTGCTGCAGCTGTCGAGCTATGCGTTCGACGGCTCGACGTTCGACATCTATGGGGCGCTGACGAACGGGGCGAGGCTCGTGCTTGCAGGCAGCGACGAGGCGATGGACGCTCCGGCGCTCGTCCGGCGGCTGCGGGAAGAAGGCGTGACGGTGCTGTTCGCCACGACGGCGCTGTTCAACACGCTGGCGGCCTACGGCCTGGACGGGCTGCCGCGGCTGCGCAAGCTGCTGTTCGGAGGCGAGCGGGCTTCCGTCTCCCATGCGCTCAAGGCGCTTGCCGCGCTCGGCCCGGATTCGCTGCTGCATGTGTACGGGCCGACGGAAACGACCGTGTTCGCCACCGCCTGGCCGGTCCGGCCGCCGGCGCCGGGAGCGGCCTCGCTGCCGATCGGCTGGCCGGTCGACGGCACGGAGGCGCTCGTGCTCGACGCTTGCGGACGGCTCGCGCCCGATCTCGTTCCCGGCGAGCTGCATGTGGCAGGCGGCGGCGTAGCGGCCGGTTATGTCGGGCTGCCGCGCGAGACGGAGGCGCGGTTCATGCCGCATCCTTTCCGCGCCGGCGAGCGCATGTACCGGACCGGCGACCTCGTGCGGCGGCTCCGGGACGGCAGCCTCGAGTTCCTCGACCGGCTCGACCAGCAGGTCAAGCTGCGCGGCTTCCGCATCGAGCTCGGCGAGATCGAGGCGAGGCTGCTGGCAAGCGGACAGGCGGAGGAGGCTTATGTCGGCCTCGTCGGCGAGCCTCCCCGGGCGGAGCTGTGCGCCTATGTCGTCGCCGCGCCGGAGCGCTTCGACGCGGCATCGCTTCGCCGCTGGATGGCGGGCGGGCTGCCGCCGTTCATGCTGCCGGCCCATCTCGTCCGTCTGGATCGCCTGCCGCTCGGCCCGACCGGCAAGGTCGACCGCAAGGCGCTGCCGCTGCCGCAGCCGGGCGATGCGGCGGGCTCGGCGGGCGCCGAGCGCGAGCGGCCGGCGACGGCGAGCGAGCGCGAGCTTGCGGAGCTGTGGCGGGAGGCGCTGGGCCGGGCCGATGTCGGCGTTTTGGATTCCTTTTTCGAGCTTGGAGGGCACTCGCTCACTGCAGCCGCGCTGACCGGCTTGATCCATCGCCGGCTCGGCGTCCGGATGCCGGTGCGGGAAGTATTCGCCCGCCCGACGATCCGCGAGCAGGCCACTTGGCTCGACAAAGCCGAGCGCTCCGGCAGGGAGCCGCTGCTTCCGGCGGCGCCGGCGGAGAGCTACCCGCTCCATCCCGCCCAGGCGCGGCTCGCGCTGCTGGAGCGGCAGGGCGGCATCGGTCTCGCCTACCATGTGCCGCTGGCGCTTCGGCTCGTCGGATCGCCCGGCCCCGAAGCGGTGCTCGCCGCGCTGCAGGCGCTCGTCGACCGTCATGAGCCGCTGCGCACCGAGGTGCGGGATGCCGGCGGCGAGCCGCGCGCGTTCGTGCTGGCGCAGGCGGAGGTCCGGCTGGAGCGCATGCGGATCGCCGGAGAGGAAGCTCTGCCGGGGGCGATGAAGTCATTTCTCCGTCCGCTGCCGCTGGACGCCGCGCCGCCGCTTGCGGCCTGTTATGCCGAAGGCGGTCAGGGCGAAAGCTTCCTGCTGCTGAACCTGCATCATCTCGCGGTGGACGGCGTGTCCGTCGGCCTGCTGCTGGAGGAGCTCGTCCGCCTCCTGGAGGGCGGCCTGCCCGAGCCCGCGCCGACGGTCCAATTCAAGGACTACGCCGCCTGGTTGGACGCCGGCTTCGCACGCTCTGAAGCGAGCGTCGACTCGCCGGACGCCGGCGGCTCCGCGCGCTCCGAGGCGAGCGTCGACTTGCCGGACGCCGGCGGCTCCGCGCGCTCCGAGGCGAGCGGCGACTTGCCGGACGCCGGCAGCTCCGCGCGCTCCGAAGCGAGCGCCGCCTGGTGGCGCGAGCAGCTCGCGGCTCCGTTGCCGCAGCCGGAGCTGCCGCTCGACCGGCCGCGCGGGGCGAGCCGCTCCTTCGAGGGCGGGCTGCTGGCGTTCGATTTTCCCGAGGGGCTGACGGACGGCCTCGAAGCGCTCGCGGCGCGCTGCGGCGTGACGCTGAACAGCCTGCTGTTCACGCTGTACGGCGCACTGCTCGCCCGCTGGACCGGGGCGGAGGAGCTGATGATCGGCGCGCTCGGCGCCGGCCGCTCCCATCCCGACACCGGCTCGATGATCGGCATGTTCAACTCGTTCCTGCCGATCCGGGTCGCGCTGCCGCGCGGGCTGCCGCTGGAGCGGGCGGCCCGGGACGTCCAGGAGCGGCTGCTGTCCGCGATCGAGCATCAGGAGCTGCCGCTGGAGCGGCTGCTCGAGCTCGCGGGCGGCCCGTTCGATCCGGCCCGCAATCCGCTTTTCGACACGATGCTCGTCCTGCACAGCCAGTTCGGCGGCGAGCTGGCGGTCCGCGGCAGCCGCTGCGCGCTGGAGCCGGTGCGCTGGGGCGGCGCCGGCACGGCCAAGCTCGATCTCAAGCTCGACCTGTACGGCGACGGTCCGCACGGGCTGCGCGGCGAGCTGGAGTACGCGGCGGCGCTGCTTCAGCCGCAGACGGTCCGGCGCCTGGCCGAGACGTGGATCGAGCTGCTGCAGCGGGCGGTCCGCGAGCCGCATGCCGAGCTCGGCGTCCTCATGCGGCTGACCGGCTCGGAAGCGCGGCTGCTGGAACAGTGGAACGCGACGACGGCCGCGTACCCGGATCGAAGCACGCTGCACGGCCTGTTCGCCGAGCAGGCGCGGAGAAGCCCGGACCGTCCCGCGGTCCGCTCCGCCGAAGGCGTCTGGACGTACCGCGAGCTCGACCGCGTCTCCTCCCGCATCGCCGTCCGCCTGCGGGCTGCCGGCGCCGGCCGGGACGCGATCGTGGCCGTTGCGGCGCGCCGCTCGCTGGCGATGATGGCCGGCCTGCTCGCCGTGCTGAAGGCCGGGGCCGCCTACTTGCCGATCGACCCGGACCAGCCGCCGGAGCGGCTGCGCGACATCGCGGACGACAGCGGCTGCGGGCTGCTGCTCGCCTCGCGAGGCGCCTGCATGGAGCTGGCGGACGCGGAGCCGAGGCGGCTGCGGCTGGAGCTGGAGACGCTCGTCGCGGAGGCGCTGGCCGCGGAGGCGTCCGCGCCGGGCGAGCTCCTGCCGGAGCTCGACGCTGCGGCCGAGGCATCGCCCGAATCGCTCGCCTACGTCATCTACACGTCCGGCTCGACCGGGCGCCCCAAGGGCGTGCTGATCGAGCACCGGGCGATCGTCAACCGGCTGAGCTGGATGCAGCGCGCCTATCCGCTGACGGAGGACGACGTCATCCTGCACAAGACGCCAGCCACCTTCGACGTATCGGTGTGGGAGCTGTTCTGGTGGAGCCTCGCGGGGGCGTCGGTCCATCTGCTGGAGCCTGGCGGCGAAAAGGATCCCTCGCTCCTGCTGCGGGCGATCCGCGAGCAGGGCATTACGACGATGCACTTCGTGCCGTCGATGCTGGGGACGTTCCTTCCGTATGCGGCGGCCTTCGGCGGCAGCCGGCCGCTGGCCGGCCTGCGGCTCGTCTTCGCAAGCGGCGAGGCGCTGAAGCCGGCCCACGCCGCCCAGCTGGCGCAGCTGCGGCCTGCGGGCAGCCCGCTGCCGAGGCTCGTCAATCTGTACGGCCCGACGGAGGCGGCCGTCGACGTCAGCCATTACGACTGCGCCGAGTACGGCGGCGGACCGCTGCCGATCGGCCGCCCGATCGACAACATCGCCCTGCATGTGCTGGACGAGCGGCTGCAGCCGCTGCCGCCGGGCGCGCCGGGAGAGCTGTGCATCGCCGGAGCCGGACTTGCCCGCGGCTATTTGAACCGGCCCGAGCTGACGGCGGAGAAGTTCGCCGCGCTGGCGGACGGCACGCGCGTCTACCGCACGGGCGACGAGGCGCGCTGGCTGGCGGACGGATCGCTGGAATACCGCGGCCGCTTCGACCATCAGGTCAAGCTGCGCGGCCAGCGGATCGAATGCGGCGAGATCGAGCAGGCCGCGATGGACGTTCCCGGCGTCCTGGACGCCGTGGCGATGCTCGCGGACGATCCGCTCGGCGAGCCGCAGCTATGCCTTTACGTCGCCTGCGGGCTGACGGAGCCTGAGCGCGCCGAGCTGGCCGCGAGGACGCTGCCGCAGCGGCTTGCCAGGCGGCTGCCCGATTACATGCTGCCGGCGCGGTTCGTGGCGCTGGAGTCGTTTCCGCTGACGCCGAGCGGCAAGACCGACCGCAAGCGGCTGCCGGCGCCGGACTGGAGCGGGGGAGCGCCGACGGGCAGGCCGCCGGCCGGCGAGGCCGAGCGGAGGCTGGCGGAGCTGTGGACGGAGCTGCTCGGCGTCCGGGATTTGACGGCGGAGACGCATTTCTTCCGCGCCGGCGGCCACTCGCTGCGCGCGGCGCAGCTGGCCGGAGCGATCGAGCGGACGTTCGGCGTCCGGTTCTCCTTGCGGGATGTGTTCGAGGCTCCCGTGCTGGAGGAGATGGCGCTGCGGGTCGGCCGGGCCGAAGCATCCGGATCGCCGCCTCTTCCGTCGGCGGGAGAGCGCGGGCATTATCCACTGACGCCGGCCCAGAACCGGCTGTTCATCCTGCATCGGCTCGATCCGGACGGCATCGCCTACAACCTGCCGCTCGGCCTCCGGCTGGAGGGAGAGCTCGATGAAGAGCGGCTGCAGCGAGCGCTGCGCCGGCTGGTCGAGCGCCACGAGGCGCTGCGCACCCGCTTCGGCTGGAGCGACGGCCATCCGGTCCAGATTGTCGAGCGCGATGTCGTCCTGACGGCAGAGCGGCTTGCCGGGACGCTGGAGGAAGCGTCGGCCGGCTTCGTGCGGCCGTTCGATCTGACGCAGGCGCCGCTGCTGCGCGCCGGCCTGCTGCGGGACGAGCGCGGAGGGGCGCTGCTGCTCGACATGCACCACATCGTCTCCGACGGCCTCAGCCTGAACGCGCTGGCGCGGGACTTCGCGGCGTTTTATGACGGCAGGGAGCCGGAGCCGCTGGCGCTGCGGCTCGTCGACGCCGCCGTCTGGCAGCGGAGCTGGCTGGAGACGCCGGAGCGGGAGCGGCAGGAGCGCTACTGGAAAAGCAAGCTCGCCGGCCCGCTGCCGGCGCTCGACCTGCCGCTGGCGGCTCCGCGTCCGGATCGTCCGGACGGCCGCGGCAGCCGCGTCGCCCGGATGCTGCCGGAGCCGGTCCGCCGCTCGGCGCTGCGGCTCGCGGAGCAGCTGGAGGCGACGCCGTATCAGGTGCTGCTGGCCGCTTATGCCGCGCTGCTTTATCGGATGACCGGGGAGGAGGACCTGATCGTCGGCACGCCGGCAGGCGGGCGCTTCCACCCCGATCTGCAGCCGGTCGTCGGCATGTTCGTGCAGACGCTGCCGCTGCGCCTGCCCGCCGCGGGAGCGTCGAGCTTCCGCGAGCTCGTCGCGGCGGCGGGGCGCGCCAGCGTCGAGGCGATGGACCACGGGCAGCTGCCGTTCGAGCTGCTGGCCGCCTCGCTCGGCGCCGGCCGCGATCCGAGCCGCAACCCGGTGTTCGACACGATGTTCGTCTGGCAGAACATGGAGCCTCCGGTCCGCGAGGCCGGCGGGCTGCGGCTCGAGCCGTTCCGGCTGCGGCAGGACGCCGCCAAGCTCGACCTCACCTTCGAGCTCGCGGAGCGCGAGGAAGGCGTGGAGCTGACGGTCGAGTACGCGTCGGCGCTGCTGACGGAGGAGGACGCCAGCCGCATGGCCGGCTGGTACGTGGCCTTGCTCGAGGCGGCCTGCGCCGATGCCGGCCGACCGCTCGCCGAGCTGCCGCTTCTGACGGCGGCGGAGGAGCGCGAGCAGGAGCGGCGATTCCAACCGGCGGATTCGATCGCGACCGGTCCGGCGGAGCCCGGCTTCGCCGCTGCGGCGGAGCCGGCTACGCTGGACGGCGTGCTGCGCCGGCAGGCGCGGCTGGCGCCGGAGGCGCTCGCCGTGAGCAGCGCGCACGGATCGCTCACCTACCGCCAGCTCGACGAGGCGTCGAACCGGCTCGCCCGCGAGCTGCTGGCCCGCGGCGTCGCAGCGGAGGCGCTCGTCGCCGTCTGCATGGAGCGCCGCCCGGAGCTGATCGTCGCGATCTACGGCATCCTCAAGGCGGGAGCCGCCTATGTGCCGCTGTCGCCGTCGCTGCCGGCGGAGCGTATCGCCTACATGCTCGCGGACTCCGGCGCGCCGCTCGTGCTGACGGCCGGGGACGTCCGGCTGCCGGAAGGGCGGCGGCGACGCGCCTCGACGTCGCGGAGGCGGTCGGCCGCCACGACGATCCGGCGCCGCCGCCGGCCGGCCACGGCGGAGGCAGCCTGGCCTATGTGCTCTACACCTCCGGCTCGACCGGACGGCCGAAGGGCGTCATGGTCGAGCACCGCTCCGTGCTGAACCGGCTGCGCTGGATGCAGCGGGCCTATCCGCTGGCGCCGCAGGACGTCATCCTGCAAAAGACGCCCGTCACCTTCGACGTCTCCGTCTGGGAGCTGATGTGGTGGAGCTTCGCCGGAGCGTCGGCGCATCTGCTGGAGCCGGGCGGCGAGAAGGACCCGTCTGCGATCGCGCGCGCGGTCGCCGAGGCGGGAGTGACGACGATGCACTTCGTGCCGTCGATGCTGCATCTGTTTCTGGAGGATGCGGCGGCGCGGCAGGCGGCGCGAGCCGGCTCGCTGGCGACGCTGCGCACCGTCTTCGCGAGCGGCGAGGCGCTGGGCGCGAGCCTCGCCGAGCGGTTCGAGGCCCGCATCCGCAGCGCCTGCGGGGCGGAGCTGGTCAATCTGTACGGCCCGACGGAGGCGACCGTCGACGTCGCCTTCTACAACTGCAGCCGCGAAGGCTTGCGCGGCGGCGGCGTGCCGATCGGCCGGCCGATCGACCGGACCGCGCTGTACGTCGCGAGCCCGGGGCTGCGGATGCAGCCGCCCGGCGTGCCGGGCGAGCTGTGCATCGCCGGCATCGGCCTCGCCAGGGGCTATCTCGGACGGGACGAGCTGACGCGCGAGAAGTTCGTGCCGAACCCGTTCCGCGGCGGCGGCCGTCTGTACCGCACCGGCGATCTGGCCCGCTGGCTGCCGGACGGGCAGCTCGAATACTTGGGCCGGCTCGACCATCAGGTCAAGCTGCGCGGCTACCGGATCGAATGCGGCGAGATCGAGGCCGCGCTGCAGCGCGATCCCCGCATCGGCGAGGCGGCCGTGCTGCTGCGCCGCCGCGCCGGAGACGAAGGGGCCGATTATCTGTGCGCCTACTACACGGCCGCAGCGGTCCTGCCCAAGCGGGAGCTGCGCGAAGCGCTCGCCCGCGAGCTGCCCGACTATATGATTCCGGCCGCGTTCGTCCGGCTGGAGCGCATGCCGCTCTCGCCGAGCGGCAAGACCGACCGGCGGGCGCTGCCGGAGCCGCAGCCGGCCGATCCGGCCGGCGAAGTCCGCGAGCGGCCCGGGACGGAGACGGAGCGGGCGGTGTCGGCGCTGTGGGGCGAGCTGCTCGGCGGCGGGGAGCCGGACGTCCGGCGCAGCTTCTTCGAAGCCGGCGGCGACTCGCTGCTGCTGCTGCGGCTGCATCAGCGGCTGGAGGAGCGCTATCCCGGCGCGCTGCAGGTCGCCGATCTGTTCAGCTACCCGACGGTCCGCAAGCTGGCCGCGCGCATCGACAGCAGGTCCGGGGACGATGCCGTCCTCGAAGGGCCGGTCGTGGCGCTTCCCGGCGAGCCGCCGCAGACGGTCCGCTCGGGACCGAGGGAGGGCCGGCTCGACATCGAGCTGGAGCCTGCCGCCGCCGCCGCTCTGGCCGCCATGGCGCAGGAGCGCGGCGCGCGGCTCGAAAGCGCGCTGCTCGGGCTGTACCTGCTCCACTGGAGCCGGACGGCTGGCGCCGAGCGCATCGGAGTCGCCGCGACGGTCGGCCAGGGGCGGATTACGGTATGGAACGCCGATTTTCGGGAGCTGGCAAGCATGGAGCAGCTGCTGGACGCGGCCGAAGCGGCGCTGGCCTCCGGCGTCGGCATCCCTGCGGAGCGCATCCGCCGCGTCCGCCCGTCCGCCGGCCGCTGGAGCGCCGCTCCGCTGTTCCGGCTCGAATCGCCGGAGACGCCGCTGCCGCCGGCAGGCGAGCTGCTCGACCGCTTCGATCATCAGCTGAGCGTCTGGGCCGGCGAGCCGGGCTTGCCGCTCCGCTGCTCCTGGACCTACGCCGCCCGGCAGTTCCCGGCCGAGCTCGTCCGAGGCTGGGCCTCCGGCTATGCCGAGCTGCTGCGCGGCGCGGCGGCTCTGTACCGGGAAGCCGCCGCGAGCCGGCCGGACGAGCAAGACCAAGGAAAGGGGATTATCTCCTCATGAAAAAGATCGCCTTCGCGATCGCCCGCATCGCGTTTTATCTCGGCGTGTTCTACGCCCTGCTGTACGGGCTGAACCATCTGTACCGGATCGACTGGACCGCTCCGTTCGTCGAGCTGCTCGGCCGCAATCCGGCCTTGTTCATGGCGACGCTGTTCGCGTCGATTACGCTTGTCTACGCGCTTGCCTTCGCAGGCGTCCGCCGCCTGACGCGCGGCGGGTCGCCCTCGCTGGCCGAAGCGGCTGGACTGCACCGCCTGCCGGCTGGAGCCGCGCTCGGCTGCGCGCTCATCGGCGTGCTCGGCTGCCTGTTCAGCATCGGCCTGATCGAGATTCCCGCCGTCGCGGAAGCCTATCCGTCGATTCCGGCGCTCGTGGACGACCTGCTGCGCGGCGATCATCTGCTGCTCGCCATCCTCGGAGCGGGACTTGTCGCTCCGGCTTACGAGGAGCTGCTGTTCCGCGGGCTCATCCTGCGGGAGCTGCGAGGCATGATGCCGGCCGCGGCGGCGCTGCTGCTGCAGGCGCTCGCATACGCCTATTTCCAGCCGAGCCCGGCGCTCTCGGTCATCGGCTTCGGCTCGGGGCTGCTGTACGGCTACCTGCGTATCTCGCTGAACTCGCTGTGGGCGCCGATCCTCGTGCAGATCACGGCGATGAGCCTGATCTTCGCGGCCAAGCCGGCCGGCGTCTACGAGGCGGTCGGCTCGCTGGGCGGGGCCGGCGCGGCGTCGGTCGCGGCGGGCAGCCTGCTGCTGATGCTCGCCGCCGCCGGATGGCTGCGGCTCCGCTACGCCTCGCGGCAGCGGCTGGCGGACGCCGCCGGCGAGCGCGCGAATTTGAGGGAAAGGACGGTCCAAGGATGAACAAATGGAAAGACGGCCTGCTGCGTCCCGTCGTCATCATCGGCATCTATTTCGCCTGGTTCTTCACGGTTACGACGCTGTTCTTCGACTATGTGTACCGGGATACGGCCTGGTTCCAGAAAAATACGCTCGTCACGATCCTGCTCAACGACATCGTCGGCCTGCCGCTCATGATCGGCGCGATCTGGCTGCTGTTCCGCCAGAATCTGTTCCGCGAGGCCCGCTTCCGGCGGATCGAGCCTACGTCCGTGCTGATCTGCGTCTGGATCGGCCTCGGCGCCGGGCTGTTCACGGCCGCGTTTTCGCAGCTGCCGCTCATCCGCTCGTCGGACTACCAGTTCCAGACGCTGTTCGACTACATCAACCGCGCCGACTGGTACGTCTTTCTCGGATTCCTGCTGCTCGGCAACGTGTATAAGGAAACGCTGTTCCGCGGGCTGCTGCTGAACAGCTTCCGCCGGCTCATGCCGGTGTGGGCGGCGATCGCGCTCCAGGGGGCGCTGTACGGCGCGCTGTTTTTCCTCGGCGACGTGCCGCTGTCGCTCTACGGCTTTCTCGGAGCGGTGCTGTTCGGCCTGCTCTACGTCCGGCTCGACTCGATCTGGGCCCCGATTGCCGCGCAGATCGCCTGCCAGGGGCTGCAGTACGCGCTTTGGCATTACGCGCCGGATCTCGGCGGCGCAGCGGCGCTCTCCGTCATCATGGCCGCTTCGCTGGCGATGATCGCCGCGGGCGTGCTGCTCCTGTTCAAAAGGCAGCCGGCGGAAAAGGCGCCGGCCGGAAGGACGGCGAGCGCATGAGAACGCTGCGCGCGTTCGCCGAGGCGCTGCTCTATGTCGGCCTGTACGCCGCCATCCTGACGCTCGCCAGCAGCTATCTGTACGGCAGCGGCTCGCCGCCCACCCTGCGCGAGTGGCTCGCCGCCAATCCGAACGGCCTGCTGCTGCTCGTCAATCCGCCCGTGCTGCTTGCCTATGCGCTGCTGCTGCGGCTGCAGCGCGTCGAGGCGGCGGAGCTTGGCCTCGGCCAGCCCCCGCGCGGATGGGCGGCCCCGGCTCTGTCGGGCGTCTGGCTCGGGCTGTTCATCGCCTCGTTCACCGGCCTGCCGCTCGTCCGCGAGGAGCTGCCGGCGATCGCCGGACTGGCCGGCTTCGTAGCCGGCGGCAGTCCGCTCGTCTTCCTGCTCGGCAGCCTGCTGCTCGGCTCCTTGCTGGAGGAGCTGCTGTTCCGCGGCCTGCTGCTGCGGGCGTTCCGCCGCAGCTTCGGCCTTGCCGCCTCCGTCGCGCTGCAGGCGCTGCTGTTCGGCGCGGTGTTCCTGAATGTCCAGACCGGCCTGTTCGCGGCGCTCGGCGCGCTCGTCTACGGCCTGCTGCGCGCGGCGGGCGGCTCGCTCTGGATCTCGCTCGGCGCGCATCTGCTCAGCACCGCCTCCGTTTATGCCGCGGCGCTCCTGCTGCGCGGCGCTCCGGCAAGCCTGCTGCTGATCCTCGCGGCGGGCAGCGCGGTGGCGCTTGCGCTGCATCTGGCGCTGACGCTCGGAGGCGGCCGCCGTGCGGCGGCTCCGCGCCTCGAGGCGCGCGGCTGATGCCGCGGCGCGGTTCATCGTCTTCGTTGTCAACTGCCTGGAAAAAGGGGGCCATACGATGTTTGACCTAAGCAAGCTCGGCGGCGCTGCCGTTCCGGCTCCTGCCGCAGGCATGGGGCCGGCTGCCGGCCTCGTGTCCGCGGCGGAGGCGGCCGCCGGCGGCCACGAGATCGCGATCATCGGCTTCGCGGCGCGGATCGGCGCGGCGAGCGAGCCGGAGGAGCTGGCGCGGCTGCTCGGCGCGGCCGACGACCGCATCGGTCCGCTGCCGGAGACGCGCCGGCTGGAGCTGGAGCCTTATTTGCGAGGGCTCGGCCTGGACCCGTTGGAGGCGGAGTTTTTCGAAGGCGCGTTCCTCGACGATATCTCCTCGTTCGATCCGGAGCTGTTCCGCCTGTCGCCGAAGGAAGCGTCGCTGATGAATCCGAACCAGCGGCTGTTCCTGATGGCGGCGCGGCAGGCGATTGAGCAGGCCGGCTATGGAGGGAGCGCGCTCGGCGGCTCGCGGACAGGCGTTTATGTCGGCTACAACGCCGATGCCCAGCATGACTACAAGCGCATGATCGAGGCGCTCTGTCCGGAGGAGCTCGGCTCCTCGGCGCCCGGCAACCTCAGCTCGATGATCGCCGGGCGGGTAGCGTACCTGCTCGACCTGCACGGGCCTGCGCTGCAGGTGGACACCGCCTGCTCCTCGTCGCTCGTCGCCGTGCATCTCGCCTGCCAGGCGATCCGCTCCGGCGACTGCGACGCGGCGGTCGCAGGCAGCGTCAAGATCAATCTGCTTCCGCTCGACAGCGGCGTGAGGCTCGGCATGGAAGCCTCGGACGGACGGGCGCGTCCGTTCGACGACGAGGCGGACGGCACCGGCATGGGCGACGGCGTCGTCGCCCTGCTGCTCAAGCCGCTCTCCGGGGCGCTTCGCGACGGCGACTTCATCCACGGCGTCATCAAAGGCAGCGCGGTCGGCCAGGACGGCAGCTCCGCGGGCATCACCGCTCCGAACGCGCTCGCCCAGGAGGATGTCGTCGTCCGCGCCTGGGAAGACGCCGCGGTCGACCCCGAGTCGATCGCCTATGTCGAAGCGCACGGCACCGGCACCTCGCTCGGCGATCCGATCGAGATCGAAGGCTTGACGAGGGCGTTCCGGCGCTATACCGACAGGCGGCAGTTTTGCGCGGTCGCCTCCGTCAAAAGCCAGCTCGGCCATCTCGACCATGCGGCCGGCATCGCCGGCCTGCTGCGCGGGCTGCTGGCGATGAAGCGGGGCGAGCTGCCGCCGAACGCGCATTTCCGCCGTCCGAACCGCAGCATCGGCTTCATCGGCTCGCCGCTGTACGTCAATGCCGAGCCGGCGCCGTGGCCGCGCCGCGGCGGTCCGCGCCGCATGGGCGTCAGCGCCTTCGGCATGAGCGGCACGAACGCGCATGTCGTGCTGGAGGAAGCCCCTGAGCCTGCGCCCGTCCGGTTTGCGGAGGGAAACGGCAGGCCCGGCCTGCTCGTCCTCTCTGCCCGCTCCGCCGCCGGGCTATCCGGCTATGCGGAGCGGATGCTCGCCTGGCTGGCGACGTACGACGCTCAGGCGGCCGGGCTGGATGCGATCTGCGGCACGGCGGCGCTTGGCCGCAGCCATGAGCGCTATCGGCTGGCGATCGCCTGCGCCTCTGCGGAGCAGCTCGCGCTCGCCTTGGCGGAAGCGCTGGCCGCGGGGCTGGACGGCGCGGCGGCAGGCGTCGAGGGCGACGCGGGGAATGAGGCCGAGCGCGCTGACGGAAGCGGCGCGCGGCTCGGCGCGAATGGCGAAGCCCGCTGGGAAGCCGACGGCATGGCGCTGCGGCTGCGCTCGCCGAGGCTGGAGGCCGCTACGGCCGTGTTTTGCGGCGCGCTGCCTCCAGCTGGACGGAGCTTGAATTCGAGCTCGTCAGGATCGCCGCTTTGGAGCGGAGGCGAGGCGGCTGCGGGGCCAGCGGAGCGGCGCTCGTCCGGCTCCGCTGTCGACGCCGAGGAGGCGGCCGAGCTCGCGCGGCATTACGCCGAAGGGGGGATGCCGCGCTGGGCGCGCCTGCATCCGCCGGGCTCGCTGCGGCGGGCTCCGCTGCCGAGTCCGCCGCTGGAGCTGCGTCGCTGCTGGCTGCAGCCCGCGCCGAGCGCCCGCTCGGAGGAGAGCCGGGATGAGAGACGGAATGATAGATGGAATGAGAGACAGGATGCGCGAGAAATGGAAAGGAGGGAGATGACGGAACAAGCCGCCGCTGCGGTCCGGCTGACGGATGCCGCGGCTGATGGAGAAGCGGAGGCCGGCAGCGCAGGCAGCTCTCGCCTGGAGGCGCTGCAGGCGGCTGCCGACGCCTGGGGCGAGGCGCTCGGCTATGGGGAGCTGAGCGTGCGCTCCAGCTACTACGAGCTCGGAGGCGACTCGATTCTCGCGCTGCGCACGGTCGGACGGCTGTCGAAGCGTCTCGGGATCGAGGTGGCCGTGCACGAGCTGCTGGGGCAGCCGGTGCTCGGCGACTTCGCGGCGATGCTGCAAGCGAGGCTGGACGCGGTCCGCGCGGCGCGGCGGGAAGCCGGCAGCGGCGGACTGGCCGCGGCGGCGCTGGAAGCGCCGGCGAGCGCGGAGCCGGACGGTTCTTCGCGGCAAGAGCCGCCGCAGAGGCCATCGTCGGCGTCGTCAAATCCATCGCAGGCTGCCGGATCGCCGCAGAGGCCATCGTCGGCGTCGTCCGATCCGTCGCAGACAACCGGATCGCCGCAGAGGCCCTCGTCGCCTCTGTCCGATCCGTCGCAGACGCTCGGATCGCCGCCAGAGGGCGAAGCGCCGCTTCCGGGCTTCCCGCTGCCGGCCGAACCTTTGCCGCAGTTGGAGGCCGGCGCTGCGGAAGGCGCCGCGGCGCCGATTCCGCTCGTCGCCGAGCAGCCGCATTACGCGGTGTCCTCGTCGCAGCGCCAGATGTACCTGCAGCAGCAGGCGCAGCCGGAGGACCGCAGCTACAACCTGCCGGAGCTGCTCCAGCTGTCCGGCGAGGTCGACGCGGACCGGCTCGAGGAGGCGATCCGCGCCTTGATCCGCAGGCATGAGCCGCTGCGCTCCTCGTTCGCGATCGTCGACGGCGAGCTCCGCCAGTTCGTCCATGCGGACGCGCCGTTTCGGCTCGGCCGGCTGGAGGCGGAGCCGGAAAGGCTGGACGAGACGCTCCGCGCGCTGTCGCAGCCGTTCCGGCTCTCGCAGGTCCCGCTGCTGCGGGCGGCGCTCGTCGCGACCGGCTCGAATTCGCCGCTGCTGTTCCTCGACCTGCATCATATCGCCTCCGACGGCATGTCGGCGGGCATTCTGCTCGAGGAGCTGCTGACGCTGTACGGCGGAGGCATGCTGCCGCCGCTGCCGCTGCGCTACCGCGATTATGCCGATTGGCAGCAGCGGACCCTCGGCTCGGAGCGGCTGGAGGGGCAGCGCCGGTACTGGCGGGAGCGGATCGCGGACGACTGGCCGCTGCTGGAGCTGCCCGCCGATTTTCCCCGACCGCCGGTCAAGGACGGCAAAGGGGCGACGTTCGAGCTCGACCTCGAGCCCGGCCTGGCGGCGGCGGTCAAGCGGTTCGCGGCGGCGAGCGGCTGCACGCCGTTCGTCGTCCTGCTGGCCGCCTATCAGGCGCTGCTGGCCAAGCATGCGGGCGCCGAGGATATCGTCGTCGGCACGCCCGCCGCTGGCCGGCCGTCGCCGCAGCTGGAGCGGCTGGCCGGCATGTTCGTCGGCACGCTGCCGCTGCGGGCGAAGCCGGCTGCCGCCAAGACGTTCGCGGCGTTCCTCGCCGAAGTGCGGGAGACGGTGCTCGAGGCGTTCGCGCACGGCGACGTGCCGTTCGAGGAGCTGGTCCGCATGGACGGGCGCCGCGATCCGAGCCGCAGCCCGCTGTTCGACACGATGTTCATCATGCAGAACCTGCGCATCCCGGATCGCGGCGAAAAGGGACTTTCCTATACTCATCGACGCTACGAGCATGGCACGGCCAAGTACGACCTGATGGTCCAGGCGGTCGAGCGGCCGGACGGGCTGCGGCTCGTCGTCGAATACGCGGTCTCGCTGTTCCGCGAGCAGACCGCGCGCACGCTGCTCGACCGTTATGTCCGCCTGCTCGGCGCCTTCCTCGCCGATCCGGAGCGGACGCTCGGCGAGGCTGACATGCTGTCCGCCGCGGAGCGGGAACAGCTGGAGCGCTTCGGCCGGGGGCCGGAGCTCGGGCTGCCGCCCGTAAGGGCCGAGCGGCTGGTCGAGGCTTGGGCGGCGGAGCGGCCCGACGGCGTTGCCGTCATCGGCAAGGATGGCGCGCTCACGTATCGCGAGCTGAACGAGCAGGCGGAGCGGGTCGCCGAGCTGCTGCGGCGCGAGGGAGCGGAGCGCGGCTCGATCGTCGCCGTGCTCGCCGAGCGCTCGCCCGCCATGGTCGCGGGGATGGTCGGCGCGCTCAAAGCCGGCGCCGCCTACCTGCCGCTCGATCCCGCCGCGCCGCCGGAGCGGATCGCCTCCATGCTCCAGGACAGCGGCGCCTGTCTCGTGCTGACGGACCTGCCGGAGGAGGCGCCGGCGCGCGCGGCGCTTGCCGGAGCCAGGGAGCTGAGGCTGTCCGCAGCGTCCGCAGCGCTGCTGGAAGCAGATGCAGGCAGCGCCTGGAGCGCAGCCAGCGGGACGGGCGCAGGCAGCAGGAGCGCAGCCAGCAGCTGGAGCGCCGGCGGCGTCGGCAGCCGGGCGGATCAGGCGGGCCCTGCACCGGCGGCGGACCGCTTCTCCCCGTCCGCATCGGCGAGTCCGCAGGCTTTGCCGCAAGCCTTGCCGCAAGCCTTGCCGCAAGCCTTGCCGCAACACTTGCCGCAAGCCTCTGCGGACGGCGGCCTGCTCTCGCCGGAGGACCCGATGTATGTCATCTACACATCCGGCTCGACCGGGCGGCCGAAGGGCGTCGTCGTCCCGCATCGGGCGTTCCACGCCTTCGCCGCCTCGATGAGCCGGCTGCTCGGCGGCGTCGGTCCGGACGACCGCTGCCTCAGCCTGACGAGCCTCGGCTTCGACGTCAGCGTCTGCGAGCTGTTCCTGCCGCTGCATGCGGGGGCGGCGATCGTGCTCTATCCGGACGACCGGCTGCTCGATCCGCCGCGCATGGCCCGGGTCATCGCCGAGGAGGGCGTCACGTTCGCCTATCTGCCTCCGACGCTGCTCGGCGACGTTGCCGGCGAGCTGGAGCGGCTCGCCGCAGCCGGGGCGGAGCTGGCGCTATCCCGGCTGCTCGTCGGCGTCGAGCCGATCCGAAGCGGCGTGCTGGAGCGCTTCGCGGCGCTGCGTCCGGGCATGGCGATCGTCAACGGCTACGGGCCGACCGAGGCGGCCGTCTGCGCGACCGCCCATGTGTTCCGTCCCGGCGGCCCGCCGGAGGCGATCGTGCCGATCGGCGGCCCGATGCACGAGACCGACATCATGCTGCTCGGCTACGGAAACGCGCCGGTGCCGCCGGGCGCGCTCGGCGAGCTGTGCATCGCCGGCAGCCATCTGGCGCTCGGCTACCTCGGCCGGCCGGAGCTGACCGCCGAGCGCTTCGTGCCCGACCCGCGCCGGCCTGACCGGCTGCTGTACCGGACCGGCGACCTGGCGCGCTGGCTTCCAGACGGCCAGGCGATGTACGCCGGCCGCATCGACCGGCAGCTCAAGATCCGCGGGGTGCGGATCGAGCCGGCCGAGATCGAGGCGAGGCTGCTGCAGCTGGACGGCGTGCGCGAGGCGGTCGTCGACGCCCGCGTCCTACCGGACGGAGACAAGCAGCTCTGCGCTTATGTCGTGCTCTCCCGCGAGGGCGGGACGAGCGGGCTGCGCGACGAGCTGAAGCGGCTGCTGCCGGAGGCGATGCTGCCCTCCTTCCTGATCGAGCTGCCGCGCATCCCGCTGACGCGCAGCGGCAAGGTCGACCGCCAGGCGCTCCCGGAGCCGCTCTCGCAGGCGCACGGCGGCGTGCCGGACGCGAGCGGCGCTCCGTCGACCGAGACCGAGCGGCGGATCGCCGCGCTTTGGCGGGAGACGCTCGGAGTCGAGCGGGTCGGCCGCACGGACGGCTTTTTCGAGCTCGGCGGCCATTCGCTCAAGGCAGCCGCGCTGGCCGGCCGCATCCGCCAGTCGTTCGGAACGGAAATGCCGCTGCGGGCAGTATTCGAGCATCCGACCGTCGCGGGCATGGCGGCATGGCTGGAGACGGCGGCAAGCGGAGGCAGCGCCGCGACCTGGGGCATCGAGCCGCAGGCCGCGAGCCTGCCGGGCGCCGGCACGGAGCGGGGCATGGCGGCGGAGGCCGGCCGCGCCGGGGAGCGGGCGCTCGGATCGGCCCATTCGATTCCGCGCGCGGAGGAGCGTCCCTATTATCCGATGTCGCGGACGCAGCGGCGGCACTATGTGCTGGAGTGGCTCGGCGGCGGCAGCGCCGCCTACCATGTGCCGCTCGCGCTGCTCATCCGCGGTCCGCTGGACGCGGCGCGGCTGGAAGGCGCGTTCCACGGCCTGATCGCCCGTCACGAGACGCTGCGCACGGCGTTCGTCCACGAGCGGGAGGAGTTCCGGCAGATCATCCGGCCGGAGGCGGAGTTCAGGCTGGAGCTCGGCCGTCTCGACGAGGAGGAGAGGCGGGGGCTGCGCTCCGGTCCGCAAGGGGCGGCTGCCGCGCAAGCGGTCCGCCGGCGGATGGCGGAGCTGCTCCGTCCGTTCCGGCTCGATGCTCCTCCGCTGCTGCGGGCGCGGCTGCTGGAGGGCGATGCCGACCGCCATGTGCTGCTGCTGGATTTCCACCATCTCGTGACGGACGGGCTGTCCATGCCCATCGTCCTGCGGGAGCTGCTCGCGCTGTACGACGGCCGGGAGCTGCCGCCGCTGCCGATCCGCTACCGGGACTATGCGCTGTGGCAGGAGCGGAGGCTGGCGGAGCCGCCGCCCGGGCGCTGGCTGGAGCGGCTCGCGGGCGAGCTGCCGCCGCTCGAGCTGCCGCTCGACCGTCCGCGTCCGGCTGCGCGCTCCGGACGGGGAAGGCGGCTGGAGTTCGCCTTCGACGAGGCGACGAGCGCCGCGATCGCCGGCTTCGCGCGCGGCGAGGGCGTGACGCTCTACACCGCGCTGCTCGGCGCCTATATGAGGCTGCTCGCCGTCTACGGCGGAGCGGCCGAGGTTCGCGTCGGGTCGCCGGCGGCCGGCCGCTCGCATCCGGACGCCGACGGGCTCGTCGGCCTGTTCGTCCATACGCTCGTCCTGCGCGGCTATCCGGCCGCCGAGCGTCCGCTCGGCGAGTTCCTGCAGTCGCTGCAGCAGGACGCGCTGGAGGCGCTGGAGCATCAGGAGCGTCCGTTCGAGGAGCTGCTCGAAGCGCTCGGAGCGCAGCCGGCGGTCGGACGGCAGCCGCTGTTCGACTGCATGTTCGCGCTGCAGAACATGGAGCTGCCGGCTCTGGAGGGAGGCGGGCTGACCGCCGAGACGCTGCCGCTCGATGCCGGCACGGCCAAGTCCGATCTGCTGCTGGAGGCGGCGGAGCGGGACGGGCGGCTGCATTTTCAGCTGGAATATGATACGGAGCTGTTCGCGGACGCGACCGCGTCATGGATCGCCCGGCATTATGCGCAGCTGTGGAAGGAATGGCTCCGGCCCGGCGCGGCTTCGCGGCCGCTGGAGGAGCTGGGCTTGATCGACGGCGAGGAGCGGTGCGAGCTGCTCGGCGAGGTCCGTCAACGGAAGGGAGAGGCGACGATGAACAAGATAGAGGGCGCGGCAGAACCGGAGCGCGCCGGGACGGAAAGCGGCTGGTGCAGCATGATGCGGCAGTTCGAGGAGCAGGTCCGGCTGCGGCCGGACGCTCCCGCCGTGCACGCCGGGGAGGAGACGTGGACGTACGCGGAGCTGAACGCGCGGGCGAACCGGCTCGCCCATGCGCTGAGGGAGAAGGGCGTCGGGCCGGAAAGGCTCGTCGTCGTCATGGCGTCGCGCTCGCCGCGGCTGCTCGCGGCGCTGCTCGCCGTGCTCAAGGCGGGAGGCGCGTTCCTCGCGGTCGATCCGTCGTATCCGGAGGAGCGGATCCGCTGGATGCTGGAGGACGCCGGAGCGGCGCCGGCGCTCGTCGAAGCCGCCTATGCCGGCCGCGCGGCCGGCGCCGCCGAGGAATGGCGGCTCGAGGAGCTGGAGGAGGCGTCCGCGCTTCTGCCGGCGAGCGATCCGGAGCCGGTCAGCCGGCCGGAGCATCTCGCCTATGTGCTGTACACGTCCGGCTCGACCGGCCGTCCGAAGGGCGCGATGATCGAGCATCGCGGACTGGCGAGCTTCCTGCGGCAGTTCGCCGCGCGGCTCCCGTTCGCCGCCGGGCAGGGCGTGCTGGCGATGGCCGCCGTGTCGTTCGATATTTTCCTCGTGGAGACGCTGCTGCCGCTGACGCTCGGCATGCGCGTCGCGCTCGCCCGGGAGGAGGAGCGCGGCGACGCCGAATCGCTGAGCCGGCTCGTCGAAAGGCATGAGGTCGACGTGCTGCAGCTGACGCCGAGCCGCTTCAAGTGGTGGGCGGCGCAGCAAGGCGCGACCGCCGCGTTCCGGCGGCTGTCCGTGCTGCTGATCGGAGCCGAGCCGCTCGCGCCGTCGCTGCTGCAGCGGGTCAAGGCGGCGACGGACGCGCGCATCTTCAACCTGTACGGGCCGACCGAGACGACGGTATGGACGTCCGTGCAGGAGGTGACGGAGCTGGCCGCGGACGAGGCGATTACGATCGGAACGCCGATCGAAGGCGCCCACATGGTCGTGCTCAGCGCCAAGCTCAAGCTCGCGCCGACGGGCGTCATCGGCGAGATCTGCATCGGCGGCGAAGGCGTCGGGCGCGGCTATCTCGGCCATCCGGAGTGGAGCGAGGGCGCATTTGCCGAGCATCCCTATCGGCCGGGCGAGCGCCTGTACCGGACCGGCGACCTCGGGCGGCGGCTCGCGAGCGGCCAGTTCGTCTACGCCGGCCGCCGCGACCATCAGGTGAAGATCCGCGGCCATCGGGTCGAGCTCGGCGAGGTGGAGCGGCTGGCGCAGGAGGCTCCCGGCATCCGCGAGGCGGTCGTGACGGCCGTCGACGAGGAGGACGGAGAGCAGGCGCTGTGCCTGTATGCGGTGGCGGAGCCCGGCCTGGAGGACGGCGCGGACGAGCGGACGAGGACGTATTTGGCGGCGCGGCTGCCGGGCTACATGATTCCCGCGTATCTCATGCTGCTGGAGCGGATTCCGCTGACGCCGACCGGCAAGATCGACCGCAAGTCGCTGCCGAAGCCGCAGGCGCGCGGCGCGGCGGCGTTCGAGCCGCCGGCGGGAGAGCTGGAGCGGCGGCTGGCCGGGCTGTGGCGGGACGTGCTCGGCCAGGAGCGCATCGGCCGCCGGGACGGATTTTTCGAGCTTGGCGGCCACTCGCTCAAAGCGGCGACGCTGGCGAGCCGCATCGCCCGCGAGTTCGGGGCCGACGTCCCGCTGCGGGAGCTGTTCCAGCATTCCACGCTGAGCGCGATGGCGGAGCGGATCGGAATGTCCGCCGCGGCGTTCGAGCCGATCCCGCGCCAGCCGGAGCGCGAGGAGGGATATCCGATGTCCCCCGCGCAGCGCCGCTTGTACCTGATGCAGTGGATGGCCGGCGAGGCGGCGATGTACCATGTGCCGTTCGCGGTCGACATCCGCGGCGCTCTGGACGCGGAGCGGCTCGAGCGGGCGTTCGGGGAGCTGGCCCGGCGTCAGGAGAGCCTGCGCACGACGTTCCATTACGAGGACGGCGAGTTCCGGCAGAAGATCCATCCGCCGTCGGGCTTCGCGCTCGAGCAGGCTCCCGAGCTCGGCAGGCTCGCGGCGGAGGAGCTGGCGTCCGGCGGCGGGGTGCCGGTGCAGAGGCTGATGAAGGCGTTCATCCGCCCGTTCTCGCTCGATCGCGAGCCGCCGGCGCGAGCCGCGCTGCTGCAGCTCGGTCCGGAGCGCCATCTGCTGCTGCTCGACCTGCATCATATCGCGACCGACGGCGTATCGACGTCGCTGCTCGTTCGCGAGCTTGGCGCCCTCTATGCCGGCGAGGAGCTGCCGGAGCCGCCGATCGGCTGCCGCGACTTCGCCGTCTGGCAGCTGGAGCGGCTCGAGTCGGAAGCGATGCGCGAAAAGGAGGCGTACTGGCTTGCCCTCTACGAGGAGCTGCCGCCGGCGCTCGAGCTGCCGCTCGACCGGCCGCGTCCGGCCGCGCCGAGCTTCCGCGGGGCGACGCTTGAGCGGCGCCTCGGCCGGGAGCTGACGGCGGCCGCCGAGCGGCTGGCGGCGGCGCGAGGGGCGACGCTGTTCGCCGTGCTGCTCGGCGCCTACGGCATCCTGCTGGCGAAGTACGCCGGGGAAGAGGACATCGTCGTCGGCACGCCGGTCGCCGGGCGCGGCCATCCCGACGTCGAGCCGCTGATCGGCATGTTCGTCAACACGGTCGCGCTGCGGCTGCGGCCGGCGGGCGAGCTGGCGAGCGGCGACTACATGCGCGGCGTGCAGCGCGATCTCGTCGACGCGCTCGACCGTCAGGACTATCCGTTCGAGCGGCTCGTCGAGCGGCTGGGGCTGCAGGCGGAGGCCGGCCGCAACCCGCTGTTCGATACGATGTTCATCCTGCAGAACATGGAGCATCCGGAGTTCCGCGCCGGCGGACTCGCGCTGGAGCCGCTGCCGTTCGATCCGGGAGTCAGCAAGTTCGATCTGACGCTCGAGGCGGCGGCGAGAGACGGCGAGCTGTCGGTCACGTTCGAATATGCGGCCGACCTGTTCGAGCCGGACACGATCGAGCGGCTGGCCCGGCATTACGAGGAGATCTTGCGCCAGCTGTGCGCGGATGCCGATGGCGCGCGCGCCATCGAAGATTTCGAAGTCGAGACGGAGGAGGCATGGGGATGAAGCTGACGCTGGAGCGCAAGCCTTTCGGCGACTTCTGGATGAACTGCATGCTGAACCAGGCGTTCAGCATCGCGCAGTCGGTCCATCCGAGCTACCGCGATGCGGCGTATCTCAATCTGTACCGCTATTTCCGCTGGGAGGCGGCGACCGACCGCGAGTTCCGCTATCCGACGATCGACTCGCTCTATTATTTGAGCGACACGGAGTGGGAGAAGTTTCCGCTGACCGGCGTCATCCGCCGGATCGTGCCGATGCATTTCCGCGACGAGAGCCGCATGCTGGACGAGATCCGCGACGTGCTGCGGAGCGGGCGCAATCTGAGCCTGAACGTCGATCTGTTCGGCTGGCTGCCGGACAGCATGGCGTGGCAGAAGTTCCATTGGTACCATTACTCGCTGTTCAACGGCTTCGACGAGGAGAAGGGCGTCTTTTACGTCATCGACGACACGCTGGCGGGCTACGGGGAGCATGAGGTGCCGGAGGAGCGGGTGCGGGAGGCGTTCGCGCAGTCGGAATACAAGCTCGATCCGGGCTATGCCGGCCCGGCCTGCTACGTCTATGAGCTGCAGCCGGACATCGTCCCGTTCGAGCTGAGGCTGGAGGAGGTCGCGGCGCACGCAGACCGGCTGTCGCAGGAGCTGGAGGCCTTCGGCATGGACGGCATGTGGCGGGTCGACGAGGCGCCGGGGGAGAAGCGGGAGCAGCAGCTGACGTACGGCCTCGTCGGCATCAACATCATCGTCAACCGCCAGGAGGCGAACGCGGGACTGCTCGAGCGGCTGCGCCTGAAAAAGCTGCTGGAGGACGAGCTGCTGGATGAGCTGGACGAGCAGCTCGGCCGCATCCGCGAGGGCTGGGCGGCGCTCAAGCAGCGCTTCGCCGACGGCAGCTTCCGGCGCGAGCGCGACGCCGAGCTGGCCGAGCGCCTGCTGGCGCGGGAGCGCGAGCTGTGGAGCCGGCTCGCGGCCGAGGCATGAGGCCGCTGCGGCTGTTCTGCCTGCCGCATGCCGGCGGCTCGGCTCAGCTGTACCGGCGCTGGGCGGCCGGCGCTCCGCCGGGACTGGAGCTGGCGCCGCTGGAGCTGGCCGGACGGGGAGTCCGGCTCGGCGAGCCGTTTTATCTCGGCATCCGCGAGGCGGCGGAGGATCTGCTCGGCGAGGTGCTGGAGCGGCGGGAGGAGGGCCGCTTCGCGCTGTTCGGCCACAGCATGGGCGCGCTGATCGCCTATGAGCTGGCCGTGCTGCTGCAGCGCGCGGGCGGGCCGCAGCCTGAGGCGGCGTTTCTGTCGGCCAAGGACGCTCCGCAGGTGGAGCGCCGGGAAGCGCCGATTCACGGCTTGCCCGAAGAACAGTTCATCGAGCGGATCCGCCGTCTCGGCGGCTGCCCGGACGAGCTGTTCGAGCAGCCGGAGCTGCTGCGGCTGTTCCTGCCCGTGCTGCGCGCGGATTTTCGGCTCGTGGAGACGTACCGCCATCAGGACGCGCCGCTGCTGGAGACGCCGGGCGTCGTGATGGGCGGCCGCGCGGACGGGACGCTGTCGGGGTCTTGGGTCGAGTGGCAGCGCTGGTTCGCCGCTCCTTGCCGACTGGAGCTGTTCGAGGGCGGACATTTCTACGCGCAGGAGCGCCATCCCGAGCTGCTGCGGCGGATCGCGGACATCCTCGGGCTCGCACCGGAGAGGGGAGGAGCCGCGCTCGCGCCGCTGGCATCCGGCGCGGGCGGAGGCAGGCTCGGCCTTGGGGGCATAGGGGAAGGGAGGAATTCGCGATGAGAAAAAGACCGGCGCCTGCGCTGCTGTTTCCCGGCCAGGGCTCCCAGCGTCCCGGCATGGGACGGGCGCTGCTGGAGCGGCATGCCGAAGCCCGCGCGGCCGTCGAGGAGGCCGGCGACGCGATCGGAGCCGACCTCGCCCGCCTGCTGCGGGACGGCTCGATGGAGGAGCTGACGCGCACCGAGATCGCGCAGCCGGCGATCCTCGCCGTATCGGTCGCGATGTACCGCGTCTACCGCGGCAGCCTCGGCGGGCCGCCGCCTGGCTGGCTGGCGGGGCACAGCCTCGGCGAGTTCAGCGCCTTGGCTTGCGCCGGCGCGCTGCCGCTCGGCGACGCGGCCCGGCTCGTGCAGGCGCGCGGCCGGCTCATGGCCGAGGCGGCGCGGCGGCAGCCGGGCGGCATGGCCGCCGCGCTCGGCATCGCGCCGGAGCGGGCCGAGGCGATCTGCCGCGAGATCGCGGCGGACGGACGGTTCGGCGTCGTCGTCCCGGCGAACTACAACGCTGCCGCGCAGACGGTGCTGTCCGGCCATTTCCCGGCGCTGGAGGAGGCGGCGCGCCTCGTCCGCGAGGCGGGAGGCAGCACGGTCCGTCTCGCCGTCGGAGGCGCGTTCCACAGCCCGCTCATGGCTTCGGCCGCCGCGGCGTTCGGCGAGGAGCTGAGCGCGGCTCGGCTCGGCTCGCCGCTGCTGCCCGTGCTCTCCGGCGTCACGGGCCGGCGCATGCCCGGCTCGGCGGCCGCGCTGGCGGAGCTGCTGCAGCGCCAGCTGACCGCTCCGGTGCGTTGGACGGCGGTCATGGCGAAGCTGGCGGAGCTCGGAGCTCGAGCGGCGGTCGAGGCCGGACCGGGCGCCGTGCTGCAGCGGCTCGCCGCAGGCTCCGGCATCCGCGTGCTGGCGATGGACGAGGAGGCGGCGCTTGGAGAGCTGGAGGAGACGCTGCGGCGCGGCCGCTGCCTCTCCTATCTCGAAGGCTGCCTCGCCGTCGCCGTCGGCACGCGCAGCGAGGAGGACGACTTGCTCGTCTACCGGCGGGAGGTGGAGGCTCCGTACCGCGAGCTGGAGCAGCTGCTGCAGGCGGCCGAGGCGGAGCCGTCCGCGCCTGTCGACGCAGCCCGGCTGGAGCAGGCCGAAAGTCTGCTCGGCCGCCTGCTCGCGGGCAAAGGGCTGCCCGAGGCCGAGCGGCGGGAGCGGCTGTCCCGGCTCGCCGCCGCGCATGGCCGCCGGCCGGTCGAGGCCGAGGCGCGATGAAGGGCGTGCGGGCGGAGCTGCTCGTGCTGCGCCTGCCGGACAGCCCCGGCAGCCTCGCCTGCGAGCGGCTGGAGGCGGCCGTGTCGCCGGAGCGGCGGGAGCGCTGCTCGCGCTATCGGCGGCGGGAGGACGCGCTGCGCTCGCTGGCCGGCGAAGCGCTGCTGCGGGCCGCGCTGTCGCGGCGGACCGGCAGGCCCGGCGCCGAGCTGCGGCTGGCGGAGAACCGATTCGGCAAGCCCTGCTGGGCGGATGGCCGCTCGGACGGCGGCGGACTGCGGTTCAATGTGTCGGCATGCCGGCCGCTGGGTCGCGGTGCTGCTCGGCGGAGGAGAGGTCGGGGTCGACGTCGAGGAGATCAAGCCGCTGCAGCCCCTGTTCCCGGTCGACTGCCTGCATCCGGCCGAGGCCCGGTGGTGGCGTCGCCTGCCCGAGCCGGAGCGGCTGGCGGCATTTTACGAGCTGTGGACGCTCAAGGAAAGCTATGTGAAGGCGAAAGGAATGGGGCTGTCGCTGCCGCTGCATTCGTTCGCGGTGCAGCCGCTGGAGGGAGGCGGAGCGGCTCTCGCTCCGCCGGACGGGGACTGCCGCCTGCGGCTCTATCCGCTGGCGGAGGACATGCGCCTCGCCGGCTGCGCCATCGACGGCAGCCTGCCGTCGAGTCCGGAATTCTGGACGTTCGAGCAGCTGCTCGAGCGCGCTGCGCCGAGGCGCTGACCCGCTCCGGGCGGCGACGCCGGTCCGGCTGTCCCGGCCGAATCGGCCGTCTCCGCGACCGAGCTCGACAAAGGCCGTCCCCCGCCGCTTGCGCGCGGCGGGGGACGGCCTTGCTCGTTTCGGGCTCGGCTAGACGACCTTCAGCACCGAGATCATCTTCTCATGGCCGGGACCGCAAGGAATGCTGCACTCGATCTGATACTCGCCCGCCTCGCTGAAGGAATACACCTTCTCGTCGCCGGCGTTCATCTTGACCGAGGTGTTGGCGACGCGGATGCCGTGGATGCCGTCGCTTTCCAGCTTGATGCGCAGCGGCTCTCCTTTCTTGATCGTGTAGCTCTCTTGGTCGAACTTGTAGTTGGTCGCTTTGATGACGAGATCCTGCGTCGGCTCGGCCGTCGTCTCGACGGCTGCGGAAGGCCCGTTCGAGGCCGGAGCGGAGCTGCTGCCGCATGCGGCGGAGATCAGCAGGAAGCCGGCTGCGGCGGCGATCAGCGGAAGGCGGCGGAAAAAGGAACGGTTCATAGTCAGTCTCCTTTCAAATGGGGGCGAAGCCGGTCGGACATGCTGTCCCTATCATACCCAATCCCGGCTGCGATCGGAATGAGGCGGGCGGCGGAAGGGTTGAACAAATGATGACAATCTATGTAAGCCGCCAGGCTTCGAAGGGAAGCTTGACGGCGCCGGTCTCAGTGCTGTTCCTTGCGCTTGGCCGCATCGAACGGAGTCGGGATGAAGAGGTCGATGATCCCGATGACGAGCGCGGCGAGAATGGCGCCGAGCCAGGTGACGGCGACTCCGCCGACGATGAACTGGGCGATGTAGAGGACGATCACGCTGGCGACGAAGCCGACGATGCCGCGGCCGAACGGGCTCACCCGCTTGCCGAAGATGCCTTCGACCACCCAGCCGAGCAGCGCGATGACAAGCGCCAGCATCAGCGCGCTCCAGAAGCCGCCGACCGTGAACTGGGGCACGATGAAGCCGACGAGCATCAGCACGATCGCCGATACGATGAAGCGGACGACATGTCCGAGAAAGTTCATGCAAGTTCCCTCCAATCGAGTTGTTCCCGTCTTCCGCGCGGCGCGAGGCCGTCGGTTTCGCCGGGTGCACGGCATTAGCATGGCCGGAATCGGGCCATTTCATGTAGGAAGAGTTCTCGACCCGTGCGCCTGCCGTGCCCATCCGTTATAATGGCCCTAGAGAGGAGCTGTGGACCGTTCGTGGACAGCAAAATTTTAAGCACGCTTGAATATTCCAAGATCATTCATCAATTGATTCAACATACAGCGACTCCGATGGGCCTGCGGATGGCCGAGGAGCTCGCCCCTTCGTCCGCGCTCGAGGACGTCGTCCGCTCGCTGCAGGCGACGGCCGAGGCGGCGAACGCCTACCGGCTCAAAGGGAATCCGCCCTTCCGCGGCGTGGCGGACATCCGCGCCCATCTGAAGCGGGCTGCGATCGGCGGCACGCTGAGCCCCGGCGAGCTGCTCGAGGTCGCGCTGACGGCGCGCGGAGCGCGGCGGGTGCGCAGCCATGTGCTGCACCTGCATGAAGAGCATCCGATGCCGCTGCTGGCGCTGCTGGCGGAGGGCATGTATCCTCGGCGCGAGCTGGAGGACGAGATTCTGGCCTGCATCGACGAGAGCGCGGAGGTGCTCGACGGCGCCAGCGTGGAGCTGGGCCGCATCCGCCGCGAGCTGCGTCAAGGCGAAGGCCGCGTGCGGGAGAAGCTGGAGCAGATGCTCCGCTCCTCGTCCGTGCAGAAGATGCTCCAGGATACGCTCGTCACGCTGCGCGGCGACCGGTACGTCATCCCGGTCAAGCAGGAGTACCGCAGCCATTTCGGCGGCATCGTGCACGACCAGTCGAATTCCGGGGCGACGCTGTTCATCGAGCCGGAGGCGGTCGTGGCGCTCAACAACAAGCTGCGCGAGGTCAAGGCGGCCGAGGCGCGCGAGATCGAGCGCATCCTCCAGAAGCTGACGGCGCTGGCGGCCGAGGCGGCCGAGGATCTGGCGATCAACCATGACGGCCTCGCCCAGCTCGATTTCGCCTTCGCCAAGGCGCAGCTCGCGCATGCGATGAAGGCCGAGCTGCCGCTCATGAACGACGAGGGCCGGATCGTGCTGAAGCGCGGCTTCCACCCGCTGCTCGACCGGACCAAGGCCGTGCCGCTGCATCTCGAGCTCGGCTCGTCGCATAGCGGCATCATCGTCACCGGCCCGAACACCGGCGGCAAGACGGTCGCGCTCAAGACGGTCGGCCTGCTCAGCCTGATGGCGATGTCCGGCCTGTTCGTGCCCGCCGACGACGGCACGGAGCTGTGCGTGTTCGACGCGATCTATGCGGACATCGGCGACGAGCAGAGCATCGAGCAGAGCCTCAGCACGTTCTCCAGCCATATGACCAACATCATCCGCATCCTGCGCGACATGACGCCGAGCAGCCTCGTGCTGCTCGACGAGCTCGGCGCGGGCACCGATCCGGCGGAGGGCTCGGCGCTGGCGATCGCGATCCTCGACCATATCCATCGCACGGGCTGCCGGCTGCTGGCGACGACCCACTACAGCGAGCTCAAGGCCTATGCCTACAACCGTCCCGGGCTGATCAACGCCAGCATGGAGTTCGACGTGGCGACGCTCAGTCCGACGTACCGGCTGCTCGTCGGCGTGCCGGGACGAAGCAACGCGTTCGCGATCGCCGAGCGGCTCGGACTGAGCAAGGCGATCATCCAGCAGGCGCGCGGCGAAGTCAGCGAGGAGGACCTGCGCGTCGAGAACATGATCGAGTCGCTCGAGCGCGACCGCCAACGCGCGGAGCAGGAGCGGGACAGCGCCGAGCAGCTGCGCCGCGAGCTGGAGGAGGAGCGCAGCCTGTACGAGGAGGAGCTGCGCCGCTTCGAGGAGCAGCGCGAGCGGCTGCTCGCCAAGGCTCAGGAAGAAGCGCGGCAGGCGGTGCAAAAAGCCCGCCGCGAGGCCGACGAGATCATCCAGGAGCTGAGGCAGCTGCAGCGCGAGGAAGGCGCGGCGGTCAAGGACCATAAGCTGACCGAGGCGCGCAAGCGGCTGGAGGAGGCTTCGCCGCAGCTGGTCAAAGGACGCCAGGGCGCGCGGCCGGCGGCGGCCGAGCGGGCGATCGAGCCCGGCGACGAGGTCAAGGTGCACAGCCTCGGCCAGCGCGGCCACGTCGTCGAGCTGTCCGGCTCGGAGGCGACCGTGCAGCTCGGCATCCTCAAGATGAAGGTCAAGCTGGCCGACCTCGAGCTGCTGAAGCCGGCGCCGGCGCCGAAGGCCGCTCCCAAAGCGGCTTCATCCACGTTGAAACGCACGCGCGACGACAACGTAAAGATGGAATTGGATCTTCGCGGCTCGAACCTGGACGAATCGATCATCGAGGTGGACCGTTTCCTGGACGAATCCTTCCTGGCCGGCATGGGGCAAGTGTACATCATCCACGGCAAGGGGACCGGCGTGCTGCGCGCCGGCATCCAGGATTTCCTCCGCCGCCACTCCCATGTGAAGAGCTATCGGCTTGGCAACTACGGCGAGGGGGGAGCGGGCGTCACGGTCGCGGAGCTCAAGTAATTCCGAGAGGAAGGGATTGGCGTGAGCGGAATCATCGACGGGCTGTTGGGCAATGCCTATGCCTCTTCCCTGATTTATGTCGCCGTGACGATCATGGCGCTCATCTTGTTCCTGACCTTGTTCGAATGGGTCGCCAAGTACAAGTGCTGGGACGAGATCCGCAAAGGCAACGTGGCGGTGGCGATGGCTACCGGCGGCAAGATTTTCGGCATCTGCAACATTTTCCGGTTCTCGGCCGATGCGGGCGATTCCATCTACGGGAGCTTGATCTGGGGGACGTTCGGCTTCGTCGTACTGCTGCTCGCTTACTTCCTGTTCGAGTTCATGACGCCCGTTTTCCGCATCGACGACGAGATTCAGCGCGACAACCGCGCGGTCGGCCTGATCGCGCTGATCATCTCGGTGTCGATCTCGTATGTCATCGGAGCGACGATCTGACGGCTTGGGGGAGGTAGACATGAAGTACCTTTGGGGCACTTTGGCCGTGCTGGCCGTCCTGTTCTTTGTGCTCGGCATTTTATATCTGGTATGATCGGGTTCGGACAGCAGGATTGGGAAAGGAGCTGCAGCGATGGAGCATCAGCAGCAGGAGGGCGCGGCGGACATCTGTCCGTGGTGCGACTCCGAATTGGTTTGGGACGAGGAGATCGGTCCCGAGGAAGTCTGCCCGCATTGCAGCAATGAGCTGGGCGGGTACCGGACGCTCAGCGTAGGCGGAGCGCAGGCGGAAGAGGAGGACGAGGACGAGGGCGCCGGCTTGGCGGCCGGCCATGCCGGCGCTGCCGCTAGGACGGCCGGAGCGGCCTCGCGCAGCGTCGAAGGCTTGGACGAGGAGGCCGACTGGGAGGCGGGCGACGATACCGGCTGGGCCGGAGCGGGACGTCCGCAGTCGTGGCTGCGCGCCGACGAAAAGGTGCAGCGCATCCTCGACGATCAGGAGGAGATGCCGGAATGCCCGTCCTGCCGCGAGTATATGCTGCATGCGGGCACGAACGCGCTCGGAGCAGGCTCGTTCTCGCCGGTCGAGCCGCCTTCGCTCAAAAAGCCGCTGCTTCCGGATTCGATCCGGCTGCAGCTGTATGTCTGTCCGAATTGCCATGAGGTATCCACGAAGCTGGACCTCGGCTCGCGGACGTTCCTGGCGGAAAGGCTCGACCAGGAAGATTGATCCGGCGATACGCGAACAGCTCTCCGTCCTGCGGAGGGCTGTTTGCGTTCGGCGCCAGCAGGCCGACGCGACGGCCGCTCGCGAATCATCTCCTCCGCGGCAGGGAACCATTTCCGCATGGAGGTGATGTCCGTGAAAAGCGAAAGCGCGCTCCGTCCCTCGCGCGAGGGGGCGCTGCACGGCCAGCCGCTGCTGCTGCTCGCCGTGCTGACCCTGTACAACGGCGCAAACGCGCTGTCCGGCGTTTTCGTGCCCGTTTATCTGTTCAAGGCCAACCAGTCCTACGCGCTTGTCGGCTGGTTCTCGCTGCTCCAATACGCCGCCGGCGGGCTCTGCGTCTATCTGGCCGGCTCGTGGGTGAAGCGCAAGGGCCTCGTCGCCTCCCTGCGCACGGGAATCGCCCTCTCCGGCGGCTTCTACATGGCCGTGCTGCTGCTCAGCGGCAAAGCGGCGGCCTGGGCCGCTCCGCTCGGCCTGCTGAACGGGACGGCGGGAGGCTTCTACTGGCTCGCCTACAACGTGCTTTATTTCGAGATTACGGAAAAGGACAATCGCGACGCCTACAACGGCATGGCGGGCCTGCTCGGCTCCGCGGTCGGCATGGCGGCGCCGTTCCTGTCGGGGCTCGTCATCGCAGGCAGCGGCGGCAACAAGGGCTACACGGTCATCTTCAGCGTGTCGCTCGCGCTGTTCGGCGCGGCCGCCCTGCTCAGCGCCAAAATCCGGAAGCGGCCTCCGCAAGGGCGCTACCGCTGGAGCTTTCCGGCCGCCGAGCTGCGTCAGCGGGCGAGTCCTTGGCGGCGCTTCGCGCCGGCGATCGTGCTGCAGGGGCTGCGCGACGGCGTATTCCTGTTCGTGCTTGGACTCGCCATCTACGCCTCGACGGGAGCGGAGCAGAAGGTCGGCACTTATTATCTCGTCACCTCGCTTGTCGGCATGGCCGCCTTTTGGCTGTGCGGCCGCAAGCTCGGACCGGAGCGGCGCCGCGCGGGGATGCTCGTCGGCACGCTGGCGCTCGCCGCGGTGCTGCTGCCTCTGCTCGGCGGCATGACTTACTCGAGCCTGCTGCTTGTCGGCATCGGCACGGCGCTGTTCTCGCCGCTTTATCTCATCCCGATCACCTCGTCGGTGTTCGATCTGATGGGCCGCTGCGAGGAAGCGGCGGCCAGCCGCGTCGAGCTGACCGTGCTGCGCGAGCTTGCGCTGACCGCAGGCCGGCTCGTCGGCGTGCTGGCCTTCATCTACATCGCCGGCCGCTCGGCCCCGGACTCGCTGGCGTTCGCCTGGCTGCTGCTGGCGCTCGGAGCCGCCCCGATCGCCGGCTGGGCCTTCATCCGCGACCGGCTCCGTCCGGAGGATTCAGCCGTCCGTACCGCGGATCCGGACGGGCATGCCCGCAGGCGCGGATGAACCGCGCGTCCAGCGCCGAAGCTCCTTCGCCGCGCTCGCTCGGCGCTGCCGGACGTACTGGAGGATGACCTCGGGCTCTCCGCCGAACAGCCCGCGATTGGCGGCGCGGCTGGCATCATGCCGGACGGCCGCGGCGATGCCGCCGTGCAGTTCCTCCACGAGACGTCCGATCCGCTCCTCGGTGAAGTCTTCCTCAAGGATGCGTTCGAGCCCTTCGGCGTACGCCCGCTTCCACTCGTCGAACTGCAGCAGCCGGCGCGTCAGCCCGTTGTAGCCCTGCACCCGCACCATGCCGGCGGGGCATAGCTTGCCGTAGCAGTTCCGTCCCCAGGTGCCCTCGTAATCCCAAGGCAGGATGCCGTACTGCTGCCGGGTCGCTTCCTCGTACAACGCGTAGTTCTGCTCGAAGCCGTCGAAGTTGCCGGTCAGCACCGCGCCGGACAGCCAGCGGAAATAAGCGGGCACGTCGAGGCGCTCCTCCAGCAGCTCCCGCAGCTTGGCGTTTTTCAGCCGGTGGATGCCGCGGATGAAGGAGCAGAGGCGGGGCAGCGTCTCGCCGTCGCCCTCGATGAATTCGTAGCCCTCCGCCAGGTCGCGCTTGCGGCGTCCGCTCTCGGAGAGCGAGCGCTCGAAGTTCGCGGAGTCGTTGGCGGCGTACAGAAGCGACCGGTACGGGATGCCGCGGAGCGCGAAGAAGCGGGAATTGACCGCCTCGATCTCCAGATACAGGCCGCGGCATTCGCCGTTCACGTCCAGCCATACATGGCGGGTGCGCGGCGCCGGCACGCCGATGCCTTCCATGAAGCGGAACGAGAGGGCGTTGCGGATCATCGACGGATCGTCCGCTTCCGCGTTCCAGTGCAGCACCAGCCCGCTGTCGAGGCGAATCTCGTACGATTTCTTCGGATATTCTCTCGTATGCCCTCCCCGATAGCGAAGCCTGGCGCCGTCCGTCCTCCCGCCCGTGGTCAGCTGGACCGGCACATGCTTCCGGCTCCATACGTCGCTGGCGAGATCCGCTTGCGCCTGGGCGCTGATCCGAATGGATCGGACCGCCAATCCGGCTCTCATCGCGCACCGCCTCCTTTTTGTCCGCTCCGTCTCCGCTCTTGCCCATGGGATACCGTATTCCGATCCGGCCGGGTTGGTTCGGGGCGGCTTTCGGGCGGGACAGCCCGGCGAGTCCCCATGCGGGTGGCAGACAGGCCGCATAGGATAGAGCAGAGCGGAAGGCGGCGGCGAAGGCAGAGGCAACGCCCCGCTGCGGGAGGGGATCGAGCTGGAAGGGAACGGGTTGACGACGGTGCAGCTGGAGGATGGTGCGATCGAAGCGCTCGTGCGGGCGAGGCGCAGGGATCTGCTTGTCGCGGACGACCCGCTGCGCGGCAGGCGGATCTACATCCCCCTGCATCAAGTGAAGGGGTTCAAGGGAGCGTTTGCGGCGGAGTCGGCCGTCCCGGCCGGAGGCAGCAGGGCGAGCGGCGAGGTTCCGTCGGCGCAGGCGAACGGAGGGAAGCCAGACGACGACGGGGACGGAGCGGAGGCGCTGCCGACGGGCTATCGGGCGATGCTGCTGGAGGCGAAGGGGACATTCGCCGAGGTGAGGCTGTCCGCCCGGCAGGCGCTGCACGGCTATCTCGCCGGCGTGATGAACGATTTCGCGCTGTTCTGCACGCCGCTGCACGGGGCGGTGCTGCTGCCGCTGCAGCATGTGCAGGCGCTCTCGCCGTATCCGGCGGGGCTGGCCCCGTACCGGCTGGAGCCGGAGCAGTTTCCGATCCGCCCGCTCTCGCTCGGCCTCTCCCGTCATTTCGAGCAGCAGCTGGAGCGGCTGGAGGGCGAGATGACGGTGCTCTGCCGGGGCTTCCTGCCGGATGTGGCGGGCGTGCTCGGCCCGGTCCGGGACGGCTTCGTTCCGGTCACGGAAGCGGACGGAGGCAGGCTGCTGCTGCCGGTCTCGGCGCTGCGGGCTGTGTTCCTGTAAGGGCGCGGAGGGGCTTGCAGTCCGCTCCGCATACATAACTCGCGCGGCGGAGGGCATTCTATGGCAGGGCAACTCATCCTGTTCACCGATGGAGGTATCCGATGCAGCCGATTACCGGAAAGGAAATGGAATACATCGCCGATTCCATGTCCAATGAAGACCTGCTCGCCAAGCAATGCGCCTGCGCCGCGACGAGCATCAGCGTGCCGGGCGTCAGCCAGGTGCTGAGCGGCATGGCGTCCGCGCATCAGCAAAACTACGCGATGCTGCTGAGCACGCTCCAGCAGCATCAGCAGCTGGCGCCGACGAGTCCGCAGACGAACTGAGCCGAATCTCACCAGGGAGGTCTTGACGATGAACCAGCAGAACCAGATGCAGCAGCCGAAGCTGCCCGACGCCGACTGGGCGTACACGGTGCTCGCCGACCTGAAGCGCGTCGTCCGCGAATACGCGACGGCCGCCACGGAGTCGACCTGTCCGGAAATCCGCAAGCTGTTCACCGACCTGACGAACAGCACCCTGCAGATGCAGGGCGAGCTGTACAACGCGATGCAGGCGGCTAACATGTACGACACGTCCTCGCCGGCGCTGCGCCAGGACATCCAGAAGCAGCTGCAGACGTACCAGCAGACGCAGCAGCAGACGCAGCAGTTCATCCAGCAGCGGATGGCCGGCCAGGCCGCTCCGTTCATGCAGCAGGCCCAGCAGCAGGGCGCTCCTGCCTACAGCTGA

Protein sequences of DBSCAN-SWA_1

>NZ_CP045802|1759147:1844134|1779001_1779727_+|WP_153784697.1|DBSCAN-SWA
MSGAAAGLRKPPLRCEPAGDRALLLLPPGDGSAPPEGEPLQRLLAHAAAWLEAAGWEWLEDAVPAYESVLAVYDPARLQRGRKGAVPWRLAQRLIEDRLAELPPPPEAAERAAIEIPVRYGGEHGPDLEQAARRSGMTPSAFIAAHSKPLYRVVMLGFLPGFPYLDGLPPELAQPRLDAPRLRVPAGSVGIGGAQTGLYPSESPGGWQLIGRTAASLYDPARERPALLAPGDRVRFVPVER
>NZ_CP045802|1759147:1844134|1834785_1835250_+|WP_153783188.1|DBSCAN-SWA
MAARTAADCGSMCRHAGRWVAVLLGGGEVGVDVEEIKPLQPLFPVDCLHPAEARWWRRLPEPERLAAFYELWTLKESYVKAKGMGLSLPLHSFAVQPLEGGGAALAPPDGDCRLRLYPLAEDMRLAGCAIDGSLPSSPEFWTFEQLLERAAPRR
>NZ_CP045802|1759147:1844134|1773183_1774053_-|WP_153783167.1|DBSCAN-SWA
MIELSGVRWERRAGVFTLDVPRLLLREGITVMAGANGSGKSSLLQLLATAEFPDQGGIRYGLMSGDRDLAAIRSSIGYVPTGLELYEDMRMERLLRYLSELKGEAGRAETDRVIGLFQLEPYRRRAIKTLPQGIRQRIALAQSVIGSPDYLFLDEPLNALDSVERLRLIRFLASYARGRAVVVSTHELNEWEAWASRILWLADGKPQFHGTPQEWTSALPGSVWGGSVSPERYRELPPGDLLQVRPELDLWSVRLLAADCPGPEFAVQEPTLEDAYFLRSRARLRAASS
>NZ_CP045802|1759147:1844134|1786457_1787315_+|WP_028599905.1|DBSCAN-SWA
MNRQERLKALSEFLRSRRMALLPEEHGFPAGGRRRTPGLRREEVAQLAGVSPTWYTWLEQGRDIRVSSSVLDAVAKALRLNADEKRYMAALAGDAAEGGEPERSASDEPAALPAPLGRILDELAGCPAIVSDRRCRIAGWNEAAARVFLDFGSVPTEERNMITLLFTRPELQRLAVNWEQFVRGYLALFRYYYGRYADDDWYSRFIEAMERRDARFAPLWEESRVSAAPEVILEFRHARAGKMQFQLTSLQAQGQPDLRVSIYTPAQGTATERKMRRLMDEERGG
>NZ_CP045802|1759147:1844134|1774066_1774912_-|WP_028599909.1|DBSCAN-SWA
MELPNDKELKQLEEELRGPLSSLHARPVTASDTARLLASLQPAFDGLRPELSGRGVPDWMGGSVPDARRPTLLKLLRTQLGAYSRAYWLASLGVFLMLMYILPYGSGEEGSSMLSEVSAKLSLFLPMMFLSGLLYSFRSWNREMRTIESITPYPPALLLMARVMIVGGLNVLFGVAASLYLATRMEQFPVLPFILQWMSLILLIAGGAAYVMLRAGVKSSFVIGSLFWMAWNVMEYVLRMPESGSSAPETIRTAIYWLCLGAGALMISMAYRRSLVIKRVV
>NZ_CP045802|1759147:1844134|1763019_1763211_+|WP_153783162.1|DBSCAN-SWA
MSEGMLPVVWLLIAVALMAQPVYRLTRRIRELEDKVRELEAEVRTPSRRRNNLRMLDGGDKES
>NZ_CP045802|1759147:1844134|1779903_1784256_+|WP_153783169.1|DBSCAN-SWA
MLLGSGFPAPQGVRAQASVGGTYFTDTDNWGGGAAGSAPDGDLDYATNRISNGHALYPIELKIENVDKLPAESARLLIRAYDVDEYDGTDSTSTGEWDRIYLSDKPEDIVLGNPYTPWKTTGGWSSATASYKKEFKQSAYVGALSGANEKWNTTVLSVDPDRIKLGDQYVGASIHHYFKSSRLNAGWVTEIDWAQLVVDGGIRDKAEFSSAGITVKNGKISIDSAFLGKAGYQGPFSLEANVIQEVTDADGTVREVNLALDSKRVASVDPGEPGRWSLDLENPDIRLGEDYRINLILFEDRGGNGSNPNPGKVQHLLDIPTSEIQMLAEDFRKPSSVFAAEDFRSSFFKTNGVEGADALANGANLEKIRIASLPDPQDGELMYDGVPLSAADIGKEIAIANVSKLGFRPASTTDGEAEFGWTGFAEGKYASKPGQASFGVNRAPIVESLSKPALKGETLSFSRTDFAQASAYVDPEQQPLAAIMVTQLPDPAKGKLYLKRADAPLVPIVAGMPIAAADLDRLVFQPEAGATGTAEFRWNGSDGELYAAADKTVHIRINTPPVGADLSRTGPMGAPIGFAAPGGGSSFAALYGDEDGDAFHSAAFDLPAGFAAKGTLSYTDPSTTETVYAEPGRRTLVPALALESLRFVPAPGLANGAAVDIPWRPFDGKQLAEQPSLLRIAYDGIPRAEWIFALANEGVQELRLIPSGTDQETVTGLVYRLVPDSGPSRGTLVPDVDSDRGGWIYTPDKSFVGGTDSFRYVAVDESGQVSEPATATIIIHKALDGWAGDKPQGDPSRMTALPGYPVRLSAVSSLAAEKVTASLAGAETELVWINPSTSQAEGVKRWEKEGFLLPQAAAGEHEAAFTAYGPLGQLISNEEASRRSDNWITVLTTRIALTADPDRIVGDGSSTSVLTAAVTDESGGPVSGVSVSFAAGAGSFPDGATAVTGADGKASVVYRSAAMSGTAEQRIPVTAKVLDLVRGLAGEKGIELTFLPARIQGVLTSGSSNAPVAGAIVRAALDLNGDGVIEPGVDFEASTTTDERGRYSLAVPKGDAVYELAVTQLIEIGGVPTPVTYTQKAVVGHADGTGEQSFESEKTVSGIVLLKQPDGGTAKLDAETAGRSSVYFKDSQGKYVTDGSGAPKAHPLSAQGVFSTEGLPVGSYAFEIRYEFEPGVQAVLSVGQAHVKADGELNLLTQLVDPYGTVSDASSGAVIEGATVMLHYADTGRNKAAGKAAGSGVVLPALVGFEPNDNASPLQMTDKNGFYAYMVYPETDYYLVVSKAGYETYRSPVISVEWDIVKHDLQLRPLSAPAPQPPARTGLAVEIASEQMVVREESESLLTVTYKNSGSDRMASGTVEVVLPDGASFVRADGAAIEGAKAVWSVKDLAAGQTGQLQLTVRWPRLDAKEKDADITAAFFSGDASAKSVAKFKLYSDRFEPLFHSRYIRG
>NZ_CP045802|1759147:1844134|1763840_1765352_+|WP_153783163.1|DBSCAN-SWA
MSMKKRNDEPSGMETNRQPAPESGRGLRWTKIGPRLKLATASLLIAALLTGCGAADEGAVPGSGEAAAGGAAAVDAASRESVAGAPQKSAAKEAPTGAAAAQGSEEPSAADASAAESAELQHSDAMPPKAEPRQMPEPQAGMLTAGEWDDLGAWSRWTELIQDSPYPAAWGFAPYRRLTVQATAKGKPARDVEVILQCGGKREWTARTDGKGQATLFAGLLESRSRQDVELQNEPAASSEQQGGSKDQAAAPQDCSVQIDGGNGLLVREAEAKDWAGRVMKLETDREAAQPDAVLDLLLMIDTTGSMADELSYLSTELTNVVSRVKKNIGQNLTVRISPNFYRDHNDEYVVRSFPFLEDAVKAQAHIARQEADGGQDYPEAVAEALTDAVLEHDWSRSARARLMLLVLDAPPHQGLRERESIQHAAAEAAKQGIRIVPVAASGTDLETELLLRTLAVSTGGSYVFLTDDSGIGNGHKQPEGVEPQIMPLNDLLVDLISRHAEG
>NZ_CP045802|1759147:1844134|1759147_1760407_-|WP_101808325.1|transposase|DBSCAN-SWA
MTQYQITVDQDILHQLFIGTDRDAGVARLLETVLNQVLTAQATDQLAAQTYERTSERKGYRNGSYERDVITRAGSVTLRVPRFRDGSFSTELFARYQRSEQALVLSLMEMVINGVSTRKVTKITEELCGTEFSKSTVSHLCKQLDPAVHDWNNRSLADHAFPFITIDAIYVKVREEGRICSRGVLVGYGVNEQGRREILGLRVDDTESEESWGAYFRWLKERGLHGVELVTSDYHGGLVKAIEKEFQGVSWQRCQTHFIKNVLNAAPKALQSEIKSRVRSIFDAPDMKTARSYLEQTLEAYAETAPKAMKILEDGFEDAVAVLAFPEAYRVRLRTSNGMERLNGEIRRRETVIRIFPNRASVIRLIGAMLMEENEYWMTKKPYMDMTDFKAWKKQKATQGAGSEEQETSTTMTEATDSL
>NZ_CP045802|1759147:1844134|1819787_1820576_+|WP_153783183.1|protease|DBSCAN-SWA
MRTLRAFAEALLYVGLYAAILTLASSYLYGSGSPPTLREWLAANPNGLLLLVNPPVLLAYALLLRLQRVEAAELGLGQPPRGWAAPALSGVWLGLFIASFTGLPLVREELPAIAGLAGFVAGGSPLVFLLGSLLLGSLLEELLFRGLLLRAFRRSFGLAASVALQALLFGAVFLNVQTGLFAALGALVYGLLRAAGGSLWISLGAHLLSTASVYAAALLLRGAPASLLLILAAGSAVALALHLALTLGGGRRAAAPRLEARG
>NZ_CP045802|1759147:1844134|1840125_1841418_+|WP_153783193.1|DBSCAN-SWA
MEVMSVKSESALRPSREGALHGQPLLLLAVLTLYNGANALSGVFVPVYLFKANQSYALVGWFSLLQYAAGGLCVYLAGSWVKRKGLVASLRTGIALSGGFYMAVLLLSGKAAAWAAPLGLLNGTAGGFYWLAYNVLYFEITEKDNRDAYNGMAGLLGSAVGMAAPFLSGLVIAGSGGNKGYTVIFSVSLALFGAAALLSAKIRKRPPQGRYRWSFPAAELRQRASPWRRFAPAIVLQGLRDGVFLFVLGLAIYASTGAEQKVGTYYLVTSLVGMAAFWLCGRKLGPERRRAGMLVGTLALAAVLLPLLGGMTYSSLLLVGIGTALFSPLYLIPITSSVFDLMGRCEEAAASRVELTVLRELALTAGRLVGVLAFIYIAGRSAPDSLAFAWLLLALGAAPIAGWAFIRDRLRPEDSAVRTADPDGHARRRG
>NZ_CP045802|1759147:1844134|1762408_1763023_+|WP_153783161.1|DBSCAN-SWA
MERELQEIQGRLAAELAAALQERRLPLAPDGNPIVEERERRLDREAARLLELRERRIGEEETRLRLLALVSGLHLRNGSLNRSHELSQELDGPDGSYLHGMMHRMEGDFSNAKYWFRLAGPHPRAETWRRRTEQLLDGTPDAEPALARRLRREPGVDPALLTDLAAASALTGHAGADTPLLERVQELELELLLEALAEAGEDRS
>NZ_CP045802|1759147:1844134|1820634_1831515_+|WP_153783184.1|DBSCAN-SWA
MFDLSKLGGAAVPAPAAGMGPAAGLVSAAEAAAGGHEIAIIGFAARIGAASEPEELARLLGAADDRIGPLPETRRLELEPYLRGLGLDPLEAEFFEGAFLDDISSFDPELFRLSPKEASLMNPNQRLFLMAARQAIEQAGYGGSALGGSRTGVYVGYNADAQHDYKRMIEALCPEELGSSAPGNLSSMIAGRVAYLLDLHGPALQVDTACSSSLVAVHLACQAIRSGDCDAAVAGSVKINLLPLDSGVRLGMEASDGRARPFDDEADGTGMGDGVVALLLKPLSGALRDGDFIHGVIKGSAVGQDGSSAGITAPNALAQEDVVVRAWEDAAVDPESIAYVEAHGTGTSLGDPIEIEGLTRAFRRYTDRRQFCAVASVKSQLGHLDHAAGIAGLLRGLLAMKRGELPPNAHFRRPNRSIGFIGSPLYVNAEPAPWPRRGGPRRMGVSAFGMSGTNAHVVLEEAPEPAPVRFAEGNGRPGLLVLSARSAAGLSGYAERMLAWLATYDAQAAGLDAICGTAALGRSHERYRLAIACASAEQLALALAEALAAGLDGAAAGVEGDAGNEAERADGSGARLGANGEARWEADGMALRLRSPRLEAATAVFCGALPPAGRSLNSSSSGSPLWSGGEAAAGPAERRSSGSAVDAEEAAELARHYAEGGMPRWARLHPPGSLRRAPLPSPPLELRRCWLQPAPSARSEESRDERRNDRWNERQDAREMERREMTEQAAAAVRLTDAAADGEAEAGSAGSSRLEALQAAADAWGEALGYGELSVRSSYYELGGDSILALRTVGRLSKRLGIEVAVHELLGQPVLGDFAAMLQARLDAVRAARREAGSGGLAAAALEAPASAEPDGSSRQEPPQRPSSASSNPSQAAGSPQRPSSASSDPSQTTGSPQRPSSPLSDPSQTLGSPPEGEAPLPGFPLPAEPLPQLEAGAAEGAAAPIPLVAEQPHYAVSSSQRQMYLQQQAQPEDRSYNLPELLQLSGEVDADRLEEAIRALIRRHEPLRSSFAIVDGELRQFVHADAPFRLGRLEAEPERLDETLRALSQPFRLSQVPLLRAALVATGSNSPLLFLDLHHIASDGMSAGILLEELLTLYGGGMLPPLPLRYRDYADWQQRTLGSERLEGQRRYWRERIADDWPLLELPADFPRPPVKDGKGATFELDLEPGLAAAVKRFAAASGCTPFVVLLAAYQALLAKHAGAEDIVVGTPAAGRPSPQLERLAGMFVGTLPLRAKPAAAKTFAAFLAEVRETVLEAFAHGDVPFEELVRMDGRRDPSRSPLFDTMFIMQNLRIPDRGEKGLSYTHRRYEHGTAKYDLMVQAVERPDGLRLVVEYAVSLFREQTARTLLDRYVRLLGAFLADPERTLGEADMLSAAEREQLERFGRGPELGLPPVRAERLVEAWAAERPDGVAVIGKDGALTYRELNEQAERVAELLRREGAERGSIVAVLAERSPAMVAGMVGALKAGAAYLPLDPAAPPERIASMLQDSGACLVLTDLPEEAPARAALAGARELRLSAASAALLEADAGSAWSAASGTGAGSRSAASSWSAGGVGSRADQAGPAPAADRFSPSASASPQALPQALPQALPQALPQHLPQASADGGLLSPEDPMYVIYTSGSTGRPKGVVVPHRAFHAFAASMSRLLGGVGPDDRCLSLTSLGFDVSVCELFLPLHAGAAIVLYPDDRLLDPPRMARVIAEEGVTFAYLPPTLLGDVAGELERLAAAGAELALSRLLVGVEPIRSGVLERFAALRPGMAIVNGYGPTEAAVCATAHVFRPGGPPEAIVPIGGPMHETDIMLLGYGNAPVPPGALGELCIAGSHLALGYLGRPELTAERFVPDPRRPDRLLYRTGDLARWLPDGQAMYAGRIDRQLKIRGVRIEPAEIEARLLQLDGVREAVVDARVLPDGDKQLCAYVVLSREGGTSGLRDELKRLLPEAMLPSFLIELPRIPLTRSGKVDRQALPEPLSQAHGGVPDASGAPSTETERRIAALWRETLGVERVGRTDGFFELGGHSLKAAALAGRIRQSFGTEMPLRAVFEHPTVAGMAAWLETAASGGSAATWGIEPQAASLPGAGTERGMAAEAGRAGERALGSAHSIPRAEERPYYPMSRTQRRHYVLEWLGGGSAAYHVPLALLIRGPLDAARLEGAFHGLIARHETLRTAFVHEREEFRQIIRPEAEFRLELGRLDEEERRGLRSGPQGAAAAQAVRRRMAELLRPFRLDAPPLLRARLLEGDADRHVLLLDFHHLVTDGLSMPIVLRELLALYDGRELPPLPIRYRDYALWQERRLAEPPPGRWLERLAGELPPLELPLDRPRPAARSGRGRRLEFAFDEATSAAIAGFARGEGVTLYTALLGAYMRLLAVYGGAAEVRVGSPAAGRSHPDADGLVGLFVHTLVLRGYPAAERPLGEFLQSLQQDALEALEHQERPFEELLEALGAQPAVGRQPLFDCMFALQNMELPALEGGGLTAETLPLDAGTAKSDLLLEAAERDGRLHFQLEYDTELFADATASWIARHYAQLWKEWLRPGAASRPLEELGLIDGEERCELLGEVRQRKGEATMNKIEGAAEPERAGTESGWCSMMRQFEEQVRLRPDAPAVHAGEETWTYAELNARANRLAHALREKGVGPERLVVVMASRSPRLLAALLAVLKAGGAFLAVDPSYPEERIRWMLEDAGAAPALVEAAYAGRAAGAAEEWRLEELEEASALLPASDPEPVSRPEHLAYVLYTSGSTGRPKGAMIEHRGLASFLRQFAARLPFAAGQGVLAMAAVSFDIFLVETLLPLTLGMRVALAREEERGDAESLSRLVERHEVDVLQLTPSRFKWWAAQQGATAAFRRLSVLLIGAEPLAPSLLQRVKAATDARIFNLYGPTETTVWTSVQEVTELAADEAITIGTPIEGAHMVVLSAKLKLAPTGVIGEICIGGEGVGRGYLGHPEWSEGAFAEHPYRPGERLYRTGDLGRRLASGQFVYAGRRDHQVKIRGHRVELGEVERLAQEAPGIREAVVTAVDEEDGEQALCLYAVAEPGLEDGADERTRTYLAARLPGYMIPAYLMLLERIPLTPTGKIDRKSLPKPQARGAAAFEPPAGELERRLAGLWRDVLGQERIGRRDGFFELGGHSLKAATLASRIAREFGADVPLRELFQHSTLSAMAERIGMSAAAFEPIPRQPEREEGYPMSPAQRRLYLMQWMAGEAAMYHVPFAVDIRGALDAERLERAFGELARRQESLRTTFHYEDGEFRQKIHPPSGFALEQAPELGRLAAEELASGGGVPVQRLMKAFIRPFSLDREPPARAALLQLGPERHLLLLDLHHIATDGVSTSLLVRELGALYAGEELPEPPIGCRDFAVWQLERLESEAMREKEAYWLALYEELPPALELPLDRPRPAAPSFRGATLERRLGRELTAAAERLAAARGATLFAVLLGAYGILLAKYAGEEDIVVGTPVAGRGHPDVEPLIGMFVNTVALRLRPAGELASGDYMRGVQRDLVDALDRQDYPFERLVERLGLQAEAGRNPLFDTMFILQNMEHPEFRAGGLALEPLPFDPGVSKFDLTLEAAARDGELSVTFEYAADLFEPDTIERLARHYEEILRQLCADADGARAIEDFEVETEEAWG
>NZ_CP045802|1759147:1844134|1793097_1794702_+|WP_153783174.1|DBSCAN-SWA
MLGVLALLALLLGAPQQAAAHASLLEASPAAGSRLEAAPAEVRLVFNERIEGAVGALEVLDGSSDPVTAERAKLSEDGLTLTLPLPKLGEGVYTVSYRIISEDGHPVGGSYVFVVGDPPAARDASTFDVHAQLGHAGHEEGGLTTASLILYAVRFLYYAALMLAAGAALWPLLYRQGWSRIPEPLRGRLERLPQQALVLAALLYVFVETQQLMIGQPASEWSRLFTATAVGQSYLALLLLAFAGLALPAGRSALRFVWALPLLATEAWSGHAAAAAPRWAALSLDYVHLAFAALWAGGLMLLLVLWQAERKEAGRFAASFSRMAWISIVALTLTGIGLTLLYMTKPEYLLLTPWGILLLVKTGLVVLVAGAGFLIRVRMKRSGFPGGALLKADGALMALILVIVGIFTYISPLPANEPVGWHKMGSEMHVSIRIAPNVPGDNEFTVRIWMHKSLGDPKSVQLRLMSEDKPELGAIEIPLEPFKDDEISTFEGYTKTAYRAKGTYLPFAGRWTAEVRVMDPNDDERVERLSFRNY
>NZ_CP045802|1759147:1844134|1843503_1843728_+|WP_028599885.1|DBSCAN-SWA
MQPITGKEMEYIADSMSNEDLLAKQCACAATSISVPGVSQVLSGMASAHQQNYAMLLSTLQQHQQLAPTSPQTN
>NZ_CP045802|1759147:1844134|1842712_1843402_+|WP_153783194.1|DBSCAN-SWA
MTTVQLEDGAIEALVRARRRDLLVADDPLRGRRIYIPLHQVKGFKGAFAAESAVPAGGSRASGEVPSAQANGGKPDDDGDGAEALPTGYRAMLLEAKGTFAEVRLSARQALHGYLAGVMNDFALFCTPLHGAVLLPLQHVQALSPYPAGLAPYRLEPEQFPIRPLSLGLSRHFEQQLERLEGEMTVLCRGFLPDVAGVLGPVRDGFVPVTEADGGRLLLPVSALRAVFL
>NZ_CP045802|1759147:1844134|1763403_1763706_-|WP_028599914.1|DBSCAN-SWA
METYPLLLLTLTHGGWTKELEMESAELALVTDAGSRLWYIDVNGVADSELLDYFYTASDIGVEVSALTKDGRRLEGTAYFHANKLHRAAALRGDGELIGV
>NZ_CP045802|1759147:1844134|1805586_1816182_+|WP_153783179.1|DBSCAN-SWA
MDSFLTLTGLLAARRRDASGIVFAEPSGERFLPYAELESRALGCLVSLRRRGLRPGRHVVLQTESNASFLELFWASLLGGAVPVPLAAARTDEQRRKLAAVLAQLPAPLVLADADLAEAAGGADVIQIAELEPAADGGTTQPHRADPDEPAFIQFTSGSTGDPKGVVLTHANLLANMRGIVDGARSGPGDSSLSWLPLTHDMGLIGFHLSPLLAGMTQWLMPTSQFVLRPMSWLELASRERITCLASPNFGLLHLLQHFKPEQATGWNLSAVRLLFNGAEPISADACRSFLERLAPYGLRPQALFPVYGLAEACLAVTFPDPDERLRTVHVRRGRLRPGEPVPFAAAGDPQAMELVELGSSVAGCEAALFDELGRRLGEDEAGLVCIRGLNVTGGYYNRPDVNEALIRDGWLNTGDIGFFHGGRLYLTGRVKDILLVNGQNYYPHDLEELLAELPACAAGKAAVCAVADPASGSEAAAVFVQHRGKPESFLDIRRSVRVLLSRRAGLEAGPVIPVKRIPKTTSGKIKRFELADELLAGRFDEALAALEAAEAAALAAAAADMPSAAADASSAAADASLAVADASLAAADASPAKGAPPSASAETAAEEERPAPAIGAGAGEPRGETGKQPPSLSQEETATERRLLAIWRELLGTERLGRDDSFLEHGGNSLRAALAAARIQEELETPLPLTELLRHDTARSLAAFIEERKAEGARIEPPAEPIRRRMRAGYPATPAQRRLHVHEQLYPGSLSYQLPYEIAVDGPLDDDRLRRAWQELLARHDALRTSFRVAEDGVLVAEIADRAELPLATVDLTGLAPQEAEAAAAERARAFPRPMELERAPLLRLELLLLPEGRRRLLLDLHHLVTDGSSMGVLMQELAALYDGRPLPEPAPGIGDIAEREREEEGGAAAERSRRYWRDRFLSGVPAAAFPADRLRPARPTFRGRSERLALGPELTDGLGRLARRAGTTLYGALLAVYGVLLERYAGEDDAVVGTAYARRTRRETVGTVGLLATLLPLRLTGSRESSVLDWVRTAGEAAAEAIEHGAIGYEAIVEAVGAAREPGRAALFDTAFTLQNVELPEFRTEELALRPAMIETGSCKFDLFWECELGPEGLSIRLEYAEDLFDGETARQLLRHYAQLAREAALDPLRPAASLPLMDEEERALLLRRGLSRWPEKDAVPLQERIGRHALASPERIAVSFAGGSWTYGRLWEASGRVAAALSALGLGRGSRIAIAMGRSPQQLAALLASLRIGGAYVPIDPGYPAERAAFMLADAEADILLADEAALPLCRQAIAACGRAVRLIEAETLAGRCPSSSSPDSPLPRTASAGPAGEAAERAESFVSPDDLAYILYTSGSTGRPKGIRTTHRNVARVVDRPGYVEIGQDDVLLQLSSYAFDGSTFDIYGALTNGARLVLAGSDEAMDAPALVRRLREEGVTVLFATTALFNTLAAYGLDGLPRLRKLLFGGERASVSHALKALAALGPDSLLHVYGPTETTVFATAWPVRPPAPGAASLPIGWPVDGTEALVLDACGRLAPDLVPGELHVAGGGVAAGYVGLPRETEARFMPHPFRAGERMYRTGDLVRRLRDGSLEFLDRLDQQVKLRGFRIELGEIEARLLASGQAEEAYVGLVGEPPRAELCAYVVAAPERFDAASLRRWMAGGLPPFMLPAHLVRLDRLPLGPTGKVDRKALPLPQPGDAAGSAGAERERPATASERELAELWREALGRADVGVLDSFFELGGHSLTAAALTGLIHRRLGVRMPVREVFARPTIREQATWLDKAERSGREPLLPAAPAESYPLHPAQARLALLERQGGIGLAYHVPLALRLVGSPGPEAVLAALQALVDRHEPLRTEVRDAGGEPRAFVLAQAEVRLERMRIAGEEALPGAMKSFLRPLPLDAAPPLAACYAEGGQGESFLLLNLHHLAVDGVSVGLLLEELVRLLEGGLPEPAPTVQFKDYAAWLDAGFARSEASVDSPDAGGSARSEASVDLPDAGGSARSEASGDLPDAGSSARSEASAAWWREQLAAPLPQPELPLDRPRGASRSFEGGLLAFDFPEGLTDGLEALAARCGVTLNSLLFTLYGALLARWTGAEELMIGALGAGRSHPDTGSMIGMFNSFLPIRVALPRGLPLERAARDVQERLLSAIEHQELPLERLLELAGGPFDPARNPLFDTMLVLHSQFGGELAVRGSRCALEPVRWGGAGTAKLDLKLDLYGDGPHGLRGELEYAAALLQPQTVRRLAETWIELLQRAVREPHAELGVLMRLTGSEARLLEQWNATTAAYPDRSTLHGLFAEQARRSPDRPAVRSAEGVWTYRELDRVSSRIAVRLRAAGAGRDAIVAVAARRSLAMMAGLLAVLKAGAAYLPIDPDQPPERLRDIADDSGCGLLLASRGACMELADAEPRRLRLELETLVAEALAAEASAPGELLPELDAAAEASPESLAYVIYTSGSTGRPKGVLIEHRAIVNRLSWMQRAYPLTEDDVILHKTPATFDVSVWELFWWSLAGASVHLLEPGGEKDPSLLLRAIREQGITTMHFVPSMLGTFLPYAAAFGGSRPLAGLRLVFASGEALKPAHAAQLAQLRPAGSPLPRLVNLYGPTEAAVDVSHYDCAEYGGGPLPIGRPIDNIALHVLDERLQPLPPGAPGELCIAGAGLARGYLNRPELTAEKFAALADGTRVYRTGDEARWLADGSLEYRGRFDHQVKLRGQRIECGEIEQAAMDVPGVLDAVAMLADDPLGEPQLCLYVACGLTEPERAELAARTLPQRLARRLPDYMLPARFVALESFPLTPSGKTDRKRLPAPDWSGGAPTGRPPAGEAERRLAELWTELLGVRDLTAETHFFRAGGHSLRAAQLAGAIERTFGVRFSLRDVFEAPVLEEMALRVGRAEASGSPPLPSAGERGHYPLTPAQNRLFILHRLDPDGIAYNLPLGLRLEGELDEERLQRALRRLVERHEALRTRFGWSDGHPVQIVERDVVLTAERLAGTLEEASAGFVRPFDLTQAPLLRAGLLRDERGGALLLDMHHIVSDGLSLNALARDFAAFYDGREPEPLALRLVDAAVWQRSWLETPERERQERYWKSKLAGPLPALDLPLAAPRPDRPDGRGSRVARMLPEPVRRSALRLAEQLEATPYQVLLAAYAALLYRMTGEEDLIVGTPAGGRFHPDLQPVVGMFVQTLPLRLPAAGASSFRELVAAAGRASVEAMDHGQLPFELLAASLGAGRDPSRNPVFDTMFVWQNMEPPVREAGGLRLEPFRLRQDAAKLDLTFELAEREEGVELTVEYASALLTEEDASRMAGWYVALLEAACADAGRPLAELPLLTAAEEREQERRFQPADSIATGPAEPGFAAAAEPATLDGVLRRQARLAPEALAVSSAHGSLTYRQLDEASNRLARELLARGVAAEALVAVCMERRPELIVAIYGILKAGAAYVPLSPSLPAERIAYMLADSGAPLVLTAGDVRLPEGRRRRASTSRRRSAATTIRRRRRPATAEAAWPMCSTPPARPDGRRASWSSTAPC
>NZ_CP045802|1759147:1844134|1799040_1801476_+|WP_153783176.1|tRNA|DBSCAN-SWA
MKISTNWLADYISLEGLTPQEIAEKMTSGGIEIDAVEAMDKGVSGVVVGYVKEKTKHPDADKLNVCKVDVGAGEDLQIVCGAANVDAGQHVPVATVGAKLPGGLAIKRAKLRGVESQGMICSARELGLNDKLLPKELQEGILVLPKLELGRPIVDVLDLGAHVLELDLTPNRSDALSYLGVAYEIGALTGRPVKLPESAVFGAADKTADRLSVRIDAREACAHYSARYIRGVQVAPSPLWLQNRLMAAGIRPINNIVDVTNYVMLEYGQPLHAFDADRVAGGSIVVRFAREGEELETLDGQLRKLQPHMLVIADGDRAIGLAGVMGGANSEVDGDTTNVILESAKFDGSVVRRTSRQLGLRSEASLRFEKEVDPARVIPALDRAASLIAKLGSGLVTDGIAEDVARTYEPAVIEVSLERISGYLGADISKLEAQAIFGRLGFDSEVGDGSIRVEVPTRRGDISRDVDLIEEIARLYGYDNIKATPIVGETTPGSLTAPQAVRRELRRRLSDAGLHEVISYSFTAPERAGLFPDLAQDAKPIRLAMPMSEERSVLRTSLLPQLLETAAYNRNRKNHDLALFEIGTVFHTDEETLTRLPQEKHRFALLLTGASRSAAWNRKAEKADFYDAKGVLETIFAALGLSGSVSYEAAAPSGLHPGRTAAVKLDGERGAETIGYVGQLHPELQLELGLDDVFVAELELGALYDAADRSIVYRTLPRYPAADRDIAVTVDETVPAAALAAAVREAAGELLESVRVFDVYTGEKLGAGRKSVALALVYRHAERTLTDEEVAAAHAAAVAALEQSFSAELRK
>NZ_CP045802|1759147:1844134|1841367_1842489_-|WP_052333442.1|DBSCAN-SWA
MRAGLAVRSIRISAQAQADLASDVWSRKHVPVQLTTGGRTDGARLRYRGGHTREYPKKSYEIRLDSGLVLHWNAEADDPSMIRNALSFRFMEGIGVPAPRTRHVWLDVNGECRGLYLEIEAVNSRFFALRGIPYRSLLYAANDSANFERSLSESGRRKRDLAEGYEFIEGDGETLPRLCSFIRGIHRLKNAKLRELLEERLDVPAYFRWLSGAVLTGNFDGFEQNYALYEEATRQQYGILPWDYEGTWGRNCYGKLCPAGMVRVQGYNGLTRRLLQFDEWKRAYAEGLERILEEDFTEERIGRLVEELHGGIAAAVRHDASRAANRGLFGGEPEVILQYVRQRRASAAKELRRWTRGSSAPAGMPVRIRGTDG
>NZ_CP045802|1759147:1844134|1777748_1778624_-|WP_028599907.1|DBSCAN-SWA
MLTACKLGKQYKTGWALRPLTLELGPGLHGLLGPNGAGKSTLLRLLAGMLAPTTGDALLRGSSVRDFRRSGSRIGYLPQNIRVLPQFSARQWLLHAASLQGGGSLAERRRKVDEVLEQVNLLGEADLPARHYSYGMTKRLGVAQALLSAGDLLIVDEPTAGLDPEERIRLRRVLAEAAATRVVLLSTHVLGDIGASCREVIVLGEGRLLYHGSTQGLAGFAEDRTWAWETSENEWRRMPLGGLLSARRTEEGILCRALSDRPPSPFAERVEPTLEEGYLSLMNRQPSGGPT
>NZ_CP045802|1759147:1844134|1818124_1818991_+|WP_153783181.1|protease|DBSCAN-SWA
MKKIAFAIARIAFYLGVFYALLYGLNHLYRIDWTAPFVELLGRNPALFMATLFASITLVYALAFAGVRRLTRGGSPSLAEAAGLHRLPAGAALGCALIGVLGCLFSIGLIEIPAVAEAYPSIPALVDDLLRGDHLLLAILGAGLVAPAYEELLFRGLILRELRGMMPAAAALLLQALAYAYFQPSPALSVIGFGSGLLYGYLRISLNSLWAPILVQITAMSLIFAAKPAGVYEAVGSLGGAGAASVAAGSLLLMLAAAGWLRLRYASRQRLADAAGERANLRERTVQG
>NZ_CP045802|1759147:1844134|1833282_1834536_+|WP_153783187.1|DBSCAN-SWA
MRKRPAPALLFPGQGSQRPGMGRALLERHAEARAAVEEAGDAIGADLARLLRDGSMEELTRTEIAQPAILAVSVAMYRVYRGSLGGPPPGWLAGHSLGEFSALACAGALPLGDAARLVQARGRLMAEAARRQPGGMAAALGIAPERAEAICREIAADGRFGVVVPANYNAAAQTVLSGHFPALEEAARLVREAGGSTVRLAVGGAFHSPLMASAAAAFGEELSAARLGSPLLPVLSGVTGRRMPGSAAALAELLQRQLTAPVRWTAVMAKLAELGARAAVEAGPGAVLQRLAAGSGIRVLAMDEEAALGELEETLRRGRCLSYLEGCLAVAVGTRSEEDDLLVYRREVEAPYRELEQLLQAAEAEPSAPVDAARLEQAESLLGRLLAGKGLPEAERRERLSRLAAAHGRRPVEAEAR
>NZ_CP045802|1759147:1844134|1784322_1784853_+|WP_153783170.1|DBSCAN-SWA
MSDGPADDAKAGSFRDIRSGHWAEGYIRESAAKGYFKGGTDGRFRPDAPVTRAELVVVLSRFLGLEPGEPAGSRFLDTAGHWAEKEIEALRVGKYLNGYPDGSFRPNQPIRRDEAVALINGMLRRGPLAGVQPLFPDMPQGNWAYGAVMEASLSHESERVEDGSERLLKAIEDHME
>NZ_CP045802|1759147:1844134|1838861_1839278_+|WP_153783191.1|DBSCAN-SWA
MSGIIDGLLGNAYASSLIYVAVTIMALILFLTLFEWVAKYKCWDEIRKGNVAVAMATGGKIFGICNIFRFSADAGDSIYGSLIWGTFGFVVLLLAYFLFEFMTPVFRIDDEIQRDNRAVGLIALIISVSISYVIGATI
>NZ_CP045802|1759147:1844134|1832464_1833286_+|WP_153783186.1|DBSCAN-SWA
MEPARGRGMRPLRLFCLPHAGGSAQLYRRWAAGAPPGLELAPLELAGRGVRLGEPFYLGIREAAEDLLGEVLERREEGRFALFGHSMGALIAYELAVLLQRAGGPQPEAAFLSAKDAPQVERREAPIHGLPEEQFIERIRRLGGCPDELFEQPELLRLFLPVLRADFRLVETYRHQDAPLLETPGVVMGGRADGTLSGSWVEWQRWFAAPCRLELFEGGHFYAQERHPELLRRIADILGLAPERGGAALAPLASGAGGGRLGLGGIGEGRNSR
>NZ_CP045802|1759147:1844134|1835939_1836296_-|WP_153783190.1|holin|DBSCAN-SWA
MNFLGHVVRFIVSAIVLMLVGFIVPQFTVGGFWSALMLALVIALLGWVVEGIFGKRVSPFGRGIVGFVASVIVLYIAQFIVGGVAVTWLGAILAALVIGIIDLFIPTPFDAAKRKEQH
>NZ_CP045802|1759147:1844134|1769862_1773102_+|WP_153783166.1|DBSCAN-SWA
MKKWGSLLLVIAMLFTAVPTAFGAVRTGWDLKSPRGIATDSSGRIYVADIGNHRIQVFNENESLSMTLGETGIRGADNAHLDTPTTVAVDAATGEIYVTDTSNKRIQVYSSQGSYLRSLALPASAVSESVALDGLGHVFVTDHNNMIYRFNTDGSGYKQLFGYPDVDYRPLGIAADSKGTLYISQVLRNTIVVYTYNKSQDKYTYQKTIGEKDKPGTDNMHFNQPWGAHVDRDDRLYIADGGNKRVQVYNSDGSYHMTLTAPSLTSPYHVATDRNGTIYVSDNHRSILMFDAQGQFVKTLGQNTVPVFEGSQTALAVAQDSSPTDVRSLLKVTDSDSGQTLSWTLTTAPTHGAVSLGQGVAASGGSGLTPADAIEYEPAAGYFGTDQFTVTVSDGAGGSAARTINVTVSRKAAAPTADPASGSVVADGSGIALSTTTPGASIYYTTDGTEPTTASAAGTAVAVSGAPGETVTVKAFAAGPNLLDSDVVTFSYVIETPKSSNADLQSLSLSAGDLSPAFSSGTTRYSASVASEISSLTVTPSVADAVYGTVAVSVYDGTGKLTGGPHALSGGGASPALPLAAGDNVIEIRVSAQDGSMLIYTVSVQRAQATETPQPEQPTEEPTPTPTPVESSTPTPTPVETPTPTPTATPTPTATPTASPGLSMTVNGQPKGQLVQAATEQTNGQTILVASVNRAQLLEQLAAAADGAVMAIPAANEPVDGVSVRLTGDVVQAMAARKAQLQVQAPSGTYALPAGQIDIASLAARFGAADRLSEILLRIDVVQSDAATAELARQAGLRQGFHVAAAPVTFEAAAAFDGKSVAIDRFSSYVKRELPLPQGADPAKITTAVVIGKDGTVRHVPTFIEMRDGAQYAIVNSLTNSAYALVYHPAAFADVAGHWAEPAVNDLASRMVVSGVDAEHYRPDAAVTRAEIASILVRALGLAPSSAASPFADVDAAAWHAGSITAAQAYGLVQGDGHGSFNPSRSVTREEALTMLARAMAIAGMDASGAGADSLAAHRDGGQVSLWAQDAFAAALRHGLVQGSGKGLEPKRPITRAETAALVQRLLIAAGLIDQAGSK
>NZ_CP045802|1759147:1844134|1818987_1819791_+|WP_153783182.1|protease|DBSCAN-SWA
MNKWKDGLLRPVVIIGIYFAWFFTVTTLFFDYVYRDTAWFQKNTLVTILLNDIVGLPLMIGAIWLLFRQNLFREARFRRIEPTSVLICVWIGLGAGLFTAAFSQLPLIRSSDYQFQTLFDYINRADWYVFLGFLLLGNVYKETLFRGLLLNSFRRLMPVWAAIALQGALYGALFFLGDVPLSLYGFLGAVLFGLLYVRLDSIWAPIAAQIACQGLQYALWHYAPDLGGAAALSVIMAASLAMIAAGVLLLFKRQPAEKAPAGRTASA
>NZ_CP045802|1759147:1844134|1761448_1762387_+|WP_153783160.1|DBSCAN-SWA
MTKMRERNDWNVAHGMEERWRELRFGLEIEFVGGEPERLELLPGWTMALDEKQIDGDGEASGSELQSPPLRWEELDQAEAMLERLRRQGAQANWSCGLHVHVGLEPFGEAALPALLEAALSSQEALSSLLGTSPHRRFYAPPITAEMAEAFRASGDLAALRRSGRPQSHRCGINLRPWSEIGTVEIRYANGTLEAAEVRRVVELCLRFVDGACRGQRMPDEPAALAAALGAPSGGYPPRADPPRWHRERIALENALLPQLAAQAAELVPGGEIHHIVAADGGVMVAVEDEEGSLHRFRCALAAGGLEPLGDG
>NZ_CP045802|1759147:1844134|1789438_1790206_+|WP_153783172.1|DBSCAN-SWA
MQKPTIDLNADFGEGYGSYAFGDDAALLGSITSASIACGWHAGDARTMRTSVERCLRAGVAVGAHPGYPDRQGFGRRAMALDAEEVYEAVLYQTGALQAFVRAAGGELRHIKPHGAMYHRCGASQAHADAVARAAAELGGLALFGPPGGLLERAAVSAGLPFAAEGFADRAYLPDGSLAGRDRPGAVHGEPSQALEQALTIALRGEAPALGGGFAPVAARTLCLHGDGPGAAELAALIRAGLEAAGVAVRAPWQP
>NZ_CP045802|1759147:1844134|1796589_1797315_+|WP_153784698.1|DBSCAN-SWA
MSRSKGSVAALLAALSLFLMAGMASAHVTVWPKEVAQNSYEVFTVRVPSEKKDVLTTAVAVRVPEGVNITRTQPQPGWKTELERSADGKIERITWTAEEGQGLAVENFTEFKLSGKVEADATELKWKAYQTYSDSSVVEWIGAPDADYPGPVTAVGAGEAESDGHGHGAAEASPAPSSAPDASAAPEASAAPAASDAPAVDQPLAPAAEKDSLPLILSIIALALGVVAVIAAFTRRGGSKG
>NZ_CP045802|1759147:1844134|1774892_1775483_-|WP_052333479.1|DBSCAN-SWA
MTDEELVQGMMDGDQASFEALVHRYHAPLSGFLQRQLKDPGRAEDIVQETFLKLIRQLKDRRSPDNVQAWLYRVAMNQCRDYWKSSGYQTDRNRFGEPPERKDERPSVVEMAERSETRREIRQTLEELPQVQREVVLLRFYQDLKLQDIADALQLPLGSVKTHLYKALRRLKTKLGKEQKAPMRAEGGEPDGIAER
>NZ_CP045802|1759147:1844134|1816115_1818128_+|WP_153783180.1|DBSCAN-SWA
MLYTSGSTGRPKGVMVEHRSVLNRLRWMQRAYPLAPQDVILQKTPVTFDVSVWELMWWSFAGASAHLLEPGGEKDPSAIARAVAEAGVTTMHFVPSMLHLFLEDAAARQAARAGSLATLRTVFASGEALGASLAERFEARIRSACGAELVNLYGPTEATVDVAFYNCSREGLRGGGVPIGRPIDRTALYVASPGLRMQPPGVPGELCIAGIGLARGYLGRDELTREKFVPNPFRGGGRLYRTGDLARWLPDGQLEYLGRLDHQVKLRGYRIECGEIEAALQRDPRIGEAAVLLRRRAGDEGADYLCAYYTAAAVLPKRELREALARELPDYMIPAAFVRLERMPLSPSGKTDRRALPEPQPADPAGEVRERPGTETERAVSALWGELLGGGEPDVRRSFFEAGGDSLLLLRLHQRLEERYPGALQVADLFSYPTVRKLAARIDSRSGDDAVLEGPVVALPGEPPQTVRSGPREGRLDIELEPAAAAALAAMAQERGARLESALLGLYLLHWSRTAGAERIGVAATVGQGRITVWNADFRELASMEQLLDAAEAALASGVGIPAERIRRVRPSAGRWSAAPLFRLESPETPLPPAGELLDRFDHQLSVWAGEPGLPLRCSWTYAARQFPAELVRGWASGYAELLRGAAALYREAAASRPDEQDQGKGIISS
>NZ_CP045802|1759147:1844134|1791257_1791425_-|WP_153783173.1|DBSCAN-SWA
MSKSQPFEPYRYAELPLVAVERIRELEQSLSDGEGRPVTLIAFEPEPESQAPNAR
>NZ_CP045802|1759147:1844134|1790676_1791063_+|WP_028599902.1|DBSCAN-SWA
MSPSSGIWMFVYGTLQPGRSNFGVVAPFVLAQRPGRVRGRLVDAADGHYPALVRELSALNRAVRGWWLLLERDGLAACDRLEEFFGPEEANDYERIWTRDLDDPARQGWVYVWPDDRGCADLHNGVWP
>NZ_CP045802|1759147:1844134|1775493_1777752_-|WP_153783168.1|DBSCAN-SWA
MIPNVLRQAAMELRSLLLLRWTLLLPAAASIWMLLHTWRLRPESSQDINLYASDTHQMLLMLTTAIPLLLGVLLMRRDLLHPSAEWLFRLPLPAGGWMAAKWLAGLAYMTLYTLAVGAAYAASALRHGLPAASMGRQLALYGLLYEHAFAVSLALGLFLGVLLPLRFSLPAAFCAWVFGSLFLQAYIRPVYEWSWLKAFYLQPLFENSLLGNEVWSWPLARGELLRIMGFGAAFSLFLLVAGAALLGRSKPPLNRRRPWLLALVAMLAAAGAFAPFASLEAARDVHRAQLEQAAAGPDERLDPAAYRFRLERMDLRLKLAGDGSLVAEATLELPTEKGRLLPAERGRTLRYKEPGIVSLLLYPSLQVRSVQLNGVPIAWERKGDSIRFPELMLDRGRPVQTVEIRYGGRLDEWLSGPGGSESYLAFLRSDALYLPASLGWYPLPGGDTLLALDEDGRLLDRPSSALTPGTAYEVEASGFRAPLFGTLPEEPSADGAVRFRGVSGAGLTLVGGRFETVRREGEAIRIVTTPGNRDEAEAFLERFERRREGLEELAGAPLGAVRQLFFFPMHLIGAPVEAPSVNRSWHAENDTLFIPQTEHRNLDGYAEDALSDLLLFGDVGRGEAMARENALEDPSGSESVALAIRSAYAFLYNKQRGPDEPYRIEAEELPAWRSMRALIQAAYDRGHAALAREVLEQFRSRGLALPEPPRSGAGERMAAAAPPYVTVDEFMKEWRARMPDDRWPPMTDDEGG
>NZ_CP045802|1759147:1844134|1805188_1805572_+|WP_153783178.1|DBSCAN-SWA
MFREIHKSKIHRAAVTEANLHYVGSITIDQDLLDATDIWENEKVQVVNINNGSRLETYVIPGPRGSGVICLNGAAARHAQPGDLVIIMSYAMMAEEEARGYVPKVIVLDADNRIASASYRELHSTTI
>NZ_CP045802|1759147:1844134|1797983_1799018_+|WP_153783175.1|tRNA|DBSCAN-SWA
MKERLEALQAEALQELQGVAGPQELGELRIKYLGKKGALTEILRGMGALNAEERPAVGEVANRVRGAIEAVIEEKAAAYRRAETELRLRSETIDVTLPGSALPTGAVHPLNKVAQEIEDIFIGLGYTIAEGPEVETDYYNFEALNLPKNHPARDMQDSFYITDEILMRTQTSPVQIRAMKAMNGKSPLKVICPGKVYRRDDDDATHSFQFNQVEGLVVGKGIRMSDLKGTLLQFVQEMFGKQARIRLRPSFFPFTEPSAEVDVTCSQCGGSGCRMCKQTGWLEILGCGMVHPKVLEAGGYDPEEVTGFAFGMGIERIALLKYGIDDIRHFYANDLRFLSQFERM
>NZ_CP045802|1759147:1844134|1843756_1844134_+|WP_028599884.1|coat|DBSCAN-SWA
MNQQNQMQQPKLPDADWAYTVLADLKRVVREYATAATESTCPEIRKLFTDLTNSTLQMQGELYNAMQAANMYDTSSPALRQDIQKQLQTYQQTQQQTQQFIQQRMAGQAAPFMQQAQQQGAPAYS
>NZ_CP045802|1759147:1844134|1836476_1838840_+|WP_028599889.1|DBSCAN-SWA
MDSKILSTLEYSKIIHQLIQHTATPMGLRMAEELAPSSALEDVVRSLQATAEAANAYRLKGNPPFRGVADIRAHLKRAAIGGTLSPGELLEVALTARGARRVRSHVLHLHEEHPMPLLALLAEGMYPRRELEDEILACIDESAEVLDGASVELGRIRRELRQGEGRVREKLEQMLRSSSVQKMLQDTLVTLRGDRYVIPVKQEYRSHFGGIVHDQSNSGATLFIEPEAVVALNNKLREVKAAEAREIERILQKLTALAAEAAEDLAINHDGLAQLDFAFAKAQLAHAMKAELPLMNDEGRIVLKRGFHPLLDRTKAVPLHLELGSSHSGIIVTGPNTGGKTVALKTVGLLSLMAMSGLFVPADDGTELCVFDAIYADIGDEQSIEQSLSTFSSHMTNIIRILRDMTPSSLVLLDELGAGTDPAEGSALAIAILDHIHRTGCRLLATTHYSELKAYAYNRPGLINASMEFDVATLSPTYRLLVGVPGRSNAFAIAERLGLSKAIIQQARGEVSEEDLRVENMIESLERDRQRAEQERDSAEQLRRELEEERSLYEEELRRFEEQRERLLAKAQEEARQAVQKARREADEIIQELRQLQREEGAAVKDHKLTEARKRLEEASPQLVKGRQGARPAAAERAIEPGDEVKVHSLGQRGHVVELSGSEATVQLGILKMKVKLADLELLKPAPAPKAAPKAASSTLKRTRDDNVKMELDLRGSNLDESIIEVDRFLDESFLAGMGQVYIIHGKGTGVLRAGIQDFLRRHSHVKSYRLGNYGEGGAGVTVAELK
>NZ_CP045802|1759147:1844134|1794765_1795632_+|WP_028599900.1|DBSCAN-SWA
MKASTIKRLILWTPTVLTAAWEYARHTFLLPYVSMDTGNVISPILVFLVTVTLLSKLFAMLENVQEQLRREQAVKAAVQERDQMARELHDGISQSLFLLSVKLDRLDRAESPEEVKQASEQIRGTVRHVYEDVREAIASLRSADTAAESGMPWLQPLQDAAAELEESGTSTEIDWQLPDLLLTSREKVELLAIVREALMNVRKHASASLVSVACRQVGADGFRCVVADDGLGASPGAESAKGHYGVRMMRDRAEGAGWSFRFQSPRPDLETGTSVEIMRQPSDAKLKP
>NZ_CP045802|1759147:1844134|1768578_1769688_+|WP_153783165.1|DBSCAN-SWA
MRAILIDDEEIALDVLEIKLNEAGGVDVVGKFQRVADAISQCGALQPELLFLDIEMPGMNGLEAAAALRAVCPDAEVIYVTAYHHYAVDAFGTEAIGYLLKPVAKDKLLQALSRYESLRARLRDRSGAGQEPSGATTGRTGTGQASPLDLVPPPDSPTLSLKVLGSMELYGGDGRLLTWRTRKTKELFAYLWHHRGRPVYKYAILEHLWPDDSAERAQKLLHTSLYYLRSLLKAEGCGEIVHYGDERYWLDAGGIRSDLEELLERSKTGLEGEAGQDAAGLYRGDYLETEHYPWADAYRIELRSSFTAALRAGLVQAGSAQRLALLGKLIELEPEHGPYYDLLAESQEQMGHWSGARQALALKERMGRE
>NZ_CP045802|1759147:1844134|1788808_1789417_+|WP_153783171.1|DBSCAN-SWA
MTNDQPGVDPQAASSAKSGKRKGAPAFVAGLYTADAPGSFVSRELAEAELEFGGIRGDRHFGVTSRADSRQPMYPRGTEILNRRQISILSREELEETRERMGIEALDPEWIGGNLLLSGYPGLTQLPAGSRLLFPSGAGLVCEGENHPCTDAGKEVERHVAPKERLPQAFVKAARGRRGIVCSVERPGRIAFGDEIRIIPPM
>NZ_CP045802|1759147:1844134|1839411_1840008_+|WP_153783192.1|DBSCAN-SWA
MEHQQQEGAADICPWCDSELVWDEEIGPEEVCPHCSNELGGYRTLSVGGAQAEEEDEDEGAGLAAGHAGAAARTAGAASRSVEGLDEEADWEAGDDTGWAGAGRPQSWLRADEKVQRILDDQEEMPECPSCREYMLHAGTNALGAGSFSPVEPPSLKKPLLPDSIRLQLYVCPNCHEVSTKLDLGSRTFLAERLDQED
>NZ_CP045802|1759147:1844134|1801676_1804709_+|WP_153783177.1|DBSCAN-SWA
MKEADRLRVTVDIYGHQYRLTGHSSSDYIRRVAQVVDENMHKLAKGYPRLDMPRLAVLAAVHMAEDVFRLRQDSELLKEEQSIRKTLMGELDKAQAATEQAREELARSERRAAEELERLLGEREAAEAALRAEAEERLAAVQEAVKEEAQRLERQSAETAAELERRWREERERLIEENRVRAEELERRHEAERAEAAQMLEAERQEWERLYEAEANERESRLAEAMAEAERRHEAEKAAAREQLETERRRLAVQLEESRAELERRLEEERAEAAGVFERERAELAAAHAAEMAAREEAFAVQLAELEERLLERIHELQALHAGEAEARERERAELEQLYEAECREREQERAALLESKRAELETLEARHLLRVGELEEQLLAARQQGERSLAELRLQQRAELEGALAGREAEHRGELERLRAEQELQLAEALELAQATEAELQSQLTESASALEEARLQLAALEQRLQQQRQEQQRQLQELQQEQLQVLQELRQEQQQALEAERQQLQERQQELEAEQQQLQAERERGSRLELKLAAERTGREEAERLFAEAGERAEALERGEAEARERLGLAEEQLEASRRELEAQAGRAAALEAELERLRAASAAEREAAASELREALERAAGEIGHAREQAQAEAAEQVRAAERRAEALQASAAEEAERLRREAGEELELAQLAAQEERERLAAAHAQERERLAAAHAQELERLRAAAEAERIGGAERLRELEERAAGEAGRAEEAQSRLAGQGEQWARERSGLEQERDAARRELAEARDDWSKRIADAEEHLMLVMEQEEARGRLLGESQRLLRSTQEELELSRQRTAELDDRLRETASRLQEAVASRDEAEAALRERLAAAEAAREALERRLSEMTGQAEALREQSERDWQRQLDEAAAERERLSRLVAEQQERLEQQSRLEADRAEAEEELRRQLELAHREAAVSGSAVERLEDAMRQLEEERTDSRQDLGELQRDNERLTTAYDKLRTEFELLRTEYSKLQTEYNEWIELIEQS
>NZ_CP045802|1759147:1844134|1785050_1786343_-|WP_101808824.1|DBSCAN-SWA
MELYTNAAPSSKEHRVVITGMGAVSPFGAGAETLWTAQAEGRSGIRRLQEGGWPEEWLEQADERAIAGLVPDWDGEARFGRKEARKMDRFVQFALAAAEEALGQAGLGEGRLVPDRTAVYVGSGIGGLGTLMEQARVLGARGHSRVSPTLVPMMIANMAAAEISIRYSLTGPTLSPVTACSIGNTAIGEAMRLLRAGIADVSVAGGSEAAVVPIALAGFGNATALASSGGDPAAASRPFSRSRSGFVMAEGAGIIVLETLAHALARGAEPLAEVLGYGATSDAYHRVATEPTGRGAAAAMRLALADAGLEAERVDLVCAHATGTPAGDLSESRAIRSALGERGGSVPVFAGKSMTGHMLGASGGAQAITLVRMLREGLIAPTLNQEEPDPDCALTVPAAPRRERLAVGLSNSFGFGGHNAVIALGRFEEG
>NZ_CP045802|1759147:1844134|1835379_1835775_-|WP_153783189.1|DBSCAN-SWA
MNRSFFRRLPLIAAAAGFLLISAACGSSSAPASNGPSAAVETTAEPTQDLVIKATNYKFDQESYTIKKGEPLRIKLESDGIHGIRVANTSVKMNAGDEKVYSFSEAGEYQIECSIPCGPGHEKMISVLKVV
>NZ_CP045802|1759147:1844134|1765528_1768582_+|WP_153783164.1|DBSCAN-SWA
MKNQLLLLVGLVLIFAAAASIVVYYWLHPVENYPQARAGVLDARDWDFTKQGVIPLQGEWEFYEDRLLTPADFAQSEKELESGRSLLNVPGNWNSADGFGAGTYRLRIEVSEPGYYSVRAKKIRLSSRIYAAGDELGGSGTPAADPSRFVPSNLPVLGTVKAESRTIDIVIQVASYRYLPGGLVQPPEFGLAEEVAARRDVSRMGDMILVTALLVFGLYFAGMFRQWRREPYLLYFSLFCLSLGLFFSIDNEIVLASLLPSISFPALQKLLFIVPSLSILFFIHYVRLYLDDKPGRGLKAFLGASYGFLAVLIFIPNEGLVPLLWPGILMQTLSFVFIFTSIFRKRHLGARVYSILLGTFFLIISWVFAQTRYQLALDSPYYMVVTLLLVVLSQSFLMSDRLRSAFVQSERLSRRLLIQDRQKDEFLAKTSHELRTPLHGIVNLSQSLLDQAETPLQAEHRDNILLLNRLGRRLAGLVGDILDLNRIRYGELRVQLRPVDMRVSAEFVWETLAIASVNPGIRLLNELPAELPLVLADENRLRQILHNLLENGLKYTERGTVSLSAARQGDMLAVTVSDTGRGIPPELREELFQPFVHGRESGAGSREGIGLGLSIARQLVELQGGAMSLESEVGRGSRFTFTLPVADAGERPAGAAAAPSSAMRAEGSEARHGASAPHPMRMGEGGGSAAALHILIVDDEPSNLKVALDAVSSLGHRFTAVSSGAEALEALRRRQPDLVLLDLMMPGVSGLDVCREIRSLHGLSELPVLMLTASGQTADIVAAFAAGANDILHKPFELAELKARVQSLLAMKSSSEQAVRREMDFLQAQITPHFLYNTLNALIGLSYKDVDKLRETIEHLTTYLRAKFTFVLAEAVPLERELELARAYLAIEQLRFGPRLQVECVVDEGARALLPPLTLQPIVENAVRHGIGPKPEGGTVTVSIRSIPVGVEIRVEDDGVGMDEAMLARLEAGQAGGIGIGNVNRRLQMRYGRKLDIASRPGAGTRMTMIVTKEERA
>NZ_CP045802|1759147:1844134|1795651_1796380_+|WP_028599899.1|DBSCAN-SWA
MNAAERNDPVRVLLVDDHPHGREGMRMIVSEDPFFEIAGEASGGEEAVARAEELQPDLILMDIRMPGVGGLEATSRIKASLPSVKIVMVTVSDDIADLFEAIKRGAQGYLLKNLSPSAWLDYLRAVSLDQAPMSRELATRILQEFLPGGRASASADPRTAIPSAPRTAASTLSPLTEREKEILERVARGDSNREAAAALGISENTVKNHLKNILQKLHLDNRVQLARYAYENGLMDRGAGGG
>NZ_CP045802|1759147:1844134|1831511_1832492_+|WP_153783185.1|DBSCAN-SWA
MKLTLERKPFGDFWMNCMLNQAFSIAQSVHPSYRDAAYLNLYRYFRWEAATDREFRYPTIDSLYYLSDTEWEKFPLTGVIRRIVPMHFRDESRMLDEIRDVLRSGRNLSLNVDLFGWLPDSMAWQKFHWYHYSLFNGFDEEKGVFYVIDDTLAGYGEHEVPEERVREAFAQSEYKLDPGYAGPACYVYELQPDIVPFELRLEEVAAHADRLSQELEAFGMDGMWRVDEAPGEKREQQLTYGLVGINIIVNRQEANAGLLERLRLKKLLEDELLDELDEQLGRIREGWAALKQRFADGSFRRERDAELAERLLARERELWSRLAAEA

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_101808325.1|1759147_1760407_-|transposase	IS256 family transposase	A0A0K2CZ57	Paenibacillus_phage	2.1e-138	60.6
WP_153783160.1|1761448_1762387_+	hypothetical protein	NA	NA	NA	NA
WP_153783161.1|1762408_1763023_+	hypothetical protein	NA	NA	NA	NA
WP_153783162.1|1763019_1763211_+	hypothetical protein	NA	NA	NA	NA
WP_028599914.1|1763403_1763706_-	hypothetical protein	NA	NA	NA	NA
WP_153783163.1|1763840_1765352_+	VWA domain-containing protein	NA	NA	NA	NA
WP_153783164.1|1765528_1768582_+	response regulator	Q8QKV7	Ectocarpus_siliculosus_virus	6.4e-32	28.9
WP_153783165.1|1768578_1769688_+	response regulator	NA	NA	NA	NA
WP_153783166.1|1769862_1773102_+	hypothetical protein	NA	NA	NA	NA
WP_153783167.1|1773183_1774053_-	ATP-binding cassette domain-containing protein	NA	NA	NA	NA
WP_028599909.1|1774066_1774912_-	hypothetical protein	NA	NA	NA	NA
WP_052333479.1|1774892_1775483_-	RNA polymerase sigma factor	NA	NA	NA	NA
WP_153783168.1|1775493_1777752_-	hypothetical protein	NA	NA	NA	NA
WP_028599907.1|1777748_1778624_-	ATP-binding cassette domain-containing protein	A0A2H4PQG7	Staphylococcus_phage	1.6e-15	29.8
WP_153784697.1|1779001_1779727_+	5-oxoprolinase subunit PxpB	NA	NA	NA	NA
WP_153783169.1|1779903_1784256_+	hypothetical protein	NA	NA	NA	NA
WP_153783170.1|1784322_1784853_+	hypothetical protein	NA	NA	NA	NA
WP_101808824.1|1785050_1786343_-	beta-ketoacyl-ACP synthase II	NA	NA	NA	NA
WP_028599905.1|1786457_1787315_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_153783171.1|1788808_1789417_+	MOSC domain-containing protein	NA	NA	NA	NA
WP_153783172.1|1789438_1790206_+	5-oxoprolinase subunit PxpA	NA	NA	NA	NA
WP_028599902.1|1790676_1791063_+	gamma-glutamylcyclotransferase	NA	NA	NA	NA
WP_153783173.1|1791257_1791425_-	hypothetical protein	NA	NA	NA	NA
WP_153783174.1|1793097_1794702_+	copper resistance protein CopC	NA	NA	NA	NA
WP_028599900.1|1794765_1795632_+	two-component sensor histidine kinase	NA	NA	NA	NA
WP_028599899.1|1795651_1796380_+	response regulator transcription factor	NA	NA	NA	NA
WP_153784698.1|1796589_1797315_+	DUF1775 domain-containing protein	NA	NA	NA	NA
WP_153783175.1|1797983_1799018_+|tRNA	phenylalanine--tRNA ligase subunit alpha	A0A2K9L3A8	Tupanvirus	7.2e-28	36.9
WP_153783176.1|1799040_1801476_+|tRNA	phenylalanine--tRNA ligase subunit beta	NA	NA	NA	NA
WP_153783177.1|1801676_1804709_+	hypothetical protein	NA	NA	NA	NA
WP_153783178.1|1805188_1805572_+	aspartate 1-decarboxylase	NA	NA	NA	NA
WP_153783179.1|1805586_1816182_+	amino acid adenylation domain-containing protein	A0A2K9KZV5	Tupanvirus	6.6e-84	22.6
WP_153783180.1|1816115_1818128_+	amino acid adenylation domain-containing protein	A0A2K9KZV5	Tupanvirus	1.3e-49	29.9
WP_153783181.1|1818124_1818991_+|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_153783182.1|1818987_1819791_+|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_153783183.1|1819787_1820576_+|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_153783184.1|1820634_1831515_+	amino acid adenylation domain-containing protein	A0A2K9KZV5	Tupanvirus	3.0e-116	24.6
WP_153783185.1|1831511_1832492_+	hypothetical protein	NA	NA	NA	NA
WP_153783186.1|1832464_1833286_+	alpha/beta fold hydrolase	NA	NA	NA	NA
WP_153783187.1|1833282_1834536_+	acyltransferase domain-containing protein	NA	NA	NA	NA
WP_153783188.1|1834785_1835250_+	4'-phosphopantetheinyl transferase superfamily protein	NA	NA	NA	NA
WP_153783189.1|1835379_1835775_-	cytochrome C oxidase subunit II	NA	NA	NA	NA
WP_153783190.1|1835939_1836296_-|holin	phage holin family protein	NA	NA	NA	NA
WP_028599889.1|1836476_1838840_+	endonuclease MutS2	Q94M10	Lactobacillus_phage	1.3e-08	31.4
WP_153783191.1|1838861_1839278_+	DUF350 domain-containing protein	NA	NA	NA	NA
WP_153783192.1|1839411_1840008_+	hypothetical protein	NA	NA	NA	NA
WP_153783193.1|1840125_1841418_+	MFS transporter	NA	NA	NA	NA
WP_052333442.1|1841367_1842489_-	hypothetical protein	NA	NA	NA	NA
WP_153783194.1|1842712_1843402_+	hypothetical protein	NA	NA	NA	NA
WP_028599885.1|1843503_1843728_+	hypothetical protein	NA	NA	NA	NA
WP_028599884.1|1843756_1844134_+|coat	spore coat protein	NA	NA	NA	NA

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP045802|2346932:2356127|DBSCAN-SWA
CTTATCCAGCACAACAGGATAATTTAGATACATCTTTATTGATCGTAAGAGCTGCTAGTTTTAATCCCTCAGCCATCGTTAAATACGGTGCTAGGCTATCGCGTAGATCCTCGACCGTTAAACCGAACTTGACTGCAAGTGTCGCAGCGTAAATTACATCTCCGGCATTTTCAGCGACAATATGAACACCAAGCACCGTTAACGACTTGGAATCAGCCACTAATTTAAAAACGCCGGTTGTTTCGCGATTAACAAGTGCTCTAGGCACCGAATCCAAAGGAAGAATGGACGTTTTAACCTCATACCCTTTTGCCTTGGCTTTCTCTTCCGTGAGTCCTACAGTAGCAACGGAAGGAGAAGTGAACGTAACACCTGGAACAGCTTCAAGATTTACCTTTTTCTCTAAGCCGCCTATTGCATTATCGGCCGCGATGCGACCTTCATAAGCAGCCACATATACAAACTGCGGCCCCATCGTCACATCGCCTGCAGCATAAATTCTAGGATTCGAAGTGTTTAAAAAATCATCGACGACGATTTCGCTTTTGGAACCTATATTTACGTTCGCAGCATTAAGGTTTAGTGCTTCAATATTTGGTTTTCTACCGGTTGCAATAAGCAGCTGCTCGACTTCGATGACTTTCTTTTCGCCATCTACGGAAATATGCACTTGTTTTAGATCGCCACTTGCTTCTATGCGATCATACGTTACACCGGTAATCAAGTGAATCCCTTGCTCCGTTAAAGCCTTTGTCACCGCTTCGGAAATTTCAGGGTCATACTCTTTCAAAATGCGAGGACTTCTTTGCATCAGCGTAACATCTGACCCTAGATTGTGAAAGAGTTGACCCAATTCCATTGCAATATAGCCTGAGCCAATGACGGCAACCGTTTTAGGCAATTGTTTGAGCTCAAGTAGTGATGTGCTTGTTAAATAATCCACGTCCCTTAATCCTTGAATATCCGGAATGGACGGAGAAGCTCCTGTGGCAATTAAAAATCGTTTCGCTGTAACCAGTCGTCCACTTACCTCAATGGTTTTTTCATCTACGAATGTTGCCTCTCCTCGAATGAGTTCAAATCCGTACTCACCAATCAAATGTTCATACTTCTGTTCTCGCATACTGGCTACCAGTTCATTTTTATGTTCGACCAACTTTTCCAAATCTACTTTTCCTGTTGATGTGGCTAGTCCCAAGAATGGGTTGCTTTTGGCTAAATGATTGATTTCACCGGCACGAAGCAGCGTTTTTGATGGAACACAGCCAACATTTACGCAGGTTCCGCCAACAATTCCCCGCTCAATGATCGCGACCTTTGCGCCATATTCCACCGCTTGAATCGCTGCGGAAAAAGCTGCTCCACCGGAACCGATGATCAGAAAATCATAGTCGCCTTCATCGCCGAGAACCGGAGCATCATGAGTTTCTATCACTTCCGCATCTCCGGATTGATATTTTGCCTCGTTAATGGCTTTTTGGGCGGTTTCGATCATAACGTCATCGGGCAATTCAAACGTGGCTTCATTACGGTGAAAACTCGTCTCGATATTGGCGGCTCCAATGTTTTTAAGTGCGGTTGCTACGTGTTCTTCGCAGCCGCTGCATGTCATGCCTTGAACGTTGATTCGGTATTTTTTCATTTTTTATCCTCCCATTACATCAAACCCATATTTTGTAACCGATGATTGGATTAGCTTTACATCGGTTTTCAGATCATCAAAGGAAACCGTCACTTTTCCAGTGCTTCCCTTAGGTTCAATTTCTACTTTGCTGACTCCGTTTACCTTGAAATTAAATCTTGAATCACAGAAGGTGGGCAACATTCTAATCCCGTGACCGTGAACGTCGCCGATTGATTTGCAACAGTTGTACTTGCAGTTTGCACTGCTGCCGATGATTTTCATTGCTGCCGCCTGCCGTACCCGTGATCATTAAAAACATCTGGTACTTGATTGAAATAATCGCGAGTGTACCTGCCAAACCGGATAATCCGAGTGGAATGAGAATTAAGGGTCCGAGGCAGCAAGAAAGGCAGATAATACCGCCCCCCAGCTCGTTAGTTTTTCTCTCAAAATCATTCACCTCGTTTTTGCCCTGGTACTGAGCAGCAATCGTGTGTCACATCGGTTTTTTCTTGTATATTCGTCCTTTTGAATACCATACAAAGGGAAATCACAAATAGAATAGCCAAAATAGCACTAGCGGCGCCTTGATGGGCTGCAAAATACGCACCCAGTGTTGTGCCAGCAAGCAGAGGAAGAATCAAAACGAGATGGCAAGGGCAGGAAAGCAGAGCTAAAAAGCCCCATCCCATTTTCTTTGTATTGTCTTTCACAGGATTTCCTCCTCATTGTCAATTAACGCCTCGATGATTGGGCATTCATGAATTGCCTTTTCATCTGGACAGCGGTCTTTTAAATCTTTTAGCATACATTCGATTCGCTCAAGGTCTCTTATTTTCAACCGAACATCTTCAAGTTTTTGAACAACAAAATCGTGCATATCCGCACATCTCACATCGTCTTTATCAACGACACCAAGCAATTTATCAATTTCAGATAACGTAAAACCAAGCTCTTGTATACGTTTAATGAACATGATTCGTTTTACCGCATCTTCCGGATAAAGCCGGTAACCTGCATCCGACCTTACAGGTTCAGCAATCAGACCTTTTCGTTCATAATATCTAAGCGTTTCTTTATTCACATTACATAATTTGGATATATCTCCTGAATGATACCTCATGGTTCACCTCCCTCATAAGTGTAAACCCTGTACCATGATACATAGTCAAGACATCTTTATTTATTTCCTTAAAGTTCCGAAATAATTTTATTTTGGTTGTATTAGCTATGTGGCCGAGCAAGAGCGGAAGAAGAACCGGCAGCGGCAGGCGGAAGGAATCGAGGTTCCCCGAGAGGAGGGCTGTTGTATTCGGCCGACCCAAGCAGGAGATCGATGGAAAATGTGGAGGCGTACCGGGAATGGAAAGCAGGCCAGATTACCGCGACGGACGCTATACGTCGGATCGGTATGAAAAAGCCTACATTTTACCGGCGAGTGAAGGAATACGAGGAAATCAATGAGCCGTTCTAAGCTATCGTCAGTTCCGCGGCGGCCAATGATGGGGTAGTACCAGCAAACAAAGCTGACACCACCCGTAAAGTACATGGGGACATTTCCCCCTCAATACCTTGGCCTAGGAGATACCTAGTTAAGTTTGATGTTTACGAACTATGATTTTTCGATACATACCGTTAAATAGGGCTGATGCATCTTCTTCCACTCGAATTTGTTTCTCGTACGGCATAATGATTTGCTCAAAATGACGACCGATGTCTGTACCCATCAATGCTACGACGGGGCGAAGAATTTTCTTCATTACAGGCAACTCCCGAGATGGAGGGGCAAACTTATCGAAAATGAGAATACGTCCCCCAGTTCGCGTAACCCGAATCATTTCTTGAAAACATTGGTTCGGATCAGGGACCACAGATAAGATCAGATTCGCAATGACCATATCAAATGATTCCGGTGAAAAGGTCAAATTTTGTGCATCCATTTCCATGAAAGTAACGTTAGGAGAGTCATATTGATTCTTAGCTCGGCCAAGCATTTCGGGTGACAAGTCGATTGCAGTTACAGAAATATCTTTCCCCATAATGAACCGCAAGTCTGCACCTGTCCCGACGCCCACAAAAAGAATTTGGCTGTTAGCTTTAATGTCGACGTCCTCAAAAATCTTTTTCCGAGCCTTTAGAAAAGGCCCGGAATTAAAGAAATAATCATAAAAGGGTGCCCATACCCGATAAATCACTTTATTCCAAGGGTTATTCATAGGCGATCATTTCCCTTTCACTTTTAACAAACGTAAGCTGTTCAAAGTAACAATTAGGGTAGCTCCCATATCTGCAAAAATAGCCATCCATAGCGTAAGCCATCCAGGAACAATCAAAGCCAAAGCGACAAGTTTAATCCCGAGCGAGAACGTAATGTTTTGCTTTATTATCGCAAGGGTTTTACGGCTTAACCGAATCGTATACGGGAGTTTACCTAAGTCGTCAGCCATAAGTGCAATGTCCGCCGTTTCAAGCGCCGTATCCGTACCCGCGCCTCCCATAGCGATACCAACCGTTGAAGCCGCAAGCGCGGGCGCGTCGTTGACGCCATCGCCAATCATTGCGACATTGCCATAGTCTTTACGAAGCTGCTTAATGTAATCTAATTTATCTTGCGGCATGAGGTCGGCTTTAACGTCTGTAACATTCAACCGGCTCCCGATAGCTTCGGCGGTTGCTTGATTATCACCCGTAAGCATAATCGTTTTCTTGATGCCAATTTCGTGCAATTGCTTAATAACGTCTTTACTGGAATCGCGCACTTCATCGGCCACGGCTATTAAGGCAAGAACTTGTTGTTCCGTTCCCAAGACCATAACCGTTTTCCCTTGTTTTTGTAGAGCTTCGATACGTTGATTCGTTTCAACATTCATATCGGAGCGAAGTTCTGCAAAGAGTTTTGGACTACCGACGTAATACAATTCCTCGTTTACTTTTGCTTTAACGCCTTTTCCAGTTATCGATTGGAAATCCTCAACGGTGAGGGATAAGTCGGCTCCGAGATTTTCAGCTTTACGAACAATCGCGGAAGCGAGCGGGTGTTGCGAACCTTTTTCGATAACTGCCGCGATGGCAAGCAATTCTTTTTCGTCTTTCGTTCCGAAAGTATGGACATTTGTTACTTCCGGGAATCCTTTCGTCAGCGTACCCGTTTTATCGAATGCGATTGCGGCAAGGCGACCAGCTTCTTCAAGGTGTATGCCGCCTTTGATAAGGACGCCATTTTTCGCCGCGTTTCCGATAGCTGTAACAATCGAAACAGGTGTCGAAATGACCAATGCGCAAGGACAGCCGACGACGAGTAACGCTAATCCCCGATATACCCAATCGCCCCAATCAGCGCCGACGAACAGAGGGGGAACAACGGCAATACCTAATGCCAAAATCATAATCGCGGGCGTATAGTATTTCGCAAATCGGTCAACGAACGCTTGTGAAGGTGCACGTTCGGCTTGTGCTTCTTCAACAAGGTGAATAATTTTCGAGATTGTAGTATCCTCGACATGCTTCGTTACTTTGACCTCAAGCAATCCTTCTTCGTTTAATGTGCCTGCGAAAACTTCATCATCAATTGTTTTCGTTACGGGAACCGATTCGCCGGTTATCGCAGCTTGGTTAATGGTTGATGTCCCTTTAATAACCACGCCATCCATTGCGAGTTTTTGACCAGGCTTTACAATCATGACGTCGCCAACCTGTATATCATCGACACTTACCGTAATTTCTTCGGAACCGCGTCGAATCAGAGCTTCCTTCGGTGCAATATCCATCAGGGAACGAATGGATTGACGCGCTTTCTCCATAGAGTAACGTTCCAAAACTTCACTAATTGCAAACAAGATCACAACCGTCGCGCCTTCGCCCCATTTGCCGATCGCCGCGGCACCGATGATGGCCACCGTCATAAGGGTGTTCATATCGAACTGAAGCCGGAAGAGATTTTTAAGCCCTTTTTTGAATAGATCGTAACCGCCAATGAGAATAGAAGCCGCAAAAATGACTGCGGATAAGATACTTCCCTCACCTAGAAAATAACCTGCCGCAAGCAATACGGCAGAAACCAACACGTTCCAATGCTCTTGCCAAAATGGCTTTTTCTTTTCAATCGTCCGTTGTTTTTCAGGTGTGACTTTCAGGCTTTCAAAAGCTCCAGCCTTTTCTAAATCCTCCATTGTGGTACTTCCATAAACGGTAATCTTGGATGCTCCAAAATTGACTTGAGCATCTTTAACGCCAGGCAAACCTTTTACATTTTTCTCGAAAATGCCTGCGCAATTCGTACAGGTAAAGCCTTGAACTCTGTAGACGTTTTTATCTTCTGTGTTTTCAATTTTATTTTCCATTGGTGATCAACTCCCGCGAATGAGTAGAAGCTAGCTGTACCAATTGACGAACATGGTCGTCTTCTAGCGAATAAAAAACTAATTTGCCATCCTTGCGGTATTTGGCTAGGCCAAGCTGCTTTAAGGTGCGAAGATGGTGTGAAGCTGTTGCCAACGAAGAACCGATAATGTTAGCCACATCACAAACACATAATTCATCTTCTTCGCAAAGGGCAAAAGCGATTTTCATTCTGGTTTCGTCAGCTAAAACCTTAAACATCTTTATCATGCCTTGAATATTTTGTCCTTCAAGTGCATGTTGTACCTTTCGGACTTTAGGTTCGTCATAACAATAAATTTCACATGAGTCCTTTTCTTTCATACCGCTCATATTCTCACCTCTATAATCAAACGAGTATTTGATTGTTATCATACAACAAACTTTTCGATTATTCAAATGTATATTTGATTATCTATCAAACATATCTAAAATATTCTTTTCAACGTTGATACTGCGTTAACAATTGGCGTATATGATCATAATAGAAATAAGCAAATAATTATATGGCTATTTACAGCGGGTAGGGGAGTGTGGGAGAATGAAACGGGAAGTCAAACGAATTTATTTCCTTTGCGGGCAAAATCGGTGCCGAAGTCAGATGGCCGAAGCTTTTGCCAAGTTTTATGGCGGGGATCATGTAGTGGTGGAGAGTGCTGGATTAAATCCATCCGAAGAAGTGCATCCTTACACCATTGAAGCTATGCGTGAGGTAGGCATCGATCTTTCCCAGCATGTTTGCAAAAAAATTGATATGAAATTTTTTCTAGCGTCGAATGCGATCGTCAAGCTGTGCGAACAAATTGTGGAGCGCTGTCCTATCGTACCGTTTAAGATCATGAACGTCGAGTGGAACATCCCTGACCCGTTGGCCGTAGACGGCGGCAGCCTGGAAGACGTGAAGAGAGCGCGTGACGAGATTCGGGAGAAAGTGATTGGGTTGTTAAAAGGGATGGACATTCCCGTCGCTTAAAAGGAGTGAAGCAGTTGAGCAAACTAGAAGAAGTAGCGGATGCCTTGAAGCTATTAGGGGACCGGAACAGGCTCACTATCGTAGCCATGTTGCAGGTGAAGGAACTGTGCGTGTGCGAGATCGTGGACATTTTGAAAACAAGCCAGCCCAATATCAGTCAGCATATGCGCAAGCTGAGGGACGGGGGCTTGGTCAAAGAGTCCCGCAGGGGGCAATGGGTTTATTATTCGCTCTGCCTGGAAGACAAGCCTTATATTTTGGATATTCTAAAGGAAATTCCTTCGCAAGCGGCGATGATTGAGCCTGTCGTTTGCGAAACCAATGATTGCTGTACGTAGTTCAGGAGGACGCATATGGTTTATGTAGCGATTTTCATTTTCTTGGTAACGTTGCTTTTTGTCATCTGGCAACCGAAAGGATTAAACATCGGCTGGTCGGCAAGTGTCGGAGCGATCCTTGCTTTAATATTTGGCGTGGTCAGCTTCGCTGACGTCGGCACCGTAACCGGCATCGTGTGGAATGCCACCTTGGCGTTTGTGGCCATTATTTTAATCTCACTGGTGCTGGATGAAATCGGATTTTTTGAGTGGGCTGCCTTGCATATGGCGCGGCTGGCACGCGGAAACGGTCTACTCATGTTTGTATTTATCATCCTGCTTGGATCGGCGGTTGCCGCGCTGTTTGCCAATGACGGCGGGGCCTTGATTATTACGCCGATTGTGCTCGCCATGGTCCGGGCGCTTAAGTTTGATGAAAAGATGATCCTACCGTTTATTATGGCGAGTGGGTTCATTGCCGATACGGCATCTTTACCGCTTGTCGTCAGCAACTTGGTGAATATTGTATCCGCCGATTATTTCAACATCGGTTTTGCGGAATACGCGAGCCGCATGATTGTTCCGAATTTCTTTTCCGTCATAGCGAGCCTCATTGTGCTGTATCTGTATTTCCGGAAAAGCATCCCGAACAATTACAATCTCACGCAACTGAAAAGGCCGAAGGAAGCCATCAAGGATATGCGGCTGTTTAAGTTATCTTGGGTCATTTTAACCGCGCTGCTTGTTGCGTATTTTATTAGCGAATTTTTCTCGATCCCTGTATCCATTATTGCCGGGGTTGCAGCGATTGCCTTTTTGTTCGCGGCGAGAAAGAGCCCTGCGATTCATACTTGGAAACTGGTAAAAGGCGCTCCCTGGGCTGTCGTGATCTTCTCTATCGGCATGTATGTGGTCGTTTATGGCTTGCGCAATGCCGGACTTACGGATGCACTGGGCAGCGTCATTCAAGCGGTCGCAGACAAAGGGTTATTTGTGGCTACCGTAGGGATGGGCTTTATTGCAGCCATCCTGTCGTCCATTATGAACAACATGCCAACGGTCATGATTGATGCGTTGGCCATCCAAGGTACACAAACCGATGGATTCATTCGTGAGGCGCTGATCTATGCGAATGTGATCGGTTCGGACTTAGGGCCGAAAATTACGCCAATCGGCTCCCTGGCCACGCTGCTTTGGCTGCATGTACTATCCACAAAAAACGTGAAAATCAGATGGGGCTATTATTTTAAAGTCGGCATCTTGTTAACCATTCCCACGTTGTTCATAACGCTCACCGGTCTTTATGTATGGCTTTATGTTCTCCAGACGCTACAGGTGAATGTATGGCTATGTATTGCGGTGATTGTGGTCGTCCTGGTGGTGGTTGCAATGATCATGAAGTCTTTTATGGGAAGTAAACAAGCGAAAAGAGTTCATCAAGGCGATTAATGAATTGAAATCAAAAGGAGATTGTTCACCATGGAGAAAAAACCGTTAATTTATTTTTTGTGCACCGGAAATTCTTGCAGAAGCCAAATCGCGGACGGGTTTTTAAACGCGCTAGGCAGCGACAAATATGAAGTCAAAAGCGCAGGTCTTGAAGCACACGGACTGAATCCGCGTGCGGTGCAAGTCATGCAAGAAGCTGGGGTAGATATTAGCAAAAACACCTCCGATGTGATCGATCCGGACATTTTGAATCGCGCCGATTATGTCATTACCTTATGCGGCCACGCCGACGAGCATTGCCCTGTGATCTCCAACAAGAACGTAACGAAATGGCATTGGGGTTTTGATGATCCGGCAAAAGCAACCGGAACCGAAGAAGAAATCATGAACCAGTTCCGCACCGTTCGCGATTCGATTAAGAGCCGGATTGAACAATTCGTCAAAGAAGGGAAATGA

Protein sequences of DBSCAN-SWA_2

>NZ_CP045802|2346932:2356127|2354258_2355671_+|WP_021877420.1|DBSCAN-SWA
MVYVAIFIFLVTLLFVIWQPKGLNIGWSASVGAILALIFGVVSFADVGTVTGIVWNATLAFVAIILISLVLDEIGFFEWAALHMARLARGNGLLMFVFIILLGSAVAALFANDGGALIITPIVLAMVRALKFDEKMILPFIMASGFIADTASLPLVVSNLVNIVSADYFNIGFAEYASRMIVPNFFSVIASLIVLYLYFRKSIPNNYNLTQLKRPKEAIKDMRLFKLSWVILTALLVAYFISEFFSIPVSIIAGVAAIAFLFAARKSPAIHTWKLVKGAPWAVVIFSIGMYVVVYGLRNAGLTDALGSVIQAVADKGLFVATVGMGFIAAILSSIMNNMPTVMIDALAIQGTQTDGFIREALIYANVIGSDLGPKITPIGSLATLLWLHVLSTKNVKIRWGYYFKVGILLTIPTLFITLTGLYVWLYVLQTLQVNVWLCIAVIVVVLVVVAMIMKSFMGSKQAKRVHQGD
>NZ_CP045802|2346932:2356127|2346932_2348573_-|WP_021877410.1|DBSCAN-SWA
MKKYRINVQGMTCSGCEEHVATALKNIGAANIETSFHRNEATFELPDDVMIETAQKAINEAKYQSGDAEVIETHDAPVLGDEGDYDFLIIGSGGAAFSAAIQAVEYGAKVAIIERGIVGGTCVNVGCVPSKTLLRAGEINHLAKSNPFLGLATSTGKVDLEKLVEHKNELVASMREQKYEHLIGEYGFELIRGEATFVDEKTIEVSGRLVTAKRFLIATGASPSIPDIQGLRDVDYLTSTSLLELKQLPKTVAVIGSGYIAMELGQLFHNLGSDVTLMQRSPRILKEYDPEISEAVTKALTEQGIHLITGVTYDRIEASGDLKQVHISVDGEKKVIEVEQLLIATGRKPNIEALNLNAANVNIGSKSEIVVDDFLNTSNPRIYAAGDVTMGPQFVYVAAYEGRIAADNAIGGLEKKVNLEAVPGVTFTSPSVATVGLTEEKAKAKGYEVKTSILPLDSVPRALVNRETTGVFKLVADSKSLTVLGVHIVAENAGDVIYAATLAVKFGLTVEDLRDSLAPYLTMAEGLKLAALTINKDVSKLSCCAG
>NZ_CP045802|2346932:2356127|2349007_2349247_-|WP_083436182.1|DBSCAN-SWA
MGWGFLALLSCPCHLVLILPLLAGTTLGAYFAAHQGAASAILAILFVISLCMVFKRTNIQEKTDVTHDCCSVPGQKRGE
>NZ_CP045802|2346932:2356127|2353473_2353905_+|WP_021877418.1|DBSCAN-SWA
MKREVKRIYFLCGQNRCRSQMAEAFAKFYGGDHVVVESAGLNPSEEVHPYTIEAMREVGIDLSQHVCKKIDMKFFLASNAIVKLCEQIVERCPIVPFKIMNVEWNIPDPLAVDGGSLEDVKRARDEIREKVIGLLKGMDIPVA
>NZ_CP045802|2346932:2356127|2348576_2348837_-|WP_021877411.1|DBSCAN-SWA
MKIIGSSANCKYNCCKSIGDVHGHGIRMLPTFCDSRFNFKVNGVSKVEIEPKGSTGKVTVSFDDLKTDVKLIQSSVTKYGFDVMGG
>NZ_CP045802|2346932:2356127|2350777_2352895_-|WP_021877416.1|DBSCAN-SWA
MENKIENTEDKNVYRVQGFTCTNCAGIFEKNVKGLPGVKDAQVNFGASKITVYGSTTMEDLEKAGAFESLKVTPEKQRTIEKKKPFWQEHWNVLVSAVLLAAGYFLGEGSILSAVIFAASILIGGYDLFKKGLKNLFRLQFDMNTLMTVAIIGAAAIGKWGEGATVVILFAISEVLERYSMEKARQSIRSLMDIAPKEALIRRGSEEITVSVDDIQVGDVMIVKPGQKLAMDGVVIKGTSTINQAAITGESVPVTKTIDDEVFAGTLNEEGLLEVKVTKHVEDTTISKIIHLVEEAQAERAPSQAFVDRFAKYYTPAIMILALGIAVVPPLFVGADWGDWVYRGLALLVVGCPCALVISTPVSIVTAIGNAAKNGVLIKGGIHLEEAGRLAAIAFDKTGTLTKGFPEVTNVHTFGTKDEKELLAIAAVIEKGSQHPLASAIVRKAENLGADLSLTVEDFQSITGKGVKAKVNEELYYVGSPKLFAELRSDMNVETNQRIEALQKQGKTVMVLGTEQQVLALIAVADEVRDSSKDVIKQLHEIGIKKTIMLTGDNQATAEAIGSRLNVTDVKADLMPQDKLDYIKQLRKDYGNVAMIGDGVNDAPALAASTVGIAMGGAGTDTALETADIALMADDLGKLPYTIRLSRKTLAIIKQNITFSLGIKLVALALIVPGWLTLWMAIFADMGATLIVTLNSLRLLKVKGK
>NZ_CP045802|2346932:2356127|2349264_2349678_-|WP_021877413.1|DBSCAN-SWA
MRYHSGDISKLCNVNKETLRYYERKGLIAEPVRSDAGYRLYPEDAVKRIMFIKRIQELGFTLSEIDKLLGVVDKDDVRCADMHDFVVQKLEDVRLKIRDLERIECMLKDLKDRCPDEKAIHECPIIEALIDNEEEIL
>NZ_CP045802|2346932:2356127|2350147_2350771_-|WP_021877415.1|DBSCAN-SWA
MNNPWNKVIYRVWAPFYDYFFNSGPFLKARKKIFEDVDIKANSQILFVGVGTGADLRFIMGKDISVTAIDLSPEMLGRAKNQYDSPNVTFMEMDAQNLTFSPESFDMVIANLILSVVPDPNQCFQEMIRVTRTGGRILIFDKFAPPSRELPVMKKILRPVVALMGTDIGRHFEQIIMPYEKQIRVEEDASALFNGMYRKIIVRKHQT
>NZ_CP045802|2346932:2356127|2353919_2354243_+|WP_048744011.1|DBSCAN-SWA
MSKLEEVADALKLLGDRNRLTIVAMLQVKELCVCEIVDILKTSQPNISQHMRKLRDGGLVKESRRGQWVYYSLCLEDKPYILDILKEIPSQAAMIEPVVCETNDCCT
>NZ_CP045802|2346932:2356127|2355701_2356127_+|WP_048744013.1|DBSCAN-SWA
MEKKPLIYFLCTGNSCRSQIADGFLNALGSDKYEVKSAGLEAHGLNPRAVQVMQEAGVDISKNTSDVIDPDILNRADYVITLCGHADEHCPVISNKNVTKWHWGFDDPAKATGTEEEIMNQFRTVRDSIKSRIEQFVKEGK
>NZ_CP045802|2346932:2356127|2352884_2353256_-|WP_048744055.1|DBSCAN-SWA
MKEKDSCEIYCYDEPKVRKVQHALEGQNIQGMIKMFKVLADETRMKIAFALCEEDELCVCDVANIIGSSLATASHHLRTLKQLGLAKYRKDGKLVFYSLEDDHVRQLVQLASTHSRELITNGK

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_021877410.1|2346932_2348573_-	mercury(II) reductase	A0A2K5B2C5	Erysipelothrix_phage	1.0e-47	29.0
WP_021877411.1|2348576_2348837_-	transport protein	NA	NA	NA	NA
WP_083436182.1|2349007_2349247_-	hypothetical protein	NA	NA	NA	NA
WP_021877413.1|2349264_2349678_-	Hg(II)-responsive transcriptional regulator	NA	NA	NA	NA
WP_021877415.1|2350147_2350771_-	class I SAM-dependent methyltransferase	NA	NA	NA	NA
WP_021877416.1|2350777_2352895_-	cadmium-translocating P-type ATPase	E4ZFI9	Streptococcus_phage	2.4e-283	73.0
WP_048744055.1|2352884_2353256_-	winged helix-turn-helix transcriptional regulator	E4ZFI8	Streptococcus_phage	2.4e-34	52.9
WP_021877418.1|2353473_2353905_+	arsenate reductase ArsC	A0A2H4PQT9	Staphylococcus_phage	1.8e-17	42.3
WP_048744011.1|2353919_2354243_+	winged helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_021877420.1|2354258_2355671_+	arsenic transporter	A0A2H4PQU3	Staphylococcus_phage	6.0e-150	64.5
WP_048744013.1|2355701_2356127_+	arsenate reductase (thioredoxin)	A0A2H4PQT9	Staphylococcus_phage	1.3e-31	50.4

Sequences of DBSCAN-SWA_3

Nucleotide sequences of DBSCAN-SWA_3

>NZ_CP045802|2458245:2466755|DBSCAN-SWA
CATGGGCGGTACATGGGATACGACGAGCCTGCCGGCGCGTCCGGGACTGTACATCAATTTCGTGAACGCGGCGGCAGCTGTAATCAAGGGAGGAGCGCGCGGCACGGTGGCGCTGCCGCTGCTGAAATACGGCACGGCGGCAAAGGAGAAGTTCTACACGATCGAAAAGCCGGCCGAGGCGGTCGAGCTGTTCGGCGAGGCGGATGCGGCTCCGGTGCTGCTCGTCCTGCAAGGAGGGGCGCGCGAGGTTCTCGTGTACACGATGACGCCGCCGACGGGCGAGGGCGACGCGCTCAAGGCGTCCCGGGCGAAAAGCTTCCTCTCGATGCGCGACCAGCTGGAGGCGAGGCCGTTCAACGTCTTTGTCTATCCGGCCGAGGTGGAGGCGTCGGAGGTCGATCTGACGCTGGCGTGGATCAAAAGCAGCCGCAAGGACGGCAAGCACTTCCTCGCCGTATTCGGCGGCACGAGGGACGAGGACAAGGACCCGGCGCTCGGCAATGCCCGCAGCGTCAAGCTGAAGGACGACTACGCGGTCAATCTGATCACCGGCGCGGAGGCGGGCGGCAAGTCCTACTCCTCGGGCGAATACGCGCCGTATGTCGCCGGTCTGATCGCCGGCACCGGCATCAACAAGTCGATCACGTACGCCCAGGTGTCCGCGACCGACGCGCTGCGGCGGCTCAAGAACAGCGAGATCGCGGCCGCGCTCGAAAAAGGCTCGCTCGCGCTCGTCCATGACGGAGAGAAGGTCAAGGTCGAGCAGGGGCTCGTGACGAGCGGAGCCAAGATCCGCACGATCCGGGCGCGGCAGGCGGTCGCGACGGACATTCCAAAAACGGCGGCGGACAGCTACATCGGCAAGCTCGACAACAACGCCGACGGCCAGGCGGCGCTCATCTCCGCCGTGAAGGCGTACCTTGAGCGGCTGGAGCTGGCCAGCGTGCTGACGGACATCGAGGCCGGACTCGATCCGGAGCGCAAGTCCGAGGGCGACAACGTCTACCTGCGCATCGCCTACACGGAGATCGACAGCATGGAACGCATTTTCCTGACCATCGAGGTCTGAGGCAACCGAACCCAAGAGGAGGCATGAGATCGAATGCTGGATCCGACACGCGTCATCAACGGCGCTTACGGCTACGTGTACCATGACAGCAAGTGGCTGACGAACATCAAGTCCGCGGAAGCGAACGTGGAGATCTCCAAGGAAGAAGTGAAGCGCGCCGGAACGCGCTGGACCGCCCACAAGGTGACCGGACTGAGCGGCACCGGCACGATCAGCGGCTACAAGGTGACGTCCGAGTTCGTGGAGCTGATCGGCTCGATCGCCGACGACAAGAAGGGCAGCTTCATCACGGAGCTGATCCTCAAGCTGGAGGATCCCGAGTCGTACGGCGCTTACCGCGTCCGCTTGAAGGGCGTGACGTTCGACAAGATCCCGCTGCTGCACTACGAGGTCGGGTCGCTCGTCGAGGAGGAGCTGCCGTTCAGCTTCACCGGCTACGAGCTGCTCGACAAGCTCGCCGCGGAAGAAGCCTAGATGAATAACGGAGGTGAGACGTTCATGAGCGACAACCGCCAGACGGCCGTCCTGCACGCGCTGCTGAGCGCCGACACGAGGCCGCAGAAGGACATCCCGATGAAGAGGTTGGGCGTGGACTTCACGATCCAGGCGCTCGACGGCAAGACGATCAGCCGCATCCAGGAGCAGTGCACGCACTTCGCGGGCAAAGGCAGCAAGCGGGAGAAAATCCTCGACGAGGAGCAGTTCGGCGCCCTCGTCATCCAAAAGTCATGCGTCGTGCCGGACTGGACCGCGCGCGAGCTGACGGAAAAATACGGCACTCCGGCCGACGCGATCATGGGGCTGCTGCTGGCGGGCGAGATCGCGAGGCTTTCCTCCGAGATATTGGAGATCAGCGGCTTCGACAGCGACGAGGAAGAAGTAAAAAACTGATCCGGGCGGGCGGCGAGCCCTTCCTGCTCCATCTGATCTTCCAGCGCCACGGCATCGCGCCGGACGAGGTGTACAACAAGGAGGAGCGCTTCAAGCGCTTCATGTACGCCTCGATGATGCTGCAGCTGGAGGAAGAGGAGAAGGCGCGGAAGGCGAGCGAGCGGGCGGCCGCCCGCAGGTAGGATTCGGTCGATCGAAAGGAGGCGCGGGCGGATATGAGCACAGGAGGCGCTGCGCCCGGACCGTCCCAGAACGCCGCGCTGGAGCAGTTCTCGCGGCTGATGGATAAGATTCGCCGTCAGATGGAGCAGCTGTCCAAGTTGGACCCGTTGGGAGCGGCCGGGCGGAGCATAGCAGAGAAGCAGAAGCAGGCCAAGGATTTCCTCGAACAGATGAGAAAAGTCCGGAAGGATGCGGGCGATCAGATCAAGGCGCTCGGAAGGGAAGCCGCGGCAGGCACGGCCAAAGCCGCAAATGCCGCCGGCAATGTCGTGAGAGCCGCGGGAAGCGCATCGGCGAAGGCGGTCGGCAATGCCGCGAAGGCGGTCGGCAATGCCTCGGCGAGGGCGTCGAAAAGCATCGTCAAGGGAGGCATCCGCTTCGCGTTCAAGGAAAGGTCGATCGCTCCGCTGACCGGCATGATGAAGTCGGGGTGGGGAGGCGCGAAGGCGCTGGGAGGCAGAGCCAGGAGCTGGGCAGGCCAGAAATGGATGGACTCGACGAAGCCGGTCCGGGAAGGATGGGGCAAGGCGAAGGACGCTGTCTCGCAGGCGGCGGCTCCGGCAAGAGCGTATTTGGCCGAGCATAGCCGGCCGATGCGCGAGCGCTGGGCGGGCTACAAAAATCGCGGCGTGACGGCGGTCAAGTCGTATGCTCAAGGGCTTCGCGAGAAGGGGAGGGGCGTGTACGAGCAGCACAAGGGTTTGGTCAAGGAGCATGGAGCGGCGGCGGCAGCGATGGCCGGAGGCGCGATTGTCGCGGTCGGAACGAAATCGCTGGAGGCGGCCGAAACATTCGGCAAGGCTTCTTCGATCCTGCGGGCGTCCGCCGGAGTGCCTGGCGAGCAGATGGGGGAGCTGCTGGAGTCTTTCCGCAAGGTCGGATCGCAAGTGCCGCAAAACCTGGACGAAGTCGCCAAGGCGATGGGCACGCTGCGCGGCAGCTTGCCGCTCACGGGCGCCGGACTGGAGAAGACGTCCAAGACGCTGCTGGACGCGTCTCGGCTGACAGGAGGGGACAGCGCCGCCATGGCGGAGTCGCTGGCCGGCATCATGAACAGTTGGGACGTCAAGCTTGGCGACAGCTCAGGGACGCTCGACAGGTTTTTCGCCGCGAGCCGGGCCGGAAAGACCGATATGGCCGCCCTGATGAAGGGCGTGAGCGATTCGGCCGGCTCGTTCCAGGAGATGGAGCTCGGACTCGATGCCTCGACGGCGCTGATGGCCAAGTGGCAAAAGGCAGGCATCAATCCGATCCAGGATGTGCTGAAAAAAGTGGAAGGCGGAACGATGCAGCTGCCGGAGGGAGGCTTCGAAATCATCGCCTCGCAGATCCGGCAAGCGGAGTCGATCGCCGAAGCGGCCAAACTGGCGATCGGCGTATTCGGCCAAGAGGCCGGCATCGACCTGGCGCTGGCGCTGCGCGGCAGCACCGACGGCTTCAAAGGCATGCTCGGCTCGATGAGCGAGGCGAGCGGCAGCATCTCGGCGCAGTCGCAGCAGCTGCAAAGCTTCGGCGACGGCTGGGGCGCGCTGCAGAACCGGGTCACGATCGCGCTGGCGCCGCTCGGCGAGGCGCTGCTGCCGCTTGGCGAAGGCATCGTCACCGTCATGGAGGTGTTCGCGCGCAACGCGGATATTCTCGGCATCTCGGCGGCTGTCATGGCCGGGATTCTCATCGGCGTCTTCGCGCCGTCGCTGCTCGCTTCGGCCGCGGCCGCCTGGGCGGTGGCGGCGCCGATCCTGGCGATCCTCGCTCCCGTGCTGCTCGTCGGAGCGGCGGTCGCAGGACTGGCCTATCTGTTCAAGTATCATTTCGATGACATCAAGAAGTATTTCAACGACTTTGTCGGCGGCATTCTGGAAAAGTGGAACAAGGTCAAAGGCTTCCTCGGCCTCGGGGAGGACGCGACCGTCACGGTGGCGGCCGCCGGACCTGCCGGCGCGGCCGCCCTGCCCGGCCATTACCATGGCCTCGGCTACGTGCCGTACGACGGCATGGTCGCGCGCCTGCACAAGGGCGAGCGCGTGCTGAGCGCGCAGGAGAACCGCGAGCTGTCCGGAGGAGGAGCCGCCGGGCTGGCGGTGACGGTGACGGGCAATACGTTCCACGTCCGCCAGGAAAGCGACATCGACGGCATCGCCCGCGCGCTCGCGCGTGAAATCCGCGCCGCGGGAGGGCTGATGGGATGAGCGGCATGCAATTTTGGCTGACGCCGGACGGCGGAGGCAAGCGGCTGCGGCTGCCGGTCAATCCGGCCGTCCTGTCGGTGAAGCTGTCGCAGGGCTACCAGGACCTCTCGGTCGTGGCGCTCGGCGAGCGTACCGTATTCGGCGAAGCGGGCCTCAGCGAGTTTGCGATCTCCTCCTTTTTCCCCCGCGACTATCATCCTGGCTACTGCGAGCATATGGAGTTCGAGCCGCCCTGGAGCTGCGTCCAGCTCGTGGAGGGCTGGATGCGGGCCCGCAAGCCGGTGACGTTCGACATCACGGGCACGACGGTCGAGGGCGTGCCGACGACGATCCGCTCGTTCTCCTACGAGGAGCGGGCCGGCAGCCCCGGCGACCTCTATTATGAGCTCGCGCTCAAGCAGTACCGCCCGGTGCAGGCGGAGCCGGCCGCAGAGCAGGAGCGCAAGGACGGCTCGCCCACGCCGCCGGCGTTCTATGTCGTCGTCGCCGGCGACAGCCTGTGGAAGATCGCCCAGCGGATCTGGGGCGACGGCGACCGCTGGCGGGAGCTGCATGCGGCCAACCAGGCCGCCATCGGCAAGGATCCGAACCGGCTGAAGGTCGGGCTCAAGCTGGCGGTGCCGGCATGAGCTGGACGCTGACGCATGTGCGGCGCGGCGGCGAGGAGCTGGATCTGAGCGCGATGTGCATGTCGATCCGCTGGTCGGGCGATGTCAAGCAGGCGGCGCGCAAGCTCGTCGTCGAGCTGGTCAACACGGCCGACGGCCGCAGCCGGCTGGCTGAGATCGACAAGGGCGGCGAGCTGCGGCTCGCGGGCGAGTCGGGCGCGGAGCTTTTTCGCGGCGTCGTGTTCGCGGACTCGATCGACTCCGGCGGCCGCATGTCGGCGACGGCGTACGACGAGAACATCTACCTGACCAAAACGAAGGACTCGCGTCTGTTCCGCCGCATGACCGCGGACGGCATCATCCGCCAGCTGTGCGGCGAGTTCGGCGTGCCTGTCGGCGAGCTCGCCTCGACCGGCTTCGTCATTCCGAAGCTGATCCAGCGCGACAAGACGCTGTACGAGATGATGACGAAGGCGCTCGAGATGACGGAAGAGCAGAACGGACGCCGGTTCGAGCTTGGCTCGCGGGAAGGCCGGGTCGAGCTGCGGGAGCGCAGCGCGCAGCTCGTGCCGTGGCGCATCGAGGCGGGGCGGAATTTGCTGTCGGCGTCCTGCTCGCAGTCGATGGAGGAGATGAAGACGCAGGTGAAGGTGATGGGCCTCGACCCGCAGCGCACGGAGCAGGCCGTCGTCGTCCGCAGCGCCGAGCTCGCGGAGCGGTTCGGCGTCATGCAGCATTTCGTCAAGCCGAGCGCGGCGATGAGCCGCTCGATGATGCAGCAGCAGGCCGACGAGCTGCTGCGGCAGCTGGCGACGTTTGCCGACGAGGCCAGAATCGAGGCGCTCGGCATCGAGGAAGCGGTCTCGGGCGCGGTCGTCAAGGTCGAGGAGCGGCTGAGCGGCATCGTCGGCCGGTATGCGATCACCGCCGACGAGCATTCGTACGAGGGCGGCGCGCATCGCATGGCGCTGACGCTGACAGCGATGGAGGAAGCGGACTGAGGATGAAGACGCGCCGTACAACGGACAGGAGGGAAGCAGCATGGACAGAGCAGAAGGTTCGGGCGCGAGCCAGCTCGTGCAGCTCATGCGGAGCATCGGCTGGAACGCGGATACGACGATCGAGCTCGGCACCGTCGTCGCGGAGCCTCCCGAGCTGAAGATCCGGCTCGACCATACGGAGCTGGTGCTGGAGAAGGACGATCTCGTCGTCGCCGAGAGGCTGACGAGCCACATGCGCAAGGTAAAGGTGGACGCGGAGAAAGTCATGAGCGCAAGCGCGGGCTTGTCGCCCTCCTCGGCAACGCTGGTGACATCGGGAGGGACGCTTACGATTACGACGCAGAAATTGGAGATGCAAGCGGGCGACTTCGCGCTTTCGGACGCCGAGCTCACCTACATCGACGAGCTCAAGCCGGGCGAGCGCGTCATCGTCGCCGGCGTGCAGCAGGGCCAGCTGTACCTCGTCCTCGATCGGGCGGTGACGTACTGATGGCGCTGTCGCCGCTGAAGCCGCGAAGCTCGGCCGCATCCGCCGCGCCGCCGGCGCCGCGTCCGTCCCGGACGTACGCGCTCGACTTCGCTGGCGGACAGCTCGAGAACCGGCTGATCGACGGGGAGGAGGCGCTGCGTCAGGCGGTCGAGAAGGCGCTGCGGACGGCGCGCTTCCGCTATCTCGCCTGCGACTGGAGCTACGGCTCCGAGCTCGAGCGCCTGATCGGCGAGGACTTGACGCCGGAGCTGATGCGCAGCGAGGTTCCGCGCGTCATCCGGGAAGCGCTGCTCGCGGACGACCGGGTGCTGGACGTGGTGGATTTTGCCCTGGACAGCCAGGGAGACCGGCTGAGCGCCCGCTTCGCGGTCGTCCACAAGGACGGATTATTGCAGCAGGAGGTGACGCTGCTTGTTTGAGCAGCATACGAAGCAAGCGATTCTGGAGCGGATGCTGGCGGCCGTGCCGCCGGAGCTCGACCGCCGGCCGGGGTCGGTCGTCCACGACATGCTGTCGCCGGCGGCGATCGAGCTGGCCCAGCTCTACATTCGGCTCGGCCAGACGCTGGACTGGGGGTTCGCCGGACCGCAGCAGCCGGGTCCGTATCTCGATCTGCGCGCCGCCGAGATGGGACTGGCGCGCAAGCCCGGCACGAAAAGCTCCGGCGAGCTGCTGTTCGCCGGAGCCGCGGGCACCCGCATCCGCGAGGGAACGATCGCCTCGCTGCCGGACGGGACGGTCTCGTTCGCGACCCGCGAGGCGGCGACCATCGGGGAAGGCAAGCAGATCCTCGTCCGCGCGGTCTCCTCGGAGCCGGGCGCGGCCGGCAACGTGCAGCCGGGCTCGATCAGCCGCGTGCTGGGCGATCTGGCCGGCATCGTCGCCGTCAGCAATCCGAAGGCGTTCGCCGGCGGGGCGGATGAAGAGAGCGACGCGTCGCTGCTGCAGCGGTACTATGACCGCGTCCGCACGCCAGCCACGAGCGGCAACGCCGGCCATTACCGCCAGTGGGCGCTGGAGGTGGAAGGCATCGGCGACGTCAAGGTGTTCGAGGTGTGGCAAGGGGGCGGCACGGTCAAGCTGTCGCTGCTCGGCCCAGACGGAACGCCGGCCAAGCCGGACAAGGTCGATCTGGCGCGGGCAGCGATCGAGGCGCGCAGGCCGATCGGGGCCAAGGTGACGGTCGCTCCGGCGAAAGGAATCGAGATCGACGTCGCGGCGCAGCTGCGCTTCGTGCCGGGCGTGGAGCTCGAGCCGATCGTCGCCGAGTTCCGGCGGCGGCTGGCCGCCTATCTGGCCGGCCTCGCCTTTAAGAAGGACCGCGTGCCGTTCAACCGCATCGCCGGTATCCTGATCGGCATCGACGAGGTCGACGATTACGTCAGCCTGGCGATGAACGGCGGCAGCGCCGACATCGCGCTCGAGGCGGACATGGTGCCGGTCGCGGGAAAGGTCGAGATCGAGTATGACGTATAGCCTGGCGGAGCAGATGATGGGCATGCTGCCCAAGTATTACGAAGATGCGCTCGCCGCGATCGCGATCATCGAGCGCGAGGCGGCGGAGCTGGCGTTCGCCTCCGGCCAGCTGGACGAGGCGTTCCGCCAGTTTTTCCTCGAGACGGCGACATGGGGCTTGTCCCGCTGGGAAGAGGCCTGCGGCATCACCGCAAGCGGCAGCAAGCCGCTCGACCAGCGGCGCTCGCTGATCAAGTCGCGGCTGCGCGGAGCCGGCACGGTGACGCTCGCCGTCATCCGCAGCGTCGTCGATTCGTTCGAGAACGGCGAGATCTCGGTCGAGGAGAAGTTCGGCGACTGGAAGGTCGTCGTCACGTTCATCGGCAAGCGCGGCGTGCCGCCGAACCTGGCGGACGTGAAGTCGGCGGTGCGCGAGATTTTGCCGGCCCATCTGCTGCTGGAGTTCCAGTTCACCTATCTGCGATGGGAAGAGCTGGACGCGGCCGGACTGGACTGGAACGCGCTGGAGCGGCTCGGCTTCAGCTGGGACGCGCTTGAGGTGTGGAATCCTGTGGAAGGGAAGTGA

Protein sequences of DBSCAN-SWA_3

>NZ_CP045802|2458245:2466755|2463240_2464224_+|WP_043111536.1|DBSCAN-SWA
MSWTLTHVRRGGEELDLSAMCMSIRWSGDVKQAARKLVVELVNTADGRSRLAEIDKGGELRLAGESGAELFRGVVFADSIDSGGRMSATAYDENIYLTKTKDSRLFRRMTADGIIRQLCGEFGVPVGELASTGFVIPKLIQRDKTLYEMMTKALEMTEEQNGRRFELGSREGRVELRERSAQLVPWRIEAGRNLLSASCSQSMEEMKTQVKVMGLDPQRTEQAVVVRSAELAERFGVMQHFVKPSAAMSRSMMQQQADELLRQLATFADEARIEALGIEEAVSGAVVKVEERLSGIVGRYAITADEHSYEGGAHRMALTLTAMEEAD
>NZ_CP045802|2458245:2466755|2465125_2466190_+|WP_153783429.1|plate|DBSCAN-SWA
MFEQHTKQAILERMLAAVPPELDRRPGSVVHDMLSPAAIELAQLYIRLGQTLDWGFAGPQQPGPYLDLRAAEMGLARKPGTKSSGELLFAGAAGTRIREGTIASLPDGTVSFATREAATIGEGKQILVRAVSSEPGAAGNVQPGSISRVLGDLAGIVAVSNPKAFAGGADEESDASLLQRYYDRVRTPATSGNAGHYRQWALEVEGIGDVKVFEVWQGGGTVKLSLLGPDGTPAKPDKVDLARAAIEARRPIGAKVTVAPAKGIEIDVAAQLRFVPGVELEPIVAEFRRRLAAYLAGLAFKKDRVPFNRIAGILIGIDEVDDYVSLAMNGGSADIALEADMVPVAGKVEIEYDV
>NZ_CP045802|2458245:2466755|2462611_2463244_+|WP_028599619.1|DBSCAN-SWA
MSGMQFWLTPDGGGKRLRLPVNPAVLSVKLSQGYQDLSVVALGERTVFGEAGLSEFAISSFFPRDYHPGYCEHMEFEPPWSCVQLVEGWMRARKPVTFDITGTTVEGVPTTIRSFSYEERAGSPGDLYYELALKQYRPVQAEPAAEQERKDGSPTPPAFYVVVAGDSLWKIAQRIWGDGDRWRELHAANQAAIGKDPNRLKVGLKLAVPA
>NZ_CP045802|2458245:2466755|2464264_2464714_+|WP_153783427.1|DBSCAN-SWA
MDRAEGSGASQLVQLMRSIGWNADTTIELGTVVAEPPELKIRLDHTELVLEKDDLVVAERLTSHMRKVKVDAEKVMSASAGLSPSSATLVTSGGTLTITTQKLEMQAGDFALSDAELTYIDELKPGERVIVAGVQQGQLYLVLDRAVTY
>NZ_CP045802|2458245:2466755|2459346_2459787_+|WP_028599616.1|tail|DBSCAN-SWA
MLDPTRVINGAYGYVYHDSKWLTNIKSAEANVEISKEEVKRAGTRWTAHKVTGLSGTGTISGYKVTSEFVELIGSIADDKKGSFITELILKLEDPESYGAYRVRLKGVTFDKIPLLHYEVGSLVEEELPFSFTGYELLDKLAAEEA
>NZ_CP045802|2458245:2466755|2464713_2465133_+|WP_153783428.1|DBSCAN-SWA
MALSPLKPRSSAASAAPPAPRPSRTYALDFAGGQLENRLIDGEEALRQAVEKALRTARFRYLACDWSYGSELERLIGEDLTPELMRSEVPRVIREALLADDRVLDVVDFALDSQGDRLSARFAVVHKDGLLQQEVTLLV
>NZ_CP045802|2458245:2466755|2459787_2460204_+|WP_052333400.1|DBSCAN-SWA
MNNGGETFMSDNRQTAVLHALLSADTRPQKDIPMKRLGVDFTIQALDGKTISRIQEQCTHFAGKGSKREKILDEEQFGALVIQKSCVVPDWTARELTEKYGTPADAIMGLLLAGEIARLSSEILEISGFDSDEEEVKN
>NZ_CP045802|2458245:2466755|2458245_2459313_+|WP_043111535.1|DBSCAN-SWA
MGGTWDTTSLPARPGLYINFVNAAAAVIKGGARGTVALPLLKYGTAAKEKFYTIEKPAEAVELFGEADAAPVLLVLQGGAREVLVYTMTPPTGEGDALKASRAKSFLSMRDQLEARPFNVFVYPAEVEASEVDLTLAWIKSSRKDGKHFLAVFGGTRDEDKDPALGNARSVKLKDDYAVNLITGAEAGGKSYSSGEYAPYVAGLIAGTGINKSITYAQVSATDALRRLKNSEIAAALEKGSLALVHDGEKVKVEQGLVTSGAKIRTIRARQAVATDIPKTAADSYIGKLDNNADGQAALISAVKAYLERLELASVLTDIEAGLDPERKSEGDNVYLRIAYTEIDSMERIFLTIEV
>NZ_CP045802|2458245:2466755|2460203_2460386_+|WP_084137416.1|DBSCAN-SWA
MRAGGEPFLLHLIFQRHGIAPDEVYNKEERFKRFMYASMMLQLEEEEKARKASERAAARR
>NZ_CP045802|2458245:2466755|2466179_2466755_+|WP_153783430.1|DBSCAN-SWA
MTYSLAEQMMGMLPKYYEDALAAIAIIEREAAELAFASGQLDEAFRQFFLETATWGLSRWEEACGITASGSKPLDQRRSLIKSRLRGAGTVTLAVIRSVVDSFENGEISVEEKFGDWKVVVTFIGKRGVPPNLADVKSAVREILPAHLLLEFQFTYLRWEELDAAGLDWNALERLGFSWDALEVWNPVEGK
>NZ_CP045802|2458245:2466755|2460419_2462615_+|WP_028599618.1|DBSCAN-SWA
MSTGGAAPGPSQNAALEQFSRLMDKIRRQMEQLSKLDPLGAAGRSIAEKQKQAKDFLEQMRKVRKDAGDQIKALGREAAAGTAKAANAAGNVVRAAGSASAKAVGNAAKAVGNASARASKSIVKGGIRFAFKERSIAPLTGMMKSGWGGAKALGGRARSWAGQKWMDSTKPVREGWGKAKDAVSQAAAPARAYLAEHSRPMRERWAGYKNRGVTAVKSYAQGLREKGRGVYEQHKGLVKEHGAAAAAMAGGAIVAVGTKSLEAAETFGKASSILRASAGVPGEQMGELLESFRKVGSQVPQNLDEVAKAMGTLRGSLPLTGAGLEKTSKTLLDASRLTGGDSAAMAESLAGIMNSWDVKLGDSSGTLDRFFAASRAGKTDMAALMKGVSDSAGSFQEMELGLDASTALMAKWQKAGINPIQDVLKKVEGGTMQLPEGGFEIIASQIRQAESIAEAAKLAIGVFGQEAGIDLALALRGSTDGFKGMLGSMSEASGSISAQSQQLQSFGDGWGALQNRVTIALAPLGEALLPLGEGIVTVMEVFARNADILGISAAVMAGILIGVFAPSLLASAAAAWAVAAPILAILAPVLLVGAAVAGLAYLFKYHFDDIKKYFNDFVGGILEKWNKVKGFLGLGEDATVTVAAAGPAGAAALPGHYHGLGYVPYDGMVARLHKGERVLSAQENRELSGGGAAGLAVTVTGNTFHVRQESDIDGIARALAREIRAAGGLMG

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_043111535.1|2458245_2459313_+	hypothetical protein	A0A2H4J187	uncultured_Caudovirales_phage	3.0e-101	54.1
WP_028599616.1|2459346_2459787_+|tail	phage tail tube protein	A0A0N7ACS0	Bacillus_phage	1.5e-35	53.5
WP_052333400.1|2459787_2460204_+	hypothetical protein	J9QDX1	Clostridium_phage	2.2e-12	30.8
WP_084137416.1|2460203_2460386_+	hypothetical protein	NA	NA	NA	NA
WP_028599618.1|2460419_2462615_+	hypothetical protein	A0A2H4IZQ5	uncultured_Caudovirales_phage	5.0e-10	43.0
WP_028599619.1|2462611_2463244_+	LysM peptidoglycan-binding domain-containing protein	A0A2H4J2N2	uncultured_Caudovirales_phage	3.4e-36	38.4
WP_043111536.1|2463240_2464224_+	hypothetical protein	A0A2H4IZP4	uncultured_Caudovirales_phage	1.6e-37	32.7
WP_153783427.1|2464264_2464714_+	DUF2577 domain-containing protein	NA	NA	NA	NA
WP_153783428.1|2464713_2465133_+	DUF2634 domain-containing protein	S5M612	Brevibacillus_phage	1.8e-14	44.0
WP_153783429.1|2465125_2466190_+|plate	baseplate J protein	S6AVU3	Thermus_phage	1.4e-50	37.8
WP_153783430.1|2466179_2466755_+	DUF2313 domain-containing protein	A0A0A7RUW8	Clostridium_phage	1.5e-19	38.5

Sequences of DBSCAN-SWA_4

Nucleotide sequences of DBSCAN-SWA_4

>NZ_CP045802|2561313:2569960|DBSCAN-SWA
AGTGGCAAAACAAGCGAAAATCACGCTCGAAAACGGCGGCGAGGTCGTTCTGGACCTGTTCGACAAGGACGCTCCGAATACGGTCGCGAACTTTGAAAAGCTGGCGAACGAAGGCTTCTATAACGGACTTACGTTCCATCGCGTCATCCCGGGCTTCGTCGCTCAGGGCGGCTGCCCGAACGGCACCGGCACCGGCGGTCCCGGCTATACGATCGACTGCGAGATCAACCCGAACAAGCATGAGCGCGGCTCGCTCGCGATGGCTCATGCCGGACGCAATACCGGCGGCAGCCAGTTCTACATCTGCTACCAGCCGCAGCCGCATCTGGACGGCCAGCACACCGTCTTCGGCAAGATTTCCAAAGGCATGGAATACATCGACGCGTTCAAAGGCCGCGACAAGATGGCCAAAGTCGAAGTCGTCGAAGTCTGACTTCCTCGCGCGGAAGGCTCTCGTCCGAGAGCCTTTTTGTCGTTTAATCCCGACTCGTCCGCTTGCTTTTTAGCGTGCAGGCAAGTAAGATGAGTCATGCAAGCAATTGAATTCAAGCGAACCTTCGGGGCTGGGTGAAATTCCCGGGCCGGCGGTGATCCGTACCTGGCGCGTCTTCGGCATATGCCGCGGCTCGCCGGGGACGGTCAGTCCGTGACCCGCATGACCGCTTCTGCGCTTCCCTCGACCGAGGGCGCGTCGAGCGCATGCGGCTGACCTGGTGAAACTCCGGGACCGACAGTATAGTCTGGATGGGAGAAGGCTCGCTGCAAGACAGGCATGCATGAAGGCAGCTCCTCCATCATTGGAGGAGTCTGTTCAAGTCCGCCGCCCAGACATCGAGATCGGTTCCGCGCTGCCGCCCGGAGTCTGTCTTCCGATTCGATCCGGGACGGCGGTCTGTTCCCGCATTTCCAGGACGGCTTTTTTGGCTATCCGGTCGATCGGGCTCCTGCTCCTGCCGCGCGGCGACGTTTCCGACATTCCATCACCCCCGAAGGGCGCTCCAGGCGTCAATCGGGGGTGTTTTTGCATTGCGGGAAACGATCGATGATCGATATTACATGGAGCTCGCGCTCGGCATGGCGGCCAAAACGGCCGGCCAGACCGGCATCAATCCGGCCGTCGGCTGCGTCATCGTCAAGGATGGCCGCATCGTCGGCCTCGGCGCCCATCTCAAGCGGGGCGAAGGGCATGCCGAGCCGCACGCGCTGGCGATGGCGGGAGACGAAGCCCGGGGAGCGACGGCCTACGTCACGCTGGAGCCGTGCAGCCATTATGGCCGTACGCCGCCCTGCAGCGATCGGCTGATCGCGGCCGGAATCGCCCGCGTCGTCGTCGCGGAGCTCGACCCGAATCCGCTCGTCGCGGGCAGTGGCATGGCCAAGCTGCAGGCGGCGGGAATCGAGACGAAAACGGGCGTCATGGAAGCGGAGGCCAGGCGGCGGAGCGAGCCGTTCCGCAAGTTCATCACGACCCGGCTGCCCTATGTCACGCTCAAGACAGCCTCCACGCTGGACGGCCGCATCGCCGCGGCGAGCGGGGACAGCCGCTGGGTGACGGGGCCGGAGGCGCGCGAGGCCGTGCATGCGATGCGGCATCGCCATATGGGCATCCTCGTCGGCATCGGCACGGTGCTGGCGGACGACCCGAGCTTGACGACGCGGCTGTCCGTGCCGGGCCTGCATCCGGCGAGAATTGTCGCCGACTCGAGCTTGCGGCTGCCGCTGGACGCGAAGCTCGTGCAGGACGGAGCCGCGCCGACGATCGTCCTGACGTCGGAAGCCGCAGACGAAGGCCGAGCGGCCGCGCTGAGGGCGGCCGGCGTCGAGGTCATCCGCTGCGGCAGCGGCAGCTCGGTCGATCTGCGCGAGGCGATGAGACGGCTCGGCGAGCTGGAGCTCGGCTCGATCCTGCTCGAGGGCGGCGGAAGGCTGAACGGCTCGATGCTGGAGGCGGGGCTGGTCGATCGGATCTGCCTGTTCCTCGCGCCCAAGATCATCGGCGGCGAGGACGCGCCGTCGTCGTTCCGGTTCGCCGGCTTCGAGCGGATGGCCGACGCGATCGAGCTGGACGACGTCGAGGTGGAGCGCTATGGACGCGATATATGCATCAGCGGCAAGCCAGCCGCCAAGGGAGGGATCGGCTGACATGTTCACCGGATTGATCGAAGAGATCGGAGAGCTGCGCGGCGCGGCGCGAAAAGGAGAGGCGATGGTGCTCCGCATCGGCGCCGCCAAAGTGCTGGAGGGCGTCCGGCTCGGGGACAGCATCGCCGTCAACGGCGTCTGTCTGACCGTGACTGGATGCGGGCCCGACAGCTTCGAGGCCGACGTCATGCCGGAGACGTACCGGCATACGAATCTGGGCGGGCTGCCGGCGGGCAGCCCGCTCAACCTGGAGCGGGCGATGCGCGCGGACGGCCGCTTCGGCGGGCATATCGTCCAGGGCCATGTGGACGGCATCGGGCGGATCGTCGAGCGCAGGGCGTACGCCAACGCGGTGCTGTTCACGATCCGGCCCGCGGACGAAGGGCTGCGCCGCTACATCATTCCGCGCGGTTCAATTGCCGTGGACGGCATCAGCCTGACTGTGACGGAGGCGGGCGAGGACGCCTTTTCGGTGTCGATCATCCCGCATACGCTCGCCGAAACCGTGCTGCAGAGCAAGCAGGCGGGAGCGACCGTCAATCTGGAATGCGACGTGCTCGGCAAATATGTCGACCATCTGCTGCGGTTCGGCGGCAGAGGGGACGCCGCAGCCGCCGGCAGGCCGGGAGGCGCGGCCGGCGGCCCGCTGACGGCCGCTTTCCTGGCGGAGAACGGATTCGCATGAGCCAAGGCAACGAAGGAGGAGCAAGCATGGAACGATTACACCATCAAGACGGGGCGGCGCCATTCGATGCGATCGAGGATGCGGTGCAGGATCTGCTGGCCGGCAAGCCGGTCATCGTCGTCGACGACGAGGATCGCGAGAACGAGGGCGATCTGATCGCGCTCGCCGATACGATCTCGCCGGCCGTCATCAACTTCATGATTACCGAGGCGCGCGGGCTCGTCTGCGTGCCGATCGAGGCGGAGCGGGCGCGAGAGCTCGACCTGCCGCCGATGGTCGTCCGCAATACGGACTACCACGGCACCGCGTTCACCGTCTCCGTCGACCATGTGAGCACGACGACCGGCATCTCCGCACATGAGCGCGCCGAGACGGTGCGGGCGCTCGTCGACGGCGCGGCCCGCGCGGACGATTTCCGCCGCCCGGGCCATATATTCCCGCTGATCGCCAAGGACGGCGGCGTGCTGCGGCGCGCCGGCCATACGGAAGCGGCGATCGATCTGGCCAAGCTGTGCGGCGCCAAGCCCGGCGCGGTCATCTGCGAGATCATCCGCGAGGACGGCACGATGGCGCGGCTGCCGGACCTGGCGGACTTCAAGCGCAAGCATGATCTCAAGCTGATTACGATCCAGTCGCTGATCGAGCATCGGCGCCGCCGCGAGCAGCTGGTGCAGCGGGTCGTCGAGGTAAACATGCCGACCGACTTCGGCGTCTTCCGCGCGGTCGCCTACACGAACGAGGTGGACGACAAGGAGCATGTCGCGTTCGTCAAAGGACAGATCGATCCGGAGCAGCCGACGCTCGTGCGGGTGCATTCCGAATGCCTTACCGGCGACGTGTTCCACTCCCGCCGCTGCGACTGCGGTCCGCAGCTGGCGGCGGCGCTGCGCCAGATCGAGGAGGCGGGCAGCGGCGTGCTGCTCTACATGCGTCAGGAAGGGCGCGGCATCGGCCTCATCAACAAGCTCAAAGCCTATCAGCTTCAGGAGCAGGGGCTCGACACGGTCGAGGCGAACCTGAAGCTCGGCTTCGGGCCCGACCTGCGGGAGTACGGCATCGGCGCGCAGATCCTGCGCGATCTCGGCGTCCGCCGGATGCGGCTCATGACGAACAATCCGCGCAAGATCCGCGGCCTCGAGGGGTACGGACTGAGCGTGGCCGAGCGGGTGCCGATCCAGATGGAGCGCAACGAGAGCAACACGAATTACTTGAACACGAAAAAAACGAAGCTTGGCCATCTGTTGGAGTTTGAAATTTAAGCCGAATAAATTAGAATAGAAGGATGGGTTTGAAAACATGACGAAATATTACGAAGGACATCTGGTATCGCAAGGGCTGAAATACGGCGTCGTCGTCGGCCGCTTCAACGAATTCATCACCGGCAAGCTGCTGAGCGGCGCGCTCGACGCGTTCAAGCGCCATGGCGCGGGCGAGGACGAGGTGGAGGTCGCGTGGGTGCCGGGAGCGTTCGAGATTCCGCTGATCGCGCAAAAGATGGCGGAGAGCGGCAAGTACGATGCCGTCATCACCCTCGGCGCCGTCATCCGGGGCTCCACCCCGCATTTCGACTATGTATGCAGCGAGGTCGCCAAGGGCGTCGCCGCGATCAATCTGAAAACCGGCGTGCCGACGATCTTCGGCGTGCTGACGACGGATTCGATCGAGCAGGCGGTGGAGCGCGCGGGGACGAAGGCCGGCAACAAAGGCTGGGAAGCCGCTGCCGCCGCGATCGAGATGGCGAATCTGACGCGGGCGATTCAAGGCTGAGCCTGGCCTGAGGCGAGACAGCGGCCTTTAGCTTCGCGATACCGGCGGACAGGAAGAGGTGGAGCGGCATGAGCCTATTGTACAAACTGGAAGCATTCGAAGGGCCGCTGGATCTGCTGCTTCACTTGCTGGACAGGGAAGAGATCGACATCTACGACATTCCGATCAGCCGGATCGCGGATCAGTACATGGACTACCTGCATGCGATGCAGGAGTTCGAGCTGGACGTGACGAGCGAGTTCCTCGTGATGGCCGCGACGCTGCTGGCGATCAAGAGCGGGCAGCTGCTGCCCCGCCCTCCCGTCATGGACGAGTACGAGGACGCCTGGGACGACGAAGGCATGCTCGATCCCCGCGACGAGCTCGTGCAGAAGCTGGTGGAATACCGCCGCTACAAGCAGATCGCCGAGCATCTGCGCGACCGCGAGATGGCGCGCAGCCTCGTCTACAGCAAGGAGCCCGAGGACCTGACGACGTACATGAAGGAGGACGACACCCATCCGCTGGAAGGGCTCGACCTCGGCGACATCATGGCGGCGTTCCGGCGGGCGCTCCGCAAGGCGGCCAGGCGGACGCATGTCGCCCGCATCCATCGGGACGAGATATCCGTCAAGGACCGCATCCGCGACATCTCGGAGCTGCTGCGCGAGCATGAGACCGCGCTGTTCTCCCGGCTCGTAGGCGAAGCGGTGGAGCGCCACGAGATCGTCGTGACGTTCCTCGCGATCCTCGAGCTGATGAAGATGAAGCAGGTCCGCGTCTTCCAGAACAGTCTGTTCGATGATATCGTCATCCATTGGAGAGGGGAAGCGTCGGATCGTGATGGTTCAGCAGCTGAAATCGATTATTGAGGGATTATTGTTCATGGCTGGCGACGAGGGCTTGACGATCCGGCAGATCGCCGAGATCGTGGAGATCGACCAGCGCCTGTCGGAGGATCTCGTGCGCGAGCTCAAGGCCGATCTGGAGCAGGCCGGGCGCGGCATCCGCATCGCCGAGGTCGCCGGAGCGTTCCGTTTCACGACCCATCCGGAGCATGCGCCTTATTTCGAGCGGATGGCCTACTCGCCGTCCCGTTCGACACTGTCGCAGGCGGCGCTGGAGACGCTGGCGATCATCGCCTACCGCCAGCCGATCACGAGGGTCGAGATCGAGGAGATCCGCGGGGTCAAAAGCGAGAAAGCGATCCAGACGCTCGTCGCGAAGGATCTGATCGAGGAAAAAGGGCGCGCCGAGCAGATCGGACGTCCGATCCTGTACGGCACGACCCGCTCCTTCCTCGACCATTTCGAGCTGGGCTCGCTCGAAGCGCTGCCGGAGCCGGCGGCGATGACGCCCGAGGCGGAGCTCGAGGAGCAGACGCAGCTGCTGTTCGGCCGCCTGGACGGCCGCCAAGGCTCATCTTCCGAGCCCTAAGCGACATCTACGAAAAAGATCGGCTGCGGGCCGGTCTTTTTTGTCATTTCTGGGCATGCTATCCGGGAAAAGGCAGCGGTCCGGCCATCGGCGCGCGCTCTTGCTGCCGAATGACGGAAAGGGGGTCGAATCCGAATGGGAGCATGGTTCGGCTGGCTGGCGGTCGTCCTCGTGCCGCTGCTGCTCGCCGCCGCGATCGCGGCCGTTCCGGTCCGCGCCCGCGCGGAGCTGTCGCGGCATGAAGGCGACGACAATCTGTCCCTTCAGGTGAAGACGCTGTTCGGCTTGCTGAAGTTCAAGTGGGAAATTCCGATGATGAAGCTCGGCAAAAATGGGCTGCAGGTGGAGGAGCTCGCGCAGGCCGACAGTCCATCGCTGCTGCATGCCGAATCGGCGGACAAGAAGGATATCGGCGCCTCGCGCATCGCCGAGCTGCTGCAGGATGCCTGGAAGCTGCTGCGGCGGACGGAAAACCTGACCGGCCTGGTGCGGCGCACGCTGAACAAGGTGGAGATCAGCCGCTGGACGTGGCGGACGACGATCGGCACCGGAGACGCGGTCTGGACGGCGATGTCGACCGGCGCGGTCTGGTCGCTGCAGACGGCCGCGCTCGGCCTGCTGTCGCAGCTGTGCCGGCTGACCGCCAAGCCGCAGATGGACGTTCAGCCCGACTACCGCTCGGCACGGCTGGAGACGAGCTTCGACTGCATAGCGGAAATCCGCTTGGGCAATGCTATCCTTGCCGGACTGCAGCTGCTGGTCCGGATGATGAGAACGGAAGGAGGCGTCAGACTGTGGCAGAACATCCTATTCAAGGCCTGATGCAAACCGCCATGGAGAATATCAAGGAAATGGTGGATGTCAACACGATCGTCGGTGACCCCGTGCAGACGCCGGACGGAAGTGTCATTATGCCGATCAGCAAAGTCGGCTTTGGATTCGTGGCCGGCGGCAGCGACATCCGCATGGACGGCGGGGCGCGCAGCAGCTCGACCCATGCCGACGGGCATAACGCGCAGGTCGCGCTGCCGTTCGGGGGCGGCAGCGGCGGCGGCGTATCGATCACGCCAATCGCGTTCCTCGTCGTCGGCACGCAAGGCGTGCGCGTCGTTCCGCTCGACAACCAGACGCATTTGGTCGAGCGCGTCATCGACGCGGTGCCGGGAGCCTTCGAGAAGATCCAGGGCATGTTCCGTCATCACGACGGAGTCGAGCGCGTCGAGAGCACTCTTATCACGAGCGATCCGATTCTTTAGCGCCGCGGACTCGTCCCGGCTGCTGCAAGCGGCTGTCCTCCCCGGAGGACAGCTTTTTTGCGGTTTCCGGCCGGACAGGACCGGCTTGTTCATATCGGCCGGACAAGATACATACAATGGCAGCAGGAGACGGGAGCCGCCAGCGGCTTTCGCATGCCAGGAGGAGGAAGGATACCGTGGCTATTGCAGGTGCGTGGAAACGAACGGCCGCCGCCGCCGCAGGTCTCGCGCTGCTCGGCGCGAGCCTGCTCTCGGCGCCGGCGGCAAAGGCGGCGGACGCTCCCCGTCCGCCGACGACGAGCGCGCGCGCGGCCGCGCTGATCGACGTCGAGTCGGGCCGGCTGCTGTACAGCAGCGAAGCGGCCGACGAGCCGATGCGGATCGCCAGCCTGACCAAGATCATGACGGCCATTACGGCGATCGAGGAAGGCGACCTGGACAGCACGGTCACGGTCGGTCTGCGAGCCGTCGGCAAGGAAGGCTCGTCGATCTATTTGAAGCTGGGCGAGAAGATGAAGCTGAAGGACATGCTGTACGGCCTCATGCTGCGCTCCGGCAACGATGCCGCGACGGCGATCGCGGAGCATGTCGGCGGCTCGGAGGAAGGCTTCGTGAAGATGATGAACGAGAAGGCGGCCTGGATCGGGCTCGAGCGGTCCACGTTCATGAACCCGCACGGGCTGGATCAGGAGGGCCATCTGTCGACGGCGAACGATCTGGCGAAGCTGACCGCCTATGCGCTGAAAAATCCCGTGTTCGCGGAAATCGTCGGCACGAAGGTGCACAAGGCGCCGAATCCGTTCGACAGCTGGGACTACAGCTGGGCGAACAAAAACAAGATGCTCGCCTTGTACGACGGCGCCGACGGCGTCAAGACGGGCTACACGAAGACGGCGCTGCGCTGCCTCGTCAGCTCGGCGACGAGGGACGGCCAGCAGCTGGCCGCCGTGACGCTGAACGACCGGGACGACTGGCATGACCATGCGTCGATGCTGGACTGGGGCTTCGAGCATTACGAGCTGAAGACGCTGGCGTCGAAAGGCGAGCCGCTCAAGGGATACTCGCTGGCGTCGGGCCGCCAGCTGCGCTATCCGCTGGCGGAGGGCGAGGAGGCCGGCCTGTCCAACCGCCTCGTGCTGCTCAGCCGCGAGAAGGACGCGCTCGCCTATGCGCTCGGTGAGCGGGGAAGGCTCGAGTGGACGCTGGACGGACGCGCGATCGGAGCGGTGCCCGTCTACGACGCCGGCAGCCCGCGGATCGGCCAGCCGGACCGCGCGACGGCATCGTTCCGGCCTGGAGGGATGTTCTCCAGCCGTCCCGCCAGCCTCGGCGCGGCGCTGTCGAGGAGCCTGAAGGCGCTGTTCGCGACGGGAGGGGAGTGA

Protein sequences of DBSCAN-SWA_4

>NZ_CP045802|2561313:2569960|2562368_2563454_+|WP_101809018.1|DBSCAN-SWA
MELALGMAAKTAGQTGINPAVGCVIVKDGRIVGLGAHLKRGEGHAEPHALAMAGDEARGATAYVTLEPCSHYGRTPPCSDRLIAAGIARVVVAELDPNPLVAGSGMAKLQAAGIETKTGVMEAEARRRSEPFRKFITTRLPYVTLKTASTLDGRIAAASGDSRWVTGPEAREAVHAMRHRHMGILVGIGTVLADDPSLTTRLSVPGLHPARIVADSSLRLPLDAKLVQDGAAPTIVLTSEAADEGRAAALRAAGVEVIRCGSGSSVDLREAMRRLGELELGSILLEGGGRLNGSMLEAGLVDRICLFLAPKIIGGEDAPSSFRFAGFERMADAIELDDVEVERYGRDICISGKPAAKGGIG
>NZ_CP045802|2561313:2569960|2563455_2564139_+|WP_101809019.1|DBSCAN-SWA
MFTGLIEEIGELRGAARKGEAMVLRIGAAKVLEGVRLGDSIAVNGVCLTVTGCGPDSFEADVMPETYRHTNLGGLPAGSPLNLERAMRADGRFGGHIVQGHVDGIGRIVERRAYANAVLFTIRPADEGLRRYIIPRGSIAVDGISLTVTEAGEDAFSVSIIPHTLAETVLQSKQAGATVNLECDVLGKYVDHLLRFGGRGDAAAAGRPGGAAGGPLTAAFLAENGFA
>NZ_CP045802|2561313:2569960|2567457_2568144_+|WP_101809022.1|DBSCAN-SWA
MGAWFGWLAVVLVPLLLAAAIAAVPVRARAELSRHEGDDNLSLQVKTLFGLLKFKWEIPMMKLGKNGLQVEELAQADSPSLLHAESADKKDIGASRIAELLQDAWKLLRRTENLTGLVRRTLNKVEISRWTWRTTIGTGDAVWTAMSTGAVWSLQTAALGLLSQLCRLTAKPQMDVQPDYRSARLETSFDCIAEIRLGNAILAGLQLLVRMMRTEGGVRLWQNILFKA
>NZ_CP045802|2561313:2569960|2568694_2569960_+|WP_153783464.1|DBSCAN-SWA
MAAGDGSRQRLSHARRRKDTVAIAGAWKRTAAAAAGLALLGASLLSAPAAKAADAPRPPTTSARAAALIDVESGRLLYSSEAADEPMRIASLTKIMTAITAIEEGDLDSTVTVGLRAVGKEGSSIYLKLGEKMKLKDMLYGLMLRSGNDAATAIAEHVGGSEEGFVKMMNEKAAWIGLERSTFMNPHGLDQEGHLSTANDLAKLTAYALKNPVFAEIVGTKVHKAPNPFDSWDYSWANKNKMLALYDGADGVKTGYTKTALRCLVSSATRDGQQLAAVTLNDRDDWHDHASMLDWGFEHYELKTLASKGEPLKGYSLASGRQLRYPLAEGEEAGLSNRLVLLSREKDALAYALGERGRLEWTLDGRAIGAVPVYDAGSPRIGQPDRATASFRPGGMFSSRPASLGAALSRSLKALFATGGE
>NZ_CP045802|2561313:2569960|2564135_2565398_+|WP_101809020.1|DBSCAN-SWA
MSQGNEGGASMERLHHQDGAAPFDAIEDAVQDLLAGKPVIVVDDEDRENEGDLIALADTISPAVINFMITEARGLVCVPIEAERARELDLPPMVVRNTDYHGTAFTVSVDHVSTTTGISAHERAETVRALVDGAARADDFRRPGHIFPLIAKDGGVLRRAGHTEAAIDLAKLCGAKPGAVICEIIREDGTMARLPDLADFKRKHDLKLITIQSLIEHRRRREQLVQRVVEVNMPTDFGVFRAVAYTNEVDDKEHVAFVKGQIDPEQPTLVRVHSECLTGDVFHSRRCDCGPQLAAALRQIEEAGSGVLLYMRQEGRGIGLINKLKAYQLQEQGLDTVEANLKLGFGPDLREYGIGAQILRDLGVRRMRLMTNNPRKIRGLEGYGLSVAERVPIQMERNESNTNYLNTKKTKLGHLLEFEI
>NZ_CP045802|2561313:2569960|2561313_2561745_+|WP_028599823.1|DBSCAN-SWA
MAKQAKITLENGGEVVLDLFDKDAPNTVANFEKLANEGFYNGLTFHRVIPGFVAQGGCPNGTGTGGPGYTIDCEINPNKHERGSLAMAHAGRNTGGSQFYICYQPQPHLDGQHTVFGKISKGMEYIDAFKGRDKMAKVEVVEV
>NZ_CP045802|2561313:2569960|2566725_2567322_+|WP_101809021.1|DBSCAN-SWA
MMVQQLKSIIEGLLFMAGDEGLTIRQIAEIVEIDQRLSEDLVRELKADLEQAGRGIRIAEVAGAFRFTTHPEHAPYFERMAYSPSRSTLSQAALETLAIIAYRQPITRVEIEEIRGVKSEKAIQTLVAKDLIEEKGRAEQIGRPILYGTTRSFLDHFELGSLEALPEPAAMTPEAELEEQTQLLFGRLDGRQGSSSEP
>NZ_CP045802|2561313:2569960|2565435_2565906_+|WP_028599819.1|DBSCAN-SWA
MTKYYEGHLVSQGLKYGVVVGRFNEFITGKLLSGALDAFKRHGAGEDEVEVAWVPGAFEIPLIAQKMAESGKYDAVITLGAVIRGSTPHFDYVCSEVAKGVAAINLKTGVPTIFGVLTTDSIEQAVERAGTKAGNKGWEAAAAAIEMANLTRAIQG
>NZ_CP045802|2561313:2569960|2568116_2568578_+|WP_028599815.1|DBSCAN-SWA
MAEHPIQGLMQTAMENIKEMVDVNTIVGDPVQTPDGSVIMPISKVGFGFVAGGSDIRMDGGARSSSTHADGHNAQVALPFGGGSGGGVSITPIAFLVVGTQGVRVVPLDNQTHLVERVIDAVPGAFEKIQGMFRHHDGVERVESTLITSDPIL
>NZ_CP045802|2561313:2569960|2565974_2566757_+|WP_028599818.1|DBSCAN-SWA
MSLLYKLEAFEGPLDLLLHLLDREEIDIYDIPISRIADQYMDYLHAMQEFELDVTSEFLVMAATLLAIKSGQLLPRPPVMDEYEDAWDDEGMLDPRDELVQKLVEYRRYKQIAEHLRDREMARSLVYSKEPEDLTTYMKEDDTHPLEGLDLGDIMAAFRRALRKAARRTHVARIHRDEISVKDRIRDISELLREHETALFSRLVGEAVERHEIVVTFLAILELMKMKQVRVFQNSLFDDIVIHWRGEASDRDGSAAEIDY

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_028599823.1|2561313_2561745_+	peptidylprolyl isomerase	A0A1B1IVS0	uncultured_Mediterranean_phage	2.5e-22	45.5
WP_101809018.1|2562368_2563454_+	bifunctional diaminohydroxyphosphoribosylaminopyrimidine deaminase/5-amino-6-(5-phosphoribosylamino)uracil reductase RibD	A0A2H4PQS8	Staphylococcus_phage	1.5e-52	35.3
WP_101809019.1|2563455_2564139_+	riboflavin synthase	A0A2H4PQS5	Staphylococcus_phage	3.7e-36	41.8
WP_101809020.1|2564135_2565398_+	bifunctional 3,4-dihydroxy-2-butanone-4-phosphate synthase/GTP cyclohydrolase II	A0A2H4PQS2	Staphylococcus_phage	2.7e-117	53.8
WP_028599819.1|2565435_2565906_+	6,7-dimethyl-8-ribityllumazine synthase	A0A2H4PQS3	Staphylococcus_phage	4.7e-43	57.0
WP_028599818.1|2565974_2566757_+	segregation and condensation protein A	A0A1B1IVW1	uncultured_Mediterranean_phage	2.6e-06	28.1
WP_101809021.1|2566725_2567322_+	SMC-Scp complex subunit ScpB	A0A1B1IVT7	uncultured_Mediterranean_phage	2.6e-14	34.5
WP_101809022.1|2567457_2568144_+	DUF2953 domain-containing protein	NA	NA	NA	NA
WP_028599815.1|2568116_2568578_+	sporulation protein YtfJ	NA	NA	NA	NA
WP_153783464.1|2568694_2569960_+	D-alanyl-D-alanine carboxypeptidase	A0A1P8VVG5	Erythrobacter_phage	7.8e-08	34.9

Sequences of DBSCAN-SWA_5

Nucleotide sequences of DBSCAN-SWA_5

>NZ_CP045802|2820933:2831696|DBSCAN-SWA
CATGCCGGAATATCCCGAGATGGATCGATACCGCGTGCTGCTGTCGGACGCCTTGGCGGGGCAGAAGATCGTCTCCGCCGAGGTCGGCCGCGAAAAATCGCTGAATGTTCCCGCCGATGAGTTCATCCGCCGCGTGCAAGGACGCGCGGTCTGGTTCGTCGAGCGCCGGGGCAAGCATCTGCTGCTGCATCTGGACAGCGGCGAGCGCCTGCTCGCGCATCTGATGCTGGGCGGCTGGATGTTCTACGGCTCGGAGGAGGAAAAGCCGGACCGGACGGTGCAGGTGCGGCTCGGCTTCGAGCGCGGGAATCTGTACTTCATCGGGCTGCGGCTCGGCTATCTGCATCTGCTGAGCGCGCGCGAGGCGGAGGCGAGGCTCGCCGAGCTCGGTCCGGAGCCGCTCGATCCGAAGCTGACGGAGGAGCGGTTCGCGCAGCGGCTGCTCGCCAAAAAGCGAAGCGCGCTCAAGTCGGCGCTCGTCGACCAGAGCGTGCTGGCCGGCATCGGCAACTGCTACGCCGACGAGATCGCCTGGCAGGCGGAAGTGCGGCCGGGCGCGCGCATCGGCTCGCTGGAGCCGGCGACGCTGTCGAGGCTCTACGCGTCGACGCAGGCCGTGCTGACCGAGGCCAAGACGCTCGGCGGCTACATGGAGCATCCGTTCCGCGTCGGCGACGAGACGACGGGCGGCTACAACAGCCAGTGCAAGGTGTACGACCGGCCGGGCGAGCCTTGCCTGCGCTGCGGCACCAAGATCGTGCAGGAGGAGCAGTCGTCGCGCAAGGTGTTCTTCTGTCCGAGCTGCCAGAAGGAGCATTGACGATGAGCCGCTTCGGCAGGCTTGGCTGCCATGTGAGCACGCGCGGCGGCTACCGTGCGGCGGCCGAACGGGCCGCGGCGATCGGCTGCGGCTCGTTCCAGTATTTCCCCAAAAATCCGCGCTCGCTCGGCGTCAAGGCGTTCGATCGCGGCGATGCAGGCCGCTGCCGCGAGTTTTGCGTCGAGCGGGGCATCGAGTCGATCGCCCATTCGCCGTATCCGTGTAATTTGGCTTCGGCGGATGCCGGCACCCGCGAGCGGACGGCGCTCTCGCTGCTGAACGATCTCGACATCGCCGAAAGCTGCGGATCCTCGGGCGTCGTCGTGCATTTCGGCGTCTACAAGGACGGCGACCCGCTGGAAGGGTACAAGCTGATGATCCGCACGCTCGACTTCATCACCGAGCGCTGGGACGGCCGCTGCCGGCTGCTGATCGAGAATCAGGCGGGCAACCACGGCTTCATGGGCATGACGATGGAGGAGCTGGCGCAGGTGCTGGCGCTGTGCCGCGAGCCGGACAAGCTCGGCATCTGCATCGACAGCTGCCATCTGTTCGCGAGCGGCGTCTGGGATGGCGGCGAGCAGCCGGCATGGTCGGTCTCCGCGGCCGGAGCCGCGGCGCGGGGGCAGGTGCGAGCGCTTCATCTCAACGGCTCGGTCTACCCGTCCGGCTCGCGCAAGGACCGGCATGCCCGGATCGGCGAGGGCGAGCTCGGACTGGCCGGGCTCGGCTGGCTGCTGCGCCATTTTCCCGGCGTGCCTGCCGTGCTGGAGACGAGCCAGGACGACGGCGGCGGCTACGAGGGCCAGCTGGAGCGGCTGCTCGGCGCGGAAGCGGAGGGCCGGCGATGAACCGCTGCGGCAAGAAGATCGACCTCGAGGAGGGATGCCCATGACGGCCGTCATGGAGCTGGACCGGCTGCATCTGCAGCGGGACCAGCGGACGATTTTGAACGAGGTCAGCCTGCGGATCGGCCGCGGCGAGCAGTGGGTGCTGCTCGGCCGCAACGGCTCGGGCAAGACGACGCTGCTCGAGATGATGACCGGCTATCTGTTCCCGACGAGCGGCACGCTCGACGTGCTCGGCTTCCGCTATGGGGAATGCGACGTGCGCGAGGTCCGCAAGCGGATCGGCTATATCAGCCAGTCGCTGCTCGAGAAGCTGGCGCTCGCCGATCCCGTCTGGGAAGTCGTGGCGACGGGCGAATACGCTTTCCTGCGCTTTTATCAGGAGATCGACCCCGCTGTCAAAAGCAAGGCGCTCGCCCAGCTCGAGCGGGCGGGGCTCGCCCATGCCGCCGAGCAGCCGCTCGGCACGCTGTCCCAGGGCGAGCGCAAGAAGGTGCTGCTCGCCCGCGCCCTCATGAGCTCGCCGGAGCTGCTCATTCTCGACGAGCCGTGCTCCGGTCTCGATCTGCATGAGCGGGAGAAGCTGCTGGCGTCGATCGCCCGGCTGACGGACGAGCGGATGACCGTGCTGTATGTGACTCACCATATGGAAGAGATCCTGCCGCTGTTCACCCATGTGGCGCTGCTGCACGAGGGCAGCCTGCTTCATGCAGGCCCCAAGGAGCAGGTGCTGCGGAGCGACGTGCTCTCGCAGGCGTATGAGGCGCCGATCGAGGTGGATTGGGATTACGGCAGGCCATGGATAAAAGTAAGAGCGGATGGTGTAGAGAATTGACCGTTTGGATAGGTACCGCCAACAAGCAATACGCCTCCTATGCGATGGAGGAGCTCCGCCGGCAGTTCGAGGGCATGTCGCTCTCGCAGCTGTCGCCGGGCGAGACGTTTCTGATGCAGCTGCCGCAAGGGCGCGATGAGGTGCTGGAGTCGATCCAGGCCCGCAAGCCGATCTTCCTGCGCCATCTGCAGCCGGTCGACGCGTCGCGCGCGATGTCGCTCGACGCCGACGACCTCGACTGGCTGAGCGACTGGCTGCGGCTCGCGCGCGGCCAGCTCGCCGGCCAGCGGGTCGGCGTCCATATCCGCAAGGCGGAGGGCAGCCCGTTCCCTTACTCCGCCGCCGACGCGCGAGCCGTGCTCGACGCCGTGCTGGCCGAGGCGGGAGCGGAGCCGGCGCACAAGCAGCCGGATGCGCTCGTCGCCGTCTACGCGTCGCGCGATACGCTGTATGCGGGCATCGGCACGCCGCAGGAGATGCTGAGCGACTGGCCGGGTGGAGCCGTCCGCTTCCAGCGCGAGGACGGCCAGATTTCGCGGGCCAAGTTCAAGCTGCTCGAGGCCGAGCGCGAGTTCGGGCTCGACTACTCGCGGTACTCGCGGGCGCTCGACATCGGCGCGGCGCCGGGCGGCTGGACGTCGCTGCTGCTCGAGCGCGGGCTCAAGGTGACGGCGGTCGACCCCGCCGAGCTCCATCCCTCGCTGCAGGCGTACCGGACGTTGACCGTGCTGCGCAAAAACGCCTCCGAGGTCAAGTTCGCCCCGGGCAGCTTCGATCTGCTCGTCTGCGACATGAGCTGGAGCCCGATGCAGATGTGCCGGCTCGTGCTCGATCTCGCGCCGGCGCTGCAGAGCGGAGGCACGGCGATCGTCACGATCAAGCTCATGCACCGCAAGCCGCTGCAGACGATCCGCGAGGTGATGCAGCGCTTCGGCGAGGCGTTCGAGATCGTCGGCGCGCGCCAGCTTTTCCACAATCGGGAGGAAATGACCCTCTGCATGACGAAACGATAAGATAATAAGAACGGCATCATTCAAACGGGAAAGCATCCCGCATGCCGGCAGACTCTCTATGGGGAGAAGTCTGCCTGCGGCGGGATGCTTTTTTTCATTCGGGAAAGGGGAATCGGCATGCTGCGGAAGAAAGACGGAAGACGGGCGGGGCTGGCGGCGGAGACGGAGGCGCTCGGCCAGCGGGAGGAAGACGGCTGGCTGCAGCCCGGCGACGTGCAGGGAGGCCGCTACCGCATCCTCAGCCTGCTCGGCAAAGGAGGCATGGGGGAAGTGTATGCGGCCGAGGACCTGCGCCTCGGGGGCGCGCTGCGGGCGCTCAAGCTGAAGCCGGCCGGAAGCTGGAGCGAGCGTCCGAGCGCCGACGAGGCGAGGCTGCAGATGAAGCTGGAGCATCCGCATCTGCCGCGTCTGTACGATTATTTCCCTGCGGAGGGAGGACAGCCGGAAATGCTCGTCATGGATTATATCGAAGGCTGCACGCTGGAGGAGGAGGCGCGGGCCAGGCCGGACGGCTATACGGCGCTAGAGGCGGCCGCCGCGGCGCTGCAGCTGTGCTCCGCGCTCGCCTACCTGCACGAGCAGCGTCCGCCGATCATCCATCGCGACCTCAAGCCGGCCAACGTGATGGCCGCGCGCTCCGGGAAGCTCATGCTGATCGACTTCGGCATCTCCCGCCGCTTCTCGCCCGAAGCGGCGTCCGACACGACGCAGCTCGGCACGCCCGGCTATGCGGCGCCGGAGCAGCTCGCCGGCGAGCAGAGCGATGCCCGCACCGACATGTACGGGCTCGGCTGCCTGCTCGTGCGCCTCATGCGCGGCGCGCTCCCTGGACGGCGCGGACACGAGGGGCGGGCGAGGGAGCTGCCGTACTGGCTGACGCGGCTGCTGGAGGAGGAGCGCGGCCGCCGCTACGCCAGCATGCGCGAGGCGGAGGCGGCGATCCGCAGCTGGCTGGAGGCGGAGGGAGAGGCGCCGGCGGCCGGCGGCCTGCCGTCGTTCGCCGCGCCGACAGACGCCTTCCCGGCGGGGCTGCCGCGCGTCGCGGCGCCGGGCAGGCTCTCCGTGCTGTCGCTGTCTCCGGGCAGCGGAGCGACGTTCGTCTGCCTCATGCTGGCGCGGCTCGCCGCCGAGCGCGGCTGGCCGGTGCAGGCGGCCGAGCTCGACGGCGTCCGTCCGCATTGGCGGACGCTGCTCGGAGCGCCGGAGCCGCTGCCCGCTGCGCTCGATCCGCGTTTCGGCCGCTGGCTGCAGGACGGCGTCGAATGGCTGCCGCGGCTGGCTGCCGCTCCAGGGCTGGAGCGGGACGAGGCGGCGGCGAGGCTCGACCTCATGCTGAGAAGCCGCGCCGGGGCGCTGCAGCTGCTCGACTGGTCTTCCGGGTGGACCGGGGACGAAGCGCTGCGAACCGTCGCCGCCTCGGCGGCCGTCATCGTCGTCGCCGATCCCGATCCGTCCCGCTGGAGCCGCGAGCGCCTGCAGCGGCTGGAGGAGCTGACCGCCCGGCTCGGACCGGACCGCATGCGCTGGGTCGCCAACAAGGACGTCCGCTTCGCGGGAAGGCGCGAGTGGCTCGACCTGCTGCCGGCCCGGCCGGACGCCCAGATGCCGTTCCTGGAGCCGGAATCGTGGTACGAGCTGCTCTGGCAGGGCTTCCCGCTGCCGCGGCGCGGAGCGGCGGCAGCGGCGGTGCGCGGAGCGTTGTCGCCGCTTCTGGAGCGTCTCGCCGCGAAGCTGCACTTTTAGCTCGGGAGGGGGAGCCAAGAAGGGGCGGTTTATGGTACAATCACCTATTAGGGGCCGCTGATCCGGTTTCCTTCGCATTTCAAAGGAATGGAGAAATCAACCACTCATGAGCTTACTCACCGTAGAAAATTTATCGCATACATTCGGAGACCGCATCCTGTTCAAGGAGGTCTCCTTCCGCCTGCTCGCAGGCGAGCGGGTCGGCCTGGTCGGCGCCAACGGCGCGGGCAAGTCGACGCTGATGAACATCCTGACCGGCAAGCAGCTCAAAGACGAGGGCCGCGTGGAGTGGACGCCGAAAATCCGCTACGGCTACCTCGATCAGCATACGAAGCTCGAAGCCGGCAAGACGATCCGCGACGTGCTGCGCGACGCCTTCGCGCCGCTGCTCGTGCTGGAGCAGGAGCTGTCCGAGGTGACGGCCGCCATGGGCGAGCCGGACGCCGACCTGGACGCGCTGCTGGAGCGCATGGGCGAGATCCAGGAGGAGCTGGAGATCGGCGACTACTACATGCTCGACGTCAAGGTCGAGGAGATGGCCAACGGCCTCGGACTGAACGCGATCGGCCTCGACCGCGACGTCACGGCGCTGAGCGGCGGCCAGCGCACCAAGGTGCTGCTCGCCAAGCTGCTGCTCGAGAAGCCGACGGTCCTACTGCTCGACGAGCCGACGAACTATTTGGACGAGGAGCATATCACCTGGCTGGCGGGCTATCTGCGCAACTATCCCAACGCCTTCCTCCTGATTTCTCACGATACGGGCTTCATGAACTCGGTCGTCAGCGTCATCTATCATCTGGAGTTCGCGCGGCTGACCCGCTATACGGGCAACTACGAGAAGTTCCTCGAGATGGCCGAGCTGAATAAAGCCCAGCATCTGGGCGCATACGAAAAGCAGCAGGACTTCATCAAGAAGCAGGAGGACTTCATCCAGCGCAACAAAGCCCGCGCGTCCACCTCGGGCCGGGCCAAGAGCCGGGAGAAGCAGCTCGACCGGATCGAGCGCATCGACAAGCCGGAGGAGGCCGCCAAGCCGACGTTCAAGTTCAACGAAGGGCGCACGAGCGGCAAGACGATCTTCGAGGCCAAGGGGCTGCGCATCGGCTACACGAAGCAGCTGCTGCCGGAGATGGACATGCTGATCGAGCGCGGCGACAAGATCGCTATCGTCGGCTGCAACGGCGTCGGCAAGTCGACGCTGCTCAAGACGATTCTCGGCCGCATCGAGCCGCTCGGCGGCGAGGTGTATCGGGGCGACTACCTGCTGCCGGCCTACTTCGAGCAGGAGGCCAAAGCTCCGACGATGACGCCGCTCGACGACGTCTGGAACGAGTTCTCGGGCATGAACCAGCATGAGGTGCGCGCGGCGCTCGCCCGCTGCGGCCTCAAGAACGAGCATATTACCCGCGCCCTCAACCAGCTGAGCGGCGGCGAGCAGGCCAAGGTCCGGCTGTGCAAGCTGATGCTGCGCGAGAGCAACTGGATTCTGTTCGACGAGCCGACGAACCATCTTGACGTCGTCGCCAAGGCCGAGCTGAAGCGCGCCCTCGAAGGGTATCGCGGCACGGTCGTGCTCGTCTCGCATGAACCGGATTTCTACGAGAGCTGGGTGACCAAGACGTGGGACGTCGAATCGTGGTCGCTCAAGCAGGCTCAAAGCTAGCTATCCAACCGGAAAGCAGGTGACATCCAAGAATGAATGAACGCGTCCTGGTAATCGAAGACGAAGAGAGCATCGCCCGCATCCTCCAGCTCGAGCTGGAGCATGAAGGCTATGAGGTCGGACATGCCGCGGACGGCCGCAGCGGCTTCATGCAGGCGACCTCCGGCGAGTGGGACCTCGTCCTGCTCGACGTCATGCTGCCAGAGCTCAACGGCATCGAGGTGCTGCGCAGGCTGCGGCAGGCCGGCAATCCCATTCCCGTCATTCTCATCACGGCCCGCGATACGGTTCCCGACAAGGTAAGCGGCTTTGAGCACGGAGCGAACGACTACGTGACCAAGCCCTTCGCCATGGAGGAGCTGCTCGCGCGCGTGCGCAACCTGCTCCGCATTTTCCAGCAGAATCCCAAGGAATCCGAAGGCTCCGACCTGCTCAAGATCGGCGATCTGACGGTCGAGCTCCGCACCCGCAAGGTGTTCCGCAAGGAGCTCGCGATCGATCTGACGCCGCGGGAGTTCGAGCTGCTCGTCTACCTCGCCCAGCATAAAAACGAGGAGAAATCCCGCGAGGAGATCCTCTCCGAGGTGTGGGGCTACGACTTCATGGGCGAGACGAATCTCGTCGACGTCTATATCCGCTACTTGCGCCAGAAGCTCGACAAGGGCTTCCGCCACAAGCTGATCCATACGGTGCGCGGCGTCGGCTACATGATGAAGGAGCCGGAGGCATGACCCTCCGCAAGCGATTCACGCTTTTCACCATCTTTTGGCTCATCTTCATCCTGATCCTGTTCAACATCTTCGTCTATCTGTTCATGACCAAGATCACGACCCGCAGCGAGCAGCAGGTCATGACGAACAAGGTCAACCTGATCCTCGAGAACAACAAGATCATGGACAAGGACCATCTGTCCGACGAAGGCCTGCTGCGGGAGTTCTACAACGTTAACGAGCTGATCCGCATCATCACGCCCGACGGCAAGACGGTCAACCTGCAGGGCTCCGACACCGACCTGCTCGCGCTGCCGGTCAAGTTCGAGCCGTACCATGTGCAGGGGGAGATGTTCGTCGGCAGCACGCGCGTCCTGTACATGAAGGTGCCGCTGTACGAGGATTCGGAGATCATCGGCATGCTTGAGATCGAGCGCAAGCTGAACCTGCAGGACAGCTACATGAAGGTGCTCGTCGCCGCGCTGTCGGTGACGAGCATCGGGGCGATCCTGTTCGCGATCTTCGGCACATTCTGGTTCACCTCGCGCCTGACGGCGCCGATCCAGCACATGGTGCAGACGATGCGCGAGATCGACCGCAGCGGCAAGCTGCGCAAGATCGAGATCGGCGACAAGGAGGAGTCGGCGGAGCTGCTGCAGCTTATCCGCGCCTTCAACCAGATGATCGAGCGGCTCGACCGCACGTTCGCCCGTCAAAAGCAGTTCGTCGCCGACGCCTCGCATGAGCTCAAGACGCCGCTGACCGTCATCAGCAGCTACGCCGGCATGCTCAAGCGCTGGGGCCGCGACGACGTGAAGATCCGCGACGAGGCGATCGAGGCGATCGCCAAGGAGTCGGAGCGGCTGCAGAACCTGACGAAGTCGATGCTCATGCTCGCCGAGGCGGAGCAGGAGGACTGGCTCAGCCTGCAGACGTTCGACGTCGTGCAGATGGTGGACGAGCTGGCTTCGATGCTGCAGCTGACGTTCCAGCGCCAGATCCGCGTCCATACGTCCGCCGGAGGGCTGCGGATGTCCGGGGACAAGGACAAGATCCGCCAGCTGCTCGTCATCCTGCTCGACAACGCGATCAAGTACAGCAAGGAGCCGATCGACGTCACGGTCAGCTCGGTCAAGCAGTCGGTGCGCATTCATGTGACCGACAAGGGCATCGGCATCGAGGAGAACGAGATTCCGCATCTGTTCGAGCGCTTCTACCGCGTCGACGGCGCGCGCCGCCGCACGACCGGCGGCGTCGGACTCGGCCTGTCGATCGCCAAGCGCATCGTCGACCTGCATGAAGGCCAGATCGACGTGTTCAGCAAGCCCGGCAAGGGCACGACGATTACGCTGCAATTTCCGCAGACGCTCAAAAACACGTCCGGCCGCTGAGCGGCCAGACGTGTTTTTTGCGCCGGCGCCTGAACGCCTGGTGTCAAAAACGCCTGGTACCCAGAAACGCCTGATGCCCAAAACGCCCAAACGCCTGGCGCCTGAGCGCCTAATGCCCAAAGCGCCTGTCGGCGCACGCAAGCCTCCGGGCGCCAGCTTGCAAAGCTGGGCGCCCGGAGGCTTCGATGCGAAGTCTTCGATGCGAATTACAGCACGCGTTTGGCGGTCACATAATGCTTGTTCCAGTACGAGGTGCCGAGACTGGAGACGGTGACGCCCGTCTTGCCGTATGTATGCAGGATCTTGTTCGAGCCGGCGTAGATGGCCACATGGCCGATGCCTTTGCCGTTGCTGTTCGTGAAGAATACGAGATCGCCTTTGCTCAGGTAGCCGCGGGCGACCTTATCGCCCTTTTGCGCTTGCTGCGACGACGTGCGGGGGAGCGTGATCCCGTTTTTCTCGAAGACGTATTGAGTGAACGAGGAGCAGTCGAACGCGTAGGTGACGCCGCTCGGGGCTCCGAGCCGGTAAGGAACGCCAAGGTACTGCTTGCCGTAATCGAGAAGCTTCTCCGACTCGGGCGTAGCGGCCGAAGCCGTTTGAAGCGATCCGATATGGATGCCAGCCACGCCGATAGCAGCACAGAGGCTGAGGCGGGCGATCGTTTTTTTCCAGTTGCTCTTGCGCATATCTTGTGGTGTCCCTCCATCATGGTGTACGGTGTACTAGGGTGTTTTTCGACTGAGGCTACTATACCATACGGGGAGCAGCCTAATTTCTGCCAGTAAGAGCAGGATGCCTGTTCTGGCGCGATTCCCCCGTCAATATGAGAACTTCGTGAGAATCTTCTCATGAAGGCGTTTCAAGGAGGCGATTTGCGGTGAAAGTGAGAGTTTCGGCGGTTCAATACCGCTTGGAGGATATCGGCAGCTTCGAGGAGTTCGCCGCCCAGGCGACGCATTACGTGCGCAATGCTTCGGAATATGGCGTGCAGATGCTGCTGTTTCCGGAGTTTCTGACGACCCAGCTGCTGTCGATCGGAGACGAGCAGGGAAGGCCGCTCGGCATCGGCCGCCTGCCGGAGTTCACCGAGCGCTACGAGCAGCTGTTCCAGGGACTGGCGGCCGAGTACGGCATGCACATCGTCGGCGGCACGCATGTCGTCCGCTCGGACGACGGCAAGCTGCGCAACACCGCTTATCTGTTCTACCCGGACGGCGGCATCCGCACGCAGGCCAAGCTCCATCTGACGCCGACCGAGGTCGAGGAATGGAACATGGCTCCGGGCGACGGGCTGGAGGTGTTCGAGACGCCTTTCGGCACGATCGCGATGCTGACCTGCTACGACATCGAGTTTCCGGAAATCGTGCGCATGGCGCGGGCCAAGGGCGCCGACGTCATCTACTGCCCGTCCTGCACCGACGACCGCCACGGCTTCTACCGCGTCCGCTACTGCGCGCATGCGCGGGCGGTGGAGAACCAGGTGTACATCGTCACGACCGGCACGACCGGCTCGCTGCGCCGCGTCGACTTCATGCGCGCCAACTACGGACAGGCCGCCGTCCTTACGCCCAACGACATTCCGTTCCCGCCGCGGGGCATCCTGTGCGAGGACGACGACAATCAGGACATGCTGATCGTCGCCGATCTCGACCTGCAGCTGCTGGAGGACGTGCGCCGGGCCGGCTCGGTGACGACGTGGCGCGACCGCCGCACCGATCTTTATCCGGACTGGTTCTGA

Protein sequences of DBSCAN-SWA_5

>NZ_CP045802|2820933:2831696|2820933_2821752_+|WP_028597653.1|DBSCAN-SWA
MPEYPEMDRYRVLLSDALAGQKIVSAEVGREKSLNVPADEFIRRVQGRAVWFVERRGKHLLLHLDSGERLLAHLMLGGWMFYGSEEEKPDRTVQVRLGFERGNLYFIGLRLGYLHLLSAREAEARLAELGPEPLDPKLTEERFAQRLLAKKRSALKSALVDQSVLAGIGNCYADEIAWQAEVRPGARIGSLEPATLSRLYASTQAVLTEAKTLGGYMEHPFRVGDETTGGYNSQCKVYDRPGEPCLRCGTKIVQEEQSSRKVFFCPSCQKEH
>NZ_CP045802|2820933:2831696|2828581_2829955_+|WP_028597659.1|DBSCAN-SWA
MTLRKRFTLFTIFWLIFILILFNIFVYLFMTKITTRSEQQVMTNKVNLILENNKIMDKDHLSDEGLLREFYNVNELIRIITPDGKTVNLQGSDTDLLALPVKFEPYHVQGEMFVGSTRVLYMKVPLYEDSEIIGMLEIERKLNLQDSYMKVLVAALSVTSIGAILFAIFGTFWFTSRLTAPIQHMVQTMREIDRSGKLRKIEIGDKEESAELLQLIRAFNQMIERLDRTFARQKQFVADASHELKTPLTVISSYAGMLKRWGRDDVKIRDEAIEAIAKESERLQNLTKSMLMLAEAEQEDWLSLQTFDVVQMVDELASMLQLTFQRQIRVHTSAGGLRMSGDKDKIRQLLVILLDNAIKYSKEPIDVTVSSVKQSVRIHVTDKGIGIEENEIPHLFERFYRVDGARRRTTGGVGLGLSIAKRIVDLHEGQIDVFSKPGKGTTITLQFPQTLKNTSGR
>NZ_CP045802|2820933:2831696|2823398_2824448_+|WP_153783530.1|DBSCAN-SWA
MDKSKSGWCRELTVWIGTANKQYASYAMEELRRQFEGMSLSQLSPGETFLMQLPQGRDEVLESIQARKPIFLRHLQPVDASRAMSLDADDLDWLSDWLRLARGQLAGQRVGVHIRKAEGSPFPYSAADARAVLDAVLAEAGAEPAHKQPDALVAVYASRDTLYAGIGTPQEMLSDWPGGAVRFQREDGQISRAKFKLLEAEREFGLDYSRYSRALDIGAAPGGWTSLLLERGLKVTAVDPAELHPSLQAYRTLTVLRKNASEVKFAPGSFDLLVCDMSWSPMQMCRLVLDLAPALQSGGTAIVTIKLMHRKPLQTIREVMQRFGEAFEIVGARQLFHNREEMTLCMTKR
>NZ_CP045802|2820933:2831696|2824532_2826191_+|WP_153783531.1|DBSCAN-SWA
MLFFIRERGIGMLRKKDGRRAGLAAETEALGQREEDGWLQPGDVQGGRYRILSLLGKGGMGEVYAAEDLRLGGALRALKLKPAGSWSERPSADEARLQMKLEHPHLPRLYDYFPAEGGQPEMLVMDYIEGCTLEEEARARPDGYTALEAAAAALQLCSALAYLHEQRPPIIHRDLKPANVMAARSGKLMLIDFGISRRFSPEAASDTTQLGTPGYAAPEQLAGEQSDARTDMYGLGCLLVRLMRGALPGRRGHEGRARELPYWLTRLLEEERGRRYASMREAEAAIRSWLEAEGEAPAAGGLPSFAAPTDAFPAGLPRVAAPGRLSVLSLSPGSGATFVCLMLARLAAERGWPVQAAELDGVRPHWRTLLGAPEPLPAALDPRFGRWLQDGVEWLPRLAAAPGLERDEAAARLDLMLRSRAGALQLLDWSSGWTGDEALRTVAASAAVIVVADPDPSRWSRERLQRLEELTARLGPDRMRWVANKDVRFAGRREWLDLLPARPDAQMPFLEPESWYELLWQGFPLPRRGAAAAAVRGALSPLLERLAAKLHF
>NZ_CP045802|2820933:2831696|2826297_2827854_+|WP_028597657.1|DBSCAN-SWA
MSLLTVENLSHTFGDRILFKEVSFRLLAGERVGLVGANGAGKSTLMNILTGKQLKDEGRVEWTPKIRYGYLDQHTKLEAGKTIRDVLRDAFAPLLVLEQELSEVTAAMGEPDADLDALLERMGEIQEELEIGDYYMLDVKVEEMANGLGLNAIGLDRDVTALSGGQRTKVLLAKLLLEKPTVLLLDEPTNYLDEEHITWLAGYLRNYPNAFLLISHDTGFMNSVVSVIYHLEFARLTRYTGNYEKFLEMAELNKAQHLGAYEKQQDFIKKQEDFIQRNKARASTSGRAKSREKQLDRIERIDKPEEAAKPTFKFNEGRTSGKTIFEAKGLRIGYTKQLLPEMDMLIERGDKIAIVGCNGVGKSTLLKTILGRIEPLGGEVYRGDYLLPAYFEQEAKAPTMTPLDDVWNEFSGMNQHEVRAALARCGLKNEHITRALNQLSGGEQAKVRLCKLMLRESNWILFDEPTNHLDVVAKAELKRALEGYRGTVVLVSHEPDFYESWVTKTWDVESWSLKQAQS
>NZ_CP045802|2820933:2831696|2822643_2823435_+|WP_043110951.1|DBSCAN-SWA
MTAVMELDRLHLQRDQRTILNEVSLRIGRGEQWVLLGRNGSGKTTLLEMMTGYLFPTSGTLDVLGFRYGECDVREVRKRIGYISQSLLEKLALADPVWEVVATGEYAFLRFYQEIDPAVKSKALAQLERAGLAHAAEQPLGTLSQGERKKVLLARALMSSPELLILDEPCSGLDLHEREKLLASIARLTDERMTVLYVTHHMEEILPLFTHVALLHEGSLLHAGPKEQVLRSDVLSQAYEAPIEVDWDYGRPWIKVRADGVEN
>NZ_CP045802|2820933:2831696|2827886_2828585_+|WP_028597658.1|DBSCAN-SWA
MNERVLVIEDEESIARILQLELEHEGYEVGHAADGRSGFMQATSGEWDLVLLDVMLPELNGIEVLRRLRQAGNPIPVILITARDTVPDKVSGFEHGANDYVTKPFAMEELLARVRNLLRIFQQNPKESEGSDLLKIGDLTVELRTRKVFRKELAIDLTPREFELLVYLAQHKNEEKSREEILSEVWGYDFMGETNLVDVYIRYLRQKLDKGFRHKLIHTVRGVGYMMKEPEA
>NZ_CP045802|2820933:2831696|2830161_2830644_-|WP_028597660.1|DBSCAN-SWA
MRKSNWKKTIARLSLCAAIGVAGIHIGSLQTASAATPESEKLLDYGKQYLGVPYRLGAPSGVTYAFDCSSFTQYVFEKNGITLPRTSSQQAQKGDKVARGYLSKGDLVFFTNSNGKGIGHVAIYAGSNKILHTYGKTGVTVSSLGTSYWNKHYVTAKRVL
>NZ_CP045802|2820933:2831696|2821754_2822603_+|WP_028597654.1|DBSCAN-SWA
MSRFGRLGCHVSTRGGYRAAAERAAAIGCGSFQYFPKNPRSLGVKAFDRGDAGRCREFCVERGIESIAHSPYPCNLASADAGTRERTALSLLNDLDIAESCGSSGVVVHFGVYKDGDPLEGYKLMIRTLDFITERWDGRCRLLIENQAGNHGFMGMTMEELAQVLALCREPDKLGICIDSCHLFASGVWDGGEQPAWSVSAAGAAARGQVRALHLNGSVYPSGSRKDRHARIGEGELGLAGLGWLLRHFPGVPAVLETSQDDGGGYEGQLERLLGAEAEGRR
>NZ_CP045802|2820933:2831696|2830835_2831696_+|WP_153783532.1|DBSCAN-SWA
MKVRVSAVQYRLEDIGSFEEFAAQATHYVRNASEYGVQMLLFPEFLTTQLLSIGDEQGRPLGIGRLPEFTERYEQLFQGLAAEYGMHIVGGTHVVRSDDGKLRNTAYLFYPDGGIRTQAKLHLTPTEVEEWNMAPGDGLEVFETPFGTIAMLTCYDIEFPEIVRMARAKGADVIYCPSCTDDRHGFYRVRYCAHARAVENQVYIVTTGTTGSLRRVDFMRANYGQAAVLTPNDIPFPPRGILCEDDDNQDMLIVADLDLQLLEDVRRAGSVTTWRDRRTDLYPDWF

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_028597653.1|2820933_2821752_+	Fpg/Nei family DNA glycosylase	G3MA33	Bacillus_virus	5.0e-16	26.5
WP_028597654.1|2821754_2822603_+	deoxyribonuclease IV	A0A1V0CP95	Kaumoebavirus	4.1e-05	30.3
WP_043110951.1|2822643_2823435_+	ATP-binding cassette domain-containing protein	F2Y2R6	Organic_Lake_phycodnavirus	2.9e-13	30.2
WP_153783530.1|2823398_2824448_+	SAM-dependent methyltransferase	NA	NA	NA	NA
WP_153783531.1|2824532_2826191_+	protein kinase	A0A291AU40	Pandoravirus	1.1e-12	31.9
WP_028597657.1|2826297_2827854_+	ABC-F family ATP-binding cassette domain-containing protein	A0A2K9L3Z8	Tupanvirus	1.4e-54	29.6
WP_028597658.1|2827886_2828585_+	response regulator transcription factor	W8CYM9	Bacillus_phage	1.7e-33	33.8
WP_028597659.1|2828581_2829955_+	HAMP domain-containing histidine kinase	A0A1V0SGX0	Hokovirus	6.9e-18	28.9
WP_028597660.1|2830161_2830644_-	glycoside hydrolase	NA	NA	NA	NA
WP_153783532.1|2830835_2831696_+	acyltransferase	M1H2P4	Paramecium_bursaria_Chlorella_virus	2.6e-07	27.2

Sequences of DBSCAN-SWA_6

Nucleotide sequences of DBSCAN-SWA_6

>NZ_CP045802|4288697:4359054|DBSCAN-SWA
ATCAGTCCGCCGTCCGCAAGCCGTCCGGCAGCAAAGCGTTCAGATCGGCCATGCCGACCGCCAGATGGATGCCGGCCATCGTGCGCAGCGAGCCGGAAATGATCCCGGCCAGCCGCCCTTGCTCGTCGAGCAGCGGACCGCCCGACATGCCGCTCGCGATGGCGGCGTCGATCAGCACGCGGCTGCGGCCGCTCACGACCGCGTCCGGGCTGCTGACGATGCCCTGCGTCACGATCGGCGTCTGCTTGAGCGGATAGCCGATCGCATAGACGGCGTCGCCATGCTCCAGCTTCTCCGCGCGCCGGGCGACGAACGGATAGCCGCCTCCGCTTTTCGGAGCGGGCAGCTCCAGCACGGCCGCATCGGTCCGCTCGTCGTAGCGGACGACCTTCACCGGTGAGACGGTCTTTCCGTCCGCGAGCACCGCCTCCAGCTTCGCCGCGCCCTTCACGACATGATAGGCGGTCGCGGCATCGCCCCTCGCGGAGAGCAGCACCCCGGTGCCCGTCGCGCCGACGGTGCCGTCGGCTCCGAGCGCCCTCAGGTAAAACACGGCGCTCGAGGCGAGCCGGTAGCTGTCATCGGCCGCCAGCGGCGCCTGCCGCTCCGCCTGCGTCGTGCCTGCCGCATACGGCCCTGCCGCCAGCACGGCGGCTAGAGCCAGGACGGCGATCCATCCTTTTTTCATCGCTTAACTTCCTTTCCTGGATCGGAAATCATGCCTGGCCGGACGGCCGGCTCAGTCGCGGGCTGCGGCCATGATGTCGGCGTACGCCCAGTGGCTCGGCGGCACGTCGCCATAATGCGGCCCGGCGTCCGCGCGCTTGGCCGTGCCGGCCATGCGGTTCAGCAGCGAGATCGCCTGCGCGCGGGTGAGCGGGCTGTTCGGACGGAAGCTGCCGTCCGGGAAGCCCTGGATATAACCCGCATCGGTCAGGGCGGCGATGAAGCTCGACGCCCAGTGCTTGCGCGCATCCTTCTGCTTCGGCACGGCATCGCCGTCGACGCTGATCTGGAGCGCCCGCGCGGCGATGACAGCGAACTCCGCCCGCGTCAGGCCGCGGTCGCCGCCGAACGTGCCGTCCGGATAGCCGCCGACGATGCCGGCGGAGGCGAAGAAGGCGACGAGCTGGTCGCTGCGTCCCGACTTGTCCGGGAAGGCGTTGTACAGCTCGCCCTCCTCGCGGTCAAGCAGCGGCGCAAGCGCTTCGATCAGCTCGTAGCGGCTCATCGCCGCGTCCGGCTTGAACATGCCGTCGGCATAGCCGGAAGCGTAGCGCACGGTCGAGGCATCCTTGCGCAGGCTGTACTGCGCGGCGCCGACGTCGAACTTGTACGTCAGGATGCGCTTGTCGCCTTCGACGAGCGCTTTCACCGTCACGGAGCGGTTCAGCACCAGCTCGCCGGTGAAGCGCGGGCTGGACTCCGTCGGGTCGCTGCCGTCGGTCGTATAGCGGATCCACTTGCCCTCCGGCGCGGTCAGCCGCAGGATGCTGCCGCGCGGCGCGCGCACGGCGGCGGGCTGCTCGTCGCCGATCGCCGGCTTGCCGATGTTCGATTCGACGGCAGGCTTAGGCTCAGGCGTCGGAGACGGGCTCGGCGCCGGGAAGAAGAACCCTCCTCCGCCCGACGGCGATGAAGGCGGCTGCAGCTTCCACTCGCCGCTCAGCGCCGGGCTGTGCTCCTTGCCGAGCACGACTGCGATCGCCTTCAGCGTCGTCGTCGCCTTGAGCAGGATCGGCGACGAGTAGACGGCCGATTGCTCGCTCGGCTCGCTGCCGTCAAGCGTGTAATGGATGACGGCTCCCGGCTCGGCGGACAGGTCGATCTCGACCTTCTCCTTGAACTCCCGATCGCCCGAGACGACTTGCGGAGCGGCTGCGGCCTGCGGCCAGCGCAGCTCCGGCGCGTTCAGGACAATCGTACGGGCGAAGCCGCCCAGCGAGGCTTGGAGCTCGGCGACGCCGTCGGCCAGCAGCCGGCCGGAGCCGGAATGGAGCTGAACGAGCGACGGATCGGCGCTCCAGAGGAGGCCGTCCGCCCGGCTGAGGCCGAAGCCTGCCGTCAGGCGGTTGATCGTGTCGCCGGCCGCCGGCATGACGGCCGCGGCCGCCAGGCGGGCGAGCGGGCTGTCGGACGGCGCCGGATAGAAGCCGGCCGCTGCGCGCCAGACGCCGCCGGACAGGCCGGACGGAAGCGTGCCGCTCGTCAGAGCCGCGCCGTCAAGGCCGCCCTCCGTGCGGATGATGCCTGCGGCGTCGTAATAAGCGACGCCGCGCTTGACCAGCTGCCGGTGGAACGACGCTCCGGCAATCTTGCCGCCGTCCGCCAGCTGCCCGGCGAGGCCGCCGAAGAAGCTGCGTCCCGGCACGAGCGCGCCCTGGATCGAAGCGACCGCTTCGCCGCCCGCGACGGAGCGCTCGACGGCGCCTGCGCTGCGGCCGGCGAGGCCGCCCGCCCAAGCGAGCGCCGTGCCGTCCGCCGTCGCCCTTCCGGACGCCAGCGTGTCGGAGATGCGGCCGTCGTTGCGTCCGGCCGCGCCGCCCGCGGCGGCTTCCGCGCCTTTGGACGACGCATCGGCCGCGCTGTACGAGCGCTCGATGACGCCGTCCTGGCGGTTGATGCCGGCGATGCCGCCGGCGCTGGCTTCGCTGCGCGCGAGGCCGGCGGCGCCGGACTCGGCGATGAGGCCGGCATTGTCGCCGACGATGAGGCCGGCGCTCAGGCGGCCGCTGGCCGAGCCTTCGGCCGTCGCGCCGCGAATGTCGCCGCCGGCCGCGTTGATGCCGGCGACGAGGCCCGCGTCGGCGCCGCTCGCCGAGCCCTCGGCCGTGACGTCGCGGAGCATGCCGCCCGATTCGTTGACGCCGGCGATGAGGCCCGCGCCAGCGCCGCCGCTAGCCTTGCCCTCGGCCGTGACGCCGCGGATGTCGCCGCCGTCCGCGTTGATCGCGGCGACGAGGCCGGCATGACGGCCGGCCTGCACGCTCGCGCCGACGAGCTGCAGGTCGGCGATGCGGCCGCGGTTGACGAGCGCGAGCGCCGCGTCGCCGCTGCCGCCGTCGGCGCGCAGGCCGATCAGCCGATGGCCGTCGCCGGCCAGCTCGCCGTCAAAGGCTTGCAGCGGCGTCCAGCCGAACGCGGACAGGTCGATGTCCGCCGTCAGCCGCAGCTTGTCGCCGGAGCCGAGCGGCGAAGCCGTGGCCGCGCGGTCGAACAGCTTGAAGTAGGCGGCGCCGGTGTCGTTGCTCAGCCGAACGTAGCCGTCCAGCTGCGCGCGGCTGCCGATCGCAATCTCGCCGTCTGCGGACAGGAGCAGGACGGACGGATCGTACGTCGCCGCCCAGCTGCCCGCCGGACGCGGATCGCGCGCCGGCACGGCCTCGGCCGAAGCCGCCGCCCCAGCGTTGCGTCCTACCGCCGCGCCGCTGCCGCTGTAGGCGGACAAGGCGATGCGGCCGTCGCGGAAGTTGTAGCCGACGAGCGCGCCTTTATGCGTGTCCGTGCCCTTGGCGCTGACGGTCAGCTCGATCGCGGACGCGTACGCCTGCTCGATCTTGCCGTCGTTGTAGCCGGCGAAGCCGCCCGTATACGAGCGGGTCGTGCCGGCGAGGCCGGTCGTGGCGACGCGCTCCTGCAGCGCATGGGAGCGAAGCACGCTGCCGCTGCGCTCGACGGCGGCCGCGAAGCCGCCGGTACGCGTGTCCTGGCCGGTGTTGCTGACCGAGCCGGACGCATAGCTGTCCTCGACGGCGAAGCGGTTGATGGAGCCGGCGAAGCCGCCCGCGTAGGAGCCGCGCTTGCCGGCAGCCGTCACCGCGCCGTCCGCATAGGCGTAGCGGATCGAGCCGCTGCCCGCGCCGTTCTCGCCGAGCTGTCCGGCGAAGCCGCCGGCATACAGCGTCGTGTCGATGTTGCCGTCAGCTACGTCGACCGGGATCGACGCGGAGCTGCGGGCGACGACGAGACGGTCGCCCTGGCCGAGCGCGCCGCCGACAAACGTCGCCGGGAGATTTTCCCCGATCGTCAGCGCCGTGCCGACCGCGATCCGCGATCCGCCGGCAGCGACGGCCCGGCTGTAGTGGATCTCGCCGTCCAGCGCGCGGCCGACAAGGCCGCCGACGCGGTAGACGCCGCTGCCGGAGGCGTCGATGCCGCCGAACGCATCGGCATGGACGAGGATGCCGCTGCTGAAGCCGGCGATGCCGCCCGCGTCGAGCTCGCCCGCCGAGCCGGCGGCGATATGCGCGCGGCTCGACGAGTCATAGATCGAGGCGCTGCGCAGCGCGCCGACGAGGCCGCCCGCATGCAGCGCGGATTCGCCGCCTGCGGCCGCCAGGTGCAGCTCGCCTTCGTACTCCGCCTGATACAGGCCGCGGTACAGCGGATAGAGGCCGCCGAAGCGCAGTCCCGCATCGCGGTCCGATGCGCTCAGCTCGCCGGCGATGCCGCCAGCCGCCAGCGCGCCGACGGAGCCGGCGTCGAGCGCGGCGGCGATCGGTCCGGACGCCTCGGCGTCCTGGATCGTCGTCTCCGCCGCGCGGCCGACGATGCCTCCGGCATAAACGGCCTCTCCGCGCGCGTCCAGCGACGCGAAGCTAGCCTTGACGCCGCCAAGCGCTGTCTGGTCCGCGCGGCCGATCAGTCCGCCGACCGCCGCCTCGTCCGAGCCGGCCGGAGCTTTTACGGCCAGTCCTTGGACCGAAGCGTCACGCACGTCCCAGGCCGCGATGCCGCGGCCCGTCTTTTCGCCGATCAAGCCGCCGGCAGAGCCGCCGCCCGTTACGCCGAGCGCGGACGGAGCCGCCTCGACCTTCAGGCCGCTGAGGCCGTTGCCGGCTGCCGAGCGGCCGATCAGACCGCCCGCCGCCGCATCGTCCGCGCCGGCGCTCACAGAGACCGCCTCGCCGAACGAGACGGACAGCTCCGAGGCGTCGCCGTCCGCGTAGGAGCCGAACAGGCCGCCCGCCGCGGAATCAATGCCGGAGGCTTCGACCGCGAGCCGCGTCAGCTCCAGCTTCAGCGCCGAGGAAGTCCCGCTCTGGCGTCCCGCCAGGCCGCCCGCCGCCGCCTCGTCGCCGGTTGCCGCGATGCGGCTGCCCACTTCGCCCGACGTCGTCAGGCTCCAGCTGCCGGCTGCGATCGCGGAGACGTTCTCGCCGGCGATGCCGCCGGCCGCTCCGCCCGCCGCCGCGCTCTCGACGCGGCCGCCGGCGAGCTCGGCCCGCAGGCTGTCCGCCGCGCCTTCGCTGCGGCCGACGATGCCGCCGGCGACGCCGCCGGAGACAGACGCTCCCGCAGGCAGCTTCAGCGCGATGTCGGCGATGCGGCCGTAGTTGAGGCCGACCAGCGCTCCGGCATACGAGGAGCCGCGCGCTTCCTTCGGCTCCAGCGCGAGGCCGCTCGCCGAGCCGTCCGCGCCGATGACGCCGAACAAGCCTCCGAACGGAACCTCGCCGCTGACGGCATAGCCGTCGATCAGATGGCCGCCGCCGAGCAGCTCGCCCTGGAACGCCAGCGCCTCGCTGACGCCGATCGGGCTCCACTGGGCGGACTGCACATGGATCGGACCTTTGATCTCGATCGTGCGGCCGGCGAAGCTGAACGGCTCGACGCCGACAAGCGTGCCGTTGACGATGGCCGCCAGACCTGCCAGTTCGGCCTCCGTGCCGATCTGGAACGTCGTCGCGTCCTTATCGCGCAAGTACCAGTTGAGGTTGGCGTTGACGTTGCCGCCCGTGCCCTCTTCCCCGCCGCCGCTGCTAGCCGCGCGGTTTACTTCCGGATATTGGTACTGGGCGCCAAGCGAGCCGTATTTCCAGGCGCCGGCAAAATCCCAGCCCGACAGCGCCGGAAACTCCGAGCGGTCCGACAGCGTCGACGACAGGATCGTGCTCAGGCGGCCGAGCACGCTCAGCCAGCGGTACTCGCCGTCGGCAAAGTCAGGCAGATCCTTGTTCAGGTTGAGCTTTTCGTCCTTGATGTAATAGCTCTTGTACAGCAGCTCCTTGCTCGCGTTGTCGTAGCGGCCGGCGAAGCCGCCCGCCAGCGCCGTCCCGCTCGCCGACACCTCGGCGGCGGAATAGCTCGACGAGATGCGGCCGGAGACGATCCGGCCGGCGAAGCCGCCGGCATACGAGCCGCTGCCCGAAGCCGTCACGCTCTTGGCGCTGTAGGCGTTTTTGACCGAGCCGCCCGCGAGCTCGCCGAGCAGGCCGCCGGCCTGCGCATAGGCGCCGGAAGCCGTCACCTTGGAGGCGGCGTACGACTGCTCGACCGTGCCGGAGCTGCGGCCGGCGAGGCCGCCGAGGAACACCGGCTGGCCGGACGTGCCGTAGGCTTTGCTCGTCAGATCCAGGTCCGTATAGGAGGCGAGGATGCGGCCGGCGTTGTCGCCGACGAGCCCGCCGGCCAGCGTTCCCTGGCCCTCGATCGTCAGACTGGCGTTCGTGTACGTGTAGTAGAGCGTGCCCGTCGCCGCGTTGCGGCCGACGAAGCCGCCGACGACGGCGTTCGCGCCTTTGGAGGAAACCGGAATCTTGTCCGTCACGCTGACGTTGGCGATCAGGCTGGCGTTCTCGCCGACGAGGCCGCCGACCGTCATGCCCGGCGCGAGCGCCTGCACGCTGCCGGATACGCGGCTGTTGACGATGACGCCGCTCGAGCTGGCCGGAGCGGCTGCCGGGTCGCTCGCGCGCGCCTCCAGCCGTGCCGCCATGCCGCCGACGAAGCTGCCGCTTGCGGAGGCGTTGGCCTTCAGCTGCATGCCGCCGAACACCGTATCGACGATCGCAGCACCCTCGCCGCCTTTCAGCGTGCCCGCCAGTCCGCCCGCCGCCGTATCCGGACCGCTCAGCAGCAAGCTCGCGCCGCTGCCGACGAGGCCGCGCAGCGTCGTCTCGACGCTGCTGCCGACCAGGCCGCCGGCCTTCGCCTGCGAGGCGTCCGCCGATGCGGTCAGGAGCAGGTTCTGCATATTCACGCGCTGCAGGTCGCTCTCGATCCGGCTGCTGTCCGCGCGGCCGGCCAAGCCGCCGGCCTCGATGCCGGGCGCGCTCAGCGTTAGCGCGACGTAGTTCGGCGCTTCCGCGAGCGCCGCCGGACGGATGAGATCGGCATGGACGGCGTAGCCGGCGATGCCGCCGATGCGCGCTCCCGCCGCCGTCGCCGCTGCCGTCGGCGACTCGCCGCCTTCAAGCTTCGAGTCGGTCAGCGAGGCGCGGCTGTCCGCCGTGCCTTCCAGCCGGCCGACGAGTCCGCCCGCTTCCGCGCCGGAGCCTCCGGCCGCAAGCGCGACGCTGCGCGCCGCGGCGCCGAGGATCGAGCCGCGGCTGAGGCCGGCCGCCCCGCCGAGCCGCGCGTCCGCGCCGGTCGAGCGGATCGTGACCGCCTCGGCCGCGCCGCCGCTCAGGCTGCCGGCGTTCTCGCCGGCGATGCCGCCGATGCGGGCGCGGGCGCCGGAAGAGTCAACCTCGAAGCCGGATACGAGCAGGCTCGCCTGAGCGGAGCCGTCAAGCCGGCCGATGCCGCCGCCAAGCGCGACTTCGTCGGCCGGCGCCTCCAGCGTGACCGCGCGGACCGCCAGCGGCTGCGCCGAGGTGCCGAGCACGGCCGCGCCGTCGATCCGGCCCGCCGCGCCGCCGAACGCGACTCCCGTCATGCCCGCGGGCAGAGCGGCGGATACCCGGTCGACCCGGCTGCCGCTTACCGTCAGCTCGCCGATGCCGCGGCCGATCAGGCCGCCGGCAGCGAAGTCGTCGCGTCCGCCCGCCGGCGAAGCAATCGCCGTCTCGAAGCGAAGGCTCGCCGAATCGGACGCAGACGGATCGCCGGCGCGAGCGCCTGCAATCGTGCCGGAGGCGGCGCCGGCGATGCCGCCGGCCGCGCTGCCGGAGCGCTGCGCCCGCAGCGTCAGCCAGGAAGCCGACGAAGCGGAGATCGTGCCGTCGGAATGGCCGGCGATGCCGCCCAGCTCGCCTTCGGCGACGATCGCGAGCGGCTGTGCCGCCGTGCCGCCGGCAGCGGAGCTGCTGATCTCGGCTCCCGCCGCCAGATAGCCGGCGATGCCGCCGGCATAAACGGCGCTGTCGCCGGACGTGTCGGCCGTCAGGCCGCTTTTGAACGACGCATGGCGGATCAGGCCGCCGCCGTTGTAGCCGACGATGCCGCCGGCGTATACGGCGCCCGTGCCTTGCGCCTCGACGGCGGCCGCCGAGACATACGCCGCAGGGTCATCGTCGGTCAGGCTGACGCCTTGCGCCGCATAGCCGAACAGGCCGCCGACATAAACGTCCTTGCCTTCGGCGGTGATCGGAATCGCCTGCTCGAAGCCTTTGGACCAGGTCAGCGCAGGGCCGACGAAGCCGGCGATCGTGCCGGAGTAGACGCGTTCGCCGCCGGCATGATGGACCGCGGCCGTCTGGCGCAGCGCGACGGAGGCGTCCGGCAGGACGCCGCCGATCGAGCCCGCCACGCCGCCGGCGTAGCTCTCTTCCGCATCCGGCGACGTCACGCTGACTTCGCCGCTGTTCGCCGTATCGGCCGAGAACGTCACCGGCGAGCCGTAATGCCCGGCGAGGCCGCCCGCATGCGCGAGCCGGCCGCCCGACACCGTCACGGCGCCGCCGTTGCGGATCGGAGTGCTCTCGCCCTGCATGTCGAGCGCCCCGGCCGTCAGGCCGGTCAGGCCGCCGGCGTACAGCTCGCTCGCGGCTCCGCCGCTCGCGGAGACCGCCCCGTCATTGGCCGCCTTTTTCAGCGTCAGGCCGCCCTCGGACACATGCCCGACCAGACCGCCGGCATAGGTGGAGCCCGCCACGGTTACGGACGCCTCGTTGAGCGCATTGGACACCTGCCCAGATCCCGAGCCGACGATGCCGCCCGCATAGGCGACGCCGGAGCCGCTCTCGGCCTCGATCGCAAGCTCGTTCTCGATATCGTAGACGATGCTGTAGCCGGTCATCTTGCCCACGGCCGAGCCTGCGTAGACGTTGCCCGCCACGGTGACGTCGATCTCGCCGTCCGCCTCGAAGCGGAAGCCGCCGACCGTGCCGCCGTCCATGTTGCCGACCAGTCCCTGATAAGGAATGGCGGCCGGAACGCGCATGCCGGAAATGCCGAACATCGCTCCGTCCTTGGCGATCAGCGTGCCCTTGAACGGATGGGATTCCGTGCCGATCGGCAGCCAGTCGTACGCCGACAGGTCGAGGCTCCGGTCGACCTCCAGAATTTTGCCCTTCAGGCCGTCCACGCCGTTCTCGCCGTTGACGAGCTTGGCGATGCCCGCCAGCTTGGCCGGCGTGTCGATCTTGAACGTCGTGTAGGTCGCGTCGAACCAGCTCGTATCCGCGGAGCCGTCCCAGGTCTGGGCTCCGGCTCCGGCCAGCATGGCCGTGCCGCCGGCGGCCCCGGCGAGGATGACGGCGCCGAGCGCCGCCATCCTCCAGGTCCGATATCTTTTCCTTGCCTTCATGTCCTGCCCCCCACTTAGATCCGTTCTTAGCAGACAACCCGCATCACGCCTGAAGCATGATGCGGGCTCGCCTGCCGGCCGGTTATGAATTCATCCAGTCGCTCGCCCGGACCGCGATCGCAGCCGCCTGGCTGCGGGTCAGCGGATCGCCCGGACGGATGCTGCCGTCGATGCCTTGAATGAGCCCCGCCTTGACGGCGGCCGCAACCGGGCCGCGCGCCCAGTCCGGGATCGCCTTGACGTCGGCGAAGGCGCCCAGCACGCGCGCGATCTCCGCTTCCTCAAGCTGCGCTCCCGGCTGCGCGATCGCCATCAGCCTGCCGGCCATGGCCATCGCCTCGAGCCGCGTCAGCGCCGCGTTCGGATCGTAGCGCTCCGCGCTCTTGCCGCTCGCCAGGCCGAGGCCGACTGCGATGCCGACCGTGCGGGCGTACCAGCTGTCCGCTGGCACGTCGCCGAAGCGGACCGCCGCGGCCGGCTCGTTCATGTAGCCTGCCGCGCGCAGCAGGATCGTCGGATACTCGGCCCTCGTCACCTTGGCGTTCGGCGCGAACTTGTCCGCGGATTGGCCGAGGACGAGCATCCGGGCCGAAGCCTGGCGGATGCTGTCCGCCGCCCAGAACAGCGGCGCGACGTCCGTGAACGTCCGCGTGCTCGCCGCGAAGTACACGCTGCCCGAGCCGGTCAGCCGCACGAGGGCGGCCGCGCCTCCCGCCGCCGGCTTCCACGGCAGCGGCGTCCAGCTGCCGTCCGCCGCGCGGAGCAGCACCGCCGTCACGTCCTTCGTCCGGACGCCCTCCGGCAGCGGCAGCGTCGCGCTTGGCGCCGGCTTCCAGCCTGCCGGCTCGAGGCCGAGCTGCAGCTTGGAGCCTGCGCCGCCTCCGAGCAGCTGGAAGCCTTGAGCCGCGGCCGCCGCATCCAGCAGCGTCCGCTCTCCGCTGTCGTTCAAGCCGAACGCCAGCACGAGATCGTCCTTGCCGCCGCGCAGCTGCGGCGCTCCGAGCGCGAGGCTCGCCATCGGCAGCTCGATGCGCAGCGTCTTGCCCGCCGCGGCGAGCTTGTCCGCGAGCGCCCGCTCCACCGTGACGCGGTAGCCTTCGGCTCCCGCCTCCGCCGAGCGGAGCGTCAGATCCGCCGCGACGCCGCCCTCCAGGACGGAGCCGTCCAGACGGATCAGCGCCGTCTTGCCTTCCCAGGCGGCTTCGATCGCCGCGCCGTTCACGCTCGCCTGCGGCTTGTCGCCCGCAGGCGCTCCGCCGCCTCCGCCGAAGCCGAAGCCGCCCGGCATCATCATCCAGATGCTCGCCGGCAGCAGCTTCGCCGCCATCGCCAGCTTGCCGCTGGACAGGCGCTTCGCCACGACGACGGTGTCGCCGTATTTCGCCGCGACGATGCCGTCCGCCGGCAGCAGGCTCCAGGTCGACAGGTCCTCCTGGAAGGCCGGCAGCTTCGCTCCCGCGCTATAGACGCGGTAAGCGAGCTGCTGCCCCGTCATGTCTCCGGCATCGGTCATGACGACGCGCGTCTTGTCCGTCGCGCCGAGCACCGCTTCTGCCTCGGCTCCGAGCGCGCCGAGCGAGGTCGGCTGCGGCAGCTTCGCCTCGGCGACCGCCATCGCTTGCAGCGTCATGCCGTCCGACACGCGGTACTCCGCCGTAATCAGGCTCGCGCCGGCGCCAAGCGCCGTCAGCGTGCCGTCCTCGGCGAGCAGCGCCGAGTCGCCGTCGACCGTCAAGGTCAGGCGCTCGCGCTCGGCCTCGGTCAGCGCGACTTCCTTATAGCGCGTCTTGCCGCTGCCGTCCTTGCCGTCCGCCACCTGGAGCACGGCCTGCAGCTTCACGCTGTCGCCCGGACGGAGCGTCGGGATCGGCTTCAGCACGATCGCGCTCGGGGCGCGGTAGCCGTCGTTCGTGACGTCCACGACGGCCGAGTTCTCATTGCCCGCCGCGTCGCGGGCGACGAACTTCAGCTCGGCCGACGCGCCGGCGTCCTCCGGCAGCAGCACCTCGCCGCCAAAGCGGCCGTCCTCCTCGACCTCGACCGGCTGTCCGGCGACCGTCAGCACGTCGCCCGGCGTCGTCGATCCGGCGACGCGCACCCGGCCGGCCTGCGTCCGCGCTCCCGTCGCCGGCTCGTCGATGTACAGCACCGGCGCGATCGTATCGACCGTCAGGTACAGCATCGTGACCGAGACGTCGCCCGTCGCCGTGTTGCGGGACCGCAGCTCGACGGCGAACGTGCCGTCCGTCGCGAAGCGGGTCAGCTTGAGCGAGCCGCGGCTGATGCCGCCCTCGCTGCGCATGTCCGCCTTGCCGAGGTATTCCTCCCCGACATAAGCCTCCACCTCGACGTTCGGCTGCGCCGAATGCAGCGAGATCGTCTGCTCGGTGCCGCTCGTCAGGTAGGTCCAGAAGGTTTTGCCCGGCTCGCTCGTCCTGACCGGACCGCCGCCGAGCGTCAGCTGCGGCTTCTGCACGAGCGGCAGCAGCGTCGCCGCCGTGTCGGCCCGATCCGCGTAATGCGGGTTGCGGTTCTTGTCGTCCGCTTCCGTCGGCACCGCCGAGGCGCTGACGCCGATGACGTACATGCGGCCGGTCTCGAGTCCGGCATGAGACACCTTCGGCGCCTCCTTGCCCTCCTCGCCGACCAGCTGCGTGCCGCCAAGTCCGGACGTATCGATCTGATCCGAAGCCGACACGGCCGCCCAGCCGCCGATCGGAATGCCCTCGTACTTGCCGCTCGCGGCGTTCCAGTACGGCTGCAGCTCCTCTTCGGTCATGAGCACGTCGCCGAACGGCTCGTACGCGATCCCGTTCTGGAAAGCCTCGACGACATAGCTGCGCTCATAAGCCTGCTGGCCGCTCTTGACCGCGCCGGGCTTGAACGACAGATGGAAATAGCCGTTGCCTGCCGGCTTCACCGCTACGTCGCTGACCTTGCCCGGAGCCATCGGATCCTTCAGCTCGAAGCGCTGCGCCGACGTCTTCGTGGCGAAGGCGTTTTCCGACTTGAGCTCCGCCCGCACATAATAGCTGCCTTGGCGCAGCAGGCCGCGGATGTCCTCCGTGCCGCCCGCCAGCTCGATGCGCCGGACGTCGATGCTCGCCCGTCCCGCCGCTGCCGGCAAGTCCTTGGCGATCAGCATGCCCGCGTCGCCGGCCTTGCGCACGACGTCGCCGCTTGCCAGCGTCTCGGTCGCGTCCGTTACGGCGTCCTTCGCCAAATACAGGCTCACCGTATCGCCCGGCTTGGCGTTATCGACCTTCCACGTCGCGGCGAACTTGTTCTCGTCCGCCGGATCCGCCGTCAGCCCGACCTCGCTCAGCTGCGGCGCCGTCGGCACGTTCAGCAGCTTCGTCTCGACCGGCGCCTGCGCGGTCAGCGTCCATGTGCCGCCTGCGGCCGCCTTGGCCGCCGGGATGATGACGTACGCCTTGCGCGAGTCGACGTCCGTCCCTGTGTTCTTCGCAGACACGACTTGCGTGAAGGCGTTGGCCGTCTTGTCGGTGTTCGTGTTGTCGAACTTGATCGGGTACGGCTTGCCGCTGCCGTCCTTCAGCGTGAAGGCCGGCATCTCCTTGCTGTCGTACTCCACCTCGATGATCGCGTTGCCGCTGACGCCGCCGAGCGGAATCTCATGCACGCGTCCGCCGTTCTTGACCGTAATGCCGCCGAGGCCGAGCGTCATGTCGCCGTTGTCGACGATCTTCATGCCGTTTCCGATCTCGCGGTACTCGATCGCCTGCGTCTCCTGCTCCGCCGCGACGCGGGAGTCGGCCAGCGCCTGCACGCCCGAGCCGATGACGAGCAGCCGCGGTCCGCGCTCCGGATCCTCGATGACCAGATGCGCGAGGCCCTCCGGCAGCTGGTCGGTCGACGTGCCGAACTCGACGCCTCCGCCCCAGTAGTAGGTGATGCCGAGGCTGATGAACAGGATGCCGACGCTGCCCCACAGCTTGTCGTTGTTGACGCCGAGGAACACGCTCGCCAGCGGCATGCCGCCGACGACCGGCACCGAGCCCGGAATCTGCACCTTGGAGCCGATGTAGCCCTCGAAGTCGGTGCGGTTCTTCTCCAGGTTCTGGCCGACAAAGATGCCGGCCTTGCCGACGATGATGTCCCAGCCGCCGATGTCGACCTCGGCTTGGACGCGCACGAACCACGGCGTCACCCACTGGGCTTCCAGCAGCGCCATCGTGATCATCTCGATGCGGTCGTCCTTTTCCGCGTTGGCGTCGGGGGAATAATCCATCACGCCCTCGATCTTGATGCCCGTCCGCTTGAGCGTCAGGTCGATGTCGCCGAAGAAGTACGCCGGCGCCATGCCGAAGCGCACGCCGACGCCCGCCTGGATCGTCAGCGGGAACGGATCCTCCGCCGTGCCGCCGGCGATCGTATCGGCCAGCTCGCGCACCGCGCCGCGGATCGCGGTCAGGTACGTCGCGCCGGTGATGAGGATGCCGGGGCTCTTGAGCTGCGTGCCGAAGGCGATCACATCCGGCAGGATGCGCCCGTCGTCGACCTGCTTGAGCGAGAACTCGATCGCGACCTCGGTCATGTTCTTGAGCTGCGCCTCGAATTCAAGGCCGTACGTGTTGCTGATGCCGTCCACCTTCTGGACGTAGTGGGTGACGCCGATGCTGCCGCTCGGCTTTTTCGGACCTTCCTCGCCCGACTTCTTGTCCTCCTTCGGCCCGAACAGGCCGAGGCTTTCGTTGAGGTCGAAGCCGAGCTTGGCGTCGATGCCGACGAAGCCCTTGTCGTTGAAGATGACGTTGTTGATCTCCGCGTTCACGATCTTCAGCGAGATCGAGCCGCCGAACGAGATGCCGCCCTCGCGCAGGATGAAGTCGTTCAGCGACAGCCCGAAGCCGTCGATCGAGAAGCTCGGAGCGCTGAACAGCGAGTGCTTGTTGAAGTACACGTTCTCCAGCATGATCTGGCGAAGCGGATTGAGCCGGTCGCCGACGCCGCCGACGGCCCATTTGAGGCTGCCGTTCTGGCTGTCGTCCTCCGGGTTCGTCGCCGACTGCTTGTTGGCGTCCTGGCTCTCTTCCTCCTCGTCCTCCTCCTCGTCCTCGCCGCTGCCGGCGCGCGGGATGCCGTAGCCGTCCCCGCCGAGCGTCTTGTCGAAGCCGTTGAAGAAGTCGAGCGTCCATTCGCCCTTGTGGAAAATGAAGCCGCTGCTGGCCACGCTCAGCGTGCCGTCGCCCTTGACGAACAGCGTGTCGAGCAGCGGCAGTCCCTCCGGCTGCTTGATGCCGAGGATGTCGAGCTTGCCGCGCACGAGCACGAGATCCTTGCCGCTGTAGGCGACCGCGCCGTTGATGATCGCCGGCTCGGTCTTCGTATCGACGATGATCTGCTGGTCGTCGCCGCTGCCGACCTGCTTGACCATGCCGCGCACAACGACGAGCGTCTCGCGCTCGATCTCATCCTCCTCGGCCTGCTCCTCGAACGCCTCCAGATCCTCTTCGCTCTCGAAGATCTGATAGTTGTAAAGCGGCGTCTCCGAGAGGGCGGCCTCGTCGGCGAACTCGCTCAGCTCGAATTCCGGATCGACCGCCTTGCTGGCCGCGCCGATCAGGGCGCGCGTCTTCTTGTACTGCGTCGCGGCCTCGTACAGGAAGCTGCCTTCCTCGAAAGGCTCGCCCGGGAACAGGCTGTTCAGCTGCTCCAGCCGCTCCTCGCCGACCGTCGCGCCGTTGTCGATGCCGCTCAGATCGACGACTTCCTTGTACAGCGCCAGGATGCCGGCCTCGCGGATGCGCGACTCGTCGTTGTCGGTGACGAGGATCGTCTGGCCCGACGCGATGTCGTACATCGAGGCGAGGTCCGGATCGTCGCCGGCCGTCCCCTTGTAGTCGATGACGATCTCGTACTCGCCGAGCGGCAGCTCGGGACCGAGTCCTTCCTCGATCACGCTGCCCGCCTCGTCGACCTTGTCGCCGCCGCGGTAGGTGATGCGCATGTCGCCGGTCAGGCCGTCGTCAGTCGGCTGCAGCAGCACCGAATCGGCGACCGGCACCCGGTAGCGCTCGCGGGTCGACTTCTCGACCAGGAACAGGTCGAAGTTCGGCTCCGTGCCGCCCCCGCCGGTCGTGTACGCCTCGATGTTGGACAGGTTGACCGTCATGTACTTGACGTCCGTGCGGTACAGCTCCTTGGGCGAGACGCCGTACACGTACGTCGGCGTCGCCTGGCCGACCGGCGGCAGCAGGATGAAGTTCGTCTTGACGGACTCGTACTGCGCCTGGATGCTCTCGTCGGCGATGCCCTCGATCTTGCTGCGCGTCTCCGGGCTGCGCGCCGTCAGCATGTACTGGCGGGTCGTCGGCCACGGCCGGCCTTTGGCCATCACCTTGAACGTCGCCGTCACCGTATCGCCGGGCTTGTACTTCGGCTGGATGCCGAGCTTAGCCTCCTCCGGCGTCGCCTCCTTGCGGTATTCGACGCGCTTGCTGCTCACGGTGTCGACGAGCGGCTTGCCGGAGCCGTCGCGCTTGATGTTCCCCTGCTCGTCGAGCTGCACGAAGCTCAGTCCGCTCTCGAGCGTCATCTCCAGCTCCAGGCGCGAATGCTCCATGTTGAACGACGGCAGGTTCTCGACCTCGGCGATGATGTCGAACACGCCTTCGTCGCGATAGCCGCTCGCGTCCGGCAGCGTGGCGAGCTGCTGAACCGGATCGACGTAGCGGATGGAGAACACTTTGTCCGGCGCGACGATCTCGCCGAGGCCGTAGATCGTCTCGAAGCTCTGCATGCGTCCCGGATCGATCGCATCCGGGTTCCAGTAGAACGCCACGGCGGAATCCGCGCTGCCGTAGTCGTTCGTGTCGCGAGTGAAGTCGAGGTTCGGATGGACCTCATAGTCCCACTTCGTGTTCGCCAGACCGTTCCAATGGCCGACGACCATCTCGTCGACGATGTTGATGTTCTGCTCGGCGACGTTGTTGAAGCCGTAGGCGACGACGTTCGTCGCCTGCGGATTCTCGAGGTGGAGCTTGTCGCGCATGACCCAGTAAGCGGGCAGCTTGTGCAGCGGCGCGTCTTCCGGAGGAATGCCGATCTTCTCCGGCTCATGCGTCAGCCGGCGCTCGACGAGCAGCGGCGCCTTGGACGCCGTGCCGACCTGGAACGCCGGGCCGTCGTTGCCGCCGACCATCGTATCGAGCAGGATCCGGCTGCCGACCTCCACCTTGGCGCCGCTGCCGTTCGTCACCTCGTAGCGGATGTTCACGTTGCCCGAGTTGATCTTGTCCTTGCCGTCCGTATAGAGCAGCAGGATCTGCTTGATCGACACGCCCTTCATCGACCAGACCATCTCCAGCTGCTTCGTGCCGTTCGGCTTCTCGACGAGCGTCGGCTCCGTCGTCCGCGACTGCTCGCTGCCGAACTTGTATTTGTTGCCGAAAATATAGTCCGTGCCGTCGATGCGGAACGTCGTGAACGACGTCTCCGGATCGTCTCCGCGGAACAGCAGGCTCACGTTCTGGTCCTGCTTGCGGATCGGCTGTCCCTCGATCGTGCGGATGCCGTACCGTCCCGTCTCGTTGTCGACCGTCACCTTGATATAGTCGTTCTGGATCGTCGTCGTCCGGCTCTTGCCCAGCTCGGCGGCCACCGCGTGGCCGCTCTCGAACAGGGCGGGAAATACGAGCACGAATGCCAGCAGCGACGACAGTCCGCGTTTAAGCAGCTTCACCGAACATCCCCCAGTTCCTTCGTTCATCACTCTATTTGACCGATCCGACAAAGAAGCTCGCATATTCGCGATCGCGCTCTTGCGTGCGGACGATGACCGTATACCAGCCCGCCTTCGGGAAGGTTACGGTGAAGCCGCTGCCTGCCAGCTGCTCGTACGTCAGCTTCGTCGCGATCGACTTCATCTGGCCTTCGCGGTACAGGCCCGGCTGGTACAGCAGCTCGAACGTGCCCGCTTCGTTGACCGCCGCCTTGCCGCCGACCTTCATGTCGCCGTAGCCGCTGACGCGGAACGTGATGCGGTTCGTATCGAACAGCGCCTGCTCGCCGGACGAGGCCGACAGCAGCGTGCCGTTGCCGAAGATGAGCAGCCCGCCGTTTTTGACGACGACGACGTCCTGGTACGCGACCGTGCGGTTGCCGACCTCGTCGGTCGCCGTGTAGGCGACGCGCTGGCGGCCGAGCTGGCCCAGGTCAAGGCCGCTGATCTCCACCTTGATCTTGTCCGCCGCCGACACATTGTCGGAAGCCTCGTAGCCGCCGAGATCGGCTGCCGCATTGAAGCCGGCCTTGTTCTGCACGATGCCGACGGAGCTCTGCTTCAGCCGCAGCGTCGGCGCGGCGTTGTCGAGGCCCGCTACTGTCACCGGAATCTGCGTGGCGTTGCCGAGCGCGTCGGAGATCGAGATCGAGGACACGCCGTTCGTCTCGAATATGCGAGAGTACGAGTAGGCTCCGCCGGCATCGCTCACCTGATTGCTGTAGGCGCCTGGCGTCCCGATCGGACGCAGGCCGGAGAAGACGGCGTTCGGCGCGGCGATCTTGCCGCTGACCGTCACCTTCATCCTGCCGGCGGCGTATTTCTTGCCGCCGATCGTGGCGATGCGGCTCGCCGGCAGCTCCGCGCCGTTCGCGTCGATGAACGTGTAGGACACGCGCTCCGGCTGCGGGCCTTCGCTGGCGATGCCGTCCACCTGCTCCTTGACGACGAGCGTATTGCCGAGCGCGTCGCCGACCGTGAACGAGACCACGCCGTTTTGCGTCACGGCGACGCCGTTGTTCTGGCTGTGCACGACGAAGTCGCGGGCCCCGGCGTCGGCCTTGACGACCGACAGCGTCACGCCCGAGGACAGCACGACGTTGCCGCTGCCGTCGGTGATCGTGCCGAACGTCAGGCTGCCGTCCTTGCCGTAGGCGTAGGAGCGCTCGATCTTGACGCGCGGCGGCGTGCGGTCGATGTTGGCCACGACGGCGGTCGCCTCGCCGGTGTTGCCGGCGGCGTCCTTGAAGGTGAAGGTGAAGCTGCCGTTGTCCGTGAACGTGTAGGCGCTCTTGCCGCCGTTGTTCGTGACGACGATCGGCTCGGTGCCGGTCAGCATCGCCGTCACGCTGCCGTTCGTCTGCACGTTGTTGCTGACCGAGTACTGGATGATGCCGGCCGGAGGCGTGCCGTCGACATGGTTCACGACGACAACGAGCGTCTCCTTGCGCTTCGCATCGTTCAGATCGCTCAGATCGAACGTGTAGAAGCCGTTCTCCTTGACGTTGAAGCGGTTGCCGGAGCGGACCGGCTGCACATGGTTGAGCTTCGACGGCACGATGCGGATGCCCGGCGGAGGCGCGATCTCGATCGTCGCTCCCGTCTGGGCGTTCACCGGCGTCAGCGACGGGATCGTCGCCACCGCATAGACCGGCTCGGCGTCGGGGTCGAAGCCCGCGGCGTCGACCGGATAGACGGCGCCGACCTTGCCGCCCGGCGAGCGGTACTTGACCTGCACCTGCAGCGCGGCCGGATCTCCCGACGGCACCTTCAGGCTGGCGAACGTCGTGTACGGACGCCATTTCAGCCAGGTCGATCCCCCGTCCGGGGACACCGAGTAGTCGTAGCCCGACGGATTTTCCGTCTGCAGCCCCAGCTTGACGATCGCCGTGTAGCCGTCCTCTTCGTCGCCGGTCAGGGAGATGAGCTTGGACGTGCCGGGAGCGGCCGGAGCGTCCTTGACCGGGCCGGCCAGCTTGAACGTGCCGGAGGTGGCCGCCAGCGCGGAGTTGCCTGCGCCGTCCACGGCCTTGACGTACAGGCGGAAGTCCGCCGTCTCGCCCGGCGCCAGCCGCTCCGCGCCATCCAGTTGCGCGACGCGGTCGCTCTTCAGCTCCTGCCAGCCGCCCGAGCCTTCCGTCGGCTCCGACTCCCCTTCGCGCACCCATTGGAACCAGGCGTTCAGGTTGTTCTTGCTGTACAGCTCCGCTACCGTGACGAGCACGCTCTGAATGGGCAGCGGATAGCTCAGCCCCTCGAGGCCGAAGCCGATCTGCGGCGGCTCGTTGTCGAAATAGTAGGCCCGGGAGTAATACTGCGTACGGTCGCCGAGCTGCGCCTTCACATGCACGTAGCGGACGCCGCTTTTCCCTTCATCCGGGATCGTATAGCTCGTCCAGCCAAGCTCGTCGGTGCCGAGCGGATCGAGCGGCGAGAACGCGCCGTCCGCAGGACGCAGCGGACTGTCCGACCAGGCGTAGCCGAGCGAATCCGGCAGCGCCTCGCCGATATGGAATGTCAGCTCCGAGCTGCGGACGAAGCTCACTTTCGGCTCCGGCAGGAATTTCGTCGGCACGGCCTGCTCCGAGCTCACCGTGATCGGCGCGCTCTGCGGCGTGTCGACGACGAAGTTGCCGGCTTGGTCCTCGGCTCTCAGGTAGAGCCAGTAGGCTCCGTCCTCGAACACGTCGCTGTAGGTCGACTGCGTCACCGTATAGGACGGCGCGTCATCGCCGTACACGGCGCCCGCCACCGTCGTCGCCGGCTTCCACTCCAGCTCCTGCGGATCGAAGCCCTCCTTGACCCACTGGTAGCCGATGCTGCGGATGCCGCTATGCGGCTCCTCGACGAGCGCCTCGACCGTCACGTTGGCCGTGCCGTCTGCCGAGACGGCTGCCGGCTGCAGCACCGGCTGCTTGTTGTCCAGGCGCAGGATGCCGACCTCATGCGTCCAGTTGGAGTCGTCGTGCTTGAAGTCCTCCAGCTCCCAGAGCTTGGAGTCGCCGTACTGGCCGACCGCCTGCAGCGCCTTGTTGTCGGCGTAGACGGTCTTGTCCGCCTCCGACTCGCCCGGCGCCTCGGCCTTCCATGCCTCGTACTGCTGCGGATGTTGGGCGACGTAGTCCTTGCTCTTGTCGTACTGCATCAGCTCGCGGGCGGTATCCCACGTCATGTCCGCCGTCCACGCATGCAGGTACCACTTGCCGCTGTTCTCCGGCAGCAGCGCCTCGGGCGGCGGCGCGATCAGGTTCGTCTTGTTGTTCGTCACCGACAGCGTGAGGCCGGCCATCTCCGGATACAGCTCCTCCGCAGGCTGCTTGGCCGACAGCGAGTAGCGCTTGATCGCGGCGAAATGGTCGCTTTCCTTGCCCGCGAGCGGATCGGCCGGCGACTGGCTCCACGTGTAATAAACGAGGCCGATCGACGGCGACGCCTCGGCGCTCATGTTGCTCGGCCGGTAGATGCCGCGGCTCGGACGCTCCAGCCCGCGGTCAGGGACGGACGGATCGAGCGGAGGCACGAGCAGGGACGGATCGTTGGCGTCGATCGTCATCTTGCCTTCCTTGGCGTAGGTCGAGCCCGTAGCTCCGCCCTGCTCGTAGCGGTAGCCGATGATCGGCTTCGTATTGTCGATCATGAGATTGGCCCAGTCGATCTTGGAGCTTACGAGCGACGGCTCCAGATCAAGCGGCGCATTGGCATAGGTATCCTGGAAATTCGCCGGCTGGATGAGCAGGTTGCCCGCATAGTCCTGGATGACCTCGAGATCGGATGTCTGCGGCGTCTTGCGGTCATGGGACAGCGAGACGACCTTGAGCAGCGGCGTCTCGAGGTCCACGGAATCGCCGATCGTCGCCCGGAATTTCCATACCGACTTGCTGTAGCCGGAGACGTAGTAGGCGCGCATGCCGTTGTTGAACAGCAGGTACGTGCCGTTCTCCTGCCCTTCCCACAGCCGATTGACGATACCCGGCTCGGTGAGCTGCACGCTGAAGTCGATGACGTCGCCTTTGTTCAGCGTCGTGCCGGTCAGAATTTCCGGCTGGATGCCGTTTCCGCTTTTCGTGTACTTCGGACGCACCGCGTCGACGATGACGCGGTAGCCGCCGGATTTGTAGTCGAACGGATCGACGGCGCGGCCGGCAGAGACGACGACCGGCAGGCTCCCCGCGCTCGCCTTGTTGGGGAAGCGCATCGAGGCGACGTTGCCGGCGGCGTCCGCCAGCACGGCCTGCTCGAGCTTCTCCTTGAGCGAGAGGTCCATCGGCAGCGCGTTCAGCGTGCTCGTGTCGACCCTCGGCTCAAGCGGCAGGTTGCCGCTGTTGTGGTACGCCGAGGCGACGTAGCGATAGGCGAGCCGGTCGTGGTAGGTGCCGAGGTTGGCCGCGCTGTAGGTCGTGTTCTGCAGGTACTGCTGCTGGCCCTCCGCCGGCAAGCCGGTATTGGCCTGGTTGACGAACAGCGGATGCCTCAGGAAGTAGTCCGAGAAGCCCGCCGATACGGCGGTCGGCCGGATTGGCTCGCTGAAGTTGTAGGCGAGGTCGACGAACTCGTTCTTCTTGACGTAGAGCTCGGTCTGGTTGATCTCGGTGTTCAAGCGCGTCGCGCCGTTGCCGGTGAACGTATAGTCCTCCAGCACGGGACGCTGCTTGTCCTCGAACAGGATGTACAGGCCGCGCACGCCGGTCGGGCCGTTGTCGTCATCCTCGCCGGAGACGCGGATCCTGATGACCGCGCCCGGCGTCAGCGTCTCTTGCTCCGACTTGTTGTAGATCTGCGTGCTTCCGCTCGTGTCGTCCGTATCGTAGTCCATCAGTTGCCGGCCATTGACCGTCACGGTGATGCTGGAATTCTCCGTGCCCGAGAAGACGCCATAATGCTTACGCAGCACGGCGAAGCCGATCTTGAACGTCGCATGGCCGCTCTGGGCCATCGCCGACAGCAGAGGGTTCTCTCCTACGCGCAGCGTATAGGTCGCGCCCGAATTGACCGTGAAGACGTCGCCCGCGCCCCAGTCGGCCGACGTAGCCGAATCATGCTCCATGTAGAAGCCGCTTTCCATGTTGTTGTAAAAGTTGCCGAACGCGTTCTCAGCCCCGTAGCTGAGGTTTCCGATCCGGTTGCCGAACTTCTGCTTGACCTCGATGTCCGCCGCGGCCGCCTCGGCCGGCTTCACCCAGCCTCCGGACGCCGCTCCCGCGAGCAGGCTCGCCGCCAGCAGCAGCCCAAGTCCCCGCTTGCCTTTTTTGCGCAGCAACACATTGTTGCCCCCCTTATCCCCTTGTCGAACTGAGACGAACGTCCCGATGATTCGACATATTCTGAGACGATTCTAAGAAAAGGGAATAAACGAAAAATAAACAGCCGATAAACAAGCGCAAAAAGAGAGGGTGTCCCGACAGCCTTGGCTTAGGGACACCCTCTTCTAAATGGGTTAACACAAAAAAACTTCCTCTTCCGGGAGGAGTAGACGCCGGCCGGGAAGCGGGCCATCCAAGGCAGAATTGTGCCTTGGATTCGGCTCGCCGGCCGGGAGCCGGGCCATCCAAGGCAGAATTGTGCCTTGGTTCCGGCTCTCCGGCCGGGAACCGGGCCATCCAAGGCAGAATTGTGCCTTGGTTCCGGCCCTCCGGACGGGAGCCGGGCCATCCAAGGCAGAATTGTGCCTTGGTTTCGGCTCTCCGGCCGGGAACCGGGCCATCCAAGGCAGAATTGTGCCTTGGATTCGATTCGCCGGAAACCAGCCTGCACGGAAGCGGAAGGAAACCGAGAAATCAGCGTCAGCCCGCAGTACATGATGCCAAAGAAGAAGGAGCGCGATAAACTCTCCCGTGAAGAAGGACACGCCCTTTCCGTCCGGAGGATTCATGAGCCGGAAAGTGTGTTTGGACAACTGAAAAACAACCGGGGGTTCCGGGGGTTCCGGGGGTTCCTGCTTCGCGGCTTACTAAAAGTAGGCTTGGAGGCCGGGGCGCTTTCCCTTGCCCGCATTCTACTGAAGAAAGCCAGCTGTGTATGCACAAAAACCCCGAATGGAAATGGAGCCGAGGCAACTGGCTTCATGCTTCATCCGAGGTCTTTGCTGTTTTTTGAGATTTTGGGATGTCTCCATTTGCTTTCGGGACAGCCCCTTTTTTGAAGGATTAGAAATGGGCGGAGCCGACGTAGGAGGCGAAGGGGCGGGCGGGAGCAGTGCCCAGCTCGCGGGCGAGCCGCTCCTCCAGCTCCCGGTACTGCCTGGCCGCGTCATGCGTGCGGCCGAGAAACAGATAATGCCGGATCAGCTCCTCGTGGATGTCCTCGCGCAGCGGATCGAGCTCGAGCATCTGCTCGAACAGCGGAAACGCCGCCGCCGGCTTGCCGTCCCGCACGAGCAGCCGCGCCTTGCCCTCCAGCCGCTCCATGCGCTCCCGCTCCAGCCGCCGGGACAGCTCCGCCGCCCATTCGTACAGCCTGCCCTGAAGGAAGCCGCCCGGAGCCGCGGCCTCCGCCTGATCGAACTGCCGCGCGTCCGGCGCCGCCTCGGCGCGGATGCGCTGGACGAGCCGCTCGTACTCGTACAGGTCGCAGTCGACCCTCGCGGCGTCGATGCGGATGTCGTAGCGCCCGGCCAGCAGCAGCGGCTCCAGCCCGGCCTCGGCCAGCGACTTGCGGATGTAGTAGAGCGTCGAGTTGATGTTCTTGGCCGCCTTGTCCGGCTCGAGCCCGCGCCAGAGCGTGTCAGCGACCTCCTCCCGGCTCGCCGTCCCCTTGCACAGCAGATAGGCGAACAGCTCCTCGGTCTTCGGGCTGCGCAGCTTGATCGGCGTCTCGCGTCCGGGGCCGTCCGTGCGGAAGAAGCGGAGGCCGCCGAACATCCGCACGCCGAGCTTCGGCGCCGACGGAGGCGGCTGGGGCGGACGCGCGCGCCGGCTCAGCCGCTCGAGCGTCTTGGCGAGCCGCTCCGCGTTGACCGGCTTGAGCACATAATCCACCGCGTCCTGCTCGAAGGCGTCGACCGCATAGCGGTCATACCCGCTGACAAAGACGATCTGCAGCGGCTCCCGCAGCTGCCTCAGCCGCAGCCCGAGCTCCATGCCGTCGATCTCCGGCATGTTGATGTCGAGGAACGCCACGTCGACGTGATGATCCCGGACGTAGGCGCAGGCCTCGGACGGATGGAAAAAGGTCGCGGCGATCTCCACGCCCCCCAGCTCGCCGGCGATTCTCGCCAGCCTGCGCATCGACAGCTCCTCGTCGTCCACGATGATCGCTCTCAGCATCGGTCATCCTCCTTCTTTCGGTTCGCTCGTCCGGCTCGACGCCGGGATGCGGAACGTCAGCCGCGAGCCGAAGCCCGTGCGGCTGTCCATGCCGAGCCGCTCCCCGTACAGCAGCCGCAGCCGCTCGCTCACGTTCCACAAGCCGACGCCGCCGATGCGCTCCGGCTGCTCGAGCCGGAACAGCATCGCCTGCGCGTCGAAGCCGGCTCCGTCGTCCTCCACCGCCGCATGCACATAGCCTTCGCGCTCGACCACCGTCACCTTCACCTCGCCGCCCTGCGGCCTCGACAGCAGGCCGTGCCGGATCGCGTTCTCCACGAGCGGCTGCAGCAGCAGCGGCGGAAACCGCAGCGCCGGATCGGCCTCGCAGCGCAGCGTCACCTGGAGCCGCGAGCCGAAGCGGGCCTTCTCGATCTCGGTATACGCCTCGATCAGCCTCAGCTCCGCGCCGAGCGTCGACATGCCGTCCCGCTGACCGAAGTCGAAGCTGCCCCGCAGATAGCCCGACAGATGGAGCGTCAGCCGCTCCGCCTTTTCCGGCTCCTCCACGCATAGCTCGGCGATCGCCCCGAGCGCGTTGTAGAGGAAGTGAGGGTTGATCTGGGAGCGCAGGAAGGCGATTTCCCGCTCTCGCGCCTCGCGGACGGACTGCCGCAGCTTGACGAGGCTGCGGACTCGCGCCAGCAGCTCCTCCGCCTCGAACGGCTTGGAGATGTAGTCGTTGGCGCCTAGGTCGAGAGCGAGCCTGCGCTCCTCCTCGCGCCTGCGCCCGGTCAGCATGAGCACCGGCAGCTCAGAGGGCGAGAAGCGGTTCCGCAGCTGCTCGAGCGCATCGAAGCCGCTGCCGTCCGCGAGCGAGACGCCAAGCAGCACGAGGCTCAGCTCCCCCTCCAGCGCAAGCGCCGCGCGCGCCTGCTCCGCGGAGCGGACGCTCACGGCCCGCAGCCCTTCCTGGGCAAGCAGCTGGCACACCGCATGCCGGCTGGCAGCGTCCGGCTCGGCGACGAGCACGACCGTCTGGCCCTTGCTGCCGCCGGCAAGGGCGACAGGCGTTTCGGAGGCCGCCGCCGCCTCCCCTGCGGCCGGCCAGGCGGCCTTGCGGGAAGCGGCGGGATTTTTCTCCAGCAGCAGGGAGAAGCGGAAGGAGCGTCCTTCCTTGCCCGGCAGCGGCTGAAGCGCCAGTCCGCCCTGCAGCTCGATCAGCCGGCGCGTGATCGACAGCGCGAGATCGGCAGCCTCCCCGTCTGCGGCGGCGAGGCATGGCGCGACATCCGGATCCGGAGCGGGCCTCGGCCGGCCGTCGAAATCGACGGTCACGACCGCGAAGCCGAGCTCCTCCTCGGCCGTCACCTCGATCCGGCCTTCTTCCGCCCGCAGCGCCGCCCGCTCGACCAGCCGGTGCAGAATCTGCTCGAGCCGATCCTCGTCCGCATAAACAGCCGCCAGCGTTTCCGGCACTCCGTTCGCCAGCTCGATCGGCCTGCCGCTCAGCAGGAAGCGATGCAGCTCCAGCACCGAGCCGACCGCGGAGCGGAGATCGAGGTTGCGCGGCTCCGGCACGATGTCCTCATGCTTGAGGCGGGAGAAGTCATGCAGATCCTGCACGAGATAGCCGAGACGGCGGCCCGTGCCGGCGATCAGCGCAAGGCTGCGCGCGGAGCCGGGAGCAGGCCCGCCGGCATGCGCCAGGCTGTCCGCCAGATGCACGATGTCCTGCAGCGGAGCTTTGAGCTGGTAGGTCGTCGACGAGAGGAACTCGTCCTTTTGCCGATCGAGCCGCAGCAGCTTGCGATGCATGCGCTCCATGTCGCGGAACGCCCCGTAGAAGCGGTAGACGATGACGAGAAACACGACGAGGCTGAACAGAATCAGATAGATCTGGCTGATCAGCAGGGAGCCCAGCATCGACATGCCGAACAGCAGGCAGCCGTAGGAATACAGGTTGAGCAGCAGCACGGCGAGCAGCAGCAGCAGCGACTCGTAGCGCTGGCCGCGAGGAGCGGCGACATGCCGCGCCGCAGCGCTCCACAGCACCCGGGCCATCAGCACATGCTCGAGCAGGATCGTGACGCGGTACAAGGAGAGGTACTCGCGGATGCTGAGGAACGGGAACATCACCAGGCTGCCCAGCAGCAGGAGCGCGAACAGCTTCGTCAGCCGCCGGTCCGCCCCTTTCCCTTGGAGCAGCATCATCAGGTAGAGCGAGACGAGAAAGCCGGCCAGCGCGCTCATGTCCTTGATCGTATACAGCGTCTGGAAGGAAAGCCCGTCCAGCAGCAGGGCAAGCGGCCGCTCTCCGAGCAAGCCGTTGAAGACGGCCATCGTCACGCAGGTGAGGCCGAACAGCAGCAGCGGCTCGTCGCGCTGTCCGTACAGCCATACCGCCGCGAACAGCACGAGATGGATGAGCCCGATGACCGCCAGCACGACCGCCATCGCCGACTCGCGGATCAGGCTGCGCTCATGGGCTGCGTTGATCGCCTCCTCCTTGCCGAAATAGAGCGACATCGGCACGCCCGCATCGATATAATCGTAATTGGCCGCGTGCACGATGATCTCCGCCTCCGAGCCCTTGATCTCGACGACCGCCAGGCCGGGAGAATTGCCCGGAACGTAAGCTTCCGCCGAAAGGGCGGGCTTGCCGTCCTCGAGCACGAGCCGGCCGTCGACGTAGATCGCGCTGGCGAAGCGGATGTTCATCTTTTTGATCCTGTACACGCCCGGCTCGGACAGATGGGTCAGGCGCAGCCGATAGGTGGCCGCTCCGTAGACGGGCCGCTCCGCGCCTGCAGCCCGGCTGCCGCTCCATACGCCCGGCACCTCCATCCACGAGCGCTCTCCCCGCGGCGTCTCGCCCGGCTGCAGCAGCTCGTTCCAATAAAACTCCCATTCCCCGTCCAGCGCGATCCGGCCGGAGCCGTCCCAGCCCGCCAGATCGATCACGCCTTGCTCCGCCCGGAATGGCTGCTGTCCGCCCCATCGCTCCGAAAAGATGCCGAGCGGCAGCCAGATGCCGAACAGCACGACGATCCCCACGACGCCCAACCCCTTACGCCACAACCGTTCCGCCCCCACCCACTACTTACATATCAATATTTCCAGGTCTTATTTATCGGCTTCAACGAGGCAATCGTGAAGAGGCGGAGGACAATCGCTTGGCGGCTCCGCGTCTTCGCTGCTGGTACAAAGCGTCCCGTCCTTCTTGGATCGCGCCTAGAACCACGAGATAGATGTCCTCATATGATGAATTAATTCGCTTCATTCACCTAGACCTGCCATGCGTTACCCTTCGTTCCGGAAGGAGATTCACCGATGCTCAAATCCAAGTCCAAGATCGCCGTCCAGGTGACCCAAGGAGGCCACGGAGCCGACGATGCGATCGTGCTCGGCGAGTCCGTCCTCAAGCATCACAAGATTCCGTCCGGCACTCCGATCGCGCTCCGGTTCGGCTCGTACCGCACCGCCGTGCGGGTCGTATCCGGCGGCAAGGGCGACACGATGCGGCTGCCCTCCGCGCTGGCCCGCAGCCTGGGCATCCACGGAGCCGTCTCGCTGCGGCTGCACTTCCGGCCGAGCACCCAGACGCTGTCGCTCGGCCCGCTGATCGGCGTGCTCGTCAGCCGCGACTATCCGCAGCAGCCCGATCGGCCCTTCGGCTCGATCACGATGTTCTGCCGCGAGCTGGTCGACGCCTGCGCCGCGCAAGGCGCCCATGTATACTTCTTTACGCCCGAGGCGGCCGGTCCCGGTCCGCGCATCGACGGCTGGGTGCATGGCGACGGCGGCTGGCGCAAGGCGAGCCTGCCCGTGCCCGACGTCGTGAACAATCGGCTGACGGCGCGCAAGCTCGAGAACCGTCCGTCCGTCCAGCAGCTGTTCAGGGAAGCCAAGTCCCGCTACGGCACGCAAGTGTTCAACGAAAAGTTCCTCGACAAGCATGAGGTGTTCGATGCGCTCGGCAAGGACCCCTCGCTCGGCAAATACTTGCCGGAGTCGCGGCTGCTGAAGAGCTTCGCCGATCTCAAGACGGTCTCTTCCCGCCACGCTACCGTCTTCCTCAAGCCGGTGCGGGGCAGCCTCGGCAAAGGCATCATCAAGGCGAGCCGGATGGAGGGCGAGGGCATCCTCGCCACCTACACCGCCCCGACCGGCATCCGGCGGCAGGCGTATCCGACTCTCGCCAAGTTCTACGGCTCGCTCGGCGGCAAGATGAAGACGGTCCGCTACCAGCTCCAGCAAGGCCTGACGCTGATCGACATCGGCAAGCGGCCGGTCGACTTCCGAGCGCTCGTGCAGCGCAGCGGCACCGGCGCCTGGATCGTCACATCGGTCGTCGCCCGCACGGCCGGCAGCAATCACTTCGTCTCCAACCTGGCTCGCGGAGGCACGCTCAGCCGCGTCAAGGACGCGGTCGGGCGCAGCAGCCTCGCTCCCGGCTACAAGGCCGGCGCAAGCGCCAAGCTGGAGAAGGCCGCGCTCGACATCGCGAAGGGGATCGAGGAGCGCATTCCCGCCCACTTCGGCGAGCTCGGCATCGACCTGGCGATGGATACCGGCGGCCGCGTCTGGCTGCTGGAGGTCAATTCCAAGCCGTCCAAAAACGACAACACGCCGCTCGAAGGGGGCAAGATCCGCCCCTCGGTGCGGAACATGATCCAATACGCGCGTTACTTGGCCGGCTTCCAATAGCGTCCGGCCCGCCAGCCCGCCGCCGGTCCGCCGGCAGCAGCAGCTGAACCCCGTGAGGAGGAGCCCGCGATGAAAAGCGATGCAGGCGTAATCGGAGTATGGATCGGAAAGGCGCCCCGACCGGACGGCTCCGGCAGGCTGACGGTTCCCGAGGACGGATTCCTCGCGGCTCTGGCCGAACGGGCCGCCGAGCTGCGCCTGCCGCTGCATCTGTTCGCCGCGGAAGGCTTCCGCGCCGAAACGGGCTCCCTGACCGGCTACGTCCGCGAAGGCGGATGCTGGCAGGAGCGGGAAGTCGCGCTGCCGGCCGTCGTCTACGACCGCTGCGGACCGAGCGGAGCGTCCAGCCGTCGCTCCAGCGAGCTGCAGCTGGAGCGGATGCGCCGCCTCCATCCTCATGCGCGGCTCAGCAGCTGGCTGCCCGGCAAGCTCGCGCAGCTGGAGGCGCTGCGCCGCGCCGGCTCCGAGCTGGCCGCGCTCGCGCCGCCGACCCGCCTGCTGAACGGGGCATCCTCCGTCGCGGAGGCCGCGCGCGAATGGGGAGCGGTCTTCCTCAAGCCGGACGGCGGCATGCAGGGACGCGGCGTCCTCTCCCTCGGTCCGGACGGCAGCGGCTGGCTGCTGCGCGGCCGCGCCGGGGACGGCCGGACGCTGGCCGCCCGCTTGCCCGACCTGGAGGCGGCGGCCGAGCGGACGGAGCGGCTGGTCCGCGGACGCCGCTACATCCTCCAGCCGCAGCTGCCGCTATGCGACCGCCAAGGCCGGCCGTTCGACGTGCGGGCGCTCGTGCAGAAGGACGGGCGCGGACGCTGGCGTCTGACCGGCACGGCGCTGCGGCGCGGCCGTCCCGGCGGCATCGCCTCCAACCTGCACGGCGGCGGCGAGGCGCTGCCCGCCCGCGACGGCCTCGAGCTGCTGCTCGGCGCCGAAGGGGCGGCCCGCTGCTCGGCCGAGATCGACCGGCTGGCGCTGCTTGCCGCCGAAGCGGCCGAGAACGCCTTCGGCCGGCTCGCCGAGCTCGGCCTCGACTTCGGCGTCGAGCCGGACGGCCGCCTCTGGCTGCTGGAGCTCAACTCCCGTCCCGGCCGCGACGCCTTCTCGTCTTTTCCCGGCGGCATCGCCCGTACGGCGGTGGAACGCCCGCTGCTCTACGCCCGCCTGCTGGGCGCGCGCCCTGTCCCGGAGCGTTCCGGCGCCCGATCGTCGGCCGCTCCTTCGCGATAAATCGACCCAACCTAGCGACAGAACGTTCAGGAGGTTCATCATGAGTCTTACTTTGTGCAACGTGCATTTTTCGGATAAGAAGGACCGTGTCGTCTATGTATCCGGGCCGCTGTACCGATCGCTCAAGCTGTCGGACAAAAAGAAGCTGCAGATCAAGCTCGGCCGGGAGACGGTCACCGCCTCGGTCAAGGCGGTCAAGCGCGAGGGCAATCATGTGTTTCTCAGCTCGGCGCTCCGCCAGCAGATCCGCGTGCCGAAGTCGGGCAACGTGTTCATGCTGCACGCCTCGGAGAACGAGGTGCAGCTCGGGCCGCTCGTCGGTATCCTGAGCGACGGTTATGTCAGCTCCTCCCTGCCGTTCGGCTCGCGCACGGGCTTCATCAAGGACCTGATCCGCATCGGCGAGAAGAAGGCGTATTTCTTCGGCTTCACCCCCAAGGACATCAACTGGCCGCAGGAGACGGTGAACGGCTATTTCCTGAACGCCGACGGCTCCTGGTATCGCAAGACCGTGCCCCTCCCCGACGTCGTCTACAACCGGCTGCCGAGCCGCAAGGCCGAGACCGGTTCCTATATCAGCTCGCTGCGCGAGCGCTTCGTCCGCAAGGGCATCCCGTTCTTCAACTGGAGCTACTTCAACAAGTCCGACGTCTACAAGCTGCTCGACAAGGACGTGGAGGCGCTGCGCCATCTGCCGGAATCCGTCTCCGGTCCGAGCGACGCCAAGATCAAGGAGCTGCTGGAAAAGCATCACTTCGTCTACTTCAAGCCGAGCGGCGGCAGCCTCGGCGCCGGCATCTACCGGCTGACGTACCAGCCGAAGCAAGGCTACTTCGCCCGCTACCGCAGCGGCGGCAAAAACGTGCTGCTGCGCTTCGGCACCTTCCAGGCGCTCATGCGCACGATGCACGCGCGGCACGGCAGCTCGTTCGGCGGCTATGTCGTGCAGCAGGGCATCCGGCTCGTCGAGATCGAGGGCTGCCCGCTCGATTTCCGCTTCCACATGCACAAGAACGGCCGCAACGAATGGGTGACGGCGGGCATCGGAGCGAAAAAAGCCGGCAAGGGCAGCGTGACGACGCATATCAAGAACGGCGGCGTGCTCATGACGCCGGGCAACGCGCTCTCGCGCACGTTCGGCAGCCAAGCCGGCGAGGTGCTGGAGAAGGCGAAGCGCGTCGCGGTCCGGATGAGCGAGGCGATCGAGCGCAACTACCCGCATCGGCTCGGCGAGCTCGGCCTCGACCTCGGCATCGACAAGGACGGCGAGGTGTGGATGTTCGAAGCCAACGCCAAGCCCGGCCGCTCGATCTTCAAGCATCCGGCGCTCAAGCCGGAGGGCCGCGCCTCGCTGGAGTACATCCTCGAGCACTGCCTCTACCTGAGCCGCTTCCGGGGGAGGGACAGCTGATGGAATACGAGCTTCCGTACGGATTTTCAGCCGAGCTGACCGCGCGCAAGCCTGTGCTGGCGATATTGACGATGTCCGATCCGAAGCTCGGCTTCCGCGGCAACCGGGCCAATTTCGCCGATCTGGTCCGGACCGGCAAGGAGATGGGCTTCATCGTCTACGTGCTGCCGATGCGCTACCTGAAGTTCTCCCAGCCGATGCTGACCGGCTTCTCGCTCGCCGACTCGGCGGGCAAGGGCGGCGAGTGGGAAAAGGGACTGTTCCCTTTCCCCGACCTCGTCTACAACCGCATCCCGCAGCGCGAGGATGAGCTCATGCCGCGCGTCCAGCGCAAGCTGAAGCTGCTGCTCGCGAGTCCCCGCGTGAAGGGCGTGTTCAACCCGTCCTTTTTCAACAAATGGGAGCTGTTCGAATGGCTGCGGAAATCGCAGGCGACGAAGCGCTACATCCCGGCGACGCGCCGGATGGCGACCGTGGGCGGACTCGACCGGATGATGAGCAAGCATCCGTACCTGTACCTCAAGCCCGTCAGCGGCAAGGCCGGCAAGGGCATCATGACGATCCGCGTCTATCCGGAGAAGCCGCTGCCGTACCGGCTCAGCATCCAGAACCGGAAAAAAAGCAGCACCTATAATTGTTCGACGGTAACCAAGCTATGGGCGCGTATCCTGAAAGAGAGCGGCGGCGCAACGTACATCGCCCAGCAAGGGATCGACCTCGCCTTGTACCAGGAGCGGCGGTTCGACCTGCGCGCGCTCGTGCAAAAGAACGGCGCCGGCCAGTGGTCGGTCACCGGAGTCGGCGCGAGGGTCGCCGGCTCCAAGAGCATCACGACCCATGTGCCGCGCGGCGGCAGCATCGAGGATCCGGAGAAGCTGCTCAGCCATGCGTTCGGCGCGGAGAAGGCGCGCCAGCTGATCAGCCGTGCGCGCAGCGCCTGCGTGCAGCTGGCCCGTCAGATCGAGTCGGCCAGCGGCCATAGCCACGGCGAGATGTCGATGGATCTCGGCGTCGATGCCGCGGGCGGACTGTGGTTCTTCGAAGCCAACTCCAAGCCGATGAAGTTCGACGAGCCTCATATCCGCAAGAAATCGCTCGAGCGCATCTTCCATTACGGCAGCTATCTGATGCGCTCGCCGAAGCCGGGAAAGGCTGGAGGCGCTTGACATGAAGGCAATGCTTCTGACACCGAAGCAATGGACCCGCAGCCGGGAGCCGCTCCTGCGGCTGATGGCCGCCTGGGGCGGCGGACGGCTGTCGGCGGCGGGCCTCGCGGCTCTGAAGGAGCTGCGGGCGGAGGAGCTGGAGCCCGCGGGCGGAGGGGCTCCGGCGGCGGCGCTGGCCGTCCTGCTGGAGCAGGGACGTCCGGCGGGCATCGCCTTTGCCCGCAAGGCAGGCCGGGAGGCCTGCCTTGTCGCCGTCTCGCCGCCCTGCCGCGGCCGAGGAGCCGGCAGCCGGCTGCTGCGCGAGCTGCAGCGGACGTGGGGAGCGCTCGACTGCCGCGTCGCCGCGGACAACGCCGCGAGCATGAAGATGTGCTTCCGCGCCGGCATGGCCGCAGTGGCGCTGGAGGATGGCCCGACCGGCAAGCCGACGCTCGTGTTCCGCAGCGGCGCCAGCGCGCTTGCCGCGCAAGGCGCGCAAGACGGCGCGGCGCGGGCGGAGGCGCTCCGCGAGGCGGGGCGGATTGAGACGGCGCAAGTCAATGCGGCGCGTTCCCAGGCGGGGCGGTCTGAGGTAGAGCGTTTCGAAGTGGAGCGGCCTCAGGCGGAGCGGTTCGAGACGGCTTGGTTCGAGGCGGCTCAGCCTCAGGCGGAGCGGTCCCAGGTGGGGCGGTCCGAGGCGGAGCGGTCCGAGGCGGCTTGGCCTCAGGCGGAAAGGTCCCAGGTGGGGCGGTCCCAGGTGGGGCGGTCCCAGGTAGGGCGGTCCGAGGCGGGGGCGACGAGAGCAGCGCGCACCGCAGGCGCGGCGCGAACCCCCTCCTCCCGGCCTTCCGGCCGCGAGCTCCTTCCGAAAAAGCCCGCTGCTGCAAGGAGGGATGATCATGGCTCAGCCGGTGCTCGGCATCTTAACGTTATACCTCAATGAGAACAAGGCGCTCGAGGAGCGCCCGATCTATCAGCGGATGATCGTCGCCGGCAAGAAAATGGGGCTCGACGTGTTCGTCTTCACGCCTGCCGACGTCGATTACGAGAAGAACCGGATCCAGGCGATGATCTACGATCCGTCGTCGAAGACGTGGTCGCGGCGCTGGACCTCCTTTCCCCATATGATCTTCGACCGCTGCCGCATCCAGCAGAGCTACCGCTTCGAGCAGCTTCAGAAATTCCGCTCCCGCTACGGCCATCTGACCTTCCTCAACCGGATGCTGCGCAACAAATGGACGGTGTACAAGACGCTGGCCGCGCAAAGCCGGTTTCAAGGACGGCAGCCGCTGACCGTGCTGTATGCCGGACACAAGGATCTGGCCGACATGCTGCGCCGCTTCCCGCTCGTCTTCCTCAAGCCGATCAACGGAACGGGCGGGCGCGGCATCCTGCGGATCGAGCGGCAGAAGGAAGGCGTCTATCTCATCCAAGGACGCGATCAGTCTCGGCGCATCATCCGGCCGCAGAAGGTCGGAGCGGCCGCGCTGCAGGAGCGGCTTTCCTCCTGGAGCCTCGGCGGCGGCAAGTACATCGTGCAGCAGGGCATCATGATCAAGCTGCCGAGCGGCCGCGTCCACGACTACCGGCTGCTCGTGCAGAAGAACGGCCGCGGCGAATGGGAGCCGACCGGCTGCGCGGGCCGGGTCGGCGCGGCGGGCAGCATCACCTCCAACCTGCACGGCGGCGGCAAGGCGATGCGCATGGAGGAGCTGCTCTCCTCCTGGGTCGGCGACGAGGAGCTGGCCGCGTCCGTACGCCGCGAGGCGGAGCAGTTCGGCGTCGAAGTCGCGGCCCATCTGGAGCGGCAGTACGGCCGCCTGTGCGAGCTGGCGCTCGACCTGGCGATCGACAAGAAAGGCGGCATCTGGCTGCTCGAGGTCAATCCGAAGCCCGCGCGCGAGGTGTTCCGCCAGAGCGGCGATCTCGCGACCTATGAGCGGGCCATCGTGAAGCCGCTGGAGTACGCGCTGTACCTCTACTCGAGACGCGGACGCAAGTCCGGCGGCCGCACGACAGGCGGCCGCACGGCCGGGTCGCGCACGAGAGGCTCGCGCACGGCCGGATCGAGGACGACGGGCTCGCGCACGACCGGTTCAAGCCTGGGCGGCGCGCAGCCGGTCGGCTCGGGGCCGGCGGCAGACGAAGCGGCGACGCTCGGCTCCGGCTCGAAGCGCCGGAATGCGGAGCCCGGCGGCAGTCGCAGCCCGGCCGGGACGGCCGCAGGCAGCGGCAGGAGCGGATTGGCCGGATCGGCGGCAGGCAGCGGCAGTAGCGGTCCGGCCGGATCGGCGGCAGGCAGCGGCAAAAGCGGCGCGGCCAGCGCGGCCGCGGACGGCGGCAAGCGCTCGGCGGCAGGCGGCGCGCAGGGACGCGTCTCGAAGCAGCCGCCTGGCGGGCGGCGCGGGGAGAACGAGTCGCCGAATCGGCGGCGCAAACCGAGACCGCTGGCCGGATCGGGTCCGTTCGCGGCGAACAAGCCGACGATCCGCTCCGTCCCGGCGCCGGCGAGTTCCGCTCTTTCCGCTGACATGGATGAGGCGGAGCTTGAGCCTCTTGCCGCGCCGGCCGATACGGCGGCGAAGCAGGCCGATCCATCGGTAAAGCAGGCCGATCCGTCGGCCGAGCAAGTCGACACAGCGGCCGCGCCGCAGACGGAGGAGAACGGGGAGTAGACGGAATCCGTCTTGTCCGTTCGGAAGGACCCGGGCAGCCTAGGAAGGTCGATTTCGTGAAAAAATCGGCCTGCAGACTCCCCCGAGTGCGATCCTCGGGCTGCAACCCGATAAAATCAGCTTGCGGACTCCCCGGGGCGCAATCCCCGGGCCGTAACCCGAAAAAATCGGCTTACGGACTCCCCGGGGCGAGATTCTCGGGCTGTAACCCGATAAAATCGGCTTGCGGACTCCCCAAGGCGCGGCTCCTCCGCGAAGCGGCTGGCCACGAAAAAAGACGTACATCAAAAAACCAGGGCGAAGCCGCTTCCCGGCCTCGTCCTGGTTTTCCGTCTGCAACCCGGCCGCGGGCTTTCCGCAGCCGGCGCCGCGCTCGGGCGTCCCGCCTTGCTTCTCTACGTCCAGCAGCGCTCCCCGGCTGACGGCCGCTCTACTCTCCGAGCAGCTCCAGCAGCTCGCCGAAGCGGCGGATGCGGACATCCGCCCCGTCGAGCTCGGACGACGCGCCGAAGTCGGCGTAATCGCAGCCGACGACCGGCAAGCCGTTGCGCTTGCCGGCATCGACGTCCGAGGAGCGGTCGCCGACCATCCAGGCGCGGGCGACGCCATGCTCTGCGAGCAGCAGGCGGACGAGCTCCGCCTTGGTCGCCGTGCCTCGGCCGCCGGCCGTGTAGAGGCCGTCGAACAGCGGCTCCAACCGCTTGTGCCGGACGATGCCCTCGACATAAGGCTGCAGGCCGTTGCTCGCCACGAACAGCCGGATTCCCCTCGCGCGCAGCTCGGCGAGCGTCTCGGGCACGCCTTCGTACAGCACGCCTTTGCCAGCCGCCAGCTCCTCCAGCTCGAACTGCAGCAGCAGCTCGTTGGCGCGCTCGCGGGCCGCCTCGGACGCGGTCGGCATCAGCTTAAGCCAGATGTCCTCCAGCAGCATGCCGAGGCAGCCGAGCAGAGCCTCCACCGGCGGCTCCGGCTCCGCATACAGTCCCTCCTCGCGCAGCGCCGCGAAGATGCGCCCATGCGCCTCCATCAGCAGCGTCTCCGTCTGCAGCAGCGTTCCGTCCATGTCGAACAGAATCACCTCCGGCCGCTCGAGCCGCACGTTTCCGGCCGCTTGTTCCGTCATCCCGGTTCTCCCCTTTCCTCGCTTTTCCCACTATAGCCCAGCCTGTCCGCCCCGGCAAGGCGCAGCCGGTCGCCCGGCAGCTCGCCCGCTTCCGCGATCCGCCGCTTCTGCAGCGGGCTTTCCCGAGGCAGATACACCTCCACGACCGTGCCGACATGCCTGCGGCTGCGGAACTCGATCGTGCCGTCATGGGCTTCCAGAATGCGCTTCGTCACCATCAGCCCGAGCCCCGTCCCCTTCTCCTTGGTGGAATAGAACGGCTCGCCGAGCCGGTCGAGGCATTCTTCCGGCATGCCTCCGCCCTCGTCGGCCACGCGCACATGCCAACCCTCCGCAGCGGCCTCCAGCTCGATGCGGATCTCGCCCTGCTCCATGACCTCGATGGCGTTCTTGACGAGGTTGACGAACACCTGCTTGATCCCGTATTCCTCTCCGAGCACGACCGCCTCCGGAAGCGGCTCCAGCCTCAGCTCGATGCTCTTGAGCAGCGCCTGCGGGCTCATCAGCGTTGCAACCGCTTCCAGAACGCCGTCCAAGCGCACTTGCTTCACGATGCTTTTCTGCGGCTTGGCCAGCATGAGCAGCTCGTTCGTGATCGAATCGATGCGGCTGATCTCCTCCTGCAGAATCTGGAACATGTAGGCTTTCTCCGGCCTTTCGTTATAGGTTTCCAGCAGCCGGACGAAGCCTTTGAGCGAGGTGAGCGGGTTGCGGATCTCATGCGCGACCGCCGCGGCGAGCTGGCCCGCCGTCTGCAGCTTCTCCGATTTGAGCAGCAGCTTCTCCGTCTCGAGCTTCTGCGTCAGATCCTTGAGGATCAAATACGCGCCGTCCCGCTGTCCATGGATCAGGATCGGCACGAACTCCACCTCCGCCAAAATCGTTTCTCCGCTCCGCAGCGGCAACGGCAGCGCCAGCGGAGACGTGTGGCAATCGGCGCCATCCCAGAGCCGGGTGAGCTCGTCTCTTCTCTCTTTGTCGAGGTTCATCAGCTCGTCAAGCCGCTTCCCGGCCAGCTCCTCCGGCTGCGCTCCGAGCAGCTTCAGACTGGCCGGATTGCATTCCCTCACTTTACCGTCGATGTCCAGCTCCAGAATGGCATCCGAATGATGAGCGATCAGCGATCGCAGCCGCCGCTCGGCTTCCCGGATCTTCAGCTCGCTCCGCTTCTGCAGCGTGATGTCTCTGCCCATGCCGAAAATGCCGATCACATGCCCGTCCACGACAATCGGAAATTTCGTCACCTGCCCGTACAGCTCATGCCCCTGGCTGTTGATGATCCGATATTCGCGATACTGAGGCTGGCCGGCAGCGGCGAGCCGGAAGTGCTCCCTCGCCTCAGGCAGCTCGTCCGGATGAAGCAGCGGCTCGAAGCTGCTGCCGATCAGCTCTCTCTCCGAGTAGCCGGTGATCGCGGCCATCGCGGGATTGACGAGCACGAAGCGCCCTTCCAGATCCATCTGGAACACCGAGTCCTGATTTTGCCGGAACAGCGACTCATAGCGCTGATCGAGACGCTGGCTGTTCTTGCGCTCCGCCGTGATCTCGCGCAAGACGACGGCCAGCCCCGGGGGCAGCGGCAGCGCCTGCACGGCGTACCAGCGGTCGGACTCGGGAGAATATTCCTCGAAGCGGGCCGAGCGGCCTGTCGCAGCCGCTTGCTCGAAGACGGGCTTCGCCCGCTCGACCCAATTCGCCGGAAACAGATCCCACAGCAGAGTGCCGATCAGCTGTTCCCGCGGCTTGCCCGCAAATTGCTCGGTCATCCGATTCGCATAGATGAACCTCCACTCCGGATCCAGCACGTACACCGCTTCCTCCACCTTGTCCCAGAGCAAAGCCAGATCCATCTCTTCCCGCAGCTCTCTGTCCATCGCGCTGTCCCCCCGTCCATGCGGCATGATCGGCAATCGTTGCCCGTTGACATGAATGTAGCGGCTCCAGTCCCGGTTAGCAAGCCAAAATCTGCCTATTGGAAGCCGGCGATCAAATAGGCGAGTGTCCTCCCAGCCCTCCCCCGCATAAGCTGTAGCATCCCATTGCAACGGAGGCGCATCCCATGTCCTTTGTTCCCGTACCGCCCGCCTATCCTCCCTATCCCTATCCTTATCCCTACCCGTATCCCTACCCTCCTTATCCGGAGGTGCTGCCGCTGCCGATACCGCTGCCGATCGGCGGCTTCGGTCCCGGCTTCGGTCCCGGCTTCGGTCCCGGCTTCGGTCCGGGCTTCGGTCCCGGCTTTCACGGCCCGGGCGGTCCCGGCTTCGGCCCGGGCGGTCCCGGCGGTCCCGGCGGCCCCGGCTTCCACGGCGGCGGCGGCTTCCATGGCGGCGGCCATCGTCCGTCCATCTTTGACCGCATCATTCCCTGATCATGCGCAAAAACGCCGGGAGCCTGCCTCCGGGCGTTTTTGCCGTCTGCCTCTATGTCCGTGCCTTCCTGTTATGTCGGGCAGCCGTCAGTAAATCTTCTTCTGCCCCATATCCGCCTTGATGATCTCGACCGATTCCCGGAAGCGCATCGCATGCACGATCTCGCGCTCGCGCAGGAACTTCAGGCTGTCCTGCAAGTCGACGTCGTCGGTGTAGTCGATAAGCCACTGATAGGTCGCCCGCGCCTTTTCCTCGGCCGCGATATCCTCGTACAGATTCGCGAGCGGATCGCCTTTGGCCGCGATGTAGGTCGCCGTCCACGGCACGCCGGCCGCGCTGTTGTAGAACAAGTCCCCGCCATGATTGACAAAGTCGGTTCCGAGGCCCGCCTCGCGCAGCTGCTCCGGCGTCGCGTCCTTGGTCAGCTTGTAGATCATCGTCGCGATCATCTCGAGATGCGCGAATTCCTCCGTCCCGATGTCGTTCAGCACTCCGATCACCTTGTCCGGAATCGTATACCGCTGGTTCAGGTAGCGCAGCGCCGCCGCGAGCTCGCCGTCCGCGCCGCCGTACTGCTCGACGAGGAACTTCGCCATCATCGGGTCGCATTTGCTGACTTTTACCGGATACTGCAGCTTCTTCTCATACAGCCACATGCCCTCATCCCCCCTCGCTGGCGTCCATCCGCGATTGTTGCTCTCGTCCATGCCCGGCCGCCTGCGGCGCGCGCTCCGCCGCCTCGGCACGGGCCCTCGCCTCCCTGCGCGGACACGGGCGGGAGCAGGCTCTGCTGCATCCCGGCTCCGCCGCCAGCGCCGCATGCCGCTCCGCCGGGCCGGGCGGCCGCTCCGCCGCTCCGCGCCGATCGTCCATGCTCATACCTGCCAAGGCCACGGCGTCTCGTTCCATTGCCAAGGATACCGGGAATAGCTGTTGCCGAAGTTGACCAGCGGTCCGAACTGCAGCTCGAACTGCTGCGCCACGGCCTGCCGCTTCTGCGCCAGCTGGTTGAACTGCTGGATCGCCTGCAAGTCCCCCGGATGCGTGTTCAAGTACAGGTTCAGCTCCACCAGCGCAAAATCCAGCACCTGAAGCTCCTTCAGTCCGGCTTGATAGGCCTCCTTGTCGAATGCCTGCTTCTGCTGCTCCTCGCTCATCGAATCCGTTCAGCTCCTTCCGCAGCCTGGCTCATAAGGACTGTACAGCGCCGGCCACAGCGTGCCGAGGCGCAGCGCCTCCTCGAGCGGATATTGAGGCAACCCCGTCGGCTGGTACAGGATGTACTGATTCGGCGGAATGACATACCGCCTGACGCCGATCGGCGGGCACGGATCGCATGCCCCCCGGAATGGAAGCCATTCCCTGTAGCCGGCTCCCGGCACGCCCGGCGGCGGCAGCTCGCCCGCTGCTCCCGCCTGCGCTCCGTAGCCCGTCGCCGCGCCGTATGCGGGCTGGCCGTAAGCGGCCGCGGCCGCCAGCTCCGCCTCGCTGCGGTAAGCCTGCTGCGGGGCGCCGAAGCCAGGGGCCCCGCCGGCATAGGCCGGGGCGCCATACGCGACGCCGCCGGGCTGGCCGGCATAACCGCCCTGGCCGCCTCCGAACATACCTCTTGCTGCCTGTAGCCTCATGTCCTGCCTCCTTGCCCGGCCGAGCCTCCTTCTGTCGACGCAGCGGCTGCAGGCCGGATGCTGTGCTGCTCCTTAAAGCGTATGAGCCGGGGCTTTTCCAACTTGCCTTTTACTTTTTGGCGATGCCATCCGATAGGACTTTGCCGGGGCTACGGCGAAGTAGAAGCGATCGCGCTCCCTGCGCCTCCTCCCAACTCCGTCCGAAAGGCAGGTCGCCATGTTCGATTCCGACATTACCGAGCGCTTCGTCGCCTACAGTCCTGCCCATCTGATCAGCCTCGGACTCATCTTCGCCGCGGTCCTGCTGCTGTTCGCCTTCCGCGGGCCGCTGGCCCGCCGCCGCCCCGCGTCCGGTCGCTACGCGCTGGCCGGACTGCTCGCCGCCTGCGAGATTCTGCTGAACGTCTGGTACGTCTCGAACGGCGTGTTCCGCCCGGAGGCCACCCTTCCGTTGGAGCTGTGCAGCATCTCGCTTTATTTGTCCGTCATCATGCTGCTGCTGCGCAGCCGGCTGCTGTTCCAGATCGTCTACTTCACCGCGATCGGCGGCGCGCTGCAGGCGCTTGCCACGCCCGTGCTCGGCTATGCGTTTCCGCATTTCCGCTTCCTCGAGTTTTTTGCCGCGCACGGTCTGCTGCTCCTGGCGGCCCTCTACATGGTCTGGGTCGAAGGCTTCCGCCCGACGCTGCGCTCGCCGTTCATCGCCTGGGGAGCGGTCAACGCGATCGCCGCCGTCGTGTTCGCGGTCAACCGGCTGACCGGAGCGAACTACATGTTCCTCGCCCGCAAGCCGCCGAGCTCGTCGCTGCTCGACTATCTCGGCCCGTACCCGTGGTACATCCTGTCGCTCGAGGCCGTCGCGCTACTGCTGTTCCTGCTGCTCTACCTGCCGTTCGCGCGAAGCGGACGGCGCGGAAGGGAGCCGGCCCGCGCCCCGTCGCCTTAGGCGGTTCCCTTGAGGAAGGCCGTACGCGCCAAAGCCCGCTTCTCCCGACAGTCGGGAAAAGCGGGCTTTTTCGCCTGCGCCGAAGGCGGCTACAGGCGGATCTTGAGCTGGAACAGGCCGGCCTTGCGCGCCGCCATGTAGATGATGACGACGAGCGGGCCGAGAAAAACGCCGATGACGCCGACCAGCTTGAAGCCGACATAAAGGCTGATCAGCGCGGAGATCGCGCCGATGCCGACGGAGTCGCCGAGAATTTTGGGCTCGATGATGCGCCGCACGACGGTGATGACGAGAAACAGCAGCACGAGGCCGAACGCGGTGCCGCTGTGGCCGGCCAGCAGCATGTAGGCCGCCCACGGCACGAGCACCGACCCGGTGCCGAGGATCGGCAGGATGTCGACGACGACGACGAGCAGCGCGATCGCCATCGCGTAGTCGATGCCCATGCTCGCCAGGCCGATCAGCGTCAGGACGTACGTCACGAGGCTGAGCAGCAGCTGCGAGCGCAGGAAGCCGAAGATCGAGTCCTTGAGGTTATCGAGCACCTGCCCGAGCTGCGGCTGGGAGTCCTCGTGGAACAGCGACAGGAACGACGCCCTCATCGTGTCGAGGCCGAAGCTGAACATGTACACCGCGACGAGGAACACGATCGTGAAGATGAACATTCCCGGCAGGCCCGAGGCGACGGCGACAACCGAGCCTGAGAGCGCGGTCGCCATGCCCGTCAGCGAGCTGGCGAGCCCGTTCAGCACCTTTTCCAGCTGCACGGCCGTCTCCGGCGGGATCGTCATGTAGACGTCCTTGGCATGCTCGAACTTTTCTCGGAAAAAGACGTTCGCATCCGCCACCATCGCCGGCGCGCGGTTCCAAAAGGCGATCAGCTCCGCCGCCAGCTTGAAGCCGATGCCGGCGGCAAGCGCCAGCAGCAGCACGGTGAACAGCGTGCTGCTCGCGGCCGCGGCCGCGAGCCGGCTCATGCCGGCCTTGCGCATCAGCAGCCGGTTGAGCGGCTCCAAAAAGATGGCGACGACAAGCGCGAGCAGGAACGGCGCGCCGACGGTGAAGCTGAGGTACAGCAGCAGCAAGCCTACGGCAATGAAAACGAGCGTTTTGATCGGCAAGGCCATTCTCCCCGGGGCTGCAGTCCCCGCAGATCTCCCTTCCGGCGAGGCTGGCCGCTGCCGGGCTCCCGAAAAGAAGCTCTCCGGACGCTCCGCGCTAGCTCTCCTCTGCCGGCTCGTCCCGATCTGCAGCGGCTTCGGGATTGCGGTAGATGCGGACGCGCAGCACGCGCAGAGGCTGGCATTCCGCTACCTCGAATGTATATTCGCGATAGCCGATTTTCTTGCCTTGCTCGGGGGTGCCGCCCAGCCGGCGGAACATCCACCCCCCGATGGAATCGACCTCCTCGTCCTCGAGATCGAGCTGCAGCAGGCGGTTGATGTCGTCGATCAGCATGCGGCCGTCGACGGTCGTCGCCTCCCCCTGGACCGTGATCGCCGGCGGCGCCTCGTCGAACTCGTCATGAATCTTGCCGACGATCTCCTCGAGGATCAGCTCGGCCGTCAGCATGCCCGCCGTGCCGCCGTACTCGTCGACGACGACGGCGAGCTGGCTGTGGCGCGCCTGCATGAGCTGCAGCACCTGGCTGACCTCCATCGACTCCGGCACGTTCAGCACCGGCCGGATCAGCTTGCGCAGATCCGGCACGCTGCCGCGGTCCGCAGTCAGCAGGTCGGCGATATGCACGAAGCCGATGATCTGGTCCTTCTCCTCGATCGCCACCGGATAGCGGGTATGCCGGGTCCGATACACCATCTCGCGGTTCTCCTCGAGCGAGCGCGTCGTGAACAGGCAGTCCATGTCCGTCCGCGGCAGCATCACCTCGCGCGCCAGCAGGTCCCCGAAGTCGAATACATTGCCGACAAGCTTCATCTCGTTGTCGTCGATGATGCCGCTCTGCGCGCTTTGGTTGACGAGCAGACGGATCTCCTCCTCGGTATGGGCCGACTCGTGCTCGCTCGCCGGCTCGATGCCGATCAGCCGCAGCAGCCGGTTCGCCGCCCCGTTCAGCAGCAGGATCGCCGGCTTGAAGATCGCATAGAAGAACAGCAGCGGCGCGGACAGCCAGAGCGACACGCCCTCGGACTTCTGGATCGCGAGCGACTTCGGCGCCAGCTCGCCGATGACGATGTGCAGGAACGTGATGACGAGAAAGCCGATGACGATGGACACGGTCGAGACGACCGTCTCGTCGGCGATGCCGATTCGGTGCAGCAGCGGCTCGGCGATCAGATGGGAGATCGCCGGCTCGCCGACCCAGCCGAGGCCGAGCGAGGCGAGCGTGATGCCGAGCTGAGTCGCGGACAGATAGGCGTCGAGGCGATGGGCGATGCGCAGCGCGTAGCCGGCTTTTTTGCTGCCCTCCGAGGCGAGCTGCGTCAGCCTGGTCGTCCGTACTTTGACGAGGGCGAACTCCGCCGCGACGAAAAAGCCGTTCAGCAGCACGAGCACGACGACGACGAGCAGGTTCAGCGCGATATCGCCCGGATGGAACTCGGTTGTCATGACGTTCGGCCTCCGTTACGGGCAGAATGCGCCGGCCAGGGCGTGTTTGCAAACACCGCCCTAGAGCACGGCCTTCTGCTTCATGAAATCGACCTCTTCGTAATACATCTGCTTCACGAGCAGGTTCGGACCGCAGCAGGCGGCAGCCGGACAATGGCAGCTGACGCTGCGGCTGAGCGGATGGTCCAGCCAGCGGGCGAACACGTCGTCGAGCCGCTCGTCCTGCACGTTGCCGAACGCCGGGATGTCGCTGAAGTCCGTCACGAACACCTCGCCCGTGAACAGGTTGACGTTGAGCCGGTTGCGGCCGTCGGGATCGTTGCGCACGGTCACGTTCGGCTCGCGCCCGAGCCGCGCCAGCAGGTCGCGGTCGGCGGGATCGGAGCTGCACGAGTAGAACGGCAGCGTGCCGAACAGCATCCACAGCTGCGGGTCGCGCGCGTCGAGCAGCTCCTCCACCGCCTGACGCATCTGCTCCTTGCTCAGTGCGGGCAGACCGCCGGCCCAGGCGCTCGGATACATCGGATGCACCTCATGGCGCTCGCAGCCCATCTCGCGGATGAGCCGGTGGATCTCCGGCATCTTGCGCCAGGTGCGGTAGTTGATCATCGACTCGGCGGAGACGAGCACGCCCGCGTCGCTCAGCCGGCGCGCGTTGTCGATCATCCGCTCGTACATCCGGACCGCGGCCGAGCGCGGCACCGAATGGCCCGAGCGCGCGAAGCCCACCTCATGGAAGTCGTCCGCCGACGTGTAGTTGAACGAGATATGCATGACGTCAAGGTAAGGAGCAATCAGCTCGTAGCGCGAATAGTCGAGCGTGACGTTGGAGTTGAGCTGGGAGCGGATGCCGCGGCTGCGAGCGTACTTCAGCAGCGGCACGATATAGTCGCGCACCGTCCGCTCGGAATAGGACGGCTCGCCGCCGGTGATGCTGATCGTCTGCAGCTGCTCGACCTCGTCGAGCCGCGAGAGCATCAGCTCGAGCGGCAGCTTGTCCGGCTCGCGCATCGTCAGCGTGTCGCCAACCGCGCAATGCTCGCAGCGCATGTTGCACAGGTTCGTGACCGTGAATTCGACGCTCGTCAGGGCATGTCGGCCGAAGCGCTCCAGGCTGCCGAGCGGGTCCCACGGGTCGTTTTGCGGGGACAGCGGCGTCAGCAGCGGTTGAAGCGTCATTTCTGGGTTCATGTTCGATCCAGCACCTTATCGTTTATTAATGAAACACTTGGCCTTTATTGTACTTCCCCTTCCCGATCGAATCAAACCGCCGGGCGCGGCCAACGCAAAAAAAGGAGCCCGAAGGCTCCCCGAAACCGCTGCCTGATGCTGCCGGAACGTTCAGGACGGCGCGCCCGCAAGCTGCGCCTCGGGCAACTCGTCGTTGACGCCGGCGATCATGCGGGTAAGCTGCAGCGACATGTCGATCTCGTACGGCGCGCGCAGCCGCACGCCCTCGTCGTCGCGCAGGACGCGCACGACCGGCCGATGCGGGCAGCTCGGCCGCACGTCGACGACGACGCCGATCTCGCCGGTCTTGAGGCGGACGGTCATGCCGACCGGATAGATGGCGACCTTGTCGCGGAACAGCTGCACCATCGACTGCTCGTACTGGGTGCCGGTGCCGGCGTACAGCGCCTCGACCGCCTGATGCGGCAGCATCGGCTCGCGGTAGATCCGGTTGGTCGTCATCGCGTCGTACGAGTCGACCATGCCGATCCATTTGGAGAACTCGTGGATCTCCTTGCCCTTGAGGCCGAACGGATAGCCGCTGCCGTCGAGCCGCTCGTGATGCTGCAGCGCGCACAGCGCGGCGGCGGCCGGCACGCCCGCCTCATGGCGGAGAAGCTCGTAGCCGTATTCCGTATGGCGCTTCATCTCTTCGAATTCTTCCCGCGTCAGCAGACCGGGCTTCTTGAGCAGCTCGACCGGCACCATCGTCTTGCCGACGTCATGCAGCAGCGCTCCCATGCCGAGCACGGTCAGCTCGTCGCGCGAGTAGCCGTGATGGATGCCGAGCATCGTCGAGTAGACGCAGACGTTGAACGAATGCTGGTACAGATAATTGTCCACCGACGCCATGTTCATGAGCATGACGACGGATTCCTTGTGCGCGGACAGGTCGTCGATGACCCGATTCATGACGTCGCGCAGCTGCGGTCCGACGAACGGATAGGCCGCTCCGCGCCTGCGCTGGGGCAAATCCATCATTTGCCGGAAGCTGGCCCGGATCTCCGTCATCGCGACCCGCATCGTATCCTCGCTGATCAGCTCGTTGATCAGGATGTCGTCTGTCGCCTCGTCCTGGATGAAAAGGAAATTGATCTGGCATTCCTGGAGCCGCTCGATGAGCCGGCTCGTCAGCTCGAAGCCTTCGCCAAGCAGGACGAGTCCCTCCCCGGAGAGAACCTTTTTGGCCAGCCTCATCCCGGGCCGGCACATGCTTAGGGGCATCAGTATCATGGACGGGTCGCTCCCTGGGTACGATTAGAATCCTATCCTGTTATCTATCGACATCGATGAGGAAAAACATTAGATTCGACAGCGTTTTTCGAGCCGATCGGCGTCGATTCGACAGATCAGCGGACGAGCCTGAACCTCGGCTCGCCGCAGCGCCGCAGCGCCTCCGGCTTGTTCAGCTCGGCGGCAAGCACCTGGCGGATGAATTCCGGCAAAAAATAGCGGACGTCCCGCCCTTCCTTGAGCGGCAAATACCCGGCGCCGAAGGTGAACATGTCCAGCGTGCCGACGTCGTACTCGCGCTCGTCCTCCAGCTCGCGGCCGCCGCAGCGGATCGACACGATCCGGCCGCCTCCGTCCGCGGCCGGACTCCAGTCGATCTCAAGCCCGTCCACGGCCAGCGTGCCGAGCACCGTGCCGCGGAAGCCGAAGCCGCGCAGCTCCTTGCCGTAGAACTCCGGCTGCAGCGACTGCTCCACGGCCTCGCGGATGCGCCGGCCGATGAGCCGCATGCGGCAAGGATTGACCGGCGACGGGCATAGCGCATGCAGCAGCCCTTCGCTGATCTCTCCGGCCGGCAGCCCGCCGAGCAGCTGCCCGGCGTTGACGAGGCCGATGTCCGCCCCGGTCCACTCGCGCACGCCGGCCGCCAGCAGGTTCGCGAGCGGCGATTCGCGGGCCGGGTCGAGCTCGAGCGGCCGCTCGAGCGTGGCGGCCGGACGCGACAGCTCGCGCCGGGCCGTCTCGCCGTGCTCGCTCAGCAGCTCGGCCGCCTCCTCGTCGATCGGCAGCGAGGCGATCGGCAGCAGGCGGCCGGCCGCCTCGAGCCGCCCGCTCGACGGATCGAGGCCGAGCTCGACGAGGCCGAGCCGCTCGCCGAACTTGCCGGCTCCGCACAGCAGCGCGCCGCGGACGCGCTCCGGCTCCTCCAGCAGATGATGCGTATGGCCGCCGAGAATGACGTCGATGCCGTCGATCTCCTCGGCCAGCCGGCGGTCCACCGGCAAGCCGAGATGCGACAGCACGACGACCGCGTCCGCCGCCCCGCGCAGGCGGCCGACCTGCTCGCGGACCGCTTCGAGCGGATCGGTGACGGTCCAGCCGAGCAGGCTGTAAAAGGCCGGGTAGGCCGCAGTCGCGCCGATCAGCGCGACGCGCAGCCCGTTTTTGACGAGCACCGTCCCGGCCAGCAGCCACTCCGGCCGCTCGCCTGTGCGCGCATCGAGCAGATTGCAGCAGAGGATCGGGAAGCGGGCGCCCGCGTAGATGCGCTCCAGCTCGTCCCGGGTGAACGTCAGCCCTTCGTTGTTGCCCGGCACGGCCGCCTCGCAGCCCGCCGCGTTCAGCAGCGCGATGTTGACGGAGCCTCCGGTGCCTTCGGTCTCCTGCCGCATCCGGTCGAGATGGTCGCCGATGTCGACGTACAGCACGCCCTGCTCGCCCTCATCCCGGCGCGCGTCCTTGACGGCGGCGGCGATCCGCCCCGCCTCCTCCAGGCGGCTGTGCACGTCGTTGCTGTGCAGCAGGAGCAGCCGGCTTCGTTTGTTGTCCGTTGATCGTTCCATGCGCGCGCTCCTTCCATGCCTGCCCTTTTTCGCCTGCGTGCCGGCCGGCGGGCGGCTTCAGCGGCGTTTCCTAAGGTCCTCCGGCGAAAAATCCGACTTGAAGCCGTACGCAGCGTCGCCGCCGAGCTCGGGCTCCTCCAGCAGCGTCAGCGAGACGACCCGCTTGACGTTCAGGCATTTGCTGCTGCCGTCCGGCACATAGAGGCGCAGCGGCCCTTCGCGCTCCAGCGGCACGCCTTCGCGGGCGAACAGAAACGCCGCCTGAGCGGCCTCGCGCCAAGAAATGACCGCTTCGAAGCGGTCATCCGCGACGACCTTCACATGGGTCGGCGCCGCGACGACGTCCTCTCTGCCGGCTGCGGCCGCCTGCTCCAGCCAGCCCCGATGCCAGTCGATCAATCCGAAAGCCTCGCCGCTGCCGTCCGGCACCCGCTCCAACAGCGGGAAGACGGCGCCGGCCTGCTCCGCCATCATGCGCGCCGAGAGCGACTCGGGCGCAGCGGCCCGGACGCCCCGACGCTGCTGCCGGATTTCAATTTCCTTTGCCATGCTCCATCTCTCCTATCCGCTGCACTCTTGCTCAGCCGCCGATCTGCGACATCCGCCGCGACGTCGGGCTATGGCTGAGCGCCTCGCCGTGCAGCCTCGCCGCCATCTCATGGTTCTCCGGCTTGATGTCCGCGGCGCGCCGGAACAGCGCCTCGAGCGCCGCGCGGCTGCCGAGCGCGGGCTTGACGTTCAGTTCGTCCACCCAGTAGAGGCAAGGCTGCAGGCTGCCGTCCGCCGTCAGCCGGAGCCGGTTGCAGCGCGCGCAGAAACGGTCGCTGACCGGATGGATCAGGCCGAACGAGCCGGCCGCCCCCTCGAACGCCCAGTTTTCCGAAGGGCCGTTGCCCCGGAGCTCCTCGAGCGGAGCCATCGGCAGGCCGAGCTCGCGCGCCGCGTCCATGACCGCCGTCAGCGGCAGGTACGTCCTGCGCCACTGCTCGTCGGCATGGCCGATCGGCATGTATTCGATGAAGCGCACATGGAGCGGCTGCTCGACGGACAGGCGCAGGAAGCTCTTGATCTCGTCCTCGTTGATGCCCTTCAGCAGCACGCAGTTCAGCTTGATCGGGCCGAGCCCGGCTTCGCCGGCCGCGCGAATGCCCGCGAGCACCTGCTCCAGCCCGCCGCGCCGCGCGATGAAGCGGAAGCGGGCCGCATCCAGCGTGTCGAGGCTGATGTTCACGCGGTCGAGGCCGGCCGCCTTCAGCGCGGCCGCCTGCTTCGCGAGCAGCATGCCGTTCGTCGTCATCGAGATCTCCTCGATGCCGGGGATCGCCTTGAGCCGGCGGATCAGACCGTCCAGGCCCGGCCGCACGAGCGGCTCGCCGCCGGTGATGCGCAACCTCCGGAAGCCGAGGCCGGCCGCGGCCTCGACGACCTGGACGATTTCGTCGTAGCTCAGCAGCTCGGACGAGTCGGCGAACTCCATTCCTTCCTCGGGCATGCAGTAGAGGCAGCGCAGGTTGCAGCGGTCCGTCACCGAGATGCGCAAATAGTCGTGTATTCTTCCGAATCGGTCCCTCAGCATCGCGTTTCCCCCTCGGCCGGGCTTCCTGCCGGAAGCCTGCAGTTTCGTGTCTATCAGTTTATCATTTTTGGCGGACTTATGATATGCTGGAAGCAAAACCCCGCGGGGACAGGTGAGGTTATCTACCATGAGCTACAGCTGGAGCATCGCTTTGTTCGCCGGCTTGCCGGAGCGTCTCGGGACGCGGCAGGCCGAGCTCTCATCCGACCGGTCCGAGATGACCGTCGGCGAGCTGAAGGCCGCGCTGAGCGAGGCCTATCCCGCCCACGCCGGCTTGATCGCCGTCTGCTTCGCGGCCCGCAACGAAGCTTATGCCGCCGACGGCGAGCTCGTCCGCTGCGGCGACGAGCTCGCGCTGCTGCCGCCGGTATCCGGCGGCGACGGCAGCGGCGCTCCTATCGCGGCGGCAGCCGCCTGCCGCATCTGCGCCGAGCCGCTCGACGCGGCCGCGGTCGCTTCGCTGGTCGAGCATCCCGACCACGGGGCGGCGATCGTCTTCATCGGCACGACCCGCGAGTGGACCGCCGGACAGCGGACGGTCAAGCTCGAGTACGAAGCCTATGAGCCGATGGCGCTGCGCACGCTGGAGCAGATCCGCCGCGAGCTGGACGAGCGCTGGCCGGGCACGCGCTGCGCGATCCATCATCGCATCGGCGTCGTCGGCATCGGCGAGGCGAGCGTCGTCATCGCCGTCTCCGGGCCGCATCGGGCGGCCGCCTACGAGGCGAGCCGCTACGCGATCGAGCGCCTCAAGCAGATCGTTCCGATCTGGAAGAAGGAAGTGTGGGAGGACGGCTCGGAGTGGAAAGGACATCAGACGGGGCCTTGGAATCCGCTCTCGGACCTGGCTCCGCCGGTCCCGCCCGCAGCCTCGGACAAGCTTCCTGCGGAAGAAGCCGCGGCTGCGGTCGGAGCCGAGCGGGAGCTATCCGAATGAGCGAAGGCAGCCGGCCGGCGCTCCCGGACCGCTACATCCGCCAGACGCGTTTCGCGCCGATCGGCCCGGACGGCCAGCAGCGGCTCGGAGGCTCCGTCGTCGCCGTCGTCGGCGTCGGCGCGCTCGGCTGCGTCATCGCCTCGCATCTGGCGCGCGGCGGCGTCGGCGAGCTGCGGCTGATCGACCGCGACATCGTGGAGCTCAGCAACCTGCAGCGGCAGCTGCTGTACGACGAGGACGATGCCGCCTCCAGCCTACCCAAGGCGGAGGCCGCCGCGGCGAAGCTGCGCCGCGCCAACAGCAGCGTCTCCATCCGCGCCTATGCGGCGGACCTGCATGCCGGCAACGCCGACGAGCTGCTCGGGGGTACGGACCTGATCCTCGACGGCACGGACAATTTCCACACTCGCTATCTCCTCAACGACTATGCCGTGCGCGCCGGCATTCCCTGGATTTACGGCGGCGCGGTCGGAGCCGGGGGCATGACGATGAGCGTGCTGCCGGACGCCGGTCCGTGCTACCGCTGCCTCTTCCCCGAGCCGCCCGCCTCGGGGCTGGCGGATACTTGCGAGACGGCAGGCGTCGTCTCGCCGCTCGTCGACGTGATCGGCTCGCTGCAGGCGATGGAGGCGATCAAGTGGCTTTCCGGCCGGCGCGAGGAGATGCGGGGAGACCTGCTGCAGCTGGATCTTTGGCGCAACTCGTGGATGCCGCTCGGCGTAGCCGGAGCCAGGCGCTCCGACTGCGAATGCTGCGGACGCCGCGAATTTCCGTTTCTCGAGCCGGAGGAGGACATGGCGGCGGCGCTGTGCGGGCGCGCCACCGTGCAGATCCGGCCGGCCCGCAGCCGGCCGCTCGATCTGCCCGCGCTGGCCGAACGGCTCGCGATGGCGGGAGAAGTCCGGTTGACTCCCTACTCGCTCCGGTACGAGCGGGACGAGCGGATTTCGGTCGTCTTTTTCCCCGATTCGAGAGCGCTCATCCAAGGCTTGGAAGATCCTATTAAAGCGAAAGCCGTTTATGCCGATATACTAGGATGATAATAGGTCGGACGAACGATATTGCCCCGCTTTCAGATCCGACAATAGTAGCAGACGGCACGATGCCGTCCAAGACTAACCTTGCCGAGGTGCACCATGAGGGTTCATATTTCCGATCTAAAGGAAGGCGATCTGCTGTCTAGCGACGCCTTCAACCATTTTGGCTTGAATGTCATGGCCAAAGGAACCCGGCTGACCTCCTACGAGATCGCCAAGCTGACGCAGCACAGCATCGACTATGTGGAGGTCGAGATGGAGGCGCCTGTCGCCGCCGGATACCGGACGATCGAGTCCGGCCTGCCGCCGCGCTGGCTGCCGTCCATAAAGCCCCTTTACGAGAACGCCATCTCCGGCTGCGAAAATCTTTTCCGCAAGGCGCTGGAAGAAGGCAAAGTGAGCGAAGAGGACGTGGACCGGTCGTTCGGTCCGCTCATGTCCAGCTTCCAGATGGAGAAAGACGTCGTCTCGATGCTGCTGCTGCTCAATACGGACGACGACTATACGTACCAGCATTCCGTCCAGGTGGGCATGCTGTCCTACTACCTGGCTTCCTGGCTCGGCTTCCCGGAGGAAGAGGCGGCGCGCATCGGCAAGGCCGGCTTCCTGCACGACATCGGCAAATGCCGAATCTCCAAGGACATCCTCAACAAGCCGGAGAAGCTGACGAGCGAGGAGTACCGCGAGATCAAGCGCCACACGCTGTACGGCGAAGAGATCATCCTCAGCACCTACGACGATCCGTTCCTCTCCTCCGCCGCTCTCCAGCATCATGAGCGCATGGACGGCACCGGCTACCCTCACGGCATCGACGGCATCGAGATTTCCCCGATCGCCAAGATCGTCGCCGTCGCGGACGTGTACAGCGCCATGATCTCCACCCGCTCCTACCAGCAGAAGCGCGACCTGCTCTACGTGCTGCGCGAGCTGTACCGCATGAGCTTCCACGAGCTGGATCCGCACACGACCCACACGTTCATCCGCCATATGATTCCGAACTTCATCGGCAAAAGCGTCGAGCTCGACAACGGACAGTTCGGAACCTTCATCATGACGCATCCGAGCGAGTTTTTCCGCCCGCTCATCCAGGTCGGCGAGGATTTCCTCGACCTGTCCGAGCAGCGGGAGCTGGAGATTACGCAGATTTATATGTAAATTGAAAAGACCCCCTAGCCGCCATGAGGCGGCTAGGGGGTCTTTTGCATGCAGGGCGTCGGCCCGGACGTTCGCTGTCCCTCGTCAGTCTCCTCCGCCGCAGCTGCTGGACGAGCAGCTGCTCGAGCTGCAGCTGCTCGAGGAACAGCTGCTGGAGGAACCGCCGTCGGAAGAGCCATCTCCGCCGCTGTCCGAGCTGCCGCTTCCCCGTTCGTCGAACGAGTCGCCGCCCGCGCAGCCCGATGCCGAGCAGCCGCTTTGGGAACGCTCGCGCTCCGCCTCCGGCAGATGCCGCTCCATCTGCTCGTCGAACGAGCCGCCCATCGAGCTCATGAGCAGCGCTCCTCCCAGCATCGCTCCGTAGCCGGGATCGGCATAGCTGCTCCCGGACAATCGGCCAGGCGAGTCGCTGCGATCGGCGCTTCGAGCCTCGCGCGCGTCGGCGGCCTGACGGCGGAGCTTATCCAGCATATAGGAGACGAGCCGCTCGTCCGCTTCGGGACGGAACAGCTCCGAGCGCAGCTCTCGCGGCTCCGCGTCCTGCAGCCGCTCCAGCCTCTTTGCATTGAGCGGATGGCGGAAAAAGGCTCCCCAGGCGACAGGAGCGAAAGCGTGGAAACGGAACAGCGCCGCATAGGCCAGATCGAACCAGGCGCGACCTCCGGGATCCGGGACGCTTTCGGCCGCCGGCGCGTGATGCAGCGGTCCGCCGATCAGTTCTTTGCCGAAGCGCTCGTATTCGCGGGTGTACATCAGCATCTCATGCCAGACCCCGTCCACCTCGTCGCCGAACATCGGCACGGTACGCAGCAGCGAGCAGAGCACGAAATAGCGCTTCAGCTCCAGCAGCAGCAGCTCGAACCGCTCTGGCGAGCAGTCGGGATGCTCCGTCAAATAGCGCTGCCGGAGCTGCTCGACATAGGAGGCGGGCAAAGCTTTGTCCAGCTTGGCCGCCGTCGCTTGCAGCGGCGCGTCCGGCAAGGCGCCGAGATCCAGCCAGCCGGCGGTTTCGCGGGCGGCCTCGGCGACCGCGTTCCGACGCGGATTTTTGGAGGAGGACAAGGGACGCTCCGCCGATCGGCGAGTTTTCGTTCGAGCCGATACGAGGGACAGGACGAGCAGAGCGAAGAGAGCGAGCAGAAAAAGGGAGCTTGGAGTCATCGGCTTCTCCTTTCGAAGAGGAAGAAAAGATAGCCTTATCTTACCATAGCGCGGATCCGCTCGGGGGAATGGCCGCGCAGCGGCGCAGCTCGTCCGCCATGGCGCGGAAGCGGTCCGGATTCTCGCCCTTGGCGCGGGTCTTGAACCAAGCCGGGGACAGCCAGCCGACGATGATTTCCTGCGCGTTGCTTTTAAGCAGCCTTTCTCCGTCCACGCAGCGGCGCAGGCGCTCGGCCAAGCGGGCGTAGTGCGCGGCGCCTTCGCTGTCTCCCGCCTGGATACGCTCGTGCCACGCCGGCTGGATGTAGGAGCGGACAAGATGGGAACAGGTGGCGGCAGAAAGGGCAGCCGGCGAAGAGGCCGCAGTCGCGCCGTCTTGCTGCGTCTTGGCCGAATCGGCGGCCGCTCCTGCTTGATTCCGCCCGCTGGAGCCGGCGGAGGAAGGCTCGGCTGGGCGGGCGGAGGATTCCTCCGCTTGGACGGCCGCCGCCAGCTTGCGCTCGACGTCGCGGATCAGATCGGCGAGCGTGCGGCCGGCCGTCGCCAGCGCCTGCTCGCAGTCGCGCTTGCGCGTCGGATCGAGCTGGCCGTGGCTCACGATATGCGTCGAAGGAACCTTGCTCCACTTGGCGCAGCAATAGGCCAGATAAGCGACATAGCGGTCGTAGGCCGCCTCGAAGCGGATCGCGCCGCCGTAGCACAGCTCGATGCCGAGCGCGGCGTCGTTGGCGTCTGCGCCGAAGCGGCGGTTGTCCTCCGGCGCCTGCCTTTGCACATGGTACGCCTTTTCCGCCGGGTCGTCTCCCGTGCCCGTCGGGATGATCTCCAAAATCCGCGTGTCGTCGATGAACACATGGGCCGAAGCGGTCCGCTCCGTCTGGCGGTCGAAATAGCGGTAATGGGCTTCGGCCGTCGCGCCCGGGTTGCCCGTATCATGAGCGACAAAAAAAGCCGGGCTTCCGGCGGTCAGCCGAAGGCCCGGCCTCGTCTGCGGACGGATGCGGATGTAGCGGCGCTCGATCGGATAGCCGAGGTCAATCATGGGCGTCTTCCTTGCGCAGCGCCTGCGCGGTCTGCTTCACAAGCTGGTTGCCGTAGACGGCGACGGCGCCGCAAAAGATGCCCTGCATGACGCCGTCGGCGGTCCAGCCGGCCGTGAAGCCGGCGAAGACGATGCCGGCCGCGGTGACAAAGTAGATGATCATCCAGTCCCGGATGCCGGCCGTCCGCTTGAGGCCGTAGCCGATGATCCAGCAGACGGCGACGACGCCGGCCAGCTCAGGATGGATCATCGATTGGATGAGCGTCCAGTCCATCTGGCTTCCTCCTTTGGCTTCGCTTTATTCGAGTATTTTGAAAACGAGGCCCAGCAGCGAGGCCGCCAGGCCGATAAGCGTGAACGAGGTCGTGATCAGCCAGCGCTGGCCCTGCTTGATGCCGTCGATGCTGGCTCGGATCTCGTCGATCCGGTGATGCGCGGCGCGCGCCCTCTGGGCGGCCTCGCGCGCCGTCTCGTCGCTTTTTTCCAGGCGTTCGATGAGCCGCGCGACTCCGGAGGCCAACTCGCCGAGAGCCCGAGTGTTGACTTCCTGCAGCGTCTCGAGCTTCACCACTTGGGATACGATCGCCTGGAGCTGGTTCTCGGGTCTGCTCATGCCGGGTTTCTCCTTTCGAACGGGGGAGGGAGACGGGTTTATCAGACTCCAGACGGAACTAAACCTTCATCTACGCCTTCCTTAATCTTGATTTTCGTAGTCAAATAGTTGAGCAAAATGGAATAGTAGCTCAGCACATTGCTCTCTCCGATTTTTCTGATTCCGTCCGTATATCCGTTGAACGTATTTGGAGAAAGAGCCAGACTATCAGACAAGTCCAGCTCATCATTTAAAGGCAAAACCAACATTGCATTGCTAAGAAGAATTGATCCGGATTCAATGACTTGATAGCTGACTCGAAACTGGCTTACATTCCCCTCCATGTCGAAGTTCTGCGTTACCGCCAGCAATTTGATTTTTTTCCCCATTGACTTAGCCTCCTTAAGAGTTAAAAGCCTTGTGCATGGTTGAACCGCAGAGAATGGTATCCCCTTCTCCATGCCGCTATTCGGTACATGAACCGCGAGTTGGGTTTCCCCTTAACCATAAAGCGGTCCGTATAGCGTTCGGGAACATAGAACGCTCCTTCATCAATGCTTTGAATGAAAACGTGGTAGTCTTCCCCTTTGATTTCAACCGTTTCGAGAAAGATAGGATCCATTGAAACGATTACCTGGCCTTCTTGATCCGTCATGGCCTCACCATAATCCTCAAACCGATTTTCGGGCGACTCTATAGCAAACAGATATTGATCCCCATAAGTGGAAGTTGATACGACAGCCGATTTGGTTCCTGCCACACTGAACGATTTTTGAACTCGGACTCCTAAGGCATCCCAGTAGGCGCTTTGCTGACCTGCTGCGTACATCGAGATGCTGTTGTCGCCATTCCATAAGAGCCCTGTATCATGATCACCAATCGATAGATCGAGAGCGGCTTGGCTGTTCATATTGTTTCTTCCTGAACCTCCATTGAACCCTACCGCAAGTGTGCCCGACACCCGCGCGTTCCCCAACCCAGTTACTTTAAAGAAAGGCTGCCAAACCCCTCCTCCTACAGTTCCAACATCTAGAATAGCATTCGAGTCGGCCATATATCTGCTTGCAACGATCAATCCAACAGCGGCCGGATGATCCTGCCAGTTCACGATCGAAGAAGCTGGAGTAATGCCTGCCGGAGGGAACGCCGGAGCTGAGTTGGCTGCTTTTGCATGACCGTGGCGTTCAATTTGAACGGCAGTTCCGTTCGAAGCGGACGGACCGCTAAGTGTTAGAATCGGAGTCCAGTTGATGGTGTCGTAAAAAGTTCCCAAACGGATCGTATTGTTGCCTACCATTCGGATACCATCTGTTGAGCCTATGTTTTCATATACCGCGTAATGTTTTCCATCTGTCGCATTTTGTCCGCGAAAATAGATTGGCGAGTCGGCAAGGTTGAAATTGGAGTTGCTTCCTCCTCCCAAGTTCAGCTTTTTAGGGATTGTCACATTGCCGGTGGACCGAGCTATATCCAGTCCTTTTGTGATGAATGCGCCGTTATTGTCATAGGTCCAAAAAGAAAGATTCCCTCCCCCATTGCCAGCGGAACTAGCTCCATCAAGACCAATTCCCCCATAAATATTTCCATTATTCTTCATTGCCAAATGAACATTCCCACCACTTGAGGTTCCTTGCGTCGTGTTGATGGAATCAAAGCTTGGAATCGCTGATTTCCGAACATCCTGATCAAAATGATATCCGTCCACCATATCCGCATTGAGCCCCGATCCTGCGCCGCCGTTCCATTTAGCCCGGTCGGCAGTCGAAACGTGAGATGCTTGACTGGATGCATGCGCGGTCAAGCTGCTTTGCACCGCATCCACCTCCGCCTTCCGCGCCGCGTCGTCCGCGGCCGCCGGGGCGGCCACCTTGACGCGGCCGGCGGAGTCGCGCTGCATGAGCTTGCCTGGCGATGCCGCGCTCGTCGCCCCATGCGCGCCCTCCACGACCGCCGCATGGGCGGACGCGGCGTTCACCTCGCCGCCGAGCGCGTTCAGATCCGCCTCGGTGACGACATCGTTGAATTTCCAATCCGTCTTGGCCATCGTCATCCCTCCTCTACCGTGATCGACTGCAGCATCAGCGTATCGCTCGCAATCGGGATCTGCACTTCGCTTACGCTCAGCGTCTTGCCGGACGCATCCTGCAGCTCGATCCGATGCACCGTGCCTACCGCCTCCGCCGGAATGTAATACCTCAGCTCGACAACTCCCTGCGACGCCCGCTTCAGCGTGAACTCCGTCAGCAGCACCGCGCCGCCGTTGAGCGAGACGCGGGCGATCCGACCGTCCACATATGCGGCCACGTCCTGGATCAGCGAAGCCTCCATCATCGTACGATCACCTCTTCCTTCTCTGTCGTGAATCCGGTCGCGCCGAGCTTCCAGCTGCCGAGCCTCGTCTCGCGGGCCAGCCGCCGATAGCGGATGCCCTCCCTCAGGCGCAGCGTATCCGCAACCGCCGTCTGCTGCACATAGACCAGACTCGCCGGCTTCAGCGCCGTCACCGTCTGCTCCACCTCGCGGAACAGCGGCGCGTTCTGGATCGCGGCCGAGATCGTCAGCACCTGCGCCTCCAGGTCTACCTGCGCCAGCGCGCGGCCCTTCCCGACCAGATCGTCCAGCCTCTCTTGCAGATACCGCAGGGTAAAAGGAGGCTTCGTGGAATACCGGTTGACGACGCGCACGCGCCGAAATGCCAGCGATTCCTGCGCCTCGTCCGCCCGAATGCCGAGCAGCCGCTCGTGGCGGCGGATCGCCTCCACGGACGCGGTCAGCACGAAGCGGTCATCCAGCAGGCGCTCCAGCGCCTGCTCCGCCGAGGCTATCTCTTCATCCTCCGAACGGAACAGCTCCGTCATCTCGCGGCTGTCCGAATAAAACGCCGGCAGCCTTCCGATCAGCGGCTCAGCCATTCAGCGTCACCGTCCCGAGCGTCGGCACCTCGTCGGCTTCCAGCTCCAGATTGGCCGGCGCGCCGTTCAGCGTCGTGCCGCCGATGTCCTCGACGCCTGGCAGCGCCAGCACTCTCGTCTCCAGCTGGGAGATGCGCACGATCAGCCGGCTCTCTCCCGCCCAGGCTCGCCGCAGCTCCAGCAGATACGCTTCCGCCGCCGCCTCGATGTCCCGCTCCAGCTGGACCGCGCTCACGCCGGCGCGCAGCGTGAGCTGCGTGGCGATGTCCACGGGAACCGCGTCCGCTGCCACGATCGTCACCCGATGGCCGATCGGGGCGAGACCGATGCCTTGTCCCGCCGACTCCGGGTCGATCGCCGCCTGCACCTCCTGCACCAGCGCGGCCGCCGCCGGAGCGAAGTCGCTGGCGATTACCGTCGCCTTCACGGTGCCGCCGCCGTTCCAAGCGGGATGGATCTTGACCCCGCCGACTCCGGGCAGGCCGCCGATCTTCGCCCGGTAATCCGCGATATTGCCGCCGAAAGGCTGCTCGCTGACCGCTTGCCAGAAGCGGGCCCGCAGCTCGGCGTCTCCCTCCTCGTCCTCGCCCGGCACGAGCACGTCCGCCAGCTCGGCGCGAGCCAGGCCGTCGATGTAGTCCAGCGGCAGCAGCGCTCCCGCCACCTCGTTGCCGGCTCGGCCGGGCAGCTCGGCCACGAGGCGATACGTCCCCGGCGCGAGCCGCTCCGCCACCTCGTAGGCGGTCCCTTCGGCCGCCAAGCGCGAGCGCAGCGGCACCTCCGCCGGGCCTCCGGCCGCGCCGAAGAACCGGCCGAGGCGCATCGCCCGGCTCGAGGCCTTGCGCCGCACGCCGTGCTCGGCGGCGCGGCGCGTCAAATACTCCCCGTCCGCCGTATCGGCGAACGAAAGCGCCAGCTGCACGTCCAGCTCGGCGTAAAGCGCCGCCAGCTCGGCCGCTGCGGGCGCGAGCGCGTCGAAGATGACGCTGCCTTCCCTTTTGTCCAGCTCATCCGGAATCCGGGCCAGCATGCGGCCCATGATCTCGCGGTACGTCTGATGCTCATACACCGGCCATCGCCTCCTCCTTGAACGAGCCGAAGACGGTGCGCACCGTGAACGTCAAGGACACGCCGTCTCCTTCCCGCCTCATCTGCATGTCCTCGACCGCCAGCACGCGGCTGTCCGCCAGCAGCGCTTCCTCGACCGCGGCGGCGATGTCGTAGCTCGACCGCTCGAGCCCGACCTCTCCCGTGTACACCTCATGCTCCCAGCGCACAGTCGACAGCTGCTTGAAGACGAACTGGCGCATCGCGGCCAGCCCGTCGATCCTTCCCCCCGTGCGTCCGTCCAAATGGATCGGGTACGTCAGGCTCGGCCGCTCGACCGCCTCCGCCGCCGTCCAGTCCAATCCCGTCTGCTCCGGCACGCTCATGCCTCCACCCTCCCCAACGCCACGTAAGGGCTGCCGCCCTCCGAGCGCAGCAGGACGAGCCGGTCGCCGAGCTCAAGGCCGCGCCGCAGCACGACGCGCTCCCCGCCCAGCTCCACCGCCAGCTCCCGCAGATGCTCGGGCACGACGAGCAGCTCCGCCGGCAGCGTGAAGCGCTGCTCGACGGCCACCTCCAGCGGCTCGAGCCCCGTCACCTTGCCGAATACCGCCTTCGTCAGCTGCTGCGCCTCCAGCGAGCGCGCCATGATCTGCTTGATCGAATCGTTGATGCTCATGCTTCATCCTTCCTTTACCATGCCGTCGATGACGTACAGCTCGAGCTGCATCGTGTGCGAGCGGCCGGAATAGGCGTGCGTGCATTCCTCGACGAGAAAGTTGCGGTTCAGCTGCAAGCGAGGAATCGTCACCTGCACGACCGAGCCGGCGCGGATCGTCGGATGGCCGAGCGCCTCCAGGCTGAATTTCCGCTGCTCGCGGTTTTTCAGCTGGAGCAGCTGCTTCAGCATCTCCTTGATCCGCTCCTCGTTGAGGCCCTCGTCCACCTTCTGGTAATATTGCAGCTGTCCCCAGCGGGCGATCGCGGCGCCGTCCTGCTCGATATAGACGTCCCGACCGCCCGTCTGCTTGTTGTCGCGCACGAGCTTGATGCGGTTGTACGTCTCGCTGTCGATGCTGCGGCTGGACGAATAGCCCGTCAGCAGGCTGTTCTCGCCGATGACGACGCTCGCCTTCATGTCGGCCACGTCGCGCAGCGTCAGCAGGCCCGCATCGTCATAAAAGACGAAGAGCTTCCCCTTCGCCAGCAGCGTCTCGTCCAGCGCCTTGAAGATCATGTCCAGCCGCTTCTGCCCGTCCTGGCTGAACTTCGGAATCGGATGGCCCGTATCCGCGATAGGGCCGAGCCGGGCCTGGATGGCCAGCGCCTGGTCGCGGATGACCTGAGTCGCCGTCACGTTCGTGCGGACGTAGGTATCCGTCTCCAGCAAATAGCGGAGCTGATCCTGGGCTTTCACCCGCACGACCCGATCCTCGTCCTCCTCCAGGGTAAACACATAGCCGTAGAACAGCCGCACGCCGCCGTCGCTCACCCGTACGACGTTGCCGGGAGCGATCGGCAGCTGGCTTTGCGCCGCCAGGCTCGGCCCCCGCATCATCGAAAACTCCAGCGTGCCCGCCTTGCCGATGCGGGACGTCTTCCAGCTCAGCTCGGTGGCCATGCCGGTGACGTCCCACAGCCGTCCGTCGCGGAGGTCGAGCTCAATCTTCAGCATGCCCTCACTCCTTCGGCGGCGGCACCTGAAGCACGCGGCCGATCTGCAGCCGCTTCAGCTCCGAGTTGCCGATGCCGTTCAGCTTTTGGATTTCCGGCCAGCGGCTGCTGTCGCCGTCGTACAGCTTCATGCTGATGCCGCTGAGCGTGTCGCCCTTGACGATCGTGTAGGCTTTCGGCGGCACCTTCAGGTCCGGCCGCTTGTCCGGCTCCTTCGCCACGGCGGTCGAGCCGTCCGCCGTCTTCACCGCCTGCAGCTTCACCGGCGCGTAGAACACGTATTCCTTCAGCTTAAGCGTGTAGAACACGTCGCCCGGCGAGCCGGCCTCCTCCCAGCGATCGAAGCCGGTGATCGTCATCGGAATCTGCAGCGTGTACGGATTCTCGAACCGGTCGGCATGGCGGGCATAGATGAACCGCAGCGGATAGCCGGAGCGCATCCAGCGGCCGATGTCGTCGGCGAACTGCTCCGGACGCTTCAGGATGGACCGGGTCGCGACGTAAGGGCCGGGCTGGCTGGGAAAAAAGCTCTCGAACTCGACCTCGGCCAGTCCCGGCTTCTCGATCGTCGCGATCGGTCCCGCTCCGAGCAGATTGTAGTCCTTGCCGGAGCCGCTTCGGCGGATCGACAGCTTGGACGGCAGCACCGGCAGCTCCCAGCCCTCCGTGCCGTGATTAAAGTCGAGCCGGATGCCGGCGAACGCTTTGGCCGGCTGAGGGCTGACCCGAATCGGTATAGCCATCGGCGACCTCCTTTCCGCGCAATGCTGCGCTTCGTAATGTTGCTAAATGCGGGCGTACACCCCGTGGGCGGACGACTCGATCTCCTGCTCCATGCTCGCGGCGATCTTGCGCACGACGTCGTCGACGTCGACCTGCTTGTGGATCGGTCCCGTCGTCACCTGCACCGTCGGCGTCAGCGTGACGAAGTTCTGGATCGCCTTCATCTCGGCCAGATCGCGCATCACCTTCAGCTCCTCGCTGCCGATGTCGACCTCGCTGCCGATGCTGCCGACCTCGTTGACCTTGCCGATGTTGGGAATGTTCCCGCCCGGCGCGGCTCCTGCTCCGGCGCCGCCCATCATGCTGTTCTGCTTGTCGGCCATGCCGCCTCCGCCGCCCAGCTTGTTTTCCCCTTTGAACATTTCCTTCAGAGGATCTTTCTCCCCGTTGAAGAGCGAGCCTGCTTTGTCCAGCGCTCCTTTGCCCAAGTCGTAGCCCTTCTTGCCTGCCGCTGATGGATCCAGCGCGTCCAACCGTCCGATGCGGACGGGGTCCTTCTCCGAAGTCGGCGGCTCGATTTTATCCAGCATGCCCTTCAGCTTGCTGCTCAGGGCATGGGGATCCTTTACGTCCAGCTCTGCGATGCCTTTGTATTCTTTGCCGAACAGCTTCGCCATGCCGGCTCCCAGCCCGTTCACCAAGCCGATGACTCCGTTGATTCCCTCCAGAATGATCTTCATGAAGCCGCCTGCGAAGGACTCCGTCATGAGCAGCATTTCATACAAGGCGTTGCCGAACATCATCGCCAGATCGTAGAACAGCTTCTGAACCGCATATACCGGATCGATGAACAGATTGATCAGGAACTCCGCGAAAGTCGCGAACAAGTTCCAGGCAGACGCGATCATGTTATAGATCGTGGCCCCTAGGAAGAAGAACAGCCCGACGATGAAGCCGATGATCTCGCCTGCGCTCGTCCCCGTCTGGAGCAGCGCGTAAACGAGCAGCCCGATGATCGCAATGATGAGCAGCAGCGGCCAGTTCGCCATGAAGAAGGCAGCGGCCATCGCCATGATCGGCGCCACCATGCTCCATAGCCAGACGGCCATGAGCGGCAGCAGCACCGCCGTCAGCACGGTCAGCACGTCGCCGATCGCATCCCCGTTCGAGACGAACAGGTTAATCAGGAACAGCGCGGCATCTGCCGCTGCGGAGAGCAGCTCCGCCATGATGTACAGTCCGGCGGAAAGCGCGTCGAAGAAAGGATCGAGCTTGCCGGAGTCGAATACAGCCATGATCTTGTCCAGAACCGGAATGAGCGTCTCCATCGCCGGCATGCCGGCTTCGCCGAGCTTGAACTGCGCTCTCTGCTGGATGCCTTCCATTTTGGCTCCCGGGGTGGAGGTCAGCTTGTCGAAGCCGGCGTCGCTCATGCCTTGCTTGGCGAGCAATCCATCCATAGCGCGCAAGAACCCGTCCATGTCGCCCGAAGCGACGGCCTTGCCGGCTCCGCTCTCCTGCAGCTGCTTCTCGGACAGATTAAGCCCTTTCAGCAGTTCCGCAGGATCGCCCGCCATCATGGCGCTCATCGCGCCGGCCGATTCTTCGAGGCTGCTCTGAGGGTTCAGCTTCTGCATCCGCATCGCCATCCGGTTGAGAGCGGCCACCTGCGTCGGGTCGGTCGTCACCTTGAGGAAAGACAGCGCCGTCTGCTGCGCCTCCGCCGGATTCACGTTCGCGCCGAGCGCTTGCCTGCTCACCGCATCGAAGATCGCTTGGCCGCCGGCGTCGCTGCCTGCCGCCACCGAGTAGCGGTCGATCGTCTCCTGCTGCACCATCGCGCCCCCGACGGAGCTTTTGAACAACGGCACCGCTGCTCGGAATGCCGCCGTCAGGCCGCTTGTCATCAGCTGAGCGACGCTCGGTGCTCCCTCTCCGGCCTGCGACGCTCCTGCCGCGGCCGCGCCAGCCGCTCCTCCCAGCACGCCGGCGCCCAGAGCGCCCGCTCCGGCAGCTCCGGCTCCAGCGGCGCCAAGCCCAAGCAGCGCCTTCAGCCCGCCCGCACGGAAGGCCAGGAACATTTTCGTAAGCTCCGGGAGCGCTTTAAGGAAGTCCTTAGCGCCAGCGACGAACCGAAAAATGCTCGTAACGCGGTCCATTTTGCCGAATCCACCGCCTGGATCCCTCTGCGCTCCATCCCCCGCCGCCTTCACGCTCACCTTGAACGGCTCGTCCAGCCGCTTCTGAATCTGCTTGCGCAGCCGGCTGATGTCCTCCTCCGGCACGTTCAGGCGGACCTGCAGCGCGAGGCGGGACTGCCGGAGCCGTCCGAGCCGCTGCATCACGCCATTGATCTCCTGATGCGCGCCGCTCGTCTGCACCGACACCTTGAGCGGCTTCGCCAGCTGGCGCTGCAGCTTGTCGCTCAGCTGAATCGTGCGCTCCAGCGTCTGATTCACCTTGCGCAGCTCGCCGCTGAAGCGGTCATACAGCCGGATCGTCGCTTGCAAAGTCGCCATCGCTTCACCCCCTCCTTTCCGTCATCGGCGCTTGCCGCTCCGCGAGGACTGGAGCCGCGCCTGCTTCTCGGCCTCCAGCCGCACGCGGATCATGCCGATCAGCGCGGCCTTGCGCCGCGTTCCCAGCTCTGCGAATTCCCATGGCAGCACCCCGTATTCATTGAGAGCGAAGTACGCATAATTCCACTCGCCTTCCCCCTCCTCTAGTCGTTTTTTACTTCTTCGGCCAGCTCGCCGACCTCGCGGTCGAAGCCGTTGATCTCCTGCACCTTGGCCGCCAGGTTGGCGAACTCGCCCGCCAGCAGCATCTTGCGCACGACGGCCGCCGCGCCGCGCACGCCGTACGACTGCTGCAGCTCGGCGTCATTGAGATCCGGATGCACGACGCAAGCCGCGACCATGCGGCCGAGATAAGCGTTGTAGTCCATCTCCGGCATCGCCTGGCCGCCCTTTCCCTTCGTCCGCTTCATCGACGCGGAGCGCAGCTCCTCGTTCAGCTCCTCCGAGATGGCCCGCAGCTTCCAGGCGGCGGGCCGGCCCGACTCGTCGCGGAATCGGTCCGAGACGACGACCTCCTGCGTTTCGGCGGCGACGGCATTGTGGGCAAAAAACAGCTTCATGGACATGAACAGTTCCTCCTTGGAATGGAAAATCGAATGAAGCGGGAGCGTCCGTGACGGACGCTCCCGGCAAATGACCGCGAATGAGGCCGGCGGATCGGCGGGACGCTTGCTCTGCCTGGAGTCGGCTCGTCGCGCCCGATCAGCCCAGTCCCTGGATGTCCTTGAACGGCTCGCCGATGTTGACGTCATGGAACGTGAACGGAATTTCCTCGTCCAGCGCATCCGACTCCGCGTCGAGCGCGGCCATGACGACCTCGTCGAGATTGACGCCGATCAGCGTGACGATCTGCTTGCCGACAGCCGAGGCCGGATCGTCGTTGGTCACCTGGATGTCGAAATAGGTGTCCACGCCGGTCTTGATGTAATCGCGCATCATCTCGCGGAAGCGGGACGTCACGTAATACAGCGTCATCGTGCCGGTGCCTTCCCAGCCGGCCGCTTTTTTCTGCACGTTGCGGCTGCCGAGCGTCTTGATGTCGGCCTTGTTCTTTTTCGCGGTTGCCCGCAGGTTCTTCACATAGAACATCTCCACCGTCTGTCCGCCAATCGTCGCATAGGCCGTCCCGGAGTGCCCGGCAATCGTGTCTCCCGCTTTCAGTACGCTCATTTAGCTCACCTGTACTTTCATGTAGATTTTTTCGATCGCATCGACCGGCTGCACGGATACGGATACGACAACCGCGTCCGCCTCCGCTCCCTGCTCCACCGTCACGTCCTTGGAGGCGTCGAAGTTCTGCAGCGCCCCCAGCTCCTGGTACTGCTCCAGCAGCTTCACGCAGTCCTTGCGGAACAGCGCGCGGCCGTTCGCATCGTTGCCGACCTTGCCGATATACAGGCTCTCGAAGGTCGCCTTGAAGTCCGTCGCGATCCCGTCGAGCACACGCAGCGCAGAGTTTTTGGCGAAAATGCGGCCCTTCTGCGGCGTCGGACTATGATAGGAGTTGATGTCCTGCTCGACGACGACCGAGCCGGAGCGGGCCGTGAAGACGAACTCGCCGCCGAGCAGCGCCGCCGCCGTAGCCGAGTTCGTCAGGCGCGGAGACGCGTCGCTCGCGCCTTCATAAACGGCGTAGGTCAGCGATGCGGCCGGACCGGCCGCCGCTGTCGCCGCCGCGACCCAGACCGCCGCCTGTCCTGGCGTCAGCGTCTTGCCGTCCTCCAGCGTGACGCCGTTGCGCACGCTGATGACGCCCTCATGATTGGCCGAAGCGTAGTTTTCCAGCACGACCTGGATCTTGCGTCCCTCCTCCTCGCGCAGCCGCGCGGCGAACGCCGCGAACAGGCTTTTCATCGTGACATCCGTCCCCGGATACACCGCCACATGGAAGTCCTGCAGCTCGATCGCCTGCAGGAACCCGGCATAATCCTCGTTCGTCGCCGCGCCGTCCGTACCGCCCGCAAGCGGAACGCCTGCCGTGGCTTCGAGGGCTCCCGAGCCCGTCCAGACGATCCACGCGTTCGCCTTCAGGCCTTGTGCGTTCAGCACGATCTGGCGATCGACCTCCGAGCCGCCGACAAACGTCGCGACTTCCATCTGGCCCGGCTTGTCCACGCTCGCCTCGACCGAGACGCGCAGATCATTGCCGCGCACGCCCGGATAGCGGGCTTCGGCGGTGACGCCGCCAAGCGTCGCCTTGGCCGCCGTTCCACCATTGATGCGGTAGACGAGCAGCTTGCCCGCGCGCTTCATCGCCTCGCGCACCAGTAGCAGCTCCGGCGCGCTCAGCGCGTAGCCGAGCTTCTCCAGCGGATTCTCGCCGCCCTCCAGCACCGTAATCCGCCGCGGCTCTCCCCACGACAGCGGCAGCGGCAGCGCCAGCGTGCCCCTATCGCCCGTCGTCACCGCCGTGCCTTCCGTCGCAAAATTGATGTAGACCCCCGGACGTACCTTGTTCATTGCCGTAAACATGCCTCCAGCCATTTAGTCGGCCTCCTTTTTAATGAATGCTTGAATGCGCCGTTCGACTTCCTCATGCCCGCAGCGCTCTTCGTCGCCGACCAGCACGGAAATCAAGTCCTTGCTGGCGCCGTACCTGCGGCTCCCCAGCAGCGCCGCCTTCGTGAAGCGCGGCTCCAGGCTCGCCTGCTGCTGCTGCTGCTGCGGCTTGACGTCCGCACGGGACGCGTCAGCCGTTTTTTCCGCCTTTTTCCTAAATGCCATTCGGCTCGACCTCCTTGCGCAAGCTCCGCATGAGCGGCGGACGATCCGTCTCATCCGCTCCGTCCAGGCGTACGCTCCAAGTAAAAACGAACTTGCCCTCGGCCAGCTCACGGCTTACGGCGGAGCCCTTGGCGAACCGCCCGTCCGCCAGCGGCACCGACGCCAGCAGCGGCAGCAGCCGCTCCGCGACGAGGTCGGCCCGCTCCGCGGACCGGCAAATCAGCGCCAGTCGACACGCCTCTCGCCAGCGGCCGCCGAGCAGCCGCTGCCGTTCGACCGCCAGCTCCACCAGCTCCAGGCTCGGCTGCGCAGGCGGGGGCTCCGACTGACCGACGGACACGGCGTAATCCGGGAACGCCGCTCTCAGCCGGTCCAGCAGCACGTCGATCCAGCTTTCGCTCATCGGCTTGCTCCTTTCCCGGAGAGCAGCGTCTCGAGCACGCTCTCCAGCCGCCGGGGCCAGTCCCGCTCCAGCTCCGCCAGCGCGAGCGCCAGCATGAAGCGCCCCCGCTGTCCGCCTTCGCCCTCCGTCCCGTACTCGAGACGGGCGGCTTCCGGCGCCGGGTGGCTGATCTCCACCGACAGCACCCGGCTCGCGCGCTTCACTGGTCCGACGCGCCAGCCCTTCGCCAGCTCGCCGCTTCCCGGCGGCATTCGAGCCGCTGCGGATCGAGCCGCGGCTTCCGCCTGCTCCAGCAGATGCCGCTCCAGCACGATCGGCGCCCGCTTTTCCAGCTCCCTCAGCTTGCGCAGCAGCTGGTCCGGATCGTCCAGCTTCCAAGCTGCGATTCCTCCCATGCCAGCTCCTCCTTCCTTCTCTTGCTTCCCGCCGTTTCTCGTGCAGACCGATCGTCAGCTCTCCTCTCGGCCTCTTCTCCTCCGACAGGCACAGGAACGACAAAAGCCGCCCGGTTAGGGGCGGCTCGTCTCTTGTCATCGTTCCTGATACTAGCATCTTACCACGGTCAAAACGGCCTCAGCGGCTCAACTCCGTCTCTTTCGCGTCTCCACTCCGTCTCATTGGAGTCTCACCGGGGGAGGCTGATCTTCTCGCGTCGTTTCGGCGCATGAAAAAGGACGGAGCGCTTTTTCGCTCCGTCCTTTTCTCCATCCTATGCTGCCGCCGCTTGGCGGTCCTCTATCCATCCCGCTGCCATTCCAGAATCCGCAGGAACAACCGGGCCGCCTGCGGCTTCCAGCGGAAGAACGTCGGGCGGGAGATGCAAAGCGCCATCGCGCAAGCCTCGGCTGTCCGCTTCTCGACGTAGTAAAGCCGGATGAGGCTGCCGTACCCTTCCTGCTGCTCCTCCGCGAGCCGCATCGTTTCTTCCAGCTGCTCCAGCTCGGCCTGCAGCCGCTGCAGCTTCGCCATCCGCTCCAGCACGGCATCATAATCGCCGATCCGCCCCGCGCGAGCCTCGATCACCTTCTCCAGCTTGCCTCTGAGCTCCCGCAGCAGCCGGTCGTCCTCGAGATCATTCCCTCTCGTCGGGATCGCCGCCAGCTGCGCTTTCGTGCCGACCGGATGCTTGTCCGGATCGAGGTACGCATTTGCGATCGTCTCCAGCTTCTGCTCCCGAGCGTTCAGATACATATAAGAAGGCATCCCTTTCAGACGGCGGTGAAGGTCCTGCAGCTGGTCCTCCTGATTGAGGCGGCTGACGGTCATTCCGGCTCCGATCGAATAGCTGCCGAGCACCTTCACCTGTATCTTCAGCTCTCGCCAGCGGCGGCATTCGTCGCGGACGAGGCTTTCCAGCTGCCGATTGTCCAGCTCGTCCAGCAGCTCATCGAGCGGTCTCCGTCCCCGTTCCGCTTCAGCGCGATTTTCGAGTCGTTCCATTCTTTCCAAGCCCCTTTCCGTTGACTCAAATTTAATTTGAGTTCAAGCCATTGAAATTCCTTTTTTCAACCCCTTGTTGTCTATCAGCCTATTTCAAGGTATAATGCATCCATAAAGACGAATTTCCTTTGAGCATCCTTGCGGAATACTAGCATAACACCCAAATTATATTTGAGCAAGAGGGAAATGGAAAAGGGAGGAAGGACCGCCATGTCGCTCGGCAAACGAATTCGGGAATACCGGGTCAAACGAGGCTTGACCCAGATGCAGCTCGCGACGAAGCTCCAAATGTCGGAAGCGAACATATCCAGCTACGAACGGGACAAAAGCGCCCCGCCGAGCGACAAGCTCAGCCAGCTGGCGGAGCTGCTCGGCGTCTCCTCGGATTATTTGCTCGCCGGCTCGGTTGCCGCCTCCCCGAGCCTTCAGAAACTGGAGCTGGAGCTGTCGGAGGAGCAGATCCTGACGCTGGCCGCGCATCGGATCGGCCATGAAGGGCCGCTGACCGGCCAGGAGCTGGAGCAGATCAAGCTTGCGCTGCGCATCGCCCTGGCCAAGCCGTAACGAACGACACGAGGACCCGTTTAGGAGAGAGGTTATGTCCAAATATGAACGCCTGCTGAAGCAGACGCCCATCCTTCTTCGCGAGGACGCCGACTTGCCTGAACCGATCAAGGGGCTGTATATGGAGACGCGCGCCGTCCAGGCGATCCTGCTCAGCCGCAGCCTGCGCACGTCGGCCGACAAGGCGTGCATTCTCGCCGAGGAGCTCGGGCACTACCATACGACTGCGGGCGACATCACCGACCAGTCCATCATTGCCAACCGCAAGCAGGAGAAGCTGGCGCGCAACTGGGGCTATGAGAAGCTCGTCCCGCTGTCGGAGCTGATCGGCGCTTATCTCGCCGGCTGCCGCAACGCGTTTGAGATCGCCGACTACCTGGAGGTGACCGAGGCGTTCCTGCAGGAGTCGATCGTCCACTATCAGGAGAAGTACGGCCAGATGGTCGTCCTCGACCGGTTCACGCTTTATTTCGATCCGCTCGGCGTCGTAGAGATGTTCGAGCGCTGA

Protein sequences of DBSCAN-SWA_6

>NZ_CP045802|4288697:4359054|4288697_4289384_-|WP_153784043.1|protease|DBSCAN-SWA
MKKGWIAVLALAAVLAAGPYAAGTTQAERQAPLAADDSYRLASSAVFYLRALGADGTVGATGTGVLLSARGDAATAYHVVKGAAKLEAVLADGKTVSPVKVVRYDERTDAAVLELPAPKSGGGYPFVARRAEKLEHGDAVYAIGYPLKQTPIVTQGIVSSPDAVVSGRSRVLIDAAIASGMSGGPLLDEQGRLAGIISGSLRTMAGIHLAVGMADLNALLPDGLRTAD
>NZ_CP045802|4288697:4359054|4320497_4321664_+|WP_028599120.1|DBSCAN-SWA
MEYELPYGFSAELTARKPVLAILTMSDPKLGFRGNRANFADLVRTGKEMGFIVYVLPMRYLKFSQPMLTGFSLADSAGKGGEWEKGLFPFPDLVYNRIPQREDELMPRVQRKLKLLLASPRVKGVFNPSFFNKWELFEWLRKSQATKRYIPATRRMATVGGLDRMMSKHPYLYLKPVSGKAGKGIMTIRVYPEKPLPYRLSIQNRKKSSTYNCSTVTKLWARILKESGGATYIAQQGIDLALYQERRFDLRALVQKNGAGQWSVTGVGARVAGSKSITTHVPRGGSIEDPEKLLSHAFGAEKARQLISRARSACVQLARQIESASGHSHGEMSMDLGVDAAGGLWFFEANSKPMKFDEPHIRKKSLERIFHYGSYLMRSPKPGKAGGA
>NZ_CP045802|4288697:4359054|4305904_4311172_-|WP_153784046.1|DBSCAN-SWA
MLLRKKGKRGLGLLLAASLLAGAASGGWVKPAEAAAADIEVKQKFGNRIGNLSYGAENAFGNFYNNMESGFYMEHDSATSADWGAGDVFTVNSGATYTLRVGENPLLSAMAQSGHATFKIGFAVLRKHYGVFSGTENSSITVTVNGRQLMDYDTDDTSGSTQIYNKSEQETLTPGAVIRIRVSGEDDDNGPTGVRGLYILFEDKQRPVLEDYTFTGNGATRLNTEINQTELYVKKNEFVDLAYNFSEPIRPTAVSAGFSDYFLRHPLFVNQANTGLPAEGQQQYLQNTTYSAANLGTYHDRLAYRYVASAYHNSGNLPLEPRVDTSTLNALPMDLSLKEKLEQAVLADAAGNVASMRFPNKASAGSLPVVVSAGRAVDPFDYKSGGYRVIVDAVRPKYTKSGNGIQPEILTGTTLNKGDVIDFSVQLTEPGIVNRLWEGQENGTYLLFNNGMRAYYVSGYSKSVWKFRATIGDSVDLETPLLKVVSLSHDRKTPQTSDLEVIQDYAGNLLIQPANFQDTYANAPLDLEPSLVSSKIDWANLMIDNTKPIIGYRYEQGGATGSTYAKEGKMTIDANDPSLLVPPLDPSVPDRGLERPSRGIYRPSNMSAEASPSIGLVYYTWSQSPADPLAGKESDHFAAIKRYSLSAKQPAEELYPEMAGLTLSVTNNKTNLIAPPPEALLPENSGKWYLHAWTADMTWDTARELMQYDKSKDYVAQHPQQYEAWKAEAPGESEADKTVYADNKALQAVGQYGDSKLWELEDFKHDDSNWTHEVGILRLDNKQPVLQPAAVSADGTANVTVEALVEEPHSGIRSIGYQWVKEGFDPQELEWKPATTVAGAVYGDDAPSYTVTQSTYSDVFEDGAYWLYLRAEDQAGNFVVDTPQSAPITVSSEQAVPTKFLPEPKVSFVRSSELTFHIGEALPDSLGYAWSDSPLRPADGAFSPLDPLGTDELGWTSYTIPDEGKSGVRYVHVKAQLGDRTQYYSRAYYFDNEPPQIGFGLEGLSYPLPIQSVLVTVAELYSKNNLNAWFQWVREGESEPTEGSGGWQELKSDRVAQLDGAERLAPGETADFRLYVKAVDGAGNSALAATSGTFKLAGPVKDAPAAPGTSKLISLTGDEEDGYTAIVKLGLQTENPSGYDYSVSPDGGSTWLKWRPYTTFASLKVPSGDPAALQVQVKYRSPGGKVGAVYPVDAAGFDPDAEPVYAVATIPSLTPVNAQTGATIEIAPPPGIRIVPSKLNHVQPVRSGNRFNVKENGFYTFDLSDLNDAKRKETLVVVVNHVDGTPPAGIIQYSVSNNVQTNGSVTAMLTGTEPIVVTNNGGKSAYTFTDNGSFTFTFKDAAGNTGEATAVVANIDRTPPRVKIERSYAYGKDGSLTFGTITDGSGNVVLSSGVTLSVVKADAGARDFVVHSQNNGVAVTQNGVVSFTVGDALGNTLVVKEQVDGIASEGPQPERVSYTFIDANGAELPASRIATIGGKKYAAGRMKVTVSGKIAAPNAVFSGLRPIGTPGAYSNQVSDAGGAYSYSRIFETNGVSSISISDALGNATQIPVTVAGLDNAAPTLRLKQSSVGIVQNKAGFNAAADLGGYEASDNVSAADKIKVEISGLDLGQLGRQRVAYTATDEVGNRTVAYQDVVVVKNGGLLIFGNGTLLSASSGEQALFDTNRITFRVSGYGDMKVGGKAAVNEAGTFELLYQPGLYREGQMKSIATKLTYEQLAGSGFTVTFPKAGWYTVIVRTQERDREYASFFVGSVK
>NZ_CP045802|4288697:4359054|4313177_4316210_-|WP_153784048.1|DBSCAN-SWA
MGIVVLFGIWLPLGIFSERWGGQQPFRAEQGVIDLAGWDGSGRIALDGEWEFYWNELLQPGETPRGERSWMEVPGVWSGSRAAGAERPVYGAATYRLRLTHLSEPGVYRIKKMNIRFASAIYVDGRLVLEDGKPALSAEAYVPGNSPGLAVVEIKGSEAEIIVHAANYDYIDAGVPMSLYFGKEEAINAAHERSLIRESAMAVVLAVIGLIHLVLFAAVWLYGQRDEPLLLFGLTCVTMAVFNGLLGERPLALLLDGLSFQTLYTIKDMSALAGFLVSLYLMMLLQGKGADRRLTKLFALLLLGSLVMFPFLSIREYLSLYRVTILLEHVLMARVLWSAAARHVAAPRGQRYESLLLLLAVLLLNLYSYGCLLFGMSMLGSLLISQIYLILFSLVVFLVIVYRFYGAFRDMERMHRKLLRLDRQKDEFLSSTTYQLKAPLQDIVHLADSLAHAGGPAPGSARSLALIAGTGRRLGYLVQDLHDFSRLKHEDIVPEPRNLDLRSAVGSVLELHRFLLSGRPIELANGVPETLAAVYADEDRLEQILHRLVERAALRAEEGRIEVTAEEELGFAVVTVDFDGRPRPAPDPDVAPCLAAADGEAADLALSITRRLIELQGGLALQPLPGKEGRSFRFSLLLEKNPAASRKAAWPAAGEAAAASETPVALAGGSKGQTVVLVAEPDAASRHAVCQLLAQEGLRAVSVRSAEQARAALALEGELSLVLLGVSLADGSGFDALEQLRNRFSPSELPVLMLTGRRREEERRLALDLGANDYISKPFEAEELLARVRSLVKLRQSVREAREREIAFLRSQINPHFLYNALGAIAELCVEEPEKAERLTLHLSGYLRGSFDFGQRDGMSTLGAELRLIEAYTEIEKARFGSRLQVTLRCEADPALRFPPLLLQPLVENAIRHGLLSRPQGGEVKVTVVEREGYVHAAVEDDGAGFDAQAMLFRLEQPERIGGVGLWNVSERLRLLYGERLGMDSRTGFGSRLTFRIPASSRTSEPKEGG
>NZ_CP045802|4288697:4359054|4324748_4325441_-|WP_153784054.1|DBSCAN-SWA
MTEQAAGNVRLERPEVILFDMDGTLLQTETLLMEAHGRIFAALREEGLYAEPEPPVEALLGCLGMLLEDIWLKLMPTASEAARERANELLLQFELEELAAGKGVLYEGVPETLAELRARGIRLFVASNGLQPYVEGIVRHKRLEPLFDGLYTAGGRGTATKAELVRLLLAEHGVARAWMVGDRSSDVDAGKRNGLPVVGCDYADFGASSELDGADVRIRRFGELLELLGE
>NZ_CP045802|4288697:4359054|4354117_4354585_-|WP_101807993.1|tail|DBSCAN-SWA
MSVLKAGDTIAGHSGTAYATIGGQTVEMFYVKNLRATAKKNKADIKTLGSRNVQKKAAGWEGTGTMTLYYVTSRFREMMRDYIKTGVDTYFDIQVTNDDPASAVGKQIVTLIGVNLDEVVMAALDAESDALDEEIPFTFHDVNIGEPFKDIQGLG
>NZ_CP045802|4288697:4359054|4330476_4331508_-|WP_028599127.1|DBSCAN-SWA
MPIKTLVFIAVGLLLLYLSFTVGAPFLLALVVAIFLEPLNRLLMRKAGMSRLAAAAASSTLFTVLLLALAAGIGFKLAAELIAFWNRAPAMVADANVFFREKFEHAKDVYMTIPPETAVQLEKVLNGLASSLTGMATALSGSVVAVASGLPGMFIFTIVFLVAVYMFSFGLDTMRASFLSLFHEDSQPQLGQVLDNLKDSIFGFLRSQLLLSLVTYVLTLIGLASMGIDYAMAIALLVVVVDILPILGTGSVLVPWAAYMLLAGHSGTAFGLVLLFLVITVVRRIIEPKILGDSVGIGAISALISLYVGFKLVGVIGVFLGPLVVIIYMAARKAGLFQLKIRL
>NZ_CP045802|4288697:4359054|4344889_4346524_-|WP_153784064.1|DBSCAN-SWA
MAKTDWKFNDVVTEADLNALGGEVNAASAHAAVVEGAHGATSAASPGKLMQRDSAGRVKVAAPAAADDAARKAEVDAVQSSLTAHASSQASHVSTADRAKWNGGAGSGLNADMVDGYHFDQDVRKSAIPSFDSINTTQGTSSGGNVHLAMKNNGNIYGGIGLDGASSAGNGGGNLSFWTYDNNGAFITKGLDIARSTGNVTIPKKLNLGGGSNSNFNLADSPIYFRGQNATDGKHYAVYENIGSTDGIRMVGNNTIRLGTFYDTINWTPILTLSGPSASNGTAVQIERHGHAKAANSAPAFPPAGITPASSIVNWQDHPAAVGLIVASRYMADSNAILDVGTVGGGVWQPFFKVTGLGNARVSGTLAVGFNGGSGRNNMNSQAALDLSIGDHDTGLLWNGDNSISMYAAGQQSAYWDALGVRVQKSFSVAGTKSAVVSTSTYGDQYLFAIESPENRFEDYGEAMTDQEGQVIVSMDPIFLETVEIKGEDYHVFIQSIDEGAFYVPERYTDRFMVKGKPNSRFMYRIAAWRRGYHSLRFNHAQGF
>NZ_CP045802|4288697:4359054|4357277_4357898_-|WP_153784769.1|DBSCAN-SWA
MESLVRDECRRWRELKIQVKVLGSYSIGAGMTVSRLNQEDQLQDLHRRLKGMPSYMYLNAREQKLETIANAYLDPDKHPVGTKAQLAAIPTRGNDLEDDRLLRELRGKLEKVIEARAGRIGDYDAVLERMAKLQRLQAELEQLEETMRLAEEQQEGYGSLIRLYYVEKRTAEACAMALCISRPTFFRWKPQAARLFLRILEWQRDG
>NZ_CP045802|4288697:4359054|4328473_4328686_-|WP_153784056.1|DBSCAN-SWA
MDDRRGAAERPPGPAERHAALAAEPGCSRACSRPCPRREARARAEAAERAPQAAGHGREQQSRMDASEGG
>NZ_CP045802|4288697:4359054|4348821_4349118_-|WP_153784068.1|DBSCAN-SWA
MSINDSIKQIMARSLEAQQLTKAVFGKVTGLEPLEVAVEQRFTLPAELLVVPEHLRELAVELGGERVVLRRGLELGDRLVLLRSEGGSPYVALGRVEA
>NZ_CP045802|4288697:4359054|4346526_4346811_-|WP_153784065.1|DBSCAN-SWA
MMEASLIQDVAAYVDGRIARVSLNGGAVLLTEFTLKRASQGVVELRYYIPAEAVGTVHRIELQDASGKTLSVSEVQIPIASDTLMLQSITVEEG
>NZ_CP045802|4288697:4359054|4298250_4305873_-|WP_153784045.1|DBSCAN-SWA
MKLLKRGLSSLLAFVLVFPALFESGHAVAAELGKSRTTTIQNDYIKVTVDNETGRYGIRTIEGQPIRKQDQNVSLLFRGDDPETSFTTFRIDGTDYIFGNKYKFGSEQSRTTEPTLVEKPNGTKQLEMVWSMKGVSIKQILLLYTDGKDKINSGNVNIRYEVTNGSGAKVEVGSRILLDTMVGGNDGPAFQVGTASKAPLLVERRLTHEPEKIGIPPEDAPLHKLPAYWVMRDKLHLENPQATNVVAYGFNNVAEQNINIVDEMVVGHWNGLANTKWDYEVHPNLDFTRDTNDYGSADSAVAFYWNPDAIDPGRMQSFETIYGLGEIVAPDKVFSIRYVDPVQQLATLPDASGYRDEGVFDIIAEVENLPSFNMEHSRLELEMTLESGLSFVQLDEQGNIKRDGSGKPLVDTVSSKRVEYRKEATPEEAKLGIQPKYKPGDTVTATFKVMAKGRPWPTTRQYMLTARSPETRSKIEGIADESIQAQYESVKTNFILLPPVGQATPTYVYGVSPKELYRTDVKYMTVNLSNIEAYTTGGGGTEPNFDLFLVEKSTRERYRVPVADSVLLQPTDDGLTGDMRITYRGGDKVDEAGSVIEEGLGPELPLGEYEIVIDYKGTAGDDPDLASMYDIASGQTILVTDNDESRIREAGILALYKEVVDLSGIDNGATVGEERLEQLNSLFPGEPFEEGSFLYEAATQYKKTRALIGAASKAVDPEFELSEFADEAALSETPLYNYQIFESEEDLEAFEEQAEEDEIERETLVVVRGMVKQVGSGDDQQIIVDTKTEPAIINGAVAYSGKDLVLVRGKLDILGIKQPEGLPLLDTLFVKGDGTLSVASSGFIFHKGEWTLDFFNGFDKTLGGDGYGIPRAGSGEDEEEDEEEESQDANKQSATNPEDDSQNGSLKWAVGGVGDRLNPLRQIMLENVYFNKHSLFSAPSFSIDGFGLSLNDFILREGGISFGGSISLKIVNAEINNVIFNDKGFVGIDAKLGFDLNESLGLFGPKEDKKSGEEGPKKPSGSIGVTHYVQKVDGISNTYGLEFEAQLKNMTEVAIEFSLKQVDDGRILPDVIAFGTQLKSPGILITGATYLTAIRGAVRELADTIAGGTAEDPFPLTIQAGVGVRFGMAPAYFFGDIDLTLKRTGIKIEGVMDYSPDANAEKDDRIEMITMALLEAQWVTPWFVRVQAEVDIGGWDIIVGKAGIFVGQNLEKNRTDFEGYIGSKVQIPGSVPVVGGMPLASVFLGVNNDKLWGSVGILFISLGITYYWGGGVEFGTSTDQLPEGLAHLVIEDPERGPRLLVIGSGVQALADSRVAAEQETQAIEYREIGNGMKIVDNGDMTLGLGGITVKNGGRVHEIPLGGVSGNAIIEVEYDSKEMPAFTLKDGSGKPYPIKFDNTNTDKTANAFTQVVSAKNTGTDVDSRKAYVIIPAAKAAAGGTWTLTAQAPVETKLLNVPTAPQLSEVGLTADPADENKFAATWKVDNAKPGDTVSLYLAKDAVTDATETLASGDVVRKAGDAGMLIAKDLPAAAGRASIDVRRIELAGGTEDIRGLLRQGSYYVRAELKSENAFATKTSAQRFELKDPMAPGKVSDVAVKPAGNGYFHLSFKPGAVKSGQQAYERSYVVEAFQNGIAYEPFGDVLMTEEELQPYWNAASGKYEGIPIGGWAAVSASDQIDTSGLGGTQLVGEEGKEAPKVSHAGLETGRMYVIGVSASAVPTEADDKNRNPHYADRADTAATLLPLVQKPQLTLGGGPVRTSEPGKTFWTYLTSGTEQTISLHSAQPNVEVEAYVGEEYLGKADMRSEGGISRGSLKLTRFATDGTFAVELRSRNTATGDVSVTMLYLTVDTIAPVLYIDEPATGARTQAGRVRVAGSTTPGDVLTVAGQPVEVEEDGRFGGEVLLPEDAGASAELKFVARDAAGNENSAVVDVTNDGYRAPSAIVLKPIPTLRPGDSVKLQAVLQVADGKDGSGKTRYKEVALTEAERERLTLTVDGDSALLAEDGTLTALGAGASLITAEYRVSDGMTLQAMAVAEAKLPQPTSLGALGAEAEAVLGATDKTRVVMTDAGDMTGQQLAYRVYSAGAKLPAFQEDLSTWSLLPADGIVAAKYGDTVVVAKRLSSGKLAMAAKLLPASIWMMMPGGFGFGGGGGAPAGDKPQASVNGAAIEAAWEGKTALIRLDGSVLEGGVAADLTLRSAEAGAEGYRVTVERALADKLAAAGKTLRIELPMASLALGAPQLRGGKDDLVLAFGLNDSGERTLLDAAAAAQGFQLLGGGAGSKLQLGLEPAGWKPAPSATLPLPEGVRTKDVTAVLLRAADGSWTPLPWKPAAGGAAALVRLTGSGSVYFAASTRTFTDVAPLFWAADSIRQASARMLVLGQSADKFAPNAKVTRAEYPTILLRAAGYMNEPAAAVRFGDVPADSWYARTVGIAVGLGLASGKSAERYDPNAALTRLEAMAMAGRLMAIAQPGAQLEEAEIARVLGAFADVKAIPDWARGPVAAAVKAGLIQGIDGSIRPGDPLTRSQAAAIAVRASDWMNS
>NZ_CP045802|4288697:4359054|4331605_4332955_-|WP_153784057.1|DBSCAN-SWA
MTTEFHPGDIALNLLVVVVLVLLNGFFVAAEFALVKVRTTRLTQLASEGSKKAGYALRIAHRLDAYLSATQLGITLASLGLGWVGEPAISHLIAEPLLHRIGIADETVVSTVSIVIGFLVITFLHIVIGELAPKSLAIQKSEGVSLWLSAPLLFFYAIFKPAILLLNGAANRLLRLIGIEPASEHESAHTEEEIRLLVNQSAQSGIIDDNEMKLVGNVFDFGDLLAREVMLPRTDMDCLFTTRSLEENREMVYRTRHTRYPVAIEEKDQIIGFVHIADLLTADRGSVPDLRKLIRPVLNVPESMEVSQVLQLMQARHSQLAVVVDEYGGTAGMLTAELILEEIVGKIHDEFDEAPPAITVQGEATTVDGRMLIDDINRLLQLDLEDEEVDSIGGWMFRRLGGTPEQGKKIGYREYTFEVAECQPLRVLRVRIYRNPEAAADRDEPAEES
>NZ_CP045802|4288697:4359054|4342886_4343888_-|WP_153784062.1|DBSCAN-SWA
MIDLGYPIERRYIRIRPQTRPGLRLTAGSPAFFVAHDTGNPGATAEAHYRYFDRQTERTASAHVFIDDTRILEIIPTGTGDDPAEKAYHVQRQAPEDNRRFGADANDAALGIELCYGGAIRFEAAYDRYVAYLAYCCAKWSKVPSTHIVSHGQLDPTRKRDCEQALATAGRTLADLIRDVERKLAAAVQAEESSARPAEPSSAGSSGRNQAGAAADSAKTQQDGATAASSPAALSAATCSHLVRSYIQPAWHERIQAGDSEGAAHYARLAERLRRCVDGERLLKSNAQEIIVGWLSPAWFKTRAKGENPDRFRAMADELRRCAAIPPSGSALW
>NZ_CP045802|4288697:4359054|4321665_4322586_+|WP_153784052.1|DBSCAN-SWA
MKAMLLTPKQWTRSREPLLRLMAAWGGGRLSAAGLAALKELRAEELEPAGGGAPAAALAVLLEQGRPAGIAFARKAGREACLVAVSPPCRGRGAGSRLLRELQRTWGALDCRVAADNAASMKMCFRAGMAAVALEDGPTGKPTLVFRSGASALAAQGAQDGAARAEALREAGRIETAQVNAARSQAGRSEVERFEVERPQAERFETAWFEAAQPQAERSQVGRSEAERSEAAWPQAERSQVGRSQVGRSQVGRSEAGATRAARTAGAARTPSSRPSGRELLPKKPAAARRDDHGSAGARHLNVIPQ
>NZ_CP045802|4288697:4359054|4329658_4330387_+|WP_043111400.1|DBSCAN-SWA
MFDSDITERFVAYSPAHLISLGLIFAAVLLLFAFRGPLARRRPASGRYALAGLLAACEILLNVWYVSNGVFRPEATLPLELCSISLYLSVIMLLLRSRLLFQIVYFTAIGGALQALATPVLGYAFPHFRFLEFFAAHGLLLLAALYMVWVEGFRPTLRSPFIAWGAVNAIAAVVFAVNRLTGANYMFLARKPPSSSLLDYLGPYPWYILSLEAVALLLFLLLYLPFARSGRRGREPARAPSP
>NZ_CP045802|4288697:4359054|4356128_4356542_-|WP_153784074.1|DBSCAN-SWA
MSESWIDVLLDRLRAAFPDYAVSVGQSEPPPAQPSLELVELAVERQRLLGGRWREACRLALICRSAERADLVAERLLPLLASVPLADGRFAKGSAVSRELAEGKFVFTWSVRLDGADETDRPPLMRSLRKEVEPNGI
>NZ_CP045802|4288697:4359054|4325437_4327342_-|WP_153784055.1|DBSCAN-SWA
MPHGRGDSAMDRELREEMDLALLWDKVEEAVYVLDPEWRFIYANRMTEQFAGKPREQLIGTLLWDLFPANWVERAKPVFEQAAATGRSARFEEYSPESDRWYAVQALPLPPGLAVVLREITAERKNSQRLDQRYESLFRQNQDSVFQMDLEGRFVLVNPAMAAITGYSERELIGSSFEPLLHPDELPEAREHFRLAAAGQPQYREYRIINSQGHELYGQVTKFPIVVDGHVIGIFGMGRDITLQKRSELKIREAERRLRSLIAHHSDAILELDIDGKVRECNPASLKLLGAQPEELAGKRLDELMNLDKERRDELTRLWDGADCHTSPLALPLPLRSGETILAEVEFVPILIHGQRDGAYLILKDLTQKLETEKLLLKSEKLQTAGQLAAAVAHEIRNPLTSLKGFVRLLETYNERPEKAYMFQILQEEISRIDSITNELLMLAKPQKSIVKQVRLDGVLEAVATLMSPQALLKSIELRLEPLPEAVVLGEEYGIKQVFVNLVKNAIEVMEQGEIRIELEAAAEGWHVRVADEGGGMPEECLDRLGEPFYSTKEKGTGLGLMVTKRILEAHDGTIEFRSRRHVGTVVEVYLPRESPLQKRRIAEAGELPGDRLRLAGADRLGYSGKSEERGEPG
>NZ_CP045802|4288697:4359054|4354585_4355899_-|WP_153784072.1|tail|DBSCAN-SWA
MAGGMFTAMNKVRPGVYINFATEGTAVTTGDRGTLALPLPLSWGEPRRITVLEGGENPLEKLGYALSAPELLLVREAMKRAGKLLVYRINGGTAAKATLGGVTAEARYPGVRGNDLRVSVEASVDKPGQMEVATFVGGSEVDRQIVLNAQGLKANAWIVWTGSGALEATAGVPLAGGTDGAATNEDYAGFLQAIELQDFHVAVYPGTDVTMKSLFAAFAARLREEEGRKIQVVLENYASANHEGVISVRNGVTLEDGKTLTPGQAAVWVAAATAAAGPAASLTYAVYEGASDASPRLTNSATAAALLGGEFVFTARSGSVVVEQDINSYHSPTPQKGRIFAKNSALRVLDGIATDFKATFESLYIGKVGNDANGRALFRKDCVKLLEQYQELGALQNFDASKDVTVEQGAEADAVVVSVSVQPVDAIEKIYMKVQVS
>NZ_CP045802|4288697:4359054|4337037_4337529_-|WP_101807984.1|DBSCAN-SWA
MAKEIEIRQQRRGVRAAAPESLSARMMAEQAGAVFPLLERVPDGSGEAFGLIDWHRGWLEQAAAAGREDVVAAPTHVKVVADDRFEAVISWREAAQAAFLFAREGVPLEREGPLRLYVPDGSSKCLNVKRVVSLTLLEEPELGGDAAYGFKSDFSPEDLRKRR
>NZ_CP045802|4288697:4359054|4348453_4348825_-|WP_052333303.1|DBSCAN-SWA
MSVPEQTGLDWTAAEAVERPSLTYPIHLDGRTGGRIDGLAAMRQFVFKQLSTVRWEHEVYTGEVGLERSSYDIAAAVEEALLADSRVLAVEDMQMRREGDGVSLTFTVRTVFGSFKEEAMAGV
>NZ_CP045802|4288697:4359054|4333015_4334146_-|WP_153784058.1|DBSCAN-SWA
MNPEMTLQPLLTPLSPQNDPWDPLGSLERFGRHALTSVEFTVTNLCNMRCEHCAVGDTLTMREPDKLPLELMLSRLDEVEQLQTISITGGEPSYSERTVRDYIVPLLKYARSRGIRSQLNSNVTLDYSRYELIAPYLDVMHISFNYTSADDFHEVGFARSGHSVPRSAAVRMYERMIDNARRLSDAGVLVSAESMINYRTWRKMPEIHRLIREMGCERHEVHPMYPSAWAGGLPALSKEQMRQAVEELLDARDPQLWMLFGTLPFYSCSSDPADRDLLARLGREPNVTVRNDPDGRNRLNVNLFTGEVFVTDFSDIPAFGNVQDERLDDVFARWLDHPLSRSVSCHCPAAACCGPNLLVKQMYYEEVDFMKQKAVL
>NZ_CP045802|4288697:4359054|4312055_4313174_-|WP_153784047.1|DBSCAN-SWA
MLRAIIVDDEELSMRRLARIAGELGGVEIAATFFHPSEACAYVRDHHVDVAFLDINMPEIDGMELGLRLRQLREPLQIVFVSGYDRYAVDAFEQDAVDYVLKPVNAERLAKTLERLSRRARPPQPPPSAPKLGVRMFGGLRFFRTDGPGRETPIKLRSPKTEELFAYLLCKGTASREEVADTLWRGLEPDKAAKNINSTLYYIRKSLAEAGLEPLLLAGRYDIRIDAARVDCDLYEYERLVQRIRAEAAPDARQFDQAEAAAPGGFLQGRLYEWAAELSRRLERERMERLEGKARLLVRDGKPAAAFPLFEQMLELDPLREDIHEELIRHYLFLGRTHDAARQYRELEERLARELGTAPARPFASYVGSAHF
>NZ_CP045802|4288697:4359054|4340629_4341685_+|WP_153784061.1|DBSCAN-SWA
MRVHISDLKEGDLLSSDAFNHFGLNVMAKGTRLTSYEIAKLTQHSIDYVEVEMEAPVAAGYRTIESGLPPRWLPSIKPLYENAISGCENLFRKALEEGKVSEEDVDRSFGPLMSSFQMEKDVVSMLLLLNTDDDYTYQHSVQVGMLSYYLASWLGFPEEEAARIGKAGFLHDIGKCRISKDILNKPEKLTSEEYREIKRHTLYGEEIILSTYDDPFLSSAALQHHERMDGTGYPHGIDGIEISPIAKIVAVADVYSAMISTRSYQQKRDLLYVLRELYRMSFHELDPHTTHTFIRHMIPNFIGKSVELDNGQFGTFIMTHPSEFFRPLIQVGEDFLDLSEQRELEITQIYM
>NZ_CP045802|4288697:4359054|4335534_4336980_-|WP_153784059.1|DBSCAN-SWA
MERSTDNKRSRLLLLHSNDVHSRLEEAGRIAAAVKDARRDEGEQGVLYVDIGDHLDRMRQETEGTGGSVNIALLNAAGCEAAVPGNNEGLTFTRDELERIYAGARFPILCCNLLDARTGERPEWLLAGTVLVKNGLRVALIGATAAYPAFYSLLGWTVTDPLEAVREQVGRLRGAADAVVVLSHLGLPVDRRLAEEIDGIDVILGGHTHHLLEEPERVRGALLCGAGKFGERLGLVELGLDPSSGRLEAAGRLLPIASLPIDEEAAELLSEHGETARRELSRPAATLERPLELDPARESPLANLLAAGVREWTGADIGLVNAGQLLGGLPAGEISEGLLHALCPSPVNPCRMRLIGRRIREAVEQSLQPEFYGKELRGFGFRGTVLGTLAVDGLEIDWSPAADGGGRIVSIRCGGRELEDEREYDVGTLDMFTFGAGYLPLKEGRDVRYFLPEFIRQVLAAELNKPEALRRCGEPRFRLVR
>NZ_CP045802|4288697:4359054|4334296_4335418_-|WP_028599130.1|DBSCAN-SWA
MILMPLSMCRPGMRLAKKVLSGEGLVLLGEGFELTSRLIERLQECQINFLFIQDEATDDILINELISEDTMRVAMTEIRASFRQMMDLPQRRRGAAYPFVGPQLRDVMNRVIDDLSAHKESVVMLMNMASVDNYLYQHSFNVCVYSTMLGIHHGYSRDELTVLGMGALLHDVGKTMVPVELLKKPGLLTREEFEEMKRHTEYGYELLRHEAGVPAAAALCALQHHERLDGSGYPFGLKGKEIHEFSKWIGMVDSYDAMTTNRIYREPMLPHQAVEALYAGTGTQYEQSMVQLFRDKVAIYPVGMTVRLKTGEIGVVVDVRPSCPHRPVVRVLRDDEGVRLRAPYEIDMSLQLTRMIAGVNDELPEAQLAGAPS
>NZ_CP045802|4288697:4359054|4358192_4358546_+|WP_153784076.1|DBSCAN-SWA
MSLGKRIREYRVKRGLTQMQLATKLQMSEANISSYERDKSAPPSDKLSQLAELLGVSSDYLLAGSVAASPSLQKLELELSEEQILTLAAHRIGHEGPLTGQELEQIKLALRIALAKP
>NZ_CP045802|4288697:4359054|4319127_4320498_+|WP_153784051.1|DBSCAN-SWA
MSLTLCNVHFSDKKDRVVYVSGPLYRSLKLSDKKKLQIKLGRETVTASVKAVKREGNHVFLSSALRQQIRVPKSGNVFMLHASENEVQLGPLVGILSDGYVSSSLPFGSRTGFIKDLIRIGEKKAYFFGFTPKDINWPQETVNGYFLNADGSWYRKTVPLPDVVYNRLPSRKAETGSYISSLRERFVRKGIPFFNWSYFNKSDVYKLLDKDVEALRHLPESVSGPSDAKIKELLEKHHFVYFKPSGGSLGAGIYRLTYQPKQGYFARYRSGGKNVLLRFGTFQALMRTMHARHGSSFGGYVVQQGIRLVEIEGCPLDFRFHMHKNGRNEWVTAGIGAKKAGKGSVTTHIKNGGVLMTPGNALSRTFGSQAGEVLEKAKRVAVRMSEAIERNYPHRLGELGLDLGIDKDGEVWMFEANAKPGRSIFKHPALKPEGRASLEYILEHCLYLSRFRGRDS
>NZ_CP045802|4288697:4359054|4341769_4342846_-|WP_101807989.1|DBSCAN-SWA
MTPSSLFLLALFALLVLSLVSARTKTRRSAERPLSSSKNPRRNAVAEAARETAGWLDLGALPDAPLQATAAKLDKALPASYVEQLRQRYLTEHPDCSPERFELLLLELKRYFVLCSLLRTVPMFGDEVDGVWHEMLMYTREYERFGKELIGGPLHHAPAAESVPDPGGRAWFDLAYAALFRFHAFAPVAWGAFFRHPLNAKRLERLQDAEPRELRSELFRPEADERLVSYMLDKLRRQAADAREARSADRSDSPGRLSGSSYADPGYGAMLGGALLMSSMGGSFDEQMERHLPEAERERSQSGCSASGCAGGDSFDERGSGSSDSGGDGSSDGGSSSSCSSSSCSSSSCSSSSCGGGD
>NZ_CP045802|4288697:4359054|4328688_4328970_-|WP_028599124.1|coat|DBSCAN-SWA
MSEEQQKQAFDKEAYQAGLKELQVLDFALVELNLYLNTHPGDLQAIQQFNQLAQKRQAVAQQFELQFGPLVNFGNSYSRYPWQWNETPWPWQV
>NZ_CP045802|4288697:4359054|4358580_4359054_+|WP_153784077.1|DBSCAN-SWA
MSKYERLLKQTPILLREDADLPEPIKGLYMETRAVQAILLSRSLRTSADKACILAEELGHYHTTAGDITDQSIIANRKQEKLARNWGYEKLVPLSELIGAYLAGCRNAFEIADYLEVTEAFLQESIVHYQEKYGQMVVLDRFTLYFDPLGVVEMFER
>NZ_CP045802|4288697:4359054|4343880_4344162_-|WP_101807991.1|DBSCAN-SWA
MDWTLIQSMIHPELAGVVAVCWIIGYGLKRTAGIRDWMIIYFVTAAGIVFAGFTAGWTADGVMQGIFCGAVAVYGNQLVKQTAQALRKEDAHD
>NZ_CP045802|4288697:4359054|4356538_4356937_-|WP_153784075.1|DBSCAN-SWA
MGGIAAWKLDDPDQLLRKLRELEKRAPIVLERHLLEQAEAAARSAAARMPPGSGELAKGWRVGPVKRASRVLSVEISHPAPEAARLEYGTEGEGGQRGRFMLALALAELERDWPRRLESVLETLLSGKGASR
>NZ_CP045802|4288697:4359054|4355899_4356139_-|WP_153784073.1|DBSCAN-SWA
MAFRKKAEKTADASRADVKPQQQQQQASLEPRFTKAALLGSRRYGASKDLISVLVGDEERCGHEEVERRIQAFIKKEAD
>NZ_CP045802|4288697:4359054|4289435_4298168_-|WP_153784044.1|DBSCAN-SWA
MKARKRYRTWRMAALGAVILAGAAGGTAMLAGAGAQTWDGSADTSWFDATYTTFKIDTPAKLAGIAKLVNGENGVDGLKGKILEVDRSLDLSAYDWLPIGTESHPFKGTLIAKDGAMFGISGMRVPAAIPYQGLVGNMDGGTVGGFRFEADGEIDVTVAGNVYAGSAVGKMTGYSIVYDIENELAIEAESGSGVAYAGGIVGSGSGQVSNALNEASVTVAGSTYAGGLVGHVSEGGLTLKKAANDGAVSASGGAASELYAGGLTGLTAGALDMQGESTPIRNGGAVTVSGGRLAHAGGLAGHYGSPVTFSADTANSGEVSVTSPDAEESYAGGVAGSIGGVLPDASVALRQTAAVHHAGGERVYSGTIAGFVGPALTWSKGFEQAIPITAEGKDVYVGGLFGYAAQGVSLTDDDPAAYVSAAAVEAQGTGAVYAGGIVGYNGGGLIRHASFKSGLTADTSGDSAVYAGGIAGYLAAGAEISSSAAGGTAAQPLAIVAEGELGGIAGHSDGTISASSASWLTLRAQRSGSAAGGIAGAASGTIAGARAGDPSASDSASLRFETAIASPAGGRDDFAAGGLIGRGIGELTVSGSRVDRVSAALPAGMTGVAFGGAAGRIDGAAVLGTSAQPLAVRAVTLEAPADEVALGGGIGRLDGSAQASLLVSGFEVDSSGARARIGGIAGENAGSLSGGAAEAVTIRSTGADARLGGAAGLSRGSILGAAARSVALAAGGSGAEAGGLVGRLEGTADSRASLTDSKLEGGESPTAAATAAGARIGGIAGYAVHADLIRPAALAEAPNYVALTLSAPGIEAGGLAGRADSSRIESDLQRVNMQNLLLTASADASQAKAGGLVGSSVETTLRGLVGSGASLLLSGPDTAAGGLAGTLKGGEGAAIVDTVFGGMQLKANASASGSFVGGMAARLEARASDPAAAPASSSGVIVNSRVSGSVQALAPGMTVGGLVGENASLIANVSVTDKIPVSSKGANAVVGGFVGRNAATGTLYYTYTNASLTIEGQGTLAGGLVGDNAGRILASYTDLDLTSKAYGTSGQPVFLGGLAGRSSGTVEQSYAASKVTASGAYAQAGGLLGELAGGSVKNAYSAKSVTASGSGSYAGGFAGRIVSGRISSSYSAAEVSASGTALAGGFAGRYDNASKELLYKSYYIKDEKLNLNKDLPDFADGEYRWLSVLGRLSTILSSTLSDRSEFPALSGWDFAGAWKYGSLGAQYQYPEVNRAASSGGGEEGTGGNVNANLNWYLRDKDATTFQIGTEAELAGLAAIVNGTLVGVEPFSFAGRTIEIKGPIHVQSAQWSPIGVSEALAFQGELLGGGHLIDGYAVSGEVPFGGLFGVIGADGSASGLALEPKEARGSSYAGALVGLNYGRIADIALKLPAGASVSGGVAGGIVGRSEGAADSLRAELAGGRVESAAAGGAAGGIAGENVSAIAAGSWSLTTSGEVGSRIAATGDEAAAGGLAGRQSGTSSALKLELTRLAVEASGIDSAAGGLFGSYADGDASELSVSFGEAVSVSAGADDAAAGGLIGRSAAGNGLSGLKVEAAPSALGVTGGGSAGGLIGEKTGRGIAAWDVRDASVQGLAVKAPAGSDEAAVGGLIGRADQTALGGVKASFASLDARGEAVYAGGIVGRAAETTIQDAEASGPIAAALDAGSVGALAAGGIAGELSASDRDAGLRFGGLYPLYRGLYQAEYEGELHLAAAGGESALHAGGLVGALRSASIYDSSSRAHIAAGSAGELDAGGIAGFSSGILVHADAFGGIDASGSGVYRVGGLVGRALDGEIHYSRAVAAGGSRIAVGTALTIGENLPATFVGGALGQGDRLVVARSSASIPVDVADGNIDTTLYAGGFAGQLGENGAGSGSIRYAYADGAVTAAGKRGSYAGGFAGSINRFAVEDSYASGSVSNTGQDTRTGGFAAAVERSGSVLRSHALQERVATTGLAGTTRSYTGGFAGYNDGKIEQAYASAIELTVSAKGTDTHKGALVGYNFRDGRIALSAYSGSGAAVGRNAGAAASAEAVPARDPRPAGSWAATYDPSVLLLSADGEIAIGSRAQLDGYVRLSNDTGAAYFKLFDRAATASPLGSGDKLRLTADIDLSAFGWTPLQAFDGELAGDGHRLIGLRADGGSGDAALALVNRGRIADLQLVGASVQAGRHAGLVAAINADGGDIRGVTAEGKASGGAGAGLIAGVNESGGMLRDVTAEGSASGADAGLVAGINAAGGDIRGATAEGSASGRLSAGLIVGDNAGLIAESGAAGLARSEASAGGIAGINRQDGVIERSYSAADASSKGAEAAAGGAAGRNDGRISDTLASGRATADGTALAWAGGLAGRSAGAVERSVAGGEAVASIQGALVPGRSFFGGLAGQLADGGKIAGASFHRQLVKRGVAYYDAAGIIRTEGGLDGAALTSGTLPSGLSGGVWRAAAGFYPAPSDSPLARLAAAAVMPAAGDTINRLTAGFGLSRADGLLWSADPSLVQLHSGSGRLLADGVAELQASLGGFARTIVLNAPELRWPQAAAAPQVVSGDREFKEKVEIDLSAEPGAVIHYTLDGSEPSEQSAVYSSPILLKATTTLKAIAVVLGKEHSPALSGEWKLQPPSSPSGGGGFFFPAPSPSPTPEPKPAVESNIGKPAIGDEQPAAVRAPRGSILRLTAPEGKWIRYTTDGSDPTESSPRFTGELVLNRSVTVKALVEGDKRILTYKFDVGAAQYSLRKDASTVRYASGYADGMFKPDAAMSRYELIEALAPLLDREEGELYNAFPDKSGRSDQLVAFFASAGIVGGYPDGTFGGDRGLTRAEFAVIAARALQISVDGDAVPKQKDARKHWASSFIAALTDAGYIQGFPDGSFRPNSPLTRAQAISLLNRMAGTAKRADAGPHYGDVPPSHWAYADIMAAARD
>NZ_CP045802|4288697:4359054|4339489_4340533_+|WP_101807987.1|DBSCAN-SWA
MSEGSRPALPDRYIRQTRFAPIGPDGQQRLGGSVVAVVGVGALGCVIASHLARGGVGELRLIDRDIVELSNLQRQLLYDEDDAASSLPKAEAAAAKLRRANSSVSIRAYAADLHAGNADELLGGTDLILDGTDNFHTRYLLNDYAVRAGIPWIYGGAVGAGGMTMSVLPDAGPCYRCLFPEPPASGLADTCETAGVVSPLVDVIGSLQAMEAIKWLSGRREEMRGDLLQLDLWRNSWMPLGVAGARRSDCECCGRREFPFLEPEEDMAAALCGRATVQIRPARSRPLDLPALAERLAMAGEVRLTPYSLRYERDERISVVFFPDSRALIQGLEDPIKAKAVYADILG
>NZ_CP045802|4288697:4359054|4317932_4319087_+|WP_153784050.1|DBSCAN-SWA
MKSDAGVIGVWIGKAPRPDGSGRLTVPEDGFLAALAERAAELRLPLHLFAAEGFRAETGSLTGYVREGGCWQEREVALPAVVYDRCGPSGASSRRSSELQLERMRRLHPHARLSSWLPGKLAQLEALRRAGSELAALAPPTRLLNGASSVAEAAREWGAVFLKPDGGMQGRGVLSLGPDGSGWLLRGRAGDGRTLAARLPDLEAAAERTERLVRGRRYILQPQLPLCDRQGRPFDVRALVQKDGRGRWRLTGTALRRGRPGGIASNLHGGGEALPARDGLELLLGAEGAARCSAEIDRLALLAAEAAENAFGRLAELGLDFGVEPDGRLWLLELNSRPGRDAFSSFPGGIARTAVERPLLYARLLGARPVPERSGARSSAAPSR
>NZ_CP045802|4288697:4359054|4316486_4317863_+|WP_153784049.1|DBSCAN-SWA
MLKSKSKIAVQVTQGGHGADDAIVLGESVLKHHKIPSGTPIALRFGSYRTAVRVVSGGKGDTMRLPSALARSLGIHGAVSLRLHFRPSTQTLSLGPLIGVLVSRDYPQQPDRPFGSITMFCRELVDACAAQGAHVYFFTPEAAGPGPRIDGWVHGDGGWRKASLPVPDVVNNRLTARKLENRPSVQQLFREAKSRYGTQVFNEKFLDKHEVFDALGKDPSLGKYLPESRLLKSFADLKTVSSRHATVFLKPVRGSLGKGIIKASRMEGEGILATYTAPTGIRRQAYPTLAKFYGSLGGKMKTVRYQLQQGLTLIDIGKRPVDFRALVQRSGTGAWIVTSVVARTAGSNHFVSNLARGGTLSRVKDAVGRSSLAPGYKAGASAKLEKAALDIAKGIEERIPAHFGELGIDLAMDTGGRVWLLEVNSKPSKNDNTPLEGGKIRPSVRNMIQYARYLAGFQ
>NZ_CP045802|4288697:4359054|4347384_4348461_-|WP_153784067.1|tail|DBSCAN-SWA
MYEHQTYREIMGRMLARIPDELDKREGSVIFDALAPAAAELAALYAELDVQLALSFADTADGEYLTRRAAEHGVRRKASSRAMRLGRFFGAAGGPAEVPLRSRLAAEGTAYEVAERLAPGTYRLVAELPGRAGNEVAGALLPLDYIDGLARAELADVLVPGEDEEGDAELRARFWQAVSEQPFGGNIADYRAKIGGLPGVGGVKIHPAWNGGGTVKATVIASDFAPAAAALVQEVQAAIDPESAGQGIGLAPIGHRVTIVAADAVPVDIATQLTLRAGVSAVQLERDIEAAAEAYLLELRRAWAGESRLIVRISQLETRVLALPGVEDIGGTTLNGAPANLELEADEVPTLGTVTLNG
>NZ_CP045802|4288697:4359054|4327899_4328469_-|WP_028599122.1|DBSCAN-SWA
MWLYEKKLQYPVKVSKCDPMMAKFLVEQYGGADGELAAALRYLNQRYTIPDKVIGVLNDIGTEEFAHLEMIATMIYKLTKDATPEQLREAGLGTDFVNHGGDLFYNSAAGVPWTATYIAAKGDPLANLYEDIAAEEKARATYQWLIDYTDDVDLQDSLKFLREREIVHAMRFRESVEIIKADMGQKKIY
>NZ_CP045802|4288697:4359054|4337560_4338556_-|WP_101807985.1|DBSCAN-SWA
MLRDRFGRIHDYLRISVTDRCNLRCLYCMPEEGMEFADSSELLSYDEIVQVVEAAAGLGFRRLRITGGEPLVRPGLDGLIRRLKAIPGIEEISMTTNGMLLAKQAAALKAAGLDRVNISLDTLDAARFRFIARRGGLEQVLAGIRAAGEAGLGPIKLNCVLLKGINEDEIKSFLRLSVEQPLHVRFIEYMPIGHADEQWRRTYLPLTAVMDAARELGLPMAPLEELRGNGPSENWAFEGAAGSFGLIHPVSDRFCARCNRLRLTADGSLQPCLYWVDELNVKPALGSRAALEALFRRAADIKPENHEMAARLHGEALSHSPTSRRMSQIGG
>NZ_CP045802|4288697:4359054|4322542_4324318_+|WP_153784053.1|DBSCAN-SWA
MAQPVLGILTLYLNENKALEERPIYQRMIVAGKKMGLDVFVFTPADVDYEKNRIQAMIYDPSSKTWSRRWTSFPHMIFDRCRIQQSYRFEQLQKFRSRYGHLTFLNRMLRNKWTVYKTLAAQSRFQGRQPLTVLYAGHKDLADMLRRFPLVFLKPINGTGGRGILRIERQKEGVYLIQGRDQSRRIIRPQKVGAAALQERLSSWSLGGGKYIVQQGIMIKLPSGRVHDYRLLVQKNGRGEWEPTGCAGRVGAAGSITSNLHGGGKAMRMEELLSSWVGDEELAASVRREAEQFGVEVAAHLERQYGRLCELALDLAIDKKGGIWLLEVNPKPAREVFRQSGDLATYERAIVKPLEYALYLYSRRGRKSGGRTTGGRTAGSRTRGSRTAGSRTTGSRTTGSSLGGAQPVGSGPAADEAATLGSGSKRRNAEPGGSRSPAGTAAGSGRSGLAGSAAGSGSSGPAGSAAGSGKSGAASAAADGGKRSAAGGAQGRVSKQPPGGRRGENESPNRRRKPRPLAGSGPFAANKPTIRSVPAPASSALSADMDEAELEPLAAPADTAAKQADPSVKQADPSAEQVDTAAAPQTEENGE
>NZ_CP045802|4288697:4359054|4349121_4350114_-|WP_153784069.1|DBSCAN-SWA
MLKIELDLRDGRLWDVTGMATELSWKTSRIGKAGTLEFSMMRGPSLAAQSQLPIAPGNVVRVSDGGVRLFYGYVFTLEEDEDRVVRVKAQDQLRYLLETDTYVRTNVTATQVIRDQALAIQARLGPIADTGHPIPKFSQDGQKRLDMIFKALDETLLAKGKLFVFYDDAGLLTLRDVADMKASVVIGENSLLTGYSSSRSIDSETYNRIKLVRDNKQTGGRDVYIEQDGAAIARWGQLQYYQKVDEGLNEERIKEMLKQLLQLKNREQRKFSLEALGHPTIRAGSVVQVTIPRLQLNRNFLVEECTHAYSGRSHTMQLELYVIDGMVKEG
>NZ_CP045802|4288697:4359054|4344542_4344869_-|WP_153784063.1|DBSCAN-SWA
MGKKIKLLAVTQNFDMEGNVSQFRVSYQVIESGSILLSNAMLVLPLNDELDLSDSLALSPNTFNGYTDGIRKIGESNVLSYYSILLNYLTTKIKIKEGVDEGLVPSGV
>NZ_CP045802|4288697:4359054|4338683_4339493_+|WP_153784060.1|DBSCAN-SWA
MSYSWSIALFAGLPERLGTRQAELSSDRSEMTVGELKAALSEAYPAHAGLIAVCFAARNEAYAADGELVRCGDELALLPPVSGGDGSGAPIAAAAACRICAEPLDAAAVASLVEHPDHGAAIVFIGTTREWTAGQRTVKLEYEAYEPMALRTLEQIRRELDERWPGTRCAIHHRIGVVGIGEASVVIAVSGPHRAAAYEASRYAIERLKQIVPIWKKEVWEDGSEWKGHQTGPWNPLSDLAPPVPPAASDKLPAEEAAAAVGAERELSE
>NZ_CP045802|4288697:4359054|4328979_4329195_-|WP_028599125.1|coat|DBSCAN-SWA
MPGAGYREWLPFRGACDPCPPIGVRRYVIPPNQYILYQPTGLPQYPLEEALRLGTLWPALYSPYEPGCGRS
>NZ_CP045802|4288697:4359054|4353558_4353981_-|WP_043111402.1|portal|DBSCAN-SWA
MSMKLFFAHNAVAAETQEVVVSDRFRDESGRPAAWKLRAISEELNEELRSASMKRTKGKGGQAMPEMDYNAYLGRMVAACVVHPDLNDAELQQSYGVRGAAAVVRKMLLAGEFANLAAKVQEINGFDREVGELAEEVKND
>NZ_CP045802|4288697:4359054|4350898_4353355_-|WP_153784071.1|DBSCAN-SWA
MATLQATIRLYDRFSGELRKVNQTLERTIQLSDKLQRQLAKPLKVSVQTSGAHQEINGVMQRLGRLRQSRLALQVRLNVPEEDISRLRKQIQKRLDEPFKVSVKAAGDGAQRDPGGGFGKMDRVTSIFRFVAGAKDFLKALPELTKMFLAFRAGGLKALLGLGAAGAGAAGAGALGAGVLGGAAGAAAAGASQAGEGAPSVAQLMTSGLTAAFRAAVPLFKSSVGGAMVQQETIDRYSVAAGSDAGGQAIFDAVSRQALGANVNPAEAQQTALSFLKVTTDPTQVAALNRMAMRMQKLNPQSSLEESAGAMSAMMAGDPAELLKGLNLSEKQLQESGAGKAVASGDMDGFLRAMDGLLAKQGMSDAGFDKLTSTPGAKMEGIQQRAQFKLGEAGMPAMETLIPVLDKIMAVFDSGKLDPFFDALSAGLYIMAELLSAAADAALFLINLFVSNGDAIGDVLTVLTAVLLPLMAVWLWSMVAPIMAMAAAFFMANWPLLLIIAIIGLLVYALLQTGTSAGEIIGFIVGLFFFLGATIYNMIASAWNLFATFAEFLINLFIDPVYAVQKLFYDLAMMFGNALYEMLLMTESFAGGFMKIILEGINGVIGLVNGLGAGMAKLFGKEYKGIAELDVKDPHALSSKLKGMLDKIEPPTSEKDPVRIGRLDALDPSAAGKKGYDLGKGALDKAGSLFNGEKDPLKEMFKGENKLGGGGGMADKQNSMMGGAGAGAAPGGNIPNIGKVNEVGSIGSEVDIGSEELKVMRDLAEMKAIQNFVTLTPTVQVTTGPIHKQVDVDDVVRKIAASMEQEIESSAHGVYARI
>NZ_CP045802|4288697:4359054|4346807_4347392_-|WP_153784066.1|DBSCAN-SWA
MAEPLIGRLPAFYSDSREMTELFRSEDEEIASAEQALERLLDDRFVLTASVEAIRRHERLLGIRADEAQESLAFRRVRVVNRYSTKPPFTLRYLQERLDDLVGKGRALAQVDLEAQVLTISAAIQNAPLFREVEQTVTALKPASLVYVQQTAVADTLRLREGIRYRRLARETRLGSWKLGATGFTTEKEEVIVR
>NZ_CP045802|4288697:4359054|4350118_4350856_-|WP_153784070.1|DBSCAN-SWA
MAIPIRVSPQPAKAFAGIRLDFNHGTEGWELPVLPSKLSIRRSGSGKDYNLLGAGPIATIEKPGLAEVEFESFFPSQPGPYVATRSILKRPEQFADDIGRWMRSGYPLRFIYARHADRFENPYTLQIPMTITGFDRWEEAGSPGDVFYTLKLKEYVFYAPVKLQAVKTADGSTAVAKEPDKRPDLKVPPKAYTIVKGDTLSGISMKLYDGDSSRWPEIQKLNGIGNSELKRLQIGRVLQVPPPKE
>NZ_CP045802|4288697:4359054|4344186_4344501_-|WP_028599139.1|DBSCAN-SWA
MSRPENQLQAIVSQVVKLETLQEVNTRALGELASGVARLIERLEKSDETAREAAQRARAAHHRIDEIRASIDGIKQGQRWLITTSFTLIGLAASLLGLVFKILE

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_153784043.1|4288697_4289384_-|protease	trypsin-like serine protease	NA	NA	NA	NA
WP_153784044.1|4289435_4298168_-	hypothetical protein	NA	NA	NA	NA
WP_153784045.1|4298250_4305873_-	hypothetical protein	NA	NA	NA	NA
WP_153784046.1|4305904_4311172_-	hypothetical protein	NA	NA	NA	NA
WP_153784047.1|4312055_4313174_-	response regulator	NA	NA	NA	NA
WP_153784048.1|4313177_4316210_-	response regulator	Q9EYF3	Enterobacteria_phage	3.6e-19	36.6
WP_153784049.1|4316486_4317863_+	YheC/YheD family protein	NA	NA	NA	NA
WP_153784050.1|4317932_4319087_+	YheC/YheD family protein	NA	NA	NA	NA
WP_153784051.1|4319127_4320498_+	YheC/YheD family protein	NA	NA	NA	NA
WP_028599120.1|4320497_4321664_+	YheC/YheD family protein	NA	NA	NA	NA
WP_153784052.1|4321665_4322586_+	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_153784053.1|4322542_4324318_+	YheC/YheD family protein	NA	NA	NA	NA
WP_153784054.1|4324748_4325441_-	HAD hydrolase-like protein	NA	NA	NA	NA
WP_153784055.1|4325437_4327342_-	PAS domain S-box protein	NA	NA	NA	NA
WP_028599122.1|4327899_4328469_-	hypothetical protein	NA	NA	NA	NA
WP_153784056.1|4328473_4328686_-	hypothetical protein	NA	NA	NA	NA
WP_028599124.1|4328688_4328970_-|coat	spore coat protein CotJB	NA	NA	NA	NA
WP_028599125.1|4328979_4329195_-|coat	spore coat associated protein CotJA	NA	NA	NA	NA
WP_043111400.1|4329658_4330387_+	TIGR02206 family membrane protein	NA	NA	NA	NA
WP_028599127.1|4330476_4331508_-	sporulation integral membrane protein YtvI	NA	NA	NA	NA
WP_153784057.1|4331605_4332955_-	DUF21 domain-containing protein	NA	NA	NA	NA
WP_153784058.1|4333015_4334146_-	radical SAM/CxCxxxxC motif protein YfkAB	NA	NA	NA	NA
WP_028599130.1|4334296_4335418_-	HD-GYP domain-containing protein	NA	NA	NA	NA
WP_153784059.1|4335534_4336980_-	bifunctional metallophosphatase/5'-nucleotidase	NA	NA	NA	NA
WP_101807984.1|4337037_4337529_-	hypothetical protein	NA	NA	NA	NA
WP_101807985.1|4337560_4338556_-	GTP 3',8-cyclase MoaA	NA	NA	NA	NA
WP_153784060.1|4338683_4339493_+	molybdopterin converting factor	NA	NA	NA	NA
WP_101807987.1|4339489_4340533_+	thiamine biosynthesis protein ThiF	NA	NA	NA	NA
WP_153784061.1|4340629_4341685_+	HD domain-containing protein	NA	NA	NA	NA
WP_101807989.1|4341769_4342846_-	hypothetical protein	NA	NA	NA	NA
WP_153784062.1|4342886_4343888_-	N-acetylmuramoyl-L-alanine amidase	D6QWN1	uncultured_phage	9.5e-33	48.3
WP_101807991.1|4343880_4344162_-	hypothetical protein	A0A0A7RUL4	Clostridium_phage	1.4e-05	42.4
WP_028599139.1|4344186_4344501_-	hypothetical protein	NA	NA	NA	NA
WP_153784063.1|4344542_4344869_-	hypothetical protein	NA	NA	NA	NA
WP_153784064.1|4344889_4346524_-	hypothetical protein	NA	NA	NA	NA
WP_153784065.1|4346526_4346811_-	ketopantoate hydroxymethyltransferase	NA	NA	NA	NA
WP_153784066.1|4346807_4347392_-	DUF2313 domain-containing protein	A0A0K2CNM8	Brevibacillus_phage	3.9e-31	42.4
WP_153784067.1|4347384_4348461_-|tail	phage tail protein	S5MUH6	Brevibacillus_phage	9.7e-84	47.7
WP_052333303.1|4348453_4348825_-	DUF2634 domain-containing protein	S6B9X2	Thermus_phage	2.0e-12	37.7
WP_153784068.1|4348821_4349118_-	DUF2577 domain-containing protein	S5MC71	Brevibacillus_phage	1.3e-09	34.5
WP_153784069.1|4349121_4350114_-	hypothetical protein	S5MA66	Brevibacillus_phage	5.6e-78	45.0
WP_153784070.1|4350118_4350856_-	LysM peptidoglycan-binding domain-containing protein	S6BFJ4	Thermus_phage	1.5e-30	34.6
WP_153784071.1|4350898_4353355_-	hypothetical protein	S5MNW9	Brevibacillus_phage	5.5e-74	35.3
WP_043111402.1|4353558_4353981_-|portal	phage portal protein	Q708L8	Streptococcus_phage	6.8e-17	37.4
WP_101807993.1|4354117_4354585_-|tail	phage tail tube protein	S5MA61	Brevibacillus_phage	1.3e-40	55.2
WP_153784072.1|4354585_4355899_-|tail	phage tail sheath protein	A0A0K2CNL4	Brevibacillus_phage	2.8e-101	45.6
WP_153784073.1|4355899_4356139_-	hypothetical protein	NA	NA	NA	NA
WP_153784074.1|4356128_4356542_-	hypothetical protein	NA	NA	NA	NA
WP_153784075.1|4356538_4356937_-	hypothetical protein	NA	NA	NA	NA
WP_153784769.1|4357277_4357898_-	RNA polymerase subunit sigma-24	NA	NA	NA	NA
WP_153784076.1|4358192_4358546_+	helix-turn-helix domain-containing protein	R9VW28	Paenibacillus_phage	1.6e-11	57.6
WP_153784077.1|4358580_4359054_+	ImmA/IrrE family metallo-endopeptidase	A0A0K2CZC9	Paenibacillus_phage	1.7e-32	48.7

Sequences of DBSCAN-SWA_7

Nucleotide sequences of DBSCAN-SWA_7

>NZ_CP045802|4966897:4976580|DBSCAN-SWA
GCTACTTGTCCGCCGAATCGTCGTCCGCTCCGGCTCCTGCGTCGGCGGAGACGAGCGCGCGGCGGCCGTCAAGCGAGATCCGCCCCTCGGCGAAGCCGCGCACCGCCCACGGGTAGAGCGCGTTCTCGGCGGCGTGGATGCGCTCGGCGAGCGAGGCCTCGCTCTCGCCCTCGCCGATCTCCAGCGCCCGCTGCGCGATGATCGGTCCGCTGTCGAGGCCGCCGTCGACGAAATGGATCGTGACGCCGGTCACCTTGACGCCATAGTTCAGCGCCTGCCGGATCGCATGCATGCCGGGGAATGCCGGCAGCAGCGACGGGTGGATGTTGATCATCCGCCCGGCGTAGGCGTCGACGAGCACCGGCGTCAGGATGCGCATGTAGCCCGCCAGCACGACGAGGCCGACGCCCCGCCGCTGCAGCTCGGCGAGGATCTCGCCTTCGTAGGCCTCGCGCGAGGCGTACGCCTTTGGATCGAACACCCAGGCGTCGATGCCGGCGCGTCGGGCGCGCCCGACGACGGGCGCCTCCGCCCGGTCGCAGACGAGAAGCTCGATGGAGCCTCCGAGCTTCCCGTCCGCCGCCGCGTCCGCCAGCGCCTGGAAGTTGCTGCCCTGGCCGGAGGCGAAGACGGCGACGCGCAGCTGCCCGCCCGTCCGGTCTCCGTCCCCTAGATCGAAGCGCAGCTGCTCGGCCATCAGACGTCCGCCCCCGTGAAGGTGACGATGCGGCTGCCCTCCGTGACGGCGCCGATGCGGTACGCCTGCTCGCCGAGCTCCGCGAGCGCGGCGAGCGCCGCTTCCGCCTCGTCCGCCGGCACGACGACGACGAGGCCGATGCCCATGTTGAACGTCGTGAACATGTCGCGGTTCGTGATCGAGCCTTTGTCCTGCAGCAGCTTGAAGATCGGCTGGATCGGCCAGCTGCCGAAGGCCACCTCGACGTTCACGCCTTCGGGCAGCACGCGAGGGATGTTCTCGATGAAGCCGCCGCCGGTGATGTGGGCCATGCCCTTCACCTGCACCTTGCCGATCAGCTCCAGCGCCGGCTTGACGTAGATGCGCGTCGGCTCGAGCAGCACGTCGCCGAGGCGCTTGCCGCCGAGCTCCGCCAGCTCGTCCTGCAGGCCGTAGCCGGCCTGCTCCAGCAGCAGGCGCCGCACGAGCGAGTAGCCGTTGCTGTGGATGCCGCTCGACGCCAGGCCGATGACCGCGTCGCCCGGAGCGATCGCGCTGCCGTCGATCATCTTGGCGCGGTCGACGACGCCGACCGTGAAGCCGCCGATGTCATACTCCTCCGGCGTGTACATGCCCGGCATCTCGGCCGTCTCGCCGCCGATCAGGGCGCAGCCCGCCTGCACGCAGCCTTCGGCGATGCCGGCCACGATCTGCTCGATCTTCTCCGGCTCGACCTTGCCCGTCGCCAGGTAGTCGAGGAAGAACAGCGGCTCCGCGCCCTGCACGATGATGTCGTTGACGCACATCGCGACGGCGTCGATGCCGATCGTGTCATGCTTGTCCATGGCAAAGGCGAGCATGAGCTTCGTGCCGACGCCGTCCGTGCCCGAAACAAGCACCGGCTCCTCGTACTTGTTCTTGTCCAGGCTGAACAGGCCGCCGAAGCCGCCCAGCCCGCCGAGCACCTCCGGACGGATCGTCCTCTTCACATGCTTCTTCATGCGCTCGACCGCTTCGTTGCCCGCTGCGATGTCGACGCCGGCTTGCTTGTATGCCTCTGCCATTCACCTGTCACTCCCTGCAATTTGATCTTCTAGCAGCTGCAGCTCTTGTCCGAGCTTTCGTCGACCGGGGTCGGGTAGTCGTTGTTGAAGCAGGCGAGGCACAGGCCTCCGCCCTTGCTGTCGCCCGGCACCGAGGCGGACTCGATGAGCCCCTCGGCGCTCAGGAAGTAGAGCGAGTCGGCGTTGATCGCCTCGCGGATCTCCTCGACCGTCTTGGACGAGGCGATCAGCTCGCGCCGGTCCGGCGTGTCGATGCCGTAGTAGCACGGGTTGGCGAACGGCGGCGAGCTGATGCGCACATGCACCTCGGCCGCGCCGGCCTCGCGCAGCATGTTGACGATGCGCAGGCTCGTCGTGCCGCGCACGATCGAGTCGTCGATCATGACGACGCGCTTGCCCTGCACGATCTTGCGCACGGCCGACAGCTTCATCTTGACGCCTTTCTCGCGCAGCTCCTGGGAGGGCTGGATGAACGTGCGGCCGGAGTACTTGTTCTTGATGAGCCCCATCTCGTACGGAATGCCCGTCTGCTCGGCGTAGCCGATGGCCGCGCTGATGCTGGAGTCCGGCACGCCGACGACGATGTCCGCGTCCACGAACGCCTCGACCGCGAGGCGGCGTCCCATCTGCTTGCGGGCCGTGTGGATGTTGACCTCGTTGATGTCGCTGTCCGGCCGGGCGAAGTAGATGTACTCCATCGCGCAGCTGGCGCGGCGCTCCTCCTCGTCGAAGCGCTCCTCGCGCAGGCCGTCCGCGTCGAGGATGAGCAGCTCGCCGGGCTGCACGTCGCGCACGTACTCGGCCCCGATCGTCTCGAACGCGCAGGTCTCGGAGGCGAACACGTAGCCGTCGCCGAGCCGGCCCATGACGAGCGGACGCAGGCCGTTCGTGTCGGAGGCGACGAGCAGCCGCTCGTTGGTCATGATGAGGAAGGCGAAGCCGCCGACGATGCGCCGCAGCGCGTCCCGGGCCGCGCTCACGAAGTCCTTGGGCGAGCGCGCGATCAGATGGGCGATGACCTCGGTGTCGCTCGTCGTCTGGAAGATCGAGCCCATGCTCTCCAGCTCGCGGCGGATCGACGGCGCGTTGACGATGTTGCCGTTGGTCGCCACGGCCAGGTCGCCGTCGCGGTACTTGAACACAAGCGGCTGCGCGTTGCCGAGCTGGCTCGCGCCGGACGTCGAGTAGCGCACATGCCCGATCGCGCGGTCGCCCGGCAGCGAGGCGAGGATGTCGCTCGTGAACACTTCCTTGACGAGGCCCATGCCGCGGTGGTAGGCGAAGCCGCCGGTCGCGCTGTCCACCGTGCAGACGCCCGAGCTTTCCTCGCCGCGATGCTGCAGCGCGTGCAGGCCGTAGTACGCCAGCGACGAGGCGTCCGGCGTGCCGAACACGCCGAACACGCCGCATTCTTCCTTGAGCTTGTCGAAAATATCGTCGCGGCCGATGCCCGCGTTGTAATGGGCGTCCTCCCAGGCGCGCGACACCGCGCGCAGCTCCTCGGAGCCGGGGCCGGCGAAGCGTCCCCCGGCGGCAAGCGCCGGAGGCGCCTCGCCGGAGGCCGCCGTGCCGTCAGCATGGAGGGCGGGGGCGCTGCCTGCGCCCTCGCCCCAGCGGGAGCCGGACTGAACCTCCAGGCCTGCTACTTCATGAGGCATGGGATCGCTTCCTTCCACACGCTCCGCAGCTCCGACACCGCCGCGCGCACGCCCGGCCGGCCGTTCACCCGGATGTCCAGCTCCTCCCCGCCGACCGTGCCGAGCTCCGCATGCGGCACGCCGCGCTCCGCGAGCAGCGCCAGCAGCTCGCCCTTGCGCTCCGGCGATGCGCTCAGCAGGATGCGCGACTGCGACTCGCTGAACAGCGCGTGGTCGGCGCGCAGCTCCGTCGCGACGTCCACGCTCGCGCCGAGGCCGCGGCCGAAGCTCGCTTCCGCCAGCGCCGCCGCCAGGCCGCCCTCGGACAGGTCATGCGCGGAGGCGACGAGGCCGGCGCGGATCGCCGCCTGGACTGCGTCCAGCAGCGTCTTTTCGACCGCCAGGTCAAGCGCCGGGGGACGCCCCTCCGCCTTGCCGCCGCGCACCTGCTGCAGCTCGCTGCCGCCGAATTCGGCGCGCGTCTCGCCGAGCAGGATGATCGCGTCGCCGGCCTGCTTGAACTCCTGCGTCGTGATGTAGTCGATGTCGTCGATCAGGCCGACCATGCCGATGACCGGCGTCGGGTAGATCGCGCCTTTGGCGTTCTCGTTGTACAGGCTGACGTTGCCGCCGATGACCGGCGTCTCCAGCACGCGGCACGCCTCGCTCATGCCGTCCGCCGCCTTTTCGAGCTGCCAGAACACCTCCGGCTTTTCCGGGCTGCCGAAGTTGAGGTTGTCCGTGATCGCCAGCGGCTGCGCGCCGGAGCAGACGATGTTGCGCGCCGCCTCGGCGACCGCGATCGCGCCGCCGACCTCGGGATCGAGGTAGACGTAGCGGCCGTTGCAGTCGGTCGTCATCGCCAGCGCCTTGCGCGTGCCCGGCACGAGCACGACGGCCGCGTCCGAGCCCGGAGGCACCGCGGTGCCCGTGCGCACCATGTAGTCGTATTGACGGTACACCCATTCCTTGCTCGCGACCGTCGGGGAGCCCAGCACGTCCTTGAGCGCGCCCGTCAGATCCGTGATCTCCTCGAAAGCGGCCGTGTCGATCGACGCGCTCGCCGCATAGGAGGCCGGCTCCTGCGAAGGCTTGCTGTATACCGGGCACTCGTCCACGAGCGCCTTGACCGGCATGTCGGCGACCTGCTCGCCTTGGTGGAACAGCCGCAGGCGGCCGTCGTCGGTCACCTTGCCGACCTTGGCGCAGATGACGCCCCAGCGCTCGAAAATCTCGCGCGCCTGCGCCTCATGCTCCGGAGCGACGACGAACAGCATGCGCTCCTGCGACTCGGAAAGCATCATCTCGTACGGCGTCATGCCTTCCTCGCGCTGCGGCACCTCGTCGAGGTACAGCTCGAGGCCGTTGCCGGCCTTGGAAGCCATCTCGGCGCTGGAGCAGGTGAGGCCCGCCGCGCCCATGTCCTGGATGCCGAGCACGATGCCGGAGTCGATCAGCTCGAGCGTCGATTCCATGACGAGCTTTTCCATGAACGGGTCGCCGACCTGTACAGCCGTGCGCTTCTCCTCGGACTCCTCGGACAGCTCGACCGACGCGAACGTCGCGCCGTGGATGCCGTCGCGGCCTGTCGCCGGACCGACGTAGAACACCGGGTTGCCGACGCCCTTGGCGACGCCGCGCTGGATCTTGTCATGGTCGATCAGGCCGACGCACATCGCGTTGACGAGCGGGTTGCCCTCGTAGCTCTCGTCGAACATGACCTCGCCCGCGACCGTCGGGATGCCGATGCAGTTGCCGTAGCCGGCGATGCCGCCGACGACATGCTCGAACAGATACTTGACGCGGTCGCTCTCCAGCCGGCCGAAGCGCAGGCTGTTGAGCAGCGCGACCGGACGCGCTCCCATCGAGAAGATGTCGCGGATGATGCCGCCGACGCCCGTCGCCGCGCCCTGGTAAGGCTCGACCGCGGACGGGTGGTTATGCGACTCGATCTTGAACACGACGGCCTGGTTGTCGCCGATGTCGACGATGCCCGCGCCCTCGCCCGGTCCCATGAGCACCTTCGGGCCGGTGATCGGGAATTTCTTGAGGATCGGCTTGGAGTTCTTGTAGGAGCAGTGCTCCGACCACATGACGCTGAAGACGCCGATCTCGGTGTAGTTGGGCAGGCGGCCCATGAAGCCGCAGATGAGCTCGTACTCGTGGTCCGTCACGCCGAACTGCTGGTAGATCCTCTGCTCGGCGATCTGCTCCGCCGTCGGCTCCAACGCCTTAGCTGTTGACTGCTGCGTCATGCTGTTCCCTCCATGCGTTCAAAATCGATGTGAACATCCGCTTGCCGTCCTCGGAGCCGAGCAGCTGGCTGACCGCCCGCTCGGGATGCGGCATCATGCCGACAACGTTGCCGCGCTCGCTGCAGATGCCGGCGATGTCGTGGACCGAGCCGTTCGGGTTGCCGCCGCTGGCGTAGCGGAACACGATCTGGTTGTTTTTTTGCAGCCGCGCCAGCGTCTCGTCGTCGCAGTAGTAGTTGCCTTCGCCGTGGGCGATCGGGATCGAGATGACCTCGCCCTCGCGGTACTGGTTGGTGAACGGAGTGGCGGCGTTGACGACTTCGAGCGGCGATTGGTGGCAAAGGAACTTGAGGTCGCGGTTGCGCAGCAGCGCGCCCGGCAGCAGGCCGGCCTCGGTCAGGATCTGGAAGCCGTTGCAGATGCCCAGCACGTACTTGCCGGCCTCGGCGGCCTTGACGACCTCGGCCATGACCGGAGCGAAGCGGGCGATCGCGCCGCAGCGCAGGTAGTCGCCGTAGGAGAAGCCGCCCGGCACGAGGATCGCGTCGTAGGCGGAGAGGTCCGTGGCGGTATGCCAGACGTAGTCGACGGACTGCCCGATCGTTTCTTCGACCGCCTTGTAGCAGTCGATGTCGCAGTTCGATCCGGGGAAAACGATGACGGCGAACTTCATCCGATCAGCCCTCCAGCTCGAAGCGGTAGTCTTCCACGACCGTGTTGGCCAGCAGCTTCTCGCACATGGCGCGCACGCGCTCCTCGGCCTCGGCGCGGTCCGTCGTGTCCAGGGTCAGCTCCAGGTACTTGCCGATGCGGACCTTGTCCACTTCCGCGAAGCCCATGCTGTGCAGGGCTCCCTGGACGGCCGTTCCTTGCGGGTCGAGCACGTTTTGCTTGATCGTCACGTATACGGTTGCTTTCATCGTGGCAACTCCTCTTGAGTGGATTGATTATCAAGGCGGTTGAAGATTCGTCGGGCTGAATGTTTGTCGGGTGAAGCTGCTTGCGGGCTGATGGGCGGGCGGCGGAACGATTGGGGCCGCCGGAGCTATCCGCTGACGCCGCTCCGGGGACGGAACCTCTTTCCGATTCCGCTGAAGCCCAGATTCCTCGATCTCCCTTTCCGAAACGTAAGGAATCCGGCCTTCAAGGGAACCGCTGCCGCTTCTCCAAGAGGTTTCCGTCCCCTCCGCTCCCTGCGTAATGCTCACCAGCTCGATTTTTTCGACTTAACGCCTACCGGTCGCGCTCCTCGAAGCTGAGTTACTCGGGTTTTCCGCGCAACTCCCACCGTCGAACGCCTGCTAGTGCCGAGTTACTCGGGTTTTCCGCGCAACTCCGACCGTCGAACGCCTGTTGGTGCCGAGTTACTCGGTTTTTCCGCGCAACTCCGACCGTCGACCGCCTGTTGGTGCTGAGTTACTCGGGTTTTCCGCACAACTCCGACCGCAGACCGCCTGCTGGTGCCGAGTTGCTCAATTGGCGCCCTGCAACCCGATTTTTTCGGGCTGCAGCGCCTGCTTCTGGCCTCCGGGCACCCTGCAACCCGATTTTGTCGGGTTACAGCGCCCGCTTCTGGCCCCCAGGCTCCCGTAACCCGATTTTCTCGGGTTGCAGCGCCTGCCTCAGGCCTCCGAGCATCTGCAACCGGACTTTTCCGGGTTACAGCCTCTGCTTCGAGCCCCCGGGTGCATACAGCCCGATCAAAATCCGGCTGCGGCTCCGCGGAATAGCGGTCAGCTCAGCTCCTCGCCGGTAATGGCGCGGTAGATGGCGCGGTAGCGGGCGGTCGTCGCGGCGACGACCGGCTCCGGCAGCGGCGCCGGCTTGCTGTCCTTGTCCCAGTCGGAGCCGAGCAGATACGTCCGCACCGGCTCTTTGTCCATGCTGTCGATCTCGGTATCGAGCTCGTACTTGTCCTGCGCCCAGAAGCGCGAGCTGTCGGGCGTGAAGATCTCGTCGATCAGGATGATCTCGCCATCGACGAGCCCGAACTCGAACTTGCAGTCGGCCAGCAGAATGCCTTGCTCGAGGCAGCGCGCATGCGCGAACTCGTACAGCGTGAGGCTGCGGTCGCGCAGCTGGGCGGCGACGTCCGCTCCGACCAGCTCCTCCATCCGCGAGAACGGAATGTCCTCGTCGTGGCCGACGTCGTTTTTGGCCGCAGGCGTGAAGATCGGCCGCTCGAAGCGCTCGTTCTTGCGCAGGCCCGCCGGCAGCGGGATGCCGTTGATCTCGCCGGTCGCCGCGTACTGGCGCCAGCCGCCGCCGGTGATGTAGCCGCGCACGACGCATTCGATGTCGATCCGCTCCGCCTTGCGCGTCACCATGATGCGGTCCCGCAGCGCGTCCTTGTCGGAGACGAGCTCGCCCAGTCGCTCCACATCCGTATGGACGACGTGGTTCGGCTGGATCGCGGCCGTCTGTTCGAACCAGTAGGCGCTCAGCCGGTTGAGCACGCTGCCCTTGTCCGGGACGGGCGGATCGAGCACGTAGTCGAACGCGCTGATGCGGTCGGTGACGACGATCAGGTAATGCTCGCCGAGATCGTAGAGCTCTCGGACCTTTCCTTTATAGAGCAGCGGCGCCTGGATGAGGCCTGCCGCCGTCGATAGCGCCTCCGTTGCTGCAGCCATGATGGTTCCTCCTGCCAATGCGAGATGGATGAAGCGAAAACGATGGGTCGCTTGAGCGAGCCTGCAGCCGTCCGAGCGGACGATCCCTAGCGAGCGAACGGTGCCCGCCGCCGCAAAAGCCCCCTAGATCAGCTCCAGCCGGCGGAAGATCGTGTCGACATGCTTGAGATGCCAGCTCGGGTTGAACGCGTCGTCGATCTCCTGCGCGCTCAGCGCGGCCGTGATCTCCGGCGTCTCCGCGATGATGTCGCGGAACTGGCGCTGCTCCTCCCAAGCCTGCATCGCGCGCGGCTGCACGGTGTCGTACGCCTGCTCGCGGCTGAAGCCCTTGTCGATCAGCATCGTCATGACGCGGCCGGAGAACGGCACGCCGAACGTGCGGCCCATGTTGCGCTTCATGTTGTCCGGGAACACCTGCAGGTTCTTGATGATGTTGCCGAGGCGGTTGAGCATGTAGTTGAGCAGCATCGTCGCGTCCGGCAGGATGACGCGCTCCACGGAGGAGTGGCTGATGTCGCGCTCATGCCAGAGCGGCACGTTCTCGTAGGCGCTGATCATGTGGCCGCGGATGACGCGCGCCAGGCCGGAGATGTTCTCGCAGCCGATCGGGTTGCGCTTGTGCGGCATCGCCGACGAGCCCTTCTGGCCCTTGGCGAACGGCTCCTCGACCTCGCGGAACTCGCTCTTCTGCAGCGCGCGGATCTCGGTGGCGAACTTGTCCAGCGAGGTGGCGATCAGCGCCAGCGTCGCCATGTACTCGGCGTGGCGGTCGCGCTGCAGCGTCTGCGTGCTGATCGGCGCGGGCTTCGTGCCGAGCTTGCGGCAGACGAACTCCTCGACGAACGGGTCGATGTTGGCGTACGTGCCGACCGCGCCGGAAATCTTGCCGTACTGGACGCCGTCCGCCGCATGGCGGAAGCGCTCCAGGTTGCGCTTCATCTCCTCGTACCAGAGCGCCAGCTTGAGGCCGAACGTCGTCGGCTCCGCATGCACGCCATGCGTGCGGCCCATCATGACCGTATCCTTGTAGGCGACCGCCTGGCCGCGCAGGATCTCGATGAAATTCACGACGTCGCGCTCGAGGATCTCGTTGGCCTGGCGCAGCAGATAGCCCGTCGCCGTGTCGACGACGTCGGTCGACGTGAGGCCGTAATGCACCCACTTGCGCTCCGGTCCGAGCGTCTCGGACACCGCGCGCGTGAAGGCGATGACGTCATGGCGAGTCTCCAGCTCGATCTCGCTGATCCGGTCGATGTCGAAGCCGGCCTTCTCGCGCAGCGCGGCGACGTCCTCCCGCGGAATGACGCCGAGCTCGGCCCACGCCTCGCAGGCGCAGAGCTCCACCTCCAGCCACGCCTTGAATTTGTTCTCTTCCGTCCAGATCGCCCGCATCTCGGGCCTGCTGTAACGCTCCAGCAT

Protein sequences of DBSCAN-SWA_7

>NZ_CP045802|4966897:4976580|4974261_4975161_-|WP_028598680.1|DBSCAN-SWA
MAAATEALSTAAGLIQAPLLYKGKVRELYDLGEHYLIVVTDRISAFDYVLDPPVPDKGSVLNRLSAYWFEQTAAIQPNHVVHTDVERLGELVSDKDALRDRIMVTRKAERIDIECVVRGYITGGGWRQYAATGEINGIPLPAGLRKNERFERPIFTPAAKNDVGHDEDIPFSRMEELVGADVAAQLRDRSLTLYEFAHARCLEQGILLADCKFEFGLVDGEIILIDEIFTPDSSRFWAQDKYELDTEIDSMDKEPVRTYLLGSDWDKDSKPAPLPEPVVAATTARYRAIYRAITGEELS
>NZ_CP045802|4966897:4976580|4970278_4972528_-|WP_153784291.1|DBSCAN-SWA
MTQQSTAKALEPTAEQIAEQRIYQQFGVTDHEYELICGFMGRLPNYTEIGVFSVMWSEHCSYKNSKPILKKFPITGPKVLMGPGEGAGIVDIGDNQAVVFKIESHNHPSAVEPYQGAATGVGGIIRDIFSMGARPVALLNSLRFGRLESDRVKYLFEHVVGGIAGYGNCIGIPTVAGEVMFDESYEGNPLVNAMCVGLIDHDKIQRGVAKGVGNPVFYVGPATGRDGIHGATFASVELSEESEEKRTAVQVGDPFMEKLVMESTLELIDSGIVLGIQDMGAAGLTCSSAEMASKAGNGLELYLDEVPQREEGMTPYEMMLSESQERMLFVVAPEHEAQAREIFERWGVICAKVGKVTDDGRLRLFHQGEQVADMPVKALVDECPVYSKPSQEPASYAASASIDTAAFEEITDLTGALKDVLGSPTVASKEWVYRQYDYMVRTGTAVPPGSDAAVVLVPGTRKALAMTTDCNGRYVYLDPEVGGAIAVAEAARNIVCSGAQPLAITDNLNFGSPEKPEVFWQLEKAADGMSEACRVLETPVIGGNVSLYNENAKGAIYPTPVIGMVGLIDDIDYITTQEFKQAGDAIILLGETRAEFGGSELQQVRGGKAEGRPPALDLAVEKTLLDAVQAAIRAGLVASAHDLSEGGLAAALAEASFGRGLGASVDVATELRADHALFSESQSRILLSASPERKGELLALLAERGVPHAELGTVGGEELDIRVNGRPGVRAAVSELRSVWKEAIPCLMK
>NZ_CP045802|4966897:4976580|4973205_4973448_-|WP_028598681.1|DBSCAN-SWA
MKATVYVTIKQNVLDPQGTAVQGALHSMGFAEVDKVRIGKYLELTLDTTDRAEAEERVRAMCEKLLANTVVEDYRFELEG
>NZ_CP045802|4966897:4976580|4972505_4973201_-|WP_028598682.1|DBSCAN-SWA
MKFAVIVFPGSNCDIDCYKAVEETIGQSVDYVWHTATDLSAYDAILVPGGFSYGDYLRCGAIARFAPVMAEVVKAAEAGKYVLGICNGFQILTEAGLLPGALLRNRDLKFLCHQSPLEVVNAATPFTNQYREGEVISIPIAHGEGNYYCDDETLARLQKNNQIVFRYASGGNPNGSVHDIAGICSERGNVVGMMPHPERAVSQLLGSEDGKRMFTSILNAWREQHDAAVNS
>NZ_CP045802|4966897:4976580|4968665_4970132_-|WP_153784797.1|DBSCAN-SWA
MRAVSRAWEDAHYNAGIGRDDIFDKLKEECGVFGVFGTPDASSLAYYGLHALQHRGEESSGVCTVDSATGGFAYHRGMGLVKEVFTSDILASLPGDRAIGHVRYSTSGASQLGNAQPLVFKYRDGDLAVATNGNIVNAPSIRRELESMGSIFQTTSDTEVIAHLIARSPKDFVSAARDALRRIVGGFAFLIMTNERLLVASDTNGLRPLVMGRLGDGYVFASETCAFETIGAEYVRDVQPGELLILDADGLREERFDEEERRASCAMEYIYFARPDSDINEVNIHTARKQMGRRLAVEAFVDADIVVGVPDSSISAAIGYAEQTGIPYEMGLIKNKYSGRTFIQPSQELREKGVKMKLSAVRKIVQGKRVVMIDDSIVRGTTSLRIVNMLREAGAAEVHVRISSPPFANPCYYGIDTPDRRELIASSKTVEEIREAINADSLYFLSAEGLIESASVPGDSKGGGLCLACFNNDYPTPVDESSDKSCSC
>NZ_CP045802|4966897:4976580|4967592_4968636_-|WP_153784290.1|DBSCAN-SWA
MAEAYKQAGVDIAAGNEAVERMKKHVKRTIRPEVLGGLGGFGGLFSLDKNKYEEPVLVSGTDGVGTKLMLAFAMDKHDTIGIDAVAMCVNDIIVQGAEPLFFLDYLATGKVEPEKIEQIVAGIAEGCVQAGCALIGGETAEMPGMYTPEEYDIGGFTVGVVDRAKMIDGSAIAPGDAVIGLASSGIHSNGYSLVRRLLLEQAGYGLQDELAELGGKRLGDVLLEPTRIYVKPALELIGKVQVKGMAHITGGGFIENIPRVLPEGVNVEVAFGSWPIQPIFKLLQDKGSITNRDMFTTFNMGIGLVVVVPADEAEAALAALAELGEQAYRIGAVTEGSRIVTFTGADV
>NZ_CP045802|4966897:4976580|4975284_4976580_-|WP_153784292.1|DBSCAN-SWA
MLERYSRPEMRAIWTEENKFKAWLEVELCACEAWAELGVIPREDVAALREKAGFDIDRISEIELETRHDVIAFTRAVSETLGPERKWVHYGLTSTDVVDTATGYLLRQANEILERDVVNFIEILRGQAVAYKDTVMMGRTHGVHAEPTTFGLKLALWYEEMKRNLERFRHAADGVQYGKISGAVGTYANIDPFVEEFVCRKLGTKPAPISTQTLQRDRHAEYMATLALIATSLDKFATEIRALQKSEFREVEEPFAKGQKGSSAMPHKRNPIGCENISGLARVIRGHMISAYENVPLWHERDISHSSVERVILPDATMLLNYMLNRLGNIIKNLQVFPDNMKRNMGRTFGVPFSGRVMTMLIDKGFSREQAYDTVQPRAMQAWEEQRQFRDIIAETPEITAALSAQEIDDAFNPSWHLKHVDTIFRRLELI
>NZ_CP045802|4966897:4976580|4966897_4967593_-|WP_153784289.1|DBSCAN-SWA
MAEQLRFDLGDGDRTGGQLRVAVFASGQGSNFQALADAAADGKLGGSIELLVCDRAEAPVVGRARRAGIDAWVFDPKAYASREAYEGEILAELQRRGVGLVVLAGYMRILTPVLVDAYAGRMINIHPSLLPAFPGMHAIRQALNYGVKVTGVTIHFVDGGLDSGPIIAQRALEIGEGESEASLAERIHAAENALYPWAVRGFAEGRISLDGRRALVSADAGAGADDDSADK

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_153784289.1|4966897_4967593_-	phosphoribosylglycinamide formyltransferase	M4QRX9	Synechococcus_phage	4.3e-24	36.6
WP_153784290.1|4967592_4968636_-	phosphoribosylformylglycinamidine cyclo-ligase	Q58MH8	Prochlorococcus_phage	8.2e-72	46.5
WP_153784797.1|4968665_4970132_-	amidophosphoribosyltransferase	A0A0M3SGR2	Mollivirus	1.7e-51	32.4
WP_153784291.1|4970278_4972528_-	phosphoribosylformylglycinamidine synthase subunit PurL	A6N228	Microbacterium_phage	1.1e-156	42.2
WP_028598682.1|4972505_4973201_-	phosphoribosylformylglycinamidine synthase subunit PurQ	NA	NA	NA	NA
WP_028598681.1|4973205_4973448_-	phosphoribosylformylglycinamidine synthase subunit PurS	A0A0E3FJ99	Synechococcus_phage	2.8e-07	35.1
WP_028598680.1|4974261_4975161_-	phosphoribosylaminoimidazolesuccinocarboxamide synthase	A0A0M4JBD3	Mollivirus	1.6e-39	34.5
WP_153784292.1|4975284_4976580_-	adenylosuccinate lyase	A0A2H4UUU6	Bodo_saltans_virus	2.8e-21	26.5